Patent Application
20190106599
The present invention relates to an active-energy-ray-curable adhesive composition through which, for example, a polarizing film, and an optical film other than polarizers are adhered to each other; a laminated polarizing film yielded using this composition; and a method for producing the laminated polarizing film. This laminated film is used singly or in the form of a laminated optical film in which an optical film is further laminated on the laminated polarizing film to make it possible to form an image display device, such as a liquid crystal display device (LCD), an organic EL display device, and CRT or a PDP.
About any liquid crystal display device or the like, in the light of the image forming manner thereof, it is indispensable to arrange polarizers, respectively, onto both sides of a liquid crystal cell. In general, polarizing films are bonded thereonto. In order to improve a liquid crystal panel in display quality of its display, besides a polarizing film, various optical films are used. The used optical films are, for example, a retardation film for preventing the display from being colored, a viewing angle enlargement film for improving the liquid crystal display in viewing angle, and a brightness enhancement film for enhancing the display in contrast.
In the case of combining a polarizing film as described above and an optical film (for example, a retardation film) with each other to be used as a laminated polarizing film, the polarizing film and the optical film are usually laminated onto each other through a pressure-sensitive-adhesive layer (for example, Patent Document 1). Patent Document 1 suggests, as the pressure-sensitive-adhesive layer, a layer having a storage modulus of 0.3 MPa or more at 23° C. from the viewpoint of a prevention of light-leakage from the laminated polarizing film, and others. Moreover, Patent Document 1 makes use of a pressure-sensitive-adhesive layer having a thickness of 5 to 100 μm to cause the pressure-sensitive-adhesive layer to satisfy peel strength.
Patent Document 2 listed below describes a laminated polarizing film in which a polarizing film is laminated onto an optical film other than polarizers, and describes a technique therefor that an adhesive layer for the lamination is a low-elastic-modulus adhesive layer having a storage modulus of 3.0×105 to 1.0×108 Pa at 25° C., and the adhesive layer is designed to have a thickness of 0.1 to 5 μm.
About the above-mentioned laminated polarizing films, in a retardation film used in each of these films, molecules are face aligned; thus, when the retardation film is dropped, or receives any other impact, this retardation film is easily cleaved. Accordingly, for example, a laminated product of a polarizing film and the retardation film is insufficient in impact resistance.
The laminated polarizing films are each bonded onto a liquid crystal cell to be made into a panel state, and then supplied to, for example, a heating test or a freezing cycle test (heat shock cycle test). However, it is difficult that the pressure-sensitive-adhesive layer described in Patent Document 1 follows a dimension change of the polarizing film that is generated by the test. When the tested laminated polarizing film is made into a crossed Nichol state to be observed, display defects such as streak unevenness are observed. Thus, about laminated optical films, it is desired that streak unevenness and other defects are not generated in the state that their laminated polarizing film is made into a crossed Nichol state even after the above-mentioned test (hereinafter, this property will be referred to as “heating buckling resistance”).
According to the technique described in Patent Document 2, the following has been made evident: in spite of a combination of two or more out of various films included in the laminated polarizing film, the laminated polarizing film becomes instable in adhering strength; alternatively, a period is required from a time when an adhesive is painted onto any one of the films to a time when the adhesive expresses adhering strength; and such causes result in problems about the adhering strength between the films, and the productivity of laminated polarizing films.
Apart from the above, in recent years, for organic polymeric materials, conflicting properties are frequently required. In the actual situation, a single organic polymeric material does not easily satisfy the required properties. In order to cause a product to satisfy conflicting properties, suggested is a technique of adding, to an organic polymeric material, a different-species material different in nature therefrom to complex these materials with each other in many fields. In the adhering technique, it is conceivable that when two different-specie adherends are bonded to each other, an adhesive layer is made into a bi-layered structure to heighten the adherends in adhesion therebetween. However, when the adhesive layer is made into the bi-layered structure, stress is concentrated to the interface therebetween so that the adhering strength of the adhesive layer may be unfavorably lowered.
In the case of selecting, as one of the adherends, for example, a retardation film as described above, an adhesive-agent-blending design for giving affinity to a molecular-aligned surface of the retardation film is entirely different from an adhesive-agent-blending design for giving a low elasticity thereto to improve the whole in impact resistance. Thus, in order to cause an adhesive layer obtained by curing an adhesive composition to express two or more conflicting properties, it is necessary to create an unprecedentedly blending idea newly.
An object of the present invention is to provide an active-energy-ray-curable adhesive composition that is usable for a laminated polarizing film in which a polarizing film is laminated on/over an optical film other than polarizing films, and for other articles, and that can form an adhesive layer improved in adhesion or adhering performance, impact resistance, and heating buckling resistance with a good balance. Another object of the invention is to provide a laminated polarizing film that includes a polarizing film, and an optical film which is a film other than polarizing films and which is laminated on/over the polarizing film, and that is good in impact resistance and heating buckling resistance; and a method for producing a laminated polarizing film that can shorten a period from a time when an adhesive is painted to a time when the adhesive is cured, so as to be excellent in producing performance.
Still another object of the present invention is to provide a laminated optical film using the above-mentioned laminated polarizing film, and an image display device using the laminated polarizing film or the laminated optical film.
In order to solve the above-mentioned problems, the inventors have made eager investigations to find out that the problems can be solved by a polarizing film and others that are described below. Thus, the present invention has been accomplished.
The present invention relates to an active-energy-ray-curable adhesive composition, including at least radical polymerizable compounds, in which the radical polymerizable compounds include a component A having a log Pow of −2 to 2, and a component B having a log Pow more than 7, each of these log Pow values representing an octanol/water distribution coefficient.
In the active-energy-ray-curable adhesive composition, it is preferred that the component A includes at least one nitrogen-containing monomer selected from the group consisting of (meth)acrylamide derivatives, amino-group-containing monomers, and nitrogen-containing and heterocycle-containing vinyl monomers.
In the active-energy-ray-curable adhesive composition, it is preferred that the component B includes an alkyl (meth)acrylate having 18 to 20 carbon atoms.
In the active-energy-ray-curable adhesive composition, it is preferred that when a total amount of the radical polymerizable compounds is regarded as 100% by weight, a proportion of the component A is 10% or more by weight.
In the active-energy-ray-curable adhesive composition, it is preferred that when the total amount of the radical polymerizable compounds is regarded as 100% by weight, a proportion of the component B is 15% or more by weight.
The active-energy-ray-curable adhesive composition preferably further includes a polyfunctional radical polymerizable compound having a log Pow that is more than 2, and is 7 or less.
In the active-energy-ray-curable adhesive composition, it is preferred that the polyfunctional radical polymerizable compound is an alkylene di(meth)acrylate having 7 to 12 carbon atoms.
The active-energy-ray-curable adhesive composition preferably further includes not only the radical polymerizable compounds but also an acrylic oligomer obtained by polymerizing a (meth)acrylic monomer.
The active-energy-ray-curable adhesive composition preferably includes a radical polymerizable compound having a hydroxyl group.
The active-energy-ray-curable adhesive composition preferably further includes not only the radical polymerizable compounds but also a silane coupling agent.
In the active-energy-ray-curable adhesive composition, it is preferred that the silane coupling agent is a silane coupling agent having no radical polymerizable functional group.
The active-energy-ray-curable adhesive composition preferably includes a radical polymerizable compound having an active methylene group, and a radical polymerization initiator having hydrogen-withdrawing effect.
In the active-energy-ray-curable adhesive composition, it is preferred that the active methylene group is an acetoacethyl group.
In the active-energy-ray-curable adhesive composition, it is preferred that the radical polymerizable compound having the active methylene group is acetoacethoxyalkyl (meth)acrylate.
In the active-energy-ray-curable adhesive composition, it is preferred that the radical polymerization initiator is a thioxanthone-based radical polymerization initiator.
The present invention also relates to a laminated polarizing film, including a polarizing film, and an optical film or optical films which are other than polarizers and which are laminated on/over the polarizing film to interpose an adhesive layer (a) between the polarizing film and the optical film, or to interpose adhesive layers (a), respectively, between the polarizing film and the optical films, in which the polarizing film is a film in which a transparent protective film is laminated on/over one surface of a polarizer to interpose an adhesive layer (b) between the one surface and the transparent protective film, or transparent protective films are laminated, respectively, on/over both surfaces of a polarizer to interpose adhesive layers (b), respectively, between both the surfaces and the transparent protective films, and further the adhesive layer(s) (a) is/are laminated on/over the transparent protective film or the respective transparent protective films; and the adhesive layer(s) (a) is/are (each) formed in the form of a cured product layer yielded by radiating an active energy ray to the active-energy-ray-curable adhesive composition descried in any one of the above-mentioned paragraphs concerned.
In the laminated polarizing film, it is preferred that the optical film(s) is/are (each) a retardation film.
In the laminated polarizing film, it is preferred that the adhesive layer(s) (a) has/have a glass transition temperature of 40° C. or lower.
In the laminated polarizing film, it is preferred that the polarizing film is a film in which the transparent protective films are laminated, respectively, on/over both the surfaces of the polarizer to interpose an adhesive layer (a) and the adhesive layer (b), respectively, between both the surfaces of the polarizer, and the polarizing film.
In the laminated polarizing film, it is preferred that the adhesive layer(s) (b) has/have a glass transition temperature higher than 40° C.
In the laminated polarizing film, it is preferred that the adhesive layer(s) (b) is/are (each) an adhesive layer (b1) having a storage modulus of 1.0×106 to 1.0×1010 Pa at 85° C., and satisfying a thickness of 0.03 to 3 μm.
In the laminated polarizing film, it is preferred that the polarizing film is a film in which the transparent protective films are laid, respectively, on/over both the surfaces of the polarizer to interpose the adhesive layers (b), respectively, between both the surfaces of the polarizer and the transparent protective films, and the adhesive layers (b) are each an adhesive layer (b1) having a storage modulus of 1.0×106 to 1.0×1010 Pa at 85° C. and satisfying a thickness of 0.03 to 3 μm.
In the laminated polarizing film, it is preferred that the polarizing film is a film in which the transparent protective films are laid, respectively, on/over both the surfaces of the polarizer to interpose the adhesive layers (b), respectively, between both the surfaces of the polarizer and the transparent protective films, and the adhesive layer (b) on/over one of the surfaces of the polarizer is an adhesive layer (b1) having a storage modulus of 1.0×106 to 1.0×1010 Pa at 85° C. and satisfying a thickness of 0.03 to 3 μm, and the adhesive layer (b) on/over the other surface of the polarizer is an adhesive layer (b2) having a storage modulus of 1.0×104 to 1.0×108 Pa at 85° C. and satisfying a thickness of 0.1 to 25 μm.
In the laminated polarizing film, it is preferred that the polarizer has a thickness of 1 to 10 μm.
In the laminated polarizing film, it is preferred that about the transparent protective film(s), the transparent protective film on/over at least the one surface of the polarizer is a retardation film.
In the laminated polarizing film, it is preferred that about the transparent protective film(s), the transparent protective film on/over at least the one surface of the polarizer has a log Pow of −2 to 2, the log Pow representing an octanol/water distribution coefficient.
In the laminated polarizing film, it is preferred that the transparent protective film(s) is/are (each) a reverse wavelength dispersion type retardation film satisfying the following expressions (1) to (3):
0.70<Re[450]/Re[550]<0.97 (1),
1.5×10−3<Δn<6×10−3 (2), and
1.13<NZ<1.50 (3)
in which Re[450] and Re[550] are, respectively, an in-plane retardation value of the retardation film that is measured at a wavelength of 450 nm at 23° C., and an in-plane retardation value of the retardation film that is measured at a wavelength of 550 nm at 23° C.; Δn is an in-plane birefringence “nx−ny” of the retardation film when the retardation film has a refractive index nx in a slow axis direction of the film, and has a refractive index ny in a fast axis direction of the film; and when the retardation film has a refractive index nz in a thickness direction of the film, NZ is a ratio between “nx−nz”, which is a birefringence of the film in the thickness direction, and “nx−ny”, which is an in-plane birefringence of the film.
In the laminated polarizing film, it is preferred that about the optical film(s), the transparent protective film on/over at least the one surface of the polarizer has a log Pow of −2 to 2, the log Pow representing an octanol/water distribution coefficient.
In the laminated polarizing film, it is preferred that the optical film(s) is/are (each) a reverse wavelength dispersion type retardation film satisfying the following expressions (1) to (3):
0.70<Re[450]/Re[550]<0.97 (1),
1.5×10−3<Δn<6×10−3 (2), and
1.13<NZ<1.50 (3)
in which Re[450] and Re[550] are, respectively, an in-plane retardation value of the retardation film that is measured at a wavelength of 450 nm at 23° C., and an in-plane retardation value of the retardation film that is measured at a wavelength of 550 nm at 23° C.; Δn is an in-plane birefringence “nx−ny” of the retardation film when the retardation film has a refractive index nx in a slow axis direction of the film, and has a refractive index ny in a fast axis direction of the film; and when the retardation film has a refractive index nz in a thickness direction of the film, NZ is a ratio between “nx−nz”, which is a birefringence of the film in the thickness direction, and “nx−ny”, which is an in-plane birefringence of the film.
In the laminated polarizing film, it is preferred that when the polarizing film, and the optical film or each of the optical films are forcibly peeled off from each other, the adhesive layers (a) or each of the optical films (a) is cohesively fractured.
The laminated polarizing film preferably shows an interlayer adhering strength of 0.9 N/15-mm or more when the polarizing film, and the optical film or each of the optical films are forcibly peeled off from each other.
The present invention also relates to a method for producing the laminated polarizing film described in any one of the paragraphs concerned, including: a painting step of painting an active-energy-ray-curable adhesive composition for forming the adhesive layer (a) to at least one surface of the transparent protective film on a side of the polarizing film on which the adhesive layer (a) is laminated, and the optical film; a bonding step of causing the polarizing film and the optical film to bond each other; and an adhering step of radiating the active energy ray to the resultant workpiece to cure the active-energy-ray-curable adhesive composition to cause the polarizing film and the optical film to adhere onto each other through the resultant adhesive layer (a). In the method for producing the polarizing film, it is preferred that the active energy ray shows a ratio of 100:0 to 100:50, this ratio being a ratio between an integrated illuminance of rays in a wavelength range from 380 to 440 nm and an integrated illuminance of rays in a wavelength range from 250 to 370 nm.
The present invention also relates to a laminated optical film in which at least one laminated polarizing film as described in any one of the paragraphs concerned is laminated; or an image display device in which a laminated polarizing film as described in any one of the paragraphs concerned, or a laminated optical film as described in the paragraph concerned is used.
