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High-performance double-chromophoric-body brilliant blue reactive dye and preparation method thereof

A technology of reactive dyes and blue dyes, which is applied in the field of high-performance dichroic brilliant blue reactive dyes and its preparation, and can solve the problems of directness, exhaustion rate, inconsistent reactivity, etc.

Active Publication Date: 2021-04-20
江苏德美科化工有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] The technical problem to be solved in the present invention is to provide a kind of high-performance dichroic brilliant blue reactive dye and its preparation method. In the reactive blue dye, there are two chromophoric absorption wavelengths with different structures that can be effectively superimposed, and the two All the color bodies do not contain heavy metal ions, which greatly improves the environmental protection of reactive blue dyes in this application, and overcomes the inconsistencies of directness, exhaustion rate, reactivity, etc. in the intermolecular color matching of existing reactive blue dyes Question, reactive blue dye not only has high lifting power, but also has excellent light fastness properties

Method used

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  • High-performance double-chromophoric-body brilliant blue reactive dye and preparation method thereof
  • High-performance double-chromophoric-body brilliant blue reactive dye and preparation method thereof
  • High-performance double-chromophoric-body brilliant blue reactive dye and preparation method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0048] Such as figure 1 shown as figure 1 Shown a kind of high-performance dichromatic brilliant blue reactive dye and preparation method thereof,

[0049]

[0050] In the above formula I, X is F or Cl; M is -H or an alkali metal; R 1 , R 4 -H or -CH 3 ; 2 , R 3 for -H or -SO 3 H;

[0051] In this example, R in the general structural formula I 1 , R 4 -H or -CH 3 ; 2 , R 3 for -H or -SO 3 H; X is Cl; M is Na.

[0052] In this embodiment, in the general structural formula I, R 1 , R 2 , R 4 For -H, R 3 for-SO 3 H; R 1 , R 3 , R 4 for -CH 3 when R 2 for-SO 3 H; X is Cl; M is Na.

[0053] In this embodiment, the commercial dyeing agent includes 75% by mass of reactive blue dye, 5% by mass of diffusing agent, 0.1% by mass of dustproof agent, and 5% by mass of sodium sulfate .

[0054] In this embodiment, the diffusing agent is methylnaphthalenesulfonic acid formaldehyde condensate, and the dustproof agent is a water-soluble polymer compound.

[0055]...

Embodiment 2

[0068] The difference between this embodiment and embodiment 1 is:

[0069] In this embodiment, the commercial dyeing agent includes 85% by mass of reactive blue dye, 15% by mass of diffusing agent, 0.5% by mass of dustproof agent, and 15% by mass of sodium sulfate ;

[0070] In this embodiment, the molar ratio of 4-aminodiphenylamine-2-sulfonic acid to sodium nitrite is 1:1.01; the molar ratio of 4-aminodiphenylamine-2-sulfonic acid to hydrochloric acid is 1:2.5;

[0071] In this embodiment, the molar ratio of 4-aminodiphenylamine-2-sulfonic acid diazonium salt to H acid is 1:1;

[0072] In this embodiment, the molar ratio of cyanuric chloride or cyanuric fluoride to the monoazo dye of H acid is 1:1;

[0073] In this embodiment, the blue chromophore a1 obtained by the reaction of bromic acid and M acid in the preparation step (4) is replaced by the blue chromophore a1 obtained by the reaction of bromic acid and metabis;

[0074] In this embodiment, the molar ratio of the b...

Embodiment 3

[0076] The difference between this embodiment and embodiment 1 is:

[0077] In this embodiment, the commercial dyeing agent includes 85% by mass of reactive blue dye, 15% by mass of diffusing agent, 0.5% by mass of dustproof agent, and 15% by mass of sodium sulfate .

[0078] In this embodiment, the molar ratio of 4-aminodiphenylamine-2-sulfonic acid to sodium nitrite is 1:1.03; the molar ratio of 4-aminodiphenylamine-2-sulfonic acid to hydrochloric acid is 1:2.8;

[0079] In this embodiment, the molar ratio of 4-aminodiphenylamine-2-sulfonic acid diazonium salt to H acid is 0.98:1;

[0080] In this embodiment, the molar ratio of cyanuric chloride or cyanuric fluoride to the monoazo dye of H acid is 1.03:1;

[0081] In this embodiment, the molar ratio of the blue color group a1 of the anthraquinone chromophore to the condensation product of cyanuric chloride or cyanuric fluoride is 1.03:1.

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Abstract

The invention discloses a high-performance double-chromophoric-body brilliant blue reactive dye and a preparation method thereof, and belongs to the technical field of reactive dyes, the reactive dye comprises a general formula (I), and X is F or Cl; M is-H or alkali metal; R1 and the R4 are-H or-CH3; R2 and R3 are-H or-SO3H, and X is Cl; M is Na; In the structural general formula (I), when R1, R2 and R4 are-H, R3 is-SO3H; when R1, R3 and R4 are-CH3, R2 is-SO3H; X is Cl; and M is Na. The absorption wavelengths of the two chromophoric bodies with different structures in the reactive blue dye can be effectively superposed, the synergistic hyperchromic effect of the two chromophoric bodies is greatly improved, the bright degree of the dye color is improved, the two chromophoric bodies do not contain heavy metal ions, the environmental protection property of the reactive blue dye is greatly improved, and the application prospect is wide. Meanwhile, the problems of inconsistency of directness, dye exhaustion rate, reactivity and the like during intermolecular color matching of the existing reactive blue dye are solved, and the reactive blue dye has high lifting power.

Description

technical field [0001] The invention relates to the technical field of reactive dyes, in particular to a high-performance dichroic brilliant blue reactive dye and a preparation method thereof. Background technique [0002] Reactive dyes are rich in variety and bright in color, and their molecular structure contains reactive groups, which can chemically react with hydroxyl groups on cellulose fibers and amino groups on protein fibers, and combine with fibers through covalent bonds. Therefore, the fastness performance of the dyed fiber is superior. At present, most reactive dyes on the market are usually single-chromosome reactive dyes such as reactive yellow FG (C.I. reactive yellow 42), reactive orange KN-2G (C.I. reactive orange 72), reactive red 5-B (C.I. reactive red 35 ), P-6GS Bright Yellow (C.I. Reactive Yellow 95), P-3R Brilliant Blue (C.I. Reactive Blue 49), etc. [0003] In addition to single-chromosome reactive dyes, when a single dye molecular structure contains...

Claims

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Application Information

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IPC IPC(8): C09B62/085C09B67/24C09B67/36C09B67/04B02C15/00B02C23/00D06P1/382D06P3/66
Inventor 杨晶晶陈赛龙王小军周建新
Owner 江苏德美科化工有限公司
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