Multipurpose Metal-Organic Framework for the Adsorption of Acetylene: Ethylene Purification and Carbon Dioxide Removal

被引:113
|
作者
Qazvini, Omid T. [1 ]
Babarao, Ravichandar [2 ,3 ]
Telfer, Shane G. [1 ]
机构
[1] Massey Univ, MacDiarmid Inst Adv Mat & Nanotechnol, Inst Fundamental Sci, Palmerston North 4442, New Zealand
[2] RMIT Univ, Sch Sci, Melbourne, Vic 3001, Australia
[3] Commonwealth Sci & Ind Res Org CSIRO Mfg, Clayton, Vic 3169, Australia
基金
澳大利亚研究理事会;
关键词
SELECTIVE HYDROGENATION; EFFICIENT SEPARATION; C2H2/CO2; MIXTURES; CO2; BINDING; SITES;
D O I
10.1021/acs.chemmater.9b01691
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The separation of acetylene, ethylene, and carbon dioxide is a great challenge in view of their similar sizes and physical properties. Recently, adsorptive separations using porous metal-organic frameworks have risen to prominence. Here, we report a novel microporous metal-organic framework, termed MUF-17, that selectively adsorbs acetylene in the presence of ethylene or carbon dioxide. MUF-17 possesses one-dimensional zig-zag pores that are lined with amino and carboxylate groups, and coordinated water molecules. This pore surface is highly polar and has appropriate dimensions to interact optimally with guest acetylene molecules. Dispersion-corrected density functional theory calculations confirm the strong interactions between the framework and acetylene and illustrate the electrostatic basis for its lower affinity for other gases. The application of MUF-17 to gas separations was demonstrated by dynamic breakthrough measurements. It is a multipurpose adsorbent, removing trace quantities of acetylene from ethylene and sequestering bulk quantities in the presence of carbon dioxide. Its excellent performance fruitfully couples high selectivity with uptake capacity. Advantageously, MUF-17 is straightforward, robust, and inexpensive to prepare. Its recyclability and high stability render it a high-performance material for sustainable and energy efficient separation processes.
引用
收藏
页码:4919 / 4926
页数:8
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