JPH07241906A - Biaxially oriented polyolefin film - Google Patents

Biaxially oriented polyolefin film

Info

Publication number
JPH07241906A
JPH07241906A JP3329194A JP3329194A JPH07241906A JP H07241906 A JPH07241906 A JP H07241906A JP 3329194 A JP3329194 A JP 3329194A JP 3329194 A JP3329194 A JP 3329194A JP H07241906 A JPH07241906 A JP H07241906A
Authority
JP
Japan
Prior art keywords
film
bag
ethylene
weight
butene
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
JP3329194A
Other languages
Japanese (ja)
Inventor
Koji Hirata
浩二 平田
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.)
Tokuyama Corp
Original Assignee
Tokuyama Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tokuyama Corp filed Critical Tokuyama Corp
Priority to JP3329194A priority Critical patent/JPH07241906A/en
Publication of JPH07241906A publication Critical patent/JPH07241906A/en
Pending legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

PURPOSE:To obtain a polyolefin film which is excellent in setability of bags in bag making operation, excellent in bag-breaking resistance of a sealed part by using in packing operation, and difficult to be broken as the bag even by vibration, impact, dropping, etc., when a package is transferred or handled. CONSTITUTION:A biaxially oriented polyolefin film is composed of ethylene- propylene copolymer of 1 to 4wt.% in ethylene content or ethylene-butene- propylene copolymer of 0.5 to 3.0wt.% in ethylene content and 4 to 15wt.% in butene-1 content. Its elongation percentage at 5kg/mm<2> tensile strength in MD direction is 30 to 150%, and preferablly 80 to 130%, and mts tensile modulus of elasticity in MD direction is 80 to 130kg/mm<2>, and preferablly 90 to 120kg/mm<2>.

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、溶断シール部の耐破袋
性に優れると共に製袋作業性および充填作業性に優れ、
しかも透明性と光沢に優れ、繊維製品や雑貨品、カタロ
グ・雑誌の封筒および重量のある青果物等の包装用途に
好適に使用できる二軸延伸ポリオレフィンフィルムに関
する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is excellent in bag-breaking resistance of a fusion-cut seal portion and in bag-making workability and filling workability.
Moreover, the present invention relates to a biaxially oriented polyolefin film which is excellent in transparency and gloss and can be suitably used for packaging textile products, general merchandise, envelopes of catalogs and magazines, and heavy fruits and vegetables.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】包装
用ポリオレフィンフィルムの代表として、二軸延伸ポリ
プロピレンフィルム(以下、OPPフィルムと記す)が
繊維製品や雑貨品等の包装に多量に使用されている。こ
れは、OPPフィルムが透明性と光沢に優れ、しかも機
械的強度が高いことから印刷性や製袋性および充填作業
性に優れるためである。しかし、OPPフィルムは、溶
断シール部において破断に至までの伸び率が10%以下
と非常に小さいことから、内容物の充填作業時に破袋し
やすいことや、包装物の移送や取扱いおよび落下時に振
動、衝撃等でも破袋しやすいことが欠点として挙げられ
ている。
2. Description of the Related Art Biaxially oriented polypropylene film (hereinafter referred to as OPP film) is widely used as a representative of polyolefin films for packaging in the packaging of textile products and miscellaneous goods. . This is because the OPP film is excellent in transparency and gloss, and has high mechanical strength, so that it is excellent in printability, bag-making property, and filling workability. However, since the OPP film has a very small elongation at break of 10% or less in the fusing and sealing part, it is easy to break the bag during the filling work of the contents, and when transferring, handling or dropping the package. It has been mentioned as a drawback that it is easy to break the bag even with vibration and shock.

【0003】OPPフィルムに伸び率を増加させる方法
として、延伸倍率を小さくする方法が考えられるが、通
常のOPPフィルム用の原料を用いて縦延伸倍率を40
0%以下とした場合は、延伸されたフィルム部分と未延
伸の部分が混在したまだら状態となり、均一な延伸を行
うことができない。よって、OPPフィルムにおいては
低倍率の二軸延伸フィルムを製作することは困難であ
る。
As a method of increasing the elongation of the OPP film, a method of reducing the stretching ratio can be considered. The longitudinal stretching ratio is 40 by using a normal raw material for the OPP film.
When the content is 0% or less, a stretched film portion and an unstretched portion are mixed to form a mottled state, and uniform stretching cannot be performed. Therefore, it is difficult to produce a low-magnification biaxially stretched film in the OPP film.

【0004】なお、耐破袋性に優れる包装用フィルムと
して、無延伸ポプロピレンフィルム(以下、CPPフィ
ルムと記す)がある。CPPフィルムは溶断シール部の
伸び率が非常に大きいことから破袋しにくい特徴を持っ
ているが、伸び率が大きい故に印刷性に難点がある。そ
の上、フィルムが大変柔らかいことから、製袋作業にお
いて袋の揃え性が劣る。同様に充填作業でもフィルムに
腰が不足していることから自動充填機に掛かりにくく自
動化しにくいという問題を抱えている。
An unstretched polypropylene film (hereinafter referred to as a CPP film) is a packaging film having excellent bag-breaking resistance. The CPP film has a feature that it is difficult to tear the bag because the stretch ratio of the fused cut portion is very large, but the CPP film has a problem in printability because the stretch ratio is large. In addition, since the film is very soft, bag alignment is poor in bag manufacturing work. Similarly, in filling work, there is a problem that it is difficult to automate the filling machine because of lack of rigidity in the film and it is difficult to automate.

