Method for preparing vanadium sodium phosphate and vanadium phosphate serving as anode material of sodium ion battery
A technology of sodium vanadium phosphate, positive electrode material, applied in battery electrodes, circuits, electrical components and other directions, can solve the problems of cumbersome steps, unfavorable industrial production, complicated operation, etc., and achieves simple process flow, easy industrial production, and shortened process steps. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0019] Preparation vanadium phosphate (VPO) of the present invention 4 ) method includes the following steps:
[0020] The trivalent vanadium source compound is reacted with a base to obtain vanadium hydroxide. Wherein, the trivalent vanadium source compound can be vanadium sulfate (V 2 (SO 4 ) 3 ), vanadium chloride (V 3 Cl 2 ) in one or a combination of two. The alkali used can be one or more combinations of sodium hydroxide, potassium hydroxide, calcium hydroxide, and ammonia. The addition of alkali only needs to make the pH value of the aqueous solution of vanadium sulfate or vanadium chloride be 4-10 to produce vanadium hydroxide precipitation. Precipitated vanadium hydroxide can also be collected. Precipitated vanadium hydroxide can be collected by filtration or centrifugation. The collected vanadium hydroxide can also be washed. Vanadium hydroxide can be washed with water or one or a combination of two or more organic solvents such as methanol, ethanol, aceton...
Embodiment 1
[0028] Weigh 0.05mol (19.5g) vanadium sulfate (V 2 (SO 4 ) 3 ), was added into 100mL deionized water, and ultrasonically dissolved to obtain solution A containing trivalent vanadium ions.
[0029] The pH value of solution A was adjusted to 7 with sodium hydroxide solution (concentration: 10 wt%), and a large amount of precipitate B was produced in solution A.
[0030] Precipitate B was filtered and washed, dissolved in 100 mL of phosphoric acid solution, and refluxed at 100°C for 6 hours under the protection of argon to obtain precipitate C, which was filtered and washed.
[0031] Dry the precipitate C at 40°C for 5 h under vacuum to obtain vanadium phosphate (VPO 4 )solid.
Embodiment 2
[0033] Weigh 0.05mol (7.825g) vanadium trichloride (VCl 3 ), was added into 100mL deionized water, and ultrasonically dissolved to obtain solution A containing trivalent vanadium ions.
[0034] The pH value of solution A was adjusted to 6 with ammonia water (concentration: 10 wt%), and a large amount of precipitate B was produced in solution A.
[0035] Precipitate B was filtered and washed, dissolved in 100 mL of phosphoric acid solution, and refluxed at 120°C for 4 hours under the protection of argon to obtain precipitate C, which was filtered and washed.
[0036] Dry the precipitate C at 60°C for 2 h under vacuum to obtain vanadium phosphate (VPO 4 )solid.
PUM
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