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JP3570171B2 - Method for producing core-sheath composite fiber and method for producing false twisted yarn comprising the same - Google Patents
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JP3570171B2 - Method for producing core-sheath composite fiber and method for producing false twisted yarn comprising the same - Google Patents

Method for producing core-sheath composite fiber and method for producing false twisted yarn comprising the same Download PDF

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JP3570171B2
JP3570171B2 JP22797897A JP22797897A JP3570171B2 JP 3570171 B2 JP3570171 B2 JP 3570171B2 JP 22797897 A JP22797897 A JP 22797897A JP 22797897 A JP22797897 A JP 22797897A JP 3570171 B2 JP3570171 B2 JP 3570171B2
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spinning
fiber
core
elongation
sheath
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JPH1161572A (en
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隆志 越智
基忠 福原
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Toray Industries Inc
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Toray Industries Inc
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  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)

Description

【0001】
【発明の属する技術分野】
本発明は、吐出量増加によって生産性を向上させると共に、発色性、染め斑および耐摩耗特性などの品質が改善された芯鞘複合繊維の製造法に関するものである。
【0002】
【従来の技術】
ポリエチレンテレフタレート(以下PETと略す)繊維は、機械的特性をはじめとして様々の優れた特性を有しているため、衣料用途はもとより産業資材用途にも広く利用されている。
【0003】
近年、PET繊維の製造においては、紡糸における引取速度を5000m/分以上と高速にして、延伸工程を経ることなく、1工程で実用的な繊維を得る高速紡糸法が工業的に採用されている。紡糸工程における生産性は単位時間当りの吐出量に大きく依存するため、高速にすればするほどこのような1工程法の生産性は向上する。
【0004】
しかしながら、高速紡糸方法において、PET繊維は、6000〜7000m/分付近の紡糸速度では実用上好ましい機械特性を示すが、さらに高速化していくと強伸度が低下し、実用上に問題を生ずる。そのため生産性向上の効果を十分に発揮するには限界がある。
【0005】
そこで、同一紡糸速度でも、分子配向を抑制し残留伸度のより大きな繊維を得ることができれば、さらに紡糸速度を高くする、すなわち吐出量を増大させ、生産効率を高めることが可能となる。
【0006】
この点に関して、特開平8−246247号公報にはPETに対してポリスチレン、ポリメチルメタクリレート、ポリメチルペンテンなどを芯成分として複合することにより、得られる繊維の残留伸度が増大し、紡糸の生産性が大幅に向上することが示されている。しかしながら、芯成分として挙げられたこれらのポリマは、PET用の通常の染料には染まらないため染色品の発色性に問題を生じたり、染め斑が発生することが判明した。また、染色後に芯鞘界面での剥離が発生するため、摩擦に対して鞘割れやフィブリル化が発生しやすく耐摩耗特性に問題があることも判明した。
【0007】
【発明が解決しようとする課題】
本発明は、吐出量増加による生産性を向上させると共に、発色性、染め斑および耐摩耗特性の問題点を解決するため、検討を重ねた結果得られたものである。
【0008】
換言すれば、PETを高速紡糸する際に生じる繊維の発色性、染め斑および耐摩耗特性の問題点を解決せんとするものである。
【0009】
【課題を解決するための手段】
本発明の目的は、鞘成分が実質的にポリエチレンテレフタレートからなるポリエステル、芯成分が5−ナトリウムスルホイソフタル酸が2〜15モル%共重合されたポリエステルからなり、芯成分複合比が1〜15重量%である芯鞘複合繊維を紡糸速度4000〜12000m/分で紡糸することにより達成される。
【0010】
【発明の実施の形態】
以下本発明について詳細に説明する。
【0011】
