JP6617561B2 - Laminated polyester film and polarizing plate using the same - Google Patents

Description

  The present invention relates to a polyester film used for optical applications, and more particularly to a polyester film used suitably for polarizer protection applications. Since it has a laminated structure having a polyester A layer and a polyester B layer having a melting point lower than that of the polyester A layer, the retardation (Re) with respect to the center and the direction perpendicular to the film surface at a width of 400 mm is 1000 nm or less. The present invention relates to a polyester film that does not exhibit an interference color when used for polarizer protection and the like, and a polarizing plate.

  Thermoplastic resin films, especially biaxially stretched polyester films, have excellent properties such as mechanical properties, electrical properties, dimensional stability, transparency, and chemical resistance. Widely used as a substrate film in applications. In particular, in recent years, in the flat panel display and touch panel fields, demand for various optical films such as a polarizer protective film and a transparent conductive film is increasing. Among them, in the use of a polarizer protective film, replacement of a conventional TAC (triacetyl cellulose) film with a biaxially stretched polyester film has been actively studied for the purpose of cost reduction.

  However, in the biaxially stretched polyester film that has been studied conventionally, the retardation is higher than that of the TAC film due to the orientation of the polymer at the time of stretching. Therefore, when assembled as a liquid crystal display, the interference color due to the retardation is As a result, there is a problem that the quality when displaying an image is lowered. In order to solve this problem, methods for controlling retardation have been proposed (for example, Patent Document 1 and Patent Document 2).

JP 2013-200355 A JP 2013-210598 A

  However, the techniques proposed in Patent Documents 1 and 2 do not control the retardation in the film width direction, and when mounted on a display device such as a large-screen liquid crystal display, the interference color in the film width direction. This is not practical for the use of a polarizer protective film.

  Then, in this invention, it aims at providing the polyester film which eliminates said fault and does not exhibit interference color, when it is used for a touch panel use, a polarizer protection use, etc., while being a biaxially stretched polyester film. .

The present invention has the following configuration.
[1] A laminated polyester film of 10 layers or less having a polyester A layer and a polyester B layer having a lower melting point than the polyester A layer,
A laminated polyester film in which the retardation (Re) with respect to the center in the width direction of the laminated film and the direction perpendicular to the film surface at a width of 400 mm is 1000 nm or less.
[2] The laminated polyester film according to [1], wherein the retardation (Re · C) at the center in the width direction of the laminated film and the retardation (Re · E) at a width of 400 mm satisfy the following formula (I).
Re · E / Re · C ≦ 1.5 (I)
[3] The laminated polyester film according to [1] or [2], wherein the film haze difference (Δ haze) before and after holding the film for 400 hours under the conditions of a temperature of 60 ° C. and a humidity of 95% is less than 1%. .
[4] The laminated polyester film according to any one of [1] to [3], in which the retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface is 2000 nm or less at the center in the width direction of the laminated film.
[5] At the center in the width direction of the laminated film, the retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface is 2000 nm or less,
When the arbitrary one direction in the film plane is the direction X and the direction orthogonal to the direction X is the direction Y, the storage elastic modulus in the film direction X and the direction Y at 95 ° C. is 800 MPa or more [1] to [4], respectively. The laminated polyester film according to any one of the above.
[6] An average value of the refractive indexes of the polyester B layer in the X, Y, and Z directions when an arbitrary direction in the film plane is the direction X, the direction perpendicular to the direction X is the direction Y, and the film thickness direction is the direction Z. The laminated polyester film according to any one of [1] to [5], wherein is 1.51 or more and 1.57 or less.
[7] The laminated polyester film according to [6], wherein the thermal shrinkage at 85 ° C. in the direction X is 0.5% or less.
[8] The laminated polyester film according to [6] or [7], wherein the heat shrinkage rate at 85 ° C. in the direction Y is 0.5% or less.
[9] The laminated polyester film according to any one of [1] to [8], wherein the polyester A layer is located in at least one outermost layer, and the plane orientation coefficient of the A layer is less than 0.16.
[10] The laminated polyester film according to any one of [1] to [9], wherein the polyester A layer is located in at least one outermost layer, and the plane orientation coefficient of the A layer is larger than 0.11.
[11] The laminated polyester film according to any one of [1] to [10], which has a three-layer configuration of A layer / B layer / A layer.
[12] The laminated polyester film according to any one of [1] to [11], wherein the thickness of each A layer is less than 3.2 μm.
[13] The polyester B layer has a structural unit derived from ethylene glycol of 60 mol% or more and 90 mol% or less and a structural unit derived from other diol of more than 10 mol% and 40 mol relative to the structural unit derived from diol. % Of the laminated polyester film according to any one of [1] to [12].
[14] The polyester B layer has a structural unit derived from terephthalic acid of 60 mol% or more and 90 mol% or less with respect to the structural unit derived from dicarboxylic acid, and the structural unit derived from other dicarboxylic acid exceeds 10 mol%, The laminated polyester film according to any one of [1] to [13], which is contained in an amount of 40 mol% or less.
[15] Retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface at the center in the width direction of the laminated film is 2000 nm or less, and any one direction in the film surface is orthogonal to direction X and direction X. When the direction is the direction Y and the film thickness direction is the direction Z, the average value of the refractive index in the X, Y and Z directions of the polyester B layer is 1.51 or more and 1.57 or less, and A layer / B layer / A layer The laminated polyester film according to [1], which has a three-layer structure.
[16] At least one selected from the group consisting of hard coat properties, self-repairing properties, antiglare properties, antireflection properties, low reflection properties, and antistatic properties on at least one outermost surface of the laminated polyester film The laminated polyester film according to any one of [1] to [15], wherein layers exhibiting a function are laminated [17] A polarizing plate having a polarizer protective film on both sides of a polarizer And the polarizing plate whose polarizer protective film used for at least one surface is the laminated polyester film in any one of [1]-[16].

  The laminated polyester film of the present invention has the effect of being able to display with high quality even when mounted on a display device such as a liquid crystal display.

It is the figure used for the measurement of retardation, Comprising: It is the figure which showed the film with a width of 400 mm. It is the figure used for the measurement of retardation, Comprising: It is the figure which showed the film with a width of 1000 mm. It is the figure used for the measurement of retardation, Comprising: It is the figure which showed the film with a 1500 mm width.

(Laminated polyester film)
Hereinafter, the laminated polyester film of the present invention will be described in detail.

  In the present invention, the laminated polyester film is a laminated polyester film of 10 layers or less having a polyester A layer and a polyester B layer having a lower melting point than the polyester A layer, and the polyester B layer needs to have a lower melting point than the polyester A layer. It is. By having the polyester B layer having a melting point lower than that of the polyester A layer, the orientation of the polyester B layer can be easily relaxed in the heat treatment step during film formation, and the retardation can be controlled to be low. The melting point in the present invention is an endothermic peak temperature that is manifested by a melting phenomenon when measured with a differential scanning calorimeter (DSC) at a heating rate of 20 ° C./min. When polyester resins having different compositions are blended and used as a film, a plurality of endothermic peaks accompanying melting may appear. In such a case, the temperature at which the absolute value of the heat flow is the largest is taken as the melting point. In addition, since the polyester B layer in the present invention is intended to relax the orientation in a heat treatment step or the like during film formation and control the retardation to be low, the polyester B layer has low crystallinity and does not have a clear melting point. If the polyester B layer does not show a clear melting point, it is considered to be lower than the melting point of the A layer.

  The laminated polyester film of the present invention has a polyester A layer and a polyester B layer having a melting point lower than that of the polyester A layer, and is not particularly limited as long as it is a laminated polyester film of 10 layers or less, and may have other layers. However, from the viewpoint of film forming properties and interlayer adhesion, a configuration in which the polyester A layer and the polyester B layer are alternately laminated is preferable, and it is preferable that the polyester A layer and the polyester B layer are only included.

  The number of layers in the laminated polyester film of the present invention needs to be 10 or less. When the number of layers to be laminated is more than 10, the thickness of each layer becomes thin, so that the lamination property at the time of film formation is lowered, a flow mark or the like is generated, and the film quality may be lowered. The laminated polyester film has 5 to 9 layers to be laminated in order to have more polyester A layers, especially when it is necessary to achieve both high dimensional stability while maintaining low retardation. It is preferable that On the other hand, when it is desired to suppress the manufacturing cost while achieving low retardation, the number of layers to be stacked is preferably 2 or more and less than 5 layers.

  The laminated polyester film of the present invention has a retardation (Re) of 1000 nm or less with respect to the width direction center of the laminated film (hereinafter, sometimes simply referred to as “center”) and the direction perpendicular to the film surface at 400 mm width. It is necessary to be. That is, in this invention, the retardation (Re) with respect to the direction perpendicular | vertical to the film surface in the width direction center of a laminated film is 1000 nm or less, and the retardation (Re) with respect to the direction perpendicular | vertical to the film surface in 400 mm width is 1000 nm or less. There must be.

  In the present invention, the retardation (Re) with respect to the direction perpendicular to the film surface is calculated from the product of the maximum value of the refractive index difference between the two orthogonal directions in the plane of the film and the film thickness. Is a measuring device sold by Oji Scientific Instruments Co., Ltd., and is a value measured by a phase difference measuring device KOBRA series that measures retardation using an optical technique. Specifically, it is a value measured at an incident angle of 0 ° (direction perpendicular to the film surface) by setting the film width direction to an angle of 0 ° defined by the measurement device.

  The 400 mm width in the present invention refers to a film having a width of 200 mm in each of two directions along the width direction from the center in the width direction of the film (FIG. 1).

