Desulfurization catalyst, preparation method thereof and hydrocarbon oil desulfurizing method
A desulfurization catalyst, alumina technology, applied in the direction of refined hydrocarbon oil, molecular sieve catalyst, chemical instruments and methods, etc., can solve the problem of reduced activity of adsorbents
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[0044] 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 silica source, an alumina source, an alkali metal compound, 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) The obtained precipitation 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, Roasting to obtain a desulfurization catalyst precursor; the active metal is at least one of cobalt, nickel, iron and manganese; (4) reducing the desulfurization catalyst...
Embodiment 1
[0087] This example is used to illustrate the preparation method of the desulfurization catalyst of the present invention.
[0088] (1) Prepare the precipitated product. 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.
[0089] 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 precipitated ...
Embodiment 2
[0097] This example is used to illustrate the preparation method of the desulfurization catalyst of the present invention.
[0098] (1) Prepare the precipitated product. Mix 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, stir for 30 minutes, add 2.0 kg of urea and heat 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.
[0099] 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 that PbO and ZnO in the precipi...
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