JPH02162008A - Manufacture of air-permeable composite sheet - Google Patents

Manufacture of air-permeable composite sheet

Info

Publication number
JPH02162008A
JPH02162008A JP63316293A JP31629388A JPH02162008A JP H02162008 A JPH02162008 A JP H02162008A JP 63316293 A JP63316293 A JP 63316293A JP 31629388 A JP31629388 A JP 31629388A JP H02162008 A JPH02162008 A JP H02162008A
Authority
JP
Japan
Prior art keywords
thermoplastic resin
base material
inorganic filler
porous base
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.)
Pending
Application number
JP63316293A
Other languages
Japanese (ja)
Inventor
Takefumi Sonoda
園田 武文
Shigenori Fujioka
藤岡 成典
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.)
Tosoh Corp
Original Assignee
Tosoh Corp
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 Tosoh Corp filed Critical Tosoh Corp
Priority to JP63316293A priority Critical patent/JPH02162008A/en
Publication of JPH02162008A publication Critical patent/JPH02162008A/en
Pending legal-status Critical Current

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  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Laminated Bodies (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)

Abstract

PURPOSE:To simultaneously perform both the production of porous thermoplastic resin film and its bonding to porous base material such as non-woven fabric or the like by a method wherein composition consisting of the thermoplastic resin, inorganic filler and liquid component, which stands against the heat having the specified temperature, is extrusion-laminated to the porous base material. CONSTITUTION:Both the bonding of composition consisting of thermoplastic resin, inorganic filler and liquid component, which stands against the heat having a temperature of 250 deg.C or higher, to porous base material and the production of porous thermoplastic resin film are simultaneously performed by extrusion-laminating the composition to the porous base material. As the thermoplastic resin, low density polyethylene, high density polyethylene or the like, the melt index of which is preferably 2 - 15 and which is preferably in the form of powder of 20- 200 mesh, is exampled. As the inorganic filler, calcium carbonate, barium sulface or the like, the mean particle diameter of which is preferably 1 - 10mum, is exemplified. As the liquid component, plasticizer or liquid hydrocarbon polymer, which stands against the heat having a temperature of 250 deg.C or higher, is used. As the porous base material, non-woven fabric, woven fabric or the like made of polyester or high density polyethylene, the void of which is preferably 95% or less, is cited. The preferable blending ratio is 20 - 300pts.wt. of the inorganic filler to 100pts.wt. of the thermoplastic resin.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は多孔性基材と熱可塑性樹脂フィルムとからなる
通気性調合シートの製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a method for manufacturing an air-permeable blended sheet comprising a porous base material and a thermoplastic resin film.

近年不織布等の多孔性基材と透水性、透湿性。In recent years, porous substrates such as non-woven fabrics and water permeability and moisture permeability.

通気性を調整する機能を有する、有孔フィルムを複合し
た通気性複合シートが広(利用される様になって来てい
る。代表的な例として使い捨ての紙おむつ、生理用品、
使い捨てカイロ、フィルター等が挙げられる。これらの
通気性複合シートの製造方法は2 PJ類の方法に大別
される。
Breathable composite sheets made of perforated films that have the function of adjusting breathability are becoming widely used. Typical examples include disposable diapers, sanitary products,
Examples include disposable warmers and filters. Methods for producing these breathable composite sheets are broadly classified into two PJ methods.

(1)無機系、有機系フィラーをブレンドしたフィルム
を延伸、あるいはフィラーを除去する等の方法であらか
じめ有孔化された、熱可塑性樹脂フィルムと多孔性基材
とを接合する方法 (2)熱可塑性樹脂フィルムと多孔性基材とを接合しそ
の後コロナ族7はあるいはニードルパンチ等の方法で熱
可塑性樹脂フィルムを有孔化する方法である。
(1) A method of bonding a porous base material to a thermoplastic resin film that has been made porous in advance by stretching a film blended with inorganic and organic fillers or removing the filler. (2) Heat This is a method in which a plastic resin film and a porous base material are joined together, and then the thermoplastic resin film is made porous by a method such as needle punching or the like.

