JP2014199346A - Image display device manufacturing method and image display device - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an image display device having a designable area with good appearance quality produced using a photocurable liquid composition, which is photo-cured simply and quickly even when located in hidden dark areas, for bonding an image display module and a light-transmissive cover board.SOLUTION: An image display device manufacturing method involves; preparing a curable composition (I) 8 containing a polymerizable compound (A) having one or more carbon-carbon double bonds, a photopolymerization initiator (B), and an organic peroxide (C) and a curable composition (II) containing the compound (A), a photopolymerization initiator (B), a fourth period transition metal element compound (D), and a reductant (E); applying the curable composition (I) 8 and the curable composition (II) on a light-transmissive protection cover board and an image display module such that the two compositions do not come into contact with each other; half-curing the curable composition (II) by light irradiation; bringing the curable composition (I) 8 and the curable composition (II) into contact with each other by putting the light-transmissive protection cover board and the image display module together; and then irradiating the compositions with light.

Description

  The present invention relates to a method for manufacturing an image display device using a two-component curable composition comprising two types of curable compositions (I) and (II), an image display device, and an electric / electronic device equipped with the image display device.

  For liquid crystal modules and organic EL modules used for image display such as mobile phones, smartphones, and tablets, a transparent protective cover is placed on the forefront of these modules, and an air layer is provided between the module and the protective cover. Yes. With this structure, even if these image display devices are subjected to a physical impact due to dropping or the like, they are less susceptible to impact such as damage to the module.

  In recent years, from the viewpoint of improving the visibility of these image display devices and imparting impact resistance, a conventional method of filling an air layer with a curable resin composition curable with light has been used.

  However, UV light, which is the trigger for curing, has become more complex due to the complexity of the design of the outermost protective cover for the purpose of providing design to mobile phones and touch panels, as represented by the touch sensor panel with integrated surface protective cover. There is an inconvenience that the area where the light does not permeate increases and an unreacted part is formed. As a specific example of the defective part, when the image display module such as a liquid crystal display or an organic EL display is bonded to the protective cover or the touch panel, or the protective cover and the touch panel are bonded, the periphery of the protective cover is applied for decoration purposes. Image display module made of a photo-curable composition, such as a black frame (black matrix), a touch panel electrode, a flexible printed circuit board (FPC) connected to an image display module, or the like (dark part) below a portion that does not transmit light In pasting, there was a problem that unreacted liquid composition remained in the dark part and leaked, causing contamination of the image display module.

  As a countermeasure, for example, a method of completely curing in a heated atmosphere after UV irradiation by adding a thermal polymerization initiator in addition to an initiator for UV curing has been proposed. However, although this improvement method can secure the curability in the dark part, the constituent members of the image display module and the protective cover may be deformed by heating, and the applicable range is limited, and the heat curing requires a long time. Overheating is indispensable, and improvement in productivity is also necessary.

  As another countermeasure, there is a technique using a UV curing initiator and a redox type curing initiator in combination (Patent Documents 1 to 4). For example, an organic peroxide is used as the redox type curing initiator, and a reducing polymerization accelerator such as a transition metal compound or amine is added to the system as a curing reaction accelerator, so that the reaction can be carried out quickly even at room temperature. There is a method to start and redox cure the dark part. Usually, a method is used in which a composition component containing a peroxide and a composition component containing a curing reaction accelerator are prepared separately, and both are mixed and supplied to the necessary location immediately before curing. The advantage of this method is that the curing time can be arbitrarily adjusted by combining a suitable organic oxide and a curing reaction accelerator, but the cured product obtained by redox curing often exhibits strong coloration or whitening. In addition, there is a problem that it is practically impossible to use in applications where high quality is required for appearance such as bonding of image display modules, such as further discoloration at high temperatures. Regarding this problem, a first liquid containing a photopolymerization initiator and a peroxide and a second liquid containing a reducing agent capable of decomposing the peroxide are prepared, and the second liquid is applied to a dark part and bonded. A method has been proposed (Patent Document 5). In this method, the visible portion is rapidly cured by light irradiation, and in the dark portion, polymerization is initiated by the decomposition of the peroxide by two-liquid contact, and the dark portion that is not exposed to light can also be cured. However, since the reaction in the dark part is a reaction by contact rather than mixing, the collision frequency of the components involved in the reaction is low, and it takes a relatively long time to completely cure. There was room for room. Also, since the position away from the contact interface is difficult to cure, the uncured component remains, the uncured component leaks to the outside of the module at a high temperature, penetrates into the module, and contaminates the display part. There was still room for further improvement in terms of reliability, such as coloring oozing out into the visual recognition area.

Japanese Patent Laid-Open No. 5-320284 JP 2009-108274 A Japanese Patent Application Laid-Open No. 2009-079204 JP 2006-299257 A JP 2012-219180 A

  The present invention provides two types of curable compositions (I) and (II) for bonding an image display module / translucent protective cover board that can be quickly cured by light and that can be easily and quickly cured even in a dark part. An object of the present invention is to provide an image display device manufacturing method and an image display device with good appearance quality of a design portion by using a two-component curable composition comprising:

As a result of intensive studies to solve the above problems, the present invention has been completed. That is, the present invention
A curable composition (I) containing a compound (A) having one or more polymerizable carbon-carbon double bonds, a photopolymerization initiator (B), and an organic peroxide (C);
A translucent protective cover board using the curable composition (II) containing the compound (A), photopolymerization initiator (B), fourth-period transition metal element compound (D), and reducing agent (E) A method for manufacturing an image display device for bonding an image display module together,
The translucent protective cover board and / or the image display module is coated with the curable composition (II) in a dark portion where light is not transmitted when the translucent protective cover board and the image display module are bonded together. The curable composition (I) is applied to a portion of the protective protective cover board and / or image display module that does not come into contact with the curable composition (II), and the curable composition (II) is temporarily cured by light irradiation. After performing, the translucent protective cover board and the image display apparatus are bonded together, the curable composition (I) is brought into contact with the curable composition (II) that has been temporarily cured, and light irradiation is performed. About.

  It is preferable that (A) component of curable composition (I) and / or curable composition (II) is a polymer or an oligomer.

  The polymer or oligomer of the component (A) is preferably a vinyl polymer.

  (A) Component vinyl polymer is polyisobutylene, hydrogenated polyisoprene, hydrogenated polybutadiene, (meth) acrylic acid monomer, acrylonitrile monomer, aromatic vinyl monomer, fluorine-containing vinyl monomer and silicon-containing It is preferable to select at least one polymer selected from polymers produced mainly by polymerizing monomers selected from the group consisting of vinyl monomers.

The polymerizable carbon-carbon double bond in the component (A) is preferably represented by the general formula (1).
^{-Z-C (= O) -C} (R 1) = CH 2 (1)
(In the formula, R ¹ is hydrogen or a hydrocarbon group having a substituted or unsubstituted linear or branched structure having 1 to 20 carbon atoms, and a part of the hydrocarbon bond is an ether bond, ester bond, amino It may be substituted with a bond, an amide bond, etc. Z is selected from a hetero atom, NR ² (R ² is a hydrogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms). Group.)

  It is preferable that the addition amount of (B) component is 0.025 weight part-3 weight part with respect to 100 weight part of (A) component in curable composition (I) and (II).

  It is preferable that the addition amount of (C) component is 0.1 weight part-2 weight part with respect to 100 weight part of (A) component in curable composition (I).

  It is preferable that (C) component is a hydroperoxide.

  It is preferable that the addition amount of (D) component is 0.5 weight part-2 weight part with respect to 100 weight part of (A) component in curable composition (II).

  The component (D) is preferably at least one selected from vanadium, titanium, chromium, manganese, iron, cobalt, nickel, copper organic acid salts or metal chelate compounds.

  (E) It is preferable that the addition amount of a component is 0.1-15 weight part with respect to 100 weight part of (A) component in curable composition (II).

