JPH0314059B2 - - Google Patents
Info
- Publication number
- JPH0314059B2 JPH0314059B2 JP58113484A JP11348483A JPH0314059B2 JP H0314059 B2 JPH0314059 B2 JP H0314059B2 JP 58113484 A JP58113484 A JP 58113484A JP 11348483 A JP11348483 A JP 11348483A JP H0314059 B2 JPH0314059 B2 JP H0314059B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- stretching
- tubular
- mandrel
- stretched
- 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 - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/28—Shaping by stretching, e.g. drawing through a die; Apparatus therefor of blown tubular films, e.g. by inflation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D7/00—Producing flat articles, e.g. films or sheets
- B29D7/01—Films or sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D99/00—Subject matter not provided for in other groups of this subclass
- B29D99/005—Producing membranes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/06—Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
- B29K2105/16—Fillers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/48—Wearing apparel
- B29L2031/4871—Underwear
- B29L2031/4878—Diapers, napkins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/755—Membranes, diaphragms
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
【発明の詳細な説明】
本発明は、ポリオレフイン系樹脂と無機充填剤
との組合物からなる未延伸フイルムを二軸延伸し
てなる、ソフト感を有する通気性フイルムの製造
方法に関する。
従来より、ポリオレフイン系樹脂と無機充填剤
との組成物からなる未延伸フイルムを二軸延伸し
て、フイルムに連通したボイドを発生させて通気
性フイルムを製造する方法は多数提案されてい
る。
この場合の二軸延伸方法としては、フラツト状
で二軸延伸する方法と、管状を保持した状態で二
軸延伸する方法とがある。
フラツト状で二軸延伸する方法は、横方向に延
伸する際にクリツプでフイルムを把持し延伸する
ために把持した部分が製品にならない点、この方
法に使用する延伸設備が非常に高価な点等より、
製品コストが高くなる欠点を有している。更に、
通常商業的に使用されている方法は、未延伸フイ
ルムを縦方向と横方向とに別々の工程で延伸する
ため、延伸されたフイルムの機械的特性がアンバ
ランスになる欠点を有している。
管状を保持した状態で二軸延伸する方法は、フ
ラツト状の前述の欠点を解決するために提案され
たもので、フラツト状で二軸延伸する方法に比較
し、設備費が少なく、クリツプを使用しないこと
から未延伸部分が残ることなく全て延伸されるた
め製品になる効率が高く、更に、縦方向と横方向
とがほぼ同時に延伸されるために機械的性質がバ
ランスしているという特徴を有している。
この二軸延伸法には、加圧気体の内圧により延
伸する内圧バブル延伸法と、管状未延伸フイルム
の内部に円錐台形のマンドレルを挿入して延伸す
るマンドレル延伸法とがある。
内圧バブル延伸法は、低速ロールと高速ロール
との周速度差により縦方向に延伸しながら、ロー
ル間で内圧により横方向(中周方向)に延伸する
方法であり、内圧気体の漏洩を防ぐために低速ロ
ールおよび高速ロールはニツプロール方式となつ
ている。従つて、ポリオレフイン系樹脂と無機充
填剤との組成物からなる管状未延伸フイルムをこ
の内圧バブル延伸法で二軸延伸しようとすると、
管状未延伸フイルムが低速ニツプロールを通過す
る際にニツプロールにより二つ折り状態に押圧さ
れるため、折り曲げられた両端耳部は塑性変形し
無機充填剤が樹脂より剥離する。この局部的に剥
離した部分は低い延伸応力で延伸が開始するため
に、延伸中の管状フイルムの形状が変化し延伸が
不安定になるとともに、この剥離部分は延伸倍率
が局部的に高くなるために、延伸後のフイルムに
ボイドむらが縦筋となつて発現し品質の均一な通
気性フイルムが得られない。更に、この内圧バブ
ル延伸法は、低速ロールと高速ロールとのロール
間に加圧気体を封じ込め横方向(円周方向)に延
伸する方法であるため、通気性フイルムにおいて
は、フイルムの内側から外側に向けて内部の加圧
気体が漏洩してしまい連続安定生産が困難であ
る。
一方、マンドレル延伸法は、内圧バブル延伸法
におけるような延伸不安定性及び縦筋を改良する
ために提案された方法であり、この延伸法におい
ては、円錐台形のマンドレルに沿わせながら延伸
するために、局部的な延伸による延伸の不安定性
が改良され、また、加圧気体を封じ込める必要が
ないのでニツプロールによる折目が発生しなくな
り、従つて縦筋による品質不良がなくなる。とこ
ろが、円錐台形のマンドレルに沿わせながら延伸
するために、延伸フイルムの厚み方向にかなりの
