Violeta Lazic

A comparison of single and double pulse laser-induced breakdown spectroscopy of aluminum samples

Abstract Single and double pulse laser-induced breakdown spectroscopy (LIBS) was carried out on aluminum samples in air. In the case of double pulse excitation, experiments were conducted by using the same laser source operated at the same wavelength (1064 nm in most cases here presented). A lowering of the second pulse plasma threshold was observed, together with an overall enhancement in line emission for the investigated time delay between the two pulses (40–60 μs). The laser-induced plasma originated by a single and double pulse was investigated near ignition threshold with the aim to study possible dynamical mechanisms in different regimes. Currently available spectroscopic diagnostics of plasma, such as the line broadening and shift due Stark effects, have been used in the characterization in order to retrieve electron densities, while standard temperature measurements were based on Boltzmann plot. Plasma relevant parameters, such as temperature and electron density, have been measured in the plasma decay on a long time scale, and compared with crater shape (diameter and inferred volume). The comparison of double with single pulse laser excitation was carried out while keeping constant the energy per pulse; the influence of laser energy was investigated as well. Results here obtained suggest that use of the double pulse technique could significantly improve the analytical capabilities of LIBS technique in routine laboratory experiments.

Laser-induced breakdown spectroscopy for semi-quantitative and quantitative analyses of artworks—application on multi-layered ceramics and copper based alloys ☆

Abstract In the present work, we report on the analyses of different types of artworks, such as medieval glazed Umbrian pottery and copper based alloys from Roman and modern periods, performed by means of Laser Induced Breakdown Spectroscopy (LIBS). The semi-quantitative analyses on the multi-layered ceramic findings regard glaze, luster and pigment decorations present on the surface. The composition for each decorative layer was determined by estimating the contribution of the ceramic layer beneath the examined one to the whole plasma emission. Two types of ancient luster have been considered: red and gold, while the pigments examined include painted decorations of different blue tonalities. The measured elemental composition of the decorative layers resulted partially correlated with the color of the painted surface, measured by a standard UV-VIS spectrometer. In LIBS analyses of bronze samples, a procedure was developed, which improves data repeatability and extends quantitative measurements to minor elemental constituents. Results of the quantitative analyses gave indications about the manufacturing process of the artwork, its actual degree of conservation and the presence of residual surface decorations.

Quantitative laser induced breakdown spectroscopy analysis of ancient marbles and corrections for the variability of plasma parameters and of ablation rate

White marble samples from ancient quarries have been analyzed by Laser Induced Breakdown Spectroscopy (LIBS) both on the bulk material and surface encrustations. With the aim to achieve quantitative results by LIBS, until now not reported on marble materials, calibration standards with CaCO3 matrices doped with certified soils were realized. Very different emission intensities and plasma parameters were observed on the standards and natural marbles. In order to compare so different spectra, a method for data analysis was developed, which takes into account variability of the ablation rate, plasma temperature and electron density. It was experimentally demonstrated that ablated volume is well correlated to the emission intensity of plasma continuum for a wide range of laser energies. LIBS signal normalization on the adjacent continuum level, together with introduction of correction factors dependent on plasma parameters, allowed the measuring of concentrations both for major and trace elements in marbles. The analytical procedure was validated by comparative SEM-EDX and ICP-OES measurements. Quantitative LIBS analyses were also performed during encrustation removal and could be applied to control laser-cleaning processes. The quantification of metal contents in the encrustations supported the occurrence of sulfates in the outer layers exposed to environmental agents via a catalytic process.

LIBS as a diagnostic tool during the laser cleaning of copper based alloys: experimental results

In spite of difficulties in quantitative LIBS analysis on copper based alloys, the very low invasiveness of the technique strongly sustains attempts to use it with cultural heritage materials, including ancient bronzes. Analytical results obtained with calibration curves and a calibration free model are compared here on a set of ancient roman coins. An attempt is presented to monitor the laser ablation process on bronze coins and artificially aged standards during the cleaning. The double pulse technique showed that LIBS analytical results could benefit from synchronization between the UV laser sources used, respectively, for cleaning (266 nm) and for LIBS analysis (335 nm).

Deep Ablation and Depth Profiling by Laser-Induced Breakdown Spectroscopy (LIBS) Employing Multi-Pulse Laser Excitation: Application to Galvanized Steel

The potential of a multi-pulse (MP) laser excitation scheme for deep stratigraphy of electrolytically galvanized steel using laser-induced breakdown spectrometry (LIBS) has been evaluated. For this purpose, a commercial electro-optically (EO) Q-switched Nd:YAG laser was employed, where by reducing the delay between the Q-switch opening and the flash lamp, a train of pulses (up to 11) separated by approximately 7.40 μs was generated during one lamp flashing. Plasma emission after each individual laser pulse of the MP sequence was detected by a spectrograph equipped with an intensified charge-coupled device (iCCD) detector. With MP excitation, the ablation efficiency was increased tenfold on iron sample and 22.5-fold on zinc material with respect to dual-pulse or single-pulse excitation. The LIBS signal generated by MP excitation shows an analogous enhancement. Although the total energy per shot delivered to samples was only 60 mJ, it was possible using LIBS to measure the sample stratigraphy up to depths of 90 lm on zinc-coated steel sheets. A satisfactory agreement between the Zn thickness determined by the MP-LIBS system and data from the manufacturer has also been obtained.

