吸附
金属有机骨架
烟气
镍
材料科学
金属
分子
化学工程
配体(生物化学)
氢
氢键
吡啶
有机分子
天然气
无机化学
化学
有机化学
冶金
受体
工程类
生物化学
作者
Yongwei Chen,Houxiao Wu,Daofei Lv,Wenyuan Yang,Zhiwei Qiao,Zhong Li,Qibin Xia
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2018-07-25
卷期号:32 (8): 8676-8682
被引量:36
标识
DOI:10.1021/acs.energyfuels.8b02287
摘要
Metal–organic frameworks hold a great potential for selective CO2 capture to mitigate massive CO2 emission. In this work, we report a nickel-based metal–organic framework, Ni-4PyC, with narrow and uniform ultramicropores of 6.8 Å, exhibiting the CO2 adsorption capacity of 3.11 mmol/g at 298 K and 100 kPa and high CO2/N2 (0.15:0.85) and CO2/CH4 (0.5:0.5) selectivities of 51 and 6, respectively. Meanwhile, its dynamic separation performance is also confirmed by breakthrough experiments of the CO2/N2 and CO2/CH4 mixtures, further demonstrating that Ni-4PyC can selectively capture CO2 from flue gas and remove CO2 from natural gas. Molecular simulation reveals that CO2 molecules are close to the organic ligand of Ni-4PyC (pyridine), leading to CO2 being caught in the middle by two pyridines like a plier via hydrogen bonds. Besides, Ni-4PyC has an excellent recyclability without noticeable loss in CO2 adsorption after five consecutive cycles of static and dynamic adsorption experiments. These combinational merits make Ni-4PyC as an excellent adsorbent for related CO2 capture from flue gas as well as natural gas upgrading.
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