JP2844293B2 - Processing method of woven and knitted material containing acetate fiber - Google Patents

Processing method of woven and knitted material containing acetate fiber

Info

Publication number
JP2844293B2
JP2844293B2 JP5148237A JP14823793A JP2844293B2 JP 2844293 B2 JP2844293 B2 JP 2844293B2 JP 5148237 A JP5148237 A JP 5148237A JP 14823793 A JP14823793 A JP 14823793A JP 2844293 B2 JP2844293 B2 JP 2844293B2
Authority
JP
Japan
Prior art keywords
woven
knitted fabric
acetate
fiber
acetate 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.)
Expired - Fee Related
Application number
JP5148237A
Other languages
Japanese (ja)
Other versions
JPH06341066A (en
Inventor
孝 野中
睦生 山崎
博美 保永
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.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon 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 Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP5148237A priority Critical patent/JP2844293B2/en
Publication of JPH06341066A publication Critical patent/JPH06341066A/en
Application granted granted Critical
Publication of JP2844293B2 publication Critical patent/JP2844293B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

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、アセテート繊維含有織
編物の加工方法に係わり、さらに詳しくはアセテート繊
維含有織編物の構成糸条に捲縮を付与し柔軟で良好な風
合いを与えるアセテート繊維含有織編物の加工方法に関
する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for processing an woven or knitted fabric containing acetate fibers, and more particularly, to a method for imparting a crimp to the constituent yarns of the woven or knitted fabric containing acetate fibers to give a soft and good texture. The present invention relates to a method for processing a woven or knitted fabric.

【0002】[0002]

【従来の技術】近年、衣料用繊維分野においては、消費
者ニーズの多様化、高級化の流れにより、各種の天然、
化学繊維で様々な改質や改良が行われている。そして、
アセテート繊維についても、繊維断面、表面、糸形態等
を変化させ、光沢感や風合いの改良がなされてきてい
る。特にアセテート繊維糸条において捲縮を形成する手
法としては、高速度の仮撚スピンドル及びヒーターによ
って連続的に加撚、熱セット、解撚を行う方法が主とし
て採用されている。しかしながら、仮撚による方法で
は、繊維強度等が限定要因となり、超微細な捲縮を形成
させることが困難である。また、仮撚による方法以外の
捲縮を発現させる方法として、特公昭47−37205
号公報に予備延伸後、膨潤剤水溶液に傾斜角をもたせて
浸漬してランダム捲縮を生じさせる方法が開示されてい
るが、この方法でも大きな捲縮は得られるが、非常に微
細な捲縮を得ることは不可能である。
2. Description of the Related Art In recent years, in the field of textiles for clothing, various natural,
Various modifications and improvements have been made in chemical fibers. And
Acetate fibers have also been improved in glossiness and feel by changing the fiber cross section, surface, yarn form, and the like. In particular, as a method of forming crimps in an acetate fiber yarn, a method of continuously twisting, heat setting, and untwisting using a high-speed false twist spindle and a heater is mainly employed. However, in the false twisting method, the fiber strength and the like are a limiting factor, and it is difficult to form an ultrafine crimp. As a method of expressing crimps other than the method of false twisting, JP-B-47-37205 is used.
In Japanese Patent Application Laid-Open Publication No. H10-157, a method is disclosed in which after pre-stretching, a random crimp is generated by immersing the swelling agent in an aqueous solution at an inclined angle to generate a random crimp, but a large crimp can be obtained by this method, but a very fine crimp is obtained. It is impossible to get.

【0003】[0003]

【発明が解決しようとする課題】本発明は、アセテート
繊維を織編物の構成糸条の一つとし、織編物の状態でそ
の構成糸条に微細な捲縮を付与する方法を提供すもの
で、本発明の目的は、織編物を構成するアセテート繊維
糸条に超微細な捲縮を形成し、滑らかな光沢と絹様の手
触りの風合いを有するアセテート繊維含有織編物を得る
ことにある。
SUMMARY OF THE INVENTION The present invention provides a method for forming acetate fibers into one of the constituent yarns of a woven or knitted fabric and imparting a fine crimp to the constituent yarns in a woven or knitted state. An object of the present invention is to provide an acetate fiber-containing woven or knitted fabric having an ultrafine crimp formed on an acetate fiber yarn constituting a woven or knitted fabric and having a smooth gloss and a silky texture.

