WO2021200220A1 - 液晶滴下工法用シール剤および液晶表示パネルの製造方法、ならびに液晶表示パネル - Google Patents
液晶滴下工法用シール剤および液晶表示パネルの製造方法、ならびに液晶表示パネル Download PDFInfo
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- WO2021200220A1 WO2021200220A1 PCT/JP2021/011090 JP2021011090W WO2021200220A1 WO 2021200220 A1 WO2021200220 A1 WO 2021200220A1 JP 2021011090 W JP2021011090 W JP 2021011090W WO 2021200220 A1 WO2021200220 A1 WO 2021200220A1
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- liquid crystal
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Classifications
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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
-
- 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
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
-
- 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
- G02F1/1303—Apparatus specially adapted to the manufacture of LCDs
Definitions
- the present invention relates to a sealant for a liquid crystal dropping method, a method for manufacturing a liquid crystal display panel, and a liquid crystal display panel.
- the liquid crystal dropping method has been widely used as a method of sealing a liquid crystal between a pair of substrates.
- a sealant is applied to form a seal pattern.
- the liquid crystal is dropped onto the substrate on which the seal pattern is formed or the substrate that is paired with the seal pattern, and the liquid crystals are bonded together in a vacuum.
- the seal pattern is cured by UV irradiation or heating, and the liquid crystal is sealed by the seal member.
- sealing agent used for the sealing agent for the liquid crystal dropping method a wide variety of compositions have been proposed as the sealing agent used for the sealing agent for the liquid crystal dropping method.
- a sealing agent or the like capable of forming a highly flexible sealing member has also been proposed (for example, Patent Documents 1 and 2).
- liquid crystal display panels have been used in various environments. For example, it is also required to use a liquid crystal display panel in a high temperature and high humidity environment.
- the conventional liquid crystal display panel has a problem that even if the adhesive strength between the substrate and the sealing member is high under a normal environment, the adhesive strength tends to decrease when exposed to high temperature and high humidity. .. Even with a highly flexible sealing member as described in Patent Document 1 and Patent Document 2 described above, it has been difficult to maintain sufficient adhesive strength with the substrate after the high temperature and high humidity test.
- the adhesive strength of the sealing member and the substrate during or after storage in a high temperature and high humidity environment does not necessarily correlate with the adhesive strength of the sealing member and the substrate under a normal environment. It became clear. That is, it has been difficult to improve the adhesive strength between the sealing member and the substrate when stored in a high-temperature and high-humidity environment or after storage by the conventional method.
- the conventional seal member may have insufficient moisture resistance in a high temperature and high humidity environment, which may cause a problem in the liquid crystal display panel.
- a sealant for a liquid crystal dropping method capable of forming a seal member having good adhesive strength with a substrate even when exposed to a high temperature and high humidity environment, a liquid crystal display panel using the sealant, and a manufacturing method thereof.
- a sealant for the liquid crystal dripping method capable of forming a sealing member having good adhesive strength with the substrate and having high moisture resistance even when exposed to a high temperature and high humidity environment, a liquid crystal display panel using the same, and a liquid crystal display panel using the same.
- the manufacturing method is also provided.
- the present invention provides the following first sealant for the liquid crystal dropping method.
- the sealing agent for the liquid crystal dropping method is made into a film having a thickness of 100 ⁇ m, irradiated with light of 3000 mJ / cm 2 , and at 120 ° C. for 1 hour. when heated to form a film, is measured by a dynamic viscoelasticity measuring apparatus, an initial Young's modulus at 120 ° C. of the film is not more than 1.0 ⁇ 10 8 Pa, and 121 ° C. the film, 100% under Rh environment is measured by a dynamic viscoelasticity measuring apparatus after storage for 24 hours, and PCT after Young's modulus at 120 ° C. of the film, the difference between the initial Young's modulus, is less 8.0 ⁇ 10 7 Pa , Sealing agent for liquid crystal dripping method.
- thermosetting agent selected from the group consisting of an imidazole-based thermosetting agent, an amine adduct-based thermosetting agent, and a polyamine-based thermosetting agent, [2] to [5].
- the sealant for the liquid crystal dropping method according to any one of.
- a sealing agent for a liquid crystal dropping method which comprises a polymerizable compound having a polymerizable functional group and a thermosetting agent, wherein the polymerizable compound contains an epoxy-based compound and is a sealing agent for the liquid crystal dropping method.
- the ratio of the number of active hydrogens derived from the thermosetting agent to the number of epoxy groups derived from the epoxy compound in the sealant for the liquid crystal dropping method is 0.25 or more, and the sealing agent for the liquid crystal dropping method. Is formed into a film having a thickness of 100 ⁇ m, irradiated with light of 3000 mJ / cm 2 , and heated at 120 ° C. for 1 hour to form a film.
- the coated particles further include a core composed of inorganic particles and a coated particle having a polymer layer covering the core, and the coated particle has a functional group containing an epoxy group and / or a carbon-carbon double bond on the surface.
- the sealant for the liquid crystal dropping method according to any one of [7] to [11].
- the sealant for a liquid crystal drop method according to [12] wherein the polymer layer contains a crosslinked polymer.
- the sealant for a liquid crystal dropping method according to [12] or [13], wherein the average particle size of the coated particles is 0.2 ⁇ m to 10 ⁇ m.
- the present invention also provides the following method for manufacturing a liquid crystal display panel.
- the step of dropping the liquid crystal in the region of the seal pattern of the one substrate or on the other substrate, and the step of superimposing the one substrate and the other substrate on the seal pattern is uncured.
- a method for manufacturing a liquid crystal display panel which comprises a step of curing the seal pattern and a step of curing the seal pattern.
- the present invention also provides the following liquid crystal display panels.
- [19] A liquid crystal display panel containing a cured product of the sealant for the liquid crystal dropping method according to any one of the above [1] to [14].
- the first sealant for the liquid crystal dropping method of the present invention can form a sealing member having good adhesive strength with the substrate even when exposed to a high temperature and high humidity environment. Therefore, it can be applied to a liquid crystal display panel used in various environments.
- the second sealant for the liquid crystal dropping method of the present invention can form a sealing member having good adhesive strength with the substrate and high moisture resistance even when exposed to a high temperature and high humidity environment. Therefore, it can be applied to a liquid crystal display panel used in various environments.
- the sealing agent for liquid crystal dripping method of the present invention (hereinafter, also simply referred to as "seal agent”) is a composition for producing a sealing member for a liquid crystal display panel, and is displayed on a liquid crystal display by the liquid crystal dripping method. It is preferably used when manufacturing a panel. However, it can also be used to manufacture a liquid crystal display panel by a liquid crystal injection method or the like.
- the sealants for the liquid crystal dropping method of the two embodiments will be described.
- the sealing member obtained from the conventional sealing agent often has a reduced adhesive strength to the substrate when exposed to a high temperature and high humidity environment. When such a decrease in adhesive strength occurs, problems such as liquid crystal leakage are likely to occur.
- the sealing member and the substrate can be bonded to each other during or after storage in a high temperature and high humidity environment. It was clarified that the adhesive strength can be improved. Specifically, it is the initial Young's modulus at 120 ° C.
- the sealant for curing the sealant at a predetermined condition film 1.0 ⁇ 10 8 Pa or less, and of the film which was stored under 100% Rh environment 24 hours 120 °C and PCT after Young's modulus at the difference between the initial Young's modulus is equal to or less than 8.0 ⁇ 10 7 Pa, even when exposed to high temperature and high humidity environment, the seal member is superior to the substrate bond It became clear that it has strength.
- the sealing member expands due to the heat, and stress is applied to the interface between the sealing member and the substrate. Further, the unreacted components (for example, epoxy groups) in the sealing member react with each other due to heat and moisture in the high temperature and high humidity environment, and the unreacted components react with the moisture in the environment to cause the sealing member. Distortion occurs inside the. Then, due to the strain, stress is likely to be generated at the interface between the seal member and the substrate, and the seal member and the substrate are easily peeled off.
- the unreacted components for example, epoxy groups
- the Young's modulus at 120 ° C. of the cured product of the sealing agent (sealing member) (initial Young's modulus) or less 1.0 ⁇ 10 8 Pa, sealing member is relatively soft ,
- the stress generated at the interface between the substrate and the sealing member can be absorbed.
- the fact that the amount of change between the Young's modulus after PCT and the initial Young's modulus after being left in a high temperature and high humidity environment is small means that the state change in the high temperature and high humidity environment is small, that is, the strain generated in the seal member is small. Represents. Therefore, the substrate and the sealing member can maintain high adhesive strength during and after storage in a high temperature and high humidity environment.
- the initial Young's modulus is measured as follows. First, the sealant is applied onto a paper pattern to a thickness of 100 ⁇ m using an applicator to form a film of 100 ⁇ m. Then, the film was placed in a container for nitrogen replacement, subjected to nitrogen purging for 5 minutes , irradiated with light of 3000 mJ / cm 2 (light calibrated by a sensor having a wavelength of 365 nm), and further heated at 120 ° C. for 1 hour to form a film. To make.
- the obtained film is cut into a length of 35 mm and a width of 10 mm, and the temperature is raised from 25 ° C. to 170 ° C. by a dynamic viscoelasticity measuring device (for example, DMA, manufactured by Seiko Instruments Inc., DMS6100) to store elastic modulus. To measure. Then, among the obtained results, the storage elastic modulus at 120 ° C. is defined as the initial Young's modulus.
- the initial Young's modulus is more preferably 1.0 ⁇ 10 6 to 1.0 ⁇ 10 8 Pa, and even more preferably 1.0 ⁇ 10 7 to 5.0 ⁇ 10 7 Pa.
- Young's modulus after PCT can be measured as follows. First, the film prepared in the same manner as above is allowed to stand at 121 ° C. in a 100% Rh environment for 24 hours. Then, the temperature is lowered to room temperature, and the temperature is raised from 25 ° C. to 170 ° C. by a dynamic viscoelasticity measuring device (for example, DMA, manufactured by Seiko Instruments Inc., DMS6100) to measure the storage elastic modulus. Then, among the obtained results, the storage elastic modulus at 120 ° C. is defined as the Young's modulus after PCT.
- the difference between the Young's modulus after PCT and the initial Young's modulus is more preferably 8.0 ⁇ 10 7 Pa or less, and further preferably 7.0 ⁇ 10 7 Pa or less.
- the composition of the sealant may be adjusted.
- the sealant of the present invention preferably contains a polymerizable compound having a polymerizable functional group, a photopolymerization initiator, a thermosetting agent, (meth) acrylic thermoplastic particles and the like.
- the sealant of the present embodiment usually contains a polymerizable compound having a polymerizable functional group.
- the polymerizable functional group refers to a functional group that is activated by light irradiation or heating, a thermosetting agent, a photopolymerization initiator, a catalyst, or the like to carry out a polymerization reaction.
- the polymerizable functional group include a (meth) acrylic group, a vinyl group, an acrylamide group, an epoxy group, an isocyanato group, a silanol group and the like.
- the description of (meth) acrylic in the present specification means methacryl, acrylic, or both, and the description of (meth) acryloyl means methacryloyl, acryloyl, or both of them.
- the polymerizable compound may be a monomer, an oligomer, or a polymer, but a monomer or an oligomer is preferable from the viewpoint of coatability of the sealant.
- the sealant of the present embodiment may contain only one kind of the above-mentioned polymerizable compound, or may contain two or more kinds of the above-mentioned polymerizable compound.
- R 1 is Represents a group (* represents a bond) selected from the group consisting of. That is, R 1 has a structure derived from bisphenol A, bisphenol E, or bisphenol F, and among these, a structure derived from bisphenol A or bisphenol F is preferable.
- R 2 and R 3 in the above general formula (1) are independently Represents a group (* represents a bond) selected from the group consisting of.
- m, n, and p each represent an integer of 1 to 30, and m, n, and p are more preferably 2 to 10.
- R 4 and R 5 in the above general formula (1) independently represent a hydrogen atom or a methyl group, respectively.
- the molecular weight (or weight average molecular weight) of the curable monomer is preferably 700 or more, more preferably 750 to 1300.
- the molecular weight (or weight average molecular weight) of the curable monomer is 700 or more, the cured product of the curable monomer becomes flexible, and the effect of absorbing the stress generated at the interface between the substrate and the sealing member becomes high.
- the molecular weight of the curable monomer can be adjusted by the number of n, m, or p in the above general formula (1), that is, the amount of the structure derived from ethylene oxide or the structure derived from propylene oxide.
- the weight average molecular weight of the curable monomer can be specified (in terms of polystyrene) by, for example, gel permeation chromatography (GPC).
- the total amount of the curable monomer is preferably 10% by mass or more and 30% by mass or less, and more preferably 10% by mass or more and 20% by mass or less with respect to the total amount of the polymerizable compound. If the amount of curable monomer is excessively large, the curable monomer may affect the display characteristics of the liquid crystal display panel. On the other hand, when the amount of the curable monomer is 30% by mass or less, the display characteristics of the liquid crystal display panel tend to be good. On the other hand, when the amount of the curable monomer is 10% by mass or more, the above-mentioned initial Young's modulus and post-PCT Young's modulus tend to fall within the above ranges.
- the polymerizable compound includes an epoxy compound, a (meth) acrylic / epoxy-containing compound, and a (meth) acrylic compound other than the curable monomer (hereinafter, simply “(meth) acrylic compound”) in addition to the curable monomer. It is also preferable to further include) and the like.
- the polymerizable compound contains these, the adhesive strength between the obtained sealing member and the substrate is likely to be good, and the display characteristics of the liquid crystal display panel are likely to be good.
- the epoxy compound may be a compound having an epoxy group (however, the compound corresponding to the (meth) acrylic epoxy compound described later is excluded).
- the number of epoxy groups contained in one molecule of the epoxy compound is preferably 2 or more. When the number of epoxy groups in the epoxy compound is 2 or more, the adhesiveness between the obtained sealing member and the substrate of the liquid crystal display panel becomes good. Further, the moisture resistance of the obtained sealing member is likely to increase.
- the epoxy compound may be liquid at room temperature or solid.
- the softening point of the epoxy compound is preferably 40 to 120 ° C. from the viewpoint of keeping the viscosity of the sealant in a desired range.
- the epoxy compound may be a monomer, an oligomer, or a polymer.
- the molecular weight (or weight average molecular weight) of the epoxy compound is usually preferably 220 to 3000, more preferably 250 to 2500, and even more preferably 300 to 2000.
