WO2009119688A1 - Sealing material for liquid-crystal dropping process, vertical-conduction material, and liquid-crystal display element - Google Patents
Sealing material for liquid-crystal dropping process, vertical-conduction material, and liquid-crystal display element Download PDFInfo
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- WO2009119688A1 WO2009119688A1 PCT/JP2009/056002 JP2009056002W WO2009119688A1 WO 2009119688 A1 WO2009119688 A1 WO 2009119688A1 JP 2009056002 W JP2009056002 W JP 2009056002W WO 2009119688 A1 WO2009119688 A1 WO 2009119688A1
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1339—Gaskets; Spacers; Sealing of cells
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1438—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing oxygen
- C08G59/1455—Monocarboxylic acids, anhydrides, halides, or low-molecular-weight esters thereof
- C08G59/1461—Unsaturated monoacids
- C08G59/1466—Acrylic or methacrylic acids
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
- C09J163/10—Epoxy resins modified by unsaturated compounds
Definitions
- the present invention is a liquid crystal that is excellent in coating properties, has high adhesion between a seal and a substrate, and hardly causes liquid crystal contamination, and is optimal for manufacturing a liquid crystal display element with little color unevenness in liquid crystal display.
- the present invention relates to a sealing agent for dripping method.
- this invention relates to the vertical conduction material and liquid crystal display element which use this sealing compound for liquid crystal dropping methods.
- a liquid crystal display element such as a liquid crystal display cell forms a cell by facing two transparent substrates with electrodes facing each other at a predetermined interval and sealing the periphery with a sealing agent made of a curable resin composition.
- a sealing agent made of a curable resin composition.
- it was produced by injecting liquid crystal into the cell from a liquid crystal injection port provided in a part thereof, and sealing the liquid crystal injection port with a sealing agent or a sealing agent.
- a seal pattern provided with a liquid crystal injection port is formed on one of two transparent substrates with electrodes using a thermosetting sealant, and prebaked at 60 to 100 ° C. in the sealant. Dry the solvent.
- the two substrates are placed facing each other with a spacer in between and bonded, and hot pressing is performed at 110 to 220 ° C. for 10 to 90 minutes to adjust the gap near the seal, and then in an oven at 110 to 220 ° C. Heat for 10 to 120 minutes to fully cure the sealant.
- liquid crystal was injected from the liquid crystal injection port, and finally, the liquid crystal injection port was sealed using a sealing agent to produce a liquid crystal display element.
- thermal distortion causes positional deviation, gap variation, decrease in adhesion between the sealing agent and the substrate, etc.
- residual solvent thermally expands, bubbles are generated, cap variation and seal path are
- problems such as generation of a seal, a long seal curing time, a complicated pre-baking process, a short usable time of the sealant due to volatilization of the solvent, and a long time for liquid crystal injection.
- a large liquid crystal display device in recent years it takes a very long time to inject liquid crystal.
- the manufacturing method of the liquid crystal display element called the dripping method using the sealing agent which consists of a photocurable thermosetting combined type resin composition is examined (for example, refer patent document 1).
- the dropping method first, a rectangular seal pattern is formed on one of the two transparent substrates with electrodes by screen printing. Next, a liquid crystal micro-droplet is applied to the entire surface of the transparent substrate in an uncured state with the sealant uncured, and the other transparent substrate is stacked under vacuum to return to normal pressure. To temporarily cure. Thereafter, heating is performed at the time of liquid crystal annealing to perform main curing, and a liquid crystal display element is manufactured.
- a liquid crystal display element can be manufactured with extremely high efficiency, and this dropping method is currently the mainstream of the manufacturing method of the liquid crystal display element.
- the liquid crystal dropping method can significantly reduce the liquid crystal introduction process time compared to the vacuum injection method, while the sealant is in contact with the liquid crystal in an uncured state, so the components of the sealant are easily eluted into the liquid crystal.
- As one of the methods for solving such a problem there is a method of performing two-stage curing by ultraviolet rays and heating using a photocuring and thermosetting combined sealing agent. In this two-stage curing, a sealing agent is used. The higher the percentage of photocured is, the more the elution of the sealing agent component into the liquid crystal can be suppressed.
- the photocuring / thermosetting sealant has a problem in that when it is photocured, stress is generated inside the cured product, so that the adhesiveness to the substrate is not sufficient.
- Patent Document 2 describes that the adhesion between the sealing agent and the substrate is increased by adding a (meth) acrylate compound having a structure derived from a cyclic lactone to the sealing agent.
- the sealing agent described in Patent Document 2 has a problem that the viscosity is very high, so that the coating property is inferior, and the sealing agent may break when applied to the substrate. .
- the present invention is a liquid crystal dropping method that is excellent in coating properties, has high adhesion between a seal and a substrate, and hardly causes liquid crystal contamination, and is optimal for manufacturing a liquid crystal display device with little color unevenness in a liquid crystal display.
- An object of the present invention is to provide a sealing agent.
- an object of this invention is to provide the vertical conduction material and liquid crystal display element which use this sealing compound for liquid crystal dropping methods.
- This invention is the sealing compound for liquid crystal dropping methods containing the (meth) acrylate compound which has a structure represented by following General formula (1).
- R 1 represents a hydrogen atom or a methyl group
- R 2 represents the following chemical formula (2-1) or (2-2)
- R 3 represents a structure derived from an acid anhydride
- R 2 4 represents a structure derived from an epoxy compound
- X represents a ring-opening structure of a cyclic lactone
- n represents an integer of 2 to 5
- a represents an integer of 1 to 4.
- b represents an integer of 0 to 8
- c represents an integer of 0 to 3
- d represents an integer of 0 to 8
- e represents an integer of 0 to 8
- Any one of c and d is 1 or more.
- the present inventors have so far proposed a sealing agent for liquid crystal display elements using a curable resin composition containing an acrylated epoxy resin as a suitable sealing agent particularly in the dropping method.
- the sealing agent for liquid crystal display elements can be a combined type of photocuring and thermosetting, and the polarity of the contained resin is high, which is compatible with liquid crystals. Therefore, contamination of the liquid crystal can be effectively prevented.
- a (meth) acrylate compound having a structure derived from a cyclic lactone is further added to such a sealing agent for liquid crystal display elements, or a (meth) acrylate compound having a structure derived from a cyclic lactone instead of an acrylated epoxy resin.
- Patent Document 2 the adhesiveness between the sealing agent and the substrate could be increased.
- the sealing agent for liquid crystal dropping method of the present invention contains a (meth) acrylate compound having a structure represented by the general formula (1).
- the sealing agent of the present invention has an appropriate viscosity and excellent coatability. And the outstanding effect that the adhesiveness of the seal
- (meth) acrylate means acrylate or methacrylate.
- X represents a ring-opening structure of a cyclic lactone.
- the (meth) acrylate compound having the structure represented by the general formula (1) can increase the adhesion between the sealing agent and the substrate.
- the lower limit of n indicating the number of units of X is 2 and the upper limit is 5.
- the molecular weight of the (meth) acrylate compound having the structure represented by the general formula (1) is too small, the number of OH groups per molecule increases, and the intermolecular hydrogen bond strength increases. Since it becomes strong, the viscosity of the resulting sealant becomes too high.
- n exceeds 5
- the OH group per molecule decreases and the intermolecular hydrogen bond strength becomes weak, so the viscosity becomes too low, the synthesis reaction becomes multistage, and the unreacted raw material is added to the target product. Since it remains, the liquid crystal may be contaminated when used as a sealant.
- a preferable upper limit of n is 4.
- the cyclic lactone that forms the ring-opening structure of the cyclic lactone is not particularly limited.
- ⁇ -undecalactone, ⁇ -caprolactone, ⁇ -decalactone, ⁇ -dodecalactone, ⁇ -nonalactone, ⁇ -heptalactone examples thereof include ⁇ -valerolactone, ⁇ -valerolactone, ⁇ -butyrolactone, ⁇ -butyrolactone, ⁇ -propiolactone, ⁇ -hexanolactone, 7-butyl-2-oxepanone and the like.
