JPS5841909A - Production of extremely fine fiber - Google Patents

Production of extremely fine fiber

Info

Publication number
JPS5841909A
JPS5841909A JP13678181A JP13678181A JPS5841909A JP S5841909 A JPS5841909 A JP S5841909A JP 13678181 A JP13678181 A JP 13678181A JP 13678181 A JP13678181 A JP 13678181A JP S5841909 A JPS5841909 A JP S5841909A
Authority
JP
Japan
Prior art keywords
organic substance
extruder
organic
substance
rod
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
JP13678181A
Other languages
Japanese (ja)
Inventor
Masamitsu Nagahama
正光 長浜
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.)
Pentel Co Ltd
Original Assignee
Pentel 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 Pentel Co Ltd filed Critical Pentel Co Ltd
Priority to JP13678181A priority Critical patent/JPS5841909A/en
Publication of JPS5841909A publication Critical patent/JPS5841909A/en
Pending legal-status Critical Current

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  • Multicomponent Fibers (AREA)

Abstract

PURPOSE:A dispersion consisting of two kinds of organic substances with different viscosity in an extruder is passed through a plurality of microholes and the filaments are integrated, then one of the organic substance is removed by melting, thus producing fine and long filaments of the organic substance easily. CONSTITUTION:An organic substance of high viscosity in an extruder A such as nylon 6 and another organic substance of low viscosity such as acrylonitrile- styrene copolymer B are kneaded and the resultant dispersion is passed through a plurality of microholes by a hydraulic pressure, e.g., by means of a ram extruder at a low rate of plunger movement. After passage of the microholes, the organic substance B is integrated and taken out of the outlet of the extruder as a rod. Then, the rod is treated with a solvent for the organic substance B to remove the substance B and obtain fine filaments of the substance A.

Description

【発明の詳細な説明】 本発明は細く、シかも、長い繊維を製造する方法に関す
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing fine, thin and long fibers.

従来、細い繊維を得る方法としては、I!#公昭44−
183tS9号公報に係る海鳥型複合繊維のi成分を溶
解除去する方法をはじめ9種々提案されて−るが、押出
機の口金部分に煩わしい改良を施さなければならなかっ
たり、長い繊維が得られなかったりするという問題があ
った。
Conventionally, as a method for obtaining thin fibers, I! # Kosho 44-
Nine different methods have been proposed, including the method of dissolving and removing the i component of seabird-type composite fibers as disclosed in Publication No. 183tS9, but these methods require cumbersome improvements to the extruder nozzle, and long fibers cannot be obtained. There was a problem that

そこで1本発明は容易に細くて長い繊維を得んことを目
的になされたものであり、押出機内の高粘度状態にある
有機物Aと低粘度状態にある有機物Bとのマクロ分散物
を静水圧的力によって複数のミクロ孔に通し、谷ミクロ
孔通過後の有機物Bを一体化させ、押出機開口椿より棒
状体に取り出し、棒状体中の有機物Bを溶解除去するこ
とによる有機物Aの極細繊維の製造り法を要旨とするも
のである。
Therefore, the present invention was made with the aim of easily obtaining thin and long fibers, and a macro dispersion of organic substance A in a high viscosity state and organic substance B in a low viscosity state in an extruder is heated by hydrostatic pressure. Ultrafine fibers of organic substance A are produced by passing the organic substance B through multiple micropores by mechanical force, integrating the organic substance B after passing through the valley micropores, taking it out into a rod-shaped body from the extruder opening, and dissolving and removing the organic substance B in the rod-shaped body. The gist is the manufacturing method.

本発明に使用される有機物A、Hとしては。The organic substances A and H used in the present invention are as follows.

