JPH06240516A - Water absorbing composite fiber - Google Patents

Water absorbing composite fiber

Info

Publication number
JPH06240516A
JPH06240516A JP2909393A JP2909393A JPH06240516A JP H06240516 A JPH06240516 A JP H06240516A JP 2909393 A JP2909393 A JP 2909393A JP 2909393 A JP2909393 A JP 2909393A JP H06240516 A JPH06240516 A JP H06240516A
Authority
JP
Japan
Prior art keywords
fiber
polyester
polyamide
fibers
yarn
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2909393A
Other languages
Japanese (ja)
Inventor
Ryoji Nakamura
良司 中村
Masaki Yamanaka
昌樹 山中
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.)
Toyobo Co Ltd
Original Assignee
Toyobo Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyobo Co Ltd filed Critical Toyobo Co Ltd
Priority to JP2909393A priority Critical patent/JPH06240516A/en
Publication of JPH06240516A publication Critical patent/JPH06240516A/en
Pending legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/28Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
    • D01D5/30Conjugate filaments; Spinnerette packs therefor
    • D01D5/36Matrix structure; Spinnerette packs therefor

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Textile Engineering (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Multicomponent Fibers (AREA)

Abstract

PURPOSE:To provide a composite fiber excellent in water absorption and moisture absorption and most suitable for the field of comfortable clothing. CONSTITUTION:There is provided a composite fiber having a sea-island structure containing inside island components of the cross section of the fiber each composed of a group of polyamide filaments and island components each composed of polyester filaments, having >=1.5 flatness of the cross section and arranged around the polyamide filament groups. This fiber is designed so as to have a specified relation between the number and the single fiber denier of the outside polyester fibers and the inside polyamide fibers and, therefore, characteristically excellent in moisture absorption and water absorption, free from wetness and excellent in comfortability.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は吸汗性、吸湿性にすぐれ
た、快適性衣料分野に最適な合成繊維に関する物であ
り、さらには多発汗時にも快適な衣料用複合糸に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a synthetic fiber which is excellent in sweat absorption and hygroscopicity and is most suitable for the field of comfortable clothes, and further relates to a composite yarn for clothes which is comfortable even when sweating a lot.

【0002】[0002]

【従来の技術】合成繊維は優れた機械的特性や均一性、
イージィーケアー性等より衣料用繊維として大きく発展
してきた。しかしながら均一がうえの問題としてのプラ
スチック感や、触感としての冷たさ等の問題があり、種
々の改良がなされてきており今日の姿に到っている。中
でもポリエステルは異収縮混繊等の糸長差付与技術とア
ルカリ減量技術及び同技術と微細孔形成剤の添加技術の
複合による繊維表面の粗表面化技術により、非常に風合
いの優れた衣料用繊維素材に成長した。
2. Description of the Related Art Synthetic fibers have excellent mechanical properties and uniformity,
It has been greatly developed as a fiber for clothing due to its easy care properties. However, there are problems such as a plastic feeling as a problem of uniformity and a cold feeling as a tactile sensation, and various improvements have been made to reach the present state. Among them, polyester is a fiber material for clothing that has a very excellent texture due to the technique of imparting a yarn length difference such as different shrinkage mixed fibers, the technique of alkali reduction, and the technique of roughening the fiber surface by combining this technique and the technique of adding a micropore-forming agent. Has grown to

