JPH03199412A - Ultrafine acrylic fiber - Google Patents

Ultrafine acrylic fiber

Info

Publication number
JPH03199412A
JPH03199412A JP34429589A JP34429589A JPH03199412A JP H03199412 A JPH03199412 A JP H03199412A JP 34429589 A JP34429589 A JP 34429589A JP 34429589 A JP34429589 A JP 34429589A JP H03199412 A JPH03199412 A JP H03199412A
Authority
JP
Japan
Prior art keywords
spinning
acrylonitrile
fibers
molecular weight
weight
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
JP34429589A
Other languages
Japanese (ja)
Inventor
Yoshihiro Nishihara
良浩 西原
Yoshihiko Hosako
宝迫 芳彦
Taku Tabuchi
田渕 卓
Hideki Moriishi
森石 英樹
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Rayon 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 Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP34429589A priority Critical patent/JPH03199412A/en
Publication of JPH03199412A publication Critical patent/JPH03199412A/en
Pending legal-status Critical Current

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  • Artificial Filaments (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)

Abstract

PURPOSE:To provide the subject fiber composed of an acrylonitrile-based polymer having a high molecular weight, having single yarn fineness of >=a specified value, excellent in gloss, smoothness and lightweightness and capable of production of nonwoven fabrics and woven fabrics excellent in wiping properties and water retention and useful as a towel. CONSTITUTION:An objective fiber composed of an acrylonitrile-based polymer (preferably containing acrylonitrile in an amount of >=80wt.%) having >=200000 weight-average molecular weight and having <=0.05d single yarn fineness.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は単繊維繊度が0.05 d以下の極細アクリル
繊維に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to ultrafine acrylic fibers having a single fiber fineness of 0.05 d or less.

〔従来の技術〕[Conventional technology]

アクリル繊維はその優れた繊維物性、例えば発色性、鮮
明性及び堅牢性などの染色性、耐光性、耐食性などに優
れた繊維として知られ、衣料用途、インテリア用途を中
心に広く利用されている。通常アクリル繊維は、湿式紡
糸法、乾湿式紡糸法或いは乾式紡糸法で作られるが、こ
れらの紡糸方法ではいずれも重合体を溶剤に溶解[7た
紡糸原液を紡糸ノズルより吐出して繊維に賦型した後、
脱溶媒するといった非常に複雑な工程を必要とするのが
特徴である。
Acrylic fibers are known for their excellent physical properties, such as color development, brightness, fastness, light fastness, and corrosion resistance, and are widely used in clothing and interior applications. Usually, acrylic fibers are made by wet spinning, dry-wet spinning, or dry spinning, but in all of these spinning methods, the polymer is dissolved in a solvent [7] and the spinning stock solution is discharged from a spinning nozzle to impart it to the fiber. After molding,
It is characterized by requiring extremely complicated steps such as desolvation.

一方、一般に繊維を細くすると紡糸工程にて、紡糸ロー
ラー、糸ガイド等への巻きつき、毛羽立ち等が発生し易
いため複合紡糸の技術を応用し、例えば−旦紡糸した繊
維を後処理によって分割したり、また海島状の繊維とし
た後、海成分を溶出し、島成分のみを残すといった手法
が用いられている。
On the other hand, in general, when fibers are made thinner, they tend to wrap around spinning rollers, yarn guides, etc. and become fluffy during the spinning process. Alternatively, a method is used in which the sea-island-shaped fiber is made, and then the sea component is eluted, leaving only the island component.

ナイロン、ポリエステル等の溶融紡糸では工程が簡単な
ため、このような手法によって極細繊維を得ることが可
能であるが、アクリル繊維の場合には、その紡糸工程が
複雑なため、複合紡糸による手法によっても極細繊維を
製造することは困難であった。
Melt spinning of nylon, polyester, etc. is a simple process, so it is possible to obtain ultrafine fibers using this method.However, in the case of acrylic fibers, the spinning process is complicated, so it is difficult to obtain ultrafine fibers using composite spinning. However, it was difficult to produce ultrafine fibers.