- the ratio of the component having a molecular weight of 500 or more to the total amount of the epoxy compound is preferably 25% by mass or more.
- Epoxy compounds having a molecular weight of 500 or more are difficult to dissolve in liquid crystal displays when the liquid crystal display panel is manufactured. Therefore, the display characteristics of the obtained liquid crystal display panel are improved.
- the weight average molecular weight of the epoxy compound can be specified (in terms of polystyrene) by, for example, gel permeation chromatography (GPC).
- the structure of the epoxy compound is not particularly limited, and an example thereof includes an aromatic epoxy compound having an aromatic ring in the main chain.
- aromatic epoxy compounds include aromatic diols typified by bisphenol A, bisphenol S, bisphenol F, bisphenol AD, diols obtained by modifying these with ethylene glycol, propylene glycol, and alkylene glycol AD, and epichlorohydrin.
- Aromatic polyvalent glycidyl ether compound obtained by reaction; obtained by reaction of epichlorohydrin with novolak resin derived from phenol, cresol, etc. and formaldehyde, polyphenols represented by polyalkenylphenol, copolymers thereof, etc.
- novolak-type polyvalent glycidyl ether compounds include novolak-type polyvalent glycidyl ether compounds; glycidyl ether compounds of xylylenephenol resin; naphthalene-type epoxy compounds; diphenyl ether-type epoxy compounds; biphenyl-type epoxy compounds; and the like.
- the aromatic epoxy compound is a cresol novolac type epoxy compound, a phenol novolac type epoxy compound, a bisphenol A type epoxy compound, a bisphenol F type epoxy compound, a triphenol methane type epoxy compound, or a triphenol ethane type epoxy compound.
- Trisphenol type epoxy compound, diphenyl ether type epoxy compound, biphenyl type epoxy compound are preferable.
- the polymerizable compound may contain only one type of epoxy compound, or may contain two or more types of epoxy compound.
- the total amount of the epoxy compound is preferably 5 to 70% by mass, more preferably 10 to 50% by mass, based on the total amount of the polymerizable compound.
- the amount of the epoxy compound in the polymerizable compound is 5% by mass or more, the adhesive strength between the cured product of the sealant and the substrate of the liquid crystal display panel tends to increase.
- the amount of the epoxy compound is 70% by mass or less, the amount of unreacted components contained in the obtained sealing member tends to decrease. Therefore, the difference between the Young's modulus after PCT of the cured product of the sealant and the initial Young's modulus tends to be small.
- the (meth) acrylic / epoxy-containing compound means a compound having an epoxy group and a (meth) acrylic group in one molecule.
- the polymerizable compound contains the above-mentioned epoxy compound and the above-mentioned curable monomer, their compatibility may be low.
- the polymerizable compound further contains a (meth) acrylic / epoxy-containing compound, the compatibility between the epoxy compound and the curable monomer is enhanced. Furthermore, the elution of the epoxy compound into the liquid crystal display can also be suppressed by the (meth) acrylic / epoxy-containing compound.
- the number of epoxy groups and (meth) acrylic groups in one molecule of the (meth) acrylic / epoxy-containing compound is not particularly limited, but may be, for example, one or a plurality. Further, the number of epoxy groups and the number of (meth) acrylic groups may be the same or different.
- the (meth) acrylic-epoxy-containing compound include a (meth) acrylic-modified epoxy compound obtained by reacting an epoxy compound with (meth) acrylic acid in the presence of a basic catalyst.
- the epoxy compound used for preparing the (meth) acrylic-modified epoxy compound may be a bifunctional or higher-functional epoxy compound having two or more epoxy groups in the molecule, and may be bisphenol A type, bisphenol F type, or 2,2'-diallyl.
- Bisphenol type epoxy compounds such as bisphenol A type, bisphenol AD type, and hydrogenated bisphenol type; novolak type epoxy compounds such as phenol novolac type, cresol novolac type, biphenyl novolac type, and trisphenol novolac type; biphenyl type epoxy compounds; naphthalene Type epoxy compounds and the like are included.
- the (meth) acrylic-modified epoxy compound obtained by (meth) acrylic modification of a polyfunctional epoxy compound such as trifunctional or tetrafunctional has a high crosslink density when cured. Therefore, if the sealant contains such a (meth) acrylic-modified epoxy compound, it may be difficult to satisfy the above initial Young's modulus. Therefore, a (meth) acrylic-modified epoxy compound obtained by modifying a bifunctional epoxy compound with (meth) acrylic is preferable.
- the epoxy compound for preparing the (meth) acrylic-modified epoxy compound is more preferably a biphenyl type epoxy compound, a naphthalene type epoxy compound, and a bisphenol type epoxy compound, and a bisphenol type epoxy compound such as bisphenol A type and bisphenol F type is used. It is more preferable from the viewpoint of coating efficiency of the sealant.
- the epoxy compound for preparing the (meth) acrylic-modified epoxy compound may be one kind or two or more kinds. Further, the epoxy compound for preparing the (meth) acrylic-modified epoxy compound is preferably highly purified by a molecular distillation method, a washing method or the like.
- reaction between the above epoxy compound and (meth) acrylic acid can be carried out according to a conventional method.
- (meth) acrylic acid reacts with some of the epoxy groups in the epoxy compound to obtain a (meth) acrylic-modified epoxy compound having a (meth) acrylic group and an epoxy group.
- the molecular weight (weight average molecular weight) of the (meth) acrylic / epoxy-containing compound is preferably, for example, 310 to 1000, and more preferably 350 to 900.
- the weight average molecular weight of the (meth) acrylic / epoxy-containing compound can be measured (in terms of polystyrene) by, for example, gel permeation chromatography (GPC).
- GPC gel permeation chromatography
- the total amount of the (meth) acrylic / epoxy-containing compound is preferably 30 to 80% by mass, more preferably 40 to 70% by mass, based on the total amount of the polymerizable compound.
- the amount of the (meth) acrylic / epoxy-containing compound in the polymerizable compound is 40% by mass or more, the compatibility between the curable monomer and the epoxy compound tends to increase.
- the amount of the (meth) acrylic / epoxy-containing compound is 70% by mass or less, the above-mentioned initial Young's modulus and Young's modulus after PCT tend to be in a desired range.
- the (meth) acrylic compound is a compound containing one or more (meth) acrylic groups in one molecule and does not have an epoxy group (however, it corresponds to the above-mentioned curable monomer). (Excluding those).
- the (meth) acrylic compound may be a monomer, an oligomer, or a polymer.
- the number of (meth) acrylic groups contained in one molecule of the (meth) acrylic compound is preferably 2 or more.
- the photocurability of the sealant becomes good.
- examples of the (meth) acrylic compound include di (meth) acrylates such as polyethylene glycol, propylene glycol, and polypropylene glycol; di (meth) acrylates of tris (2-hydroxyethyl) isocyanurate; and 1 mol of neopentyl glycol.
- the glass transition temperature of the (meth) acrylic compound is preferably 25 ° C. or higher and 200 ° C. or lower from the viewpoint that the initial Young's modulus of the cured product of the sealant easily falls within a desired range.
- the glass transition temperature is more preferably 40 ° C. to 200 ° C., further preferably 50 to 150 ° C.
- the glass transition temperature is measured by a viscoelasticity measuring device (DMS).
- the molecular weight (or weight average molecular weight) of the (meth) acrylic compound is preferably 310 to 1000, more preferably 400 to 900.
- the weight average molecular weight of the (meth) acrylic compound can be measured (in terms of polystyrene) by, for example, gel permeation chromatography (GPC).
- GPC gel permeation chromatography
- the amount of the (meth) acrylic compound is preferably 5 to 70% by mass, more preferably 10 to 50% by mass, based on the total amount of the polymerizable compound.
- the amount of the (meth) acrylic compound is 5% by mass or more, the photocurability of the sealant tends to be good.
- the amount of the (meth) acrylic compound is 70% by mass or less, the moisture resistance of the obtained sealing member tends to be good.
- the total amount of the polymerizable compound (total amount of the above-mentioned curable monomer, epoxy compound, (meth) acrylic / epoxy-containing compound, (meth) acrylic compound, etc.) is 60 to 80% by mass with respect to the total amount of the sealant. Is preferable, and 65 to 75% by mass is more preferable.
- the polymerizable compound is contained in the sealant in the above range, the curability of the sealant becomes good, and a seal member having high strength can be obtained.
- the sealant preferably contains a photopolymerization initiator.
- the photopolymerization initiator may be a self-cleaving type photopolymerization initiator or a hydrogen abstraction type photopolymerization initiator as long as it is a compound capable of generating an active species by irradiation with light. ..
- the sealing agent may contain only one kind of photopolymerization initiator, or may contain two or more kinds of photopolymerization initiators.
- Examples of self-cleaving photopolymerization initiators include benzyl dimethyl ketal such as alkylphenone compounds (for example, 2,2-dimethoxy-1,2-diphenylethane-1-one (IRGACURE 651 manufactured by BASF)), 2-. ⁇ -Aminoalkylphenone such as methyl-2-morpholino (4-thiomethylphenyl) propan-1-one (IRGACURE 907 manufactured by BASF), 1-hydroxy-cyclohexyl-phenyl-ketone (IRGACURE 184 manufactured by BASF), etc.
- alkylphenone compounds for example, 2,2-dimethoxy-1,2-diphenylethane-1-one (IRGACURE 651 manufactured by BASF)
- 2-. ⁇ -Aminoalkylphenone such as methyl-2-morpholino (4-thiomethylphenyl) propan-1-one (IRGACURE 907 manufactured by BASF), 1-hydroxy-cyclohexyl-phenyl-ketone (IR
- ⁇ -Hydroxyalkylphenone etc.
- Acylphosphine oxide compounds eg 2,4,6-trimethylbenzoindiphenylphosphine oxide, etc.
- Titanocene compounds eg, bis ( ⁇ 5-2,4-cyclopentadiene-1-yl))- Bis (2,6-difluoro-3- (1H-pyrrole-1-yl) -phenyl) titanium, etc.
- Acetphenone compounds eg, diethoxyacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1- On, benzyl dimethyl ketal, 1- (4-isopropylphenyl) -2-hydroxy-2-methylpropan-1-one, 4- (2-hydroxyethoxy) phenyl- (2-hydroxy-2-propyl) ketone, 1, -Hydroxycyclohexyl-phenylketone, 2-methyl-2-morpholino (4-thiomethylphenyl) propan-1-one, 2-
- hydrogen abstraction-type photopolymerization initiators examples include benzophenone compounds (eg, benzophenone, o-benzoylmethylbenzoate methyl-4-phenylbenzophenone, 4,4'-dichlorobenzophenone, hydroxybenzophenone, 4-benzoyl-4'-.
- benzophenone compounds eg, benzophenone, o-benzoylmethylbenzoate methyl-4-phenylbenzophenone, 4,4'-dichlorobenzophenone, hydroxybenzophenone, 4-benzoyl-4'-.
- Methyl-diphenylsulfide acrylicized benzophenone, 3,3', 4,4'-tetra (t-butylperoxycarbonyl) benzophenone, 3,3'-dimethyl-4-methoxybenzophenone, etc.
- thioxanthone compounds eg, thioxanthone, 2-Chlorothioxanthone, 1-chloro-4-propoxythioxanthone, 1-chloro-4-ethoxythioxanthone (Lambson Limited Co., Ltd. Speedcure CPTX), 2-isopropylxantone (Lambson Limited Co., Ltd.
- the absorption wavelength of the photopolymerization initiator is not particularly limited, and for example, a photopolymerization initiator that absorbs light having a wavelength of 360 nm or more is preferable. Among them, it is more preferable to absorb light in the visible light region, a photopolymerization initiator that absorbs light having a wavelength of 360 to 780 nm is more preferable, and a photopolymerization initiator that absorbs light having a wavelength of 360 to 430 nm is particularly preferable.
- Examples of the photopolymerization initiator that absorbs light having a wavelength of 360 nm or more include an alkylphenone-based compound, an acylphosphine oxide-based compound, a titanosen-based compound, an oxime ester-based compound, a thioxanthone-based compound, and an anthraquinone-based compound, and are preferable. It is an alkylphenone-based compound or an oxime ester-based compound.
- the structure of the photopolymerization initiator can be specified by combining high performance liquid chromatography (HPLC) and liquid chromatography mass spectrometry (LC / MS) with NMR measurement or IR measurement.
- HPLC high performance liquid chromatography
- LC / MS liquid chromatography mass spectrometry
- the molecular weight of the photopolymerization initiator is preferably 200 or more and 5000 or less, for example.
- the molecular weight of the photopolymerization initiator is 200 or more, it is difficult for the photopolymerization initiator to elute into the liquid crystal display when the sealant and the liquid crystal display come into contact with each other.
- the molecular weight is 5000 or less, the compatibility with the above-mentioned (meth) acrylic compound and the like is enhanced, and the curability of the sealant tends to be improved.
- the molecular weight of the photopolymerization initiator is more preferably 230 or more and 3000 or less, and further preferably 230 or more and 1500 or less.
- the molecular weight of the photopolymerization initiator can be determined as the "relative molecular weight" of the molecular structure of the main peak detected when analyzed by high performance liquid chromatography (HPLC: High Performance Liquid Chromatography).
- the main peak refers to the peak with the highest intensity (the peak with the highest peak height) among all the peaks detected at the detection wavelength characteristic of each compound (for example, 400 nm in the case of a thioxanthone compound).
- the relative molecular weight corresponding to the peak peak of the detected main peak can be measured by liquid chromatography-mass spectrometry (LC / MS: Liquid Chromatography Mass Spectrometry).
- the amount of the photopolymerization initiator is preferably 0.1 to 15% by mass, more preferably 0.5 to 10% by mass, still more preferably 1 to 10% by mass, based on the total amount of the sealant.
- the amount of the photopolymerization initiator is 0.1% by mass or more, the photocurability of the sealant tends to be good.
- the amount of the photopolymerization initiator is 15% by mass or less, it becomes difficult for the photopolymerization initiator to elute into the liquid crystal display.
- the sealing agent preferably contains a thermosetting agent.
- the thermosetting agent may be any component capable of curing the above-mentioned polymerizable compound, particularly an epoxy compound or a (meth) acrylic / epoxy-containing compound by heating.
- thermosetting agents do not cure the above-mentioned epoxy compounds and (meth) acrylic / epoxy-containing compounds under normal storage conditions (room temperature, visible light, etc.), but compounds that cure these compounds by heating. Is preferable.
