Laser-induced breakdown spectroscopy; LIBS; Calibration-free LIBS; Limit of detection; Analytical sensitivity; Calibration; Spatial heterodyne spectroscopy;QUANTITATIVE-ANALYSIS; ELEMENTAL ANALYSIS; PLANT MATERIALS; MOISTURE-CONTENT; CARBON CONTENT; LIBS; COAL; IDENTIFICATION; SOIL; METHODOLOGY

The goal of this review article is to provide a description of recent and novel laser-induced breakdown spectroscopy (LIBS) applications and developments, especially those discussed during the NASLIBS Conference, held during SciX in Providence, RI, in September 2015. This topic was selected in view of the numerous recent overall review papers that have successfully given a broad view of the current understanding of laser-material interactions and plasma development and have also discussed the wide landscape of analytical applications of LIBS. This paper is divided into sections that focus on a few of the many applications under development in the LIBS community. We provide a summary of updates to calibration-free LIBS (CF-LIBS) and associated developments using plasma characteristics to improve quantification in LIBS output, both in a dedicated section and as applications are discussed. We have also described the most recent publications studying the sources, generation, and use of molecular features in LIBS, including those naturally present in the spectra of organic materials, and those induced with the addition of salts to enable the measurement of halogens, not typically present in LIBS signals. In terms of development of applications of LIBS, we focused on the use of LIBS for indirect measurements such as pH and degree of humification in soil and heating value in coal. We also reviewed the extant literature on LIBS analysis of agricultural materials, coal, minerals, and metals. Finally, we discuss the nascent developments of spatially heterodyne spectroscopy, a method that seeks to circumnavigate a serious drawback of most spectrometers - very small optical throughput - through the use of interferometers.

Laser-induced breakdown spectroscopy; remote LIBS; standoff LIBS; spatial heterodyne spectrometer; remote spectroscopy;IN-SITU ANALYSIS; RAMAN-SPECTROSCOPY; QUANTITATIVE-ANALYSIS; SOLID-SURFACES; SAMPLES; PLATFORM; PLASMA; SENSOR; PROBE

A spatial heterodyne spectrometer (SHS) is described for standoff laser-induced breakdown spectroscopy (LIBS) measurements. The spatial heterodyne LIBS spectrometer (SHLS) is a diffraction grating based interferometer with no moving parts that offers a very large field of view, high light throughput, and high spectral resolution in a small package. The field of view of the SHLS spectrometer is shown to be similar to 1 degrees in standoff LIBS measurements. In the SHLS system described here, the collection aperture was defined by the 10mm diffraction gratings in the SHS and standoff LIBS measurements were made up to 20m with no additional collection optics, corresponding to a collection solid angle of 0.2 mu sr, or f/2000, and also using a small telescope to increase the collection efficiency. The use of a microphone was demonstrated to rapidly optimize laser focus for 20m standoff LIBS measurements.

Laser-induced breakdown spectroscopy; LIBS; laser spectroscopy; paleoclimate;MYTILUS-EDULIS; PECTEN-MAXIMUS; DA COSTA; ICP-MS; SCLEROCHRONOLOGY; TEMPERATURE; SEASONALITY; CHALLENGES; CHEMISTRY; BIVALVIA

The chemical composition of mollusk shells offers information about environmental conditions present during the lifespan of the organism. Shells found in geological deposits and in many archeological sites can help to reconstruct past climatic conditions. For example, a correlation has been found between seawater temperature and the amount of some substituent elements (e.g., magnesium, strontium) in the biogenerated calcium carbonate matrix of the shell, although it is very species-specific. Here we propose the use laser-induced breakdown spectroscopy (LIBS) to estimate Mg/Ca ratios in modern specimens of the common limpet Patella vulgata. An automated setup was used to obtain a sequence of Mg/Ca ratios across a sampling path that could be compared with the seawater temperatures recorded during the organism's lifespan. Results using four shells collected in different months of the year showed a direct relationship between the Mg/Ca ratios and the seawater temperature, although the sequences also revealed small-scale (short-term) variability and an irregular growth rate. Nevertheless, it was possible to infer the season of capture and the minimum and maximum seawater temperatures from the LIBS sequences. This fact, along with the reduction in sampling and measurement time compared with other spectrometric techniques (such as inductively coupled plasma mass spectrometry [ICP-MS]), makes LIBS useful in paleoclimatic studies.

