JPH07189119A - Water-absorbing polyamide fiber and its production - Google Patents

Water-absorbing polyamide fiber and its production

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Publication number
JPH07189119A
JPH07189119A JP32423593A JP32423593A JPH07189119A JP H07189119 A JPH07189119 A JP H07189119A JP 32423593 A JP32423593 A JP 32423593A JP 32423593 A JP32423593 A JP 32423593A JP H07189119 A JPH07189119 A JP H07189119A
Authority
JP
Japan
Prior art keywords
fiber
polyamide
water
weight
polyamide fiber
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
JP32423593A
Other languages
Japanese (ja)
Inventor
Akio Takeuchi
昭男 竹内
Tadashi Koyanagi
小柳  正
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP32423593A priority Critical patent/JPH07189119A/en
Publication of JPH07189119A publication Critical patent/JPH07189119A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To obtain a new polyamide fiber having light weight and excellent water-absorbing performance, water-retaining performance and water-releasing performance and free from slimy feeling. CONSTITUTION:This polyamide fiber is characterized in that the single fiber constituting the polyamide fiber is a dense agglomerate of fibrils oriented nearly parallel to the fiber axis. It can be produced by subjecting a fiber obtained by the melt-spinning of a blend polymer composed of 70-50wt.% of a polyamide and 30-50wt.% of a polyester obtained by the copolymerization of a polyethylene terephthalate with 10-30wt.% of a polyethylene glycol, thereby dissolving and removing the copolymerized polyester.

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、スポーツ用途等の衣料
用および吸水敷物用途等の資材用に適した、ポリアミド
系繊維特有のぬめり感を有さず、軽量で、吸水性能、保
水性能、放水性能に優れた新規なポリアミド繊維および
その製造方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is suitable for clothes such as sports and materials for water absorbent rugs, does not have a slimy feeling peculiar to polyamide fibers, is lightweight, and has water absorption performance, water retention performance, and The present invention relates to a novel polyamide fiber having excellent water discharge performance and a method for producing the same.

【0002】[0002]

【従来の技術】ポリアミド系繊維特有のぬめり感を除去
する方法として、ポリアミドに1〜10重量%のポリエ
ステルを均一に混合溶融し、紡糸延伸して得られた混合
繊維をアルカリ金属の水酸化物によって処理し、糸条中
のポリエステルの50〜100重量%を溶出せしめて、
繊維の表面の長さ方向に筋状の微細な凹凸をつける方法
が提案されている(特公昭45−1646号公報)。
2. Description of the Related Art As a method for removing the slimy feeling peculiar to polyamide fibers, 1 to 10% by weight of polyester is uniformly mixed and melted with polyamide, and the mixed fibers obtained by spinning and drawing are mixed with alkali metal hydroxide. To elute 50 to 100% by weight of the polyester in the yarn,
A method has been proposed in which fine streaky irregularities are formed on the surface of a fiber (Japanese Patent Publication No. 45-1646).

【0003】この方法は紡糸時の断糸が多発したり、延
伸時の毛羽断糸などで生産性が極めて悪いので、有機ス
ルホン酸金属塩含有ポリエステルとポリアミドとを混合
紡糸して得た繊維よりポリエステルを溶出除去する方法
が提案されている(特開平2−175965号公報)。
[0003] Since this method has a very poor productivity due to frequent breakage of fibers during spinning and fluff breakage during stretching, the fiber obtained by mixing and spinning a polyester containing an organic sulfonic acid metal salt and a polyamide is A method of eluting and removing polyester has been proposed (JP-A-2-175965).

【0004】[0004]

【発明が解決しようとする課題】しかしながら、上記従
来技術により得られる繊維はその長さ方向に筋状の微細
孔を有するのみであるため、繊維の風合は絹様であり、
吸水性能、保水性能、放水性能も綿を越えることはでき
なかった。本発明は、ポリアミド系繊維特有のぬめり感
を有さず、軽量で、また吸水性能、保水性能、放水性能
に優れた新規なポリアミド繊維およびその製造方法に関
するものである。
However, since the fibers obtained by the above-mentioned prior art only have streak-shaped fine pores in the length direction, the texture of the fibers is silk-like,
The water absorption performance, water retention performance, and water discharge performance could not exceed cotton. TECHNICAL FIELD The present invention relates to a novel polyamide fiber which does not have a slimy feeling peculiar to polyamide-based fibers, is lightweight, and is excellent in water absorption performance, water retention performance, and water discharge performance, and a method for producing the same.

