JPS6343932A - Production of biaxially oriented gas-permeable film - Google Patents

Production of biaxially oriented gas-permeable film

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Publication number
JPS6343932A
JPS6343932A JP18811086A JP18811086A JPS6343932A JP S6343932 A JPS6343932 A JP S6343932A JP 18811086 A JP18811086 A JP 18811086A JP 18811086 A JP18811086 A JP 18811086A JP S6343932 A JPS6343932 A JP S6343932A
Authority
JP
Japan
Prior art keywords
film
stretching
polyolefin resin
temperature
inorganic filler
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
JP18811086A
Other languages
Japanese (ja)
Inventor
Kuniji Hashimoto
橋本 城次
Hideki Hattori
英樹 服部
Mitsuaki Yamahara
山原 三昭
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Petrochemical Co Ltd
Original Assignee
Mitsubishi Petrochemical 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 Mitsubishi Petrochemical Co Ltd filed Critical Mitsubishi Petrochemical Co Ltd
Priority to JP18811086A priority Critical patent/JPS6343932A/en
Publication of JPS6343932A publication Critical patent/JPS6343932A/en
Pending legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)

Abstract

PURPOSE:To produce the title highly gas-permeable film, by biaxially orienting a film comprising a composition containing a polyolefin resin and an inorganic filler and orienting the obtained film in the machine direction. CONSTITUTION:A composition is obtained by mixing 42-87vol% polyolefin resin (e.g., ethylene/proplene copolymer) of a density of 0.910-0.940g/cm<3> and an MFR of 0.1-5g/10min with 58-13vol% inorganic filler (e.g., CaCO3) of an average particle diameter of 0.1-5mum and, optionally, a softener, a dispersant, a heat stabilizer, etc. This composition is molded into a film, which is biaxially oriented consecutively at a ratio of 1.2-12 for each direction in a temperature range lower than the m.p. of the resin by 80-20 deg.C. The obtained film is oriented in the machine direction at a ratio of 1.1-5 in a temperature range lower than the m.p. of the resin by 100-25 deg.C to obtain a gas-permeable oriented film of a thickness of 25-150mu and a moisture permeability (JIS Z-0208) of 300-25,000g/cm<2>.24hr.

Description

【発明の詳細な説明】 (<産業上の利用分野 本発明は、ポリオレフィン系樹脂と無機充填剤との組成
物からなるフィルムを二軸延伸することよりなる通気性
フィルムの製造方法に関し、特に、紙おむつ、あるいは
生理用品等の衛生用品への利用に適する、高度の通気性
を有する通気性フィルムの製造方法に関する。
Detailed Description of the Invention (<Industrial Field of Application) The present invention relates to a method for producing a breathable film by biaxially stretching a film made of a composition of a polyolefin resin and an inorganic filler. The present invention relates to a method for producing a breathable film having a high degree of breathability and suitable for use in sanitary products such as disposable diapers or sanitary products.

(ロ)従来の技術 従来より、ポリオレフィン系樹脂と無機充填剤との組成
物からなるフィルムを一軸あるいは二軸方向に延伸して
、フィルムに連通したボイドを発生させて通気性フィル
ムを製造する方法は多数提案されており、この通気性フ
ィルムは、紙おむつ、あるいは生理用品等の衛生用品等
用途への応用が試みられ始めている。
(B) Conventional technology Conventionally, a method of manufacturing a breathable film by stretching a film made of a composition of a polyolefin resin and an inorganic filler in uniaxial or biaxial directions to generate voids that communicate with the film. A number of proposals have been made, and attempts are being made to apply this breathable film to sanitary products such as disposable diapers and sanitary products.

