JP2005190529A - Polyester film for process paper of high density dvd light transmission protection layer - Google Patents

Polyester film for process paper of high density dvd light transmission protection layer Download PDF

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JP2005190529A
JP2005190529A JP2003428933A JP2003428933A JP2005190529A JP 2005190529 A JP2005190529 A JP 2005190529A JP 2003428933 A JP2003428933 A JP 2003428933A JP 2003428933 A JP2003428933 A JP 2003428933A JP 2005190529 A JP2005190529 A JP 2005190529A
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layer
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polyester film
light transmission
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JP4251981B2 (en
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Shigeo Uchiumi
滋夫 内海
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Mitsubishi Polyester Film Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a polyester film being excellent in running and smoothing, and being suitable for a process paper used when a high density DVD light transmission protection layer is prepared. <P>SOLUTION: This film is the laminating polyester film used for the process paper of the high density DVD light transmission protection layer, and average roughness of a center plane (SRa(A)) of one film plane (A plane) is 20 nm or less, and average roughness of a center plane (SRa(C)) of the other film plane (C plane) is larger than SRa(A). <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

本発明は、DVDの高密度化のために必要な薄膜化された光透過保護層の作成の際に用いられる工程紙に使用されるベースフィルムに関する。   The present invention relates to a base film used for process paper used in the production of a thinned light-transmitting protective layer necessary for increasing the density of a DVD.

コンピューター用、オーディオ用等の各種情報を記録する高密度記録媒体として、再生記録を光照射にて行う光ディスク、その中でもDVDは、新三種の神器の一つとして注目されているが、近年地上波デジタル放送やハイビジョン放送に対応するために、その大容量化がますます要求されている。   As a high-density recording medium for recording various types of information for computers, audio, etc., optical discs that perform reproduction and recording by light irradiation, and DVD among them, are attracting attention as one of the three new treasures. In order to cope with digital broadcasting and high-definition broadcasting, there is an increasing demand for larger capacity.

従来のDVDでは、厚み600μmの基板を2枚貼り合わせる構造が取られていたが、大容量化の一つの手段として、レーザー光の通過する光透過層が薄いほど有利なために、厚さ約100μmの光学フィルムを、接着剤を介して基板と貼り合わせ、フィルム側から信号を読みとる構造のディスクが開発中である。   The conventional DVD has a structure in which two substrates having a thickness of 600 μm are bonded together. However, as one means for increasing the capacity, the thinner the light transmission layer through which laser light passes, the more advantageous the thickness is. A disc having a structure in which a 100 μm optical film is bonded to a substrate via an adhesive and a signal is read from the film side is under development.

大容量化のためのもう一つの重要な技術は、光ピックアップ部に用いるレーザー光の短波長化がある。現在DVDには、波長が約650nmの赤色のレーザー光が用いられているが、波長が405nmの青色レーザーの適用も開発中である。しかし、波長が短くなればなるほど、記録媒体表面の細かい厚み変動による影響を受けやすくなり、信号特性を評価したときにノイズが発生しやすくなるため、特に表面平滑性が必要とされるのである。   Another important technique for increasing the capacity is to shorten the wavelength of laser light used in the optical pickup section. Currently, red laser light having a wavelength of about 650 nm is used for DVD, but application of a blue laser having a wavelength of 405 nm is also under development. However, the shorter the wavelength, the more easily affected by fine thickness variations on the surface of the recording medium, and noise is more likely to occur when signal characteristics are evaluated, so surface smoothness is particularly required.

基板は主に射出成形によって作られているが、射出成形で薄膜を成形する場合には、成型時の冷却ムラ等により光学ムラが出やすくなるため、300μm以下のシートやフィルムを作るには適していない。そのため、樹脂を溶液に溶解させて、塗工・乾燥を行う溶液キャスト法での製膜が光学フィルム(光透過保護層)の製造方法に用いられつつある。溶液法では、光学均一性の面で優れると共に粘度が低いために濾過等により異物の除去が容易なためである。   The substrate is mainly made by injection molding. However, when forming a thin film by injection molding, optical unevenness is likely to occur due to cooling unevenness during molding, so it is suitable for making sheets and films of 300 μm or less. Not. Therefore, film formation by a solution casting method in which a resin is dissolved in a solution and coating and drying are being used in a method for manufacturing an optical film (light transmission protective layer). This is because the solution method is excellent in terms of optical uniformity and has a low viscosity, so that foreign matters can be easily removed by filtration or the like.

