Physics:Laser-induced breakdown spectroscopy

From HandWiki
Short description: Type of atomic emission spectroscopy
Schematic of a LIBS system – Courtesy of US Army Research Laboratory

Laser-induced breakdown spectroscopy (LIBS) is a type of atomic emission spectroscopy which uses a highly energetic laser pulse as the excitation source.[1][2] The laser is focused to form a plasma, which atomizes and excites samples. The formation of the plasma only begins when the focused laser achieves a certain threshold for optical breakdown, which generally depends on the environment and the target material.[3]

2000s developments

From 2000 to 2010, the U.S. Army Research Laboratory (ARL) researched potential extensions to LIBS technology, which focused on hazardous material detection.[4][5] Applications investigated at ARL included the standoff detection of explosive residues and other hazardous materials, plastic landmine discrimination, and material characterization of various metal alloys and polymers. Results presented by ARL suggest that LIBS may be able to discriminate between energetic and non-energetic materials.[6]

Research

Broadband high-resolution spectrometers were developed in 2000 and commercialized in 2003. Designed for material analysis, the spectrometer allowed the LIBS system to be sensitive to chemical elements in low concentration.[7]

ARL LIBS applications studied from 2000 to 2010 included:[5]

  • Tested for detection of Halon alternative agents
  • Tested a field-portable LIBS system for the detection of lead in soil and paint
  • Studied the spectral emission of aluminum and aluminum oxides from bulk aluminum in different bath gases
  • Performed kinetic modeling of LIBS plumes
  • Demonstrated the detection and discrimination of geological materials, plastic landmines, explosives, and chemical and biological warfare agent surrogates

ARL LIBS prototypes studied during this period included:[5]

  • Laboratory LIBS setup
  • Commercial LIBS system
  • Man-portable LIBS device
  • Standoff LIBS system developed for 100+ m detection and discriminate on of explosive residues.

2010s developments

LIBS is one of several analytical techniques that can be deployed in the field as opposed to pure laboratory techniques e.g. spark OES. (As of 2015), recent research on LIBS focuses on compact and (man-)portable systems. Some industrial applications of LIBS include the detection of material mix-ups,[8] analysis of inclusions in steel, analysis of slags in secondary metallurgy,[9] analysis of combustion processes,[10] and high-speed identification of scrap pieces for material-specific recycling tasks. Armed with data analysis techniques, this technique is being extended to pharmaceutical samples.[11][12]

LIBS using short laser pulses

Following multiphoton or tunnel ionization the electron is being accelerated by inverse Bremsstrahlung and can collide with the nearby molecules and generate new electrons through collisions. If the pulse duration is long, the newly ionized electrons can be accelerated and eventually avalanche or cascade ionization follows. Once the density of the electrons reaches a critical value, breakdown occurs and high density plasma is created which has no memory of the laser pulse. So, the criterion for the shortness of a pulse in dense media is as follows: A pulse interacting with a dense matter is considered to be short if during the interaction the threshold for the avalanche ionization is not reached. At the first glance this definition may appear to be too limiting. Fortunately, due to the delicately balanced behavior of the pulses in dense media, the threshold cannot be reached easily.[citation needed] The phenomenon responsible for the balance is the intensity clamping[13] through the onset of filamentation process during the propagation of strong laser pulses in dense media.

