JPH0316088B2 - - Google Patents
Info
- Publication number
- JPH0316088B2 JPH0316088B2 JP7752583A JP7752583A JPH0316088B2 JP H0316088 B2 JPH0316088 B2 JP H0316088B2 JP 7752583 A JP7752583 A JP 7752583A JP 7752583 A JP7752583 A JP 7752583A JP H0316088 B2 JPH0316088 B2 JP H0316088B2
- Authority
- JP
- Japan
- Prior art keywords
- nylon
- weight
- thread
- strength
- plasticizer
- 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
Links
- 239000004014 plasticizer Substances 0.000 claims description 20
- 239000003086 colorant Substances 0.000 claims description 19
- 229920002292 Nylon 6 Polymers 0.000 claims description 12
- -1 polyethylene Polymers 0.000 claims description 11
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 10
- 239000004698 Polyethylene Substances 0.000 claims description 9
- 229920000573 polyethylene Polymers 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 5
- 238000002074 melt spinning Methods 0.000 claims description 4
- 229920001778 nylon Polymers 0.000 description 15
- 239000004677 Nylon Substances 0.000 description 12
- 239000004952 Polyamide Substances 0.000 description 11
- 229920002647 polyamide Polymers 0.000 description 11
- 238000005299 abrasion Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 229920000577 Nylon 6/66 Polymers 0.000 description 6
- TZYHIGCKINZLPD-UHFFFAOYSA-N azepan-2-one;hexane-1,6-diamine;hexanedioic acid Chemical compound NCCCCCCN.O=C1CCCCCN1.OC(=O)CCCCC(O)=O TZYHIGCKINZLPD-UHFFFAOYSA-N 0.000 description 6
- 239000011435 rock Substances 0.000 description 6
- 241000270506 Tupinambis Species 0.000 description 4
- 229920001903 high density polyethylene Polymers 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007850 fluorescent dye Substances 0.000 description 3
- 239000004700 high-density polyethylene Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- IPRJXAGUEGOFGG-UHFFFAOYSA-N N-butylbenzenesulfonamide Chemical compound CCCCNS(=O)(=O)C1=CC=CC=C1 IPRJXAGUEGOFGG-UHFFFAOYSA-N 0.000 description 2
- 229920000305 Nylon 6,10 Polymers 0.000 description 2
- 229920000572 Nylon 6/12 Polymers 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 2
- 239000004808 2-ethylhexylester Substances 0.000 description 1
- UFFRSDWQMJYQNE-UHFFFAOYSA-N 6-azaniumylhexylazanium;hexanedioate Chemical compound [NH3+]CCCCCC[NH3+].[O-]C(=O)CCCCC([O-])=O UFFRSDWQMJYQNE-UHFFFAOYSA-N 0.000 description 1
- JNSAWGNVZMPYJI-UHFFFAOYSA-N CCNS(=O)=O Chemical compound CCNS(=O)=O JNSAWGNVZMPYJI-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 241000276420 Lophius piscatorius Species 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- ZMUCVNSKULGPQG-UHFFFAOYSA-N dodecanedioic acid;hexane-1,6-diamine Chemical compound NCCCCCCN.OC(=O)CCCCCCCCCCC(O)=O ZMUCVNSKULGPQG-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 229920006017 homo-polyamide Polymers 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- DKYVVNLWACXMDW-UHFFFAOYSA-N n-cyclohexyl-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1CCCCC1 DKYVVNLWACXMDW-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
