JPH036264B2 - - Google Patents

Info

Publication number
JPH036264B2
JPH036264B2 JP60127100A JP12710085A JPH036264B2 JP H036264 B2 JPH036264 B2 JP H036264B2 JP 60127100 A JP60127100 A JP 60127100A JP 12710085 A JP12710085 A JP 12710085A JP H036264 B2 JPH036264 B2 JP H036264B2
Authority
JP
Japan
Prior art keywords
fiber bundle
fiber
seconds
cross
filaments
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
Application number
JP60127100A
Other languages
Japanese (ja)
Other versions
JPS61289149A (en
Inventor
Noboru Ogino
Yoshikuni Kawai
Hirobumi Ookura
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 JP12710085A priority Critical patent/JPS61289149A/en
Publication of JPS61289149A publication Critical patent/JPS61289149A/en
Publication of JPH036264B2 publication Critical patent/JPH036264B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、新規な風合を有するアクリル系長繊
維束の製造法に関する。 アクリル系長繊維は柔軟な風合と光択、染色発
色性に優れた特徴を持ち広く賞用されているが、
麻、木綿等の天然繊維の持つシヤリ感、粗硬感、
軽量感に乏しく、春、夏物の商品の適合性に欠け
るきらいがある。アクリル系長繊維の特性を損な
うことなく、シヤリ感、軽量感を付与する方法と
しては、繊維界面を溶媒又は熱処理により、溶着
又は接着する方法あるいは繊維束断面を扁平化す
る方法等が知られている。例えば特公昭43−
12616号、特公昭44−18384号、特開昭57−101032
号、特公昭49−42880号公報等に記載の方法は広
く知られているが、実用上の問題点として後加工
工程のガイド類、トラベラー等による、捩れ、擦
れ等の外力により溶着、接着部分の分繊、分割が
進み、その効果が減少することは避けられない。
また繊維束を扁平化した場合にも特定の部分に応
力の集中が起こり、分割、ケバ立ち、ささくれ立
ち等の障害が起こり、処理速度の低下等の対応策
が強いられるが、これによる経済的損失は避けら
れない。アクリル系長繊維の後加工工程は原糸巻
き取り、撚糸、合撚、仮撚、ソフトチーズ巻き、
チーズ染色、綛染色、コーン巻き返し、編成等と
製品を得るまでの過程が長く、接着扁平糸等は特
別な取扱いを要するため、これが費用上昇の原因
となつている。特にリングワインダーを使用する
工程、仮撚等の工程は捩れ、擦れ等の外力の作用
が強く、これらの工程を避けた商品展開をせざる
を得ないのが実状である。本発明者らはこれらの
問題点を解決するために鋭意検討し、本発明を完
成した。 本発明は、乾強度2.5g/d以下のフイラメン
トより構成される繊維束を該繊維の溶媒水溶液で
処理し、1.5〜3.0倍の水溶液を含有させ、135〜
165℃、0.2〜0.6秒の短時間高温処理で急激に水
分除去を行い、さらに220〜250℃、0.3〜0.8秒の
短時間高温処理により溶着又は接着部分の接合を
強化させることを特徴とする、複数のフイラメン
トから成る30〜600デニールのアクリル系繊維束
で該繊維束の断面の経方向と緯方向の比が1:
1.0〜9.0の範囲にあり、構成フイラメントが部分
的、局所的に強固に溶着又は接着し、その割合が
30〜90%であるアクリル系長繊維束の製造法であ
る。 本発明方法によれば、高速リングワインダーに
よる巻き取り、仮撚り工程を通すことも可能であ
り、商品展開の幅の広がりが期待できる利点の
他、加工工程の生産性向上に役立てることも可能
である。 本発明のアクリル系長繊維束は、その断面を構
成する30〜90%の範囲の隣接するフイラメントが
強固に溶着又は接着されるとともに、断面内部に
好ましくは10〜40%の空隙部分を内在し、繊維束
に適度の屈曲性を有し、優れた後加工性を維持す
るものである。すなわち、10〜70%の非溶着又は
非接着部分を残すことにより、繊維束に適度の屈
曲性を与え、また空隙部分は、強い外力の作用を
受けたときにこれを緩和する働きがあり、これら
が接着又は溶着部分の分割又は分繊化を防ぐ役割
を演じている。更に部分的、局部的に、強固に溶
着又は接着された部分は繊維に剛直性を与え、風
合的にはシヤリ感を、内在する空隙部分は柔軟な
軽量感を付与することに役立つている。 本発明の繊維束の大きさは30〜600dの範囲、
繊維束断面は経方向の最大長と緯方向の最大長の
比(断面比)を1:1.0〜9.0範囲に制限すること
が必要である。600dの範囲を越えるもの又は断
面比が9.0を越えるものは、後加工工程での外力
の作用に対する耐性が弱く、ケバ立ち、糸切れの
原因となり、後加工工程の通過の悪化を招き、こ
れを防ぐため生産性の低下等の対応策が必要とな
る。 本発明に用いられる原料ポリマーはアクリロニ
トリル単独重合体又は他のビニールモノマーとの
共重合体のいずれかでもよく、これを溶解する溶
媒としては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、ロダン塩の水
溶液、硝酸水溶液等が用いられる。紡糸方式は乾
式、湿式、半乾式等のいずれかの方法でもよく、
糸条を形成させたのち、脱溶媒の工程を経て80〜
100℃の温水槽又は常圧スチーム中で2〜4倍の
延伸を加える。この工程では繊維軸方向の配向は
軽度に留め、繊維界面での溶着又は接着が短時間
で進み易い繊維構造、すなわち繊維乾強度が2.5
g/d以下、好ましくは1.8〜2.5g/dの範囲に
抑える。 次いで水膨潤状態の繊維束を水溶性又は水分散
性の繊維油剤で処理し、各構成フイラメントが次
の乾燥工程で接着しないように均一に油剤を塗布
する。この油剤付着の目的はフイラメントの接着
を防ぐとともに、ガイド類による繊維束の損傷を
防ぐためのものであり、その目的に応じ油剤の種
類、付着量、付着方法を自由に選択してよい。 次いでアクリル繊維束に対して溶解作用を有す
る溶媒の水溶液中に浸漬し、繊維束の1.5〜3.0倍
の水溶液を付着及び/又は含有させ、135〜165℃
の乾燥ローラー上で0.2〜0.6秒で瞬間的に水分の
蒸発除去を行う。 前工程の油剤処理によつて完全に分繊している
繊維束を構成する各フイラメントは、この水分除
去工程では沸騰状態のもと上下、左右に激しく振
動し、繊維内部への気泡の混入と同時に部分的、
局部的、溶着又は接着が繊維束断面に偏在するこ
となく均一に分散して進行していると推定され
る。この状態を積極的に加速化するために、過剰
の水溶液の急激な水分蒸発、構成フイラメントの
自由度を高めること及び繊維の配向を最小限に抑