Laser-induced breakdown spectroscopy; LIBS; matrix effects; univariate calibration; minor elements; Cr; Ni; Co; Zn; Mn;GALE CRATER; MARS; SAMPLES

Obtaining quantitative chemical information using laser-induced breakdown spectroscopy is challenging due to the variability in the bulk composition of geological materials. Chemical matrix effects caused by this variability produce changes in the peak area that are not proportional to the changes in minor element concentration. Therefore the use of univariate calibrations to predict trace element concentrations in geological samples is plagued by a high degree of uncertainty. This work evaluated the accuracy of univariate minor element predictions as a function of the composition of the major element matrices of the samples and examined the factors that limit the prediction accuracy of univariate calibrations. Five different sample matrices were doped with 10-85 000 ppm Cr, Mn, Ni, Zn, and Co and then independently measured in 175 mixtures by X-ray fluorescence, inductively coupled plasma atomic emission spectrometry, and laser-induced breakdown spectroscopy, the latter at three different laser energies (1.9, 2.8, and 3.7 mJ). Univariate prediction models for minor element concentrations were created using varying combinations of dopants, matrices, normalization/no normalization, and energy density; the model accuracies were evaluated using root mean square prediction errors and leave-one-out cross-validation. The results showed the superiority of using normalization for predictions of minor elements when the predicted sample and those in the training set had matrices with similar SiO2 contents. Normalization also mitigates differences in spectra arising from laser/sample coupling effects and the use of different energy densities. Prediction of minor elements in matrices that are dissimilar to those in the training set can increase the uncertainty of prediction by an order of magnitude. Overall, the quality of a univariate calibration is primarily determined by the availability of a persistent, measurable peak with a favorable transition probability that has little to no interference from neighboring peaks in the spectra of both the unknown and those used to train it.

Laser-induced breakdown spectroscopy; LIBS; elemental identification; wavelength similarity coefficient;SEARCH ALGORITHMS; SPECTROSCOPY; PLASMA; LIBRARY

This work proposes a method to perform elemental identification on plasmas produced using the laser-induced breakdown spectroscopy (LIBS) technique. The method is based on the preservation of the relative relevance of the spectral line emission intensities, which is lost during the parametric correlation procedure, by the introduction of a similitude coefficient called wavelength similarity coefficient. Furthermore, it was shown that for identification purposes, a simplified plasma model is sufficient to predict adequately the relative emission intensities in LIBS plasmas. As a result, it is possible to automatically identify the species with high emission signals, while trace detection is also possible by relaxing search conditions, although manual refinement is still required.

Laser-induced breakdown spectroscopy; LIBS; lens-to-sample distance; sample positioning; repeatability;

A simple device based on two commercial laser pointers is described to assist in the analysis of samples that present uneven surfaces and/or irregular shapes using laser-induced breakdown spectroscopy (LIBS). The device allows for easy positioning of the sample surface at a reproducible distance from the focusing lens that conveys the laser pulse to generate the micro-plasma in a LIBS system, with reproducibility better than +/- 0.2 mm. In this way, fluctuations in the fluence (J cm(-2)) are minimized and the LIBS analytical signals can be obtained with a better precision even when samples with irregular surfaces are probed.

Laser-induced breakdown spectroscopy; LIBS; self-absorption; curve-of-growth; COG;INDUCED PLASMA; GROWTH; CURVES

Laser-induced breakdown spectroscopy (LIBS) is a widely used laser spectroscopic technique in various fields, such as material science, forensic science, biological science, and the chemical and pharmaceutical industries. In most LIBS work, the analysis is performed using radiative transitions from atomic emissions. In this study, the plasma temperature and the product Nl (the number density N and the absorption path length l) were determined to evaluate the optical depths and the self-absorption of Sr and Al lines. A binary mixture of strontium nitrate and aluminum oxide was used as a sample, consisting of variety of different concentrations in powder form. Laser-induced breakdown spectroscopy spectra were collected by varying various parameters, such as laserenergy, gate delay time, and gate width time to optimize the LIBS signals. Atomic emission from Sr and Al lines, as observed in the LIBS spectra of different sample compositions, was used to characterize the laser induced plasma and evaluate the optical depths and self-absorption of LIBS.

