JPH0770827A - Polyester 3-component composite fiber - Google Patents

Polyester 3-component composite fiber

Info

Publication number
JPH0770827A
JPH0770827A JP6102906A JP10290694A JPH0770827A JP H0770827 A JPH0770827 A JP H0770827A JP 6102906 A JP6102906 A JP 6102906A JP 10290694 A JP10290694 A JP 10290694A JP H0770827 A JPH0770827 A JP H0770827A
Authority
JP
Japan
Prior art keywords
component
sea
island
fiber
strength
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
JP6102906A
Other languages
Japanese (ja)
Inventor
Masayuki Sato
正幸 佐藤
Yoshihiro Konno
吉宏 近野
Hiroshi Takahashi
洋 高橋
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP6102906A priority Critical patent/JPH0770827A/en
Publication of JPH0770827A publication Critical patent/JPH0770827A/en
Pending legal-status Critical Current

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  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Artificial Filaments (AREA)
  • Multicomponent Fibers (AREA)

Abstract

(57)【要約】 【構成】 芯成分A、島成分B、海成分Cのいずれも相
異なる3種のポリエステルからなり、島成分Bが芯成分
Aを取り囲むように点在し、且つ海成分Cのなかに偏在
することなく分散してなる3成分複合繊維において、海
成分Cの溶融粘度に対する芯成分Aおよび島成分Bの溶
融粘度の比、および原糸強度に対する海成分溶解除去後
の繊維強度の比を特定化したポリエステル系3成分複合
繊維。 【効果】 本発明により、張り・腰とソフトタッチな風
合、ふくらみ感をかね備えた新規な風合を有する布帛を
得るためのポリエステル系3成分複合繊維において、複
合形態の安定性および工程通過性、実用特性の優れた複
合繊維を得ることができる。
(57) [Summary] [Structure] The core component A, the island component B, and the sea component C are all composed of three different polyesters, and the island components B are scattered so as to surround the core component A, and the sea component In a three-component composite fiber dispersed in C without being unevenly distributed, the ratio of the melt viscosity of the core component A and the island component B to the melt viscosity of the sea component C, and the fiber after the sea component is dissolved and removed with respect to the yarn strength. A polyester-based three-component composite fiber with a specified strength ratio. [Effect] According to the present invention, in a polyester-based three-component conjugate fiber for obtaining a fabric having a novel texture having a soft touch and a feeling of swelling and softness, stability of the composite form and passage through the process It is possible to obtain a composite fiber having excellent properties and practical properties.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、衣料用ポリエステル系
3成分複合繊維に関する。さらに詳しくは、複合形態の
安定性に優れ、且つ高強力である衣料用ポリエステル系
3成分複合繊維に関する。
TECHNICAL FIELD The present invention relates to a polyester-based three-component composite fiber for clothing. More specifically, the present invention relates to a polyester-based three-component conjugate fiber for clothing, which has excellent stability in a composite form and high strength.

【0002】[0002]

【従来の技術】近年、衣料用布帛は、ニーズの多様化、
高級化の要求が高まっており、種々の検討がなされてい
る。その一つとして、3成分系複合紡糸技術による検討
がなされている。例えば、特開平1−14321号公報
では、高収縮な芯成分、低収縮な島成分、易アルカリ減
量性の海成分からなるポリエステル系3成分複合繊維に
よって、張り・腰とソフトタッチな風合をかね備えた新
規な風合が得られることが開示されている。しかしなが
ら、該公報で用いている海成分ポリマの溶融粘度は、芯
成分および島成分の溶融粘度に比較して非常に高く、複
合形態の安定性は非常に良好であるが、得られる原糸の
強度、更には海成分溶解除去後の繊維の強度は低く、布
帛の引裂強力の低下や摩耗によるフィブリル化の発生な
どの実用特性面での問題が生じ、展開用途が限定されて
いた。また、特開平2−26912号公報においても、
高収縮な芯成分、低収縮な島成分、易アルカリ減量性の
海成分からなる3成分複合繊維によって、張り・腰とソ
フトタッチな風合をかね備えた新規な風合が得られるこ
とが開示されている。しかしながら、該公報の技術を用
いても、前記特開平1−14321号公報と同様の問題
が発生することがわかった。
2. Description of the Related Art In recent years, clothing fabrics have diversified needs,
The demand for higher quality is increasing, and various studies have been made. As one of them, studies have been made using a three-component composite spinning technique. For example, in JP-A-1-14321, a polyester-based three-component composite fiber composed of a highly-shrinkable core component, a low-shrinkage island component, and an easily alkali-reducing sea component provides a soft touch with tightness and waist. It is disclosed that a new texture with a texture is obtained. However, the melt viscosity of the sea component polymer used in this publication is very high as compared with the melt viscosities of the core component and the island component, and the stability of the composite form is very good. The strength, and further the strength of the fiber after the sea component is dissolved and removed, are low, and problems in practical properties such as a decrease in tear strength of the fabric and occurrence of fibrillation due to abrasion occur, and thus the application range is limited. Further, in Japanese Patent Laid-Open No. 2-26912,
It is disclosed that a new texture with softness and softness can be obtained by using a three-component composite fiber consisting of a highly shrinkable core component, a low shrinkage island component, and an alkali-reducing sea component. Has been done. However, it has been found that even when the technique of this publication is used, the same problem as in the above-mentioned JP-A-1-14321 occurs.

【0003】また、熱水可溶性ポリエステルについても
種々の検討がなされており、例えば、特公昭64−62
86号公報では、海島型複合繊維の一成分として5−ナ
トリウムスルホイソフタル酸およびイソフタル酸を共重
合した熱水可溶性ポリエステルを用いた複合繊維につい
て開示されている。しかしながら該公報では、単に2成
分複合繊維について記載されているに過ぎず、本発明の
如き異繊度、異収縮成分と海成分からなる3成分複合繊
維については何等開示されていない。従って、異繊度、
異収縮性の特徴をより効果的に発揮し、目的とする張り
・腰とソフトタッチな風合をかね備えた新規な風合を有
する布帛を得ることはできなかった。また、島成分ポリ
マと海成分ポリマの溶融粘度の比によっては複合形態の
異常による製糸性不良を招いたり、あるいは海成分溶解
除去後の繊維強度の低下により実用特性面で問題が発生
することがわかった。
Various studies have been made on hot water-soluble polyesters, for example, Japanese Patent Publication No. 64-62.
Japanese Patent Publication No. 86 discloses a composite fiber using a hot water-soluble polyester obtained by copolymerizing 5-sodium sulfoisophthalic acid and isophthalic acid as one component of the sea-island type composite fiber. However, this publication merely describes a two-component composite fiber, and does not disclose any three-component composite fiber having different fineness, different shrinkage component and sea component as in the present invention. Therefore, the degree of heterogeneity,
It has not been possible to obtain a fabric having a novel texture that exhibits the characteristic of different shrinkage more effectively and has a desired tension / waist and soft touch. Also, depending on the ratio of the melt viscosity of the island component polymer and the sea component polymer, it may lead to poor spinnability due to abnormalities in the composite form, or a problem in terms of practical properties may occur due to the decrease in fiber strength after dissolution and removal of the sea component. all right.

【0004】[0004]

【発明が解決しようとする課題】本発明の目的は、張り
・腰とソフトタッチな風合をかね備えた新規な風合を有
する布帛を得るためのポリエステル系3成分複合繊維に
おいて、操業安定性、即ち複合形態安定性にすぐれ、且
つ実用上問題の発生しないポリエステル系3成分複合繊
維を提供することにある。
SUMMARY OF THE INVENTION An object of the present invention is to provide a polyester-based three-component composite fiber for obtaining a fabric having a novel texture having a soft feeling and a soft feel, and stability in operation. That is, it is to provide a polyester-based three-component conjugate fiber which is excellent in composite morphological stability and causes no practical problems.

