JPS63282382A - Dyeing method - Google Patents
Dyeing methodInfo
- Publication number
- JPS63282382A JPS63282382A JP62115994A JP11599487A JPS63282382A JP S63282382 A JPS63282382 A JP S63282382A JP 62115994 A JP62115994 A JP 62115994A JP 11599487 A JP11599487 A JP 11599487A JP S63282382 A JPS63282382 A JP S63282382A
- Authority
- JP
- Japan
- Prior art keywords
- group
- dyeing
- water
- formula
- parts
- 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
Links
- 238000004043 dyeing Methods 0.000 title claims description 31
- 238000000034 method Methods 0.000 title description 22
- 229920000728 polyester Polymers 0.000 claims description 24
- 229920003043 Cellulose fiber Polymers 0.000 claims description 20
- 150000001875 compounds Chemical class 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 17
- 239000000986 disperse dye Substances 0.000 claims description 16
- 239000000835 fiber Substances 0.000 claims description 15
- 125000001174 sulfone group Chemical group 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 238000010186 staining Methods 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- -1 phenyl- Chemical group 0.000 claims description 2
- 238000007447 staining method Methods 0.000 claims description 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- 238000005406 washing Methods 0.000 description 20
- 229920000742 Cotton Polymers 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 238000001035 drying Methods 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000007850 fluorescent dye Substances 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003518 caustics Substances 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000010014 continuous dyeing Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000009980 pad dyeing Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
Landscapes
- Coloring (AREA)
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
本発明は染色法に関する。更に詳しくは特定の構造を有
する化合物(螢光染料)の共存下に行われるポリエステ
ル繊維/セルロール繊維混紡(以下T/C混と略す)の
ポリエステル繊維の染色法に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a dyeing process. More specifically, the present invention relates to a method for dyeing a polyester fiber/cellulose fiber blend (hereinafter abbreviated as T/C blend) in the presence of a compound having a specific structure (fluorescent dye).
従来の技術
T/C混の染色においてはポリエステル線維■側を分散
染料で有色に染色し次いでセルロース線維(q側をセル
ロース線維用染料でやはり有色−に染色する(又、は逆
の順序)というのが通常の方法であるが近年ポリエステ
ル繊維側のみを有色に染色しセルロース繊維側は未染色
のまま(白色)に残したようなT/c混布帛も多(使用
されるようになった。ところで分散染料を用いたT/C
混の染色においては染色操作が終ったのち未染着分散染
料を除く為に還元洗浄、ソーピング、水洗等の後処理を
施すことが不可欠であるがこれらの後処理によって未染
着の分散染料、分散染料の分解等がセルロース線維を汚
染するという問題がある。このような問題点を解決する
ためにセルロース繊維に対する汚染性の小さい分散染料
を用いたり、還元洗浄、ソーピング、水洗等に堅牢な分
散染料を用いる工夫がなされている。又分散染料による
染色時にセルロース繊維用の螢光染料を併用してセルロ
ース繊維側を白(みせるような工夫も行われている。Conventional technology When dyeing T/C blends, the polyester fiber (1) side is dyed colored with a disperse dye, and then the cellulose fiber (q) side is dyed (also colored) with a cellulose fiber dye (or in the reverse order). This is the usual method, but in recent years, many T/c mixed fabrics have been used in which only the polyester fiber side is colored and the cellulose fiber side is left undyed (white). By the way, T/C using disperse dye
In mixed dyeing, it is essential to perform post-treatments such as reduction washing, soaping, and water washing to remove undyed disperse dye after the dyeing operation is completed. There is a problem in that the decomposition of disperse dyes contaminates cellulose fibers. To solve these problems, efforts have been made to use disperse dyes that are less likely to stain cellulose fibers, or to use disperse dyes that are robust to reduction cleaning, soaping, water washing, and the like. Also, when dyeing with disperse dyes, a fluorescent dye for cellulose fibers is used in combination to make the cellulose fibers appear white.
