Preparation method and application of porous carbon @ cobaltosic oxide nanocomposite material
A nanocomposite material and composite material technology, which is applied in the field of preparation of porous carbon@cobalt tetroxide nanocomposite materials, can solve the problems of complex preparation process and unsatisfactory catalytic effect, and achieve a simple synthesis process, regular morphology and easy industrialization. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0025] Example 1 Preparation method of a porous carbon@cobalt tetroxide nanocomposite material
[0026] (1) Under electric stirring, dissolve 17.0 g of acetone and 2.4 mmol of dicyandiamide into a clear solution, add 0.60 g of cobalt nitrate dissolved in an aqueous solution of 8 g of water, cool in an ice bath for 10 min, and stir at 300 rpm At a constant rate, a mixture of 22 mmol toluene diisocyanate and 8 g acetone was added dropwise, the temperature was raised to 30 °C, and the polymerization reaction was kept for 3 h. The obtained solid was dried in an oven at 70 °C to constant weight, and porous Co ( II) - polyphenylurea coordination polymer;
[0027] (2) Put the Co(II)-polyphenylurea coordination polymer in a tube furnace under an air atmosphere at a heating rate of 3°C / min, heat it to 300°C, keep it for 2.5 h, and then heat it at 2°C / min The cooling rate is cooled to room temperature, and the porous carbon @Co 3 o 4 nanocomposites.
Embodiment 2
[0028] Example 2 A preparation method of porous carbon@cobalt tetroxide nanocomposite material
[0029] (1) Under electric stirring, dissolve 17.0 g of acetone and 3.0 mmol of dicyandiamide into a clear solution, add 1.20 g of cobalt nitrate dissolved in an aqueous solution of 12 g of water, cool in an ice bath for 10 min, and then stir at a rate of 300 rpm , add 24mmol of toluene diisocyanate and 10g of acetone dropwise at a constant rate, raise the temperature to 30°C, heat-preserve the polymerization reaction for 3 hours, dry the obtained solid in an oven at 70°C to constant weight, and obtain porous Co(II) - Polyphenylurea coordination polymer;
[0030] (2) Put the Co(II)-polyphenylurea coordination polymer in a tube furnace under an air atmosphere at a heating rate of 5°C / min, heat it to 500°C, keep it for 1.5 h, and then heat it at 2°C / min The cooling rate is cooled to room temperature, and the porous carbon@cobalt tetroxide nanocomposite is prepared.
Embodiment 3
[0031] Example 3 A preparation method of porous carbon@cobalt tetroxide nanocomposite
[0032] (1) Under electric stirring, dissolve 17.0 g of acetone and 2.8 mmol of dicyandiamide into a clear solution, add 0.90 g of cobalt nitrate dissolved in an aqueous solution of 10 g of water, cool in an ice bath for 10 min, and stir at 300 rpm At a constant rate, a mixture of 23mmol toluene diisocyanate and 9 g of acetone was added dropwise, the temperature was raised to 30°C, and the polymerization reaction was kept for 3 h, and the obtained solid was dried in an oven at 70°C to constant weight, and porous Co ( II) - polyphenylurea coordination polymer;
[0033] (2) Put the Co(II)-polyphenylurea coordination polymer in a tube furnace under an air atmosphere at a heating rate of 4 °C / min, heat it to 400 °C, keep it for 2 h, and then heat it at 2 °C / min The cooling rate is cooled to room temperature, and the porous carbon@cobalt tetroxide nanocomposite is prepared.
PUM
| Property | Measurement | Unit |
|---|---|---|
| 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