三水铝石
插层(化学)
解吸
氢氧化物
吸附
碱度
锂(药物)
铝
离子强度
氢氧化锂
碱金属
萃取(化学)
化学工程
化学
无机化学
离子
色谱法
工程类
有机化学
水溶液
离子交换
医学
内分泌学
作者
Jun Chen,Jianglong Du,Jianguo Yu,Sen Lin
出处
期刊:Desalination
[Elsevier]
日期:2023-05-01
卷期号:554: 116491-116491
被引量:15
标识
DOI:10.1016/j.desal.2023.116491
摘要
Excessive Li+ deintercalation from the difficulty of precisely controlling desorption would lead to the deactivation of lithium/aluminum layered double hydroxide (Li/Al-LDH) as the aluminum-based lithium adsorbent in brines. In this study, a novel one-step regeneration method was established to in-suit recover the deactivated Li/Al-LDH and was verified to be universally applicable for Li/Al-LDH with different forms and deactivation degrees. It was witnessed the powdery and granulated Li/Al-LDH could be regenerated in less than 5 min and 2 h, respectively. The in-situ regeneration of deactivated granules was achieved in the fixed bed. Besides, high temperature, high Li+ concentration, alkalinity, and high ionic strength were conductive to the structural transformation of deactivated adsorbents from gibbsite (γ-Al(OH)3) to active Li/Al-LDH and restore to normal Li+ adsorption capacity on account of the intercalation reaction of Li+ in gibbsite. Moreover, the regeneration mechanism was further illustrated in detail that Cl− and water molecules entered the interlayer as Li+ was inserted into the vacancies of deactivated adsorbent laminates to reconstruct Li/Al-LDH structure. This efficient regeneration method resolves the deactivation of Li/Al-LDH adsorbents, and is expected to be applied in the industrial lithium extraction to completely solve the insufficient long-term cycle stability caused by excessive desorption.
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