したがって極細アクリル繊維を製造するには、通常の衣
料用アクリル繊維製造技術の延長線上で紡糸ノズルの口
径を小さくしたり、また、延伸倍率を高くするといった
手法で繊度を細くする方法をとらざるを得ないが、この
ような方法でも高々、単繊維繊度が0.1d程度の細さ
を得るのが限界である。
Therefore, in order to manufacture ultra-fine acrylic fibers, it is necessary to reduce the fineness by reducing the diameter of the spinning nozzle and increasing the drawing ratio, which is an extension of the conventional manufacturing technology for acrylic fibers for clothing. However, even with this method, the limit is to obtain a single fiber fineness of about 0.1 d.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

本発明の目的は、従来の方法では製造し得ない0.05
 d以下の極細アクリル繊維を提供することにある。
The purpose of the present invention is to obtain 0.05
The purpose of the present invention is to provide ultrafine acrylic fibers with a diameter of d or less.

〔課題を解決するための手段〕[Means to solve the problem]

本発明は、重量平均分子量が20万以上のアクリロニト
リル系重合体からなる単繊維繊度が0、05 d以下の
極細アクリル繊維にある。
The present invention is directed to an ultrafine acrylic fiber having a single fiber fineness of 0.05 d or less and made of an acrylonitrile polymer having a weight average molecular weight of 200,000 or more.

本発明の極細アクリル繊維を製造するために用いるアク
リロニ) IJル系重合体は、その重量平均分子量が2
0万以上であることが必要である。極細アクリル繊維を
製造するためには、紡糸原液中のアクリロニトリル系重
合体濃度を下げ、また、紡糸ノズルからの紡糸原液の吐
出線速度と未延伸糸の速度の比、いわゆる紡糸ドラフト
をできるだけ高くする方法が用いられる。
The acrylonitrile (IJ) polymer used to produce the ultrafine acrylic fiber of the present invention has a weight average molecular weight of 2.
It must be 00,000 or more. In order to produce ultra-fine acrylic fibers, it is necessary to lower the acrylonitrile polymer concentration in the spinning dope and to increase the ratio of the linear velocity of the spinning dope from the spinning nozzle to the speed of the undrawn yarn, the so-called spinning draft, as much as possible. method is used.

したがって、紡糸原液中のアクリロニ)Ifル系重合体
の濃度は10重量%以下に設定するのが好ましいが、用
いる重合体の重量平均分子量が20万未満の場合には、
このような低濃度の紡糸原液を調製しても、その粘度が
低くなり曳糸性が発現しなくなるため、安定に紡糸を続
けることが不可能である。
Therefore, it is preferable to set the concentration of the acryloni)If-based polymer in the spinning dope to 10% by weight or less, but if the weight average molecular weight of the polymer used is less than 200,000,
Even if such a low-concentration spinning stock solution is prepared, it is impossible to continue spinning stably because its viscosity becomes low and spinnability is no longer expressed.

また、本発明で用いるアクリロニトリル系重合体は得ら
れる繊維の物性の点からアクリロニトリルを80重量%
以上含有していることが必要である。また、アクリルニ
トリルに共重合させる共重合成分としては例えばアクリ
ル酸、メタクリル酸、メチルアクリレート又はメタクリ
レート、エチルアクリレート又はメタクリレート、n−
イソ−1又はt−ブチルアクリレート又はメタクリレー
ト、2−エチルへキシルアクリレート又はメタクリレー
ト、α−クロロアクリロニトリル、2−ヒドロキシエチ
ル了クリレート又はメタクリレート、ヒドロキシアル手
ルアクリレート又はメタクリレート、塩化ビニル、塩化
ビニリデン、臭化ビニリデン、酢酸ビニル、p−スルホ
フェニルメタリルエーテルのナトリウム塩、メタリルス
ルホン酸ナトリウム等の不飽和単量体が挙げられるが、
アクリロニトリルと共重合しつる単量体ならいずれの単
量体でもよく、2種以上の単量体を併用することもでき
る。本発明で用いる重量平均分子量が20万以上のアク
リロニトリル系重合体は懸濁重合法によって得ることが
できる。
In addition, the acrylonitrile polymer used in the present invention contains 80% by weight of acrylonitrile in view of the physical properties of the fibers obtained.
It is necessary to contain the above amount. Examples of copolymerization components to be copolymerized with acrylonitrile include acrylic acid, methacrylic acid, methyl acrylate or methacrylate, ethyl acrylate or methacrylate, n-
Iso-1 or t-butyl acrylate or methacrylate, 2-ethylhexyl acrylate or methacrylate, α-chloroacrylonitrile, 2-hydroxyethyl acrylate or methacrylate, hydroxyalkyl acrylate or methacrylate, vinyl chloride, vinylidene chloride, bromide Examples include unsaturated monomers such as vinylidene, vinyl acetate, sodium salt of p-sulfophenyl methallyl ether, sodium methallyl sulfonate, etc.
Any monomer that copolymerizes with acrylonitrile may be used, and two or more types of monomers may be used in combination. The acrylonitrile polymer having a weight average molecular weight of 200,000 or more used in the present invention can be obtained by a suspension polymerization method.