- These cyclic lactones may be used alone or in combination of two or more. Among them, those having 5 to 7 carbon atoms in the straight chain portion of the main skeleton when the ring is opened are preferable.
- R 2 is represented by the chemical formula (2-2) in which b is 1 to 4, c is 0, and d is 0. Is preferred.
- the (meth) acrylate compound having the structure represented by the general formula (1) is preferably a polyfunctional (meth) acrylate compound having a 2 or more, that is, 2 or more (meth) acryl groups.
- the (meth) acrylate compound is a polyfunctional (meth) acrylate compound having two or more (meth) acryl groups
- the cured product of the sealing agent of the present invention has excellent heat resistance due to an increase in crosslink density. , Become reliable. Especially, it is more preferable that said a is 2.
- the (meth) acrylate (A) can be obtained, for example, by a method in which a (meth) acrylic ester having a hydroxyl group such as 2-hydroxyethyl acrylate and a cyclic lactone are mixed and heated to react. it can.
- a (meth) acrylic ester having a hydroxyl group such as 2-hydroxyethyl acrylate and a cyclic lactone
- Specific examples of the (meth) acrylate (A) include caprolactone-2- (meth) acryloyloxyethyl.
- the cyclic anhydride in (B), R 3 is the same as the R 3 in having a structure represented by the general formula (1) (meth) acrylate compounds, cyclic acids such as the following specific examples
- the acid structure portion is removed from the anhydride.
- Specific examples of the cyclic anhydride (B) include, for example, maleic anhydride, succinic anhydride, phthalic anhydride, citraconic anhydride, Ricacid TH, Jamaicacid HT-1, Jamaicacid HH, Jamaicacid HT-700, Jamaicacid MH, Ricacid MT-500, Jamaicacid HNA, Ricacid HNA-100, Ricacid OSA, Ricacid DDSA (all of which are manufactured by Shin Nippon Rika Co., Ltd.) and the like.
- the (meth) acrylate compound having the structure represented by the general formula (1) can be obtained by reacting the obtained carboxylic acid (C) with an epoxy compound.
- the epoxy compound may be a monofunctional epoxy compound, but is preferably a polyfunctional epoxy compound having two or more epoxy groups.
- the resulting (meth) acrylate compound having a structure represented by the general formula (1) is two or more (meth) acrylic compounds. It becomes a polyfunctional (meth) acrylate compound having a group. Specifically, a polyfunctional epoxy group having two or more (meth) acryl groups by reacting 1 mol of the polyfunctional epoxy with a carboxylic acid (C) having the number of moles corresponding to the number of epoxy groups of the polyfunctional epoxy. A (meth) acrylate compound is obtained. At this time, the number of (meth) acryl groups of the (meth) acrylate compound having the structure represented by the general formula (1) to be obtained is the same as the number of epoxy groups of the used polyfunctional epoxy.
- the monofunctional epoxy compound examples include Licarresin L-100 (manufactured by Shin Nippon Rika Co., Ltd.), EPICLON 520, EPICLON 703 (all of which are manufactured by DIC), n-butyl glycidyl ether, glycidyl (meth) acrylate, Examples thereof include 4-hydroxybutyl acrylate glycidyl, and the number of carbon atoms constituting the main chain is preferably 10 or less.
- bifunctional epoxy compound among the polyfunctional epoxy compounds include, for example, bisphenol types such as EPICLON EXA-850CRP (made by DIC), hydrogenated bisphenol types such as EPICLON EXA-7015 (made by DIC), Examples thereof include ethylene glycol diglycidyl ether, and specific examples of the trifunctional or higher functional epoxy compound include EPICLON 725 (manufactured by DIC).
- bisphenol type and hydrogenated bisphenol type include A type, E type, and F type.
- R 4 in the (meth) acrylate compound having the structure represented by the general formula (1) produced by such a method becomes a structure derived from the epoxy compound, and when the epoxy compound is a polyfunctional epoxy, a is 2 or more.
- the sealing agent of the present invention may contain other curable resins in addition to the (meth) acrylate compound having the structure represented by the general formula (1).
- the preferable minimum of the compounding quantity of the (meth) acrylate compound which has a structure represented by the said General formula (1) in all the curable resin components to contain is 5 weight%, and a preferable upper limit is 80 weight%.
- the blending amount of the (meth) acrylate compound having the structure represented by the general formula (1) is less than 5% by weight, the residual stress of the cured sealant obtained cannot be sufficiently relaxed, and the produced liquid crystal The adhesion between the substrates of the display elements may be insufficient.
- the blending amount of the (meth) acrylate compound having the structure represented by the general formula (1) exceeds 80% by weight, a cured product of the obtained sealing agent is used to disperse the residual stress. Although the adhesiveness between the substrates is enhanced, the workability such as the dispensing property of the obtained sealant may be extremely deteriorated.
- the more preferable lower limit of the blending amount of the (meth) acrylate compound having the structure represented by the general formula (1) is 10% by weight, and the more preferable upper limit is 50% by weight.
- the other curable resin is not particularly limited, and examples thereof include those having a reactive functional group such as a (meth) acryloyl group, a cyclic ether such as an epoxy group or an oxetanyl group, and a styryl group.
- a reactive functional group such as a (meth) acryloyl group, a cyclic ether such as an epoxy group or an oxetanyl group, and a styryl group.
- (meth) acrylic acid ester, partial epoxy (meth) acrylate resin, epoxy resin and the like are suitable.
- Examples of the (meth) acrylic acid ester include an ester compound obtained by reacting a compound having a hydroxyl group with (meth) acrylic acid, and an epoxy obtained by reacting (meth) acrylic acid with an epoxy compound ( Examples thereof include urethane (meth) acrylates obtained by reacting (meth) acrylates and isocyanates with (meth) acrylic acid derivatives having a hydroxyl group.
- the epoxy (meth) acrylate obtained by reacting the (meth) acrylic acid and the epoxy compound is not particularly limited.
- an epoxy resin and (meth) acrylic acid are combined in the presence of a basic catalyst according to a conventional method. What is obtained by reacting with is mentioned.
- Examples of the urethane (meth) acrylate obtained by reacting the above isocyanate with a (meth) acrylic acid derivative having a hydroxyl group include, for example, a (meth) acrylic acid derivative having a hydroxyl group with respect to 1 equivalent of a compound having two isocyanate groups. Two equivalents can be obtained by reacting in the presence of a catalytic amount of a tin-based compound.
- Examples of the partial epoxy (meth) acrylate resin include a compound obtained by reacting a partial epoxy group of a compound having two or more epoxy groups with (meth) acrylic acid, or a hydroxyl group in a bifunctional or higher isocyanate. And a compound obtained by reacting a (meth) acrylic acid derivative having glycidol and then glycidol.
- the epoxy resin is not particularly limited, and examples thereof include epichlorohydrin derivatives, cycloaliphatic epoxy resins, compounds obtained from the reaction of isocyanate and glycidol, and the like.
- the other curable resin is preferably a compound having two or more reactive groups in one molecule in order to reduce the uncured residue at the time of curing as much as possible.
- the other curable resin preferably has at least one hydrogen-bonding functional group in one molecule in order to further suppress the elution of the uncured sealing agent of the present invention into the liquid crystal.
- the hydrogen bonding functional group is not particularly limited, and examples thereof include an —OH group, —SH group, —NHR group (R represents an aromatic or aliphatic hydrocarbon, and derivatives thereof), —COOH group , Functional groups such as —NHOH groups, and residues such as —NHCO—, —NH—, —CONHCO—, —NH—NH—, etc. present in the molecule.
- An OH group is preferred.
- the sealing agent of the present invention preferably contains a photopolymerization initiator.
- the photopolymerization initiator is not particularly limited, and for example, benzophenone compounds, acetophenone compounds, acylphosphine oxide compounds, titanocene compounds, oxime ester compounds, benzoin ether compounds, benzyl, thioxanthone, etc. are suitable. Can be used. These photoinitiators may be used independently and may use 2 or more types together.