  The component (E) is preferably selected from at least one selected from tertiary amines, orthobenzoixsulfimides, mercaptans, thiourea compounds, and salts thereof.

  The present invention relates to an image display device manufactured by the above method.

  The present invention relates to an electric / electronic device equipped with the image display device described above.

  According to the present invention, when the air gap existing between the FPD and the front cover board is filled and bonded with the curable resin for the purpose of improving visibility and imparting impact resistance, the FPD and the cover board are bonded together. About the dark part where photocuring of this becomes difficult, another curable composition can be apply | coated before bonding and it can be made to semi-harden by light irradiation, and the flow can be stopped. Thereafter, the dark part can be completely cured by a redox reaction by two-component contact. The image display device manufactured by this method can supply highly reliable products even when the dark area is narrow, because the coloring component derived from the liquid in the dark area and the dark part uncured material are difficult to leak into the outer edge and inside of the FPD. It becomes.

It is a figure which shows apply | coating curable composition (I) and curable composition (II) to a translucent protective cover board, and bonding to a liquid crystal module. It is a figure when light irradiation is performed to curable composition (II) apply | coated to the translucent protective cover board, and curable composition (II) is temporarily hardened | cured. A diagram of the curable compositions (I) and (II) applied to the translucent protective cover board, when only the curable composition (II) is irradiated with light and the curable composition (II) is temporarily cured. It is. It is the figure immediately after bonding a translucent protective cover board and a liquid crystal module. Continuing from FIG. 4, the translucent protective cover board and the liquid crystal module are bonded together, the curable composition (I) spreads wet, reacts with the semi-cured curable composition (II), and reacts. It is a figure when thing (II) hardens | cures. FIG. 6 is a diagram when the light-transmitting protective cover board and the liquid crystal module are bonded together and light irradiation is performed from the light-transmitting protective cover board side, and the curable composition (I) is cured.

The present invention relates to a curable composition (I) containing a compound (A) having one or more polymerizable carbon-carbon double bonds, a photopolymerization initiator (B), an organic peroxide (C),
A translucent protective cover board using the curable composition (II) containing the compound (A), photopolymerization initiator (B), fourth-period transition metal element compound (D), and reducing agent (E) A method for manufacturing an image display device for bonding an image display module together,
When the light-transmitting protective cover board and / or the image display module is bonded to the light-transmitting protective cover board and the image display module, the curable composition (I) is applied to the dark portion where light is not transmitted. The curable composition (I) is applied to a portion of the protective protective cover board and / or image display module that does not come into contact with the curable composition (II), and the curable composition (II) is temporarily cured by light irradiation. After performing, the translucent protective cover board and the image display apparatus are bonded together, the curable composition (I) is brought into contact with the curable composition (II) that has been temporarily cured, and light irradiation is performed. About.

  The present invention will be described in detail below.

<Compound (A)>
The curable composition of the present invention contains a compound (A) having one or more polymerizable carbon-carbon double bonds. The component (A) may contain any of a low molecular weight compound, an oligomer and a polymer, but preferably contains a polymer or oligomer, and more preferably contains a vinyl polymer. The oligomer described here refers to a compound having a repeating unit of an organic compound and comprising 2 to 100 repeating units, and the polymer is a structure having a repeating unit of the compound in the polymer main chain and having a structure of 100 or more. The compound which consists of a repeating unit of. The main chain of the polymer is not particularly limited, but a vinyl polymer is preferable. Examples of the polymer other than the vinyl polymer include polycarbonate, polyester, polyamide, polyoxyalkylene, and polysiloxane.

  Examples of the vinyl polymer include hydrocarbon polymers such as polyisobutylene, hydrogenated polyisoprene, hydrogenated polybutadiene, (meth) acrylic monomers, acrylonitrile monomers, aromatic vinyl monomers, and fluorine-containing vinyls. A polymer produced mainly by polymerizing a monomer selected from the group consisting of a system monomer and a silicon-containing vinyl monomer is preferred. Here, “mainly” means that 50 mol% or more of the monomer units constituting the vinyl polymer is the above monomer, and preferably 70 mol% or more. Furthermore, as the vinyl polymer, a (meth) acrylic polymer produced by mainly polymerizing polyisobutylene and a (meth) acrylic monomer is preferable, and a (meth) acrylic polymer is more preferable. As the (meth) acrylic polymer, an acrylic polymer is preferable, and an acrylic ester polymer produced by mainly polymerizing an acrylic ester monomer is more preferable.

  (Meth) acrylic monomers include: (meth) acrylic acid; methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, (meth) acrylic acid n-butyl, isobutyl (meth) acrylate, tert-butyl (meth) acrylate, n-pentyl (meth) acrylate, n-hexyl (meth) acrylate, cyclohexyl (meth) acrylate, (meth) acrylic acid n-heptyl, n-octyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, nonyl (meth) acrylate, decyl (meth) acrylate, dodecyl (meth) acrylate, phenyl (meth) acrylate, Toluyl (meth) acrylate, benzyl (meth) acrylate, (meth) acrylic acid-2-methoxy ester , 3-methoxybutyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, stearyl (meth) acrylate, isostearyl (meth) acrylate, (meth) Glycidyl acrylate, 2-aminoethyl (meth) acrylate, γ- (methacryloyloxy) propyltrimethoxysilane, ethylene oxide adduct of (meth) acrylic acid, trifluoromethylmethyl (meth) acrylate, (meth) acrylic 2-trifluoromethylethyl acid, 2-perfluoroethylethyl (meth) acrylate, 2-perfluoroethyl-2-perfluorobutylethyl (meth) acrylate, 2-perfluoroethyl (meth) acrylate, ( Perfluoromethyl methacrylate), (meth) acrylic acid Diperfluoromethylmethyl, 2-perfluoromethyl-2-perfluoroethylethyl (meth) acrylate, 2-perfluorohexylethyl (meth) acrylate, 2-perfluorodecylethyl (meth) acrylate, (meta And (meth) acrylic acid ester monomers such as 2-perfluorohexadecylethyl acrylate;

  Examples of acrylonitrile monomers include acrylonitrile and methacrylonitrile.

  Examples of the aromatic vinyl monomer include styrene, vinyl toluene, α-methyl styrene, chlorostyrene, styrene sulfonic acid and salts thereof.

  Examples of the fluorine-containing vinyl monomer include perfluoroethylene, perfluoropropylene, and vinylidene fluoride.

  Examples of the silicon-containing vinyl monomer include vinyltrimethoxysilane and vinyltriethoxysilane.

  Other monomers constituting the vinyl polymer include maleic anhydride, maleic acid, monoalkyl esters and dialkyl esters of maleic acid; fumaric acid, monoalkyl esters and dialkyl esters of fumaric acid; maleimide, methylmaleimide, ethylmaleimide , Maleimide monomers such as propylmaleimide, butylmaleimide, hexylmaleimide, octylmaleimide, dodecylmaleimide, stearylmaleimide, phenylmaleimide, cyclohexylmaleimide; amide group-containing vinyl monomers such as acrylamide and methacrylamide; vinyl acetate, vinyl propionate, Vinyl esters such as vinyl pivalate, vinyl benzoate and vinyl cinnamate; alkenes such as ethylene and propylene; butadiene, iso Conjugated dienes such as Ren, vinyl chloride, vinylidene chloride, allyl chloride, allyl alcohol and the like.

  In the case where the component (A) is an oligomer or a polymer, the molecular weight distribution (ratio of weight average molecular weight (Mw) and number average molecular weight (Mn) measured by gel permeation chromatography (GPC)) is not particularly limited. , Preferably less than 1.8, more preferably 1.7 or less, even more preferably 1.6 or less, particularly preferably 1.5 or less, particularly preferably 1.4 or less, most preferably 1.3 or less. .

  In the GPC measurement in the present invention, a polystyrene gel column is usually used with chloroform or tetrahydrofuran as a mobile phase, and the molecular weight value is obtained in terms of polystyrene.

