JP2737236B2 - Method for producing breathable film - Google Patents

Method for producing breathable film

Info

Publication number
JP2737236B2
JP2737236B2 JP9973889A JP9973889A JP2737236B2 JP 2737236 B2 JP2737236 B2 JP 2737236B2 JP 9973889 A JP9973889 A JP 9973889A JP 9973889 A JP9973889 A JP 9973889A JP 2737236 B2 JP2737236 B2 JP 2737236B2
Authority
JP
Japan
Prior art keywords
nonwoven fabric
resin
breathable film
film
stretching
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.)
Expired - Fee Related
Application number
JP9973889A
Other languages
Japanese (ja)
Other versions
JPH02276636A (en
Inventor
清彦 中江
敏夫 川北
孝典 久米
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP9973889A priority Critical patent/JP2737236B2/en
Publication of JPH02276636A publication Critical patent/JPH02276636A/en
Application granted granted Critical
Publication of JP2737236B2 publication Critical patent/JP2737236B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B38/00Ancillary operations in connection with laminating processes
    • B32B38/0032Ancillary operations in connection with laminating processes increasing porosity

Landscapes

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

Description

【発明の詳細な説明】 <産業上の利用分野> 本発明は通気性フィルムの製造方法に関する。さらに
詳しくは、空気、水蒸気を透過させるが水は不透過であ
る通気性フィルムの製造方法において、高い強度と高い
耐水圧を持った通気性フィルムを供給するための通気性
フィルムの製造方法に関する。
The present invention relates to a method for producing a breathable film. More specifically, the present invention relates to a method for producing a breathable film that allows air and water vapor to pass therethrough but does not allow water to pass through, and relates to a method for producing a breathable film for supplying a breathable film having high strength and high water pressure resistance.

<従来の技術> 従来、水不透過であり通気、水蒸気等の基体を透過す
る通気性フィルムは、紙おむつのバックシート、吸湿剤
や脱酸素剤の包装などに用いられている。その製造方法
としては特開昭60−229731号公報に記載のように樹脂と
充填剤とからなる組成物や、場合によってはさらに、こ
れにワックス状の炭化水素重合体を加えてなる組成物を
フィルム化し、延伸せしめることによりフィルム内部に
ミクロボイドを発生させて通気性を発現させるものがあ
る。しかし、樹脂と充填剤とからなるフィルムは引張強
度、引裂強度共に限界があった。また、小さい応力に対
する伸びが大きくなるために耐水圧が低くなるという問
題や物理的に充填剤と樹脂の間にミクロボイドを発生さ
せるためにミクロボイドの大きい部分と小さい部分が発
生し、通気度や強度の均一性を妨げるという問題があっ
た。
<Conventional Technology> Conventionally, a breathable film that is impermeable to water and that is permeable to a substrate such as aeration and water vapor has been used for a back sheet of a disposable diaper, packaging of a moisture absorbent and a deoxidizer, and the like. As a method for producing the composition, a composition comprising a resin and a filler as described in JP-A-60-229731 or, in some cases, a composition obtained by adding a waxy hydrocarbon polymer to the composition. In some cases, a film is formed and stretched to generate microvoids inside the film to exhibit air permeability. However, a film comprising a resin and a filler has limitations in both tensile strength and tear strength. In addition, there is a problem that the water pressure resistance is reduced due to the increase in elongation for small stress, and large and small portions of microvoids are generated due to physical generation of microvoids between the filler and the resin. There is a problem that hinders uniformity.

これらの課題を解決するための方法としては不織布な
どの補強材を通気性フィルムに配する方法がある。例え
ば、特開昭63−286330号公報のように通気性フィルムに
不織布を部分貼合したり、特開昭63−116849号公報や実
開昭63−136926号公報のように、接着層を選定し通気性
フィルムと不織布を全面貼合する手法はすでに公知であ
る。
As a method for solving these problems, there is a method of arranging a reinforcing material such as a nonwoven fabric on a breathable film. For example, as described in JP-A-63-286330, a nonwoven fabric is partially bonded to a breathable film, or an adhesive layer is selected as in JP-A-63-116849 or JP-A-63-136926. The technique of laminating the breathable film and the nonwoven fabric on the entire surface is already known.

ところが、通気性フィルムと不織布を部分貼合する場
合、貼合部と未貼合部に通気性の差が生じたり、未貼合
部に応力集中が起こるために耐水圧が低くなったりして
好ましくなく、また、接着層を選定し通気性フィルムと
不織布を全面貼合する方法は、接着層の厚みを薄く均一
にコントロールしなければ通気度が変化したり接着強度
が均一にならないという問題点があった。
However, when the air-permeable film and the nonwoven fabric are partially bonded, a difference in air permeability may occur between the bonded portion and the non-bonded portion, or the water pressure may be reduced due to stress concentration in the non-bonded portion. Also, the method of selecting an adhesive layer and laminating the air permeable film and the nonwoven fabric over the entire surface is problematic in that the air permeability changes or the adhesive strength is not uniform unless the thickness of the adhesive layer is controlled to be thin and uniform. was there.