えることが必要である。繊維束の保有水溶液量の
調整には通常のガイド又はニツプロールが用いら
れる。 本発明に用いられる溶媒としてはプロピレンカ
ーボネート、エチレンカーボネート、ジメチルス
ルホン、テトラメチルスルホン、ジメチルホルム
アミド、ジメチルアセトアミド、γ−ブチロラク
トン、ジメチルスルホキシド、トリメチレンカー
ボネート等の1種の水溶液又は2種以上の混合水
溶液が用いられる。ここで付与する溶媒量は溶媒
の種類による溶解力の強弱、目的とする溶着又は
接着の割合、構成フイラメント数等で異なるが、
溶媒にエチレンカーボネートを用いた150d/60f
の繊維束の場合は水溶液濃度2.2%、該繊維束の
付着水溶液量2倍で充分にその目的を達すること
ができる。 次いで水分除去した繊維束をさらに220〜250
℃、0.3〜0.8秒の短時間高温処理する。この処理
により繊維束の空隙部分を保持しながら、溶着又
は接着部分の接合を強化することができる。この
高温処理は下記の順序で行うことが好ましい。す
なわち135〜165℃℃乾燥ローラーで0.8〜2.5秒、
同じく乾燥ローラー上で165〜220℃、1.0〜3.0
秒、2段階の処理に引き続き、更に220〜250℃、
高温度に0.3〜0.8秒接触させる。この工程は溶着
又は接着をより強固にするとともに繊維内部のひ
ずみを解放する緩和の目的及び残存溶媒の加熱分
解除去又は揮発除去の意味を有する。この工程で
は繊維の着色、劣化防止の面から短時間高温処理
を行うことが必要である。 本発明に用いられる高温処理装置としては赤外
線ヒーター、高温熱風乾燥機等があげられるが、
瞬間的に繊維束に伝熱を行わせるために、ヒータ
ー内蔵型の接触熱板型の装置が好ましい。 実施例 アクリロニトリル92.7重量%、酢酸ビニール7
重量%及びメタリルスルホン酸ソーダー0.3重量
%から成る極限粘度1.60(25℃)の共重合体にジ
メチルアセトアミドを加え、固形分濃度23.5%の
紡糸原液を調整した。凝固浴液面より8mmの距離
を設けて取り付けた孔径0.12mm、孔数60holeノズ
ルより、紡糸原液を0.213ml/分・holeの速度で
吐出させながら、ジメチルアセトアミド70重量
%、温度40℃の浴中で凝固させ48.4m/分で凝固
糸を巻き取つた。次いで70℃の温水槽で、脱溶媒
を行つたのち、沸水中で3.5倍の延伸を加え180
m/分の速度とした。このとき乾強度は2.1g/
d、伸度13%であつた。次いで普通の水溶性油剤
で処理後、表面温度140℃の乾燥ローラー上で3
秒間乾燥させ、水分を完全に除去した。引き続き
2.2%エチレンカーボネート水溶液中に0.05秒浸
漬し、ニツプロールで絞り、付着水溶液量を対繊
維2.5倍に調整したのち、表面温度140℃の乾燥ロ
ーラーで0.4秒で瞬間的に全水分を除去した。次
いで乾燥ローラー表面温度140℃、1.6秒及び180
℃、2秒で2段階に分けて熱処理を実施後、235
℃の熱板上で0.6秒接触させ、3段目の熱処理を
行つた。続いて再度、対繊維2重量%の普通のス
トレート油剤を付着させ、180m/分の速度で高
速リングワインダーに巻き取つた。このときの糸
張力は、37gでスピンドルの回転数は4000rpmで
あつた。巻い取られた原糸はケバ立ち、糸切れも
なく、良好な状態であつた。また後加工性も優れ
たものであり、得られた編地はシヤリ感が強く、
軽量感に富むものであつた。得られた原糸の断面
は図面に示すように溶着又は接着部分が86.7%、
空隙率25%、断面比2.6倍であつた。 比較例 1〜3 実施例の条件を一部変更し、第1表に示す処理
を施し、原糸標本を得た。
The present invention relates to a method for producing an acrylic long fiber bundle having a novel texture. Acrylic long fibers are widely used for their soft texture, excellent photo-selectivity, and excellent dyeing and color development.
The smooth, rough and hard feel of natural fibers such as linen and cotton,
It lacks a lightweight feel and tends to be unsuitable for spring and summer products. Known methods for imparting a smooth and lightweight feel without impairing the properties of acrylic long fibers include welding or adhering the fiber interface with a solvent or heat treatment, or flattening the cross section of the fiber bundle. There is. For example, special public relations
No. 12616, Special Publication No. 18384, No. 18384, Japanese Patent Publication No. 101032, No. 1983
Although the method described in Japanese Patent Publication No. 49-42880 is widely known, there are practical problems such as welding and bonding due to external forces such as twisting and rubbing caused by guides, travelers, etc. in the post-processing process. It is inevitable that the fibers will continue to split and split, and their effectiveness will decrease.
Furthermore, when fiber bundles are flattened, stress is concentrated in specific parts, causing problems such as splitting, fluffing, and hangnails, forcing countermeasures such as reducing processing speed. Losses are inevitable. Post-processing processes for acrylic long fibers include yarn winding, twisting, plying, false twisting, soft cheese wrapping,
