Volume 56, Issue 5 pp. 1143-1149
PAPER
CRIMINALISTICS

Sulfuric, Hydrochloric, and Nitric Acid-Catalyzed Triacetone Triperoxide (TATP) Reaction Mixtures: An Aging Study

Mark Fitzgerald Ph.D.

Mark Fitzgerald Ph.D.

Weapons System Division, Defence Science and Technology Organisation, West Avenue, Edinburgh, South Australia 5111, Australia.

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Daniel Bilusich Ph.D.

Daniel Bilusich Ph.D.

Land Operations Division, Defence Science and Technology Organisation, West Avenue, Edinburgh, South Australia 5111, Australia.

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First published: 19 May 2011
Citations: 16
Additional information and reprint requests:
Mark Fitzgerald, Ph.D.
Explosives & Pyrotechnics Group Defence Science Technology Organisation
Weapons Systems Division (307 EOP)
PO Box 1500
Edinburgh
South Australia 5111
Australia
E-mail: [email protected]

Abstract

Abstract: The organic peroxide explosive triacetone triperoxide (TATP) is regularly encountered by law enforcement agents in various stages of its production. This study utilizes solid-phase microextraction (SPME) and gas chromatography/mass spectrometry (GC/MS) to examine sulfuric acid-, hydrochloric acid-, and nitric acid-catalyzed TATP syntheses during the initial 24 h of these reactions at low temperatures (5–9°C). Additionally, aging of the reaction mixtures was examined at both low and ambient temperatures (19–21°C) for a further 9 days. For each experiment, TATP could be readily identified in the headspace above the reaction mixture 1 h subsequent to the combination of reagents; at 24 h, TATP and diacetone diperoxide (DADP) were prominent. TATP degraded more rapidly than DADP. Additionally, chlorinated acetones chloroacetone and 1,1,-dichloroacetone were identified in the headspace above the hydrochloric acid-catalyzed TATP reaction mixture. These were not present when the catalyst was sulfuric acid or nitric acid.

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