【0005】従来の技術として、特公平5−81604
号公報および特公平5−82416号公報には、縦およ
び横方向の引張弾性率が15〜50kg/mm2のオレ
フィン系共重合体樹脂を使用したポリオレフィンフィル
ムが開示されている。このポリオレフィンフィルムは、
ビニロンフィルムに替わる柔軟性と透明性および機械的
強度に優れたフィルムとなっている。しかしながら、こ
のポリオレフィンフィルムは先に説明したCPPフィル
ムに近い引張弾性率を示しており、本発明者が目的とす
る溶断シール機による製袋作業性や充填作業性の点では
不十分である。
As a conventional technique, Japanese Patent Publication No. 5-81604
JP-B No. 5-82416 and JP-B No. 5-82416 disclose a polyolefin film using an olefin-based copolymer resin having a tensile elastic modulus in the longitudinal and transverse directions of 15 to 50 kg / mm 2 . This polyolefin film is
It is a film with excellent flexibility, transparency, and mechanical strength that can replace vinylon film. However, this polyolefin film exhibits a tensile elastic modulus close to that of the CPP film described above, and is insufficient in terms of bag-making workability and filling workability by the fusion cutting and sealing machine which the present inventor aims.

【0006】[0006]

【課題を解決するための手段】本発明者は、以上のよう
な状況に鑑み、溶断シール機における袋のシール部が少
なくとも1方向の耐破袋性に優れ、また、印刷性、製袋
作業性および充填作業性に優れ、しかも柔軟で、透明
性、光沢性に優れるポリオレフィンフィルムを得ること
を目的として研究を行ってきた。その結果、上記目的を
達成することに成功し本発明を完成させるに至った。
In view of the above circumstances, the present inventor has found that the sealing portion of the bag in the fusing and sealing machine is excellent in bag puncture resistance in at least one direction, and has good printability and bag making work. Has been researched for the purpose of obtaining a polyolefin film which is excellent in transparency and filling workability, is flexible, and is excellent in transparency and gloss. As a result, they succeeded in achieving the above object and completed the present invention.

【0007】即ち、本発明は、エチレン含有量が1〜4
重量%のエチレン−プロピレン共重合体、または、エチ
レン含有量0.5〜3.0重量%且つブテン−1含有量
4〜15重量%のエチレン−ブテン−プロピレン共重合
体からなり、MD方向の引張強度5kg/mm2におけ
る伸び率が30〜150%であり、MD方向の引張弾性
率が80〜130kg/mm2であることを特徴とする
二軸延伸ポリオレフィンフィルムである。
That is, the present invention has an ethylene content of 1 to 4
% Ethylene-propylene copolymer, or ethylene-butene-propylene copolymer having an ethylene content of 0.5 to 3.0% by weight and butene-1 content of 4 to 15% by weight. The biaxially stretched polyolefin film is characterized in that it has an elongation of 30 to 150% at a tensile strength of 5 kg / mm 2 and a tensile modulus of elasticity in the MD direction of 80 to 130 kg / mm 2 .

【0008】本発明の二軸延伸ポリオレフィンフィルム
は、エチレン含有量が1〜4重量%のエチレン−プロピ
レン共重合体、または、エチレン含有量0.5〜3.0
重量%且つブテン−1含有量4〜15重量%のエチレン
−ブテン−プロピレン共重合体(以下、これらを単にポ
リオレフィン系共重合体ともいう。)よりなる。本発明
で使用されるエチレン−プロピレン共重合体はエチレン
含有量が1〜4重量%、好ましくは1.5〜2.5重量
%のランダム共重合体であり、また、エチレン−ブテン
−プロピレン共重合体はエチレン含有量が0.5〜3.
0重量%且つブテン−1含有量が4〜15重量%、好ま
しくはエチレン含有量が1.0〜2.0重量%、ブテン
−1含有量が7〜10重量%のランダム共重合体であ
る。
The biaxially stretched polyolefin film of the present invention is an ethylene-propylene copolymer having an ethylene content of 1 to 4% by weight, or an ethylene content of 0.5 to 3.0.
It is composed of an ethylene-butene-propylene copolymer having a butene-1 content of 4 to 15% by weight (hereinafter, simply referred to as a polyolefin-based copolymer). The ethylene-propylene copolymer used in the present invention is a random copolymer having an ethylene content of 1 to 4% by weight, preferably 1.5 to 2.5% by weight, and an ethylene-butene-propylene copolymer. The polymer has an ethylene content of 0.5-3.
It is a random copolymer having 0% by weight and a butene-1 content of 4 to 15% by weight, preferably an ethylene content of 1.0 to 2.0% by weight and a butene-1 content of 7 to 10% by weight. .

【0009】上記したエチレン−プロピレン共重合体お
よびエチレン−ブテン−プロピレン共重合体において、
エチレン量もしくはブテン−1量が上記範囲よりも少な
い場合は、OPPフィルムと同様に均一な延伸フィルム
が得られないばかりか、溶断シール部の耐破袋性に劣る
ものとなるために好ましくない。また、エチレン量もし
くはブテン−1量が上記範囲よりも多い場合はフィルム
の機械的強度が不足すると共にCPPフィルムの場合と
同様に製袋作業性や充填作業性の点では不十分となるた
めに好ましくない。
In the above ethylene-propylene copolymer and ethylene-butene-propylene copolymer,
When the amount of ethylene or the amount of butene-1 is less than the above range, not only a uniform stretched film cannot be obtained as in the OPP film, but also the blow-cut resistance of the fusion-cut seal portion is deteriorated, which is not preferable. Further, when the ethylene amount or the butene-1 amount is larger than the above range, the mechanical strength of the film becomes insufficient and, in the same manner as in the case of the CPP film, bag forming workability and filling workability become insufficient. Not preferable.

