化学
共价键
共价有机骨架
路易斯酸
微型多孔材料
吸附
介孔材料
解吸
无机化学
多孔性
氨
介孔二氧化硅
化学工程
基础(拓扑)
有机化学
催化作用
数学分析
工程类
数学
作者
Christian J. Doonan,David J. Tranchemontagne,T. Grant Glover,Joseph R. Hunt,Omar M. Yaghi
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2010-02-07
卷期号:2 (3): 235-238
被引量:900
摘要
Covalent organic frameworks (COFs) are porous crystalline materials composed of light elements linked by strong covalent bonds. A number of these materials contain a high density of Lewis acid boron sites that can strongly interact with Lewis basic guests, which makes them ideal for the storage of corrosive chemicals such as ammonia. We found that a member of the covalent organic framework family, COF-10, shows the highest uptake capacity (15 mol kg⁻¹, 298 K, 1 bar) of any porous material, including microporous 13X zeolite (9 mol kg⁻¹), Amberlyst 15 (11 mol kg⁻¹) and mesoporous silica, MCM-41 (7.9 mol kg⁻¹). Notably, ammonia can be removed from the pores of COF-10 by heating samples at 200°C under vacuum. In addition, repeated adsorption of ammonia into COF-10 causes a shift in the interlayer packing, which reduces its apparent surface area to nitrogen. However, owing to the strong Lewis acid-base interactions, the total uptake capacity of ammonia and the structural integrity of the COF are maintained after several cycles of adsorption/desorption.
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