JPH05202274A - Thermoplastic polyester resin composition and film made therefrom - Google Patents

Thermoplastic polyester resin composition and film made therefrom

Info

Publication number
JPH05202274A
JPH05202274A JP1103292A JP1103292A JPH05202274A JP H05202274 A JPH05202274 A JP H05202274A JP 1103292 A JP1103292 A JP 1103292A JP 1103292 A JP1103292 A JP 1103292A JP H05202274 A JPH05202274 A JP H05202274A
Authority
JP
Japan
Prior art keywords
film
aluminum oxide
oxide particles
particles
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.)
Granted
Application number
JP1103292A
Other languages
Japanese (ja)
Other versions
JP2845249B2 (en
Inventor
Masatoshi Aoyama
雅俊 青山
Minoru Yoshida
実 吉田
Masaru Suzuki
勝 鈴木
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
Priority to JP1103292A priority Critical patent/JP2845249B2/en
Application filed by Toray Industries Inc filed Critical Toray Industries Inc
Priority to KR1019930702902A priority patent/KR100263613B1/en
Priority to EP19930902514 priority patent/EP0577846B1/en
Priority to DE1993624303 priority patent/DE69324303T2/en
Priority to PCT/JP1993/000073 priority patent/WO1993015145A1/en
Priority to DE1993633590 priority patent/DE69333590T2/en
Priority to EP19980114355 priority patent/EP0903375B1/en
Priority to CA002106755A priority patent/CA2106755A1/en
Priority to US08/119,075 priority patent/US6124031A/en
Publication of JPH05202274A publication Critical patent/JPH05202274A/en
Application granted granted Critical
Publication of JP2845249B2 publication Critical patent/JP2845249B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Magnetic Record Carriers (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

PURPOSE:To obtain the title compsn. useful for preparing an abrasion-resistant film for a magnetic recording medium, etc., by incorporating specific aluminum oxide particles into the compsn. CONSTITUTION:The title compsn. is prepd. by incorporating theta-aluminum oxide particles, pref. having a specific surface area, as a measure of the primary particle size, of 10m<2>/g or higher, still pref. 50m<2>/g or higher, and a secondary particle size of 0.01-2.0mum, still pref. 0.01-0.5mum, into the compsn.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は熱可塑性ポリエステル組
成物およびそれからなるフイルムに関する。さらに詳し
くは耐摩耗性に優れた磁気記録媒体用等のフイルムを得
るに適した熱可塑性ポリエステル組成物およびそれから
なるフイルムに関する。
FIELD OF THE INVENTION The present invention relates to a thermoplastic polyester composition and a film comprising the same. More specifically, it relates to a thermoplastic polyester composition suitable for obtaining a film having excellent abrasion resistance for magnetic recording media and the like, and a film comprising the same.

【0002】[0002]

【従来の技術】一般に熱可塑性ポリエステル、例えばポ
リエチレンテレフタレートは優れた力学的特性を有して
おり、フイルムなどの成形品として広く用いられてい
る。通常、該ポリエステルは、成形品に易滑性を付与す
る目的でポリエステル中に不活性粒子を含有せしめ、成
形品の表面に凹凸を付与する方法が行われている。この
ような不活性粒子としては種々あるが、一般に不活性粒
子は該ポリエステルとの親和性に欠け、耐摩耗性に劣る
といった問題があった。
2. Description of the Related Art Generally, thermoplastic polyesters such as polyethylene terephthalate have excellent mechanical properties and are widely used as molded articles such as films. Usually, for the purpose of imparting slipperiness to a molded product, the polyester is made to contain inert particles in the polyester, and a method of imparting unevenness to the surface of the molded product is performed. There are various kinds of such inert particles, but in general, there is a problem that the inert particles lack affinity with the polyester and have poor abrasion resistance.