しかしながら、−軸延伸法による通気性フィルムは、機
械的強度面での方向性が大きいという問題、特に、延伸
方向に裂は易いという問題、があし、一方、二軸延伸法
による通気性フィルムは、−軸延伸法におけるその方向
性の問題は解消されているものの、通気性が、予想され
る程の値を示さないばかりか、むしろ−軸延伸法による
通気性フィルムよ9劣るという問題がある。
However, the breathable film produced by the biaxial stretching method has the problem of large directional properties in terms of mechanical strength, especially the problem of easy tearing in the direction of stretching.On the other hand, the breathable film produced by the biaxial stretching method Although the problem of the directionality in the -axial stretching method has been resolved, there is a problem that the breathability not only does not show the expected value, but is actually inferior to the breathable film produced by the -axial stretching method. .

(ハ)発明が解決しようとする問題点 以上のように、ポリオレフィン系樹脂と無機充填剤との
組成物からなるフィルムを二軸延伸して通気性フィルム
を製造する従来の方法では、高度の通気性を有する通気
性フィルムを製造するには到っていないのが現状であり
、本発明は、この現状に鑑み、従来の製造方法における
問題点を解決することを目的としてなされたものである
(c) Problems to be Solved by the Invention As mentioned above, the conventional method of producing a breathable film by biaxially stretching a film made of a composition of a polyolefin resin and an inorganic filler has a high degree of air permeability. At present, it has not yet been possible to produce a breathable film that has good properties, and in view of this current situation, the present invention was made with the aim of solving the problems in conventional manufacturing methods.

に)問題点を解決するための手段 本発明の二軸延伸通気性フィルムの製造方法は、ポリオ
レフィン系樹脂42〜87体積%と無機充填剤58〜1
3体積5との組成物からなるフィルムを、同時または逐
次に、縦方向と横方向に二軸延伸した後、該ポリオレフ
ィン系樹脂の融点より100℃から25℃低い範囲の温
度で、さらに縦方向に延伸することを特徴とする。
B) Means for Solving the Problems The method for producing a biaxially stretched breathable film of the present invention comprises a polyolefin resin of 42 to 87% by volume and an inorganic filler of 58 to 1% by volume.
After a film consisting of a composition with a volume of 3 and 5 is biaxially stretched in the machine direction and the transverse direction simultaneously or sequentially, it is further stretched in the machine direction at a temperature in the range of 100 to 25 °C lower than the melting point of the polyolefin resin. It is characterized by stretching.

ここで、ポリオレフィン系樹脂とは、低密度ポリエチレ
ン、高密度ポリエチレン、ポリプロピレン等の如き重合
体、エチレン−プロピレン共重合体、エチレン−ブテン
−1共重合体等の如きエチレン−α−オレフィン共重合
体等をいい、これらは、単独で、あるいは混合状態で用
いることができる。これらの中でも特にエチレン−α−
オレフィン共重合体が、通気性フィルムにソフト感を付
与する上で好ましく、就中、密度が0.910〜0.9
40 f/cd、好ましくは0.916〜0.935 
t/adで、MFRが0.1〜s t/x o分、好ま
しくは0.1〜3 t/x o分の範囲に含まれるもの
がよい。エチレン−α−オレフィン共重合体の密度が0
.910 tlad未溝になるとフィルムの均一延伸が
困難となり、0.940 f/adを越えると通気性フ
ィルムにソフト感を付与することが困難となる。また、
MFRが0.1f/10分未満になるとフィルムをグイ
間隙より溶融押出しする際、異常流動が発生し均一なフ
ィルムが得られなくなり、st/10分を越えると均一
延伸が困難となる。
Here, the polyolefin resin refers to polymers such as low density polyethylene, high density polyethylene, polypropylene, etc., and ethylene-α-olefin copolymers such as ethylene-propylene copolymer, ethylene-butene-1 copolymer, etc. etc., and these can be used alone or in a mixed state. Among these, ethylene-α-
Olefin copolymers are preferred in terms of imparting a soft feel to the breathable film, especially those with a density of 0.910 to 0.9.
40 f/cd, preferably 0.916-0.935
t/ad, the MFR is preferably in the range of 0.1 to s t/xo minutes, preferably 0.1 to 3 t/xo minutes. Density of ethylene-α-olefin copolymer is 0
.. If it is 910 tlad without grooves, it will be difficult to stretch the film uniformly, and if it exceeds 0.940 f/ad, it will be difficult to impart a soft feel to the breathable film. Also,
If the MFR is less than 0.1 f/10 minutes, abnormal flow occurs when the film is melt-extruded through the goo gap, making it impossible to obtain a uniform film, and if it exceeds st/10 minutes, uniform stretching becomes difficult.