発明が解明しようとする問題点
セルロース線維に対する汚染性の小さい分散染料や還元
洗浄等の後処理に堅牢な分散染料を用いる方法はセルロ
ース繊維を白く残す効果が十分でなく又通常の螢光染料
はテトロン繊維の染色において採用されるような高温条
件下ではセルロース繊維用の螢光染料がセルロース繊維
に対して十分な染着力を示さずその結果とじてセルロー
ス繊維を白く残す効果が十分でないという欠点がある。Problems to be Solved by the Invention Methods that use disperse dyes that have low staining properties on cellulose fibers, or disperse dyes that are robust in post-treatments such as reduction cleaning, do not have a sufficient effect of leaving cellulose fibers white. The disadvantage is that fluorescent dyes for cellulose fibers do not exhibit sufficient dyeing power to cellulose fibers under high-temperature conditions such as those used in dyeing Tetoron fibers, and as a result, the effect of leaving cellulose fibers white is not sufficient. There is.
発明が解決しようとする問題点
本発明者は前記したような問題点を解決すべく鋭意研究
を重ねた結果本発明に至ったものである。即ち本発明は
分散染料によってポリエステル繊維/セルロース繊維混
紡(T/C混)のポリエステル繊維のみを染色するにあ
たり遊離酸として式(1)
(式(1)において几、、R2はそれぞれ独立に低級ア
ルキル基、スルホン基、スルファモイル基、クロル原子
又はカルボキシル基の1乃至2で置換されていてもよい
アニリノ基;スルホン基で置換されていてもよいフェノ
キシ基;ヒドロキシ基、スルホン基又はカルボキシル基
で置換されていてもよいモノ又はジアルキルアミノ基;
フェニル−、メチル−アミノ基;モ空ホリノ基:低級ア
ルコキシ基;アミノ基又はヒドロキシル基を表す)
で示される化合物の共存下に染色を行うことを特徴とす
るT/C混の染色法を提供する。Problems to be Solved by the Invention The present inventor has conducted extensive research to solve the above-mentioned problems, and as a result has arrived at the present invention. That is, in the present invention, when dyeing only polyester fibers of a polyester fiber/cellulose fiber blend (T/C blend) with a disperse dye, the free acid is expressed as the formula (1) (in formula (1), 几, R2 are each independently a lower alkyl Anilino group which may be substituted with 1 or 2 of a group, sulfone group, sulfamoyl group, chloro atom or carboxyl group; Phenoxy group which may be substituted with a sulfone group; Substituted with a hydroxy group, sulfone group or carboxyl group an optional mono- or dialkylamino group;
Provides a T/C mixed dyeing method characterized in that dyeing is carried out in the coexistence of a compound represented by the following: phenyl-, methyl-amino group; movac holino group; lower alkoxy group; represents an amino group or a hydroxyl group. do.
本発明の染色法を詳細に説明する。The staining method of the present invention will be explained in detail.
式(1)で示される化合物は例えば特開昭51−524
46等によりて公知の化合物であるがこれらの化合物は
例えば次のようにして装造される。The compound represented by formula (1) is disclosed in, for example, JP-A-51-524.
46 and the like, and these compounds can be prepared, for example, as follows.
2モルの塩化シアヌルをまずアセトンに溶解しこれを界
面活性剤を含有した氷水中に投入しよく分散させたのち
この分散液に4.4−ジアノスチルベン−2,2−ジス
ルホン゛酸1モルヲ加工p)14〜9、温度0〜3.5
℃で縮合(1火線合)して次の化合物をえる。First, 2 mol of cyanuric chloride was dissolved in acetone, and this was poured into ice water containing a surfactant to disperse it well. Then, 1 mol of 4,4-dianostilbene-2,2-disulfonic acid was added to this dispersion. Processing p) 14-9, temperature 0-3.5
Condensation (single caustic combination) at ℃ yields the following compound.
