MoS2/NiO hollow microsphere material as well as preparation method and application thereof
A hollow microsphere and microsphere technology, applied in chemical instruments and methods, chemical/physical processes, adsorbed water/sewage treatment, etc., can solve the problems of complex preparation process, few active sites, small specific surface area, etc. Simple process, improved catalytic performance, high catalytic activity effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0027] (1) Dissolve 0.32g coconut oil alcohol, 1.4g nickel nitrate hexahydrate, and 0.5403 urea in 225ml deionized water, and stir for 30 minutes to dissolve them all.
[0028] (2) Transfer 40ml of the mixed solution obtained in step (1) to the lining of the hydrothermal reaction kettle, and react at 160°C for 24h.
[0029] (3) Wash the product obtained in step (2) with deionized water and ethanol several times, collect the product, and dry it at 80°C for 24 hours to obtain a precursor.
[0030] (4) The precursor obtained in step (3) was sintered at 300 °C for 2 h in an air atmosphere to obtain pure NiO ultrathin nanosheets.
[0031] (5) Dissolve 1mmol ammonium molybdate and 2mmol thiourea in a mixed solution of 30mL ethylenediamine, 8mL ethylene glycol and 2ml, add 0.30g NiO ultra-thin nanosheets, stir at room temperature for 30min, and react the resulting mixed solution at 180°C for 24h. Washing and drying to obtain MoS 2 / NiO hollow microspheres.
[0032] MoS prepared ab...
Embodiment 2
[0038] (1) Dissolve 0.5g coconut oil alcohol, 2g nickel nitrate hexahydrate, and 0.6 urea in 180ml deionized water, and stir for 30 minutes to dissolve them all.
[0039] (2) Transfer 40ml of the mixed solution obtained in step (1) to the lining of the hydrothermal reaction kettle, and react at 180°C for 24h.
[0040] (3) Wash the product obtained in step (2) with deionized water and ethanol several times, collect the product, and dry it at 80°C for 24 hours to obtain a precursor.
[0041] (4) The precursor obtained in step (3) was sintered at 250°C for 2h in an air atmosphere to obtain pure NiO ultrathin nanosheets.
[0042] (5) Dissolve 1mmol ammonium molybdate and 5mmol thiourea in a mixed solution of 20mL ethylenediamine, 10mL ethylene glycol and 5ml, add 0.04g NiO ultra-thin nanosheets, stir at room temperature for 30min, and react the resulting mixed solution at 180°C for 24h. Washing and drying to obtain MoS 2 / NiO hollow microspheres.
[0043] MoS prepared above 2 ...
Embodiment 3
[0049] (1) Dissolve 0.5g coconut oil alcohol, 2g nickel nitrate hexahydrate, and 0.6 urea in 180ml deionized water, and stir for 30 minutes to dissolve them all.
[0050] (2) Transfer 40ml of the mixed solution obtained in step (1) to the lining of the hydrothermal reaction kettle, and react at 180°C for 24h.
[0051] (3) Wash the product obtained in step (2) with deionized water and ethanol several times, collect the product, and dry it at 80°C for 24 hours to obtain a precursor.
[0052] (4) The precursor obtained in step (3) was sintered at 250°C for 2h in an air atmosphere to obtain pure NiO ultrathin nanosheets.
[0053] (5) Dissolve 1mmol ammonium molybdate and 5mmol thiourea in a mixed solution of 20mL ethylenediamine, 10mL ethylene glycol and 5ml, add 0.08g NiO ultra-thin nanosheets, stir at room temperature for 30min, and react the resulting mixed solution at 180°C for 24h. Washing and drying to obtain MoS 2 / NiO hollow microspheres.
[0054] MoS prepared above 2 ...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | aaaaa | aaaaa |
thickness | aaaaa | aaaaa |
size | 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