Preparation method for metal phosphide type hydrocracking catalyst
A metal phosphide and hydrocracking technology, which is applied in physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problems of unstable properties of heteropolyacids and insufficient stability of catalysts, etc.
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Embodiment 1
[0036] 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 then place it under a hydrogen atmosphere. Reduction activation, the reduction activation procedure is to rise from room temperature to 450°C at 5°C / min, from 450°C to 700°C at a heating rate of 2°C / min, and keep the temperature at 700°C for 2 hours to prepare the catalyst of the present invention C-1.
[0037] Through XRD analysis (under nitrogen protection condition), it can be seen that there are tungsten phosphide (WP) and nickel phosphide (Ni phosphide) in the catalyst of the present invention. 2 The characteristic diffraction peak of P) forms the phosphating state of the active metal.
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 then in a hydrogen atmosphere Activation of hydrogen at 10°C / min from room temperature to 350°C at 1°C / min, from 350°C to 600°C at a rate of 1°C / min, and at 600°C for 4 hours to prepare transition metal phosphides Catalyst C-2.
Embodiment 3
[0047] Prepare an impregnating solution with a weight concentration of 40% ammonium hydrogen phosphate and containing 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 then place it in a hydrogen atmosphere. For activation treatment, first raise from room temperature to 450°C at 8°C / min, then rise from 450°C to 650°C at a heating rate of 1°C / min, and keep the temperature at 650°C for 4 hours to prepare a 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
[0050] Table 2 Catalyst composition and pr...
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