JPS5818934B2 - Polyethylene terephthalate film for vapor deposition - Google Patents

Polyethylene terephthalate film for vapor deposition

Info

Publication number
JPS5818934B2
JPS5818934B2 JP50087934A JP8793475A JPS5818934B2 JP S5818934 B2 JPS5818934 B2 JP S5818934B2 JP 50087934 A JP50087934 A JP 50087934A JP 8793475 A JP8793475 A JP 8793475A JP S5818934 B2 JPS5818934 B2 JP S5818934B2
Authority
JP
Japan
Prior art keywords
film
polyethylene terephthalate
terephthalate film
average particle
kaolin
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.)
Expired
Application number
JP50087934A
Other languages
Japanese (ja)
Other versions
JPS5214675A (en
Inventor
正路 渡辺
拓夫 中原
征二 坂本
邦男 備前
彰毎 矢野
雄三 大谷
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei Corp
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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to JP50087934A priority Critical patent/JPS5818934B2/en
Publication of JPS5214675A publication Critical patent/JPS5214675A/en
Publication of JPS5818934B2 publication Critical patent/JPS5818934B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は蒸着用ポリエチレンテレフタレートフィルムに
関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polyethylene terephthalate film for deposition.

詳しくは本発明はアルミニウム等の金属を、蒸着するこ
とによって金銀系及び転写マーク等の用途に適した優れ
た特性を有する蒸着フィルムを与えるポリエチレンテレ
フタレートフィルムに関するものである。
More specifically, the present invention relates to a polyethylene terephthalate film which, by vapor-depositing a metal such as aluminum, provides a vapor-deposited film having excellent properties suitable for applications such as gold-silver systems and transfer marks.

ポリエチレンテレフタレートフィルムから金銀系を製造
するには、二軸延伸したポリエチレンテレフタレートフ
ィルムの片面に真空下で金属、例えばアルミニウム又は
銀を蒸着し、更にエポキシ系、ポリウレタン系等の樹脂
により白色コーティングを施こした後、これを細片に切
断し、織機で織り上げる工程が一般に採用されている。
To produce a gold-silver based film from a polyethylene terephthalate film, a metal such as aluminum or silver is deposited under vacuum on one side of a biaxially stretched polyethylene terephthalate film, and then a white coating is applied with an epoxy-based, polyurethane-based, or other resin. After that, the process of cutting it into strips and weaving them on a loom is generally adopted.

又、転写マーク用フィルムは、二軸延伸したポリエチレ
ンテレフタレートフィルムに離型剤を塗布し、次いで真
空下で金属を蒸着し更に接着剤を塗布して積層体を形成
させたものであり、この積層体の接着剤側を被写体に重
ね、フィルム側から加熱したスタンプを押しつげること
によってスタンプの凸部に接する金属蒸着膜部分を、被
写体に移行させればスタンプに刻まれた金色や銀色の模
様が転写される。
The transfer mark film is made by applying a release agent to a biaxially stretched polyethylene terephthalate film, then depositing metal under vacuum, and then applying an adhesive to form a laminate. By placing the adhesive side of the body on the subject and pressing the heated stamp from the film side, the metal vapor deposited film that touches the convex part of the stamp is transferred to the subject, and the gold or silver pattern engraved on the stamp can be seen. transcribed.

ポリエチレンテレフタレートフィルムは透明性、機械的
性質、耐薬品性等が優れており、多くの用途を有してい
るが、滑り性に問題があり、そのため巻き上げ等の作業
性に欠ける点がある。
Polyethylene terephthalate film has excellent transparency, mechanical properties, chemical resistance, etc., and has many uses, but it has a problem with slipperiness, and therefore lacks workability such as winding.

滑り性を改良する方法としては、種々の不活性物質、例
えばシリカ、カオリン、タルク、アルミナ、アミノ珪酸
塩、ケイソウ士、陶土等な添加し表面を粗くする方法が
知られている。
As a method for improving the slipperiness, it is known to roughen the surface by adding various inert substances such as silica, kaolin, talc, alumina, aminosilicates, diatomite, china clay, etc.

ところが、これら不活性物質を従来の方法に従って添加
すると滑り性は改善されるものの、逆に透明性が低下し
たり、表面に凹凸が生成する不都合を生ずる。
However, when these inert substances are added according to conventional methods, although the slipperiness is improved, there are disadvantages such as a decrease in transparency and the formation of irregularities on the surface.

