JPH0571082A - Bleaching and dyeing of fiber - Google Patents

Bleaching and dyeing of fiber

Info

Publication number
JPH0571082A
JPH0571082A JP3250218A JP25021891A JPH0571082A JP H0571082 A JPH0571082 A JP H0571082A JP 3250218 A JP3250218 A JP 3250218A JP 25021891 A JP25021891 A JP 25021891A JP H0571082 A JPH0571082 A JP H0571082A
Authority
JP
Japan
Prior art keywords
bleaching
bath
dyeing
acid
cloth
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
JP3250218A
Other languages
Japanese (ja)
Other versions
JP3165475B2 (en
Inventor
Terumichi Ohara
熈通 尾原
Akio Ishiwatari
秋夫 石渡
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.)
Kayaku Akzo Corp
Original Assignee
Kayaku Akzo Corp
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 Kayaku Akzo Corp filed Critical Kayaku Akzo Corp
Priority to JP25021891A priority Critical patent/JP3165475B2/en
Publication of JPH0571082A publication Critical patent/JPH0571082A/en
Application granted granted Critical
Publication of JP3165475B2 publication Critical patent/JP3165475B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Treatment Of Fiber Materials (AREA)
  • Coloring (AREA)

Abstract

PURPOSE:To provide a one-bath scouring, bleaching and dyeing process for cotton cloth by simultaneously performing the scorching and bleaching of the cloth, dyeing the cloth in the same bath without discharging the bath and subjecting the dyed cloth to conventional washing and drying. CONSTITUTION:In the scouring and bleaching of a cotton cloth, a peracid is added together with conventional scouring agent and ion-sequestering agent to a bath and the bath is heated to effect the scouring and bleaching of the cloth. A halogenic acid salt is added to the same bath to effect the complete decomposition of the peracid, a reactive dye is added to the bath and the cloth is dyed by conventional method. A number of washing and neutralizing steps necessary in conventional process after the scouring and bleaching process and before the dyeing process become unnecessary in the present process to enable the reduction of time and energy.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は繊維の漂白染色法に関す
る。
FIELD OF THE INVENTION The present invention relates to a bleaching and dyeing method for fibers.

【0002】[0002]

【従来の技術】木綿、麻、レーヨン等のセルロース繊維
の染色は、特に鮮明度を得るため精練のあと、次亜塩素
酸ナトリウムや過酸化水素等の塩素系または酸素系の漂
白剤を用いて下晒しをしたあと、還元、中和ないしは水
洗により漂白剤を除去しその後で染色するという工程が
通常行なわれている。そしてこの方法では、下晒しおよ
び漂白剤の除去並びに反応性染料による染色後のソーピ
ング工程に多大の時間とエネルギーを必要としている。
2. Description of the Related Art Dyeing of cellulose fibers such as cotton, hemp and rayon is performed by scouring for obtaining a sharpness and then using a chlorine-based or oxygen-based bleaching agent such as sodium hypochlorite and hydrogen peroxide. The steps of performing bleaching under exposure, reducing, neutralizing or washing with water to remove the bleaching agent, and then dyeing are usually performed. And this method requires a great deal of time and energy for the under-exposure and removal of the bleaching agent and the soaping step after dyeing with the reactive dye.

【0003】[0003]

【発明が解決しようとする課題】反応性染料による染色
の前に繊維の漂白を行うことにより漂白効果を得ると共
に、同浴に於いて染色を行うことにより工程の簡略化、
工程短縮を行うことにあり、またこれを可能にならしめ
るため新規な方法と繊維の漂白染色剤が求められてい
る。
The bleaching effect is obtained by bleaching the fiber before dyeing with the reactive dye, and the process is simplified by dyeing in the same bath.
There is a need for new methods and bleach dyes for fibers in order to shorten the process and to make this possible.

【0004】[0004]

【課題を解決するための手段】本発明者等は、すでに染
料は破壊せずに繊維中の不純物からなる色のみを漂白で
きる漂白剤を見いだし、染色漂白剤及び染色漂白法とし
て特許申請している(特願平2−325442)が、こ
の特許記載の方法では使用出来る染料に制限がある。
The present inventors have already found a bleaching agent capable of bleaching only a color consisting of impurities in fibers without destroying the dye, and applied for a patent as a dyeing bleaching agent and a dyeing bleaching method. (Japanese Patent Application No. 2-325442), the dyes that can be used in the method described in this patent are limited.

【0005】染色に入る前に、漂白剤を完全に無くして
しまえば漂白剤の影響が無くなり、使用出来る染料に制
限なく同浴で染色に入れ、漂白液の抜取り、漂白剤の洗
浄という工程が省け、合理化が出来ると考えて鋭意研究
の結果、ある特定の染色漂白剤とある特定の添加剤との
組合せにより、この目的を達成出来ることを見出し本発
明に到った。
Before the dyeing, if the bleaching agent is completely removed, the effect of the bleaching agent disappears, and there is no limit to the dyes that can be used, and the steps of dyeing in the same bath, removing the bleaching solution, and washing the bleaching agent are carried out. As a result of earnest research that it can be omitted and rationalized, the inventors have found that this object can be achieved by a combination of a specific dye bleaching agent and a specific additive, and arrived at the present invention.