圧縮応力が作用し、延伸により発現したボイドが
つぶされ品質のよい通気性フイルムが得られない
という欠点を有している。
以上のように、ポリオレフイン系樹脂と無機充
填剤との組成物からなる未延伸フイルムと二軸延
伸して通気性フイルムを製造する従来の方法で
は、方向と横方向との機械的性質のバランスがと
れ、かつ通気性の優れたフイルムを均一な厚みで
安定して製造するには到つていないのが現状であ
る。
他方、この通気性フイルムは、紙おむつ、ある
いは生理用品等の衛生用品等用途への応用が試み
られ始めており、この場合、シヤリシヤリした紙
様でなく、ソフト感を有する布様の通気性フイル
ムが要求される。
本発明は、上述の現状に鑑み、従来の製造方法
における問題点および要望を解決することを目的
としてなされたもので、以下詳述すれば、本発明
の通気性フイルムの製造方法は、密度が0.910〜
0.940g/cm3、メルトフローレートが0.1〜5g/
10分、数平均分子量に対する重量平均分子量の比
で表されるQ値が4以上であるエチレン−α−オ
レフイン共重合体42〜87体積%と無機充填剤58〜
13体積%との組成物からなる管状未延伸フイルム
を円錐台形のマンドレルに沿わせながら二軸延伸
し、引き続き、管状二軸延伸フイルムの外側から
気体を吹付けることにより該フイルムを冷却する
と共に、該フイルムの内側から連続的に気体を吹
込むことにより該フイルムの外側に貫通させるこ
とを特徴とする。
ここで、エチレン−α−オレフイン共重合体と
は、C3〜C8の分子骨格であるα−オレフインが
1〜20重量%、好ましくは3〜15重量%、エチレ
ンが99〜80重量%、好ましくは97〜85重量%から
なる直鎖状低密度エチレン共重合体であり、遷移
金属化合物と有機金属化合物とを組合せた触媒を
用いてイオン反応によりエチレンとC3〜C8の分
子骨格であるα−オレフインを1つ以上含んで共
重合させて生成される樹脂であり、その密度が
0.910〜0.940g/cm3、好ましくは0.916〜0.935
g/cm3、メルトフローレート(MFR)が0.1〜5
g/10分、好ましくは0.1〜3g/10分、数平均
分子量に対する重量平均分子量の比で表されるQ
値が4以上、好ましくは6以上の範囲に含まれる
ものであつて、一般的に知られている酸素ラジカ
ルを開始剤とし高圧力下でラジカル反応によりエ
チレンを重合させて生成される分岐状低密度ポリ
エチレン樹脂とは、分子構造、溶融特性、結晶化
特性、固体物性、延伸特性において異なつた性能
を有するものである。異なるインデツクスを有す
るエチレン−α−オレフイン共重合体の混合物で
あつても、混合物の密度、MFR、Q値が前述の
限定範囲内であれば、本発明に使用してもよい。
好ましくは単一の共重合体である。
この共重合体の密度が0.910g/cm3未満になる
と均一延伸性が悪化し、0.940g/cm3を越えると
延伸フイルムのソフト感が損われる。また、
MFRが0.1g/10分未満になると未延伸フイルム
をダイ間隙より溶融押出しする際異常流動が発生
し均一な未延伸フイルムが得られなくなり、5
g/10分を越えると均一延伸性が悪化する。ま
た、Q値が4未満になると均一延伸性が悪化し厚
みの均一性が損われる。
また、無機充填剤は、炭酸カルシウム、酸化カ
ルシウム、タルク、クレー、シリカ、酸化チタ
ン、アルミナ、硫酸アルミニウム等であり、単独
あるいは混合状態で用いることができる。好まし
い無機充填剤の形態としては、板状、棒状、針状
以外の球状、粒状、不定形等であり、その平均粒
径は0.1〜5μ、好ましくは0.6〜3μである。平均粒
径が0.1μ未満になると未延伸フイルムの延伸時の
伸びがなくなつて二軸延伸が困難になり、5μを
越えると二軸延伸フイルムの表面の凹凸が荒くな
り通気性フイルムとして望ましくなるとともに、
60μ以下の薄いフイルムを製造するにおいて連続
安定延伸性が損われる。
エチレン−α−オレフイン共重合体と無機充填
剤との混練方法としては、一軸あるいは二軸押出
機、バンバリーミキサー、ニーダー、ミキシング
ロール等による加熱混練が採用できる。加熱混練
の際には、分散剤、熱安定剤、紫外線吸収剤、滑
剤、顔料、帯電防止剤等通常添加する添加剤を同
時に混練できる。特に、分散剤として、炭素数12
以上の高級脂肪酸が好結果を与える。無機充填剤
は、加熱混練する前にこれらの分散剤等で処理さ
れていてもよい。
エチレン−α−オレフイン共重合体と無機充填
剤との組成比は、エチレン−α−オレフイン共重
合体が42〜87体積%、好ましくは55〜80体積%、
無機充填剤が58〜13体積%、好ましくは45〜20体
積%である。無機充填剤が13体積%未満になる
と、エチレン−α−オレフイン共重合体と無機充
填剤との界面が剥離してできる隣接したボイドど
うしが連通しなくなり、通気性が得られなくな
る。また、58体積%を越えると、未延伸フイルム
の延伸時の伸びがなくなり二軸延伸が困難にな
る。
本発明にいう円錐台形のマンドレルに沿わせな
がら二軸延伸するマンドレル延伸法とは、管状未
延伸フイルムの中に、一端が管状未延伸フイルム
の直径に等しいかあるいは若干小さい直径を有
し、他端が延伸しようとする横方向(円周方向)
の延伸倍率にほぼ等しい直径を有する円錐台形の
マンドレルを挿入し、該マンドレルの傾斜した側
面に管状未延伸フイルムを沿わせながら、マンド
レルの後方に位置する引き取りニツプロールによ
つて延伸後冷却された延伸フイルムが引き取られ
る際に発生する力により、実質的に円錐台形のマ
ンドレル上で面圧を受けた状態で横方向(円周方
向)と縦方向とに延伸する方法をいう。このマン
ドレルの支持方法としては、管状未延伸フイルム
を押し出す環状のダイに連結した支持棒に、マン
ドレルの小なる径の端面を固定する方法が好まし
い。
この延伸における延伸温度は、いわゆる延伸に
より配向が起こる温度であつて、公知の如く通常
は比較的広い範囲の温度幅を有し、フイルム加工
業界に於いては容易に確定可能である。一般に融
点よりわずかに低い温度範囲にあるが、マンドレ
ル延伸の場合には、マンドレルに接触させて延伸
するので、融点をTm(℃)、延伸温度をTs(℃)
とすると、Tm−50≦Ts≦Tm−5(℃)が適す
る。延伸温度への加熱は、マンドレル等を介して
