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Sample records for plasma-optical emission spectroscopy

  1. Inductively coupled plasma optical emission spectroscopy determination of trace element composition of argan oil.

    Science.gov (United States)

    Gonzálvez, A; Ghanjaoui, M E; El Rhazi, M; de la Guardia, M

    2010-02-01

    A methodology based on inductively coupled plasma optical emission spectroscopy (ICP-OES) after microwave assisted acid digestion has been developed to determine the trace element content of Moroccan argan oil. Limit of detection values equal or lower than few mg/kg were obtained for all elements under study. To assure the accuracy of the whole procedure, recovery studies were carried out on argan oil samples spiked at different concentration levels from 10 to 200 µg/L. Quantitative average recovery values were obtained for all elements evaluated, demonstrating the suitability of this methodology for the determination of trace elements in argan oil samples. Aluminum, calcium, chromium, iron, potassium, lithium, magnesium, sodium, vanadium and zinc were quantitatively determined in Moroccan argan oils being found that their concentration is different of that found in other edible oils thus offering a way for authentication and for the evaluation of possible adulterations.

  2. Copper Determination in Gunshot Residue by Cyclic Voltammetric and Inductive Coupled Plasma-Optical Emission Spectroscopy

    Directory of Open Access Journals (Sweden)

    Mohd Hashim Nurul’Afiqah Hashimah

    2016-01-01

    Full Text Available Analysis of gunshot residue (GSR is a crucial evidences for a forensic analyst in the fastest way. GSR analysis insists a suitable method provides a relatively simple, rapid and precise information on the spot at the crime scene. Therefore, the analysis of Cu(II in GSR using cyclic voltammetry (CV on screen printed carbon electrode (SPCE is a better choice compared to previous alternative methods such as Inductive Coupled Plasma-Optical Emission Spectroscopy (ICP-OES those required a long time for analysis. SPCE is specially designed to handle with microvolumes of sample such as GSR sample. It gives advantages for identification of copper in GSR on-site preliminary test to prevent the sample loss on the process to be analyzed in the laboratory. SPCE was swabbed directly on the shooter’s arm immediately after firing and acetate buffer was dropped on SPCE before CV analysis. For ICP-OES analysis, cotton that had been soaked in 0.5 M nitric acid was swabbed on the shooter’s arm immediately after firing and kept in a tightly closed sampling tube. Gold coated SPCE that had been through nanoparticles modification exhibits excellent performance on voltammograms. The calibration was linear from 1 to 50 ppm of copper, the limit of detection for copper was 0.3 ppm and a relative standard deviation was 6.1 %. The method was successfully applied to the determination of copper in GSR. The Cu determination on SPCE was compared and validated by ICP-OES method with 94 % accuracy.

  3. Inductively Coupled Plasma Optical-Emission Spectroscopy Determination of Major and Minor Elements in Vinegar

    Directory of Open Access Journals (Sweden)

    Arzu AKPINAR-BAYIZIT

    2010-12-01

    Full Text Available This study characterizes the mineral content of vinegar samples. The concentrations of Na, K, Ca, Mg and P (major elements as well as Fe, Mn, Sn, Cu, Ni, Zn, Pb and Cd (minor elements were determined in 35 commercial vinegar samples using inductively coupled plasma optical-emission spectrometry (ICP-OES. The elements with the highest concentrations were K, Na, Ca, Mg and P. The concentrations of heavy metals in the vinegar samples, including Cd, Ni, Sn and Pb, were not considered a health risk.

  4. Determination of Silicon in Gasoline by Directly Measuring under Organic Phase Using Inductively Coupled Plasma Optical Emission Spectroscopy.

    Science.gov (United States)

    Zhang, Wen-mei; Wen, Huan; Lü, Huan-ming; Liu, Hui-qin; Lin, Zhi-sheng; Wang, Rong-hua

    2015-03-01

    A simple and accurate method was developed for determining silicon in gasoline using inductively coupled plasma optical emission spectroscopy (ICP-OES). For sample inroduction a Burgener nubulizer and a Cyclonic spray chamber were used. A gasoline sample was diluted with isooctane and then introduced into the cooled spray chamber of the ICP-OES. Good linearity was achieved in the silicon concentration range 0.1 - 10.0 mg x kg(-1), and the correlation coefficient was 0.999 96. The detection limit for silicon was 0.012 mg x kg(-1) and the silicon recoveries from gasoline samples were 95.8% - 98.4%, with relative standard deviations of less than 3.0% The method was proved to be simple, reliable and highly sensitive, and suitable for determining silicon in samples of motor gasoline, ethanol-gasoline and methanol-gasoline fuel mixtures those containing not more than 15% (V/V) oxygenates.

  5. Laser Induced Breakdown Spectroscopy compared with conventional plasma optical emission techniques for the analysis of metals - A review of applications and analytical performance

    Science.gov (United States)

    Bengtson, A.

    2017-08-01

    This review is focused on a comparison of LIBS with the two most common plasma Optical Emission Spectroscopy (OES) techniques for analysis of metals; spark OES and glow discharge (GD) OES. It is shown that these two techniques have only minor differences in analytical performance. An important part of the paper reviews a direct comparison of the analytical figures of merit for bulk analysis of steels using spark and LIBS sources. The comparison was carried out using one instrument with interchangeable sources, eliminating differences related to the optical system and detectors. It was found that the spark provides slightly better analytical figures of merit. The spark analysis is considerably faster, the simple design of the spark stand has enabled complete automation, both properties of great importance in the metallurgical industry for routine analysis. The analysis of non-metallic inclusions (NMI) with spark and LIBS is presented, in the case of the spark this has become known as Pulse Distribution Analysis (PDA). A very significant difference between the techniques is that the electrical spark typically evaporates 100 times more material than a single laser pulse, resulting in complete evaporation of an NMI present in the evaporated metal. The major advantage of LIBS is that it is localised with very good lateral resolution. The major advantages of spark is that it is much faster (can be done simultaneous with the bulk analysis) and easier to quantify. Compositional Depth Profiling (CDP) is compared for GD-OES and LIBS. It is shown that for applications where GD-OES is well suited, e.g. coated metallic sheet, GD-OES still performs slightly better than LIBS. Similar to the case of NMI analysis, the major advantage of LIBS is the great lateral resolution. This allows elemental surface mapping, as well as CDP of very small areas on μm scale. One further advantage of LIBS is that samples of almost any material, shape and size can be analysed, whereas GD-OES has

  6. Environmental biomonitoring of essential and toxic elements in human scalp hair using accelerated microwave-assisted sample digestion and inductively coupled plasma optical emission spectroscopy.

    Science.gov (United States)

    Kumakli, Hope; Duncan, A'ja V; McDaniel, Kiara; Mehari, Tsdale F; Stephenson, Jamira; Maple, Lareisha; Crawford, Zaria; Macemore, Calvin L; Babyak, Carol M; Fakayode, Sayo O

    2017-05-01

    Human scalp hair samples were collected and used to assess exposure to toxic elements and essential elements in the state of North Carolina, USA using accelerated microwave assisted acid digestion and inductively coupled plasma optical emission spectroscopy (ICP-OES). The figures-of-merit of the ICP-OES were appropriate for elemental analysis in scalp hair with detection limits as low as 0.0001 mg/L for Cd, good linearity (R(2) > 0.9978), and percent recoveries that ranged from 96 to 106% for laboratory-fortified-blanks and 88-112% for sample spike recovery study. The concentrations of essential elements in scalp hair were larger than those of toxic elements, with Ca having the highest average concentration (3080 μg/g, s = 14,500, n = 194). Some of the maximum concentrations observed for As (65 μg/g), Ni (331 μg/g), Cd (2.96 μg/g), and Cr (84.6 μg/g) in individual samples were concerning, however. Samples were statistically analyzed to determine the influence of race, gender, smoking habits, or age on the elemental concentrations in scalp hair. Higher concentrations of essential elements were observed in the scalp hair of Caucasians, females, and non-smokers, and the differences were often significant at a 90% confidence level. Several pairs of essential elements, for example Ca-K, Ca-Mg, and Ca-Zn, were strongly correlated in Caucasian hair but uncorrelated in African-American hair. Similarly, essential elements were strongly correlated in female hair but weakly correlated in male hair. Toxic element pairs (As-Cd, As-Se, Pb-As, and Se-Cd) were strongly correlated in the hair of smokers but uncorrelated in that of non-smokers, suggesting that cigarette smoke is a common source of toxic elements in humans. Published by Elsevier Ltd.

