Abstract
Direct nitrolysis of 3,7-dinitro-1,3,5,7-tetraazabicyclo[3,3,1]nonane (DPT) is a feasible way to synthesize HMX, and it has multiple practical applications. In this paper, a new nitrolysis process involving the use of an N2O5-HNO3 system catalyzed by acidic ionic liquids (AILs) was developed. The results show that [Et3NH]TsO was the best catalyst among the 28 AILs used and that HMX was formed at a higher yield of 61%, compared to 45% without any AIL. Moreover, with the addition of N2O5, the yield was further increased to a maximum value of 69%. The AILs were also efficiently recovered by simple extractions without any apparent loss of catalytic activity, even after five runs.
Original language | English |
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Pages (from-to) | 2677-2682 |
Number of pages | 6 |
Journal | Bulletin of the Korean Chemical Society |
Volume | 32 |
Issue number | 8 |
DOIs | |
State | Published - 20 Aug 2011 |
Externally published | Yes |
Keywords
- Acidic ionic liquid
- DPT
- HMX
- N2O5
- Nitrolysis