JPS6245793A - Resist style of fiber structure - Google Patents

Resist style of fiber structure

Info

Publication number
JPS6245793A
JPS6245793A JP60185458A JP18545885A JPS6245793A JP S6245793 A JPS6245793 A JP S6245793A JP 60185458 A JP60185458 A JP 60185458A JP 18545885 A JP18545885 A JP 18545885A JP S6245793 A JPS6245793 A JP S6245793A
Authority
JP
Japan
Prior art keywords
dye
fiber
type reactive
resist
protein
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
JP60185458A
Other languages
Japanese (ja)
Other versions
JPH0258396B2 (en
Inventor
衣笠 順三
秀生 松井
大東 清光
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 JP60185458A priority Critical patent/JPS6245793A/en
Publication of JPS6245793A publication Critical patent/JPS6245793A/en
Publication of JPH0258396B2 publication Critical patent/JPH0258396B2/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、セルロース系、繊維と蛋白質系、1維とより
なる繊維構造物の防染方法に関するものである0 (従来の技術) 従来、セルロース系繊維と蛋白質系繊維の抜染用地染に
関しては、通常ウィンス染色機又は、液流染色機などに
よる吸尽染色法が主体に行われており、パディング法は
余り実施されていない。これは、パディング法ではセル
ロース系繊維と蛋白質系i維とを均一に染色することが
困難であるためである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for resist dyeing a fibrous structure consisting of cellulose, fiber and protein, and one fiber.0 (Prior Art) Conventionally, Regarding ground dyeing for discharge printing of cellulose fibers and protein fibers, the exhaust dyeing method using a Winx dyeing machine or a jet dyeing machine is usually carried out, and the padding method is not often carried out. This is because it is difficult to uniformly dye cellulose fibers and protein fibers using the padding method.

又、吸尽法にて地染した染色物を抜染する際に反応性染
料を用いて染色したのでは抜染が離しくスレン染料を用
いた染色方法が実施されている。
In addition, when discharging a dyed product ground-dyed by the exhaustion method, the discharge is difficult to achieve if a reactive dye is used to dye the product, so a dyeing method using a threne dye has been implemented.

しかしながら、この方法は、染液の管理等に複雑な工程
を要し、また群間な差し色を得ることが催しい。
However, this method requires complicated steps such as controlling the dye liquor, and it is difficult to obtain distinct colors between groups.

(発明が解決しようとする問題点) 本発明の目的は、発色性に優れた、セルロース系繊維と
蛋白質系繊維とよりなる繊維構造物の防染方法を提供す
ることである。
(Problems to be Solved by the Invention) An object of the present invention is to provide a method for resist dyeing a fiber structure made of cellulose fibers and protein fibers, which has excellent color development.

又、他の目的は斯かる防染を、均染性に優れたパディン
グ法による地染と、簡易な捺染法の組合せにより行なう
方法を提供することである。
Another object of the present invention is to provide a method for carrying out such resist dyeing by a combination of ground dyeing using a padding method with excellent level dyeing properties and a simple printing method.

(問題点を解決するための手段) 本発明方法は、セルロース系繊維と蛋白質系繊維とより
なる繊維構造物に、ビニルスルホン型反応性染料を含有
する中性乃至酸性の染液を付与した後、所定時間放置し
、次いでモノクロロトリアジン型反応性染料とアルカリ
剤とビニルスルホン型反応性染料用防染剤とを含有する
捺染糊で印捺し、乾燥、蒸熱処理後、更にアルカリ溶液
を付与して蒸熱処理することを特徴とするものである。
(Means for Solving the Problems) The method of the present invention involves applying a neutral to acidic dye solution containing a vinyl sulfone type reactive dye to a fiber structure made of cellulose fibers and protein fibers. , left to stand for a predetermined time, then printed with a printing paste containing a monochlorotriazine type reactive dye, an alkaline agent, and a resist dye for vinylsulfone type reactive dyes, dried and steamed, and then further applied with an alkaline solution. It is characterized by steam treatment.

本発明で使用するセルロース系繊維としては、綿、再生
繊維系繊維、麻等が挙げられる。
Examples of cellulose fibers used in the present invention include cotton, recycled fibers, hemp, and the like.