【0005】[0005]

【課題を解決するための手段】このような本発明の目的
は、芯成分A、島成分B、海成分Cのいずれも相異なる
3種のポリエステルからなり、島成分Bが芯成分Aを取
り囲むように点在し、且つ海成分Cのなかに偏在するこ
となく分散してなる3成分複合繊維において、海成分C
の溶融粘度(εc)に対する芯成分Aおよび島成分Bの
溶融粘度(εaおよびεb)の比、εa/εcおよびε
b/εcが、いずれも0.80以上、2.50以下であ
り、原糸強度(T1)に対する海成分溶解除去後の繊維
強度(T2)の比、T2/T1が1.02以上であるポ
リエステル系3成分複合繊維(以下、複合繊維という)
によって達成できる。
The object of the present invention is such that the core component A, the island component B, and the sea component C are composed of three different polyesters, and the island component B surrounds the core component A. In the three-component composite fiber which is dispersed in the sea component C without being unevenly distributed, the sea component C
Of melt viscosity (εa and εb) of core component A and island component B to melt viscosity (εc) of ε, εa / εc and ε
b / εc are both 0.80 or more and 2.50 or less, and T2 / T1 is 1.02 or more, which is the ratio of the fiber strength (T2) after the sea component is dissolved and removed to the raw yarn strength (T1). Polyester 3-component composite fiber (hereinafter referred to as composite fiber)
Can be achieved by

【0006】図1は本発明の複合繊維の一例を示す複合
断面図である。Aは芯成分Aであり、Bは島成分Bであ
り、Cは海成分Cである。個々の島成分Bは海成分C中
に偏在することなく存在していることが必要である。す
なわち、個々の島成分Bは海成分Cにより分離されてい
ると共に、芯成分Aとも海成分Cにより分離されている
ことが好ましい。芯成分Aと個々の島成分B、および個
々の島成分B同志が海成分Cにより分離されていない
と、海成分Cを溶解除去しても、芯成分Aと個々の島成
分Bおよび個々の島成分B同志を分離することができ
ず、目的とするソフトタッチな風合を十分に得ることが
できない。
FIG. 1 is a composite sectional view showing an example of the composite fiber of the present invention. A is the core component A, B is the island component B, and C is the sea component C. It is necessary that the individual island component B exists in the sea component C without being unevenly distributed. That is, it is preferable that the individual island component B is separated by the sea component C, and the core component A is also separated by the sea component C. If the core component A and the individual island component B and the individual island component B are not separated by the sea component C, even if the sea component C is dissolved and removed, the core component A, the individual island component B and the individual island component B are separated. The island components B cannot be separated from each other, and the desired soft-touch texture cannot be obtained sufficiently.

【0007】本発明では、海成分Cに対する芯成分Aお
よび島成分Bの溶融粘度の比では、紡糸における複合形
態の安定性と、得られる原糸の強度、更には海成分溶解
除去後の繊維の強度に密接な関係を有しており、該溶融
粘度比を特定の範囲とすることによって、複合形態を安
定化し、且つ高次加工、および実用の上で十分な強度を
有する原糸を得ることができるのである。即ち、海成分
Cに対する芯成分Aおよび島成分Bの溶融粘度の比、ε
a/εcおよびεb/εcが、いずれも0.80以上、
2.50以下であることが必要である。εa/εcまた
はεb/εcが0.80未満の場合、海成分Cの溶融粘
度が高すぎるため、複合形態の安定性の面からは安定し
た複合形態を得ることができるが、原糸強度、更には海
成分溶解除去後の繊維の強度の低下が著しく、高次加工
工程の通過性が悪化すると共に、布帛とした際に引裂強
力が低く、また摩耗によるフィブリル化が起こり、実用
上の問題が生じるのである。逆に、εa/εcまたはε
b/εcが2.50を越えると、海成分Cの溶融粘度が
低すぎて、安定した複合形態を得ることが困難となるた
め、製糸性が不良となり操業安定性が著しく損われてし
まうのである。前述の原糸および海成分溶解除去後の繊
維の強度の低下は、以下のようなメカニズムによって生
じるものと考えられる。即ち、海成分の溶融粘度が芯成
分および島成分に比較して非常に高いため、紡糸時の紡
糸応力が海成分に集中し、紡糸段階において海成分の繊
維構造の形成が優先的に進行し、逆に芯成分および島成
分は紡糸応力が余りかからないため、繊維構造の形成が
十分に行なわれない。即ち、海成分の構造は紡糸速度よ
り高紡速で紡糸した構造となり、逆に芯成分および島成
分は低紡速で紡糸した構造となる。従って、その後に行
なう延伸では、最も延伸性の低い海成分によって延伸倍
率が決定され、芯成分および島成分が十分に延伸されず
に延伸が完了することとなり、得られる原糸の強度、更
には海成分溶解除去後の繊維の強度が低下する。紡糸に
おける複合形態を安定化し、且つ高次加工、および実用
の上で十分な原糸強度を得るための、海成分Cに対する
芯成分Aおよび島成分Bの溶融粘度の比、εa/εcお
よびεb/εcの範囲は、好ましくは0.80以上、
2.00以下であり、より好ましくは0.80以上1.
80以下である。なお、溶融粘度の測定は、東洋精機製
作所(株)製キャピログラフ1Bにより、290℃、ず
り速度1200(1/秒)において測定した値である。
In the present invention, the ratio of the melt viscosities of the core component A and the island component B to the sea component C, the stability of the composite form in spinning, the strength of the obtained raw yarn, and further the fiber after the sea component is dissolved and removed. Has a close relationship with the strength of the fiber, and by setting the melt viscosity ratio within a specific range, a composite morphology is stabilized, and a yarn having sufficient strength for high-order processing and practical use is obtained. It is possible. That is, the ratio of the melt viscosity of the core component A and the island component B to the sea component C, ε
a / εc and εb / εc are both 0.80 or more,
It should be 2.50 or less. When εa / εc or εb / εc is less than 0.80, since the melt viscosity of the sea component C is too high, a stable composite form can be obtained from the aspect of stability of the composite form, but the raw yarn strength, Furthermore, the strength of the fiber after the sea component is dissolved and removed is remarkably reduced, the passability in the higher-order processing step is deteriorated, the tear strength is low when the fabric is formed, and fibrillation due to abrasion occurs, which is a practical problem. Occurs. Conversely, εa / εc or ε
If b / εc exceeds 2.50, the melt viscosity of the sea component C will be too low, and it will be difficult to obtain a stable composite form, resulting in poor spinnability and markedly impaired operational stability. is there. The decrease in the strength of the fiber after the dissolution of the raw yarn and the sea component is considered to be caused by the following mechanism. That is, since the melt viscosity of the sea component is much higher than that of the core component and the island component, the spinning stress during spinning concentrates on the sea component, and the formation of the fiber structure of the sea component preferentially progresses at the spinning stage. On the contrary, since the core component and the island component do not apply the spinning stress so much, the fiber structure is not sufficiently formed. That is, the structure of the sea component becomes a structure spun at a higher spinning speed than the spinning speed, and conversely, the core component and the island component become a structure spun at a low spinning speed. Therefore, in the subsequent drawing, the draw ratio is determined by the sea component having the lowest drawability, the drawing is completed without the core component and the island component being sufficiently drawn, and the strength of the obtained raw yarn, and further The strength of the fiber after the dissolution and removal of the sea component decreases. Ratio of melt viscosity of the core component A and the island component B to the sea component C, εa / εc and εb, for stabilizing the composite morphology in spinning and obtaining sufficient yarn strength for higher-order processing and practical use. The range of / εc is preferably 0.80 or more,
2.00 or less, and more preferably 0.80 or more and 1.
It is 80 or less. The melt viscosity is a value measured by Capillograph 1B manufactured by Toyo Seiki Seisaku-sho, Ltd. at 290 ° C. and a shear rate of 1200 (1 / sec).

