Time-integrated laser-induced plasma spectroscopy in the vacuum ultraviolet for the quantitative elemental characterization of steel alloys

Citation
Ma. Khater et al., Time-integrated laser-induced plasma spectroscopy in the vacuum ultraviolet for the quantitative elemental characterization of steel alloys, J PHYS D, 33(18), 2000, pp. 2252-2262
Citations number
70
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
JOURNAL OF PHYSICS D-APPLIED PHYSICS
ISSN journal
00223727 → ACNP
Volume
33
Issue
18
Year of publication
2000
Pages
2252 - 2262
Database
ISI
SICI code
0022-3727(20000921)33:18<2252:TLPSIT>2.0.ZU;2-V
Abstract
This paper demonstrates that time-integrated space-resolved laser-induced p lasma spectroscopy (TISR-LIPS) is a useful technique in the vacuum ultravio let (VUV) for the quantitative determination of the carbon content in steel s. The standard reference samples used were carbon-iron alloys containing a relatively wide concentration range of carbon (0.041-1.32%). in the experi ments the output of a Q-switched Nd:YAG (1064 nm) laser, with approximately a 1 J maximum output pulse energy and approximately a 12 ns temporal pulse width, was focused onto the surface of each sample (under vacuum) in order to produce the emitting plasma. A fore-slit mounted in the target chamber allowed spatially-resolved spectral measurements in the axial direction of the plasma and provided emission lines that were almost free of the backgro und continuum. A 1 m normal incidence vacuum spectrometer, equipped with a 1200 grooves mm(-1) concave grating and a micro-channel plate/photodiode ar ray detector combination, was used as the detection system. A particularly interesting feature of this work is the demonstration that VUV spectroscopy allows ionic lines to be used and linear calibration curves were obtained for the five carbon spectral Lines (from C+ and C2+) under investigation. T he limits of detection for all lines were determined: the lowest detection limit (87 +/- 10 ppm) was obtained from the C2+ 97.70 nm line, which compar es favourably with the only available value in the literature of 100 ppm.