【0003】従来からこの問題を解決すべく、不活性粒
子の表面処理の検討がなされており、例えば、特開昭6
3−221158号公報や特開昭63−280763号
公報(コロイダルシリカ粒子表面をグリコール基で改質
する)、特開昭63−312345号公報(コロイダル
シリカ粒子表面をカップリング剤で改質する)、特開昭
62−235353号公報(炭酸カルシウム粒子をリン
化合物で表面処理する)などが提案されている。
In order to solve this problem, the surface treatment of inert particles has been studied so far, for example, Japanese Patent Laid-Open Publication No. Sho-6.
3-221158, JP-A-63-280763 (the surface of colloidal silica particles is modified with a glycol group), and JP-A-63-313345 (the surface of colloidal silica particles is modified with a coupling agent). JP-A-62-235353 (wherein calcium carbonate particles are surface-treated with a phosphorus compound) has been proposed.

【0004】しかしながら、このような公知の方法をも
ってしても磁気テープのように繰り返し摩擦使用される
ような場合は、粒子の脱落を生じる。このため特殊な粒
子を使用することが最近提案されてきており、例えば、
特開昭62−172031号公報(シリコン粒子)、特
開平2−129230号公報(デルタ型酸化アルミニウ
ム粒子)などが提案されているが、いまだ不十分であ
る。
However, even if such a known method is used, when particles are repeatedly rubbed like a magnetic tape, particles fall off. Therefore, it has been recently proposed to use special particles, for example,
JP-A-62-172031 (silicon particles) and JP-A-2-129230 (delta-type aluminum oxide particles) have been proposed, but they are still insufficient.

【0005】[0005]

【発明が解決しようとする課題】本発明の目的は前記し
た従来技術の欠点を解消することにあり、特にシータ型
酸化アルミニウム粒子を熱可塑性ポリエステルに配合せ
しめて、フイルムを形成した場合、耐摩耗性に優れてい
るフイルムを得ることができる組成物およびそれからな
るフイルムを提供することにある。
An object of the present invention is to eliminate the above-mentioned drawbacks of the prior art, and particularly when theta type aluminum oxide particles are blended with a thermoplastic polyester to form a film, abrasion resistance is improved. It is an object of the present invention to provide a composition capable of obtaining a film having excellent properties and a film comprising the same.

【0006】[0006]

【課題を解決するための手段】前記した本発明の目的
は、シータ型酸化アルミニウム粒子を含有してなる熱可
塑性ポリエステル組成物およびそれからなるポリエステ
ルフイルムによって達成できる。
The above-mentioned object of the present invention can be achieved by a thermoplastic polyester composition containing theta type aluminum oxide particles and a polyester film comprising the same.

【0007】酸化アルミニウム粒子の結晶構造は、X線
回折法において、回折X線の現われる回折角2θ値から
同定できる。シータ型の結晶構造に対して、標準となる
2θ値の組は複数知られているが、主な2θ値は19.
4,31.3,32.7,36.7,39.2,44.
9,47.4,59.9,62.3,64.1,67.
2(度)などである。
The crystal structure of aluminum oxide particles can be identified by the diffraction angle 2θ value at which diffracted X-rays appear in the X-ray diffraction method. A plurality of sets of standard 2θ values are known for theta-type crystal structure, but the main 2θ values are 19.
4,31.3,32.7,36.7,39.2,44.
9, 47.4, 59.9, 62.3, 64.1, 67.
2 (degrees) or the like.

【0008】図1にシータ型の酸化アルミニウム粒子の
X線回折法の分析結果を示す。
FIG. 1 shows the analysis result of theta-type aluminum oxide particles by the X-ray diffraction method.

【0009】酸化アルミニウム粒子には、アルファ型、
ガンマ型、デルタ型、シータ型等、種々の結晶構造が知
られているが、それらは各粒子の合成法により決めるこ
とができる本発明のシータ型酸化アルミニウム粒子は例
えばみょうばんを炭酸塩中和後熱分解することにより生
成する。
Aluminum oxide particles include alpha type,
Various crystal structures such as gamma type, delta type and theta type are known, but they can be determined by the synthesis method of each particle. The theta type aluminum oxide particles of the present invention are, for example, after alum is neutralized with carbonate. It is generated by thermal decomposition.

