吸附
双金属片
化学工程
化学
咪唑酯
碳纤维
盐酸四环素
多孔性
沸石咪唑盐骨架
热解
金属有机骨架
比表面积
无机化学
金属
材料科学
催化作用
有机化学
复合数
四环素
复合材料
生物化学
抗生素
工程类
作者
Zhe Zhang,Yi Chen,Manni Li,Wenqi Song,Peng Wang,Qingzhe Meng,Xing Chen,Yuzhen Zhao,Wenqing Chen
标识
DOI:10.1016/j.seppur.2023.125898
摘要
Zeolitic imidazolate framework-8 (ZIF-8) is attracting considerable attention as a superior precursor to fabricate efficient carbon-based absorbents for many contaminants. However, most carbon materials still suffer from low-efficiency mass transfer and few active sites. Herein, transition metal/nitrogen-codoped hierarchically porous carbons (MNHCs) were controllably constructed by pyrolysis of soft-templated bimetallic ZIFs to enhance tetracycline hydrochloride (TCH) adsorption. Benefitting from its large specific surface area (920.73 m2 g−1), excellent hierarchical pore structure, high N content and abundant Lewis acid sites, the optimum MNHC (HC1000-Fe2Zn98) obtained at 1000 ℃ and the Fe/(Fe + Zn) molar ratio of 2 % improved the adsorption affinity for TCH and reduced the TCH diffusion resistance compared with other MNHCs, resulting in excellent adsorption of TCH. The synergistic effect of Fe and soft templates (sodium dodecyl benzene sulfonate, SDBS) added to the precursor significantly improved pore structure and enriched adsorption active sites of the derived carbon. The adsorption kinetics and isotherm data fitted well with pseudo-second-order kinetics and the Sips model (qm = 245.6 mg g−1), respectively. Adsorption experiments and characterization analyses suggested various adsorption interactions between TCH and MNHCs via pore fillings, coordination, H-bonding and π-π interactions. This study offers a facile strategy for fabricating hierarchically porous carbon for removing organic contaminants from water.
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