A kind of desulfurization catalyst and its preparation method and the method for hydrocarbon oil desulfurization
A desulfurization catalyst and oxide technology, which is applied in the fields of refining hydrocarbon oil, molecular sieve catalysts, chemical instruments and methods, etc., can solve the problems of reducing the activity of adsorbents, etc.
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[0040] The present invention also provides a method for preparing a desulfurization catalyst, the method comprising: (1) performing a precipitation reaction on a mixed solution obtained by mixing a lead-containing compound, a zinc-containing compound and water, and filtering, drying and Roasting to obtain a precipitated product; (2) contacting a silicon oxide source, a non-aluminum oxide precursor, an aluminum phosphorus molecular sieve, water and an acid solution to form a slurry, and mixing the precipitated product obtained in step (1) with the slurry to form carrier mixture; then molding, drying and roasting the carrier mixture to form a carrier; (3) introducing a compound containing an active metal to the carrier obtained in step (2) and drying and roasting to obtain a desulfurization catalyst precursor; the active The metal is at least one of cobalt, nickel, iron and manganese; (4) reducing the desulfurization catalyst precursor obtained in step (3) under a hydrogen-contai...
Embodiment 1
[0081] This example is used to illustrate the preparation method of the desulfurization catalyst of the present invention.
[0082] (1) Precipitation product is prepared. Mix 10.9 kg of zinc acetate dihydrate powder (produced by Beijing Chemical Plant, analytically pure), 0.86 kg of lead acetate trihydrate (Sinopharm Chemical Reagent Company, analytically pure) and 18 kg of deionized water, and dissolve completely after stirring for 30 minutes. The precipitated product obtained by adding 1.8 kg of ammonia water was filtered, dried at 150° C. for 2 hours, and then calcined at 500° C. for 1 hour to obtain the precipitated product C1.
[0083] The precipitated product C1 was subjected to fluorescence analysis and XRD determination. In the XRD spectrum (see figure 1 ) has no diffraction peak of PbO, and the standard diffraction peak of ZnO shifts to the right, where A 100 -B 100 = 0.2°, A 002 -B 002 = 0.21°, A 101 -B 101 = 0.2°, indicating that PbO and ZnO in the precipita...
Embodiment 2
[0092] This example is used to illustrate the preparation method of the desulfurization catalyst of the present invention.
[0093] (1) Precipitation product is prepared. 14.0 kg of zinc nitrate hexahydrate (produced by Beijing Chemical Plant, analytically pure), 1.80 kg of lead nitrate powder (Sinopharm Chemical Reagent Company, analytically pure) and 18 kg of deionized water were mixed, and after stirring for 30 minutes, 2.0 kg of urea was added and heated to After treatment at 80°C for 2 hours, a white precipitate was obtained. After filtration, it was first dried at 150°C for 2 hours, and then calcined at 500°C for 1 hour to obtain the precipitated product C2.
[0094] The precipitated product C2 was subjected to fluorescence analysis and XRD determination. In the XRD spectrum (see figure 1 ) has no diffraction peak of PbO, and the standard diffraction peak of ZnO shifts to the right, where A 100 -B 100 = 0.25°, A 002 -B 002 = 0.24°, A 101 -B 101 =0.24°, indicating...
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