内部より加熱してもよいし、外部より加熱しても
よいが、均一加熱の面より少なくとも内部は加熱
することが好ましい。
また、延伸倍率は、縦横それぞれ1.5〜4倍が
安定延伸に適する。
本発明においては、マンドレルを離れ実質的に
延伸を終了した管状二軸延伸フイルムを、該フイ
ルムの外側から気体、一般には空気を吹付ける公
知の方法で冷却すると共に、該フイルムの内側か
ら連続的に気体を吹込むことにより該フイルムの
外側に気体を貫通させる。
この際の気体の吹込み量は、得られた管状二軸
延伸フイルムの物性および形状、延伸速度、冷却
気体の温度および吹付け量等により変化するため
一義的には決定し得ないが、20℃で0.1〜150Nl/
m2・分、好ましくは1〜70Nl/m2・分の範囲で、
管状二軸延伸フイルムが延伸終了時とほゞ同等の
口径を保つように適宜設定される。冷却気体の吹
付け量を多くしながら、この気体の吹込み量を多
くすると、通気度が漸次大きな通気性フイルムが
得られる。また、この気体としては空気が最も一
般的である。なお、この気体吹込みのためには、
外部の加圧源に連結し、環状ダイ、および前述の
マンドレル支持棒、マンドレルを貫通してマンド
レルの大なる径の端面に開口した導管を設けてお
く。
本発明における通気性フイルムの製造工程は次
の5つの工程よりなる。即ち、管状未延伸フイル
ムを環状ダイのダイリツプ間隙より溶融状態で押
し出し、ダイリツプ径と等しいかあるいはこれよ
り大きい径となした後、冷却固化し連続的に引き
取る管状未延伸フイルム製造工程と、同フイルム
を適正延伸温度に加熱する予熱工程と、同加熱さ
れた管状未延伸フイルムを円錐台形のマンドレル
の表面に面圧を受けた状態で沿わせながら二軸延
伸する延伸工程と、マンドレルを離れ実質的に延
伸を終了した管状状態にあるフイルムを、管状フ
イルムの外側より制御された冷却気体により冷却
するとともに、管状状態にあるフイルムの内側か
ら外側に向けて、制御された加圧気体を連続的に
管状フイルム円周全域に渡り貫通させて延伸フイ
ルムに通気性を付与する工程と、延伸されたフイ
ルムを冷却した後製品として巻きとる巻き取り工
程とよりなる。
本発明によつて製造される通気性フイルムの物
性は、エチレン−α−オレフイン共重合体の物
性、無機充填剤の粒径、種類、充填割合、二軸延
伸条件である延伸温度、縦横方向の延伸倍率、冷
却気体の吹付け量、内側からの気体の吹込み量等
により自由にコントロール可能である。通気性フ
イルムの厚みが25〜150μの場合、JIS P8117で測
定した通気度は25〜30000秒/100c.c.、JIS Z
0203で測定した透湿度は300〜25000g/m2・24時
間の範囲の値を有するのが望ましく、特に厚みは
ソフト感等より60μ以下が好ましい。
以下に本発明の実施例を比較例とともに示し具
体的に説明する。尚、本発明は実施例により限定
されるものではない。
実施例 1
エチレン−ブテン−1重量合体(密度0.923
g/cm3、MFR0.9g/10分、Q値11、融点121℃)
のパウダー65体積%、重質炭酸カルシウム(平均
粒径1.2μ、板状棒状でない不定形)35体積、エチ
レン−ブテン−1共重合体100重量部に対して熱
安定剤(2,6−ジ−t−ブチル−p−クレゾー
ル)0.1重量部、重質炭酸カルシウム100重量部に
対して分散剤(オレイン酸)1.0重量部等をスー
パーミキサーで5分間混合した後、二軸押出機よ
り200℃でストランド状に押出した後、ペレツト
状に切断した。
得られたペレツトを、スクリユー径50φ、L/
D25の押出機に取り付けた環状ダイ(リツプ径
75φ、リツプ間隙1mmの4条スパイラルダイ)よ
り210℃で押出した後、内部を5℃の水が循環す
る直径100φの冷却マンドレルに接触せしめ、ブ
ロー比1.33で冷却固化して厚み130μの管状未延伸
フイルムを4m/分で引き取つた。
このフイルムを、冷却マンドレルの下方に連結
された直径98φの予熱マンドレルで110℃に加熱
した後、予熱マンドレルに直結する端面の直径が
98φでもう一方の端面の直径が250φで、その円錐
角が90゜の表面を凹凸0.5μに梨地加工した110℃の
円錐台形のマンドレル表面に沿わせながら横方向
(円周方向)に2.5倍延伸しながら縦方向に3.0倍
延伸し、引き続き、マンドレルを離れた管状状態
にある二軸延伸フイルムの外側全周に、マンドレ
ルの下端から50mmの位置にて、直径350φ、リツ
プ間隙3mmのエアーリングより、15℃、10m/秒
の空気を吹き付けるとともに、マンドレルの下端
の導管より、管状フイルムの内部に20℃の空気を
40Nl/m2・分の割合で連続的に吹込むことによ
り、内側より外側に向けて連続的にフイルムの厚
み方向に貫通させながら、ニツプロールにより引
き取ることにより管状二軸延伸通気性フイルムを
得た。
得られた通気性フイルムの外観および物性を表
1に示す。なお透湿度はJIS Z0208、通気度は
JIS P8117、引裂強度はJIS Z1702にそれぞれ基
づいて測定した。
実施例 2
実施例1において、エチレン−ブテン−1共重
合体の代わりに、エチレン−プロピレン−ブテン
−1共重合体(密度0.918g/cm3、MFR0.701g/
10分、Q値6、融点123℃)のパウダーを用い、
管状二軸延伸フイルムの冷却空気の吹付けを5
m/秒とし、空気の吹込みを20Nl/m2・分とし
た以外、実施例1と同様な方法により通気性フイ
ルムを得た。得られた通気性フイルムの結果を表
1に合せて記す。
比較例 1
実施例1において、密度0.920g/cm3、MFR1.0
g/10分、Q値3.4、融点124℃のエチレン−ブテ
ン−1共重合体を用い、予熱温度と延伸温度を
113℃とした以外、実施例1と同一条件で延伸し、
通気性フイルムを製造した。結果を表1に合せて
記す。
比較例 2
実施例1において、エチレン−ブテン−1共重
合体の代わりに高密度ポリエチレン(密度0.950
g/cm3、MFR0.05g/10分、融点132℃)のパウ
ダーを用い、290℃でペレツト化し、260℃で管状
未延伸フイルムとして押出し、予熱温度及び延伸
温度を118℃に条件変更した以外、実施例1と同
一条件で延伸し、通気性フイルムを得た。結果を