【0004】[0004]

【課題を解決するための手段】本発明は、アセテート繊
維糸条と他の繊維糸条とから構成した織編物をアルカリ
化合物にて処理して含有するアセテート繊維の表面を鹸
化した後、セルロースの分解酵素若しくは抜蝕剤にて処
理して該鹸化部の一部または全部を分解除去し、次いで
96℃以上の温度の湿熱下で加熱処理することを特徴と
する新規なアセテート繊維含有織編物の加工方法にあ
る。
SUMMARY OF THE INVENTION The present invention relates to a method for treating cellulose acetate fibers comprising treating a woven or knitted fabric comprising an acetate fiber yarn and another fiber yarn with an alkali compound to saponify the surface of the acetate fiber. A novel acetate fiber-containing woven or knitted fabric characterized by decomposing and removing part or all of the saponified portion by treating with a decomposing enzyme or a disinfectant, and then performing heat treatment under a moist heat at a temperature of 96 ° C. or more. In the processing method.

【0005】本発明における織編物とは、酢化度が45
〜59.5%のジアセテート繊維および酢化度が59.
5%を超えるトリアセテート繊維から選ばれるアセテー
ト繊維糸条と、他の繊維糸条とから構成してなる織編物
をいい、他の繊維としては、ポリエステル繊維、ポリア
ミド繊維、アクリル繊維等の合成繊維が好ましく用いら
れる。特に、本発明においては、経糸または緯糸の一方
をアセテート繊維糸条で構成し、他方を他の繊維糸条で
構成した織物を用いることが好ましい。また、織編物に
おけるアセテート繊維糸条は、アセテート繊維のみの糸
条でも、他の繊維を含む糸条であってもよい。織編物で
のアセテート繊維の比率は、織編物強度とアセテート繊
維の捲縮付与効果等を考慮し任意に設定しうる。
The woven or knitted fabric of the present invention has a degree of acetylation of 45.
〜59.5% diacetate fiber and a degree of acetylation of 59.5%.
A woven or knitted fabric composed of acetate fiber yarns selected from triacetate fibers exceeding 5% and other fiber yarns. Other fibers include synthetic fibers such as polyester fibers, polyamide fibers, and acrylic fibers. It is preferably used. In particular, in the present invention, it is preferable to use a woven fabric in which one of the warp and the weft is composed of an acetate fiber thread and the other is composed of another fiber thread. Further, the acetate fiber yarn in the woven or knitted fabric may be a yarn containing only acetate fibers or a yarn containing other fibers. The ratio of the acetate fibers in the woven or knitted fabric can be arbitrarily set in consideration of the strength of the woven or knitted fabric, the effect of imparting crimp of the acetate fibers, and the like.

【0006】本発明においては、かかるアセテート繊維
織編物をアルカリ化合物にて処理する必要がある。この
アルカリ処理に用いられるアルカリ化合物としては、苛
性ソーダ等のアルカリ金属水酸化物、水酸化カルシウム
等のアルカリ土類金属水酸化物、炭酸ソーダ等のアルカ
リ金属塩が挙げられる。
In the present invention, it is necessary to treat such an acetate fiber woven or knitted fabric with an alkali compound. Examples of the alkali compound used in the alkali treatment include alkali metal hydroxides such as caustic soda, alkaline earth metal hydroxides such as calcium hydroxide, and alkali metal salts such as sodium carbonate.

【0007】アルカリ処理は、繊維の種類、捲縮付与の
程度即ち求める風合いの程度等により異なるが、織編物
をアルカリ化合物1〜40wt%の水溶液に浸漬し、室
温〜130℃の加温下で5〜120分処理し、織編物に
含まれる少なくともアセテート繊維の繊維表面を鹸化す
る。また、このアルカリ処理の際、公知の減量促進剤を
併用することも可能である。
The alkali treatment varies depending on the type of fiber and the degree of crimping, that is, the degree of texture required. However, the woven or knitted fabric is immersed in an aqueous solution of 1 to 40% by weight of an alkali compound, and heated at room temperature to 130 ° C. The treatment is carried out for 5 to 120 minutes to saponify at least the surface of the acetate fiber contained in the woven or knitted fabric. In addition, at the time of this alkali treatment, a known weight loss accelerator can be used in combination.

