JPS595101B2 - Easy-slip film - Google Patents

Easy-slip film

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Publication number
JPS595101B2
JPS595101B2 JP53108887A JP10888778A JPS595101B2 JP S595101 B2 JPS595101 B2 JP S595101B2 JP 53108887 A JP53108887 A JP 53108887A JP 10888778 A JP10888778 A JP 10888778A JP S595101 B2 JPS595101 B2 JP S595101B2
Authority
JP
Japan
Prior art keywords
film
coefficient
friction
polymer
surface roughness
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
JP53108887A
Other languages
Japanese (ja)
Other versions
JPS5534968A (en
Inventor
敏之 朝倉
弘明 小林
幸男 野口
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP53108887A priority Critical patent/JPS595101B2/en
Publication of JPS5534968A publication Critical patent/JPS5534968A/en
Publication of JPS595101B2 publication Critical patent/JPS595101B2/en
Expired legal-status Critical Current

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  • Laminated Bodies (AREA)
  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
  • Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
  • Organic Insulating Materials (AREA)

Description

【発明の詳細な説明】 本発明は表面粗度を一定の範囲内にししかも摩擦係数を
小さくした二軸配向のポリーp−フェニレンスルフィド
フィルムに関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a biaxially oriented poly p-phenylene sulfide film whose surface roughness is within a certain range and whose coefficient of friction is reduced.

従来より産業用フィルム素材としてポリエチレンテレフ
タレートフィルムやポリプロピレンフィルム、ポリイミ
ドフィルムなどが広く使用されているが溶融製膜できし
かも耐熱性、種々の特性、コストなどにバランスのとれ
た高級フィルムはいまだに決定的なものがなく各所で検
討がなされている。我々は素材にポリーp−フェニレン
スルフィドを選びこのポリマを使用して高級フィルムを
作製することを検討していたが実用的なフィルムとする
ためには、表面の粗度を調整し、フィルムの摩擦係数を
一定以下にしておけば取扱いや各種機器用素材として非
常にすぐれたフィルムとなわ5 得ることを見い出し本
発明に到達した。すなわち本発明は、フィルム同志の動
摩擦係数が20℃、相対湿度70%の下で0.75以下
でありかつフィルム表面粗度が0.90μ/ 5nml
以下であることを特徴とする二軸配向の実質的にポリー
10p−フェニレンスルフィドから成るフィルムに関す
るものである。本発明のポリー p−フェニレンスルフ
ィドはその90%モル以上が構成単位丹。
Conventionally, polyethylene terephthalate film, polypropylene film, polyimide film, etc. have been widely used as industrial film materials, but high-quality films that can be melt-formed and are well-balanced in terms of heat resistance, various properties, cost, etc. are still the definitive film. There is no such thing, and consideration is being made in various places. We selected poly p-phenylene sulfide as the material and were considering using this polymer to create a high-grade film, but in order to make it a practical film, we needed to adjust the surface roughness and reduce the friction of the film. We have discovered that if the coefficient is kept below a certain level, we can obtain films and ropes that are excellent in handling and as materials for various types of equipment, and have thus arrived at the present invention. That is, the present invention provides a film in which the coefficient of dynamic friction between films is 0.75 or less at 20°C and 70% relative humidity, and the surface roughness of the film is 0.90μ/5nml.
The present invention relates to a film consisting essentially of biaxially oriented poly-10p-phenylene sulfide, characterized in that: More than 90% mole of the poly p-phenylene sulfide of the present invention is a structural unit of red.

5−)− か15ら成るポリマであることが好ましく、
90モル%より少ないと結晶性が低下し二軸延伸結晶化
が困難であわ、耐熱性、機械的物性などに満足のいくも
のは得られ難い。
5-)- is preferably a polymer consisting of
If it is less than 90 mol%, crystallinity decreases and biaxial stretching crystallization becomes difficult, making it difficult to obtain satisfactory heat resistance, mechanical properties, etc.

