JP5391618B2 - White film and surface light source using the same - Google Patents

Description

  The present invention relates to an improvement of a white film. More specifically, the present invention relates to a white film suitable as a reflecting member (a reflecting plate and a reflector) for a surface light source, which can obtain a surface light source that is brighter and excellent in illumination efficiency.

  In recent years, many displays using liquid crystals have been used as display devices for personal computers, televisions, mobile phones, and the like. Since these liquid crystal displays themselves are not light emitters, they can be displayed by installing a surface light source called a backlight from the back side and irradiating light. Further, the backlight has a structure of a surface light source called a side light type or a direct type in order to meet the requirement that the entire screen should be irradiated uniformly, not just light. In particular, for a thin liquid crystal display used for a notebook personal computer or the like for which a thin and small size is desired, a sidelight type, that is, a backlight of a type that irradiates light from the side of a screen is applied.

  In general, this sidelight type backlight uses a cold cathode ray tube as an illumination light source from the edge of the light guide plate and uses a light guide plate that uniformly propagates and diffuses light to uniformly illuminate the entire liquid crystal display. Is adopted. In this illumination method, in order to use light more efficiently, a reflector is provided around the cold cathode ray tube, and the light guide plate is used to efficiently reflect the light diffused from the light guide plate to the back surface toward the liquid crystal screen. A reflection plate is provided below. Thereby, the loss of light from the cold cathode ray tube is reduced, and the function of brightening the liquid crystal screen is provided.

  On the other hand, for large screens such as liquid crystal televisions, the direct light type has been adopted because it is not possible to increase the brightness of the large screen with the edge light method. In this method, a cold cathode ray tube is provided in parallel at the lower part of the liquid crystal screen, and the cold cathode ray tubes are arranged in parallel on the reflector. The reflecting plate may be a flat plate or a cold cathode ray tube formed into a semicircular concave shape.

  Reflectors and reflectors used in such surface light sources for liquid crystal screens (collectively referred to as surface light source reflecting members) are required to have a high reflection function as well as a thin film. A single film containing fine bubbles inside, or a laminate of these films and a metal plate, a plastic plate or the like has been used. In particular, when a film containing fine bubbles inside is used, it is widely used because of its excellent brightness improvement effect and uniformity (Patent Documents 1 and 2).

By the way, the application of the liquid crystal screen has been widely used in various devices such as a stationary personal computer, a television, and a mobile phone display in recent years in addition to a conventional notebook personal computer. With the demand for higher-definition images on LCD screens, improvements have been made to increase the brightness of LCD screens to make the images clearer and easier to see. Lighting sources (for example, cold cathode ray tubes) Has become higher brightness and higher output.
JP-A-6-322153 JP-A-7-118433

  However, in the case of the above conventional film, since the light reflectivity is insufficient, when used in a reflector or reflector as a surface light source reflecting member, a part of the light of the illumination light source is transmitted to the opposite surface. As a result, there is a problem that the luminance (brightness) of the liquid crystal screen is insufficient, and the illumination efficiency is reduced due to light transmission loss from the illumination light source. For this reason, the white film has been required to further improve the reflectance and concealability.

Therefore, the present invention employs the following means in order to solve such problems. That is, the white film of the present invention comprises (1) a resin (B) incompatible with the crystalline resin (A) in a matrix containing at least the crystalline resin (A) (hereinafter referred to as incompatible resin (B)). In a white film having a layer (S layer) having bubbles inside, the incompatible resin (B) is an amorphous resin (B1), and the incompatible resin (B1). ) Is a glass transition temperature Tg1 of 170 ° C. or higher, the content is 10% by weight or higher based on the total material constituting the S layer, the melting point Tm of the crystalline resin (A) + 20 ° C., and the shear rate 200 sec ^−1. A white film in which the melt viscosity η1 (Pa · s) of the crystalline resin (A) and the melt viscosity η2 (Pa · s) of the incompatible resin (B) satisfy the following (1) and (2):
(1) −0.1 ≦ log ₁₀ (η2 / η1) ≦ 0.45
(2) 0.95 ≦ log ₁₀ (η2) / log ₁₀ (η1) ≦ 1.20 .

  The white film of the present invention is excellent in reflection characteristics, lightness, and the like, particularly when used as a reflector or reflector in a surface light source, can brightly illuminate the liquid crystal screen, making the liquid crystal image clearer and easier to see, It is useful.

  The inventors of the present invention have intensively studied a white film having high reflection characteristics, and have determined that the above problems can be solved at once by controlling the melt viscosity of the resin constituting the film to a specific condition.

That is, the reflective film of the present invention is a resin (B) incompatible with the crystalline resin (A) in a matrix containing at least the crystalline resin (A) (hereinafter referred to as incompatible resin (B)). In the white film having a layer (S layer) having bubbles inside, the melting point Tm of the crystalline resin (A) + 20 ° C., the melt viscosity η1 of the crystalline resin (A) at a shear rate of 200 sec ⁻¹ (Pa The melt viscosity η2 (Pa · s) of s) and the incompatible resin (B) satisfies the following (1) and (2).
(1) −0.1 ≦ log ₁₀ (η2 / η1) ≦ 0.45

(2) 0.95 ≦ log ₁₀ (η2) / log ₁₀ (η1) ≦ 1.20
By adopting such a configuration, it is possible to dramatically improve the whiteness, light reflectivity, concealment and the like of the white film, and as a result, for example, when used as a reflective member of a liquid crystal display, a high brightness improvement effect is obtained. It can be done.

  The white film of the present invention needs to have bubbles inside. In order to obtain this configuration, the matrix containing at least the crystalline resin (A) contains the incompatible resin (B) as a core material, and this is processed into a sheet shape. Alternatively, by stretching biaxially, bubbles can be formed inside by peeling at the interface between the matrix and the core material.

  The white film of the present invention contains at least a crystalline resin (A) in a matrix. In the present invention, the matrix resin (sometimes abbreviated as “matrix”) is a resin contained in the S layer and refers to all resins other than the incompatible resin (B). By including at least the crystalline resin (A) as a matrix, the S layer can be oriented and crystallized by stretching and heat treatment, and a white film excellent in mechanical strength and heat resistance can be obtained. Here, the crystalline resin means that the resin is heated from 25 ° C. to 300 ° C. at a temperature rising rate of 20 ° C./min (1stRUN) according to JIS K7122 (1999), and the state In the differential scanning calorimetry chart of 2ndRUN obtained by rapidly cooling to 25 ° C. or less after holding for 5 minutes and then increasing the temperature from room temperature to 300 ° C. at a temperature increase rate of 20 ° C./min. It is a resin in which an exothermic peak associated with is observed. More specifically, a resin having a crystallization enthalpy ΔHcc of 1 J / g or more determined from the area of the exothermic peak is defined as a crystalline resin. In the white film of the present invention, when there is one kind of crystalline resin among the resins constituting the matrix, the resin is designated as crystalline resin (A). When a plurality of crystalline resins constituting the matrix are included, the crystalline resin that is the main component of the crystalline resins is referred to as crystalline resin (A). In the white film of the present invention, the crystalline resin (A) is preferably a resin having a crystallization enthalpy ΔHcc of 5 J / g or more, more preferably 10 J / g or more, and even more preferably 15 J / g or more. By setting the crystallization enthalpy of the crystalline resin (A) in the above-mentioned range in the white film of the present invention, it becomes possible to further enhance the orientation crystallization by stretching and heat treatment, and as a result, more mechanical strength and heat resistance. The white film can be made excellent.

  The crystalline resin (A) used for the white film of the present invention must satisfy the above-mentioned requirements. Specific examples thereof include polyethylene terephthalate, polyethylene-2, 6-naphthalate, polypropylene terephthalate, and polybutylene terephthalate. Polyester resins such as polylactic acid, polyolefin resins such as polyethylene, polystyrene and polypropylene, polyamide resins, polyimide resins, polyether resins, polyester amide resins, polyether ester resins, acrylic resins, polyurethane resins Examples thereof include resins, polycarbonate resins, and polyvinyl chloride resins. Among them, especially from polyester resins, polyolefin resins, polyamide resins, acrylic resins, or mixtures thereof because of the variety of monomer types to be copolymerized and the ease of adjusting the material properties. It is preferably formed mainly from a selected thermoplastic resin. In particular, polyester resins such as polyethylene terephthalate, polyethylene-2, 6-naphthalate, polypropylene terephthalate, and polybutylene terephthalate are more preferable in terms of mechanical strength, heat resistance, and the like. By using a polyester resin as a matrix resin, high mechanical strength can be imparted when a film is formed while maintaining high uncoloration. It is also inexpensive.

  Here, the crystallization enthalpy can be adjusted by appropriately copolymerizing the monomer species of the resin constituting the crystalline resin (A). For example, the crystallization enthalpy can be increased by introducing an aromatic skeleton such as a benzene ring, naphthalene ring, anthracene ring, or pyrene ring into the main skeleton, or adding a crystallization accelerator or the like to the resin. In addition, the crystallization enthalpy can be reduced by introducing an alicyclic skeleton such as a cyclohexane skeleton or a norbornene skeleton, an umbrella skeleton such as a bisphenol-A skeleton, a spiroglycol skeleton, or bisphenoxyethanol fluorene into the main skeleton. .

  The crystallization enthalpy can also be adjusted by introducing a plasticizer or a crosslinking agent. For example, the crystallization enthalpy can be lowered as the amount of plasticizer or cross-linking agent added increases. By adding these appropriately, a resin that satisfies the above-mentioned condition range may be used.

  In the white film of the present invention, the resin species constituting the matrix may be a mixture of a crystalline resin and an amorphous resin. In that case, when the total resin (including resin particles) constituting the S layer is 100% by weight, the crystalline resin (A) constituting the matrix of the S layer (if there are a plurality of crystalline resins, all The ratio of the total weight of the crystalline resin) is preferably 50% by weight or more from the viewpoint of heat resistance and mechanical strength.

  In the white film of the present invention, the incompatible resin (B) is a resin that is not compatible with at least the matrix made of the crystalline resin (A) and is finely dispersed in the matrix. In the white film of the present invention, voids (bubbles) are formed using the resin as a core by finely dispersing an incompatible resin in the matrix and stretching.

Here, in the white film of the present invention, the melting point η1 (Pa · s) of the crystalline resin (A) at the melting point Tm + 20 ° C. and the shear rate of 200 sec ⁻¹ of the crystalline resin (A) and the incompatible property. The melt viscosity η2 (Pa · s) of the resin (B) has a relationship of (1) −0.1 ≦ log ₁₀ (η2 / η1) ≦ 0.45 . Here, the melt viscosity η1 of the crystalline resin (A) and the melt viscosity η2 of the incompatible resin (B) are values obtained by a method according to JIS K-7199, and It is a value calculated | required in the procedure of 1) -3).
1) About each of this crystalline resin (A) and incompatible resin (B), when it has hydrolyzability, it dries so that a moisture content may be 50 ppm or less.
2) Using the resin of 1), the melt viscosity is measured at a temperature of melting point Tm + 20 ° C. of the crystalline resin (A) at at least three different shear rates.
3) The obtained value is logarithmically plotted with the shear rate on the horizontal axis and the melt viscosity on the vertical axis, and a power approximation curve is obtained from the obtained plot.
4) Obtain the melt viscosity at a shear rate of 200 sec ⁻¹ from the obtained power approximation curve.

  Here, as a method for drying the resin, a publicly known method such as a hot air oven, a hot plate, heat drying using infrared rays, vacuum drying, freeze drying, or a combination thereof may be used. In addition, after drying, in order to prevent moisture absorption, drying is performed immediately before measurement, and measurement is performed immediately after the completion of drying. If measurement immediately after drying is impossible, the sample is stored in a desiccator, storage, etc. under conditions that do not absorb moisture, such as dry conditions, dry nitrogen conditions, and vacuum conditions, until immediately before measurement.

  Moreover, melting | fusing point Tm of crystalline resin (A) is melting | fusing point Tm in the temperature rising process (temperature rising rate: 20 degree-C / min) obtained by differential scanning calorimetry (henceforth, DSC), JIS K-7121 ( 1999) at a heating rate of 20 ° C./min from 25 ° C. to 300 ° C. (1stRUN), held in that state for 5 minutes, then rapidly cooled to 25 ° C. or lower, and again from room temperature to 20 ° C. The melting point Tm of the crystalline resin is determined by the temperature at the peak top in the crystal melting peak in the 2ndRUN differential scanning calorimetry chart obtained by raising the temperature to 300 ° C. at a temperature raising rate of ° C./min.

In the white film of the present invention , −0.1 ≦ log ₁₀ (η2 / η1) ≦ 0.45, particularly preferably 0 ≦ log ₁₀ (η2 / η1) ≦ 0.40. In the white film of the present invention, when log ₁₀ (η2 / η1) exceeds 0.55, the viscosity of the incompatible resin (B) is too high, and sufficient shearing is applied to the incompatible resin (B) during kneading. It is difficult to apply it and it may be difficult to reduce the dispersion diameter. When log ₁₀ (η2 / η1) is less than −0.3, the viscosity of the incompatible resin (B) is too low and the incompatible resin (B) is kneaded into the matrix containing the crystalline resin (A). This is not preferable because it becomes difficult. In the white film of the present invention, it is possible to achieve both kneadability and fine dispersibility by controlling within the above range.

