WO2019208756A1 - Gap sealant composition for display device, and method for manufacturing display device and display device using same - Google Patents
Gap sealant composition for display device, and method for manufacturing display device and display device using same Download PDFInfo
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- WO2019208756A1 WO2019208756A1 PCT/JP2019/017859 JP2019017859W WO2019208756A1 WO 2019208756 A1 WO2019208756 A1 WO 2019208756A1 JP 2019017859 W JP2019017859 W JP 2019017859W WO 2019208756 A1 WO2019208756 A1 WO 2019208756A1
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- Prior art keywords
- display device
- gap
- bezel
- component
- composition
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/56—Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
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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
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- G—PHYSICS
- G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
- G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
- G09F9/00—Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements
Definitions
- the present invention relates to a gap sealant composition for a display device that can be suitably used for the purpose of filling a gap between a bezel and a display panel, particularly when manufacturing a display device such as a liquid crystal display device and a touch panel.
- a manufacturing method of a display device using the gap sealant composition for the display device, and a structure in which a gap between the bezel and the display panel is filled with the gap sealant composition The present invention also relates to a display device with further improved display quality and durability.
- display devices equipped with a front panel such as a touch panel or a decorative panel have been increasing for liquid crystal display modules as display devices.
- the touch panel is an input interface component.
- the decorative panel is tempered glass or the like printed for decoration from the viewpoint of design and display surface protection.
- These display devices are generally composed of a backlight unit, a display panel, a bezel and a front panel arranged so as to sandwich the bezel, and in recent years, with the miniaturization of display panels, diversification of installation locations and designs, There is a tendency to design narrower bezels.
- air gap bonding even when the outer periphery of the rectangular front panel and the display module is bonded to each other with an air layer therebetween (hereinafter referred to as “air gap bonding” for the sake of convenience), the display quality deteriorates due to the entry of foreign matter into the display surface. Has become an issue. Therefore, in this case as well, there is a demand not only for simply attaching the front panel to the display module but also for improving the display quality by some means.
- OCR optical elastic resin
- the formation of the resin member is a so-called “blading purpose”, and in the optical carburizing, a dam-like resin member made of the same or similar material as the OCR is provided in the gap between the bezel and the display panel at the opening end.
- the height of the gap between the bezel and the display panel varies due to the swell of the bezel, and the resin member covers the entire gap area before the resin member is temporarily cured with UV or the like in a large gap. It cannot be sealed and may be partially biased (this phenomenon is called “sink”). As a result, a normal resin member is not formed, and a gap remains between the resin member and the open end, and the OCR may penetrate into the display module from the gap. On the other hand, in a portion where the gap is small, the resin member itself may flow into and penetrate into the back side of the bezel before being temporarily cured with UV or the like.
- the OCR soaked inside the display module is not cured by UV light for curing, so it does not cure over time and spreads to all gaps in the display module, eroding the back of the display panel and the backlight shining surface.
- cause display failure, or uncured OCR leaks from the display module, causing deterioration in appearance and product durability, and in the worst case, it cannot be used as a product ( deterioration in yield). Bring.
- the resin member is formed so as to straddle the surface facing the front panel of the bezel, but a small amount of the resin member cannot sufficiently close the gap, If a large amount of resin material is used, the area of the resin material spreads beyond the limited area on the light-shielding film from the opening edge to the display area, and the original display area is eroded by the resin material, resulting in poor display.
- the light-shielding film region that can be applied also becomes narrow.
- Patent Document 2 it is difficult to design the gap sufficiently with a resin member that reaches the height of the bezel, or such a first resin member / second resin member is actually provided. However, depending on the design of the display panel, it may cause an unacceptable level of display unevenness depending on the display performance.
- the gap between the bezel of the display device and the display panel is reliably filled to serve as a squint. Even when OCR is injected, the OCR is inserted into the display module from the gap. There is a strong demand for a gap sealant that can reliably prevent internal penetration.
- the present inventors discovered a new subject in the process of solving the said subject.
- Patent Document 1 or Patent Document 2 an ultraviolet curable resin is applied as a dam agent, and thereafter, the dam agent is cured by irradiating ultraviolet rays from a spot UV light source to form a resin member.
- the curable resin is injected under the bezel, so that light is structurally easily blocked and sufficient ultraviolet rays or the like are irradiated. It may not be possible.
- the present inventors fill the gap between the bezel of the display device and the display panel, which does not cause a problem of poor curing even when a curable resin is injected into the gap, or does not cause a problem of poor curing. As a result, a new problem has been recognized that a gap sealant composition suitable for the purpose is required.
- the present invention has been made to solve the above-described problems, and even when injected under the bezel, it does not substantially cause a problem due to poor curing, and is arranged in a recent trend of small size / space saving. Therefore, it can be sufficiently applied to the design of a display device that adopts a narrow bezel width (that is, a narrow light-shielding film region), and even if there is a variation in the gap between the bezel and the display panel in the display device, Providing a gap sealant composition for a display device that enables opto-carbonization by OCR by striking the gap with an easy and efficient means and effectively suppressing the OCR from penetrating into the display module from the gap. It is something to try.
- the present invention intends to provide a high-quality and high-reliability display device having improved display performance and durability by using the gap sealant composition for display device, and a method for producing the same. is there.
- the present inventors have [1] (A) one or more organopolysiloxanes having a curing reactive functional group in the molecule, And (B) a liquid containing a curing reaction catalyst and having an initial viscosity at 25 ° C. in the range of 100 to 100,000 mPa ⁇ s, and forming a non-flowable reactant within at least 30 minutes at the same temperature.
- the present inventors have found that the above problems can be solved by a gap sealant composition for a display device characterized in that the present invention has been achieved.
- component (A) selected from (A1) organopolysiloxane having a curing reactive group containing a carbon-carbon double bond and (A2) organopolysiloxane having a condensation reactive group
- the gap sealant composition for a display device according to [1] comprising at least polysiloxane.
- Component (A) is (A1) at least an organopolysiloxane having a curing reactive group containing a carbon-carbon double bond, and (A3) an organohydrogenpolysiloxane having a silicon atom-bonded hydrogen atom, Component (B) is (B1) at least a hydrosilylation reaction catalyst,
- Component (B) is (B1-1) a first hydrosilylation reaction catalyst that shows activity in the composition without irradiation with high energy rays, and (B1-2) that does not show activity without irradiation with high energy rays, but has high energy
- a curing reaction catalyst comprising a second hydrosilylation reaction catalyst that is active in the composition upon irradiation with a ray, wherein the mass ratio of component (B1-1) to component (B1-2) is 90/10 to 5/95 Range of When irradiated with high energy rays immediately after preparing the composition, it further has the characteristic of forming a non-flowable reactant within at least 20 minutes at 25 ° C.
- Component (A) is (A1-1) 100 parts by mass of a linear or branched organopolysiloxane having an alkenyl group only at the molecular chain end, (A1-2) An alkenyl group-containing organopolysiloxane having at least one branched siloxane unit in the molecule and having a vinyl (CH2 ⁇ CH—) group content in the range of 1.0 to 5.0 mass% 0-20 parts by mass of resin, (A3-1) A linear or branched organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the molecular chain terminal, in a total of 1 mole of vinyl groups in the components (A1-1) and (A1-2) (A3-2) a linear or resinous organohydrogenpolysiloxane component having at least three silicon-bonded hydrogen atoms in the molecule (A3-2) A1) and an organopolysiloxane containing an amount of silicon-bonded hydrogen atoms of 0
- the component (B) is (B1-1-1) an alkenylsiloxane complex of platinum, and (B1-2-1) (substituted and unsubstituted cyclopentadienyl) trimethylplatinum (IV), ⁇ -diketonatotrimethylplatinum (IV), bis ( ⁇ -diketonate) a curing reaction catalyst containing at least one selected from platinum (II), wherein the mass ratio of the component (B1-1-1) to the component (B1-2-1) is from 90/10 to The gap sealant composition for a display device according to any one of [1] to [5], which is in the range of 5/95.
- Component (A) contains (A2-1) one type or two or more types of organopolysiloxane having a condensation reactive group selected from a hydroxyl group, an alkoxy group, an acyloxy group, and an oximoxy group only at the molecular chain end.
- Organopolysiloxane Component (B) contains (B2) a condensation reaction catalyst, [1] The gap sealant composition for a display device according to any one of [6].
- the component (B) contains (B1-1-1) an alkenylsiloxane complex of platinum, and the platinum content derived from the component (B1-1-1) is in the range of 5 to 30 ppm of the entire composition.
- the gap sealant composition for a display device according to any one of [1] to [7].
- the present inventors have found that the above-mentioned problems can be suitably solved by the following composition from the viewpoint of its usage and characteristics, and have reached the present invention.
- the display device is an image display device including a bezel and a display panel, and is used for the purpose of filling a gap between the bezel and the display panel.
- a reaction material having a storage elastic modulus (G ′) measured at a frequency of 1 hertz using a plate-type dynamic viscoelasticity measuring device of 1000 Pa or more is formed.
- a display device comprising: a display panel having a display surface; and a bezel having a frame portion and an opening end inside the frame portion and covering the display panel side periphery of the display panel with the frame portion.
- a method of manufacturing In at least a part or all of the entire circumference of the opening of the bezel, the gap between the bezel and the display panel is set to an angle at which an injection angle with respect to the gap is in a range of horizontal to 75 degrees [1] to [ 13]
- the manufacturing method of the display apparatus characterized by including the process of inject
- a display panel having a display surface;
- a bezel having a frame portion and an opening end inside the frame portion, and covering the periphery of the display panel side of the display panel with the frame portion;
- the present invention there is substantially no problem due to poor curing even when injected under the bezel, and a narrow bezel width (that is, a narrow light-shielding film) for placement in a compact / space-saving trend that is a recent trend.
- This can be applied sufficiently in the design of display devices adopting the area), and even if there is a variation in the gap between the bezel and the display panel in the display device, this gap is surely secured by an easy and efficient means for industrial production.
- the gap sealant composition for a display device it is possible to provide a high-quality and high-reliability display device with improved display performance and durability, and a method for manufacturing the display device.
- FIG. 3 is a partial cross-sectional view illustrating the display device of Embodiment 1.
- FIG. 1 is an exploded perspective view showing a display device of Embodiment 1.
- FIG. 3A is a partial cross-sectional view illustrating a manufacturing process in which a resin member is injected from the horizontal direction into the gap 72 of the display module according to the first embodiment using an L-shaped nozzle.
- FIG. 3B is a partial cross-sectional view showing a structure in which the gap of the display module in Embodiment 1 is filled in the vertical direction with a resin member by horizontal injection.
- FIG. 4A is a resin for the purpose of filling the gap 72 in the vertical direction in advance because it suppresses the variation in the size of the gap 72 of the display module in Embodiment 1 and is used as the starting point / end point of the curable resin to be injected later. It is a fragmentary sectional view which shows the state which has arrange
- FIG. 4B is a partial cross-sectional view illustrating a state in which a resin member is injected into the gap 72 of the display module in Embodiment 1 in advance in order to fill the gap 72 in the vertical direction and the gap 72 is adjusted in the vertical direction.
- FIG. 5 is a partial cross-sectional view showing a manufacturing process in which a resin member is injected from the vertical direction into the gap 72 of the display module in the comparative embodiment using a nozzle.
- gap sealant composition for display device First, the gap sealant composition for display devices of the present invention will be described.
- room temperature or “room temperature” is 25 ° C.
- the “reactant” is a thickened body, a solid or a semi-solid material formed as a result of the progress of a curing reaction between the components of the liquid gap sealant composition.
- thermoplastic solids that exhibit fluidity when heated to solid, elastic solids, and heat (eg, heating at 100 ° C. or higher) but are non-flowable at 25 ° C. are included.
- these reactants may be cured reactants in which the curing reaction is substantially completed, and have two or more stages of multi-curability (particularly, including secondary curability and tertiary curability).
- the reaction product may be a curing reaction product, or a semi-cured product in the course of the curing reaction.
- the “reacted product” in the present invention is a cured product in which the curing reaction is substantially completed, at least one stage of curing reaction is substantially completed, but a cured product having further curing reactivity, cured It may be any semi-cured product in which the reaction is not substantially completed but thickening or solidification is in progress. Moreover, the said semi-hardened
- cured material may be equipped with the multi-stage curability of 2 steps or more.
- the scale of the display device which is one of the main technical effects of the present invention, depends on the fluidity of the liquid composition at room temperature and in a short time regardless of the degree of the curing reaction and the presence or absence of multi-curability of the reactant. This is because it is realized by a change in physical properties.
- non-flowable means that it is not at least liquid and does not substantially deform or flow in an unloaded state, and preferably does not deform or flow in an unloaded state at 25 ° C. Means that.
- a reactant preferably has a storage elastic modulus (G ′) of 1000 Pa or more measured at a frequency of 1 hertz using a cone plate or parallel plate type dynamic viscoelasticity measuring apparatus.
- G ′ storage elastic modulus
- the reactant having non-fluidity as a result of the progress of thickening or curing, a gel-like or solid (including elastic body and thermoplastic) reactant is formed, and the viscosity of the reactant It is preferable that the measurement is substantially difficult.
- the reactant is non-flowable, at least one stage of curing reaction may not be substantially completed, and if the fluidity is lost due to surface thickening or curing, The curing reaction does not have to proceed in the deep part. This is because, if the reactant is non-fluid, the scale of the display device, which is one of the main technical effects of the present invention, is achieved.
- the “initial viscosity” is a mixed viscosity of the entire composition immediately after the composition is prepared by mixing each component, and can be measured using a rheometer or the like. That is, the gap sealant composition for a display device according to the present invention is a multi-component type composition (particularly including a two-component type) prepared by mixing each component before use. Preferably, immediately after mixing of the multi-components, it is liquid and in a certain viscosity range, so that it can be injected into the gap of the display device.
- the gap sealant composition for a display device of the present invention comprises (A) one or more types of organopolysiloxane having a curing reactive functional group in the molecule, And (B) a liquid containing a curing reaction catalyst and having an initial viscosity at 25 ° C. in the range of 100 to 100,000 mPa ⁇ s, and forming a non-flowable reactant within at least 30 minutes at the same temperature. It is characterized by doing.
- the composition of the present invention is characterized by its curing profile. That is, immediately after mixing each component, the initial viscosity at 25 ° C. is in the range of 100 to 100000 mPa ⁇ s. Therefore, using a dispenser equipped with an L-shaped nozzle / needle, etc. Can be injected into the gap between the bezel and the display panel, while forming a non-flowable reactant at 25 ° C. within at least 30 minutes to achieve the void-clad or fast-curing curing. It has a profile.
- the initial viscosity may be in the range of 500 to 50000 mPa ⁇ s, more preferably in the range of 750 to 30000 mPa ⁇ s, and particularly preferably in the range of 1000 to 25000 mPa ⁇ s in practice. If the initial viscosity is less than the lower limit, even in a fast-curing or quick-drying curing profile, the fluidity is high, so that there are cases where outflow to the display module side after injection or in particular poor filling in the vertical direction may occur. . On the other hand, if the initial viscosity exceeds the upper limit, thickening / curing may proceed excessively during the pouring operation, and sufficient pot life in the pouring process may not be ensured.
- the composition may be a non-fluid reactant at any time before 30 minutes (for example, 15 minutes, 20 minutes, 25 minutes, etc.), and after 30 minutes or more. Further, the curing reaction may proceed.
- the storage elastic modulus (G ′) measured at a frequency of 1 hertz using a cone plate or parallel plate type dynamic viscoelasticity measuring apparatus is 1000 Pa or more.
- the time required for the composition according to the present invention to be in the state of a non-flowable reactant or the above storage elastic modulus (G ′) to reach a value of 1000 Pa or more depends on the components (A) and (B ) Can be designed or controlled by appropriately selecting the type and amount of the composition or by selecting the type and amount of an inhibitor for the curing system of the composition (for example, a curing inhibitor for the curing system including a hydrosilylation reaction). It is.
- component (B) when the curing reaction proceeds in the presence of component (B) at room temperature in the presence of component (A), the amount of component (B) is increased and no inhibitor for component (B) is added, or until injection
- component (B) when the curing reaction proceeds in the presence of component (B) at room temperature in the presence of component (A), the amount of component (B) is increased and no inhibitor for component (B) is added, or until injection
- the composition according to the present invention needs to maintain a liquid state and ensure a pot life in the step of injecting into the gap of the display device, particularly the gap between the bezel and the display panel.
- the timing at which the composition according to the present invention is formed can be selected, for example, by storing the composition in a multi-component form such as two liquids and mixing it at the time of injection.
- each component may be mixed with a mixer or the like immediately before injection, loaded into a dispenser within the pot life, and injected into a desired site.
- the present invention can be smoothly implemented.
- a dispenser having a liquid raw material tank physically provided with a partition and a mechanism for mixing a predetermined amount of liquid raw material supplied from each raw material tank to the discharge unit may be used.
- a dispenser having a tank mechanism and a mixing mechanism that can separate and load the raw material liquid, each component of the composition according to the present invention is loaded into a physically partitioned tank, It is also possible to mix and discharge a certain amount at the time of dispensing.
- compositions can be formed and injected into a desired site so that the time lag between discharge and mixing is virtually zero, even if the pot life of the composition after mixing is short
- the composition and the method for producing a display device according to the present invention can be carried out without any problem. That is, since the composition according to the present invention can select the mixing means and the timing of injection, securing the pot life at room temperature is an optional factor.
- a dispenser having such a structure is commercially available. For example, a dispenser in which a discharge nozzle is provided in a plastic double cartridge manufactured by MIX-PAC can be exemplified.
- composition concerning this invention contains the following component (A) and component (B).
- Component (A) is one or more organopolysiloxanes having a curing reactive functional group in the molecule, and may include any of the following organopolysiloxanes or a combination thereof.
- curing reactive functional group of component (A) examples include any curing reactive functional group such as a hydrosilylation reactive group, a radical reactive group, a condensation reactive functional group, and in particular, a carbon-carbon double bond.
- curing reactive functional group such as a hydrosilylation reactive group, a radical reactive group, a condensation reactive functional group, and in particular, a carbon-carbon double bond.
- Preferred examples thereof include hydrosilylation reactive groups or radical reactive groups; hydrosilylation reactive groups that are silicon-bonded hydrogen groups; and condensation reactive groups selected from hydroxyl groups, alkoxy groups, acyloxy groups, and oximoxy groups.
- the radical reactive group includes a high energy ray reactive group such as ultraviolet rays.
- Component (A) may be an organopolysiloxane containing one kind of curing reactive group in the molecule, or an organopolysiloxane containing two or more different kinds of curing reactive groups in the molecule. Alternatively, it may be a mixture of organopolysiloxanes different from each other in the kind of curing reactive functional group / bonding site / content / siloxane skeleton.
- component (A) particularly preferably, (A1) an organopolysiloxane having a curing reactive group containing a carbon-carbon double bond, (A2) Organopolysiloxane having a condensation reactive group, and (A3) organohydrogenpolysiloxane having a silicon atom-bonded hydrogen atom are exemplified, and one or more kinds of organos selected from component (A1) and component (A2)
- a composition containing at least polysiloxane is preferred in the present invention.
- the composition containing the component (A1) is cured by a hydrosilylation reaction or a radical reaction.
- the composition containing the component (A2) is cured by a condensation reaction.
- the component (A) of the composition according to the present invention is preferably hydrosilylation reaction curable, and an organopolysiloxane mixture containing both the component (A1) and the component (A3) is preferable.
- Component (A1) is an organopolysiloxane having a curing reactive group containing a carbon-carbon double bond, vinyl group, allyl group, butenyl group, pentenyl group, hexenyl group, heptenyl group, octenyl group, nonenyl group, C2-C20 alkenyl group such as decenyl group, undecenyl group, dodecenyl group; acrylic-containing group such as 3-acryloxypropyl group, 4-acryloxybutyl group; 3-methacryloxypropyl group, 4-methacryloxybutyl Examples thereof include linear, branched, cyclic, or resinous (network-like) organopolysiloxanes containing a curing reactive group selected from methacryl-containing groups such as groups in the molecule.
- the organopolysiloxane as the component (A1) may contain a group selected from a monovalent hydrocarbon group, a hydroxyl group and an alkoxy group having no carbon-carbon double bond in the molecule. Moreover, in the monovalent hydrocarbon group, a part of the hydrogen atoms may be substituted with a halogen atom or a hydroxyl group. Examples of such monovalent hydrocarbon groups include methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and the like.
- Alkyl group Alkyl group; phenyl group, tolyl group, xylyl group, naphthyl group, anthracenyl group, phenanthryl group, pyrenyl group and other aryl groups; benzyl group, phenethyl group, naphthylethyl group, naphthylpropyl group, anthracenylethyl group, phenane
- An aralkyl group such as a tolylethyl group or a pyrenylethyl group; and a hydrogen atom of these aryl groups or aralkyl groups; an alkyl group such as a methyl group or an ethyl group; an alkoxy group such as a methoxy group or an ethoxy group; a chlorine atom or a bromine atom; And a group substituted with a halogen atom.
- a component (A1) contains a hydroxyl group etc., the said
- component (A1) has the following average composition formula: R 1 a R 2 b SiO (4-ab) / 2 Or a mixture thereof.
- R 1 is a curing reactive group containing the above carbon-carbon double bond
- R 2 is a group selected from a monovalent hydrocarbon group having no carbon-carbon double bond, a hydroxyl group and an alkoxy group
- a and b are numbers satisfying the following conditions: 1 ⁇ a + b ⁇ 3 and 0.001 ⁇ a / (a + b) ⁇ 0.33, preferably, the following conditions: 1.5 ⁇ a + b ⁇ 2.5 and It is a number that satisfies 0.005 ⁇ a / (a + b) ⁇ 0.2.
- the component (A1) is Component (A1) is (A1-1) a linear or branched organopolysiloxane having an alkenyl group only at the molecular chain end, and (A1-2) optionally having at least one branched siloxane unit in the molecule,
- Component (A1-1) has (Alk) R 2 2 SiO 1/2 at the molecular chain end. (Wherein Alk is an alkenyl group having 2 or more carbon atoms), and the other siloxane units are substantially composed only of siloxane units represented by R 2 2 SiO 2/2. It is a linear or branched organopolysiloxane. R 2 represents the same group as described above. Further, the degree of siloxane polymerization of the component (A1-1) is in the range of 7 to 1002, including the terminal siloxane unit. Such component (A1-1) is particularly preferably a linear organopolysiloxane in which both ends of the molecular chain are blocked with siloxane units represented by (Alk) R 2 2 SiO 1/2. is there.
- Component (A1-2) is an alkenyl group-containing organopolysiloxane resin, Average unit formula: (RSIO 3/2 ) o (R 2 SiO 2/2 ) p (R 3 SiO 1/2 ) q (SiO 4/2 ) r (XO 1/2 ) s
- R is a group selected from an alkenyl group and the monovalent hydrocarbon group having no carbon-carbon double bond
- X is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms.
- R is an alkenyl group in a range where the content of vinyl (CH2 ⁇ CH—) group in the organopolysiloxane resin satisfies the range of 1.0 to 5.0% by mass.
- at least a part of R on the siloxane unit represented by RSiO 1/2 is preferably an alkenyl group.
- (o + r) is a positive number
- p is 0 or a positive number
- q is 0 or a positive number
- s is 0 or a positive number
- p / (o + r) is 0 to 10
- Q / (o + r) is a number in the range 0-5
- (o + r) / (o + p + q + r) is a number in the range 0.3-0.9
- s / (o + p + q + r) is a number in the range of 0 to 0.4.
- the composition as a whole can be cured quickly. It is possible to provide a gap sealant composition for a display device that is excellent in properties / fast drying properties, gives a cured reaction product excellent in mechanical strength and flexibility, and is particularly suitable for gap seal applications in display devices.
- Component (A3) is an organohydrogenpolysiloxane having silicon-bonded hydrogen atoms, and preferably has at least two silicon-bonded hydrogen atoms in the molecule and functions as a crosslinking agent for component (A1). It is an ingredient.
- 1,1,3,3-tetramethyldisiloxane, 1,3,5,7-tetramethylcyclotetrasiloxane tris (dimethylhydrogensiloxy) methylsilane, tris (dimethylhydrogen) Siloxy) phenylsilane, trimethylsiloxy group-capped methylhydrogen polysiloxane with molecular chain at both ends, trimethylsiloxy group-capped dimethylsiloxane / methylhydrogensiloxane copolymer with molecular chain at both ends, dimethylhydrogensiloxy group-capped dimethylpoly with molecular chain at both ends Siloxane, molecular chain both ends dimethylhydrogensiloxy group-blocked dimethylsiloxane / methylhydrogensiloxane copolymer, molecular chain both ends trimethylsiloxy group-blocked methylhydrogensiloxane / diphenylsiloxane copolymer, It
- the component (A3) is (A3-1) a linear or branched organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the molecular chain end, and optionally (A3-2) at least three silicon-bonded hydrogen atoms in the molecule
- a linear or resinous organohydrogenpolysiloxane having the following formula is included.
- Component (A3-1) is an organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the molecular chain end, and functions as a chain extender in the hydrosilylation reaction with component (A1), and is a cured reaction product. It is a component that improves the flexibility.
- Such component (A3-1) is preferably a linear organohydrogenpolysiloxane, and those represented by the following structural formula can be preferably used.
- Me and Ph represent a methyl group and a phenyl group, respectively, m1 is a number from 1 to 100, and n1 is a number from 1 to 50.
- Component (A3-2) is a linear or resinous organohydrogenpolysiloxane having at least three silicon-bonded hydrogen atoms in the molecule. When used in combination with component (A3-1) above, It is a component that realizes rapid curability in the composition.
- linear organohydrogenpolysiloxanes trimethylsiloxy group-capped methylhydrogen polysiloxanes at both molecular chain ends, trimethylsiloxy group-capped dimethylsiloxane / methylhydrogensiloxane copolymers with both molecular chain terminals, and dimethylhydrol at both molecular chain terminals.
- the resinous organohydrogenpolysiloxane comprises at least a branched siloxane unit selected from an SiO 4/2 unit (Q unit) and an R 3 SiO 3/2 unit (T unit), and R 3 3 SiO 1 / 2 units (M units), R 3 2 HSiO 1/2 units ( MH units), and optionally R 3 2 SiO 1/2 units (D units), R 3 HSiO 1/2 units ( DH units)
- M units M units
- R 3 2 SiO 1/2 units R 3 HSiO 1/2 units
- DH units Comprising M H MQ type, M H Q type, M H MT type, M H T type, M H MQT type, M H QT type, M H MDQ type, M H MDD H Q type, M H DQ type, M H DD H Q type, MH MDT type, MH MDD H T type, MH DT type, MH DD H T type, MH MDQT type, MH MDD H QT type, MH DQT type,
- the content of component (A3) is preferably such that the number of silicon-bonded hydrogen atoms in the composition is preferably 0 with respect to 1 mole of carbon-carbon double bonds in component (A1).
- the amount is in the range of 1 to 10 mol, preferably in the range of 0.2 to 5.0 mol, particularly preferably in the range of 0.5 to 2.0 mol. Amount. If the content of the component (A3) is below the lower limit, it may cause poor curing. If the content of the component (A3) exceeds the upper limit, the mechanical strength of the cured product becomes too high, and the elastic body or A gel-like cured reaction product may not be obtained.
- the component (A) is particularly preferably With respect to component (A1) containing 100 parts by weight of the above component (A1-1) and 0 to 20 parts by weight of the above component (A1-2), Component (A3-1) An amount such that silicon-bonded hydrogen atoms are 0.1 to 10 moles relative to a total of 1 mole of vinyl groups in components (A1-1) and (A1-2), preferably An amount of 0.2 to 5.0 mol, more preferably an amount of 0.5 to 2.0 mol, and the above component (A3-2) components (A1-1) and (A1-2)
- the amount of silicon-bonded hydrogen atoms is 0 to 1 mol, preferably 0 to 0.5 mol, more preferably 0.1 to 0.5 mol with respect to 1 mol of the total vinyl groups therein. It contains an organopolysiloxane in a molar
- the component (A) may be (A2) an organopolysiloxane having a condensation reactive group, and in particular, a condensation selected from the above hydroxyl group, alkoxy group, acyloxy group, and oximoxy group. It may be an organopolysiloxane (A2-1) containing one or more types of organopolysiloxane having a reactive group only at the molecular chain end.
- a condensation-reactive component (A2) may be used in combination with a hydrosilylation-reactive organopolysiloxane such as the above-mentioned component (A1), and a large amount of condensation reaction catalyst is used as the curing agent (B) described later.
- the quick curing / quick drying curing profile necessary for the present invention may be designed only by the component (A2).
- Component (B) is a curing reaction catalyst, and is a component that causes the curing reaction to proceed with respect to the curing reactive functional group of component (A).
- component (B) include a hydrosilylation reaction catalyst, a photopolymerization initiator, a peroxide, or a condensation reaction catalyst.
- a hydrosilylation reaction catalyst or a condensation reaction catalyst For convenience of use as a gap sealant composition for a display device, Since it is often difficult to irradiate a large amount of high energy rays, it is preferable to include a hydrosilylation reaction catalyst or a condensation reaction catalyst.
- the component (A) includes the component (A1), preferably both the component (A1) and the component (A2), and is cured by a hydrosilylation reaction. In the case of having a group, it is a component that causes a curing reaction to proceed.
- (B1-1) a first hydrosilylation reaction catalyst that shows activity in the composition without irradiation with high energy rays, and optionally (B1-2) shows no activity without irradiation with high energy rays.
