4.8 Article

Rational Tuning of Ultramicropore Dimensions in MOF-74 for Size-Selective Separation of Light Hydrocarbons

期刊

CHEMISTRY OF MATERIALS
卷 33, 期 19, 页码 7686-7692

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.1c01657

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资金

  1. Basic Science Research Program through the National Research Foundation of Korea - Ministry of Science, ICT, & Future Planning [2017R1A2B4004029]
  2. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [NRF-2018R1C1B6002461]
  3. National Research Foundation of Korea [2017R1A2B4004029] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The rational augmentation of metal-organic framework Mg-MOF-74 offers a promising alternative for the energy-intensive separation of light hydrocarbon mixtures. The newly synthesized tpt-Mg-MOF-74 shows a high diffusive selectivity for separating ethane/propane, demonstrating the potential for enhanced efficiency in separation applications without sacrificing pore volume.
The separation of light hydrocarbon mixtures is one of the most important yet energy-intensive processes in the petrochemical industry. Solid adsorbent materials could potentially not only lower energy costs but also offer higher efficiency as an alternative means to traditionally energy-intensive separation methods such as distillation, absorption, and extraction. Here, rational augmentation of the metal-organic framework, Mg-MOF-74, was designed in silico to enhance kinetic selectivity of the material, while imposing a minimal reduction in the adsorption working capacities for light hydrocarbons. From the computer-aided design, we synthesized 2,4,6-tri(4pyridyl)-1,3,5-triazine-inserted Mg-MOF-74 (tpt-Mg-MOF-74) and successfully characterized the structure. This material can kinetically separate ethane/propane with an unprecedented diffusive selectivity of similar to 49 owing to its distinctive pore size and provides evidence that metal-organic framework need not sacrifice pore volume for enhanced kinetic selectivity in separation applications.

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