JP4765251B2 - Electromagnetic shielding film - Google Patents

Description

  The present invention relates to an electromagnetic wave shielding film, and more particularly to an electromagnetic wave shielding film that can be used as a liquid crystal display panel member to prevent malfunction of electronic equipment due to electromagnetic waves without reducing visibility. is there.

  In the liquid crystal display device, an STN type or TFT type color liquid crystal display panel and a backlight unit disposed on the back surface of the panel are accommodated in a case.

  In the liquid crystal display panel, a liquid crystal layer is interposed between two transparent glasses, and a driving IC is provided on a transparent glass substrate or a circuit substrate.

  The liquid crystal display device having such a configuration is known to have a problem that noise is mixed into the liquid crystal display unit due to electromagnetic waves emitted from the backlight of the device.

  Recently, as the liquid crystal display panel becomes larger (20 inches or more), the fluorescent lamp of the backlight unit is arranged directly under the liquid crystal display panel, and the number of fluorescent lamps increases. The problem of malfunctioning is increasing.

On the other hand, as an electromagnetic wave shielding film, a conductive thin film layer made of a metal oxide and a metal thin film layer are alternately laminated on a transparent base material, and indium oxide (In2O3) is formed as a conductive thin film layer made of a metal oxide. ) And tin oxide (SnO2) ) Of a mixed sintered body (hereinafter referred to as ITO) (see, for example, Patent Documents 1 and 2).
JP 2000-62082 A JP 2001-210987 A

  However, the electromagnetic wave shielding film as described above is excellent in electromagnetic wave shielding properties and good transparency, but is very expensive because a large number of thin film layers are laminated. Therefore, in principle, it is only used for a plasma display panel (PDP) or the like in which electromagnetic waves are strongly emitted. On the other hand, in the case of a liquid crystal display panel (LCD), which is another typical thin and large display, electromagnetic waves emitted from the fluorescent lamp of the backlight are much less than in the case of the PDP. Therefore, at present, an electromagnetic wave shielding film in which an ITO film that is cheaper than the electromagnetic wave shielding film having the multilayer thin film structure is provided on a transparent substrate is used between the liquid crystal display panel and the backlight unit.

  However, in a conventional electromagnetic wave shielding film having a configuration in which an ITO layer is provided on a transparent substrate, the transparent conductive film (ITO film) itself is colored and has a low transmittance in the visible light region. There was a problem that visibility was lowered.

  An object of the present invention is to provide an electromagnetic wave shielding film having high light transmittance, extremely little coloring, and good electromagnetic wave shielding characteristics. It is another object of the present invention to provide an electromagnetic wave shielding film having excellent adhesion between the electromagnetic wave shielding layer and the protective layer, and having excellent visibility even after being stored for a long time under high temperature and high humidity.

  This invention was made | formed in view of the above situations, Comprising: The electromagnetic wave shielding film which was able to solve said subject is as follows.

That is, the first invention of the present invention is the ionic group concentration obtained by crosslinking a transparent polymer film (A), a transparent conductive layer (B), and a polyester resin into which an ionic group is introduced with a crosslinking agent. And a protective layer (C) having a refractive index of 1.40 or more and 1.70 or less , laminated in this order, and having a wavelength of 550 nm. The electromagnetic wave shielding film is characterized by having a light transmittance of 90% or more.

2nd invention has a refractive index more than a transparent polymer film (A) on the surface opposite to the surface which laminated | stacked the transparent conductive layer (B) and protective layer (C) of the said transparent polymer film (A). The electromagnetic wave shielding film according to the first invention, wherein a low layer (D) is provided.

  The electromagnetic wave shielding film according to the present invention has a structure in which a transparent polymer film (A), a transparent conductive layer (B), and a protective layer (C) are sequentially laminated, has high light transmittance, and is extremely colored. In addition, since the electromagnetic wave shielding characteristics are good, the malfunction of the liquid crystal can be prevented, particularly when incorporated in a large liquid crystal display panel, and the visibility of the display is excellent. Furthermore, by using a protective layer composed of a resin having a specific ionic group concentration and a crosslinked structure, the adhesion between the transparent conductive layer and the protective layer is improved. There is an advantage of excellent visibility even after storage for a period.

  The electromagnetic wave shielding film of the present invention is an electromagnetic wave shielding film having a transparent polymer film (A), a transparent conductive layer (B), and a protective layer (C), preventing oxidation deterioration of the transparent conductive layer (B), From the viewpoint of preventing scratches, etc., it has a laminated structure of A / B / C. Moreover, you may provide a transparent conductive layer (B) and a protective layer (C) on both surfaces of a transparent polymer film (A), and also provide a transparent conductive layer (B) and a protective layer (C) on one side of A layer. A plurality of them may be provided. For example, a laminated structure such as C / B / A / B / C, A / B / C / B / C, and the like can be given.

  The transparent polymer film in the present invention is a film obtained by subjecting an organic polymer to melt extrusion or solution extrusion and, if necessary, stretching, cooling, and heat setting in the longitudinal direction and / or the width direction. Organic polymers include polyethylene, polypropylene, polyethylene terephthalate, polyethylene-2, 6-naphthalate, polypropylene terephthalate, nylon 6, nylon 4, nylon 66, nylon 12, polyimide, polyamideimide, polyethersulfane, polyetheretherketone , Polycarbonate, polyarylate, cellulose propionate, polyvinyl chloride, polyvinylidene chloride, polyvinyl alcohol, polyetherimide, polyphenylene sulfide, polyphenylene oxide, polystyrene, syndiotactic polystyrene, norbornene-based polymer, and the like. These organic polymers may be copolymerized or blended with a small amount of other organic polymers. Among these, polyethylene terephthalate, polypropylene terephthalate, polyethylene-2,6-naphthalate, syndiotactic polystyrene, norbornene-based polymer and the like are preferably used, and polyethylene terephthalate is particularly preferable.

  The transparent polymer film (A) used in the present invention preferably has a thickness in the range of more than 10 μm and not more than 300 μm, particularly preferably in the range of 70 to 260 μm. When the thickness of the film is less than 10 μm, the transparent polymer film of the substrate is easily deformed by radiant heat when forming the transparent conductive layer, and when it exceeds 250 μm, the flexibility of the film is lowered and the handling property is lowered. It is easy for problems to occur.

  As the transparent polymer film (A) used in the present invention, a biaxially oriented film is preferable from the viewpoint of mechanical strength, dimensional stability, chemical resistance, and the like.

  Further, in order to improve the adhesion between the transparent polymer film (A) and the transparent conductive layer (B), the surface of the transparent polymer film is preliminarily roughened using corona discharge treatment, plasma treatment, and sandblasting. You may provide surface treatments, such as surface treatment, or provide the well-known adhesive property modification layer comprised from adhesive property modification resin as those intermediate layers.

As a constituent material of the transparent conductive layer (B) provided between the transparent polymer film (A) and the protective layer (C), In 2 O 3 Metal oxides such as SnO2, ITO, and zinc oxide (ZnO) are suitable. Among these, ITO is particularly preferable in terms of transparency and conductivity. 10-100 nm is preferable and, as for the film thickness of a transparent conductive layer (B), 20-80 nm is more preferable. If the film thickness of the transparent conductive layer (B) is less than 10 nm, it is difficult to obtain sufficient electromagnetic wave shielding characteristics. On the other hand, when the film thickness of the transparent conductive layer (B) exceeds 100 nm, the bending resistance and the light transmittance tend to be lowered.

  As a method for forming the transparent conductive layer (B) on the transparent polymer film (A) or the protective layer (C), there are various film forming methods such as a vacuum deposition method, a sputtering method, and an ion plating method. Among these, the sputtering method is preferable in terms of adhesion and stability.

The protective layer (C) provided on the transparent polymer film (A) or the transparent conductive layer (B) has a refractive index in the range of 1.40 or more and 1.70 or less to improve transparency, and display It is preferable from the viewpoint of improving the visibility when it is incorporated. As a general low refractive material, inorganic materials include SiO ₂ (1.46) and CaF ₂ (1.38). However, CaF ₂ is not preferable because it does not have water resistance (is soluble in water). Moreover, although a fluorine-containing polymer is mentioned with an organic substance, 1.40 is a minimum in what can be obtained commercially. On the other hand, if the refractive index exceeds 1.70, the light transmittance tends to decrease. For example, when ITO is used as the material of the transparent conductive layer (B), since the refractive index of ITO is 1.9 to 2.0, when the refractive index of the protective layer (C) exceeds 1.70, the wavelength is 550 nm. It becomes difficult to set the light transmittance at 90% or more.