【0008】本発明の複合繊維は、原糸強度(T1)に
対する海成分溶解除去後の繊維強度(T2)の比、T2
/T1が1.02以上であることが必要である。T2/
T1の比が1.02未満であると、海成分溶解除去工
程、例えばアルカリ熱水処理において、非溶解成分、即
ち芯成分Aおよび島成分Bの加水分解などによる劣化が
進行し、布帛とした際の引裂強力が低く、また摩耗によ
るフィブリル化が起こり、実用上の問題が発生するた
め、製品の耐久性や毛羽発生等による品位の低下が起こ
る。T2/T1の比は、好ましくは1.05以上であ
る。なお、海成分溶解除去後の繊維強度の測定は以下の
方法で行なう。複合繊維を定長で100℃以下の処理温
度で脱海した後、通常の方法で強伸度を測定し、海成分
溶解除去後の繊維の繊度を下記式より計算し強度を求め
る。◎ 繊度=原糸繊度×(芯成分複合比+島成分複合比)
The composite fiber of the present invention has a ratio of the fiber strength (T2) after the sea component is dissolved and removed to the raw fiber strength (T1), T2.
It is necessary that / T1 is 1.02 or more. T2 /
When the ratio of T1 is less than 1.02, in the sea component dissolving / removing step, for example, the alkaline hot water treatment, the non-dissolved components, that is, the core component A and the island component B are deteriorated due to hydrolysis and the like, and the fabric is obtained. At that time, the tear strength is low, and fibrillation occurs due to abrasion, which causes a problem in practical use, resulting in deterioration of product durability and generation of fluff, thus degrading quality. The ratio of T2 / T1 is preferably 1.05 or more. The measurement of the fiber strength after dissolution and removal of sea components is carried out by the following method. After the sea length of the composite fiber is removed at a treatment temperature of 100 ° C. or less, the strength and elongation are measured by a usual method, and the fineness of the fiber after dissolution and removal of sea components is calculated from the following formula to obtain the strength. ◎ Fineness = Raw yarn fineness x (Core component composite ratio + Island component composite ratio)

【0009】本発明の複合繊維は、該繊維を用いて布帛
とした後、例えば熱水やアルカリ熱水溶液で海成分Cを
溶解除去し、芯成分Aと島成分Bとに分離することによ
って独特の風合を得るものである。本発明の複合繊維
は、風合面、特に張り・腰の点で複合フィラメントを構
成する芯成分Aの繊度は、1.0デニール以上5.0デ
ニール以下であることが好ましい。芯成分Aの繊度が
1.0デニール未満であると、布帛に十分な張り・腰を
付与することができず、逆に5.0デニールを越えると
硬い風合となる。
The composite fiber of the present invention is unique in that after the fabric is formed from the fiber, the sea component C is dissolved and removed with, for example, hot water or an alkali hot aqueous solution, and the core component A and the island component B are separated. It is what you get. In the conjugate fiber of the present invention, the fineness of the core component A constituting the conjugate filament is preferably 1.0 denier or more and 5.0 denier or less in terms of texture surface, particularly tension / waist. If the fineness of the core component A is less than 1.0 denier, it is not possible to impart sufficient tension and stiffness to the fabric, and conversely, if it exceeds 5.0 denier, the fabric has a hard texture.

【0010】また、ソフトタッチな風合という点で、複
合繊維を構成する島成分Bの繊度は、0.1デニール以
上0.6デニール以下が好ましい。島成分Bの繊度が
0.1デニール未満ではソフトタッチな風合が得られる
ものの、布帛の柔軟さが強調され過ぎてしまい、逆に
0.6デニールを越えるとソフトタッチな風合を得るこ
とができない。また、島成分Bの形状については、特に
限定しないが円形、楕円形、偏平形が好ましく、特に偏
平形が好ましい。島成分Bの形状を偏平形とすることに
より、独特の表面タッチを表現することが可能となる。
島成分Bの形状を偏平形とする場合には、その偏平度を
1.5以上、5.0以下とすることが好ましい。偏平度
が1.5未満であると偏平化による独特の表面タッチを
得るには不十分であり、逆に偏平度が5.0を越える
と、島成分の厚みが薄くなることにより、偏平面に対す
る曲げ剛性が低下し、ふくらみ感が低下すると共に、極
細糸によるピーチタッチを得にくくなる傾向がある。な
お、本発明でいう偏平度とは、図1に示した複合断面図
において、繊維円周方向の島成分の最大長さL1と繊維
半径方向の島成分の最大長さL2との比L1/L2であ
る。島成分Bの複合繊維における存在個数は、風合面よ
り4個以上20個以下であることが好ましく、より好ま
しくは5個以上15個以下である。島成分Bの個数が3
個以下の場合、太繊度の芯成分Aの効果が強調されすぎ
硬い風合となり、島成分Bの個数が21個以上の場合、
極細繊度の島成分Bの効果が強調されすぎ柔らか過ぎる
風合となる。
From the viewpoint of soft touch, the fineness of the island component B constituting the composite fiber is preferably 0.1 denier or more and 0.6 denier or less. When the fineness of the island component B is less than 0.1 denier, a soft touch feeling can be obtained, but the softness of the fabric is too emphasized. Conversely, when it exceeds 0.6 denier, a soft touch feeling is obtained. I can't. The shape of the island component B is not particularly limited, but a circle, an ellipse, and a flat shape are preferable, and a flat shape is particularly preferable. By making the shape of the island component B flat, it is possible to express a unique surface touch.
When the island component B has a flat shape, the flatness is preferably 1.5 or more and 5.0 or less. If the flatness is less than 1.5, it is insufficient to obtain a unique surface touch due to flattening. On the contrary, if the flatness exceeds 5.0, the island component becomes thin, resulting in a flat surface. The bending rigidity with respect to the swelling decreases, the swelling feeling decreases, and it becomes difficult to obtain a peach touch with an ultrafine thread. The flatness referred to in the present invention is the ratio L1 / of the maximum length L1 of the island component in the fiber circumferential direction and the maximum length L2 of the island component in the fiber radial direction in the composite cross-sectional view shown in FIG. It is L2. The number of the island component B present in the composite fiber is preferably 4 or more and 20 or less, more preferably 5 or more and 15 or less, from the feeling surface. The number of island components B is 3
When the number of the island components B is 21 or more, the effect of the core component A having a large fineness is too emphasized, resulting in a hard texture, and when the number of the island components B is 21 or more,
The effect of the island component B having an extra fineness is emphasized too much and the texture becomes too soft.

【0011】本発明の複合繊維は、得られる布帛の風
合、品位の点で相異なる3種のポリマで形成されている
ことが必要であり、相異なる3種のポリマとは、製糸、
製編織する際に複合成分間で剥離を生じないように、相
溶性が良好なポリマを組み合わせることが必要である。
製編織する際に、複合成分間で剥離を生じると、毛羽、
たるみ、糸切れが発生しやすく工程通過性、製品品位の
点で問題が生じる。芯成分Aを構成するポリマの好まし
い例としては、アジピン酸、セバシン酸、イソフタル
酸、ジフェニルジカンボン酸、ナフタリンジカルボン酸
等の二塩基酸類、オキシ安息香酸の如きオキシ酸類、お
よびジエチレングリコール、プロピレングリコール、ポ
リエチレングリコール等のグリコール類、5−ナトリウ
ムスルホイソフタル酸、2,2ビス{4−(2−ヒドロ
キシエトキシ)フェニル}プロパンなどのうちから1種
または2種以上のものを共重合したポリエステルが挙げ
られるがこの限りではない。本発明で用いる芯成分Aと
しては、島成分Bによるピーチタッチ効果を増大し、且
つ布帛とした場合にふくらみ感を付与するという点か
ら、島成分Bより乾熱収縮率で5%以上高収縮であるこ
とが好ましい。なお、乾熱収縮率の測定は以下の方法で
行なう。複合繊維の脱海前の糸長L0 を測定し、100
℃以下の処理温度で脱海した後、200℃乾熱処理を1
5分行なう。次いで芯成分と島成分とを分離し糸長を測
定し、芯成分の糸長をLH 、島成分の糸長をLL とす
る。乾熱収縮率は次式により求める。 芯成分の乾熱収縮率(%)=(L0 −LH )/L0 ×1
00 島成分の乾熱収縮率(%)=(L0 −LL )/L0 ×1
00
The conjugate fiber of the present invention is required to be formed of three kinds of polymers which are different from each other in terms of feel and quality of the obtained cloth.
It is necessary to combine polymers having good compatibility so as not to cause separation between the composite components during knitting and weaving.
When peeling occurs between composite components during knitting or weaving, fluff,
Looseness and yarn breakage easily occur, which causes problems in terms of processability and product quality. Preferred examples of the polymer constituting the core component A include dibasic acids such as adipic acid, sebacic acid, isophthalic acid, diphenyldicambonic acid and naphthalene dicarboxylic acid, oxyacids such as oxybenzoic acid, and diethylene glycol, propylene glycol, Polyesters obtained by copolymerizing one kind or two or more kinds of glycols such as polyethylene glycol, 5-sodium sulfoisophthalic acid, 2,2 bis {4- (2-hydroxyethoxy) phenyl} propane and the like can be mentioned. But this is not the case. As the core component A used in the present invention, the peach touch effect by the island component B is increased, and a swelling feeling is imparted when the fabric is formed. Is preferred. The dry heat shrinkage is measured by the following method. The yarn length L0 of the composite fiber before sea removal was measured and 100
After de-sealing at a processing temperature of ℃ or less, dry heat treatment at 200 ℃ 1
Do 5 minutes. Next, the core component and the island component are separated and the yarn length is measured. The core component yarn length is LH and the island component yarn length is LL. The dry heat shrinkage is calculated by the following formula. Dry heat shrinkage of core component (%) = (L0-LH) / L0 × 1
00 Dry heat shrinkage (%) of island component = (L0-LL) / L0 x 1
00