【0010】本発明において使用されるポリオレフィン
系共重合体は、その物性を阻害しない範囲、例えば、5
モル%以内でエチレン、ブテン、プロピレン以外のα−
オレフィンを共重合成分として含んでいてもよい。ま
た、上記のポリオレフィン系共重合体の混合物、また
は、上記のポリオレフィン系共重合体と他のポリオレフ
ィンとの混合物も使用することができる。ポリオレフィ
ン系共重合体同士を混合するときは、その配合割合は任
意である。ポリオレフィン系共重合体と他のポリオレフ
ィンとを混合するときは、ポリオレフィン系共重合体を
70重量%以上、他のポリオレフィンを30重量%以下
とすることが本発明の効果を得るために好適である。他
のポリオレフィンとしてはポリエチレン、ポリプロピレ
ン、ポリブテン等を挙げることができる。
The polyolefin-based copolymer used in the present invention is in a range that does not impair its physical properties, for example, 5
Α-other than ethylene, butene and propylene within mol%
An olefin may be included as a copolymerization component. Also, a mixture of the above polyolefin copolymers or a mixture of the above polyolefin copolymers with other polyolefins can be used. When the polyolefin-based copolymers are mixed with each other, the mixing ratio is arbitrary. When the polyolefin-based copolymer and the other polyolefin are mixed, it is preferable that the content of the polyolefin-based copolymer is 70% by weight or more and the content of the other polyolefin is 30% by weight or less in order to obtain the effects of the present invention. . Examples of other polyolefins include polyethylene, polypropylene and polybutene.

【0011】本発明で使用されるポリオレフィン系共重
合体、その混合物のメルトインデックスは、特に制限さ
れないが、良好なフィルム成形性を付与するためには
0.5〜10g/10分、さらに1〜5g/10分の範
囲とすることが好ましい。
The melt index of the polyolefin copolymer and the mixture thereof used in the present invention is not particularly limited, but in order to impart good film moldability, it is 0.5 to 10 g / 10 minutes, and further 1 to The range is preferably 5 g / 10 minutes.

【0012】本発明の二軸延伸ポリオレフィンフィルム
は、MD方向の引張強度5kg/mm2における伸び率
が30〜150%、好ましくは80〜130%であり、
MD方向の引張弾性率が80〜130kg/mm2、好
ましくは90〜120kg/mm2である。なお、MD
方向とは、二軸延伸ポリオレフィンフィルムの巻取方向
である。MD方向の引張強度5kg/mm2における伸
び率が30%よりも小さいか、または、MD方向の引張
弾性率が130kg/mm2よりも大きい場合は、溶断
シール部の耐破袋性に劣るものとなるために好ましくな
い。一方、MD方向の引張強度5kg/mm2における
伸び率が150%よりも大きいか、または、MD方向の
引張弾性率が80kg/mm2よりも小さい場合は、フ
ィルムの機械的強度が不足すると共にCPPフィルムの
場合と同様に製袋作業性や充填作業性の点で不十分とな
るために好ましくない。
The biaxially stretched polyolefin film of the present invention has an elongation at MD tensile strength of 5 kg / mm 2 of 30 to 150%, preferably 80 to 130%.
The tensile elastic modulus in the MD direction is 80 to 130 kg / mm 2 , preferably 90 to 120 kg / mm 2 . In addition, MD
The direction is the winding direction of the biaxially stretched polyolefin film. If the elongation at MD tensile strength of 5 kg / mm 2 is less than 30%, or the tensile elastic modulus in MD is greater than 130 kg / mm 2 , the fracturing resistance of the fusing seal is inferior. Is not preferable. On the other hand, if the elongation at MD tensile strength of 5 kg / mm 2 is greater than 150% or the tensile elastic modulus in MD is less than 80 kg / mm 2 , the mechanical strength of the film becomes insufficient and Similar to the case of the CPP film, it is not preferable in terms of bag making workability and filling workability, which is not preferable.

【0013】本発明の二軸延ポリオレフィンフィルムは
二軸延伸されている。延伸倍率は特に制限されるもので
はないが、MD方向で2〜4倍であることが好ましく、
3.5〜3.8倍であることがさらに好ましい。また、
TD方向では8〜12倍の範囲であることが好ましく、
9.0〜10.5の範囲であることがさらに好ましい。
The biaxially stretched polyolefin film of the present invention is biaxially stretched. The stretching ratio is not particularly limited, but is preferably 2 to 4 times in the MD direction,
More preferably, it is 3.5 to 3.8 times. Also,
It is preferably 8 to 12 times in the TD direction,
More preferably, it is in the range of 9.0 to 10.5.

【0014】本発明の二軸延伸ポリオレフィンフィルム
の厚みは特に限定されるものではないが、溶断シール部
の耐破袋性、製袋作業性、充填作業性を勘案すると、1
5〜120μmが好ましく、25〜60μmの範囲であ
ることがより好ましい。
The thickness of the biaxially stretched polyolefin film of the present invention is not particularly limited, but in consideration of the bag breakage resistance, bag making workability and filling workability of the fusion-cut seal portion, it is 1
It is preferably 5 to 120 μm, and more preferably 25 to 60 μm.