Edible salt; sulfur; laser ablation sampling; laser-induced breakdown spectroscopy; LIBS; laser ablation inductively coupled optical emission spectrometry; LA-ICP-OES; laser ablation inductively coupled plasma mass spectrometry; LA-ICP-MS;INDUCED BREAKDOWN SPECTROSCOPY; REINFORCED-CONCRETE STRUCTURES; PLASMA-MASS-SPECTROMETRY; SEA SALTS; ELEMENTS; CLASSIFICATION; INTENSITY; CHLORINE; SODIUM; ORIGIN

We evaluated the performance of laser ablation analysis techniques such as laser-induced breakdown spectroscopy (LIBS), laser ablation inductively coupled optical emission spectrometry (LA-ICP-OES), and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), in comparison with that of ICP-OES using aqueous solutions for the quantification of sulfur (S) in edible salts from different geographical origins. We found that the laser ablation based sampling techniques were not influenced by loss of S, which was observed in ICP-OES with aqueous solutions for a certain salt upon their dissolution in aqueous solutions, originating from the formation of volatile species and precipitates upon their dilution in water. Although detection of S using direct lasersampling with LA-ICP-MS has well-known isobaric and polyatomic interferences, LIBS and LA-ICP-OES showed good accuracy in the detection of S for all salts. LIBS also provided the ability to identify the dominant chemical form in which S is present in salts. Correlation between S and oxygen, oserved in LIBS spectra, provided chemical information about the presence of S2- or SO42-, which are associated with the origin and quality of edible salts.

Laser-induced breakdown spectroscopy; femtosecond LIBS; fs-LIBS; amalgam; dental restoration; mercury;INDUCED BREAKDOWN SPECTROSCOPY; RESTORATIVE DECISION-MAKING; RESIN-BASED COMPOSITE; PERMANENT TEETH; DENTAL AMALGAM; GLASS-IONOMER; LONGEVITY; REPLACEMENT; TOXICOLOGY; MIGRATION

In this work the diffusion of mercury and other elements from amalgam tooth restorations through the surrounding dental tissue (dentin) was evaluated using femtosecond laser-induced breakdown spectroscopy (fs-LIBS). To achieve this, seven deciduous and eight permanent extracted human molar teeth with occlusal amalgam restorations were half-sectioned and analyzed using pulses from a femtosecond laser. The measurements were performed from the amalgam restoration along the amalgam/dentin interface to the apical direction. It was possible to observe the presence of metallic elements (silver, mercury, copper and tin) emission lines, as well as dental constituent ones, providing fingerprints of each material and comparable data for checking the consistence of the results. It was also shown that the elements penetration depth values in each tooth are usually similar and consistent, for both deciduous and permanent teeth, indicating that all the metals diffuse into the dentin by the same mechanism. We propose that this diffusion mechanism is mainly through liquid dragging inside the dentin tubules. The mercury diffused further in permanent teeth than in deciduous teeth, probably due to the longer diffusion times due to the age of the restorations. It was possible to conclude that the proposed femtosecond-LIBS system can detect the presence of metals in the dental tissue, among the tooth constituent elements, and map the distribution of endogenous and exogenous chemical elements, with a spatial resolution that can be brought under 100 mu m.

Laser-induced breakdown spectroscopy; LIBS; liquid; plasma; laser ablation;AQUEOUS-SOLUTIONS; VEGETABLE-OILS; WASTE-WATER; LIBS; METALS; ELEMENTS; SODIUM; PLASMA; PULSE; ACIDS

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 similar to 10 ml) 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 (similar to 1 part per billion), according to results published in the literature.

Raman; laser-induced breakdown spectroscopy; LIBS; matrix effect; geological samples;QUANTITATIVE-ANALYSIS; SPECTROMETER; MIXTURES

Quantitative Raman analysis was carried out with geologically mixed samples that have various matrices. In order to compensate the matrix effect in Raman shift, laser-induced breakdown spectroscopy (LIBS) analysis was performed. Raman spectroscopy revealed the geological materials contained in the mixed samples. However, the analysis of a mixture containing different matrices was inaccurate due to the weak signal of the Raman shift, interference, and the strong matrix effect. On the other hand, the LIBS quantitative analysis of atomic carbon and calcium in mixed samples showed high accuracy. In the case of the calcite and gypsum mixture, the coefficient of determination of atomic carbon using LIBS was 0.99, while the signal using Raman was less than 0.9. Therefore, the geological composition of the mixed samples is first obtained using Raman and the LIBS-based quantitative analysis is then applied to the Raman outcome in order to construct highly accurate univariate calibration curves. The study also focuses on a method to overcome matrix effects through the two complementary spectroscopic techniques of Raman spectroscopy and LIBS.

