Abstract
Efficient and reversible absorption of SO2 by deep eutectic solvents (DESs) has drawn much attention in recent years. In this work, a new type of deep eutectic solvents (DESs) were synthesized via pyridine derivatives, nicotinamide, aminopyridines and hydroxypyridines, as the hydrogen bond donors (HBDs) with common quaternary ammonium salt ionic liquids (ILs) as hydrogen bond acceptors (HBAs). The studied DESs exhibited an attractive absorption behavior for SO2, especially for low concentration SO2. The 1-allyl-3-methylimidazolium chloride (AmimCl)/2-aminopyridine (2-NH2Py) (2:1) and 1-butyl-3-methylimidazolium chloride (BmimCl)/3-aminopyridine (3-NH2Py) (2:1) could capture 0.273 and 0.223 g SO2/g DES at 293 K and 1.0 kPa, respectively, surpassing that of most DESs and ILs in the present literature. The influence of DES composition, temperature and pressure on SO2 absorption performance was systematically investigated. Moreover, the absorption mechanism studied by nuclear magnetic resonance (NMR) and Fourier transform infrared (FT-IR) spectroscopies indicated that the efficient absorption of SO2 was ascribed to the chemical interaction between the pyridine nitrogen atom and SO2.
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