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 insufficient catalyst stability and unstable properties of heteropolyacids
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Embodiment 1
[0037] Prepare an impregnation solution with a weight concentration of 30% ammonium dihydrogen phosphate, tungsten and nickel, impregnate the carrier T-1 of Comparative Example 1 with the prepared impregnation solution for 2 hours, dry at 120°C for 4 hours, and dry at 120°C for 4 hours. Heat treatment at ℃ for 6 hours, and then reductive activation under hydrogen atmosphere. The reductive activation program is to rise from room temperature to 450°C at a rate of 5°C / min, and to rise from 450°C to 700°C at a heating rate of 2°C / min. The catalyst C-1 of the present invention was prepared by keeping the temperature at 700°C for 2 hours.
Embodiment 2
[0042] Prepare an impregnating solution with a weight concentration of 40% ammonium dihydrogen phosphate and containing tungsten and nickel, impregnate the carrier T-2 of Comparative Example 2 with the prepared impregnating solution for 2 hours, dry at 100°C for 6 hours, and place in an air atmosphere Heat treatment at 400°C for 1 hour, and then perform hydrogen activation under a hydrogen atmosphere. Firstly, heat up from room temperature to 350°C at a rate of 10°C / min, then rise from 350°C to 600°C at a rate of 1°C / min. The temperature was kept at 600° C. for 4 hours to prepare the phosphating transition metal catalyst C-2.
Embodiment 3
[0047] Prepare an impregnating solution with a weight concentration of 40% ammonium hydrogen phosphate and tungsten and nickel, impregnate the carrier T-3 of Comparative Example 3 with the prepared impregnating solution for 2 hours, dry at 110°C for 6 hours, and dry at 350 °C in an air atmosphere. Heat treatment at ℃ for 2 hours, and then under hydrogen atmosphere, conduct activation treatment, firstly increase from room temperature to 450 ℃ at 8 ℃ / min, increase from 450 ℃ to 650 ℃ at a heating rate of 1 ℃ / min, and at 650 °C for 4 hours to prepare the phosphating transition metal catalyst C-3.
[0048] Table 1 Physicochemical properties of catalyst supports.
[0049] 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 volume, ml / g 0.73 0.76 0.78 Specific surface area, m 2 / g 425 392 383
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