JP4836246B2 - Method for producing adhesive optical film, adhesive optical film, and image display device - Google Patents

Description

  The present invention relates to a method for producing an adhesive optical film having an adhesive layer on at least one surface of an optical film. The present invention also relates to an adhesive optical film obtained by the above production method, and further to an image display device such as a liquid crystal display device or an organic EL display device using the same. Examples of the optical film include a polarizing plate, a retardation plate, an optical compensation film, a brightness enhancement film, and a laminate of these.

  In a liquid crystal display or the like, it is indispensable to dispose polarizing elements on both sides of a liquid crystal cell because of its image forming method, and generally a polarizing plate is attached. In addition to polarizing plates, various optical elements have been used for liquid crystal panels in order to improve the display quality of displays. For example, a retardation plate for preventing coloring, a viewing angle widening film for improving the viewing angle of a liquid crystal display, and a brightness enhancement film for increasing the contrast of the display are used. These films are collectively called optical films.

  When sticking the optical film on a liquid crystal cell, an adhesive is usually used. In addition, the adhesion between the optical film and the liquid crystal cell, or the optical film is usually in close contact with each other using an adhesive in order to reduce the loss of light. In such a case, since the adhesive has the merit that a drying step is not required for fixing the optical film, the adhesive is an adhesive optical film provided in advance as an adhesive layer on one side of the optical film. Generally used (Patent Document 1, Patent Document 2).

  As a method for producing an adhesive type optical film, a method of applying an adhesive solution to an optical film, drying in a drying oven or the like to form an adhesive layer, or applying an adhesive solution to a release film, A method is employed in which an adhesive layer formed by drying in a drying oven or the like is transferred to an optical film. Among the above methods, the latter transfer method is preferable because the pressure-sensitive adhesive layer is formed in advance, and therefore, when the pressure-sensitive adhesive layer is formed, heat resistance, solvent resistance, and the like are not required for the optical film. In the production process of the pressure-sensitive adhesive optical film, in the pressure-sensitive adhesive layer, the solvent component in the coated pressure-sensitive adhesive solution evaporates in a drying process such as an air-drying zone and a drying oven immediately after coating to the drying process. Is formed.

However, depending on the manufacturing conditions such as the atmospheric environment, the type of the pressure-sensitive adhesive solution, and the coating speed in the method for manufacturing the pressure-sensitive adhesive optical film, the appearance of the pressure-sensitive adhesive layer becomes cloudy, the haze increases, There was a case where a defect occurred at the interface between the optical film and the pressure-sensitive adhesive layer later.
Japanese Patent Laid-Open No. 2003-73639 JP 2002-250814 A

  The present invention has been made in view of such circumstances, and an object of the present invention is to provide a method for producing a pressure-sensitive adhesive optical film that has good anchoring properties between the optical film and the pressure-sensitive adhesive layer and has no appearance defects. To do.

  Another object of the present invention is to provide an adhesive optical film obtained by the production method, and further to provide an image display device using the adhesive optical film.

  As a result of intensive studies to solve the above problems, the present inventors have found the following method for producing an adhesive optical film and have completed the present invention.

That is, in the present invention, at least one surface of the base film is coated with a pressure-sensitive adhesive solution containing a pressure-sensitive adhesive and a solvent (1), and the pressure-sensitive adhesive solution is subjected to a drying treatment to remove the pressure-sensitive adhesive layer by solvent removal. In the method for producing a pressure-sensitive adhesive optical film having a pressure-sensitive adhesive layer on at least one surface of the optical film, including the step (2) of forming,
The temperature of the base film until the drying step (2) is applied to the base film after the coating step (1) is performed so that condensation does not occur in the adhesive solution applied to the base film. The haze of the pressure-sensitive adhesive layer formed after the drying step (2) is controlled to a temperature not lower than the dew point in the atmospheric environment where the water is placed and not higher than the boiling point of the solvent in the pressure-sensitive adhesive solution. The present invention relates to a method for producing a pressure-sensitive adhesive optical film, which is 0.3% or less .

  In the method for producing an adhesive optical film, when the base film is a release film, the release film was formed on the release film after being subjected to the coating step (1) and the drying step (2). A step (3) of transferring the formed pressure-sensitive adhesive layer to the optical film can be further included.

  In the production method of the pressure-sensitive adhesive optical film, when the substrate film is an optical film, the coating step (1) can be performed on the optical film.

  In the production method of the pressure-sensitive adhesive optical film, the temperature control of the base film is suitably performed by providing a heating roll after the coating step (1) and before the drying step (2). be able to. In this case, the temperature of the heating roll is preferably set such that the temperature of the base film that has passed through the heating roll is higher than the ambient environmental temperature by at least 5 ° C.

  The method for producing the pressure-sensitive adhesive optical film can be suitably applied to the case where an adhesive containing a base polymer and a crosslinking agent is used. In particular, the present invention can be suitably applied when an acrylic polymer is used as the base polymer.

  The method for producing the pressure-sensitive adhesive optical film can be suitably applied when the crosslinking agent is a compound having reactivity with water. As a compound having reactivity with water, for example, an isocyanate compound (isocyanate-based crosslinking agent) can be exemplified, and the present invention can be suitably applied in the case of the compound.

  Moreover, this invention relates to the adhesive optical film obtained by the said manufacturing method. The present invention also relates to an image display apparatus using at least one of the adhesive optical films. The pressure-sensitive adhesive optical film of the present invention is used in combination of one or more sheets depending on various usage modes of an image display device such as a liquid crystal display device.

  In the production method of the pressure-sensitive adhesive optical film of the present invention, depending on the production environment such as the atmospheric environment of the production method, the type of the pressure-sensitive adhesive solution, the coating speed, the appearance defect of the pressure-sensitive adhesive layer, the optical film and the pressure-sensitive adhesive layer, Therefore, the atmospheric environment of the manufacturing method was examined. As a result, the inventors have found that the above problems occur due to the following causes, and found the present invention.

  From the application step (1) of the pressure-sensitive adhesive solution to the end of the drying step (2), the solvent component in the pressure-sensitive adhesive solution (coating film) applied to the base film evaporates, and by the latent heat of evaporation, The temperature of the coating film decreases. At that time, when the temperature of the coating film is equal to or lower than the dew point in the atmospheric environment (temperature, humidity) of the air to which the coating film is exposed, an air-drying zone in a process between the coating process (1) and the drying process (2). Further, in the drying step (2), it was found that condensation occurred on the coating film, and that the above problem was caused by the condensation. That is, when condensation occurs on the coating film, the surface of the coating film that has not been completely dried is roughened, or the adhesive component dissolved in the solvent is deposited, causing problems of white turbidity and haze increase. it is conceivable that.

  Therefore, in the present invention, in the air drying zone between the coating step (1) and the drying step (2), the temperature of the base film is set to an atmospheric environment in which the base film is placed so that no condensation occurs. The problem is solved by controlling the temperature below the dew point below and below the boiling point of the solvent in the adhesive solution to prevent the occurrence of condensation on the coating film.

