JPH083869A - Processing of yarn composed of cellulosic fiber - Google Patents

Processing of yarn composed of cellulosic fiber

Info

Publication number
JPH083869A
JPH083869A JP13453694A JP13453694A JPH083869A JP H083869 A JPH083869 A JP H083869A JP 13453694 A JP13453694 A JP 13453694A JP 13453694 A JP13453694 A JP 13453694A JP H083869 A JPH083869 A JP H083869A
Authority
JP
Japan
Prior art keywords
yarn
cellulosic fiber
solution
processing
dissolving
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.)
Granted
Application number
JP13453694A
Other languages
Japanese (ja)
Other versions
JP2604323B2 (en
Inventor
Katsuji Kasahara
勝次 笠原
Shinji Sakai
信治 酒井
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.)
DAITO KOSAN KK
NIIGATA PREF GOV
Niigata Prefecture
Original Assignee
DAITO KOSAN KK
NIIGATA PREF GOV
Niigata Prefecture
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 DAITO KOSAN KK, NIIGATA PREF GOV, Niigata Prefecture filed Critical DAITO KOSAN KK
Priority to JP6134536A priority Critical patent/JP2604323B2/en
Publication of JPH083869A publication Critical patent/JPH083869A/en
Application granted granted Critical
Publication of JP2604323B2 publication Critical patent/JP2604323B2/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)

Abstract

PURPOSE:To provide a process for the treatment of a yarn composed of cellulosic fiber and capable of dissolving and removing exclusively the fluffs in high workability simply by immersing the yarn in a liquid without necessitating time-consuming enzymatic treatment requiring delicate temperature control and the troublesome operations such as rubbing. CONSTITUTION:A yarn composed of cellulosic fibers is immersed in the form of yarn before weaving to a fabric in a dissolution liquid capable of dissolving the cellulosic fiber (e.g. ferric sodium tartrate solution) for a prescribed period, thereby removing the fluffs and reducing the volume of the yarn.

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、セルロース系繊維(こ
こでいうセルロース系繊維とは、綿・麻・レーヨン(含
ポリノジック)・キュプラ・精製セルロース系繊維のこ
とで、以下総称してセルロース繊維という。)からなる
糸の処理加工法に関するものである。
BACKGROUND OF THE INVENTION The present invention relates to cellulosic fibers (herein, cellulosic fibers are cotton, hemp, rayon (including polynosic), cupra, and purified cellulosic fibers). ).

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】セルロ
ース系繊維の衣類を洗濯などすると表面が毛羽立ってし
まうので、セルロース系繊維製品は、布とした製品化後
に酸素処理(バイオ処理)により毛羽を除去し、処理後
に洗濯などしても毛羽立ちにくいようにしている。
2. Description of the Related Art Since the surface of a cellulosic fiber product becomes fuzzy when the cellulosic fiber clothing is washed, the cellulosic fiber product is treated with oxygen (bio-treatment) after being made into a cloth. It is removed so that it does not fluff even after washing after treatment.

【0003】しかしながら、この酸素処理は処理時間が
長く、しかもその間微妙な温度管理が必要で非常に厄介
である。
However, this oxygen treatment is very troublesome because it requires a long treatment time and requires delicate temperature control during the treatment.

【0004】本発明は、このような現状に鑑み、研究を
繰り返してセルロースをバイオによらず化学的に溶解で
きる溶解溶液を見い出し、酵素に代わりこの溶液に液浸
することにより短時間で処理でき、しかも製品化したも
のがかたくずれしたりして商品価値が低下するなどを考
慮することなく糸の段階で容易に処理でき、処理作業を
スムーズになし得る秀れたセルロース系繊維からなる糸
の処理加工法を提供するものである。
In view of the above situation, the present invention finds a dissolving solution capable of chemically dissolving cellulose regardless of biotechnology, and treats it in a short time by immersing it in this solution instead of the enzyme. Moreover, a yarn made of excellent cellulosic fibers that can be easily treated at the yarn stage without considering the deterioration of the commercial value due to the product becoming hard and the product value falling. The present invention provides a processing method of.

【0005】[0005]

【課題を解決するための手段】添付図面を参照して本発
明の要旨を説明する。
The gist of the present invention will be described with reference to the accompanying drawings.

