JPS6269888A - Continuous dyeing method - Google Patents

Continuous dyeing method

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Publication number
JPS6269888A
JPS6269888A JP60210831A JP21083185A JPS6269888A JP S6269888 A JPS6269888 A JP S6269888A JP 60210831 A JP60210831 A JP 60210831A JP 21083185 A JP21083185 A JP 21083185A JP S6269888 A JPS6269888 A JP S6269888A
Authority
JP
Japan
Prior art keywords
dye
group
continuous dyeing
water
dye composition
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
JP60210831A
Other languages
Japanese (ja)
Other versions
JPH048548B2 (en
Inventor
長嶋 進
完二 清水
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 Kasei Corp
Original Assignee
Mitsubishi Kasei 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
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Priority to JP60210831A priority Critical patent/JPS6269888A/en
Publication of JPS6269888A publication Critical patent/JPS6269888A/en
Publication of JPH048548B2 publication Critical patent/JPH048548B2/ja
Granted legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、反応型分散染料の連続染色方法に関する。[Detailed description of the invention] Industrial applications The present invention relates to a continuous dyeing method using reactive disperse dyes.

さらに詳しくは特定の非イオン界面活性剤と有機酸塩を
使用する反応型分散染料の染料組成物を用いた連続染色
方法に関する。
More specifically, the present invention relates to a continuous dyeing method using a dye composition of a reactive disperse dye using a specific nonionic surfactant and an organic acid salt.

従来の技術 従来から、ポリエステル繊維とセルローズ繊維の混紡布
(以下、P / C混紡布と記す)の染色は、ポリエス
テル繊維を分散染料そしてセルローズ繊維を反応染料、
スレン染料、硫化染料などで実施していた。この問題点
として、一種の染料で染色するため色合せが非常に難し
く、又、染色再現性を欠けることが挙げられる。
Conventional Technology Conventionally, blended fabrics of polyester fibers and cellulose fibers (hereinafter referred to as P/C blended fabrics) have been dyed using disperse dyes for polyester fibers, reactive dyes for cellulose fibers,
It was carried out using threne dyes, sulfur dyes, etc. Problems with this include that it is very difficult to match colors because it is dyed with one type of dye, and that dyeing reproducibility is lacking.

新たに、P/C混紡布を反応型分散染料という一つの染
料で染色することが可能になった(第73回繊維加工シ
ンポジウム 昭和!9年/1月り日 繊維学会主催)。
It has now become possible to dye P/C blended fabrics with a single dye called reactive disperse dye (73rd Textile Processing Symposium Showa!9/January 2019, sponsored by the Japan Institute of Textile Science and Technology).

これは、従来の染色において問題となっていた色合せ、
染色再現性を解決するとともに、染料使いを限定するこ
となく種々の実用色で染色することが出来た。
This solves the problem of color matching in conventional dyeing.
In addition to resolving dyeing reproducibility, we were able to dye with a variety of practical colors without limiting the dyes used.

しかしながら、反応型分散染料を用い念連続染色におい
て染着性が劣り、そのために堅牢度及び均染性に問題が
ある。
However, dyeing properties are poor in continuous dyeing using reactive disperse dyes, and therefore there are problems in fastness and level dyeing properties.

上記問題点を改善すべく1本願出願人は、さt!!に、
特定の非イオン界面活性剤及び有機酸塩を使用すること
を特徴とする反応型分散染料の染料組成物に関する発明
を出願した(特願昭1.0−11003号)。
In order to improve the above-mentioned problems, the applicant of this application has decided to solve the following problems: ! To,
He filed an application for an invention relating to a dye composition of a reactive disperse dye characterized by using a specific nonionic surfactant and an organic acid salt (Japanese Patent Application No. 11003/1989).

しかしながら、該染料組成物を用いて、従来の染色工程
によりP/C混紡布の連続染色を行なった場合、セルロ
ーズ繊維への染着性が今一つであり、P / C混紡布
への均染性に問題があった。
However, when continuous dyeing of P/C blend fabrics is carried out using the dye composition in a conventional dyeing process, the dyeability of cellulose fibers is poor, and the level dyeing of P/C blend fabrics is poor. There was a problem.