鞘成分におけるPETは、ジオール成分および酸成分の一部が各々15モル%以下の範囲で他の共重合可能な成分で置換されたものであってもよい。また、これらは艶消剤、難燃剤、帯電防止剤、顔料などの添加物を含有していてもよい。
【0012】
芯成分ポリマは、5−ナトリウムスルホイソフタル酸が2〜15モル%共重合されたポリエステルであれば紡糸速度の高速化と染色性、耐摩耗特性が両立される。
【0013】
5−ナトリウムスルホイソフタル酸の共重合率は高い方が生産性向上効果が高く好ましいが、過度に共重合率を高くすると重合過程で急激な増粘が発生し、ポリマの重合度を上げることができないという問題が生じてしまう。また、ポリマの熱安定性も低下するため紡糸性が悪化してしまう。5−ナトリウムスルホイソフタル酸の共重合率は2〜15モル%であれば紡糸性が良好である。好ましくは5〜12モル%である。
【0014】
また、芯成分ポリマには本発明を達成することができる範囲であれば、5−ナトリウムスルホイソフタル酸の他にイソフタル酸等が共重合されていても差し支えない。
【0015】
なお、本発明でいう5−ナトリウムスルホイソフタル酸の共重合率とは、ポリマ中の全酸成分に対する5−ナトリウムスルホイソフタル酸のモル比をいうものとする。
【0016】
また、芯成分ポリマは、5−ナトリウムスルホイソフタル酸共重合ポリエステル単独でもよいし、本発明の効果を発現する範囲であればナイロン等他のポリマと混合したものでもよい。
【0017】
芯鞘形状には特に制限はなく、同心円芯鞘でも偏芯芯鞘でもよいし、芯が複数あるようなものでも海島構造をしているものでもよい。つまり、芯成分ポリマが繊維軸方向に一定の量で連続的に存在し、さらに繊維表面に露出していないことが好ましい。したがって、発色性や耐摩耗特性等の点から芯ポリマはできるだけ中央に集めた同心円芯鞘が好ましい。
【0018】
5−ナトリウムスルホイソフタル酸共重合ポリエステルが鞘側となると、高速紡糸過程において鞘側が急冷されるため共重合ポリマの悪影響が顕在化しやすく、紡糸不調となったり、得られた繊維にミクロボイド等の欠陥が多く発生し脆くなるため残留伸度向上効果が発現せず、さらに強度も低くなる。この急冷による悪影響は低速紡糸の場合はさほど問題にならないが、紡糸速度が高速になるほどその影響が急激に大きくなる。高速紡糸ではホモPET単独糸でさえ急冷により繊維物性が低下することが“HIGH−SPEED FIBER SPINNING”447頁(WILEY−INTERSCIENCE)等に記載されている。そのため本発明のように、共重合ポリエステルポリマを使用し高速紡糸を行う場合は特に注意が必要である。特に、紡糸速度が6000m/分以上では共重合ポリエステルを鞘にすると実用に耐えうる繊維を得ることはほとんど困難である。実際、5−ナトリウムスルホイソフタル酸共重合ポリエステルを鞘側にして高速紡糸を行うことが特開昭64−14333号公報、特開平5−9855号公報に開示されているが、いずれも複合紡糸により得られた繊維の残留伸度が増加する効果は認められていないだけでなく、強度が低くフィラメントとして衣料用や産業資材用途に用いることは困難である。
【0019】
紡糸により得られた繊維の残留伸度が70%以上のいわゆる高配向未延伸糸(POY)の性質を有するものでは、さらに延伸や延伸仮撚を施すことが好ましい。その時の加工性、工程安定性を考慮すると得られる繊維はある程度配向していた方がよいと考えられる。そのため紡糸速度は4000m/分以上であることが好ましい。
【0020】
通常延伸仮撚加工用のPETの高配向未延伸糸は紡糸速度3000m/分程度で生産されている。紡糸速度4000m/分で得られる繊維でも延伸仮撚加工は不可能ではないが、得られる加工糸の残留伸度が過度に低下するため、紡糸速度3000m/分で得られた繊維の場合に比べ延伸倍率を大幅に下げる必要がある。そのため、紡糸/延伸仮撚加工の総合的な生産性は必ずしも上昇するわけではなく好ましくない。また、生産性に見合うよう延伸倍率を高くして加工を施すと、加撚/解撚部の張力が過度に上昇するため毛羽立ちや糸切れを生じやすく、延伸仮撚加工の操業性が低下する。
【0021】
これに対し、本発明では5−ナトリウムスルホイソフタル酸共重合ポリエステルを特定量複合繊維の芯として配置することにより、紡糸速度を高くしても得られる高配向未延伸糸の配向度は抑制され、紡糸/延伸仮撚加工の生産性が向上するものである。
【0022】
一方、紡糸により得られた繊維の残留伸度が70%未満のものは、特別な延伸工程を必要とせずそのままでも衣料用途に使用できる。この時は生産性の点から紡糸速度は8000m/分以上が好ましい。本発明によれば、従来、強伸度が低く実用に耐えなかった紡糸速度8000m/分はもとより紡糸速度を10000m/分以上としても強伸度の低下が小さく、衣料用として実用に耐えうる繊維を得ることができる。そして、この高速紡糸によって得られた繊維に仮撚加工を施すこともできる。
【0023】
上記した配向度上昇の抑制効果は、その目的に応じて芯成分の複合比として1重量%以上、好ましくは3重量%以上である。芯成分複合比が1重量%未満では十分な配向抑制効果を期待することはできない。一方、芯成分複合比を高くするにつれ配向抑制効果は顕著となっていくが、最終製品の強度や仮撚り加工時の繊維断面変形、熱セット性等を考慮すると15重量%以下、好ましくは10重量%以下である。
【0024】
本発明では共重合ポリエステルを比較的少量芯に配置せしめているため、高温熱処理を行っても融着等のトラブルを生じることがない。また鞘成分PETとの相溶性が高いため芯/鞘界面での剥離を生じることもなく、耐摩耗特性も良好である。さらに、芯成分の方が鞘成分よりも染色性が高くなり、発色性が向上するだけでなく摩擦による変色特性(フロスティング特性)も向上する。
