JPH0465586A - Dyeing of conjugate structure - Google Patents

Dyeing of conjugate structure

Info

Publication number
JPH0465586A
JPH0465586A JP2176792A JP17679290A JPH0465586A JP H0465586 A JPH0465586 A JP H0465586A JP 2176792 A JP2176792 A JP 2176792A JP 17679290 A JP17679290 A JP 17679290A JP H0465586 A JPH0465586 A JP H0465586A
Authority
JP
Japan
Prior art keywords
dyeing
dye
bath
polyamide
polyester
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2176792A
Other languages
Japanese (ja)
Inventor
Shunei Takeda
武田 俊英
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.)
Kanebo Ltd
Original Assignee
Kanebo 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 Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP2176792A priority Critical patent/JPH0465586A/en
Publication of JPH0465586A publication Critical patent/JPH0465586A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the title dyed material having uniformity and excellent fastness, by dyeing a conjugate yarn structure containing polyester-based yarn and polyamide-based yarn in the dyeing bath using both disperse dye and specific dye to stand reducing cleaning by one-bath dyeing and reducing and cleaning under an acidic condition. CONSTITUTION:In dyeing a conjugate yarn structure comprising polyester-based yarn and polyamide-based yarn, the structure is dyed in a dyeing solution in the same bath using both disperse dye and dye having >=70% durability of reducing cleaning and containing sodium sulfonate group in the structure of dye by one-bath dyeing, reduced and cleaned under an acidic condition to give a high-quality dyed material having excellent fastness of dyeing uniformly by one bath.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、ポリエステル系繊維とポリアミド系繊維の両
者を用いた複合繊維構造物の染色方法に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for dyeing a composite fiber structure using both polyester fibers and polyamide fibers.

(従来の技術) 近年、ポリエステル成分とポリアミド成分とを接合した
分割型複合繊維等が多方面に用いられるようになったた
め、染色性を異にした一11az・らなる複合繊維構造
物を高品位、高能率に染色することが求められている。
(Prior art) In recent years, splittable conjugate fibers made by joining polyester components and polyamide components have come to be used in many fields. , there is a need for highly efficient dyeing.

従来、このような繊維構造物の染色法としては、濃色の
場合は先ずポリエステルを分散染料で真正染色し、ハイ
ドロサルファイド等の還元剤、アルカリ金属塩、界面活
性剤を含む水溶液で処理後、ポリアミドを酸性染料、酸
性金属錯塩染料、直接染料等のポリアミドに親和性のあ
る染料で染色後フィックス処理やソーピング処理を行な
う二浴染色法が最も一般的である。ただし、二浴染色法
は工程が11雑となり効率が低下するため、これを−浴
にて行うことが試みられている。
Conventionally, the dyeing method for such fiber structures has been to first dye polyester with a disperse dye in the case of a deep color, then treat it with an aqueous solution containing a reducing agent such as hydrosulfide, an alkali metal salt, and a surfactant. The most common method is a two-bath dyeing method in which polyamide is dyed with a dye that has an affinity for polyamide, such as an acid dye, an acidic metal complex dye, or a direct dye, followed by a fixing treatment or soaping treatment. However, since the two-bath dyeing method involves 11 complicated steps and reduces efficiency, attempts have been made to carry out this process in a bath.

例えば、特開昭82,2311887号公報には、ポリ
アミド及びポリエステルを含有する繊維構造物を分散染
料を用いてポリエステルの条件で染色し、ナイロンのゼ
イ化をタンニン酸処理により抑制する方法が記載されて
いる。
For example, JP-A No. 82,2311887 describes a method in which a fiber structure containing polyamide and polyester is dyed under polyester conditions using a disperse dye, and zeification of nylon is suppressed by treatment with tannic acid. ing.

又、ぼりエステルに染着性のある分散染料とポリアミド
に染着性を示す酸性染料、酸性金属錯塩染料、直接染料
等その構造中にスルホン酸ソーダ基を持つ染料を併用し
ポリエステルとポリアミドを同時に染色する方法も知ら
れている。
In addition, we can simultaneously dye polyester and polyamide by using a combination of disperse dyes that dye esters and dyes that have sodium sulfonate groups in their structures, such as acid dyes, acidic metal complex dyes, and direct dyes that dye polyamides. Methods of dyeing are also known.