従来の染色工程例: パッディング   i dlp−t nip  l!Z
’)率6j慢↓ 乾   燥     100℃×l−〇秒↓ 乾熱固着(熱発色工程) ユ10℃X60秒↓ 水   洗 ↓ ↓ 乾   燥    ioo℃XI20秒発明が解決しよ
うとする問題点 本発明は、特定の非イオン界面活性剤及び有機酸塩を使
用することを特徴とする反応型分散染料の染料組成物を
用い、さらに、熱発色工程後にアルカリ処理を施すこと
Kより、P / C混紡布の均染性が良好で、加えて染
着性が高く、提供することを目的とするものである。
Conventional dyeing process example: Padding i dlp-t nip l! Z
') Rate 6j slow ↓ Drying 100℃ x l-〇 seconds ↓ Dry heat fixation (thermal coloring process) Yu 10℃ x 60 seconds ↓ Washing with water ↓ ↓ Drying ioo℃XI 20 seconds Problems to be solved by the present invention uses a dye composition of a reactive disperse dye characterized by the use of a specific nonionic surfactant and an organic acid salt, and further performs an alkali treatment after the thermal coloring process, resulting in a P/C blend. The purpose is to provide cloth with good level dyeing properties and high dyeability.

問題点を解決するための手段′ すなわち、本発明は、水に不溶または難溶性の反応型分
散染料OJ〜30重量%および一般式(Il CM、O(CM、CM、O)、H・曲・〔I〕(式中、
nは6〜30を表わす、)で示される非イオン界面活性
剤コ、!−/、?重量%を含有し、且つ、一般式〔11 (式中、Rは水素原子、炭素数l〜乙の脂肪族基または
芳香族基を表わす。Xは水酸基またはアミノ基を表わす
。MはNH牛、NaまたはKを表わす。aは0〜/、b
はO−コ、Cは0−4を表わす。)で示される有機酸塩
を用いてpH6.5〜7.5に調整された染料組成物を
用いた連続染色において、熱発色工程の後で直ちにアル
カリ処理を施す連続染色方法をその要旨とするものであ
る。
Means for Solving the Problems' That is, the present invention provides 30% by weight of a reactive disperse dye OJ which is insoluble or sparingly soluble in water,・[I] (in the formula,
A nonionic surfactant represented by n represents 6 to 30,! -/、? % by weight, and has the general formula [11 (wherein, R represents a hydrogen atom, an aliphatic group or aromatic group having 1 to 2 carbon atoms, X represents a hydroxyl group or an amino group, and M represents NH , represents Na or K. a is 0 to /, b
represents O-co, and C represents 0-4. ) The gist is a continuous dyeing method in which alkali treatment is immediately applied after the thermal coloring step in continuous dyeing using a dye composition whose pH is adjusted to 6.5 to 7.5 using an organic acid salt shown in It is something.

本発明に使用する水に不溶または難溶性の反応型分散染
料としては、例えば、次の一般式[13で表わされるも
のが挙げられる。
Examples of the water-insoluble or sparingly soluble reactive disperse dye used in the present invention include those represented by the following general formula [13].

(式中、Dは水不溶性の色素残基を表わし、Xは酸素原
子または−NH−基を表わし、YはOR’またはNR’
R’を表わし、RJ、R4およびR1は水素原子または
置換基を有していてもよいアルキル基、アリール基、も
しくはアラルキル基を表わすか、またはR4とHflと
の連結によシ形成されるj員もしくは6員の含窒素複素
環を表わす。)Dとしては、アントラキノン系、アゾ系
、キノフタロン系、メチン系、ヘテロ縮合環系などを挙
げることができる。
(In the formula, D represents a water-insoluble dye residue, X represents an oxygen atom or -NH- group, and Y represents OR' or NR'
R', RJ, R4 and R1 represent a hydrogen atom or an alkyl group, an aryl group, or an aralkyl group which may have a substituent, or are formed by linking R4 and Hfl. represents a nitrogen-containing or 6-membered nitrogen-containing heterocycle. ) Examples of D include anthraquinone systems, azo systems, quinophthalone systems, methine systems, and heterofused ring systems.

