Simultaneous determination of traces in solid samples with laser-AAS

Microamounts of solid samples are vaporized by focused laser radiation (Q-switch ruby). The solid aerosol is transported in an Ar gas stream to a hot graphite tube. The determination of trace metals is made by flameless AAS.A dual channel AA spectrometer is used for the investigation of the reproducibility of the absorbance values in indirect laser AAS. The simultaneous determination of Ag-Mn an Pb-Ag in copper standard metals and in pellets of organic powders show that the inhomogeneity of the materials and differences in the material vaporization by the laser light influence the analytical results.The results of the simultaneous determination of Ag, Al, Mn, Ni. and Pb in different solid samples are compared mutually and with the results of flameless AAS determinations of solutions.     

Multilayer adsorption equilibrium model for gas adsorption on solids

Adaptation of the ENSIC model to physisorption of nitrogen or argon on a solid surface first led to a 3 parameters model called multilayer adsorption equilibrium model (MAE model). One of these parameters is related to the formation of a multilayer of adsorbate on the solid surface. Exploitation of data from the literature pointed out that this parameter does not depend on the nature of the solid surface and an average value was calculated in the case of N₂ and Ar. As a consequence, the MAE model can be considered as a 2 parameters model. Linearization of the model was established allowing an easy determination of surface areas of macroporous and some mesoporous solids. Fitting of isotherms of meso and macroporous solids has led to promising results compared to the ones obtained with the BET model. Moreover, adaptation of this model to microporous solids can also be used for an uncomplicated determination of porous volume and external surface. Results obtained from data of the literature were close to those obtained with the t-plot model.     

Photo- and thermally stimulated relaxation processes in pre-irradiated atomic solids

Atomic and electronic relaxation processes in pre-irradiated atomic solids are considered using preliminary irradiated by an electron beam solid Ar as an example. The results of real-time-correlated study are presented for the first time with an accent on recently found anomalous low-temperature sputtering of Ar atoms from the surface. The experiments were performed using a set of activation spectroscopy methods—thermally stimulated exoelectron emission (TSEE) thermally stimulated luminescence (TSL) in combination with measurements of the sputtering yield. Solid evidence of thermally induced charge recombination mechanism is obtained. Mechanism of energy transfer based on the crowdion model is discussed. Photo-stimulated sputtering from pre-irradiated rare gas solids (RGS) is predicted.     

Direct Determination of Copper in Solids and Ores by Laser Ablation-Direct Current Argon Plasma Emission Spectrometry

Abstract

The use of a laser ablation-direct current argon plasma emission spectrometric system for the direct determination of metals in solids is described. Sample preparation of solid steel samples involves machining to fit the geometry of the ablation chamber. A cellulose binder and copper ore are mixed thoroughly in a ball mill to ensure homogeneity and pelletized in a press at 20000 psi to fit the geometry of the ablation chamber. Copper, manganese, and nickel are determined using the system on standard steel samples, and copper is determined in pelletized copper ore with good agreement obtained with certified values. Precisions are typically in the 3 - 10% range with a detectable limit of 100 μg g^?1 of copper.     

Direct Determination of Aluminum in Archaeological Clays by Laser‐Induced Breakdown Spectroscopy

Abstract

Instrumental techniques that allow the direct analysis of solids with little or no sample preparation are particularly important for the evaluation of samples that are difficult to analyze such as refractory or geological materials. Laser‐induced breakdown spectroscopy (LIBS) is a promising technique for the direct, rapid analysis of elements in solid materials with minimal sample preparation. The main advantages over wet techniques are virtual nondestructiveness and analysis speed. The goal of this work is the direct determination of aluminum of archaeological pieces using laser‐induced breakdown spectroscopy. The corresponding signals of metals were interpolated from calibration graphs of different salts of the metals. The matrix effects from the direct determination of these elements were thoroughly investigated. The potential of this technique for direct quantitative analysis of real archaeological materials (from Department of Ancient Science, University of Zaragoza) was evaluated, and the reproducibility of LIBS spectra from different archaeological samples was measured as a function of the number of laser shots. Finally, the results from LIBS are compared with those obtained by laser ablation inductively coupled plasma mass spectrometry.     