- Examples of commercially available photopolymerization initiators include Irgacure 907, Irgacure 819, Irgacure 651, Irgacure 369, Irgacure OXE01 (all of which are manufactured by Ciba Specialty Chemicals), Bensoin Methyl.
- Examples include ether, benzoin ethyl ether, benzoin isopropyl ether, Lucillin TPO (BASF Japan), KR-02 (Light Chemical).
- content of the said photoinitiator is not specifically limited, A preferable minimum with respect to a total of 100 weight part of the (meth) acrylate compound and other curable resin which have a structure represented by General formula (1) mentioned above. Is 0.1 part by weight, and the preferred upper limit is 10 parts by weight. If the content of the photopolymerization initiator is less than 0.1 parts by weight, the ability to start photopolymerization may be insufficient and the above-described effects of the present invention may not be obtained. When content of the said photoinitiator exceeds 10 weight part, many unreacted radical polymerization initiators remain, and the weather resistance of the sealing agent of this invention may worsen.
- the minimum with more preferable content of the said photoinitiator is 1 weight part, and a more preferable upper limit is 5 weight part.
- the sealing agent of the present invention preferably contains a polymerization inhibitor. By containing the said polymerization inhibitor, it can suppress that gelatinization advances after carrying out the vacuum degassing of the sealing agent of this invention.
- the polymerization inhibitor is not particularly limited.
- 2,6-di-t-butylcresol, butylated hydroxyanisole, 2,6-di-t-butyl-4, ethylphenol, stearyl ⁇ - (3,5 -Di-t-butyl-4-hydroxyphenyl) propionate 2,2'-methylenebis (4-methyl-6-t-butylphenol), 2,2'-methylenebis (4-ethyl-6-t-butylphenol), 4,4′-thiobis-3-methyl-6-tert-butylphenol), 4,4-butylidenebis (3-methyl-6-tert-butylphenol), 3,9-bis [1,1-dimethyl-2- [ ⁇ - (3-tert-butyl-4-hydroxy-5-methylphenyl) propionyloxy] ethyl] -2,4,8,10-tetraoxaspiro [5,5] undeca Tetrakis- [methylene-3- (3 ′, 5′
- the content of the polymerization inhibitor is not particularly limited, but the preferable lower limit is 50 ppm and the preferable upper limit is 2000 ppm with respect to the total amount of the sealing agent. If the content of the polymerization inhibitor is less than 50 ppm, gelation proceeds after the resulting sealant composition is degassed in vacuum, and it may be difficult to store and use. When content of the said polymerization inhibitor exceeds 2000 ppm, the photoreactivity of the sealing agent obtained may be suppressed and sclerosis
- the minimum with more preferable content of the said polymerization inhibitor is 70 ppm, and a more preferable upper limit is 1800 ppm.
- thermosetting agent When using together the curable resin which has an epoxy group in the sealing compound of this invention, it is preferable to contain a thermosetting agent.
- thermosetting agent examples include hydrazide compounds such as 1,3-bis [hydrazinocarbonoethyl-5-isopropylhydantoin], dicyandiamide, guanidine derivatives, 1-cyanoethyl-2-phenylimidazole, N- [2- (2-Methyl-1-imidazolyl) ethyl] urea, 2,4-diamino-6- [2′-methylimidazolyl- (1 ′)]-ethyl-s-triazine, N, N′-bis (2-methyl -1-imidazolylethyl) urea, N, N ′-(2-methyl-1-imidazolylethyl) -adipamide, 2-phenyl-4-methyl-5-hydroxymethylimidazole, 2-phenyl-4,5-dihydroxymethyl Imidazole derivatives such as imidazole, modified aliphatic polyamines, tetrahydrophthalic anhydride, ethylene
- the compounding quantity of the said thermosetting agent is not specifically limited, A preferable minimum is 0 with respect to a total of 100 weight part of the (meth) acrylate compound which has a structure represented by the said General formula (1), and other curable resin. .1 part by weight, the preferred upper limit is 50 parts by weight.
- the blending amount of the thermosetting agent is less than 0.1 parts by weight, the curable resin having an epoxy group may not be sufficiently cured.
- the blending amount of the thermosetting agent exceeds 50 parts by weight, the moisture resistance of the cured product may be lowered.
- a more preferable lower limit of the amount of the thermosetting agent is 1 part by weight, and a more preferable upper limit is 20 parts by weight.
- the sealing agent of the present invention may contain a silane coupling agent.
- the silane coupling agent mainly serves as an adhesion assistant that improves the adhesion between the sealing agent of the present invention and the substrate.
- the silane coupling agent is not particularly limited, but is excellent in the effect of improving the adhesion to the substrate and can be prevented from flowing into the liquid crystal material by chemically bonding with the curable resin.
- Propyltrimethoxysilane, ⁇ -mercaptopropyltrimethoxysilane, ⁇ -glycidoxypropyltrimethoxysilane, ⁇ -isocyanatopropyltrimethoxysilane and the like are preferably used.
- These silane coupling agents may be used alone or in combination of two or more.
- the sealing agent of the present invention may contain a filler for the purpose of improving the adhesiveness due to the stress dispersion effect and improving the linear expansion coefficient.
- the filler is not particularly limited, for example, talc, asbestos, silica, diatomaceous earth, smectite, bentonite, calcium carbonate, magnesium carbonate, alumina, montmorillonite, diatomaceous earth, zinc oxide, iron oxide, magnesium oxide, tin oxide, titanium oxide, Inorganic fillers such as magnesium hydroxide, aluminum hydroxide, glass beads, silicon nitride, barium sulfate, gypsum, calcium silicate, talc, glass beads, sericite activated clay, bentonite, aluminum nitride, polyester fine particles, polyurethane fine particles, vinyl heavy Organic fillers such as coalesced fine particles and acrylic polymer fine particles can be mentioned.
- the sealing agent of the present invention further comprises a reactive diluent for adjusting the viscosity, a thixotropic agent for adjusting the thixotropy, a spacer such as a polymer bead for adjusting the panel gap, and 3-P-chlorophenyl as necessary.
- a curing accelerator such as 1,1-dimethylurea, an antifoaming agent, a leveling agent, and other additives may be contained.
- the sealing agent of the present invention includes, for example, a three-roll, etc. (meth) acrylate compound having a structure represented by the above general formula (1), other curable resins and additives blended as necessary. It can be obtained by a method of mixing and uniformly dispersing by a conventionally known method using
- the preferable lower limit of the viscosity when the sealing agent of the present invention is applied to the substrate by dispensing is 200,000 mPa ⁇ s
- the preferable upper limit is 400,000 mPa ⁇ s. If the viscosity is less than 200,000 mPa ⁇ s, the viscosity may be too low, and the applied sealing agent may be pushed by the liquid crystal and the shape may collapse. When the viscosity exceeds 400,000 mPa ⁇ s, the coating property is inferior, and the sealant may break when applied to the substrate.
- the sealing agent of the present invention has an appropriate viscosity in the production of a liquid crystal display element, it has excellent coating properties and can be applied without disconnection. Further, since it has excellent adhesion to the substrate and hardly causes liquid crystal contamination, it can be suitably used for the production of a liquid crystal display element with little color unevenness in liquid crystal display.
- a vertical conduction material can be produced by blending conductive fine particles with the liquid crystal dropping method sealing agent of the present invention. If such a vertical conduction material is used, the electrodes of the substrate can be reliably conductively connected.
- the vertical conduction material containing the sealing agent for liquid crystal dropping method of the present invention and conductive fine particles is also one aspect of the present invention.
- the conductive fine particles are not particularly limited, and, for example, metal balls, those obtained by forming a conductive metal layer on the surface of resin fine particles, and the like can be used.
- the one in which the conductive metal layer is formed on the surface of the resin fine particles is preferable because the conductive connection is possible without damaging the substrate or the like due to the excellent elasticity of the resin fine particles.