Quantitative elemental analyses of archaeological materials by laser-induced breakdown spectroscopy (LIBS): an overview

LIBS is one of the most promising techniques for rapid, in-situ elemental analyses of artworks. It does not require sample preparation, it is almost non destructive (micro sampling) and information both about major and trace elements could be obtained simultaneously. LIBS has been used to recognize the elements present in different archaeological materials and has been also proposed for on-line monitoring during the object cleaning by lasers. Quantitative determination of the material composition can supply useful information to restorers and help the object cataloguing. However, the analytical LIBS measurements on the archaeological materials were rarely reported, mainly due to difficulties to obtain the corresponding matrix-matched standards, required for the initial calibration. Alternatively, Calibration-Free (CF) approach could be used on some class of materials if all the major sample elements are detected and if the laser plasma preserves the material stochiometry. The latter condition is sometimes missing, as in the case of bronzes under nanosecond pulse laser ablation. We have developed a theoretical model for laser ablation of quaternary copper alloys, which allows for correction of the missing plasma stochiometry in CF approach. The model also predicts the optimal calibration for this type of material. In our recent work, we also obtained quantitative LIBS results on marbles by realizing the calibration standards starting from doped CaCO3 powders and by applying the corrections on the plasma parameters, different for the laboratory standards and marbles. Semi-quantitative LIBS results have been also obtained on multi-layered renaissance ceramics by subtraction of the contribution to plasma of each ceramic layer.

LIBS Analysis of Liquids and of Materials Inside Liquids

Laser induced plasma formation on or inside liquids is characterized by large energy losses due to liquid evaporation. Ablation of a liquid surface is followed by hydro-dynamical instabilities and splashing. Plasma generation inside bulk liquids is affected by the light absorption and scattering, and it is accompanied by intense pressure waves and successive vapor cavitation. Efficient LIBS analyses in presence of liquids require different considerations; the examples are reported and discussed in following.

Influence of the target material on secondary plasma formation underwater and its laser induced breakdown spectroscopy (LIBS) signal

The goal of this study was to investigate whether a secondary plasma can be formed on a non-metallic target under water and to give insight into the related processes. The material of choice here was alumina, since its physical, thermal and mechanical properties are substantially different from those of pure Al, only for which secondary plasma formation was recently demonstrated. To achieve this, plasma and bubble formation on alumina under water after single pulse laser excitation were studied using fast photography, shadowgraphy, Schlieren and LIBS techniques. The results show that the secondary plasma caused by backward heating of the target and successive slow target evaporation into the growing vapour bubble also occurs for alumina. The secondary plasma formed on alumina involves only a narrow interaction region on the target resulting in an almost spherical plume shape. In contrast, on thermally conductive and easily melting/evaporating aluminium, the secondary plasma is intense, with a large volume which is flattened on the target surface. Inside the expanded bubble above the alumina target, glowing particles were not observed. Due to less efficient secondary plasma formation on alumina compared to aluminium, its optical emission only slightly increases at a delay of 400 ns from the laser pulse but emission persists during three bubble cycles with a total duration of about 650 μs. The LIBS spectra related to the secondary plasma are almost free from any continuum component and show narrow emission lines from low excited states. Here we discuss the observed differences in the plasma’s spatial, temporal and spectral evolution on the two considered target materials. The obtained results indicate that under water a secondary plasma might be formed on very different materials and that its detection produces a good quality LIBS signal from single pulse excitation using a commercial nanosecond laser source.

Sample Preparation for Repeated Measurements on a Single Liquid Droplet Using Laser-Induced Breakdown Spectroscopy:

We studied changes in laser-induced breakdown spectroscopy (LIBS) signal intensity with the thickness of a liquid layer placed on a solid substrate, where an easily evaporating methanol sample was used. For a certain optimal liquid film thickness we obtained a manifold increase of the LIBS signal from methanol. Progressive liquid film thinning leads to a reduction and a successive disappearance of laser-induced splashes; the latter condition drastically reduces the sample consumption and allows measurements to be repeated many times on a single liquid droplet. In following, we developed two methods for actively controlled deformation, i.e., thinning of a liquid droplet (volume ∼10 µl) prior to its sampling by LIBS. Control of the droplet’s height was achieved on a Si–SiO2 wafer substrate by electro-wetting in the case of water solutions or by target rotation in the case of viscous liquids. The chosen substrate also has the advantages of low cost, easy manipulation, and very high purity, thus minimizing interference with analytes. Through the droplet deformation, in a single-pulse excitation at moderate laser energy (70 mJ), we clearly detected Fe and Mn in peanut oil, which represent trace elements in edible oils (∼ 1 part per billion), according to results published in the literature.

Standoff monitoring of aqueous aerosols using nanosecond laser-induced breakdown spectroscopy: droplet size and matrix effects

Nanosecond laser-induced breakdown spectroscopy has been examined for the analysis of suspended matter in a free stream of air. The real-time monitoring of this scenario poses major challenges for an accurate categorization due to its changing characteristics such as composition, size, and density of particles. The effects of particle size and matrix in the optical emission responses registered from such scenarios have been evaluated. Distant (10 m) plasmas of saline solutions, containing either NaCl or Na2SO4 at different concentrations, have been induced by nanosecond laser pulses at a wavelength of 1064 nm. The effects of the droplet size and its concentration on differences in the laser-induced breakdown probability, the intensity of the characteristic lines, and the plasma emission continuum have been discussed. The quantification of sodium in distant water droplets has been proved. However, an initial knowledge on the average droplet size is required. The average droplet size could be determined from the slope of H I and O I lines versus the continuum plasma emission, which is only weakly influenced by the salt content in the droplets.