JPS63317032A - Fishing line - Google Patents

Fishing line

Info

Publication number
JPS63317032A
JPS63317032A JP15276587A JP15276587A JPS63317032A JP S63317032 A JPS63317032 A JP S63317032A JP 15276587 A JP15276587 A JP 15276587A JP 15276587 A JP15276587 A JP 15276587A JP S63317032 A JPS63317032 A JP S63317032A
Authority
JP
Japan
Prior art keywords
aromatic
fishing line
aromatic polyester
acid
yarn
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.)
Granted
Application number
JP15276587A
Other languages
Japanese (ja)
Other versions
JP2522947B2 (en
Inventor
Toshiyuki Kobashi
小橋 利行
Seiji Takao
高尾 精二
Jun Takagi
潤 高木
Hiroaki Sugimoto
杉本 宏明
Kazuo Hayatsu
早津 一雄
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.)
Japan Exlan Co Ltd
Sumitomo Chemical Co Ltd
Original Assignee
Japan Exlan Co Ltd
Sumitomo Chemical 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 Japan Exlan Co Ltd, Sumitomo Chemical Co Ltd filed Critical Japan Exlan Co Ltd
Priority to JP62152765A priority Critical patent/JP2522947B2/en
Publication of JPS63317032A publication Critical patent/JPS63317032A/en
Application granted granted Critical
Publication of JP2522947B2 publication Critical patent/JP2522947B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a fishing line capable of thinning, having excellent rigidity, sinking speed and durability, slightly causing backlash and entanglement, comprising an aromatic polyester yarn having tensile breaking strength and density adjusted to >=specific values. CONSTITUTION:For example, 40-70mol.% p-hydroxybenzoic acid, 15-30mol.% aromatic dicarboxylic acid such as terephthalic acid and 15-30mol.% aromatic diol such as resorcinol are subjected to polycondensation by esterifying or ester interchange reaction at 150-360 deg.C at normal pressure or under reduced pressure at 10-0.1Torr to give an aromatic polyester showing anisotropy in melting. The polyester is subjected to melt spinning at 280-420 deg.C to give aromatic polyester yarn having >=100kg/mm<2> tensile breaking strength and >=1.38g/cc density. Then the yarn is processed into a fishing line.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は釣糸に関する。[Detailed description of the invention] <Industrial application field> FIELD OF THE INVENTION The present invention relates to fishing lines.

〈従来の技術と問題点〉 従来釣糸には、ポリアミド、ポリエステル等の有機繊維
の延伸系が使用されてきた。
<Prior Art and Problems> Conventionally, fishing lines have been made of drawn organic fibers such as polyamide and polyester.

しかしこれらの素材からの釣糸は一般に強度が充分でな
いため、太い直径のものを用いざるをえず、潮流の影響
を受けやすいとか、魚に警戒心を与えるため魚のエサへ
の食いつきが悪いとか、釣糸の伸度が大きいため、魚が
掛かったことを示す魚信が減衰されやすく手元や竿先ま
で伝達されにくいとか、弾性率が低いため腰がなく糸同
士の絡まりやもつれを起こしやすいとか、吸水性が大き
いため取扱や寿命に難があるとか、太く密度が小さいた
め、投げ釣りゃ深海的りにおいて釣糸の沈み速度が遅い
等の問題を抱えている。
However, fishing lines made from these materials are generally not strong enough, so they have to use ones with a large diameter, which means they are easily affected by currents, and they tend to make fish wary, making them less likely to bite into the bait. Because the fishing line has a high elongation, the fish signal indicating that a fish has been hooked is easily attenuated and is difficult to transmit to the hand or the tip of the rod.The elastic modulus is low, so the line has no elasticity and is prone to entanglement and tangles among the lines. Due to its high water absorption, it is difficult to handle and have a long lifespan, and because it is thick and has low density, it has problems such as slow sinking speed of the fishing line when fishing in deep sea.

これらを改良するために、釣糸表面に防水加工を施すと
か、多FJ!織構造とする等の工夫がなされているが、
未だ充分とはいえない。
In order to improve these problems, waterproofing is applied to the surface of the fishing line. Although efforts have been made to create a woven structure,
It's still not enough.

