JPS63168441A - Micro-cellular polyester film - Google Patents

Micro-cellular polyester film

Info

Publication number
JPS63168441A
JPS63168441A JP31389686A JP31389686A JPS63168441A JP S63168441 A JPS63168441 A JP S63168441A JP 31389686 A JP31389686 A JP 31389686A JP 31389686 A JP31389686 A JP 31389686A JP S63168441 A JPS63168441 A JP S63168441A
Authority
JP
Japan
Prior art keywords
film
polyester
polypropylene
stretching
present
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
JP31389686A
Other languages
Japanese (ja)
Inventor
Satoshi Otonari
音成 敏
Yoshiki Sato
嘉記 佐藤
Naruhiro Masuda
成裕 増田
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 JP31389686A priority Critical patent/JPS63168441A/en
Publication of JPS63168441A publication Critical patent/JPS63168441A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the title film which is inexpensive and light and is excellent in hiding property and whiteness, by mixing a crystalline polypropylene homopolymer having a melt flow index in a specified range with an aromatic polyester, extruding the mixture and stretching the extrudate. CONSTITUTION:3-20wt.% crystalline polypropylene homopolymer of a melt flow index of 0.2-120 is mixed with an aromatic polyester (e.g., polyethylene terephthalate or polybutylene terephthalate). This aromatic polyester is fed to an extruder, and melt-kneaded and extruded through a die to form a sheet. The obtained sheet is stretched at least uniaxially to form innumerable fine closed cells in the inside and surface of the film. In this way, the purpose micro- cellular polyester film can be obtained. This film can be suitably used for reverse-printed packaging materials, window decorating materials, etc.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、その表面及び内部に無数の微細気泡を含有せ
しめたポリエステルフィルムに関する。さらに詳しくは
、本発明は、微細な独立気泡を含有させることによυ単
位面積当りの重量が軽減されたフィルムであって、且つ
隠蔽性及び白色度に優れ次延伸ポリエステルフィルムに
関する。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a polyester film containing numerous microscopic bubbles on its surface and inside. More specifically, the present invention relates to a sub-stretched polyester film which has a reduced weight per υ unit area by containing fine closed cells, and which has excellent hiding properties and whiteness.

〈従来の技術と発明が解決しようとする問題点〉従来、
ポリエステルフィルムは、その優れた機械的特性、電気
的特性、耐薬品性、耐候性、耐熱性等を有することから
、各種産業において広く利用されているのは周知の通シ
である。とシわけ二軸配向ポリ(エチレンテレフタレー
ト)フィルムは、他のフィルムに較べ、特に寸法安定性
、平面化、弾性率等に優れ、又比較的安価で市場に提供
されることから、製版用あるいは情報産業基材用として
、今や欠くことのできない素材である。
<Problems to be solved by conventional technology and invention> Conventionally,
It is well known that polyester films are widely used in various industries because of their excellent mechanical properties, electrical properties, chemical resistance, weather resistance, heat resistance, etc. Biaxially oriented poly(ethylene terephthalate) film has excellent dimensional stability, flatness, elastic modulus, etc. compared to other films, and is available on the market at a relatively low price, so it is suitable for plate making or It is now an indispensable material for the information industry.

さて、近年の情報産業の進歩は著しく、各種各様の新商
品開発には目を見張るものがあり、例えば電子白板の登
場もその一つで、従来の黒板のイメージを一新したもの
といえる。即ち、白MKよる粉塵を追放しオフィス、会
議室のクリーン化に役立つと共に、複写機能を付与して
会議の効率化に寄与する画期的商品である。又、キャッ
シュレス時代の到来で、キャッシュカードやテレフォン
カード等の磁気カードの普及増大は著しい。
Now, the information industry has made remarkable progress in recent years, and the development of various new products is astounding.For example, the appearance of electronic whiteboards is one of them, and it can be said that the image of the conventional blackboard has been completely changed. . In other words, it is an epoch-making product that helps keep offices and conference rooms clean by eliminating dust caused by white MK, and also contributes to more efficient meetings by adding a copying function. Furthermore, with the advent of the cashless era, magnetic cards such as cash cards and telephone cards are becoming increasingly popular.

かかる商品の主要な一部材として、従来白色顔料例えば
酸化チタン微粒子を添加配合して白色且つ高隠蔽性を付
与し九二軸延伸ポリ(エチレンテレフタレート)フィル
ムが使用されていた。
Conventionally, as a major component of such products, a 92-axis stretched poly(ethylene terephthalate) film has been used, which has been blended with a white pigment such as fine particles of titanium oxide to impart white color and high hiding properties.

かかるフィルムは、その平面性や寸法安定性に優れるこ
とから電子白板においてはそのボード部に、又磁気カー
ドにおいてはその基材にと最終商品の最も重要な部分に
使われ、その優れた特性を遺憾無く発揮している。
Because of its excellent flatness and dimensional stability, such films are used in the most important parts of final products, such as the board part of electronic whiteboards and the base material of magnetic cards, and their excellent properties are used as the board part of electronic whiteboards and as the base material of magnetic cards. He is performing without regret.

しかしながら、その優れた特性をもつ、かかるフィルム
の場合でもその隠蔽力を上昇させるため白色顔料を多量
配合していることから、種種の弊害も生じている。すな
わちかかるフィルムの場合、比重の大きな無機粒子例え
ば微細な酸化チタン粒子を70重量%以上含有するため
、フィルムの見掛は比重はへ797−以上、ひいてはX
、Ot /−以上となり、単位体積当りの重量は2〜5
割も増大することから、所要面積のフィルム製品を取得
する場合スリット作業、搬送作業あるいは梱包作業とい
った製造作業における重労働を強いられていた。
However, even in the case of such a film having excellent properties, various disadvantages arise because a large amount of white pigment is blended in order to increase its hiding power. In other words, in the case of such a film, since it contains 70% by weight or more of inorganic particles having a large specific gravity, such as fine titanium oxide particles, the apparent specific gravity of the film is 797 or more, and thus X
, Ot /- or more, and the weight per unit volume is 2 to 5
Because of this, in order to obtain a film product with the required area, heavy labor during manufacturing operations such as slitting, transporting, or packaging was required.

又、単位体積当たシの重量の増大によシ、電子白板に使
用した場合、経時的にフィルムが弛んでくる、いわゆる
老化現象が起こシ、製品価値を著しく低下させる原因と
なる。
In addition, due to the increase in weight per unit volume, when used in electronic whiteboards, the film loosens over time, a so-called aging phenomenon, which significantly reduces product value.

一方、無機粒子が多量配合されることから、ポリエステ
ルフィルム自体の剛性が大きく々シ、フィルムのスリッ
ト加工や磁気カード等の製品にカッティング加工を施す
際フィルムのエツジ部で手を切るといった取扱い時の安
全性においても問題があった。そこで本発明者らは、か
かる諸問題を解決するにあたシ、まず見掛は比重をいか
Kして低減されるかが最大の改質ポイントとの着眼点に
立ち、素材自身を発泡体製造に関する研究に着手した。
On the other hand, since a large amount of inorganic particles are blended, the rigidity of the polyester film itself is greatly increased, and when handling the film, such as cutting one's hand on the edge of the film when slitting the film or cutting products such as magnetic cards, There were also safety issues. Therefore, in order to solve these problems, the present inventors first focused on the point that the most significant modification point was how to reduce the apparent specific gravity, and the material itself was made into a foam material. Started research on manufacturing.