- a curing reaction catalyst comprising a second hydrosilylation reaction catalyst that is active in the composition by irradiation with high energy rays, wherein the mass ratio of the component (B1-1) to the component (B1-2) is 100/0 Those in the range of ⁇ 5/95 are preferred.
- examples of the high energy rays include ultraviolet rays, X-rays, and electron beams. Among these, ultraviolet rays are preferable from the viewpoint of efficiency of catalyst activation.
- the irradiation amount varies depending on the type of the high energy ray active catalyst, but in the case of ultraviolet rays, the integrated irradiation amount at a wavelength of 365 nm is preferably within a range of 100 mJ / cm 2 to 10 J / cm 2.
- Component (B1-1) is the first hydrosilylation catalyst that shows activity in the present composition without irradiation with high energy rays.
- the component is a hydrosilylation reaction catalyst that gives a fast curing / fast drying curing profile necessary for the composition when it contains no hydrosilylation reaction inhibitor or in a small amount. Examples include rhodium-based catalysts, palladium-based catalysts, nickel-based catalysts, iridium-based catalysts, ruthenium-based catalysts, and iron-based catalysts, and platinum-based catalysts are preferred.
- Platinum-based compounds such as platinum fine powder, platinum black, platinum-supported silica fine powder, platinum-supported activated carbon, chloroplatinic acid, chloroplatinic acid alcohol solution, platinum olefin complex, platinum alkenylsiloxane complex, etc.
- platinum alkenylsiloxane complexes are preferred.
- alkenylsiloxane examples include 1,3-divinyl-1,1,3,3-tetramethyldisiloxane, 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane, Examples thereof include alkenyl siloxanes in which part of the methyl groups of these alkenyl siloxanes are substituted with ethyl groups, phenyl groups, and the like, and alkenyl siloxanes in which the vinyl groups of these alkenyl siloxanes are substituted with allyl groups, hexenyl groups, and the like.
- 1,3-divinyl-1,1,3,3-tetramethyldisiloxane is preferred because the stability of this platinum-alkenylsiloxane complex is good. Further, since the stability of the platinum-alkenylsiloxane complex can be improved, 1,3-divinyl-1,1,3,3-tetramethyldisiloxane and 1,3-diallyl-1,1 are added to this complex.
- Component (B1-1) is a catalyst that shows activity without irradiation with high energy rays, and among them, a catalyst that shows activity even at a relatively low temperature is preferable. Specifically, it exhibits activity in the composition in the temperature range of 0 to 200 ° C., and accelerates the hydrosilylation reaction.
- the content of component (B1-1) varies depending on the type of catalyst and the type of composition, but usually the metal atoms in the catalyst are within the range of 0.01 to 50 ppm by mass relative to the composition.
- the (B1-1-1) platinum alkenylsiloxane complex is used so that the platinum content is preferably in the range of 1.5 to 30 ppm. / It is particularly preferable from the viewpoint of quick drying. If the amount of component (B1-1) added is too small, the object of the present invention of fast curability cannot be achieved. If the amount added is too large, the pot life is too short, resulting in practical inconveniences. It is an economy.
- Component (B1-2) is a second hydrosilylation catalyst that exhibits activity in the present composition when irradiated with high energy rays, but does not exhibit activity without irradiation with high energy rays.
- the so-called activating catalyst or photoactivated catalyst is a second hydrosilylation catalyst that exhibits activity in the present composition when irradiated with high energy rays, but does not exhibit activity without irradiation with high energy rays.
- component (B1-2) include (methylcyclopentadienyl) trimethylplatinum (IV), (cyclopentadienyl) trimethylplatinum (IV), (1,2,3,4,5-pentamethyl (Cyclopentadienyl) trimethylplatinum (IV), (cyclopentadienyl) dimethylethylplatinum (IV), (cyclopentadienyl) dimethylacetylplatinum (IV), (trimethylsilylcyclopentadienyl) trimethylplatinum (IV), (Methoxycarbonylcyclopentadienyl) trimethylplatinum (IV), (dimethylphenylsilylcyclopentadienyl) trimethylcyclopentadienylplatinum (IV), trimethyl (acetylacetonato) platinum (IV), trimethyl (3,5- Heptanedionate) platinum (IV), trimethyl (methylacetate) Cetate) platinum (IV), bis (2,4-
- the component (B1-2) is an optional component in the present composition, but the reaction product obtained by the component (B1-1) is subjected to secondary curability (hereinafter referred to as “photocuring” by irradiation with high energy rays.
- photocuring secondary curability
- the curing reaction can proceed further in the non-fluid region, and further curing reaction can proceed, and further faster curing / fast drying compared to (B1-1) alone. Can be realized.
- the content thereof is an amount necessary to further cure the composition to the reaction product obtained by the component (B1-1) or an amount sufficient to improve fast curability / fast dryness, preferably
- the amount of the metal atom in the catalyst is in the range of 1 to 50 ppm, preferably in the range of 5 to 30 ppm, with respect to the present composition.
- the mass ratio of the component (B1-1) to the component (B1-2) is preferably in the range of 90/10 to 5/95, and 85/15 A range of ⁇ 10 / 90 is more preferred. If the mass ratio is less than or equal to the upper limit, the curing reaction can be accelerated by irradiation with high energy rays, and if the mass ratio is less than the lower limit, the curing reaction at a low temperature such as room temperature in a short time does not proceed. That is, the fast curing / fast drying curing profile required for the composition may not be realized.
- ultraviolet irradiation can be performed by irradiating the periphery of the composition after inject
- the composition according to the present invention was irradiated with a high energy ray immediately after the composition was prepared. In some cases, it can be designed to further have the characteristic of forming a non-flowable reactant within at least 20 minutes at 25 ° C. Even when such a composition is injected under a bezel or the like where it is difficult to efficiently irradiate high energy rays, the composition can be further rapidly irradiated with light using a spot UV light source or the like. It is extremely useful when using the gap sealant composition for a display device according to the present invention in that it can realize excellent curability and quick drying.
- the irradiation timing and irradiation amount of the high energy beam are arbitrary, and when using the actual composition, the high energy beam may be irradiated immediately after the preparation, or after a certain time, Needless to say, high energy rays may be irradiated. Further, the practical irradiation amount and the irradiation amount for defining the above-mentioned characteristics are as described above, but the actual use is not limited to this.
- the composition according to the present invention preferably does not contain a hydrosilylation reaction inhibitor.
- a hydrosilylation reaction inhibitor is added to the composition.
- the composition can be obtained by adding a hydrosilylation reaction inhibitor. This is because it is preferable that the curing reaction of the product is not delayed.
- a necessary minimum amount of hydrosilylation reaction inhibitor may be added.
- the component (B) when the component (A) has a condensation reactive group, the component (B) may contain (B2) a condensation reaction catalyst.
- a catalyst for the condensation reaction is not limited, and examples thereof include organic tin compounds such as dibutyltin dilaurate, dibutyltin diacetate, tin octenoate, dibutyltin dioctate, tin laurate; tetrabutyl titanate, tetrapropyl titanate, dibutoxybis ( Organic titanium compounds such as ethyl acetoacetate; other acidic compounds such as hydrochloric acid, sulfuric acid and dodecylbenzenesulfonic acid; alkaline compounds such as ammonia and sodium hydroxide; 1,8-diazabicyclo [5.4.0] undecene (DBU) )
- An amine compound such as 1,4-diazabicyclo [2.2.2] octane (DABCO) is exempl
- the amount of component (B2) used is that required to give the composition a fast cure / fast dry cure profile required.
- the component (B2) can be used arbitrarily as long as the component (B1) can achieve the required fast curing / drying curing profile.
- the reaction is particularly effective. Curing in the deep part of the object may progress with time, and the eye-tightening effect may be further improved as a gap filler composition of a display device.
- composition according to the present invention if necessary, other organopolysiloxanes, adhesion-imparting agents, inorganic fillers such as silica, glass, alumina, and zinc oxide; fine organic resin powders such as polymethacrylate resins; A phosphor, a heat-resistant agent, a dye, a pigment, a flame retardant, a solvent and the like are added to the organopolysiloxane composition used in the present invention.
- the amount of addition and its method are known to those skilled in the art.
- the composition according to the present invention has a fast-curing / fast-drying curing profile, it is preferably a multi-component composition of two or more components.
- the component (A) is a hydrosilylation reaction-curable organopolysiloxane and includes the component (A1) and the component (A3), a multicomponent type of two or more components in which these components are different packages is used. It is preferable to handle it as a composition and mix it immediately before use, or inject it into the gap of the target display device using a dispenser equipped with a mixing mechanism as described above.
- the present composition can be produced by uniformly mixing the above component (A), component (B), and other optional components as necessary at room temperature.
- the component I component contains at least the aforementioned component (A1) and component (B), and optionally includes other components
- the II liquid component contains at least the component (A2),
- Each can be stored for a long period of time by being sealed in a sealed container at room temperature. As described above, immediately after mixing them, it has a liquid and constant initial viscosity and has a fast curing / fast drying curing profile.
- the composition is used as a gap sealant composition for a display device.
- the display device is an image display device including a bezel and a display panel. It is preferable to use the composition for the purpose of filling the gap with the display panel.
- the use for the said objective is the silicone which hardens this composition as a member which has a function which fills the said space
- the composition according to the present invention is preferably cured to form an elastomer (elastic body) resin member or a gel-like resin member.
- the cured silicone resin member is defined by JIS K2220 at 25 ° C.
- the penetration (hereinafter simply referred to as “penetration”) is preferably in the range of 5 to 70, more preferably in the range of 10 to 60 and in the range of 20 to 50. .
- Such a silicone resin member has moderate flexibility and durability, and is excellent in adhesion / adhesion retention and followability between the members. Therefore, it can be reliably used as a gap sealant composition for a display device. It is possible to realize a glazing effect.
- the composition according to the present invention is used for the purpose of filling the gap formed at the overlapping portion of the bezel and the display surface, it is cured and has adhesiveness, and the sample is sufficiently deformed at the maximum adhesive strength. It is preferable to form a large resin member.
- the tensile shear adhesive strength (hereinafter simply referred to as “shear adhesive strength”) measured at 25 ° C. according to JIS K6850 is 0.05 ⁇ MPa.
- the above is preferable, more preferably in the range of 0.05 to 10 MPa, and practically in the range of 0.1 to 5 MPa.
- the displacement ratio is preferably 1000% or more.
- the proportion is preferably in the range of 1000 to 6000%.
- the present invention relates to a display device manufacturing method and a display device characterized by the use of the gap sealant composition for a display device described above.
- a display device 203 includes a display panel 10 having a display surface 11, a frame portion 21 and an opening end 22 inside the frame portion 21, and the display surface of the display panel 10.
- a bezel 20 whose peripheral edge on the 11 side is covered with a frame portion 21, a front panel 30 provided with the bezel 20 sandwiched between the display surface 11 side of the display panel 10, and an opening end 22 of the bezel 20.
- OCR 50 is provided.
- the display surface 11 refers to the entire surface of the polarizing plate 12 on the front panel 30 side (the same applies hereinafter).
- a CF substrate 13 and a TFT substrate 14 are provided to face each other via a liquid crystal (not shown), and polarizing plates 12 and 15 are provided on the outer side of the CF substrate 13 and the outer side of the TFT substrate 14, respectively.
- 10 is configured.
- the display panel 10 is mounted on the backlight unit 71, and the bezel 20 and the backlight unit 71 are fixed by a fitting structure (not shown), whereby the display module 70 is configured.
- the entire surface of the display module 70 and the front panel 30 such as a touch panel is bonded via the OCR 50.
- the resin member 40 is provided so that the gap 72 generated in the overlapping portion between the bezel 20 and the display surface 11 does not have a gap in the direction perpendicular to the display surface 11.
- the resin member 40 is provided only in the overlapping portion between the bezel 20 and the display surface 11, the display area 18 is not substantially affected, and the bezel 20 has a narrow structure. However, it does not cause display unevenness in the completed display device, and the display quality, in particular, the display quality and operability in the region close to the end of the bezel are improved. Further, since the resin member 40 fills the bezel 20 and the display surface 11 in the vertical direction without gaps, the overflow of the OCR 50 is effectively suppressed and the purpose of so-called “sticing” is reliably achieved, and the display device It is possible to improve the durability of the product, reduce the incidence of defective products during production, and further improve the yield and display quality.
- the resin member 40 has a structure in which the bezel 20 and the display surface 11 are filled in the vertical direction without a gap, and does not have a structure straddling the display region 18 or the bezel 20.
- the display area 18 can be maximized while no projections or uneven structures derived from the resin member 40 are formed on the bezel 20, so that the resin member proposed in Patent Document 2 or the like is placed on the bezel 20.
- unevenness and dimensional (height) variations on the bezel are less likely to occur, and the distance between the surface 23 of the bezel 20 and the front panel 30 in FIG. 2 can be kept constant.
- the front panel 30 is arranged with high flatness by the adhesive member 60 disposed on the outer periphery of the bezel 20, and it is possible to prevent the appearance defect and the adhesion failure from occurring.
- the resin member 40 filling the gap 72 under the bezel 20 has a reliable weathering effect, the OCR 50 does not overflow the display panel 10 or the backlight unit 71.
- the display device according to the first embodiment has a gap sealant for a display device according to the present invention at an angle with respect to the gap 72 in the range of horizontal to 75 degrees. It can be obtained by a method for manufacturing a display device including a step of injecting and filling the composition.
- a method for manufacturing a display device including a step of injecting and filling the composition.
- Patent Document 2 when the injection angle with respect to the gap 72 is in the vertical direction, as shown in FIG. 5, the gap 72 generated at the overlapping portion of the bezel 20 and the display surface 11 is closed from the outside.
- the scale is insufficient and the OCR 50 overflows to the bottom of the display panel 10 or the backlight unit 71. This is verified in a reference example with respect to an example described later.
- an L-shaped, substantially L-shaped or flexible discharge port is used as a means for injecting the gap sealant composition for the display device at an angle with which the injection angle is horizontal to 75 degrees with respect to the gap 72.
- a step of injecting a gap sealant composition for a display device with an injection angle that is substantially horizontal ( 0 degree).
- an injection device provided with such an L-shaped nozzle or the like for example, a syringe or a dispenser provided with an L-shaped needle (Musashi Curve Needle CPN-18G-A90 manufactured by Musashi Engineering Co., Ltd.) is commercially available.
- the discharge port is substantially formed with respect to the gap 72 by a dispenser device having an L-shaped nozzle on the display surface 11 of the display panel 10 along the opening end 22 of the bezel 20.
- the gap sealant composition for the display device is injected at a constant speed and in a constant amount so as to be horizontally oriented (FIG. 3A), and UV light is emitted from the spot UV light source so as to follow the injection path of the dam material. Irradiation was performed to form the resin member 40 inside the gap 72 formed at the overlapping portion of the bezel 20 and the display surface 11 (FIG. 3B).
- the gap sealant composition for a display device according to the present invention has a fast-curing / fast-drying curing profile, a non-flowable reactant is formed before irradiation with UV light.
- the object may be further cured by irradiation with UV light, and irradiation with UV light may be omitted.
- injecting the curable resin composition to be a dam material it is particularly preferable to inject at a constant speed and in a constant amount with the tip of the L-shaped nozzle inserted inside the gap 72.
- the gap sealant composition for a display device that can be used for the purpose of filling a gap formed at the overlapping portion of the bezel and the display surface and the curing means thereof are as described above. Yes, it can be cured in a short time and does not adversely affect each component of the display device. From the standpoint of not adversely affecting each member of the display device, photo-curing by UV light irradiation (including the use of photoreactive hydrosilylation catalyst) It is preferable to select a curing system in which is the main curing means.
- the dimensions of the display device of Embodiment 1 are not particularly limited, and the design dimension from the open end of the bezel to the display area is 0.1 to 10 mm, preferably 0.2 to 5 mm. It is common to do.
- the display module 70 has a design dimension of 1.5 mm from the open end 22 of the bezel 20 to the display area 18, whereas the gap 72 between the display panel 10 and the bezel 20 is 0.2 mm and the thickness of the bezel 20 is The thickness may be designed in the range of 0.3 mm.
- the actual size of the gap 72 that is, the distance from the display surface 11 of the display panel 10 to the surface 23 of the bezel 20 varies greatly when the bezel 20 is placed on the display panel as it is.
- the gap sealant composition for a display device When the gap sealant composition for a display device is injected at a constant speed and in a fixed amount, it may cause a filling failure in the gap 72. If there is such a filling defect, the gap 72 cannot be sufficiently closed, and a gap is generated. Therefore, after the OCR is injected, the OCR penetrates into the display module from the gap and leaks, and the display quality deteriorates. Or the durability of the display device may be reduced.
- the gap 72 in order to inject the gap sealant composition for the display device so that the discharge port is substantially horizontal with respect to the gap 72, the gap 72 is closed from the vertical direction (FIG. 5, patent). Such a filling failure is less likely to occur compared to Document 1 or Patent Document 2).
- the following display device in order to more surely fill the gap between the bezel and the display panel and perform reliable filling, the following display device is manufactured. The method can be suitably employed.
- the two are not arranged as they are, but in advance between the bezel and the display panel in the direction perpendicular to the display panel.
- the gap sealant composition is injected and filled to eliminate or reduce the variation in the gap height between the bezel and the display panel. Can do.
- Such a member has a physical or chemical affinity to the injected gap sealant composition in addition to the function of keeping the height between the members constant. Leakage can be prevented and more effective weathering can be realized by using as a starting point or an ending point at the time of filling.
- Such a member may be a resin member obtained by curing the same or different curable resin composition as the resin member filled in the gap between the bezel and the display panel, and both are for the display device according to the present invention.
- a silicone resin member obtained by curing the gap sealant composition is preferred. Since these resin members have a function of adjusting the height of the gap between the two members when the bezel having waviness is arranged on the display panel, the resin member has a function of adjusting the height of the gap. Preferably, three or more points are more preferable, and four or more points are particularly preferable. Most preferably, the resin member has four corners or at least four points arranged on substantially diagonal lines.
- the starting point at the time of injection When the uncured curable resin composition injected from the discharge port comes into contact with the resin member placed at the end point (including the intermediate point), the interface between the two has good affinity for interfacial tension In addition, it spreads uniformly in the entire region of the gap into which the curable resin composition has been injected and is less likely to be biased, so that filling defects associated with so-called “shrinkage” are effectively suppressed.
- a gap between the bezel and the display panel is previously provided in a direction perpendicular to the display panel.
- the gap between the bezel and the display panel is set to a horizontal to 75 degree injection angle with respect to the gap on the entire periphery of the opening of the bezel. It includes the step of injecting and filling the gap sealant composition for a display device of the present invention at an angle within a range.
- the resin member provided for the purpose of filling the gap between the members in the vertical direction with respect to the display panel without any gap is a display surface on the display panel, and when the bezel is disposed, In the entire circumference of the part, it is preferable to provide four points or more on each of the four corners or the longitudinal and lateral axes. After the holding material made of these resin members is provided on the display surface, the bezel having the waviness is arranged to effectively adjust the distance from the display surface of the display panel to the surface of the bezel, that is, the height of the gap.
- the leakage in the vertical direction is effectively suppressed, and the starting point or the ending point at the time of injection Since it functions, it can suppress that the gap sealing agent composition inject
- the gap sealant composition of the present invention is injected into the gap at a constant speed and in a constant amount at an injection angle of ⁇ 75 degrees in the horizontal direction, filling defects in the gap are further suppressed, and reliable filling is achieved. .
- a resin member 41 which is a holding material made of a resin member (a gap sealant composition for a display device of the present invention) is arranged in advance (FIG. 4A), and the bezel 20 is arranged in a state where the height is held by the holding material. (FIG. 4B).
- the gap sealant of the present invention can be obtained by pre-adjusting the height of the same gap 72 at one or more points on the four corners or each side, for a total of four or more points.
- the composition is injected into the gap at a constant speed and in a fixed amount at an injection angle of ⁇ 75 degrees in the horizontal direction, filling defects in the gap are further suppressed, and reliable filling is achieved.
- the curable resin composition used for forming the resin member that is the gap holding material is not particularly limited, and the curable resin composition that is the dam material. May be the same as or different from those exemplified. From the viewpoint of simplicity of the working process, a curable silicone resin composition of the same kind as that preferably exemplified as the gap sealant composition may be used and is preferable.
- the height of the resin member as the holding material is substantially the same at each point.
- the resin member obtained by curing the curable resin composition can be selected from an adhesive and an elastic body or a gel-like cured product.
- an elastic body or a gel-like cured product By using such an elastic body or a gel-like cured product, the resin member Even if the heights are somewhat uneven, there is an advantage that the resin member is deformed when arranged on the resin member of the bezel, and the overall gap height is adjusted to be substantially the same.
- the manufacturing method and display device further have a structure in which a display panel and a front panel are bonded together using a curable resin composition that is OCR, and a process related thereto.
- the silicone resin member formed by curing the gap sealant composition for a display device reliably achieves the cover for the curable resin composition that is OCR, at the time of application or injection of OCR. Since OCR leaks from the gap and penetrates into the display module, it is possible to achieve high display quality and durability in the resulting display device, and to suppress the occurrence of defects during manufacturing, thereby reducing yield. Can be improved.
- Embodiment 1 of the present invention after filling the gap 72 with the resin member 40, the OCR 50 is applied over the entire surface, the adhesive 60 is applied over the entire outer periphery of the bezel 20, and the touch panel as the front panel 30 is placed in a reduced pressure environment. After the whole surface is bonded, it is fully cured by UV irradiation.
- the display device 101 shown in FIG. 2 is completed by such a series of manufacturing processes.
- the manufacturing process of the display device 101 according to the first embodiment excludes the step of filling the gap 72 by the resin member 40, which is the dam material, and the step of preliminarily adjusting the height of the gap 72 with a holding material. Is equivalent to a general optocarbonizing process, and has versatility as an optocarbonizing process of a display device.
- the gap sealant composition for a display device that forms the resin member that is a dam material and the resin member that is a holding material for the gap 72 is UV-irradiated simultaneously with the application.
- UV irradiation may be performed after coating the entire circumference. In some cases, UV temporary curing itself is not necessary.
- these resin members are formed directly under the bezel 20, that is, outside the display region.
- Patent Document 1 Problems such as the fact that the boundary is easily visually recognized due to the difference in refractive index from the OCR used for optical carving are essentially solved. That is, the display quality and performance are deteriorated due to the refractive index difference between the OCR and the resin member disposed for the purpose of closing the gap 72, which has been a problem in the prior art (Patent Document 1 or Patent Document 2).
- the present invention provides an essential solution to this problem.
- the OCR coating process in the case of optical carburizing
- the bonding process required for manufacturing a display device having a front panel is limited to the above-described reduced pressure environment.
- a known bonding method under an atmospheric pressure environment may be employed.
- OCR is applied to the front panel in an atmospheric pressure environment, and the front panel is inverted and bonded to the display module (reverse bonding method), or a predetermined gap is secured between the front panel and the display module.
- a method of arranging them in parallel and filling OCR between the gaps may be used.
- the gap 72 between the opening end 22 and the display panel 10 is completely covered by the resin member 40, and the resin member 40 is formed under the bezel 20, so that Since the dam is not broken in the process and the uncured OCR 50 does not leak into the display module 70, the display device 101 with high display reliability can be provided. Further, since the resin member 40 does not reach the display area, there is a problem of display quality and display performance degradation such as display unevenness at an end portion resulting from a difference in refractive index from the OCR, and a decrease in operability derived therefrom. The problem is essentially solved.
- the distance between the opening end 22 and the gap 72 between the display panel 10 is previously held constant by the resin member 41 that is a holding material, and injected. Even if the gap sealant composition is injected into the gap 72 at a constant and constant speed, it can improve the affinity for the gap sealant composition for the display device and function as a starting point / end point at the time of injection. Reliable weathering can be achieved, and industrial productivity is excellent. Further, since the resin member 40 is formed under the bezel 20, when the front panel 30 is disposed on the bezel 20, the unevenness derived from the resin member 40 used for the cover does not occur, and the front panel It is possible to prevent poor appearance and poor adhesion at the time of attachment.
- the display panel 10 and the front panel 30 in the first embodiment have a structure in which the entire surface is bonded by OCR, the structure is bonded with an air layer (air gap bonding). You may change to
- the adhesive member 60 is disposed on the bezel 20. This is because when the external force F in the peeling direction is applied to the OCR 50 on the display surface 11, the front panel 30 and the OCR 50 are peeled off. The purpose is to improve resistance. As a result, even when the front panel 30 having a larger outer shape than the display module 70 is bonded, it is possible to reliably reinforce the adhesive so that the OCR 50 on the display surface 11 is not stressed. . In addition, it is desirable from the viewpoint of reinforcement that the adhesive strength of the adhesive member 60 is stronger than that of the OCR 50. However, if the adhesive member 60 is equal to or more than the OCR 50, a certain reinforcing effect can be obtained.
- the display device has a structure in which a space between the display surface and the front panel is filled with a substantially transparent optical elastic resin member or optical gel resin member.
- a display device is preferred.
- OCR optical elastic resin member
- the display performance and durability of the display device can be improved, and a highly reliable display device can be provided.
- Such an OCR is preferably formed by curing a curable resin composition, and has physical properties relating to a ratio of displacement with respect to a sample thickness at the above-described penetration, shear adhesive strength, and maximum adhesive strength, and UV.
- the silicone resin hardened material (member) formed by photocuring including light irradiation is illustrated.
- Such OCR is not particularly limited, but is commercially available from Toray Dow Corning / Dow Corning, EG-1200, EG-4131, VE-6001600UV, etc .; manufactured by Wacker, SilGel 612 PT, LUMISIL 100, LUMISIL 102 Is available.
- the gap sealant composition of the present invention may be used as an OCR, and may minimize differences in physical properties such as refractive index and hardness of the two, or may further improve adhesion and sealing properties. is there.
- the display device further includes: A shield substrate provided on a surface of the front panel facing the display surface and having a surface on which a transparent conductive film is formed;
- the display device may include a structure in which the transparent conductive film and the bezel are electrically connected via a conductive material.
- a shield substrate such as an EMI (Electro-Magnetic Interference) substrate provided with a conductive layer on one side between the display module 70 and the front panel 30.
- EMI Electro-Magnetic Interference
- a conductive layer made of a transparent conductive film such as ITO (Indium Tin Oxide) is formed uniformly or in a mesh shape on one side of the shield substrate.
- ITO Indium Tin Oxide
- the bezel 20 of the display module 70 is made of metal and is GND-connected in the display module 70.
- the adhesive member 60 as a conductive material, the metal bezel 20 and the conductive layer of the shield substrate can be reliably connected to the GND, so that a display device with high electromagnetic wave resistance can be provided.
- the present invention has been described with reference to the above embodiment, the present invention is not limited to each of the above embodiments. Various changes that can be understood by those skilled in the art can be made to the configuration and details of the present invention. Further, the present invention includes a combination of some or all of the configurations of the above-described embodiments as appropriate.
- the UV curable case has been described as the OCR for whole surface bonding.
- the present invention is not limited to this, and the same applies to the case of a thermosetting type, a moisture curable type, or a composite curable type thereof.
- the effect is obtained.
- a further dam material is provided outside the silicone resin member that fills the gap between the bezel and the display panel as a dam material, and a part of the gap or It does not preclude taking a structure that covers everything. For example, if the design uses a special shape for a part of the bezel and the gap cannot be completely closed even if the above method is used, the curable resin composition that is a dam material at the point is pinpointed. Things may be injected.
- the shape of the front panel is a square shape
- it is not necessary to be a square shape, it may be any polygonal shape, a flat plate having a curved portion, or a combination thereof, and moreover, it is a three-dimensional shape. It does not matter.
- the manufacturing method of the display apparatus of this invention is demonstrated in detail by an Example and a comparative example.
- the present invention is not limited to the description of the following examples.
- display devices manufactured according to the following embodiments are included in the scope of the present invention, but the display devices of the present invention are not limited to the description of the following embodiments.
- SiH (CE) / Vi For a linear or branched organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the end of the molecular chain, a silicon bond with respect to a total of 1 mole of vinyl groups in other components Moles of hydrogen atoms SiH (XL) / Vi: For a linear or resinous organohydrogenpolysiloxane having at least three silicon-bonded hydrogen atoms in the molecule, silicon is added to a total of 1 mol of vinyl groups in other components.
- Double viscosity arrival time Immediately after the preparation of the composition, at 25 ° C., the viscosity was measured every minute using a TA Instruments rheometer (AR550), and the time when it reached twice the initial viscosity ( Minutes). The viscosity was a value at Shearrate 20 (1 / s).
- ⁇ Penetration After 2 hours or more have passed and the curing reaction is practically complete, the cured silicone resin member is defined in JIS K2220 at 25 ° C. using PENETROMETER RPM-101 manufactured by Kouaisha. The penetration was measured.
- G'1000 Pa arrival time Immediately after the preparation of the composition, using a rheometer manufactured by TA Instruments (AR550) at 25 ° C., using a cone plate with a diameter of 20 mm as a geometry, and a frequency of 1 Hz, 1 The storage elastic modulus G ′ was measured every minute, and the time (minute) at which G ′ of the reaction product reached 1000 Pa was recorded. In addition, the measurement was performed in the same manner when there was ultraviolet irradiation (with light irradiation). ⁇ Check for fluidity after 30 minutes: Immediately after each composition was uniformly mixed with a static mixer at room temperature, it was discharged into a horizontal plate shape, allowed to stand at 25 ° C.
