Laser-induced breakdown spectroscopy: Time-resolved spectrochemical applications

We have added time resolution to laser-induced breakdown spectroscopy in two forms, by gating an optical multichannel analyzer (OMA) and by time-resolving the output of a photomultiplier with a boxcar amplifier. Spectra were obtained for temporal segments of 25 to 100 ns, from 25 ns to 50 µs after initiation of the breakdown. OMA spectra of oxygen illustrate the power of this technique for survey purposes. The photomultiplier-boxcar arrangement was used to detect phosphorus atoms from diisopropylmethyl phosphonate in air, and also to detect chlorine in air, both in real time. In the former experiments we detected 690 ppm (w/w) of phosphorus and project a limit of detection with our current apparatus of 15 ppm (w/w). For chlorine, we observed signal from 120 ppm (w/w) and project a limit of detection of 60 ppm (w/w).     

Determination of lead in water using laser ablation–laser induced fluorescence

The detection sensitivity of laser-induced breakdown spectroscopy (LIBS) is improved by coupling it with a laser-induced fluorescence method. A waterjet sample containing 500 ppm of Pb as an analyte was ablated by a 266 nm, frequency-quadrupled Q-switchedNd:YAG laser at an energy of ~ 260 μJ. After a short delay the resulting plume was re-excited with a 283.306 nm, nanosecond pulse dye laser at energies ranging from 45 to 100 nJ. The limit of detection (LOD) of lead in water was determined both by the single-pulse LIBS technique and Laser Ablation coupled with Laser-Induced Fluorecence (LA–LIF) method. It was found to be 75 ppm in the case of single-pulse LIBS and 4.3 ppm for LA–LIF. When the resonant pulse was detuned from the transition wavelength the LA–LIF signal disappeared demonstrating the resonant selectivity of this technique.     

Laser-induced breakdown spectroscopy for detection of explosives residues: a review of recent advances, challenges, and future prospects

In this review we discuss the application of laser-induced breakdown spectroscopy (LIBS) to the problem of detection of residues of explosives. Research in this area presented in open literature is reviewed. Both laboratory and field-tested standoff LIBS instruments have been used to detect explosive materials. Recent advances in instrumentation and data analysis techniques are discussed, including the use of double-pulse LIBS to reduce air entrainment in the analytical plasma and the application of advanced chemometric techniques such as partial least-squares discriminant analysis to discriminate between residues of explosives and non-explosives on various surfaces. A number of challenges associated with detection of explosives residues using LIBS have been identified, along with their possible solutions. Several groups have investigated methods for improving the sensitivity and selectivity of LIBS for detection of explosives, including the use of femtosecond-pulse lasers, supplemental enhancement of the laser-induced plasma emission, and complementary orthogonal techniques. Despite the associated challenges, researchers have demonstrated the tremendous potential of LIBS for real-time detection of explosives residues at standoff distances. Figure This review discusses the application of laser-induced breakdown spectroscopy (LIBS) to the problem of explosive residue detection. LIBS offers the capability for real-time, standoff detection of trace amounts of residue explosives on various surfaces     

Detection of trace concentrations of helium and argon in gas mixtures by laser-induced breakdown spectroscopy

We report what we believe to be the first demonstration of the detection of trace quantities of helium and argon in binary and ternary gas mixtures with nitrogen by laser-induced breakdown spectroscopy (LIBS). Although significant quenching of helium transitions due to collisional deactivation of excited species was observed, it was found that losses in analytical sensitivity could be minimized by increasing the laser irradiance and decreasing the pressure at which the analyses were performed. In consequence, limits of detection of parts-per-million and tens of parts-per-million and linear dynamic ranges of several orders of magnitude in analyte concentration were obtained. The results of this study suggest that LIBS may have potential applications in the detection of other noble gases at trace concentrations.     

Application of laser-induced breakdown spectrometry in urban health

The use of laser-induced breakdown spectrometry (LIBS) for elemental determination and detection in urban health is reviewed. It highlights the unique use of LIBS in fiber-based optics, in process control, and for field instrumentation. Selected applications confirm that LIBS could be the technique of choice for many applications in urban health.     

Laser-induced fluorescence detection of lead atoms in a laser-induced plasma: An experimental analytical optimization study

The combination of the laser-induced breakdown spectroscopy (LIBS) and laser-induced fluorescence (LIF) techniques was investigated to improve the limit of detection (LoD) of trace elements in solid matrices. The influence of the main experimental parameters on the LIF signal, namely the ablation fluence, the excitation energy, and the inter-pulse delay, was studied experimentally and a discussion of the results was presented. For illustrative purpose we considered detection of lead in brass samples. The plasma was produced by a Q-switched Nd:YAG laser and then re-excited by a nanosecond Optical Parametric Oscillator (OPO) laser. The experiments were performed in air at atmospheric pressure. We found out that the optimal conditions were obtained for our experimental set-up using relatively weak ablation fluence of 2–3 J/cm² and an inter-pulse delay of about 5–10 μs. Also, a few tens of microjoules was typically required to maximize the LIF signal. Using the LIBS–LIFS technique, a single-shot LoD for lead of about 1.5 part per million (ppm) was obtained while a value of 0.2 ppm was obtained after accumulating over 100 shots. These values represent an improvement of about two orders of magnitude with respect to LIBS.     