なお該ポリマの構成単位のうち10モル%未満であれば
他の共重合単位を含ん20でいてもさしつかえない。か
かる共重合単位としては、例えば3官能単位(例:夛s
−)、エーテル単位(例:00吾s一)、ス□ ルホン
単位(例:0502÷s−)、メタ結合単位(例會5−
)などが挙げられる。
It should be noted that the polymer may contain other copolymerized units as long as they account for less than 10 mol % of the constituent units of the polymer. Such copolymerized units include, for example, trifunctional units (e.g.
-), ether unit (example: 00 s -), sulfon unit (example: 0502 ÷ s -), meta-bonding unit (example 5-
), etc.

また重合したポリマを加熱することによつて、30わず
かながらの橋かけを起こさせることも可能である。かか
る構成単位から成るポリーp−フェニレンスルフィドの
合成法としては種々あるがp−ジハロベンゼンと硫化ア
ルカリまたは硫化アルカリ土35類金属とを極性有機溶
媒中で反応させる方法が好適であシ、重合条件としては
200〜3500Cの温度が適用され、該重合系内の圧
力ならびに重合時間は使用される触媒の種類や所望する
重合度によつて適宜決定される。
It is also possible to cause slight crosslinking by heating the polymerized polymer. Although there are various methods for synthesizing poly p-phenylene sulfide composed of such structural units, a method of reacting p-dihalobenzene with an alkali sulfide or an alkaline earth metal sulfide 35 in a polar organic solvent is suitable, and the polymerization conditions are as follows: A temperature of 200 to 3500C is applied, and the pressure within the polymerization system and the polymerization time are appropriately determined depending on the type of catalyst used and the desired degree of polymerization.

一方、製膜法は本質的に溶融製膜法でありかつ二軸延伸
、熱固定を行なうべきである。
On the other hand, the film forming method is essentially a melt film forming method, and biaxial stretching and heat setting should be performed.

すなわちほとんど非晶性のフイルムを二軸に延伸後結晶
化のための熱処理を行なう方法である。非晶性フイルム
を得るには重合体をプレス、押出し機等によりフイルム
状に賦形した後結晶化がそれほど進行しないように空気
、水、ロール等を使用して急冷する。
That is, this is a method in which a nearly amorphous film is biaxially stretched and then heat treated for crystallization. To obtain an amorphous film, a polymer is shaped into a film using a press, an extruder, etc., and then rapidly cooled using air, water, a roll, etc. so that crystallization does not progress too much.

非晶性フイルムの密度は1.3309/Cc以下である
が延伸後熱処理したフイルムは1.350以上に通常上
げられる。延伸方法としては、ポリマのガラス転移温度
付近80〜100℃の温度でロール、テンタ方式による
のが便利であるが、通常面積倍率として3倍以上さらに
好ましくは7倍以上延伸されるのが得られるフイルムの
物性から見て好ましい。このようにして二軸に延伸され
たフイルムは結晶化度を上げるため150〜2800C
好ましくは250〜280℃の範囲で十分な時間、通常
1〜120秒間緊張下に加熱される。本発明の特徴であ
る表面粗度の調整は重合程あるいは製膜工程またはその
両方で行なうことができる。
The density of an amorphous film is 1.3309/Cc or less, but the density of a film heat-treated after stretching is usually increased to 1.350 or more. As for the stretching method, it is convenient to use a roll or tenter method at a temperature of 80 to 100°C near the glass transition temperature of the polymer, but it is usually possible to obtain an area stretching ratio of 3 times or more, more preferably 7 times or more. This is preferable in terms of the physical properties of the film. The film thus biaxially stretched is heated at 150 to 2800 C to increase the crystallinity.
Preferably, it is heated under tension at a temperature in the range of 250 to 280°C for a sufficient period of time, usually for 1 to 120 seconds. Adjustment of surface roughness, which is a feature of the present invention, can be carried out during the polymerization process, the film forming process, or both.

