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1.
A multi-element Saha–Boltzmann plot method is proposed for the determination of the temperature and the relative number density in laser-induced plasmas, assuming local thermodynamic equilibrium and stoichiometry conservation. The method has been applied to the characterization of a plasma generated with a Cu–Fe–Ni–Mn alloy, using a Nd:YAG laser in air at atmospheric pressure. Spectra of the local emissivity have been obtained by spatial deconvolution of the intensity spectra, obtained with spatial resolution. Saha–Boltzmann plots obtained from the emissivities of 58 spectral lines of Fe I, Fe II, Ni I, Ni II, Mn I and Mn II have been fitted to linear behavior with high correlation, which shows the validity of the equation proposed. Radial distributions of the temperature and number densities of neutral atoms and ions have been determined. The results obtained reinforce the initial considerations of local thermodynamic equilibrium and conservation of stoichiometry. The proposed equation can also be applied to only one ionization species (multi-element Boltzmann plot). Spatially-integrated measurements of the plasma emission have also been performed to show that, in this case, the application of the method to the line intensities provides the two different apparent temperatures for neutral atoms and ions. 相似文献
2.
The local values of the parameters that characterize a laser-induced plasma (temperature, electron density, relative number densities of neutral atoms and ions) have been obtained by spatially resolved emission spectroscopy, including the deconvolution of the measured intensity spectra. The plasma has been generated using a Nd:YAG laser with a Fe–Ni alloy in air at atmospheric pressure, and the emission in the time window 3.0–3.5 μs has been detected. The temperature values obtained from neutral atom and ion emissions have been compared in the cases of local and spatially-integrated measurements. Local Boltzmann and Saha–Boltzmann plots with high correlation to linear fittings have been obtained using two broad sets of optically thin neutral atom and ion lines (21 Fe I lines and 15 Fe II lines), resulting in local values of the electronic temperature that coincide within the error. These results of local measurements contrast with those of spatially integrated measurements, for which two different temperatures are obtained from the Boltzmann plots of neutral atoms (9100±150 K) and ions (13 700±300 K). This difference is explained according to the measured distributions of the electronic temperature and the neutral atom and ion number densities, that result in separated emissivity (or population) distributions of neutral atom and ion lines, leading to different neutral atom and ion apparent temperatures (population-averages of the local electronic temperature). Local values of the plasma parameters have been obtained at all the positions with significant emission, including the determination of the electronic temperature from Saha–Boltzmann or Boltzmann plots. The ionization degree is high- and low-varying at the inner part of the plasma, decaying only near the plasma front. The maximum of the ion density does not coincide with the temperature maximum; on the contrary, the axial variation of both the neutral atom and ion densities (that decrease towards the sample surface) is opposite to that of the temperature, a behaviour that is interpreted to result from the plasma expansion process. 相似文献
3.
Measurements of the local electron density in laser-induced plasma have been carried out from the Stark-broadened profiles of three reference lines (Hα, Fe I and Si II). The plasma has been generated from a Fe–Si sample in air using a Nd:YAG laser. Compatible values of the local electron density have been obtained from the three lines. The experiment is based on the use of an imaging spectrometer, the capability for spatial resolution of a charge-coupled device and the application of a spatial deconvolution procedure to the spectra. Distributions of the emission coefficient have been obtained, showing that the three lines are emitted from different regions of the plasma. The implications in the apparent electron density values obtained in spatially-integrated measurements are discussed: similar values are obtained for the Hα and Si II lines, while the Fe I line leads to a 25% lower value. 相似文献
4.
