Stacked optical films and image display devices

Abstract

To provide a laminated optical film in which at least an iodine-based polarizer and an optical film are laminated via an adhesive layer, and in which the adhesive layer has two or more functions improved in a well-balanced manner. [Solution] A laminated optical film in which at least an iodine-based polarizer and an optical film are laminated via an adhesive layer, wherein the adhesive layer has a two-layer structure consisting of a first adhesive layer on the iodine-based polarizer side and a second adhesive layer on the optical film side, the first adhesive layer is formed of a first cured layer of a first adhesive composition, and the logPow representing the octanol / water partition coefficient based on the weighted average of the mole fractions of monomer components contained in the first adhesive composition is 2.5 or more, and the second adhesive layer is formed of a second cured layer of a second adhesive composition, and the logPow representing the octanol / water partition coefficient based on the weighted average of the mole fractions of monomer components contained in the second adhesive composition is less than 2.5.

Description

[Technical Field]

[0001] The present invention relates to a laminated optical film in which at least an iodine-based polarizer and an optical film are laminated via an adhesive layer. This laminated optical film can form image display devices such as mobile phones, car navigation systems, personal computer monitors, and televisions. [Background technology]

[0002] Image display devices such as mobile phones, car navigation systems, computer monitors, and televisions are equipped with laminated optical films in which multiple optical films are laminated with adhesive or tack layers in between. Transparent resin films such as phase difference films, polarizers, and transparent protective films are used as optical films.

[0003] In recent years, there has been a trend to modify the adhesive layer in laminated optical films, at least one of which includes a polarizer, in order to impart various functions. For example, Patent Document 1 below describes an optical laminate comprising a polarizer, a first cured product layer, a phase difference layer, and an adhesive layer in that order, wherein the polarizer is made of a polyvinyl alcohol resin containing iodine, the first cured product layer is a cured product of an active energy curable composition, the phase difference layer includes at least one phase difference expression layer which is a polymer of a polymerizable liquid crystal compound, the adhesive layer has an iodine content of 900 mg / kg or less after the optical laminate is stored at a temperature of 80°C and a relative humidity of 90% for 250 hours, and the polarizer and the first cured product layer are in direct contact, and the first cured product layer and the phase difference layer are in direct contact.

[0004] Patent Document 2 below describes an optical laminate having a polarizer containing a polyvinyl alcohol-based resin and a phase difference body containing a cured polymerizable liquid crystal compound, wherein the optical laminate has a first adhesive layer provided in contact with the polarizer and a second adhesive layer provided in contact with the phase difference body between the polarizer and the phase difference body, and preferably the first adhesive layer has a tensile modulus of 2000 MPa or more at a temperature of 25°C, and the second adhesive layer has a tensile modulus of 1900 MPa or less at a temperature of 25°C. [Prior art documents] [Patent Documents]

[0005] [Patent Document 1] Japanese Patent Publication No. 2021-113969 [Patent Document 2] Japanese Patent Publication No. 2022-110684 [Overview of the project] [Problems that the invention aims to solve]

[0006] As a result of diligent research by the present inventors, it was found that the technology described in Patent Document 1 above does not sufficiently suppress the corrosion of panels under high temperature and high humidity conditions, and there is room for further improvement. Furthermore, it was found that the technology described in Patent Document 2 above has room for further improvement in terms of enabling the adhesive layer to exhibit two or more functions.

[0007] The present invention was developed in view of the above circumstances, and aims to provide a laminated optical film in which at least an iodine-based polarizer and an optical film are laminated via an adhesive layer, and in which two or more functions of the adhesive layer are improved in a well-balanced manner. [Means for solving the problem]

[0008] The above problem can be solved by the following configuration. That is, the present invention is a laminated optical film in which at least an iodine-based polarizer and an optical film are laminated via an adhesive layer, wherein the adhesive layer has a two-layer structure of a first adhesive layer on the iodine-based polarizer side and a second adhesive layer on the optical film side. The first adhesive layer is formed of a first cured product layer of a first adhesive composition, and the logPow representing the octanol / water partition coefficient, obtained by the weighted average of the molar fractions of the monomer components contained in the first adhesive composition, is 2.5 or more. The second adhesive layer is formed of a second cured product layer of a second adhesive composition, and the logPow representing the octanol / water partition coefficient, obtained by the weighted average of the molar fractions of the monomer components contained in the second adhesive composition, is less than 2.5. The present invention relates to a laminated optical film (1).

[0009] In the above laminated optical film (1), the laminated optical film (2) in which the first cured product layer has a moisture permeability of 150 g / m 2 ·24 h or less is preferable.

[0010] In the above laminated optical film (1) or (2), the laminated optical film (3) in which the optical film is a liquid crystal-based retardation film is preferable.

[0011] In the above laminated optical film (3), the laminated optical film (4) in which the thickness of the retardation film is 5 μm or less is preferable.

[0012] In any of the above laminated optical films (1) to (4), the laminated optical film (5) in which the thickness of the first adhesive layer is 5 μm or less is preferable.

[0013] In any of the above laminated optical films (1) to (5), the laminated optical film (6) in which the thickness of the second adhesive layer is 3 μm or less is preferable.

[0014] In any of the above laminated optical films (1) to (6), the laminated optical film (7) in which the thickness of the iodine-based polarizer is 8 μm or less is preferable.

[0015] In any one of the above laminated optical films (1) to (7), the first adhesive composition contains at least a (meth)acrylate compound and a photopolymerization initiator, and as the (meth)acrylate compound, a laminated optical film (8) containing a (meth)acrylate (A) having a cyclic hydrocarbon skeleton in the molecule is preferred.

[0016] In the above laminated optical film (8), a laminated optical film (9) in which the first adhesive composition contains 70 parts by mass or more of the (meth)acrylate (A) when the total amount of the (meth)acrylate compound is 100 parts by mass is preferred.

[0017] In the above laminated optical film (8) or (9), a laminated optical film (10) in which the (meth)acrylate (A) is a compound having 5 to 12 carbon atoms constituting the cyclic hydrocarbon skeleton in the molecule is preferred.

[0018] In any one of the above laminated optical films (8) to (10), a laminated optical film (11) in which the (meth)acrylate (A) is at least a bifunctional or higher (meth)acrylate is preferred.

[0019] In any one of the above laminated optical films (8) to (11), the (meth)acrylate (A) has the following formulas (A1) to (A4);

Chemical formula

[0020] In any one of the above laminated optical films (8) to (12), a laminated optical film (13) in which the first adhesive composition further contains a (meth)acrylate (B) containing a hydroxyl group is preferred.

[0021] In any of the above laminated optical films (8) to (13), a laminated optical film (14) is preferred in which the content of (meth)acrylate (A) relative to (meth)acrylate (B) is in the range of 2 to 6 times.

[0022] In any of the above laminated optical films (8) to (14), the laminated optical film (15) is preferable in which the adhesive composition contains 5 to 25 parts by mass of (meth)acrylate (B) when the total amount of the (meth)acrylate compound is 100 parts by mass.

[0023] Furthermore, the present invention relates to an image display device (16) comprising any of the above-mentioned laminated optical films (1) to (15).

[0024] Furthermore, the present invention relates to an organic EL display device (16) comprising any of the above-mentioned laminated optical films (1) to (15). [Effects of the Invention]

[0025] The laminated optical film according to the present invention is a laminated optical film in which at least an iodine-based polarizer and an optical film are laminated with an adhesive layer in between, and the adhesive layer is formed in a two-layer structure consisting of a first adhesive layer on the iodine-based polarizer side and a second adhesive layer on the optical film side. The first adhesive layer is formed of a first cured layer of a first adhesive composition and is designed so that logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of the monomer components contained in the first adhesive composition, is 2.5 or more. On the other hand, the second adhesive layer is formed of a second cured layer of a second adhesive composition and is designed so that logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of the monomer components contained in the second adhesive composition, is less than 2.5. In other words, the iodine-based polarizer side of the adhesive layer designed in a two-layer structure has a logPow of 2.5 or more and exhibits hydrophobicity, while the optical film side of the adhesive layer has a logPow of less than 2.5 and exhibits hydrophilicity. Therefore, in the laminated optical film according to the present invention, the hydrophobicity and hydrophilicity of the adhesive layer differ on the iodine-based polarizer side and the optical film side, resulting in a balanced improvement of two or more functions with respect to the adhesive layer.

[0026] In the laminated optical film according to the present invention, the moisture permeability of the first cured layer constituting the iodine-based polarizer side of the adhesive layer designed in a two-layer structure is 150 g / m². 2 If the exposure time is 24 hours or less, the hydrophobicity of the adhesive layer on the iodine-based polarizer side increases further, resulting in a more balanced improvement in the two or more functions of the adhesive layer.

[0027] The following describes an example in which two or more functions of the adhesive layer are improved in a balanced manner in the laminated optical film according to the present invention. For example, if the laminated optical film according to the present invention is a laminated optical film in which at least an iodine-based polarizer and a liquid crystal phase difference film are laminated via an adhesive layer, the adhesive layer improves in a balanced manner in terms of its barrier function for the iodine-based polarizer and its adhesion function for the phase difference film. This point will be explained below.

[0028] First, let's explain the barrier function of the adhesive layer for iodine-based polarizers. When a laminated optical film, in which at least an iodine-based polarizer and a liquid crystal phase difference film are laminated via an adhesive layer, is incorporated into an image display device and exposed to high temperature and high humidity, iodine in the iodine-based polarizer penetrates the adhesive layer and phase difference film, either alone or via water, and eventually reaches beyond the phase difference film, for example, the panel or sensor of the image display device, where the iodine corrodes them. As a result, the panel or sensor of the image display device may deteriorate, or the image display function may be significantly impaired. However, if the first adhesive layer on the iodine-based polarizer side is formed by a first cured layer of a first adhesive composition designed with a logPow of 2.5 or higher, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of monomer components, then the adhesive layer exhibits a function that significantly inhibits iodine migration, i.e., a barrier function.

[0029] On the other hand, if the second adhesive layer on the phase difference film side is formed by a second cured layer of a second adhesive composition designed so that logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of monomer components, is less than 2.5, the adhesive layer will exhibit adhesion to the phase difference film.

