吸附
介孔材料
金属有机骨架
原位
无定形固体
配体(生物化学)
化学工程
金属
选择性
材料科学
无机化学
化学
有机化学
催化作用
工程类
生物化学
受体
作者
Wenyu Li,Zhen Chen,Li Yang,Yuan-Hang Qin,Tielin Wang,Wei Sun,Cunwen Wang
标识
DOI:10.1016/j.ces.2024.119797
摘要
In this study, a transformative shift from amorphous to crystalline MOFs was achieved by altering the input sequence of organic ligands, metal sources, and HCl while minimizing the usage of HCl. By adjusting the ratio of HCl, various degrees of ligand and cluster deletions occurred, facilitating precise control over mesopore size from range of 2–5 to 18–31 nm. The experiments demonstrate that the synthesized materials exhibit outstanding pH adsorption capabilities within the range of pH 1 to 10. Particularly noteworthy is the performance of Zr-PDC-20, which displayed excellent equilibrium and maximum adsorption capacities, measuring 210 mg/g and 423 mg/g respectively at pH 7. Importantly, even in solutions containing diverse anions such as NO-3, SO2-4, COOH–, Cl−, and CO2-3, the material exhibited exceptional anti-interference capacities. Consequently, these adsorbents have good adsorption capacity, selectivity, and a broad pH range, enabling the effective and rapid removal of Gly from complex water environments.
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