Preparation method of low-sodium copper zinc aluminum hydrogenation catalyst
A copper-zinc-aluminum catalyst, hydrogenation catalyst technology, applied in chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, etc.
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Embodiment 1
[0014] According to the formula and process of the CO hydrogenation catalyst, the ternary matrix of the copper-zinc-aluminum hydrogenation catalyst obtained by using sodium bicarbonate as the precipitant of the matrix is filtered and dried, and then granulated. After 100 minutes, the loss on ignition of the particles was measured, and then the particles after the initial calcination were washed five times with 80°C deionized water, and the sodium content of the catalyst body was tested, and the sodium content was less than or equal to 200ppm (measured as Na 2 O meter), after qualified, the washed and filtered particles were baked at 100°C for 12 hours, and after drying, the particles were calcined for a second time at 350°C for 30 minutes to form the catalyst Cat1-a.
Embodiment 2
[0018] According to the formula and process of mixed butyraldehyde hydrogenation catalyst, the ternary matrix of copper-zinc-aluminum hydrogenation catalyst obtained by using the mixed solution of sodium carbonate and sodium bicarbonate as the precipitant of the matrix is filtered and dried, and then granulated. Carry out the initial calcination, the calcination time is 60min, measure the loss on ignition of the particles, then wash the particles six times with 70°C deionized water, test the sodium content of the catalyst body, wash and filter the particles after passing the test, bake at 120°C for 10h, dry them in The particles were calcined for a second time at 340° C. for 45 minutes, and the catalyst Cat2-a was obtained by molding.
Embodiment 3
[0022] According to the formula and process of octenal hydrogenation reaction catalyst, the ternary matrix of copper-zinc-aluminum hydrogenation catalyst obtained by using sodium hydroxide as the precipitant of the matrix is filtered and dried, and then granulated. The calcination time is 20 minutes, and the loss on ignition of the particles is measured, and then the particles after the initial calcination are washed five times with 60°C deionized water, and the sodium content of the catalyst body is tested. After passing the washing, the filtered particles are baked at 90°C for 12 hours, and dried at 300°C The particles were calcined for 60 minutes twice to form the catalyst Cat3-a.
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