<課題を解決するための手段> 本発明者らは、均質な高い通気度と高い強度を持つ通
気性フィルムを得る方法について鋭意研究を続けてき
た。その結果、樹脂と充填剤からなる樹脂組成物を特定
の不織布上にラミネートした後、該不織布と同時に延伸
することにより均質な高い通気度と高い強度を持つ通気
性フィルムとなることを見いだし本発明に至った。
<Means for Solving the Problems> The present inventors have intensively studied a method for obtaining a uniform breathable film having high air permeability and high strength. As a result, after laminating a resin composition comprising a resin and a filler on a specific non-woven fabric, and stretching the resin at the same time as the non-woven fabric, it was found that a uniform breathable film having high air permeability and high strength was obtained. Reached.

すなわち本発明は、 熱可塑性樹脂100重量部と充填剤50〜400重量部からな
る樹脂組成物を厚さ10μm〜400μmの不織布上に溶融
ラミネートした後、該不織布と同時に一軸または二軸に
1.1〜3.0倍の倍率で延伸する方法において、該不織布が
40℃より高く、樹脂組成物の溶融ラミネート温度より50
℃以上低い融点を持つ樹脂組成物を含むものであること
を特徴とする通気性フィルムの製造方法である。
That is, the present invention, after melt-laminating a resin composition comprising 100 parts by weight of a thermoplastic resin and 50 to 400 parts by weight of a filler on a nonwoven fabric having a thickness of 10 μm to 400 μm, uniaxially or biaxially simultaneously with the nonwoven fabric.
In the method of stretching at a magnification of 1.1 to 3.0 times, the nonwoven fabric is
Higher than 40 ° C and higher than the melt lamination temperature of the resin composition
A method for producing a breathable film, comprising a resin composition having a melting point lower by at least ° C.

通気性フィルム用の熱可塑性樹脂としては、例えば、
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、ポリブテン等のα−オレフィンホモポリマー、エ
チレンと炭素数3〜18の少なくとも一種のα−オレフィ
ンとの共重合体、プロピレンとエチレンおよび/または
ブテン−1との共重合体、エチレンと酢酸ビニルおよび
/またはアクリル酸エステル・メタアクリル酸エステル
類などエチレン性不飽和結合を有する有機カルボン酸誘
導体との共重合体などが挙げられる。
As a thermoplastic resin for a breathable film, for example,
Α-olefin homopolymers such as low-density polyethylene, high-density polyethylene, polypropylene, and polybutene, copolymers of ethylene and at least one α-olefin having 3 to 18 carbon atoms, propylene and ethylene and / or butene-1 Copolymers, and copolymers of ethylene with an organic carboxylic acid derivative having an ethylenically unsaturated bond such as vinyl acetate and / or acrylates / methacrylates, and the like can be given.

特にエチレンと炭素数3〜8の少なくとも一種のα−
オレフィンとの共重合体が充填剤配合時の強度の点から
好ましく、さらに低密度ポリエチレンとエチレンと炭素
数3〜8の少なくとも一種のα−オレフィンとの共重合
体のブレンドがフィルムの加工性、延伸性の点から好ま
しくない。また、本発明においては1.1〜3.0倍の低倍率
延伸で高い通気性を発現するために、熱可塑性樹脂は、
密度0.920g/cm3以上である樹脂を40重量%以上含むこと
が好ましい。
In particular, ethylene and at least one kind of α-
Copolymers with olefins are preferred from the viewpoint of the strength at the time of compounding the filler, and blends of low-density polyethylene, a copolymer of ethylene and at least one α-olefin having 3 to 8 carbon atoms form a film having processability, It is not preferable from the viewpoint of stretchability. Further, in the present invention, in order to express high air permeability at a low draw ratio of 1.1 to 3.0 times, the thermoplastic resin,
It is preferable to contain 40% by weight or more of a resin having a density of 0.920 g / cm 3 or more.

本発明において、熱可塑性樹脂100重量部に対する充
填剤の量が50重量部未満の場合は、延伸後に通気性を発
現することが難しく、また、400重量部を超える場合
は、加工性が悪化するために好ましくない。特に、加工
安定性の面から、充填剤は70〜200重量部が好ましい。
In the present invention, if the amount of the filler is less than 50 parts by weight based on 100 parts by weight of the thermoplastic resin, it is difficult to develop air permeability after stretching, and if it exceeds 400 parts by weight, processability is deteriorated. Not preferred. Particularly, from the viewpoint of processing stability, the amount of the filler is preferably 70 to 200 parts by weight.