In the white film of the present invention, the crystalline resin (A) has a melting point Tm + 20 ° C., a shear rate of 200 sec ⁻¹ , the melt viscosity η1 (Pa · s) of the crystalline resin (A) and the incompatible resin ( The melt viscosity η2 (Pa · s) of B) has a relationship of 0.95 ≦ log ₁₀ (η2) / log ₁₀ (η1) ≦ 1.20 . Preferably 0.95 ≦ log ₁₀ (η2) / log ₁₀ (η1) ≦ 1.15. In the white film of the present invention, when log ₁₀ (η2) / log ₁₀ (η1) exceeds 1.3, the viscosity of the incompatible resin (B) is too high, and the incompatible resin (B) is kneaded during kneading. Since it becomes difficult to apply sufficient shear and it may be difficult to reduce the dispersion diameter, it is not preferable. When log ₁₀ (η2) / log ₁₀ (η1) is less than 0.5, the viscosity of the incompatible resin (B) is too low, and the incompatible resin (B) is converted into a matrix containing the crystalline resin (A). Since kneading itself becomes difficult, it is not preferable. In the white film of the present invention, by controlling log ₁₀ (η2) / log ₁₀ (η1) within the above range, both kneadability and fine dispersibility can be achieved.

In the white film of the present invention, it is possible to achieve both kneadability and fine dispersibility by controlling log ₁₀ (η2 / η1) and log ₁₀ (η2) / log ₁₀ (η1) to a specific range. It becomes.

Here, in the white film of the present invention, the melting viscosity Tm + 20 ° C. of the crystalline resin (A) and the melt viscosity η1 (Pa · s) of the crystalline resin (A) at a shear rate of 200 sec ⁻¹ and the incompatible resin. The melt viscosity η2 (Pa · s) difference η2−η1 of (B) is preferably −300 to 1000 Pa · s.

  More preferably, η2−η1 is −200 to 800 Pa · s, more preferably −100 to 700 Pa · s, and particularly preferably −50 to 600 Pa · s. In the white film of the present invention, when η2−η1 exceeds 1000 Pa · s, the viscosity of the incompatible resin (B) is too high to make it difficult to finely disperse in the matrix, or the crystalline resin ( Since the viscosity of A) is too low and the mechanical strength of the formed sheet may be lowered, it is not preferable. On the other hand, if η2−η1 is less than −300 Pa · s, the viscosity of the incompatible resin (B) is too low, and it becomes difficult to knead itself into the matrix containing the crystalline resin (A). Since the viscosity of (A) is too high, extrusion becomes difficult, and it may be difficult to form a sheet. In the white film of the present invention, the difference η2−η1 between η1 of the crystalline resin (A) and the melt viscosity η2 of the incompatible resin (B) is set to −300 to 1000 Pa · s, so that kneadability, Dispersibility, film-forming property, and mechanical strength of the formed film can be compatible.

  In the white film of the present invention, the crystalline resin (A) preferably has a melt viscosity η1 of 50 to 3000 Pa · s. More preferably, it is 80-2000 Pa.s, More preferably, it is 100-1000 Pa.s. In the white film of the present invention, when η1 exceeds 3000 Pa · s, it is not preferable because the polymerization becomes difficult or even if the polymerization is possible, the viscosity of the resin is too high and the extrusion becomes difficult. Further, when η2 is less than 50 Pa · s, shearing is less likely to occur during kneading, and coarse particles are likely to remain, and air bubbles are likely to be bitten during film formation, making it difficult to form a sheet or forming a sheet. However, the mechanical strength may decrease, which is not preferable. In the white film of the present invention, when the crystalline resin (A) has a melt viscosity η1 of 50 to 3000 Pa · s, both the film-forming property and the mechanical strength of the white film can be achieved.

  Further, when the melt viscosity η1 range of the above-mentioned crystalline resin (A) is 300 Pa · s or more, the entanglement of the molecular chain becomes stronger and the film-forming property is less torn during film formation, and the film-forming property is white. A film can be formed. Moreover, since internal stress at the time of extending | stretching will become difficult to remain when melt viscosity shall be 400 Pa.s or less, it can be set as a white film with a lower thermal contraction rate.

  The incompatible resin (B) preferably has a melt viscosity η2 of 10 to 2000 Pa · s. More preferably, it is 20-1500 Pa.s, More preferably, it is 20-1000 Pa.s, Most preferably, it is 50-800 Pa.s. When η2 exceeds 2000 Pa · s in the white film of the present invention, the crystalline resin (A) has a crystalline resin (A) in order to bring the melt viscosity η1 and the crystalline resin (B) η2 into the above-described viscosity relationship. It is necessary to increase the viscosity of A), and the polymerization is difficult. Even if the polymerization is possible, the viscosity of the resin is too high and extrusion may be difficult. When η2 is less than 10 Pa · s, in order to satisfy the relationship between the above-described melt viscosity η1 of the crystalline resin (A) and the crystalline resin (B) η2, the viscosity of the crystalline resin (A) is set to It is necessary to make it low, and it becomes easy to bite bubbles at the time of film formation, and even if it becomes difficult to form a sheet or even if it can be made into a sheet, its mechanical strength may be lowered, which is not preferable. The white film of this invention WHEREIN: By making melt viscosity (eta) 2 of this incompatible resin (B) into 10-2000 Pa.s, the film forming property and mechanical strength of a white film can be made more compatible.

  As the incompatible resin (B) contained in the white film of the present invention, both a crystalline resin and an amorphous resin can be used as long as the above requirements are satisfied. Here, the crystalline resin is the same as described in the definition of the crystalline resin (A), in accordance with JIS K7122 (1999), at a temperature rising rate of 20 ° C./min. Heat at a rate of temperature increase of 1 ° C / min (1stRUN), hold for 5 minutes in that state, then rapidly cool to 25 ° C or less, and then increase the temperature from room temperature to 300 ° C at a rate of 20 ° C / min. In the differential scanning calorimetry chart of 2ndRUN obtained in this way, it is a resin in which an exothermic peak accompanying crystallization is observed. More specifically, a resin having a crystallization enthalpy ΔHcc of 1 J / g or more determined from the area of the exothermic peak is defined as a crystalline resin. An amorphous resin is a resin in which an exothermic peak accompanying crystallization is not observed, or even if it is observed, the crystallization enthalpy is less than 1 J / g.

  Here, when the incompatible resin (B) is an amorphous resin (B1), the glass transition temperature Tg1 of the incompatible resin (B1) is preferably 170 ° C. or higher. The glass transition temperature Tg1 of the amorphous resin (B1) is a glass transition temperature Tg1 in a temperature rising process (temperature rising rate: 20 ° C./min) obtained by differential scanning calorimetry (hereinafter referred to as DSC). JIS K -7121 (1999), the resin was heated from 25 ° C. to 300 ° C. at a rate of temperature increase of 20 ° C./min (1stRUN) at a rate of temperature increase of 20 ° C./min, held in that state for 5 minutes, then In the 2ndRUN differential scanning calorimetry chart obtained by rapidly cooling to 25 ° C. or lower and again raising the temperature from room temperature to 300 ° C. at a temperature rising rate of 20 ° C./min. The value obtained from the point where the straight line equidistant in the vertical axis direction from the extended straight line of each base line and the curve of the step-like change part of the glass transition intersect. More preferably, the glass transition temperature Tg1 is 180 ° C. or higher, more preferably 185 ° C. or higher.

  In the white film of the present invention, if the glass transition temperature Tg1 of the amorphous resin (B1) is less than 170 ° C., when the film is subjected to heat treatment in order to impart dimensional stability, it is an incompatible material that is a core material. In some cases, the resin (B1) is deformed, and as a result, bubbles formed using the resin as a nucleus are reduced or disappeared, and the reflection characteristics are deteriorated. Further, if the heat treatment temperature is lowered to maintain the reflection characteristics, the dimensional stability of the film may be lowered in that case, which is not preferable. In the white film of the present invention, by setting the glass transition temperature Tg1 of the amorphous resin (B1) to 170 ° C. or higher, it is possible to achieve both high reflectivity and dimensional stability.

  In the white film of the present invention, the upper limit of the glass transition temperature of the amorphous resin (B1) is not particularly defined, but preferably the melting point of the crystalline resin (A) is Tm−5 ° C. or less, more preferably Tm−. 10 degrees C or less, More preferably, Tm-20 degrees C or less is good. In the white film of the present invention, when the glass transition temperature Tg1 of the amorphous resin (B1) exceeds Tm−5 ° C., the amorphous resin (B1) is sufficiently incompatible with the crystalline resin (A) serving as a matrix. This is because it is considered that B1) is not softened and fine dispersion is not promoted.

  Moreover, in the white film of this invention, when incompatible resin (B) is crystalline resin (B2), it is preferable that melting | fusing point Tm2 of this crystalline resin (B2) is 170 degreeC or more. The melting point Tm2 of the crystalline resin (B2) is the melting point Tm in the temperature rising process (temperature rising rate: 20 ° C./min), and from 25 ° C. to 300 ° C. by a method based on JIS K-7121 (1999). Heat at a heating rate of 20 ° C / min (1stRUN), hold in that state for 5 minutes, then rapidly cool to 25 ° C or less, and again increase from room temperature to 300 ° C at a heating rate of 20 ° C / min. The melting point Tm2 of the crystalline resin (B2) is determined by the temperature of the peak top in the crystal melting peak in the 2ndRUN differential scanning calorimetry chart obtained. More preferably, the crystalline resin (B2) has a melting point Tm2 of 180 ° C. or higher, more preferably 185 ° C. or higher.

  In the white film of the present invention, if the melting point Tm2 of the crystalline resin (B2) is less than 170 ° C., the incompatible resin (B2) which is a core material when the film is subjected to heat treatment in order to impart dimensional stability. May melt, and as a result, bubbles formed by using the core as a nucleus may be reduced or disappeared, and the reflection characteristics may be deteriorated. Further, if the heat treatment temperature is lowered to maintain the reflection characteristics, the dimensional stability of the film may be lowered in that case, which is not preferable. In the white film of the present invention, by setting the melting point Tm2 of the crystalline resin (B2) to 170 ° C. or higher, it is possible to achieve both high reflectivity and dimensional stability.

  In the white film of the present invention, the upper limit of the melting point Tm2 of the crystalline resin (B2) is not particularly defined, but preferably the melting point of the crystalline resin (A) is Tm-5 ° C. or less, more preferably Tm-10. C. or lower, more preferably Tm-20.degree. C. or lower. In the white film of the present invention, when the melting point Tm2 of the crystalline resin (B2) exceeds Tm-5 ° C., the incompatible resin (B2) is sufficiently mixed with the crystalline resin resin (A) serving as a matrix. This is because it is considered that fine dispersion is not promoted without softening.

  In the white film of the present invention, the incompatible resin (B) preferably satisfies the above-mentioned requirements. Specific examples thereof include copolymerized polyester resins, polyethylene, polypropylene, polybutene, polymethylpentene, cyclopentadiene, and the like. Linear, branched or cyclic polyolefin resin, polyamide resin, polyimide resin, polyether resin, polyesteramide resin, polyetherester resin, acrylic resin, polyurethane resin, polycarbonate Resin, polyvinyl chloride resin, polyacrylonitrile, polyphenylene sulfide, polystyrene, fluorine resin and the like. Among them, especially from polyester resins, polyolefin resins, polyamide resins, acrylic resins, or mixtures thereof because of the variety of monomer types to be copolymerized and the ease of adjusting the material properties. It is preferably formed mainly from a selected thermoplastic resin. These incompatible resins may be a homopolymer or a copolymer, and two or more incompatible resins may be used in combination.

  Specifically, when a polyester resin is used as the matrix, the incompatible resin (B) includes a polyolefin resin, a polyamide resin, a polyimide resin, a polyether resin, a polyesteramide resin, and a polyether. Preferred examples include ester resins, acrylic resins, polyurethane resins, polycarbonate resins, and polyvinyl chloride resins. Among these, the incompatible resin (B) includes linear, branched or cyclic polyolefin resins such as polyethylene, polypropylene, polybutene, polymethylpentene, cyclopentadiene, and poly (meth) acrylate. An acrylic resin such as polystyrene, a fluorine resin, or the like is preferably used. These incompatible resins may be a homopolymer or a copolymer, and two or more incompatible resins may be used in combination. Among these, a polyolefin-based resin having a small surface tension is preferably used in that it has excellent void formability. Specifically, when the incompatible resin (B) contained in the white film of the present invention is a crystalline resin (B2), polypropylene and polymethylpentene are preferably used. Polymethylpentene has a relatively large difference in surface tension with polyester and is excellent in void formation, not only has a large effect of forming bubbles per added amount, but also has a high melting point, so that deformation due to heat treatment is unlikely to occur. It is particularly preferable as the crystalline resin (B2) because it can be sufficiently subjected to heat treatment during production, and as a result, the mechanical strength and dimensional stability of the formed film can be improved.

  Here, as polymethylpentene, those containing a derivative unit from 4-methylpentene-1 in the molecular skeleton are preferably 80 mol% or more, more preferably 85 mol% or more, and particularly preferably 90 mol% or more. . Examples of other derived units include hydrocarbons having 6 to 12 carbon atoms other than ethylene units, propylene units, butene-1 units, 3-methylbutene-1, or 4-methylpentene-1. The polymethylpentene may be a homopolymer or a copolymer. Further, a plurality of polymethylpentenes having different compositions and melt viscosities may be used, or other olefinic resins and other resins may be used in combination.