[0030] As described above, for example, if the laminated optical film according to the present invention is a laminated optical film in which at least an iodine-based polarizer and a liquid crystal phase difference film are laminated via an adhesive layer, then with respect to the adhesive layer, two or more functions, specifically a barrier function for the iodine-based polarizer and an adhesion function for the phase difference film, are improved in a well-balanced manner. [Brief explanation of the drawing]

[0031] [Figure 1] This figure shows an example of an image display device equipped with a laminated optical film according to the present invention. [Modes for carrying out the invention]

[0032] Figure 1 shows an example of an image display device equipped with a laminated optical film according to the present invention. The image display device A shown in Figure 1 is an organic EL image display device equipped with an organic light-emitting diode panel 7, and includes a laminated optical film 10 in which an iodine-based polarizer 1 and a phase difference film 2 are laminated via an adhesive layer 3. The adhesive layer 3 is formed in a two-layer structure consisting of a first adhesive layer 31 on the iodine-based polarizer 1 side and a second adhesive layer 32 on the phase difference film 2 side. In the present invention, the laminated optical film may consist of three or more optical films, provided that it comprises at least an iodine-based polarizer 1 → adhesive layer 3 (a two-layer structure consisting of a first adhesive layer 31 on the iodine-based polarizer 1 side and a second adhesive layer 32 on the phase difference film 2 side) → phase difference film 2, starting from the outer surface (visual surface) towards the inner surface. In the embodiment shown in Figure 1, the image display device A comprises, in order from the outermost surface toward the organic light-emitting diode panel 7, a transparent protective film 6 → a third adhesive layer 5 → an iodine-based polarizer 1 → adhesive layer 3 (a two-layer structure consisting of a first adhesive layer 31 on the iodine-based polarizer 1 side and a second adhesive layer 32 on the phase difference film 2 side) → a phase difference film 2 → an adhesive layer 4 → an organic light-emitting diode panel 7. As described above, even when exposed to high temperature and high humidity, the laminated optical film 10 according to this embodiment prevents iodine contained in the iodine polarizer from penetrating the phase difference film 2 and the adhesive layer 4, and furthermore, the organic light-emitting diode panel 7 or touch sensor (not shown), by the barrier function of the adhesive layer 3, particularly the first adhesive layer 31 on the iodine polarizer 1 side, thus effectively preventing corrosion of the panel or sensor of the image display device. In addition, the laminated optical film 10 according to this embodiment exhibits excellent adhesion of the adhesive layer to the phase difference film due to the adhesion function of the adhesive layer 3, particularly the second adhesive layer 32 on the phase difference film 2 side.

[0033] The following describes various optical films that can constitute the laminated optical film according to the present invention. The optical film is not particularly limited and examples include iodine-based polarizers, phase difference films, liquid crystal-based phase difference films (phase difference layers), and transparent protective films.

[0034] <Iodine-based polarizers> In the present invention, the iodine-based polarizer is not particularly limited, and various types can be used. Examples of iodine-based polarizers include hydrophilic polymer films such as polyvinyl alcohol-based films, partially formalized polyvinyl alcohol-based films, and partially saponified ethylene-vinyl acetate copolymer films, to which iodine is adsorbed and then uniaxially stretched. The thickness of the polarizer can be, for example, 3 to 20 μm.

[0035] However, in this invention, from the viewpoint of improving heat resistance in harsh environments at high temperatures, it is preferable to use a thin polarizer with a thickness of 3 μm or more and 15 μm or less as the iodine-based polarizer. It is particularly preferable that the thickness be 12 μm or less, even more preferably 10 μm or less, and especially preferably 8 μm or less. Such thin polarizers have less thickness variation, excellent visibility, and excellent resistance to thermal shock due to minimal dimensional change.

[0036] Iodine-based polarizers, made by dyeing a polyvinyl alcohol-based film with iodine and uniaxially stretching it, can be produced, for example, by dyeing the polyvinyl alcohol by immersing it in an aqueous solution of iodine and stretching it to 3 to 7 times its original length. Boric acid, zinc sulfate, zinc chloride, etc., may be included as needed, or the film may be immersed in an aqueous solution of potassium iodide, etc. Furthermore, if necessary, the polyvinyl alcohol-based film may be immersed in water and washed before dyeing. Washing the polyvinyl alcohol-based film with water cleans away dirt and anti-blocking agents from the film surface, and also prevents uneven dyeing by swelling the film. Stretching may be performed after dyeing with iodine, while dyeing, or after stretching. Stretching can also be performed in aqueous solutions of boric acid or potassium iodide, or even in a water bath.

[0037] Typical examples of thin iodine-based polarizers include: Patent No. 4751486 specification, Patent No. 4751481 specification, Patent No. 4815544 specification, Patent No. 5048120 specification, International Publication No. 2014 / 077599 pamphlet, International Publication No. 2014 / 077636 pamphlet, Examples include thin polarizers described in the text or thin polarizers obtained from the manufacturing methods described therein.

[0038] As for the thin polarizers, among manufacturing methods that include a step of stretching in a laminated state and a step of dyeing, those obtained by a manufacturing method that includes a step of stretching in a boric acid aqueous solution, as described in Japanese Patent No. 4751486, Japanese Patent No. 4751481, and Japanese Patent No. 4815544, are preferred because they can be stretched to a high magnification and their polarization performance can be improved. In particular, those obtained by a manufacturing method that includes a step of auxiliary air stretching before stretching in a boric acid aqueous solution, as described in Japanese Patent No. 4751481 and Japanese Patent No. 4815544, are preferred. These thin polarizers can be obtained by a manufacturing method that includes a step of stretching a polyvinyl alcohol-based resin (hereinafter also referred to as PVA-based resin) layer and a stretching resin substrate in a laminated state and a step of dyeing. With this manufacturing method, even if the PVA-based resin layer is thin, it is possible to stretch it without problems such as breakage due to stretching because it is supported by the stretching resin substrate.

[0039] The adhesive layer side of the iodine-based polarizer may be subjected to surface modification treatment before the adhesive layer is formed. Examples of surface modification treatments include corona treatment, plasma treatment, and itro treatment, with corona treatment being particularly preferred. Corona treatment generates reactive functional groups such as carbonyl groups and amino groups on the polarizer surface, improving adhesion to the adhesive layer. In addition, the ashing effect removes foreign matter from the surface and reduces surface irregularities, making it possible to manufacture a laminated optical film with excellent appearance characteristics.

[0040] Furthermore, the adhesive layer side of the polarizer may be coated with an easy-adhesion composition before the adhesive layer is formed to create an easy-adhesion layer. Examples of easy-adhesion compositions include aqueous solutions containing a monofunctional radical polymerizable compound represented by general formula (1), which will be described later, and which can also be incorporated into the adhesive composition.

[0041] <Phase difference film> Examples of phase difference films include birefringent films made by uniaxial or biaxial stretching of polymer materials, liquid crystal polymer orientation films, and films in which a liquid crystal polymer orientation layer is supported by a film. The thickness of the film constituting the phase difference film is not particularly limited, but it is generally around 1 to 150 μm.

[0042] As for the phase difference film, the following formulas (1) to (3): 0.70 <Re

[0450] / Re

[0550] <0.97···(1) 1.5 × 10 -3 <Δn<6×10 -3 ...(2) 1.13 <NZ<1.50···(3) A reverse wavelength-dispersive phase difference film that satisfies the following equation may also be used: (In the formula, Re

[0450] and Re

[0550] are the in-plane phase difference values ​​of the phase difference film measured with light of wavelengths 450 nm and 550 nm at 23°C, respectively; Δn is the in-plane birefringence nx-ny when the refractive indices in the slow axis direction and the fast axis direction of the phase difference film are nx and ny, respectively; and NZ is the ratio of the thickness-direction birefringence nx-nz to the in-plane birefringence nx-ny when nz is the refractive index in the thickness direction of the phase difference film).

[0043] In the present invention, a liquid crystal phase difference film is preferred as the phase difference film. Liquid crystal phase difference films are generally thin, for example, 5 μm or less in thickness. However, as mentioned above, even if a laminated optical film comprising, for example, an iodine-based polarizer and a liquid crystal phase difference film is exposed to high temperature and high humidity, the iodine contained in the iodine-based polarizer remains within the adhesive layer due to the barrier function of the adhesive layer. Therefore, even a thin liquid crystal phase difference film can sufficiently prevent corrosion of the panel or sensor of the image display device. When forming the liquid crystal phase difference layer, a liquid crystalline compound is preferably used. A solvent containing the liquid crystalline compound can be applied to the substrate using, for example, a wire bar, gap coater, comma coater, gravure coater, or slot die. In this case, the applied liquid crystalline solution may be air-dried or heat-dried. It is preferable to apply the liquid crystalline solution at a concentration lower than the isotropic phase-liquid crystal phase transition concentration, i.e., in an isotropic phase state. In this case, it can be stably oriented by methods such as rubbing or photo-alignment.

[0044] <Adhesive layer> The adhesive layer of the laminated optical film according to the present invention is formed in a two-layer structure consisting of a first adhesive layer on the iodine-based polarizer side and a second adhesive layer on the optical film side. From the viewpoint of thinning the laminated optical film, the thickness of the first adhesive layer is preferably 5 μm or less, and more preferably 3 μm or less. Similarly, the thickness of the second adhesive layer is preferably 3 μm or less, and more preferably 2 μm or less.

[0045] The first adhesive layer is formed from the first cured layer of the first adhesive composition. The first adhesive composition is designed such that logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of the monomer components it contains, is 2.5 or greater.

[0046] The octanol / water partition coefficient (logPow) is an indicator of a substance's lipophilicity and represents the logarithm of its octanol / water partition coefficient. A high logPow indicates lipophilicity, which in turn means hydrophobicity. While logPow values ​​can be measured (using the flask immersion method described in JIS-Z-7260), they can also be calculated. In this specification, logPow values ​​calculated using CambridgeSoft ChemDraw Ultra are used.

[0047] In the laminated optical film according to the present invention, the moisture permeability of the first cured layer constituting the iodine-based polarizer side of the adhesive layer designed in a two-layer structure is 150 g / m². 2 When the incubation period is 24 hours or less, the hydrophobicity of the adhesive layer on the iodine-based polarizer side increases further, resulting in a particularly improved barrier function against the iodine-based polarizer. Therefore, it is preferable that the adhesive layer improves two or more functions in a more balanced manner.