表1に合せて記す。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a breathable film having a soft feel, which is obtained by biaxially stretching an unstretched film made of a combination of a polyolefin resin and an inorganic filler. Conventionally, many methods have been proposed for producing a breathable film by biaxially stretching an unstretched film made of a composition of a polyolefin resin and an inorganic filler to generate voids communicating with the film. Biaxial stretching methods in this case include a method of biaxial stretching in a flat state and a method of biaxial stretching while maintaining a tubular shape. The method of biaxial stretching in a flat form has the disadvantages that the film is gripped with a clip and stretched in the horizontal direction, so the gripped part does not become a product, and the stretching equipment used in this method is very expensive. Than,
The disadvantage is that the product cost is high. Furthermore,
The methods commonly used commercially have the disadvantage that the unstretched film is stretched in separate steps in the machine direction and in the transverse direction, resulting in unbalanced mechanical properties of the stretched film. The method of biaxial stretching while maintaining the tubular shape was proposed to solve the above-mentioned drawbacks of the flat shape.Compared to the method of biaxial stretching with the flat shape, the equipment cost is lower and it uses clips. Since it is not stretched at all, it is fully stretched without leaving any unstretched parts, resulting in high efficiency in turning it into a product.Furthermore, because it is stretched almost simultaneously in the longitudinal and transverse directions, its mechanical properties are well-balanced. are doing. This biaxial stretching method includes an internal pressure bubble stretching method in which the film is stretched using the internal pressure of pressurized gas, and a mandrel stretching method in which a truncated conical mandrel is inserted into the interior of a tubular unstretched film for stretching. The internal pressure bubble stretching method is a method of stretching in the longitudinal direction due to the difference in circumferential speed between low-speed rolls and high-speed rolls, while stretching in the horizontal direction (middle circumferential direction) using internal pressure between the rolls.In order to prevent leakage of internal pressure gas, The low-speed roll and high-speed roll are of the nip roll type. Therefore, when attempting to biaxially stretch a tubular unstretched film made of a composition of a polyolefin resin and an inorganic filler using this internal pressure bubble stretching method,