Description
(技術分野)
本発明は改良されたナイロンテグスに関するも
のである。さらに詳しくは高強度で柔軟性に富
み、かつ耐摩耗性にすぐれた着色ナイロンテグス
に関するものである。
(背景技術)
魚釣り用の道糸、ハリス、リール巻糸、ふかせ
およびルアーなどのいわゆるテグスとしては、従
来ナイロンテグスやテトロンテグスが主に用いら
れているが、とくにナイロンテグスにおいてはテ
グスに適度の柔軟性を付与するために、素材たる
ナイロンに対し可塑剤を含有せしめて実用に供す
る場合が多い。しかるにかかる可塑剤を配合した
可塑化ナイロンからなるテグスはその柔軟性こそ
改良されるものの、反面テグスの引張強力や結節
強力に代表される強度が可塑剤により阻害される
という問題がある。
また一般にナイロンテグスは透明で釣り人にと
つて見分けにくく、たとえば、たな取りなどの際
の目測が困難なため、通常は蛍光染料などの着色
剤を含有せしめた形で用いられているが、この場
合には着色剤の分散性に問題があり、テグスの強
度および柔軟性が阻害されることになる。このよ
うな欠点を改良するためには、たとえば特開昭52
−61592号公報に示されるように、蛍光染料成分
とナイロンモノマーとを予め反応させ、次にその
変性モノマーを重合し、さらにこのポリアミドに
可塑剤を混合して紡糸することにより、着色さ
れ、しかも柔軟性などの特性がすぐれたナイロン
テグスを得る方法が提案されているが、この方法
は蛍光染料成分が特殊であり、ナイロンモノマー
との反応工程が繁雑で、生産効率が劣るという問
題がある。
一方、通常の着色およびまたは可塑化したナイ
ロンテグスはその耐摩耗性が劣るために、使用中
に岩石との接触によりいわゆる岩ずれを生起して
テグス表面が傷つけられ、それに起因して糸切れ
を起こしやすいという欠点があり、たとえ引張強
力や柔軟生を十分満足したとしても岩ずれによる
テグスの損傷は避け難い。
(発明の目的)
本発明はこのような事情に鑑みなされたもの
で、特に所望の程度に着色され、しかも高強度で
柔軟性に富み、かつ耐摩耗性にすぐれ、岩ずれを
起こさないナイロンテグスを提供することを目的
とするものである。
(発明の開示)
本発明者らは上記の目的を達成するために、可
塑剤および着色剤を含有するナイロンテグスを改
良し、その欠点を解消すべく鋭意検討した結果、
素材ナイロンとして特定のかなり高い相対粘土を
有するポリカプロラクタムまたはカプロラクタム
を主体とするコポリアミドを用い、これに可塑剤
および着色剤の特定量と共にさらにポリエチレン
を特定量配合した組成物を溶融紡糸することによ
り、所望の色調を有し、しかも可塑剤や着色剤の
配合による強度および柔軟性の低下が抑制されて
ナイロンテグス本来の強度および可塑化効果が良
好に保持され、かつ耐摩耗性が極めて改良された
着色・可塑化ナイロンテグスが得られることを見
出し、本発明を完成するにいたつた。
すなわち本発明は相対粘度3.50〜4.00のポリカ
プロラクタムまたはカプロラクタムを50重量%以
上含有するコポリアミドに対し、可塑剤3〜10重
量%、着色剤0.05〜0.5重量%およびポリエチレ
ン0.5〜5重量%を配合した組成物を溶融紡糸し
てなるテグスを提供するものである。
本発明で使用するポリマ素材はポリカプロラク
タム(以下ナイロン6と呼ぶ)およびカプロラク
タムを50重量%以上含有するコポリアミドであ
り、ここでいうコポリアミドとしてはナイロン
6/66、ナイロン6/6I、ナイロン6/6T、ナ
イロン6/610、ナイロン6/612、ナイロン6/
12、ナイロン6/66/6I、ナイロン6/66/610、
ナイロン6/66/12、およびナイロン6/11など
が挙げられるが、中でもカプロラクタム75〜95重
量%およびヘキサメチレンジアンモニウムアジペ
ート25〜5重量%からなるナイロン6/66が最も
好ましく使用される。なおこれらナイロン6又は
コポリアミドに他のホモポリアミド又はコポリア
ミドを少割合ブレンドして用いることもできる。
これらのナイロン6およびコポリアミドは98%濃
硫酸にポリマを1重量%溶解した溶液をオストワ
ルド粘度計を用いて25℃で測定した相対粘度
(ηγ)が3.50〜4.50、とくに3.60〜4.00の範囲にあ
ることが重要であり、ηγが3.50未満では、製糸性
が劣るばかりか十分の強度が得られず、また4.50
を越えると紡糸が困難になるため好ましくない。
本発明で用いる可塑剤としてはN−エチル−
o・p−トルエンスルホンアミド、N−nブチル
−ベンゼンスルホンアミド、p−トルエンスルホ
ンアミド、N−シクロヘキシル−p−トルエンス
ルホンアミドおよびN−nブチル−p−トルエン
スルホンアミドなどのスルホンアミド系可塑剤、
p−オキシ安息香酸−2−エチルヘキシルエステ
ルなどの安息香酸エステル系可塑剤および2−メ
チル−2.4−ペンタンジオールなどのアルコール
系可塑剤などが使用できるが、なかでもスルホン
アミド系可塑剤により好ましい効果が得られる。
これら可塑剤の添加量はポリアミドに対して1〜
10重量%、とくに3〜8重量%が適当であり、1
重量%未満では柔軟性が不十分であり、8重量%
を越えると強度の低下が大きくなるため好ましく
ない。
本発明で用いる着色剤としては通常ポリアミド
の着色に使用されている種々の染料、顔料をとく
に制限せず、フタロシアニン系、アゾ系、バツト
系、ジオキサジン系、キナクリドン系などの有機
着色剤、カドミウム系、ベンガラ系、銅系などの
無機着色剤および有機・無機の蛍光着色剤などか
ら所望のものを選択することができるが、なかで
もオレンジまたはイエロー系の蛍光着色剤の使用
が適当である。なお、これらの着色剤はポリアミ
ドの重合時に添加(原着)することもできる。着
色剤の添加量はポリアミドに対し0.05〜0.5重量
%、とくに0.1〜0.4重量%が好ましく、0.05重量
%未満では望ましい着色の程度が得られず、0.5
重量%を越えると強度の低下が大きくなるため好
ましくない。
本発明で用いるポリエチレンは、上記ポリアミ
ド、可塑剤および着色剤からなるテグスの耐摩耗
性を改良し、しかも強度を良好に保持するために
作用する。そのポリエチレンとしては通常市販さ
れている低、中および高密度ポリエチレンのいず
れもが使用可能であるが、なかでも高密度ポリエ