【0012】島成分Bとしては、芯成分Aとの収縮率差
により、布帛とした場合にふくらみ感を付与するという
点から、低収縮であることが好ましい。島成分Bを構成
するポリマの好ましい例としては、実質的にポリエチレ
ンテレフタレート単独重合体でよく、風合を改善するた
めに共重合体、あるいは添加物を加えたものでも良い。
The island component B preferably has a low shrinkage from the viewpoint that it gives a feeling of swelling when a fabric is formed due to the difference in shrinkage ratio with the core component A. As a preferred example of the polymer constituting the island component B, a polyethylene terephthalate homopolymer may be substantially used, or a copolymer or an additive may be added to improve the feel.

【0013】海成分Cとしては、芯成分Aと島成分Bを
容易に分割できることが好ましく、そのためには芯成分
Aおよび島成分Bに対して、アルカリ減量比が30以上
高いポリマであることが好ましく、熱水可溶性ポリエス
テルであることがより好ましい。なお、アルカリ減量比
は以下の方法で測定する。本発明のポリマA、Bおよび
ポリマCからなる同一デニールの円形断面の各フィラメ
ントを3%苛性ソーダ水溶液に浴比1:125、温度9
8〜100℃で処理し、減量率が70%に到達するまで
の所要時間TA 、TB 、TC を測定し、ポリマCのポリ
マAおよびBに対するアルカリ減量比を次式により求め
た。 ポリマCのポリマAに対するアルカリ減量比=TA /T
C ポリマCのポリマBに対するアルカリ減量比=TB /T
C また、減量率はアルカリ処理前の重量をW0 、アルカリ
処理後の重量をW1 として、次式により求めた。 減量率(%)=(W0 −W1 )/W0 ×100
As the sea component C, it is preferable that the core component A and the island component B can be easily separated. For that purpose, a polymer having an alkali weight loss ratio higher than that of the core component A and the island component B by 30 or more is required. It is preferably hot water-soluble polyester. The alkali weight loss ratio is measured by the following method. Each filament having the same denier circular cross-section, which is composed of the polymers A, B and C of the present invention, is added to a 3% aqueous solution of caustic soda at a bath ratio of 1: 125 and a temperature of 9
The treatment was carried out at 8 to 100 ° C., the required time TA, TB and TC until the weight loss rate reached 70% were measured, and the alkali weight loss ratio of the polymer C to the polymers A and B was calculated by the following formula. Alkali weight loss ratio of Polymer C to Polymer A = TA / T
Alkali weight loss ratio of C polymer C to polymer B = TB / T
C The weight loss rate was calculated by the following equation, where W0 is the weight before alkali treatment and W1 is the weight after alkali treatment. Weight loss rate (%) = (W0-W1) / W0 × 100

【0014】また、熱水溶解性は以下の方法で測定す
る。95℃の熱水100gにチップ1gを投入し、マグ
ネチックスターラーで攪拌しながら15分間溶解させ、
実質的にポリマが溶解するものを熱水可溶性とした。
海成分Cとして熱水可溶性ポリエステルを用いることが
より好ましい理由は以下の通りである。
The hot water solubility is measured by the following method. 1 g of chips was added to 100 g of hot water at 95 ° C. and dissolved with a magnetic stirrer for 15 minutes,
A substance in which a polymer was substantially dissolved was made soluble in hot water.
The reason why it is more preferable to use hot water-soluble polyester as the sea component C is as follows.

【0015】第1の理由は、海成分Cの溶解除去後の芯
成分Aと島成分Bとの収縮率差をより大きく発現させる
ことが可能となり、布帛とした際に、より大きなふくら
み感を付与することができることである。すなわち、海
成分Cとして熱水可溶性ポリエステルを用いることによ
って、別に溶解工程を設けることなしに、精練工程にお
いて海成分Cを溶解除去することができるため、芯成分
Aと島成分Bを分離するまでの熱履歴を最小限に抑える
ことができる。このように分離するまでの熱履歴を最小
限に抑えることによって、海成分Cの溶解除去後の芯成
分Aと島成分Bとの収縮率差をより大きく発現させるこ
とが可能となるのである。
The first reason is that the difference in shrinkage between the core component A and the island component B after the sea component C is dissolved and removed can be made larger, and a larger swelling feeling can be obtained when the fabric is formed. It can be given. That is, by using the hot water-soluble polyester as the sea component C, the sea component C can be dissolved and removed in the refining process without providing a separate dissolution process. Therefore, until the core component A and the island component B are separated. The thermal history of can be minimized. By minimizing the thermal history until the separation in this way, it becomes possible to make the shrinkage difference between the core component A and the island component B after the sea component C have been dissolved and removed larger.

【0016】第2の理由は、海成分溶解除去後の繊維強
度を高く維持できることである。すなわち、熱アルカリ
水溶液を用いることなしに海成分の溶解除去ができるた
め、海成分の溶解除去の際に芯成分Aおよび島成分Bの
劣化は全く起こらず、従って海成分溶解除去後の繊維強
度を高く維持できるのである。
The second reason is that the fiber strength after dissolution and removal of sea components can be maintained high. That is, since the sea component can be dissolved and removed without using a hot alkaline aqueous solution, the core component A and the island component B are not deteriorated at all when the sea component is dissolved and removed, and therefore the fiber strength after the sea component is dissolved and removed. Can be kept high.

【0017】第3の理由は、布帛製造工程を簡略化でき
ることである。すなわち、精練工程で海成分を溶解除去
することができるため、熱アルカリ水溶液による海成分
溶解除去工程を省略することができ、安全衛生面および
製造コスト面で著しく改善することができるのである。
The third reason is that the fabric manufacturing process can be simplified. That is, since the sea component can be dissolved and removed in the scouring step, the sea component dissolving and removing step using the hot alkaline aqueous solution can be omitted, and the safety and hygiene and the manufacturing cost can be remarkably improved.

【0018】海成分Cとして用いる熱水可溶性ポリエス
テルは、主たる酸成分がテレフタル酸であり、共重合成
分として5−ナトリウムスルホイソフタル酸およびイソ
フタル酸を総量として20モル%以上50モル%以下共
重合した熱水可溶性ポリエステルであることが特に好ま
しい。5−ナトリウムスルホイソフタル酸およびイソフ
タル酸成分の総共重合量が20モル%未満の場合、十分
な熱水可溶性を得ることができずフレーク状の不溶物が
残存するため好ましくない。逆に、5−ナトリウムスル
ホイソフタル酸およびイソフタル酸成分の総共重合量が
50モル%を越えると、熱水可溶性は十分であるが、冷
水でも一部溶出されるようになり、取扱い上好ましくな
い。
The hot water-soluble polyester used as the sea component C has terephthalic acid as a main acid component, and 5-sodium sulfoisophthalic acid and isophthalic acid as copolymerization components are copolymerized in a total amount of 20 mol% or more and 50 mol% or less. A hot water-soluble polyester is particularly preferable. When the total copolymerization amount of 5-sodium sulfoisophthalic acid and the isophthalic acid component is less than 20 mol%, sufficient hot water solubility cannot be obtained and flaky insoluble matter remains, which is not preferable. On the contrary, when the total copolymerization amount of 5-sodium sulfoisophthalic acid and the isophthalic acid component exceeds 50 mol%, hot water solubility is sufficient, but cold water also partially elutes, which is not preferable in handling. .