- the sealing agent containing such a thermosetting agent both storage stability and thermosetting property can be achieved at the same time.
- thermosetting agent has a solubility in water at 20 ° C. of preferably 5 g / 100 g or less, more preferably 3 g / 100 g or less, and further preferably 1 g / 100 g or less.
- solubility of the thermosetting agent in water is within this range, it becomes difficult for the thermosetting agent to elute into the liquid crystal together with water in the atmosphere.
- thermosetting agent a compound capable of curing an epoxy compound (hereinafter, also referred to as “epoxy curing agent”) is preferable.
- the melting point of the epoxy curing agent is preferably 50 ° C. or higher and 250 ° C. or lower, more preferably 100 ° C. or higher and 200 ° C. or lower, and 150 ° C. or higher, from the viewpoint of increasing the viscosity stability of the sealing agent and not impairing the moisture resistance of the obtained sealing member. It is more preferably ° C. or higher and 200 ° C. or lower.
- the sealing agent can be made one-component curable.
- workability is excellent because it is not necessary to mix the main agent and the curing agent at the time of use.
- epoxy curing agents include organic acid dihydrazide-based thermal latent curing agents, imidazole-based thermal latent curing agents, dicyandiamide-based thermal latent curing agents, amine adduct-based thermal latent curing agents, and polyamine-based thermal latent curing agents. Contains agents.
- organic acid dihydrazide-based thermal latent curing agents include adipic acid dihydrazide (melting point 181 ° C.), 1,3-bis (hydrazinocarboethyl) -5-isopropylhydranthin (melting point 120 ° C.), 7,11-octa. Includes decadien-1,18-dicarbohydrazide (melting point 160 ° C.), dodecanedioic acid dihydrazide (melting point 190 ° C.), sebacic acid dihydrazide (melting point 189 ° C.) and the like.
- imidazole-based thermal latent curing agents examples include 2,4-diamino-6- [2'-ethylimidazolyl- (1')]-ethyltriazine (melting point 215-225 ° C.) and 2-phenylimidazole (melting point). 137 to 147 ° C.) and the like.
- dicyandiamide-based thermal latent curing agents examples include dicyandiamide (melting point 209 ° C.) and the like.
- the amine adduct-based thermal latent curing agent is a thermal latent curing agent composed of an additional compound obtained by reacting an amine-based compound having catalytic activity with an arbitrary compound.
- amine adduct-based thermal latent curing agents are Ajinomoto Fine-Techno's Amicure PN-40 (melting point 110 ° C), Ajinomoto Fine-Techno's Amicure PN-23 (melting point 100 ° C), and Ajinomoto Fine-Techno's Amicure PN.
- the polyamine-based thermal latent curing agent is a thermal latent curing agent having a polymer structure obtained by reacting amine and epoxy, and an example thereof is ADEKA Hardener EH4339S (softening point 120 to 130 ° C.) manufactured by ADEKA Corporation. , And ADEKA Hardener EH4357S (softening point 73 to 83 ° C.) and the like.
- an imidazole-based thermal latent curing agent, an amine adduct-based thermal latent curing agent, or a polyamine-based thermal latent curing agent is preferable from the viewpoint of availability, compatibility with other components, and the like.
- the sealant may contain only one type of epoxy curing agent, or may contain two or more types of sealant.
- the content of the thermosetting agent is preferably 1 to 20% by mass, more preferably 2 to 18% by mass, still more preferably 3 to 15% by mass, based on the total amount of the sealing agent.
- the amount of the thermosetting agent is in the above range, the thermosetting property of the sealing agent becomes good.
- the sealant further contains (meth) acrylic thermoplastic polymer particles (hereinafter, also simply referred to as “polymer particles”).
- the average particle size of the polymer particles is preferably 0.05 to 5 ⁇ m, preferably 0.07 to 3 ⁇ m, from the viewpoint of ensuring good dispersibility in the sealant.
- the average particle size is a value measured by the Coulter counter method.
- the softening point temperature of the polymer particles is preferably 50 to 120 ° C, more preferably 60 to 80 ° C.
- the (meth) acrylic thermoplastic polymer melts and becomes compatible with other components in the sealant.
- the compatible (meth) acrylic thermoplastic polymer swells and suppresses the decrease in viscosity of the sealant before curing. As a result, it becomes difficult for the components in the sealant to elute into the liquid crystal display.
- the polymer particles may be polymer particles containing a structural unit derived from a (meth) acrylic acid ester monomer, but may be polymer particles obtained by copolymerizing a (meth) acrylic acid ester monomer with another monomer. It is preferable to have.
- the amount of the (meth) acrylic acid ester-derived structural unit in the polymer particles is preferably 50 to 99.9% by mass, more preferably 60 to 80% by mass.
- the amount of the structural unit derived from other monomers in the polymer particles is preferably 0.1 to 50% by mass, more preferably 20 to 40% by mass.
- Examples of (meth) acrylic acid ester monomers include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, and amyl (meth) acrylate.
- Monofunctional (meth) acrylic acid esters such as hexadecyl (meth) acrylate, octadecyl (meth) acrylate, butoxyethyl (meth) acrylate, phenoxyethyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, and glycidyl (meth) acrylate.
- the polymer particles may contain only one type of structure derived from these, or may contain two or more types of structures.
- examples of other monomers include acrylamides; acid monomers such as (meth) acrylic acid, itaconic acid, and maleic acid; aromatic vinyl compounds such as styrene and styrene derivatives; 1,3-butadiene, 1,3-. Conjugated dienes such as pentadiene, isoprene, 1,3-hexadiene and chloroprene; polyfunctional monomers such as divinylbenzene and diacrylates; and the like are included.
- the polymer particles may contain only one type of structure derived from another polymer, or may contain two or more types of structures.
- the polymer particles may be either a non-crosslinked type or a crosslinked type, and may be a composite type having a core-shell structure composed of a crosslinked core and a non-crosslinked shell layer. Whether the polymer particles are non-crosslinked or crosslinked can be adjusted by the type of other monomer.
- the content of the polymer particles is preferably 3% by mass or more, more preferably 5 to 30% by mass, based on the total amount of the sealant. When the amount of the polymer particles is in the above range, the moisture resistance of the obtained sealing member becomes good.
- the sealant may further contain inorganic particles.
- the sealing agent contains inorganic particles, the viscosity of the sealing agent, the strength of the obtained sealing member, the linear expansion property, and the like tend to be improved.
- inorganic particle materials include calcium carbonate, magnesium carbonate, barium sulfate, magnesium sulfate, aluminum silicate, zirconium silicate, iron oxide, titanium oxide, titanium nitride, aluminum oxide (alumina), zinc oxide, silicon dioxide, and titanic acid. Includes potassium, kaolin, talc, glass beads, sericite-activated clay, bentonite, aluminum oxide, silicon nitride and the like.
- the sealing agent may contain only one kind of inorganic particles, or may contain two or more kinds of sealing agents. Among the above, silicon dioxide or talc is preferable as the inorganic particles.
- the shape of the inorganic particles may be a fixed shape such as a spherical shape, a plate shape, a needle shape, or a non-fixed shape.
- the average primary particle size of the inorganic particles is preferably 1.5 ⁇ m or less, and the specific surface area is more preferably 0.5 to 20 m 2 / g.
- the average primary particle size of the inorganic particles can be measured by the laser diffraction method described in JIS Z8825-1.
- the specific surface area of the inorganic particles can be measured by the BET method described in JIS Z8830.
- the content of the inorganic particles is preferably 0.1 to 25% by mass, more preferably 3 to 20% by mass, still more preferably 5 to 18% by mass, based on the total amount of the sealant.
- the content of the inorganic particles is 0.1% by mass or more, the moisture resistance of the obtained sealing member tends to increase, and when it is 25% by mass or less, the coating stability of the sealing agent is not easily impaired.
- Organic Particle Sealing Agent may further contain organic particles in addition to the above (meth) acrylic thermoplastic polymer particles or inorganic particles. When the sealant contains organic particles, it becomes easy to adjust the elastic modulus of the sealant after photocuring.
- organic particles examples include silicone particles, styrene particles such as a styrene / divinylbenzene copolymer, and polyolefin particles.
- the sealing agent may contain only one kind of organic particles, or may contain two or more kinds of organic particles.
- the average primary particle size of the organic particles is preferably 0.05 to 13 ⁇ m, more preferably 0.1 to 10 ⁇ m, and even more preferably 0.1 to 8 ⁇ m.
- the shape of the organic particles is not particularly limited, but is preferably spherical, and more preferably true spherical.
- the average primary particle size of organic particles can be measured by microscopy, specifically image analysis with an electron microscope.
- it is preferable that the surface of the organic particles is smooth. A smooth surface reduces the specific surface area and increases the amount of organic particles that can be added to the sealant.
- the content of the organic particles is preferably 0.1 to 20% by mass, more preferably 1 to 15% by mass, still more preferably 3 to 12% by mass, based on the total amount of the sealant.
- the amount of organic particles is in this range, the Young's modulus of the sealant after photocuring tends to fall within a desired range.
- the sealant of the present embodiment is a thermal radical polymerization initiator, a coupling agent such as a silane coupling agent, an ion trapping agent, an ion exchanger, a leveling agent, a pigment, a dye, and a sensitizer, if necessary.
- a coupling agent such as a silane coupling agent, an ion trapping agent, an ion exchanger, a leveling agent, a pigment, a dye, and a sensitizer, if necessary.
- Plasticizers, antifoaming agents and the like may be further included.
- silane coupling agents examples include vinyltrimethoxysilane, ⁇ - (meth) acryloxipropyltrimethoxysilane, ⁇ -glycidoxypropyltrimethoxysilane, ⁇ -glycidoxypropyltriethoxysilane, and the like.
- the amount of the silane coupling agent is preferably 0.01 to 6% by mass, more preferably 0.1 to 5% by mass, still more preferably 0.5 to 3% by mass, based on the total amount of the sealing agent.
- the content of the silane coupling agent is 0.01% by mass or more, the obtained sealing member tends to have sufficient adhesiveness.
- the sealant may further contain a spacer or the like for adjusting the gap of the liquid crystal display panel.
- the total amount of other components is preferably 1 to 50% by mass with respect to the total amount of the sealant.
- the viscosity of the sealant is unlikely to increase excessively, and the coating stability of the sealant is unlikely to be impaired.
- the viscosity of the E-type viscometer of the sealing agent at 25 ° C. and 2.5 rpm is preferably 200 to 450 Pa ⁇ s, more preferably 250 to 400 Pa ⁇ s.
- the viscosity is in the above range, when a pair of substrates are superposed on each other via a sealant (seal pattern), the sealant is likely to be deformed so as to fill these gaps. Therefore, the gap between the pair of substrates of the liquid crystal display panel can be appropriately controlled.
- the thixotropy index (TI value) of the sealant is preferably 1.0 to 1.5, more preferably 1.1 to 1.3, from the viewpoint of the coatability of the sealant.
- the TI value is determined by using an E-type viscometer, the viscosity of the sealant at room temperature (25 ° C.) and 0.5 rpm is ⁇ 1, and the viscosity of the sealant at 5 rpm is ⁇ 2. It is a value obtained by applying to.
- TI value (viscosity ⁇ 1 (25 ° C) at 0.5 rpm) / (viscosity ⁇ 2 (25 ° C) at 5 rpm) ... (1)
- Second Sealing Agent for Liquid Crystal Dropping Method As described above, the sealing member obtained from the conventional sealing agent often has a reduced adhesive strength to the substrate when exposed to a high temperature and high humidity environment. When such a decrease in adhesive strength occurs, problems such as liquid crystal leakage are likely to occur.
- the conventional sealing member may not have sufficient moisture resistance, and the liquid crystal display panel is likely to be affected when exposed to a high temperature and high humidity environment.
- the adhesive strength between the seal member and the substrate can be improved during or after storage in a high temperature and high humidity environment.
- it is the initial Young's modulus at 120 ° C. for curing the sealant at a predetermined condition film 1.0 ⁇ 10 8 Pa or less, and of the film which was stored under 100% Rh environment 24 hours 120 °C and PCT after Young's modulus at the difference between the initial Young's modulus is equal to or less than 8.0 ⁇ 10 7 Pa, even when exposed to high temperature and high humidity environment, the seal member is superior to substrate adhesion It became clear that it has strength.
- the reason and the method for measuring Young's modulus are as described in the section of the first sealant.
- the initial Young's modulus is more preferably 1.0 ⁇ 10 6 to 1.0 ⁇ 10 8 Pa, further preferably 1.0 ⁇ 10 7 to 5.0 ⁇ 10 7 Pa.
- the difference between the post-PCT Young's modulus and the initial Young's modulus is more preferably 8.0 ⁇ 10 7 Pa or less, and even more preferably 7.0 ⁇ 10 7 Pa or less.
- the ratio of the number of active hydrogens derived from the thermosetting agent in the sealant to the number of epoxy groups derived from the epoxy compound in the sealant (the number of the active hydrogens / the number of the epoxy groups). Is 0.25 or more. Therefore, the moisture resistance of the obtained sealing member becomes very good. The reason is that the amount of active hydrogen is relatively large relative to the number of epoxy groups. With such a ratio, unreacted epoxy groups are less likely to remain after curing, and the crosslink density in the sealing member is increased. Therefore, it becomes difficult for the sealing member to absorb or permeate moisture.
- the number of epoxy groups derived from the epoxy compound is obtained by dividing the amount (mass) of the epoxy compound in the sealant by the epoxy equivalent of the compound.
- the epoxy equivalent is a value obtained by dividing the molecular weight (or weight average molecular weight) of the epoxy compound by the number of epoxy groups contained in one molecule of the epoxy compound (molecular weight of the epoxy compound / number of epoxy groups). ..
- the amount of active hydrogen derived from the thermosetting agent is a value obtained by dividing the amount (mass) of the thermosetting agent in the sealing agent by the active hydrogen equivalent of the thermosetting agent.
- the active hydrogen equivalent is the value obtained by dividing the molecular weight (or weight average molecular weight) of the heat curing agent by the number of active hydrogens bonded to the nitrogen atom contained in one molecule of the heat curing agent (molecular weight of the heat curing agent / number of active hydrogens). Is.
- the sealant contains a plurality of epoxy compounds
- the number of epoxy groups is calculated for each epoxy compound, and the total value of these is taken as the total number of epoxy groups in the sealant.
- the number of active hydrogens is calculated for each thermosetting agent, and the total value of these is taken as the number of active hydrogens in the entire sealant.