A potentially important development to LIBS involves the use of a short laser pulse as a spectroscopic source.[14] In this method, a plasma column is created as a result of focusing ultrafast laser pulses in a gas. The self-luminous plasma is far superior in terms of low level of continuum and also smaller line broadening. This is attributed to the lower density of the plasma in the case of short laser pulses due to the defocusing effects which limits the intensity of the pulse in the interaction region and thus prevents further multiphoton/tunnel ionization of the gas.[15][16]

Line intensity

For an optically thin plasma composed of a single, neutral atomic species in local thermal equilibrium (LTE), the density of photons emitted by a transition from level i to level j is[17]

[math]\displaystyle{ I_{ij}(\lambda)=\frac{1}{4\pi} n_0 A_{ij}\frac{ g_i \exp^{-E_i/k_B T}}{U(T)} I(\lambda) }[/math]

where :

  • [math]\displaystyle{ I_{ij} }[/math] is the emission rate density of photons (in m−3 sr−1 s−1)
  • [math]\displaystyle{ n_0 }[/math] is the number of neutral atoms in the plasma (in m−3)
  • [math]\displaystyle{ A_{ij} }[/math] is the transition probability between level i and level j (in s−1)
  • [math]\displaystyle{ g_i }[/math] is the degeneracy of the upper level i (2J+1)
  • [math]\displaystyle{ U(T) }[/math] is the partition function (unitless)
  • [math]\displaystyle{ E_i }[/math] is the energy level of the upper level i (in eV)
  • [math]\displaystyle{ k_B }[/math] is the Boltzmann constant (in eV/K)
  • [math]\displaystyle{ T }[/math] is the temperature (in K)
  • [math]\displaystyle{ I(\lambda) }[/math] is the line profile such that [math]\displaystyle{ \int_{-\infty}^{\infty}I(\lambda)d\lambda = 1 }[/math]
  • [math]\displaystyle{ \lambda }[/math] is the wavelength (in nm)

The partition function [math]\displaystyle{ U(T) }[/math] is the statistical occupation fraction of every level [math]\displaystyle{ k }[/math] of the atomic species :

[math]\displaystyle{ U(T) = \sum_j g_j \exp^{-E_j/k_B T} }[/math]

LIBS for food analysis

Recently, LIBS has been investigated as a fast, micro-destructive food analysis tool. It is considered a potential analytical tool for qualitative and quantitative chemical analysis, making it suitable as a PAT (Process Analytical Technology) or portable tool. Milk, bakery products, tea, vegetable oils, water, cereals, flour, potatoes, palm date and different types of meat have been analyzed using LIBS.[18] Few studies have shown its potential as an adulteration detection tool for certain foods.[19][20] LIBS has also been evaluated as a promising elemental imaging technique in meat.[21]

In 2019, researchers of the University of York and of the Liverpool John Moores University employed LIBS for studying 12 European oysters (Ostrea edulis, Linnaeus, 1758) from the Late Mesolithic shell midden at Conors Island (Republic of Ireland). The results highlighted the applicability of LIBS to determine prehistoric seasonality practices as well as biological age and growth at an improved rate and reduced cost than was previously achievable.[22][23]