【0006】セルロース系繊維の糸を、製品化した後で
はなく糸の段階で、セルロース系繊維を溶解できる能力
をもつ溶解溶液に所定時間だけ液浸して、糸の毛羽を溶
解除去し糸の容量を減量させることを特徴とするセルロ
ース系繊維からなる糸の処理加工法に係るものである。
[0006] The cellulosic fiber yarn is immersed in a dissolving solution capable of dissolving the cellulosic fiber for a predetermined time at a stage of the yarn, not after being commercialized, to dissolve and remove the fluff of the yarn to remove the volume of the yarn. The present invention relates to a method for treating and processing a yarn made of a cellulosic fiber, which is characterized in that

【0007】また、前記溶解溶液として酒石酸鉄IIIナ
トリウム溶液を使用することを特徴とする請求項1記載
のセルロース系繊維からなる糸の処理加工法に係るもの
である。
Further, the present invention relates to the method of processing a yarn made of a cellulosic fiber according to claim 1, characterized in that a sodium iron III tartrate solution is used as the dissolving solution.

【0008】[0008]

【作用】セルロース系繊維の糸を、製品化した後ではな
く糸の段階で、セルロース系繊維を溶解できる能力をも
つ溶解溶液、例えば、酒石酸鉄IIIナトリウム溶液に所
定時間だけ液浸して、糸の毛羽を除去し糸の容量を減量
させる。
The cellulosic fiber yarn is immersed in a dissolving solution having a capability of dissolving the cellulosic fiber, for example, a sodium iron tartrate III solution for a predetermined time at a yarn stage, not after commercialization, to form a yarn. Removes fluff and reduces yarn volume.

【0009】[0009]

【実施例】本実施例では、セルロース系繊維を溶解でき
る能力をもつ溶解溶液として、酒石酸鉄IIIナトリウム
溶液を使用する。以下、この酒石酸鉄IIIナトリウム溶
液について説明する。
EXAMPLE In this example, a sodium ferric tartrate solution is used as a dissolving solution having the ability to dissolve cellulosic fibers. Hereinafter, the iron III tartrate sodium solution will be described.

【0010】1.酒石酸鉄IIIナトリウム(以下EWN
Nという)溶液の調製法 鉄イオン濃度により、以下の方法にしたがってA,Bの
二つの溶液を調製した。
[0010] 1. Iron III tartrate sodium (hereinafter EWN
Method for Preparing Solutions) According to the iron ion concentration, two solutions A and B were prepared according to the following method.

【0011】1−1.調製操作 (1) 酒石酸ナトリウムを水に加えて、煮沸して溶解す
る。溶解したら、20℃程度まで冷やす。
1-1. Preparation procedure (1) Add sodium tartrate to water and dissolve by boiling. Once dissolved, cool to about 20 ° C.

【0012】(2) 水酸化ナトリウムを水に溶かす。溶解
時に発熱するので、これも20℃程度まで冷やす。
(2) Dissolve sodium hydroxide in water. Since heat is generated during melting, this is also cooled to about 20 ° C.

【0013】(3) 塩化第二鉄溶液を水で希釈する。(3) The ferric chloride solution is diluted with water.

【0014】(4) (1)の酒石酸ナトリウム溶液を反応容
器中にあける。反応容器は所定の大きさの容器を一回り
大きな容器にいれて、外側の容器に冷却のため氷水を満
たす。撹拌機のシャフトが通る程度の穴と、薬品を滴下
するための漏斗が通る穴をあけた蓋をして、光が反応容
器中に入らないようにする。
(4) The sodium tartrate solution of (1) is placed in a reaction vessel. As a reaction container, a container of a predetermined size is put in a container that is one size larger, and the outer container is filled with ice water for cooling. A lid with a hole through which the shaft of the stirrer passes and a hole through which a funnel for dropping chemicals passes is used to prevent light from entering the reaction vessel.

【0015】(5) (4)の容器に激しく撹拌しながら、(3)
の塩化第二鉄溶液を徐々に加えて反応させる。
(5) While vigorously stirring in the container of (4), (3)
The ferric chloride solution is gradually added to react.

【0016】(6) (5)に(2)の水酸化ナトリウム水溶液を
徐々に加えて反応させる。
(6) The aqueous sodium hydroxide solution of (2) is gradually added to (5) to react.

【0017】(7) (6)に安定剤として所定量の酒石酸ナ
トリウムを加えて、水で必要な濃度まで希釈する。
(7) A predetermined amount of sodium tartrate is added to (6) as a stabilizer, and diluted with water to a required concentration.