充填剤の例として、炭酸カルシウム、炭酸マグネシウ
ム、炭酸バリウムなどの炭酸塩、硫酸バリウム、硫酸マ
グネシウム、硫酸カルシウムなどの硫酸塩、リン酸マグ
ネシウム、リン酸カルシウムなどのリン酸塩、水酸化マ
グネシウム、水酸化アルミニウムなどの水酸化物、アル
ミナ、シリカ、酸化マグネシウム、酸化カルシウム、酸
化亜鉛、酸化チタンなどの酸化物、塩化亜鉛、塩化鉄、
塩化ナトリウムなどの塩化物、アルミニウム粉、ゼオラ
イト、シラス、白土、珪藻土、タルク、カーボンブラッ
ク、火山灰などの無機充填剤や木粉、パルプ粉などのセ
ルロース系粉末、ナイロン粉末、ポリカーボネート粉
末、ポリプロピレン粉末、ポリ−4−メチルベンテン−
1粉末などの合成樹脂系粉末、でん粉などの有機充填剤
を挙げることができ、これらは単独または組み合わせて
使用される。フィルムの通気性、柔軟性・外観などの点
から炭酸カルシウムが特に好ましい。充填剤の平均粒径
は0.1〜20μmの充填剤の分散によるフィルムの均一性
の点から好ましく、特に0.8〜5.0μmのものが加工性の
点から好ましい。
Examples of the filler include carbonates such as calcium carbonate, magnesium carbonate and barium carbonate, sulfates such as barium sulfate, magnesium sulfate and calcium sulfate, phosphates such as magnesium phosphate and calcium phosphate, magnesium hydroxide, and aluminum hydroxide. Hydroxides, oxides such as alumina, silica, magnesium oxide, calcium oxide, zinc oxide, titanium oxide, zinc chloride, iron chloride, etc.
Chlorides such as sodium chloride, aluminum powder, zeolite, shirasu, clay, diatomaceous earth, talc, carbon black, inorganic fillers such as volcanic ash, wood powder, cellulose powder such as pulp powder, nylon powder, polycarbonate powder, polypropylene powder, Poly-4-methylbenthene-
Organic powders such as synthetic resin-based powders such as No. 1 powder and starch, and these can be used alone or in combination. Calcium carbonate is particularly preferred from the viewpoint of air permeability, flexibility and appearance of the film. The average particle size of the filler is preferably from the viewpoint of uniformity of the film due to dispersion of the filler of 0.1 to 20 μm, and particularly preferably from 0.8 to 5.0 μm from the viewpoint of processability.

本発明は延伸により通気性を発現する樹脂組成物を通
気性のある不織布上にラミネートした後不織布と同時に
延伸するものであるから、不織布の厚みは10〜400μm
が好ましい。10μm未満の場合は延伸後の強度が期待で
きない。また、400μmを超える場合は、延伸性が悪く
なり好ましくない。
Since the present invention is to stretch simultaneously with the nonwoven fabric after laminating the resin composition that expresses air permeability by stretching on the nonwoven fabric, the thickness of the nonwoven fabric is 10 to 400 μm
Is preferred. If it is less than 10 μm, the strength after stretching cannot be expected. On the other hand, if it exceeds 400 μm, the stretchability becomes poor, which is not preferable.

本発明においては不織布上に溶融ラミネートした後不
織布と同時に延伸するために該樹脂組成物と不織布との
密着強度が高くないと延伸時に剥離してしまうため、不
織布としては40℃より高く該樹脂組成物の溶融ラミネー
ト温度よりも50℃以上低い融点を持つ低融点樹脂成分を
少なくとも1種類以上含むものを使用する。このような
不織布としては、例えば、単独樹脂成分からなる不織布
に該低融点樹脂成分を溶液浸漬により付着させたもの
や、2種類以上の樹脂成分をそれぞれ繊維にして混成し
てなるもの、繊維を2種類以上の樹脂成分で混成し、不
織布としたものなどが挙げられる。繊維を2種類以上の
樹脂成分で混成したものとしては、例えば、芯層と鞘層
からなる同心多層タイプや、各々の樹脂が偏心した多層
タイプで鞘層の一部または全部が該低融点樹脂であるも
の、繊維の一部が少なくとも該低融点樹脂であってそれ
が繊維表面に連続的または断続的にあらわれているもの
などが挙げられる。特に、不織布の強度の点からは、芯
層と鞘層を持つ繊維より成り、少なくとも最外層の鞘層
が低融点樹脂成分からなる不織布が好ましい。溶融ラミ
ネート温度と不織布の一部または全部を構成する樹脂成
分の融点の差が50℃未満の場合は溶融ラミネート時に密
着強度がでないために好ましくなく、樹脂成分の融点が
40℃未満の場合、特に夏場のフィルム加工時に、フィル
ムの粘着性が非常に増大し、ロール離れが悪くなり、ト
ラブルの原因となるため好ましくない。
In the present invention, since the resin composition and the non-woven fabric are stretched simultaneously with the non-woven fabric after being melt-laminated on the non-woven fabric, if the adhesive strength between the resin composition and the non-woven fabric is not high, the resin composition will peel off during stretching. A material containing at least one or more low-melting resin components having a melting point lower by at least 50 ° C. than the melt lamination temperature of the product is used. As such a nonwoven fabric, for example, a nonwoven fabric composed of a single resin component, the low-melting-point resin component adhered by solution immersion, or a mixture obtained by mixing two or more resin components into fibers, fibers, Nonwoven fabrics formed by mixing two or more resin components are exemplified. Examples of a fiber obtained by mixing fibers with two or more resin components include a concentric multilayer type including a core layer and a sheath layer, and a multilayer type in which each resin is eccentric and a part or all of the sheath layer is formed of the low melting point resin. And a fiber in which at least a part of the fiber is at least the low-melting resin, which is continuously or intermittently appeared on the fiber surface. In particular, from the viewpoint of the strength of the nonwoven fabric, a nonwoven fabric made of a fiber having a core layer and a sheath layer, and at least the outermost sheath layer made of a low-melting resin component is preferable. If the difference between the melt lamination temperature and the melting point of the resin component constituting part or all of the nonwoven fabric is less than 50 ° C., it is not preferable because the adhesive strength is not at the time of melt lamination, and the melting point of the resin component is low.
If the temperature is lower than 40 ° C., particularly during film processing in summer, the tackiness of the film is extremely increased, the roll separation becomes poor, and it is not preferable because it causes trouble.