Gunshot residue; laser-induced breakdown spectroscopy; LIBS; evidence preservation; scanning electron microscopy energy dispersive X-ray spectroscopy; SEM-EDX;HANDS; AMMUNITION; SHOOTER

This study investigated the use of laser-induced breakdown spectroscopy (LIBS) and scanning electron microscopy energy dispersive X-ray spectroscopy(SEM-EDX) as means of characterizing gunshot residue (GSR) originating from commercially available lead-free rounds. Data from two experiments are presented in this work. One experiment focused on identifying prominent analytical markers present in lead-free GSR by LIBS while the other applied SEM-EDX to determine the degree of evidence preservation after LIBS analysis. Samples of GSR were collected via tape-lift method from the hands of volunteer shooters and instrumental analyses were conducted in triplicate. As a result, the lead-free ammunition analyzed in this work generated GSRs comprising primarily Ba, Al, Si, and/or K. Trace amounts of Ti, Fe, and S were also apparent in some compositions. Through SEM-EDX analysis, a spheroidal geometry consistent with traditional lead-containing GSR was observed. Additionally, it was determined that evidence is preserved after LIBS analysis which supports the implementation of LIBS as a rapid preliminary screening method followed by confirmatory testing via SEM-EDX on the preserved evidence.

Laser-induced breakdown spectroscopy; LIBS; long-wave infrared spectra; explosives;ARRAY DETECTION SYSTEM; ENERGETIC MATERIALS; SPECTRA; PHASE; ACID; HMX

Thin solid films made of high nitro (NO2)/nitrate (NO3) content explosives were deposited on sand-blasted aluminum substrates and then studied using a mercury-cadmium-telluride (MCT) linear array detection system that is capable of rapidly capturing a broad spectrum of atomic and molecular laser-inducedbreakdown spectroscopy (LIBS) emissions in the long-wave infrared region (LWIR; similar to 5.6-10 mm). Despite the similarities of their chemical compositions and structures, thin films of three commonly used explosives (RDX, HMX, and PETN) studied in this work can be rapidly identified in the ambient air by their molecular LIBS emission signatures in the LWIR region. A preliminary assessment of the detection limit for a thin film of RDX on aluminum appears to be much lower than 60 mg/cm(2). This LWIR LIBS setup is capable of rapidly probing and charactering samples without the need for elaborate sample preparation and also offers the possibility of a simultaneous ultraviolet visible and LWIR LIBS measurement.

Laser-induced breakdown spectroscopy; nuclear safeguards; pyroprocessing; molten salts;LIQUIDS

In the pyrochemical separation of used nuclear fuel (UNF), fission product, rare earth, and actinide chlorides accumulate in the molten salt electrolyte over time. Measuring this salt composition in near real-time is advantageous for operational efficiency, material accountability, and nuclear safeguards. Laser-induced breakdown spectroscopy (LIBS) has been proposed and demonstrated as a potential analytical approach for molten LiCl-KCl salts. However, all the studies conducted to date have used a static surface approach which can lead to issues with splashing, low repeatability, and poor sample homogeneity. In this initial study, a novel molten salt aerosol approach has been developed and explored to measure the composition of the salt via LIBS. The functionality of the system has been demonstrated as well as a basic optimization of the laser energy and nebulizer gas pressure used. Initial results have shown that this molten salt aerosol-LIBS system has a great potential as an analytical technique for measuring the molten salt electrolyte used in this UNF reprocessing technology.

Laser-induced breakdown spectroscopy; LIBS; safeguards; pyroprocessing; molten salt; cerium; gadolinium;MELT CRYSTALLIZATION; MOLTEN-SALT; STRONTIUM; CESIUM

