Libs; Soil analysis; Practical powder sample holder; Quantitative powder analysis;ATOMIC EMISSION-SPECTROMETRY; SPECTROCHEMICAL ANALYSIS; PLASMA; LIBS; ABLATION; MATRIX; METALS; PB

A practical alternative of sample preparation technique is proposed for direct powder analysis using laser-induced breakdown spectroscopy (LIBS) instead of the commonly adopted treatment of pelletizing the powder. The resulted pellet is known to suffer from reduced sensitivity of emission. Besides, it may also give rise to interfering effect from the binder emission. We introduce in this report a more practical technique of using a subtarget supported micro mesh (SSMM) powder sample holder. The LIBS spectrum of standard soil powder measured with 13 mJ 1064 nm Nd:YAG laser in 0.65 kPa ambient air is shown to exhibit the sharp emission lines of all the major elements in the sample. A comparison with the emission spectra measured from the pelletized powder, the spectrum obtained using the SSMM sample holder shows distinctly superior spectral quality marked by the absence of matrix effect found in pelletized powder samples, and the much stronger intensity due to the more effective shock wave plasma induced thermal excitation process produced by the hard subtarget in the sample holder. Repeating the measurement on a number of the standard soil samples of various Pb contents is shown to yield a linear calibration line with practically zero intercept and a detection limit of less than 10 ppm. We have thus demonstrated the viability of the proposed powder sample holder for the development of practical and quantitative powder analysis in the field. (C) 2017 Elsevier B.V. All rights reserved.

DUAL-PULSE LIBS; INDUCED PLASMA; ABLATION EFFICIENCY; SENSITIVE ANALYSIS; HELIUM PLASMA; FEMTOSECOND; ENHANCEMENT; NANOSECOND; MICROANALYSIS; DEUTERIUM

A time-resolved spectroscopic study is performed by using 125-500 micro-Joule (mu J) ps laser focused directly without the aid of microscope on a Cu plate sample in a variety of low-pressure ambient gases including air, helium and argon. It is shown that the ultrashort mu J laser-induced low-pressure plasma in Ar ambient gas exhibits the typical characteristics of shock wave plasma responsible for the thermal excitation and sharp emission of the analyte atoms. It is found that the highest signal to background (S/B) ratio of about 100 is achieved in 1.3 kPa argon ambient gas and detected with optical multichannel analyzer (OMA) gate delay of 1 ns and gate width of 50 mu s. The emission spectra obtained from pure Zn sample show the effective suppression of the ionic emission with ablation energy around and below 500 mu J. The experimental setup is successfully applied to Cr analysis with low detection limit in steel. In particular, its application to C analysis in steel is demonstrated to resolve the long standing problem of overlapping contributions from the neutral and ionic Fe emission. It is further found that an element of high excitation energy such as fluorine (F) can be clearly detected from a non metal teflon sample. Further, its application to alluminum sample containing various concentrations of Mg, Ca, Fe, and Si impurity elements clearly displays the existence of linear calibration lines promising for quantitative analyses in certain dynamical ranges. Finally, in view of the tiny crater sizes of less than 10 mu m diameter created by the very low ps laserenergy, this technique is promising for micrometer resolution mapping of elemental distribution on the sample surface and its depth profiling. (C) 2017 The Japan Society of Applied Physics

INDUCED BREAKDOWN SPECTROSCOPY; YAG LASER; EMISSION SPECTROSCOPY; PLANT MATERIALS; HYDROGEN; DEUTERIUM; RESIDUES; ABLATION; NITROGEN

We report the experimental evidence of shock wave plasma generation by direct observation of the plasma propagation using 68 mJ 1064 nm Nd-doped yttrium aluminum garnet laser irradiation on a relatively soft organic sample in He ambient gas at 2 kPa. The density jump associated with the arrival of the plasma front at a certain position is detected by means of the highly sensitive interferometric technique, in conjunction with the observation of the first appearance of the plasma emission at the same position and time of the plasma front arrival. The result shows that the plasma front moves at the Sedov speed, which is typical of shock wave propagation, yielding an excellent emission spectrum for the harder sample. The shock front speed is further found to decrease in the case of a softer sample, resulting in lesser spectroscopic performance, as demonstrated by the emission spectra measured from mochi samples of different hardnesses. The result of this study is promising for paving the way to extending the laser-induced breakdown spectroscopy application to the much needed spectrochemical analysis of agricultural and food products. (c) 2017 Optical Society of America

Trace radioactive pollutant; Cs in water; Cs in soil; Low pressure plasma; ITO film;SHOCK-WAVE PLASMA; SAMPLES; LIBS

An experimental study has been conducted for the practical and in situ application of laser-induced breakdown spectroscopy (LIBS) for the detection of Cs pollutant in water and soil in the nearby area of Fukushima Nuclear Power Station. The spectrochemical measurements were carried out by means of 355 nm Nd-YAG laser with N-2 and He ambient gases at atmospheric and low pressures. The soil samples were prepared by pelletizing the mixtures of 80% soil and 20% KBr while the aqueous samples were prepared as thin films electro deposited on indium tin oxide (ITO) glass. The resulted emission spectra using 0.5 kPa N-2 ambient gas shows the minimum detectable Cs concentration of 0.2 ppm and 0.3 ppm in the water and soil samples, respectively. The result of this experiment has thus demonstrated the viability of the LIBS equipment employed here as a more practical, in-situ and even mobile alternative to the standard use of gamma-ray spectroscopy using germanium detector. (C) 2017 Published by Elsevier B.V.

