4.8 Article

A chemically stable nanoporous coordination polymer with fixed and free Cu2+ ions for boosted C2H2/CO2 separation

期刊

NANO RESEARCH
卷 14, 期 2, 页码 546-553

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-020-2935-1

关键词

nanoporous coordination polymer; high porosity; new topology; post-synthetic approach; C2H2/CO2 separation

资金

  1. National Natural Science Foundation of China [21671102, 21973029]
  2. Innovative Research Team Program by the Ministry of Education of China [IRT-17R54]
  3. Hunan Provincial Natural Science Foundation of China [2020JJ4290]
  4. Young and Middle-aged Academic Leader of Jiangsu Provincial Blue Project
  5. Six Talent Peaks Project in Jiangsu Province [JY-030]
  6. State Key Laboratory of Materials-Oriented Chemical Engineering [ZK201803]

向作者/读者索取更多资源

The new nanoporous coordination polymer adsorbent NTU-66-Cu, prepared through cation exchanging, shows significantly improved C2H2/CO2 selectivity and enhanced C2H2 capacity, with excellent chemical stability for recycling C2H2/CO2 separation.
Safely and highly selective acetylene (C2H2) capture is a great challenge, because of its highly explosive nature, as well as its nearly similar molecule size and boiling point toward the main impurity of carbon dioxide (CO2). Adsorption separation has shown a promising future. Herein, a new nanoporous coordination polymer (PCP) adsorbent with fixed and free Cu ions (termed NTU-66-Cu) was prepared through post-synthetic approach via cation exchanging from the pristine NTU-66, an anionic framework with new 3, 4, 6-c topology and two kinds of cages. The NTU-66-Cu shows significantly improved C2H2/CO2 selectivity from 6 to 32 (v/v: 1/1) or 4 to 42 (v/v: 1/4) at low pressure under 298 K, along with enhanced C2H2 capacity (from 89.22 to 111.53 cm(3).g(-1)). More importantly, this observation was further validated by density functional theory (DFT) calculations and breakthrough experiments under continuous and dynamic conditions. Further, the excellent chemical stability enables this adsorbent to achieve recycle C2H2/CO2 separation without loss of C2H2 capacity.

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