【0003】しかしながら、いまだ解決されていない大
きな問題として吸汗性の問題がある。この問題を解決す
る試みとして断面形状や表面形態を考慮して毛管現象を
利用した改善が提案されているが効果は少なく吸汗性合
成繊維の出現には到っていない。また他の改善手段とし
て化学的にポリエステルを改質する方法も提案されてい
る。たとえば元々吸湿性のあるポリアルキレングリコー
ル等を共重合したりブレンドする方法が知られているが
機械的特性の低下が否めないばかりか染色物の耐光性に
著しい低下があり、衣料用途としては使用できる範囲に
かなりの限定を受ける。他の改善策として後加工で親水
性を付与する技術もあるが、特にポリエステルの場合は
耐久性にすぐれた加工剤がない。耐久性をあげる手段と
してアクリル酸等をグラフト重合する方法もあるがポリ
エステルでは膨潤剤が必要であり溶剤の回収の問題や機
械的特性の低下、耐光性の低下等の問題がある。他方、
ポリアミドは水系でグラフト重合ができ問題は少ないも
のの耐光性の低下は免れない。
However, a major problem that has not yet been solved is the problem of sweat absorption. As an attempt to solve this problem, an improvement utilizing the capillary phenomenon in consideration of the cross-sectional shape and surface morphology has been proposed, but the effect is small and the sweat-absorbing synthetic fiber has not yet appeared. As another improvement means, a method of chemically modifying polyester has been proposed. For example, a method of copolymerizing or blending a polyalkylene glycol, which originally has a hygroscopic property, is known, but not only the mechanical properties cannot be declined but also the light resistance of the dyed product is remarkably reduced. The range that can be done is considerably limited. As another improvement measure, there is a technique of imparting hydrophilicity by post-processing, but particularly in the case of polyester, there is no processing agent having excellent durability. There is also a method of graft-polymerizing acrylic acid or the like as a means for increasing durability, but polyester requires a swelling agent, which causes problems such as recovery of solvent, deterioration of mechanical properties, and deterioration of light resistance. On the other hand,
Polyamide can be graft-polymerized in an aqueous system, and although there are few problems, deterioration of light resistance is inevitable.

【0004】また種々の改善による吸湿性の改善効果は
多かれ少なかれ認められるものの、このままでは快適性
にはつながらず、吸湿した水分の肌近傍からの隔離を考
える必要がある特に発汗量が多い場合は、繊維表面に吸
着した水分により衣服が肌にまとわりつき不快に感ずる
ことが多く、繊維の吸水、吸湿能だけでは発汗にたいす
る快適性は議論出来ない。この考えかたを取り入れて糸
表面近傍に疏水性の繊維を配し、中間層に吸湿性の繊維
を、最内部にファインデニール繊維を配し、吸汗水分の
移動性を考慮した3層構造糸も提案されているが複合紡
績糸であることにより審美性に欠け、細い糸にしにくい
と言う欠点もある。
[0004] Although various improvements in hygroscopicity are more or less recognized, it does not lead to comfort as it is, and it is necessary to consider the separation of the absorbed moisture from the vicinity of the skin, especially when the amount of sweat is large. In many cases, clothes adhering to the skin feel uncomfortable due to the moisture adsorbed on the fiber surface, and the comfort of sweating cannot be discussed only by the water absorption and moisture absorption capabilities of the fiber. Taking this concept into consideration, hydrophobic fibers are arranged in the vicinity of the yarn surface, hygroscopic fibers are arranged in the middle layer, and fine denier fibers are arranged in the innermost part. However, there is a drawback in that the spun yarn is poor in aesthetics and it is difficult to make a thin yarn because it is a composite spun yarn.

【0005】[0005]

【発明が解決しようとする課題】本発明は、前記従来の
欠点を解消し、ベトつき感がない上に吸水性、吸湿性に
優れ、且つ、フィラメント糸特有の優美さを兼ね備えた
布帛に適した複合繊維を提供せんとするものである。
DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned drawbacks of the prior art and is suitable for a fabric having no sticky feeling, excellent water absorbency and hygroscopicity, and an elegance peculiar to filament yarn. It is intended to provide composite fibers.

