Porosity Modulation in Two-Dimensional Covalent Organic Frameworks Leads to Enhanced Iodine Adsorption Performance

被引:93
作者
An, Shuhao [1 ]
Zhu, Xiang [2 ,3 ]
He, Yanyan [1 ]
Yang, Lan [1 ]
Wang, Hai [3 ]
Jin, Shangbin [4 ]
Hu, Jun [1 ]
Liu, Honglai [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, Suzhou Res Inst, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[3] Texas A&M Univ, Dept Chem, College Stn, TX 77840 USA
[4] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Minist Educ, Sch Chem & Chem Engn, Luoyu Rd 1037, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGHLY EFFICIENT ENRICHMENT; VOLATILE IODINE; CAPTURE; POLYMER; STORAGE; DESIGN;
D O I
10.1021/acs.iecr.9b00028
中图分类号
TQ [化学工业];
学科分类号
0817 ;
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 degrees 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.
引用
收藏
页码:10495 / 10502
页数:8
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