期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 49, 页码 17743-17746出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b10323
关键词
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资金
- National RD Program [NRF-2016-M1A7A1A02005285]
- National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning [NRF-2016R1C1B1007364, NRF-2016R1A5A1009405, NRF-2017R1A2B4008757]
- Global PhD Fellowship [NRF-2014H1A2A1020670]
Breathing of MIL-53(Al), a flexible metal organic framework (MOF), leads to dynamic changes as narrow pore (np) transitions to large pore (lp). During the flexible and reversible transition, the pore apertures are continuously adjusted, thus providing the tremendous opportunity to separate mixtures of similar-sized and similar-shaped molecules that require precise pore tuning. Herein, for the first time, we report a strategy for effectively separating hydrogen isotopes through the dynamic pore change during the breathing of MIL-53(Al), a representative of flexible MOFs. The experiment shows that the selectivity for D-2 over H-2 is strongly related to the state of the pore structure of MIL-53(Al). The highest selectivity (S-D2/H2 = 13.6 at 40 K) was obtained by optimizing the exposure temperature, pressure, and time to systematically tune the pore state of MIL-53(Al).
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