また、蛋白質系ト」維としては、羊毛、絹等が挙げられ
る。セルロース系繊維と蛋白質系繊維との混合率は通常
セルロース系繊維55〜90重量%、好ましくは70〜
85重量%と、蛋白質系」維10〜45重量%、好まし
くは15〜30重遺%である。両者の混合は、混紡、交
撚、交織、交編のいずれでもよいが、特に混紡が好まし
い。繊維構造物としては、織物が特に好ましい。
In addition, examples of protein-based fibers include wool, silk, and the like. The mixing ratio of cellulose fiber and protein fiber is usually 55 to 90% by weight of cellulose fiber, preferably 70 to 90% by weight.
85% by weight, and 10-45% by weight of protein-based fibers, preferably 15-30% by weight. The mixture of the two may be blended spinning, twisted twisting, mixed weaving, or mixed knitting, but blended spinning is particularly preferred. As the fiber structure, woven fabrics are particularly preferred.

本発明に適用するビニルスルホン型反応性染料は通常の
ものが使用され例えばヘキスト社のレマゾール染料、住
人化学−のスミフィックス、三井東圧■のセルマゾール
、三菱化成−のダイヤミラ等が挙げられる。染液の濃度
は特に限定されず染料の種類、色等により適宜決定すれ
ばよい。染液のpHは中性乃至酸性に調整する必要があ
り、T)H8以下、好ましくは7以下、更に好ましくは
6以下、特に好ましくは5以下である。pHの調整は通
常酢酸へキサメタリン酸ソーダ或いは第1リン酸ソーダ
等で行なう。染液の温度は特に限定されず通常の温度で
よく、一般的には20〜30℃でよい。
Conventional vinyl sulfone type reactive dyes are used, such as Remazol dye manufactured by Hoechst, Sumifix manufactured by Sumitomo Chemical, Selmazole manufactured by Mitsui Toatsu, and Diamira manufactured by Mitsubishi Kasei. The concentration of the dye solution is not particularly limited and may be appropriately determined depending on the type of dye, color, etc. The pH of the dye liquor must be adjusted to be neutral or acidic, and T)H is 8 or less, preferably 7 or less, more preferably 6 or less, particularly preferably 5 or less. The pH is usually adjusted using acetic acid, sodium hexametaphosphate, dibasic sodium phosphate, or the like. The temperature of the dye liquor is not particularly limited and may be a normal temperature, generally 20 to 30°C.

染液の付与はパッディング法、ローラー法及びスプレー
法等のいずれでもよいが、特にパッディング法がよい。
The dye solution may be applied by any of the padding method, roller method, spray method, etc., but the padding method is particularly preferred.

染液を付与した繊維構造物は一旦巻取り放置するが通常
10〜60℃で放置する。放置時間は温度により異なる
が通常10〜50時間である。好ましくは20〜80℃
で20〜30時間放置する。
The fibrous structure to which the dye liquor has been applied is once wound up and left to stand, usually at 10 to 60°C. The standing time varies depending on the temperature, but is usually 10 to 50 hours. Preferably 20-80℃
Leave it for 20 to 30 hours.

この間に蛋白質系繊維がビニルスルホン型反応性染料に
より染着される。
During this time, the protein fibers are dyed with a vinyl sulfone type reactive dye.

放置後、繊維構造物を通常80℃以上、好ましくは10
0〜120℃で乾燥する。
After standing, the fiber structure is usually heated to 80°C or higher, preferably 10°C.
Dry at 0-120°C.

乾燥後、モノクロロトリアジン型反応性染料とアル効す
剤およびビニルスルホン型反応性染料の防染剤および糊
剤よりなる捺染糊を通常行われる方法で印捺、乾燥し、
次いで蒸熱処理を行う。
After drying, a printing paste consisting of a monochlorotriazine type reactive dye, an alkaline effecting agent, a vinylsulfone type reactive dye resisting agent, and a sizing agent is printed and dried in a conventional manner,
Next, a steaming treatment is performed.

本発明に適用するモノクロロトリアジン染料は、通常の
ものが使用され、例えば、チバガイギー社(77シバク
ロン染料、101社のプロジオン染料等が挙げられる。
Common monochlorotriazine dyes can be used in the present invention, such as Ciba-Geigy's (77 Cibacron dye, 101 Prodione dye, etc.).

