A kind of preparation method of polypentaerythritol fatty acid ester
A technology of alcohol octaerythritol fatty acid ester and pentaerythritol, which is applied in the field of preparation of polypentaerythritol fatty acid ester, and achieves the effects of good synergy, excellent thermal stability, and low cost
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Embodiment 1
[0033] The synthesis of dipentaerythritol myristate comprises the following steps:
[0034] S1. Add myristic acid and pyridine into a four-neck flask equipped with a reflux condenser, a stirrer, a thermometer and an air guide tube in a mass ratio of 1:5, and stir at a speed of 350r / min;
[0035] S2. Pass nitrogen into the mixture of S1, then according to the ratio of fatty acid: dipentaerythritol=1:10, at a speed of 20 drops / min, drop dipentaerythritol into the mixture at a constant speed with a constant pressure funnel, in the solid superacid catalyst S 2 o 8 2- / ZrO 2 -TiO 2 -Al 2 o 3 Under the action of the esterification reaction, the esterification reaction is carried out under the reaction conditions of about 240 ° C, and the reaction end point is judged by measuring the pH value (acidity) and the water output;
[0036] S3. The product obtained in S2 was evaporated to remove pyridine under reduced pressure, decolorized, and filtered to obtain dipentaerythritol myri...
Embodiment 2
[0038] The synthesis of dipentaerythritol 2-ethylbutyrate comprises the following steps:
[0039] S1. Add 2-ethylbutyric acid and xylene into a four-neck flask equipped with a reflux condenser, a stirrer, a thermometer and an air guide tube according to a mass ratio of 1:7, and stir at a speed of 550r / min;
[0040] S2. Feed nitrogen into the mixture of S1, then according to the ratio of fatty acid: dipentaerythritol=1:1, at a speed of 6 drops / min, drop dipentaerythritol into the mixture at a constant speed with a constant pressure funnel, in the solid superacid catalyst S 2 o 8 2- / ZrO 2 -TiO 2 -Al 2 o 3 Under the action of the reaction, the esterification reaction is carried out under the reaction conditions of about 200 ° C, and the reaction end point is judged by measuring the pH value (acidity) and the water output;
[0041] S3. The product obtained in S2 was evaporated to remove xylene under reduced pressure, decolorized, and filtered to obtain dipentaerythritol 2-e...
Embodiment 3
[0043] The synthesis of dipentaerythritol octanediol adipate comprises the following steps:
[0044] S1. Add adipic acid into a four-necked flask equipped with a reflux condenser, a stirrer, a thermometer, and an air guide tube. At a speed of 20 drops / min, use a constant pressure funnel to drop 2 times the amount of adipic acid at a constant speed. -Ethyl-1,3-hexanediol, reacted at 60°C for 6h;
[0045] S2. At a speed of 6-20 drops / min, drop the mixture of S1 into a four-necked bottle of thionyl chloride filled with 2 times of adipic acid at a constant speed with a constant pressure funnel, and reflux at 60°C for 10 hours. Obtain adipate bis(acyl chloride) octyl chloride;
[0046] S3. in the product that S2 obtains, add 2 times of the dipentaerythritol of adipic acid, in solid superacid catalyst S2 o 8 2- / ZrO 2 -TiO 2 -Al 2 o 3 Under the action of N-methylpyrrolidone, it was reacted at room temperature for 12 hours, filtered, neutralized with acetic acid capping, and e...
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