JPH03287883A - Production of multi-colored wool fiber product - Google Patents

Production of multi-colored wool fiber product

Info

Publication number
JPH03287883A
JPH03287883A JP2085441A JP8544190A JPH03287883A JP H03287883 A JPH03287883 A JP H03287883A JP 2085441 A JP2085441 A JP 2085441A JP 8544190 A JP8544190 A JP 8544190A JP H03287883 A JPH03287883 A JP H03287883A
Authority
JP
Japan
Prior art keywords
wool
mordant
chromium
treatment
wool fiber
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2085441A
Other languages
Japanese (ja)
Inventor
Satoru Narita
成田 哲
Masaru Yamada
優 山田
Shoji Nojima
野島 昌治
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.)
Kurabo Industries Ltd
Kurashiki Spinning Co Ltd
Original Assignee
Kurabo Industries Ltd
Kurashiki Spinning Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kurabo Industries Ltd, Kurashiki Spinning Co Ltd filed Critical Kurabo Industries Ltd
Priority to JP2085441A priority Critical patent/JPH03287883A/en
Publication of JPH03287883A publication Critical patent/JPH03287883A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the subject product having excellent shrinkproofness, color fastness and multi-color effect by subjecting a fiber product composed of chrome-mordanted wool and non-mordanted wool to shrinkproofing treatment, treating the product with an acidic mordant dye and then treating with a mordant metal other than chromium. CONSTITUTION:A wool fiber product composed of chrome-mordanted wool and non-mordanted wool is subjected to shrinkproofing treatment (e.g. by oxidizing with chlorine or oxygen) and the treated product is treated with an acidic mordant dye and then with a mordant metal compound other than chromium (e.g. cobalt, zinc, copper, nickel or tin) to obtain the objective multi-colored wool fiber product having excellent shrinkproofness and color fastness.

Description

【発明の詳細な説明】 産業上の利用分野 の製法に関する。[Detailed description of the invention] Industrial applications Concerning the manufacturing method.

従来の技術 従来から、ヘアミックス調の異色効果を発揮すると共に
、防縮性を有する多色羊毛繊維製品を製法する方法とし
ては、バラ毛やスライバー等の糸の原料を塩素酸化法や
酸素酸化法による防縮処理に付した後、先染めによりブ
レンドし、これを布帛化する方法、および所謂「マルチ
クローム法」等によって染色した羊毛繊維製品を重亜硫
酸塩付加ウレタンポリマー等の樹脂を用いる防縮加工処
理に付す方法等が知られている。
Conventional technology Traditionally, methods for manufacturing multicolored wool fiber products that exhibit a unique hair mix-like effect and have shrink-proofing properties include chlorine oxidation and oxygen oxidation methods for yarn raw materials such as loose wool and sliver. A method in which wool fiber products dyed by a method such as the so-called "multichrome method" is subjected to a shrink-proofing treatment using a resin such as a bisulfite-added urethane polymer, and then blended by yarn dyeing and made into a fabric. There are known methods for applying the same.

しかしながら、前者においては、染色から布帛になるま
で多くの工程を必要とし、各染色工程ごとに機台の切換
えや清掃も必要となり、さらに製造工程中に多量の屑を
発生するので生産歩留りが低下するだけでなく、現在量
も重要な要件となっている「クイックデリバリ−」や「
小ロツト化」の要請に応えることができないという難点
がある。
However, the former method requires many processes from dyeing to fabric production, requires changing and cleaning the machine after each dyeing process, and also generates a large amount of waste during the manufacturing process, which reduces production yield. "Quick delivery" and "
The problem is that it cannot meet the demand for smaller lots.

また、後者においては、羊毛繊維製品に十分な防縮性を
付与するためには、高度の樹脂加工度を必要とするため
に、羊毛特有の柔軟な風合が損なわれるという欠点があ
る。
In addition, the latter method requires a high degree of resin processing in order to impart sufficient shrink-proofing properties to wool fiber products, which has the disadvantage that the soft feel peculiar to wool is impaired.

