An evaluation of a commercial Echelle spectrometer with intensified charge-coupled device detector for materials analysis by laser-induced plasma spectroscopy

Citation
V. Detalle et al., An evaluation of a commercial Echelle spectrometer with intensified charge-coupled device detector for materials analysis by laser-induced plasma spectroscopy, SPECT ACT B, 56(6), 2001, pp. 1011-1025
Citations number
18
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY
ISSN journal
05848547 → ACNP
Volume
56
Issue
6
Year of publication
2001
Pages
1011 - 1025
Database
ISI
SICI code
0584-8547(20010629)56:6<1011:AEOACE>2.0.ZU;2-5
Abstract
In this work we evaluate the performance of a commercial Echelle spectromet er coupled with an intensified charge-coupled device (ICCD) detector for th e analysis of solid samples by laser-induced plasma spectroscopy (LIPS) in air at atmospheric pressure. We compare results obtained in aluminum alloy samples with this system and with a 'conventional' Czerny-Turner spectromet er coupled to an intensified photodiode array (IPDA). We used both systems to generate calibration curves and to determine the detection limit of mino r elements, such as Mg, Cu, Si, etc. Our results indicate that no significa nt differences in terms of analytical figures of merit exist between the Ec helle/ICCD system and a conventional Czerny-Turner spectrometer with IPDA. Moreover, measurements of plasma temperature and electron density using the two assemblies give, in general, very similar results. In the second part of this work, we aim to present a critical view of the Echelle spectrometer for LIPS applications, by drawing up the balance sheet of the advantages a nd limitations of the apparatus. The limitations are either inherent to the dispersion method, or result from the dynamic range of the detector. Moreo ver, the minimum ICCD readout time does not allow a fast data acquisition r ate. On the other hand, the Echelle spectrometer allows complete elemental analysis in a single shot, as spectral lines of major, minor and trace cons tituents, as well as plasma parameters, are measured simultaneously. This e nables a real-time identification of unknown matrices and an improvement in the analytical precision by selecting several lines for the same element. (C) 2001 Elsevier Science B.V. All rights reserved.