Method for catalyzing gasoline deep desulfurization with Ni-Mo-Co containing catalyst
A ni-mo-co, deep desulfurization technology, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc. Technical requirements, unseen problems, etc., to achieve the effect of reducing the severity of the reaction, optimizing the loss of octane number, and optimizing the hydrogen consumption
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[0031] Example 1:
[0032] Weigh 100g pseudo-boehmite, add 2.5g sesame powder, and then add 3% nitric acid aqueous solution, knead and extrude, dry at 120°C for 4h, and then calcinate at 650°C for 4h to prepare a catalyst carrier. Test the water absorption of the carrier according to the conventional method, and then configure the active component dipping solution according to the water absorption of the carrier according to the equal volume dipping method. First, weigh out 45ml of ammonia, then add 2g of ammonium molybdate, 3g of cobalt nitrate, and 51g of nickel nitrate in sequence and stir to dissolve, and finally make the volume constant with ammonia. The carrier was impregnated with an equal volume impregnation method to make the catalyst carrier fully absorb the active component impregnation solution, and then placed for 12 hours, the catalyst was dried at 120°C for 4 hours, and calcined at 500°C for 4 hours to prepare a catalyst sample Cat-1#.
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[0033] Example 2:
[0034] According to the carrier preparation method in Example 1, 100 g of the catalyst carrier was prepared, and then the active component impregnation solution was configured. The preparation method was the same as in Example 1. First, weigh 50ml of ammonia, then add 4g of ammonium molybdate, 10g of cobalt nitrate, and 62g of nickel acetate in sequence and stir to dissolve, and finally make the volume constant with ammonia. The metal active component impregnation method, drying and calcination conditions were the same as in Example 1, and the catalyst sample Cat-2# was prepared.
Example Embodiment
[0035] Example 3:
[0036] According to the carrier preparation method in Example 1, 100 g of the catalyst carrier was prepared, and then the active component impregnation solution was prepared, and the catalyst was prepared by impregnation in two steps. First, weigh 40ml of ammonia, then add 4g of ammonium molybdate, 6g of cobalt nitrate, and 34g of nickel acetate and stir until it dissolves, and finally make the volume constant with ammonia. The metal active component impregnation method, drying and roasting conditions were the same as in Example 1. A primary impregnated catalyst sample was prepared; the above catalyst sample was impregnated twice, 40ml ammonia water was weighed, and then 4g ammonium molybdate, 6g cobalt nitrate and 21g acetic acid were added. The nickel is stirred until it dissolves, and finally the volume is made constant with ammonia water. The metal active component impregnation method, drying and calcination conditions were the same as in Example 1, and t...
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