本発明の染料組成物中の反応型分散染料の使用量として
はO,S〜30重fk%の範囲を挙げることができ、好
ましくはコ、j〜コQt量俤の範囲を挙げることができ
る。
The amount of the reactive disperse dye used in the dye composition of the present invention can be in the range of O,S to 30 weight fk%, preferably in the range of co,j to coqt amount. .

上記一般式〔I〕で示される非イオン界面活性剤は、た
とえば公知の方法より、メタノールとエチレンオキサイ
ドを付加反応させることによって容易に製造される。
The nonionic surfactant represented by the above general formula [I] can be easily produced by, for example, an addition reaction between methanol and ethylene oxide using a known method.

また、本発明の一般式〔I〕のエチレンオキサイド付加
モル数nは6〜30の範囲で挙げることができ、好まし
くは7〜10の範囲を挙げることができる。更に、その
使用量としてはコ、S〜l!重量%の範囲を挙げること
ができ、好ましくはS、O〜10重量憾重量臼を挙げる
ことができる。
Further, the number n of moles of ethylene oxide added in the general formula [I] of the present invention can be listed in the range of 6 to 30, preferably in the range of 7 to 10. Furthermore, the amount used is ko, S ~ l! A range of weight % can be mentioned, and preferably S, O to 10 weight % can be mentioned.

上記一般式〔]〕で示される有機酸塩は、たとえば次に
挙げられる有機酸のNH4、Naそしてに塩である。
The organic acid salts represented by the above general formula []] are, for example, NH4, Na, and salts of the following organic acids.

ギ    酸     HCOOH 酢   酸     CH,COO1’I安息香酸  
 C6H,C0OH フタル酸   C6H4(Coo)I)。
Formic acid HCOOH Acetic acid CH,COO1'Ibenzoic acid
C6H,C0OH Phthalic acid C6H4(Coo)I).

乳   酸     CFI、CH(OH)COOHシ
ュウ酸   (COOfl)。
Lactic acid CFI, CH(OH)COOH oxalic acid (COOfl).

コハク酸   (CH,C00H)を 酒石酸  HO−CfI−Coo)f ■ HO−CH−Coo)I CH,−COOH カルバミン酸   H,NC00H (通常、アンモニウム塩として存在する)また、本発明
の一般式〔■〕でのpH調整は6、S〜7.5の範囲が
挙げられる。好ましくはす、t〜7.−を挙げることが
できる。
Succinic acid (CH,C00H) is converted into tartaric acid HO-CfI-Coo)f ■ HO-CH-Coo)I CH,-COOH Carbamic acid H,NC00H (usually present as an ammonium salt) Also, the general formula of the present invention [ The pH adjustment in [2] is within the range of 6.S to 7.5. Preferably, t~7. − can be mentioned.

本発明の染料組成物は、上記反応型分散染料と一般式〔
I〕の非イオン界面活性剤および一般式[11〕の有機
酸塩とを水中に分散/溶解させることによシ得られる。
The dye composition of the present invention comprises the above reactive disperse dye and the general formula [
It can be obtained by dispersing/dissolving the nonionic surfactant of formula [I] and the organic acid salt of general formula [11] in water.

さらに、本発明の染料組成物は、上記分散染料と一般式
〔I〕で示される非イオン界面活性剤および一般式〔■
〕で表わされる有機酸塩とを水に分散/溶解することに
よって得られるが、上記水の使用量としては50重量−
以上、好ましくは70〜95重量慢の範囲を挙げること
ができる。
Furthermore, the dye composition of the present invention comprises the above-mentioned disperse dye, a nonionic surfactant represented by the general formula [I], and a general formula [■
] is obtained by dispersing/dissolving in water, the amount of water used is 50% by weight.
As mentioned above, the preferred range is 70 to 95 weight.

また、本発明の染料組成物はlj重量優以下の浸透・湿
潤剤、ヒドロトロープ剤、マイグレーション防止剤など
を添加しても差支えない。
Further, the dye composition of the present invention may contain a penetrating/wetting agent, a hydrotrope agent, a migration inhibitor, etc. in an amount of not more than lj weight.

