Synthesis method for imidazoline ampholytic surfactant

A technology of surfactant and synthesis method, applied in chemical instruments and methods, dissolution, organic chemistry, etc., can solve the problems of high energy consumption, difficult recycling, easy oxidation of amines, etc.

Inactive Publication Date: 2017-06-13
TIANJIN POLYTECHNIC UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

"Normal pressure heating dehydration method" requires high temperature, long reaction time, and incomplete dehydration, amine is easy to oxidize, and consumes a lot of energy; although "vacuum heating dehydration method" makes the reaction proceed at a lower temperature, it can prevent Oxidation of air, but requires high sealing performance of the equipment, and the degree of vacuum is not easy to control. It is easy to extract the amine and discharge it to produce diamide; although the "solvent dehydration method" has stable water output and the amine is not easy to be taken out, it will increase the cost. Consumes a certain amount of latent solvent, and the use of latent solvent will also cause a certain degree of pollution and is not easy to recycle

Method used

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  • Synthesis method for imidazoline ampholytic surfactant
  • Synthesis method for imidazoline ampholytic surfactant

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0013] The synthetic method of embodiment 1. imidazoline laurate amphoteric surfactant

[0014] Step 1: in the 500mL four-necked flask that magnetic stirring, thermometer and decompression distillation device are housed, add a certain amount of lauric acid and diethylenetriamine, make the mol ratio of lauric acid and diethylenetriamine be 1: 1.2, Under nitrogen protection, start heating and stir slowly. When the temperature is around 44°C, lauric acid begins to melt. When the temperature rises to about 72°C, lauric acid and diethylenetriamine are completely mixed, and then the reaction temperature is raised to 130°C. At about ℃, water vapor began to appear on the bottle wall at this time. Start the vacuum pump to adjust the vacuum degree of the reaction system to 0.07MPa, and continue to heat up. When the temperature is 140℃, the first drop of water appears in the receiver, and the reaction continues to form water. When the temperature rises to 160°C, the water outlet speed be...

Embodiment 2

[0016] The synthetic method of embodiment 2. imidazoline stearic acid amphoteric surfactant

[0017] Step 1: In the 500mL four-neck flask that magnetic stirring, thermometer and vacuum distillation device are housed, add a certain amount of stearic acid and hydroxyethylethylenediamine, make the mole of stearic acid and hydroxyethylethylenediamine The ratio is 1:1.2, nitrogen protection, start heating and stirring slowly, when the reaction temperature rises to about 130°C, water vapor begins to appear on the bottle wall at this time, start the vacuum pump to adjust the vacuum degree of the reaction system at 0.08MPa, continue to heat up, When the temperature is 140°C, the first drop of water appears in the receiver, and the reaction continues to form water. When the temperature rises to 160°C, the water outlet speed becomes slower, and almost no water is formed. The reaction time at this stage is about 2 hours. Continue to heat up. When the temperature is about 200°C, the amoun...

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Abstract

The invention relates to a synthesis technique for a surfactant. The synthesis technique is mainly suitable for synthesizing an imidazoline derivative, especially an amine (hydroxyl) ethyl alkyl imidazoline ampholytic surfactant. The synthesis technique includes the following synthesis steps that fatty acid and polyamine are added into a four-opening flask according to the molar ratio of 1:(1-1.3), the temperature is raised to 140-220 DEG C, the vacuum degree is 0.05 MPa to 0.09 MPa, the reaction is carried out for 4 h to 7 h, and an imidazoline intermediate is synthesized; the end point of the reaction is determined by measuring the acid value and the actual water outflow amount; the synthesized imidazoline intermediate and sodium chloroacetate are subjected to quaternarization according to the molar ratio of 1:(1-3), the temperature of 75-95 DEG C, the time of 3 h-5 h, the pH range of 7-9 and the solid content of 30%-50%, and the imidazoline ampholytic surfactant is synthesized.

Description

technical field [0001] The invention relates to a synthesis technology of surfactants, which is mainly suitable for synthesizing imidazoline derivatives, especially amine (hydroxy) ethyl alkyl imidazoline amphoteric surfactants. Background technique [0002] Imidazoline amphoteric surfactants have low toxicity, no irritation, softness, antistatic properties, compatibility with anion, cation, and nonionic surfactants, biodegradability, wetting, foaming, emulsification, and dispersibility, etc. Excellent performance, widely used in cleaning agent, cosmetics, textile industry, antistatic agent and metal processing, etc. [0003] Imidazoline intermediates are important monomers for the synthesis of imidazoline amphoteric surfactants, and the quality of imidazoline intermediates is related to the smooth synthesis of imidazoline amphoteric surfactants. The main step of synthesizing imidazoline intermediates is to remove the water generated in the reaction. Generally, "normal pres...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D233/26B01F17/32C09K23/32
CPCC07D233/26C09K23/00
Inventor 郑帼焦晓芳孙玉刘燕军徐进云周存吴波朱佳文
Owner TIANJIN POLYTECHNIC UNIV
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