【0015】本発明の二軸延伸ポリオレフィンフィルム
は単層フィルムであってもよく、また、2層以上の積層
フィルムであってもよい。積層フィルムとすることで、
ヒートシール性、異スリップ性、ガスバリヤー性等の物
性を付与することができる。積層フィルムにする場合
は、本発明の二軸延伸ポリオレフィンフィルムに積層す
るフィルムの厚みは積層フィルムの20%以下にするこ
とが、その性能を損なわないので好ましい。
The biaxially stretched polyolefin film of the present invention may be a monolayer film or a laminated film having two or more layers. By using a laminated film,
Physical properties such as heat-sealing property, different slip property, and gas barrier property can be imparted. In the case of a laminated film, it is preferable that the thickness of the film laminated on the biaxially oriented polyolefin film of the present invention is 20% or less of the laminated film because the performance is not impaired.

【0016】この際、積層する樹脂はポリオレフィンに
限定されず、積層フィルムに付与する物性に応じて公知
の樹脂を採用することができる。例えば、ヒートシール
性を付与する場合には、本発明に用いるポリオレフィン
系共重合体よりも低温で溶融する樹脂、例えば、エチレ
ン含有量4〜8重量%、メルトインデックスが4〜12
g/10分のエチレン−プロピレンランダム共重合体を
積層すればよい。
At this time, the resin to be laminated is not limited to polyolefin, and a known resin can be adopted depending on the physical properties imparted to the laminated film. For example, in the case of imparting heat sealability, a resin that melts at a temperature lower than that of the polyolefin-based copolymer used in the present invention, for example, an ethylene content of 4 to 8 wt% and a melt index of 4 to 12 is used.
A g / 10 min ethylene-propylene random copolymer may be laminated.

【0017】また、2〜3層の積層フィルムにおいて、
外層より内層に滑剤を多く添加することでフィルムの内
面の滑性を小さくし、外面の滑性を大きくすることが可
能となり、内容物を容易に充填することができるように
なると共に内容物の有無に拘らず袋を重ねて積み上げた
ときに袋の棚崩れを防止できる。
Further, in a laminated film of 2 to 3 layers,
By adding more lubricant to the inner layer than to the outer layer, it is possible to reduce the lubricity of the inner surface of the film and increase the lubricity of the outer surface, and it becomes possible to easily fill the contents and Regardless of the presence or absence, it is possible to prevent the bags from collapsing when stacked.

【0018】さらに、ガスバリヤー性能を付与するため
に、共押出法等によりフィルムの片面にエチレン−ビニ
ルアルコール共重合体、例えば、株式会社クラレ製の商
品名「エバール」を接着樹脂を介在させて積層すること
もできる。この場合、エチレン−ビニルアルコール共重
合体を積層する面は外面であることが本発明の効果を妨
げないために好ましい。
Further, in order to impart a gas barrier property, an ethylene-vinyl alcohol copolymer, for example, "EVAL" manufactured by Kuraray Co., Ltd., is used on one side of the film by an adhesive resin by a coextrusion method or the like. It can also be laminated. In this case, it is preferable that the surface on which the ethylene-vinyl alcohol copolymer is laminated is the outer surface in order not to impair the effects of the present invention.

【0019】本発明に使用する各種の樹脂には公知の添
加剤、例えば、酸化防止剤、結晶核剤、熱安定剤、離型
剤、スリップ剤、ブロッキング防止剤や帯電防止剤を使
用することができる。ブロッキング防止剤としては、シ
リカ、天然ゼオライト、合成ゼオライト、カオリン、タ
ルク、シリコーン樹脂、シリコーンゴム、溶融シリカ、
メラミン樹脂、アクリル樹脂等の微粒子を使用するとよ
い。これらの微粒子は球形のものが好ましく、さらに
は、ポリオレフィン系共重合体より柔らかいゴム系のも
のがより好ましい。スリップ剤は、高級脂肪酸アミド系
を使用することができるが、多量に添加するとフィルム
が白化し、透明性と光沢を失う危険性があるので注意を
要する。帯電防止剤を適量添加すると静電気の発生を抑
えることができる。コロナ処理を行うとより効果が向上
するとともに印刷性やラミネート加工性も付与できる。
防曇剤を適量添加すると、本発明に使用するポリオレフ
ィン系共重合体は防曇効果が発現しやすく、袋の内面が
コロナ未処理でも防曇効果に優れ、青果物の包装用途に
十分使用可能となる。
Known additives such as antioxidants, crystal nucleating agents, heat stabilizers, release agents, slip agents, antiblocking agents and antistatic agents should be used for various resins used in the present invention. You can As the antiblocking agent, silica, natural zeolite, synthetic zeolite, kaolin, talc, silicone resin, silicone rubber, fused silica,
Fine particles such as melamine resin and acrylic resin may be used. These fine particles are preferably spherical, and more preferably rubber-based, which is softer than the polyolefin-based copolymer. As the slip agent, higher fatty acid amide type can be used, but it should be noted that if added in a large amount, there is a risk of whitening of the film and loss of transparency and gloss. Generation of static electricity can be suppressed by adding an appropriate amount of antistatic agent. When the corona treatment is performed, the effect is further improved and printability and laminating processability can be imparted.
When an appropriate amount of anti-fog agent is added, the polyolefin-based copolymer used in the present invention easily exhibits an anti-fog effect, and the inner surface of the bag has excellent anti-fog effect even without corona treatment, and can be sufficiently used for packaging of fruits and vegetables. Become.

