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Sodium fatty acyloxy isopropyl sulfonate and its synthesis method and application

A fatty acyloxyisopropyl sulfonate sodium, fatty acid technology, applied in the sulfonate preparation, chemical instruments and methods, surface active non-soap compounds and washing compositions and other directions, can solve fatty acyloxyisopropyl sulfonic acid Sodium is not sold commercially, and the formula is not reported, etc., to achieve the effects of excellent water solubility, easy industrial production, and simple synthesis process

Active Publication Date: 2016-06-22
CHINA RES INST OF DAILY CHEM IND
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Fatty acyloxy isopropyl sodium sulfonate is as the modified product of fatty acyloxy ethyl sulfonate sodium, and its synthesis process has not been reported both at home and abroad, especially the intermediate sodium hydroxypropyl sulfonate has no commercially available product, and needs its own Preparation; Simultaneously because sodium fatty acyloxy isopropyl sulfonate is not sold commercially, so its related formula has not been reported yet

Method used

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  • Sodium fatty acyloxy isopropyl sulfonate and its synthesis method and application
  • Sodium fatty acyloxy isopropyl sulfonate and its synthesis method and application
  • Sodium fatty acyloxy isopropyl sulfonate and its synthesis method and application

Examples

Experimental program
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Effect test

Embodiment 1

[0025] Add 52g of sodium bisulfite, 0.08g of ethylenediaminetetraacetic acid and 80g of water into a closed reaction kettle, stir for 10 minutes to dissolve, then slowly press 38g of propylene oxide into the kettle with nitrogen gas, raise the temperature to 70°C, and seal it. Reaction 0.5hr, the maximum pressure in the process can reach 3atm, the pressure is almost zero when the reaction is complete, the residual amount of sodium bisulfite is 0.03%, and the active substance is 165g of sodium hydroxypropyl sulfonate aqueous solution with 50.4% of the output, which is directly used in The next step is esterification.

[0026] In the four-necked flask that stirrer, thermometer, long-necked dropping funnel, reflux condenser and water separator are equipped with, add coconut oil 100g, 50.4% sodium hydroxypropyl sulfonate 135g, catalyst zinc oxide 0.4g, Carry out mixing preheating, after treating that coconut oil all melts, control stirring speed to be 200rpm, gradually heat up and...

Embodiment 2

[0030] Add 52g of sodium bisulfite, 0.16g of maleic acid and 80g of water into a closed reaction kettle, stir for 10 minutes to dissolve, then slowly press 32g of propylene oxide into the kettle with nitrogen, raise the temperature to 60°C, and conduct a closed reaction for 1.5 hr, the maximum pressure in the process can reach 2.6atm, the pressure is almost zero when the reaction is complete, the residual amount of sodium bisulfite is 0.016%, and the active substance is 160g of 51.8% sodium hydroxypropyl sulfonate aqueous solution obtained from the discharge, which is directly used for the following One-step esterification reaction.

[0031] In a four-necked flask equipped with a stirrer, a thermometer, a long-necked dropping funnel, a reflux condenser and a water separator, add 100 g of lauric acid, 115 g of 51.8% sodium hydroxypropyl sulfonate, and 0.2 g of catalyst zinc oxide, and carry out Mix and preheat. After the lauric acid is completely melted, control the stirring sp...

Embodiment 3

[0035] Add 52g of sodium bisulfite, 0.14g of succinic acid and 80g of water into a closed reaction kettle, stir for 10 minutes to dissolve, then slowly press 32g of propylene oxide into the kettle with nitrogen gas, raise the temperature to 50°C, and react in a closed reaction for 2 hours. The maximum pressure in the process can reach 1 atm, and the pressure is almost zero when the reaction is complete. The residual amount of sodium bisulfite is 0.008%, and 160g of sodium hydroxypropyl sulfonate aqueous solution with an active substance of 48.6% is obtained from the discharge, which is directly used in the next step of esterification reaction.

[0036] In the four-neck flask equipped with agitator, thermometer, long-necked dropping funnel, reflux condenser and water separator, add stearic acid 142g, 48.6% sodium hydroxypropyl sulfonate 125g, catalyst zinc oxide 0.6g, Carry out mixing preheating, after stearic acid is all melted, control agitation speed to be 400rpm, heat up gr...

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Abstract

The structural formula of a kind of fatty acyloxy isopropyl sodium sulfonate is: where R is C 7 ~C 17 Saturated or unsaturated straight-chain hydrocarbon groups. The invention has the advantages of greatly reducing the Krafft point below 1°C, excellent water solubility, good foam performance, strong hard water resistance, strong detergency, wider application range, simple synthesis process and easy industrial production.

Description

technical field [0001] The invention belongs to a synthesis method and application of a surfactant, in particular to a synthesis method and application of fatty acyloxyisopropyl sodium sulfonate. Background technique [0002] Traditional soaps are highly alkaline and have obvious irritating effects on the skin. They are not resistant to hard water, have strong degreasing ability, and dry skin after washing, so neutral soaps came into being. The pH value of the neutral soap is close to 7, which is milder to the skin, and the skin is moisturized and smooth after use. The main component of neutral soap is sodium fatty acyloxyethyl sulfonate (common name: Igepon A, Igepon A), which has good surface activity, excellent wetting power, detergency, hard water resistance and calcium Soap dispersing ability, widely used in personal care products, dishwashing detergent, metal cleaning agent, leather cleaning agent, blanket cleaning agent and other products. Although sodium fatty acyl...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C309/12C07C303/32C11D10/04A61Q19/10A61Q19/00
Inventor 李运玲宋永波李秋小智丽飞侯素珍
Owner CHINA RES INST OF DAILY CHEM IND