次にこのようなアクリロニトリル系重合体をジメチルホ
ルムアミド、ジメチルアセトアミド、ジメチルスルホキ
シド、ロダン塩水溶液、塩化亜鉛水溶液等の溶剤に溶解
する。続いて紡糸原液を目開きが10μ以下のる材でろ
過し、紡糸ノズルより吐出させる。紡糸ノズルの口径は
小さいなど好ましく、50μ以下、好ましくは40μ以
下の口径の紡糸ノズルを使用するのがよい。紡糸方式と
しては紡糸ノズルより紡糸原液を凝固浴中に吐出する湿
式紡糸が好ましく用いられる。凝固浴としては一般にア
クリロニトリル系重合体の溶媒と水の混合液を用いる。
Next, such an acrylonitrile polymer is dissolved in a solvent such as dimethylformamide, dimethylacetamide, dimethyl sulfoxide, rhodan salt aqueous solution, zinc chloride aqueous solution, or the like. Subsequently, the spinning stock solution is filtered through a material with an opening of 10 μm or less, and is discharged from a spinning nozzle. The diameter of the spinning nozzle is preferably small, and it is preferable to use a spinning nozzle with a diameter of 50 μm or less, preferably 40 μm or less. As the spinning method, wet spinning in which a spinning stock solution is discharged into a coagulation bath from a spinning nozzle is preferably used. The coagulation bath is generally a mixture of an acrylonitrile polymer solvent and water.

このようにして得られた凝固糸は引き続き残留した溶剤
を洗浄、除去しながら延伸を施す。延伸方法としては洪
水中での延伸または延伸倍率を高く設定し繊度を細くす
るために、洪水延伸と熱ロール又は熱板、又は加熱チュ
ーブ等を組み合わせておこなうのがよい。
The coagulated thread thus obtained is subsequently drawn while washing and removing the remaining solvent. As for the stretching method, it is preferable to use a combination of flood stretching and hot rolls, hot plates, heating tubes, etc. in order to set a high stretching ratio and reduce the fineness.

また一般に単繊維繊度を小さくすると凝固浴中での糸切
れや紡糸ローラー、糸ガイド等への巻きつきが多発し、
工程通過性が悪くなるが、驚くべきことに本発明の極細
アクリル繊維は単繊維間のからみ合いが多いため、その
集束性が非常に良好であり、そのため紡糸ローラーや糸
ガイド上で、紡糸糸条の分繊による単繊維切れはほとん
ど発生しないため工程通過性は非常に良好である。
In general, when the single fiber fineness is reduced, thread breakage in the coagulation bath and winding around spinning rollers, thread guides, etc. occur frequently.
However, surprisingly, the ultrafine acrylic fiber of the present invention has very good cohesiveness due to the large number of intertwining between single fibers, and therefore, it is possible to easily collect the spun yarn on the spinning roller or yarn guide. Since there is almost no single fiber breakage due to fiber splitting, processability is very good.

〔発明の効果〕〔Effect of the invention〕

以上の方法で製造できる本発明の単繊維繊度が0.05
 d以下の極細アクリル繊維は、従来のアクリル繊維で
は得られない光沢と柔らかさ、軽さを有する。また、繊
維重量当りの表面積も従来のアクリル繊維に比較して大
幅に増すことから、例えば不織布や織物を作成した場合
、ワイピング性能も大きく向上し、更に保水率も大きく
向上することからタオル、ワキン用の繊維としても非常
に有効である。
The single fiber fineness of the present invention that can be produced by the above method is 0.05.
Ultrafine acrylic fibers with a diameter of d or less have gloss, softness, and lightness that cannot be obtained with conventional acrylic fibers. In addition, the surface area per fiber weight is significantly increased compared to conventional acrylic fibers, so when non-woven fabrics and textiles are created, for example, the wiping performance is greatly improved, and the water retention rate is also greatly improved, so towels, washing machines, etc. It is also very effective as a fiber for commercial purposes.

