Insight into electrostatic initiation of nitramine explosives
Related Experiment Video
Updated: Mar 10, 2026

Research and Development of High-performance Explosives
Published on: February 20, 2016
Bisheng Tan1, Zhipeng Li2, Xudong Guo2
1Institute of Chemical Materials, China Academy of Engineering Physics (CAEP), Mailbox 919, Branch Box 311, Mianyang, 621900, People's Republic of China. tanbs_my@caep.cn.
Abstract:
The electrostatic safety of explosives is of great importance. However, the mechanism for the transfer of energy from an electrostatic spark to the reactive center of an explosive material is not well understood. Thus, in this work, we attempted to clarify the mechanism associated with the static-electricity-initiated detonation of explosives using a model of the interaction that incorporated relevant parameters. Nitramine explosives were considered as examples to study the relationship between electrostatic spark energy and 32 relevant parameters. The four parameters that were most closely correlated with the electrostatic spark energy were the standard deviation of the negative electrostatic potential, the minimum surface electrostatic potential, the minimum ionization energy, and the detonation pressure. A model for the dependence of the electrostatic spark energy on these four parameters was derived using the theoretical method known as genetic function approximation. The electrostatic spark energy values predicted using this model were in good agreement with the corresponding experimental values. The results of this work should lead to a deeper understanding of the electrostatic initiation mechanism of nitramines, and help to inspire the design of new explosives.
Related Concept Videos
2° Amines to N-Nitrosamines: Reaction with NaNO2
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Preparation of Nitriles
Electrophilic Aromatic Substitution: Nitration of Benzene