なお、クロイマシンを用いて布帛状の羊毛繊維製品を酸
化処理によって防縮加工する方法が提案されているが、
対象が無地染品やプリント下生地であり、該方法によっ
ては、ヘアミックス調の異色感を発揮する防縮性の羊毛
繊維製品を得ることはできない。
In addition, a method has been proposed for shrink-proofing fabric-like wool fiber products by oxidation treatment using a croiming machine.
The targets are plain dyed products and printed fabrics, and depending on the method, it is not possible to obtain a shrink-proof wool fiber product that exhibits a unique color feel similar to that of a hair mix.

発明が解決しようとする課題 この発明は、従来の上記問題点を解決し、優れた防縮性
と染色堅牢性を兼有すると共に、羊毛特有の柔軟な風合
を損なうことなく、多様なヘアミックス調の異色効果を
発揮する多色羊毛繊維製品を提供するためになされたも
のである。
Problems to be Solved by the Invention The present invention solves the above-mentioned conventional problems, and has both excellent shrink-proofing properties and dyeing fastness, and can be used in various hair mix tones without impairing the soft texture peculiar to wool. This was done in order to provide a multicolored wool fiber product that exhibits a unique color effect.

課題を解決するための手段 即ちこの発明は、クロム媒染羊毛および未媒染羊毛から
戊る羊毛繊維製品を防縮処理に付した後、酸性媒染染料
を用いて処理し、次いで、該酸性媒染染料と反応して有
色不溶性化合物を生成するクロム以外の媒染金属化合物
を用いてさらに処理することを特徴とする多色羊毛繊維
製品の製法に関する。
A means for solving the problem, that is, the present invention, is to subject wool fiber products made from chromium mordant wool and unmordanted wool to anti-shrunk treatment, and then to treat them with an acidic mordant dye, and then to react with the acidic mordant dye. The present invention relates to a process for producing multicolored wool fiber products, characterized in that the process is further treated with a mordant metal compound other than chromium, which produces a colored insoluble compound.

クロム媒染羊毛および未媒染羊毛から戊る羊毛繊維製品
は常套のマルチクローム法に従って製造すればよい。
Wool fiber products made from chromium mordanted wool and unmordanted wool may be produced according to conventional multichrome processes.

クロム化合物としては重クロム酸カリウム、重クロム酸
ナトリウム等を使用する。
Potassium dichromate, sodium dichromate, etc. are used as the chromium compound.

クロム処理に付す前の羊毛は通常、非イオン系もしくは
アニオン系の界面活性剤を使用して精練する。
Prior to chromium treatment, wool is usually scoured using nonionic or anionic surfactants.

クロム媒染羊毛と未媒染羊毛から戒る羊毛繊維製品の形
態はブレンド糸、ブレンド糸を用いた織物もしくは編物
等いずれであってもよく、また両者の混用比は所望によ
り適宜選択すればよい。
The form of the wool fiber product, which consists of chromium mordanted wool and unmordanted wool, may be blended yarns, woven or knitted fabrics using blended yarns, and the mixing ratio of the two may be appropriately selected as desired.

羊毛繊維製品の防縮処理は、従来から知られている羊毛
の防縮法を適宜利用しておこなえばよいが、特に好適な
方法は、塩素ガス、次亜塩素酸ソーダ、ジクロロイソシ
アヌル酸ソーダ等を使用する塩素酸化法、および過マン
ガン酸カリウム、過硫酸、過硫酸カリ等を使用する酸素
酸化法である。
The shrink-proofing treatment of wool fiber products can be carried out by appropriately utilizing conventionally known wool shrink-proofing methods, but particularly suitable methods include using chlorine gas, sodium hypochlorite, sodium dichloroisocyanurate, etc. The chlorine oxidation method uses potassium permanganate, persulfuric acid, potassium persulfate, etc.