【0025】
5−ナトリウムスルホイソフタル酸はPETの改質剤としては非常によく知られているポリマである。その共重合ポリマは、染色性、アルカリ溶出性等の向上を目的として広く用いられている。しかしながら、5−ナトリウムスルホイソフタル酸共重合ポリエステルは複合繊維の場合は繊維に機能性を持たせるため鞘部に用いられることがほとんどであり、本発明のごとく、5−ナトリウムスルホイソフタル酸共重合ポリエステルを特定量複合させるだけでPET繊維の配向が抑制されるという効果は全く知られていなかった。
【0026】
このように5−ナトリウムスルホイソフタル酸共重合ポリエステルが高速紡糸によってPETの配向を抑制し、得られる繊維の残留伸度が増加する理由は明らかではないが、芯ポリマの存在が紡糸中の繊維の細化挙動に影響を及ぼし、鞘PETの配向構造が形成される際にその内部応力を低減させることによりPETの配向が抑制されるものと思われる。
【0027】
本発明によれば4000〜6000m/分の高速紡糸においても、得られる繊維は1.2〜2.0倍の延伸倍率での延伸(仮撚)加工が可能であり、従来より生産性の優れた製法である。また、PET単独での高速紡糸では紡糸速度8000m/分以上で得られた繊維は強伸度特性に劣るのに対し、本発明の方法では紡糸速度8000m/分以上でも実用的な強伸度特性を有する繊維を得ることができ、超高速紡糸においても従来より生産性の優れた製法である。
【0028】
本発明で得られたポリエステル繊維は、生糸のままで、あるいは撚糸、仮撚加工糸として、裏地、スポーツウエア、スラックス、ブルゾン、ブラウスなどの衣料用途や、リボン、テープ、ベルトなどの資材用途に好適に用いることができる。
【0029】
【実施例】
以下、本発明を実施例を用いて詳細に説明する。
【0030】
なお、実施例中の測定方法は以下の方法を用いた。
【0031】
A.極限粘度[η]
オルソクロロフェノール中25℃で測定した。
【0032】
B.応力−伸長曲線、強度および伸度
JIS L1013に従って、荷重−伸長曲線を求めた。
【0033】
次に荷重値を初期の繊度で割り、それを応力(強度)とし、伸びを初期試料長で割り強度、伸度からなる応力−伸長曲線を求めた。
【0034】
C.染色
繊維を筒編み後テラシルネイビーブルーSGLで染色し、発色性と染め斑の官能評価を行った。
【0035】
D.耐摩耗特性
繊維を筒編み、染色後、摩擦した後の編地の変色を官能評価した。
【0036】
実施例1
極限粘度0.63のホモPETと5−ナトリウムスルホイソフタル酸を12モル%共重合した極限粘度0.63の共重合ポリエステルを別々に溶融し、絶対濾過径5μのステンレス製不織布フィルタにより濾過した後、共重合ポリエステルを芯、ホモPETを鞘の同心円上の芯鞘複合にして孔径0.25mm、孔数36の口金から吐出した。この時の芯成分の複合比率は8重量%であった。紡糸温度は295℃、吐出量は単糸繊度4dtexになるように調整した。吐出した糸条は、吐出後常法により冷却、給油後交絡を付与し引取ローラーを介して巻取機で巻取った。糸条が最初に触れる引取ローラーの周速度を紡糸速度として表1に示す(実験No.1〜5)。この時、紡糸速度6000m/分および10000m/分で得られた繊維の応力−伸長曲線を図1の曲線Aおよび図2の曲線Aにそれぞれ示した。また強度および伸度を表1に示す。図−1および図−2には比較例−1の実験No.10および12の共重合していないPET単独糸の結果をそれぞれ曲線Bとして記載した。
【0037】
紡糸速度6000m/分糸(図1A)でもPET単独の場合(比較例1、図1B)とは異なり、本発明の複合繊維は定応力伸長領域を有し未延伸糸である。さらに、紡糸速度10000m/分糸(図2A)であっても、PET単独(比較例1、図2B)の場合とは異なり良好な強伸度特性を有していることがわかる。 また、表1から分かるように5−ナトリウムスルホイソフタル酸共重合ポリエステルをホモPETに複合させた場合、PET単独糸(実験No.9〜13)に比べ、全紡糸速度領域にわたって伸度向上の効果が得られた。
【0038】
紡糸速度4000および6000m/分で得られた繊維をヒーター温度220℃、延伸倍率をそれぞれ1.95、1.68倍で延伸仮撚加工を行った。延伸仮撚加工した繊維および紡糸速度8000〜12000m/分で得られた繊維そのものの発色性、染め斑および耐摩耗特性を表2に示す。延伸仮撚加工した繊維および紡糸速度8000m/分以上の超高速紡糸繊維とも発色性、染め斑および耐摩耗特性とも良好であった。
【0039】
実施例2
共重合ポリエステルを5−ナトリウムスルホイソフタル酸6モル%共重合(極限粘度0.65)とした以外は実施例1(実験No.2)と同様の条件で溶融紡糸を行った(実験No.6)。強度および伸度を表1に示す。この時も伸度向上効果がみられた。また、ヒーター温度220℃、延伸倍率1.32倍で、この繊維の延伸仮撚加工を行った。延伸仮撚加工した繊維の発色性、染め斑および耐摩耗特性とも良好であった(表2)。
【0040】
実施例3
共重合ポリエステルを5−ナトリウムスルホイソフタル酸2モル%共重合(極限粘度0.65)とした以外は実施例1(実験No2)と同様の条件で溶融紡糸を行った(実験No.7)。強度および伸度を表1に示す。この時も伸度向上効果は少なくなるが実施例−1の同一紡糸速度のものと比較して強度が改善されていることがわかる。また、ヒーター温度220℃、延伸倍率1.22倍でこの繊維の延伸仮撚加工を行った。延伸仮撚加工した繊維の発色性、染め斑および耐摩耗特性とも良好であった(表2)。
【0041】
実施例4
