JP2015145077A - Polyester film for release film - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a biaxially oriented polyester film suitable for optical use, which shows sufficient winding property, antistatic property and slipping property when used, for example, for a substrate of a release film for manufacturing a polarizing plate, and even when a release layer is applied in a fast process, and which enables production of a high-quality release film for manufacturing a polarizing plate.SOLUTION: A polyester film for a release film is provided; and the film consists of a polyester film having a multilayer structure of at least three layers, in which both outer layers contain at least two types of particles having different particle sizes. A value (St/Sa) obtained by dividing maximum cross-sectional roughness (St) of both surfaces of the film by average roughness (Sa) is in a range from 65 to 90.

Description

  The present invention relates to a polyester film for a release film, and particularly to a biaxially oriented polyester film that is suitably used for a release film for a polarizing plate for liquid crystal display applications and the like.

  Polyester films represented by polyethylene terephthalate and polyethylene naphthalate have excellent mechanical strength, dimensional stability, flatness, heat resistance, chemical resistance, optical properties, etc. It is used in applications. As one of the uses, it may be used as a release polyester film for a polarizing plate of a liquid crystal display (LCD).

  In recent years, with the rapid spread of mobile phones and personal computers, the demand for liquid crystal displays that are thinner, lighter, consume less power, and have higher image quality than the conventional display CRT is growing significantly. The technology has also grown significantly with the increase in screen size.

  As an example of increasing the screen size of LCD, recently, LCD is used for large TV applications of 30 inches or more. With such an increase in demand for LCD itself and an increase in LCD screen, the use area of the polarizing plate, which is a member of the LCD, will also increase, and the release polyester film for polarizing plate will also increase the productivity and supply amount There is a need to increase the cost and reduce the cost.

  When the processing line speed is increased to increase the productivity of the polarizing plate release film, applying a polyester film with a conventional design presents technical issues in terms of film slipperiness, winding characteristics, and charging properties. I know that there is. Due to these problems, the productivity of the release film cannot be increased, and when trying to increase the productivity by applying the polyester film of the conventional design, the yield is reduced, and as a result Rather, problems that reduce productivity occur.

JP 2009-12254 A

  The present invention has been made in view of such problems, and the problem to be solved is, for example, when a release layer is coated at a high speed when used as a substrate for a release film for producing a polarizing plate. However, an object of the present invention is to provide a biaxially oriented polyester film suitable for optical use, which has sufficient winding properties, charging properties, and slip properties and can produce a high-quality release film for producing a polarizing plate.

  As a result of intensive studies to solve the above problems, the present inventors have found that the above problems can be easily solved by blending specific particles and having a specific structure, and complete the present invention. It came to.

  That is, the gist of the present invention is a polyester film having a laminated structure of at least three layers containing at least two kinds of particles having different particle diameters in both outer layers, and the maximum cross-sectional roughness (St) on both surfaces of the film. Is a polyester film for releasing a polarizing plate, wherein a value (St / Sa) obtained by dividing the value by the average roughness (Sa) is in the range of 65 to 90.

  According to the present invention, when used as a base material for a release film for producing a polarizing plate, the winding properties, charging properties, and slip properties are sufficient even if the release processing is performed at a high speed, thereby producing a high-quality polarizing plate. The biaxially oriented polyester film for optical applications capable of producing a mold release film can be provided, and the industrial value of the present invention is high.

  The polyester referred to in the present invention refers to a polymer containing an ester group obtained by polycondensation from a dicarboxylic acid and a diol or from a hydroxycarboxylic acid. Examples of the dicarboxylic acid include terephthalic acid, succinic acid, isophthalic acid, adipic acid, azelaic acid, sebacic acid, dodecanedioic acid, 2,6-naphthalenedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, and the diol includes ethylene. Glycol, 1,3-propanediol, 1,6-hexanediol, 1,4-butanediol, diethylene glycol, triethylene glycol, neopentyl glycol, 1,4-cyclohexanedimethanol, polyethylene glycol, etc. as hydroxycarboxylic acids Can be exemplified by p-hydroxybenzoic acid, 6-hydroxy-2-naphthoic acid and the like.