- the above ratio (the number of active hydrogens / the number of epoxy groups) is more preferably 0.25 to 1.0, and even more preferably 0.3 to 0.6.
- the composition of the sealant may be adjusted.
- the components constituting the sealant will be described in detail.
- the sealant of the present embodiment contains a polymerizable compound having a polymerizable functional group.
- the polymerizable compound may be a monomer, an oligomer, or a polymer, but is usually a monomer or an oligomer. Further, the sealant of the present embodiment may contain only one kind of the above-mentioned polymerizable compound, or may contain two or more kinds of the above-mentioned polymerizable compound.
- the sealant of the present embodiment contains at least an epoxy compound as a polymerizable compound.
- the epoxy compound in the present specification is a polymerizable compound having an epoxy group, and the coating particles described later are not included in the epoxy compound.
- the sealant of the present embodiment also contains the curable monomer represented by the above-mentioned general formula (1).
- epoxy compounds include compounds having an epoxy group and no (meth) acrylic group (hereinafter, also referred to as “epoxy compound”), and compounds having an epoxy group and a (meth) acrylic group (hereinafter,). , Also referred to as “(meth) acrylic epoxy compound”).
- the epoxy compound may be a compound having an epoxy group (however, the compound corresponding to the (meth) acrylic epoxy compound described later is excluded).
- the number of epoxy groups contained in one molecule of the epoxy compound is preferably 2 or more. When the number of epoxy groups in the epoxy compound is 2 or more, the adhesiveness between the obtained sealing member and the substrate of the liquid crystal display panel becomes good. Further, the moisture resistance of the obtained sealing member is likely to increase.
- the epoxy compound may be liquid at room temperature or solid.
- the softening point of the epoxy compound is preferably 40 to 110 ° C. from the viewpoint of the viscosity of the obtained sealant.
- the epoxy equivalent of the epoxy compound is preferably 200 to 2000, more preferably 300 to 1000. When the epoxy equivalent is in this range, it becomes easy to satisfy the ratio of the active hydrogen equivalent of the thermosetting agent to the epoxy equivalent of the above-mentioned epoxy compound.
- the epoxy compound may be a monomer, an oligomer, or a polymer.
- the molecular weight (or weight average molecular weight) of the epoxy compound is usually preferably 220 to 3000, more preferably 250 to 2500, and even more preferably 300 to 2000.
- the ratio of the component having a molecular weight of 500 or more to the total amount of the epoxy compound is preferably 25% by mass or more.
- Epoxy compounds having a molecular weight of 500 or more are difficult to dissolve in liquid crystal displays when the liquid crystal display panel is manufactured. Therefore, the display characteristics of the obtained liquid crystal display panel are improved.
- the weight average molecular weight of the epoxy compound can be specified (in terms of polystyrene) by, for example, gel permeation chromatography (GPC).
- the structure of the epoxy compound is not particularly limited, and an example thereof includes an aromatic epoxy compound having an aromatic ring in the main chain.
- the structure of the epoxy compound is the same as that of the epoxy compound contained in the first sealant described above.
- the sealant may contain only one type of epoxy compound, or may contain two or more types of sealant.
- the total amount of the epoxy compound is preferably 5 to 70% by mass, more preferably 10 to 50% by mass, based on the total amount of the polymerizable compound.
- the amount of the epoxy compound in the polymerizable compound is 5% by mass or more, the adhesive strength between the cured product of the sealant and the substrate of the liquid crystal display panel tends to increase.
- the amount of the epoxy compound is 70% by mass or less, the amount of unreacted components contained in the obtained sealing member tends to decrease. Therefore, the difference between the Young's modulus after PCT of the cured product of the sealant and the initial Young's modulus tends to be small.
- the (meth) acrylic / epoxy-containing compound means a compound having an epoxy group and a (meth) acrylic group in one molecule.
- the polymerizable compound contains the above-mentioned epoxy compound and the below-mentioned curable monomer, their compatibility may be low.
- the polymerizable compound further contains a (meth) acrylic / epoxy-containing compound, the compatibility between the epoxy compound and the curable monomer is enhanced. Furthermore, the elution of the epoxy compound into the liquid crystal display can also be suppressed by the (meth) acrylic / epoxy-containing compound.
- the specific structure and preferable structure of the (meth) acrylic / epoxy-containing compound are the same as those of the (meth) acrylic / epoxy compound contained in the first sealant described above.
- the molecular weight (weight average molecular weight) of the (meth) acrylic / epoxy-containing compound is preferably, for example, 310 to 1000, and more preferably 350 to 900.
- the weight average molecular weight of the (meth) acrylic / epoxy-containing compound can be measured (in terms of polystyrene) by, for example, gel permeation chromatography (GPC).
- GPC gel permeation chromatography
- the total amount of the (meth) acrylic / epoxy-containing compound is preferably 30 to 80% by mass, more preferably 40 to 70% by mass, based on the total amount of the polymerizable compound.
- the amount of the (meth) acrylic / epoxy-containing compound is 30% by mass or more, the compatibility between the curable monomer and the epoxy compound tends to increase.
- the amount of the (meth) acrylic / epoxy-containing compound is 80% by mass or less, the above-mentioned initial Young's modulus and Young's modulus after PCT tend to be in a desired range.
- the polymerizable compound further contains the curable monomer represented by the general formula (1) described in the section of the first sealant, the initial Young's modulus of the cured product of the sealant and the Young's modulus after PCT However, it tends to fall within the above range.
- the molecular weight (or weight average molecular weight) of the curable monomer represented by the above general formula (1) is preferably 700 or more, more preferably 750 to 1300.
- the molecular weight (or weight average molecular weight) of the curable monomer is 700 or more, the cured product of the curable monomer becomes flexible, and the effect of absorbing the stress generated at the interface between the substrate and the sealing member becomes high.
- the molecular weight of the curable monomer can be adjusted by the number of n, m, and p in the above general formula (1), that is, the amount of the structure derived from ethylene oxide or the structure derived from propylene oxide.
- the weight average molecular weight of the curable monomer can be specified (in terms of polystyrene) by, for example, gel permeation chromatography (GPC).
- the total amount of the curable monomer is preferably 10% by mass or more and 30% by mass or less, and more preferably 10% by mass or more and 20% by mass or less with respect to the total amount of the polymerizable compound. If the amount of curable monomer is excessively large, the curable monomer may affect the display characteristics of the liquid crystal display panel. On the other hand, when the amount of the curable monomer is 30% by mass or less, the display characteristics of the liquid crystal display panel tend to be good. On the other hand, when the amount of the curable monomer is 10% by mass or more, the above-mentioned initial Young's modulus and post-PCT Young's modulus tend to fall within the above ranges.
- the polymerizable compound preferably further contains a (meth) acrylic compound having a structure other than the curable monomer in addition to the epoxy compound and the curable monomer.
- a (meth) acrylic compound When the polymerizable compound contains a (meth) acrylic compound, the adhesive strength between the substrate and the sealing member tends to be good, and the display characteristics of the liquid crystal display panel tend to be good.
- the (meth) acrylic compound contained in the polymerizable compound of the present embodiment is a compound containing one or more (meth) acrylic groups in one molecule and does not have an epoxy group (however, as described above). Except for curable monomers).
- the (meth) acrylic compound may be a monomer, an oligomer, or a polymer.
- the number of (meth) acrylic groups contained in one molecule of the (meth) acrylic compound is preferably 2 or more.
- the photocurability of the sealant becomes good.
- the (meth) acrylic compound is the same as the (meth) acrylic compound contained in the first sealant described above.
- the glass transition temperature of the (meth) acrylic compound is preferably 25 ° C. or higher and lower than 200 ° C. from the viewpoint that the initial Young's modulus of the cured product of the sealant easily falls within a desired range.
- the glass transition temperature is more preferably 40 ° C. to 200 ° C., further preferably 50 to 150 ° C.
- the glass transition temperature is measured by a viscoelasticity measuring device (DMS).
- the molecular weight (or weight average molecular weight) of the (meth) acrylic compound is preferably 310 to 1000, more preferably 400 to 900.
- the weight average molecular weight of the (meth) acrylic compound can be measured (in terms of polystyrene) by, for example, gel permeation chromatography (GPC).
- GPC gel permeation chromatography
- the amount of the (meth) acrylic compound is preferably 5 to 70% by mass, more preferably 10 to 50% by mass, based on the total amount of the polymerizable compound.
- the amount of the (meth) acrylic compound is 5% by mass or more, the photocurability of the sealant tends to be good.
- the amount of the (meth) acrylic compound is 70% by mass or less, the moisture resistance of the obtained sealing member tends to be good.
- the total amount of the polymerizable compound (total amount of epoxy group compound, (meth) acrylic / epoxy-containing compound, curable monomer, (meth) acrylic compound, etc.) is 60 to 80% by mass based on the total amount of the sealant. Is preferable, and 65 to 75% by mass is more preferable.
- the polymerizable compound is contained in the sealant in the above range, the curability of the sealant becomes good, and a seal member having higher strength can be obtained.
- the sealing agent contains a thermosetting agent.
- the thermosetting agent is a component capable of curing the above-mentioned polymerizable compound, particularly an epoxy compound or a (meth) acrylic / epoxy-containing compound by heating, and is a sealing agent with respect to the number of epoxy groups in the above-mentioned sealing agent.
- the ratio of the number of active hydrogens derived from the thermosetting agent is not particularly limited as long as it is 0.25 or more.
- the thermosetting agent does not cure the above-mentioned epoxy compounds or (meth) acrylic / epoxy-containing compounds under normal storage conditions (room temperature, visible light, etc.), but it is a compound that cures these compounds by heating. Is preferable. According to the sealing agent containing such a thermosetting agent, both storage stability and thermosetting property can be achieved at the same time.
- the active hydrogen equivalent of the thermosetting agent is preferably 10 to 500, more preferably 100 to 300.
- the active equivalent of the thermosetting agent is in the above range, it becomes easy to satisfy the ratio of the number of active hydrogens derived from the thermosetting agent in the sealant to the number of epoxy groups in the sealant described above.
- thermosetting agent an epoxy curing agent similar to the epoxy curing agent contained in the first sealing agent described above is preferable.
- the melting point of the epoxy curing agent is preferably 50 ° C. or higher and 250 ° C. or lower, more preferably 100 ° C. or higher and 200 ° C. or lower, from the viewpoint of enhancing the viscosity stability of the sealing agent and not impairing the moisture resistance of the obtained sealing member. More preferably, it is 150 ° C. or higher and 200 ° C. or lower.
- the sealing agent can be made one-component curable. When the sealing agent is one-component curable, workability is excellent because it is not necessary to mix the main agent and the curing agent at the time of use.
- the structure of the epoxy curing agent is the same as the structure of the epoxy curing agent contained in the first sealant described above.
- an imidazole-based thermal latent curing agent, an amine adduct-based thermal latent curing agent, or a polyamine-based thermal latent curing agent is preferable from the viewpoint of availability, compatibility with other components, and the like.
- the sealant may contain only one type of epoxy curing agent, or may contain two or more types of sealant.
- the content of the thermosetting agent is preferably 1 to 20% by mass, more preferably 2 to 18% by mass, still more preferably 3 to 15% by mass, based on the total amount of the sealing agent.
- the amount of the thermosetting agent is in the above range, the thermosetting property of the sealing agent becomes good.
- the sealant preferably contains a curing catalyst.
- the curing catalyst may be any compound that functions as a catalyst when the above-mentioned polymerizable compound is polymerized or crosslinked. Examples of the curing catalyst include an imidazole-based curing catalyst, an amine adduct-based curing catalyst, a modified amine-based curing catalyst, and the like.
- imidazole-based curing catalysts examples include 2-phenyl-4,5-dihydroxymethylimidazole, 2-phenyl-4-methyl-5-hydroxymethylimidazole, 2-hydroxymethylimidazole, 1-benzyl-5-hydroxymethylimidazole. , 1,2-Dihydroxyethylimidazole, 1,3,5-triazine-2,4,6 (1H, 3H, 5H) -trione and 6- [2- (2-methyl-1H-imidazole-1-yl)) Ethyl] -1,3,5-triazine-2,4-diamine and the like are included.
- Examples of amine adduct-based curing catalysts include Amicure PN-23 (manufactured by Ajinomoto Fine-Techno Co., Ltd.) and the like.
- Examples of the modified amine-based curing catalyst include Fujicure FXR-1020, FXR-1081, FXR-1121, FXR-1032, FXR-1131 (all manufactured by Fuji Kasei Kogyo Co., Ltd.) and the like.
- the melting point of the curing catalyst is preferably 100 ° C. or higher, more preferably 140 to 300 ° C.
- the melting point of the curing catalyst is 100 ° C. or higher, the storage stability of the sealant tends to be good.
- the content of the curing catalyst is preferably 0.1 to 20% by mass, more preferably 0.2 to 15% by mass, and even more preferably 0.3 to 13% by mass with respect to the total amount of the sealant.
- the amount of the curing catalyst is in the above range, the curing of the sealant becomes good.
- the sealant preferably further contains coated particles.
- the coated particles in the present specification are particles having a core composed of inorganic particles and a polymer layer covering the core, and have a functional group containing an epoxy group and / or a carbon-carbon double bond on the surface.
- Examples of carbon-carbon double bonds include vinyl groups, allyl groups, and (meth) acrylic groups.
- the polymer layer may completely cover the core, but may only partially cover it. However, the coverage is preferably 50% or more, more preferably 80% or more.
- the number of epoxy groups per 1 g of the coated particles is preferably 1 to 300 ⁇ eq / g. From the viewpoint of storage stability, the above value is preferably 1 to 150 ⁇ eq / g. Further, from the viewpoint of improving the adhesive strength, the above value is preferably 5 to 300 ⁇ eq / g.
- the amount of epoxy group can be specified by a known measurement method.
- the number of functional groups having a carbon-carbon double bond per 1 g of the coated particles is preferably 1 to 300 ⁇ eq / g. Within this range, the storage stability of the sealant becomes good.
- the method for measuring the functional group equivalent having a carbon-carbon double bond is not particularly limited, and one example thereof is the iodine value method (14th revised Japanese Pharmacopoeia General Test Method 65. Oil and Fat Test Method).
- the average particle size of the coated particles is preferably 0.2 ⁇ m to 10 ⁇ m, more preferably 0.2 to 5 ⁇ m, and even more preferably 0.2 to 3 ⁇ m.