【0010】酸化アルミニウム粒子の中で、特にシータ
型酸化アルミニウム粒子をポリエステルに配合すると、
フイルムにした際の耐摩耗性に非常に優れたものとな
る。この理由は不明であるが、本発明の結晶構造を有す
る酸化アルミニウム粒子がポリエステルとの親和性が高
いためではないかと考えられる。
Among the aluminum oxide particles, particularly when theta type aluminum oxide particles are blended with polyester,
It has excellent abrasion resistance when made into a film. The reason for this is unknown, but it is considered that the aluminum oxide particles having the crystal structure of the present invention have high affinity with polyester.

【0011】該粒子の一次粒子径は、極微細な粒子のた
めに測定がかなり困難であるが、比表面積では測定可能
である。本発明のシータ型酸化アルミニウムの比表面積
としては10m2 /g以上が好ましく、50m2 /g以
上がさらに好ましい。
The primary particle size of the particles is quite difficult to measure because of the extremely fine particles, but can be measured by the specific surface area. The specific surface area of the theta-type aluminum oxide of the present invention is preferably 10 m 2 / g or more, more preferably 50 m 2 / g or more.

【0012】このような粒子はポリエステル中では当然
のように凝集を引きおこしているが、二次粒子径は、熱
可塑性ポリエステル組成物から成型して得られるフイル
ムの目的に応じて任意に選ぶことができる。ただし、あ
まり大きすぎるとフイルム表面に粗大な突起が発生する
ため、好ましくは2.0μm以下、さらに好ましくは
0.5μm以下である。また、0.01μm以上である
ことが好ましい。
Naturally, such particles cause agglomeration in polyester, but the secondary particle diameter is arbitrarily selected according to the purpose of the film obtained by molding from the thermoplastic polyester composition. You can However, if it is too large, coarse protrusions are generated on the film surface, so that the thickness is preferably 2.0 μm or less, more preferably 0.5 μm or less. Further, it is preferably 0.01 μm or more.

【0013】なお、ここでいう二次粒子径とは、透過型
電子顕微鏡で粒子を1000個観察した際の円相当平均
径である。
The term "secondary particle diameter" as used herein means a circle-equivalent average diameter when 1,000 particles are observed with a transmission electron microscope.

【0014】シータ型酸化アルミニウム粒子の添加量と
しては、熱可塑性ポリエステル100重量部に対して
0.01〜10重量部が好ましく、さらには0.1〜5
重量部が好ましい。
The amount of theta-type aluminum oxide particles added is preferably 0.01 to 10 parts by weight, more preferably 0.1 to 5 parts by weight, based on 100 parts by weight of the thermoplastic polyester.
Parts by weight are preferred.

【0015】フイルムにした場合に耐摩耗性が良好であ
るためには、シータ型酸化アルミニウムの結晶構造の割
合が、50wt%以上が好ましく、70wt%以上が特
に好ましい。
In order to obtain good abrasion resistance when formed into a film, the proportion of the crystalline structure of theta-type aluminum oxide is preferably 50 wt% or more, particularly preferably 70 wt% or more.

【0016】本発明ににおける熱可塑性ポリエステルと
は、フイルムを成形し得るものならばどのようなもので
もよく、例えば、ポリエチレンテレフタレート、ポリテ
トラメチレンテレフタレート、ポリシクロヘキシレンジ
メチレンテレフタレート、ポリエチレン−2,6−ナフ
タレンジカルボキシレート、ポリエチレン−1,2−ビ
ス(2−クロルフェノキシ)エタン−4,4´−ジカル
ボキシレートあるいはポリエチレン−2,6−ナフタレ
ンジカルボキシレートが特に好ましい。
The thermoplastic polyester in the present invention may be any as long as it can form a film, for example, polyethylene terephthalate, polytetramethylene terephthalate, polycyclohexylene dimethylene terephthalate, polyethylene-2,6. -Naphthalenedicarboxylate, polyethylene-1,2-bis (2-chlorophenoxy) ethane-4,4'-dicarboxylate or polyethylene-2,6-naphthalenedicarboxylate are particularly preferred.