Parametric study of a fiber-optic laser-induced breakdown spectroscopy probe for analysis of aluminum alloys 总被引:2,自引:0,他引:2
Awadhesh K. Rai Hansheng Zhang Fang Yu Yueh Jagdish P. Singh Arel Weisburg 《Spectrochimica Acta Part B: Atomic Spectroscopy》2001,56(12):963-2383
In the present work we demonstrate a fiber-optic laser-induced breakdown spectroscopy (FO LIBS) system for delivering laser energy to a sample surface to produce a spark as well as to collect the resulting radiation from the laser-induced spark. In order to improve the signal/background (S/B) ratio, various experimental parameters, such as laser energy, gate delay and width, detector gain, lenses of different focal lengths and sample surface, were tested. In order to provide high reliability and repeatability in the analysis, we also measured plasma parameters, such as electron density and plasma temperature, and determined their influence on the measurement results. The performance of FO LIBS was also compared with that of a LIBS system that does not use a fiber to transmit the laser beam. LIBS spectra with a good S/B were recorded at 2-μs gate delay and width. LIBS spectra of six different Al alloy samples were recorded to obtain calibration data. We were able to obtain linear calibration data for numerous elements (Cr, Zn, Fe, Ni, Mn, Mg and Cu). A linear calibration curve for LIBS intensity ratio vs. concentration ratio reduces the effect of physical variables (i.e. shot-to-shot power fluctuation, sample-to-surface distance, and physical properties of the samples). Our results reveal that this system may be useful in designing a high-temperature LIBS probe for measuring the elemental composition of Al melt. 相似文献
5.
《Spectrochimica Acta Part B: Atomic Spectroscopy》2006,61(1):69-80
In this work, we have studied the main conditions that a laser-induced plasma must fulfill in order to be considered as adequate for the measurement of Stark broadening parameters. We investigated the effect of the temporal window, the self-absorption, the crater size, and the effect of the spatial inhomogeneity on the emission profiles coming from a laser-induced plasma. Starting from the spatially resolved values of the plasma parameters, obtained by emission spectroscopy, the error in the determination of the Stark electron width due to the spatial inhomogeneity has been estimated and, for the present experimental conditions, was found to be lower than 7%. As a test of the method, the Stark electron broadening constant of Fe I 381.58 nm has been measured using the Fe I 538.34 nm emission line as the reference to determine the electron density. The plasma was produced under a controlled atmosphere of argon at atmospheric pressure, on an iron–nickel alloy sample. The emission was collected by a system with high spectral resolution, for different temporal windows after the laser pulse. For time delays between 2.75 and 21 μs, the electron density showed an evolution in the range 2.0–0.13 × 1017 cm− 3, while the temperature varied from 11 100 to 7100 K. The representation of the Stark electron width of Fe I 381.58 nm, measured for each temporal window, versus the Stark electron width of the reference line showed a linear behavior with a high correlation coefficient. From the slope of this linear fit and the Stark electron broadening constant of the reference line, the Stark width of Fe I 381.58 nm was obtained to be 1.10 ± 0.07 × 10− 2 nm for an electron density of 1017 cm− 3. 相似文献
6.
《Spectrochimica Acta Part B: Atomic Spectroscopy》2003,58(2):221-237
The curves of growth (COG) of five Fe I lines emitted from a laser-induced plasma, generated with Fe–Ni alloys in air at atmospheric pressure, have been investigated. Spectral lines with different energy levels and line widths, emitted with a broad range of optical depths, have been included in the study in order to check the validity of theoretical models proposed for COG generation, based in the radiative transfer within a plasma in local thermodynamic equilibrium. The COGs have been measured at time windows of 4–5 μs and 15–18 μs. The Stark widths of the Fe I lines have been obtained, and the line widths have been determined by measuring the plasma electron density at the time windows selected. It is shown that at a time window of 4–5 μs, the inhomogeneity of the plasma magnitudes has an important influence on the COGs of intense lines. For this time window, a two-region model of the plasma has been used to generate theoretical COGs that describe satisfactorily the experimental curves of all the lines using a single set of plasma parameters. The results reveal the existence of considerable gradients between the inner and the outer plasma regions in the temperature (9400–7800 K) and in the density of Fe atoms (4×1016–0.02×1016 cm−3 for a sample with 100% Fe). On the contrary, at the time window 15–18 μs, at which the plasma has suffered most of its expansion and cooling process, the COGs of all the lines may be described by a single-region model, corresponding to a plasma with uniform temperature (6700 K) and density of Fe atoms (0.06×1016 cm−3 for a sample with 100% Fe). It is also shown that at initial times, the plasma inhomogeneity has an important effect in the line profiles of intense spectral lines, which are described by using the two-region model of the laser-induced plasma. 相似文献
7.