ポリアミド(ナイロン6、ナイロン12.ナイロン66
、ナイロン610.ポリメタキシレンアジパミドなど)
、ポリオレフィン(ポリエチレン、ポリプロピレンなど
)、ポリエステル(ポリエチレンテレフタレート、ポリ
ブチレンテレフタレートなど)、ポリ塩化ビニル、ポリ
塩化ビニリデン、ポリアクリロニトリル、アクリロニト
リルスチレン共重合物、アクリロニトリルブタジェンス
チレン共重合物、ポリウレタン、ポリビニルアルコール
、ポリ酢酸ビニルなど及びそれらの共重合物や、パラフ
ィンワックスなどの1種もしくは2種以上の組み合わせ
が例示できるが、有機物Aと有機物Bとの組み合わせと
しては、互いに相溶性がなく、同一条件において、有機
物Bの方が低粘度状態になるものを選択しなければなら
ない。従って、有機物Bの方が低融点のものを使用する
か、可塑剤や溶剤などを用い低粘度化させるが、ここで
いう低(高)粘度状態とは、一定圧力を加えられたとき
の流れ易さ状態を意、味するものであハ厳密な「粘性」
以外の他特性を付随していてもよいものである。
Polyamide (nylon 6, nylon 12, nylon 66
, nylon 610. polymethaxylene adipamide, etc.)
, polyolefins (polyethylene, polypropylene, etc.), polyesters (polyethylene terephthalate, polybutylene terephthalate, etc.), polyvinyl chloride, polyvinylidene chloride, polyacrylonitrile, acrylonitrile styrene copolymer, acrylonitrile butadiene styrene copolymer, polyurethane, polyvinyl alcohol, Examples include polyvinyl acetate, copolymers thereof, paraffin wax, etc., or combinations of two or more, but as a combination of organic substance A and organic substance B, they are not compatible with each other, and under the same conditions, Organic substance B must be selected to have a lower viscosity. Therefore, for organic substance B, one with a lower melting point is used, or the viscosity is lowered by using a plasticizer or solvent, but the low (high) viscosity state here refers to the flow when a constant pressure is applied. It means and tastes the state of ease, and is strictly "viscosity".
It may also be accompanied by other characteristics.

適宜割合で使用される有機物Aと有機物Bとは必要に応
じ使用される可塑剤などの他の添加剤とともに混練され
1分散物となる。この際。
Organic substance A and organic substance B used in an appropriate ratio are kneaded together with other additives such as a plasticizer used as necessary to form a single dispersion. On this occasion.

予め有機物AやBK添加剤を混入しておいても工い。分
散物は有機物A相がなるべく大きな相となるようにする
のが好ましく、混合樹脂の一般的押出成形の場合の適度
、即ち、十分な混−練は本発明においては過度の混練と
なる。もつとも、混線方法自体は徨々存在する。例えば
、市販ベレット状物のトライブレンド、有機物Bを分散
媒とする中に塊状の有機物Aを入れ攪拌する方法、その
他力ツタ−によって攪拌する方法などであり、必要に応
じ適宜加熱する。
You can also mix organic substance A and BK additives in advance. It is preferable that the organic substance A phase of the dispersion is as large as possible, and moderate or sufficient kneading in the case of general extrusion molding of mixed resins becomes excessive kneading in the present invention. However, there are many methods of crosstalk. For example, there is a triblend of commercially available pellets, a method in which a lump of organic material A is placed in organic material B as a dispersion medium and stirred, and another method in which stirring is performed using a power stirrer, with appropriate heating as required.

分散物をミクロ孔に通す場合、その力は実質的に静水圧
的でなければならない。従って、押出機としてはラム式
を用いるのがよく、スクリュ一式を用いる場合にはスク
リューの回転数を遅くさせる必要がある。即ち、スクリ
ュ一式の場合、有機物A、Hの種類及びその状態並びに
押出機の構造によって異なる為、−概に範囲を決定する
ことはできないが2通常の繊維を製造する場合の百以下
、好ましくは角取下の回転数にすることを目処とされた
い。尚、スクリュ一式の場合、このようにスクリューの
回転数を小さくすることは混線が過度となることを防止
することKもなる。
When forcing the dispersion through the micropores, the force must be substantially hydrostatic. Therefore, it is preferable to use a ram type extruder, and when a screw set is used, it is necessary to slow down the rotational speed of the screw. In other words, in the case of a set of screws, it varies depending on the type and state of the organic substances A and H and the structure of the extruder, so the range cannot be determined generally, but it is preferably less than 100 when producing ordinary fibers. The goal is to get the rotation speed down to the corner level. In the case of a set of screws, reducing the number of rotations of the screws in this way also prevents excessive crosstalk.