The process to obtain the product is long, including cheese dyeing, skein dyeing, cone winding, knitting, etc., and bonded flat yarns require special handling, which causes an increase in costs. In particular, processes that use a ring winder and processes such as false twisting are subject to strong external forces such as twisting and rubbing, and the reality is that we have no choice but to develop products that avoid these processes. The present inventors conducted extensive studies to solve these problems and completed the present invention. In the present invention, a fiber bundle composed of filaments with a dry strength of 2.5 g/d or less is treated with an aqueous solution of a solvent for the fiber, and the aqueous solution is contained in an amount of 1.5 to 3.0 times as much.
It is characterized by rapidly removing moisture through short-time high-temperature treatment at 165℃ for 0.2 to 0.6 seconds, and further strengthening the bonding of welded or bonded parts by short-time high-temperature treatment at 220 to 250℃ for 0.3 to 0.8 seconds. , an acrylic fiber bundle of 30 to 600 deniers consisting of a plurality of filaments, and the ratio of the longitudinal direction to the latitudinal direction of the cross section of the fiber bundle is 1:
It is in the range of 1.0 to 9.0, and the constituent filaments are partially and locally strongly welded or bonded, and the ratio is
This is a method for producing acrylic long fiber bundles with a content of 30 to 90%. According to the method of the present invention, it is possible to wind the material using a high-speed ring winder and pass through the false twisting process, which has the advantage of expanding the range of products available, and can also be used to improve the productivity of the processing process. be. In the acrylic long fiber bundle of the present invention, 30 to 90% of adjacent filaments constituting its cross section are firmly welded or bonded, and preferably 10 to 40% of voids are present within the cross section. The fiber bundle has appropriate flexibility and maintains excellent post-processability. In other words, by leaving 10 to 70% of the non-welded or non-bonded part, the fiber bundle is given appropriate flexibility, and the void part has the function of relieving strong external force when it is applied. These play the role of preventing the adhesion or welding portion from splitting or splitting. Furthermore, the parts that are strongly welded or glued locally and locally give the fibers rigidity and give them a smooth feel, while the internal voids help give them a soft and lightweight feel. . The size of the fiber bundle of the present invention ranges from 30 to 600 d,
It is necessary for the fiber bundle cross section to limit the ratio (cross section ratio) of the maximum length in the warp direction to the maximum length in the weft direction to a range of 1:1.0 to 9.0. Items exceeding the range of 600d or those with a cross-sectional ratio exceeding 9.0 have poor resistance to external force in the post-processing process, causing fuzzing and thread breakage, and worsening the passage of the post-processing process. In order to prevent this, countermeasures such as reducing productivity are required. The raw material polymer used in the present invention may be either an acrylonitrile homopolymer or a copolymer with other vinyl monomers, and solvents for dissolving it include dimethylformamide, dimethylacetamide, dimethyl sulfoxide, an aqueous solution of rhodan salt, and nitric acid. An aqueous solution or the like is used. The spinning method may be dry, wet, semi-dry, etc.