【0005】[0005]

【課題を解決するための手段】本発明者等は上記課題を
解決するために鋭意研究した結果、従来技術により得ら
れる筋状の微細孔を有する繊維構造とは異なった繊維構
造とすることにより、上記課題すべてが解決できること
を見いだし、本発明に達したものであり、本発明は、ポ
リアミド繊維を構成する単繊維が、おおよそその繊維軸
方向に並行に配列したフィブリルの緊密な集合体で構成
されることを特徴とするポリアミド繊維、および、ポリ
アミド70〜50重量%と、ポリエチレンテレフタレー
トにポリエチレングリコールを10〜30重量%共重合
したポリエステル30〜50重量%とのブレンドポリマ
ーを溶融紡糸して得た繊維をアルカリ減量処理して、共
重合ポリエステルを溶出除去することを特徴とするポリ
アミド繊維の製造方法、である。
Means for Solving the Problems As a result of intensive research for solving the above problems, the present inventors have found that a fiber structure different from the fiber structure having streak-shaped fine pores obtained by the prior art is used. The present invention has been found to be able to solve all the above-mentioned problems, and the present invention has been achieved. The present invention comprises monofilaments constituting polyamide fibers, which are composed of a tight aggregate of fibrils arranged substantially parallel to the fiber axis direction. Obtained by melt spinning a polyamide fiber, and a blend polymer of 70 to 50% by weight of polyamide and 30 to 50% by weight of polyester obtained by copolymerizing polyethylene terephthalate with 10 to 30% by weight of polyethylene glycol. Production of polyamide fiber, characterized in that the copolyester is eluted and removed by subjecting the treated fiber to alkali reduction treatment Law, it is.

【0006】本発明で用いるポリアミドとしては、ナイ
ロン6、ナイロン66、ナイロン610、ナイロン4
6、ナイロン12等の脂肪族ポリアミドが好ましい。ま
た、これらポリアミドはテレフタル酸、イソフタル酸等
の芳香族成分を共重合させたものであってもよいが、ナ
イロン6、ナイロン66であることが好ましい。なお、
上記ポリアミドには、必要に応じて任意の添加剤、例え
ば帯電防止剤、着色防止剤、難燃剤、艶消剤、着色剤等
が含まれていてもよい。
Polyamides used in the present invention include nylon 6, nylon 66, nylon 610, nylon 4
Aliphatic polyamides such as 6 and nylon 12 are preferred. Further, these polyamides may be those obtained by copolymerizing an aromatic component such as terephthalic acid and isophthalic acid, but nylon 6 and nylon 66 are preferable. In addition,
If necessary, the polyamide may contain any additive such as an antistatic agent, an anti-coloring agent, a flame retardant, a matting agent, and a coloring agent.

【0007】一方、本発明において用いる共重合ポリエ
ステルは、従来の公知技術でよく用いられているポリエ
チレンテレフタレートよりもポリアミドとの相溶性が良
好であることが必要であり、ポリアミドと微細に混合で
きることが必要である。そのためには、テレフタル酸を
主たる酸成分とし、エチレングリコールの他にポリエチ
レングリコールを主たるグリコール成分とすることが望
ましい。この場合、重合する際のポリエチレングリコー
ルの添加重量は、10〜30重量%とすることが好まし
い。ポリエチレングリコールの重量が10重量%未満で
あると微細に混合することが困難になり、また30重量
%より多いと共重合ポリエステルの耐熱性が不良とな
り、紡糸性および延伸性が低下し、糸切れが頻発する。
On the other hand, the copolyester used in the present invention needs to have better compatibility with polyamide than polyethylene terephthalate, which is often used in the conventional known techniques, and can be finely mixed with polyamide. is necessary. For that purpose, it is desirable to use terephthalic acid as a main acid component and polyethylene glycol as a main glycol component in addition to ethylene glycol. In this case, the added weight of polyethylene glycol at the time of polymerization is preferably 10 to 30% by weight. If the weight of polyethylene glycol is less than 10% by weight, it becomes difficult to finely mix it, and if it exceeds 30% by weight, the heat resistance of the copolyester becomes poor, and the spinnability and drawability deteriorate, resulting in yarn breakage. Frequently occurs.

