JPH04110148A - Mat polyester film - Google Patents

Mat polyester film

Info

Publication number
JPH04110148A
JPH04110148A JP2228953A JP22895390A JPH04110148A JP H04110148 A JPH04110148 A JP H04110148A JP 2228953 A JP2228953 A JP 2228953A JP 22895390 A JP22895390 A JP 22895390A JP H04110148 A JPH04110148 A JP H04110148A
Authority
JP
Japan
Prior art keywords
film
raw material
layers
polyester film
polyester
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2228953A
Other languages
Japanese (ja)
Inventor
Satoyuki Kotani
小谷 智行
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Diafoil Co Ltd
Original Assignee
Diafoil Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Diafoil Co Ltd filed Critical Diafoil Co Ltd
Priority to JP2228953A priority Critical patent/JPH04110148A/en
Publication of JPH04110148A publication Critical patent/JPH04110148A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a laminated polyester film having both of matting effect and tenacity by using a polyester film having certain physical properties formed by laminating at least two or more layers by co-extrusion. CONSTITUTION:In a composite film wherein two or more layers are laminated by co-extrusion, a mat polyester film wherein the glossiness Gs (60 deg.) of the single surface (A-surface) of the film is 10-90% and the thickness ratio of the layer constituting the A-surface to the whole of the film is 0.4 or less and the sum of the breaking strengths in the longitudinal and lateral. directions of the film is 36 kg/mm<2> or more is used. For example, a raw material A1 composed of polyethylene terephthalate containing 0.05wt.% of amorphous silica particles and a raw material B1 composed of polyethylene terephthalate containing 2.7wt.% of said silica particles are respectively dried and compounded as a three-layer structure wherein the raw material B1 is used as outer layers and the raw material A1 is used as an inner layer and the thickness ratio B1/A1/B1 of the layers is 1.25/22.5/1.25 using separate melting extruders to prepare an amorphous sheet which is, in turn, stretched to be thermally fixed.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は優れた艶消し効果を有し、かつ強靭性に優れた
積層ポリエステルフィルムに関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a laminated polyester film having an excellent matte effect and excellent toughness.

〔従来の技術および発明が解決しようとする課題〕艶消
しポリエステルフィルムは、優れた強靭性、耐久性、耐
熱性、透明性および耐薬品性等を有することから、転写
箔用、建材用、表示板用、ラベル用等の広い用途に使用
されている。
[Prior art and problems to be solved by the invention] Matte polyester films have excellent toughness, durability, heat resistance, transparency, and chemical resistance, so they are used for transfer foils, building materials, and displays. It is used for a wide range of purposes such as plates and labels.

艶消しポリエステルフィルムを得るには、ポリエステル
に不活性な粒子を添加し二軸延伸する方法が有効である
。しかしながら、フィルムの光沢度Gs (60°)が
低いほど、すなわち艶消し効果が大きいほど、フィルム
の強靭性が消失する。
An effective method for obtaining a matte polyester film is to add inert particles to polyester and then biaxially stretch the film. However, the lower the gloss Gs (60°) of the film, ie the greater the matting effect, the less toughness the film loses.

従って、比較的高強度が要求される用途、例えば転写箔
用途では、艶消しフィルムを用いることができなかった
Therefore, matte films cannot be used in applications that require relatively high strength, such as transfer foil applications.

(課題を解決するための手段〕 本発明者は上記課題に鑑み、鋭意検討した結果、少な(
とも2層以上が共押出により積層されてなる、ある特定
の物性を有するポリエステルフィルムが、艶消し効果と
強靭性とを併せて有することを見いだし、本発明を完成
するに至った。
(Means for Solving the Problems) In view of the above problems, the inventors of the present invention have made extensive studies and found that a small amount (
It was discovered that a polyester film having certain physical properties, which is formed by laminating two or more layers by coextrusion, has both a matte effect and toughness, and the present invention was completed.