浸透・湿潤剤としては、ダイアサーバーPN−8R(三
菱化成工業株式会社製造、商標)、サクシツールC8(
日本染化工業株式会社製造、商標)、テキスボー)D−
21I(日華化学工業株式会社製造、商標)などが挙げ
られる。
As penetrating/wetting agents, Diaserver PN-8R (manufactured by Mitsubishi Chemical Industries, Ltd., trademark), Sakushitool C8 (
Manufactured by Nippon Someka Kogyo Co., Ltd. (Trademark), Textbook) D-
21I (manufactured by NICCA CHEMICAL INDUSTRY CO., LTD., trademark) and the like.

ヒドロトロープ剤としては、尿素、ジメチル尿素、トル
エンスルホン散ンーダなどが挙げられる。
Examples of hydrotropes include urea, dimethylurea, and toluene sulfone duster.

マイグレーション防止剤としては、ダイアサーバーMG
−N(三菱化成工業株式会社製造、商標)、タマノIJ
sA−コj(荒川化学工業株式会社製造、商標)、ミグ
ノンNS(日本染化工業株式会社製造、商標)、ダック
アルギンNSPM(株式会社紀文製造、商標)などが挙
げられる。
As a migration prevention agent, Diaserver MG
-N (manufactured by Mitsubishi Chemical Industries, Ltd., trademark), Tamano IJ
Examples include sA-Coj (manufactured by Arakawa Chemical Industry Co., Ltd., trademark), Mignon NS (manufactured by Nippon Someka Kogyo Co., Ltd., trademark), and Duck Algin NSPM (trademark, manufactured by Kibun Manufacturing Co., Ltd.).

本発明の連続染色方法は、ポリエステル繊維とセルロー
ズ繊維との混紡率が65’対35重量饅である布の場合
、上述染料組成物を用いて。
The continuous dyeing method of the present invention uses the above-mentioned dye composition in the case of fabric in which the blend ratio of polyester fiber and cellulose fiber is 65:35 by weight.

内の染色工程を取ることを特徴としている。It is characterized by a dyeing process within the dyeing process.

染色工程: パッド浴調製    染料組成物 ↓ パッディング    / dip−/ nip絞シ率6
!係↓ 乾   燥      /θθCX/−〇秒↓ 乾熱固着    コ1ocXbo秒 ↓ ↓ 乾   燥 更に、本発明の連続染色でのアルカリ処理において、ア
ルカリ剤としては水酸化ナトリウム、水酸化カリウム、
炭酸ナトリウム、重炭酸ナトリウム、ケイ酸ナトリウム
などの無機アルカリが挙げられ、好ましくは水酸化ナト
リウム、ケイ酸ナトリウムが挙げられる。これらアルカ
リ剤の使用濃度はO,コ〜ユ重itチ水溶液の範囲で使
用するが、好ましくはo、s −i、s重1に%水溶液
の範囲を挙げることができる。
Dyeing process: Pad bath preparation Dye composition ↓ Padding / dip- / nip squeeze rate 6
! ↓ Drying / θθCX / -0 seconds ↓ Dry heat fixation
Examples include inorganic alkalis such as sodium carbonate, sodium bicarbonate, and sodium silicate, with sodium hydroxide and sodium silicate being preferred. The concentration of these alkaline agents used is in the range of 0.5% to 1% aqueous solution, preferably 1% aqueous solution.

又、アルカリ処理条件は、次のものが好ましい。Further, the following conditions for the alkali treatment are preferable.

Oアルカリパッド →スチーミング 100−110℃
Oアルカリパッド→ベーキング  /317〜コJoc
Oアルカリ熱水          6o〜1ooc実
施例 次に本発明を実施例により更に具体的に説明するが本発
明は以下の実施例に限定されるものではない。
O alkaline pad → steaming 100-110℃
O alkaline pad → baking /317~ko Joc
EXAMPLES Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to the following Examples.

なお、実施例および比較例における反応型分散染料の調
製と連続染色方法および各種評価方法は以下の通りであ
る。
The preparation of reactive disperse dyes, continuous dyeing methods, and various evaluation methods in Examples and Comparative Examples are as follows.