Moreover, when the incompatible resin (B) used for the white film of the present invention is a crystalline resin (B1), a cyclic olefin copolymer is particularly preferably used. The cyclic olefin copolymer is a copolymer composed of at least one cyclic olefin selected from the group consisting of cycloalkene, bicycloalkene, tricycloalkene and tetracycloalkene, and linear olefin such as ethylene and propylene. is there. Representative examples of such cyclic olefins include bicyclo [2,2,1] hept-2-ene, 6-methylbicyclo [2,2,1] hept-2-ene, and 5,6-dimethylbicyclo [2,2 , 1] hept-2-ene, 1-methylbicyclo [2,2,1] hept-2-ene, 6-ethylbicyclo [2,2,1] hept-2-ene, 6-n-butylbicyclo [ 2,2,1] hept-2-ene, 6-i-butylbicyclo [2,2,1] hept-2-ene, 7-methylbicyclo [2,2,1] hept-2-ene, tricyclo [ 4,3,0,1 ^2.5 ] -3-decene, 2-methyl-tricyclo [4,3,0,1 ^2.5 ] -3-decene, 5-methyl-tricyclo [4,3,0,1 ^2.5 ]- 3-decene, tricyclo [4,4,0,1 ^2.5] -3-decene, 10-methyl - tri There are black [4,4,0,1 ^2.5] -3-decene.

  In particular, bicyclo [2,2,1] hept-2-ene (norbornene) and its derivatives are preferable in terms of productivity, transparency, and high Tg.

  In the white film of the present invention, when the incompatible resin (B) is an amorphous resin (B1), polymethylpentene, polypropylene, polystyrene and the like are conventionally used by using the cyclic olefin copolymer as described above. It becomes possible to finely disperse in the film more than the incompatible resin that has been developed, and as a result, a large number of gas-solid interfaces can be formed in the thickness direction of the film, which cannot be achieved with a conventional white film. High reflection characteristics, whiteness, and concealment can be obtained. In particular, when it is used for a reflective film for liquid crystal display, the light use efficiency can be increased, and as a result, a high brightness improvement effect that cannot be obtained with a conventional white film can be obtained.

  Further, in order to control the glass transition temperature Tg1 of the amorphous resin (B1) within the above-mentioned range, for example, the content of the cyclic olefin component in the cyclic olefin copolymer is increased, and a linear olefin component such as ethylene is used. The content of can be reduced. Specifically, the cyclic olefin component is 60 mol% or more, and the content of linear olefin components such as ethylene is preferably less than 40 mol%. More preferably, the cyclic olefin component is 70 mol% or more, the content of the linear olefin component such as ethylene is less than 30 mol%, more preferably the cyclic olefin component is 80 mol% or more, and the linear chain such as ethylene. The content of the olefin component is less than 20 mol%. Particularly preferably, the cyclic olefin component is 90 mol% or more, and the content of linear olefin components such as ethylene is less than 10 mol%. By setting it as this range, the glass transition temperature of a cyclic olefin copolymer can be raised to the glass transition temperature Tg1 of the above-mentioned range.

  The linear olefin component is not particularly limited, but an ethylene component is preferable from the viewpoint of reactivity.

  Furthermore, the cyclic olefin component is not particularly limited, but bicyclo [2,2,1] hept-2-ene (norbornene) and its derivatives are preferable from the viewpoint of productivity, transparency, and high Tg.

  In addition to the above two components, other copolymerizable unsaturated monomer components can be copolymerized as necessary within the range not impairing the object of the present invention. Examples of the copolymerizable unsaturated monomer include propylene, 1-butene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene and 1-hexadecene. , 1-octadecene, 1-eicosene and the like, an α-olefin having 3 to 20 carbon atoms, cyclopentene, cyclohexene, 3-methylcyclohexene, cyclooctene, 1,4-hexadiene, 4-methyl-1,4-hexadiene, 5-methyl-1,4-hexadiene, 1,7-octadiene, dicyclopentadiene, 5-ethylidene-2-norbornene, 5-vinyl-2-norbornel, tetracyclododecene, 2-methyltetracyclododecene, 2 -Ethyltetracyclododecene and the like can be exemplified.

  In the white film of the present invention, the above-mentioned incompatible resin (B) is preferably contained in an amount of 5 to 50% by weight when the total of all materials constituting the S layer is 100% by weight. Preferably, the addition amount of the incompatible resin (B) is 10% by weight or more, more preferably 15% by weight or more, and further preferably 20% by weight or more. In the white film of the present invention, when the addition amount of the incompatible resin (B) is less than 5% by weight, the whiteness and light reflection characteristics may be inferior. On the other hand, if the total weight of all materials constituting the S layer exceeds 50% by weight, the strength of the film is lowered and breakage during stretching may easily occur. By setting the content within this range, sufficient whiteness, reflectivity, and lightness can be exhibited.

  In the present invention, when the crystalline resin (A) is a polyester, a copolymerized polyester resin (C) obtained by introducing a copolymerization component into the crystalline resin (A) may be contained as a matrix. In this case, the amount of the copolymer component is not particularly limited, but from the viewpoints of transparency, moldability, etc., and from the viewpoint of amorphousization described below, both the dicarboxylic acid component and the diol component are preferably 1 to It is 70 mol%, More preferably, it is 10-40 mol%.

  Moreover, it is one of the preferable aspects in the white film of this invention to use the polyester which became amorphous by copolymerization as copolymer polyester resin (C). Preferred examples of the amorphous polyester include a copolymer polyester resin in which the main component of the diol component is an alicyclic glycol, and a copolymer polyester resin in which the acid component is isophthalic acid. Particularly, cyclohexane dimethanol, which is a kind of alicyclic glycol, is used as the diol component, and the copolymerized amorphous polyester has transparency and moldability and the effect of fine dispersion of the incompatible resin (B) described later. From this point, it can be preferably used. In that case, it is preferable from a viewpoint of amorphization that the cyclohexane dimethanol component of the diol component of copolymerized amorphous polyester resin shall be 30 mol% or more. Among them, cyclohexane dimethanol copolymerized polyethylene terephthalate in which 30 to 40 mol% of the diol component is cyclohexanedimethanol, 60 to 70 mol% of the diol component is ethylene glycol, and terephthalic acid is used as the dicarboxylic acid component. Is particularly preferred.

  By adding such a copolymerized amorphous polyester, there is an effect that the dispersion of the incompatible resin (B) in the matrix resin is further stabilized and finely dispersed. Although the detailed reason which this effect expresses is unknown, by this, many bubbles can be generated in a film, and as a result, high reflectivity, high whiteness, and lightness can be achieved. Moreover, stretchability and film forming property can be improved by adding such amorphous polyester.

  In the white film of the present invention, the content of the copolymer resin (C) is 5% by weight to 50% by weight with respect to 100% of the total resin (including resin particles) constituting the matrix of the S layer. Is preferably less than. More preferably, it is 10 to 40 weight%, More preferably, it is 10 to 35 weight%. If the content of the copolymer resin (C) contained in the matrix is less than 10% by weight, it may be difficult to finely disperse the incompatible resin (B) in the matrix. Further, when the content of the copolymer resin (C) exceeds 50% by weight, the heat resistance is lowered, and when the heat treatment of the film is performed in order to impart dimensional stability, the matrix is softened. It may decrease or disappear and the reflection characteristics may deteriorate. Further, if the heat treatment temperature is lowered to maintain the reflection characteristics, the dimensional stability of the film may be lowered in that case, which is not preferable. In the white film of the present invention, the dispersion effect of the incompatible components described above is controlled by controlling the addition amount of the total resin constituting the matrix (copolymer resin (C) with respect to 100 wt% including the resin particles) to the above range. As a result of maintaining the film-forming properties and mechanical properties while fully exhibiting the above, it is possible to achieve both high reflectivity and dimensional stability.

  In the white film of the present invention, in order to further finely disperse the incompatible resin (B) in the matrix, in addition to the above-described crystalline resin (A) and copolymer resin (C), a dispersing agent ( It is preferred to add D).

  By adding the dispersant (D), it becomes possible to further reduce the dispersion diameter of the incompatible resin (B), and as a result, the flat bubbles generated by stretching can be further refined, resulting in the film This is because whiteness, reflectivity, and lightness can be improved.

  The type of the dispersant (D) is not particularly limited, but when the crystalline resin (A) is a polyester resin, an olefin resin having a polar group such as a carboxyl group or an epoxy group or a functional group reactive with the polyester. These polymers or copolymers, diethylene glycol, polyalkylene glycol, surfactants, thermal adhesive resins, and the like can be used. Of course, these may be used alone or in combination of two or more.

  Of these, a polyester-polyalkylene glycol copolymer (D1) comprising a polyester component and a polyalkylene glycol component is particularly preferred.

  In this case, the polyester component is preferably a polyester component comprising an aliphatic diol part having 2 to 6 carbon atoms and a terephthalic acid and / or isophthalic acid part. Moreover, as a polyalkylene glycol component, components, such as polyethylene glycol, polypropylene glycol, polytetramethylene glycol, are preferable.

  Particularly preferred combinations are those using polyethylene terephthalate or polybutylene terephthalate for the polyester component and polyethylene glycol or polytetramethylene glycol for the polyalkylene glycol component. In particular, a combination of polybutylene terephthalate for the polyester component, polytetramethylene glycol for the polyalkylene glycol component, or a combination of polyethylene terephthalate for the polyester component and polyethylene glycol for the polyalkylene glycol component is particularly preferred. preferable.

  The addition amount of the dispersant (D) used in the present invention is not particularly limited, but when the total resin (including resin particles) constituting the matrix of the S layer is 100% by weight, it is 0.1 to 0.1%. 30% by weight is preferable, more preferably 2 to 25% by weight, and still more preferably 5 to 20% by weight. When the addition amount is less than 0.1% by weight, the effect of refining the bubbles may be reduced, which is not preferable. In addition, when the amount added is more than 30% by weight, the heat resistance is lowered, and the matrix is softened when heat-treating the film to give dimensional stability, and as a result, bubbles are reduced or eliminated. As a result, the reflection characteristics may deteriorate. Further, if the heat treatment temperature is lowered to maintain the reflection characteristics, the dimensional stability of the film may be lowered in that case, which is not preferable. In addition, problems such as a decrease in production stability and an increase in cost may occur, which is not preferable. In the white film of the present invention, by controlling the addition amount of the dispersant with respect to all matrix components within the above range, the film forming property and As a result of maintaining the mechanical characteristics, it is possible to achieve both high reflectivity and dimensional stability. Moreover, since problems such as a decrease in production stability and an increase in cost may occur, this is not preferable.

  In the incompatible resin used in the present invention, the white film of the present invention includes, as necessary, appropriate additives in an amount that does not impair the effects of the present invention, for example, heat stabilizer, oxidation resistance. Stabilizers, UV absorbers, UV stabilizers, organic lubricants, organic fine particles, fillers, nucleating agents, dyes, dispersants, coupling agents and the like may be blended.

  The white film of the present invention is prepared by melting and kneading the crystalline resin (A), the incompatible resin (B), the copolymer resin (C), and the dispersant (D), and then processing the sheet. Formed by peeling at the interface between the crystalline resin (A) that is a matrix and the incompatible resin (B) by stretching uniaxially or biaxially, an incompatible resin (B) (hereinafter, It is also a white film having voids that are also referred to as resin particles.

  In the white film of the present invention, the bubbles may be independent bubbles or may be two-dimensional or three-dimensional continuous bubbles. The shape of the bubble is not particularly limited, but the whiteness and light reflectivity of the film reflect the light incident on the film at the internal gas-solid interface (the gas-solid interface consisting of bubbles and matrix resin or resin particles). Therefore, it is preferable to form a large number of gas-solid interfaces in the film thickness direction. In order to form a large number of gas-solid interfaces in the film thickness direction, the cross-sectional shape of the bubbles is preferably a circular shape or an elliptical shape extending in the film surface direction.

  In the white film of the present invention, the number average particle diameter Dn of the resin particles contained in the S layer is preferably 1.5 μm or less. The number average particle diameter Dn of the resin particles here is the diameter of the resin particles observed in the cross section of the S layer of the white film. If the shape is not a perfect circle, the value is converted to a perfect circle of the same area. That is. Here, the number average particle diameter Dn can be determined by the following procedures 1) to 3).

  1) First, a microtome is used to cut the film cross section without crushing it in the thickness direction, and an enlarged observation image is obtained using a scanning electron microscope. At this time, the cutting is performed in a direction parallel to the film TD direction (lateral direction).

2) Next, for each resin particle having a particle diameter in the range of 50 nm to 10 μm observed in the cross section of the S layer in the image, the cross-sectional area S is obtained, and the particle diameter d obtained by the following formula (1) D = 2 × (S / π) ^1/2 (1)
(Where π is the circumference).

3) Dn is calculated | required by following formula (2) using the obtained particle diameter d and the number n of resin particles.
Dn = Σd / n (2)
(Where Σd is the sum of the particle diameters of the resin particles in the observation plane, and n is the total number of resin particles in the observation plane).

4) The above 1) to 3) are carried out by changing the location at five locations, and the average value thereof is taken as the number average particle diameter Dn of the resin particles. Note that the above evaluation is performed in an area of 2500 μm ² or more per observation point.

  More preferably, the number average particle diameter Dn determined by the above method is 1.2 μm or less, and more preferably 1.0 μm or less. In the white film of the present invention, when the number average particle diameter Dn of the resin particles exceeds 1.5 μm, it becomes difficult to contain a large number of bubbles having the resin particles as the core in the white film, or coarse bubbles are formed. As a result, it becomes difficult to form a large number of gas-solid interfaces in the film thickness direction. Therefore, the whiteness as a white film, light reflection characteristics, and lightness are inferior, and even if incorporated in a liquid crystal display device, the luminance characteristics may be inferior. In the white film of the present invention, by setting the number average particle diameter Dn of the resin particles contained in the S layer to 1.5 μm or less, high reflection characteristics as a white film can be obtained.