In order to bond adherends of two different species to each other, the formation of an adhesive layer into a bi-layered structure is favorable from the viewpoint of an improvement of the two adherends in adhering strength therebetween. As described above, however, it is feared that the adhering strength is reversely lowered by, for example, an interfacial peel inside the adhesive layer. The active-energy-ray-curable adhesive composition of the present invention includes at least radical polymerizable compounds, and the radical polymerizable compounds include a component A having a log Pow of −2 to 2 and a component B having a log Pow more than 7, these log Pows being each an octanol/water distribution coefficient. In other words, the active-energy-ray-curable adhesive composition according to the invention includes the component A and the component B, which are appropriately different from each other in log Pow. This matter makes an adhesive layer made of the composition into an inclined structure in which the concentration proportion of the component A (or that of the component B) is leaned toward one side in the thickness direction of the adhesive layer. This manner allows to form the adhesive layer to show two or more excellent properties.
When the adhesive layer is, for example, a layer for adhering a retardation film as an adherend to another adherend, the component A, which shows affinity with this film, is unevenly distributed in the retardation film side of the resultant laminate to form an evenly distributed layer (anchor layer) between the adhesive layer and the retardation film. The formation allows to cause the adhesive layer to express an intensely adhering strength rapidly to the retardation film to improve adhesion between the adhesive layer and the retardation film. The unevenly distribution of the component A toward the retardation film side (the formation of the anchor layer) is realized by the presence of the component B, which can form the inclined structure by an appropriate phase-separation of the components A and B from each other. In the meantime, the component B itself is unevenly distributed in a large proportion on the side of the laminate that is opposite to the retardation film. Thus, this matter contributes greatly to special advantageous effects originating from the component B, for example, improvements of the adhesive layer in adhesion water resistance, and of the laminated polarizing film in impact resistance and heating buckling resistance.
The laminated polarizing film of the present invention is in particular favorable in heating buckling resistance and impact resistance when the polarizer included in the polarizing film has a thickness of 1 to 10 μm to be a thin polarizer. The thin polarizer is small in the above-mentioned dimension change, so that the polarizer undergoes a dimension change relative to the dimension change of the transparent protective film, or any optical film other than polarizers. Consequently, the thin polarizer tends to show a poorer heating buckling resistance than polarizers each having a thickness of 10 μm or more. Moreover, the thin polarizer has a higher elastic modulus than the polarizers, the thickness of which is 10 μm or more, to tend to be poorer in impact absorption than the polarizers, the thickness of which is 10 μm or more. The laminated polarizing film of the invention has the adhesive layer, which has the component-inclined structure as described above, so that the laminated polarizing film can satisfy heating buckling resistance and impact resistance even when a thin polarizer is used.
The active-energy-ray-curable adhesive composition according to the present invention is made to have, in particular, a blend design as follows: a component high in affinity with an adherend, out of the components A and B, is rapidly distributed unevenly toward the adherend to form an unevenly distributed layer. Thus, in the method for producing a laminated polarizing film using this composition, the composition expresses a high adhesion even in the case of shortening a period from a time when the composition is painted to a time when an active-energy-ray-curable adhesive composition is radiated thereto. For this reason, the method according to the invention for producing a laminated polarizing film is excellent in performance of producing laminated polarizing films.
The active-energy-ray-curable adhesive composition of the present invention is usable when an adhesive layer is formed to laminate two or more films onto each other. The composition is in particular preferably usable for a laminated polarizing film in which a polarizing film and an optical film are laminated to each other. A description will be made hereinafter about embodiments of a laminated polarizing film as an example with reference to the drawings.
The adhesive layer (a) or each of the adhesive layers (a) preferably has a glass transition temperature of 40° C. or lower. When the glass transition temperature is 40° C. or lower, a laminated polarizing film good in impact resistance can be yielded. The glass transition temperature of the adhesive layer (a) is preferably 35° C. or lower, more preferably 30° C. or lower. The thickness of the adhesive layer (a) is preferably from 0.1 to 5 μm.
In each of the polarizing films (P), the thickness of the adhesive layer (b) or each of the adhesive layers (b) for laminating the polarizer (1) to the (corresponding) transparent protective film (2) is usually from 0.1 to 25 μm from the viewpoint of the adhesion thereof.
The polarizing film (P1) in the laminated polarizing film in
At 25° C., the storage modulus of the adhesive layer (b1) is preferably from 5.0×107 to 1.0×1010 Pa, or 1.0×108 to 7.0×109 Pa, more preferably from 5.0×108 to 5.0×109 Pa.
The respective polarizing films (P2) and (P3) in the laminated polarizing films in
In the same manner as the adhesive layer (b1) in
The adhesive layer (b2) in each of
At 25° C., the storage modulus of the adhesive layer (b2) is preferably from 1.0×104 to 1.0×108 Pa, or 5.0×104 to 7.0×107 Pa, more preferably from 1.0×105 to 1.0×107 Pa.
When the storage modulus and the thickness of each of the adhesive layers (b1) and (b2) are controlled into these ranges, respectively, the polarizer can be favorably restrained from being cracked when the laminated polarizing film is subjected to a heat shock cycle test, and each of the laminated polarizing films is favorably more satisfactory in impact resistance.
In the polarizing film (P) in the laminated polarizing film in
About each of the embodiments illustrated in
In the embodiment illustrated in
The adhesive layer (b) is preferably an adhesive layer having a glass transition temperature higher than 40° C. The polarizer (1) and one of the transparent protective films (2) are strongly bonded to each other through the adhesive layer (b). Thus, the laminated polarizing film is good in endurance, and can be prevented from undergoing “heat shock cracking”. The “heat shock cracking” means a phenomenon that, for example, when the polarizer is expanded and contracted, the polarizer is cracked in the stretched direction thereof. In order to prevent this phenomenon, it is important to restrain the polarizer from being expanded and contracted in a heat shock temperature range (of −40 to 60° C.). The adhesive layer (b) can be restrained from being abruptly changed in elastic modulus in the heat shock temperature range to decrease expanding- and contracting-forces acting to the polarizer. Thus, this layer can prevent the generation of heat shock cracking. About the adhesive layer (b), the glass transition temperature thereof is selected to be preferably a temperature higher than 40° C., more preferably 60° C. or higher, even more preferably 70° C. or higher, even more preferably 80° C. or higher. In the meantime, if the adhesive layer (b) of the glass transition temperature of the adhesive layer (b) is too high, the polarizing plate is lowered in flexibility. Thus, the glass transition temperature of the adhesive layer (b) is preferably 300° C. or lower, more preferably 240° C. or lower, even more preferably 180° C. or lower.
In the embodiment illustrated in
The above-mentioned adhesive layer (a) or each of the above-mentioned adhesive layers (a) may be in a cured product layer of the active-energy-ray-curable adhesive composition according to the present invention. Hereinafter, the active-energy-ray-curable adhesive composition according to the invention will be described.
For the active-energy-ray-curable adhesive composition according to the present invention, an electron curable, or ultraviolet curable adhesive may be used. Ultraviolet curable adhesives can be roughly classified into radical polymerization curable adhesives and cationic polymerization curable adhesives
A curable component of each of the radical polymerization curable adhesives may be a compound having a (meth)acryloyl group or a radical polymerizable compound having a vinyl group. The curable component may be a monofunctional component or a bi- or higher polyfunctional component. Such curable components may be used singly or in any combination of two or more thereof. The curable component is preferably, for example, a compound having a (meth)acryloyl group.
A curable component of each of the cationic polymerization curable adhesives may be a compound having an epoxy group, oxetanyl group or vinyl group. The compound having an epoxy group is not particularly limited as far as the compound is a compound having in the molecule thereof at least one epoxy group, and the compound may be a generally known curable epoxy compound that may be of various types. A preferred example of the epoxy compound is a compound having in the molecule thereof at least two epoxy groups and at least one aromatic ring (hereinafter referred to as an “aromatic epoxy compound”); or a compound having at least two epoxy groups in which at least one of these groups is formed between adjacent two carbon atoms included in an alicyclic ring.
As the active-energy-ray-curable adhesive, a liquid substance is used which does not substantially contain any organic solvent and further has a viscosity of 1 to 100 cp/25° C. The use of this liquid substance allows to form a thin adhesive layer (a) having a thickness of 0.1 to 5 μm. The point that the adhesive of the liquid substance is used to form the adhesive layer (a) is different from the point that a pressure-sensitive-adhesive layer used to form a pressure-sensitive-adhesive layer does not show any liquid substance form. Also from this point, a difference is evident between the adhesive layer and the pressure-sensitive-adhesive layer. The above-mentioned viscosity is preferably from 5 to 100 cp/25° C., more preferably from 10 to 70 cp/25° C. The wording “does not substantially contain any organic solvent” means that the active-energy-ray-curable adhesive may contain an organic solvent in a proportion of 10% or less by weight of the whole of the active-energy-ray-curable adhesive. The content of the organic solvent is preferably 5% or less by weight, more preferably 3% or less by weight. The organic solvent is a liquid having a flashing point of 40° C. or lower. The active-energy-ray-curable adhesive may not contain any organic solvent.
The active-energy-ray-curable adhesive composition according to the present invention includes a component A having a log Pow of −2 to 2.
The octanol/water distribution coefficient (log Pow) is an index representing the lipophilicity of a substance, and denotes the logarithmic value of the octanol/water distribution coefficient of the substance. The matter that the log Pow of a substance is high means that the substance is lipophilic, that is, that the substance is low in water absorption coefficient. Although the log Pow value is measurable (by a flask shaking method described in JIS-Z-7260), the value can be calculated through calculation. In this description, log Pow values calculated according to a software Chem Draw Ultra manufactured by CambridgeSoft Corp. are used.
The component A having a log Pow of −2 to 2 may be any compound having a log Pow of −2 to 2 out of radical polymerizable compounds. The component A is in particular preferably such a compound that has a polar group. Examples thereof preferably include at least one nitrogen-containing monomer selected from the group consisting of (meth)acrylamide derivatives, amino-group-containing monomers, and nitrogen-containing and heterocycle-containing vinyl monomers. The (meth)acrylamide derivatives are more preferred. Specific examples thereof include hydroxyethylacrylamide (Log Pow: −0.56), N-methylolacrylamide (Log Pow: −0.94) and other hydroxyl-group-containing alkylacrylamides, acryloylmorpholine (Log Pow: −0.2) and other cyclic amide compounds, N-methoxymethylacrylamide (Log Pow: 0.08) and other alkoxyalkylacrylamides, N-vinyl-2-pyrrolidone (Log Pow: −0.24) and other heterocyclcyle-containing compounds, dimethylaminoethylacrylamide (Log Pow: −0.04) and other amino-group-containing monomers, dimethylaminoethyl acrylate (Log Pow: 0.64) and other nitrogen-containing and acryloyl-group-containing monomers, diethylacrylamide (Log Pow: 1.69), dimethylacrylamide (Log Pow: −0.58) and other dialkyl(meth)acrylamides, N-vinylformamide (trade name: “BEAM SET 770”, manufactured by Arakawa Chemical Industries, Ltd.; Log Pow: −0.25), γ-butyrolactone acrylate (trade name: “GBLA”, manufactured by Osaka Organic Chemical Industry Ltd.; Log Pow: 0.19), acrylic acid (Log Pow: 0.69), acrylic acid dimer(trade name: “β-CEA”, Daicel Corp.; Log Pow: 0.2), 2-hydroxyethyl acrylate (trade name: “HEA”, manufactured by Osaka Organic Chemical Industry Ltd.; Log Pow: 0.28), 4-hydroxybutyl acrylate (trade name: “4-HBA”, manufactured by Osaka Organic Chemical Industry Ltd.; Log Pow: 0.68), glycidyl methacrylate (trade name: “LIGHT ESTER G”, manufactured by Kyoeisha Chemical Co., Ltd.; Log Pow: 0.57), and acrylic acid multimer ester of tetrahydrofurfuryl alcohol (trade name: “VISCOAT #150D”, manufactured by Osaka Organic Chemical Industry Ltd.; Log Pow: 0.60). Out of these examples, preferred are acryloyl morpholine, N-vinyl-2-pyrrolidone, diethylacrylamide, and dimethylacrylamide.
If the log Pow value of the component A is smaller than −2, the component A does easily coexist with the component B so that the phase-separation of the two completely advances. Consequently, the adhesive composition liquid becomes poor in stability. If the log Pow value of the component A is larger than 2, the affinity of the component A with the component B is unfavorably generated so that the component A is not easily distributed unevenly toward the film interface. Thus, the resultant adhesive layer is unfavorably lowered in adhesion.
The log Pow value of the component A is preferably from −1.5 to 1.5, more preferably from −1.0 to 1.0.
The proportion of the monomer A is preferably 10% or more, more preferably 15% or more, even more preferably 20% or more by weight of the whole of the radical polymerizable compounds, the proportion thereof being 100% by weight. When the proportion is set to 10% or more by weight, an initiative generation of an uneven distribution of the component A toward the film interface is favorably caused.
<Component B Having Log Pow More than 7>
The active-energy-ray-curable adhesive composition according to the present invention includes a component B having a log Pow more than 7 in addition to the component A, the log Pow of which is from −2 to 2.
The component B is preferably an alkyl (meth)acrylate having 18 or more carbon atoms. Examples of the alkyl group include stearyl, isostearyl, nonadecyl, isonanodecyl, icosyl, and isoicosyl groups. Specific examples of the component B include isostearyl acrylate (trade name: ISTA, manufactured by Osaka Organic Chemical Co.; Log Pow 7.5), and isostearyl methacrylate (Log Pow: 7.81), and other alkyl (meth)acrylate monomers. Out of such components, branched long-chain alkyl (meth)acrylate monomers are preferred since these monomers do not make the adhesive layer layer(s) (a) excessively high in glass transition temperature. Specifically, isostearyl acrylate is preferred.
If the log Pow value of the component B is smaller than 7, the affinity of the component B with the component A is unfavorably generated so that an uneven distribution of the component A is not easily caused toward the film interface. Consequently, the resultant adhesive layer is unfavorably lowered in adhesion.
The proportion of the monomer B is preferably 15% or more, more preferably 25% or more, even more preferably 35% or more by weight of the whole of the radical polymerizable compounds, the proportion thereof being 100% by weight. When the proportion is set to 15% or more by weight, an initiative generation of an uneven distribution of the component A toward the film interface is favorably caused.
Furthermore, the present invention may include a radical polymerizable compound having a log Pow value of 2 to 7. Specific examples thereof include dicyclopentenyl acrylate (trade name: “FANCRYL FA-511AS”; Log Pow: 2.26), butyl acrylate (trade name: “BUTYL ACRYLATE”, manufactured by Mitsubishi Chemical Corp.; Log Pow: 2.35), dicyclopentanyl acrylate (trade name: “FANCRYL FA-513AS”, manufactured by Hitachi Chemical Co., Ltd.), isobornyl acrylate (trade name: “LIGHT ACRYLATE IB-XA”, manufactured by Kyoeisha Chemical Co., Ltd.; Log Pow: 3.27), a neopentyl glycol acrylic acid adduct of hydroxypivalic acid (trade name: “LIGHT ACRYLATE HPP-A”, manufactured by Kyoeisha Chemical Co., Ltd.; Log Pow: 3.35), and o-phenylphenol EO-modified acrylate (trade name: “FANCRYL FA-301A”, manufactured by Hitachi Chemical Co., Ltd.; Log Pow: 3.98). It is preferred to use, out of these compounds, butyl acrylate in the present invention.