  Furthermore, in order to obtain long-term stable electromagnetic shielding properties and visibility, it is preferable to improve the adhesion between the protective layer (C) and the transparent conductive layer (B). Examples of the protective layer (C) having such a function include those composed of a resin containing an ionic group, having an ionic group concentration of 20 to 1000 eq / ton and having a crosslinked structure. In order to introduce an ionic group into the resin, it is preferable to contain an ionic group-containing monomer and copolymerize it when polymerizing the resin as the main chain. Subsequently, it is preferable to crosslink the resin into which the ionic group is introduced with a crosslinking agent.

  As the resin that can be used as the protective layer (C), polyester resin, acrylic resin, urethane resin, melamine resin, methacrylic resin, urethane acrylic resin, silicon acrylic resin, melamine resin, polysiloxane resin and the like are preferable. Among these, a polyester resin is preferable from the viewpoint of productivity.

A polyester resin is generally produced by subjecting a polycarboxylic acid and a polyhydric alcohol to an esterification reaction or a transesterification reaction, followed by polycondensation.
Examples of the polyvalent carboxylic acids include terephthalic acid, isophthalic acid, orthophthalic acid, 1,5-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, diphenic acid, sulfoterephthalic acid, 5-sulfoisophthalic acid, 4 -Sulfophthalic acid, 4-sulfonaphthalene-2,7-dicarboxylic acid, 5 [4-sulfophenoxy] isophthalic acid, sulfoterephthalic acid, and / or their metal salts, ammonium salts and other aromatic dicarboxylic acids, p-oxybenzoic acid Acids, aromatic oxycarboxylic acids such as p- (hydroxyethoxy) benzoic acid, succinic acid, adipic acid, azelaic acid, sebacic acid, dodecanedicarboxylic acid and other aliphatic dicarboxylic acids, fumaric acid, maleic acid, itaconic acid, hexa Unsaturated fats such as hydrophthalic acid, tetrahydrophthalic acid, etc. And alicyclic dicarboxylic acids, etc., and can be exemplified other trimellitic acid as a polycarboxylic acid, trimesic acid, and the like trivalent or higher polyvalent carboxylic acids such as pyromellitic acid.

  Examples of the polyhydric alcohols include aliphatic polyhydric alcohols, alicyclic polyhydric alcohols, and aromatic polyhydric alcohols.

  Aliphatic polyhydric alcohols include ethylene glycol, propylene glycol, 1,3-propanediol, 2,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, Neopentyl glycol, diethylene glycol, dipropylene glycol, 2,2,4-trimethyl-1,3-pentanediol, aliphatic diols such as polyethylene glycol, polypropylene glycol, polytetramethylene glycol, trimethylolethane, trimethylolpropane, Examples include triols and tetraols such as glycerin and pentaelsitol.

  Alicyclic polyhydric alcohols include 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, spiroglycol, hydrogenated bisphenol A, ethylene oxide adduct and propylene oxide adduct of hydrogenated bisphenol A, tricyclo Examples include decanediol and tricyclodecane dimethanol.

  As aromatic polyhydric alcohols, para-xylene glycol, meta-xylene glycol, ortho-xylene glycol, 1,4-phenylene glycol, ethylene oxide adduct of 1,4-phenylene glycol, bisphenol A, ethylene oxide adduct of bisphenol A And propylene oxide adducts.

  Furthermore, examples of polyester polyols include lactone polyester polyols obtained by ring-opening polymerization of lactones such as ε-caprolactone. In addition to these, a monofunctional monomer may be introduced into the polyester for the purpose of blocking the polar group at the end of the polyester polymer.