- Gap sealant for display device (cured product) with a sample thickness of 200 ⁇ m obtained by curing each composition is bonded in a range of 25 mm ⁇ 25 mm square between two glass plates, and a universal material test from both sides Using a machine (manufactured by Shimadzu Corp., Autograph AGS-1kNG), the peak value of the shear adhesive strength (MPa) was measured by pulling in the horizontal direction at a test speed of 100 mm / min. Further, the value obtained by multiplying the horizontal displacement at the peak value of the shear adhesive force (MPa) in the same test by the sample thickness (200 ⁇ m) multiplied by 100 is shown in Table 1 as the shear adhesive elongation (%). It was described in.
- the comparative examples 1 to 9 corresponding to the examples 1 to 9 differ in the content of the hydrosilylation reaction catalyst, particularly the content of the component (b1-1-1) having hydrosilylation reaction activity at 25 ° C.
- the amount of platinum is large, immediately after mixing, it is a liquid composition having an initial viscosity in the range of 1100 to 21000 mPas, and the time to reach twice the initial viscosity is in the range of 3 to 14 minutes. Therefore, while having a sufficient pot life, a non-flowable reactant was given within 30 minutes.
- Examples 5 to 7 and 9 containing a photoactive platinum catalyst a more rapid curing reaction was realized by using ultraviolet irradiation together, and a non-flowable reactant was formed within 20 minutes.
- 1.7 mm high spacers are provided at the four corners of the display part A to provide a gap with the bezel B, and the bezel B is adhered and cured to the display part A by the method of the example and the comparative example.
- Example 10 The above-mentioned gap sealant composition for display device of Example 5 (hereinafter referred to as “UV curable adhesive”) was mixed into a Musashi clear syringe PSY-10E while mixing with a static mixer, and an auto dispenser (Musashi Engineering Co., Ltd.). Set to company SHOTMASTER 300 DS-S) and fitted with 18G standard needle.
- Table 3 shows the accuracy of mounting the front panel, that is, the presence or absence of non-uniformity in the gap between the bezel and the front panel due to the application of the UV curable adhesive in relation to the experimental conditions.
- Example 10 in which a UV curable adhesive was injected at a constant speed from the horizontal direction into the gap using an L-shaped needle with respect to the gap, starting from the adhesive (resin member) obtained by The model test proved that it is possible to manufacture a display device with excellent reliability without causing leakage of the OCR and poor mounting of the front panel.
- the present invention is not limited to liquid crystal displays, and can be used in the field of display displays such as organic EL displays, electronic paper displays, plasma displays, and the like.
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Abstract
Description
本発明は、液晶表示装置、タッチパネル等の表示装置の製造時、特に、ベゼルと表示パネル間の空隙を充填する目的に好適に使用可能な表示装置用のギャップシール剤組成物に関する物であり、当該表示装置用のギャップシール剤組成物を用いることを特徴とする表示装置の製造方法、および当該ギャップシール剤組成物によりベゼルと表示パネル間の空隙が充填された構造を備え、製造時の歩留まり、表示品質および耐久性等がさらに改善された表示装置に関する。 The present invention relates to a gap sealant composition for a display device that can be suitably used for the purpose of filling a gap between a bezel and a display panel, particularly when manufacturing a display device such as a liquid crystal display device and a touch panel. A manufacturing method of a display device using the gap sealant composition for the display device, and a structure in which a gap between the bezel and the display panel is filled with the gap sealant composition The present invention also relates to a display device with further improved display quality and durability.
近年、表示デバイスとしての液晶表示モジュールに対し、タッチパネルや加飾パネルなどの前面パネルを搭載した、表示装置が増加してきている。タッチパネルは、入力インターフェース部品である。加飾パネルは、デザイン性や表示面保護の観点から加飾のために印刷が施された強化ガラス等である。これらの表示装置は、一般的に、バックライトユニット、表示パネル、ベゼルおよびベゼルを挟むように配置された前面パネルからなり、近年、表示パネルの小型化、設置場所およびデザインの多様化に伴い、ベゼルの幅をより狭く設計する傾向にある。 In recent years, display devices equipped with a front panel such as a touch panel or a decorative panel have been increasing for liquid crystal display modules as display devices. The touch panel is an input interface component. The decorative panel is tempered glass or the like printed for decoration from the viewpoint of design and display surface protection. These display devices are generally composed of a backlight unit, a display panel, a bezel and a front panel arranged so as to sandwich the bezel, and in recent years, with the miniaturization of display panels, diversification of installation locations and designs, There is a tendency to design narrower bezels.
前面パネルを液晶表示モジュールに搭載する場合、通常は液晶パネル表面と前面パネルとの間に空気層が存在する。そのため、前面パネル(例えばガラス基板)と空気層との屈折率の違いに起因して、これらの界面で光が反射してしまう。この界面反射によって、特に外光環境下では表示画像の視認性が著しく低下する。これに対し、前面パネルのガラス基板の屈折率に近い屈折率を有する光学弾性樹脂を空気層部分に充填して、液晶パネルと前面パネルとを貼り合せることにより、界面反射を抑えて表示画像の視認性を向上させる技術が提案されている。この全面貼り合せ技術は、オプティカルボンディング(Optical-Bonding)又はダイレクトボンディング(Direct-Bonding)と呼ばれ、光学的な効果だけでなく、前面パネルが割れた場合の飛散防止や耐衝撃性向上といった機械的な効果もあることから、広く採用されるようになってきている。 When a front panel is mounted on a liquid crystal display module, an air layer usually exists between the surface of the liquid crystal panel and the front panel. Therefore, light is reflected at these interfaces due to the difference in refractive index between the front panel (for example, a glass substrate) and the air layer. Due to this interface reflection, the visibility of the displayed image is significantly reduced, particularly in an ambient light environment. On the other hand, an optical elastic resin having a refractive index close to the refractive index of the glass substrate of the front panel is filled in the air layer portion, and the liquid crystal panel and the front panel are bonded together to suppress interface reflection and display images. Technologies for improving visibility have been proposed. This full surface bonding technology is called optical-bonding or direct-bonding, and it is not only an optical effect but also a machine that prevents scattering and improves impact resistance when the front panel breaks. Because of its effects, it has been widely adopted.
また、四角形状の前面パネルと表示モジュールとの空気層を隔てた外周貼り合せ(以下、便宜上「エアギャップボンディング」と呼ぶ。)であっても、表示面内への異物侵入による表示品質の低下が課題となっている。そのため、この場合も、単純に表示モジュールに前面パネルを貼り付けるだけではなく、何らかの工夫による表示品質の向上が求められている。 In addition, even when the outer periphery of the rectangular front panel and the display module is bonded to each other with an air layer therebetween (hereinafter referred to as “air gap bonding” for the sake of convenience), the display quality deteriorates due to the entry of foreign matter into the display surface. Has become an issue. Therefore, in this case as well, there is a demand not only for simply attaching the front panel to the display module but also for improving the display quality by some means.
たとえば、特許文献1および特許文献2では、表示モジュールに枠状に樹脂部材(=ダム材)を形成し、その内側に光学弾性樹脂(以下「OCR(Optically Clear Resin)」という。)を塗布し、その上から前面パネルを貼り合せることを提案している。この場合、樹脂部材の形成は、いわゆる「目張り目的」であり、オプティカルボンディングにおいては、開口端でのベゼルと表示パネルとの間隙に、OCRと同一又は類似の材料からなるダム状の樹脂部材を形成することにより、OCRが間隙から表示モジュール内にしみ込むことを防止しようとするものである。
For example, in Patent Document 1 and
しかしながら、このような樹脂部材は表示領域(画素領域)にかかってしまうと表示ムラとして視認され、特に表示面の端部における表示品質の劣化に直結するため、開口端から表示領域までの間の遮光膜上という限られた領域内に形成する必要があり、大量のダム材で目張りを行うことは実際の装置構成では極めて困難である。 However, when such a resin member is applied to the display area (pixel area), it is visually recognized as display unevenness, and in particular, it leads directly to deterioration of display quality at the end of the display surface. It is necessary to form it in a limited area on the light shielding film, and it is extremely difficult to carry out the screening with a large amount of dam material in an actual apparatus configuration.
さらに、ベゼルのうねりに由来して、ベゼルと表示パネルとの間隙の高さにばらつきが生じ、間隙の大きな部分では、樹脂部材をUV等で仮硬化させる前に、樹脂部材が間隙全領域を封止できず、一部に偏ってしまうことがある(この現象を「ひけ」と呼ぶ。)。この結果、正常な樹脂部材が形成されず、樹脂部材と開口端とに隙間が残った状態となり、OCRがその隙間から表示モジュールの内部にしみ込んでしまう場合がある。一方、間隙の小さな部分では、樹脂部材自体が、UV等で仮硬化させる前に、ベゼルの裏面側に流れてしみ込んでしまう場合がある。表示モジュールの内部にしみ込んだOCRは、硬化のためのUV光が当たらないため時間が経っても硬化せず、表示モジュール内のあらゆる隙間に広がってゆき、表示パネル裏面やバックライト昭光面を侵食して表示不良を引き起こしたり、未硬化のOCRが表示モジュールから漏洩し、外観の悪化、製品耐久性の低下の原因となったり、最悪の場合、製品として利用できない(=歩留まりの悪化)という不具合をもたらす。 Furthermore, the height of the gap between the bezel and the display panel varies due to the swell of the bezel, and the resin member covers the entire gap area before the resin member is temporarily cured with UV or the like in a large gap. It cannot be sealed and may be partially biased (this phenomenon is called “sink”). As a result, a normal resin member is not formed, and a gap remains between the resin member and the open end, and the OCR may penetrate into the display module from the gap. On the other hand, in a portion where the gap is small, the resin member itself may flow into and penetrate into the back side of the bezel before being temporarily cured with UV or the like. The OCR soaked inside the display module is not cured by UV light for curing, so it does not cure over time and spreads to all gaps in the display module, eroding the back of the display panel and the backlight shining surface. Cause display failure, or uncured OCR leaks from the display module, causing deterioration in appearance and product durability, and in the worst case, it cannot be used as a product (= deterioration in yield). Bring.
さらに、特許文献2の手段においては、第1樹脂部材に加えて、ベゼルの前面パネルに対向する面とを跨ぐように形成された第2樹脂部材を形成することから、ベゼルと表示パネルとの間隙の高さのばらつきに加えて、ベゼル上に樹脂部材の突起部が形成されてしまい、その上に前面パネルを配置する際にベゼル表面の凹凸や接着面の凹凸が生じ、外観不良や表示不良、タッチパネル等においては端部における接触不良/操作感の悪化の原因になる。これに加えて、特に特許文献2の方法では、樹脂部材がベゼルの前面パネルに対向する面とを跨ぐように形成される都合上、少量の樹脂部材では間隙を十分に塞ぐことができない反面、大量に樹脂部材を使うと開口端から表示領域までの間の遮光膜上という限られた領域内を超えて樹脂部材の領域が広がってしまい、本来の表示領域が樹脂部材で侵食され、表示不良を招くという本末転倒な結果を生じるものであるが、近年は、表示パネルの小型化、設置場所およびデザインの多様化に伴い、ベゼルの幅をより狭く設計する傾向があり、このような樹脂部材を塗布可能な遮光膜領域も狭くなる。この結果、特許文献2のように、ベゼル高さまで達するほどの樹脂部材で間隙を十分に塞ぐことが、設計上困難であったり、実際にこのような第1樹脂部材/第2樹脂部材を設けて間隙を塞ごうとすると、表示パネルの設計によっては、その表示性能上、許容できないレベルの表示ムラの原因となる場合がある。
Further, in the means of
以上のように、ベゼルの幅が狭くても、表示装置のベゼルと表示パネル間の空隙を確実に充填して目張りの役割を果たし、OCRを注入しても、OCRが当該隙間から表示モジュールの内部にしみ込むことを確実に防止できるギャップシール剤が強く求められている。 As described above, even when the width of the bezel is narrow, the gap between the bezel of the display device and the display panel is reliably filled to serve as a squint. Even when OCR is injected, the OCR is inserted into the display module from the gap. There is a strong demand for a gap sealant that can reliably prevent internal penetration.
一方、本発明者らは、上記課題を解決する過程で新たな課題を発見した。 On the other hand, the present inventors discovered a new subject in the process of solving the said subject.
近年のトレンドである小型/省スペースに配置するために狭いベゼル幅(すなわち、狭い遮光膜領域)を採用した表示装置の設計において、表示装置のベゼルと表示パネル間の空隙を確実に充填しようとした場合、ベゼルと表示パネル間の空隙内部に、L字型ニードル等を用いて樹脂部材を注入することを本件発明者らは想起した。この場合、空隙を目張りする樹脂部材はベゼル下に配置されることになるので、表示装置の端部における表示ムラ等を発生させることなく、OCRが同間隙から表示モジュール内にしみ込むことを効果的に抑制して、OCRによるオプティカルボンディングを可能にし、その表示性能および耐久性等を改善した高品質かつ高信頼性の表示装置およびその製造方法を提供できることが期待できる。 In designing a display device that adopts a narrow bezel width (that is, a narrow light-shielding film region) for placement in a small / space-saving trend, which is a recent trend, an attempt is made to reliably fill the gap between the display device bezel and the display panel. In this case, the present inventors have recalled that the resin member is injected into the gap between the bezel and the display panel using an L-shaped needle or the like. In this case, since the resin member that covers the gap is disposed below the bezel, it is effective that the OCR penetrates into the display module from the gap without causing display unevenness at the end of the display device. It is expected that a high-quality and high-reliability display device with improved display performance and durability, and a method for manufacturing the same can be provided.
しかしながら、上記の方法を採用した場合、樹脂部材の前駆体である硬化性樹脂を硬化させることが困難になる場合がある。たとえば、前記の特許文献1または特許文献2においては、紫外線硬化性樹脂をダム剤として塗布し、その後にスポットUV光源から紫外線を照射して当該ダム剤を硬化させて樹脂部材を形成させているが、上記のとおり、空隙を目張りする樹脂部材をベゼル下に配置しようとした場合、硬化性樹脂をベゼル下に注入するため、構造的に光が遮られ易く、十分な紫外線等の照射を行うことができない場合がある。また、硬化性樹脂がベゼル下に注入されるタイミングは、必然的に表示モジュール上に設置された後であるため、表示モジュールへの熱の影響を考えると、高温による加熱硬化を行うことは一般に困難であるので室温等の低温硬化性を備えることが望まれる。加えて、硬化性樹脂を所望の部位に注入するためには、未硬化かつ液状の状態であることが必要であるが、ベゼル下に注入された硬化性樹脂が液状のままであると、当該硬化性樹脂が同間隙から流出して表示モジュール内にしみ込む結果となり、目張りの目的が達成されないだけでなく、却って製品不良の原因となる場合がある。また、未硬化かつ液状の状態でベゼル下に留まり、表示モジュールまでしみ込まない場合であっても、当該硬化性樹脂が未硬化の状態であれば、目張りの役割を十分に果たすことができず、後の工程においてOCRを注入した際に、OCRが同間隙から表示モジュール内にしみ込むことを抑制することができない結果となる。
However, when the above method is employed, it may be difficult to cure the curable resin that is the precursor of the resin member. For example, in Patent Document 1 or
以上のように、表示装置のベゼルと表示パネル間の空隙を、当該空隙内部に硬化性樹脂を注入して充填しようとした場合、その構造および製造工程に起因した硬化不良が発生することが懸念されるため、本件発明者らは当該空隙内部に硬化性樹脂を注入しても硬化不良の問題を生じない、あるいは、硬化不良の問題を生じにくい表示装置のベゼルと表示パネル間の空隙を充填する目的に適合したギャップシール剤組成物が求められるという新たな課題の認識に至った。 As described above, when an attempt is made to fill the gap between the bezel of the display device and the display panel by injecting a curable resin into the gap, there is a concern that poor curing due to the structure and the manufacturing process may occur. Therefore, the present inventors fill the gap between the bezel of the display device and the display panel, which does not cause a problem of poor curing even when a curable resin is injected into the gap, or does not cause a problem of poor curing. As a result, a new problem has been recognized that a gap sealant composition suitable for the purpose is required.
すなわち、本発明は、上記課題を解決すべくなされたものであり、ベゼル下に注入しても実質的に硬化不良に伴う問題を生じることがなく、近年のトレンドである小型/省スペースに配置するために狭いベゼル幅(すなわち、狭い遮光膜領域)を採用した表示装置の設計においても十分適用することができ、表示装置におけるベゼルと表示パネルとの間隙のばらつきがあっても、工業生産上容易かつ効率の良い手段でこの間隙を目張りし、OCRが同間隙から表示モジュール内にしみ込むことを効果的に抑制して、OCRによるオプティカルボンディングを可能にする表示装置用ギャップシール剤組成物を提供しようとするものである。 In other words, the present invention has been made to solve the above-described problems, and even when injected under the bezel, it does not substantially cause a problem due to poor curing, and is arranged in a recent trend of small size / space saving. Therefore, it can be sufficiently applied to the design of a display device that adopts a narrow bezel width (that is, a narrow light-shielding film region), and even if there is a variation in the gap between the bezel and the display panel in the display device, Providing a gap sealant composition for a display device that enables opto-carbonization by OCR by striking the gap with an easy and efficient means and effectively suppressing the OCR from penetrating into the display module from the gap. It is something to try.
さらに、本発明は、当該表示装置用ギャップシール剤組成物を用いることにより、その表示性能および耐久性等を改善した高品質かつ高信頼性の表示装置およびその製造方法を提供しようとするものである。 Furthermore, the present invention intends to provide a high-quality and high-reliability display device having improved display performance and durability by using the gap sealant composition for display device, and a method for producing the same. is there.
鋭意検討の結果、本発明者らは、
[1](A)分子内に硬化反応性官能基を有する、1種類以上のオルガノポリシロキサン、
および
(B)硬化反応触媒
を含有してなり、25℃における初期粘度が100~100000mPa・s の範囲の液状であり、さらに、同温度下で少なくとも30分以内に非流動性の反応物を形成することを特徴とする表示装置用のギャップシール剤組成物
により、上記課題を解決できる事を見出し、本発明に到達した。
As a result of intensive studies, the present inventors have
[1] (A) one or more organopolysiloxanes having a curing reactive functional group in the molecule,
And (B) a liquid containing a curing reaction catalyst and having an initial viscosity at 25 ° C. in the range of 100 to 100,000 mPa · s, and forming a non-flowable reactant within at least 30 minutes at the same temperature. The present inventors have found that the above problems can be solved by a gap sealant composition for a display device characterized in that the present invention has been achieved.
また、本発明者らは、組成設計の見地から、以下の組成物により、好適に上記課題を解決できる事を見出し、本発明に到達した。
[2]成分(A)が、(A1)炭素-炭素二重結合を含む硬化反応性基を有するオルガノポリシロキサンおよび(A2)縮合反応性基を有するオルガノポリシロキサンから選ばれる1種類以上のオルガノポリシロキサンを少なくとも含む、[1]に記載の表示装置用のギャップシール剤組成物。
[3]成分(A)が、
(A1)炭素-炭素二重結合を含む硬化反応性基を有するオルガノポリシロキサン、および
(A3)珪素原子結合水素原子を有するオルガノハイドロジェンポリシロキサンを少なくとも含み、
成分(B)が、
(B1)ヒドロシリル化反応触媒を少なくとも含み、
組成物中の炭素-炭素二重結合1モルに対して、珪素結合水素原子が0.1~10モルの範囲にあることを特徴とする、[1]または[2]に記載の表示装置用のギャップシール剤組成物。
[4]成分(B)が、
(B1-1)高エネルギー線の照射なしで、組成物中で活性を示す第一のヒドロシリル化反応触媒、及び
(B1-2)高エネルギー線の照射がないと活性を示さないが、高エネルギー線の照射により組成物中で活性を示す第二のヒドロシリル化反応触媒
を含む硬化反応触媒であり、成分(B1-1)と成分(B1-2)の質量比が90/10~5/95の範囲であり、
組成物を調製した直後に高エネルギー線を照射した場合、25℃で少なくとも20分以内に非流動性の反応物を形成する特徴をさらに有する、
[1]~[3]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
[4-1]高エネルギー線が紫外線であり、波長365nmでの積算照射量が100mJ/cm2~10J/cm2の範囲内である[4]の表示装置用のギャップシール剤組成物。
[5]成分(A)が、
(A1-1)分子鎖末端のみにアルケニル基を有する直鎖状または分岐鎖状のオルガノポリシロキサン 100質量部、
(A1-2)分子内に少なくとも1つの分岐シロキサン単位を有し、ビニル(CH2=CH―)基の含有量が1.0~5.0質量%の範囲内にあるアルケニル基含有オルガノポリシロキサン樹脂 0~20質量部、
(A3-1)分子鎖末端のみに珪素結合水素原子を有する直鎖状または分岐鎖状のオルガノハイドロジェンポリシロキサン 成分(A1-1)および(A1-2)中のビニル基の合計1モルに対して珪素結合水素原子が0.1~10モルとなる量、および
(A3-2)分子内に少なくとも3個の珪素結合水素原子を有する直鎖状または樹脂状のオルガノハイドロジェンポリシロキサン 成分(A1-1)および(A1-2)中のビニル基の合計1モルに対して珪素結合水素原子が0~1モルとなる量
を含有するオルガノポリシロキサンであることを特徴とする、[1]~[4]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
[6]成分(B)が、
(B1-1-1)白金のアルケニルシロキサン錯体、及び
(B1-2-1)(置換および非置換シクロペンタジエニル)トリメチル白金(IV)、βージケトナートトリメチル白金(IV)、ビス(β―ジケトナート)白金(II)から選択される少なくとも1つを含む硬化反応触媒であり、あり、(B1-1-1)成分と(B1-2-1)成分の質量比が90/10~5/95の範囲である、[1]~[5]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
[7]成分(A)が、(A2-1)水酸基、アルコキシ基、アシロキシ基、オキシモキシ基から選ばれる縮合反応性基を分子鎖末端のみに有する1種類または2種類以上のオルガノポリシロキサンを含有するオルガノポリシロキサンであり、
成分(B)が、(B2)縮合反応触媒を含有することを特徴とする、
[1]~[6]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
[8]成分(B)が(B1-1-1)白金のアルケニルシロキサン錯体を含み、当該成分(B1-1-1)に由来する白金含有量が、組成物全体の5~30ppmの範囲にある、[1]~[7]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
Further, the present inventors have found that the above-mentioned problems can be suitably solved by the following composition from the viewpoint of composition design, and have reached the present invention.
[2] One or more organos selected from component (A) selected from (A1) organopolysiloxane having a curing reactive group containing a carbon-carbon double bond and (A2) organopolysiloxane having a condensation reactive group The gap sealant composition for a display device according to [1], comprising at least polysiloxane.
[3] Component (A) is
(A1) at least an organopolysiloxane having a curing reactive group containing a carbon-carbon double bond, and (A3) an organohydrogenpolysiloxane having a silicon atom-bonded hydrogen atom,
Component (B) is
(B1) at least a hydrosilylation reaction catalyst,
The display device according to [1] or [2], wherein a silicon-bonded hydrogen atom is in the range of 0.1 to 10 moles per mole of carbon-carbon double bonds in the composition. Gap sealant composition.
[4] Component (B) is
(B1-1) a first hydrosilylation reaction catalyst that shows activity in the composition without irradiation with high energy rays, and (B1-2) that does not show activity without irradiation with high energy rays, but has high energy A curing reaction catalyst comprising a second hydrosilylation reaction catalyst that is active in the composition upon irradiation with a ray, wherein the mass ratio of component (B1-1) to component (B1-2) is 90/10 to 5/95 Range of
When irradiated with high energy rays immediately after preparing the composition, it further has the characteristic of forming a non-flowable reactant within at least 20 minutes at 25 ° C.
[1] The gap sealant composition for a display device according to any one of [3].
[4-1] The gap sealant composition for a display device according to [4], wherein the high energy ray is ultraviolet light and the integrated irradiation dose at a wavelength of 365 nm is in the range of 100 mJ / cm 2 to 10 J / cm 2 .
[5] Component (A) is
(A1-1) 100 parts by mass of a linear or branched organopolysiloxane having an alkenyl group only at the molecular chain end,
(A1-2) An alkenyl group-containing organopolysiloxane having at least one branched siloxane unit in the molecule and having a vinyl (CH2═CH—) group content in the range of 1.0 to 5.0 mass% 0-20 parts by mass of resin,
(A3-1) A linear or branched organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the molecular chain terminal, in a total of 1 mole of vinyl groups in the components (A1-1) and (A1-2) (A3-2) a linear or resinous organohydrogenpolysiloxane component having at least three silicon-bonded hydrogen atoms in the molecule (A3-2) A1) and an organopolysiloxane containing an amount of silicon-bonded hydrogen atoms of 0 to 1 mole per 1 mole of vinyl groups in (A1-2) [1] The gap sealant composition for a display device according to any one of [4] to [4].
[6] The component (B) is
(B1-1-1) an alkenylsiloxane complex of platinum, and (B1-2-1) (substituted and unsubstituted cyclopentadienyl) trimethylplatinum (IV), β-diketonatotrimethylplatinum (IV), bis ( β-diketonate) a curing reaction catalyst containing at least one selected from platinum (II), wherein the mass ratio of the component (B1-1-1) to the component (B1-2-1) is from 90/10 to The gap sealant composition for a display device according to any one of [1] to [5], which is in the range of 5/95.
[7] Component (A) contains (A2-1) one type or two or more types of organopolysiloxane having a condensation reactive group selected from a hydroxyl group, an alkoxy group, an acyloxy group, and an oximoxy group only at the molecular chain end. Organopolysiloxane
Component (B) contains (B2) a condensation reaction catalyst,
[1] The gap sealant composition for a display device according to any one of [6].
[8] The component (B) contains (B1-1-1) an alkenylsiloxane complex of platinum, and the platinum content derived from the component (B1-1-1) is in the range of 5 to 30 ppm of the entire composition. The gap sealant composition for a display device according to any one of [1] to [7].
また、本発明者らは、その使用方法および特性の見地から、以下の組成物により、好適に上記課題を解決できる事を見出し、本発明に到達した。
[9]表示装置が、ベゼルと表示パネルを備えた画像表示装置であり、当該ベゼルと当該表示パネルとの間隙を充填する目的で使用される、[1]~[8]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
[10][1]~[9]のいずれか1項に記載の表示装置用のギャップシール剤組成物であって、25℃において、組成物の調製後30分以内に、コーン・プレートまたはパラレル・プレート式の動的粘弾性測定装置を用いて振動数1ヘルツで測定される貯蔵弾性率(G’)が1000Pa以上の反応物を形成することを特徴とするもの。
[11]25℃での初期粘度が100~100000mPa・sの範囲であり、さらに、同温度下で少なくとも3分間は、流動性を保つことを特徴とする、[1]~[10]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
[12]硬化物の針入度が5~70の範囲であるシリコーン硬化物を与える、[1]~[11]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
[13]せん断接着強度が0.05 MPa以上で、最大接着強度で試料厚みに対する変位の割合が1000%以上であるシリコーン硬化物を与える、[1]~[12]のいずれか1項に記載の表示装置用のギャップシール剤組成物。
In addition, the present inventors have found that the above-mentioned problems can be suitably solved by the following composition from the viewpoint of its usage and characteristics, and have reached the present invention.
[9] Any one of [1] to [8], wherein the display device is an image display device including a bezel and a display panel, and is used for the purpose of filling a gap between the bezel and the display panel. A gap sealant composition for a display device as described in 1. above.
[10] The gap sealant composition for a display device according to any one of [1] to [9], wherein the cone plate or parallel composition is prepared at 25 ° C. within 30 minutes after the preparation of the composition. A reaction material having a storage elastic modulus (G ′) measured at a frequency of 1 hertz using a plate-type dynamic viscoelasticity measuring device of 1000 Pa or more is formed.
[11] Any one of [1] to [10], wherein the initial viscosity at 25 ° C. is in the range of 100 to 100,000 mPa · s, and the fluidity is maintained for at least 3 minutes at the same temperature. A gap sealant composition for a display device according to claim 1.
[12] The gap sealant composition for a display device according to any one of [1] to [11], which gives a silicone cured product having a penetration of the cured product in the range of 5 to 70.
[13] The display according to any one of [1] to [12], which gives a silicone cured product having a shear adhesive strength of 0.05 MPa or more and a maximum adhesive strength and a displacement ratio with respect to the sample thickness of 1000% or more. A gap sealant composition for an apparatus.
さらに、本発明者は、上記の表示装置用のギャップシール剤組成物を用いた、以下の表示装置の製造方法および表示装置により、好適に上記課題を解決できる事を見出し、本発明に到達した。
[14]表示面を有する表示パネルと、枠部と当該枠部の内側の開口端とを有し、前記表示パネルの前記表示面側の周縁を前記枠部で覆うベゼルとを備えた表示装置を製造する方法であって、
前記ベゼルの前記開口部の全周の少なくとも一部または全部において、前記ベゼルと表示パネルの間の空隙を、当該空隙に対する注入角が、水平~75度の範囲となる角度で
[1]~[13]のいずれか1項に記載の表示装置用のギャップシール剤組成物を注入して充填する工程
を含むことを特徴とする表示装置の製造方法。
[15]前記ベゼルの前記開口部の全周の少なくとも一点以上において、前記ベゼルと表示パネルの間の空隙間に、表示パネルに対して垂直方向に当該空隙を隙間なく充填する機能を有する部材を配置した後に、前記のギャップシール剤組成物を注入して充填する工程を行うことを特徴とする、[14]に記載の表示装置の製造方法。
[16]表示面を有する表示パネルと、
枠部と当該枠部の内側の開口端とを有し、前記表示パネルの前記表示面側の周縁を前記枠部で覆うベゼルと、
前記ベゼルの前記開口部の全周の少なくとも一部または全部において、前記ベゼルと表示パネルの間の空隙が[1]~[13]のいずれか1項に記載の表示装置用のギャップシール剤組成物を硬化させてなる樹脂部材により充填された構造を有する表示装置。
Furthermore, the present inventor has found that the above problems can be suitably solved by the following display device manufacturing method and display device using the gap sealant composition for a display device described above, and has reached the present invention. .