【0008】有機スルホン酸金属塩含有ポリエステルは
用いない方が本発明の課題をより良く解決でき、もし用
いる場合には、5重量%以下に制限すべきである。本発
明の構成要件である共重合ポリエステルを用いた場合は
微細なフィブリルを形成させることができるが、これ以
外の共重合ポリエステルやポリエチレンテレフタレート
を用いた場合には、例えば特開平2−175965号公
報記載の図面に示されるような筋状孔を形成してしま
い、本発明と異なった繊維表面構造となるため、ポリア
ミド系繊維特有のぬめり感を有さず、軽量で、また吸水
性能、保水性能、放水性能に優れたポリアミド繊維を得
ることはできない。
The problem of the present invention can be better solved by not using the organic sulfonic acid metal salt-containing polyester, and if it is used, it should be limited to 5% by weight or less. Fine fibrils can be formed when the copolyester which is a constituent of the present invention is used, but when other copolyester or polyethylene terephthalate is used, for example, JP-A-2-175965. Forming streak-like holes as shown in the drawings described, because it has a different fiber surface structure from the present invention, does not have the slimy feeling peculiar to polyamide fibers, is lightweight, and also has water absorption performance and water retention performance. However, it is not possible to obtain polyamide fibers having excellent water discharge performance.

【0009】ポリアミドと共重合ポリエステルとの望ま
しい混合比率は、それぞれのポリマーの重合度や紡糸温
度等で若干変化するが、ポリアミド70〜50重量%、
共重合ポリエステル30〜50重量%にすることが好ま
しい。ポリアミドの混合比率が70重量%を越えると微
細なフィブリルを形成させることが困難になり、繊維表
面の変化は少なく、ポリエチレンテレフタレートとのブ
レンド繊維で知られているようにパール光沢を示すだけ
である。またポリアミドの混合比率が50重量%を下回
ると、生成したフィブリルが減量処理液中に分散してし
まい、繊維形態を保持し得なくなる。
The desirable mixing ratio of polyamide and copolyester varies depending on the degree of polymerization of each polymer and the spinning temperature, but is 70 to 50% by weight of polyamide.
Copolymerized polyester is preferably 30 to 50% by weight. When the mixing ratio of polyamide exceeds 70% by weight, it becomes difficult to form fine fibrils, the change of the fiber surface is small, and only pearl luster is exhibited as is known in the blended fiber with polyethylene terephthalate. . On the other hand, if the mixing ratio of the polyamide is less than 50% by weight, the produced fibrils will be dispersed in the weight reduction treatment liquid, and the fiber form will not be retained.

【0010】本発明の繊維を紡糸するにあたって、ポリ
アミドポリマーと共重合ポリエステルポリマーとは、予
めチップブレンドして用いればよい。また、紡糸に用い
る紡糸パックおよび紡糸口金は、常用のものを用いれば
よい。紡糸および延伸工程は連続しても、また一度パッ
ケージに巻取ったのち延伸してもよい。次いで、必要な
らば仮撚加工をしてのち、編物、織物などの組織にし、
アルカリ溶液で浸漬処理することにより、繊維から共重
合ポリエステルを容易に除去することができる。
When the fiber of the present invention is spun, the polyamide polymer and the copolyester polymer may be used as a chip blend in advance. The spinning pack and spinneret used for spinning may be conventional ones. The spinning and stretching steps may be continuous, or may be once wound into a package and then stretched. Then, if necessary, false twisting is performed, and then a structure such as a knitted fabric or a woven fabric is formed.
The copolyester can be easily removed from the fibers by the immersion treatment with an alkaline solution.

【0011】ここで使用するアルカリ溶液は、水酸化ナ
トリウム、水酸化カリウム、水酸化リチウム、炭酸ナト
リウム、炭酸カリウム、テトラメチルアンモニウムハイ
ドロサルファイト、およびこれらの混合物等の水溶液が
好ましいが、水酸化ナトリウム、水酸化カリウムが特に
好ましい。減量促進剤を用いることも好ましい。アルカ
リ溶液のアルカリ化合物の濃度は、アルカリ化合物の種
類、処理条件などによっても異なるが、通常は0.01
〜40重量%の範囲であり、その中でも0.1〜30重
量%の範囲が好ましい。
The alkaline solution used here is preferably an aqueous solution of sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium carbonate, potassium carbonate, tetramethylammonium hydrosulfite, or a mixture thereof. , Potassium hydroxide is particularly preferable. It is also preferable to use a weight loss promoter. The concentration of the alkaline compound in the alkaline solution varies depending on the type of the alkaline compound and the treatment conditions, but is usually 0.01.
The range is from -40% by weight, and the range is preferably from 0.1 to 30% by weight.