すなわち本発明の要旨は、共押出により2層以上積層し
た複合フィルムであって、フィルムの片面(A面)の光
沢度Os (60°)が10〜90%であり、A面を構
成する層のフィルム全体に対する厚み比が0.4以下で
あり、かつフィルムの縦方向および横方向の破断強度の
和が361g / Wz以上であることを特徴とする艶
消しポリエステルフィルムに存する。
That is, the gist of the present invention is to provide a composite film in which two or more layers are laminated by coextrusion, in which the glossiness Os (60°) of one side (A side) of the film is 10 to 90%, and the layer constituting the A side is The matte polyester film has a thickness ratio of 0.4 or less to the entire film, and a sum of the breaking strength in the longitudinal direction and the transverse direction of the film is 361 g/Wz or more.

以下、本発明を更に詳細に説明する。The present invention will be explained in more detail below.

本発明でいうポリエステルとは、テレフタル酸またはそ
のエステルと、エチレングリコールを主たる出発原料と
して得られるポリエステルを指すが、他の第三成分を含
有していてもよい。この場合、ジカルボン酸成分として
、例えばイソフタル酸、フタル酸、2,6−ナフタレン
ジカルボン酸、テレフタル酸、アジピン酸、セバシン酸
、p−オキシエトキシ安息香酸等のオキシカルボン酸成
分の一種または二種以上を用いることが可能である。
The term "polyester" used in the present invention refers to a polyester obtained using terephthalic acid or its ester and ethylene glycol as main starting materials, but it may contain other third components. In this case, the dicarboxylic acid component is one or more of oxycarboxylic acid components such as isophthalic acid, phthalic acid, 2,6-naphthalene dicarboxylic acid, terephthalic acid, adipic acid, sebacic acid, and p-oxyethoxybenzoic acid. It is possible to use

グリコール成分としては、エチレングリコール、プロピ
レングリコール、ブタンジオール、1,4シクロヘキサ
ンジメタツール、ネオペンチルグリコール等の一種また
は二種以上を用いることができる。いずれにしても本発
明のポリエステルは繰り返し構造単位の80%以上がエ
チレンテレフタレート単位を有するポリエステルである
ことが好ましい。
As the glycol component, one or more of ethylene glycol, propylene glycol, butanediol, 1,4 cyclohexanedimetatool, neopentyl glycol, etc. can be used. In any case, the polyester of the present invention is preferably a polyester in which 80% or more of the repeating structural units have ethylene terephthalate units.

また、ポリエステルに任意の添加剤、例えば、熱安定剤
、ブロッキング防止剤、酸化防止剤、着色剤、帯電防止
剤、紫外線吸収剤などを含有させてもよい。
Further, the polyester may contain arbitrary additives such as a heat stabilizer, an antiblocking agent, an antioxidant, a coloring agent, an antistatic agent, and an ultraviolet absorber.

さらに、上記ポリエステルに対し、ポリエステル以外の
ポリマー、例えばポリカーボネート、ポリオレフィン、
ポリアミド等を本発明の要旨を越えない範囲、例えば全
体の30wt%以下であれば添加、混合してもよい。こ
のように、他種のポリマーを添加、混合することにより
フィルム表面を粗面化し、好適な表面光沢性、筆記性を
与える方法も、本発明を具現化するための一手法として
挙げられる。
Furthermore, in addition to the above polyester, polymers other than polyester, such as polycarbonate, polyolefin,
Polyamide or the like may be added or mixed as long as it does not exceed the gist of the present invention, for example, 30 wt% or less of the total. As described above, a method of roughening the film surface by adding and mixing other kinds of polymers to impart suitable surface gloss and writability is also mentioned as one method for realizing the present invention.

