A kind of preparation method of highly active residual oil hydrodemetallization catalyst
A technology for hydrogenation and demetallization of residue oil, which is applied in catalyst activation/preparation, metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, etc. The effect of improving sulfidation, desulfurization activity, and demetallization activity
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example 1
[0023] Weigh 100 grams (25% water content) of the above-mentioned self-made clover-shaped alumina and transfer it into the polytetrafluoroethylene lining of the autoclave, add 150 ml of the aqueous solution dissolved in 228 grams of xylitol, and make the alcohol and Al 3+ The molar ratio was 1:1, immersion for 60 minutes, the autoclave was sealed and transferred to an oven, sealed at 150°C, heat-treated under autogenous pressure for 9 hours, and cooled to room temperature naturally. The alumina carrier after hydrothermal treatment was dried at 120°C for 3 hours. With 150ml containing MoO 3 105 g, 15 g of NiO impregnating solution impregnated the above-mentioned carrier for 3 hours, filtered off excess solution, dried at 110 ° C for 8 hours, the dried material was first roasted at 550 ° C under nitrogen atmosphere for 5 hours, and then in an air atmosphere at Bake at 350°C for 2 hours. The residue hydrodemetallization catalyst C1 of the present invention is prepared.
example 2
[0025] The same as Example 1, except that the alumina carrier was impregnated with 150 ml of an aqueous solution containing 136.5 grams of sorbitol, so that the alcohol and Al were impregnated. 3+ The molar ratio is 0.5:1, the immersion is 80 minutes, the temperature during heat treatment is 200° C., and the treatment time is 6 hours, so as to prepare the residue hydrodemetallation catalyst C2 of the present invention.
example 3
[0027] The same as Example 1, except that the alumina carrier was impregnated with 150 ml of an aqueous solution containing 81.9 g of mannitol, so that the alcohol and Al were impregnated. 3+ The molar ratio is 0.3:1, the immersion is 90 minutes, the temperature during heat treatment is 175° C., and the treatment time is 12 hours, so as to prepare the residue hydrodemetallation catalyst C3 of the present invention.
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