After forming the yarn, it goes through the process of desolvation and becomes 80~
Stretch 2 to 4 times in a 100°C hot water bath or normal pressure steam. In this process, the orientation of the fiber axis direction is kept slight, and the fiber structure is such that welding or adhesion at the fiber interface can easily proceed in a short time, that is, the fiber dry strength is 2.5.
g/d or less, preferably in the range of 1.8 to 2.5 g/d. Next, the water-swollen fiber bundle is treated with a water-soluble or water-dispersible fiber oil, and the oil is applied uniformly so that the constituent filaments do not adhere to each other in the next drying process. The purpose of this oil attachment is to prevent the filament from adhering and to prevent the fiber bundle from being damaged by the guides, and the type, amount, and method of attachment of the oil may be freely selected depending on the purpose. Next, the acrylic fiber bundle is immersed in an aqueous solution of a solvent that has a dissolving effect, and the aqueous solution is attached and/or contained in an amount 1.5 to 3.0 times that of the fiber bundle, and heated at 135 to 165°C.
Moisture is removed by instantaneous evaporation on a drying roller for 0.2 to 0.6 seconds. Each filament that makes up the fiber bundle, which has been completely separated by the oil treatment in the previous process, vibrates violently in the boiling state during this water removal process, causing air bubbles to get inside the fibers. At the same time, partially
It is presumed that the local welding or adhesion progresses in a uniformly distributed manner without being unevenly distributed in the cross section of the fiber bundle. To actively accelerate this state, it is necessary to rapidly evaporate the excess water solution, increase the freedom of the constituent filaments and minimize fiber orientation. An ordinary guide or Niprol is used to adjust the amount of aqueous solution retained in the fiber bundle. Solvents used in the present invention include one type of aqueous solution or a mixed aqueous solution of two or more of propylene carbonate, ethylene carbonate, dimethylsulfone, tetramethylsulfone, dimethylformamide, dimethylacetamide, γ-butyrolactone, dimethylsulfoxide, trimethylene carbonate, etc. is used. The amount of solvent applied here varies depending on the strength of the dissolving power depending on the type of solvent, the desired rate of welding or adhesion, the number of constituent filaments, etc.
150d/60f using ethylene carbonate as solvent
In the case of a fiber bundle, an aqueous solution concentration of 2.2% and twice the amount of aqueous solution attached to the fiber bundle can sufficiently achieve the purpose. Next, the fiber bundle from which moisture has been removed is further processed for 220 to 250
℃, short time high temperature treatment for 0.3-0.8 seconds. This treatment can strengthen the bonding of the welded or bonded portions while maintaining the voids in the fiber bundle. This high temperature treatment is preferably carried out in the following order. i.e. 135-165℃℃ drying roller for 0.8-2.5 seconds,
