JPH10219532A - Polyester-based combined filament yarn different in shrinkage of yarn - Google Patents

Polyester-based combined filament yarn different in shrinkage of yarn

Info

Publication number
JPH10219532A
JPH10219532A JP9032737A JP3273797A JPH10219532A JP H10219532 A JPH10219532 A JP H10219532A JP 9032737 A JP9032737 A JP 9032737A JP 3273797 A JP3273797 A JP 3273797A JP H10219532 A JPH10219532 A JP H10219532A
Authority
JP
Japan
Prior art keywords
yarn
layer
polyester
shrinkage
alkali
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
JP9032737A
Other languages
Japanese (ja)
Inventor
Tomoyuki Izumi
智之 和泉
Yoshitomo Hatsutori
芳智 服部
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.)
Nippon Ester Co Ltd
Original Assignee
Nippon Ester 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 Nippon Ester Co Ltd filed Critical Nippon Ester Co Ltd
Priority to JP9032737A priority Critical patent/JPH10219532A/en
Publication of JPH10219532A publication Critical patent/JPH10219532A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain a combined filament yarn different in shrinkage of yarn capable of providing a fabric excellent in hygroscopic property and light resistance and having swelling feeling by constituting the yarn of specific polyester-based conjugated yarns, etc., and weaving or knitting the yarns and subjecting the resultant fabric to weight- reducing treatment by alkali. SOLUTION: This polyester-based combined filament yarn different in shrinkage is composed of plural yarns in which single yarn constituting one or more yarns has hygroscopic property. The combined filament yarn has a three layer structure composed of a core layer comprising a thermoplastic resin 3 such as a polyalkylene terephthalate containing 10-50wt.% polyalkylene glycol having 2,000 to 20,000 average molecular weight, a sheath layer comprising an readily alkali-soluble resin 1, and an intermediate layer comprising a polyester resin 2 which is more slightly soluble in alkali than the sheath layer and arranged in the intermediate between the core layer and the sheath layer and satisfies the formula SA<=50 and the formula SA-SB>=5 [SA is boiling water shrinkage factor (%) of the highest shrinkage yarn in combined filament yarn and SB is boiling water shrinkage factor (%) of the lowest yarn in combined filament yarn].

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、製編織してアルカ
リ減量処理することによって、吸湿性(及び耐光性)に
優れ、かつ、膨らみ感を有する布帛となる異収縮混繊糸
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hetero-shrink mixed yarn which is knitted and woven and subjected to an alkali weight reduction treatment to give a fabric having excellent hygroscopicity (and light resistance) and a swelling feeling. .

【0002】[0002]

【従来の技術】ポリエチレンテレフタレート繊維で代表
されるポリエステル繊維は、優れた機械的、化学的特性
を有し、広範な分野において使用されている。しかしな
がら、このようなポリエステル繊維は、疎水性であるた
め、天然繊維と比較して吸湿性が著しく劣り、吸湿性が
要求される分野での利用が大きく制限されている。
2. Description of the Related Art Polyester fibers represented by polyethylene terephthalate fibers have excellent mechanical and chemical properties and are used in a wide range of fields. However, since such polyester fibers are hydrophobic, their hygroscopicity is remarkably inferior to natural fibers, and their use in fields where hygroscopicity is required is greatly restricted.

【0003】従来、ポリエステル繊維に親水性又は吸湿
性を付与しようとする試みが種々なされており、例え
ば、ポリアルキレングリコール又はポリアルキレングリ
コールとスルホン酸金属塩誘導体などの親水化剤を重合
時あるいは紡糸時に配合したポリエステル繊維が提案さ
れている。しかし、これらの親水化剤、特にポリアルキ
レングリコールは、エーテル結合を有するために、耐光
性が非常に悪く、用途によっては使用できないという問
題があった。
Conventionally, various attempts have been made to impart hydrophilicity or hygroscopicity to polyester fibers. For example, a polyalkylene glycol or a hydrophilizing agent such as a polyalkylene glycol and a metal sulfonic acid derivative is polymerized or spun. Sometimes blended polyester fibers have been proposed. However, these hydrophilizing agents, particularly polyalkylene glycols, have an ether bond, and therefore have a very poor light resistance and cannot be used depending on the application.

【0004】これを解決するために、これら親水化剤を
含むポリマーを芯成分とした複合繊維が提案されてい
る。親水化剤を含むポリマーを芯成分とすることによ
り、耐光性という点ではある程度の効果が認められる。
しかし、風合いを向上させるために一般的に行われてい
るアルカリ減量処理を施すと、ポリアルキレングリコー
ルが吸水、アルカリ分解することにより芯部が膨張する
ために、鞘部に歪みがかかって繊維表面にひび割れが生
じ、アルカリ溶解性の高い芯部の吸湿成分が溶出してし
まうという問題があった。
[0004] In order to solve this problem, conjugate fibers using a polymer containing a hydrophilizing agent as a core component have been proposed. By using a polymer containing a hydrophilizing agent as the core component, a certain effect can be recognized in light resistance.
However, when a general alkali weight reduction treatment is performed to improve the texture, the polyalkylene glycol absorbs water and undergoes alkali decomposition to expand the core. Cracks occur, and the moisture-absorbing component in the core having high alkali solubility is eluted.

【0005】本発明者らは、この鞘割れの問題を解決す
るものとして、吸湿性を有する熱可塑性樹脂からなる芯
層、アルカリ易溶性樹脂からなる鞘層及び芯層と鞘層と
の中間に配された鞘層よりもアルカリ難溶性のポリエス
テル樹脂からなる中間層の3層構造を有するポリエステ
ル系複合糸を提案した(特願平8−215289号) 。
[0005] The present inventors have solved the problem of sheath cracking by providing a core layer made of a thermoplastic resin having hygroscopicity, a sheath layer made of an alkali-soluble resin, and an intermediate layer between the core layer and the sheath layer. A polyester composite yarn having a three-layer structure of an intermediate layer made of a polyester resin which is less soluble in alkali than the sheath layer is proposed (Japanese Patent Application No. 8-215289).