5−ナトリウムスルホイソフタル酸の共重合率を10モル%、さらにイソフタル酸を20モル共重合(極限粘度0.60)とした以外は実施例1(実験No.2)と同様の条件で紡糸を行った(実験No.8)。強度および伸度を表1に示す。この時も伸度向上効果がみられた。また、ヒーター温度220℃、延伸倍率1.60倍でこの繊維の延伸仮撚加工を行った。延伸仮撚加工した繊維の発色性、染め斑および耐摩耗特性とも良好であった(表2)。
【0042】
比較例1
ポリマを実施例1で用いたホモPETのみとし、それの単独糸を複合紡糸によらず実施例1と同様の条件で溶融紡糸を行った(実験No.9〜13)。強度および伸度を表1に示した。
【0043】
また、紡糸速度6000m/分および10000m/分で得られた繊維の応力−伸長曲線を図1の曲線Bおよび図2の曲線Bにそれぞれ示した。いづれも典型的なPET繊維の特性を示しており、紡糸速度6000m/分では既に巻取りまでで延伸が起こり定応力伸長領域を有さず未延伸糸とはなっていないことが分かる。
【0044】
そして、紡糸速度10000m/分糸では5−ナトリウムスルホイソフタル酸12モル%共重合ポリエステル複合の場合とは異なり、実用に耐えない強伸度特性となっている。また、ヒーター温度220℃、延伸倍率1.32倍で紡糸速度4000m/分で得られた繊維の延伸仮撚加工を行ったが、加工時に毛羽が多発した。延伸仮撚加工した繊維の発色性、染め斑および耐摩耗特性を表2に示した。
【0045】
実施例5
共重合ポリエステルの複合比率を5および14重量%とした以外は実施例1(No.2)と同様の条件で溶融紡糸を行った(実験No.14、15)。強度および伸度を表1に示す。複合比が大きくなるほど、伸度向上効果が大きいことが分かる。また、ヒーター温度220℃で、5重量%複合の繊維は延伸倍率1.32倍、14重量%複合の繊維は延伸倍率1.94倍で延伸仮撚加工を行った。
【0046】
延伸仮撚加工した繊維の発色性、染め斑および耐摩耗特性とも良好であった(表2)。
【0047】
比較例2
5−ナトリウムスルホイソフタル酸の共重合率を1(極限粘度0.65)および17モル%(極限粘度0.57)とした以外は実施例1(実験No.2)と同様の条件で紡糸を行った(実験No.16、17)。強度および伸度を表1に示した。共重合率1モル%では伸度向上効果はほとんど見られなかった。共重合率17モル%では伸度向上効果は大きかったが、紡糸調子が不調となり断糸が多発した、得られた繊維の強度も低いものであった。
【0048】
比較例3
共重合ポリエステルの複合比を18重量%とした以外は実施例2(実験No.6)と同様な条件で紡糸を行った(実験No.18)。強度および伸度を表1に示した。伸度向上効果は大きかったが、紡糸調子がやや不調であった。ヒーター温度220℃で、1.95倍で、この繊維の延伸仮撚加工を行った。しかし、加工時に毛羽が多発し、また、発色性、染め斑、対摩耗特性も劣ったものであった(表2)さらに延伸仮撚加工糸の強度が過度に低下する、断面変形が大きすぎる等の欠点もあった。
【0049】
比較例4
実施例3の芯ポリマと鞘ポリマを入れ替え、鞘ポリマ(5−ナトリウムスルホイソフタル酸2モル%共重合)複合比を10重量%とした以外は実施例3と同様の条件で溶融紡糸を行った(実験No.19)。この時は伸度がほとんど向上しなかったばかりか強度が大幅に低下した(表1)。さらに紡糸不調となり断糸が多発した。
【0050】
比較例5
実施例1の芯ポリマ(5−ナトリウムスルホイソフタル酸12モル%共重合)を複合ではなくブレンドとした以外は、実施例1と同様の条件で紡糸速度6000m/分で溶融紡糸を行った(実験No.20)。この時も若干の伸度向上効果は見られたが、紡糸不調となり断糸が多発した。
【0051】
【表1】

Figure 0003570171
【表2】
Figure 0003570171
【0052】
【発明の効果】
本発明の芯鞘複合繊維の製造法を採用することにより、単位時間当たりの吐出量を大幅に増加させることができ、しかも発色性、耐摩耗特性等の従来技術の欠点を克服することができる。換言すれば、ポリエチレンテレフタレートを高速紡糸する際に生じる繊維の発色性、染め斑および耐摩耗特性の問題点を解決できるものである。
【図面の簡単な説明】
【図1】本発明の実施例および比較例において、紡糸速度6000m/分で紡糸して得られた繊維の応力−伸長曲線を示す図である。
【図2】本発明の実施例および比較例において、紡糸速度10000m/分で紡糸して得られた繊維の応力−伸長曲線を示す図である。
【符号の説明】
A 5−ナトリウムスルホイソフタル酸共重合ポリエステルを芯、ホモPETを鞘とした芯鞘複合繊維
B PET単独繊維[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to a method for producing a core-in-sheath conjugate fiber in which productivity is improved by increasing the discharge amount, and in which the quality such as coloring property, spots and abrasion resistance is improved.
[0002]
[Prior art]
Polyethylene terephthalate (hereinafter abbreviated as PET) fibers have various excellent properties including mechanical properties, and are therefore widely used not only for clothing but also for industrial materials.