また、複数個存在するミクロ孔は2分散物の全体として
の流れに対しなるべく垂直に配設されるのが好ましく、
逆に1円筒体の周壁に設けられた複数のミクロ孔を通過
させるようなことは決して好ましくなめ、これは1分散
物がミクロ孔を通過するときに有機物A+Bを切断する
方向の力を生じることKなるからであり、得られる繊維
が短かくなってしまう。尚、ミクロ孔はlijうとする
繊維の太さを決定する。少くとも1つの要因となるもの
であり、その名が示すように例えば100 pmとか1
0 pmといったように(勿論より、大きくても、また
、より小さくてもよい)小さな孔であり2通常、極めて
多数のミクロ孔が存在する1例えばメツシュのようなも
のを使用するが、他に誂えられたものであってもよい。
Further, it is preferable that the plurality of micropores are arranged perpendicularly to the overall flow of the two dispersions,
On the other hand, it is never preferable to pass the dispersion through multiple micropores provided on the peripheral wall of a cylindrical body, as this may generate a force in the direction of cutting the organic matter A+B when the dispersion passes through the micropores. This is because the fibers obtained become short. Note that the micropores determine the thickness of the fiber to be lijed. It is at least one factor, and as the name suggests, for example, 100 pm or 1
The pores are small, such as 0 pm (of course, they can be larger or smaller). 2 Usually, a very large number of micropores are present. 1 For example, a mesh is used, but there are other It may be custom-made.

=5− ミクロ孔を通る際、有機物Aは孔中心部を通り、有機物
Bは孔壁部を通り、有機物Aを有機物Bが被覆する形で
出てくる。また、有機物Bはいずれのミクロ孔をも通る
のに対し、有機物Aはいったん通り始めたミクロ孔を選
択的に通過する。勿論、有機物Aが唯一のミクロ孔のみ
を通るというのではないが、この傾向が存在する。他の
条件を同一にしたとき、有機物Aが通るミクロ孔の数は
1分散物の流速に影響を受ける。即ち、流速が早ければ
早い程1通るミクロ\− ランジャーの移動速度を、また、スクリュ一式の場合は
スクリューの回転速度を、それぞれ小さくすることが得
られる繊維の長さをより長くするのに役豆つ。
=5- When passing through the micropore, organic matter A passes through the center of the pore, organic matter B passes through the pore wall, and comes out in a form where organic matter A is covered with organic matter B. Further, while organic substance B passes through any micropore, organic substance A selectively passes through the micropore that it has started passing through. Of course, this does not mean that organic substance A passes only through the only micropore, but this tendency exists. When other conditions are kept the same, the number of micropores through which the organic substance A passes is influenced by the flow rate of the dispersion. In other words, the faster the flow rate, the faster the moving speed of the micro-lunger, or the rotational speed of the screw in the case of a set of screws, will help increase the length of the fibers obtained. Beans.

ミクロ孔を通過後、必要に応じ適宜使用されるブレーカ
−プレートなどを更に通過し、好みの径となって押出機
開口より出る。出てきたものけ適宜延伸等され、得られ
た棒状物を、有機6− 物Bの溶剤によって処理し、有機物Aの細くて長い繊維
が得られる。
After passing through the micropores, it further passes through a breaker plate, etc., which is used as needed, and exits from the extruder opening after reaching the desired diameter. The resulting rod-like material is stretched as appropriate, and the obtained rod-like material is treated with a solvent of organic substance B to obtain thin and long fibers of organic substance A.

