Method for extracting lithium from salt lake brine and preparing aluminum hydroxide simultaneously
A technology for aluminum hydroxide and salt lake brine, which is applied in the preparation of aluminum hydroxide, chemical instruments and methods, separation methods, etc., can solve problems such as air pollution, ion channel blockage, and adsorbent dissolution, and achieve high-efficiency comprehensive utilization and easy scale. The effect of chemical production and small loss of lithium
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0023] A. Using the method introduced in the patent CN 105152193A, weigh MgCl 2 ·6H 2 O 26.0325g, MgSO 4 ·7H 2 O 25.7993g, AlCl 3 ·6H 2 O 18.729g, KCl 3.3873g, LiCl 1.8768g, NaCl 8.068g were dissolved in 250mL deionized water to obtain a salt solution; NaOH 19.8593g, NaCO 3 16. Dissolve 4443g in 250mL deionized water to obtain an alkaline solution; pour the salt solution and the alkaline solution into a colloid mill at the same time, and rotate at a speed of 3000r / min for 3 minutes to form a MgAl-LDH crystal nucleus; transfer the crystal nucleus solution to the reactor, Crystallize under dynamic stirring at 80°C for 12 hours to grow MgAl-LDH; filter to obtain a MgAl-LDH filter cake, and dry the MgAl-LDH filter cake at 70°C for 12 hours to obtain a white solid MgAl-LDH product; collect the filtrate into a container. The filtrate is lithium-containing brine.
[0024] Evaporate and concentrate the lithium-containing brine until the lithium ion concentration reaches 0.4432g...
Embodiment 2
[0030] A. Prepare MgAl-LDH product, collect lithium-containing brine with embodiment 1.
[0031] Evaporate and concentrate the lithium-containing brine until the lithium ion concentration reaches 0.4385g / L, take 1 liter of concentrated lithium-containing solution, add 45.76g of aluminum chloride to prepare a mixed salt solution, and add dropwise a sodium hydroxide solution with a molar concentration of 4mol / L, The dropping rate was 1 mL / min until pH=7, and the reaction was carried out at 80° C. for 12 hours, and the LiAl-LDH filter cake and filtrate were obtained after solid-liquid separation. The filtrate is evaporated and concentrated to a lithium ion concentration of 0.4g / L, and returned to the lithium-containing brine for recycling.
[0032] LiAl-LDH filter cake is lithium-containing layered material LiAl 3 (OH) 9 Cl·5H 2 O, the solid content is 85%.
[0033] B. Disperse 30 g of filter cake with a solid content of 85% in 3 L of aqueous solution adjusted to pH = 6 with ...
Embodiment 3
[0037] A, prepare MgAl-LDH product, collect lithium-containing brine with embodiment 1.
[0038] Evaporate and concentrate the lithium-containing brine until the lithium ion concentration reaches 0.4108g / L, take 1 liter of concentrated lithium-containing solution, add 57.16g of aluminum chloride to prepare a mixed salt solution, and add dropwise a sodium hydroxide solution with a molar concentration of 4mol / L, The dropping rate was 1 mL / min until pH=7, and the reaction was carried out at 80° C. for 12 hours, and the LiAl-LDH filter cake and filtrate were obtained after solid-liquid separation. The filtrate is evaporated and concentrated to a lithium ion concentration of 0.2 g / L, and returned to the lithium-containing brine for recycling.
[0039] LiAl-LDH filter cake is lithium-containing layered material LiAl 4 (OH) 12 Cl 7H 2 O, the solid content is 85%.
[0040] B. Disperse 30 g of filter cake with a solid content of 85% in 3 L of aqueous solution adjusted to pH=5.5 wit...
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