  As described above, the method for producing a pressure-sensitive adhesive optical film of the present invention prevents condensation that occurs in the coating film in the air-drying zone. Therefore, the production method of the present invention can be suitably applied in an air-drying zone atmosphere environment particularly in a high temperature and high humidity environment. Condensation occurs remarkably when the coating speed of the pressure-sensitive adhesive solution increases or the air volume during drying increases. Even in such a case, according to the present invention, condensation can be prevented. .

  In addition, as a method for producing an adhesive optical film, when an adhesive optical film is produced by a so-called transfer method in which an adhesive layer formed on a release film is transferred to an optical film, Condensation that occurs affects the drop in anchoring properties of the adhesive layer. Therefore, the production method of the pressure-sensitive adhesive optical film of the present invention is suitable for application of a so-called transfer method.

  Further, the dew condensation generated on the coating film is caused when the pressure-sensitive adhesive contains a crosslinking agent, particularly when a compound reactive with water (such as an isocyanate-based crosslinking agent) is used as the crosslinking agent. The surface of the coating film and the resulting pressure-sensitive adhesive layer is roughened by the reaction between the cross-linking agent present in the film and condensation (water). In particular, in the case of the transfer method, the influence of the coating film surface on the anchoring property with the optical film is large. Therefore, the pressure-sensitive adhesive optical film of the present invention is suitable when a crosslinking agent is contained, particularly when a compound having reactivity with water is used as the crosslinking agent.

  Moreover, the dew condensation which arises in the said coating film tends to arise when the boiling point of the solvent component in an adhesive solution is low. On the other hand, in the case where the condensation occurring in the coating film has a low saturated solubility with water as the solvent component in the pressure-sensitive adhesive solution, a problem occurs remarkably. That is, in a coating film containing a solvent having low saturation solubility with water, dew condensation (water) generated on the coating film surface remains on the surface. When a compound having reactivity with water is present on the surface of the coating film, it is presumed that the problem becomes remarkable due to the rough surface of the coating film and the resulting pressure-sensitive adhesive layer. Even when such a solvent is used, according to the production method of the present invention, condensation can be prevented.

  Below, the manufacturing method of the adhesive optical film of this invention is demonstrated. In the present invention, the pressure-sensitive adhesive solution coating step (1) is applied to at least one surface of the base film, and then the temperature of the base film is controlled to a temperature range in which condensation does not occur, and then the drying step (2 ) To form an adhesive layer. In addition, when using an optical film as a base film, a coating process (1) is given with respect to an optical film, and an adhesive layer is formed through a drying process (2). A release film can be bonded to the pressure-sensitive adhesive layer formed here. On the other hand, when a release film is used as the substrate film, the release film is subjected to a coating step (1), and a pressure-sensitive adhesive layer is formed through a drying step (2). Then, it is transferred onto the optical film by the step (3) of transferring to the optical film.

  The coating method of the adhesive solution on the base film in the coating step (1) is not particularly limited, and a normal method can be adopted. Examples thereof include a slot die method, a reverse gravure coating method, a micro gravure method, a dip method, a spin coating method, a brush coating method, a roll coating method, and a flexographic printing method.

The amount of the pressure-sensitive adhesive solution applied on the base film is preferably in the range of about 50 to 500 g / m ² based on the amount of the solution. Moreover, it is preferable to apply an adhesive solution so that the thickness of the adhesive layer after drying may be 3-50 micrometers, Furthermore, 10-30 micrometers.

  The temperature control of the base film is performed so that condensation does not occur between the coating step (1) and the drying step (2), that is, in the air drying zone of the adhesive solution (coating film) on the base film. In addition, the temperature of the substrate film is controlled by controlling the temperature to be not lower than the dew point in the atmosphere environment where the substrate film is placed and not higher than the boiling point of the solvent in the adhesive solution. It is not necessary to control the temperature of the base film in the entire air-drying zone, and it may be performed after the possibility of condensation. In this way, before the risk of condensation occurs, by setting the temperature of the base film to be equal to or higher than the condensation point, it is possible to prevent the occurrence of condensation on the air drying zone and further on the coating film in the drying process. The dew point temperature is the temperature at which the saturated vapor pressure is reached from the temperature and humidity of the atmospheric environment in the air-drying zone from the saturated vapor pressure curve of water. The boiling point of the solvent in the adhesive solution is also the boiling point in the atmospheric environment (temperature, humidity) in the air drying zone. When the solvent is a mixed solvent, it is the boiling point of the mixed solvent. When the temperature of the substrate film exceeds the boiling point of the solvent, problems such as foaming are likely to occur due to rapid evaporation of the solvent.

  The production method of the present invention is intended to prevent the occurrence of condensation in the air-drying zone, and is therefore useful when the atmospheric environment in the air-drying zone tends to cause condensation. For example, when the temperature is 15 to 40 ° C., particularly 20 to 40 ° C. and the relative humidity is 60 to 90%, particularly 70 to 90%, the production method of the present invention can be suitably applied.

  In the air-drying zone, as a means for controlling the temperature of the base film within the above range, for example, a heating roll is installed and heated from the base film side, thereby controlling the coating film temperature to the dew point or higher. There are methods. In addition, a heating zone (heating tank, etc.) is provided in the air-drying zone to control the temperature of the base film within the above range, and the coating solution temperature (base material) is applied after pre-heating the adhesive solution. And a method of controlling the film temperature) above the dew point. These methods can be used in combination. In order to suppress the prevention of dew condensation, the moisture in the atmospheric environment is removed (dehumidified) to reduce the dew point temperature, the solvent composition of the adhesive solution is changed, and the coating film temperature is suddenly lowered. Although there are methods for preventing the above, these methods can be employed in addition to the method of the present invention (a method for controlling the temperature of the base film).

  In addition, it is preferable to control the temperature of the base film at a temperature that is usually higher than the ambient temperature by at least 5 ° C. Furthermore, it is preferably 7 ° C. or higher. Moreover, it is preferable to set the temperature of the said base film to the temperature higher 10 degreeC or more than a dew point. Moreover, the upper limit of the temperature of a base film is 100 degrees C or less, Furthermore, 90 degrees C or less is preferable. Such a temperature setting is, when a compound having reactivity with water, such as an isocyanate compound, is used as a crosslinking agent in the pressure-sensitive adhesive, so that the deterioration of the compound can be suppressed, and foaming accompanying rapid evaporation of the solvent, etc. Good results are obtained in reducing the appearance defects.

  In the drying step (2), drying conditions are appropriately set according to the type of the pressure-sensitive adhesive solution applied to the base film, the thickness of the pressure-sensitive adhesive layer, the conveyance speed of the film, and the like. The drying conditions are usually about 50 to 120 ° C., and further heat treatment at 60 to 110 ° C. to volatilize the solvent. The heat treatment time can be usually about 10 to 90 seconds, and further about 30 to 80 seconds. The heat treatment means is not particularly limited. For example, a method such as a hot plate, an oven, or a belt furnace is appropriately employed. In addition, after the coating process (1), the time until the drying process (2) is completed is such that heat is efficiently applied to the pressure-sensitive adhesive solution (coating film) on the base film with a heating roll or a drying oven. It is preferable to evaporate the solvent from the pressure-sensitive adhesive solution over a period of at least 10 seconds in order to transmit to the surface and to maintain the uniformity of the dry surface.