- the method for producing a liquid crystal display element using the sealing agent of the present invention and / or the vertical conduction material of the present invention is not particularly limited, and for example, it can be produced by a conventionally known method.
- a liquid crystal display element using the sealing agent of the present invention and / or the vertical conduction material of the present invention is also one aspect of the present invention.
- a liquid crystal that is excellent in coating properties, has high adhesion between a seal and a substrate, and hardly causes liquid crystal contamination, so that it is optimal for manufacturing a liquid crystal display element with little color unevenness in liquid crystal display. It is possible to provide a sealing agent for dropping method, a vertical conduction material, and a liquid crystal display element.
- Examples 1 to 15, Comparative Examples 1 to 7 were prepared by stirring the raw materials in the blending amounts shown in Tables 1 to 3 with a planetary stirrer (“Shinky Co., Ltd.”, “Awatori Netaro”) and then uniformly mixing them with a three-roll ceramic roll. The sealing agents for the liquid crystal dropping method of Comparative Examples 1 to 7 were obtained.
- a planetary stirrer (“Shinky Co., Ltd.”, “Awatori Netaro”)
- the sealing agents for the liquid crystal dropping method of Comparative Examples 1 to 7 were obtained.
- As raw materials in the table other than the curable resins A to M synthesized above “KR-02” manufactured by Light Chemical Co., Ltd. is used as a photopolymerization initiator, and “EBECRYL 3700” manufactured by Daicel Cytec Co., Ltd. is used as a bisphenol A type epoxy acrylate resin.
- silane coupling agent “KBM403” manufactured by Shin-Etsu Chemical Co., Ltd., “SO-C1” manufactured by Admatechs Corporation as the silica, and malonic acid dihydrazide or sebacic acid dihydrazide were used as the thermosetting agent.
- liquid droplets manufactured by Chisso Co., Ltd., “JC-5004LA”
- JC-5004LA liquid droplets
- a metal halide lamp was used for the agent part, and 100 mW / cm 2 of ultraviolet rays were irradiated for 30 seconds to prepare 20 evaluation panels.
- the number of defective panels due to disconnection and the number of defective panels due to liquid crystal leakage from the inside of the panel were counted and evaluated according to the following criteria.
- ⁇ Number of defective panels 0: Number of defective panels 1 to 2
- ⁇ Number of defective panels 3 to 5
- substrate 6 which vapor-deposited the whole surface were prepared.
- Each sealing agent was applied in the form of dots on the boundary between the portions of the substrate 5 where the chromium was not deposited, and the substrates 6 were bonded together and then crushed sufficiently.
- the substrates 5 and 6 are peeled off, washed with toluene, and the portion where the seal remains without being washed. This distance was measured using a microscope.
- the coating property is excellent, the adhesiveness between the seal and the substrate is high, and the liquid crystal is hardly contaminated.
- a sealing agent for a certain liquid crystal dropping method, a vertical conduction material, and a liquid crystal display element can be provided.
Abstract
Description
このような問題を解決するための方法の1つとして、光硬化熱硬化併用型シール剤を用いて、紫外線と加熱とによる二段階硬化を行う方法が挙げられ、この二段階硬化において、シール剤が光硬化した割合が大きければ大きいほど、シール剤成分の液晶への溶出を抑えることができる。
しかしながら、光硬化熱硬化併用型シール剤は、光硬化すると硬化物の内部に応力が生じるため基板との接着性が充分でないという問題があった。 The liquid crystal dropping method can significantly reduce the liquid crystal introduction process time compared to the vacuum injection method, while the sealant is in contact with the liquid crystal in an uncured state, so the components of the sealant are easily eluted into the liquid crystal. There was a problem of causing liquid crystal contamination.
As one of the methods for solving such a problem, there is a method of performing two-stage curing by ultraviolet rays and heating using a photocuring and thermosetting combined sealing agent. In this two-stage curing, a sealing agent is used. The higher the percentage of photocured is, the more the elution of the sealing agent component into the liquid crystal can be suppressed.
However, the photocuring / thermosetting sealant has a problem in that when it is photocured, stress is generated inside the cured product, so that the adhesiveness to the substrate is not sufficient.
しかしながら、特許文献2に記載されたシール剤は、粘度が非常に高いことから塗工性に劣り、基板に塗工する際にシール剤の断線が発生してしまうことがあるという問題があった。 On the other hand,
However, the sealing agent described in
以下に本発明を詳述する。 In the formula (2-2), b represents an integer of 0 to 8, c represents an integer of 0 to 3, d represents an integer of 0 to 8, e represents an integer of 0 to 8, b, Any one of c and d is 1 or more.
The present invention is described in detail below.
このような硬化性樹脂組成物を用いた場合、液晶表示素子用シール剤を光硬化と熱硬化との併用タイプとすることができるとともに、含有される樹脂の極性が高く、液晶との相溶性が低いことから、液晶の汚染を効果的に防止することができる。このような液晶表示素子用シール剤に、更に環状ラクトン由来の構造を有する(メタ)アクリレート化合物を添加する、又は、アクリル化エポキシ樹脂の代わりに環状ラクトン由来の構造を有する(メタ)アクリレート化合物を用いることで、シール剤と基板の接着性を上昇させることができた(特許文献2)。 The present inventors have so far proposed a sealing agent for liquid crystal display elements using a curable resin composition containing an acrylated epoxy resin as a suitable sealing agent particularly in the dropping method.
When such a curable resin composition is used, the sealing agent for liquid crystal display elements can be a combined type of photocuring and thermosetting, and the polarity of the contained resin is high, which is compatible with liquid crystals. Therefore, contamination of the liquid crystal can be effectively prevented. A (meth) acrylate compound having a structure derived from a cyclic lactone is further added to such a sealing agent for liquid crystal display elements, or a (meth) acrylate compound having a structure derived from a cyclic lactone instead of an acrylated epoxy resin. By using it, the adhesiveness between the sealing agent and the substrate could be increased (Patent Document 2).
なお、本明細書において、(メタ)アクリレートとは、アクリレート又はメタクリレートを意味する。 The sealing agent for liquid crystal dropping method of the present invention (hereinafter also simply referred to as the sealing agent of the present invention) contains a (meth) acrylate compound having a structure represented by the general formula (1). By containing such a (meth) acrylate compound, the sealing agent of the present invention has an appropriate viscosity and excellent coatability. And the outstanding effect that the adhesiveness of the seal | sticker after hardening and a board | substrate is high can be exhibited.
In the present specification, (meth) acrylate means acrylate or methacrylate.
上記Xのユニット数を示すnの下限は2、上限は5である。上記nが2未満であると、上記一般式(1)で表される構造を有する(メタ)アクリレート化合物の分子量が小さすぎて、1分子あたりのOH基が多くなって分子間水素結合力が強くなることから、得られるシール剤の粘度が高くなりすぎる。上記nが5を超えると、1分子あたりのOH基が少なくなって分子間水素結合力が弱くなることから粘度が低くなりすぎたり、合成反応が多段になり、目的生成物に未反応原料が残存してしまうため、シール剤としたときに液晶を汚染したりすることがある。上記nの好ましい上限は4である。 In the general formula (1), X represents a ring-opening structure of a cyclic lactone. By having such a ring-opening structure of a cyclic lactone in the molecule, the (meth) acrylate compound having the structure represented by the general formula (1) can increase the adhesion between the sealing agent and the substrate.
The lower limit of n indicating the number of units of X is 2 and the upper limit is 5. When the n is less than 2, the molecular weight of the (meth) acrylate compound having the structure represented by the general formula (1) is too small, the number of OH groups per molecule increases, and the intermolecular hydrogen bond strength increases. Since it becomes strong, the viscosity of the resulting sealant becomes too high. When n exceeds 5, the OH group per molecule decreases and the intermolecular hydrogen bond strength becomes weak, so the viscosity becomes too low, the synthesis reaction becomes multistage, and the unreacted raw material is added to the target product. Since it remains, the liquid crystal may be contaminated when used as a sealant. A preferable upper limit of n is 4.