次いで(2)式の化合物と下記式(3)及び(4)Rl
H(3)
R2−H(4)
(式(3)及び(4)においてR+及び■t2は前記と
同じ意味を表す)
で表される化合物各2モルと任意の順序で縮合反応(2
火線合、3火線合)を行って式(1)の化合物をえる。Next, the compound of formula (2) and the following formulas (3) and (4) Rl
Condensation reaction (2
A compound of formula (1) is obtained by performing a caustic combination and a three-caustic combination.
本発明の方法で染色の対象となる繊維は、ポリエステル
繊維と木綿、レーヨン、麻等のセルロース系繊維との混
紡・交織品であるか混合繊維であってよくその形態は布
状、メリヤス状、糸状等どのような形態であってもよい
。The fiber to be dyed in the method of the present invention may be a blended or interwoven product of polyester fiber and cellulose fiber such as cotton, rayon, hemp, etc., or may be a mixed fiber in the form of cloth, stockinette, etc. It may be in any form such as filamentous.
弐(1)の化合物を共存せしめてT/C混を染色するに
あたってはポリエステル線維を分散染料で染色する方法
即ち浸染法(高温染色法)、キャリアー法、捺染法、パ
ッド染色法等がそのまま適用しうるものである。When dyeing a T/C blend by coexisting the compound in (2) (1), methods for dyeing polyester fibers with disperse dyes, such as dip dyeing method (high temperature dyeing method), carrier method, textile printing method, pad dyeing method, etc., can be applied as is. It is possible.
浸染法においては通常の分散染料と式(1)の化合物及
び必要に応じてノニオン系界面活性剤、アニオン系界面
活性剤、pH調整剤からなる染浴を調製しこれにT/C
混を投入し98〜140℃より好ましくは110〜13
0℃で20〜90分間染色を行う。この場合浴比は通常
l:5〜1:50であり式(1)の化合物はT/C混の
セルロース繊維含有量に対して通常0.01〜5%より
好ましくは1〜3%(重量比)である。染色を終了した
なら常法により水洗、ソーピング、還元洗浄、水洗を行
ってセルロース繊維が白く残されたT/C混染色物をえ
る。In the dyeing method, a dye bath consisting of a normal disperse dye, a compound of formula (1) and, if necessary, a nonionic surfactant, an anionic surfactant, and a pH adjuster is prepared, and then T/C is applied to the dye bath.
98~140℃, preferably 110~13℃
Staining is carried out for 20-90 minutes at 0°C. In this case, the bath ratio is usually 1:5 to 1:50, and the compound of formula (1) is usually 0.01 to 5%, preferably 1 to 3% (by weight) based on the cellulose fiber content of the T/C blend. ratio). After dyeing is completed, water washing, soaping, reduction washing, and water washing are carried out in a conventional manner to obtain a T/C mixed dyed product in which the cellulose fibers remain white.
キャリアー法においては分散染料、式(1)の化合物及
びクロルベンゼン系キャリア等から染浴を調製し常法に
より90〜110 ’Cで0.5〜2時間染色を行い水
洗、還元洗滌、水洗を行いセルロース繊維部が純白に残
されたT/C混の染色物をえる。In the carrier method, a dye bath is prepared from a disperse dye, a compound of formula (1), a chlorobenzene carrier, etc., and dyeing is carried out in a conventional manner at 90 to 110'C for 0.5 to 2 hours, followed by washing with water, reduction washing, and washing with water. A dyed T/C blend is obtained in which the cellulose fibers remain pure white.
更に捺染法、パッド染色法による連続染色法も常法によ
って実施することが出来る。Furthermore, a continuous dyeing method using a textile printing method or a pad dyeing method can also be carried out by conventional methods.
実施例
次に実施例によって本発明を具体的に説明する。実施例
中スルホン基、カルボキシル基は遊離酸の形で表すもの
とし部とあるのは重量部を表すものとする。EXAMPLES Next, the present invention will be specifically explained by examples. In the examples, sulfone groups and carboxyl groups are expressed in the form of free acids, and parts are by weight.
