Molecular engineering of low-viscosity deep eutectic solvents for high-capacity and selective SO₂ capture.
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| Title: | Molecular engineering of low-viscosity deep eutectic solvents for high-capacity and selective SO₂ capture. |
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| Authors: | Cheng, Li-Ming1 (AUTHOR), Yin, Kang-Shou1 (AUTHOR), Xu, Jin-Bo1 (AUTHOR), Liu, Yong-Hui1 (AUTHOR), Wang, Shao-He1 (AUTHOR), Du, Jun1 (AUTHOR) dujun@ncu.edu.cn |
| Source: | Colloids & Surfaces A: Physicochemical & Engineering Aspects. May2026:Part 2, Vol. 737, pN.PAG-N.PAG. 1p. |
| Subjects: | Sulfur dioxide, Viscosity, Absorption, Environmental protection, Solvents, Hydrogen bonding, Chemical engineering, Imidazoles |
| Abstract: | Sulfur dioxide (SO₂) is a toxic industrial pollutant and valuable chemical feedstock, making its efficient capture critical for environmental protection and resource recycling. This work rationally designed a novel DES system using 1,3-dimethylimidazolium chloride ([Dim]Cl) as the hydrogen-bond acceptor (HBA) and imidazole as the hydrogen-bond donor (HBD), leveraging a previously underexplored design principle: structural simplification of the HBA cation to mitigate viscosity without sacrificing absorption performance. The optimized [Dim]Cl+imidazole (1:0.5) DES achieves an exceptional SO₂ absorption capacity of 20.69 ± 0.73 mol/kg at 298.2 K and 102.2 kPa (exceeds the majority) while maintaining a low viscosity of 47.1 ± 3.3 cP—over 4-fold lower than analogous [Emim]Cl-based DESs (198.3 cP) with comparable capacity and far below the viscosity of most high-capacity ILs (>200 cP). This low viscosity promotes rapid mass transfer, as confirmed by pseudo-first-order kinetics (k₁=0.089 ± 0.016 mol/(kg·min), R²> 0.98). The DES also exhibits outstanding selectivity (SO₂/CO₂=547, SO₂/N₂=1169) and perfect regenerability over ten cycles. At low concentrations(<10kpa), the DES exhibits enhanced selectivity(SO₂/CO₂=5013, SO₂/N₂=15563). A synergistic absorption mechanism was elucidated via spectroscopic analysis and quantum chemical calculations: SO₂ is simultaneously captured by multiple sites—Cl⁻ (strong nucleophilic coordination) and the imidazole ring (weak basicity and hydrogen-bonding facilitation). This multi-site interaction is the origin of the DES's superior performance. [Display omitted] [ABSTRACT FROM AUTHOR] |
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| Database: | Engineering Source |
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