チレン、とくにメルトインデツクスの高い高密度
ポリエチレンを使用する際に最も望ましい効果が
得られる。ポリエチレンの添加量はポリアミドに
対して0.1〜5重量%、とくに0.3〜3重量%が適
当であり、0.5重量%未満では耐摩耗性の改良効
果が小さく、また5重量%を越えるとポリアミド
自体の強度等のすぐれた特性が阻害されるため好
ましくない。
本発明のテグスを製造するに際しては通常の溶
融紡糸、延伸および熱固定条件をそのまま適用す
ることができる。たとえばポリアミドの重合時に
可塑剤と着色剤を添加して、この原着・可塑化ポ
リアミドにポリエチレンを添加する方法、原着ポ
リアミドに可塑剤とポリエチレンを添加する方法
およびポリアミド、可塑剤、着色剤およびポリエ
チレンの4者を同時に混合する方法などにより組
成物を得た後、これを押出機で溶融混合し、押出
紡糸する。次に紡出糸を必要に応じて冷却した
後、適宜倍率、たとえば3〜8倍に延伸し、さら
に必要に応じ熱固定することにより所望のモノフ
イラメント(テグス)が得られる。テグスの繊度
は40〜4400デニールが適当であり、テグスの用途
に応じてその太さが選択できる。得られたテグス
は駒巻き或いはかせ状にし製品とされる。
かくしてなる本発明のテグスは高強度で柔軟性
に富み、かつ耐摩耗性にすぐれ糸切れを起こしに
くい着色テグスであり、その繊度に応じて各種の
魚釣り用糸として広く活用が期待できる。
以下に実施例を挙げて本発明をさらに説明す
る。
実施例
相対粘度3.70のナイロン6/66(90/10重量比)
ペレツトに対し、可塑剤としてA.富士アミドケ
ミカル社製“Topcizer No.3”(H−エチル−op
−トルエンスルホンアミド)またはB.バスフ社
製“Plastomol BMB”(N−nブチルベンゼン
スルホンアミド)、着色剤として山陽化工社製
“G−8”(イエロー系蛍光顔料)および耐摩耗性
改良剤として三井石油化学社製“HI−
ZEX2100J”(高密度ポリエチレン、メルトイン
デツクス=6.5)をそれぞれ第1表の割合でドラ
イブレンドし、これを40mmΦの溶融押出機に供給
して溶融し、吐出量120g/分の条件で12ホール
の口金より紡出させた。次いで紡出糸を10℃の水
中で固化せしめた後、150℃で5.4倍に熱延伸を行
ない、それぞれ660デニールのモノフイラメント
(テグス)を得た。
得られた各テグスについて、各種の特性を評価
した結果を第1表に併せて示す。
なお、テグスの特性評価は次の方法により行な
つた。
強度…JISLI013の方法に準じて測定した。
柔軟性…5cmの長さに切断したテグスを、間隔が
10mmの二支点間に中央部が載るように置き、中
央部に荷重を与えてわん曲させ、テグスが二支
点間から抜け落ちる際の最大荷重値(g)を測
定した。
耐摩耗性…直径50mmの回転体表面に#320のサン
ドペーパーを巻きつけてこれを毎分180回転で
回転させる。一方テグスに33gの荷重をかけて
垂直にたらしこれを前記回転体に対し90゜の角
度で接触させ、テグスが切断するまでの回転体
の回転数(回)を測定した。
色調…肉眼観察。
(Technical Field) The present invention relates to an improved nylon thread. More specifically, it relates to colored nylon strings that are high in strength, highly flexible, and have excellent abrasion resistance. (Background technology) Conventionally, nylon threads and Tetron threads have been mainly used as fishing threads such as fishing line, Harris, reel winding line, floats, and lures. In order to impart flexibility to the material, nylon is often used in practical applications by incorporating a plasticizer into it. However, although the flexibility of strings made of plasticized nylon blended with such plasticizers is improved, on the other hand, there is a problem in that the strength of the strings, represented by the tensile strength and knot strength, is inhibited by the plasticizer. In addition, nylon fishing rods are generally transparent and difficult to distinguish for anglers, making it difficult to visually assess them when fishing, for example, so they are usually used in a form containing a coloring agent such as fluorescent dye. In this case, there is a problem with the dispersibility of the colorant, which impairs the strength and flexibility of the string. In order to improve such shortcomings, for example,