[0048] <First adhesive composition> The monomer components constituting the first adhesive composition can be used without particular limitation as long as their logPow, calculated by the weighted average of mole fractions, is 2.5 or higher. However, in order to more effectively exhibit the barrier function against iodine-based polarizers, it is preferable that the first adhesive composition contains at least a (meth)acrylate compound and a photopolymerization initiator, and that the (meth)acrylate compound contains (meth)acrylate(A) having a cyclic hydrocarbon skeleton in its molecule. Furthermore, it is more preferable that, when the total amount of the (meth)acrylate compound is 100 parts by mass, it contains 70 parts by mass or more of (meth)acrylate(A) having a cyclic hydrocarbon skeleton in its molecule. The first adhesive composition used in the present invention is preferably a radical polymerizable adhesive composition using a photopolymerization initiator. Specifically, it is preferable that it is a radical polymerizable adhesive composition capable of forming an adhesive layer by photo-radical polymerization of the (meth)acrylate compound using a photopolymerization initiator.

[0049] The (meth)acrylate (A) having a cyclic hydrocarbon skeleton is, for example, a (meth)acrylate having an alicyclic skeleton, and due to having a cyclic hydrocarbon skeleton, it can form an adhesive layer with low mobility and low ion permeability. Therefore, the movement of iodine from the iodine-based polarizer can be retained in the adhesive layer. As a result, even when an image display device incorporating the laminated optical film according to the present invention is used under high temperature and high humidity conditions, corrosion of the panel or sensor of the image display device by iodine can be sufficiently prevented. The (meth)acrylate (A) is preferably a compound having 5 to 12 carbon atoms constituting the cyclic hydrocarbon skeleton in the molecule, because it can more reliably retain the movement of iodine from the iodine-based polarizer in the adhesive layer.

[0050] In the present invention, it is preferable to use a (meth)acrylate (A) having a cyclic hydrocarbon skeleton that has at least two functionalities, because it can more reliably retain the movement of iodine from the iodine-based polarizer within the adhesive. Examples of two- or more functional (meth)acrylates include the compound described in formula (A1) below, which will be described later.

[0051] In this invention, the (meth)acrylate (A) having a cyclic hydrocarbon skeleton is defined as follows: (A1) to (A4); [ka] It is preferable to use at least one compound selected from the group consisting of the compounds described in [reference] because it can more reliably retain the movement of iodine from the iodine-based polarizer within the adhesive layer.

[0052] From the viewpoint of providing a barrier function against iodine in the adhesive layer, the adhesive composition used in the present invention preferably contains 70 parts by mass or more of (meth)acrylate (A) having a cyclic hydrocarbon skeleton in its molecule, when the total amount of (meth)acrylate compounds is 100 parts by mass. More preferably, it contains 80 parts by mass or more, and even more preferably, 85 parts by mass or more.

[0053] In the present invention, it is preferable that the first adhesive composition used further contains (meth)acrylate (B) containing a hydroxyl group. The (meth)acrylate (B) containing a hydroxyl group has the effect of enhancing the adhesion function of the first adhesive layer to the iodine-based polarizer. For this reason, in the laminated optical film according to the present invention, it is preferable that the first adhesive layer on the polarizer side is formed by a cured layer of the first adhesive composition containing (meth)acrylate (A) having a cyclic hydrocarbon skeleton in the molecule and (meth)acrylate (B) containing a hydroxyl group, because both the barrier function of the adhesive layer and the adhesion function of the adhesive layer to the iodine-based polarizer can be achieved. However, in order to achieve both the barrier function of the adhesive layer, particularly the first adhesive layer, and the adhesion function of the adhesive layer, particularly the first adhesive layer, to the iodine-based polarizer, it is preferable that when the total amount of (meth)acrylate compounds in the first adhesive composition is 100 parts by mass, the amount of (meth)acrylate (A) having a cyclic hydrocarbon skeleton in its molecule is 70 parts by mass or more, and furthermore, the content of (meth)acrylate (A) relative to (meth)acrylate (B) is designed to be within the range of 2 to 6 times. To further effectively achieve both the barrier function of the first adhesive layer and the adhesion function of the first adhesive layer to the iodine-based polarizer, it is even more preferable that when the total amount of (meth)acrylate compounds is 100 parts by mass, the amount of (meth)acrylate (B) is 5 to 25 parts by mass.

[0054] Examples of hydroxyl group-containing (meth)acrylates (B) include hydroxyalkyl (meth)acrylates such as 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, 6-hydroxyhexyl (meth)acrylate, 8-hydroxyoctyl (meth)acrylate, 10-hydroxydecyl (meth)acrylate, and 12-hydroxylauryl (meth)acrylate; hydroxyl group-containing (meth)acrylates such as [4-(hydroxymethyl)cyclohexyl]methyl acrylate, cyclohexanedimethanol mono(meth)acrylate, and 2-hydroxy-3-phenoxypropyl (meth)acrylate; and N-hydroxyalkyl group-containing (meth)acrylamide derivatives such as N-methylol (meth)acrylamide, N-hydroxyethyl (meth)acrylamide, and N-methylol-N-propane (meth)acrylamide.

[0055] In addition to (meth)acrylate (A) having a cyclic hydrocarbon skeleton in its molecule and (meth)acrylate (B) containing a hydroxyl group, the first adhesive composition used in the present invention may also contain active energy ray curable polymerizable compounds such as electron beam curable, ultraviolet curable, and visible light curable compounds. Active energy ray curable polymerizable compounds can be classified into radical polymerizable compounds and cationic polymerizable compounds. In the present invention, active energy rays with a wavelength range of 10 nm to less than 380 nm are referred to as ultraviolet rays, and active energy rays with a wavelength range of 380 nm to 800 nm are referred to as visible light.

[0056] Radical polymerizable compounds include compounds having a radically polymerizable functional group of a carbon-carbon double bond, such as a (meth)acrylic group or a vinyl group. These monomer components can be either monofunctional radical polymerizable compounds or polyfunctional radical polymerizable compounds having two or more polymerizable functional groups. Furthermore, these radical polymerizable compounds can be used individually or in combination of two or more. Among these radical polymerizable compounds, compounds having a (meth)acrylic group are preferred, for example.

[0057] Examples of monofunctional radical polymerizable compounds include (meth)acrylic acid derivatives. Examples of (meth)acrylic acid derivatives include alkoxy group or phenoxy group-containing (meth)acrylates such as 2-methoxyethyl (meth)acrylate, 2-ethoxyethyl (meth)acrylate, 2-methoxymethoxyethyl (meth)acrylate, 3-methoxybutyl (meth)acrylate, ethyl carbitol (meth)acrylate, phenoxyethyl (meth)acrylate, alkylphenoxy polyethylene glycol (meth)acrylate; cyclohexyl (meth)acrylate, 4-tert-butylcyclohexyl acrylate, and cyclopentyl Examples include cycloalkyl(meth)acrylates such as (meth)acrylate; aralkyl(meth)acrylates such as benzyl(meth)acrylate; polycyclic(meth)acrylates such as 2-isobornyl(meth)acrylate, 2-norbornylmethyl(meth)acrylate, 5-norbornen-2-ylmethyl(meth)acrylate, 3-methyl-2-norbornylmethyl(meth)acrylate, dicyclopentenyl(meth)acrylate, dicyclopentenyloxyethyl(meth)acrylate, and dicyclopentanyl(meth)acrylate.

[0058] Other examples of monofunctional radical polymerizable compounds include various (meth)acrylic acid derivatives having a (meth)acryloyloxy group. Specifically, examples include alkyl esters of (meth)acrylic acid (with 1-20 carbon atoms), such as methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, 2-methyl-2-nitropropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, s-butyl (meth)acrylate, t-butyl (meth)acrylate, n-pentyl (meth)acrylate, t-pentyl (meth)acrylate, 3-pentyl (meth)acrylate, 2,2-dimethylbutyl (meth)acrylate, n-hexyl (meth)acrylate, cetyl (meth)acrylate, n-octyl (meth)acrylate, lauryl (meth)acrylate, 2-ethylhexyl (meth)acrylate, 4-methyl-2-propylpentyl (meth)acrylate, and n-octadecyl (meth)acrylate.

[0059] Other monofunctional radical polymerizable compounds include, for example, (meth)acrylamide derivatives having a (meth)acrylamide group. Specific examples of (meth)acrylamide derivatives include, for example, N-alkyl group-containing (meth)acrylamide derivatives such as N-methyl(meth)acrylamide, N,N-dimethyl(meth)acrylamide, N,N-diethyl(meth)acrylamide, N-isopropyl(meth)acrylamide, N-butyl(meth)acrylamide, and N-hexyl(meth)acrylamide; N-aminoalkyl group-containing (meth)acrylamide derivatives such as aminomethyl(meth)acrylamide and aminoethyl(meth)acrylamide; N-alkoxy group-containing (meth)acrylamide derivatives such as N-methoxymethylacrylamide and N-ethoxymethylacrylamide; and N-mercaptoalkyl group-containing (meth)acrylamide derivatives such as mercaptomethyl(meth)acrylamide and mercaptoethyl(meth)acrylamide. Furthermore, examples of heterocyclic (meth)acrylamide derivatives in which the nitrogen atom of the (meth)acrylamide group forms a heterocycle include N-acryloylmorpholine, N-acryloylpiperidine, N-methacryloylpiperidine, and N-acryloylpyrrolidine.

[0060] Furthermore, monofunctional radical polymerizable compounds include epoxy group-containing (meth)acrylates such as glycidyl (meth)acrylate and 4-hydroxybutyl (meth)acrylate glycidyl ether; halogen-containing (meth)acrylates such as 2,2,2-trifluoroethyl (meth)acrylate, 2,2,2-trifluoroethyl ethyl (meth)acrylate, tetrafluoropropyl (meth)acrylate, hexafluoropropyl (meth)acrylate, octafluoropentyl (meth)acrylate, heptadecafluorodecyl (meth)acrylate, and 3-chloro-2-hydroxypropyl (meth)acrylate; and dimethylaminoethyl (meth)acrylate, etc. Alkylaminoalkyl (meth)acrylates; oxetane group-containing (meth)acrylates such as 3-oxetanylmethyl (meth)acrylate, 3-methyl-oxetanylmethyl (meth)acrylate, 3-ethyl-oxetanylmethyl (meth)acrylate, 3-butyl-oxetanylmethyl (meth)acrylate, and 3-hexyl-oxetanylmethyl (meth)acrylate; heterocyclic (meth)acrylates such as tetrahydrofurfuryl (meth)acrylate and butyrolactone (meth)acrylate; or hydroxypivalate neopentyl glycol (meth)acrylic acid adducts and p-phenylphenol (meth)acrylate may be used.

