4.7 Article

Dual-functionalized ionic liquid biphasic solvents with aqueous-lean for industrial carbon capture: Energy-saving and high efficiency

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 315, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2023.123722

Keywords

Biphasic solvents; Ionic liquids; Poly (ethylene glycol) dimethyl ether; CO2 capture; Energy efficiency

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A new sustainable dual-functionalized amino ionic liquid biphasic solvent was proposed for CO2 capture. The solvent exhibited a CO2 absorption loading of 1.95 mol CO2 center dot L-1 solvent and a CO2-rich phase with a loading of 4.65 mol CO2 center dot L-1 solvent. The solvent could be regenerated by 92.3% in 10 minutes at 373 K, and its regeneration efficiency remained at 83% after 10 cycles. The energy consumption for CO2 desorption was significantly reduced compared to ethanolamine. This solvent provides a sustainable strategy for advancing carbon capture technologies.
A novel, sustainable, dual-functionalized amino ionic liquid biphasic solvent of 3-(Dimethylamino)-1-propyl-amine-1,2,4-triazole/poly (ethylene glycol) dimethyl ether/water ([DMAPA][TZ]/NHD/water) was proposed for CO2 capture to reduce the consumption of regeneration energy. Experimental results showed that the CO2 ab-sorption loading of the solvent was 1.95 mol CO2 center dot L-1 solvent at a CO2 partial pressure of 15 kPa. The volume of the CO2-rich phase was 40 vol% of the total volume, with a loading of up to 4.65 mol CO2 center dot L-1 solvent, ac-counting for approximately 95.4% of the blended CO2 loading in the solvent. The CO2-rich phase could be re-generated by 92.3% in 10 min at 373 K, without the presence of a lean phase. The regeneration efficiency of the solvent was maintained at 83% after 10 adsorption and desorption cycles. The reaction, regeneration, and phase -change mechanism were investigated using 13C NMR and phase composition analysis. CO2 reacted with [DMAPA][TZ] to form two kinds of carbamate during solubilization, and all carbamates could be further hy-drolyzed to form HCO3-and CO32-. The solvent effect, phase-change behavior, and CO2 physical dissolution of NHD could promote the absorption and desorption rate and absorption capacity of CO2. The energy consumption for CO2 desorption could be reduced to 1.335 GJ center dot t-1 CO2, which was 67% lower than that of 30 wt% etha-nolamine (3.99 GJ center dot t-1 CO2), given the lower heat of reaction, specific heat capacity, and solvent loss. Thus, this solvent presents a sustainable strategy for advancing carbon capture technologies.

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