なかでも、開環したときに主骨格の直鎖部分の炭素数が5~7となるものが好適である。 The cyclic lactone that forms the ring-opening structure of the cyclic lactone is not particularly limited. For example, γ-undecalactone, ε-caprolactone, γ-decalactone, σ-dodecalactone, γ-nonalactone, γ-heptalactone, Examples thereof include γ-valerolactone, σ-valerolactone, β-butyrolactone, γ-butyrolactone, β-propiolactone, σ-hexanolactone, 7-butyl-2-oxepanone and the like. These cyclic lactones may be used alone or in combination of two or more.
Among them, those having 5 to 7 carbon atoms in the straight chain portion of the main skeleton when the ring is opened are preferable.
上記(メタ)アクリレート(A)において、R1、R2、及びXは、上記一般式(1)で表される構造を有する(メタ)アクリレート化合物におけるR1、R2、及びXと同様のものである。 In the reaction formula (3), the (meth) acrylate (A) and the cyclic anhydride (B) are reacted to obtain the carboxylic acid (C).
In the (meth) acrylate (A), R 1, R 2, and X has a structure represented by the above general formula (1) (meth) in the acrylate compound R 1, R 2, and similar to the X Is.
上記(メタ)アクリレート(A)の具体例としては、例えば、カプロラクトン-2-(メタ)アクリロイルオキシエチル等が挙げられる。 The (meth) acrylate (A) can be obtained, for example, by a method in which a (meth) acrylic ester having a hydroxyl group such as 2-hydroxyethyl acrylate and a cyclic lactone are mixed and heated to react. it can.
Specific examples of the (meth) acrylate (A) include caprolactone-2- (meth) acryloyloxyethyl.
上記環状の無水物(B)の具体例としては、例えば、無水マレイン酸、無水コハク酸、無水フタル酸、無水シトラコン酸や、リカシッドTH、リカシッドHT-1、リカシッドHH、リカシッドHT-700、リカシッドMH、リカシッドMT-500、リカシッドHNA、リカシッドHNA-100、リカシッドOSA、リカシッドDDSA(以上、いずれも新日本理化社製)等が挙げられる。 The cyclic anhydride in (B), R 3 is the same as the R 3 in having a structure represented by the general formula (1) (meth) acrylate compounds, cyclic acids such as the following specific examples The acid structure portion is removed from the anhydride.
Specific examples of the cyclic anhydride (B) include, for example, maleic anhydride, succinic anhydride, phthalic anhydride, citraconic anhydride, Ricacid TH, Ricacid HT-1, Ricacid HH, Ricacid HT-700, Ricacid MH, Ricacid MT-500, Ricacid HNA, Ricacid HNA-100, Ricacid OSA, Ricacid DDSA (all of which are manufactured by Shin Nippon Rika Co., Ltd.) and the like.
上記エポキシ化合物としては、単官能エポキシ化合物であってもよいが、2以上のエポキシ基を有する多官能エポキシ化合物であることが好ましい。 The (meth) acrylate compound having the structure represented by the general formula (1) can be obtained by reacting the obtained carboxylic acid (C) with an epoxy compound.
The epoxy compound may be a monofunctional epoxy compound, but is preferably a polyfunctional epoxy compound having two or more epoxy groups.
上記多官能エポキシ化合物のうち2官能エポキシ化合物としては、具体的には例えば、EPICLON EXA-850CRP(DIC社製)等のビスフェノール型、EPICLON EXA-7015(DIC社製)等の水添ビスフェノール型、エチレングリコールジグリシジルエーテル等が挙げられ、3官能以上のエポキシ化合物としては、具体的には例えば、EPICLON 725(DIC社製)等が挙げられる。また、上記ビスフェノール型、水添ビスフェノール型としては、例えば、A型、E型、F型等が挙げられる。 Specific examples of the monofunctional epoxy compound include Licarresin L-100 (manufactured by Shin Nippon Rika Co., Ltd.), EPICLON 520, EPICLON 703 (all of which are manufactured by DIC), n-butyl glycidyl ether, glycidyl (meth) acrylate, Examples thereof include 4-hydroxybutyl acrylate glycidyl, and the number of carbon atoms constituting the main chain is preferably 10 or less.
Specific examples of the bifunctional epoxy compound among the polyfunctional epoxy compounds include, for example, bisphenol types such as EPICLON EXA-850CRP (made by DIC), hydrogenated bisphenol types such as EPICLON EXA-7015 (made by DIC), Examples thereof include ethylene glycol diglycidyl ether, and specific examples of the trifunctional or higher functional epoxy compound include EPICLON 725 (manufactured by DIC). Examples of the bisphenol type and hydrogenated bisphenol type include A type, E type, and F type.
その場合、含有する全ての硬化性樹脂成分に占める上記一般式(1)で表される構造を有する(メタ)アクリレート化合物の配合量の好ましい下限は5重量%、好ましい上限は80重量%である。上記一般式(1)で表される構造を有する(メタ)アクリレート化合物の配合量が5重量%未満であると、得られるシール剤の硬化物の残留応力を充分に緩和しきれず、製造した液晶表示素子の基板間の接着性が不充分となることがある。上記一般式(1)で表される構造を有する(メタ)アクリレート化合物の配合量が80重量%を超えると、得られるシール剤の硬化物は、残留応力を分散させるため製造する液晶表示素子の基板間の接着性を高めるが、得られるシール剤のディスペンス性等の作業性が非常に悪くなってしまうことがある。上記一般式(1)で表される構造を有する(メタ)アクリレート化合物の配合量のより好ましい下限は10重量%、より好ましい上限は50重量%である。 The sealing agent of the present invention may contain other curable resins in addition to the (meth) acrylate compound having the structure represented by the general formula (1).
In that case, the preferable minimum of the compounding quantity of the (meth) acrylate compound which has a structure represented by the said General formula (1) in all the curable resin components to contain is 5 weight%, and a preferable upper limit is 80 weight%. . When the blending amount of the (meth) acrylate compound having the structure represented by the general formula (1) is less than 5% by weight, the residual stress of the cured sealant obtained cannot be sufficiently relaxed, and the produced liquid crystal The adhesion between the substrates of the display elements may be insufficient. When the blending amount of the (meth) acrylate compound having the structure represented by the general formula (1) exceeds 80% by weight, a cured product of the obtained sealing agent is used to disperse the residual stress. Although the adhesiveness between the substrates is enhanced, the workability such as the dispensing property of the obtained sealant may be extremely deteriorated. The more preferable lower limit of the blending amount of the (meth) acrylate compound having the structure represented by the general formula (1) is 10% by weight, and the more preferable upper limit is 50% by weight.
上記その他の硬化性樹脂は、未硬化の本発明のシール剤の液晶への成分溶出をより抑制するために、1分子中に少なくとも1つ以上の水素結合性官能基を有することが好ましい。
上記水素結合性官能基としては特に限定されず、例えば、-OH基、-SH基、-NHR基(Rは、芳香族又は脂肪族炭化水素、及び、これらの誘導体を表す)、-COOH基、-NHOH基等の官能基、また、分子内に存在する-NHCO-、-NH-、-CONHCO-、-NH-NH-等の残基が挙げられ、なかでも、導入の容易さから-OH基であることが好ましい。 The other curable resin is preferably a compound having two or more reactive groups in one molecule in order to reduce the uncured residue at the time of curing as much as possible.
The other curable resin preferably has at least one hydrogen-bonding functional group in one molecule in order to further suppress the elution of the uncured sealing agent of the present invention into the liquid crystal.
The hydrogen bonding functional group is not particularly limited, and examples thereof include an —OH group, —SH group, —NHR group (R represents an aromatic or aliphatic hydrocarbon, and derivatives thereof), —COOH group , Functional groups such as —NHOH groups, and residues such as —NHCO—, —NH—, —CONHCO—, —NH—NH—, etc. present in the molecule. An OH group is preferred.