  Typical examples of such polymers include polyethylene terephthalate, polybutylene terephthalate, and polyethylene-2,6-naphthalate. These polymers may be homopolymers or may be a copolymer of the third component. As the film of the present invention, a biaxially stretched film is preferably used from the viewpoint of excellent strength and dimensional stability.

  Crosslinked polymer particles may be mentioned as one of suitable particles added as small particles to both outer layers of the polyester film in the present invention. The average particle diameter is usually 0.2 to 1.0 μm, preferably 0.3 to 0.7 μm. When the average particle size is less than 0.2 μm, the average roughness (Sa) when a polyester film is used cannot be reached to a sufficiently high value, and a film within the scope of the present invention cannot be designed. There is. Conversely, if it exceeds 1.0 μm, the average roughness (Sa) in the case of a polyester film cannot be made sufficiently low, and the maximum cross-sectional roughness (St) is related to the average roughness (Sa). May be difficult to control within the scope of the present invention.

  The preferable content of these small particles is usually 0.05 to 0.5% by weight with respect to the outer layer containing the particles. When the content of the cross-linking agent polymer particles A is less than 0.05% by weight, the formation of surface protrusions is not sufficient, so that the slipperiness is lowered and scratches are easily generated. The film quality may be deteriorated due to the occurrence of foreign matter or the like. On the other hand, when the content of the small particles is more than 0.5% by weight, the transparency of the film becomes low due to surface roughening, and the visual inspection tends to be inferior.

  Crosslinked polymer particles can usually be obtained as follows. That is, a compound (A) having only one aliphatic unsaturated bond in a molecule is copolymerized with a compound (B) having two or more aliphatic unsaturated bonds in the molecule as a crosslinking agent. It is obtained. Examples of the compound (A) which is a component of the copolymer include acrylic acid, crotonic acid, methacrylic acid, and lower alkyl esters such as methyl ester and ethyl ester, or glycidyl ester, maleic anhydride and alkyl thereof. Derivatives, vinyl glycidyl ether, vinyl acetate, acrylonitrile, styrene and substituted products thereof. Examples of the compound (B) include divinylbenzene, ethylene glycol dimethacrylate, butylene glycol acrylate and the like.

  Typical examples of these copolymers include copolymers of methacrylic acid and divinylbenzene, styrene and divinylbenzene, and methacrylic acid and ethylene glycol dimethacrylate. In the present invention, the compound (A ) And (B) may be used to obtain crosslinked polymer particles.

  The crosslinked polymer particles that can be used in the present invention preferably have a particle size distribution (r) of 2.0 to 5.0 and an average particle size (d) of 0.2 to 1.0 μm. In order to obtain particles having (r) and an average particle diameter (d), those obtained directly by suspension polymerization or emulsion polymerization may be blended. It is preferable to obtain by pulverizing and classifying a crosslinked polymer having a size of several tens μm to several hundreds μm.

  One of suitable particles added as large particles to both outer layers of the polyester film of the present invention is inert particles. The average particle diameter of the inert particles is preferably 0.4 to 2.0 μm, more preferably 0.5 to 1.5 μm, and still more preferably 0.6 to 1.0 μm. The addition amount of the inert particles is preferably 0.05 to 2.0% by weight, more preferably 0.1 to 1.0% by weight with respect to the outer layer of the film.

  When the average particle diameter of the inert particles is smaller than 0.5 μm, the film surface protrusions due to the particles are not sufficiently developed, and the effect of improving the generation of scratches and winding characteristics may not be recognized. On the other hand, if the average particle size is larger than 2.0 μm, the protrusions appearing on the film surface become large, and it may appear as a bright spot defect.

  When the added amount of the inert particles is less than 0.05% by weight, the number of projections on the film surface due to the particles is not sufficient, and the effect of improving the winding characteristics such as the occurrence of scratches and winding deviation may not be observed. is there. On the other hand, when the addition amount exceeds 1.0% by weight, protrusions appearing on the film surface become large, and it may appear as a bright spot defect.