【0006】即ち本発明は次の(1)及び(2)からな
る。 (1)繊維を染色するに際し、下記一般式(1)で表わ
される有機過酸またはそれらの塩もしくは錯体からなる
漂白剤で漂白し、引き続き下記一般式(2)で表わされ
る塩を使用して漂白剤を分解し、漂白後浴を排出するこ
となく、引き続いて染色を施すことを特徴とする繊維の
漂白染色法。 一般式(1)
That is, the present invention comprises the following (1) and (2). (1) When dyeing the fiber, bleaching with a bleaching agent consisting of an organic peracid represented by the following general formula (1) or a salt or complex thereof, and then using a salt represented by the following general formula (2) A bleaching and dyeing method for fibers, which is characterized by decomposing a bleaching agent and subsequently dyeing without discharging the bath after bleaching. General formula (1)

【0007】[0007]

【化2】 [Chemical 2]

【0008】(但し、Rは置換または非置換のアルキル
基、アリル基またはアラルキル基、nは1〜6の自然数
を示す。) 一般式(2) R1 X (但し、R1 は金属イオン又は置換または非置換の4級
アンモニウム基を示し、Xはハロゲンイオンを示す。)
(Wherein R is a substituted or unsubstituted alkyl group, an allyl group or an aralkyl group, n is a natural number of 1 to 6) General formula (2) R 1 X (where R 1 is a metal ion or (This represents a substituted or unsubstituted quaternary ammonium group, and X represents a halogen ion.)

【0009】(2)繊維がセルロース繊維単独またはそ
の他の繊維と混合したセルロース繊維である(1)記載
の繊維の漂白染色法。
(2) The bleaching dyeing method for fibers according to (1), wherein the fibers are cellulose fibers alone or mixed with other fibers.

【0010】本発明の繊維の染色漂白剤である一般式
(1)で表わされる有機過酸またはその塩(金属塩又は
アンモニウム塩)の具体例としては過蟻酸、過酢酸、過
プロピオン酸、過クロル酢酸、過トリフルオロ酢酸、過
ブチル酸、過カプリル酸、過ラウリン酸、ジ過こはく
酸、ジ過グルタル酸、ジ過アジピン酸、モノ過ノナン二
酸、ジ過ノナン二酸、モノ過デカン二酸、ジ過デカン二
酸、モノ過ドデカン二酸、ジ過ドデカン二酸、モノ過ウ
ンデカン二酸、ジ過ウンデカン二酸、ジ過フタル酸、ジ
過テレフタル酸、過安息香酸、m−クロロ過安息香酸、
2,4−ジクロロ過安息香酸、モノ過フタル酸、モノ過
フタル酸マグネシウム、モノ過こはく酸、モノ過こはく
酸マグネシウム、モノ過マレイン酸、モノ過マレイン酸
カルシウム、モノ過グルタル酸、モノ過グルタル酸マグ
ネシウム、過トリメリット酸、過ピロメリット酸等が挙
げられる。特に好ましくはモノ過フタル酸マグネシウム
及びジ過ドデカン二酸である。
Specific examples of the organic peracids represented by the general formula (1) or salts thereof (metal salts or ammonium salts) which are the dye-bleaching agents for fibers of the present invention include performic acid, peracetic acid, perpropionic acid and Chloracetic acid, pertrifluoroacetic acid, perbutyric acid, percaprylic acid, perlauric acid, dipersuccinic acid, diperglutaric acid, diperadipic acid, monopernonanedioic acid, dipernonanedioic acid, monoperdecane. Diacid, diperdecanedioic acid, monoperdodecanedioic acid, diperdodecanedioic acid, monoperundecanedioic acid, diperundecanedioic acid, diperphthalic acid, diperterephthalic acid, perbenzoic acid, m-chloro Perbenzoic acid,
2,4-dichloroperbenzoic acid, monoperphthalic acid, magnesium monoperphthalate, monopersuccinic acid, magnesium monopersuccinate, monopermaleic acid, calcium monopermaleate, monoperglutaric acid, monoperglutal Magnesium acid, pertrimellitic acid, perpyromellitic acid and the like can be mentioned. Particularly preferred are magnesium monoperphthalate and diperdodecanedioic acid.

【0011】漂白浴中の漂白剤の濃度は、有効活性酸素
量で好ましくは0.05〜10% o.w.f. 特に好ましく
は0.3〜5% o.w.f. である。
The concentration of the bleaching agent in the bleaching bath is preferably 0.05 to 10% owf, particularly preferably 0.3 to 5% owf in terms of the amount of effective active oxygen.

【0012】pHは好ましくは1〜14、特に好ましく
は2〜10である。漂白浴の温度は好ましくは20〜1
10℃特に好ましくは40〜90℃である。
The pH is preferably 1-14, particularly preferably 2-10. The temperature of the bleaching bath is preferably 20 to 1
The temperature is particularly preferably 10 ° C and 40 to 90 ° C.

