4.6 Article

Efficient ethylene/ethane separation through ionic liquid-confined covalent organic framework membranes

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 10, 期 10, 页码 5420-5429

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta10516g

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资金

  1. National Natural Science Foundation of China [21838008, U20B2023, 21621004, 21490583, 21878215]
  2. National Key R & D Program of China [2017YFB0603400]
  3. Program of Introducing Talents of Discipline to Universities [BP0618007]

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This study demonstrates the application of covalent organic framework (COF) membranes for efficient ethylene/ethane separation. By loading and modifying the membranes with a silver ion-containing ionic liquid layer, the membrane channel size is reduced and high ethylene/ethane selectivity and ethylene permeance are achieved. The COF membranes also exhibit superior chemical stability and long-term operation stability.
Organic framework materials, owing to the long-range ordered channels, uniform channel sizes and readily tailored functionalities, are expected to become next generation membrane materials for molecular separations. In this study, for the first time, we demonstrate the utilization of covalent organic framework (COF) membranes for efficient ethylene/ethane separation. The COF membranes are loaded and modified with a silver ion-containing ionic liquid layer. Owing to the distinct confinement effects, the membrane channel size is first reduced by the physically absorbed ionic liquid and further reduced by the chemically bound ethylene molecules. When the membrane channel size is tuned to 0.87 nm, which is still larger than both ethylene (0.42 nm) and ethane (0.44 nm) molecules, an extraordinarily high ethylene/ethane selectivity up to 120 and ethylene permeance of 135 GPU are achieved simultaneously, which surpass most of the state-of-the-art membranes towards ethylene/ethane separation. Our strategy was also validated by propylene/propane separation. Moreover, the COF membranes exhibit superior chemical stability and long-term operation stability. Strikingly, our strategy opens a novel path for enabling membranes with larger pore/channel sizes for separating smaller molecule mixtures.

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