Unlock instant, AI-driven research and patent intelligence for your innovation.

Ester group-containing quaternary ammonium salt compound and its application

A quaternary ammonium salt compound and compound technology, which is applied in the field of ester group-containing compounds, can solve the problems of poor pigment stability, reduced pigment tinting strength, and complicated preparation process, and achieve good storage stability, enhanced transparency, and low preparation costs. low effect

Active Publication Date: 2019-10-29
LILY GRP CO LTD +1
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

If an anionic surfactant is used to disperse the pigment, desorption is easy to occur, and the stability of the treated pigment is not good; when an organic substance containing an aromatic ring is used as a dispersant, the coloring power of the pigment will be more or less reduced when the pigment is treated; and When using pigment derivatives to disperse pigments, although the performance is superior, the preparation process is complicated and the cost is high

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
  • Ester group-containing quaternary ammonium salt compound and its application
  • Ester group-containing quaternary ammonium salt compound and its application
  • Ester group-containing quaternary ammonium salt compound and its application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] The preparation of the Gemini quaternary ammonium salt containing ester group as shown in structure:

[0041]

[0042] (1) Put 1 part of 2,3-butanediol, 2.5 parts of chloroacetic acid and 2 parts of anhydrous sodium sulfate into the reactor, and add p-toluenesulfonic acid (1% of the mass of the reactant). Under the protection of nitrogen, the mixture was heated to 120° C., cooled to room temperature after reacting for 6 hours, and the water agent, anhydrous sodium sulfate, was removed by suction filtration. The organic layer was washed with saturated NaHCO 3 Wash with aqueous and deionized water until the pH is neutral. The solvent was removed under reduced pressure to give 2,3-butanediol chloroacetate.

[0043] (2) Add 1 part of 2,3-butanediol chloroacetate and 2.5 parts of N,N-dimethyldodecyl tertiary amine prepared above into the reactor, and then add an appropriate amount of dichloromethane as Solvent, reflux at 90-100°C for 10 hours to obtain a Gemini quatern...

Embodiment 2

[0046] The preparation of the Gemini quaternary ammonium salt containing ester group as shown in structure:

[0047]

[0048] (1) Put 1 part of ethylene glycol, 2.5 parts of chloroacetic acid and 2 parts of anhydrous sodium sulfate into the reactor, and add p-toluenesulfonic acid (1% of the mass of the reactant). Under the protection of nitrogen, the mixture was heated to 120° C., cooled to room temperature after reacting for 6 hours, and the water agent, anhydrous sodium sulfate, was removed by suction filtration. The organic layer was washed with saturated NaHCO 3 Wash with aqueous and deionized water until the pH is neutral. The solvent was removed under reduced pressure to give ethylene glycol chloroacetate.

[0049] (2) 1 part of ethylene glycol chloroacetate and 2.5 parts of N,N-dimethyl dodecyl tertiary amine prepared above are added to the reactor, and then an appropriate amount of dichloromethane is added as a solvent, at 90 Reflux at ~100°C for 10 hours to obta...

Embodiment 3

[0052] The preparation of the Gemini quaternary ammonium salt that contains ester group as shown in structure:

[0053]

[0054] (1) Put 1 part of ethylene glycol, 2.5 parts of chloroacetic acid and 2 parts of anhydrous sodium sulfate into the reactor, and add p-toluenesulfonic acid (1% of the mass of the reactant). Under the protection of nitrogen, the mixture was heated to 120° C., cooled to room temperature after reacting for 6 hours, and the water agent, anhydrous sodium sulfate, was removed by suction filtration. The organic layer was washed with saturated NaHCO3 Wash with aqueous and deionized water until the pH is neutral. The solvent was removed under reduced pressure to give ethylene glycol chloroacetate.

[0055] (2) Add 1 part of ethylene glycol chloroacetate and 2.5 parts of N,N-dimethyloctadecyl tertiary amine prepared above into the reactor, then add an appropriate amount of dichloromethane as solvent, at 90 Reflux at ~100°C for 10 hours to obtain a Gemini q...

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 relates to the field of organic pigments, and concretely relates to an ester group-containing quaternary ammonium salt compound and a use thereof. The quaternary ammonium salt compound has a structure represented by formula (1); and in the formula (1), R is H and one selected from C1-C5 alkyl groups, m is 11 to 17, n is 1 to 5, and X is halogen. The quaternary ammonium salt compound designed and prepared in the invention can be used as an organic pigment dispersant to make pigment particles become smaller, have enhanced transparence and greatly improved color. The pigment has improved glossiness, has a green phase migrating hue, and keeps a good storage stability.

Description

technical field [0001] The invention relates to the technical field of organic pigments, in particular to an ester group-containing compound and its application. Background technique [0002] During the preparation process of most organic pigments, the initial crystal nuclei become single crystals, and the single crystals will further grow into primary particles, and then form well-crystallized primary particles through the process of crystallization and maturation. Due to the extremely high surface energy of the generated primary particles, it is easy to form secondary particles (0.1μ~20μ) and difficult to disperse, so that the application of organic pigments (such as in coatings or inks, the particle size of organic pigments cannot be greater than 0.15μ) into trouble. The close accumulation of primary particles is called coagulated particles; the loose accumulation of primary particles is called aggregated particles; the further aggregation or flocculation of aggregated p...

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): C07C227/04C07C229/12C09B67/36C09D11/03
CPCC07C67/08C07C227/04C09B67/0079C09D11/03C07C229/12C07C69/63
Inventor 王利民梁丽王桂峰王峰韩建伟田禾陈立荣黄卓
Owner LILY GRP CO LTD