【0013】漂白剤を分解する塩の金属イオンとなる金
属は、ナトリウム、カリウム、リチウム、銅、アルミニ
ウム、マグネシウム、カルシウム、亜鉛、バリウム、
錫、鉄、コバルト、ニッケル等であり、漂白剤を分解す
る塩の置換または非置換の4級アンモニウム基は、アン
モニウム基、モノメチルアンモニウム基、ジメチルアン
モニウム基、トリメチルアンモニウム基、テトラメチル
アンモニウム基、モノエチルアンモニウム基、ジエチル
アンモニウム基、トリエチルアンモニウム基、モノメチ
ルトリエチルアンモニウム基、テトラエチルアンモニウ
ム基等のアンモニウム基であり、更に高級のアルキル
基、アリル基またはアラルキル基で置換されていてもよ
いアンモニウム基である。漂白剤を分解する塩のハロゲ
ンイオンは、フッ素イオン、塩素イオン、臭素イオン、
沃素イオンである。また4級アンモニュウム基とハロゲ
ンイオンの塩は置換又は非置換アミンとハロゲン酸とか
ら作られてもよい。特に好ましい塩は、食塩、臭化カリ
ウム、塩化アンモニウム等である。
The metal which becomes the metal ion of the salt decomposing the bleaching agent is sodium, potassium, lithium, copper, aluminum, magnesium, calcium, zinc, barium,
The substituted or unsubstituted quaternary ammonium group of the salt that decomposes the bleaching agent is tin, iron, cobalt, nickel, etc., and examples thereof include an ammonium group, a monomethylammonium group, a dimethylammonium group, a trimethylammonium group, a tetramethylammonium group, and a monomethylammonium group. It is an ammonium group such as an ethylammonium group, a diethylammonium group, a triethylammonium group, a monomethyltriethylammonium group and a tetraethylammonium group, and an ammonium group which may be substituted with a higher alkyl group, an allyl group or an aralkyl group. The halogen ion of the salt that decomposes the bleach is fluoride ion, chlorine ion, bromine ion,
It is an iodine ion. Also, the salt of a quaternary ammonium group and a halogen ion may be made from a substituted or unsubstituted amine and a halogen acid. Particularly preferred salts are common salt, potassium bromide, ammonium chloride and the like.

【0014】漂白剤を分解するに際し、使用される塩の
濃度は0.05〜10重量%であり、特に好ましくは
0.3〜5重量%である。
In decomposing the bleaching agent, the concentration of the salt used is 0.05 to 10% by weight, particularly preferably 0.3 to 5% by weight.

【0015】漂白剤を分解するに際し、使用される温度
は20〜110℃特に好ましくは40〜90℃である。
When decomposing the bleaching agent, the temperature used is 20 to 110 ° C, particularly preferably 40 to 90 ° C.

【0016】本発明に適用される染料は一般に市販され
ている種々の染料が挙げられ、特に反応性染料が好まし
く、使用量及び染色法はそれら市販品の摘要基準にした
がって行う。代表的な反応性染料の例としては、カヤシ
オン(日本化薬)、レマゾール(ヘキスト)、プロシオ
ン(ICI)、ダイアミラ(三菱化成)、セルマゾール
(三井東圧化学)、スミフィックス(住友化学)、シバ
クロン(CIBA)、レバフィックス(バイエル)、フ
ィクサゾール(大東化学)等が挙げられる。
The dyes applicable to the present invention include various dyes which are generally commercially available, and reactive dyes are particularly preferable, and the amount used and the dyeing method are carried out according to the summary standard of those commercially available products. Examples of representative reactive dyes include cocoyone (Nippon Kayaku), remazole (Hoechst), procion (ICI), diamira (Mitsubishi Kasei), selmazole (Mitsui Toatsu Chemical), Sumifix (Sumitomo Chemical), Cibacron. (CIBA), Levafix (Bayer), Fixazole (Daito Kagaku) and the like.

【0017】本発明の漂白剤及び漂白剤を分解する塩は
使用時におけるpHを有効成分の最適pH域に保つため
のpH調節剤例えば、酢酸、メタケイ酸ナトリウム、炭
酸ナトリウム又は炭酸水素ナトリウムを好ましくは0〜
40%、有効成分の水中金属イオンによる接触分解を抑
制するための金属イオン封止剤例えばカヤキレーターC
−1000、エチレンジアミン四酢酸又はディクエスト
2010(三菱モンサント化成(株)製)を好ましくは
0〜1%、染色助剤例えば食塩又は硫酸ナトリウムを好
ましくは0〜98%及び取り扱いや安定性を良くするた
めの希釈剤例えば水、有機溶剤、セライト又は超微粒子
状無水シリカを漂白剤1部及び/又は漂白剤を分解する
塩1部に対し好ましくは0〜100部含むことができ
る。
The bleaching agent and the salt that decomposes the bleaching agent of the present invention are preferably pH adjusters for maintaining the pH at the time of use in the optimum pH range of the active ingredient, such as acetic acid, sodium metasilicate, sodium carbonate or sodium hydrogen carbonate. Is 0
40%, a metal ion sealant for suppressing the catalytic decomposition of the active ingredient by metal ions in water, for example, Kayachelator C
-1000, ethylenediaminetetraacetic acid or Dequest 2010 (manufactured by Mitsubishi Monsanto Kasei Co., Ltd.) is preferably 0 to 1%, a dyeing aid such as sodium chloride or sodium sulfate is preferably 0 to 98%, and handling and stability are improved. A diluent for use such as water, an organic solvent, Celite or ultrafine particulate anhydrous silica can be preferably contained in an amount of 0 to 100 parts with respect to 1 part of the bleaching agent and / or 1 part of the salt decomposing the bleaching agent.