165-220℃, 1.0-3.0 on the same drying roller
220-250℃, followed by 2-step treatment.
Contact with high temperature for 0.3-0.8 seconds. This step has the purpose of making the welding or adhesion stronger and relaxing the fiber by releasing the strain inside the fiber, and also to remove the remaining solvent by thermal decomposition or volatilization. In this step, it is necessary to perform high temperature treatment for a short time in order to color the fibers and prevent deterioration. Examples of high-temperature processing equipment used in the present invention include infrared heaters, high-temperature hot air dryers, etc.
In order to instantaneously transfer heat to the fiber bundle, a contact heating plate type device with a built-in heater is preferred. Example Acrylonitrile 92.7% by weight, vinyl acetate 7
Dimethylacetamide was added to a copolymer with an intrinsic viscosity of 1.60 (25° C.) consisting of 0.3% by weight of sodium methallylsulfonate and 0.3% by weight of sodium methallylsulfonate to prepare a spinning stock solution with a solid content concentration of 23.5%. While discharging the spinning stock solution at a speed of 0.213 ml/min/hole from a 60-hole nozzle with a hole diameter of 0.12 mm installed at a distance of 8 mm from the coagulation bath liquid level, a bath containing 70% dimethylacetamide and a temperature of 40°C was The coagulated thread was coagulated inside the machine and wound at a speed of 48.4 m/min. Next, the solvent was removed in a hot water bath at 70°C, and then stretched 3.5 times in boiling water to 180°C.
The speed was set at m/min. At this time, the dry strength is 2.1g/
d. The elongation was 13%. Next, after treatment with a common water-soluble oil agent, it is dried on a drying roller with a surface temperature of 140℃ for 3 minutes.
It was dried for seconds to completely remove moisture. continuation
After immersing it in a 2.2% ethylene carbonate aqueous solution for 0.05 seconds and squeezing it with Nipprol to adjust the amount of adhering aqueous solution to 2.5 times that of the fiber, all moisture was instantly removed in 0.4 seconds using a drying roller with a surface temperature of 140°C. Then dry roller surface temperature 140℃, 1.6 seconds and 180℃
After heat treatment in two stages for 2 seconds at 235℃
A third heat treatment was performed by contacting them for 0.6 seconds on a hot plate at ℃. Subsequently, an ordinary straight oil agent of 2% by weight based on the fiber was applied again, and the fiber was wound on a high-speed ring winder at a speed of 180 m/min. At this time, the yarn tension was 37 g and the spindle rotation speed was 4000 rpm. The wound raw yarn was in good condition with no fluff or yarn breakage. In addition, it has excellent post-processability, and the resulting knitted fabric has a strong crisp feel.
It had a very lightweight feel. As shown in the drawing, the cross section of the obtained yarn shows that 86.7% of the yarn is welded or bonded.
The porosity was 25% and the cross-sectional ratio was 2.6 times. Comparative Examples 1 to 3 The conditions of the example were partially changed, and the treatments shown in Table 1 were performed to obtain yarn specimens.