Monofunctional monomers include benzoic acid, chlorobenzoic acid, bromobenzoic acid, parahydroxybenzoic acid, sulfobenzoic acid monoammonium salt, sulfobenzoic acid monosodium salt, cyclohexylaminocarbonylbenzoic acid, n-dodecylaminocarbonylbenzoic acid Acid, tertiary butylbenzoic acid, naphthalenecarboxylic acid, 4-methylbenzoic acid, 3-methylbenzoic acid, salicylic acid, thiosalicylic acid, phenylacetic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, octanecarboxylic acid, lauric acid, stearyl Monocarboxylic acids such as acids and lower alkyl esters thereof, or monoalcohols such as aliphatic alcohols, aromatic alcohols, and alicyclic alcohols can be used.
In the present invention, an unsaturated monomer among these is an essential component, and other components are appropriately selected depending on the glass transition temperature of the polyester resin, the compatibility with the monomer, and the like.

  As the ionic group introduced into the polyester resin, mono- or dicarboxylic acid having an alkali metal sulfonate or ammonium sulfonate group can be preferably used, and for example, an alkali metal carboxylate or ammonium carboxylate base is used. Monomers, anionic groups such as sulfuric acid group, phosphoric acid group, phosphonic acid group, phosphinic acid group or their ammonium salts, metal salts, or cationic group monomers such as primary to tertiary amine groups Etc. can be used.

  When introducing an alkali metal carboxylate base or an ammonium carboxylate base, a carboxyl group is added to the polymer terminal by introducing a polyvalent carboxylic acid such as trimellitic acid into the system at the end of polymerization of the polyester. A method can be used in which this is neutralized with ammonia, sodium hydroxide or the like to exchange with carboxylate groups.

  Moreover, these ionic groups can be introduced into the polyester resin by containing a mono- or dicarboxylic acid having an alkali metal sulfonate group or an ammonium sulfonate group. Examples of the salt include salts of ammonium ions, Li, Na, K, Mg, Ca, Cu, Fe, and the like, and particularly preferable are K salt and Na salt. In the present invention, 5-sodium sulfoisophthalic acid or metasodium sulfobenzoic acid is preferably used. Carboxylate groups and sulfonate groups may also be used.

  In the present invention, the following polyester resins can be exemplified as polyester resins suitable for constituting the protective layer (c).

  a) Polyester resin obtained from polyvalent carboxylic acids containing 80 mol% or more of aromatic monomers, 0 to 90 mol% of ethylene glycol, and 100 to 10 mol% of propylene glycol

  b) Polyester resin obtained from polyvalent carboxylic acids containing 80 mol% or more of aromatic monomers, 5 to 80 mol% of 2,3-butanediol, and 95 to 20 mol% of ethylene glycol.

  c) Polyhydric carboxylic acids containing 80 mol% or more of aromatic monomers, 70 to 95 mol% of C2-C4 aliphatic glycols, and 5 to 30 mol of mono- or polyhydric alcohols having a tricyclodecane skeleton % Polyester resin obtained from

  d) Polyester obtained from polyvalent carboxylic acids containing 80 mol% or more of aromatic monomers, 70 to 95 mol% of C2-C4 aliphatic glycols, and 5 to 30 mol% of hydroxymethyltricyclodecane resin

  e) Polyester obtained from polyvalent carboxylic acids containing 80 mol% or more of aromatic monomers, 70 to 95 mol% of C2-C4 aliphatic glycols, and 5 to 30 mol% of tricyclodecane dimethanol resin

  f) Polyhydric carboxylic acids containing 80 mol% or more of aromatic monomers, 70 to 95 mol% of C2-C4 aliphatic glycols, and 5 to 30 mol% of mono- or polyhydric alcohols having a cyclohexane skeleton Polyester resin obtained from

  g) Polyester resin obtained from polyvalent carboxylic acids containing 80 mol% or more of aromatic monomers, 70 to 95 mol% of C2 to C4 aliphatic glycols, and 5 to 30 mol% of cyclohexanediol.

  h) Polyester resin obtained from polyvalent carboxylic acids containing 80 mol% or more of aromatic monomers, 70 to 95 mol% of C2-C4 aliphatic glycols, and 5 to 30 mol% of hydrogenated biphenol

  i) Polyester resin obtained from polyvalent carboxylic acids containing 80 mol% or more of aromatic monomers, 70 to 95 mol% of C2-C4 aliphatic glycols, and 5 to 30 mol% of hydrogenated bisphenol A

  j) Polyhydric carboxylic acids containing 80 mol% or more of aromatic monomers containing 1 to 20 mol% of mono- or divalent or higher carboxylic acids having a naphthalene skeleton, and 70 to 70 C2 to C4 aliphatic glycols Polyester resin obtained from 100 mol%, polyhydric alcohols containing 0-30 mol% of alicyclic monomers