不織布の一部または全部を構成する樹脂成分としては
例えば、ポリエステル、ナイロンや、ポリエチレン、ポ
リプロピレン、ポリブテン等のα−オレフィンホモポリ
マー、エチレンと炭素数3〜18の少なくとも1種のα−
オレフィンとの共重合体、プロピレンとエチレンおよび
/またはブテン−1との共重合体、エチレンと酢酸ビニ
ルおよび/またはアクリル酸エステル・メタアクリル酸
エステル類などエチレン性不飽和結合を有する有機カル
ボン酸誘導体との共重合体などが挙げられる。
Examples of the resin component constituting part or all of the nonwoven fabric include polyester, nylon, and α-olefin homopolymers such as polyethylene, polypropylene, and polybutene; ethylene and at least one α-olefin having 3 to 18 carbon atoms.
Organic carboxylic acid derivatives having an ethylenically unsaturated bond such as copolymers with olefins, copolymers with propylene and ethylene and / or butene-1, ethylene and vinyl acetate and / or acrylates and methacrylates And the like.

特に、加工性や強度、密着性などから芯層がポリエス
テルであり鞘層がポリエチレンであることが好ましく、
例えば、ユニチカ(株)製のエルベス、大和紡績(株)
製のNBF、クラレ(株)製のソフィト等が挙げられる。
In particular, the core layer is preferably polyester and the sheath layer is preferably polyethylene from the viewpoint of workability, strength, and adhesion,
For example, Elbes manufactured by Unitika Ltd., Daiwa Spinning Co., Ltd.
NBF manufactured by Kuraray Co., Ltd., and the like.

本発明における通気性フィルムは熱可塑性樹脂と充填
剤、必要に応じては分散剤や安定剤などを、ロール型ま
たはバンバリー型の混練機あるいは一軸または二軸押出
機などを用いる通常の方法で混合あるいは混練して組成
物を得る。次いでこの組成物を不織布の上に5〜150μ
mの範囲でラミネート加工したものを延伸することによ
り通気製を発現させるものであるが、延伸は一軸また二
軸で行なわれる。一軸延伸の場合は通常ロール延伸が好
ましい。二軸延伸の場合は同時二軸延伸でも可能である
し、縦方向の延伸を行なった後に横方向を延伸する逐次
二軸延伸でも可能である。適切な延伸倍率は樹脂成分や
不織布の種類により異なるが、1.1〜3.0倍の延伸倍率が
好ましい。1.1倍未満の場合は通気性が期待できず、3.0
倍を超えると素材の破断などの影響が出たり、縦方向の
引裂強度が低下するため好ましくない。より好ましい延
伸倍率は、1.2〜2.0倍である。延伸温度は樹脂組成によ
って異なるが通常は30〜140℃の範囲が好ましい。30℃
未満の場合は延伸時の安定性が好ましくなく、140℃を
超える場合はミクロボイドが発生しにくいため好ましく
ない。特に、30〜140℃の範囲で延伸を行なった後に、8
0℃〜170℃の範囲で熱セットすることがフィルムのシワ
を防止する点で好ましい。
In the present invention, the breathable film is prepared by mixing a thermoplastic resin and a filler, and if necessary, a dispersant and a stabilizer by a usual method using a roll-type or Banbury-type kneader or a single- or twin-screw extruder. Alternatively, the composition is obtained by kneading. This composition is then placed on a nonwoven fabric for 5-150μ.
The laminated product is stretched in the range of m so as to exhibit air permeability, but the stretching is performed uniaxially or biaxially. In the case of uniaxial stretching, roll stretching is usually preferred. In the case of biaxial stretching, simultaneous biaxial stretching is also possible, or sequential biaxial stretching in which stretching in the longitudinal direction is performed and then stretching in the transverse direction is also possible. The appropriate stretching ratio varies depending on the type of the resin component and the nonwoven fabric, but a stretching ratio of 1.1 to 3.0 times is preferable. If it is less than 1.1 times, breathability cannot be expected, and 3.0
Exceeding the number of times is undesirable because the material may be broken or the tear strength in the longitudinal direction may be reduced. A more preferred stretching ratio is 1.2 to 2.0 times. The stretching temperature varies depending on the resin composition, but is usually preferably in the range of 30 to 140 ° C. 30 ℃
If it is less than 1, the stability at the time of stretching is not preferable, and if it exceeds 140 ° C., microvoids are not easily generated, which is not preferable. In particular, after stretching in the range of 30 to 140 ° C, 8
Heat setting in the range of 0 ° C. to 170 ° C. is preferable from the viewpoint of preventing film wrinkles.

