Effect of Sampling Geometry on Elemental Emissions in Laser-Induced Breakdown Spectroscopy

1996 ◽  
Vol 50 (12) ◽  
pp. 1483-1499 ◽  
Author(s):  
Rosalie A. Multari ◽  
Leeann E. Foster ◽  
David A. Cremers ◽  
Monty J. Ferris

In laser-induced breakdown spectroscopy (LIBS), a focused laser pulse is used to ablate material from a surface and form a laser plasma that excites the vaporized material. Geometric factors, such as the distance between the sample and the focusing lens and the method of collecting the plasma light, can greatly influence the analytical results. To obtain the best quantitative results, one must consider this geometry. Here we report the results of an investigation of the effect of sampling geometry on LIBS measurements. Diagnostics include time-resolved spectroscopy and temporally and spectrally resolved imaging using an acousto-optic tunable filter (AOTF). Parameters investigated include the type of lens (cylindrical or spherical) used to focus the laser pulse onto the sample, the focal length of the lens (75 or 150 mm), the lens-to-sample distance (LTSD), the angle-of-incidence of the laser pulse onto the sample, and the method used to collect the plasma light (lens or fiber-optic bundle). From these studies, it was found that atomic emission intensities, plasma temperature, and mass of ablated material depend strongly on the LTSD for both types of lenses. For laser pulse energies above the breakdown threshold for air, these quantities exhibit symmetric behavior about an LTSD approximately equal to the back focal length for cylindrical lenses and asymmetric behavior for spherical lenses. For pulse energies below the air breakdown threshold, results obtained for both lenses display symmetric behavior. Detection limits and measurement precision for the elements Be, Cr, Cu, Mn, Pb, and Sr, determined with the use of 14 certified reference soils and stream sediments, were found to be independent of the lens used. Time-resolved images of the laser plasma show that at times >5 μs after plasma formation a cloud of emitting atoms extends significantly beyond the centrally located, visibly white, intense plasma core present at early times (<0.3 μs). It was determined that, by collecting light from the edges of the emitting cloud, one can record spectra using an ungated detector (no time resolution) that resemble closely the spectra obtained from a gated detector providing time-resolved detection. This result has implications in the development of less expensive LIBS detection systems.

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Emanuela Grifoni ◽  
Stefano Legnaioli ◽  
Marco Lezzerini ◽  
Giulia Lorenzetti ◽  
Stefano Pagnotta ◽  
...  

Laser-induced breakdown spectroscopy (LIBS) data are characterized by a strong dependence on the acquisition time after the onset of the laser plasma. However, time-resolved broadband spectrometers are expensive and often not suitable for being used in portable LIBS instruments. In this paper we will show how the analysis of a series of LIBS spectra, taken at different delays after the laser pulse, allows the recovery of time-resolved spectral information. The comparison of such spectra is presented for the analysis of an aluminium alloy. The plasma parameters (electron temperature and number density) are evaluated, starting from the time-integrated and time-resolved spectra, respectively. The results are compared and discussed.


2005 ◽  
Vol 60 (11) ◽  
pp. 1392-1401 ◽  
Author(s):  
P.A. Benedetti ◽  
G. Cristoforetti ◽  
S. Legnaioli ◽  
V. Palleschi ◽  
L. Pardini ◽  
...  

2020 ◽  
Vol 92 (2) ◽  
pp. 20701
Author(s):  
Bo Li ◽  
Xiaofeng Li ◽  
Zhifeng Zhu ◽  
Qiang Gao

Laser-induced breakdown spectroscopy (LIBS) is a powerful technique for quantitative diagnostics of gases. The spatial resolution of LIBS, however, is limited by the volume of plasma. Here femtosecond-nanosecond dual-pulsed LIBS was demonstrated. Using this method, the breakdown threshold was reduced by 80%, and decay of continuous radiation was shortened. In addition, the volume of the plasma was shrunk by 85% and hence, the spatial resolution of LIBS was significantly improved.


1992 ◽  
Vol 46 (9) ◽  
pp. 1382-1387 ◽  
Author(s):  
J. A. Aguilera ◽  
C. Aragón ◽  
J. Campos

Laser-induced breakdown spectroscopy has been used to determine carbon content in steel. The plasma was formed by focusing a Nd:YAG laser on the sample surface. With the use of time-resolved spectroscopy and generation of the plasma in nitrogen atmosphere, a precision of 1.6% and a detection limit of 65 ppm have been obtained. These values are similar to those of other accurate conventional techniques. Matrix effects for the studied steels are reduced to a small slope difference between the calibration curves for stainless and nonstainless steels.


2007 ◽  
Vol 62 (12) ◽  
pp. 1329-1334 ◽  
Author(s):  
Matthieu Baudelet ◽  
Myriam Boueri ◽  
Jin Yu ◽  
Samuel S. Mao ◽  
Vincent Piscitelli ◽  
...  

AIP Advances ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 065214 ◽  
Author(s):  
Kaimin Guo ◽  
Anmin Chen ◽  
Wanpeng Xu ◽  
Dan Zhang ◽  
Mingxing Jin

2008 ◽  
Vol 62 (10) ◽  
pp. 1137-1143 ◽  
Author(s):  
Dário Santos ◽  
Ricardo Elgul Samad ◽  
Lílian Cristina Trevizan ◽  
Anderson Zanardi de Freitas ◽  
Nilson Dias Vieira ◽  
...  

The aim of this work was to evaluate the performance of femtosecond laser-induced breakdown spectroscopy (fs-LIBS) for the determination of elements in animal tissues. Sample pellets were prepared from certified reference materials, such as liver, kidney, muscle, hepatopancreas, and oyster, after cryogenic grinding assisted homogenization. Individual samples were placed in a two-axis computer-controlled translation stage that moved in the plane orthogonal to a beam originating from a Ti:Sapphire chirped-pulse amplification (CPA) laser system operating at 800 nm and producing a train of 840 μJ and 40 fs pulses at 90 Hz. The plasma emission was coupled into the optical fiber of a high-resolution intensified charge-coupled device (ICCD)–echelle spectrometer. Time-resolved characteristics of the laser-produced plasmas showed that the best results were obtained with delay times between 80 and 120 ns. Data obtained indicate both that it is a matrix-independent sampling process and that fs-LIBS can be used for the determination of Ca, Cu, Fe, K, Mg, Na, and P, but efforts must be made to obtain more appropriate detection limits for Al, Sr, and Zn.


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