JP2001172821A - Production of polyoxymethylene fiber - Google Patents

Production of polyoxymethylene fiber

Info

Publication number
JP2001172821A
JP2001172821A JP36272499A JP36272499A JP2001172821A JP 2001172821 A JP2001172821 A JP 2001172821A JP 36272499 A JP36272499 A JP 36272499A JP 36272499 A JP36272499 A JP 36272499A JP 2001172821 A JP2001172821 A JP 2001172821A
Authority
JP
Japan
Prior art keywords
polyoxymethylene
fiber
speed
yarn
producing
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
JP36272499A
Other languages
Japanese (ja)
Inventor
Koji Inagaki
孝司 稲垣
Tomonobu Nakamura
智信 中村
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.)
Unitika Ltd
Original Assignee
Unitika 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 Unitika Ltd filed Critical Unitika Ltd
Priority to JP36272499A priority Critical patent/JP2001172821A/en
Publication of JP2001172821A publication Critical patent/JP2001172821A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a method for producing an extremely strong fiber having heat resistance, abrasion resistance and chemical resistance inherent to a polyoxymethylene stably for a long time in high speed. SOLUTION: This method for producing a polyoxymethylene fiber is to melt extrude the polyoxymethylene in a condition satisfying a specific condition, draw the undrawn fiber in >=200 m/min speed, continuously draw the fiber in >=4 times and wind up the fiber in 1,200 m/min.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、高強度を有するポ
リオキシメチレン繊維を高速で、操業性よく製造する方
法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a high-strength polyoxymethylene fiber at high speed and with good operability.

【0002】[0002]

【従来の技術】ポリオキシメチレンは耐熱性、耐摩耗性
及び耐薬品性に優れたポリマーであり、ポリマー自体は
例えば特開平6-211953号公報に記載されているように公
知のポリマーであって、エンジニアリングプラスチック
として歯車等の成形品に多く用いられている。
2. Description of the Related Art Polyoxymethylene is a polymer having excellent heat resistance, abrasion resistance and chemical resistance. The polymer itself is a known polymer as described in, for example, JP-A-6-211953. It is widely used as an engineering plastic for molded products such as gears.

【0003】このポリオキシメチレンを繊維としたもの
も提案されており、ポリオキシメチレン繊維の製造方法
として、例えば、特公昭55-22566号公報には、特定温度
範囲で延伸および熱処理を行い弾性回復率の優れた繊維
を得る方法、特開昭60-52618号公報には、一度巻き取っ
た未延伸糸を低速で多段の延伸を行い、高強度高弾性率
繊維を得る方法、特開平8-113823号公報には、特定範囲
の溶融粘度のポリオキシメチレンを原料として溶融紡糸
する方法等が開示されている。
[0003] Polyoxymethylene fibers have also been proposed. As a method for producing polyoxymethylene fibers, for example, Japanese Patent Publication No. 55-22566 discloses an elastic recovery method in which stretching and heat treatment are performed in a specific temperature range. Japanese Patent Application Laid-Open No. 60-52618 discloses a method of obtaining a fiber having a high modulus of elasticity, a method of performing multi-stage drawing of an undrawn yarn once wound at low speed to obtain a high-strength high-modulus fiber, No. 113823 discloses a method of melt spinning using polyoxymethylene having a melt viscosity in a specific range as a raw material.

【0004】しかしながら、上述した特公昭55-22566号
公報の方法で得られた繊維は、引張強度が、非常に低い
ものであった。特開昭60-52618号公報の記載の方法で
は、一度巻き取った未延伸糸を低速で多段延伸を行うた
め、生産速度が遅いという問題がある。また、特開平8-
113823号公報の方法では、分子量が低いポリオキシメチ
レンを原料としているため、強度が4g/d程度であ
り、産業資材用に用いることは困難であった。
[0004] However, the fiber obtained by the method disclosed in Japanese Patent Publication No. 55-22566 has a very low tensile strength. The method described in Japanese Patent Application Laid-Open No. 60-52618 has a problem that the production speed is low because the undrawn yarn once wound is subjected to multi-stage drawing at a low speed. Also, JP-A-8-
In the method of JP-A-113823, since polyoxymethylene having a low molecular weight is used as a raw material, the strength is about 4 g / d, and it has been difficult to use it for industrial materials.