Pyroprocessing of used nuclear fuel (UNF) has many advantages-including that it is proliferation resistant. However, as part of the process, special nuclear materials accumulate in the electrolyte salt and present material accountability and safeguards concerns. The main motivation of this work was to explore a laser-induced breakdown spectroscopy (LIBS) approach as an online monitoring technique to enhance the material accountability of special nuclear materials in pyroprocessing. In this work, a vacuum extraction method was used to draw the molten salt (CeCl3-GdCl3-LiCl-KCl) up into 4 mm diameter Pyrex tubes where it froze. The salt was then removed and the solid salt was measured using LIBS and inductively coupled plasma mass spectroscopy (ICP-MS). A total of 36 samples were made that varied the CeCl3 and GdCl3 (surrogates for uranium and plutonium, respectively) concentrations from 0.5 wt% to 5 wt%. From these samples, univariate calibration curves for Ce and Gd were generated using peak area and peak intensity methods. For Ce, the Ce 551.1 nm line using the peak area provided the best calibration curve with a limit of detection (LOD) of 0.099 wt% and a root mean squared error of cross-validation (RMSECV) of 0.197 wt%. For Gd, the best curve was generated using the peak intensities of the Gd 564.2 nm line resulting in a LOD of 0.027 wt% and a RMSECV of 0.295 wt%. The RMSECV for the univariate cases were determined using leave-one-out cross-validation. In addition to the univariate calibration curves, partial least squares (PLS) regression was done to develop a calibration model. The PLS models yielded similar results with RMSECV (determined using Venetian blind cross-validation with 17% left out per split) values of 0.30 wt% and 0.29 wt% for Ce and Gd, respectively. This work has shown that solid pyroprocessing salt can be qualitatively and quantitatively monitored using LIBS. This work has the potential of significantly enhancing the material monitoring and safeguards of special nuclear materials in pyroprocessing.

Long pulse; dual-pulse laser-induced breakdown spectroscopy; DP-LIBS; enhancement; plasma temperature stabilization; underwater measurement;CO2-LASER PULSE; AMBIENT GAS; ABLATION; ENHANCEMENT; PRESSURES; FEASIBILITY; MAGNESIUM; DISCHARGE; SPECTRUM; LIQUIDS

Collinear long and short dual-pulse laser-induced breakdown spectroscopy (DP-LIBS) was employed to clarify the emission characteristics from laser-inducedplasma. The plasma was sustained and became stable by the long pulse-width laser with the pulse width of 60s under free running (FR) conditions as an external energy source. Comparing the measurement results of stainless steel in air using single-pulse LIBS (SP-LIBS) and DP-LIBS, the emission intensity was markedly enhanced using DP-LIBS. The temperature of plasma induced by DP-LIBS was maintained at a higher temperature under different gate delay time and short pulse-width laser power conditions compared with those measured using short SP-LIBS. Moreover, the variation rates of plasma temperatures measured using DP-LIBS were also lower. The superior detection ability was verified by the measurement of aluminum sample in water. The spectra were clearly detected using DP-LIBS, whereas it cannot be identified using SP-LIBS of short and long pulse widths. The effects of gate delay time and short pulse-width laser power were also discussed. These results demonstrate the feasibility and enhanced detection ability of the proposed collinear long and short DP-LIBS method.

Laser-induced breakdown spectroscopy; LIBS; multivariate analysis; soft independent modeling of class analogy; SIMCA; partial least squares discriminant analysis; PLS-DA; edible salt;INDUCED BREAKDOWN SPECTROSCOPY; SEA SALTS; LIBS; IDENTIFICATION; COMPACT; ORIGIN

We report soft independent modeling of class analogy (SIMCA) analysis of laser-induced plasma emission spectra of edible salts from 12 different geographical origins for their classification model. The spectra were recorded by using a simple laser-induced breakdown spectroscopy (LIBS) device. Each class was modeled by principal component analysis (PCA) of the LIBS spectra. For the classification of a separate test data set, the SIMCA model showed 97% accuracy in classification. An additional insight could be obtained by comparing the SIMCA classification result with that of partial least squares discriminant analysis (PLS-DA). Different from SIMCA, the PLS-DA classification accuracy seems to be sensitive to addition of new sample classes to the whole data set. This indicates that the individual modeling approach (SIMCA) can be an alternative to global modeling (PLS-DA), particularly for the classification problems with a relatively large number of sample classes.