【0018】本発明の漂白剤及び漂白剤を分解する塩は
染色法に応じて溶液、懸濁液、ペーストあるいは粉末状
等どのような形態でもとることができる。
The bleaching agent and the salt decomposing the bleaching agent of the present invention can be in any form such as a solution, suspension, paste or powder depending on the dyeing method.

【0019】[0019]

【作 用】本発明の染色漂白剤及び漂白剤を分解する塩
を使用すれば繊維の染色漂白に当たって漂白を先に行
い、漂白後漂白剤を分解する事により排出操作或いはす
すぎ洗い操作を省いて染色することが可能である。通常
の下晒し後染色する方法と同等もしくはそれ以上の漂白
効果を得ることが可能である。
[Working] If the dye bleaching agent of the present invention and a salt decomposing the bleaching agent are used, the bleaching is performed before dyeing and bleaching the fiber, and the bleaching agent is decomposed after the bleaching, thereby eliminating the discharge operation or the rinse operation. It is possible to dye. It is possible to obtain a bleaching effect equal to or higher than that of the usual method of dyeing after bleaching.

【0020】[0020]

【実施例】次に本発明をより充分に理解せしめるために
実施例を示すが、これらの実施例は例証のためのもので
あって、本発明を限定するものではない。
EXAMPLES Examples will now be shown in order to more fully understand the present invention, but these examples are for the purpose of illustration and not for limiting the present invention.

【0021】まず実施例1では、最も一般的な漂白剤で
ある過酸化水素(比較例1−1)及び次亜塩素酸ナトリ
ウム(比較例1−2)と比較することにより本発明の漂
白剤の漂白能及び染色に与える影響を評価した。
First, in Example 1, the bleaching agent of the present invention was compared with hydrogen peroxide (Comparative Example 1-1) and sodium hypochlorite (Comparative Example 1-2), which are the most common bleaching agents. Was evaluated for its effect on bleaching ability and dyeing.

【0022】実施例2において他種属の染料による例を
示した。また実施例3〜4に混紡についての例を示し
た。
In Example 2, an example using a dye of another genus was shown. Examples of mixed spinning are shown in Examples 3 to 4.

【0023】実施例1.精練後晒しをしていない未染色
の木綿布(以後未染色布と表記する)をまず最初に以下
に示す実施例1−1〜4に示した組成をもつ浴中で80
℃の温度で20分間処理し漂白した。引き続いて浴を排
出することなく食塩10g/lを加え90℃に昇温し2
0分間処理した。更に浴を排出することなく80℃に下
げ次の染色薬剤のうち染料と無水硫酸ナトリウムを加え
て同温度で10分間処理した。続いて炭酸ナトリウムを
加えて同温度で1時間染色した。染色後すすぎ洗いし、
ついで98℃の石鹸水で15分間洗浄した。浴中の繊維
対漂白浴及び染色浴の比はいずれも1:15である。
Example 1. An undyed cotton cloth which has not been exposed after scouring (hereinafter referred to as an undyed cloth) is firstly put in a bath having the composition shown in Examples 1-1 to 4 below.
It was treated at a temperature of ° C for 20 minutes and bleached. Then, add 10 g / l of salt without discharging the bath and raise the temperature to 90 ° C.
It was processed for 0 minutes. Further, without discharging the bath, the temperature was lowered to 80 ° C., a dye and an anhydrous sodium sulfate among the following dyeing agents were added, and the mixture was treated at the same temperature for 10 minutes. Subsequently, sodium carbonate was added and dyeing was carried out at the same temperature for 1 hour. Rinse after dyeing,
Then, it was washed with soapy water at 98 ° C. for 15 minutes. The ratio of fiber to bleaching bath and dyeing bath in the bath is 1:15.

【0024】 カヤシオンブルーE−CN 2 %o.w.f. 無水硫酸ナトリウム 100 g/l 炭酸ナトリウム 20 g/lKayashion Blue E-CN 2% o. w. f. Anhydrous sodium sulfate 100 g / l Sodium carbonate 20 g / l

【0025】実施例1−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l (日本化薬(株)製金属イオン封止剤) 40%過酢酸 2 g/lExample 1-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l (Nippon Kayaku Co., Ltd. metal ion sealant) 40% peracetic acid 2 g / L

【0026】実施例1−2 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 27%ジ過ドデカン二酸 2.3g/lExample 1-2 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l 27% diperdodecanedioic acid 2.3 g / l

【0027】実施例1−3 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l H−48 15.6g/l (日本パーオキサイド(株)製モノ過フタル酸マグネシ
ウム、有効酸素4.9%)
Example 1-3 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l H-48 15.6 g / l (Nippon Peroxide Co., Ltd. magnesium monoperphthalate, available oxygen 4. 9%)

【0028】実施例1−4 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 過安息香酸 1 g/lExamples 1-4 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l Perbenzoic acid 1 g / l

【0029】比較例1.未染色布を実施例1と同じく比
較例1−1及び比較例1−2に示した組成の漂白浴中
で、実施例1と同一条件で漂白した。引き続いて実施例
1と同一の染色薬剤を用いて、実施例1と同一条件で染
色処理を施した。
Comparative Example 1. The undyed cloth was bleached under the same conditions as in Example 1 in a bleaching bath having the compositions shown in Comparative Examples 1-1 and 1-2, as in Example 1. Subsequently, using the same dyeing agent as in Example 1, dyeing treatment was performed under the same conditions as in Example 1.