【0005】このように、高強度で産業資材分野に好適
に使用できるポリオキシメチレン繊維を、操業性よく得
る方法は提案されていなかった。
[0005] As described above, no method has been proposed for obtaining polyoxymethylene fibers having high strength and suitable for use in industrial materials with good operability.

【0006】[0006]

【発明が解決しようとする課題】本発明は、上記した問
題点を解決し、ポリオキシメチレンの特性である耐熱
性、耐摩耗性及び耐薬品性を具備した高強度繊維を、長
時間安定して高速で生産できる製造方法を提供すること
を技術的な課題とするものである。
SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems and provides a high-strength fiber having heat resistance, abrasion resistance and chemical resistance characteristic of polyoxymethylene for a long time. It is an object of the present invention to provide a manufacturing method that can be manufactured at high speed at high speed.

【0007】[0007]

【課題を解決するための手段】本発明者らは、上記課題
を達成するために、ポリオキシメチレン未延伸糸の延伸
におけるメカニズムを構造、物性の両面から鋭意検討の
結果、溶融押出しされた未延伸糸の状態と延伸条件がポ
リオキシメチレン繊維の物性を発現させる重要な要因で
あることを知見し、ポリオキシメチレンコポリマーを特
定条件で溶融押出しし、連続的に延伸を行い、未延伸糸
の状態と、延伸条件を良好にコントロールすることによ
り均一な延伸が行われ、高強度繊維を操業性よく得るこ
とができることを見出し、本発明に到達したものであ
る.
Means for Solving the Problems In order to achieve the above-mentioned object, the present inventors have conducted intensive studies on the mechanism of drawing a polyoxymethylene undrawn yarn from both the structure and physical properties. He discovered that the state of the drawn yarn and the drawing conditions were important factors for expressing the physical properties of the polyoxymethylene fiber, and melt-extruded the polyoxymethylene copolymer under specific conditions, and continuously drawn the undrawn yarn. The state and uniform stretching are performed by controlling the stretching conditions well, and it has been found that high-strength fibers can be obtained with good operability, and the present invention has been achieved.

【0008】すなわち、本発明は、ポリオキシメチレン
繊維を製造する方法において、オキシエチレン成分が
0.1〜10.0mol%共重合されたポリオキシメチ
レンを(1)式を満たす条件で溶融し、(2)式を満足する条
件で紡出させ、かつ紡糸した糸条を200m/分以上の
引取速度で引き取り、4.0倍以上に延伸し、1200
m/分以上の速度で捲き取ることを特徴とするポリオキ
シメチレン繊維の製造方法を要旨とするものである。 1800≦ T × t ≦4800 (1)式 T:溶融温度(℃) t:溶融時間(分) 50≦df≦500 (2)式 df = πρD2s /4q ρ:ポリマー溶融密度(g/cm3) D:ノズル孔径(mm) s:引取速度(m/分) q:単孔吐出量(g/
分)
That is, the present invention provides a method for producing a polyoxymethylene fiber, comprising melting a polyoxymethylene copolymerized with 0.1 to 10.0 mol% of an oxyethylene component under a condition satisfying the formula (1), The yarn spun and spun under the conditions satisfying the formula (2) is taken up at a take-up speed of 200 m / min or more and stretched 4.0 times or more.
A gist of the present invention is a method for producing polyoxymethylene fiber, which is characterized by winding at a speed of at least m / min. 1800 ≦ T × t ≦ 4800 (1) Equation T: Melting temperature (° C.) t: Melting time (minute) 50 ≦ df ≦ 500 (2) Equation df = πρD 2 s / 4q ρ: Polymer melt density (g / cm) 3 ) D: Nozzle hole diameter (mm) s: Take-off speed (m / min) q: Single hole discharge amount (g /
Minutes)

【0009】[0009]