【0018】 1−2.使用薬品量(それぞれ1リットルを調製するために要する薬品量) A.鉄イオン濃度0.18mol/l 酒石酸ナトリウム・2水和物 104 g/200ml水 水酸化ナトリウム 64 g/100ml水 塩化第二鉄溶液(工業用塩化第二鉄) 47ml/160ml水 安定剤(酒石酸ナトリウム・2水和物) 5g B.鉄イオン濃度0.12mol/l 酒石酸ナトリウム・2水和物 69 g/140ml水 水酸化ナトリウム 64 g/100ml水 塩化第二鉄溶液(工業用塩化第二鉄) 31ml/100ml水 安定剤(酒石酸ナトリウム・2水和物) 5g 2.全工程 2−1.(実施例1)綛状の糸による加工 (1) 綛状の糸を調製したEWNN溶液に浸して、5分間
手で振り返し、十分に液が浸透したところで浸漬し、3
0分間放置する。
1-2. Amount of chemicals used (the amount of chemicals required to prepare 1 liter each) Iron ion concentration 0.18 mol / l sodium tartrate dihydrate 104 g / 200 ml water sodium hydroxide 64 g / 100 ml water ferric chloride solution (ferric chloride for industrial use) 47 ml / 160 ml water stabilizer (sodium tartrate・ Dihydrate) 5 g B.I. Iron ion concentration 0.12 mol / l Sodium tartrate dihydrate 69 g / 140 ml Water sodium hydroxide 64 g / 100 ml water Ferric chloride solution (industrial ferric chloride) 31 ml / 100 ml Water Stabilizer (sodium tartrate・ Dihydrate) 5 g 2. All steps 2-1. (Example 1) Processing with a thread-like thread (1) The thread-like thread was dipped in the prepared EWNN solution, turned back by hand for 5 minutes, and dipped when the solution was sufficiently penetrated.
Leave for 0 minutes.

【0019】(2) 浸漬終了後、排液して余分な溶液をき
り、EWNNが分解して水酸化第二鉄の赤い色が現れる
まで水洗する。水洗の排水が着色しなくなったら、0.
1%希硫酸で水酸化第二鉄を除去して脱色させる。
(2) After the immersion, the liquid is drained to remove an excess solution, and washed with water until EWNN is decomposed and a red color of ferric hydroxide appears. If the effluent from the wash is no longer colored,
Decolorize by removing ferric hydroxide with 1% dilute sulfuric acid.

【0020】(3) 水酸化第二鉄が除去されて赤い色がな
くなったら、pH試験紙が中性を示すまで水洗する。
(3) When the red color disappears due to the removal of the ferric hydroxide, the sample is washed with water until the pH test paper becomes neutral.

【0021】(4) 水洗が終了したら、乾燥して製品とす
る。
(4) After washing with water, the product is dried to obtain a product.

【0022】2−2.(実施例2)チーズ状の糸による
加工 (1) チーズ状に巻き上げた糸をチーズ染色機にセットす
る。調製したEWNN溶液を染色機に所定量満たす。2
0℃くらいに冷却しながら液を循環させる。
2-2. (Example 2) Processing with cheese-like yarn (1) The yarn wound up in a cheese-like state is set in a cheese dyeing machine. A prescribed amount of the prepared EWNN solution is filled in a dyeing machine. Two
The liquid is circulated while cooling to about 0 ° C.

【0023】(2) 液を30分間循環させて処理した後、
EWNNが分解して水酸化第二鉄の赤い色が現れるま
で、水をオーバーフローさせながら10分間水洗する。
(2) After circulating the solution for 30 minutes and treating it,
Rinse for 10 minutes while allowing the water to overflow until the EWNN decomposes and the red color of ferric hydroxide appears.

【0024】(3) 水洗の排水が着色しなくなったら、
0.1%希硫酸を満たし、30分間循環させて、水酸化
第二鉄を除去して脱色させる。
(3) If the effluent of the washing is no longer colored,
Fill with 0.1% dilute sulfuric acid and circulate for 30 minutes to remove ferric hydroxide and decolorize.

【0025】(4) 水酸化第二鉄が除去されて糸の赤い色
がなくなったら、pH試験紙が中性を示すまで水洗す
る。
(4) When the ferric hydroxide is removed and the red color of the yarn disappears, the pH test paper is washed with water until neutral.

【0026】(5) 水洗が終了したら、乾燥して製品とす
る。
(5) When the washing is completed, the product is dried to obtain a product.

【0027】3.利点並びに酵素処理との併用の場合の
利点,方法など ○利点 ・微妙な温度管理を要する酵素処理の時間を短縮(従来
60分以上→30分程度)できる。
3. Advantages and advantages, methods, etc. when used in combination with enzyme treatment ○ Advantages ・ Enzyme treatment time that requires delicate temperature control can be shortened (60 minutes or more → about 30 minutes in the past).

