Production method of epoxy propane
A technology of propylene oxide and a production method, applied in the direction of organic chemistry and the like, can solve the problems of decreased effective utilization rate, high separation energy consumption, poor catalyst stability, etc., and achieves improved effective utilization rate, reduced separation energy consumption, and improved stability. Effect
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Embodiment 1
[0010] For the preparation of the catalyst, refer to the literature J.Mol.Catal.A, 2001, 166:219.
[0011] Take by weighing 10.0 grams of tungstic acid and add to 40 milliliters of 30 (weight)% H 2 o 2 In an aqueous solution, stir and heat to 60°C for 60 minutes to obtain a colorless transparent solution. To this solution was added 2.45 ml of aqueous phosphoric acid (40 ml of phosphoric acid in 100 ml of aqueous phosphoric acid), diluted with 80 ml of distilled water and stirring was continued for 30 minutes. 6.9 grams of cetyltrimethylammonium chloride and 3.0 grams of octadecyltrimethylammonium chloride are dissolved in the mixed solution of 160 milliliters of ethylene dichloride, dropwise in the above-mentioned solution rapidly, and continue to stir for 60 A precipitate was formed in 10 minutes, and the precipitate was washed with distilled water until the pH value of the filtrate was about 4, and the filter cake was placed in a rotary evaporator, and vacuum-dried at 60°C...
Embodiment 2
[0013] Adding 120 milliliters of toluene in a 500 milliliter tank reactor is a solvent, then adding 8.0 grams of 60.0 (weight)% H 2 o 2 , 0.45 gram of the catalyst synthesized in [Example 1], and feed 20 gram of chemical grade propylene, and reacted for 8 hours at 55° C. and 1.6 MPa conditions. The reaction results are shown in Table 1.
Embodiment 3
[0015] Adding 120 milliliters of cumene in a 500 milliliter tank reactor is a solvent, then adding 7 grams of 70.0 (weight)% H 2 o 2 , 0.5 gram of the catalyst synthesized in [Example 1], and feed 15 gram of polymer grade propylene, and reacted for 6 hours at 50°C and 1.7MPa conditions, the reaction results are shown in Table 1.
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