吸附
水溶液
X射线光电子能谱
金属有机骨架
溴化物
朗缪尔吸附模型
傅里叶变换红外光谱
无机化学
密度泛函理论
化学
离子交换
金属
材料科学
化学工程
物理化学
离子
有机化学
计算化学
工程类
作者
Xiaoxin Wang,Dongmei Xu,Dongsheng Yu,Liang Jin,Xiangfeng Liang,Qinghui Shou
标识
DOI:10.1016/j.jece.2023.111600
摘要
The efficient recovery of bromide ions (Br−) from aqueous solutions can alleviate the shortage of bromide resources and holds significant practical value. In this work, an Fe-doped Zr-based metal-organic framework (Fe-MOF-808) was successfully prepared, demonstrating remarkable efficacy in the high-capacity adsorption of Br−. The incorporation of Fe leads to reduction in particle size, elevation of specific surface area, and defect-rich structure, allowing Fe-MOF-808 to quickly adsorb Br−, and the adsorption process follows the Langmuir isotherm and pseudo-second-order kinetic model. Notably, under the conditions of an initial Br− concentration of 100 mg/L, 298 K and pH of 7, Fe-MOF-808 demonstrates exceptional adsorption capacity for Br− (247 mg/g), surpassing that of the pristine MOF-808 and the majority of previously reported adsorbents. Additionally, insights derived from Fourier transform infrared spectrometer (FT-IR), X-ray photoelectron spectroscopy (XPS), and density functional theory (DFT) calculations elucidate the Br− adsorption mechanism on Fe-MOF-808, which can be attributed to the robust interaction between M-OH (M = Zr, Fe) groups and Br−, enhanced electron transfer behavior subsequent to iron modification, and ligand exchange processes. In summary, Fe-MOF-808 emerges as an efficient adsorbent for capturing Br− from aqueous solution, providing a novel approach for the design of advanced Br− adsorbents.
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