A new
series of functionalized ionic liquids (ILs) with 1,1,3,3-tetramethylguanidine
([TMG]+) cations as well as dicarboxylic acid anions {[−OOC–(CH2–CH2)
n
–COO–], where n = 1, 3, and 5} was synthesized, and their
SO2 absorption properties were investigated. A high SO2 absorption capacity of the prepared ILs was achieved. The
molar ratios of SO2 to [TMG][succinic acid] {([TMG][SUC])
(n = 1)}, [TMG][suberic acid] {([TMG][SUB]) (n = 3)}, and [TMG][dodecanedioic acid] {([TMG][DOD]) (n = 5)} were 4.76, 5.96, and 5.96, respectively. The evidence
of spectroscopic measurements and quantum chemical calculations confirmed
that SO2 could interact with the carboxyl and adjacent
methylene groups on the anion as well as the amino group on the cation.
The SO2 absorption capacity of these ILs was strongly influenced
by their asymmetry and space resistance. The high symmetry and large
steric hindrance could reduce the SO2 absorption capacity
of ILs.
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