【0017】これらのポリエステルには、共重合成分と
して、アジピン酸、イソフタル酸、セバシン酸、フタル
酸、4,4´−ジフェニルジカルボン酸などのジカルボ
ン酸およびそのエステル形成性誘導体、ポリエチレング
リコール、ジエチレングリコール、ヘキサメチレングリ
コール、ネオペンチルグリコール、ポリプロピレングリ
コールなどのジオキシ化合物、p−(β−オキシエトキ
シ)安息香酸などのオキシカルボン酸およびそのエステ
ル形成性誘導体などを共重合してもかまわない。
These polyesters have, as copolymerization components, dicarboxylic acids such as adipic acid, isophthalic acid, sebacic acid, phthalic acid, 4,4'-diphenyldicarboxylic acid and ester-forming derivatives thereof, polyethylene glycol, diethylene glycol, Dioxy compounds such as hexamethylene glycol, neopentyl glycol and polypropylene glycol, oxycarboxylic acids such as p- (β-oxyethoxy) benzoic acid and ester-forming derivatives thereof may be copolymerized.

【0018】本発明の熱可塑性ポリエステル組成物は、
例えばシータ型酸化アルミニウム粒子をポリエステルの
出発原料であるグリコールを溶媒として混合攪拌して分
散スラリーとし、熱可塑性ポリエステルの反応系に添加
する製造方法などで得ることができる。なお、この際の
処理方法は攪拌によらずとも、例えば、超音波などによ
っても構わなく、また、サンドグラインダなどの媒体型
ミルを用いても構わない。
The thermoplastic polyester composition of the present invention comprises
For example, theta-type aluminum oxide particles can be obtained by a manufacturing method in which glycol, which is a starting material for polyester, is mixed and stirred to form a dispersion slurry, which is added to a reaction system of thermoplastic polyester. The treatment method at this time may be, for example, ultrasonic waves or the like instead of stirring, and a medium type mill such as a sand grinder may be used.

【0019】ポリエステルへの配合にあたっては、上記
した重合反応系に直接添加する方法以外にも、例えば、
シータ型酸化アルミニウム粒子を溶融状態のポリエステ
ルへ練り込む方法などでも可能である。前者の重合反応
系に添加する際の添加時期は任意であるが、エステル交
換反応前から重縮合反応の減圧開始前までの間が好まし
い。後者の練り込みの場合は、粒子を乾燥してポリエス
テルに練り込む方法でもスラリー状態で減圧しながら直
接練り込む方法でも構わない。
In addition to the above-mentioned method of directly adding to the polymerization reaction system, the polyester may be blended with
A method in which theta-type aluminum oxide particles are kneaded into molten polyester is also possible. The former may be added to the polymerization reaction system at any time, but is preferably from before the transesterification reaction to before the pressure reduction of the polycondensation reaction. In the case of the latter kneading, either a method of drying the particles and kneading into the polyester or a method of directly kneading in a slurry state under reduced pressure may be used.

【0020】本発明のポリエステルフイルムは次のよう
な方法によって製造することができる。
The polyester film of the present invention can be manufactured by the following method.

【0021】重合反応で得られたポリエステルのペレッ
トを十分乾燥した後ただちに押出機に供給する。このペ
レットを260〜350℃で溶融し、ダイよりシート状
に押出しキャスティングロール上で冷却、固化させて未
延伸フイルムを得る。次に、この未延伸フイルムを二軸
延伸するのが好ましい。延伸方法としては逐次二軸延伸
法、同時二軸延伸法、あるいはこのように二軸に延伸し
たフイルムを再度延伸する方法などを用いてもよい。ポ
リエステルの組成によるが、磁気記録媒体用フイルムと
して十分な弾性率を得るには最終的な延伸面積倍率(縦
倍率×横倍率)を6倍以上とすることが好ましい。
The polyester pellets obtained by the polymerization reaction are sufficiently dried and then immediately fed to the extruder. The pellets are melted at 260 to 350 ° C., extruded into a sheet form from a die, cooled on a casting roll and solidified to obtain an unstretched film. Next, it is preferable to biaxially stretch this unstretched film. As the stretching method, a sequential biaxial stretching method, a simultaneous biaxial stretching method, a method of stretching the biaxially stretched film again in this manner, or the like may be used. Although it depends on the composition of the polyester, it is preferable that the final stretched area ratio (longitudinal ratio × lateral ratio) be 6 times or more in order to obtain a sufficient elastic modulus as a film for a magnetic recording medium.