その上、本発明者らの知見によれば、このようなフィル
ムに金属を蒸着させた場合には、フィルムを巻取る際、
金属面とフィルム面との接触によりしばしば金属面に機
械方向に無数の傷(顕微鏡によると傷の入っている部分
は金属が剥ぎ取られてしまったことが観察される。
Moreover, according to the findings of the present inventors, when metal is vapor-deposited on such a film, when the film is wound,
Contact between the metal surface and the film surface often causes numerous scratches on the metal surface in the machine direction (according to a microscope, it is observed that the metal has been peeled off from the scratched areas).

)が見られ、そのために最終製品の価値を著しく損う。), which significantly reduces the value of the final product.

本発明者らはこの点に鑑み種々検討を重ねた結果、特定
粒径のカオリンを特定量添加して得たポリエチレンテレ
フタレートフィルムは金属を蒸着させて積層体としたと
きに、金属側とフィルム側の光沢に差がなく、巻取工程
において金属面に傷が入りにくくかつ作業性が良好であ
ることを見い出し本発明を完成した。
The inventors of the present invention have conducted various studies in view of this point, and have found that when a polyethylene terephthalate film obtained by adding a specific amount of kaolin with a specific particle size is made into a laminate by vapor-depositing metal, the metal side and the film side The present invention was completed by discovering that there is no difference in gloss, that the metal surface is less likely to be scratched during the winding process, and that workability is good.

すなわち、本発明は、平均粒径0.2〜3.0μのカオ
リンを200〜3000 ppm添加してなり、且つ、
平均粒径(μ)と添加量(ppm)との積が300〜1
500であることを特徴とする蒸着用ポリエチレンテレ
フタレートに存する。
That is, in the present invention, 200 to 3000 ppm of kaolin with an average particle size of 0.2 to 3.0 μm is added, and
The product of the average particle size (μ) and the amount added (ppm) is 300 to 1
The polyethylene terephthalate for vapor deposition is characterized by having a

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

本発明におけるポリエチレンテレフタレートとはポリエ
チレンテレフタレート単独のもの及びポリエチレンテレ
フタレート特性を損わない程度に共重合成分を存在させ
たもの及び他のポリマーとのブレンド物を指し、具体的
にはエチレンテレフタレート単位を70モル%以上含む
ポリエステルである。
In the present invention, polyethylene terephthalate refers to polyethylene terephthalate alone, polyethylene terephthalate in which a copolymer component is present to an extent that does not impair the properties, and a blend with other polymers. Specifically, polyethylene terephthalate units include 70 It is a polyester containing mol% or more.

本発明のポリエチレンテレフタレートフィルムを製造す
るには、常法により粉砕、分級したカオリンの微粒子を
本発明の特定な条件を満足するようにポリエチレンテレ
フタレートを主体とする重合体に添加し、重合体を次い
でシート状に溶融押出しした後、縦及び横方向に3倍以
上に二軸延伸し該微粒子をフィルム表面に分散させる。
In order to produce the polyethylene terephthalate film of the present invention, fine particles of kaolin that have been crushed and classified by a conventional method are added to a polymer mainly composed of polyethylene terephthalate so as to satisfy the specific conditions of the present invention, and then the polymer is After melt-extruding into a sheet, the fine particles are dispersed on the surface of the film by biaxially stretching the film by a factor of 3 or more in the longitudinal and transverse directions.

該微粒子の添加方法としてはエチレングリコールにスラ
リー状として分散させたものを重合工程において添加す
るのが最も好ましいが重合を終了した後成型前に粉末状
で添加し、押出機中で分散させてもよい。
The most preferable method for adding the fine particles is to disperse them in the form of a slurry in ethylene glycol and add them during the polymerization process, but they can also be added in the form of powder after polymerization and before molding, and dispersed in an extruder. good.

カオリン微粒子の添加に当っては粒径および添加量が、
本発明の特定な条件を満足することが肝要である。
When adding kaolin fine particles, the particle size and amount added are
It is essential that the specific conditions of the invention are met.

