JPS63162734A - Production of porous film - Google Patents
Production of porous filmInfo
- Publication number
- JPS63162734A JPS63162734A JP30872086A JP30872086A JPS63162734A JP S63162734 A JPS63162734 A JP S63162734A JP 30872086 A JP30872086 A JP 30872086A JP 30872086 A JP30872086 A JP 30872086A JP S63162734 A JPS63162734 A JP S63162734A
- Authority
- JP
- Japan
- Prior art keywords
- film
- stretching
- stretched
- inorganic filler
- gas permeability
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000011256 inorganic filler Substances 0.000 claims abstract description 10
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 10
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 8
- 239000011342 resin composition Substances 0.000 claims abstract description 6
- 230000000704 physical effect Effects 0.000 abstract description 15
- 230000035699 permeability Effects 0.000 abstract description 11
- 230000000694 effects Effects 0.000 abstract description 3
- 239000010408 film Substances 0.000 abstract 7
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 239000010409 thin film Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 description 8
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 6
- 230000008018 melting Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000009423 ventilation Methods 0.000 description 4
- 230000009477 glass transition Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 238000005537 brownian motion Methods 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010227 cup method (microbiological evaluation) Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は充分な開口性を有し、透湿性、通気性が良好で
、物性バランスが非常に優れ、かつ引裂強度が優れたフ
ィルムに関するものである。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a film that has sufficient openness, good moisture permeability and air permeability, a very good balance of physical properties, and excellent tear strength. It is.
[従来の技術]
従来より、ポリオレフィン系樹脂に様々な非相溶性物質
を充填した樹脂組成物を製膜した後、延伸して、多孔性
フィルムが得られている(特公昭53−12542号、
特開昭56−99242号、特開昭57−59727号
、特開昭60−129240号等)。[Prior Art] Conventionally, a porous film has been obtained by forming a film from a resin composition in which a polyolefin resin is filled with various incompatible substances and then stretching the film (Japanese Patent Publication No. 53-12542,
JP-A-56-99242, JP-A-57-59727, JP-A-60-129240, etc.).
しかしながら、こわらの方法で得られたフィルムは縦方
向(フィルムの走行方向であり、以f&MDと称する)
と横方向(縦方向に垂直な方向、以1fiTDと称する
。)との物性、例えば引張強度などのバランスが悪く、
またMDに対しては引裂強度が弱いという欠点をもつ。However, the film obtained by Kowara's method is longitudinal (the running direction of the film, hereinafter referred to as f&MD).
and the lateral direction (direction perpendicular to the longitudinal direction, hereinafter referred to as 1fiTD), the physical properties such as tensile strength are poorly balanced
Moreover, it has the disadvantage that tear strength is weak compared to MD.
ポリオレフィン樹脂と、非相溶性物質として硫酸バリウ
ムを必須成分とするフィルムを少なくとも一軸方向に延
伸する特開昭60−129240号の方法においては非
常に改善されたものの、まだモ分なものでない。Although the method of JP-A-60-129240, in which a film containing a polyolefin resin and barium sulfate as an essential component as an incompatible substance is stretched in at least one direction, has been greatly improved, it is still not satisfactory.
一般にフィルムを延伸して上記MDとTDの物性バラン
スを向上させる方法として従来より縦延伸後横延伸を行
なう二軸延伸法が行なわれている(例えば特公昭30−
5639号)。In general, as a method for stretching a film to improve the physical property balance between MD and TD, a biaxial stretching method has traditionally been used in which longitudinal stretching is followed by transverse stretching (for example,
No. 5639).
無機充填物を用いる多孔性フィルムの場合には該二軸延
伸法を用いてもMDとTDとの物性バランス及び引裂強
度に優れたフィルムを得ることは不可能といえる。In the case of a porous film using an inorganic filler, it is impossible to obtain a film with excellent physical property balance between MD and TD and tear strength even if the biaxial stretching method is used.
すなわち、縦延伸を最初に行なう方法においては、縦延
伸倍率および縦延伸温度をどのように調整しようとも、
横延伸時に延伸安定性があり、かつ完成時に充分な通気
量をもちまた物性バランスおよび引裂強度にすぐれたフ
ィルムを成形することは不可能である。That is, in a method in which longitudinal stretching is performed first, no matter how the longitudinal stretching ratio and longitudinal stretching temperature are adjusted,
It is impossible to form a film that is stable during transverse stretching, has a sufficient amount of air permeability upon completion, and has an excellent balance of physical properties and tear strength.