  7. Analysis of cobalt, tantalum, titanium, vanadium and chromium in tungsten carbide by inductively coupled plasma-optical emission spectrometry

    CSIR Research Space (South Africa)

    Archer, M

    2003-12-01

    Full Text Available Inductively coupled plasma optical emission spectroscopy (ICP-OES) was used to measure the concentrations of cobalt, tantalum, titanium, vanadium and chromium in solutions of tungsten carbide. The main advantage of the method described here lies...

  8. Evaluation of conductive polymers as an adsorbent for eradication of As (III from aqueous solution using inductively coupled plasma optical emission spectroscopy (ICP-OES

    Directory of Open Access Journals (Sweden)

    Muhammad Imran Din

    2014-04-01

    Full Text Available 1024x768 The main focused of this research work is the preparation of conductive polymers like polypyrrole, polyaniline and polythiophene and their application as adsorbent materials for the removal of hyper toxic metal As (III from aqueous solution. The metal ions get attached on the π-electrons at the back bone of polymer that illustrate excellent affinity for metal ions. The adsorption of As (II ions was carried out on polythiophene due to its redox properties and the stronger interaction between sulfur atoms with arsenic atoms. To attain large surface area and for maximum interaction of As (III ions with polymers, the particle size of polymers was ranged in nano scale. As the surface area increases with decrease in particle size, the active sites for metal ions also increases. These polymers were characterized by FIIR spectroscopy and SEM analysis. Adsorption isothermal data was examined by two parameters (Langmuir, Freundlich, and Dubinin-Radushkevich and three parameters Redlich-Petrson, Sips and Toth models. Experimental results showed that based on standard deviation (SD and Chi square test (χ2 the experimental data was best explained by Freundlich and Toth isotherm. Thermodynamics parameters such as free energy change (ΔG0, enthalpy change (ΔH0 and entropy change (ΔS0 have been calculated respectively, which revealed the spontaneous, endothermic and feasible nature of adsorption process.   Normal 0 false false false EN-US X-NONE X-NONE

  9. Tandem Laser Induced Breakdown Spectroscopy (LIBS), Laser Ablation Inductively Coupled Plasma Mass Spectroscopy (LA-ICP-MS) and/or Laser Ablation Inductively Coupled Plasma Optical Emission Spectroscopy (LA-ICP-OES) for the analysis of samples of geological interest

    Science.gov (United States)

    Oropeza, D.

    2016-12-01

    A highly innovative laser ablation sampling instrument (J200 Tandem LA - LIBS) that combines the capabilities and analytical benefits of LIBS, LA-ICP-MS and LA-ICP-OES was used for micrometer-scale, spatially-resolved, elemental analysis of a wide variety of samples of geological interest. Data collected using ablation systems consisted of nanosecond (Nd:YAG operated 266nm) and femtosecond lasers (1030 and 343nm). An ICCD LIBS detector and Quadrupole based mass spectrometer were selected for LIBS and ICP-MS detection, respectively. This tandem instrument allows simultaneous determination of major and minor elements (for example, Si, Ca, Na, and Al, and trace elements such as Li, Ce, Cr, Sr, Y, Zn, Zr among others). The research also focused on elemental mapping and calibration strategies, specifically the use of emission and mass spectra for multivariate data analysis. Partial Least Square Regression (PLSR) is shown to minimize and compensate for matrix effects in the emission and mass spectra improving quantitative analysis by LIBS and LA-ICP-MS, respectively. The study provides a benchmark to evaluate analytical results for more complex geological sample matrices.

  10. Laser ablation inductively coupled plasma optical emission spectrometry for analysis of pellets of plant materials

    Energy Technology Data Exchange (ETDEWEB)

    Gomes, Marcos S. [Departamento de Química, Universidade Federal de São Carlos, Rod. Washington Luís, km 235, 13565-905 São Carlos, SP (Brazil); Centro de Energia Nuclear na Agricultura, Universidade de São Paulo, Av. Centenário 303, 13416-000 Piracicaba, SP (Brazil); Schenk, Emily R. [Department of Chemistry and Biochemistry, Florida International University, Miami, FL (United States); International Forensic Research Institute, Florida International University, Miami, FL (United States); Santos, Dário [Departamento de Ciências Exatas e da Terra, Universidade Federal de São Paulo, Rua Professor Arthur Riedel 275, Diadema, SP (Brazil); Krug, Francisco José [Centro de Energia Nuclear na Agricultura, Universidade de São Paulo, Av. Centenário 303, 13416-000 Piracicaba, SP (Brazil); Almirall, José R., E-mail: almirall@fiu.edu [Department of Chemistry and Biochemistry, Florida International University, Miami, FL (United States); International Forensic Research Institute, Florida International University, Miami, FL (United States)

    2014-04-01

    An evaluation of laser ablation inductively coupled plasma optical emission spectroscopy (LAICP OES) for the direct analysis of pelleted plant material is reported. Ground leaves of orange citrus, soy and sugarcane were comminuted using a high-speed ball mill, pressed into pellets and sampled directly with laser ablation and analyzed by ICP OES. The limits of detection (LODs) for the method ranged from as low as 0.1 mg kg{sup −1} for Zn to as high as 94 mg kg{sup −1} for K but were generally below 6 mg kg{sup −1} for most of the elements of interest. A certified reference material consisting of a similar matrix (NIST SRM 1547 peach leaves) was used to check the accuracy of the calibration and the reported method resulted in an average bias of ∼ 5% for all the elements of interest. The precision for the reported method ranged from as low as 4% relative standard deviation (RSD) for Mn to as high as 17% RSD for Zn but averaged ∼ 6.5% RSD for all the elements (n = 10). The proposed method was tested for the determination of Ca, Mg, P, K, Fe, Mn, Zn and B, and the results were in good agreement with those obtained for the corresponding acid digests by ICP-OES, no differences being observed by applying a paired t-test at the 95% confidence level. The reported direct solid sampling method provides a fast alternative to acid digestion that results in similar and appropriate analytical figures of merit with regard to sensitivity, accuracy and precision for plant material analysis. - Highlights: • An evaluation of LA-ICP-OES for the direct analysis of pelleted plant material is reported. • Orange citrus, soy and sugarcane plants were pressed into pellets and sampled directly. • The element menu consisted of Ca, Mg, P, K, Fe, Mn, Zn and B. • LODs for the method ranged from 0.1 mg kg{sup −1} for Zn to 94 mg kg{sup −1} for K. • The precision ranged from 4% RSD for Mn to 17% RSD for Zn (∼ 6.5% RSD average)

  11. Multi-elemental analysis of aqueous geological samples by inductively coupled plasma-optical emission spectrometry

    Science.gov (United States)

    Todorov, Todor I.; Wolf, Ruth E.; Adams, Monique

    2014-01-01

    Typically, 27 major, minor, and trace elements are determined in natural waters, acid mine drainage, extraction fluids, and leachates of geological and environmental samples by inductively coupled plasma-optical emission spectrometry (ICP-OES). At the discretion of the analyst, additional elements may be determined after suitable method modifications and performance data are established. Samples are preserved in 1–2 percent nitric acid (HNO3) at sample collection or as soon as possible after collection. The aqueous samples are aspirated into the ICP-OES discharge, where the elemental emission signals are measured simultaneously for 27 elements. Calibration is performed with a series of matrix-matched, multi-element solution standards.

  12. Trace elemental composition of curry by inductively coupled plasma optical emission spectrometry (ICP-OES).

    Science.gov (United States)

    Gonzálvez, A; Armenta, S; De La Guardia, M

    2008-01-01

    A methodology based on inductively coupled plasma optical emission spectrometry (ICP-OES) after microwave-assisted acid digestion was developed to determine the content of traces elements in curry samples from the Spanish market. The methodology was validated in terms of accuracy by the analysis of citrus and tomato leaf reference materials achieving comparable results with the certified values. The trace metal content of curry samples was compared with data available from previously published reports concerning Indian samples, especially in terms of heavy metal composition, in order to guarantee the quality of the commercially available spices in the European countries. Values found for the analysis of arsenic, lead and cadmium were significantly lower than the maximum limit allowed by European Union statutory limits for heavy metals and lower than those obtained for Indian curry leaves reported by Indian research teams by using neutron activation and γ-ray analysis.