  In FIG. 1, the manufacturing method of the adhesive type optical film which uses the release film 1 as a base film and forms the adhesive layer 2 with the adhesive solution 21 on the single side | surface is shown. In FIG. 1, the pressure-sensitive adhesive solution 2 is applied to the release film 1 running continuously by the die coater 11 as a coating step (1). Next, in order to control the temperature of the base film, the drying process (2) is performed by the drying oven 12 after passing through the heating roll 13. The pressure-sensitive adhesive layer 2 formed in the drying step (2) is transferred to the optical film 3 by the pair of transfer rolls 14 as the transfer step (3), and the pressure-sensitive adhesive optical film A is manufactured. In FIG. 1, when an optical film is used as the substrate film, the transfer step (3) is not particularly required.

  In FIG. 1, the setting position of the heating roll 13 is provided so that condensation does not occur in the adhesive solution (coating film) 21 applied on the base film 1. A plurality of heating rolls can be provided. The length from the coating process (1) to the drying process (2) is usually about 0.5 to 10 m, more preferably 1 to 8 m, and the conveying speed is about 0.5 to 50 m / min, and further 1 to 40 m. / Min. The installation position of the heating roll 13 is determined by the atmosphere environment in the air-drying zone, the length from the coating process (1) to the drying process (2), the conveyance speed, and the like. The installation position of the heating roll 13 is usually preferably around the midpoint of the length from the coating process (1) to the drying process (2).

  Moreover, what is used conventionally can be used as an adhesive solution used for this invention. The pressure-sensitive adhesive is not particularly limited, and for example, an acrylic polymer, silicone polymer, polyester, polyurethane, polyamide, polyether, fluorine-based or rubber-based polymer is appropriately selected and used. Can do. As the pressure-sensitive adhesive, those containing the base polymer and the crosslinking agent are preferably used. In particular, those excellent in optical transparency, exhibiting appropriate wettability, cohesiveness, and adhesive pressure-sensitive adhesive properties and excellent in weather resistance, heat resistance, etc. are preferably used. As such a characteristic, an acrylic pressure-sensitive adhesive having an acrylic polymer as a base polymer is preferably used.

  The acrylic pressure-sensitive adhesive has an acrylic polymer having a main skeleton of an alkyl (meth) acrylate monomer unit as a base polymer. (Meth) acrylate refers to acrylate and / or methacrylate, and (meth) of the present invention has the same meaning. The average carbon number of the alkyl group of the alkyl (meth) acrylate constituting the main skeleton of the acrylic polymer is about 1 to 12, and specific examples of the alkyl (meth) acrylate include methyl (meth) acrylate, ethyl (Meth) acrylate, n-butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, isooctyl (meth) acrylate, isononyl (meth) acrylate, lauryl (meth) acrylate, etc. can be exemplified, and these are used alone or in combination. it can. Among these, alkyl (meth) acrylates having 1 to 9 carbon atoms in the alkyl group are preferable.

  In the acrylic polymer, one or more kinds of various monomers are introduced by copolymerization for the purpose of improving adhesiveness and heat resistance. Specific examples of such copolymerization monomers include, for example, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, (meth) acrylic acid 6 Hydroxyl group-containing monomers such as hydroxyhexyl, 8-hydroxyoctyl (meth) acrylate, 10-hydroxydecyl (meth) acrylate, 12-hydroxylauryl (meth) acrylate and (4-hydroxymethylcyclohexyl) -methyl acrylate Carboxyl group-containing monomers such as (meth) acrylic acid, carboxyethyl (meth) acrylate, carboxypentyl (meth) acrylate, itaconic acid, maleic acid, fumaric acid and crotonic acid; acid anhydrides such as maleic anhydride and itaconic anhydride Monomer-containing monomer; Caprolac of acrylic acid Adducts such as styrene sulfonic acid, allyl sulfonic acid, 2- (meth) acrylamide-2-methylpropane sulfonic acid, (meth) acrylamide propane sulfonic acid, sulfopropyl (meth) acrylate, (meth) acryloyloxynaphthalene sulfonic acid, etc. And sulfonic acid group-containing monomers such as 2-hydroxyethyl acryloyl phosphate.

  Moreover, a nitrogen-containing vinyl monomer is mention | raise | lifted. For example, maleimide, N-cyclohexylmaleimide, N-phenylmaleimide; N-acryloylmorpholine; (meth) acrylamide, N, N-dimethyl (meth) acrylamide, N, N-diethyl (meth) acrylamide, N-hexyl ( (N-substituted) such as (meth) acrylamide, N-methyl (meth) acrylamide, N-butyl (meth) acrylamide, N-butyl (meth) acrylamide, N-methylol (meth) acrylamide, and N-methylolpropane (meth) acrylamide ) Amide monomer; aminoethyl (meth) acrylate, aminopropyl (meth) acrylate, N, N-dimethylaminoethyl (meth) acrylate, t-butylaminoethyl (meth) acrylate, 3- (3- Pyridinyl) propyl (meth) acrelane (Meth) acrylic acid alkylaminoalkyl monomers such as (meth) acrylic acid methoxyethyl, (meth) acrylic acid alkoxyalkyl monomers such as ethoxyethyl; N- (meth) acryloyloxymethylene succinimide, Succinimide monomers such as N- (meth) acryloyl-6-oxyhexamethylene succinimide, N- (meth) acryloyl-8-oxyoctamethylene succinimide, N-acryloylmorpholine, and the like are also examples of monomers for modification.

  Further, vinyl acetate, vinyl propionate, N-vinyl pyrrolidone, methyl vinyl pyrrolidone, vinyl pyridine, vinyl piperidone, vinyl pyrimidine, vinyl piperazine, vinyl pyrazine, vinyl pyrrole, vinyl imidazole, vinyl oxazole, vinyl morpholine, N-vinyl carboxylic acid amide , Vinyl monomers such as styrene, α-methylstyrene, N-vinylcaprolactam; cyanoacrylate monomers such as acrylonitrile and methacrylonitrile; epoxy group-containing acrylic monomers such as glycidyl (meth) acrylate; (meth) acrylic Polyethylene glycol acid, polypropylene glycol (meth) acrylate, methoxyethylene glycol (meth) acrylate, methoxypolypropylene (meth) acrylate Glycol acrylic ester monomers such as recall; (meth) acrylic acid tetrahydrofurfuryl, fluorine (meth) acrylate, silicone (meth) acrylate and acrylic acid ester monomers such as 2-methoxyethyl acrylate, etc. may also be used.

  Among these, carboxyl group-containing monomers such as acrylic acid are preferably used from the viewpoints of adhesion to liquid crystal cells and adhesion durability for optical film applications.

  Although the ratio of the copolymerization monomer in the acrylic polymer is not particularly limited, it is preferably about 0.1 to 10% in weight ratio.

