High-light-fastness emerald reactive dye compound and application thereof

A reactive dye and emerald green technology, applied in the direction of reactive dyes, azo dyes, organic dyes, etc., can solve the problems of poor diffusion performance, solubility difference, poor compatibility, etc., achieve excellent light fastness performance, improve daylight Effects of light fastness, good development potential

Inactive Publication Date: 2018-03-06
上海俪源科技有限公司
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, green dyes are mostly prepared by compounding two or three kinds of dyes, but due to the differences in the solubility of compound dyes, directness to fibers during dyeing, reactivity to alkali fixation and other performance differences, resulting in poor dyeing stability, Easy to dye flowers, large color difference between front and back
For example, reactive blue phthalocyanine structure dyes, whose mo

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

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • High-light-fastness emerald reactive dye compound and application thereof
  • High-light-fastness emerald reactive dye compound and application thereof
  • High-light-fastness emerald reactive dye compound and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] This embodiment provides a kind of emerald green reactive dye compound with high sun exposure, which is specifically prepared by the following method:

[0025] (a) Chlorosulfonation reaction: at 40°C, slowly (within half an hour) add 0.100mol of copper phthalocyanine powder to 220mL of chlorosulfonic acid, stir for 30min, then raise the temperature to 135-140°C, maintain the reaction for 3h; cool down to 80°C, and dropwise added 0.504mol thionyl chloride within 2h, then raised the temperature to 90°C, and kept the temperature for 2h; after the reaction was completed, it was lowered to room temperature, poured into ice water while stirring, and precipitated; stood still, filtered, The filter cake was washed with ice water until neutral to obtain the copper phthalocyaninesulfonyl chloride filter cake, which was set aside;

[0026] (b) Primary condensation reaction: 0.101mol cyanuric chloride and 60g crushed ice were beaten for 30 minutes at 0°C; 0.100mol 2,4-diaminobenzen...

Embodiment 2

[0032] This example provides a high-sun emerald green reactive dye compound, the specific preparation method of which is similar to that of Example 1. The difference is: N-methyl-3-formamido-4-methyl-6-hydroxyl-2-pyridone in step (d) is replaced by N-ethyl-3-formamido-4-methyl -6-hydroxyl-2-pyridone, consumption is 0.100mol; Through step (f), finally obtain a kind of emerald green reactive dye compound containing copper phthalocyanine and pyridone double color body, structure such as the formula in table 1 (I-2A).

Embodiment 3

[0034] This example provides a high-sun emerald green reactive dye compound, the specific preparation method of which is similar to that of Example 1. The difference is: N-methyl-3-formamido-4-methyl-6-hydroxyl-2-pyridone in step (d) is replaced by 1-(4'-sulfonic acid phenyl)-3- Methyl-5-pyrazolone, consumption is 0.100mol, is dissolved in 150mL water, and with 20% sodium carbonate solution adjustment pH value is 7~8, and pH value is maintained at 7~8 in the reaction process; Through step (f) , and finally obtain an emerald green reactive dye compound containing copper phthalocyanine and pyrazolone dichromate, the structure of which is shown in the formula (I-3A) in Table 1.

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

No PUM Login to view more

Abstract

The invention provides a high-light-fastness emerald reactive dye compound, which has the following general structural formula (I), a+b+c=3.5, wherein CuPc, X, R1, R2 and R3 are as defined in the specification. The high-light-fastness emerald reactive dye compound can directly realize intramolecular color matching through yellow and blue double-chromophore in molecules, thus thoroughly solving a series of problems during dye compounding. In addition, the emerald reactive dye compound has excellent light fastness and good application effect, and has a good development prospect in clothing and/or other textile, especially in curtain and auto interior materials.

Description

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

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
Owner 上海俪源科技有限公司
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2023 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap