Literature DB >> 10631666

Characterization of VX on concrete using ion trap secondary ionization mass spectrometry.

G S Groenewold1, A D Appelhans, G L Gresham, J E Olson, M Jeffery, M Weibel.   

Abstract

The nerve agent VX (O-ethyl S-2-diisopropylaminoethyl methyl phosphonothiolate) was analyzed on the surface of concrete samples using an ion trap secondary ion mass spectrometer (IT-SIMS). It was found that VX could be detected down to an absolute quantity of 5 ng on a concrete chip, or to a surface coverage of 0.0004 monolayers on crushed concrete. To achieve these levels of detection, the m/z 268-->128 ion fragmentation was measured using MS2, where m/z 268 corresponds to [VX + H]+, and 128 corresponds to a diisopropylvinylammonium isomer, that is formed by the elimination of the phosphonothiolate moiety. Detection at these levels was accomplished by analyzing samples that had been recently exposed to VX, i.e., within an hour. When the VX-exposed concrete samples were aged, the SIMS signature for intact VX had disappeared, which signaled the degradation of the compound on the concrete surface. The VX signature was replaced by ions which are interpreted in terms of VX degradation products, which appear to be somewhat long lived on the concrete surface. These compounds include ethylmethylphosphonic acid (EMPA), diisopropyl taurine (DIPT), diisopropylaminoethanethiol (DESH), bis(diisopropylaminoethane) disulfide [(DES)2], and a particularly tenacious compound that may correspond to diisopropylvinylamine (DIVA), or an isomer thereof. It was found that the thiolamine-derived degradation products DIPT, DESH, and (DES)2 were removed with isopropyl alcohol extraction. However, the DIVA-related degradation product was observed to strongly adhere to the concrete surface for longer than one week. Although quantitation was not possible in this set of experiments, the results clearly show the rapid degradation of VX on concrete, as well as the surface sensitivity of the IT-SIMS for intact VX and its adsorptive degradation products.

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Year:  2000        PMID: 10631666     DOI: 10.1016/S1044-0305(99)00118-X

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  7 in total

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Authors:  W H Griest; R S Ramsey; C H Ho; W M Caldwell
Journal:  J Chromatogr       Date:  1992-05-29

2.  Detection of 2-chloroethyl ethyl sulfide and sulfonium ion degradation products on environmental surfaces using static SIMS.

Authors:  G S Groenewold; J C Ingram; A D Appelhans; J E Delmore; D A Dahl
Journal:  Environ Sci Technol       Date:  1995-08-01       Impact factor: 9.028

3.  Static secondary ionization mass spectrometry detection of cyclohexylamine on soil surfaces exposed to laboratory air.

Authors:  G S Groenewold; J C Ingrain; A K Gianotto; A D Appelhans; J E Delmore
Journal:  J Am Soc Mass Spectrom       Date:  1996-02       Impact factor: 3.109

Review 4.  Chromatography and mass spectrometry of chemical warfare agents, toxins and related compounds: state of the art and future prospects.

Authors:  C E Kientz
Journal:  J Chromatogr A       Date:  1998-07-24       Impact factor: 4.759

5.  Analysis of VX on soil particles using ion trap secondary ion mass spectrometry.

Authors:  G S Groenewold; A D Appelhans; G L Gresham; J E Olson; M Jeffery; J B Wright
Journal:  Anal Chem       Date:  1999-07-01       Impact factor: 6.986

6.  Static secondary ionization mass spectrometry analysis of tributyl phosphate on mineral surfaces: Effect of Fe(II).

Authors:  G S Groenewold; J C Ingram; J E Delmore; A D Appelhans
Journal:  J Am Soc Mass Spectrom       Date:  1995-03       Impact factor: 3.109

7.  Detection of 2-chloroethylethyl sulfide on soil particles using ion trap-secondary ion mass spectrometry.

Authors:  G S Groenewold; A D Appelhans; J C Ingram; G L Gresham; A K Gianotto
Journal:  Talanta       Date:  1998-11       Impact factor: 6.057

  7 in total

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