[14] A display device comprising: a display panel having a display surface; and a bezel having a frame portion and an opening end inside the frame portion and covering the display panel side periphery of the display panel with the frame portion. A method of manufacturing
In at least a part or all of the entire circumference of the opening of the bezel, the gap between the bezel and the display panel is set to an angle at which an injection angle with respect to the gap is in a range of horizontal to 75 degrees [1] to [ 13] The manufacturing method of the display apparatus characterized by including the process of inject | pouring and filling the gap sealant composition for display apparatuses of any one of [13].
[15] A member having a function of filling the gap between the bezel and the display panel in a direction perpendicular to the display panel without gaps at least at one point or more of the entire circumference of the opening of the bezel. [14] The method for manufacturing a display device according to [14], wherein a step of injecting and filling the gap sealant composition after the placement is performed.
[16] a display panel having a display surface;
A bezel having a frame portion and an opening end inside the frame portion, and covering the periphery of the display panel side of the display panel with the frame portion;
14. The gap sealant composition for a display device according to any one of [1] to [13], wherein the gap between the bezel and the display panel is at least partly or entirely of the entire periphery of the opening of the bezel. A display device having a structure filled with a resin member obtained by curing an object.
本発明によれば、ベゼル下に注入しても実質的に硬化不良に伴う問題を生じることがなく、近年のトレンドである小型/省スペースに配置するために狭いベゼル幅(すなわち、狭い遮光膜領域)を採用した表示装置の設計においても十分適用することができ、表示装置におけるベゼルと表示パネルとの間隙のばらつきがあっても、工業生産上容易かつ効率の良い手段で確実にこの間隙を塞ぐことができ、OCRが同間隙から表示モジュール内にしみ込むことを効果的に抑制して、OCRによるオプティカルボンディングを可能にする表示装置用ギャップシール剤組成物を提供できる。さらに、当該表示装置用ギャップシール剤組成物を用いることで、その表示性能および耐久性等を改善した高品質かつ高信頼性の表示装置およびその製造方法を提供できる。 According to the present invention, there is substantially no problem due to poor curing even when injected under the bezel, and a narrow bezel width (that is, a narrow light-shielding film) for placement in a compact / space-saving trend that is a recent trend. This can be applied sufficiently in the design of display devices adopting the area), and even if there is a variation in the gap between the bezel and the display panel in the display device, this gap is surely secured by an easy and efficient means for industrial production. It is possible to provide a gap sealant composition for a display device that can be closed and that effectively suppresses OCR from penetrating into the display module from the same gap and enables optocarbonization by OCR. Furthermore, by using the gap sealant composition for a display device, it is possible to provide a high-quality and high-reliability display device with improved display performance and durability, and a method for manufacturing the display device.
[表示装置用ギャップシール剤組成物]
まず、本発明の表示装置用ギャップシール剤組成物について説明する。
[Gap sealant composition for display device]
First, the gap sealant composition for display devices of the present invention will be described.
本発明において「室温」または「常温」とは25℃である。 In the present invention, “room temperature” or “room temperature” is 25 ° C.
本発明において、「反応物」とは、液状のギャップシール剤組成物の成分間における硬化反応が進行した結果、形成された増粘体、固体および半固体状物であり、ゲル状増粘体、ゲル状固体、弾性体状固体および加熱(たとえば、100℃以上の加熱)により流動性を示すが、25℃では非流動性である熱可塑体を特に含む。さらに、これらの反応物は、硬化反応が実質的に完結した硬化反応物であってもよく、2段階以上の多次硬化性(特に、二次硬化性および三次硬化性を含む)を備えた硬化反応性の反応物であってもよく、硬化反応の途上にある半硬化物の状態であってもよい。すなわち、本発明における「反応物」は硬化反応が実質的に完結した硬化物、少なくとも一段階以上の硬化反応が実質的に完結しているが、更なる硬化反応性を備えた硬化物、硬化反応が実質的に完結していないが増粘乃至固体化が進行する途上にある半硬化物のいずれであってもよい。また、前記の半硬化物は、2段階以上の多次硬化性を備えていてもよい。本発明の主要な技術的効果の一つである表示装置の目張りは、硬化反応の程度および反応物の多次硬化性の有無に関わらず、室温かつ短時間における液状組成物の流動性にかかる物性変化により実現されるものであるからである。 In the present invention, the “reactant” is a thickened body, a solid or a semi-solid material formed as a result of the progress of a curing reaction between the components of the liquid gap sealant composition. In particular, thermoplastic solids that exhibit fluidity when heated to solid, elastic solids, and heat (eg, heating at 100 ° C. or higher) but are non-flowable at 25 ° C. are included. Furthermore, these reactants may be cured reactants in which the curing reaction is substantially completed, and have two or more stages of multi-curability (particularly, including secondary curability and tertiary curability). The reaction product may be a curing reaction product, or a semi-cured product in the course of the curing reaction. That is, the “reacted product” in the present invention is a cured product in which the curing reaction is substantially completed, at least one stage of curing reaction is substantially completed, but a cured product having further curing reactivity, cured It may be any semi-cured product in which the reaction is not substantially completed but thickening or solidification is in progress. Moreover, the said semi-hardened | cured material may be equipped with the multi-stage curability of 2 steps or more. The scale of the display device, which is one of the main technical effects of the present invention, depends on the fluidity of the liquid composition at room temperature and in a short time regardless of the degree of the curing reaction and the presence or absence of multi-curability of the reactant. This is because it is realized by a change in physical properties.
本発明において、「非流動性」とは、少なくとも液状ではなく、無負荷の状態で実質的に変形・流動しないことを意味し、好適には、25℃かつ無負荷の状態で変形・流動しないことを意味する。このような反応物は、好適には、コーン・プレートまたはパラレル・プレート式の動的粘弾性測定装置を用いて振動数1ヘルツで測定される貯蔵弾性率(G’)が1000Pa以上である。なお、非流動性を有する反応物においては、増粘乃至硬化が進行した結果、ゲル状乃至固体状(弾性体および熱可塑体を含む)の反応物を形成しており、当該反応物の粘度測定が実質的に困難であることが好ましい。なお、本発明において、反応物は非流動性であれば、少なくとも一段階以上の硬化反応が実質的に完結していなくてもよく、表面の増粘乃至硬化により流動性を失っていれば、その深部において硬化反応が進行していなくてもよい。反応物が非流動性であれば、本発明の主要な技術的効果の一つである表示装置の目張りが達成されるためである。 In the present invention, “non-flowable” means that it is not at least liquid and does not substantially deform or flow in an unloaded state, and preferably does not deform or flow in an unloaded state at 25 ° C. Means that. Such a reactant preferably has a storage elastic modulus (G ′) of 1000 Pa or more measured at a frequency of 1 hertz using a cone plate or parallel plate type dynamic viscoelasticity measuring apparatus. In addition, in the reactant having non-fluidity, as a result of the progress of thickening or curing, a gel-like or solid (including elastic body and thermoplastic) reactant is formed, and the viscosity of the reactant It is preferable that the measurement is substantially difficult. In the present invention, if the reactant is non-flowable, at least one stage of curing reaction may not be substantially completed, and if the fluidity is lost due to surface thickening or curing, The curing reaction does not have to proceed in the deep part. This is because, if the reactant is non-fluid, the scale of the display device, which is one of the main technical effects of the present invention, is achieved.
本発明において、「初期粘度」とは、各成分の混合により、組成物を調製した直後における組成物全体の混合粘度であり、レオメーター等を用いて測定可能である。すなわち、本発明にかかる表示装置用のギャップシール剤組成物は、各成分を、その使用前に混合して調製される多成分型(特に、2成分型を含む)の組成物であることが好ましく、多成分の混合直後において、液状かつ一定の粘度範囲にあるので、表示装置の空隙に注入可能である。 In the present invention, the “initial viscosity” is a mixed viscosity of the entire composition immediately after the composition is prepared by mixing each component, and can be measured using a rheometer or the like. That is, the gap sealant composition for a display device according to the present invention is a multi-component type composition (particularly including a two-component type) prepared by mixing each component before use. Preferably, immediately after mixing of the multi-components, it is liquid and in a certain viscosity range, so that it can be injected into the gap of the display device.
本発明の表示装置用のギャップシール剤組成物は、(A)分子内に硬化反応性官能基を有する、1種類以上のオルガノポリシロキサン、
および
(B)硬化反応触媒
を含有してなり、25℃における初期粘度が100~100000mPa・s の範囲の液状であり、さらに、同温度下で少なくとも30分以内に非流動性の反応物を形成することを特徴とする。
The gap sealant composition for a display device of the present invention comprises (A) one or more types of organopolysiloxane having a curing reactive functional group in the molecule,
And (B) a liquid containing a curing reaction catalyst and having an initial viscosity at 25 ° C. in the range of 100 to 100,000 mPa · s, and forming a non-flowable reactant within at least 30 minutes at the same temperature. It is characterized by doing.
本発明の組成物は、その硬化プロファイルに特徴を有する。すなわち、各成分を混合した直後においては、液状かつ25℃における初期粘度が100~100000mPa・s の範囲にあるので、L字ノズル/ニードル等を備えたディスペンサーを用いて、表示装置の空隙、特に、ベゼルと表示パネルとの空隙に注入することができる一方、25℃において少なくとも30分以内に非流動性の反応物を形成し、当該空隙の目張りを実現するという速硬化性または速乾性の硬化プロファイルを有するものである。 The composition of the present invention is characterized by its curing profile. That is, immediately after mixing each component, the initial viscosity at 25 ° C. is in the range of 100 to 100000 mPa · s. Therefore, using a dispenser equipped with an L-shaped nozzle / needle, etc. Can be injected into the gap between the bezel and the display panel, while forming a non-flowable reactant at 25 ° C. within at least 30 minutes to achieve the void-clad or fast-curing curing. It has a profile.
その初期粘度は、前記範囲であれば表示装置用のギャップシール剤組成物として十分な取扱作業性を実現するものであるが、可使時間および注入後の表示モジュール側への流出防止および充填性の見地から、初期粘度が500~50000mPa・s の範囲であってよく、750~30000mPa・s の範囲がより好ましく、1000~25000mPa・s の範囲であることが実用上、特に好ましい。初期粘度が前記下限未満では、速硬化性または速乾性の硬化プロファイルにおいても、流動性が高いため、注入後の表示モジュール側への流出や、特に垂直方向への充填不良が発生する場合がある。一方、初期粘度が前記上限を超えると、注入作業中に増粘/硬化が過度に進行し、注入工程における十分な可使時間が確保できない場合がある。 If the initial viscosity is within the above range, it will realize sufficient handling workability as a gap sealant composition for a display device. From this viewpoint, the initial viscosity may be in the range of 500 to 50000 mPa · s, more preferably in the range of 750 to 30000 mPa · s, and particularly preferably in the range of 1000 to 25000 mPa · s in practice. If the initial viscosity is less than the lower limit, even in a fast-curing or quick-drying curing profile, the fluidity is high, so that there are cases where outflow to the display module side after injection or in particular poor filling in the vertical direction may occur. . On the other hand, if the initial viscosity exceeds the upper limit, thickening / curing may proceed excessively during the pouring operation, and sufficient pot life in the pouring process may not be ensured.
30分以内に非流動性の反応物を形成するとは、混合操作等で本発明にかかる組成物が調製された直後の時点を起点(=0分)として、室温で他の硬化操作(例えば、紫外線の照射や加熱、加水等の硬化操作)を行わなくても、少なくとも30分経過後には、上記の液状組成物が非流動性の反応物の状態となるまで、少なくとも一段階以上の硬化反応が進行していることを意味するものである。また、本組成物は、30分経過前(例えば、15分、20分、25分経過等)のいずれかの時点において、非流動性の反応物となっていてもよく、30分以上経過後にさらに硬化反応が進行してもよい。 Forming a non-flowable reactant within 30 minutes means that another curing operation (for example, for example, at room temperature, starting from the time immediately after the composition according to the present invention is prepared by mixing operation or the like (= 0 minutes)). At least one stage of curing reaction until the liquid composition becomes a non-flowable reactant after at least 30 minutes, without performing ultraviolet irradiation, heating, and other curing operations). Means that it is progressing. In addition, the composition may be a non-fluid reactant at any time before 30 minutes (for example, 15 minutes, 20 minutes, 25 minutes, etc.), and after 30 minutes or more. Further, the curing reaction may proceed.
本発明にかかる組成物は、さらに、混合操作等で本発明にかかる組成物が調製された直後の時点を起点(=0分)として、少なくとも30分経過後には、同組成物からなる反応物が、コーン・プレートまたはパラレル・プレート式の動的粘弾性測定装置を用いて振動数1ヘルツで測定される貯蔵弾性率(G’)が1000Pa以上となることが特に好ましい。 The composition according to the present invention is further a reaction product comprising the same composition after at least 30 minutes from the time point immediately after the composition according to the present invention is prepared by mixing operation or the like (= 0 minute). However, it is particularly preferable that the storage elastic modulus (G ′) measured at a frequency of 1 hertz using a cone plate or parallel plate type dynamic viscoelasticity measuring apparatus is 1000 Pa or more.
本発明にかかる組成物が非流動性の反応物の状態乃至上記の貯蔵弾性率(G’)が1000Pa以上の値に達するまでの時間は、後述する組成物の成分(A)、成分(B)の種類および量を適宜選択したり、組成物の硬化系に対する阻害剤(例えば、ヒドロシリル化反応を含む硬化系に対する硬化抑制剤)の種類および量を選択することで設計乃至制御することが可能である。例えば、成分(A)が室温下で成分(B)の存在下で硬化反応が進行する場合、成分(B)の量を増加させ、成分(B)に対する阻害剤を添加しない、あるいは、注入までの可使時間を確保する最小限の量とすることで、組成物の速硬化性または速乾性の硬化プロファイルが設計可能である。 The time required for the composition according to the present invention to be in the state of a non-flowable reactant or the above storage elastic modulus (G ′) to reach a value of 1000 Pa or more depends on the components (A) and (B ) Can be designed or controlled by appropriately selecting the type and amount of the composition or by selecting the type and amount of an inhibitor for the curing system of the composition (for example, a curing inhibitor for the curing system including a hydrosilylation reaction). It is. For example, when the curing reaction proceeds in the presence of component (B) at room temperature in the presence of component (A), the amount of component (B) is increased and no inhibitor for component (B) is added, or until injection By setting the minimum amount to ensure the pot life, it is possible to design a fast-curing or quick-drying curing profile of the composition.
また、本発明にかかる組成物は、前記のとおり、表示装置の空隙、特に、ベゼルと表示パネルとの空隙に注入する工程においては液状を保ち、可使時間を確保する必要がある。本発明にかかる組成物が形成されるタイミングは、例えば、組成物を2液等の多成分の形態で保管しておき、これを注入時に混合することで選択することが可能である。例えば、各成分を注入直前にミキサー等で混合して、可使時間内にディスペンサーに装填して所望の部位に注入してよい。なお、この場合、混合時が上記の非流動性の反応物を形成する硬化反応の起点(=0分)となるため、工程および注入操作時間にもよるが、混合後、少なくとも3分以内、好適には5分以内の間は、非流動性の反応物を形成しないことが好ましい。このように、室温で十分な可使時間を確保しつつ、速硬化性または速乾性の硬化プロファイルを有するような組成物を設計することで、注入時の液詰まりや吐出不良等の不具合の発生を抑制して、本発明を円滑に実施できる実益がある。 Further, as described above, the composition according to the present invention needs to maintain a liquid state and ensure a pot life in the step of injecting into the gap of the display device, particularly the gap between the bezel and the display panel. The timing at which the composition according to the present invention is formed can be selected, for example, by storing the composition in a multi-component form such as two liquids and mixing it at the time of injection. For example, each component may be mixed with a mixer or the like immediately before injection, loaded into a dispenser within the pot life, and injected into a desired site. In this case, since the time of mixing becomes the starting point (= 0 minutes) of the curing reaction that forms the above-mentioned non-flowable reactant, depending on the process and the injection operation time, at least within 3 minutes after mixing, Preferably, no non-flowable reactant is formed within 5 minutes. In this way, by designing a composition that has a fast-curing or quick-drying curing profile while ensuring sufficient pot life at room temperature, problems such as clogging during liquid injection and defective discharge occur. There is an actual advantage that the present invention can be smoothly implemented.
一方、本発明の実施にあたっては、物理的に仕切りが設けられた液状原料タンクと、吐出部に各原料タンクから供給される液状原料を一定量ずつ混合する機構を備えたディスペンサーを用いてもよい。このような、原料液を分離して装填可能なタンクの機構と混合機構を備えたディスペンサーを用いることで、本発明にかかる組成物の各成分を物理的に仕切られたタンク内に装填し、ディスペンス時に一定量ずつ混合して吐出することも可能である。この場合、吐出時と混合時のタイムラグが事実上ゼロとなるように組成物を形成して所望の部位に注入可能であるので、上記の混合後の組成物の可使時間が仮に短くても、本発明にかかる組成物および表示装置の製造方法を問題なく実施できる。すなわち、本発明にかかる組成物は、その混合手段および注入へのタイミングを選択可能なので、室温における可使時間の確保は、任意の要素である。なお、このような構造を備えたディスペンサーは市販されており、一例として、MIX-PAC社製プラスチック2連カートリッジに吐出ノズルを設けたディスペンサー等が例示できる。 On the other hand, in carrying out the present invention, a dispenser having a liquid raw material tank physically provided with a partition and a mechanism for mixing a predetermined amount of liquid raw material supplied from each raw material tank to the discharge unit may be used. . By using such a dispenser having a tank mechanism and a mixing mechanism that can separate and load the raw material liquid, each component of the composition according to the present invention is loaded into a physically partitioned tank, It is also possible to mix and discharge a certain amount at the time of dispensing. In this case, since the composition can be formed and injected into a desired site so that the time lag between discharge and mixing is virtually zero, even if the pot life of the composition after mixing is short The composition and the method for producing a display device according to the present invention can be carried out without any problem. That is, since the composition according to the present invention can select the mixing means and the timing of injection, securing the pot life at room temperature is an optional factor. A dispenser having such a structure is commercially available. For example, a dispenser in which a discharge nozzle is provided in a plastic double cartridge manufactured by MIX-PAC can be exemplified.
次に、本発明にかかる組成物は、下記の成分(A)および成分(B)を含有する。 Next, the composition concerning this invention contains the following component (A) and component (B).
成分(A)は、分子内に硬化反応性官能基を有する、1種類以上のオルガノポリシロキサンであり、以下のオルガノポリシロキサンのいずれか、またはこれらの組み合わせを含んでよい。
分子内に、1種類または2種類以上の硬化反応性官能基を有するオルガノポリシロキサン、
互いに異なる硬化反応性官能基を有する、2種類以上のオルガノポリシロキサン、
同一の硬化反応性官能基を有するが、その結合部位、含有量、およびシロキサン骨格のいずれかにおいて互いに相違する、2種類以上のオルガノポリシロキサン
Component (A) is one or more organopolysiloxanes having a curing reactive functional group in the molecule, and may include any of the following organopolysiloxanes or a combination thereof.
An organopolysiloxane having one or more kinds of curing reactive functional groups in the molecule;
Two or more types of organopolysiloxanes having different curing reactive functional groups,
Two or more types of organopolysiloxanes having the same curing reactive functional group but different from each other in any of the bonding site, content, and siloxane skeleton
成分(A)の硬化反応性官能基として、ヒドロシリル化反応性基、ラジカル反応性基、縮合反応性官能基等の任意の硬化反応性官能基が例示され、特に、炭素-炭素二重結合を有するヒドロシリル化反応性基またはラジカル反応性基;珪素原子結合水素基であるヒドロシリル化反応性基;水酸基、アルコキシ基、アシロキシ基、オキシモキシ基から選ばれる縮合反応性基が好適に例示される。なお、ラジカル反応性基は、紫外線等の高エネルギー線反応性基を含む。本発明にかかる成分(A)は、1種の硬化反応性基を分子内に含むオルガノポリシロキサンであってもよく、2種類以上の異なる硬化反応性基を分子内に含むオルガノポリシロキサンであってもよく、硬化反応性官能基の種類/結合部位/含有量/シロキサン骨格のいずれかにおいて互いに異なるオルガノポリシロキサンの混合物であってもよい。 Examples of the curing reactive functional group of component (A) include any curing reactive functional group such as a hydrosilylation reactive group, a radical reactive group, a condensation reactive functional group, and in particular, a carbon-carbon double bond. Preferred examples thereof include hydrosilylation reactive groups or radical reactive groups; hydrosilylation reactive groups that are silicon-bonded hydrogen groups; and condensation reactive groups selected from hydroxyl groups, alkoxy groups, acyloxy groups, and oximoxy groups. The radical reactive group includes a high energy ray reactive group such as ultraviolet rays. Component (A) according to the present invention may be an organopolysiloxane containing one kind of curing reactive group in the molecule, or an organopolysiloxane containing two or more different kinds of curing reactive groups in the molecule. Alternatively, it may be a mixture of organopolysiloxanes different from each other in the kind of curing reactive functional group / bonding site / content / siloxane skeleton.
本発明にかかる成分(A)として、特に好適には、
(A1)炭素-炭素二重結合を含む硬化反応性基を有するオルガノポリシロキサン、
(A2)縮合反応性基を有するオルガノポリシロキサン、および
(A3)珪素原子結合水素原子を有するオルガノハイドロジェンポリシロキサン
が例示され、成分(A1)および成分(A2)から選ばれる1種類以上のオルガノポリシロキサンを少なくとも含む組成物が、本発明において好ましい。ここで、成分(A1)を含む組成物はヒドロシリル化反応またはラジカル反応により硬化する。一方、成分(A2)を含む組成物は縮合反応により硬化する。
As the component (A) according to the present invention, particularly preferably,
(A1) an organopolysiloxane having a curing reactive group containing a carbon-carbon double bond,
(A2) Organopolysiloxane having a condensation reactive group, and (A3) organohydrogenpolysiloxane having a silicon atom-bonded hydrogen atom are exemplified, and one or more kinds of organos selected from component (A1) and component (A2) A composition containing at least polysiloxane is preferred in the present invention. Here, the composition containing the component (A1) is cured by a hydrosilylation reaction or a radical reaction. On the other hand, the composition containing the component (A2) is cured by a condensation reaction.
本発明にかかる組成物の成分(A)は、ヒドロシリル化反応硬化性であることが好ましく、上記の成分(A1)および成分(A3)を共に含むオルガノポリシロキサン混合物が好ましい。 The component (A) of the composition according to the present invention is preferably hydrosilylation reaction curable, and an organopolysiloxane mixture containing both the component (A1) and the component (A3) is preferable.
成分(A1)は、炭素-炭素二重結合を含む硬化反応性基を有するオルガノポリシロキサンであり、ビニル基、アリル基、ブテニル基、ペンテニル基、ヘキセニル基、ヘプテニル基、オクテニル基、ノネニル基、デセニル基、ウンデセニル基、ドデセニル基等の炭素数2~20のアルケニル基;3-アクリロキシプロピル基、4-アクリロキシブチル基等のアクリル含有基;3-メタクリロキシプロピル基、4-メタクリロキシブチル基等のメタクリル含有基から選ばれる硬化反応性基を分子内に含有する、直鎖状、分岐鎖状、環状、または樹脂状(ネットワーク状)のオルガノポリシロキサンが例示される。特に、ビニル基、アリル基またはヘキセニル基から選ばれる炭素-炭素二重結合を含む硬化反応性基を有するオルガノポリシロキサンが好ましい。 Component (A1) is an organopolysiloxane having a curing reactive group containing a carbon-carbon double bond, vinyl group, allyl group, butenyl group, pentenyl group, hexenyl group, heptenyl group, octenyl group, nonenyl group, C2-C20 alkenyl group such as decenyl group, undecenyl group, dodecenyl group; acrylic-containing group such as 3-acryloxypropyl group, 4-acryloxybutyl group; 3-methacryloxypropyl group, 4-methacryloxybutyl Examples thereof include linear, branched, cyclic, or resinous (network-like) organopolysiloxanes containing a curing reactive group selected from methacryl-containing groups such as groups in the molecule. In particular, an organopolysiloxane having a curing reactive group containing a carbon-carbon double bond selected from a vinyl group, an allyl group or a hexenyl group is preferred.
成分(A1)であるオルガノポリシロキサンは、分子内に炭素-炭素二重結合を有しない一価炭化水素基、水酸基およびアルコキシ基から選ばれる基を含んでもよい。また、一価炭化水素基は、その水素原子の一部がハロゲン原子または水酸基で置換されていてもよい。このような一価炭化水素基の例としては、メチル基、エチル基、プロピル基、ブチル基、ペンチル基、ヘキシル基、ヘプチル基、オクチル基、ノニル基、デシル基、ウンデシル基、ドデシル基などのアルキル基;フェニル基、トリル基、キシリル基、ナフチル基、アントラセニル基、フェナントリル基、ピレニル基などのアリール基;ベンジル基、フェネチル基、ナフチルエチル基、ナフチルプロピル基、アントラセニルエチル基、フェナントリルエチル基、ピレニルエチル基などのアラルキル基;およびこれらのアリール基またはアラルキル基の水素原子をメチル基、エチル基等のアルキル基;メトキシ基、エトキシ基等のアルコキシ基;塩素原子、臭素原子等のハロゲン原子で置換した基が挙げられる。なお、成分(A1)が、水酸基等を含む場合、当該成分は、ヒドロシリル化反応硬化性に加えて、縮合反応性を有する。 The organopolysiloxane as the component (A1) may contain a group selected from a monovalent hydrocarbon group, a hydroxyl group and an alkoxy group having no carbon-carbon double bond in the molecule. Moreover, in the monovalent hydrocarbon group, a part of the hydrogen atoms may be substituted with a halogen atom or a hydroxyl group. Examples of such monovalent hydrocarbon groups include methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and the like. Alkyl group; phenyl group, tolyl group, xylyl group, naphthyl group, anthracenyl group, phenanthryl group, pyrenyl group and other aryl groups; benzyl group, phenethyl group, naphthylethyl group, naphthylpropyl group, anthracenylethyl group, phenane An aralkyl group such as a tolylethyl group or a pyrenylethyl group; and a hydrogen atom of these aryl groups or aralkyl groups; an alkyl group such as a methyl group or an ethyl group; an alkoxy group such as a methoxy group or an ethoxy group; a chlorine atom or a bromine atom; And a group substituted with a halogen atom. In addition, when a component (A1) contains a hydroxyl group etc., the said component has condensation reactivity in addition to hydrosilylation reaction curability.
好適には、成分(A1)は、下記の平均組成式:
R1
aR2
bSiO(4-a―b)/2
で表されるオルガノポリシロキサン、またはその混合物であってよい。
式中、R1は、上記の炭素-炭素二重結合を含む硬化反応性基であり、
R2は、上記の炭素-炭素二重結合を有しない一価炭化水素基、水酸基およびアルコキシ基から選ばれる基であり、
aおよびbは次の条件:1≦a+b≦3及び0.001≦a/(a+b)≦0.33を満たす数であり、好ましくは、次の条件:1.5≦a+b≦2.5及び0.005≦a/(a+b)≦0.2を満たす数である。これは、a+bが上記範囲の下限以上であると、硬化物の柔軟性が高くなるからであり、一方上記範囲の上限以下であると、硬化物の機械強度が高くなるからであり、a/(a+b)が上記範囲の下限以上であると、硬化物の機械強度が高くなるからであり、一方上記範囲の上限以下であると、硬化物の柔軟性が高くなるからである。
Preferably, component (A1) has the following average composition formula:
R 1 a R 2 b SiO (4-ab) / 2
Or a mixture thereof.
Wherein R 1 is a curing reactive group containing the above carbon-carbon double bond,
R 2 is a group selected from a monovalent hydrocarbon group having no carbon-carbon double bond, a hydroxyl group and an alkoxy group,
a and b are numbers satisfying the following conditions: 1 ≦ a + b ≦ 3 and 0.001 ≦ a / (a + b) ≦ 0.33, preferably, the following conditions: 1.5 ≦ a + b ≦ 2.5 and It is a number that satisfies 0.005 ≦ a / (a + b) ≦ 0.2. This is because the flexibility of the cured product is increased when a + b is not less than the lower limit of the above range, and the mechanical strength of the cured product is increased when it is not more than the upper limit of the above range. This is because when (a + b) is equal to or higher than the lower limit of the above range, the mechanical strength of the cured product is increased, and when it is equal to or lower than the upper limit of the above range, the flexibility of the cured product is increased.