実施例1゜
式(5)
で表される化合物0.05部とカヤロンポリエステルブ
ラックEX−8F200(日本化薬製、分散染料)を1
00部の水に溶解し、酢酸0.01部を加え、ポリエス
テル繊維/木綿混紡品(50150)5部と加えて13
0℃に昇温し、ついで60分染色した染色終了後、水洗
、ソーピンク、還元洗浄後水洗した。Example 1 0.05 part of the compound represented by formula (5) and 1 part of Kayalon Polyester Black EX-8F200 (manufactured by Nippon Kayaku, disperse dye)
Dissolved in 0.00 parts of water, added 0.01 part of acetic acid, added 5 parts of polyester fiber/cotton blend (50150) to 13
The temperature was raised to 0° C., and then dyeing was carried out for 60 minutes. After finishing the dyeing, washing with water, sowing pink, reduction washing, and washing with water were carried out.
得られた染色物はそのポリエステル繊維部が純黒に染色
されているのに対しその木綿繊維部は純白のままであっ
た。In the resulting dyed product, the polyester fiber portion was dyed pure black, while the cotton fiber portion remained pure white.
実施例2〜i o。Example 2-io.
次に示される化合物(螢光染料)を用いて実施例1と同
様にしてT/C混の染色を行い木綿側が純白に残された
T/C混染色物を得た。A T/C mixed dyeing was carried out in the same manner as in Example 1 using the compound (fluorescent dye) shown below to obtain a T/C mixed dyed product in which the cotton side remained pure white.
実施例 Rr Rz
2 −NH@ −NHO
3−o+5o3H−N < CH3)29 −NH(
γC0OH−NH()cooHlo−OCI−13−N
H2
比較例
カヤロンポリエステルブラックEX−8F2000.5
部を100部の水に分散溶解し、酢酸0.01部を加え
、ポリエステル/木綿混紡品(50150)5部と加え
て130℃に昇温し、ついで60分染色した染色終了後
、水洗、ソーピンク、還元洗浄後水洗、乾燥した。Example Rr Rz
2 -NH@ -NHO 3-o+5o3H-N < CH3)29 -NH(
γC0OH-NH()cooHlo-OCI-13-N
H2 Comparative example Kayalon polyester black EX-8F2000.5
1 part was dispersed and dissolved in 100 parts of water, 0.01 part of acetic acid was added, 5 parts of polyester/cotton blend (50150) was added, the temperature was raised to 130°C, and then dyed for 60 minutes. After the dyeing was completed, washed with water, So pink, after reduction cleaning, washing with water and drying.
得られた染色物は、木綿繊維部が黄汚味に変色していた
。In the obtained dyed product, the cotton fiber portion was discolored to a yellowish tinge.
実施例11. 浸染(キャリヤー法)式
で表される化合物0.05部とカヤロンポリエステルブ
ラックEX−8F200(日本化薬裂、分散染料)を1
00部の水に溶解し、酢酸0.01部とキャリヤー剤(
日華化学裂、テトロシンK)0.5部を加え、ポリエス
テル/レーヨン交織品(50150)5部を加えて10
0℃に昇温しついで60分染色した。染色終了後、水洗
、ソーピング、還元洗浄後、水洗、乾燥した。Example 11. Dyeing (carrier method) 0.05 part of a compound expressed by the formula and 1 part of Kayalon Polyester Black EX-8F200 (Nippon Kayakusaki, disperse dye)
Dissolved in 0.00 parts of water, 0.01 part of acetic acid and carrier agent (
Add 0.5 parts of Nikka Kagaku Setsu, Tetrosin K) and 5 parts of polyester/rayon mixed fabric (50150) to make 10
The temperature was raised to 0°C and dyeing was carried out for 60 minutes. After dyeing, it was washed with water, soaped, reduced, washed with water, and dried.
得られた染色物はレーヨン側の白変が著しく優°れてい
た。The resulting dyed product had remarkable white discoloration on the rayon side.