  When the component (A) is an oligomer or a polymer, the lower limit of the number average molecular weight is preferably 500, more preferably 3,000, and the upper limit is preferably 100,000, more preferably 40,000. If the molecular weight is less than 500, the original characteristics of the vinyl polymer tend to be hardly expressed, and if it exceeds 100,000, handling tends to be difficult.

The compound (A) is a compound having at least one polymerizable carbon-carbon double bond, but preferably has at least one substituent represented by the general formula (1) from the viewpoint of reactivity.
^{-Z-C (= O) -C} (R 1) = CH 2 (1)
(In the formula, R ¹ is hydrogen or a hydrocarbon group having a substituted or unsubstituted linear or branched structure having 1 to 20 carbon atoms, and a part of the hydrocarbon bond is an ether bond, ester bond, amino It may be substituted with a bond, an amide bond, etc. Z is selected from a hetero atom, NR ² (R ² is a hydrogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms). Group.)
Furthermore, when the component (A) is an oligomer or a polymer, the substituent is preferably at the molecular end, and more preferably only at the end.

R ¹ in the general formula (1) is hydrogen or a hydrocarbon group having a substituted or unsubstituted linear or branched structure having 1 to 20 carbon atoms, and part of the hydrocarbon bond is an ether bond, ester It may be substituted with a bond, amino bond, amide bond or the like. The substituted hydrocarbon group here means a group in which a hydrogen atom on a hydrocarbon group or a carbon atom is substituted with a group having a hetero atom.

R ¹ is preferably hydrogen or a hydrocarbon group having a straight chain or branched structure having 1 to 20 carbon atoms, such as a hydrogen atom; an alkyl group such as a methyl group or an ethyl group; a cycloalkyl group such as a cyclohexyl group. An aryl group such as a phenyl group; an aralkyl group such as a benzyl group; In these, a hydrogen atom or a methyl group is preferable from the availability of a raw material, and also a hydrogen atom is more preferable from the high polymerization reactivity.

Z in the general formula (1) is not particularly limited, and examples thereof include an oxygen group; a sulfur atom; and an amino group such as —NH— and —NCH ₃ —. In these, an oxygen atom and -NH- group are preferable from the ease of introduction | transduction, and an oxygen atom is more preferable.

  The number of substituents represented by the general formula (1) is not particularly limited, but when the component (A) is an oligomer or a polymer, the average number is less than 1 per molecule from the viewpoint that the compounds (A) are cross-linked. Since there exists a tendency for sclerosis | hardenability to become low, one or more is preferable on average. However, in order to adjust the hardness and flexibility of the cured product with respect to the compound (A) having one or more substituents represented by the general formula (1) on average per molecule, the average is less than 1 per molecule An oligomer or a polymer having a substituent represented by the general formula (4) may be added. Further, the substituent represented by the general formula (4) may be present in any of the side chain and / or the terminal of the molecule, but the molecular weight between the crosslinking points is uniform and large (preferably 500 to 100,000). From the viewpoint of obtaining good rubber elasticity, it is preferable to exist at the end of the molecule, and more preferable to exist only at the end of the molecule.

(Production method of component (A))
The method for producing the component (A) is not particularly limited, but when it is a vinyl polymer, it is generally produced by anionic polymerization or radical polymerization. Of these, radical polymerization is preferred because of the versatility of the monomer and ease of control. Among radical polymerizations, it is preferably produced by living radical polymerization or radical polymerization using a chain transfer agent, and the former is particularly preferable.

  The radical polymerization method used for the production of the component (A) is a method in which an azo compound or peroxide is used as a polymerization initiator, and a monomer having a specific functional group and a vinyl monomer are simply copolymerized. Can be classified into “radical polymerization methods” and “controlled radical polymerization methods” in which specific functional groups can be introduced at controlled positions such as terminals.

  The “general radical polymerization method” is a simple method. However, in this method, a monomer having a specific functional group is introduced into the polymer only in a probabilistic manner, so an attempt is made to obtain a polymer having a high functionalization rate. In such a case, it is necessary to use this monomer in a considerably large amount, and conversely, in the case of using a small amount, there is a problem that the proportion of the polymer in which this specific functional group is not introduced becomes large. Moreover, since it is free radical polymerization, there is also a problem that only a polymer having a wide molecular weight distribution and a high viscosity can be obtained.

  The “controlled radical polymerization method” further includes a “chain transfer agent method” in which a vinyl polymer having a functional group at a terminal is obtained by polymerization using a chain transfer agent having a specific functional group, It can be classified as “living radical polymerization method” in which a polymer having a molecular weight almost as designed can be obtained by growing the terminal without causing a termination reaction or the like.

  In the “chain transfer agent method”, a polymer having a high functionalization rate can be obtained, but a chain transfer agent having a considerably large amount of a specific functional group with respect to the initiator is required. There is an economic problem. Further, like the above-mentioned “general radical polymerization method”, there is also a problem that only a polymer having a wide molecular weight distribution and high viscosity can be obtained because of free radical polymerization.

  Unlike these polymerization methods, the “living radical polymerization method” is a radical polymerization that is difficult to control because the polymerization rate is high and a termination reaction due to coupling between radicals is likely to occur. It is difficult to obtain a polymer having a narrow molecular weight distribution (Mw / Mn is about 1.1 to 1.5), and the molecular weight can be freely controlled by the charging ratio of the monomer and the initiator.

  Therefore, the “living radical polymerization method” can obtain a polymer having a narrow molecular weight distribution and a low viscosity, and a monomer having a specific functional group can be introduced at almost any position of the polymer. The production method of the vinyl polymer having the specific functional group is more preferable.

  In the narrow sense, living polymerization refers to polymerization in which the terminal always has activity and the molecular chain grows, but in general, the terminal is inactivated and the terminal is activated. Pseudo-living polymerization in which is grown while in equilibrium. The definition in the present invention is also the latter.

  The “living radical polymerization method” has been actively researched by various groups in recent years.

  Examples thereof include those using a cobalt porphyrin complex as shown in Journal of the American Chemical Society (J. Am. Chem. Soc.), 1994, 116, 7943, “Atom transfer radical polymerization” using radical scavengers such as nitroxide compounds as shown in Macromolecules, 1994, 27, 7228, organic halides as initiators and transition metal complexes as catalysts. (Atom Transfer Radical Polymerization: ATRP).

  Among the “living radical polymerization methods”, the “atom transfer radical polymerization method” for polymerizing vinyl monomers using an organic halide or a sulfonyl halide compound as an initiator and a transition metal complex as a catalyst is the above-mentioned “living radical polymerization method”. In addition to the characteristics of ”, it has a halogen, which is relatively advantageous for functional group conversion reaction, at the end, and has a high degree of freedom in designing initiators and catalysts. Therefore, production of vinyl polymers having specific functional groups The method is more preferable.

  Examples of the atom transfer radical polymerization method include, for example, Matyjazewski et al., Journal of the American Chemical Society (J. Am. Chem. Soc.) 1995, 117, 5614, Macromolecules. 1995, 28, 7901, Science 1996, 272, 866, WO96 / 30421 pamphlet, WO97 / 18247 pamphlet or Sawamoto et al., Macromolecules 1995, 28, And the method described on page 1721.

  In the present invention, there is no particular restriction as to which of these methods is used, but basically, a controlled radical polymerization method is used, and a living radical polymerization method is preferred from the standpoint of ease of control, and particularly an atom. The transfer radical polymerization method is preferred.

(Introduction of functional groups)
In order to obtain the component (A), a known method can be used as a method for introducing a polymerizable carbon-carbon double bond represented by the general formula (1) into the polymer. Examples thereof include the methods described in paragraphs [0080] to [0091] of JP-A No. 2004-203932. Other than these methods, there is a method in which a (meth) acrylic polymer having a hydroxyl terminal is reacted with an isocyanate group and a monomer having a polymerizable carbon-carbon double bond as represented by formula (1), for example, 2 Examples include a method using-(meth) acryloyloxyethyl isocyanate.