【0006】[0006]

【発明が解決しようとする課題】本発明は、アルカリ減
量処理による繊維表面のひび割れの問題のない上記のよ
うな3層構造を有するポリエステル系複合糸を少なくと
も一部に用いた、製編織してアルカリ減量処理すること
により、吸湿性(及び耐光性)に優れ、かつ、膨らみ感
を有する布帛となる異収縮混繊糸を提供しようとするも
のである。
SUMMARY OF THE INVENTION The present invention relates to a knitting and weaving method using at least a part of a polyester composite yarn having a three-layer structure as described above, which has no problem of cracking of the fiber surface due to alkali weight reduction treatment. It is an object of the present invention to provide a different shrinkage mixed fiber which is excellent in hygroscopicity (and light resistance) and has a swelling feeling by alkali reduction treatment.

【0007】[0007]

【課題を解決するための手段】本発明は、上記課題を解
決するもので、その要旨は、次の通りである。複数の糸
条で構成されたポリエステル系異収縮混繊糸であって、
複数の糸条のうち少なくとも一つの糸条を構成する単糸
が吸湿性を有する熱可塑性樹脂からなる芯層、アルカリ
易溶性樹脂からなる鞘層及び芯層と鞘層との中間に配さ
れた鞘層よりもアルカリ難溶性のポリエステル樹脂から
なる中間層の3層構造を有するポリエステル系複合糸か
らなるものであり、下記式〜を満足することを特徴
とする異収縮混繊糸。 SA≦50 SA−SB≧5 ここで、SA は混繊糸における最高収縮糸条の沸水収縮
率(%)、SB は混繊糸における最低収縮糸条の沸水収
縮率(%)を示す。
The present invention solves the above-mentioned problems, and the gist thereof is as follows. Polyester hetero-shrinkage mixed fiber yarn composed of a plurality of yarns,
The single yarn constituting at least one of the plurality of yarns is disposed between the core layer made of a thermoplastic resin having hygroscopicity, the sheath layer made of an alkali-soluble resin, and the core layer and the sheath layer. A hetero-shrink mixed yarn comprising a polyester-based composite yarn having a three-layer structure of an intermediate layer made of a polyester resin which is less soluble in alkali than the sheath layer, and satisfying the following formulas (1) to (4). SA ≦ 50 SA−SB ≧ 5 Here, SA indicates the boiling water shrinkage (%) of the highest shrinkable yarn in the mixed fiber, and SB indicates the boiling water shrinkage (%) of the lowest shrinkable yarn in the mixed yarn.

【0008】[0008]

【発明の実施の形態】以下、本発明について詳細に説明
する。本発明においては、混繊糸を構成する複数の糸条
のうち少なくとも一つの糸条として、上記のような特定
の3層構造を有するポリエステル系複合糸を用いる。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. In the present invention, a polyester-based composite yarn having a specific three-layer structure as described above is used as at least one of a plurality of yarns constituting the mixed fiber yarn.

【0009】3層構造を有するポリエステル系複合糸に
おいて、芯層を構成する吸湿性を有する熱可塑性樹脂と
しては、平均分子量2000〜20000 のポリアルキレングリ
コールを10〜50重量%、好ましくは15〜35重量%含有さ
せたポリアルキレンテレフタレートが、極めて高い吸湿
性を示し、加えて紡糸、延伸性が良好であり、コスト的
にも有利であるため、好ましく用いられる。 (なお、
「ポリアルキレングリコール」には、末端をエーテル化
したものやエステル化したものも含まれる。) ポリアル
キレングリコールの分子量があまり小さいと十分な吸湿
性が発現せず、逆に大きすぎると紡糸時の操業性が著し
く低下するため、好ましくない。また、ポリアルキレン
グリコールの含有量が少ないと十分な吸湿性が発現せ
ず、逆に多すぎると操業性が著しく低下するため、好ま
しくない。加えて、5−ナトリウムスルホイソフタル酸
のようなスルホン酸塩基を有する化合物を共重合すると
吸湿性の一層良好なものとすることができる。この場
合、この共重合成分の量は、全酸成分の10モル%以下と
することが望ましく、この共重合成分の量があまり多い
と、製糸性が低下するため、好ましくない。
In the polyester composite yarn having a three-layer structure, the moisture-absorptive thermoplastic resin constituting the core layer is a polyalkylene glycol having an average molecular weight of 2,000 to 20,000, 10 to 50% by weight, preferably 15 to 35% by weight. Polyalkylene terephthalate in which the amount of polyalkylene terephthalate is contained by weight is very high because it exhibits extremely high hygroscopicity, has good spinning and drawing properties, and is advantageous in terms of cost. (In addition,
The “polyalkylene glycol” includes those having a terminal etherified or esterified. If the molecular weight of the polyalkylene glycol is too small, sufficient hygroscopicity is not exhibited, and if it is too large, the operability during spinning is remarkably reduced, which is not preferable. On the other hand, if the content of the polyalkylene glycol is small, sufficient hygroscopicity is not exhibited, and if it is too large, the operability is remarkably reduced, which is not preferable. In addition, when a compound having a sulfonic acid group such as 5-sodium sulfoisophthalic acid is copolymerized, the hygroscopicity can be further improved. In this case, the amount of the copolymer component is desirably 10 mol% or less of the total acid components. If the amount of the copolymer component is too large, the spinnability deteriorates.

【0010】また、中間層を形成するポリエステルとし
ては、ポリアルキレンテレフタレート、具体的には、ポ
リエチレンテレフタレート (PET) 及びポリブチレン
テレフタレートが好ましい。ポリアルキレンテレフタレ
ートは、アルカリ溶解性があまり大きくならない範囲
で、少量の共重合成分を含有していてもよく、共重合成
分としては、5−ナトリウムスルホイソフタル酸、イソ
フタル酸、無水フタル酸、ナフタレンジカルボン酸など
の芳香族ジカルボン酸成分、アジピン酸、セバシン酸な
どの脂肪族ジカルボン酸成分、ジエチレングリコール、
プロピレングリコール、 1,4−シクロヘキサンジメタノ
ール、ペンタエリスリトール、ビスフェノールAやビス
フェノールSのアルキレンオキシド付加物などのジオー
ル成分、4−ヒドロキシ安息香酸、ε−カプロラクトン
などのヒドロキシカルボン酸成分が挙げられる。
As the polyester forming the intermediate layer, polyalkylene terephthalate, specifically, polyethylene terephthalate (PET) and polybutylene terephthalate are preferable. The polyalkylene terephthalate may contain a small amount of a copolymer component as long as the alkali solubility is not so large. Examples of the copolymer component include 5-sodium sulfoisophthalic acid, isophthalic acid, phthalic anhydride, and naphthalenedicarboxylic acid. Aromatic dicarboxylic acid component such as acid, adipic acid, aliphatic dicarboxylic acid component such as sebacic acid, diethylene glycol,
Examples include diol components such as propylene glycol, 1,4-cyclohexanedimethanol, pentaerythritol, alkylene oxide adducts of bisphenol A and bisphenol S, and hydroxycarboxylic acid components such as 4-hydroxybenzoic acid and ε-caprolactone.

