Related Experiment Video
Updated: Mar 1, 2026

Laboratory Scale Slow Cook-Off Testing of Rocket Propellants: The Combustion Rate Analysis of a Slowly Heated Propellant CRASH-P Test
Published on: February 6, 2021
Leaching of propellant compounds from munition residues may be controlled by sorption to nitrocellulose
Dave T F Kuo1, Michael Simini2, Herbert E Allen3
1Department of Architecture and Civil Engineering, City University of Hong Kong, Kowloon City, Hong Kong; City University of Hong Kong Shenzhen Research Institute, Shenzhen 518057, China.
Abstract:
Sustainable management of military ranges requires effective assessment of surface mobility and leaching potential of propellant compounds (PCs). Previous studies have focused mostly on PCs' dissolution from fired residues and their sorption to soil components. This work investigated the potential role of nitrocellulose, a major component in propellants, in the binding of PCs to propellant residues. Sorption isotherms of military grade nitrocellulose for dissolved nitroglycerine (NG) or 2,4-dinitrotoluene (2,4-DNT) was measured in batch experiments and were determined to be SNG=102.39(±0.05)CNG0.916(±0.032) and S2,4-DNT=103.08(±0.01)C2,4-DNT0.668(±0.010) (S and C in mg/kgnitrocellulose and mg/Lwat, respectively). Solid-to-water partitioning for NG and 2,4-DNT was 100 times greater in propellant residues than in typical military ranges soils. Since nitrocellulose can sorb NG and 2,4-DNT up to 23 and 5% of its mass, respectively, it can slow down, through retarded diffusion, the leaching of PCs from fired residues over the typical composition ranges of common propellants. The slow leaching of PCs from propellant grains in column studies can be better interpreted by considering their sorptive interaction with nitrocellulose in addition to dissolution kinetics. With nitrocellulose as the carrying matrix, residue-bound PCs may migrate farther and persist longer in subsurface environment.
Related Concept Videos
2° Amines to N-Nitrosamines: Reaction with NaNO2
The Equilibrium Constant
Preparation of Nitriles
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...
Nitrosation of Enols