- the thickness of the polymer layer in the coated particles is preferably 0.001 to 1 ⁇ m, more preferably 0.001 to 0.5 ⁇ m. When the thickness of the polymer layer is within the above range, the affinity between the coated particles and the above-mentioned polymerizable compound is enhanced, not only the coatability of the sealing agent is improved, but also the deformation of the obtained sealing member can be suppressed.
- the thickness of the polymer layer can be specified from the average particle size of the core and the average particle size of the coated particles.
- the average thickness of the polymer layer (average particle size of coated particles-average particle size of core) / 2.
- the average particle size of the core and the average particle size of the coated particles can be specified by a laser method particle size measuring device using a laser having a wavelength of 632.8 nm, and are average values when the average particle size of the primary particles is measured 10 times. And.
- Examples of cores of coated particles include crystalline silica, molten silica, silica obtained by the precipitation method, silica obtained by the sol-gel method, calcium carbonate, magnesium carbonate, barium sulfate, magnesium sulfate, aluminum silicate, zirconium silicate, and zirconium dioxide.
- silica and titania silica Includes composite oxides of silica such as zirconia and other metals.
- silicas such as crystalline silica having excellent thermal stability, fused silica, and silica obtained by the sol-gel method are more preferable.
- the core may be hydrophobized.
- Examples of the hydrophobic treatment include a method of treating the core material with a hydrophobic surface treatment agent such as cyclic siloxane, silane coupling agent, titanate-based coupling agent, and hexaalkyl disilazane.
- a hydrophobic surface treatment agent such as cyclic siloxane, silane coupling agent, titanate-based coupling agent, and hexaalkyl disilazane.
- cyclic siloxane such as hexamethylcyclotrisiloxane or hexaalkyldisilazane such as hexamethyldisilazane
- the hygroscopicity of the obtained sealing member tends to be lowered.
- the polymer layer can be formed by radical polymerization of a monomer having a radically polymerizable functional group in the presence of the core.
- a monomer having a radically polymerizable functional group epoxy acrylate having a carbon-carbon double bond, a polyfunctional carbon-carbon double bond compound, etc.
- the monomer may be radically polymerized to form a polymer layer.
- a functional group on the core and a monomer having a radically polymerizable functional group are grafted by a dealcohol condensation reaction or the like. They may be bonded to form a polymer layer. Further, a compound having a carbon-carbon double bond such as an acrylic silane compound is reacted with the core, and then a monomer having a radically polymerizable functional group (epoxy acrylate having a carbon-carbon double bond or polyfunctional carbon-carbon) is reacted. A method in which a double bond compound) is further reacted to form a core layer is particularly preferable.
- a polymer obtained by polymerizing a polyfunctional carbon-carbon double bond compound is referred to as a crosslinked polymer.
- the polymer layer described above preferably contains a crosslinked polymer.
- thermosetting agent and a photopolymerization initiator are used together with an epoxy acrylate having a carbon-carbon double bond and a polyfunctional carbon-carbon double bond compound, which are monomers having a radically polymerizable functional group. May be used. These can be the same as the thermosetting agent and the photopolymerization initiator contained in the sealant. The amount thereof is also appropriately selected according to the desired polymer layer.
- Propyltrimethoxysilane and the like are included.
- Examples of the epoxy acrylate used when forming the polymer layer include glycidyl (meth) acrylate, glycidoxystyrene, glycidoxymethylstyrene, glycidoxyethylstyrene and the like.
- the polyfunctional carbon-carbon double bond compound used when forming the polymer layer is a compound having two or more carbon-carbon double bonds, and examples thereof include divinylbenzene and divinylbiphenyl.
- Aromatic vinyl-based monomers such as polyfunctional aromatic vinyl compounds such as trivinylbenzene and divinylnaphthalene; ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, triethylene glycol di (meth).
- a monomer other than epoxy acrylate or a polyfunctional carbon-carbon double bond compound may be used in combination.
- examples of other monomers include aromatic vinyl-based monomers such as styrene, vinyltoluene, 2,4-dimethylstyrene, p-tert-butylstyrene, vinylnaphthalene; methyl (meth) acrylate, (meth) acrylic.
- the content of the coating particles is preferably 0.1 to 30% by mass, more preferably 3 to 20% by mass, still more preferably 5 to 20% by mass, based on the total amount of the sealant. When the amount of the coating particles is in the above range, the moisture resistance of the sealant becomes good.
- the sealant preferably contains a photopolymerization initiator.
- the photopolymerization initiator may be a self-cleaving type photopolymerization initiator or a hydrogen abstraction type photopolymerization initiator as long as it is a compound capable of generating an active species by irradiation with light. ..
- the sealing agent may contain only one kind of photopolymerization initiator, or may contain two or more kinds of photopolymerization initiators.
- photopolymerization initiator contained in the sealant of the present embodiment are the same as those of the photopolymerization initiator contained in the first sealant described above.
- the absorption wavelength of the photopolymerization initiator is not particularly limited, and for example, a photopolymerization initiator that absorbs light having a wavelength of 360 nm or more is preferable. Among them, it is more preferable to absorb light in the visible light region, a photopolymerization initiator that absorbs light having a wavelength of 360 to 780 nm is more preferable, and a photopolymerization initiator that absorbs light having a wavelength of 360 to 430 nm is particularly preferable.
- Examples of the photopolymerization initiator that absorbs light having a wavelength of 360 nm or more include an alkylphenone-based compound, an acylphosphine oxide-based compound, a titanosen-based compound, an oxime ester-based compound, a thioxanthone-based compound, and an anthraquinone-based compound, and are preferable. It is an alkylphenone-based compound or an oxime ester-based compound.
- the structure of the photopolymerization initiator can be specified by the above method.
- the molecular weight of the photopolymerization initiator is preferably 200 or more and 5000 or less, for example.
- the molecular weight of the photopolymerization initiator is 200 or more, it is difficult for the photopolymerization initiator to elute into the liquid crystal display when the sealant and the liquid crystal display come into contact with each other.
- the molecular weight is 5000 or less, the compatibility with the above-mentioned (meth) acrylic compound and the like is enhanced, and the curability of the sealant tends to be improved.
- the molecular weight of the photopolymerization initiator is more preferably 230 or more and 3000 or less, and further preferably 230 or more and 1500 or less.
- the molecular weight of the photopolymerization initiator can be determined by the method described above.
- the amount of the photopolymerization initiator is preferably 0.1 to 15% by mass, more preferably 0.5 to 10% by mass, still more preferably 1 to 10% by mass, based on the total amount of the sealant.
- the amount of the photopolymerization initiator is 0.1% by mass or more, the photocurability of the sealant tends to be good.
- the amount of the photopolymerization initiator is 15% by mass or less, it becomes difficult for the photopolymerization initiator to elute into the liquid crystal display.
- the organic particle sealant may further contain organic particles, if necessary. When the sealant contains organic particles, it becomes easy to adjust the Young's modulus of the sealant and the like.
- organic particles examples include silicone particles, acrylic particles, styrene particles such as a styrene / divinylbenzene copolymer, and polyolefin particles.
- the sealing agent may contain only one kind of organic particles, or may contain two or more kinds of organic particles.
- the average primary particle size of the organic particles is preferably 0.05 to 13 ⁇ m, more preferably 0.1 to 10 ⁇ m, and even more preferably 0.1 to 8 ⁇ m.
- the shape of the organic particles is not particularly limited, but is preferably spherical, and more preferably true spherical.
- the average primary particle size of the organic particles can be specified by the method described above.
- the content of the organic particles is preferably 0.1 to 20% by mass, more preferably 1 to 15% by mass, still more preferably 3 to 13% by mass, based on the total amount of the sealant.
- the amount of organic particles is in the above range, the elastic modulus of the sealant after photocuring tends to be within a desired range.
- the sealant may further contain inorganic particles.
- the sealing agent contains inorganic particles, the viscosity of the sealing agent, the strength of the obtained sealing member, the linear expansion property, and the like tend to be improved.
- the content of the inorganic particles is preferably 0.1 to 25% by mass, more preferably 3 to 20% by mass, still more preferably 5 to 18% by mass, based on the total amount of the sealant.
- the content of the inorganic particles is 0.1% by mass or more, the moisture resistance of the obtained sealing member tends to increase, and when it is 25% by mass or less, the coating stability of the sealing agent is not easily impaired.
- the sealant of the present embodiment is a thermal radical polymerization initiator, a coupling agent such as a silane coupling agent, an ion trapping agent, an ion exchanger, a leveling agent, a pigment, a dye, and a sensitizer, if necessary.
- a coupling agent such as a silane coupling agent, an ion trapping agent, an ion exchanger, a leveling agent, a pigment, a dye, and a sensitizer, if necessary.
- Plasticizers, antifoaming agents and the like may be further included.
- silane coupling agents examples include vinyltrimethoxysilane, ⁇ - (meth) acryloxipropyltrimethoxysilane, ⁇ -glycidoxypropyltrimethoxysilane, ⁇ -glycidoxypropyltriethoxysilane, and the like.
- the amount of the silane coupling agent is preferably 0.01 to 6% by mass, more preferably 0.1 to 5% by mass, still more preferably 0.5 to 3% by mass, based on the total amount of the sealing agent.
- the content of the silane coupling agent is 0.01% by mass or more, the obtained sealing member tends to have sufficient adhesiveness.
- the sealant may further contain a spacer or the like for adjusting the gap of the liquid crystal display panel.
- the total amount of other components is preferably 1 to 50% by mass with respect to the total amount of the sealant.
- the viscosity of the sealant is unlikely to increase excessively, and the coating stability of the sealant is unlikely to be impaired.
- the viscosity of the E-type viscometer of the sealing agent at 25 ° C. and 2.5 rpm is preferably 200 to 450 Pa ⁇ s, more preferably 250 to 400 Pa ⁇ s.
- the viscosity is in the above range, when a pair of substrates are superposed on each other via a sealant (seal pattern), the sealant is likely to be deformed so as to fill these gaps. Therefore, the gap between the pair of substrates of the liquid crystal display panel can be appropriately controlled.
- the thixotropy index (TI value) of the sealant is preferably 1.0 to 1.5, more preferably 1.1 to 1.3, from the viewpoint of the coatability of the sealant.
- the TI value is determined by using an E-type viscometer, the viscosity of the sealant at room temperature (25 ° C.) and 0.5 rpm is ⁇ 1, and the viscosity of the sealant at 5 rpm is ⁇ 2. It is a value obtained by applying to.
- TI value (viscosity ⁇ 1 (25 ° C) at 0.5 rpm) / (viscosity ⁇ 2 (25 ° C) at 5 rpm) ... (1)
- the liquid crystal display panel of the present invention includes a pair of substrates, a frame-shaped seal member arranged between the substrates, and a liquid crystal filled between the pair of substrates and inside the frame-shaped seal member.
- the sealing member is a cured product of the above-mentioned sealing agent.
- the sealing member obtained from the above-mentioned first sealing agent or the second sealing agent has high adhesive strength with the substrate, and even if the sealing member is thinned, liquid crystal leakage or the like is unlikely to occur. Further, the sealing agent is less likely to contaminate the liquid crystal display. Therefore, afterimages and the like are unlikely to occur when the liquid crystal display panel is used.
- the pair of substrates are both transparent substrates.
- transparent substrate materials include glass or polycarbonate, polyethylene terephthalate, polyether sulfone, PMMA and the like.
- a matrix-shaped TFT, a color filter, a black matrix, etc. are arranged on the surface of the display board or the facing board.
- An alignment film is further formed on the surface of the display substrate or the facing substrate.
- the alignment film includes known organic alignment agents, inorganic alignment agents, and the like. Further, a known liquid crystal can be used as the liquid crystal.
- the liquid crystal display panel manufacturing method generally includes a liquid crystal dropping method and a liquid crystal injection method, but the liquid crystal display panel manufacturing method of the present invention is preferably the liquid crystal dropping method.
- the method for manufacturing a liquid crystal display panel by the liquid crystal dropping method is as follows: 1) a seal pattern forming step of applying the above-mentioned sealant to one substrate to form a frame-shaped seal pattern, and 2) a state in which the seal pattern is uncured. Then, the liquid crystal is dropped on one substrate and in the region surrounded by the seal pattern, or on the other substrate and in the region surrounded by the seal pattern when the other substrate and one substrate are opposed to each other. It includes a step, 3) a superposition step of superimposing one substrate and the other substrate via a seal pattern, and 4) a curing step of curing the seal pattern.
- the above-mentioned sealant is applied to one of the substrates.
- the method of applying the sealant is not particularly limited, and is not particularly limited as long as it is a method capable of forming a seal pattern with a desired thickness and width, such as screen printing or application with a dispenser, and a known method of applying the sealant. Is similar to.
- the shape of the seal pattern to be formed may be appropriately selected according to the application of the liquid crystal display panel, etc., and may be a shape in which the liquid crystal does not leak. For example, it may have a rectangular frame shape, but is not limited to the shape.
- the line width of the seal pattern is preferably 0.2 to 1.0 mm, more preferably 0.2 to 0.5 mm.
- the pair of substrates are opposed to each other with the seal pattern uncured.
- the state in which the seal pattern is uncured means a state in which the curing reaction of the sealant has not progressed to the gel point.
- the seal pattern may be semi-cured by irradiating or heating the seal pattern in order to suppress the dissolution of the sealant in the liquid crystal.
- the method of dropping the liquid crystal is the same as the known method of dropping the liquid crystal, and the liquid crystal may be dropped on the substrate on which the seal pattern is formed, and the liquid crystal may be dropped on the substrate on which the seal pattern is not formed (the other substrate). May be dropped.
- one substrate and the other substrate are overlapped so as to face each other via a seal pattern. At this time, the gap between the substrates is controlled to be within a desired range.
- the seal pattern is cured.
- the method for curing the seal pattern is not particularly limited, but it is preferable that the seal pattern is temporarily cured by irradiation with light having a predetermined wavelength and then finally cured by heating. By light irradiation, the seal pattern can be instantly cured, and the components in the sealant can be suppressed from being dissolved in the liquid crystal display.
- the wavelength of the light to be irradiated is appropriately selected according to the type of the photopolymerization initiator, and light containing visible light is preferable.
- the light irradiation time is, for example, about 10 minutes, although it depends on the composition of the sealant.
- the amount of energy to be irradiated at this time may be an amount of energy sufficient to cure the (meth) acrylic compound or the (meth) acrylic / epoxy-containing compound.