[0003]
In recent years, in the production of PET fibers, a high-speed spinning method in which a take-up speed in spinning is as high as 5,000 m / min or more and a practical fiber is obtained in one step without going through a drawing step has been industrially adopted. . Since the productivity in the spinning process greatly depends on the discharge amount per unit time, the higher the speed, the higher the productivity of such a one-step method.
[0004]
However, in the high-speed spinning method, PET fibers exhibit practically preferable mechanical properties at a spinning speed of about 6,000 to 7000 m / min, but when the speed is further increased, the strong elongation is reduced, which causes a problem in practical use. Therefore, there is a limit to sufficiently exhibit the effect of improving productivity.
[0005]
Therefore, if it is possible to obtain a fiber having a larger residual elongation while suppressing the molecular orientation even at the same spinning speed, it is possible to further increase the spinning speed, that is, to increase the discharge rate, thereby increasing the production efficiency.
[0006]
In this regard, Japanese Patent Application Laid-Open No. 8-246247 discloses that by combining PET with polystyrene, polymethyl methacrylate, polymethyl pentene, or the like as a core component, the residual elongation of the obtained fiber is increased, and the production of spun yarn is increased. It has been shown that the performance is greatly improved. However, it has been found that these polymers listed as the core component do not dye with ordinary dyes for PET, and thus cause problems in the coloring properties of dyed products and cause spotting. In addition, it has been found that since peeling occurs at the core-sheath interface after dyeing, sheath cracking and fibrillation easily occur due to friction, and there is a problem in abrasion resistance.
[0007]
[Problems to be solved by the invention]
The present invention has been obtained as a result of repeated studies in order to improve the productivity by increasing the discharge amount and to solve the problems of the coloring property, the spots of stain, and the abrasion resistance.
[0008]
In other words, it is an object of the present invention to solve the problems of the color developing property, dye spots, and abrasion resistance of the fibers generated when the PET is spun at a high speed.
[0009]
[Means for Solving the Problems]
An object of the present invention is to provide a polyester in which a sheath component is substantially composed of polyethylene terephthalate, a core component in which polyester having 5-sodium sulfoisophthalic acid copolymerized in an amount of 2 to 15 mol%, and a core component composite ratio of 1 to 15% by weight. % Of the core-sheath conjugate fiber at a spinning speed of 4000 to 12000 m / min.
[0010]
BEST MODE FOR CARRYING OUT THE INVENTION
Hereinafter, the present invention will be described in detail.
[0011]
PET in the sheath component may be one in which a part of the diol component and a part of the acid component are each substituted with another copolymerizable component in a range of 15 mol% or less. They may also contain additives such as matting agents, flame retardants, antistatic agents, pigments and the like.
[0012]
If the core component polymer is a polyester in which 5-sodium sulfoisophthalic acid is copolymerized in an amount of 2 to 15 mol%, both high spinning speed, dyeability and abrasion resistance can be achieved.
[0013]
The higher the copolymerization rate of 5-sodium sulfoisophthalic acid is, the higher the productivity improvement effect is preferable. However, if the copolymerization rate is excessively increased, a sharp increase in viscosity occurs in the polymerization process, and the polymerization degree of the polymer may be increased. The problem that it cannot be done arises. Further, the thermal stability of the polymer is also reduced, so that the spinnability is deteriorated. If the copolymerization ratio of 5-sodium sulfoisophthalic acid is 2 to 15 mol%, the spinnability is good. Preferably it is 5 to 12 mol%.
[0014]
The core component polymer may be copolymerized with isophthalic acid in addition to 5-sodium sulfoisophthalic acid as long as the present invention can be achieved.
[0015]
In the present invention, the copolymerization ratio of 5-sodium sulfoisophthalic acid means a molar ratio of 5-sodium sulfoisophthalic acid to all acid components in the polymer.
[0016]
The core component polymer may be a 5-sodium sulfoisophthalic acid copolymerized polyester alone, or may be a mixture with another polymer such as nylon as long as the effects of the present invention are exhibited.
[0017]
The shape of the core-sheath is not particularly limited, and may be a concentric core-sheath or an eccentric core-sheath, a shape having a plurality of cores, or a sea-island structure. That is, it is preferable that the core component polymer is continuously present in a constant amount in the fiber axis direction and is not exposed on the fiber surface. Therefore, the core polymer is preferably a concentric core-sheath collected at the center as much as possible from the viewpoints of coloring properties and abrasion resistance.
[0018]
When the 5-sodium sulfoisophthalic acid copolymerized polyester is on the sheath side, the sheath side is rapidly cooled in the high-speed spinning process, so that the adverse effect of the copolymerized polymer is likely to be manifested, and spinning malfunctions or defects such as microvoids in the obtained fiber are caused. , A large amount of steel is generated and the material becomes brittle, so that the effect of improving the residual elongation is not exhibited, and the strength is further reduced. The adverse effect of this quenching is not so significant in the case of low-speed spinning, but the effect increases rapidly as the spinning speed increases. It is described in "HIGH-SPEED FIBER SPINNING", p. 447 (WILEY-INTERSCIENCE) or the like that high-speed spinning reduces the fiber properties of even a homo-PET single yarn by rapid cooling. For this reason, special care must be taken when high-speed spinning is performed using a copolymerized polyester polymer as in the present invention. In particular, when the spinning speed is 6000 m / min or more, it is almost difficult to obtain practically usable fibers when the copolyester is used as a sheath. Actually, high-speed spinning using 5-sodium sulfoisophthalic acid copolymerized polyester as the sheath side is disclosed in JP-A-64-14333 and JP-A-5-9855. The effect of increasing the residual elongation of the obtained fiber is not only not recognized, but also the strength is low and it is difficult to use it as a filament for clothing or industrial material.