【0012】処理温度は通常室温〜100℃の範囲であ
り、処理時間は通常1分〜4時間の範囲が好ましく、1
分〜60分である方がより好ましい。このアルカリ溶液
の処理によって溶出除去する共重合ポリエステルの量
は、共重合ポリエステル含有量の少なくとも50重量%
であることが好ましい。この場合、90重量%以上を除
去することがより好ましい。
The treatment temperature is usually from room temperature to 100 ° C., and the treatment time is usually from 1 minute to 4 hours, preferably 1
Minutes to 60 minutes is more preferable. The amount of the copolyester to be eluted and removed by the treatment with the alkaline solution is at least 50% by weight of the content of the copolyester.
Is preferred. In this case, it is more preferable to remove 90% by weight or more.

【0013】このようにして得られたポリアミド繊維
は、第1〜2図(いずれも電子顕微鏡写真)に示すよう
に、ポリアミド繊維を構成する単繊維は、おおよそその
繊維軸方向に並行に配列した数μm以下のフィブリルの
緊密な集合体で構成される。アルカリ減量処理前後の単
繊維の外径変化は、誤差の範囲内でほとんどない。この
ような構造は従来知られていない。本発明の構造を有す
る繊維とすることにより初めて、ポリアミド系繊維特有
のぬめり感を有さず、軽量で、また吸水性能、保水性
能、放水性能に優れたポリアミド繊維を得ることができ
る。
As shown in FIGS. 1 and 2 (all electron micrographs) of the polyamide fiber thus obtained, the single fibers constituting the polyamide fiber are arranged approximately parallel to the fiber axis direction. It is composed of tightly packed aggregates of fibrils of a few μm or less. The change in outer diameter of the single fiber before and after the alkali weight reduction treatment is almost within the error range. Such a structure has not hitherto been known. The use of the fiber having the structure of the present invention makes it possible to obtain a polyamide fiber that does not have a slimy feeling peculiar to polyamide-based fibers, is lightweight, and is excellent in water absorption performance, water retention performance, and water discharge performance.

【0014】[0014]

【実施例】以下に実施例を記載して、本発明をさらに具
体的に説明する。ここに、 バイレック法吸水高さ:試料に0.1g/dの荷重をか
け、その一部を20℃の水中に10分間浸漬したのちに
吸い上げられた水柱の高さ 水分率:絶乾試料重量に対する吸水量の百分率 1G保水率:試料を水中に20分間浸漬したのち、水中
より取り出す。その一端をクリップで把持したのち5分
間懸下したあとの布帛の水分率。 154G保水率:840rpmの家庭用洗濯機の脱水機
(重力加速度の154倍の加速度に相当)で30秒間脱
水後の試料の水分率 1782G保水率:3500rpmのセントル型遠心脱
水機(重力加速度の1782倍に相当)で、回転が安定
してから5分間脱水後の試料の水分率 放水速度:3500rpmのセントル型遠心脱水機(重
力加速度の1782倍に相当)で、回転が安定してから
5分間脱水後の布帛を20℃、65RHの室内に10分
間放置乾燥した場合の10分間の平均の水分率減少率 である。
EXAMPLES The present invention will be described more concretely with reference to the following examples. Water absorption height by the Bayrec method: A load of 0.1 g / d was applied to the sample, and a part of the sample was immersed in water at 20 ° C for 10 minutes, and then the height of the water column sucked up Moisture content: Absolute dry sample weight Percentage of water absorption relative to 1 G water retention rate: After the sample is immersed in water for 20 minutes, it is taken out from the water. Moisture content of the fabric after gripping one end with a clip and hanging it for 5 minutes. 154G water retention rate: 840 rpm household washing machine dehydrator (corresponding to 154 times the acceleration of gravity) for 30 seconds after dehydration of the sample 1782 G water retention rate: 3500 rpm Centr type centrifugal dehydrator (gravitational acceleration of 1782) Moisture content of the sample after dehydration for 5 minutes after the rotation stabilizes. Centrifuge centrifugal dehydrator with a water discharge rate of 3500 rpm (equivalent to 1782 times the acceleration of gravity) for 5 minutes after the rotation stabilizes. It is the average reduction rate of water content in 10 minutes when the dehydrated fabric is left to dry in a room at 20 ° C. and 65 RH for 10 minutes.