【0008】次いで、本発明においては、アルカリ処理
された織編物を、セルロース分解酵素処理若しくはセル
ロース抜蝕剤処理することにより、織編物中のアセテー
ト繊維表面の鹸化により生成するセルロースを分解除去
する。
In the present invention, the alkali-treated woven or knitted fabric is treated with a cellulose-decomposing enzyme or a cellulose disinfectant to decompose and remove the cellulose produced by saponifying the surface of the acetate fiber in the woven or knitted fabric.

【0009】酵素処理に用いられるセルロース分解酵素
としては、セルロースを加水分解するセルラーゼであ
り、糸状菌のトリコデルマ属、アスペルギルス属等の起
源のものがあり、オノズカR−10(ヤクルト社製)、
メイセラーゼ(明治製菓社製)、セルクラスト1.5L
(ノボ社製)等の商品名で容易に入手しうる。
The cellulolytic enzyme used in the enzymatic treatment is a cellulase that hydrolyzes cellulose, and is derived from fungi such as Trichoderma and Aspergillus. Onozuka R-10 (manufactured by Yakult),
Meisserase (Meiji Seika Co., Ltd.), Cell Crust 1.5L
It can be easily obtained under a trade name such as (manufactured by Novo).

【0010】酵素処理は、アルカリ処理でのアセテート
繊維の鹸化の程度、求める風合いの程度等により異なる
が、アルカリ処理された織編物を酢酸等によるpH3.
5〜7.0のセルロース分解酵素1〜50g/lの水溶
液に浸漬し、20〜65℃で2〜240分処理する。こ
の酵素処理の程度により織編物中のアセテート繊維の鹸
化部の一部または全部が分解除去され減量化が行われ
る。織編物に付着残留した酵素は、80℃以上の熱水中
に浸漬する等加熱することにより容易に失活させること
ができる。
The enzymatic treatment varies depending on the degree of saponification of the acetate fiber in the alkaline treatment, the degree of the desired texture, and the like.
It is immersed in an aqueous solution of 1 to 50 g / l of cellulolytic enzyme of 5 to 7.0 and treated at 20 to 65 ° C for 2 to 240 minutes. Depending on the degree of this enzyme treatment, part or all of the saponified portion of the acetate fiber in the woven or knitted material is decomposed and removed, thereby reducing the weight. The enzyme remaining on the woven or knitted fabric can be easily deactivated by heating, such as immersion in hot water of 80 ° C. or higher.

【0011】また、セルロース抜蝕剤処理する場合に
は、用いられる抜蝕剤としては、セルロースを炭化、加
水分解する酸類が好ましく、硫酸、塩酸等の無機酸、硫
酸水素ナトリウム、硫酸アルミニウム、硫酸第二鉄、硫
酸アンモニウム、硫酸亜鉛、硫酸第一錫等の硫酸塩、塩
化第一鉄、塩化第二鉄、塩化アルミニウム、塩化マグネ
シウム、塩化亜鉛、塩化コバルト、塩化第一銅、塩化第
二銅、塩化ニッケル、塩化第一錫、塩化第二錫等の塩化
物、塩素酸ナトリウム、塩素酸アルミニウム、塩素酸カ
リウム、亜塩素酸ナトリウム等の塩素酸塩類、硝酸クロ
ム、硝酸銅、硝酸亜鉛等の硝酸塩、蓚酸第一鉄、蓚酸第
二鉄、蓚酸第一錫等の蓚酸塩、酢酸亜鉛等の酢酸塩、燐
酸亜鉛等の燐酸塩、アルキルナフタレンスルホン酸等の
有機酸が挙げられる。
In the case of treating with a cellulose disinfectant, the disinfectant used is preferably an acid that carbonizes and hydrolyzes cellulose, inorganic acids such as sulfuric acid and hydrochloric acid, sodium hydrogen sulfate, aluminum sulfate, and sulfuric acid. Ferric, ammonium sulfate, zinc sulfate, sulfates such as stannous sulfate, ferrous chloride, ferric chloride, aluminum chloride, magnesium chloride, zinc chloride, cobalt chloride, cuprous chloride, cupric chloride, Chloride such as nickel chloride, stannous chloride and stannic chloride; chlorates such as sodium chlorate, aluminum chlorate, potassium chlorate, sodium chlorite; nitrates such as chromium nitrate, copper nitrate and zinc nitrate Oxalates such as ferrous oxalate, ferric oxalate, stannous oxalate, acetates such as zinc acetate, phosphates such as zinc phosphate, and organic acids such as alkylnaphthalenesulfonic acid.