更に、最近では分散型反応染料でポリエステルとポリア
ミドを同時に一浴で染色する方法も考案されている。
Furthermore, a method has recently been devised in which polyester and polyamide are dyed simultaneously in one bath using a dispersed reactive dye.

(発明が解決しようとするRH) しかしながら、前述の従来技術では、分散染料を還元洗
浄することが必須であり、還元洗浄を行うとポリアミド
に汚染した分散染料が除去されるでけではなく、せっか
くポリアミドに染着した構造中にスルホン酸ソーダ基を
持つ染料も同時に脱落させてしまい、目的が達せられず
、結果的にポリエステルのみが染色されポリアミドが白
残しに近い状態になる。又、これを避けるためには染料
を分解除去する還元洗浄の代りに染料を分解せずZζ除
去する活性剤を用いたソーピング法が採られる。この方
法では淡色の場合は良いが、中濃色の場合は製品の染色
堅牢度に間#Ijp # スる。又、分割型極細複合繊
組の染色に実施する場合、活性剤だけでのソーピングで
はボリア之ド繊維へ汚染した不安定な染料を十分に除去
することかや実上不可能である。
(RH to be solved by the invention) However, in the above-mentioned conventional technology, it is essential to perform reduction cleaning of the disperse dye, and when performing reduction cleaning, the disperse dye that has contaminated the polyamide is not only removed; The dye having a sodium sulfonate group in the dyed structure of the polyamide is also removed at the same time, and the purpose is not achieved.As a result, only the polyester is dyed, leaving the polyamide almost white. In order to avoid this, a soaping method using an activator that removes Zζ without decomposing the dye is used instead of reduction washing that decomposes and removes the dye. This method works well for light colors, but for medium to dark colors, the color fastness of the product will be affected. Furthermore, when dyeing split-type ultrafine composite fibers, soaping with only an activator may not be able to sufficiently remove unstable dyes that have contaminated the boria fibers.

本発明は、かかる間聞点を解決するものであって、分散
染料と酸性染料等による二浴浸漬染色1去と同等の色相
と#度、及び染色堅牢!を与え、且つ生産性の高いポリ
エステルとポリアミドから、I″る適合合成am構造物
、就中分#I型極@a維からなる繊維構造物に好適な染
色法の提供を目的とするものである。
The present invention solves this problem, and provides the same hue and degree of dyeing as two-bath immersion dyeing using disperse dyes and acid dyes, and dyeing fastness! The purpose of the present invention is to provide a dyeing method suitable for synthetic am structures made of polyester and polyamide with high productivity, and particularly for fiber structures made of #I type polar @a fibers. be.

C問題点を解決するための手段) 本発明は、ポリエステル系繊維とポリアミド系a維とを
含む複合ia櫂臂造物を染色するに於いて、分散染料と
還元洗浄耐久性が7096以上のスルホン酸ソーダ基を
構造中に持つ染料とを併用して同浴染色し、その後酸性
条件下で還元洗浄することを特徴とするものである。
Means for Solving Problem C) The present invention uses a disperse dye and a sulfonic acid having a reduction washing durability of 7096 or higher in dyeing a composite IA structure containing polyester fibers and polyamide A fibers. It is characterized by dyeing in the same bath using a dye having a soda group in its structure, followed by reduction washing under acidic conditions.

本発明のポリアミドとしては、例えばナイロン4、ナイ
ロン8、ナイロン1、ナイロン11、ナイロン12、ナ
イロン61B、ナイロンg、to、ポリメタキシレンア
ジパミド、ポリバラキシリレンデカンアミド、ポリビス
シクロヘキシルメタンデカンアミド及びこれらを成分と
するコポリアミド等が挙げられる。
Examples of the polyamide of the present invention include nylon 4, nylon 8, nylon 1, nylon 11, nylon 12, nylon 61B, nylon g, to, polymethaxylene adipamide, polyvaraxylylene decanamide, polybiscyclohexylmethanedecaneamide. and copolyamides containing these as components.

一方、ポリエステルとしては、例えばプリエチレンテレ
フタレート、ポリテトラメチレンテレフタレート、ポリ
エチレンオキシベンゾエート、ポリ1,4−ジメチルシ
クロヘキサンテレフタレート、ポリピバロラクトン及び
これらを成分とするコポリエステル等がある。
On the other hand, examples of polyesters include polyethylene terephthalate, polytetramethylene terephthalate, polyethyleneoxybenzoate, poly1,4-dimethylcyclohexane terephthalate, polypivalolactone, and copolyesters containing these as components.

