Effect of environment on iodine oxidation state and reactivity with aluminum
Iodine oxide is a highly reactive solid oxidizer and with its abundant generation of iodine gas during reaction, this oxidizer also shows great potential as a biocidal agent. A problem with using I 2 O 5 in an energetic mixture is its highly variable reactive behavior. This study isolates the variab...
Gespeichert in:
Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2016-04, Vol.18 (16), p.11243-1125 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Iodine oxide is a highly reactive solid oxidizer and with its abundant generation of iodine gas during reaction, this oxidizer also shows great potential as a biocidal agent. A problem with using I
2
O
5
in an energetic mixture is its highly variable reactive behavior. This study isolates the variable reactivity associated with I
2
O
5
as a function of its chemical reaction in various environments. Specifically, aluminum fuel and iodine oxide powder are combined using a carrier fluid to aid intermixing. The carrier fluid is shown to significantly affect the oxidation state of iodine oxide, thereby affecting the reactivity of the mixture. Four carrier fluids were investigated ranging in polarity and water miscibility in increasing order from hexane < acetone < isopropanol < water as well as untreated, dry-mixed reactants. Oxidation state and reactivity were examined with experimental techniques including X-ray photoelectric spectroscopy (XPS) and differential scanning calorimetry (DSC). Results are compared with thermal equilibrium simulations. Flame speeds increased with polarity of the fluid used to intermix the powder and ranged from 180 to 1202 m s
−1
. The I
2
O
5
processed in the polar fluids formed hydrated states of iodine oxide: HIO
3
and HI
3
O
8
; and, the nonpolar and dry-mixed samples formed: I
2
O
4
and I
4
O
9
. During combustion, the hydrated iodine oxides rapidly dehydrated from HIO
3
to HI
3
O
8
and from HI
3
O
8
to I
2
O
5
. Both steps release 25% of their mass as vapor during combustion. Increased gas generation enhances convective energy transport and accounts for the increase in reactivity seen in the mixtures processed in polar fluids. These results explain the chemical mechanisms underlying the variable reactivity of I
2
O
5
that are a function of the oxide's highly reactive nature with its surrounding environment. These results will significantly impact the selection of carrier fluid in the synthesis approach for iodine containing reactive mixtures.
Iodine oxide is a highly reactive solid oxidizer and with its abundant generation of iodine gas during reaction, this oxidizer also shows great potential as a biocidal agent. |
---|---|
ISSN: | 1463-9076 1463-9084 |
DOI: | 10.1039/c5cp06998j |