〈実施例〉 ナイロン12(日本リルサン■より購入=40重量嘱の
活性剤が練り込まれているという)と7クリロニトリル
スチレン共重合物(アサヒダウ■よV購入:製品符号す
676)とを使用した。(使用割合(重量割合)は前@
:*考=80:20,70:30,60:40で行ない
<Example> Using nylon 12 (purchased from Nippon Rilsan ■, said to be kneaded with 40 weight parts of activator) and 7-acrylonitrile styrene copolymer (purchased by Asahi Dow ■, product code: 676) did. (Usage ratio (weight ratio) is before @
:*Consideration=80:20, 70:30, 60:40.

いずれも結果は良好だった。) 前者は略フレーク状、後者は略円柱状をしておp1両者
をまずトライブレンドした後、80℃、12時間の乾燥
で不要な水分を除去し、スクリュ一式押出機のホッパー
に入れた。使用した押出機はL/D426の急圧縮タイ
プ(ナイロン用)のスクリュー(ピッチ:40m!l、
  メジャリング部の谷−スリーブ内壁間距離:2m)
を有し、スリーブの内径は40mのものである。スリー
ブ の温度は、ホッパーからスリーブ先端に取り付けられた
ヘッドの方向に向い、約λの地点で145℃、約(の地
点で220℃、約筈の地点で233℃のレコーダー読み
取りがなされ、また、立体角が約200の略ロート状の
内壁面を有し、ロートの管にあたる部分がL字状となっ
て、地面方向に向けられた。その先端開口径が1211
のヘッドとの接点部(即ち、音の地点)では同じく23
6℃とした。
All results were good. ) The former was in the form of approximately flakes, and the latter in the form of cylinders.The two products were first triblended, and unnecessary water was removed by drying at 80° C. for 12 hours, and the mixture was placed in the hopper of a single-screw extruder. The extruder used was an L/D426 rapid compression type (for nylon) screw (pitch: 40 m!l,
Distance between valley of measuring part and inner wall of sleeve: 2m)
The inner diameter of the sleeve is 40 m. The temperature of the sleeve is oriented from the hopper to the head attached to the tip of the sleeve, and the recorder readings are 145°C at a point of about λ, 220°C at a point of (), and 233°C at a point where it should be, and It has an approximately funnel-shaped inner wall surface with a solid angle of about 200, and the part corresponding to the funnel tube is L-shaped and directed toward the ground.The diameter of the opening at the tip is 1211.
23 at the point of contact with the head (i.e., the point of sound)
The temperature was set at 6°C.

スリーブ先端、即ち、ヘッドとの接点部には。At the tip of the sleeve, that is, at the contact point with the head.

2枚の30メツシニの孔を有する厚さ約0.5 tan
の円板体にて200メツシユの厚さ約0. I mの円
板体(以上3省はアクボノメッシェ社製で製品名はハイ
スクリーン)をサンドイッチ状としスクリューの回転速
度は3.4rpm/分とし。
Approximately 0.5 tan thick with two 30 mesh holes
The thickness of 200 mesh is approximately 0. I m disk bodies (the above three parts are manufactured by Akubonomesche Co., Ltd. and the product name is Hi-Screen) were made into a sandwich shape, and the rotational speed of the screw was set to 3.4 rpm/min.

