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Journal of materials chemistry. A, Materials for energy and sustainability, 2021-11, Vol.9 (43), p.24495-2452
2021
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Details

Autor(en) / Beteiligte
Titel
A highly stable MOF with F and N accessible sites for efficient capture and separation of acetylene from ternary mixtures
Ist Teil von
  • Journal of materials chemistry. A, Materials for energy and sustainability, 2021-11, Vol.9 (43), p.24495-2452
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2021
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Considering the important applications and purification requirement of C 2 hydrocarbons in the industry, the separation of C 2 in mixtures is a vital task. To achieve this goal, herein a new Ni 2+ -based metal-organic framework (MOF) has been solvothermally prepared by utilizing a tetrazolyl-carboxyl ligand and 4,4′-bipyridine coligands as well as incorporating F − ions. The MOF shows a unique pillared-layer framework based on the novel metal-tetrazolate-carboxylate-fluorine chains, and possesses high chemical stability. Owing to the exposed adsorption sites of uncoordinated N atoms and F − ions in the channels, the MOF had high loadings for C 2 H 2 and selectivity for C 2 H 2 over C 2 H 4 , C 2 H 6 , CO 2 and CH 4 . Under ambient conditions, dynamic breakthrough experiments revealed that the MOF performs effective separation of C 2 H 2 from binary (C 2 H 2 -CH 4 , C 2 H 2 -C 2 H 6 , C 2 H 2 -C 2 H 4 , and C 2 H 2 -CO 2 ) and ternary (C 2 H 2 -CO 2 -CH 4 , C 2 H 2 -C 2 H 6 -CH 4 , C 2 H 2 -C 2 H 4 -CH 4 , and C 2 H 2 -C 2 H 4 -C 2 H 6 ) mixtures. The comparison based on the GCMC calculation revealed the crucial role of the accessible N and F sites for the selective capture of C 2 H 2 . A stable Ni-MOF with high adsorption selectivity for C 2 H 2 was constructed by the strategy of incorporating active N and F sites in the porous surface, showing the dynamic separation of C 2 H 2 from binary and ternary mixtures in one-step.
Sprache
Englisch
Identifikatoren
ISSN: 2050-7488
eISSN: 2050-7496
DOI: 10.1039/d1ta05720k
Titel-ID: cdi_rsc_primary_d1ta05720k

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