重合時あるいは重合終了時にポリマ中に不活性無機粒子
を添加する方法、あるいは重合のために使用した不浩解
塩を一定量残存させる方法などが簡便であるが、添加す
る粒子としては例えば平均粒径20μ以下のシリカ、ア
ルミナ、炭素、ガラス、炭酸カルシウム、リン酸カルシ
ウムなどの微粉末あるいはこれらの混合物などが使用で
きる。また製膜工程あるいは後工程中にとり得る方法と
しては粗面化ロールの使用、表面を酸化処理した後の延
伸、固形物によるブラスト処理などが挙げられる。
It is convenient to add inert inorganic particles to the polymer during or after polymerization, or to leave a certain amount of the insoluble salt used for polymerization, but the particles to be added are, for example, average particles. Fine powders of silica, alumina, carbon, glass, calcium carbonate, calcium phosphate, etc. having a diameter of 20 μm or less, or mixtures thereof can be used. Methods that can be used during the film forming process or post-process include use of a roughening roll, stretching after oxidizing the surface, and blasting with a solid material.

種々のベース表面平滑用途に使用される場合にベース片
面を平滑にし裏面をもつと大きな凹凸にすることも可能
であり、これらの調整は本発明の範囲内で多層押出し、
片面のみの処理などで達成することができる。
When used for various base surface smoothing applications, it is possible to make one side of the base smooth and the other side have large irregularities, and these adjustments can be made within the scope of the present invention by multilayer extrusion,
This can be achieved by processing only one side.

また、両面とも平均0.01μ/50mのような平滑な
面であつてもコーテイングにより表面摩擦係数を調整す
ることも可能である。フイルムの表面特性は摩擦係数と
微少凹凸の程度により特徴付けられ、両者ともに小さい
ほうが種々の点で好ましい。例えば平均0.90μ/5
Dm(フイルム表面の走査長5mの平均の凹凸が0.9
0μであることを意味する)を越すような大きな凹凸に
なるど摩擦係数は小さくできるが、グラフイツク用途や
録音録画再生などの用途にフイルムを使用した際には良
好なものは得られない。また0.001μ/5m未満の
ような平滑なものは摩擦係数も大きくなり易く取扱いが
困難であるばかりでなく実際に作製も困難である。また
摩擦係数としてはフイルム同志の値として動摩擦係数で
0.75を越すとフイルムの巻取り時にしわになつたり
、折れ目が発生したジし好ましくない。ポ〃−p一フエ
ニレンスルフイドニ軸延伸フイルムの本質的な自己潤滑
性とさらに表面に微少な凹凸を付与することの組み合わ
せにより本発明のようにすぐれた表面特性を保持させる
ことができる。本発明のフイルムは写真フイルムベース
、磁気録音録画ベース、コンデンサーベースなどの精密
分野や一般電気絶縁用ベース、フレキシブル印刷回路基
板などに非常に有用なベースフイルムを与えるものであ
る。
Furthermore, even if both surfaces are smooth with an average diameter of 0.01 μ/50 m, it is possible to adjust the surface friction coefficient by coating. The surface characteristics of the film are characterized by the coefficient of friction and the degree of minute irregularities, and it is preferable from various points of view that both of them be smaller. For example, average 0.90μ/5
Dm (average unevenness of the film surface over a scanning length of 5 m is 0.9
Although the coefficient of friction can be reduced by creating large irregularities exceeding 0μ (meaning 0μ), it is not possible to obtain a good coefficient of friction when the film is used for applications such as graphics or recording and playback. Furthermore, a smooth material with a diameter of less than 0.001 μ/5 m tends to have a large coefficient of friction and is not only difficult to handle but also difficult to actually manufacture. Furthermore, if the friction coefficient exceeds 0.75 in terms of dynamic friction coefficient between the films, it is not preferable because the film may wrinkle or crease during winding. The excellent surface properties of the present invention can be maintained by combining the essential self-lubricating property of the poly-p-phenylene sulfide biaxially stretched film and the provision of minute irregularities on the surface. The film of the present invention provides a very useful base film for precision fields such as photographic film bases, magnetic recording bases, capacitor bases, general electric insulation bases, flexible printed circuit boards, and the like.

