Abstract

Lithium bis(pentafluoroethanesulfonyl)imide, Li[N(SO2C2F5)2], a typical fluorochemical aimed at better electrochemical performance of battery electrolytes, in superheated water was studied for its waste treatment. When Li[N(SO2C2F5)2] was reacted in pure superheated water at 300 °C, little F- ions were produced. In contrast, complete mineralization of the fluorine, sulfur, and nitrogen atoms in Li[N(SO2C2F5)2] was achieved when the reaction was performed in the presence of KMnO4. Specifically, when Li[N(SO2C2F5)2] was treated for 18 h with 158 mM of KMnO4, the F- and SO42- yields were 101 and 99%, respectively, and the sum of the NO3- and NO2- yields was 101%. In the gas phase, trace CO2 was detected and no CHF3, which has high global warming potential, was formed. Furthermore, the fluorine, sulfur, and nitrogen atoms in the analogues K[N(SO2C4F9)2] and K[N(SO2CF2)2CF2] also underwent complete mineralization using the same approach.

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