A kind of supported heteropolyacid catalyst and preparation method thereof
A heteropolyacid and catalyst technology, applied in the field of supported heteropolyacid catalyst and its preparation, can solve the problems of high equipment requirements, poor low-temperature activity, low initial temperature, etc., and achieve high low-temperature reaction activity and specific surface area The effect of increasing the concentration of reactants
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Embodiment 1
[0041] (1) Catalyst preparation
[0042] Weigh 600g of ammonium phosphate and dissolve it in 2000mL of deionized water to obtain solution A; grind 1000g of petroleum coke to powder, then add it to solution A, leave it for 1.5h, and then filter, the obtained solid sample is placed in an oven at 110°C Dry for 5h. The above-mentioned dried solid samples were pretreated with water vapor at 200 °C for 3 h (the volumetric space velocity of the water vapor gas was 1200 h). -1 ), then the temperature was raised to 400 °C, continued to be pretreated for 3 h, and then cooled to 60 °C under nitrogen protection to obtain pretreated petroleum coke.
[0043] 1000g of the above-obtained pretreated petroleum coke, 38.5g of lanthanum nitrate and 2000g of potassium hydroxide were mixed uniformly, placed in a microwave oven with a microwave frequency of 2450MHz, evacuated, and heated to 500 under the condition that the microwave power was 0.3kw. ℃, kept constant for 40min, then passed nitrogen...
Embodiment 2
[0049] (1) Catalyst preparation
[0050] Weigh 500 g of diammonium hydrogen phosphate, dissolve it in 2000 mL of deionized water to obtain solution A; grind 1000 g of petroleum coke to powder, then add it to solution A, leave it for 1.5 hours, and then filter, and the obtained solid sample is placed in an oven at 110 Dry at ℃ for 5h. The dried solid samples were pretreated with water vapor for 3h at 200°C (the volumetric space velocity of water vapor was 1000h). -1 ), then the temperature was raised to 400 °C, continued to be pretreated for 3 h, and then cooled to 60 °C under nitrogen protection to obtain pretreated petroleum coke.
[0051] 1000g of the above-obtained pretreated petroleum coke, 62.2g of lanthanum nitrate and 3000g of potassium hydroxide were mixed uniformly, placed in a microwave oven with a microwave frequency of 2450MHz, evacuated, and heated to 600 under the condition that the microwave power was 0.3kw. ℃, kept constant for 20min, then passed nitrogen to ...
Embodiment 3
[0057] (1) Catalyst preparation
[0058] Weigh 400 g of ammonium dihydrogen phosphate and dissolve it in 2000 mL of deionized water to obtain solution A; grind 1000 g of petroleum coke to powder, then add it to solution A, leave it for 1.5 hours, and then filter, and the obtained solid sample is placed in an oven at 110 Dry at ℃ for 5h. The dried solid samples were pretreated with water vapor for 3h at 200°C (the volumetric space velocity of water vapor was 800h). -1 ), then the temperature was raised to 400 °C, continued to be pretreated for 3 h, and then cooled to 60 °C under nitrogen protection to obtain pretreated petroleum coke.
[0059] 1000g of the above-obtained pretreated petroleum coke, 89.9g of lanthanum nitrate and 4000g of potassium hydroxide were mixed uniformly, placed in a microwave oven with a microwave frequency of 2450MHz, evacuated, and heated to 400 under the condition that the microwave power was 0.3kw. ℃, kept constant for 60min, then passed nitrogen t...
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