この防縮処理によってクロム媒染羊毛中のクロム含有量
はほとんど影響を受けず、以後の異色染色に必要なりロ
ムはほぼ定量的に保持される。このことは、酸化反応が
羊毛繊維周辺部のジサルファイト結合において集中的に
起こり、クロム媒染の際の配位活性点に影響を及ぼさな
いことを意味する。
This anti-shrink treatment hardly affects the chromium content in the chromium mordanted wool, and the chromium, which is required for subsequent different color dyeing, is retained almost quantitatively. This means that the oxidation reaction occurs intensively in the disulfite bonds around the wool fibers and does not affect the coordination active sites during chromium mordanting.

また、この防縮処理によって、羊毛の臨界表面張力が増
加するので、種々の風合調整剤、例えばシリコン系柔軟
仕上剤、ポリアミド樹脂等を使用することができる。例
えば、特定の酵素を用いて処理することによって、羊毛
繊維製品にカシミア調の風合を付与することができる(
特公平1−54471号明細書参照)。
Moreover, since the critical surface tension of the wool is increased by this shrink-proofing treatment, various hand control agents such as silicone softeners, polyamide resins, etc. can be used. For example, a cashmere-like texture can be imparted to wool fiber products by treating them with specific enzymes (
(Refer to the specification of Japanese Patent Publication No. 1-54471).

上記のようにして得られる防縮性羊毛繊維製品は先ず、
酸性媒染染料を用いて処理した後、該酸性媒染染料と反
応して有色不溶性化合物を生成するクロム以外の媒染金
属化合物を用いてさらに処理する。
The shrink-proof wool fiber product obtained as above is firstly
After treatment with an acidic mordant dye, further treatment is performed with a mordant metal compound other than chromium that reacts with the acidic mordant dye to form a colored insoluble compound.

酸性媒染染料としては、クロム化合物およびクロム以外
の媒染金属化合物によって媒染される染料を使用すれば
よく、例えば山田化学工業株式会社の市販品rchro
me Yellow A S J、rMordantY
ellow l 02J、rMordant Blue
 LMJ、rchrome Red 5 G J、rc
hrome Navy 3 RM、1、r Chrom
e B rain L E JおよびrMordant
 Green501」、三井東圧株式会社の市販品rM
itsutChrome Fast Brown BX
J並びに住友化学工業株式会社の市販品r S unc
hromine G rey 3 B L J等が挙げ
られる。
As the acidic mordant dye, dyes that are mordanted with chromium compounds and mordant metal compounds other than chromium may be used; for example, the commercially available product rchrom from Yamada Chemical Industry Co., Ltd.
me Yellow A S J, rMordantY
yellow l 02J, rMordant Blue
LMJ, rchrome Red 5 G J, rc
chrome Navy 3 RM, 1, r Chrom
e Brain L E J and rMordant
Green501”, commercial product rM of Mitsui Toatsu Co., Ltd.
ItsutChrome Fast Brown BX
J and Sumitomo Chemical Co., Ltd.'s commercial product r S unc
Examples include Hromine Gray 3 B L J.

羊毛繊維の一部はクロム化合物によって媒染されている
ので、酸性媒染染料は染着される。従って、通常の後媒
染の場合のように、染料の吸尽を向上させるために染浴
を極端な酸性にする必要はなく、−膜内な羊毛用染料の
染色条件と同一の条件を採用すればよい。
Since some of the wool fibers are mordanted with chromium compounds, acid mordant dyes are dyed. Therefore, it is not necessary to make the dyebath extremely acidic in order to improve the exhaustion of the dye, as is the case with normal post-mordanting - the dyeing conditions identical to those for wool dyes in the membrane should be adopted. Bye.

このため、核酸性媒染染料と反応して有色不溶性化合物
を生成するクロム以外の媒染金属化合物を用いる処理は
、酸性媒染染料処理を行う浴と同−の浴でおこなうこと
ができる。
Therefore, the treatment using a mordant metal compound other than chromium that reacts with the nucleic acid mordant dye to produce a colored insoluble compound can be carried out in the same bath as the bath in which the acidic mordant dye treatment is carried out.