《Spectrochimica Acta Part B: Atomic Spectroscopy》2006,61(2):200-209
We report on recently developed analytical software to model laser-induced breakdown spectroscopy emission spectra and predict sample composition using a proposed calibration-free algorithm. The model uses a database of atomic emission lines to create a theoretical emission spectrum for selected elements using defined plasma parameters. The resulting theoretical spectrum is fitted to experimental data obtained from a laser-induced breakdown spectroscopy instrument comprising of four compact spectrometers that image the plasma emission. Elemental concentrations are obtained by comparing observed and predicted spectra while varying the plasma temperature and relative elemental concentrations. The use of the model for analysis of major elements in bauxites, brass and mineral samples as well as the analysis of laboratory air is demonstrated. For the majority of elements investigated agreement within 25% is achieved between estimated and certified values. 相似文献
8.
Comparison of detection limits, for two metallic matrices, of laser-induced breakdown spectroscopy in the single and double-pulse configurations 总被引:4,自引:0,他引:4
Ismail MA Cristoforetti G Legnaioli S Pardini L Palleschi V Salvetti A Tognoni E Harith MA 《Analytical and bioanalytical chemistry》2006,385(2):316-325
Limits of detection have been studied for several elements in aluminium and steel alloys, at atmospheric pressure in air,
by use of the single and collinear double-pulse configurations of laser-induced breakdown spectroscopy. For this purpose,
calibration plots were constructed for Mg, Al, Si, Ti, Cr, Mn, Fe, Ni, and Cu using a set of certified aluminium alloy samples
and a set of certified steel samples. The investigation included optimization of the experimental conditions to furnish the
best signal-to-noise ratio. Inter-pulse delay, gate width, and acquisition delay were studied. The detection limits for the
elements of interest were calculated under the optimum conditions for the double-pulse configuration and compared with those
obtained under the optimum conditions for single-pulse configuration. Significantly improved detection limits were achieved,
for all the elements investigated, and in both aluminium and steel, by use of the double-pulse configuration. The experimental
findings are discussed in terms of the measured plasma conditions (particle and electron density, and temperature). 相似文献
9.
Cristian A. D'Angelo Diego M. Díaz Pace Graciela Bertuccelli 《Spectrochimica Acta Part B: Atomic Spectroscopy》2009,64(10):999
In this paper, a more realistic approach of a non-uniform optically thick plasma in local thermodynamic equilibrium was applied to describe self-reversal of Co I 340.51 nm emission line recorded from a laser-induced plasma generated on a Co–Cr–Mo metallic alloy. This line was selected because it is one of the most absorbed of the major elements in air at atmospheric pressure.The model describes the behavior of the plasma after the breakdown, and it was semiempirical thus, some information was taken from the experiment. A cylinder-symmetrical plasma column with a parabolic temperature distribution having a maximum at the center and decreasing toward the edges was considered. The input parameters were the plasma length, the temperature in the plasma core, and the Co total density, which were estimated from measurements and previous work. Moreover, the distribution of electron density depended on the temperature, and the ionization degree was taken into account through Saha equation. Then, plasma parameters were adjusted in such a way calculations reproduced the experimentally measured line profiles.The effect of varying laser power on plasma homogeneity and its evolution in time were investigated. Moreover, preliminary results of spatial distribution of plasma parameters were obtained that confirmed the practical application of the model on plasma diagnostics. 相似文献
10.
