JPS62201941A - Production of gas-permeable film or sheet - Google Patents
Production of gas-permeable film or sheetInfo
- Publication number
- JPS62201941A JPS62201941A JP4407086A JP4407086A JPS62201941A JP S62201941 A JPS62201941 A JP S62201941A JP 4407086 A JP4407086 A JP 4407086A JP 4407086 A JP4407086 A JP 4407086A JP S62201941 A JPS62201941 A JP S62201941A
- Authority
- JP
- Japan
- Prior art keywords
- sheet
- calcium carbonate
- powder
- particles
- film
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 42
- 239000002245 particle Substances 0.000 claims abstract description 37
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 14
- 238000002156 mixing Methods 0.000 claims abstract description 11
- 239000000843 powder Substances 0.000 claims abstract description 8
- 239000011362 coarse particle Substances 0.000 claims abstract description 7
- 239000010419 fine particle Substances 0.000 claims abstract description 7
- 238000003756 stirring Methods 0.000 claims abstract description 7
- 238000000354 decomposition reaction Methods 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 19
- -1 polyethylene Polymers 0.000 claims description 7
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 229920000092 linear low density polyethylene Polymers 0.000 claims description 6
- 239000004707 linear low-density polyethylene Substances 0.000 claims description 6
- 229920000573 polyethylene Polymers 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 2
- 229920013716 polyethylene resin Polymers 0.000 claims 1
- 230000035699 permeability Effects 0.000 abstract description 37
- 229920001577 copolymer Polymers 0.000 abstract description 3
- 230000001427 coherent effect Effects 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 230000003028 elevating effect Effects 0.000 abstract 1
- 239000000945 filler Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000009826 distribution Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000004299 exfoliation Methods 0.000 description 1
- 230000006355 external stress Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
Landscapes
- 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
Description
【発明の詳細な説明】
造方法に関する。詳しくは、樹脂に炭酸カルシウムの粒
子を充填剤として配合してなる組成物から、より改善さ
れた透気度、透湿度を有する透気性フィルム、またはシ
ートの製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a manufacturing method. Specifically, the present invention relates to a method for producing an air permeable film or sheet having improved air permeability and moisture permeability from a composition obtained by blending calcium carbonate particles as a filler into a resin.
従来の技術
従来より、ポリオレフィン樹脂て炭酸カルシウムを充填
剤として配合し、溶融成形して得られた原反フィルム、
またはシートを延伸し、透気性のよいフィルム、または
シートを製造する方法は広〈実施されている。Conventional technology Conventionally, raw films obtained by blending polyolefin resin with calcium carbonate as a filler and melt-molding,
Alternatively, a method of producing a film or sheet with good air permeability by stretching a sheet is widely practiced.
しかしながら、延伸後に得られた成形物の品質につい′
Cは、透気度、透湿度、機械的強度、柔軟性、風合い等
などの諸条件について要求される条件をすべて満足する
ものは得られていない。むしろすべての条件を満足する
というよりは、最終的需要目的に合せて、特性を強調す
べきであるとい5考え方が一般的である。たとえば使い
捨ておむつ等に利用されろ時は透気度、透湿度、および
風合いに特徴のあることが要求される。それらを満足す
るポリオレフィン樹脂としては線状低密度ポリエチレン
が好ましい(特開昭58− 149925、特開昭60
−185803参照)。However, the quality of the molded product obtained after stretching is
C has not been obtained that satisfies all the required conditions regarding air permeability, moisture permeability, mechanical strength, flexibility, texture, etc. Rather than satisfying all conditions, the general idea is that characteristics should be emphasized in accordance with the final demand objective. For example, when used in disposable diapers, it is required to have characteristics in air permeability, moisture permeability, and texture. Linear low-density polyethylene is preferable as a polyolefin resin that satisfies these requirements (Japanese Patent Laid-open No. 58-149925, Japanese Patent Laid-open No. 149925, No. 60)
-185803).