なお、ここで、エチレン−α−オレフィン共重合体とは
、C3〜C8の分子骨格であるα−オレフィンが1〜2
0重量よ、好ましくは3〜15重t%、エチレンが99
〜80重量%、好ましくは97〜85重量%からなる直
鎖状低密度エチレン共重合体で、遷移金属化合物と有機
金属化合物とを組合せた触媒を用いてイオン反応により
エチレンとC3〜Csの分子骨格であるα−オレフィン
を1つ以上含んで共重合させて生成される樹脂でアや、
一般的に知られている酸素ラジカルを開始剤とし高圧力
下でラジカル反応によりエチレンを重合させて生成され
る分岐状低密度ポリエチレン樹脂とは、分子構造、溶融
特性、結晶化特性、固体物性、延伸特性において異なっ
た性能を有するものである。
In addition, here, the ethylene-α-olefin copolymer refers to 1 to 2 α-olefins having a C3 to C8 molecular skeleton.
0% by weight, preferably 3 to 15% by weight, 99% by weight of ethylene
A linear low-density ethylene copolymer consisting of ~80% by weight, preferably 97-85% by weight, in which ethylene and C3 to Cs molecules are reacted by ionic reaction using a catalyst containing a combination of a transition metal compound and an organometallic compound. A resin produced by copolymerization containing one or more α-olefins as a backbone.
Branched low-density polyethylene resin, which is produced by polymerizing ethylene through a radical reaction under high pressure using commonly known oxygen radicals as an initiator, is characterized by its molecular structure, melting characteristics, crystallization characteristics, solid physical properties, They have different performance in stretching properties.

また、無機充填剤は、炭酸カルシウム、酸化カルシウム
、タルク、クレー、シリカ、酸化チタン、アルミナ、硫
酸アルミニウム等であり、単独あるいは混合状態で用い
ることができる。
Inorganic fillers include calcium carbonate, calcium oxide, talc, clay, silica, titanium oxide, alumina, aluminum sulfate, etc., and can be used alone or in a mixed state.

好ましい無機充填剤の形態としては、板状、棒状、針状
以外の球状、粒状、不定形等であり、その平均粒径は0
.1〜51’s好ましくは0.6〜3μである。平均粒
径が0.1μ未満になるとフィルムの延伸時の伸びがな
くなって延伸が困難にな抄、5μを越えると延伸フィル
ムの表面の凹凸が荒くなり通気性フィルムとして望まし
くなくなるとともに、60μ以下の薄いフィルムを製造
するにおいて連続安定延呻性が損われる。
Preferred forms of the inorganic filler are plate-like, rod-like, spherical other than needle-like, granular, amorphous, etc., and the average particle size is 0.
.. 1 to 51's, preferably 0.6 to 3μ. If the average particle size is less than 0.1μ, the film loses its elongation during stretching, making it difficult to stretch.If it exceeds 5μ, the surface of the stretched film becomes rough, making it undesirable as a breathable film. Continuous stable stretchability is impaired in producing thin films.

