2013
DOI: 10.1039/c3ee41016a
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Improving the regeneration of CO2-binding organic liquids with a polarity change

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Cited by 82 publications
(153 citation statements)
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References 30 publications
(39 reference statements)
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“…The main advantages of using all-organic solvents are their lower cost of energy due to the elimination of the vaporization of water, lower stripper reboiler temperature, and their tunable physicochemical properties. Therefore, they have considerable potential to be an efficient CO 2 capture solvent due to high CO 2 binding capacities, low heat capacities, less solvent loss during CO 2 stripping and lower energy requirement for regeneration than the traditional aqueous amine systems [19]. Consequently, there Fig.…”
Section: Co 2 Binding Organic Liquids (Co 2 Bols)mentioning
confidence: 99%
“…The main advantages of using all-organic solvents are their lower cost of energy due to the elimination of the vaporization of water, lower stripper reboiler temperature, and their tunable physicochemical properties. Therefore, they have considerable potential to be an efficient CO 2 capture solvent due to high CO 2 binding capacities, low heat capacities, less solvent loss during CO 2 stripping and lower energy requirement for regeneration than the traditional aqueous amine systems [19]. Consequently, there Fig.…”
Section: Co 2 Binding Organic Liquids (Co 2 Bols)mentioning
confidence: 99%
“…They have tunable physicochemical properties; the solvent reverts back to its less-polar non-ionic form and is ready for future CO 2 uptake (Tao Yu et al 2008). The main advantages of these systems are high CO 2 binding capacities, low heat capacities and lower energy requirement for regeneration as compared to aqueous alkanolamine solutions (Mathias et al 2013). Wang et al developed several strategies to reduce volatility of superbase-derived absorbents by making them such as alcohol-functionalized ionic liquids (Wang et al 2010).…”
Section: Introductionmentioning
confidence: 97%
“…It is presumed that the base of CO 2 BOL does not react directly with CO 2 , as amines react to form carbamates. Conversely, the alcohol group in the CO 2 BOL reacts firstly with CO 2 to form an alkyl carbonic acid, and then protonates the base to form a liquid alkylcarbonate (Mathias et al 2013). Alkyl carbonate salts formed are non-volatile ionic compounds and they do not contain as much hydrogen bond as carbamate and bicarbonate salts do.…”
Section: Introductionmentioning
confidence: 98%
“…13 Also, non-ionic (low polarity) regions may provide voids with high CO2 solubility and unreacted solvent available to complex with CO2, accounting for the higher than expected CO2 mass transfer in and out of SWILs. 32 This may explain how a non-polar additive dissolves into solution to change the solvation free energies of the ions in solution, facilitating CO2 release. 32 Alternatively, concentrated ionic regions could provide favourable solvation environments for catalysts for CO2 hydrogenations 6 or precursors for nanoparticle synthesis.…”
mentioning
confidence: 99%
“…32 This may explain how a non-polar additive dissolves into solution to change the solvation free energies of the ions in solution, facilitating CO2 release. 32 Alternatively, concentrated ionic regions could provide favourable solvation environments for catalysts for CO2 hydrogenations 6 or precursors for nanoparticle synthesis. 8,9,12 .…”
mentioning
confidence: 99%