本′J@明で云う繊維構造物とは、前記の如きポリアミ
ド及びポ“ノエステルを含有する賜物・織物・不鷹布で
あればよく、特に後述の複合!I維を用いた場合、立毛
品となすとよい。又、ポリアミドは繊維構造物重量に対
し、51量喬以上となれば染色性の斑が生じるため本発
明方法が有効となり、高々5G!量−程度までは斑の発
生が大きい。ポリアミド及びポリエステルの使用方法と
しては交編、交織、混紡等の他、両成分よりなる複合!
l維を用いて編織する方法が挙げられるが、特に複合繊
維を用いた繊維構造物は本発明方法の効果が大きい。か
かる複合繊、雄としては、分割後の単糸1度が1デニー
ル以下程實となるもので、ポリアミド成分とポリエステ
ル成分が単一フィラメントの任富膚斯面において、一方
の成分を他方の成分が完全に包囲することなく両成分が
接合された形状を有する複合繊維、具体的には横断面が
サイドバイサイド型の複合aim、サイドバイサイド繰
返し型の複合ia維、サイドバイサイドを繰返し中空部
分を形成する複合繊維等が挙げられ、この他に放射型の
形状を有する成分と該放射部を補完する形状を有する池
の成分からなる複合繊維等を挙げることができる。
The fiber structure referred to in this book'J@mei may be any fabric, fabric, or nonwoven fabric containing polyamide and polyester as described above, and especially when using the composite I fiber described later, it may be a napped product. In addition, if the amount of polyamide is 51% or more relative to the weight of the fiber structure, staining spots will occur, so the method of the present invention will be effective, and if the amount is at most 5G!, the occurrence of spots will be large. .Polyamide and polyester can be used in combinations such as mixed knitting, mixed weaving, blended spinning, etc., as well as composites made of both components!
Examples include a method of knitting and weaving using conjugate fibers, but the method of the present invention is particularly effective for fiber structures using composite fibers. Such composite fibers are those in which each single fiber after splitting is less than 1 denier, and in which the polyamide component and the polyester component are a single filament, one component is combined with the other component. Composite fibers that have a shape in which both components are joined without completely enclosing them, specifically composite fibers with a side-by-side type cross section, composite IA fibers with a side-by-side repeating type, and composite fibers with a side-by-side repeating type forming a hollow part. Other examples include composite fibers consisting of a component having a radial shape and a pond component having a shape that complements the radiant portion.

次に、還元洗浄耐久性が70%以上のスルホン酸ソーダ
基を構造中に持つ染料(以下単Iζ染料と云うことがあ
る)は、これを用いて分散染料の染色条件(例えば15
0°Cで1時間)で染色してに/S値を測定し、次いで
pHsに調整した還元洗浄液(例えばソジウムホルムア
ルデヒドJで還元洗浄を行ない(例えば90℃で20分
I′tl)、K/S値を測定することにより次式の如く
還元洗浄耐久性を求めることができるつ かかる染料としては例えば、 Ac1d Red 97 Acid Brown 127 Acid Yellow 127 Direct Yellow 2 g Direct Blue 10 g Acid Black 155 ム1zen 8pion Red 2 W      
(保土谷化学製)ム1zenムn1lon dark 
Blue TRL ()の鮮から選ばれた染料が使用で
きるが、還元洗浄耐久性さえ得られれば勿論これに限定
されるものではない。
Next, a dye having a sodium sulfonate group in its structure that has a reduction washing durability of 70% or more (hereinafter sometimes referred to as a single Iζ dye) can be used under the dyeing conditions of a disperse dye (for example, 15
0°C for 1 hour) to measure the /S value, and then perform reduction washing with a reducing washing solution (e.g. sodium formaldehyde J (e.g. 90°C for 20 min I'tl) adjusted to pHs), K Examples of dyes whose reduction cleaning durability can be determined by measuring the /S value are as follows: Acid Red 97 Acid Brown 127 Acid Yellow 127 Direct Yellow 2 g Direct Blue 10 g Acid Black 155 Mu 1zen 8pion Red 2 W
(Manufactured by Hodogaya Chemical) Mu1zenmu n1lon dark
A dye selected from Blue TRL () can be used, but it is of course not limited thereto as long as it has resistance to reduction washing.