フィルムに易滑性、表面光沢性等を付与するために、有
機、無機等の微粒子を含有させることも好ましく、必要
に応じて安定剤、着色剤、酸化防止剤、消泡剤、静電防
止剤等の添加剤をフィルム中に含有するものであっても
よい。フィルムに滑り性、表面光沢性を付与する微粒子
としては、カオリン、クレー、炭酸カルシウム、酸化ケ
イ素、テレフタレ酸カルシウム、酸化アルミニウム、酸
化チタン、リン酸カルシウム、フン化リチウム、カーボ
ンブラック等の公知の不活性外部粒子、ポリエステル樹
脂の溶融製膜に際して不溶な高融点有機化合物、架橋ポ
リマーおよびポリエステル合成時に使用する金属化合物
触媒、例えばアルカリ金属化合物、アルカリ土類金属化
合物などによってポリエステル製造時にポリマー内部に
形成される内部粒子が挙げられる。
In order to impart slipperiness, surface gloss, etc. to the film, it is also preferable to contain organic, inorganic, etc. fine particles, and if necessary, stabilizers, colorants, antioxidants, antifoaming agents, and antistatic agents. The film may also contain additives such as additives. Fine particles that impart slipperiness and surface gloss to the film include known inert particles such as kaolin, clay, calcium carbonate, silicon oxide, calcium terephthalate, aluminum oxide, titanium oxide, calcium phosphate, lithium fluoride, and carbon black. Internal particles formed inside the polymer during polyester production due to particles, insoluble high-melting point organic compounds during melt film formation of polyester resin, crosslinked polymers, and metal compound catalysts used during polyester synthesis, such as alkali metal compounds and alkaline earth metal compounds. Examples include particles.

本発明のフィルムに表面光沢性を付与するために含有さ
せる微粒子としては、酸化ケイ素の微粒子を主体とする
ものが好ましく、該粒子の含有により、所望の表面光沢
性、筆記性が効率良く付与される。
The fine particles contained in the film of the present invention for imparting surface gloss are preferably those mainly composed of silicon oxide fine particles, and the inclusion of the particles efficiently imparts desired surface gloss and writability. Ru.

上記態様において、酸化ケイ素微粒子に加えて他の微粒
子、例えば酸化チタンを含有することも好ましいS様の
一つである。
In the above embodiment, it is also a preferable S type to contain other fine particles, such as titanium oxide, in addition to silicon oxide fine particles.

本発明のフィルムにおいて、表面光沢性を付与する層に
含有させる微粒子の平均粒径は、通常、0.5〜10μ
mの範囲である。平均粒径が0.5μm未満の場合、所
望の表面光沢性を持つフィルムが得られず不適当である
。また、平均粒径が10μmを超えると、フィルム表面
の凸凹が大き過ぎ、実用的でない。フィルム中に含まれ
る微粒子の平均粒径は好ましくは1.0〜108m1さ
らに好ましくは1.5〜10μm、特に好ましくは2.
0〜7.0μmの範囲である。
In the film of the present invention, the average particle size of the fine particles contained in the layer imparting surface gloss is usually 0.5 to 10 μm.
m range. If the average particle size is less than 0.5 μm, it is not suitable because a film with the desired surface gloss cannot be obtained. Moreover, if the average particle diameter exceeds 10 μm, the unevenness of the film surface will be too large to be practical. The average particle size of the fine particles contained in the film is preferably 1.0 to 108 m1, more preferably 1.5 to 10 m, and particularly preferably 2.0 m to 108 m.
It is in the range of 0 to 7.0 μm.

本発明のフィルムにおいて、表面光沢性を付与する層に
含有させる微粒子の量は、好ましくは0゜2〜10重量
%、さらに好ましくは、0.2〜7.0重量%、特に好
ましくは0.2〜5.0重量%の範囲である。
In the film of the present invention, the amount of fine particles contained in the layer imparting surface gloss is preferably 0.2 to 10% by weight, more preferably 0.2 to 7.0% by weight, particularly preferably 0.2 to 10% by weight. It ranges from 2 to 5.0% by weight.