  Further, the aromatic monomer is preferably terephthalic acid and isophthalic acid. The composition ratio of terephthalic acid and isophthalic acid is preferably 90/10 to 40/60 [mol%], more preferably 80/20 to 50/50 [mol%], and particularly preferably 85/15 to 60 /. 40 [mol%].

  When an ionic group-containing monomer is introduced into a polyester resin and an ionic group is given to the polyester resin, the adhesive force with the transparent conductive thin film becomes strong. As the ionic group-containing monomer, the aforementioned mono- or dicarboxylic acid having an alkali metal sulfonate group or an ammonium sulfonate group can be preferably used. Further, for example, monomers having an alkali metal carboxylate base or an ammonium carboxylate base, sulfuric acid group, phosphoric acid group, phosphonic acid group, phosphinic acid group or their ammonium salts, anionic groups such as metal salts, or the like Cationic group monomers such as primary to tertiary amine groups can be used.

  When introducing an alkali metal carboxylate base or an ammonium carboxylate base, a carboxyl group is added to the polymer terminal by introducing a polyvalent carboxylic acid such as trimellitic acid into the system at the end of polymerization of the polyester. A method can be used in which this is neutralized with ammonia, sodium hydroxide or the like to exchange with carboxylate groups.

  The content of these ionic groups is preferably in the range of 20 to 1000 eq / ton with respect to the polyester resin, including sulfonic acid groups and / or salts thereof. The lower limit of the content of the ionic group is determined from the viewpoint of stably securing adhesion (adhesion between the transparent conductive layer (B) and the protective layer (C)). On the other hand, the upper limit of the content of the ionic group is determined from the viewpoint of stably ensuring heat and humidity resistance, more preferably 500 eq / ton, and particularly preferably 200 eq / ton. Moreover, since heat resistance may be insufficient when it does not have a crosslinked structure, it is preferable to crosslink the polyester resin into which the ionic group is introduced with, for example, an isocyanate-based crosslinking agent.

  The thickness of the protective layer (C) is preferably 30 nm to 300 nm. If the thickness of the protective layer (C) is less than 30 nm, sufficient optical properties may not be obtained, and if it exceeds 300 nm, sufficient light transmittance may not be obtained.

  As a method for forming the protective layer (C), a coating method is preferably used. Coating methods include air doctor coating, knife coating, rod coating, forward rotation roll coating, reverse roll coating, gravure coating, kiss coating, bead coating, slit orifice coating, and cast coating. Used. In the case of imparting a crosslinked structure to the resin constituting the protective layer, it is preferable to apply energy by heating, ultraviolet ray or electron beam irradiation after coating and drying.

  Further, in order to further improve the light transmittance, the surface opposite to the surface where the transparent conductive layer (B) and the protective layer (C) are laminated on the thermoplastic resin film (A) is refracted more than the thermoplastic resin film. It is preferable to provide a low rate layer.

  Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to these examples. In addition, evaluation of the electromagnetic wave shield film obtained by the Example and the comparative example was performed with the following method.

(1) Content of ionic group 0.2 g of resin was dissolved in 20 ml of chloroform and titrated with a 0.1N KOH ethanol solution to obtain an equivalent (eq / ton) per 10 ⁶ g (1 ton) of resin.

(2) Refractive index of resin A resin film obtained by applying and drying a coating liquid containing resin on a Teflon (registered trademark) sheet so that the dried coating film is about 500 μm is obtained from the sheet. It peeled and the sample for a measurement was created. Next, based on JIS-K7142 (Method A), the refractive index of the resin film was measured using an Abbe refractometer (manufactured by Atago Co., Ltd.).