  That is, the evaluation of retardation (Re) with respect to the center and the direction perpendicular to the film surface at a width of 400 mm is performed at the center in the film width direction and at a position taken at 200 mm width in two directions along the width direction from the center. (Measurement is performed with a sample cut in a 35 mm × 35 mm square from a 165 mm width position in each of two directions along the width direction from the center in the film width direction). If the film width direction in the present invention is a laminated film on a roll, the roll winding direction is the film longitudinal direction, the roll width direction is the film width direction, and the film has a cut sheet shape. The retardation (Re) is measured at the film edge in the direction perpendicular to the long side direction of the film (measured with a sample cut into a 35 mm × 35 mm square centered on the 35 mm position from the film end), and the film center The direction in which the difference is large is defined as the film width direction.

  In general, when a polyester film is used for protecting a polarizer, when the retardation (Re) value is increased when the polyester film is bonded to the polarizer, an interference color is generated when mounted on a liquid crystal display, and the quality is lowered. Therefore, it becomes a problem. In a biaxially stretched polyester film, stretching in a biaxial direction perpendicular to the production is carried out. In the stretching process, variation in retardation (Re) occurs in the plane of the film. More specifically, in sequential biaxial stretching that is generally used for biaxially stretched films, stretching in the film longitudinal direction is followed by stretching in the film width direction, and in some cases, heat treatment is then performed. However, particularly when stretching in the film width direction, a difference in retardation (Re) occurs in the film width direction due to variations in stress between the film longitudinal direction and the film width direction. Therefore, it is generally known that even when retardation (Re) is suppressed at the center in the film width direction, the retardation (Re) increases as it approaches the end when viewed in the film width direction. In this way, variation in retardation (Re) in the film width direction occurs, and in particular, when used as a protective film for a polarizer for a large display of 32 inches or more, retardation (Re) in a plane as a polarizing plate. ) Variation, and when mounted on a display device such as a liquid crystal display, it causes coloration at a high retardation (Re) region. The laminated polyester film of the present invention needs to have a film width of 400 mm or more, more preferably 1000 mm or more, and most preferably 1500 mm or more from the viewpoint of mountability for large displays.

  For the reasons described above, when the laminated polyester film of the present invention has a width of 1000 mm or more, the retardation (Re) in the direction perpendicular to the film surface at 1000 mm width is preferably 1000 nm or less, and the film width is 1500 mm width or more. In some cases, the retardation (Re) in the direction perpendicular to the film surface at a width of 1500 mm is preferably 1000 nm or less. Here, the definition of the 1000 mm width and the 1500 mm width of the present invention is the same as the 400 mm width, respectively, from the center in the width direction of the film, respectively, in the two directions along the width direction. From the center in the width direction of the film, measured in a 35 mm × 35 mm square from a 465 mm width position in each of the two directions along the width direction), a film having a width of 750 mm (measured from the center in the width direction of the film in the width direction) Measured with a sample cut in a 35 mm × 35 mm square from a 715 mm width position in each of two directions. That is, the evaluation of retardation (Re) with respect to the direction perpendicular to the film surface at a width of 1000 mm and a width of 1500 mm, respectively, is a position taken at a width of 500 mm in each of two directions along the width direction from the center of the film width direction, 750 mm It implements in the position taken in width (refer to Drawing 2 and Drawing 3).

  In order that the laminated polyester film of the present invention suppresses the generation of interference colors when mounted on a liquid crystal display, the retardation of the center and the direction perpendicular to the film surface at 400 mm width (Re) is less than 750 nm. Preferably, it is more preferably 500 nm or less, and most preferably 1 nm or more and 200 nm or less.

  Although it does not specifically limit as a technique of suppressing retardation (Re) as mentioned above, It is set as the laminated film of 10 or less layers which have the polyester A layer and the polyester B layer whose melting | fusing point is lower than the polyester A layer, The orientation of the polyester B layer is set. And a method of relaxing. The laminated polyester film of the present invention is preferably a biaxially oriented polyester film from the viewpoints of heat resistance, dimensional stability, and handleability. And as a method of relieving the orientation of the polyester B layer with the biaxially oriented polyester film, a method of increasing the stretching temperature of the film and further increasing the heat treatment temperature after biaxial stretching is preferred. A biaxially oriented polyester film is a sequential biaxial stretching method in which an unstretched film is stretched in the longitudinal direction and then stretched in the width direction, or stretched in the width direction and then stretched in the longitudinal direction. Stretching can be performed by a simultaneous biaxial stretching method or the like in which the directions are stretched almost simultaneously, but by increasing the stretching temperature, the film becomes difficult to be oriented. Specifically, the stretching temperature in the longitudinal direction is preferably 95 ° C. or higher and 130 ° C. or lower, and more preferably 100 ° C. or higher and 120 ° C. or lower. The stretching temperature in the width direction is preferably 100 ° C. or higher and 150 ° C. or lower.

  Further, the heat treatment temperature after biaxial stretching is preferably performed at a temperature of [(melting point of polyester B layer) −10 ° C.] or more and [(melting point of polyester B layer) + 30 ° C.] or less. By performing the heat treatment in the above temperature range, the orientation of the polyester B layer is relaxed, and the retardation (Re) can be controlled to be low.

  Further, as a method for controlling the retardation (Re) to be low, it is preferable to make the stretching orientation in the longitudinal direction and the width direction during biaxial stretching as isotropic as possible, for example, the stretching ratio in the longitudinal direction and the stretching in the width direction. A method in which the magnification is the same is preferably used.

  In the laminated polyester film of the present invention, the retardation (Re · C) at the center of the film and the retardation (Re · E) at a width of 400 mm preferably satisfy the following formula (I).

  Re · E / Re · C ≦ 1.5 (I)

  Satisfaction of the formula (I) indicates that variation in retardation (Re) in the film width direction is small, and when mounted on a liquid crystal display, coloring and a decrease in luminance associated with a viewing angle can be suppressed. More preferably, the expression (I ′) is satisfied, and the expression (I ″) is most preferable.

Re · E / Re · C ≦ 1.4 (I ')
0.8 ≦ Re · E / Re · C ≦ 1.3 (I ″).

  As a method of satisfying the formula (I), it is preferable that the difference between the orientation angles in the center of the laminated film width direction and the width of 400 mm is 20 ° or less. The orientation angle here refers to the direction in which the refractive index on the film is the largest, and is actually measured by an optical method in the same manner as retardation. As a method of setting the difference between the orientation angles in the width direction of the laminated film and the width of 400 mm to 20 ° or less, a method in which stretching in the width direction is divided into a plurality of zones and gradually increasing in temperature is preferable. The temperature is set to 100 ° C. or more and 120 ° C. or less, the stretching middle temperature is set to 105 ° C. or more and 130 ° C. or less, the stretching latter half temperature is set to 110 ° C. or more and 150 ° C. or less. The way to go is mentioned.

  The laminated polyester film of the present invention preferably has a film haze difference (Δhaze) before and after holding the film for 400 hours under a temperature of 60 ° C. and a humidity of 95% of less than 1%. By maintaining the Δhaze when held for a long time at a high temperature and high humidity as low as less than 1% as described above, the appearance changes even when the polarizing plate using the film of the present invention is exposed to a high temperature and high humidity. It becomes possible to suppress. As a method of setting the film haze difference (Δ haze) before and after holding the film for 400 hours under the conditions of a temperature of 60 ° C. and a humidity of 95% to less than 1%, the amount of cyclic trimer in the polyester film Is 100% by mass or less, preferably 1% by mass or less, more preferably 0.9% by mass or less, and still more preferably 0.85% by mass or less. The lower limit of haze is not particularly limited, but the practical lower limit is 0%.

The laminated polyester film of the present invention preferably has a retardation (R50 °) of 2000 nm or less with respect to an angle inclined by 50 ° with respect to the film surface at the center of the film. Here, the retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface is a measurement sold by Oji Scientific Instruments Co., Ltd., similarly to the retardation (Re) with respect to the direction perpendicular to the film surface described above. It is a value of retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface, using a value measured by a phase difference measuring device KOBRA series that measures retardation with an optical technique. .
By controlling the retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface as low as 2000 nm or less, when viewing a liquid crystal display equipped with a polarizing plate using the film of the present invention, A decrease in luminance can be suppressed with high accuracy. The retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface is further preferably 1500 nm or less, and most preferably 1 nm or more and 1000 nm or less.

  As a method of setting the retardation (R50 °) for an angle inclined by 50 ° with respect to the film surface to 2000 nm or less, any one direction in the film surface is the direction X, the direction orthogonal to the direction X is the direction Y, and the film thickness direction. Is the direction Z, it is preferable to make the difference between the average value of the X and Y refractive indices of the polyester B layer and the refractive index in the Z direction as small as possible. The laminated polyester film of the present invention is preferably biaxially oriented, but when it is biaxially oriented, the in-plane refractive index is significantly greater than the refractive index in the film thickness direction. For this reason, it is important to lower the refractive index in the film plane while maintaining biaxial orientation. As a method for lowering the refractive index in the film plane, the polyester B layer has a structural unit derived from ethylene glycol of 60 mol% or more and 90 mol% or less of the structural unit derived from diol, and a structural unit derived from other diol. In a composition containing more than 10 mol% and 40 mol% or less, and the polyester B layer has a structural unit derived from terephthalic acid of 60 mol% or more and 90 mol% or less with respect to the structural unit derived from dicarboxylic acid. And a method in which other dicarboxylic acid-derived structural units are contained in an amount exceeding 10 mol% and not more than 40 mol%. The structural unit derived from ethylene glycol is preferably less than 90 mol%. Moreover, it is preferable that the structural unit derived from terephthalic acid is less than 90 mol%.