な}、フイルム表面の凹凸の測定は触針式の表面粗度計
や反射干渉あるいは微分干渉による顕微鏡測定などが好
都合であるが特に触針式表面粗度計を使用して測定する
方法が好ましい。
Although it is convenient to measure the unevenness of the film surface using a stylus-type surface roughness meter or microscopic measurement using reflection interference or differential interference, it is particularly preferable to measure using a stylus-type surface roughness meter. .

また摩擦係数の測定は金属などの鏡面にフイルムを固定
し、フイルム面同志を密着させ一定荷重下に一方側を等
速で移動させる方法によつて動摩擦係数を簡便に測定す
ることができる。
Furthermore, the coefficient of friction can be easily measured by fixing a film to a mirror surface such as metal, bringing the film surfaces into close contact with each other, and moving one side at a constant speed under a constant load.

また、本発明のフイルムは耐候剤、着色剤、酸化防止剤
などの混合や金属酸化物、他ポリマを本発明の表面特性
をそこなわない程度の範囲で含有していてもかまわない
Further, the film of the present invention may contain a mixture of weathering agents, colorants, antioxidants, etc., metal oxides, and other polymers to the extent that the surface characteristics of the present invention are not impaired.

以下本発明を実施例をもつて説明する。The present invention will be explained below with reference to Examples.

な卦実施例中表面粗度は小坂研究所作製による万能表面
形状測定器SE−3EによV)4μ径の針を使用し0.
079の荷重下に走査し10万倍で粗度を観察した。
In the examples, the surface roughness was measured using a universal surface profile measuring instrument SE-3E manufactured by Kosaka Laboratory using a needle with a diameter of 4μ.
It was scanned under a load of 0.079 and the roughness was observed at a magnification of 100,000 times.

また摩擦係数はASTMD−1894B法に準じフイル
ム/フイルム間の動摩擦係数を雰囲気温度20℃、相対
湿度70%のもとで測定した。
The coefficient of friction was determined by measuring the coefficient of dynamic friction between films according to the ASTM D-1894B method at an ambient temperature of 20° C. and a relative humidity of 70%.

実施例 1比較実施例 1硫化ナトリウム(9水塩)1
モル、水酸化ナトリウム0.15モル、酢酸リチウム0
.8モル、N一メチルピロリドン4モルの割合で501
オートクレーブに入れ200モCまで徐々に昇温し水と
Nメチルピロリドンの一部を留去した。
Examples 1 Comparative Examples 1 Sodium sulfide (nase hydrate) 1
mole, sodium hydroxide 0.15 mole, lithium acetate 0
.. 501 in the ratio of 8 mol and 4 mol of N-methylpyrrolidone.
The mixture was placed in an autoclave and the temperature was gradually raised to 200 mC to distill off water and a portion of N-methylpyrrolidone.

この系にp−ジクロルベンゼン1,02モルを添加後系
内を乾燥窒素で4kg眉に加圧し280℃にて8時間攪
拌下に重合を行なつた。内容物を熱湯で3回、アセトン
で3回、さらに熱湯で2回、アセトンで1回洗浄した後
粒状のポリマを100℃にて24時間乾燥した。別に平
均粒径約40μの炭酸カルシウムをボールミルにて12
0時間粉砕し平均粒径約2μの微粉末を得た。
After adding 1.02 moles of p-dichlorobenzene to this system, the system was pressurized to 4 kg with dry nitrogen and polymerization was carried out at 280 DEG C. for 8 hours with stirring. After washing the contents three times with hot water, three times with acetone, two times with hot water, and once with acetone, the granular polymer was dried at 100° C. for 24 hours. Separately, 12 pieces of calcium carbonate with an average particle size of about 40μ was milled in a ball mill.
The mixture was ground for 0 hours to obtain a fine powder with an average particle size of about 2 μm.

