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Experimental measurements and modelling of the CO2 solubility in L-lysine co-promoted CESAR-1 (Bio-CESAR) solutions

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Abstract

Carbon capture technologies are vital for mitigating carbon dioxide (CO2) emissions in bioenergy and energy-from-waste power plants. Among them, solvent-based absorption is the most widely used in above industries. Mono-ethanolamine (MEA) is the pre-dominant and an established solvent for absorption based-carbon capture. However, newer solvent blends, like mixtures of MEA and N-methyl diethanolamine (MDEA), and CESAR-1 (a blend of 2-amino-2-methyl-1-propanol and piperazine) are being considered for future plants as they offer 10–15% enhanced performance and ∼20% improved capacity. This study presents the first results of adding L-lysine as a co-promoter for CESAR-1, to improve its CO2 capture efficiency and capacity. The proposed blend, Bio-CESAR (a blend of 2-amino-2-methyl-1-propanol, piperazine, and L-lysine), was experimentally tested for CO2 solubility across a range of pressures (30–500 kPa, CO2 partial pressure range of 3–50 kPa) and temperatures (298.15–343.15 K), and its performance was compared to conventional CESAR-1 and MEA solutions. Results show that Bio-CESAR offers 15% higher CO2 loading and equilibrium CO2 solubility at average compared to CESAR-1, suggesting potential for improved cyclic efficiency in industrial applications. The enhanced CO2 absorption performance of Bio-CESAR is attributed to the incorporation of L-lysine, which modifies CO2–solvent interactions and solution speciation within the CESAR-1 framework. Results from this macroscopic study suggest that the bio-derived amino acid act synergistically with the conventional amine components, leading to improved equilibrium CO2 loading. This study provides a fundamental insight for the use of L-lysine (and not its alkaline salt) in enhancing solvent performance and reducing environmental risks in carbon capture systems.
Original languageEnglish
Article number139618
Number of pages7
JournalFuel
Volume426
Early online date26 Apr 2026
DOIs
Publication statusE-pub ahead of print - 26 Apr 2026

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