仮に,透気度、透湿度(C着目して改善を試みる場合、
製造工程中、充填剤を均一に配合する工程と、充填剤の
粒径が延伸工程で最も重要な要因になると考えられる。If we try to improve the air permeability and moisture permeability (C),
During the manufacturing process, the process of uniformly blending the filler and the particle size of the filler are considered to be the most important factors in the stretching process.
なお本願においてはインフレーション法、またはTダイ
法で得られるフィルム、/一トは原反フィルム、シート
と称し、これを延伸I−て得られるものを延伸(または
透気性)フィルム、シートと称l一て両者を区別するこ
ととする。In this application, the film obtained by the inflation method or the T-die method is referred to as a raw film or sheet, and the film obtained by stretching this is referred to as a stretched (or air permeable) film or sheet. Let us first distinguish between the two.
発明が解決し2よ5とする問題点
炭酸カルシウムを充填剤に選んだ場合、粒子同志の凝集
を防ぎ当該ポリエチレンとの均一分散性を実現しなけれ
ばならない。なぜなら、粒子の凝集は応力の集中を招き
、破壊核となってクラツクの成長を招くからである。Problems 2 and 5 solved by the invention When calcium carbonate is selected as a filler, it is necessary to prevent particles from agglomerating and to achieve uniform dispersibility with the polyethylene. This is because the agglomeration of particles causes concentration of stress, which becomes a fracture nucleus and causes the growth of cracks.
すでにいくつかの配合方法が提示されているが、本願発
明者は特公昭57 − 32941号の手法が原反フィ
ルム、シートを製造するに当って最,も優れていると考
え、その方式を採用した。なお、この先願で用いられて
いる樹脂は高密度ポリエチレンであるが、本願で扱う線
状低密度ポリエチレンと炭酸カルシウムの均一混合にも
利用できる。Although several compounding methods have already been proposed, the inventor of the present application believes that the method of Japanese Patent Publication No. 57-32941 is the most excellent for producing raw films and sheets, and adopted that method. did. Although the resin used in this prior application is high-density polyethylene, it can also be used for homogeneous mixing of linear low-density polyethylene and calcium carbonate, which are treated in the present application.
すなわち、一定の粒径からなる炭酸カルシウム粒子の所
定量から成る粉状混合物を攪拌下で、線状低密度ポリエ
チレン融点以上、分解点以下の温度に昇温させろことに
より凝集性粒状物を生成させた後、撹拌下で該ポリオレ
フィンの融点より低い温度まで冷却して得られる粒子組
成物を用いてインフレーション法、またはTダイ法とい
う通常の方法で原反フィルムまたはシートを作る。That is, a powder mixture consisting of a predetermined amount of calcium carbonate particles having a constant particle size is heated under stirring to a temperature above the melting point of linear low-density polyethylene and below the decomposition point, thereby producing cohesive granules. After that, the particle composition is cooled under stirring to a temperature lower than the melting point of the polyolefin, and a raw film or sheet is produced by a conventional method called an inflation method or a T-die method.
この工程において炭酸カルシウム粒子は徐々VC溶融す
るポリエチレン粒子表面に耐着し、これを包み、ついで
樹脂粒子内部からの溶融流動による樹脂の補給、炭酸カ
ルシウムの耐着という現象をくりかえし、両者の均一な
る混合が進むと考えられる。In this process, the calcium carbonate particles gradually adhere to the surface of the polyethylene particles melted by VC, wrap them, and then repeat the phenomenon of replenishing the resin by melting and flowing from inside the resin particles and adhering the calcium carbonate to the surface, so that both particles become uniform. It is thought that mixing will proceed.
さらに、ここで得られた原反フィルム、シー・トな用い
て透気性フィルム、シートを作るKは延伸方法が用いら
れこの延伸方法に瞥よロール加熱、熱板加熱、乾式オー
ブン加熱、湿式槽中での加熱媒体中で,一軸または二軸
方向に延伸すればよい。Furthermore, the raw film obtained here, sheet material is used to make air-permeable film, and the sheet is made by stretching methods. Stretching may be performed uniaxially or biaxially in a heating medium.