【0012】抜蝕剤処理は、繊維の種類、抜蝕剤の種
類、捲縮付与の程度即ち求める風合いの程度により異な
るが、アルカリ処理された織編物を抜蝕剤0.5〜20
wt%の水溶液に浸漬し、或いはさらに加温する。この
抜蝕剤処理により織編物中のアセテート繊維の鹸化部の
一部または全部が分解除去される。
The disinfectant treatment depends on the type of fiber, the disinfectant, and the degree of crimping, that is, the degree of texture required.
It is immersed in a wt% aqueous solution or further heated. By this disinfectant treatment, part or all of the saponified portion of the acetate fiber in the woven or knitted material is decomposed and removed.

【0013】一般に抜蝕剤の酸類は、アセテート繊維も
侵蝕するが、セルロースが酸類の作用に極めて鋭敏なた
めに、抜蝕剤水溶液の濃度、温度のコントロールにより
容易に鹸化部のセルロースのみを分解除去しうる。
In general, the acids of the disinfectant also attack the acetate fibers. However, since cellulose is extremely sensitive to the action of the acids, only the cellulose in the saponified portion can be easily decomposed by controlling the concentration and temperature of the aqueous solution of the disinfectant. Can be removed.

【0014】さらに、本発明においては、セルロース分
解酵素処理若しくはセルロース抜蝕剤処理された織編物
を、96℃以上の温度の湿熱下で加熱処理する。加熱方
法としては、スチーム加熱、熱水中への浸漬等が用いら
れ、アセテート繊維糸条に捲縮を発現させるためには水
分を含む雰囲気下で加熱することが必須であり、乾熱下
では捲縮が発現しない。また、湿熱下であっても96℃
未満の温度では捲縮が発現しない。特に、超微細な捲縮
を発現させるには、99℃以上の熱水中に浸漬すること
が好ましく、処理時間は2分以上であることが好まし
い。
Further, in the present invention, the woven or knitted fabric which has been treated with the cellulose degrading enzyme or the cellulose disinfectant is subjected to a heat treatment at a temperature of 96 ° C. or more under moist heat. As a heating method, steam heating, immersion in hot water, or the like is used.In order to develop crimp on the acetate fiber yarn, it is essential to heat in an atmosphere containing moisture, and in dry heat No crimps appear. 96 ° C even under moist heat
At a temperature lower than the above, crimp does not appear. In particular, in order to develop ultra-fine crimps, it is preferable to immerse in hot water of 99 ° C. or more, and it is preferable that the treatment time is 2 minutes or more.

【0015】かかる加熱処理により、織編物を構成する
アセテート繊維糸条に非常に微細な捲縮が形成され、そ
の繊維軸方向に5000個/m以上のランダムな捲縮が
付与される。
By such heat treatment, very fine crimps are formed on the acetate fiber yarns constituting the woven or knitted fabric, and a random crimp of 5,000 / m or more is given in the fiber axis direction.

【0016】本発明の加工方法においては、アルカリ処
理と酵素処理若しくは抜蝕剤処理および湿熱加熱処理に
より、織編物の状態でその構成アセテート繊維糸条に超
微細な捲縮を形成させることができ、形成された超微細
な捲縮により新規な風合いを有する織編物を得ることが
できる。
In the processing method of the present invention, an ultra-fine crimp can be formed on the acetate fiber yarn in a woven or knitted state by an alkali treatment and an enzyme treatment or a disinfectant treatment and a wet heat treatment. A woven or knitted fabric having a new texture can be obtained by the formed ultrafine crimp.

