Collaborative Innovation Center for Advanced Nuclear Energy Technology, INET, Tsinghua University, Beijing 100084, China.
School of Environment & Natural Resources, Renmin University of China, Beijing 100872, China.
J Hazard Mater. 2020 Mar 5;385:121596. doi: 10.1016/j.jhazmat.2019.121596. Epub 2019 Nov 5.
Covalent organic frameworks (COFs) are emerging and promising adsorbents for the adsorptive removal of many types of pollutants. However, most COFs fabricated by various methods are in the form of microcrystalline powders, making them difficult in separation. In this study, magnetic COFs were prepared by a simple impregnation method. The as-prepared samples with Ms = 5.2 emu g showed a good magnetic separation capability. Additionally, the adsorption performance of magnetic COFs towards antibiotics (e.g., diclofenac and sulfamethazine) was also studied. Various adsorption kinetic models (e.g., the pseudo first-order, the pseudo second-order, and mixed-order models) and adsorption isotherm models (e.g., the Freundlich, the Langmuir, and the Sips models) were used to study their adsorption kinetics and isotherms. Furthermore, density functional theory (DFT) was utilized to predict the interaction between adsorbents and adsorbates and to explain the partial adsorption mechanisms.
共价有机框架(COFs)是一种新兴的、有前途的吸附剂,可用于吸附去除多种类型的污染物。然而,大多数通过各种方法制备的 COFs 呈微晶粉末形式,难以分离。在这项研究中,通过简单的浸渍法制备了磁性 COFs。所制备的 Ms=5.2 emu g 的样品表现出良好的磁分离性能。此外,还研究了磁性 COFs 对抗生素(如双氯芬酸和磺胺甲恶唑)的吸附性能。使用各种吸附动力学模型(如伪一阶、伪二阶和混合阶模型)和吸附等温线模型(如 Freundlich、Langmuir 和 Sips 模型)来研究它们的吸附动力学和等温线。此外,还利用密度泛函理论(DFT)来预测吸附剂和吸附质之间的相互作用,并解释部分吸附机制。