Method for extracting vanadium and chromium from vanadium chromate mixed solution
A technology of mixed solution and vanadium chromate, which is applied in the field of chemical metallurgy, can solve the problems of low efficiency of vanadium and chromium separation and recovery, complex process, high processing cost, etc., to avoid dangerous solid waste and ammonia nitrogen wastewater, high metal recovery rate, The effect of reducing processing costs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0031] Take 1.5m of vanadium extraction purification solution containing V 45.8g / L and Cr 2.7g / L with pH 8.3 3, Freeze and crystallize at -5°C for 3.5 hours, filter to obtain sodium vanadate crystals and its crystallization mother liquor; the sodium vanadate crystals are dried and dehydrated and sold as products, and the crystallization mother liquor is added to oxidize according to twice the theoretical amount of calcium vanadate precipitation formed by the residual vanadium in it Calcium, ball milled at room temperature for 2 hours, filtered to obtain vanadium removal slag and vanadium removal solution; vanadium removal slag was stirred and added to dilute sulfuric acid, and the pH of the solution was controlled to be 3.5-4.5 to leach vanadium, and the vanadium removal solution was acidified with sulfuric acid to pH 3.6. Then add copper sulfate crystals by stirring 1.5 times of the theoretical amount of copper chromate formed by the chromium therein, after the copper sulfate ...
Embodiment 2
[0033] Take 5000ml of leaching solution obtained from vanadium-chromium reduction slag containing V 13.8g / L and Cr 29.6g / L with pH 11.5, sodium roasting-water immersion, after purification and impurity removal, stir and add sulfuric acid to acidify to pH 1.8, and hydrolyze at 98°C Precipitate vanadium for 2 hours, filter to obtain red vanadium filter cake and liquid after vanadium precipitation; red vanadium filter cake is added to 150g / L ammonium sulfate solution at a liquid-solid ratio of 3:1, adjust the pH to 2.0 with sulfuric acid, and stir at 50°C for 1.5h Wash and remove the sodium, and the red cake after removing the sodium is calcined at 580°C for 3 hours to obtain vanadium pentoxide with a purity of 99.26%. Add sodium hydroxide to adjust the pH to 3.8, and filter to obtain the vanadium-removing slag and the solution after vanadium removal; the vanadium-removing slag is washed with sodium roasting water immersion solution to recover the vanadium in it, and the vanadium-...
Embodiment 3
[0035] Take 1.5m of vanadium extraction solution containing V 25.7g / L and Cr 7.8g / L with pH 9.1 3 , add calcium hydroxide according to 1.3 times of the stoichiometric number of vanadium forming calcium vanadate, stir and ball mill at room temperature for 1.5h, filter to obtain vanadium-precipitated liquid containing V0.03g / L and vanadium-enriched slag containing Cr﹤0.05% . The obtained vanadium-enriched slag was added with water at a solid-to-liquid ratio of 1:3g / ml, and 2mol / L H 2 SO 4 , react at 70°C for 1.5h, control the end point pH value to 3.2, and filter to obtain a vanadium-enriched solution, add ammonium to precipitate vanadium at a mass ratio of ammonium sulfate / vanadium pentoxide to the obtained vanadium-enriched solution, and add sulfuric acid to adjust the pH to 2.0, stirred at 95°C for 1.5h, filtered ammonium polyvanadate, and calcined at 600°C for 1.5h to obtain a vanadium pentoxide product with a purity of 98.6%. After the vanadium precipitation, the liquid ...
PUM
Property | Measurement | Unit |
---|---|---|
concentration | 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