【0017】[0017]

【実施例】以下、実施例により本発明を具体的に説明す
る。 (実施例1) 酢化度56.9%のジアセテート長繊維(ブライト75
d/21f)を経糸に、ポリエステル長繊維の仮撚加工
糸(セミダル75d/36f)を緯糸に用い、経密度2
00本/インチ、緯密度83本/インチの5枚朱子織物
に製織し、精練、乾燥した。この織物を液流染色機を用
いて、ジアセテート長繊維に対し9wt%の苛性ソーダ
水溶液に浸漬し80℃で60分処理した後、常温で清水
で洗浄しアルカリを除去し、風乾した。このアルカリ処
理によりジアセテート長繊維の減量率が9.5wt%で
ある織物を得た。
The present invention will be described below in detail with reference to examples. (Example 1) A diacetate long fiber having a degree of acetylation of 56.9% (Bright 75
d / 21f) as the warp, and polyester filament false twisted yarn (semi-dal 75d / 36f) as the weft.
The woven fabric was woven into five satin woven fabrics of 00 strands / inch and a weft density of 83 strands / inch, scoured and dried. This woven fabric was immersed in a 9 wt% aqueous solution of caustic soda with respect to the diacetate long fiber using a jet dyeing machine, treated at 80 ° C. for 60 minutes, washed with clear water at room temperature to remove alkali, and air-dried. By this alkali treatment, a woven fabric having a diacetate long fiber reduction rate of 9.5 wt% was obtained.

【0018】次いで、このアルカリ処理織物を、セルク
ラスト1.5L(ノボ社製)5g/l、バイオアシスト
MT(森六社製ノニオン系浸透剤)5g/lを含むpH
4.8、53℃、浴比1:100の水溶液に120分浸
漬、攪拌した後、水洗した。続いて、100℃の熱水中
にフリーな状態で10分浸漬した後、乾燥した。得られ
た織物は、そのジアセテート長繊維からなる経糸に繊維
軸方向に5800個/mの超微細な捲縮を有し、ふくら
みのある滑らかな光沢を有し、絹様の手触りを有するも
のであった。
Next, the alkali-treated fabric was treated with a pH value containing 5 g / l of 1.5 g of cell crust (manufactured by Novo) and 5 g / l of bioassist MT (nonionic penetrant manufactured by Moriroku).
It was immersed in an aqueous solution having a bath ratio of 4.8, 53 ° C. and a bath ratio of 1: 100 for 120 minutes, stirred, and then washed with water. Then, it was immersed in hot water of 100 ° C. for 10 minutes in a free state, and then dried. The obtained woven fabric has an ultrafine crimp of 5800 pcs / m in the fiber axis direction, a swelling smooth luster, and a silky feel to the warp composed of the diacetate filaments. Met.

【0019】(実施例2)実施例1で得られたアルカリ
処理織物を、硫酸水素ナトリウム・1水和物(硫酸とし
て34〜37%)を抜蝕剤として用い、その5wt%水
溶液に浸漬し、ニップして液量で90wt%含浸させた
後、130℃で10分間スチーミングして鹸化部のセル
ロースを分解し、水中で攪拌し分解物を脱落除去して水
洗後、乾燥した。次いで、100℃の熱水中にフリーの
状態で10分浸漬した後、乾燥した。得られた織物は、
そのジアセテート長繊維からなる経糸に繊維軸方向に6
200個/mの超微細な捲縮を有し、ふくらみのある滑
らかな光沢を有し、絹様の手触りを有するものであっ
た。
(Example 2) The alkali-treated fabric obtained in Example 1 was immersed in a 5 wt% aqueous solution thereof using sodium hydrogen sulfate monohydrate (34 to 37% as sulfuric acid) as a disinfectant. After the nip, the mixture was impregnated with 90% by weight of a liquid, steamed at 130 ° C. for 10 minutes to decompose the cellulose in the saponified portion, stirred in water to remove the decomposed product, washed with water, and dried. Next, it was immersed in hot water of 100 ° C. for 10 minutes in a free state, and then dried. The resulting fabric is
The warp composed of the diacetate filaments has a length of 6 in the fiber axis direction.
It had an ultrafine crimp of 200 pieces / m, had a swelling smooth luster, and had a silky feel.

