Preparation method for hydrogenation catalyst
A hydrogenation catalyst, catalyst technology, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc. , poor strength of interaction catalyst, etc.
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[0024] The preparation method of hydrogenation catalyst provided by the invention, a kind of specific process is as follows:
[0025] 1. Ni x W y o z Precursor mixtures of composite oxides and alumina with MoO 3 Preparation of the mixture
[0026] Prepare a salt mixed solution A containing active metal Ni, W component, aluminum and additives. The nickel-containing salt can be one or more of nickel sulfate, nickel nitrate, nickel chloride, etc. The tungsten-containing salt can be one or more of sodium tungstate, ammonium metatungstate and the like. The aluminum-containing salt may be one or more of aluminum chloride, aluminum nitrate, aluminum sulfate, and the like. Auxiliaries generally include one or more of P, F, Ti, Si, B, Zr, etc. Alkaline solution B containing aluminum is prepared, and the alkaline solution containing aluminum is preferably sodium metaaluminate solution. Add material A and material B concurrently into the reaction tank with clean water to form a ge...
Embodiment 1
[0035]Add 500mL of water into the dissolution tank 1, dissolve 40g of nickel chloride, then add 44g of ammonium metatungstate to dissolve, then add 26g of aluminum nitrate to dissolve, and prepare acidic working solution A. Add 500mL of water into the dissolution tank 2, then add 20g of sodium metaaluminate to dissolve, and prepare alkaline working solution B. Add 350mL of water into the reaction tank, and the temperature rises to 60°C. Under the condition of stirring, add solution A and solution B into the reaction tank concurrently to form gel, the gel forming temperature is 60°C, the gel forming time is 0.5 hour, and the pH value of the slurry during the gel forming process is 7.5. Aging for 1 hour after gel forming. Then filter, add 600ml of clean water and 18g of molybdenum trioxide to the filter cake, beat and stir evenly, filter, dry the filter cake at 80°C for 5 hours, then extrude into strips, wash with clean water for 3 times, and dry the wet strips at 120°C for 5 h...
Embodiment 2
[0037] According to the method of Example 1, according to the component content ratio of catalyst B in Table 1, nickel chloride, ammonium metatungstate, aluminum nitrate and zirconium oxychloride were added to the dissolution tank 1 to prepare acidic working solution A. Add sodium metaaluminate to dissolving tank 2 to prepare alkaline working solution B. Add 350mL of water into the reaction tank, and the temperature rises to 40°C. Under the condition of stirring, add solution A and solution B into the reaction tank concurrently to form gel, the gel forming temperature is 40°C, the gel forming time is 2 hours, and the pH value of the slurry during the gel forming process is 8.0. Aging for 2 hours after gel forming. Then filter, wash the filter cake twice with 500mL of clean water, add clean water and molybdenum trioxide, beat and stir evenly, filter, dry the filter cake at 70°C for 7 hours, then extrude it, wash it twice with clean water, wet the bar It was dried at 100°C for...
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