すなわち、粒径については作業性や表裏の差、フィルム
の美観等の観点から制限があり、(後述する測定法で測
定した)平均粒径が0.2〜3.0μ、好ましくは0.
2〜2.0μでなければならない。
That is, there are restrictions on the particle size from the viewpoint of workability, the difference between the front and back sides, the aesthetic appearance of the film, etc., and the average particle size (measured by the measuring method described later) is 0.2 to 3.0 μm, preferably 0.2 μm to 3.0 μm.
Must be 2-2.0μ.

平均粒径0.2μ未満の粒子を用いると摩擦係数を含め
た作業性が充分ではない。
If particles with an average particle diameter of less than 0.2 μm are used, workability including friction coefficient will not be sufficient.

一方平均粒径が3μより大きな粒子を用いると表裏の差
が悪くなるのは勿論のことフィルム表面に形成された凹
凸が肉眼で見えるようになりフィルムの美観が損われて
好ましくない。
On the other hand, if particles having an average particle diameter of more than 3 μm are used, not only the difference between the front and back surfaces becomes poor, but also the unevenness formed on the film surface becomes visible to the naked eye, which impairs the aesthetic appearance of the film, which is undesirable.

添加量は、透明性、作業性、フィルターライフ等の観点
から200〜3000 ppm、好ましくは500〜2
000 ppmの範囲が適当である。
The amount added is 200 to 3,000 ppm, preferably 500 to 2,000 ppm from the viewpoint of transparency, workability, filter life, etc.
A range of 0.000 ppm is suitable.

添加量が200 ppm未満であるとスリット時の巻磁
の発生を防ぐことができず、一方、3000 可屈を越
えるとフィルターライフの点で問題が生じ、生産効率が
下がると共に蒸着フィルムにしたとき傷が生じやすくな
る。
If the amount added is less than 200 ppm, it will not be possible to prevent the occurrence of magnetic winding during slitting, while if it exceeds 3000 ppm, problems will occur in terms of filter life, production efficiency will decrease, and when made into a vapor deposited film. Scratches are more likely to occur.

更に、平均粒径(μ)及び添加量(PPm )の積を金
属面への傷つきにくさ、表裏の差、摩擦係数等を満足さ
せるために300〜1500に保つ要がある。
Further, the product of the average particle diameter (μ) and the amount added (PPm) must be kept at 300 to 1500 in order to satisfy the requirements such as resistance to damage to metal surfaces, difference between the front and back surfaces, and coefficient of friction.

この積が300より小さいと摩擦係数が太き(なり、1
500より大きいと表裏の差が著しくなり、また傷が入
りやすくなる。
If this product is smaller than 300, the friction coefficient becomes thick (becomes 1
If it is larger than 500, the difference between the front and back will be significant and scratches will occur easily.

なお、ここで傷の入りに(さを判定する目安として、後
述の傷の測定法に従って測定したT1及びT2が各々2
.0%以下及び2.5%以下であればよい。
In addition, here, as a guideline for determining the extent of scratches, T1 and T2 measured according to the scratch measurement method described below are each 2.
.. It is sufficient if it is 0% or less and 2.5% or less.

T1及びT2が大きくなると金属面上の傷が肉眼で見え
るようになり最終加工品の品質を低下させる。
When T1 and T2 become large, scratches on the metal surface become visible to the naked eye, degrading the quality of the final processed product.

本発明のポリエチレンテレフタレートフィルムは、上述
したように作業性が良好で、表裏の差が少なく、蒸着し
た金属面に傷がつきにくい等の優れた特性を有しており
、金銀系及び転写マーク等の用途に好適である。
As mentioned above, the polyethylene terephthalate film of the present invention has excellent properties such as good workability, little difference between the front and back sides, and resistance to scratches on the metal surface on which it is vapor-deposited. Suitable for applications such as

次に実施例を用いて本発明をさらに具体的に説明する。Next, the present invention will be explained in more detail using Examples.

なお試験方法は下記に従った。粒子の平均粒径: 顕微鏡法を用いた。The test method was as follows. Average particle size of particles: using microscopy.

延伸したフィルムについて反射法で写真撮影を行ない最
大径を測定した。
The stretched film was photographed using a reflection method and the maximum diameter was measured.

この値を用いて重量等制球換算を行ない積弊重量分率5
0%の時の値を平均粒径とした。
Using this value, perform weight control conversion and obtain a cumulative weight fraction of 5.
The value at 0% was taken as the average particle size.