本発明にかかる組成物において、特に好適には、成分(A1)は、
成分(A1)は、
(A1-1)分子鎖末端のみにアルケニル基を有する直鎖状または分岐鎖状のオルガノポリシロキサン、および、任意で
(A1-2)分子内に少なくとも1つの分岐シロキサン単位を有し、ビニル(CH2=CH―)基の含有量が1.0~5.0質量%の範囲内にあるアルケニル基含有オルガノポリシロキサン樹脂
を含むものである。
In the composition according to the present invention, particularly preferably, the component (A1) is
Component (A1) is
(A1-1) a linear or branched organopolysiloxane having an alkenyl group only at the molecular chain end, and (A1-2) optionally having at least one branched siloxane unit in the molecule, An alkenyl group-containing organopolysiloxane resin having a CH2 = CH-) group content in the range of 1.0 to 5.0% by mass is included.
成分(A1-1)は、その分子鎖末端に
(Alk)R2
2SiO1/2
(式中、Alkは炭素原子数2以上のアルケニル基)で表されるシロキサン単位を有し、その他のシロキサン単位が実質的にR2
2SiO2/2で表されるシロキサン単位のみからなる直鎖状または分岐鎖状のオルガノポリシロキサンである。なお、R2は前記同様の基を表す。また、成分(A1-1)のシロキサン重合度は、末端シロキサン単位を含めて、7~1002の範囲である。このような成分(A1-1)は特に好適には、分子鎖の両末端が(Alk)R2
2SiO1/2で表されるシロキサン単位で封鎖された、直鎖状のオルガノポリシロキサンである。
Component (A1-1) has (Alk) R 2 2 SiO 1/2 at the molecular chain end.
(Wherein Alk is an alkenyl group having 2 or more carbon atoms), and the other siloxane units are substantially composed only of siloxane units represented by R 2 2 SiO 2/2. It is a linear or branched organopolysiloxane. R 2 represents the same group as described above. Further, the degree of siloxane polymerization of the component (A1-1) is in the range of 7 to 1002, including the terminal siloxane unit. Such component (A1-1) is particularly preferably a linear organopolysiloxane in which both ends of the molecular chain are blocked with siloxane units represented by (Alk) R 2 2 SiO 1/2. is there.
成分(A1-2)は、アルケニル基含有オルガノポリシロキサン樹脂であり、
平均単位式:
(RSiO3/2)o(R2SiO2/2)p(R3SiO1/2)q(SiO4/2)r(XO1/2)s
で表されるアルケニル基含有オルガノポリシロキサン樹脂が例示される。
上式中、Rは、アルケニル基および前記の炭素-炭素二重結合を有しない一価炭化水素基から選ばれる基であり、Xは水素原子または炭素原子数1~3のアルキル基である。ただし、全てのRのうち、少なくとも、当該オルガノポリシロキサン樹脂中のビニル(CH2=CH―)基の含有量が、1.0~5.0質量%の範囲を満たす範囲においてRはアルケニル基であり、特に、RSiO1/2で表されるシロキサン単位上のRの少なくとも一部はアルケニル基であることが好ましい。
Component (A1-2) is an alkenyl group-containing organopolysiloxane resin,
Average unit formula:
(RSIO 3/2 ) o (R 2 SiO 2/2 ) p (R 3 SiO 1/2 ) q (SiO 4/2 ) r (XO 1/2 ) s
The alkenyl group containing organopolysiloxane resin represented by these is illustrated.
In the above formula, R is a group selected from an alkenyl group and the monovalent hydrocarbon group having no carbon-carbon double bond, and X is a hydrogen atom or an alkyl group having 1 to 3 carbon atoms. However, among all R, R is an alkenyl group in a range where the content of vinyl (CH2═CH—) group in the organopolysiloxane resin satisfies the range of 1.0 to 5.0% by mass. In particular, at least a part of R on the siloxane unit represented by RSiO 1/2 is preferably an alkenyl group.
式中、(o+r)は正数であり、pは0又は正数であり、qは0又は正数であり、sは0又は正数であり、かつ、p/(o+r)は0~10の範囲内の数であり、q/(o+r)は0~5の範囲内の数であり、(o+r)/(o+p+q+r)は0.3~0.9の範囲内の数であり、s/(o+p+q+r)は0~0.4の範囲内の数である。 Where (o + r) is a positive number, p is 0 or a positive number, q is 0 or a positive number, s is 0 or a positive number, and p / (o + r) is 0 to 10 Q / (o + r) is a number in the range 0-5, (o + r) / (o + p + q + r) is a number in the range 0.3-0.9, and s / (o + p + q + r) is a number in the range of 0 to 0.4.
成分(A1-2)として、特に好適には、
{(Alk)R2
2SiO1/2}q1(R2
3SiO1/2)q2(SiO4/2)r
(式中、Alk、R2は前記同様の基であり、q1+q2+rは50~500の範囲の数であり、(q1+q2)/rは0.1~2.0の範囲の数であり、q2は当該オルガノポリシロキサン樹脂中のビニル(CH2=CH―)基の含有量が、1.0~5.0質量%の範囲を満たす範囲の数である)
で表されるアルケニル基含有MQオルガノポリシロキサン樹脂が例示される。
As component (A1-2), particularly preferably,
{(Alk) R 2 2 SiO 1/2 } q1 (R 2 3 SiO 1/2 ) q2 (SiO 4/2 ) r
(Wherein Alk and R 2 are the same groups as described above, q1 + q2 + r is a number in the range of 50 to 500, (q1 + q2) / r is a number in the range of 0.1 to 2.0, and q2 is (The number of vinyl (CH2 = CH-) groups in the organopolysiloxane resin is in a range satisfying the range of 1.0 to 5.0% by mass)
The alkenyl group containing MQ organopolysiloxane resin represented by these is illustrated.
これらの分子鎖末端のみにアルケニル基を有する成分(A1-1)およびオルガノポリシロキサン樹脂であって一定量のアルケニル基を有する成分(A1-2)を併用することで、組成物全体として速硬化性/速乾性に優れ、かつ、機械的強度および柔軟性に優れる硬化反応物を与え、表示装置におけるギャップシール用途に特に適合した表示装置用のギャップシール剤組成物を提供することができる。 By using together the component (A1-1) having an alkenyl group only at the molecular chain terminal and the component (A1-2) which is an organopolysiloxane resin having a certain amount of alkenyl group, the composition as a whole can be cured quickly. It is possible to provide a gap sealant composition for a display device that is excellent in properties / fast drying properties, gives a cured reaction product excellent in mechanical strength and flexibility, and is particularly suitable for gap seal applications in display devices.
成分(A3)は、珪素原子結合水素原子を有するオルガノハイドロジェンポリシロキサンであり、好適には、分子内に少なくとも2つの珪素原子結合水素原子を有し、成分(A1)の架橋剤として機能する成分である。 Component (A3) is an organohydrogenpolysiloxane having silicon-bonded hydrogen atoms, and preferably has at least two silicon-bonded hydrogen atoms in the molecule and functions as a crosslinking agent for component (A1). It is an ingredient.
このような成分(A3)として、1,1,3,3-テトラメチルジシロキサン、1,3,5,7-テトラメチルシクロテトラシロキサン、トリス(ジメチルハイドロジェンシロキシ)メチルシラン、トリス(ジメチルハイドロジェンシロキシ)フェニルシラン、分子鎖両末端トリメチルシロキシ基封鎖メチルハイドロジェンポリシロキサン、分子鎖両末端トリメチルシロキシ基封鎖ジメチルシロキサン・メチルハイドロジェンシロキサン共重合体、分子鎖両末端ジメチルハイドロジェンシロキシ基封鎖ジメチルポリシロキサン、分子鎖両末端ジメチルハイドロジェンシロキシ基封鎖ジメチルシロキサン・メチルハイドロジェンシロキサン共重合体、分子鎖両末端トリメチルシロキシ基封鎖メチルハイドロジェンシロキサン・ジフェニルシロキサン共重合体、分子鎖両末端トリメチルシロキシ基封鎖メチルハイドロジェンシロキサン・ジフェニルシロキサン・ジメチルシロキサン共重合体、トリメトキシシランの加水分解縮合物、(CH3)2HSiO1/2単位とSiO4/2単位とからなる共重合体、(CH3)2HSiO1/2単位とSiO4/2単位と(C6H5)SiO3/2単位とからなる共重合体、およびこれらの2種以上の混合物が例示される。 As such component (A3), 1,1,3,3-tetramethyldisiloxane, 1,3,5,7-tetramethylcyclotetrasiloxane, tris (dimethylhydrogensiloxy) methylsilane, tris (dimethylhydrogen) Siloxy) phenylsilane, trimethylsiloxy group-capped methylhydrogen polysiloxane with molecular chain at both ends, trimethylsiloxy group-capped dimethylsiloxane / methylhydrogensiloxane copolymer with molecular chain at both ends, dimethylhydrogensiloxy group-capped dimethylpoly with molecular chain at both ends Siloxane, molecular chain both ends dimethylhydrogensiloxy group-blocked dimethylsiloxane / methylhydrogensiloxane copolymer, molecular chain both ends trimethylsiloxy group-blocked methylhydrogensiloxane / diphenylsiloxane copolymer, It consists of a trimethylsiloxy group-blocked methylhydrogensiloxane / diphenylsiloxane / dimethylsiloxane copolymer, hydrolyzed condensate of trimethoxysilane, (CH 3 ) 2 HSiO 1/2 unit and SiO 4/2 unit. Examples include copolymers, copolymers composed of (CH 3 ) 2 HSiO 1/2 units, SiO 4/2 units, and (C 6 H 5 ) SiO 3/2 units, and mixtures of two or more thereof. The
本発明にかかる組成物において、特に好適には、成分(A3)は、
(A3-1)分子鎖末端のみに珪素結合水素原子を有する直鎖状または分岐鎖状のオルガノハイドロジェンポリシロキサン、および、任意で
(A3-2)分子内に少なくとも3個の珪素結合水素原子を有する直鎖状または樹脂状のオルガノハイドロジェンポリシロキサン
を含むものである。
In the composition according to the present invention, particularly preferably, the component (A3) is
(A3-1) a linear or branched organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the molecular chain end, and optionally (A3-2) at least three silicon-bonded hydrogen atoms in the molecule A linear or resinous organohydrogenpolysiloxane having the following formula is included.
成分(A3-1)は分子鎖末端のみに珪素結合水素原子を有するオルガノハイドロジェンポリシロキサンであり、前記の成分(A1)とのヒドロシリル化反応において、鎖長延長剤として機能し、硬化反応物の柔軟性を改善する成分である。このような成分(A3-1)は、好適には直鎖状のオルガノハイドロジェンポリシロキサンであり、以下の構造式で表されるものが好適に使用できる。
HMe2SiO(Ph2SiO)m1SiMe2H
HMe2SiO(Me2SiO)m1SiMe2H
HMePhSiO(Ph2SiO)m1SiMePhH
HMePhSiO(Me2SiO)m1SiMePhH
HMePhSiO(Ph2SiO)m1(MePhSiO)n1SiMePhH
HMePhSiO(Ph2SiO)m1(Me2SiO)n1SiMePhH
上式中、Me、Phは、それぞれ、メチル基、フェニル基を示し、m1は1~100の数であり、n1は1~50の数である。
Component (A3-1) is an organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the molecular chain end, and functions as a chain extender in the hydrosilylation reaction with component (A1), and is a cured reaction product. It is a component that improves the flexibility. Such component (A3-1) is preferably a linear organohydrogenpolysiloxane, and those represented by the following structural formula can be preferably used.
HMe 2 SiO (Ph 2 SiO) m1 SiMe 2 H
HMe 2 SiO (Me 2 SiO) m1 SiMe 2 H
HMePhSiO (Ph 2 SiO) m1 SiMePhH
HMePhSiO (Me 2 SiO) m1 SiMePhH
HMePhSiO (Ph 2 SiO) m1 (MePhSiO) n1 SiMePhH
HMePhSiO (Ph 2 SiO) m1 (Me 2 SiO) n1 SiMePhH
In the above formula, Me and Ph represent a methyl group and a phenyl group, respectively, m1 is a number from 1 to 100, and n1 is a number from 1 to 50.
成分(A3-2)は、分子内に少なくとも3個の珪素結合水素原子を有する直鎖状または樹脂状のオルガノハイドロジェンポリシロキサンであり、上記の成分(A3-1)と併用することで、本組成物に迅速な硬化性を実現する成分である。 Component (A3-2) is a linear or resinous organohydrogenpolysiloxane having at least three silicon-bonded hydrogen atoms in the molecule. When used in combination with component (A3-1) above, It is a component that realizes rapid curability in the composition.
直鎖状のオルガノハイドロジェンポリシロキサンとして、分子鎖両末端トリメチルシロキシ基封鎖メチルハイドロジェンポリシロキサン、分子鎖両末端トリメチルシロキシ基封鎖ジメチルシロキサン・メチルハイドロジェンシロキサン共重合体、分子鎖両末端ジメチルハイドロジェンシロキシ基封鎖ジメチルシロキサン・メチルハイドロジェンシロキサン共重合体、分子鎖両末端トリメチルシロキシ基封鎖メチルハイドロジェンシロキサン・ジフェニルシロキサン共重合体、分子鎖両末端トリメチルシロキシ基封鎖メチルハイドロジェンシロキサン・ジフェニルシロキサン・ジメチルシロキサン共重合体が例示される。 As linear organohydrogenpolysiloxanes, trimethylsiloxy group-capped methylhydrogen polysiloxanes at both molecular chain ends, trimethylsiloxy group-capped dimethylsiloxane / methylhydrogensiloxane copolymers with both molecular chain terminals, and dimethylhydrol at both molecular chain terminals. Gensiloxy group-blocked dimethylsiloxane / methylhydrogensiloxane copolymer, molecular chain both ends trimethylsiloxy group-blocked methylhydrogensiloxane / diphenylsiloxane copolymer, molecular chain both ends trimethylsiloxy group-blocked methylhydrogensiloxane / diphenylsiloxane, A dimethylsiloxane copolymer is exemplified.
他方、樹脂状のオルガノハイドロジェンポリシロキサンとして、少なくともSiO4/2単位(Q単位)およびR3SiO3/2単位(T単位)から選ばれる分岐シロキサン単位を含んでなり、R3
3SiO1/2単位(M単位)、R3
2HSiO1/2単位(MH単位)、および任意でR3
2SiO1/2単位(D単位)、R3HSiO1/2単位(DH単位)を含んで成る、
MHMQ型、MHQ型、MHMT型、MHT型、MHMQT型、MHQT型、MHMDQ型、MHMDDHQ型、MHDQ型、MHDDHQ型、MHMDT型、MHMDDHT型、MHDT型、MHDDHT型、MHMDQT型、MHMDDHQT型、MHDQT型、MHDDHQT型から選ばれる1種類以上のオルガノハイドロジェンポリシロキサン樹脂が例示される。
なお、式中、R3はメチル基またはフェニル基である。
On the other hand, the resinous organohydrogenpolysiloxane comprises at least a branched siloxane unit selected from an SiO 4/2 unit (Q unit) and an R 3 SiO 3/2 unit (T unit), and R 3 3 SiO 1 / 2 units (M units), R 3 2 HSiO 1/2 units ( MH units), and optionally R 3 2 SiO 1/2 units (D units), R 3 HSiO 1/2 units ( DH units) Comprising
M H MQ type, M H Q type, M H MT type, M H T type, M H MQT type, M H QT type, M H MDQ type, M H MDD H Q type, M H DQ type, M H DD H Q type, MH MDT type, MH MDD H T type, MH DT type, MH DD H T type, MH MDQT type, MH MDD H QT type, MH DQT type, MH DD H QT One or more types of organohydrogenpolysiloxane resins selected from molds are exemplified.
In the formula, R 3 is a methyl group or a phenyl group.
本発明にかかる組成物において、成分(A3)の含有量は、組成物中の、好適には、成分(A1)中の炭素-炭素二重結合1モルに対して、珪素結合水素原子が0.1~10モルの範囲となる量であり、好適には、0.2~5.0モルの範囲となる量であり、特に好適には、0.5~2.0モルの範囲となる量である。成分(A3)の含有量が前記下限以下では硬化不良の原因となる場合があり、成分(A3)の含有量が前記上限を超えると、硬化物の機械的強度が高くなりすぎ、弾性体またはゲル状の硬化反応物を得られなくなる場合がある。 In the composition according to the present invention, the content of component (A3) is preferably such that the number of silicon-bonded hydrogen atoms in the composition is preferably 0 with respect to 1 mole of carbon-carbon double bonds in component (A1). The amount is in the range of 1 to 10 mol, preferably in the range of 0.2 to 5.0 mol, particularly preferably in the range of 0.5 to 2.0 mol. Amount. If the content of the component (A3) is below the lower limit, it may cause poor curing. If the content of the component (A3) exceeds the upper limit, the mechanical strength of the cured product becomes too high, and the elastic body or A gel-like cured reaction product may not be obtained.
本発明にかかる組成物において、表示装置におけるギャップシール性、特に、速硬化性/速乾性と硬化物の正常のバランスの見地から、特に好適には、成分(A)が、
上記の成分(A1-1)100質量部および上記の成分(A1-2)0~20質量部を含む成分(A1)に対して、
上記の成分(A3-1) 成分(A1-1)および(A1-2)中のビニル基の合計1モルに対して珪素結合水素原子が0.1~10モルとなる量、好適には、0.2~5.0モルとなる量、より好適には、0.5~2.0モルとなる量、および
上記の成分(A3-2) 成分(A1-1)および(A1-2)中のビニル基の合計1モルに対して珪素結合水素原子が0~1モルとなる量、好適には、0~0.5モルとなる量、より好適には、0.1~0.5モルとなる量
のオルガノポリシロキサンを含有するものである。
In the composition according to the present invention, the gap sealability in the display device, in particular, from the viewpoint of the normal balance between the fast curing / fast drying property and the cured product, the component (A) is particularly preferably
With respect to component (A1) containing 100 parts by weight of the above component (A1-1) and 0 to 20 parts by weight of the above component (A1-2),
Component (A3-1) An amount such that silicon-bonded hydrogen atoms are 0.1 to 10 moles relative to a total of 1 mole of vinyl groups in components (A1-1) and (A1-2), preferably An amount of 0.2 to 5.0 mol, more preferably an amount of 0.5 to 2.0 mol, and the above component (A3-2) components (A1-1) and (A1-2) The amount of silicon-bonded hydrogen atoms is 0 to 1 mol, preferably 0 to 0.5 mol, more preferably 0.1 to 0.5 mol with respect to 1 mol of the total vinyl groups therein. It contains an organopolysiloxane in a molar amount.
本発明にかかる組成物において、成分(A)は、(A2)縮合反応性基を有するオルガノポリシロキサンであってもよく、特に、上記の水酸基、アルコキシ基、アシロキシ基、オキシモキシ基から選ばれる縮合反応性基を分子鎖末端のみに有する1種類または2種類以上のオルガノポリシロキサンを含有するオルガノポリシロキサン(A2-1)であってよい。かかる縮合反応性の成分(A2)は、上記の成分(A1)等のヒドロシリル化反応性のオルガノポリシロキサンと併用してもよく、後述する(B)硬化剤として、多量の縮合反応触媒を使用する等の組成設計により、成分(A2)のみで、本発明に必要な速硬化性/速乾性の硬化プロファイルを設計してもよい。 In the composition according to the present invention, the component (A) may be (A2) an organopolysiloxane having a condensation reactive group, and in particular, a condensation selected from the above hydroxyl group, alkoxy group, acyloxy group, and oximoxy group. It may be an organopolysiloxane (A2-1) containing one or more types of organopolysiloxane having a reactive group only at the molecular chain end. Such a condensation-reactive component (A2) may be used in combination with a hydrosilylation-reactive organopolysiloxane such as the above-mentioned component (A1), and a large amount of condensation reaction catalyst is used as the curing agent (B) described later. By the composition design such as, the quick curing / quick drying curing profile necessary for the present invention may be designed only by the component (A2).
成分(B)は、硬化反応触媒であり、成分(A)の硬化反応性官能基に対して硬化反応を進行させる成分である。このような成分(B)として、ヒドロシリル化反応触媒、光重合開始剤、過酸化物、または縮合反応触媒が例示されるが、表示装置用のギャップシール剤組成物として使用する都合上、加熱または大量の高エネルギー線照射が困難であることが多いため、ヒドロシリル化反応触媒または縮合反応触媒を含むことが好ましい。 Component (B) is a curing reaction catalyst, and is a component that causes the curing reaction to proceed with respect to the curing reactive functional group of component (A). Examples of such component (B) include a hydrosilylation reaction catalyst, a photopolymerization initiator, a peroxide, or a condensation reaction catalyst. For convenience of use as a gap sealant composition for a display device, Since it is often difficult to irradiate a large amount of high energy rays, it is preferable to include a hydrosilylation reaction catalyst or a condensation reaction catalyst.
(B1)ヒドロシリル化反応触媒は、成分(A)が、上記の成分(A1)、好適には上記の成分(A1)および成分(A2)を共に含み、ヒドロシリル化反応により硬化する硬化反応性官能基を有する場合に硬化反応を進行させる成分であり、特に、本発明の用途においては、
(B1-1)高エネルギー線の照射なしで、組成物中で活性を示す第一のヒドロシリル化反応触媒、及び、任意で
(B1-2)高エネルギー線の照射がないと活性を示さないが、高エネルギー線の照射により組成物中で活性を示す第二のヒドロシリル化反応触媒
を含む硬化反応触媒であって、(B1-1)成分と(B1-2)成分の質量比が100/0~5/95の範囲であるものが好ましい。
(B1) In the hydrosilylation reaction catalyst, the component (A) includes the component (A1), preferably both the component (A1) and the component (A2), and is cured by a hydrosilylation reaction. In the case of having a group, it is a component that causes a curing reaction to proceed.
(B1-1) a first hydrosilylation reaction catalyst that shows activity in the composition without irradiation with high energy rays, and optionally (B1-2) shows no activity without irradiation with high energy rays. A curing reaction catalyst comprising a second hydrosilylation reaction catalyst that is active in the composition by irradiation with high energy rays, wherein the mass ratio of the component (B1-1) to the component (B1-2) is 100/0 Those in the range of ~ 5/95 are preferred.
ここで、高エネルギー線は、紫外線、X線および電子線が挙げられ、これらのうちでも紫外線が触媒活性化の効率の点から好ましい。また、照射量は、高エネルギー線活性型触媒の種類により異なるが、紫外線の場合は、波長365nmでの積算照射量が100mJ/cm2~10J/cm2の範囲内であることが好ましい。
Here, examples of the high energy rays include ultraviolet rays, X-rays, and electron beams. Among these, ultraviolet rays are preferable from the viewpoint of efficiency of catalyst activation. The irradiation amount varies depending on the type of the high energy ray active catalyst, but in the case of ultraviolet rays, the integrated irradiation amount at a wavelength of 365 nm is preferably within a range of 100 mJ /
成分(B1-1)は、高エネルギー線の照射なしで、本組成物中で活性を示す第一のヒドロシリル化触媒である。当該成分は、ヒドロシリル化反応抑制剤を含まない、あるいは、少量である場合に、本組成物に必要な速硬化性/速乾性の硬化プロファイルを与えるヒドロシリル化反応用触媒であり、白金系触媒、ロジウム系触媒、パラジウム系触媒、ニッケル系触媒、イリジウム系触媒、ルテニウム系触媒、および鉄系触媒が例示され、好ましくは、白金系触媒である。この白金系触媒としては、白金微粉末、白金黒、白金担持シリカ微粉末、白金担持活性炭、塩化白金酸、塩化白金酸のアルコール溶液、白金のオレフィン錯体、白金のアルケニルシロキサン錯体等の白金系化合物が例示され、特に白金のアルケニルシロキサン錯体が好ましい。このアルケニルシロキサンとしては、1,3-ジビニル-1,1,3,3-テトラメチルジシロキサン、1,3,5,7-テトラメチル-1,3,5,7-テトラビニルシクロテトラシロキサン、これらのアルケニルシロキサンのメチル基の一部をエチル基、フェニル基等で置換したアルケニルシロキサン、これらのアルケニルシロキサンのビニル基をアリル基、ヘキセニル基等で置換したアルケニルシロキサンが例示される。特に、この白金-アルケニルシロキサン錯体の安定性が良好であることから、1,3-ジビニル-1,1,3,3-テトラメチルジシロキサンが好ましい。また、この白金-アルケニルシロキサン錯体の安定性を向上させることができることから、この錯体に1,3-ジビニル-1,1,3,3-テトラメチルジシロキサン、1,3-ジアリル-1,1,3,3-テトラメチルジシロキサン、1,3-ジビニル-1,3-ジメチル-1,3-ジフェニルジシロキサン、1,3-ジビニル-1,1,3,3-テトラフェニルジシロキサン、1,3,5,7-テトラメチル-1,3,5,7-テトラビニルシクロテトラシロキサン等のアルケニルシロキサンやジメチルシロキサンオリゴマー等のオルガノシロキサンオリゴマーを添加することが好ましく、特に、アルケニルシロキサンを添加することが好ましい。 Component (B1-1) is the first hydrosilylation catalyst that shows activity in the present composition without irradiation with high energy rays. The component is a hydrosilylation reaction catalyst that gives a fast curing / fast drying curing profile necessary for the composition when it contains no hydrosilylation reaction inhibitor or in a small amount. Examples include rhodium-based catalysts, palladium-based catalysts, nickel-based catalysts, iridium-based catalysts, ruthenium-based catalysts, and iron-based catalysts, and platinum-based catalysts are preferred. Platinum-based compounds such as platinum fine powder, platinum black, platinum-supported silica fine powder, platinum-supported activated carbon, chloroplatinic acid, chloroplatinic acid alcohol solution, platinum olefin complex, platinum alkenylsiloxane complex, etc. In particular, platinum alkenylsiloxane complexes are preferred. Examples of the alkenylsiloxane include 1,3-divinyl-1,1,3,3-tetramethyldisiloxane, 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane, Examples thereof include alkenyl siloxanes in which part of the methyl groups of these alkenyl siloxanes are substituted with ethyl groups, phenyl groups, and the like, and alkenyl siloxanes in which the vinyl groups of these alkenyl siloxanes are substituted with allyl groups, hexenyl groups, and the like. In particular, 1,3-divinyl-1,1,3,3-tetramethyldisiloxane is preferred because the stability of this platinum-alkenylsiloxane complex is good. Further, since the stability of the platinum-alkenylsiloxane complex can be improved, 1,3-divinyl-1,1,3,3-tetramethyldisiloxane and 1,3-diallyl-1,1 are added to this complex. , 3,3-tetramethyldisiloxane, 1,3-divinyl-1,3-dimethyl-1,3-diphenyldisiloxane, 1,3-divinyl-1,1,3,3-tetraphenyldisiloxane, It is preferable to add an alkenyl siloxane such as 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane or an organosiloxane oligomer such as a dimethylsiloxane oligomer. It is preferable.
成分(B1-1)は、高エネルギー線の照射なしで活性を示す触媒であるが、その中でも比較的低温でも活性を示すものが好ましい。具体的には、0~200℃の温度範囲において組成物中で活性を示し、ヒドロシリル化反応を促進する。成分(B1-1)の含有量は、触媒の種類及び組成物の種類によって異なるが、通常は組成物に対して、この触媒中の金属原子が質量単位で0.01~50ppmの範囲内となる量であり、特に(B1-1-1)白金のアルケニルシロキサン錯体を用いて、白金含有量が好ましくは1.5~30ppmの範囲内となる量とすることが、本発明の速硬化性/速乾性の見地からは特に好ましい。成分(B1-1)の添加量が少なすぎると、速硬化性という本発明の目的を達成できず、添加量が多すぎると、可使時間が短すぎて実用上の不都合を生じるほか、不経済である。 Component (B1-1) is a catalyst that shows activity without irradiation with high energy rays, and among them, a catalyst that shows activity even at a relatively low temperature is preferable. Specifically, it exhibits activity in the composition in the temperature range of 0 to 200 ° C., and accelerates the hydrosilylation reaction. The content of component (B1-1) varies depending on the type of catalyst and the type of composition, but usually the metal atoms in the catalyst are within the range of 0.01 to 50 ppm by mass relative to the composition. In particular, the (B1-1-1) platinum alkenylsiloxane complex is used so that the platinum content is preferably in the range of 1.5 to 30 ppm. / It is particularly preferable from the viewpoint of quick drying. If the amount of component (B1-1) added is too small, the object of the present invention of fast curability cannot be achieved. If the amount added is too large, the pot life is too short, resulting in practical inconveniences. It is an economy.
成分(B1-2)は、高エネルギー線の照射がないと活性を示さないが、高エネルギー線の照射により本組成物中で活性を示す第二のヒドロシリル化触媒であり、いわゆる高エネルギー線活性化触媒または光活性化触媒と呼ばれるものである。 Component (B1-2) is a second hydrosilylation catalyst that exhibits activity in the present composition when irradiated with high energy rays, but does not exhibit activity without irradiation with high energy rays. The so-called activating catalyst or photoactivated catalyst.
