Ion Mobility Spectrometry - High Resolution LTQ-Orbitrap Mass Spectrometry for Analysis of Homemade Explosives

被引:21
作者
Hagan, Nathan [1 ]
Goldberg, Ilana [1 ]
Graichen, Adam [2 ]
St Jean, Amanda [1 ]
Wu, Ching [2 ]
Lawrence, David [1 ]
Demirev, Plamen [1 ]
机构
[1] Johns Hopkins Univ, Appl Phys Lab, 11100 Johns Hopkins Rd, Laurel, MD 20723 USA
[2] Excellims Corp, 20 Main St,Acton, Acton, MA 01720 USA
关键词
Homemade explosive; ETN; Ion mobility; Mass spectrometry; ETD; COMPLEX MIXTURE ANALYSIS; GAS-PHASE; TRACE DETECTOR; CORONA DISCHARGE; IONIZATION; CHROMATOGRAPHY; SEPARATION; MS; TETRANITRATE; PERFORMANCE;
D O I
10.1007/s13361-017-1666-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The detailed chemical characterization of homemade explosives (HMEs) and other chemicals that can mimic or mask the presence of explosives is important for understanding and improving the performance of commercial instrumentation used for explosive detection. To that end, an atmospheric-pressure drift tube ion mobility spectrometry (IMS) instrument has been successfully coupled to a commercial tandem mass spectrometry (MS) system. The tandem MS system is comprised of a linear ion trap and a high resolution Orbitrap analyzer. This IMS-MS combination allows extensive characterization of threat chemical compounds, including HMEs, and complex real-world background chemicals that can interfere with detection. Here, the composition of ion species originating from a specific HME, erythritol tetranitrate, has been elucidated using accurate mass measurements, isotopic ratios, and tandem MS. Gated IMS-MS and high-resolution MS have been used to identify minor impurities that can be indicative of the HME source and/or synthesis route. Comparison between data obtained on the IMS/MS system and on commercial stand-alone IMS instruments used as explosive trace detectors (ETDs) has also been performed. Such analysis allows better signature assignments of threat compounds, modified detection algorithms, and improved overall ETD performance.
引用
收藏
页码:1531 / 1539
页数:9
相关论文
共 46 条
[1]   Multiplexed ion mobility spectrometry-orthogonal time-of-flight mass spectrometry [J].
Belov, Mikhail E. ;
Buschbach, Michael A. ;
Prior, David C. ;
Tang, Keqi ;
Smith, Richard D. .
ANALYTICAL CHEMISTRY, 2007, 79 (06) :2451-2462
[2]   Biomolecule Analysis by Ion Mobility Spectrometry [J].
Bohrer, Brian C. ;
Mererbloom, Samuel I. ;
Koeniger, Stormy L. ;
Hilderbrand, Amy E. ;
Clemmer, David E. .
ANNUAL REVIEW OF ANALYTICAL CHEMISTRY, 2008, 1 (01) :293-327
[3]   GAS-PHASE ION CHROMATOGRAPHY - TRANSITION-METAL STATE SELECTION AND CARBON CLUSTER FORMATION [J].
BOWERS, MT ;
KEMPER, PR ;
VON HELDEN, G ;
VANKOPPEN, PAM .
SCIENCE, 1993, 260 (5113) :1446-1451
[4]  
Clemmer DE, 1997, J MASS SPECTROM, V32, P577
[5]   Mass analysis of mobility-selected ion populations using dual gate, ion mobility, quadrupole ion trap mass spectrometry [J].
Clowers, BH ;
Hill, HH .
ANALYTICAL CHEMISTRY, 2005, 77 (18) :5877-5885
[6]   Ion mobility spectrometry rediscovered [J].
Cottingham, K .
ANALYTICAL CHEMISTRY, 2003, 75 (19) :435A-439A
[7]   Evaluation of false positive responses by mass spectrometry and ion mobility spectrometry for the detection of trace explosives in complex samples [J].
Crawford, C. L. ;
Hill, H. H., Jr. .
ANALYTICA CHIMICA ACTA, 2013, 795 :36-43
[8]   Comparison of reactant and analyte ions for 63Nickel, corona discharge, and secondary electrospray ionization sources with ion mobility-mass spectrometry [J].
Crawford, C. L. ;
Hill, H. H. .
TALANTA, 2013, 107 :225-232
[9]   Accurate and reproducible ion mobility measurements for chemical standard evaluation [J].
Crawford, C. L. ;
Hauck, B. C. ;
Tufariello, J. A. ;
Harden, C. S. ;
McHugh, V. ;
Siems, W. F. ;
Hill, H. H., Jr. .
TALANTA, 2012, 101 :161-170
[10]   Review on Ion Mobility Spectrometry. Part 2: hyphenated methods and effects of experimental parameters [J].
Cumeras, R. ;
Figueras, E. ;
Davis, C. E. ;
Baumbach, J. I. ;
Gracia, I. .
ANALYST, 2015, 140 (05) :1391-1410