(Low molecular weight compound)
In the curable compositions (I) and (II) of the present invention, a polymerizable carbon-carbon is used as the component (A) for the purpose of improving coating properties (reducing viscosity) and improving mechanical properties of the seal layer. Various low molecular weight compounds having one or more double bonds can be added. As the low molecular weight compound shown here, a radical reactive vinyl monomer is preferable, and a (meth) acrylic monomer is preferable in terms of radical reactivity. The (meth) acrylic monomer is not particularly limited as long as it is a monomer having a (meth) acryloyl group, and may be monofunctional or polyfunctional. Examples include (meth) acrylic acid ester monomers, (meth) acrylonitrile, (meth) acrylic acid and the like.

  When the low molecular weight compound is added, the total amount of the low molecular weight compound is not particularly limited, but the component (A) in the curable composition (I) or the curable composition (II) containing the low molecular weight compound is not limited. It is preferably 10% to 40% by weight, more preferably 15% to 35% by weight based on the total weight. Even when the low molecular weight compound is contained in both the curable composition (I) and the curable composition (II), the respective compositions of the curable composition (I) and the curable composition (II). In the above, it is preferable that the amount falls within the above range. If the total amount of the low molecular weight compound is less than 10% by weight relative to the total weight of the component (A), the viscosity of the composition may be high and workability may be deteriorated. The original characteristics of coalescence may be deteriorated.

<(B) component>
The curable compositions (I) and (II) of the present invention contain a photopolymerization initiator (B). By including the photopolymerization initiator (B) in the curable composition (I), the curable composition (I) filled in the visual recognition part when bonded can be cured by light irradiation. On the other hand, by including the photopolymerization initiator (B) in the curable composition (II), the curable composition (II) filled in the dark part when it is bonded is irradiated with light before bonding. It becomes possible to perform temporary curing. Although it does not specifically limit as photoinitiator (B) contained in curable composition (I) and (II), For example, acetophenone, propiophenone, benzophenone, xanthol, fluorin, benzaldehyde, anthraquinone, triphenyl Amine, carbazole, 3-methylacetophenone, 4-methylacetophenone, 3-pentylacetophenone, 2,2-diethoxyacetophenone, 4-methoxyacetophene, 3-bromoacetophenone, 4-allylacetophenone, p-diacetylbenzene, 3- Methoxybenzophenone, 4-methylbenzophenone, 4-chlorobenzophenone, 4,4′-dimethoxybenzophenone, 4-chloro-4′-benzylbenzophenone, 3-chloroxanthone, 3,9-dichloroxanthone, 3 Chloro-8-nonylxanthone, benzoyl, benzoin methyl ether, benzoin butyl ether, bis (4-dimethylaminophenyl) ketone, benzylmethoxy ketal, 2-chlorothioxanthone, 2,2-dimethoxy-1,2-diphenylethane 1-one, 1-hydroxy-cyclohexyl-phenyl-ketone, 2-hydroxy-2-methyl-1-phenyl-propan-1-one, 2-methyl-1- [4- (methylthio) phenyl] -2-morpho And linopropan-1-one, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1, and the like. Among these, phenyl ketone compounds are preferred in that they have tack-improving properties.

  In addition, an acylphosphine oxide photopolymerization initiator having excellent deep curability during UV irradiation can also be blended. Acylphosphine oxide polymerization initiators include 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide, bis (2,6-dimethoxybenzoyl)- 2,4,4-trimethyl-pentylphosphine oxide, bis (2,6-dimethylbenzoyl) -phenylphosphine oxide, bis (2,4,6-trimethylbenzoyl) -isobutylphosphine oxide, bis (2,6-dimethoxybenzoyl) ) -Isobutylphosphine oxide, bis (2,6-dimethoxybenzoyl) -phenylphosphine oxide, etc., preferably 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, bis (2,4,4) - trimethyl benzoyl) - phenyl phosphine oxide, bis (2,6-dimethoxybenzoyl) -2,4,4-trimethyl - a pentyl phosphine oxide. The above photo radical initiators may be used alone or in combination of two or more.

  In the curable composition of the present invention, the acylphosphine oxide and the phenyl ketone compound can be used in combination.

  The addition amount of the photo radical initiator (B) is 0.025 parts by weight to 3 parts by weight with respect to 100 parts by weight of the component (A) in the curable composition (I) and the curable composition (II). It is preferably 0.05 parts by weight to 2 parts by weight. When the amount is less than 0.025 parts by weight, the curable composition (I) and the curable composition (II) cannot obtain sufficient curability. If it exceeds 3 parts by weight, the physical properties of the cured product may be affected.

<(C) component>
The organic peroxide (C) contained in the curable composition (I) of the present invention is added as a radical polymerization initiator in a redox reaction by two-component contact.

  Examples of the organic peroxide (C) include hydroperoxide, dialkyl peroxide, peroxycarbonate, peroxycarboxylic acid, and esters thereof, diacyl peroxide, and the like. Among these, hydroperoxide is preferable from the viewpoint of storage stability and safety of the curable composition. Examples of the hydroperoxide include cumene hydroperoxide and t-butyl hydroperoxide. These peroxides may contain solvents such as toluene, xylene and water.

  The amount of the organic peroxide (C) added is preferably 0.1 to 2 parts by weight with respect to 100 parts by weight of the component (A) in the curable composition (I), and 0.2 parts by weight. It is more preferable that it is 1.5 parts by weight. If it is less than 0.1 parts by weight, the time required for curing at the time of two-component contact is long, and even if it is more than 2 parts by weight, no increase in the curing rate is observed with respect to the number of added parts, and the storage stability of the curable composition deteriorates. .

<(D) component>
The 4th period transition metal element compound (D) contained in curable composition (II) of this invention is added as a hardening accelerator of the redox reaction by 2 liquid contact.

  The fourth period transition metal element compound (D) is at least one selected from organic acid salts or metal chelate compounds of vanadium, titanium, chromium, manganese, iron, cobalt, nickel, copper, and a curable composition ( II) is preferable from the viewpoint of compatibility of the component (D) in the above. Among them, the transition metal species is more preferably any of vanadium, cobalt and copper from the viewpoint of reactivity, and vanadium is preferable from the viewpoint of reactivity. And more preferable.

  Examples of organic acid salts of vanadium include vanadium (III) acetate, vanadium (III) octanate, vanadium (III) naphthenate, vanadium (III) stearate, vanadyl (IV) acetate, vanadyl (IV) octanate, vanadyl (IV) naphthenate , Vanadyl (IV) stearate and the like. Examples of the metal chelate compound of vanadium include vanadium (III) acetylacetonate, vanadium (III) benzoylacetonate, vanadyl (IV) acetylacetonate, vanadyl (IV) benzoylacetonate, vanadyl (IV) porphyrin and the like. Among these, vanadium (III) acetylacetonate and vanadyl (IV) acetylacetonate are preferable in terms of availability and handling, and vanadium (III) acetylacetonate is more preferable in terms of compatibility.

  The amount of the fourth period transition metal compound (D) added is preferably 0.5 to 2 parts by weight with respect to 100 parts by weight of the component (A) in the curable composition (II). More preferably, it is 5 to 1.0 part by weight. If the amount is less than 0.5 parts by weight, the time required for curing at the time of two-component contact is long, and if it is more than 2 parts by weight, no increase in the curing rate is observed with respect to the number of added parts, compatibility with the curable composition, and curing. The storage stability of the composition is deteriorated.

<(E) component>
The reducing agent (E) contained in the curable composition (II) of the present invention is added as a curing accelerator for the redox reaction by two-component contact.

  The reducing agent (E) is preferably selected from at least one selected from tertiary amines, orthobenzoixsulfimides, mercaptans, thiourea compounds, and salts thereof.

  Tertiary amines include tertiary alkyl amines such as triethylamine, diisopropylethylamine, tri (n-propyl) amine, tri (n-butyl) amine, triamylamine, N, N-dimethylaniline, N, N- And tertiary aromatic amines such as dimethyl-p-toluidine.

