Cerium-containing silver-based hydrotalcite oxygen reduction catalyst as well as preparation method and application thereof
A hydrotalcite and catalyst technology, applied in the field of cerium-containing silver-based hydrotalcite oxygen reduction catalyst and its preparation, can solve the problems of weakening the catalytic activity and poor catalytic activity of the oxygen reduction electrocatalyst
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0031] The invention provides a preparation method of a cerium-containing silver-based hydrotalcite oxygen reduction catalyst, comprising the following steps:
[0032] 1) mixing water-soluble silver salt, water-soluble zinc salt, water-soluble aluminum salt with alkaline solution and heating to obtain silver-zinc-aluminum hydrotalcite suspension;
[0033] 2) performing solid-liquid separation on the suspension obtained in step 1) to obtain a precipitate;
[0034] 3) mixing the precipitate obtained in step 2) with water, and hydrothermally reacting to obtain silver-zinc-aluminum hydrotalcite nanosheets;
[0035] 4) the silver-zinc-aluminum hydrotalcite nanoplate that described step 3) obtains and Ce(DTPA) 2- The anion exchange solution is anion exchanged to obtain Ce(DTPA) 2- Intercalated silver zinc aluminum hydrotalcite;
[0036] The Ce(DTPA) 2- The anion exchange liquid is obtained by mixing cerium salt solution, DTPA solution and sodium hydroxide solution;
[0037] 5) ...
Embodiment 1
[0065] 1) Add silver nitrate, zinc nitrate and aluminum nitrate to 100ml of water in a molar ratio of 1:1:1 to fully dissolve, add sodium hydroxide and sodium carbonate to 100ml of water in a molar ratio of 1:3 to fully dissolve; The two obtained solutions were mixed, and heated in a water bath at 70° C. for 30 minutes under a stirring condition to obtain a suspension of silver-zinc-aluminum hydrotalcite.
[0066] 2) The silver-zinc-aluminum hydrotalcite suspension is centrifuged to obtain the bottom sediment, and the centrifugal speed is 2000r / min;
[0067] 3) Redisperse the bottom sediment obtained after centrifugation in ultrapure water, transfer it to a 200mL hydrothermal reaction kettle, conduct a hydrothermal reaction at 140°C and 480kPa for 24 hours, filter through a filter membrane, wash, and vacuum dry to obtain particles Uniform white powdery silver-zinc-aluminum hydrotalcite nanosheets (AgZnAl-LDHs);
[0068] 4) Obtain 0.2M by adding NaOH dropwise, 50ml of DTPA (di...
Embodiment 2
[0073] Silver nitrate, zinc nitrate and aluminum nitrate are added to 100ml of water in a molar ratio of 1:1:1 and fully dissolved, and sodium hydroxide and sodium carbonate are added to 100ml of water in a molar ratio of 1:1 to fully dissolve; The two solutions were mixed, and heated in a water bath at 80° C. for 10 minutes with stirring to obtain a suspension of silver-zinc-aluminum hydrotalcite.
[0074] 2) The silver-zinc-aluminum hydrotalcite suspension is centrifuged to obtain the bottom sediment, and the centrifugal speed is 2000r / min;
[0075] 3) Redisperse the bottom sediment obtained after centrifugation in ultrapure water, transfer it to a 200mL hydrothermal reaction kettle, conduct a hydrothermal reaction at 150°C and 400kPa for 10 hours, filter through a filter membrane, wash, and vacuum dry to obtain particles Uniform white powdery silver-zinc-aluminum hydrotalcite nanosheets (AgZnAl-LDHs);
[0076] 4) Obtain 0.2M by adding NaOH dropwise, 50ml of DTPA (diethyltr...
PUM
Property | Measurement | Unit |
---|---|---|
Resistivity | 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