As shown in Japanese Patent No. 61592, the fluorescent dye component and the nylon monomer are reacted in advance, the modified monomer is polymerized, and the polyamide is mixed with a plasticizer and spun to obtain colored, and A method for obtaining nylon fibers with excellent properties such as flexibility has been proposed, but this method uses a special fluorescent dye component, requires a complicated reaction process with the nylon monomer, and has the problem of poor production efficiency. On the other hand, ordinary colored and/or plasticized nylon threads have poor abrasion resistance, so when they come into contact with rocks during use, they cause so-called rock shear, which damages the surface of the threads and causes thread breakage. It has the disadvantage of being easily damaged by rock slippage, and even if the tensile strength and flexibility are sufficiently satisfied, it is difficult to avoid damage to the threads caused by rock slips. (Purpose of the Invention) The present invention was made in view of the above circumstances, and specifically provides a nylon thread that is colored to a desired degree, has high strength and flexibility, has excellent abrasion resistance, and does not cause rock slippage. The purpose is to provide the following. (Disclosure of the Invention) In order to achieve the above object, the present inventors improved nylon fibers containing plasticizers and colorants, and as a result of intensive studies to eliminate their drawbacks,
By melt-spinning a composition in which polycaprolactam or a copolyamide mainly composed of caprolactam, which has a specific fairly high relative clay content, is used as the material nylon, and a specific amount of polyethylene is further blended with the specific amount of a plasticizer and colorant. , has the desired color tone, suppresses the decrease in strength and flexibility due to the combination of plasticizers and colorants, maintains the original strength and plasticizing effect of nylon thread well, and has extremely improved abrasion resistance. They discovered that colored and plasticized nylon fibers can be obtained and completed the present invention. That is, the present invention blends 3 to 10 weight % of a plasticizer, 0.05 to 0.5 weight % of a colorant, and 0.5 to 5 weight % of polyethylene to polycaprolactam or a copolyamide containing 50 weight % or more of caprolactam with a relative viscosity of 3.50 to 4.00. The purpose of the present invention is to provide a thread formed by melt-spinning the composition. The polymer materials used in the present invention are polycaprolactam (hereinafter referred to as nylon 6) and copolyamides containing 50% by weight or more of caprolactam, and the copolyamides mentioned here include nylon 6/66, nylon 6/6I, and nylon 6. /6T, nylon 6/610, nylon 6/612, nylon 6/
12, nylon 6/66/6I, nylon 6/66/610,
Examples include nylon 6/66/12 and nylon 6/11, among which nylon 6/66, which is composed of 75 to 95% by weight of caprolactam and 25 to 5% by weight of hexamethylene diammonium adipate, is most preferably used. Note that a small proportion of other homopolyamides or copolyamides may be blended with these nylon 6 or copolyamides.