For an improvement of the adhesive layer in adhering strength and water resistance, the proportion of the component, the log Pow of which is from 2 to 7, is preferably from 2 to 60%, more preferably from 3 to 40% by weight of the whole of the radical polymerizable compounds, the proportion thereof being 100% by weight.
The polyfunctional radical polymerizable compound is a compound having at least two radical polymerizable functional groups each having an unsaturated double bond, such as a (meth)acryloyl group or a vinyl group. Examples of the polyfunctional radical polymerizable compound include tetraethylene glycol diacrylate (Tg of a homopolymer thereof, which will be referred to only as Tg hereinafter: 50° C.), polyethylene glycol diacrylate, polypropylene glycol diacrylates (n=3, Tg: 69° C.), (n=7, Tg: −8° C.) and (n=12, Tg: −32° C.) and other polyalkylene glycol diacrylates, neopentyl glycol diacrylate (Tg: 117° C.), 3-methyl-1,5-pentanediol diacrylate (Tg: 105° C.), 1,6-hexanediol diacrylate (Tg: 63° C.), 1,9-nonanediol diacrylate (Tg: 68° C.), a mixture (Tg: 88° C.) of 2-methyl-1,8-octanediol diacrylate and 1,9-nonanediol diacrylate, dimethylol-tricyclodecane diacrylate (Tg: 75° C.), an EO adduct diacrylate of bisphenol A (Tg: 75° C.), bisphenol F EO-modified (n=2) diacrylate (Tg: 75° C.), bisphenol A EO-modified (n=2) diacrylate (Tg: 75° C.), isocyanuric acid EO-modified diacrylate (Tg: 166° C.), trimethylolpropane triacrylate (Tg: 250° C. or higher), trimethylolpropane PO-modified triacrylates (n=1, Tg: 120° C.) and (n=2, Tg: 50° C.), trimethylolpropane EO-modified triacrylates (n=1, Tg: unmeasured) and (n=2, Tg: 53° C.), isocyanuric acid EO-modified di- and tri-acrylates (di: 30 to 40%, Tg: 250° C. or higher), and (di: 3 to 13%, Tg: 250° C. or higher), pentaerythritol tri- and tetra-acrylates (tri: 65 to 70%, Tg: 250° C. or higher), (tri: 55 to 63%, Tg: 250° C. or higher), (tri: 40 to 60%, Tg: 250° C. or higher), (tri: 25 to 40%, Tg: 250° C. or higher) and (tri: less than 10%, Tg: 250° C. or higher), ditrimethylolpropane tetraacrylate (Tg: 250° C. or higher), dipentaerythritol penta- and hexa-acrylates (penta: 50 to 60%, Tg: 250° C. or higher), (penta: 40 to 50%, Tg: 250° C. or higher), (penta: 30 to 40%, Tg: 250° C. or higher), (penta: 25 to 35%, Tg: 250° C. or higher) and (penta: 10 to 20%, Tg: 250° C. or higher), and respective (meth)acrylates corresponding to these compounds. Other examples of the polyfunctional radical polymerizable compound include oligomer (meth)acrylates such as various polyurethane (meth)acrylates, polyester (meth)acrylates, and polyepoxy (meth)acrylates. The polyfunctional radical polymerizable compound (A) is also preferably a commercially available product. Examples thereof include products LIGHT ACRYLATE 4EG-A, LIGHT ACRYLATE 9EG-A, LIGHT ACRYLATE NP-A, LIGHT ACRYLATE MPD-A, LIGHT ACRYLATE 1.6HX-A, LIGHT ACRYLATE 1.9ND-A, LIGHT ACRYLATE MOD-A, LIGHT ACRYLATE DCP-A, and LIGHT ACRYLATE BP-4EAL (each manufactured by Kyoeisha Chemical Co., Ltd.), ARONIXs M-208, M-211B, M-215, M-220, M-225, M-270, M-240, M-309, M-310, M-321, M-350, M-360, M-313, M-315, M-306, M-305, M-303, M-452, M-450, M-408, M-403, M-400, M-402, M-404, M-406, M-405, M-1100, M-1200, M-6100, M-6200, M-6250, M-6500, M-7100, M-7300, M-8030, M-8060, M-8100, M-8530, M-8560, and M-9050 (each manufactured by Toagosei Co., Ltd.), and SR-531 (manufactured by SARTOMER Inc.) and CD-536 (manufactured by SARTOMER Inc.). The polyfunctional radical polymerizable compound (A) is preferably a homopolymer having a Tg of −40 to 100° C.
The proportion of the polyfunctional radical polymerizable compound is preferably from 1 to 65% by weight of the whole of the radical polymerizable compounds in the active-energy-ray-curable adhesive, the proportion of the whole being 100% by weight. When the proportion is set to 1% or more by weight, the adhesive layer (a) favorably satisfies impact resistance, heating buckling resistance, adhesion endurance, and polarizer cracking resistance.
In the case of using, out of the above-mentioned polyfunctional radical polymerizable compounds, a polyfunctional radical polymerizable compound having a log Pow of more than 2 and 7 or less, the phase-separation of the components A and B from each other is restrained to improve the adhesive composition favorably in liquid stability. The polyfunctional radical polymerizable compound having a log Pow of more than 2, and 7 or less may be any compound having a log Pow of more than 2, and 7 or less out of the above-mentioned polyfunctional radical polymerizable compounds, and is preferably an alkylene di(meth)acrylate having 7 to 12 carbon atoms. A specific example thereof is 1,9-nonanediol diacrylate (trade name: “LIGHT ACRYLATE 1,9ND-A”, manufactured by Kyoeisha Chemical Co., Ltd.; log Pow: 3.68). The proportion of the polyfunctional radical polymerizable compound having a log Pow of more than 2, and 7 or less is preferably from 2 to 35%, more preferably from 4 to 25%, even more preferably from 6 to 15% by weight of the whole of the radical polymerizable compounds, the proportion thereof being 100% by weight.
The active-energy-ray-curable adhesive composition according to the present invention may contains, as a radical polymerizable compound that is a monofunctional radical polymerizable compound, an alkyl (meth)acrylate having an alkyl group having 2 to 13 carbon atoms. The alkyl (meth)acrylate is, for example, a (meth)acrylate having a linear or branched alkyl group having 1 to 13 carbon atoms. Examples of the alkyl group include methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, amyl, hexyl, cyclohexyl, heptyl, 2-ethylhexyl, isooctyl, nonyl, decyl, and isodecyl groups. These groups may be used singly or in combination. The alkyl (meth)acrylate is preferably an alkyl (meth)acrylate in which the alkyl group has 3 to 13 carbon atoms. The alkyl (meth)acrylate is preferably an alkyl (meth)acrylate that can give a homopolymer satisfying a Tg of −80 to 60° C. from the viewpoint of endurance of the resultant laminated polarizing film against peeling in a drop test of this film, and the water resistance of the film. It is preferred to use, for example, the following: methyl acrylate (Tg: 8° C.), ethyl acrylate (Tg: −20° C.), n-propyl acrylate (Tg: 8° C.), n-butyl acrylate (Tg: −45° C.), isobutyl acrylate (Tg: −26° C.), t-butyl acrylate (Tg: 14° C.), isoamyl acrylate (Tg: −45° C.), cyclohexyl acrylate (Tg: 8° C.), 2-ethylhexyl acrylate (Tg: −55° C.), n-octyl acrylate (Tg: −65° C.), isooctyl acrylate (Tg: −58° C.), isononyl acrylate (Tg: −58° C.), or lauryl acrylate (Tg: 15° C.).
The active-energy-ray-curable adhesive composition according to the present invention may contain, as a radical polymerizable compound that is a monofunctional radical polymerizable compound, a (meth)acrylate having a hydroxyl group. The (meth)acrylate having a hydroxyl group may be a (meth)acrylate having a (meth)acryloyl group and a hydroxyl group. Specific examples of the (meth)acrylate having a hydroxyl group include 6-hydroxyhexyl (meth)acrylate, 8-hydroxyoctyl (meth)acrylate, 10-hydroxydecyl (meth)acrylate, 12-hydroxylauryl (meth)acrylate, and other hydroxyalkyl (meth)acrylates each having 2 to 12 carbon atoms; (4-hydroxymethylcyclohexyl)methyl acrylate, and other alicyclic-skeleton-containing and hydroxyl-group-containing monomers; and 2-hydroxy-3-phenoxypropyl acrylate (trade name: ARONIX M5700, manufactured by Toagosei Co., Ltd.) and other aromatic-ring-containing and hydroxyl-group-containing monomers. The (meth)acrylate having a hydroxyl group is preferably a (meth)acrylate that can give a homopolymer satisfying a Tg of −80 to 40° C. from the viewpoint of the endurance of the resultant laminated polarizing film against peeling in a drop test of this film. It is preferred to use, for example, hydroxyethyl acrylate (Tg: −15° C.), hydroxypropyl acrylate (Tg: −7° C.), or hydroxybutyl acrylate (Tg: −32° C.).
The (meth)acrylate having a hydroxyl group may be a (meth)acrylate having a large chain length between the hydroxyl group and its (meth)acryloyl group. When the chain length is large between the hydroxyl group and the (meth)acryloyl group, hydroxyl groups of molecules of this (meth)acrylate are more easily aligned to an adherend film so that adhesion based on the polarity of the hydroxyl groups is favorably given more effectively to the adhesive. The (meth)acrylate having a hydroxyl group in which between the hydroxyl group and its (meth)acryloyl group the chain length is large is preferably a hydroxyl-group-containing monofunctional (meth)acrylate having a weight-average molecular weight of 160 to 3000. The weight-average molecular weight of the hydroxyl-group-containing monofunctional (meth)acrylate is more preferably from 200 to 2000, most preferably from 300 to 1000. About the hydroxyl-group-containing monofunctional (meth)acrylate having a weight-average molecular weight of 160 to 3000, the chain length between the hydroxyl group and the (meth)acryloyl group is preferably large, and the hydroxyl group and the (meth)acryloyl group are present, respectively, at both terminals of the (meth)acrylate (having, in particular, a linear structure).
If the weight-average molecular weight of the (meth)acrylates having a hydroxyl group is too large, the active-energy-ray-curable adhesive becomes high in viscosity to give an uneven painted thickness so that the painted layer unfavorably becomes poor in external appearance, or in the bonding step, air bubbles enter the layer so that the layer unfavorably becomes poor in external appearance. Furthermore, the number of hydroxyl groups in this layer is relatively decreased so that the adhesive layer unfavorably does not gain an adhesion-giving effect based on the polarity of the hydroxyl groups with ease. Examples of the hydroxyl-group-containing monofunctional (meth)acrylate having a weight-average molecular weight of 160 to 3000 include any one that satisfies a weight-average molecular weight of 160 to 3000 out of the above-mentioned hydroxyalkyl (meth)acrylates, polyethylene glycol mono(meth)acrylate, polypropylene glycol mono(meth)acrylate, polyethylene glycol/polyethylene glycol mono(meth)acrylate, and other polyalkylene glycol mono(meth)acrylates; and caprolactone-modified products of any one of the above-mentioned hydroxyalkyl (meth)acrylates, and (4-hydroxymethylcyclohexyl)-methyl acrylate. The caprolactone-modified products are preferably caprolactone-added products of hydroxyethyl (meth)acrylate. The addition amount of caprolactone is particularly preferably 1 to 5 mol.
The proportion of the (meth)acrylate having a hydroxyl group is 70% or less by weight of the whole of the radical polymerizable compounds in the active-energy-ray-curable adhesive, the proportion of the compounds being 100% by weight, to cause the resultant laminated polarizing film to satisfy impact resistance, and heating buckling resistance. If this proportion is large, an effect of the hydrophilicity of the hydroxyl groups is increased so that the layer is unfavorably deteriorated in water resistance. Thus, for example, the layer is peeled off in a humidifying environment. In the case of using, as the (meth)acrylate having a hydroxyl group, a hydroxyalkyl (meth)acrylate or (4-hydroxymethylcyclohexyl)-methyl acrylate, the proportion thereof is preferably from 10 to 60% by weight, more preferably from 20 to 50% by weight. In the case of using, as the (meth)acrylate having a hydroxyl group, a hydroxyl-group containing monofunctional (meth)acrylate having a weight-average molecular weight of 160 to 3000, the proportion thereof is preferably from 1 to 70%, more preferably from 30 to 60% by weight of the whole of the radical polymerizable compounds in the active-energy-ray-curable adhesive composition, the proportion of the compounds being 100% by weight.
The active-energy-ray-curable adhesive composition according to the present invention preferably contains, as the radical polymerizable compound having a hydroxyl group, a compound represented by the following general formula (I):
wherein X is a functional group including a reactive group, and R1 and R2 each represent a hydrogen atom. When the active-energy-ray-curable adhesive composition contains the compound represented by the formula (I), adhesion water-resistance is very dramatically improved between an adhesive layer formed through/after the curing of the composition, and the polarizer or the transparent protective film subjected to activating treatment.
The group X, which the compound represented by the general formula (I) has, is a functional group including a reactive group, and is a functional group that can react with another curable component contained in the adhesive composition. Examples of the reactive group, which X includes, include hydroxyl, amino, aldehyde, carboxyl, vinyl, (meth)acryl, styryl, (meth)acrylamide, vinyl ether, epoxy, and oxetane groups. When the adhesive composition used in the present invention is active-energy-ray curable, the reactive group, which X includes, is preferably at least one reactive group selected from the group consisting of vinyl, (meth)acryl, styryl, (meth)acrylamide, vinyl ether, epoxy, oxetane, and mercapto groups. When the adhesive composition is, particularly, radical polymerizable, the reactive group, which X includes, is preferably at least one reactive group selected from the group consisting of (meth)acryl, styryl, and (meth)acrylamide groups. It is more preferred that the compound represented by the general formula (I) has a (meth)acrylamide group since the compound is high in reactivity to be increased in copolymerization rate in the active-energy-ray-curable adhesive composition. This case is preferred also since the (meth)acrylamide group is high in polarity so that the resultant adhesive is excellent in adhesion to produce the advantageous effects of the present invention effectively. When the adhesive composition used in the invention is cationic polymerizable, the reactive group, which X includes, has preferably at least one reactive group selected from the group consisting of hydroxyl, amino, aldehyde, carboxyl, vinyl ether, epoxy, oxetane, and mercapto groups. When the reactive group has, in particular, an epoxy group, adhesion between the resultant curable resin layer and an adherend is favorably excellent. When the reactive group has a vinyl ether group, the adhesive composition is favorably excellent in curability.