【0030】比較例1−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/lComparative Example 1-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l

【0031】比較例1−2 12%次亜塩素酸ナトリウム 0.9g/lComparative Example 1-2 12% sodium hypochlorite 0.9 g / l

【0032】比較例2.未染色布を実施例1−2と同一
条件で漂白し、その後90℃での食塩処理を行うことな
く、引き続いて実施例1と同一の染色薬剤を用いて、実
施例1と同一条件で染色処理を施した。(特願平2−3
25442の方法に相当する。)
Comparative Example 2. The undyed cloth was bleached under the same conditions as in Example 1-2, and subsequently dyed under the same conditions as in Example 1 using the same dyeing agent as in Example 1 without performing salt treatment at 90 ° C. Treated. (Japanese Patent Application 2-3
This corresponds to the method of 25442. )

【0033】 漂白能○:充分な漂白能あり △:漂白能不充分 ×:漂白能ほとんどなし ××:漂白能全くなし 鮮明度○:実用に耐える △:僅かに色落ちあ
り ×:かなりの色落ちあり ××:著しい色落ちあり
[0033] Bleaching ability ○: Sufficient bleaching ability △: Inadequate bleaching ability ×: Almost no bleaching ability × ×: No bleaching ability Sharpness ○: Practical use △: Slight discoloration ×: Significant discoloration × X: There is remarkable discoloration

【0034】比較例3.未染色布をまず最初に次の組成
を持つ浴中で80℃の温度で20分間処理し漂白した。 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/l 漂白後、浴を排出しそして繊維材料を冷水で注意深くす
すぎ洗いし、その後次の染色薬剤組成のうち染料と無水
硫酸ナトリウムを加えた浴中で80℃の温度で10分間
処理した。続いて炭酸ナトリウムを加えて同じく同温度
で1時間染色した。
Comparative Example 3. The undyed fabric is first bleached by treating it at a temperature of 80 ° C. for 20 minutes in a bath having the following composition: Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l After bleaching, the bath is drained and the fiber material is carefully rinsed with cold water, Then, it was treated for 10 minutes at a temperature of 80 ° C. in a bath containing a dye and an anhydrous sodium sulfate among the following dyeing chemical compositions. Subsequently, sodium carbonate was added and dyeing was carried out at the same temperature for 1 hour.

【0035】 カヤシオンブルーE−CN 2 %o.w.f. 無水硫酸ナトリウム 100 g/l 炭酸ナトリウム 20 g/l 染色後すすぎ洗いし、ついで98℃の石鹸水で15分間
洗浄した。なお繊維対漂白浴及び染色浴の比はいずれも
1:15である。通常の優れた染色物が得られた。
Kayashi On Blue E-CN 2% o. w. f. Anhydrous sodium sulfate 100 g / l Sodium carbonate 20 g / l After dyeing, it was rinsed and then washed with soapy water at 98 ° C. for 15 minutes. The ratio of fiber to bleaching bath and dyeing bath is 1:15. The usual excellent dyeings were obtained.

【0036】実施例2.未染色布をまず最初に以下に示
す実施例2−1〜3に示した組成をもつ浴中で80℃の
温度で30分間処理し漂白した。引き続いて浴を排出す
ることなく臭化カリウム(KBr)10g/lを加え9
0℃に昇温し20分間処理した。更に引き続いて浴を排
出することなく60℃にし次の染色薬剤のうち染料と無
水硫酸ナトリウムを加えて同温度で10分間処理した。
続いて結晶リン酸三ナトリウムを加えて同温度で1時間
染色した。染色後注意深く水洗し陰干しして乾燥した。
浴中の繊維対漂白浴及び染色浴の比はいずれも1:15
である。 ダイヤミラターキスブルーG 2 %o.w.f. 無水硫酸ナトリウム 50 g/l 結晶リン酸三ナトリウム 20 g/l
Example 2. The undyed fabric was first bleached by treating it for 30 minutes at a temperature of 80 ° C. in a bath having the composition given in Examples 2-1 to 3 below. Subsequently, 10 g / l of potassium bromide (KBr) was added without draining the bath, and 9
The temperature was raised to 0 ° C. and the treatment was performed for 20 minutes. Subsequently, the bath was discharged to 60 ° C. without discharging it, and a dye and anhydrous sodium sulfate were added to the following dyeing agents and the mixture was treated at the same temperature for 10 minutes.
Subsequently, crystalline trisodium phosphate was added and dyeing was carried out at the same temperature for 1 hour. After dyeing, it was washed carefully with water, dried in the shade and dried.
The ratio of fiber in the bath to bleaching bath and dyeing bath is 1:15
Is. Diamira Turkis Blue G 2% o. w. f. Anhydrous sodium sulfate 50 g / l Crystalline trisodium phosphate 20 g / l

