Preparation method of metal phosphide type hydrocracking catalyst
A metal phosphide, hydrocracking technology, 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 catalyst stability.
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Embodiment 1
[0037] Using the impregnating solution of Comparative Example 1, add red phosphorus at a ratio of W to P molar ratio of 1:1 and Ni to P molar ratio of 2:1, and use an ultrasonic wave with a frequency of 18KHz and a power of 100W / L to disperse for 1 hour. Carrier T-1 was impregnated at room temperature for 2 hours. While impregnated, it was dispersed by ultrasonic waves with a frequency of 18KHz and a power of 100W / L, then dried at 120°C for 4 hours, and then reduced and activated in a hydrogen atmosphere. The reduction activation procedure is to raise 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 C-1 of the present invention .
[0038] 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...
Embodiment 2
[0043] Using the impregnating solution of Comparative Example 1, add red phosphorus at the ratio of W to P molar ratio of 1:1.5 and Ni to P molar ratio of 1:1, and use ultrasonic wave with frequency of 25KHz and power of 150W / L to disperse for 5 hours. Carrier T-2 was impregnated at room temperature for 4 hours. While impregnating, it was dispersed by ultrasonic waves with a frequency of 25KHz and a power of 150W / L. Dry at ℃ for 6 hours, and then perform hydrogen activation under a hydrogen atmosphere. Firstly, increase from room temperature to 350℃ at a rate of 10℃ / min, then increase from 350℃ to 600℃ at a rate of 1℃ / min, and keep the temperature at 600℃ After 4 hours, the phosphating transition metal catalyst C-2 was prepared.
Embodiment 3
[0048] With the impregnating solution of Comparative Example 1, red phosphorus was added at the ratio of W to P molar ratio of 1:2 and Ni to P molar ratio of 1:1, and ultrasonic dispersion with a frequency of 35KHz and a power of 10W / L was used for 7 hours. Carrier T-3 was impregnated at room temperature for 4 hours, while impregnating with ultrasonic dispersion with a frequency of 35KHz and a power of 10W / L, dried at 110°C for 6 hours, and then activated in a hydrogen atmosphere. Raise from room temperature to 450°C at 8°C / min, from 450°C to 650°C at a rate of 1°C / min, and keep the temperature at 650°C for 4 hours to prepare transition metal phosphide 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 volume, ml / g 0...
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