Analysis of laser-induced breakdown images measuring the sizes of mixed aquatic nanoparticles

Sizes of aquatic colloidal nanoparticles are determined by utilizing the laser-induced breakdown detection technique. Specifically, the number of breakdown events is measured as a function of area in laser-induced plasma images, generated from a mixture of two different size nanoparticles in aqueous solution, by minimizing the energy of the incident laser irradiation to generate the plasma. We find that the accuracy of measuring the sizes of nanoparticles in mixtures is greatly improved when selecting the plasma images produced only within one-half of the Rayleigh range of the focused Gaussian beam where the irradiation is most uniformly distributed.     

Quantitative analysis by resonant laser ablation with optical emission detection: Resonant laser-induced breakdown spectroscopy

Resonant laser ablation (RLA) is a solid sampling technique that makes use of radiation trapping, and desorption induced by electronic transitions (DIET), to produce enhanced numbers of analyte atoms in the laser-induced plasma (LIP). This is achieved by tuning the laser ablation wavelength to a gas-phase resonant transition of the analyte. In this paper, RLA was coupled with detection of optical emission in the LIP to perform resonant laser-induced breakdown spectroscopic (RLIBS) experiments with a miniature, portable spectrometer. The experiments were designed to continue an examination of the proposed mechanism of RLA, and to perform an initial assessment of the applicability of RLIBS for quantitative analysis. The study indicated that for a multi-component sample, such as steel, the signal of the wavelength-targeted atom was enhanced the most compared to other constituents, and this supported the hypothesis that the DIET phenomenon is involved. Also, RLIBS experiments indicated that ablation yields of other components were enhanced by resonant ablation of the major component, which supported the contribution of radiation trapping to the RLA phenomenon. A linear, positive slope of the RLA induced atom yield as a function of concentration suggested that the RLA mechanism allows for quantitative analysis of solid samples. Calibration graphs were created for tungsten in spectrographic steels using RLIBS. A limit of detection of 4% was calculated for tungsten in steel.     

Characterization of coal fly ash components by laser-induced breakdown spectroscopy

The high sensitivity of laser-induced breakdown spectroscopy (LIBS) for the detection of most of the fly ash components enables the analysis of these residues produced during the combustion of coal. Fly ash consists of oxides (SiO₂, Al₂O₃, Fe₂O₃, CaO…) and unburnt carbon which is the major determinant of combustion efficiency in coal fired boilers. For example, an excessive amount of residual carbon dispersed in the fly ash means a significant loss of energy (Styszko et al., 2004 [1]). Standard methods employed for the analysis of fly ash make not possible a control of boiler in real time. LIBS technique can significantly reduce the time of analysis, in some cases even an online detection can be performed. For this reason, some studies have been addressed in order to demonstrate the capability of the laser-induced breakdown spectroscopy technique for the detection of carbon content in high pressure conditions typical of thermal power plants (Noda et al., 2002 [2]) and for the monitoring of unburnt carbon for the boiler control in real time (Kurihara et al., 2003[3]).In particular, the content of unburnt carbon is a valuable indicator for the control of fly ash quality and for the boiler combustion. Depending on this unburnt carbon content, fly ash can be disposed as an industrial waste or as a raw material for the production of concrete in the construction sector. In this study, analyses were performed on specimens of various forms of preparation. Pressed pellets were prepared with two different binders. Presented results concern the nature and amount of the binder used to pelletize the powder, and the laser-induced breakdown spectroscopy parameters and procedure required to draw calibration curves of elements from the fly ash. Analysis “on tape” was performed in order to establish the experimental conditions for the future “online analysis”.     

Determination of size, concentration and elemental composition of colloids with laser-induced breakdown detection/spectroscopy (LIBD/S)

The application of laser-induced breakdown detection (LIBD) as a new and powerful particle-analyzing technique for the determination of solubility data by monitoring initial colloid generation, when the metal ion concentration just exceeds the solubility at a given pH value, is investigated. Laser-induced breakdown spectroscopy (LIBS) is used for selective analysis of an aqueous suspension of lanthanide oxide particles in the presence of the respective lanthanide aquo ion. The detection limit for aquo ion and oxide particle is determined. On the basis of the different detection limits, the LIBS technique is used to study the formation of hydroxide colloids in aqueous solution by varying the pH value until the solubility limit is exceeded. LIBS enables both qualitative and quantitative monitoring of particle formation without artifacts arising from other contaminants. LIBD and LIBS are described and compared. The advantages and disadvantages of the methods for the determination of solubility data are discussed.     