いずれの製造方法も熱可塑性樹脂フィルムの有孔化工程
及びそれを多孔性基材に接合する接合工程の2工程に分
かれている。その為に品質管理上。
Both manufacturing methods are divided into two steps: a step of forming pores in the thermoplastic resin film and a bonding step of bonding it to a porous base material. For that reason, quality control.

工程管理上不利であるばかりでなく有孔化装置。Not only is it disadvantageous in terms of process control, but also the perforation equipment.

接合装置の2種類の装置が必要であるため設備投資が大
きく、また製品のコストダウンが難しい欠点がある。
Since two types of bonding devices are required, there is a drawback that the equipment investment is large and it is difficult to reduce the cost of the product.

[発明が解決しようとする課題] 本発明の目的は従来の方法では達成されなかった、熱可
塑性樹脂フィルムの有孔化と不織布等の多孔性基材との
接合を同時に行う方法を提供するものである。
[Problems to be Solved by the Invention] An object of the present invention is to provide a method for simultaneously making a thermoplastic resin film porous and bonding it to a porous substrate such as a nonwoven fabric, which has not been achieved by conventional methods. It is.

[課題を解決するための手段] 上記のような現状に鑑み、本発明者らは鋭意検討を重ね
た結果、熱可塑性樹脂、無機フィラー及び250℃以上
の耐熱性をもつ液状成分からなる組成物を多孔性基材に
押出ラミネートすることで接合と同時に熱可塑性樹脂フ
ィルムが有孔化することを見出し、本発明を完成するに
至った。
[Means for Solving the Problems] In view of the above-mentioned current situation, the present inventors have made extensive studies and have developed a composition consisting of a thermoplastic resin, an inorganic filler, and a liquid component having heat resistance of 250°C or higher. It was discovered that by extrusion laminating a thermoplastic resin film onto a porous substrate, the thermoplastic resin film becomes porous at the same time as bonding, and the present invention was completed.

以下本発明の詳細な説明する。The present invention will be explained in detail below.

ここで熱可塑性樹脂としては低密度ポリエチレン、高密
度ポリエチレン、ポリプロピレン、エチレン−酢酸ビニ
ル共重合体等のポリオレフィン樹脂及び、又は、これら
のブレンド体を挙げる事ができる。ドローダウン性、接
着性等の押出ラミネート加工性の点から通常押出ラミネ
ート用として用いられているメルトインデックス(Ml
)2〜15のものが好適であり、その形状は20〜20
0メツシユのパウダー状が好ましい。
Examples of the thermoplastic resin include polyolefin resins such as low density polyethylene, high density polyethylene, polypropylene, ethylene-vinyl acetate copolymer, and/or blends thereof. Melt index (Ml
) 2 to 15 are suitable, and the shape is 20 to 20
A powder form with 0 mesh is preferred.

無機フィラーとしては炭酸カルシウム、硫酸バリウム、
タルク、クレー、炭酸マグネシウム、炭酸バリウム、カ
オリン、シリカ、珪藻土、硫酸マグネシウム、硫酸カル
シウム、酸化亜鉛、水酸化マグネシウム、水酸化アルミ
ニウム、マイカ、アスベスト粉、ガラス粉、シラスバル
ーン、ゼオライト、珪酸白土等を挙げることができる。
Inorganic fillers include calcium carbonate, barium sulfate,
Talc, clay, magnesium carbonate, barium carbonate, kaolin, silica, diatomaceous earth, magnesium sulfate, calcium sulfate, zinc oxide, magnesium hydroxide, aluminum hydroxide, mica, asbestos powder, glass powder, shirasu balloon, zeolite, silicate clay, etc. can be mentioned.

これらを単独又は混合して用いる。These can be used alone or in combination.

無機フィラーの平均粒径としては1μ〜10μのものが
好ましく、1μ〜5μのものが更に好ましい。粒径が1
0μを超えると気孔の緻密性や押出ラミネート加工性が
悪くなり、1部未満の粒径では有孔化が起こりにくい場
合がある。又、無機フィラーは脂肪酸又はその金属塩で
処理されたものがラミネート加工性9分散性の点から好
ましい。
The average particle size of the inorganic filler is preferably 1 μ to 10 μ, more preferably 1 μ to 5 μ. Particle size is 1
When the particle size exceeds 0μ, the density of pores and extrusion lamination processability deteriorate, and when the particle size is less than 1 part, it may be difficult to form pores. Further, it is preferable that the inorganic filler is treated with a fatty acid or a metal salt thereof from the viewpoint of laminating processability and dispersibility.

