Preparation method of catalytic material mixed by copper and cerium oxide
A catalytic material, cerium oxide technology, applied in chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, etc., to achieve the effects of simple operation, high pore volume, and easy industrial production
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] (a) Take 0.06318g copper nitrate (Cu(NO 3 ) 2 ·3H 2 O) Dissolve in deionized water and stir continuously for 0.5h; the concentration of Cu ions is 0.00872mol / mL;
[0033] (b) According to the liquid-solid ratio of 8:1, add the mesoporous ceria powder into the copper salt solution obtained in step (a), after dissolving, let stand for 24 hours, and stir occasionally during the period;
[0034] (c) Put the mixed solution of step (b) in a constant temperature drying oven to dry at 110°C for 10 hours, then grind it and place it in a muffle furnace for sintering at 300°C for 2 hours to obtain a copper-doped cerium oxide catalytic material, which The specific surface area is 154.289m 2 / g, the pore volume is 0.975cm 3 / g.
[0035] Wherein, the mesoporous ceria powder is prepared through the following steps:
[0036] (1) Take 52.240g cerium nitrate (Ce(NO 3 ) 3 ·6H 2 O) and 5.2510 g of citric acid were dissolved in deionized water, and continuously stirred for 0.5 h to...
Embodiment 2
[0043] (a) Take 0.1972g copper nitrate (Cu(NO 3) 2 ·3H 2 O) Dissolve in deionized water and stir continuously for 0.8h; the concentration of Cu ions is 0.02616mol / mL;
[0044] (b) According to the liquid-solid ratio of 10:1, add the mesoporous ceria powder into the copper salt solution obtained in step (a), after dissolving, let stand for 36 hours, and stir occasionally during the period;
[0045] (c) Put the mixed solution of step (b) in a constant temperature drying oven to dry at 120°C for 12h, and then put it in a muffle furnace and bake at 280°C for 3h after grinding to obtain a copper-doped cerium oxide catalytic material, which The specific surface area is 150.976m 2 / g, the pore volume is 0.879cm 3 / g.
[0046] Wherein, the mesoporous ceria powder is prepared through the following steps:
[0047] (1) Take 17.3652g cerium nitrate (Ce(NO 3 ) 3 ·6H 2 O) and 1.72812g of citric acid were dissolved in deionized water and stirred continuously for 0.5h to obtain a cit...
Embodiment 3
[0054] (a) Take 0.3235g copper nitrate (Cu(NO 3 ) 2 ·3H 2 O) Dissolve in deionized water and stir continuously for 1h; the concentration of Cu ions is 0.0436mol / mL;
[0055] (b) According to the liquid-solid ratio of 6:1, add the mesoporous ceria powder into the copper salt solution obtained in step (a), after dissolving, let stand for 48 hours, and stir occasionally during the period;
[0056] (c) Put the mixed solution in step (b) in a constant temperature drying oven to dry at 120°C for 10 hours, and then grind it and place it in a muffle furnace and bake it at 200°C for 2.5 hours to obtain a copper-doped cerium oxide catalytic material. Its specific surface area is 147.630m 2 / g, the pore volume is 0.859cm 3 / g.
[0057] Wherein, the mesoporous ceria powder is prepared through the following steps:
[0058] (1) Take 30.8873g cerium nitrate (Ce(NO 3 ) 3 ·6H 2 O) and 3.1002g of citric acid were dissolved in deionized water, and continuously stirred for 0.8h to obtain...
PUM
Property | Measurement | Unit |
---|---|---|
specific surface area | aaaaa | aaaaa |
specific surface area | aaaaa | aaaaa |
specific surface area | aaaaa | aaaaa |
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