粉砕前後の炭酸カルシウムをペンシェル型ミキサー内で
先に調整したポリマに0,5%添加した後押出機により
(300〜32『C)カットに成形後チツプ化した。次
にこれらのポリマを水冷キヤステイングドラム上へキヤ
ストし350μの未延伸フイルムを得た後、ロールによ
り縦方向へ9『Cにて3.5倍延伸し、さらにテンタ方
式の延伸機により横方向へ(3.5倍延伸後定長下に電
熱ヒーターにより約2700Cにて30秒間熱固定を行
ない20μのフイルムを得た。
Calcium carbonate before and after pulverization was added in an amount of 0.5% to the previously prepared polymer in a pen shell type mixer, and then molded into cuts (300 to 32'C) using an extruder and then chipped. Next, these polymers were cast onto a water-cooled casting drum to obtain an unstretched film of 350μ, which was then stretched 3.5 times in the machine direction at 9'C with rolls, and further stretched in the transverse direction with a tenter-type stretching machine. (After stretching 3.5 times, heat setting was carried out at about 2700C for 30 seconds under constant length with an electric heater to obtain a 20μ film.

こうして得られた2種のフイルムを磁気テープにした場
合どのような差が出るのかを検討し表1の結果を得た。
なお磁気テープの作製は下記のようにして行なつた。
The results shown in Table 1 were obtained by examining what difference would occur when the two types of films thus obtained were made into magnetic tape.
The magnetic tape was manufactured as follows.

◎磁性塗料の組成 γ−Fe2O3粉末 32部カーボ
ンブラツク 2.7部ビニライト(
U.C.C.製)VAGH4.5部エスライン(グツド
リツチ社)57025.0部メチルエチルケトン
22部メチルイソブチルケトン
12.7部この磁性塗料を5μになるように塗布乾燥
後ヘリカルスキヤン型ビデオテープレコーダ(松下電器
製、NV3O2O)で表面に関係すると思われる測定を
行なつた。
◎Composition of magnetic paint γ-Fe2O3 powder 32 parts Carbon black 2.7 parts Vinyrite (
U. C. C. VAGH 4.5 parts S-line (Gutudoritsu) 57025.0 parts Methyl ethyl ketone
22 parts methyl isobutyl ketone
12.7 parts This magnetic paint was coated to a thickness of 5 μm, and after drying, measurements considered to be related to the surface were performed using a helical scan video tape recorder (NV3O2O, manufactured by Matsushita Electric).

上記のように本発明フイルムは精密分野においてもすぐ
れた表面特性を発揮することが判明した。
As mentioned above, it has been found that the film of the present invention exhibits excellent surface properties even in the precision field.

実施例 2比較実施例 2本例は極めて平滑な表面を有
するフイルムに関するものである。
Example 2 Comparative Example 2 This example relates to a film with an extremely smooth surface.

実施例1と同様にして合成し洗浄したポリマをさらに酢
酸リチウム1部、ポリマ2部、N−メチルピロリドン1
5部を混合しオートクレーブ沖で、270℃にて3時間
攪拌下に加熱後、同様に水、アセトンを洗浄を繰返した
A polymer synthesized and washed in the same manner as in Example 1 was further added with 1 part of lithium acetate, 2 parts of polymer, and 1 part of N-methylpyrrolidone.
5 parts were mixed and heated in an autoclave at 270° C. for 3 hours with stirring, and then washed with water and acetone in the same manner.

乾燥したポリマをチツブ化した後、実施例1とまつたく
同様な手法で二軸延伸熱固定し20〜25μのフイルム
を得た。このフイルムの表面中心線平均粗さは0.00
5μ/51n01と平滑であつたが、フイルム間の動摩
擦係数は0.69であり、巻取りが不可能等の困難は生
じなかつた。一方、ポリエチレンテレフタレートフイル
ムで同様な程度の表面粗度を持つたものは、1.0以上
の摩擦係数を有し、取扱いが非常に困難であつた。
After the dried polymer was formed into a chip, it was biaxially stretched and heat-set in the same manner as in Example 1 to obtain a film of 20 to 25 μm. The surface center line average roughness of this film is 0.00
Although the film was smooth with a value of 5μ/51n01, the coefficient of dynamic friction between the films was 0.69, and no difficulties such as impossibility of winding occurred. On the other hand, polyethylene terephthalate films with similar surface roughness had a coefficient of friction of 1.0 or more and were extremely difficult to handle.