  As mercaptans, 1-dodecanethiol, tetraethylene glycol (bis) (3-mercaptopropionate), trimethylolpropane (tris) (2-mercaptopropionate), tris- (3-mercaptopropionyloxy) -ethyl ) -Isocyanurate, pentaerythritol (tetrakis) (2-mercaptopropionate), bis (pentaerythritol) (hexakis) (2-mercaptopropionate), and the like.

  Examples of the thiourea compound include acetylthiourea, benzoylthiourea, ethylenethiourea, N, N′-dibutylthiourea, N, N′-dioctylthiourea and the like.

  Among these, a thiourea compound is preferable in terms of high reactivity and low odor, and N, N′-dibutylthiourea is more preferable in terms of availability and compatibility.

  Although the addition amount of a reducing agent (E) is based also on the kind of reducing agent to add, 0.1-15 weight part is preferable. In the case of a tertiary amine or mercaptan, the amount is preferably 0.5 to 15 parts by weight with respect to 100 parts by weight of the component (A) in the curable composition (II), and preferably 1 to 10 parts by weight. It is more preferable that When the amount is less than 0.5 part by weight, the time required for curing at the time of two-component contact is long. When the amount is more than 15 parts by weight, it is not preferable in terms of odor, and the storage stability of the curable composition is deteriorated. In the case of an orthobenzoixsulfimide or thiourea compound, the amount is preferably 0.1 to 1.5 parts by weight with respect to 100 parts by weight of the component (A) in the curable composition (II). More preferably, it is 2 to 1 part by weight. If it is less than 0.1 parts by weight, it takes a long time to cure at the time of two-component contact, and if it is more than 1.5 parts by weight, no improvement in the curing rate according to the number of added parts is observed, and storage of the curable composition is possible. Stability deteriorates.

<Other additives>
The curable compositions (I) and (II) of the present invention include a radical scavenger, a plasticizer, a silane coupling agent, a filler, a modifier, and other resin components as long as the effects of the present invention are not impaired. Other components such as can be contained. The radical scavenger mentioned here generally includes what are called antioxidants and light stabilizers. The antioxidant is not particularly limited, and examples thereof include ascorbic acid-based, hindered phenol-based, monophenol-based, bisphenol-based, and polyphenol-based antioxidants. Among these, hindered phenol-based antioxidants Is preferred. Similarly, Tinuvin 622LD, Tinuvin 144, CHIMASSORB 944LD, CHIMASSORB 119FL (all of which are manufactured by BASF Corporation); MARK LA-57, MARK LA-62, MARK LA-67, MARK LA-63, MARK LA-68 (above, All are manufactured by ADEKA Corporation); Sanol LS-770, Sanol LS-765, Sanol LS-292, Sanol LS-2626, Sanol LS-1114, Sanol LS-744 (all are manufactured by Sankyo Co., Ltd.) The indicated hindered amine light stabilizers can also be used. Specific examples of the antioxidant are also described in JP-A-4-283259 and JP-A-9-194731. The amount of the antioxidant used is preferably 0.05 to 5 parts by weight, more preferably 0.1 to 2 parts by weight, relative to 100 parts by weight of component (A). It is. If the amount used is smaller than this, a sufficient effect may not be obtained. If the amount used is larger than this, it is not only economically disadvantageous, but also the curable composition (I). When added to, the reactivity in two-liquid contact deteriorates with time.

  Examples of the light stabilizer include benzotriazole, hindered amine, and benzoate compounds. Among these, hindered amine compounds are preferable. The light stabilizer is preferably used in an amount of 0.1 to 10 parts by weight, more preferably 0.2 to 5 parts by weight per 100 parts by weight of component (A). If the amount used is smaller than this, sufficient effects may not be obtained. If the amount used is larger than this, it may not only be economically disadvantageous, but also a photo radical initiator. There is a possibility that the antioxidant is supplemented by the generated radicals, and the cured product is poorly cured, and the cured product does not exhibit good physical properties. Specific examples of the light stabilizer are also shown in JP-A-9-194731.

  Plasticizers include phthalates such as dibutyl phthalate, diheptyl phthalate, di (2-ethylhexyl) phthalate, butyl benzyl phthalate; dioctyl adipate, dioctyl sebacate, diisononyl- (cyclohexane-1,2-dicarboxylate) Non-aromatic dibasic acid esters such as: esters of polyalkylene glycols such as diethylene glycol dibenzoate and triethylene glycol dibenzoate; phosphate esters such as tricresyl phosphate and tributyl phosphate; chlorinated paraffins; Hydrocarbon oils such as partially hydrogenated terphenyl can be used alone or in admixture of two or more, but this is not always necessary. In addition, these plasticizers can also be mix | blended at the time of saturated hydrocarbon type polymer manufacture. The amount of the plasticizer used is preferably in the range of 5 to 200 parts by weight, more preferably 10 to 100 parts by weight, relative to 100 parts by weight of component (A). When the amount used is less than this, a sufficient effect may not be obtained, and when the amount used is larger than this, the mechanical properties of the obtained cured product may be lowered. The addition of a plasticizer is effective for adjusting physical properties and properties.

  Examples of the silane coupling agent include silane compounds having a reactive group such as an epoxy group, a carboxyl group, a methacryloyl group, and an isocyanate group. Specifically, trimethoxysilylbenzoic acid, γ-methacryloxypropyltrimethoxysilane, vinyltriacetoxysilane, vinyltrimethoxysilane, γ-isocyanatopropyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane, β -(3,4-epoxycyclohexyl) ethyltrimethylsilane and the like. These may be used alone or in combination of two or more. Although the content rate of the silane coupling agent component in the resin composition of this invention does not have limitation in particular, It is 0.1-20 weight part normally with respect to 100 weight part of (A) component, Preferably it is 0.3. -10 parts by weight. Addition of a silane coupling agent is effective for improving adhesiveness and water resistance.

  Examples of the filler include fine particle silica, glass beads, talc, styrene polymer particles, methacrylate polymer particles, ethylene polymer particles, and propylene polymer particles. Among them, inorganic fillers are preferable, and fine particle silica is particularly preferable. preferable. These may be used alone or in combination of two or more. Although the content rate of a filler component does not have limitation in particular, It is 20-150 weight part normally with respect to 100 weight part of (A) component, Preferably it is 50-100 weight part. By adding an inorganic filler, it is possible to improve the strength, moisture permeability resistance and adhesion.

  Examples of the modifier include polymerization initiation assistants, leveling agents, wettability improvers, surfactants, and the like. These may be used alone or in combination of two or more.

<Curable composition>
The curable compositions (I) and (II) of the present invention are prepared by mixing each component uniformly. The mixing method is not particularly limited, but for the curable composition (I), the components other than the organic peroxide (C) are thoroughly mixed, and then the organic peroxide (C) is mixed. It is preferable in terms of the stability of the composition and the safety of operation. In the case of mixing, the apparatus is not particularly limited, but it is prepared by appropriately mixing using a hand stirring, a mechanical stirring apparatus, a roll mill or the like.

  The curable composition (I) of the present invention is preferably cured by active energy rays, and more preferably by light (UV).

  In the case of curing with active energy rays, the active energy rays include light (UV) or electron beam, and the active energy ray source is not particularly limited, but depends on the properties of the photopolymerization initiator used. Examples thereof include a high pressure mercury lamp, a low pressure mercury lamp, an electron beam irradiation device, a halogen lamp, a light emitting diode, a semiconductor laser, and a metal halide.

  The curing temperature is preferably 0 ° C to 150 ° C, more preferably 5 ° C to 120 ° C.

<Coating amount of curable compositions (I) and (II)>
The ratio of the coating amount when the curable compositions (I) and (II) are respectively applied to a bonded base material (translucent protective cover board, image display module, etc.) is cured in the dark part of interest. The weight ratio of the curable composition (I) to (II), that is, (I) / (II) is preferably 0.1 to 100, more preferably 0.5 to 50. It is preferable to apply I) and (II) to the bonded substrate.