【0015】[0015]

【実施例1】280℃での溶融粘度が400ポイズのナ
イロン66と、ジメチルテレフタレート51部、分子量
6000のポリエチレングリコール26部、エチレング
リコール23部より重合した280℃での溶融粘度が4
00ポイズの共重合ポリエステルとを用い、ナイロン6
6と共重合ポリエステルとの混合比を重量で60対40
としてチップブレンド紡糸したのち延伸し、293デニ
ール/48フィラメントの繊維を得た。
EXAMPLE 1 Nylon 66 having a melt viscosity of 400 poise at 280 ° C., 51 parts of dimethyl terephthalate, 26 parts of polyethylene glycol having a molecular weight of 6000, and 23 parts of ethylene glycol were polymerized to obtain a melt viscosity of 4 at 280 ° C.
Nylon 6 with 00 poise of copolyester
The mixing ratio of 6 and the copolyester is 60:40 by weight.
As a chip blend, the fiber was spun and then stretched to obtain a fiber of 293 denier / 48 filament.

【0016】この繊維を一口編地とし、5重量%の水酸
化ナトリウム水溶液を用い、90℃で10分間浸漬処理
し、共重合ポリエステルをほぼ完全に溶出除去した。見
かけの減量率は39重量%であった。この編地の表面を
走査型電子顕微鏡で2000倍に拡大して観察したとこ
ろ、単繊維の側面は2μm以下の微細フィブリルが繊維
軸方向に並行に配列したフィブリルの緊密な集合構造を
していた(図1)。ナイフで切断した単繊維の横断面
は、単繊維の内部までフィブリルの緊密な集合構造であ
ることを示していた(図2)。編地はポリアミド系繊維
特有のぬめり感を有さず、軽量で、ドライタッチ風合で
あった。
This fiber was used as a one-piece knitted fabric and immersed in a 5% by weight sodium hydroxide aqueous solution at 90 ° C. for 10 minutes to elute and remove the copolymerized polyester almost completely. The apparent weight loss rate was 39% by weight. When the surface of this knitted fabric was observed with a scanning electron microscope at a magnification of 2000 times, the side face of the single fiber had a close aggregate structure of fibrils in which fine fibrils of 2 μm or less were arranged in parallel in the fiber axis direction. (Figure 1). The cross section of the monofilament cut with a knife showed a tightly assembled structure of fibrils inside the monofilament (Fig. 2). The knitted fabric did not have the slimy feeling peculiar to polyamide-based fibers, was lightweight, and had a dry-touch feel.

【0017】ナイフで切断した単繊維の直径を測定した
ところ、アルカリ減量処理前は28.3μm、アルカリ
減量処理後は28.6μmであり、誤差範囲内で差はな
かった。ナイロン66の比重を1.14とすると、アル
カリ減量処理後の本実施例の繊維の見掛の比重は0.7
0であった。この編地を40℃の温水に浸漬したとこ
ろ、気泡を発しながら水面上に浮上し、やがて下に沈ん
だ。したがって、フィブリル感の空隙はある程度連続し
ているものと推定された。
When the diameter of the monofilament cut with a knife was measured, it was 28.3 μm before the alkali weight reduction treatment and 28.6 μm after the alkali weight reduction treatment, and there was no difference within the error range. Assuming that the specific gravity of nylon 66 is 1.14, the apparent specific gravity of the fiber of this example after the alkali reduction treatment is 0.7.
It was 0. When this knitted fabric was immersed in warm water of 40 ° C., it floated above the water surface while generating bubbles, and eventually sank below. Therefore, it was estimated that the fibril-like voids were continuous to some extent.

【0018】また、編地よりほどいた繊維のバイレック
法吸水高さは74mm、編地の1G保水率は240%、
154G保水率は135%、1782G保水率は68
%、放水速度は1.5%/分といづれも大であった。す
なわち高吸水性、高保水性、高速乾性であった。ちなみ
に、綿繊維のバイレック法吸水高さは43mm、編地の
1G保水率は189%、154G保水率は109%、1
782G保水率は44%、放水速度は1.1%/分であ
った。
Further, the water absorption height of the fibers unwound from the knitted fabric is 74 mm, the 1G water retention rate of the knitted fabric is 240%,
154G water retention rate is 135%, 1782G water retention rate is 68%
%, And the water discharge rate was 1.5% / min, which were both large. That is, it had a high water absorption property, a high water retention property and a high speed drying property. By the way, the water absorption height of the Bayrek method of cotton fiber is 43 mm, the 1G water retention rate of the knitted fabric is 189%, the 154G water retention rate is 109%, 1
The 782G water retention rate was 44%, and the water discharge rate was 1.1% / min.

