Preparation of copper, zinc and aluminum methanol synthesizing catalyst by virtue of reduction deposition method
A methanol synthesis, copper-zinc-aluminum technology, applied in catalyst activation/preparation, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc., can solve problems affecting catalyst activity, copper sintering, etc., to achieve Effects of Small Crystal Size, High Activity, High Methanol Synthesis Performance and Thermal Stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0018] Weigh 22.31g of zinc nitrate hexahydrate and 11.25g of aluminum nitrate nonahydrate and dissolve in 100mL of deionized water, under stirring, add 1mol / L sodium carbonate solution to the above mixed nitrate solution, to pH=7, filter to obtain The filter cake was washed with water to remove Na + , the filter cake was dried at 100 °C, and then calcined at 300 °C for 2 h in an air atmosphere to obtain the carrier ZnO-Al 2 O 3 ; Weigh 4.68g of copper sulfate pentahydrate and dissolve it in 50mL of deionized water, and add it dropwise with 10% ammonia water to obtain a cupro-ammonia solution. At the same time, add water to dilute to 100mL of solution and preheat to 40°C to prepare 70mL of 0.4mol / L hydrazine hydrate. solution and preheated to 40 °C, the carrier ZnO-Al 2 O 3 Disperse in 200mL of 1mol / L sodium hydroxide solution and preheat to 40°C, add cuprammonium solution and hydrazine hydrate solution to 1mol / L sodium hydroxide solution at the same time and stir vigorousl...
Embodiment 2
[0020] Weigh 26.77g of zinc nitrate hexahydrate and 11.25g of aluminum nitrate nonahydrate and dissolve in 100mL of deionized water. Under stirring conditions, add 1mol / L sodium bicarbonate solution to the above mixed nitrate solution to pH=7, filter The obtained filter cake is washed with water to remove Na + , the filter cake was dried at 100 °C, and then calcined at 400 °C for 2 h in an air atmosphere to obtain the carrier ZnO-Al 2 O 3 ; Weigh 18.73g of copper sulfate pentahydrate and dissolve it in 100mL of deionized water, and add it dropwise with 20% ammonia water to obtain a cupro-ammonia solution. At the same time, add water to dilute to 200mL solution and preheat to 50°C, prepare 200mL 3mol / L glucose aqueous solution and preheat it. Heat to 50 °C, the carrier ZnO-Al 2 O 3 Disperse in 200 mL of 1 mol / L sodium hydroxide solution and preheat to 50°C, add cuprammonium solution and hydrazine hydrate solution to 1 mol / L sodium hydroxide solution at the same time and stir...
Embodiment 3
[0022] Weigh 31.24g of zinc nitrate hexahydrate and 11.25g of aluminum nitrate nonahydrate and dissolve in 200mL of deionized water. Under stirring conditions, add 1mol / L sodium hydroxide solution to the above mixed nitrate solution to pH=7, filter The obtained filter cake is washed with water to remove Na + , the filter cake was dried at 100 °C, and then calcined at 300 °C for 2 h in an air atmosphere to obtain the carrier ZnO-Al 2 O 3 ; Weigh 52.43g of copper sulfate pentahydrate and dissolve it in 200mL of deionized water, and add it dropwise with 20% ammonia water to obtain a cupro-ammonia solution. At the same time, add water to dilute to 300mL of solution and preheat to 70°C to prepare 150mL of 2mol / L sodium borohydride aqueous solution. and preheated to 70 °C, the carrier ZnO-Al 2 O 3 Disperse in 200mL of 1mol / L sodium hydroxide solution and preheat to 70°C, add cuprammonium solution and sodium borohydride aqueous solution to 1mol / L sodium hydroxide solution at the s...
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