すなわち、熱可塑性樹脂中にガス(気泡)を混入せしめ
、断熱材やクッション材に使用する発泡体製造処方等を
応用して発泡体構造にすれば、かなシの軽量化を図れる
はずである。
In other words, if gas (bubbles) is mixed into a thermoplastic resin and a foam structure is created by applying the foam manufacturing recipe used for insulation and cushioning materials, it should be possible to reduce the weight of the material.

従来ポリエステルに関する発泡体製造処方は数多く提案
されておシ、例えば特開昭5O−3♂765号公報、特
公昭j 7−4’ 44す6号公報、あるいは特開昭5
7−3弘り3/号公報等に記載されているようなガスあ
るいは気化可能な物質を添加して発泡体を製造する方法
や特開昭5コ−1AJr7/4j5公報あるいは特公昭
j?−!062!号公報等に記載されているような化学
的に分解してガスを発生する物質を添加し発泡化する方
法、更には特開昭J’/−!IIり53号公報あるいは
特公昭!コー276にを号公報に記載されているような
成型後液体を含浸又は溶剤に可溶な物質を抽出する方法
等が掲げられる。
Conventionally, many formulations for producing foams related to polyester have been proposed, such as JP-A-5O-3♂765, JP-A-Shoj 7-4'44-6, or JP-A-Sho.
A method of manufacturing a foam by adding a gas or a vaporizable substance as described in Publication No. 7-3 Hiro 3/3, etc., Japanese Patent Application Publication No. 1975-1AJr7/4j5 or Japanese Patent Application Publication No. 1972-1982. -! 062! A method of foaming by adding a substance that chemically decomposes to generate gas, as described in Japanese Patent Publication No. JP-A-Sho J'/-! IIri No. 53 Publication or Special Publication Show! Examples include a method of impregnating a molded material with a liquid or extracting a substance soluble in a solvent after molding, as described in Kou No. 276.

しかしながら、これらの発泡処方を、単純に二軸配向ポ
リエステルフィルムに適用するのは極めて難しい。なん
とならばかかる処方は成型体を製造するためのものであ
シ、いずれの処方を採用するにしても、フィルムの厚み
を考慮した場合数十ミクロン以下の気泡径で、しかも均
一な気泡に制御できる処方とは云い難たく、ましてや気
泡含有した押出シートを破断させることなく二軸延伸す
るには、あまりにもリスクが大きいと云わざるを得ない
。このことは、従来発泡ポリエステルニ軸延伸フィルム
に関する特許公報等で提案された例が殆んど見当らない
ことからも推察できよう。
However, it is extremely difficult to simply apply these foaming formulations to biaxially oriented polyester films. After all, such a formulation is for manufacturing a molded body, and no matter which formulation is adopted, the bubble diameter should be several tens of microns or less when the thickness of the film is taken into account, and the bubbles should be controlled to be uniform. It is difficult to say that this formulation is possible, and even more so, it is too risky to biaxially stretch an extruded sheet containing bubbles without breaking it. This can be inferred from the fact that there have been almost no examples proposed in patent publications regarding biaxially stretched foamed polyester films.

このように従来の発泡体製造処方を採用するのは至難で
あっても、二軸配向ポリエステルフィルム中に微細な気
泡を含有せしめることができれば見掛は比重の低減に有
効であることに違いはない。
Even though it is extremely difficult to adopt conventional foam manufacturing formulations, if it is possible to incorporate fine air bubbles into a biaxially oriented polyester film, it will be effective in reducing the apparent specific gravity. do not have.

しかも、数ミクロンから数十ミクロンの気泡径を無数に
含有せしめることができれば、気泡による透過光の散乱
が当然起こるはずであるから付随的に高隠蔽性フィルム
になることが予想され、白色顔料の配合量も当然少なく
できるであろうことから、見掛は比重の低減を助長する
と共に、剛性の抑制にもつながるであろう。従ってかか
るフィルムが得られれば、取扱作業時の重労働は軽減さ
れ、自重による弛み、いわゆる老化性に対しても、有効
なものとなる。しかも従来の発泡処方に捕われることな
く、簡便な方法で、かかるフィルムが得られるならば、
その1柴的価値は極めて大きい。
Moreover, if it is possible to contain an infinite number of bubbles with diameters ranging from several microns to several tens of microns, it is expected that the bubbles will naturally scatter the transmitted light, resulting in a film with high hiding properties. Naturally, the amount added can also be reduced, which will apparently help reduce specific gravity and also lead to suppression of rigidity. Therefore, if such a film is obtained, the heavy labor during handling will be reduced and it will be effective against loosening due to its own weight, so-called aging. Moreover, if such a film could be obtained by a simple method without being bound by conventional foaming formulations,
Its value is extremely great.

〈問題点を解決するための手段〉 本発明者らは、かかる実情に鑑み、微細気泡を無数に含
有するポリエステルフィルムを得んがため、鋭意研究を
重ねた結果、芳香族ポリエステルにポリオレフィン系ポ
リマーを配合するだけで、かかる目的に適うフィルムが
得られることを見い出し本発明に到達した。かかる本発
明は、特公昭5/−724432号公報にて、既に提案
された方法の範躊に含まれるものであるが、該公報は、
本来フィルム表面の筆記性及びマット調を付与せんがた
めに提案されたものであり、必ずしも本発明者らが意図
する微細気泡含有フィルムが得られるものではない。本
発明者らが得んとするフィルムを製造するためKは、特
定の極く限られたポリオレフィン系ポリマーでなければ
達成できないことを見い出し本発明に至った。
<Means for Solving the Problems> In view of the above circumstances, the present inventors have conducted extensive research in order to obtain a polyester film containing countless microbubbles, and as a result, the present inventors have found that aromatic polyester is combined with polyolefin polymer. The present inventors have discovered that a film suitable for such purposes can be obtained by simply blending the following, and have thus arrived at the present invention. This invention falls within the scope of the method already proposed in Japanese Patent Publication No. 5/724432;
This method was originally proposed to impart writability and a matte finish to the film surface, and it does not necessarily result in the microbubble-containing film intended by the present inventors. In order to produce the desired film, the present inventors discovered that K could only be achieved using a very specific specific polyolefin polymer, leading to the present invention.

すなわち、本発明の要旨は、メルトフローインデックス
(M、F、工)O0λ〜/−θの結晶性ポリグロピレン
ホモポリマーを3〜コθ重量%配合した芳香族ポリエス
テルをシート状に押出耳成形し、次いで該シートを少な
くとも一軸方向に延伸することによシ、該フィルムの表
面及び内部に微細な独立気泡を含有せしめたポリエステ
ルフィルムに存する。
That is, the gist of the present invention is to extrude an aromatic polyester containing 3 to 6% by weight of a crystalline polyglopylene homopolymer with a melt flow index (M, F, engineering) of 00λ to /-θ into a sheet shape. Then, by stretching the sheet in at least one axial direction, the polyester film contains fine closed cells on the surface and inside of the film.