Recent trends and developments in laser ablation-ICP-mass spectrometry

The increased interest in laser technology (e.g. for micro-machining, for medical applications, light shows, CD-players) is a tremendous driving force for the development of new laser types and optical set-ups. This directly influences their use in analytical chemistry. For direct analysis of the elemental composition of solids, mostly solid state lasers, such as Nd:YAG laser systems operating at 1064 nm (fundamental wavelength), 266 nm (frequency quadrupled) and even 213 nm (frequency quintupled) have been investigated in combination with all available inductively coupled plasma mass spectrometers. The trend towards shorter wavelengths (1064 nm - 157 nm) was initiated by access to high quality optical materials which led to the incorporation of UV gas lasers, such as excimer lasers (XeCl 308 nm, KrF 248 nm, ArF 193 nm, and F2 157 nm) into laser ablation set-ups. The flexibility in laser wavelengths, output energy, repetition rate, and spatial resolution allows qualitative and quantitative local and bulk elemental analysis as well as the determination of isotope ratios. However, the ablation process and the ablation behavior of various solid samples are different and no laser wavelength was found suitable for all types of solid samples. This article highlights some of the successfully applied systems in LA-ICP-MS. The current fields of applications are explained on selected examples using 266 nm and 193 nm laser ablation systems.     

Intracavity laser atomic absorption spectrometry with graphite furnace atomizer or pulsed laser sampler

An absorption intracavity laser spectrometer with two types of sample vaporization systems (graphite furnace electrothermal atomizer or laser sampler) is described that can be used for the determination of trace amounts of metals (Al, Cr, Fe and Mn) in liquid samples and at the surface of solid targets. The limits of detection for the elements tested are lower than those obtained by modern conventional spectrometers. The examined technique provides a wide dynamic range of linear standard calibration curves.     

Intracavity laser atomic absorption spectrometry with graphite furnace atomizer or pulsed laser sampler

An absorption intracavity laser spectrometer with two types of sample vaporization systems (graphite furnace electrothermal atomizer or laser sampler) is described that can be used for the determination of trace amounts of metals (Al, Cr, Fe and Mn) in liquid samples and at the surface of solid targets. The limits of detection for the elements tested are lower than those obtained by modern conventional spectrometers. The examined technique provides a wide dynamic range of linear standard calibration curves.     

Recent trends and developments in laser ablation-ICP-mass spectrometry

The increased interest in laser technology (e.g. for micro-machining, for medical applications, light shows, CD-players) is a tremendous driving force for the development of new laser types and optical set-ups. This directly influences their use in analytical chemistry. For direct analysis of the elemental composition of solids, mostly solid state lasers, such as Nd:YAG laser systems operating at 1064 nm (fundamental wavelength), 266 nm (frequency quadrupled) and even 213 nm (frequency quintupled) have been investigated in combination with all available inductively coupled plasma mass spectrometers. The trend towards shorter wavelengths (1064 nm– 157 nm) was initiated by access to high quality optical materials which led to the incorporation of UV gas lasers, such as excimer lasers (XeCl 308 nm, KrF 248 nm, ArF 193 nm, and F₂ 157 nm) into laser ablation set-ups. The flexibility in laser wavelengths, output energy, repetition rate, and spatial resolution allows qualitative and quantitative local and bulk elemental analysis as well as the determination of isotope ratios. However, the ablation process and the ablation behavior of various solid samples are different and no laser wavelength was found suitable for all types of solid samples. This article highlights some of the successfully applied systems in LA-ICP-MS. The current fields of applications are explained on selected examples using 266 nm and 193 nm laser ablation systems.     

