Huang Lijin, Shen Rujia, Liu Ruiqi, Shuai Qin
Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences (Wuhan), No. 388, Lumo Road, Hongshan District, Wuhan, 430074, PR China.
Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences (Wuhan), No. 388, Lumo Road, Hongshan District, Wuhan, 430074, PR China.
J Hazard Mater. 2020 Jun 15;392:122320. doi: 10.1016/j.jhazmat.2020.122320. Epub 2020 Feb 15.
Covalent organic frameworks (COFs) have attracted tremendous attention due to their excellent performance in wastewater remediation, but their practical application still suffers from various challenges. The development of highly-efficient magnetic COFs along with fast adsorption kinetic and high adsorption capacity is very promising. To achieve the purpose, thiol-functionalized magnetic covalent organic frameworks (M-COF-SH) with abundant accessible chelating sites were designed and synthesized by utilizing disulfide derivative as building blocks and subsequently cutting off the disulfide linkage. After the cutting process, the crystallinity, porosity, superparamagnetism of pristine M-COF are well maintained, and the resultant M-COF-SH turned out to be an effective and selective platform for Hg capture from water. Impressively, the resulting composite exhibited a maximum adsorption capacity of Hg as high as 383 mg g. In addition, it also displays a rapid kinetic, where the adsorption equilibrium can be achieved within 10 min. More importantly, there is no significant loss of its adsorption performance even after recycling 5 times. This work not only offers a reliable platform for wastewater remediation but also provides a conceptual guide to prepare functionalized M-COF composites which cannot be obtained through conventional approaches.
共价有机框架材料(COFs)因其在废水处理方面的优异性能而备受关注,但其实际应用仍面临各种挑战。开发具有快速吸附动力学和高吸附容量的高效磁性COFs非常有前景。为实现这一目的,以二硫衍生物为结构单元,通过切断二硫键设计合成了具有丰富可及螯合位点的巯基功能化磁性共价有机框架材料(M-COF-SH)。切断过程后,原始M-COF的结晶度、孔隙率和超顺磁性得以良好保持,所得的M-COF-SH成为从水中捕获汞的有效且选择性的平台。令人印象深刻的是,所得复合材料对汞的最大吸附容量高达383 mg/g。此外,它还具有快速动力学,10分钟内即可达到吸附平衡。更重要的是,即使循环使用5次后其吸附性能也没有显著损失。这项工作不仅为废水处理提供了一个可靠的平台,还为制备无法通过传统方法获得的功能化M-COF复合材料提供了概念指导。