(1)  反応型分散染料の調製 下記組成 反応型分散染料       lj? 〔下記構造式(イ)、(ロ)又はP−) )リグニンス
ルホン酸塩     3? (Wsatvaeo社製、商標R@axg、を人)エチ
レングリコール      S? 水                    り3 ?
計            l θθ?の混合物を室温
下、サンドグラインダー中で粉砕し染料分散液を調製し
た。
(1) Preparation of reactive disperse dye Reactive disperse dye lj? [Structural formula (a), (b) or P-) below] Lignosulfonate 3? (Manufactured by Wsatvaeo, trademark R@axg) Ethylene glycol S? Water 3?
Total l θθ? The mixture was ground in a sand grinder at room temperature to prepare a dye dispersion.

赤色 青  色 紺  色             ・・・・・・(ハ
)(2)連続染色方法 所定の染料組成物を調製しパッド浴とする。
Red Blue Navy Blue Color (c) (2) Continuous Dyeing Method A prescribed dye composition is prepared and used as a pad bath.

これを用いてポリニスデル繊維とセルローズ繊維との混
紡率が6S対35重量%である布を連続染色する。その
工程と条件は次の通りである。
This is used to continuously dye a cloth in which the blend ratio of polynisder fibers and cellulose fibers is 6S to 35% by weight. The process and conditions are as follows.

(21−a  実施例の場合(本発明の染色工程)パッ
ディング   / dlp  / nip絞シ率i、s
%↓ 乾   燥     ioo℃X/コO秒↓ 乾熱固着   コ1OcX6θ秒 ↓ 乾   燥     toocxtコO秒(2)$ b
  比較例の場合(従来の染色工程)パッティング  
 / dlp  / nip絞り率l]↓ 乾   燥     too℃Xt2oyyf)↓ 乾熱固着   コl0CXAO秒 ↓ 水   洗 ↓ 洗   浄    炭鍍ソーダコ?/1、ダイアサーノ
(−8C−CTTa2コ?/L ↓     tO℃XIO分 水   洗 乾   燥     1oocXiコ0秒(3)  染
着性評価 前記(1)で得られた染色布の表面反射率を色差計(日
本電色工業株式会社製造)により測定し、比較例で得ら
れた染色布の表面反射率を100(標準)として相対的
な数値を算出した。
(21-a In the case of Example (dying process of the present invention) Padding / dlp / nip squeeze rate i, s
%↓ Drying ioo℃X/kooseconds↓ Dry heat fixation ko1ocx6θseconds↓ Drying tooocxtkooseconds (2) $ b
In the case of comparative example (conventional dyeing process) putting
/ dlp / nip squeezing rate l]↓ Drying too℃ /1, Diasano (-8C-CTTa2?/L ↓ tO℃XIO Water separation Washing Drying 1oocXi 0 seconds (3) Dyeability evaluation Measure the surface reflectance of the dyed cloth obtained in (1) above using a color difference meter. (manufactured by Nippon Denshoku Kogyo Co., Ltd.), and a relative value was calculated by setting the surface reflectance of the dyed cloth obtained in the comparative example as 100 (standard).

(4)堅牢度評価 (亀)  耐  光 JIS規格のLOざ1I2−197/に準じ、l/lN
濃度の染色布を用いて、カーボンアーク下で20および
lIo時間照射後の退色を評価した。
(4) Fastness evaluation (tortoise) Light resistance According to JIS standard LOza 1I2-197/1/1N
Color fading was evaluated after irradiation for 20 and 10 hours under a carbon arc using dyed fabrics of 100% density.

(b)摩擦 JIB規格のLOg IIタデ−971に準じ、1Zl
No度の染色布を用いて、toos含水木綿布への摩擦
汚染を単振型摩擦試験機にて評価した。
(b) According to Friction JIB standard LOg II Tade-971, 1Zl
Frictional contamination of too water-containing cotton cloth was evaluated using a single vibration type friction tester using dyed cloth of No.

(51均染性評価 /// N濃度の染色布を用いて、染色均一性(スジ斑
など)を比較例で得られた染色布と相対比較し評価した
(51 Evaluation of uniformity of dyeing /// Using a dyed fabric with N concentration, the dyeing uniformity (streak spots, etc.) was evaluated by relative comparison with the dyed fabric obtained in the comparative example.