本発明では前記の染料と分散染料とを同浴で用いて染色
する。かかる際には、分散均染剤、pH調整剤等を併用
することが好ましい。又、染色は分散染料の染色条件を
用いればよいがポリアミドamのゼイ化を防止するため
110〜130’Cで30〜90分、1!程!高圧染色
を行なうことが好ましい。染色後はポリアミドIa1/
IAの色相の還元洗浄耐久性を向上させるため、0.6
〜15重量嘩、好ましくは2〜6重量囁のタンニン酸を
溶解した水溶液で処理することが好ましい。タンニン酸
は151量優より大きくなると効果は飽和し、更に本処
理後、繊維構造物にタンニン酸の粉状物が付着するため
好ましくない。かかる処理は、タンニン酸水溶液中に繊
、ism造物を浸漬する方法が好ましく、水溶液温度と
しては常温〜100℃、特に70〜90℃が好ましい。
In the present invention, the above-mentioned dye and disperse dye are used in the same bath for dyeing. In such a case, it is preferable to use a dispersion leveling agent, a pH adjuster, etc. in combination. Also, dyeing can be done using disperse dye dyeing conditions, but in order to prevent the polyamide am from turning into a zeitge, at 110 to 130'C for 30 to 90 minutes, 1! Mode! Preferably, high-pressure staining is performed. After dyeing, polyamide Ia1/
0.6 to improve the reduction cleaning durability of the IA hue.
Preferably, the treatment is carried out with an aqueous solution containing 15 to 15% by weight of tannic acid, preferably 2 to 6% by weight. If the amount of tannic acid is greater than 151, the effect will be saturated, and tannic acid powder will adhere to the fiber structure after this treatment, which is not preferable. Such treatment is preferably carried out by immersing the fibers or ism products in an aqueous tannic acid solution, and the temperature of the aqueous solution is preferably room temperature to 100°C, particularly 70 to 90°C.

又、他の処理方法例えばプリント或いはスプレーする方
法も有効である。
Other processing methods such as printing or spraying are also effective.

次に、還元洗浄を汚なう。一般Iζ遣元洗浄はソーダ灰
や苛性ソーダを併用してアルカリ性条件下で行われるが
、この場合はポリアミドに染色された酸性染料等が脱落
しやすく本発明では用い得ない。本発明では酸性条件下
、好ましくはS〜G、更に好ましくはS〜5のpHの浴
を用いて行う。
Next, smudge reduction cleaning. General Iζ cleaning is carried out under alkaline conditions using soda ash or caustic soda, but in this case acidic dyes etc. dyed on the polyamide tend to fall off and cannot be used in the present invention. The present invention is carried out under acidic conditions, preferably using a bath with a pH of S to G, more preferably S to 5.

ここで、pHは処理温度で測定したpHf値である。Here, pH is the pHf value measured at the treatment temperature.

pHを調整するためには、ギ酸、酢酸などの有機酸を用
いることができるが、これらに限定されない。
To adjust the pH, organic acids such as, but not limited to, formic acid and acetic acid can be used.

還元剤としては、資性条件下での還元洗浄にはハイドロ
サルファイド(Na!52o4 )は竹屑速度が速過ぎ
て望ましくなく、NaH802a CH2O・2 Ht
O1ZnSO2m CH2O@ H!0、またはZn 
CH80t m HCHO’ 2等のソジウムホルムア
ルデヒドスルホキシレートや二層化チオ尿素等、還元電
位は高いが安定性のより高い還元剤が好ましく、これら
を浴中に0.1〜8Fi/l、好ましくはO,S〜4q
/l、特に2〜4 g/lのII實で用いる。又、1元
処理は、10〜120℃、好ましくは80〜100’C
の浴中で10〜60分間、好ましくは15〜3o分間行
う。
As a reducing agent, hydrosulfide (Na!52o4) is undesirable for reducing cleaning under natural conditions because the rate of bamboo debris is too high, and NaH802a CH2O・2Ht
O1ZnSO2m CH2O@H! 0, or Zn
Reducing agents that have a high reduction potential but are more stable, such as sodium formaldehyde sulfoxylate such as CH80t m HCHO' 2 or bilayered thiourea, are preferable, and these are added to the bath at a concentration of 0.1 to 8 Fi/l, preferably is O,S~4q
/l, especially from 2 to 4 g/l. In addition, the one-source treatment is carried out at 10 to 120°C, preferably 80 to 100'C.
in a bath for 10 to 60 minutes, preferably 15 to 30 minutes.