【0011】また、鞘層は、アルカリ減量処理によって
溶出除去されるものであり、鞘層を構成するアルカリ易
溶性樹脂は、中間層のポリエステルよりもアルカリに対
する溶解速度が2倍以上大きいものが好ましい。このよ
うなアルカリ易溶性樹脂の具体例としては、5−ナトリ
ウムスルホイソフタル酸のようなスルホン酸金属塩を2.
5モル%以上共重合した共重合PETや、スルホン酸金
属塩とポリアルキレングリコールとを共重合した共重合
PETなどが挙げられる。
The sheath layer is eluted and removed by an alkali weight reduction treatment, and the alkali-soluble resin constituting the sheath layer preferably has a dissolution rate in alkali at least twice as high as that of the polyester in the intermediate layer. . Specific examples of such an alkali-soluble resin include metal sulfonates such as 5-sodium sulfoisophthalic acid.
Copolymerized PET obtained by copolymerizing 5 mol% or more, and copolymerized PET obtained by copolymerizing a metal sulfonate and a polyalkylene glycol are exemplified.

【0012】3層構造複合糸において、芯層と中間層と
の割合は、容積比で15/85〜85/15の範囲にすることが
望ましい。芯層の比率がこれよりも小さいと吸湿性に劣
り、一方、中間層の比率がこれよりも小さいとアルカリ
減量処理時に中間層に割れが生じ、好ましくない。
In the three-layer composite yarn, the ratio between the core layer and the intermediate layer is desirably in the range of 15/85 to 85/15 by volume. If the ratio of the core layer is smaller than this, the hygroscopicity is inferior. On the other hand, if the ratio of the intermediate layer is smaller than this, cracks occur in the intermediate layer during alkali reduction treatment, which is not preferable.

【0013】一方、鞘層の割合は、容積比率で繊維全体
の30〜10%の範囲にすることが望ましい。鞘層は、アル
カリ減量処理によって溶出除去するものであるから、こ
の比率をあまり大きくするとコストが高くなって、好ま
しくない。一方、アルカリ減量処理は、布帛の風合いを
向上させるもので、一般に20重量%程度の減量が有効で
あり、鞘層の比率があまり小さいと中間層及び芯層に影
響を与えることなしにアルカリ減量処理を行うことがで
きない。
On the other hand, the ratio of the sheath layer is desirably in the range of 30 to 10% by volume of the whole fiber. Since the sheath layer is to be eluted and removed by the alkali weight reduction treatment, if this ratio is too large, the cost increases, which is not preferable. On the other hand, the alkali weight reduction treatment is intended to improve the texture of the fabric. Generally, a weight loss of about 20% by weight is effective. If the ratio of the sheath layer is too small, the alkali weight loss is not affected without affecting the intermediate layer and the core layer. Processing cannot be performed.

【0014】さらに、3層構造複合糸において、中間層
及び/又は芯層に酸化セリウムとタルク又は酸化セリウ
ムとシリカとからなり、表面が不定形シリカで被覆され
た粒子(耐光剤粒子)を含有させると耐光性を向上させ
ることができて好ましい。このような耐光剤粒子として
は、平均粒子径が 0.1〜3.0 μmのものが好ましく、日
本無機化学工業社から「セリガード」の商品名で市販さ
れているものを使用することができる。
Further, in the three-layer composite yarn, the intermediate layer and / or the core layer contains particles (light-fasting agent particles) composed of cerium oxide and talc or cerium oxide and silica, the surfaces of which are coated with amorphous silica. This is preferable because light resistance can be improved. As such light stabilizer particles, those having an average particle diameter of 0.1 to 3.0 μm are preferable, and those commercially available from Nippon Inorganic Chemical Industry Co., Ltd. under the trade name of “Serigard” can be used.

【0015】耐光剤粒子の添加量は、芯層あるいは中間
層の樹脂に対し0.05〜5重量%、好ましくは 0.1〜1重
量%とするのが適当である。この添加量が0.05重量%未
満であると優れた耐光性が得られず、5重量%を超える
と粒子が凝集しやすくなって紡糸操業性を悪化させるば
かりか、糸条の色調を悪化させる。
The amount of the light stabilizer particles to be added is suitably 0.05 to 5% by weight, preferably 0.1 to 1% by weight, based on the resin of the core layer or the intermediate layer. If the amount is less than 0.05% by weight, excellent light resistance cannot be obtained, and if it exceeds 5% by weight, the particles tend to agglomerate, deteriorating the spinning operability and deteriorating the color of the yarn.

【0016】複合糸の複合形態は、アルカリ減量処理に
よって中間層にひび割れが生じなければ、同心型、偏心
型のいずれでもよく、多芯型でもよい。また、繊維の断
面形状は、円形の他、三角、偏平、多葉型などの異形断
面でもよい。さらに芯層の内部に中空部を設けることも
可能である。
The composite form of the composite yarn may be any of a concentric type, an eccentric type, and a multifilament type as long as the intermediate layer is not cracked by the alkali weight reduction treatment. Further, the cross-sectional shape of the fiber may be an irregular cross-section such as triangular, flat, or multi-leaf type in addition to the circular shape. Further, a hollow portion can be provided inside the core layer.