【0028】・大きな毛羽は酵素処理で除去できず、強
度が低下するのみであるが、EWNN溶液を使うとこれ
を除去することができる。また、EWNN溶液単独の処
理では小さな毛羽を溶解することで、EWNN溶液の溶
解能を低下させるが、酵素処理を併用して小さな毛羽を
除去しておくことで、EWNN溶液による加工の効果を
向上させることができる。
Large fluff cannot be removed by enzymatic treatment and only the strength is reduced, but it can be removed by using an EWNN solution. In addition, the treatment with the EWNN solution alone dissolves the small fuzz, thereby reducing the dissolving ability of the EWNN solution. However, by removing the small fuzz with the enzyme treatment, the effect of the processing with the EWNN solution is improved. Can be done.

【0029】○方法 ・酵素処理は綛状の糸で噴射式染色機を用いて行う。Method: The enzyme treatment is carried out with a skein-like yarn by using a jet dyeing machine.

【0030】(1) 加工液は酵素(セルラーゼ)濃度5g/
l、酢酸−酢酸ナトリウム緩衝液を用いて、pH5に調
製する。
(1) The processing liquid has an enzyme (cellulase) concentration of 5 g /
l, Adjust to pH 5 using acetic acid-sodium acetate buffer.

【0031】(2) 処理温度は50℃〜60℃で、30分
間処理する。
(2) The treatment temperature is 50 ° C. to 60 ° C. for 30 minutes.

【0032】(3) 処理後、80℃まで加熱して10分間
保ち酵素を失活する。
(3) After the treatment, heat to 80 ° C. and hold for 10 minutes to inactivate the enzyme.

【0033】(4) 失活処理終了後、排水が濁らなくなる
まで水洗する。水洗後、乾燥する。
(4) After completion of the deactivation treatment, the waste water is washed until it does not become cloudy. After washing with water, it is dried.

【0034】・上記酵素処理の後、前述の処理の通りに
EWNN溶液で処理する。
After the above enzyme treatment, treat with the EWNN solution as described above.

【0035】4.EWNN溶液以外に代わるもの EWNN溶液と同様の効果が期待できるものとして、以
下の10点が考えられる。
4. Substitutes other than EWNN solution The following 10 points are considered to be expected to have the same effects as the EWNN solution.

【0036】[0036]

【表1】 [Table 1]

【0037】・上記化合物はEWNN溶液と同様にセル
ロースを溶解する能力がある「セルロース溶媒」として
知られているものである。EWNN溶液は中心金属が3
価の鉄イオンであるが、上記の1aから5bの10点の
中心金属は2価である点が大きな違いである。
The above compounds are known as "cellulose solvents" which have the ability to dissolve cellulose in the same manner as the EWNN solution. The EWNN solution has a central metal of 3
Although it is a valent iron ion, a major difference is that the above-mentioned ten central metals 1a to 5b are divalent.

【0038】・上記の10点はアンモニア、若しくはエ
チレンジアミンを成分としており、液中には遊離のアン
モニア、またはエチレンジアミンを多量に含む。従っ
て、その溶液はアンモニア臭、またはアミン臭が強く、
作業環境をはじめとした周辺環境への影響を考えると完
全に密閉する必要がある。
The above 10 points contain ammonia or ethylenediamine as a component, and the liquid contains a large amount of free ammonia or ethylenediamine. Therefore, the solution has a strong ammonia odor or amine odor,
Considering the impact on the surrounding environment including the working environment, it is necessary to completely seal it.

【0039】・また、上記のものは中心金属がいわゆる
“重金属”であり、廃液の放出は周辺環境の汚染源とな
るため、廃液は完全に回収してなんらかの処理を施す必
要がある。
In the above, the central metal is a so-called "heavy metal", and the discharge of the waste liquid is a source of contamination of the surrounding environment. Therefore, the waste liquid must be completely recovered and subjected to some treatment.

【0040】・安定性についていえば、いずれも空気中
の酸素や温度と言った環境に非常に敏感なので、解放し
た条件で作業できるEWNNに比べて不安定で、産業用
に用いる場合には制限が大きい。
Regarding the stability, all of them are very sensitive to the environment such as oxygen and temperature in the air, so they are more unstable than EWNN which can work under open conditions, and are limited when used for industrial purposes. Is big.

【0041】・1aはキュプラ(銅アンモニアレーヨ
ン)の製造に用いられている。
1a is used for producing cupra (copper ammonia rayon).