【表】 比較例1では、高速リングワインダーにおける
巻き取り状況は良好であり、ケバ立ち、糸切れは
認められなかつた。熱処理3段目、通過後の標本
を評価したところ、溶着又は接着率は87%、断面
で2.6倍、空隙率19.4%であつた。この原糸をソ
フト巻き(約1Kg)、チーズ染色、コーン巻き返
しを経て24Gの天笠組織に編立てたのち、風合を
評価したところ、シヤリ感の少ないものであつ
た。この編地の一部を解除し、評価したところ、
溶着、接着率は28%、断面比2.2倍、空隙率8%
であり、溶着、接着率の低下が著しく、風合的に
満足すべきものは得られなかつた。 比較例2では高速リングワインダーの巻き取り
におけるケバ立ち、糸切れが多く、巻き取りが不
可能であつた。糸張力を40〜50g、スピンドル回
転数3000〜4000rpmに変更したが、いずれもケバ
立ち、糸切れを抑えることができなかつた。熱処
理3段目の標本を評価したところ、断面比10倍、
溶着、接着率92%、空隙率16%であり、断面比が
大ききく巻き取りの障害となつた。 比較例3では原糸の剛直性が強く、高速リング
ワインダーのトラベラー部分でケバが多発し、満
足すべき結果は得られなかつた。この原糸の断面
比3.2倍、溶着、接着率は97%、空隙率13%であ
り、溶着、接着率が高く、剛直性の強いものであ
つた。
[Table] In Comparative Example 1, the winding condition in the high-speed ring winder was good, and no fuzz or thread breakage was observed. When the specimen was evaluated after passing through the third stage of heat treatment, the welding or adhesion rate was 87%, the cross section was 2.6 times higher, and the porosity was 19.4%. After soft winding (approximately 1 kg), cheese dyeing, and cone winding, this raw yarn was knitted into a 24G Amagasa weave, and the texture was evaluated and found to be less stiff. When we removed a part of this knitted fabric and evaluated it,
Welding, adhesion rate is 28%, cross section ratio is 2.2 times, porosity is 8%
However, the welding and adhesion rates were significantly reduced, and a satisfactory texture could not be obtained. In Comparative Example 2, there were many fluffs and thread breaks during winding with a high-speed ring winder, and winding was impossible. Although the yarn tension was changed to 40 to 50 g and the spindle rotation speed was changed to 3000 to 4000 rpm, it was not possible to suppress fuzzing and yarn breakage. When the specimen in the third stage of heat treatment was evaluated, the cross-sectional ratio was 10 times larger;
The welding rate was 92%, the porosity was 16%, and the large cross-sectional ratio was an obstacle to winding. In Comparative Example 3, the raw yarn had strong rigidity, and fluff frequently occurred in the traveler portion of the high-speed ring winder, so that satisfactory results could not be obtained. This yarn had a cross-sectional ratio of 3.2 times, a welding and adhesion rate of 97%, and a porosity of 13%, and had a high welding and adhesion rate and strong rigidity.