【0022】またフイルムの熱収縮率を小さく保つため
150〜260℃の温度範囲で0.1〜60秒程度の熱
処理を行なうことが好ましい。
Further, in order to keep the heat shrinkage rate of the film small, it is preferable to perform heat treatment in the temperature range of 150 to 260 ° C. for about 0.1 to 60 seconds.

【0023】本発明のフイルムは、単層フイルムとし
て、また積層フイルムとしてでも用いられる。積層フイ
ルムの場合、少なくとも一表面を構成するフイルムとし
て、本発明のフイルムを用いると、フイルム表面の耐摩
耗性、均一性、易滑性が良好となるので好ましい。フイ
ルムの積層方法としては溶融共押出しなど公知の方法を
用いることができる。
The film of the present invention can be used as either a single layer film or a laminated film. In the case of a laminated film, it is preferable to use the film of the present invention as the film constituting at least one surface, because the film surface will have good abrasion resistance, uniformity, and slipperiness. As a film laminating method, a known method such as melt coextrusion can be used.

【0024】積層フイルムにおける一表面を構成する本
発明のフイルム(以下、積層部ともいう)の厚さは、含
有する酸化アルミニウム粒子の二次粒子径に対して0.
1〜20倍にすることが、フイルム表面の均一性、易滑
性が特に良好となり好ましい。
The thickness of the film of the present invention (hereinafter, also referred to as a laminated portion) constituting one surface of the laminated film is 0. 0 with respect to the secondary particle diameter of the aluminum oxide particles contained therein.
It is preferable that the amount is from 1 to 20 times because the film surface uniformity and slipperiness are particularly good.

【0025】また、積層部のシータ型酸化アルミニウム
粒子の含有量は、0.05〜30重量部が好ましく、特
に0.1〜10重量部が好ましい。
The content of theta-type aluminum oxide particles in the laminated portion is preferably 0.05 to 30 parts by weight, particularly preferably 0.1 to 10 parts by weight.

【0026】[0026]

【実施例】次に、本発明を実施例および比較例により、
さらに詳細に説明する。
EXAMPLES Next, the present invention will be described with reference to Examples and Comparative Examples.
It will be described in more detail.

【0027】(1)酸化アルミニウム粒子の比表面積の
評価 B.E.T.法に従って測定した。
(1) Evaluation of Specific Surface Area of Aluminum Oxide Particles B. E. T. It measured according to the method.

【0028】(2)酸化アルミニウム粒子の二次粒子径
の評価 酸化アルミニウム粒子をポリエステルに配合せしめ、
0.2μm厚みの超薄切片にカッティング後、透過型電
子顕微鏡で観察し、凝集状態の二次粒子1000個の円
相当平均径(μm)で評価した。
(2) Evaluation of secondary particle size of aluminum oxide particles Aluminum oxide particles were blended with polyester,
After cutting into an ultrathin section having a thickness of 0.2 μm, the section was observed with a transmission electron microscope and evaluated by the circle-equivalent average diameter (μm) of 1000 secondary particles in an aggregated state.

【0029】(3)耐摩耗性の評価 得られたポリエステル組成物を実施例に示す方法で二軸
延伸フイルムとし、細幅にスリットしたテープ状ロール
をステンレス鋼SUS−304製カイドロールに一定張
力で高速、長時間こすりつけ、ガイドロール表面に発生
する白粉量によって次のようにランク付けし、1級を合
格とした。
(3) Evaluation of abrasion resistance The obtained polyester composition was made into a biaxially stretched film by the method shown in the examples, and a tape-shaped roll slit into a narrow width was applied to a stainless steel SUS-304 guide roll at a constant tension. It was rubbed at high speed for a long time and ranked as follows according to the amount of white powder generated on the surface of the guide roll, and the first grade was passed.

