Related Experiment Video
Updated: Jan 10, 2026

A General Method for Detecting Nitrosamide Formation in the In Vitro Metabolism of Nitrosamines by Cytochrome P450s
Published on: September 25, 2017
Treatment of Xenobiotic Cyclic Nitramine Explosives in Wastewater
1Department of Environmental Hydrology and Microbiology, The Zuckerberg Institute for Water Research, The Jacob Blauste Institute for Desert Research, Ben-Gurion University of the Negev, Midreshet Ben-Gurion 8499000, Israel.
Abstract:
Cyclic nitramine explosives such as octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), and 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20) are xenobiotics that are utilized in a variety of propellants and traditional weapons. The primary source of water contamination is the industrial use of these hazardous substances in propellants and wastewater generated from munitions production facilities. These chemicals have a negative impact on human health and ecosystems. It is necessary to remove these toxic compounds from the environment safely because their production and usage have seriously contaminated soil and groundwater. Although there are no widely adopted WHO or US federal Maximum Contaminant Levels (MCLs) for military explosives, the health advisory limits for RDX in drinking water are 2 µg/L, and for HMX are 400 µg/L. Numerous traditional treatment approaches that incorporate physical, biological, and chemical processes have been used to decontaminate explosive wastewater. However, contaminants are not completely mineralized by these methods. Complete reduction of these chemicals can be accomplished by combining suitable methods. For the remediation of explosive effluent, integrated treatment systems that combine the effectiveness of biological and physical-chemical methods have shown promising results. This review discusses the toxicity and some physical-chemical-biological and combined treatment processes of wastewater polluted by these explosive contaminants.
Related Concept Videos
2° Amines to N-Nitrosamines: Reaction with NaNO2
Enhanced Elimination of Poison
Antidotes serve a crucial role in counteracting the effects of poison by inhibiting enzymes responsible for producing harmful drug metabolites. In some cases, these toxic metabolites can be neutralized by endogenous cosubstrates, which are maintained at specific concentrations to prevent interaction with cellular macromolecules and subsequent cell death.
Renal excretion is the...
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Physical Properties of Amines
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...

