Method of synthesizing a fluorine-containing demoulding additive with agricultural processing side product cardanol
A release additive and agricultural processing technology, applied in additives, petroleum industry, lubricating composition, etc., can solve the problems of high-efficiency fluorine release agent dependence on imports, etc., to improve release efficiency and product processing quality, sufficient source of raw materials, Effects that meet high-end needs
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Embodiment 2
[0031] In a four-neck flask equipped with a stirring device, a reflux condensing device, and a thermometer, add 100 mL of acetone, 30 g of cardanol, and 51 g of hexafluoropropylene oxide oligomer, start stirring, and slowly add 2.0 g of N,N-dimethyl Hexylcyclohexylamine, kept in an oil bath at a temperature of 20°C to 30°C, after a nucleophilic substitution reaction for 8 to 9 hours, the acetone was evaporated to obtain a fluorine-containing mixed phenol product substituted by a hexafluoropropylene oxide oligomer , and then add 2 grams of sulfuric acid to the four-necked bottle, heat up to 85°C to 95°C and keep it for 1 to 2 hours, then add 9.6 grams of 2-valeric acid, 1.5 grams of p-benzoquinone and 1.0 grams of methane to the four-necked bottle Sulfonic acid, continue to heat up to 175 ° C ~ 185 ° C for 8 hours, lower the temperature, dilute the reactant with dilute sodium hydroxide solution, filter, take the filtrate, and generate the product, add 25 grams of monoethanolamin...
Embodiment 3
[0033]In a four-necked flask equipped with a stirring device, a reflux condensing device and a thermometer, add 100 mL of acetone, 35 g of cardanol and 54 g of hexafluoropropylene oxide oligomer, start stirring, and slowly add 1.5 g of N-ethylmorpholine , kept in an oil bath at a temperature of 25°C to 35°C, carried out a nucleophilic substitution reaction for 7 to 8 hours, then distilled off the acetone to obtain a fluorine-containing mixed phenol product substituted by a hexafluoropropylene oxide oligomer, and then added to four Add 3 grams of sulfuric acid into the bottle, heat up to 85°C-95°C and keep it for 1-2 hours, then add 9.8 grams of trans-crotonic acid, 2.0 grams of p-benzoquinone and 1.4 grams of methanesulfonic acid into the four-necked bottle, Continue to raise the temperature to 185°C to 195°C to react for 7 hours, lower the temperature, dilute the reactant with dilute sodium hydroxide solution, filter, take the filtrate, and generate the product, add 26 grams o...
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