【0030】1級……白粉発生全くなし 2級……白粉発生少しあり 3級……白粉発生がかなり多い1st grade: No white powder generated 2nd grade: White powder slightly generated 3rd grade: White powder generated considerably

【0031】(4)表面凹凸の評価 得られたポリエステル組成物を通常の方法で二軸延伸フ
イルムとし、JISB0601に準じサーフコム表面粗
さ計を用い、針径2μm、荷重70mg、測定基準長0.
25mm、カットオフ0.08mmの条件下で中心線平均粗
さ(Ra)を測定した。
(4) Evaluation of surface irregularities The obtained polyester composition was made into a biaxially stretched film by a usual method, and a surfcom surface roughness meter according to JIS B0601 was used to measure a needle diameter of 2 μm, a load of 70 mg, and a measurement reference length of 0.
The center line average roughness (Ra) was measured under the conditions of 25 mm and a cutoff of 0.08 mm.

【0032】実施例1 B.E.T.表面積120m2 /gのシータ型酸化アル
ミニウム粒子を、10重量部、エチレングリコール90
重量部を混合して常温下1時間ディゾルバーで攪拌処理
し、シータ型酸化アルミニウム粒子/エチレングリコー
ルスラリー(A)を得た。
Example 1 B. E. T. 10 parts by weight of theta type aluminum oxide particles having a surface area of 120 m 2 / g, ethylene glycol 90
The weight parts were mixed and stirred at room temperature for 1 hour with a dissolver to obtain theta-type aluminum oxide particles / ethylene glycol slurry (A).

【0033】他方、ジメチルテレフタレート100重量
部、エチレングリコール64重量部に触媒として酢酸マ
グネシウム0.06重量部を加えてエステル交換反応を
行った後、反応生成物に先に調製したスラリー(A)4
重量部と、触媒の三酸化アンチモン0.03重量部およ
び耐熱安定剤としてトリメチルホスフェート0.03重
量部を加え、重縮合反応を行い、固有粘度0.615の
ポリエチレンテレフタレートを得た。透過型電子顕微鏡
による二次粒子径は0.15μmであった。
On the other hand, 0.06 parts by weight of magnesium acetate as a catalyst was added to 100 parts by weight of dimethyl terephthalate and 64 parts by weight of ethylene glycol to carry out an ester exchange reaction, and then the slurry (A) 4 prepared above was added to the reaction product.
By weight, 0.03 part by weight of antimony trioxide as a catalyst and 0.03 part by weight of trimethyl phosphate as a heat-resistant stabilizer were added to carry out a polycondensation reaction to obtain polyethylene terephthalate having an intrinsic viscosity of 0.615. The secondary particle diameter measured by a transmission electron microscope was 0.15 μm.

【0034】このポリエチレンテレフタレート組成物を
290℃で溶融、押し出しし、その後90℃で縦横それ
ぞれ3倍延伸し、さらにその後220℃で15秒間熱処
理し、厚さ15μmのポリエチレンテレフタレート二軸
延伸フイルムを得た。
This polyethylene terephthalate composition was melted at 290 ° C., extruded, and then stretched at 90 ° C. in the length and width three times each, and then heat treated at 220 ° C. for 15 seconds to obtain a biaxially stretched polyethylene terephthalate film having a thickness of 15 μm. It was

【0035】このフイルムを評価したところ、Ra=
0.011μm、耐摩耗性評価1級であり、耐摩耗性に
非常に優れたフイルムであった。
When this film was evaluated, Ra =
The film was 0.011 μm, the abrasion resistance was rated 1 grade, and the film was very excellent in abrasion resistance.

