JPH0159105B2 - - Google Patents
Info
- Publication number
- JPH0159105B2 JPH0159105B2 JP11754085A JP11754085A JPH0159105B2 JP H0159105 B2 JPH0159105 B2 JP H0159105B2 JP 11754085 A JP11754085 A JP 11754085A JP 11754085 A JP11754085 A JP 11754085A JP H0159105 B2 JPH0159105 B2 JP H0159105B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- porous resin
- laminated film
- resin laminated
- porous
- 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
Links
- 239000011347 resin Substances 0.000 claims description 28
- 229920005989 resin Polymers 0.000 claims description 28
- 239000000843 powder Substances 0.000 claims description 19
- 230000035699 permeability Effects 0.000 claims description 15
- 239000010410 layer Substances 0.000 claims description 13
- 229920000098 polyolefin Polymers 0.000 claims description 13
- -1 polyethylene Polymers 0.000 claims description 12
- 239000004698 Polyethylene Substances 0.000 claims description 10
- 229920000573 polyethylene Polymers 0.000 claims description 10
- 239000002344 surface layer Substances 0.000 claims description 8
- 229920001903 high density polyethylene Polymers 0.000 claims description 7
- 239000004700 high-density polyethylene Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 6
- 230000005484 gravity Effects 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 4
- 239000002390 adhesive tape Substances 0.000 description 12
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- 239000007788 liquid Substances 0.000 description 7
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 238000002834 transmittance Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000428 dust Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 210000005069 ears Anatomy 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
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
〔産業上の利用分野〕
本発明は、つかいすておむつ、生理用ナプキ
ン、電解隔膜等に有用な表面強度の優れる通気性
を有する多孔性樹脂積層フイルムに関する。
〔従来技術〕
生理用ナプキン、つかいすておむつにおいて、
通気性と防水性を有するポリオレフイン系多孔樹
脂フイルムが防漏材として使用されている。
かかる多孔樹脂フイルムは、高密度ポリエチレ
ン、線状ポリエチレンまたは両者の混合物を樹脂
素材とし、これに炭酸カルシウム、酸化チタン、
焼成クレイ、けいそう土等の無機微細粉末、必要
によりポリエチレンワツクス、液状ブタジエンゴ
ム、液状イソブチレンゴム、液状ポリエチレンワ
ツクス、液状水添ヒマシ油、等の柔軟性改良剤を
配合した組成物を押出機を用いてフイルム状に溶
融成形後、マンドレル、ロール群の周速差を利用
した延伸装置、またはテンターを用いて延伸成形
することにより製造されている(特開昭57−
47334号、同57−203520号、同58−15538号、同58
−149925号、同58−149303号、同59−62117号、
同59−140235号、同60−6442号)。
〔従来技術の問題点〕
この多孔樹脂フイルムは無機微細粉末を核とし
て微細な連続空孔を多数有し、表面には大気に連
通した空隙を有する通気性に富む単層の1軸延伸
フイルムまたは2軸延伸フイルムで、つかいすて
おむつの防水カバーシートとして有用である。
この多孔樹脂フイルムをつかいすておむつの防
水カバーシートとして用いるとき、表面に離型紙
を備えた両面粘着テープが止め具として用いられ
赤ちやんの股につかいすておむつを装着した後、
両面粘着テープの表面の離型紙を引き剥し、露呈
した粘着剤で貼着してつかいすておむつを固定す
る。