Laser-induced breakdown spectroscopy; LIBS; wines; matrix effect; trace elements;ATOMIC-ABSORPTION-SPECTROMETRY; X-RAY-FLUORESCENCE; LIQUID-LIQUID MICROEXTRACTION; QUANTITATIVE-DETERMINATION; SAMPLE INTRODUCTION; AQUEOUS-SOLUTIONS; TRACE-ELEMENTS; SINGLE-PULSE; ICP-OES; CLASSIFICATION

We developed a method for sensitive elemental analysis of wines using laser-induced breakdown spectroscopy (LIBS). In order to overcome the inefficiency of direct ablation of bulk wine (an organic liquid), a thin layer of wine residue was prepared on a metallic target according to an appropriated heating procedure applied to an amount of liquid wine dropped on the target surface. The obtained ensemble was thus ablated. Such a sample preparation procedure used a very small volume of 2mL of wine and took only 30min without reagent or solvent. The results show the detection of tens of metal and non-metal elements including majors (Na, Mg, K, Ca), minors, and traces (Li, B, Si, P, Ti, Mn, Fe, Cu, Zn, Rb, Sr, Ba, and Pb) in wines purchased from local supermarkets and from different production places in France. Commercially available wines were then spiked with certified standard solutions of Ti and Fe. Three series of laboratory reference samples were thus prepared using three different wines (a red wine and a white wine from a same production region and a red wine from another production region) with concentrations of Ti and Fe in the range of 1-40mg/L. Calibration graphs established with the spiked samples allowed extracting the figures-of-merit parameters of the method for wine analysis such as the coefficient of determination (R-2) and the limits of detection and quantification (LOD and LOQ). The calibration curves built with the three wines were then compared. We studied the residual matrix effect between these wines in the determination of the concentrations of Ti and Fe.

Laser-induced breakdown spectroscopy; LIBS; in situ K-Ar dating; planetary missions; Mars; geochronology; instrument development; potassium measurements;CHEMCAM INSTRUMENT SUITE; MASS-SPECTROMETRY; MARS; ROCKS; CHRONOLOGY; EVOLUTION; SYSTEM; UNIT

In situ radiogenic isotope measurements to obtain the absolute age of geologic events on planets are of great scientific value. In particular, K-Ar isochrons are useful because of their relatively high technical readiness and high accuracy. Because this isochron method involves spot-by-spot K measurements using laser-induced breakdown spectroscopy (LIBS) and simultaneous Ar measurements with mass spectrometry, LIBS measurements are conducted under a high vacuum condition in which emission intensity decreases significantly. Furthermore, using a laser power used in previous planetary missions is preferable to examine the technical feasibility of this approach. However, there have been few LIBS measurements for K under such conditions. In this study, we measured K contents in rock samples using 30mJ and 15mJ energy lasers under a vacuum condition (10(-3)Pa) to assess the feasibility of in situ K-Ar dating with lasers comparable to those used in NASA's Curiosity and Mars 2020 missions. We obtained various calibration curves for K using internal normalization with the oxygen line at 777nm and continuum emission from the laser-induced plasma. Experimental results indicate that when K2O<1.1wt%, a calibration curve using the intensity of the K emission line at 769nm normalized with that of the oxygen line yields the best results for the 30mJ laser energy, with a detection limit of 88ppm and 20% of error at 2400ppm of K2O. Futhermore, the calibration curve based on the K 769nm line intensity normalized with continuum emission yielded the best result for the 15mJ laser, giving a detection limit of 140ppm and 20% error at 3400ppm K2O. Error assessments using obtained calibration models indicate that a 4 Ga rock with 3000ppm K2O would be measured with 8% (30mJ) and 10% (15mJ) of precision in age when combined with mass spectrometry of Ar-40 with 10% of uncertainty. These results strongly suggest that high precision in situ isochron K-Ar dating is feasible with a laser used in previous and upcoming Mars rover missions.

Calibration-free laser-induced breakdown spectroscopy; CF-LIBS; self-absorption; Saha-Boltzmann; Stark broadening; standard reference line;QUANTITATIVE ELEMENTAL ANALYSIS; INDUCED PLASMA SPECTROSCOPY; SELF-ABSORPTION; SPECTRAL-LINES; TEMPERATURE; ACCURACY; ALUMINUM

In this work, calibration-free laser-induced breakdown spectroscopy (CF-LIBS) is used to analyze a certified stainless steel sample. Due to self-absorption of the spectral lines from the major element Fe and the sparse lines of trace elements, it is usually not easy to construct the Boltzmann plots of all species. A standard reference line method is proposed here to solve this difficulty under the assumption of local thermodynamic equilibrium so that the same temperature value for all elements present into the plasma can be considered. Based on the concentration and rich spectral lines of Fe, the Stark broadening of Fe(I) 381.584nm and Saha-Boltzmann plots of this element are used to calculate the electron density and the plasma temperature, respectively. In order to determine the plasma temperature accurately, which is seriously affected by self-absorption, a pre-selection procedure for eliminating those spectral lines with strong self-absorption is employed. Then, one spectral line of each element is selected to calculate its corresponding concentration. The results from the standard reference lines with and without self-absorption of Fe are compared. This method allows us to measure trace element content and effectively avoid the adverse effects due to self-absorption.