防染剤Ji、ビニルスルホン型反応性染料に対するもの
で、有機スルホン酸塩系の薬品が使用され、例えば開成
化学−社のレジストールHW8、林化学−社のユニスト
ン凡R−50等が挙げられる。
The resist dye Ji is for vinyl sulfone-type reactive dyes, and organic sulfonate-based chemicals are used, such as Kaisei Kagaku Co.'s Registol HW8 and Hayashi Kagaku Co., Ltd.'s Unistone Bon R-50. .

これらの染料及び防染剤は、ソーダ灰、重Δ等のアルカ
リ剤、尿素を添加して、アルギン酸ソーダやCMC等の
糊剤と共に、捺染糊を作成し、印捺する。印捺、乾燥、
蒸熱処理は、通常の捺染にて行われる方法でよく、例え
ばスクリーン捺染機にて印捺、乾燥し、次いでニージャ
ーにて100℃で10分の蒸熱処理を行う。
These dyes and resist dyes are added with soda ash, an alkaline agent such as heavy Δ, and urea to form a printing paste together with a sizing agent such as sodium alginate or CMC for printing. Stamping, drying,
The steaming treatment may be performed by a method commonly used in textile printing, for example, printing is performed using a screen printing machine, drying is performed, and then steaming treatment is performed at 100° C. for 10 minutes using a kneer.

この工程により、印捺部分における地染用ビニルスルホ
ン型反応性染料が防染され、同時に、モノクロロトリア
ジン型反応性染料の着色が行われる0 次いで、アルカリ溶液、例えば15〜25℃で40〜4
3度ボーメの水ガラス溶液を付与後、通常少なくとも1
00℃1好ましくは120〜130℃の温度で蒸熱処理
をする。蒸熱処理時間は短い方が好ましく高々、1分程
度である。この蒸熱処理にて、地染のビニルスルホン型
反応性染料の着色が行われ、以後洗滌して捺染工程を終
る。
Through this process, the vinyl sulfone type reactive dye for ground dyeing in the printed area is resist-dyed, and at the same time, the monochlorotriazine type reactive dye is colored.
After application of 3 degrees Baume's water glass solution, usually at least 1
Steaming is carried out at a temperature of 00°C, preferably 120-130°C. The shorter the steaming treatment time is, the more preferable it is, and it is about 1 minute at most. This steam heat treatment is used to color the fabric with a vinyl sulfone type reactive dye, which is then washed to complete the printing process.

(発明の効果)一 本発明方法は、通常の布帛の連続染色機を使用して、セ
ルロース系繊維と蛋白質系繊維とよりなるa維構造物に
、均染性に優れ、しかも深みのある地染を与えるだけで
なく、本方法は低温染色と加熱短時間の捺染方法である
ため、本方法により得られた繊維構造物は極めて風合良
好であり、諸強力の低下も極めて低い捺染品となる。
(Effects of the Invention) 1. The method of the present invention uses an ordinary continuous fabric dyeing machine to dye an a-fiber structure made of cellulose fibers and protein fibers with excellent level dyeing properties and deep dyeing. In addition to providing dyeing, this method is a printing method that requires low temperature dyeing and short heating time, so the fiber structures obtained by this method have an extremely good texture and are printed products with extremely low strength loss. Become.

(実施例) 以下、実施例で本発明の詳細な説明する。(Example) Hereinafter, the present invention will be explained in detail with reference to Examples.

実施例ル −ヨン80重量%、羊毛20重1%の、経糸30番単糸
(細番手)、経糸密度90本/吋、緯糸30番単糸(細
番手)、偉糸密変70本/吋からなる2/2の綾組織で
目付168y/mのレーヨン、羊毛混紡織物を製織した
Examples Rouyon 80% by weight, wool 20% by weight, warp #30 single yarn (fine count), warp yarn density 90 / inch, weft #30 single yarn (fine count), fine yarn density 70 / A rayon/wool blend fabric with a basis weight of 168 y/m was woven with a 2/2 twill structure consisting of 1.

かかるレーヨン、羊毛混紡織物を80℃の場で洗った後
、酵素糊抜剤2 f/lと羊毛精練剤エマール40(花
王石けん■製>29/lを加えて60℃の湯で1時間処
理した後、充分湯洗し水洗、脱水、乾燥した。
After washing the rayon and wool blend fabric at 80°C, an enzyme desizing agent 2 f/l and a wool scouring agent Emar 40 (manufactured by Kao Soap ■>29/l) were added and treated in hot water at 60°C for 1 hour. After that, it was thoroughly washed with hot water, water, dehydrated, and dried.

