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Lead(II) azide facts for kids

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Lead(II) azide
Lead(II)azide.svg
Lead azide (modified beta) 01.JPG
IUPAC name Diazidolead
Identifiers
CAS number 13424-46-9
PubChem 61600
EC number 236-542-1
SMILES [N-]=[N+]=N[Pb]N=[N+]=[N-]
Properties
Molecular formula
Molar mass 0 g mol-1
Appearance White powder
Density 4.71 g/cm3
Melting point
2.3 g/100 mL (18 °C)
9.0 g/100 mL (70 °C)
Solubility Very soluble in acetic acid
Insoluble in ammonia solution, NH4OH
Thermochemistry
Std enthalpy of
formation ΔfHo298
462.3 kJ/mol
Explosive data
Shock sensitivity High
Friction sensitivity High
Detonation velocity 5180 m/s
Hazards
Main hazards Harmful, explosive
NFPA 704

NFPA 704.svg

0
3
4
 
Related compounds
Other cations Potassium azide
Sodium azide
Copper(II) azide
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)

Lead(II) azide (chemical formula: Pb(N
3
)
2
) is a type of inorganic compound. It is much more explosive than other similar chemicals called azides. Because it is so explosive, Pb(N
3
)
2
is used in special devices called detonators. These detonators help to set off other, larger explosives. In its common form, it looks like a white or light brown powder.

How Lead Azide is Made

Lead(II) azide is made by mixing two other chemicals. These are sodium azide and lead(II) nitrate. This mixing happens in water. Sometimes, lead(II) acetate can be used instead of lead(II) nitrate.

To make the product safer and more stable, other substances are often added. These can be thickeners like dextrin or polyvinyl alcohol. These additions help to make the lead azide less sensitive. It is often sent out while still mixed in a dextrinated solution. This makes it safer to handle.

History of Production

A scientist named Theodor Curtius first made pure lead azide in 1891. However, it was very sensitive and hard to handle. So, in the 1920s and 1930s, a safer version was created. This version was mixed with dextrin (MIL-L-3055). The DuPont Company started making it in large amounts in 1932.

During World War II, there was a need for an even more powerful type of lead azide. This led to the development of RD-1333 lead azide (MIL-DTL-46225). This version used sodium carboxymethyl cellulose to help it form. Later, during the Vietnam War, a special type called Special Purpose Lead Azide (MIL-L-14758) was made. The US government also started storing large amounts of it.

After the Vietnam War, less lead azide was needed. By the early 1990s, the US stopped making it because they had so much stored. In the 2000s, people worried about how old the stored lead azide was. They started looking for ways to safely get rid of it and find new companies to make it.

Explosive Features

Lead azide is very sensitive. This means it can explode easily. Because of this, it is usually kept and handled under water. It is stored in special rubber containers that protect it.

It can explode if it falls about 150 millimeters (6 inches). It can also explode from a small spark of static electricity. Its explosion speed is very fast, around 5,180 meters per second (17,000 feet per second).

Small amounts of lead azide can be safely destroyed. This is done using chemicals like ammonium acetate and sodium dichromate.

Lead azide has a special quality called "immediate deflagration to detonation transition" (DDT). This means that even a small amount can fully explode. This can happen if it is touched by a flame or static electricity.

Lead azide can react with certain metals. These include copper, zinc, or cadmium. When it reacts, it can form other types of azides. For example, copper azide is even more explosive than lead azide. It is too sensitive to be used safely in products.

Lead azide was part of special bullets used in a shooting event on March 30, 1981. These bullets were designed to explode when they hit something. One of these bullets hit White House press secretary James Brady and likely exploded. Other bullets that hit people, including the one that hit President Ronald Reagan, did not explode.

See also

  • Lead styphnate
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