Hydroprocessing catalyst and its uses
A hydrogenation treatment and catalyst technology, applied in refining to remove heteroatoms, etc., can solve the problems of eased operating conditions, reduced stability, expensive precious metals, etc., and achieve less sulfur loss, improved stability, and good stability Effect
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Embodiment 1
[0033] A preparation method of the catalyst of the present invention
[0034] Take SB powder and Y zeolite (provided by Wenzhou Catalyst Factory, unit cell parameter is 2.464nm, silicon-aluminum molar ratio is 27, sodium oxide content is 0.08wt%, specific surface area is 692m 2 / g, the pore volume is 0.41ml / g) and zinc oxide powder are thoroughly mixed, impregnated with a solution containing ammonium fluoride, nickel nitrate and ammonium tungstate, dried at 120°C for 8 hours and activated at 500°C for 4 hours. The obtained catalyst powder is pressed into tablets, and crushed into 60-80 mesh particles to obtain a catalyst, numbered E-1. The composition and properties of the catalyst are shown in Table 3, and the results of the micro-reverse evaluation are shown in Table 4.
Embodiment 2
[0036] A preparation method of the catalyst of the present invention
[0037] Take amorphous silicon aluminum dry glue powder (SiO 2 The content is 18wt%), zinc carbonate, ZSM-5 (provided by Nankai University, the molar ratio of silicon to aluminum is 48), SB powder and methylcellulose are thoroughly mixed, and then an appropriate amount of 66wt% of nitric acid and an appropriate amount of water are added for extrusion molding. After drying at 100°C for 12 hours and calcining at 600°C for 3 hours, a catalyst carrier was obtained. Take an appropriate amount of the carrier, first saturated with a solution containing ferric nitrate, dried at 200°C for 6 hours, and then impregnated with a solution containing nickel carbonate, ammonium molybdate and phosphoric acid, dried at 80°C for 6 hours, and calcined at 550°C for 4 hours. A catalyst was obtained, numbered E-2. The composition and properties of the catalyst are shown in Table 3, the conditions and results of the micro-reverse evalu...
Embodiment 3
[0039] A preparation method of the catalyst of the present invention
[0040] Take amorphous titanium aluminum dry rubber powder (TiO 2 The content is 7wt%), zinc chloride powder, SB powder and Sesbania powder are thoroughly mixed, and then extruded with acetic acid, citric acid and an appropriate amount of water as a peptizer, dried at 200°C for 2 hours, and calcined at 550°C for 8 hours to obtain Catalyst carrier. Take an appropriate amount of the carrier, impregnate it with a solution containing cobalt carbonate, ammonium molybdate, phosphoric acid and ferric chloride, then dry at 120°C for 4 hours and calcinate at 480°C for 6 hours to obtain a catalyst, numbered E-3. The composition and properties of the catalyst are shown in Table 3, and the conditions and results of the micro-reverse evaluation are shown in Table 4.
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