[0061] Furthermore, as monofunctional radical polymerizable compounds, carboxyl group-containing monomers such as (meth)acrylic acid, carboxyethyl acrylate, carboxypentyl acrylate, itaconic acid, maleic acid, fumaric acid, crotonic acid, and isocrotonic acid may be used.

[0062] Furthermore, as monofunctional radical polymerizable compounds, for example, lactam-based vinyl monomers such as N-vinylpyrrolidone, N-vinyl-ε-caprolactam, and methylvinylpyrrolidone; and vinyl monomers having nitrogen-containing heterocyclic rings such as vinylpyridine, vinylpiperidone, vinylpyrimidine, vinylpiperazine, vinylpyrazine, vinylpyrrole, vinylimidazole, vinyloxazole, and vinylmorpholine may be used.

[0063] Furthermore, as the monofunctional radical polymerizable compound, a radical polymerizable compound having an active methylene group may be used. A radical polymerizable compound having an active methylene group is a compound that has an active double bond group such as a (meth)acrylic group at its terminal or in the molecule, and also has an active methylene group. Examples of active methylene groups include an acetoacetyl group, an alkoxymalonyl group, or a cyanoacetyl group. It is preferable that the active methylene group is an acetoacetyl group. Specific examples of radical polymerizable compounds having an active methylene group include acetoacetoxyalkyl (meth)acrylates such as 2-acetoacetoxyethyl (meth)acrylate, 2-acetoacetoxypropyl (meth)acrylate, and 2-acetoacetoxy-1-methylethyl (meth)acrylate; 2-ethoxymalonyloxyethyl (meth)acrylate, 2-cyanoacetoxyethyl (meth)acrylate, N-(2-cyanoacetoxyethyl)acrylamide, N-(2-propionylacetoxybutyl)acrylamide, N-(4-acetoacetoxymethylbenzyl)acrylamide, and N-(2-acetoacetylaminoethyl)acrylamide. The radical polymerizable compound having an active methylene group is preferably an acetoacetoxyalkyl (meth)acrylate.

[0064] Furthermore, in the present invention, the first adhesive composition contains the following general formula (1): [ka] A monofunctional radical polymerizable compound represented by (where X is a reactive group, Y is a C1-C12 alkylene group which may have a branched chain, or a phenylene group which may have a substituent, R 1 and R 2 Each of these may independently represent a hydrogen atom, an aliphatic hydrocarbon group which may have substituents, an aryl group, or a heterocyclic group.

[0065] In the monofunctional radically polymerizable compound represented by the general formula (1), examples of the aliphatic hydrocarbon group include a linear or branched alkyl group having 1 to 20 carbon atoms which may have a substituent, a cyclic alkyl group having 3 to 20 carbon atoms which may have a substituent, and an alkenyl group having 2 to 20 carbon atoms. Examples of the aryl group include a phenyl group having 6 to 20 carbon atoms which may have a substituent, a naphthyl group having 10 to 20 carbon atoms which may have a substituent, and the like. Examples of the heterocyclic group include a 5-membered or 6-membered group which contains at least one hetero atom and may have a substituent. These may be linked to each other to form a ring. In the general formula (1), R 1 and R 2 are preferably a hydrogen atom, a linear or branched alkyl group having 1 to 3 carbon atoms, and most preferably a hydrogen atom.

[0066] In the monofunctional radical polymerizable compound represented by general formula (1), X is a reactive group that can react with the curable components constituting the adhesive layer. Examples include hydroxyl groups, amino groups, aldehyde groups, carboxyl groups, vinyl groups, (meth)acrylic groups, styryl groups, (meth)acrylamide groups, vinyl ether groups, epoxy groups, oxetane groups, α,β-unsaturated carbonyl groups, mercapto groups, halogen groups, and the like. When the curable adhesive composition constituting the adhesive layer is curable by active energy rays, the reactive group X is preferably at least one reactive group selected from the group consisting of vinyl group, (meth)acrylic group, styryl group, (meth)acrylamide group, vinyl ether group, epoxy group, oxetane group, and mercapto group. When the curable adhesive composition constituting the adhesive layer is radical polymerizable, the reactive group X is preferably at least one reactive group selected from the group consisting of (meth)acrylic group, styryl group, and (meth)acrylamide group. When the monofunctional radical polymerizable compound represented by general formula (1) has a (meth)acrylamide group, it is more preferable because it is highly reactive and increases the copolymerization rate with the curable component in the adhesive layer. Furthermore, it is also preferable because the (meth)acrylamide group has high polarity and excellent adhesive properties, which allows the effects of the present invention to be obtained efficiently. When the curable adhesive composition constituting the adhesive layer is cationic polymerizable, the reactive group X preferably has at least one functional group selected from hydroxyl group, amino group, aldehyde, carboxyl group, vinyl ether group, epoxy group, oxetane group, and mercapto group. In particular, the presence of an epoxy group is preferred because it provides excellent adhesion between the resulting adhesive layer and the adherend, and the presence of a vinyl ether group is preferred because it provides excellent curability of the curable adhesive composition.

[0067] Preferred specific examples of monofunctional radical polymerizable compounds represented by general formula (1) include the following compounds (1a) to (1d). Note that R in general formulas (1a) and (1b) 3 This is either a hydrogen atom or a methyl group. [ka]

[0068] Examples of monofunctional radical polymerizable compounds represented by general formula (1) include, in addition to the examples given above, esters of (meth)acrylates and boric acid, such as esters of hydroxyethyl acrylamide and boric acid, methylol acrylamide and boric acid, esters of hydroxyethyl acrylate and boric acid, and esters of hydroxybutyl acrylate and boric acid.

[0069] Examples of polyfunctional radical polymerizable compounds having two or more polymerizable functional groups include tripropylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, polyethylene glycol diacrylate, 1,6-hexanediol di(meth)acrylate, 1,9-nonanediol di(meth)acrylate, 1,10-decanediol diacrylate, 2-ethyl-2-butylpropanediol di(meth)acrylate, bisphenol A di(meth)acrylate, bisphenol A ethylene oxide adduct di(meth)acrylate, bisphenol A propylene oxide adduct di(meth)acrylate, bisphenol A diglycidyl ether di(meth)acrylate, and Examples include esters of (meth)acrylic acid with polyhydric alcohols such as opentyl glycol di(meth)acrylate, tricyclodecane dimethanol di(meth)acrylate, cyclic trimethylolpropane formal(meth)acrylate, dioxane glycol di(meth)acrylate, trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, dipentaerythritol penta(meth)acrylate, dipentaerythritol hexa(meth)acrylate, and EO-modified diglycerin tetra(meth)acrylate, as well as 9,9-bis[4-(2-(meth)acryloyloxyethoxy)phenyl]fluorene. Specific examples include Light Acrylate 9EG-A (manufactured by Kyoeisha Chemical Co., Ltd.), Aronics M-220 (manufactured by Toagosei Co., Ltd.), Light Acrylate 1,9ND-A (manufactured by Kyoeisha Chemical Co., Ltd.), Light Acrylate DGE-4A (manufactured by Kyoeisha Chemical Co., Ltd.), Light Acrylate DCP-A (manufactured by Kyoeisha Chemical Co., Ltd.), SR-531 (manufactured by Sartomer), CD-536 (manufactured by Sartomer), and others.

[0070] In the present invention, the first adhesive composition may contain, in addition to the radical polymerizable compound, an acrylic oligomer obtained by polymerizing (meth)acrylic monomer and having no polymerizable groups. By including the acrylic oligomer in the first adhesive composition, curing shrinkage when the composition is irradiated and cured with active energy rays can be reduced, and the interfacial stress between the first adhesive layer and the iodine-based polarizer can be reduced. As a result, a decrease in the adhesion between the first adhesive layer and the iodine-based polarizer can be suppressed.

[0071] The first adhesive composition is preferably low viscosity when considering workability and uniformity during coating, and is therefore preferably made by polymerizing (meth)acrylic monomers, and the acrylic oligomer without polymerizable groups is also preferably low viscosity. As an acrylic oligomer that is low viscosity and can prevent curing shrinkage of the adhesive layer, it is preferable that the weight-average molecular weight (Mw) is 15,000 or less, more preferably 10,000 or less, and particularly preferably 5,000 or less. On the other hand, in order to sufficiently suppress curing shrinkage of the cured product layer (adhesive layer), it is preferable that the weight-average molecular weight (Mw) of the acrylic oligomer is 500 or more, more preferably 1,000 or more, and particularly preferably 1,500 or more. Examples of (meth)acrylic monomers that constitute acrylic oligomers include, specifically, methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, 2-methyl-2-nitropropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, S-butyl (meth)acrylate, t-butyl (meth)acrylate, n-pentyl (meth)acrylate, t-pentyl (meth)acrylate, 3-pentyl (meth)acrylate, 2,Alkyl esters of (meth)acrylic acid (C1-C20) such as 2-dimethylbutyl (meth)acrylate, n-hexyl (meth)acrylate, cetyl (meth)acrylate, n-octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, 4-methyl-2-propylpentyl (meth)acrylate, N-octadecyl (meth)acrylate, and also, for example, cycloalkyl (meth)acrylates (e.g., cyclohexyl (meth)acrylate, cyclopentyl (meth)acrylate, etc.), aralkyl (meth)acrylates (e.g., benzyl (meth)acrylate, etc.), polycyclic (meth)acrylates (e.g., 2-isobornyl (meth)acrylate, 2-norbornylmethyl (meth)acrylate, 5-norbornen-2-yl-methyl (meth)acrylate, 3-methyl-2-norbornylmethyl ( (meth)acrylates, etc.), hydroxyl group-containing (meth)acrylic acid esters (e.g., hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 2,3-dihydroxypropylmethyl-butyl (meth)methacrylate, etc.), alkoxy group- or phenoxy group-containing (meth)acrylic acid esters (2-methoxyethyl (meth)acrylate, 2-ethoxyethyl (meth)acrylate, 2-methoxymethoxyethyl (meth)acrylate, 3-methoxybutyl (meth)acrylate, ethyl carbitol (meth)acrylate, phenoxyethyl (meth)acrylate, etc.), epoxy group-containing (meth)acrylic acid esters (e.g., glycidyl (meth)acrylate, etc.), halogen-containing (meth)acrylic acid esters (e.g., 2,2,2-trifluoroethyl (meth)acrylate, 2,2Examples include 2-trifluoroethylethyl (meth)acrylate, tetrafluoropropyl (meth)acrylate, hexafluoropropyl (meth)acrylate, octafluoropentyl (meth)acrylate, heptadecafluorodecyl (meth)acrylate, etc., and alkylaminoalkyl (meth)acrylates (e.g., dimethylaminoethyl (meth)acrylate). These (meth)acrylates can be used alone or in combination of two or more types. Specific examples of acrylic oligomers (E) include "ARUFON" from Toagosei Co., Ltd., "Actflow" from Soken Chemical Co., Ltd., and "JONCRYL" from BASF Japan.