<作用> 本発明において不織布に熱可塑性樹脂100重量部と充
填剤50〜400重量部かなる樹脂組成物を溶融ラミネート
した後に延伸するのは、不織布と多孔質フィルムとの密
着面を広げることと、延伸時に均一なミクロボイドを形
成させることによって通気度と強度を均一にすることが
目的である。
<Function> In the present invention, stretching after melt-laminating a resin composition comprising 100 parts by weight of a thermoplastic resin and 50 to 400 parts by weight of a filler to a nonwoven fabric involves expanding the adhesion surface between the nonwoven fabric and the porous film. The purpose is to make uniform air permeability and strength by forming uniform microvoids during stretching.

本発明は、特定の不織布に樹脂組成物を溶融ラミネー
トした後に延伸することによって延伸開始点が幅広く分
散し、これによって通気性フィルムの均一な開孔性すな
わち、均一な通気度と均一な強度が発現されるものであ
る。
In the present invention, a stretching start point is widely dispersed by stretching after melt-laminating the resin composition on a specific nonwoven fabric, whereby uniform porosity of a breathable film, that is, uniform air permeability and uniform strength are obtained. Is to be expressed.

また、延伸後の接着や融着などの処理がないために通
気性や強度を損なうことがない。
Further, since there is no treatment such as adhesion or fusion after stretching, air permeability and strength are not impaired.

<発明の効果> 本発明の通気性フィルムの製造方法によって得られた
通気性フィルムは強度および通気性に優れ、かつ、フィ
ルムのどの部分をとっても、それら物性が均一で安定し
ている。吸湿剤、酸素吸収剤などの包装材料などの均質
な通気性が必要である用途や、壁紙、洋服カバーなどの
高い強度と透湿性が必要である用途に極めて有用であ
る。
<Effect of the Invention> The breathable film obtained by the method for producing a breathable film of the present invention has excellent strength and breathability, and the physical properties thereof are uniform and stable regardless of the portion of the film. It is extremely useful for applications that require uniform air permeability, such as packaging materials such as moisture absorbers and oxygen absorbers, and applications that require high strength and moisture permeability, such as wallpaper and clothes covers.

<実施例> 以下、実施例によって詳細に説明するが、本発明はこ
れによって限定されるものではない。実施例および比較
例に示した透湿度および耐水圧、強度、延伸ムラ、不織
布と樹脂組成物との密着性は以下の基準で判定した。
<Example> Hereinafter, an example will be described in detail, but the present invention is not limited thereto. The moisture permeability, water pressure resistance, strength, stretching unevenness, and adhesion between the nonwoven fabric and the resin composition shown in Examples and Comparative Examples were determined according to the following criteria.

通気度:JIS Z0208準拠、40℃、90%RHの条件で水蒸気
の透過度を測定した。
Air permeability: Water vapor permeability was measured under the conditions of 40 ° C. and 90% RH in accordance with JIS Z0208.

耐水圧:JIS L1092−A法により試験片の裏側に3ケ所
から水が出たときの水位を測定した。
Water pressure: The water level when water came out from three places on the back side of the test piece was measured by the JIS L1092-A method.

延伸ムラ:延伸ムラの状態を目視にて判定し、以下の基
準で×〜○を決定した。
Stretch unevenness: The state of stretch unevenness was visually determined, and x to ○ were determined based on the following criteria.

○:延伸ムラは全く見られず均一に延伸されている。:: Uniform stretching was observed without any stretching unevenness.

△:一部に延伸ムラが見られるが未延伸部との間隔は5m
m以内が殆どである。
Δ: Stretch unevenness is observed in part, but the distance from the unstretched part is 5 m
Most are within m.

×:延伸ムラがはっきり見られ5mmを超える未延伸部分
が多数存在する。
×: Stretching unevenness is clearly seen, and there are many unstretched portions exceeding 5 mm.

密着性:不織布と熱可塑性樹脂組成物からなるフィルム
との延伸後の密着の状態を目視および樹脂にて判定し、
以下の基準で×〜○を決定した。
Adhesion: The state of adhesion between the nonwoven fabric and the film made of the thermoplastic resin composition after stretching is determined visually and by resin,
× to ○ were determined based on the following criteria.

○:不織布とフィルムとの剥離は全く見られず均一に密
着している。
:: No separation between the nonwoven fabric and the film was seen at all, and the film was uniformly adhered.

△:不織布とフィルムに部分的に剥離している部分があ
り、手で不織布からフィルムを剥がすことができる。
Δ: The nonwoven fabric and the film have partially peeled portions, and the film can be peeled from the nonwoven fabric by hand.

×:不織布とフィルムが殆ど剥離している。X: The nonwoven fabric and the film are almost peeled off.