本発明のポリエステルフィルムの極限粘度は、好ましく
は0.50以上、さらに好ましくは0.60以上である
。フィルムの極限粘度が0.50未満の場合、十分な機
械的強度を有するフィルムが得られず好ましくない。
The intrinsic viscosity of the polyester film of the present invention is preferably 0.50 or more, more preferably 0.60 or more. If the intrinsic viscosity of the film is less than 0.50, it is not preferable because a film with sufficient mechanical strength cannot be obtained.

本発明のフィルムの片面(A面)の光沢度Gs(60°
)は10〜90%の範囲であることが必要である。Gs
(60°)が10%未満では、フィルム表面が粗過ぎ、
実用的でない。一方、Qs(60’)が90%を超える
場合、艷消し効果が不十分である。A面の光沢度0s(
60°)は好ましくは、10〜60%、さらに好ましく
は10〜40%の範囲である。
Glossiness Gs (60°) of one side (side A) of the film of the present invention
) must be in the range of 10 to 90%. Gs
(60°) is less than 10%, the film surface is too rough;
Not practical. On the other hand, when Qs(60') exceeds 90%, the erasing effect is insufficient. Glossiness of side A is 0s (
60°) is preferably in the range of 10 to 60%, more preferably 10 to 40%.

本発明のフィルムにおいて、フィルムの縦方向および横
方向の破断強度の和は、36kg/ms2以上である。
In the film of the present invention, the sum of the breaking strength in the longitudinal direction and the transverse direction of the film is 36 kg/ms2 or more.

フィルムの縦方向および横方向の破断強度の和が36b
/m2未満の場合、機械的強度が不十分であり実用に供
することができない。フィルムの縦方向および横方向の
破断強度の和は、好ましくは、40kg/wm2以上さ
らに好ましくは、45呟/ w ”以上、特に好ましく
は50kg/鶴2以上である。また本発明のフィルムは
、縦方向または横方向に高強度化されているフィルムで
あってもよい。
The sum of the breaking strength in the longitudinal and transverse directions of the film is 36b
If it is less than /m2, the mechanical strength is insufficient and it cannot be put to practical use. The sum of the breaking strengths of the film in the longitudinal and transverse directions is preferably 40 kg/wm2 or more, more preferably 45 kg/w" or more, particularly preferably 50 kg/wm2 or more. The film of the present invention also has the following properties: The film may be highly strengthened in the vertical or horizontal direction.

本発明のフィルムは少なくとも2層以上が共押出により
積層されていることが必要である。通常の単層フィルム
ではフィルム表面の光沢度Gs(60’)とフィルムの
機械的強度を共に改良することができない。
The film of the present invention needs to have at least two layers laminated by coextrusion. With ordinary single-layer films, it is not possible to improve both the glossiness Gs (60') of the film surface and the mechanical strength of the film.

A面を構成する層のフィルム全体に対する厚み比は、0
.4以下である。かかる厚み比は、好ましくは、0.3
以下、さらに好ましくは0.2以下である。厚み比が0
.4を超えると、積層によるフィルム強度の改良効果が
小さいため好ましくない。
The thickness ratio of the layer constituting side A to the entire film is 0.
.. 4 or less. Such a thickness ratio is preferably 0.3
Below, it is more preferably 0.2 or below. Thickness ratio is 0
.. If it exceeds 4, it is not preferable because the effect of improving film strength by lamination is small.

本発明のフィルムの厚さは特に限定されないが、転写箔
用、建材用、ラベル用、表示板用等のへ一スフィルムと
して好ましく用いられる厚さは5〜500μm、さらに
好ましくは、5〜200μm、特に好ましくは5〜75
μmの範囲である。
The thickness of the film of the present invention is not particularly limited, but the thickness preferably used as a base film for transfer foils, building materials, labels, display boards, etc. is 5 to 500 μm, more preferably 5 to 200 μm. , particularly preferably 5 to 75
It is in the μm range.

