海水
吸附
铀
铀酰
解吸
萃取(化学)
化学
朗缪尔吸附模型
化学工程
可重用性
核化学
无机化学
色谱法
材料科学
有机化学
冶金
海洋学
工程类
地质学
软件
计算机科学
程序设计语言
作者
Jiajia Yang,Yun Li,Tian Tian,Haitao Shi,Zia Ahmad,Ningbo Geng,Jing Jin,Yanqiang Huang,Haijun Zhang,Hongjun Fan,Jiping Chen
标识
DOI:10.1016/j.cej.2023.142952
摘要
According to the global vision of “carbon peak and carbon neutrality”, extracting uranium from natural seawater is regarded as a promising candidate for meeting nuclear fuel demand. Nevertheless, owing to the very low uranium concentration and complexity of natural seawater, the development of adsorbent materials for extracting uranium from seawater with satisfactory efficiencies remains a great challenge. In this work, we for the first time developed a novel mesocellular silica foam (MSF) supported hyperbranched poly(amidoxime-ethyleneimine) (PAO-PEI) network ([email protected]). After systematic evaluation, the [email protected] exhibited high adsorption capacity and excellent reusability, fast adsorption kinetics as well as good adsorption selectivity and affinity towards uranyl ions, simultaneously. Besides the obtained short equilibrium time of ∼ 20 h, the [email protected] achieved a remarkable adsorption capacity of 926.2 mg-U/g-Ads. for 100 mg/L of uranium water solution. Meanwhile, the [email protected] showed evident higher selectivity towards uranium (29.3 mg g−1) against vanadium (7.2 mg g−1) and other coexisting metal ions in simulated seawater. Moreover, excellent reusability of [email protected] in eight consecutive adsorption–desorption cycles was also observed. More importantly, satisfactory extraction efficiencies (90.6–92.9 %) for U-spiked real seawater was obtained in 48 h. Finally, a uranium adsorption capacity of 1.102 mg g−1 for coastal seawater in 20 days was obtained. All these findings demonstrate the relatively good potential of [email protected] for extracting uranium from real seawater.
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