Final published version
Licence: CC BY: Creative Commons Attribution 4.0 International License
Research output: Contribution to Journal/Magazine › Journal article › peer-review
Article number | e2362 |
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<mark>Journal publication date</mark> | 2/07/2025 |
<mark>Journal</mark> | Greenhouse Gases: Science and Technology |
Publication Status | E-pub ahead of print |
Early online date | 2/07/25 |
<mark>Original language</mark> | English |
This study investigates the screening of lithium-based salts in non-aqueous electrolyte solutions of monoethanolamine (MEA) for potential use in integrated carbon capture and conversion (ICCC) technology. Experimental measurements of density, viscosity, nitrous oxide (N 2O) solubility, and CO 2 solubility were conducted for various lithium salts, including lithium chloride (LiCl), lithium bromide (LiBr), and lithium nitrate (LiNO 3), in MEA–dimethyl sulfoxide (DMSO) system at 303.15 K at different CO 2 pressures ranging from 344 to 1379 kPa. The results indicated that the addition of lithium salts to the amine solution significantly enhances CO 2 absorption capacity, exceeding the benchmark value of 0.5 mol CO 2/mol MEA typically reported for 5 M MEA aqueous systems. The highest CO 2 solubility in the system was observed following the order 2 M MEA + 0.5 M LiBr < 2 M MEA + 0.5 M LiNO 3 < 2 M MEA + 0.5 M LiCl in DMSO with corresponding values of 1.2213, 1.2801, and 1.3381 mol CO 2/mol MEA, respectively, identifying LiCl as the most effective additive. It was also found that using DMSO as an organic solvent greatly enhanced the CO 2 absorption capacity compared to water, evidenced by Henry's law constant determined using N 2O analogy, in addition to its lower sensible heat than water. The findings demonstrate that MEA in organic solvent shows a promising performance in CO 2 capture, with CO 2 loading higher than the industrial standard (<0.5 mol CO 2/mol MEA). Ultimately, the screening process outlined in this study serves as a foundation for future research aimed at optimizing electrolyte formulations for enhanced carbon capture efficiency.