この溶液キャスト法で光学フィルムの製膜を行う場合には、支持体として金属のエンドレスベルトやドラムを用いる場合と、プラスチックや金属のフィルムもしくはシートを用いる場合が一般的であったが、搬送性、柔軟性に優れ、エンドレスベルトなどに特有の継ぎ目の段差がないことから、プラスチックフィルムを支持体として用いる方法が特に好まれている。さらにフィルムの剛性が高く、耐薬品性が良好かつ安価な点でPET(ポリエチレンテレフタレート)フィルムが好ましく用いられてきた。さらにPETフィルムの表面を平滑にするためにフィルムの片面をハードコートしたものも用いられてきた。しかしながら、ハードコート面の平滑性を重視する余り、表面の平滑なベースフィルムが使用されたが、フィルムの走行性が悪く、部分的に信号のエラーがあり、実用的でない状況である(特許文献1,2)。
特開2003−326542号公報 特開2003−326543号公報 特開2002−238706号公報
In the case of forming an optical film by this solution casting method, a case where a metal endless belt or drum is used as a support and a case where a plastic or metal film or sheet is used are generally used. The method using a plastic film as a support is particularly preferred because it has excellent flexibility and has no joint step characteristic of an endless belt. Furthermore, a PET (polyethylene terephthalate) film has been preferably used because of its high rigidity, good chemical resistance and low cost. Furthermore, in order to smooth the surface of the PET film, a film having one surface hard-coated has been used. However, a base film with a smooth surface was used because the smoothness of the hard coat surface was emphasized. However, the running property of the film was poor, there was a signal error in part, and the situation was not practical (Patent Literature). 1, 2).
JP 2003-326542 A JP 2003-326543 A JP 2002-238706 A

本発明は、このような問題点を解決しようとするものであり、その解決課題は、走行性と平滑性に優れ、高密度化DVDの光透過保護層の作成の際に用いられる工程紙として好適なポリエステルフィルムを提供することにある。   The present invention is intended to solve such problems, and the problem to be solved is as a process paper that is excellent in runnability and smoothness, and used in the production of a light-transmitting protective layer for high-density DVDs. The object is to provide a suitable polyester film.

本発明者らは、上記課題を解決するために鋭意検討した結果、特定の構成を有するフィルムにより、上記課題が容易に解決できることを見いだし、本発明を完成するに至った。   As a result of intensive studies to solve the above problems, the present inventors have found that the above problems can be easily solved by a film having a specific configuration, and have completed the present invention.

すなわち、本発明の要旨は、高密度DVD光透過保護層の工程紙として使用されるポリエステルフィルムであって、一方のフィルム面(A面)の中心面平均粗さ(SRa(A))が20nm以下であり、もう一方のフィルム面(C面)の中心面平均粗さ(SRa(C))がSRa(A)よりも大きいことを特徴とする積層ポリエステルフィルムに存する。   That is, the gist of the present invention is a polyester film used as a process paper for a high-density DVD light transmission protective layer, and the average roughness (SRa (A)) of one film surface (A surface) is 20 nm. The present invention resides in a laminated polyester film characterized in that the center plane average roughness (SRa (C)) of the other film surface (C surface) is larger than SRa (A).

以下、本発明を詳細に説明する。
本発明でいうポリエステルとは、ジカルボン酸とジオールとから、あるいはジカルボン酸とヒドロキシカルボン酸とから重縮合によって得られるエステル基を含むポリマーを指す。ジカルボン酸としては、テレフタル酸、コハク酸、イソフタル酸、アジピン酸、アゼライン酸、セバシン酸、ドデカン二酸、2,6−ナフタレンジカルボン酸、1,4−シクロヘキサンジカルボン酸等を、ジオールとしては、エチレングリコール、1,3−プロパンジオール、1,6−ヘキサンジオール、1,4−ブタンジオール、ジエチレングリコール、トリエチレングリコール、ネオペンチルグリコール、1,4−シクロヘキサンジメタノール、ポリエチレングリコール等を、ヒドロキシカルボン酸としては、p−ヒドロキシ安息香酸、6−ヒドロキシ−2−ナフトエ酸等をそれぞれ例示することができる。
Hereinafter, the present invention will be described in detail.
The polyester referred to in the present invention refers to a polymer containing an ester group obtained by polycondensation from dicarboxylic acid and diol or from dicarboxylic acid and hydroxycarboxylic acid. Examples of the dicarboxylic acid include terephthalic acid, succinic acid, isophthalic acid, adipic acid, azelaic acid, sebacic acid, dodecanedioic acid, 2,6-naphthalenedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, and the diol includes ethylene. Glycol, 1,3-propanediol, 1,6-hexanediol, 1,4-butanediol, diethylene glycol, triethylene glycol, neopentyl glycol, 1,4-cyclohexanedimethanol, polyethylene glycol, etc. as hydroxycarboxylic acids Can be exemplified by p-hydroxybenzoic acid, 6-hydroxy-2-naphthoic acid and the like.

かかるポリマーの代表的なものとして、ポリエチレンテレフタレートやポリブチレンテレフタレート、ポリエチレン−2,6―ナフタレート等が例示される。これらのポリマーはホモポリマーであってもよく、また第3成分を共重合させたものでもよい。   Typical examples of such polymers include polyethylene terephthalate, polybutylene terephthalate, and polyethylene-2,6-naphthalate. These polymers may be homopolymers or may be a copolymer of the third component.

本発明のフィルムとしては、優れた強度や寸法安定性の観点から二軸延伸フィルムが好ましく用いられるが、未延伸または少なくとも一方に延伸されたポリエステルフィルムを用いることもできる。   As the film of the present invention, a biaxially stretched film is preferably used from the viewpoint of excellent strength and dimensional stability, but a polyester film that has not been stretched or stretched at least in one direction can also be used.