(実施例) 実施例1 経 ポリエステルフィラメント  76d/i$8fか
らなるフィル組織の織物を公知の方法で割繊、精練、ビ
ートセットした後、210番サンドペーパーを用いて起
毛処理を行ない、立毛布帛を得た。
(Example) Example 1 A fabric with a fill structure made of warp polyester filament 76d/i$8f was split, scoured, and beat-set by a known method, and then raised using No. 210 sandpaper to create a raised fabric. I got it.

得られた立毛布帛を、高圧染色機を、用いて、漫述の分
散染料とスルホン酸ソーダ基を構造中に持つ染料とを併
用して130’cで1時間染色し、2g/l   ソジ
ウムホルムアルデヒド(商品名 レドールC) 0.2cc/1  蟻酸 lcc/1    非イオン活性剤 を含む処理液で、90℃で20分開ゃ還元洗浄処理を行
なった。
The obtained raised fabric was dyed using a high-pressure dyeing machine at 130'C for 1 hour using the described disperse dye and a dye having a sodium sulfonate group in its structure for 1 hour. Reduction cleaning treatment was performed at 90° C. for 20 minutes using a treatment solution containing formaldehyde (trade name Redol C) 0.2 cc/1 formic acid lcc/1 nonionic activator.

染色は次の処方で実施した。Staining was carried out using the following recipe.

イエロー 8%owf    8umikaron Yellow
 BE−PRD1%owf    構造中にスルホン酸
ソーダ基を持つイエロー染料 1g/l   ニツカサンソルトRM!G。
Yellow 8%owf 8umikaron Yellow
BE-PRD1%owf Yellow dye with sodium sulfonate group in its structure 1g/l Nitsuka Sunsolt RM! G.

(日華化学) (PET / N7重量比 4/1 PET 8分割) 0.1cc/1  酢酸 ブルー 8 ’# owf 1%owf 1g/l Sumikaron  Blue  8E−PRD構造
中にスルホン酸ソーダ基を持つ ブルー染料 ニッカサンソルトRMiO (日華化学) 酢酸 0.1cc/ル レッド @*owf lowf 8urnikaron  Red  8E−PRD構造
中にスルホン酸ソーダ基を持つ レッド染料 1g/l   ニツカサンソルトRM300(日華化学
) 0.1cc/1酢酸 実際の染色に先立ち還元洗浄耐久性を測定した。
(NICCA Chemical) (PET/N7 weight ratio 4/1 PET 8 division) 0.1cc/1 Acetate Blue 8'#owf 1%owf 1g/l Sumikaron Blue 8E-Blue with sodium sulfonate group in PRD structure Dye Nikka Sunsalt RMiO (Nicca Chemical) Acetic acid 0.1 cc/L Red @*owf lowf 8urnikaron Red 8E-PRD Red dye having a sodium sulfonate group in the structure 1 g/l Nikka Sunsalt RM300 (Nicca Chemical) 0. 1 cc/1 acetic acid Prior to actual dyeing, reduction washing durability was measured.

前記立毛布帛を用いて、硫安0.5g/lを併用して、
スルホン酸ソーダ基を構造中に持つ染料で1 ’S O
℃1時間染色し、布帛の染色前後の最大吸収波長でのに
/8値を測定し、還元洗浄耐久性を前記した下式で算出
した。
Using the raised fabric, 0.5 g/l of ammonium sulfate was used,
A dye with a sodium sulfonate group in its structure, 1'S O
The fabric was dyed for 1 hour at °C, and the /8 value was measured at the maximum absorption wavelength of the fabric before and after dyeing, and the reduction washing durability was calculated using the formula below.