  The average molecular weight of the acrylic polymer is not particularly limited, but the weight average molecular weight is preferably about 300,000 to 2.5 million. The acrylic polymer can be produced by various known methods. For example, a radical polymerization method such as a bulk polymerization method, a solution polymerization method, or a suspension polymerization method can be appropriately selected. As the radical polymerization initiator, various known azo and peroxide initiators can be used. The reaction temperature is usually about 50 to 80 ° C., and the reaction time is 1 to 8 hours. Among the above production methods, the solution polymerization method is preferable, and ethyl acetate, toluene and the like are generally used as the solvent for the acrylic polymer. The solution concentration is usually about 20 to 80% by weight.

  Examples of the base polymer of the rubber adhesive include natural rubber, isoprene rubber, styrene-butadiene rubber, recycled rubber, polyisobutylene rubber, styrene-isoprene-styrene rubber, and styrene-butadiene-styrene rubber. Etc. Examples of the base polymer of the silicone-based pressure-sensitive adhesive include dimethylpolysiloxane and diphenylpolysiloxane, and those base polymers into which a functional group such as a carboxyl group is introduced can also be used.

  The pressure-sensitive adhesive is preferably a pressure-sensitive adhesive composition containing a crosslinking agent. Examples of the polyfunctional compound that can be blended in the pressure-sensitive adhesive include organic crosslinking agents and polyfunctional metal chelates. Examples of the organic crosslinking agent include an epoxy crosslinking agent, an isocyanate crosslinking agent, and an imine crosslinking agent. As the organic crosslinking agent, an isocyanate crosslinking agent is preferable. A polyfunctional metal chelate is one in which a polyvalent metal is covalently or coordinately bonded to an organic compound. Examples of polyvalent metal atoms include Al, Cr, Zr, Co, Cu, Fe, Ni, V, Zn, In, Ca, Mg, Mn, Y, Ce, Sr, Ba, Mo, La, Sn, Ti, and the like. can give. Examples of the atom in the organic compound that is covalently or coordinately bonded include an oxygen atom, and the organic compound includes an alkyl ester, an alcohol compound, a carboxylic acid compound, an ether compound, a ketone compound, and the like.

  Among these crosslinking agents, isocyanate-based crosslinking agents are preferable from the viewpoints of adhesive properties, anchoring properties to optical films, cohesiveness of the pressure-sensitive adhesive layer, and the like. Isocyanate crosslinking agents include diisocyanates such as tolylene diisocyanate, diphenylmethane diisocyanate, xylylene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, diisocyanate adducts modified with various polyols such as trimethylolpropane, isocyanurate rings and burettes. Examples thereof include polyisocyanate compounds in which bodies and allophanate bodies are formed.

  The blending ratio of the base polymer such as the acrylic polymer and the crosslinking agent is not particularly limited, but usually about 0.01 to 6 parts by weight of the crosslinking agent (solid content) is preferable with respect to 100 parts by weight of the base polymer (solid content). Furthermore, about 0.1-3 weight part is preferable.

  Furthermore, the pressure-sensitive adhesive may include a tackifier, a plasticizer, glass fiber, glass beads, metal powder, other inorganic powders, a pigment, a colorant, a filler, an antioxidant, if necessary. Various additives may be used as appropriate, such as an agent, an ultraviolet absorber, a silane coupling agent, and the like without departing from the object of the present invention. Moreover, it is good also as an adhesive layer etc. which contain microparticles | fine-particles and show light diffusibility.

  Moreover, as a solvent component used for the said adhesive solution, various solvents can be used according to a base polymer. Examples of the solvent include aromatic hydrocarbon solvents such as toluene and xylene; aliphatic solvents such as hexane, heptane and pentane; ketone solvents such as methyl ethyl ketone and methyl isobutyl ketone. Among these, toluene, ethyl acetate, or a mixture thereof is useful in terms of solubility in the base polymer, coating property during coating, and drying properties. In particular, the present invention is suitable when a solvent having low solubility with water, such as toluene or ethyl acetate, is used as the solvent. These solvents have low solubility in water, and when condensation occurs, they remain on the surface of the adhesive solution (coating film), react with the cross-linking agent on the coating film surface, and are prone to malfunctions. A water layer is formed on the surface of the previous coating film, which tends to cause an appearance defect. In the present invention, even when such a solvent is used, the occurrence of the above-mentioned problem that can prevent dew condensation can be suppressed.

  In the pressure-sensitive adhesive solution, the concentration of the base polymer in the solution is set in terms of coating properties, drying properties, appearance, etc., but is usually about 3 to 20% by weight, preferably 7 to 15% by weight. is there.

  Constituent materials for the release film include paper, polyethylene, polypropylene, synthetic resin films such as polyethylene terephthalate, rubber sheets, paper, cloth, non-woven fabrics, nets, foam sheets and metal foils, and suitable thin leaves such as laminates thereof. Etc. In order to improve the peelability from the pressure-sensitive adhesive layer, the surface of the release sheet may be subjected to a low-adhesive release treatment such as silicone treatment, long-chain alkyl treatment, and fluorine treatment as necessary.

  As an optical film, what is used for formation of image display apparatuses, such as a liquid crystal display device, is used, and the kind in particular is not restrict | limited. For example, the optical film includes a polarizing plate. A polarizing plate having a transparent protective film on one or both sides of a polarizer is generally used.

  The polarizer is not particularly limited, and various types can be used. Examples of polarizers include dichroic iodine and dichroic dyes on hydrophilic polymer films such as polyvinyl alcohol films, partially formalized polyvinyl alcohol films, and ethylene / vinyl acetate copolymer partially saponified films. Examples thereof include polyene-based oriented films such as those obtained by adsorbing substances and uniaxially stretched, polyvinyl alcohol dehydrated products and polyvinyl chloride dehydrochlorinated products. Among these, a polarizer composed of a polyvinyl alcohol film and a dichroic material such as iodine is preferable. The thickness of these polarizers is not particularly limited, but is generally about 5 to 80 μm.

  A polarizer obtained by dyeing a polyvinyl alcohol film with iodine and uniaxially stretching it can be prepared by, for example, dying polyvinyl alcohol in an aqueous solution of iodine and stretching it 3 to 7 times the original length. If necessary, it can be immersed in an aqueous solution such as potassium iodide which may contain boric acid, zinc sulfate, zinc chloride or the like. Further, if necessary, the polyvinyl alcohol film may be immersed in water and washed before dyeing. In addition to washing the polyvinyl alcohol film surface with dirt and anti-blocking agents by washing the polyvinyl alcohol film with water, it also has the effect of preventing unevenness such as uneven coloring by swelling the polyvinyl alcohol film. is there. Stretching may be performed after dyeing with iodine, may be performed while dyeing, or may be dyed with iodine after stretching. The film can be stretched even in an aqueous solution such as boric acid or potassium iodide or in a water bath.