本発明におけるポリエステルフィルムは、一方の表面(A面)のSRa(A)が20nm以下、好ましくは10nm以下、さらに好ましくは5nm以下である。A面は、キャストフィルム設置面となる面であり、A面のSRa(A)が20nmより大きい場合、キャストフィルムを設置した際に、キャストフィルムの支持体と接する面の平滑性が不十分となり好ましくない。   In the polyester film of the present invention, SRa (A) on one surface (A surface) is 20 nm or less, preferably 10 nm or less, more preferably 5 nm or less. Surface A is the surface to be the cast film installation surface. When SRa (A) of surface A is larger than 20 nm, the smoothness of the surface in contact with the cast film support becomes insufficient when the cast film is installed. It is not preferable.

さらに、本発明のフィルムにおいて、A面の反対面(C面)の中心面平均粗さSRa(C)はSRa(A)より大きいこと、すなわち、粗面である必要があり、特に10〜50nm、さらに15〜30nmであることが好ましい。SRa(C)が10nm未満の場合、キャストフィルムと巻き取った際に、ブロッキングの発生やキャストフィルムの搬送性が悪化する等の問題が生じる場合がある。また、SRa(C)が50nmを超える場合には、キャストフィルム面への表面突起の転写、いわゆる裏写りが生じる恐れがあり、SRa(C)がSRa(A)と同じか小さい場合、上記不具合が顕著となり好ましくない。   Furthermore, in the film of the present invention, the center surface average roughness SRa (C) of the opposite surface (C surface) of the A surface is larger than SRa (A), that is, it needs to be a rough surface, particularly 10 to 50 nm. Furthermore, it is preferable that it is 15-30 nm. When SRa (C) is less than 10 nm, problems such as generation of blocking and deterioration of the transportability of the cast film may occur when the film is wound with the cast film. Further, when SRa (C) exceeds 50 nm, there is a risk of transfer of surface protrusions to the cast film surface, so-called show-through, and when SRa (C) is the same as or smaller than SRa (A), Is not preferable.

本発明のポリエステルフィルムのSRaを前述の範囲とするには、不活性微粒子、例えばシリカ、炭酸カルシウム、カオリン、酸化チタン、酸化アルミニウム、硫酸バリウム、ゼオライト等の無機粒子、またはシリコーン樹脂、架橋ポリスチレン、アクリル樹脂等の有機粒子を単独または混合体でフィルム中に配合させることが好ましい。この場合、使用する粒子の平均粒径、添加量、さらに粒径分布は、本発明の要旨を逸脱しない限り、特に限定されるものではないが、平均粒径は0.1〜4.0μmの範囲、添加量は0.01〜3.0重量%の範囲、粒径分布はその分散が小さいことがそれぞれ好ましい。   In order to bring the SRa of the polyester film of the present invention into the above-mentioned range, inert fine particles such as silica, calcium carbonate, kaolin, titanium oxide, aluminum oxide, barium sulfate, inorganic particles such as zeolite, or silicone resin, crosslinked polystyrene, It is preferable to mix organic particles such as acrylic resin alone or in a mixture in the film. In this case, the average particle size, the amount added, and the particle size distribution of the particles used are not particularly limited as long as they do not depart from the gist of the present invention, but the average particle size is 0.1 to 4.0 μm. It is preferable that the range and addition amount are in the range of 0.01 to 3.0% by weight, and that the particle size distribution has a small dispersion.

本発明のポリエステルフィルムは、複数の層が積層された多層フィルムであることが必要である。片面を極めて平滑にして、最終的にキャストフィルムを平滑にし、同時に平滑面の反対面を粗面化することにより耐ブロッキング性を保持させようとするため、例えば2種2層や3種3層といった構成で表裏異粗度であることが必要である。さらには、例えば3種3層といった中間層と2つの表層とを相異なる原料配合とすることができるようなフィルム構成とすることにより、中間層に微粒子を配合しなくとも、表層にのみ微粒子を添加するだけで本発明の要旨を満足する場合があり、微粒子を起因とする異物の削減や生産コスト低減化等が可能となり、より望ましい(例えば、特許文献3等に記載がある)。   The polyester film of the present invention needs to be a multilayer film in which a plurality of layers are laminated. In order to maintain the blocking resistance by making one side extremely smooth, finally smoothing the cast film, and at the same time roughening the opposite surface of the smooth surface, for example, 2 types 2 layers or 3 types 3 layers It is necessary to have different roughness on the front and back sides in such a configuration. Furthermore, for example, by adopting a film configuration in which an intermediate layer such as three types and three layers and two surface layers can be blended with different raw materials, fine particles can be added only to the surface layer, even without adding fine particles to the intermediate layer. There are cases where the gist of the present invention is satisfied only by addition, and it is possible to reduce foreign substances caused by fine particles, reduce production costs, and the like, which is more desirable (for example, described in Patent Document 3).