この粘着テープを多孔樹脂フイルムの誤つた位
置に貼合した場合または貼合した位置を少しずら
せたいとき、粘着テープを貼着しなおすためにつ
かいすておむつより剥離すると、従来の多孔樹脂
2軸延伸フイルムは表面に無機微細粉末が突出、
遊離もしくは樹脂フイルム基材に付着して露出し
ており、前記空孔が円形ないし楕円状であり無機
微細粉末が脱落しやすくなつているので、この無
機微細粉末が粘着テープの粘着面に移動し、粘着
テープの粘着力を低下させる原因となつたり、多
孔樹脂フイルムの表面強度が低いためにフイルム
表面が紙ムケ状に剥離したりする問題がある。
一方、一軸延伸フイルムは、空孔が長尺状であ
り、延伸面積倍率も2軸延伸フイルムのそれより
小さいので無機微細粉末の脱落も2軸延伸フイル
ムより少なく、かつ、表面強度も2軸延伸フイル
ムのそれより強い利点があるが、方向性があると
ともに抗クリープ性に乏しく、おむつカバーが使
用時に伸びきつてゆるんでしまい、防漏性を満足
させることができない。特に引張り破断伸びが
500%を超えるものは好ましくない。
〔問題点を解決するための具体的手段〕
本発明においては、多孔樹脂フイルムを2軸延
伸フイルムと一軸延伸フイルムの複層構造とし、
基材層の2軸延伸フイルムで抗クリープ性を付与
し、粘着テープが貼着される表面層を無機微細粉
末含有多孔樹脂一軸延伸フイルムとすることによ
り表面強度を向上させるとともに粘着テープへ移
行する無機微細粉末の量を低下させることにより
前記問題点を解決するものである。
即ち、本発明は、無機微細粉末を50〜75重量%
の割合で含有するポリオレフインの2軸延伸多孔
フイルム(A)を基材層として含み、無機微細粉末を
55〜75重量%の割合で含有するポリオレフインの
一軸延伸多孔フイルムよりなる表面層(B)とを含む
多孔性樹脂積層フイルムであつて、この多孔性樹
脂積層フイルムの20℃における透気度は40〜7000
秒であり、20℃における透湿度は100〜10000g/
m2・24時間1気圧であることを特徴とする多孔性
樹脂積層フイルムを提供するものである。
(樹脂)
本発明の実施において、各(A)層および(B)層の樹
脂素材としてポリオレフインとしては高密度ポリ
エチレン、線状ポリエチレン、低密度ポリエチレ
ン、ポリプロピレン、エチレン・プロピレン共重
合体、ポリブテン等のポリオレフインまたはこれ
ら2種以上の混合物があげられ、特に、つかいす
ておむつの防水カバーシートを考えた場合、比重
が0.92〜0.97、メルトインデツクス(MI)が0.06
〜1g/10分(190℃)の高密度ポリエチレン65
〜30重量%と、比重が0.91〜0.94、MIが0.1〜10
g/10分の線状ポリエチレン35〜70重量%との混
合物を用いたときは、得られる多孔樹脂フイルム
の風合、肌ざわりがよい。
(無機微細粉末)
無機微細粉末としては、平均粒径が20ミクロン
以下、好ましくは3ミクロン以下のものが用いら
れ、炭酸カルシウム、けいそう土、焼成クレイ、
けい酸アルミニウム、タルク等があげられる。
(任意成分)
ポリオレフイン、無機微細粉末の他に必要によ
り安定剤、顔料、分散剤、可塑剤、帯電防止剤、
液状ブタジエンゴム、ポリエチレンワツクス、液
状イソブチレンゴム、アタツクポリプロピレン、
ジブチルフタレート、液状水添ヒマシ油等を配合
してよい。
(積層フイルム)
多孔積層フイルムは、無機微細粉末を50〜75重
量%含有するポリオレフイン(A)を押出機で溶融混
練し、ダイよりシート状に押し出し、ポリオレフ
インの融点より低い温度にシートを冷却後、延伸
できる温度に加熱し(通常、融点より3〜35℃低
い温度)、ロール群の周速差を利用して縦方向に
1.3〜7倍、好ましくは1.8倍延伸した後、この縦
延伸フイルムの片面または両面に、無機微細粉末
を55〜75重量%含有するポリオレフイン(B)の溶融
フイルムを溶融積層し、この積層フイルムをポリ
オレフインの融点より低い温度に冷却後、テンタ
ーを用いて1.2〜10倍、好ましくは1.2〜3.5倍横方
向に延伸し、ついで必要により熱処理したのち、
冷却し、耳部をスリツトすることにより製造され
る。
他の製造例としては、基層フイルムおよび/ま
たは表面層フイルムを樹脂や無機微細粉末の種類
や配合量を変えた組成物の積層フイルムとして製
造してもよい。
この多孔樹脂積層フイルムは、JIS Z−0208に
より20℃で測定した透湿度が100〜10000g/m2・
24時間・1気圧、好ましくは200〜5000g/m2・
24時間・1気圧であり、次の方法で測定した20℃
における透気度が40〜7000秒、好ましくは100〜
4000秒である。
透気度の測定法
JIS P−8117に準拠して作られた王研式透気度
(平滑度試験機(旭精工製)を用いて測定)
透気度、透湿度が前範囲を外れると、この多孔
性積層フイルムをおむつの防水カバーや使いすて
生理用ナプキンの防漏材として用いたとき、むれ
がおきやすいか、防液性がない。
(効果)
本発明の多孔性積層フイルムは、2軸延伸フイ
ルム基材層(A)を含むので強度バランスに優れ、ク
リープ伸びや引き裂きが少ない。また、表面層の
一軸延伸フイルム(B)の無機微細粉末が突出し、マ
ツト調(粗面)となつているので、この多孔性樹
脂積層フイルムをエンポス加工したものは外観が
布に近く、かつ、手触りが良好である。また、突
出した(B)層の無機微細粉末は表面層(B)が一軸延伸
フイルムとなつているのでフイルム表面より脱落
しにくくなつており、又、表面のフイブリル化の
程度が低い為2軸延伸フイルムと較べ表面強度が
強く、表面が紙ムケ状に剥離してくることがな
く、紙粉トラブル(粘着テープの再接着不良)が
生じ難い。
実施例 1
(1) 密度0.92g/cm3、メルトインデツクス1.0
g/10分の線状ポリエチレン20重量部、密度
0.95g/cm3、メルトインデツクス0.08g/10分
の高密度ポリエチレン20重量部および平均粒径
1.8ミクロンの炭酸カルシウム60重量部よりな
