Method for extracting isostearic acid from mono acid
A technology of isostearic acid and monoacid, which is applied in the field of extracting isostearic acid from monoacid, can solve the problems of low separation efficiency and product impact, and achieve simple extraction method, low toxicity, and cheap and easy-to-obtain raw materials Effect
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Embodiment 1
[0031] Add 3kg of urea and 7kg of absolute ethanol into a reaction kettle with a stirrer and a reflux condenser, heat it in a water bath to 68°C under the conditions of stirring and reflux to dissolve the urea and obtain a clear solution, add 1kg of clay to catalyze oleic acid, Continue to stir and reflux for 30 minutes to stop the reaction. After cooling the reactant to room temperature, put it in a refrigerator at 10° C. and perform cold analysis for 15 hours. Suction filter the reactant after cold analysis to obtain white fatty acid-urea inclusion complex and light yellow filtrate. The inclusion complex can be dissolved in water to recover urea and obtain linear stearic acid. The filtrate contains solvent and isostearic acid Acids are therefore separated and collected.
[0032] Distill the filtrate under reduced pressure at a pressure of 0.09Mpa and a temperature of 37°C to remove absolute ethanol, and the recovery rate of the solvent can reach 80%. Wash with hot water at ...
Embodiment 2
[0034] The solvent in Example 1 was replaced with 8 kg of 95% ethanol aqueous solution, and the rest of the extraction steps were the same as in Example 1. As a result, 303 g of isostearic acid was obtained, with a yield of 30.3%, and the recovery rate was the theoretical content of isostearic acid in the monoacid of 84.4%. After determination, the acid value of the product is 177.4mgKOH / g, and the saponification value is 182.4mgKOH / g.
Embodiment 3
[0036] Add 3kg of urea and 6kg of 95% methanol aqueous solution into a reaction kettle with a stirrer and a reflux condenser, heat it in a water bath to 68°C under the condition of stirring and reflux, the urea dissolves quickly and forms a clear solution, add 1kg of linoleic acid After producing the by-products of dimer acid, continue to stir and reflux for 30 minutes to stop the reaction. After cooling the reactant to room temperature, put it in a refrigerator at 10° C. for 15 hours of cold analysis. The reactant after suction filtration and cold analysis was obtained white fatty acid-urea inclusion complex and light yellow filtrate. The filtrate was distilled under reduced pressure at a pressure of 0.10 MPa and a temperature of 45° C. to remove the solvent. Wash with hot water at 90°C and dry in a constant temperature oven at 40°C to obtain 342g of isostearic acid product with a yield of 34.2%. The recovery rate is the theory of isostearic acid in the by-product of linoleic...
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