Method for Producing Image Display Device In the method for producing an image display device of the present invention, the image display module and the protective cover are bonded together by applying and curing the above curable composition by the method described below. Specifically, for example, as shown in FIGS. 1 to 6, application of a two-component curable composition on a bonded base material (translucent protective cover board, image display module, etc.), curable composition ( II) includes provisional curing by light irradiation, superposition of bonded substrates, curing by light and redox polymerization reaction.

  The bonding base material is a translucent protective cover board and an image display module, but the translucent protective cover board is not particularly limited, but is disposed on the screen display module, for example, a polyester resin, an acrylic type This is a cover made of resin such as resin, polycarbonate resin, or glass, and has a function of protecting the screen display module surface from scratches and damage from falling, and also has a design function. The shape and structure of the translucent protective cover board are not particularly limited. For example, the translucent protective cover board may have a multilayer structure composed of several kinds of resins, or a single layer structure formed of a single material. In addition, if necessary, the protective cover surface may be coated with a film or a film to prevent fingerprint adhesion, light reflection prevention, reflection and glare prevention, and the protective cover is provided with a touch panel function. Or a protective cover and a touch panel may be bonded together.

  The image display module to be bonded is not particularly limited, and is a liquid crystal module (LCD module), a touch sensor using the same, a plasma display panel, an E-ink type display module for electronic paper, and a SIPIX type display module. And display modules such as organic EL.

<Application of curable composition on bonded substrate>
As a coating method of the curable compositions (I) and (II) when the curable composition of the present invention is used as a filler for bonding an image display module, the curable composition (II) is used as a bonding group. The light-transmitting protective cover board and / or image display module, which is a material, is applied to a dark portion where light does not reach when the light-transmitting protective cover board and the image display module are bonded together, and a curable composition ( I) is applied to a portion of the light-transmitting protective cover board and / or image display module that does not come into contact with the curable composition (II).

  The order of applying each of the curable compositions (I) and (II) is not particularly limited, and after applying the curable composition (I) or (II), the other may be applied, or both components may be applied. May be applied simultaneously.

  The base material to which the curable compositions (I) and (II) are applied is not particularly limited, and if necessary, applied to one of the two target base materials (the translucent protective cover board and the image display module). Only the curable compositions (I) and (II) may be applied, or the curable compositions (I) and (II) may be separately applied to both of the two substrates. Moreover, you may apply | coat only curable composition (I) to either one base material, and may apply only (II) to the other base material.

  The application method to a bonding base material is not particularly limited, and various commonly used application methods can be used. For example, there are a method using a dispenser, a method using a coater, a method using a spray, and the like. A robot-controlled dispenser is preferred in terms of anti-sagging after application of the liquid composition and application accuracy for supplying a specific amount of the liquid composition to a specific site such as a dark part.

(Coating method of curable composition (II))
The curable composition (II) is applied to a dark part where light does not reach when the light-transmitting protective cover board and / or the image display module are bonded to each other. Apply to the part.

  The dark part where light does not reach when the translucent protective cover board and the image display module are bonded together is, for example, a black frame (black matrix) applied to the peripheral edge of the translucent protective cover board for the purpose of decoration, or an electrode of the touch panel This is a portion that is shaded when light is applied from the outside when the transparent protective cover board and the image display module are bonded together by a flexible printed circuit board (FPC) or the like connected to the image display module.

  Specifically, when the translucent protective cover board and the image display module are overlapped, the portion between the black matrix on the translucent protective cover board and the image display module becomes a dark part where light does not reach. .

  Examples of the method for applying the curable composition (II) to the dark portion by the black matrix include the method shown in FIG. 1, and the curable composition is applied to the black matrix 3 portion of the translucent protective cover board. (II) is applied (5 in FIG. 1). As another method, it may be applied to a dark part by the black matrix of the image display module, or may be applied to a dark part of both the translucent protective cover board and the image display module. Moreover, the coating thickness of the curable composition (II) applied to the dark part is not particularly limited. As shown in FIG. 2, the curable composition (II) is applied when two substrates are bonded together. You may contact the base material of the side which is not.

(Coating method of curable composition (I))
The curable composition (I) is applied to a portion of the translucent protective cover board and / or image display module that does not come into contact with the curable composition (II). As a method for applying the curable composition (I), for example, the method shown in FIG. As another method, the curable composition (I) can be applied to the image display module. In this case, the application range does not need to be limited, and the transparent protective cover board is overlaid. You may apply | coat to any part including the part which overlaps with the part of a black matrix. Furthermore, you may apply | coat to both the part which does not apply | coat curable composition (II) on a translucent protective cover board, and an image display module.

<Temporary curing method by photopolymerization reaction of curable composition (II)>
After applying the photopolymerization initiator (B) to the curable composition (II) and applying it to the bonded base material, it is irradiated with light or an electron beam from an active energy ray source as shown in FIG. And temporarily cured. Temporary curing as used herein refers to (A) in the curable composition (II), although the curable composition (II) is thickened and stopped flowing by suppressing the energy irradiation amount of the active energy ray. ) The state in which a part of the polymerizable carbon-carbon double bond in the component remains unreacted.

  The active energy ray source is not particularly limited, and examples thereof include a high-pressure mercury lamp, a low-pressure mercury lamp, an electron beam irradiation device, a halogen lamp, a light-emitting diode, a semiconductor laser, and a metal halide lamp depending on the properties of the photopolymerization initiator used. . The curing temperature is preferably 0 ° C to 150 ° C, more preferably 5 ° C to 120 ° C.

  Moreover, there is no limitation in particular as a method of irradiating an active energy ray, You may apply | coat only the curable composition (II) first like (FIG. 2), and may irradiate the whole bonding base material, (FIG. After applying both the curable composition (II) and the curable composition (I) as in 3), only the curable composition (II) may be selectively irradiated using a spot irradiation device or the like. I do not care.

  The irradiation amount of the active energy ray is not particularly limited, but depends on the photocurability of the curable composition (II), and the polymerizable carbon-carbon double in the component (A) in the curable composition (II). It is preferable that 40% to 70% of bonds remain with respect to the total amount before irradiation. In addition, the content rate of a carbon-carbon double bond can be calculated | required by methods, such as attenuation | damping total reflection (ATR) infrared spectroscopy of the surface of curable composition (II). If the energy irradiation amount of the active energy ray is too small, it is not sufficient to stop the flow of the curable composition (II) applied on the black matrix, and if it is too large, the curable composition (II) is cured. The curability of the curable composition (I) during the contact reaction is deteriorated.

<Lamination of bonded substrates>
After an appropriate amount of the curable compositions (I) and (II) is applied to a predetermined portion of the base material to be bonded, and the curable composition (II) is temporarily cured by irradiation with active energy rays, FIG. As shown, the overlapping is performed so that the liquid composition is on the inside. In superposition, the thickness of the liquid composition layer is controlled (Z-axis control) and the superposition position is controlled (alignment). At that time, it is necessary to be careful not to entrap bubbles or the like in the composition. There is. The method for superimposing is not particularly limited, and a known method can be arbitrarily used. In the superposition, the time required for the curable composition (I) to diffuse to a predetermined site and the Z-axis control and alignment state of the substrates to be bonded are maintained by light and redox polymerization reaction. Move on to curing. There is no particular limitation on the holding time, and the curable composition (I) is not necessarily in complete contact with the curable composition (II) in the dark part, but the curable composition (I) diffuses into the dark part. Further, it is more preferable that a part of the curable composition (I) is in contact with the temporarily cured curable composition (II) present in the dark part. In addition, although details of a curing method by photopolymerization reaction of the curable composition (I) will be described later, a part or the whole surface is irradiated with light so that the base material to be bonded is not shifted at the stage of holding the overlapping. By doing so, the curable composition (I) may be temporarily cured to temporarily fix the substrate.