これは、横延伸時にネッキングを起こさせる温度領域に
おいては、フィルムの裂けあるいはMD方向フィルム収
縮による破れが発生し成形が不可能となるからである。This is because, in a temperature range that causes necking during transverse stretching, film tearing or tearing due to film shrinkage in the MD direction occurs, making molding impossible.
一方、フィルムのネッキング延伸が起こらない温度領域
では成形は可能であるものの、横延伸後フィルムの延伸
部分は延伸開始点付近のみであり、延伸倍率を上げても
さらに延伸開始点付近が延伸され延伸部が横方向に伝播
してゆかないという欠点をもつため、充分な通気量を全
幅にわたって均一に得ることは不可能であり、物性バラ
ンス等も悪くなるからである。On the other hand, although forming is possible in a temperature range where necking stretching of the film does not occur, the stretched portion of the film after transverse stretching is only near the stretching start point, and even if the stretching ratio is increased, the stretching region near the stretching start point will be further stretched. This is because it has the disadvantage that the air flow does not propagate in the lateral direction, so it is impossible to obtain a sufficient amount of ventilation uniformly over the entire width, and the balance of physical properties becomes poor.
[発明が解決しようとする間π点]
本発明の目的は通気性を必要とする用途に応じて、MD
とTDの物性バランスおよび引裂強度に優れた多孔性フ
ィルムの製造法を提供することにある。[Pi point to be solved by the invention] The purpose of the present invention is to
An object of the present invention is to provide a method for producing a porous film having an excellent balance of physical properties between TD and TD and tear strength.
[問題点を解決するために手段]
本発明者らが上記目的を達成するため鋭意検討し、遂に
本発明を完成するに至った。[Means for Solving the Problems] The present inventors have made extensive studies to achieve the above object, and have finally completed the present invention.
即ち、本発明は、ポリオレフィン系樹脂100 l身部
と無機充填剤50〜500重量部から成る樹脂組成物を
溶融製膜してフィルムとし、しかる後、該フィルムを3
〜10倍に横延伸し、さらに1.1〜5倍に縦延伸する
ことを特徴とする多孔性フィルムの製造法である。That is, in the present invention, a resin composition consisting of 100 parts by weight of a polyolefin resin and 50 to 500 parts by weight of an inorganic filler is melt-formed into a film, and then the film is
This method of producing a porous film is characterized by horizontally stretching the film by a factor of 10 to 10, and then longitudinally stretching the film by a factor of 1.1 to 5.
以下、本発明の詳細な説明する。The present invention will be explained in detail below.
本発明におけるポリオレフィン、if−樹脂とは、ポリ
プロピレン、低密度ポリエチレン、線状低密度ポリエチ
レン、ホモブチレン等のホモ重合体、エチレン−プロピ
レン垂合体、エチレン−ブテン共重合体、エチレン−酢
酸ビニル共重合体等の共重合体あるいはこれらのブレン
ド物である。In the present invention, polyolefins and if-resins include polypropylene, low density polyethylene, linear low density polyethylene, homopolymers such as homobutylene, ethylene-propylene polymers, ethylene-butene copolymers, and ethylene-vinyl acetate copolymers. These are copolymers such as or blends thereof.
本発明における無機充填剤としては硫酸バリウム、炭酸
カルシウム、タルク、カオリン、塩化カルシウム、ケイ
素等の一種または二種以上を使用することができ、特に
硫酸バリウム、炭酸カルシウムが好ましく使用される。As the inorganic filler in the present invention, one or more of barium sulfate, calcium carbonate, talc, kaolin, calcium chloride, silicon, etc. can be used, and barium sulfate and calcium carbonate are particularly preferably used.
無機充填剤の使用量はポリオレフィン樹脂100ffi
ffi部当たり50〜500重量部であり、好ましくは
10(1〜400 fflffi部テアル。The amount of inorganic filler used is 100ffi of polyolefin resin.
50 to 500 parts by weight per part ffi, preferably 10 (1 to 400 parts ffffi).
この使用量が50重量部未満では通気量が十分得られず
、5(1(l fig部を超えて用いた場合にはフィル
ムの剛性が増し延伸がうまく行なえず、通気量が低下し
てしまう。If the amount used is less than 50 parts by weight, sufficient air permeability cannot be obtained, and if it is used in excess of 5 (1 (l) fig parts, the film becomes stiffer and cannot be stretched properly, resulting in a decrease in air permeability. .
次に本発明の多孔性フィルムの製造方法を説明する。Next, the method for producing the porous film of the present invention will be explained.