熱可塑性樹脂及び無機フィラーに配合する液状成分とし
ては250℃以上の耐熱性を持つ可塑剤又は液状炭化水
素ポリマーを一種又は、それ以上用いれば良い。押出し
ラミネート加工の際液状成分の耐熱性が悪いと発泡し成
膜が不可能となる。
As the liquid component to be mixed with the thermoplastic resin and inorganic filler, one or more plasticizers or liquid hydrocarbon polymers having heat resistance of 250° C. or higher may be used. During extrusion lamination, if the heat resistance of the liquid component is poor, it will foam and become impossible to form a film.

従って液状成分の耐熱性が良好、すなわち加熱減量が小
さいことが重要である。熱天秤で測定した(昇温度5℃
/min、空気中)加熱減量が250℃において5%更
に好ましくは326以下が好ましい。このような成分と
してはエポキシ化大豆曲、液状ポリブテンが最も好適で
ある。
Therefore, it is important that the liquid component has good heat resistance, that is, the loss on heating is small. Measured with a thermobalance (temperature increase: 5℃)
/min, in air) heating loss is 5% at 250° C., more preferably 326 or less. As such components, epoxidized soybean powder and liquid polybutene are most suitable.

多孔性基材としてはポリエステル、高密度ポリエチレン
、プロピレン−エチレン共重合体、レーヨン、ナイロン
等の合成繊維及び天然繊維からなる、不織布、織布およ
び混抄不織布、薄葉紙等の表面状態の粗な紙、さらにガ
ラス繊維、ロックウール等からなる無機系の不織布状基
材を挙げることができる。これら多孔性基材としては空
隙率が95%以下のものが好ましく、90%以下が更に
好ましい。なぜなら、押出ラミネート加工において、圧
着により多孔性基材の空隙率は一時的に低下するが圧着
後見の空隙率近くまで回復する。その際空隙率が95%
を越えるものは熱可塑性樹脂フィルムと多孔性基材との
接着点がはがれ、破けが生じ易い為である。
Porous substrates include nonwoven fabrics, woven fabrics, and mixed nonwoven fabrics made of synthetic fibers and natural fibers such as polyester, high-density polyethylene, propylene-ethylene copolymers, rayon, and nylon, and papers with rough surfaces such as thin paper. Further examples include inorganic nonwoven fabric base materials such as glass fiber and rock wool. These porous substrates preferably have a porosity of 95% or less, more preferably 90% or less. This is because, in extrusion lamination, the porosity of the porous base material temporarily decreases due to pressure bonding, but after the pressure bonding, the porosity returns to close to that of the porosity of the porous base material. At that time, the porosity is 95%
This is because the bonding point between the thermoplastic resin film and the porous base material is likely to peel off and tear if it exceeds this range.

熱可塑性樹脂、無機フィラー及び液状成分の配合割合は
熱可塑性樹脂100重量部に対して無機フィラーは20
〜300部が好ましく100〜200部が更に好ましい
。無機フィラーが20部に満たないと有孔化ポイントが
極端に少なくなったり、また300部を越えると混線性
分散性、押出ラミネートのドローダウン性が劣り満足す
る通気性複合シートは得られない場合がある。液状成分
の配合割合は熱可塑性樹脂100重量部に対して2〜5
0部である。2部に満たないと有孔化が起こりにくくな
ったり、50部を超えると押出ラミネートの成形性が悪
くなり極端な場合サージング等の問題が生じる場合があ
る。
The blending ratio of thermoplastic resin, inorganic filler, and liquid component is 20 parts by weight of inorganic filler per 100 parts by weight of thermoplastic resin.
-300 parts are preferable, and 100-200 parts are more preferable. If the amount of inorganic filler is less than 20 parts, the perforation point will be extremely small, and if it exceeds 300 parts, crosstalk dispersion and drawdown properties of extrusion laminate will be poor, making it impossible to obtain a satisfactory breathable composite sheet. There is. The blending ratio of the liquid component is 2 to 5 parts by weight per 100 parts by weight of the thermoplastic resin.
It is 0 copies. If the amount is less than 2 parts, it becomes difficult to form pores, and if it exceeds 50 parts, the moldability of the extrusion laminate will deteriorate, and in extreme cases, problems such as surging may occur.

