A kind of preparation method of heavy oil hydrogenation demetallization catalyst
A heavy oil hydrogenation and catalyst technology, which is applied in the direction of catalyst activation/preparation, metal/metal oxide/metal hydroxide catalyst, chemical instruments and methods, etc., can solve the problem that the pore volume of the catalyst needs to be further improved, and achieve the benefit of transmission Mass and diffusion, high metal capacity, and the effect of extending the operating cycle
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[0037] Preparation of pretreatment material A:
[0038] Get the waste catalyst pulverized to more than 230 mesh, roast at 750 DEG C for 8 hours, weigh 100 grams of the above-mentioned waste catalyst, place 700 grams in an aqueous ammonium bicarbonate solution with a mass percentage concentration of 20%, and transfer the mixture into the autoclave After sealing, heat treatment was performed at 145°C for 6 hours, and then the powder was dried at 110°C for 6 hours. The above alumina was immersed and soaked for 1.5 hours with a solution of polyethylene glycol-6000 with a concentration of 30% by mass (ie, the average molecular weight was 6000), and then the carrier was dried at 120 ° C for 6 hours to obtain the pretreatment material A-I.
[0039] Take the waste catalyst pulverized to more than 230 meshes, roast at 800 ° C for 8 hours, weigh 100 grams of the above-mentioned waste catalyst, place 600 grams in an aqueous ammonium bicarbonate solution with a mass percentage concentrati...
Embodiment 1
[0044] Weigh 100 grams of pseudo-boehmite, 20 grams of the above-mentioned pretreatment materials A-I, 16 grams of the pretreatment materials B-I, and 2 grams of saffron powder, mix the above-mentioned physicals evenly, add an appropriate amount of an aqueous solution containing 3 grams of acetic acid, knead, and squeeze. The strip was formed, the formed product was dried at 140° C. for 6 hours, and the dried product was calcined at 700° C. in air for 5 hours to prepare an alumina carrier.
[0045] Weigh 50 grams of each of the above alumina carriers, add 100 mL of Mo-Ni-P solution (so that the final catalyst contains MoO 3 10.3wt%, containing NiO 3.1wt%) immersed for 2 hours, filtered off the excess solution, dried at 120°C, and calcined at 450°C for 5 hours to obtain the demetallization catalyst Cat-1 of the present invention. The properties of the catalyst are shown in Table 1. .
Embodiment 2
[0047] Same as Example 1, except that the addition amount of pretreatment material A-I is 25 grams, and the addition amount of pretreatment material B-I is 14 grams, the demetallation catalyst Cat-2 of the present invention is obtained, and the catalyst properties are shown in Table 1.
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