【0017】図面は、3層構造の複合糸〔各図の
(イ)〕及びそれをアルカリ減量処理して得られる2層
構造の複合糸〔各図の(ロ)〕の横断面を模式的に示す
図であり、図1は同心型、図2は偏心型、図3は多芯型
の例を示す。図面において、1はアルカリ易溶性樹脂
(鞘層)、2はポリエステル樹脂(中間層)、3は吸湿
性を有する熱可塑性樹脂(芯層)を示す。
The drawing is a schematic cross-sectional view of a three-layer composite yarn ((a) in each drawing) and a two-layer composite yarn ((b) in each drawing) obtained by subjecting it to an alkali reduction treatment. 1 shows an example of a concentric type, FIG. 2 shows an example of an eccentric type, and FIG. 3 shows an example of a multi-core type. In the drawings, 1 denotes an alkali-soluble resin (sheath layer), 2 denotes a polyester resin (intermediate layer), and 3 denotes a thermoplastic resin (core layer) having hygroscopicity.

【0018】本発明の混繊糸は、上記のような3層構造
複合糸を20重量%以上、好ましくは40重量%以上を用い
て構成する。3層構造複合糸の割合は、要求される吸湿
性、ドレープ性、ドライ感などの程度に応じて適宜選定
すればよい。他の糸条を混用する場合、その糸条として
は、通常のポリエステル繊維糸条、例えば、PET繊維
糸条、染色性などを改良するための共重合成分を含有し
た共重合PET繊維糸条が用いられる。
The mixed fiber of the present invention is constituted by using the above-described three-layer composite yarn in an amount of 20% by weight or more, preferably 40% by weight or more. The proportion of the three-layer composite yarn may be appropriately selected according to the required degree of hygroscopicity, drape, dryness and the like. When other yarns are mixed, as the yarns, ordinary polyester fiber yarns, for example, PET fiber yarns, copolymerized PET fiber yarns containing a copolymerization component for improving dyeability and the like are used. Used.

【0019】本発明の混繊糸は、前記式及びを満足
することが必要である。すなわち、最高収縮糸条の沸水
収縮率SA が50%以下であり、SA と最低収縮糸条の沸
水収縮率SB との差が5%以上であることが必要であ
る。SA が50%以上であると布帛にしたとき、その風合
いが硬くなり、好ましくない。また、SA とSB との差
が5%未満であると十分な膨らみ感を有する布帛とする
ことができない。
It is necessary that the mixed fiber of the present invention satisfies the above formulas. That is, the boiling water shrinkage ratio SA of the highest shrinkable yarn must be 50% or less, and the difference between SA and the boiling water shrinkage ratio SB of the lowest shrinkable yarn must be 5% or more. When the SA is 50% or more, when the fabric is formed, the texture becomes hard, which is not preferable. If the difference between SA and SB is less than 5%, a fabric having a sufficient swelling feeling cannot be obtained.

【0020】最大収縮糸条と最低収縮率糸条との比率
は、重量比で1/9〜9/1、好ましくは3/7〜7/
3とするのが適当であり、両糸条の合計が混繊糸の50重
量%以上、好ましくは70重量%以上となるようにするこ
とが望ましい。そして、これらの範囲内で、要求される
膨らみ感の度合いに応じて適宜これらの割合を選定すれ
ばよい。なお、中間収縮糸条が存在する場合、その沸水
収縮率は特に限定されない。
The ratio of the maximum shrinkage yarn to the minimum shrinkage yarn is 1/9 to 9/1, preferably 3/7 to 7 / by weight ratio.
It is appropriate to set it to 3, and it is desirable that the total of both yarns is 50% by weight or more, preferably 70% by weight or more of the mixed fiber. Then, within these ranges, these ratios may be appropriately selected according to the required degree of swelling. When the intermediate shrinkage yarn is present, its boiling water shrinkage is not particularly limited.

【0021】次に、本発明の異収縮混繊糸の製法につい
て説明する。本発明の異収縮混繊糸は、前記のような3
層構造複合糸と必要に応じて通常のポリエステル繊維糸
条とを用い、所定の沸水収縮率の糸条を混繊することに
より製造することができるが、次のような延伸混繊法を
採用すると効率的に製造することができる。
Next, a method for producing the different shrinkage mixed fiber yarn of the present invention will be described. The hetero-shrinkage mixed fiber of the present invention has the 3
It can be manufactured by using a layered composite yarn and, if necessary, a normal polyester fiber yarn, and mixing yarn having a predetermined boiling water shrinkage ratio. Then, it can be manufactured efficiently.

【0022】すなわち、まず、常法によって前記のよう
な3層構造複合糸を溶融紡糸し、未延伸糸を巻き取る。
次いで、この3層構造複合糸からなる未延伸糸同士又は
3層構造複合糸からなる未延伸糸と常法の溶融紡糸で得
られた通常のポリエステル繊維糸条からなる未延伸糸と
を同時に延伸機に供給し、それぞれの未延伸糸を異なる
熱処理条件で延伸、熱処理した後、混繊し、異収縮混繊
糸を得る。混繊の方法は、特に限定されるものではな
く、引き揃えでもよいが、流体交絡処理を施して混繊す
る方法が好ましい。
That is, first, the above-described three-layer composite yarn is melt-spun by a conventional method, and an undrawn yarn is wound.
Next, the undrawn yarns composed of the three-layered composite yarn or the undrawn yarns composed of the three-layered composite yarn and the undrawn yarn composed of a normal polyester fiber yarn obtained by a conventional melt spinning are simultaneously drawn. The unstretched yarns are supplied to a machine, stretched and heat-treated under different heat treatment conditions, and then mixed to obtain a different shrink mixed yarn. The method of fiber mixing is not particularly limited, and may be aligned, but a method of performing fiber entanglement and mixing the fibers is preferable.