混合はヘンシェルミキサー、ダンブラー型混合機等の混
合機が適宜選ばれる。混合順序としては例えば熱可塑性
樹脂パウダーに液状成分を加え充分混合し、種類によっ
ては予備乾燥し水分を除去した無機フィラーを次に加え
再度混合し配合物を得る。これらの配合物は通常の一軸
スクリユー押出機、又は二軸スクリュー押出機、ミキシ
ングロール、バンバリーミキサ−等の装置で混線、造粒
化される。
For mixing, a mixer such as a Henschel mixer or a dumbler type mixer is appropriately selected. As for the mixing order, for example, a liquid component is added to a thermoplastic resin powder and thoroughly mixed, and depending on the type, an inorganic filler that has been predried and water removed is then added and mixed again to obtain a blend. These blends are mixed and granulated using a conventional single-screw extruder, twin-screw extruder, mixing roll, Banbury mixer, or other equipment.

押出ラミネート成形は通常の押出、ラミネート装置で行
えば良い。すなわち多孔性基材を原反として必要に応じ
てコロナ放電処理、オゾン処理等の前処理を行い混合、
混練、造粒化された配合物を押出しラミネートする。樹
脂温度は使用される熱可塑性樹脂により適宜適正温度に
設定され例えばポリオレフィン系樹脂の場合、250〜
350℃か一般的である。しかしながら多孔性基材との
接若性が損なわない範囲でできるだけ低温の方が有孔化
ポイントが多くなるので好ましい。ラミネート厚みは1
0μ〜50μが好ましく、さらに好ましくは15〜30
μである。10μ未満では溶畿熱可塑性樹脂フィルム切
れが生ずる等加工性が悪く又50μを越えると有孔化ポ
イントが極端に少なくなる場合がある。
Extrusion lamination may be carried out using a conventional extrusion and lamination device. That is, the porous base material is used as a raw material, and if necessary, it is pretreated such as corona discharge treatment and ozone treatment, and then mixed.
The kneaded and granulated mixture is extruded and laminated. The resin temperature is set to an appropriate temperature depending on the thermoplastic resin used. For example, in the case of polyolefin resin, the temperature is 250 to
350°C is common. However, it is preferable to keep the temperature as low as possible without impairing the adhesive properties with the porous base material, since this increases the number of pore-forming points. Laminate thickness is 1
0μ to 50μ is preferable, more preferably 15 to 30μ
μ. If it is less than 10μ, the processability is poor, such as breakage of the melted thermoplastic resin film, and if it exceeds 50μ, the number of perforation points may be extremely reduced.

押出ラミネート成形においては圧着と冷却がほぼ同時に
行われる。冷却過程で熱可塑性樹脂フィルムに収縮力が
生じ無機フィラーと熱可塑性樹脂との境界面にボイドが
生じ熱可塑性フィルムが有孔化する。しかしキャストフ
ィルムとして成形した単体フィルムでは有孔化は起ζら
ない。
In extrusion lamination, pressing and cooling are performed almost simultaneously. During the cooling process, shrinkage force is generated in the thermoplastic resin film, creating voids at the interface between the inorganic filler and the thermoplastic resin, and the thermoplastic film becomes porous. However, porosity does not occur in a single film formed as a cast film.

また熱可塑性樹脂と無機フィラーのみの配合物を不織布
等の多孔性基材に押出ラミネーターシても有孔化は起こ
らない。
Further, even when a mixture of only a thermoplastic resin and an inorganic filler is extruded and laminated onto a porous substrate such as a nonwoven fabric, no porosity occurs.

