Skip to main content
Log in

Optimization of ultraviolet Raman spectroscopy for trace explosive checkpoint screening

  • Paper in Forefront
  • Published:
Analytical and Bioanalytical Chemistry Aims and scope Submit manuscript

Abstract

Raman spectroscopy has long been considered a gold standard for optically based chemical identification, but has not been adopted in non-laboratory operational settings due to limited sensitivity and slow acquisition times. Ultraviolet (UV) Raman spectroscopy has the potential to address these challenges through the reduction of fluorescence from background materials and increased Raman scattering due to the shorter wavelength (relative to visible or near-infrared excitation) and resonant enhancement effects. However, the benefits of UV Raman must be evaluated against specific operational situations: the actual realized fluorescence reduction and Raman enhancement depend on the specific target materials, target morphology, and operational constraints. In this paper, the wavelength trade-space in UV Raman spectroscopy is evaluated for one specific application: checkpoint screening for trace explosive residues. The optimal UV wavelength is evaluated at 244, 266, and 355 nm for realistic trace explosive and explosive-related compound (ERC) residues on common checkpoint materials: we perform semi-empirical analysis that includes the UV penetration depth of common explosive and ERCs, realistic explosive and ERC residue particle sizes, and the fluorescence signal of common checkpoint materials. We find that while generally lower UV wavelength provides superior performance, the benefits may be significantly reduced depending on the specific explosive and substrate. Further, logistical requirements (size, weight, power, and cost) likely limit the adoption of optimal wavelengths.

Graphical abstract

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Pellegrino PM, Holthoff EL, Farrell ME. Laser based optical detection of explosives. 1st ed. Boca Raton: Taylor & Francis Group; 2015. 338 p.

    Book  Google Scholar 

  2. National Research Council of the National Academies, Existing and potential standoff explosives detection techniques, 1st, The National Academies Press, Washington, DC, 2004. 138 p.

  3. Wallin S., Pettersson A., Östmark H., and Hobro A. Laser-based standoff detection of explosives: a critical review. Anal Bioanal Chem 2009. 395:259–274. Available from https://doi.org/10.1007/s00216-009-2844-3

  4. Moore DS. Instrumentation for trace detection of high explosives. Rev Sci Instrum 2004. 75: 2499–2512. Available from https://doi.org/10.1063/1.1771493.

  5. Brown KE, Greenfield MT, McGrane SD, Moore DS. Advances in explosives analysis – part II: photon and neutron methods. Anal Bioanal Chem 2016. 408: 49–65. Available from https://doi.org/10.1007/s00216-015-9043-1.

  6. Elbasuney S,El-Sherif AF. Complete spectroscopic picture of concealed explosives: laser induced Raman versus infrared. Trends Anal Chem 2016. 85: 34–41. Available from https://doi.org/10.1016/j.trac.2016.04.023.

  7. López-López M, García-Ruiz C. Infrared and Raman spectroscopy techniques applied to identification of explosives. Trends Anal Chem. 2014;54:36–44. https://doi.org/10.1016/j.trac.2013.10.011.

    Article  CAS  Google Scholar 

  8. Gares KL, Hufziger KT, Bykov SV, and Asher SA. Review of explosive detection methodologies and the emergence of standoff deep UV resonance Raman. J Raman Spectrosc 2016. 47: 124–141. Available from https://doi.org/10.1002/jrs.4868.

  9. Tuschel DD, Mikhonin AV, Lemoff BE, Asher SA. Deep ultraviolet resonance Raman excitation enables explosives detection. Appl Spectrosc. 2010;64:425–32. Available from https://www.osapublishing.org/as/abstract.cfm?URI=as-64-4-425. https://doi.org/10.1366/000370210791114194. Last accessed on May 15, 2020

  10. Wen P, Amin M, Herzog WD, Kunz RR, Key challenges and prospects for optical standoff trace detection of explosives 2018. 100: 136–144. Available from https://doi.org/10.1016/j.trac.2017.12.014.

  11. Asher SA. UV resonance Raman spectroscopy for analytical, physical, and biophysical chemistry. Part 1. Anal Chem 1993. 65: 59A-66A. Available from https://doi.org/10.1021/ac00050a001.

  12. Emmons ED, Tripathi A, Guicheteau JA, Fountain AW III, Christesen SD. Ultraviolet resonance Raman spectroscopy of explosives in solution and the solid state. J Phys Chem A 2013. 117: 4158–4166. Available from https://doi.org/10.1021/jp402585u.

