Accuracies and detection limits of major, minor, and trace element quantification in rocks by portable laser-induced breakdown spectroscopy

2020 ◽  
Vol 171 ◽  
pp. 105946 ◽  
Author(s):  
Cai R. Ytsma ◽  
Christine A. Knudson ◽  
M. Darby Dyar ◽  
Amy C. McAdam ◽  
Danielle D. Michaud ◽  
...  
1998 ◽  
Vol 52 (3) ◽  
pp. 438-443 ◽  
Author(s):  
Leonard M. Berman ◽  
Paul J. Wolf

Spectrochemical analyses of aqueous solutions containing nickel or the chlorinated hydrocarbons (CHCs) C2Cl4, CCl4, CHCl3, and C2HCl3 were performed with the use of laser-induced breakdown spectroscopy. A Nd:YAG laser operating at 60 mJ/pulse was focused onto the surface of the liquid. Elemental line intensities were monitored in the laser-produced plume as a function of analyte concentration to determine detection limits. The limits of detection for nickel in water were 36.4 ± 5.4 mgAL and 18.0 ± 3.8 mg/L for laser irradiation at 1.06 μm and 355 nm, respectively. Ablation of pure CHCs at 355 nm produced extremely intense plasma emissions that primarily consisted of spectroscopic features attributed to CN, C3, H, N, and Cl. The spectra were structurally identical for all the CHCs except for differences in the intensities of various emission lines. With the use of emission from neutral atomic chlorine as an identifier for CHC contamination of water, no detectable traces of these elements were observed in saturated aqueous solutions. The detection limits for the CHCs were well above the saturation limits of CHC in water.


2012 ◽  
Vol 79 (3) ◽  
pp. 471-476 ◽  
Author(s):  
S. S. Golik ◽  
O. A. Bukin ◽  
A. A. Il’in ◽  
E. B. Sokolova ◽  
A. V. Kolesnikov ◽  
...  

2006 ◽  
Vol 385 (2) ◽  
pp. 316-325 ◽  
Author(s):  
Marwa A. Ismail ◽  
Gabriele Cristoforetti ◽  
Stefano Legnaioli ◽  
Lorenzo Pardini ◽  
Vincenzo Palleschi ◽  
...  

2005 ◽  
Vol 59 (9) ◽  
pp. 1082-1097 ◽  
Author(s):  
Karen Y. Yamamoto ◽  
David A. Cremers ◽  
Leeann E. Foster ◽  
Mathew P. Davies ◽  
Ronny D. Harris

Laser-induced breakdown spectroscopy (LIBS) measurements are typically carried out using pulses (<20 ns, >50 mJ) from a flash-lamp-pumped electro-optically Q-switched Nd:YAG laser (EO-laser) or excimer laser. Here we report LIBS analyses of solids using an acousto-optically Q-switched Nd:YAG laser (AO-laser) producing 150 ns pulses of lower energy (10 mJ) at repetition rates up to 6 kHz. The high repetition rate allows increased spatial or depth sampling over a given time period compared to the EO-laser. Results of AO-laser based LIBS analysis of (1) steels, (2) soils, and (3) surface stains and dusts are described. Detection limits for Cr, Cu, Mn, Ni, and Si in steel ranged from 0.11 to 0.24% using a commercial polychromator-based detection system with limits 4–30 times lower achieved using a laboratory-based detection system. The minimum detectable masses of Ba, Cr, Mn, and Sr on a metal surface were estimated with 1.2 pg/shot achieved for Sr. Detection limits for Ba and Sr in soil were 296 and 52 ppm, respectively. The temperatures, spectra, and emission decay curves from plasmas generated by the AO- and EO-lasers are compared and some characteristics of particles ablated by the AO-laser are described.


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