次に本発明のフィルムの製造法を具体的に説明するが、
本発明の構成要件を満足する限り、以下の例示に特に限
定されるものではない。
Next, the method for manufacturing the film of the present invention will be specifically explained.
As long as the constituent requirements of the present invention are satisfied, the invention is not particularly limited to the following examples.

表面光沢性を付与するために、無機粒子等を必要に応じ
て通量含有するポリエステル原料(alと、別途調製し
たポリエステル原料(′b)とを、それぞれ別々にホン
パードライヤー、パドルドライヤーオーブン等の通常用
いられる乾燥機または真空乾燥機等を用いて乾燥した後
、別々の押出機により200〜320℃で溶融押出し、
共押出法により、原料(alで構成される層が少なくと
も片面において表層となるよう複合化し、キャスティン
グドラム上で冷却固化させて、2層以上の層からなる無
定形シートを形成する。この際、常法の静電印加法を用
いると該無定形シートの厚さ斑が向上するので好ましい
In order to impart surface gloss, a polyester raw material (al) containing inorganic particles and the like as necessary and a separately prepared polyester raw material ('b) are separately heated in a homper dryer, paddle dryer oven, etc. After drying using a commonly used dryer or vacuum dryer, etc., melt extrusion at 200 to 320 ° C. using a separate extruder,
By a coextrusion method, the raw material (Al) is composited so that the layer composed of the material becomes a surface layer on at least one side, and is cooled and solidified on a casting drum to form an amorphous sheet consisting of two or more layers. At this time, It is preferable to use a conventional electrostatic application method because it improves the thickness unevenness of the amorphous sheet.

次いで得られた無定形シートを縦および横方向に面積倍
率で13倍以上延伸して、二軸配向ポリエステルフィル
ムとし、さらに210〜250℃の範囲の温度で熱処理
する。
The obtained amorphous sheet is then stretched in the longitudinal and transverse directions at an area magnification of 13 times or more to form a biaxially oriented polyester film, and further heat treated at a temperature in the range of 210 to 250°C.

熱処理工程において、熱処理の最高温度のゾーンおよび
/または熱処理出口のクリーングゾーンにて横方向およ
び/または縦方向に0.1〜30%の弛緩を行うことも
本発明においては好ましい態様の1つである。特に横方
法においては、5〜30%の弛緩を行うことが好ましい
。また、熱処理工程において、二段熱処理を行ってもよ
い。
In the heat treatment step, it is also a preferred embodiment of the present invention to perform relaxation of 0.1 to 30% in the transverse and/or longitudinal directions in the highest temperature zone of the heat treatment and/or in the cleaning zone at the exit of the heat treatment. be. Particularly in the transverse method, it is preferred to carry out a relaxation of 5 to 30%. Further, in the heat treatment step, a two-stage heat treatment may be performed.

また、高強度のために、縦方向または横方向に再延伸す
ることも好ましい。
It is also preferable to re-stretch in the machine or transverse direction for high strength.

上記延伸工程中または延伸後に、フィルムに表面光沢性
、接着性、帯電防止性、滑り性、離型性等を付与するた
めに、フィルムの片面または両面に塗布層を形成したり
、コロナ放電処理等を施したりしても構わない。特に、
フィルムに表面光沢性を付与するためにフィルム表面に
塗布層を形成することは好ましい態様である。フィルム
に表面光沢性を付与するために、塗布層を形成する場合
、塗布層中に有機、無機等の微粒子、例えば、酸化ケイ
素微粒子等を含有させることが好ましい。塗布層中に含
まれる微粒子の含有量は、好ましくは5、0〜50iv
t%、さらに好ましくは10〜40wt%、特に好まし
くは10〜30−t%の範囲であり、その平均粒径は、
好ましくは塗布層厚みの0゜1〜3.0倍、さらに好ま
しくは塗布層厚みの0.5〜2.0倍の範囲である。
During or after the above stretching process, a coating layer may be formed on one or both sides of the film, or a corona discharge treatment may be applied to give the film surface gloss, adhesiveness, antistatic properties, slipperiness, mold releasability, etc. etc. may be applied. especially,
A preferred embodiment is to form a coating layer on the surface of the film in order to impart surface gloss to the film. When forming a coating layer in order to impart surface gloss to the film, it is preferable to include organic, inorganic, etc. fine particles, such as silicon oxide fine particles, in the coating layer. The content of fine particles contained in the coating layer is preferably 5.0 to 50 iv.
t%, more preferably 10-40 wt%, particularly preferably 10-30-t%, and the average particle size is
It is preferably in the range of 0.1 to 3.0 times the thickness of the coating layer, more preferably 0.5 to 2.0 times the thickness of the coating layer.