【発明の実施の形態】以下、本発明について詳細に説明
する。本発明のポリオキシメチレン繊維を形成するポリ
オキシメチレンは、ホルムアルデヒドまたはトリオキサ
ンを出発物資としたポリマーで、共重合ポリマーとし
て、エチレンオキサイドを0.1〜10.0mol%共重合させた
ものである。共重合成分を含有させることによって、ホ
モポリマーに比較して熱安定性が改良され、また、溶融
ポリマー冷却過程で起こる結晶化の速度の低下が起こ
り、引き続き行う延伸を容易にさせ、分子鎖の配向によ
る高強度化が可能になるという効果がある。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. The polyoxymethylene that forms the polyoxymethylene fiber of the present invention is a polymer starting from formaldehyde or trioxane, and is obtained by copolymerizing 0.1 to 10.0 mol% of ethylene oxide as a copolymer. By including the copolymer component, the thermal stability is improved as compared with the homopolymer, and the rate of crystallization that occurs in the process of cooling the molten polymer is reduced. There is an effect that high strength can be achieved by orientation.

【0010】共重合成分が0.1mol%未満であると、上記
の効果を奏することができず、10.0mol%を超えると、ポ
リオキシメチレンの特性(耐熱性、耐摩耗性、耐薬品性
等)が損なわれる。
If the amount of the copolymer component is less than 0.1 mol%, the above effects cannot be exerted. If the amount exceeds 10.0 mol%, the characteristics (heat resistance, abrasion resistance, chemical resistance, etc.) of the polyoxymethylene are obtained. Is impaired.

【0011】なお、この共重合ポリマーには、その効果
を損なわない範囲で、種々の顔料、帯電防止剤、可塑剤
などの添加剤が含まれていてもよい。
The copolymer may contain additives such as various pigments, antistatic agents and plasticizers as long as the effects are not impaired.

【0012】次に、この共重合ポリマーを、1800≦ T
× t ≦4800(T:溶融温度(℃) t:供給から押し出さ
れるまでに溶融する時間(分))の条件を満たすように溶
融を行う。
Next, this copolymer is prepared by adding 1800 ≦ T
× t ≦ 4800 (T: melting temperature (° C.) t: melting time from supply to extrusion (minutes)).

【0013】T×tが1800未満であると、ポリマーを完全
に溶融させて押し出すことが困難となり、一方、T×tが
4800を超えると、ポリマーの熱分解や変性が引き起こる
場合があり、連続的に操業することが困難となり、得ら
れる繊維の物性も低下する。
When T × t is less than 1800, it is difficult to completely melt and extrude the polymer, while T × t is
If it exceeds 4800, thermal decomposition or modification of the polymer may occur, making it difficult to operate continuously, and the physical properties of the obtained fiber also deteriorate.

【0014】そして、紡糸する条件、ノズルから上記の
条件で溶融したポリマーを吐出させる条件として、50
≦df≦500を満足する必要がある。df = πρD2
s /4qであり、ポリマー溶融密度(ρ:g/cm3)、
ノズル孔径(D:mm)、引取速度(s:m/分)、単孔吐
出量(q:g/分)との関係を表わすもので、ノズル孔
から押し出された溶融ポリマーが冷却固化するまでの変
形の指標となるものである。ここにおいて、ポリマー溶
融密度とは、溶融を行う温度において規定体積およびそ
の時の重量を測定し、換算するものである。
The spinning conditions and the conditions for discharging the polymer melted under the above conditions from the nozzle are as follows.
≦ df ≦ 500. df = πρD 2
s / 4q, the polymer melt density (ρ: g / cm 3 ),
The relationship between nozzle hole diameter (D: mm), take-off speed (s: m / min), and single-hole discharge amount (q: g / min). Until the molten polymer extruded from the nozzle hole solidifies by cooling. Is an index of the deformation of. Here, the polymer melt density is a value obtained by measuring and converting a specified volume and a weight at a temperature at which melting is performed.

【0015】dfが50未満であると、均一な糸条の引取
りが困難となり、500を超えると、引き取り時の変形が
大きくなる結果、糸切れを起こしたり、均一な糸条が得
られない等の問題を引き起こす。
If the df is less than 50, it is difficult to take out a uniform yarn. If the df is more than 500, the deformation at the time of the take-up becomes large, resulting in thread breakage and uniform yarn cannot be obtained. Etc. cause problems.

