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Supported deep eutectic liquid membranes with highly selective interaction sites for efficient CO2 separation
Saeed, U ; Sharif University of Technology | 2021
497
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- Type of Document: Article
- DOI: 10.1016/j.molliq.2021.117509
- Publisher: Elsevier B.V , 2021
- Abstract:
- This study demonstrates a new strategy in which deep eutectic solvents (DES), a new class of sustainable organic solvents, were impregnated into micro porous polymer support for separation of CO2 from CH4. Three different types of DESs were prepared by mixing and subsequent heating of betaine as hydrogen bond acceptor (HBA) in combination with either glycerol (G), ethylene glycol (EG) or urea (U) as hydrogen bond donors (HBD) in 1:3 stoichiometric mole ratio. The Fourier transform infrared (FTIR) spectroscopy was performed to confirm the formation of DESs. The gas permeation results showed that permeability of CO2 increased from 31.23 to 35.67 Barrer on substitution of HBD from glycerol to urea. The selectivity of CO2/CH4 increased from 43.32 to 57.53 for the substitution of HBD from ethylene glycol to urea. These intriguing results are ascribed by the high interaction of CO2 with DES in which solubility of CO2 is directly influenced by the HBDs. The membranes were also tested under conditions relevant to industrial feed gas and the results were compared with the competing state of the art membranes. The impregnation of DESs into the porous polymer supports provides a pathway for future material design for the efficient separation of CO2 from gases mixtures. © 2021 Elsevier B.V
- Keywords:
- Carbon dioxide ; Ethylene ; Ethylene glycol ; Eutectics ; Fourier transform infrared spectroscopy ; Gas permeable membranes ; Glycerol ; Hydrogen bonds ; Metabolism ; Organic solvents ; Polyols ; Separation ; Betaine-ethylene glycol ; Betaine-glycol ; Betaine-urea ; CH 4 ; CO2 separation ; Deep eutectic solvents ; Eutectic liquid ; Hydrogen bond donors ; Polymer supports ; Porous polymers ; Urea
- Source: Journal of Molecular Liquids ; Volume 342 , 2021 ; 01677322 (ISSN)
- URL: https://www.sciencedirect.com/science/article/abs/pii/S0167732221022339