Robust Ultramicroporous Metal-Organic Frameworks with Benchmark Affinity for Acetylene

被引:384
|
作者
Peng, Yun-Lei [1 ]
Pham, Tony [6 ]
Li, Pengfei [4 ]
Wang, Ting [1 ]
Chen, Yao [5 ]
Chen, Kai-Jie [2 ]
Forrest, Katherine A. [6 ]
Space, Brian [6 ]
Cheng, Peng [1 ,3 ]
Zaworotko, Michael J. [2 ]
Zhang, Zhenjie [1 ,3 ,5 ]
机构
[1] Nankai Univ, Coll Chem, Tianjin 300071, Peoples R China
[2] Univ Limerick, Dept Chem Sci, Bernal Inst, Limerick V94 T9PX, Ireland
[3] Nankai Univ, Key Lab Adv Energy Mat Chem MOE, Tianjin 300071, Peoples R China
[4] HBNUST, Dept Chem, Qinhuangdao 066004, Peoples R China
[5] Nankai Univ, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[6] Univ S Florida, Dept Chem, 4202 East Fowler Ave,CHE205, Tampa, FL 33620 USA
基金
美国国家科学基金会; 中国国家自然科学基金; 爱尔兰科学基金会;
关键词
acetylene; gas separation; hydrolytic stability; metal-organic frameworks; ultramicroporous materials; SEPARATION; ADSORPTION; SORPTION; BINDING; C2H2;
D O I
10.1002/anie.201806732
中图分类号
O6 [化学];
学科分类号
0703 ;
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: insitu 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 C2H2/CO2 and C2H2/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.
引用
收藏
页码:10971 / 10975
页数:5
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