【0019】本発明の複合繊維を形成するポリマA、
B、Cには、本発明の効果を阻害しない範囲で艶消剤、
抗酸化剤、蛍光増白剤、難燃剤、紫外線吸収剤などの添
加剤を含有させることもできる。
Polymer A forming the composite fiber of the present invention,
B and C are matting agents within a range that does not impair the effects of the present invention,
Additives such as antioxidants, optical brighteners, flame retardants, and ultraviolet absorbers can also be included.

【0020】本発明による複合繊維を紡糸するのに必要
な紡糸パックは、特開昭57−47938号公報の第3
図や特開昭57−82526号公報の第2図に示される
装置が好適な一例として使用できる。また本発明による
複合繊維を紡糸するのに必要な口金は、図3に示すよう
な特開平1−14321号公報に示される装置が好適な
一例として使用できる。
The spinning pack required for spinning the conjugate fiber according to the present invention is described in JP-A-57-47938, No. 3
The apparatus shown in FIG. 2 and FIG. 2 of JP-A-57-82526 can be used as a suitable example. As the spinneret required for spinning the composite fiber according to the present invention, a device shown in FIG. 3 and disclosed in JP-A-1-14321 can be used as a suitable example.

【0021】本発明による複合繊維を製糸するにあたっ
ては、紡糸および延伸工程を連続して行なう方法、未延
伸糸として一旦巻き取った後、延伸する方法または高速
製糸法等の何れのプロセスにも適用することができる。
また、必要に応じて仮撚や、空気交絡等の糸加工を施し
ても良い。
In producing the conjugate fiber according to the present invention, it can be applied to any process such as a method of continuously performing spinning and drawing steps, a method of once winding as an undrawn yarn and then drawing, or a high-speed yarn making method. can do.
If necessary, false twisting or yarn processing such as air entanglement may be performed.

【0022】[0022]

【実施例】以下、実施例により本発明をより具体的に説
明する。なお、実施例中において用いられる特性等の測
定法は以下の通りである。
The present invention will be described in more detail with reference to the following examples. The methods for measuring the characteristics and the like used in the examples are as follows.

【0023】(a)断面複合状態安定性 カチオン染料、あるいは分散染料で海成分を主に染色し
た後、厚さ5ミクロンにカットし、該染色断面より複合
状態を観察した。 ◎ :複合異常は全くなし ○ :複合異常の単繊維がマルチフィラメント糸の10
%未満 △ :複合異常の単繊維がマルチフィラメント糸の10
%以上30%未満 × :複合異常の単繊維がマルチフィラメント糸の30
%以上
(A) Cross-sectional composite state stability After mainly dyeing the sea component with a cationic dye or a disperse dye, it was cut to a thickness of 5 μm and the composite state was observed from the dyed cross section. ⊚: No composite abnormalities ○: Ten single fibers with composite abnormalities are multifilament yarns
Less than% △: The abnormal composite single fiber is 10 of the multifilament yarn
% Or more and less than 30% x: 30 abnormal composite single fibers are multifilament yarns
%that's all

【0024】(b)高次加工工程通過性 製織時の糸切れ発生頻度から3段階で評価した。 ○:糸切れ全くなし △:糸切れはないが毛羽発生あり ×:糸切れあり(B) Passability in higher-order processing process Evaluation was made on the basis of the frequency of occurrence of yarn breakage during weaving in three stages. ◯: No thread breakage Δ: No thread breakage, but fluff occurred ×: Thread breakage

【0025】(c)風合評価 高級衣料用布帛として重要な基本的風合である「張り
腰」、「ソフトタッチな風合」、「ふくらみ感」の3種
について熟練技術者10名による官能評価を実施し、各
々について従来の混繊糸使いを基準(5点)として10
点満点で評価した。得られた得点を平均し、0点以上2
点未満を××、2点以上4点未満を×、4点以上6点未
満を△、6点以上8点未満を○、8点以上10点以下を
◎として、5段階で評価した。 ◎ :特に優れている ○ :優れている △ :普通 × :劣っている ××:特に劣っている
(C) Evaluation of Feeling Three kinds of basic feelings, which are important feelings as a cloth for high-grade clothes, "tension waist", "soft touch feeling", and "bulging feeling", are sensed by 10 skilled engineers. An evaluation was conducted, and for each of them, the conventional use of mixed yarn was used as a standard (5 points) and 10
It was evaluated on a perfect score. Average the obtained scores, 0 or more 2
A score of less than 4 was rated as 5 ×, a score of 2 or more and less than 4 was rated as ×, a score of 4 or more and less than 6 was rated as Δ, a score of 6 or more and less than 8 was rated as ◯, and a score of 8 or more and 10 or less was rated as ⊚. ◎: Especially excellent ○: Excellent △: Normal ×: Inferior × ×: Especially inferior

【0026】(d)引裂強力 JIS L 1096に準ずる。(D) Tear strength According to JIS L 1096.

【0027】実施例1〜5および比較例1、2 島成分Bとして溶融粘度1450ポイズのポリエチレン
テレフタレートを、芯成分Aとしてイソフタル酸7.1
モル%、2,2ビス{4−(2−ヒドロキシエトキシ)
フェニル}プロパンを4.0モル%共重合した溶融粘度
1520ポイズの変性ポリエステルを、海成分Cとして
5−ソジウムスルホイソフタル酸7.0モル%共重合し
た表1のように溶融粘度の異なる変性ポリエステル用
い、芯成分A、島成分Bおよび海成分Cの複合比A/B
/Cを40/47/13、島成分Bの数を7とし、紡糸温度29
0℃、1500m/分の速度で巻き取った。次いで延伸
を行ない、90デニール、12フィラメントのマルチフ
ィラメント糸を得た(海成分溶解分割後、芯成分は3デ
ニール、島成分は0.5デニールである)。得られた糸
の特性を表2に示す。尚、海成分Cは、いずれも熱水に
対しては不溶であった。該マルチフィラメント糸を用い
て緯糸打込みを行ない平織物を得た。該織物を濃度2%
の苛性ソーダ水溶液中で98〜100℃で30分間減量
処理を行ない、海成分を溶解除去し、弛緩状態で200
℃、5分間の乾熱処理、染色、仕上加工を行なった。表
3に得られた織物の工程通過性、実用特性を示す。
Examples 1-5 and Comparative Examples 1 and 2 Polyethylene terephthalate having a melt viscosity of 1450 poise as the island component B and isophthalic acid 7.1 as the core component A.
Mol%, 2,2 bis {4- (2-hydroxyethoxy)
A modified polyester having a melt viscosity of 1520 poise copolymerized with 4.0 mol% of phenyl} propane was copolymerized with 7.0 mol% of 5-sodium sulfoisophthalic acid as a sea component C. Using polyester, composite ratio A / B of core component A, island component B, and sea component C
/ C is 40/47/13, the number of island components B is 7, and the spinning temperature is 29.
It was wound at 0 ° C. and a speed of 1500 m / min. Next, drawing was carried out to obtain a multifilament yarn of 90 denier and 12 filaments (after the sea component was dissolved and divided, the core component was 3 denier and the island component was 0.5 denier). The characteristics of the obtained yarn are shown in Table 2. The sea component C was insoluble in hot water. Using the multifilament yarn, weft driving was performed to obtain a plain woven fabric. Concentration of the fabric is 2%
In a caustic soda aqueous solution, the weight reduction treatment is performed at 98 to 100 ° C for 30 minutes to dissolve and remove sea constituents, and to remove 200% in a relaxed state.
Dry heat treatment at 5 ° C for 5 minutes, dyeing, and finishing were performed. Table 3 shows the process passability and practical properties of the obtained woven fabric.