【0006】[0006]

【課題を解決するための手段】上記課題を解決するため
の手段、即ち本発明は、内側島成分として配されたポリ
アミド繊維群と該ポリアミド繊維群を取り囲むように最
外周島成分として配されたポリエステル繊維群と、溶剤
に対して溶解性の大きいポリマーよりなる海成分からな
る複合繊維であり、該複合繊維中のポリアミド繊維は複
合繊維に対して50重量%以上の割合で存在し、最外周
島成分として配されたポリエステル繊維の断面は偏平度
が1.5以上であり、かつ、最外周に配されたポリエス
テル繊維の単糸デニール(do)および繊維本数(N
o)と内側に配されたポリアミド繊維の単糸デニール
(di)および繊維本数(Ni)が下記(1)式および
(2)式を満足することを特徴とする複合繊維である。 3.0≧do>di≧0.2 ・・・・・・・・・・ (1) 6≦No<Ni≦30 ・・・・・・・・・・ (2) (但し、上記偏平度は、長軸長さ/短軸長さをもって表
わす。)
Means for Solving the Problems The means for solving the above-mentioned problems, that is, the present invention, is a polyamide fiber group arranged as an inner island component and an outermost island component so as to surround the polyamide fiber group. A composite fiber comprising a polyester fiber group and a sea component composed of a polymer having high solubility in a solvent, wherein the polyamide fiber in the composite fiber is present in a proportion of 50% by weight or more based on the composite fiber, The polyester fiber arranged as an island component has a flatness of 1.5 or more, and the polyester fiber arranged at the outermost periphery has a single yarn denier (do) and the number of fibers (N
o) and the single yarn denier (di) and the number of fibers (Ni) of the polyamide fibers arranged inside satisfy the following formulas (1) and (2). 3.0 ≧ do> di ≧ 0.2 (1) 6 ≦ No <Ni ≦ 30 (2) (However, the above flatness Is expressed as major axis length / minor axis length.)

【0007】本発明の重要なポイントは複合繊維の構造
にあり、原糸断面の外周を疎水性とし原糸断面の内部を
親水性とすることが重要である。このことにより発汗時
の水滴を原糸内部に取り込み原糸の表層は乾いた状態に
保つことができる。この目的を溶融紡糸可能な合成繊維
用ポリマーで達成するためには、原糸の外層を構成する
繊維を疎水性のポリエステルとし原糸の内部を構成する
繊維の多くを親水性のポリアミドとする必要がある。原
糸の内部を構成する繊維はポリエステルとポリアミドの
混繊状態でも良いがこの時のポリアミドの構成比は50
%以上にする必要がある。50%未満では親水性繊維を
内部に入れ保水性能を高めた効果が発揮されない。また
疎水性のポリエステルと親水性のポリアミドの組合せと
することにより、水系の処理剤をもちいアクリル酸等を
親水性のポリアミドのみに選択的にグラフト重合するこ
とができ原糸内部だけを吸湿性を高めることも出来る。
両者の組合せで2層構造糸を作る方法として、両者を別
々に製糸し、後で混繊して2層構造糸とすることも不可
能ではないが、構造の完成度(2層構造の繊維配置適性
確立)が良くないことや製布工程で受ける種々の屈曲や
扱きにより2層構造の破壊を考えると理想的ではない。
The important point of the present invention lies in the structure of the composite fiber, and it is important that the outer periphery of the raw yarn cross section is hydrophobic and the inside of the raw yarn cross section is hydrophilic. As a result, water drops during sweating can be taken into the inside of the yarn and the surface layer of the yarn can be kept dry. In order to achieve this object with a melt-spinnable polymer for synthetic fibers, it is necessary to make the fibers forming the outer layer of the raw yarn hydrophobic polyester and most of the fibers constituting the inside of the raw yarn hydrophilic polyamide. There is. The fibers composing the inside of the raw yarn may be a mixed state of polyester and polyamide, but the composition ratio of polyamide at this time is 50
Must be at least%. If it is less than 50%, the effect of putting hydrophilic fibers inside and improving the water retention performance cannot be exhibited. In addition, by using a combination of hydrophobic polyester and hydrophilic polyamide, it is possible to selectively polymerize acrylic acid and the like with hydrophilic polyamide only by using a water-based treating agent, and to increase hygroscopicity only inside the yarn. It can be increased.
As a method of producing a two-layer structure yarn by combining the two, it is not impossible to separately produce the both and then mix them to form a two-layer structure yarn, but the degree of perfection of the structure (two-layer structure fiber This is not ideal considering the fact that the establishment of the placement suitability) is not good and that the two-layer structure is broken due to various bends and handles received in the fabric making process.