These nylon 6 and copolyamides have a relative viscosity (ηγ) in the range of 3.50 to 4.50, particularly 3.60 to 4.00, measured at 25°C using an Ostwald viscometer using a solution of 1% by weight of the polymer dissolved in 98% concentrated sulfuric acid. It is important that
Exceeding this is not preferable because spinning becomes difficult. The plasticizer used in the present invention is N-ethyl-
Sulfonamide plasticizers such as o.p-toluenesulfonamide, N-nbutyl-benzenesulfonamide, p-toluenesulfonamide, N-cyclohexyl-p-toluenesulfonamide and N-nbutyl-p-toluenesulfonamide. ,
Benzoate ester plasticizers such as p-oxybenzoic acid-2-ethylhexyl ester and alcohol plasticizers such as 2-methyl-2,4-pentanediol can be used, but sulfonamide plasticizers have particularly favorable effects. can get.
The amount of these plasticizers added is 1 to 1 to
10% by weight, especially 3 to 8% by weight, is suitable;
If it is less than 8% by weight, the flexibility is insufficient;
Exceeding this is not preferable because the strength decreases significantly. The coloring agent used in the present invention is not particularly limited to various dyes and pigments that are normally used for coloring polyamides, and includes organic colorants such as phthalocyanine, azo, butt, dioxazine, and quinacridone, and cadmium. Desired colorants can be selected from inorganic colorants such as , red iron type, copper type, and organic/inorganic fluorescent colorants, among which orange or yellow type fluorescent colorants are suitable. Incidentally, these colorants can also be added (dosing) during polymerization of polyamide. The amount of the coloring agent added is preferably 0.05 to 0.5% by weight, particularly 0.1 to 0.4% by weight, based on the polyamide. If it is less than 0.05% by weight, the desired degree of coloring cannot be obtained;
Exceeding this percentage by weight is not preferable because the strength decreases significantly. The polyethylene used in the present invention functions to improve the abrasion resistance of the thread made of the above-mentioned polyamide, plasticizer, and colorant, and to maintain good strength. Commercially available low, medium, and high density polyethylenes can all be used as the polyethylene, but the most desirable effect is achieved when using high density polyethylene, especially high density polyethylene with a high melt index. can get. The appropriate amount of polyethylene to be added is 0.1 to 5% by weight, especially 0.3 to 3% by weight, based on the polyamide.If it is less than 0.5% by weight, the effect of improving wear resistance will be small, and if it exceeds 5% by weight, the polyamide itself will deteriorate. This is not preferable because it impairs excellent properties such as strength. When producing the threads of the present invention, ordinary melt spinning, stretching and heat setting conditions can be applied as they are. For example, a method in which a plasticizer and a coloring agent are added during the polymerization of polyamide and then polyethylene is added to the spun-dyed and plasticized polyamide, a method in which a plasticizer and polyethylene are added to a spun-dyed polyamide, and a method in which a plasticizer and a coloring agent are added to the spun-dyed polyamide; After a composition is obtained by a method of simultaneously mixing four polyethylenes, this is melt-mixed in an extruder and extrusion-spun. Next, the spun yarn is cooled as necessary, then stretched to an appropriate magnification, for example, 3 to 8 times, and further heat-set as necessary to obtain a desired monofilament (tegus). The appropriate fineness of the thread is 40 to 4,400 deniers, and the thickness can be selected depending on the purpose of the thread. The obtained tegus is made into pieces or skeins and made into products. The thus-formed thread of the present invention is a colored thread that is highly strong, highly flexible, has excellent abrasion resistance, and is resistant to thread breakage, and can be expected to be widely used as a variety of fishing lines depending on its fineness. The present invention will be further explained below with reference to Examples. Example Nylon 6/66 (90/10 weight ratio) with a relative viscosity of 3.70
A. “Topcizer No. 3” manufactured by Fuji Amido Chemical Co., Ltd. (H-ethyl-op) was used as a plasticizer for the pellets.