When the tubular unstretched film passes through the low-speed nip rolls, it is pressed into a two-fold state by the nip rolls, so the bent edges at both ends are plastically deformed and the inorganic filler is peeled off from the resin. Since stretching starts at a low stretching stress in this locally peeled part, the shape of the tubular film during stretching changes and the stretching becomes unstable, and the stretching ratio locally increases in this peeled part. Moreover, void unevenness appears as vertical streaks in the stretched film, making it impossible to obtain a breathable film of uniform quality. Furthermore, this internal pressure bubble stretching method is a method in which pressurized gas is confined between low-speed rolls and high-speed rolls and stretched in the transverse direction (circumferential direction). The internal pressurized gas leaks, making continuous and stable production difficult. On the other hand, the mandrel stretching method is a method proposed to improve stretching instability and longitudinal streaks as in the internal pressure bubble stretching method. Stretching instability caused by local stretching is improved, and since there is no need to confine pressurized gas, creases due to nip rolls do not occur, and quality defects due to longitudinal stripes are eliminated. However, since the stretched film is stretched along a truncated conical mandrel, considerable compressive stress acts on the stretched film in the thickness direction, and the voids developed by stretching are crushed, making it impossible to obtain a high-quality breathable film. have. As described above, in the conventional method of manufacturing a breathable film by biaxially stretching an unstretched film made of a composition of a polyolefin resin and an inorganic filler, the balance of mechanical properties in the direction and the transverse direction is not achieved. At present, it has not yet been possible to stably produce a film with a uniform thickness that is easy to remove and has excellent air permeability. On the other hand, attempts are being made to apply this breathable film to sanitary products such as disposable diapers and sanitary products, and in this case, a breathable film that has a soft cloth-like feel is required instead of a paper-like paper-like feel. be done. In view of the above-mentioned current situation, the present invention was made with the aim of solving the problems and demands of conventional manufacturing methods. 0.910〜
0.940g/cm 3 , melt flow rate 0.1~5g/
10 minutes, 42 to 87% by volume of an ethylene-α-olefin copolymer with a Q value expressed as the ratio of weight average molecular weight to number average molecular weight of 4 or more and 58 to 87% by volume of an inorganic filler.