Preferred and specific examples of the compound represented by the general formula (I) include the following compounds (Ia) to (Id), in which X is a functional group including a reactive group bonded to a boron atom to interpose, therebetween, a phenylene or alkylene group:
In the present invention, the compound represented by the general formula (I) may be a compound in which a reactive group is bonded directly to a boron atom. However, as illustrated as the above-mentioned specific examples, it is preferred that the compound represented by the general formula (I) is a compound in which a reactive group and a boron atom are bonded to each other to interpose, therebetween, a phenylene or alkylene group, that is, that X is a functional group including a reactive group bonded to a boron atom to interpose, therebetween, a phenylene or alkylene group. When the compound represented by the general formula (I) is, for example, a compound in which X is bonded to a reactive group to interpose, therebetween, an oxygen atom bonded to a boron atom, an adhesive layer yielded by curing an adhesive composition including this compound tends to be deteriorated in adhesion water-resistance. In the meantime, when the compound represented by the general formula (I) is not a compound having a boron-oxygen atom, but a compound in which a boron atom is bonded to a phenylene group or alkylene group, so that while this compound has a boron-carbon bond, the compound contains a reactive group, the resultant adhesive layer is favorably improved in adhesion water-resistance. In the present invention, the compound represented by the general formula (I) is preferably a compound in which a reactive group and a boron atom may be bonded to each other to interpose, therebetween, an organic group which has 1 to 20 carbon atoms and may have a substituent since an adhesive layer yielded through/after the curing of the adhesive composition is also improved in adhesion water-resistance. The organic group, which has 1 to 20 carbon atoms and may have a substituent, is, for example, a linear or branched alkylene group which has 1 to 20 carbon atoms and may have a substituent, a cyclic alkylene group which has 3 to 20 carbon atoms and may have a substituent, a phenylene group which has 6 to 20 carbon atoms and may have a substituent, or a naphthylene group which has 10 to 20 carbon atoms and may have a substituent.
Examples of the compound represented by the general formula (I) include, besides the compounds given above as the examples thereof, an ester made from hydroxyethylacrylamide and boric acid, an ester made from methylolacrylamide and boric acid, an ester made from hydroxyethyl acrylate and boric acid, an ester made from hydroxybutyl acrylate and boric acid, and any other ester made from a (meth)acrylate and boric acid.
The content of the compound represented by the general formula (I) in the adhesive composition is preferably from 0.001 to 50%, more preferably from 0.1 to 30%, most preferably from 1 to 10% by weight to improve the adhesion between the polarizer and the curable resin layer, and the water resistance of the two and, in particular, to improve the adhesion and the water resistance when the polarizer is bonded to a transparent protective film through the adhesive layer.
The active-energy-ray-curable adhesive composition according to the present invention preferably contains, as the radical polymerizable compound having a hydroxyl group, a compound represented by the following general formula (II):
wherein X is a functional group including at least one reactive group selected from the group consisting of vinyl, (meth)acryl, styryl, (meth)acrylamide, vinyl ether, epoxy, oxetane, and mercapto groups, and R1 and R2 each represent a hydrogen atom. When the active-energy-ray-curable adhesive composition includes the compound represented by the general formula (II), adhesion water-resistance is very dramatically improved between an adhesive layer formed through/after the curing of the composition, and the polarizer or the transparent protective film subjected to activating treatment. The above-mentioned aliphatic hydrocarbon group is, for example, a linear or branched alkyl group which has 1 to 20 carbon atoms and may have a substituent, a cyclic alkyl group which has 3 to 20 carbon atoms and may have a substituent, or an alkenyl group which has 2 to 20 carbon atoms. The aryl group is, for example, a phenyl group which has 6 to 20 carbon atoms and may have a substituent, or a naphthyl group which has 10 to 20 carbon atoms and may have a substituent. The heterocyclic group is, for example, a 5-membered or 6-membered group which contains at least one heteroatom, and may have a substituent. These may be linked to each other to form a ring.
The functional group X, which the compound represented by the general formula (II) has, contains a reactive group. Examples of the reactive group include hydroxyl, amino, aldehyde, carboxyl, vinyl, (meth)acryl, styryl, (meth)acrylamide, vinyl ether, epoxy, oxetane groups. When the curable resin composition used in the present invention is active-energy-ray curable, the reactive group X is preferably at least one reactive group selected from the group consisting of vinyl, (meth)acryl, styryl, (meth)acrylamide, vinyl ether, epoxy, and oxetane groups. When the curable resin composition is, particularly, radical polymerizable, the reactive group is at least one reactive group selected from the group consisting of (meth)acryl, styryl, and (meth)acrylamide groups. More preferably, the compound represented by the general formula (II) has a (meth)acrylamide group since the compound is high in reactivity to be increased in copolymerization rate in the active-energy-ray-curable adhesive composition. Moreover, this case is preferred also since the (meth)acrylamide group is high in polarity so that the resultant adhesive is excellent in adhesion. Consequently, the advantageous effects of the present invention can be effectively gained. When the curable resin layer used in the present invention is cationic polymerizable, the reactive group X preferably has at least one functional group selected from the group consisting of hydroxyl, amino, aldehyde, carboxyl, vinyl ether, epoxy, oxetane, and mercapto groups. When the reactive group X has, particularly, an epoxy group, the adhesion between the resultant curable resin layer and an adherend is favorably excellent. When the reactive group has a vinyl ether group, the curable resin composition is favorably excellent in curability.
When the functional group X, which the compound represented by the general formula (II) has, is a functional group represented by the following general formula (III):
wherein, R3 is a hydrogen atom or a methyl radical, and n is an integer of 1 to 4, a cure resin layer yielded by curing the curable resin composition containing the crosslinking agent is excellent in compatibility with a water-soluble resin, such as polyvinyl alcohol, so that an active-energy-ray-curable functional group, such as a (meth)acryloyl group, can be effectively introduced into the water-soluble resin. Additionally, when the curable resin layer containing the crosslinking agent is located to contact the water-soluble resin, this layer is excellent in adhesion to the water-soluble resin. In the general formula (III), R3 is a hydrogen atom or a methyl group. R3 is preferably a hydrogen atom since the resultant composition is excellent in curability. In the formula (III), n is preferably from 1 to 4. If n is 5 or more, the compound is lowered in compatibility with the water-soluble resin so that a crosslinked structure of the water-soluble resin, which is an advantageous effect of the present invention, is not easily gained, or the distance between crosslinked points in the structure becomes long so that the adhesive layer does not unfavorably gain water resisting effect with ease. The compound represented by the general formula (III) is in particular preferably an ester made from hydroxyethyl acrylate and boric acid, or an ester made from hydroxybutyl acrylate and boric acid.
Also when the functional group X, which the compound represented by the general formula (II) has, is a functional group represented by the following general formula (IV):
wherein R3 is a hydrogen atom or a methyl group, and m is an integer of 1 to 4, the following is attained in the same way as described above: a cure resin layer yielded by curing the curable resin layer containing the crosslinking agent is excellent in compatibility with a water-soluble resin, such as polyvinyl alcohol, so that an active-energy-ray-curable functional group, such as a (meth)acryloyl group, can be effectively introduced into the water-soluble resin; and additionally, when the curable resin layer containing the crosslinking agent is located to contact the water-soluble resin, this layer is excellent in adhesion to the water-soluble resin. In the general formula (IV), R3 is a hydrogen atom or a methyl group. R3 is preferably a hydrogen atom since the resultant composition is excellent in curability. In the formula (3), n is preferably from 1 to 4. If n is 5 or more, the compound is lowered in compatibility with the water-soluble resin so that a crosslinked structure of the water-soluble resin, which is an advantageous effect of the present invention, is not easily gained, or the distance between the crosslinked points becomes long so that the adhesive layer does not unfavorably gain water resisting effect with ease. The compound represented by the general formula (3) is in particular preferably an ester made from hydroxyethyl acrylate and boric acid, or an ester made from hydroxybutyl acrylate and boric acid.
When the compound represented by the general formula (II) is incorporated into the curable resin composition and the resultant is used as an adhesive for a water-soluble resin film, the compound represented by the general formula (II) is incorporated into the resin composition in a proportion that is preferably 0.01% or more, more preferably 1% or more by weight. About the compound represented by the general formula (II), its borate group acts onto a surface of the water-soluble resin film; thus, a very small addition amount thereof allows to produce an effect of improving adhesion between the composition and the film. However, if the content by proportion thereof is too small, the adhesion-improving effect is not easily gained. The upper limit of the proportion of the compound represented by the general formula (II) in the curable resin composition is, for example, 80% by weight. The proportion is preferably 50% or less, more preferably 30% or less, most preferably 10% or less by weight. The compound represented by the general formula (II) is usable alone as an adhesive for a water-soluble resin film.
The weight-average molecular weight of the hydroxyl-group-containing monofunctional (meth)acrylate is measurable by GPC (gel permeation chromatography). Detector: differential refractometer (RI), and standard sample: polystyrene.
The active-energy-ray-curable adhesive composition according to the present invention may include, as a radical polymerizable compound, a radical polymerizable compound different from the above-mentioned radical polymerizable compounds
The proportion of the different radical polymerizable compound is preferably 40% or less by weight of the whole of the radical polymerizable compounds in the active-energy-ray-curable adhesive composition, the proportion of the compounds being 100% by weight, from the viewpoint of the adhesion, the endurance and the water resistance of the adhesive layer. The proportion is preferably from 2 to 25%, more preferably from 5 to 20% by weight.
The active-energy-ray-curable adhesive composition according to the present invention may contain a si lane coupling agent besides the radical polymerizable compounds. The silane coupling agent is preferably a silane coupling agent having no radical polymerizable functional group. The silane coupling agent having no radical polymerizable functional group acts on a surface of the polarizer to give a higher water resistance to the polarizer.
A specific example of the silane coupling agent having no radical polymerizable functional group is a silane coupling agent having an amino group. Specific examples of the silane coupling agent having an amino group include γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ-aminopropyltriisopropoxysilane, γ-aminopropylmethyldimethoxysilane, γ-aminopropylmethyldiethoxysilane, γ-(2-aminoethyl)aminopropyltrimethoxysilane, γ-(2-aminoethyl)aminopropylmethyldimethoxysilane, γ-(2-aminoethyl)aminopropyltriethoxysilane, γ-(2-aminoethyl)aminopropylmethyldiethoxysilane, γ-(2-aminoethyl)aminopropyltriisopropoxysilane, γ-(2-(2-aminoethyl)aminoethyl)aminopropyltrimethoxysilane, γ-(6-aminohexyl)aminopropyltrimethoxysilane, 3-(N-ethylamino)-2-methylpropyl trimethoxysilane, γ-ureidopropyltrimethoxysilane, γ-ureidopropyltriethoxysilane, N-phenyl-γ-aminopropyl trimethoxysilane, N-benzyl-γ-aminopropyl trimethoxysilane, N-vinylbenzyl-γ-aminopropyltriethoxysilane, N-cyclohexylaminomethyltriethoxysilane, N-cyclohexylaminomethyldiethoxymethylsilane, N-phenylaminomethyltrimethoxysilane, (2-aminoethyl)aminomethyltrimethoxysilane, N,N′-bis[3-(trimethoxysilyl)propyl]ethylenediamine, and other amino-group-containing silanes; and N-(1,3-dimethylbutylidene)-3-(triethoxysilyl)-1-propaneamine, and other ketimines type silanes.
The silane coupling agent having an amino group is preferably γ-aminopropyl trimethoxysilane, γ-(2-aminoethyl)aminopropyltrimethoxysilane, γ-(2-aminoethyl)aminopropylmethyldimethoxysilane, γ-(2-aminoethyl)aminopropyltriethoxysilane, γ-(2-aminoethyl)aminopropylmethyldiethoxysilane, or N-(1,3-dimethylbutylidene)-3-(triethoxysilyl)-1-propanamine.
Specific examples of the silane coupling agent which has no radical polymerizable functional group and which is other than the silane coupling agent having an amino group include 3-chloropropyltrimethoxysilane, 3-mercaptopropylmethyldimethoxysilane, 3-mercaptopropyltrimethoxysilane, bis(triethoxysilylpropyl) tetrasulfide, 3-isocyanatopropyltriethoxysilane, and imidazolesilane.
Examples of a silane coupling agent as an active-energy-ray-curable compound include vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxysilane, 2-(3,4 epoxycyclohexyl) ethyl trimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, 3-glycidoxypropyltriethoxysilane, p-styryltrimethoxysilane, 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3-methacryloxypropyltriethoxysilane, and 3-acryloxypropyl trimethoxysilane.
Such silane coupling agents may be used singly or in any combination of two or more thereof. The blend amount of the silane coupling agent having no radical polymerizable functional group is usually 20 parts or less, preferably from 0.01 to 20 parts, more preferably from 0.05 to 15 parts, even more preferably from 0.1 to 10 parts by weight for 100 parts by weight of the whole of the radical polymerizable compounds in the active-energy-ray-curable adhesive. If the blend amount is more than 20 parts or more by weight, the adhesive may be unfavorably deteriorated in storability.
The active-energy-ray-curable adhesive composition according to the present invention may contain, besides the radical polymerizable compounds, an acrylic oligomer yielded by polymerizing a (meth)acrylic monomer. The matter that the active-energy-ray-curable adhesive contains the acrylic oligomer allows to decrease a curing shrinkage of the composition when the composition is irradiated with an active energy ray to be cured, so as to decrease interfacial stress between the adhesive, and adherends such as the polarizing film (P) and the optical film(s) (3). Consequently, the adhesion between the adhesive layer and the adherends can be restrained from being lowered.
The active energy ray-curable adhesive is preferably low in viscosity, considering the workability and uniformity thereof when the adhesive is painted. Thus, the acrylic oligomer yielded by polymerizing a (meth)acrylic monomer is also preferably low in viscosity. The acrylic oligomer that is low in viscosity and can prevent a curing shrinkage of the resultant adhesive layer is preferably an oligomer having a weight-average molecular weight (Mw) of 15000 or less. The weight-average molecular weight is more preferably 10000 or less, in particular preferably 5000 or less. In the meantime, in order to restrain a curing shrinkage of the cured product layer (adhesive layer) sufficiently, the weight-average molecular weight (Mw) of the acrylic oligomer is preferably 500 or more, more preferably 1000 or more, in particular preferably 1500 or more. Specific examples of the (meth)acrylic monomer, from which the acrylic oligomer is made, include 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, 2-ethylhexyl (meth)acrylate, 4-methyl-2-propylpentyl (meth)acrylate, N-octadecyl (meth)acrylate, and other alkyl (meth)acrylates (1-20 carbon atoms); cycloalkyl (meth)acrylates (such as cyclohexyl (meth)acrylate, and cyclopentyl (meth)acrylate); aralkyl (meth)acrylates (such as benzyl (meth)acrylate); polycyclic (meth)acrylate (such as 2-isobornyl (meth)acrylate, 2-norbornylmethyl (meth)acrylate, 5-norbornene-2-yl-methyl (meth)acrylate, and 3-methyl-2-norbornylmethyl (meth)acrylate); hydroxyl-group-containing (meth)acrylates (such as hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, and 2,3-dihydroxypropylmethyl-butyl (meth)acrylate); 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, ethylcarbitol (meth)acrylate, and phenoxyethyl (meth)acrylate); epoxy-group-containing (meth)acrylates (such as glycidyl (meth)acrylate); halogen-containing (meth)acrylates (such as 2,2,2-trifluoroethyl (meth)acrylate, 2,2,2-trifluoroethyl (meth)acrylate, tetrafluoropropyl (meth)acrylate, hexafluoropropyl (meth)acrylate, octafluoropentyl (meth)acrylate, and heptadecafluorodecyl (meth)acrylate); and alkylaminoalkyl (meth)acrylates (such as dimethylaminoethyl (meth)acrylate). These (meth)acrylates may be used singly or in any combination of two or more thereof. Specific examples of the acrylic oligomer (E) include products “ARUFON” manufactured by Toagosei Co., Ltd., “ACTFLOW” manufactured by Soken Chemical & Engineering Co., Ltd., and “JONCRYL” manufactured by BASF Japan Ltd.