【0020】本発明の二軸延伸ポリオレフィンフィルム
は、次の方法で製造することができる。まず、ポリオレ
フィン系共重合体を押出機にて溶融、混練し、溶融した
樹脂をT型ダイスにて冷却ロール上でシート状に冷却固
化する。得られたシートを縦延伸機にて加熱後2〜4倍
に延伸し、引き続き横延伸機にて加熱後、幅方向に8〜
12倍延伸する。横延伸後に延伸温度より幾分高めの温
度で5〜15%リラックスさせると溶断シール部の縮み
を改善することができ好ましい。
The biaxially stretched polyolefin film of the present invention can be manufactured by the following method. First, a polyolefin-based copolymer is melted and kneaded with an extruder, and the melted resin is cooled and solidified into a sheet on a cooling roll with a T-type die. The obtained sheet is heated by a longitudinal stretching machine and stretched 2 to 4 times, and subsequently heated by a transverse stretching machine and then 8 to 8 in the width direction.
Stretch 12 times. It is preferable to relax 5 to 15% at a temperature slightly higher than the stretching temperature after the transverse stretching because the shrinkage of the fusion-cut seal portion can be improved.

【0021】[0021]

【発明の効果】本発明の二軸延伸ポリオレフィンフィル
ムは、製袋作業において袋の揃え性に優れると共に充填
作業時において溶断シール部の耐破袋性に優れ、かつ、
包装物の移送時や取扱い時に振動、衝撃および落下等に
おいても破袋しにくい。また、透明性、光沢についても
従来のフィルムに劣らない優れた性能を保持している。
したがって、本発明の二軸延伸ポリオレフィンフィルム
は、一般の包装用フィルムとして好適に使用できる他、
繊維製品や雑貨品、カタログ・雑誌の封筒および重量の
ある青果物の包装袋として好適に使用することができ
る。
The biaxially stretched polyolefin film of the present invention is excellent in bag alignment during bag-making work, and also has excellent bag breakage resistance of the fusing seal portion during filling work, and
Difficult to tear the bag against vibration, shock and drop when transferring or handling the package. In addition, it has excellent performance in terms of transparency and gloss, which is not inferior to conventional films.
Therefore, the biaxially oriented polyolefin film of the present invention can be suitably used as a general packaging film,
It can be suitably used as textiles and miscellaneous goods, envelopes for catalogs and magazines, and packaging bags for heavy fruits and vegetables.

【0022】[0022]

【実施例】以下に、本発明を具体的に説明するために実
施例および比較例を掲げるが、本発明はこれら実施例に
限定されるものではない。なお、以下の実施例および比
較例におけるフィルムの物性は下記の方法により行っ
た。
EXAMPLES Examples and comparative examples are given below to specifically describe the present invention, but the present invention is not limited to these examples. The physical properties of the films in the following examples and comparative examples were measured by the following methods.

【0023】(1)引張り強度および伸び率 試料を10mm幅の短冊状に切断し、測定長を40mm
として引張試験機によって引張速度300mm/分、チ
ャート速度300mm/分でチャート紙に記録した。基
点より5kg/mm2の伸び率を読み取った。
(1) Tensile strength and elongation The sample was cut into a strip with a width of 10 mm, and the measurement length was 40 mm.
Was recorded on a chart paper at a tensile speed of 300 mm / min and a chart speed of 300 mm / min. The elongation of 5 kg / mm 2 was read from the base point.

【0024】(2)引張弾性率 試料を10mm幅の短冊状に切断し、測定長を20mm
として引張試験機によって引張速度20mm/分、チャ
ート速度2000mm/分で立上がり角度をチャート紙
に記録した。基点より20mmの点で垂線を引き、接線
との交点の強度を読み取り、下式により引張弾性率を算
出した。
(2) Tensile modulus The sample was cut into strips with a width of 10 mm, and the measurement length was 20 mm.
The rising angle was recorded on the chart paper by a tensile tester at a tensile speed of 20 mm / min and a chart speed of 2000 mm / min. A perpendicular line was drawn at a point 20 mm from the base point, the strength at the intersection with the tangent line was read, and the tensile elastic modulus was calculated by the following formula.

【0025】引張弾性率(kg/mm2)=〔強度(k
g)×試料長(mm)×チャート速度(mm/分)〕÷
〔引張り速度(mm/分)×20mm×フィルム厚み
(mm)×フィルム幅(mm)〕 (3)落下破袋率 共栄株式会社製PP−500型 OPPフィルム用溶断
刃を取り付けた溶断シール機にて、溶断シール温度38
0℃、製袋速度80枚/分の条件で袋寸法250×30
0mmの袋を製造した。この袋にジャガイモ1kgを入
れ、高さ0.75mより床面に自然落下させた。床面は
東洋リノリュウム社製の塩ビタイルを用いた。評価方法
は同一袋で15回まで落下させ、破袋までの落下回数を
計測した。試験回数を10回とし、下記式により破袋率
を算出した。
Tensile modulus (kg / mm 2 ) = [strength (k
g) x sample length (mm) x chart speed (mm / min)] ÷
[Pulling speed (mm / min) × 20 mm × Film thickness (mm) × Film width (mm)] (3) Drop bag breakage rate Kyoei Co., Ltd. PP-500 type For fusion cutting sealer equipped with fusing blade for OPP film The fusing seal temperature 38
Bag size 250 x 30 under conditions of 0 ℃ and bag making speed of 80 sheets / min
A 0 mm bag was produced. 1 kg of potatoes was placed in this bag and naturally dropped on the floor from a height of 0.75 m. The floor was made of PVC tile manufactured by Toyo Rinorum Co., Ltd. As the evaluation method, the same bag was dropped up to 15 times, and the number of drops until the bag was broken was measured. The number of tests was set to 10 and the bag breakage rate was calculated by the following formula.