実施例12.捺染法
式
で表される化合物 0.1部カヤロ
ンポリエステルブラックEX−8F 200 5
部元 糊 PBL−600(安達糊料裂)
60 部塩素酸ソーダ
0.5部酒石酸 0.2部
インプルバー880(横浜ポリマー製) 2 部
微温湯 32.2部
合 計 100 部上記
色糊をポリエステル/木綿交織品にスクリーンを用いて
印捺し、中間乾燥を行い、続いて170°CX7分の加
熱処理を行った。Example 12. Compound expressed by printing method 0.1 part Kayalon Polyester Black EX-8F 200 5
Part glue PBL-600 (Adachi paste)
60 parts Sodium chlorate
0.5 parts Tartaric acid 0.2 parts Implebar 880 (manufactured by Yokohama Polymer) 2 parts lukewarm water 32.2 parts Total 100 parts The above color paste was printed on a polyester/cotton woven product using a screen, intermediate drying was performed, and then Heat treatment was performed at 170° C. for 7 minutes.
水洗、ソーピング、還元洗浄、水洗、乾燥した。Washing with water, soaping, reduction washing, washing with water, and drying.
得られた染色物は木綿側の白変が著しく浸れていた。The resulting dyed product had significant white discoloration on the cotton side.
実施例13.連続染色法
式
で表される化合物 0.1部カヤロ
ンポリエステルブラックEX−8F200 5
部アルギン酸ソーダ
0.1部微温湯 94.8部
合 計 100 部上記パッ
ド液をポリエステル/木綿交織品にパッドし、100℃
×3分の中間乾燥を行い、続いて200℃x90秒の加
熱処理を行い、水洗、ソーピング、還元洗浄、水洗、乾
燥した。Example 13. Compound expressed by continuous dyeing method 0.1 part Kayalon Polyester Black EX-8F200 5
Sodium alginate
0.1 part lukewarm water 94.8 parts Total 100 parts Pad the above padding solution onto a polyester/cotton woven product and heat at 100°C.
Intermediate drying was performed for 3 minutes, followed by heat treatment at 200° C. for 90 seconds, washing with water, soaping, reduction washing, washing with water, and drying.
得られた染色物は木綿側の白変が著しく優れていた。The resulting dyed product had remarkable white discoloration on the cotton side.
実施例14゜
カヤロンポリエステルブラックEX−8Fの原末30部
と次式
で示される化合物2部をデモールN(花王社製、分散剤
)40部とデモールC(花王社製、分散剤)28部とで
湿潤状態にて、5時間微粒子化処理をしたのち、乾燥し
微粒子化物を得た。この微粒子混合物0.50部を10
0部の水忙分散溶解し、酢酸0.01部を加え、ポリエ
ステル/木綿混紡品(50150)5部を加えて130
℃に昇温し、ついで60分染色した染色終了後、水洗、
ソーピング、還元洗浄後水洗した。Example 14 30 parts of bulk powder of Kayalon Polyester Black EX-8F and 2 parts of the compound represented by the following formula were mixed with 40 parts of Demol N (manufactured by Kao Corporation, dispersant) and 28 parts of Demol C (manufactured by Kao Corporation, dispersant). The mixture was subjected to micronization treatment for 5 hours in a wet state, and then dried to obtain a micronized product. 10 parts of this fine particle mixture
Dissolve 0 parts in water, add 0.01 part of acetic acid, and add 5 parts of polyester/cotton blend (50150) to make 130 parts.
The temperature was raised to ℃ and then dyed for 60 minutes.After dyeing, washing with water,
After soaping and reduction cleaning, it was washed with water.
木綿側が純白に残されたポリエステル/木綿混紡品の染
色物かえられた。The dyeing of the polyester/cotton blend was changed, leaving the cotton side pure white.
発明の効果
T/C混の染色においてセルロース繊維を白残ししてポ
リエステル繊維のみを有色に染色するに当り白残し効果
のすぐれた染色法が確立された。Effects of the Invention In dyeing T/C blends, a dyeing method has been established that leaves cellulose fibers white and dyes only polyester fibers colored, with an excellent white leaving effect.