【0037】実施例2−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 40%過酢酸 2 g/lExample 2-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 40% peracetic acid 2 g / l

【0038】実施例2−2 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 27%ジ過ドデカン二酸 2.3g/lExample 2-2 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l 27% diperdodecanedioic acid 2.3 g / l

【0039】実施例2−3 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l H−48 15.6g/lExample 2-3 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l H-48 15.6 g / l

【0040】比較例4.未染色布を実施例2と同じく比
較例4−1及び比較例4−2に示した組成の漂白浴中
で、実施例2と同一条件で漂白した。引き続いて実施例
2と同一の染色薬剤を用いて、実施例2と同一条件で染
色処理を施した。
Comparative Example 4. The undyed cloth was bleached under the same conditions as in Example 2 in a bleaching bath having the composition shown in Comparative Example 4-1 and Comparative Example 4-2 as in Example 2. Subsequently, the same dyeing agent as in Example 2 was used, and dyeing treatment was performed under the same conditions as in Example 2.

【0041】比較例4−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/lComparative Example 4-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l

【0042】比較例4−2 12%次亜塩素酸ナトリウム 0.9g/l 漂白能○:充分な漂白能あり △:漂白能不充分 ×:漂白能ほとんどなし ××:漂白能全くなし 鮮明度○:実用に耐える △:僅かに色落ちあ
り ×:かなりの色落ちあり ××:著しい色落ちあり
Comparative Example 4-2 12% Sodium Hypochlorite 0.9 g / l Bleaching ability ○: Sufficient bleaching ability △: Inadequate bleaching ability ×: Almost no bleaching ability × ×: No bleaching ability Sharpness ○: Practical use Δ: Slight discoloration ×: Significant discoloration × X: There is remarkable discoloration

【0043】実施例3 未染色の木綿とアクリルの50:50の混紡の布(以後
未染色アクリル混紡布と表記する)をまず最初に次に示
す染色薬剤組成の浴中で98℃で1時間染色した。 カヤクリルライトブルー4GSL−ED 1 %o.w.f. 酢酸 0.5 g/l
Example 3 A 50:50 blended fabric of undyed cotton and acrylic (hereinafter referred to as undyed acrylic blended fabric) is first of all in a bath of the following dyeing agent composition at 98 ° C. for 1 hour. Stained. Kayacryl light blue 4GSL-ED 1% o. w. f. Acetic acid 0.5 g / l

【0044】次いで浴を排出することなく80℃まで降
温し、以下に示す実施例3−1〜3に示した組成をもつ
浴中で80℃の温度で20分間処理し漂白した。引き続
いて浴を排出することなく食塩10g/lを加え90℃
に昇温し20分間処理した。更に引き続いて浴を排出す
ることなく80℃に下げ次の染色薬剤のうち染料と無水
硫酸ナトリウムを加えて同温度で10分間処理した。続
いて炭酸ナトリウムを加えて同温度で1時間染色した。 カヤシオンターキスE−A 1 %o.w.f. 無水硫酸ナトリウム 100 g/l 炭酸ナトリウム 20 g/l 染色後水洗し、ついで80℃のデモールN 2g/l
(株式会社花王の製品)の浴で15分間洗浄した。浴中
の繊維対漂白浴及び染色浴の比はいずれも1:15であ
る。
Next, the temperature was lowered to 80 ° C. without discharging the bath, and the mixture was treated at a temperature of 80 ° C. for 20 minutes in a bath having the composition shown in the following Examples 3-1 to 3 to bleach. Subsequently, add 10 g / l of salt without discharging the bath, and the temperature is 90 ° C.
The temperature was raised to 20 ° C. and treated for 20 minutes. Subsequently, the bath was discharged to 80 ° C. without discharging, and the following dyeing agents, dye and anhydrous sodium sulfate were added, and the mixture was treated at the same temperature for 10 minutes. Subsequently, sodium carbonate was added and dyeing was carried out at the same temperature for 1 hour. Kayashi Onturkis EA 1% o. w. f. Anhydrous sodium sulfate 100 g / l Sodium carbonate 20 g / l After dyeing, washing with water, then 80 ° C. demol N 2 g / l
It was washed in a bath (product of Kao Corporation) for 15 minutes. The ratio of fiber to bleaching bath and dyeing bath in the bath is 1:15.

【0045】実施例3−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 40%過酢酸 2 g/lExample 3-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 40% peracetic acid 2 g / l

【0046】実施例3−2 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 27%ジ過ドデカン二酸 2.3g/lExample 3-2 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l 27% diperdodecanedioic acid 2.3 g / l

【0047】実施例3−3 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l H−48 15.6g/lExample 3-3 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l H-48 15.6 g / l

【0048】比較例5.未染色アクリル混紡布を実施例
3と同じくカヤクリルライトブルー4GSL−EDで染
色し、比較例4−1及び比較例4−2に示した組成の漂
白浴中で、実施例3と同一条件で漂白した。引き続いて
実施例3と同一の染色薬剤を用いて、実施例3と同一条
件で染色処理を施した。
Comparative Example 5. Undyed acrylic blended fabric was dyed with Kayacryl Light Blue 4GSL-ED as in Example 3, and the same conditions as in Example 3 were applied in a bleaching bath having the composition shown in Comparative Examples 4-1 and 4-2. Bleached. Subsequently, using the same dyeing agent as in Example 3, dyeing treatment was performed under the same conditions as in Example 3.