本発明のフィルムを使用して製造される光学フィルムは、通常、非晶性熱可塑性組成物を用い、溶液キャスト法にてフィルム化される光学フィルムである。かくして得られた光学フィルムの支持体側表面の中心面平均粗さSRaは、0.1〜1.0nmの範囲であることが好ましい。記録媒体の大容量化のために、青色レーザーを使用したり、レンズの高度化に対応するためには極限の平滑性が要求されたりするため、上記範囲が好ましい。   The optical film produced using the film of the present invention is usually an optical film that is formed into a film by a solution casting method using an amorphous thermoplastic composition. The center surface average roughness SRa of the support-side surface of the optical film thus obtained is preferably in the range of 0.1 to 1.0 nm. The above range is preferable because a blue laser is used to increase the capacity of the recording medium and extreme smoothness is required to cope with the advancement of lenses.

本発明において、製造される光学フィルムの平均的な厚みは、光記録媒体の光透過層用として用いるのに好適な厚みである、20〜300μm、好ましくは50〜150μm、さらに好ましくは60〜110μmである。   In the present invention, the average thickness of the produced optical film is 20 to 300 μm, preferably 50 to 150 μm, more preferably 60 to 110 μm, which is suitable for use as a light transmission layer of an optical recording medium. It is.

また本発明において、光学フィルムの原料として用いる非晶性熱可塑性樹脂組成物としては、ポリカーボネートを用いるのが好ましい。ポリカーボネートは安価で、塩化メチレンなどの溶剤に可溶であり、現在、CDやDVDなどの材料として既に大量に使用されているからである。寸法変化率の違いによる反りや歪みなどを防ぐために、光透過層とそれを貼り合わせる基板は同一の材料であることが好ましい。   In the present invention, polycarbonate is preferably used as the amorphous thermoplastic resin composition used as a raw material for the optical film. This is because polycarbonate is inexpensive and soluble in solvents such as methylene chloride, and is currently used in large quantities as a material for CDs and DVDs. In order to prevent warping or distortion due to a difference in dimensional change rate, it is preferable that the light transmission layer and the substrate on which the light transmission layer is bonded are made of the same material.

本発明において、光学フィルムに好ましく用いることのできる芳香族ポリカーボネート樹脂としては特には限定しないが、例としては、主たる構成成分が、2,2−ビス(4−ヒドロキシフェニル)プロパン(ビスフェノールA)からなる繰り返し単位で構成される芳香族ポリカーボネートが好ましい。ここでいう主たる構成成分とは、ポリカーボネートの原料であるジヒドロキシ化合物のうち、50モル%以上をしめる化合物からなる繰り返し成分を指す。そのため、2,2−ビス(4−ヒドロキシフェニル)プロパン(ビスフェノールA)を単独で使用しても、また50%を超えない範囲で他のジヒドロキシ化合物を加えて共重合あるいは混合したものを用いることができる。ビスフェノールAの繰り返し単位は、80モル%以上が好ましく、より好ましくは90モル%以上、特には100モル%(すなわち単独)が好ましい。   In the present invention, the aromatic polycarbonate resin that can be preferably used in the optical film is not particularly limited, but as an example, the main constituent is 2,2-bis (4-hydroxyphenyl) propane (bisphenol A). The aromatic polycarbonate comprised by the repeating unit which becomes is preferable. The main component here refers to a repeating component composed of a compound that accounts for 50 mol% or more of the dihydroxy compound that is a raw material of polycarbonate. Therefore, even if 2,2-bis (4-hydroxyphenyl) propane (bisphenol A) is used alone, other dihydroxy compounds may be added or copolymerized or mixed within a range not exceeding 50%. Can do. The repeating unit of bisphenol A is preferably 80 mol% or more, more preferably 90 mol% or more, and particularly preferably 100 mol% (that is, alone).

本発明において、支持体のポリエステルフィルムにキャストされた光学フィルムを巻き取る際には、支持体フィルムのキャストフィルム面と反対側の面が、キャストフィルムに粗度転写しない限り、そのまま巻き取ってもよいが、念のために、キャストフィルムの表面に保護フィルムを貼り付けて巻き取ることが好ましい。保護フィルムとしては特に限定されないが、表面平滑性が比較的高いPETフィルムの保護フィルムを用いるのが好ましく、PETフィルムの表面に微粘着加工したものが好ましい。この場合の微粘着とは、一度貼合した保護フィルムを、光学フィルムを傷つけることなく、かつ接着剤が光学フィルム上に残ることなく剥離可能なものをいう。   In the present invention, when the optical film cast on the polyester film of the support is wound up, the surface opposite to the cast film surface of the support film may be wound up as it is unless it is transferred to the cast film. Although it is good, as a precaution, it is preferable to attach a protective film on the surface of the cast film and wind it up. Although it does not specifically limit as a protective film, It is preferable to use the protective film of PET film with comparatively high surface smoothness, and what carried out the fine adhesion process on the surface of PET film is preferable. The slight adhesion in this case means that the protective film once bonded can be peeled without damaging the optical film and without the adhesive remaining on the optical film.