[0072] When using radical polymerizable compounds, the photopolymerization initiator is appropriately selected based on the active energy ray. When curing is performed using ultraviolet or visible light, a photopolymerization initiator that undergoes ultraviolet or visible light cleavage is used. Examples of such photopolymerization initiators include benzophenone compounds such as benzyl, benzophenone, benzoylbenzoic acid, and 3,3'-dimethyl-4-methoxybenzophenone; aromatic ketone compounds such as 4-(2-hydroxyethoxy)phenyl(2-hydroxy-2-propyl)ketone, α-hydroxy-α,α'-dimethylacetophenone, 2-methyl-2-hydroxypropiophenone, and α-hydroxycyclohexylphenyl ketone; acetophenone compounds such as methoxyacetophenone, 2,2-dimethoxy-2-phenylacetophenone, 2,2-diethoxyacetophenone, and 2-methyl-1-[4-(methylthio)-phenyl]-2-morpholinopropan-1-one; and benzoin methyl ether, benzoin ethyl ether, and benzoin isopropyl ether. Examples include benzoin ether compounds such as benzoin butyl ether and anisoin methyl ether; aromatic ketal compounds such as benzyldimethyl ketal; aromatic sulfonyl chloride compounds such as 2-naphthalenesulfonyl chloride; photoactive oxime compounds such as 1-phenone-1,1-propanedione-2-(o-ethoxycarbonyl)oxime; thioxanthone compounds such as thioxanthone, 2-chlorothioxanthone, 2-methylthioxanthone, 2,4-dimethylthioxanthone, isopropylthioxanthone, 2,4-dichlorothioxanthone, 2,4-diethylthioxanthone, 2,4-diisopropylthioxanthone, and dodecylthioxanthone; camphorquinone; halogenated ketones; acylphosphinoxides; and acylphosphonates.

[0073] The amount of the photopolymerization initiator is 20% by weight or less when the total amount of the first adhesive composition is considered to be 100% by weight. Preferably, the amount of the photopolymerization initiator is 0.01 to 20% by weight, more preferably 0.05 to 10% by weight, and more preferably 0.1 to 5% by weight.

[0074] Furthermore, when using an adhesive composition that contains a radical polymerizable compound as a curing component and is curable with visible light, it is particularly preferable to use a photopolymerization initiator that is highly sensitive to light of 380 nm or higher. Photopolymerization initiators that are highly sensitive to light of 380 nm or higher will be described later.

[0075] The aforementioned photopolymerization initiator is a compound represented by the following general formula (2);

[0076] [ka] (In the formula, R 1 and R 2 R represents -H, -CH2CH3, -iPr, or Cl. 1 and R 2 It is preferable to use the compound represented by general formula (2) alone (which may be the same or different) or to use it in combination with a photopolymerization initiator that is highly sensitive to light of 380 nm or higher, as described later. When the compound represented by general formula (2) is used, the adhesion is superior to when the photopolymerization initiator that is highly sensitive to light of 380 nm or higher is used alone. Among the compounds represented by general formula (2), R 1 and R 2 Diethylthioxanthone, in which is -CH2CH3, is particularly preferred. The composition ratio of the compound represented by general formula (2) in the adhesive composition is preferably 0.1 to 5 parts by weight, more preferably 0.5 to 4 parts by weight, and even more preferably 0.9 to 3 parts by weight, based on 100 parts by weight of the total amount of curable components.

[0077] Furthermore, it is preferable to add polymerization initiators as needed. Examples of polymerization initiators include triethylamine, diethylamine, N-methyldiethanolamine, ethanolamine, 4-dimethylaminobenzoic acid, methyl 4-dimethylaminobenzoate, ethyl 4-dimethylaminobenzoate, and isoamyl 4-dimethylaminobenzoate, with ethyl 4-dimethylaminobenzoate being particularly preferred. When using polymerization initiators, the amount added is usually 0 to 5 parts by weight, preferably 0 to 4 parts by weight, and most preferably 0 to 3 parts by weight, per 100 parts by weight of the total amount of curable components.

[0078] Furthermore, known photopolymerization initiators can be used in combination as needed. Since transparent protective films with UV absorption ability do not transmit light below 380 nm, it is preferable to use a photopolymerization initiator that is highly sensitive to light above 380 nm. Specifically, examples include 2-methyl-1-(4-methylthiophenyl)-2-morpholinopropan-1-one, 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1, 2-(dimethylamino)-2-[(4-methylphenyl)methyl]-1-[4-(4-morpholinyl)phenyl]-1-butanone, 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide, and bis(η5-2,4-cyclopentadien-1-yl)-bis(2,6-difluoro-3-(1H-pyrrole-1-yl)-phenyl)titanium.

[0079] In particular, as a photopolymerization initiator, in addition to the photopolymerization initiator of general formula (2), a compound represented by the following general formula (3);

[0080] [ka] (In the formula, R 3 , R 4 and R 5 R represents -H, -CH3, -CH2CH3, -iPr, or Cl. 3 , R 4 and R5 It is preferable to use compounds that are the same or different. As compounds represented by general formula (3), commercially available products such as 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide (trade name: Omnirad819, manufacturer: IGM Resins BV) and 2-methyl-1-(4-methylthiophenyl)-2-morpholinopropan-1-one (trade name: Omnirad907, manufacturer: IGM Resins BV) can be suitably used. In addition, 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1 (trade name: Omnirad369, manufacturer: IGM Resins BV) and 2-(dimethylamino)-2-[(4-methylphenyl)methyl]-1-[4-(4-morpholinyl)phenyl]-1-butanone (trade name: Omnirad379, manufacturer: IGM Resins BV) are preferred due to their high sensitivity.

[0081] In the present invention, it is preferable to use a hydroxyl group-containing photopolymerization initiator among the above-mentioned photopolymerization initiators. When the active energy ray-curable adhesive composition contains a hydroxyl group-containing photopolymerization initiator as a polymerization initiator, the solubility in the adhesive layer with a high concentration of component A on the polarizer side increases, and the curability of the adhesive layer increases. Examples of photopolymerization initiators having a hydroxyl group include 2-methyl-2-hydroxypropiophenone (trade name "DAROCUR1173", manufactured by BASF), 1-hydroxycyclohexylphenyl ketone (trade name "IRGACURE184", manufactured by BASF), 1-[4-(2-hydroxyethoxy)-phenyl]-2-hydroxy-2-methyl-1-propan-1-one (trade name "IRGACURE2959", manufactured by BASF), and 2-hydroxy-1-{4-[4-(2-hydroxy-2-methylpropionyl)-benzyl]phenyl}-2-methyl-propan-1-one (trade name "IRGACURE127", manufactured by BASF). 1-hydroxycyclohexylphenyl ketone is particularly preferred because of its excellent solubility in adhesive layers with a high concentration of component A.

[0082] In the present invention, the first adhesive composition may contain cationic polymerizable compounds in addition to (meth)acrylate (A) having a cyclic hydrocarbon skeleton in its molecule and (meth)acrylate (B) containing a hydroxyl group. Cationic polymerizable compounds are classified into monofunctional cationic polymerizable compounds having one cationic polymerizable functional group in its molecule and polyfunctional cationic polymerizable compounds having two or more cationic polymerizable functional groups in its molecule. Monofunctional cationic polymerizable compounds have relatively low liquid viscosity, so including them in the adhesive composition can reduce the liquid viscosity of the first adhesive composition. Furthermore, monofunctional cationic polymerizable compounds often have functional groups that exhibit various functions, so including them in the first adhesive composition can allow the cured product to exhibit various functions. Polyfunctional cationic polymerizable compounds can cause three-dimensional crosslinking of the cured product of the cationic polymerizable adhesive composition.

[0083] Cationic polymerizable functional groups include epoxy groups, oxetanyl groups, and vinyl ether groups. Compounds containing epoxy groups include aliphatic epoxy compounds, alicyclic epoxy compounds, and aromatic epoxy compounds. Examples of alicyclic epoxy compounds include 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, caprolactone-modified, trimethylcaprolactone-modified, and valerolactone-modified 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, and specifically, Celoxide 2021, Celoxide 2021A, Celoxide 2021P, Celoxide 2081, Celoxide 2083, Celoxide 2085 (all manufactured by Daicel Chemical Industries, Ltd.), and Cyracure UVR-6105, Cyracure UVR-6107, Cyracure 30, R-6110 (all manufactured by Dow Chemical Japan Ltd.). Compounds containing an oxetanyl group have the effect of improving the curability of cationic polymerizable adhesive compositions and reducing the liquid viscosity of the composition, therefore, they contain It is preferable to include them. Examples of compounds having an oxetanyl group include 3-ethyl-3-hydroxymethyloxetane, 1,4-bis[(3-ethyl-3-oxetanyl)methoxymethyl]benzene, 3-ethyl-3-(phenoxymethyl)oxetane, di[(3-ethyl-3-oxetanyl)methyl]ether, 3-ethyl-3-(2-ethylhexyloxymethyl)oxetane, and phenol novolac oxetane. Aronoxetane OXT-101, Aronoxetane OXT-121, Aronoxetane OXT-211, Aronoxetane OXT-221, Aronoxetane OXT-212 (all manufactured by Toagosei Co., Ltd.) are commercially available. Compounds having a vinyl ether group are preferable to include because they have the effect of improving the curability of the cationic polymerizable adhesive composition and reducing the liquid viscosity of the composition.Compounds having a vinyl ether group include 2-hydroxyethyl vinyl ether, diethylene glycol monovinyl ether, 4-hydroxybutyl vinyl ether, diethylene glycol monovinyl ether, triethylene glycol divinyl ether, cyclohexanedimethanol divinyl ether, cyclohexanedimethanol monovinyl ether, tricyclodecane vinyl ether, cyclohexyl vinyl ether, methoxyethyl vinyl ether, ethoxyethyl vinyl ether, and pentaerythritol-type tetravinyl ether.