  13. Oxygen bomb combustion of biological samples for inductively coupled plasma optical emission spectrometry

    Science.gov (United States)

    Souza, Gilberto B.; Carrilho, Elma Neide V. M.; Oliveira, Camila V.; Nogueira, Ana Rita A.; Nóbrega, Joaquim A.

    2002-12-01

    A rapid sample preparation method is proposed for decomposition of milk powder, corn bran, bovine and fish tissues, containing certified contents of the analytes. The procedure involves sample combustion in a commercial stainless steel oxygen bomb operating at 25 bar. Most of the samples were decomposed within 5 min. Diluted nitric acid or water-soluble tertiary amines 10% v/v were used as absorption solutions. Calcium, Cu, K, Mg, Na, P, S and Zn were recovered with the bomb washings and determined by inductively coupled plasma optical emission spectrometry (ICP-OES). Ethanol mixed with paraffin was used as a combustion aid to allow complete combustion. A cooling step prior releasing of the bomb valve was employed to increase the efficiency of sample combustion. Iodine was also determined in milk samples spiked with potassium iodide to evaluate the volatilization and collection of iodine in amine CFA-C medium and the feasibility of its determination by ICP-OES with axial view configuration. Most of the element recoveries in the samples were between 91 and 105% and the certified and found contents exhibited a fair agreement at a 95% confidence level.

  14. Multielemental inductively coupled plasma optical emission spectrometry analysis of nickeliferous minerals.

    Science.gov (United States)

    Abad-Peña, Elizabet; Larrea-Marín, María Teresa; Villanueva-Tagle, Margarita Edelia; Pomares-Alfonso, Mario Simeón

    2014-06-01

    An inductively coupled plasma optical emission spectrometry method for the quantitative simultaneous determination of Al, Ca, Co, Cu, Cr, Fe, K, Mg, Mn, Na, Ni, P and Zn in Cuban laterite and serpentine minerals has been developed. Additionally, V and Ti can be quantitatively determined in laterite mineral; Li, Sr, and Zr can be detected in both mineral types and Pb can be detected just in laterite mineral. The microwave-assisted total acid digestion of samples was achieved with HCl+HNO3+HF and HNO3+HClO4+HF acid mixtures for laterite and serpentine samples, respectively. In non-robust plasma operating conditions, the matrix effect characteristics of the laterite sample were dictated by the principal component Fe; while the character of the Mg principal component matrix effect was some how modified by the concomitants Fe and Ni in serpentine sample. The selection of robust conditions decreased the matrix effect. Additionally, the simulation of the matrix samples by introducing the principal component Fe or Mg, correspondingly, in calibration dissolutions was needed to overcome completely the matrix effect over the analysis accuracy. Precision of analysis was very near or lower than 10% for most elements, except Sr (15%) in L-1; and K (15%) and Li (15%) in SNi sample. Accuracy of analysis was around or lowers than 10% for most elements, except K (15%), Na (19%), P (19%) and V (19%) in L-1 sample; and Ca (14%) and P (20%) in SNi sample. Copyright © 2014 Elsevier B.V. All rights reserved.

  15. Direct determination of sulfur species in coals from the Argonne premium sample program by solid sampling electrothermal vaporization inductively coupled plasma optical emission spectrometry.

    Science.gov (United States)

    Bauer, Daniela; Vogt, Thomas; Klinger, Mathias; Masset, Patrick Joseph; Otto, Matthias

    2014-10-21

    A new direct solid sampling method for speciation of sulfur in coals by electrothermal vaporization inductively coupled plasma optical emission spectrometry (ETV-ICP OES) is presented. On the basis of the controlled thermal decomposition of coal in an argon atmosphere, it is possible to determine the different sulfur species in addition to elemental sulfur in coals. For the assignment of the obtained peaks from the sulfur transient emission signal, several analytical techniques (reflected light microscopy, scanning electron microscopy with energy dispersive X-ray spectroscopy and X-ray diffraction) were used. The developed direct solid sampling method enables a good accuracy (relative standard deviation ≤ 6%), precision and was applied to determine the sulfur forms in the Argonne premium coals, varying in rank. The generated method is time- and cost-effective and well suited for the fast characterization of sulfur species in coal. It can be automated to a large extent and is applicable for process-accompanying analyses.

  16. Development of a direct hydride generation nebulizer for the determination of selenium by inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Carrion, Nereida E-mail: ncarrion@strix.ciens.ucv.ve; Murillo, Miguel; Montiel, Edie; Diaz, Dorfe

    2003-08-15

    A study was conducted to evaluate the performance of a new direct hydride generation nebulizer system for determination of hydride forming elements by inductively coupled plasma optical emission spectroscopy. This system was designed and optimized to obtain the highest sensitivity. Several experimental designs were used for these purposes. To optimize the individual parameters of the system, and to study the interaction between these parameters for both direct hydride generation nebulizers, a central composite orthogonal design with eight factors was set up. Significant behavioral differences were observed in the two direct hydride generation nebulizers studied. Finally, a 70 {mu}m gas orifice nebulizer exhibits a better detection limit than the 120 {mu}m nebulizer. Generally, for determination of selenium, this new direct hydride generation nebulizer system exhibits a linear dynamic range and detection limit (3{sigma}b) of 3 orders of magnitude and 0.2 {mu}g l{sup -1} for selenium, respectively. This new hydride generator is much simpler system that conventional hydride generation systems, which does not need to be changed to work in normal mode with the inductively coupled plasma, since this system may be used for hydride forming elements and those that do not form them. It produces a rapid response with low memory effect. It reduces the interference level of Ni, Co and Cu to 600, 500 and 5 mg l{sup -1}, respectively. The accuracy of the system was verified by the determination of selenium in several standard reference materials of ambient, food and clinical sample matrices. No statistically significant differences (95 confidence level) were obtained between our method and the reference values.

  17. Uncertainty Estimation of Metals and Semimetals Determination in Wastewater by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES)

    Science.gov (United States)

    Marques, J. R.; Villa-Soares, S. M.; Stellato, T. B.; Silva, T. B. S. C.; Faustino, M. G.; Monteiro, L. R.; Pires, M. A. F.; Cotrim, M. E. B.

    2016-07-01

    The measurement uncertainty is a parameter that represents the dispersion of the results obtained by a method of analysis. The estimation of measurement uncertainty in the determination of metals and semimetals is important to compare the results with limits defined by environmental legislation and conclude if the analytes are meeting the requirements. Therefore, the aim of this paper is present all the steps followed to estimate the uncertainty of the determination of amount of metals and semimetals in wastewater by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). Measurement uncertainty obtained was between 4.6 and 12.2% in the concentration range of mg.L-1.

  18. Simultaneous determination of macronutrients, micronutrients and trace elements in mineral fertilizers by inductively coupled plasma optical emission spectrometry

    Science.gov (United States)

    de Oliveira Souza, Sidnei; da Costa, Silvânio Silvério Lopes; Santos, Dayane Melo; dos Santos Pinto, Jéssica; Garcia, Carlos Alexandre Borges; Alves, José do Patrocínio Hora; Araujo, Rennan Geovanny Oliveira

    2014-06-01

    An analytical method for simultaneous determination of macronutrients (Ca, Mg, Na and P), micronutrients (Cu, Fe, Mn and Zn) and trace elements (Al, As, Cd, Pb and V) in mineral fertilizers was optimized. Two-level full factorial design was applied to evaluate the optimal proportions of reagents used in the sample digestion on hot plate. A Doehlert design for two variables was used to evaluate the operating conditions of the inductively coupled plasma optical emission spectrometer in order to accomplish the simultaneous determination of the analyte concentrations. The limits of quantification (LOQs) ranged from 2.0 mg kg- 1 for Mn to 77.3 mg kg- 1 for P. The accuracy and precision of the proposed method were evaluated by analysis of standard reference materials (SRMs) of Western phosphate rock (NIST 694), Florida phosphate rock (NIST 120C) and Trace elements in multi-nutrient fertilizer (NIST 695), considered to be adequate for simultaneous determination. Twenty-one samples of mineral fertilizers collected in Sergipe State, Brazil, were analyzed. For all samples, the As, Ca, Cd and Pb concentrations were below the LOQ values of the analytical method. For As, Cd and Pb the obtained LOQ values were below the maximum limit allowed by the Brazilian Ministry of Agriculture, Livestock and Food Supply (Ministério da Agricultura, Pecuária e Abastecimento - MAPA). The optimized method presented good accuracy and was effectively applied to quantitative simultaneous determination of the analytes in mineral fertilizers by inductively coupled plasma optical emission spectrometry (ICP OES).