以下、本発明のフィルムの製造方法に関して具体的に説明するが、本発明の効果を満足する限り、本発明は以下の例示に特に限定されるものではない。   Hereinafter, although the manufacturing method of the film of this invention is demonstrated concretely, as long as the effect of this invention is satisfied, this invention is not specifically limited to the following illustrations.

公知の手法により乾燥したポリエステルチップを溶融積層用押出装置に供給し、それぞれのポリマーの融点以上である温度に加熱し溶融する。次いで、溶融したポリマーをダイから押出し、回転冷却ドラム上でガラス転移温度以下の温度になるように急冷固化し、実質的に非晶状態の未配向シートを得る。すなわち、2または3台以上の押出機、2層以上のマニホールドまたは合流ブロックを用いて、最外層を構成するフィルム層、中間層を構成するフィルム層を積層し、口金から2層以上のシートを押し出し、キャスティングロールで冷却して未延伸フィルムを形成する。この場合、シートの平面性を向上させるため、シートと回転冷却ドラムとの密着性を高めることが好ましく、本発明においては静電印加密着法および/または液体塗布密着法が好ましく採用される。   A polyester chip dried by a known method is supplied to an extruder for melt lamination and heated to a temperature equal to or higher than the melting point of each polymer to melt. Next, the molten polymer is extruded from a die and rapidly cooled and solidified on a rotary cooling drum so that the temperature is equal to or lower than the glass transition temperature to obtain a substantially amorphous unoriented sheet. That is, using two or three or more extruders, two or more manifolds or a merge block, a film layer constituting the outermost layer and a film layer constituting the intermediate layer are laminated, and two or more sheets are formed from the die. Extruded and cooled with a casting roll to form an unstretched film. In this case, in order to improve the flatness of the sheet, it is preferable to improve the adhesion between the sheet and the rotary cooling drum. In the present invention, an electrostatic application adhesion method and / or a liquid application adhesion method is preferably employed.

またこの場合、溶融押出の際に、樹脂中に含まれる異物を除去するために高精度濾過を行うことが好ましい。高精度濾過に用いられる濾材としては、ステンレスの焼結体が好ましい。   In this case, it is preferable to perform high-precision filtration in order to remove foreign substances contained in the resin during melt extrusion. The filter medium used for high-precision filtration is preferably a stainless sintered body.

このようにして得られたシートを2軸方向に延伸してフィルム化する。延伸条件について具体的に述べると、前記未延伸シートを好ましくは縦方向に70〜145℃で2〜6倍に延伸し、縦1軸延伸フィルムとした後、横方向に90〜160℃で2〜6倍延伸を行い、150〜240℃で1〜600秒間熱処理を行うことが好ましい。さらにこの際、熱処理の最高温度ゾーンおよび/または熱処理出口のクーリングゾーンにおいて、縦方向および/または横方向に0.1〜20%弛緩する方法が好ましい。また、必要に応じて再縦延伸、再横延伸を付加することも可能である。   The sheet thus obtained is stretched in the biaxial direction to form a film. Specifically describing the stretching conditions, the unstretched sheet is preferably stretched 2 to 6 times at 70 to 145 ° C. in the longitudinal direction to form a longitudinal uniaxially stretched film, and then 2 to 90 to 160 ° C. in the lateral direction. It is preferable to perform ~ 6 times stretching and heat treatment at 150 to 240 ° C for 1 to 600 seconds. Further, at this time, a method of relaxing 0.1 to 20% in the longitudinal direction and / or the transverse direction in the maximum temperature zone of the heat treatment and / or the cooling zone at the heat treatment outlet is preferable. Further, it is possible to add re-longitudinal stretching and re-lateral stretching as necessary.

さらに本発明のフィルムは、キズの発生を嫌うので、同時二軸延伸装置を用いて延伸することも好ましい。同時二軸延伸装置で有ればどのような装置でもよいが、リニアモーターで走行する装置が好ましく用いられる。   Furthermore, since the film of the present invention dislikes the generation of scratches, it is also preferable to stretch using a simultaneous biaxial stretching apparatus. Any apparatus may be used as long as it is a simultaneous biaxial stretching apparatus, but an apparatus that travels with a linear motor is preferably used.

また本発明のポリエステルフィルムは、本発明の効果を損なわない範囲であれば、その要求特性に応じて必要な特性、例えば帯電防止性、耐候性および表面硬度の向上のため、必要に応じて縦延伸終了後、横延伸のテンター入口前にコートをしてテンター内で乾燥する、いわゆるインラインコート法を行ってもよい。また、フィルム製造後にオフラインコートで各種のコートを行ってもよい。このようなコートは片面、両面のいずれでもよい。コーティングの材料としては、オフラインコーティングの場合は水系および/または溶媒系のいずれでもよいが、インラインコーティングの場合は水系または水分散系が好ましい。   In addition, the polyester film of the present invention has a length that does not impair the effects of the present invention. After the stretching, a so-called in-line coating method in which coating is performed before the entrance of the tenter for lateral stretching and drying in the tenter may be performed. Various coatings may be performed by offline coating after film production. Such a coat may be either single-sided or double-sided. The coating material may be either water-based and / or solvent-based for offline coating, but is preferably water-based or water-dispersed for in-line coating.