ポリオレフィン系樹脂および無機充填剤に、必要に応じ
て他の添加物を添加したのち、ヘンショルミキサー、ス
パーミキサー、タンブラ−型混合機を用いて混合し、そ
の後通常の一軸あるいは二軸スクリュー押出機によって
混練し、ベレット化する。次いで、これらのベレットを
インフレーション成形機あるいはTダイ成形機を用いて
製膜する。この際に、ベレット化せず、直接押し出し機
で製膜することもできる。After adding other additives to the polyolefin resin and inorganic filler as necessary, they are mixed using a Henshol mixer, a Spur mixer, or a tumbler type mixer, and then a conventional single or twin screw extruder. The mixture is kneaded and made into pellets. Next, these pellets are formed into a film using an inflation molding machine or a T-die molding machine. At this time, it is also possible to directly form a film using an extruder without pelletizing.
次に押出機により製膜したフィルムを、該フィルムのガ
ラス転移点以上、融点以下の間で、好ましくは40℃か
ら150℃、好ましくは60℃から120℃の間の温度
において3倍〜10倍に横方向へ延伸する。この場合、
温度が40℃未満の場合には伸度が降伏点を趙える以前
にフィルムに裂けが発生し延伸をうまく行なうことがで
きず、融点を越える場合には分子鎖の流動により、横延
伸時に満足のいく通気量を得ることができない。また、
延伸倍率が3倍未満の場合には一ト分な通気量が得られ
ない。あるいは延伸ムラが発生し縦延伸後も延伸ムラが
残るために商品価値を低落させる。また10倍を趙える
場合には延伸切れが発生し安定してフィルムを得ること
ができない。Next, the film formed by an extruder is heated 3 times to 10 times at a temperature between the glass transition point and melting point of the film, preferably between 40°C and 150°C, preferably between 60°C and 120°C. Stretch in the horizontal direction. in this case,
If the temperature is less than 40°C, the film will crack before the elongation reaches the yield point, making it difficult to stretch the film properly. If the temperature exceeds the melting point, the flow of molecular chains will cause the film to become unsatisfactory during transverse stretching. It is not possible to obtain adequate ventilation. Also,
If the stretching ratio is less than 3 times, a sufficient amount of ventilation cannot be obtained. Alternatively, stretching unevenness occurs and the stretching unevenness remains even after longitudinal stretching, reducing the commercial value. Further, if the stretching is increased by 10 times, stretching breakage occurs and a stable film cannot be obtained.
横延伸されたフィルムは次いで樹脂組成物のガラス転移
温度から融点の範囲内、好ましくは常温から融点(−2
0℃)の温度で縦方向に1.1〜5倍に延伸する。The transversely stretched film is then heated within the range of the glass transition temperature to the melting point of the resin composition, preferably from room temperature to the melting point (-2
The film is stretched 1.1 to 5 times in the machine direction at a temperature of 0°C.
1.1倍未満の場合は分子の配向効果が認められず、5
倍より大の場合は延伸切わの問題が発生する。If it is less than 1.1 times, no molecular orientation effect is observed, and 5
If it is larger than that, a problem of stretch cut will occur.
縦延伸の際に、温度が、樹脂組成物のガラス転移温度よ
り低い場合には、分子鎖のミクロブラウン運動の凍結に
より延伸は不可能である。また、融点より高い温度にお
いてはフィルムのロールへのべとつきが激しくなり延伸
が不可能である。During longitudinal stretching, if the temperature is lower than the glass transition temperature of the resin composition, stretching is impossible due to freezing of the micro-Brownian motion of the molecular chains. Furthermore, at temperatures higher than the melting point, the film becomes extremely sticky to the roll and cannot be stretched.
本発明のフィルムに示される引裂強度は、縦延伸後、横
延伸を行なう従来法によるフィルムでは得ることができ
ない。The tear strength exhibited by the film of the present invention cannot be obtained with films produced by conventional methods in which longitudinal stretching is followed by transverse stretching.
[実施例]
実施例1〜18 比較例1〜5
表1に示した樹脂と無機充填剤を表1に示した割合でヘ
ンシェルミキサーを用いて混合した後、二軸スクリュー
型混練機で均一に混練し、ベレットを作製した。これを
Tダイ押出し機を用いて溶融製膜した。その後、表1に
示す延伸条件でTDに延伸後、MDに延伸を行ない、表
1に示す物性のフィルムを得た。[Examples] Examples 1 to 18 Comparative Examples 1 to 5 The resins and inorganic fillers shown in Table 1 were mixed in the proportions shown in Table 1 using a Henschel mixer, and then uniformly mixed using a twin screw kneader. The mixture was kneaded to produce pellets. This was melted into a film using a T-die extruder. Thereafter, the film was stretched in the TD and then in the MD under the stretching conditions shown in Table 1 to obtain a film having the physical properties shown in Table 1.
