Method for preparing hexadecyl trimethyl ammonium bromide doped foam nickel catalytic electrode
A technology of cetyl trimethyl ammonium bromide and catalytic electrode, which is applied to electrodes, electrolysis process, electrolysis components, etc., can solve the problems of high price, short electrode service life, poor corrosion resistance, etc., and improve adsorption capacity. , the effect of improving catalytic performance and increasing specific surface area
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] 1) Weigh PdCl 2 Dissolve the powder in 3mol / L HCl solution, add deionized water to prepare 20mmol / L PdCl 2 solution;
[0022] 2) After soaking the nickel foam in 0.5mol / L sulfuric acid for 3 minutes to remove surface matter, it was cleaned by ultrasonic vibration in acetone (degreasing) and double distilled water for 15 minutes respectively, and dried for later use;
[0023] 3) After pyrrole and 0.5mol / l sulfuric acid are mixed in a volume ratio of 7:2493, cetyltrimethylammonium bromide is added to obtain a mixed solution, and the content of cetyltrimethylammonium bromide in the mixed solution 0.0003g / mL;
[0024] 4) With the nickel foam treated in step 2) as the anode, the platinum sheet as the cathode, and the solution prepared in the step 3) as the electrolyte, the PPy-CTAB / nickel foam electrode is obtained by electrodeposition, and the deposition current density 0.56mA / cm 2 , the deposition time is 3min;
[0025] 5) With the PPy-CTAB / nickel foam electrode as th...
Embodiment 2
[0028] 1) Weigh PdCl 2 Dissolve the powder in 3mol / L HCl solution, add deionized water to prepare 24.5mmol / L PdCl 2 solution;
[0029] 2) Soak nickel foam in 0.5mol / L sulfuric acid for 2 minutes to remove surface matter, then ultrasonically shake it in acetone (degreasing) and double-distilled water for 10 minutes to clean it, and dry it for later use;
[0030] 3) After pyrrole and 0.5mol / L sulfuric acid are mixed in a volume ratio of 7:2493, cetyltrimethylammonium bromide is added to obtain a mixed solution, and the content of cetyltrimethylammonium bromide in the mixed solution 0.0003g / mL;
[0031] 4) With the nickel foam treated in step 2) as the anode, the platinum sheet as the cathode, and the solution prepared in the step 3) as the electrolyte, the PPy-CTAB / nickel foam electrode is obtained by electrodeposition, and the deposition current density 0.56mA / cm 2 , the deposition time is 3min;
[0032] 5) With the PPy-CTAB / nickel foam electrode as the cathode, the platin...
Embodiment 3
[0035] 1) Weigh PdCl 2 Dissolve the powder in 3mol / L HCl solution, add deionized water to prepare 25mmol / L PdCl 2 solution;
[0036] 2) Soak nickel foam in 0.5mol / L sulfuric acid for 3 minutes to remove surface matter, then ultrasonically shake in acetone (degreasing) and double-distilled water for 15 minutes to clean it up, and dry it for later use;
[0037] 3) After pyrrole and 0.5mol / L sulfuric acid are mixed in a volume ratio of 7:2493, cetyltrimethylammonium bromide is added to obtain a mixed solution, and the content of cetyltrimethylammonium bromide in the mixed solution 0.0003g / mL;
[0038] 4) With the nickel foam treated in step 2) as the anode, the platinum sheet as the cathode, and the solution prepared in the step 3) as the electrolyte, the PPy-CTAB / nickel foam electrode is obtained by electrodeposition, and the deposition current density 0.56mA / cm 2 , the deposition time is 3min;
[0039] 5) With the PPy-CTAB / nickel foam electrode as the cathode, the platinum...
PUM
Property | Measurement | Unit |
---|---|---|
current density | 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