多孔性
吸附
共价键
共价有机骨架
化学工程
材料科学
纳米技术
碘
化学
有机化学
复合材料
工程类
作者
Shuhao An,Xiang Zhu,Yanyan He,Lan Yang,Hai Wang,Shangbin Jin,Jun Hu,Honglai Liu
标识
DOI:10.1021/acs.iecr.9b00028
摘要
Covalent organic frameworks (COFs) with atomically precise integration of scaffolds into 2D/3D topologies have shown great promise for separation applications. In this work, a porosity modulation approach was developed for the construction of 2D COFs for efficient volatile iodine adsorption. By rationally turning building blocks, significantly different iodine separation performance was obtained on COFs, where the best COF adsorbent exhibits a high-performance volatile iodine uptake of 4.0 g g–1 at 75 °C and under ambient pressure and full pore access of iodine was achieved. Most importantly, the separation experiments reveal that iodine uptake capacities on COFs are not only determined by their pore volumes but also significantly affected by their intrinsic pore sizes. Both should be regulated simultaneously to work in concert when designing new COFs for the capture of volatile iodine.
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