  19. Liquid electrode plasma-optical emission spectrometry combined with solid-phase preconcentration for on-site analysis of lead.

    Science.gov (United States)

    Barua, Suman; Rahman, Ismail M M; Alam, Iftakharul; Miyaguchi, Maho; Sawai, Hikaru; Maki, Teruya; Hasegawa, Hiroshi

    2017-08-15

    A relatively rapid and precise method is presented for the determination of lead in aqueous matrix. The method consists of analyte quantitation using the liquid electrode plasma-optical emission spectrometry (LEP-OES) coupled with selective separation/preconcentration by solid-phase extraction (SPE). The impact of operating variables on the retention of lead in SPEs such as pH, flow rate of the sample solution; type, volume, flow rate of the eluent; and matrix effects were investigated. Selective SPE-separation/preconcentration minimized the interfering effect due to manganese in solution and limitations in lead-detection in low-concentration samples by LEP-OES. The LEP-OES operating parameters such as the electrical conductivity of sample solution; applied voltage; on-time, off-time, pulse count for applied voltage; number of measurements; and matrix effects have also been optimized to obtain a distinct peak for the lead at λmax=405.8nm. The limit of detection (3σ) and the limit of quantification (10σ) for lead determination using the technique were found as 1.9 and 6.5ng mL(-1), respectively. The precision, as relative standard deviation, was lower than 5% at 0.1μg mL(-1) Pb, and the preconcentration factor was found to be 187. The proposed method was applied to the analysis of lead contents in the natural aqueous matrix (recovery rate:>95%). The method accuracy was verified using certified reference material of wastewaters: SPS-WW1 and ERM-CA713. The results from LEP-OES were in good agreement with inductively coupled plasma optical emission spectrometry measurements of the same samples. The application of the method is rapid (≤5min, without preconcentration) with a reliable detection limit at trace levels. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. Simultaneous determination of macronutrients, micronutrients and trace elements in mineral fertilizers by inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira Souza, Sidnei de [Laboratório de Química Analítica Ambiental (LQA), Departamento de Química, Centro de Ciências Exatas e Tecnologia, Universidade Federal de Sergipe (UFS), 49100-000, São Cristovão, SE (Brazil); Silvério Lopes da Costa, Silvânio [Laboratório de Química Analítica Ambiental (LQA), Departamento de Química, Centro de Ciências Exatas e Tecnologia, Universidade Federal de Sergipe (UFS), 49100-000, São Cristovão, SE (Brazil); Coordenação de Química, Universidade Federal de Alagoas (UFAL), Campus Arapiraca, 57309-005, Arapiraca, AL (Brazil); Santos, Dayane Melo; Santos Pinto, Jéssica dos; Garcia, Carlos Alexandre Borges [Laboratório de Química Analítica Ambiental (LQA), Departamento de Química, Centro de Ciências Exatas e Tecnologia, Universidade Federal de Sergipe (UFS), 49100-000, São Cristovão, SE (Brazil); and others

    2014-06-01

    An analytical method for simultaneous determination of macronutrients (Ca, Mg, Na and P), micronutrients (Cu, Fe, Mn and Zn) and trace elements (Al, As, Cd, Pb and V) in mineral fertilizers was optimized. Two-level full factorial design was applied to evaluate the optimal proportions of reagents used in the sample digestion on hot plate. A Doehlert design for two variables was used to evaluate the operating conditions of the inductively coupled plasma optical emission spectrometer in order to accomplish the simultaneous determination of the analyte concentrations. The limits of quantification (LOQs) ranged from 2.0 mg kg{sup −1} for Mn to 77.3 mg kg{sup −1} for P. The accuracy and precision of the proposed method were evaluated by analysis of standard reference materials (SRMs) of Western phosphate rock (NIST 694), Florida phosphate rock (NIST 120C) and Trace elements in multi-nutrient fertilizer (NIST 695), considered to be adequate for simultaneous determination. Twenty-one samples of mineral fertilizers collected in Sergipe State, Brazil, were analyzed. For all samples, the As, Ca, Cd and Pb concentrations were below the LOQ values of the analytical method. For As, Cd and Pb the obtained LOQ values were below the maximum limit allowed by the Brazilian Ministry of Agriculture, Livestock and Food Supply (Ministério da Agricultura, Pecuária e Abastecimento — MAPA). The optimized method presented good accuracy and was effectively applied to quantitative simultaneous determination of the analytes in mineral fertilizers by inductively coupled plasma optical emission spectrometry (ICP OES). - Highlights: • Determination of inorganic constituents in mineral fertilizers was proposed. • Experimental design methodology was used to optimize analytical method. • The sample preparation procedure using diluted reagents (HNO{sub 3} and H{sub 2}O{sub 2}) was employed. • The analytical method was satisfactorily to the determination of thirteen elements. • The

  1. Potential of Solid Sampling Electrothermal Vaporization for solving spectral interference in Inductively Coupled Plasma Optical Emission Spectrometry

    Science.gov (United States)

    Asfaw, Alemayehu; Wibetoe, Grethe

    2009-05-01

    Spectral interference is one of the main causes of erroneous results in Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). This paper describes some cases of spectral interferences with conventional nebulization ICP-OES and the potential of solving them utilizing electrothermal vaporization for volatility-based separation. The cases studied were, the well-known spectral overlap between the As and Cd lines at 228.8 nm that are only 10 pm apart, and the interference of Fe on the main emission lines of As, Cd and Pb. The spectral interferences were studied by monitoring the typical signals of solutions that contain the analytes and the potential interferent, by studying the spectra and calculating Background Equivalent Concentration (BEC)-values. A three step temperature program was developed to be used for direct analysis of solid soil samples by Electrothermal Vaporization (ETV)-ICP-OES: step 1 (760 °C, 40 s), step 2 (1620 °C, 20 s) and a cleaning step (2250 °C, 10 s) where Cd vaporizes in step 1, As, Pb and part of Fe in step 2 and the major part of Fe in the cleaning step. Because As and Cd were time-separated using this program, their prominent lines at 228.8 nm, could be used for determination of each element by ETV-ICP-OES, in spite of the serious wavelength overlap. Selective vaporization was also shown to reduce or eliminate the Fe background emission on As, Cd and Pb lines. To confirm the applicability of the method, a solid soil certified reference materials was analyzed directly without any sample treatment. Good or reasonable accuracy was obtained for the three elements.

  2. On-line system for preconcentration and determination of metals in vegetables by Inductively Coupled Plasma Optical Emission Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Bezerra, Marcos A. [Universidade Federal da Bahia, Instituto de Quimica, Grupo de Pesquisa em Quimica Analitica, Campus Universitario de Ondina, Salvador, Bahia 40170-290 (Brazil); Universidade Estadual do Sudoeste da Bahia, Laboratorio de Quimica Analitica, Campus de Jequie, Jequie, Bahia 45206-190 (Brazil); Santos, Walter N.L. dos [Departamento de Ciencias Exatas e da Terra, Universidade do Estado da Bahia, R. Silveira Martins, 2555, Salvador, Bahia 41195-001 (Brazil); Lemos, Valfredo A. [Universidade Estadual do Sudoeste da Bahia, Laboratorio de Quimica Analitica, Campus de Jequie, Jequie, Bahia 45206-190 (Brazil)], E-mail: vlemos@uesb.br; Korn, Maria das Gracas A.; Ferreira, Sergio L.C. [Universidade Federal da Bahia, Instituto de Quimica, Grupo de Pesquisa em Quimica Analitica, Campus Universitario de Ondina, Salvador, Bahia 40170-290 (Brazil)

    2007-09-05

    A procedure has been developed for the simultaneous determination of trace amounts of cadmium, copper, chromium, nickel and lead in digested vegetable samples. The method involves solid-phase extraction of the metals using a minicolumn of Amberlite XAD-4 modified with dihydroxybenzoic acid (DHB) and detection by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). The elution of the metals from minicolumn was performed with 1.0 mol L{sup -1} hydrochloric acid. Variables associated with flow preconcentration system performance, such as pH, buffer concentration, eluent concentration and sampling flow rate, were optimized. The developed procedure provides enrichment factors of 100, 72, 16, 91 and 53, for cadmium, copper, chromium, nickel and lead, respectively. Detection limits (3{sigma}{sub B}) were 0.02 (Cd), 0.23 (Cu), 0.58 (Cr), 0.060 (Ni) and 0.54 (Pb) {mu}g L{sup -1}. The procedure was applied for determination of metals in samples of guarana and cabbage. The accuracy of the method was checked by the analysis of a certified reference material (NIST 1571, Orchard leaves). Results found were in agreement with certified values.