Usually, the blend amount of the acrylic oligomer is preferably 30 parts or less by weight for 100 parts by weight of the radical polymerizable compounds in the active-energy-ray-curable adhesive. If the content of the acrylic oligomer in the composition is too large, the reaction rate is intensely lowered when the composition is irradiated with an active energy ray, so that the curing of the composition may become poor. In the meantime, in order to restrain a curing shrinkage of the cured product layer (adhesive layer “a”) sufficiently, the composition contains the acrylic oligomer in an amount that is preferably 3 parts or more, more preferably 5 parts or more by weight.
The active-energy-ray-curable adhesive composition according to the present invention may further contain, besides the radical polymerizable compounds, a radical polymerizable compound having an active methylene group, and a radical polymerization initiator having hydrogen-withdrawing effect. This structure makes a remarkable improvement of the adhesive layer in adhesion even immediately after the laminated polarizing film is taken out, particularly, from a high-humidity environment or water (even when the film is in a non-dry state). Reasons therefor are unclear. However, the improvement would be based on the following causes: While the radical polymerizable compound having an active methylene group is polymerized together with the other radical polymerizable compounds that will be included in the adhesive layer, the compound is taken into a main chain and/or side chains of a base polymer in the adhesive layer to form the adhesive layer. In this polymerizing step, in the presence of the radical polymerization initiator having hydrogen-withdrawing effect, the base polymer, which will be included in the adhesive layer, is formed and simultaneously hydrogen is withdrawn from the active-methylene-having radical polymerizable compound to generate radicals in methylene groups of molecules of the compound. The methylene groups in which radicals are generated react with hydroxyl groups of the polarizer, such as ones of PVA, so that covalent bonds are formed between the adhesive layer and the polarizer. Consequently, the adhesive layer which the polarizing film has would be remarkably improved in adhesion even when the laminated polarizing film is, particularly, in a non-dry state.
The radical polymerizable compound having an active methylene group is a compound that has, at a terminal or molecule thereof, an active double bond group such as a (meth)acryl group, and that has an active methylene group. Examples of the active methylene group include acetoacetyl, alkoxymalonyl, and cyanoacetyl groups. Specific examples of the radical polymerizable compound having an active methylene group include 2-acetoacetoxyethyl (meth)acrylate, 2-acetoacetoxypropyl (meth)acrylate, 2-acetoacetoxyethyl-1-methylethyl (meth)acrylate, and other acetoacetoxyalkyl (meth)acrylates; and 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 polymerization initiator having hydrogen-withdrawing effect is, for example, a thioxanthone-based radical polymerization initiator, or a benzophenone-based radical polymerization initiator. The thioxanthone-based radical polymerization initiator may be a compound represented by the following general formula (1):
wherein R1 and R2 are each —H, —CH2bH3, -iPr or Cl, and R1 and R2 may be the same as or different from each other.
Specific examples of the compound represented by the general formula (1) include thioxanthone, dimethyithioxanthone, diethylthioxanthone, isopropylthioxanthone, and chlorothioxanthone. Out of compounds each represented by the general formula (1), particularly preferred is diethylthioxanthone, in which R1 and R2 are each —CH2bH3.
Besides the photopolymerization initiator of the general formula (1), the active-energy-ray-curable adhesive preferably further contains, as a photopolymerization initiator, a compound represented by the following general formula (2):
wherein R3, R4 and R5 each represent —H, —CH3bH2bH3, -iPr or Cl, and R3, R4 and R5 may be the same as or different from each other. The use of the respective photopolymerization initiators represented by the general formulae (1) and (2) makes the reaction high in efficiency by photosensitizing-reaction of these initiators to improve the adhesive layer, in particular, in adhesion.
As described above, in the present invention, a radical is generated in a methylene group of the active-methylene-group-having radical polymerizable compound in the presence of the radical polymerization initiator having hydrogen-withdrawing effect. This methylene group reacts with a hydroxyl group to form a covalent bond. Thus, in order to generate radicals in the methylene groups of molecules of the active-methylene-group-having radical polymerizable compound to form covalent bonds sufficiently, the active-methylene-group-having radical polymerizable compound is incorporated into the active-energy-ray-curable adhesive into an amount preferably from 1 to 30 parts by weight, more preferably from 3 to 30 parts by weight for 100 parts by weight of the whole of the radical polymerizable compounds in the adhesive. If the amount of the active-methylene-group-having radical polymerizable compound is less than 1 part by weight, the adhesion-improving effect is low when the adhesive is in a non-dry state so that the adhesive may not be sufficiently improved in water resistance. If the amount is more than 50 parts by weight, the adhesive layer may be poorly cured. The amount of the radical polymerization initiator having hydrogen-withdrawing effect is contained in the active-energy-ray-curable adhesive in an amount preferably from 0.1 to 10 parts, more preferably from 0.3 to 9 parts by weight for 100 parts by weight of the whole of the radical polymerizable compounds in the adhesive. If the amount of the radical polymerization initiator having hydrogen-withdrawing effect is less than 0.1 parts by weight, the hydrogen-withdrawing reaction may not sufficiently advance. If the amount is more than 10 parts by weight, the initiator may not be completely dissolved in the composition.
The active-energy-ray-curable adhesive composition may contain an optically acid-generating agent. When the active-energy-ray-curable adhesive composition contains the optically acid-generating agent, the adhesive layer can be dramatically made higher in water resistance and endurance than when the composition contains no optically acid-generating agent. The optically acid-generating agent may be represented by the following general formula (3).
L+X− [Formula 8]
wherein L+ represents an onium cation, and X− represents a counter anion selected from the group consisting of PF6−, SbF6−, AsF6−, Sbcl6−, BiCl5−, SnCl6−, ClO4−, a dithiocarbamate anion, and SCN−.
The following will describe the counter ion X− in the general formula (3).
The counter ion X− in the general formula (3) is not particularly limited in principle. The ion is preferably a non-nucleophilic anion. When the counter ion X− is the non-nucleophilic anion, a nucleophilic reaction is not easily caused in a cation coexisting in the molecule of the optically acid-generating agent, or in various materials used together. Consequently, an improvement can be made in stability, over time, of the optically acid-generating agent itself, which is represented by the general formula (2), and a composition using this agent. The non-nucleophilic anion denotes an anion low in power for causing nucleophilic reaction. Examples of such an anion include PF6−, SbF6−, AsF6−, SbCl6−, BiCl5−, SnCl6−, ClO4−, a dithiocarbamate anion, and SCN−.
Specific examples of the optically acid-generating agent include “CYRACURE UVI-6992”, and “CYRACURE UVI-6974” (each manufactured by Dow Chemical Japan Ltd.), “ADEKA OPTOMER SP150”, “ADEKA OPTOMER SP152”, “ADEKA OPTOMER SP170”, and “ADEKA OPTOMER SP172” (each manufactured by ADEKA CORPORATION), “IRGACURE 250” (manufactured by Ciba Specialty Chemicals Co., Ltd.), “CI-5102”, and “CI-2855” (each manufactured by Nippon Soda Co., Ltd.), “SAN-AID SI-60L”, “SAN-AID SI-80L”, “SAN-AID SI-100L”, “SAN-AID SI-110L”, and “SAN-AID SI-180L” (each manufactured by Sanshin Chemical Industry Co., Ltd.), “CPI-100P” and “CPI-100A” (each manufactured by San-Apro Ltd.), and “WPI-069”, “WPI-113”, “WPI-116”, “WPI-041”, “WPI-044”, “WPI-054”, “WPI-055”, “WPAG-281”, “WPAG-567”, and “WPAG-596” (each manufactured by Wako Pure Chemical Industries, Ltd.).
The content of the optically acid-generating agent is 10% or less, preferably from 0.01 to 10%, more preferably from 0.05 to 5%, in particular preferably from 0.1 to 3% by weight of the whole of the curable resin composition.
In the active-energy-ray-curable adhesive, it is preferred to use the optically acid-generating agent together with a compound containing either an alkoxy group or an epoxy group in the active-energy-ray-curable adhesive.
In the case of using a compound having in the molecule thereof one or more epoxy groups, or a polymer having in the molecule thereof two or more epoxy groups (epoxy resin), it is allowable to use a compound having in the molecule thereof two or more functional groups each reactive with an epoxy group. Examples of the functional groups each reactive with an epoxy group include carboxyl, phenolic hydroxyl, mercapto, and primary or secondary aromatic amino groups. About these functional groups, the compound or the polymer in particular preferably has in one molecule thereof two or more of the groups, considering the three-dimensional curability of the adhesive.
The polymer having in the molecule one or more epoxy groups is, for example, an epoxy resin. Examples thereof include bisphenol A type epoxy resin derived from bisphenol A and epichlorohydrin, bisphenol F type epoxy resin derived from bisphenol F and epichlorohydrin, bisphenol S type epoxy resin, phenol novolak type epoxy resin, cresol novolak type epoxy resin, bisphenol A novolak type epoxy resin, bisphenol F novolak type epoxy resin, alicyclic epoxy resins, diphenyl ether type epoxy resins, hydroquinone type epoxy resins, naphthalene type epoxy resins, biphenyl type epoxy resins, fluorene type epoxy resins, polyfunctional epoxy resins such as trifunctional epoxy resins and tetrafunctional epoxy resins, glycidylester type epoxy resins, glycidylamine type epoxy resins, hydantoin type epoxy resins, isocyanurate type epoxy resins, and linear aliphatic epoxy resins. These epoxy resins may be halogenated, or hydrogenated. Examples of commercially available epoxy resin products include products JER COATs 828, 1001, 801N, 806, 807, 152, 604, 630, 871, YX8000, YX8034, and YX4000 manufactured by Japan Epoxy Resins Co., EPICHLON830, EXA835LV, HP4032D, and HP820 manufactured by DIC Corp., EP4100 series, EP4000 series, and EPU series manufactured by ADEKA CORPORATION, CELLOXIDE series (2021, 2021P, 2083, 2085, and 3000), EPOLEAD series, and EHPE series, manufactured by Daicel Corp., YD series, YDF Series, YDCN series, YDB series, phenoxy resins (for example, YP series: polyhydroxy polyethers each synthesized from a bisphenol and epichlorohydrin, and each having, at both terminals thereof, epoxy groups, respectively) manufactured by Nippon Steel Chemical Co., Ltd., DENACOL series manufactured by Nagase ChemteX Corp., and EPOLIGHT series manufactured by Kyoeisha Chemical Co., Ltd. However, the epoxy resin products are not limited to these examples. These epoxy resins may be used in combination of two or more thereof. When the glass transition temperature Tg of the adhesive layer is calculated, any compound and any polymer (H) that each have an epoxy group are not considered for the calculation.
The compound having in the molecule thereof an alkoxyl group is not particularly limited as far as the compound is a compound having in the molecule thereof one or more alkoxyl groups. The compound may be a known compound. Typical examples of such a compound include melamine compounds, and amino resins.
The blend amount of the compound having either an alkoxy group or an epoxy group is usually 30 parts or less by weight for 100 parts by weight of the whole of the radical polymerizable compounds in the active-energy-ray-curable adhesive. If the content of the compound in the composition is too large, the adhesive layer may be lowered in adhesion, and the resultant laminated polarizing film may be deteriorated, in a drop test, in impact resistance. The content of the compound in the composition is more preferably 20 parts or less by weight. In the meantime, the composition contains the compound in an amount that is preferably 2 parts or more, more preferably 5 parts or more from the viewpoint of the water resistance of the cured product layer (the adhesive layer(s) 2a).
When the active-energy-ray-curable adhesive composition according to the present invention is used in an electron curable form, it is not particularly necessary to incorporate any photopolymerization initiator into the composition. However, when the composition is used in an ultraviolet curable form, a photopolymerization initiator is preferably used, and a photopolymerization initiator high in sensitivity to light rays of 380 nm or more wavelengths is in particular preferably used. The photopolymerization initiator high in sensitivity to light rays of 380 nm or more wavelengths is to be detailed later.
In the active-energy-ray-curable adhesive composition according to the present invention, it is preferred to use, as a photopolymerization initiator, the compound represented by the general formula (1) singly:
wherein R1 and R2 are each —H, —CH2bH3, -iPr or Cl, and R1 and R2 may be the same as or different from each other; or use the compound represented by the general formula (1) together with the photopolymerization initiator high in sensitivity to light rays of 380 nm or more wavelengths, which is to be detailed later. In the case of using the compound represented by the general formula (1), the resultant adhesive layer is better in adhesion than in the case of using singly the photopolymerization initiator high in sensitivity to light rays of 380 nm or more wavelengths. Out of compounds each represented by the general formula (1), particularly preferred is diethylthioxanthone, in which R1 and R2 are each —CH2bH3. About the composition proportion of the compound represented by the general formula (1) in the composition, the amount of the compound is preferably from 0.1 to 5.0 parts, more preferably from 0.5 to 4.0 parts, even more preferably from 0.9 to 3.0 parts by weight for 100 parts by weight of the whole of the radical polymerizable compounds in the active-energy-ray-curable adhesive.
As required, a polymerization initiation aid is preferably added to the composition. Examples of the polymerization initiation aid include triethylamine, diethylamine, N-methyldiethanolamine, ethanolamine, 4-dimethylaminobenzoic acid, methyl 4-dimethylaminobenzoate, ethyl 4-dimethylaminobenzoate, and isoamyl 4-dimethylaminobenzoate. Particularly preferred is ethyl 4-dimethylaminobenzoate. When the polymerization initiation aid is used, the addition amount thereof is usually from 0 to 5 parts, preferably from 0 to 4 parts, most preferably from 0 to 3 parts by weight for 100 parts by weight of the whole of the radical polymerizable compounds.
