CE and CEC
Identification of inorganic ions in post-blast explosive residues using portable CE instrumentation and capacitively coupled contactless conductivity detection
Article first published online: 26 NOV 2008
DOI: 10.1002/elps.200800226
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Hutchinson, J. P., Johns, C., Breadmore, M. C., Hilder, E. F., Guijt, R. M., Lennard, C., Dicinoski, G. and Haddad, P. R. (2008), Identification of inorganic ions in post-blast explosive residues using portable CE instrumentation and capacitively coupled contactless conductivity detection. ELECTROPHORESIS, 29: 4593–4602. doi: 10.1002/elps.200800226
Publication History
- Issue published online: 26 NOV 2008
- Article first published online: 26 NOV 2008
- Manuscript Accepted: 27 MAY 2008
- Manuscript Revised: 12 MAY 2008
- Manuscript Received: 7 APR 2008
Funded by
- National Security Science & Technology Unit
- Department of Prime Minister and Cabinet
- National Institute for Forensic Science
- Abstract
- Article
- References
- Cited By
Keywords:
- Contactless conductivity detection;
- Homemade explosive devices;
- Inorganic anions and cations;
- Portable CE;
- Post-blast residues
Abstract
Novel CE methods have been developed on portable instrumentation adapted to accommodate a capacitively coupled contactless conductivity detector for the separation and sensitive detection of inorganic anions and cations in post-blast explosive residues from homemade inorganic explosive devices. The methods presented combine sensitivity and speed of analysis for the wide range of inorganic ions used in this study. Separate methods were employed for the separation of anions and cations. The anion separation method utilised a low conductivity 70 mM Tris/70 mM CHES aqueous electrolyte (pH 8.6) with a 90 cm capillary coated with hexadimethrine bromide to reverse the EOF. Fifteen anions could be baseline separated in 7 min with detection limits in the range 27–240 μg/L. A selection of ten anions deemed most important in this application could be separated in 45 s on a shorter capillary (30.6 cm) using the same electrolyte. The cation separation method was performed on a 73 cm length of fused-silica capillary using an electrolyte system composed of 10 mM histidine and 50 mM acetic acid, at pH 4.2. The addition of the complexants, 1 mM hydroxyisobutyric acid and 0.7 mM 18-crown-6 ether, enhanced selectivity and allowed the separation of eleven inorganic cations in under 7 min with detection limits in the range 31–240 μg/L. The developed methods were successfully field tested on post-blast residues obtained from the controlled detonation of homemade explosive devices. Results were verified using ion chromatographic analyses of the same samples.

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