【0028】比較例1では、海成分Cに対する芯成分A
および島成分Bの溶融粘度の比が大きすぎるため、原糸
強度および海成分溶解除去後の繊維強度は高いが複合形
態の安定性に欠け、複合異常による製糸性が悪化し、ま
た品位の点でも複合異常により安定した品位の製品を得
ることが困難であった。また、比較例2では、海成分C
に対する芯成分Aおよび島成分Bの溶融粘度の比が小さ
すぎるため、複合形態の安定性は良好であるが原糸強度
が低く、製織時の糸切れ等のトラブルが発生し高次加工
工程の通過性が悪化すると共に、海成分溶解除去後の繊
維強度低下が大きく、布帛の引裂強力が低下し、実用に
十分耐え得る製品を得ることが困難であった。
In Comparative Example 1, the core component A with respect to the sea component C
Since the ratio of the melt viscosity of the island component B and the island component B is too large, the strength of the raw yarn and the fiber strength after the dissolution and removal of the sea component are high, but the stability of the composite form is lacking, and the yarn formability is deteriorated due to the composite abnormality. However, it was difficult to obtain a stable quality product due to complex abnormalities. In Comparative Example 2, the sea component C
Since the ratio of the melt viscosities of the core component A and the island component B to the core component is too small, the stability of the composite form is good, but the raw yarn strength is low, and problems such as yarn breakage during weaving occur and high-order processing It is difficult to obtain a product that can withstand practical use because the passage property is deteriorated, the fiber strength is greatly reduced after the sea component is dissolved and removed, and the tear strength of the fabric is decreased.

【0029】実施例1および2では、海成分Cに対する
芯成分Aおよび島成分Bの溶融粘度の比がやや大きく、
複合形態の安定性が若干劣っていたが、原糸強度および
海成分溶解除去後の繊維強度は高く、高次加工通過性お
よび布帛の引裂強力は非常に良好であり、風合面でも適
度な張り・腰、芯成分Aと島成分Bとの収縮率差による
ふくらみ感、島成分Bの偏平化によるドライ感のあるピ
ーチタッチな風合を有しており、従来にない優れた特徴
を有していた。また、実施例5では、複合形態の安定性
が非常に良好であり、風合面でも適度な張り・腰、ふく
らみ感および島成分Bの偏平化によるドライ感のあるピ
ーチタッチな風合を有しており、従来にない優れた特徴
を有していたが、海成分溶解除去後の繊維強度が若干低
いため、引裂強力が若干低いものであった。また、実施
例3および4では、原糸強度、海成分溶解除去後の繊維
強度、複合形態の安定性、高次加工通過性とも非常に良
好であり、得られた布帛の風合も適度な張り・腰、ふく
らみ感およびドライ感のあるピーチタッチな風合を有し
ており、従来にない優れた特徴を有していた。
In Examples 1 and 2, the ratio of the melt viscosity of the core component A and the island component B to the sea component C was rather large,
The stability of the composite form was slightly inferior, but the strength of the raw yarn and the fiber strength after dissolution and removal of the sea component were high, the high-order processability and the tear strength of the fabric were very good, and the texture was also appropriate. Tension / waist, swelling due to difference in shrinkage ratio between core component A and island component B, and dry feeling due to flattening of island component B have a peach-touch feel, and have outstanding features that have never existed before. Was. In addition, in Example 5, the stability of the composite form is very good, and even on the texture side, there is a feeling of moderate tension / waist, swelling, and dry feeling due to the flatness of the island component B, and a peach-touch feeling. Although it had excellent characteristics that were not available in the past, the fiber strength after dissolution and removal of sea components was slightly low, and therefore the tear strength was slightly low. In addition, in Examples 3 and 4, the raw yarn strength, the fiber strength after dissolution and removal of the sea component, the stability of the composite form, and the high-order processing passability are very good, and the texture of the obtained fabric is also appropriate. It had a peach-touch texture with firmness / waist, swelling and dryness, and had outstanding features that were unprecedented.

【0030】比較例3 芯成分A、島成分Bおよび海成分Cの溶融粘度をそれぞ
れ表1のように変更して実施例1と同様の方法で紡糸、
延伸を行ないマルチフィラメント糸を得た(海成分溶解
分割後、芯成分は3デニール、島成分は0.5デニール
である)。得られた糸の特性を表2に示す。実施例1と
同様に平織物を作製し、仕上加工を行なった。表3に得
られた織物の工程通過性、実用特性を示す。
Comparative Example 3 Spinning was carried out in the same manner as in Example 1, except that the melt viscosities of the core component A, the island component B and the sea component C were changed as shown in Table 1.
Stretching was performed to obtain a multifilament yarn (after the sea component was dissolved and divided, the core component was 3 denier and the island component was 0.5 denier). The characteristics of the obtained yarn are shown in Table 2. A plain woven fabric was prepared in the same manner as in Example 1 and subjected to finishing processing. Table 3 shows the process passability and practical properties of the obtained woven fabric.

【0031】比較例3は、海成分Cに対する芯成分Aお
よび島成分Bの溶融粘度比は十分満足し、原糸強度とし
ては高いが、海成分溶解除去後の繊維強度の低下が大き
いため、高次加工工程通過性が不良であるとともに引裂
強力が低く、実用に十分耐え得る製品を得ることが困難
であった。
In Comparative Example 3, the melt viscosity ratio of the core component A and the island component B to the sea component C was sufficiently satisfied, and although the raw yarn strength was high, the fiber strength after the sea component was dissolved and removed was large, so that It was difficult to obtain a product that could withstand practical use because it had poor passability in high-order processing steps and low tear strength.

【0032】[0032]

【表1】 [Table 1]

【表2】 [Table 2]

【表3】 実施例6〜9 実施例4で使用したポリマを用いて、島成分Bの島数を
表4のように変更して実施例4と同様の方法で紡糸、延
伸を行ないマルチフィラメント糸を得た(海成分溶解分
割後、芯成分は3デニール、島成分は0.5デニールで
ある)。得られた糸の特性を表4に示す。実施例4と同
様に平織物を作製し、仕上加工を行なった。表5に得ら
れた織物の工程通過性、実用特性を示す。
[Table 3] Examples 6 to 9 Using the polymer used in Example 4, the number of islands of the island component B was changed as shown in Table 4, and spinning and drawing were performed in the same manner as in Example 4 to obtain multifilament yarns. (After sea component dissolution and splitting, the core component is 3 denier and the island component is 0.5 denier). The characteristics of the obtained yarn are shown in Table 4. A plain weave fabric was prepared and finished as in Example 4. Table 5 shows the process passability and practical properties of the obtained woven fabric.

【0033】実施例6では、原糸強度、海成分溶解除去
後の繊維強度、複合形態の安定性、高次加工通過性等に
非常に優れていたが、風合面において、島成分Bの偏平
度が非常に大きいため、島成分の偏平面に対する曲げ剛
性の低下によりふくらみ感が若干不足し、また島数が少
ないことによりピーチタッチ感も若干低下していた。ま
た実施例9では、複合形態の安定性、高次加工通過性等
に非常に優れていたが、海成分溶解除去後の繊維強度が
若干低いため、引裂強力が若干低かった。また風合面に
おいても、ピーチタッチな風合は得られるが島成分Bの
偏平度が小さいため、偏平化によるドライ感は不足して
いた。実施例7および8では、原糸強度、海成分溶解除
去後の繊維強度、複合形態の安定性および工程通過性が
非常に良好であり、風合面においても、適度な張り・
腰、芯成分と島成分の収縮差によるふくらみ感、島成分
Bの偏平化によるドライ感のあるピーチタッチな風合を
有しており、従来にない優れた特徴を有していた。
In Example 6, the strength of the raw yarn, the strength of the fiber after dissolution and removal of the sea component, the stability of the composite morphology, the high-order processing passability, etc. were very excellent. Since the flatness was very large, the bending stiffness of the island component with respect to the flat plane was slightly reduced, and the swelling feeling was slightly insufficient, and the peach touch feeling was also slightly reduced due to the small number of islands. Further, in Example 9, the stability of the composite form, the high-order processing passability, etc. were very excellent, but the tear strength was slightly low because the fiber strength after dissolution and removal of the sea component was slightly low. Also on the texture surface, a peach-touch texture was obtained, but the flatness of the island component B was small, so the dry feeling due to flattening was insufficient. In Examples 7 and 8, the strength of the raw yarn, the strength of the fiber after dissolution and removal of the sea component, the stability of the composite form, and the process passability are very good, and even in the texture surface, a suitable tension
It had a swelling feeling due to the difference in contraction between the waist and core components and the island component, and a peach-touch texture with a dry feeling due to the flattening of the island component B, and had excellent features that were not previously available.