る樹脂組成物(A)を押出機を用いて溶融混練し、
220℃でダイよりシート状に押し出し、このシ
ートを70℃まで冷却後、110℃まで加熱し、ロ
ール群の周速差を利用して縦方向に2.5倍延伸
し、縦延伸フイルムを得た。
(2) 密度0.92g/cm3、メルトインデツクス1.0
g/10分の線状ポリエチレン20重量部、密度
0.95g/cm3、メルトインデツクス0.08g/10分
の高密度ポリエチレン20重量部および平均粒径
1.8ミクロンの炭酸カルシウム60重量部よりな
る樹脂組成物(B)を押出機を用いて溶融混練し、
これをダイよりシート状に押し出し、前記(1)で
得た縦延伸フイルムの両面に積層し、60℃まで
冷却し、ついで加熱オーブン内に導き、約114
℃まで加熱した後、テンターを用いて横方向に
2.5倍延伸し、これを約118℃で熱処理した後、
50℃まで冷却し、耳部をスリツトして(B)/(A)/
(B)の各肉厚が10μ/40μ/10μの3層積層フイル
ムを得た。
この積層フイルムの透気度(20℃)、透湿度
(20℃)紙粉トラブル度およびクリープ度(JIS
P−8132で測定した引張り破断伸び。)を表1に
示す。
なお、紙粉トラブル度は次の方法により測定し
た。
粘着テープ“セロフアンテープ”(ニチバン製
商品名、LP−18)をフイルム面に貼着し親指の
腹で5回こすつた後、テンシロン(東洋ポールド
ボーウイン製)で200mm/分の速度で粘着テープ
を剥離した。
この粘着テープの透光量をカラーメーター(ス
ガ試験機製)で測定した。
予め、粘着する前の粘着テープの透光量をブラ
ンク値として測定しておき、これで前記値を除し
たものを透光率とした(値の大きいものほど紙粉
トラブルは少ない)。
透光率が80%以上のものは透光率の他に若干問
題有りと付記し、また70%以下のものは不良と付
記した。
また、剥離の時多孔樹脂フイルム表面層が破断
して透光率の測定不能なものは紙ムケ不良と記し
た。
実施例2〜7、比較例1〜3
各組成物の割合または延伸倍率を表1に示すよ
うに変化、または各層の肉厚を同表に示すように
する他は、実施例1と同様にして2層または3層
積層フイルムを得た。
これら積層フイルムの透気度、透湿度、紙粉ト
ラブル度およびクリープ度を同表に示す。
比較例 4
密度0.92g/cm3、メルトインデツクス1.0g/
10分の線状ポリエチレン20重量部、密度0.95g/
cm3、メルトインデツクス0.08g/10分の高密度ポ
リエチレン20重量部および平均粒径1.8ミクロン
の炭酸カルシウム60重量部よりなる樹脂組成物(A)
を押出機を用いて溶融混練し、220℃でダイより
シート状に押し出し、このシートを70℃まで冷却
した。
このシートを110℃まで加熱し、ロール群の周
速差を利用して縦方向に2.5倍延伸し、縦延伸フ
イルムを得た。
この一軸延伸フイルムの物性を表1に示す。
比較例 5
上記比較例4の縦延伸フイルムを更に加熱オー
ブン内に導き、約114℃まで加熱した後、テンタ
ーを用いて横方向に2倍延伸し、これを118℃で
熱処理した後、50℃まで冷却し、耳部をスリツト
して50μの2軸延伸フイルムを得た。
このフイルムの物性を表1に示す。
[Industrial Field of Application] The present invention relates to a porous resin laminated film having excellent surface strength and air permeability, useful for disposable diapers, sanitary napkins, electrolytic diaphragms, etc. [Prior art] In sanitary napkins and disposable diapers,
Polyolefin porous resin film, which has breathability and waterproof properties, is used as a leak-proof material. Such porous resin film uses high-density polyethylene, linear polyethylene, or a mixture of both as a resin material, and contains calcium carbonate, titanium oxide,
Extrusion of a composition containing inorganic fine powder such as fired clay or diatomaceous earth, and if necessary, a flexibility improver such as polyethylene wax, liquid butadiene rubber, liquid isobutylene rubber, liquid polyethylene wax, liquid hydrogenated castor oil, etc. It is manufactured by melt-forming into a film using a machine, and then stretching and forming using a mandrel, a stretching device that utilizes the peripheral speed difference between a group of rolls, or a tenter.
No. 47334, No. 57-203520, No. 58-15538, No. 58
−149925, No. 58-149303, No. 59-62117,