比較例6〜11
実施例1と同様に製j漠したフィルムを1表1に示す延
伸条件で縦方向に延伸後、横方向に延伸し、表1に示す
物性のフィルムを得た。Comparative Examples 6 to 11 A film produced in the same manner as in Example 1 was stretched in the machine direction under the stretching conditions shown in Table 1, and then stretched in the transverse direction to obtain a film having the physical properties shown in Table 1.
比較例12
実施例1と同様に製膜したフィルムを、表1に示す延伸
条件で縦方向にのみ延伸し、表1に示す物性のフィルム
を得た。Comparative Example 12 A film produced in the same manner as in Example 1 was stretched only in the longitudinal direction under the stretching conditions shown in Table 1 to obtain a film with the physical properties shown in Table 1.
比較例!3
実施例1と同様に製膜したフィルムを、表1に示す延伸
条件で横方向にのみ延伸し、表1に示す物性のフィルム
を得た。Comparative example! 3 A film produced in the same manner as in Example 1 was stretched only in the transverse direction under the stretching conditions shown in Table 1 to obtain a film with the physical properties shown in Table 1.
尚、物性評価方法は以下の通りである。In addition, the physical property evaluation method is as follows.
(1)強度; 25[01!1 (幅) xloo+n
m (長さ)のフィルム片を弓1弓長りスピード20
0mm /minでテンション引張試験機にて測定する
。破談時強度をMD、TDについて各々測定する。(1) Strength; 25[01!1 (width) xloo+n
A piece of film of m (length) is bowed with a bow length speed of 20
Measurement is performed using a tension tensile tester at 0 mm /min. The intensity at the time of negotiation is measured for MD and TD respectively.
(2)透湿度、 ASTM E96−66(D)に準す
る。カップ法による32℃、 50%RH雰囲気下での
水分減少量
(3)伸度、JISに6732に準する。(2) Moisture permeability, according to ASTM E96-66(D). Moisture loss (3) Elongation measured by cup method at 32°C under 50% RH atmosphere, in accordance with JIS 6732.
試験片 25mm (巾) xloomm (長さ)
(4)引裂強度; JIS L 1085に準するが、
試験片の幅10a+m、長さ100mtn、切れ目50
mmとする。Test piece 25mm (width) xloomm (length)
(4) Tear strength: According to JIS L 1085,
Test piece width 10a+m, length 100mtn, cut 50
Let it be mm.
また、引張強度200mm/minとして引裂くときに
示す最低荷重と最大荷重の平均値をとる。Further, the average value of the minimum load and maximum load shown when tearing at a tensile strength of 200 mm/min is taken.
[発明の効果]
本発明の製造方法による多孔性フィルムは実施例からも
明らかの如く、非常にMDとTDとの物性バランスおよ
び引裂は強度に優れている。さらに本発明の製造方法は
、MDに延伸後、TDに延伸する方法よりも耳部の不良
幅が極端に少なくなり原料に対する収率が向上する。[Effects of the Invention] As is clear from the Examples, the porous film produced by the production method of the present invention has a very good physical property balance between MD and TD and excellent tear strength. Furthermore, in the manufacturing method of the present invention, the defective width of the edge portion is extremely smaller than in the method of stretching in the MD and then in the TD, and the yield based on the raw material is improved.
従来の多孔性フィルムは、一方向に裂けやすく、ざらに
一方向に伸び易く強度が小さいという欠点があったため
単体としては使用できず、また表面に露出する部分に使
用されたとしても補強剤を用いる必要があった。しかし
、本発明の製造方法による多孔性フィルムの場合は単体
としての用途はもちろんのこと、表面に露出する部分に
使用しても補強材の必要がなく、コスト的に存利となり
用途の拡大が可能となる。Conventional porous films have the disadvantages of being easily torn in one direction, easily stretching in one direction, and having low strength, so they cannot be used alone, and even if they are used in exposed areas, they require no reinforcing agents. It was necessary to use it. However, in the case of the porous film manufactured by the manufacturing method of the present invention, there is no need for reinforcing materials even if it is used not only as a single unit but also in the exposed part of the surface, which makes it cost-effective and expands the range of uses. It becomes possible.
例えば、従来使い捨てオムツなとでは着脱時の接着テー
プとは別に保護剥離テープを設ける必要があったが、本
発明によるフィルムを使用する場合には、TDの伸びが
小さく強度が大きいために保護剥離テープを必要としな
い。このことは非常にコストダウンにつながる。For example, with conventional disposable diapers, it was necessary to provide a protective release tape in addition to the adhesive tape when putting on and taking off diapers, but when using the film according to the present invention, the protective release tape can be removed because the TD elongation is small and the strength is high. Doesn't require tape. This leads to significant cost reduction.