〔実施例〕〔Example〕

以下、実施例により本発明を具体的に説明する。 Hereinafter, the present invention will be specifically explained with reference to Examples.

なお、重量平均分子量(Mw)はジメチルホルムアミド
を溶媒として25℃にて重合体の極限粘度を測定し、次
式によって算出した値である。
Note that the weight average molecular weight (Mw) is a value calculated by the following formula by measuring the intrinsic viscosity of the polymer at 25° C. using dimethylformamide as a solvent.

[η] = 3.35 x  10−’ [Mwl 0
°72実施例、比較例 懸濁重合法で重量平均分子、ttL5万、3o万で、か
つアクリロニl−IJル/酢酸ビニル−92/8 (重
量%)のアクリロニトリル系重合体を得た。各重合体を
用い以下の条件で湿式紡糸した。
[η] = 3.35 x 10-' [Mwl 0
72 EXAMPLES AND COMPARATIVE EXAMPLES An acrylonitrile polymer having a weight average molecular weight of 50,000 ttL and 30,000 ttL and acrylonitrile/vinyl acetate 92/8 (wt%) was obtained by suspension polymerization. Wet spinning was performed using each polymer under the following conditions.

なお、上記番号1〜4は比較例、番号5〜8は本発明を
示す。
Note that the numbers 1 to 4 above indicate comparative examples, and the numbers 5 to 8 indicate the present invention.

次いで、得られた繊維を開綿し、ガラス板上につけた指
紋を何回でふき取れるか調べた。
Next, the obtained fibers were opened to see how many times it would take to wipe off fingerprints left on a glass plate.

番号  単繊維繊度(d)  拭取回数(回)番号 単繊維繊度(d) 保水率(%) 03.0(市販アクリル繊維)      13.25
          0.05           
    42.58          0、01  
             5(1,10,1 0,05 0,03 0,01 単繊維繊度が小さいほうがワイピング性能は良好であっ
た。
Number Single fiber fineness (d) Number of wiping (times) Number Single fiber fineness (d) Water retention rate (%) 03.0 (commercially available acrylic fiber) 13.25
0.05
42.58 0, 01
5(1,10,1 0,05 0,03 0,01 The smaller the single fiber fineness was, the better the wiping performance was.

また、得られた繊維を用い保水率を測定した。Furthermore, the water retention rate was measured using the obtained fibers.

保水率の測定は以下の方法でおこなった。The water retention rate was measured using the following method.

常法により精練した繊維を水中に24時間浸せきした後
、1000Gの加速度のもとて10分間脱水した原綿の
重量をW、とする。
The weight of the raw cotton obtained by immersing fibers refined in a conventional manner in water for 24 hours and dewatering them for 10 minutes under an acceleration of 1000 G is defined as W.

この繊維を110℃で3時間熱風乾燥した後の重量をW
2とし次式より算出した。
After drying this fiber with hot air at 110℃ for 3 hours, the weight is W
2 and calculated from the following formula.

四2Four two

Claims (1)

【特許請求の範囲】[Claims] 重量平均分子量が20万以上のアクリロニトリル系重合
体からなる単繊維繊度が0.05d以下の極細アクリル
繊維。
Ultra-fine acrylic fiber with a single fiber fineness of 0.05d or less, made of an acrylonitrile polymer with a weight average molecular weight of 200,000 or more.
JP34429589A 1989-12-27 1989-12-27 Ultrafine acrylic fiber Pending JPH03199412A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34429589A JPH03199412A (en) 1989-12-27 1989-12-27 Ultrafine acrylic fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34429589A JPH03199412A (en) 1989-12-27 1989-12-27 Ultrafine acrylic fiber

Publications (1)

Publication Number Publication Date
JPH03199412A true JPH03199412A (en) 1991-08-30

Family

ID=18368136

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34429589A Pending JPH03199412A (en) 1989-12-27 1989-12-27 Ultrafine acrylic fiber

Country Status (1)

Country Link
JP (1) JPH03199412A (en)

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