[実施例] 実施例1 メルトインデックス(Ml)8.密度が0.917 g
/cm’である低密度ポリエチレン樹脂(東ソー株式会
社製[ペトロセン4203)のパウダー4 kgにエポ
キシ化大豆油(アデカ・アーガス化学株式会社製商品名
rD−130P41kgを添加しヘンシェルミキサーで
混合しさらに平均粒径2.2μの炭酸カルシウム(丸尾
カルシウム株式会社製「スノーライト5SJ)を6 k
g加え充分混合した組成物を50mmφのベント付−軸
スクリユー押出機(田辺プラスチック機械株式会社。
[Example] Example 1 Melt index (Ml)8. Density is 0.917 g
41 kg of epoxidized soybean oil (trade name: rD-130P, manufactured by Adeka Argus Chemical Co., Ltd.) was added to 4 kg of powder of low-density polyethylene resin (manufactured by Tosoh Corporation [Petrosen 4203]) with a particle size of 1.5 cm, mixed with a Henschel mixer, and then averaged. Calcium carbonate with a particle size of 2.2μ (“Snowlight 5SJ” manufactured by Maruo Calcium Co., Ltd.) was added to the
g and thoroughly mixed the composition using a 50 mmφ vented screw extruder (Tanabe Plastic Machinery Co., Ltd.).

型式US50)で混練造粒した。次いで25關φ押出機
を持つラミネーター(株式会社ブラコー製型式TP−3
50)を使用し材質がポリエステルで坪m 40 g 
/ rd 、空隙率75%の不織布(ユニチカ株式会社
製、TO403WDO)を原反とし押出ラミネート加工
した。
The mixture was kneaded and granulated using a model US50. Next, a laminator (Model TP-3 manufactured by Braco Co., Ltd.) with a 25 mm diameter extruder was used.
50), the material is polyester, and the weight is 40 g.
/rd, a nonwoven fabric with a porosity of 75% (manufactured by Unitika Co., Ltd., TO403WDO) was used as the raw fabric and extrusion laminated.

主な加工条件は樹脂温度300℃、引取温度60 m 
/ rn i n 、ラミネート厚み20μである。
The main processing conditions are resin temperature 300℃, take-up temperature 60m
/ r n i n , and the laminate thickness is 20 μm.

かくして得られた複合通気性シートの透湿度(JIs、
  20208.温度40℃、湿度90%)、耐水度(
J l5L−1069A法)を測定した結果を第1表に
記す。
The moisture permeability (JIs,
20208. temperature 40℃, humidity 90%), water resistance (
Table 1 shows the results of the measurements (J15L-1069A method).

実施例2 第3成分が液状ポリブテン(日本石油化学株式会社、H
V300)である他はすべて実施例1と同様に行ってシ
ートを得た。このシートの透湿度及び耐水度を測定した
結果を第1表に示す。
Example 2 The third component was liquid polybutene (Japan Petrochemical Co., Ltd., H
A sheet was obtained in the same manner as in Example 1 except for using V300). Table 1 shows the results of measuring the moisture permeability and water resistance of this sheet.

比較例1 実施例1と同じ条件で得られた組成物を50 wφのベ
ント付−軸スクリユー押出機(田辺プラスチックス株式
会社、型式VS50)で混線、造粒し次いで25o+m
φ押出機を持つラミネーター(株式会社プラコー製、型
式TP−350)を使用し多孔性基材と複合化せずキス
ストフィルムとして成形した。
Comparative Example 1 A composition obtained under the same conditions as Example 1 was mixed and granulated using a 50 wφ vented screw extruder (Tanabe Plastics Co., Ltd., model VS50), and then granulated at 25 o+m
Using a laminator (manufactured by Plako Co., Ltd., model TP-350) equipped with a φ extruder, it was molded as a KIST film without being composited with a porous substrate.

主な加1−条件は樹脂温度300℃、引取速度60m/
min、 ラミネート厚み20μである。このフィルム
に関し測定した透湿度、耐水度の結果を第1表に示す。
The main conditions are resin temperature 300℃, take-up speed 60m/
min, laminate thickness is 20μ. Table 1 shows the results of moisture permeability and water resistance measured for this film.