  As a material for forming the transparent protective film provided on one side or both sides of the polarizer, a material excellent in transparency, mechanical strength, thermal stability, moisture barrier property, isotropy and the like is preferable. For example, polyester polymers such as polyethylene terephthalate and polyethylene naphthalate, cellulose polymers such as diacetyl cellulose and triacetyl cellulose, acrylic polymers such as polymethyl methacrylate, styrene such as polystyrene and acrylonitrile / styrene copolymer (AS resin) -Based polymer, polycarbonate-based polymer and the like. In addition, polyethylene, polypropylene, polyolefins having a cyclo or norbornene structure, polyolefin polymers such as ethylene / propylene copolymers, vinyl chloride polymers, amide polymers such as nylon and aromatic polyamide, imide polymers, sulfone polymers , Polyether sulfone polymer, polyether ether ketone polymer, polyphenylene sulfide polymer, vinyl alcohol polymer, vinylidene chloride polymer, vinyl butyral polymer, arylate polymer, polyoxymethylene polymer, epoxy polymer, or the above Polymer blends and the like are also examples of polymers that form the transparent protective film. The transparent protective film can also be formed as a cured layer of thermosetting or ultraviolet curable resin such as acrylic, urethane, acrylurethane, epoxy, and silicone.

  Moreover, the polymer film described in JP-A-2001-343529 (WO01 / 37007), for example, (A) a thermoplastic resin having a substituted and / or unsubstituted imide group in the side chain, and (B) a substitution in the side chain And / or a resin composition containing a thermoplastic resin having unsubstituted phenyl and a nitrile group. A specific example is a film of a resin composition containing an alternating copolymer composed of isobutylene and N-methylmaleimide and an acrylonitrile / styrene copolymer. As the film, a film made of a mixed extruded product of the resin composition or the like can be used.

  Although the thickness of a protective film can be determined suitably, generally it is about 1-500 micrometers from points, such as workability | operativity, such as intensity | strength and handleability, and thin film property. In particular, 5 to 200 μm is preferable.

  Moreover, it is preferable that a protective film has as little color as possible. Therefore, Rth = (nx−nz) · d (where nx is the refractive index in the slow axis direction in the film plane, nz is the refractive index in the film thickness direction, and d is the film thickness). A protective film having a direction retardation of −90 nm to +75 nm is preferably used. By using a film having a thickness direction retardation value (Rth) of −90 nm to +75 nm, coloring (optical coloring) of the polarizing plate caused by the protective film can be almost eliminated. The thickness direction retardation (Rth) is more preferably -80 nm to +60 nm, and particularly preferably -70 nm to +45 nm.

  As the protective film, a cellulose polymer such as triacetyl cellulose is preferable from the viewpoints of polarization characteristics and durability. A triacetyl cellulose film is particularly preferable. In addition, when providing a protective film on both sides of a polarizer, the protective film which consists of the same polymer material may be used by the front and back, and the protective film which consists of a different polymer material etc. may be used.

  The polarizer and the protective film are usually in close contact with each other through an aqueous adhesive or the like. Examples of the water-based adhesive include an isocyanate-based adhesive, a polyvinyl alcohol-based adhesive, a gelatin-based adhesive, a vinyl-based latex, a water-based polyurethane, and a water-based polyester.

  The surface of the transparent protective film to which the polarizer is not adhered may be subjected to a treatment for the purpose of hard coat layer, antireflection treatment, sticking prevention, diffusion or antiglare.

  The hard coat treatment is applied for the purpose of preventing scratches on the surface of the polarizing plate. For example, a transparent protective film with a cured film excellent in hardness, sliding properties, etc. by an appropriate ultraviolet curable resin such as acrylic or silicone is used. It can be formed by a method of adding to the surface of the film. The antireflection treatment is performed for the purpose of preventing reflection of external light on the surface of the polarizing plate, and can be achieved by forming an antireflection film or the like according to the conventional art. Further, the anti-sticking treatment is performed for the purpose of preventing adhesion with an adjacent layer.

  The anti-glare treatment is applied for the purpose of preventing the outside light from being reflected on the surface of the polarizing plate and obstructing the visibility of the light transmitted through the polarizing plate. For example, the surface is roughened by a sandblasting method or an embossing method. It can be formed by imparting a fine concavo-convex structure to the surface of the transparent protective film by an appropriate method such as a blending method of transparent fine particles. The fine particles to be included in the formation of the surface fine concavo-convex structure are, for example, conductive materials made of silica, alumina, titania, zirconia, tin oxide, indium oxide, cadmium oxide, antimony oxide or the like having an average particle size of 0.5 to 50 μm. In some cases, transparent fine particles such as inorganic fine particles, organic fine particles composed of a crosslinked or uncrosslinked polymer, and the like are used. When forming a surface fine uneven structure, the amount of fine particles used is generally about 2 to 50 parts by weight, preferably 5 to 25 parts by weight, based on 100 parts by weight of the transparent resin forming the surface fine uneven structure. The antiglare layer may also serve as a diffusion layer (viewing angle expanding function or the like) for diffusing the light transmitted through the polarizing plate to expand the viewing angle.

  The antireflection layer, antisticking layer, diffusing layer, antiglare layer and the like can be provided on the transparent protective film itself, or can be provided separately from the transparent protective layer as an optical layer.

  In addition, as an optical film, for example, it is used for forming a liquid crystal display device such as a reflection plate, an anti-transmission plate, a retardation plate (including wavelength plates such as 1/2 and 1/4), a viewing angle compensation film, and a brightness enhancement film. And an optical layer that may be formed. These can be used alone as an optical film, or can be laminated on the polarizing plate for practical use and used as one layer or two or more layers.

  In particular, a reflective polarizing plate or a semi-transmissive polarizing plate in which a polarizing plate is further laminated with a reflecting plate or a semi-transmissive reflecting plate, an elliptical polarizing plate or a circular polarizing plate in which a retardation plate is further laminated on a polarizing plate, a polarizing plate A wide viewing angle polarizing plate in which a viewing angle compensation film is further laminated on a plate, or a polarizing plate in which a brightness enhancement film is further laminated on a polarizing plate is preferable.

  A reflective polarizing plate is a polarizing plate provided with a reflective layer, and is used to form a liquid crystal display device or the like that reflects incident light from the viewing side (display side). Such a light source can be omitted, and the liquid crystal display device can be easily thinned. The reflective polarizing plate can be formed by an appropriate method such as a method in which a reflective layer made of metal or the like is attached to one surface of the polarizing plate via a transparent protective layer or the like as necessary.

  Specific examples of the reflective polarizing plate include those in which a reflective layer is formed by attaching a foil or a vapor deposition film made of a reflective metal such as aluminum on one side of a transparent protective film matted as necessary. In addition, the transparent protective film may contain fine particles to form a surface fine concavo-convex structure, and a reflective layer having a fine concavo-convex structure thereon. The reflective layer having the fine concavo-convex structure has an advantage that incident light is diffused by irregular reflection to prevent directivity and glaring appearance and to suppress unevenness in brightness and darkness. Moreover, the protective film containing fine particles also has an advantage that incident light and its reflected light are diffused when passing through it and light and dark unevenness can be further suppressed. The reflective layer of the fine concavo-convex structure reflecting the surface fine concavo-convex structure of the transparent protective film is formed by, for example, applying metal to the surface of the transparent protective layer by an appropriate method such as a vacuum deposition method, an ion plating method, a sputtering method, or a plating method. It can be performed by a method of attaching directly to the screen.