【0020】[0020]

【発明の効果】本発明によれば、アセテート繊維と他の
繊維を複合化することによる機能性や意匠性或いは風合
いの改良と共に、織編物を構成するアセテート繊維糸条
に超微細な捲縮の形成により、ふくらみのある滑らかな
光沢を有し、絹様の手触りを有する織編物が得られ、し
かも、アセテート繊維の優れた発色性も併せ有する織編
物が得られる。
According to the present invention, the acetate fiber and the other fibers are combined to improve the functionality, the design, or the texture, and the acetate fiber yarn constituting the woven or knitted fabric is formed into a very fine crimp. By forming, a woven or knitted material having a swelling smooth luster and a silky feel can be obtained, and also a woven or knitted material having excellent coloring properties of acetate fibers can be obtained.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 保永 博美 愛知県名古屋市東区砂田橋四丁目1番60 号 三菱レイヨン株式会社商品開発研究 所内 (56)参考文献 特開 平2−216282(JP,A) 特開 平3−51376(JP,A) (58)調査した分野(Int.Cl.6,DB名) D06M 11/00 - 16/00──────────────────────────────────────────────────続 き Continuation of the front page (72) Inventor Hiromi Hosunaga 4-160 Sunadabashi, Higashi-ku, Nagoya-shi, Aichi Mitsubishi Rayon Co., Ltd. Product Development Laboratory (56) References JP-A-2-216282 (JP, A) JP-A-3-51376 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) D06M 11/00-16/00

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 アセテート繊維糸条と他の繊維糸条とか
ら構成した織編物をアルカリ化合物にて処理して含有す
るアセテート繊維の表面を鹸化した後、セルロースの分
解酵素若しくは抜蝕剤にて処理して該鹸化部の一部また
は全部を分解除去し、次いで96℃以上の温度の湿熱下
で加熱処理することを特徴とするアセテート繊維含有織
編物の加工方法。
A woven or knitted fabric composed of an acetate fiber yarn and another fiber yarn is treated with an alkali compound to saponify the surface of the contained acetate fiber and then treated with a cellulose decomposing enzyme or a disinfectant. A method for processing an acetate fiber-containing woven or knitted fabric, which comprises decomposing and removing part or all of the saponified portion, and then subjecting the saponified portion to heat treatment at a temperature of 96 ° C. or more under moist heat.
【請求項2】 加熱処理を99℃以上の温度の湿熱下で
行う請求項1記載のアセテート繊維含有織編物の加工方
法。
2. The method for processing a woven or knitted fabric containing acetate fibers according to claim 1, wherein the heat treatment is performed under moist heat at a temperature of 99 ° C. or higher.
【請求項3】 織編物として経糸または緯糸の一方をア
セテート繊維糸条で構成し、他方を他の繊維糸条で構成
した織物を用いる請求項1または請求項2記載のアセテ
ート繊維含有織編物の加工方法。
3. The acetate-fiber-containing woven or knitted fabric according to claim 1, wherein one of the warp and the weft is constituted by an acetate fiber yarn and the other is constituted by another fiber yarn. Processing method.
JP5148237A 1993-05-28 1993-05-28 Processing method of woven and knitted material containing acetate fiber Expired - Fee Related JP2844293B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5148237A JP2844293B2 (en) 1993-05-28 1993-05-28 Processing method of woven and knitted material containing acetate fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5148237A JP2844293B2 (en) 1993-05-28 1993-05-28 Processing method of woven and knitted material containing acetate fiber

Publications (2)

Publication Number Publication Date
JPH06341066A JPH06341066A (en) 1994-12-13
JP2844293B2 true JP2844293B2 (en) 1999-01-06

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Country Link
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100469011B1 (en) * 2002-06-21 2005-02-02 주식회사 유상실업 Burn out finishing of polyester fiber
KR100615668B1 (en) * 2005-05-11 2006-08-25 주식회사 유상실업 Burn-out finishing of polyamide
KR101398742B1 (en) * 2012-09-12 2014-05-27 한국섬유개발연구원 Process Of Producing Cellulose Diacetate/Nylon Composite Fabrics Having Exellent Stretch And Water―Washability

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02216282A (en) * 1988-10-27 1990-08-29 Kanebo Ltd Method for weight reduction processing of cellulosic fiber structure
JPH0351376A (en) * 1989-07-18 1991-03-05 Daido Maruta Senko Kk Enzymatic modification of cellulosic fiber

Also Published As

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