Fenton oxidation of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX)

Oxidation of the high explosives hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) using Fentonʹs reagent proceeds rapidly between 20°C and 50°C at pH 3. At an H2O2 : Fe2+ : RDX molar ratio of 5178 : 48 : 1, RDX and HMX were completely removed in 1 to 2 h. All the experimental data could be fit to a pseudo first-order rate equation. The reaction rate was also strongly dependent on Fenton’s reagent concentrations. NO3− and N2 were identified as nitrogen byproducts from RDX and HMX oxidation. The experiment with radiolabeled RDX showed that approximately 37% of organic carbon in RDX was mineralized to CO2. We observed formaldehyde and formic acid as a short-lived intermediate. No other volatile or nonvolatile byproducts were found from GC/MS analysis. The results show that RDX and HMX can be effectively mineralized with Fentonʹs reagents.