また、延伸工程中または延伸後に形成する塗布層が、二
種以上の機能、例えば表面光沢性と離型性を兼ね備えて
いてもよく、また、二層以上の多層塗布層であってもよ
い。
Further, the coating layer formed during or after the stretching process may have two or more functions, such as surface gloss and mold release properties, or may be a multilayer coating layer of two or more layers.

〔実施例〕〔Example〕

以下、実施例にて本発明をさらに具体的に説明するが、
本発明はその要旨を越えない限り、これらの実施例に限
定されるものではない。
Hereinafter, the present invention will be explained in more detail with reference to Examples.
The present invention is not limited to these examples unless it goes beyond the gist thereof.

なお、フィルムの評価方法を以下に示す。In addition, the evaluation method of the film is shown below.

(1)  フィルムの光沢度0s(60°)日本電色工
業■製VGS−1001DP型光型光針を用いて、60
度鏡面光沢度Gs(60’)をJIS  Z  874
1に準じて測定した。すなわち、入射角、反射角60度
における黒色標準板の反射率を基準に試料の反射率を求
め光沢度とした。
(1) Glossiness of film 0s (60°)
Degree specular gloss Gs (60') JIS Z 874
Measured according to 1. That is, the reflectance of the sample was determined based on the reflectance of a black standard plate at an incident angle and a reflection angle of 60 degrees, and was defined as the glossiness.

(2)  フィルム厚み フィルム断面の写真から測定した。(2) Film thickness It was measured from a photograph of a cross section of the film.

(3)破断強度 ■インテスコ製引張試験機インテスコモデル2001型
を用いて、温度23℃、湿度50%RHに調節された室
内において、長さ50m、幅15寵の試料フィルムを、
200■/ m i nの速度で引張り、下記式に従い
次の各個を求めた。
(3) Breaking strength■ Using a tensile tester manufactured by Intesco Model 2001, a sample film with a length of 50 m and a width of 15 cm was tested in a room controlled at a temperature of 23°C and a humidity of 50% RH.
It was pulled at a speed of 200 mm/min, and the following values were determined according to the following formulas.

引張破断強度 σ=F/A 実施例1 平均粒径2.4μmの無定形シリカ粒子を0.05重量
%含有するポリエチレンテレフタレートを原料(A、)
とし、該粒子を2.7重量%含有するポリエチレンテレ
フタレートを原料(B、)とした。
Tensile breaking strength σ=F/A Example 1 Polyethylene terephthalate containing 0.05% by weight of amorphous silica particles with an average particle size of 2.4 μm was used as a raw material (A,)
Polyethylene terephthalate containing 2.7% by weight of the particles was used as a raw material (B,).

上記原料(A1)と原料(B1)とをそれぞれ別々に常
法により乾燥した後、別個の溶融押出機により、原料(
B、)を外層、原料(AI )を内層とし、厚み比Bl
 /AI /Bl =1.25/22゜5/1.25で
3層複合化させて無定形シートを製造した。
After drying the raw material (A1) and raw material (B1) separately by a conventional method, the raw material (A1) and the raw material (B1) are dried separately using a separate melt extruder.
B,) is the outer layer, the raw material (AI) is the inner layer, and the thickness ratio Bl
An amorphous sheet was produced by forming a three-layer composite with /AI /Bl =1.25/22°5/1.25.

