Preparation method for hydrocracking catalyst
A hydrocracking and catalyst technology, applied in physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve problems such as unstable properties of heteropolyacids and insufficient catalyst stability
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Embodiment 1
[0038] The carrier T-1 of Comparative Example 1 was impregnated with an impregnation solution containing tungsten and nickel at room temperature for 2 hours, and dried at 120°C for 4 hours to prepare a solution of ammonium dihydrogen phosphate with a concentration of 30% by weight. The material was impregnated with the prepared phosphorus-containing solution for 2 hours, dried at 120°C for 4 hours, heat-treated at 250°C for 6 hours in an air atmosphere, and then reduced and activated in a hydrogen atmosphere. The reduction and activation procedure was 5°C / min from room temperature Raise to 450°C at a rate of 2°C / min, from 450°C to 700°C, and keep the temperature at 700°C for 2 hours to prepare the catalyst C-1 of the present invention.
Embodiment 2
[0043] The carrier T-2 of Comparative Example 2 was impregnated with an impregnation solution containing tungsten compound and nickel compound for 2 hours at room temperature, and dried at 100°C for 6 hours to prepare a solution of ammonium dihydrogen phosphate with a weight concentration of 40%. The carrier was impregnated with the prepared phosphorus-containing solution for 2 hours, dried at 120°C for 5 hours, heat-treated at 400°C in an air atmosphere for 1 hour, and then activated with hydrogen in a hydrogen atmosphere. First, it was raised from room temperature at 10°C / min From 350°C to 600°C at a heating rate of 1°C / min to 350°C, and kept at 600°C for 4 hours to prepare transition metal phosphide catalyst C-2.
Embodiment 3
[0048] The carrier T-3 of Comparative Example 3 was impregnated with an impregnation solution containing tungsten and nickel at room temperature for 2 hours, and dried at 110°C for 6 hours to prepare a solution of ammonium hydrogen phosphate with a weight concentration of 60%. Immerse in a good phosphorus-containing solution for 2 hours, dry at 110°C for 5 hours, heat-treat at 350°C for 2 hours in an air atmosphere, and then perform an activation treatment in a hydrogen atmosphere, first rising from room temperature to 450°C at 8°C / min , at a heating rate of 1° C. / min, from 450° C. to 650° C., and kept at 650° C. for 4 hours to prepare transition metal phosphating catalyst C-3.
[0049] Table 1 Physicochemical properties of catalyst supports.
[0050] Numbering T-1 T-2 T-3 Molecular sieve, wt% 12.0 7.0 4.0 Amorphous silica-alumina, wt% 25.0 53.0 30.0 Macroporous alumina, wt% 43.0 20.0 46.0 Binder, wt% 20.0 20.0 20.0 Pore vol...
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