PETN

PETN (pentaerythritol tetranitrate, also known as pentrite, or rarely and primarily in German as nitropenta) is one of the most powerful high explosives known, with a relative effectiveness factor (R.E. factor) of 1.66. It is more sensitive to shock or friction than TNT or tetryl, and it is never used alone as a booster. It is primarily used in booster and bursting charges of small caliber ammunition, in upper charges of detonators in some land mines and shells, and as the explosive core of detonation cord.

PETN is also used as a vasodilator, similar to Glyceryl trinitrate (pharmacology). The medicine for heart diseases, "Lentonitrat", is pure PETN.^[1]

Additional recommended knowledge

Weighing the right way

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Essential Laboratory Skills Guide

Properties

The velocity of detonation of PETN at a density of 1.7 g/cm³ is 8,400 meters per second. The heat of explosion is 5,862 kilojoules per kilogram^[2], or 1.5 times that of TNT.

PETN's formula is C(CH₂ONO₂)₄. Its theoretical maximum crystal density is 1.773 g/cm³. It melts at 141 °C.

As a pollutant in the environment

PETN does not occur naturally, so the production and use of this kind of compound can lead to contamination of the environment^{[citation needed]}. PETN is subject to biodegradation in untreated or unpreserved urine and feces^{[citation needed]}. There also have been some reports of its degradation by bacteria, whose PETN reductase denitrates PETN into trinitrates and then dinitrates (French et al., 1996). The last compound shown in the pathway, pentaerythritol dinitrate, is degraded further to unknown products^{[citation needed]}.

Production

PETN's preparation involves the nitration of pentaerythritol with a mixture of concentrated nitric and sulfuric acid. The preferred method of nitration is the ICI method, which utilizes concentrated nitric acid (98%+) alone, as mixed acid can create unstable sulfonated by-products.

C(CH₂OH)₄ + 4HNO₃ → C(CH₂ONO₂)₄ + 4H₂O

History

Penthrite was first synthesized in 1891 by Tollens and Wiegand by nitration of pentaerythritol. In 1912, after being patented by the German government, the production of PETN started. PETN was used by the German army in World War I. ^[3] PETN is also one of the ingredients in Semtex plastic explosive.

See also

• Pentolite
• Semtex
• RDX
• TNT

References

• Cooper, Paul W., Explosives Engineering, New York: Wiley-VCH, 1996. ISBN 0-471-18636-8

1. ^ Russek H. I. (1966). "The therapeutic role of coronary vasodilators: glyceryl trinitrate, isosorbide dinitrate, and pentaerythritol tetranitrate.". American Journal of Medical Science 252 (1): 9-20. PMID 4957459.
2. ^ Erich Ammedick: Militärchemie. eine Einführung. 4. Auflage. In: Bausteine der Chemie. VEB Deutscher Verlag für Grundstoffindustrie, Leipzig 1980, ISBN 978-3342000372 (German)
3. ^ Stettbacher, Alfred (1933). Die Schiess- und Sprengstoffe. Barth, 459.