Further, the white film of the present invention preferably contains 0.05 or more / μm ^{2 of the} resin particles in the S layer. It is the number obtained by the measurement method described later. More preferably, it is 0.08 pieces / μm ² or more, further preferably 0.10 pieces / μm ² or more, particularly preferably 0.11 pieces / μm ² or more, and most preferably 0.12 pieces / μm ² . In the white film of the present invention, if the resin particles are less than 0.05 / μm ² , it is difficult to contain a large number of air bubbles having the resin particles as a core in the white film, or coarse air bubbles are generated. As a result of the formation, it is difficult to form a large number of gas-solid interfaces in the film thickness direction. Therefore, the whiteness as a white film, light reflection characteristics, and lightness are inferior, and even if incorporated in a liquid crystal display device, the luminance characteristics may be inferior. In the white film of the present invention, when the resin particles in the S layer are contained in an amount of 0.05 / μm ² or more, high reflection characteristics as a white film can be obtained.

  In the white film of the present invention, the ratio of the number of resin particles having a particle size of 2 μm or more among the resin particles contained in the S layer is 15% or less with respect to the total number of resin particles in the S layer. It is preferable that More preferably, it is 12% or less, more preferably 10% or less, and particularly preferably 8% or less. In the present invention, if the ratio of the number of the resin particles having a particle diameter of 2 μm or more exceeds 15%, it is difficult to contain a large number of bubbles having the resin particles as a nucleus in the white film, or coarse bubbles. As a result, it becomes difficult to form a large number of gas-solid interfaces in the film thickness direction. Therefore, the whiteness as a white film, light reflection characteristics, and lightness are inferior, and even if incorporated in a liquid crystal display device, the luminance characteristics may be inferior. In the white film of the present invention, among the resin particles contained in the film, by controlling so that the number of the resin particles having a particle diameter of 2 μm or more is 15% or less, high reflection as a white film is achieved. Characteristics can be obtained.

  In the white film of the present invention, the ratio Dv / Dn of the volume average particle diameter Dv and the number average particle diameter Dn of the resin particles contained in the S layer is preferably 1.7 or less. Here, the ratio Dv / Dn of the volume average particle diameter Dv and the number average particle diameter Dn of the resin particles is a value obtained by using the volume average particle diameter Dv obtained by the following procedures 1) to 3). That is.

  1) First, a microtome is used to cut the film cross section without crushing it in the thickness direction, and an enlarged observation image is obtained using a scanning electron microscope. At this time, the cutting is performed in a direction parallel to the film TD direction (lateral direction).

2) Next, for each resin particle observed in the cross section of the S layer in the image, the cross sectional area S is obtained, and the particle diameter d obtained by the following formula (3) is obtained. D = 2 × (S / Π) ^1/2 (3)
(Where π is the circumference).

3) Using the obtained particle diameter d, obtain Dv in the following formula (4).
Dv = Σ [4 / 3π × (d / 2) ³ × d] / Σ [4 / 3π × (d / 2) ³ ] (4)
(Where π is the circumference).

4) The above 1) to 3) are carried out at five locations, and the average value thereof is taken as the volume average particle diameter Dv of the resin particles. Note that the above evaluation is performed in an area of 2500 μm ² or more per observation point.

  Dv / Dn can be obtained by determining the volume average particle diameter Dv and determining the ratio Dv / Dn to the aforementioned number average particle diameter Dn. Dv / Dn obtained here is a value representing the spread of the particle size of the resin particles, and the larger the value, the larger the spread of the particle size distribution of the resin particles. The theoretical lower limit is 1.0, which means complete monodispersion. More preferably, Dv / Dn is 1.6 or less, further preferably 1.5 or less, and particularly preferably 1.4 or less. In the white film of the present invention, when Dv / Dn exceeds 1.7, coarse bubbles are formed in the white film. As a result, it is difficult to uniformly form bubbles with the resin particles as the core, and the film It becomes difficult to form a large number of gas-solid interfaces in the thickness direction. In the white film of the present invention, by setting the ratio Dv / Dn of the volume average particle diameter Dv and the number average particle diameter Dv of the resin particles contained in the S layer to 1.7 or less, uniform bubbles are formed inside the film. As a result, high reflection characteristics as a white film can be obtained.

  The white film of the present invention may be a single white film consisting of only the S layer, but a layer different from the A layer (B) on at least one side of the S layer (hereinafter, the S layer may also be referred to as the A layer). It is also a preferred embodiment that the layer is laminated. By laminating layers having such other functional layers, the light diffusibility of reflected light is controlled, high mechanical strength is imparted to the film, film-forming properties are imparted, and other incidental functions are provided. Can have. The laminated structure may be either A layer / B layer or B layer / A layer / B layer.

  In the case where the white film of the present invention has a laminated structure, it is preferable to add various particles to the B layer in order to improve surface slippage and running durability during film formation. At this time, the laminated B layer can contain organic or inorganic fine particles or incompatible resin. Among these, it is particularly preferable to include inorganic fine particles from the viewpoints of film winding property, long-term film-forming stability, stability over time, and improvement of optical characteristics. Here, since inorganic particles have a larger absorption or the like than resin particles or the like, if they are used in a large amount for the entire film or the main layer (A layer), it is difficult to obtain high reflection characteristics due to the absorption effect. However, by forming the B layer thinly on the surface, various characteristics can be imparted while suppressing absorption as much as possible. Examples of inorganic fine particles include calcium carbonate, magnesium carbonate, zinc carbonate, titanium oxide, zinc oxide (zinc white), antimony oxide, cerium oxide, zirconium oxide, tin oxide, lanthanum oxide, magnesium oxide, barium carbonate, and zinc carbonate. , Basic lead carbonate (lead white), barium sulfate, calcium sulfate, lead sulfate, zinc sulfide, calcium phosphate, silica, alumina, mica, mica titanium, talc, clay, kaolin, lithium fluoride and calcium fluoride, etc. Can do.

  The inorganic fine particles may or may not have bubble forming properties. The bubble-forming property depends on the difference in surface tension with the resin (polyester resin) constituting the matrix, the average particle size of inorganic fine particles, and the cohesiveness (dispersibility). Typical examples of the bubble-forming property include calcium carbonate, barium sulfate, and magnesium carbonate. When bubbles-forming particles are used, bubbles can be included in the laminated layer by stretching in at least one direction during film production, and as a result, reflection characteristics may be improved. preferable. On the other hand, inorganic fine particles having no bubble-forming property are those that whiten the film mainly due to the difference in refractive index from the resin (polyester resin) constituting the matrix, and typical examples thereof include titanium oxide, Zinc sulfide, zinc oxide, cerium oxide, and the like. When these are used, the concealability of the white film can be improved.

  These inorganic fine particles may be used alone or in combination of two or more. Moreover, it may be in the form of a porous or hollow porous material, and may be subjected to a surface treatment in order to improve the dispersibility with respect to the resin within the range not impairing the effects of the present invention.

  The inorganic fine particles used in the present invention preferably have an average particle size in the B layer of 0.05 to 3 μm, more preferably 0.07 to 1 μm. When the average particle diameter of the inorganic fine particles is out of the above range, glossiness or smoothness of the film surface may be deteriorated due to poor uniform dispersion of the inorganic fine particles due to aggregation or the particles themselves.

  Further, the content of the inorganic fine particles in the B layer is not particularly limited, but is preferably 1 to 35% by weight, more preferably 2 to 30% by weight, and even more preferably 3 to 25% by weight. preferable. If the content is less than the above range, it may be difficult to improve the properties such as whiteness and hiding properties (optical density) of the film. Conversely, if the content is more than the above range, the film Not only is the surface smoothness easily lowered, but there are cases in which problems such as film breakage during stretching and generation of powder during post-processing may occur.

  10-500 micrometers is preferable and, as for the thickness of the white film of this invention, 20-300 micrometers is more preferable. Similarly, the thickness of the S layer is preferably 10 to 500 μm, and more preferably 20 to 300 μm. When the thickness is less than 10 μm, it becomes difficult to ensure the flatness of the film, and unevenness in brightness tends to occur when used as a surface light source. On the other hand, when it is thicker than 500 μm, when it is used as a light reflecting film in a liquid crystal display or the like, the thickness may be too large.

  Moreover, when the white film of this invention is a laminated | multilayer film, 1 / 200-1 / 3 are preferable and, as for the thickness ratio of the surface layer part / inner layer (S layer) part, 1 / 50-1 / 4 are more preferable. In the case of a three-layer laminated film of surface layer portion / inner layer (S layer) portion / surface layer portion, the ratio is expressed as the sum of both surface layer portions / inner layer (S layer) portion.

  In order to impart easy adhesion and antistatic properties to the white film of the present invention, various coating liquids are applied using a well-known technique, and a hard coat layer and ultraviolet light resistant to increase impact resistance. A layer having another function (C layer) such as a UV-resistant layer for imparting properties and a flame retardant layer for imparting flame retardancy may be provided.

  Here, as a means for coating, for example, methods such as gravure coating, roll coating, spin coating, reverse coating, bar coating, screen coating, blade coating, air knife coating, and dipping can be used. In particular, a method of coating with a kiss coat using a micro gravure roll is preferable because it is excellent in coating appearance and gloss uniformity. Moreover, when hardening an application layer after application | coating, the hardening method can use a well-known method. For example, thermosetting, a method using active rays such as ultraviolet rays, electron beams, radiation, or a combination of these methods can be applied. At this time, it is preferable to use a curing agent such as a crosslinking agent in combination. Moreover, as a method of providing an application layer, it may be applied at the time of white film production (in-line coating), or may be applied onto the white film after completion of crystal orientation (off-line coating).

  The coating layer (C layer) preferably contains fine particles for improving the slipperiness of the coating layer, imparting blocking resistance, adjusting glossiness, and the like. For example, inorganic fine particles or organic fine particles can be used. Examples of the inorganic fine particles include gold, silver, copper, platinum, palladium, rhenium, vanadium, osmium, cobalt, iron, zinc, ruthenium, praseodymium, chromium, nickel, aluminum, tin, zinc, titanium, tantalum, zirconium, Metal oxides such as antimony, indium, yttrium, lanthanium, etc., metal oxides such as zinc oxide, titanium oxide, cesium oxide, antimony oxide, tin oxide, indium tin oxide, yttrium oxide, lanthanum oxide, zirconium oxide, aluminum oxide, silicon oxide Metal fluoride such as lithium fluoride, magnesium fluoride, aluminum fluoride, cryolite, metal phosphate such as calcium phosphate, carbonate such as calcium carbonate, sulfate such as barium sulfate, other talc and kaolin, etc. The It is possible to have. The organic fine particles are incompatible with the silicone resin, crosslinked fine particles such as crosslinked styrene, crosslinked acrylic, and crosslinked melamine, as well as the thermoplastic resin that constitutes the coating layer. The thermoplastic resin to be used can also be used as fine particles. The particle size (number average particle size) of the organic and / or inorganic particles is preferably 0.05 to 15 μm, and preferably 0.1 to 10 μm. Moreover, as content, 5 to 50 weight% is preferable with respect to the dry weight of the coating layer which has an ultraviolet absorptivity, More preferably, it is 6 to 30 weight%, More preferably, it is 7 to 20 weight%. Setting the particle size of the contained particles in the above range is preferable because it prevents the particles from falling off and adjusts the glossiness of the surface.

  In general, the white film of the present invention preferably has a higher whiteness, and more preferably has a bluish color than yellow. Considering this point, it is preferable to add a fluorescent brightening agent in the white film and / or in the coating layer.

  Commercially available fluorescent whitening agents may be used as appropriate, for example, “Ubitech” (manufactured by Ciba-Gaigi), OB-1, (manufactured by Eastman), TBO (manufactured by Sumitomo Seika Co., Ltd.), “Kecoal” "Kayalite" (manufactured by Nippon Soda Co., Ltd.), "Kayalite" (manufactured by Nippon Kayaku Co., Ltd.), "Lyukopua" EGM (manufactured by Client Japan), etc. can be used. The content of the optical brightener in the film is preferably 0.005 to 1% by weight, more preferably 0.007 to 0.7% by weight, and even more preferably 0.01 to 0.5% by weight. It is particularly preferred. If it is less than 0.005% by weight, the effect is small, and if it exceeds 1% by weight, it may turn yellowish. When the white film is a laminated film, it is more effective to add the fluorescent whitening agent to the surface layer portion.

  Moreover, the white film of this invention may contain the light-resistant agent in the white film and / or the coating layer. The term “light-proofing agent” as used herein refers to a material having ultraviolet absorbing ability. By containing this in a white film and / or a coating layer, a change in color tone due to ultraviolet rays of the film can be prevented. The light stabilizer preferably used is not particularly limited as long as other properties are not impaired, but has excellent heat resistance, good compatibility with the matrix resin, uniform dispersion, and less color and resin and film. It is desirable to select a light-proofing agent that does not adversely affect the reflection characteristics of the light. Examples of such a light-proofing agent include salicylic acid-based, benzophenone-based, benzotriazole-based, cyanoacrylate-based, triazine-based UV absorbers, hindered amine-based UV stabilizers, and the like. Specifically, for example, salicylic acid-based pt-butylphenyl salicylate, p-octylphenyl salicylate, benzophenone-based 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy -5-sulfobenzophenone, 2,2 ', 4,4'-tetrahydroxybenzophenone, bis (2-methoxy-4-hydroxy-5-benzoylphenyl) methane, 2- (2'-hydroxy-5) of benzotriazole series '-Methylphenyl) benzotriazole, 2- (2'-hydroxy-5'-methylphenyl) benzotriazole, 2,2'-methylenebis [4- (1,1,3,3-tetramethylbutyl) -6- (2H benzotriazol-2-yl) phenol], a cyanoacrylate-based ester 2- (4,6-diphenyl-1,3,5-triazin-2-yl) -5-[(hexyl) as the tri-2-cyano-3,3′-diphenyl acrylate) and others and as triazines And oxy] -phenol.