  3. Possibilities of High Resolution Inductively Coupled Plasma Optical Emission Spectrometry in the Determination of Trace Elements in Environmental Materials

    Directory of Open Access Journals (Sweden)

    Nikolaya Velitchkova

    2013-01-01

    Full Text Available This paper presents new quantitative data for the spectral interferences obtained by high resolution 40.68 MHz radial viewing inductively coupled plasma optical emission spectrometry (HR-ICP-OES in the determination of Zn, Cd, Sb, Cu, Mn, Pb, Sn, Cr, U, and Ba in environmental materials in the presence of a complex matrix, containing Al, Ca, Fe, Mg, and Ti. The -concept for quantification of spectral interferences was used. The optimum line selection for trace analysis of a variety of multicomponent matrices requires the choice of prominent lines, which are free or negligibly influenced by line interference problems. The versatility of -concept as basic methodology was experimentally demonstrated in the determination of trace of elements in soil and drinking water. The detection limits are lower in comparison with corresponding threshold concentration levels for soil and drinking water in accordance with environmental regulations. This paper shows the possibilities of present day ICP-OES equipment in the direct determination of trace elements (without preconcentration of impurities in environmental samples.

  4. Solid-Sampling Electrothermal Vaporization Inductively Coupled Plasma Optical Emission Spectrometry for Direct Determination of Total Oxygen in Coal.

    Science.gov (United States)

    Vogt, Thomas; Bauer, Daniela; Nennstiel, David; Otto, Matthias

    2015-10-20

    A new analytical method for direct determination of total oxygen contents in eight coal samples of the Argonne Premium Coal (APC) series and in the NIST SRM 1632d is presented. The development of a suitable calibration procedure, optimization of measurement conditions, and the application of a tailored data processing for handling of plasma effects and high blanks enable the quantification of oxygen simultaneously with other trace, minor, or major elements in whole coal samples by means of electrothermal vaporization inductively coupled plasma optical emission spectrometry (ETV-ICP OES). For comparison, the oxygen contents were determined by a direct oxygen analyzer. The obtained oxygen values of the APC and the reference material NIST SRM 1632d were compared to data in the literature. The precision of the ETV-ICP OES was within ±3.5%, and the recovery better than 92%. With this good accuracy, the developed direct solid sampling method ETV-ICP OES is well suited for the fast determination of oxygen in coals, varying in rank from lignite to semianthracite, in a content range of about 100 ppm up to 27% using 1.5 mg sample weight. This direct analysis method represents an accurate, advantageous alternative to currently used methods for estimation of total oxygen contents in coals.

  5. Evaluation of the mineral profile of textile materials using inductively coupled plasma optical emission spectrometry and chemometrics

    Energy Technology Data Exchange (ETDEWEB)

    Menezes, E.A.; Carapelli, R.; Bianchi, S.R. [Grupo de Analise Instrumental Aplicada, Departamento de Quimica, Universidade Federal de Sao Carlos, Sao Carlos, SP (Brazil); Embrapa Pecuaria Sudeste, C.P. 339, Sao Carlos, SP 13560-970 (Brazil); Souza, S.N.P. [Grupo de Analise Instrumental Aplicada, Departamento de Quimica, Universidade Federal de Sao Carlos, Sao Carlos, SP (Brazil); Matos, W.O. [Departamento de Quimica Analitica e Fisico-Quimica, Universidade Federal do Ceara, Fortaleza, CE (Brazil); Pereira-Filho, E.R. [Grupo de Analise Instrumental Aplicada, Departamento de Quimica, Universidade Federal de Sao Carlos, Sao Carlos, SP (Brazil); Nogueira, A.R.A., E-mail: anarita@cppse.embrapa.br [Embrapa Pecuaria Sudeste, C.P. 339, Sao Carlos, SP 13560-970 (Brazil)

    2010-10-15

    The content of Al, Ba, Ca, Cr, Cu, Fe, Ni, P, Zn, Cd and Pb was determined in textile material samples after microwave-assisted decomposition in a cavity oven and extraction with an artificial sweat solution. Radial viewing inductively coupled plasma optical emission spectrometry (ICP OES) was the main detection technique, but Cd and Pb were determined by thermospray flame furnace atomic absorption spectrometry (TS-FF-AAS) to increase the sensitivity. Principal components analysis (PCA) was applied to the data sets to characterize the samples with respect to their geographic origin and color difference. The PCA for Brazilian single-color samples showed separation, with one group consisting of blue and green textiles and another with all the other materials evaluated. The geographic origin study showed a clear separation between Brazilian and Chinese textiles. The metals amount extracted with sweat extractable solution were lower than limits values pointed by the International Testing and Certification System for Textiles, Oko Tex Standard 100, in the all considered classes. Recoveries varied from 85 to 112% for additions ranging from 3.0 to 25 mg kg{sup -1} for Ca and from 0.3 to 7.0 mg kg{sup -1} for all other analytes through the microwave-assisted decomposition procedure.

  6. Direct determination of impurities in high purity silicon carbide by inductively coupled plasma optical emission spectrometry using slurry nebulization technique.

    Science.gov (United States)

    Wang, Zheng; Qiu, Deren; Ni, Zheming; Tao, Guangyi; Yang, Pengyuan

    2006-09-08

    A novel method for the determination of Al, Ca, Cr, Cu, Fe, Mg, Mn, Ni and Ti in high purity silicon carbide (SiC) using slurry introduction axial viewed inductively coupled plasma optical emission spectrometry (ICP-OES) was described. The various sizes of SiC slurry were dispersed by adding dispersant polyethylene imine (PEI). The stability of slurry was characterized by zeta potential measurement, SEM observation and signal stability testing. The optimal concentration of PEI was found to be 0.5 wt% for the SiC slurry. Analytical results of sub-mum size SiC by the slurry introduction were in good accordance with those by the alkaline fusion method which verified that determination could be calibrated by aqueous standards. For mum size SiC, results of most elements have a negative deviation and should be calibrated by the Certified Reference Material slurry. Owing to a rather low contamination in the sample preparation and stability of the slurry, the limits of detection (LODs), which are in the range of 40-2000 ng g(-1), superior to those of the conventional nebulization technique by ICP-OES or ICP-MS.

  7. Dispersive liquid–liquid microextraction combined with laser-induced breakdown spectrometry and inductively coupled plasma optical emission spectrometry to elemental analysis

    OpenAIRE

    Gaubeur, Ivanise; Aguirre Pastor, Miguel Ángel; Kovachev, Nikolay; Hidalgo Núñez, Montserrat; Canals Hernández, Antonio

    2015-01-01

    In this paper, two analytical methodologies based on the combination of dispersive liquid–liquid microextraction with inductively coupled plasma optical emission spectrometry and laser-induced breakdown spectrometry, respectively, were evaluated for simultaneous preconcentration and detection of Cd, Co, Ni, Pb and Zn. The microextraction procedure was based on the injection of appropriate quantities of 1-undecanol and methanol into the sample solution containing the complexes formed between m...

  8. Aerosol generation of As and Se hydrides using a new Flow Blurring® multiple nebulizer for sample introduction in inductively coupled plasma optical emission spectrometry

    OpenAIRE

    Pereira, Catarinie D.; Aguirre Pastor, Miguel Ángel; NÓBREGA, Joaquim A.; Hidalgo Núñez, Montserrat; Canals Hernández, Antonio

    2014-01-01

    A new Flow Blurring® multiple nebulizer (FBMN) has been used for the efficient generation of As and Se hydrides directly into the aerosol formed inside the spray chamber before detection by inductively coupled plasma optical emission spectrometry (ICP OES). The FBMN allowed the hydride generation directly into the spray chamber without using any additional device either for solution and gas control or for gas phase separation. Synthetic solutions containing As and Se plus Ca, Mg and K were us...