- the epoxy compound or the (meth) acrylic / epoxy-containing compound may be cured by heating.
- the heating temperature depends on the composition of the sealant, but is, for example, 100 to 150 ° C., and the heating time is preferably about 2 hours.
- Epoxy compound 1 JER, Epicoat 1004, softening point 97 ° C., epoxy equivalent: 900, weight average molecular weight: 1650
- Epoxy compound 2 ADEKA, EP-4003S, epoxy equivalent: 470, weight average molecular weight: 940
- Acrylic modified epoxy compound manufactured by KSM, BAEM-50, epoxy equivalent: about 470 (estimated)
- Thermosetting agent Thermosetting agent 1 ADEKA, EH-4357S, polyamine type, melting point 75 to 85 ° C, solubility in water: insoluble, amino group equivalent: 0.013
- Thermosetting agent 2 Made by Japan Finechem Company, Inc., dihydrazide malonic acid (MDH), melting point 150-160 ° C., solubility in water: 10 g / 100 g, amino group equivalent: 0.045
- Photopolymerization initiator 1 BASF, Irgacure 651
- Photopolymerization Initiator 2 Omnipol-TX, manufactured by IGM Regins
- Epoxy compound 2 100 parts by mass, acrylic modified epoxy compound 495 parts by mass, acrylic compound 60 parts by mass, curable monomer (A-1) prepared in Synthesis Example 1 80 parts by mass, heat curing agent 30 parts by mass, inorganic particles 120 parts by mass Parts, 100 parts by mass of acrylic thermoplastic polymer particles, 10 parts by mass of silane coupling agent, and 10 parts by mass of photopolymerization initiator are sufficiently mixed using three rolls so as to form a uniform liquid, and the liquid crystal is dropped. A sealant for the construction method was obtained.
- Examples 1-2 to 1-10 and Comparative Examples 1-1 to 1-5 A sealant for the liquid crystal dropping method was obtained in the same manner as in Example 1-1, except that the type and amount of each component were changed as shown in Table 1.
- the obtained sealant for the liquid crystal dropping method was applied on a paper pattern to a thickness of 100 ⁇ m using an applicator. Then, the film was placed in a container for nitrogen replacement, subjected to nitrogen purging for 5 minutes , irradiated with light of 3000 mJ / cm 2 (light calibrated by a sensor having a wavelength of 365 nm), and further heated at 120 ° C. for 1 hour to form a film. Made.
- the Young's modulus of the obtained film was 25 ° C to 170 ° C by cutting the obtained cured film with scissors having a length of 35 mm and a width of 10 mm and using a dynamic viscoelasticity measuring device (DMA, manufactured by Seiko Instruments Inc., DMS6100). It was measured by raising the temperature to. Then, among the obtained results, the value of the storage elastic modulus at 120 ° C. was defined as the initial Young's modulus.
- DMA dynamic viscoelasticity measuring device
- the film prepared in the same manner as above was placed in a PCT testing machine (PC-422R8D manufactured by Hirayama Seisakusho Co., Ltd.) and exposed to a environment of 121 ° C. and 100% Rh for 24 hours. Then, after the temperature was lowered to room temperature, the film was taken out and measured using a dynamic viscoelasticity measuring device in the same manner as described above. Then, among the obtained results, the value of the storage elastic modulus at 120 ° C. was defined as the Young's modulus after PCT.
- a 38 mm ⁇ 38 mm quadrangle (frame shape) was applied onto a PIN (manufactured by EHC) to form a seal pattern (cross-sectional area 2500 ⁇ m 2).
- the paired glass substrates were bonded under reduced pressure so as to be perpendicular to the glass substrate on which the seal pattern was formed, and then the glass substrates were opened to the atmosphere and bonded.
- the two laminated glass substrates are held in a light-shielding box for 1 minute , then irradiated with light containing visible light of 3000 mJ / cm 2 (light having a wavelength of 370 to 450 nm), and further heated at 120 ° C. for 1 hour. The seal was cured.
- the bonded glass substrate was placed in a PCT testing machine (PC-422R8D manufactured by Hirayama Seisakusho Co., Ltd.), exposed to a temperature of 121 ° C. and 100% Rh for 24 hours, and then taken out after the temperature dropped to room temperature for testing. I got a piece.
- PCT testing machine PC-422R8D manufactured by Hirayama Seisakusho Co., Ltd.
- the portion 4.5 mm from the outer circumference of the seal pattern of the obtained test piece was vertically pressed at a speed of 5 mm / min using an indentation tester (Model 210 manufactured by Intesco), and the stress when the seal was peeled off was measured. ..
- the adhesive strength was determined by dividing the stress by the seal line width drawn with the liquid crystal sealant. Then, it was evaluated according to the following criteria. ⁇ : Peeling at 25 N / mm or more ⁇ : Peeling at 15 N / mm or more and less than 25 N / mm ⁇ : Peeling at less than 15 N / mm
- the above-mentioned sealant for the liquid crystal dripping method was used with a dispenser (Musashi Engineering Co., Ltd., Shotmaster) to form a transparent electrode and an alignment film in advance on a 40 mm x 45 mm glass substrate (EHC Co., Ltd., RT-).
- a 35 mm ⁇ 35 mm quadrangular (frame-shaped) seal pattern (cross-sectional area 3500 ⁇ m 2 ) was formed on the DM88-PIN) as a main seal, and a 38 mm ⁇ 38 mm quadrangular (frame-shaped) seal pattern was formed on the outer periphery thereof.
- a liquid crystal material (MLC-6609-000 manufactured by Merck & Co., Inc.) corresponding to the capacity of the panel after bonding was precisely dropped into the frame of the main seal using a dispenser.
- the paired glass substrates were bonded under reduced pressure, and then opened to the atmosphere for bonding.
- the main seal is masked with a substrate coated with a 36 mm ⁇ 36 mm square black matrix, and visible light of 500 mJ / cm 2 is emitted.
- the main seal was cured by irradiating the contained light (light having a wavelength of 370 to 450 nm) and further heating at 120 ° C. for 1 hour.
- a polarizing film was attached to both sides of the obtained liquid crystal cell to obtain a liquid crystal display panel.
- the evaluation was performed as follows.
- ⁇ When the liquid crystal is oriented up to the main seal of the liquid crystal display panel and there is no color unevenness ⁇ : When color unevenness occurs in the vicinity of the main seal over a range of less than 1 mm ⁇ : 1 mm from the vicinity of the main seal When color unevenness occurs over the above range
- the difference is, when it exceeds 8.0 ⁇ 10 7 Pa (Comparative Example with the case (Comparative Example 1-3), or PCT after Young's modulus and the initial Young's modulus of the initial Young's modulus of more than 1.0 ⁇ 10 8 1-1, 1-2, 1-4, and 1-5) all had low adhesive strength after PCT.
- the curable monomer represented by the above general formula (1) was not contained, the display characteristics were also low (Comparative Examples 1-2, 1-3).
- the coated particles had an epoxy group on the surface.
- the thickness of the polymer layer of the coated particles was 0.009 ⁇ m.
- Epoxy compound 1 JER, Epicoat 1004, softening point 97 ° C., epoxy equivalent: 900, weight average molecular weight: 1650
- Epoxy compound 2 ADEKA, EP-4003S, epoxy equivalent: 470, weight average molecular weight: 940
- Acrylic modified epoxy compound manufactured by KSM, BAEM-50, epoxy equivalent: about 470 (estimated)
- Admatex SO-C1
- Epoxy compound 2 80 parts by mass, acrylic modified epoxy compound 510 parts by mass, acrylic compound 60 parts by mass, curable monomer (A-1) prepared in Synthesis Example 1 80 parts by mass, heat curing agent 30 parts by mass, inorganic particles 120 parts by mass Parts, 100 parts by mass of organic particles, 10 parts by mass of silane coupling agent, and 10 parts by mass of photopolymerization initiator are sufficiently mixed using three rolls so as to form a uniform liquid to prepare a sealant for the liquid crystal dropping method. Obtained.
- Example 2-2 to 2-14 and Comparative Examples 2-1 to 2-5 A sealant for the liquid crystal dropping method was obtained in the same manner as in Example 2-1 except that the type and amount of each component were changed as shown in Table 2 or 3.
- the obtained sealant for the liquid crystal dropping method was applied on a paper pattern to a thickness of 100 ⁇ m using an applicator. Then, the film was placed in a container for nitrogen replacement, subjected to nitrogen purging for 5 minutes , irradiated with light of 3000 mJ / cm 2 (light calibrated by a sensor having a wavelength of 365 nm), and further heated at 120 ° C. for 1 hour to form a film. Made.
- the Young's modulus of the obtained film was 25 ° C to 170 ° C by cutting the obtained cured film with scissors having a length of 35 mm and a width of 10 mm and using a dynamic viscoelasticity measuring device (DMA, manufactured by Seiko Instruments Inc., DMS6100). It was measured by raising the temperature to. Then, among the obtained results, the value of the storage elastic modulus at 120 ° C. was defined as the initial Young's modulus.
- DMA dynamic viscoelasticity measuring device
- the film prepared in the same manner as above was placed in a PCT testing machine (PC-422R8D manufactured by Hirayama Seisakusho Co., Ltd.) and exposed to a environment of 121 ° C. and 100% Rh for 24 hours. Then, after the temperature was lowered to room temperature, the film was taken out and measured using a dynamic viscoelasticity measuring device in the same manner as described above. Then, among the obtained results, the value of the storage elastic modulus at 120 ° C. was defined as the Young's modulus after PCT.
- the two laminated glass substrates are held in a light-shielding box for 1 minute , then irradiated with light containing visible light of 3000 mJ / cm 2 (light having a wavelength of 370 to 450 nm), and further heated at 120 ° C. for 1 hour. The seal was cured.
- the bonded glass substrate was placed in a PCT testing machine (PC-422R8D manufactured by Hirayama Seisakusho Co., Ltd.), exposed to a temperature of 121 ° C. and 100% Rh for 24 hours, and then taken out after the temperature dropped to room temperature for testing. I got a piece.
- PCT testing machine PC-422R8D manufactured by Hirayama Seisakusho Co., Ltd.
- the portion 4.5 mm from the outer circumference of the seal pattern of the obtained test piece was vertically pressed at a speed of 5 mm / min using an indentation tester (Model 210 manufactured by Intesco), and the stress when the seal was peeled off was measured. ..
- the adhesive strength was determined by dividing the stress by the seal line width drawn with the liquid crystal sealant. Then, it was evaluated according to the following criteria. ⁇ : Peeling at 25 N / mm or more ⁇ : Peeling at 15 N / mm or more and less than 25 N / mm ⁇ : Peeling at less than 15 N / mm
- Viscosity increase rate B / A x 100 ⁇ : Viscosity increase rate is 120% or less ⁇ : Viscosity increase rate is more than 120%
- Examples 2-11 and 2-14 the adhesive strength was particularly high and the amount of moisture permeation was also low. Further, even when coated particles were contained, the adhesive strength was improved and the amount of moisture permeation was reduced (Examples 2-12 to 2-14).
- the cured product of the sealant of the present invention has high adhesive strength with the substrate even after being stored in a high temperature and high humidity environment. Therefore, the sealant is very useful as a sealant or the like for producing a seal member for various liquid crystal display panels.
