Review: Applications of single-shot laser-induced breakdown spectroscopy

2010 ◽  
Vol 65 (3) ◽  
pp. 185-191 ◽  
Author(s):  
Anna P.M. Michel
2019 ◽  
Vol 74 (1) ◽  
pp. 42-54 ◽  
Author(s):  
Daniel Diaz ◽  
Alejandro Molina ◽  
David W. Hahn

Laser-induced breakdown spectroscopy (LIBS) and principal component analysis (PCA) were applied to the classification of LIBS spectra from gold ores prepared as pressed pellets from pulverized bulk samples. For each sample, 5000 single-shot LIBS spectra were obtained. Although the gold concentrations in the samples were as high as 7.7 µg/g, Au emission lines were not observed in most single-shot LIBS spectra, rendering the application of the usual ensemble-averaging approach for spectral processing to be infeasible. Instead, a PCA approach was utilized to analyze the collection of single-shot LIBS spectra. Two spectral ranges of 21 nm and 0.15 nm wide were considered, and LIBS variables (i.e., wavelengths) reduced to no more than three principal components. Single-shot spectra containing Au emission lines (positive spectra) were discriminated by PCA from those without the spectral feature (negative spectra) in a spectral range of less than 1 nm wide around the Au(I) 267.59 nm emission line. Assuming a discrete gold distribution at very low concentration, LIBS sampling of gold particles seemed unlikely; therefore, positive spectra were considered as data outliers. Detection of data outliers was possible using two PCA statistical parameters, i.e., sample residual and Mahalanobis distance. Results from such a classification were compared with a standard database created with positive spectra identified with a filtering algorithm that rejected spectra with an Au intensity below the smallest detectable analytical LIBS signal (i.e., below the LIBS limit of detection). The PCA approach successfully identified 100% of the data outliers when compared with the standard database. False identifications in the multivariate approach were attributed to variations in shot-to-shot intensity and the presence of interfering emission lines.


1999 ◽  
Vol 71 (23) ◽  
pp. 5447-5449 ◽  
Author(s):  
I. B. Gornushkin ◽  
B. W. Smith ◽  
G. E. Potts ◽  
N. Omenetto ◽  
J. D. Winefordner

2020 ◽  
Vol 74 (3) ◽  
pp. 340-346 ◽  
Author(s):  
Mark Gragston ◽  
Paul Hsu ◽  
Anil Patnaik ◽  
Zhili Zhang ◽  
Sukesh Roy

Time-gated picosecond laser-induced breakdown spectroscopy (ps-LIBS) for the determination of local equivalence ratios in atmospheric-pressure adiabatic methane–air flames is demonstrated. Traditional LIBS for equivalence-ratio measurements employ nanosecond (ns)-laser pulses, which generate excessive amounts of continuum, reducing measurement accuracy and precision. Shorter pulse durations reduce the continuum emission by limiting avalanche ionization. Furthermore, by contrast the use of femtosecond lasers, plasma emission using picosecond-laser excitation has a high signal-to-noise ratio (S/N), allowing single-shot measurements suitable for equivalence-ratio determination in turbulent reacting flows. We carried out an analysis of the dependence of the plasma emission ratio Hα (656 nm)/NII (568 nm) on laser energy and time-delay for optimization of S/N and minimization of measurement uncertainties in the equivalence ratios. Our finding shows that higher laser energy and shorter time delay reduces measurement uncertainty while maintaining high S/N. In addition to atmospheric-pressure flame studies, we also examine the stability of the ps-LIBS signal in a high-pressure nitrogen cell. The results indicate that the plasma emission and spatial position could be stable, shot-to-shot, at elevated pressure (up to 40 bar) using a lower excitation energy. Our work shows the potential of using ps-duration pulses to improve LIBS-based equivalence-ratio measurements, both in atmospheric and high-pressure combustion environments.


2019 ◽  
Vol 34 (12) ◽  
pp. 2411-2419 ◽  
Author(s):  
Erik Képeš ◽  
Pavel Pořízka ◽  
Jozef Kaiser

The acquisition of single-shot spectra combined with bootstrapping provides superior spectral quality in laser-induced breakdown spectroscopy.


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