上記光重合開始剤としては特に限定されないが、例えば、ベンゾフェノン系化合物、アセトフェノン系化合物、アシルフォスフィンオキサイド系化合物、チタノセン系化合物、オキシムエステル系化合物、ベンゾインエーテル系化合物、ベンジル、チオキサントン等を好適に用いることができる。これらの光重合開始剤は単独で用いてもよく、2種以上を併用してもよい。 The sealing agent of the present invention preferably contains a photopolymerization initiator.
The photopolymerization initiator is not particularly limited, and for example, benzophenone compounds, acetophenone compounds, acylphosphine oxide compounds, titanocene compounds, oxime ester compounds, benzoin ether compounds, benzyl, thioxanthone, etc. are suitable. Can be used. These photoinitiators may be used independently and may use 2 or more types together.
上記重合禁止剤を含有することにより、本発明のシール剤を真空脱泡した後にゲル化が進行することを抑制できる。 The sealing agent of the present invention preferably contains a polymerization inhibitor.
By containing the said polymerization inhibitor, it can suppress that gelatinization advances after carrying out the vacuum degassing of the sealing agent of this invention.
上記シランカップリング剤としては特に限定されないが、基板との接着性向上効果に優れ、硬化性樹脂と化学結合することにより液晶材料中への流出を防止することができることから、例えば、γ-アミノプロピルトリメトキシシラン、γ-メルカプトプロピルトリメトキシシラン、γ-グリシドキシプロピルトリメトキシシラン、γ-イソシアネートプロピルトリメトキシシラン等が好適に用いられる。これらのシランカップリング剤は単独で用いてもよく、2種以上を併用してもよい。 The sealing agent of the present invention may contain a silane coupling agent. The silane coupling agent mainly serves as an adhesion assistant that improves the adhesion between the sealing agent of the present invention and the substrate.
The silane coupling agent is not particularly limited, but is excellent in the effect of improving the adhesion to the substrate and can be prevented from flowing into the liquid crystal material by chemically bonding with the curable resin. Propyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-isocyanatopropyltrimethoxysilane and the like are preferably used. These silane coupling agents may be used alone or in combination of two or more.
本発明の液晶滴下工法用シール剤と導電性微粒子とを含有する上下導通材料もまた、本発明の1つである。 A vertical conduction material can be produced by blending conductive fine particles with the liquid crystal dropping method sealing agent of the present invention. If such a vertical conduction material is used, the electrodes of the substrate can be reliably conductively connected.
The vertical conduction material containing the sealing agent for liquid crystal dropping method of the present invention and conductive fine particles is also one aspect of the present invention.
本発明のシール剤及び/又は本発明の上下導通材料を用いてなる液晶表示素子もまた、本発明の1つである。 The method for producing a liquid crystal display element using the sealing agent of the present invention and / or the vertical conduction material of the present invention is not particularly limited, and for example, it can be produced by a conventionally known method.
A liquid crystal display element using the sealing agent of the present invention and / or the vertical conduction material of the present invention is also one aspect of the present invention.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とβ-プロピオラクトン144重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Aを得た。 (Synthesis of curable resin A)
To the reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 144 parts by weight of β-propiolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Subsequently, 170 parts by weight of bisphenol A diglycidyl ether was added, and the resulting mixture was stirred at 90 ° C. for 5 hours to obtain a curable resin A.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とβ-プロピオラクトン360重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Bを得た。 (Synthesis of curable resin B)
Into the reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 360 parts by weight of β-propiolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Subsequently, 170 parts by weight of bisphenol A diglycidyl ether was added and the resulting mixture was stirred at 90 ° C. for 5 hours to obtain a curable resin B.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とγ-バレロラクトン200重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Cを得た。 (Synthesis of curable resin C)
To the reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 200 parts by weight of γ-valerolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Subsequently, 170 parts by weight of bisphenol A diglycidyl ether was added and the resulting mixture was stirred at 90 ° C. for 5 hours to obtain a curable resin C.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とγ-バレロラクトン500重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Dを得た。 (Synthesis of curable resin D)
In a reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 500 parts by weight of γ-valerolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Subsequently, 170 parts by weight of bisphenol A diglycidyl ether was added and the resulting mixture was stirred at 90 ° C. for 5 hours to obtain a curable resin D.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とε-カプロラクトン114重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Eを得た。 (Synthesis of curable resin E)
Into the reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 114 parts by weight of ε-caprolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Subsequently, 170 parts by weight of bisphenol A diglycidyl ether was added and the resulting mixture was stirred at 90 ° C. for 5 hours to obtain a curable resin E.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とε-カプロラクトン228重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Fを得た。 (Synthesis of curable resin F)
In a reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 228 parts by weight of ε-caprolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Then, 170 weight part of bisphenol A diglycidyl ether was added, and the curable resin F was obtained by stirring at 90 degreeC for 5 hours.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とε-カプロラクトン342重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Gを得た。 (Synthesis of curable resin G)
In a reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 342 parts by weight of ε-caprolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Then, 170 weight part of bisphenol A diglycidyl ether was added, and the curable resin G was obtained by stirring at 90 degreeC for 5 hours.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とε-カプロラクトン456重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Hを得た。 (Synthesis of curable resin H)
Into the reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 456 parts by weight of ε-caprolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Subsequently, 170 parts by weight of bisphenol A diglycidyl ether was added and the resulting mixture was stirred at 90 ° C. for 5 hours to obtain a curable resin H.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とε-カプロラクトン570重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Iを得た。 (Synthesis of curable resin I)
In a reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 570 parts by weight of ε-caprolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Subsequently, 170 parts by weight of bisphenol A diglycidyl ether was added and the resulting mixture was stirred at 90 ° C. for 5 hours to obtain a curable resin I.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とε-カプロラクトン684重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Jを得た。 (Synthesis of curable resin J)
In a reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 684 parts by weight of ε-caprolactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Then, 170 weight part of bisphenol A diglycidyl ether was added, and curable resin J was obtained by stirring at 90 degreeC for 5 hours.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とγ-ヘプタラクトン256重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Kを得た。 (Synthesis of curable resin K)
Into the reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 256 parts by weight of γ-heptalactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Then, 170 weight part of bisphenol A diglycidyl ether was added, and curable resin K was obtained by stirring at 90 degreeC for 5 hours.
反応フラスコに2-ヒドロエキシエチルアクリレート116重量部とγ-ヘプタラクトン640重量部を入れ、重合禁止剤としてハイドロキノン0.3重量部加え、マントルヒーターで90℃に加熱して5時間撹拌した。撹拌生成物に無水フタル酸148重量部を加えてさらに5時間撹拌した。
続いて、ビスフェノールAジグリシジルエーテル170重量部を加え、90℃で5時間撹拌することで硬化性樹脂Lを得た。 (Synthesis of curable resin L)
Into the reaction flask, 116 parts by weight of 2-hydrooxyethyl acrylate and 640 parts by weight of γ-heptalactone were added, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, heated to 90 ° C. with a mantle heater, and stirred for 5 hours. To the stirred product, 148 parts by weight of phthalic anhydride was added and further stirred for 5 hours.
Then, 170 weight part of bisphenol A diglycidyl ether was added, and the curable resin L was obtained by stirring at 90 degreeC for 5 hours.
反応フラスコにアクリル酸72重量部とビスフェノールFジグリシジルエーテル312重量部とを入れ、重合禁止剤としてハイドロキノン0.3重量部加え、反応触媒としてトリエチルアミン0.3重量部を加え、マントルヒーターで90℃に加熱して5時間撹拌し、硬化性樹脂M(部分エポキシアクリレート)を得た。 (Synthesis of curable resin M)
A reaction flask was charged with 72 parts by weight of acrylic acid and 312 parts by weight of bisphenol F diglycidyl ether, 0.3 part by weight of hydroquinone was added as a polymerization inhibitor, 0.3 part by weight of triethylamine was added as a reaction catalyst, and 90 ° C. with a mantle heater. And stirred for 5 hours to obtain a curable resin M (partial epoxy acrylate).