次にレマゾールレッドB、601/Icヘキスト(陶製
)と尿素170 f/l、ウール用均染剤ミグレガール
WA−10(日本染化■製) 2 f/1とI)H調節
剤へキサメタリン酸ソーダ1y/4、第1リン酸ソーダ
2y/l、ニトロベンゼンスルホン酸ソーダI Q f
/1.酢酸121/l、4%のアルギン酸601/lの
地染用パッド液を作成し、該地染用パッド液でレーヨン
、羊毛混紡織物をパッドしピックアップ率70%で絞り
ロールに巻取った。かかるロールを80℃で50時間放
置した後120℃で乾燥後、シバクロンブラックBGA
(チバーガイギー(樽!+り 100 f/lとレジス
トールHW8(開成化学(陶製) 809/l及びソー
ダ灰、アルギン酸ソーダからなる捺染糊で三角形の幾何
学模様をプリントし、100℃で10分間のスチーミン
グ後43° ボーメの水ガラスをピックアップ率65%
でパッドし100℃1分間のスチーミングを行い充分に
湯洗、水洗、乾燥して、赤地に黒の幾何学模様のあるウ
ールライクのレーヨン、羊毛混紡織物を得た。得られた
捺染品の染色諸堅牢度は、第1表に示す。
Next, Remazol Red B, 601/Ic Hoechst (ceramic), urea 170 f/l, wool leveling agent Migre Girl WA-10 (manufactured by Nihon Senka ■) 2 f/1 and I) H regulator hexametaphosphoric acid Soda 1y/4, monobasic sodium phosphate 2y/l, sodium nitrobenzenesulfonate I Q f
/1. A ground dyeing pad liquid containing 121/l of acetic acid and 601/l of 4% alginic acid was prepared, and a rayon/wool blend fabric was padded with the ground dyeing pad liquid and wound onto a squeeze roll at a pickup rate of 70%. After leaving the roll at 80°C for 50 hours and drying at 120°C, Cibacron Black BGA
(Print a triangular geometric pattern with a printing paste consisting of CiverGeigy (barrel!+ri) 100 f/l, Resistol HW8 (kaisei Kagaku (ceramic) 809/l, soda ash, and sodium alginate), and dry at 100°C for 10 minutes. 43° after steaming Baume water glass pickup rate 65%
The fabric was padded with water, steamed at 100°C for 1 minute, thoroughly washed with hot water, water, and dried to obtain a wool-like rayon/wool blend fabric with a black geometric pattern on a red background. The color fastness of the obtained printed products is shown in Table 1.

実施例2 レーヨン60重量%、絹40重量%の経糸30番単糸(
細番手)経糸密度85本/吋、緯糸30番単糸(細番手
)、偉糸密度70本/吋からなる2/2の綾組織で目付
165y/rtlのレーヨン、綱混紡織物を製織した。
Example 2 Warp #30 single yarn of 60% by weight rayon and 40% by weight silk (
A rayon/rope blend fabric with a basis weight of 165 y/rtl was woven using a 2/2 twill structure consisting of a warp density of 85 yarns/inch (fine count), a weft yarn count of 30 single yarns (fine yarn count), and a warp yarn density of 70 yarns/inch.

かかるレーヨン絹混紡織物を苛性ソーダ501/lとシ
ルピットD P 2 f/1(一方社(陶製)を溶解し
た常温の水溶液中でピックアップ率65%でパッドし、
20秒間放置した後、80℃の場で洗滌し、酵素糊抜剤
2f/lを加えて、60℃の場で1時間処理し、湯洗、
脱水、乾燥して精練漂白を行った。次に、レマゾールブ
リリアントオレンジGD(ヘキスト■製)601/lと
尿素100 f/l、絹均染剤ニッサンディスバノール
M−82A(日本油脂■製) 2 f/1と、pH調節
剤、ヘキサメタリン酸ソーダ11/l。
This rayon-silk blend fabric was padded with a pick-up rate of 65% in an aqueous solution at room temperature in which 501/l of caustic soda and Silpit D P 2 f/1 (made by Ichisha (ceramic)) were dissolved.
After leaving for 20 seconds, wash at 80℃, add 2 f/l of enzyme desizing agent, treat at 60℃ for 1 hour, wash with hot water,
It was dehydrated, dried and scoured and bleached. Next, Remazol Brilliant Orange GD (manufactured by Hoechst ■) 601/l, urea 100 f/l, a silk leveling agent Nissan Disbanol M-82A (manufactured by NOF ■) 2 f/1, a pH adjuster, and hexamethalin. Acid soda 11/l.