  Instead of the method of directly applying the reflecting plate to the transparent protective film of the polarizing plate, the reflecting plate can be used as a reflecting sheet provided with a reflecting layer on an appropriate film according to the transparent film. Since the reflective layer is usually made of metal, the usage form in which the reflective surface is covered with a transparent protective film, a polarizing plate or the like is used to prevent the reflectance from being lowered due to oxidation, and thus to maintain the initial reflectance for a long time. In addition, it is more preferable to avoid a separate attachment of the protective layer.

  The semi-transmissive polarizing plate can be obtained by using a semi-transmissive reflective layer such as a half mirror that reflects and transmits light with the reflective layer. A transflective polarizing plate is usually provided on the back side of a liquid crystal cell, and displays an image by reflecting incident light from the viewing side (display side) when a liquid crystal display device is used in a relatively bright atmosphere. In a relatively dark atmosphere, a liquid crystal display device of a type that displays an image using a built-in power source such as a backlight built in the back side of the transflective polarizing plate can be formed. In other words, the transflective polarizing plate can be used to form liquid crystal display devices that can save energy when using a light source such as a backlight in a bright atmosphere and can be used with a built-in power supply even in a relatively dark atmosphere. It is.

  An elliptically polarizing plate or a circularly polarizing plate in which a retardation plate is further laminated on a polarizing plate will be described. A phase difference plate or the like is used when changing linearly polarized light to elliptically polarized light or circularly polarized light, changing elliptically polarized light or circularly polarized light to linearly polarized light, or changing the polarization direction of linearly polarized light. In particular, a so-called quarter-wave plate (also referred to as a λ / 4 plate) is used as a retardation plate that changes linearly polarized light into circularly polarized light or changes circularly polarized light into linearly polarized light. A half-wave plate (also referred to as a λ / 2 plate) is usually used when changing the polarization direction of linearly polarized light.

  The elliptically polarizing plate is effectively used for black and white display without the above color by compensating (preventing) the coloration (blue or yellow) generated by the birefringence of the liquid crystal layer of the super twist nematic (STN) type liquid crystal display device. It is done. Further, the one in which the three-dimensional refractive index is controlled is preferable because it can compensate (prevent) coloring that occurs when the screen of the liquid crystal display device is viewed from an oblique direction. The circularly polarizing plate is effectively used, for example, when adjusting the color tone of an image of a reflective liquid crystal display device in which an image is displayed in color, and also has an antireflection function.

  Examples of the retardation plate include a birefringent film obtained by uniaxially or biaxially stretching a polymer material, a liquid crystal polymer alignment film, and a liquid crystal polymer alignment layer supported by a film. The thickness of the retardation plate is not particularly limited, but is generally about 20 to 150 μm.

  Examples of the polymer material include polyvinyl alcohol, polyvinyl butyral, polymethyl vinyl ether, polyhydroxyethyl acrylate, hydroxyethyl cellulose, hydroxypropyl cellulose, methyl cellulose, polycarbonate, polyarylate, polysulfone, polyethylene terephthalate, polyethylene naphthalate, polyether sulfone, Polyphenylene sulfide, polyphenylene oxide, polyallylsulfone, polyamide, polyimide, polyolefin, polyvinyl chloride, cellulose polymer, norbornene resin, or binary, ternary copolymers, graft copolymers, Examples include blends. These polymer materials become an oriented product (stretched film) by stretching or the like.

  Examples of the liquid crystal polymer include various main chain types and side chain types in which a conjugated linear atomic group (mesogen) imparting liquid crystal alignment is introduced into the main chain or side chain of the polymer. . Specific examples of the main chain type liquid crystal polymer include a nematic alignment polyester liquid crystal polymer, a discotic polymer, and a cholesteric polymer having a structure in which a mesogen group is bonded at a spacer portion that imparts flexibility. Specific examples of the side chain type liquid crystal polymer include polysiloxane, polyacrylate, polymethacrylate, or polymalonate as a main chain skeleton, and a nematic alignment-providing para-substitution through a spacer portion composed of a conjugated atomic group as a side chain. Examples thereof include those having a mesogenic part composed of a cyclic compound unit. These liquid crystal polymers are prepared by, for example, applying a solution of a liquid crystalline polymer on an alignment treatment surface such as a surface of a thin film such as polyimide or polyvinyl alcohol formed on a glass plate, or an oblique deposition of silicon oxide. This is done by developing and heat treatment.

  The retardation plate may have an appropriate retardation according to the purpose of use, such as those for the purpose of compensating for various wavelength plates or birefringence of liquid crystal layers and compensation of viewing angle, etc. It may be one in which retardation plates are stacked and optical characteristics such as retardation are controlled.

  The elliptical polarizing plate and the reflective elliptical polarizing plate are obtained by laminating a polarizing plate or a reflective polarizing plate and a retardation plate in an appropriate combination. Such an elliptically polarizing plate or the like can also be formed by sequentially laminating them sequentially in the manufacturing process of the liquid crystal display device so as to be a combination of a (reflective) polarizing plate and a retardation plate. An optical film such as a polarizing plate has an advantage that it can improve the production efficiency of a liquid crystal display device and the like because of excellent quality stability and lamination workability.

  The viewing angle compensation film is a film for widening the viewing angle so that an image can be seen relatively clearly even when the screen of the liquid crystal display device is viewed from a slightly oblique direction rather than perpendicular to the screen. As such a viewing angle compensation phase difference plate, for example, a phase difference plate, an alignment film such as a liquid crystal polymer, or an alignment layer such as a liquid crystal polymer supported on a transparent substrate is used. A normal retardation plate uses a birefringent polymer film uniaxially stretched in the plane direction, whereas a retardation plate used as a viewing angle compensation film stretches biaxially in the plane direction. Birefringent polymer film, biaxially stretched film such as polymer with birefringence with a controlled refractive index in the thickness direction that is uniaxially stretched in the plane direction and stretched in the thickness direction, etc. Used. Examples of the inclined alignment film include a film obtained by bonding a heat shrink film to a polymer film and stretching or / and shrinking the polymer film under the action of the contraction force by heating, and a film obtained by obliquely aligning a liquid crystal polymer. can give. The raw material polymer for the phase difference plate is the same as the polymer described in the previous phase difference plate, preventing coloration due to a change in the viewing angle based on the phase difference by the liquid crystal cell and expanding the viewing angle for good visual recognition. An appropriate one for the purpose can be used.

  In addition, from the viewpoint of achieving a wide viewing angle with good visibility, an optical compensation position in which an alignment layer of a liquid crystal polymer, particularly an optically anisotropic layer composed of a tilted alignment layer of a discotic liquid crystal polymer, is supported by a triacetyl cellulose film. A phase difference plate can be preferably used.