(3) Composition analysis in transparent conductive thin film The weight percentage of tin oxide in the indium-tin composite oxide thin film is the composition of indium and tin in the thin film obtained by atomic absorption analysis. Indium and tin are contained in the thin film. It is a value calculated using the specific gravity of In ₂ O ₃ and SnO ₂ (In ₂ O ₃ is 7.18, SnO ₂ is 6.95) assuming that it is a complete oxide.

(4) Total light transmittance and haze Based on JIS-K7105, the total light transmittance and haze were measured using the haze meter (Nippon Denshoku Industries make, NDH-1001DP).

(5) Light transmittance The light transmittance at a wavelength of 550 nm was measured using a self-recording spectrophotometer (manufactured by Hitachi, U-3500 type).

(6) Color (a value, b value)
In accordance with JIS-K7105, color a and b values were measured with a standard light C / 2 using a color difference meter (manufactured by Nippon Denshoku Industries Co., Ltd., ZE-2000). The color a value is a scale indicating redness, and the higher the numerical value, the stronger the red color, and the higher the numerical value, the stronger the green color. Moreover, b value is a scale which shows yellowishness, and it means that yellow becomes strong, so that a numerical value is high, and blue becomes strong, so that a numerical value becomes high negatively.

(7) Surface resistivity Based on JIS-K7194, it measured by the 4-terminal method using the surface resistance meter (the Mitsubishi Yuka make, Lotest AMCP-T400).

(8) Adhesive force An ionomer film having a thickness of 40 μm was laminated to a polyethylene terephthalate film having a thickness of 75 μm by using a polyester adhesive to prepare a laminate for measuring an adhesive force. The ionomer surface of this laminate for measuring adhesive force and the protective layer (c) prepared on the transparent conductive thin film surface of the transparent conductive film were opposed to each other and heat sealed at 130 ° C. The laminate was peeled from the laminate for measuring adhesive force and the transparent conductive film by a 180 ° peeling method, and this peeling force was defined as the adhesive force. The peeling speed at this time was 1000 mm / min.

(9) Environmental resistance The electromagnetic wave shielding film was subjected to an endurance test under the following two conditions of moisture and heat resistance.
(I) Standing for 1000 hours in an environment of 60 ° C. and 90% RH (ii) Standing for 1000 hours in an environment of 80 ° C. and 60% RH The number of optical defects that can be visually observed was evaluated according to the following criteria. This evaluation relates to durability, that is, to evaluate the visibility after long-term storage under high temperature and high humidity.
○: No defects that can be visually observed are found Δ: Less than 3 defects that can be visually observed ×: 3 or more defects that can be visually observed

Example 1
In order to expose a biaxially oriented transparent PET film having an easy-adhesion layer on one side (A4140, manufactured by Toyobo Co., Ltd., thickness: 125 μm) in a vacuum chamber, a rewinding process was performed. The pressure at this time was 0.002 Pa, and the exposure time was 20 minutes. The surface temperature of the center roll was 40 ° C.

Next, a transparent conductive thin film made of indium-tin composite oxide was formed on the surface of the PET film having the easy adhesion layer. At this time, the pressure before sputtering was set to 0.001 Pa, and indium oxide containing 10% by mass of tin oxide as a target (Mitsui Metal Mining Co., Ltd., density 7.1 g / cm ³ ) was used, and 2 W / cm ^2. DC power was applied. Further, Ar gas was flowed at 130 sccm and O ₂ gas was flowed at 10 sccm, and a film was formed by DC magnetron sputtering in an atmosphere of 0.4 Pa. However, in order to prevent arc discharge instead of normal DC, a pulse with a width of 5 μs was applied at a frequency of 50 kHz using an RPG-100 manufactured by Nippon NI. Moreover, the surface temperature of the center roll was controlled at 50 ° C. to perform sputtering.

  In addition, while constantly monitoring the oxygen partial pressure of the atmosphere with a sputter process monitor (manufactured by Hakuto, SPM200), an oxygen gas flow meter and a DC power source are used so that the degree of oxidation in the indium-tin composite oxide thin film becomes constant. I'm back. As described above, a transparent conductive thin film made of an indium-tin composite oxide having a thickness of 22 nm was deposited.

