A new method for the determination of the nitrogen content of nitrocellulose based on the molar ratio of nitrite-to-nitrate ions released after alkaline hydrolysis
Creators
- 1. Sorbonne Universités, UPMC Univ Paris 06, LBM, 4 place Jussieu, F-75005 Paris (France)
- 2. CNRS, UMR 7195 PECSA, 11 rue Pierre et Marie Curie, 75005 Paris (France)
- 3. Central Laboratory of Police Prefecture (LCPP), 39 bis rue de Dantzig, 75015 Paris (France)
- 4. PSL Research University, Chimie ParisTech, Laboratory of Physicochemistry of Electrolytes, Colloids and Analytical Sciences (PECSA), 11 rue Pierre et Marie Curie, 75005 Paris (France)
- 5. CNRS, UMR 7203 LBM, F-75005 Paris (France)
- 6. École Normale Supérieure-PSL Research University, Département de Chimie, 24 rue Lhomond, 75005 Paris (France)
Description
Highlights: • New insights into the nitrocellulose alkaline denitration mechanism. • Linear correlation for molar ratio of nitrite-to-nitrate ions and nitrogen content. • Capillary electrophoresis monitoring of nitrite and nitrate ions. • Applications to explosive and non-explosive nitrocellulose-containing samples. • Improved performances (including safety) over classical methods. - Abstract: A new method was proposed to determine the nitrogen content of nitrocelluloses (NCs). It is based on the finding of a linear relationship between the nitrogen content and the molar ratio of nitrite-to-nitrate ions released after alkaline hydrolysis. Capillary electrophoresis was used to monitor the concentration of nitrite and nitrate ions. The influences of hydrolysis time and molar mass of NC on the molar ratio of nitrite-to-nitrate ions were investigated, and new insights into the understanding of the alkaline denitration mechanism of NCs, underlying this analytical strategy is provided. The method was then tested successfully with various explosive and non-explosive NC-containing samples such as various daily products and smokeless gunpowders. Inherently to its principle exploiting a concentration ratio, this method shows very good repeatability in the determination of nitrogen content in real samples with relative standard deviation (n = 3) inferior to 1.5%, and also provides very significant advantages with respect to sample extraction, analysis time (1 h for alkaline hydrolysis, 3 min for electrophoretic separation), which was about 5 times shorter than for the classical Devarda's method, currently used in industry, and safety conditions (no need for preliminary drying NC samples, mild hydrolysis conditions with 1 M sodium hydroxide for 1 h at 60 °C)
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2014.12.032Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2014.12.032;
- PII
- S0304-3894(14)01016-4;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 286
- Journal Page Range
- p. 92-99
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47030825
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ALKALINE HYDROLYSIS; AMINES; BROMIDES; CONCENTRATION RATIO; CORRELATIONS; DENITRATION; DRYING; ELECTROLYTES; ELECTROPHORESIS; EXTRACTION; MOLECULAR IONS; NITRATES; NITRITES; NITROCELLULOSE; NITROGEN; SODIUM HYDROXIDES
- Descriptors DEC
- ALKALI METAL COMPOUNDS; BROMINE COMPOUNDS; CARBOHYDRATES; CELLULOSE ESTERS; CHARGED PARTICLES; CHEMICAL EXPLOSIVES; CHEMICAL REACTIONS; DECOMPOSITION; DIMENSIONLESS NUMBERS; ELEMENTS; ESTERS; EXPLOSIVES; HALIDES; HALOGEN COMPOUNDS; HYDROGEN COMPOUNDS; HYDROLYSIS; HYDROXIDES; IONS; LYSIS; NITRIC ACID ESTERS; NITROGEN COMPOUNDS; NONMETALS; ORGANIC COMPOUNDS; OXYGEN COMPOUNDS; POLYSACCHARIDES; SACCHARIDES; SEPARATION PROCESSES; SODIUM COMPOUNDS; SOLVOLYSIS
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.