  A polarizing plate obtained by bonding a polarizing plate and a brightness enhancement film is usually provided on the back side of a liquid crystal cell. The brightness enhancement film reflects a linearly polarized light with a predetermined polarization axis or a circularly polarized light in a predetermined direction when natural light is incident due to a backlight such as a liquid crystal display device or reflection from the back side, and transmits other light. In addition, a polarizing plate in which a brightness enhancement film is laminated with a polarizing plate allows light from a light source such as a backlight to enter to obtain transmitted light in a predetermined polarization state, and reflects light without transmitting the light other than the predetermined polarization state. The The light reflected on the surface of the brightness enhancement film is further inverted through a reflective layer or the like provided behind the brightness enhancement film and re-incident on the brightness enhancement film, and part or all of the light is transmitted as light having a predetermined polarization state. Luminance can be improved by increasing the amount of light transmitted through the enhancement film and increasing the amount of light that can be used for liquid crystal display image display or the like by supplying polarized light that is difficult to be absorbed by the polarizer. That is, when light is incident through the polarizer from the back side of the liquid crystal cell without using a brightness enhancement film, light having a polarization direction that does not coincide with the polarization axis of the polarizer is almost polarized. It is absorbed by the polarizer and does not pass through the polarizer. That is, although depending on the characteristics of the polarizer used, approximately 50% of the light is absorbed by the polarizer, and accordingly, the amount of light that can be used for liquid crystal image display or the like is reduced and the image becomes dark. The brightness enhancement film reflects light that has a polarization direction that is absorbed by the polarizer without being incident on the polarizer, and is reflected by the brightness enhancement film, and then inverted through a reflective layer or the like provided behind the brightness enhancement film. The brightness enhancement film transmits only the polarized light in which the polarization direction of the light reflected and inverted between the two is allowed to pass through the polarizer. Since the light is supplied to the polarizer, light such as a backlight can be efficiently used for displaying an image on the liquid crystal display device, and the screen can be brightened.

  A diffusion plate may be provided between the brightness enhancement film and the reflective layer. The polarized light reflected by the brightness enhancement film is directed to the reflective layer or the like, but the installed diffuser plate uniformly diffuses the light passing therethrough and simultaneously cancels the polarized state and becomes a non-polarized state. That is, the light in the natural light state is directed toward the reflection layer or the like, reflected through the reflection layer or the like, and again passes through the diffusion plate and reenters the brightness enhancement film. In this way, by providing a diffuser plate that returns polarized light to the original natural light between the brightness enhancement film and the reflective layer, the brightness of the display screen is maintained, and at the same time, the brightness of the display screen is reduced and uniform. Can provide a bright screen. By providing such a diffuser plate, it is considered that the first incident light has a moderate increase in the number of repetitions of reflection, and in combination with the diffusion function of the diffuser plate, a uniform bright display screen can be provided.

  The brightness enhancement film has a characteristic of transmitting linearly polarized light having a predetermined polarization axis and reflecting other light, such as a multilayer thin film of dielectric material or a multilayer laminate of thin film films having different refractive index anisotropies. Such as an alignment film of a cholesteric liquid crystal polymer or an alignment liquid crystal layer supported on a film substrate, which reflects either left-handed or right-handed circularly polarized light and transmits other light. Appropriate things, such as a thing, can be used.

  Therefore, in the brightness enhancement film of the type that transmits linearly polarized light having the predetermined polarization axis as described above, the transmitted light is incident on the polarizing plate with the polarization axis aligned as it is, thereby efficiently transmitting while suppressing absorption loss due to the polarizing plate. Can be made. On the other hand, in a brightness enhancement film of a type that transmits circularly polarized light such as a cholesteric liquid crystal layer, it can be incident on a polarizer as it is, but from the point of suppressing absorption loss, the circularly polarized light is converted into linearly polarized light through a retardation plate. It is preferably incident on the polarizing plate. Note that circularly polarized light can be converted to linearly polarized light by using a quarter wave plate as the retardation plate.

  A retardation plate that functions as a quarter-wave plate at a wide wavelength in the visible light region or the like exhibits, for example, a retardation plate that functions as a quarter-wave plate for light-colored light having a wavelength of 550 nm and other retardation characteristics. It can be obtained by a method in which a phase difference layer, for example, a phase difference layer that functions as a half-wave plate is superimposed. Therefore, the retardation plate disposed between the polarizing plate and the brightness enhancement film may be composed of one or more retardation layers.

  In addition, a cholesteric liquid crystal layer having a reflection structure that reflects circularly polarized light in a wide wavelength range such as a visible light range can be obtained by combining two or more layers with different reflection wavelengths to form an overlapping structure. Based on this, transmitted circularly polarized light in a wide wavelength range can be obtained.

  Further, the polarizing plate may be formed by laminating a polarizing plate and two or more optical layers as in the above-described polarization separation type polarizing plate. Therefore, a reflective elliptical polarizing plate or a semi-transmissive elliptical polarizing plate in which the above-described reflective polarizing plate or semi-transmissive polarizing plate and a retardation plate are combined may be used.

  An optical film in which the optical layer is laminated on a polarizing plate can be formed by a method of sequentially laminating separately in the manufacturing process of a liquid crystal display device or the like. There is an advantage that the manufacturing process of a liquid crystal display device or the like can be improved because of excellent stability and assembly work. For the lamination, an appropriate adhesive means such as an adhesive layer can be used. When bonding the polarizing plate and the other optical layer, their optical axes can be set at an appropriate arrangement angle in accordance with the target retardation characteristics.

  In addition, in each layer such as an optical film and an adhesive layer of the optical film with an adhesive of the present invention, for example, a salicylic acid ester compound, a benzophenol compound, a benzotriazole compound, a cyanoacrylate compound, a nickel complex compound, etc. What gave the ultraviolet absorptivity by systems, such as a system processed with a ultraviolet absorber, etc. may be used.

  The optical film with an adhesive of the present invention can be preferably used for forming various image display devices such as a liquid crystal display device. The liquid crystal display device can be formed according to the conventional method. That is, a liquid crystal display device is generally formed by appropriately assembling components such as a liquid crystal cell, an optical film with an adhesive, and a lighting system as necessary, and incorporating a drive circuit. There is no limitation in particular except the point which uses the optical film by invention, and it can apply according to the former. As the liquid crystal cell, an arbitrary type such as an arbitrary type such as a TN type, an STN type, or a π type can be used.

  Appropriate liquid crystal display devices such as a liquid crystal display device in which an optical film with an adhesive is disposed on one side or both sides of a liquid crystal cell and a backlight or a reflector used in an illumination system can be formed. In that case, the optical film according to the present invention can be installed on one side or both sides of the liquid crystal cell. When optical films are provided on both sides, they may be the same or different. Further, when forming a liquid crystal display device, for example, a single layer or a suitable part such as a diffusing plate, an antiglare layer, an antireflection film, a protective plate, a prism array, a lens array sheet, a light diffusing plate, a backlight, etc. Two or more layers can be arranged.

  EXAMPLES The present invention will be specifically described below with reference to examples, but the present invention is not limited to these examples. In addition, all the parts and% in each example are based on weight.

Example 1
(Production of optical film)
A 80 μm-thick polyvinyl alcohol film was stretched 5 times in an aqueous iodine solution at 40 ° C. and then dried at 50 ° C. for 4 minutes to obtain a polarizer. A triacetyl cellulose film was bonded to both sides of this polarizer using a polyvinyl alcohol-based adhesive to obtain a polarizing plate.