かかる特定の結晶性ポリプロピレンホモポリマーを使用
することによシ1本発明者らが目的とする見掛は比重の
低減されたポリエステルフィルムを、工業的且つ安価に
製造できる。
By using such a specific crystalline polypropylene homopolymer, it is possible to industrially and inexpensively produce a polyester film with a reduced apparent specific gravity, which is the objective of the present inventors.

以下本発明の詳細な説明する。The present invention will be explained in detail below.

本発明でいう芳香族ポリエステルとは、テレフタル酸、
イソフタル酸、ナフタレンジカルボン酸のごとき芳香族
ジカルボン酸又はそのニステルト、エチレングリコール
、ジエチレングリコール、/、参−ブタンジオール、ネ
オペンチルグリコールのごときグリコールとを重縮合さ
せて製造されるポリエステルである。
The aromatic polyester referred to in the present invention refers to terephthalic acid,
It is a polyester produced by polycondensation of aromatic dicarboxylic acids such as isophthalic acid and naphthalene dicarboxylic acid, or their nisterates, and glycols such as ethylene glycol, diethylene glycol, dibutanediol, and neopentyl glycol.

これらのポリエステルは芳香族ジカルボン酸とグリコー
ルとを直接反応させて製造されるほか、芳香族ジカルボ
ン酸のアルキルエステルとグリコールとをエステル交換
反応させた後重縮合させるかあるいは芳香族ジカルボン
酸のジグリコールエステルを重縮合させる等の方法によ
っても製造できる。かかるポリエステルの代表例として
、ポリ(エチレンテレフタレート)やポリ(エチレン−
2,6−ナフタレート)あるいはポリ(ブチレンテレフ
タレート)等が挙げられる。
These polyesters are produced by directly reacting aromatic dicarboxylic acids and glycols, or by polycondensation after transesterification of alkyl esters of aromatic dicarboxylic acids and glycols, or by polycondensation of diglycols of aromatic dicarboxylic acids. It can also be produced by methods such as polycondensation of esters. Typical examples of such polyesters include poly(ethylene terephthalate) and poly(ethylene-terephthalate).
2,6-naphthalate) or poly(butylene terephthalate).

このポリエステルは、ホモポリマーであってもよく、ま
た第三成分を共重合したものでもよい。いずれにしても
本発明においてはエチレンテレフタレート単位及び/又
はエチレンーコ、6−す7タレ一ト単位及び/又はブチ
レンテレフタレート単位を70 m01%以上、好まし
くは/ Om01%以上、更に好ましくはりOmo1%
以上含有するポリエステルが好ましい。
This polyester may be a homopolymer or may be a copolymer of a third component. In any case, in the present invention, the content of ethylene terephthalate units and/or ethylene co, 6-7 thale units and/or butylene terephthalate units is 70 m01% or more, preferably /0m01% or more, and more preferably Omo1%.
Polyesters containing the above are preferred.

又、本発明においてはポリエステルの重合度が低すぎる
と、機械的強度が低下するので、その固有粘度は0.弘
以上、好ましくは0.j〜/、2、更に好ましくは0.
! j〜0.!!のものが好ましい。
Furthermore, in the present invention, if the degree of polymerization of the polyester is too low, the mechanical strength will decrease, so the intrinsic viscosity of the polyester will be 0. Hiroshi or higher, preferably 0. j~/, 2, more preferably 0.
! j~0. ! ! Preferably.

さて、通常ポリエステルをフィルム化する場合、フィル
ム間同志あるいはフィルムと金属ロール類間の滑り性す
なわち摩擦係数を低減して生産性や取扱い作業性を損な
わないようにするため、フィルム表面粗度付与剤、すな
わち微細な不活性粒子を適度に含有せしめたポリエステ
ルを用いるが、本発明に用いるポリエステルはかかる不
活性微粒子を含有しないものが好ましく使用される。な
ぜならば、該不活性微粒子によシ、得られたフィルムの
白色度や隠蔽性の制御に支障をきたす場合があるからで
ある。しかしながら、得んとするフィルムの要求特性に
支障がない限り、かかる不活性微粒子を含有したポリエ
ステルを使用しても何ら差しつかえはない。
Normally, when polyester is made into a film, a film surface roughening agent is used to reduce the slipperiness between the films or between the film and metal rolls, that is, the coefficient of friction, so as not to impair productivity and handling workability. That is, a polyester containing an appropriate amount of fine inert particles is used, but the polyester used in the present invention preferably does not contain such fine inert particles. This is because the inert fine particles may interfere with the control of the whiteness and hiding properties of the obtained film. However, there is no problem in using polyester containing such inert fine particles as long as it does not interfere with the required properties of the desired film.

本発明における必須構成成分としてのポリプロピレンは
、結晶性ポリプロピレンのホそポリマーであシ、シかも
特定のメルトフローインデックス(M、?、工、)を有
するものでなければならない。又かかるポリプロピレン
の配合量も特定の範囲が好ましい。なお、かかるポリプ
ロピレンのホモポリi−とは少なくとも? s mot
s以−ヒ、好ましくは9 ? mot%以上がプロピレ
ン単位を有するポリマーである。
Polypropylene, which is an essential component in the present invention, is a crystalline polypropylene polymer and must have a specific melt flow index (M, ?, M). It is also preferable that the amount of polypropylene blended is within a specific range. In addition, homopoly i- of such polypropylene is at least ? s mot
s - h, preferably 9? The polymer has mot% or more of propylene units.

すなわち、本発明で使用する、かかるポリプロピレンが
非晶性ポリプロピレンである場合、ポリエステル中に配
合して無定形7−ト状にすることはできるものの、得ら
れ九該シートの表面に該ポリプロピレンの一部がブリー
ドアウトしてキャスティングドラムや延伸ロール等の表
面に付着、汚染し、更にテンターでの横延伸時クリップ
外れ及び/又はクリップを汚染するため使用できない。
That is, when the polypropylene used in the present invention is amorphous polypropylene, although it can be blended into polyester to form an amorphous sheet, it is possible to It cannot be used because parts bleed out and adhere to and contaminate the surfaces of casting drums, stretching rolls, etc., and furthermore, the clips come off during transverse stretching in a tenter and/or the clips become contaminated.

又、かかるポリプロピレンが例えば/ moz%以上エ
チレンユニットをランダムあるいはブロック形態に共重
合されたポリマーである場合、本発明の目的である最終
的に得られる延伸フィルムの内部に微細気泡を無数に生
成含有せしめることができず、従って、該フィルムでは
、見掛は比重の低減は充分達成されない。ちなみに、ポ
リオレフィン系のフィルムや成型品を製造するのに使用
されるポリプロピレンは、衝撃強度やj1裂強度向上等
のために、通常共重合系ポリマーが今や主流となってい
るが、それら多種の銘柄のうち、本発明はホモポリマー
でなければ達成できない。
In addition, if such polypropylene is a polymer copolymerized with ethylene units in a random or block form, for example, at a moz% or more, it is possible to form and contain countless microbubbles inside the finally obtained stretched film, which is the object of the present invention. Therefore, the film does not seem to achieve a sufficient reduction in specific gravity. By the way, the polypropylene used to manufacture polyolefin films and molded products is now commonly copolymerized to improve impact strength and J1 crack strength, but there are many different brands of these. Of these, the present invention cannot be achieved without a homopolymer.