【0023】本発明の異収縮混繊糸は、必要に応じて仮
撚加工や撚糸加工を施した後、製編織して布帛とし、ア
ルカリ減量処理が施される。アルカリ減量処理すると、
3層構造の複合糸は、鞘層が溶出除去され、吸湿性の優
れた2層構造の複合糸となり、吸湿性を有する布帛が得
られる。そして、3層構造の複合糸は、アルカリ減量処
理しても鞘部のみが減量されて、吸湿成分が膨潤してひ
び割れしないので、吸湿成分が糸中に保持され、優れた
吸湿性を有する布帛となる。
The hetero-shrinkage mixed fiber of the present invention is subjected to false twisting and twisting as required, and then knitted and woven into a fabric, which is subjected to an alkali weight reduction treatment. When the alkali weight loss treatment,
The three-layered composite yarn has the sheath layer eluted and removed, and becomes a two-layered composite yarn having excellent hygroscopicity. Thus, a fabric having hygroscopicity can be obtained. The composite yarn having a three-layer structure has only the sheath portion reduced even when subjected to alkali weight reduction treatment, and the moisture-absorbing component swells and does not crack, so that the moisture-absorbing component is retained in the yarn, and the fabric has excellent moisture absorption. Becomes

【0024】アルカリ減量処理は、ポリエステル繊維の
アルカリ減量加工の常法に従って、水酸化ナトリウム水
溶液を用いて行えばよい。
The alkali weight reduction treatment may be performed using an aqueous sodium hydroxide solution in accordance with a conventional method for alkali weight reduction processing of polyester fibers.

【0025】また、異収縮混繊糸からなる布帛は、精
練、アルカリ減量処理、染色などの工程で熱処理を施す
と収縮差によって糸長差が生じ、この糸長差により糸条
間に空隙部が形成され、布帛に膨らみ感や軽量感が付与
される。
Further, when heat treatment is performed in the steps of scouring, alkali reduction treatment, dyeing, etc., the yarn made of the different shrinkage mixed yarns causes a difference in yarn length due to a difference in shrinkage. Is formed, and a swelling feeling and a lightweight feeling are imparted to the fabric.

【0026】[0026]

【実施例】次に、実施例によって本発明を具体的に説明
する。なお、実施例及び比較例における特性値などの測
定、評価法は次のとおりである。 (1) 極限粘度(〔η〕) フェノールと四塩化エタンとの等重量混合物を溶媒とし
て、温度20℃で測定した。 (2) アルカリ溶解性 ポリマー5gを20重量%水酸化ナトリウム水溶液で70℃
で2時間処理した際の重量変化より求めた減量率を指標
とした。 (3) 沸水収縮率 異収縮混繊糸をパッケージから引き出し、高収縮性糸条
と低収縮性糸条に分割してそれぞれ検尺機で綛取りし、
1/30g/dの荷重下で糸長L0 を測定し、次いで、無荷
重下で沸水中に30分間浸漬を行って糸条を収縮させ、風
乾後、再度1/30g/dの荷重下で収縮後の長さL1 を測
定し、沸水収縮率を次式で算出する。 沸水収縮率(%)=〔(L0−L1)/L0 〕×100 (4) 繊維表面の割れの評価 織物を分解して複合糸を取り出し、繊維断面を薄片状に
サンプリングし、顕微鏡により、単糸ごとに割れの有無
を観察し、割れのある単糸の本数の割合により、次の基
準で評価した。 ○: 0%、 △:15%未満、 ×:15%以上 (5) 膨らみ感 仕上げセット後の織物の官能試験により、次の3段階で
評価した。 ○: 極めて良好、 △:良好、 ×:不良 (6) 耐光性 JIS L-0841-74 に準じて染色耐光堅牢度を測定した。 (7) 吸湿性 織物を25℃、60%RHで調湿して重量W0 を測定する。
次いで、この織物を2トルの減圧下、80℃で6時間乾燥
し、34℃×90%RHに設定した恒温恒湿槽に6時間放置
した後、重量W1 を測定する。そして、次式で吸湿率を
算出する。 吸湿率(%)=〔(W1−W0)/W0 〕×100
Next, the present invention will be described specifically with reference to examples. The methods for measuring and evaluating characteristic values and the like in Examples and Comparative Examples are as follows. (1) Intrinsic viscosity ([η]) Measured at a temperature of 20 ° C. using an equal weight mixture of phenol and ethane tetrachloride as a solvent. (2) Alkali solubility 5 g of polymer at 70 ° C. with a 20% by weight aqueous sodium hydroxide solution
The weight loss rate obtained from the change in weight when treated for 2 hours was used as an index. (3) Boiling water shrinkage ratio Different shrinkage mixed fiber yarn is pulled out from the package, divided into high shrinkage yarn and low shrinkage yarn, and skeined with a measuring machine.
The yarn length L 0 is measured under a load of 1/30 g / d, then immersed in boiling water under no load for 30 minutes to shrink the yarn, air-dried, and then again under a load of 1/30 g / d. in the length L 1 after shrinkage was measured to calculate the boiling water shrinkage percentage by the following equation. Boiling water shrinkage (%) = [(L 0 −L 1 ) / L 0 ] × 100 (4) Evaluation of cracks on fiber surface The woven fabric is disassembled to take out the composite yarn, and the fiber cross section is sampled into a flaky shape, and the microscope is used. The presence or absence of cracks was observed for each single yarn, and the following criteria were used to evaluate the ratio of the number of single yarns having cracks. :: 0%, △: less than 15%, ×: 15% or more (5) Feeling of swelling The woven fabric after the finishing set was evaluated by the following three grades. :: extremely good, Δ: good, ×: bad (6) Light fastness The light fastness of dyeing was measured according to JIS L-0841-74. (7) Hygroscopicity The woven fabric is conditioned at 25 ° C. and 60% RH, and the weight W 0 is measured.
Next, the woven fabric is dried at 80 ° C. for 6 hours under a reduced pressure of 2 Torr, left in a thermo-hygrostat set at 34 ° C. × 90% RH for 6 hours, and the weight W 1 is measured. Then, the moisture absorption rate is calculated by the following equation. Moisture absorption (%) = [(W 1 −W 0 ) / W 0 ] × 100