【0034】[0034]

【表4】 [Table 4]

【表5】 実施例10〜13および比較例4、5 実施例7において海成分Cとして5−ナトリウムスルホ
イソフタル酸10.0モル%、およびイソフタル酸35
モル%を共重合した表6のように溶融粘度の異なる熱水
可溶性ポリエステル用い、島数を5として実施例7と同
様の方法で紡糸、延伸を行ないマルチフィラメント糸を
得た(海成分溶解分割後、芯成分は3デニール、島成分
は0.4デニールである)。得られた糸の特性を表7に
示す。なお、海成分Cの芯成分Aおよび島成分Bに対す
るアルカリ減量比は、海成分Cが数秒で完全溶解してし
まうため、詳細な減量比が測定不能のため500以上と
判断した。また、海成分Cの熱水溶解性については、い
ずれも良好な溶解性を有していた。実施例1と同様に平
織物を作製し、該織物を98℃のトリポリリン酸ソーダ
0.2g/l熱水溶液中で10分間減量処理を行ない海
成分Cを溶解除去し、弛緩状態で200℃、5分間の乾
熱処理、染色、仕上加工を行なった。表8に得られた織
物の工程通過性、実用特性を示す。
[Table 5] Examples 10 to 13 and Comparative Examples 4 and 5 In Example 7, as the sea component C, 10.0 mol% of 5-sodium sulfoisophthalic acid and 35 of isophthalic acid.
Using hot water-soluble polyesters having different melt viscosities as shown in Table 6 in which mol% was copolymerized, the number of islands was set to 5, and spinning and drawing were performed in the same manner as in Example 7 to obtain a multifilament yarn (sea component dissolution division). Later, the core component is 3 denier and the island component is 0.4 denier). The characteristics of the obtained yarn are shown in Table 7. The alkali weight loss ratio of the sea component C to the core component A and the island component B was determined to be 500 or more because the sea component C was completely dissolved in a few seconds and the detailed weight loss ratio could not be measured. Regarding the hot water solubility of the sea component C, all had good solubility. A plain woven fabric was prepared in the same manner as in Example 1, and the woven fabric was subjected to weight reduction treatment in a hot aqueous solution of sodium tripolyphosphate (0.2 g / l) at 98 ° C. for 10 minutes to dissolve and remove the sea component C. Dry heat treatment for 5 minutes, dyeing, and finishing were performed. Table 8 shows the process passability and practical properties of the obtained woven fabric.

【0035】比較例4では、海成分Cに対する芯成分A
および島成分Bの溶融粘度の比が大きすぎるため、複合
形態の安定性に欠け、複合異常による製糸性が悪化し、
また品位の点でも複合異常により安定した品位の製品を
得ることが困難であった。また、比較例5では、海成分
Cに対する芯成分Aおよび島成分Bの溶融粘度の比が小
さすぎるため原糸強度が低く、製織時の糸切れ等のトラ
ブルが発生し高次加工工程の通過性が悪化すると共に、
海成分溶解除去後の繊維強度が低いため、布帛の引裂強
力が低下し、実用に十分耐え得る製品を得ることが困難
であった。
In Comparative Example 4, the core component A with respect to the sea component C
And the melt viscosity ratio of the island component B is too large, the stability of the composite form is lacking, and the yarn formability is deteriorated due to the composite abnormality.
Also, in terms of quality, it was difficult to obtain a stable quality product due to a complex abnormality. Further, in Comparative Example 5, since the ratio of the melt viscosity of the core component A and the island component B to the sea component C is too small, the strength of the raw yarn is low, and troubles such as yarn breakage during weaving occur and passing through a high-order finishing process. As the sex worsens,
Since the fiber strength after dissolving and removing the sea component is low, the tear strength of the fabric is lowered, and it is difficult to obtain a product that can withstand practical use.

【0036】実施例10および11では、海成分Cに対
する芯成分Aおよび島成分Bの溶融粘度の比がやや大き
く、複合形態の安定性が若干劣っていたが、原糸強度お
よび海成分溶解除去後の繊維強度は高く、高次加工通過
性および布帛の引裂強力は非常に良好であり、風合面で
も適度な張り・腰、芯成分Aと島成分Bとの収縮率差に
よるふくらみ感、島成分Bの偏平化によるドライ感のあ
るピーチタッチな風合を有しており、従来にない優れた
特徴を有していた。
In Examples 10 and 11, the melt viscosity ratios of the core component A and the island component B to the sea component C were rather large, and the stability of the composite morphology was slightly inferior. The subsequent fiber strength is high, high-order processability and tear strength of the fabric are very good, moderate tension and waist on the textured surface, and swelling due to the difference in shrinkage ratio between the core component A and the island component B, It had a dry and peach-touch texture due to the flattening of the island component B, and had excellent features that were not available in the past.

【0037】実施例12および13では、原糸強度、海
成分溶解除去後の繊維強度、複合形態の安定性、高次加
工通過性とも非常に良好であり、得られた布帛の風合も
適度な張り・腰、芯成分と島成分の収縮差によるふくら
み感および島成分Bの偏平化によるドライ感のあるピー
チタッチな風合を有しており、従来にない優れた特徴を
有していた。
In Examples 12 and 13, the raw yarn strength, the fiber strength after dissolution and removal of the sea component, the stability of the composite form, and the high-order processing passability were very good, and the texture of the obtained fabrics was also appropriate. It has a peach-touch feel with a firmness and waist, a swelling feeling due to the difference in contraction between the core component and the island component, and a dry feeling due to the flattening of the island component B, and had excellent features that have never been seen before. .

【0038】[0038]

【表6】 [Table 6]

【表7】 [Table 7]

【表8】 実施例14〜16 実施例12において海成分Cとして5−ナトリウムスル
ホイソフタル酸およびイソフタル酸の共重合量を表9の
ように変更した熱水可溶性ポリエステル用い、島数を1
0として、実施例12と同様の方法で紡糸、延伸を行な
いマルチフィラメント糸を得た(海成分溶解分割後、芯
成分は4デニール、島成分は0.5デニールである)。
得られた糸の特性を表10に示す。海成分Cの熱水溶解
性については、実施例14で用いたものは熱水では完全
に溶解することができず不溶物が残存した。また、実施
例16で用いたものは冷水に対しても一部が溶解した。
一方、実施例15で用いたものは良好な溶解性を有して
いた。また、海成分Cの芯成分Aおよび島成分Bに対す
るアルカリ減量比は、海成分Cが数秒で完全溶解してし
まうため、詳細な減量比が測定不能のため500以上と
判断した。実施例12と同様に平織物を作製し、仕上加
工を行なった。表11に得られた織物の工程通過性、実
用特性を示す。
[Table 8] Examples 14 to 16 In Example 12, hot water-soluble polyester having a copolymerization amount of 5-sodium sulfoisophthalic acid and isophthalic acid changed as shown in Table 9 as sea component C was used, and the number of islands was 1
A multifilament yarn was obtained by carrying out spinning and drawing in the same manner as in Example 12 as 0 (after the sea component was melted and divided, the core component was 4 denier and the island component was 0.5 denier).
The characteristics of the obtained yarn are shown in Table 10. Regarding the solubility of sea component C in hot water, the one used in Example 14 could not be completely dissolved in hot water and an insoluble matter remained. Further, the material used in Example 16 was partially dissolved in cold water.
On the other hand, the one used in Example 15 had good solubility. The alkali weight loss ratio of the sea component C to the core component A and the island component B was determined to be 500 or more because the detailed weight loss ratio could not be measured because the sea component C was completely dissolved in a few seconds. A plain weave fabric was prepared in the same manner as in Example 12, and finishing processing was performed. Table 11 shows the process passability and practical properties of the obtained woven fabric.

【0039】実施例14では、原糸強度、海成分溶解除
去後の繊維強度、複合形態の安定性、高次加工通過性と
も非常に良好であり、得られた布帛の風合も適度な張り
・腰、ふくらみ感および島成分Bの偏平化によるドライ
感のあるピーチタッチな風合を有しており、従来にない
優れた特徴を有していたが、海成分Cの熱水溶解性が十
分でないために若干の不溶物が残存しており、品位の面
で若干劣っていた。
In Example 14, the strength of the raw yarn, the strength of the fiber after dissolution and removal of the sea component, the stability of the composite form, and the ability to pass through high-order processing are very good, and the obtained fabric has a suitable feel.・ It has a peach-touch feel with a waist, swelling feeling and a flat feeling of the island component B with a dry feeling, and it had excellent characteristics not previously available, but the hot water solubility of the sea component C was Since it was not sufficient, some insoluble matter remained, and the quality was slightly inferior.