【0042】以上より本実施例では酒石酸鉄IIIナトリ
ウム溶液が最適であるとして使用する。
As described above, in the present embodiment, the sodium iron tartrate III solution is used as the optimum.

【0043】[0043]

【発明の効果】本発明によれば、従来時間を要し、しか
もその間微妙な温度管理を要し、厄介なもみなどの操作
が不可欠な酵素処理を行うことなく、単に液浸するだけ
で毛羽を溶解除去できる作業性に秀れたセルロース系繊
維からなる糸の処理加工法となる。
EFFECTS OF THE INVENTION According to the present invention, fluff can be obtained by simply immersing the liquid in the conventional method, which requires a long time, requires delicate temperature control during that time, and does not need an enzyme treatment such as a troublesome operation such as an indispensable operation. It is a method of processing and processing a yarn composed of a cellulosic fiber, which has excellent workability capable of dissolving and removing

【0044】しかも、酵素処理では除去できない大きな
毛羽も除去でき、除去能力に秀れると共に、本発明は糸
段階で処理するため、製品化後に行う場合に比して製品
化後の型崩れや、しわや、縮みなどの心配がなく、また
この意味で糸段階の扱いが容易なため作業性にも秀れた
セルロース系繊維からなる糸の処理加工法となる。
Moreover, large fluff that cannot be removed by the enzyme treatment can be removed, and the removal ability is excellent, and since the present invention treats at the yarn stage, it loses its shape after the product is commercialized as compared with the case where it is carried out after the commercialization. There is no concern about wrinkles or shrinkage, and in this sense the handling of the yarn stage is easy, so it is a processing method for yarn made of cellulosic fibers with excellent workability.

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

【手続補正書】[Procedure amendment]

【提出日】平成7年5月24日[Submission date] May 24, 1995

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0005[Name of item to be corrected] 0005

【補正方法】削除[Correction method] Delete

【手続補正2】[Procedure Amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0006[Correction target item name] 0006

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0006】[0006]

【課題を解決するための手段】セルロース系繊維の糸
を、製品化した後ではなく糸の段階で、セルロース系繊
維を溶解できる能力をもつ溶解溶液に所定時間だけ液浸
して、糸の毛羽を溶解除去し糸の容量を減量させること
を特徴とするセルロース系繊維からなる糸の処理加工法
に係るものである。
[Means for Solving the Problems] The fluff of the yarn is soaked in a dissolving solution having the ability to dissolve the cellulosic fiber for a predetermined time at the stage of the yarn, not after commercialization, of the yarn of the cellulosic fiber. The present invention relates to a method for treating and processing a yarn made of a cellulosic fiber, which is characterized in that the volume of the yarn is reduced by dissolution.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 セルロース系繊維の糸を、製品化した後
ではなく糸の段階で、セルロース系繊維を溶解できる能
力をもつ溶解溶液に所定時間だけ液浸して、糸の毛羽を
溶解除去し糸の容量を減量させることを特徴とするセル
ロース系繊維からなる糸の処理加工法。
1. A fluff of a yarn is dissolved and removed by immersing the yarn of the cellulosic fiber in a dissolving solution having an ability to dissolve the cellulosic fiber for a predetermined time at a stage of the yarn, not after the product is commercialized. A method for treating and processing a yarn made of a cellulosic fiber, characterized in that the volume of the yarn is reduced.
【請求項2】 前記溶解溶液として酒石酸鉄IIIナトリ
ウム溶液を使用することを特徴とする請求項1記載のセ
ルロース系繊維からなる糸の処理加工法。
2. The method of processing a yarn made of a cellulosic fiber according to claim 1, wherein a sodium iron tartrate III solution is used as the dissolution solution.
JP6134536A 1994-06-16 1994-06-16 Processing of yarn made of cellulosic fiber Expired - Fee Related JP2604323B2 (en)

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JP6134536A JP2604323B2 (en) 1994-06-16 1994-06-16 Processing of yarn made of cellulosic fiber

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Application Number Priority Date Filing Date Title
JP6134536A JP2604323B2 (en) 1994-06-16 1994-06-16 Processing of yarn made of cellulosic fiber

Publications (2)

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JPH083869A true JPH083869A (en) 1996-01-09
JP2604323B2 JP2604323B2 (en) 1997-04-30

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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05117966A (en) * 1991-10-24 1993-05-14 Kanebo Ltd Method for producing fabric of pineapple fiber

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05117966A (en) * 1991-10-24 1993-05-14 Kanebo Ltd Method for producing fabric of pineapple fiber

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