Claims (1)

【特許請求の範囲】[Claims] 1 フィルム同志の動摩擦係数が20℃、相対湿度70
%の下で0.75以下でありかつフィルム表面粗度が平
均0.90μ/5mm以下であることを特徴とする二軸
配向の実質的にポリ−p−フェニレンスルフィドから成
るフィルム。
1. Coefficient of dynamic friction between films is 20℃, relative humidity is 70
A biaxially oriented film consisting essentially of poly-p-phenylene sulfide, characterized in that the film surface roughness is less than or equal to 0.75% and has an average film surface roughness of less than or equal to 0.90μ/5mm.
JP53108887A 1978-09-05 1978-09-05 Easy-slip film Expired JPS595101B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53108887A JPS595101B2 (en) 1978-09-05 1978-09-05 Easy-slip film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53108887A JPS595101B2 (en) 1978-09-05 1978-09-05 Easy-slip film

Publications (2)

Publication Number Publication Date
JPS5534968A JPS5534968A (en) 1980-03-11
JPS595101B2 true JPS595101B2 (en) 1984-02-02

Family

ID=14496106

Family Applications (1)

Application Number Title Priority Date Filing Date
JP53108887A Expired JPS595101B2 (en) 1978-09-05 1978-09-05 Easy-slip film

Country Status (1)

Country Link
JP (1) JPS595101B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59171601U (en) * 1983-05-02 1984-11-16 田浦 光正 Globe rotating hair iron

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57121052A (en) * 1981-01-22 1982-07-28 Toray Ind Inc Polyphenylene sulfide sheet -like material
JPS57205119A (en) * 1981-06-12 1982-12-16 Toray Ind Inc Biaxially stretched poly-p-phenylenesulfide film
JPS60231316A (en) * 1984-04-27 1985-11-16 松下電器産業株式会社 Capacitor
JPS60255978A (en) * 1984-06-01 1985-12-17 Toray Ind Inc Metallized film
US4777228A (en) * 1984-06-29 1988-10-11 Kureha Kagaku Kogyo Kabushiki Kaisha Biaxially oriented paraphenylene sulfide block copolymer film and process for producing the same
US4774298A (en) * 1984-06-29 1988-09-27 Kureha Kagaku Kogyo Kabushiki Kaisha Process for producing biaxially oriented paraphenylene sulfide block copolymer film
JPS6194314A (en) * 1984-10-15 1986-05-13 松下電器産業株式会社 Chip type metalized resin film capacitor
JPS61102020A (en) * 1984-10-25 1986-05-20 松下電器産業株式会社 Capacitor
JPS61102019A (en) * 1984-10-25 1986-05-20 松下電器産業株式会社 Capacitor
JPS61102022A (en) * 1984-10-25 1986-05-20 松下電器産業株式会社 Capacitor
JPS62242517A (en) * 1986-04-14 1987-10-23 Kureha Chem Ind Co Ltd Biaxially oriented poly-para-phenylene sulfide film
JPH0747295B2 (en) * 1986-11-20 1995-05-24 呉羽化学工業株式会社 Slippery polyary lentithioether film and process for producing the same
US5294660A (en) * 1988-03-07 1994-03-15 Toray Industries, Inc. Polyphenylene sulfide film and process of manufacturing the same
JPH01232608A (en) * 1988-03-11 1989-09-18 Diafoil Co Ltd Polyphenylene sulfide film for capacitor
EP0992531B1 (en) * 1997-06-20 2005-03-16 Nippon Zeon Co., Ltd. Polymer film and film capacitor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59171601U (en) * 1983-05-02 1984-11-16 田浦 光正 Globe rotating hair iron

Also Published As

Publication number Publication date
JPS5534968A (en) 1980-03-11

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