【0008】本発明糸は紡糸工程で完全な2層構造を形
成し、溶出成分で形態を固定したまま、製糸、製布、精
練、熱セットを経た後、溶出成分を溶出するため布構造
の拘束力や、熱セットでの形態固定効果により2層構造
が完璧に保たれた最終製品が得られ、2層構造による吸
汗性能の優れた製品とすることができる。この時最外周
のポリエステルの断面は複合糸の外周方向に偏平である
ことが内部のポリアミド成分を隠蔽する意味より好まし
く隠蔽効果を考慮すると偏平度は1.5以上であること
が必要である。1.5未満になると隠蔽度が劣るばかり
か2層構造の崩れ易さにもつながる。
The yarn of the present invention forms a complete two-layer structure in the spinning process, and is subjected to yarn making, cloth making, scouring, and heat setting with the form fixed by the elution component, and then the elution component is eluated to elute the elution component. The final product in which the two-layer structure is perfectly maintained by the binding force and the effect of fixing the form by heat setting can be obtained, and the product having excellent sweat absorption performance by the two-layer structure can be obtained. At this time, it is preferable that the outermost peripheral polyester has a flat cross section in the outer peripheral direction of the composite yarn in order to conceal the internal polyamide component, and in view of the concealment effect, the flatness must be 1.5 or more. If it is less than 1.5, not only is the hiding power poor, but the two-layer structure is likely to collapse.

【0009】本発明の複合糸に用いるポリアミドには2
つの欠点がある。1つは複合するポリエステルと染色性
を異にし、ポリエステルの染まる分散染料で染めた場
合、ポリエステルとポリアミドで色目が異なり、色目を
合わせるためには多大な経費と労力が必要である。もう
1つはポリエステルに比べ耐光性に劣る点であり、光に
対して変耐色し易い。また吸湿性をあげるためポリアミ
ドにアクリル酸をグラフト重合すると僅かながら耐光性
に悪影響する。このためポリエステルとポリアミドを複
合する場合は複合糸の外周をポリエステルで覆い、複合
糸の内部にポリアミドを配し、ポリエステルで内部のポ
リアミドを完全に隠蔽することにより前記欠点を排除す
ることが出来る。また外周に配したポリエステルに無機
や有機の微細孔形成剤を混入し、海成分をアルカリ溶液
で溶出する際に外周のポリエステル繊維の1部を溶出し
繊維表面に微細孔を形成すると吸汗能も向上し、ドライ
な触感をも付与しうることよりより好ましい。本発明に
用いる海成分は溶解性の大きいポリマーであり、例えば
イソフタル酸骨格を有するジカルボン酸成分を全酸成分
に対して2.0モル以上含む改質されたポリエチレンテ
レフタレートに、ポリアルキレングリコールを6.0〜
20重量%メルトブレンドしたアルカリ易溶出性ポリエ
ステルが挙げられる。
The polyamide used in the composite yarn of the present invention has 2
There are two drawbacks. One is that the dyeability is different from that of the composite polyester, and when dyed with a disperse dye that dyes polyester, the colors of polyester and polyamide are different, and great expense and labor are required to match the colors. The other is that it is inferior in light resistance to polyester, and is easily discolored and resistant to light. Further, when acrylic acid is graft-polymerized with polyamide in order to improve the hygroscopicity, the light resistance is slightly adversely affected. Therefore, when the polyester and the polyamide are compounded, the above-mentioned drawbacks can be eliminated by covering the outer periphery of the composite yarn with the polyester, disposing the polyamide inside the composite yarn, and completely hiding the internal polyamide with the polyester. Also, by mixing an inorganic or organic fine pore-forming agent into the polyester placed on the outer circumference, and elution of sea components with an alkaline solution, a part of the polyester fiber on the outer circumference is eluted to form fine pores on the fiber surface, which also has a sweat absorbing ability. It is more preferable because it is improved and a dry touch can be imparted. The sea component used in the present invention is a highly soluble polymer. For example, a modified polyethylene terephthalate containing a dicarboxylic acid component having an isophthalic acid skeleton in an amount of 2.0 mol or more based on the total acid component, and a polyalkylene glycol of 6 are used. .0 to
An alkali easily eluting polyester which is melt blended with 20% by weight can be mentioned.