<Curing method by redox polymerization reaction>
When the two-component curable composition is present in a dark part where light is not transmitted, the redox polymerization reaction proceeds by contacting the curable composition (I) and the curable composition (II) as described above. And can be cured (see FIG. 5). The redox polymerization reaction can be cured at room temperature, but in order to proceed the curing more rapidly, a treatment such as heating may be performed. 5-100 degreeC is preferable and the temperature in the case of a heating has more preferable 10-80 degreeC.

<Curing method by photopolymerization reaction>
The method for curing the curable composition (I) by a photopolymerization reaction is not particularly limited, and a photopolymerization initiator (B) is used for the curable composition (I), and light or electron beam is generated by an active energy ray source. Can be cured by irradiation (see FIG. 6). The active energy ray source is not particularly limited, and examples thereof include a high-pressure mercury lamp, a low-pressure mercury lamp, an electron beam irradiation device, a halogen lamp, a light-emitting diode, a semiconductor laser, and a metal halide lamp depending on the properties of the photopolymerization initiator used. . The curing temperature is preferably 0 ° C to 150 ° C, more preferably 5 ° C to 120 ° C.

  Also, after bonding between the cover board / display module and between the cover board with touch sensor / display module, until the liquid resin is sufficiently leveled, it is applied and bonded for the purpose of preventing displacement of each substrate. It is preferable to temporarily fix a part of. As a temporary fixing method, UV irradiation is preferable in that only a part can be fixed.

<Application>
As electric / electronic products equipped with a display device bonded with a curable composition of the present invention, portable electronic terminals such as televisions, mobile phones, smartphones, portable media players, tablets, digital cameras, personal computers, Electronic paper, car navigation systems, in-vehicle display meters, refrigerators equipped with display devices, microwave ovens, household appliances such as washing machines, game machines, slot machines, and the like. The present invention includes an electric / electronic device equipped with a flat panel display obtained by applying and curing the curable composition for laminating an image display module.

  Hereinafter, the present invention will be described in more detail based on examples, but the present invention is not limited thereby.

  In the following examples, “number average molecular weight” and “molecular weight distribution (ratio of weight average molecular weight to number average molecular weight)” were calculated by a standard polystyrene conversion method using gel permeation chromatography (GPC). However, LC Module 1 manufactured by Waters was used as the GPC system, polystyrene crosslinked gel was used as the GPC column (Shodex GPC K-804; manufactured by Showa Denko KK), and chloroform was used as the GPC solvent.

The “number of acryloyl groups introduced per polymer molecule” was calculated from the number average molecular weight determined by ¹ H-NMR analysis and GPC. (However, ¹ H-NMR was measured at 23 ° C. using Bruker ASX-400 and deuterated chloroform as a solvent.)

(Production Example 1-1, 1-2)
(1) Polymerization process n-butyl acrylate was deoxygenated. The inside of the stainless steel reaction vessel equipped with a stirrer was deoxygenated, cuprous bromide and a part of all n-butyl acrylate (described as initial charge monomer in Table 1) were charged and stirred with heating. Acetonitrile (described as “Acetonitrile for polymerization” in Table 1), diethyl 2,5-dibromoadipate (DBAE) or ethyl 2-bromobutanoate (BBE) as an initiator are added and mixed, and the temperature of the mixture is adjusted to about 80 ° C. At that stage, pentamethyldiethylenetriamine (hereinafter abbreviated as triamine) was added to initiate the polymerization reaction. The remaining n-butyl acrylate (described as an additional monomer in Table 1) was sequentially added to proceed the polymerization reaction. During the polymerization, triamine was appropriately added to adjust the polymerization rate. The total amount of triamine used during the polymerization is shown in Table 1 as a triamine for polymerization. As the polymerization proceeds, the internal temperature rises due to the heat of polymerization, so the polymerization was allowed to proceed while adjusting the internal temperature to about 80 ° C to about 90 ° C.
(2) Oxygen treatment step When the monomer conversion rate (polymerization reaction rate) was about 95% or more, an oxygen-nitrogen mixed gas was introduced into the gas phase part of the reaction vessel. While maintaining the internal temperature at about 80 ° C. to about 90 ° C., the reaction solution was heated and stirred for several hours to bring the polymerization catalyst in the reaction solution into contact with oxygen. Acetonitrile and unreacted monomer were removed by devolatilization under reduced pressure to obtain a concentrate containing a polymer. The concentrate was markedly colored.
(3) First crude purification Butyl acetate was used as a diluent solvent for the polymer. The concentrate of (2) was diluted with about 100 to 150 kg of butyl acetate with respect to 100 kg of the polymer, and a filter aid (Radiolite R900, Showa Chemical Industries) was added. After introducing an oxygen-nitrogen mixed gas into the gas phase part of the reaction vessel, the mixture was heated and stirred at about 80 ° C. for several hours. Insoluble catalyst components were removed by filtration. The filtrate was colored and slightly turbid due to the polymerization catalyst residue.
(4) Second crude purification The filtrate was charged into a stainless steel reaction vessel equipped with a stirrer, and adsorbents (Kyoward 700SEN, Kyoward 500SH) were added. After introducing an oxygen-nitrogen mixed gas into the gas phase and heating and stirring at about 100 ° C. for several hours, insoluble components such as an adsorbent were removed by filtration. The filtrate was almost clear and clear. The filtrate was concentrated to obtain an almost colorless and transparent polymer.
(5) (Meth) acryloyl group introduction step 100 kg of polymer is dissolved in about 100 kg of N, N-dimethylacetamide (DMAc), potassium acrylate (about 2 molar equivalents relative to terminal Br group), heat stabilizer (H -TEMPO: 4-hydroxy-2,2,6,6-tetramethylpiperidine-n-oxyl) and an adsorbent (Kyoward 700SEN) were added, and the mixture was heated and stirred at about 70 ° C for several hours. DMAC was distilled off under reduced pressure, the polymer concentrate was diluted with about 100 kg of toluene with respect to 100 kg of the polymer, a filter aid was added, the solid content was filtered off, the filtrate was concentrated, and an acryloyl group was added to the end. Polymers [P1] and [P2] having Table 1 shows the number of acryloyl groups introduced per molecule of the obtained polymer, the number average molecular weight, and the molecular weight distribution.

(Production Example 2-1)
Polymer (P1) 20 parts by weight, [P2] 80 parts by weight, and 2-hydroxyethyl acrylate (Kyoeisha Chemical Co., Ltd. Light Ester HOA) having, as component (A), an acryloyl group at the terminal as described in Production Example 1 ) 10 parts by weight, 20 parts by weight of N, N′-dimethylacrylamide (manufactured by Kojin Co., Ltd.) is added to the minicup, and 2-hydroxy-2-methyl-1-phenyl-propane-1 is used as component (B). -ON (BASF DAROCURE 1173) 0.8 parts by weight, (2,4,6-trimethylbenzoyl) -diphenylphosphine oxide (BASF LUCIRIN TPO) 0.1 parts by weight, and after stirring and mixing, (C ) Add 0.65 parts by weight of cumene hydroperoxide 80% cumene solution (Park Mill H-80 manufactured by NOF Corporation) as a component and stir The curable composition (I-1) was obtained by mixing.

(Production Examples 2-2 and 2-3)
Each curable composition (I-2, I-3) was obtained by the method similar to manufacture example I-1 by the mixture ratio of the following Table 2.

(Production Example 3-1)
As the component (A) described in Production Example 1, 40 parts by weight of the polymer having an acryloyl group at the end [P1] and 60 parts by weight of [P2], and as the component (A), N, N′-dimethylacrylamide ( 30 parts by weight (manufactured by Kojin Co., Ltd.), (2,4,6-trimethylbenzoyl) -diphenylphosphine oxide (LUCIRIN TPO, manufactured by BASF) 1 part by weight as component (B), and vanadium (III) as component (D) Add 32.5 parts of a uniform mixture of 1 part by weight of acetylacetonate (manufactured by Aldrich) and 0.5 part of N, N′-dibutylthiourea (manufactured by Tokyo Chemical Industry Co., Ltd.) as component (E) to each minicup. The curable composition (II-1) was obtained by stirring and mixing.