摩擦係数: ASTM1894−63に準じテープ状のサンプルで測
定できる様改良したものでサンプルとして巾15mm長
さ150龍のものを用い測定スピードは20 m711
/minとした。
Friction coefficient: Improved to allow measurement with a tape-shaped sample according to ASTM1894-63.The sample was 15 mm wide and 150 mm long, and the measurement speed was 20 m711.
/min.

フイルムヘーズ; ASTM D1003−59Tに示された方法に準じ
日本重色製濁度計NDH−2A型を用い測定を行なった
Film haze: Measurement was carried out using a turbidity meter NDH-2A manufactured by Nippon Heavy Industries in accordance with the method shown in ASTM D1003-59T.

傷; アルミ蒸着(厚さ500人)フィルムのA1面の上にサ
ンプルのフィルムを重ね一定荷重をかけたのち20 a
mlamの速度でAI蒸着フィルムを滑らせる。
Scratch: After placing the sample film on the A1 side of the aluminum vapor-deposited (500mm thick) film and applying a constant load, 20a
Slide the AI-deposited film at a speed of mlam.

その後AI蒸着フィルムを取り出しその全透過率Tを日
本重色製濁度計NDH−2A型で測定した。
Thereafter, the AI-deposited film was taken out and its total transmittance T was measured using a turbidity meter NDH-2A manufactured by Nippon Heavy Industries.

荷重30 ft /crAの時の全透過率をT1とし8
0fi/cmの時の値をT2とした。
The total transmittance when the load is 30 ft/crA is T1, and 8
The value at 0fi/cm was defined as T2.

(傷がつかなければT1、T2ともに0となる。(If there is no scratch, both T1 and T2 will be 0.

)表裏の差; 2枚のサンプルを同時に並べて真空蒸着器に入れAIを
蒸着したのち1枚はポリエチレンテレフタレート面もう
1枚はA1面を上にして並べ目視で判定した。
) Difference between front and back; Two samples were lined up at the same time and placed in a vacuum evaporator to deposit AI, and then one was placed with the polyethylene terephthalate side facing up, and the other with the A1 side facing up, and visually judged.

良い方から順にA、B、C及びDの4ランクに分け8以
上を合格とした。
The scores were divided into four ranks, A, B, C, and D, in descending order of quality, and scores of 8 or higher were considered to be passing.

実施例 1 ジメチルテレフタレート100部、エチレングリコール
75部及び酢酸マンガン75部をエステル交換槽に仕込
み徐々に昇温してエステル交換反応を行ない生成するメ
タノール及び過剰のエチレングリコールを留出させた。
Example 1 100 parts of dimethyl terephthalate, 75 parts of ethylene glycol and 75 parts of manganese acetate were charged into a transesterification tank, and the temperature was gradually raised to carry out the transesterification reaction, and the resulting methanol and excess ethylene glycol were distilled off.

次いで反応混合物に三酸化アンチモン0.03部及び平
均粒径0.2μのカオリン(米国エンゲルノ・ルト社製
、ASPを分級したもの)のエチレングリコールスラリ
ーを添加量が重合後のポリマーに対し2000 ppm
となる様に加え更に亜リン酸0.03部を加えたのち0
、5mmHgの減圧下280℃で4時間重合綿合反応を
行なった。
Next, an ethylene glycol slurry of 0.03 parts of antimony trioxide and kaolin (manufactured by Engelnord, USA, classified from ASP) with an average particle size of 0.2 μm was added to the reaction mixture in an amount of 2000 ppm based on the polymerized polymer.
In addition, add 0.03 part of phosphorous acid so that it becomes 0.
A polymerization reaction was carried out at 280° C. for 4 hours under a reduced pressure of 5 mmHg.

このようにして得られたポリマーをダイスよりシート状
に押出しガラス転移点以上の温度で縦及び横方向に夫々
3.5倍ずつ延伸を行なった後厚さ12μのフィルムと
した。
The thus obtained polymer was extruded into a sheet through a die and stretched by 3.5 times in both the longitudinal and transverse directions at a temperature above the glass transition point to form a film with a thickness of 12 μm.

得られたフィルムについて摩擦係数、表裏の差及びAI
蒸着面への傷のつきやすさ烈1j定した。
The friction coefficient, difference between the front and back sides, and AI of the obtained film
The ease with which the vapor-deposited surface was scratched was determined.

結果な第1表に示す。The results are shown in Table 1.