59-140235, 60-6442). [Problems with the prior art] This porous resin film has a large number of fine continuous pores with a core of inorganic fine powder, and a highly air permeable single layer uniaxially stretched film with voids communicating with the atmosphere on the surface. This biaxially stretched film is useful as a waterproof cover sheet for disposable diapers. When this porous resin film is used as a waterproof cover sheet for disposable diapers, a double-sided adhesive tape with release paper on the surface is used as a fastener, and after the diaper is attached to the baby's crotch,
Peel off the release paper on the surface of the double-sided adhesive tape and use the exposed adhesive to fix the disposable diaper. When this adhesive tape is attached to the wrong position of the porous resin film or when you want to slightly shift the attached position, you can use it to reapply the adhesive tape and peel it off from the diaper. The stretched film has fine inorganic powder protruding from the surface.
The pores are either free or attached to the resin film base material and exposed, and the pores are circular or elliptical, making it easy for the inorganic fine powder to fall off, so this inorganic fine powder moves to the adhesive surface of the adhesive tape. However, since the surface strength of the porous resin film is low, the surface of the film may peel off like paper flakes. On the other hand, in a uniaxially stretched film, the pores are long and the stretching area ratio is smaller than that of a biaxially stretched film, so the amount of inorganic fine powder falling off is less than that of a biaxially stretched film, and the surface strength is also lower than that of a biaxially stretched film. Although it has stronger advantages than film, it has directionality and poor creep resistance, and the diaper cover stretches and loosens during use, making it impossible to satisfy leak-proof properties. Especially the tensile elongation at break
Anything over 500% is not desirable. [Specific means for solving the problem] In the present invention, the porous resin film has a multilayer structure of a biaxially stretched film and a uniaxially stretched film,
The base layer is a biaxially stretched film that provides creep resistance, and the surface layer to which the adhesive tape is attached is a porous resin uniaxially stretched film containing inorganic fine powder to improve surface strength and transfer to the adhesive tape. This problem is solved by reducing the amount of inorganic fine powder. That is, the present invention uses 50 to 75% by weight of inorganic fine powder.
