Si-Fe/gamma-Al2O3 catalyst and preparation method thereof
A catalyst and co-catalyst technology, applied in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problem of low catalytic activity, difficulty in rapid and efficient oxidation and degradation of phenolic pollution It can achieve high catalytic activity, good catalytic oxidation effect, and the effect of reducing activation energy
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0037] The Si-Fe / γ-Al of this example 2 o 3 The preparation method of catalyst comprises the following steps:
[0038] S1: crushing the boehmite into particles with a particle size ranging from 0.250 to 0.425 mm to obtain boehmite powder for later use;
[0039] S2: The boehmite powder is heated up to 550-650°C at a rate of 5-10°C / min, and heated at a constant temperature for 3-6 hours to prepare γ-Al 2 o 3 Powder;
[0040] S3: Dissolve the structure directing agent in deionized water, then add Fe(NO 3 ) 3 9H 2 O, stir until completely dissolved, then add tetraethylorthosilicate dropwise, and stir evenly to obtain a mixed solution; the structure-directing agent includes polyethylene glycol, cetyltrimethylammonium bromide, One or more of block copolymer P123 and triblock copolymer F127;
[0041] S4: to γ-Al 2 o 3 Add the mixed solution obtained by adding S3 dropwise to the powder, and stir and react at 25°C for 6-18 hours to obtain a catalyst precursor; the structure-d...
Embodiment 1
[0043] Embodiment 1 prepares Si 0.05 -Fe / γ-Al 2 o 3 catalyst
[0044] S1: crushing the boehmite into particles with a particle size ranging from 0.250 to 0.425 mm to obtain boehmite powder for later use;
[0045] S2: The boehmite powder is heated up to 550°C at a rate of 5°C / min, and heated at a constant temperature for 3 hours to prepare γ-Al 2 o 3 Powder;
[0046] S3: Dissolve 0.1g cetyltrimethylammonium bromide in 4mL deionized water, then add 3.6173g Fe(NO 3 ) 3 9H 2 O, after stirring until completely dissolved, add 0.1854g tetraethyl orthosilicate dropwise, after stirring evenly, a mixed solution is obtained;
[0047] S4: to 5.0g γ-Al 2 o 3 The mixed solution obtained by adding S3 dropwise to the powder was stirred and reacted at 25°C for 12 hours to obtain a catalyst precursor;
[0048] S5: Dry the catalyst precursor at 120°C, move it into a crucible and cover it, put it into a muffle furnace, bake it at 500°C for 4 hours, and cool it to room temperature at 25...
Embodiment 2
[0049] Embodiment 2 prepares Si 0.10 -Fe / γ-Al 2 o 3 catalyst
[0050] S1: crushing the boehmite into particles with a particle size ranging from 0.250 to 0.425 mm to obtain boehmite powder for later use;
[0051] S2: The boehmite powder is heated up to 600°C at a rate of 5°C / min, and heated at a constant temperature for 4 hours to prepare γ-Al 2 o 3 Powder;
[0052] S3: Dissolve 0.1g polyethylene glycol 4000 in 4mL deionized water, then add 3.6173gFe(NO 3 ) 3 9H 2 O, after stirring until completely dissolved, add 0.3709g tetraethyl orthosilicate dropwise, after stirring evenly, a mixed solution is obtained;
[0053] S4: to 5.0g γ-Al 2 o 3 The mixed solution obtained by adding S3 dropwise to the powder was stirred and reacted at 25°C for 12 hours to obtain a catalyst precursor;
[0054] S5: Dry the catalyst precursor at 120°C, move it into a crucible and cover it, put it into a muffle furnace, bake it at 500°C for 4 hours, and cool it to room temperature at 25°C natu...
PUM
Property | Measurement | Unit |
---|---|---|
Particle size | 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