  By containing more than 10 mol% of structural units derived from diols other than structural units derived from ethylene glycol with respect to the structural units derived from diol in the polyester B layer, the refractive index within the film plane during biaxial orientation can be obtained. It becomes easy to control low. Similarly, by containing more than 10 mol% of a structural unit derived from a dicarboxylic acid other than a structural unit derived from terephthalic acid with respect to a structural unit derived from a dicarboxylic acid of the polyester B layer, the film surface during biaxial orientation It becomes easy to control the refractive index inside.

  Here, as the structural unit derived from diol other than the structural unit derived from ethylene glycol, for example, 1,2-propanediol, 1,3-propanediol, neopentyl glycol, 1,3-butanediol, 1,4- Butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,2-cyclohexanedimethanol, 1,3-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, diethylene glycol, triethylene glycol, polyalkylene glycol, 2,2-bis (4-hydroxyethoxyphenyl) propane, isosorbate, spiroglycol and the like can be mentioned. Among these, neopentyl glycol, diethylene glycol, 1,4-cyclohexanedimethanol, isosorbate, and spiro glycol are preferably used. These diol-derived structural units may be used alone or in combination of two or more in addition to the ethylene glycol-derived structural unit.

  Examples of the structural unit derived from dicarboxylic acid other than the structural unit derived from terephthalic acid include, for example, isophthalic acid, phthalic acid, 1,4-naphthalenedicarboxylic acid, 1,5-naphthalenedicarboxylic acid, and 2,6-naphthalenedicarboxylic acid. Structural units derived from aromatic dicarboxylic acids such as 4,4'-diphenyldicarboxylic acid, 4,4'-diphenyletherdicarboxylic acid, 4,4'-diphenylsulfonedicarboxylic acid, adipic acid, suberic acid, sebacic acid, dimer acid , Structural units derived from aliphatic dicarboxylic acids such as dodecanedioic acid and cyclohexanedicarboxylic acid, and ester derivatives thereof. Of these, isophthalic acid, 2,6-naphthalenedicarboxylic acid, and cyclohexanedicarboxylic acid are preferably used. In addition to the structural unit derived from terephthalic acid, these structural units derived from dicarboxylic acid may be used alone or in combination of two or more, and some oxyacids such as hydroxybenzoic acid may be partially used together. Polymerization may be performed.

  In addition, the laminated polyester film of the present invention has a retardation with respect to an angle inclined by 50 ° with respect to the film surface at the center of the film in order to achieve both high accuracy suppression of coloration and luminance reduction depending on the viewing angle and heat resistance. R50 °) is 2000 nm or less, and when the arbitrary direction in the film plane is the direction X and the direction orthogonal to the direction X is the direction Y, the storage elastic modulus in the film direction X and the direction Y at 95 ° C. is respectively , 800 MPa or more is preferable. By setting the storage elastic modulus in the film direction X and the direction Y at 95 ° C. to 800 MPa or more, dimensional stability in processing steps such as vapor deposition, coating, and lamination can be maintained. From the viewpoint of heat resistance to the laminated polyester film of the present invention, the storage elastic modulus in the film direction X and the direction Y at 95 ° C. is more preferably 850 MPa or more, and most preferably 900 MPa or more.

  When watching a liquid crystal display equipped with a polarizing plate using the laminated polyester film of the present invention, in order to suppress the coloration and brightness reduction due to the viewing angle with high accuracy, and at the same time to maintain the dimensional stability in the processing process, The retardation (R50 °) for an angle inclined by 50 ° C. with respect to the film surface is preferably 1 nm or more and 1000 nm or less, and the storage elastic modulus in the film direction X and direction Y at 95 ° C. is 900 MPa or more and 5000 MPa or less. Most preferred.

  In the center of the laminated polyester film of the present invention, the retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface is 2000 nm, and the storage elastic modulus in the direction X and direction Y at 95 ° C is 800 MPa, respectively. As a method for the above, the intrinsic viscosity of the resin used for the polyester B layer is preferably 0.7 or more, and the composition of the B layer is a structure derived from ethylene glycol with respect to a structural unit derived from diol. The unit is 75 mol% or more and less than 90 mol%, and other diol-derived structural units are contained in an amount of 10 mol% or more and less than 25 mol%, or the polyester B layer is based on a dicarboxylic acid-derived structural unit. More than 75 mol% and less than 90 mol% of structural units derived from terephthalic acid, other dicarboxylic acid It is preferable that the conventional structural unit is contained in an amount of 10 mol% to 25 mol%. Furthermore, the heat treatment temperature after biaxial stretching is preferably performed at a temperature of [(melting point of polyester B layer) −10 ° C.] or more and [(melting point of polyester B layer) + 10 ° C.] or less.

  The resin used for the polyester A layer contains 98 mol% or more of a structural unit derived from ethylene glycol with respect to the structural unit derived from diol, and a structural unit derived from terephthalic acid relative to the structural unit derived from dicarboxylic acid. It is preferable to be 98 mol% or more.

  The laminated polyester film of the present invention has an X, Y, and Z directions of the polyester B layer, where direction X is an arbitrary direction in the film plane, direction Y is a direction orthogonal to direction X, and direction Z is a film thickness direction. The average refractive index is preferably 1.51 or more and 1.57 or less. By controlling the average value of the refractive index in the X, Y, and Z directions as low as the above range, retardation with respect to the direction perpendicular to the film surface (Re) and retardation with respect to an angle inclined by 50 ° with respect to the film surface (R50 ° Since the absolute value of) is low and easy to control, it is easy to achieve high-quality display when mounted on a display device such as a liquid crystal display, which is the object of the present invention.

  As a method of setting the average value of the refractive indexes in the X, Y, and Z directions of the polyester B layer in the above range, the structural unit derived from ethylene glycol is 65 mol% or more to 85 mol% with respect to the structural unit derived from the diol of the polyester B layer. Less than mol%, neopentyl glycol, diethylene glycol, 1,4-cyclohexanedimethanol, isosorbate, spiroglycol-containing structural unit derived from diol 15 mol% or more less than 35 mol%, polyester B layer The structural unit derived from terephthalic acid is 65 mol% or more and less than 85 mol%, and the structural unit derived from isophthalic acid, 2,6-naphthalenedicarboxylic acid or cyclohexanedicarboxylic acid is 15 mol% or more with respect to the structural unit derived from dicarboxylic acid. The method of containing less than 35 mol% is mentioned, Especially polyester B layer 65 mol% or more and less than 85 mol% of structural units derived from ethylene glycol with respect to structural units derived from diol, derived from diol selected from neopentyl glycol, diethylene glycol, 1,4-cyclohexanedimethanol, isosorbate, spiroglycol The method of containing the structural unit of 15 mol% or more and less than 35 mol% is more preferably used.

  When the laminated polyester film of the present invention is used for polarizer protection, the thermal contraction rate at 85 ° C. in any one direction X in the film plane is 0. 0 in order to reduce warpage when bonded to the polarizer. It is preferable that it is 5% or less. By setting the heat shrinkage rate at 85 ° C. in the X direction to 0.5% or less, it is possible to suppress the film from shrinking due to the heat applied to the film when being bonded to the polarizer, and to reduce the occurrence of warping of the polarizing plate. Can do. Similarly, the laminated polyester film of the present invention preferably has a thermal shrinkage rate at 85 ° C. in the direction Y orthogonal to the direction X of 0.5% or less.

  The thermal contraction rate at 85 ° C. in the X direction and the Y direction is more preferably 0.3% or less, and most preferably 0.1% or less. Furthermore, in the laminated polyester film of the invention, from the viewpoint of reducing warpage, the thermal shrinkage at 85 ° C. is very preferably from −0.5% to 0.1% from the viewpoint of handleability. As a method for setting the heat shrinkage rate at 85 ° C. in the X direction and the Y direction to 0.5% or less, it is preferable that the number of layers of the polyester A layer and the polyester B layer is 5 or more and 9 or less. Moreover, in the preheating process at the time of extending | stretching to a longitudinal direction and the width direction, it is preferable to preheat at 85 degreeC conditions for 1 second or more. In order to reduce the thermal shrinkage rate at the target temperature, it is effective to remove the distortion of the film at the target temperature in the preheating step before stretching.

  In the laminated polyester film of the present invention, it is preferable that the polyester A layer is located in at least one outermost layer, and the plane orientation coefficient of the A layer is larger than 0.11. By adopting the above-described configuration, it becomes possible to maintain the rigidity of the film at the same time while achieving low retardation, thereby improving the handleability. The plane orientation coefficient of the A layer is more preferably 0.115 or more, and most preferably 0.12 or more. Further, from the viewpoint of handleability and film formation stability, it is preferable that the polyester A layer is located in at least one outermost layer, and the plane orientation coefficient of the A layer is less than 0.16. As a method of setting the plane orientation coefficient of the A layer within the above range, the polyester A layer contains 95 mol% to 100 mol% of a structural unit derived from ethylene glycol with respect to the structural unit derived from diol, and is a dicarboxylic acid. It is preferable to contain 95 mol% or more and 100 mol% or less of a structural unit derived from terephthalic acid with respect to the acid derived structural unit.

The plane orientation coefficient is the refractive index (nX) in any one direction X in the film plane and the direction Y orthogonal to the direction X using an Abbe refractometer using sodium D line (wavelength 589 nm) as a light source. The refractive index (nY) and the refractive index (nZ) in the thickness direction Z are measured, and the plane orientation coefficient (fn) is calculated from the following formula.
fn = (nX + nY) / 2−nZ.

