Bifunctional catalyst as well as preparation and application thereof
A bifunctional catalyst and reaction technology, applied in the direction of electrochemical variables of materials, instruments, measuring devices, etc., can solve the problems of electrochemical quantitative detection and low detection limit of only one substance detected by modified electrodes, and achieve storage stability. Good results with low detection limit and high sensitivity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0043] The preparation of embodiment 1 bifunctional catalyst
[0044] (1) The quality of the three reactants weighed is specifically: weigh 0.1245g Co(CH 3 OO) 2 4H 2 O, 0.062g Ni(CH 3 OO) 2 4H 2 O and 0.114g CH 4 N 2 S in a 50mL beaker;
[0045] (2) The specific preparation method of the reaction solvent is as follows: respectively pipette 8 mL of N,N-dimethylformamide solvent and 8 mL of deionized water into the above-mentioned beaker and stir with a glass rod for 10 minutes to dissolve the reactants;
[0046] (3) The specific method of the reaction step is: move the reaction mixture solution to a 25mL polytetrafluoroethylene autoclave, seal the autoclave and place it in an oven at 200°C for 12 hours of uninterrupted reaction. Wash each with deionized water three times, and use a centrifuge to centrifuge at a speed of 4000r / min to obtain the product. The bifunctional catalyst is obtained. The catalyst is NiCo 2 S 4 / Co 9 S 8 Composition of composite component mat...
Embodiment 2
[0062] Example 2 Preparation of Bifunctional Catalyst Modified Electrode
[0063] (1) Take a glassy carbon electrode with a diameter of 3 mm, wash the glassy carbon electrode with clear water, and in the presence of an appropriate amount of Al with a particle size of 0.05 μm 2 o 3 The powder is ground in a figure 8 manner, polished 50 times, washed with deionized water, then ultrasonically washed with dilute nitric acid, acetone and deionized water, and dried under infrared light to obtain pretreated glassy carbon electrode;
[0064] (2) Get 2mg of the bifunctional catalyst described in Example 1 and disperse it in 2mL Nafion solution by ultrasonic for 20min to obtain the electrode material modification solution. The Nafion solution is dissolved in ethanol and water by Nafion117 film containing 5% (mass percentage) Formed in the mixed solvent (the mass ratio of ethanol and water is 90:10);
[0065] (3) Take 5 μL of the electrode material modification solution and apply it o...
Embodiment 3
[0067] Example 3 Detection Performance of Bifunctional Catalyst Modified Electrode
[0068] In this example, each modified electrode prepared in Example 2 was used as the experimental object, and a three-electrode system was formed with it, a platinum auxiliary electrode, and a saturated calomel reference electrode, and it was connected to a CHI660 electrochemical workstation (Shanghai Chenhua Instrument Co., Ltd.) Electrochemical performance testing.
[0069] (1) Comparison of electrocatalytic oxidation performance of different electrodes for hydrogen peroxide electrocatalytic reduction and levodopa
[0070] In order to more intuitively reflect the electrocatalytic reduction performance of the bifunctional catalyst-modified electrode prepared by the present invention to hydrogen peroxide and the electrocatalytic oxidation performance of levodopa, the glassy carbon electrode (a), the solid microsphere catalyst-modified electrode ( b), flower-shaped microsphere catalyst modifi...
PUM
| Property | Measurement | Unit |
|---|---|---|
| diameter | aaaaa | aaaaa |
| particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com