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Abstract
Description
[1]液晶滴下工法に使用する、液晶滴下工法用シール剤であって、前記液晶滴下工法用シール剤を厚み100μmの膜状にし、3000mJ/cm2の光を照射し、120℃で1時間加熱してフィルムを形成したとき、動的粘弾性測定装置で測定される、前記フィルムの120℃における初期ヤング率が1.0×108Pa以下であり、かつ前記フィルムを121℃、100%Rh環境下で24時間保存後に動的粘弾性測定装置で測定される、前記フィルムの120℃におけるPCT後ヤング率と、前記初期ヤング率との差が、8.0×107Pa以下である、液晶滴下工法用シール剤。
R2およびR3は、それぞれ独立に、
[4]前記重合性化合物の総量に対する前記硬化性モノマーの総量が、10質量%以上30質量%以下である、[2]または[3]に記載の液晶滴下工法用シール剤。
[5](メタ)アクリル系熱可塑性ポリマー粒子をさらに含み、前記(メタ)アクリル系熱可塑性ポリマー粒子の量が、10質量%以上である、[2]~[4]のいずれかに記載の液晶滴下工法用シール剤。
[7]重合性官能基を有する重合性化合物と、熱硬化剤と、を含む液晶滴下工法用シール剤であって、前記重合性化合物がエポキシ基系化合物を含み、前記液晶滴下工法用シール剤中の前記エポキシ系化合物由来のエポキシ基の数に対する、前記液晶滴下工法用シール剤中の前記熱硬化剤由来の活性水素の数の比率が0.25以上であり、前記液晶滴下工法用シール剤を厚み100μmの膜状にし、3000mJ/cm2の光を照射し、120℃で1時間加熱してフィルムを形成したとき、動的粘弾性測定装置で測定される、前記フィルムの120℃における初期ヤング率が1.0×108Pa以下であり、かつ前記フィルムを121℃、100%Rh環境下で24時間保存後に動的粘弾性測定装置で測定される、前記フィルムの120℃におけるPCT後ヤング率と、前記初期ヤング率との差が、8.0×107Pa以下である、液晶滴下工法用シール剤。
[10]前記重合性化合物の総量に対する前記硬化性モノマーの総量が、10質量%以上30質量%以下である、[8]または[9]に記載の液晶滴下工法用シール剤。
[11]硬化触媒をさらに含み、前記硬化触媒の融点が100℃以上である、[7]~[10]のいずれかに記載の液晶滴下工法用シール剤。
[13]前記ポリマー層が、架橋型ポリマーを含む、[12]に記載の液晶滴下工法用シール剤。
[14]前記被覆粒子の平均粒子径が0.2μm~10μmである、[12]または[13]に記載の液晶滴下工法用シール剤。
[15]一対の基板の一方の基板上に、[1]~[14]のいずれかに記載の液晶滴下工法用シール剤を塗布し、シールパターンを形成する工程と、前記シールパターンが未硬化の状態において、前記一方の基板の前記シールパターンの領域内、または他方の基板上に液晶を滴下する工程と、前記一方の基板と前記他方の基板とを、前記シールパターンを介して重ね合わせる工程と、前記シールパターンを硬化させる工程と、を含む、液晶表示パネルの製造方法。
[17]前記光が、可視光を含む、[16]に記載の液晶表示パネルの製造方法。
[19]上記[1]~[14]のいずれかに記載の液晶滴下工法用シール剤の硬化物を含む、液晶表示パネル。
本発明の液晶滴下工法用シール剤(以下、単に「シール剤」とも称する)は、液晶表示パネルのシール部材を作製するための組成物であり、液晶滴下工法で液晶表示パネルを作製する場合に好適に用いられる。ただし、液晶注入工法等で液晶表示パネルを作製するためにも用いることができる。以下、2つの実施形態の液晶滴下工法用シール剤について説明する。
上述のように、従来のシール剤から得られるシール部材は、高温高湿環境に晒されると、基板に対する接着強度が低下することが多かった。そして、このような接着強度低下が生じると、液晶漏れ等の不具合が生じやすかった。
本実施形態のシール剤は通常、重合性官能基を有する重合性化合物を含む。本明細書において、重合性官能基とは、光照射または加熱、熱硬化剤や光重合開始剤、触媒等によって活性化されて、重合反応をする官能基をいう。当該重合性官能基の例には、(メタ)アクリル基、ビニル基、アクリルアミド基、エポキシ基、イソシアナート基、シラノール基等が含まれる。なお、本明細書における(メタ)アクリルとの記載は、メタクリル、アクリル、またはこれらの両方を表し、(メタ)アクリロイルとの記載は、メタクリロイル、アクリロイル、またはこれらの両方を表す。
シール剤は、光重合開始剤を含むことが好ましい。光重合開始剤は、光の照射によって、活性種を発生可能な化合物であればよく、自己開裂型の光重合開始剤であってもよく、水素引き抜き型の光重合開始剤であってもよい。シール剤は、光重合開始剤を一種のみ含んでいてもよく、二種以上含んでいてもよい。
シール剤は、熱硬化剤を含むことも好ましい。熱硬化剤は、加熱により上記重合性化合物、特にエポキシ化合物や(メタ)アクリル・エポキシ含有化合物を硬化させることが可能な成分であればよい。ただし、熱硬化剤は、通常の保存条件下(室温、可視光線下等)では、上述のエポキシ化合物や、(メタ)アクリル・エポキシ含有化合物を硬化させないが、加熱によってこれらの化合物を硬化させる化合物であることが好ましい。このような熱硬化剤を含有するシール剤によれば、保存安定性と熱硬化性とを両立できる。
また、シール剤は、(メタ)アクリル系熱可塑性ポリマー粒子(以下、単に「ポリマー粒子」とも称する)をさらに含むことが好ましい。シール剤中での良好な分散性を確保する点から、ポリマー粒子の平均粒子径は0.05~5μmが好ましく、0.07~3μmが好ましい。当該平均粒子径は、コールターカウンター法で測定される値である。
シール剤は、無機粒子をさらに含んでいてもよい。シール剤が無機粒子を含むと、シール剤の粘度や得られるシール部材の強度、および線膨張性等が良好になりやすい。
シール剤は、上記(メタ)アクリル系熱可塑性ポリマー粒子または無機粒子以外に、さらに有機粒子を含んでいてもよい。シール剤が有機粒子を含むと、シール剤の光硬化後の弾性率等を調整しやすくなる。
本実施形態のシール剤は、必要に応じて熱ラジカル重合開始剤、シランカップリング剤等のカップリング剤、イオントラップ剤、イオン交換剤、レベリング剤、顔料、染料、増感剤、可塑剤及び消泡剤等の添加剤をさらに含んでいてもよい。
シール剤のE型粘度計の25℃、2.5rpmにおける粘度は、200~450Pa・sが好ましく、250~400Pa・sがより好ましい。粘度が上記範囲にあると、シール剤(シールパターン)を介して、一対の基板を重ね合わせたときに、シール剤がこれらの隙間を埋めるように変形しやすい。そのため、液晶表示パネルの一対の基板間のギャップを適正に制御できる。
TI値=(0.5rpmにおける粘度η1(25℃))/(5rpmにおける粘度η2(25℃))・・・(1)
上述のように、従来のシール剤から得られるシール部材は、高温高湿環境に晒されると、基板に対する接着強度が低下することが多かった。そして、このような接着強度低下が生じると、液晶漏れ等の不具合が生じやすかった。従来のシール部材は耐湿性が十分でないことがあり、高温高湿環境に晒された際やその後、液晶表示パネルに影響が出やすかった。
本実施形態のシール剤は、重合性官能基を有する重合性化合物を含む。重合性化合物は、モノマーであってもよくオリゴマーであってもよく、ポリマーであってもよいが、通常モノマーまたはオリゴマーである。また、本実施形態のシール剤は、上記重合性化合物を一種のみ含んでいてもよく、二種以上含んでいてもよい。
シール剤は、熱硬化剤を含む。熱硬化剤は、加熱により上記重合性化合物、特にエポキシ化合物や(メタ)アクリル・エポキシ含有化合物を硬化させることが可能な成分であり、かつ上述のシール剤中のエポキシ基の数に対する、シール剤中の熱硬化剤由来の活性水素の数の比率が0.25以上となるものであれば特に制限されない。なお、熱硬化剤は、通常の保存条件下(室温、可視光線下等)では、上述のエポキシ化合物や、(メタ)アクリル・エポキシ含有化合物を硬化させないが、加熱によってこれらの化合物を硬化させる化合物であることが好ましい。このような熱硬化剤を含有するシール剤によれば、保存安定性と熱硬化性とを両立できる。
また、シール剤は、硬化触媒を含むことが好ましい。硬化触媒は、上述の重合性化合物が重合したり架橋したりする際に、触媒として機能する化合物であればよい。硬化触媒の例には、イミダゾール系硬化触媒、アミンアダクト系硬化触媒、変性アミン系硬化触媒等が含まれる。
シール剤は、被覆粒子をさらに含むことが好ましい。本明細書における被覆粒子は、無機粒子からなるコアと、当該コアを覆うポリマー層とを有する粒子であって、表面に、エポキシ基および/または炭素-炭素二重結合を含む官能基を有する粒子をいう。炭素-炭素二重結合の例には、ビニル基、アリル基、(メタ)アクリル基が含まれる。
シール剤は、光重合開始剤を含むことが好ましい。光重合開始剤は、光の照射によって、活性種を発生可能な化合物であればよく、自己開裂型の光重合開始剤であってもよく、水素引き抜き型の光重合開始剤であってもよい。シール剤は、光重合開始剤を一種のみ含んでいてもよく、二種以上含んでいてもよい。
シール剤は、必要に応じて有機粒子をさらに含んでいてもよい。シール剤が有機粒子を含むと、シール剤のヤング率等を調整しやすくなる。
シール剤は、無機粒子をさらに含んでいてもよい。シール剤が無機粒子を含むと、シール剤の粘度や得られるシール部材の強度、および線膨張性等が良好になりやすい。
本実施形態のシール剤は、必要に応じて熱ラジカル重合開始剤、シランカップリング剤等のカップリング剤、イオントラップ剤、イオン交換剤、レベリング剤、顔料、染料、増感剤、可塑剤及び消泡剤等の添加剤をさらに含んでいてもよい。
シール剤のE型粘度計の25℃、2.5rpmにおける粘度は、200~450Pa・sが好ましく、250~400Pa・sがより好ましい。粘度が上記範囲にあると、シール剤(シールパターン)を介して、一対の基板を重ね合わせたときに、シール剤がこれらの隙間を埋めるように変形しやすい。そのため、液晶表示パネルの一対の基板間のギャップを適正に制御できる。
TI値=(0.5rpmにおける粘度η1(25℃))/(5rpmにおける粘度η2(25℃))・・・(1)
本発明の液晶表示パネルは、一対の基板と、当該基板の間に配置された枠状のシール部材と、一対の基板間かつ枠状のシール部材の内部に充填された液晶と、を有する。当該液晶表示パネルでは、シール部材が、前述のシール剤の硬化物である。前述の第1のシール剤または第2のシール剤から得られるシール部材は、基板との接着強度が高く、シール部材を細線化しても液晶漏れ等が生じ難い。さらに、当該シール剤は、液晶を汚染し難い。したがって、液晶表示パネルの使用時に残像等が生じ難い。
[合成例1]硬化性モノマー(A-1)の合成
228gの液状ビスフェノールA(富士フィルム和光純薬社製)および0.74gの触媒(水酸化カリウム、富士フィルム和光純薬社製)を撹拌機付き高圧反応器(オートクレーブ)に仕込み、窒素ガスで置換した。次に、撹拌しながら高圧反応器を加熱し、内温が70℃に達したところで440gのエチレンオキサイド(東京化成工業社製)を高圧反応器に圧入し、さらに100℃まで加熱して4時間半反応させた。反応後、23℃まで冷却し、ビスフェノールA型エトキシレートを分取した。得られたビスフェノールA型エトキシレート316gと、アクリル酸(東京化成工業社製)144gとを、フラスコ内に仕込み、乾燥空気を送り込んで、105℃で還流撹拌しながら20時間反応させた。得られた化合物を、超純水にて20回洗浄し、上述の一般式(1)の構造を満たす硬化性モノマー(A-1)(エチレンオキサイド(EO)変性ビスフェノールA型アクリルモノマー(上述の一般式(1)におけるm+n+p=10))を得た。平均分子量を表1に示す。
228gの液状ビスフェノールA(富士フィルム和光純薬社製)および0.74gの触媒(水酸化カリウム、富士フィルム和光純薬社製)を撹拌機付き高圧反応器(オートクレーブ)に仕込み、窒素ガスで置換した。次に、撹拌しながら高圧反応器を加熱し、内温が70℃に達したところで704gのエチレンオキサイド(東京化成工業社製)を高圧反応器に圧入し、さらに100℃まで加熱して4時間半反応させた。反応後、23℃まで冷却し、ビスフェノールA型エトキシレートを分取した。得られたビスフェノールA型エトキシレート316gと、アクリル酸(東京化成工業社製)144gとをフラスコ内に仕込み、乾燥空気を送り込んで、105℃で還流撹拌しながら20時間反応させた。得られた化合物を、超純水にて20回洗浄し、上述の一般式(1)の構造を満たす硬化性モノマー(A-2)(エチレンオキサイド(EO)変性ビスフェノールA型アクリルモノマー(上述の一般式(1)におけるm+n+p=16))を得た。平均分子量を表1に示す。
228gの液状ビスフェノールA(富士フィルム和光純薬社製)および0.74gの触媒(水酸化カリウム、富士フィルム和光純薬社製)を撹拌機付き高圧反応器(オートクレーブ)に仕込み、窒素ガスで置換した。次に、撹拌しながら高圧反応器を加熱し、内温が70℃に達したところで440gのエチレンオキサイド(東京化成工業社製)を高圧反応器に圧入し、さらに100℃まで加熱して4時間半反応させた。反応後、23℃まで冷却し、ビスフェノールA型エトキシレートを分取した。得られたビスフェノールA型エトキシレート316gと、メタクリル酸(東京化成工業社製)200gとをフラスコ内に仕込み、乾燥空気を送り込んで、105℃で還流撹拌しながら20時間反応させた。得られた化合物を、超純水にて20回洗浄し、上述の一般式(1)の構造を満たす硬化性モノマー(A-3)(エチレンオキサイド(EO)変性ビスフェノールA型メタクリルモノマー(上述の一般式(1)におけるm+n+p=10))を得た。平均分子量を表1に示す。
200gの液状ビスフェノールF(富士フィルム和光純薬社製)、0.74gの触媒(水酸化カリウム、富士フィルム和光純薬社製)を撹拌機付き高圧反応器(オートクレーブ)に仕込み、窒素ガスで置換した。次に、撹拌しながら高圧反応器を加熱し、内温が70℃に達したところで440gのエチレンオキサイド(東京化成工業社製)を高圧反応器に圧入し、さらに100℃まで加熱して4時間半反応させた。反応後、23℃まで冷却し、ビスフェノールFエトキシレートを分取した。得られたビスフェノールF型エトキシレート288gと、アクリル酸(東京化成工業社製)144gとをフラスコ内に仕込み、乾燥空気を送り込んで、105℃で還流撹拌しながら20時間反応させた。得られた化合物を、超純水にて20回洗浄し、上述の一般式(1)の構造を満たす硬化性モノマー(A-4)(EO変性ビスフェノールF型アクリルモノマー(上述の一般式(1)におけるm+n+p=10))を得た。重量平均分子量を表1に示す。
200gの液状ビスフェノールF(富士フィルム和光純薬社製)、0.74gの触媒(水酸化カリウム、富士フィルム和光純薬社製)を撹拌機付き高圧反応器(オートクレーブ)に仕込み、窒素ガスで置換した。次に、撹拌しながら高圧反応器を加熱し、内温が70℃に達したところで440gのエチレンオキサイド(東京化成工業社製)を高圧反応器に圧入し、さらに100℃まで加熱して4時間半反応させた。反応後、23℃まで冷却し、ビスフェノールFエトキシレートを分取した。得られたビスフェノールF型エトキシレート288gと、メタクリル酸(東京化成工業社製)200gとを、フラスコ内に仕込み、乾燥空気を送り込んで、105℃で還流撹拌しながら20時間反応させた。得られた化合物を、超純水にて20回洗浄し、上述の一般式(1)の構造を満たす硬化性モノマー(A-5)(EO変性ビスフェノールF型メタクリルモノマー(上述の一般式(1)におけるm+n+p=10))を得た。重量平均分子量を表1に示す。