Analysis of lead and sulfur in environmental samples by double pulse laser induced breakdown spectroscopy

In the present work, a model of double pulse laser-induced breakdown spectroscopy (LIBS) spectrometer has been developed and results from two different applications of double pulse LIBS for solving the problems of environmental interest are presented. In one case, laser induced breakdown spectroscopy has been applied to the determination of heavy and toxic metals (lead) in soil samples. In the second case, laser induced breakdown spectroscopy was used in preliminary experiments for the detection of sulfur content in coal, and on the basis of spectral features, ways to improve the sensitivity of laser induced breakdown spectroscopy detection of sulfur are proposed. The detection limit for lead in soil was estimated to be approximately 20 ppm that is lower than the regulatory standards for the presence of lead in soil.     

Laser-induced breakdown spectroscopy (LIBS) for carbon single shot analysis of micrometer-sized particles

The purpose of this work is to study the ability of the laser-induced breakdown spectroscopy (LIBS) technique to perform in situ (without sample preparation) detection of graphite particles circulating in a gas loop used to simulate the cooling gas circuit of a helium-cooled nuclear reactor. Results obtained with a laboratory scale set up are presented. The experiments were performed in nitrogen with micrometer-sized particles containing carbon (glucose particles and sodium hydrogenocarbonate particles). Statistical shot to shot analysis was used to determine the concentration of the analyte. The variation of LIBS signal as a function of glucose particle diameter showed an underestimation of the signal of particles of diameters larger than 5 μm. This phenomenon is likely to be correlated to an incomplete vaporization in the laser-induced plasma of particles of sizes above 5 μm. Analytical measurements were performed with glucose particles and sodium hydrogenocarbonate particles, and the concentration-based limit of detection of carbon was evaluated to be about 60 μg m⁻³.     

Time-resolved characterization of laser-induced plasma from fresh potatoes

Optical emission of laser-induced plasma on the surface of fresh vegetables provides sensitive analysis of trace elements for in situ or online detection of these materials. This emergent technique promises applications with expected outcomes in food security or nutrition quality, as well as environment pollution detection. Characterization of the plasma induced on such soft and humid materials represents the first step towards quantitative measurement using this technique. In this paper, we present the experimental setup and protocol that optimize the plasma generation on fresh vegetables, potatoes for instance. The temporal evolution of the plasma properties are investigated using time-resolved laser-induced breakdown spectroscopy (LIBS). In particular, the electron density and the temperatures of the plasma are reported as functions of its decay time. The temperatures are evaluated from the well known Boltzmann and Saha-Boltzmann plot methods. These temperatures are further compared to that of the typical molecular species, CN, for laser-induced plasma from plant materials. This comparison validates the local thermodynamic equilibrium (LTE) in the specific case of fresh vegetables ablated in the typical LIBS conditions. A study of the temporal evolution of the signal to noise ratio also provides practical indications for an optimized detection of trace elements. We demonstrate finally that, under certain conditions, the calibration-free LIBS procedure can be applied to determine the concentrations of trace elements in fresh vegetables.     

Comparison of double-pulse and single-pulse laser-induced breakdown spectroscopy techniques in the analysis of powdered samples of silicate raw materials for the brick-and-tile industry

Single- and double-pulse laser-induced breakdown spectroscopy techniques applied to the analysis of pressed pellets of silicate raw materials were compared in terms of precision, sensitivity and limits of detection. Two Nd:YAG lasers (1064 and 532 mm) in an orthogonal configuration with a reheating arrangement have been employed. The main factors influencing system performance were optimized, i.e. laser pulse energies and interpulse separation. The behaviour of plasma temperature was studied over a period of time and calibration curves for Mg were constructed for both the single and double-pulse setup. When comparing the single- and double-pulse techniques, limits of detection of Si and Mg for the double-pulse technique were found to be 10 times lower.     