例えば、初俗のpHを弱酸性から中性の範囲に調整し、
常套の均染剤(例えば、「ニューポン5DJ(日華化学
工業株式会社の市販品)、「レベジン200J(日或化
或株式会社の市販品)等)を添加し、浴温を1℃/分で
昇温させ、約30〜40分間煮沸させた後、クロム以外
の媒染金属化合物を染浴中に添加し、煮沸をさらに約l
O〜30分間続行することによって、未媒染羊毛に吸収
された酸性媒染染料が安定化されると共に堅牢な異色染
が可能となる。
For example, adjusting the initial pH from weakly acidic to neutral,
Add a conventional leveling agent (for example, "Newpon 5 DJ (commercial product from Nichika Kagaku Kogyo Co., Ltd.),""Levezin 200J (commercial product from Nichika Kagaku Co., Ltd.), etc.), and increase the bath temperature by 1°C/min. After raising the temperature at
By continuing for 0 to 30 minutes, the acidic mordant dye absorbed into the unmordanted wool is stabilized and fast different color dyeing becomes possible.

クロム以外の媒染金属化合物は酸性媒染染料と反応して
安定な有色化合物を生成させる化合物であり、該有色化
合物を適宜選定することによって多様なヘアミックス調
の異色効果を得ることかできる。
Mordant metal compounds other than chromium are compounds that react with acidic mordant dyes to produce stable colored compounds, and by appropriately selecting the colored compounds, it is possible to obtain a variety of unique hair mix-like effects.

このような媒染金属としては、コバルト、亜鉛、銅、ニ
ッケル、スズ、鉄およびカドミウムの化合物が挙げられ
、具体的には以下の化合物が例示される。酢酸塩として
酢酸コバルト、酢酸鉄、酢酸、1 銅、酢酸ニッケル等、塩化物として塩化亜鉛、塩化銅、
塩化ニッケル等、また、硫酸塩として硫酸銅、硫酸鉄等
である。また、含銅フィックス剤として市販されている
もの(例えば「カブラミン700J(日本染化工業株式
会社の市販品))も利用できる。
Examples of such mordant metals include compounds of cobalt, zinc, copper, nickel, tin, iron, and cadmium, and specific examples include the following compounds. Acetate salts include cobalt acetate, iron acetate, acetic acid, copper, nickel acetate, etc. Chlorides include zinc chloride, copper chloride,
Nickel chloride, etc., and sulfates such as copper sulfate and iron sulfate. Also, commercially available copper-containing fixing agents (for example, "Cabramin 700J (commercial product of Nippon Someka Kogyo Co., Ltd.)" can also be used.

上記の媒染金属化合物を用いる処理は、上述のようにし
て染浴中でおこなうのが一般的であるが、酸性媒染染料
を用いて染色した後、パディング法によっておこなって
もよい。
The treatment using the mordant metal compound described above is generally carried out in a dye bath as described above, but it may also be carried out by a padding method after dyeing with an acidic mordant dye.

本発明に係る上述の羊毛繊維製品の染色法にさらに従来
のスルファミン酸、アミノクロロアリル化合物または多
価フェノール等を用いて羊毛繊維を処理することによっ
て該繊維に含まれるアミノ基等の官能基を封鎖して染色
を抑制する防染処理法を組合わせることによって、多彩
な異色効果を現出させてもよい。
In addition to the above-described dyeing method for wool fiber products according to the present invention, functional groups such as amino groups contained in the fibers can be removed by treating wool fibers with conventional sulfamic acid, aminochloroallyl compounds, polyhydric phenols, etc. A variety of different color effects may be produced by combining resist dyeing treatment methods that block and suppress dyeing.

なお、あらかじめ防縮加工を施した羊毛原料を上述の染
色処理を含む工程に付すことによって、防縮性を有する
多色羊毛繊維製品を製造することが可能であるが、この
場合には布帛の状態で縮絨加工はできない。
Note that it is possible to produce multicolored wool fiber products with shrink-proof properties by subjecting wool raw materials that have been pre-shrink-proof to the process including the dyeing process described above, but in this case, it is possible to produce a multi-colored wool fiber product with shrink-proof properties. Fulling processing is not possible.