The absorption and excitation spectroscopy of matrix-isolated atomic manganese: sites of isolation in the solid rare gases

This study collects information from absorption and luminescence excitation spectra recorded for Mn atoms isolated in the solid rare gases Ar, Kr, and Xe and presents an analysis of the site occupancy, based on the polarizabilities of the rare gases and the observed spectral shifts. Two thermally stable sites of isolation exist for atomic Mn in solid Ar and Kr, while a single thermally stable site is present in Mn/Xe. Site occupancy assignments are based on the application of a polarizability model to the z (6)P(5/2)<--a (6)S(5/2); z (8)P(5/2)<--a (6)S(5/2), and y (6)P(5/2)<--a (6)S(5/2) electronic transitions of atomic Mn. From an analysis of the observed RG matrix-to-gas phase energy shifts for P<--S type transitions, this model allows the association of certain site types occupied by metal atoms in the rare gas solids. The required condition being a linear dependence of the matrix shifts with rare gas polarizability for those metal atoms "trapped" in a particular site type. Application of the polarizability model in conjunction with trends observed in site dominance, established a connection between the blue sites in Ar and Kr and the single site in Xe. Use of the known MgRG ground state bond lengths facilitated an identification of the sites of Mn atom isolation assuming the transference of the known MgRG bond lengths to the MnRG systems. Substitutional site occupancy of atomic Mn is assigned to the blue sites in Ar and Kr and the single site in Xe, while tetra-vacancy site occupancy is assigned to the red sites in Ar and Kr. Consistent with these assignments, Mn atoms in solid Ar show a preference for trapping in tetra-vacancy sites whereas in solid Kr, single substitutional sites are preferred and in Xe, this is the only site observed.     

A method for determining argon isotopes in a continuous helium flow for K/Ar geochronology

A new method for the measurement of the argon isotope composition in a continuous helium flow using isotope mass spectrometers is described for potassium-argon geochronology. Argon was extracted from the samples in a chamber with a multiple-sample holder by successively heating the samples with a continuous infrared laser. Argon extracted in the chamber was preconcentrated in a capillary, separated on a chromatographic capillary column in a helium flow, and then injected into the ion source of a mass spectrometer through an open splitter. Measurements of the ³⁶Ar, ³⁸Ar, and ⁴⁰Ar isotopes were carried out on isotope mass spectrometers in a dynamic mode using a triple-collector ion detector and three electrometric amplifiers. Preliminary experiments on the developed device for measuring argon isotopes in a continuous helium flow have shown that the proposed method can be used for the determination of radiogenic argon in an amount of n × 10^?12 g with the accuracy satisfying the solution of many geochronological problems. In sensitivity and reproducibility, the proposed method is highly competitive to the isotope dilution method for measuring argon and simpler than the conventional methods for measuring radiogenic argon.     

Studies of LA-ICP-MS on quartz glasses at different wavelengths of a Nd:YAG laser

The capability of LA-ICP-MS for determination of trace impurities in transparent quartz glasses was investigated. Due to low or completely lacking absorption of laser radiation, laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) proves difficult on transparent solids, and in particular the quantification of measurement results is problematic in these circumstances. Quartz glass reference materials of various compositions were studied by using a Nd:YAG laser system with focused laser radiation of wavelengths of 1064 nm, 532 nm and 266 nm, and an ICP-QMS (Elan 6000, Perkin Elmer). The influence of ICP and laser ablation conditions in the analysis of quartz glasses of different compositions was investigated, with the laser power density in the region of interaction between laser radiation and solid surface determining the ablation process. The trace element concentration was determined via calibration curves recorded with the aid of quartz glass reference materials. Under optimized measuring conditions the correlation coefficients of the calibration curves are in the range of 0.9–1. The relative sensitivity factors of the trace elements determined in the quartz glass matrix are 0.1–10 for most of the trace elements studied by LA-ICP-MS. The detection limits of the trace elements in quartz glass are in the low ng/g to pg/g range.     