Kyuseok Song Dukhyeon Kim Hyungki Cha Yonggi Kim Euo Chang Jung Inhee Choi Hee-Soo Yoo Seokwon Oh 《Microchemical Journal》2004,76(1-2):95
An analytical system for simultaneously monitoring laser-ablation mass spectra and laser-induced breakdown spectra for solid sample has been developed. The performance of the developed system is evaluated by measuring characteristics of laser-induced plasma such as lifetime of ions inside the plasma and laser power dependence of mass resolution for solid samples. Adopted samples are gadolinium plate, gadolinium coated on stainless steel plate, and one of the NIST standard samples, C-1248 (Ni–Cu alloy). The threshold laser energy in obtaining mass spectrum was dependent on the type of sample characteristics in the order of a few MW/cm2, while a few hundred MW/cm2 was necessary in order to observe emission signal. When laser energy was increased enough to produce emission signal, mass resolution of the time-of-flight mass spectrum was severely deteriorated. The lifetime of the continuum ion signal was estimated 200 and 250 ns for Gd plate and C-1248, respectively, by monitoring emission signals, while the lifetime of ions near sample surface was estimated as 400 ns and 430 ns for Gd plate and C-1248, respectively. The deterioration of mass resolution can be understood as originating from the space charge effect in high plasma density in a given space and different velocity distribution of ions inside the plasma, while longer lifetime of ions near sample surface can be understood as originating from speed of ion ejection near the sample surface. The details of the characteristics of laser-induced plasma are discussed and optimum experimental conditions for simultaneous monitoring are suggested. 相似文献
11.
Q.L. Ma V. Motto-Ros W.Q. Lei M. Boueri L.J. Zheng H.P. Zeng M. Bar-Matthews A. Ayalon G. Panczer J. Yu 《Spectrochimica Acta Part B: Atomic Spectroscopy》2010
Speleothems represent an important record of the paleoclimate, and more generally past environmental changes thanks to their laminar structure which is related to variations in rainfall and vegetation throughout the seasons and to their elemental as well as structural compositions which are sensitive to climatic and environmental conditions during their growth. Studies of their composition, especially those with spatial resolution, reveal rich information for paleoclimatology. In this paper, we demonstrate that laser-induced breakdown spectroscopy (LIBS) provides a suitable tool for elemental analysis and especially for 2-dimensional elemental mapping of speleothems. Main, minor, as well as trace elements can be analyzed with this technique. The temporal evolution of the induced plasma is first studied in order to determine a suitable detection window for emission spectrum recording following the impact of the laser pulse on the sample. The matrix effect is then evaluated with a scan on the sample surface by measuring the electron density and the temperature of the plasmas at different positions of the analyzed surface. Concentration mapping is performed for minor and trace elements such as Na, Mg, Al, Si, K, Fe and Sr, by measuring relative variations of line emission intensities from these elements. Finally, correlations in concentration among detected elements are determined. Groups of correlated elements can be attributed to different mineralogical phases. 相似文献
12.
A bottleneck of the wide commercial application of laser-induced breakdown spectroscopy (LIBS) technology is its relatively high measurement uncertainty. A partial least squares (PLS) based normalization method was proposed to improve pulse-to-pulse measurement precision for LIBS based on our previous spectrum standardization method. The proposed model utilized multi-line spectral information of the measured element and characterized the signal fluctuations due to the variation of plasma characteristic parameters (plasma temperature, electron number density, and total number density) for signal uncertainty reduction. The model was validated by the application of copper concentration prediction in 29 brass alloy samples. The results demonstrated an improvement on both measurement precision and accuracy over the generally applied normalization as well as our previously proposed simplified spectrum standardization method. The average relative standard deviation (RSD), average of the standard error (error bar), the coefficient of determination (R2), the root-mean-square error of prediction (RMSEP), and average value of the maximum relative error (MRE) were 1.80%, 0.23%, 0.992, 1.30%, and 5.23%, respectively, while those for the generally applied spectral area normalization were 3.72%, 0.71%, 0.973, 1.98%, and 14.92%, respectively. 相似文献
13.
To further develop laser-induced breakdown spectroscopy (LIBS) as an analytical technique, it is necessary to better understand the fundamental processes and mechanisms taking place during the plasma evolution. This paper addresses the very early plasma dynamics (first 100 ns) using direct plasma imaging, light scattering, and transmission measurements from a synchronized 532-nm probe laser pulse. During the first 50 ns following breakdown, significant Thomson scattering was observed while the probe laser interacted with the laser-induced plasma. The Thomson scattering was observed to peak 15–25 ns following plasma initiation and then decay rapidly, thereby revealing the highly transient nature of the free electron density and plasma equilibrium immediately following breakdown. Such an intense free electron density gradient is suggestive of a non-equilibrium, free electron wave generated by the initial breakdown and growth processes. Additional probe beam transmission measurements and electron density measurements via Stark broadening of the 500.1-nm nitrogen ion line corroborate the Thomson scattering observations. In concert, the data support the finding of a highly transient plasma that deviates from local thermodynamic equilibrium (LTE) conditions during the first tens of nanoseconds of plasma lifetime. The implications of this early plasma transient behavior are discussed in the context of plasma–analyte interactions and the role on LIBS measurements. 相似文献
14.