比較例2 25mmφ押出機の持つラミネーター(株式会社プラコ
ー製、型式TP−350)を使用し材質がポリエステル
で坪Q40g/d、空隙率75%の不織布(ユニチカ株
式会社製、TO403DO)を原反としメルトインデッ
クス(Ml)8、密度が0.917g/m″である低密
度ポリエチレン樹脂(東ソー株式会社製商品名「ベトロ
セン」?03)のパウダー4 kgに、平均粒径2.2
μの炭酸カルシウム(丸尾カルシウム株式会社製「スノ
ーライト5SJ)を6 kg添加し、充分混合した組成
4勿を50 mmφベルト付−軸スクリユー押出機(0
1辺プラスチック株式会社、型式VS50)で混練、造
粒し押出ラミネートした。主な加工条件は樹脂温度30
0℃、引取速度60m/min。
Comparative Example 2 Using a laminator (manufactured by Placo Co., Ltd., model TP-350) with a 25 mmφ extruder, a nonwoven fabric (manufactured by Unitika Co., Ltd., TO403DO) made of polyester, having a tsubo Q of 40 g/d, and a porosity of 75% was used as a raw material. To 4 kg of powder of low-density polyethylene resin (trade name "Betrocene" -03 manufactured by Tosoh Corporation) having a melt index (Ml) of 8 and a density of 0.917 g/m'', an average particle size of 2.2 was added.
6 kg of μ calcium carbonate (“Snowlight 5SJ” manufactured by Maruo Calcium Co., Ltd.) was added and thoroughly mixed.
The mixture was kneaded, granulated, and extrusion laminated using Ichibe Plastic Co., Ltd. (model VS50). The main processing conditions are resin temperature 30
0°C, take-up speed 60 m/min.

ラミネート厚み20μこのフィルムに関し測定した透湿
度、耐水度の結果を第1表に示す。
Laminate thickness: 20μ The results of moisture permeability and water resistance measured for this film are shown in Table 1.

[発明の効果] 本発明によれば多孔性基材と熱可塑性樹脂フィルムとの
接合と有孔化を同時に行うことが可能となった。その為
透湿度、耐水度に優れた通気性複合シートの製造速度の
高速化が可能となり、又、品質管理、工程管理が容品と
なった。
[Effects of the Invention] According to the present invention, it has become possible to bond a porous base material and a thermoplastic resin film and to form pores at the same time. As a result, it has become possible to increase the production speed of breathable composite sheets with excellent moisture permeability and water resistance, and quality control and process control have become easier.

また従来行われている溶剤系接着剤、ホットメルト接眉
剤による接若方法に比べ耐熱、耐溶剤性において優位に
ありその工業的価値は高い。
Furthermore, it has superior heat resistance and solvent resistance compared to conventional methods of applying eyebrows using solvent-based adhesives or hot-melt eyelids, and its industrial value is high.

Claims (1)

【特許請求の範囲】[Claims] (1)熱可塑性樹脂、無機フィラー及び250℃以上の
耐熱性をもつ液状成分からなる組成物を多孔性基材に押
出ラミネートすることを特徴とする通気性複合シートの
製造方法。
(1) A method for producing a breathable composite sheet, which comprises extrusion laminating a composition comprising a thermoplastic resin, an inorganic filler, and a liquid component having heat resistance of 250° C. or higher onto a porous base material.
JP63316293A 1988-12-16 1988-12-16 Manufacture of air-permeable composite sheet Pending JPH02162008A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63316293A JPH02162008A (en) 1988-12-16 1988-12-16 Manufacture of air-permeable composite sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63316293A JPH02162008A (en) 1988-12-16 1988-12-16 Manufacture of air-permeable composite sheet

Publications (1)

Publication Number Publication Date
JPH02162008A true JPH02162008A (en) 1990-06-21

Family

ID=18075500

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63316293A Pending JPH02162008A (en) 1988-12-16 1988-12-16 Manufacture of air-permeable composite sheet

Country Status (1)

Country Link
JP (1) JPH02162008A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998058799A1 (en) * 1997-06-25 1998-12-30 Kimberly-Clark Worldwide, Inc. Low gauge films and film/nonwoven laminates
US6797377B1 (en) * 1998-06-30 2004-09-28 Kimberly-Clark Worldwide, Inc. Cloth-like nonwoven webs made from thermoplastic polymers

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998058799A1 (en) * 1997-06-25 1998-12-30 Kimberly-Clark Worldwide, Inc. Low gauge films and film/nonwoven laminates
US6797377B1 (en) * 1998-06-30 2004-09-28 Kimberly-Clark Worldwide, Inc. Cloth-like nonwoven webs made from thermoplastic polymers

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