【0019】[0019]

【実施例2】280℃での溶融粘度が400ポイズのナ
イロン66と、ジメチルテレフタレート59部、分子量
6000のポリエチレングリコール15部、エチレング
リコール26部より重合した280℃での溶融粘度が4
00ポイズの共重合ポリエステルとを用い、ナイロン6
6と共重合ポリエステルとの混合比を重量で65対35
としてチップブレンド紡糸したのち延伸し、290デニ
ール/48フィラメントの繊維を得た。
Example 2 Nylon 66 having a melt viscosity of 400 poise at 280 ° C., 59 parts of dimethyl terephthalate, 15 parts of polyethylene glycol having a molecular weight of 6000 and 26 parts of ethylene glycol were polymerized to obtain a melt viscosity of 4 at 280 ° C.
Nylon 6 with 00 poise of copolyester
The mixing ratio of 6 and the copolyester is 65:35 by weight.
As a chip blend, it was spun and then stretched to obtain 290 denier / 48 filament fibers.

【0020】この繊維を一口編地とし、5重量%の水酸
化ナトリウム水溶液を用い、90℃で30分間浸漬処理
し、共重合ポリエステルをほぼ完全に溶出除去した。見
かけの減量率は33重量%であった。この編地の表面を
走査型電子顕微鏡で2000倍に拡大して観察したとこ
ろ、単繊維の側面は2μm以下の微細フィブリルが繊維
軸方向に並行に配列したフィブリルの緊密な集合構造を
していた。ナイフで切断した単繊維の横断面は、単繊維
の内部までフィブリルの緊密な集合構造であることを示
していた。編地はポリアミド系繊維特有のぬめり感を有
さず、軽量で、ドライタッチ風合であった。
This fiber was used as a one-piece knitted fabric and was immersed in a 5% by weight aqueous solution of sodium hydroxide at 90 ° C. for 30 minutes to elute and remove the copolymerized polyester almost completely. The apparent weight loss rate was 33% by weight. When the surface of this knitted fabric was observed with a scanning electron microscope at a magnification of 2000 times, the side face of the single fiber had a close aggregate structure of fibrils in which fine fibrils of 2 μm or less were arranged in parallel in the fiber axis direction. . The cross section of the monofilament cut with a knife showed a tightly assembled structure of fibrils inside the monofilament. The knitted fabric did not have the slimy feeling peculiar to polyamide-based fibers, was lightweight, and had a dry-touch feel.

【0021】編地よりほどいた繊維のバイレック法吸水
高さは72mm、編地の1G保水率は232%、154
G保水率は131%、1782G保水率は62%、放水
速度は1.6%/分といづれも大であった。すなわち高
吸水性、高保水性、高速乾性であった。
The water absorption height of the fibers unwound from the knitted fabric was 72 mm, and the 1G water retention rate of the knitted fabric was 232%, 154.
The G water retention rate was 131%, the 1782G water retention rate was 62%, and the water discharge rate was 1.6% / min. That is, it had a high water absorption property, a high water retention property and a high speed drying property.

【0022】[0022]

【比較例1】鞘成分として280℃での溶融粘度が40
0ポイズのポリエチレンテレフタレートを用いた以外は
実施例1と同様にして紡糸、延伸したが、糸切れが頻発
してサンプリング不可能であった。
Comparative Example 1 As a sheath component, the melt viscosity at 280 ° C. is 40.
Spinning and drawing were performed in the same manner as in Example 1 except that 0 poise of polyethylene terephthalate was used, but yarn breakage occurred frequently and sampling was impossible.