  The kind of the inert particles that can be particularly preferably used in the present invention is not particularly limited as long as it is a particle capable of imparting slipperiness, and specific examples thereof include, for example, silica, calcium carbonate, magnesium carbonate, Examples of the particles include barium carbonate, calcium sulfate, calcium phosphate, magnesium phosphate, kaolin, aluminum oxide, and titanium oxide. Further, the heat-resistant organic particles described in JP-B-59-5216, JP-A-59-217755 and the like may be used. Examples of other heat-resistant organic particles include thermosetting urea resin, thermosetting phenol resin, thermosetting epoxy resin, benzoguanamine resin, etc., from the viewpoint of transparency and handleability when formed into a film. Silica is preferably used.

  On the other hand, the shape of the particles to be used is not particularly limited, and any of a spherical shape, a block shape, a rod shape, a flat shape, and the like may be used. Moreover, there is no limitation in particular also about the hardness, specific gravity, a color, etc. These series of particles may be used in combination of two or more as required.

  The polyester film of the present invention has an essential condition that the value (St / Sa) obtained by dividing the maximum cross-sectional roughness (St) on both sides of the film by the average roughness (Sa) is in the range of 65 to 90, preferably It is in the range of 70 to 80. If St / Sa is greater than 90, the fine roughness of the film surface is insufficient, and static electricity is generated when the polyester film is unwound, or blocking is caused by the product rolled up with the product after the release layer is applied. There is a concern that it may occur. When St / Sa is smaller than 65, light reflection is generated on the film surface because the film surface is too finely rough, and the inspectability of the product after the release layer is applied is inferior. In addition, due to the fact that sufficiently high protrusions are not sufficiently present on the film surface, winding deviation easily occurs during product winding.

  In the present invention, even if the surface of the particles is treated with various surface treatment agents such as a silane coupling agent or a titanium coupling agent, the effect is sufficiently exhibited.

  Hereinafter, although the manufacturing method of the film of this invention is demonstrated concretely, as long as the structure of this invention is satisfied, this invention is not specifically limited to the following illustrations.

  Polyester chips dried by a known method are supplied to a melt extrusion apparatus and heated to a temperature equal to or higher than the melting point of each polymer to melt. Next, the molten polymer is extruded from a die and rapidly cooled and solidified on a rotary cooling drum so that the temperature is equal to or lower than the glass transition temperature to obtain a substantially amorphous unoriented sheet. In this case, in order to improve the flatness of the sheet, it is preferable to improve the adhesion between the sheet and the rotary cooling drum. In the present invention, an electrostatic application adhesion method and / or a liquid application adhesion method is preferably employed.

  In the present invention, the sheet thus obtained is stretched biaxially to form a film. Specifically describing the stretching conditions, the unstretched sheet is preferably stretched 2 to 6 times at 70 to 145 ° C. in the longitudinal direction to form a longitudinal uniaxially stretched film, and then 2 to 90 to 160 ° C. in the lateral direction. It is preferable to perform ~ 6 times stretching and heat treatment at 150 to 240 ° C for 1 to 600 seconds. Further, at this time, a method of relaxing 0.1 to 20% in the longitudinal direction and / or the transverse direction in the maximum temperature zone of the heat treatment and / or the cooling zone at the heat treatment outlet is preferable. Further, it is possible to add re-longitudinal stretching and re-lateral stretching as necessary.

  If the polyester film of the present invention is within the range not impairing the effects of the present invention, it may be stretched in the longitudinal direction as necessary to improve the required properties such as antistatic properties, weather resistance and surface hardness. After the completion, so-called in-line coating may be performed in which coating is performed before the entrance of the tenter for transverse stretching and drying is performed in the tenter. Various coatings may be performed by offline coating after film production. Such a coat may be either single-sided or double-sided. The coating material may be either water-based and / or solvent-based for offline coating, but is preferably water-based or water-dispersed for in-line coating.

  The polyester film of the present invention can be mixed with other thermoplastic resins such as polyethylene naphthalate and polytrimethylene terephthalate as long as the effects of the present invention are not impaired. Further, an ultraviolet absorber, an antioxidant, a surfactant, a pigment, a fluorescent brightening agent, and the like can be mixed.

