Applications of Direct Injection Soft Chemical Ionisation-Mass Spectrometry for the Detection of Pre-blast Smokeless Powder Organic Additives

Ramón González-Méndez, Chris A Mayhew

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Analysis of smokeless powders is of interest from forensics and security perspectives. This article reports the detection of smokeless powder organic additives (in their pre-detonation condition), namely the stabiliser diphenylamine and its derivatives 2-nitrodiphenylamine and 4-nitrodiphenylamine, and the additives (used both as stabilisers and plasticisers) methyl centralite and ethyl centralite, by means of swab sampling followed by thermal desorption and direct injection soft chemical ionisation-mass spectrometry. Investigations on the product ions resulting from the reactions of the reagent ions H 3 O + and O 2 + with additives as a function of reduced electric field are reported. The method was comprehensively evaluated in terms of linearity, sensitivity and precision. For H 3 O + , the limits of detection (LoD) are in the range of 41–88 pg of additive, for which the accuracy varied between 1.5 and 3.2%, precision varied between 3.7 and 7.3% and linearity showed R 2 ≥ 0.9991. For O 2 + , LoD are in the range of 72 to 1.4 ng, with an accuracy of between 2.8 and 4.9% and a precision between 4.5 and 8.6% and R 2 ≥ 0.9914. The validated methodology was applied to the analysis of commercial pre-blast gun powders from different manufacturers. [Figure not available: see fulltext.].

Original languageEnglish
Pages (from-to)615-624
Number of pages10
JournalJournal of the American Society for Mass Spectrometry
Volume30
Issue number4
Early online date13 Feb 2019
DOIs
Publication statusPublished - 19 Apr 2019

Fingerprint

Lobeline
Direct injection
Powders
Ionization
Mass spectrometry
Mass Spectrometry
Injections
Limit of Detection
Diphenylamine
Ions
Plasticizers
Firearms
Thermal desorption
Detonation
Hot Temperature
Electric fields
Sampling
Derivatives
N,N'-diethylcarbanilide

Keywords

  • Proton transfer reaction mass spectrometry
  • PTR-MS
  • SCIMS
  • Smokeless powder additives
  • Smokeless powders
  • Soft chemical ionisation-mass spectrometry

ASJC Scopus subject areas

  • Structural Biology
  • Spectroscopy

Cite this

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title = "Applications of Direct Injection Soft Chemical Ionisation-Mass Spectrometry for the Detection of Pre-blast Smokeless Powder Organic Additives",
abstract = "Analysis of smokeless powders is of interest from forensics and security perspectives. This article reports the detection of smokeless powder organic additives (in their pre-detonation condition), namely the stabiliser diphenylamine and its derivatives 2-nitrodiphenylamine and 4-nitrodiphenylamine, and the additives (used both as stabilisers and plasticisers) methyl centralite and ethyl centralite, by means of swab sampling followed by thermal desorption and direct injection soft chemical ionisation-mass spectrometry. Investigations on the product ions resulting from the reactions of the reagent ions H 3 O + and O 2 + with additives as a function of reduced electric field are reported. The method was comprehensively evaluated in terms of linearity, sensitivity and precision. For H 3 O + , the limits of detection (LoD) are in the range of 41–88 pg of additive, for which the accuracy varied between 1.5 and 3.2{\%}, precision varied between 3.7 and 7.3{\%} and linearity showed R 2 ≥ 0.9991. For O 2 + , LoD are in the range of 72 to 1.4 ng, with an accuracy of between 2.8 and 4.9{\%} and a precision between 4.5 and 8.6{\%} and R 2 ≥ 0.9914. The validated methodology was applied to the analysis of commercial pre-blast gun powders from different manufacturers. [Figure not available: see fulltext.].",
keywords = "Proton transfer reaction mass spectrometry, PTR-MS, SCIMS, Smokeless powder additives, Smokeless powders, Soft chemical ionisation-mass spectrometry",
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AU - Mayhew, Chris A

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N2 - Analysis of smokeless powders is of interest from forensics and security perspectives. This article reports the detection of smokeless powder organic additives (in their pre-detonation condition), namely the stabiliser diphenylamine and its derivatives 2-nitrodiphenylamine and 4-nitrodiphenylamine, and the additives (used both as stabilisers and plasticisers) methyl centralite and ethyl centralite, by means of swab sampling followed by thermal desorption and direct injection soft chemical ionisation-mass spectrometry. Investigations on the product ions resulting from the reactions of the reagent ions H 3 O + and O 2 + with additives as a function of reduced electric field are reported. The method was comprehensively evaluated in terms of linearity, sensitivity and precision. For H 3 O + , the limits of detection (LoD) are in the range of 41–88 pg of additive, for which the accuracy varied between 1.5 and 3.2%, precision varied between 3.7 and 7.3% and linearity showed R 2 ≥ 0.9991. For O 2 + , LoD are in the range of 72 to 1.4 ng, with an accuracy of between 2.8 and 4.9% and a precision between 4.5 and 8.6% and R 2 ≥ 0.9914. The validated methodology was applied to the analysis of commercial pre-blast gun powders from different manufacturers. [Figure not available: see fulltext.].

AB - Analysis of smokeless powders is of interest from forensics and security perspectives. This article reports the detection of smokeless powder organic additives (in their pre-detonation condition), namely the stabiliser diphenylamine and its derivatives 2-nitrodiphenylamine and 4-nitrodiphenylamine, and the additives (used both as stabilisers and plasticisers) methyl centralite and ethyl centralite, by means of swab sampling followed by thermal desorption and direct injection soft chemical ionisation-mass spectrometry. Investigations on the product ions resulting from the reactions of the reagent ions H 3 O + and O 2 + with additives as a function of reduced electric field are reported. The method was comprehensively evaluated in terms of linearity, sensitivity and precision. For H 3 O + , the limits of detection (LoD) are in the range of 41–88 pg of additive, for which the accuracy varied between 1.5 and 3.2%, precision varied between 3.7 and 7.3% and linearity showed R 2 ≥ 0.9991. For O 2 + , LoD are in the range of 72 to 1.4 ng, with an accuracy of between 2.8 and 4.9% and a precision between 4.5 and 8.6% and R 2 ≥ 0.9914. The validated methodology was applied to the analysis of commercial pre-blast gun powders from different manufacturers. [Figure not available: see fulltext.].

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