采用扫描电子显微镜-X射线能谱(SEM-EDS)及电感耦合等离子体发射光谱(ICP-OES)法对锂离子电池用镍钴锰酸锂中镍、钴、锰三元素间的摩尔比进行了测定。结果显示,在SEM-EDS测定过程中,如果将样品压成片状,选择合理的测定电压,同时对镍、钴谱线的重叠峰进行分峰拟合,以独立正态分布峰的面积换算各元素的摩尔百分比,SEM-EDS的测定结果与ICP-OES的测定结果具有较高的一致性,二者相对偏差不大于5%。镍、钴、锰三元素摩尔比的SEM-EDS测量值的相对标准偏差(n=3)不大于1%。 相似文献
15.
S. Beldjilali D. Borivent L. Mercadier E. Mothe G. Clair J. Hermann 《Spectrochimica Acta Part B: Atomic Spectroscopy》2010
We have performed spectroscopic analysis of the plasma generated by Nd:YAG laser irradiation of flesh and skin of fresh potatoes. From the spectra recorded with an Echelle spectrometer 11 minor elements have been identified. Their relative concentrations were estimated by comparing the measured spectra to the spectral radiance computed for a plasma in local thermal equilibrium. According the moderate plasma temperature of about 6500 K at the time of spectroscopic observation, the electrons are essentially generated by the ionization of the minor metal atoms, making plasma modeling possible although the organic elements may be out of equilibrium. Among the spectral lines selected for the analysis, the Na I 588.99 and 589.59 nm doublet was found to be partially self-absorbed allowing us to estimate the number density of sodium atoms. The value was found to agree with the number density predicted by the plasma model. As a result, the relative concentrations of the detected minor elements have been estimated for both the flesh and skin of the potatoes. Among these, aluminum and silicon were found to have relatively large mass fractions in the potato skin whereas their presence was not detected in the flesh. The present study shows that laser-induced breakdown spectroscopy is a promising tool to measure the elemental composition of fresh vegetables without any sample preparation. 相似文献
16.
17.
《Spectrochimica Acta Part B: Atomic Spectroscopy》2005,60(2):215-230
A radiation dynamic model of the postbreakdown stage of laser-induced plasma solves a twofold task: first, the direct problem, it yields an analytical expression for the plasma radiation dynamics under arbitrarily chosen initial conditions allowing the computation of synthetic spectra; second, the inverse problem, it allows finding of the initial conditions by a direct comparison of calculated synthetic spectra with experimentally measured ones. In this work, we carry out experimental verification of the model, thus dealing with the inverse problem. We vary the initial parameters of the model (plasma initial temperature and the initial concentrations of species) until a close fit between the synthetic and the experimental spectrum is obtained. Some of the model inputs (e.g., the initial radius of the plasma) are measured and introduced into the model as fixed constants. Calculations and measurements are performed on a binary SiC system; on a series of multicomponent aluminum samples doped with Si, Mg, Cu, Zn, and Fe; and on pure iron, silicon, and carbon. From two to six elements and up to 500 spectral lines were involved in the calculations. The Monte Carlo optimization (the simulated annealing method) is used for finding initial plasma temperature and number densities. A reasonably good agreement is obtained between the computed and the experimental spectra. This approach can be considered as a valuable step towards the achievement of absolute analysis. 相似文献
18.