See also

References

  1. ↑ Radziemski, Leon J.; Cremers, David A. (2006). Handbook of laser-induced breakdown spectroscopy. New York: John Wiley. ISBN 0-470-09299-8. 
  2. ↑ Schechter, Israel; Miziolek, Andrzej W.; Vincenzo Palleschi (2006). Laser-induced breakdown spectroscopy (LIBS): fundamentals and applications. Cambridge, UK: Cambridge University Press. ISBN 0-521-85274-9. 
  3. ↑ J. P. Singh and S. N. Thakur, Laser-Induced Breakdown Spectroscopy, 1st ed.. (Elsevier, 2007).
  4. ↑ Munson, Jennifer L. Gottfried Frank C. De Lucia Jr. Andrzej W. Miziolek Chase A. (June 2009). "Current Status of Standoff LIBS Security Applications at the United States Army Research Laboratory" (in en). Spectroscopy. Spectroscopy-06-01-2009 24 (6). http://www.spectroscopyonline.com/current-status-standoff-libs-security-applications-united-states-army-research-laboratory-0. Retrieved 2018-08-27. 
  5. ↑ 5.0 5.1 5.2 Gottfried, Jennifer L.; De Lucia, Frank C. Jr. (2010). Laser-Induced Breakdown Spectroscopy: Capabilities and Applications. doi:10.21236/ada528756. 
  6. ↑ "Detection of Energetic Materials and Explosive Residues With Laser-Induced Breakdown Spectroscopy: I. Laboratory Measurements". https://apps.dtic.mil/dtic/tr/fulltext/u2/a472707.pdf. 
  7. ↑ "U.S. Army Researchers Explore Laser Detection Techniques | Quality Digest" (in en). https://www.qualitydigest.com/inside/twitter-ed/us-army-researchers-explore-laser-detection-techniques.html. 
  8. ↑ Noll, Reinhard; Bette, Holger; Brysch, Adriane; Kraushaar, Marc; Mönch, Ingo; Peter, Laszlo; Sturm, Volker (2001). "Laser-induced breakdown spectrometry — applications for production control and quality assurance in the steel industry". Spectrochimica Acta Part B: Atomic Spectroscopy 56 (6): 637–649. doi:10.1016/s0584-8547(01)00214-2. Bibcode: 2001AcSpe..56..637N. 
  9. ↑ Sanghapi, Hervé K.; Ayyalasomayajula, Krishna K.; Yueh, Fang Y.; Singh, Jagdish P.; McIntyre, Dustin L.; Jain, Jinesh C.; Nakano, Jinichiro (2016). "Analysis of slags using laser-induced breakdown spectroscopy". Spectrochimica Acta Part B: Atomic Spectroscopy 115: 40–45. doi:10.1016/j.sab.2015.10.009. Bibcode: 2016AcSpe.115...40S. 
  10. ↑ Hsu, Paul S.; Gragston, Mark; Wu, Yue; Zhang, Zhili; Patnaik, Anil K.; Kiefer, Johannes; Roy, Sukesh; Gord, James R. (2016). "Sensitivity, stability, and precision of quantitative Ns-LIBS-based fuel-air-ratio measurements for methane-air flames at 1–11 bar". Applied Optics 55 (28): 8042–8048. doi:10.1364/ao.55.008042. PMID 27828047. Bibcode: 2016ApOpt..55.8042H. 
  11. ↑ St-Onge, L.; Kwong, E.; Sabsabi, M.; Vadas, E.B (2002). "Quantitative analysis of pharmaceutical products by laser-induced breakdown spectroscopy". Spectrochimica Acta Part B: Atomic Spectroscopy 57 (7): 1131–1140. doi:10.1016/s0584-8547(02)00062-9. Bibcode: 2002AcSpe..57.1131S. 
  12. ↑ Myakalwar, Ashwin Kumar; Sreedhar, S.; Barman, Ishan; Dingari, Narahara Chari; Venugopal Rao, S.; Prem Kiran, P.; Tewari, Surya P.; Manoj Kumar, G. (2011). "Laser-induced breakdown spectroscopy-based investigation and classification of pharmaceutical tablets using multivariate chemometric analysis". Talanta 87: 53–59. doi:10.1016/j.talanta.2011.09.040. PMID 22099648. 
  13. ↑ Xu, Shengqi; Sun, Xiaodong; Zeng, Bin; Chu, Wei; Zhao, Jiayu; Liu, Weiwei; Cheng, Ya; Xu, Zhizhan et al. (2012). "Simple method of measuring laser peak intensity inside femtosecond laser filament in air". Optics Express 20 (1): 299–307. doi:10.1364/oe.20.000299. PMID 22274353. Bibcode: 2012OExpr..20..299X. 