ヘッダーの先端開口から出てぐるものは自重落下に任せ
て棒状体とした。(棒状体は冷却槽のセツティングによ
り直径が28のものと1011のものを得たが、いずれ
も結果は良好だった。)試験片とする為、棒状体を40
1Jlの長さに切り出し、アクリロニトリルスチレン共
重合物の溶剤(トリクロルエチレンを使用したが、他の
塩素化系の溶剤や酢酸エステルなどのエステル系溶剤、
メチルエチルケトンなどのケトン系溶剤などナイロン1
2を溶解しないものならなんでもよい。)によってアク
リロニトリルスチレン共重合物を除去後、メタノール液
にて洗浄。
The material coming out of the opening at the end of the header was left to fall under its own weight to form a rod-shaped body. (Depending on the setting of the cooling tank, rod-shaped bodies were obtained with diameters of 28 and 1011, and the results were good in both cases.) In order to use them as test pieces, the rod-shaped bodies were
Cut into 1 Jl length, and use acrylonitrile styrene copolymer solvent (trichlorethylene was used, but other chlorinated solvents, ester solvents such as acetate,
Nylon 1 such as ketone solvents such as methyl ethyl ketone
Anything that does not dissolve 2 may be used. ) to remove the acrylonitrile styrene copolymer, then wash with methanol solution.

乾燥して、ナイロン12の繊維の多数本の束状物を得た
。得られた繊維は実質的にすべて40賜であり、これに
より少くとも40uより長い繊維の束状物が得られてい
ることが判明した。
After drying, a bundle of multiple fibers of nylon 12 was obtained. It was found that substantially all of the fibers obtained were 40 mm, thereby providing a bundle of fibers with a length of at least 40 u.

本発明は以上説明したように、容易に細くて長い繊維を
得ることができ、織物関係に有効活用できるだけでなく
、現在、高価格であることを余儀なくされているエアー
細菌用フィルター。
As explained above, the present invention not only allows easy production of thin and long fibers and can be effectively used in textiles, but also provides a filter for air bacteria, which is currently unavoidably expensive.

 9− 腎臓透析フィルターをはじめとするミクロフィルター用
材に極めて有用であり、その他、複合材料の曲げ強度、
耐摩耗性向上材といったようKm々分野の種々工業材料
に広く活用され得る。
9- It is extremely useful for microfilter materials including kidney dialysis filters, and also improves the bending strength of composite materials.
It can be widely used in various industrial materials in various fields, such as wear resistance improving materials.

大きな効果を有するものである。This has a great effect.

特許出願人 べんてる株式会社 10−Patent applicant: Bentel Co., Ltd. 10-

Claims (1)

【特許請求の範囲】[Claims] 押出様内の高粘度状態にある有機初回と低粘度状態にあ
る有機物0とのマクロ分散物を静水圧的力によって複数
のミクロ孔に通し、各ミクロ孔通過後の有機物(2)を
一体化させ、押出機開口より棒状体に取り出し、棒状体
中の有機物(6)を溶解除去することによる有機初回の
極細繊維の製造方法。
A macro-dispersion of the organic material (1) in a high viscosity state and the organic matter (0) in a low viscosity state in the extrusion mold is passed through multiple micropores by hydrostatic force, and the organic matter (2) after passing through each micropore is integrated. A method for producing ultrafine organic fibers for the first time by removing the organic matter (6) from the rod-like body by dissolving and removing it from the rod-like body.
JP13678181A 1981-08-31 1981-08-31 Production of extremely fine fiber Pending JPS5841909A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13678181A JPS5841909A (en) 1981-08-31 1981-08-31 Production of extremely fine fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13678181A JPS5841909A (en) 1981-08-31 1981-08-31 Production of extremely fine fiber

Publications (1)

Publication Number Publication Date
JPS5841909A true JPS5841909A (en) 1983-03-11

Family

ID=15183362

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13678181A Pending JPS5841909A (en) 1981-08-31 1981-08-31 Production of extremely fine fiber

Country Status (1)

Country Link
JP (1) JPS5841909A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4830565U (en) * 1971-08-14 1973-04-14
JPS5418369A (en) * 1977-07-08 1979-02-10 Tokai Seiki Kk Fire extingushing apparauts for gas lighter

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4830565U (en) * 1971-08-14 1973-04-14
JPS5418369A (en) * 1977-07-08 1979-02-10 Tokai Seiki Kk Fire extingushing apparauts for gas lighter

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