[0084] In the adhesive layers of the laminated optical film according to the present invention, the second adhesive layer on the optical film side is formed from the second cured layer of the second adhesive composition. The logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of the monomer components contained in the second adhesive composition, is designed to be less than 2.5.

[0085] <Second adhesive composition> The monomer components constituting the second adhesive composition are not particularly limited as long as the logPow calculated by the weighted average of mole fractions is less than 2.5, and can be appropriately selected and used from among the monomer components exemplified as constituting the first adhesive composition.

[0086] The laminated optical film according to the present invention has an iodine-based polarizer and an optical film laminated with an adhesive layer in between. As shown in Figure 1, the laminated optical film according to the present invention may also have a transparent protective film laminated on the outer surface (visible surface) of the iodine-based polarizer with a third adhesive layer in between.

[0087] <Transparent protective film> As materials constituting the transparent protective film, for example, thermoplastic resins that are excellent in transparency, mechanical strength, thermal stability, moisture barrier properties, and isotropy are used. Specific examples of such thermoplastic resins include cellulose resins such as triacetylcellulose, polyester resins, polyethersulfone resins, polysulfone resins, polycarbonate resins, polyamide resins, polyimide resins, polyolefin resins, (meth)acrylic resins, cyclic polyolefin resins (norbornene-based resins), polyarylate resins, polystyrene resins, polyvinyl alcohol resins, and mixtures thereof. The transparent protective film may contain one or more suitable additives. Examples of additives include ultraviolet absorbers, antioxidants, lubricants, plasticizers, mold release agents, color inhibitors, flame retardants, nucleating agents, antistatic agents, pigments, and colorants. The content of the above thermoplastic resin in the transparent protective film is preferably 50 to 100% by weight, more preferably 50 to 99% by weight, even more preferably 60 to 98% by weight, and particularly preferably 70 to 97% by weight. If the content of the above-mentioned thermoplastic resin in the transparent protective film is 50% by weight or less, the high transparency and other properties inherent to the thermoplastic resin may not be fully realized.

[0088] Furthermore, the material used to form the transparent protective film is preferably one that is excellent in terms of transparency, mechanical strength, thermal stability, moisture barrier properties, and isotropy, and is particularly good if it has a moisture permeability of 150 g / m². 2 It is more preferable that the amount is 24 hours or less, and 140 g / m² 2 Products with a shelf life of 24 hours or less are particularly preferred, and 120 g / m² 2 Even better are those with a shelf life of 24 hours or less.

[0089] The transparent protective film may be provided with functional layers such as a hard coat layer, an anti-reflective layer, an anti-sticking layer, a diffusion layer, or an anti-glare layer. These functional layers, such as the hard coat layer, anti-reflective layer, anti-sticking layer, diffusion layer, and anti-glare layer, can be provided on the transparent protective film itself, or they can be provided separately from the transparent protective film.

[0090] The thickness of the transparent protective film can be determined as appropriate, but generally it is about 1 to 500 μm, preferably 1 to 300 μm, and more preferably 5 to 200 μm, considering factors such as strength, workability, and thinness. Furthermore, 10 to 200 μm is preferred, and 20 to 80 μm is preferred.

[0091] <Third adhesive layer> The third adhesive layer may be formed by a cured layer of monomer components that can constitute the first adhesive composition described above. Alternatively, it may be formed by a radical polymerizable adhesive composition, a cationic polymerizable adhesive composition, or an aqueous adhesive composition known to those skilled in the art. As the aqueous adhesive composition, an aqueous solution (for example, solid content concentration of 0.5 to 60% by weight) of an aqueous adhesive such as an isocyanate adhesive, a polyvinyl alcohol adhesive, a gelatin adhesive, a vinyl latex adhesive, or an aqueous polyester adhesive is preferably used. From the viewpoint of thinning, the thickness of the third adhesive layer is preferably 0.1 to 5 μm.

[0092] The laminated optical film according to the present invention has an adhesive layer on the phase difference film side and is bonded to an organic light-emitting diode panel or a touch sensor.

[0093] <Adhesive layer> The adhesive forming the adhesive layer is not particularly limited, but for example, adhesives based on polymers such as acrylic polymers, silicone polymers, polyesters, polyurethanes, polyamides, polyethers, fluorine-based or rubber-based polymers can be appropriately selected and used. In particular, adhesives that have excellent optical transparency, exhibit appropriate wettability, cohesiveness and adhesion properties, and have excellent weather resistance and heat resistance, such as acrylic adhesives, are preferably used.

[0094] For the exposed surface of the adhesive layer, a separator is temporarily attached and covered to prevent contamination until it is put into practical use. This prevents contact with the adhesive layer under normal handling conditions. As for the separator, except for the thickness conditions mentioned above, suitable thin materials such as plastic film, rubber sheet, paper, cloth, nonwoven fabric, net, foam sheet, metal foil, or laminates thereof can be used, and may be coated with a suitable release agent such as silicone-based, long-chain alkyl-based, fluorine-based, or molybdenum sulfide as needed, in accordance with conventional methods.

[0095] In the present invention, the laminated optical film can be manufactured by the following manufacturing method. A method for manufacturing a laminated optical film in which at least an iodine-based polarizing film and an optical film are laminated via an adhesive layer, The adhesive layer has a two-layer structure consisting of a first adhesive layer on the iodine-based polarizer side and a second adhesive layer on the optical film side. The first adhesive layer is formed from the first cured layer of the first adhesive composition, and the logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of the monomer components contained in the first adhesive composition, is 2.5 or greater. The second adhesive layer is formed from the second cured layer of the second adhesive composition, and the logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of the monomer components contained in the second adhesive composition, is less than 2.5. A first coating step of coating the iodine-based polarizer with the first adhesive composition, and a second coating step of coating the optical film with the second adhesive composition, A bonding step of bonding the coated surface of the first adhesive composition of the iodine-based polarizer and the coated surface of the second adhesive composition of the optical film, A method for manufacturing a laminated optical film, comprising an bonding step of bonding the iodine-based polarizer and the optical film via an adhesive layer formed by irradiating at least the first adhesive composition and the second adhesive composition with active energy rays from the iodine-based polarizer side or the optical film side to cure them. Each step is described below.

[0096] (Coating process) In the first coating step, which involves coating an iodine-based polarizer with a first adhesive composition, and the second coating step, which involves coating an optical film with a second adhesive composition, the coating method is appropriately selected depending on the viscosity of the composition and the desired thickness. Examples include reverse coaters, gravure coaters (direct, reverse, and offset), bar reverse coaters, roll coaters, die coaters, bar coaters, and rod coaters. The viscosity of the adhesive composition is preferably 0.1 to 100 mPa·s. If the viscosity of the composition is high, the surface smoothness after coating will be poor, resulting in an undesirable appearance. For this reason, each composition can be heated or cooled to adjust the viscosity to a preferred range before application.

[0097] (Lamination process) The iodine-based polarizer and optical film are bonded together. When bonding the iodine-based polarizer and optical film via the first and second adhesive compositions, a roll laminator or the like is used.

[0098] (Adhesion process) The iodine-based polarizer and the optical film are bonded together via adhesive layers (first cured layer and second cured layer) formed by curing at least the first and second adhesive compositions by irradiating them with active energy rays from either the iodine-based polarizer side or the optical film side. The irradiation direction of the active energy rays (electron beam, ultraviolet light, visible light, etc.) can be any suitable direction.

[0099] When irradiating with an electron beam, any suitable irradiation conditions can be adopted, as long as they are conditions that can cure at least the first and second adhesive compositions. For example, the acceleration voltage for electron beam irradiation is preferably 5kV to 300kV, and more preferably 10kV to 250kV. If the acceleration voltage is less than 5kV, the electron beam may not reach the first and second adhesive compositions, resulting in insufficient curing. If the acceleration voltage exceeds 300kV, the penetration force through the sample may be too strong, potentially damaging the iodine-based polarizer and optical film. The irradiation dose is 5 to 100kGy, more preferably 10 to 75kGy. If the irradiation dose is less than 5kGy, the first and second adhesive compositions will not cure sufficiently. If it exceeds 100kGy, the iodine-based polarizer and optical film will be damaged, resulting in a decrease in mechanical strength and yellowing, making it impossible to obtain the desired optical properties.

[0100] Electron beam irradiation is usually performed in an inert gas environment, but if necessary, it may be performed in air or under conditions with a small amount of oxygen introduced. Depending on the materials of the iodine-based polarizer and optical film, by appropriately introducing oxygen, oxygen inhibition can be intentionally caused on the iodine-based polarizer surface and optical film surface that are first struck by the electron beam, thereby preventing damage to the iodine-based polarizer and optical film layer, and allowing the electron beam to be efficiently irradiated only to the first and second adhesive compositions.

[0101] When manufacturing the laminated optical film according to the present invention, it is preferable to use an active energy ray that includes visible light in the wavelength range of 380 nm to 450 nm, and more particularly, an active energy ray that has the highest irradiation amount of visible light in the wavelength range of 380 nm to 450 nm. When manufacturing the laminated optical film according to the present invention, it is preferable to use a gallium-filled metal halide lamp or an LED light source that emits light in the wavelength range of 380 to 440 nm as the active energy ray. Alternatively, a light source containing ultraviolet and visible light such as a low-pressure mercury lamp, medium-pressure mercury lamp, high-pressure mercury lamp, ultra-high-pressure mercury lamp, incandescent bulb, xenon lamp, halogen lamp, carbon arc lamp, metal halide lamp, fluorescent lamp, tungsten lamp, gallium lamp, excimer laser, or sunlight can be used, and it is also possible to use a bandpass filter to block ultraviolet light with wavelengths shorter than 380 nm. To improve the adhesion performance of the adhesive layer between the iodine-based polarizer and the optical film while preventing curling of the laminated optical film, it is preferable to use an active energy ray obtained by using a gallium-filled metal halide lamp and passing it through a bandpass filter capable of blocking light with wavelengths shorter than 380 nm, or to use an active energy ray with a wavelength of 405 nm obtained using an LED light source.