以下、本発明を実施例によって説明する。Hereinafter, the present invention will be explained by examples.

実施例1 マルチクローム染色法によってクロム媒染羊毛/未処理
羊毛(50150”)のブレンド糸(1/30)を作威
し、該ブレンド糸に双糸加工を施して次の特性を有する
織物を製造した: 2/30  (Z47o、5430) 地経糸数; 3268本 打入数;44本 目    付;4519 2/2  /斜文 該織物を常套の整理工程を通し、液流染色機を用いて次
の手順に従って防縮処理をおこなった(浴比1 :20
)。
Example 1 A blended yarn (1/30) of chromium mordanted wool/untreated wool (50150'') was produced by the multi-chrome dyeing method, and the blended yarn was subjected to double-thread processing to produce a fabric with the following characteristics. Made: 2/30 (Z47o, 5430) Number of ground warp threads: 3268 Number of stitches: 44th thread Attachment: 4519 2/2 / Diagonal The fabric was passed through the usual sorting process and then dyed using a jet dyeing machine as follows: Preshrinkage treatment was performed according to the procedure (bath ratio 1:20
).

(i)硫酸ナトリウム10%owfおよび「ハイライト
60 GJ(日産化学株式会社製ジクロロイソシアヌル
酸塩6.0%owf含有水溶液(20℃)に該織物を2
0分間接触させる(該水溶液のpHは酢酸を用いて4.
5に調整する)。
(i) The fabric was placed in an aqueous solution (20°C) containing 10% owf of sodium sulfate and ``Highlight 60 GJ (manufactured by Nissan Chemical Co., Ltd.) containing dichloroisocyanurate 6.0% owf.
(The pH of the aqueous solution was adjusted to 4.0 using acetic acid.)
(adjust to 5).

(ii)該水溶液の温度を15分間かけて40℃まで上
昇させ、60分間維持した後、硫酸水素ナトリウム10
%owfを浴中へ添加し、さらに10分間処理する。
(ii) Raise the temperature of the aqueous solution to 40°C over 15 minutes, maintain it for 60 minutes, and then
%owf into the bath and process for an additional 10 minutes.

(ii)防縮処理に付した該織物を20℃で水洗する。(ii) The fabric subjected to the shrink-proofing treatment is washed with water at 20°C.

上記の防縮処理に付した該織物の試料を120℃で1時
間乾燥した後、硝酸分解処理に付し、試料中のクロム含
有率を原子吸光光度法によって定量したところ、0,2
8%owfであった。
A sample of the fabric subjected to the above-mentioned shrink-proofing treatment was dried at 120°C for 1 hour and then subjected to nitric acid decomposition treatment, and the chromium content in the sample was determined by atomic absorption spectrometry.
It was 8% owf.

上記の防縮織物を、液流染色機を使用し、次の条件下で
染色した。
The above shrink-proof fabric was dyed using a jet dyeing machine under the following conditions.

使用染料 イルガラン・イエロー 2 G L ”)0.3%ow
fイルガラン・ブラウン 2 RL (2)0.1%o
vfモルダント・ブルー LM(3)  0.3%ow
fニ−ポン 5D(4)      1% owf(1
)チバガイギー社製含金属染料r I rgalanY
ellow 2 G L J (2)チバガイギー社製含金属染料r I rgala
nBrown  2RLJ (3)山田化学工業株式会社製酸性媒染染料rMord
ant Brown LMJ(4)111化学株式会社
製羊毛用均染剤初浴を40℃から昇温させ(1℃/分)
、煮沸を40分間おこなった後、酢酸コバルト0.15
%owfを加え、煮沸処理をさらに20分間続行する。
Dye used: Irgalan Yellow 2GL”) 0.3%ow
f Ilgalan Brown 2 RL (2) 0.1%o
vf mordant blue LM (3) 0.3%ow
f kneepon 5D(4) 1% owf(1
) Ciba Geigy metal-containing dye rI rgalanY
yellow 2 G L J (2) Metallic dye r I rgala manufactured by Ciba Geigy
nBrown 2RLJ (3) Acidic mordant dye rMord manufactured by Yamada Chemical Industry Co., Ltd.
ant Brown LMJ (4) 111 Kagaku Co., Ltd. Level dyeing agent for wool Initial bath heated from 40°C (1°C/min)
, after boiling for 40 minutes, cobalt acetate 0.15
%owf is added and the boiling process is continued for an additional 20 minutes.