この様にして分散染料とS造中iこスルホン舅ソーダ基
を染料(以下アニオン染料と呼方)とを同浴で染色しポ
リエステルサイドとナイロンサイドに堅牢に染色せしめ
た。又、比較例として、スルホン履ソーダ基を構造中に
持つ染料を併用し、;いもの、これjζ代えて染料(イ
エロー: Aizenムn1lon Yellow 5
RL 、ブルー: Nylcsan BlueNFGL
 、レッド: Nylosan Red 2RBL )
を用い、他は全く同唐に処理したものを用意した。
In this manner, the polyester side and nylon side were dyed with the disperse dye and the sulfone soda group dye (hereinafter referred to as anionic dye) in the same bath to dye the polyester side and the nylon side firmly. In addition, as a comparative example, a dye having a sulfonic acid group in its structure was used in combination;
RL, Blue: Nylcsan BlueNFGL
, Red: Nylosan Red 2RBL)
was used, and other treatments were prepared in exactly the same way.

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

溝下表中のjj!塵白化の評価は試験布の立毛面を、手
振型染色物、1!擦堅牢度試験機を用いて、荷重=aa
gでJl擦市に湿潤状態の綿布を用いて4(H)回、1
i!擦し白化の状態を肉眼にて判定した。
jj in mizonoshita table! For the evaluation of dust whitening, the raised side of the test cloth was hand-wave dyed, 1! Using a rubbing fastness tester, load = aa
4 (H) times, 1 time using a damp cotton cloth on Jl Ruiichi at g.
i! The state of whitening was determined visually.

第1表に示す如く本発明によれば、昇華堅牢度に優れ、
摩擦白化現象の少ない良好な結果が得られる。
As shown in Table 1, the present invention has excellent sublimation fastness,
Good results with less friction whitening phenomenon can be obtained.

(以y余白) (発明の効果) 本発明によれば、ポリエステル及びポリアミドと云う全
く染色性の異なった素材を一浴で均一に染色可能であっ
て、しかもその染色堅牢度も実用上充分な程度が得られ
る。よって、ポリエステルとポリアミドの各々の機能を
兼備した布帛の用途が広がり、その有用性は明らかであ
る。
(The following is a blank space) (Effects of the Invention) According to the present invention, materials with completely different dyeing properties, such as polyester and polyamide, can be uniformly dyed in one bath, and the color fastness is sufficient for practical use. degree is obtained. Therefore, the uses of fabrics that have both the functions of polyester and polyamide are expanding, and their usefulness is obvious.

Claims (1)

【特許請求の範囲】[Claims] (1)ポリエステル系繊維とポリアミド系繊維とを含む
複合繊維構造物を染色するに於いて、分散染料と還元洗
浄耐久性が70%以上のスルホン酸ソーダ基を構造中に
持つ染料とを併用して同浴染色し、その後酸性条件下で
還元洗浄することを特徴とする複合繊維構造物の染色方
法。
(1) When dyeing composite fiber structures containing polyester fibers and polyamide fibers, a disperse dye and a dye having a sodium sulfonate group in its structure and having resistance to reduction washing of 70% or more are used in combination. 1. A method for dyeing a composite fiber structure, which is characterized by dyeing in the same bath, followed by reduction washing under acidic conditions.
JP2176792A 1990-07-03 1990-07-03 Dyeing of conjugate structure Pending JPH0465586A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2176792A JPH0465586A (en) 1990-07-03 1990-07-03 Dyeing of conjugate structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2176792A JPH0465586A (en) 1990-07-03 1990-07-03 Dyeing of conjugate structure

Publications (1)

Publication Number Publication Date
JPH0465586A true JPH0465586A (en) 1992-03-02

Family

ID=16019930

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2176792A Pending JPH0465586A (en) 1990-07-03 1990-07-03 Dyeing of conjugate structure

Country Status (1)

Country Link
JP (1) JPH0465586A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005187984A (en) * 2003-12-26 2005-07-14 Daiichi Kasei Kk Method for dyeing conjugate fiber raw material
JP2008509290A (en) * 2004-08-04 2008-03-27 チェ,ソンフン Dyeing method of extra fine yarn and fabric woven or knitted with extra fine yarn dyed thereby

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005187984A (en) * 2003-12-26 2005-07-14 Daiichi Kasei Kk Method for dyeing conjugate fiber raw material
JP4691319B2 (en) * 2003-12-26 2011-06-01 第一化成株式会社 Dyeing method for composite fiber materials
JP2008509290A (en) * 2004-08-04 2008-03-27 チェ,ソンフン Dyeing method of extra fine yarn and fabric woven or knitted with extra fine yarn dyed thereby
EP1774087A4 (en) * 2004-08-04 2009-04-08 Sunghoon Choi A method for dyeing microfibers and fabric woven with microfibers dyed thereby

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