[0102] When manufacturing the laminated optical film according to the present invention in a continuous line, the line speed depends on the curing time of the first adhesive composition and the second adhesive composition, but is preferably 1 to 500 m / min, more preferably 5 to 300 m / min, and even more preferably 10 to 100 m / min. If the line speed is too low, productivity will be poor, or the damage to the iodine-based polarizer and optical film will be too great, making it impossible to produce a laminated optical film that can withstand durability tests. If the line speed is too high, the curing of the first adhesive composition and the second adhesive composition will be insufficient, and the desired adhesion may not be obtained.

[0103] (Laminated optical film) The laminated optical film according to the present invention can be preferably used for forming various image display devices such as organic EL displays and liquid crystal displays. The formation of organic EL displays and liquid crystal displays can be carried out in accordance with conventional methods. That is, liquid crystal displays are generally formed by assembling components such as liquid crystal cells, polarizing films or optical films, and, if necessary, lighting systems, and incorporating drive circuits. However, the present invention is not particularly limited except for the use of the laminated optical film according to the present invention, and can be carried out in accordance with conventional methods. Any type of liquid crystal cell can be used, such as TN type, STN type, or π type.

[0104] Appropriate liquid crystal display devices can be formed, such as liquid crystal display devices in which optical laminates are arranged on one or both sides of a liquid crystal cell, or in which a backlight or reflector is used in the illumination system. In this case, the optical laminate according to the present invention can be installed on one or both sides of the liquid crystal cell. When optical laminates are provided on both sides, they may be the same or different. Furthermore, when forming a liquid crystal display device, appropriate components such as diffusers, anti-glare layers, anti-reflective films, protective plates, prism arrays, lens array sheets, light diffusers, and backlights can be arranged in appropriate positions in one or more layers. [Examples]

[0105] The following describes some embodiments of the present invention, but the embodiments of the present invention are not limited to these.

[0106] <Iodine-based polarizers> A laminate was formed by air-assisted stretching at a stretching temperature of 130°C from an amorphous PET substrate with a 9 μm thick PVA layer. Next, a colored laminate was formed by dyeing the stretched laminate. Furthermore, an optical film laminate containing a 5 μm thick PVA layer was formed by stretching the colored laminate in boric acid water at a stretching temperature of 65°C, integrally with the amorphous PET substrate, to achieve a total stretching ratio of 5.94 times. Through this two-stage stretching, an optical film laminate containing a 5 μm thick PVA layer (iodine-based polarizer) was obtained, in which the PVA molecules of the PVA layer formed on the amorphous PET substrate were highly oriented, and the iodine adsorbed by dyeing was highly oriented in one direction as a polyiodide ion complex, forming a thin polarizer.

[0107] <Photopolymerizable liquid crystal composition> A photopolymerizable liquid crystal compound exhibiting a nematic liquid crystal phase (BASF's "Paliocolor LC242") was dissolved in cyclopentanone to prepare a solution with a solid content of 30% by weight. A surfactant (Bic Chemie's "BYK-360") and a photopolymerization initiator (IGM Resins' "Omnirad907") were added to this solution to prepare a liquid crystal composition solution. The amounts of surfactant and photopolymerization initiator added were 0.01 parts by weight and 3 parts by weight, respectively, per 100 parts by weight of the photopolymerizable liquid crystal compound.

[0108] <Phase difference film> Using a biaxially oriented norbornene-based film (Zeonor Film, manufactured by Zeon Corporation, thickness: 33 μm, frontal retardation: 135 nm) as a substrate, the above liquid crystal composition was coated onto the substrate by a bar coater so that the phase difference was λ / 2, and the liquid crystal was oriented by heating at 100°C for 3 minutes. After cooling to room temperature, the film was subjected to a nitrogen atmosphere with an integrated light intensity of 400 mJ / cm². 2 A laminate was obtained in which a homogeneous oriented liquid crystal layer (a liquid crystal phase difference film) was provided by photocuring by irradiation with ultraviolet light.

[0109] <Laminated Optical Film> The PVA layer surface of an optical film laminate containing a PVA layer (iodine-based polarizer) was treated with a corona treatment machine at a processing density of 50 W·min / m².2 Corona treatment was performed on the corona-treated surface. The first adhesive composition used in Examples 1-4 and Comparative Example 1 was applied to the corona-treated surface to a coating thickness of 2 μm using an MCD coater (manufactured by Fuji Machinery Co., Ltd.) (cell shape: honeycomb, gravure roll line count: 700 lines / inch, opening ratio of cells formed on the gravure roll: 40%, rotation speed 140% / line speed) (first coating step). The coating thickness was measured using a spectroscopic interferometry film thickness meter (manufactured by Ocean Optics: spectrometer "USB2000+", light source "HL-2000", fiber "OCF-103995").

[0110] The materials constituting the first adhesive composition used in Examples 1-4 and Comparative Example 1 are as follows: ((Meth)acrylate(A)) Tricyclodecanedimethanol diacrylate: Trade name "Light Acrylate DCP-A", manufactured by Kyoeisha Chemical Co., Ltd., compound listed in (A-1), logPow value 3.10) • Isobornyl acrylate: Trade name "IB-XA", manufactured by Osaka Organic Chemical Industry Co., Ltd., compound listed in (A-2), logPow value 3.27 ((meth)acrylate(B)) • 4-Hydroxybutyl acrylate: Trade name "4-HBA", manufactured by Osaka Organic Chemical Industry Co., Ltd., logPow value 1.19 (Other monomeric components) • Ditrimethylolpropanetetraacrylate: Product name "Arronix M-408", manufactured by Toagosei Co., Ltd., logPow value 3.85 (Initiator) • Bis(2,4,6-trimethylbenzoyl)phenylphosphine oxide: trade name "Omnirad 819", manufactured by IGM Resins BV. • 1-Hydroxycyclohexyl-phenyl ketone: Trade name "Omnirad 184", manufactured by IGM Resins BV. • 2,4-Diethylthioxanthone: Trade name "DETX-S", manufactured by Nippon Kayaku Co., Ltd.

[0111] For the homogeneous oriented liquid crystal layer (liquid crystal phase difference film) surface of a λ / 2 phase difference film, a corona treatment machine was used to perform a treatment at a density of 50 W·min / m². 2 Corona treatment was performed on the corona-treated surface. The second adhesive composition used in Examples 1-4 and Comparative Example 1 was applied to the corona-treated surface to a coating thickness of 1 μm using an MCD coater (manufactured by Fuji Machinery Co., Ltd.) (cell shape: honeycomb, gravure roll line count: 700 lines / inch, aperture ratio of cells formed on the gravure roll: 40%, rotation speed 140% / line speed) (second coating step). Next, the λ / 2 phase difference film was bonded using a roll machine so that the slow layer axis was at a 15° angle with the transmission axis of the polarizer (bonding step). The bonding line speed was 15 m / min. After that, a visible light irradiation device (Heraeus Light HAMMER10 Mark III, bulb: V bulb, peak illuminance: 1600 mW / cm²) was used from the phase difference film side. 2 Total irradiation dose 1000 / mJ / cm 2 The irradiance and cumulative dose of the active energy rays were measured using a Power Puck 2 (manufactured by EIT, UVV measurement). The adhesive compositions used in Examples 1-4 and Comparative Example 1 were cured by irradiating them with active energy rays, thereby producing a laminated optical film in which a PVA layer (iodine-based polarizer) of an optical film laminate and a phase difference film were laminated via an adhesive layer (cured layers of the first and second adhesive compositions used in Examples 1-4 or Comparative Example 1). The thickness of the first adhesive layer was 2 μm, and the thickness of the second adhesive layer was 1 μm. After the bonding process, the substrate (biaxially oriented norbornene-based film) was peeled off from the phase difference film.

[0112] The materials constituting the first adhesive composition (adhesive (1)) used in Comparative Example 1 and the second adhesive compositions (adhesives (2) to (3)) used in Examples 1 to 4 are as follows. The formulations of adhesives (1) to (3) are shown in Table 1. ((meth)acrylate) • 2-Hydroxyethylacrylamide: Trade name "HEAA", manufactured by KJ Chemicals. • N-Acryloylmorpholin: Trade name "ACMO", manufactured by KJ Chemicals. • Caprolactone-modified acrylate: Product name "Praxel FA1DDM", manufactured by Daicel Corporation • Phenoxydiethylene glycol acrylate: Product name "Light Acrylate P2H-A", manufactured by Kyoeisha Chemical Co., Ltd. • Lauryl acrylate: Product name "Light Acrylate LA", manufactured by Kyoeisha Chemical Co., Ltd. • Isostearyl acrylate: Product name "ISTA", manufactured by Osaka Organic Chemical Industry Co., Ltd. • 1,9-nonanediol diacrylate: Product name "Light Acrylate 1,9ND-A", manufactured by Kyoeisha Chemical Co., Ltd. (Acrylic oligomer) • Acrylic oligomer: Product name "ARFUON UP-1190", manufactured by Toagosei Co., Ltd. (Initiator) • 2-Methyl-1-[4-(methylthio)-phenyl]-2-morpholinopropan-1-one: Trade name "Omnirad 907", manufactured by IGM Resins BV. • 2,4-Diethylthioxanthone: Trade name "DETX-S", manufactured by Nippon Kayaku Co., Ltd.

[0113] [Table 1]

[0114] The moisture permeability, storage modulus (E'), and glass transition temperature (Tg) of the first adhesive layer and second adhesive layer (first cured layer and second cured layer) of the laminated optical films produced in Examples 1-4 and Comparative Example 1 were evaluated by the following methods.