これにより透気性フィルムまたはシートが得られたが、
ざらに透気度、透湿度を改善するKは使用すべき炭酸カ
ルシウムの粒径、粒径分布、配合 等の複雑な相関を究
明する必要があることが明らかになった。This resulted in a permeable film or sheet, but
It has become clear that K, which roughly improves air permeability and moisture permeability, requires investigation of the complex relationship between the particle size, particle size distribution, and formulation of the calcium carbonate to be used.
問題点を解決するための手段 本発明は炭酸カルシウムの物性値と透気度。Means to solve problems The present invention focuses on the physical properties and air permeability of calcium carbonate.
透湿度の関係を追究する過程で見出されたものである。This was discovered in the process of investigating the relationship between moisture permeability.
通常、市販され、入手されろ炭酸カルシウムの粒子は1
〜6μmが最も多い。0.1μm 以下の粒子が多いと
粒子相互の凝集に伴う均一分散性が不良になるし、50
μm以上では外部応力によるフィラーマトリノクス界面
剥離によって発生し5たクレーズが大きくなりすぎごト
リックスが破壊されやすい。Usually, commercially available calcium carbonate particles are 1
~6 μm is the most common. If there are many particles of 0.1 μm or less, uniform dispersion becomes poor due to mutual agglomeration of particles, and
If it exceeds μm, the crazes generated due to exfoliation of the filler-matrix interface due to external stress will become too large and the matrix will be easily destroyed.
しかしながら、透気度、透湿度を対象とするとき、上記
炭酸カルシウムの粒径条件は更に厳格にならざるを得な
い。例えば延伸時に、1μm9下の粒子が多いと透気度
、透湿度が不充分となり6μmal上の粒子が多くなる
と、フィルム、シートは延伸切れを生ずるか風合いが著
しく損われるかの現象が見られ実用品に供し得ない。こ
うした背景から選ぶべき粒径は1〜6μmの範囲に限定
すべきであるとの結論を得た。However, when considering air permeability and water vapor permeability, the particle size conditions for calcium carbonate have to become even more stringent. For example, during stretching, if there are too many particles below 1 μm9, the air permeability and water vapor permeability will be insufficient, and if there are too many particles above 6 μm, the film or sheet will break in the stretch or the texture will be significantly impaired. It cannot be used as supplies. Based on this background, it was concluded that the particle size to be selected should be limited to a range of 1 to 6 μm.
配合量については、延伸を目的とするときはこの観点か
ら考慮されねばならない。炭酸カルシウムの配合量が該
線状低密度ポリエチレン100重竜部に対し80部未満
のときは延伸時に多孔質化が不充分で所望の透気度、透
湿度が得られない。また、200部を越えろときは粒子
の分散性、フィルムの加工性が劣り延伸性のみならず機
械的強度および風合いが不足し、実用性に乏しい。The amount to be blended must be considered from this point of view when the purpose is stretching. If the amount of calcium carbonate is less than 80 parts per 100 parts of the linear low-density polyethylene, porosity is insufficiently formed during stretching, and desired air permeability and moisture permeability cannot be obtained. On the other hand, if the amount exceeds 200 parts, the dispersibility of the particles and the processability of the film are poor, and not only the stretchability but also the mechanical strength and texture are insufficient, resulting in poor practicality.
本願発明者をよ以上のような過程で炭酸カルシウムの粒
径と添加遺を延伸の目的に合せて模索した。次に、この
範囲内で透気度、透湿度の優劣を比較検討したところ、
粒径分布がこれらの性能に著しい効果があることを見出
した。Through the process described above, the inventor of the present application searched for the particle size and addition of calcium carbonate in accordance with the purpose of stretching. Next, we compared and examined the superiority and inferiority of air permeability and moisture permeability within this range.
We have found that particle size distribution has a significant effect on these performances.
炭酸カルシウム粒子は種々の粒径のものが市販されてお
り、これらを混合することにより任意の分布をもった充
填剤を調整できる。なお、ここにいう代表的「平均粒径
」は空気透過式により測定した比表面積径を指す。Calcium carbonate particles with various particle sizes are commercially available, and by mixing these particles, a filler having an arbitrary distribution can be prepared. Note that the typical "average particle size" referred to herein refers to the specific surface area diameter measured by an air permeation method.