さて、本発明のかかるポリプロピレンのメルトフローイ
ンデックスは0.2〜/2θ、好ましくは0.5〜!’
0が好ましい。すなわち、メルトフローインデックスが
0.2未満だと生成する気泡が大き過ぎるためか、延伸
時破断が頻発し、最終的フィルムが得られないし、一方
かかるメルトフローインデックスが720を超えると、
テンターによる横延伸時クリップ外れが多発して生産性
に劣るため好ましくない。
Now, the melt flow index of the polypropylene of the present invention is 0.2~/2θ, preferably 0.5~! '
0 is preferred. That is, if the melt flow index is less than 0.2, the bubbles generated are too large, and breakage occurs frequently during stretching, making it impossible to obtain the final film.On the other hand, if the melt flow index exceeds 720,
This is not preferable because the clips frequently come off during lateral stretching using a tenter, resulting in poor productivity.

本発明のポリプロピレンの配合量は3〜,20重量%で
ある。すなわち、該配合量が3重量−未満だと、得られ
る最終的なフィルム中の微細気泡の生成、含有値が少な
く、見掛は比重の低減には、もはや有効ではなく、一方
コO重1にチを超えると、微細気泡の生成は増加するも
のの、生成気泡過多のためか、延伸時の破断が多くなり
好1しくない。
The amount of polypropylene used in the present invention is 3 to 20% by weight. That is, if the blending amount is less than 3% by weight, the final film obtained will have a small amount of microbubbles, and will no longer be effective in reducing the apparent specific gravity. If the stretching temperature exceeds 100, the generation of fine bubbles increases, but this is not preferable, as the number of breaks during stretching increases, probably due to the excessive number of bubbles generated.

本発明は、上述した芳香族ポリエステルと結晶性ポリプ
ロピレンホモポリマーを配合するが。
In the present invention, the above-mentioned aromatic polyester and crystalline polypropylene homopolymer are blended.

本発明の目的とする最終フィルムの表面及び内部に微細
な独立気泡を無数含有せしめるためには、更に、少なく
とも一軸方向に延伸することが必須である。
In order to contain numerous fine closed cells on the surface and inside of the final film, which is the object of the present invention, it is essential to further stretch the film in at least one direction.

すなわち、かかる配合物を単に押出成形して得たシート
の表面及び内部には、かかる微細な独立気泡は未だ生成
しておらず、その生成機構については必ずしも定かでは
ないが、延伸過程を経て初めて生成する。従って、従来
の発泡処方とは明らかに異なる処方と云える。かかる延
伸処方自体は特殊なものではなく、最終的には通常のポ
リエステルフィルムを製造する方法を、そのまま踏襲す
ればよい。
In other words, such fine closed cells have not yet been formed on the surface or inside of a sheet obtained by simply extrusion molding such a compound, and although the mechanism of their formation is not necessarily clear, it is only after the stretching process that such fine closed cells form. generate. Therefore, it can be said that the formulation is clearly different from conventional foaming formulations. The stretching recipe itself is not special, and the final method for producing a normal polyester film may be followed as it is.

すなわち、かかる配合物を原料として押出機にて250
〜300℃の温度で溶融混練し、ダイからシート状に押
出し、約70℃以下の温度に冷却して実質的に無定形の
シートとする。次いで該シート状物を、縦及び/又は横
方向に面積倍率で参倍以上、好ましくはり倍以上延伸し
更に/、2Q−120℃の温度で熱処理を行なうことに
より、製造できる。
That is, using such a blend as a raw material, an extruder produces 250
The mixture is melt-kneaded at a temperature of ~300°C, extruded through a die into a sheet, and cooled to a temperature of about 70°C or less to form a substantially amorphous sheet. The sheet-like material can then be stretched in the longitudinal and/or transverse directions by an area magnification of at least 3 times, preferably at least 1 times, and further heat-treated at a temperature of 2Q-120°C.

なお、かかる配合物原料の配合方法についても、%に限
定されるものではないが、予めポリエステルチップとポ
リプロピレンチップを混合ブレンドして押出機ホッパー
に投入してもよいが、押出機投入口にポリエステルチッ
プとポリプロピレンチップをそれぞれ定量的にフィード
する方法が最も簡便で配合比ムラも少ないことから好ま
しく採用される。
The blending method of such compound raw materials is not limited to %, but polyester chips and polypropylene chips may be mixed and blended in advance and charged into the extruder hopper. A method of quantitatively feeding chips and polypropylene chips is preferably adopted because it is the simplest method and there is less unevenness in the blending ratio.

さて、本発明は基本的にはポリエステルとポリプロピレ
ンとの配合によシ達成されるが、本発明の効果を損なわ
ない限り、その他の添加物等第三成分を配合しても何ら
差しつかえない。
Now, the present invention is basically achieved by blending polyester and polypropylene, but there is no problem in blending third components such as other additives as long as the effects of the present invention are not impaired.

かかる第三成分としては、例えば、抗酸化剤、帯電防止
剤、紫外線吸収剤、顔料、染料、滑剤、マット化剤、沁
光塘白剤等が挙げられ、必要に応じ適切女方法で必要量
添加すればよい。
Examples of such third components include antioxidants, antistatic agents, ultraviolet absorbers, pigments, dyes, lubricants, matting agents, and whitening agents. Just add it.

〈発明の効果〉 この様にして得られる本発明のポリエステルフィルムは
、該フィルムの表面及び内部に数ミクロン−数十ミクロ
ンという微細な独立気泡を無数含有するフィルムである
ことから、従来のポリエステルフィルムに比べひいては
約5割もの見掛は比重の低減を達成し、取扱い作業時の
重労働が野滅され、又含有2泡による緩衝効果のためか
フィルムエッチによる切傷事故も少なくなる。
<Effects of the Invention> The polyester film of the present invention obtained in this manner is a film containing numerous fine closed cells of several microns to several tens of microns on the surface and inside of the film, and therefore is superior to conventional polyester films. The apparent specific gravity has been reduced by about 50% compared to the original film, which eliminates heavy labor during handling, and also reduces accidents caused by film etching, probably due to the buffering effect of the two bubbles it contains.

又、本発明のポリエステルフィルムは、微細な気泡を無
数含有しているため、隠蔽性を付与するための酸化チタ
ン等の白色顔料を添加しないでも、後述する実施例から
明らかなようにかなりの隠蔽性及び白色度に優れるフィ
ルムとなり、顔料添加量をかなり低減できることは、見
掛は比重の低減に寄与するばかシではなく、生産性向上
の面からも大きなメリットとなる。すなわち、顔料を7
0重量%以上をも配合していた、従来の白色フィルムの
製造は通常のポリエステルフィルム製造に比べ、延伸倍
率の低下を余儀なくされておシ、又破断等によυ歩留シ
も低く、生産性に劣るものであったが、本発明を採用す
れば生産性は通常のフィルム並に向上する。
In addition, since the polyester film of the present invention contains numerous fine air bubbles, even without the addition of a white pigment such as titanium oxide to provide concealing properties, the polyester film of the present invention provides considerable concealment, as is clear from the examples described later. The fact that the film has excellent properties and whiteness, and the amount of pigment added can be considerably reduced does not appear to be a mere contribution to the reduction of specific gravity, but is also a great advantage in terms of improving productivity. That is, 7 pigments
Conventional production of white films, which contain more than 0% by weight, is forced to lower the draw ratio compared to normal polyester film production, and the yield rate is also low due to breakage, etc. However, if the present invention is adopted, the productivity will be improved to the same level as that of ordinary films.

