Reactions of [Me 3 PrN][(CF 3 SO 2 ) 2 N] and [C 3 mpip][(CF 3 SO 2 ) 2 N] (C 3 mpip = 1-methyl-1-propylpiperidium) in subcritical water were investigated to develop a technique for recycling fluorine element. By adding KMnO 4 to the system, quasi-complete mineralization of the ionic liquids was achieved at 300 °C. When [Me 3 PrN][(CF 3 SO 2 ) 2 N] was reacted for 18 h with 158 mM KMnO 4, F –, SO 4 2–, and NO 3 – yields were 98, 98, and 91%, respectively, and the amount of total organic carbon (TOC) was below the detection limit. [C 3 mpip][(CF 3 SO 2 ) 2 N] was also almost completely mineralized via the same treatment, affording F –, SO 4 2–, and NO 3 – 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 NO 2 – . 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 CHF 3 .
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Hori et al. (2020) studied this question.
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