Catalyst for preparing 3-pentanol through 3-pentanone hydrogenation and preparation method of catalyst for preparing 3-pentanol through 3-pentanone hydrogenation
A catalyst, pentanone technology, applied in chemical instruments and methods, hydroxyl compound preparation, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problems of long reaction time, non-compliance with green chemical industry, environmental pollution, etc. The preparation and production methods are simple and easy to implement, the burden of product separation is reduced, and the production cost is reduced.
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Embodiment 1
[0024] Weigh 0.008g of cerium nitrate hexahydrate, put it into 50ml of deionized water, add 0.6g of activated carbon, adjust pH=10 with ammonia water after stirring for 3h, keep stirring for 3h, filter and wash. Dry in vacuum at 60°C for 12h. In nitrogen, the temperature was raised to 400°C at 5°C / min, and the temperature was kept constant for 3h to cool down to room temperature. Ce / C is produced.
[0025] Weigh 0.024g of ruthenium chloride hydrate and 0.024g of copper chloride hydrate into 50ml of ethylene glycol, and stir for 30min. Put the Ce / C prepared in the previous step into the above solution, adjust the pH to 10 with sodium hydroxide, stir and raise the temperature to 230° C. for 2 hours. Cool down to room temperature, filter and wash, and dry under vacuum at 60°C for 12h. In nitrogen, the temperature was raised to 400°C at 6°C / min, and the temperature was kept at room temperature for 2 hours to prepare a Ru-Cu-Ce / C catalyst, in which the loading amount of Ru was 0...
Embodiment 2
[0027] Weigh 0.008g of lanthanum nitrate hexahydrate, put it into 50ml of deionized water, add 0.6g of carbon black, stir for 3h, adjust pH=12 with sodium hydroxide, keep stirring for 2h, filter and wash. Vacuum dry at 40°C for 14h. In nitrogen, the temperature was raised to 500°C at 5°C / min, and the temperature was kept constant for 3h to cool down to room temperature. La / C was prepared.
[0028] Weigh 0.015g of ruthenium chloride hydrate and 0.015g of chloroauric acid, put them into 50ml of deionized water, and stir for 30min. Put the La / C prepared in the previous step into the above solution, adjust the pH to 3 with hydrochloric acid, and stir at room temperature for 12 h. Infrared lamp rapid drying, vacuum drying at 60 ℃ for 10h. In hydrogen, the temperature was raised to 230°C at 3°C / min, and then the temperature was lowered to room temperature after 8h to prepare the Ru-Au-La / C catalyst, in which the loading amount of Ru was 0.1%-1.7%, and the loading amount of Au was...
Embodiment 3
[0030]Weigh 0.008g of yttrium nitrate hexahydrate, put it into 50ml of deionized water, add 0.6g of carbon nanotubes, stir for 3 hours, adjust the pH to 12 with sodium hydroxide, keep stirring for 5 hours, filter and wash, and vacuum dry at 80°C for 12 hours . In nitrogen, the temperature was raised to 500°C at 5°C / min, and the temperature was kept constant for 3h to cool down to room temperature. Y / C was prepared.
[0031] Weigh 0.01g of chloroiridic acid hydrate and 0.01g of silver nitrate, put them into 50ml of deionized water, and stir for 30min. Put the Y / C prepared in the previous step into the above solution, adjust the pH to 2 with 10% hydrochloric acid, and stir at room temperature for 8 hours. Infrared lamp rapid drying, 60 ℃ vacuum drying for 12h. In hydrogen, the temperature was raised to 200°C at 2°C / min, and the temperature was kept at room temperature for 6 hours to prepare the Ag-Ir-Y / C catalyst, in which the loading of Ag was 0.1%-1.7%, and the loading of I...
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