(Production Examples 3-2 to 3-4)
In the same manner as in Production Example 3-1, curable compositions (II-2 to II-4) were obtained at the blending ratios shown in Table 3 below.

Abbreviations of each component in Table 2 and Table 3 are as follows.
HEA: 2-hydroxyethyl acrylate (Kyoeisha Chemical Co., Ltd. light ester HOA)
THF-A: 2-tetrahydrofurfuryl acrylate (Kyoeisha Chemical Co., Ltd. light acrylate THF-A)
DMAA: N, N′-dimethylacrylamide (manufactured by Kojin Co., Ltd.)
ISTA: Isostearyl acrylate (manufactured by Osaka Organic Chemical Industry Co., Ltd.)
1173: 2-hydroxy-2-methyl-1-phenyl-propan-1-one (DAROCURE 1173 manufactured by BASF)
TPO: (2,4,6-trimethylbenzoyl) -diphenylphosphine oxide (LUSFIRIN TPO manufactured by BASF)
CHP: Cumene hydroperoxide (Park Mill H-80 manufactured by NOF Corporation)
V (acac) 3: Vanadium (III) acetylacetonate (manufactured by Aldrich)
DBTU: N, N′-dibutylthiourea (manufactured by Tokyo Chemical Industry Co., Ltd.)
TAA: Triamylamine (branched mixture) (manufactured by Tokyo Chemical Industry Co., Ltd.)

(Examples 1-5, Comparative Examples 1-3)
The curable composition (II) shown in Table 4 was formed on a black matrix portion of a 0.7 mm thick glass cover glass having a black matrix having a width of 0.5 cm and a thickness of 0.05 mm. After dispensing a predetermined amount as shown in FIG. 2 so as to be 2 mm, the UV irradiation device manufactured by Fusion UV System (model: LIGHT HAMMER 6, light source: mercury lamp lamp, peak illuminance 600 mW / cm ² ) is listed in Table 4. Irradiation was performed with the integrated light amount, and temporary curing was performed. Subsequently, a predetermined amount of the curable composition (I) was dispensed as shown in FIG. 1 so as to have a film thickness of 0.2 mm in a portion having no black matrix, and then bonded to the LCD module (FIG. 4). Irradiation was performed with a UV irradiation apparatus (model: LIGHT HAMMER 6, light source: mercury lamp lamp, peak illuminance 600 mW / cm ² ) (integrated light amount: 6000 mJ / cm ² ) manufactured by Fusion UV System, and an image display device was obtained.

  After the 500 cycles test of heat shock (85 ° C. to 40 ° C.) of the obtained image display device, the LCD module was energized at room temperature to erode the colored visual recognition part derived from the curable composition (II). The presence or absence of contamination of the display part due to leakage of uncured material to the outer edge of the LCD module and intrusion of uncured material into the LCD module was confirmed.

  In Examples 1 to 5, leakage of the curable compositions (I) and (II) was not confirmed after the heat shock test, but the curable composition (II) containing no photopolymerization initiator (B) was used. In Comparative Examples 1 and 3, the curable composition (II) cannot be temporarily cured by light irradiation. Therefore, when the width of the black matrix is narrow as in this experiment, the curable composition (I) is bonded. Leakage to the outer edge cannot be suppressed, and erosion of the curable composition (II) into the visible region of the coloring, leakage of the uncured curable composition (I) or (II) to the outer edge of the LCD module, LCD module Contamination of the display part due to intrusion into the interior was confirmed. Further, as in Comparative Example 2, when the curable composition (II) containing the photopolymerization initiator (B) was completely cured by light irradiation, the cured product of the curable composition (II) was a black matrix. Since it was fixed underneath, no erosion was observed in the visible region of coloring derived from the curable composition (II), but the contact reactivity with the curable composition (I) was inferior. Leakage of the uncured composition (I) to the outer edge of the LCD module and contamination of the display part due to penetration into the LCD module were confirmed.

1. Translucent protective cover board (viewing part)
2. 2. Image display module or LCD module Black matrix 4. Curable composition I
5. Curable composition II
6). Curable composition II (after temporary curing by light irradiation)
7). Curable composition II (after curing by two-component contact)
8). Curable composition I (after curing by light irradiation)

Claims (14)

A curable composition (I) containing a compound (A) having one or more polymerizable carbon-carbon double bonds, a photopolymerization initiator (B), and an organic peroxide (C);
A translucent protective cover board using the curable composition (II) containing the compound (A), photopolymerization initiator (B), fourth-period transition metal element compound (D), and reducing agent (E) A method for manufacturing an image display device for bonding an image display module together,
The translucent protective cover board and / or the image display module is coated with the curable composition (II) in a dark portion where light is not transmitted when the translucent protective cover board and the image display module are bonded together. The curable composition (I) is applied to a portion of the protective protective cover board and / or image display module that does not come into contact with the curable composition (II), and the curable composition (II) is temporarily cured by light irradiation. After performing, the translucent protective cover board and the image display apparatus are bonded together, the curable composition (I) is brought into contact with the curable composition (II) that has been temporarily cured, and light irradiation is performed. . The method for producing an image display device according to claim 1, wherein the component (A) of the curable composition (I) and / or the curable composition (II) is a polymer or an oligomer. 3. The method for producing an image display device according to claim 2, wherein the polymer or oligomer of the component (A) is a vinyl polymer. (A) Component vinyl polymer is polyisobutylene, hydrogenated polyisoprene, hydrogenated polybutadiene, (meth) acrylic acid monomer, acrylonitrile monomer, aromatic vinyl monomer, fluorine-containing vinyl monomer and silicon-containing 4. The method for producing an image display device according to claim 3, wherein at least one polymer selected from polymers produced by mainly polymerizing monomers selected from the group consisting of vinyl monomers is selected. The polymerizable carbon-carbon double bond in the component (A) is represented by the general formula (1), and the method for producing an image display device according to any one of claims 1 to 4.
^{-Z-C (= O) -C} (R 1) = CH 2 (1)
(In the formula, R ¹ is hydrogen or a hydrocarbon group having a substituted or unsubstituted linear or branched structure having 1 to 20 carbon atoms, and a part of the hydrocarbon bond is an ether bond, ester bond, amino It may be substituted with a bond, an amide bond, etc. Z is selected from a hetero atom, NR ² (R ² is a hydrogen atom or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms). Group.)   The addition amount of the component (B) is 0.025 to 3 parts by weight with respect to 100 parts by weight of the component (A) in the curable compositions (I) and (II). Item 6. A method for manufacturing an image display device according to any one of Items 1 to 5.   The addition amount of the component (C) is 0.1 to 2 parts by weight with respect to 100 parts by weight of the component (A) in the curable composition (I). A method for manufacturing an image display device according to any one of the above.   (C) A component is hydroperoxide, The manufacturing method of the image display apparatus in any one of Claims 1-7 characterized by the above-mentioned.   The amount of component (D) added is 0.5 to 2 parts by weight per 100 parts by weight of component (A) in the curable composition (II). A method for manufacturing an image display device according to any one of the above.   The component (D) is at least one selected from vanadium, titanium, chromium, manganese, iron, cobalt, nickel, an organic acid salt of copper, or a metal chelate compound. The manufacturing method of the image display apparatus of description.   The amount of component (E) added is 0.1 to 15 parts by weight per 100 parts by weight of component (A) in curable composition (II). A method for manufacturing an image display device according to any one of the above.   The component (E) is at least one selected from tertiary amines, orthobenzoixsulfimide, mercaptans, thiourea compounds, and salts thereof, according to any one of claims 1 to 11, Manufacturing method of image display apparatus.   An image display device manufactured by the method according to claim 1. An electric / electronic device equipped with the image display device according to claim 13.