Method for preparing hydrodeoxygenation and hydroisomerization catalysts for biological aviation kerosene from camelina oil
A deoxidation catalyst and catalyst technology, applied in the direction of catalyst activation/preparation, organic compound/hydride/coordination complex catalyst, physical/chemical process catalyst, etc., can solve problems affecting catalyst life, etc.
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Embodiment 1
[0033] Embodiment 1. The preparation of hydrodeoxygenation catalyst comprises the following steps:
[0034] (1) Carrier pretreatment: Add 5g of SBA-15 carrier to 15g of 10% tetrabutyl titanate ethanol solution, stir at 80°C for at least 24h, then filter and separate the obtained mixture , then the resulting filter cake was dried in an air atmosphere at 120°C, then roasted at 600°C in an air atmosphere for at least 4h, then cooled to room temperature, and then the obtained sample was added to 15g of citric acid with a mass fraction of 5%. in an aqueous solution, then stirred at 80°C for at least 24 hours, then suction-filtered and separated the obtained mixture, and then dried the obtained filter cake at 120°C to obtain carrier A;
[0035] (2) Loading of active components: Dissolve 7.5g of nickel nitrate, 0.5g of polyethylene glycol 200 and 1.5g of cobalt nitrate in 15g of deionized water under stirring at 80°C, stir well for 5 hours and add to sample A , stirred for at least ...
Embodiment 2
[0036] Embodiment 2. The preparation of hydrodeoxygenation catalyst comprises the following steps:
[0037] (1) Pretreatment of the carrier: Add 5g of SBA-15 carrier to 15g of tetrabutyl titanate ethanol solution with a mass fraction of 15%, stir at 50-70°C for at least 24h, and then suction-filter the resulting mixture , separated, and then the resulting filter cake was dried in an air atmosphere at 120°C, then roasted at 600°C in an air atmosphere for at least 4h, then cooled to room temperature, and then the obtained sample was added to 15g of lemons with a mass fraction of 5%. acid aqueous solution, then stirred at 80°C for at least 24h, then suction-filtered and separated the obtained mixture, and then dried the obtained filter cake at 120°C to obtain carrier B;
[0038] (2) Loading of active components: Dissolve 7.5g of nickel nitrate, 0.5g of polyethylene glycol 200 and 0.49g of ammonium molybdate into 15g of deionized water under stirring at 80°C, stir well for 5 hours...
Embodiment 3
[0039] Embodiment 3. The preparation of hydroisomerization catalyst comprises the following steps:
[0040] (1) The preparation method of multi-level channel SAPO-11: Mix 15g deionized water, 0.72g silica sol, 2.07g phosphoric acid and 1.28g pseudo-boehmite and stir evenly, then add 0.1g starch for hydrolysis reaction and Stir for 5 hours, then add 0.54g of di-n-propylamine and 0.36g of diisopropylamine and stir for another 3 hours; then put the mixture into the microwave synthesis reaction chamber, the microwave frequency is 2.45GHz, the power is set to 250W, and the pressure is set to 250Psi, The synthesis temperature was 200°C, kept for 0.5 hours, then the solid product was taken out and washed, dried at 120°C for 12 hours, and then calcined in a muffle furnace at 600°C for 12 hours to obtain multi-level porous SAPO-11, which is the carrier D;
[0041] (2) Loading of active components: Dissolve 0.13g of chloroplatinic acid and 0.5g of polyethylene glycol into 30g of deioniz...
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