A tubular unstretched film made of a composition of 13% by volume is biaxially stretched along a truncated conical mandrel, and then the film is cooled by blowing gas from the outside of the tubular biaxially stretched film. It is characterized in that gas is continuously blown from the inside of the film to penetrate the outside of the film. Here, the ethylene-α-olefin copolymer is 1 to 20% by weight, preferably 3 to 15% by weight of α-olefin, which is a C 3 to C 8 molecular skeleton, and 99 to 80% by weight of ethylene. Preferably, it is a linear low-density ethylene copolymer consisting of 97 to 85% by weight, which is formed by an ionic reaction between ethylene and a C 3 to C 8 molecular skeleton using a catalyst that combines a transition metal compound and an organometallic compound. It is a resin produced by copolymerizing one or more α-olefins, and its density is
0.910-0.940g/ cm3 , preferably 0.916-0.935
g/cm 3 , melt flow rate (MFR) 0.1-5
g/10 min, preferably 0.1 to 3 g/10 min, Q expressed as the ratio of weight average molecular weight to number average molecular weight
A branched low-carbon compound whose value is in the range of 4 or more, preferably 6 or more, and is produced by polymerizing ethylene through a radical reaction under high pressure using a commonly known oxygen radical as an initiator. Density polyethylene resins have different performance in molecular structure, melting properties, crystallization properties, solid physical properties, and stretching properties. A mixture of ethylene-α-olefin copolymers having different indexes may be used in the present invention as long as the density, MFR, and Q value of the mixture are within the aforementioned limited ranges.
Preferably it is a single copolymer. When the density of this copolymer is less than 0.910 g/cm 3 , uniform stretchability deteriorates, and when it exceeds 0.940 g/cm 3 , the soft feel of the stretched film is impaired. Also,
If the MFR is less than 0.1 g/10 minutes, abnormal flow will occur when the unstretched film is melt-extruded from the die gap, making it impossible to obtain a uniform unstretched film.
If it exceeds g/10 minutes, uniform stretchability will deteriorate. Furthermore, when the Q value is less than 4, uniform stretchability deteriorates and thickness uniformity is impaired. Inorganic fillers include calcium carbonate, calcium oxide, talc, clay, silica, titanium oxide, alumina, aluminum sulfate, etc., and can be used alone or in a mixed state. Preferred forms of the inorganic filler include plate-like, rod-like, spherical, granular, and amorphous shapes other than needle-like shapes, and the average particle size thereof is 0.1 to 5 μm, preferably 0.6 to 3 μm. When the average particle size is less than 0.1μ, the unstretched film loses its elongation during stretching, making biaxial stretching difficult; when it exceeds 5μ, the surface of the biaxially stretched film becomes rough, making it undesirable as a breathable film. With,
When producing thin films of 60μ or less, continuous stable stretchability is impaired. As a method for kneading the ethylene-α-olefin copolymer and the inorganic filler, heating kneading using a single-screw or twin-screw extruder, a Banbury mixer, a kneader, a mixing roll, etc. can be employed. During heating and kneading, commonly used additives such as dispersants, heat stabilizers, ultraviolet absorbers, lubricants, pigments, and antistatic agents can be kneaded at the same time. In particular, as a dispersant, carbon number 12
The above higher fatty acids give good results. The inorganic filler may be treated with these dispersants or the like before being heated and kneaded. The composition ratio of the ethylene-α-olefin copolymer and the inorganic filler is such that the ethylene-α-olefin copolymer is 42 to 87% by volume, preferably 55 to 80% by volume,
The amount of inorganic filler is 58-13% by volume, preferably 45-20% by volume. If the inorganic filler content is less than 13% by volume, adjacent voids formed by peeling of the interface between the ethylene-α-olefin copolymer and the inorganic filler will no longer communicate with each other, making it impossible to obtain air permeability. Moreover, if it exceeds 58 volume %, the unstretched film loses its elongation during stretching, making biaxial stretching difficult. The mandrel stretching method in which biaxial stretching is carried out along a truncated conical mandrel as used in the present invention refers to the method of biaxially stretching a tubular unstretched film along a truncated conical mandrel. Lateral direction (circumferential direction) in which the end is trying to stretch
A truncated conical mandrel having a diameter approximately equal to the stretching ratio is inserted, and while the tubular unstretched film is placed along the slanted side of the mandrel, it is stretched and cooled by a take-up roll located behind the mandrel. This is a method in which the film is stretched in the transverse direction (circumferential direction) and the longitudinal direction while being subjected to surface pressure on a substantially truncated conical mandrel due to the force generated when the film is taken off. As a method for supporting this mandrel, it is preferable to fix the end face of the mandrel with a small diameter to a support rod connected to an annular die for extruding the tubular unstretched film. The stretching temperature in this stretching is the temperature at which orientation occurs due to so-called stretching, and as is known, usually has a relatively wide temperature range and can be easily determined in the film processing industry. Generally, the temperature range is slightly lower than the melting point, but in the case of mandrel stretching, the stretching is done in contact with the mandrel, so the melting point is Tm (℃) and the stretching temperature is Ts (℃).