高強度のポリエチレン繊維も開発されつつあるが密度が
水より小さく、アラミド繊維は吸水性であるため、上述
の問題の解決にはならない。また金属繊維、ガラス繊維
、炭素繊維等の繊維は取扱が難しい。
High-strength polyethylene fibers are also being developed, but they do not solve the above problems because their density is lower than that of water, and aramid fibers are water-absorbing. Furthermore, fibers such as metal fibers, glass fibers, and carbon fibers are difficult to handle.

このため軽量で高強度、高弾性率を存し、腰のある釣糸
が望まれている。
For this reason, a fishing line that is lightweight, has high strength, high elastic modulus, and has stiffness is desired.

本発明の目的は、かがる問題点を改善した釣糸を提供す
ることにある。
An object of the present invention is to provide a fishing line that has improved the problem of darning.

〈問題点を解決するための手段〉 本発明は、引っ張り破断強度カ月00kg/mm2以上
、密度1.38g、/cc以上の芳香族ポリエステル繊
維からなる釣糸に関するものである。
<Means for Solving the Problems> The present invention relates to a fishing line made of aromatic polyester fiber having a tensile strength at break of 00 kg/mm 2 or more per month and a density of 1.38 g/cc or more.

本発明における芳香族ポリエステル繊維とは、例えば特
公昭55−20008号、特開昭58−191219号
公報等に示される方法によって得ることができる。
The aromatic polyester fiber in the present invention can be obtained, for example, by the method disclosed in Japanese Patent Publication No. 55-20008, Japanese Patent Application Laid-open No. 58-191219, and the like.

好ましい芳香族ポリエステル繊維は溶融時に異方性を示
す芳香族ポリエステルから溶融紡糸によって得られる繊
維である。中でも弾性率が67on/ am ”以上、
伸度が10%以下のものが、腰があり、絡まりやもつれ
がなく、魚信が鋭敏に伝達される等の点で好ましい。
Preferred aromatic polyester fibers are fibers obtained by melt spinning from aromatic polyesters that exhibit anisotropy when melted. Among them, the elastic modulus is 67 on/am” or more,
A material with an elongation of 10% or less is preferable because it has firmness, does not get tangled or tangled, and allows for sharp transmission of fish movements.

)8融時に異方性を示す芳香族ポリエステルは、芳香族
ジカルボン酸と芳香族ジオール及び/又は芳香族ヒドロ
キシカルボン酸やこれらの誘導体から形成されるもので
、場合によりこれらと脂環族ジオール、脂肪族ジオール
やこれらの誘導体との共重合体も含まれる。
) 8 Aromatic polyesters exhibiting anisotropy when melted are formed from aromatic dicarboxylic acids, aromatic diols and/or aromatic hydroxycarboxylic acids, and derivatives thereof, and in some cases, these and alicyclic diols, Copolymers with aliphatic diols and derivatives thereof are also included.

ここで芳香族ジカルボン酸としてはテレフタル酸、イソ
フタル酸、4,4°−ジカルボキシジフェニル、2.6
−ジカルボキシナフタレン、1.2−ビス(4−カルボ
キシフェノキシ)エタン等やこれらのアルキル、アリー
ル、アルコキシ、ハロゲン基の核置換体が挙げられる。
Here, the aromatic dicarboxylic acids include terephthalic acid, isophthalic acid, 4,4°-dicarboxydiphenyl, 2.6
-dicarboxynaphthalene, 1,2-bis(4-carboxyphenoxy)ethane, etc., and their alkyl, aryl, alkoxy, and halogen group-substituted products.