【0026】破袋率(%)=〔15−破袋までの落下回
数〕÷15×100 なお、OPPフィルムの場合は最適の強度が得られるよ
う溶断シール温度を400℃に、CPPフィルムの場合
は同様に溶断シール温度を230℃に変更した以外は同
条件とした。
Bag breakage rate (%) = [15-number of drops until bag breakage] ÷ 15 × 100 In the case of OPP film, the fusing seal temperature is 400 ° C. and in the case of CPP film, the optimum strength is obtained. Similarly, the same conditions were used except that the fusing seal temperature was changed to 230 ° C.

【0027】(4)製袋作業性 共栄株式会社製PP−500型製袋機において、溶断シ
ール温度380℃、製袋速度120枚/分の条件で袋寸
法(W×L)250×300mmを連続製袋した。この
作業を熟練した人が一人で作業した時、製袋された袋1
00枚をきれいに揃え作業を行う際、次の100枚が製
袋されるまでに、袋の揃えが完了する場合を○とし、完
了しない時を×とした。
(4) Bag-making workability In a PP-500 type bag-making machine manufactured by Kyoei Co., Ltd., bag dimensions (W × L) of 250 × 300 mm were obtained under the conditions of fusing seal temperature of 380 ° C. and bag-making speed of 120 sheets / min. Continuous bag making. A bag 1 made by a person skilled in this work
When the 00 pieces are neatly aligned, the case where the bag alignment is completed by the time the next 100 sheets are manufactured is marked with ◯, and the case where the bag alignment is not completed is marked with x.

【0028】実施例1 エチレン含有量2.2重量%、メルトインデックス2.
2g/10分のエチレン−プロピレン共重合体100重
量部に、酸化防止剤(BHT)として0.2重量部、帯
電防止剤としてグリセリンモノステアレートとN,N´
−ビス(2−ヒドロキシエチル)ステアリルアミンを夫
々0.1重量部、エルカ酸アミド0.01重量部、ステ
アリン酸カルシウム0.04重量部、平均粒子径2μの
シリコーンゴム微粒子0.1重量部を加えて溶融混練
し、二軸延伸フィルム用原料とした。この原料をTダイ
型押出機を用いて260℃で溶融押出し、40℃のキャ
スティングロール上で1.35mmのシートとした。こ
のシートを125℃の加熱ロールにて予熱し縦方向に
3.5倍延伸した。次いで、145℃に加熱された横延
伸機内で横方向に9倍に延伸後、横延伸機の熱セットゾ
ーンで150℃にて7%横方向にリラックスさせた。得
られたフィルムの厚さは40μmであった。こうして得
られたフィルムの強度、伸び率、引張り弾性率、および
溶断シール機にて製袋した袋の製袋作業性および落下破
袋テストの結果を表1に示した。
Example 1 Ethylene content 2.2% by weight, melt index 2.
100 parts by weight of an ethylene-propylene copolymer of 2 g / 10 minutes, 0.2 parts by weight as an antioxidant (BHT), glycerin monostearate and N, N 'as an antistatic agent.
0.1 parts by weight of bis (2-hydroxyethyl) stearylamine, 0.01 parts by weight of erucic acid amide, 0.04 parts by weight of calcium stearate, and 0.1 parts by weight of silicone rubber fine particles having an average particle diameter of 2 μ were added. And melt-kneaded to obtain a raw material for a biaxially stretched film. This raw material was melt-extruded at 260 ° C. using a T-die type extruder, and a 1.35 mm sheet was formed on a casting roll at 40 ° C. This sheet was preheated with a heating roll at 125 ° C. and stretched 3.5 times in the machine direction. Then, the film was stretched 9 times in the transverse direction in a transverse stretching machine heated to 145 ° C., and then relaxed in the transverse direction by 7% at 150 ° C. in a heat setting zone of the transverse stretching machine. The thickness of the obtained film was 40 μm. Table 1 shows the strength, elongation, tensile modulus of elasticity of the film thus obtained, and the bag-making workability and bag-breaking test result of the bag made by the fusing and sealing machine.

【0029】実施例2 エチレン含有量1.3重量%、ブテン−1含有量7.0
重量%、メルトインデックス5.0g/10分のエチレ
ン−ブテン−1−プロピレン共重合体100重量部に、
実施例1と同様の添加剤配合を行った樹脂を同じくTダ
イ型押出機を用いて240℃で溶融押出し、30℃のキ
ャスティングロール上で1.02mmのシートとした以
外は実施例1と同様条件にて二軸延伸を行った。得られ
たフィルムの厚さは30μmであった。こうして得られ
たフィルムの性能評価を実施例1と同様に行い、結果を
表1に示した。
Example 2 Ethylene content 1.3% by weight, butene-1 content 7.0
% By weight and 100 parts by weight of ethylene-butene-1-propylene copolymer having a melt index of 5.0 g / 10 min.
Same as Example 1 except that the resin containing the same additives as in Example 1 was melt extruded at 240 ° C. using the same T-die type extruder to form a sheet of 1.02 mm on a casting roll at 30 ° C. Biaxial stretching was performed under the conditions. The thickness of the obtained film was 30 μm. The performance of the film thus obtained was evaluated in the same manner as in Example 1, and the results are shown in Table 1.

