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SO absorption in pure ionic liquids: Solubility and functionalization.

08:00 EDT 9th March 2020 | BioPortfolio

Summary of "SO absorption in pure ionic liquids: Solubility and functionalization."

The SO solubility in ionic liquids and absorption mechanisms with different functionalities, including ether, halide, carboxylate, dicarboxylate, thiocynate, phenol, amino, azole groups, etc., are presented in this review. Strategies of improving SO capture with low binding energy and the separation performance from CO are also concluded. Generally, moderate basicity is favourable for enhancing SO capacity and the water (below 6 wt%) effect on absorption is indefinite but generally slight. Introducing electron-withdrawing substituents such as nitrile, halogen, aldehyde and carboxylic groups are proposed to decrease the chemical absorption enthalpy between ionic liquid and SO in order to reduce regeneration power consumption. Although it is promising, the absorption enthalpy is still much higher than the physisorption performance especially of the ether-functionalized ones. The biocompatible choline-based, betaine-based, and amino acid ionic liquids have clear trends to be applied in SO capture due to their biodegradability, nontoxicity and easy accessibility. Generally, comparing to the traditional solvents, ionic liquids have made great improvement in SO capacity, however, the high viscosity and desorption energy are two main obstacles for SO absorption and separation. Molecular simulations have been applied to reveal the absorption regimes involving the roles of basic functionalities and physical interactions especially the hydrogen bonds, which could be referred for structure designing of the available ionic liquids with readily fluid characteristics and absorption ability.

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This article was published in the following journal.

Name: Journal of hazardous materials
ISSN: 1873-3336
Pages: 122504

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