环氧氯丙烷
吸附
化学吸附
化学
胍丁胺
水溶液中的金属离子
朗缪尔吸附模型
表面改性
核化学
离子
配体(生物化学)
物理吸附
无机化学
焓
朗缪尔
傅里叶变换红外光谱
化学工程
高分子化学
有机化学
物理化学
腐胺
量子力学
受体
工程类
生物化学
酶
物理
作者
Gülay Bayramoğlu,M. Yakup Arıca
标识
DOI:10.1007/s10967-024-09548-w
摘要
Abstract In the presented work, magnetic alginate (MA) beads were prepared and activated with epichlorohydrin and then functionalized with agmatine ligands (MA-A). The materials were analyzed by FTIR, SEM, XRD, and BET methods. The adsorption capacity of the MA-A for U(VI) was 451.4 mg/g. The Langmuir isotherm model well described the experimental data for the adsorption of U(VI) ions. The second-order kinetic model data proposed that the adsorption of U(VI) ions preferred the chemisorption mechanism. The adsorption enthalpy of the MA-A beads for U(VI) ions was 35.4 kJ/mol. After seven cycles of use, the adsorption capacity of MA-A beads was not significantly changed for U(VI) ions. Finally, the functionalization of MA beads with agmatine ligand can be a good candidate for applications for environmental technologies to remove metal ions.
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