As required, a known photopolymerization initiator may be together used. The photopolymerization initiator is preferably a photopolymerization initiator high in sensitivity to light rays of 380 nm or more wavelengths. Specific examples thereof include 2-methyl-1-(4-methylthiophenyl)-2-morpholinopropane-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(H5-2,4-cyclopentadiene-1-yl)-bis(2,6-difluoro-3-(1H-pyrrol-1-yl)-phenyl) titanium.
Besides the photopolymerization initiator of the general formula (1), it is preferred to use a compound represented by the following general formula (2) further:
wherein R3, R4 and R5 each represent —H, —CH3bH2bH3, -iPr or Cl, and R3, R4 and R5 may be the same as or different from each other. The compound represented by the general formula (2) is preferably 2-methyl-1-(4-methylthiophenyl)-2-morpholinopropane-1-one, which is also a commercially available product (trade name: IRGACURE 907, manufacturer: the company BASF). Furthermore, the following are preferred because of a high sensitivity thereof: 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1 (trade name: IRGACURE 369, manufacturer: the company BASF), 2-(dimethylamino)-2-[(4-methylphenyl)methyl]-1-[4-(4-morpholinyl)phenyl]-1-butanone (trade name: IRGACURE 379, manufacturer: the company BASF).
As far as the objects and the advantageous effects of the present invention are not damaged, various additives may be blended, as other optional components, into the active-energy-ray-curable adhesive composition according to the present invention. Examples of the additives include epoxy resins, polyamides, polyamideimides, polyurethanes, polybutadienes, polychloroprenes, polyethers, polyesters, styrene-butadiene block copolymers, petroleum resins, xylene resins, ketone resins, cellulose resins, fluorine-containing oligomers, silicone-based oligomers, polysulfide-based oligomers, and other polymers or oligomers; phenothiazine, 2,6-di-T-butyl-4-methylphenol, and other polymerization inhibitors; polymerization initiation aids; leveling agents; wettability improvers; surfactants; plasticizers; ultraviolet absorbers; inorganic fillers; pigments; and dyes.
The active-energy-ray-curable adhesive according to the present invention is irradiated with an active energy ray to be cured, so that the adhesive layer(s) (a) can be formed.
The active energy ray may be an electron beam, or rays including visible rays in a wavelength range from 380 to 450 nm. For reference, a long-wavelength limit of visible rays is about 780 nm. However, visible rays having a wavelength more than 450 nm do not contribute to absorption into any polymerization initiator, and further the rays may cause the generation of heat. It is therefore preferred in the present invention to use a bandpass filter to block longer-wavelength visible rays of 450 nm or more wavelengths.
Conditions for the radiation of the electron beam are arbitrary-selected appropriate conditions as far as the conditions are capable of curing the active-energy-ray-curable adhesive. For example, in the radiation of the electron beam, the accelerating voltage is preferably from 5 to 300 kV, more preferably from 10 to 250 kV. If the accelerating voltage is less than 5 kV, the electron beam may not unfavorably reach the adhesive layer so that the adhesive layer may be poorly cured. If the accelerating voltage is more than 300 kV, the penetrating power of the beam into a sample is too strong so that its polarizing film (P) and its optical film(s) (3) may be damaged. The radiated ray quantity is from 5 to 100 kGy, preferably from 10 to 75 kGy. If the radiated ray quantity is less than 5 kGy, the adhesive is insufficiently cured. If the quantity is more than 100 kGy, the polarizing film (P) and the optical film(s) (3) are damaged. Thus, the laminated polarizing film is lowered in mechanical strength and is yellowed so that this film cannot gain desired optical properties.
The electron beam is usually radiated in an inert gas. If necessary, the radiation may be performed in the atmospheric air or under a condition that a small quantity of oxygen is introduced into the gas. An appropriate introduction of oxygen dares to cause oxygen blocking in a surface of (one of) the transparent protective film(s) onto which the electron beam is initially radiated, so that the beam can be prevented from damaging the transparent protective film to radiate the electron beam effectively only to the adhesive although this matter depends on the material of the transparent protective film(s).
In order to heighten the adhesive performance of the adhesive layer (a) between the polarizing film (P) and (each of) the optical film(s) (3), and simultaneously prevent the polarizing film (P) from being curled, it is preferred to use, as active energy rays, rays including visible rays in a wavelength range from 380 to 450 nm, particularly, active energy rays about which the radiation quantity of visible rays in a wavelength range from 380 to 450 nm is the largest. In the case of using one or more films to which ultraviolet absorbing power is given (one or more ultraviolet impermeable films) as the transparent protective film(s) of the polarizing film (P) or the optical film(s) (3), light rays having wavelengths shorter than 380 nm that have been absorbed in the transparent protective film(s) or the optical film(s) are converted to heat, so that heat is generated from the transparent protective film(s) or the optical film(s) (3). This matter causes curling, wrinkles and other defects of the laminated polarizing film. It is therefore preferred in the present invention to use, as an active energy ray generator, a device from which light rays having wavelengths shorter than 380 nm are not generated. More specifically, the ratio between the integrated illuminance of rays in a wavelength range from 380 to 440 nm to that of rays in a wavelength range from 250 to 370 nm is preferably from 100:0 to 100:50, more preferably from 100:0 to 100:40. For an active energy ray satisfying such an integrated illuminance relationship, preferred is a gallium sealed metal halide lamp or an LED light source which emits rays in a wavelength range from 380 to 440 nm. Alternatively, it is allowable to use, as a light source, a low pressure mercury lamp, a middle pressure mercury lamp, a high pressure mercury lamp, a super high pressure mercury lamp, an incandescent lamp, a xenon lamp, a halogen lamp, a carbon arc lamp, a metal halide lamp, a fluorescent lamp, a tungsten lamp, a gallium lamp, an excimer laser, or sunlight; block, out of rays emitted therefrom, rays having wavelengths shorter than 380 nm through a bandpass filter; and use the resultant rays. In order to heighten the adhesive performance of the adhesive layer (a) between the polarizing film (P) and (each of) the optical film(s) (3), and simultaneously prevent the polarizing film from being curled, it is preferred to use active energy rays obtained using a bandpass filter capable of blocking light rays of wavelengths shorter than 400 nm, or active energy rays of 405 nm wavelength that is obtained using an LED light source.
About the visible-ray-curable form, it is preferred to heat the active-energy-ray-curable adhesive before the radiation of visible rays (heating before radiation). In this case, the adhesive is heated preferably to 40° C. or higher, more preferably to 50° C. or higher. It is also preferred to heat the active-energy-ray-curable adhesive after the radiation of visible rays (heating after radiation) In this case, the adhesive is heated preferably to 40° C. or higher, more preferably to 50° C. or higher.
By incorporating the photopolymerization initiator represented by the general formula (1) into the active-energy-ray-curable adhesive related to the adhesive layer (a) or each of the adhesive layers (a), the adhesive layer (a) can be cured and formed when ultraviolet rays are radiated across the (corresponding) optical film (3) having UV absorbing power. The optical film (3) may be an optical film having a light transmittance less than 5% at a wavelength of 365 nm.
The method for giving UV absorbing power to the optical film (3) is, for example, a method of incorporating an ultraviolet absorbent into the optical film (3), or a method of laminating a surface treatment layer containing an ultraviolet absorbent onto a surface of the optical film (3).
Specific examples of the ultraviolet absorbent include oxybenzophenone-based compounds, benzotriazole-based compounds, salicylate-based compounds, benzophenone-based compounds, cyanoacrylate-based compounds, nickel complex compounds, and triazine-based compounds that are known in the prior art.
A method for producing the laminated polarizing film according to the present invention includes:
a painting step of painting an active-energy-ray-curable adhesive for forming the adhesive layer (a) to at least one surface of the transparent protective film (2) on a side of the polarizing film (P) on which the adhesive layer (a) is laminated, and the optical film (3),
a bonding step of causing the polarizing film (P) and the optical film (3) to bond each other, and
an adhering step of radiating the active energy ray to the resultant workpiece to cure the active-energy-ray-curable adhesive to cause the polarizing film (P) and the optical film (3) to adhere onto each other through the resultant adhesive layer (a).
In the polarizing film (P), the transparent protective film (2) and the optical film (3) may be subjected to a surface modifying treatment before the painting of the active-energy-ray-curable adhesive. Specific examples of the treatment include corona treatment, plasma treatment, saponifying treatment, excimer treatment, and flame treatment.
The means for painting the active-energy-ray-curable adhesive is appropriately selected in accordance with the viscosity of the composition, and a target thickness of the resultant. Examples of the painting means include a reverse coater, a gravure coater (direct, reverse or offset), a bar reverse coater, a roll coater, a die coater, a bar coater, and a rod coater. Additionally, for the painting, a dipping manner or the like is usable.
The polarizing film (P) and the optical film (3) are bonded to each other through the adhesive painted as described above. The adhering between the polarizing film (P) and the optical film (3) can be attained, using, for example, a roll laminator.
After the bonding between the polarizing film (P) and the optical film (3), an energy ray (such as an electron beam, an ultraviolet ray, or a visible ray) is radiated onto the workpiece to cure the active-energy-ray-curable adhesive to form an adhesive layer (a). A direction along which the active energy ray (which is, for example, an electron beam, an ultraviolet ray or a visible ray) is radiated may be any appropriate radiating direction. Preferably, the active energy ray is radiated from the optical film (3) side of the workpiece. If the active energy ray is radiated from the polarizing film (P) side thereof, the polarizing film (P) may be unfavorably deteriorated by the active energy ray (which is, for example, an electron beam, an ultraviolet ray or a visible ray).
When the laminated polarizing film according to the present invention is produced in a continuous line, the line speed, which depends on the curing period of the adhesive, is preferably from 1 to 500 m/min., more preferably from 5 to 300 m/min., even more preferably from 10 to 100 m/min. If the line speed is too small, the producing system is small in productivity, or the polarizing film (P) and the optical film (3) are excessively damaged so that a polarizing film which can endure an endurance test and others cannot be produced. If the line speed is too large, the adhesive is insufficiently cured so that the adhesive may not gain a target adhesion.
As described above, in the polarizing film (P), the transparent protective film (2) is laid on/over at least one surface of the polarizer (1) through the adhesive layer (a) or the adhesive layer (b).
The polarizer is not particularly limited, and may be of various types. The polarizer is, for example, a polarizer yielded by causing a dichroic material such as iodine or dichroic dye to be adsorbed into a hydrophilic polymeric film, such as a polyvinyl alcohol-based film, a partially-formal-converted polyvinyl alcohol-based film or an ethylene/vinyl acetate copolymer-based partially saponified film, and then stretching the resultant uniaxially; or a polyene-based aligned film made of, for example, a polyvinyl alcohol dehydrated-product or a polyvinyl chloride de-hydrochloride-treated-product. Out of such polarizers, preferred is a polarizer composed of a polyvinyl alcohol film and a dichroic substance such as iodine. The thickness of such a polarizer is preferably from 2 to 30 μm, more preferably from 4 to 20 μm, most preferably from 5 to 15 μm. If the thickness of the polarizer is small, the polarizer is unfavorably lowered in optical endurance. If the thickness of the polarizer is large, the polarizer is largely changed in dimension at a high temperature and high humidity so that the resultant display device causes inconveniences such as display unevenness.
The polarizer in which a polyvinyl alcohol-based film dyed with iodine has uniaxially stretched can be produced, for example, by immersing a polyvinyl alcohol into an aqueous solution of iodine to be dyed, and then stretching the resultant film into a length 3 to 7 times the original length of this film. As required, the stretched film may be immersed into an aqueous solution of, for example, boric acid or potassium iodide. Furthermore, before the dyeing, the polyvinyl alcohol-based film may be immersed into water as required to be cleaned with water. The cleaning of the polyvinyl alcohol-based film with water allows to clean stains and a blocking-preventing agent on surfaces of the polyvinyl alcohol-based film, and further produce an advantageous effect of swelling the polyvinyl alcohol-based film to prevent unevenness of the dyeing, and other unevennesses. The stretching may be performed after the dyeing with iodine or while the dyeing is performed. Alternatively, after the stretching, the dyeing with iodine may be performed. The stretching may be performed in an aqueous solution of, for example, boric acid or potassium iodide, or in a water bath.
When a thin polarizer having a thickness of 10 μm or less is used as the polarizer, the active-energy-ray-curable adhesive composition used in the present invention can remarkably produce the advantageous effect thereof (that the resultant adhesive layer satisfies optical endurance in a severe environment at a high temperature and high humidity) The polarizer, the thickens of which is 10 μm or less, is more largely affected by water than any polarizer having a thickness more than 10 μm, so that the former is insufficient in optical endurance in an environment at a high temperature and high humidity to be easily raised in transmittance or lowered in polarization degree. Accordingly, in the case of laminating the polarizer, the thickness of which is 10 μm or less, onto a transparent protective film though an adhesive layer having a bulk water absorption of 10% or less by weight in the invention, the shift of water into the polarizer is restrained in a severely high temperature and high humidity environment. Consequently, the polarizing film can be remarkably restrained from undergoing deteriorations in optical endurances, such as a rise in transmittance and a lowering in polarization degree. The thickness of the polarizer is preferably from 1 to 7 μm from the viewpoint of making the polarizer thinner. Such a thin polarizer is small in thickness unevenness, excellent in perceptibility, and small in dimension change. Furthermore, favorably, this thin polarizer also makes the resultant polarizing film small in thickness.
Typical examples of the thin polarizer include thin polarizing membranes described in JP-A-S51-069644, JP-A-2000-338329, WO 2010/100917 pamphlet, and specifications of PCT/JP2010/001469 and Japanese Patent Applications No. 2010-269002 and No. 2010-26392. These thin polarizing membranes can each be yielded by a producing method including the step of stretching a polyvinyl alcohol-based resin (hereinafter referred to also as a PVA-based resin) and a resin substrate for stretching in a laminate state, and the step of dyeing the laminate. This producing method allows to stretch the laminate, even when the PVA-based resin layer is thin, without causing any inconvenience, such as breaking by the stretching, on the basis of the supporting of the PVA-based resin layer on the resin substrate for stretching.
The thin polarizing membranes are preferably polarizing membranes each yielded by the following producing method, out of producing methods including the step of stretching a PVA-based resin and a substrate in a laminate state and the step of dyeing the stretched laminate, since the laminate can be stretched into a large stretch ratio to improve the resultant in polarizing performance: a producing method including the step of drawing the laminate in an aqueous solution of boric acid, as is described in a pamphlet of WO 2010/100917, PCT/JP 2010/001460, or Japanese Patent Application No. 2010-269002 or 2010-263692 specification. The membranes are in particular preferably membranes each yielded by a producing method including the step of drawing the laminate supplementally in the air before the drawing in the aqueous solution of boric acid, as is described in Japanese Patent Application No. 2010-269002 or 2010-263692 specification.