【0030】実施例3 エチレン含有量2.5重量%、メルトインデックス6.
0g/10分のエチレン−プロピレン共重合体80重量
部とメルトインデックス2.0g/10分のプロピレン
単独重合体20重量部に実施例1と同様の添加剤を配合
した混合物を同じくTダイ型押出機を用いて250℃で
溶融押出し、35℃のキャスティングロール上で1.3
5mmのシートとした以外は実施例1と同様の条件にて
二軸延伸を行った。得られたフィルムの厚さは40μm
であった。こうして得られたフィルムの性能評価を実施
例1と同様に行い、結果を表1に示した。
Example 3 Ethylene content 2.5% by weight, melt index 6.
A mixture of 80 parts by weight of an ethylene-propylene copolymer at 0 g / 10 minutes and 20 parts by weight of a propylene homopolymer at a melt index of 2.0 g / 10 minutes with the same additives as in Example 1 was also subjected to T-die type extrusion. Melt extruding at 250 ° C using a machine and 1.3 on a casting roll at 35 ° C.
Biaxial stretching was performed under the same conditions as in Example 1 except that a 5 mm sheet was used. The thickness of the obtained film is 40 μm
Met. The performance of the film thus obtained was evaluated in the same manner as in Example 1, and the results are shown in Table 1.

【0031】実施例4 エチレン含有量2.2重量%、メルトインデックス2.
2g/10分のエチレン−プロピレン共重合体70重量
部とエチレン含有量1.3重量%、ブテン−1含有量
7.0重量%、メルトインデックス5.0g/10分の
エチレン−ブテン−1−プロピレン共重合体30重量部
に実施例1と同様の添加剤を配合した混合物を同じくT
ダイ型押出機を用いて260℃で溶融押出し、40℃の
キャスティングロール上で1.35mmのシートとした
以外は実施例1と同様条件にて二軸延伸を行った。得ら
れたフィルムの厚さは40μmであった。こうして得ら
れたフィルムの性能評価を実施例1と同様に行い、結果
を表1に示した。
Example 4 Ethylene content 2.2% by weight, melt index 2.
70 parts by weight of an ethylene-propylene copolymer at 2 g / 10 minutes, an ethylene content of 1.3% by weight, a butene-1 content of 7.0% by weight, and a melt index of 5.0 g / 10 minutes of ethylene-butene-1-. A mixture of 30 parts by weight of the propylene copolymer and the same additives as in Example 1 was mixed with T
Biaxial stretching was performed under the same conditions as in Example 1 except that melt extrusion was performed at 260 ° C. using a die-type extruder, and a 1.35 mm sheet was formed on a casting roll at 40 ° C. The thickness of the obtained film was 40 μm. The performance of the film thus obtained was evaluated in the same manner as in Example 1, and the results are shown in Table 1.

【0032】比較例1 メルトインデックス2.0g/10分のプロピレン単独
重合体100重量部に帯電防止剤を1.0重量部に増し
た以外は実施例1と同様の添加剤を配合し、同じくTダ
イ型押出機を用いて280℃で溶融押出し、35℃のキ
ャスティングロール上で1.35mmのシートとした以
外は実施例1と同様条件にて二軸延伸を行った。しか
し、得られたフィルムは縦延伸倍率が不足のため、MD
方向の厚みが30〜120μmと大きくバラツクととも
に部分的にまだら状の未延伸部分が混入しており、実用
に共し得るフィルムが得られなかった。
Comparative Example 1 The same additives as in Example 1 were blended except that 100 parts by weight of a propylene homopolymer having a melt index of 2.0 g / 10 min was added with 1.0 part by weight of an antistatic agent, and Biaxial stretching was performed under the same conditions as in Example 1 except that melt extrusion was performed at 280 ° C. using a T-die type extruder and a 1.35 mm sheet was formed on a casting roll at 35 ° C. However, since the obtained film has insufficient longitudinal stretching ratio, MD
The thickness in the direction was as large as 30 to 120 μm, and unevenness was partially mixed in a mottled area, and a film that could be used practically was not obtained.

【0033】比較例2 比較例1と同様の樹脂を二軸延伸において縦延伸倍率5
00%に延伸した以外は実施例1と同様に行った。得ら
れたフィルムの厚さは40μmであった。こうして得ら
れたフィルムの性能評価を実施例1と同様に行い、結果
を表1に示した。
Comparative Example 2 A resin similar to that of Comparative Example 1 was biaxially stretched in a longitudinal stretching ratio of 5
The same procedure as in Example 1 was performed except that the film was stretched to 00%. The thickness of the obtained film was 40 μm. The performance of the film thus obtained was evaluated in the same manner as in Example 1, and the results are shown in Table 1.