【0027】参考例1 ビス(β−ヒドロキシエチル)テレフタレート及びその
オリゴマーの存在するエステル化反応装置にテレフタル
酸とエチレングリコールとのモル比1/1.6 のスラリー
を連続的に供給し、常圧下、温度 250℃で、滞留時間を
6時間としてエステル化反応を行い、平均重合度 7.5の
エステル化生成物を連続的に得た。このエステル化生成
物36.3kgに平均分子量が8500のポリエチレングリコール
(PEG)を15.0kg添加し、30分間撹拌混合後、「セリ
ガードT−3018」の10重量%エチレングリコール溶液
1.3kg、全酸成分1モルに対し4×10-4モルの三酸化ア
ンチモン及び酢酸ナトリウムの5重量%エチレングリコ
ール溶液 0.5kgを加え、次いで、全酸成分に対し 0.5モ
ル%の5−ナトリウムスルホイソフタル酸のエチレング
リコールエステル(SIP)を加え、徐々に減圧にし
て、最終的に圧力0.5トル、温度 270℃の条件で3時間
重縮合を行った。なお、「セリガードT−3018」は、日
本無機化学工業社の商品名で、酸化セリウムとタルクと
からなる粒子の表面を不定形シリカで被膜したもので、
酸化セリウム:タルク:不定形シリカの重量比が30:5
2:18のものである。得られたポリエステル(ポリマー
Aとする)は、色調が良好で、〔η〕は0.83であった。
ポリマーAの特性値などを表1に示す。
Reference Example 1 A slurry of terephthalic acid and ethylene glycol at a molar ratio of 1 / 1.6 was continuously supplied to an esterification reactor in which bis (β-hydroxyethyl) terephthalate and its oligomer were present, and the mixture was heated at normal pressure and temperature. The esterification reaction was carried out at 250 ° C. with a residence time of 6 hours, and an esterification product having an average degree of polymerization of 7.5 was continuously obtained. To 36.3 kg of this esterified product, 15.0 kg of polyethylene glycol (PEG) having an average molecular weight of 8500 was added and mixed by stirring for 30 minutes, and then a 10% by weight ethylene glycol solution of "Serigard T-3018" was added.
1.3 kg, 0.5 kg of a solution of 4 × 10 -4 mol of antimony trioxide and sodium acetate in a 5% by weight ethylene glycol solution per mol of the total acid component were added, and then 0.5 mol% of 5-sodium sulfo acid was added to the total acid component. Ethylene glycol ester of isophthalic acid (SIP) was added, the pressure was gradually reduced, and finally polycondensation was performed at a pressure of 0.5 torr and a temperature of 270 ° C. for 3 hours. "Serigard T-3018" is a trade name of Nippon Inorganic Chemical Industry Co., Ltd., in which particles made of cerium oxide and talc are coated with amorphous silica.
The weight ratio of cerium oxide: talc: amorphous silica is 30: 5
2:18. The obtained polyester (referred to as polymer A) had a good color tone, and [η] was 0.83.
Table 1 shows the characteristic values of the polymer A and the like.

【0028】参考例2〜8 PEGの分子量と添加量、SIPの添加量及び「セリガ
ードT−3018」の添加量を表1に示した値に変えた以外
は、参考例1と同様にしてポリエステル(ポリマーB〜
Hとする)を得た。ポリマーB〜Hの特性値などを表1
に示す。
Reference Examples 2 to 8 Polyester was prepared in the same manner as in Reference Example 1 except that the molecular weight and the amount of PEG, the amount of SIP added, and the amount of “Serigard T-3018” were changed to the values shown in Table 1. (Polymer B ~
H). Table 1 shows the characteristic values of the polymers B to H.
Shown in

【0029】[0029]

【表1】 [Table 1]

【0030】参考例9〜14 表2示したポリマーの組合せで、芯部/中間層/鞘部の
複合比率(容積比)=65/15/20で同心円型3層構造複
合糸を溶融紡糸し、1400m/分の速度で巻取り、 125d
/18fの未延伸糸a〜fを得た。
Reference Examples 9 to 14 Concentric circular three-layer composite yarns were melt-spun at a composite ratio (volume ratio) of core / intermediate layer / sheath of 65/15/20 using the combinations of polymers shown in Table 2. Winding at 1400m / min, 125d
/ 18f of undrawn yarns a to f were obtained.

【0031】[0031]

【表2】 [Table 2]

【0032】参考例15 芯成分としてポリマーA、鞘成分としてポリマーBを用
い、芯部/鞘部の複合比率(容積比)=80/20で同心円
型2層構造複合糸を溶融紡糸し、1400m/分の速度で巻
取り、 125d/18fの未延伸糸gを得た。
REFERENCE EXAMPLE 15 A concentric double-layered composite yarn was melt-spun at a composite ratio (volume ratio) of core / sheath = 80/20 using polymer A as the core component and polymer B as the sheath component. At a speed of / min to obtain a 125d / 18f undrawn yarn g.

【0033】参考例16 ポリマーB及びポリマーEを用い、単成分糸条を溶融紡
糸し、1400m/分の速度で巻取り、 125d/18fのポリ
マーBを用いた未延伸糸h及びポリマーEを用いた未延
伸糸iを得た。
REFERENCE EXAMPLE 16 A single component yarn was melt-spun using polymer B and polymer E, wound at a speed of 1400 m / min, and undrawn yarn h and polymer E using 125 d / 18 f polymer B were used. The obtained undrawn yarn i was obtained.

【0034】実施例1 未延伸糸aと未延伸糸hとを延伸機に供給し、延伸速度
700m/分、温度80℃、延伸倍率 3.5倍で同時に延伸を
行い、糸条aは50℃の加熱板(処理長50cm)、糸条hは
170℃の加熱板(処理長50cm)に全面接触させて熱処理
してから2つの糸条を合糸し、流体交絡処理を施した
後、異収縮混繊糸を巻取った。この異収縮混繊糸を経糸
及び緯糸に用い、経糸密度 110本/2.54cm、緯糸密度78
本/2.54cmで無撚の平織を製織し、常法に従って、精練
し、次いで、濃度 0.5重量%の水酸化ナトリウム水溶液
により、温度95℃、時間20分の条件でアルカリ減量処理
を行った後、常法に従って、染色及び仕上げセットを行
った。得られた織物は、膨らみ感が良好であり、吸湿率
4.2%、染色耐光堅牢度5級と優れた特性を示した。ま
た、この織物を分解して複合糸を取り出し、複合糸を構
成する単糸36本すべての断面を観察したが、いずれの単
糸も表層にひび割れは発生していなかった。異収縮混繊
糸の沸水収縮率及び織物の評価結果を表3に示す。
Example 1 An undrawn yarn a and an undrawn yarn h are supplied to a drawing machine, and a drawing speed is set.
At the same time, drawing is performed at 700 m / min, at a temperature of 80 ° C., and at a draw ratio of 3.5, yarn a is heated at 50 ° C. (processing length 50 cm) and yarn h is drawn
The whole was brought into contact with a heating plate of 170 ° C. (treatment length: 50 cm) and heat-treated. After that, the two yarns were combined and subjected to a fluid entanglement treatment, and then the hetero-shrinkage mixed fiber was wound. The different shrinkage blended yarn is used for warp and weft, and has a warp density of 110 yarns / 2.54 cm and a weft density of 78.
After weaving an untwisted plain weave at 2.54 cm, scouring according to a conventional method, and then performing an alkali weight reduction treatment with a 0.5% by weight aqueous sodium hydroxide solution at a temperature of 95 ° C. for 20 minutes. The dyeing and finishing set were performed according to a conventional method. The obtained woven fabric has a good swelling feeling and a moisture absorption rate.
4.2%, dyeing light fastness class 5 and excellent properties. Further, the woven fabric was disassembled to take out the composite yarn, and the cross section of all 36 single yarns constituting the composite yarn was observed, but none of the single yarns had any cracks on the surface layer. Table 3 shows the boiling water shrinkage of the different shrinkage mixed fiber and the evaluation results of the woven fabric.