  14. ↑ A. Talebpour et al., Spectroscopy of the Gases Interactingwith Intense Femtosecond Laser Pulses, 2001, Laser Physics, 11:68–76
  15. ↑ Talebpour, A.; Abdel-Fattah, M.; Chin, S.L (2000). "Focusing limits of intense ultrafast laser pulses in a high pressure gas: Road to new spectroscopic source". Optics Communications 183 (5–6): 479–484. doi:10.1016/s0030-4018(00)00903-2. Bibcode: 2000OptCo.183..479T. 
  16. ↑ Geints, Yu. E.; Zemlyanov, A. A. (2009). "On the focusing limit of high-power femtosecond laser pulse propagation in air". The European Physical Journal D 55 (3): 745–754. doi:10.1140/epjd/e2009-00260-0. Bibcode: 2009EPJD...55..745G. 
  17. ↑ Reinhard., Noll (2012). Laser-induced breakdown spectroscopy: fundamentals and applications. Springer-Verlag Berlin Heidelberg. ISBN 978-3-642-20667-2. OCLC 773812336. 
  18. ↑ Markiewicz-Keszycka, Maria (2017). "Laser-induced breakdown spectroscopy (LIBS) for food analysis: A review". Trends in Food Science & Technology 65: 80–93. doi:10.1016/j.tifs.2017.05.005. https://arrow.tudublin.ie/cgi/viewcontent.cgi?article=1508&context=schfsehart. 
  19. ↑ Sezer, Banu (2018). "Identification of milk fraud using laser-induced breakdown spectroscopy (LIBS)". International Dairy Journal 81: 1–7. doi:10.1016/j.idairyj.2017.12.005. 
  20. ↑ Dixit, Yash (2017). "Laser induced breakdown spectroscopy for quantification of sodium and potassium in minced beef: a potential technique for detecting beef kidney adulteration". Analytical Methods 9 (22): 3314–3322. doi:10.1039/C7AY00757D. https://arrow.dit.ie/schfsehart/291. 
  21. ↑ Dixit, Yash (2018). "Introduction to laser induced breakdown spectroscopy imaging in food: Salt diffusion in meat". Journal of Food Engineering 216: 120–124. doi:10.1016/j.jfoodeng.2017.08.010. https://arrow.dit.ie/schfsehart/273. 
  22. ↑ Hausmann, N.; Prendergast, A. L.; Lemonis, A.; Zech, J.; Roberts, P.; Siozos, P.; Anglos, D. (2019-03-06). "Extensive elemental mapping unlocks Mg/Ca ratios as climate proxy in seasonal records of Mediterranean limpets" (in en). Scientific Reports 9 (1): 3698. doi:10.1038/s41598-019-39959-9. ISSN 2045-2322. PMID 30842602. Bibcode: 2019NatSR...9.3698H. 
  23. ↑ Hausmann, Niklas; Robson, Harry K.; Hunt, Chris (2019-09-30). "Annual Growth Patterns and Interspecimen Variability in Mg/Ca Records of Archaeological Ostrea edulis (European Oyster) from the Late Mesolithic Site of Conors Island" (in en). Open Quaternary 5 (1): 9. doi:10.5334/oq.59. ISSN 2055-298X. 
  • Lee, Won-Bae; Wu, Jianyong; Lee, Yong-Ill; Sneddon, Joseph (2004). "Recent Applications of Laser-Induced Breakdown Spectrometry: A Review of Material Approaches". Applied Spectroscopy Reviews 39 (1): 27–97. doi:10.1081/ASR-120028868. ISSN 0570-4928. Bibcode: 2004ApSRv..39...27L. 
  • Noll, Reinhard; Bette, Holger; Brysch, Adriane; Kraushaar, Marc; Mönch, Ingo; Peter, Laszlo; Sturm, Volker (2001). "Laser-induced breakdown spectrometry — applications for production control and quality assurance in the steel industry". Spectrochimica Acta Part B: Atomic Spectroscopy 56 (6): 637–649. doi:10.1016/S0584-8547(01)00214-2. ISSN 0584-8547. Bibcode: 2001AcSpe..56..637N. 

Further reading

External links



Retrieved from "https://handwiki.org/wiki/index.php?title=Physics:Laser-induced_breakdown_spectroscopy&oldid=3281782"