【0036】図1に、実施例1で使用したシータ型酸化
アルミニウム粒子のX線回折パターンを示した。
FIG. 1 shows the X-ray diffraction pattern of theta-type aluminum oxide particles used in Example 1.

【0037】実施例2〜4 ポリエチレンテレフタレート組成物中のシータ型酸化ア
ルミニウム粒子の比表面積、二次粒子径、添加量などを
変更し、実施例1と同様の方法で二軸延伸ポリエステル
フイルムを得た。これらのフイルムの評価結果を表1に
示した。これらのフイルムが良好な耐摩耗性を有してい
ることがわかる。
Examples 2 to 4 Biaxially stretched polyester films were obtained in the same manner as in Example 1 by changing the specific surface area, secondary particle size, addition amount and the like of theta type aluminum oxide particles in the polyethylene terephthalate composition. It was The evaluation results of these films are shown in Table 1. It can be seen that these films have good abrasion resistance.

【0038】実施例5 酸化アルミニウム粒子を添加しない以外は、全く実施例
1と同様にしてポリエチレンテレフタレート組成物
(X)を得た。
Example 5 A polyethylene terephthalate composition (X) was obtained in the same manner as in Example 1 except that aluminum oxide particles were not added.

【0039】実施例1のポリエチレンテレフタレート組
成物(Y)を(X)の上に溶融共押出して積層未延伸フ
イルムを得た。このときの押出し温度は290℃とし
た。その後90℃で縦横にそれぞれ3倍延伸し、さらに
その後220℃で20秒間熱処理し、積層二軸延伸フイ
ルムを得た。
The polyethylene terephthalate composition (Y) of Example 1 was melt-coextruded on (X) to obtain a laminated unstretched film. The extrusion temperature at this time was 290 ° C. After that, the film was stretched at 90 ° C. in the lengthwise and transverse directions three times, respectively, and further heat treated at 220 ° C. for 20 seconds to obtain a laminated biaxially stretched film.

【0040】(X),(Y)各層の厚みは、それぞれ8
μm,0.5μmであった。
The thickness of each of the layers (X) and (Y) is 8
μm and 0.5 μm.

【0041】このフイルムを評価したところ、表1に示
すようにRa=0.012μm、耐摩耗性評価1級であ
り、耐摩耗性に非常に優れたフイルムであった。
When this film was evaluated, as shown in Table 1, it was Ra = 0.012 μm, and the abrasion resistance was grade 1, and the film was very excellent in abrasion resistance.

【0042】[0042]

【表1】 比較例1〜5 粒子の種類および酸化アルミニウム粒子の結晶構造を変
更し、実施例1と同様の方法で二軸延伸ポリエステルフ
イルムを得た。これらのフイルムの評価結果を表2に示
した。これらのフイルムは、耐摩耗性が満足できるフイ
ルムではなかった。
[Table 1] Comparative Examples 1 to 5 Biaxially stretched polyester films were obtained in the same manner as in Example 1, except that the type of particles and the crystal structure of aluminum oxide particles were changed. The evaluation results of these films are shown in Table 2. These films were not satisfactory in abrasion resistance.

【0043】[0043]

【表2】 [Table 2]

【0044】[0044]

【発明の効果】本発明のポリエステル組成物は、特定の
結晶構造を有する酸化アルミニウム粒子を含有し、フイ
ルムとした場合、耐摩耗性に優れた効果を発揮する。
The polyester composition of the present invention contains aluminum oxide particles having a specific crystal structure, and when it is made into a film, it exhibits an excellent abrasion resistance.