Then, Tm-50≦Ts≦Tm-5 (°C) is suitable. Heating to the stretching temperature may be done from the inside via a mandrel or the like, or from the outside, but it is preferable to heat at least the inside for uniform heating. Further, a stretching ratio of 1.5 to 4 times in both length and width is suitable for stable stretching. In the present invention, the tubular biaxially stretched film that has left the mandrel and has substantially finished stretching is cooled by a known method of blowing gas, generally air, from the outside of the film, and continuously from the inside of the film. By blowing gas into the film, the gas is passed through the outside of the film. The amount of gas blown at this time cannot be determined uniquely because it varies depending on the physical properties and shape of the obtained tubular biaxially stretched film, the stretching speed, the temperature of the cooling gas, the amount of blown gas, etc. 0.1~150Nl/℃
m 2 ·min, preferably in the range of 1 to 70Nl/m 2 ·min,
The diameter of the tubular biaxially stretched film is set as appropriate so that the diameter is approximately the same as that at the end of stretching. By increasing the amount of cooling gas blown and increasing the amount of this gas blown, a breathable film with gradually increasing air permeability can be obtained. Moreover, air is the most common gas. In addition, for this gas injection,
A conduit is provided that is connected to an external pressure source, passes through the annular die, the aforementioned mandrel support rod, and the mandrel, and opens at the large diameter end face of the mandrel. The manufacturing process of the breathable film in the present invention consists of the following five steps. That is, a process for manufacturing a tubular unstretched film in which a tubular unstretched film is extruded in a molten state through the die lip gap of an annular die, the diameter is equal to or larger than the die lip diameter, the film is cooled and solidified, and then continuously withdrawn; a preheating step in which the heated tubular unstretched film is heated to an appropriate stretching temperature; a stretching step in which the heated tubular unstretched film is biaxially stretched along the surface of a truncated conical mandrel under surface pressure; The film, which is in a tubular state after being stretched, is cooled by controlled cooling gas from the outside of the tubular film, and controlled pressurized gas is continuously applied from the inside of the tubular film to the outside. It consists of a step of penetrating the entire circumference of the tubular film to impart air permeability to the stretched film, and a winding step of cooling the stretched film and then winding it up as a product. The physical properties of the breathable film produced by the present invention include the physical properties of the ethylene-α-olefin copolymer, the particle size, type, and filling ratio of the inorganic filler, the stretching temperature (biaxial stretching conditions), and the longitudinal and lateral stretching conditions. It can be freely controlled by the stretching ratio, the amount of cooling gas blown, the amount of gas blown from the inside, etc. When the thickness of the breathable film is 25-150μ, the air permeability measured according to JIS P8117 is 25-30000 seconds/100c.c., JIS Z
The moisture permeability measured by 0203 is preferably in the range of 300 to 25,000 g/m 2 ·24 hours, and the thickness is preferably 60 μm or less in view of the soft feel. Examples of the present invention will be shown below together with comparative examples and will be specifically explained. Note that the present invention is not limited to the examples. Example 1 Ethylene-butene-1 weight combination (density 0.923
g/ cm3 , MFR0.9g/10min, Q value 11, melting point 121℃)
65% by volume of powder, 35% by volume of heavy calcium carbonate (average particle size 1.2μ, amorphous, not plate-like or rod-like), 100 parts by weight of ethylene-butene-1 copolymer, heat stabilizer (2,6-di -0.1 part by weight of (t-butyl-p-cresol) and 1.0 part by weight of a dispersant (oleic acid) with 100 parts by weight of heavy calcium carbonate were mixed in a super mixer for 5 minutes, and then heated to 200°C using a twin-screw extruder. After extruding it into a strand, it was cut into pellets. The obtained pellets were passed through a screw with a screw diameter of 50φ, L/
An annular die (lip diameter) attached to a D25 extruder
After extruding at 210℃ through a 75φ, 4-row spiral die with a lip gap of 1mm, it is brought into contact with a 100φ diameter cooling mandrel in which water at 5℃ circulates, and is cooled and solidified at a blow ratio of 1.33 to form a tubular blank with a thickness of 130μ. The stretched film was taken off at a rate of 4 m/min. After heating this film to 110℃ with a preheating mandrel with a diameter of 98φ connected below the cooling mandrel, the diameter of the end face directly connected to the preheating mandrel is
The diameter of the other end face is 98φ and the diameter of the other end is 250φ, and the surface with a cone angle of 90° is 2.5 times larger in the lateral direction (circumferential direction) while following the surface of a 110℃ truncated conical mandrel that has been satin-finished to have an unevenness of 0.5μ. While stretching, the biaxially stretched film is stretched 3.0 times in the longitudinal direction, and then an air ring with a diameter of 350φ and a lip gap of 3mm is placed around the entire outer circumference of the biaxially stretched film that has left the mandrel and is in a tubular state, at a position 50mm from the lower end of the mandrel. At the same time, air at 15℃ and 10m/sec is blown into the inside of the tubular film through the conduit at the bottom end of the mandrel.