本願においては、二種の粒径の炭酸カルシウムを配合し
て性能を調べた。この結果、明らかに二つの極大を有す
る粒径分布を示す組成の配合が透気度、透湿度に好まI
−い結果を与えることが分った。In this application, performance was investigated by blending calcium carbonate with two different particle sizes. As a result, a composition with a particle size distribution that clearly has two maximums is preferable for air permeability and moisture permeability.
- It was found that it gave good results.
即ちここで次のように定義する。That is, it is defined here as follows.
(該ポリエチレン100重量部に対する重量部)この時
、R/r=1.5、かつM/m = 0 、1〜10の
ごとき配合が透気性、透過性の点で好ましい結果を示し
た。なおM+m−==80〜200部である。(Parts by weight relative to 100 parts by weight of the polyethylene) At this time, a blend of R/r = 1.5 and M/m = 0, 1 to 10 showed preferable results in terms of air permeability and permeability. Note that M+m-==80 to 200 parts.
即ち、粒径比R・/r<1.5の時は透気度、透湿度が
不充分であった。また、配合比M/m < 0.1、ま
たはM/m>10の時は良好な透気度、透湿度が達Fy
、されない。That is, when the particle size ratio R·/r<1.5, the air permeability and moisture permeability were insufficient. Also, when the blending ratio M/m < 0.1 or M/m > 10, good air permeability and moisture permeability are achieved.
, not done.
このようにR/r%M 7m の値がある範囲で透気度
、透湿度に著しい効果を与える理由は延伸工程で、粗粒
子と細粒子が適当に存在するとき最も効果的な空隙を形
成することに起因すると考えられる。しかも、この効果
は炭酸カルシウム粒子がポリエチレンに対して均一に分
散していることはもちろん粗粒子と細粒子の相互の分散
も均一であることによって可能と考えられろ。The reason why R/r%M 7m has a significant effect on air permeability and moisture permeability within a certain range is that the stretching process is most effective when coarse particles and fine particles exist appropriately. This is thought to be due to the fact that Moreover, this effect is thought to be possible not only because the calcium carbonate particles are uniformly dispersed in the polyethylene, but also because the mutual dispersion of coarse particles and fine particles is also uniform.
なお、線状低密度ポリエチレンには、エチレン−プロピ
レン共重合体、エチレン−酢酸ビニル共重合体、エチレ
ン−ブテン共重合体などの熱可塑性エラストマー及び高
密度ポリエチレン、低密度ポリエチレン(LDPE )
、ポリプロピレンを添加してもよい。これらは使用目的
に応じて成形物に充分な柔軟性を与えたり、機械的強度
を増したりかつ、風合いを改善したりするのに役Vつ。Note that linear low-density polyethylene includes thermoplastic elastomers such as ethylene-propylene copolymer, ethylene-vinyl acetate copolymer, and ethylene-butene copolymer, high-density polyethylene, and low-density polyethylene (LDPE).
, polypropylene may be added. These are useful in giving the molded product sufficient flexibility, increasing its mechanical strength, and improving its feel, depending on the purpose of use.
実施例
以下、本願の趣旨を実施例と比較例とを併記することに
より、より具体的に説明する。ここに示す実験は実験番
号1かも7までは次の条件に従った。但し、実験番号8
は注記による。EXAMPLES Hereinafter, the gist of the present application will be explained in more detail by writing together examples and comparative examples. The experiments shown here followed the following conditions up to experiment numbers 1 and 7. However, experiment number 8
According to the notes.
配合量は表示
ステアリン酸カルシウム 0.8重i1部これらをヘン
シェルミキサーで30分間混合し、150℃で凝集性粒
状組成物を生成せしめた後、撹拌下で70℃まで冷却し
、所定の粒状物を得ろ。そノ後50 m/m 96のイ
ンフレ押出機によりフイ/l/ ムヲ得た後、所定の延
伸倍率(表示)で延伸したく注:実験番号8は上記ヘン
シェルミキサーの操業をすべて常温で行った場合である
。その他の条件は記載どおり)。The blending amount is as follows: Calcium stearate 0.8 weight i 1 part These were mixed in a Henschel mixer for 30 minutes to form a cohesive granular composition at 150°C, and then cooled to 70°C with stirring to form a predetermined granular composition. Get it. Thereafter, after obtaining a film/l/mu with a 50 m/m 96 inflation extruder, it was stretched at a predetermined stretching ratio (displayed).Note: In experiment number 8, all operations of the above Henschel mixer were performed at room temperature. This is the case. Other conditions as stated).