Studies of LA-ICP-MS on quartz glasses at different wavelengths of a Nd:YAG laser

The capability of LA-ICP-MS for determination of trace impurities in transparent quartz glasses was investigated. Due to low or completely lacking absorption of laser radiation, laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) proves difficult on transparent solids, and in particular the quantification of measurement results is problematic in these circumstances. Quartz glass reference materials of various compositions were studied by using a Nd:YAG laser system with focused laser radiation of wavelengths of 1064 nm, 532 nm and 266 nm, and an ICP-QMS (Elan 6000, Perkin Elmer). The influence of ICP and laser ablation conditions in the analysis of quartz glasses of different compositions was investigated, with the laser power density in the region of interaction between laser radiation and solid surface determining the ablation process. The trace element concentration was determined via calibration curves recorded with the aid of quartz glass reference materials. Under optimized measuring conditions the correlation coefficients of the calibration curves are in the range of 0.9-1. The relative sensitivity factors of the trace elements determined in the quartz glass matrix are 0.1-10 for most of the trace elements studied by LA-ICP-MS. The detection limits of the trace elements in quartz glass are in the low ng/g to pg/g range.     

On-line double isotope dilution laser ablation inductively coupled plasma mass spectrometry for the quantitative analysis of solid materials

We report on the determination of trace elements in solid samples by the combination of on-line double isotope dilution and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). The proposed method requires the sequential analysis of the sample and a certified natural abundance standard by on-line IDMS using the same isotopically-enriched spike solution. In this way, the mass fraction of the analyte in the sample can be directly referred to the certified standard so the previous characterization of the spike solution is not required. To validate the procedure, Sr, Rb and Pb were determined in certified reference materials with different matrices, including silicate glasses (SRM 610, 612 and 614) and powdered samples (PACS-2, SRM 2710a, SRM 1944, SRM 2702 and SRM 2780). The analysis of powdered samples was carried out both by the preparation of pressed pellets and by lithium borate fusion. Experimental results for the analysis of powdered samples were in agreement with the certified values for all materials. Relative standard deviations in the range of 6–21% for pressed pellets and 3–21% for fused solids were obtained from n = 3 independent measurements. Minimal sample preparation, data treatment and consumption of the isotopically-enriched isotopes are the main advantages of the method over previously reported approaches.     

Direct determination of cadmium in solids using a capacitively coupled microwave plasma atomic emission spectrometer

A capacitively coupled microwave plasma (CMP) operating at 800 W was examined for the direct determination of cadmium in solids. The laboratory-constructed system contained a tungsten cup electrode capable of holding microsample quantities. A low-powered plasma was used to heat the sample, while at higher powers the plasma was used for sample vaporization and excitation. This plasma enabled thermal vaporization (TV) sample introduction to be accomplished in situ as the plasma formed directly around the sample. Thus, the need for sample preparation, procedural steps and sample transport was eliminated. This technique was capable of the direct determination of trace elements in solid samples in less than 5 min. The effects of experimental parameters such as gas flow rate, atomization power and electrode position were investigated. Detection limits obtained for Cd by TV-CMP-AES were in the picogram range with a relative standard deviation of <20%. The accuracy and precision of the method were also evaluated by measuring Cd in several NIST Standard Reference Materials.     

Laser-induced ablation of a steel sample in different ambient gases by use of collinear multiple laser pulses

The sensitivity of laser-induced breakdown spectroscopy of solid samples depends on the number of ablated and excited analytes. Laser ablation of solid samples can be enhanced by using collinear multiple laser pulses, for example double or triple pulses, rather than single laser pulses with the same total laser pulse energy. The ablation rates and the plasma conditions are affected by the ambient gas. In this study laser ablation was examined by varying the interpulse separation of the multiple pulses, within double and triple-pulse bursts, and the gas mass density at constant gas pressure. Different ambient gases and gas mixtures consisting of argon, oxygen, and nitrogen were used to study their effect on ablation rates. In a pure argon atmosphere (99.999% v/v Ar) the ablation burst number required to penetrate a steel plate of thickness 100 μm is reduced by a factor of approximately six by use of triple-pulse bursts with a symmetric interpulse separation of 15 μs rather than single pulses with the same total burst energy of 105 mJ. For double and single pulses the factors are 1.6 for Ar and 2.8 for synthetic air. Analyte lines are 4 to 8 times more intense if an argon atmosphere, rather than air, is used.     

