Desulfurization catalyst, preparation method thereof and hydrocarbon oil desulfurizing method
A desulfurization catalyst, alumina technology, which is applied in the fields of refined hydrocarbon oil, molecular sieve catalyst, chemical instruments and methods, etc., can solve the problem of reducing the activity of adsorbents
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[0048] The present invention also provides a method for preparing a desulfurization catalyst. The method includes: (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 filtering the mixture obtained by the precipitation reaction. Roasting to obtain a precipitated product; (2) contacting layered pillared clay, alumina source, molecular sieve with BEA structure and / or molecular sieve with FAU structure, water and acid solution to form a slurry, and combining the precipitated product obtained in step (1) 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 desulfurization Catalyst precursor; the active metal is at least one of cobalt, nickel, iron and manganese; (4) reduc...
Embodiment 1
[0088] This example is used to illustrate the preparation method of the desulfurization catalyst of the present invention.
[0089] (1) Prepare precipitation product. Mix 10.9 kilograms of zinc acetate dihydrate powder (produced by Beijing Chemical Plant, analytically pure), 0.86 kilograms of lead acetate trihydrate (Sinopharm Chemical Reagent Company, analytically pure), and 18 kilograms of deionized water. Stir for 30 minutes and then completely dissolve. 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.
[0090] The precipitated product C1 was subjected to fluorescence analysis and XRD measurement. XRD spectrum (see figure 1 ) There is 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 precipitation pr...
Embodiment 2
[0098] This example is used to illustrate the preparation method of the desulfurization catalyst of the present invention.
[0099] (1) Prepare precipitation 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 A white precipitate was obtained after treatment at 80°C for 2 hours. After filtration, it was dried at 150°C for 2 hours, and then calcined at 500°C for 1 hour to obtain precipitated product C2.
[0100] The precipitation product C2 was subjected to fluorescence analysis and XRD measurement. XRD spectrum (see figure 1 ) There is 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 precipitation product C2 all form a ...
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