  Examples of the UV stabilizer include hindered amine-based bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, dimethyl succinate 1- (2-hydroxyethyl) -4-hydroxy-2. , 2,6,6-tetramethylpiperidine polycondensate, as well as nickel bis (octylphenyl) sulfide, and 2,4-di-t-butylphenyl-3 ′, 5′-di-t-butyl- Examples include 4′-hydroxybenzoate. Among these light-proofing agents, 2,2 ′, 4,4′-tetrahydroxy-benzophenone, bis (2-methoxy-4-hydroxy-5-benzoylphenyl) methane, and 2,2 ′ are excellent in compatibility with polyester. -Methylenebis [4- (1,1,3,3-tetramethylbutyl) -6- (2Hbenzotriazol-2-yl) phenol] and 2- (4,6-diphenyl-1,3,5-triazine Application of -2-yl) -5-[(hexyl) oxy] -phenol is preferred. The above light resisting agents may be used alone or in combination of two or more.

  The content of the light-proofing agent in the white film of the present invention is preferably 0.05 to 10% by weight, more preferably 0.1 to 5% by weight, and still more preferably based on the layer containing the light-proofing agent. Is 0.15 to 3% by weight. When the light-proofing agent content is less than 0.05% by weight, the light resistance is insufficient, and the color tone changes during long-term storage, and when the light-proofing agent content exceeds 10% by weight. The color of the film may be changed by coloring with a light resistance agent.

  Here, when the white film of the present invention is a single layer, the layer having an ultraviolet absorbing ability may be provided with an ultraviolet absorbing agent in the film to impart the ultraviolet absorbing ability to the entire film. A coating layer (C layer) containing an ultraviolet absorber may be formed on at least one side of the film. In addition, when the white film has a laminated structure, any one of the layer A composed of the white film of the present invention or the layer B provided on the surface layer thereof contains an ultraviolet absorber and imparts an ultraviolet absorbing ability. Alternatively, a coating layer (C layer) containing an ultraviolet absorber may be formed on at least one side of the film. Further, the layer having the ultraviolet absorbing ability may be a single layer or a plurality of layers, but in the case of a plurality of layers, any of the layers is a layer containing an ultraviolet absorber, Preferably, two or more layers are layers containing an ultraviolet absorber from the viewpoint of maintaining weather resistance.

  When the layer having ultraviolet absorbing ability is a white film (A layer) or a surface layer (B layer), the resin constituting the matrix may contain or copolymerize an ultraviolet absorber. Further, when the layer having the ultraviolet absorbing ability is a coating layer (C layer), an ultraviolet absorber is contained in a resin component such as a thermoplastic, thermosetting or active curable resin constituting the coating layer (C layer). May be contained or copolymerized. Moreover, in the case of a coating layer, it is also preferably performed to contain a UV-absorbing monomer having crosslinkability and to form a coating layer by crosslinking after coating.

  Examples of ultraviolet absorbers include, for example, benzophenone-based, benzotriazole-based, triazine-based, cyanoacrylate-based, salicylic acid ester-based, benzoate-based, or inorganic UV-screening agents containing or copolymerized in a resin. It can be obtained by laminating. Among these, when forming the coating layer (C layer), a benzotriazole-based ultraviolet absorber is more preferable.

  As the benzotriazole-based ultraviolet absorber, any of those that become a polymer at the time of addition and those that can be crosslinked with a monomer in the coating and drying step are preferably used. The monomer having a benzotriazole skeleton is not particularly limited as long as it is a monomer having benzotriazole in the basic skeleton and an unsaturated double bond. Preferred monomers include 2- (2′-hydroxy- 5′-acryloyloxyethylphenyl) -2H-benzotriazole, 2- (2′-hydroxy-5′-methacryloxyethylphenyl) -2H-benzotriazole, 2- (2′-hydroxy-3′-tert-butyl) -5'-acryloyloxyethylphenyl) -5-chloro-2H-benzotriazole is preferred. Acrylic monomers and / or oligomers copolymerized with these monomers include alkyl acrylates, alkyl methacrylates, and monomers having crosslinkable functional groups such as carboxyl groups, methylol groups, acid anhydride groups, sulfonic acid groups, amides. Examples thereof include monomers having a group, an amino group, a hydroxyl group, an epoxy group, and the like.

  In the coating layer (C layer) having an ultraviolet absorbing ability preferably used in the white film of the present invention, one or more of the above acrylic monomers and / or oligomers may be copolymerized at an arbitrary ratio. Preferably, methyl methacrylate or styrene is polymerized by 20% by weight or more, more preferably 30% by weight or more of the acrylic monomer, from the viewpoint of the hardness of the laminated film. The copolymerization ratio of the benzotriazole monomer and the acrylic monomer is such that the ratio of the benzotriazole monomer is 10% by weight to 70% by weight, preferably 20% by weight to 65% by weight, more preferably 25% by weight to 60%. It is preferable from the viewpoint of durability and adhesion with a substrate film that the content is not more than% by weight. The molecular weight of the copolymer is not particularly limited, but is preferably 5000 or more, and more preferably 10,000 or more from the viewpoint of durability of the coating layer. The production of the copolymer can be obtained by a method such as radical polymerization, and is not particularly limited. The copolymer is laminated on the base film as an organic solvent or an aqueous dispersion, and the thickness is usually 0.5 to 15 μm, preferably 1 to 10 μm, more preferably 1 to 5 μm. It is particularly preferable in terms of light resistance to be within the range.

  Various additives can be added to the coating layer (C layer) having an ultraviolet absorbing ability in the white film of the present invention within a range not inhibiting the effects of the present invention. As the additive, for example, a fluorescent brightening agent, a crosslinking agent, a heat stabilizer, an antistatic agent, a coupling agent and the like can be used.

  The white film of the present invention has the above-described configuration, but the total light transmittance of the white film is preferably 2.5% or less. More preferably, it is 2.3% or less, More preferably, it is 2.0% or less. In addition, the transmittance | permeability here is the value measured based on JIS-7361 (1997). In the white film of the present invention, by setting the transmittance to 2.0% or less, light leakage to the back surface can be suppressed. As a result, a white film excellent in whiteness and reflection characteristics can be obtained. When used for a display device, a high luminance improvement effect can be obtained.

  The white film of the present invention preferably has a relative reflectance of 100% or more. More preferably, it is 100.5% or more, More preferably, it is 101% or more. Here, the relative reflectance refers to an integrating sphere made of barium sulfate on the inner surface, a spectrophotometer equipped with a 10 ° inclined spacer, and aluminum oxide as a standard white plate, and light was incident at an incident angle of 10 °. Is the relative reflectance when the reflectance is measured at a wavelength of 560 nm and the reflectance of the standard white plate is 100%. In the white film of the present invention, by setting the relative reflectance to be 100% or more, a white film excellent in whiteness and reflection characteristics can be obtained, and particularly when used for a liquid crystal display device, a high brightness improvement effect is obtained. Can be obtained.

  Here, in order to adjust the total light transmittance and relative reflectance of the white film of the present invention within the above-mentioned ranges, 1) the dispersion diameter and density of the resin particles inside the S layer are controlled within the above-mentioned ranges. ) It can be obtained by increasing the S layer thickness. Here, in the conventional white film, in order to adjust the relative reflectance to the above-mentioned range, there was no method for increasing the film thickness of 2). In the white film of the present invention, by controlling the dispersion diameter and density of the resin particles inside the film within the above-mentioned ranges, the conventional white film cannot achieve with a thin film and has a higher hiding performance and higher reflection performance. It becomes possible to set it as a white film.

  Specifically, the white film of the present invention preferably satisfies the above-described transmittance and reflectance with a thickness of 300 μm or less. More preferably, the thickness is preferably 250 μm or less, and more preferably 225 μm or less. By satisfy | filling the transmittance | permeability and reflectance with the white film of this invention and the above-mentioned thickness, it can be set as the white film which has a highly reflective performance with a thinner film. As a result, for example, when used as a reflective member of a liquid crystal display, both a high luminance improvement effect and a thin display can be achieved.

  The specific gravity of the white film of the present invention is preferably 1.2 or less. The specific gravity here is a value determined based on JIS K7112 (1980 version). More preferably, it is 1.1 or less, More preferably, it is 1.0 or less. When the specific gravity exceeds 1.2, the occupancy ratio of the air layer is too low and the reflectance decreases, and when used as a reflector for a surface light source, the luminance tends to be insufficient, which is not preferable. In addition, the minimum of specific gravity becomes like this. Preferably it is 0.3 or more, More preferably, it is 0.4 or more. If it is less than 0.3, the mechanical strength as a film may be insufficient, or problems such as easy breakage and poor handling may occur.

  Next, although an example is demonstrated about the manufacturing method of the white film of this invention, this invention is not limited only to this example.

  A mixture containing the crystalline resin (A) chip having the above-described viscosity relationship and resin particles (incompatible resin (B)) that is incompatible with the crystalline resin (A) is required. In accordance with the above, it is sufficiently vacuum dried and supplied to a heated extruder of a film forming apparatus having an extruder (main extruder). The incompatible resin (B) may be added using a master chip prepared by uniformly melting and kneading in advance, or may be supplied directly to a kneading extruder. Further, when the resin particles are crosslinkable resin particles, it is more preferable from the viewpoint of uniform kneadability to use a material obtained by previously pulverizing components other than the incompatible resin (B).

  Further, when the white film of the present invention is a laminated film, a thermoplastic resin chip that is sufficiently vacuum-dried as necessary using a composite film forming apparatus having a sub-extruder in addition to the main extruder. Then, inorganic particles, a fluorescent brightening agent, and the like are supplied to a heated sub-extruder and coextruded and laminated.

  In addition, it is preferable to obtain a molten sheet by extrusion molding after being filtered through a filter having a mesh of 40 μm or less during melt extrusion and then introduced into a T die die.

  The molten sheet is closely cooled and solidified by static electricity on a drum cooled to a surface temperature of 10 to 60 ° C. to produce an unstretched film. The unstretched film is led to a roll group heated to a temperature of 70 to 120 ° C., stretched 3 to 4 times in the longitudinal direction (longitudinal direction, that is, the traveling direction of the film), and a roll group having a temperature of 20 to 50 ° C. Cooling.

  Subsequently, the both ends of the film are guided to a tenter while being gripped by clips, and stretched 3 to 4 times in a direction (width direction) perpendicular to the longitudinal direction in an atmosphere heated to a temperature of 90 to 150 ° C.

  The stretching ratio is 3 to 5 times in each of the longitudinal direction and the width direction, and the area ratio (longitudinal stretching ratio x lateral stretching ratio) is preferably 9 to 15 times. If the area magnification is less than 9 times, the resulting biaxially stretched laminated film has insufficient reflectivity, concealability, and film strength. Conversely, if the area magnification exceeds 15 times, the film tends to be broken during stretching. is there.

  In order to complete the crystal orientation of the obtained biaxially stretched laminated film and to give flatness and dimensional stability, heat treatment is continuously performed in a tenter at a temperature of 150 to 240 ° C. for 1 to 30 seconds, and uniform. Then, after cooling to room temperature, it is cooled to room temperature, and then, if necessary, in order to further improve the adhesion to other materials, corona discharge treatment or the like is performed and wound up, whereby the white film of the present invention can be obtained. During the heat treatment step, a relaxation treatment of 3 to 12% may be performed in the width direction or the longitudinal direction as necessary.

  In general, the higher the heat treatment temperature, the higher the thermal dimensional stability. However, the white film of the present invention is preferably heat treated at a high temperature (190 ° C. or higher) in the film forming process. This is because the white film of the present invention is desired to have a certain thermal dimensional stability. The white film of the present invention may be used as a reflective film for a surface light source (backlight) mounted on a liquid crystal display or the like. This is because the ambient temperature inside the backlight may rise to about 100 ° C. depending on the backlight.

  In particular, by setting the glass transition temperature Tg1 of the amorphous resin (B1) and / or the melting point Tm2 of the crystalline resin (B2) to the above-mentioned temperature range, even in heat treatment at high temperatures, the cyclic olefin as a void nucleating agent The copolymer is more heat-deformable (not crushed) and can maintain solid air bubbles. As a result, while maintaining high whiteness, high light reflectivity, and light weight, it can improve thermal dimensional stability. It is preferable because an excellent film can be obtained.

  In addition, the biaxial stretching method may be either sequential stretching or simultaneous biaxial stretching. However, when the simultaneous biaxial stretching method is used, it is possible to prevent film breakage in the manufacturing process or to adhere to a heating roll. Transfer defects are less likely to occur. Further, after biaxial stretching, the film may be re-stretched in either the longitudinal direction or the width direction.

  When a coating layer (C layer) is provided on the white film thus obtained, if necessary, the coating solution is applied with a micro gravure plate, kiss coat, slit die, metal ring bar, etc., and dried at 80 to 140 ° C. It can be obtained by doing later. Further, if necessary, the coating layer is cured by performing ultraviolet irradiation, heat treatment, or the like. Examples of the coating method include an in-line coating method applied during the formation of a white film, and an off-line coating method applied to the white film after the film formation, either of which can be used. The in-line coating method is preferable because it is efficient at the same time as the white film and has high adhesion to the white film, and the off-line coating method is preferable in that it is easy to form a thick coating layer. . Further, when coating, corona treatment or the like is preferably performed on the surface of the polyester film from the viewpoint of improving the wettability of the coating liquid onto the support and improving the adhesive strength. In the case of off-line coating, the coating layer (C Before forming the layer, a pretreatment such as providing an easy adhesion layer or an antistatic layer may be performed.