ポリオレフィン系樹脂と無機充填剤との組成比は、ポリ
オレフィン系樹脂が42〜87体積%、好ましくFi5
5〜80体積%、無機充填剤が58〜13体積%、好ま
しくは45〜20体積%の範囲である。無機充填剤が1
3体積%未溝になると、ポリオレフィン系樹脂と無機充
填剤との界面が剥離してできる隣接したボンドどうしが
連通しなくな抄、通気性が得られなくなる。また、58
体積%を越えると、フィルムの延伸時の伸びがなくな9
、延伸が困難になる。
The composition ratio of the polyolefin resin and the inorganic filler is 42 to 87% by volume of the polyolefin resin, preferably Fi5
The content of the inorganic filler is 58-13% by volume, preferably 45-20% by volume. 1 inorganic filler
When 3% by volume of the groove is left ungrooved, the interface between the polyolefin resin and the inorganic filler peels off, and adjacent bonds are no longer in communication with each other, making it impossible to obtain papermaking and air permeability. Also, 58
If the volume% is exceeded, the film will not elongate during stretching.9
, stretching becomes difficult.

ポリオレフィン系樹脂と無機充填剤とは、必要に応じて
、脂肪族アルコール系指切酸エステル、低分子量炭化水
素重合体等の軟化剤、および、通常用いられる分散剤、
熱安定剤、紫外線吸収剤、滑剤、顔料、帯電防止剤等を
嘔らに添加して、−軸あるいは二軸押出機、バンバIJ
−ミキサー、ニーダ−、ミキシングロール等ニよつて加
熱混練することによ抄組成物とした後、公知のTダイ成
形、インフレーション成形等でフィルムとする。
The polyolefin resin and the inorganic filler are, if necessary, a softening agent such as an aliphatic alcohol-based ester, a low molecular weight hydrocarbon polymer, and a commonly used dispersing agent.
Heat stabilizers, ultraviolet absorbers, lubricants, pigments, antistatic agents, etc. are added to the core, and the extrusion process is carried out using a -screw or twin-screw extruder, Bamba IJ.
The composition is heated and kneaded using a mixer, kneader, mixing roll, etc. to form a paper composition, and then formed into a film by known T-die molding, inflation molding, etc.

本発明においては、このフィルムを、同時または逐次に
縦方向と横方向に二軸延伸した後、さらに縦方向に延伸
するう この後段階の縦方向延伸を実施しない場合には、高度の
通気性を有する延伸フィルムが得られないこととなる。
In the present invention, the film is biaxially stretched in the machine direction and the transverse direction simultaneously or sequentially, and then further stretched in the machine direction.If the film is not subjected to the post-stretch process in the machine direction, the film has a high degree of air permeability. Therefore, a stretched film having the following properties cannot be obtained.

ここで、前段階の二軸延伸法としては公知の方法でよく
、具体的には、例えば、ロールで縦方向に延伸し、次い
でテンターで横方向に延伸する方法、チューブ状で縦方
向に延伸し、次いで横方向に延伸する方法等の逐次二軸
延伸法、テンターで縦方向と横力向に同時に延伸する方
法、チューブ状で縦方向と横方向に同時に延伸する方法
等の同時二軸延伸法等が挙げられる。
Here, the biaxial stretching method in the previous stage may be a known method, and specifically, for example, a method of stretching in the longitudinal direction with a roll and then stretching in the transverse direction with a tenter, a method of stretching in the longitudinal direction with a tube shape, etc. simultaneous biaxial stretching, such as a method in which a tenter is used to simultaneously stretch the longitudinal direction and the lateral force direction; and a method in which a tubular shape is simultaneously stretched in the longitudinal and transverse directions. Laws etc.