【0034】比較例3 エチレン含有量1.3重量%、ブテン−1含有量7.0
重量%、メルトインデックス5.0g/10分のエチレ
ン−ブテン−1−プロピレン共重合体100重量部に実
施例1と同様の添加剤を配合し、同じくTダイ型押出機
を用いて210℃で溶融押出し、30℃のキャスティン
グロール上で40μmの無延伸フィルムを得た。こうし
て得られたフィルムの性能評価を実施例1と同様に行
い、結果を表1に示した。
Comparative Example 3 Ethylene content 1.3% by weight, butene-1 content 7.0
% Of ethylene-butene-1-propylene copolymer having a melt index of 5.0 g / 10 min and the same additives as in Example 1 were blended, and the same T-die type extruder was used at 210 ° C. Melt extrusion was carried out to obtain a 40 μm unstretched film on a casting roll at 30 ° C. The performance of the film thus obtained was evaluated in the same manner as in Example 1, and the results are shown in Table 1.

【0035】比較例4 特公平5−82416号公報の実施例1に記載されたブ
テン−1含有量26.5モル%のプロピレン−ブテン−
1ランダム共重合体50重量%とエチレン含有量5.8
モル%のプロピレン−エチレンランダム共重合体50重
量%との混合物をTダイ型押出機を用いて230℃で溶
融押出し、40℃のキャスティングロール上で1.35
mmのシートとした。このシートを120℃の加熱ロー
ルにて予熱し縦方向に3倍延伸した。次いで、120℃
に加熱された横延伸機内で横方向に3倍に延伸後、横延
伸機の熱セットゾーンで120℃にて7%横方向にリラ
ックスさせた。得られたフィルムの厚さは40μmであ
った。このフィルムの性能評価を実施例1と同様に行
い、結果を表1に示した。
Comparative Example 4 Propylene-butene-containing 26.5 mol% butene-1 described in Example 1 of JP-B-5-82416.
50% by weight of random copolymer and ethylene content of 5.8
A mixture with 50% by weight of propylene-ethylene random copolymer of mol% was melt extruded using a T-die type extruder at 230 ° C. and 1.35 on a casting roll at 40 ° C.
mm sheet. This sheet was preheated with a heating roll at 120 ° C. and stretched 3 times in the machine direction. Then 120 ° C
After being stretched 3 times in the transverse direction in the transverse stretching machine heated to 1, it was relaxed in the transverse direction by 7% at 120 ° C. in the heat setting zone of the transverse stretching machine. The thickness of the obtained film was 40 μm. The performance of this film was evaluated in the same manner as in Example 1, and the results are shown in Table 1.

【0036】[0036]

【表1】 [Table 1]

フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 B29L 7:00 Continuation of front page (51) Int.Cl. 6 Identification number Office reference number FI technical display area B29L 7:00

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】エチレン含有量が1〜4重量%のエチレン
−プロピレン共重合体、または、エチレン含有量0.5
〜3.0重量%且つブテン−1含有量4〜15重量%の
エチレン−ブテン−プロピレン共重合体からなり、MD
方向の引張強度5kg/mm2における伸び率が30〜
150%であり、MD方向の引張弾性率が80〜130
kg/mm2であることを特徴とする二軸延伸ポリオレ
フィンフィルム。
1. An ethylene-propylene copolymer having an ethylene content of 1 to 4% by weight, or an ethylene content of 0.5.
-3.0 wt% and butene-1 content 4-15 wt% ethylene-butene-propylene copolymer, MD
Direction tensile strength 5kg / mm 2 elongation of 30 ~
It is 150% and the tensile elastic modulus in the MD direction is 80 to 130.
A biaxially stretched polyolefin film, characterized in that it is kg / mm 2 .
JP3329194A 1994-03-03 1994-03-03 Biaxially oriented polyolefin film Pending JPH07241906A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3329194A JPH07241906A (en) 1994-03-03 1994-03-03 Biaxially oriented polyolefin film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3329194A JPH07241906A (en) 1994-03-03 1994-03-03 Biaxially oriented polyolefin film

Publications (1)

Publication Number Publication Date
JPH07241906A true JPH07241906A (en) 1995-09-19

Family

ID=12382441

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3329194A Pending JPH07241906A (en) 1994-03-03 1994-03-03 Biaxially oriented polyolefin film

Country Status (1)

Country Link
JP (1) JPH07241906A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6294632B1 (en) 1996-07-24 2001-09-25 Chisso Corporation Biaxially oriented polypropylene film
US6395071B1 (en) 1999-10-01 2002-05-28 Chisso Corporation Breathing film
EP1209187A1 (en) * 2000-11-28 2002-05-29 Borealis GmbH Use of propylene terpolymers for the production of films
WO2002044251A1 (en) * 2000-11-28 2002-06-06 Borealis Gmbh Use of propylene terpolymers for the production of films
US6716921B1 (en) 1999-09-07 2004-04-06 Chisso Corporation Propylene resin composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6294632B1 (en) 1996-07-24 2001-09-25 Chisso Corporation Biaxially oriented polypropylene film
US6716921B1 (en) 1999-09-07 2004-04-06 Chisso Corporation Propylene resin composition
US6395071B1 (en) 1999-10-01 2002-05-28 Chisso Corporation Breathing film
EP1209187A1 (en) * 2000-11-28 2002-05-29 Borealis GmbH Use of propylene terpolymers for the production of films
WO2002044251A1 (en) * 2000-11-28 2002-06-06 Borealis Gmbh Use of propylene terpolymers for the production of films
WO2002044252A1 (en) * 2000-11-28 2002-06-06 Borealis Gmbh Use of propylene terpolymers for the production of films

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