A kind of dual active group yellow reactive dye that can be used for printing

A reactive dye and dual-reactive technology, applied in the field of dual-reactive base yellow reactive dyes, can solve the problems of inability to meet the preparation of mother liquor in automatic sizing system, failure to save cost and reduce consumption, and generate more sewage, and achieve bright color and fastness. Excellent degree of indicators, the effect of eliminating waste water

Active Publication Date: 2020-04-03
无锡润新染料有限公司
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] Traditional reactive yellow dyes, such as Brilliant Yellow K-6G, although the production and sales volume is large, still have some shortcomings, mainly as follows: low strength, cannot be used for printing and dyeing extra-dark colors, and cannot meet the mother liquor preparation of automatic pulping system
At the same time, in order to meet the vividness of the color, salting-out purification is carried out before commercialization, which produces a lot of sewage and high production costs. This method has failed to meet the requirements of cost-saving and clean production.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0017] A double reactive yellow reactive dye that can be used for printing is characterized in that it is composed of compound I and compound II, wherein the molar ratio of compound I and compound II is 14~16: 2~3;

[0018] The preparation method of compound I is: first condense cyanuric chloride and 2,4 diaminobenzenesulfonic acid for the first time, then add 3.5 diaminobenzoic acid in the first condensation, carry out the second condensation, and the second After the secondary condensation, under the action of hydrochloric acid and sodium nitrite, carry out diazotization reaction to generate diazonium salt, and finally add N-ethylpyridone to the diazonium salt for alkaline coupling, concentrate and spray dry to obtain ;

[0019] The preparation method of compound II is as follows: first condense cyanuric chloride and 2,4 diaminobenzenesulfonic acid for the first time, then add m-(β-sulfate ethyl sulfone) aniline in the first condensation, and carry out the second condensatio...

Embodiment 2

[0021] The preparation method of compound I: first condense cyanuric chloride and 2,4 diaminobenzenesulfonic acid for the first time, then add 3.5 diaminobenzoic acid in the first condensation, carry out the second condensation, the second After the condensation, under the action of hydrochloric acid and sodium nitrite, carry out diazotization reaction to generate diazonium salt, and finally add N-ethylpyridone to the diazonium salt for alkaline coupling, concentrate and spray dry to obtain the compound Component I; wherein, cyanuric chloride and 2,4 diaminobenzenesulfonic acid are condensed for the first time, the temperature is carried out at -5°C~10°C, the pH value is 1~3, and three in the first condensation reaction The molar ratio of polycyanogen chloride to 2,4 diaminobenzenesulfonic acid is 1:0.9~1.1; 3.5 diaminobenzoic acid is added to the first condensation, and the second condensation is carried out at a temperature of 20°C~30°C Carry out, PH value 4~6 carry out, rea...

Embodiment 3

[0023] The preparation method of compound II: first condense cyanuric chloride and 2,4 diaminobenzenesulfonic acid for the first time, then add m-(β-sulfate ethyl sulfone) aniline in the first condensation, and carry out the second After the second condensation, after the second condensation, under the action of hydrochloric acid and sodium nitrite, carry out diazotization reaction to produce diazonium salt, and finally add N-ethylpyridone methylsulfonate to the diazonium salt to carry out Alkaline coupling, concentrated and sprayed to dry to obtain the compound II component; among them, the first condensation of cyanuric chloride and 2,4 diaminobenzenesulfonic acid is carried out at a temperature of -5°C to 10°C, and the pH value is 1~3, the molar ratio of cyanuric chloride and 2,4 diaminobenzenesulfonic acid in the first condensation reaction is 1:0.9~1.1; The second condensation is carried out at a temperature of 30°C to 3.40°C, a pH value of 6 to 7, and a reaction time of ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
solubility (mass)aaaaaaaaaa
solubility (mass)aaaaaaaaaa
color fastnessaaaaaaaaaa
Login to view more

Abstract

The invention discloses double-reactive-group yellow active dye which can be applied to printing. The double-reactive-group yellow active dye comprises a composition I and a composition II, wherein the molar ratio of the composition I to the composition II is (14-16):(2-3), and both of the composition I and composition II are obtained by performing multiple condensation and coupling on cyanuric chloride and 2,4-diaminobenzenesulfonic acid. Through the double-reactive-group yellow active dye, not only can wastewater brought by salting out in a traditional process be avoided, but also the colorof the dye can be brighter through compounding; and the fastness index is more superior, the solubility reaches 160 g / L at 25 DEG C, the light fastness reaches a sixth grade, the colorfastness to soaping reaches a fourth grade, the rub fastness reaches a fourth-fifth grade, and the sweat fastness reaches a fourth-fifth grade.

Description

technical field [0001] The invention belongs to the field of chemical printing and dyeing, and in particular relates to a yellow reactive dye with double active groups that can be used for printing. Background technique [0002] Traditional reactive yellow dyes, such as Brilliant Yellow K-6G, have large production and sales volume, but still have some shortcomings, mainly as follows: low strength, cannot be used for printing and dyeing extra-dark colors, and cannot meet the mother liquor preparation of automatic pulping system. At the same time, in order to meet the vividness of the color, salting-out purification is carried out before commercialization, which produces a lot of sewage and high production costs. This method has failed to meet the requirements of cost-saving and clean production. Contents of the invention [0003] Purpose of the invention: the purpose of the present invention is to provide a kind of double reactive yellow reactive dye that can be used for pr...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): C07D251/50C07D251/00C09B62/085C09B62/51C09B67/22C09B67/24
CPCC09B62/085C09B62/51C09B67/004C09B67/0047C09B67/0072
Inventor 周佳易任争艳秦超
Owner 无锡润新染料有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products