[0115] (Preparation of hardened layer) The prepared adhesive composition was coated onto a cycloolefin polymer (Zeon Corporation, ZF14) to a coating thickness of 100 μm using a wire bar. After irradiation with active energy rays under an inert gas atmosphere, the cured layer was removed from the cycloolefin polymer to obtain a single cured film of the photocurable composition. The active energy ray used was visible light (gallium-filled metal halide lamp). Irradiation device: Light HAMMER10, manufactured by Fusion UV Systems, Inc. Bulb: V-bulb Peak illuminance: 1600 mW / cm 2 Total irradiation dose 1000 / mJ / cm 2 (Wavelengths of 380-440 nm were used.) Illuminance of visible light was measured using a Solatell Sola-Check system.

[0116] (Moisture permeability of the adhesive layer (cured layer)) The moisture permeability test (cup method) was performed in accordance with JIS Z0208. A single hardened film cut to a diameter of 60 mm was placed in a moisture permeability cup containing approximately 150 g of calcium chloride, and the cup was placed in a constant temperature chamber at 40°C and 92% RH humidity for 24 hours. The weight increase of calcium chloride before and after this period was measured to determine the moisture permeability (g / m³). 2 The calculation (24 hours) was performed.

[0117] (Storage modulus (E') of the adhesive layer (cured layer)) The storage modulus (E') was determined from the value of E' at 60°C obtained from dynamic viscoelasticity measurements using a dynamic viscoelasticity measuring device (IT Measurement Control Co., Ltd., product name "DVA-225") under the following conditions. (Load mode): Pulling (Heating rate): 2°C / min (Frequency): 1Hz (Initial distortion): 0.1% (Relative humidity): 90%

[0118] (Glass transition temperature (Tg) of the adhesive layer (cured layer)) The glass transition temperature (Tg) was determined from the peak top temperature of tanδ obtained from dynamic viscoelasticity measurements using a dynamic viscoelasticity measuring device (IT Measurement Control Co., Ltd., product name "DVA-225") under the following conditions. (Load mode): Pulling (Heating rate): 2°C / min (Frequency): 1Hz (Initial distortion): 0.1% (Relative humidity): 90%

[0119] The adhesion, iodine barrier properties in the adhesive layer, and optical durability of the laminated optical films produced in Examples 1-4 and Comparative Example 1 were evaluated by the methods described below.

[0120] (Adhesion of laminated optical films) The amorphous PET substrate of the laminated optical film manufactured as described above was peeled off, and double-sided tape (No. 500, manufactured by Nitto Denko Corporation) was attached to the peeled surface (iodine-based polarizer surface). Furthermore, adhesive tape (No. 360, manufactured by Nitto Denko Corporation) was attached to the phase difference layer side for reinforcement. Then, the iodine-based polarizer was cut to a size of 200 mm in the direction perpendicular to the stretching direction and 15 mm in the direction parallel to it. After making an incision between the iodine-based polarizer and the phase difference layer with a utility knife, the release film of the double-sided tape was peeled off, and the adhesive side was attached to a glass plate. Next, the thin polarizer and transparent protective film were peeled off at a peeling speed of 20,000 mm / min in the 90-degree direction using an angle-adjustable adhesive / film peeling analyzer (VPA-2, manufactured by Kyowa Interface Chemical Co., Ltd.), and the peeling strength (N / 15 mm) was measured.

[0121] (Iodine barrier properties in the adhesive layer of laminated optical films) To laminate an adhesive layer onto the phase difference layer side of the laminated optical film manufactured as described above, the adhesive layer was manufactured using the following method.

[0122] <Adhesive layer> A monomer mixture containing 99 parts by weight of butyl acrylate (BA) and 1 part by weight of 4-hydroxybutyl acrylate (HBA) was charged into a four-necked flask equipped with a stirring blade, thermometer, nitrogen gas inlet tube, and condenser. Furthermore, 0.1 parts by weight of 2,2'-azobisisobutyronitrile was added to 100 parts by weight of the monomer mixture (solids) as a polymerization initiator along with ethyl acetate. After introducing nitrogen gas and purging the flask with nitrogen while gently stirring, the polymerization reaction was carried out for 7 hours while maintaining the liquid temperature in the flask at around 55°C. Subsequently, ethyl acetate was added to the resulting reaction solution to prepare a solution of (meth)acrylic polymer A1 with a weight-average molecular weight of 1.6 million, with a solids content concentration of 30%. An acrylic adhesive composition was prepared by blending 0.1 parts by weight of an isocyanate crosslinking agent (product name: Takenate D110N, trimethylolpropane xylylene diisocyanate, manufactured by Mitsui Chemicals, Inc.), 0.3 parts by weight of a peroxide crosslinking agent, benzoyl peroxide (product name: Niper BMT, manufactured by Nippon Oil & Fats Co., Ltd.), and 0.08 parts by weight of a silane coupling agent (product name: KBM403, manufactured by Shin-Etsu Chemical Co., Ltd.) with 100 parts by weight of the solid content of the obtained (meth)acrylic polymer A1 solution. The acrylic adhesive composition was uniformly coated onto the surface of a 38 μm thick polyethylene terephthalate film (release liner) treated with a silicone release agent using a fountain coater, and dried in an air-circulating constant temperature oven at 155°C for 2 minutes to form a 20 μm thick adhesive layer on the surface of the release liner.

[0123] The adhesive-coated release liner prepared above was transferred to the phase difference layer side of the laminated optical film, and then the release liner was peeled off. Next, an evaluation sample was prepared by bonding the adhesive layer side of the laminated optical film to an alkali-free glass with a thickness of 0.7 mm and an aluminum vapor-deposited film attached. Using this evaluation sample, a corrosion test was conducted by exposing it to an environment of 60°C and 95% humidity for 240 hours. The presence or absence of corrosion was confirmed visually, and if light leakage occurred in the aluminum vapor-deposited film due to iodine penetrating from the iodine-based polarizer of the laminated optical film, it was determined that corrosion was present.

[0124] (Optical durability of laminated optical films) A polarizing film (sample for humidification durability testing) was prepared by laminating one side of a 0.7 mm thick alkali-free glass via an adhesive layer (20 μm thick). Using this sample, a humidification reliability test of the polarization characteristics was conducted in an environment of 60°C and 95% humidity. Details of the humidification reliability test are shown below. The obtained polarizing film was exposed to an environment of 60°C and 95% humidity for 240 hours, and the degree of polarization before and after exposure was measured using a spectrophotometer with an integrating sphere (V7100, manufactured by JASCO Corporation), and the change in degree of polarization △Pz(%) = |(degree of polarization before exposure (%)) - (degree of polarization after exposure (%))| was calculated.

[0125] [Table 2]

[0126] The results in Table 2 show that the laminated optical films according to Examples 1 to 4 exhibit excellent adhesion between the iodine-based polarizer and the phase difference film, and the barrier function of the adhesive layer against iodine is sufficiently exhibited, thus effectively preventing corrosion of the panel or sensor of the image display device even when used under high temperature and high humidity conditions. On the other hand, although the laminated optical film according to Comparative Example 1 exhibits excellent adhesion between the iodine-based polarizer and the phase difference layer, its barrier function against iodine is inferior, and therefore it cannot prevent corrosion of the panel or sensor of the image display device when used under high temperature and high humidity conditions. Furthermore, the laminated optical film according to Comparative Example 1 also exhibits inferior optical durability. [Explanation of symbols]

[0127] A. Image display device, 1. Iodine-based polarizer, 2. Phase difference film, 3. Adhesive layer, 31. First adhesive layer, 32. Second adhesive layer, 4. Adhesive layer, 5. Third adhesive layer, 6. Transparent protective film, 7. Organic light-emitting diode panel, 10. Laminated optical film

Claims

1. A laminated optical film in which at least an iodine-based polarizer and an optical film are laminated with an adhesive layer in between, The adhesive layer has a two-layer structure consisting of a first adhesive layer on the iodine-based polarizer side and a second adhesive layer on the optical film side. The first adhesive layer is formed of the first cured layer of the first adhesive composition, and logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of the monomer components contained in the first adhesive composition, is 2.5 or higher. The laminated optical film is characterized in that the second adhesive layer is formed from a second cured layer of the second adhesive composition, and logPow, which represents the octanol / water partition coefficient based on the weighted average of the mole fractions of monomer components contained in the second adhesive composition, is less than 2.

5.

2. The first cured layer has a moisture permeability of 150 g / m². ２ - The laminated optical film according to claim 1, wherein the aging period is 24 hours or less.

3. The laminated optical film according to claim 1, wherein the optical film is a liquid crystal phase difference film.

4. The laminated optical film according to claim 3, wherein the thickness of the phase difference film is 5 μm or less.

5. The laminated optical film according to claim 1, wherein the thickness of the first adhesive layer is 3 μm or less.

6. The laminated optical film according to claim 1, wherein the thickness of the second adhesive layer is 3 μm or less.

7. The laminated optical film according to claim 1, wherein the thickness of the iodine-based polarizer is 8 μm or less.

8. The laminated optical film according to claim 1, wherein the first adhesive composition contains at least a (meth)acrylate compound and a photopolymerization initiator, and the (meth)acrylate compound contains (meth)acrylate (A) having a cyclic hydrocarbon skeleton in its molecule.

9. The laminated optical film according to claim 1, wherein the first adhesive composition contains 70 parts by mass or more of the (meth)acrylate (A) when the total amount of the (meth)acrylate compound is 100 parts by mass.

10. The laminated optical film according to claim 8, wherein the (meth)acrylate (A) is a compound having 5 to 12 carbon atoms that constitute a cyclic hydrocarbon skeleton within the molecule.

11. The laminated optical film according to claim 8, wherein the (meth)acrylate (A) is at least a bifunctional (meth)acrylate.

12. The (meth)acrylate (A) is represented by the following formulas (A1) to (A4); 【Chemistry 1】 The laminated optical film according to claim 8, wherein the compound is at least one compound selected from the group consisting of the compounds described above.

13. The laminated optical film according to claim 8, wherein the first adhesive composition further contains a (meth)acrylate (B) containing a hydroxyl group.

14. The laminated optical film according to claim 8, wherein the content of (meth)acrylate (A) relative to (meth)acrylate (B) is in the range of 2 to 6 times.

15. The laminated optical film according to claim 8, wherein the adhesive composition contains 5 to 25 parts by mass of the (meth)acrylate (B) when the total amount of the (meth)acrylate compound is 100 parts by mass.

16. An image display device comprising the laminated optical film described in claim 1.

17. An organic EL display device comprising the laminated optical film described in claim 1.

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