このシートを縦方向に85℃で3.6倍延伸した後、横
方向に95℃で4.0倍延伸して、230℃で熱固定を
行い、平均厚さ25μmのフィルムを得た。
This sheet was stretched 3.6 times in the machine direction at 85°C, then 4.0 times in the transverse direction at 95°C, and heat-set at 230°C to obtain a film with an average thickness of 25 μm.

実施例2 実施例1の原料(A、)と原料(B+)を重量比で35
:65の割合でブレンドしたポリエチレンテレフタレー
トを原料(C)とした。
Example 2 The weight ratio of the raw material (A,) and raw material (B+) of Example 1 was 35
: Polyethylene terephthalate blended at a ratio of 65 was used as the raw material (C).

原料(C)と原料(A1)をそれぞれ別々に常法により
乾燥した後、別個の押出機により、原料(C)と原料(
A、)を厚み比C/AI =5/20で2層複合化させ
て、無定形シートを製造した。
After drying raw material (C) and raw material (A1) separately by a conventional method, raw material (C) and raw material (
A,) was composited into two layers with a thickness ratio of C/AI = 5/20 to produce an amorphous sheet.

このシートを用い、縦延伸倍率を3.8倍に変更する以
外は実施例1と全く同様に延伸製膜を行い、平均厚さ2
5μmのフィルムを得た。
Using this sheet, stretching film formation was carried out in exactly the same manner as in Example 1 except that the longitudinal stretching ratio was changed to 3.8 times, and the average thickness was 2.
A 5 μm film was obtained.

比較例1 実施例1の原料(A、)を常法により乾燥した後、押出
機を用いて単層にて押出し、急冷固化して無定形シート
を得た。得られたシートを実施例2と全く同様に延伸製
膜を行い、平均厚さ25μlのフィルムを得た。
Comparative Example 1 The raw material (A,) of Example 1 was dried in a conventional manner, then extruded in a single layer using an extruder, and rapidly solidified to obtain an amorphous sheet. The obtained sheet was stretched and film-formed in exactly the same manner as in Example 2 to obtain a film with an average thickness of 25 μl.

以上、得られた結果をまとめて下記表−1に示す。The results obtained above are summarized in Table 1 below.

〔発明の効果〕〔Effect of the invention〕

本発明のフィルムは、優れた艶消し効果を有し、かつ強
靭性に優れており、高強度が要求される用途、例えば転
写箔用等のベースフィルムとして、好適であり、その工
業的価値は高い。
The film of the present invention has an excellent matte effect and excellent toughness, and is suitable for applications requiring high strength, such as a base film for transfer foil, and its industrial value is expensive.

出 願 人 ダイアホイル株式会社 代 理 人Out wish Man Diafoil Co., Ltd. teenager Reason Man

Claims (1)

【特許請求の範囲】[Claims] (1)共押出により2層以上積層した複合フィルムであ
って、フィルムの片面(A面)の光沢度Gs(60゜)
が10〜90%であり、A面を構成する層のフィルム全
体に対する厚み比が0.4以下であり、かつフィルムの
縦方向および横方向の破断強度の和が36kg/mm^
2以上であることを特徴とする艶消しポリエステルフィ
ルム。
(1) A composite film in which two or more layers are laminated by coextrusion, and the glossiness of one side (side A) of the film is Gs (60°)
is 10 to 90%, the thickness ratio of the layer constituting side A to the entire film is 0.4 or less, and the sum of the breaking strength in the longitudinal and transverse directions of the film is 36 kg/mm^
A matte polyester film characterized in that the polyester film is 2 or more.
JP2228953A 1990-08-30 1990-08-30 Mat polyester film Pending JPH04110148A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2228953A JPH04110148A (en) 1990-08-30 1990-08-30 Mat polyester film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2228953A JPH04110148A (en) 1990-08-30 1990-08-30 Mat polyester film