さらに、本発明のポリエステルフィルムには、本発明の効果を損なわない範囲であれば、他の熱可塑性樹脂、例えばポリエチレンナフタレート、ポリトリメチレンテレフタレート等を混合することができる。また、紫外線吸収剤、酸化防止剤、界面活性剤、顔料、蛍光増白剤等を混合することができる。   Furthermore, other thermoplastic resins such as polyethylene naphthalate and polytrimethylene terephthalate can be mixed in the polyester film of the present invention as long as the effects of the present invention are not impaired. Further, an ultraviolet absorber, an antioxidant, a surfactant, a pigment, a fluorescent brightening agent, and the like can be mixed.

本発明において、光学フィルムの平滑性をさらに高くする方法としては、本発明のフィルムの平滑面側に、他の樹脂をコーティングする方法、表面に金属を蒸着もしくはめっきを行う方法、接着剤などを介して別のシートもしくはフィルムあるいは金属板を貼り合わせる方法、研磨による方法、物理的もしくは化学的処理により平滑にする方法等が挙げられるが、表面性の制御が比較的容易な樹脂のコーティングによる方法が好ましい。   In the present invention, as a method for further increasing the smoothness of the optical film, a method of coating another resin on the smooth surface side of the film of the present invention, a method of depositing or plating a metal on the surface, an adhesive, etc. A method of laminating another sheet or film or a metal plate, a method of polishing, a method of smoothing by physical or chemical treatment, etc., but a method of coating a resin whose surface property is relatively easy to control Is preferred.

さらにコーティング層は、支持体を搬送しても傷がつきにくいようにコーティング層の表面の硬度(例えば鉛筆硬度等の指標)が高いことが好ましい。このようなコーティング層を形成する方法としては、既知の樹脂を用いてハードコート層を形成する方法等を用いることができる。   Furthermore, it is preferable that the coating layer has a high surface hardness (for example, an index such as pencil hardness) so that the coating layer is hardly damaged even when the support is conveyed. As a method of forming such a coating layer, a method of forming a hard coat layer using a known resin can be used.

かくして得られた支持体フィルムに、溶液塗布法または溶液流延法に代表される溶液キャスト法を用いてキャストする。その際該樹脂溶液を乾燥して支持体と反対面に保護フィルムを貼り合わせて巻き取ることが好ましい。かくして得られた光学フィルムを用い、光透過層となるようディスクに加工してDVDを作成することができる。   The support film thus obtained is cast using a solution casting method typified by a solution coating method or a solution casting method. At that time, it is preferable to dry the resin solution, and attach a protective film on the surface opposite to the support to wind it. Using the optical film thus obtained, a DVD can be produced by processing it into a disc so as to form a light transmission layer.

本発明によれば、DVD用の光透過層作成の際の工程紙として用いた際に優れた効果を有するポリエステルフィルムを提供することができ、その工業的価値は高い。   ADVANTAGE OF THE INVENTION According to this invention, the polyester film which has the outstanding effect when it uses as process paper at the time of the light transmission layer preparation for DVD can be provided, The industrial value is high.

以下、本発明を実施例によりさらに詳細に説明するが、本発明はその要旨を越えない限り、以下の実施例に限定されるものではない。なお、種々の諸物性、特性は以下のように測定、または定義されたものである。実施例中、「%」は「重量%」を意味する。   EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to a following example, unless the summary is exceeded. Various physical properties and characteristics are measured or defined as follows. In the examples, “%” means “% by weight”.

(1)中心面平均粗さの測定
3cm角のフィルム試料の表面にAl蒸着を行い、直接位相検出干渉法、いわゆる2光束干渉法を用いた非接触式3次元粗さ計(マイクロマップ社製512)で、測定波長:554nm、対物レンズ倍率:20倍の条件にて、突起高さ分布曲線より、232μm×177μmの測定領域におけるA面、およびC面の中心面平均粗さSRaを50点にわたり測定し、50点のSRa値を平均して、フィルムのSRaを算出した。
(1) Measurement of center plane average roughness Non-contact type three-dimensional roughness meter (manufactured by Micromap) using Al deposition on the surface of a 3 cm square film sample and using direct phase detection interferometry, so-called two-beam interferometry 512), the average surface roughness SRa of the A plane and the C plane in the measurement area of 232 μm × 177 μm is 50 points from the projection height distribution curve under the conditions of the measurement wavelength: 554 nm and the objective lens magnification: 20 times. The SRa value of the film was calculated by averaging the 50 SRa values.