  When a release layer is installed on the polyester film of the present invention, the material constituting the release layer is not particularly limited as long as it has releasability, and a type mainly composed of a curable silicone resin may be used. Alternatively, a modified silicone type obtained by graft polymerization with an organic resin such as a urethane resin, an epoxy resin, or an alkyd resin may be used. Among them, when the curable silicone resin is a main component, the release property is good. Types of curable silicone resins include solvent addition type, solvent condensation type, solvent ultraviolet ray curable type, solventless addition type, solventless condensation type, solventless ultraviolet ray curable type, solventless electron beam curable type, etc. Can be used.

  EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to a following example, unless the summary is exceeded. Various physical properties and characteristics are measured or defined as follows.

(1) Average particle size The particle size was measured by a sedimentation method based on Stokes' resistance law using a centrifugal sedimentation type particle size distribution analyzer SA-CP3 manufactured by Shimadzu Corporation.

(2) Arithmetic average roughness (Sa) and maximum cross-sectional roughness (St) measurement of the film surface The measurement surface of the sample film is used as the measurement surface of the sample film, and the direct phase detection interferometry, so-called Michelson interference is used 2 Arithmetic average roughness (Sa) and maximum cross-sectional roughness (St) were measured by a non-contact surface measurement system “Micromap 512” manufactured by Micromap Co., Ltd. using a beam interference method. The measurement wavelength is 530 nm, the objective lens is 20 times, and the 20 ° field of view is measured, and the arithmetic average roughness (Sa) and the maximum cross-sectional roughness (St) are measured at a total of 12 points. A total of 10 average values excluding the maximum and minimum values was adopted.

(3) Winding characteristics (winding deviation)
The winding characteristics were determined according to the following criteria from the generation ratio (number of winding deviations / total number of products) of winding misalignment when a product having a width of 1300 mm and a winding length of 8000 m was collected from a 4000 mm width master roll.
○: 0 to 10%
×: 10% or more

(4) Amount of charge After winding a product with a width of 1300 mm and a winding length of 8000 m by the above-mentioned method, the film is unwound by two rounds on the outer periphery, and the electrostatic property on the inner surface of the film generated at that time is digital electrostatic potential. It was measured with a measuring instrument (KSD-1000, manufactured by Kasuga Denki).

(5) Blocking property 100 parts of curable silicone resin (“KS-779H” manufactured by Shin-Etsu Chemical), 1 part of curing agent (“CAT-PL-8” manufactured by Shin-Etsu Chemical) on a polyester film, mixed with methyl ethyl ketone (MEK) / toluene A release agent composed of 2200 parts of solvent system was applied so that the coating amount was 0.1 g / mm ² and dried at 170 ° C. for 10 seconds to obtain a release film. Ten sets of the obtained release film were prepared so that the release layer coating surface and the plane surface faced, and pressed for 48 hours at 40 ° C. and 80% RH in a hot press machine at 10 kg / cm 2. . One set of film in the middle was taken out after hot pressing, and its blocking property was evaluated according to the following criteria.
○: The paired film is peeled off just by lifting the film on one side. △: When the film on one side is lifted, the paired film is also attached. Can be peeled without ×: When a film on one side is lifted, a pair of films are also attached, and when they are peeled off, a crisp sound is made

(6) Visual inspection property After applying a release layer to the polyester film according to the contents described in (5), the film was visually observed under the reflection of a fluorescent lamp, and the visual inspection property was evaluated according to the following criteria.
<Criteria for visual inspection under reflected light>
(Good inspection) ○ ＞ △ ＞ × (Inspection failure)

Example 1:
(Production of crosslinked polymer fine powder)
A homogeneous solution of 100 parts of methyl methacrylate, 25 parts of divinylbenzene, 22 parts of ethylvinylbenzene, 1 part of benzoyl peroxide and 100 parts of toluene was dispersed in 700 parts of water.
Next, polymerization was performed by heating to 80 ° C. with stirring for 8 hours under a nitrogen atmosphere.
The average particle diameter of the obtained crosslinked polymer granules having ester groups was about 0.1 mm. The granules were washed with demineralized water and extracted three times with 500 parts of toluene to remove a small amount of unreacted monomer and linear polymer. Next, the polymer particles were pulverized with an attritor for 2 hours and further with a sand grinder manufactured by Igarashi Machine Co., Ltd. for 5 hours to obtain a crosslinked polymer fine powder having an average particle size of 0.6 μm. Next, after removing large particles with a super decanter, a crosslinked polymer fine powder having a particle size distribution (r) of 3.1 and an average particle size of 0.5 μm was obtained using a 2400 mesh filter.