○    Δ−−→× 優れる  均染性 劣る 実施例1 下記組成 染料分散液〔(イ)〕!? CI’l、04 CH,CH,OテHS?浸透剤〔ダイ
アサーバーPN−8R)        0.lfマイ
グレーション防止剤[ダイアサーバーMG−N]0./
%尿   素                   
   /?C6H5COON m水溶液       
    pH71S11!整水          残
量 計                 100fから成
る染料組成物を用いて、前[(2) −aの連続染色を
実施した。その結果、非常に染着性(濃色性)に富んだ
均一赤色染色布を得ることが出来た。
○ Δ−−→× Excellent Level dyeing performance Poor Example 1 Dye dispersion with the following composition [(a)]! ? CI'l, 04 CH, CH, OteHS? Penetrant [Diaserver PN-8R] 0. lf migration inhibitor [Diaserver MG-N] 0. /
% urea
/? C6H5COON m aqueous solution
pH71S11! Continuous dyeing of (2)-a was performed using a dye composition consisting of 100f. As a result, it was possible to obtain a uniformly red dyed cloth with extremely high dyeability (deep color).

染着性、堅牢度、均染性についての結果は従来の結果と
比較して第1表に示す。
The results regarding dyeing properties, fastness, and leveling properties are shown in Table 1 in comparison with conventional results.

実施例コ 下記組成 染料分散液〔(ロ)〕!? CH,O+CH,CH,O%Hf p 浸透剤〔ダイアサーバーPN−8R)        
0.lfマイグレーション防止剤[ダイアサーバーMG
−N]0./%尿   累             
         l?CH1COONH,水溶液  
          pH7調整水         
 残量 計                 100f−から
成る染料組成物を用いて、前記12)−aの連続染色を
実施した。その結果、著しく染着性(濃色性)の良好で
青色=均染な染色布を得ることが出来た。
Example Dye dispersion with the following composition [(b)]! ? CH, O+CH, CH, O%Hf p Penetrant [Diaserver PN-8R]
0. lf migration inhibitor [Diaserver MG
-N]0. /% urine cumulative
l? CH1COONH, aqueous solution
pH7 adjusted water
Continuous dyeing in 12)-a above was carried out using a dye composition consisting of 100f-. As a result, it was possible to obtain a dyed cloth with extremely good dyeability (deep color) and even blue dyeing.

結果を第1表に示す。The results are shown in Table 1.

実施例3 下記組成 染料分散液〔ヒう〕         コO?CH1O
÷CH,CM、O輻H10f 浸透剤〔ダイアサーバーPN−8RI        
O,/ fマイグレーション防止剤〔ダイアサーバーM
G−N]0.ip尿   累            
          l?CH1−COONM。
Example 3 Dye dispersion liquid with the following composition. CH1O
÷CH, CM, O radiance H10f Penetrant [Diaserver PN-8RI
O,/f Migration inhibitor [Diaserver M
G-N]0. IP urine accumulation
l? CH1-COONM.

HO−C−COONH,水浴液        pH7
調整CH,−COONH。
HO-C-COONH, water bath solution pH 7
Adjustment CH, -COONH.

水                        
残 置針                 1oo1
から成る染料組成物を用いて、前記(21−aの連続染
色を実施した。その結果、染着性に優れ、良好な均染性
の紺色布を得ることが出来た。
water
Remaining needle 1oo1
Continuous dyeing of the above (21-a) was carried out using the dye composition consisting of (21-a). As a result, a dark blue cloth with excellent dyeing properties and good level dyeing properties was obtained.

結果を比較例とともに第1表に示す。The results are shown in Table 1 along with comparative examples.

比較例1 実施例1で用いた染料組成物で前記t2+−bの連続染
色を実施したところ実施例1に比較し、均染性、染着性
等が劣る赤色染色布が得られた。
Comparative Example 1 When continuous dyeing of t2+-b was carried out using the dye composition used in Example 1, a red dyed cloth was obtained which was inferior in level dyeing properties, dyeability, etc. as compared to Example 1.

結果を第1表に示す。The results are shown in Table 1.

比較例コ 実施例コで用いた染料組成物で前記+21−bの連続染
色を実施したところ実施例コに比較し均染性、染着性等
が劣る青色染色布が得られた。
Comparative Example When continuous dyeing of +21-b was carried out using the dye composition used in Example C, a blue dyed fabric was obtained which was inferior in level dyeing properties, dyeability, etc. as compared to Example Co.

