A novel method for analysis of explosives residue by simultaneous detection of anions and cations via capillary zone electrophoresis.

Talanta

Graduate and Undergraduate Program, Department of Chemistry and Biochemistry, Ohio University, Athens, OH 45701, USA.

Published: August 2005

AI Article Synopsis

  • A new electrolyte has been created for capillary electrophoresis to separate cations and anions in low explosive residues, using a combination of specific chemicals for enhanced effectiveness.
  • The method allows for simultaneous detection of both ions with impressive limits of detection (0.5 to 5 ppm for anions and 10 to 15 ppm for cations) and can complete the analysis in under 7 minutes.
  • When tested on various explosives like Pyrodex® RS and black powder, this method proved to be faster and more thorough than previous techniques that analyzed anions and cations separately.

Article Abstract

A novel electrolyte has been developed for the simultaneous separation of cations and anions in low explosive residue by capillary electrophoresis. This electrolyte contains 15mM alpha-hydroxyisobutyric acid (HIBA) as the buffer, 6mM imidazole as the cation chromophore, 3mM 1,3,6-naphthalenetrisulfonic acid (NTS) as the anion chromophore, 4mM 18-crown-6 ether as a cation selectivity modifier, and 5% (v/v) acetonitrile as an organic modifier. The pH was adjusted to 6.5 using tetramethylammonium hydroxide (TMAOH), an electroosmotic flow modifier. The method was optimized by varying the concentrations of alpha-HIBA, imidazole, and 1,3,6-NTS at three different pH values. The results provided a simultaneous indirect photometric analysis of both anions and cations with detection limits ranging from 0.5 to 5ppm for anions and from 10 to 15ppm for cations with a total run time of under 7min. The method was then applied to the analysis of Pyrodex((R)) RS and black powder, as well as several smokeless powders. The results obtained were consistent with previously reported results for separate anion and cation analysis and provide a faster, more complete analysis of each sample in a single chromatographic run.

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Source
http://dx.doi.org/10.1016/j.talanta.2005.01.037DOI Listing

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