【0016】紡糸した糸条は、冷却し、必要であれば油
剤を付与する。そして、上記のdfを規定する因子であ
る糸条の引取速度は、200m/分以上であることが必
要である。200m/分未満であると糸速が遅いため、
均一な糸質のものを得ることが困難となる。さらに、生
産性も悪く、コスト的に不利である。
The spun yarn is cooled and, if necessary, an oil agent is applied. The yarn take-off speed, which is a factor defining the above df, needs to be 200 m / min or more. If the speed is less than 200 m / min, the yarn speed is low.
It is difficult to obtain a uniform yarn quality. Further, the productivity is low and the cost is disadvantageous.

【0017】さらに、溶融紡出した未延伸糸は引取ロー
ラを経た後、連続して延伸することが必要である。本発
明では、紡出した糸条を完全に冷却する以前に延伸処理
を施すことが有効であり、糸条温度は室温以上、好まし
くは、30℃以上であることが好ましい。糸条が完全に冷
却されると、結晶化が進行し、延伸処理が困難となる場
合があるためである。
Further, it is necessary to continuously stretch the undrawn yarn melt-spun after passing through a take-up roller. In the present invention, it is effective to carry out a drawing treatment before completely cooling the spun yarn, and the yarn temperature is preferably room temperature or higher, preferably 30 ° C. or higher. This is because, when the yarn is completely cooled, crystallization proceeds, and the drawing treatment may be difficult.

【0018】延伸処理の延伸倍率は4倍以上であること
が必要である。4倍未満であると分子鎖の配向が十分に進
まず、高強度の繊維を得ることが困難となる。具体的な
延伸方法としては、複数のローラ間で多段延伸し、この
とき、糸条を加熱する手段として、加熱ローラとした
り、ローラ間にヒータを設けて延伸することが好まし
い。
The stretching ratio in the stretching process must be 4 times or more. If the ratio is less than 4 times, the orientation of the molecular chains does not proceed sufficiently, and it is difficult to obtain high-strength fibers. As a specific stretching method, it is preferable that the stretching is performed in a multi-stage manner between a plurality of rollers, and at this time, the yarn is heated by using a heating roller or a heater is provided between the rollers.

【0019】そして、延伸処理を施した糸条は、120
0m/分以上の速度で捲き取ることが好ましい。120
0m/分未満では、延伸倍率が4倍未満となり、延伸で
の配向が十分に進まず、高強度繊維が得られない。そし
て、操業性を向上させるために、さらには、2000m/分
以上の巻取速度とすることが好ましい。
The stretched yarn is 120
It is preferable to wind up at a speed of 0 m / min or more. 120
If it is less than 0 m / min, the draw ratio will be less than 4 times, the orientation during stretching will not proceed sufficiently, and a high-strength fiber will not be obtained. Then, in order to improve the operability, it is preferable to set the winding speed to 2000 m / min or more.

【0020】[0020]

【実施例】以下、実施例により本発明を具体例に説明す
る。なお、実施例における各物性値は、下記の方法で測
定したものである。 a)ポリマー溶融密度 前記の方法で測定した。 b)強度 島津製作所製オートグラフDSS-500型を用いて、試料長3
0cm、つかみ間隔5cm、引張速度30cm/minの条件で測定し
た平均値を繊維の強度とした。 c)製糸性の良否 連続して24時間紡糸を行い、その間の糸切れ、ローラへ
の単糸捲き等の状況により次の二段階で評価した。 ○:良好 ×:不良
The present invention will be described below in more detail with reference to examples. In addition, each physical property value in an Example is measured by the following method. a) Polymer melt density Measured by the method described above. b) Strength Using a Shimadzu Autograph DSS-500, sample length 3
The average value measured under the conditions of 0 cm, a grip interval of 5 cm, and a tensile speed of 30 cm / min was defined as the fiber strength. c) Quality of yarn-making properties Continuous spinning was performed for 24 hours, and the evaluation was made in the following two stages according to the conditions such as yarn breakage and winding of a single yarn to a roller during the spinning. :: good ×: bad