(Production method of polyester chip A)
Take 100 parts of dimethyl terephthalate, 70 parts of ethylene glycol, and 0.07 part of calcium acetate monohydrate in a reactor, heat up and evaporate methanol to conduct transesterification, and take about 4 and a half hours after starting the reaction. The temperature was raised to 230 ° C. to substantially complete the transesterification reaction. Next, 0.04 part of phosphoric acid and 0.035 part of antimony trioxide were added and polymerized in accordance with a conventional method. That is, the reaction temperature was gradually raised to finally 280 ° C., while the pressure was gradually reduced to finally 0.05 mmHg. After 4 hours, the reaction was completed, and chips were obtained according to a conventional method to obtain polyester A.

(Production method of polyester chip B)
When manufacturing the said polyester A, 6000 ppm of the crosslinked polymer fine powder obtained by the said method with an average particle diameter of 0.5 micrometer was added, and the polyester B was obtained.

(Production method of polyester chip C)
When manufacturing the said polyester A, 20000 ppm of calcium carbonate with an average particle diameter of 0.8 micrometer was added, and the polyester C was obtained.

(Manufacture of polyester film)
Mixing the above-mentioned polyester A, polyester B, and polyester C in proportions of 65%, 20%, and 15% as the raw material for the A layer, and using the raw material of 100% polyester A as the raw material for the B layer, After each was supplied and melted at 285 ° C., the A layer was the outermost layer (surface layer), the B layer was the intermediate layer, and on the casting drum cooled to 40 ° C., two types and three layers (ABA) were formed. A non-oriented sheet was obtained by co-extrusion and cooling and solidification so that the ratio was A: B: A = 3: 32: 3. Next, the film was stretched 2.8 times in the machine direction at a film temperature of 125 ° C. using the roll peripheral speed difference, then led to a tenter, stretched 4.2 times at 100 ° C. in the transverse direction through a preheating step, and 210 ° C. After heat treatment for 10 seconds, 7% relaxation was applied in the width direction at 180 ° C. to obtain a polyester film having a width of 4000 mm and a thickness of 38 μm.

Example 2:
A polyester film was obtained in the same manner as in Example 1 except that polyester A, polyester B, and polyester C were mixed in proportions of 55%, 30%, and 15%, respectively. The obtained polyester film resulted as shown in Table 1.

Example 3:
A polyester film was obtained in the same manner as in Example 1 except that polyester A, polyester B, and polyester C were mixed in proportions of 45%, 40%, and 15%, respectively. The obtained polyester film resulted as shown in Table 1.

Example 4:
A polyester film was obtained in the same manner as in Example 1 except that polyester A, polyester B, and polyester C were mixed in proportions of 35%, 50%, and 15%, respectively. The obtained polyester film resulted as shown in Table 1.

Example 5:
A polyester film was obtained in the same manner as in Example 1 except that polyester A, polyester B, and polyester C were mixed in proportions of 45%, 30%, and 25%, respectively. The obtained polyester film resulted as shown in Table 1.

Comparative Example 1:
A polyester film was obtained in the same manner as in Example 1 except that polyester A and polyester C were 85% and 15% respectively. The obtained polyester film resulted as shown in Table 1.

Comparative Example 2:
A polyester film was obtained in the same manner as in Example 1 except that polyester A, polyester B, and polyester C were mixed in proportions of 75%, 10%, and 15%, respectively. The obtained polyester film resulted as shown in Table 1.

Comparative Example 3:
A polyester film was obtained in the same manner as in Example 1 except that the raw material composition of the A layer was 15% and 85% respectively for polyester A and polyester B. The obtained polyester film resulted as shown in Table 1.

  The film of the present invention can be suitably used as a base material for a release film for producing a polarizing plate, for example.

Claims (1)

It is a polyester film having a laminated structure of at least three layers, containing at least two kinds of particles having different particle sizes in both outer layers, and the maximum cross-sectional roughness (St) on both surfaces of the film is the average roughness (Sa). The polyester film for a release film, wherein the divided value (St / Sa) is in the range of 65 to 90.