実施例2〜10及び比較例1〜7 実施例1においてカオリンとしてASPを分級した平均
粒径の異なるものを所定量添加した以外は実施例1の方
法と同様にしてフィルムを製造した。
Examples 2 to 10 and Comparative Examples 1 to 7 Films were produced in the same manner as in Example 1, except that a predetermined amount of kaolin classified as ASP with different average particle diameters was added.

物性の測定結果を第1表に併記する。実施例11.12
及び比較例 8 実施例1において、カオリンとして、米国ティーレ・カ
オリン・カンパニー社製カオプライトを分級した平均粒
径1μのカオリンを用い添加を変えた以外は実施例1の
方法と同様にしてフィルムを製造し′た。
The measurement results of physical properties are also listed in Table 1. Example 11.12
Comparative Example 8 A film was produced in the same manner as in Example 1, except that the kaolin used was kaolin with an average particle size of 1 μm, which was obtained by classifying kaoprite manufactured by Thiele Kaolin Company, Inc. in the United States, and the addition was changed. did.

物性の測定結果を第1表に併記する。比較例 9〜13 実施例1において添加したカオリンの代りにタルク(林
化成製、ミクロンホワイト)、水酸化アルミニウム(昭
和電工製、ハイジライ)、H−41)、シリカ(富士デ
ビイソン化学製、サイクロイド266)及びa−アルミ
ナ(不二見研摩剤工業製、WA−8000)を分級し、
第1表に示した粒径のものを所定量用いた以外は実施例
1の方法に準じてフィルムを製造した。
The measurement results of physical properties are also listed in Table 1. Comparative Examples 9 to 13 Instead of kaolin added in Example 1, talc (Hayashi Kasei, Micron White), aluminum hydroxide (Showa Denko, Heijirai, H-41), silica (Fuji Davison Chemical, Cycloid 266) ) and a-alumina (manufactured by Fujimi Abrasive Industries, WA-8000),
A film was produced in accordance with the method of Example 1, except that a predetermined amount of particles having the particle sizes shown in Table 1 was used.

物性の測定結果を第1表に併記する。The measurement results of physical properties are also listed in Table 1.

Claims (1)

【特許請求の範囲】[Claims] 1 平均粒径0.2〜3−0μのカオリンを200〜3
000 ppm添加してなり、且つ、平均粒径(μ)と
添加量(ppm)との積が300〜】500であること
を特徴とする蒸着用ポリエチレンテレフタレートフィル
ム。
1 Kaolin with an average particle size of 0.2 to 3-0μ is 200 to 3
A polyethylene terephthalate film for vapor deposition, characterized in that the product of the average particle diameter (μ) and the amount added (ppm) is from 300 to 500.
JP50087934A 1975-07-18 1975-07-18 Polyethylene terephthalate film for vapor deposition Expired JPS5818934B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50087934A JPS5818934B2 (en) 1975-07-18 1975-07-18 Polyethylene terephthalate film for vapor deposition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50087934A JPS5818934B2 (en) 1975-07-18 1975-07-18 Polyethylene terephthalate film for vapor deposition

Publications (2)

Publication Number Publication Date
JPS5214675A JPS5214675A (en) 1977-02-03
JPS5818934B2 true JPS5818934B2 (en) 1983-04-15

Family

ID=13928724

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50087934A Expired JPS5818934B2 (en) 1975-07-18 1975-07-18 Polyethylene terephthalate film for vapor deposition

Country Status (1)

Country Link
JP (1) JPS5818934B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0343218Y2 (en) * 1985-07-05 1991-09-10

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5435470U (en) * 1977-08-13 1979-03-08
JPS5467114U (en) * 1977-10-19 1979-05-12
JPS5818935B2 (en) * 1978-07-07 1983-04-15 ダイアホイル株式会社 Polyester film for vapor deposition
JPS56166059A (en) * 1980-05-27 1981-12-19 Teijin Ltd Stamping-wheel
JPS5872444A (en) * 1981-10-27 1983-04-30 帝人株式会社 Evaporated film
US4489110A (en) * 1982-01-15 1984-12-18 Bayer Aktiengesellschaft Polyethylene terephthalate moulding compositions having high reflectivity

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5024348A (en) * 1973-07-04 1975-03-15

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5024348A (en) * 1973-07-04 1975-03-15

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0343218Y2 (en) * 1985-07-05 1991-09-10

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JPS5214675A (en) 1977-02-03

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