[0019]
If the fiber obtained by spinning has the property of a so-called highly oriented undrawn yarn (POY) having a residual elongation of 70% or more, it is preferable to further draw or draw false twist. Considering the processability and process stability at that time, it is considered that the obtained fiber should be oriented to some extent. Therefore, the spinning speed is preferably 4000 m / min or more.
[0020]
Usually, highly oriented undrawn yarn of PET for drawing false twisting is produced at a spinning speed of about 3000 m / min. Although drawing false twisting is not impossible even with a fiber obtained at a spinning speed of 4000 m / min, the residual elongation of the obtained processed yarn is excessively reduced, so that compared to a fiber obtained at a spinning speed of 3000 m / min. It is necessary to greatly reduce the draw ratio. Therefore, the overall productivity of spinning / drawing false twisting does not necessarily increase and is not preferable. In addition, when processing is performed with a high draw ratio to match the productivity, the tension of the twisted / untwisted portion is excessively increased, so that fluffing and yarn breakage are likely to occur, and the operability of the draw false twisting process is reduced. .
[0021]
In contrast, in the present invention, by arranging the 5-sodium sulfoisophthalic acid copolymerized polyester as the core of the specific amount of the conjugate fiber, the degree of orientation of the highly oriented undrawn yarn obtained even at a high spinning speed is suppressed, This improves the productivity of spinning / drawing false twisting.
[0022]
On the other hand, a fiber obtained by spinning and having a residual elongation of less than 70% can be used for clothing without any special stretching step. At this time, the spinning speed is preferably 8000 m / min or more from the viewpoint of productivity. ADVANTAGE OF THE INVENTION According to this invention, even if the spinning speed is 10000 m / min or more, the drop in the high elongation is small, and the fiber which can be practically used for clothing is not limited to the spinning speed of 8000 m / min, which was conventionally low in the strength and unpractical. Can be obtained. Then, the fiber obtained by the high-speed spinning can be subjected to false twisting.
[0023]
The above-described effect of suppressing the increase in the degree of orientation is 1% by weight or more, preferably 3% by weight or more, as a composite ratio of the core component depending on the purpose. If the core component composite ratio is less than 1% by weight, a sufficient orientation suppressing effect cannot be expected. On the other hand, as the core component composite ratio is increased, the effect of suppressing the orientation becomes remarkable. However, considering the strength of the final product, fiber cross-section deformation during false twisting, heat setting property, and the like, 15% by weight or less, preferably 10% by weight or less. % By weight or less.
[0024]
In the present invention, since a relatively small amount of the copolyester is disposed on the core, troubles such as fusion do not occur even when high-temperature heat treatment is performed. In addition, since it has high compatibility with the sheath component PET, there is no occurrence of peeling at the core / sheath interface, and the wear resistance is good. Further, the core component has higher dyeability than the sheath component, and not only improves the color development, but also improves the discoloration characteristics (frosting characteristics) due to friction.
[0025]
5-Sodium sulfoisophthalic acid is a very well-known polymer for modifying PET. The copolymer is widely used for the purpose of improving dyeability, alkali elution property and the like. However, in the case of composite fibers, 5-sodium sulfoisophthalic acid copolymerized polyester is mostly used for the sheath portion in order to impart functionality to the fiber, and as in the present invention, 5-sodium sulfoisophthalic acid copolymerized polyester is used. The effect of suppressing the orientation of the PET fiber only by compounding a specific amount was not known at all.
[0026]
As described above, it is not clear why the 5-sodium sulfoisophthalic acid copolymerized polyester suppresses the orientation of PET by high-speed spinning and increases the residual elongation of the obtained fiber. It is thought that this influences the thinning behavior and reduces the internal stress when the oriented structure of the sheath PET is formed, thereby suppressing the orientation of the PET.
[0027]
According to the present invention, even at a high speed spinning of 4000 to 6000 m / min, the obtained fiber can be drawn (false twisted) at a draw ratio of 1.2 to 2.0 times, and is superior in productivity to the conventional one. It is a manufacturing method. Further, in the high-speed spinning of PET alone, the fiber obtained at a spinning speed of 8000 m / min or more is inferior in the high elongation characteristic, whereas in the method of the present invention, the practical high elongation characteristic is obtained even at the spinning speed of 8000 m / min or more. This is a production method which is superior in productivity to the conventional one even in ultra high speed spinning.
[0028]
The polyester fiber obtained by the present invention, as raw silk, or as a twisted yarn or false twisted yarn, is used for clothing such as lining, sportswear, slacks, blousons, blouses, and for materials such as ribbons, tapes and belts. It can be suitably used.
[0029]
【Example】
Hereinafter, the present invention will be described in detail with reference to examples.
[0030]
In addition, the following method was used for the measuring method in an Example.
[0031]
A. Intrinsic viscosity [η]
Measured in orthochlorophenol at 25 ° C.
[0032]
B. Stress-elongation curve, strength and elongation A load-elongation curve was determined according to JIS L1013.
[0033]
Next, the load value was divided by the initial fineness, which was taken as stress (strength), the elongation was divided by the initial sample length, and a stress-elongation curve consisting of strength and elongation was obtained.