Publications (1)

Publication Number Publication Date
JPH04110148A true JPH04110148A (en) 1992-04-10

Family

ID=16884447

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2228953A Pending JPH04110148A (en) 1990-08-30 1990-08-30 Mat polyester film

Country Status (1)

Country Link
JP (1) JPH04110148A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001062496A3 (en) * 2000-02-22 2002-04-18 Du Pont Multi-layer polymeric film and the use thereof
US7044396B2 (en) 2000-02-22 2006-05-16 Dupont Teijin Films Us Limited Partnership Multi-layer polymeric film and the use thereof
JP2015066805A (en) * 2013-09-30 2015-04-13 東レ株式会社 Biaxially orientated polyester film for mold release
CN113165355A (en) * 2018-12-06 2021-07-23 美国杜邦泰津胶片合伙人有限公司 Polymer film and use thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001062496A3 (en) * 2000-02-22 2002-04-18 Du Pont Multi-layer polymeric film and the use thereof
US7044396B2 (en) 2000-02-22 2006-05-16 Dupont Teijin Films Us Limited Partnership Multi-layer polymeric film and the use thereof
JP2015066805A (en) * 2013-09-30 2015-04-13 東レ株式会社 Biaxially orientated polyester film for mold release
CN113165355A (en) * 2018-12-06 2021-07-23 美国杜邦泰津胶片合伙人有限公司 Polymer film and use thereof
CN113165355B (en) * 2018-12-06 2023-12-05 杜邦帝人薄膜美国有限合伙 Polymer film and use thereof

Similar Documents

Publication Publication Date Title
US6991837B2 (en) Polyester film having improved oxygen barrier, comprising poly(m-xyleneadipamide) and a barrier coating, process for its production and its use
KR100285398B1 (en) Polymer sheet
JP2003520148A (en) Thermoformable UV resistant co-extruded matte polyester film, its use and method of manufacture
JP2004224050A (en) Polyester film and its manufacturing method
JP4178742B2 (en) Thermoplastic composition and film comprising the same
JP2000127323A (en) Biaxially oriented co-extruded laminate polyester film, its manufacture and its use
JP2003520149A (en) Flame-retardant co-extruded matte polyester film, its use and its production
JP2001294735A (en) Opaque-white biaxially oriented polyester film
JP2004224047A (en) Transparent, biaxially oriented, coextruded polyester film and its manufacturing method
US20050074599A1 (en) Coextruded, hot-sealable and peelable polyester film, process for its production and its use
JP2004042642A (en) Biaxially oriented coextruded laminated polyester film with sealing properties and transparency and method for manufacturing the film
JP2003532562A (en) Biaxially stretched white film, production method thereof and use thereof
KR20040091576A (en) Coextruded, Heatsealable and Peelable Polyester Film, Process for its Production and its Use
JP2004224049A (en) Polyester film and its manufacturing method
US7223459B2 (en) Coextruded, hot-sealable and peelable polyester film, process for its production and its use
JP3038843B2 (en) Matte laminated polyester film for molding
JP2014024341A (en) Polyester film for in-mold transfer
US7087312B2 (en) Polyester film having improved oxygen barrier and poly(m-xyleneadipamide)-containing overlayer, process for its production and its use
US20050287381A1 (en) Polyester film comprising poly(-xyleneadipamide)
JP2004500259A (en) UV resistant co-extruded matte polyester film, its use and method for its production
JP2006007779A (en) Biaxially stretched polyester film and its production method
JP4751511B2 (en) Polyester film with low pigment content and method for producing the same
JP2007160933A (en) Matt laminated sealing film of biaxially oriented polyester and its manufacturing process
JPH04110148A (en) Mat polyester film
JP2002331620A (en) Transparent biaxially stretched laminated polyester film and its manufacturing method