【0021】実施例1 エチレンオキサイドが1.6mol%共重合されたポリオキシ
メチレンコポリマーのチップをエクストルーダに供給
し、エクストルーダ内で220℃で10分間溶融を行い、溶
融密度1.2の溶融ポリマーを、直径0.5mmの孔を48個有す
る紡糸口金から、単孔吐出量1.1g/分で押出し、空気中
で冷却後、油剤を付与して500m/分の速度で引き取っ
た。引き続いてその糸条を、まず150℃の加熱ローラで
5.0倍に延伸し、更に、180℃の加熱ローラで1.2倍の延
伸を施し、全延伸倍率を6.0倍とし、3000m/分の
速度で巻き取った。得られた繊維の物性、製糸性の評価
を表1に示す。
Example 1 A chip of a polyoxymethylene copolymer in which ethylene oxide was copolymerized at 1.6 mol% was supplied to an extruder, and melted at 220 ° C. for 10 minutes in the extruder. It was extruded from a spinneret having 48 mm holes at a single hole discharge rate of 1.1 g / min, cooled in air, applied with an oil agent, and taken off at a speed of 500 m / min. Subsequently, the yarn is first heated with a 150 ° C heating roller.
The film was stretched 5.0 times, and further stretched 1.2 times with a heating roller at 180 ° C. to make the total stretch ratio 6.0 times and wound at a speed of 3000 m / min. Table 1 shows the evaluation of the physical properties and the spinning properties of the obtained fibers.

【0022】実施例2〜3、比較例1〜3 表1に示すように溶融、紡糸時の各種の値、延伸倍率、
巻取速度を変更した以外は、実施例1と同様にして行っ
た。得られた繊維の物性、製糸性の評価を表1に示す。
Examples 2-3, Comparative Examples 1-3 As shown in Table 1, various values at the time of melting and spinning, stretching ratio,
The procedure was performed in the same manner as in Example 1 except that the winding speed was changed. Table 1 shows the evaluation of the physical properties and the spinning properties of the obtained fibers.

【0023】[0023]

【表1】 【table 1】

【0024】表1から明らかなように、実施例1〜3で
は、製糸性よく高強度のポリオキシメチレン繊維を得る
ことができた。一方、比較例1は、溶融時間の値が大き
すぎ、T×tが4800を超え、ポリマーが熱劣化し、糸切
れが多発して繊維を得ることができなかった。比較例2
は、dfが500を超えたため、引き取り時の変形が大
きくなり、糸切れが多発し、延伸を行うことができなか
った。比較例3は、延伸倍率が4倍未満であったため、
得られた繊維は強度の低いものであった。
As is clear from Table 1, in Examples 1 to 3, high strength polyoxymethylene fibers were obtained with good spinning properties. On the other hand, in Comparative Example 1, the value of the melting time was too large, Txt exceeded 4,800, the polymer was thermally degraded, and yarn breakage occurred frequently, and fibers could not be obtained. Comparative Example 2
Since df exceeded 500, deformation at the time of take-up became large, thread breakage occurred frequently, and stretching could not be performed. In Comparative Example 3, since the stretching ratio was less than 4 times,
The obtained fiber had low strength.

【0025】[0025]