上記の染色処理に付した織物を、シリコーン系柔軟仕上
剤を用いるパディングを含む常套の仕上げ工程に通すこ
とによって、柔軟な風合を示すブルーとベージュの混色
したヘアクロス調の織物を製造した。
The dyed fabric was subjected to a conventional finishing process including padding with a silicone fabric softener to produce a haircloth-like fabric in a mixed color of blue and beige with a soft texture.

得られたヘアクロス調織物(I)の防縮性(電気洗濯機
法による収縮)、洗濯変退色性および摩擦堅牢度を調べ
、結果を表−1に示す。
The resulting haircloth-like fabric (I) was examined for shrinkage resistance (shrinkage by electric washing machine method), discoloration and fading resistance after washing, and fastness to abrasion, and the results are shown in Table 1.

実施例2 防縮処理を以下の手順でおこなう以外は、実施例1と同
様にヘアミックス調の織物を製造した:(iXNH4)
*SOa  2649/12含有水溶液(2O℃)にク
ロム媒染羊毛/未処理羊毛のブレンド糸よりなる実施例
1と同様の織物を10分間接触させた後、KMno、6
%owfを添加し、60分間維持する。
Example 2 A hair mix-like fabric was produced in the same manner as in Example 1, except that the shrink-proofing treatment was performed in the following procedure: (iXNH4)
* After contacting a woven fabric similar to Example 1 made of a blended yarn of chromium mordanted wool/untreated wool for 10 minutes with an aqueous solution containing SOa 2649/12 (20°C), KMno, 6
Add %owf and hold for 60 minutes.

(1)浴温を15分間かけて40℃まで上昇させ、60
分間維持した後、20℃で水洗する。
(1) Raise the bath temperature to 40℃ over 15 minutes,
After keeping it for a minute, it is washed with water at 20°C.

(玩)次いで、織物を、硫酸水素ナトリウムlO%ow
fおよび酢酸10%owf含有水溶液と接触させ、浴温
を10分間かけて70℃まで上昇させ、20分間維持し
た後、20℃で水洗する。実施例1と同様にクロム含有
率を定量した結果0.32%owfであった。
(Toy) Next, the fabric was treated with sodium hydrogen sulfate lO%ow
The bath temperature was raised to 70°C over 10 minutes, maintained for 20 minutes, and then washed with water at 20°C. The chromium content was determined in the same manner as in Example 1 and was found to be 0.32% owf.

染色して得られたヘアミックス調織物(II)の防縮性
、洗濯変退色性および摩擦堅牢度を調べ、結果を表−1
に示す。
The shrink resistance, washing discoloration and fading resistance, and abrasion fastness of the hair mix-like fabric (II) obtained by dyeing were investigated, and the results are shown in Table 1.
Shown below.

比較例1 実施例1と同様の織物を用い、同染料しサイプで染色し
た。被染色布のクロム含有率は0°32%ovfであっ
た。
Comparative Example 1 The same fabric as in Example 1 was used and dyed with the same dye and sipes. The chromium content of the fabric to be dyed was 0°32% ovf.

得られたヘアクロス調(I′)の防縮性、洗濯変退色性
および摩擦堅牢度を表−1に示す。
Table 1 shows the shrink resistance, washing discoloration and fading properties, and abrasion fastness of the hair cloth look (I') obtained.

とができるので、製造工程中において縮絨加工等羊毛製
品の特性を有効に利用することができる。
Therefore, the characteristics of wool products such as fulling can be effectively utilized during the manufacturing process.

