Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Static high pressure study of nitric oxide chemistry: proposed mechanism for nitric oxide detonation. [Shock initiated detonation]

Conference ·
OSTI ID:5711749
The chemistry of nitric oxide under static high pressure conditions has been studied using diamond anvil cells and spectroscopic methods. Pressurized samples warmed rapidly to room temperature undergo facile disproportionation to form N/sub 2/O, N/sub 2/O/sub 3/, N/sub 2/O/sub 4/, and NO/sup +/NO/sub 3//sup -/. Nitric oxide maintained at 80 K is observed to react at ca. 2.5 GPa to form, dominantly, N/sub 2/, O/sub 2/, and NO/sup +/NO/sub 3//sup -/. The complex chemistry of nitric oxide is best explained in terms of two competing primary reaction mechanisms involving the direct formation of N/sub 2/ and O/sub 2/, and disproportionation to form N/sub 2/O and NO/sup +/NO/sub 3//sup -/. The disproportionation reaction, which is favored under higher temperature conditions, releases two-thirds of the total energy content, and is believed to be important in the early chemistry accompanying shock-initiation of nitric oxide. Laboratory scale detonation studies, where the gaseous products are analyzed spectroscopically, show evidence for, dominantly, disproportionation and a small amount of N/sub 2//O/sub 2/ production. This study points to the importance of condensed phase concerted reactions as well as ions and ionic reaction mechanisms in the shock initiated detonation of HE's. 14 refs., 3 figs., 1 tab.
Research Organization:
Los Alamos National Lab., NM (USA)
DOE Contract Number:
W-7405-ENG-36
OSTI ID:
5711749
Report Number(s):
LA-UR-85-1176; CONF-850706-16; ON: DE85010795
Country of Publication:
United States
Language:
English