【発明の効果】本発明のポリオキシメチレン繊維の製造
方法によれば、高強度で各種の産業資材用途にも十分に
使用できるポリオキシメチレン繊維を、ナイロン・ポリ
エステルなどの合成繊維と同様に高速で安定して得るこ
とが可能になる。
According to the method for producing polyoxymethylene fiber of the present invention, polyoxymethylene fiber which is high in strength and can be sufficiently used for various industrial materials can be produced at high speed similarly to synthetic fibers such as nylon and polyester. And it can be obtained stably.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ポリオキシメチレン繊維を製造する方法
において、オキシエチレン成分が0.1〜10.0mo
l%共重合されたポリオキシメチレンを(1)式を満たす
条件で溶融し、(2)式を満足する条件で紡出させ、かつ
紡糸した糸条を200m/分以上の引取速度で引き取
り、4.0倍以上に延伸し、1200m/分以上の速度
で捲き取ることを特徴とするポリオキシメチレン繊維の
製造方法。 1800≦ T × t ≦4800 (1)式 T:溶融温度(℃) t:溶融時間(分) 50≦df≦500 (2)式 df = πρD2s /4q ρ:ポリマー溶融密度(g/cm3) D:ノズル孔径(mm) s:引取速度(m/分) q:単孔吐出量(g/
分)
1. A method for producing a polyoxymethylene fiber, wherein the oxyethylene component is 0.1 to 10.0 mol.
1% of the copolymerized polyoxymethylene is melted under the condition satisfying the formula (1), spun under the condition satisfying the formula (2), and the spun yarn is taken off at a take-up speed of 200 m / min or more, A method for producing a polyoxymethylene fiber, comprising drawing the film to 4.0 times or more and winding it up at a speed of 1200 m / min or more. 1800 ≦ T × t ≦ 4800 (1) Equation T: Melting temperature (° C.) t: Melting time (minute) 50 ≦ df ≦ 500 (2) Equation df = πρD 2 s / 4q ρ: Polymer melt density (g / cm) 3 ) D: Nozzle hole diameter (mm) s: Take-off speed (m / min) q: Single hole discharge amount (g /
Minutes)
JP36272499A 1999-12-21 1999-12-21 Production of polyoxymethylene fiber Pending JP2001172821A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP36272499A JP2001172821A (en) 1999-12-21 1999-12-21 Production of polyoxymethylene fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP36272499A JP2001172821A (en) 1999-12-21 1999-12-21 Production of polyoxymethylene fiber

Publications (1)

Publication Number Publication Date
JP2001172821A true JP2001172821A (en) 2001-06-26

Family

ID=18477582

Family Applications (1)

Application Number Title Priority Date Filing Date
JP36272499A Pending JP2001172821A (en) 1999-12-21 1999-12-21 Production of polyoxymethylene fiber

Country Status (1)

Country Link
JP (1) JP2001172821A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003025268A1 (en) * 2001-09-18 2003-03-27 Polyplastics Co., Ltd. Polyoxymethylene fiber and method for production thereof
JP2006009205A (en) * 2004-06-28 2006-01-12 Polyplastics Co Conjugate fiber made of polyoxymethylene resin
US7410696B2 (en) 2005-01-12 2008-08-12 Ticona Gmbh Polyoxymethylene fibers, production thereof and use thereof
WO2010001558A1 (en) * 2008-07-02 2010-01-07 三菱瓦斯化学株式会社 Low-fisheye polyacetal resin
JPWO2014050448A1 (en) * 2012-09-26 2016-08-22 三菱瓦斯化学株式会社 Polyacetal drawn fiber
CN106521704A (en) * 2016-10-31 2017-03-22 江苏苏博特新材料股份有限公司 Polyketone-polyformaldehyde composite fiber preparation method
CN107938019A (en) * 2017-10-16 2018-04-20 唐山开滦化工科技有限公司 A kind of one-step shaping preparation method of polyformaldehyde fibre
WO2019012876A1 (en) 2017-07-14 2019-01-17 三菱瓦斯化学株式会社 Method for producing polyacetal fiber
WO2019012877A1 (en) 2017-07-14 2019-01-17 三菱瓦斯化学株式会社 Method for manufacturing polyacetal fiber

