| Vx (nerve Agent) |
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Information AboutVx (nerve Agent) |
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VX is one of the most toxic nerve agents ever synthesized.1 The VX Nerve Agent is the most well-known of the V-series Of Nerve Agents . Its chemical name is O-ethyl-S- {Link without Title} methylphosphonothiolate and its Molecular Formula is C11H26NO2PS. The chemist Ranajit Ghosh discovered the V-series nerve agents at the government research establishment at Porton Down , England in 1952 ; VX was passed over in favour of continuing with Sarin as the UK chemical weapon of choice. VX agent is considered an Area Denial Weapon due to its physical properties. With its high Viscosity and low Volatility , VX has the texture and feel of high-grade motor oil. This makes it especially dangerous, as it has a high persistence in the environment. It is odourless and tasteless, and can be distributed as a liquid or, through evaporation, into small amounts of vapour. It works as a nerve agent by blocking the function of the Enzyme Acetylcholinesterase . Normally, an electric nerve pulse would cause the release of Acetylcholine over a Synapse that would stimulate muscle contraction. The acetylcholine is then broken down to non-reactive substances ( Acetic Acid and Choline ) by the acetylcholinesterase enzyme. If more muscle tension is needed the nerve must release more acetylcholine. VX blocks the action of acetylcholinesterase, thus resulting in sustained contractions of all the muscles in the body. Sustained contraction of the diaphragm muscle causes death by asphyxiation. As little as 200 micrograms is enough to kill an average person, depending on method of absorption. If the absorbed dose is not too high, death can be avoided if the appropriate antidote is injected immediately after exposure. The most commonly used antidotes are Atropine , Pralidoxime , and Diazepam which are, in several nations, issued for military personnel in the form of an Autoinjector . Atropine works by binding and blocking a subset of acetylcholine receptors (known as Muscarinic Acetylcholine Receptor , mAchR), so that the build up of acetylcholine produced by loss of the acetylcholinesterase function can no longer affect their target. The injection of pralidoxime regenerates bound acetylcholinesterase. SYNTHESIS VX is produced via the "Transester Process". This entails a complex chemical transition whereby Phosphorus Trichloride is methylated to produce methyl phosphonous dichloride. The resulting material is reacted with ethanol to form a diester. This is then Transesterified to produce the immediate precursor of VX. Finally, the immediate precursor is reacted with sulfur to form V-agent. VX can also be delivered in binary chemical weapons which mix in-flight to form the agent prior to release. Binary VX is referred to as VX2, and is created by mixing O-(2-diisopropylaminoethyl) O'-ethyl methylphosphonite (Agent QL) with elemental sulfur (Agent NE) as is done in the BIGEye aerial chemical bomb. It may also be produced by mixing with sulfur compounds, as with the liquid dimethyl polysulfide mixture (Agent NM) in the cancelled XM-768 8-inch binary projectile program. SOLVOLYSIS Like other Organophosphorus nerve agents, VX may be destroyed by reaction with strong nucleophiles such as Pralidoxime . The reaction of VX with concentrated aqueous sodium hydroxide results in competing cleavage of the P-O and P-S esters, with P-S cleavage dominating. This is somewhat problematic, since the product of P-O bond cleavage (named EA 2192) remains toxic. In contrast, reaction with the anion of hydrogen peroxide (hydroperoxidolysis) leads to exclusive cleavage of the P-S bond.5 HISTORY Despite creating the agent, the United Kingdom unilaterally renounced chemical and biological weapons in 1956. In 1958 the British government traded their research on VX technology with the United States Of America in exchange for information on Thermonuclear Weapons . The US then went into production of large amounts of VX in 1961 . The US later started the destruction of its stockpiles of the nerve agents (by Incineration at Johnston Island in the North Pacific), as mandated by the US accession to the Chemical Weapons Convention . Earlier, pre-treaty disposal included the US Army's CHASE (Cut Holes And Sink 'Em) program, in which old ships were filled with chemical weapons stockpiles and then Scuttled . CHASE 8 was conducted on June 15, 1967, in which the S.S. ''Cpl. Eric G. Gibson'' was filled with 7,380 VX rockets and scuttled in 7,200 feet of water, off the coast of Atlantic City, New Jersey . VX hydrolysis began on May 5 2005 and as of June 12 the facility had destroyed 2,894 US gallons (11 m³) of VX. A contained spill of 30 US gallons (100 L) drew attention to the disposal process, but authorities said no agent was released and no one was injured in the spill. indicates that Iraq had indeed weaponized VX in 1988 and had dropped three VX-filled bombs on Iran . {Link without Title} On January 5, 2007, DuPont announced they had abandoned plans to seek the contract for transportation, treatment, and disposal of VX at their Chambersworks Secure Treatment Facility in Deepwater, NJ. They cited lengthy review processes and strong opposition by New Jersey's governor, Jon Corzine, New Jersey senators and congressmen, and environmental groups including NJ Audubon, Delaware Riverkeepers, and the Litoral Society as well as the on-going investigation by the GAO as factors in their decision to withdraw from the plan. IN POPULAR CULTURE See Also: Nerve agents#Popular culture l1=Nerve agents in popular culture REFERENCES EXTERNAL LINKS
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