成分(B1-2)の具体例としては、(メチルシクロペンタジエニル)トリメチル白金(IV)、(シクロペンタジエニル)トリメチル白金(IV)、(1,2,3,4,5-ペンタメチルシクロペンタジエニル)トリメチル白金(IV)、(シクロペンタジエニル)ジメチルエチル白金(IV)、(シクロペンタジエニル)ジメチルアセチル白金(IV)、(トリメチルシリルシクロペンタジエニル)トリメチル白金(IV)、(メトキシカルボニルシクロペンタジエニル)トリメチル白金(IV)、(ジメチルフェニルシリルシクロペンタジエニル)トリメチルシクロペンタジエニル白金(IV)、トリメチル(アセチルアセトナト)白金(IV)、トリメチル(3,5-ヘプタンジオネート)白金(IV)、トリメチル(メチルアセトアセテート)白金(IV)、ビス(2,4-ペンタンジオナト)白金(II)、ビス(2,4-へキサンジオナト)白金(II)、ビス(2,4-へプタンジオナト)白金(II)、ビス(3,5-ヘプタンジオナト)白金(II)、ビス(1-フェニル-1,3-ブタンジオナト)白金(II)、ビス(1,3-ジフェニル-1,3-プロパンジオナト)白金(II)、ビス(ヘキサフルオロアセチルアセトナト)白金(II)が挙げられ、これらのうちでも(メチルシクロペンタジエニル)トリメチル白金(IV)とビス(2,4-ペンタンジオナト)白金(II)が汎用性と入手の容易さの点から好ましい。 Specific examples of component (B1-2) include (methylcyclopentadienyl) trimethylplatinum (IV), (cyclopentadienyl) trimethylplatinum (IV), (1,2,3,4,5-pentamethyl (Cyclopentadienyl) trimethylplatinum (IV), (cyclopentadienyl) dimethylethylplatinum (IV), (cyclopentadienyl) dimethylacetylplatinum (IV), (trimethylsilylcyclopentadienyl) trimethylplatinum (IV), (Methoxycarbonylcyclopentadienyl) trimethylplatinum (IV), (dimethylphenylsilylcyclopentadienyl) trimethylcyclopentadienylplatinum (IV), trimethyl (acetylacetonato) platinum (IV), trimethyl (3,5- Heptanedionate) platinum (IV), trimethyl (methylacetate) Cetate) platinum (IV), bis (2,4-pentanedionato) platinum (II), bis (2,4-hexanedionato) platinum (II), bis (2,4-heptandionato) platinum (II), Bis (3,5-heptanedionato) platinum (II), bis (1-phenyl-1,3-butanedionato) platinum (II), bis (1,3-diphenyl-1,3-propanedionato) platinum (II) Bis (hexafluoroacetylacetonato) platinum (II), among which (methylcyclopentadienyl) trimethylplatinum (IV) and bis (2,4-pentanedionato) platinum (II) are widely used It is preferable from the point of property and availability.
成分(B1-2)は、本組成物において任意の成分であるが、前記の成分(B1-1)によって得た反応物に、高エネルギー線の照射により二次硬化性(以下、「光硬化性」ということがある)を付与することができるほか、前記の成分(B1-1)の存在下で同時に高エネルギー線の照射を行うことで、特にベゼル下のように十分な光照射を行えない部位においてもその硬化反応が補助的に進行し、非流動性の反応物について、さらなる硬化反応を進行させることができるほか、(B1-1)単独に比較してさらなる速硬化性/速乾性を実現できる場合がある。その含有量は、前記の成分(B1-1)によって得た反応物に組成物をさらに硬化するのに必要な量または、速硬化性/速乾性を改善するに十分な量であり、好ましくは、本組成物に対して、この触媒中の金属原子が質量単位で1~50ppmの範囲内となる量であり、好ましくは、5~30ppmの範囲内となる量である。 The component (B1-2) is an optional component in the present composition, but the reaction product obtained by the component (B1-1) is subjected to secondary curability (hereinafter referred to as “photocuring” by irradiation with high energy rays. In addition, it is possible to provide sufficient light irradiation, particularly under the bezel, by simultaneously irradiating with high energy rays in the presence of the component (B1-1). In addition to the non-fluid reactant, the curing reaction can proceed further in the non-fluid region, and further curing reaction can proceed, and further faster curing / fast drying compared to (B1-1) alone. Can be realized. The content thereof is an amount necessary to further cure the composition to the reaction product obtained by the component (B1-1) or an amount sufficient to improve fast curability / fast dryness, preferably The amount of the metal atom in the catalyst is in the range of 1 to 50 ppm, preferably in the range of 5 to 30 ppm, with respect to the present composition.
このような、光硬化性を備えた組成設計において、成分(B1-1)と成分(B1-2)の質量比は、90/10~5/95の範囲であることが好ましく、85/15~10/90の範囲がより好ましい。質量比が前記上限以下であると、高エネルギー線照射による硬化反応の加速ができるからであり、質量比が前記下限未満であると、短時間での室温等低温での硬化反応が進行しない、すなわち、本組成物に必要な速硬化性/速乾性の硬化プロファイルが実現できなくなる場合がある。なお、高エネルギー線照射のうち、紫外線照射は、たとえば、スポットUV光源を用いて、表示装置の空隙に注入後の組成物の周囲に紫外線を照射することで行うことができる。 In such a composition design having photocurability, the mass ratio of the component (B1-1) to the component (B1-2) is preferably in the range of 90/10 to 5/95, and 85/15 A range of ˜10 / 90 is more preferred. If the mass ratio is less than or equal to the upper limit, the curing reaction can be accelerated by irradiation with high energy rays, and if the mass ratio is less than the lower limit, the curing reaction at a low temperature such as room temperature in a short time does not proceed. That is, the fast curing / fast drying curing profile required for the composition may not be realized. In addition, among high energy ray irradiation, ultraviolet irradiation can be performed by irradiating the periphery of the composition after inject | pouring into the space | gap of a display apparatus using a spot UV light source, for example.
成分(B1-2)である、高エネルギー線活性化触媒または光活性化触媒であるヒドロシリル化触媒を含む場合、本発明にかかる組成物は、組成物を調製した直後に高エネルギー線を照射した場合、25℃で少なくとも20分以内に非流動性の反応物を形成する特徴をさらに有するように設計することができる。このような組成物は、高エネルギー線を効率よく照射することが困難なベゼル下等に注入した場合であっても、スポットUV光源等を用いて補助的に光照射を行うことで、さらに迅速な硬化性および速乾性を実現できる点で、本発明にかかる表示装置用ギャップシール剤組成物の使用時に、極めて有用である。なお、本発明組成物において高エネルギー線を照射するタイミングおよび照射量は任意であり、実際の組成物の使用時に、調製した直後に高エネルギー線を照射してもよく、一定時間後に補助的に高エネルギー線を照射しても良いことはいうまでもない。また、実用的な照射量および上記の特性を規定するための照射量は前記したとおりであるが、実際の使用において、これに限定されるものではない。 When the component (B1-2), the hydrosilylation catalyst that is a high energy ray activation catalyst or a photoactivation catalyst, is included, the composition according to the present invention was irradiated with a high energy ray immediately after the composition was prepared. In some cases, it can be designed to further have the characteristic of forming a non-flowable reactant within at least 20 minutes at 25 ° C. Even when such a composition is injected under a bezel or the like where it is difficult to efficiently irradiate high energy rays, the composition can be further rapidly irradiated with light using a spot UV light source or the like. It is extremely useful when using the gap sealant composition for a display device according to the present invention in that it can realize excellent curability and quick drying. In the composition of the present invention, the irradiation timing and irradiation amount of the high energy beam are arbitrary, and when using the actual composition, the high energy beam may be irradiated immediately after the preparation, or after a certain time, Needless to say, high energy rays may be irradiated. Further, the practical irradiation amount and the irradiation amount for defining the above-mentioned characteristics are as described above, but the actual use is not limited to this.
本発明にかかる組成物は、ヒドロシリル化反応抑制剤を含まないことが好ましい。通常、組成物のポットライフを向上し安定した組成物を得るために、ヒドロシリル化反応抑制剤が組成物中に添加されるが、本発明においては、ヒドロシリル化反応抑制剤の添加によって、当該組成物の硬化反応が遅くならないことが好ましいからである。ただし、前記の注入工程における可使時間の確保の都合上、必要最小量のヒドロシリル化反応抑制剤の添加を行ってもよい。 The composition according to the present invention preferably does not contain a hydrosilylation reaction inhibitor. Usually, in order to improve the pot life of the composition and obtain a stable composition, a hydrosilylation reaction inhibitor is added to the composition. However, in the present invention, the composition can be obtained by adding a hydrosilylation reaction inhibitor. This is because it is preferable that the curing reaction of the product is not delayed. However, for the purpose of securing the pot life in the injection step, a necessary minimum amount of hydrosilylation reaction inhibitor may be added.
本発明にかかる組成物において、成分(A)が縮合反応性基を有する場合、成分(B)は(B2)縮合反応触媒を含有するものであってよい。このような縮合反応用触媒は限定されず、例えば、ジブチル錫ジラウレート、ジブチル錫ジアセテート、オクテン酸錫、ジブチル錫ジオクテート、ラウリン酸錫等の有機錫化合物;テトラブチルチタネート、テトラプロピルチタネート、ジブトキシビス(エチルアセトアセテート)等の有機チタン化合物;その他、塩酸、硫酸、ドデシルベンゼンスルホン酸等の酸性化合物;アンモニア、水酸化ナトリウム等のアルカリ性化合物;1,8-ジアザビシクロ[5.4.0]ウンデセン(DBU)、1,4-ジアザビシクロ[2.2.2]オクタン(DABCO)等のアミン系化合物が例示され、好ましくは、有機錫化合物、有機チタン化合物である。 In the composition according to the present invention, when the component (A) has a condensation reactive group, the component (B) may contain (B2) a condensation reaction catalyst. Such a catalyst for the condensation reaction is not limited, and examples thereof include organic tin compounds such as dibutyltin dilaurate, dibutyltin diacetate, tin octenoate, dibutyltin dioctate, tin laurate; tetrabutyl titanate, tetrapropyl titanate, dibutoxybis ( Organic titanium compounds such as ethyl acetoacetate; other acidic compounds such as hydrochloric acid, sulfuric acid and dodecylbenzenesulfonic acid; alkaline compounds such as ammonia and sodium hydroxide; 1,8-diazabicyclo [5.4.0] undecene (DBU) ) An amine compound such as 1,4-diazabicyclo [2.2.2] octane (DABCO) is exemplified, and an organic tin compound and an organic titanium compound are preferable.
成分(B2)の使用量は、本組成物に必要な速硬化性/速乾性の硬化プロファイルを与えるために必要な量である。なお、成分(B1)により、必要な速硬化性/速乾性の硬化プロファイルが実現可能であれば、成分(B2)の使用は任意であるが、成分(B2)を併用することにより、特に反応物の深部における硬化が経時的に進行し、表示装置のギャップフィラー組成物としてより目張り効果が改善される場合がある。 The amount of component (B2) used is that required to give the composition a fast cure / fast dry cure profile required. The component (B2) can be used arbitrarily as long as the component (B1) can achieve the required fast curing / drying curing profile. However, when the component (B2) is used in combination, the reaction is particularly effective. Curing in the deep part of the object may progress with time, and the eye-tightening effect may be further improved as a gap filler composition of a display device.
本発明にかかる組成物には、その必要に応じて、他のオルガノポリシロキサン、接着性付与剤、シリカ、ガラス、アルミナ、酸化亜鉛等の無機質充填剤;ポリメタクリレート樹脂等の有機樹脂微粉末;蛍光体、耐熱剤、染料、顔料、難燃性付与剤、溶剤等が本発明で用いるオルガノポリシロキサン組成物に添加される。添加量及びその方法は、当業者に公知である。 In the composition according to the present invention, if necessary, other organopolysiloxanes, adhesion-imparting agents, inorganic fillers such as silica, glass, alumina, and zinc oxide; fine organic resin powders such as polymethacrylate resins; A phosphor, a heat-resistant agent, a dye, a pigment, a flame retardant, a solvent and the like are added to the organopolysiloxane composition used in the present invention. The amount of addition and its method are known to those skilled in the art.
本発明にかかる組成物は、速硬化性/速乾性の硬化プロファイルを有するものであるため、二成分以上の多成分型の組成物であることが好ましい。特に、成分(A)がヒドロシリル化反応硬化性のオルガノポリシロキサンであり、成分(A1)および成分(A3)を含む場合には、これらの成分を異なるパッケージとした二成分以上の多成分型の組成物として取扱い、使用直前に混合するか、前記のような吐出時の混合機構を備えたディスペンサーを用いて目的とする表示装置の空隙に注入することが好ましい。 Since the composition according to the present invention has a fast-curing / fast-drying curing profile, it is preferably a multi-component composition of two or more components. In particular, when the component (A) is a hydrosilylation reaction-curable organopolysiloxane and includes the component (A1) and the component (A3), a multicomponent type of two or more components in which these components are different packages is used. It is preferable to handle it as a composition and mix it immediately before use, or inject it into the gap of the target display device using a dispenser equipped with a mixing mechanism as described above.
より具体的には、本組成物は、上記成分(A)、成分(B)、および必要に応じて、その他任意の成分を室温下で均一に混合することにより製造することができる。 More specifically, the present composition can be produced by uniformly mixing the above component (A), component (B), and other optional components as necessary at room temperature.
特に好適には、本組成物は、少なくともヒドロシリル化反応硬化性を有する、2成分型(=2液型)の組成物であることが好ましく、
I液成分が、前記の前記の成分(A1)および成分(B)を少なくとも含有し、任意でその他の成分を含み、
II液成分が、前記の成分(A2)成分を少なくとも含有するものであり、
それぞれ、室温下、密閉容器中に封入することにより長期間貯蔵することが可能である。これらを混合した直後において液状かつ一定の初期粘度を有すること、および、速硬化性/速乾性の硬化プロファイルを有する旨は前記のとおりである。
Particularly preferably, the composition is preferably a two-component (= 2 liquid) composition having at least hydrosilylation reaction curability,
The component I component contains at least the aforementioned component (A1) and component (B), and optionally includes other components,
The II liquid component contains at least the component (A2),
Each can be stored for a long period of time by being sealed in a sealed container at room temperature. As described above, immediately after mixing them, it has a liquid and constant initial viscosity and has a fast curing / fast drying curing profile.
本発明は、前記組成物を表示装置用のギャップシール剤組成物として使用することを特徴の一つとし、特に、表示装置が、ベゼルと表示パネルを備えた画像表示装置であり、当該ベゼルと当該表示パネルとの間隙を充填する目的で組成物を使用することが好ましい。なお、上記目的における使用は、前記ベゼルと表示パネルの間の空隙間に、表示パネルに対して垂直方向に当該空隙を隙間なく充填する機能を有する部材として、本組成物を硬化させてなるシリコーン樹脂部材を利用することを含む。 One feature of the present invention is that the composition is used as a gap sealant composition for a display device. In particular, the display device is an image display device including a bezel and a display panel. It is preferable to use the composition for the purpose of filling the gap with the display panel. In addition, the use for the said objective is the silicone which hardens this composition as a member which has a function which fills the said space | gap with the space | interval between the said bezel and a display panel perpendicularly | vertically with respect to a display panel. This includes using a resin member.
本発明にかかる組成物は、硬化してエラストマー(弾性体)樹脂部材またはゲル状樹脂部材を形成することが好ましく、硬化後のシリコーン樹脂部材にあっては、25℃において、そのJIS K2220で規定される針入度(以下、単に「針入度」という)が、5~70の範囲にあることが好ましく、針入度が10~60の範囲、20~50の範囲にあることがより好ましい。このようなシリコーン樹脂部材は、適度な柔軟性と耐久性を有し、部材間の接着/密着保持性と追従性に優れるため、表示装置用のギャップシール剤組成物として使用することで、確実な目張り効果を実現することができる。 The composition according to the present invention is preferably cured to form an elastomer (elastic body) resin member or a gel-like resin member. The cured silicone resin member is defined by JIS K2220 at 25 ° C. The penetration (hereinafter simply referred to as “penetration”) is preferably in the range of 5 to 70, more preferably in the range of 10 to 60 and in the range of 20 to 50. . Such a silicone resin member has moderate flexibility and durability, and is excellent in adhesion / adhesion retention and followability between the members. Therefore, it can be reliably used as a gap sealant composition for a display device. It is possible to realize a glazing effect.
本発明にかかる組成物は、ベゼルと表示面との重なり部位に生じた間隙を充填する目的で利用されるので、硬化して接着性を有し、かつ、最大接着強度における試料の変形が十分に大きい樹脂部材を形成することが好ましい。具体的には、硬化後のシリコーン樹脂部材にあっては、25℃において、そのJIS K6850に準拠して測定される引張剪断接着強度(以下、単に「剪断接着強度」という)が0.05 MPa以上であることが好ましく、0.05~10MPaの範囲であることがより好ましく、実用上、0.1~5MPaの範囲の範囲であってもよい。また、同樹脂部材について、引張剪断接着強度のピーク値(=最大接着強度)における試料厚みに対する引張り剪断変位量を測定した場合、変位の割合が1000%以上であることが好ましく、実用上、同割合が1000~6000%の範囲であることが好ましい。このような接着性および最大接着強度における試料の変形が十分に大きい樹脂部材を用いることで、部材間が強固に接着され、かつ多少の変形においても部材からのダム材の剥離や空隙を生じないため、本発明にかかる表示装置用のギャップシール剤組成物として使用することで、確実な目張り効果を実現することができる。 Since the composition according to the present invention is used for the purpose of filling the gap formed at the overlapping portion of the bezel and the display surface, it is cured and has adhesiveness, and the sample is sufficiently deformed at the maximum adhesive strength. It is preferable to form a large resin member. Specifically, in the cured silicone resin member, the tensile shear adhesive strength (hereinafter simply referred to as “shear adhesive strength”) measured at 25 ° C. according to JIS K6850 is 0.05 μMPa. The above is preferable, more preferably in the range of 0.05 to 10 MPa, and practically in the range of 0.1 to 5 MPa. Further, when the tensile shear displacement amount with respect to the sample thickness at the peak value of tensile shear adhesive strength (= maximum adhesive strength) is measured for the same resin member, the displacement ratio is preferably 1000% or more. The proportion is preferably in the range of 1000 to 6000%. By using a resin member that has a sufficiently large deformation of the sample in such adhesiveness and maximum adhesive strength, the members are firmly bonded to each other, and the dam material does not peel from the member or cause a gap even with some deformation. Therefore, by using as a gap sealant composition for a display device according to the present invention, it is possible to achieve a reliable cover effect.
[表示装置の製造方法および表示装置]
本発明は、上記の表示装置用のギャップシール剤組成物の使用を特徴の一つとする表示装置の製造方法および表示装置に関する。
[Display device manufacturing method and display device]
The present invention relates to a display device manufacturing method and a display device characterized by the use of the gap sealant composition for a display device described above.
以下、添付図面を参照しながら、本発明を実施するための形態(以下「実施形態」という。)について説明する。なお、本明細書及び図面において、多少異なっていても実質的に同一の構成要素については同一の符号を用いる。図面に描かれた形状は、当業者が理解しやすいように描かれているため、実際の寸法及び比率とは必ずしも一致していない。断面図は切断面のみを示し奥行きの構造は省略する。本明細書及び特許請求の範囲における「備える」とは、明示した要素以外の要素を備える場合も含まれる。「有する」や「含む」なども同様である。また、「樹脂部材」とは、上記のギャップシール剤組成物が硬化してなるシリコーン樹脂部材を意味するものである。 Hereinafter, embodiments for carrying out the present invention (hereinafter referred to as “embodiments”) will be described with reference to the accompanying drawings. In the present specification and drawings, the same reference numerals are used for substantially the same components even if they are slightly different. The shapes depicted in the drawings are drawn so as to be easily understood by those skilled in the art, and thus do not necessarily match the actual dimensions and ratios. The sectional view shows only the cut surface, and the depth structure is omitted. The term “comprising” in the present specification and claims includes a case of including elements other than the specified elements. The same applies to “having” and “including”. The “resin member” means a silicone resin member obtained by curing the gap sealant composition.
まず、本発明の製造方法を用いて得られる表示装置について、図1および図2に記載の本発明の実施形態1に基づき説明する。 First, a display device obtained by using the manufacturing method of the present invention will be described based on Embodiment 1 of the present invention shown in FIG. 1 and FIG.
図1に示すように、本発明にかかる表示装置203は、表示面11を有する表示パネル10と、枠部21と枠部21の内側の開口端22とを有し、表示パネル10の表示面11側の周縁を枠部21で覆うベゼル20と、表示パネル10の表示面11側にベゼル20を挟んだ状態で設けられた前面パネル30と、ベゼル20の開口端22の直下であって、ベゼル20と表示面11との重なり部位に生じた間隙72を表示面11に対して垂直方向に空隙を有さずに充填する樹脂部材40と、表示面11と前面パネル30との間に充填されたOCR50と、を備えている。ここで、表示面11とは、偏光板12の前面パネル30側の面全域を指す(以下同じ)。
As shown in FIG. 1, a display device 203 according to the present invention includes a
CF基板13とTFT基板14とが液晶(図示せず)を介して対向して設けられ、CF基板13の外側及びTFT基板14の外側にそれぞれ偏光板12,15が設けられることにより、表示パネル10が構成されている。バックライトユニット71上に表示パネル10が搭載され、ベゼル20とバックライトユニット71とが嵌合構造(図示せず)により固定されることにより、表示モジュール70が構成されている。表示モジュール70とタッチパネル等の前面パネル30とは、OCR50を介して全面が貼り合されている。ここで、樹脂部材40は、ベゼル20と表示面11との重なり部位に生じた間隙72を表示面11に対して垂直方向に空隙を有さないように設けられる。当該構造では、樹脂部材40はベゼル20と表示面11との重なり部位のみに設けられているため、表示領域18には実質的な影響を与えず、ベゼル20が仮に幅の狭い構造であるとしても、完成した表示装置において表示ムラの原因となることはなく、その表示品質、特にベゼル端部に近い部位における表示品質および操作性を改善する。さらに、樹脂部材40は、ベゼル20と表示面11とを垂直方向に空隙なく充填するため、OCR50の溢れ出しを効果的に抑制して、いわゆる「目張り」の目的を確実に達成し、表示装置の耐久性を向上させ、生産時における不良品の発生率を低下させ、歩留まりおよび表示品質をさらに改善可能である。
A CF substrate 13 and a
なお、上記のとおり、樹脂部材40は、ベゼル20と表示面11とを垂直方向に空隙なく充填する構造であって、表示領域18やベゼル20上に跨がる構造を有しないため、本構造においては表示領域18を最大化することができる一方、ベゼル20上に樹脂部材40に由来する突起や凹凸構造を何ら生じないため、特許文献2等で提案されている樹脂部材をベゼル20上に跨らせて空隙72を塞ぐ構造に比べて、ベゼル上の凹凸や寸法(高さ)のばらつきが生じにくく、図2におけるベゼル20の表面23と前面パネル30との距離を一定に保持できるため、ベゼル20の外周上に配した接着部材60により前面パネル30が高い平坦性をもって配置され、外観不良及び接着不良となることを防止できる。なお、ベゼル20下の間隙72内を充填する樹脂部材40が確実な目張り効果を有するため、OCR50が表示パネル10下やバックライトユニット71に溢れ出すことはない。
Note that, as described above, the
このような実施形態1の表示装置は、図3Aおよび図3Bに示すように、間隙72に対して注入角が、水平~75度の範囲となる角度で本発明の表示装置用のギャップシール剤組成物を注入して充填する工程を備えた表示装置の製造方法により得ることができる。特許文献2等で提案されているように、間隙72に対する注入角が垂直方向であると、図5のようにベゼル20と表示面11との重なり部位に生じた間隙72をその外側から塞ぐ構造となり、目張りが不十分となって、OCR50が表示パネル10下やバックライトユニット71に溢れ出す結果となる。これは、後述する実施例に対する参考例において検証されている。
As shown in FIGS. 3A and 3B, the display device according to the first embodiment has a gap sealant for a display device according to the present invention at an angle with respect to the
ここで、表示装置用のギャップシール剤組成物を間隙72に対して注入角が水平~75度となる角度で注入する手段として、L字型、略L字型または可とう性の吐出口から選ばれる少なくとも1種類の吐出口を備えた注入装置が好適に用いられる。より具体的には、L字型ノズル、略L字型ノズルまたは可とう性ノズルを備えたシリンジまたはディスペンサーを用いて当該間隙72に対して注入角が水平(=0度)~75度となる角度、より好適には、注入角が水平(=0度)~45度、特に好適には注入角が水平(=0度)~30度となる角度、最も好適には、当該間隙72に対して実質的に水平(=0度)となる注入角をもって表示装置用のギャップシール剤組成物を注入する工程を備えることが、本発明の表示装置の製造方法において、好ましい。このようなL字型ノズル等を備えた注入装置は、例えば、L字ニードル(武蔵エンジニアリング株式会社製 武蔵カーブニードル CPN-18G-A90)を備えたシリンジやディスペンサーが市販されている。
Here, as a means for injecting the gap sealant composition for the display device at an angle with which the injection angle is horizontal to 75 degrees with respect to the
なお、水平注入において真っ直ぐなニードルを採用することは、図2に明示するように枠上のベゼル20を配置した状態では短距離四方に障害物となる構造体が配置されているため、実質的に不可能であり、L字ノズル/ニードル、略L字ノズル/ニードルまたはゴム製のノズル/ニードルのように折れ曲げることができる可とう性ノズルを備えた注入装置の使用が必要になる。
Note that the use of a straight needle in horizontal injection is substantially because a structure that serves as an obstacle is disposed in a short-distance direction in a state where the
より具体的には、本製造方法において、まずベゼル20の開口端22に沿って表示パネル10の表示面11に、L字ノズルを備えたディスペンサ装置によって、吐出口が間隙72に対して実質的に水平方向となるように、表示装置用のギャップシール剤組成物を定速かつ定量で注入(図3A)しながら、当該ダム材の注入の軌跡を追いかけるようにスポット用UV光源でUV光を照射して、ベゼル20と表示面11との重なり部位に生じた間隙72の内側に樹脂部材40を形成した(図3B)。なお、本発明にかかる表示装置用のギャップシール剤組成物は速硬化性/速乾性の硬化プロファイルを有するので、UV光を照射する前に非流動性の反応物を形成しており、当該反応物がUV光の照射により、さらに硬化するものであってもよく、UV光の照射を省略してもよい。なお、ダム材となる硬化性樹脂組成物を注入する際には、L字ノズルの先端が間隙72の内側に挿入された状態で定速かつ定量で注入を行うことが特に好ましい。
More specifically, in this manufacturing method, first, the discharge port is substantially formed with respect to the
本発明にかかる製造方法および表示装置において、ベゼルと表示面との重なり部位に生じた間隙を充填する目的で利用可能な表示装置用のギャップシール剤組成物およびその硬化手段は、上記のとおりであり、短時間での硬化が可能であり、表示装置の各部材に悪影響を及ぼさない見地から、室温におけるヒドロシリル化反応、UV光の照射による光硬化(光反応性ヒドロシリル化触媒の使用を含む)を主たる硬化手段とする硬化システムを選択することが好ましい。 In the manufacturing method and the display device according to the present invention, the gap sealant composition for a display device that can be used for the purpose of filling a gap formed at the overlapping portion of the bezel and the display surface and the curing means thereof are as described above. Yes, it can be cured in a short time and does not adversely affect each component of the display device. From the standpoint of not adversely affecting each member of the display device, photo-curing by UV light irradiation (including the use of photoreactive hydrosilylation catalyst) It is preferable to select a curing system in which is the main curing means.
なお、実施形態1の表示装置においてその寸法は特に限定されるものではなくベゼルの開口端から表示領域までの設計寸法は0.1~10mm、好適には、0.2~5mmの範囲で設計するのが一般的である。たとえば、表示モジュール70は、ベゼル20の開口端22から表示領域18までの設計寸法が1.5mmであるのに対し、表示パネル10とベゼル20との間隙72は0.2mm、ベゼル20の厚さは0.3mmの範囲で設計してよい。しかしながら、各種のばらつきによって、間隙72の実際の寸法、すなわち、表示パネル10の表示面11からベゼル20の表面23までの距離は、そのままベゼル20を表示パネル上に配置すると大きなばらつきを生じ、これが、表示装置用のギャップシール剤組成物を定速かつ定量で注入した場合に、間隙72に対する充填不良の原因となる場合がある。このような充填不良があると同間隙72を十分に塞ぐことができずに隙間が生じるため、OCR注入後、同隙間からOCRが表示モジュールの内部にしみ込んで漏洩する原因となり、表示品質の低下や表示装置の耐久性の低下を引き起こす場合がある。
The dimensions of the display device of Embodiment 1 are not particularly limited, and the design dimension from the open end of the bezel to the display area is 0.1 to 10 mm, preferably 0.2 to 5 mm. It is common to do. For example, the
本発明においては、吐出口が間隙72に対して実質的に水平方向となるように、表示装置用のギャップシール剤組成物を注入するため、垂直方向から間隙72を塞ぐアプローチ(図5、特許文献1または特許文献2等)に比べて、このような充填不良は発生しにくいが、より確実にベゼルと表示パネルとの間隙を目張りし、確実な充填を行うため、以下の表示装置の製造方法が好適に採用できる。
In the present invention, in order to inject the gap sealant composition for the display device so that the discharge port is substantially horizontal with respect to the
すなわち、ベゼルと表示パネルとの間隙のばらつきはベゼルのうねりに由来するため、両者をそのまま配置するのではなく、予め、前記ベゼルと表示パネルの間の空隙間に、表示パネルに対して垂直方向に当該空隙を隙間なく充填する機能を有する部材を配置した後に、前記のギャップシール剤組成物を注入して充填することでベゼルと表示パネルとの間隙の高さのばらつきを解消ないし低減することができる。 That is, since the variation in the gap between the bezel and the display panel is derived from the swell of the bezel, the two are not arranged as they are, but in advance between the bezel and the display panel in the direction perpendicular to the display panel. After disposing a member having a function of filling the gap without gaps, the gap sealant composition is injected and filled to eliminate or reduce the variation in the gap height between the bezel and the display panel. Can do.