  In the present invention, since the polyester A layer and the polyester B layer having a melting point lower than that of the polyester A layer are provided, a plurality of refractive indexes are observed in the X direction, the Y direction, and the Z direction. For this reason, among the observed refractive indexes, in the X direction and the Y direction, the lowest value is the refractive index of the polyester B layer, the highest value is the refractive index of the polyester A layer, and the lowest value is in the Z direction. The value is the refractive index of the polyester A layer, and the highest value is the refractive index of the polyester B layer.

  The laminated polyester film of the present invention preferably has a [total layer thickness of layer A / total layer thickness of layer B] of 0.1 or more and 1 or less. The total layer thickness referred to here is obtained for layers made of the same resin by observing the laminated state using a transmission electron microscope (TEM) in a cross section cut out in the center in the width direction of the laminated film. It is the sum total of all layer thicknesses. The smaller the sum of the layer thicknesses of the A layers / the sum of the layer thicknesses of the B layers, the lower the retardation, and the easier it is to control the retardation. Therefore, the sum of the layer thicknesses of the A layers / B layer layers The total thickness is more preferably from 0.1 to 0.5, and most preferably from 0.1 to 0.3.

  The laminated film of the present invention preferably has a three-layer structure of A layer / B layer / A layer when importance is attached to the versatility of equipment.

  In addition, the retardation (Re) with respect to the direction perpendicular to the film surface is calculated from the product of the maximum value of the refractive index difference between the two directions perpendicular to each other in the plane of the film and the film thickness, so that the retardation is controlled to be low. It is preferable that the film thickness is thinner. For this reason, the laminated polyester film of the present invention has a thickness of preferably 5 μm or more and 75 μm or less, more preferably 10 μm or more and 50 μm or less, and more preferably 15 μm or more and 45 μm or less from the viewpoints of handleability and low retardation control. Is most preferable.

  In order to achieve both low retardation control and rigidity, the thickness per layer of the polyester A layer is preferably less than 3.2 μm. In order to maintain rigidity, the polyester A layer has a melting point higher than that of the polyester B layer, contains 95 mol% to 100 mol% of structural units derived from ethylene glycol with respect to the structural units derived from diol, and Since it is preferable to contain 95 mol% or more and 100 mol% or less of a structural unit derived from terephthalic acid with respect to the structural unit derived from an acid, a phase difference is likely to occur as compared with the polyester B layer. For this reason, it is preferable to reduce the thickness of the polyester A layer. The thickness per layer of the polyester A layer is more preferably 3 μm or less, and most preferably 1 μm or more and 2.8 μm or less. In addition, when the laminated polyester film of this invention has two or more polyester A layers, it is preferable that the thickness per layer of each polyester A layer shall be less than 3.2 micrometers.

  In addition, the laminated polyester film of the present invention has various additives such as antioxidants, heat stabilizers, weather stabilizers, ultraviolet absorbers, organic lubricants, pigments, dyes, organic or inorganic fine particles, fillers, Antistatic agents, nucleating agents, and the like may be added to such an extent that the characteristics are not deteriorated.

(Surface layer)
In addition to the above-mentioned problems, the laminated polyester film of the present invention has a hard coat property, a self-repairing property, an anti-proofing property on at least one outermost surface in order to impart process stability in the manufacturing process and durability in the use environment. It is preferable to have a layer exhibiting one or more functions selected from the group consisting of glare, antireflection, low reflection, ultraviolet shielding, and antistatic properties (the layer is also referred to as “surface layer”). . Among them, at least one selected from the group consisting of hard coat properties, self-healing properties, antiglare properties, antireflection properties, low reflection properties, and antistatic properties is provided on at least one outermost surface of the laminated polyester film of the present invention. It is particularly preferable that layers exhibiting the above functions are laminated.

  The thickness of the surface layer varies depending on its function, but is preferably in the range of 10 nm to 30 μm, and more preferably 50 nm to 20 μm. If it is thinner than this, the effect is insufficient, and if it is thicker, there is a possibility of adversely affecting optical performance and the like.

Here, the hard coat property is a function of making the surface hard to be damaged by increasing the hardness of the surface. As its function, it is preferably HB or higher, more preferably 2H or higher, or # 0000 steel wool as evaluated by scratch hardness (pencil method) described in JIS K5600-5-4 (1999). In the scratch resistance test (steel wool scratch resistance test) conducted under the conditions of 200 g / cm ² and 10 reciprocations, preferably 5 or less weak scratches, more preferably no scratches.

  Here, the self-repairing property is a function of making the scratch difficult by repairing the wound by elastic recovery or the like, and the function is preferably when the film surface is rubbed with a brass brush under a load of 500 g. The wound recovers within 3 minutes, more preferably within 1 minute.

  The anti-glare property is a function of improving visibility by suppressing reflection of external light by light scattering on the surface. The function is preferably 2 to 50%, more preferably 2 to 40%, particularly preferably 2 to 2% in the evaluation based on the method for obtaining haze described in JIS K7136 (2000). 30%.

  Antireflection and low reflectivity are functions that improve visibility by reducing the reflectance at the surface due to the interference effect of light. Its function is preferably 2% or less, particularly preferably 1% or less, by reflectance spectroscopy measurement. The reflectance here refers to a value at a wavelength of 550 nm.

The antistatic property is a function of removing triboelectricity generated by peeling from the surface or rubbing on the surface by leaking. As a standard of the function, the surface resistivity described in JIS K6911 (2006) is preferably 10 ¹¹ Ω / □ or less, more preferably 10 ⁹ Ω / □ or less. In addition to a layer containing a known antistatic agent, the antistatic property may be imparted from a layer containing a conductive polymer such as polythiophene, polypyrrole or polyaniline. Hereinafter, the provision of hard coat properties and antiglare properties will be described in more detail.

  The material used for the surface layer imparting the hard coat property (hereinafter, referred to as a hard coat layer) can be a material used for a known hard coat layer, and is not particularly limited, but is dry, heat, chemical reaction Alternatively, a resin compound that polymerizes and / or reacts by irradiation with any of electron beam, radiation, and ultraviolet light can be used. Examples of such a curable resin include melamine-based, acrylic-based, silicon-based, and polyvinyl alcohol-based curable resins, but acrylic resins that are cured by electron beams or ultraviolet rays in terms of obtaining high surface hardness or optical design. A curable resin is preferred.

  An acrylic resin that is cured by an electron beam or ultraviolet ray has an acrylate-based functional group. For example, a relatively low molecular weight polyester resin, polyether resin, acrylic resin, epoxy resin, urethane resin, alkyd resin, spiro resin Acetal resins, polybutadiene resins, polythiol polyene resins, oligomers or prepolymers of polyfunctional compounds such as polyhydric alcohols (meth) acrylates and prepolymers and reactive diluents such as ethyl (meth) acrylate, ethylhexyl (meth) acrylate, styrene, methyl Monofunctional monomers such as styrene and N-vinylpyrrolidone as well as polyfunctional monomers such as trimethylolpropane tri (meth) acrylate, hexanediol (meth) acrylate, tripropylene glycol di (meth) acrylate Contains rate, diethylene glycol di (meth) acrylate, pentaerythritol tri (meth) acrylate, dipentaerythritol hexa (meth) acrylate, 1,6-hexanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, etc. Things can be used.

  In the case of an electron beam or ultraviolet curable resin, as a photopolymerization initiator in the above-mentioned resin, acetophenones, benzophenones, Michler benzoylbenzoate, α-amyloxime ester, tetramethyltyramium monosulfide, thioxanthones, As a photosensitizer, n-butylamine, triethylamine, tri-n-butylphosphine and the like can be mixed and used. It is preferable that the addition amount of the said photoinitiator is 0.1-10 mass parts with respect to 100 mass parts of electron beam ultraviolet curable resins.

  Although it does not specifically limit as a hardening method of the said coating film, It is preferable to carry out by ultraviolet irradiation. When curing by ultraviolet rays, it is preferable to use ultraviolet rays having a wavelength range of 190 to 380 nm. Curing with ultraviolet rays can be performed by, for example, a metal halide lamp, a high pressure mercury lamp, a low pressure mercury lamp, an ultrahigh pressure mercury lamp, a carbon arc lamp, a black light fluorescent lamp, or the like. Specific examples of the electron beam source include various electron beam accelerators such as a cockcroft-wald type, a bandegraft type, a resonant transformer type, an insulated core transformer type, a linear type, a dynamitron type, and a high frequency type.

  Siloxane-based thermosetting resins are also useful as the resin for the hard coat layer, and can be produced by hydrolyzing and condensing the organosilane compound alone or in combination of two or more under an acid or base catalyst.

  The film thickness of the hard coat layer is preferably 0.5 μm to 20 μm, more preferably 1 μm to 20 μm, and even more preferably 1 μm to 15 μm.

  As the resin used for the surface layer imparting the antiglare property (hereinafter referred to as the antiglare layer), the same resin as the electron beam or ultraviolet curable resin described above can be used. Further, one or two or more of the above-described resins can be mixed and used. Further, in order to adjust physical properties such as plasticity and surface hardness, a resin that is not cured by an electron beam or ultraviolet rays can be mixed. Examples of resins that can be used for the antiglare layer and that are not cured by electron beams or ultraviolet rays include polyurethane, cellulose derivatives, polyesters, acrylic resins, polyvinyl butyral, polyvinyl alcohol, polyvinyl chloride, polyvinyl acetate, polycarbonate, and polyamide.