INDUCED BREAKDOWN SPECTROSCOPY; QUANTITATIVE-ANALYSIS; PULSE; HELIUM; LIBS; CONFIGURATION; MICROANALYSIS; ENHANCEMENT; DEUTERIUM; NM

An experimental study is performed on the time-dependent intensity variations of Zn emission focusing on the triplet (Zn I 481.0 nm) and singlet (Zn I 636.2 nm) emission lines induced under three experimental conditions. A single nanosecond (ns) Nd:YAG laser in standard laser-induced breakdown spectroscopy(LIBS) setup is employed for the investigation of direct shock wave-induced emission characteristics with N-2 ambient gas at 0.4 kPa and the different effects of He ambient gas at 2 kPa. An additional two-laser system consisting of ns and picosecond (ps) lasers in an orthogonal setup is used to study the exclusive role of a He-assisted excitation (HAE) process for the generation of those two Zn emission lines. The results of this study consistently exhibit the dominant triplet emission over the singlet emission marked by initial maximum intensity ratios of 8 and 12 obtained from the experiments using a single-laser setup in N-2 and He ambient gases, respectively, indicating the significant contribution of the HAE mechanism to the enhanced and longer lasting Zn emission in He gas. The experiment using the special two-laser setup further demonstrates the exclusive role of the HAE process in the Zn emission featuring an even markedly higher triplet/singlet intensity ratio of 22. Thus, the results of this study suggest the possibly more general nature of dominant triplet emission phenomena previously found in laser-induced He and Ca emission spectra. (C) 2017 The Japan Society of Applied Physics

DOUBLE-PULSE; QUANTITATIVE-ANALYSIS; INDUCED PLASMA; DEUTERIUM; ABLATION; CHAMBER; GAS

An experimental study is conducted in search of the much needed experimental method for practical and minimally destructive analysis of hydrogen (H) and deuterium (D) in a nuclear power plant. For this purpose, a picosecond (ps) Nd:YAG laser is employed and operated with 300-500 mu J output energies in a variety of ambient gases at various gas pressures. The sample chamber used is specially designed small quartz tube with an open end that can be tightly fitted to the sample surface. It is found that ambient Ar gas at reduced pressure of around 0.13 kPa gives the best spectral quality featuring fully resolved H and D emission lines with clearly detectable intensities and practically free from surface water interference. The D emission intensities measured from zircaloy plates containing various concentrations of D impurity are shown to yield a linear calibration line with extrapolated zero intercept, offering its potential application to quantitative analysis. The estimated detection limit of less than 10 ppm is well below the sensitivity limit of around 600 ppm required for the regular inspection of zircaloy tubes in a heavy water nuclear power plant. The use of the exceedingly low laser energy is shown to offer an additional advantage of minimum destructive effect marked by the resulted tiny craters of about 5 mu m diameter with 25 mu m depth. These results promise the potential development of the desired alternative analytical tool for regular in situ and real time inspection of the zircaloy tubes in a heavy water power plant.

Carbon dioxide laser; heavy metals; laser-induced breakdown spectroscopy; soil;METASTABLE HE ATOMS; SAMPLES; PLASMA; POLLUTION; INPUTS; GAS

A novel method of laser-induced plasma spectroscopy utilizing a pulsed transversely excited atmospheric CO2 laser has been developed for the high-sensitivity determination of heavy metals in soil. A coarse metal powder was used to trap the soil and to assist with plasma generation. When the CO2 laser(10.6 mu m, 1.5J, 200ns) was irradiated on the metal and soil powder, a high-temperature and long-lifetime luminous plasma was induced. Fine particles of soil were dissociated and were excited in the plasma region. The method was used for the rapid determination of Cr, Pb, and Hg in loam. The limits of detection for Cr, Pb, and Hg were approximately 0.8, 15, and 0.7mg/kg, respectively.

laser-induced breakdown spectroscopy; TEA CO2 laser-induced gas plasma; transversely excited atmospheric CO2 laser; powder analysis;INDUCED BREAKDOWN SPECTROSCOPY; SAMPLES; IDENTIFICATION; ABLATION; SOILS

Analysis of powder samples available in small quantities has been carried out using metal-assisted gas plasma by utilizing a transversely excited atmospheric (TEA) CO2 laser. The powder was homogeneously mixed with Si grease, and the mixed powder was painted on a metal subtarget. When a TEA CO2 laserwas directly focused on the metal subtarget at atmospheric pressure of He gas, a high-temperature He gas plasma was induced. It is assumed that the powder particles were vaporized to be effectively atomized and excited in the gas plasma region. This method has been employed in the rapid analyses of elements in organic and inorganic powder samples present in small quantities. Detection of trace elements of Cr and Pb has been successfully made by using the supplement powder and loam soil, respectively. The detection limits of Pb in loam soil were approximately 20 mg/kg.