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003025268A1 (en) * 2001-09-18 2003-03-27 Polyplastics Co., Ltd. Polyoxymethylene fiber and method for production thereof
JP2003089925A (en) * 2001-09-18 2003-03-28 Polyplastics Co Polyoxymethylene fiber and method for producing the same
US6818294B2 (en) 2001-09-18 2004-11-16 Polyplastics Co., Ltd. Polyoxymethylene fiber and method for production thereof
CN100334271C (en) * 2001-09-18 2007-08-29 宝理塑料株式会社 Polyoxymethylene fiber and method for production thereof
JP2006009205A (en) * 2004-06-28 2006-01-12 Polyplastics Co Conjugate fiber made of polyoxymethylene resin
KR101184857B1 (en) * 2004-06-28 2012-09-20 폴리플라스틱스 가부시키가이샤 A composite fiber made of polyoxy methylene resins
US7410696B2 (en) 2005-01-12 2008-08-12 Ticona Gmbh Polyoxymethylene fibers, production thereof and use thereof
WO2010001558A1 (en) * 2008-07-02 2010-01-07 三菱瓦斯化学株式会社 Low-fisheye polyacetal resin
JP5648477B2 (en) * 2008-07-02 2015-01-07 三菱瓦斯化学株式会社 Low fisheye polyacetal resin
US10253160B2 (en) 2012-09-26 2019-04-09 Mitsubishi Gas Chemical Company, Inc. Polyacetal stretched fiber
JPWO2014050448A1 (en) * 2012-09-26 2016-08-22 三菱瓦斯化学株式会社 Polyacetal drawn fiber
CN106521704A (en) * 2016-10-31 2017-03-22 江苏苏博特新材料股份有限公司 Polyketone-polyformaldehyde composite fiber preparation method
CN106521704B (en) * 2016-10-31 2019-03-08 江苏苏博特新材料股份有限公司 A kind of preparation method of polyketone-polyformaldehyde composite fibre
WO2019012876A1 (en) 2017-07-14 2019-01-17 三菱瓦斯化学株式会社 Method for producing polyacetal fiber
WO2019012877A1 (en) 2017-07-14 2019-01-17 三菱瓦斯化学株式会社 Method for manufacturing polyacetal fiber
KR20200029512A (en) 2017-07-14 2020-03-18 미츠비시 가스 가가쿠 가부시키가이샤 Manufacturing method of polyacetal fiber
KR20200032120A (en) 2017-07-14 2020-03-25 미츠비시 가스 가가쿠 가부시키가이샤 Manufacturing method of polyacetal fiber
US11441242B2 (en) 2017-07-14 2022-09-13 Mitsubishi Gas Chemical Company, Inc. Method for manufacturing polyacetal fiber
US11761121B2 (en) 2017-07-14 2023-09-19 Mitsubishi Gas Chemical Company, Inc. Method for producing polyacetal fiber
KR20230174292A (en) 2017-07-14 2023-12-27 미츠비시 가스 가가쿠 가부시키가이샤 Method for producing polyacetal fiber
CN107938019A (en) * 2017-10-16 2018-04-20 唐山开滦化工科技有限公司 A kind of one-step shaping preparation method of polyformaldehyde fibre
CN107938019B (en) * 2017-10-16 2020-04-07 唐山开滦化工科技有限公司 One-step forming preparation method of polyformaldehyde fibers

Similar Documents

Publication Publication Date Title
US4911165A (en) Pliabilized polypropylene surgical filaments
US9057148B2 (en) High-strength polypropylene fiber and method for producing the same
JP2001172821A (en) Production of polyoxymethylene fiber
WO2002064867A1 (en) Resin compositions, monofilaments, process for producing the same and fishng lines
JP4337539B2 (en) Polyester fiber production method and spinneret for melt spinning
US5006296A (en) Process for the preparation of fibers of stereoregular polystyrene
JPH09241924A (en) Drawn polyamide fiber and its production
JPH039204B2 (en)
JP7275733B2 (en) High strength polyamide monofilament
JP2000154425A (en) Production of biodegradable monofilament
JP3462977B2 (en) Method for producing polylactic acid fiber
JPS61124622A (en) Monofilament of nylon 46
JP3161546B2 (en) Method for producing high strength, low shrinkage polyester fiber
JP2002146637A (en) Method for producing polyoxymethylene fiber
WO2023074268A1 (en) High-strength, high-elongation polypropylene fiber and production method thereof
EP4190953A1 (en) Polyethylene yarn having improved post-processability, and fabric comprising same
JPH04343710A (en) Production of aromatic polyetherketone monofilament
JP2000345428A (en) Production of polyolefin-based fiber
WO1999029935A1 (en) Method of producing synthetic fiber and the synthetic fiber
JPS61174416A (en) Drawn yarn of ultra-high-molecular-weight polyethylene, method for producing raw yarn thereof, and apparatus therefor
JP2023051860A (en) Polyether sulfone fiber, fiber package, nonwoven fabric, and manufacturing method of polyether sulfone fiber
JPH03294517A (en) Aromatic polyester fiber having high strength and high modulus of elasticity
JPH1181036A (en) High strength polypropylene fiber and its production
JP2006336117A (en) Method for producing polyester hollow yarn
JPS6141318A (en) Manufacture of multifilament