Method for preparing benzhydrol by hydrogenation of benzophenone
A technology of benzophenone and benzphenyl alcohol, which is applied in the field of hydrogenation of benzophenone to produce benzphenyl alcohol, can solve the problems of unfavorable large-scale industrial production separation, difficult industrial application, expensive catalyst, etc., and achieve easy large-scale industrialization Effects on production, sintering inhibition, excellent conversion and selectivity
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Embodiment 1
[0029] Mix 4.3 g of copper nitrate, concentrated ammonia water, and deionized water at room temperature to prepare a mixture with a pH of 9.5 to 12.5, add 5.75 g of powdered aluminum oxide to it, and stir for 12 hours at room temperature. The temperature rises to 120°C, and the pH value of the mixed solution is monitored in real time until it drops to 6-7. Filter and wash with deionized water. The obtained solid sample was dried in an oven at 100°C for 6 hours, and then transferred to a muffle furnace for calcination at 650°C for 3 hours to obtain a catalyst Cu / Al 2 O 3 .
[0030] Take 0.1g of the above catalyst and place it in a connected high-temperature reduction furnace to reduce the catalyst. The reduction temperature is 350℃, the reduction time is 1h, the reduction pressure is 0.3MPa, the reducing gas is hydrogen, and the gas space velocity is 3000h. -1 . After the reduction, the temperature was lowered to room temperature and switched to nitrogen. Under the protection of ...
Embodiment 2
[0032] Mix 4.3 g of copper nitrate, concentrated ammonia water, and deionized water at room temperature to prepare a mixture with a pH of 9.5 to 12.5, add 5.75 powdered aluminum oxide to it, and stir for 12 hours at room temperature. The temperature rises to 120°C, and the pH value of the mixed solution is monitored in real time until it drops to 6-7. Filter and wash with deionized water. The obtained solid sample was dried in an oven at 100°C for 6 hours, and then transferred to a muffle furnace for calcination at 650°C for 3 hours to obtain a catalyst Cu / Al 2 O 3 .
[0033] Weigh the 2.0 g sample prepared above, immerse it in an equal volume of the aqueous solution containing palladium nitrate for 36 hours, and dry it in an oven at 100°C for 6 hours. Then transfer to a muffle furnace for calcination at 650°C for 6 hours. The component in the obtained catalyst is Cu-Pd / Al 2 O 3 .
[0034] Take 0.1g of the above catalyst and place it in a connected high-temperature reduction fur...
Embodiment 3
[0036] Mix 4.3 g of copper nitrate, concentrated ammonia water, and deionized water at room temperature to prepare a mixture with a pH of 9.5 to 12.5, add 5.75 g of powdered aluminum oxide to it, and stir for 12 hours at room temperature. The temperature rises to 120°C, and the pH value of the mixed solution is monitored in real time until it drops to 6-7. Filter and wash with deionized water. The obtained solid sample was dried in an oven at 100°C for 6 hours, and then transferred to a muffle furnace for calcination at 650°C for 3 hours to obtain a catalyst Cu / Al 2 O 3 .
[0037] Weigh the 2.0 g sample prepared above, immerse it in an equal volume of an aqueous solution containing magnesium nitrate for 36 hours, and dry it in an oven at 100°C for 6 hours. Then transfer to a muffle furnace for calcination at 650°C for 6 hours. The component in the obtained catalyst is Cu-Mg / Al 2 O 3 .
[0038] Take 0.1g of the above catalyst and place it in a connected high-temperature reduction...
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