Preparation method of vulcanized hydrocracking catalyst
A hydrocracking and catalyst technology, which is applied in the direction of catalyst activation/preparation, organic compound/hydride/coordination complex catalyst, physical/chemical process catalyst, etc., can solve the problem of not being fully vulcanized, affecting catalyst performance, and influencing factors Many problems, to achieve the effect of good application prospects, shortened start-up time, high yield of diesel oil
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Embodiment 1
[0034] Weigh 200 g of pseudo-boehmite (dry basis, unless otherwise specified, all weights of the following raw materials are dry basis), 170 g of amorphous silica-alumina, and 30 g of USY molecular sieve, and fully mix these three solid powders Finally, 300 mL of pre-prepared dilute nitric acid solution was added to it, kneaded for 15 minutes, extruded through a 3.0 mm orifice plate, dried at 140 °C for 12 h, and then calcined at 560 °C for 4 h in an air atmosphere to obtain the catalyst carrier Z0.
Embodiment 2
[0036] Weigh 5.8g of 3-mercaptopropyltriethoxysilane and add it into 100mL of 95% ethanol solution, stir at room temperature for 20min to fully dissolve it. Then 40 g of the carrier Z0 prepared in Example 1 was added to the above solution, allowed to stand at room temperature for 12 hours, then heated to 70° C., and then reacted for 4 hours. After the reaction, pour out the excess ethanol solution, wash the obtained solid particles with absolute ethanol at room temperature for 3 times, then dry them at 70°C for 1 hour in an air atmosphere, and then put them into a vacuum drying oven at 70°C to fully dry to obtain the surface-modified carrier Z1 .
Embodiment 3
[0038] Weigh 5.6g of 3-aminopropyltriethoxysilane and add it into 100mL of 95% ethanol solution, stir at room temperature for 20min to fully dissolve it. Then, 40 g of the carrier Z0 prepared in Example 1 was added to the above solution, and the reaction vessel was purged with nitrogen and kept under a slight positive pressure in the nitrogen atmosphere. The reaction was left at room temperature for 12 hours, then heated to 60° C., and then reacted for 4 hours. After the reaction, pour out the excess ethanol solution, wash the obtained solid particles with absolute ethanol at room temperature for 3 times, and then pre-dry them at room temperature for 4 hours in an air atmosphere, and then put them into a vacuum drying oven to fully dry at 70 °C to obtain a surface-modified carrier Z2.
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