(Preparation of adhesive solution)
A solution containing an acrylic polymer having a weight average molecular weight of 2 million consisting of a copolymer of butyl acrylate: acrylic acid: 2-hydroxyethyl acrylate = 100: 5: 0.1 (weight ratio) as a base polymer (solid content 24 %, The solvent component was ethyl acetate, boiling point 77 ° C.). To the above acrylic polymer solution, 3.2 parts of Coronate L manufactured by Nippon Polyurethane Co., Ltd., which is an isocyanate-based polyfunctional compound, is added to the polymer solid content of 100 parts, and an additive (KBM-403, manufactured by Shin-Etsu Silicone Co.) 6 parts of a diluent solvent (toluene, boiling point 110 ° C.) for viscosity adjustment was added to prepare an adhesive solution (solid content of acrylic polymer 11%).

(Preparation of adhesive optical film)
The pressure-sensitive adhesive solution was applied on a release film (polyethylene terephthalate base material: Diafoil MRF38, manufactured by Mitsubishi Chemical Polyester Co., Ltd.) with a coating thickness of 250 μm using a comma coater. It was dried in a drying oven set to a pressure-sensitive adhesive layer having a thickness of 20 μm. The distance from the comma coater to the drying oven was 1 m, and the coating speed was 2 m / min. Moreover, the heating roll which passed 40 degreeC warm water was installed in the position of 50 cm from the comma coater, and it heated by making the back surface contact the said heating roll with respect to the coating surface of a release film. The atmospheric environment from the comma coater to the drying oven was 25 ° C. and 70% RH. The dew point temperature in the atmospheric environment is 20 ° C. When the temperature of the release film was measured at a position 20 cm before the drying oven, it was 32.1 ° C.

  Using the above polarizing plate as an optical film, the pressure-sensitive adhesive layer formed on the release film after oven drying was bonded with the polarizing plate and a laminator roll to obtain an adhesive polarizing plate.

Example 2
In Example 1, the pressure-sensitive adhesive mold was the same as Example 1 except that the solid content concentration of the acrylic polymer in the pressure-sensitive adhesive solution was changed to 5% and the coating thickness of the pressure-sensitive adhesive solution was changed to 500 μm. A polarizing plate was produced.

Example 3
In Example 1, the pressure-sensitive adhesive polarizing plate was changed in the same manner as in Example 1 except that the temperature of the hot water passed through the heating roll was changed to 70 ° C. and the temperature of the drying oven was changed to 50 ° C. Produced.

Example 4
In Example 1, an adhesive polarizing plate was produced in the same manner as in Example 1 except that the adhesive solution was heated to 40 ° C. and applied, and the temperature of the drying oven was changed to 50 ° C. .

Example 5
In Example 1, as an optical film, a retardation plate (thickness: 80 μm) made of a uniaxially stretched norbornene resin (manufactured by JSR, trade name Arton) and having a corona-treated surface was used instead of a polarizing plate. Except for this, an adhesive type retardation plate was produced in the same manner as in Example 1.

Comparative Example 1
In Example 1, an adhesive polarizing plate was produced in the same manner as in Example 1, except that the release film was not adhered to the heating roll and the temperature of the drying oven was changed to 50 ° C.

Comparative Example 2
In Comparative Example 1, Examples were used except that 1.2 parts of a tetrafunctional epoxy crosslinking agent (trade name Tetrad D; manufactured by Mitsubishi Gas Chemical Company) was used in place of Coronate L as the crosslinking agent in the adhesive solution. In the same manner as in Example 1, an adhesive polarizing plate was produced.

  The following evaluation was performed about the adhesion type polarizing plate or adhesion type phase difference plate obtained by the said Example and comparative example. The evaluation results are shown in Table 1. In addition, it shows in Table 1 also about the temperature of the release film measured in the position of 20 cm before the drying oven in each example. The temperature of the release film was measured using a contact film thermometer (Tc-700 manufactured by LINE Seiki Co., Ltd.) on the back surface of the release film.

(Appearance evaluation)
The appearance of the obtained pressure-sensitive adhesive polarizing plate or pressure-sensitive retardation plate was visually evaluated as transparent or cloudy. In the examples, no condensation was observed in the adhesive layer solution (coating film) on the release film between the comma coater and the drying oven. On the other hand, in Comparative Examples 1 and 2, condensation was observed.

(Haze)
According to haze (cloudiness) of JIS K7136 (1981 version), it was measured using a haze meter HM150 type (trade name, manufactured by Murakami Color Research Laboratory Co., Ltd.).

(Throwing property)
The prepared adhesive polarizing plate or adhesive retardation plate was cut into a width of 25 mm and a length of 50 mm. After bonding the adhesive layer surface and the surface of the 50 μm thick polyethylene terephthalate film so that the vapor deposition surface of the vapor deposition film deposited with indium-tin oxide is in contact with each other, the environment is kept at 23 ° C./60% RH for 20 minutes or more. Left alone. Then, after peeling off the edge part of a polyethylene terephthalate film by hand and confirming that the adhesive has adhered to the polyethylene terephthalate film side, using a tensile tester (Shimadzu Corporation autograph AG-1) Then, the adhesion (N / 25 mm) between the optical film and the pressure-sensitive adhesive layer was measured at 180 ° peeling and at a tensile speed of 300 mm / min in a room temperature atmosphere (25 ° C.). About each sample, three points | pieces were measured and it was set as the average value.

It is an example of the conceptual diagram which shows the manufacturing method of the adhesive optical film of this invention.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Release film 2 Adhesive layer 3 Optical film 11 Die coater 12 Drying oven 13 Heating roll 14 Transfer roll 21 Adhesive solution

Claims (3)

A step (1) of applying a pressure-sensitive adhesive solution containing a pressure-sensitive adhesive and a solvent to at least one surface of the release film , and a step of forming a pressure-sensitive adhesive layer by removing the solvent by subjecting the pressure-sensitive adhesive solution to a drying treatment (2) ) look including the and the release film, the coating step (1), after the drying process was performed (2), the formed release film adhesive layer, a step of transferring the optical film (3) In the method for producing an adhesive optical film having an adhesive layer on at least one surface of the optical film,
The pressure-sensitive adhesive contains an acrylic polymer as a base polymer, and contains an isocyanate compound as a crosslinking agent,
The so as not to cause condensation on the coated cohesive adhesive solution to a release film, said after performing the coating step (1), the temperature of the release film to the drying step (2), the release The pressure-sensitive adhesive layer formed after the drying step (2) is controlled to a temperature not lower than the dew point in the atmospheric environment where the film is placed and not higher than the boiling point of the solvent in the pressure-sensitive adhesive solution. Haze is 0.3% or less, The manufacturing method of the adhesive optical film characterized by the above-mentioned. The temperature control of the release film was subjected to a coating step (1), until the drying step (2), pressure-sensitive adhesive optical according to claim 1, characterized in that by providing a heating roll A method for producing a film. Temperature of the heating roll, the temperature of the release film that has passed through the heating roll, than the ambient environmental temperature, according to claim 2, wherein the set to a temperature higher than at least 5 ° C. Method for producing an adhesive optical film.

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