なお、この際、逐次二軸延伸法における縦方向延伸温度
は、通常、用いたポリオレフィン系樹脂の融点より80
℃から20℃低い範囲の温度、横方向延伸温度はその融
点より40℃から0℃低い範囲の温度であり、同時二軸
延伸法における延伸温度は、通常、その融点より80℃
から10℃低い範囲の温度である。また、睡伸倍率は、
縦方向および横方向とも各々1.2〜12倍、好ましく
は1.2〜10倍である。
At this time, the longitudinal stretching temperature in the sequential biaxial stretching method is usually 80° below the melting point of the polyolefin resin used.
℃ to 20℃ lower, the transverse stretching temperature is 40℃ to 0℃ lower than the melting point, and the stretching temperature in the simultaneous biaxial stretching method is usually 80℃ lower than the melting point.
The temperature range is 10°C lower than the average temperature. In addition, the sleep stretch magnification is
It is 1.2 to 12 times, preferably 1.2 to 10 times in both the vertical and horizontal directions.

また、後段階の縦延伸法も公知の方法、具体的には、例
えば、ロール、テンターでの延伸法、およびチューブ状
での延伸法等を用いることができる。この際の延伸温度
は、用いたポリオレフィン系樹脂の融点より100℃か
ら25℃低い範囲の温度とすることが必須であり、好ま
しくは90℃から30℃低い範囲、特に好ましくは85
℃から40℃低い範囲の温度とする。また、延伸倍率は
1.1〜5倍とする。
Further, the longitudinal stretching method in the later stage can also be a known method, specifically, for example, a stretching method using a roll or a tenter, a stretching method using a tube shape, or the like. It is essential that the stretching temperature at this time be in the range of 100°C to 25°C lower than the melting point of the polyolefin resin used, preferably in the range of 90°C to 30°C lower, particularly preferably 85°C.
The temperature should be in the range of 40°C lower than ℃. Further, the stretching ratio is 1.1 to 5 times.

この延伸温度が、前記の下限篇度より低い場合には延伸
することが困難となり、一方、前記の上限温度より高い
場合には、高度の通気性を有する延伸フィルムが得られ
ないこととなる。
If the stretching temperature is lower than the lower limit, it will be difficult to stretch, while if it is higher than the upper limit, a stretched film with high air permeability will not be obtained.

なお、延伸したフィルムの寸法精度を安定化させるため
、通常は、延伸後に熱処理する。
Note that in order to stabilize the dimensional accuracy of the stretched film, it is usually heat-treated after stretching.

本発明によって製造される二軸延伸通気性フィルムの物
性は、ポリオレフィン系樹脂の種頭、物性、無機充填剤
の種類、粒径、充填割合、延伸条件である延伸温度、延
伸倍率等により自由にコントロール可能である。通気性
フィルムの厚みが25〜150μの場合、J工S zO
208で測定した透湿度は300〜25000?/m1
・24時間の範囲の値を有するのが望ましく、厚みは、
60μ以下が好ましく、特には50μ以下が好ましい。
The physical properties of the biaxially stretched breathable film produced according to the present invention can be freely controlled depending on the seed head of the polyolefin resin, the physical properties, the type of inorganic filler, the particle size, the filling ratio, the stretching conditions such as the stretching temperature, the stretching ratio, etc. It is controllable. When the thickness of the breathable film is 25 to 150μ, J Engineering SzO
The moisture permeability measured with 208 is 300 to 25,000? /m1
・It is desirable to have a value in the range of 24 hours, and the thickness is
The thickness is preferably 60μ or less, particularly preferably 50μ or less.

(ホ)作用 本発明の二軸延伸通気性フィルムの製造方法は、縦方向
と横方向に二軸延伸した後、さらに、特定範囲の温度で
縦方向に延伸するので、高度の通気性を有する通気性フ
ィルムが製造できるものである。
(E) Function The method for producing a biaxially stretched breathable film of the present invention involves biaxially stretching in the longitudinal and transverse directions, and then further stretching in the longitudinal direction at a temperature within a specific range, so that it has a high degree of breathability. A breathable film can be produced.