このような部材は、部材間の高さを一定に保持する機能に加えて、注入された前記のギャップシール剤組成物に対して物理的または化学的に親和性を有するので、垂直方向への漏洩を防止し、充填時の起点ないし終点として用いることで、より効果的な目張りを実現することができる。 Such a member has a physical or chemical affinity to the injected gap sealant composition in addition to the function of keeping the height between the members constant. Leakage can be prevented and more effective weathering can be realized by using as a starting point or an ending point at the time of filling.
このような部材は、ベゼルと表示パネルとの間隙に充填する樹脂部材と同一または異なる硬化性樹脂組成物を硬化させてなる樹脂部材であってよいが、ともに、本発明にかかる表示装置用のギャップシール剤組成物を硬化させてなるシリコーン樹脂部材であることが好ましい。これらの樹脂部材は表示パネル上にうねりを有するベゼルを配置する際に、両部材間で仮の支えとなって、その間隙の高さを調整する機能を有するため、一点よりも二点以上が好ましく、三点以上がより好ましく、四点以上が特に好ましい。最も好適には、当該樹脂部材が、四隅または少なくとも四点が略対角線上に配置されていることである。特に、これらの樹脂部材が、これらの樹脂部材がベゼルと表示パネルとの間隙を充填する目的で注入される硬化性樹脂組成物を硬化させてなる樹脂部材と同一である場合、注入時の起点や終点(中間点を含む)に配置された樹脂部材に、吐出口から注入された未硬化の硬化性樹脂組成物が接触すると、両者間の界面が界面張力的に良好な親和性を有するために、当該硬化性樹脂組成物が注入された間隙の全領域で均一に広がって偏りを生じにくくなり、いわゆる「引け」に伴う充填不良が効果的に抑制される。すなわち、保持材としての樹脂部材と、上記のベゼルと表示パネルとの間隙を充填する目的で使用される樹脂部材として同一の硬化性樹脂組成物を硬化させてなる樹脂部材を選択することにより、充填時に樹脂部材が一部に偏って充填不良が起こることを抑制し、間隙全領域をより確実に目張りすることができる利点がある。 Such a member may be a resin member obtained by curing the same or different curable resin composition as the resin member filled in the gap between the bezel and the display panel, and both are for the display device according to the present invention. A silicone resin member obtained by curing the gap sealant composition is preferred. Since these resin members have a function of adjusting the height of the gap between the two members when the bezel having waviness is arranged on the display panel, the resin member has a function of adjusting the height of the gap. Preferably, three or more points are more preferable, and four or more points are particularly preferable. Most preferably, the resin member has four corners or at least four points arranged on substantially diagonal lines. In particular, when these resin members are the same as resin members obtained by curing a curable resin composition injected for the purpose of filling the gap between the bezel and the display panel, the starting point at the time of injection When the uncured curable resin composition injected from the discharge port comes into contact with the resin member placed at the end point (including the intermediate point), the interface between the two has good affinity for interfacial tension In addition, it spreads uniformly in the entire region of the gap into which the curable resin composition has been injected and is less likely to be biased, so that filling defects associated with so-called “shrinkage” are effectively suppressed. That is, by selecting a resin member obtained by curing the same curable resin composition as a resin member used as a holding member and a resin member used for filling the gap between the bezel and the display panel. There is an advantage that it is possible to prevent the resin member from being partially biased during filling and to prevent poor filling, and it is possible to more reliably cover the entire gap region.
換言すれば、本発明の好適な表示装置の製造方法は、前記ベゼルの前記開口部の全周の少なくとも一点において、予め前記ベゼルと表示パネルの間の空隙に、表示パネルに対して垂直方向に当該空隙を隙間なく充填する機能を有する部材を配置した後、前記ベゼルの前記開口部の全周において、前記ベゼルと表示パネルの間の空隙を、当該空隙に対する注入角が、水平~75度の範囲となる角度で本発明の表示装置用ギャップシール剤組成物を注入して充填する工程
を含むことを特徴とする。このような部材間の空隙を表示パネルに対して垂直方向に隙間なく充填する目的で設けられる目的で設けられる樹脂部材は、表示パネル上の表示面であり、ベゼルを配置した場合に、前記開口部の全周において、その四隅または縦方向および横方向の軸上に各一点ずつ、計四点以上となるように設けられていることが好ましい。これらの樹脂部材からなる保持材を表示面に設けた後に、うねりを有するベゼルを配置することで、表示パネルの表示面からベゼルの表面までの距離、すなわち間隙の高さを効果的に調整し、そのばらつきを抑制ないし最小化し、さらに、本発明にかかるギャップシール剤組成物への親和性を改善することで、垂直方向への漏洩を効果的に抑制し、その注入時の起点乃至終点として機能するので、注入されるギャップシール剤組成物が流動して充填不良が発生することを抑制することができる。これにより、本発明のギャップシール剤組成物を当該間隙に水平方向~75度の注入角で定速かつ定量で注入した場合に、間隙に対する充填不良がさらに抑制され、確実な充填が達成される。
In other words, in a preferable method for manufacturing a display device of the present invention, at least at one point of the entire circumference of the opening of the bezel, a gap between the bezel and the display panel is previously provided in a direction perpendicular to the display panel. After disposing a member having a function of filling the gap without any gaps, the gap between the bezel and the display panel is set to a horizontal to 75 degree injection angle with respect to the gap on the entire periphery of the opening of the bezel. It includes the step of injecting and filling the gap sealant composition for a display device of the present invention at an angle within a range. The resin member provided for the purpose of filling the gap between the members in the vertical direction with respect to the display panel without any gap is a display surface on the display panel, and when the bezel is disposed, In the entire circumference of the part, it is preferable to provide four points or more on each of the four corners or the longitudinal and lateral axes. After the holding material made of these resin members is provided on the display surface, the bezel having the waviness is arranged to effectively adjust the distance from the display surface of the display panel to the surface of the bezel, that is, the height of the gap. In addition, by suppressing or minimizing the variation, and further improving the affinity to the gap sealant composition according to the present invention, the leakage in the vertical direction is effectively suppressed, and the starting point or the ending point at the time of injection Since it functions, it can suppress that the gap sealing agent composition inject | poured flows and a poor filling generate | occur | produces. As a result, when the gap sealant composition of the present invention is injected into the gap at a constant speed and in a constant amount at an injection angle of ˜75 degrees in the horizontal direction, filling defects in the gap are further suppressed, and reliable filling is achieved. .
より具体的には、図4に示すとおり、本発明の実施形態1における表示パネル10の表示面11の端部であって、ベゼル20を配置した場合にその開口端22の内側となる部位に樹脂部材(本発明の表示装置用のギャップシール剤組成物)からなる保持材である樹脂部材41を事前に配置し(図4A)、同保持材によって高さを保持した状態でベゼル20が配置される(図4B)。これにより、表示パネルの表示面からベゼルの表面までの距離、すなわち間隙72の高さが効果的に調整され、かつ、その後に全周に注入されるギャップシール剤組成物の充填不良が抑制されるものである。図示しないが、ベゼル20は四角形状であるので、その四隅または各辺上の1点以上、計四点以上において同様な間隙72の高さの事前調整を行うことで、本発明のギャップシール剤組成物を当該間隙に水平方向~75度の注入角で定速かつ定量で注入した場合に、間隙に対する充填不良がさらに抑制され、確実な充填が達成される。
More specifically, as shown in FIG. 4, in the end portion of the
なお、本発明にかかる製造方法および表示装置において、間隙の保持材である樹脂部材の形成に用いる硬化性樹脂組成物は特に制限されるものではなく、前記のダム材である硬化性樹脂組成物として例示したものと同一であっても異なってもよい。作業工程の簡便性の見地から、前記のギャップシール剤組成物として好適に例示したものと同種の硬化性のシリコーン樹脂組成物を使用してよく、かつ好ましい。 In the production method and display device according to the present invention, the curable resin composition used for forming the resin member that is the gap holding material is not particularly limited, and the curable resin composition that is the dam material. May be the same as or different from those exemplified. From the viewpoint of simplicity of the working process, a curable silicone resin composition of the same kind as that preferably exemplified as the gap sealant composition may be used and is preferable.
上記の間隙の高さを効果的に調整する見地から、保持材である樹脂部材の高さは各点において概ね同一であることが好ましい。ただし、上記の硬化性樹脂組成物を硬化してなる樹脂部材は接着性かつ弾性体またはゲル状硬化物を選択可能であり、このような弾性体またはゲル状硬化物を用いることで、樹脂部材の高さが多少不揃いであったとしても、ベゼル同樹脂部材上に配置した際に樹脂部材が変形し、全体の間隙の高さが概ね同一となるように調整される利点がある。 From the viewpoint of effectively adjusting the height of the gap, it is preferable that the height of the resin member as the holding material is substantially the same at each point. However, the resin member obtained by curing the curable resin composition can be selected from an adhesive and an elastic body or a gel-like cured product. By using such an elastic body or a gel-like cured product, the resin member Even if the heights are somewhat uneven, there is an advantage that the resin member is deformed when arranged on the resin member of the bezel, and the overall gap height is adjusted to be substantially the same.
本発明にかかる製造方法および表示装置は、さらに、OCRである硬化性樹脂組成物を用いて、表示パネルと前面パネル間を貼り合せた構造およびそれにかかる工程を有する。 The manufacturing method and display device according to the present invention further have a structure in which a display panel and a front panel are bonded together using a curable resin composition that is OCR, and a process related thereto.
すなわち、本発明にかかる製造方法は、前記のベゼルと表示パネルの間の間隙に硬化性樹脂組成物を注入して充填する工程の後、
さらに、
前記表示パネルの前記表示面側に、前記と同一又は異なる硬化性樹脂組成物を塗布する工程、および、
当該硬化性樹脂組成物を塗布した表示面側に、前記ベゼルを挟んだ状態で前面パネルを貼り付ける工程
を含む。本発明においては、前記の表示装置用のギャップシール剤組成物が硬化してなるシリコーン樹脂部材が、OCRである硬化性樹脂組成物に対する目張りを確実に達成し、OCRの塗布時または注入時において同間隙の隙間からOCRが漏洩して表示モジュール内部にしみ込むことが防止されるので、得られる表示装置において高い表示品質および耐久性を実現し、製造時の不良の発生を抑制して、歩留まりを改善することができる。
That is, in the manufacturing method according to the present invention, after the step of injecting and filling the curable resin composition into the gap between the bezel and the display panel,
further,
Applying the same or different curable resin composition to the display surface side of the display panel; and
A step of attaching a front panel to the display surface side to which the curable resin composition is applied with the bezel sandwiched therebetween. In the present invention, the silicone resin member formed by curing the gap sealant composition for a display device reliably achieves the cover for the curable resin composition that is OCR, at the time of application or injection of OCR. Since OCR leaks from the gap and penetrates into the display module, it is possible to achieve high display quality and durability in the resulting display device, and to suppress the occurrence of defects during manufacturing, thereby reducing yield. Can be improved.
本発明の実施形態1においては、間隙72を樹脂部材40で充填した後、OCR50を全面塗布し、ベゼル20の外周全域に接着剤60を塗布し、前面パネル30としてのタッチパネルを減圧環境下で全面貼り合せてからUV照射で本硬化させる。このような一連の製造プロセスによって図2に示す表示装置101が完成する。当該実施形態1の表示装置101の製造プロセスは、前記のダム材である樹脂部材40による間隙72を充填する工程およびそれに先立ち、同間隙72の高さを保持材により事前調整する工程を除いては、一般的なオプティカルボンディングのプロセスに準ずるものであり、表示装置のオプティカルボンディングのプロセスとして汎用性を有するものである。
In Embodiment 1 of the present invention, after filling the
なお、本実施形態1の製造方法においては、ダム材である樹脂部材および間隙72の保持材である樹脂部材を形成する表示装置用のギャップシール剤組成物は、ともに、その塗布と同時にUV照射して仮硬化させたが、これらの表示装置用のギャップシール剤組成物の粘度が十分に高く、塗布形状を一定時間維持できる場合は、全周塗布後に一括UV照射してもよいし、場合によってはUV仮硬化自体も不要である。なお、本発明(本実施形態1)にかかる製造方法および表示装置においては、これらの樹脂部材は、ベゼル20の直下、すなわち、表示領域の外側に形成されるので、当該樹脂部材の硬化によって、オプティカルボンディングに用いるOCRとの屈折率差によって境界が視認されやすくなる等の問題は本質的に解決されている。すなわち、従来技術(特許文献1または特許文献2等)では問題となることがあった、間隙72を塞ぐ目的で配置された樹脂部材とOCRとの屈折率差に由来する表示品質・性能の劣化の問題に対し、本発明は本質的な解決策を提供するものである。
In the manufacturing method of the first embodiment, the gap sealant composition for a display device that forms the resin member that is a dam material and the resin member that is a holding material for the
なお、本実施形態1の製造方法において、前面パネルを有する表示装置を製造する上で必要となるOCR塗布工程(オプティカルボンディングの場合)、又は貼り合せ工程等については前記減圧環境下に限定されることなく、大気圧環境下における公知の貼り合せ方法を採用してもよい。例えば大気圧環境下で前面パネル側にOCRを塗布し、前面パネルを反転させて表示モジュールと貼り合せる方式(反転貼り合せ方式)や、前面パネルと表示モジュールとの間に所定のギャップ量を確保して平行配置し、そのギャップ間にOCRを充填する方法(ギャップディスペンス方式)などであってもよい。 In the manufacturing method according to the first embodiment, the OCR coating process (in the case of optical carburizing) or the bonding process required for manufacturing a display device having a front panel is limited to the above-described reduced pressure environment. Without limitation, a known bonding method under an atmospheric pressure environment may be employed. For example, OCR is applied to the front panel in an atmospheric pressure environment, and the front panel is inverted and bonded to the display module (reverse bonding method), or a predetermined gap is secured between the front panel and the display module. Alternatively, a method of arranging them in parallel and filling OCR between the gaps (gap dispensing method) may be used.
次に、本実施形態1の表示装置101の効果について説明する。 Next, effects of the display device 101 according to the first embodiment will be described.
本実施形態1によれば、開口端22と表示パネル10との間隙72が樹脂部材40によって完全に目張りされており、かつ、当該樹脂部材40がベゼル20の下に形成されているため、製造工程でダムが壊れることがなく、未硬化のOCR50が表示モジュール70の内部にしみ出すおそれがないため、表示信頼性の高い表示装置101を提供できる。さらに、当該樹脂部材40は、表示領域に掛からないため、OCRとの屈折率差に由来する端部における表示ムラ等の表示品質および表示性能の劣化の問題、およびそれに由来する操作性の低下等の問題が本質的に解決される。
According to the first embodiment, the
加えて、本実施形態1によれば、開口端22と表示パネル10との間隙72との距離を事前に保持材である樹脂部材41によって予め一定に保持し、かつ、注入される本発明の表示装置用のギャップシール剤組成物に対して親和性を向上させ、注入時の起点/終点として機能させることができるため、定量かつ定速でギャップシール剤組成物を間隙72に注入した場合でも確実な目張りが達成でき、工業的生産性に優れる。また、当該樹脂部材40は、ベゼル20の下に形成されるため、ベゼル20上に前面パネル30を配置した場合に、目張りに用いた樹脂部材40に由来する凹凸が生じることはなく、前面パネルの取り付け時の外観不良及び接着不良となることを防止できる。
In addition, according to the first embodiment, the distance between the opening
なお、本実施形態1における表示パネル10と前面パネル30とは、全面をOCRにより貼り合わせた構造となっているが、当該構造を、空気層を隔てて貼り合された構造(エアギャップボンディング)に変更してもよい。
In addition, although the
本実施形態1において、ベゼル20上に接着部材60が配置されているが、これは、表示面11上のOCR50に剥離方向の外力Fが働いた場合に、前面パネル30とOCR50との剥離に対して耐性を向上させる目的である。その結果、表示モジュール70よりも外形の大きな前面パネル30の貼り合せ時であっても、表示面11上のOCR50が剥がれてしまうようなストレスがかからないように、確実な接着補強をすることができる。なお、接着部材60の接着強度は、OCR50よりも強いことが補強目的の観点から望ましいが、OCR50と同等以上であれば一定の補強効果を得ることができる。また、OCR50が高い接着強度を有する場合、接着部材60がなくてもよい。すなわち、本実施形態1において、接着部材60は任意の構成要素である。なお、表示モジュール70と前面パネル30との間に、さらに導電層を備えたシールド基板等を挿入する場合、当該接着部材60は、導電性材料(=導電性接着剤)であることが好ましい。
In the first embodiment, the
本発明にかかる製造方法および表示装置において、当該表示装置は、前記表示面と前面パネルとの間が実質的に透明な光学弾性体樹脂部材または光学ゲル状樹脂部材により充填された構造を備えた表示装置であることが好ましい。このような光学弾性体樹脂部材または光学ゲル状樹脂部材をOCRとして、オプティカルボンディングに用いることで、当該表示装置の表示性能および耐久性を改善し、高信頼性の表示装置を提供できる。 In the manufacturing method and the display device according to the present invention, the display device has a structure in which a space between the display surface and the front panel is filled with a substantially transparent optical elastic resin member or optical gel resin member. A display device is preferred. By using such an optical elastic resin member or optical gel resin member as OCR for optical carving, the display performance and durability of the display device can be improved, and a highly reliable display device can be provided.
このようなOCRは硬化性樹脂組成物を硬化させてなることが好ましく、前記の針入度、せん断接着強度、および最大接着強度で試料厚みに対する変位の割合にかかる物理的性質を有し、UV光の照射を含む光硬化により形成された、シリコーン樹脂硬化物(部材)が例示される。 Such an OCR is preferably formed by curing a curable resin composition, and has physical properties relating to a ratio of displacement with respect to a sample thickness at the above-described penetration, shear adhesive strength, and maximum adhesive strength, and UV. The silicone resin hardened material (member) formed by photocuring including light irradiation is illustrated.
このようなOCRは特に限定されるものではないが、東レ・ダウコーニング/DowCorning製 EG-1200、EG-4131、VE-6001 UVなど;ワッカー社製 SilGel 612 PT、 LUMISIL 100、LUMISIL 102の市販品を利用可能である。なお、本発明のギャップシール剤組成物は、OCRとして用いてもよく、両者の屈折率および硬さ等物理的性質の差を最小化したり、付着性・封止性等をさらに改善できる場合がある。 Such OCR is not particularly limited, but is commercially available from Toray Dow Corning / Dow Corning, EG-1200, EG-4131, VE-6001600UV, etc .; manufactured by Wacker, SilGel 612 PT, LUMISIL 100, LUMISIL 102 Is available. The gap sealant composition of the present invention may be used as an OCR, and may minimize differences in physical properties such as refractive index and hardness of the two, or may further improve adhesion and sealing properties. is there.
本発明にかかる製造方法および表示装置において、当該表示装置は、さらに、
前記前面パネルの前記表示面に対向する面に設けられ、透明導電膜が形成された面を有するシールド基板を更に備え、
前記透明導電膜と前記ベゼルとが導電性材料を介して電気的に接続された構造を備えた表示装置であってよい。
In the manufacturing method and the display device according to the present invention, the display device further includes:
A shield substrate provided on a surface of the front panel facing the display surface and having a surface on which a transparent conductive film is formed;
The display device may include a structure in which the transparent conductive film and the bezel are electrically connected via a conductive material.
たとえば、上記の実施形態1における表示装置101(図1)において、表示モジュール70と前面パネル30との間に、さらに、片面に導電層を備えたEMI(Electro-Magnetic Interference)基板等のシールド基板を挿入することができる。このようなシールド基板は電磁波遮蔽機能を有するので、表示モジュール70から放射される電磁波によって前面パネル30が誤動作することを防ぐ。また、当該シールド基板の片面には、ITO(Indium Tin Oxide)等の透明導電膜からなる導電層が一様に又はメッシュ状に形成されている。そして、当該導電層の電位を表示モジュール70のGNDに設定するため、ベゼル20の外周に配置する接着部材60等を、例えばAgペースト等の導電性接着部材で形成することもできる。なお、表示モジュール70のベゼル20は、金属製であり、表示モジュール70内でGND接続されている。ここで、接着部材60を導電性材料とすることで、金属製のベゼル20と前記のシールド基板の導電層とを確実にGND接続できるため、電磁波耐性の強い表示装置を提供することができる。
For example, in the display device 101 (FIG. 1) according to the first embodiment, a shield substrate such as an EMI (Electro-Magnetic Interference) substrate provided with a conductive layer on one side between the
以上、上記実施形態を参照して本発明を説明したが、本発明は上記各実施形態に限定されるものではない。本発明の構成や詳細については、当業者が理解し得るさまざまな変更を加えることができる。また、本発明には、上記各実施形態の構成の一部又は全部を相互に適宜組み合わせたものも含まれる。 Although the present invention has been described with reference to the above embodiment, the present invention is not limited to each of the above embodiments. Various changes that can be understood by those skilled in the art can be made to the configuration and details of the present invention. Further, the present invention includes a combination of some or all of the configurations of the above-described embodiments as appropriate.
例えば、各実施形態では全面貼り合せ用のOCRとしてUV硬化型の場合を説明したが、これに限らず、熱硬化型や湿気硬化型、又はこれらの複合硬化型等の場合であっても同様の効果が得られる。また、本発明の技術的効果を損なわない範囲内であれば、ダム材として前記ベゼルと表示パネルの間の間隙を充填するシリコーン樹脂部材の外側にさらなるダム材を設けて同間隙の一部又は全部を塞ぐ構造を採ることを妨げるものではない。たとえば、意匠上ベゼルの一部に特殊な形状を採用し、上記の方法をもってしても間隙を完全に塞ぐことができない場合などには、ピンポイントで当該箇所にダム材である硬化性樹脂組成物を注入してもよい。 For example, in each embodiment, the UV curable case has been described as the OCR for whole surface bonding. However, the present invention is not limited to this, and the same applies to the case of a thermosetting type, a moisture curable type, or a composite curable type thereof. The effect is obtained. Further, as long as the technical effect of the present invention is not impaired, a further dam material is provided outside the silicone resin member that fills the gap between the bezel and the display panel as a dam material, and a part of the gap or It does not preclude taking a structure that covers everything. For example, if the design uses a special shape for a part of the bezel and the gap cannot be completely closed even if the above method is used, the curable resin composition that is a dam material at the point is pinpointed. Things may be injected.
さらにまた、前面パネルの形状は四角形状の場合について説明したが、四角形である必要はなく、任意の多角形、曲線部を有する平板、あるいはこれらの組み合わせであってもよく、更には立体形状であっても構わない。 Furthermore, although the case where the shape of the front panel is a square shape has been described, it is not necessary to be a square shape, it may be any polygonal shape, a flat plate having a curved portion, or a combination thereof, and moreover, it is a three-dimensional shape. It does not matter.
以下、本発明の表示装置の製造方法を実施例および比較例により詳細に説明する。但し本発明は以下の実施例の記載に限定されない。また、下記の実施例により製造された表示装置は本発明の範囲に包含されるものであるが、本発明の表示装置も、以下の実施例の記載に限定されない。 Hereinafter, the manufacturing method of the display apparatus of this invention is demonstrated in detail by an Example and a comparative example. However, the present invention is not limited to the description of the following examples. In addition, display devices manufactured according to the following embodiments are included in the scope of the present invention, but the display devices of the present invention are not limited to the description of the following embodiments.
[各成分]
実施例および比較例には、以下の成分を用い、表1および表2に組成物の組成を示した。
・(a1-1-1)~(a1-1-7)Vi両末端シロキサン(n=X): 分子鎖両末端ジメチルビニルシロキシ基封鎖ジメチルポリシロキサンであり、ジメチルポリシロキサン単位(D単位:(CH3)2SiO2/2で表されるシロキサン単位)の数がXであるもの(本実施例等では、n=37, 272, 382, 400, 404, 460および660であるものを用いており、下記構造式で表される:
(CH2=CH) (CH3)2SiO-((CH3)2SiO)X-Si(CH3)2(CH=CH2))
・(a1-2) MViMQレジン:
構造式{(CH2=CH)(CH3)2SiO1/2}4.8{(CH3)3SiO1/2}39.2(SiO4/2)56
で表されるオルガノポリシロキサン樹脂
・(a3-1-1) CE-SiHシロキサン:
構造式 H(CH3)2SiO-((CH3)2SiO)20-Si(CH3)2H
で表される末端のみにSiH基を有するオルガノハイドロジェンポリシロキサン
・(a3-1-2) CE-SiHシロキサン:
構造式 H(CH3)2SiO-((C6H5)2SiO)-Si(CH3)2H
で表される末端のみにSiH基を有するオルガノハイドロジェンポリシロキサン
・(a3-2-1) XL-SiHシロキサン:
構造式 (CH3)3SiO-((CH3)2SiO)28(H(CH3)SiO)28-Si(CH3)3
で表される分子鎖側鎖に3個以上のSiH基を有する直鎖状オルガノハイドロジェンポリシロキサン
・(a3-2-2) XL-SiHシロキサン:
構造式 {H(CH3)2SiO1/2}60{(C6H5)SiO3/2}40
で表される分子内に3個以上のSiH基を有する樹脂状オルガノハイドロジェンポリシロキサン
・(b1-1-1) Pt: 白金の1,3-ジビニル-1,1,3,3-テトラメチルジシロキサン錯体 (25℃においてヒドロシリル化反応を進行させる硬化反応触媒であり、白金のアルケニルシロキサン錯体)
・(b1-2-1) UV-Pt: (メチルシクロペンタジエニル)トリメチル白金(IV)錯体 (紫外線(UV)照射によりヒドロシリル化反応を進行させる硬化反応触媒)
[Each component]
In the examples and comparative examples, the following components were used, and the compositions of the compositions are shown in Tables 1 and 2.
(A1-1-1) to (a1-1-7) Vi both-end siloxane (n = X): dimethylpolysiloxane blocked with dimethylvinylsiloxy group at both ends of molecular chain, dimethylpolysiloxane unit (D unit: ( (The siloxane unit represented by CH 3 ) 2 SiO 2/2 ) is X (in this example, n = 37, 272, 382, 400, 404, 460 and 660 are used) And is represented by the following structural formula:
(CH 2 = CH) (CH 3 ) 2 SiO-((CH 3 ) 2 SiO) X -Si (CH 3 ) 2 (CH = CH 2 ))
・ (A1-2) M Vi MQ resin:
Structural formula {(CH 2 = CH) (CH 3 ) 2 SiO 1/2 } 4.8 {(CH 3 ) 3 SiO 1/2 } 39.2 (SiO 4/2 ) 56
Organopolysiloxane resin represented by
(A3-1-1) CE-SiH siloxane:
Structural formula H (CH 3 ) 2 SiO-((CH 3 ) 2 SiO) 20 -Si (CH 3 ) 2 H
Organohydrogenpolysiloxane having SiH groups only at the ends represented by
(A3-1-2) CE-SiH siloxane:
Structural formula H (CH 3 ) 2 SiO-((C 6 H 5 ) 2 SiO) -Si (CH 3 ) 2 H
Organohydrogenpolysiloxane having SiH groups only at the ends represented by
(A3-2-1) XL-SiH siloxane:
Structural formula (CH 3 ) 3 SiO-((CH 3 ) 2 SiO) 28 (H (CH 3 ) SiO) 28 -Si (CH 3 ) 3
Linear organohydrogenpolysiloxane having 3 or more SiH groups in the side chain
(A3-2-2) XL-SiH siloxane:
Structural formula {H (CH 3 ) 2 SiO 1/2 } 60 {(C 6 H 5 ) SiO 3/2 } 40
Resinous organohydrogenpolysiloxane having 3 or more SiH groups in the molecule represented by
(B1-1-1) Pt: 1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex of platinum (a curing reaction catalyst for proceeding hydrosilylation reaction at 25 ° C., platinum alkenyl Siloxane complex)
・ (B1-2-1) UV-Pt: (Methylcyclopentadienyl) trimethylplatinum (IV) complex (Curing reaction catalyst that promotes hydrosilylation reaction by ultraviolet (UV) irradiation)
[実施例1~9、比較例1~9の表示装置用のギャップシール剤組成物]
表1および表2に示す組成で各成分をスタティックミキサを用いて均一に混合し、実施例および比較例にかかる組成物を調製した。成分(B)の硬化反応触媒を除き、表中の各成分の数字は質量部である。表中には、さらに、以下の値および測定結果を記載した。
・SiH(CE)/Vi:分子鎖末端のみに珪素結合水素原子を有する直鎖状または分岐鎖状のオルガノハイドロジェンポリシロキサンについて、他の成分中のビニル基の合計1モルに対して珪素結合水素原子のモル数
・SiH(XL)/Vi:分子内に少なくとも3個の珪素結合水素原子を有する直鎖状または樹脂状のオルガノハイドロジェンポリシロキサンついて、他の成分中のビニル基の合計1モルに対して珪素結合水素原子のモル数
・Pt(ppm):白金のアルケニルシロキサン錯体に由来する白金含有量
・UV-Pt(ppm):(メチルシクロペンタジエニル)トリメチル白金(IV)錯体に由来する白金含有量
・初期粘度:組成物の調製直後に、25℃において、TAインスツルメンツ社製レオメーター(AR550)を用いて測定した初期粘度(mPa・s)である。ジオメトリーとして、直径20mmのプレートを用いた。なお、粘度は、シェアレイト20(1/s)における値とした。
・2倍粘度到達時間:組成物の調製直後から、25℃において、TAインスツルメンツ社製レオメーター(AR550)を用いて、1分毎に粘度を測定し、初期粘度の2倍に達した時間(分)を記録した。なお、粘度は、シェアレイト20(1/s)における値とした。
・針入度:2時間以上経過し、硬化反応が事実上完結した後、硬化後のシリコーン樹脂部材について、25℃において、離合社製PENETROMETER RPM-101を用いて、そのJIS K2220で規定される針入度を測定した。
・G’1000Pa到達時間: 組成物の調製直後から、25℃において、TAインスツルメンツ社製レオメーター(AR550)を用いて、ジオメトリーとして、直径20mmのコーンプレートを用い、振動数1Hzの条件で、1分毎に貯蔵弾性率G’を測定し、反応物のG’が1000Paに達した時間(分)を記録した。なお、紫外線照射がある場合(光照射あり)の場合も、同様に測定を行った。
・30分後の流動性の有無:
各組成物を室温下でスタティックミキサで均一に混合した直後に水平な板状に吐出し、25℃において、30分静置した後、当該板を傾けることで流動性の有無を確認した。板を傾けても全く流動が観察されない場合、「非流動性」と評価した。
・光照射あり、20分後の流動性の有無:
各組成物を室温下でスタティックミキサで均一に混合した直後に水平な板状に吐出し、25℃において、オゾンの発生を抑えるためのガラスフィルターを有する2W高圧水銀灯を用いて、365nmでの紫外線照射量が5000mJ/cm2となるように紫外線を照射し、20分静置した後、当該板を傾けることで流動性の有無を確認した。板を傾けても全く流動が観察されない場合、「非流動性」と評価した。
・剪断接着力(MPa)および剪断接着伸び率(%)
実施例1~6については、さらに、以下の方法で剪断接着力(MPa)および剪断接着伸び率(%)を測定し、表1に示した。
測定方法:各組成物を硬化させてなる試料厚さ200μmの表示装置用ギャップシール剤(硬化物)を2枚のガラスプレート間において25mm×25mmの正方形となる範囲で張り合わせ、両側から万能材料試験機(島津製作所製 オートグラフ AGS-1kNG)を用いて、試験速度100mm/分で水平方向に引っ張ることで剪断接着力(MPa)のピーク値を測定し、表1に記載した。さらに、同試験における剪断接着力(MPa)のピーク値における水平方向の変位量を同試料厚さ(200μm)で割った値に100を乗じたものを、剪断接着伸び率(%)として表1に記載した。
[Gap sealant compositions for display devices of Examples 1 to 9 and Comparative Examples 1 to 9]
Each component was uniformly mixed with the composition shown in Table 1 and Table 2 using the static mixer, and the composition concerning an Example and a comparative example was prepared. Except for the curing reaction catalyst of component (B), the number of each component in the table is part by mass. In the table, the following values and measurement results were further described.