【0040】実施例16では、原糸強度、海成分溶解除
去後の繊維強度、複合形態の安定性とも非常に良好であ
り、得られた布帛の風合も適度な張り・腰、芯成分と島
成分の収縮差によるふくらみ感および島成分Bの偏平化
によるドライ感のあるピーチタッチな風合を有してお
り、従来にない優れた特徴を有していたが、海成分Cが
冷水においても一部溶解してしまうため、製織時に若干
の毛羽発生が起こり、高次加工通過性の面で若干劣って
いた。
In Example 16, the strength of the raw yarn, the strength of the fiber after dissolution and removal of the sea component, and the stability of the composite form were very good, and the obtained fabric had a suitable feel, waist and core component. It had a peachy touch with a swelling feeling due to the difference in shrinkage of the island component and a dry feeling due to the flattening of the island component B, and had excellent features that were not available in the past, but the sea component C was used in cold water. Since some of them also melted, some fluff was generated during weaving, and it was slightly inferior in terms of high-order processing passability.

【0041】実施例15では、原糸強度、海成分溶解除
去後の繊維強度、複合形態の安定性、高次加工通過性と
も非常に良好であり、得られた布帛の風合も適度な張り
・腰、芯成分と島成分の収縮差によるふくらみ感および
島成分Bの偏平化によるドライ感のあるピーチタッチな
風合を有しており、従来にない優れた特徴を有してい
た。
In Example 15, the strength of the raw yarn, the fiber strength after dissolving and removing the sea component, the stability of the composite form, and the ability to pass through the high-order processing are very good, and the obtained fabric has an appropriate texture. It has a peachy touch with a swelling feeling due to the difference in shrinkage between the waist and core components and the island component, and a dry feeling due to the flattening of the island component B, and had excellent features that were not previously available.

【0042】[0042]

【表9】 [Table 9]

【表10】 [Table 10]

【表11】 [Table 11]

【0043】[0043]

【発明の効果】本発明によるポリエステル系3成分複合
繊維は、海成分Cに対する芯成分Aおよび島成分Bの溶
融粘度の比、および原糸強度と海成分溶解除去後の繊維
強度の比を特定化することにより、複合形態の安定性を
著しく改善することができ、更に工程通過性、実用特性
に優れ、且つ張り・腰、ソフトタッチな風合、およびふ
くらみ感をかね備えた従来にない優れた風合を有する布
帛を安定に製造することができる。
EFFECT OF THE INVENTION The polyester-based three-component conjugate fiber according to the present invention specifies the ratio of the melt viscosity of the core component A and the island component B to the sea component C, and the ratio of the raw yarn strength and the fiber strength after the sea component is dissolved and removed. In addition, the stability of the composite form can be significantly improved, and the process passability and practical properties are also excellent, and it has an unprecedented advantage that has tension / waist, soft touch feeling, and swelling feeling. It is possible to stably manufacture a fabric having a good texture.

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

【図1】本発明の3成分複合繊維を構成する複合繊維の
好ましい一例を示す複合断面図
FIG. 1 is a composite cross-sectional view showing a preferred example of a composite fiber constituting a three-component composite fiber of the present invention.

【図2】図1の複合繊維から海成分を除去して得た糸の
断面図
FIG. 2 is a cross-sectional view of a yarn obtained by removing sea components from the composite fiber of FIG.

【図3】本発明の3成分複合繊維を得るために好ましく
用いられる口金装置の縦断面図
FIG. 3 is a longitudinal sectional view of a spinneret device preferably used to obtain the three-component conjugate fiber of the present invention.

【符号の説明】[Explanation of symbols]

1:芯成分Aの流入孔 2:島成分Bの流入孔 3:海成分Cの流入孔 4:ポリマ集合部 5:口金吐出孔 1: Inflow hole for core component A 2: Inflow hole for island component B 3: Inflow hole for sea component C 4: Polymer gathering part 5: Mouth discharge hole

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 芯成分A、島成分B、海成分Cのいずれ
も相異なる3種のポリエステルからなり、島成分Bが芯
成分Aを取り囲むように点在し、且つ海成分Cのなかに
偏在することなく分散してなる3成分複合繊維におい
て、海成分Cの溶融粘度(εc)に対する芯成分Aおよ
び島成分Bの溶融粘度(εaおよびεb)の比、εa/
εcおよびεb/εcが、いずれも0.80以上、2.
50以下であり、原糸強度(T1)に対する海成分溶解
除去後の繊維強度(T2)の比、T2/T1が1.02
以上であることを特徴とするポリエステル系3成分複合
繊維。
1. The core component A, the island component B, and the sea component C are each composed of three different polyesters, and the island components B are scattered so as to surround the core component A, and in the sea component C. In a three-component composite fiber dispersed without being unevenly distributed, the ratio of the melt viscosity (εa and εb) of the core component A and the island component B to the melt viscosity (εc) of the sea component C, εa /
εc and εb / εc are both 0.80 or more, 2.
It is 50 or less, and T2 / T1 is 1.02, which is the ratio of the fiber strength (T2) after the sea component is dissolved and removed to the raw thread strength (T1).
The above is a polyester-based three-component composite fiber characterized by the above.
【請求項2】 海成分Cとして、熱水可溶性ポリエステ
ルを用いることを特徴とする請求項1に記載したポリエ
ステル系3成分複合繊維。
2. The polyester-based three-component conjugate fiber according to claim 1, wherein hot water-soluble polyester is used as the sea component C.
【請求項3】 海成分Cとして、主たる酸成分がテレフ
タル酸であり、共重合成分として5−ナトリウムスルホ
イソフタル酸およびイソフタル酸を総量として20モル
%以上50モル%以下共重合した熱水可溶性ポリエステ
ルを用いることを特徴とする請求項1および2に記載し
たポリエステル系3成分複合繊維。
3. A hot water-soluble polyester obtained by copolymerizing, as the sea component C, a main acid component of terephthalic acid, and copolymerizing 5-sodium sulfoisophthalic acid and isophthalic acid as a copolymerizing component in a total amount of 20 mol% or more and 50 mol% or less. The polyester-based three-component conjugate fiber according to claim 1 or 2, wherein
JP6102906A 1993-06-16 1994-05-17 Polyester 3-component composite fiber Pending JPH0770827A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6102906A JPH0770827A (en) 1993-06-16 1994-05-17 Polyester 3-component composite fiber

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP5-144638 1993-06-16
JP14463893 1993-06-16
JP6102906A JPH0770827A (en) 1993-06-16 1994-05-17 Polyester 3-component composite fiber

Publications (1)

Publication Number Publication Date
JPH0770827A true JPH0770827A (en) 1995-03-14

Family

ID=26443596

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6102906A Pending JPH0770827A (en) 1993-06-16 1994-05-17 Polyester 3-component composite fiber

Country Status (1)

Country Link
JP (1) JPH0770827A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100231324B1 (en) * 1995-12-29 1999-11-15 구광시 Third component composite fiber
JP2012057291A (en) * 2006-01-31 2012-03-22 Eastman Chem Co Manufacturing method of multicomponent fiber and microdenier fiber derived from sulfopolyester
WO2022107671A1 (en) * 2020-11-20 2022-05-27 東レ株式会社 Sea-island composite polyester fiber

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100231324B1 (en) * 1995-12-29 1999-11-15 구광시 Third component composite fiber
JP2012057291A (en) * 2006-01-31 2012-03-22 Eastman Chem Co Manufacturing method of multicomponent fiber and microdenier fiber derived from sulfopolyester
JP2013136868A (en) * 2006-01-31 2013-07-11 Eastman Chemical Co Multicomponent fiber derived from sulfopolyester and method for producing microdenier fiber
WO2022107671A1 (en) * 2020-11-20 2022-05-27 東レ株式会社 Sea-island composite polyester fiber

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