Method for preparing hydrogenation catalyst composite
A hydrogenation catalyst and composition technology, applied in chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, etc., can solve the problem of high catalyst metal content, loss of activity, no discovery Active metal coordination effect and other problems, to achieve the effect of simple and reliable preparation process and overcoming difficult preparation
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[0019] The catalyst preparation method provided by the present invention, a kind of concrete process step is as follows:
[0020] 1. Ni x W y o z Complex oxide precursors and MoO 3 Preparation of the mixture
[0021] Prepare the salt mixed solution A containing the active metal Ni component and additives according to the content ratio of the catalyst components. The nickel-containing salt can be nickel sulfate, nickel nitrate, nickel chloride, etc. Auxiliaries generally include one or more of P, F, Ti, Si, B, Zr, etc., and aluminum salts, such as aluminum chloride, aluminum nitrate, and aluminum sulfate, can also be added as needed. The solution B containing the active metal W component is prepared according to the content ratio of the catalyst components. The W component in the solution B exists in the form of sodium tungstate, and the solution B is an alkaline solution. Add material A and material B concurrently into a reaction tank with clean water to form a gel. The g...
Embodiment 1
[0030] Add 500mL of water into the dissolution tank 1, and dissolve 42g of nickel chloride to prepare an acidic working solution A. Add 500mL of water into the dissolution tank 2, add 35g of sodium tungstate to dissolve, adjust the pH value with 77g of sodium metaaluminate, 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 in parallel 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 8.0. Aging for 1 hour after gel forming. Then filter, add 600ml of clean water and 12g of molybdenum trioxide to the filter cake, beat and stir evenly, filter, dry the filter cake at 80°C for 5 hours, then extrude it, wash it with clean water for 3 times, and dry the wet bar at 120°C for 5 hours , and calcined at 500°C for 4 hours to obtain the f...
Embodiment 2
[0032] According to the method of Example 1, according to the composition ratio of the catalyst B in Table 1, nickel chloride, zirconium oxychloride and aluminum chloride were added into the dissolution tank 1 to prepare an acidic working solution A. Add sodium tungstate to the dissolution tank 2 and adjust the pH value with sodium hydroxide 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 in parallel to form a 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 8.5. 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 ba...
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