【0010】また吸汗能を考える場合溶出後の複合糸中
の繊維構成数と繊維デニールも重要である。細外周に存
在する島成分の島数(No)はこの島間が気相または液
相の水分の移動道となる点で重要であり、6未満の場合
はこの移動道数が不足し、吸汗性能が充分でない。また
内層部の島成分の数(Ni)は水分を吸着する速度と量
に関係し多い方が好ましいが、複合糸としての総デニー
ルや紡糸ノズル構造や加工費用を考えると30が限界で
ある。また島成分の繊度も同様の意味で重要である。最
外周に存在する島成分の繊維デニール(do)は3デニ
ール以下であることが必要であり、3デニールを越える
と複合糸全体が硬くなり衣料用途に不向きとなる。内層
の島成分の繊維デニール(di)は吸汗性能を上げる意
味合いと貯気相の細分化の意味合いで細い方が好ましい
が出来る布帛の張り腰の観点より0.2デニールが限界
である。又、ポリエステルおよびまたはポリアミド繊維
中に顔料、安定剤改質剤を含有させる公知技術を併用う
ることもできる。また複合繊維間に収縮差を付与し異収
縮混繊糸として利用することもできる。
Further, when considering the sweat absorbing ability, the number of fiber constituents and the fiber denier in the composite yarn after elution are also important. The number of islands (No) of the island component existing in the narrow outer circumference is important in that the water between the islands becomes a migration path for water in the gas phase or liquid phase. If it is less than 6, this migration path is insufficient and sweat absorption performance is low. Is not enough. The number of island components (Ni) in the inner layer is preferably large in relation to the rate and amount of water adsorption, but 30 is the limit when considering the total denier of the composite yarn, the spinning nozzle structure and the processing cost. The fineness of the island component is also important in the same sense. The fiber denier (do) of the island component present in the outermost circumference needs to be 3 denier or less, and if it exceeds 3 denier, the entire composite yarn becomes hard and unsuitable for clothing use. The fiber denier (di) of the island component of the inner layer is preferably thin from the standpoint of enhancing sweat absorption performance and subdividing the gas storage phase, but 0.2 denier is the limit from the standpoint of the fabric tension. Further, it is possible to use a known technique of incorporating a pigment and a stabilizer modifier into the polyester and / or polyamide fiber. Further, it is also possible to impart a shrinkage difference between the composite fibers and use it as a heterogeneous shrinkage mixed yarn.

【0011】[0011]

【実施例】以下に、実施例を用いて本発明を詳述する。EXAMPLES The present invention will be described in detail below with reference to examples.