更に、本発明のポリエステルフィルムは、その表面粗度
が大きく表面光沢の低い艶消しされたフィルムであり、
従来の白色フィルムでは得られなかった。独特の風合を
もつフィルムであること、一方通常のポリエステルフィ
ルムに比べ、熱収縮率は遜色なく、機械的強度は多少劣
るものの充分使用に耐えられるものである等の特性を有
し、従って今後各種の用途例えば裏刷り包装材や窓張シ
装飾材等の広範な分野で利用できる。又、本発明のポリ
エステルフィルムは気泡を包含したものであり、断熱材
としての分野での利用も期待できる。
Furthermore, the polyester film of the present invention is a matte film with high surface roughness and low surface gloss;
This was not possible with conventional white films. The film has a unique texture, has comparable heat shrinkage rate to regular polyester film, and although its mechanical strength is somewhat inferior, it is durable enough to withstand use in the future. It can be used in a wide range of fields such as back printing packaging materials and window decoration materials. Furthermore, since the polyester film of the present invention contains air bubbles, it can also be expected to be used in the field as a heat insulating material.

〈実施例〉 以下、本発明を実施例にて具体的に説明するが、本発明
は、その要旨を越えない限り、以下の実施例によって限
定されるものではない。なお、本発明における諸費性値
の測定方法及び製膜性評価方法は次に示す方法にて行な
った。
<Examples> Hereinafter, the present invention will be specifically explained using Examples, but the present invention is not limited by the following Examples unless the gist thereof is exceeded. Incidentally, the method for measuring the overhead value and the method for evaluating film formability in the present invention were carried out by the following methods.

(1)見掛は比重(f/ct/I);得られたフィルム
の任意の部分から20cm×20CInに切出し、マイ
クロメータで任意のり点の平均厚みを測定した後重量を
計って単位体積当りの重量を計算した。測定数はn=5
とし、その平均値を測定値とした。
(1) Appearance is specific gravity (f/ct/I); Cut out a 20 cm x 20 CIn piece from any part of the obtained film, measure the average thickness at any gluing point with a micrometer, then weigh it and calculate the per unit volume. The weight of was calculated. The number of measurements is n=5
The average value was taken as the measured value.

ク  ス (2)隠蔽度;マメペノ濃度計TD−タO弘型を使用し
、Gフィルタ下の透過光濃度を測定した。この値が大き
い程隠蔽力が高いことを示す。
(2) Hiding degree: The density of transmitted light under the G filter was measured using a Mamepeno densitometer TD-TAO Hiro model. The larger this value is, the higher the hiding power is.

(3)  白色度す値;日本軍色■社製色差計ND−K
 j型にて測定した。測定数11=Jとし、その平均値
を測定値とした。この値が(→側に大きいと黄味が強い
ことを示し、通常白色度を示す指標として用いられる値
である。。
(3) Whiteness value; Japanese military color ■ Color difference meter ND-K
Measured using J type. The number of measurements was 11=J, and the average value was taken as the measured value. If this value is large toward the → side, it indicates a strong yellowish tint, and is usually used as an index to indicate whiteness.

(4)光沢度(%) ;日本電色■社裂クロスメーター
VG−/θ7型を使用し、J工5Z−1’7弘の方法に
準じて測定した。黒色標準板を基準とし、入射角・反射
角60″における値を測定した。測定数はn=Jとし、
その平均値を測定値とした。
(4) Glossiness (%): Measured using a Nippon Denshoku ■Share crossmeter model VG-/θ7 according to the method of J. Ko. 5Z-1'7. Using a black standard plate as a reference, the values at an incident angle and a reflection angle of 60'' were measured.The number of measurements was n = J,
The average value was taken as the measured value.

(5)  表面粗度R5L (μm);■小板研究所製
表面粗さ測定器8に−JP型を使用し1,08B−〇6
θ/−/?74の方法に準じて測定した。詳細条件とし
て触針径2μm1触針圧30■、カットオフ値oJtm
s測定長Jjfiとし、測定数n=72行ない、最大最
小値を除いたn=/θの平均値を中心線平均粗さRa値
とした。
(5) Surface roughness R5L (μm); 1,08B-〇6 using a -JP type surface roughness measuring instrument 8 manufactured by Koita Institute.
θ/−/? It was measured according to the method of No. 74. Detailed conditions are stylus diameter 2μm, stylus pressure 30■, cutoff value oJtm
The measurement length was Jjfi, the number of measurements was n=72, and the average value of n=/θ excluding the maximum and minimum values was taken as the centerline average roughness Ra value.

(6)動摩擦係数μ(L ; A137M D−/7?
≠の方法に準じ平滑なガラス板上にフィルム同志を2枚
重ね、その上に荷重を載せ、2枚のフィルムの接圧を2
2/dとして、上側フィルムをII Orran /M
IXで走行させ、フィルム間の摩擦力を測定した。jW
R走行した点での摩擦係数を動摩擦係数μd値とした。
(6) Dynamic friction coefficient μ(L; A137M D-/7?
≠Place two films on top of each other on a smooth glass plate, place a load on top of it, and apply contact pressure between the two films to 2.
2/d, the upper film is II Orran /M
IX was run, and the frictional force between the films was measured. jW
The friction coefficient at the point where the vehicle ran in the R direction was defined as the dynamic friction coefficient μd value.

測定数はn=70とし、その平均値を測定値とした。The number of measurements was n=70, and the average value was taken as the measured value.

(7)引張破断強度(/y/md);インテスコ製引張
試験機を使用し、サンプル巾/!請にて、歪速度700
%/分で引張り、破断時の応力を測定した。測定数はn
 = sとし、その平均値から、単位断面積当りの強度
(kg/Ld )に換算して引張破断強度とした。
(7) Tensile strength at break (/y/md): Using an Intesco tensile tester, sample width/! At request, strain rate 700
%/min, and the stress at break was measured. The number of measurements is n
= s, and the average value was converted into the strength per unit cross-sectional area (kg/Ld) to obtain the tensile strength at break.

(8ン  熱収縮率(%);無張力状態で//θ℃雰囲
気中!分間熱処理し、その前後のサンプルの長さを測定
することにより次式にて計算した。
(Heat shrinkage rate (%): Calculated using the following formula by heat-treating for 1 minute in an atmosphere of 0.degree. C. under no tension and measuring the length of the sample before and after the treatment.