【0049】比較例5−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/lComparative Example 5-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l

【0050】比較例5−2 12%次亜塩素酸ナトリウム 0.9g/l 漂白能○:充分な漂白能あり △:漂白能不充分 ×:漂白能ほとんどなし ××:漂白能全くなし 鮮明度○:実用に耐える △:僅かに色落ちあ
り ×:かなりの色落ちあり ××:著しい色落ちあり
Comparative Example 5-2 12% Sodium hypochlorite 0.9 g / l Bleaching ability ○: Sufficient bleaching ability △: Inadequate bleaching ability ×: Almost no bleaching ability × ×: No bleaching ability Sharpness ○: Practical use Δ: Slight discoloration ×: Significant discoloration × X: There is remarkable discoloration

【0051】実施例4.未染色の木綿とポリエステルの
50:50の混紡の布(以後未染色ポリエステル混紡布
と表記する)をまず最初に耐圧容器中次に示す染色薬剤
組成の浴中で130℃で1時間染色した。 カヤセロンターキスE−GL 1 %o.w.f. 酢酸 0.45 g/l 酢酸ナトリウム(3水塩) 0.55 g/l
Example 4. A 50:50 blended fabric of undyed cotton and polyester (hereinafter referred to as undyed polyester blended fabric) was first dyed in a pressure vessel at 130 ° C. for 1 hour in a bath having the following dyeing agent composition. Kayaceron Turkis E-GL 1% o. w. f. Acetic acid 0.45 g / l Sodium acetate (trihydrate) 0.55 g / l

【0052】次いで浴を排出することなく80℃まで降
温し、以下に示す実施例4−1〜3に示した組成をもつ
浴中で80℃の温度で20分間処理し漂白した。引き続
いて浴を排出することなく食塩10g/lを加え90℃
に昇温し20分間処理した。更に引き続いて浴を排出す
ることなく80℃に下げ次の染色薬剤のうち染料と無水
硫酸ナトリウムを加えて同温度で10分間処理した。続
いて炭酸ナトリウムを加えて同温度で1時間染色した。 カヤシオンターキスE−A 1 %o.w.f. 無水硫酸ナトリウム 100 g/l 炭酸ナトリウム 20 g/l 染色後水洗し、ついで98℃の石鹸水で15分間洗浄し
た。浴中の繊維対漂白浴及び染色浴の比はいずれも1:
15である。
Next, the temperature of the bath was lowered to 80 ° C. without discharging it, and the mixture was treated at a temperature of 80 ° C. for 20 minutes in a bath having the composition shown in the following Examples 4-1 to bleaching. Subsequently, add 10 g / l of salt without discharging the bath, and the temperature is 90 ° C.
The temperature was raised to 20 ° C. and treated for 20 minutes. Subsequently, the bath was discharged to 80 ° C. without discharging, and the following dyeing agents, dye and anhydrous sodium sulfate were added, and the mixture was treated at the same temperature for 10 minutes. Subsequently, sodium carbonate was added and dyeing was carried out at the same temperature for 1 hour. Kayashi Onturkis EA 1% o. w. f. Anhydrous sodium sulfate 100 g / l Sodium carbonate 20 g / l After dyeing, it was washed with water and then with soapy water at 98 ° C. for 15 minutes. The ratio of fiber to bleaching bath and dyeing bath in the bath is 1:
It is 15.

【0053】実施例4−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 40%過酢酸 2 g/lExample 4-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 40% peracetic acid 2 g / l

【0054】実施例4−2 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 27%ジ過ドデカン二酸 2.3g/lExample 4-2 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l 27% Diperdodecanedioic acid 2.3 g / l

【0055】実施例4−3 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l H−48 15.6g/lExample 4-3 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l H-48 15.6 g / l

【0056】比較例6.未染色ポリエステル混紡布をま
ず最初に耐圧容器中次に示す染色薬剤組成の浴中で13
0℃で1時間染色した。 カヤセロンターキスE−GL 1 %o.w.f. 酢酸 0.45 g/l 酢酸ナトリウム(3水塩) 0.55 g/l 次いで浴を排出することなく80℃まで降温し、実施例
4と同じく比較例5−1及び比較例5−2に示した組成
の漂白浴中で、実施例4と同一条件で漂白した。引き続
いて実施例4と同一の染色薬剤を用いて、実施例4と同
一条件で染色処理を施した。
Comparative Example 6. The undyed polyester blended fabric is first placed in a pressure resistant container in a bath of the following dyeing agent composition.
Staining was performed at 0 ° C for 1 hour. Kayaceron Turkis E-GL 1% o. w. f. Acetic acid 0.45 g / l Sodium acetate (trihydrate) 0.55 g / l Then, the temperature was lowered to 80 ° C. without discharging the bath, and Comparative Example 5-1 and Comparative Example 5-2 were carried out similarly to Example 4. Bleaching was performed under the same conditions as in Example 4 in a bleaching bath having the composition shown. Subsequently, using the same dyeing agent as in Example 4, dyeing treatment was performed under the same conditions as in Example 4.