Specific examples of the particles used in the antiglare layer include, for example, particles of inorganic compounds such as silica particles, alumina particles, TiO ₂ particles, or polymethyl methacrylate particles, acrylic-styrene copolymer particles, crosslinked acrylic particles, melamine particles. Preferred are resin particles such as crosslinked melamine particles, polycarbonate particles, polyvinyl chloride particles, benzoguanamine particles, crosslinked benzoguanamine particles, polystyrene particles, and crosslinked polystyrene particles. As the shape, spherical particles having a uniform surface protrusion shape are preferably used, but indefinite shapes such as layered inorganic compounds such as talc and bentonite can also be used. Two or more different kinds of particles may be used in combination. Even if there are two or more kinds of material, two or more kinds of particles having different particle size distributions may be used, and there is no limitation.

  The particle size of the particles used in the antiglare layer is 0.5 to 10 μm, more preferably 0.5 to 5 μm, further preferably 0.5 to 3 μm, and still more preferably 0.5 to 1.5 μm. Moreover, content of the said particle | grain is 1-50 mass% with respect to resin which comprises an anti-glare layer, and 2-30 mass% is more preferable.

  The film thickness of the antiglare layer is preferably 0.5 μm to 20 μm, more preferably 1 μm to 20 μm, and further preferably 1 μm to 10 μm.

  As the antiglare layer used in the present invention, JP-A-6-18706, JP-A-10-20103, JP-A-2009-227735, JP-A-2009-86361, JP-A-2009-80256 are disclosed. JP, 2011-81217, JP 2010-204479, JP 2010-181898, JP 2011-197329, JP 2011-197330, JP 2011-215393, etc. The described antiglare layer can also be suitably used.

  In addition to the components described above, the surface layer may contain other components as necessary within a range not losing the effects of the invention. Other components include, but are not limited to, for example, inorganic or organic pigments, polymers, polymerization initiators, polymerization inhibitors, antioxidants, dispersants, surfactants, light stabilizers, leveling agents, An antistatic agent, an ultraviolet absorber, a catalyst, an infrared absorber, a flame retardant, an antifoaming agent, conductive fine particles, a conductive resin, and the like can be added.

(Polarizer protection, polarizing plate)
The laminated film of the present invention is preferably used for polarizer protection. Moreover, the polarizing plate of the present invention is a polarizing plate having a polarizer protective film on one side or both sides of the polarizer, and the polarizer protective film on at least one side is the laminated polyester film. preferable. The polarizer protective film used on the other surface of the polarizer may be the laminated polyester film of the present invention, or a film having no birefringence as typified by a triacetyl cellulose film, an acrylic film, or a norbornene film. It is also preferable to use.

  Examples of the polarizer include a polyvinyl alcohol film containing a dichroic material such as iodine. The polarizer protective film is bonded to the polarizer directly or via an adhesive layer, but is preferably bonded via an adhesive from the viewpoint of improving adhesiveness. As a preferable polarizer for bonding the polyester film of the present invention, for example, iodine or dichroic material is dyed and adsorbed on a polyvinyl alcohol film, uniaxially stretched in a boric acid aqueous solution, and the stretched state is maintained. The polarizer obtained by performing washing | cleaning and drying is mentioned. The draw ratio of uniaxial stretching is usually about 4 to 8 times. Polyvinyl alcohol is suitable as the polyvinyl alcohol film. “Kuraray Vinylon” [manufactured by Kuraray Co., Ltd.], “Tosero Vinylon” [manufactured by Toh Cello Co., Ltd.], “Nichigo Vinylon” [Nippon Synthetic Chemical Co., Ltd.] Commercial products such as “made” can be used. Examples of the dichroic material include iodine, a disazo compound, and a polymethine dye. Since the laminated film of the present invention controls the retardation to be low in the width direction, it does not exhibit an interference color when mounted on a display device such as a large-screen liquid crystal display and is preferably used.

(Touch panel use)
The laminated film of the present invention is also suitably used for touch panel applications. Specifically, it is suitably used for applications in which a conductive layer such as a hard coat layer or indium tin oxide (hereinafter referred to as ITO) is provided on the laminated film of the present invention.

(Production method)
Next, the preferable manufacturing method of the film of this invention is demonstrated with a specific example below. However, the present invention is not construed as being limited to such examples.

  Polyester A used for the polyester A layer and polyester B used for the polyester B layer having a melting point lower than that of the polyester A layer are respectively fed to separate vent type twin screw extruders and melt extruded. At this time, it is preferable to control the resin temperature to 265 ° C. to 295 ° C. under an atmosphere of flowing nitrogen in the extruder, with an oxygen concentration of 0.7% by volume or less. Next, foreign matter is removed and the amount of extrusion is leveled through a filter and a gear pump, respectively, and discharged from the T die onto a cooling drum in a sheet form. At that time, an electrostatic application method in which the cooling drum and the resin are brought into close contact with each other by static electricity using an electrode applied with a high voltage, a casting method in which a water film is provided between the casting drum and the extruded polymer sheet, and the casting drum temperature is set to [polyester resin]. Glass transition point (glass transition temperature)] to [(glass transition temperature of polyester resin) -20 ° C.], or a method of adhering the extruded polymer, or a method combining a plurality of these methods, The film is brought into close contact with the casting drum and cooled and solidified to obtain an unstretched film. Among these casting methods, when using polyester, a method of applying an electrostatic force is preferably used from the viewpoint of productivity and flatness.

  The polyester film of the present invention is preferably a biaxially oriented film from the viewpoint of heat resistance and dimensional stability. The biaxially oriented film is obtained by stretching an unstretched film in the longitudinal direction and then stretching in the width direction, or by stretching in the width direction and then stretching in the longitudinal direction, or by the longitudinal direction of the film. It can be obtained by stretching by a simultaneous biaxial stretching method in which the width direction is stretched almost simultaneously.

  As the draw ratio in such a drawing method, preferably 2.8 times or more and 3.5 times or less, more preferably 3 times or more and 3.3 times or less in the longitudinal direction. The stretching speed is preferably 1,000% / min or more and 200,000% / min or less. The stretching temperature in the longitudinal direction is preferably 95 ° C. or higher and 130 ° C. or lower, and it is preferable to preheat at 85 ° C. for 1 second or longer before stretching. Further, the stretching ratio in the width direction is preferably 2.8 times or more and 3.5 times or less, more preferably 3 times or more and 3.5 times or less, and it is preferable to match the stretching ratio in the longitudinal direction. The stretching speed in the width direction is desirably 1,000% / min or more and 200,000% / min or less. Further, in order to reduce the variation in retardation (Re) at the center of the film and retardation (Re) in the width of 400 mm, the first half temperature of stretching is 100 ° C. or more and 120 ° C. or less, the middle temperature of stretching is 105 ° C. or more and 130 ° C. or less and further stretching The latter half temperature is preferably set to 110 ° C. or higher and 150 ° C. or lower, and preheated at 85 ° C. for 1 second or longer before stretching.

  Furthermore, the film is heat-treated after biaxial stretching. The heat treatment can be performed by any conventionally known method such as in an oven or on a heated roll. This heat treatment is performed at a temperature of 120 ° C. or higher and lower than the crystal melting peak temperature of the polyester, preferably, [(melting point of the polyester B layer) −10 ° C.] or higher and [(melting point of the polyester B layer) + 30 ° C.] or lower. is there. Here, the preferable heat treatment temperature indicates the highest temperature among the heat treatment temperatures performed after biaxial stretching. The heat treatment time can be arbitrarily set within a range not deteriorating the characteristics, and is preferably 5 seconds to 60 seconds, more preferably 10 seconds to 40 seconds, and most preferably 15 seconds to 30 seconds. Good.

  Furthermore, in order to improve the adhesive force with the polarizer, at least one surface can be subjected to corona treatment or an easy-adhesion layer can be coated. As a method of providing the coating layer in-line in the film manufacturing process, a coating layer composition dispersed in water on a film that has been at least uniaxially stretched is uniformly using a metalling ring bar or gravure roll. A method of drying the coating agent while applying it to the coating layer is preferable. In this case, the thickness of the easy-adhesion layer is preferably 0.01 μm or more and 1 μm or less. Also, various additives such as antioxidants, heat stabilizers, ultraviolet absorbers, infrared absorbers, pigments, dyes, organic or inorganic particles, antistatic agents, nucleating agents, etc. may be added to the easy-adhesion layer. Good. The resin preferably used for the easy-adhesion layer is preferably at least one resin selected from the group consisting of an acrylic resin, a polyester resin, and a urethane resin from the viewpoint of adhesiveness and handleability. Furthermore, off-annealing under conditions of 140 to 200 ° C. is also preferably used. Here, off-annealing refers to a method in which a polyester film once wound is subjected to heat treatment again.

  The laminated polyester film of the present invention has a laminated structure having a polyester A layer and a polyester B layer having a melting point lower than that of the polyester A layer, and the retardation (Re) with respect to the center and the direction perpendicular to the film surface at a width of 400 mm is both. Since it is 1000 nm or less, it does not exhibit an interference color when mounted on a display device such as a large-screen liquid crystal display. Therefore, a PVA sheet (polarizer) prepared by containing iodine in PVA and orienting it. Are preferably used as polarizing plates.

  In the laminated polyester film of the present invention, when a surface layer is laminated on the outermost surface in order to provide functions such as hard coat property, self-repairing property, antiglare property, antireflection property, low reflection property, or antistatic property. It is preferable to use a production method in which the above-described coating composition is formed by coating, drying and curing.