(9)  クリップ外れの評価;無定形シートを縦延伸
後、横延伸する際、横延伸機(テンター)の延伸点にお
いて、フィルム端部を固定するクリップから、縦延伸フ
ィルムが滑って外れる状況を次に示す3ランクにて判定
評価した。
(9) Evaluation of clip detachment: When an amorphous sheet is longitudinally stretched and then laterally stretched, the situation in which the longitudinally stretched film slips and comes off from the clips that fix the film ends at the stretching point of the horizontal stretching machine (tentter) is evaluated. Judgment and evaluation were performed according to the following three ranks.

この評価はつぎの(至)項と同様連続製膜性を示すもの
で、生産性の良否を判別する重要な項目である。
This evaluation, like the next (to) item, indicates continuous film forming performance, and is an important item for determining the quality of productivity.

ランク○:殆んどクリップ外れがなく生産性良好 27262時折りリップ外れが生じ、生産性に劣る ランク×:フイルムがズルズル清ってクリップ外れを起
こし、生産性が全 くない。
Rank ○: Good productivity with almost no clips coming off 27262 Occasional lip coming off, poor productivity Rank ×: The film slithers, causing clips coming off, and no productivity at all.

(4)破断性の評価;前(9)項と同様にテンターにお
いて、延伸時あるいは熱固定時にフィルムが破断する状
況を次に示す3ランクにて判定評価した。
(4) Evaluation of breakability: As in the previous item (9), the situation in which the film breaks during stretching or heat setting was evaluated using the following three ranks in a tenter.

ランク○:殆んどフィルム破断を起こさす生産性良好 ランクΔ:時折フィルム破断を生じ生産性に劣る ランクズ:常に破断を生じ生産性は全くない αυ メルト智フロー管インデックスM、?、工(y/
20rrtipr);  JIS  K−t7re−/
yr/ K単じて測定した。この値が高い程ポリマーの
溶融粘性が低いことを示す。
Rank ○: Good productivity, almost always causing film breakage Rank Δ: Occasional film breakage, poor productivity Rank: Always causing film breakage, no productivity αυ Melt wisdom flow tube index M, ? , engineering (y/
20rrtipr); JIS K-t7re-/
yr/K was measured alone. The higher this value is, the lower the melt viscosity of the polymer is.

実施例/ 極限粘度〔η) OJ、 62のポリ(エチレンテレフ
タレート)チップに対し、メルトフローインデックス(
M、F、工、)!の結晶性ポリプロピレンホモポリマー
チツブを70重量%配合し、均一にブレンドし九後、押
出機にて=り0℃で溶融し、lA0℃の冷却ドラム上で
冷却して650μm厚の見掛は比重7.27の無定形シ
ートを得た。
Example / Intrinsic viscosity [η) OJ, melt flow index (
M, F, Engineering,)! 70% by weight of crystalline polypropylene homopolymer chips were mixed, uniformly blended, melted in an extruder at 0°C, cooled on a cooling drum at 1A0°C, and had an apparent thickness of 650 μm. An amorphous sheet with a specific gravity of 7.27 was obtained.

次いで縦方向に2.り倍、横方向に3.2倍延伸した後
2≠j℃で6秒間熱処理し最終的にフィルム厚20θμ
mの二軸延伸フィルムを得た。
Then vertically 2. After stretching 3.2 times in the transverse direction, heat treatment was performed for 6 seconds at 2≠j℃, and the final film thickness was 20θμ.
A biaxially stretched film of m was obtained.

かかる延伸時の製膜性の評価結果及び最終的に得られた
フィルムの諸費性値を表7に示す。
Table 7 shows the evaluation results of film formability during stretching and the cost performance values of the finally obtained films.

表7に示すように、製膜時のクリップ外れ及び破断性は
いづれもランクOであり、生産性を損なうことはなかっ
た。一方、得られた該フィルムの見掛は比重は比較例/
に示す通常のポリエステルフィルム/、4A Oに対し
Ooり?であった。
As shown in Table 7, the clip removal and breakage properties during film formation were both ranked O, and productivity was not impaired. On the other hand, the apparent specific gravity of the obtained film was that of the comparative example/
Ordinary polyester film shown in /, 4A Oo? Met.

該フィルムの表面及び断面t−顕微鏡蜆察した結果、直
径/θ〜!θμ専の独立気泡が無数存在することをe′
誌した。なお、該フィルム化工程中サンプリングした無
定形シートでは独立気泡は認められなかった。
The surface and cross section of the film t - As a result of microscopic observation, the diameter / θ~! e' indicates that there are countless closed cells dedicated to θμ.
I published a magazine. Note that no closed cells were observed in the amorphous sheet sampled during the film forming process.

得られたフィルムの特性として、隠蔽度0JOsb値+
7./%光沢度37%であシ、比較例/の通常のポリエ
チレンテレフタレートフィルムに較べ、高隠蔽且つ白色
であり、 Raθ、34Lβ簿の表面凹凸を有する表面
光沢が抑えられたフィルムであった。フィルム表面の動
摩擦係数0.23の滑シのよいものであシ、又引張破断
強度72に9/−のしなやかな手触シを持つものであっ
た。熱収縮率は比較例/と殆んど変らず、寸法安定性に
も優れるフィルムであった。
The properties of the obtained film include a hiding degree of 0 JOsb value +
7. Compared to the normal polyethylene terephthalate film of Comparative Example, which had a gloss level of 37%, the film had high concealment and white color, and had surface irregularities of Raθ and 34Lβ, and had suppressed surface gloss. The film had a smooth surface with a coefficient of dynamic friction of 0.23, and had a tensile strength at break of 72 and a supple feel to the touch of 9/-. The heat shrinkage rate was almost the same as that of the comparative example, and the film had excellent dimensional stability.

実施例コ 実施例/中で使用したポリプロピレンの代シにM、F、
I、 27の結晶性ポリグロビレンホモボリマーを75
重量%及び螢光増白剤をθ、θ/重量%配合する以外は
、実施例/と同様にして、二軸延伸フィルムを得た。得
られた該フィルムの製膜性評価結果及びフィルム諸物性
値を表/に示す。フィルムの、1!!JIJ性は実施例
/と同様、クリップ外れ及び破断性共にう/り○であっ
た。
M, F, in place of the polypropylene used in Examples
I, 75 crystalline polyglobylene homopolymer of 27
A biaxially stretched film was obtained in the same manner as in Example except that θ and θ/weight % of the fluorescent brightener were blended. The film formability evaluation results and various physical property values of the obtained film are shown in Table 1. Film 1! ! The JIJ property was the same as in Example, and both clip removal and breakage properties were good/good.

得られたフィルムの見掛は比重はOJjであり、顕微@
i観察の結果実施例/と同様、直径70〜60μmの独
立気泡が無数−められた。該フィルムは実施例/とほぼ
同様の特性を有するものであった。更に詳しくは、実施
例/のb値+ /、/に較ベーコ、りと極めて白色度に
優れるものであり、又フィルム表面Ra O,6J’μ
m で光沢度25%と実施例/に較べ表面光沢が更に抑
えられたものでおった。
The apparent specific gravity of the obtained film was OJj, and it was observed under a microscope @
As a result of observation, numerous closed cells with a diameter of 70 to 60 μm were observed, as in Example. The film had almost the same characteristics as Example/. More specifically, the film has an extremely high whiteness compared to the b value + /, / of Example /, and the film surface Ra O, 6J'μ
m, the gloss level was 25%, and the surface gloss was further suppressed compared to Example.