On-line microwave-assisted digestion of solid samples for their flame atomic spectrometric analysis

A new procedure has been developed for the on-line digestion of solids in a microwave oven. The direct injection in a water carrier flow of dispersions of solid samples in concentrated nitric acid, the merging of these slurries with 30% (v/v) H(2)O(2) and the microwave-assisted digestion in a Teflon coil of 100 cm permit a fast and quantitative extraction of Cu and Mn from different solid matrices, such as vegetables, powdered dietary products and sewage sludges. The development of an appropriate interphase, in which digested samples are cooled and degassified, previous to their introduction into the nebulizer of a flame atomic absorption spectrometer, makes possible the full automatization of the digestion and measurement steps of the elemental analysis of solids and it provides a sample frequency of 180 injections per hour. The developed procedure has also been applied for Pb and Zn determination in certified sewage sludge samples, with accurate results obtained for Pb but low results found for Zn.     

IR spectra of CH3F in liquid and solid noble gas solutions

The IR absorption spectra of CH3F doped Ar, Kr and Xe solutions have been recorded near the melting point. The full widths at half maximum of fundamental bands increase noticeably after crystallization of the Xe and Kr solutions. A slight narrowing of the bands is observed just below the freezing point of the Ar solution. Treated in the framework of the Debye model for the J-diffusion of a symmetric top rotation, the results suggest a weaker perturbation of rotational motion of CH3F in the ordered Xe and Kr solids at least near the freezing point. At the same time, molecular rotation becomes more hindered when going to solid Ar. The broadening effect has been found to correlate with a hopping increase of the vibrational energy relaxation time, measured by the IR-IR double resonance method.     

Novel multichannel plasma-source mass spectrometer

A novel mass spectrometer system for elemental analysis is described. The instrument combines an inductively coupled plasma (ICP) ion source with a Mattauch-Herzog mass spectrometer and multichannel ion detector. Ion detection is simultaneous and an elemental mass spectrum (20–230 μ) can be acquired in <10 ms. The instrument can be used with either Ar or He plasma sources. The speed of the system makes it well suited for acquisition of fast (10–100-ms duration) transient signals, such as those generated by pulsed laser ablation sample introduction. Preliminary system performance characteristics, which include detection limits, stability, and measurement accuracy, obtained with an Ar ICP are presented. The application of the instrument to the analysis of solid samples by laser ablation is discussed.     

Measuring polarizability anisotropies of rare gas diatomic molecules by laser-induced molecular alignment technique

The polarizability anisotropies of homonuclear rare gas diatomic molecules, Ar(2), Kr(2), and Xe(2), are investigated by utilizing the interaction of the induced electric dipole moment with a nonresonant, nanosecond laser pulse. The degree of alignment, which depends on the depth of the interaction potential created by the intense laser field, is measured, and is found to increase in order of Ar(2), Kr(2), and Xe(2) at the same peak intensity. Compared with a reference I(2) molecule, Ar(2), Kr(2), and Xe(2) are found to have the polarizability anisotropies of 0.45 ± 0.13, 0.72 ± 0.13, and 1.23 ± 0.21 A?(3), respectively, where the uncertainties (one standard deviation) in the polarizability anisotropies are carefully evaluated on the basis of the laser intensity dependence of the degree of alignment. The obtained values are compared with recent theoretical calculations and are found to agree well within the experimental uncertainties.