  The method for producing the surface layer by coating is not particularly limited, but the coating composition is supported by a dip coating method, a roller coating method, a wire bar coating method, a gravure coating method or a die coating method (US Pat. No. 2,681,294). It is preferable to form the surface layer by applying to the material. Further, among these coating methods, the gravure coating method or the die coating method is more preferable as the coating method. Here, the supporting substrate refers to the laminated polyester of the present invention.

  Next, in order to completely remove the solvent by drying the applied liquid film, it is preferable that the liquid film is heated in the drying step. Examples of the drying method include heat transfer drying (adherence to a high-temperature object), convection heat transfer (hot air), radiant heat transfer (infrared ray), and others (microwave, induction heating). Among these, a method using convective heat transfer or radiant heat transfer is preferable because it is necessary to make the drying speed uniform even in the width direction.

  Furthermore, you may perform the further hardening operation (hardening process) by irradiating a heat | fever or an energy ray. In the curing step, the temperature for curing with heat is preferably from room temperature to 200 ° C., and more preferably from 100 ° C. to 200 ° C., more preferably from 130 ° C. to 200 ° C. from the viewpoint of the activation energy of the curing reaction. More preferably, it is not higher than ° C.

Moreover, when hardening with an active energy ray, it is preferable that it is an electron beam (EB ray) and / or an ultraviolet-ray (UV ray) from a versatility point. In the case of curing with ultraviolet rays, the oxygen concentration is preferably as low as possible because oxygen inhibition can be prevented, and curing in a nitrogen atmosphere (nitrogen purge) is more preferable. When the oxygen concentration is high, the hardening of the outermost surface is inhibited, and the surface hardening may be insufficient. Examples of the ultraviolet lamp used when irradiating ultraviolet rays include a discharge lamp method, a flash method, a laser method, and an electrodeless lamp method. Case of UV cured using a high pressure mercury lamp is a discharge lamp type, illuminance of ultraviolet rays 100~3,000mW / cm ^2, preferably 200~2,000mW / cm ^2, more preferably 300~1,500mW / cm ² conditions it is preferable to perform the UV irradiation, the integrated light quantity of ultraviolet 100~3,000mJ / cm ^2, which is a preferably 200~2,000mJ / cm ^2, more preferably 300~1,500mJ / cm ² under the condition that the More preferably, UV irradiation is performed.

  Here, the illuminance of ultraviolet rays refers to the irradiation intensity received per unit area, and varies depending on the lamp output, the emission spectrum efficiency, the diameter of the light emitting bulb, the design of the reflector, and the light source distance to the irradiated object. However, the illuminance does not change depending on the conveyance speed. Further, the UV integrated light amount is irradiation energy received per unit area, and is the total amount of photons reaching the surface. The integrated light quantity is inversely proportional to the irradiation speed passing under the light source, and is proportional to the number of irradiations and the number of lamps.

(Characteristic measurement method and effect evaluation method)
The characteristic measuring method and the effect evaluating method in the present invention are as follows.

(1) Composition of polyester A polyester resin and a film are dissolved in hexafluoroisopropanol (HFIP), and the content of each monomer residue component and by-product diethylene glycol can be quantified using ¹ H-NMR and ¹³ C-NMR. it can. In the case of a laminated film, the components constituting each layer can be collected and evaluated by scraping off each layer of the film according to the laminated thickness. In the following examples and comparative examples, the composition was calculated from the mixing ratio at the time of film production.

(2) Intrinsic viscosity of polyester The intrinsic viscosity of a polyester resin and a film is measured at 25 ° C. using an Ostwald viscometer after dissolving the polyester in orthochlorophenol. In the case of a laminated film, the intrinsic viscosity of each layer can be evaluated by scraping each layer of the film according to the laminated thickness.

(3) Film thickness and layer thickness A film is embedded in an epoxy resin, and a film cross section is cut out with a microtome. The cross section is observed with a transmission electron microscope (TEM H7100 manufactured by Hitachi, Ltd.) at an appropriate magnification to determine the film thickness and the thickness of the polyester layer (in the following Examples and Comparative Examples, the film was observed at a magnification of 5000). .

(4) Using a melting point differential scanning calorimeter (Seiko Denshi Kogyo Co., Ltd., RDC220), measurement and analysis are performed in accordance with JIS K7121-1987 and JIS K7122-1987. Using 5 mg of a polyester film as a sample, the temperature at the top of the endothermic peak obtained from the DSC curve when the temperature is raised from 25 ° C. to 300 ° C. at 20 ° C./min is defined as the melting point. In the case of a laminated film, the melting point of each layer alone can be measured by scraping each layer of the film according to the laminated thickness. In the present invention, in the case of a laminated polyester film having a polyester A layer and a polyester B layer, the melting point of each layer is measured, and the layer having the higher melting point is the polyester A layer and the lower layer is the polyester B layer.

(5) Retardation / Orientation Angle Measurement is performed using a phase difference measuring device (KOBRA-21ADH) manufactured by Oji Scientific Instruments.

(5-1) Retardation in the direction perpendicular to the film surface (Re)
The film is installed in the apparatus so that the film width direction is at an angle of 0 ° defined by the present measuring apparatus, and the retardation at a wavelength of 590 nm and the orientation angle at an incident angle of 0 ° (direction perpendicular to the film surface) are measured.

(5-2) Retardation for an angle inclined by 50 ° with respect to the film surface (R50 °)
A film sample is installed in the same manner as in (5-1), and the retardation (R50 °) at a wavelength of 590 nm and the orientation angle at an incident angle of 50 ° are measured. In addition, the measurement samples in the following examples and comparative examples were collected and used as follows.
-Center in the film width direction: Cut out at 3.5 cm x 3.5 cm square from the center in the film width direction.
-400 mm width: Cut out in a 35 mm × 35 mm square from a 165 mm width position in each of two directions along the width direction from the center in the film width direction. In addition, each measurement of the sample was performed and the average value was made into the value of 400 mm width.
-1000 mm width: Cut out in a 35 mm × 35 mm square from a 465 mm width position in each of two directions along the width direction from the center in the film width direction. In addition, each measurement of the sample was performed and the average value was made into the value of 1000 mm width.
-1500 mm width: Cut out in a 35 mm × 35 mm square from a 715 mm width position in each of two directions along the width direction from the center in the film width direction. In addition, each measurement of the sample was performed and the average value was made into the value of 1500 mm width.
Further, the center in the film width direction (Re · C) and the retardation (Re · E) at a width of 400 mm were applied to the following formula.
Re · E / Re · C.

(6) Storage elastic modulus A film was cut into a rectangular shape having a length of 60 mm and a width of 5 mm in an arbitrary X-direction length and Y-direction, and used as a sample. The storage elastic modulus (E ′) at 70 ° C. was determined under the following conditions using a dynamic viscoelasticity measuring device (DMS6100, manufactured by Seiko Instruments Inc.).
Frequency: 10 Hz, test length: 20 mm, minimum load: about 100 mN, amplitude: 10 μm,
Measurement temperature range: 30 ° C. to 150 ° C., temperature increase rate: 5 ° C./min.

(7) Humidity and heat resistance test A film sample of 5 cm × 5 cm square is placed in a constant temperature / humidity bath with a temperature of 60 ° C. and a humidity of 95%, and is kept for 400 hours. Based on the year), a haze meter (HGM-2GP manufactured by Suga Test Instruments Co., Ltd.) is used for measurement. The measurement is performed at three arbitrary locations, and the average value is adopted.

(8) Refractive index, plane orientation coefficient Sodium D-line (wavelength 589 nm) as a light source, using an Abbe refractometer, the refractive index (nX) in any one direction X in the film plane and the direction orthogonal to the direction X The refractive index (nY) of Y and the refractive index (nZ) in the thickness direction Z are measured. Further, the obtained refractive index is applied to the following formula to calculate the plane orientation coefficient (fn).
fn = (nX + nY) / 2−nZ.
In addition, since the laminated film of the present invention has a polyester A layer and a polyester B layer having a melting point lower than that of the polyester A layer, a plurality of refractive indexes are observed in the X direction, the Y direction, and the Z direction. For this reason, among the observed refractive indexes, in the X direction and the Y direction, the lowest value is the refractive index of the polyester B layer, the highest value is the refractive index of the polyester A layer, and the lowest value is in the Z direction. The value is the refractive index of the polyester A layer, and the highest value is the refractive index of the polyester B layer.

(9) The 85 ° C. heat shrinkage film is cut into a rectangular shape having a length of 150 mm and a width of 10 mm in an arbitrary one direction X and a direction Y orthogonal to the X direction, and used as a sample. Draw marked lines on the sample at intervals of 100 mm, suspend a 3 g weight and place in a hot air oven heated to 85 ° C. for 30 minutes to perform heat treatment. The distance between marked lines after heat treatment is measured, and the heat shrinkage rate is calculated from the change in the distance between marked lines before and after heating by the following formula. For each film, five samples are measured in the X direction and the Y direction for each film, and the average value is evaluated.
Thermal shrinkage (%) = {(distance between marked lines before heat treatment) − (distance between marked lines after heat treatment)} / (distance between marked lines before heat treatment) × 100.

(10) Visibility test One side of a polarizer having a degree of polarization of 99.9% prepared by adsorbing and orienting iodine in PVA is 200 mm from the center in the width direction of the film to 200 mm (film width of 400 mm). ), A sample cut out with a size of 310 mm in the longitudinal direction is passed through a laminator roll set at 85 ° C. to obtain a test piece. The created test piece and the polarizing plate on which no film is attached are superposed in a crossed Nicol arrangement, and the visibility when placed on an LED light source (A3-101 made by Tritech) is confirmed.

