4.6 Article

Metal Microporous Aromatic Polymers with Improved Performance for Small Gas Storage

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 21, 期 38, 页码 13357-13363

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201501594

关键词

doping; ferrocene; gas adsorption and delivery; microporous materials; polymers

资金

  1. National Science Foundation of China [21204103, 21376272]
  2. China Postdoctoral Science Foundation [2012M521535]
  3. China Postdoctoral Science Foundation Specialized Funded project [2014T70787]
  4. State Key Laboratory of Fine Chemicals [KF1206]
  5. State Key Laboratory of Advanced Technology for Materials and Processing [2015-KF-8]
  6. Fundamental Research Funds for the Central Universities of Central South University [2014zzts155]
  7. National Science Foundation of China [21204103, 21376272]
  8. China Postdoctoral Science Foundation [2012M521535]
  9. China Postdoctoral Science Foundation Specialized Funded project [2014T70787]
  10. State Key Laboratory of Fine Chemicals [KF1206]
  11. State Key Laboratory of Advanced Technology for Materials and Processing [2015-KF-8]
  12. Fundamental Research Funds for the Central Universities of Central South University [2014zzts155]

向作者/读者索取更多资源

A novel metal-doping strategy was developed for the construction of iron-decorated microporous aromatic polymers with high small-gas-uptake capacities. Cost-effective ferrocene-functionalized microporous aromatic polymers (FMAPs) were constructed by a one-step Friedel-Crafts reaction of ferrocene and s-triazine monomers. The introduction of ferrocene endows the microporous polymers with a regular and homogenous dispersion of iron, which avoids the slow reunion that is usually encountered in previously reported metal-doping procedures, permitting a strong interaction between the porous solid and guest gases. Compared to ferrocene-free analogues, FMAP-1, which has a moderate BET surface area, shows good gas-adsorption capabilities for H-2 (1.75wt% at 77K/1.0bar), CH4 (5.5wt% at 298K/25.0bar), and CO2 (16.9wt% at 273K/1.0bar), as well as a remarkably high ideal adsorbed solution theory CO2/N-2 selectivity (107v/v at 273K/(0-1.0)bar), and high isosteric heats of adsorption of H-2 (16.9kJmol(-1)) and CO2 (41.6kJmol(-1)).

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