【0035】実施例2〜5 表3に示すように未延伸糸を組合せて延伸機に供給し、
実施例1と同様な条件で延伸し、各糸条の沸水収縮率が
所定の値となるように温度を選定して熱処理した後合糸
し、流体交絡処理を施して異収縮混繊糸とし、これらを
用いて実施例1と同様にして混繊糸織物を得た。異収縮
混繊糸の沸水収縮率及び織物の評価結果を表3に示す。
Examples 2 to 5 As shown in Table 3, undrawn yarns were combined and supplied to a drawing machine.
The yarn is drawn under the same conditions as in Example 1, heat-treated at a selected temperature so that the boiling water shrinkage ratio of each yarn becomes a predetermined value, then conjugated, and subjected to a fluid entanglement treatment to obtain a different shrinkage mixed fiber. Using these, a mixed fiber fabric was obtained in the same manner as in Example 1. Table 3 shows the boiling water shrinkage of the different shrinkage mixed fiber and the evaluation results of the woven fabric.

【0036】実施例6 3種の未延伸糸a、h及びiを延伸機に供給し、実施例
1と同様な条件で延伸し、糸条aは45℃の熱板、糸条h
及びiは 160℃の熱板に全面接触させて熱処理してから
3つの糸条を合糸し、流体交絡処理を施した後、異収縮
混繊糸を巻取った。得られた異収縮混繊糸を用いて実施
例1と同様にして混繊糸織物を得た。異収縮混繊糸の沸
水収縮率及び織物の評価結果を表3に示す。
Example 6 Three kinds of undrawn yarns a, h and i were supplied to a drawing machine and drawn under the same conditions as in Example 1. The yarn a was heated at 45 ° C. and the yarn h
For i and i, the whole was brought into contact with a hot plate at 160 ° C., heat-treated, three yarns were combined, subjected to a fluid entanglement treatment, and then a different shrinkage mixed fiber was wound. A mixed fiber woven fabric was obtained in the same manner as in Example 1 using the obtained different shrinkage mixed fiber. Table 3 shows the boiling water shrinkage of the different shrinkage mixed fiber and the evaluation results of the woven fabric.

【0037】比較例1〜5 表3に示すように未延伸糸を組合せて延伸機に供給し、
実施例1と同様な条件で延伸し、各糸条の沸水収縮率が
所定の値となるように温度を選定して熱処理した後、合
糸し、流体交絡処理を施して異収縮混繊糸とし、これら
を用いて実施例1と同様にして混繊糸織物を得た。異収
縮混繊糸の沸水収縮率及び織物の評価結果を表3に示
す。
Comparative Examples 1 to 5 As shown in Table 3, undrawn yarns were combined and supplied to a drawing machine.
It is stretched under the same conditions as in Example 1, heat-treated at a selected temperature such that the boiling water shrinkage of each yarn becomes a predetermined value, then combined, subjected to a fluid entanglement treatment, and subjected to a different shrinkage mixed fiber. Using these, a mixed fiber fabric was obtained in the same manner as in Example 1. Table 3 shows the boiling water shrinkage of the different shrinkage mixed fiber and the evaluation results of the woven fabric.

【0038】[0038]

【表3】 [Table 3]

【0039】表3から明らかなように、実施例1〜6の
異収縮混繊糸から得られた織物は、繊維表面にひび割れ
がなく、優れた膨らみ感及び吸湿性を有し、耐光性の良
好な織物であった。これに対して、比較例1では、最大
収縮糸条の沸水収縮率が大きすぎたため、織物全体が硬
いものとなり、膨らみ感が出なかった。比較例2では、
糸条間の沸水収縮率差が小さかったため、膨らみ感が出
なかった。比較例3では、3層構造型複合糸の中間層に
鞘部よりアルカリ溶解性の大きいポリマーを使用したた
め、アルカリ減量処理後、繊維表面に割れが発生した。
比較例4では、アルカリ減量処理による繊維表面にひび
割れもなく、耐光性も良好で、膨らみ感のある織物が得
られたが、吸湿性が低いものであった。比較例5では、
吸湿性糸条として2成分芯鞘複合糸を使用したため、ア
ルカリ減量処理により鞘割れが発生した。
As is clear from Table 3, the woven fabrics obtained from the different shrinkage-mixed yarns of Examples 1 to 6 have no cracks on the fiber surface, have excellent swelling and hygroscopic properties, and have light resistance. It was a good fabric. On the other hand, in Comparative Example 1, the boiling water shrinkage rate of the maximum shrinkable yarn was too large, so that the entire woven fabric was hard and no swelling feeling was obtained. In Comparative Example 2,
Since the difference in boiling water shrinkage ratio between the yarns was small, no swelling was obtained. In Comparative Example 3, since a polymer having higher alkali solubility than the sheath portion was used for the intermediate layer of the three-layer structure type composite yarn, cracks occurred on the fiber surface after the alkali weight reduction treatment.
In Comparative Example 4, although the fiber surface was not cracked due to the alkali weight reduction treatment, the light resistance was good, and a woven fabric having a swelling feeling was obtained, but the hygroscopicity was low. In Comparative Example 5,
Since the two-component core-sheath composite yarn was used as the hygroscopic yarn, sheath cracking occurred due to the alkali weight reduction treatment.