  9. The determination of trace element concentrations in fly ash samples using ultrasound-assisted digestion followed with inductively coupled plasma optical emission spectrometry

    OpenAIRE

    Ilander, Aki; Väisänen, Ari

    2009-01-01

    A method of ultrasound-assisted digestion followed by inductively coupled plasma optical emission spectrometry (ICP-OES) used for the determination of trace element (chromium, copper, lead, nickel, vanadium and zinc) concentrations in fly ash samples was developed. All the measurements were performed in robust plasma conditions. Ultrasound-assisted digestion procedures using digestion solutions of aqua regia and hydrofluoric acid (HF) resulted in recovery rates of over 80% for all the analyte...

  10. An ultrasound-assisted digestion method for the determination of toxic element concentrations in ash samples by inductively coupled plasma optical emission spectrometry

    OpenAIRE

    Ilander, Aki; Väisänen, Ari

    2007-01-01

    method of ultrasound-assisted digestion followed by inductively coupled plasma optical emission spectrometry (ICP-OES) used for the determination of toxic element concentrations (arsenic, barium, cobalt, copper, lead, nickel, strontium, vanadium and zinc) in ash samples was developed. All the measurements were performed in robust plasma conditions which were tested by measuring the Mg(II) 280.270 nm/Mg(I) 285.213 nm line intensity ratios. The highest line intensity ratios were observed when a...

  11. Partial microwave-assisted wet digestion of animal tissue using a baby-bottle sterilizer for analyte determination by inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Matos, Wladiana O. [Grupo de Analise Instrumental Aplicada, Universidade Federal de Sao Carlos, Sao Carlos SP (Brazil); Grupo de Analise Instrumental Aplicada, Embrapa Pecuaria Sudeste, Sao Carlos, SP (Brazil)], E-mail: wladianamatos@yahoo.com.br; Menezes, Eveline A. [Grupo de Analise Instrumental Aplicada, Universidade Federal de Sao Carlos, Sao Carlos SP (Brazil); Grupo de Analise Instrumental Aplicada, Embrapa Pecuaria Sudeste, Sao Carlos, SP (Brazil); Gonzalez, Mario H. [Grupo de Analise Instrumental Aplicada, Universidade Federal de Sao Carlos, Sao Carlos SP (Brazil); Costa, Leticia M. [Departamento de Quimica-ICEx, Universidade Federal de Minas Gerais, Belo Horizonte MG (Brazil); Trevizan, Lilian C. [Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Piracicaba SP (Brazil); Nogueira, Ana Rita A. [Grupo de Analise Instrumental Aplicada, Embrapa Pecuaria Sudeste, Sao Carlos, SP (Brazil)

    2009-06-15

    A procedure for partial digestion of bovine tissue is proposed using polytetrafluoroethylene (PTFE) micro-vessels inside a baby-bottle sterilizer under microwave radiation for multi-element determination by inductively coupled plasma optical emission spectrometry (ICP OES). Samples were directly weighed in laboratory-made polytetrafluoroethylene vessels. Nitric acid and hydrogen peroxide were added to the uncovered vessels, which were positioned inside the baby-bottle sterilizer, containing 500 mL of water. The hydrogen peroxide volume was fixed at 100 {mu}L. The system was placed in a domestic microwave oven and partial digestion was carried out for the determination of Ca, Cu, Fe, Mg, Mn and Zn by inductively coupled plasma optical emission spectrometry. The single-vessel approach was used in the entire procedure, to minimize contamination in trace analysis. Better recoveries and lower residual carbon content (RCC) levels were obtained under the conditions established through a 2{sup 4-1} fractional factorial design: 650 W microwave power, 7 min digestion time, 50 {mu}L nitric acid and 50 mg sample mass. The digestion efficiency was ascertained according to the residual carbon content determined by inductively coupled plasma optical emission spectrometry. The accuracy of the proposed procedure was checked against two certified reference materials.

  12. Direct multielement trace analyses of silicon carbide powders by spark ablation simultaneous inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Kiera, Arne F.; Schmidt-Lehr, Sebastian; Song, Ming [Institute for Inorganic and Applied Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, D-20146 Hamburg (Germany); Bings, Nicolas H. [Institute for Inorganic and Applied Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, D-20146 Hamburg (Germany)], E-mail: bings@chemie.uni-hamburg.de; Broekaert, Jose A.C. [Institute for Inorganic and Applied Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, D-20146 Hamburg (Germany)

    2008-02-15

    A procedure for the direct analysis of silicon carbide powders (SiC) by simultaneous detection inductively coupled plasma optical emission spectrometry using a Spectro-CIROS{sup TM} spectrometer (CCD-ICP-OES) and a novel spark ablation system Spectro-SASSy (SA) as sample introduction technique is described. The sample preparation procedure for SA of non-conducting material is based on mixing the sample powders with a conducting matrix, in this case copper and briquetting pellets. Pressing time, pressure and mixing ratio are shown to be important parameters of the pelleting technique with respect to their mechanical stability for the reliability of the analysis results. A mixing ratio of 0.2 g +0.6 g for SiC and Cu, a pressure of 10 t cm{sup -2} and a pressing time of 8 min have been found optimum. It has also been shown that the spark parameters selected are crucial for uniform volatilization. Electron probe micrographs of the burning spots and the analytical signal magnitude showed that a rather hard spark at 100 Hz was optimum. The determination of trace elements in silicon carbide powders is demonstrated using a calibration based on the addition of standard solutions. For Al, Ti, V, Mn and Fe detection limits in the lower {mu}g g{sup -1} range can be achieved. Internal standardization with Y in combination with the addition of standard solutions allows relative standard deviations in the range of 4 to 24% for concentration levels of the order of 3 to 350 {mu}g g{sup -1}.

  13. Macro- and micro-element analysis in milk samples by inductively coupled plasma-optical emission spectrometry

    Directory of Open Access Journals (Sweden)

    Petrović Sanja M.

    2016-01-01

    Full Text Available The paper describes the determination of Ag, Al, B, Ba, Bi, Ca, Cd, Co, Cr, Cu, Fe, Ga, In, K, Li, Mg, Mn, Na, Ni, Pb, Sr, Tl and Zn, as well as total fat content of milk samples, originated from different sources. The analyzed milk samples were: human milk, fresh cow milk, pasteurized cow milk from a local market, and reconstituted powder milk. The milk samples were obtained from Jablanica District (Serbia territory. Preparation of samples for macro- and micro-analyses was done by wet digestion. Concentrations of the elements after digestion were determined by inductively coupled plasma optical emission spectrometry (ICP-OES. Total fat content of milk samples was determinate by the Weibull and Stoldt method. The results showed that potassium and calcium concentrations were the highest in all samples: 1840.64 - 2993.26 mg/L and 456.05 - 1318.08 mg/L, respectively. Of all heavy metals from the examined milk samples (copper, zinc, manganese, nickel, cadmium, and lead, the most common were zinc and copper, with approximately similar content in the range of 5 - 12 mg/l, while cadmium nickel and manganese were not detected at all. Samples of fresh cow milk and human milk showed the highest fat content of 3.6 and 4.2 %, respectively. Results for total fat and macro- and micro-analyses showed that fresh cow milk has the highest contents of fat and calcium, making it the most nutritious. [Projekat Ministarstva nauke Republike Srbije, br. TR 34012

  14. Low gas flow inductively coupled plasma optical emission spectrometry for the analysis of food samples after microwave digestion.

    Science.gov (United States)

    Nowak, Sascha; Gesell, Monika; Holtkamp, Michael; Scheffer, Andy; Sperling, Michael; Karst, Uwe; Buscher, Wolfgang

    2014-11-01

    In this work, the recently introduced low flow inductively coupled plasma optical emission spectrometry (ICP-OES) with a total argon consumption below 0.7 L/min is applied for the first time to the field of food analysis. One goal is the investigation of the performance of this low flow plasma compared to a conventional ICP-OES system when non-aqueous samples with a certain matrix are introduced into the system. For this purpose, arsenic is determined in three different kinds of fish samples. In addition several nutrients (K, Na, Mg, Ca) and trace metals (Co, Cu, Mn, Cd, Pb, Zn, Fe, and Ni) are determined in honey samples (acacia) after microwave digestion. The precision of the measurements is characterized by relative standard deviations (RSD) and compared to the corresponding precision values achieved using the conventional Fassel-type torch of the ICP. To prove the accuracy of the low flow ICP-OES method, the obtained data from honey samples are validated by a conventional ICP-OES. For the measurements concerning arsenic in fish, the low flow ICP-OES values are validated by conventional Fassel-type ICP-OES. Furthermore, a certified reference material was investigated with the low gas flow setup. Limits of detection (LOD), according to the 3σ criterion, were determined to be in the low microgram per liter range for all analytes. Recovery rates in the range of 96-106% were observed for the determined trace metal elements. It was proven that the low gas flow ICP-OES leads to results that are comparable with those obtained with the Fassel-type torch for the analysis of food samples.