第1リン酸ソーダ2 f/l、ニトロベンゼンスルホン
酸ソーダ10 f/l、酢酸10y/1,4%のアルギ
ン酸ソーダ60 f/lの地染用パッド液を作成し、該
地染用パッド液にレーヨン、絹混紡織物をパッドしピッ
クアップ率70%で絞った後、ロールアップして80℃
で40時間放置した。かかる後、120”Cで乾燥を行
い、シバクロンブル−3几(チバーガイギー■製) 7
09/lとレジストールHW8(可成化学■製)80y
/l及びソーダ灰、アルギン酸ソーダからなる捺染糊を
水玉模様にプリントし、100℃で10分間のスチーミ
ングの後、43°ボーメの水ガラスをピックアップ率6
5%でパッドし、100℃で1分間のスチーミングを行
い、湯洗、水洗、乾燥を施してオレンジの地にブルーの
水玉のあるシルクライクのレーヨン絹混紡織物を得た。
A ground dyeing pad solution containing 2 f/l of monobasic sodium phosphate, 10 f/l of sodium nitrobenzene sulfonate, and 60 f/l of sodium alginate containing 10 y/1.4% acetic acid was prepared, and added to the ground dyeing pad solution. After padding the rayon and silk blend fabric and squeezing it with a pick-up rate of 70%, it is rolled up and heated to 80℃.
It was left for 40 hours. After that, dry it at 120"C and use Cibacron Blue-3 (manufactured by Civer Geigy ■) 7
09/l and Resistol HW8 (manufactured by Kasei Kagaku ■) 80y
/l, soda ash, and sodium alginate were printed in a polka dot pattern, and after steaming at 100℃ for 10 minutes, a water glass of 43° Baumé was picked up with a pick-up rate of 6.
5%, steamed at 100° C. for 1 minute, washed with hot water, washed with water, and dried to obtain a silk-like rayon-silk blended fabric with blue polka dots on an orange background.

かかるレーヨン絹混紡織物の染色諸堅牢変は後記第1表
に示す。
The color fastness changes of such rayon-silk blended fabrics are shown in Table 1 below.

実施例3 綿70M量%と羊毛80重量%の綿、羊毛混紡の、経糸
30番単糸(綿番手)、経糸密度85本/吋、緯糸30
番単糸(綿番手)、緯糸密度70本/吋からなる2/2
の綾組織で日付165y/ゴの綿、羊毛混紡綾織物を製
織した。
Example 3 Cotton and wool blend of 70M% cotton and 80% wool, warp #30 single yarn (cotton count), warp density 85/inch, weft 30
2/2 consisting of count single yarn (cotton count), weft density 70/inch
A cotton and wool blend twill fabric dated 165y/g was woven using the twill weave.

かかる綿、羊毛混紡綾織物を80℃の易で洗った後、酵
素糊抜剤2 f/lを加えて60℃の弓で1時間処理し
、湯洗した後、更にトリポリリン酸ソーダ49/l、精
練漂白用活性剤サンデッド(40−2(三洋化成■製)
2 f/lと過酸化水15 f/lの60℃の水溶液中
で2時間精練、漂白を行い充分湯洗、水洗、脱水、乾燥
した。
After washing the cotton/wool blend twill fabric at 80°C, 2 f/l of enzyme desizing agent was added and treated at 60°C for 1 hour, and after washing with hot water, 49/l of sodium tripolyphosphate was added. Activator for scouring bleaching Sanded (40-2 (manufactured by Sanyo Chemical)
Scouring and bleaching were carried out for 2 hours in an aqueous solution of 2 f/l and peroxide water at 15 f/l at 60°C, followed by sufficient hot water washing, water washing, dehydration, and drying.

得られた織物に実施例2と同様の方法にて地染プリント
処理を行い、得られたプリント物の染色堅牢度を第1表
に示した。
The obtained fabric was subjected to background dyeing printing in the same manner as in Example 2, and the color fastness of the obtained prints is shown in Table 1.

第  −表 尚、測定法は次の通りである。Chapter - Table The measurement method is as follows.