Claims (1)
維混紡(T/C混)のポリエステル繊維のみを染色する
にあたり遊離酸として式(1)▲数式、化学式、表等が
あります▼(1) (式(1)においてR_1、R_2はそれぞれ独立に低
級アルキル基、スルホン基、スルファモイル基、クロル
原子又はカルボキシル基の1乃至2で置換されていても
よいアニリノ基;スルホン基で置換されていてもよいフ
ェノキシ基;ヒドロキシ基、スルホン基又はカルボキシ
ル基で置換されていてもよいモノ又はジアルキルアミノ
基;フエニル−、メチル−アミノ基;モルホリノ基;低
級アルコキシ基;アミノ基又はヒドロキシル基を表す) で示される化合物の共存下に染色を行うことを特徴とす
るT/C混の染色法[Claims] 1. When dyeing only polyester fibers of polyester fiber/cellulose fiber blend (T/C blend) with disperse dye, there are formula (1) ▲ mathematical formula, chemical formula, table, etc. ▼ (1 ) (In formula (1), R_1 and R_2 are each independently an anilino group which may be substituted with 1 or 2 of a lower alkyl group, a sulfone group, a sulfamoyl group, a chloro atom or a carboxyl group; a phenoxy group which may be substituted with a hydroxy group, a sulfone group or a carboxyl group; a phenyl-, methyl-amino group; a morpholino group; a lower alkoxy group; an amino group or a hydroxyl group) A T/C mixed staining method characterized by staining in the coexistence of the indicated compound
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62115994A JPS63282382A (en) | 1987-05-14 | 1987-05-14 | Dyeing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62115994A JPS63282382A (en) | 1987-05-14 | 1987-05-14 | Dyeing method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63282382A true JPS63282382A (en) | 1988-11-18 |
Family
ID=14676222
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62115994A Pending JPS63282382A (en) | 1987-05-14 | 1987-05-14 | Dyeing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63282382A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998042685A1 (en) * | 1997-03-25 | 1998-10-01 | Ciba Specialty Chemicals Holding Inc. | Fluorescent whitening agents |
US5873913A (en) * | 1994-06-23 | 1999-02-23 | Clariant Finance (Bvi) Limited | Optical brightening agents |
US6426382B1 (en) | 1998-06-22 | 2002-07-30 | Clariant Finance (Bvi) Limited | Polycationic polymer salts, their production and use |
KR100511154B1 (en) * | 1996-12-24 | 2006-02-17 | 시바 스페셜티 케미칼스 홀딩 인크. | Bis-triazinylamino-stilbene, cleaning cycle fabric softener concentrate composition containing the same, and method for improving UV protection index of textile products using the same |
CN105113285A (en) * | 2015-09-19 | 2015-12-02 | 苏州大学 | Slurry disperse dye and preparation method and appliance |
-
1987
- 1987-05-14 JP JP62115994A patent/JPS63282382A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5873913A (en) * | 1994-06-23 | 1999-02-23 | Clariant Finance (Bvi) Limited | Optical brightening agents |
KR100511154B1 (en) * | 1996-12-24 | 2006-02-17 | 시바 스페셜티 케미칼스 홀딩 인크. | Bis-triazinylamino-stilbene, cleaning cycle fabric softener concentrate composition containing the same, and method for improving UV protection index of textile products using the same |
WO1998042685A1 (en) * | 1997-03-25 | 1998-10-01 | Ciba Specialty Chemicals Holding Inc. | Fluorescent whitening agents |
EP1123929A1 (en) * | 1997-03-25 | 2001-08-16 | Ciba SC Holding AG | Fluorescent whitening agents |
US6458169B2 (en) * | 1997-03-25 | 2002-10-01 | Ciba Specialty Chemicals Corporation | Fluorescent whitening agents |
US6464735B2 (en) * | 1997-03-25 | 2002-10-15 | Ciba Specialty Chemicals Corporation | Fluorescent whitening agents |
US6426382B1 (en) | 1998-06-22 | 2002-07-30 | Clariant Finance (Bvi) Limited | Polycationic polymer salts, their production and use |
CN105113285A (en) * | 2015-09-19 | 2015-12-02 | 苏州大学 | Slurry disperse dye and preparation method and appliance |
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