Method for preparing mesoporous molecular sieve-loading Cu-Ni bimetallic catalyst
A technology of bimetallic catalysts and mesoporous molecular sieves, applied in molecular sieve catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problems of complex preparation process, poor reproducibility, low selectivity and catalytic activity, and achieve The effect of simple process, strong acid center and good thermal stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0017] Example 1: (1) Add NaOH, aluminum isopropoxide, tetraethylammonium bromide (25%), water glass, copper nitrate and RaneyNi deionized water into the reaction kettle, mechanically stir vigorously to make it a uniform mixed solution, and program the temperature After aging at 140°C for 4 hours. The stoichiometric ratio of the reaction raw materials is Al 2 o 3 / SiO 2 / Na 2 O / (TEA) 2 O / Cu / Ni / H 2 O=0.5 / 55 / 2.0 / 0.5-1.8 / 0.4 / 0.5 / 800.
[0018] (2) Take 4.0g of the solution obtained in step (1), 1.0g of EO20PO70EO20 (P123), 10g of 1-hexadecyl-3-methylimidazolium bromide ionic liquid and 15ml of distilled water, and stir it mechanically to dissolve it. Then control the crystallization conditions (95°C, 23 hours) to adjust the size and purity of the crystal form. The resulting crystals were successively filtered, washed and dried in vacuo.
[0019] (3) Put the raw mesoporous molecular sieve powder obtained in step (2) into a muffle furnace, and bake it at 550°C for 5.5 hours...
Embodiment 2
[0020] Example 2: (1) Add NaOH, aluminum isopropoxide, tetraethylammonium bromide (25%), water glass, copper nitrate and RaneyNi deionized water into the reaction kettle, mechanically stir vigorously to make it a uniform mixed solution, and program the temperature After aging at 140°C for 4 hours. The stoichiometric ratio of the reaction raw materials is Al 2 o 3 / SiO 2 / Na 2 O / (TEA) 2 O / Cu / Ni / H 2 O=1.8 / 65 / 3.0 / 0.5 / 0.4 / 0.5 / 800.
[0021] (2) Take 4.0g of the solution obtained in step (1), 1.0g of EO20PO70EO20 (P123), 10g of 1-hexadecyl-3-methylimidazolium bromide ionic liquid and 15ml of distilled water, and stir it mechanically to dissolve it. Then control the crystallization conditions (95°C, 23 hours) to adjust the size and purity of the crystal form. The resulting crystals were successively filtered, washed and dried in vacuo.
[0022] (3) Put the raw mesoporous molecular sieve powder obtained in step (2) into a muffle furnace, and bake it at 550°C for 5.5 hours to...
Embodiment 3
[0023] Example 3: (1) Add NaOH, aluminum isopropoxide, tetraethylammonium bromide (25%), water glass, copper nitrate and RaneyNi deionized water into the reaction kettle, mechanically stir vigorously to make it a uniform mixed solution, and program the temperature After aging at 140°C for 4 hours. The stoichiometric ratio of the reaction raw materials is Al 2 o 3 / SiO 2 / Na 2 O / (TEA) 2 O / Cu / Ni / H 2 O=1.0 / 60 / 2.5 / 1.2 / 0.4 / 0.5 / 800.
[0024] (2) Take 4.0g of the solution obtained in step (1), 1.0g of EO20PO70EO20 (P123), 10g of 1-hexadecyl-3-methylimidazolium bromide ionic liquid and 15ml of distilled water, and stir it mechanically to dissolve it. Then control the crystallization conditions (95°C, 23 hours) to adjust the size and purity of the crystal form. The resulting crystals were successively filtered, washed and dried in vacuo.
[0025] (3) Put the raw mesoporous molecular sieve powder obtained in step (2) into a muffle furnace, and bake it at 550°C for 5.5 hours to...
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