(ポリエステルチップの製造法)
ジメチルテレフタレート100部、エチレングリコール70部、および酢酸カルシウム一水塩0.07部を反応器にとり、加熱昇温すると共にメタノール留去させエステル交換反応を行い、反応開始後、約4時間半を要して230℃に昇温し、実質的にエステル交換反応を終了した。次に燐酸0.04部および三酸化アンチモン0.035部を添加し、常法に従って重合した。すなわち、反応温度を徐々に上げて、最終的に280℃とし、一方、圧力は徐々に減じて、最終的に0.05mmHgとした。4時間後、反応を終了し、常法に従い、チップ化してポリエステルAを得た。
(Polyester chip manufacturing method)
Take 100 parts of dimethyl terephthalate, 70 parts of ethylene glycol, and 0.07 part of calcium acetate monohydrate in a reactor, heat up and evaporate methanol to conduct transesterification, and take about 4 and a half hours after starting the reaction. The temperature was raised to 230 ° C. to substantially complete the transesterification reaction. Next, 0.04 part of phosphoric acid and 0.035 part of antimony trioxide were added and polymerized in accordance with a conventional method. That is, the reaction temperature was gradually raised to finally 280 ° C., while the pressure was gradually reduced to finally 0.05 mmHg. After 4 hours, the reaction was completed, and a chip was obtained according to a conventional method to obtain polyester A.

上記ポリエステルAを製造する際、平均粒径0.7μmの炭酸カルシウムを20000ppm添加し、ポリエステルBを得た。   When manufacturing the said polyester A, 20000 ppm of calcium carbonate with an average particle diameter of 0.7 micrometer was added, and the polyester B was obtained.

さらに、上記ポリエステルAを製造する際、平均粒径2.4μmの非晶質シリカを20000ppm添加し、ポリエステルCを得た。   Furthermore, when manufacturing the said polyester A, 20000 ppm of amorphous silica with an average particle diameter of 2.4 micrometers was added, and the polyester C was obtained.

さらに、上記ポリエステルAを製造する際、平均粒径0.2μmの酸化アルミニウムを20000ppm添加し、ポリエステルDを得た。   Furthermore, when manufacturing the said polyester A, 20000 ppm of aluminum oxide with an average particle diameter of 0.2 micrometer was added, and the polyester D was obtained.

(ポリエステルフィルムの製造)
上記ポリエステルA、Dをそれぞれ50%、50%の割合で混合した混合原料1をA層の原料とし、ポリエステルA、Cをそれぞれ95%、5%の割合で混合した混合原料2をC層の原料とし、2台の押出機に各々を供給し、各々285℃で溶融した後、A層およびC層を最外層(表層)20℃に冷却したキャスティングドラム上に、2種2層の層構成で共押出し冷却固化させて無配向シートを得た。次いで、90℃にて縦方向に3倍延伸した後、テンター内で予熱工程を経て100℃で4倍の横延伸、230℃で10秒間の熱処理を行い、このフィルムの巻き上げ直前のフィルム厚みを非接触式のオンライン厚さ計にて横方向にスキャンしながら厚みムラ実測し、測定した厚みパターンに応じて口金の間隔を調整し、厚みムラを制御した125μmのポリエステルフィルムを得た。なお、各層の厚さ、表面粗さ等は下記表1に示すとおりであった。
(Manufacture of polyester film)
The mixed raw material 1 in which the polyesters A and D are mixed at a ratio of 50% and 50%, respectively, is used as the raw material for the A layer, and the mixed raw material 2 in which the polyesters A and C are mixed at a ratio of 95% and 5%, respectively. Each is supplied to two extruders as raw materials, melted at 285 ° C each, and then the layer configuration of two types and two layers on a casting drum in which the A layer and the C layer are cooled to the outermost layer (surface layer) 20 ° C Were coextruded and cooled and solidified to obtain a non-oriented sheet. Next, the film was stretched three times in the longitudinal direction at 90 ° C., then subjected to a preheating step in a tenter, transversely stretched four times at 100 ° C., and subjected to heat treatment at 230 ° C. for 10 seconds. The thickness unevenness was actually measured while scanning in the horizontal direction with a non-contact type on-line thickness meter, the interval between the caps was adjusted according to the measured thickness pattern, and a 125 μm polyester film with controlled thickness unevenness was obtained. The thickness and surface roughness of each layer were as shown in Table 1 below.

得られたポリエステルフィルムの平滑側の表面に、アクリル樹脂を塗布し、紫外線照射により硬化させて5μmのハードコート層を設けた。次に溶媒としてジクロロメタンを用いて、ポリカーボネートの20重量%溶液を調合し、当該ポリカーボネート溶液を上記支持体に塗布し、乾燥を行い、PETと反対の面に保護フィルムを挟んで巻き取った。かくして得られた100μmの光学フィルムを光透過層として用いてDVDを作成し信号特性を調べたところ良好な特性が得られた。   An acrylic resin was applied to the smooth surface of the obtained polyester film and cured by ultraviolet irradiation to provide a 5 μm hard coat layer. Next, using a dichloromethane as a solvent, a 20% by weight solution of polycarbonate was prepared, the polycarbonate solution was applied to the support, dried, and wound with a protective film sandwiched between the surface opposite to PET. When a DVD was prepared using the optical film of 100 μm thus obtained as a light transmission layer and the signal characteristics were examined, good characteristics were obtained.

