Amino acid–based deep eutectic solvent functionalized NH2-UiO-66 for selective CO2 capture from flue gas

Efficient CO<sub>2</sub> capture from flue gas is a critical step toward mitigating greenhouse gas emissions and enabling its subsequent utilization. The relatively low CO<sub>2</sub> partial pressure in flue gas necessitates the development of highly selective adsorbents capable of producing pure CO<sub>2</sub> in a single step with minimal energy input. In this study, an amino acid-based deep eutectic solvent (DES) was immobilized onto NH<sub>2</sub>-UiO-66 using impregnation to enhance CO<sub>2</sub> capture performance. Herein, proline (Pro) and glycine (Gly), two amino acids, were used as HBAs and monoethanolamine (MEA) was employed as an HBD. The DES provides high CO<sub>2</sub> solubility through amine-CO<sub>2</sub> interactions, while the MOF framework serves as a microporous reservoir for gas storage. Structural and physicochemical analyses, including Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (FESEM) with Energy-Dispersive X-ray Spectroscopy (EDX), Thermogravimetric Analysis (TGA), and Brunauer-Emmett-Teller (BET) surface area analysis confirmed successful DES loading without compromising the intrinsic microporosity of NH<sub>2</sub>-UiO-66. CO<sub>2</sub> adsorption was evaluated using a quartz crystal microbalance (QCM) at pressures up to 1 bar and 288.15-308.15 K. The adsorption isotherms were well-described by a hybrid Redlich-Peterson model, indicating a predominant chemisorption mechanism. DES functionalization increased the CO<sub>2</sub> adsorption capacity of the MOF by factors of 1.54 (DES1@MOF) and 0.75 (DES2@MOF) despite a reduction in pore volume, due to enhanced adsorbate-DES interactions. The composites exhibited improved CO<sub>2</sub>/N<sub>2</sub> selectivity, favorable adsorption thermodynamics, and maintained over 98% of their initial capacity after 10 adsorption/desorption cycles. These results highlight amino acid-based DES@MOF composites as promising candidates for energy-efficient CO<sub>2</sub> capture and utilization from flue gas.

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Journal
Scientific Reports
Published
2025-11-26
DOI
https://doi.org/10.1038/s41598-025-29617-8
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
0.00

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article

Amino acid–based deep eutectic solvent functionalized NH2-UiO-66 for selective CO2 capture from flue gas

Abbas Mehrdad, Narmin Noorani
Scientific Reports
Carbon Dioxide Capture Technologies
article

Amino acid–based deep eutectic solvent functionalized NH2-UiO-66 for selective CO2 capture from flue gas

Abbas Mehrdad, Narmin Noorani
article en

Abstract

Efficient CO<sub>2</sub> capture from flue gas is a critical step toward mitigating greenhouse gas emissions and enabling its subsequent utilization. The relatively low CO<sub>2</sub> partial pressure in flue gas necessitates the development of highly selective adsorbents capable of producing pure CO<sub>2</sub> in a single step with minimal energy input. In this study, an amino acid-based deep eutectic solvent (DES) was immobilized onto NH<sub>2</sub>-UiO-66 using impregnation to enhance CO<sub>2</sub> capture performance. Herein, proline (Pro) and glycine (Gly), two amino acids, were used as HBAs and monoethanolamine (MEA) was employed as an HBD. The DES provides high CO<sub>2</sub> solubility through amine-CO<sub>2</sub> interactions, while the MOF framework serves as a microporous reservoir for gas storage. Structural and physicochemical analyses, including Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (FESEM) with Energy-Dispersive X-ray Spectroscopy (EDX), Thermogravimetric Analysis (TGA), and Brunauer-Emmett-Teller (BET) surface area analysis confirmed successful DES loading without compromising the intrinsic microporosity of NH<sub>2</sub>-UiO-66. CO<sub>2</sub> adsorption was evaluated using a quartz crystal microbalance (QCM) at pressures up to 1 bar and 288.15-308.15 K. The adsorption isotherms were well-described by a hybrid Redlich-Peterson model, indicating a predominant chemisorption mechanism. DES functionalization increased the CO<sub>2</sub> adsorption capacity of the MOF by factors of 1.54 (DES1@MOF) and 0.75 (DES2@MOF) despite a reduction in pore volume, due to enhanced adsorbate-DES interactions. The composites exhibited improved CO<sub>2</sub>/N<sub>2</sub> selectivity, favorable adsorption thermodynamics, and maintained over 98% of their initial capacity after 10 adsorption/desorption cycles. These results highlight amino acid-based DES@MOF composites as promising candidates for energy-efficient CO<sub>2</sub> capture and utilization from flue gas.

Scientific ReportsVol. 15(1)
University of Tabriz (IR)
University of Tabriz
Openalex Percentile: Top 62%
Carbon Dioxide Capture Technologies
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