Hydrorefining catalyst and preparation method thereof
A technology for hydrorefining and catalyst, which is applied in chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, etc., and can solve the problems of low activity and short service life of catalysts
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[0037] The present invention also provides a kind of preparation method of hydrorefining catalyst, and this preparation method comprises the following steps:
[0038] (1) impregnating the γ-alumina carrier in a mixture containing urea, a water-soluble salt of metal component C and water, and obtaining a modified alumina carrier through heat treatment, filtration, washing and drying;
[0039] (2) introducing metal component A and metal component B to the modified alumina carrier obtained in step (1), wherein,
[0040] Metal component A is at least one of the metal elements selected from Group VIII, metal component B is at least one of the metal elements selected from Group VIB, and metal component C is at least one of the divalent metal elements One, and metal component C is different from both metal component A and metal component B.
[0041] According to the present invention, in the mixture, the concentration of the water-soluble salt of metal component C is preferably 0.05...
Embodiment 1
[0080] (1) 75.0g of γ-Al 2 o 3 The carrier was immersed in a solution of 250.0g deionized water, 9.0g urea, 4.0g ammonium nitrate and 14.6g cobalt nitrate hexahydrate, heat treated at 85°C for 18 hours, filtered, washed and then dried at 120°C for 3 hours to obtain Co modified The alumina support, the SEM image of the Co-modified alumina support is as follows figure 1 shown. From figure 1 It can be seen that the surface of the alumina carrier has a large number of network structures, and the network density is listed in Table 1.
[0081] (2) Prepare 48 mL of a solution containing 12.5 g of molybdenum trioxide and 4.1 g of phosphoric acid, impregnate the Co-modified alumina carrier obtained in step (1) for 1 hour, dry at 120° C. for 4 hours, and then Immerse in 40mL of an aqueous solution containing 27.3g of ammonium metatungstate for 1 hour, dry at 120°C for 4 hours, and bake at 450°C for 3 hours in an air flow of 100mL / min. After cooling down to room temperature, continue...
Embodiment 2
[0092] (1) 75.0g of γ-Al 2 o 3 The carrier was soaked in a solution of 250.0g deionized water, 13.5g urea, 2.4g ammonium chloride and 7.3g cobalt nitrate hexahydrate, heat treated at 70°C for 24 hours, filtered, washed and then dried at 150°C for 2 hours to obtain Co modified permanent alumina carrier;
[0093] (2) Immerse the Co-modified alumina carrier obtained in step (1) in 48 mL of aqueous solution containing 10.3 g of phosphoric acid for 1 hour, then dry at 120° C. for 4 hours, and roast at 450° C. for 3 hours in an air stream of 100 mL / min. After reaching room temperature, immerse in 45mL aqueous solution containing 15.3g ammonium paramolybdate, 27.3g ammonium metatungstate, 24.2g nickel nitrate hexahydrate and 42.6g citric acid for 1 hour, and dry at 150°C for 4 hours to obtain catalyst S-2 . Catalyst S-2 grid density and composition are listed in Table 1.
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