インフレ押出条件
温度 シリンダルダイス 160〜190℃引取速度
Hm10 、折径350 m/m延伸条件
温度 70℃9倍率4.5倍及び3倍
速度
第1〜第3ロール速度 3・4〜31・60一ル10
m層 45夏n15+ 及び30m/分最
終フィルム厚み 20μm
フィルムの評価方法
透気度
JIS P8117法に準する
単位は秒/100m1で表わされ、数値の小さい程優れ
ており、大きい程劣ることを意味する。Inflation extrusion conditions temperature Cylinder die 160-190℃ Take-up speed
Hm10, folding diameter 350 m/m Stretching conditions temperature 70°C 9 magnification 4.5 times and 3 times speed 1st to 3rd roll speed 3.4 to 31.60 10
M layer 45 summer n15+ and 30m/min Final film thickness 20μm Film evaluation method Air permeability The unit according to JIS P8117 method is expressed in seconds/100m1, and the smaller the number, the better, and the larger the worse. do.
透湿度
JIS Z0208法に準する
単位は9/rri’ 24 Hourで表わされ、数値
の大きい程優れており、小さい程劣ることを意味する。The unit according to the moisture permeability JIS Z0208 method is expressed as 9/rri' 24 Hour, and the larger the value, the better, and the smaller the value, the worse.
発明の効果
本願の効果は、実施例と比較例の対比によって明らかで
ある。本願の条件によるときはいずれも延伸が良好で、
いずれも透気度、透湿度がすぐれ、目的とする透気性フ
ィルム、またはシートを製造できる。しかるに、本願の
条件によらない場合はほとんど延伸が不良か、風合いが
不良のため実用に供しえない。本願発明の透気性フィル
ムまたはシートは防水用衣料、濾過材料、医療用品、生
理用品および使い捨ておむつ等の分野に広く応用できる
。Effects of the Invention The effects of the present application are clear from a comparison between Examples and Comparative Examples. When the conditions of the present application are followed, the stretching is good in all cases.
Both have excellent air permeability and moisture permeability, and can be used to produce the desired air permeable film or sheet. However, if the conditions of the present application are not met, the stretching is poor or the texture is poor in most cases, making it impossible to put it to practical use. The air-permeable film or sheet of the present invention can be widely applied to fields such as waterproof clothing, filtration materials, medical supplies, sanitary products, and disposable diapers.
Claims (1)
てなる粉状混合物を攪拌下で、前記ポリエチレンの融点
以上、分解点以下の温度に昇温させることにより凝集性
粉状物を生成し、その後攪拌下で前記ポリエチレンの融
点より低い温度まで冷却して粉状組成物を形成し、この
組成物を押出成形により原反フィルム又はシートとし、
これをさらに延伸して透気性フィルムまたはシートを製
造する方法において、 前記炭酸カルシウムが細粒子部と粗粒子部の二つの粒子
部からなり、この場合粒子径の範囲はともに1〜6μm
の範囲内で、細粒子部と粗粒子部の平均粒子径の比は1
.5以上であり、前記ポリエチレン樹脂100重量部に
対して、前記細粒子部と粗粒子部を0.1〜10の重量
比で、かつ全体で80〜200性フィルム、またはシー
トの製造方法。[Claims] A cohesive powder is produced by heating a powder mixture prepared by blending calcium carbonate with a linear low-density polyethylene resin to a temperature above the melting point and below the decomposition point of the polyethylene while stirring. is then cooled under stirring to a temperature lower than the melting point of the polyethylene to form a powder composition, and this composition is extruded into a raw film or sheet,
In the method of producing an air-permeable film or sheet by further stretching the calcium carbonate, the calcium carbonate consists of two particle parts, a fine particle part and a coarse particle part, and in this case, the particle size range for both is 1 to 6 μm.