【0012】実施例1 固有粘度(30℃ フェノール/テトラクロルエタン=
6/4の溶媒で測定)が0.60で平均等価球径が0.
3μmのカオリナイトを2重量%含有したポリエステル
(ポリマーA)を最外周島に配し、相対粘度(30℃
濃硫酸で測定)が2.5のナイロン6(ポリマーB)を
内層島に、ポリエステルにイソフタル酸成分を10モル
%共重合したポリエステルにポリエチレングリコール
(平均分子量が20,000 )を10重量%メルトブレンド
したポリマー(ポリマーC)を海成分として用い、図1
に示す海島型の複合繊維を得た。紡糸温度は280℃で
紡糸ノズルは特開昭57−29605号公報に記載のノ
ズルを最外周の島成分と内層の島成分とが別々のポリマ
ーパスにより別々のギャーポンプより供給できるように
改造したもので複合繊維として4フィラメントを吐出す
るノズルを用いた。各々の吐出量はポリマーAは10.
4g/ノズル・分、ポリマーBは13.0g/ノズル・
分、ポリマーCは9.5g/ノズル・分とし1300m
/分で巻き取った。同未延伸をホットローラー温度を8
0℃、ホットプレート温度を150℃として3倍に延伸
し72デニール4フィラメントの延伸糸を得た。同糸を
用いインターロック編み地とした後、精練、プリセット
をした。その後30g/lの苛性ソーダ溶液で90℃で
処理し、30重量%減量し、中和水洗処理した。この試
料を液体窒素で凍結破断し、縦断面を走査型電子顕微鏡
にて観察したところ図1に示す断面形態が完全に保持さ
れていた。
Example 1 Intrinsic viscosity (30 ° C. phenol / tetrachloroethane =
(Measured in 6/4 solvent) is 0.60 and the average equivalent spherical diameter is 0.
Polyester containing 2% by weight of 3 μm kaolinite (Polymer A) was placed on the outermost island, and the relative viscosity (30 ° C.
Nylon 6 (polymer B) (measured with concentrated sulfuric acid) of 2.5 was melt-blended with 10% by weight of polyethylene glycol (average molecular weight: 20,000) in the inner layer island, and polyester in which 10 mol% of isophthalic acid component was copolymerized with polyester. Using a polymer (Polymer C) as a sea component, Fig. 1
The sea-island type composite fiber shown in was obtained. The spinning temperature was 280 ° C., and the spinning nozzle was modified from the nozzle described in JP-A-57-29605 so that the island component in the outermost periphery and the island component in the inner layer could be supplied from different gear pumps by different polymer passes. A nozzle for discharging 4 filaments as the composite fiber was used. The discharge amount of each polymer A was 10.
4 g / nozzle min, Polymer B is 13.0 g / nozzle
Min, Polymer C is 9.5g / nozzle / min and 1300m
It was wound up at a speed of about 1 minute. Same unstretching with hot roller temperature 8
It was drawn 3 times at 0 ° C. and a hot plate temperature of 150 ° C. to obtain a drawn yarn of 72 denier 4 filaments. After interlock knitting using the same yarn, it was scoured and preset. Then, the mixture was treated with a 30 g / l caustic soda solution at 90 ° C., reduced by 30% by weight, and washed with neutralized water. When this sample was freeze-fractured with liquid nitrogen and the vertical cross section was observed with a scanning electron microscope, the cross-sectional morphology shown in FIG. 1 was completely retained.

【0013】また走査型電子顕微鏡で1000倍に拡大
した断面写真より断面積を算出し、求めた繊維デニール
は外周繊維が1.0デニール6フィラメント、内層繊維
が0.57デニール13フイラメントであった。また外
周繊維の偏平率を同写真より求めた結果、2.32であ
った。この試料を次の方法で吸水性を評価した。試料を
120℃×3時間で乾燥し試料の重量を計測後、20
℃、65%RHに調湿した恒温室に12時間放置した
後、再度試料を計測して重量の増加分を算出し、元の試
料重量に対する増加率で吸湿率とした。又、布帛を水平
面に広げ0.5ccの水滴を5cmの高さより滴下し、
布帛中に吸収されるまでの時間を計測し、吸水速度を相
対比較で1から5級に層別した。(5級の方が良好)同
時に完全に吸収後、3分後に吸水面を指先で触れ、湿潤
感を相対的に判断した。その結果を表1に示した。ポリ
エステル100%の場合に比べ吸湿性の改良が認められ
た。
Further, the cross-sectional area was calculated from a cross-sectional photograph magnified 1000 times with a scanning electron microscope, and the obtained fiber denier was 1.0 denier 6 filaments for the outer peripheral fibers and 0.57 denier 13 filaments for the inner layer fibers. . Further, the flatness ratio of the outer peripheral fibers was 2.32 as a result of obtaining from the same photograph. The water absorption of this sample was evaluated by the following method. After the sample was dried at 120 ° C for 3 hours and the weight of the sample was measured, 20
After the sample was left in a thermostatic chamber at a temperature of 65 ° C and a humidity of 65% for 12 hours, the sample was measured again to calculate the increase in weight, and the rate of increase relative to the original sample weight was taken as the moisture absorption rate. Moreover, the cloth is spread on a horizontal surface and a 0.5 cc water droplet is dropped from a height of 5 cm,
The time until absorption in the fabric was measured, and the water absorption rates were stratified into 1 to 5 grades by relative comparison. (5th grade is better) At the same time, after completely absorbing, 3 minutes later, the water absorption surface was touched with a fingertip to relatively judge the wet feeling. The results are shown in Table 1. An improvement in hygroscopicity was recognized as compared with the case of 100% polyester.

