Magnetic bifunctional catalyst, preparation method therefor and application of magnetic bifunctional catalyst in methanol catalyzed reaction
A bifunctional catalyst and catalyst technology, which are used in the preparation of carbonyl compounds by oxidation, the preparation of carboxylic acids by oxidation, and the preparation of organic compounds, can solve the problems of low methanol concentration, decreased reaction temperature, and poor control of gas-solid catalytic reaction temperature. , to achieve the effect of improving stability, improving activity, avoiding aggregation and loss
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0026] (1) Weigh 17.6g of FeCl 3 ·6H 2 O was dissolved in 82.4g of deionized water to make a solution, and 3.5g of sodium acetate was weighed and dissolved in 46.5g of ethylene glycol to make a solution, and was added dropwise at a water bath temperature of 30°C under stirring conditions 2 In the protected reactor, after the dropwise addition, the mixed solution was put into an autoclave, crystallized at 180°C for 8 hours, then cooled naturally, washed with deionized water and ethanol three times, and dried in vacuum at 60°C for 8 hours. The obtained magnetic Fe 3 o 4 particles.
[0027] (2) Weigh the obtained magnetic Fe 3 o 4 Add 10.6g of particles into 89.4g of ethanol to make liquid A; weigh 3.6g of Ti(SO 4 ) 2 Dissolve in 46.4g deionized water to make solution B; weigh 0.15g polyethylene glycol (PEG-1500) and dissolve in 49.85g ethanol to make solution C. Under the condition of stirring at 40°C, add liquid B and liquid C to liquid A at the same time. After the dro...
Embodiment 2
[0031] (1) Weigh 17.6g of FeCl 3 ·6H 2 O was dissolved in 82.4g of deionized water to make a solution, and 3.5g of sodium acetate was weighed and dissolved in 46.5g of ethylene glycol to make a solution, and was added dropwise at a water bath temperature of 30°C under stirring conditions2 In the protected reactor, after the dropwise addition, the mixed solution was put into an autoclave, crystallized at 180°C for 8 hours, then cooled naturally, washed with deionized water and ethanol three times, and dried in vacuum at 60°C for 8 hours. The obtained magnetic Fe 3 o 4 particles.
[0032] (2) Weigh the obtained magnetic Fe 3 o 4 Add 10.6g of particles into 89.4g of ethanol to make liquid A; weigh 4.8g of Ti(SO 4 ) 2 Dissolve in 45.2g deionized water to make solution B; weigh 0.2g polyethylene glycol (PEG-1500) and dissolve in 49.8g ethanol to make solution C. Under the condition of stirring at 40°C, add liquid B and liquid C to liquid A at the same time. After the dropwis...
Embodiment 3
[0036] (1) Weigh 21.6g of FeCl 3 ·6H 2 O was dissolved in 78.4g of deionized water to make a solution, and 4.3g of sodium acetate was weighed and dissolved in 45.7g of ethylene glycol to make a solution, which was added dropwise at the temperature of a water bath at 30°C under stirring conditions. 2 In the protected reactor, after the dropwise addition, the mixed solution was put into an autoclave, crystallized at 180°C for 8 hours, then cooled naturally, washed with deionized water and ethanol three times, and dried in vacuum at 60°C for 8 hours. The obtained magnetic Fe 3 o 4 particles.
[0037] (2) Weigh the obtained magnetic Fe 3 o 4 Add 15.0g of granules to 85.0g of ethanol to make liquid A; weigh 6.5g of Ti(SO 4 ) 2 Dissolve in 43.5g deionized water to make solution B; weigh 0.25g polyethylene glycol (PEG-1500) and dissolve in 49.75g ethanol to make solution C. Under the condition of stirring at 40°C, add liquid B and liquid C to liquid A at the same time. After ...
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