なお、この後段階の縦方向延伸は、前段階の二軸延伸に
おける横方向延伸の温度を延伸安定化のために樹脂の軟
化点以上で融点近傍までという高い@度とすることに起
因する延伸フィルム表面の軟化もしくは溶融によるボイ
ドの閉塞を、開放するという作用を有するものと考えら
れる。
In addition, the longitudinal stretching in this latter stage is a stretching process caused by setting the temperature of the transverse stretching in the biaxial stretching in the previous stage to a high degree of at least the softening point of the resin and close to the melting point in order to stabilize the stretching. It is thought that it has the effect of releasing voids that are blocked due to softening or melting of the film surface.

(へ)実施例 実施例1 エチレン−ブテン−1共重合体(ブテン−1含量6重量
%、密度0.923 r/、:+(、MFRo、9f/
10分、融点124℃)のパウダー65体積%、重質炭
酸カルシウム(平均粒径1.2μ、板状棒状でない不定
形)35体積%、エチレン−ブテン−1共重合体100
重量部に対して熱安定剤(2,6−ジーt−ブチル−p
−クレゾール)0.1重量部、重質炭酸カルシウム10
0重量部に対して分散剤(オレイン酸)1.0重量部、
およびこれらの合計11100重量部に対して精製ヒマ
シ油(グリセリントリリンル−ト85%以上含有、伊藤
製油社製)5重な部をスーパーミキサーで5分間混合し
た後、二軸押出機より200℃でストランド状に押出し
た後、ペレット状に切断した。
(to) Examples Example 1 Ethylene-butene-1 copolymer (butene-1 content 6% by weight, density 0.923 r/, :+(, MFRo, 9f/
10 minutes, melting point 124°C) powder 65% by volume, heavy calcium carbonate (average particle size 1.2μ, irregular shape, not plate-shaped or rod-like) 35% by volume, ethylene-butene-1 copolymer 100%
Heat stabilizer (2,6-di-tert-butyl-p
-cresol) 0.1 part by weight, heavy calcium carbonate 10
1.0 parts by weight of dispersant (oleic acid) per 0 parts by weight,
A total of 11,100 parts by weight of these was mixed with 5 parts of refined castor oil (containing 85% or more of glycerin triline root, manufactured by Ito Oil Co., Ltd.) in a super mixer for 5 minutes, and then heated at 200°C in a twin-screw extruder. After extruding it into a strand, it was cut into pellets.

得られたペレットを、スクリュー径50e1L/D 2
5の押出機に取り付けたTダイよ抄210℃で押出した
後、25℃の表面温度の冷却ロールにて冷却固化して厚
み60μのフィルムとした。
The obtained pellets were mixed with a screw diameter of 50e1L/D2
After extruding through a T-die attached to the extruder No. 5 at 210° C., the mixture was cooled and solidified using a cooling roll with a surface temperature of 25° C. to form a film with a thickness of 60 μm.

このフィルムを、ロール延伸法により、延伸温度70℃
、延伸倍率1.2倍で縦方向に延伸し、次いで、テンタ
ー法により、延伸温度110℃、延伸倍率2倍で横方向
に延伸した。その後、さらに、ロール延伸法により、延
伸温度60℃、延伸倍率1.4倍で縦方向に延伸するこ
とによ抄、厚+40μの通気性フィルムを製造した。
This film was stretched at a temperature of 70°C by a roll stretching method.
The film was stretched in the machine direction at a stretching ratio of 1.2 times, and then stretched in the transverse direction at a stretching temperature of 110° C. and a stretching ratio of 2 times by a tenter method. Thereafter, the film was further stretched in the longitudinal direction by a roll stretching method at a stretching temperature of 60° C. and a stretching ratio of 1.4 times to produce a breathable film having a thickness of +40 μm.

得られた通気性フィルムについて、J工521702に
基づいて測定した引裂強度、シよび、J工S z020
8に基づいて測定した透湿度を表1に示す。
Regarding the obtained breathable film, the tear strength measured based on J Engineering 521702, and J Engineering S z020
Table 1 shows the moisture permeability measured based on No. 8.