  15. Slurry micro-sampling technique for use in argon-helium microwave induced plasma optical emission spectrometry.

    Science.gov (United States)

    Ślachciński, Mariusz

    2016-12-01

    The Flow Focusing Pneumatic Nebulizer (FFPN) working at low liquid flow rates was evaluated for the elemental analysis in slurried samples by argon-helium microwave induced plasma optical emission spectrometry (MIP-OES). The obtained results achieved were compared with commercially available V-groove Babington type nebulizer (VBPN). A univariate approach and the simplex optimization procedure were used to achieve optimized conditions and derive analytical figures of merit. Analytical performance of the micro nebulization system was characterized by a determination of the limits of detection (LODs), the precision (RSDs) and the wash-out times for Ba, Ca, Cd, Cu, Fe, Mg, Mn, Pb and Sr. The experimental concentration detection limits for simultaneous determination, calculated as the concentration giving a signal equal to three times of the standard deviation of the blank (LOD, 3σblank criterion, peak height) were 0.9, 0.2, 0.3, 0.2, 0.3, 0.1, 0.2, 0.4, 0.4 and 0.3ngmL(-1) for Ba, Ca, Cd, Cu, Fe, Mg, Mn, Pb and Sr, respectively. The method offers relatively good precision (RSD ranged from 5% to 8%) for micro-slurry sampling analysis. Analyses of the certified reference materials (NRCC DOLT-2, GBW 07302 and SRM 2710) were performed in order to determine the accuracy available with the presented nebulization systems. The measured contents of elements in the reference materials were in satisfactory agreement with the certified values. In addition, these elements were determined in two real samples. Slurry concentration up to 3% m/v (particles technique. An ultrasonic probe was used to homogenize the slurry in the polypropylene bottle just before its introduction into the nebulizer. The nebulizers exhibited no clogging problems. Copyright © 2016 Elsevier B.V. All rights reserved.

  16. Determination of metals in coal fly ashes using ultrasound-assisted digestion followed by inductively coupled plasma optical emission spectrometry.

    Science.gov (United States)

    Pontes, Fernanda V M; Mendes, Bruna A de O; de Souza, Evelyn M F; Ferreira, Fernanda N; da Silva, Lílian I D; Carneiro, Manuel C; Monteiro, Maria I C; de Almeida, Marcelo D; Neto, Arnaldo A; Vaitsman, Delmo S

    2010-02-05

    A method for determination of Co, Cr, Cu, Fe, Mn, Ni, Ti, V and Zn in coal fly ash samples using ultrasound-assisted digestion followed by inductively coupled plasma optical emission spectrometry (ICP-OES) is proposed. The digestion procedure consisted in the sonication of the previously dried sample with hydrofluoric acid and aqua regia at 80 degrees C for 30 min, elimination of fluorides by heating until dryness for about 1h and dissolution of the residue with nitric acid solution. A classical digestion method, used as comparative method, consisted in the addition of HCl, HNO(3) and HF to 1 g of sample, and heating on a hot plate until dryness for about 6h. The proposed method presents several advantages: it requires lower amounts of sample and reagents, and it is faster. It is also advantageous when compared to the published methods, which also use ultrasound-assisted digestion procedure: lower detection limits for Co, Cu, Ni, V and Zn, and it does not require shaking during the digestion. The detection limits (microg g(-1)) for Co, Cr, Cu, Fe, Mn, Ni, Ti, V and Zn were 0.06, 0.37, 1.0, 25, 0.93, 0.45, 4.0, 1.7 and 4.3, respectively. The results were in good agreement with those obtained by the classical method and reference values. The exception was Cr, which presented low recoveries in classical and proposed methods (83 and 87%, respectively). Also, the concentration for Cu obtained by the proposed method was significantly different from the reference value, in spite of the good recovery (91+/-1%).

  17. Selective Iron(III ion uptake using CuO-TiO2 nanostructure by inductively coupled plasma-optical emission spectrometry

    Directory of Open Access Journals (Sweden)

    Rahman Mohammed M

    2012-12-01

    Full Text Available Abstract Background CuO-TiO2 nanosheets (NSs, a kind of nanomaterials is one of the most attracting class of transition doped semiconductor materials due to its interesting and important optical, electrical, and structural properties and has many technical applications, such as in metal ions detection, photocatalysis, Chemi-sensors, bio-sensors, solar cells and so on. In this paper the synthesis of CuO-TiO2 nanosheets by the wet-chemically technique is reported. Methods CuO-TiO2 NSs were prepared by a wet-chemical process using reducing agents in alkaline medium and characterized by UV/vis., FT-IR spectroscopy, X-ray photoelectron spectroscopy (XPS, powder X-ray diffraction (XRD, and field-emission scanning electron microscopy (FE-SEM etc. Results The structural and optical evaluation of synthesized NSs were measured by XRD pattern, Fourier transform infrared (FT-IR and UV–vis spectroscopy, respectively which confirmed that the obtained NSs are well-crystalline CuO-TiO2 and possessing good optical properties. The morphological analysis of CuO-TiO2 NSs was executed by FE-SEM, which confirmed that the doped products were sheet-shaped and growth in large quantity. Here, the analytical efficiency of the NSs was applied for a selective adsorption of iron(III ion prior to detection by inductively coupled plasma-optical emission spectrometry (ICP-OES. The selectivity of NSs towards various metal ions, including Au(III, Cd(II, Co(II, Cr(III, Fe(III, Pd(II, and Zn(II was analyzed. Conclusions Based on the selectivity study, it was confirmed that the selectivity of doped NSs phase was the most towards Fe(III ion. The static adsorption capacity for Fe(III was calculated to be 110.06 mgg−1. Results from adsorption isotherm also verified that the adsorption process was mainly monolayer-adsorption onto a surface containing a finite number of CuO-TiO2 NSs adsorption sites.

  18. Sequential cloud point extraction for the speciation of mercury in seafood by inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Li Yingjie [Department of Chemistry, Wuhan University, Wuhan 430072 (China); Hu Bin [Department of Chemistry, Wuhan University, Wuhan 430072 (China)], E-mail: binhu@whu.edu.cn

    2007-10-15

    A novel nonchromatographic speciation technique for the speciation of mercury by sequential cloud point extraction (CPE) combined with inductively coupled plasma optical emission spectrometry (ICP-OES) was developed. The method based on Hg{sup 2+} was complexed with I{sup -} to form HgI{sub 4}{sup 2-}, and the HgI{sub 4}{sup 2-} reacted with the methyl green (MG) cation to form hydrophobic ion-associated complex, and the ion-associated complex was then extracted into the surfactant-rich phase of the non-ionic surfactant octylphenoxypolyethoxyethanol (Triton X-114), which are subsequently separated from methylmercury (MeHg{sup +}) in the initial solution by centrifugation. The surfactant-rich phase containing Hg(II) was diluted with 0.5 mol L{sup -1} HNO{sub 3} for ICP-OES determination. The supernatant is also subjected to the similar CPE procedure for the preconcentration of MeHg{sup +} by the addition of a chelating agent, ammonium pyrrolidine dithiocarbamate (APDC), in order to form water-insolvable complex with MeHg{sup +}. The MeHg{sup +} in the micelles was directly analyzed after disposal as describe above. Under the optimized conditions, the extraction efficiency was 93.5% for Hg(II) and 51.5% for MeHg{sup +} with the enrichment factor of 18.7 for Hg(II) and 10.3 for MeHg{sup +}, respectively. The limits of detection (LODs) were 56.3 ng L{sup -1} for Hg(II) and 94.6 ng L{sup -1} for MeHg{sup +} (as Hg) with the relative standard deviations (RSDs) of 3.6% for Hg(II) and 4.5% for MeHg{sup +} (C = 10 {mu}g L{sup -1}, n = 7), respectively. The developed technique was applied to the speciation of mercury in real seafood samples and the recoveries for spiked samples were found to be in the range of 93.2-108.7%. For validation, a certified reference material of DORM-2 (dogfish muscle) was analyzed and the determined values are in good agreement with the certified values.