【0014】実施例2 実施例−1で得られた試料を中和水洗後、乾燥し以下の
条件でポリアクリル酸のアル以下の条件でポリアクリル
酸の金属塩をグラフト重合した。 グラフト重合条件 アクリル酸 20g/l 過硫酸アンモニウム 0.5g/l 亜硫酸ナトリウム 3g/l の水溶液で8
0℃×30分処理 グラフト率 5.6% この試料を用い実施例−1と同法で吸湿性を評価し、そ
の結果を表1に示した。グラフト重合により吸湿性はさ
らに改良された。
Example 2 The sample obtained in Example-1 was washed with neutralized water, dried and graft-polymerized with a metal salt of polyacrylic acid under the following conditions. Graft polymerization conditions Acrylic acid 20 g / l Ammonium persulfate 0.5 g / l Sodium sulfite 3 g / l Aqueous solution 8
Treatment at 0 ° C. for 30 minutes Grafting rate: 5.6% Using this sample, the hygroscopicity was evaluated by the same method as in Example-1, and the results are shown in Table 1. The hygroscopicity was further improved by the graft polymerization.

【0015】比較例1 ポリマーBを酸化チタンを0.5%含有するポリエステ
ル(フェノール/テトラクロルエタン=6/4の溶媒で
測定した固有粘度が0.63)とする以外は実施例−1
と全く同じ方法で紡糸、延伸、編み立て、精練、アルカ
リ減量処理を実施した。更に実施例−1と同法で吸湿性
を評価し、その結果を表1に示した。吸湿性は認められ
なかった。
Comparative Example 1 Example 1 except that the polymer B was a polyester containing 0.5% of titanium oxide (intrinsic viscosity of 0.63 measured with a solvent of phenol / tetrachloroethane = 6/4).
Spinning, drawing, knitting, scouring, and alkali weight loss treatment were carried out in exactly the same manner as above. Further, the hygroscopicity was evaluated by the same method as in Example-1, and the results are shown in Table 1. No hygroscopicity was observed.

【0016】[0016]

【表1】 [Table 1]

【0017】[0017]

【発明の効果】本発明は疎水性の外周と親水性の内部を
持つ2層構造複合糸を生み出す複合繊維であり、フィラ
メント糸特有の優美さを表現する能力とべと付き感のな
い吸汗能を合わせ持つ布帛を構成するための複合繊維が
提供できる。
INDUSTRIAL APPLICABILITY The present invention is a composite fiber that produces a two-layer structure composite yarn having a hydrophobic outer periphery and a hydrophilic interior, and has the ability to express the elegance peculiar to filament yarn and the sweat absorbing ability without stickiness. It is possible to provide a composite fiber for forming a fabric having a joint.

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

【図1】本発明の複合繊維の断面を示す図である。FIG. 1 is a view showing a cross section of a conjugate fiber of the present invention.