Claims (1)

【特許請求の範囲】 1、クロム媒染羊毛および未媒染羊毛から成る羊毛繊維
製品を防縮処理に付した後、酸性媒染染料を用いて処理
し、次いで、該酸性媒染染料と反応して有色不溶性化合
物を生成するクロム以外の媒染金属化合物を用いてさら
に処理することを特徴とする多色羊毛繊維製品の製法。 2、防縮処理を塩素酸化または酸素酸化によっておこな
う請求項1記載の方法。 3、媒染金属化合物がコバルト、亜鉛、銅、ニッケル、
スズ、鉄およびカドミウムの化合物から成る群から選択
される化合物である請求項1記載の方法。 4、請求項1から3いずれかに記載の方法によって得ら
れる多色羊毛繊維製品。
[Scope of Claims] 1. Wool fiber products made of chromium mordant wool and unmordanted wool are subjected to anti-shrunk treatment, and then treated with an acidic mordant dye, and then reacted with the acidic mordant dye to form a colored insoluble compound. A process for producing multicolored wool textile products, characterized by further treatment with a mordant metal compound other than chromium, which produces 2. The method according to claim 1, wherein the shrink-proofing treatment is performed by chlorine oxidation or oxygen oxidation. 3. The mordant metal compound is cobalt, zinc, copper, nickel,
2. The method of claim 1, wherein the compound is selected from the group consisting of compounds of tin, iron and cadmium. 4. A multicolored wool fiber product obtained by the method according to any one of claims 1 to 3.
JP2085441A 1990-03-30 1990-03-30 Production of multi-colored wool fiber product Pending JPH03287883A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2085441A JPH03287883A (en) 1990-03-30 1990-03-30 Production of multi-colored wool fiber product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2085441A JPH03287883A (en) 1990-03-30 1990-03-30 Production of multi-colored wool fiber product

Publications (1)

Publication Number Publication Date
JPH03287883A true JPH03287883A (en) 1991-12-18

Family

ID=13858955

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2085441A Pending JPH03287883A (en) 1990-03-30 1990-03-30 Production of multi-colored wool fiber product

Country Status (1)

Country Link
JP (1) JPH03287883A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0665875A (en) * 1992-08-21 1994-03-08 Kanebo Ltd Production of modified wool woven fabric
EP1164219A1 (en) * 2000-06-15 2001-12-19 Sumitomo Corporation A method for manufacturing washable wool fabric
WO2001062215A3 (en) * 2000-02-25 2002-01-17 Procter & Gamble Hair treatment compositions and their use
JP2002275768A (en) * 2001-03-22 2002-09-25 Yamada Chem Co Ltd Method for dyeing synthetic polyamide fiber
JP2007518884A (en) * 2003-09-18 2007-07-12 マルワ インダストリーズ リミテッド Method for indigo dyeing of wool and wool blends
JP2016017242A (en) * 2014-07-07 2016-02-01 山田化学工業株式会社 Near infrared reflective polyamide fiber

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0665875A (en) * 1992-08-21 1994-03-08 Kanebo Ltd Production of modified wool woven fabric
WO2001062215A3 (en) * 2000-02-25 2002-01-17 Procter & Gamble Hair treatment compositions and their use
EP1164219A1 (en) * 2000-06-15 2001-12-19 Sumitomo Corporation A method for manufacturing washable wool fabric
JP2002275768A (en) * 2001-03-22 2002-09-25 Yamada Chem Co Ltd Method for dyeing synthetic polyamide fiber
JP2007518884A (en) * 2003-09-18 2007-07-12 マルワ インダストリーズ リミテッド Method for indigo dyeing of wool and wool blends
JP4750555B2 (en) * 2003-09-18 2011-08-17 マルワ インダストリーズ リミテッド Method for indigo dyeing of wool and wool blends
JP2016017242A (en) * 2014-07-07 2016-02-01 山田化学工業株式会社 Near infrared reflective polyamide fiber

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