(実施例2〜3)
実施例1で原料配合を表1のように変更した点、および実施例1と同様な方法にて厚みムラを制御して表1の厚みムラとした以外、実施例1と同様な方法にて125μmのポリエステルフィルムを得た。得られたポリエステルフィルムは、表1に示したような結果となり、実施例1と同様にDVDとしたところ良好な特性を示した。
(Examples 2-3)
In the same manner as in Example 1 except that the raw material composition in Example 1 was changed as shown in Table 1 and the thickness unevenness was controlled by the same method as in Example 1 to obtain the thickness unevenness in Table 1. A 125 μm polyester film was obtained. The obtained polyester film showed the results as shown in Table 1. When it was made into a DVD as in Example 1, it showed good characteristics.

(実施例4)
表1に示す原料配合にて各層の混合原料を作成し、3台の押出機に各々を供給し、各々285℃で溶融した後、A層およびC層を最外層(表層)、B層を中間層として、20℃に冷却したキャスティングドラム上に、3種3層の層構成で共押出し冷却固化させて無配向シートを得た以外、実施例1と同様な方法にて製造し、ポリエステルフィルムを得た。なお、ポリエステルフィルムの各層の厚さは表1に示すとおりであった。実施例1と同様良好な特性を示した。
Example 4
After preparing the mixed raw material of each layer by the raw material composition shown in Table 1, supplying each to three extruders and melting each at 285 ° C., the A layer and the C layer are the outermost layer (surface layer), and the B layer is As an intermediate layer, a polyester film was produced in the same manner as in Example 1 except that a non-oriented sheet was obtained by coextrusion and solidification on a casting drum cooled to 20 ° C. in a three-layer / three-layer structure. Got. The thickness of each layer of the polyester film was as shown in Table 1. Good characteristics as in Example 1 were exhibited.

(比較例1〜2)
A層、B層、C層の原料配合、および厚みムラを下記表2に示すとおりとした以外、実施例4と同様にして製造し、ポリエステルフィルムを得た。実施例1と同様にしてDVDを作成したが、比較例1では、表面の凹凸が大きく良好な信号特性が得られなかった。一方比較例2では、シワが入ったりしてフィルムが良好に巻き取れなかった。
(Comparative Examples 1-2)
A polyester film was obtained in the same manner as in Example 4 except that the raw material composition of layer A, layer B and layer C, and thickness unevenness were as shown in Table 2 below. A DVD was produced in the same manner as in Example 1. However, in Comparative Example 1, the surface irregularities were large and good signal characteristics could not be obtained. On the other hand, in Comparative Example 2, wrinkles occurred and the film could not be wound well.

Figure 2005190529
Figure 2005190529

本発明のフィルムは、DVDの高密度化のために必要な薄膜化された光透過保護層の作成の際に用いられる工程紙に好適に使用することができる。   The film of the present invention can be suitably used for process papers used in the production of a thinned light-transmitting protective layer necessary for increasing the density of DVD.

Claims (1)

高密度DVD光透過保護層の工程紙として使用されるポリエステルフィルムであって、一方のフィルム面(A面)の中心面平均粗さ(SRa(A))が20nm以下であり、もう一方のフィルム面(C面)の中心面平均粗さ(SRa(C))がSRa(A)よりも大きいことを特徴とする積層ポリエステルフィルム。
A polyester film used as a process paper for a high-density DVD light-transmitting protective layer, wherein one film surface (A surface) has a center surface average roughness (SRa (A)) of 20 nm or less, and the other film. A laminated polyester film characterized in that the center surface average roughness (SRa (C)) of the surface (C surface) is larger than SRa (A).
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007050631A (en) * 2005-08-19 2007-03-01 Mitsubishi Polyester Film Copp Substrate film for manufacturing plastic film by cast method

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000043214A (en) * 1998-07-28 2000-02-15 Teijin Ltd Laminated biaxially orientated polyester film
JP2001341265A (en) * 2000-06-06 2001-12-11 Teijin Ltd Laminated biaxially oriented polyester film
JP2003291289A (en) * 2002-04-01 2003-10-14 Teijin Dupont Films Japan Ltd Biaxially oriented laminated polyester film
JP2003326543A (en) * 2002-05-09 2003-11-19 Kanegafuchi Chem Ind Co Ltd Optical film and manufacturing method therefor

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000043214A (en) * 1998-07-28 2000-02-15 Teijin Ltd Laminated biaxially orientated polyester film
JP2001341265A (en) * 2000-06-06 2001-12-11 Teijin Ltd Laminated biaxially oriented polyester film
JP2003291289A (en) * 2002-04-01 2003-10-14 Teijin Dupont Films Japan Ltd Biaxially oriented laminated polyester film
JP2003326543A (en) * 2002-05-09 2003-11-19 Kanegafuchi Chem Ind Co Ltd Optical film and manufacturing method therefor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007050631A (en) * 2005-08-19 2007-03-01 Mitsubishi Polyester Film Copp Substrate film for manufacturing plastic film by cast method

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