Identification of Inorganic Improvised Explosive Devices Using Sequential Injection Capillary Electrophoresis and Contactless Conductivity Detection

被引:60
作者
Blanco, Gustavo A. [1 ]
Nai, Yi H. [1 ]
Hilder, Emily F. [1 ]
Shellie, Robert A. [1 ]
Dicinoski, Greg W. [1 ]
Haddad, Paul R. [1 ]
Breadmore, Michael C. [1 ]
机构
[1] Univ Tasmania, Australian Ctr Res Separat Sci, Sch Chem, Fac Sci Engn & Technol, Hobart, Tas 7001, Australia
基金
澳大利亚研究理事会;
关键词
ZONE-ELECTROPHORESIS; ION CHROMATOGRAPHY; POSTBLAST RESIDUES; FLOW-INJECTION; MICROCHIP ELECTROPHORESIS; ANIONS; SEPARATION; CATIONS; SYSTEM; INSTRUMENTATION;
D O I
10.1021/ac2020195
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple sequential injection capillary electrophoresis (SI-CE) instrument with capacitively coupled contactless conductivity detection ((CD)-D-4) has been developed for the rapid separation of anions relevant to the identification of inorganic improvised explosive devices (IEDs). Four of the most common explosive tracer ions, nitrate, perchlorate, chlorate, and azide, and the most common background ions, chloride, sulfate, thiocyanate, fluoride, phosphate, and carbonate, were chosen for investigation. Using a separation electrolyte comprising 50 mM tris(hydroxymethyl)aminomethane, 50 mM cyclohexyl-2-aminoethanesulfonic acid, pH 8.9 and 0.05% poly(ethyleneimine) (PEI) in a hexadimethrine bromide (HDMB)-coated capillary it was possible to partially separate all 10 ions within 90 s. The combination of two cationic polymer additives (PEI and HDMB) was necessary to achieve adequate selectivity with a sufficiently stable electroosmotic flow (EOF), which was not possible with only one polymer. Careful optimization of variables affecting the speed of separation and injection timing allowed a further reduction of separation time to 55 s while maintaining adequate efficiency and resolution. Software control makes high sample throughput possible (60 samples/h), with very high repeatability of migration times [0.63-2.07% relative standard deviation (RSD) for 240 injections]. The separation speed does not compromise sensitivity, with limits of detection ranging from 23 to 50 mu g.L-1 for all the explosive residues considered, which is 10 x lower than those achieved by indirect absorbance detection and 2 x lower than those achieved by (CD)-D-4 using portable benchtop instrumentation. The combination of automation, high sample throughput, high confidence of peak identification, and low limits of detection makes this methodology ideal for the rapid identification of inorganic IED residues.
引用
收藏
页码:9068 / 9075
页数:8
相关论文
共 40 条
[1]  
Bowser MT, 2001, ELECTROPHORESIS, V22, P3668, DOI 10.1002/1522-2683(200109)22:17<3668::AID-ELPS3668>3.0.CO
[2]  
2-M
[3]  
Breadmore MC, 2000, ELECTROPHORESIS, V21, P3181, DOI 10.1002/1522-2683(20000901)21:15<3181::AID-ELPS3181>3.0.CO
[4]  
2-L
[5]   INFLUENCE OF ANALYTE PLUG WIDTH ON PLATE NUMBER IN CAPILLARY ELECTROPHORESIS [J].
DELINGER, SL ;
DAVIS, JM .
ANALYTICAL CHEMISTRY, 1992, 64 (17) :1947-1959
[6]   Novel electrolyte for the analysis of cations in low explosive residue by capillary electrophoresis [J].
Doyle, JM ;
McCord, BR .
JOURNAL OF CHROMATOGRAPHY B, 1998, 714 (01) :105-111
[7]   Combination of flow injection with capillary electrophoresis .1. The basic system [J].
Fang, ZL ;
Liu, ZS ;
Shen, Q .
ANALYTICA CHIMICA ACTA, 1997, 346 (02) :135-143
[8]   Use of ionic polymers as stationary and pseudo-stationary phases in the separation of ions by capillary electrophoresis and capillary electrochromatography [J].
Fritz, JS ;
Breadmore, MC ;
Hilder, EF ;
Haddad, PR .
JOURNAL OF CHROMATOGRAPHY A, 2002, 942 (1-2) :11-32
[9]   Capillaries modified by polyelectrolyte multilayers for electrophoretic separations [J].
Graul, TW ;
Schlenoff, JB .
ANALYTICAL CHEMISTRY, 1999, 71 (18) :4007-4013
[10]   EXPLOSIVE RESIDUE ANALYSIS BY CAPILLARY ELECTROPHORESIS AND ION CHROMATOGRAPHY [J].
HARGADON, KA ;
MCCORD, BR .
JOURNAL OF CHROMATOGRAPHY, 1992, 602 (1-2) :241-247