実施例1 線状低密度ポリエチレン(住友化学工業(株)製スミ
カセン α CS3003、密度0.932g/cm3)75重量%と高圧
法低密度ポリエチレン(住友化学工業(株)製スミカセ
ン F208−0、密度0.922g/cm3)25重量%とからなる熱
可塑性樹脂100重量部と炭酸カルシウム(白石カルシウ
ム(株)製ホワイトンSSB(赤))150重量部とからなる
組成物をバンバリー型の混練機で混練した後、芯層がポ
リエステル(融点257℃)、鞘層がポリエチレン(融点1
24℃)である同心の繊維からなる厚さ100μm、坪量30g
/m2の不織布(ユニチカ(製)エルベスS0303WD0)に270
℃の樹脂温度にて、30g/m2の坪量でラミネートした。こ
のラミネートフィルムをロール型の延伸機で一軸方向に
50℃で1.3倍延伸することにより通気性フィルムを得
た。得られた通気性フィルムは、表1に示すように高い
通気性と耐水圧および温度、均一延伸性(ムラの無い)
および良好な密着性を示した。
Example 1 75% by weight of linear low-density polyethylene (Sumikasen α CS3003 manufactured by Sumitomo Chemical Co., Ltd., density: 0.932 g / cm 3 ) and high-pressure low-density polyethylene (Sumikasen F208-0 manufactured by Sumitomo Chemical Co., Ltd., density: 0.922 g / cm 3 ) A composition consisting of 100 parts by weight of a thermoplastic resin consisting of 25% by weight and 150 parts by weight of calcium carbonate (whiten SSB (red) manufactured by Shiraishi Calcium Co., Ltd.) was mixed with a Banbury-type kneader. After kneading, the core layer is made of polyester (melting point 257 ° C), and the sheath layer is made of polyethylene (melting point 1).
24 ° C) Concentric fiber thickness 100μm, basis weight 30g
/ m 2 non-woven fabric (Unitika (product) Elves S0303WD0) 270
Lamination was performed at a resin temperature of 30 ° C. and a basis weight of 30 g / m 2 . This laminate film is uniaxially stretched by a roll-type stretching machine.
The film was stretched 1.3 times at 50 ° C. to obtain a breathable film. As shown in Table 1, the obtained air-permeable film has high air permeability, water resistance, temperature, and uniform stretchability (without unevenness).
And good adhesion.

実施例2 不織布として、芯層がポリプロピレン(融点165
℃)、鞘層がポリエチレン(融点130℃)の偏心タイプ
の繊維(チッソ(株)製ES繊維、芯層は一部表面に露出
している)からなる厚さ150μm、坪量20g/m2のもの
(不織布は通常の乾式法により作製した)を使用した以
外は実施例1と同様にして通気性フィルムを得た。得ら
れた通気性フィルムは実施例1と同様の良好な物性を示
した。
Example 2 As a nonwoven fabric, the core layer was made of polypropylene (melting point 165).
° C), and the sheath layer is made of polyethylene (melting point: 130 ° C) eccentric type fiber (ES fiber manufactured by Chisso Corp., the core layer is partially exposed on the surface), the thickness is 150 µm, and the basis weight is 20 g / m 2. (A nonwoven fabric was prepared by a usual dry method), and a breathable film was obtained in the same manner as in Example 1. The obtained breathable film showed the same good physical properties as in Example 1.

実施例3 不織布として、ポリプロピレン(融点165℃)不織布
(旭化成(株)製ポリプロスパンボンドP1015)をエチ
レン−ブテン−1共重合体(融点115℃、密度0.900g/cm
3)のキシレン溶液へ浸漬させて表面にエチレン−ブテ
ン−1共重合体を5重量%コーティングした。厚さ200
μm、坪量20g/m2のものを使用した以外は実施例1と同
様にして通気性フィルムを得た。得られた通気性フィル
ムは表1に示すように良好な物性を示した。
Example 3 As a nonwoven fabric, a polypropylene (melting point: 165 ° C.) nonwoven fabric (PolyProspan Bond P1015 manufactured by Asahi Kasei Corporation) was used as an ethylene-butene-1 copolymer (melting point: 115 ° C., density: 0.900 g / cm).
3 ) The surface was coated with 5% by weight of an ethylene-butene-1 copolymer by dipping in the xylene solution. Thickness 200
A breathable film was obtained in the same manner as in Example 1, except that a film having a thickness of 20 μm and a basis weight of 20 g / m 2 was used. The obtained breathable film showed good physical properties as shown in Table 1.

実施例4 不織布として、ポリエチレン(住友化学工業(株)
製、スミカセン−L FA202−0、融点124℃)35重量
%、ナイロン(ユニチカ(株)製、ナイロン6 A1030B
RT、融点215℃)60重量%およびエチレン・アクリル酸
エステル・無水マレイン酸三元共重合体(住化シーディ
ーエフ化学(有)販売、ボンダイン FX8000)5重量%
を溶融混練して得られる組成物を用い、特開平1−1561
4号公報の実施例に記載された方法(ただし、交絡・乾
燥後、線圧40kg/cm温度130℃の条件でロールによる押圧
処理を行なった)で得られた厚さ200μm、坪量25g/m2
の不織布(繊維繊度2デニール)を使用した以外は実施
例1と同様にして通気性フィルムを得た。得られた通気
性フィルムは表1に示すように良好な物性を示した。
Example 4 As a nonwoven fabric, polyethylene (Sumitomo Chemical Co., Ltd.)
35% by weight of Sumikasen-L FA202-0, melting point 124 ° C), nylon (Nylon 6 A1030B, manufactured by Unitika Ltd.)
RT, melting point 215 ° C) 60% by weight and ethylene / acrylic acid ester / maleic anhydride terpolymer (sold by Sumika CDF Chemical Co., Ltd., Bondine FX8000) 5% by weight
Using a composition obtained by melt-kneading
The thickness described in the method described in the example of Japanese Patent Publication No. 4 (except for the entanglement and drying, followed by pressing with a roll under the condition of a linear pressure of 40 kg / cm and a temperature of 130 ° C.), a thickness of 200 μm, and a grammage of 25 g / m 2
A non-woven fabric (fiber fineness: 2 deniers) was used in the same manner as in Example 1 to obtain a breathable film. The obtained breathable film showed good physical properties as shown in Table 1.