Masaki Ohata Hiroyuki Yasuda Yoshimichi Namai Naoki Furuta 《Analytical sciences》2002,18(10):1105-1110
The source of signal variations that governs the analytical performance of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) was investigated in this study. In order to specify the source of signal variations of LA-ICP-MS, laser-induced plasma (LIP) Fe emission, LA-ICP-MS Fe+ and LA-ICP-MS Ni+ signals were used as internal standards for the determination of trace elements in low-alloy steel certified reference materials (BS 50D and JSS 1005-1008). Fe 1373.5 nm emission signals from LIP were measured, while trace element LA-ICP-MS signals were collected. After that, the LIP emission signals, LA-ICP-MS Fe+ and LA-ICP-MS Ni+ signals were used as internal standards, and the analytical performance was evaluated by the RSDs and the correlation coefficients (r) of the calibration curves. The improvement factors were dependent on the internal standardization methods. Analytical precisions (RSDs) of trace element LA-ICP-MS signals were improved by factors of 1.5-3.3 using LIP Fe emission signals as an internal standard. The improvement factors of 2.5 - 5.9 and 4.1 - 17 were obtained by using LA-ICP-MS Fe+ and LA-ICP-MS Ni+ signals as internal standards, respectively. Better correlation coefficients (r) were also obtained using the LA-ICP-MS signal compensation (0.9985 by LA-ICP-MS Fe+ and 0.9996 by LA-ICP-MS Ni+) rather than the LIP Fe emission compensation (0.9932). In this paper we compare and discuss the analytical performance achieved by LA-ICP-MS using LIP Fe emission, LA-ICP-MS Fe+ and LA-ICP-MS Ni+ signals as internal standards. 相似文献
19.
Time and spacially resolved spectra of a cylindrically symmetric exploding thin film plasma were obtained with a rotating mirror camera and astigmatic imaging. These spectra were decouvolved to obtain relative spectral emissivity profiles for nine Fe(II) and two Fe(I) lines. The effective (electronic) excitation temperature at various positions in the plasma and at various times during the first current halfcycle was computed from the Fe(II) emissivity values using the Boltzmann graphical method. The Fe(II)/Fe(I) emissivity ratios together with the temperature were used to determine the degree of ionization of Fe. Finally, the electron density was estimated from the Saha equilibrium. Electronic excitation temperatures range from 10,000–15,000 K near the electrode surface at peak discharge current to 7000–10,000 K at 6–10 mm above the electrode surface at the first current zero. Corresponding electron densities range from 1017-1018 cm?3 at peak current to 1015-1016cm?3 near zero current. Error propagation and criteria for thermodynamic equilibrium are discussed. 相似文献
20.
Christopher Brian Dreyer Greg S. Mungas Phihung Thanh Juliez George Radziszewski 《Spectrochimica Acta Part B: Atomic Spectroscopy》2007,62(12):1448-1459
Laser-Induced Breakdown Spectroscopy (LIBS) and Raman spectroscopy are complimentary techniques. LIBS yields elemental information while Raman spectroscopy yields molecular information about a sample, and both share similar instrumentation configurations. The combination of LIBS and Raman spectroscopy in a single instrument for planetary surface exploration has been proposed, however challenges exist for developing a combined instrument. We present LIBS and Raman spectroscopy results obtained using a diode pumped, intracavity doubled, Q-switched, Nd:YLF laser operating at 523 nm, which overcomes some of the difficulties associated with a combined instrument. LIBS spectra were obtained with 170 μJ per pulse at 4 Hz repetition rate in a low pressure Mars-simulated atmosphere and Raman spectra produced with 200 mW at 100 kHz. The Nd:YLF laser is switchable between LIBS and Raman spectroscopy modes only by a change in Q-switch repetition rate. Emissions from Ca, Ca II, Fe, Fe II, Mg, Na, and O atom were identified in the μ-LIBS spectrum of oolithic hematite. Evidence was found for a change in plasma dynamics between 7 and 5 Torr that could be explained as a decrease in plasma temperature and electron density below 5 Torr. This is relevant to future Mars exploration using LIBS as the mean surface pressure on Mars varies from 3.75 to 6 Torr. LIBS plasma dynamics should be carefully evaluated at the pressures that will be encountered at the specific Mars landing site. 相似文献