456gの液状ビスフェノールA(富士フィルム和光純薬社製)、0.74gの触媒(水酸化カリウム、富士フィルム和光純薬社製)を撹拌機付き高圧反応器(オートクレーブ)に仕込み、窒素ガスで置換した。次に、撹拌しながら高圧反応器を加熱し、内温が70℃に達したところで352gのエチレンオキサイド(東京化成工業社製)を高圧反応器に圧入し、さらに100℃まで加熱して4時間半反応させた。反応後、23℃まで冷却し、ビスフェノールA型エトキシレートを分取した。得られたビスフェノールA型エトキシレート316gと、アクリル酸(東京化成工業社製)144gとをフラスコ内に仕込み、乾燥空気を送り込んで、105℃で還流撹拌しながら20時間反応させた。得られた化合物を、超純水にて20回洗浄し、上述の一般式(1)の構造を満たす硬化性モノマー(A-6)(EO変性ビスフェノールA型アクリルモノマー(上述の一般式(1)におけるm+n+p=4))を得た。重量平均分子量を表1に示す。
上記硬化性モノマー以外の成分は、以下の化合物を用いた。
エポキシ化合物1:JER社製、エピコート1004、軟化点97℃、エポキシ当量:900、重量平均分子量:1650
エポキシ化合物2:ADEKA社製、EP-4003S、エポキシ当量:470、重量平均分子量:940
アクリル変性エポキシ化合物:ケーエスエム社製、BAEM-50、エポキシ当量:470程度(推定)
アクリル化合物:ダイセル・オルネクス社製、EBECRYL3700、重量平均分子量:500
ポリブタジエン末端ジアクリレート:大阪有機化学工業社製、BAC-45、重量平均分子量:10000
熱硬化剤1:ADEKA社製、EH-4357S、ポリアミン型、融点75~85℃、水への溶解度:不溶、アミノ基当量:0.013
熱硬化剤2:日本ファインケム社製、マロン酸ジヒドラジド(MDH)、融点150~160℃、水への溶解度:10g/100g、アミノ基当量:0.045
光重合開始剤1:BASF社製、Irgacure651
光重合開始剤2:IGM Regins社製、Omnipol-TX
アドマテックス社製、SO-C1(シリカ粒子)
アイカ工業社製微粒子ポリマー、F351
信越化学工業社製、KBM-403
エポキシ化合物2 100質量部、アクリル変性エポキシ化合物 495質量部、アクリル化合物 60質量部、合成例1で調製した硬化性モノマー(A-1) 80質量部、熱硬化剤 30質量部、無機粒子 120質量部、アクリル系熱可塑性ポリマー粒子 100質量部、シランカップリング剤 10質量部、光重合開始剤1 10質量部を、三本ロールを用いて均一な液になるように十分混合して、液晶滴下工法用シール剤を得た。
各成分の種類や量を表1に示すように変更した以外は、実施例1-1と同様に液晶滴下工法用シール剤を得た。
実施例1-1~1-10および比較例1-1~1-5で得られた液晶滴下工法用シール剤について、ヤング率、PCT後接着強度および表示特性を以下の方法で評価した。
得られた液晶滴下工法用シール剤を、離型紙のうえにアプリケーターを用いて100μmの厚みで塗布した。その後、窒素置換用の容器に入れて窒素パージを5分実施した後、3000mJ/cm2(波長365nmセンサーで校正した光)の光を照射し、さらに120℃で1時間加熱して、フィルムを作製した。
上述の液晶滴下工法用シール剤を、ディスペンサー(武蔵エンジニアリング社製、ショットマスター)を用いて、透明電極と配向膜が予め形成された40mm×45mmガラス基板(RT-DM88-PIN、EHC社製)上に、38mm×38mmの四角形(枠状)に塗布し、シールパターン(断面積2500μm2)を形成した。次いで、シールパターンを形成したガラス基板に対して垂直になるように、対になるガラス基板を減圧下で貼り合せた後、大気開放して貼り合わせた。そして、貼り合わせた2枚のガラス基板を1分間遮光ボックス内で保持した後、3000mJ/cm2の可視光を含む光(波長370~450nmの光)を照射し、さらに120℃で1時間加熱してシールを硬化させた。
◎:25N/mm以上で剥離
〇:15N/mm以上、25N/mm未満で剥離
×:15N/mm未満で剥離
上述の液晶滴下工法用シール剤を、ディスペンサー(武蔵エンジニアリング社製、ショットマスター)を用いて、透明電極と配向膜が予め形成された40mm×45mmガラス基板(EHC社製、RT-DM88-PIN)上に、メインシールとして35mm×35mmの四角形(枠状)のシールパターン(断面積3500μm2)と、その外周に38mm×38mmの四角形(枠状)のシールパターンとを形成した。
△:メインシール際の近傍に1mm未満の範囲にわたり色ムラが発生している場合
×:メインシール際近傍から1mm以上の範囲にわたり色ムラが発生している場合
[合成例1~6]硬化性モノマー(A-1)~(A-6)の合成
上述の第1の実施形態の硬化性モノマー(A-1)~(A-6)の合成方法と同様に、各硬化性モノマーを調製した。表2および表3には、平均分子量を示す。
テフロン(登録商標)製撹拌翼を有する攪拌機付きの1Lテフロン(登録商標)製三つ口フラスコにゾルゲルシリカを100g仕込み、高速攪拌しながら、グリシジルアクリレート0.28g、ジビニルベンゼン0.026g、およびパーブチルO(日本油脂社製)0.04gを混合した溶液を二流体ノズルにて噴霧した。噴霧終了後にさらに2時間撹拌した。その後、攪拌しながらフラスコを1時間かけて100℃まで昇温し、100℃で4時間保持した。
上記硬化性モノマーおよび被覆粒子以外の成分は、以下の化合物を用いた。
エポキシ化合物1:JER社製、エピコート1004、軟化点97℃、エポキシ当量:900、重量平均分子量:1650
エポキシ化合物2:ADEKA社製、EP-4003S、エポキシ当量:470、重量平均分子量:940
アクリル変性エポキシ化合物:ケーエスエム社製、BAEM-50、エポキシ当量:470程度(推定)
アクリル化合物:ダイセル・オルネクス社製、EBECRYL3700、重量平均分子量:500
ポリブタジエン末端ジアクリレート:大阪有機化学工業社製、BAC-45、重量平均分子量:10000
ADEKA社製、EH-4357S、ポリアミン型、融点75~85℃、水への溶解度:不溶、活性水素当量:79.75
四国化成社製、キュアゾール 2MZ-H、融点140~148℃
BASF社製、Irgacure651
IGM社製、Omnipol-TX
アドマテックス社製、SO-C1、シリカ粒子
アイカ工業社製微粒子ポリマー、F351
信越化学工業社製、KBM-403
エポキシ化合物2 80質量部、アクリル変性エポキシ化合物 510質量部、アクリル化合物 60質量部、合成例1で調製した硬化性モノマー(A-1) 80質量部、熱硬化剤 30質量部、無機粒子 120質量部、有機粒子 100質量部、シランカップリング剤 10質量部、光重合開始剤 10質量部を、三本ロールを用いて均一な液になるように十分混合して、液晶滴下工法用シール剤を得た。
各成分の種類や量を表2または3に示すように変更した以外は、実施例2-1と同様に液晶滴下工法用シール剤を得た。
実施例2-1~2-14および比較例2-1~2-5で得られた液晶滴下工法用シール剤について、ヤング率、PCT後接着強度および表示特性を以下の方法で評価した。
得られた液晶滴下工法用シール剤を、離型紙のうえにアプリケーターを用いて100μmの厚みで塗布した。その後、窒素置換用の容器に入れて窒素パージを5分実施した後、3000mJ/cm2(波長365nmセンサーで校正した光)の光を照射し、さらに120℃で1時間加熱して、フィルムを作製した。
まず、以下の式に基づき、エポキシ系化合物由来のエポキシ基の数および熱硬化剤由来の活性水素の数を算出した。
エポキシ基の数=(エポキシ化合物1の含有量/エポキシ化合物1のエポキシ当量)+(エポキシ化合物2の含有量/エポキシ化合物2のエポキシ当量)+(アクリル変性エポキシ化合物の含有量/当該化合物のエポキシ当量)
活性水素の数=熱硬化剤の含有量/熱硬化剤の活性水素当量
そして、上記活性水素の数をエポキシ基の数で除した値(活性水素の数/エポキシ基の数)を、シール剤中のエポキシ系化合物由来のエポキシ基の数に対する、シール剤中の熱硬化剤由来の活性水素の数の比率として算出した。
上述の液晶滴下工法用シール剤を、ディスペンサー(武蔵エンジニアリング製、ショットマスター)を用いて、透明電極と配向膜が予め形成された40mm×45mmガラス基板(RT-DM88-PIN、EHC社製)上に、38mm×38mmの四角形(枠状)に塗布し、シールパターン(断面積2500μm2)を形成した。次いで、シールパターンを形成したガラス基板に対して垂直になるように、対になるガラス基板を減圧下で貼り合せた後、大気開放して貼り合わせた。そして、貼り合わせた2枚のガラス基板を1分間遮光ボックス内で保持した後、3000mJ/cm2の可視光を含む光(波長370~450nmの光)を照射し、さらに120℃で1時間加熱してシールを硬化させた。
◎:25N/mm以上で剥離
〇:15N/mm以上、25N/mm未満で剥離
×:15N/mm未満で剥離
ヤング率の測定と同様に硬化フィルムを作製した。吸湿剤として塩化カルシウム(無水)を封入したアルミカップに硬化フィルムを乗せ、さらにアルミリングを乗せてねじ締をした。その後、アルミカップ全体の初期の質量を計測した。そして、60℃90%Rhに設定した恒温槽にアルミカップを入れて、24時間放置した。そして、アルミカップを取り出して質量を計測した。得られた質量を、計算式「透湿量=(試験後質量-試験前重量)*フィルム厚み/(フィルム面積×100)」に入れて、透湿量を算出した。得られた値を、以下の基準で評価した。
◎:70g/m2未満
〇:70以上150g/m2未満
×:150g/m2以上
シール剤をプラスチック製のシリンジに抜取り、E型粘度計により25℃、2.5rpmの条件で初期の粘度(粘度:A)を測定した。一方、シール剤(シリンジ)を23℃の恒温槽に168時間保管した後、再度粘度(粘度:B)を測定した。得られた粘度について、粘度増加率を以下の計算式で算出し、以下の基準で評価した。なお、粘度増加率が100%に近いほど粘度安定性が高いことを示す。
粘度増加率(%)=B/A×100
〇:粘度増加率が120%以下
×:粘度増加率が120%超
得られたシール剤を10ccのシリンジに充填した後、脱泡し、続いてディスペンサー(ショットマスター:武蔵エンジニアリング社製)に充填した。このディスペンサーを用いて、ガラス基板に毎秒4cmのスピードで塗布し描画を行なった。塗布性は以下の基準で評価した。
○:所望の描画線からのシール剤の染み出しまたは糸曳きが無く、かつ外観も良好
△:前記染み出しまたは糸曳きは無いが、外観が不良
×:前記染み出しまたは糸曳きが発生し塗布適性が極めて不良
Claims (19)
- 液晶滴下工法に使用する、液晶滴下工法用シール剤であって、
前記液晶滴下工法用シール剤を厚み100μmの膜状にし、3000mJ/cm2の光を照射し、120℃で1時間加熱してフィルムを形成したとき、
動的粘弾性測定装置で測定される、前記フィルムの120℃における初期ヤング率が1.0×108Pa以下であり、かつ
前記フィルムを121℃、100%Rh環境下で24時間保存後に動的粘弾性測定装置で測定される、前記フィルムの120℃におけるPCT後ヤング率と、前記初期ヤング率との差が、8.0×107Pa以下である、
液晶滴下工法用シール剤。 - 前記硬化性モノマーの分子量が700以上である、
請求項2に記載の液晶滴下工法用シール剤。 - 前記重合性化合物の総量に対する前記硬化性モノマーの総量が、10質量%以上30質量%以下である、
請求項2に記載の液晶滴下工法用シール剤。 - (メタ)アクリル系熱可塑性ポリマー粒子をさらに含み、
前記(メタ)アクリル系熱可塑性ポリマー粒子の量が、10質量%以上である、
請求項2に記載の液晶滴下工法用シール剤。 - イミダゾール系熱潜在性硬化剤、アミンアダクト系熱潜在性硬化剤、およびポリアミン系熱潜在性硬化剤からなる群より選ばれる少なくとも一種の熱硬化剤をさらに含む、
請求項2に記載の液晶滴下工法用シール剤。 - 重合性官能基を有する重合性化合物と、熱硬化剤と、を含む液晶滴下工法用シール剤であって、
前記重合性化合物がエポキシ系化合物を含み、
前記液晶滴下工法用シール剤中の前記エポキシ系化合物由来のエポキシ基の数に対する、前記液晶滴下工法用シール剤中の前記熱硬化剤由来の活性水素の数の比率が0.25以上であり、
前記液晶滴下工法用シール剤を厚み100μmの膜状にし、3000mJ/cm2の光を照射し、120℃で1時間加熱してフィルムを形成したとき、
動的粘弾性測定装置で測定される、前記フィルムの120℃における初期ヤング率が1.0×108Pa以下であり、かつ
前記フィルムを121℃、100%Rh環境下で24時間保存後に動的粘弾性測定装置で測定される、前記フィルムの120℃におけるPCT後ヤング率と、前記初期ヤング率との差が、8.0×107Pa以下である、
液晶滴下工法用シール剤。 - 前記硬化性モノマーの分子量が700以上である、
請求項8に記載の液晶滴下工法用シール剤。 - 前記重合性化合物の総量に対する前記硬化性モノマーの総量が、10質量%以上30質量%以下である、
請求項8に記載の液晶滴下工法用シール剤。 - 硬化触媒をさらに含み、
前記硬化触媒の融点が100℃以上である、
請求項7に記載の液晶滴下工法用シール剤。 - 無機粒子からなるコアと、前記コアを覆うポリマー層とを有する被覆粒子をさらに含み、
前記被覆粒子は、表面にエポキシ基および/または炭素-炭素二重結合を含む官能基を有する、
請求項7に記載の液晶滴下工法用シール剤。 - 前記ポリマー層が、架橋型ポリマーを含む、
請求項12に記載の液晶滴下工法用シール剤。 - 前記被覆粒子の平均粒子径が0.2μm~10μmである、
請求項12に記載の液晶滴下工法用シール剤。 - 一対の基板の一方の基板上に、請求項1~14のいずれか一項に記載の液晶滴下工法用シール剤を塗布し、シールパターンを形成する工程と、
前記シールパターンが未硬化の状態において、前記一方の基板の前記シールパターンの領域内、または他方の基板上に液晶を滴下する工程と、
前記一方の基板と前記他方の基板とを、前記シールパターンを介して重ね合わせる工程と、
前記シールパターンを硬化させる工程と、
を含む、液晶表示パネルの製造方法。 - 前記シールパターンを硬化させる工程において、前記シールパターンに光を照射する、
請求項15に記載の液晶表示パネルの製造方法。 - 前記光が、可視光を含む、
請求項16に記載の液晶表示パネルの製造方法。 - 前記シールパターンを硬化させる工程において、光を照射後、加熱する、
請求項16または17に記載の液晶表示パネルの製造方法。 - 請求項1~14のいずれか一項に記載の液晶滴下工法用シール剤の硬化物を含む、
液晶表示パネル。
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