実施例3 実施例/で使用したポリプロピレンの代F)KM、 ?
、工、八への結晶性ポリプロピレンホモポリマーを!重
fk%及び平均粒径0.3μmの酸化チタンをj重量%
配合する以外は、実施例/と同様にして二軸延伸フィル
ムを得た。得られた該フィルムの製膜性の評価結果及び
フィルム諸物性値を表/に示す。表/に示すように、フ
ィルムの製膜性は実施例/及びコと同様クリップ外れ及
び破断性共にランク○であった。又、得られた該フィル
ムの見掛は比重は/、コ0であシ、実施例/と同様、顕
微鏡観察の結果、直径20〜200μmの独立気泡が多
数認められた他に酸化チタン粒子による約l−=μmの
極微細な突起が同時に観察された。該フィルムは実施例
/とほぼ同様の特性を有するものであり、更に詳しくは
実施例/に較べ、隠蔽度が高く、表面光沢度の低いもの
であった。
Example 3 Substance of polypropylene used in Example/F) KM, ?
, Engineering, crystalline polypropylene homopolymer to eight! fk% by weight and j% by weight of titanium oxide with an average particle size of 0.3 μm.
A biaxially stretched film was obtained in the same manner as in Example except for blending. The evaluation results of the film formability of the obtained film and the values of various physical properties of the film are shown in Table 1. As shown in Table 1, the film formability of the film was ranked ○ in terms of clip release and breakage properties, as in Examples 1 and 2. In addition, the apparent specific gravity of the obtained film was 0, and as in Example 1, as a result of microscopic observation, a large number of closed cells with a diameter of 20 to 200 μm were observed, and in addition, a large number of closed cells with a diameter of 20 to 200 μm were observed. Ultrafine protrusions of approximately 1-=μm were observed at the same time. The film had almost the same characteristics as Example/, and more specifically, compared to Example/, it had a higher degree of hiding and a lower degree of surface gloss.

比較例/ 実施例/で使用したポリプロピレンを全く配合せ尤、極
限粘度〔η〕O9≦50の平均粒径0.7μmの炭酸カ
ルシウムQ、弘重量%含有するポリ(エチレンテレフタ
レート)チップを使用することを除いては、実施例/と
同様にして、二軸延伸フィルムを得た。得られたフィル
ムは、表/に示すように極〈一般的なポリエステルフィ
ルムであり、見掛は比重は1.参〇で、実施例/で述べ
たような独立気泡は認められなかった。
Comparative Example/A poly(ethylene terephthalate) chip containing the polypropylene used in Example/ without any of the polypropylene used, but containing Calcium Carbonate Q having an intrinsic viscosity [η]O9≦50 and an average particle size of 0.7 μm, and a % by weight, was used. A biaxially stretched film was obtained in the same manner as in Example except for this. The obtained film, as shown in Table 1, is a very common polyester film with an apparent specific gravity of 1. At No. 3, no closed cells as described in Example were observed.

フィルム外観は実施例/〜3の白色フィルムに対し、若
干濁った半透明のフィルムであった。
The appearance of the film was slightly cloudy and translucent, compared to the white film of Examples/-3.

比較例コ 実施例/で使用したホモポリプロピレンの代シにM、F
、■、22の? mo1%エチレンランダム共重合ポリ
プロピレンを70重量%配合する以外は実施例1と同様
にして二軸延伸フィルムを得た。得られた該フィルムは
表1に示すように、製膜性については実施例/〜3と同
様問題のないものであったが、見掛は比重は7.30で
あり、顕微鏡観察による独立気泡の生成はごくまばらに
点在するのみで、該ポリプロピレンが微分散しているだ
けのものであった。又該フィルムは実施例/〜3に較べ
白色度及び隠蔽力に極めて劣るものであった。
M and F were substituted for the homopolypropylene used in Comparative Example and Example.
, ■, 22? A biaxially stretched film was obtained in the same manner as in Example 1, except that 70% by weight of mo1% ethylene random copolymer polypropylene was blended. As shown in Table 1, the obtained film had no problems in film formability as in Examples/--3, but the apparent specific gravity was 7.30, and it was observed under a microscope that there were no closed cells. The formation of the polypropylene was only very sparsely scattered, and the polypropylene was only finely dispersed. Moreover, the film was extremely inferior in whiteness and hiding power compared to Examples/--3.

比較例J 実施例/で使用した結晶性ポリプロピレンの代シに非晶
性ポリグロビレンホモボリマーを5重量%配合する以外
は、実施例1と同様にして二軸延伸工程に供したところ
、テンターにおけるクリップ外れがランク×で、ズルズ
ル滑ってしまい、全くサンプルが得られなかった。
Comparative Example J A biaxial stretching process was performed in the same manner as in Example 1, except that 5% by weight of an amorphous polyglobylene homopolymer was added in place of the crystalline polypropylene used in Example. The clip came off in the tenter with a rank of ×, and it slipped, so no sample could be obtained.

比較例≠ 実施例1で使用したポリプロピレンの代シにM、F、1
./ j Oの結晶性ポリプロピレンホモポリマーを2
0重i%配合する以外は、実施例/と同様にして二軸延
伸工程に供した。該フィルム化工程での製膜性は、表1
に示すようにクリップ外れランクΔ及び破断性ランクΔ
であシ、生産性に劣るものであった。
Comparative example ≠ M, F, 1 in place of the polypropylene used in Example 1
.. / j O crystalline polypropylene homopolymer 2
A biaxial stretching process was performed in the same manner as in Example except that 0 weight i% was added. The film formability in the film forming process is shown in Table 1.
As shown in , the clip detachment rank Δ and breakability rank Δ
Unfortunately, productivity was poor.

比較例! 実施例/で使用したポリプロピレンの代シにM、F、工
、0.7の結晶性ポリプロピレンホモポリマーを5重t
%配合する以外は実施例/と同様にして二軸延伸工程に
供した。該フィルム化における製膜性はクリップ外れは
ランク○であるものの、テンター出口での破断性はラン
ク×であシ、度々フィルムの中央部及び端部の破断が発
生し、二軸延伸フィルムは得られなかった。
Comparative example! In place of the polypropylene used in Example, 5 layers of crystalline polypropylene homopolymer of M, F, engineering, 0.7 were added.
A biaxial stretching process was carried out in the same manner as in Example except that the composition was blended in %. The film formability in this film formation is ranked ○ in terms of clip detachment, but the breakability at the exit of the tenter is rank ×, and the film often breaks at the center and edges, and the biaxially stretched film is not good. I couldn't.

比較例6 実施例/で使用したポリプロピレンの代りにM、F、工
、/θの結晶性ポリグロビレンホモボリマーを/重量%
配合する以外は、実施例1と同様にして二軸延伸フィル
ムを得九。フィルム化工程中の製膜性は問題なかったが
、得られた該フィルムは、見掛は比重7.3♂で、顕微
ψ観察による独立気泡の生成は認められるものの散在す
る程度であり、フィルムの外観は半透明で、白色度に極
めて劣るものであった。
Comparative Example 6 Instead of the polypropylene used in Example /, M, F, engineering, /θ crystalline polyglobylene homopolymer was added /wt%
A biaxially stretched film was obtained in the same manner as in Example 1 except for blending. Although there were no problems with the film-forming properties during the film-forming process, the obtained film had an apparent specific gravity of 7.3♂, and although the formation of closed cells was observed by microscopic ψ observation, they were only scattered. The appearance was translucent and the whiteness was extremely poor.

