吸附
盐酸四环素
碳化
十二烷基苯
材料科学
咪唑酯
化学
化学工程
比表面积
碳纤维
水溶液
沸石咪唑盐骨架
金属有机骨架
磺酸盐
复合数
无机化学
微型多孔材料
有机化学
四环素
钠
催化作用
复合材料
工程类
抗生素
生物化学
作者
Zhe Zhang,Yi Chen,Peng Wang,Zhen Wang,Can Zuo,Wenqing Chen,Tianqi Ao
标识
DOI:10.1016/j.jhazmat.2021.127103
摘要
N-doped hierarchical porous carbons (NHPCs) were successfully prepared from soft-templated zeolitic imidazolate framework-8 (ZIF-8) precursors using sodium dodecylbenzene sulfonate (SDBS) as a template through facile one-step carbonization and applied in tetracycline hydrochloride (TCH) adsorption. The NHPC synthesized at 1000 °C with an SDBS/Zn2+ molar ratio of 0.075 exhibited the highest TCH adsorption (qm = 80.92 mg g-1) owing to its relatively large BET surface area (1067.41 m2 g-1) and pore volume (1.22 cm3 g-1) and the stronger surface interaction between TCH and NHPCs (HC1000-0.075). Compared with surfactant-free ZIF-8-derived carbon (HC), introduction of SDBS in the ZIF-8 precursor not only improved the pore structure of the carbon materials but also increased the nitrogen content and the number of surface functional groups. Adsorption kinetics and isotherms showed that the pseudo-second-order model and Sips model fit the TCH adsorption behavior on HC and HC1000-0.075 well. Adsorption experiments and characterizations revealed that the adsorption mechanism involved in TCH adsorption on HC1000-0.075 mainly depended on the synergistic effect of pore filling, H-bonding, π-π interactions, and weak electrostatic interactions. This study provides an effective and simple strategy for fabricating MOF-derived NHPCs as a promising adsorbent for the removal of antibiotics from water.
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