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Extraordinary Separation of Acetylene‐Containing Mixtures with Microporous Metal–Organic Frameworks with Open O Donor Sites and Tunable Robustness through Control of the Helical Chain Secondary Building Units
Authors:Zizhu Yao  Prof. Dr. Zhangjing Zhang  Lizhen Liu  Ziyin Li  Prof. Dr. Wei Zhou  Dr. Yunfeng Zhao  Prof. Dr. Yu Han  Prof. Dr. Banglin Chen  Prof. Dr. Rajamani Krishna  Prof. Dr. Shengchang Xiang
Affiliation:1. Fujian Provincial Key Laboratory of Polymer Materials, Fujian Normal University, Fuzhou, P. R. China;2. NIST Center for Neutron Research, Gaithersburg, Maryland, USA;3. Advanced Membranes and Porous Materials Center, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia;4. Institute for New Energy Materials & Low-Carbon Technologies, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin, P. R. China;5. Department of Chemistry, University of Texas at San Antonio, San Antonio, Texas, USA;6. Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Amsterdam, The Netherlands
Abstract:Acetylene separation is a very important but challenging industrial separation task. Here, through the solvothermal reaction of CuI and 5‐triazole isophthalic acid in different solvents, two metal–organic frameworks (MOFs, FJU‐21 and FJU‐22 ) with open O donor sites and controllable robustness have been obtained for acetylene separation. They contain the same paddle‐wheel {Cu2(COO2)4} nodes and metal–ligand connection modes, but with different helical chains as secondary building units (SBUs), leading to different structural robustness for the MOFs. FJU‐21 and FJU‐22 are the first examples in which the MOFs’ robustness is controlled by adjusting the helical chain SBUs. Good robustness gives the activated FJU‐22 a , which has higher surface area and gas uptakes than the flexible FJU‐21 a . Importantly, FJU‐22 a shows extraordinary separation of acetylene mixtures under ambient conditions. The separation capacity of FJU‐22 a for 50:50 C2H2/CO2 mixtures is about twice that of the high‐capacity HOF‐3, and its actual separation selectivity for C2H2/C2H4 mixtures containing 1 % acetylene is the highest among reported porous materials. Based on first‐principles calculations, the extraordinary separation performance of C2H2 for FJU‐22 a was attributed to hydrogen‐bonding interactions between the C2H2 molecules with the open O donors on the wall, which provide better recognition ability for C2H2 than other functional sites, including open metal sites and amino groups.
Keywords:column breakthrough  metal–  organic frameworks  open O donors  selective gas adsorption  structural diversity
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