Abstract
∈-HNIW was prepared by a one-pot method in concentrated nitric acid from tetraacetyldiformylhexaazaisowurtzitane (TADFIW), γ-HNIW was firstly obtained, then γ-HNIW was directly transformed to ∈-HNIW in the solution in which nitration reaction occurred. The acid number of ∈-HNIW prepared by the method mentioned above is less than 0.2%o, yield of ∈-HNIW is up to 91%, and the purity of ∈-HNIW is up to 99.5%. Because steps of filtration and drying of γ-HNIW were omitted, the process by which ∈-HNIW was prepared simplified greatly.
Original language | English |
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Pages (from-to) | 468-471 |
Number of pages | 4 |
Journal | Propellants, Explosives, Pyrotechnics |
Volume | 32 |
Issue number | 6 |
DOIs | |
Publication status | Published - Dec 2007 |
Keywords
- Crystal transformation
- Hexanitrohexaazaisowurtzitane (HNIW)
- Hydrolysis-nitration
- One-pot method
- Tetraacetyldiformylhexaazaisowurtzitane (TADFIW)