The base layer includes a biaxially stretched porous film (A) of polyolefin containing a proportion of
A porous resin laminated film comprising a surface layer (B) consisting of a uniaxially stretched porous film containing polyolefin in a proportion of 55 to 75% by weight, the porous resin laminated film having an air permeability of 40 at 20°C. ~7000
seconds, and the moisture permeability at 20℃ is 100 to 10,000 g/
The present invention provides a porous resin laminated film characterized by a pressure of 1 atm for 24 hours. (Resin) In the practice of the present invention, polyolefins such as high-density polyethylene, linear polyethylene, low-density polyethylene, polypropylene, ethylene-propylene copolymer, polybutene, etc. are used as the resin material for each (A) layer and (B) layer. Examples include polyolefin or a mixture of two or more of these, and in particular, when considering waterproof cover sheets for disposable diapers, polyolefins have a specific gravity of 0.92 to 0.97 and a melt index (MI) of 0.06.
~1g/10min (190℃) high density polyethylene 65
~30% by weight, specific gravity 0.91-0.94, MI 0.1-10
When a mixture with 35 to 70% by weight of linear polyethylene of 35 to 70 g/10 min is used, the resulting porous resin film has good texture and touch. (Inorganic fine powder) As the inorganic fine powder, those having an average particle size of 20 microns or less, preferably 3 microns or less are used, and include calcium carbonate, diatomaceous earth, calcined clay,
Examples include aluminum silicate and talc. (Optional ingredients) In addition to polyolefin and inorganic fine powder, stabilizers, pigments, dispersants, plasticizers, antistatic agents,
Liquid butadiene rubber, polyethylene wax, liquid isobutylene rubber, attack polypropylene,
Dibutyl phthalate, liquid hydrogenated castor oil, etc. may be blended. (Laminated film) Porous laminated film is produced by melt-kneading polyolefin (A) containing 50 to 75% by weight of inorganic fine powder in an extruder, extruding it into a sheet from a die, and cooling the sheet to a temperature lower than the melting point of the polyolefin. , heated to a temperature that allows stretching (usually 3 to 35 degrees Celsius lower than the melting point), and then stretched in the longitudinal direction using the difference in circumferential speed of the roll group.
After stretching 1.3 to 7 times, preferably 1.8 times, a molten film of polyolefin (B) containing 55 to 75% by weight of inorganic fine powder is melt-laminated on one or both sides of this longitudinally stretched film, and this laminated film is After cooling to a temperature lower than the melting point of the polyolefin, it is stretched 1.2 to 10 times, preferably 1.2 to 3.5 times in the transverse direction using a tenter, and then heat treated if necessary.
Manufactured by cooling and slitting the ears. As another manufacturing example, the base layer film and/or the surface layer film may be manufactured as a laminated film of a composition in which the type and blending amount of resin or inorganic fine powder are changed. This porous resin laminated film has a moisture permeability of 100 to 10,000 g/m 2 when measured at 20°C according to JIS Z-0208.
24 hours/1 atm, preferably 200-5000g/ m2 .
24 hours, 1 atm, 20℃ measured by the following method
The air permeability is 40~7000 seconds, preferably 100~
It is 4000 seconds. Air permeability measurement method Oken type air permeability made in accordance with JIS P-8117 (measured using a smoothness tester (manufactured by Asahi Seiko)) If the air permeability and moisture permeability are out of the previous range When this porous laminated film is used as a waterproof cover for diapers or as a leak-proof material for disposable sanitary napkins, it tends to get stuffy or lacks liquid-proof properties. (Effects) Since the porous laminated film of the present invention includes the biaxially stretched film base layer (A), it has excellent strength balance and has little creep elongation or tearing. In addition, the inorganic fine powder of the uniaxially stretched film (B) in the surface layer protrudes and has a matte-like (rough surface), so the embossing process of this porous resin laminated film has an appearance similar to that of cloth, and Good to the touch. In addition, since the surface layer (B) is a uniaxially stretched film, the inorganic fine powder of the protruding layer (B) is less likely to fall off from the film surface, and the degree of fibrillation on the surface is low, so it is difficult to fall off from the surface of the film. It has a stronger surface strength than a stretched film, the surface does not peel off like paper flakes, and paper dust problems (poor adhesive tape re-adhesion) are less likely to occur. Example 1 (1) Density 0.92g/cm 3 , Melt index 1.0
g/10 min linear polyethylene 20 parts by weight, density
20 parts by weight of high-density polyethylene of 0.95 g/cm 3 , melt index 0.08 g/10 min and average particle size
A resin composition (A) consisting of 60 parts by weight of 1.8 micron calcium carbonate is melt-kneaded using an extruder,
It was extruded into a sheet through a die at 220°C, cooled to 70°C, heated to 110°C, and stretched 2.5 times in the longitudinal direction using the difference in circumferential speed between the roll groups to obtain a longitudinally stretched film. (2) Density 0.92g/cm 3 , Melt index 1.0
g/10 min linear polyethylene 20 parts by weight, density
20 parts by weight of high-density polyethylene of 0.95 g/cm 3 , melt index 0.08 g/10 min and average particle size
A resin composition (B) consisting of 60 parts by weight of 1.8 micron calcium carbonate is melt-kneaded using an extruder,
This was extruded into a sheet form through a die, laminated on both sides of the longitudinally stretched film obtained in (1) above, cooled to 60°C, then introduced into a heating oven,
After heating to ℃, crosswise using a tenter.
