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Lead(II) azide

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Lead(II) azide is a powerful inorganic compound used in explosives. It typically appears as a white to buff colored powder. This substance is much more explosive than other types of azides. Its primary role is to act as an initiator. It is used in detonators to trigger secondary explosives. Because it is so reactive, it requires very careful handling and storage.

The creation of lead(II) azide involves a specific chemical reaction. Scientists prepare it by reacting sodium azide with lead(II) nitrate. This reaction takes place within an aqueous solution, which is a water-based liquid. Lead(II) acetate can also be used as a starting material for this process. To make the final product safer, workers often add thickeners. These thickeners include substances like dextrin or polyvinyl alcohol. These additives help to stabilize the precipitated product. In many cases, the powder is shipped in a dextrinated solution to lower its sensitivity.

Lead(II) azide is characterized by its extreme sensitivity to external stimuli. It can undergo a full detonation after a fall of only 150 mm. A very small static discharge of 7 millijoules is also enough to cause an explosion. It also exhibits a property called immediate deflagration to detonation transition, or DDT. This means that even small amounts undergo a full detonation after being hit by flame or static electricity. To manage these risks, it is usually stored under water. It is also kept in insulated rubber containers to prevent accidental triggers.

The history of this compound shows how science has adapted to military needs. Theodor Curtius first prepared lead azide in its pure form in 1891. By the 1920s and 1930s, researchers developed the dextrinated form known as MIL-L-3055. The DuPont Co began large-scale production of this version in 1932. During World War II, the military required a version with a more brisant output. Brisant refers to the shattering power of an explosive. This led to the development of RD-1333 lead azide. This specific version uses sodium carboxymethyl cellulose as a precipitating agent.

As wars progressed, the demand for lead azide changed again. The Vietnam War caused an accelerated need for the substance. During this time, Special Purpose Lead Azide, or MIL-L-14758, was developed. The United States government also began stockpiling the compound in very large quantities. However, use of lead azide decreased dramatically after the Vietnam War ended. Because the existing US stockpile was so large, domestic manufacture ceased by the early 1990s. In the 2000s, the government investigated ways to dispose of these aging stockpiles. They also looked for new manufacturers to handle the material.

Chemical reactions with other metals can make lead(II) azide even more dangerous. It reacts with metals such as copper, zinc, or cadmium. These reactions form other types of azides. For example, reacting with copper creates copper azide. Copper azide is even more explosive than lead(II) azide. It is considered too sensitive to be used for commercial purposes. If small quantities of lead(II) azide need to be destroyed, ammonium acetate or sodium dichromate are used.

Lead(II) azide has appeared in notable historical events involving firearms. In 1981, John Hinckley Jr. used a Röhm RG-14 revolver to attempt to assassinate President Ronald Reagan. He fired six .22 caliber Devastator rounds. These specific rounds contained lead azide centers. They also featured aluminum tips that were sealed with lacquer. These tips were designed to explode upon impact with a target. One bullet struck White House press secretary James Brady in the head. There is a strong probability that this bullet exploded. The other bullets that hit people did not explode.

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