【図面の簡単な説明】[Brief description of drawings]

【図1】図1は実施例1で使用したシータ型酸化アルミ
ニウム粒子のX線回折パターンを示す。
FIG. 1 shows an X-ray diffraction pattern of theta-type aluminum oxide particles used in Example 1.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】シータ型酸化アルミニウム粒子を含有して
なる熱可塑性ポリエステル組成物。
1. A thermoplastic polyester composition containing theta type aluminum oxide particles.
【請求項2】シータ型酸化アルミニウム粒子を含有して
なる熱可塑性ポリエステルフイルム。
2. A thermoplastic polyester film containing theta type aluminum oxide particles.
JP1103292A 1992-01-24 1992-01-24 Laminated polyester film Expired - Lifetime JP2845249B2 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
JP1103292A JP2845249B2 (en) 1992-01-24 1992-01-24 Laminated polyester film
EP19930902514 EP0577846B1 (en) 1992-01-24 1993-01-21 Thermoplastic polyester composition and film made therefrom
DE1993624303 DE69324303T2 (en) 1992-01-24 1993-01-21 THERMOPLASTIC POLYESTER COMPOSITION AND FILM MADE THEREOF
PCT/JP1993/000073 WO1993015145A1 (en) 1992-01-24 1993-01-21 Thermoplastic polyester composition and film made therefrom
KR1019930702902A KR100263613B1 (en) 1992-01-24 1993-01-21 Thermoplastic polyester composition and film made therefrom
DE1993633590 DE69333590T2 (en) 1992-01-24 1993-01-21 Thermoplastic polyester composition and film made therefrom
EP19980114355 EP0903375B1 (en) 1992-01-24 1993-01-21 Thermoplastic polyester composition and film made therefrom
CA002106755A CA2106755A1 (en) 1992-01-24 1993-01-21 Thermoplastic polyester composition and film made therefrom
US08/119,075 US6124031A (en) 1992-01-24 1993-01-27 Thermoplastic polyester composition and film made therefrom

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1103292A JP2845249B2 (en) 1992-01-24 1992-01-24 Laminated polyester film

Publications (2)

Publication Number Publication Date
JPH05202274A true JPH05202274A (en) 1993-08-10
JP2845249B2 JP2845249B2 (en) 1999-01-13

Family

ID=11766735

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1103292A Expired - Lifetime JP2845249B2 (en) 1992-01-24 1992-01-24 Laminated polyester film

Country Status (1)

Country Link
JP (1) JP2845249B2 (en)

Also Published As

Publication number Publication date
JP2845249B2 (en) 1999-01-13

Similar Documents

Publication Publication Date Title
JPH05301330A (en) Laminated film
EP0967068B1 (en) Biaxially oriented polyester film
JPS6369643A (en) Light-shielding laminated polyester film
JP2884990B2 (en) Polyester composition and film
JPH05202274A (en) Thermoplastic polyester resin composition and film made therefrom
JPH05302021A (en) Thermoplastic polyester composition film made therefrom
JPH05302020A (en) Thermoplastic polyester composition and film made therefrom
JPH101598A (en) Polyester composition and film
JP3271411B2 (en) Laminated polyester film
JPH05302019A (en) Thermoplastic polyester composition and film made therefrom
JP3239468B2 (en) Polyester composition and film comprising the same
JP3259444B2 (en) Polyester composition
JP3277587B2 (en) Thermoplastic polyester composition and film
JP3309497B2 (en) Polyester composition and film comprising the same
JPH03250043A (en) Production of polyester composition
JP3075932B2 (en) Polyester film
JPH10287800A (en) Polyester composition and film made therefrom
JP3254881B2 (en) Polyester composition
JP3521087B2 (en) Thermoplastic polyester film
JP3543972B2 (en) Polyester film
JP3239467B2 (en) Polyester composition and film comprising the same
JP3139128B2 (en) Thermoplastic polyester composition and polyester film comprising the same
JPH06287413A (en) Thermoplastic polyester composition and film made thereof
EP0674580A1 (en) Improved biaxially oriented copolyester film for magnetic recording media
JP3319058B2 (en) Method for producing polyester film

Legal Events

Date Code Title Description
FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20071030

Year of fee payment: 9

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081030

Year of fee payment: 10

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091030

Year of fee payment: 11

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091030

Year of fee payment: 11

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101030

Year of fee payment: 12

FPAY Renewal fee payment (prs date is renewal date of database)

Year of fee payment: 13

Free format text: PAYMENT UNTIL: 20111030

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121030

Year of fee payment: 14