  A: Interference color is hardly seen.

  B: Although some interference colors are seen, there is no problem in practical use.

  C: Since interference color is clearly seen, it is not suitable for display applications.

(11) Curling property The test piece obtained in (10) is placed on a horizontal glass plate, the amount of lifting at the four corners in the vertical direction from the glass plate surface is measured, and the amount of lifting (height) of the four corners is measured. The maximum height (maximum value) is evaluated as the curl height of the test piece according to the following criteria.

  A: The curl height is less than 5 mm.

  B: The curl height is 5 mm or more and less than 7 mm.

  C: The curl height is 7 mm or more and less than 10 mm.

  D: The curl height is 10 mm or more.

(12) The test piece obtained in the handleability (10) is observed, and the degree of wrinkle generation due to air entrapment between the polarizer and the film is evaluated according to the following criteria.

  A: No wrinkles are generated.

  B: Some wrinkles are seen at the end, but there is no problem in practical use.

  C: Conspicuous wrinkles were generated.

(13) Heat resistance In the same manner as in (10), one side of a polarizer having a polarization degree of 99.9% created by adsorbing and orienting iodine in PVA is applied in two directions in the width direction from the center portion in the width direction of the film. Each sample is bonded to a sample cut at a size of 95 mm in a longitudinal direction by passing through a laminator roll set at 95 ° C. to give a test piece. The obtained test piece is observed, and the degree of wrinkling due to air entrapment between the polarizer and the film is evaluated according to the following criteria.

  A: No wrinkles are generated.

  B: Some wrinkles are seen at the end, but there is no problem in practical use.

  C: Conspicuous wrinkles were generated.

  In addition, the lamination conditions in this test are severe conditions, and even C evaluation may be sufficiently usable depending on the application.

(14) The test piece obtained in the pencil hardness test (10) is evaluated by scratch hardness (pencil method) described in JIS K5600-5-4 (1999), and HB or higher is regarded as acceptable.

(15) The test piece obtained in the steel wool scratch resistance test (10) is subjected to a rubbing test under the following conditions using a rubbing tester to obtain an index of scratch resistance.
Evaluation environmental conditions: 25 ° C., 60% RH
Rubbing material: Steel wool (manufactured by Nippon Steel Wool Co., Ltd., Grade No. 0000)
Wrap around the tip (1cm x 1cm) of the scraper of the tester that comes into contact with the sample, and fix the band.
Travel distance (one way): 13cm
Rubbing speed: 13 cm / second,
Load: 200 g / cm ² ,
Tip contact area: 1 cm x 1 cm, rubbing frequency: 10 reciprocations.
An oil-based black ink was applied to the back side of the rubbed sample, and scratches on the rubbed portion were visually observed with reflected light, and evaluated according to the following criteria. The above test was repeated three times, and each was evaluated in the following five stages, and the scores were averaged. Three or more points are accepted.
5 points: 0 4 points: 1 or more Less than 5 3 points: 5 or more Less than 10 2 points: 10 or more Less than 20 1 point: 20 or more.

(Manufacture of polyester)
The polyester resin used for film formation was prepared as follows.

(Polyester A)
100 mol% of terephthalic acid (TPA) component (TPA-derived structural unit) as dicarboxylic acid component (structural unit derived from dicarboxylic acid), ethylene glycol (EG) component as glycol-derived structural unit component (glycol-derived structural unit) Polyethylene terephthalate resin (inherent viscosity 0.65) whose (EG-derived structural unit) is 100 mol%.

(Polyester B)
The structural unit derived from terephthalic acid (TPA) is 100 mol% as the structural unit derived from dicarboxylic acid, the structural unit derived from ethylene glycol (EG) is 80 mol% as the structural unit derived from glycol, 1,4-cyclohexanedimethanol ( A copolymer polyester (CHDM) component (CHDM-derived structural unit) is 20 mol% is a resin (inherent viscosity 0.75).

(Polyester C)
Isophthalic acid copolymer in which terephthalic acid component is 82.5 mol% as dicarboxylic acid component, isophthalic acid (IPA) component (IPA-derived structural unit) is 17.5 mol%, and ethylene glycol component is 100 mol% as glycol component Polyethylene terephthalate resin (intrinsic viscosity 0.7).

(Polyester D)
85 mol% terephthalic acid component as dicarboxylic acid component, 15 mol% cyclohexanedicarboxylic acid (CHDC) (CHDC-derived structural unit), 88 mol% ethylene glycol component as glycol component, spiroglycol (SPG) component (derived from SPG) The structural unit is a cyclohexanedicarboxylic acid / spiroglycol copolymerized polyethylene terephthalate resin (inherent viscosity 0.7).

(Polyester E)
Isophthalic acid copolymerized polyethylene terephthalate resin (inherent viscosity of 0) having 82.5 mol% of terephthalic acid component as dicarboxylic acid component, 17.5 mol% of isophthalic acid (IPA) component, and 100 mol% of ethylene glycol component as glycol component .68). (Particle Master)
Polyethylene terephthalate particle master (intrinsic viscosity 0.65) containing polyester A with aggregated silica particles having a number average particle size of 2.2 μm at a particle concentration of 2 mass%.

(Coating composition for forming hard coat layer)
The following materials were mixed and diluted with methyl ethyl ketone to obtain a coating composition for forming a hard coat layer having a solid concentration of 40% by mass.
30 parts by mass of toluene 25 parts by mass of polyfunctional urethane acrylate (KRM 8655 manufactured by Daicel Ornex Co., Ltd.)
25 parts by mass of pentaerythritol triacrylate mixture (Nippon Kayaku Co., Ltd. PET30)
1 part by mass of polyfunctional silicone acrylate (EBECRYL1360, manufactured by Daicel Ornex Co., Ltd.)
3 parts by mass of a photopolymerization initiator (Irgacure 184 manufactured by Ciba Specialty Chemicals).

(Anti-glare layer forming coating composition)
The following materials were mixed and diluted with methyl ethyl ketone to obtain a coating composition for forming an antiglare layer having a solid content of 40% by mass.
30 parts by mass of toluene 50 parts by mass of pentaerythritol triacrylate (Nippon Kayaku Co., Ltd. PET30)
Silica dispersion (number average particle size 1 μm) 12 parts by mass Multifunctional silicone acrylate 1 part by mass (Dycel Ornex Co., Ltd. EBECRYL 1360)
3 parts by mass of a photopolymerization initiator (Irgacure 184 manufactured by Ciba Specialty Chemicals).

(Embodiment 1) Hereinafter, Embodiments 1, 4, and 15 will be read as Reference Examples 1 to 3.
With the composition as shown in the table, the raw materials were fed to separate bent co-directional twin-screw extruders each having an oxygen concentration of 0.2% by volume. That is, the raw material (resin) for forming the polyester A layer was charged into the A layer extruder, and the raw material (resin) for forming the polyester B layer was charged into the B layer extruder. In addition, the vent same direction twin-screw extruder was used for A layer extruder and B layer extruder. Melt A layer extruder cylinder temperature at 280 ° C, B layer extruder cylinder temperature at 270 ° C, short tube temperature after merging with A layer and B layer is 275 ° C, die temperature is 280 ° C, 25 ° C from T-die The sheet was discharged on a cooling drum controlled in temperature. At that time, a wire electrode having a diameter of 0.1 mm was applied electrostatically and adhered to the cooling drum to obtain an unstretched sheet. Next, preheating was performed for 1.5 seconds at a preheating temperature of 85 ° C. in the longitudinal direction, the film was stretched 3.3 times in the longitudinal direction at a stretching temperature of 115 ° C., and immediately cooled with a metal roll whose temperature was controlled at 40 ° C. Next, pre-heating is performed for 1.5 seconds at a preheating temperature of 85 ° C. with a tenter-type horizontal stretching machine, and the film is stretched 3.3 times in the width direction at a stretching first half temperature of 115 ° C., a stretching middle temperature of 135 ° C., and a stretching second half temperature of 145 ° C. In a tenter, heat treatment is performed at a heat treatment temperature of 220 ° C. while relaxing 5% in the width direction, that is, while relaxing in the width direction, a biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm is obtained. It was.

(Example 2)
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained in the same manner as in Example 1 except that the heat treatment temperature was changed to 230 ° C.

Example 3
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained in the same manner as in Example 2 except that the composition was changed as shown in the table.

Example 4
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained in the same manner as in Example 3 except that the longitudinal direction preheating temperature was changed to 70 ° C., the width direction preheating temperature was changed to 70 ° C., and the heat treatment temperature was changed to 220 ° C. .

(Example 5)
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained in the same manner as in Example 2 except that the composition was changed as shown in the table.

(Example 6)
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained in the same manner as in Example 2 except that the composition was changed as shown in the table.

(Example 7)
A biaxially oriented polyester film having a film thickness of 25 μm and a film width of 1550 mm was obtained in the same manner as in Example 2 except that the film thickness was changed.

(Example 8)
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1350 mm was obtained in the same manner as in Example 2 except that the film width was changed.

Example 9
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 500 mm was obtained in the same manner as in Example 2 except that the film width was changed.