【0023】[0023]

【比較例2】280℃での溶融粘度が400ポイズのナ
イロン66をL型の吐出孔を有する紡糸口金を用いて溶
融紡糸、延伸し、60d/48fの繊維を得た。この繊
維を一口編としてから、ほどいた繊維のバイレック法吸
水高さは29mmと小であり吸水性能は綿より劣るもの
であった。また編地の1G保水率は304%、154G
保水率は209%で綿より優れるものであったが、17
82G保水率は14%で綿より劣るものであった。
Comparative Example 2 Nylon 66 having a melt viscosity of 400 poise at 280 ° C. was melt-spun and drawn using a spinneret having an L-shaped discharge hole to obtain a fiber of 60d / 48f. After the fiber was formed into a single knit, the unwound fiber had a small water absorption height of 29 mm, which was inferior to that of cotton. The 1G water retention rate of the knitted fabric is 304%, 154G
The water retention rate was 209%, which was superior to that of cotton.
The water retention rate of 82G was 14%, which was inferior to cotton.

【0024】[0024]

【発明の効果】以上に説明した通り、本発明によれば、
ポリアミド系繊維特有のぬめり感を有さず、軽量で、吸
水性能、保水性能、放水性能に優れた新規なポリアミド
繊維を得ることができる。
As described above, according to the present invention,
It is possible to obtain a novel polyamide fiber that does not have a slimy feeling peculiar to polyamide-based fibers, is lightweight, and has excellent water absorption performance, water retention performance, and water discharge performance.

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

【図1】本発明の吸水性ポリアミド繊維の側面の表面状
態の一例を示す電子顕微鏡写真(x2,000)であ
る。
FIG. 1 is an electron micrograph (x2,000) showing an example of a surface state of a side surface of a water-absorbent polyamide fiber of the present invention.

【図2】本発明の吸水性ポリアミド繊維の横断面の表面
状態の一例を示す電子顕微鏡写真(x2,000)であ
る。
FIG. 2 is an electron micrograph (x2,000) showing an example of a surface state of a cross section of the water-absorbent polyamide fiber of the present invention.

─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成5年12月27日[Submission date] December 27, 1993

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】図面[Document name to be corrected] Drawing

【補正対象項目名】図1[Name of item to be corrected] Figure 1

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【図1】 [Figure 1]

【手続補正2】[Procedure Amendment 2]

【補正対象書類名】図面[Document name to be corrected] Drawing

【補正対象項目名】図2[Name of item to be corrected] Figure 2

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【図2】 [Fig. 2]

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 D06M 101:34 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location D06M 101: 34

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 ポリアミド繊維を構成する単繊維が、お
およそその繊維軸方向に並行に配列したフィブリルの緊
密な集合体で構成されることを特徴とするポリアミド繊
維。
1. A polyamide fiber characterized in that the single fiber constituting the polyamide fiber is constituted by a tight aggregate of fibrils arranged substantially parallel to the fiber axis direction.
【請求項2】 ポリアミド70〜50重量%と、ポリエ
チレンテレフタレートにポリエチレングリコールを10
〜30重量%共重合したポリエステル30〜50重量%
とのブレンドポリマーを溶融紡糸して得た繊維をアルカ
リ減量処理して、共重合ポリエステルを溶出除去するこ
とを特徴とするポリアミド繊維の製造方法。
2. Polyamide 70 to 50% by weight, polyethylene terephthalate and polyethylene glycol 10
-30% by weight Copolymerized polyester 30-50% by weight
A method for producing a polyamide fiber, which comprises subjecting a fiber obtained by melt-spinning a blended polymer of (1) to (3) to alkali reduction treatment to elute and remove the copolyester.
JP32423593A 1993-12-22 1993-12-22 Water-absorbing polyamide fiber and its production Pending JPH07189119A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32423593A JPH07189119A (en) 1993-12-22 1993-12-22 Water-absorbing polyamide fiber and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32423593A JPH07189119A (en) 1993-12-22 1993-12-22 Water-absorbing polyamide fiber and its production

Publications (1)

Publication Number Publication Date
JPH07189119A true JPH07189119A (en) 1995-07-25

Family

ID=18163552

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32423593A Pending JPH07189119A (en) 1993-12-22 1993-12-22 Water-absorbing polyamide fiber and its production

Country Status (1)

Country Link
JP (1) JPH07189119A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006525442A (en) * 2003-04-30 2006-11-09 サーントル ナシオナル ドゥ ラ ルシェルシェ シャーンティフィク(セーエンヌエールエス) Method for producing fiber having high content of colloidal particles and composite fiber obtained therefrom

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006525442A (en) * 2003-04-30 2006-11-09 サーントル ナシオナル ドゥ ラ ルシェルシェ シャーンティフィク(セーエンヌエールエス) Method for producing fiber having high content of colloidal particles and composite fiber obtained therefrom

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