  To the white film of the present invention, a metal layer such as aluminum or silver may be added to the film surface by a method such as metal vapor deposition or bonding for the purpose of providing electromagnetic shielding properties or bending workability.

  The white film of the present invention is preferably used as a plate material incorporated in a surface light source for light reflection. Specifically, it is preferably used for a reflection plate of an edge light for a liquid crystal screen, a reflection plate of a surface light source of a direct type light, a reflector around a cold cathode ray tube, and the like.

In summary, in the present invention, the most preferable raw material composition of the S layer is as follows.
(1) Polyethylene terephthalate, which is a crystalline resin (A), is used as the main matrix resin.
Moreover, content of the said crystalline resin (A) in S layer is 40 to 70 weight%.
Moreover, η1 of the crystalline resin is 100 to 1000 Pa · s.
(2) Use as the resin particles a cyclic olefin copolymer that is an incompatible resin (B) with the crystalline resin and is an amorphous resin (B1). Moreover, the glass transition temperature Tg is 180 degreeC or more.
Content of the said amorphous resin (B1) in S layer is 20 to 50 weight%.
Moreover, η2 of the crystalline resin is 50 to 800 Pa · s.
(3) As a matrix, 30-40 mol% of the diol component which is the copolymer resin (C) and is an amorphous polyester resin is cyclohexanedimethanol, and 60-70 mol% of the diol component is ethylene glycol. To contain cyclohexanedimethanol copolymerized polyethylene terephthalate using terephthalic acid as the acid component.
Content of the said amorphous polyester resin in S layer is 10 to 35 weight%.
(4) A polyester-polyalkylene glycol copolymer as a dispersant (D) is contained as a matrix.
Content of the said dispersing agent (D) in S layer is 5 to 20 weight%.

(Measuring method)
A. Resin crystallinity, glass transition temperature, melting point (JIS 7121-1999, JIS 7122-1999)
According to JIS K7122 (1999) for each resin, a differential scanning calorimeter “Robot DSC-RDC220” manufactured by Seiko Denshi Kogyo Co., Ltd. was used, and a disk session “SSC / 5200” was used for data analysis. Properties, glass transition temperature, and melting point were determined. 5 mg of resin is weighed in a sample pan and heated at a heating rate of 20 ° C./min from 25 ° C. to 300 ° C. at a heating rate of 20 ° C./min 1st RUN, held in that state for 5 minutes, and then 25 ° C. In the differential scanning calorimetry chart of 2ndRUN obtained by rapidly cooling to 300 ° C. from room temperature at a rate of temperature increase of 20 ° C./min, the resin crystallinity has an exothermic peak of crystallization. What was observed (that is, the crystallization enthalpy ΔHcc obtained from the area of the crystallization exothermic peak is 1 J / g or more) is a crystalline resin, and what was not observed (that is, ΔHcc is less than 1 J / g) is amorphous Resin was used.

  In addition, the glass transition temperature is a step change in the glass transition in the 2nd RUN differential scanning calorimetry chart described above, and a step change in the glass transition and a straight line that is equidistant from the extended straight line of each base line in the vertical axis direction. It was calculated from the point where the curve of the part intersects.

  The melting point of the crystalline resin was defined as the melting point of the crystalline resin at the peak top temperature in the crystal melting peak of the differential scanning calorimetry chart of 2ndRUN.

B. Melt viscosity flow tester CFT-500 type A (manufactured by Shimadzu Corporation) was used for the measurement at a constant temperature test. That is, after preheating the resin for 5 minutes in a cylinder heated to the melting point Tm + 20 ° C. of the crystalline resin (A), a hole having a diameter of 1 mm and a length of 10 mm is formed by a piston (plunger) having a cross-sectional area of 1 cm ^2. The melt was extruded from the die having a constant load, and a melt viscosity at K factor = 1 was obtained. Furthermore, the same measurement was repeated and the average value in total 3 times was calculated. Next, after changing the weight and performing three similar measurements, the melt viscosity (unit: Pa · s) was logarithmically plotted against the shear rate (unit: sec ⁻¹ ) to obtain a power approximation curve. From the obtained approximate power curve, the melt viscosity at a shear rate of 200 sec ^-1 was extrapolated to obtain the melt viscosity.

  In addition, when resin to measure has hydrolyzability, it measured using what was dried so that a moisture content might be 50 ppm or less.

C. Resin particle diameter d, number average particle diameter Dn, volume average particle diameter Dv, number of particles per unit area, number ratio of particle diameter d of 2 μm or more Cut out the white film produced in each Example / Comparative Example, and microtome A cross section in the direction parallel to the film TD direction (transverse direction) was cut out using Pt, and platinum-palladium was vapor-deposited, followed by a 3000 to 5000 times photograph with a field emission scanning electron microscope “JSM-6700F” manufactured by JEOL Ltd. Was taken. From the obtained image, the number average particle diameter Dn was determined by the following procedures 1) to 4).

1) For each resin particle observed in the cross section of the S layer in the image, the cross-sectional area S is obtained, and the particle diameter d obtained by the following formula (1) is obtained.
d = 2 × (S / π) ^1/2 (1)
(Where π is the circumference)
2) Using the obtained particle diameter d and the number n of resin particles, Dn was calculated in the following formula (2).
Dn = Σd / n (2)
(Where Σd is the sum of the particle diameters in the observation plane, and n is the total number of particles in the observation plane)
3) Moreover, Dv was calculated | required in following formula (4).
Dv = Σ [4 / 3π × (d / 2) ³ × d] / Σ [4 / 3π × (d / 2) ³ ] (4)
(Where π is the circumference)
4) The above 1) to 3) are carried out at five places, and the average value thereof is taken as the number average particle diameter Dn and volume average particle diameter Dv of the resin particles. Note that the above evaluation is performed in an area of 2500 μm ² or more per observation point.

  5) The ratio Dv / Dn of the number average particle diameter Dv was determined from the obtained number average particle diameter Dn and volume average particle diameter Dv.

6) Further, the area of the observation region was determined, and the number of resin particles per unit area (1 μm ² ) was determined. Further, the number of particles having a particle diameter d of 2 μm or more was determined, and the ratio of the resin particles having a particle diameter d of 2 μm or more to the total number of resin particles was determined. A light reflectance of 560 nm was determined with a φ60 integrating sphere 130-0632 (Hitachi Ltd.) and a 10 ° inclined spacer attached to a relative reflectance spectrophotometer U-3410 (Hitachi Ltd.). In addition, the light reflectance was calculated | required about both surfaces of the white film, and the higher numerical value was made into the reflectance of the said white film. Part number 210-0740 manufactured by Hitachi Instrument Service Co., Ltd. was used for the standard white plate.

E. Transmittance (concealment)
The total light transmittance in the film thickness direction was measured using a haze meter NDH-5000 (manufactured by Nippon Denshoku Co., Ltd.). In addition, the transmittance | permeability calculated | required about both surfaces of the white film, and made the lower numerical value the transmittance | permeability of the said white film.

F. The specific gravity white film was cut into a size of 5 cm × 5 cm and measured using an electronic hydrometer SD-120L (Mirage Trading Co., Ltd.) based on JIS K7112 (1980 version). In addition, 5 sheets were prepared for each white film, each was measured, and the average value was used as the specific gravity of the white film.

G. The heat-resistant white film was cut into 1 cm × 15 cm strips, marked on both sides in the longitudinal direction 2.5 cm, and the width L0 was measured. Next, the sample was left in a 90 ° C. hot air oven for 30 minutes, and the distance L1 between the marks of the sample after cooling was determined. The shrinkage ratio of the sample was determined by the following formula (5).
S = (L0−L1) / L0 × 100 (5)
The measurement is performed for each of the longitudinal direction and the width direction of the film, and the respective heat shrinkage rates are obtained by the average value of each of the three samples, and the heat of the sample is obtained by the average value of the shrinkage rate in the longitudinal direction and the shrinkage rate in the width direction. The shrinkage rate was S, and the heat resistance was determined as follows.

When heat shrinkage S is 0.5% or less S
When greater than 0.5% and less than 0.8% A
When greater than 0.8% and less than 1.0% B
If greater than 1.0 C
It was.

H. A direct-type backlight with a luminance of 20 inches (16 CCFLs, fluorescent tube diameter 3 mm, fluorescent tube spacing 2.5 cm; distance between the milky white plate and fluorescent tube 1.5 cm). RM401 (manufactured by Sumitomo Chemical Co., Ltd.) as the milky white plate, light diffusion sheet “Light Up” (registered trademark) GM3 (manufactured by Kimoto Co., Ltd.), prism sheet BEFIII (manufactured by 3M), DBEF -400 (3M) was placed.

  Next, a voltage of 12 V was applied to light the CCFL, and the surface light source was activated. After 50 minutes, the central luminance was measured at a viewing angle of 1 ° and a backlight-luminance meter distance of 40 cm using a color luminance meter BM-7 / FAST (manufactured by Topcon Corporation). In each example and comparative example, three samples were measured, the average value of each was calculated, and this was designated as luminance B1.

Similarly, the reflective film was measured for a white film “Lumirror” E6SL (manufactured by Toray Industries, Inc.) having a thickness of 250 μm, and luminance B2 was obtained. Using the obtained value, the luminance improvement rate B was calculated by the following formula (6).
Brightness improvement rate B (%) = 100 × (B1−B2) / B2 (6)
I. When forming a film in the stretchable example / comparative example, S is a film that hardly causes uneven stretching, A is a film that generates slight stretch unevenness, and some stretch unevenness is slightly visible but cannot be visually recognized in the film forming process. , B, and C, which causes stretching unevenness that can be visually recognized in the film forming process. For mass production, a film forming property of B or higher is required.

  Here, stretching unevenness means that an extremely thin portion and a thick portion are generated in the stretched film. Stretch unevenness often occurs because the entire film surface is stretched non-uniformly without being stretched uniformly in the stretching step. Although various causes can be considered as the cause of stretching unevenness, in the case of the present invention, stretching unevenness tends to occur when dispersion of the incompatible resin in the polyester resin component is unstable. When stretching unevenness occurs, the reflectance and the like are often different between a thin part and a thick part, which may be undesirable.

The measurement was performed as follows by measuring the film thickness distribution in the longitudinal direction of the film. When thickness unevenness is ± 5% or less S
When greater than ± 5% and less than ± 7.5% A
When greater than ± 7.5% and less than ± 10% B
When greater than ± 10% C.

J. Film-forming properties In Examples and Comparative Examples, when film formation was little, S was the case where film breakage hardly occurred, A was slightly generated, B was slightly generated, and C was frequently generated. For mass production, a film forming property of B or higher is necessary, and if it is A or higher, there is a further cost reduction effect.

Hereinafter, the present invention will be described more specifically with reference to examples and the like, but the present invention is not limited thereto.
(material)
・ Crystalline resin (A-1)
Polyethylene terephthalate J125S (manufactured by Mitsui Chemicals, Inc.) having an intrinsic viscosity of 0.70 dl / g was used. It was 250 degreeC when melting | fusing point Tm of this resin was measured.

・ Crystalline resin (A-2)
Using terephthalic acid as the acid component and ethylene glycol as the glycol component, adding to the polyester pellets that can obtain antimony trioxide (polymerization catalyst) to 300 ppm in terms of antimony atoms, performing a polycondensation reaction, limiting viscosity Polyethylene terephthalate pellets (PET) having 0.63 dl / g and carboxyl end group amount of 40 equivalents / ton were obtained. When the heat of crystal fusion was measured using a differential thermal analyzer, it was 1 cal / g or more, and it was a crystalline polyester resin having a melting point of 250 ° C. (A-1).

・ Crystalline resin (A-3), (A-4)
The crystalline resin (A-2) is placed in a rotary vacuum device (rotary vacuum dryer) under conditions of a temperature of 220 ° C. and a vacuum degree of 0.5 mmHg, and heated with stirring for 10 and 20 hours, respectively. Polyethylene terephthalate pellets (PET) having 0.80 dl / g and carboxyl end group amount of 12 equivalents / ton were obtained, and polyethylene terephthalate pellets (PET) having an intrinsic viscosity of 1.0 dl / g and carboxyl end group amount of 10 equivalents / ton were obtained. When the heat of crystal fusion was measured using a differential thermal analyzer, respectively, it was 1 cal / g or more, and each was a crystalline polyester resin having a melting point of 250 ° C. (A-3) and (A-4).

・ Crystalline resin (A-5)
By the same method as the crystalline resin (A-2), polyethylene terephthalate pellets (PET) having an intrinsic viscosity of 0.50 dl / g and a carboxyl end group amount of 40 equivalents / ton were obtained. When the heat of crystal fusion was measured using a differential thermal analyzer, it was 1 cal / g or more, and it was a crystalline polyester resin having a melting point of 250 ° C. (A-5).

For the crystalline resins A-1 to A-5, the melt viscosity at a melting point Tm and a melting point Tm + 20 ° C. was measured. The melt viscosity was measured after vacuum drying at 180 ° C. for 3 hours. The results are shown in Table 2.

・ Incompatible resin (non-crystalline) (B1-1)
A cyclic olefin resin “TOPAS 6013” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 140 ° C. and an MVR (260 ° C./2.16 kg) of 14 ml / 10 mim was used.

・ Incompatible resin (amorphous) (B1-2)
A cyclic olefin resin “TOPAS 6015” having a glass transition temperature of 160 ° C. and an MVR (260 ° C./2.16 kg) of 4 ml / 10 mim was used.

・ Incompatible resin (non-crystalline) (B1-3)
A cyclic olefin resin “TOPAS 6017” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 180 ° C. and an MVR (260 ° C./2.16 kg) of 1.5 ml / 10 mim was used.