実施例2 実施例1における後段階の縦方向延伸温度を80℃とし
た外は、実施例1と同様にして通気性フィルムを製造し
た。
Example 2 A breathable film was produced in the same manner as in Example 1, except that the longitudinal stretching temperature in the latter stage was 80°C.

得られた通気性フィルムの引裂強度および透湿度の測定
結果を表1に示す。
Table 1 shows the measurement results of the tear strength and moisture permeability of the breathable film obtained.

比較例1 実施例1と同様の方法によ抄得られた未延伸フィルムを
、ロール延伸法により、延伸温度60℃、延伸倍率2倍
で縦方向に延伸することにより一軸延伸フィルムを製造
した。
Comparative Example 1 A uniaxially stretched film was produced by stretching an unstretched film obtained by the same method as in Example 1 in the longitudinal direction using a roll stretching method at a stretching temperature of 60° C. and a stretching ratio of 2 times.

得られた一軸延伸フイルムの引裂強度および透湿度の測
定結果を表1に示す。
Table 1 shows the measurement results of the tear strength and moisture permeability of the obtained uniaxially stretched film.

比較例2 実施例1と同様の方法により得られた未延伸フィルムを
、ロール延伸法によ抄、延伸温度60℃、延伸倍率1.
5倍で縦方向に延伸し、次いで、テンター法により、延
伸温度110℃、延伸倍率2倍で横方向に延伸すること
によや二軸延伸フィルムを製造した。
Comparative Example 2 An unstretched film obtained by the same method as in Example 1 was subjected to paper-stretching using a roll stretching method, at a stretching temperature of 60°C and a stretching ratio of 1.
A semi-biaxially stretched film was produced by stretching the film in the machine direction by a factor of 5 and then stretching in the transverse direction by a tenter method at a stretching temperature of 110° C. and a stretching ratio of 2 times.

得られ九二軸延伸フィルムの引裂強度および透湿度の測
定結果を表1に示す。
Table 1 shows the results of measuring the tear strength and moisture permeability of the nine-biaxially stretched film obtained.

比較例3.4 実施例1における後段階の縦方向延伸温度を100℃(
比較例3)、12 QC(比較例4)とした外は、実施
例1と同様にして二輪延伸フィルムを製造した。
Comparative Example 3.4 The longitudinal stretching temperature in the later stage in Example 1 was changed to 100°C (
Comparative Example 3), 12 QC (Comparative Example 4) A two-wheel stretched film was produced in the same manner as in Example 1, except for using 12 QC (Comparative Example 4).

得られた二軸延伸フィルムの引裂強度および透湿度の測
定結果を表1に示す。
Table 1 shows the measurement results of the tear strength and moisture permeability of the obtained biaxially stretched film.

なお、各実施例、比較例とも、延伸フィルムの厚みが4
0μとなるように、押出機の吐出量を制御した。
In addition, in each example and comparative example, the thickness of the stretched film was 4
The discharge rate of the extruder was controlled so that it was 0μ.

表1 実施例3 実施例1におけるエチレン−ブテン−1共重合体に代え
て、プロピレン−エチレンブロック共重合体(エチレン
含有量3型看%、MFR9t/10分、轍点164℃)
を用い、押出温度を230℃とした外は、実施例1と同
様にしてフィルムを製造した。
Table 1 Example 3 In place of the ethylene-butene-1 copolymer in Example 1, a propylene-ethylene block copolymer (ethylene content 3%, MFR 9t/10 min, rut point 164°C)
A film was produced in the same manner as in Example 1, except that the extrusion temperature was 230°C.

