In situ synthetic hierarchical porous MIL-53(Cr) as an efficient adsorbent for mesopores-controlled adsorption of tetracycline

吸附 介孔材料 多孔性 四环素 化学工程 扩散 材料科学 传质 化学 色谱法 有机化学 催化作用 热力学 生物化学 物理 工程类 抗生素
作者
Junhao Yang,Han Lin,Wanyong Yang,Qing Liu,Zhaoyang Fei,Xian Chen,Zhuxiu Zhang,Jihai Tang,Mifen Cui,Xu Qiao
出处
期刊:Microporous and Mesoporous Materials [Elsevier BV]
卷期号:332: 111667-111667 被引量:23
标识
DOI:10.1016/j.micromeso.2021.111667
摘要

Significant concerns have been raised over the adsorption of tetracyclines from aquatic environments. In this paper, hierarchically porous MIL-53(Cr) was synthesized by in situ synthesis for the first time and the influence of mesopores on tetracycline adsorption was investigated. Benefiting from the high mesoporous volume, more TC molecular could enter the channel to interact with adsorption sites, and the adsorption capacity of 20-AA-MIL-53(Cr) for TC increased twelvefold, up to 148.5 mg/g. In addition, various kinetic models have also been used to investigate the adsorption process of tetracycline. Particularly, considering the molecular size of TC about 12.9 Å×7.4 Å, Elovich and intraparticle diffusion kinetic models were used to testify that the external mass transfer of TC on 20-AA-MIL-53(Cr) was much higher than that on MIL-53(Cr) when the pore size was expanded to 2–3 nm. What's more, the results of water stability test revealed the excellent water stability of 20-AA-MIL-53(Cr) for over 5 days. This study described a simple method for the preparation of hierarchical porous MIL-53(Cr) and explored the effect of mesopores on the adsorption of TC, so as to propose that hierarchical porous MIL-53(Cr) can be used as a potential adsorbent in water adsorption treatment. • Hierarchical porous x-AA-MIL-53(Cr) was prepared by in situ synthesis for the first time. • 20-AA-MIL-53(Cr) had the highest surface area (2249 m 2 /g) and mesoporous volume (0.62 cm 3 /g). • The adsorption capacity of tetracycline by hierarchical porous MIL-53(Cr) increased twelvefold. • The presence of mesopores allowed more tetracycline molecules to contact the adsorption sites.
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