結果を第1表に示す。The results are shown in Table 1.

比較例3 実施例3で用いた染料組成物で前記+2)−bの連続染
色を実施したところ実施例3に比較し均染性、染漫性婢
が劣る紺色染色布を得た。
Comparative Example 3 When the dye composition used in Example 3 was used to carry out the continuous dyeing of +2)-b, a dark blue dyed cloth was obtained which was inferior in level dyeing properties and dyeing properties compared to Example 3.

結果を第1表に示す。The results are shown in Table 1.

比較例ダ 下記組成 染料分散液〔(ハ)〕         コ0?CH,
O+(HHHOH10+T?lH/  0  ≦1浸透
剤〔ダイアサーバーPN−8R)        0.
lfマイグレーション防止剤〔ダイアサーバーMG−N
]o、ty尿    素              
         l?水             
          残 置針           
      1ooyから成る染料組成物を用いて、前
記+2+−mの連続染色を実施したところ実施例3に比
較し均染性、染着性等が劣る紺色染色布を得た。
Comparative Example: Dye dispersion with the following composition [(c)] 0? CH,
O+(HHHOH10+T?lH/0 ≦1 Penetrant [Diaserver PN-8R) 0.
lf migration inhibitor [Diaserver MG-N
] o, ty urea
l? water
Remaining needle
When continuous dyeing of +2+-m was carried out using the dye composition consisting of 1oooy, a dark blue dyed cloth was obtained which was inferior in level dyeing properties, dyeability, etc. as compared to Example 3.

結果を第1表に示す。The results are shown in Table 1.

比較例! 下記組成 染料分散液〔(ハ)〕         コ01浸透剤
〔ダイアサーバーPN−sR〕       θ、/ 
pマイグレーション防止剤〔ダイアサーバーMG−N〕
  θ、11尿   素              
        720M、−COONH4 HO−C−COONH4水溶液 CH2−COONH4、H7調整 水          残量 引        / 00f から成る染料組成物を用いて、前記+2)−aの連続染
色を実施したところ実施例3に比較し均染性及び染着性
が著しく劣る紺色染色布を得た。
Comparative example! Dye dispersion liquid with the following composition [(c)] Co01 Penetrant [Diaserver PN-sR] θ, /
p migration inhibitor [Diaserver MG-N]
θ, 11 urea
720M, -COONH4 HO-C-COONH4 aqueous solution CH2-COONH4, H7 adjusted water Remaining amount subtracted / 00f When the continuous dyeing of the above +2)-a was carried out, it was more even than in Example 3. A dark blue dyed fabric with significantly poor dyeability and dyeability was obtained.

結果を第1表に示す。The results are shown in Table 1.

比較例6 下記組成 染料分散液〔(ハ)〕         −〇?cH3
o+cH,cH,o+THt o y浸透剤〔ダイアサ
ーバーPN  SRI        O,/ y−マ
イグレーション防止剤〔ダイアサーバーMG−N]0.
/7尿    素                 
      l?C)lニーC00NEI。
Comparative Example 6 Dye dispersion liquid with the following composition [(c)] −〇? cH3
o+cH,cH,o+THto y Penetrant [Diaserver PN SRI O,/y-Migration inhibitor [Diaserver MG-N]0.
/7 urea
l? C)lnee C00NEI.

から成る染料組成物を用いて、前記+21−aの連続染
色を実施したところ実施例3に比較し均染性、染着性等
が劣る紹色染色布を得た。
When continuous dyeing of +21-a was carried out using the dye composition consisting of the dye composition, a halo-dyed cloth with inferior level dyeing properties, dyeability, etc., as compared to Example 3 was obtained.

結果を第7表に示す。The results are shown in Table 7.

