吸附
纳米孔
螺吡喃
化学
盐(化学)
水溶液中的金属离子
无机化学
解吸
金属有机骨架
选择性吸附
金属
离子交换
分子
离子
有机化学
作者
Yuhang Liu,Yuanjiang Zhao,Liming Jiang
标识
DOI:10.1021/acsanm.3c03172
摘要
Herein, we report a kind of light-responsive metal–organic framework (MOF) adsorption material which was fabricated by covalently immobilizing photoactive spiropyran (SP) molecules onto a chromium(III)-based amino-tagged MIL-101 framework through amide linkages. The photoisomerization of SP moieties endows these materials with the unique feature of reversible binding to metal ions. In the dark, the SP-modified MOFs were capable of adsorbing multiple monovalent and divalent salts from saline water and effectively released the adsorbed ions into water upon exposure to simulated sunlight. The SP-modified MOFs showed excellent salt adsorption capacity, of which the MOF with an SP modification ratio of 39% had an ion uptake of 2.27, 1.72, 1.0, 0.8, and 0.39 mmol g–1 for the monocomponent solutions of LiCl, NaCl, KCl, CaCl2, and MgCl2, respectively. After 10 adsorption–desorption cycles, the regenerated adsorbent still exhibited a higher ion adsorption of 1.27 mmol g–1 for the NaCl solution. This work provides a synthetic strategy for salt adsorption materials with nonchemical regeneration ability, which are promising for water desalination and purification.
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