Catalyst for preparing 3-pentanol by hydrogenation of 3-pentanone and preparation method thereof
A catalyst, pentanone technology, applied in chemical instruments and methods, preparation of hydroxyl compounds, metal/metal oxide/metal hydroxide catalysts, etc., can solve the problems of long reaction time, non-compliance with green chemical industry, environmental pollution, etc. To achieve the effect of simple and easy preparation and production methods, reducing the burden of product separation, and reducing production costs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
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...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com