铀酰
化学
吸附
吸附剂
化学吸附
水溶液
选择性吸附
壳聚糖
无机化学
选择性
朗缪尔吸附模型
环氧氯丙烷
水溶液中的金属离子
核化学
离子
有机化学
催化作用
作者
Nadia H. Elsayed,M. Monier,Raedah A.S. Alatawi,Menier Al‐Anazi,Mody Albalawi,Maher J. Alatawi
标识
DOI:10.1016/j.ijbiomac.2023.124073
摘要
The recovery of uranium from aqueous effluents is very important for both the environment and the future of nuclear power. However, issues of sluggish rates and poor selectivity persist in achieving high-efficiency uranium extraction. In this study, uranyl (UO22+) ions were imprinted on an amino-phenolic chitosan derivative using an ion-imprinting method. First, 3-hydroxy-4-nitrobenzoic acid (HNB) units were joined to chitosan via amide bonding, followed by reducing the -NO2 residues into -NH2. The amino-phenolic chitosan polymer ligand (APCS) was coordinated with UO22+ ions, then cross-linked with epichlorohydrin (ECH), and finally the UO22+ ions were taken away. When compared to non-imprinted sorbent, the resulting UO22+ imprinted sorbent material (U-APCS) recognized the target ions preferentially, allowing for much higher adsorption capacities (qm = 309 ± 1 mg/g) and improved adsorption selectivity for UO22+. The FTIR and XPS analyses supported the pseudo-second-order model's suggestion that chemisorption or coordination is the primary adsorption mechanism by fitting the data well in terms of kinetics. Also, the Langmuir model adequately explained the isotherms, suggesting UO22+ adsorption in the form of monolayers. The pHZPC value was estimated at around 5.7; thus, the optimum uptake pH was achieved between pHs 5 and 6. The thermodynamic properties support the endothermic and spontaneous nature of UO22+ adsorption.
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