Preparation method of solid base catalyst, solid base catalyst and application thereof
A solid base catalyst, metal nitrate technology, applied in the preparation of organic compounds, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problems of low catalytic activity, many side reactions, poor stability, etc., and achieve catalytic activity. High, good stability, improve the effect of dispersion
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0024] A preparation method of solid base catalyst, comprising the following steps:
[0025] 1) Dissolve metal nitrate in deionized water, add ɡ-C under stirring condition 3 N 4 (Graphiticcarbonnitride, graphite-like carbon nitride) or NMC (nitrogen-doped mesoporous carbon material);
[0026] 2) Add ammonia water dropwise to the solution prepared in step 1) at 50-70°C, wash and dry after 1-2 hours, then add it to n-butanol, and stir;
[0027] 3) The product obtained in step 2) is dried at 80-100° C. for 6-12 hours, and then calcined.
[0028] The metal nitrate and ɡ-C 3 N 4 Or the mass ratio of NMC is 5:100~30:100; in the step 2), the concentration of the ammonia water is 0.1mol / l~2mol / l; in the step 2), after adding to n-butanol , stirred, and left to stand until n-butanol volatilizes completely; in the step 3), the roasting temperature is 400-800° C., and the roasting time is 1-10 h; in the step 2), ammonia water is added dropwise until the pH of the solution is 9-12; ...
Embodiment 1
[0032] The preparation method of the solid base catalyst of the present embodiment comprises the following steps:
[0033] 1) Dissolve 10g of sodium nitrate and copper nitrate in 200g of deionized water, and add 90g of ɡ-C under stirring conditions 3 N 4 ;
[0034] 2) The solution prepared in step 1) was added dropwise with diluted 1mol / l ammonia water at 50°C, and the ammonia water was added dropwise until the pH of the solution was 11, washed and dried after 1h, then added to n-butanol, stirred, Leave it to stand until n-butanol volatilizes completely;
[0035] 3) The product obtained in step 2) was dried at 80°C for 12h, and then calcined in a muffle furnace at 500°C for 3h to obtain Na 2 O-CuO / ɡ-C 3 N 4 solid base catalyst.
Embodiment 2
[0037] The preparation method of the solid base catalyst of the present embodiment comprises the following steps:
[0038] 1) Dissolve 10g of calcium nitrate and copper nitrate in 200g of deionized water, add 90g of ɡ-C under stirring conditions 3 N 4 ;
[0039] 2) The solution prepared in step 1) was added dropwise with diluted 0.8mol / l ammonia water at 60°C until the pH of the solution was 10, washed and dried after 1.5h, and then added to n-butanol, Stir and let stand until n-butanol volatilizes completely;
[0040] 3) The product obtained in step 2) was dried at 90°C for 8h, and then calcined in a muffle furnace at 600°C for 3h to obtain CaO-CuO / ɡ-C 3 N 4 solid base catalyst.
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