実施例5 熱可塑性樹脂として線状低密度ポリエチレン(住友化
学工業(株)製スミカセン α CS3003、密度0.932g/c
m3)、充填剤として二酸化チタン(デュポン社製 R10
1)を使用し表1に示した加工条件とした以外は実施例
1と同様にして通気性フィルムを得た。得られた通気性
フィルムは表1に示したように良好な物性を示した。
Example 5 As a thermoplastic resin, a linear low-density polyethylene (Sumikacene α CS3003 manufactured by Sumitomo Chemical Co., Ltd., density 0.932 g / c)
m 3 ), titanium dioxide (R10 manufactured by DuPont)
An air-permeable film was obtained in the same manner as in Example 1 except that the processing conditions shown in Table 1 were used using 1). The obtained breathable film showed good physical properties as shown in Table 1.

比較例1 不織布を使用せず表1に示した延伸条件で加工した以
外は実施例1と同様にして通気性フィルムを得た。得ら
れた通気性フィルムは引張強度や耐水性が著しく低い上
に延伸ムラが多かった。
Comparative Example 1 A breathable film was obtained in the same manner as in Example 1, except that processing was performed under the stretching conditions shown in Table 1 without using a nonwoven fabric. The obtained breathable film had remarkably low tensile strength and water resistance, and also had many stretching irregularities.

比較例2 充填剤として炭酸カルシウム(白石カルシウム(株)
製ホワイトンSSB(赤))を40重量部使用した以外は実
施例1と同様にして通気性フィルムを得た。得られた通
気性フィルムは表1に示すように通気性が著しく低かっ
た。
Comparative Example 2 Calcium carbonate (Shiroishi Calcium Co., Ltd.)
Except that 40 parts by weight of Whiten SSB (red) manufactured by Tokyo Gas Co., Ltd.) was used, a breathable film was obtained in the same manner as in Example 1. As shown in Table 1, the obtained air-permeable film had extremely low air permeability.

比較例3 熱可塑性樹脂として高圧法低密度ポリエチレン(住友
化学工業(株)製、スミカセンF208−0、密度0.922g/c
m3)100重量部と充填剤として炭酸カルシウム(白石カ
ルシウム(株)製ホワイトンSSB(赤))を500重量部使
用した以外は実施例1と同様にしてフィルム加工を行な
ったが、延伸加工時に樹脂組成物側が破断し通気性フィ
ルムを得ることができなかった。
Comparative Example 3 As a thermoplastic resin, a high-pressure method low-density polyethylene (Sumikasen F208-0, manufactured by Sumitomo Chemical Co., Ltd., density 0.922 g / c)
m 3 ) A film was processed in the same manner as in Example 1 except that 100 parts by weight and 500 parts by weight of calcium carbonate (Whiten SSB (red) manufactured by Shiraishi Calcium Co., Ltd.) were used as a filler, but stretching was performed. Sometimes, the resin composition side was broken, and a breathable film could not be obtained.

比較例4 不織布としてポリエステル(融点257℃)繊維から成
るものを使用した以外は実施例1と同様にして通気性フ
ィルムを得た。得られた通気性フィルムは表1に示すよ
うに不織布とフィルムの密着性が著しく低かった。
Comparative Example 4 A breathable film was obtained in the same manner as in Example 1 except that a nonwoven fabric made of polyester (melting point 257 ° C.) fiber was used. As shown in Table 1, the obtained breathable film had remarkably low adhesion between the nonwoven fabric and the film.

比較例5 樹脂組成物のラミネート加工時の温度を160℃にした
こと以外は実施例1と同様にして通気性フィルムを得
た。得られた通気性フィルムは表1に示すように不織布
と樹脂組成物との密着性が著しく低かった。
Comparative Example 5 A breathable film was obtained in the same manner as in Example 1 except that the temperature at the time of laminating the resin composition was 160 ° C. As shown in Table 1, the obtained breathable film had remarkably low adhesiveness between the nonwoven fabric and the resin composition.

比較例6 熱可塑性樹脂として線状低密度ポリエチレン(住友化
学工業(株)製エクセレンVL VL200、密度0.900g/c
m3)75重量%使用した以外は実施例1と同様にして通気
性フィルムを得た。得られた通気性フィルムは表1に示
すように通気性がかなり低く延伸ムラも多かった。
Comparative Example 6 Linear low density polyethylene (Excellen VL VL200 manufactured by Sumitomo Chemical Co., Ltd., density 0.900 g / c) was used as the thermoplastic resin.
m 3 ) A breathable film was obtained in the same manner as in Example 1 except that 75% by weight was used. As shown in Table 1, the obtained air-permeable film had considerably low air-permeability, and also had many stretching irregularities.