The material which forms the transparent protective film (2) is preferably a thermoplastic resin excellent in transparency, mechanical strength, thermal stability, water blocking performance, isotropy and others. Examples of the thermoplastic resin 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, and polyvinyl alcohol resins; and mixtures of two or more of these resins. The transparent protective film may contain one or more additives selected appropriately at will. Examples of the additive(s) include an ultraviolet absorbent, an antioxidant, a lubricant, a plasticizer, a release agent, a coloring preventive, a flame retardant, a nucleating agent, an antistatic agent, a pigment and a colorant. The content of the above-mentioned thermoplastic resin in the transparent protective film is preferably from 50 to 100%, more preferably from 50 to 99%, even more preferably from 60 to 98%, in particular preferably from 70 to 97% by weight. If the content of the thermoplastic resin in the transparent protective film is 50% or less by weight, it is feared that the transparent protective film cannot sufficiently express high transparency and other properties which the thermoplastic resin originally has.
The material which forms the transparent protective film (2) is preferably a material excellent in transparency, mechanical strength, heat stability, water blocking performance, isotropy, and others. The humidity permeability of the material is more preferably 150 g/m2/24-hours or less, in particular preferably 140 g/m2/24-hours or less, more preferably 120 g/m2/24-hours or less. In particular, the humidity permeability is gained by a method described in the item EXAMPLES.
In the case of using a transparent protective film having a humidity permeability of 150 g/m2/24-hours or less in the polarizing film, water in the air does not easily enter the inside of the polarizing film, so that the water content by percentage in the polarizing film itself can be restrained from being changed. As a result, the polarizing film can be restrained from being curled or changed in dimension by a storage environment of the film.
A functional layer may be laid onto the surface of the transparent protective film (2) onto which the polarizer (1) is not bonded, this layer being, for example, a hard coat layer, an anti-reflection layer, a sticking-preventing layer, a diffusion layer or an anti-glare layer. The functional layer, which may be a hard coat layer, an anti-reflection layer, a sticking-preventing layer, a diffusion layer or an anti-glare layer, may be fitted to the transparent protective film (2) itself, or may be separately disposed in the form of a member separated from the transparent protective film (2).
The thickness of the transparent protective film (2) may be appropriately determined, and is generally from about 1 to 500 μm, preferably from 1 to 300 μm, more preferably from 5 to 200 μm from the viewpoint of, for example, the strength, the handleability and other workabilities, and the thinness of the film. Furthermore, the thickness is preferably from 10 to 200 μm, preferably from 20 to 80 μm.
The transparent protective films (2) that are laid, respectively, on both surfaces of the polarizer (1) may be transparent protective films made of the same material on the front and rear surfaces of the polarizer, or may be transparent protective films made of, for example, polymeric materials different from each other.
The transparent protective film may be a retardation film having a front retardation of 40 nm or more and/or having a thickness-direction retardation of 80 run or more. Usually, the front retardation and the thickness-direction retardation are controlled into the range of 40 to 200 nm, and that of 80 to 300 nm, respectively. When a retardation film is used as the transparent protective film, this retardation film functions also as a transparent protective film, so that the laminated polarizing film can be made thin.
The retardation film may be, for example, a birefringence film yielded by stretching a polymeric material uniaxially or biaxially, an aligned film of a liquid crystal polymer, or a product in which an aligned layer of a liquid crystal polymer is supported on a film. The thickness of the retardation film is not particularly limited, and is generally from about 20 to 150 μm.
The retardation film may be a reverse wavelength dispersion type retardation film satisfying the following expressions (1) to (3):
0.70<Re[450]/Re[550]<0.97 (1),
1.5×10−3<Δn<6×10−3 (2), and
1.13<NZ<1.50 (3)
wherein Re[450] and Re[550] are, respectively, an in-plane retardation value of the retardation film that is measured at a wavelength of 450 nm at 23° C., and an in-plane retardation value of the retardation film that is measured at a wavelength of 550 nm at 23° C.; Δn is an in-plane birefringence “nx−ny” of the retardation film when the retardation film has a refractive index nx in a slow axis direction of the film, and has a refractive index ny in a fast axis direction of the film; and when the retardation film has a refractive index nz in a thickness direction of the film, NZ is a ratio between “nx−nz”, which is a birefringence of the film in the thickness direction, and “nx−ny”, which is an in-plane birefringence of the film.
The transparent protective film that may be a retardation film is preferably a film having a log Pow of −2 to 2. The log Pow value of the transparent protective film may be calculated out according to a software Chem Draw Ultra manufactured by CambridgeSoft Corp., or the following value may be adopted: a numerical value obtained by bringing monomers having various log Pow values into contact with the retardation film, and making an estimation from the log Pow value of a monomer that invades the film most largely out of the monomers (a specific method therefor is a method of estimating the log Pow value of the film as a numerical value within ±0.5 from the log Pow value of the monomer, which invades the film most largely).
In the laminated polarizing film in each of
<Adhesive Layer (b)>
The adhesive layer (b) is not particularly limited as far as the layer is optically transparent. The layer may be a layer in any one of various forms, such as water-based, solvent-based, hot melt-based, and active-energy-ray-curable forms. As described above, the adhesive layer (b) is preferably a layer having a predetermined thickness and satisfying a predetermined storage modulus.
Examples of the water-based curable adhesive include vinyl polymer-based, gelatin-based, vinyl latex-based, polyurethane-based, isocyanate-based, polyester-based and epoxy-based adhesives. An adhesive layer made of such a water-based adhesive may be formed as, for example, a painted and dried layer of an aqueous solution. When the aqueous solution is prepared, a crosslinking agent, other additives, and a catalyst such as an acid may be blended into the solution as required.
The water-based curable adhesive may be, for example, an adhesive containing a vinyl polymer. The vinyl polymer is preferably polyvinyl alcohol-based resin. The polyvinyl alcohol-based resin is preferably an adhesive containing a polyvinyl alcohol-based resin having an acetoacetyl group from the viewpoint of an improvement of the adhesive in endurance. The crosslinking agent which can be blended into the polyvinyl alcohol-based resin is preferably a compound having at least two functional groups reactive with the polyvinyl alcohol-based resin. Examples of the crosslinking agent include boric acid, borax, carboxylic acid compounds, and alkyldiamines; isocyanates; epoxy compounds; monoaldehydes; dialdehydes; amino-formaldehyde resins; and salts of any divalent metal or trivalent metal, and oxides thereof. A water-soluble silicate may be blended into the polyvinyl alcohol-based resin. Examples of the water-soluble silicate include lithium silicate, sodium silicate, and potassium silicate.
The active-energy-ray-curable adhesive may be an adhesive in any one of various forms. Examples thereof include electron-beam curable adhesives, ultraviolet-curable adhesives, and other active-energy-ray-curable adhesives. The ultraviolet-curable adhesives can be roughly classified into radical polymerization curable adhesives, and cationic polymerization curable adhesives. The radical polymerization curable adhesives may be used as thermosetting resins. As an active-energy-ray-curable adhesive used to form the adhesive layer (b), an active-energy-ray-curable adhesive used to form the adhesive layer (a) is usable.
The adhesive layer (b1) as the adhesive layer (b) is preferably a polyvinyl alcohol adhesive. The adhesive layer (b2) as the adhesive layer (b) is preferably an active-energy-ray-curable adhesive.
The adhesive which forms the adhesive layer (a) or the adhesive layer (b) may appropriately contain an additive if necessary. Examples of the additive include a silane coupling agent, a titanium coupling agents and other coupling agents, adhesion promoters, a typical example thereof being ethylene oxide, additives for improving the adhesive layer in wettability with the transparent film, additives for improving the laminated polarizing film in mechanical strength, workability and others, typical examples thereof including acryloxy group compounds, and hydrocarbon compounds (natural or synthetic resins), ultraviolet absorbers, antiaging agents, dyes, processing aids, ion trapping agents, antioxidants, tackifiers, fillers (other than metal compound filler), plasticizer, leveling agent, antifoaming agent, antistatic agents, and stabilizers such as heat resistant stabilizer and hydrolysis resistant stabilizer.
In the laminated polarizing film of the present invention, the polarizing film (P) and the optical film (3) are bonded to each other through the adhesive layer (a). One or more easily adhesive layers may be laid onto the transparent protective film (2) and/or the optical film (3). Moreover, in the polarizing film (P), one or more easily adhesive layers may be laid onto the polarizer (1) and/or the transparent protective film (2).
The easily adhesive layer or each of the easily adhesive layers may be formed, using a resin that may be of various types, examples of the resin including resins each having a polyester skeleton, a polyether skeleton, a polycarbonate skeleton, a polyurethane skeleton, a silicone-based, a polyamide skeleton, a polyimide skeleton, or a polyvinyl alcohol skeleton. These polymer resins may be used alone or in combination of two or more thereof. In the formation of the easily adhesive layer, a different additive may be added to the layer. Specifically, a tackifier, an ultraviolet absorber, an antioxidant, or a stabilizer such as a heat stabilizer may be used. The thickness of the easily adhesive layer is preferably from 0.01 to 5 μm, more preferably from 0.02 to 2 μm, even more preferably from 0.05 to 1 μm after the layer is dried. Plural easily adhesive layers may be laid. Also in this case, the total thickness of the easily adhesive layers is preferably set into any one of these ranges.
The optical film (3) may be an optical layer that is other than the polarizer (1) and that may be used to form, for example, a liquid crystal display device, such as a retardation film (examples thereof including ½ and ¼ wavelength plates), a viewing angle compensation films, a brightness enhancement film, a reflector or a trans reflector.
Optical films (3) that are two or more layers may be used. When these optical films, which are two or more layers, are used, the same adhesive layer (a) as described above may be used also to laminate the second optical film. The optical film(s) (3) is/are (each) preferably a retardation film.
In the same manner as described above, the retardation film may be a retardation film having a front retardation of 40 nm or more and/or having a thickness-direction retardation of 80 nm or more. Usually, the front retardation and the thickness-direction retardation are controlled into the range of 40 to 200 nm, and that of 80 to 300 nm, respectively.
Examples of the retardation film include a birefringent film yielded by stretching a polymeric material uniaxially or biaxially, an aligned film of a liquid crystal polymer, and a film in which an aligned layer of a liquid crystal polymer is supported on a film. The thickness of the retardation is not particularly limited, and is generally about from 20 to 150 μm.
The retardation film may be a reverse wavelength dispersion type retardation film satisfying the following expressions (1) to (3):
0.70<Re[450]/Re[550]<0.97 (1),
1.5×10−3<Δn<6×10−3 (2), and
1.13<NZ<1.50 (3)
wherein Re[450] and Re[550] are, respectively, an in-plane retardation value of the retardation film that is measured at a wavelength of 450 nm at 23° C., and an in-plane retardation value of the retardation film that is measured at a wavelength of 550 nm at 23° C.; Δn is an in-plane birefringence “nx−ny” of the retardation film when the retardation film has a refractive index nx in a slow axis direction of the film, and has a refractive index ny in a fast axis direction of the film; and when the retardation film has a refractive index nz in a thickness direction of the film, NZ is a ratio between “nx−nz”, which is a birefringence of the film in the thickness direction, and “nx−ny”, which is an in-plane birefringence of the film. The log Pow value of the retardation film is preferably from −2 to 2.
In the laminated polarizing film of the present invention, a pressure-sensitive adhesive layer may be laid for adhering this polarizing film onto a different member such as a liquid crystal cell. A pressure-sensitive adhesive agent which forms the pressure-sensitive adhesive layer is not particularly limited. This agent may be appropriately selected from the following to be used: pressure-sensitive adhesive agents each containing, as a base polymer thereof, acrylic polymer, silicone-based polymer, polyester, polyurethane, polyamide, polyether, fluorine-containing polymer, rubbery polymer, or some other polymers. The pressure-sensitive adhesive agent is in particular preferably an acrylic pressure-sensitive adhesive, or any other pressure-sensitive adhesive that is excellent in optical transparency, and shows adherabilities of appropriate wettability, cohesive property and adhesion to be excellent in weather resistance, heat resistance and others.
Pressure-sensitive adhesive layers different from each other in composition or species may be laid, as superimposed layers, onto a single surface or each surface of the laminated polarizing film or the laminated optical film. When pressure-sensitive adhesive layers are laid, respectively, onto both surfaces of the film, these layers may be different from each other in, for example, composition, species or thickness on the front and rear side of the film. The thickness of (each of) the pressure-sensitive adhesive layer(s) may be appropriately decided in accordance with, for example, the use purpose and adhering strength thereof. The thickness is generally from 1 to 500 μm, preferably from 1 to 200 μm, in particular preferably from 1 to 100 μm.
A separator is temporarily bonded to a naked surface of the pressure-sensitive adhesive layer to cover the surface in order to attain the prevention of the pollution of the surface, and other purposes until the polarizing film is put into practical use. This coverage allows to prevent an object or a person from contacting the pressure-sensitive adhesive layer in the state that the polarizing film is ordinarily handled. The separator may be an appropriate separator according to conventional techniques except the above-mentioned thickness conditions. The separator may be an appropriate flat piece yielded according to the prior art, such as a plastic film, a rubber sheet, a paper, cloth or nonwoven cloth piece, a net, a foamed sheet or a metal foil piece; a laminated body of such flat pieces; or a product in which such a flat piece is optionally subjected to coating treatment with an appropriate release agent, such as a silicone type, long-chain alkyl type or fluorine-containing type agent, or molybdenum sulfide.
The laminated polarizing film or laminated optical film of the present invention is preferably usable to form various devices such as a liquid crystal display device. The formation of the liquid crystal display device may be attained in accordance with the prior art. In other words, any liquid crystal display device is generally formed by fabricating appropriately a liquid crystal cell, a laminated polarizing film or laminated optical film, an optional lighting system, and other constituent parts, and then integrating a driving circuit into the resultant. In the present invention, a method for forming a liquid crystal display device is not particularly limited as far as the laminated polarizing film or laminated optical film according to the invention is used. The method is substantially according to the prior art. A liquid crystal cell therefor may be also of any type, such as a TN type, STN type or π type.
An appropriate liquid crystal display device may be formed, examples of the device including a liquid crystal display device in which a laminated polarizing film or laminated optical film is arranged onto a single side or each of two sides of a liquid crystal cell, and a liquid crystal display device in which a backlight or reflector is used as a lighting system. In this case, the laminated polarizing film or laminated optical film according to the present invention can be set on the single side or each of the two sides of the liquid crystal cell. When laminated polarizing films or laminated optical films of the invention are set up, respectively, on the two sides, these may be the same as or different from each other. When the liquid crystal display device is formed, one or more appropriate components may be further arranged, at one or more appropriate positions of the device, in the form of one or more layers. Examples of the component(s) include a diffusion plate, an anti-glare layer, an anti-reflection film, a protective plate, a prism array, a lens array sheet, a light diffusion plate, and a backlight.
Hereinafter, working examples of the present invention will be described. However, embodiments of the invention are not limited to these examples.