After stretching 2.5 times and heat treating it at about 118℃,
Cool to 50℃ and slit the ears (B)/(A)/
A three-layer laminated film (B) having thicknesses of 10μ, 40μ, and 10μ was obtained. This laminated film has air permeability (20℃), moisture permeability (20℃), paper powder trouble level, and creep degree (JIS
Tensile elongation at break measured with P-8132. ) are shown in Table 1. The degree of paper dust trouble was measured by the following method. Adhesive tape "Cellophane Tape" (trade name, LP-18 manufactured by Nichiban) was applied to the film surface, rubbed 5 times with the pad of the thumb, and then rubbed at a speed of 200 mm/min with Tensilon (manufactured by Toyo Paul de Bowin). Peel off the adhesive tape. The amount of light transmitted through this adhesive tape was measured using a color meter (manufactured by Suga Test Instruments). The amount of light transmitted through the adhesive tape before adhesion was measured as a blank value, and the value divided by this value was defined as the light transmittance (the larger the value, the less paper dust trouble occurs). Items with a light transmittance of 80% or more were noted as having some problems in addition to the light transmittance, and items with a light transmittance of 70% or less were noted as defective. In addition, when the surface layer of the porous resin film was broken during peeling and the light transmittance could not be measured, it was described as a paper smudge defect. Examples 2 to 7, Comparative Examples 1 to 3 The procedure was the same as in Example 1, except that the ratio of each composition or the stretching ratio was changed as shown in Table 1, or the thickness of each layer was changed as shown in Table 1. A two-layer or three-layer laminated film was obtained. The air permeability, moisture permeability, paper dust trouble level, and creep degree of these laminated films are shown in the same table. Comparative example 4 Density 0.92g/cm 3 , Melt index 1.0g/
20 parts by weight of 10-minute linear polyethylene, density 0.95 g/
Resin composition ( A ) consisting of 20 parts by weight of high-density polyethylene with a melt index of 0.08 g/10 min and 60 parts by weight of calcium carbonate with an average particle size of 1.8 microns.
were melt-kneaded using an extruder, extruded into a sheet from a die at 220°C, and this sheet was cooled to 70°C. This sheet was heated to 110° C. and stretched 2.5 times in the longitudinal direction using the difference in peripheral speed between the roll groups to obtain a longitudinally stretched film. Table 1 shows the physical properties of this uniaxially stretched film. Comparative Example 5 The longitudinally stretched film of Comparative Example 4 above was further guided into a heating oven, heated to about 114°C, then stretched twice in the transverse direction using a tenter, heat-treated at 118°C, and then heated to 50°C. The film was cooled to a temperature of 50 μm, and the edges were slit to obtain a 50 μm biaxially stretched film. Table 1 shows the physical properties of this film.