激光诱导击穿光谱在煤质检测中的应用现状

我国当前主要能源仍是煤炭资源,煤质快速检测有利于其清洁高效利用。激光诱导击穿光谱（Laser-Induced Breakdown Spectroscopy,LIBS）作为一种快速光谱检测技术,具有样品需求量小、制样简便、可多元素同时测量等优点,其在煤质快速检测中的应用潜力已得到广泛认可。本文从激光诱导击穿光谱仪器（实验室台式、在线式和便携式）的研发现状、激光诱导击穿光谱对煤质（金属元素、非金属元素和工业指标）的检测现状、煤质分析性能提升方法,以及激光诱导击穿光谱定量分析模型研究等方面介绍了近几年来LIBS技术在煤质检测中的应用现状及未来展望。     

Filament-induced remote surface ablation for long range laser-induced breakdown spectroscopy operation

We demonstrate laser induced ablation and plasma line emission from a metallic target at distances up to 180 m from the laser, using filaments (self-guided propagation structures ∼ 100 μm in diameter and ∼ 5 × 10¹³ W/cm² in intensity) appearing as femtosecond and terawatt laser pulses propagating in air. The remarkable property of filaments to propagate over a long distance independently of the diffraction limit opens the frontier to long range operation of the laser-induced breakdown spectroscopy technique. We call this special configuration of remote laser-induced breakdown spectroscopy “remote filament-induced breakdown spectroscopy”. Our results show main features of filament-induced ablation on the surface of a metallic sample and associated plasma emission. Our experimental data allow us to estimate requirements for the detection system needed for kilometer-range remote filament-induced breakdown spectroscopy experiment.     

Double-pulse standoff laser-induced breakdown spectroscopy for versatile hazardous materials detection

We have developed a double-pulse standoff laser-induced breakdown spectroscopy (ST-LIBS) system capable of detecting a variety of hazardous materials at tens of meters. The use of a double-pulse laser improves the sensitivity and selectivity of ST-LIBS, especially for the detection of energetic materials. In addition to various metallic and plastic materials, the system has been used to detect bulk explosives RDX and Composition-B, explosive residues, biological species such as the anthrax surrogate Bacillus subtilis, and chemical warfare simulants at 20 m. We have also demonstrated the discrimination of explosive residues from various interferents on an aluminum substrate.     

Probing particle size distributions in natural surface waters from 15 nm to 2 microm by a combination of LIBD and single-particle counting

We present a technique for measuring colloid size distributions between 15 nm and 2 microm at concentrations relevant to natural surface waters. Two particle-measuring methods are combined: laser-induced breakdown detection (LIBD), which allows the quantification of colloid size distributions below 400 nm, and a commercial single-particle counter that extends the accessible size range up to two mum. Centrifugation was used in order to separate micrometer sized particles for the LIBD measurement. The feasibility is demonstrated on water of Lake Brienz (Switzerland) and the River Pfinz (Germany) and the particle size distributions follow Pareto's law even down to 15 nm in both cases.     

Sensitive and selective spectrochemical analysis of metallic samples: the combination of laser-induced breakdown spectroscopy and laser-induced fluorescence spectroscopy

In order to improve on analytical selectivity and sensitivity, the technique of laser-induced fluorescence spectroscopy (LIFS) was combined with laser-induced breakdown spectroscopy (LIBS). The main thrust of this investigation was to address analytical scenarios in which the measurement site may be difficult to access. Hence, a remote LIBS+LIFS arrangement was set up, and the experiments were carried out on samples surrounded by air at atmospheric pressure, rather than in a controlled buffer gas environment at reduced pressure. Representative for proof of principle, the detection of aluminium, chromium, iron and silicon at trace level concentrations was pursued. These elements are of importance in numerous chemical, medical and industrial applications, and they exhibit suitable resonance transitions, accessible by radiation from a pulsed Ti:sapphire laser system (its 2nd and 3rd harmonic outputs). All investigated elements have an energy level structure in which the laser-excited level is a member of a group of closely-spaced energy levels; thus, this allowed for easy off-resonant fluorescence detection (collisional energy transfer processes). Since numerous of the relevant transition wavelengths are within a narrow spectral interval, this opens the possibility for multi-element analysis; this was demonstrated here for Cr and Fe which were accessed by rapidly changing the tuneable laser wavelength.     

Temperature measurements in a decaying laser-induced plasma in air at elevated pressures

This article discusses two measurement techniques for temperature determination of laser-induced plasmas in a gas at pressures relevant for combustion engines. Plasmas induced by laser breakdown in air at initial pressures ranging from 0.3 MPa to 2.5 MPa are investigated using optical spectroscopy. Results for 0.8 MPa, 1.2 MPa and 1.6 MPa are reported here. Due to the elevated pressure, a significant contribution from continuum radiation is apparent. The first temperature measurement technique relies on the interpretation of the continuum emission. The second technique is based on the line emissions from different elements and ionization stages in the plasma and is implemented with the multi-element Saha-Boltzmann plot method. The methodology may be applicable for temperature measurements under various conditions, e.g., for plasmas in high pressure gas environments such as in industrial applications of laser-induced breakdown spectroscopy or for plasma sources for illumination purposes. We investigate optimizations of laser-induced spark ignition. The energy released in the laser-induced plasma is determined based on temperature measurements.