・ Incompatible resin (non-crystalline) (B1-4)
A cyclic olefin resin “TOPAS 6017” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 180 ° C. and an MVR (260 ° C./2.16 kg) of 4.5 ml / 10 mim was used.

・ Incompatible resin (non-crystalline) (B1-5)
A cyclic olefin resin “TOPAS 6018” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and an MVR (260 ° C./2.16 kg) of 1.5 ml / 10 mim was used.

・ Incompatible resin (non-crystalline) (B1-6)
A cyclic olefin resin “TOPAS 6018X1 T4 Sack No. 32” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and MVR (260 ° C./2.16 kg) of 2.0 ml / 10 mim was used.

・ Incompatible resin (non-crystalline) (B1-7)
A cyclic olefin resin “TOPAS 6018X1 T2 Lot No 060286” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and an MVR (260 ° C./2.16 kg) of 3.0 ml / 10 mim was used.

・ Incompatible resin (non-crystalline) (B1-8)
A cyclic olefin resin “TOPAS 6018 TOPAS 6018X1 T5” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and an MVR (260 ° C./2.16 kg) of 4.5 ml / 10 mim was used.

・ Incompatible resin (amorphous) (B1-9)
A cyclic olefin resin “TOPAS 6018X1 T6 Sack No. 1” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and MVR (260 ° C./2.16 kg) of 7.0 ml / 10 mim was used.

・ Incompatible resin (amorphous) (B1-10)
Cyclic olefin resin “TOPAS 6018X1 T6 Sack No. 205” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and MVR (260 ° C./2.16 kg) of 10.0 ml / 10 mim was used.

・ Incompatible resin (non-crystalline) (B1-11)
A cyclic olefin resin “TOPAS 6018X1 T6 Sack No. 220 (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and an MVR (260 ° C./2.16 kg) of 20.0 ml / 10 mim was used.

・ Incompatible resin (amorphous) (B1-12)
A cyclic olefin resin “TOPAS 6018X1 T7” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and an MVR (260 ° C./2.16 kg) of 15.0 ml / 10 mim was used.

・ Incompatible resin (amorphous) (B1-13)
A cyclic olefin resin “TOPAS 6018X1 T6 Sack No. 245” (manufactured by Nippon Polyplastics Co., Ltd.) having a glass transition temperature of 190 ° C. and an MVR (260 ° C./2.16 kg) of 80.0 ml / 10 mim was used.

  In addition, the resin of the incompatible resin (amorphous) B1-1 to 12 ("TOPAS 6013", "TOPAS 6015", "TOPAS 6017", "TOPAS 6018") is composed of a norbornene component and an ethylene component as shown in Chemical Formula 1. Composed.

  The composition of each component is shown in Table 1. In addition, when any resin measured the heat of crystal fusion using the differential thermal analyzer, it was less than 1 cal / g and was an amorphous resin.

・ Incompatible resin (crystalline) (B2-1)
An acyclic polyolefin-based resin PMP (polymethylpentene) “TPX DX845” (manufactured by Mitsui Chemicals, Inc.) having a melt fluoride (260 ° C./5.0 kg) of 8 g / 10 mim was used. When the heat of crystal fusion was measured using a differential thermal analyzer, it was 1 cal / g or more, which was a crystalline resin. The glass transition temperature was 25 ° C. and the melting point was 235 ° C.

・ Incompatible resin (crystalline) (B2-2)
An acyclic polyolefin-based resin PMP (polymethylpentene) “TPX DX820” (manufactured by Mitsui Chemicals, Inc.) having a melt fluoride (260 ° C./5.0 kg) of 180 g / 10 mim was used. When the heat of crystal fusion was measured using a differential thermal analyzer, it was 1 cal / g or more, which was a crystalline resin. The glass transition temperature was 25 ° C. and the melting point was 235 ° C.

・ Incompatible resin (crystalline) (B2-3)
An acyclic polyolefin-based resin PMP (polymethylpentene) (manufactured by Mitsui Chemicals, Inc.) having a melt fluoride (260 ° C./5.0 kg) of 100 g / 10 mim was used. When the heat of crystal fusion was measured using a differential thermal analyzer, it was 1 cal / g or more, which was a crystalline resin. The glass transition temperature was 25 ° C. and the melting point was 235 ° C.

  Regarding the incompatible resins B1-1 to 10 and B2-1 to B3-1, the melt viscosity η2 of the crystalline resin A at the melting point Tg + 20 ° C. was measured. The results are shown in Table 3.

・ Copolymerized polyester (C)
CHDM (cyclohexanedimethanol) copolymerized PET “PETG 6763” (manufactured by Eastman Chemical) was used. It is PET obtained by copolymerizing 33 mol% of cyclohexanedimethanol with the copolymerized glycol component. When the heat of crystal fusion was measured using a differential thermal analyzer, it was less than 1 cal / g, which is an amorphous polyester resin (C).

・ Dispersant (D)
A PBT-PAG (polyalkylene glycol) copolymer “Hytrel 7247” (manufactured by Toray DuPont Co., Ltd.) was used. The resin is a block copolymer of PBT (polybutylene terephthalate) and PAG (mainly polytetramethylene glycol). When the heat of crystal fusion was measured using a differential thermal analyzer, it was 1 cal / g or more, which was a crystalline resin.

(Examples 1-1, 1-2, 1-12, 1-16, 1-18, 1-19, 1-25)
The raw material mixture shown in Table 5 was vacuum-dried at a temperature of 180 ° C. for 3 hours, then supplied to an extruder, melt-extruded at a temperature of 280 ° C., filtered through a 30 μm cut filter, and then introduced into a T die die. .

  Next, the molten single layer sheet is extruded from the inside of the T die die into a molten single layer sheet, and the molten single layer sheet is closely cooled and solidified by an electrostatic application method on a drum maintained at a surface temperature of 25 ° C. A layer film was obtained. Subsequently, the unstretched single layer film was preheated with a roll group heated to a temperature of 85 ° C., and then stretched 3.3 times in the longitudinal direction (longitudinal direction) using a heating roll having a temperature of 90 ° C. A uniaxially stretched film was obtained by cooling with a roll group at a temperature of ° C.

While holding both ends of the obtained uniaxially stretched film with clips, it is guided to a preheating zone at a temperature of 95 ° C. in the tenter, and continuously in a heating zone at a temperature of 105 ° C. in a direction perpendicular to the longitudinal direction (width direction). 3.2 Stretched 2 times. Subsequently, a heat treatment is performed for 20 seconds at a predetermined temperature (see Table 5) in a heat treatment zone in the tenter, and further, a relaxation treatment is performed in a 4% width direction at a temperature of 180 ° C., and then at a temperature of 140 ° C. A relaxation treatment was performed in the 1% width direction. Subsequently, the film was gradually cooled and wound up to obtain a single-layer white film having a thickness of 188 μm. The stretchability and film forming property were both good, and the film forming property was particularly better when the crystalline resin (A-1) was used. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. As described above, the white film of the present invention exhibits excellent whiteness, reflectivity, and lightness, and has good thermal dimensional stability, particularly when the crystalline resin (A-2) is used. Met. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that high luminance was exhibited.

(Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (Comparative Example) , 1-21)
A white film was obtained in the same manner as in Example 1-1 except that the mixture of raw materials shown in Table 5 was used and the heat treatment temperature was changed to the temperature shown in Table 4. The stretchability and film forming property were both good, and the film forming property was particularly better when the crystalline resin (A-1) was used. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. Although these white films do not reach Example 1-1, they exhibit excellent properties such as whiteness, reflectivity, and lightness, and all have good thermal dimensional stability. In particular, the crystalline resin (A- The thermal dimensional stability was better when 2) was used. Moreover, when the obtained white film was incorporated into a backlight and evaluated for luminance, it was found that the luminance was high although it did not reach Example 1-1.

( Comparative Examples 1-8, 1-10)
A white film was obtained in the same manner as in Example 1-1 except that the mixture of raw materials shown in Table 5 was used and the heat treatment temperature was changed to the temperature shown in Table 5. Although the stretchability was slightly inferior to that of Example 1-1, the film forming property was good. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. These white films exhibited excellent whiteness, reflectivity, and lightness. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that high luminance was exhibited. However, the thermal dimensional stability was slightly inferior to that of Example 1-1.

( Comparative Examples 1-9, 1-11)
A white film was obtained in the same manner as in Example 1-1 except that the mixture of raw materials shown in Table 5 was used and the heat treatment temperature was changed to the temperature shown in Table 5. Although the stretchability was slightly inferior to that of Example 1-1, the film forming property was good. When the cross section of the white film was observed, it contained a large number of fine bubbles with resin particles as the core, but the resin particles were slightly flattened. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. These white films are inferior to Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (Comparative Examples) and 1-21, but are white, reflective and lightweight. The thermal dimensional stability was good. Moreover, when the brightness | luminance evaluation was carried out by incorporating the obtained white film in a backlight, Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (comparative example) , 1- Although it was inferior to 21, it turned out that a high luminance is shown.

( Comparative Example 1-5, Examples 1-6, 1-14, 1-15, Comparative Example 1-22)
A white film was obtained in the same manner as in Example 1-1 except that the mixture of raw materials shown in Table 5 was used. The stretchability and film forming property were both good, and the film forming property was particularly better when the crystalline resin (A-1) was used. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. Although these white films are less than Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (Comparative Example) , 1-21, whiteness, reflectivity, The characteristics excellent in lightness were exhibited, the thermal dimensional stability was good, and the thermal dimensional stability was particularly good when the crystalline resin (A-2) was used. Moreover, when the brightness | luminance evaluation was carried out by incorporating the obtained white film in a backlight, Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (comparative example), 1- Although it was less than 21, it was found to show high luminance.

(Examples 1-23 and 1-24)
A white film was obtained in the same manner as in Example 1-1 except that the film thickness shown in Table 5 was used. The stretchability and film forming property were both good. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. As described above, the white film of the present invention exhibited excellent whiteness, reflectivity, and lightness, and the thermal dimensional stability was good. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that the luminance was higher than that of Example 1-1.

(Example 1-26)
A white film was obtained in the same manner as in Example 1-1 except that the mixture of raw materials shown in Table 5 was used. The stretchability and film forming property were good. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. These white films exhibited excellent whiteness, reflectivity, and lightness. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that the luminance was high, although not as high as that of Example 1-1. However, the thermal dimensional stability was slightly inferior to that of Example 1-1.

( Comparative Example 1-27)
A white film was obtained in the same manner as in Example 1-1 except that the mixture of raw materials shown in Table 5 was used. The stretchability and film forming property were good. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. Although these white films are less than Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (Comparative Example) , 1-21, whiteness, reflectivity, The characteristic which was excellent in lightness was shown. Moreover, when the brightness | luminance evaluation was carried out by incorporating the obtained white film in a backlight, Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (comparative example) , 1- Although it was less than 21, it was found to show high luminance. However, the thermal dimensional stability was slightly inferior to that of Example 1-1.

( Comparative Example 1-28)
A white film was obtained in the same manner as in Example 1-1 except that the mixture of raw materials shown in Table 5 was used. The drawability was good, but tearing occurred frequently during film formation, and the film formation was lower than in other examples. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. Although these white films are less than Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (Comparative Example) , 1-21, whiteness, reflectivity, The characteristic which was excellent in the lightness was shown, and all the thermal dimensional stability was favorable. Moreover, when the brightness | luminance evaluation was carried out by incorporating the obtained white film in a backlight, Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (comparative example) , 1- Although it was less than 21, it was found to show high luminance.

( Comparative Examples 2-1 and 2-2)
A white film was obtained in the same manner as in Example 1-1 except that the mixture of raw materials shown in Table 5 was used and the heat treatment temperature was changed to the temperature shown in Table 5. The stretchability was good, and the film-forming property was good although it was inferior to Example 1-1 to Example 1-25. When the cross section of this white film was observed, it contained a large number of fine bubbles centered on the resin particles, but the resin particles were slightly flattened. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. These white films are inferior to Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (Comparative Examples) and 1-21, but are white, reflective and lightweight. Excellent thermal dimensional stability. Moreover, when the brightness | luminance evaluation was carried out by incorporating the obtained white film in a backlight, Examples 1-3, 1-4, 1-7, 1-13, 1-17, 1-20 (comparative example) , 1- Although it was inferior to 21, it turned out that a high luminance is shown.

( Comparative Examples 2-3, 2-4)
A white film was obtained in the same manner as in Example 1-1 except that the film thickness shown in Table 5 was used. The stretchability was good, and the film-forming property was good although it was inferior to Example 1-1 to Example 1-25. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. These white films exhibited excellent properties such as whiteness, reflectivity, lightness, and thermal dimensional stability. Moreover, when the obtained white film was incorporated into a backlight and evaluated for luminance, it was found that the luminance was higher than Comparative Examples 2-1 and 2-2.

(Examples 3-1 and 3-7)
In a composite film-forming apparatus having a main extruder and a sub-extruder, the raw material mixture for the main layer (A layer) shown in Table 6 is vacuum dried at 170 ° C. for 5 hours, and then supplied to the main extruder side. After melt extrusion at a temperature of 280 ° C., the mixture was filtered through a 30 μm cut filter and then introduced into a T-die composite die.

  On the other hand, the sub-extruder is dried in a vacuum at a temperature of 170 ° C. for 5 hours after mixing the raw material for the sub-layer (B) layer shown in Table 6 and then supplied to the sub-extruder and after melt extrusion at a temperature of 280 ° C. After filtration through a 30 μm cut filter, it was introduced into a T-die composite die.