【0040】[0040]

【発明の効果】本発明によれば、アルカリ減量処理によ
る繊維表面のひび割れの問題のない3層構造を有するポ
リエステル系複合糸を少なくとも一部に用いた、製編織
してアルカリ減量処理することにより、吸湿性(及び耐
光性)に優れ、かつ、膨らみ感を有する布帛となる異収
縮混繊糸が提供される。
According to the present invention, a polyester-based composite yarn having a three-layer structure having no problem of cracking on the fiber surface due to the alkali weight reduction treatment is used at least in part, and is knitted and woven to carry out the alkali weight reduction treatment. The present invention provides a different shrinkage mixed fiber which is excellent in hygroscopicity (and light resistance) and has a swelling feeling.

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

【図1】本発明における同心型3層構造複合糸(イ)及
びそれをアルカリ減量処理して得られる2層構造複合糸
(ロ)の横断面を模式的に示す図である。
FIG. 1 is a view schematically showing a cross section of a concentric three-layer composite yarn (a) and a two-layer composite yarn (b) obtained by subjecting it to an alkali reduction treatment in the present invention.

【図2】本発明における偏心型3層構造複合糸(イ)及
びそれをアルカリ減量処理して得られる2層構造複合糸
(ロ)の横断面を模式的に示す図である。
FIG. 2 is a diagram schematically showing a cross section of an eccentric type three-layer composite yarn (a) and a two-layer composite yarn (b) obtained by subjecting it to an alkali reduction treatment in the present invention.

【図3】本発明における多芯型3層構造複合糸(イ)及
びそれをアルカリ減量処理して得られる2層構造複合糸
(ロ)の横断面を模式的に示す図である。
FIG. 3 is a view schematically showing a cross section of a multifilament three-layer composite yarn (a) and a two-layer composite yarn (b) obtained by subjecting the multifilament three-layer composite yarn to an alkali weight reduction process.

【符号の説明】[Explanation of symbols]

1 アルカリ易溶性樹脂 2 ポリエステル樹脂 3 吸湿性を有する熱可塑性樹脂 DESCRIPTION OF SYMBOLS 1 Alkali easily soluble resin 2 Polyester resin 3 Moisture-absorbing thermoplastic resin

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 複数の糸条で構成されたポリエステル系
異収縮混繊糸であって、複数の糸条のうち少なくとも一
つの糸条を構成する単糸が吸湿性を有する熱可塑性樹脂
からなる芯層、アルカリ易溶性樹脂からなる鞘層及び芯
層と鞘層との中間に配された鞘層よりもアルカリ難溶性
のポリエステル樹脂からなる中間層の3層構造を有する
ポリエステル系複合糸からなるものであり、下記式〜
を満足することを特徴とする異収縮混繊糸。 SA≦50 SA−SB≧5 ここで、SA は混繊糸における最高収縮糸条の沸水収縮
率(%)、SB は混繊糸における最低収縮糸条の沸水収
縮率(%)を示す。
1. A polyester-based hetero-shrinkage mixed fiber composed of a plurality of yarns, wherein a single yarn constituting at least one of the plurality of yarns is made of a thermoplastic resin having hygroscopicity. It is composed of a polyester-based composite yarn having a three-layer structure of a core layer, a sheath layer composed of an alkali-soluble resin, and an intermediate layer composed of a polyester resin that is less soluble in alkali than the sheath layer disposed between the core layer and the sheath layer. And the following formula:
A different shrinkage mixed fiber yarn characterized by satisfying the following. SA ≦ 50 SA−SB ≧ 5 Here, SA indicates the boiling water shrinkage (%) of the highest shrinkable yarn in the mixed fiber, and SB indicates the boiling water shrinkage (%) of the lowest shrinkable yarn in the mixed yarn.
【請求項2】 3層構造を有するポリエステル系複合糸
の芯層の熱可塑性樹脂が、平均分子量2000〜20000 のポ
リアルキレングリコールを10〜50重量%含有するポリア
ルキレンテレフタレートである請求項1記載の異収縮混
繊糸。
2. The thermoplastic resin of the core layer of the polyester composite yarn having a three-layer structure is a polyalkylene terephthalate containing 10 to 50% by weight of a polyalkylene glycol having an average molecular weight of 2,000 to 20,000. Different shrinkage mixed fiber.
【請求項3】 3層構造を有するポリエステル系複合糸
の芯層及び/又は中間層の樹脂が、酸化セリウムとタル
ク又は酸化セリウムとシリカとからなり、かつ、表面が
不定形シリカで被覆された粒子を0.05〜5重量%含有す
るものである請求項1又は2記載の異収縮混繊糸。
3. The resin of a core layer and / or an intermediate layer of a polyester-based composite yarn having a three-layer structure is made of cerium oxide and talc or cerium oxide and silica, and the surface is coated with amorphous silica. The mixed-shrink mixed fiber according to claim 1 or 2, which contains 0.05 to 5% by weight of particles.
JP9032737A 1997-01-30 1997-01-30 Polyester-based combined filament yarn different in shrinkage of yarn Pending JPH10219532A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9032737A JPH10219532A (en) 1997-01-30 1997-01-30 Polyester-based combined filament yarn different in shrinkage of yarn

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9032737A JPH10219532A (en) 1997-01-30 1997-01-30 Polyester-based combined filament yarn different in shrinkage of yarn

Publications (1)

Publication Number Publication Date
JPH10219532A true JPH10219532A (en) 1998-08-18

Family

ID=12367156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9032737A Pending JPH10219532A (en) 1997-01-30 1997-01-30 Polyester-based combined filament yarn different in shrinkage of yarn

Country Status (1)

Country Link
JP (1) JPH10219532A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019167646A (en) * 2018-03-23 2019-10-03 東レ株式会社 Bulky light-weight multifilament

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019167646A (en) * 2018-03-23 2019-10-03 東レ株式会社 Bulky light-weight multifilament

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