【符号の説明】[Explanation of symbols]

1は外周に配されたポリエステル系繊維、2は内側に配
されたポリアミド繊維、3は海成分を示す。
1 is a polyester fiber arranged on the outer periphery, 2 is a polyamide fiber arranged on the inner side, and 3 is a sea component.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 D06M 11/38 // D06M 14/34 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location D06M 11/38 // D06M 14/34

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 内側島成分として配されたポリアミド繊
維群と、該ポリアミド繊維群を取り囲むように最外周島
成分として配されたポリエステル繊維群と、溶剤に対し
て溶解性の大きいポリマーよりなる海成分からなる複合
繊維であり、該複合繊維中のポリアミド繊維は複合繊維
に対して50重量%以上の割合で存在し、最外周島成分
として配されたポリエステル繊維の断面は偏平度が1.
5以上であり、かつ、最外周に配されたポリエステル繊
維の単糸デニール(do)および繊維本数(No)と内
側に配されたポリアミド繊維の単糸デニール(di)お
よび繊維本数(Ni)が下記(1)式および(2)式を
満足することを特徴とする複合繊維。 3.0≧do>di≧0.2 ・・・・・・・・・・ (1) 6≦No<Ni≦30 ・・・・・・・・・・ (2) (但し、上記偏平度は、長軸長さ/短軸長さをもって表
わす。)
1. A sea composed of a polyamide fiber group disposed as an inner island component, a polyester fiber group disposed as an outermost peripheral island component so as to surround the polyamide fiber group, and a polymer having a high solubility in a solvent. It is a composite fiber composed of components, and the polyamide fiber in the composite fiber is present in a ratio of 50% by weight or more with respect to the composite fiber, and the cross section of the polyester fiber arranged as the outermost peripheral island component has a flatness of 1.
It is 5 or more, and the single yarn denier (do) and the number of fibers (No) of the polyester fiber arranged at the outermost circumference and the single yarn denier (di) and the number of fibers (Ni) of the polyamide fiber arranged inside are A composite fiber satisfying the following formulas (1) and (2). 3.0 ≧ do> di ≧ 0.2 (1) 6 ≦ No <Ni ≦ 30 (2) (However, the above flatness Is expressed as major axis length / minor axis length.)
JP2909393A 1993-02-18 1993-02-18 Water absorbing composite fiber Pending JPH06240516A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2909393A JPH06240516A (en) 1993-02-18 1993-02-18 Water absorbing composite fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2909393A JPH06240516A (en) 1993-02-18 1993-02-18 Water absorbing composite fiber

Publications (1)

Publication Number Publication Date
JPH06240516A true JPH06240516A (en) 1994-08-30

Family

ID=12266745

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2909393A Pending JPH06240516A (en) 1993-02-18 1993-02-18 Water absorbing composite fiber

Country Status (1)

Country Link
JP (1) JPH06240516A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013129213A1 (en) * 2012-02-27 2013-09-06 東レ株式会社 Island-in-sea fiber, combined filament yarn and textile product
CN103572404A (en) * 2012-08-08 2014-02-12 东丽纤维研究所(中国)有限公司 Sea-island composite fiber
EP2746436A1 (en) * 2011-08-11 2014-06-25 Toray Industries, Inc. Islands-in-sea fiber

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2746436A1 (en) * 2011-08-11 2014-06-25 Toray Industries, Inc. Islands-in-sea fiber
JPWO2013021809A1 (en) * 2011-08-11 2015-03-05 東レ株式会社 Umijima Fiber
EP2746436A4 (en) * 2011-08-11 2015-03-11 Toray Industries Islands-in-sea fiber
WO2013129213A1 (en) * 2012-02-27 2013-09-06 東レ株式会社 Island-in-sea fiber, combined filament yarn and textile product
KR20140128960A (en) * 2012-02-27 2014-11-06 도레이 카부시키가이샤 Island-in-sea fiber, combined filament yarn and textile product
JPWO2013129213A1 (en) * 2012-02-27 2015-07-30 東レ株式会社 Kaishima fiber, blended yarn and textile products
US9663876B2 (en) 2012-02-27 2017-05-30 Toray Industries, Inc. Sea-island composite fiber, mixed yarn and fiber product
CN103572404A (en) * 2012-08-08 2014-02-12 东丽纤维研究所(中国)有限公司 Sea-island composite fiber
CN103572404B (en) * 2012-08-08 2016-03-09 东丽纤维研究所(中国)有限公司 A kind of island-in-sea type composite fiber

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