  Next, in the T-die composite die, the resin layer (B) extruded from the sub-extruder is laminated (B / A / B) on both surface layers of the resin layer (A) extruded from the main extruder. After merging, the sheet was coextruded into a molten laminated sheet, and the molten laminated sheet was closely cooled and solidified by an electrostatic charge method on a drum maintained at a surface temperature of 25 ° C. to obtain an unstretched laminated film. Subsequently, the unstretched laminated film is preheated with a group of rolls heated to a temperature of 85 ° C. according to a conventional method, and then stretched 3.3 times in the longitudinal direction (longitudinal direction) using a heating roll having a temperature of 90 ° C. And cooled with a roll group at a temperature of 25 ° C. to obtain a uniaxially stretched film.

While holding both ends of the obtained uniaxially stretched film with clips, it is guided to a preheating zone at a temperature of 95 ° C. in the tenter, and continuously in a heating zone at a temperature of 105 ° C. in a direction perpendicular to the longitudinal direction (width direction). 3.2 Stretched 2 times. Subsequently, heat treatment was performed for 20 seconds at a predetermined temperature (see table) in the heat treatment zone in the tenter, and further relaxation treatment was performed in the 4% width direction at a temperature of 180 ° C. The relaxation treatment was performed in the% width direction. Next, after gradually cooling uniformly, it is wound up so that the ratio of the thickness of the A layer and the B layer is B layer / A layer / B layer = 1/20/1, and a laminated white film having a total thickness of 188 μm is obtained. Obtained. When the cross-sectional structure of the obtained film was confirmed, it was confirmed that the A layer contained a large number of fine bubbles having resin particles as nuclei. In addition, Table 6 shows the number average particle diameter Dn of the resin particles in the A layer, the number of resin particles (number / μm ² ), the ratio having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 6 shows various characteristics of the film. These white films exhibit excellent properties such as whiteness, reflectivity, and lightness, have good thermal dimensional stability, and are manufactured as compared with single film (Examples 1-1 and 1-18). It was found that the film was excellent. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that high luminance was exhibited as in Examples 1-1 and 1-18.

(Examples 3-2 and 3-8)
The thicknesses of the A and B layers were the same as in Examples 3-1 and 3-7, except that PET containing 5% by weight of titanium oxide having a number average particle size of 0.5 μm was used as the raw material for the B layer. A laminated white film having a thickness ratio of B layer / A layer / B layer = 1/20/1 and a total thickness of 188 μm was obtained. In addition, Table 6 shows the number average particle diameter Dn of the resin particles in the A layer, the number of resin particles (number / μm ² ), the ratio having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. When the cross-sectional structure of the obtained film was confirmed, it was confirmed that the A layer contained a large number of fine bubbles having resin particles as nuclei. Table 6 shows various characteristics of the film. These white films have excellent whiteness, reflectivity, and lightness, have good thermal dimensional stability, and are concealed compared to single film (Examples 1-1 and 1-18). The film was found to have excellent properties and film forming properties. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that the luminance was higher than that of Examples 1-1 and 1-18.

(Examples 3-3, 3-4, 3-9, 3-10)
As shown in Table 6, PET containing 10% by weight of calcium carbonate having a number average particle size of 0.5 μm and PET containing 10% by weight of barium sulfate having a number average particle size of 0.5 μm are used as the raw material for the B layer. In the same manner as in Examples 3-1 and 3-7, except that the ratio of the thickness of the A layer and the B layer was B layer / A layer / B layer = 1/20/1, and the total thickness was 188 μm. A film was obtained. In addition, Table 6 shows the number average particle diameter Dn of the resin particles in the A layer, the number of resin particles (number / μm ² ), the ratio having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. When the cross-sectional structure of the obtained film was confirmed, it was confirmed that the A layer contained a large number of fine bubbles having resin particles as nuclei. Table 6 shows various characteristics of the film. These white films exhibit excellent properties such as whiteness, reflectivity, and lightness, have good thermal dimensional stability, and are more reflective than single film (Examples 1-1 and 1-18). It turned out that it was excellent in the characteristic and film forming property. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that the luminance was higher than those of Examples 1-1 and 1-18.

(Examples 3-5, 3-6, 3-11, 12)
A laminated white film was obtained in the same manner as in Examples 3-1 and 3-7 except that the film thickness was as shown in Table 6. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 6 shows various characteristics of the film. These white films exhibited characteristics excellent in whiteness, reflectivity, and lightness as compared with Examples 3-1 and 3-7, and the thermal dimensional stability was good. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that the luminance was higher than those of Examples 3-1 and 3-7.

(Example 4-1)
Except for using the raw materials shown in Table 6, the ratio of the thickness of the A layer to the B layer was B layer / A layer / B layer = 1/20 in the same manner as in Examples 3-1 and 3-7. / 1, a laminated white film having a total thickness of 188 μm was obtained. In addition, Table 6 shows the number average particle diameter Dn of the resin particles in the A layer, the number of resin particles (number / μm ² ), the ratio having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. When the cross-sectional structure of the obtained film was confirmed, it was confirmed that the A layer contained a large number of fine bubbles having resin particles as nuclei. Although this white film was inferior to Examples 3-1 and 3-7, it showed excellent whiteness, reflectivity, and lightness, and its thermal dimensional stability was superior to that of Example 3-1. It was found that the film-forming property was excellent as compared with a single film (Example 2-1). Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that Examples 3-1 and 3-7 showed high luminance although inferior.

(Example 4-2)
The ratio of the thickness of the A layer to the B layer is the same as in Example 4-1, except that PET containing 5% by weight of titanium oxide having a particle size of 0.5 μm is used as the raw material for the B layer. A laminated white film having / A layer / B layer = 1/20/1 and a total thickness of 188 μm was obtained. In addition, Table 6 shows the number average particle diameter Dn of the resin particles in the A layer, the number of resin particles (number / μm ² ), the ratio having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. When the cross-sectional structure of the obtained film was confirmed, it was confirmed that the A layer contained a large number of fine bubbles having resin particles as nuclei. Table 6 shows various characteristics of the film. This white film showed characteristics excellent in whiteness, reflectivity, lightness, and thermal dimensional stability, and was found to be excellent in hiding properties as compared with a single film (Example 2-1). . Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that the luminance was high although it was inferior to that of Example 4-1.

(Examples 4-3 and 4-4)
As shown in Table 6, PET containing 10% by weight of calcium carbonate having a number average particle size of 0.5 μm and PET containing 10% by weight of barium sulfate having a number average particle size of 0.5 μm are used as the raw material for the B layer. A laminated white film was obtained in the same manner as in Example 4-1, except that the ratio of the thickness of the A layer and the B layer was B layer / A layer / B layer = 1/20/1 and the total thickness was 188 μm. . In addition, Table 6 shows the number average particle diameter Dn of the resin particles in the A layer, the number of resin particles (number / μm ² ), the ratio having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. When the cross-sectional structure of the obtained film was confirmed, it was confirmed that the A layer contained a large number of fine bubbles having resin particles as nuclei. Table 6 shows various characteristics of the film. These white films exhibited characteristics excellent in whiteness, reflectivity, and lightness as compared with Example 4-1, and were excellent in thermal dimensional stability. Moreover, when the obtained white film was incorporated in a backlight and evaluated for luminance, it was found that the luminance was higher than that of Example 4-1.

(Examples 4-5 and 6)
A laminated white film was obtained in the same manner as in Example 4-1, except that the film thickness shown in Table 6 was used. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. Table 5 shows the number average particle diameter Dn of the resin particles in the film, the number of resin particles (number / μm ² ), the proportion having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Table 5 shows various characteristics of the film. These white films exhibited characteristics excellent in whiteness, reflectivity, and lightness as compared with Example 4-1, and were excellent in thermal dimensional stability. Moreover, when the obtained white film was incorporated into a backlight and evaluated for luminance, it was found that the luminance was higher than that of Example 4-1.

(Comparative Examples 1-1 to 6, 2-1 to 2-4)
Using the raw materials shown in Table 5, a film was formed in the same manner as in Example 1-1 except that the heat treatment temperature shown in Table 5 was used, to obtain a single film having a thickness of 188 μm. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. However, the results of the number average particle diameter Dn of resin particles, the number of resin particles (number / μm ² ), the ratio of having a particle diameter of 2 μm or more, and the volume average particle diameter Dv are shown in Table 5, but inferior to those of the examples. I understood that. Moreover, although the various characteristics of a film are shown in Table 5, it is inferior in concealability and reflectivity, and when the brightness | luminance evaluation was carried out incorporating the obtained white film in a backlight, compared with Example 1-1, a brightness | luminance is significantly inferior. I understood that.

(Comparative Example 5-1)
65 parts by weight of polyethylene terephthalate pellets (PET) having an intrinsic viscosity of 0.63 dl / g and a carboxyl end group amount of 40 equivalents / ton, and 20 parts by weight of a number average particle diameter of 0 A film was formed in the same manner as in Example 1-1 except that a chip prepared by mixing 15% by weight of 8 μm barium sulfate with a biaxial kneader was used. Although a single film having a thickness of 188 μm could be obtained, the film was frequently broken during film formation, and the film-forming property was poor as compared with Example 1-1. When the cross section of this white film was observed, it contained many fine bubbles with inorganic particles as the core. Table 7 shows the results of the number average particle diameter Dn of the inorganic particles in the film, the number of inorganic particles (number / μm ² ), the ratio having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Moreover, although the various characteristics of a film are shown in Table 7, when it was inferior in reflectivity and the brightness | luminance evaluation was carried out by incorporating the obtained white film in a backlight, it turned out that a brightness | luminance is significantly inferior compared with Example 1-1. It was.

(Comparative Example 5-2)
20 parts by weight of a polyethylene terephthalate pellet (PET) having an intrinsic viscosity of 0.63 dl / g and a carboxyl end group amount of 40 equivalents / ton, and 20 parts by weight of a number average particle diameter of 0 The film was formed in the same manner as in Example 1-1 except that a chip prepared by mixing 20% by weight of barium sulfate of 8 μm with a twin-screw kneader was used, but the film was broken frequently and a white film was obtained. I couldn't.

(Comparative Examples 3-1 to 3-4, 3-5 to 3-8, 4-1 to 4-4)
Using the raw materials shown in Tables 6 and 7, a film was formed in the same manner as in Examples 3-1 to 3-4, respectively, to obtain a single film having a thickness of 188 μm. When the cross section of this white film was observed, it contained many fine bubbles with resin particles as the core. However, the results of the number average particle diameter Dn of the resin particles, the number of resin particles (number / μm ² ), the ratio of having a particle diameter of 2 μm or more, and the volume average particle diameter Dv are shown in Table 5; It turned out to be inferior compared to ~ 3-4. Moreover, although the various characteristics of a film are shown in Table 6, it is inferior in concealability and reflectivity, and when the brightness | luminance evaluation was carried out incorporating the obtained white film in a backlight, compared with Examples 3-1 to 3-4, respectively. The brightness was found to be significantly inferior.

(Comparative Examples 5-3 to 5-6)
Using the raw materials shown in Table 7, film formation was performed in the same manner as in Examples 3-1 to 3-4. Although a single film having a thickness of 188 μm could be obtained, the film was frequently broken during film formation, and the film-forming property was poor as compared with Examples 3-1 to 3-4. When the cross section of this white film was observed, it contained many fine bubbles with inorganic particles as the core. Table 7 shows the results of the number average particle diameter Dn of the inorganic particles in the film, the number of inorganic particles (number / μm ² ), the ratio having a particle diameter of 2 μm or more, and the volume average particle diameter Dv. Moreover, although the various characteristics of a film are shown in Table 7, when it is inferior in reflectivity and the brightness | luminance evaluation was carried out incorporating the obtained white film in a backlight, compared with Examples 3-1 to 3-4, brightness | luminance was large. I found it inferior. In the above description and table, 1-5, 1-8 to 1-11, 1-20, 1-22, 1-27, 1-28, 2-1 to 2-4 are comparative examples. It is.

  The white film of the present invention is excellent in reflection characteristics, lightness, and the like, particularly when used as a reflector or reflector in a surface light source, can brightly illuminate the liquid crystal screen, making the liquid crystal image clearer and easier to see, It is useful.

Claims (7)

The matrix containing at least the crystalline resin (A) contains the resin (B) that is incompatible with the crystalline resin (A) (hereinafter referred to as incompatible resin (B)) as resin particles, and there are bubbles inside. In the white film having the layer having S (S layer), the incompatible resin (B) is an amorphous resin (B1), and the glass transition temperature Tg1 of the incompatible resin (B1) is 170 ° C. or higher. The melt viscosity η1 of the crystalline resin (A) at a melting point Tm + 20 ° C. and a shear rate of 200 sec ⁻¹ of the crystalline resin (A) is 10% by weight or more based on the total material constituting the S layer. A white film in which the melt viscosity η2 (Pa · s) of (Pa · s) and the incompatible resin (B) satisfies the following (1) and (2).
(1) −0.1 ≦ log ₁₀ (η2 / η1) ≦ 0.45
(2) 0.95 ≦ log ₁₀ (η2) / log ₁₀ (η1) ≦ 1.20
The white film according to claim 1, wherein a difference η2-η1 between the melt viscosity η1 of the crystalline resin (A) and the melt viscosity η2 of the incompatible resin (B) is -300 to 1000 Pa · s. The white film according to claim 2, wherein the incompatible resin (B1) is a cyclic olefin copolymer. The white film according to any one of claims 1 to 3 , wherein the crystalline resin (A) is a polyester resin. White film according to any one of claims 1-4 relative reflectance of 100% or more. The white film in any one of Claims 1-5 used for the reflective film for surface light sources. A surface light source using the white film according to claim 6 .