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Fatty acid monoethanolamide succinate sulfonate and preparation method and application thereof

A technology of monoethanolamine and boric acid amide salt, which is applied to the preparation of sulfonate, chemical instruments and methods, transportation and packaging, etc., can solve the problems of workpiece cleaning and other problems, and achieve good cooling performance, good lubricity, and good biodegradability Effect

Active Publication Date: 2016-01-13
深圳市泓丰科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] In recent years, the research on micro-cutting technology has made great progress, which has reduced the harm to the environment caused by the discharge of a large amount of cutting oil, but there is still a problem of cleaning the processed workpiece

Method used

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  • Fatty acid monoethanolamide succinate sulfonate and preparation method and application thereof
  • Fatty acid monoethanolamide succinate sulfonate and preparation method and application thereof
  • Fatty acid monoethanolamide succinate sulfonate and preparation method and application thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0055]Step 1. Put 282.47kg (1000mol) of oleic acid and 61.08kg (1000mol) of monoethanolamine into the reactor respectively, while stirring and raising the temperature to 90°C. After 1 hour of reaction, oleic acid monoethanolamide is obtained.

[0056] Step 2: Add the oleic acid monoethanolamide and 58.04kg (500mol) maleic acid generated in step 1 into the reactor, add 8kg of cation exchange resin, fill in nitrogen to convert the air in the reactor to react, and the reaction temperature is : 200°C; Reaction time: 4 hours; After the reaction, the water is decompressed and the cation exchange resin is removed, which is oleic acid monoethanolamide maleate.

[0057] Step 3: Fully stir the oleic acid monoethanolamide maleate and the aqueous solution containing 120.17 kg (1000 mol) of potassium bisulfite produced in the reaction of step 2, and react to remove water to generate oleic acid monoethanolamide succinate sulfonate Potassium acid.

Embodiment 2

[0059] Step 1. Put 144.20 kg (1000 mol) of isooctanoic acid and 61.08 kg (1000 mol) of monoethanolamine into the reaction kettle, stir at the same time and raise the temperature to 70 ° C. After 2 hours of reaction, it is isooctanoic acid monoethanolamide.

[0060] Step 2: Add the isooctanoic acid monoethanolamide ether and 49.03kg (500mol) maleic anhydride generated in step 1 into the reaction kettle, and add H 2 SO 4 Sulfuric acid 1.25kg aqueous solution, filled with nitrogen to convert the air in the reactor to react, the reaction temperature is: 180 ° C; the reaction time is: 5 hours; after the reaction, part of the water is decompressed and neutralized by adding potassium hydroxide to a pH of 8 ~8.5, that is, isooctanoic acid monoethanolamide maleate.

[0061] Step 3: Fully stir the isooctanoic acid monoethanolamide maleate and the aqueous solution containing 104.06 kg (1000 mol) of sodium bisulfite formed in the reaction of step 2 to react and remove the water to genera...

Embodiment 3

[0063] Step 1. Put 284.48kg (1000mol) of stearic acid and 61.08kg (1000mol) of monoethanolamine into the reaction kettle respectively, stir at the same time and raise the temperature to 80°C, and react for 1.5 hours to obtain stearic acid monoethanolamide.

[0064] Step 2: Add the stearic acid monoethanolamide and 58.04kg (500mol) fumaric acid produced in step 1 into the reactor, add 4.036kg of cation exchange resin, fill in nitrogen to convert the air in the reactor for reaction, and react The temperature is: 220°C; the reaction time is: 3 hours; after the reaction, the water is decompressed and the cation exchange resin is removed to obtain stearic acid monoethanolamide fumarate.

[0065] Step 3: Fully stir the stearic acid monoethanolamide fumarate and the aqueous solution containing 120.17 kg (1000 mol) of potassium bisulfite produced by the reaction in step 2 to carry out the reaction, remove the water by reverse osmosis, and generate stearic acid monoethanolamide fumarate...

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Abstract

The invention provides a method for preparing fatty acid monoethanolamide succinate sulfonate, which is characterized in that: fatty acid monoethanolamine is generated by amidation reaction of fatty acid and monoethanolamine, and then reacted with butenedioic acid or butenedioic anhydride to form Fatty acid monoethanolamine succinate, and then react with bisulfite to form a salt of fatty acid monoethanolamine succinate sulfonate. Compared with the prior art, the trace cutting fluid produced by using the fatty acid monoethanolamide succinate sulfonate provided by the invention has good lubricity, extreme pressure anti-wear and biodegradability, and a very small amount of trace Cutting fluid can meet the high-end requirements of metal processing, reduce the harm to the environment and workers, and minimize the pollution to the environment.

Description

technical field [0001] The invention relates to the technical field of synthetic chemistry, in particular to fatty acid monoethanolamide succinate sulfonate and its preparation method and application. Background technique [0002] Cutting oils, coolants, emulsions and other lubricants used in traditional metal processing lubrication and cooling are used in large quantities, and traditional cutting oils use mineral oil as the base oil, which is not easy to decompose in the natural environment, and most of the additives used are harmful to the human body. Harmful to the environment, it not only wastes resources, but also causes huge pollution of processing sites and the environment. [0003] The finished workpiece needs to be cleaned with a large amount of cleaning solvent before processing in the next process, resulting in a large amount of pollutant discharge. At the same time, the cleaning agent often contains chlorides (such as methylene chloride, tetrachloroethylene), pho...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C309/17C07C303/32B01F17/10B01F17/22C10M173/02C10M105/72C10N40/22C10N30/06C10N30/04C10N30/12C09K23/10C09K23/22
Inventor 张乃庆吴启东
Owner 深圳市泓丰科技有限公司
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