Preparation method of catalyst for co-generating of isopropanol and diisobutyl ketone through acetone hydrogenation and application
A diisobutyl ketone and catalyst technology, applied in the field of catalysis, can solve the problems of easy loss and high cost, and achieve the effects of suitable acid strength, stable performance, good activity and selectivity
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Embodiment 1
[0026] Prepare catalyst of the present invention
[0027] Mix 200g of alumina and 4g of methyl cellulose for 30 minutes, add 170mL of 3wt% dilute nitric acid solution, mix for 20 minutes, roll the ball in a granulator to form a 3mm ball, dry at 120°C for 12 hours, and bake at 500°C for 4 hours. Prepare the alumina carrier; then dissolve 110g of magnesium nitrate and 305g of nickel nitrate in deionized water to make 800mL of clarified solution, impregnate the alumina carrier, after 12 hours of immersion, filter out the excess filtrate, and the filtrate is for subsequent use. Drying at ℃ for 12 hours, roasting at 450℃ for 3 hours to obtain a semi-finished catalyst; impregnating the semi-finished catalyst in the filtrate again, repeating the series of impregnation, drying, and roasting three times, drying at 120 °C for 12 hours after each dipping, and roasting at 450 °C for 3 hours Hours, the finished catalyst is finally obtained.
[0028] The catalyst number prepared above is A, ...
Embodiment 2~6
[0031] Other catalysts B to F were prepared according to the method of Example 1, except that the calcination temperature of the carrier and the concentration of the metal salt in the impregnation solution were changed. The catalyst preparation conditions and component contents are shown in Table 1.
[0032] Table 1
[0033] example Catalyst number Nickel content, wt% Magnesium content, wt% Carrier calcination temperature, ℃ Carrier roasting time, hours Calcination temperature after impregnation with metal salt, °C Baking time after impregnating nickel nitrate, ℃ 2 B 21.8 8.6 480 3 380 3 3 C 24.6 9.9 450 6 350 3 4 D 22.9 10.2 550 5 450 4 5 E 22.2 11.5 550 5 420 5 6 F 23.5 9.1 580 4 400 6
[0034] Catalysts B~F were loaded into a fixed-bed reactor and reduced in a hydrogen flow. After reduction, the hydrogenation performance of the catalyst was evaluated under selected reaction conditions. The te...
Embodiment 7
[0041] Activity evaluation experiment
[0042] 100 mL of Catalyst A was loaded into a 100 mL fixed-bed reactor respectively, and technical grade acetone was used as raw material, and the acetone content was 98 wt%. The catalyst is first subjected to reduction treatment, the reduction condition is pressure 0.5MPa, temperature 320°C, time 8 hours, reduction atmosphere is H 2 / N 2 The mixed gas, the hydrogen content is 20.0v%, the flow rate of the reducing gas is 200mL / h; after the reduction, the acetone raw material is passed into the hydrogenation reaction, the total reaction pressure is 3.0MPa, the temperature is 180°C, and the liquid-hour volume of the acetone feed Airspeed 0.8h -1 , The volume ratio of hydrogen and acetone is 200, and a long-term operation test of 2000 hours is carried out.
[0043] The test results show that the conversion rate of acetone and the yield of products isopropanol and DIBK are kept very stable, and the activity of the catalyst does not decrea...
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