Preparation method of D2 structure hexafluoropropylene dimer
A technology of hexafluoropropylene dimer and hexafluoropropylene, which is applied in the field of chemical technology, can solve the problems of high degree of dissociation and easy aggregation of fluoride anions, and achieve the effect of improving overall performance, reducing the degree of dissociation, and realizing dispersion
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[0042] Catalyst Preparation Example 1
[0043] (1) 5 g of 3-mercaptoic acid, 3 g of vinyl boric acid, 3G vinyl boric acid, adding 2 g of sodium ethanol, stirred to 50 ° C, and the pressure is 0.8 MPa, and the reaction is 100 min, and the reaction is 100 min, resulting in 100 min Additive A;
[0044] (2) The aid A and 25 g of fluorinated potassium fluoride were then mixed for 10 hours, and the molar ratio of the auxiliary agent A and potassium fluoride was 1: 1, and the acetonitrile was evaporated to obtain an isomerization catalyst 1.
Example
[0045] Catalyst Preparation Example 2
[0046] (1) 12 g of 3-mercaptopopyridine, 6 g of vinyl boric acid, 6 g of acetonitrile, 6 g of acetonitrile, and 6 g of sodium ethanol, stirred to 65 ° C, and the pressure is 2.0 MPa, resulting in 150 min Additive A;
[0047] (2) The aid A and 36 g of potassium fluorinated potassium fluoride were subsequently mixed for 20 hours, and the molar ratio of the auxiliary agent A and potassium fluoride was 1: 1.5, and the acetonitrile was evaporated to obtain an isomerization catalyst 2.
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[0048] Example 1
[0049] (1) gather react
[0050] Corium fluoride, calcined by 400 ° C for 10 h, after polishing into a powder, together with anhydrous acetonitrile, mixed with anhydrous acetonitrile, stir mix well, bubble 5 min, then empty, stirring argon circulation 3 times, in vacuum Under the conditions, 20 g of hexafluoropropylene was charged, the control temperature was 30 ° C, the pressure was 0.8 MPa, stirred for 2 h, stirring the rotation speed of 50 r / min, and the reaction was 50 ° C after completing the reaction, then the residual hexafluoropropylene gas was discharged. The liquid is obtained by the lower liquid; in the high pressure reactor;
[0051] (2) isomerization reaction
[0052] 0.5 g of isomerization catalyst 1 was added to the high pressure reactor, and the nitrogen gas was hit by temperature to 100 ° C, and the reaction was 60 min, and the reaction was cooled to room temperature. Propylene dimer.
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