芳香族ジオールとしてはヒドロキノン、レゾルシン、4
.4’ −ジヒドロキシナフタレン、4.4° −ジヒ
ドロキシベンゾフヱノン、4.4′−ジヒドロキシジフ
ェニルエタン、4.4°−ジヒドロキシジフェニルエー
テル、4.4°−ジヒドロキシジフェニルスルフィド、
2.6−ジヒドロキシナフタレン、1.5−ジヒドロキ
シナフタレン、1.4−ジヒドロキシナフタレン、2.
2’−ビス(4−ヒドロキシフェニル)プロパン等やこ
れらのアルキル、アリール、アルコキシ、ハロゲン基の
核置換体が挙げられる芳香族ヒドロキシカルボン酸とし
てはp−ヒドロキシ安息香酸、m−ヒドロキシ安息香酸
、2−ヒドロキシナフタレン−6−カルボン酸、1−ヒ
ドロキシナフタレン−5−カルボン酸、p−4=ヒドロ
キシフエニル安息香酸等やこれらのアルキル、アリール
、アルコキシ、ハロゲン基の核置換体が挙げられる。
Aromatic diols include hydroquinone, resorcinol, 4
.. 4′-dihydroxynaphthalene, 4.4°-dihydroxybenzophenone, 4.4′-dihydroxydiphenylethane, 4.4°-dihydroxydiphenyl ether, 4.4°-dihydroxydiphenyl sulfide,
2.6-dihydroxynaphthalene, 1.5-dihydroxynaphthalene, 1.4-dihydroxynaphthalene, 2.
Examples of the aromatic hydroxycarboxylic acids include 2'-bis(4-hydroxyphenyl)propane, etc., and derivatives of these with alkyl, aryl, alkoxy, and halogen groups substituted with p-hydroxybenzoic acid, m-hydroxybenzoic acid, and 2'-bis(4-hydroxyphenyl)propane. Examples include -hydroxynaphthalene-6-carboxylic acid, 1-hydroxynaphthalene-5-carboxylic acid, p-4=hydroxyphenylbenzoic acid, and their alkyl, aryl, alkoxy, and halogen group-substituted products.

脂環族ジカルボン酸としてはtrans −1、4−ジ
カルボキシシクロヘキサン、cts−1,4−ジカルボ
キシシクロヘキサン等やこれらのアルキル、アリール、
アルコキシ、ハロゲン基の核置換体が挙げられる。
Examples of alicyclic dicarboxylic acids include trans-1,4-dicarboxycyclohexane, cts-1,4-dicarboxycyclohexane, and alkyl, aryl,
Nuclear substitution products of alkoxy and halogen groups can be mentioned.

脂環族及び脂肪族ジオールとしてはキシリレンジオール
、エチレングリコール、trans   1.4−ジヒ
ドロキシシクロヘキサン、cis−1,4−ジヒドロキ
シシクロヘキサン等やこれらのアルキル、アリール、ア
ルコキシ、ハロゲン基の核置換体が挙げられる。
Examples of alicyclic and aliphatic diols include xylylene diol, ethylene glycol, trans 1,4-dihydroxycyclohexane, cis-1,4-dihydroxycyclohexane, and their alkyl, aryl, alkoxy, and halogen group substituted products. It will be done.

本発明に用いられる芳香族ポリエステルは上記原料また
はそれらの誘導体の組合せ等をエステル化もしくはエス
テル交換反応により重縮合させることにより得られるが
、本発明の対象として好ましい芳香族ポリエステルとし
ては、例えば(1)p−ヒドロキシ安息香酸残基40〜
70モル%と上記芳香族ジカルボン酸残基15〜30モ
ル%と芳香族ジオール残基15〜30モル%からなるコ
ポリエステル、 (2)テレフタル酸及び/又はイソフタル酸とクロルヒ
ドロキノン、フェニルヒドロキノン及び/又はヒドロキ
ノンからなるコポリエステル、(3)p−ヒドロキシ安
息香酸残基20〜80モル%と2−ヒドロキシナフタレ
ン−6−カルボン酸残基20〜80モル%からなるコポ
リエステル等が挙げられる。
The aromatic polyester used in the present invention can be obtained by polycondensing the above-mentioned raw materials or combinations of their derivatives by esterification or transesterification reaction. ) p-hydroxybenzoic acid residue 40~
A copolyester consisting of 70 mol%, 15 to 30 mol% of the above aromatic dicarboxylic acid residues, and 15 to 30 mol% of aromatic diol residues, (2) terephthalic acid and/or isophthalic acid, chlorohydroquinone, phenylhydroquinone, and/or Alternatively, copolyesters consisting of hydroquinone, (3) copolyesters consisting of 20 to 80 mol% of p-hydroxybenzoic acid residues and 20 to 80 mol% of 2-hydroxynaphthalene-6-carboxylic acid residues, and the like.