SiH (CE) / Vi: For a linear or branched organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the end of the molecular chain, a silicon bond with respect to a total of 1 mole of vinyl groups in other components Moles of hydrogen atoms
SiH (XL) / Vi: For a linear or resinous organohydrogenpolysiloxane having at least three silicon-bonded hydrogen atoms in the molecule, silicon is added to a total of 1 mol of vinyl groups in other components. Number of moles of bonded hydrogen atoms
Pt (ppm): platinum content derived from platinum alkenylsiloxane complex
UV-Pt (ppm): platinum content derived from (methylcyclopentadienyl) trimethylplatinum (IV) complex
Initial viscosity: The initial viscosity (mPa · s) measured immediately after the composition was prepared at 25 ° C. using a TA Instruments rheometer (AR550). A 20 mm diameter plate was used as the geometry. The viscosity was a value at Shearrate 20 (1 / s).
・ Double viscosity arrival time: Immediately after the preparation of the composition, at 25 ° C., the viscosity was measured every minute using a TA Instruments rheometer (AR550), and the time when it reached twice the initial viscosity ( Minutes). The viscosity was a value at Shearrate 20 (1 / s).
・ Penetration: After 2 hours or more have passed and the curing reaction is practically complete, the cured silicone resin member is defined in JIS K2220 at 25 ° C. using PENETROMETER RPM-101 manufactured by Kouaisha. The penetration was measured.
G'1000 Pa arrival time: Immediately after the preparation of the composition, using a rheometer manufactured by TA Instruments (AR550) at 25 ° C., using a cone plate with a diameter of 20 mm as a geometry, and a frequency of 1 Hz, 1 The storage elastic modulus G ′ was measured every minute, and the time (minute) at which G ′ of the reaction product reached 1000 Pa was recorded. In addition, the measurement was performed in the same manner when there was ultraviolet irradiation (with light irradiation).
・ Check for fluidity after 30 minutes:
Immediately after each composition was uniformly mixed with a static mixer at room temperature, it was discharged into a horizontal plate shape, allowed to stand at 25 ° C. for 30 minutes, and then tilted to confirm the presence or absence of fluidity. If no flow was observed even when the plate was tilted, it was evaluated as “non-flowable”.
-With light irradiation, fluidity after 20 minutes:
Each composition was uniformly mixed with a static mixer at room temperature, and then discharged into a horizontal plate shape. At 25 ° C., ultraviolet rays at 365 nm were used using a 2 W high-pressure mercury lamp having a glass filter for suppressing ozone generation. Ultraviolet rays were irradiated so that the irradiation amount was 5000 mJ / cm 2, and after standing for 20 minutes, the presence or absence of fluidity was confirmed by tilting the plate. If no flow was observed even when the plate was tilted, it was evaluated as “non-flowable”.
-Shear adhesive force (MPa) and shear bond elongation (%)
For Examples 1 to 6, the shear adhesive force (MPa) and the shear adhesive elongation (%) were further measured by the following methods, and are shown in Table 1.
Measurement method: Gap sealant for display device (cured product) with a sample thickness of 200 μm obtained by curing each composition is bonded in a range of 25 mm × 25 mm square between two glass plates, and a universal material test from both sides Using a machine (manufactured by Shimadzu Corp., Autograph AGS-1kNG), the peak value of the shear adhesive strength (MPa) was measured by pulling in the horizontal direction at a test speed of 100 mm / min. Further, the value obtained by multiplying the horizontal displacement at the peak value of the shear adhesive force (MPa) in the same test by the sample thickness (200 μm) multiplied by 100 is shown in Table 1 as the shear adhesive elongation (%). It was described in.
実施例1~9と対応する比較例1~9は、ヒドロシリル化反応触媒の含有量、特に25℃でヒドロシリル化反応活性を有する(b1-1-1)成分の含有量が相違する。白金量の多い、実施例においては、混合直後においては、初期粘度1100~21000mPasの範囲の液状組成物であり、初期粘度の2倍に到達するまでの時間が3~14分の範囲内であるので、十分な可使時間を有する一方、30分以内に非流動性の反応物を与えるものであった。また、光活性の白金触媒を含む実施例5~7、9にあっては、紫外線の照射を併用することで、より迅速な硬化反応を実現し、20分以内に非流動性の反応物を与えるものであった。一方、比較例においては、25℃では30分後も流動性であり、初期粘度の2倍に達するまでの時間も18分以上と硬化速度が遅く、本発明の表示装置用のギャップシール剤組成物として用いると、目張りが不十分となったり、空隙から流出して表示モジュール内にしみ込むことが懸念される。 The comparative examples 1 to 9 corresponding to the examples 1 to 9 differ in the content of the hydrosilylation reaction catalyst, particularly the content of the component (b1-1-1) having hydrosilylation reaction activity at 25 ° C. In Examples where the amount of platinum is large, immediately after mixing, it is a liquid composition having an initial viscosity in the range of 1100 to 21000 mPas, and the time to reach twice the initial viscosity is in the range of 3 to 14 minutes. Therefore, while having a sufficient pot life, a non-flowable reactant was given within 30 minutes. In Examples 5 to 7 and 9 containing a photoactive platinum catalyst, a more rapid curing reaction was realized by using ultraviolet irradiation together, and a non-flowable reactant was formed within 20 minutes. It was to give. On the other hand, in the comparative example, at 25 ° C., it is fluid after 30 minutes, and the time until it reaches twice the initial viscosity is 18 minutes or more. When used as an object, there is a concern that the weathering will be insufficient or that it will flow out of the gap and penetrate into the display module.
[表示装置の貼り合わせモデル試験]
表示装置の貼り合せ品質を評価するために、以下のようなモデル試験を行った。
表示部を模した50mm x 50mm x 1mm のガラス板(A)、ベゼルを模した、中央部に 40mm x 40mm の切り抜き部分を持つ 55mm x 55mm x 1mm のアクリル製フレーム(B)、及び前面パネルを模した 55mm x 55mm x 1mm のガラス板(C)。表示部 A の四隅に、ベゼル B との間隙を持たせるための1.7mm 高のスペーサーを配置し、ベゼル B を実施例、比較例の方法によって表示部 A に接着・硬化。後に、表示部 A とベゼル B の中央部に形成される空間にOCRを充填し、前面パネル C を貼り合せる。充填したOCRが、前面パネル C 貼り合せ時に、表示部 A とベゼル B 間の間隙より漏洩するかどうか等を観測することによって、ベゼル B の接合品質(シール不良なく、ベゼル B の全周に亘って隙間無く表示部 A と接合できている)を評価した。
なお、なお、上記の実施例5の表示装置用ギャップシール剤組成物を、本発明の実施例11に用いたが、他の実施例1~4,6~9の組成物であっても同様に利用可能である。
[Bonding model test of display device]
In order to evaluate the bonding quality of the display device, the following model test was performed.
A glass plate (A) of 50mm x 50mm x 1mm that imitates the display part, a 55mm x 55mm x 1mm acrylic frame (B) that has a cutout part of 40mm x 40mm in the center imitating the bezel, and the front panel Simulated glass plate (C) of 55 mm x 55 mm x 1 mm. 1.7 mm high spacers are provided at the four corners of the display part A to provide a gap with the bezel B, and the bezel B is adhered and cured to the display part A by the method of the example and the comparative example. Later, OCR is filled in the space formed in the central part of the display part A and the bezel B, and the front panel C is bonded. By observing whether the filled OCR leaks from the gap between the display A and the bezel B when the front panel C is bonded, the bonding quality of the bezel B (without seal failure, over the entire circumference of the bezel B) And the display part A can be joined without any gaps).
Note that the gap sealant composition for display device of Example 5 was used in Example 11 of the present invention, but the same applies to the compositions of other Examples 1 to 4, 6 to 9. Is available.
[実施例10]
上記の実施例5の表示装置用ギャップシール剤組成物(以下、「UV硬化性接着剤」という)をスタティックミキサで混合しながら、武蔵クリアシリンジ PSY-10E へ充填し、オートディスペンサ(武蔵エンジニアリング株式会社製 SHOTMASTER 300 DS-S)へセットし、18G 標準ニードルを装着した。
[Example 10]
The above-mentioned gap sealant composition for display device of Example 5 (hereinafter referred to as “UV curable adhesive”) was mixed into a Musashi clear syringe PSY-10E while mixing with a static mixer, and an auto dispenser (Musashi Engineering Co., Ltd.). Set to company SHOTMASTER 300 DS-S) and fitted with 18G standard needle.
表示部 A の四隅(頂点より各辺から7mmづつ内側)へ、吐出圧 500kPa で1秒づつ UV硬化性接着剤を吐出し、UV硬化性接着剤を配置し、ベゼル B を、表示部 A に対して、中央揃えで貼り合せた。このとき、各点(四隅)において、表示部AとベゼルBの間隙は、UV硬化性接着剤によって表示部Aに対して垂直方向に充填されていた。 Dispense UV curable adhesive into the four corners of the display area A (inside from the apex, 7mm from each side) at a discharge pressure of 500kPa for 1 second, place the UV curable adhesive and place the bezel B on the display area A On the other hand, it was pasted with center alignment. At this time, at each point (four corners), the gap between the display portion A and the bezel B was filled in a direction perpendicular to the display portion A with a UV curable adhesive.
ニードルをL字ニードル(武蔵カーブニードル CPN-18G-A90)に換え、ニードルの先端が、表示部 A とベゼル B の間隙間に1mm以上侵入した位置に設定し、吐出圧 500kPa、塗布速度 1.8mm/s で、先に四隅に配置したUV硬化性接着剤を塗布の起点/終点として各点を繋ぐように、四辺に UV硬化性接着剤を塗布し、365nm UV を2J 照射して接着剤を硬化、ベゼル B を表示部 A に接合した。 Change the needle to an L-shaped needle (Musashi curve needle CPN-18G-A90), and set the tip of the needle to a position where it has entered 1 mm or more into the gap between display part A and bezel B, discharge pressure 500kPa, coating speed 1. At 8mm / s, apply UV curable adhesive on the four sides so that the UV curable adhesive placed at the four corners as the starting point / end point of the application is connected, and irradiate 365nm UV with 2J. The bezel B was joined to the display part A.
表示部 A とベゼル B で形成される中央部の空間に、OCR(東レ・ダウコーニング製 EG-1200)をスタティックミキサで混合しながら 5g 充填し、前面パネル C を表示部 A とベゼル B の接合体に対して平行に、気泡を含まないよう中心揃えで徐々に貼り合せて行き、ベゼル B と前面パネル C の接合境界から、OCR が漏洩する寸前まで、前面パネル C をベゼル B へ加圧接合し、室温で30分放置して OCR を硬化させた。 Fill the center space formed by the display unit A and the bezel B with 5g while mixing OCR (Toray Dow Corning EG-1200) with a static mixer, and join the front panel C with the display unit A and the bezel B Gently pasting with the center aligned so that it does not contain air bubbles parallel to the body, press the front panel C to the bezel B か ら from the boundary of the bezel B and the front panel C 寸 until just before the OCR 漏洩 leaks And left at room temperature for 30 minutes to cure the OCR.
表示部 A とベゼル B の間隙を全周検査すると、OCR の漏洩は全く観測されなかった。 When the entire gap between the display area A and bezel B was inspected, no leakage of OCR was observed.
[参考例1]
表示部 A の四隅へのUV硬化性接着剤の事前塗布を行わず、18G 標準ニードルの先端をベゼル B 中央切抜き部内辺に接触しない位置に設定し、吐出圧 500kPa、塗布速度 1.8mm/s で、中央切抜き部四辺に UV硬化性接着剤を塗布し、365nm UV を2J 照射して接着剤を硬化、ベゼル B を表示部 A に接合した他は実施例1と同様にして、前面パネル C をベゼル B へ加圧接合し、室温で30分放置して OCR を硬化させた。なお、比較例1において、UV硬化性接着剤は表示部AとベゼルBの間隙に対して垂直方向から塗布されている。
[Reference Example 1]
Without pre-applying UV curable adhesive to the four corners of display A, set the tip of the 18G standard needle so that it does not touch the inner edge of the central cutout of bezel B, discharge pressure 500kPa, application speed 1.8mm / s In the same manner as in Example 1, except that a UV curable adhesive was applied to the four sides of the central cutout, the adhesive was cured by irradiating 365 nm UV at 2 J, and the bezel B was joined to the display A. Was pressure bonded to bezel B and allowed to stand at room temperature for 30 minutes to cure the OCR. In Comparative Example 1, the UV curable adhesive is applied from the direction perpendicular to the gap between the display portion A and the bezel B.
表示部 A とベゼル B の間隙から、OCR の漏洩が観測された。 Leakage of OCR was observed from the gap between the display area (A) and the bezel (B).
[参考例2]
表示部 A の四隅へのUV硬化性接着剤の事前塗布を行わず、18G 標準ニードルの先端をベゼル B 中央切抜き部内辺に接触しない位置に設定し、吐出圧 500kPa、塗布速度 0.9mm/s で、中央切抜き部四辺に UV硬化性接着剤を塗布し、365nm UV を2J 照射して接着剤を硬化、ベゼル B を表示部 A に接合した他は実施例1と同様にして、前面パネル C をベゼル B へ加圧接合し、室温で30分放置して OCR を硬化させた。なお、比較例2において、UV硬化性接着剤は表示部AとベゼルBの間隙に対して垂直方向から塗布されており、実施例10および参考例1に対して1/2の塗布速度を採用して、倍量の塗布を行っている。
[Reference Example 2]
Without pre-applying UV curable adhesive to the four corners of display area A, set the tip of the 18G standard needle so that it does not touch the inner edge of the central cutout of bezel B, discharge pressure 500kPa, application speed 0.9mm / s In the same manner as in Example 1, except that a UV curable adhesive was applied to the four sides of the central cutout, the adhesive was cured by irradiating 365 nm UV at 2 J, and the bezel B was joined to the display A. Was pressure bonded to bezel B and allowed to stand at room temperature for 30 minutes to cure the OCR. In Comparative Example 2, the UV curable adhesive was applied from the direction perpendicular to the gap between the display portion A and the bezel B, and a coating speed of 1/2 was applied to Example 10 and Reference Example 1. Then, double the amount of coating is performed.
表示部 A とベゼル B の間隙から、OCR の漏洩は、観測されなかったが、表示部 A と前面パネル C の貼り合せが非平行となり、ベゼル B と前面パネル C との間隙が、各辺で不均一であった。 No leakage of OCR was observed from the gap between the display unit A and the bezel B, but the bonding between the display unit A and the front panel C became non-parallel, and the gap between the bezel B and the front panel C C It was uneven.
[実験結果の概要]
以下、
・OCR漏洩の有無、
・前面パネルの取り付け精度、すなわち、UV硬化性接着剤の塗布に由来してベゼルと前面パネルの間隙に対する不均一の発生の有無
を実験条件との関係でまとめたものを表3に示す。
[Summary of experimental results]
Less than,
・ OCR leakage,
Table 3 shows the accuracy of mounting the front panel, that is, the presence or absence of non-uniformity in the gap between the bezel and the front panel due to the application of the UV curable adhesive in relation to the experimental conditions.
表3に示す通り、事前にベゼルと表示部の間隙を本発明の表示装置用ギャップシール剤組成物であるUV硬化性接着剤の四点塗布により事前に垂直方向に充填し、かつ、当該塗布により得た接着剤(樹脂部材)を起点/終点として、当該間隙に対してL字型ニードルを用いて間隙に対してUV硬化性接着剤を水平方向から定速で注入した実施例10においては、OCRの漏洩も、前面パネルの取り付け不良も発生せず、信頼性に優れた表示装置が製造可能であることがモデル試験で証明された。 As shown in Table 3, the gap between the bezel and the display portion is previously filled in the vertical direction by four-point application of the UV curable adhesive which is the gap sealant composition for display device of the present invention, and the application is performed. In Example 10 in which a UV curable adhesive was injected at a constant speed from the horizontal direction into the gap using an L-shaped needle with respect to the gap, starting from the adhesive (resin member) obtained by The model test proved that it is possible to manufacture a display device with excellent reliability without causing leakage of the OCR and poor mounting of the front panel.
一方、公知技術を用いて間隙に対してUV硬化性接着剤を間隙に対して垂直方向から注入して間隙を塞ごうとした場合、参考例1のように少量塗布ではOCRの漏洩を防止できず、目張りが不十分となる。一方、参考例2のように大量塗布すると、UV硬化性接着剤に由来して、部材間の取り付け不良が発生するほか、ベゼル周囲に大量のUV硬化性接着剤が存在するため、端部における表示ムラ等の問題の発生も懸念される。 On the other hand, when a UV curable adhesive is injected into the gap from a direction perpendicular to the gap by using a known technique, the leakage of OCR can be prevented by applying a small amount as in Reference Example 1. Therefore, the weathering is insufficient. On the other hand, when a large amount of coating is applied as in Reference Example 2, a defect in attachment between members occurs due to the UV curable adhesive, and a large amount of UV curable adhesive exists around the bezel. There is also concern about the occurrence of problems such as display unevenness.
本発明は、液晶ディスプレイに限らず、例えば有機ELディスプレイ、電子ペーパーディスプレイ、プラズマディスプレイ等、表示ディスプレイ分野全般に利用可能である。 The present invention is not limited to liquid crystal displays, and can be used in the field of display displays such as organic EL displays, electronic paper displays, plasma displays, and the like.
<実施形態>
101~110 表示装置
10 表示パネル
11 表示面
12 偏光板
13 CF基板
14 TFT基板
15 偏光板
16 遮光膜
17 FPC基板
18 表示領域
20 ベゼル
21 枠部
22 開口端
23 表面
30 前面パネル(タッチパネル)
31 カバーパネル
32 センサガラス
33 FPC基板
40~42 樹脂部材
50 OCR(光学弾性樹脂)
60 接着部材
70 表示モジュール
71 バックライトユニット
72 間隙
91 L字ノズルを備えたディスペンサ装置
94 ノズル
<Embodiment>
101 to 110
31
60
Claims (16)
および
(B)硬化反応触媒
を含有してなり、25℃における初期粘度が100~100000mPa・s の範囲の液状であり、さらに、同温度下で少なくとも30分以内に非流動性の反応物を形成することを特徴とする表示装置用のギャップシール剤組成物。 (A) one or more types of organopolysiloxane having a curing reactive functional group in the molecule;
And (B) a liquid containing a curing reaction catalyst and having an initial viscosity at 25 ° C. in the range of 100 to 100,000 mPa · s, and forming a non-flowable reactant within at least 30 minutes at the same temperature. A gap sealant composition for a display device.
(A1)炭素-炭素二重結合を含む硬化反応性基を有するオルガノポリシロキサン、および
(A3)珪素原子結合水素原子を有するオルガノハイドロジェンポリシロキサンを少なくとも含み、
成分(B)が、
(B1)ヒドロシリル化反応触媒を少なくとも含み、
組成物中の炭素-炭素二重結合1モルに対して、珪素結合水素原子が0.1~10モルの範囲にあることを特徴とする、請求項1または請求項2に記載の表示装置用のギャップシール剤組成物。 Component (A) is
(A1) at least an organopolysiloxane having a curing reactive group containing a carbon-carbon double bond, and (A3) an organohydrogenpolysiloxane having a silicon atom-bonded hydrogen atom,
Component (B) is
(B1) at least a hydrosilylation reaction catalyst,
3. The display device according to claim 1, wherein the silicon-bonded hydrogen atom is in the range of 0.1 to 10 moles per mole of the carbon-carbon double bond in the composition. Gap sealant composition.
(B1-1)高エネルギー線の照射なしで、組成物中で活性を示す第一のヒドロシリル化反応触媒、及び
(B1-2)高エネルギー線の照射がないと活性を示さないが、高エネルギー線の照射により組成物中で活性を示す第二のヒドロシリル化反応触媒
を含む硬化反応触媒であり、成分(B1-1)と成分(B1-2)の質量比が90/10~5/95の範囲であり、
組成物を調製した直後に高エネルギー線を照射した場合、25℃で少なくとも20分以内に非流動性の反応物を形成する特徴をさらに有する、
請求項1~3のいずれか1項に記載の表示装置用のギャップシール剤組成物。 Component (B) is
(B1-1) a first hydrosilylation reaction catalyst that shows activity in the composition without irradiation with high energy rays, and (B1-2) that does not show activity without irradiation with high energy rays, but has high energy A curing reaction catalyst comprising a second hydrosilylation reaction catalyst that is active in the composition upon irradiation with a ray, wherein the mass ratio of component (B1-1) to component (B1-2) is 90/10 to 5/95 Range of
When irradiated with high energy rays immediately after preparing the composition, it further has the characteristic of forming a non-flowable reactant within at least 20 minutes at 25 ° C.
The gap sealant composition for a display device according to any one of claims 1 to 3.
(A1-1)分子鎖末端のみにアルケニル基を有する直鎖状または分岐鎖状のオルガノポリシロキサン 100質量部、
(A1-2)分子内に少なくとも1つの分岐シロキサン単位を有し、ビニル(CH2=CH―)基の含有量が1.0~5.0質量%の範囲内にあるアルケニル基含有オルガノポリシロキサン樹脂 0~20質量部、
(A3-1)分子鎖末端のみに珪素結合水素原子を有する直鎖状または分岐鎖状のオルガノハイドロジェンポリシロキサン 成分(A1-1)および(A1-2)中のビニル基の合計1モルに対して珪素結合水素原子が0.1~10モルとなる量、および
(A3-2)分子内に少なくとも3個の珪素結合水素原子を有する直鎖状または樹脂状のオルガノハイドロジェンポリシロキサン 成分(A1-1)および(A1-2)中のビニル基の合計1モルに対して珪素結合水素原子が0~1モルとなる量
を含有するオルガノポリシロキサンであることを特徴とする、請求項1~4のいずれか1項に記載の表示装置用のギャップシール剤組成物。 Component (A) is
(A1-1) 100 parts by mass of a linear or branched organopolysiloxane having an alkenyl group only at the molecular chain end,
(A1-2) An alkenyl group-containing organopolysiloxane having at least one branched siloxane unit in the molecule and having a vinyl (CH2═CH—) group content in the range of 1.0 to 5.0 mass% 0-20 parts by mass of resin,
(A3-1) A linear or branched organohydrogenpolysiloxane having a silicon-bonded hydrogen atom only at the molecular chain terminal, in a total of 1 mole of vinyl groups in the components (A1-1) and (A1-2) (A3-2) a linear or resinous organohydrogenpolysiloxane component having at least three silicon-bonded hydrogen atoms in the molecule (A3-2) 2. An organopolysiloxane containing an amount of 0 to 1 mole of silicon-bonded hydrogen atoms relative to a total of 1 mole of vinyl groups in A1-1) and (A1-2). 5. The gap sealant composition for a display device according to any one of items 1 to 4.
(B1-1-1)白金のアルケニルシロキサン錯体、及び
(B1-2-1)(置換および非置換シクロペンタジエニル)トリメチル白金(IV)、βージケトナートトリメチル白金(IV)、ビス(β―ジケトナート)白金(II)から選択される少なくとも1つを含む硬化反応触媒であり、あり、(B1-1-1)成分と(B1-2-1)成分の質量比が90/10~5/95の範囲である、請求項1~5のいずれか1項に記載の表示装置用のギャップシール剤組成物。 Component (B) is
(B1-1-1) an alkenylsiloxane complex of platinum, and (B1-2-1) (substituted and unsubstituted cyclopentadienyl) trimethylplatinum (IV), β-diketonatotrimethylplatinum (IV), bis ( β-diketonate) a curing reaction catalyst containing at least one selected from platinum (II), wherein the mass ratio of the component (B1-1-1) to the component (B1-2-1) is from 90/10 to The gap sealant composition for a display device according to any one of claims 1 to 5, which is in the range of 5/95.
成分(B)が、(B2)縮合反応触媒を含有することを特徴とする、
請求項1~6のいずれか1項に記載の表示装置用のギャップシール剤組成物。 Component (A) is (A2-1) an organopolysiloxane containing one or more organopolysiloxanes having a condensation reactive group selected from a hydroxyl group, an alkoxy group, an acyloxy group, and an oximoxy group only at the molecular chain end. Siloxane,
Component (B) contains (B2) a condensation reaction catalyst,
The gap sealant composition for a display device according to any one of claims 1 to 6.
前記ベゼルの前記開口部の全周の少なくとも一部または全部において、前記ベゼルと表示パネルの間の空隙を、当該空隙に対する注入角が、水平~75度の範囲となる角度で
請求項1~13のいずれか1項に記載の表示装置用のギャップシール剤組成物を注入して充填する工程
を含むことを特徴とする表示装置の製造方法。 A display device having a display panel having a display surface, and a bezel having a frame portion and an opening end inside the frame portion and covering the display surface side periphery of the display panel with the frame portion is manufactured. A method,
The gap between the bezel and the display panel is formed at an angle at which an injection angle with respect to the gap is in a range of horizontal to 75 degrees in at least a part or all of the entire circumference of the opening of the bezel. A method for manufacturing a display device, comprising a step of injecting and filling the gap sealant composition for a display device according to any one of the above.
枠部と当該枠部の内側の開口端とを有し、前記表示パネルの前記表示面側の周縁を前記枠部で覆うベゼルと、
前記ベゼルの前記開口部の全周の少なくとも一部または全部において、前記ベゼルと表示パネルの間の空隙が請求項1~13のいずれか1項に記載の表示装置用のギャップシール剤組成物を硬化させてなる樹脂部材により充填された構造を有する表示装置。 A display panel having a display surface;
A bezel having a frame portion and an opening end inside the frame portion, and covering the periphery of the display panel side of the display panel with the frame portion;
The gap sealant composition for a display device according to any one of claims 1 to 13, wherein a gap between the bezel and the display panel is provided on at least a part or all of the entire circumference of the opening of the bezel. A display device having a structure filled with a cured resin member.
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| JP2020515594A JP7316267B2 (en) | 2018-04-27 | 2019-04-26 | GAP SEALING COMPOSITION FOR DISPLAY DEVICE, METHOD FOR MANUFACTURING DISPLAY DEVICE USING SAME, AND DISPLAY DEVICE |
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| JP2018086178 | 2018-04-27 | ||
| JP2018-086178 | 2018-04-27 |
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| PCT/JP2019/017859 Ceased WO2019208756A1 (en) | 2018-04-27 | 2019-04-26 | Gap sealant composition for display device, and method for manufacturing display device and display device using same |
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| JP (1) | JP7316267B2 (en) |
| TW (1) | TW201945508A (en) |
| WO (1) | WO2019208756A1 (en) |
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| JPWO2019208756A1 (en) | 2021-05-13 |
| JP7316267B2 (en) | 2023-07-27 |
| TW201945508A (en) | 2019-12-01 |
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