表1~3に記載した配合量の各原料を遊星式攪拌機(シンキー社製、「あわとり練太郎」)にて攪拌した後、セラミック3本ロールにて均一に混合させて実施例1~15、比較例1~7の液晶滴下工法用シール剤を得た。上記で合成した硬化性樹脂A~M以外の表中の原料として、光重合開始剤にはライトケミカル社製「KR-02」、ビスフェノールA型エポキシアクリレート樹脂にはダイセルサイテック社製「EBECRYL 3700」、シランカップリング剤には信越化学工業社製「KBM403」、シリカにはアドマテックス社製「SO-C1」、熱硬化剤にはマロン酸ジヒドラジド又はセバシン酸ジヒドラジドを用いた。 (Examples 1 to 15, Comparative Examples 1 to 7)
Examples 1 to 15 were prepared by stirring the raw materials in the blending amounts shown in Tables 1 to 3 with a planetary stirrer (“Shinky Co., Ltd.”, “Awatori Netaro”) and then uniformly mixing them with a three-roll ceramic roll. The sealing agents for the liquid crystal dropping method of Comparative Examples 1 to 7 were obtained. As raw materials in the table other than the curable resins A to M synthesized above, “KR-02” manufactured by Light Chemical Co., Ltd. is used as a photopolymerization initiator, and “EBECRYL 3700” manufactured by Daicel Cytec Co., Ltd. is used as a bisphenol A type epoxy acrylate resin. As the silane coupling agent, “KBM403” manufactured by Shin-Etsu Chemical Co., Ltd., “SO-C1” manufactured by Admatechs Corporation as the silica, and malonic acid dihydrazide or sebacic acid dihydrazide were used as the thermosetting agent.
実施例1~15、比較例1~7で得られた各シール剤を用いて以下の評価を行った。結果を表1~3に示した。 (Evaluation)
The following evaluations were performed using the sealing agents obtained in Examples 1 to 15 and Comparative Examples 1 to 7. The results are shown in Tables 1-3.
各シール剤を0.5g取り、E型粘度計(BROOK FIELD社製、「DV-III」)に入れ、25℃において回転速度1rpmで測定を行った。 (Measurement of viscosity of sealant)
0.5 g of each sealant was taken, put in an E-type viscometer (manufactured by BROOK FIELD, “DV-III”), and measured at 25 ° C. and a rotation speed of 1 rpm.
得られたそれぞれのシール剤100重量部にスペーサー微粒子(積水化学工業社製、「ミクロパールSI-H050」、5μm)1重量部を分散させてシリンジに充填し、遠心脱泡機(アワトロンAW-1)にて脱泡し、シリンジの吐出圧200kPa、ノズルギャップ42μm、塗布速度80mm/sec、ノズル径が0.4mmφで2枚ガラス基板の一方にディスペンサーで塗布した。続いて液晶(チッソ社製、「JC-5004LA」)の微小滴をガラス基板のシール剤の枠内全面に滴下塗布し、真空下でもう一方のガラス基板を貼り合わせ、10分間放置後、シール剤部分にメタルハライドランプを用いて100mW/cm2の紫外線を30秒照射して評価用パネルを20枚ずつ作製した。各評価用パネルにおいて断線による不良パネルの数とパネル内側からの液晶漏れによる不良パネルの数を数え、以下の基準により評価した。
◎:不良パネル数0枚
○:不良パネル数1~2枚
△:不良パネル数3~5枚
×:不良パネル数5枚以上 (Workability evaluation)
1 part by weight of spacer fine particles (manufactured by Sekisui Chemical Co., Ltd., “Micropearl SI-H050”, 5 μm) is dispersed in 100 parts by weight of each obtained sealing agent and filled into a syringe, and a centrifugal defoamer (Awatron AW- In 1), defoaming was performed, and a syringe discharge pressure of 200 kPa, a nozzle gap of 42 μm, a coating speed of 80 mm / sec, and a nozzle diameter of 0.4 mmφ were applied to one of two glass substrates with a dispenser. Subsequently, liquid droplets (manufactured by Chisso Co., Ltd., “JC-5004LA”) are applied dropwise onto the entire surface of the sealant frame of the glass substrate, and the other glass substrate is bonded together under vacuum, left for 10 minutes, and then sealed. A metal halide lamp was used for the agent part, and 100 mW / cm 2 of ultraviolet rays were irradiated for 30 seconds to prepare 20 evaluation panels. In each evaluation panel, the number of defective panels due to disconnection and the number of defective panels due to liquid crystal leakage from the inside of the panel were counted and evaluated according to the following criteria.
◎: Number of defective panels 0: Number of defective panels 1 to 2 △: Number of
図1に示すように、ガラス基板1(150mm×150mm)に端から30mm内側四方に得られたシール剤2をディスペンスし、ガラス基板3(110mm×110mm)を真空下で重ねて貼り合わせた。紫外線(100mW/cm2、3000mJ)を照射し、続いて120℃で1時間加熱してシール剤を硬化し、接着試験片を得た。
得られた接着試験片の基板の端部を半径5mmの金属棒4を使って5mm/minの速度で押し込んだときに、パネル剥がれが起こる際の強度(Kgf)を測定した。なお、基板が割れてしまうまで押し込んでもパネル剥がれがおきなかった場合は、「割れ」と表現した。 (Board adhesion evaluation)
As shown in FIG. 1, a
When the end of the substrate of the obtained adhesion test piece was pushed in at a speed of 5 mm / min using a
得られたそれぞれのシール剤100重量部にスペーサー微粒子(積水化学工業社製、「ミクロパールSI-H050」、5μm)1重量部を分散させ、シリンジに充填し、遠心脱泡機(アワトロンAW-1)にて脱泡し、シリンジの吐出圧100~400kPa、ノズル径0.4mmφ、ノズルギャップ42μm、塗布速度60mm/secで2枚の配向膜及びITO付き基板の一方にディスペンサーで塗布した。
続いて液晶(チッソ社製、「JC-5004LA」)の微小滴をITO付き基板のシール剤の枠内全面に滴下塗布し、真空下でもう一方のITO付き基板を貼り合わせた。このときシール剤の線幅が約1.5mmになるように各シール剤ごとに吐出圧を調整した。貼り合わせた後、すぐにシール剤部分にメタルハライドランプを用いて100mW/cm2の紫外線を30秒照射して仮硬化した。次いで、120℃で1時間加熱して本硬化を行い、液晶表示パネルを作製した。
得られたそれぞれの液晶表示パネルについて、表示パネル作製直後におけるシール剤付近の液晶配向乱れを目視によって確認した。配向乱れは表示部の色ムラより判断しており、色ムラの程度に応じて、以下の4段階で評価を行った。結果を表1~3に示した。なお、評価が◎、○の液晶パネルは、実用に全く問題のないレベルである。
◎:色むらが全くない
○:色むらが微かにある
△:色むらが少しある
×:色むらがかなりある (Liquid crystal panel evaluation (color unevenness evaluation))
1 part by weight of spacer fine particles (“Micropearl SI-H050”, 5 μm, manufactured by Sekisui Chemical Co., Ltd.) is dispersed in 100 parts by weight of each obtained sealing agent, filled into a syringe, and centrifuged with a centrifugal defoamer (Awatron AW- Defoaming was performed in 1), and applied to one of the two alignment films and the substrate with ITO with a dispenser at a discharge pressure of 100 to 400 kPa, a nozzle diameter of 0.4 mmφ, a nozzle gap of 42 μm, and a coating speed of 60 mm / sec.
Subsequently, fine droplets of liquid crystal (manufactured by Chisso Corporation, “JC-5004LA”) were dropped onto the entire surface of the sealing agent frame of the substrate with ITO, and the other substrate with ITO was bonded together under vacuum. At this time, the discharge pressure was adjusted for each sealing agent so that the line width of the sealing agent was about 1.5 mm. Immediately after bonding, the sealant portion was irradiated with 100 mW / cm 2 of ultraviolet rays for 30 seconds using a metal halide lamp and temporarily cured. Next, main curing was performed by heating at 120 ° C. for 1 hour, and a liquid crystal display panel was produced.
