Desulfurization catalyst, preparation method thereof and hydrocarbon oil desulfurizing method
A technology for desulfurization catalysts and oxides, which is applied in the direction of refined hydrocarbon oil, molecular sieve catalysts, chemical instruments and methods, and can solve the problems of reduced activity of adsorbents, etc.
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[0043] The present invention also provides a method for preparing a desulfurization catalyst, the method comprising: (1) subjecting a mixed solution obtained by mixing a lead-containing compound, a zinc-containing compound and water to a precipitation reaction, and filtering, drying, and roasting to obtain a precipitated product; (2) contacting a silicon oxide source, a non-aluminum oxide precursor, a molecular sieve with a BEA structure and / or a molecular sieve with a FAU structure, water and an acid solution to form a slurry, and the step (1) obtains The precipitated product is mixed with the slurry to form a carrier mixture; then the carrier mixture is shaped, dried and calcined to form a carrier; (3) a compound containing an active metal is introduced into the carrier obtained in step (2) and dried and calcined to obtain a desulfurization catalyst precursor; the active metal is at least one of cobalt, nickel, iron and manganese; (4) reducing the desulfurization catalyst pre...
Embodiment 1
[0084] This example is used to illustrate the preparation method of the desulfurization catalyst of the present invention.
[0085] (1) Preparation of the precipitated product. Mix 10.9 kg of zinc acetate dihydrate powder (produced by Beijing Chemical Factory, analytical grade), 0.86 kg of lead acetate trihydrate (Sinopharm Chemical Reagent Co., Ltd., analytical grade) and 18 kg of deionized water, stir for 30 minutes and dissolve completely. The precipitated product obtained by adding 1.8 kg of ammonia water was filtered and dried at 150° C. for 2 hours, and then calcined at 500° C. for 1 hour to obtain the precipitated product C1.
[0086] The precipitated product C1 was subjected to fluorescence analysis and XRD measurement. XRD spectrum (see figure 1 ) has no diffraction peaks of PbO, and the standard diffraction peaks of ZnO appear to shift 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
[0095] This example is used to illustrate the preparation method of the desulfurization catalyst of the present invention.
[0096] (1) Preparation of the precipitated product. Mix 14.0 kg of zinc nitrate hexahydrate (produced by Beijing Chemical Factory, analytically pure), 1.80 kg of lead nitrate powder (Sinopharm Chemical Reagent Co., Ltd., analytically pure) and 18 kg of deionized water, stir for 30 minutes, add 2.0 kg of urea and heat to A white precipitate was obtained after treatment at 80°C for 2 hours. After filtration, it was first dried at 150°C for 2 hours, and then calcined at 500°C for 1 hour to obtain a precipitated product C2.
[0097] The precipitated product C2 was subjected to fluorescence analysis and XRD measurement. XRD spectrum (see figure 1 ) has no diffraction peaks of PbO, and the standard diffraction peaks of ZnO appear to shift to the right, where A 100 -B 100 =0.25°, A 002 -B 002 =0.24°, A 101 -B 101 =0.24°, indicating that PbO and ZnO in t...
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