重縮合反応としては既知の塊状重合、溶液重合、懸濁重
合法等を採用することができ、150〜360°Cで常
圧又は10〜O,1torrの減圧下に場合によりSb
、Ti、Ge化合物等の重合触媒、リン系化合物等の安
定剤、T i Ox、Ca COs、タルク等の充填剤
等を添加して行うことができる。
As the polycondensation reaction, known bulk polymerization, solution polymerization, suspension polymerization, etc. can be adopted, and in some cases, Sb is
, a polymerization catalyst such as a Ti or Ge compound, a stabilizer such as a phosphorous compound, a filler such as T i Ox, Ca COs, talc, etc. can be added.

得られたポリマーはそのままで、あるいは粉体状で不活
性気体中、又は減圧下に熱処理して紡糸用の試料として
もよいし、あるいは一度押出機により造粒して用いるこ
ともできる。
The obtained polymer may be used as it is, or may be heat-treated in powder form in an inert gas or under reduced pressure to be used as a sample for spinning, or it may be used after being granulated using an extruder.

溶融紡糸装置としては、加熱制御機構を備えたプランジ
ャー、スクリュー等の溶融部、ギャボンプ等の計量部、
紡糸口金を含む紡糸頭部を備えていればどのようなもの
でも使用できる。
The melt spinning equipment includes a plunger with a heating control mechanism, a melting part such as a screw, a measuring part such as a gabump,
Any spinning head including a spinneret can be used.

紡糸に適した温度は、280〜420°Cで、好ましく
は300〜400°Cである。280°Cより低いと装
置への負荷が大きくなったり、試料の溶融体の均一性が
充分でなかったり、逆に高温であると分解が起こったり
して、安定な紡糸を行うことができない。
The temperature suitable for spinning is 280-420°C, preferably 300-400°C. If the temperature is lower than 280°C, the load on the apparatus will be large, the uniformity of the sample melt will be insufficient, and if the temperature is high, decomposition may occur, making it impossible to perform stable spinning.

紡糸に用いる口金としては、一般に用いられている物を
そのまま使うこともできるが、好ましい紡糸口金として
は孔径(d)が0.15m以下で、且つ孔長(2)と孔
径との比<1/d)が0゜8以上の物が好ましい。
As the spinneret used for spinning, commonly used spinnerets can be used as they are, but preferred spinnerets have a hole diameter (d) of 0.15 m or less and a ratio of hole length (2) to hole diameter <1. /d) is preferably 0°8 or more.

得られた繊維はそのままでも使用できるが、延伸、熱処
理あるいはこれらを組み合わせた操作を施した後、用い
ても良い。
The obtained fibers can be used as they are, but they may also be used after being subjected to stretching, heat treatment, or a combination of these operations.

こうして得られた繊維は高強度、高弾性率、低伸度、低
吸水性であるが、腰が大きすぎる場合には、曲げに対す
る全反発力の調整のために太い直径のモノフィラメント
ではなく、細い直径の複数のフィラメントで撚り、編み
、織り等の加工をして用いることもできる。
The fiber thus obtained has high strength, high modulus, low elongation and low water absorption, but if the waist is too large, use a thin rather than a thick diameter monofilament for adjustment of the total rebound force against bending. It can also be used by twisting, knitting, or weaving filaments with multiple diameters.

〈発明の効果〉 本発明に用いる繊維は強度が高いので、必要な強力の釣
糸にするのに糸径を細くでき、弾性率が高いため腰があ
り絡まりやもつれが少なく、同時に水との馴染みが少な
く水より密度が大きいため水中に沈みやすく、吸水性で
ないため重みもなく保守も容易である。更に、低伸度、
高弾性率であるため、わずかの魚信が鋭敏に手元、竿先
に伝達される。また透明糸であることも利用しうる。
<Effects of the Invention> Since the fibers used in the present invention have high strength, the thread diameter can be made thinner to make the necessary strong fishing line, and the high elastic modulus makes it stiff and less likely to get tangled or tangled, while at the same time it has good compatibility with water. Because it has less water and is denser than water, it sinks easily in water, and because it is not absorbent, it is not heavy and easy to maintain. Furthermore, low elongation,
Due to its high elastic modulus, even the slightest fish signal is sensitively transmitted to the hand and the tip of the rod. Also, the fact that it is a transparent thread can be utilized.