(Example 10)
The composition is as shown in the table, and the raw materials are supplied to separate bent co-directional twin-screw extruders each having an oxygen concentration of 0.2% by volume, the A-layer extruder cylinder temperature is 280 ° C., and the B-layer extruder cylinder temperature is Melting at 270 ° C, joining layer A and layer B in a laminating device with 5 slits, the temperature of the short tube after joining is 275 ° C, the base temperature is 280 ° C, and the temperature is controlled to 25 ° C from the T-die. The sheet was discharged on a cooled drum. At that time, a wire electrode having a diameter of 0.1 mm was applied electrostatically and adhered to the cooling drum to obtain an unstretched sheet. Next, preheating was performed for 1.5 seconds at a preheating temperature of 85 ° C. in the longitudinal direction, and the film was stretched 3.3 times in the longitudinal direction at a stretching temperature of 115 ° C. and immediately cooled with a metal roll whose temperature was controlled at 40 ° C. Next, pre-heating is performed for 1.5 seconds at a preheating temperature of 85 ° C. with a tenter-type horizontal stretching machine, and the film is stretched 3.3 times in the width direction at a stretching first half temperature of 115 ° C., a stretching middle temperature of 135 ° C., and a stretching second half temperature of 145 ° C. In the tenter, heat treatment is performed at a heat treatment temperature of 230 ° C. while relaxing 5% in the width direction, that is, relaxing in the width direction, to obtain a biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm. It was.

(Example 11)
The composition is as shown in the table, and the raw materials were supplied to separate bent co-directional twin-screw extruders each having an oxygen concentration of 0.2% by volume, the A-layer extruder cylinder temperature was 280 ° C., and the B-layer extruder cylinder temperature was 270 After melting at 0 ° C., the A layer and the B layer were joined by a laminating apparatus having 9 slits, and the short tube temperature after joining was 275 ° C., the die temperature was 280 ° C., and the temperature was controlled to 25 ° C. from the T die. The sheet was discharged on a cooling drum. At that time, a wire electrode having a diameter of 0.1 mm was applied electrostatically and adhered to the cooling drum to obtain an unstretched sheet. Next, preheating was performed for 1.5 seconds at a preheating temperature of 85 ° C. in the longitudinal direction, the film was stretched 3.3 times in the longitudinal direction at a stretching temperature of 115 ° C., and immediately cooled with a metal roll whose temperature was controlled at 40 ° C. Next, pre-heating is performed for 1.5 seconds at a preheating temperature of 85 ° C. with a tenter-type horizontal stretching machine, and the film is stretched 3.3 times in the width direction at a stretching first half temperature of 115 ° C., stretching middle temperature of 135 ° C. In the tenter, heat treatment is performed at a heat treatment temperature of 230 ° C. while relaxing 5% in the width direction, that is, relaxing in the width direction, to obtain a biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm. It was.

(Example 12)
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained in the same manner as in Example 10 except that the composition was changed as shown in the table.

(Example 13)
A biaxially oriented polyester film having a film thickness of 32 μm and a film width of 1350 mm was obtained in the same manner as in Example 8 except that the heat treatment temperature was changed to 240 ° C.

(Example 14)
A biaxially oriented polyester film having a film thickness of 32 μm and a film width of 1550 mm was obtained in the same manner as in Example 8 except that the composition was changed as shown in the table.

(Example 15)
Example except that the composition was changed as shown in the table, and the stretching temperature in the longitudinal direction was 95 ° C, the first half temperature in the width direction was 95 ° C, the middle stretching temperature was 95 ° C, the second half stretching temperature was 95 ° C, and the heat treatment temperature was 235 ° C. In the same manner as in Example 2, a biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained.

(Comparative Example 1)
The composition was changed as shown in the table, except that the stretching temperature in the longitudinal direction was 95 ° C, the first half temperature in the width direction was 95 ° C, the middle stretching temperature was 95 ° C, and the second half stretching temperature was 95 ° C. A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained.

(Comparative Example 2)
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 1550 mm was obtained in the same manner as in Comparative Example 1 except that the draw ratio in the longitudinal direction was 3 times and the draw ratio in the width direction was 3.8 times.

(Comparative Example 3)
A biaxially oriented polyester film having a film thickness of 40 μm and a film width of 200 mm was obtained in the same manner as in Example 1 except that the film width was changed.

(Examples 2-2, 7-2, 8-2, 11-2)
Slot die coater by controlling the flow rate of the coating composition for forming a hard coat layer on the biaxially oriented polyester films of Examples 2, 7, 8, and 11 described above so that the thickness after drying becomes 5 μm. And dried at 100 ° C. for 1 minute to remove the solvent. Next, the film coated with the hard coat layer was irradiated with 300 mJ / cm ² ultraviolet rays using a high-pressure mercury lamp to obtain a laminated polyester film on which the hard coat layer was laminated.

(Examples 2-3, 7-3, 8-3, 11-3)
On the biaxially oriented polyester films of Examples 2, 7, 8 and 11, the antiglare layer-forming coating composition is applied with a slot die coater and dried at 100 ° C. for 1 minute to remove the solvent. did. Next, the film coated with the antiglare layer was irradiated with 300 mJ / cm ² of ultraviolet rays using a high-pressure mercury lamp to obtain a laminated polyester film in which the antiglare layer having a thickness of 5 μm was laminated.

  The unit in the “resin” column of the table is mass%.

  The laminated polyester film of the present invention has a laminated structure having a polyester A layer and a polyester B layer having a melting point lower than that of the polyester A layer. Therefore, when mounted on a display device such as a large-screen liquid crystal display, it does not exhibit an interference color. Used as a plate.

A Laminated film B Laminated film width direction C Laminated film width direction center (Laminated film width direction center line)

Claims (15)

A laminated polyester film of 10 layers or less having a polyester A layer and a polyester B layer having a melting point lower than that of the polyester A layer, the retardation (Re) with respect to the center of the laminated film in the width direction and the direction perpendicular to the film surface at 400 mm width. both Ri der below 500 nm, the laminated polyester film retardation for 50 ° oblique angle to the film plane (R50 °) is Ru der than 1000nm or less 1 nm. Here, the melting points of the polyester A layer and the polyester B layer were measured in accordance with JIS K7121-1987 and K7122-1987, and from the DSC curve when the temperature was raised from 25 ° C. to 300 ° C. at 20 ° C./min. The temperature at the top of the obtained endothermic peak is taken as a value, and when a plurality of endothermic peaks appear, the temperature at which the absolute value of the heat flow is the largest is taken. The laminated polyester film according to claim 1, wherein the retardation (Re · C) at the center in the width direction of the laminated film and the retardation (Re · E) at a width of 400 mm satisfy the following formula (I).
Re · E / Re · C ≦ 1.5 (I) The laminated polyester film according to claim 1 or 2, wherein a film haze difference (Δhaze) before and after holding the film for 400 hours under a condition of a temperature of 60 ° C and a humidity of 95% is less than 1%. A retardation (R50 °) with respect to an angle inclined by 50 ° with respect to the film surface at the center in the width direction of the laminated film is 1 nm or more and 1000 nm or less, and an arbitrary one direction in the film surface is a direction X and a direction orthogonal to the direction X Is a direction Y, the storage elastic modulus in the film direction X and the direction Y at 95 ° C is 800 MPa or more, respectively. Assuming that one arbitrary direction in the film plane is the direction X, the direction perpendicular to the direction X is the direction Y, and the film thickness direction is the direction Z, the average value of the refractive indexes in the X, Y, and Z directions of the polyester B layer is 1. It is 51 or more and 1.57 or less, The laminated polyester film in any one of Claims 1-4. The laminated polyester film according to claim 5, wherein the heat shrinkage rate at 85 ° C in the direction X is 0.5% or less. The laminated polyester film according to claim 5 or 6, wherein the thermal shrinkage rate at 85 ° C in the direction Y is 0.5% or less. The laminated polyester film according to any one of claims 1 to 7, wherein the polyester A layer is located in at least one outermost layer, and the plane orientation coefficient of the A layer is greater than 0.11 and less than 0.16. The laminated polyester film according to claim 1, which has a three-layer configuration of A layer / B layer / A layer. The laminated polyester film according to any one of claims 1 to 9, wherein the thickness per layer of the A layer is less than 3.2 µm. The polyester B layer contains from 60 mol% to 90 mol% of structural units derived from ethylene glycol and from more than 10 mol% to 40 mol% or less of structural units derived from other diols with respect to the structural units derived from diol. The laminated polyester film according to any one of claims 1 to 10. The polyester B layer has a structural unit derived from terephthalic acid of 60 mol% or more and 90 mol% or less and a structural unit derived from other dicarboxylic acid of more than 10 mol% and 40 mol% relative to the structural unit derived from dicarboxylic acid. The laminated polyester film according to any one of claims 1 to 11, which is contained below. Orthogonal in the center in the lateral direction of the laminated film, the retardation for 50 ° oblique angle to the film plane (R50 °) is not less 1nm or more 1 0 nm or less, any one direction in the film plane direction X, the direction X When the direction to perform is direction Y and the film thickness direction is direction Z, the average value of the refractive index in the X, Y and Z directions of the polyester B layer is 1.51 or more and 1.57 or less, and A layer / B layer / A The laminated polyester film according to claim 1, which has a three-layer structure.
One or more functions selected from the group consisting of hard coat properties, self-repair properties, antiglare properties, antireflection properties, low reflectivity properties, and antistatic properties are exhibited on at least one outermost surface of the laminated polyester film. The layer is laminated | stacked, The laminated polyester film in any one of Claims 1-13 characterized by the above-mentioned.
The polarizing plate which has a polarizer protective film on both surfaces of a polarizer, Comprising: The polarizer protective film used for at least one surface is the polarizing plate which is a laminated polyester film in any one of Claims 1-14 .

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