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Covalent organic framework membranes achieving Mg/Li separation by permeating Mg2+ while retaining Li+
被引:0
|作者:
Liu, Ming
[1
]
Wei, Mingjie
[1
]
Liu, Gan
[1
]
Li, Daiwen
[1
]
Zhang, Zhe
[2
]
Wang, Yong
[1
,3
]
机构:
[1] Nanjing Tech Univ, Coll Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Jiangsu, Peoples R China
[2] Nanjing Tech Univ, Sch Environm Sci & Engn, Nanjing 211816, Jiangsu, Peoples R China
[3] Southeast Univ, Sch Energy & Environm, Nanjing 210096, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Covalent organic framework (COF);
Desalination;
Ion rejection;
Hydrophilicity;
Non-equilibrium molecular dynamics;
simulation;
LITHIUM;
DESALINATION;
PARAMETERS;
ALGORITHMS;
SALT;
D O I:
10.1016/j.memsci.2024.123247
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
Due to the growing demand for lithium in the new energy industry, significant attention has been focused on developing lithium extraction technologies from salt-lake brine. However, the high Mg/Li ratio in salt-lake brine presents challenges for membrane separation technology. If a membrane can allow Mg2+ and water molecules to pass through while retaining Li+, the retained brine will have concentrated Li+ with a reduced Mg/Li ratio, creating the facilitation of further lithium extraction. In this study, we discovered through non-equilibrium molecular dynamics simulations that strongly hydrophilic covalent organic frameworks membranes capture Li+ in their pores, preventing additional Li+ from entering the nanopores. Meanwhile, Mg2+ can freely penetrate these nanopores along with water molecules. This adsorption of Li+ and the free permeation of Mg2+ with water molecules result in the effective separation of Li+ and Mg2+. Consequently, the retained brine becomes lithium-rich with reduced Mg/Li ratio. The findings of this work provide valuable guidance for designing nanofiltration membranes for extracting lithium from salt lakes with high Mg/Li ratio.
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