About any adhesive layer or any pressure-sensitive-adhesive layer used in each of the working examples and comparative examples, the glass transition temperature thereof is gained by the following method:
The glass transition temperature is measured, using a viscoelastic spectrometer (trade name: RSA-II) manufactured by Rheometrics, Inc. Conditions for the measurement are as follows: frequency: 1 Hz, sample thickness: 2 mm, compressive load: 100 g, and temperature-raising rate: 5° C./min. In a range from −50 to 200° C., a temperature-dependent spectrum of the tan δ of the layer is measured. A peak temperature thereof is used as a measured value.
Each transparent protective film (2a): corona treatment was applied to each (meth)acrylic resin having a thickness of 50 μm and having a lactone structure. The resultant was used.
Each transparent protective film (2b): corona treatment was applied to each reverse wavelength dispersion type retardation film having a thickness of 55 μm. The resultant was used. The reverse wavelength dispersion type retardation film satisfied the following expressions (1) to (3):
0.70<Re[450]/Re[550]<0.97 (1),
1.5×10−3<Δn<6×10−3 (2), and
1.13<NZ<1.50 (3)
wherein Re[450] and Re[550] are, respectively, an in-plane retardation value of the retardation film that is measured at a wavelength of 450 nm at 23° C., and an in-plane retardation value of the retardation film that is measured at a wavelength of 550 nm at 23° C.; Δn is an in-plane birefringence “nx−ny” of the retardation film when the retardation film has a refractive index nx in a slow axis direction of the film, and has a refractive index ny in a fast axis direction of the film; and when the retardation film has a refractive index nz in a thickness direction of the film, NZ is a ratio between “nx−nz”, which is a birefringence of the film in the thickness direction, and “nx−ny”, which is an in-plane birefringence of the film. The log Pow of the retardation film was 0.1.
To 100 parts of a PVA-based resin containing acetoacetyl (AA) groups (average polymerization degree: 1200, saponification degree: 98.5% by mole, and AA-group modified degree: 5% by mole (the resin is referred to as AA-modified PVA in Table 1) were added 20 parts of methylolmelamine, and the resultant was dissolved into pure water at a temperature of 30° C. to prepare an aqueous solution having a solid concentration adjusted to 0.5%. This was used as an adhesive at a temperature of 30° C.
A polyvinyl alcohol film having an average polymerization degree of 2400, a saponification degree of 99.9% by mole, and a thickness of 75 μm was immersed in hot water of 30° C. temperature for 60 seconds to be swollen. Next, while the film was dyed with an iodine solution that had a temperature of 30° C. and had a concentration of 0.3% by weight (ratio by weight: iodine/potassium iodide=0.5/8) for one minute, the film was stretched 3.5 times. Thereafter, while the film was immersed in an aqueous solution of boric acid that had a temperature of 65° C. and had a concentration of 4% by weight for 0.5 minutes, the film was stretched into a total stretch ratio of 6. After the stretching, the film was dried in an oven of 70° C. temperature for 3 minutes. In this way, each polarizer of 26 μm thickness was yielded.
While the above-mentioned polyvinyl alcohol-based adhesive was painted onto both surface of one of the polarizers, one of the transparent protective films (2a) and one of the transparent protective films (2b) were bonded, respectively, onto both the surfaces. The workpiece was then dried at 50° C. for 5 minutes to produce each polarizing film. The thickness of the adhesive layer (b1) formed on each of the transparent protective films (2a) and (2b) was 0.1 μm. The adhesive layer had a storage modulus of 1.5×104 Pa at 25° C. and had a storage modulus of 1.0×108 Pa at 85° C.
In order to produce each thin polarizing film, a laminate in which a PVA film of 9 μm thickness was formed on an amorphous PET substrate was initially subjected to in-air auxiliary stretching at a stretching temperature of 130° C. to produce a stretched laminate. Next, the stretched laminate was dyed to produce a colored laminate. Furthermore, the colored laminate was subjected to stretching in boric-acid water at a stretching temperature of 65° C. to give a total stretch ratio of 5.94. In this way, each optical film laminate was produced which included a PVA layer of 4 μm thickness that was stretched together with the amorphous PET substrate. This two-stage stretching succeeded in the production of the optical film laminate including the PVA layer of 5 μm thickness, this laminate constituting a highly functional polarizing film in which PVA molecules of the PVA layer formed on the amorphous PET substrate were highly aligned and iodine adsorbed by the dyeing was highly aligned in one direction in the form of a polyiodine ion complex.
While the above-mentioned polyvinyl alcohol-based adhesive was painted onto a surface of the polarizing film of one of the above-mentioned optical film laminates, one of the above-mentioned transparent protective films (2a) was bonded onto the surface. Thereafter, the workpiece was dried at 50° C. for 5 minutes. The thickness of an adhesive layer (b1) formed on the transparent protective film (2a) was 1 μm. The adhesive layer had a storage modulus of 1.5×109 Pa at 25° C., and had a storage modulus of 1.0×108 Pa at 85° C.
Next, the amorphous PET substrate was peeled off, and then an active-energy-ray-curable adhesive described below (this adhesive was the same active-energy-ray-curable adhesive related to an adhesive layer (a) in Example 1, which will be described below) was painted onto the substrate-peeled surface. One of the above-mentioned transparent protective films (2b) was bonded onto the substrate-peeled surface. The adhesive was then cured with ultraviolet rays to produce each thin-polarizing-film-used polarizing film. The polarizing film was represented as (P4)-A. Each polarizing film was produced in the same manner except that instead of the adhesive layer (a) in Example 1, an adhesive layer (a) in Example 3 was used. The polarizing film was represented as (P4)-B. The adhesive (a) formed on the transparent protective film (2a) had a thickness of 5 μm, and had a storage modulus of 8.0×106 Pa at 25° C. and a storage modulus of 8.0×104 Pa at 85° C.
For active energy rays, an ultraviolet ray (gallium sealed metal halide lamp) radiating device Light HAMMER 10 manufactured by Fusion UV Systems, Inc. is used. Bulb: V bulb; peak illuminance: 1600 mW/cm2; and integrated radiation quantity: 1000/mJ/cm2 (at wavelengths of 380 to 440 nm). The illuminance of ultraviolet rays is measured, using a Sola-Check system manufactured by Solatell Ltd.
The viscosity (cp/25° C.) of any active-energy-ray-curable adhesive composition or any pressure-sensitive adhesive used in each of the working examples and the comparative examples is a value measured by an E-type rotary viscometer. The measurement values are shown in Tables 1 to 3.
In each of the examples, in accordance with one of blend tables described as Tables 1 to 3, individual components were blended with each other, and the blend was stirred at 50° C. for one hour to yield an active-energy-ray-curable adhesive. In each of the tables, numerical values about the active-energy-ray-curable adhesive show, respectively, parts by weight of the individual components when the total amount of the radical polymerizable compounds in this adhesive was regarded as 100 parts by weight.
Each liquid crystal type retardation film was used (i.e., each film in which a liquid crystal aligned film of 4 μm thickness was supported on a polyethylene terephthalate film of 38 μm thickness). The log Pow of the retardation film was 0.5.
In each of the examples, corona treatment was applied to each of some of the above-mentioned liquid crystal type retardation films. An active-energy-ray-curable adhesive composition related to the adhesive layer (a) shown in Table 1 was painted onto the corona-treated surface to give a thickness shown in Table 1, using an MCD coater (manufactured by Fuji Machinery Co., Ltd.) (cell shape: honeycomb, the number of gravure roll lines: 1000/inch, and rotating speed: 140% of line speed).
The adhesive applied surface of each of a half of the corona-treated retardation films, in the example, was bonded onto the transparent protective film (2b) side of one of the polarizing films (P1), as well as the adhesive applied surface of each of the remaining half was bonded onto the transparent protective film (2b) side of one of the polarizing films (P4). Thereafter, the above-mentioned ultraviolet rays were radiated to the former resultant workpieces, as well as the latter workpieces, after predetermined periods (15 seconds, 21 seconds, and 42 seconds) elapsed, respectively, to cure the active-energy-ray-curable adhesive composition related to their adhesive layers (a). In this way, laminated polarizing films were yielded in each of the examples. In each of Examples 1 to 13, and Comparative Examples 1 to 5, the above-mentioned (P4)-A was used as the polarizing film (P4). In Example 14, the above-mentioned (P4)-B was used as the polarizing film (P4).
Evaluations described below were made about the active-energy-ray-curable adhesive, and the laminated polarizing films yielded in each of the examples. The results are shown in Table 1 to 3.
The polyethylene terephthalate film on the liquid crystal type retardation film side of each of films to be used in this test, out of the laminated polarizing films, was peeled off, and a polybutyl acrylate-based pressure-sensitive adhesive (thickness: 23 μm) was bonded onto the film-peeled surface. Furthermore, the resultant was cut into a size of 200 mm in parallel with the stretched direction of the polarizer and 15 mm in a direction orthogonal thereto. A utility knife was used to make a cut into between the polarizing film and the retardation film, and then the release film of the polybutyl acrylate-based pressure-sensitive adhesive was peeled off. The adhesive surface was bonded to a glass plate. A machine Tensilon was used to peel the polarizing film and the retardation film from each other into 120-degree directions at a peel rate of 10000 mm/min. The peel strength (N/15-mm) thereof was measured.
The polyethylene terephthalate film on the liquid crystal type retardation film side of each of films to be used in this test, out of the laminated polarizing films, was peeled off, and a polybutyl acrylate-based pressure-sensitive adhesive (thickness: 23 μm) was bonded onto the film-peeled surface. Furthermore, the resultant was cut into a size of 300 mm in parallel with the stretched direction of the polarizer and 200 mm in a direction orthogonal thereto. The release film of the polybutyl acrylate-based pressure-sensitive adhesive was peeled off. The adhesive surface was bonded to a glass plate. This sample was pressurized in an environment of 50° C. and 5 atm. for 15 minutes, and put in an environment of 85° C. for 500 hours. Thereafter, in any end of the polarizing film, the peel distance of the film was measured. When no peel was generated, the sample was judged to be good (circular mark); when a peel was generated in the range of a distance of 2 mm or less from the end, the sample was judged to be fair (triangular mark); or when a peel giving a peel distance more than 2 mm, the sample was judged to be bad (cross mark).
The adhesive liquid was put into a glass bottle of 250 mL volume, and the bottle was allowed to stand still in an opening system in an environment of 25° C. temperature and 50% relative humidity while the liquid was stirred with a magnetic stirrer. Thereafter, it was visually evaluated whether or not the adhesive liquid underwent phase separation to become clouded. When the sample was transparent without becoming clouded over a stirring period of 24 hours, the sample was judged to be good; the sample was transparent without becoming clouded over a stirring period of 12 hours but became clouded in a stirring period of 24 hours, the sample was judged to be fair; or when the sample became clouded in a stirring period of 12 hours, the sample was judged to be bad.
A pressure-sensitive-adhesive layer was laminated onto the retardation film surface of each of films to be used in this test, out of the laminated polarizing films. The resultant was cut into a rectangle of a size of 50 mm in the stretched direction of the polarizer and 100 mm in a direction perpendicular thereto. This laminated polarizing film was laminated onto a glass plate having a thickness of 0.5 mm, a length of 120 mm, and a width of 60 mm to produce each sample. In order to prevent the glass plate from being broken, a cellophane tape had been bonded to the whole of the rear surface of the glass plate.
The produced sample was dropped from a height of 1 μm. The drop was repeated 100 times. A peel state of any end of the polarizing film was then visually observed.
◯: no peel was observed.
Δ: the distance of a peel from the end was less than 1 mm.
x: the distance of a peel from the end was 1 mm or more.
A pressure-sensitive-adhesive layer was laminated onto the retardation film surface of each of films to be used in this test, out of the laminated polarizing films. The resultant was cut into a rectangle of a size of 200 mm in the stretched direction of the polarizer and 400 mm in a direction perpendicular thereto. Through the pressure-sensitive-adhesive layer, the laminated polarizing film was laminated onto each of both surfaces of a liquid crystal cell (taken from “32-inch liquid crystal television BRAVIA (registered trade name) KDL-32F1” manufactured by Sony Corp.) into a crossed Nichol state to produce a liquid crystal panel. About this liquid crystal panel, the following tests were made:
1: heating test (at 85° C. for 12 hours), and
2: heat cycle test from −40 to 85° C.; 100 cycles.
After the tests, the liquid crystal panel was visually observed, and streak unevenness therein was evaluated in the following criterion:
◯: the generation of streak unevenness was not observed.
Δ: the generation of slight streak unevenness was observed in only an end of the panel.
x: streak unevenness was generated.
In Tables 1 to 3, radical polymerizable compounds are as follows:
(A) Components A having a log Pow of −2 to 2:
HEAA: hydroxyethylacrylamide, manufactured by Kohjin Co., Ltd., log Pow=−0.56;
ACMO: acryloylmorpholine, manufactured by Kohjin Co., Ltd., log Pow=0.20;
NVP: (N-vinyl-2-pyrrolidone, manufactured by Nippon Shokubai Co., Ltd., log Pow=−0.24); and
DEAA: (N,N-diethylacrylamide), log Pow=1.69)
(B) Component B Having a Log Pow More than 7:
ISTA: isostearyl acrylate, manufactured by Osaka Organic Chemical Industry Ltd., log Pow=7.5.
LIGHT ACRYLATE L-A: lauryl acrylate, manufactured by Kyoei Kyoeisha Chemical Co., Ltd., log Pow=6.0.
4HBA: 4-hydroxybutyl acrylate, manufactured by Osaka Organic Chemical Industry Ltd., log Pow=0.68; and
PLACCEL FA1DDM: one-mole-caprolactone added product of 2HEA, manufactured by Daicel Corp., log Pow=1.06.
TPGDA: tripropylene glycol diacrylate, manufactured by Toagosei Co., Ltd., log Pow=1.68;
LIGHT ACRYLATE 9EG-A: ethylene glycol (average value of added mole numbers: 9) diacrylate, manufactured by Kyoeisha Chemical Co., Ltd., log Pow=−0.1; and
LIGHT ACRYLATE 1,9NDA: 1,9-nonanediol diacrylate, manufactured by Kyoeisha Chemical Co., Ltd., log Pow=3.68.
AAEM: 2-acetoacetoxyethyl methacrylate, manufactured by the Nippon Synthetic Chemical Industry Co., Ltd.
UP-1190 (ARUFON UP-1190), manufactured by Toagosei Co., Ltd.
KAYACURE DETX-S: diethylthioxanthone, manufactured by Nippon Kayaku Co., Ltd.
Photopolymerization initiator:
IRGACURE 907 (compound represented by the general formula (2)): 2-methyl--(4-methylthiophenyl)-2-morpholinopropane-1-one, manufactured by the BASF;
Crosslinking Agent:
CORONATE L: (Adduct of trimethylolpropane and tolylene diisocyanate, manufactured by Nippon Polyurethane Industry Co., Ltd.); and
| Number | Date | Country | Kind |
|---|---|---|---|
| 2016-084754 | Apr 2016 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2017/008736 | 3/6/2017 | WO | 00 |