  13. Sands HS, Hayward IP, Kirkbride TE, Bennett R, Lacey RJ, Batchelder DN. UV-excited resonance Raman spectroscopy of narcotics and explosives. J Forensics Sci. 1998;43:509–13. Available from https://compass.astm.org/DIGITAL_LIBRARY/JOURNALS/JFS/PAGES/JFS16178J.htm. https://doi.org/10.1520/JFS16178J. Last accessed on May 15, 2020

  14. Gares KL, Bykov SV, Asher SA. Solution and solid trinitrotoluene (TNT) photochemistry: persistence of TNT-like ultraviolet (UV) resonance Raman bands. Appl Spectrosc 2014. 68: 49–56. Available from https://doi.org/10.1366/13-07190.

  15. Ghosh M, Wang L, Asher SA. Deep-ultraviolet resonance Raman excitation profiles of NH4NO3, PETN, TNT, HMX, and RDX. Appl Spectrosc 2012. 66: 1013–1021. Available from https://doi.org/10.1366/12-06626.

  16. Yellampalle B, Lemoff BE. Raman albedo and deep-UV resonance Raman signatures of explosives. SPIE Proc. V.8734, Active and Passive Signatures IV, .87340G. (2013). Available from https://www.spiedigitallibrary.org/conference-proceedings-of-spie/8734/87340G/Raman-albedo-and-deep-UV-resonance-Raman-signatures-of-explosives/10.1117/12.2015951. https://doi.org/10.1117/12.2015951. Last accessed on May 15, 2020

  17. Aggarwal, RL, Di Cecca S, Farrar LW, Shabshelowitz A, Jeys TH. Sensitive detection and identification of isovanillin aerosol particles at the pg/cm3 mass concentration level using Raman spectroscopy. Aerosol Sci Technol 2015. 49: 753–756. Available from https://doi.org/10.1080/02786826.2015.1065955.

  18. Kunz RR, Gregory KE, Aernecke MJ, Clark ML, Ostrinskaya A, Fountain, AW III. Fate dynamics of environmentally exposed explosive traces. J Phys Chem A 2012. 116: 3611–3624. Available from https://doi.org/10.1021/jp211260t.

  19. Verkouteren JR, Particle characteristics of trace high explosives: RDX and PETN. J Forensics Sci 2007. 52: 335–340. Available from https://doi.org/10.1111/j.1556-4029.2006.00354.x.

  20. Acosta-Maeda TE, Misra AK, Porter JN, Bates DE, Sharma SK, Remote Raman efficiencies and cross-sections of organic and inorganic chemicals. Appl Spectrosc 2016. 71: 1025–1038. Available from https://doi.org/10.1177/0003702816668531. Last accessed on May 15, 2020

  21. Guenther BD, Snapshot Raman spectral imager. Applied Quantum technologies, Durham, NC, Contract No. W911NF-09-C-0153 March 31, 2010. Available from https://apps.dtic.mil/dtic/tr/fulltext/u2/a522778.pdf.

  22. Beegle LW. Explosives detection and analysis by fusing deep-ultraviolet native fluorescence and resonance Raman spectroscopy. Laser-based optical detection of explosives: Taylor & Francis Ltd; 2015. p. 736.

  23. Asher SA, Johnson CR. Raman-spectroscopy of coal liquid shows that fluorescence interference is minimized with ultraviolet excitation. Science. 1984;225:311–3. Available from https://science.sciencemag.org/content/225/4659/311. https://doi.org/10.1126/science.6740313.

    Article  CAS  PubMed  Google Scholar 

  24. Gaft M, Nagli L, UV gated Raman spectroscopy for standoff detection of explosives, Opt Mater 2008. 30: 1738–1746. Available from https://doi.org/10.1016/j.optmat.2007.11.013.

  25. Matousek P, Towrie M, Stanley A, Parker AW, Efficient rejection of fluorescence from Raman spectra using picosecond Kerr gating, Appl Spectrosc 1993. 53: 1485–1489. Available from https://doi.org/10.1366/0003702991945993.

  26. Emmons, ED, Guicheteau JA, Fountain AW III, Christesen SD. Comparison of visible and near-infrared Raman cross-sections of explosives in solution and in the solid state. Appl Spectrosc 2012. 66: 636–643. Available from https://doi.org/10.1366/11-06549.

Download references

Funding

This work was financially supported by the Science and Technology Directorate of the Department of Homeland Security through Interagency Agreement 70RSAT18KPM000080 under Air Force contract no. FA8702-15-D-0001.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Roderick R. Kunz.

Ethics declarations

Conflict of interest

The authors declare that they have no conflicts of interest.

Research involving human and animal rights

This work did not use human subjects or animals in any of the described research.

Disclaimer

Opinions, interpretations, conclusions, and recommendations are those of the authors and are not necessarily endorsed by the United States Government.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

ESM 1

(PDF 444 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Amin, M., Wen, P., Herzog, W.D. et al. Optimization of ultraviolet Raman spectroscopy for trace explosive checkpoint screening. Anal Bioanal Chem 412, 4495–4504 (2020). https://doi.org/10.1007/s00216-020-02725-2

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00216-020-02725-2

Keywords

Navigation