乙炔
化学吸附
金属有机骨架
选择性
材料科学
水准点(测量)
化学
傅里叶变换红外光谱
金属
衍射
化学工程
有机化学
催化作用
吸附
工程类
地理
物理
光学
大地测量学
作者
Yun‐Lei Peng,Tony Pham,Pengfei Li,Ting Wang,Yao Chen,Kai‐Jie Chen,Katherine A. Forrest,Brian Space,Peng Cheng,Michael J. Zaworotko,Zhenjie Zhang
标识
DOI:10.1002/anie.201806732
摘要
Highly selective separation and/or purification of acetylene from various gas mixtures is a relevant and difficult challenge that currently requires costly and energy-intensive chemisorption processes. Two ultramicroporous metal-organic framework physisorbents, NKMOF-1-M (M=Cu or Ni), offer high hydrolytic stability and benchmark selectivity towards acetylene versus several gases at ambient temperature. The performance of NKMOF-1-M is attributed to their exceptional acetylene binding affinity as revealed by modelling and several experimental studies: in situ single-crystal X-ray diffraction, FTIR, and gas mixture breakthrough tests. NKMOF-1-M exhibit better low-pressure uptake than existing physisorbents and possesses the highest selectivities yet reported for C2 H2 /CO2 and C2 H2 /CH4 . The performance of NKMOF-1-M is not driven by the same mechanism as current benchmark physisorbents that rely on pore walls lined by inorganic anions.
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