- toluenesulfonamide) or "Plastomol BMB" (N-n butylbenzenesulfonamide) manufactured by B. Basf, "G-8" manufactured by Sanyo Kako Co., Ltd. (yellow fluorescent pigment) as a coloring agent and as a wear resistance improver. Mitsui Petrochemical Co., Ltd. “HI-”
ZEX2100J" (high-density polyethylene, melt index = 6.5) was dry blended at the ratio shown in Table 1, and this was fed into a 40 mmΦ melt extruder and melted. The yarn was spun from a spinneret.Then, the spun yarn was solidified in water at 10°C, and then hot-stretched to 5.4 times at 150°C to obtain monofilaments of 660 denier. Table 1 shows the results of evaluating the various properties of TEGUS. The characteristics of TEGUS were evaluated using the following methods. Strength: Measured according to the JISLI013 method. Flexibility: 5 cm Cut the strings to length, and then
The center part was placed between two 10 mm fulcrums, a load was applied to the center part to bend it, and the maximum load value (g) when the thread fell out from between the two fulcrums was measured. Abrasion resistance: Wrap #320 sandpaper around the surface of a rotating body with a diameter of 50 mm and rotate it at 180 revolutions per minute. On the other hand, a load of 33 g was applied vertically to the thread, and it was brought into contact with the rotating body at an angle of 90°, and the number of rotations (times) of the rotating body until the thread was cut was measured. Color tone: Observation with the naked eye.
【表】【table】
【表】
第1表から明らかなように、本発明のテグスは
高強度で柔軟性がすぐれ、しかも耐摩耗性が著し
く改良されており、実際に海釣り用道糸として使
用した際にも、蛍光色で見分け易く、すべりがよ
く、さおにはりつかず、海底の岩などに接触して
も傷がつきにくいすぐれた特性を発揮した。[Table] As is clear from Table 1, the threads of the present invention have high strength and excellent flexibility, and have significantly improved abrasion resistance, and when actually used as sea fishing line, It is easy to distinguish due to its fluorescent color, has good sliding properties, does not stick to rods, and exhibits excellent properties such as being resistant to scratches even when it comes into contact with rocks on the ocean floor.
Claims (1)
たはカプロラクタムを50重量%以上含有するコポ
リアミドに対し、可塑剤1〜10重量%、着色剤
0.05〜0.5重量%およびポリエチレン0.1〜5重量
%を配合した組成物を溶融紡糸してなるテグス。1 Polycaprolactam with a relative viscosity of 3.50 to 4.50 or a copolyamide containing 50% by weight or more of caprolactam, 1 to 10% by weight of a plasticizer, and a colorant.
Tegusu is made by melt-spinning a composition containing 0.05 to 0.5% by weight and 0.1 to 5% by weight of polyethylene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7752583A JPS59203439A (en) | 1983-05-04 | 1983-05-04 | Gut |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7752583A JPS59203439A (en) | 1983-05-04 | 1983-05-04 | Gut |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59203439A JPS59203439A (en) | 1984-11-17 |
JPH0316088B2 true JPH0316088B2 (en) | 1991-03-04 |
Family
ID=13636386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7752583A Granted JPS59203439A (en) | 1983-05-04 | 1983-05-04 | Gut |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59203439A (en) |
-
1983
- 1983-05-04 JP JP7752583A patent/JPS59203439A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59203439A (en) | 1984-11-17 |
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