(1)洗堰堅牢度 JIS−L  0844  A2法 (2)耐光堅牢度(1) Washing weir fastness JIS-L 0844 A2 method (2) Light fastness

Claims (11)

【特許請求の範囲】[Claims] (1)セルロース系繊維と蛋白質系繊維とよりなる繊維
構造物に、ビニルスルホン型反応性染料を含有する中性
乃至酸性の染液を付与した後、所定時間放置し、次いで
モノクロロトリアジン型反応性染料とアルカリ剤とビニ
ルスルホン型反応性染料用防染剤とを含有する捺染糊で
印捺し、乾燥、蒸熱処理後、更にアルカリ溶液を付与し
て蒸熱処理することを特徴とする繊維構造物の防染方法
(1) After applying a neutral to acidic dye solution containing a vinyl sulfone type reactive dye to a fiber structure consisting of cellulose fibers and protein fibers, leave it for a predetermined period of time, and then apply a monochlorotriazine type reactive dye. A fibrous structure characterized in that it is printed with a printing paste containing a dye, an alkaline agent, and a resist dye for vinylsulfone type reactive dyes, dried and steamed, and then further coated with an alkaline solution and steamed. Resistance method.
(2)セルロース系繊維が綿、レーヨン、麻である特許
請求の範囲第1項記載の方法。
(2) The method according to claim 1, wherein the cellulose fiber is cotton, rayon, or hemp.
(3)蛋白質系繊維が羊毛又は絹である特許請求の範囲
第1項記載の方法。
(3) The method according to claim 1, wherein the protein fiber is wool or silk.
(4)繊維構造物がセルロース系繊維55〜90重量%
と蛋白質系繊維10〜45重量%とよりなる特許請求の
範囲第1項記載の方法。
(4) The fiber structure is 55 to 90% by weight of cellulose fibers
and 10 to 45% by weight of protein fiber.
(5)染液をパディングにより付与する特許請求の範囲
第1項記載の方法。
(5) The method according to claim 1, wherein the dye liquor is applied by padding.
(6)放置時の温度が10〜60℃である特許請求の範
囲第1項記載の方法。
(6) The method according to claim 1, wherein the temperature during standing is 10 to 60°C.
(7)放置時間が10〜50時間である特許請求の範囲
第1項記載の方法。
(7) The method according to claim 1, wherein the standing time is 10 to 50 hours.
(8)乾燥を80℃以上で行う特許請求の範囲第1項記
載の方法。
(8) The method according to claim 1, wherein the drying is carried out at 80°C or higher.
(9)防染剤が有機スルホン酸塩である特許請求の範囲
第1項記載の方法。
(9) The method according to claim 1, wherein the resist dye is an organic sulfonate.
(10)アルカリ溶液が40〜43度ボーメの水ガラス
溶液である特許請求の範囲第1項記載の方法。
(10) The method according to claim 1, wherein the alkaline solution is a water glass solution having a temperature of 40 to 43 degrees Baumé.
(11)アルカリ溶液付与後の蒸熱処理を少くとも10
0℃で行う特許請求の範囲第1項記載の方法。
(11) Steaming treatment after applying the alkaline solution for at least 10 minutes
The method according to claim 1, which is carried out at 0°C.
JP60185458A 1985-08-22 1985-08-22 Resist style of fiber structure Granted JPS6245793A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60185458A JPS6245793A (en) 1985-08-22 1985-08-22 Resist style of fiber structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60185458A JPS6245793A (en) 1985-08-22 1985-08-22 Resist style of fiber structure

Publications (2)

Publication Number Publication Date
JPS6245793A true JPS6245793A (en) 1987-02-27
JPH0258396B2 JPH0258396B2 (en) 1990-12-07

Family

ID=16171140

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60185458A Granted JPS6245793A (en) 1985-08-22 1985-08-22 Resist style of fiber structure

Country Status (1)

Country Link
JP (1) JPS6245793A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5479336A (en) * 1992-08-06 1995-12-26 Mitsubishi Denki Kabushiki Kaisha DC power-supply unit
US7349300B2 (en) 2003-05-08 2008-03-25 Teac Corporation Optical disk apparatus having variable reproduction speed function

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5479336A (en) * 1992-08-06 1995-12-26 Mitsubishi Denki Kabushiki Kaisha DC power-supply unit
US7349300B2 (en) 2003-05-08 2008-03-25 Teac Corporation Optical disk apparatus having variable reproduction speed function

Also Published As

Publication number Publication date
JPH0258396B2 (en) 1990-12-07

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