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Self-Calibrated Laser-Induced Breakdown Spectroscopy for the Quantitative Elemental Analysis of Suspended Volcanic Ash.
Taleb, Aya; Dell'Aglio, Marcella; Gaudiuso, Rosalba; Mele, Daniela; Dellino, Pierfrancesco; De Giacomo, Alessandro.
Afiliación
  • Taleb A; Department of Chemistry, University of Bari, Bari, Italy.
  • Dell'Aglio M; CNR-IFN (National Research Council-Institute for Photonics and Nanotechnologies), C-O Physics Department, University of Bari, Bari, Italy.
  • Gaudiuso R; Department of Chemistry, University of Bari, Bari, Italy.
  • Mele D; Department of Earth and Geoenvironmental Sciences, University of Bari, Bari, Italy.
  • Dellino P; Department of Earth and Geoenvironmental Sciences, University of Bari, Bari, Italy.
  • De Giacomo A; Department of Chemistry, University of Bari, Bari, Italy.
Appl Spectrosc ; 78(7): 714-726, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38529539
ABSTRACT
Real-time analysis of fine ash in volcanic plumes, which represent magma fragments expelled from the crater during explosive eruptions, is a valuable tool for volcano monitoring and hazard assessment. To obtain the chemical characterization of the juvenile pyroclastic material emitted in volcanic plumes, many analytical techniques can be used. Among them, laser-induced breakdown spectroscopy (LIBS) is the one that can most easily be adapted to advanced applications in extreme environments. In this paper, LIBS experiments based on self-calibrated approaches are used to determine the elemental composition of suspended volcanic ash. To simulate the conditions of dispersed volcanic ash in the atmosphere, different sizes of volcanic ash samples are suspended in the air by laser-induced shockwaves in a dedicated chamber, and a parametric study is carried out to establish the optimal experimental conditions for recording usable plasma emission spectra for each ash size. The quantitative analysis is performed using a self-calibrated analytical method, including calibration-free LIBS, which is based on the calculation of the spectral radiance of a uniform plasma in local thermodynamic equilibrium. The method accounts intrinsically for self-absorption since it modifies the intensity of spectral lines and thus leads to an underestimation of the elemental fraction. An intensity calibration of the spectra based on the measurements of Fe lines intensities was also used in this work to deduce the apparatus response from the spectrum itself and avoid the use of standard calibration lamps. Results demonstrate the potential of real-time measurements of elemental fractions in volcanic ash with good agreement with the literature composition.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Appl Spectrosc Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Appl Spectrosc Año: 2024 Tipo del documento: Article País de afiliación: Italia