Laser-induced breakdown spectroscopy; LIBS; Plasma confinement; signal-to-noise ratio; signal precision;INDUCED BREAKDOWN SPECTROSCOPY; OPTICAL-EMISSION; GALVANIZED STEEL; ENHANCEMENT; IMPROVEMENT; EXCITATION; LIBS; SENSITIVITY; ABLATION; PULSES

The present work focuses on the influence of the angle of observation on the emission signal from copper plasmas. Plasma plumes have been generated inside a home-made chamber consisting of two parallel glass windows spaced by 2.5mm. This chamber allows observing plasma plumes from different collection angles throughout their perimeter, spanning from 20 degrees to 80 degrees with respect to the surface of the Cu target. In order to minimize the observed volume of the plasma, measurements were made from the closest distance possible through a metallic hollow tube. Single-pulse and collinear double-pulse excitation schemes with a Nd:YAG laser (1064nm, 5ns) have been investigated. The results have shown that the selection of the best angle to collect light from the plasma is related to the excitation mode. On the other hand, the shot-to-shot signal variability has been found to depend on the shape of plasma plumes. In single-pulse excitation, a good correlation between the observed laser-induced breakdown spectroscopy (LIBS) emission (from spatially confined plumes) and their integrated signal of plasma image has been ascertained. However, this fact was less evident in double-pulse LIBS, which could be due to a different mechanism involved in the ablation process.

Baseline removal; Raman spectroscopy; laser-induced breakdown spectroscopy; LIBS; very near; infrared spectroscopy; VNIR;X-RAY-SPECTRA; LEAST-SQUARES; RAMAN-SPECTRA; NMR-SPECTRA; RECOGNITION; SUBTRACTION; REGRESSION; ALGORITHM

The task of proper baseline or continuum removal is common to nearly all types of spectroscopy. Its goal is to remove any portion of a signal that is irrelevant to features of interest while preserving any predictive information. Despite the importance of baseline removal, median or guessed default parameters are commonly employed, often using commercially available software supplied with instruments. Several published baseline removal algorithms have been shown to be useful for particular spectroscopic applications but their generalizability is ambiguous. The new Custom Baseline Removal (Custom BLR) method presented here generalizes the problem of baseline removal by combining operations from previously proposed methods to synthesize new correction algorithms. It creates novel methods for each technique, application, and training set, discovering new algorithms that maximize the predictive accuracy of the resulting spectroscopic models. In most cases, these learned methods either match or improve on the performance of the best alternative. Examples of these advantages are shown for three different scenarios: quantification of components in near-infrared spectra of corn and laser-induced breakdown spectroscopydata of rocks, and classification/matching of minerals using Raman spectroscopy. Software to implement this optimization is available from the authors. By removing subjectivity from this commonly encountered task, Custom BLR is a significant step toward completely automatic and general baseline removal in spectroscopic and other applications.

Nutritional evaluation; laser-induced breakdown spectroscopy; LIBS; Huanglongbing; HLB; phytosanitary control; diagnosis; data analysis; citrus diseases;GREENING DISEASE; FLUORESCENCE; LIBS; LEAVES; TOOLS

Huanglongbing (HLB) is the most recent and destructive bacterial disease of citrus and has no cure yet. A promising alternative to conventional methods is to use laser-induced breakdown spectroscopy (LIBS), a multi-elemental analytical technique, to identify the nutritional changes provoked by the disease to the citrus leaves and associate the mineral composition profile with its health status. The leaves were collected from adult citrus trees and identified by visual inspection as healthy, HLB-symptomatic, and HLB-asymptomatic. Laser-induced breakdown spectroscopy measurements were done in fresh leaves without sample preparation. Nutritional variations were evaluated using statistical tools, such as Student's t-test and analysis of variance applied to LIBS spectra, and the largest were found for Ca, Mg, and K. Considering the nutritional profile changes, a classifier induced by classification via regression combined with partial least squares regression was built resulting in an accuracy of 73% for distinguishing the three categories of leaves.