Monoethanolamine (MEA) remains the predominant solvent for carbon dioxide (CO2) capture due to its rapid reaction kinetics, substantial absorption capacity, and demonstrated industrial effectiveness. Despite its established status, MEA-based systems are undergoing continuous development to lower energy requirements, enhance solvent stability, and expand operational adaptability. This review provides a critical assessment of recent progress in MEA-based CO2 capture, encompassing molecular-level understanding, advancements in reactor and process design, solvent modification strategies, and system-wide optimization. Recent theoretical and experimental research has improved the understanding of CO2 absorption mechanisms in MEA, highlighting the effects of reaction-product buildup, interfacial phenomena, and free amine availability on mass-transfer efficiency. Reboiler duty and comparable work have significantly decreased as a result of advances in process intensification, improved regeneration systems, and energy-integration techniques. New hybrid strategies that partially decouple capture from thermal regeneration, such as combined absorption–mineralization pathways, show promise for long-term CO2 sequestration. To address regeneration energy, corrosion, degradation, and cyclic stability, this review examines advances in MEA-based solvents, including aqueous blends, non-aqueous and biphasic systems, ionic liquids, and deep eutectic solvent hybrids. It also critically assesses the trade-offs of developments in intensified contactors, surfactants, nanomaterials, and catalysts. The growing role of digital optimization, machine learning, and computational modeling in MEA process design and control is highlighted. Overall, this analysis underscores MEA’s continued importance as a versatile platform for next-generation carbon capture, utilization, and storage.
Rahul R. Bhosale (Mon,) studied this question.