また肌ざわりに優れているので、直接肌に接触する、防
水製をもたせたものに対して用いるのも存効であり、こ
の点からも用途の拡大が図れる。In addition, since it has an excellent texture, it is also effective to use it for waterproof items that come into direct contact with the skin, and from this point of view as well, the range of uses can be expanded.
本発明によるフィルムは以上の長所があるが、最大の特
徴は、その物性バランスを、延伸倍率を調整することに
よって用途に合わせて最も有用な乙のに設定することが
できる点にある。さらに通気量も使用目的に応じて自由
に選択することができる点も大きな特徴である。Although the film according to the present invention has the above-mentioned advantages, its greatest feature is that its physical property balance can be set to the most useful balance according to the application by adjusting the stretching ratio. Another major feature is that the amount of ventilation can be freely selected depending on the purpose of use.
Claims (1)
0〜500重量部から成る樹脂組成物を溶融製膜してフ
ィルムとし、しかる後、該フィルムを3〜10倍に横延
伸し、さらに1.1〜5倍に縦延伸することを特徴とす
る多孔性フィルムの製造法。1) 100 parts by weight of polyolefin resin and 5 parts by weight of inorganic filler
A resin composition comprising 0 to 500 parts by weight is melt-formed to form a film, and then the film is horizontally stretched 3 to 10 times, and further longitudinally stretched 1.1 to 5 times. Method of manufacturing porous film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30872086A JPH0684452B2 (en) | 1986-12-26 | 1986-12-26 | Method for producing porous film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30872086A JPH0684452B2 (en) | 1986-12-26 | 1986-12-26 | Method for producing porous film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63162734A true JPS63162734A (en) | 1988-07-06 |
JPH0684452B2 JPH0684452B2 (en) | 1994-10-26 |
Family
ID=17984469
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30872086A Expired - Lifetime JPH0684452B2 (en) | 1986-12-26 | 1986-12-26 | Method for producing porous film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0684452B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002264208A (en) * | 2001-03-15 | 2002-09-18 | Sumitomo Chem Co Ltd | Method for manufacturing porous film |
KR100885154B1 (en) | 2007-10-19 | 2009-02-25 | (주) 대동 | Method of breathable film having improved ventilation and tensile strength |
-
1986
- 1986-12-26 JP JP30872086A patent/JPH0684452B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002264208A (en) * | 2001-03-15 | 2002-09-18 | Sumitomo Chem Co Ltd | Method for manufacturing porous film |
KR100885154B1 (en) | 2007-10-19 | 2009-02-25 | (주) 대동 | Method of breathable film having improved ventilation and tensile strength |
Also Published As
Publication number | Publication date |
---|---|
JPH0684452B2 (en) | 1994-10-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4923650A (en) | Breathable microporous film and methods for making it | |
US5008296A (en) | Breathable microporous film | |
US5073316A (en) | Process for producing a porous film | |
JPS60129240A (en) | Porous film and its manufacture | |
US4829096A (en) | Breathable film and process for production of the same | |
JPS63276529A (en) | Air-permeable film manufactured from molten embossed polyolefine/filler precursor film | |
JPS62148537A (en) | Production of porous film | |
JPS62129321A (en) | Production of porous sheet | |
JPH08269220A (en) | Porous sheet and absorbing article made therefrom | |
JP3499652B2 (en) | Moisture permeable film | |
JPH10292059A (en) | Production of air-permeable film | |
JPH093226A (en) | Porous sheet and absorbing material using the same | |
JPS63162734A (en) | Production of porous film | |
JPH0550522A (en) | Manufacture of microscopically porous elastomer film | |
JPS6210141A (en) | Production of porous film or sheet | |
JPH02232238A (en) | Production of sheet | |
JP2001261868A (en) | Porous film and process for producing the same | |
JPS60199037A (en) | Porous film and manufacture thereof | |
JPH1135715A (en) | Production of porous film | |
JPH01204936A (en) | Resin composition for moisture-permeable film or sheet, moisture permeable film or sheet and preparation thereof | |
JP2002128928A (en) | Porous film and its manufacturing method | |
JPS62218428A (en) | Moisture-permeable film and its production | |
JPH0723432B2 (en) | Porous film | |
JPS63170431A (en) | Porous olefinic resin film | |
JP4054120B2 (en) | Porous film and method for producing the same |