共 73 条
Selective biosorption of Li+ in aqueous solution by lithium ion-imprinted material on the surface of chitosan/attapulgite
被引:2
作者:

Xu, Jiaqi
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h-index: 0
机构:
Cent South Univ, Sch Minerals Proc & Bioengn, Changsha 410000, Peoples R China Cent South Univ, Sch Minerals Proc & Bioengn, Changsha 410000, Peoples R China

Chen, Pan
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h-index: 0
机构:
Sichuan Univ, Coll Mat Sci & Engn, Chengdu 610064, Peoples R China Cent South Univ, Sch Minerals Proc & Bioengn, Changsha 410000, Peoples R China
机构:
[1] Cent South Univ, Sch Minerals Proc & Bioengn, Changsha 410000, Peoples R China
[2] Sichuan Univ, Coll Mat Sci & Engn, Chengdu 610064, Peoples R China
基金:
湖南省自然科学基金;
中国国家自然科学基金;
关键词:
Attapulgite;
Ion-imprinted materials;
lithium-ion sieve;
SALT-LAKE BRINES;
CHITOSAN;
RECOVERY;
ADSORPTION;
EXTRACTION;
COMPOSITE;
URANIUM(VI);
SEPARATION;
BATTERIES;
PERFORMANCE;
D O I:
10.1016/j.ijbiomac.2024.133150
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The extraction of Li+ from liquid lithium resources is a pivotal focus of current research endeavors. Attapulgite (ATP), characterized by its distinctive layered structure and inherent ion exchange properties, emerges as an exceptional material for fabricating lithium-ion sieve. Ion-imprinted chitosan/ATP composite materials are successfully synthesized, demonstrating efficacy in selectively absorbing Li+. The results emphasize the rich functional groups present in H-CTP-2, enhancing its absorbability and selectivity, with an adsorption capacity of 37.56 mg center dot g(-1). The adsorption conforms to the Langmuir and pseudo-second-order kinetic model. Li+ coordination involves amino and hydroxyl group, indicating a chemisorption process. Furthermore, the substantial pore structure and significant specific surface area of ATP significantly promote Li+ adsorption, suggesting its participation not only in chemisorption but also in physical adsorption. The fabricated ion-imprinted materials boast substantial adsorption capacity, exceptional selectivity, and rapid kinetics, highlighting their potential for effectively separating Li+ from aqueous solution.
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页数:11
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Univ Cadi Ayyad, Lab Geosci & Environm, Fac Sci & Tech Gueliz, Marrakech, Morocco Univ Cadi Ayyad, Lab Geosci & Environm, Fac Sci & Tech Gueliz, Marrakech, Morocco

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El Ouahabi, M.
论文数: 0 引用数: 0
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机构:
Univ Liege, Dept Geol, Unite Rech Argiles, Geochim & Environm Sedimentaires AGEs, Liege, Belgium Univ Cadi Ayyad, Lab Geosci & Environm, Fac Sci & Tech Gueliz, Marrakech, Morocco

Rhouta, B.
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Univ Cadi Ayyad, Lab Matiere Condensee & Nanostruct, Fac Sci & Tech Gueliz, Marrakech, Morocco Univ Cadi Ayyad, Lab Geosci & Environm, Fac Sci & Tech Gueliz, Marrakech, Morocco

Rocha, F.
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Univ Aveiro, P-3810 Aveiro, Portugal Univ Cadi Ayyad, Lab Geosci & Environm, Fac Sci & Tech Gueliz, Marrakech, Morocco

Fagel, N.
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Univ Liege, Dept Geol, Unite Rech Argiles, Geochim & Environm Sedimentaires AGEs, Liege, Belgium Univ Cadi Ayyad, Lab Geosci & Environm, Fac Sci & Tech Gueliz, Marrakech, Morocco