Reactions
of [Me3PrN][(CF3SO2)2N]
and [C3mpip][(CF3SO2)2N] (C3mpip = 1-methyl-1-propylpiperidium) in subcritical
water were investigated to develop a technique for recycling fluorine
element. By adding KMnO4 to the system, quasi-complete
mineralization of the ionic liquids was achieved at 300 °C. When
[Me3PrN][(CF3SO2)2N] was
reacted for 18 h with 158 mM KMnO4, F–, SO4
2–, and NO3
– yields were 98, 98, and 91%, respectively, and the amount of total
organic carbon (TOC) was below the detection limit. [C3mpip][(CF3SO2)2N] was also almost
completely mineralized via the same treatment, affording F–, SO4
2–, and NO3
– yields of 94, 97, and 96%, respectively, with no detectable TOC.
The rest of the nitrogen atoms were well accounted for by the formation
of NO2
–. Compared with a previous reported
method using FeO, our approach reduces the reaction temperature for
complete mineralization by 76 °C and suppresses the formation
of environmentally undesirable CHF3.