【図面の簡単な説明】[Brief explanation of drawings]

図面は、実施例で得られた繊維束の拡大断面図
である。
The drawing is an enlarged cross-sectional view of a fiber bundle obtained in an example.

Claims (1)

【特許請求の範囲】[Claims] 1 乾強度2.5g/d以下のフイラメントより構
成される繊維束を該繊維の溶媒水溶液で処理し、
1.5〜3.0倍の水溶液を含有させ、135〜165℃、0.2
〜0.6秒の短時間高温処理で急激に水分除去を行
い、さらに220〜250℃、0.3〜0.8秒の短時間高温
処理により溶着又は接着部分の接合を強化させる
ことを特徴とする、複数のフイラメントから成る
30〜600デニールのアクリル系繊維束で、該繊維
束の断面の経方向と緯方向の比が1:1.0〜9.0の
範囲にあり、構成フイラメントが部分的、局所的
に強固に溶着又は接着し、その割合が30〜90%で
あるアクリル系長繊維束の製造法。
1. A fiber bundle composed of filaments with a dry strength of 2.5 g/d or less is treated with an aqueous solvent solution of the fiber,
Contain 1.5 to 3.0 times the aqueous solution, 135 to 165℃, 0.2
Multiple filaments that are characterized by rapidly removing moisture with a short-time high temperature treatment of ~0.6 seconds, and further strengthening the bonding of welded or bonded parts by a short-time high temperature treatment of 220-250℃ for 0.3-0.8 seconds. consists of
An acrylic fiber bundle of 30 to 600 deniers, the ratio of the longitudinal direction to the latitudinal direction of the cross section of the fiber bundle is in the range of 1:1.0 to 9.0, and the constituent filaments are strongly welded or bonded locally. , a method for producing acrylic long fiber bundles whose ratio is 30 to 90%.
JP12710085A 1985-06-13 1985-06-13 Acrylic long fiber bundle having novel feeling and its production Granted JPS61289149A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12710085A JPS61289149A (en) 1985-06-13 1985-06-13 Acrylic long fiber bundle having novel feeling and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12710085A JPS61289149A (en) 1985-06-13 1985-06-13 Acrylic long fiber bundle having novel feeling and its production

Publications (2)

Publication Number Publication Date
JPS61289149A JPS61289149A (en) 1986-12-19
JPH036264B2 true JPH036264B2 (en) 1991-01-29

Family

ID=14951592

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12710085A Granted JPS61289149A (en) 1985-06-13 1985-06-13 Acrylic long fiber bundle having novel feeling and its production

Country Status (1)

Country Link
JP (1) JPS61289149A (en)

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5232229B2 (en) * 1971-10-04 1977-08-19
JPS5655248Y2 (en) * 1979-10-08 1981-12-23
JPS57101032A (en) * 1980-12-09 1982-06-23 Asahi Chemical Ind Acrylic flat bundle and method
JPS6010135B2 (en) * 1981-08-17 1985-03-15 旭化成株式会社 Manufacturing method of flat yarn
JPS61239031A (en) * 1985-04-09 1986-10-24 三菱レイヨン株式会社 Acrylic flat yarn and its production

Also Published As

Publication number Publication date
JPS61289149A (en) 1986-12-19

Similar Documents

Publication Publication Date Title
US4297412A (en) Two-component mixed acrylic fibres wherein acrylic components have different amounts of non-ionizable plasticizing comonomer
US2312152A (en) Rayon and method of manufacturing same
KR101206562B1 (en) Spun isotropic pitch-based carbon fiber yarn, composite yarn and woven fabric made by using the same, and processes for the production of them
US4140844A (en) Polyacrylonitrile filament yarns
WO1997013897A1 (en) False twisted yarn
TW202033850A (en) Precursor fiber bundle production method, carbon fiber bundle production method, and carbon fiber bundle
US3751547A (en) Process for producing high modulus polyvinyl alcohol synthetic fibers
US1989101A (en) Process for improving artificial fibers or fabrics
JPH036264B2 (en)
JPS6122046B2 (en)
JPS5950762B2 (en) Manufacturing method of flexible raw silk
JPS6115168B2 (en)
JP2017137602A (en) Manufacturing method of polyacrylonitrile fiber bundle
US2669766A (en) Crepe fabric
US2954270A (en) Process of producing a shrinkable cellulose textile filament
JPS6130042B2 (en)
JPS60119248A (en) Method for manufacturing textiles using mixed spun yarn using water-soluble polyvinyl alcohol long fibers
JP2004346447A (en) Method for producing acrylic fiber
JP7408406B2 (en) Method for manufacturing flame-resistant fiber bundle, method for manufacturing carbon fiber bundle, and connection device
JPH10158976A (en) Elongated animal hair fiber and method for producing the same
JPS5837411B2 (en) Carbon fiber manufacturing method
JPS63264918A (en) Production of carbon fiber
JPS6010135B2 (en) Manufacturing method of flat yarn
JPS6050883B2 (en) Novel acrylonitrile synthetic fiber and its manufacturing method
JPS6311466B2 (en)