About each obtained liquid crystal display panel, the liquid crystal orientation disorder in the sealant vicinity immediately after display panel preparation was confirmed visually. The alignment disorder was judged from the color unevenness of the display portion, and the evaluation was performed in the following four stages according to the degree of the color unevenness. The results are shown in Tables 1-3. Note that liquid crystal panels with evaluations of ◎ and ○ are at a level where there is no problem in practical use.
◎: No color unevenness ○: Color unevenness is slightly △: Color unevenness is slightly ×: Color unevenness is considerable
表4に記載した配合量の各原料を遊星式攪拌機(シンキー社製、「あわとり練太郎」)にて攪拌した後、セラミック3本ロールにて均一に混合させて参考例1~6の液晶滴下工法用シール剤を得た。上記で合成した硬化性樹脂F及び硬化性樹脂M以外の表中の原料として、光重合開始剤にはライトケミカル社製「KR-02」、ビスフェノールA型エポキシアクリレート樹脂にはダイセルサイテック社製「EBECRYL 3700」、シランカップリング剤には信越化学工業社製「KBM403」、シリカにはアドマテックス社製「SO-C1」、熱硬化剤にはマロン酸ジヒドラジドを用いた。
また、得られた参考例1~6のシール剤中の残存ハイドロキノン量を液体クロマトグラフィーを用いて測定した。結果を表4に示した。なお、参考例1は実施例5と同一のシール剤である。 (Reference Examples 1 to 6)
Each raw material of the blending amounts shown in Table 4 was stirred with a planetary stirrer (“Shinky Co., Ltd.”, “Awatori Netaro”), and then mixed uniformly with three ceramic rolls to obtain the liquid crystals of Reference Examples 1-6. A sealant for the dripping method was obtained. As raw materials in the table other than the curable resin F and curable resin M synthesized above, “KR-02” manufactured by Light Chemical Co., Ltd. is used for the photopolymerization initiator, and Daicel Cytec Co., Ltd. is used for the bisphenol A type epoxy acrylate resin. “EBECRYL 3700”, “KBM403” manufactured by Shin-Etsu Chemical Co., Ltd. was used as the silane coupling agent, “SO-C1” manufactured by Admatechs was used as the silica, and malonic acid dihydrazide was used as the thermosetting agent.
In addition, the amount of residual hydroquinone in the obtained sealants of Reference Examples 1 to 6 was measured using liquid chromatography. The results are shown in Table 4. Reference Example 1 is the same sealant as Example 5.
参考例1~6で得られた各シール剤を用いて以下の評価を行った。
結果を表4に示した。 (Evaluation)
The following evaluations were performed using the sealing agents obtained in Reference Examples 1 to 6.
The results are shown in Table 4.
得られたシール剤をシリンジに入れ、真空脱泡装置(シンキー社製、「ARV-200」)で、1500rpm、3torr、の条件で10分間真空脱泡し、温度23℃、湿度50%で二週間放置し、少量をスパチュラで取り出しガラス基板に手作業で塗布し、シール剤のゲル化が進んでいないかを調べた。ゲル化せず、基板に塗布できたものを「○」、ゲル化して基板にうまく塗布できなかったものを「×」として評価した。 (Evaluation of gelation)
The obtained sealant is put into a syringe and vacuum deaerated for 10 minutes under conditions of 1500 rpm and 3 torr with a vacuum deaerator (“ARV-200”, manufactured by Shinky Corporation). It was left for a week, a small amount was taken out with a spatula and applied to a glass substrate by hand, and it was examined whether or not gelling of the sealant had progressed. Evaluation was made as “◯” for those that did not gel and could be applied to the substrate, and “×” for those that gelled and could not be successfully applied to the substrate.
図2に示すように、コーニングガラス0.7mmtの半面をクロム蒸着した基板5と全面をクロム蒸着した基板6とを準備した。基板5のクロム蒸着した部分としていない部分の境に各シール剤を点状に塗布し、基板6を貼り合わせてから充分に押しつぶした。
次に、貼り合わせた基板に基板5面側から100mW/cm2の紫外線を30秒間照射した後、基板5、6を剥がし、トルエンを用いて洗浄後、洗浄されずにシールが残った部分を硬化したとみなし、この距離をマイクロスコープを用いて測定した。 (Evaluation of light-shielding part curability)
As shown in FIG. 2, the board | substrate 5 which vapor-deposited the half surface of the Corning glass 0.7mmt and the board |
Next, after irradiating the bonded substrate with 100 mW / cm 2 ultraviolet rays from the surface of the substrate 5 for 30 seconds, the
Claims (8)
- 下記一般式(1)で表される構造を有する(メタ)アクリレート化合物を含有することを特徴とする液晶滴下工法用シール剤。
- 一般式(1)中、R2は、bが1~4、cが0、dが0である化学式(2-2)で表されるものであることを特徴とする請求項1記載の液晶滴下工法用シール剤。 2. The liquid crystal according to claim 1, wherein in the general formula (1), R 2 is represented by the chemical formula (2-2) wherein b is 1 to 4, c is 0, and d is 0. Sealing agent for dripping method.
- 一般式(1)で表される構造を有する(メタ)アクリレート化合物は、aが2~4であることを特徴とする請求項1又は2記載の液晶滴下工法用シール剤。 3. The sealing agent for liquid crystal dropping method according to claim 1, wherein the (meth) acrylate compound having a structure represented by the general formula (1) has a of 2 to 4.
- 一般式(1)で表される構造を有する(メタ)アクリレート化合物の含有量が、硬化性樹脂成分全体の5~80重量%であることを特徴とする請求項1、2又は3記載の液晶滴下工法用シール剤。 4. The liquid crystal according to claim 1, 2 or 3, wherein the content of the (meth) acrylate compound having a structure represented by the general formula (1) is 5 to 80% by weight of the entire curable resin component. Sealing agent for dripping method.
- 更に、エポキシ基を有する硬化性樹脂及びマロン酸ジヒドラジドを含有することを特徴とする請求項1、2、3又は4記載の液晶滴下工法用シール剤。 Furthermore, the sealing agent for liquid crystal dropping methods of Claim 1, 2, 3 or 4 characterized by containing the curable resin which has an epoxy group, and malonic acid dihydrazide.
- 更に、液晶滴下工法用シール剤の全量に対して、重合禁止剤を50~2000ppm含有することを特徴とする請求項1、2、3、4又は5記載の液晶滴下工法用シール剤。 6. The sealing agent for liquid crystal dropping method according to claim 1, further comprising 50 to 2000 ppm of a polymerization inhibitor based on the total amount of the sealing agent for liquid crystal dropping method.
- 請求項1、2、3、4、5又は6記載の液晶滴下工法用シール剤と、導電性微粒子とを含有することを特徴とする上下導通材料。 A vertical conduction material comprising the sealing agent for a liquid crystal dropping method according to claim 1, 2, 3, 4, 5, or 6, and conductive fine particles.
- 請求項1、2、3、4、5又は6記載の液晶滴下工法用シール剤及び/又は請求項7記載の上下導通材料を用いてなることを特徴とする液晶表示素子。 A liquid crystal display element comprising the sealing agent for liquid crystal dropping method according to claim 1, 2, 3, 4, 5 or 6, and / or the vertical conduction material according to claim 7.
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Also Published As
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CN101978313A (en) | 2011-02-16 |
JP5584800B2 (en) | 2014-09-03 |
CN101978313B (en) | 2013-01-16 |
JP2013257567A (en) | 2013-12-26 |
KR20100138893A (en) | 2010-12-31 |
TW200949392A (en) | 2009-12-01 |
JP2013257568A (en) | 2013-12-26 |
TWI474089B (en) | 2015-02-21 |
JPWO2009119688A1 (en) | 2011-07-28 |
JP5584801B2 (en) | 2014-09-03 |
JP5508001B2 (en) | 2014-05-28 |
KR101579331B1 (en) | 2015-12-21 |
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