  Furthermore, copolymer polyester resin (Toyobo Co., Ltd., Byron RV280; ionic group amount 120 eq / ton) 2.5 parts by mass and isocyanate-based crosslinking agent (Nihon Polyurethane Industry Co., Ltd. Coronate L) 2.0 parts by mass As a part and a solvent, 67.0 parts by mass of methyl ethyl ketone and 28.5 parts by mass of toluene were mixed to prepare a coating solution for forming a protective layer (C). Next, the coating liquid for forming the protective layer (C) prepared above was coated on the transparent conductive thin film using a bar coating method. The wire bar used was No. 10. Next, heat treatment was performed at 150 ° C. for 2 minutes to produce an electromagnetic wave shielding film. The protective layer (C) had a refractive index of 1.55 and a thickness of 0.1 μm.

Comparative Example 2
In Example 1, as a resin used for the protective layer (C), a copolymerized polyester resin having no ionic group (Toyobo Co., Ltd., Byron RV200; ionic group amount 0 eq / ton) was used. In the same manner as in Example 1, an electromagnetic wave shielding film was produced.

Comparative Example 3
In Example 1, as the protective layer (C), an electromagnetic wave was formed in the same manner as in Example 1 except that a layer made of a fluororesin (made by JSR, JN7212; refractive index 1.40) having a film thickness of 0.1 μm was used. A shield film was produced.

Comparative Example 4
In Example 1, the protective layer (C) is the same as Example 1 except that a layer made of a polysiloxane polymer having a film thickness of 0.1 μm (Colcoat, Colcoat P; refractive index 1.45) is used. Thus, an electromagnetic wave shielding film was prepared.

Example 2
Using the electromagnetic wave shielding film obtained in Example 1, on the surface opposite to the surface provided with the transparent conductive layer (B) and the protective layer (C), a fluororesin (made by JSR) having a thickness of 0.1 μm is further provided. , JN7212; refractive index 1.40).

Comparative Example 1
An electromagnetic wave shielding film was prepared in the same manner as in Example 1 except that the protective layer (C) was not provided.

In Example 1 and 2 , the light transmittance at a wavelength of 550 nm is obtained by providing the transparent conductive layer (B) on one side of the transparent polymer film (A) and further providing the protective layer (C) on the transparent conductive layer. However, both of them were excellent in transparency of 90% or more, and an electromagnetic wave shielding film having excellent visibility when incorporated in a liquid crystal display was obtained.

  In particular, the electromagnetic wave shielding films of Examples 1 and 5 have an excellent adhesion force to the transparent conductive layer due to the provision of the protective layer (C) containing an ionic group. Excellent visibility can be maintained even when used for a long time under humidity.

  Moreover, the electromagnetic wave shielding film of Example 5 is more transparent than the transparent polymer film (A) on the surface opposite to the surface of the transparent polymer film (A) on which the transparent conductive layer (B) and the protective layer (C) are laminated. Furthermore, since it was the structure which provided the layer (D) with a low refractive index, it was further excellent in transparency.

  In Comparative Example 1, since there was no protective layer (C), the transmittance at 550 nm was low, and good visibility was not obtained when it was incorporated in a liquid crystal display panel due to the coloring property of ITO.

  The electromagnetic shielding film of the present invention has high light transmittance, very little coloration, and good electromagnetic shielding properties. Therefore, when used as a liquid crystal display panel member, the electromagnetic shielding film is an electron by electromagnetic waves without reducing visibility. The malfunction of the apparatus can be prevented, and it is extremely useful particularly for a large-sized liquid crystal display panel of 20 inches or more.

Claims (2)

A transparent polymer film (A), a transparent conductive layer (B), and a polyester resin into which an ionic group is introduced are cross-linked with a cross-linking agent, and the ionic group concentration is 20 to 1000 eq / ton and is cross-linked It is composed of a resin having a structure, and a protective layer (C) having a refractive index of 1.40 to 1.70 is laminated in this order, and the light transmittance at a wavelength of 550 nm is 90% or more. An electromagnetic shielding film characterized by. A layer (D) having a refractive index lower than that of the transparent polymer film (A) is provided on the opposite surface of the transparent polymer film (A) from the surface on which the transparent conductive layer (B) and the protective layer (C) are laminated. The electromagnetic wave shielding film according to claim 1 , wherein the electromagnetic wave shielding film is provided.