[0034]
C. After the dyed fiber was knitted in a tube, the dyed fiber was dyed with Terrasil Navy Blue SGL, and the color development and the sensory evaluation of spots were performed.
[0035]
D. The knitted fabric after knitting, dyeing and rubbing the abrasion resistant fibers was subjected to a sensory evaluation.
[0036]
Example 1
A homopolyester having an intrinsic viscosity of 0.63 and a copolymerized polyester having an intrinsic viscosity of 0.63 obtained by copolymerizing 12 mol% of 5-sodium sulfoisophthalic acid are separately melted, and filtered through a stainless steel nonwoven filter having an absolute filtration diameter of 5 μm. Then, a copolyester core and a homo-PET core / sheath composite on a concentric sheath were discharged from a die having a hole diameter of 0.25 mm and 36 holes. At this time, the composite ratio of the core component was 8% by weight. The spinning temperature was adjusted to 295 ° C., and the discharge rate was adjusted to a single yarn fineness of 4 dtex. The discharged yarn was cooled by a conventional method after discharge, lubricated after refueling, and wound up by a winding machine via a take-off roller. The peripheral speed of the take-off roller that the yarn first touches is shown in Table 1 as the spinning speed (Experiment Nos. 1 to 5). At this time, the stress-elongation curves of the fibers obtained at spinning speeds of 6000 m / min and 10000 m / min are shown in curve A of FIG. 1 and curve A of FIG. 2, respectively. Table 1 shows the strength and elongation. FIG. 1 and FIG. The results for the 10 and 12 uncopolymerized PET-only yarns are shown as curve B, respectively.
[0037]
Even at a spinning speed of 6000 m / min (FIG. 1A), unlike the case of PET alone (Comparative Example 1, FIG. 1B), the conjugate fiber of the present invention has a constant stress extension region and is an undrawn yarn. Furthermore, even at a spinning speed of 10000 m / min (FIG. 2A), it can be seen that unlike the case of PET alone (Comparative Example 1, FIG. 2B), it has good high elongation characteristics. Further, as can be seen from Table 1, when 5-sodium sulfoisophthalic acid copolymerized polyester was combined with homo-PET, the effect of improving elongation over the entire spinning speed region as compared with PET alone yarn (Experiment Nos. 9 to 13). was gotten.
[0038]
The fibers obtained at spinning speeds of 4000 and 6000 m / min were subjected to draw false twisting at a heater temperature of 220 ° C. and draw ratios of 1.95 and 1.68, respectively. Table 2 shows the coloring properties, spots and abrasion resistance of the stretched false twisted fiber and the fiber itself obtained at a spinning speed of 8000 to 12000 m / min. Both the drawn false twisted fiber and the ultrahigh-speed spun fiber having a spinning speed of 8000 m / min or more had good color developability, spotted spots and abrasion resistance.
[0039]
Example 2
Melt spinning was carried out under the same conditions as in Example 1 (Experiment No. 2) except that the copolymerized polyester was changed to 5-sodium sulfoisophthalic acid 6 mol% copolymer (intrinsic viscosity 0.65) (Experiment No. 6). ). Table 1 shows the strength and elongation. At this time, the elongation improvement effect was also observed. Further, at a heater temperature of 220 ° C. and a draw ratio of 1.32 times, the fiber was subjected to draw false twisting. The color development, dyeing spots and abrasion resistance of the drawn false twisted fiber were also good (Table 2).
[0040]
Example 3
Melt spinning was performed (Experiment No. 7) under the same conditions as in Example 1 (Experiment No. 2) except that the copolymerized polyester was changed to 5-sodium sulfoisophthalic acid 2 mol% copolymer (intrinsic viscosity: 0.65). Table 1 shows the strength and elongation. At this time, the effect of improving the elongation is small, but it can be seen that the strength is improved as compared with that of Example 1 having the same spinning speed. In addition, this fiber was subjected to draw false twisting at a heater temperature of 220 ° C. and a draw ratio of 1.22 times. The color development, dyeing spots and abrasion resistance of the drawn false twisted fiber were also good (Table 2).
[0041]
Example 4
Spinning was carried out under the same conditions as in Example 1 (Experiment No. 2) except that the copolymerization ratio of 5-sodium sulfoisophthalic acid was changed to 10 mol%, and isophthalic acid was further copolymerized to 20 mol (intrinsic viscosity: 0.60). (Experiment No. 8). Table 1 shows the strength and elongation. At this time, the elongation improvement effect was also observed. In addition, drawing false twisting of this fiber was performed at a heater temperature of 220 ° C. and a draw ratio of 1.60. The color development, dyeing spots and abrasion resistance of the drawn false twisted fiber were also good (Table 2).
[0042]
Comparative Example 1
The polymer was only the homo-PET used in Example 1, and the single yarn was melt-spun under the same conditions as in Example 1 without using composite spinning (Experiments Nos. 9 to 13). The strength and elongation are shown in Table 1.
[0043]
The stress-elongation curves of the fibers obtained at spinning speeds of 6000 m / min and 10000 m / min are shown in curve B of FIG. 1 and curve B of FIG. 2, respectively. Both show typical characteristics of PET fibers, and it can be seen that at a spinning speed of 6000 m / min, stretching has already occurred up to winding and has no constant stress elongation region and is not an undrawn yarn.
