16 research outputs found
Polysaccharide-Thickened Aqueous Fluoride Solutions for Rapid Destruction of the Nerve Agent VX. Introducing the Opportunity for Extensive Decontamination Scenarios
Among the chemical warfare agents,
the extremely toxic nerve agent
VX (<i>O</i>-ethyl <i>S</i>-2-(diisopropylamino)Âethyl
methylphosphonothioate) is a target of high importance in the development
of decontamination methods, due to its indefinite persistence on common
environmental surfaces. Liquid decontaminants are mostly characterized
by high corrosivity, usually offer poor coverage, and tend to flow
and accumulate in low areas. Therefore, the development of a noncorrosive
decontaminant, sufficiently viscous to resist dripping from the contaminated
surface, is necessary. In the present paper we studied different polysaccharides-thickened
fluoride aqueous solutions as noncorrosive decontaminants for rapid
and efficient VX degradation to the nontoxic product EMPA (ethyl methylphosphonic
acid). Polysaccharides are environmentally benign, natural, and inexpensive.
Other known decontaminants cannot be thickened by polysaccharides,
due to the sensitivity of the latter toward basic or oxidizing agents.
We found that the efficiency of VX degradation in these viscous solutions
in terms of kinetics and product identity is similar to that of KF
aqueous solutions. Guar gum (1.5 wt %) with 4 wt % KF was chosen for
further evaluation. The benign nature, rheological properties, adhering
capabilities to different surfaces, and decontamination from a porous
matrix were examined. This formulation showed promising properties
for implementation as a spray decontaminant for common and sensitive
environmental surfaces
Solvent Effects on the Reactions of the Nerve Agent VX with KF/Al<sub>2</sub>O<sub>3</sub>: Heterogeneous or Homogeneous Decontamination?
Solvent effects on the reactions
of the extremely toxic nerve agent
VX with KF/Al<sub>2</sub>O<sub>3</sub> powder were explored. Small
quantities of water or methanol (5–10 wt %), which effectively
mobilized all components while maintaining the heterogeneous nature
of the reaction, promoted much faster rates than those obtained with
larger quantities. Any amount of acetonitrile resulted in extremely
slow transformations. Surprisingly, 5–50 wt % of heptane led
to fast reactions due to the combination of its ability to mediate
fast diffusion of VX and a MAS centrifugation effect
Hydrothermal Degradation of Chemical Warfare Agents on Activated Carbon: Rapid Chemical-Free Decontamination
Hydrothermal
treatment of activated carbon contaminated with adsorbed
HD, VX, or sarin at temperatures of 90–120 °C decomposes
>95% of the adsorbed chemical warfare agents within a period of
0.5–4
h, in an environmentally friendly route that is free of corrosive
chemicals and ends in nontoxic products
VX Fate on Common Matrices: Evaporation versus Degradation
A study of the volatilization rate of the nerve agent
VX (<i>O</i>-ethyl <i>S</i>-2-(<i>N</i>,<i>N</i>-diisopropylamino)Âethyl methylphosphonothiolate)
from various
urban matrices in a specially designed climatic chamber (model system)
is described. The performance of the model system combined with the
analytical procedure produced profiles of vapor concentration obtained
from samples of VX dispersed as small droplets on the surfaces of
the matrices. The results indicated that the bitumen-containing surfaces
such as asphalt blocks and bitumen sheets conserve VX and slow-release
part of it over a long period of time. No complete mass balance could
be obtained for these surfaces. Influence of environmental and experimental
parameters as well as the efficacy of decontamination procedure were
also measured. From smooth surface tiles a fast release of VX was
measured and almost a complete mass balance was obtained, which characterizes
the behavior of inert surfaces. Experiments carried out on concrete
blocks showed fast decay of the concentration profile along with a
very poor reconstruction of the initial quantity of VX, implying that
this matrix degraded VX actively due to its multiple basic catalytic
sites. To complement this study, solid-state NMR measurements were
compared to add data concerning agent-fate within the matrices