A tubular biaxially stretched breathable film was obtained by continuously blowing at a rate of 40 Nl/m 2 ·min to continuously penetrate the film in the thickness direction from the inside to the outside, and then taking it off with a Nippro roll. . Table 1 shows the appearance and physical properties of the breathable film obtained. The moisture permeability is JIS Z0208, and the air permeability is
JIS P8117 and tear strength were measured based on JIS Z1702. Example 2 In Example 1, ethylene-propylene-butene-1 copolymer (density 0.918 g/cm 3 , MFR 0.701 g/cm 3 ) was used instead of ethylene-butene-1 copolymer.
10 minutes, using a powder with a Q value of 6 and a melting point of 123℃,
Cooling air blowing of tubular biaxially stretched film 5
A breathable film was obtained in the same manner as in Example 1, except that the air blowing rate was 20 Nl/m 2 ·min. The results of the obtained breathable film are also shown in Table 1. Comparative Example 1 In Example 1, density 0.920g/cm 3 , MFR 1.0
g/10 minutes, using an ethylene-butene-1 copolymer with a Q value of 3.4 and a melting point of 124°C, with the preheating temperature and stretching temperature adjusted.
Stretched under the same conditions as Example 1 except that the temperature was 113°C.
A breathable film was produced. The results are also shown in Table 1. Comparative Example 2 In Example 1, high density polyethylene (density 0.950
g/cm 3 , MFR 0.05 g/10 min, melting point 132°C) was pelletized at 290°C, extruded as a tubular unstretched film at 260°C, and the preheating temperature and stretching temperature were changed to 118°C. The film was stretched under the same conditions as in Example 1 to obtain a breathable film. The results are also shown in Table 1. 【table】
Claims (1)
ートが0.1〜5g/10分、数平均分子量に対する
重量平均分子量の比で表されるQ値が4以上であ
るエチレン−α−オレフイン共重合体42〜87体積
%と無機充填剤58〜13体積%との組成物からなる
管状未延伸フイルムを円錐台形のマンドレルに沿
わせながら二軸延伸し、引き続き、管状二軸延伸
フイルムの外側から気体を吹付けることにより該
フイルムを冷却すると共に、該フイルムの内側か
ら連続的に気体を吹込むことにより該フイルムの
外側に貫通させることを特徴とする通気性フイル
ムの製造方法。1 Ethylene-α-olefin copolymer having a density of 0.910 to 0.940 g/cm 3 , a melt flow rate of 0.1 to 5 g/10 min, and a Q value expressed as the ratio of weight average molecular weight to number average molecular weight of 4 or more A tubular unstretched film made of a composition of 42 to 87% by volume and an inorganic filler of 58 to 13% by volume is biaxially stretched along a truncated conical mandrel, and then gas is introduced from the outside of the tubular biaxially stretched film. A method for producing a breathable film, which comprises cooling the film by blowing the film, and penetrating the film to the outside by continuously blowing gas from the inside of the film.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58113484A JPS606440A (en) | 1983-06-23 | 1983-06-23 | Manufacture of gas-permeable film |
| US06/620,828 US4585604A (en) | 1983-06-23 | 1984-06-15 | Process for preparing an air-permeable film |
| GB08415472A GB2143772B (en) | 1983-06-23 | 1984-06-18 | Preparing air-permeable thermoplastic film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58113484A JPS606440A (en) | 1983-06-23 | 1983-06-23 | Manufacture of gas-permeable film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS606440A JPS606440A (en) | 1985-01-14 |
| JPH0314059B2 true JPH0314059B2 (en) | 1991-02-25 |
Family
ID=14613451
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58113484A Granted JPS606440A (en) | 1983-06-23 | 1983-06-23 | Manufacture of gas-permeable film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS606440A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06104733B2 (en) * | 1986-07-16 | 1994-12-21 | 住友化学工業株式会社 | Breathable film and manufacturing method thereof |
-
1983
- 1983-06-23 JP JP58113484A patent/JPS606440A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS606440A (en) | 1985-01-14 |
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