このフィルムを、ロール延伸法により、延伸温度100
℃、延伸倍率4倍で縦方向に延伸し、次いで、テンター
法により、延伸温度160℃、延伸倍率8倍で横方向に
延伸した。その後、さらに、ロール延伸法により、延伸
温度80℃、延伸倍率1.4倍で縦方向に延伸すること
により、厚み40μの通気性フィルムを製造した。
This film was stretched at a stretching temperature of 100% by roll stretching method.
The film was stretched in the longitudinal direction at a stretching temperature of 160° C. and a stretching ratio of 4 times, and then stretched in the transverse direction by a tenter method at a stretching temperature of 160° C. and a stretching ratio of 8 times. Thereafter, the film was further stretched in the longitudinal direction by a roll stretching method at a stretching temperature of 80° C. and a stretching ratio of 1.4 times to produce a breathable film having a thickness of 40 μm.

得られた通気性フィルムの透湿度の測定結果を表2に示
す。
Table 2 shows the measurement results of the moisture permeability of the obtained breathable film.

実施例4 実施例3における後段階の縦方向延伸温度を120℃と
した外は、実施例3と同様にして通気性フィルムを製造
した。
Example 4 A breathable film was produced in the same manner as in Example 3, except that the longitudinal stretching temperature in the latter stage was 120°C.

得られた通気性フィルムの透湿度の測定結果を表2に示
す。
Table 2 shows the measurement results of the moisture permeability of the obtained breathable film.

比較例5.6 実施例3における後段階の縦方向延伸温度を140℃(
比較例5)、160℃(比較例6)とした外は、実施例
3と同様にして二軸延伸フィルムを製造した。
Comparative Example 5.6 The longitudinal stretching temperature in the later stage in Example 3 was changed to 140°C (
A biaxially stretched film was produced in the same manner as in Example 3, except that the temperature was 160° C. (Comparative Example 5) and 160° C. (Comparative Example 6).

得られ九二軸延伸フィルムの引裂強度の測定結果を表2
に示す。
Table 2 shows the measurement results of the tear strength of the obtained nine-biaxially stretched film.
Shown below.

表2 (ト)発明の効果 本発明の二軸延伸通気性フィルムの製造方法は、高度の
通気性を有する通気性フィルムが製造できるものである
Table 2 (G) Effects of the Invention The method for producing a biaxially stretched breathable film of the present invention can produce a breathable film having a high degree of air permeability.

特許出願人  三菱油化株式会社 代理人 弁理士 長 谷 正 久 (ほか1名)Patent applicant: Mitsubishi Yuka Co., Ltd. Agent: Patent Attorney Masahisa Nagatani (1 other person)

Claims (1)

【特許請求の範囲】[Claims] ポリオレフイン系樹脂42〜87体積%と無機充填剤5
8〜13体積%との組成物からなるフイルムを、同時ま
たは逐次に縦方向と横方向に二軸延伸した後、該ポリオ
レフイン系樹脂の融点より100℃から25℃低い範囲
の温度で、さらに縦方向に延伸することを特徴とする二
軸延伸通気性フイルムの製造方法。
Polyolefin resin 42-87% by volume and inorganic filler 5
After biaxially stretching a film consisting of a composition of 8 to 13% by volume in the longitudinal and transverse directions simultaneously or sequentially, it is further stretched longitudinally at a temperature in the range of 100°C to 25°C lower than the melting point of the polyolefin resin. 1. A method for producing a biaxially stretched breathable film, which comprises stretching in a direction.
JP18811086A 1986-08-11 1986-08-11 Production of biaxially oriented gas-permeable film Pending JPS6343932A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18811086A JPS6343932A (en) 1986-08-11 1986-08-11 Production of biaxially oriented gas-permeable film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18811086A JPS6343932A (en) 1986-08-11 1986-08-11 Production of biaxially oriented gas-permeable film

Publications (1)

Publication Number Publication Date
JPS6343932A true JPS6343932A (en) 1988-02-25

Family

ID=16217875

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18811086A Pending JPS6343932A (en) 1986-08-11 1986-08-11 Production of biaxially oriented gas-permeable film

Country Status (1)

Country Link
JP (1) JPS6343932A (en)

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