【表】【table】
Claims (1)
るポリオレフインの2軸延伸多孔フイルム(A)を基
材層として含み、無機微細粉末を55〜75重量%の
割合で含有するポリオレフインの一軸延伸多孔フ
イルムよりなる表面層(B)とを含む多孔性樹脂積層
フイルムであつて、この多孔性樹脂積層フイルム
の20℃における透気度は40〜7000秒であり、20℃
における透湿度は100〜10000g/m2、24時間1気
圧であることを特徴とする多孔性樹脂積層フイル
ム。 2 JIS−P−8132にもとずいて20℃で測定した
引張り破断伸びが縦方向、横方向とも500%以下
であることを特徴とする特許請求の範囲第1項記
載の多孔性樹脂積層フイルム。 3 基材層(A)または表面層(B)の素材樹脂が、比重
0.92〜0.97、メルトインデツクス0.06〜1g/10
分の高密度ポリエチレン65〜30重量%と、比重
0.91〜0.94、メルトインデツクス0.1〜10g/10分
の線状ポリエチレン35〜70重量%との混合物であ
ることを特徴とする特許請求の範囲第1項記載の
多孔性樹脂積層フイルム。 4 フイルム(B)が延伸倍率1.2〜3.5倍の一軸延伸
フイルムであることを特徴とする特許請求の範囲
第1項記載の多孔性樹脂積層フイルム。[Claims] 1. A biaxially stretched porous film (A) of polyolefin containing 50 to 75% by weight of inorganic fine powder as a base layer; A porous resin laminated film comprising a surface layer (B) made of a uniaxially stretched porous film containing polyolefin, the porous resin laminated film has an air permeability of 40 to 7000 seconds at 20°C, and
A porous resin laminated film having a moisture permeability of 100 to 10,000 g/m 2 and a pressure of 1 atm for 24 hours. 2. The porous resin laminated film according to claim 1, characterized in that the tensile elongation at break measured at 20°C in accordance with JIS-P-8132 is 500% or less in both the longitudinal and transverse directions. . 3 The material resin of the base layer (A) or surface layer (B) has a specific gravity
0.92-0.97, melt index 0.06-1g/10
Min high density polyethylene 65-30% by weight, specific gravity
The porous resin laminated film according to claim 1, which is a mixture of 35 to 70% by weight of linear polyethylene with a melt index of 0.91 to 0.94 and a melt index of 0.1 to 10 g/10 min. 4. The porous resin laminated film according to claim 1, wherein the film (B) is a uniaxially stretched film with a stretching ratio of 1.2 to 3.5 times.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11754085A JPS61273941A (en) | 1985-05-30 | 1985-05-30 | Porous resin laminated film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11754085A JPS61273941A (en) | 1985-05-30 | 1985-05-30 | Porous resin laminated film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61273941A JPS61273941A (en) | 1986-12-04 |
JPH0159105B2 true JPH0159105B2 (en) | 1989-12-14 |
Family
ID=14714322
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11754085A Granted JPS61273941A (en) | 1985-05-30 | 1985-05-30 | Porous resin laminated film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61273941A (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3763652B2 (en) * | 1997-11-05 | 2006-04-05 | 花王株式会社 | Breathable film |
TW379272B (en) | 1998-03-05 | 2000-01-11 | Longmeng Environmental Papers | Method of manufacturing recycling papers |
CN1105636C (en) * | 1998-03-25 | 2003-04-16 | 香港商龙盟环保纸(集团)有限公司 | Manufacturing method of environmentally friendly paper |
JP4540888B2 (en) * | 2001-07-03 | 2010-09-08 | 三井化学株式会社 | Back sheet for water absorbent articles |
TWI331087B (en) | 2003-03-06 | 2010-10-01 | Sumitomo Chemical Co | Method for producing laminated porous polyolefin film and laminated porous polyolefin film |
WO2006125087A2 (en) * | 2005-05-18 | 2006-11-23 | Petoskey Plastics, Inc. | Vapor dispersible plastic film paint adherence and cling |
JP4686256B2 (en) * | 2005-05-25 | 2011-05-25 | 三菱樹脂株式会社 | Laminated porous film |
RU2008102735A (en) * | 2005-06-24 | 2009-07-27 | Тонен Кемикал Корпорейшн (Jp) | MULTI-LAYERED MICROPOROUS POLYETHYLENE MEMBRANE AND BATTERY SEPARATOR AND BATTERY USING THE MEMBRANE |
JP5461614B2 (en) | 2011-05-31 | 2014-04-02 | 株式会社Tbm | Manufacturing method of inorganic substance powder high-mixing thin film sheet |
CN108498845B (en) * | 2018-04-28 | 2020-12-15 | 青岛艾暖医疗科技有限公司 | High-comfort pain-relieving chitin sanitary pad and manufacturing method thereof |
-
1985
- 1985-05-30 JP JP11754085A patent/JPS61273941A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61273941A (en) | 1986-12-04 |
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