〈実施例〉 以下に本発明の理解を容易にするため実施例を示すが、
これらばあ(まで例示的なものであり、本発明の要旨は
これらにより限定されるものではない。
<Examples> Examples are shown below to facilitate understanding of the present invention, but
These examples are merely illustrative, and the gist of the present invention is not limited thereto.

なお例中の特定値は、下記のごとくして測定算出したも
のである。
Note that the specific values in the examples were measured and calculated as follows.

(1)溶融時の光学異方性 ポリマー粉末を加熱ステージ上に置き、偏光下、25°
C/分で昇温し、肉眼観察で行った。
(1) Place the optically anisotropic polymer powder when melted on a heating stage, and hold it at 25° under polarized light.
The temperature was raised at a rate of C/min, and observation was made with the naked eye.

(2)繊維の引っ張り試験 東洋ボールドウィン製テンシロン■型引っ張り試験機を
用い、チャック間距#20閣、引っ張り速度2m/分で
測定した。試料数は24本で、最高及び最低値を除いた
値の平均値で示した。
(2) Fiber tensile test Measurement was carried out using a tensilon type tensile tester manufactured by Toyo Baldwin at a chuck distance of #20 and a tensile speed of 2 m/min. The number of samples was 24, and the average value excluding the highest and lowest values was shown.

参考例 p−アセトキシ安息香酸7.2kg(40モル)、テレ
フタル酸2.49kg(15モル)、イソフタル酸0.
83kg(5モル)、4.4’ −ジアセトキシジフェ
ニル5.45kg(20,2モル)を櫛型撹拌翼をもつ
重合槽に仕込み、窒素ガス雰囲気下で撹拌しながら昇温
し、330″Cで3時間重合した。
Reference example p-acetoxybenzoic acid 7.2 kg (40 mol), terephthalic acid 2.49 kg (15 mol), isophthalic acid 0.
83 kg (5 mol) and 5.45 kg (20.2 mol) of 4.4'-diacetoxydiphenyl were charged into a polymerization tank with comb-shaped stirring blades, heated to 330''C while stirring under nitrogen gas atmosphere. Polymerization was carried out for 3 hours.

この間生成する酢酸を除去し、強力な撹拌で重合を行い
、冷却後ポリマーを取り出したところ、収量は10.8
8kgで理論収量の97.8%であった。
The acetic acid produced during this time was removed, polymerization was carried out with strong stirring, and the polymer was taken out after cooling, and the yield was 10.8
The weight was 8 kg, which was 97.8% of the theoretical yield.

これをハンマーミルで粉砕し、2W以下の粒子とし、ロ
ータリーキルン中で窒素雰囲気下で280℃、5時間処
理したところ、350°C以上で熔融状態での光学異方
性が観察された。
This was ground in a hammer mill to obtain particles of 2W or less, and when treated in a rotary kiln at 280°C for 5 hours under a nitrogen atmosphere, optical anisotropy in the molten state was observed at 350°C or higher.

実施例1 参考例のポリエステルを用い、30鵬径のスクリュー型
押出機により、溶融紡糸を行った。
Example 1 Using the polyester of the reference example, melt spinning was performed using a screw type extruder with a diameter of 30 mm.

紡糸口金は孔径0.07mm、孔長0.14mm、30
2の孔数を持つものである。
The spinneret has a hole diameter of 0.07 mm, a hole length of 0.14 mm, and a diameter of 30 mm.
The number of holes is 2.

単糸デニール2.87(直径約17μm)の糸が得られ
、これを除湿した空気中で320’C,3時間処理した
A single yarn with a denier of 2.87 (about 17 μm in diameter) was obtained, which was treated in dehumidified air at 320°C for 3 hours.

得られた繊維の密度は1.40g/cc、強度は336
 kg/lB11” 、破断伸度は2.7%、弾性率は
12、 67on/m”である。
The density of the obtained fiber was 1.40 g/cc, and the strength was 336.
kg/lB11", elongation at break is 2.7%, and elastic modulus is 12.67 on/m".

この繊維を、シリコン系の油剤を付けた後、lC■当た
り1回の撚りとなるように撚り上げ、その上に赤い顔料
(魚の好む色)を含むエポキシ系の油剤を付けて軽度に
固めて釣糸とした。
After applying a silicone oil, the fibers are twisted so that there is one twist per 1C, and then an epoxy oil containing a red pigment (a color that fish prefers) is applied to lightly harden the fibers. I used it as a fishing line.