Within the range, the ratio of the average particle diameter of the fine particle part and the coarse particle part is 1
.. 5 or more, and the weight ratio of the fine particle part to the coarse particle part is 0.1 to 10 with respect to 100 parts by weight of the polyethylene resin, and the total weight ratio is 80 to 200.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4407086A JPS62201941A (en) | 1986-03-03 | 1986-03-03 | Production of gas-permeable film or sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4407086A JPS62201941A (en) | 1986-03-03 | 1986-03-03 | Production of gas-permeable film or sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62201941A true JPS62201941A (en) | 1987-09-05 |
Family
ID=12681367
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4407086A Pending JPS62201941A (en) | 1986-03-03 | 1986-03-03 | Production of gas-permeable film or sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62201941A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000198865A (en) * | 1999-01-04 | 2000-07-18 | Kao Corp | Production of porous film |
KR100338362B1 (en) * | 1999-07-23 | 2002-05-30 | 유승렬 | Composition for air permeabile film having excellent processability and permeability |
CN102205655A (en) * | 2011-04-19 | 2011-10-05 | 吴国逵 | Continuous production process of polyethylene (PE) breathable film |
CN103739962A (en) * | 2014-01-02 | 2014-04-23 | 上海紫华企业有限公司 | Polyolefin microporous air-permeable membrane and preparation method thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5732941A (en) * | 1980-08-06 | 1982-02-22 | Fujikura Ltd | Heat-shrinkable sheet |
JPS5815538A (en) * | 1981-07-22 | 1983-01-28 | Mitsubishi Chem Ind Ltd | Production of porous film or sheet |
JPS58149925A (en) * | 1982-03-02 | 1983-09-06 | Mitsubishi Chem Ind Ltd | Production of porous film or sheet |
JPS606439A (en) * | 1983-06-23 | 1985-01-14 | Mitsubishi Petrochem Co Ltd | Manufacture of gas-permeable film |
JPS60129240A (en) * | 1983-12-16 | 1985-07-10 | Mitsui Toatsu Chem Inc | Porous film and its manufacture |
JPS60185803A (en) * | 1984-03-05 | 1985-09-21 | 三井東圧化学株式会社 | Disposable diaper |
-
1986
- 1986-03-03 JP JP4407086A patent/JPS62201941A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5732941A (en) * | 1980-08-06 | 1982-02-22 | Fujikura Ltd | Heat-shrinkable sheet |
JPS5815538A (en) * | 1981-07-22 | 1983-01-28 | Mitsubishi Chem Ind Ltd | Production of porous film or sheet |
JPS58149925A (en) * | 1982-03-02 | 1983-09-06 | Mitsubishi Chem Ind Ltd | Production of porous film or sheet |
JPS606439A (en) * | 1983-06-23 | 1985-01-14 | Mitsubishi Petrochem Co Ltd | Manufacture of gas-permeable film |
JPS60129240A (en) * | 1983-12-16 | 1985-07-10 | Mitsui Toatsu Chem Inc | Porous film and its manufacture |
JPS60185803A (en) * | 1984-03-05 | 1985-09-21 | 三井東圧化学株式会社 | Disposable diaper |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000198865A (en) * | 1999-01-04 | 2000-07-18 | Kao Corp | Production of porous film |
KR100338362B1 (en) * | 1999-07-23 | 2002-05-30 | 유승렬 | Composition for air permeabile film having excellent processability and permeability |
CN102205655A (en) * | 2011-04-19 | 2011-10-05 | 吴国逵 | Continuous production process of polyethylene (PE) breathable film |
CN103739962A (en) * | 2014-01-02 | 2014-04-23 | 上海紫华企业有限公司 | Polyolefin microporous air-permeable membrane and preparation method thereof |
CN103739962B (en) * | 2014-01-02 | 2016-10-12 | 上海紫华企业有限公司 | Polyolefin micropore ventilated membrane and preparation method thereof |
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