比較例7 実施例/で使用したポリプロピレンの代シにM、F、工
、/!の結晶性ポリプロピレンホモポリマーを30重黄
チ配合する以外は実施例/と同様にして二軸延伸工程に
供したところ、製膜時のクリップ外れランクΔで時折り
リップ外れ現象を起こし、又クリップ外れを起こさない
時は破断が多発即ち破断性ランク×であり、最終的な二
軸延伸フィルムは得られなかった。
Comparative Example 7 In place of the polypropylene used in Example /, M, F, Engineering, /! When the biaxial stretching process was carried out in the same manner as in Example except that the crystalline polypropylene homopolymer was blended with 30 layers of yellow, the lip detachment phenomenon occasionally occurred at the clip detachment rank Δ during film formation, and the clip When no separation occurred, the film was broken frequently, that is, the breakability was ranked x, and the final biaxially stretched film could not be obtained.

比較例! 実施例1で使用したポリプロピレンの代りにM、F、■
、7.3の結晶性低密度ポリエチレンホモホリマーを/
Q重量%配合する以外は実施例/と同様にして二軸延伸
フィルムを得た。フィルム化工程中の製膜性はクリップ
外れランク△で生産性に劣るものであった。得られた該
フィルムの見掛は比重は7.23であり、顕微鏡観察に
よる独立気泡の生成は比較例コと同様極めてまばらに点
在するのみで、ポリエチレンが微分散されただけのもの
であった。従って、比較例コと同様半透明のフィルムで
あシ隠蔽力に劣るものであった。
Comparative example! M, F, ■ instead of polypropylene used in Example 1
, 7.3 crystalline low density polyethylene homopolymer /
A biaxially stretched film was obtained in the same manner as in Example except that Q% by weight was added. The film-forming property during the film-forming process was ranked △ due to clip detachment, and the productivity was poor. The apparent specific gravity of the obtained film was 7.23, and when observed under a microscope, closed cells were only scattered very sparsely, as in Comparative Example C, indicating that the polyethylene was only finely dispersed. Ta. Therefore, like Comparative Example 1, the film was semitransparent and had poor hiding power.

Claims (1)

【特許請求の範囲】[Claims] (1)メルトフローインデックス0.2〜120の結晶
性ポリプロピレンホモポリマーを3〜20重量%配合し
た芳香族ポリエステルを、シート状に押出成形し、次い
で該シートを少なくとも一軸方向に延伸することにより
、該フィルムの表面及び内部に微細な独立気泡を含有せ
しめたポリエステルフィルム。
(1) By extruding an aromatic polyester containing 3 to 20% by weight of a crystalline polypropylene homopolymer having a melt flow index of 0.2 to 120 into a sheet shape, and then stretching the sheet in at least one direction, A polyester film containing fine closed cells on the surface and inside the film.
JP31389686A 1986-12-27 1986-12-27 Micro-cellular polyester film Pending JPS63168441A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31389686A JPS63168441A (en) 1986-12-27 1986-12-27 Micro-cellular polyester film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31389686A JPS63168441A (en) 1986-12-27 1986-12-27 Micro-cellular polyester film

Publications (1)

Publication Number Publication Date
JPS63168441A true JPS63168441A (en) 1988-07-12

Family

ID=18046815

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31389686A Pending JPS63168441A (en) 1986-12-27 1986-12-27 Micro-cellular polyester film

Country Status (1)

Country Link
JP (1) JPS63168441A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0306960A2 (en) 1987-09-10 1989-03-15 Diafoil Hoechst Co., Ltd Magnetic card
JPH0229438A (en) * 1988-07-18 1990-01-31 Toray Ind Inc Polyester film and printing material for printer
EP0377513A2 (en) * 1989-01-06 1990-07-11 Illinois Tool Works Inc. Corrosion and split resistant plastic materials
JPH02258297A (en) * 1988-07-20 1990-10-19 Imperial Chem Ind Plc <Ici> Thermal transcription printing receiver sheet
JPH02284929A (en) * 1989-04-27 1990-11-22 Toray Ind Inc White polyester film
US5082900A (en) * 1989-03-29 1992-01-21 Chisso Corporation Opacified molded product
US5084519A (en) * 1990-02-20 1992-01-28 Chisso Corporation Stretched article having pearly gloss and process for preparing same
JPH04202540A (en) * 1990-11-30 1992-07-23 Toyobo Co Ltd Void-containing polyester film
US5660931A (en) * 1994-03-17 1997-08-26 Skc Limited Polymeric film with paper-like characteristics
EP0897947A3 (en) * 1997-08-12 1999-08-25 Mitsubishi Polyester Film Corporation Fine cell-containing polyester film
DE19540277B4 (en) * 1994-11-02 2007-04-19 Toyo Boseki K.K. Film with fine cavities and process for their preparation

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5118462A (en) * 1974-08-07 1976-02-14 Tokyo Shibaura Electric Co GEETOTAANOFUSAIRISUTANO KUDOSEIGYO SOCHI

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5118462A (en) * 1974-08-07 1976-02-14 Tokyo Shibaura Electric Co GEETOTAANOFUSAIRISUTANO KUDOSEIGYO SOCHI

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0306960A2 (en) 1987-09-10 1989-03-15 Diafoil Hoechst Co., Ltd Magnetic card
JPH0229438A (en) * 1988-07-18 1990-01-31 Toray Ind Inc Polyester film and printing material for printer
JPH02258297A (en) * 1988-07-20 1990-10-19 Imperial Chem Ind Plc <Ici> Thermal transcription printing receiver sheet
EP0377513A2 (en) * 1989-01-06 1990-07-11 Illinois Tool Works Inc. Corrosion and split resistant plastic materials
US5114638A (en) * 1989-03-29 1992-05-19 Chisso Corporation & Maruzen Petrochemical Co., Ltd. Process for producing an opacified molded product
US5082900A (en) * 1989-03-29 1992-01-21 Chisso Corporation Opacified molded product
JPH02284929A (en) * 1989-04-27 1990-11-22 Toray Ind Inc White polyester film
US5084519A (en) * 1990-02-20 1992-01-28 Chisso Corporation Stretched article having pearly gloss and process for preparing same
JPH04202540A (en) * 1990-11-30 1992-07-23 Toyobo Co Ltd Void-containing polyester film
JPH0625274B2 (en) * 1990-11-30 1994-04-06 東洋紡績株式会社 Cavity-containing polyester film
US5660931A (en) * 1994-03-17 1997-08-26 Skc Limited Polymeric film with paper-like characteristics
DE19540277B4 (en) * 1994-11-02 2007-04-19 Toyo Boseki K.K. Film with fine cavities and process for their preparation
EP0897947A3 (en) * 1997-08-12 1999-08-25 Mitsubishi Polyester Film Corporation Fine cell-containing polyester film

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