[0044]
At a spinning speed of 10,000 m / min, unlike the case of 12 mol% of 5-sodium sulfoisophthalic acid copolymerized polyester composite, it has a high elongation characteristic that does not endure practical use. In addition, although the fiber obtained at a heater temperature of 220 ° C. and a draw ratio of 1.32 times at a spinning speed of 4000 m / min was subjected to drawing false twisting, fluffing occurred frequently during processing. Table 2 shows the coloring properties, spots of stain, and abrasion resistance of the drawn false twisted fibers.
[0045]
Example 5
Melt spinning was performed under the same conditions as in Example 1 (No. 2) except that the composite ratio of the copolymerized polyester was 5 and 14% by weight (Experiment Nos. 14 and 15). Table 1 shows the strength and elongation. It can be seen that the larger the composite ratio, the greater the elongation improvement effect. Further, at a heater temperature of 220 ° C., a 5% by weight composite fiber was subjected to draw false twisting at a draw ratio of 1.32 times, and a 14% by weight composite fiber at a draw ratio of 1.94 times.
[0046]
The color development, dyeing spots and abrasion resistance of the drawn false twisted fiber were also good (Table 2).
[0047]
Comparative Example 2
Spinning was performed under the same conditions as in Example 1 (Experiment No. 2) except that the copolymerization ratio of 5-sodium sulfoisophthalic acid was set to 1 (intrinsic viscosity 0.65) and 17 mol% (intrinsic viscosity 0.57). (Experiment Nos. 16 and 17). The strength and elongation are shown in Table 1. At a copolymerization ratio of 1 mol%, the elongation improving effect was hardly observed. At a copolymerization rate of 17 mol%, the effect of improving elongation was large, but the spinning condition was poor and the number of yarn breaks occurred frequently, and the strength of the obtained fiber was also low.
[0048]
Comparative Example 3
Spinning was performed under the same conditions as in Example 2 (Experiment No. 6) except that the composite ratio of the copolymerized polyester was changed to 18% by weight (Experiment No. 18). The strength and elongation are shown in Table 1. Although the elongation improvement effect was great, the spinning condition was slightly poor. This fiber was subjected to draw false twisting at a heater temperature of 220 ° C. and a factor of 1.95. However, fluffing occurred frequently during processing, and the coloring property, spots of staining, and abrasion resistance were poor (Table 2). Further, the strength of the drawn false twisted yarn was excessively reduced, and the cross-sectional deformation was too large. There were also disadvantages such as.
[0049]
Comparative Example 4
Melt spinning was carried out under the same conditions as in Example 3 except that the core polymer and the sheath polymer of Example 3 were replaced and the sheath polymer (2-sodium sulfoisophthalic acid 2 mol% copolymerization) composite ratio was 10% by weight. (Experiment No. 19). At this time, not only the elongation was hardly improved but also the strength was significantly reduced (Table 1). Further, the spinning was abnormal, and the yarn was frequently broken.
[0050]
Comparative Example 5
Melt spinning was performed at a spinning speed of 6000 m / min under the same conditions as in Example 1 except that the core polymer of Example 1 (12 mol% of 5-sodium sulfoisophthalic acid copolymer) was not a composite but a blend. No. 20). At this time, a slight elongation improvement effect was observed, but the spinning was abnormal, and the yarn was frequently broken.
[0051]
[Table 1]
Figure 0003570171
[Table 2]
Figure 0003570171
[0052]
【The invention's effect】
By employing the method for producing the core-sheath conjugate fiber of the present invention, the discharge amount per unit time can be greatly increased, and the drawbacks of the prior art such as coloring property and abrasion resistance can be overcome. . In other words, the present invention can solve the problems of the color developing property, spots of staining, and abrasion resistance of the fiber which occur when spinning polyethylene terephthalate at a high speed.
[Brief description of the drawings]
FIG. 1 is a view showing a stress-elongation curve of a fiber obtained by spinning at a spinning speed of 6000 m / min in Examples and Comparative Examples of the present invention.
FIG. 2 is a view showing a stress-elongation curve of a fiber obtained by spinning at a spinning speed of 10,000 m / min in Examples and Comparative Examples of the present invention.
[Explanation of symbols]
A core-sheath composite fiber B having 5-sodium sulfoisophthalic acid copolymerized polyester core and homo PET sheath B PET single fiber

Claims (2)

鞘成分が実質的にポリエチレンテレフタレートからなるポリエステル、芯成分が5−ナトリウムスルホイソフタル酸が2〜15モル%共重合されたポリエステルからなり、芯成分複合比が1〜15重量%である芯鞘複合繊維を紡糸速度4000〜12000m/分で紡糸することを特徴とする芯鞘複合繊維の製造法。A core-sheath composite in which the sheath component is substantially composed of polyethylene terephthalate, and the core component is a polyester in which 5-sodium sulfoisophthalic acid is copolymerized with 2 to 15 mol%, and the core component composite ratio is 1 to 15% by weight. A method for producing a core-sheath composite fiber, comprising spinning the fiber at a spinning speed of 4000 to 12000 m / min. 請求項1記載の製造方法で得られた繊維に仮撚加工を施すことを特徴とする芯鞘複合繊維からなる仮撚加工糸の製造法の製造法。A method for producing a false twisted yarn comprising a core-sheath composite fiber, wherein the fiber obtained by the production method according to claim 1 is subjected to false twisting.
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