【0057】比較例6−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/lComparative Example 6-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l

【0058】比較例6−2 12%次亜塩素酸ナトリウム 0.9g/l 漂白能○:充分な漂白能あり △:漂白能不充分 ×:漂白能ほとんどなし ××:漂白能全くなし 鮮明度○:実用に耐える △:僅かに色落ちあ
り ×:かなりの色落ちあり ××:著しい色落ちあり
Comparative Example 6-2 12% sodium hypochlorite 0.9 g / l Bleaching ability ○: Sufficient bleaching ability △: Inadequate bleaching ability ×: Almost no bleaching ability × ×: No bleaching ability Sharpness ○: Practical use Δ: Slight discoloration ×: Significant discoloration × X: There is remarkable discoloration

【0059】[0059]

【発明の効果】本発明の染色漂白剤を使用すると繊維の
漂白工程と染色工程との間に従来必要であった排出操作
及び/又は洗浄の回数を減らし且つ水及び加熱のための
熱量の節約、洗浄及び/又は排出に要する時間の節約、
水処理に関する改善などを得ることができる。
The use of the dye bleaching agent of the present invention reduces the number of discharge operations and / or washings conventionally required between the fiber bleaching step and the dyeing step, and saves the amount of heat for water and heating. Save time for cleaning and / or draining,
You can get the improvement about water treatment.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】繊維を染色するに際し、下記一般式(1)
で表わされる有機過酸またはそれらの塩もしくは錯体か
らなる漂白剤で漂白し、引き続き下記一般式(2)で表
わされる塩を使用して漂白剤を分解し、漂白後浴を排出
することなく、引き続いて染色を施すことを特徴とする
繊維の漂白染色法。 一般式(1) 【化1】 (但し、Rは置換または非置換のアルキル基、アリル基
またはアラルキル基、nは1〜6の自然数を示す。) 一般式(2) R1 X (但し、R1 は金属イオン又は置換または非置換の4級
アンモニウム基を示し、Xはハロゲンイオンを示す。)
1. When dyeing a fiber, the following general formula (1) is used.
Bleaching with a bleaching agent consisting of an organic peracid represented by or a salt or complex thereof, followed by decomposing the bleaching agent with a salt represented by the following general formula (2), without discharging the bath after bleaching, A bleaching dyeing method for fibers, which is characterized by the subsequent dyeing. General formula (1) (However, R is a substituted or unsubstituted alkyl group, an allyl group, or an aralkyl group, and n is a natural number of 1 to 6.) General formula (2) R 1 X (wherein R 1 is a metal ion or substituted or non-substituted) (This represents a substituted quaternary ammonium group, and X represents a halogen ion.)
【請求項2】繊維がセルロース繊維単独またはその他の
繊維と混合したセルロース繊維である第1項記載の繊維
の漂白染色法。
2. The bleaching dyeing method for fibers according to claim 1, wherein the fibers are cellulose fibers alone or mixed with other fibers.
JP25021891A 1991-09-04 1991-09-04 Fiber bleach dyeing method Expired - Fee Related JP3165475B2 (en)

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JP3165475B2 JP3165475B2 (en) 2001-05-14

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000017437A1 (en) * 1998-09-19 2000-03-30 A. Monforts Textilmaschinen Gmbh & Co. Process for preparative and reactive dyeing of cellulose material
CN103541169A (en) * 2013-09-26 2014-01-29 浙江大港印染有限公司 Method for producing computer cross-stitch printed and dyed cloth
CN103981740A (en) * 2014-05-16 2014-08-13 苏州市吴中区大明针织漂染有限公司 Pad dyeing staining method
CN104328615A (en) * 2014-11-19 2015-02-04 南充嘉美印染有限公司 Batik fabric pretreatment device and method
CN108708119A (en) * 2018-06-21 2018-10-26 浙江美欣达纺织印染科技有限公司 Based on the elastic polyurethane fiber cloth production process for evaporating shrinking process

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000017437A1 (en) * 1998-09-19 2000-03-30 A. Monforts Textilmaschinen Gmbh & Co. Process for preparative and reactive dyeing of cellulose material
US6582478B1 (en) 1998-09-19 2003-06-24 A. Monforts Textilmaschinen Gmbh & Co. Process for preparative and reactive dyeing of cellulose material
CN103541169A (en) * 2013-09-26 2014-01-29 浙江大港印染有限公司 Method for producing computer cross-stitch printed and dyed cloth
CN103981740A (en) * 2014-05-16 2014-08-13 苏州市吴中区大明针织漂染有限公司 Pad dyeing staining method
CN104328615A (en) * 2014-11-19 2015-02-04 南充嘉美印染有限公司 Batik fabric pretreatment device and method
CN108708119A (en) * 2018-06-21 2018-10-26 浙江美欣达纺织印染科技有限公司 Based on the elastic polyurethane fiber cloth production process for evaporating shrinking process

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