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】熱可塑性樹脂100重量部と充填剤50〜400重
量部からなる樹脂組成物を厚さ10μm〜400μmの不織
布上に溶融ラミネートした後、該不織布と同時に一軸ま
たは二軸に1.1〜3.0倍の倍率で延伸する方法において、
該不織布が40℃より高く、樹脂組成物の溶融ラミネート
温度より50℃以上低い融点を持つ樹脂成分を含むもので
あることを特徴とする通気性フィルムの製造方法。
1. A resin composition comprising 100 parts by weight of a thermoplastic resin and 50 to 400 parts by weight of a filler is melt-laminated on a nonwoven fabric having a thickness of 10 μm to 400 μm. In the method of stretching at a magnification of 3.0 times,
A method for producing a breathable film, characterized in that the nonwoven fabric contains a resin component having a melting point higher than 40 ° C and lower than the melting lamination temperature of the resin composition by 50 ° C or more.
【請求項2】不織布が2種類以上の樹脂成分より成り、
樹脂成分には40℃より高く、樹脂組成物の溶融ラミネー
ト温度より50℃以上低い融点を持つ樹脂成分を少なくと
も1種類以上含み、かつ不織布の表面の一部または全部
が少なくとも該樹脂成分であることを特徴とする特許請
求範囲第一項記載の通気性フィルムの製造方法。
2. The nonwoven fabric comprises two or more resin components,
The resin component contains at least one resin component having a melting point higher than 40 ° C. and lower than the melting lamination temperature of the resin composition by 50 ° C. or more, and at least a part or all of the surface of the nonwoven fabric is the resin component. The method for producing a breathable film according to claim 1, wherein:
【請求項3】不織布が芯層と鞘層を持つ繊維より成り、
少なくとも最外層の鞘層が40℃より高く樹脂組成物の溶
融ラミネート温度より50℃以上低い融点を持つ樹脂から
なることを特徴とする特許請求範囲第一項記載の通気性
フィルムの製造方法。
3. A nonwoven fabric comprising a fiber having a core layer and a sheath layer,
The method for producing a breathable film according to claim 1, wherein at least the outermost sheath layer is made of a resin having a melting point higher than 40 ° C and lower than the melting lamination temperature of the resin composition by 50 ° C or more.
【請求項4】熱可塑性樹脂が一種または二種以上の樹脂
よりなり、密度が0.920g/cm3以上である樹脂を40重量%
以上含むことを特徴とする特許請求範囲第一項記載の通
気性フィルムの製造方法。
4. The method according to claim 1, wherein the thermoplastic resin comprises one or more resins and has a density of 0.920 g / cm 3 or more by 40% by weight.
The method for producing a breathable film according to claim 1, wherein the method includes the above.
JP9973889A 1989-04-18 1989-04-18 Method for producing breathable film Expired - Fee Related JP2737236B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9973889A JP2737236B2 (en) 1989-04-18 1989-04-18 Method for producing breathable film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9973889A JP2737236B2 (en) 1989-04-18 1989-04-18 Method for producing breathable film

Publications (2)

Publication Number Publication Date
JPH02276636A JPH02276636A (en) 1990-11-13
JP2737236B2 true JP2737236B2 (en) 1998-04-08

Family

ID=14255370

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Link
JP (1) JP2737236B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5509142A (en) * 1993-06-30 1996-04-23 Kimberly-Clark Corporation Raised arm coveralls
GB2285411B (en) * 1993-12-22 1997-07-16 Kimberly Clark Co Process of manufacturing a water-based adhesive bonded, solvent resistant protective laminate
US5487189A (en) * 1994-03-16 1996-01-30 Kimberly-Clark Corporation Coveralls having reduced seams and seamless shoulder construction and method of manufacture
US5770529A (en) * 1995-04-28 1998-06-23 Kimberly-Clark Corporation Liquid-distribution garment
ES2151661T3 (en) * 1995-05-02 2001-01-01 Kimberly Clark Co LAMINATES OF FILM AND NON-WOVEN FABRIC.
US5865926A (en) * 1996-02-15 1999-02-02 Clopay Plastic Products Company, Inc. Method of making a cloth-like microporous laminate of a nonwoven fibrous web and thermoplastic film having air and moisture vapor permeabilities with liquid-barrier properties
EP0950512B1 (en) * 1998-01-27 2002-06-12 Reifenhäuser GmbH & Co. Maschinenfabrik Method for producing a laminated web
DE19838507C2 (en) * 1998-08-25 2002-04-25 Borealis Gmbh Schwechat Mannsw Extrusion coated nonwoven webs
DE10023615A1 (en) * 2000-05-16 2001-11-22 Reifenhaeuser Masch Process and plant for producing a water vapor permeable laminate web
ITPS20020023A1 (en) * 2002-11-14 2004-05-15 Cl Com Srl Advanced Technology PARTIAL BODY PROTECTION CLOTHES AGAINST BIOLOGICAL AGENTS.

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