Screening of Deep Eutectic Solvents (DESs) as green CO2 sorbents: from solubility to viscosity
Deep eutectic solvents (DESs) as ionic liquid (IL) analogues show great potential for CO 2 capture. They exhibit favorable solvent properties and are considered to be economical alternatives to conventional ILs. In this study, we prepare 35 DESs and screen them in terms of their CO 2 solubility and...
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Veröffentlicht in: | New journal of chemistry 2017, Vol.41 (1), p.290 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Deep eutectic solvents (DESs) as ionic liquid (IL) analogues show great potential for CO 2 capture. They exhibit favorable solvent properties and are considered to be economical alternatives to conventional ILs. In this study, we prepare 35 DESs and screen them in terms of their CO 2 solubility and viscosity, both crucial factors to be considered when designing efficient CO 2 sorbents. The influence of salt and HBD type and structure, as well their molar ratio on the CO 2 solubility and viscosity of the DESs is investigated. The viscosity and CO 2 solubility of the DESs are compared with those of other DESs and conventional ILs. 15 DESs, which exhibit comparable CO 2 absorption capacity to choline chloride-urea DESs, glycerol DESs and fluorinated ILs, are chosen as the promising ones. The viscosities of the selected DESs are below 200 mPa s and are lower than those of choline chloride-based DESs. Since the viscosity of the DESs is relatively high, on a par with those of conventional ILs, the effect of water as a co-solvent is investigated in order to decrease the viscosity. The addition of water to the glycerol-based DESs improves the kinetics of absorption by decreasing the viscosity, thus increasing the CO 2 absorption capacity. Dry or aqueous DESs that demonstrate a high sorption capacity and low viscosity are chosen for additional analysis and characterization, and further functionalization will be carried out in the future to improve their sorption capacityy |
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ISSN: | 1369-9261 1144-0546 |
DOI: | 10.1039/c6nj03140d |