取扱も良好で、水中での沈み速度も早く、深さ約5mか
らの魚信も明確に確認できた。
It handled well, sank quickly in the water, and fish could be clearly seen from a depth of about 5 meters.

実施例2 参考例のポリエステルを用い、紡糸口金として孔径0.
12mm、孔長0,36胴、24の孔数を持つ物を用い
た以外は、実施例1と同様にして溶融紡糸を行った。デ
ニール29.8(直径約55μm)の糸が得られ、これ
を除湿した空気中で320°C13時間処理した。
Example 2 The polyester of the reference example was used as a spinneret with a pore size of 0.
Melt spinning was carried out in the same manner as in Example 1, except that a material having a diameter of 12 mm, a hole length of 0, 36 holes, and 24 holes was used. A yarn with a denier of 29.8 (about 55 μm in diameter) was obtained and treated in dehumidified air at 320° C. for 13 hours.

得られた繊維の密度は1.38g/cc、強度は205
kg/胴2、破断伸度は2.8%、弾性率は7 、 6
7on/m2である。
The density of the obtained fiber was 1.38 g/cc, and the strength was 205
kg/body 2, elongation at break 2.8%, modulus of elasticity 7, 6
7on/m2.

この繊維を実施例1と同様に処理し、後加工した。This fiber was treated and post-processed in the same manner as in Example 1.

実施例1の釣糸と同様に、取扱も良好で、水中での沈み
速度も早く、深さ約5mからの魚信も明確に確認できた
As with the fishing line of Example 1, it was easy to handle, had a fast sinking speed in water, and was clearly able to catch fish from a depth of about 5 m.

Claims (1)

【特許請求の範囲】[Claims] 引っ張り破断強度が100kg/mm^2以上、密度1
.38g/cc以上の芳香族ポリエステル繊維からなる
釣糸。
Tensile breaking strength is 100kg/mm^2 or more, density 1
.. Fishing line made of aromatic polyester fiber of 38 g/cc or more.
JP62152765A 1987-06-18 1987-06-18 Fishing line Expired - Fee Related JP2522947B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62152765A JP2522947B2 (en) 1987-06-18 1987-06-18 Fishing line

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62152765A JP2522947B2 (en) 1987-06-18 1987-06-18 Fishing line

Publications (2)

Publication Number Publication Date
JPS63317032A true JPS63317032A (en) 1988-12-26
JP2522947B2 JP2522947B2 (en) 1996-08-07

Family

ID=15547658

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62152765A Expired - Fee Related JP2522947B2 (en) 1987-06-18 1987-06-18 Fishing line

Country Status (1)

Country Link
JP (1) JP2522947B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5714230A (en) * 1993-11-18 1998-02-03 Mitsui Toatsu Chemicals, Inc. Degradable aliphatic polyester formed products
JP2007135500A (en) * 2005-11-21 2007-06-07 Toray Monofilament Co Ltd Fishing line and method for producing the same

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS602710A (en) * 1983-06-17 1985-01-09 Unitika Ltd Polyester monofilament having high knot strength
JPS60164421A (en) * 1984-02-07 1985-08-27 東洋紡績株式会社 New fishing line
JPS61617A (en) * 1984-06-12 1986-01-06 Unitika Ltd Polyester monofilament
JPS63264914A (en) * 1987-04-21 1988-11-01 Unitika Ltd High-strength fiber

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS602710A (en) * 1983-06-17 1985-01-09 Unitika Ltd Polyester monofilament having high knot strength
JPS60164421A (en) * 1984-02-07 1985-08-27 東洋紡績株式会社 New fishing line
JPS61617A (en) * 1984-06-12 1986-01-06 Unitika Ltd Polyester monofilament
JPS63264914A (en) * 1987-04-21 1988-11-01 Unitika Ltd High-strength fiber

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5714230A (en) * 1993-11-18 1998-02-03 Mitsui Toatsu Chemicals, Inc. Degradable aliphatic polyester formed products
US5763098A (en) * 1993-11-18 1998-06-09 Mitsui Chemicals, Inc. Degradable aliphatic polyester formed products
JP2007135500A (en) * 2005-11-21 2007-06-07 Toray Monofilament Co Ltd Fishing line and method for producing the same

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