Claims (3)

【特許請求の範囲】[Claims] (1)水に不溶または難溶性の反応型分散染料0.5〜
30重量%および一般式〔 I 〕 CH_3O(CH_2CH_2O)_nH・・・・・・
〔 I 〕(式中、nは6〜30を表わす)で示される非
イオン界面活性剤2.5〜15重量%を含有し、且つ、
一般式〔II〕 ▲数式、化学式、表等があります▼・・・・・・〔II〕 (式中、Rは水素原子、炭素数1〜6の脂肪族基または
芳香族基を表わし、Xは水酸基またはアミノ基を表わし
、MはNH_4、K、またはNaを表わし、そしてaは
0〜1、bは0〜2、cは0〜2を表わす)で示される
有機酸塩を用いてpH6.5〜7.5に調整された染料
組成物を用いた連続染色において、熱発色工程の後で直
ちにアルカリ処理を施すことを特徴とする連続染色方法
(1) Reactive disperse dye that is insoluble or poorly soluble in water 0.5~
30% by weight and general formula [I] CH_3O(CH_2CH_2O)_nH...
[I] (in the formula, n represents 6 to 30) containing 2.5 to 15% by weight of a nonionic surfactant, and
General formula [II] ▲ Numerical formulas, chemical formulas, tables, etc. are available▼・・・・・・[II] (In the formula, R represents a hydrogen atom, an aliphatic group having 1 to 6 carbon atoms, or an aromatic group, represents a hydroxyl group or an amino group, M represents NH_4, K, or Na, and a represents 0 to 1, b represents 0 to 2, and c represents 0 to 2). A continuous dyeing method using a dye composition adjusted to a dye composition having a dye composition of .
(2)特許請求の範囲第1項記載の連続染色方法におい
て、水に不溶または難溶性の反応型分散染料が、一般式
〔III〕で表わされる方法。 ▲数式、化学式、表等があります▼・・・・・・〔III
〕 (式中、Dは水不溶性の色素残基を表わし、Xは酸素原
子または−NH−基を表わし、YはOR^3またはNR
^4R^5を表わし、R^3、R^4およびR^3は水
素原子または置換基を有していてもよいアルキル基、ア
リール基、もしくはアラルキル基を表わすか、またはR
^4とR^5との連結により形成される5員もしくは6
員の含窒素複素環を表わす)
(2) The continuous dyeing method according to claim 1, wherein the reactive disperse dye that is insoluble or poorly soluble in water is represented by the general formula [III]. ▲There are mathematical formulas, chemical formulas, tables, etc.▼・・・・・・[III
] (In the formula, D represents a water-insoluble dye residue, X represents an oxygen atom or -NH- group, and Y represents OR^3 or NR
^4R^5 represents R^3, R^4 and R^3 represent a hydrogen atom or an alkyl group, aryl group, or aralkyl group which may have a substituent, or R
5-membered or 6-membered by connecting ^4 and R^5
(represents a nitrogen-containing heterocycle)
(3)特許請求の範囲第1項記載の連続染色方法におい
て、アルカリ処理が、水酸化ナトリウム、水酸化カリウ
ム、炭酸ナトリウム、重炭酸ナトリウム、ケイ酸ナトリ
ウムなど無機アルカリの0.2〜2重量%水溶液を発色
布に含浸させたのち、熱処理を施す方法。
(3) In the continuous dyeing method according to claim 1, the alkali treatment is performed in an amount of 0.2 to 2% by weight of an inorganic alkali such as sodium hydroxide, potassium hydroxide, sodium carbonate, sodium bicarbonate, or sodium silicate. A method in which colored cloth is impregnated with an aqueous solution and then heat treated.
JP60210831A 1985-09-24 1985-09-24 Continuous dyeing method Granted JPS6269888A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60210831A JPS6269888A (en) 1985-09-24 1985-09-24 Continuous dyeing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60210831A JPS6269888A (en) 1985-09-24 1985-09-24 Continuous dyeing method

Publications (2)

Publication Number Publication Date
JPS6269888A true JPS6269888A (en) 1987-03-31
JPH048548B2 JPH048548B2 (en) 1992-02-17

Family

ID=16595834

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60210831A Granted JPS6269888A (en) 1985-09-24 1985-09-24 Continuous dyeing method

Country Status (1)

Country Link
JP (1) JPS6269888A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011201552A (en) * 2010-03-24 2011-10-13 Nippon Jido Seiki Kk Cartoner

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6039795A (en) * 1983-08-13 1985-03-01 松下電工株式会社 Device for starting discharge lamp

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6039795A (en) * 1983-08-13 1985-03-01 松下電工株式会社 Device for starting discharge lamp

Also Published As

Publication number Publication date
JPH048548B2 (en) 1992-02-17

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