  19. Sequential cloud point extraction for the speciation of mercury in seafood by inductively coupled plasma optical emission spectrometry

    Science.gov (United States)

    Li, Yingjie; Hu, Bin

    2007-10-01

    A novel nonchromatographic speciation technique for the speciation of mercury by sequential cloud point extraction (CPE) combined with inductively coupled plasma optical emission spectrometry (ICP-OES) was developed. The method based on Hg 2+ was complexed with I - to form HgI 42-, and the HgI 42- reacted with the methyl green (MG) cation to form hydrophobic ion-associated complex, and the ion-associated complex was then extracted into the surfactant-rich phase of the non-ionic surfactant octylphenoxypolyethoxyethanol (Triton X-114), which are subsequently separated from methylmercury (MeHg +) in the initial solution by centrifugation. The surfactant-rich phase containing Hg(II) was diluted with 0.5 mol L - 1 HNO 3 for ICP-OES determination. The supernatant is also subjected to the similar CPE procedure for the preconcentration of MeHg + by the addition of a chelating agent, ammonium pyrrolidine dithiocarbamate (APDC), in order to form water-insolvable complex with MeHg +. The MeHg + in the micelles was directly analyzed after disposal as describe above. Under the optimized conditions, the extraction efficiency was 93.5% for Hg(II) and 51.5% for MeHg + with the enrichment factor of 18.7 for Hg(II) and 10.3 for MeHg +, respectively. The limits of detection (LODs) were 56.3 ng L - 1 for Hg(II) and 94.6 ng L - 1 for MeHg + (as Hg) with the relative standard deviations (RSDs) of 3.6% for Hg(II) and 4.5% for MeHg + ( C = 10 μg L -1, n = 7), respectively. The developed technique was applied to the speciation of mercury in real seafood samples and the recoveries for spiked samples were found to be in the range of 93.2-108.7%. For validation, a certified reference material of DORM-2 (dogfish muscle) was analyzed and the determined values are in good agreement with the certified values.

  20. Chemical Characterisation of Bulk and Melt-spun Ribbons of NiMnIn Alloy using Inductively Coupled Plasma Optical Emission Spectrometry

    Directory of Open Access Journals (Sweden)

    S.S. Kalyan Kamal

    2011-05-01

    Full Text Available Method development for the analysis of NiMnIn, a new magnetocaloric effect (MCE material using inductively-coupled plasma optical emission spectrometry (ICPOES is discussed. Spectral interference of Ni and Mn on the analysis of In were studied. The process of method validation was carried out using various analytical techniques like conventional wet chemical techniques and instrumental techniques such as atomic absorption spectrometry. All the techniques show a close agreement in values, thus this method could be applied for regular analysis of NiMnIn alloys. A comparative chemical analysis of bulk and melt-spun ribbons of this alloy is also discussed.

  1. Chemical Characterisation of Bulk and Melt-spun Ribbons of NiMnIn alloy using Inductively Coupled Plasma Optical Emission Spectrometry

    Directory of Open Access Journals (Sweden)

    S.S. Kalyan Kamal

    2011-04-01

    Full Text Available Method development for the analysis of NiMnIn, a new magnetocaloric effect (MCE material using inductively coupled plasma optical emission spectrometry (ICPOES is discussed. Spectral interference of Ni and Mn on the analysis of In were studied. The process of method validation was carried out using various analytical techniques like conventional wet chemical techniques and instrumental techniques such as atomic absorption spectrometry. All the techniques show a close agreement in values, thus this method could be applied for regular analysis of NiMnIn alloys. A comparative chemical analysis of bulk and melt-spun ribbons of this alloy is also discussed.Defence Science Journal, 2011, 61(3, pp.270-274, DOI:http://dx.doi.org/10.14429/dsj.61.397

  2. [Determination of nine hazardous elements in textiles by inductively coupled plasma optical emission spectrometer after microwave-assisted dilute nitric acid extraction].

    Science.gov (United States)

    Chen, Fei; Xu, Dian-dou; Tang, Xiao-ping; Cao, Jing; Liu, Ya-ting; Deng, Jian

    2012-01-01

    Textiles are easily contaminated by heavy metals in the course of processing. In order to monitor the quality of textiles, a new method was developed for simultaneous determination of arsenic, antimony, lead, cadmium, chromium, cobalt, copper, nickel and mercury in textiles by inductively coupled plasma optical emission spectrometry (ICP-OES) after microwave-assisted dilute nitric acid extraction. After optimizing extraction conditions, we ultimately selected 5% nitric acid as extractant and 5 min as extraction time with the extraction temperature of 120 degrees C and instrument power of 400W in the microwave-assisted extraction procedure. Nine hazardous elements were detected sequentially by ICP-OES. The results showed that the detection limits were 0.3-15 microg x L(-1) and the recoveries 73.6%-105% with the RSDs (n = 3) of 0.1%-3%. The proposed method was successfully used to determine nine elements in cotton, wool, terylene and acrylic.

  3. Metal and metalloid determination in bioethanol through inductively coupled plasma-optical emission spectroscopy

    Science.gov (United States)

    Sánchez, Carlos; Lienemann, Charles-Philippe; Todolí, José-Luis

    2016-01-01

    A new method to carry out the elemental determination of metals in bioethanol through ICP-OES has been developed. The procedure is based on the use of a heated torch integrated sample introduction system (hTISIS) to directly introduce the vaporized sample into the plasma. Two injection modes (continuous liquid aspiration and air-segmented flow injection analysis) have been evaluated. In a first step, the matrix effects caused by several ethanol-water mixtures were removed by operating the hTISIS at 400 °C in segmented injection. Meanwhile, the results also proved that the system could be operated in continuous mode at 200 °C with the complete interference removal. Finally, twenty-eight real samples with bioethanol contents between 55% and 100% were analyzed with the methods previously developed. Regarding validation, recoveries from 80% to 120% were obtained for 18 analytes and the concentrations found with the proposed method were in agreement with those encountered with a preconcentration method, taken as a reference procedure. Limits of detection went from 3 ng mL- 1 for manganese to about 500 ng mL- 1 for calcium. This allowed to quantify Cr, Fe, Mg, Mn and Zn in segmented flow injection and Al, Cd, Cr, Cu, K, Mg, Mn, Na and Zn in continuous sample aspiration mode in bioethanol samples.

  4. Optimization of the operating conditions of solid sampling electrothermal vaporization coupled to inductively coupled plasma optical emission spectrometry for the sensitive direct analysis of powdered rice.

    Science.gov (United States)

    Sadiq, Nausheen; Beauchemin, Diane

    2014-12-03

    Two different approaches were used to improve the capabilities of solid sampling (SS) electrothermal vaporization (ETV) coupled to inductively coupled plasma optical emission spectrometry (ICP-OES) for the direct analysis of powdered rice. Firstly, a cooling step immediately before and after the vaporization step in the ETV temperature program resulted in a much sharper analyte signal peak. Secondly, point-by-point internal standardization with an Ar emission line significantly improved the linearity of calibration curves obtained with an increasing amount of rice flour certified reference material (CRM). Under the optimized conditions, detection limits ranged from 0.01 to 6ngg(-1) in the solid, depending on the element and wavelength selected. The method was validated through the quantitative analysis of corn bran and wheat flour CRMs. Application of the method to the multi-elemental analysis of 4-mg aliquots of real organic long grain rice (white and brown) also gave results for Al, As, Co, Cu, Fe, Mg, Se, Pb and Zn in agreement with those obtained by inductively coupled plasma mass spectrometry following acid digestion of 0.2-g aliquots. As the analysis takes roughly 5min per sample (2.5min for grinding, 0.5-1min for weighing a 4-mg aliquot and 87s for the ETV program), this approach shows great promise for fast screening of food samples.

  5. Straightforward way to enhance robustness in ultrasonic nebulization-axial view inductively coupled plasma optical emission spectrometry via an additional N2 gas stream

    Science.gov (United States)

    Scheffler, Guilherme Luiz; Pozebon, Dirce

    2015-11-01

    In the present study a low flow of N2 is mixed with the aerosol produced by ultrasonic nebulization (USN) prior analysis using inductively coupled plasma optical emission spectrometry (ICP OES). The foreign gas is added for improving plasma characteristics in axially-viewed ICP. By computing the Mg ionic to atomic ratio (plasma robustness) it was concluded that N2 dissociates closer to the load coil when USN is used as sample introduction system. The maximum emission intensity of Mg(II) for pneumatic nebulization (PN) was observed at 11 mm from the load coil while it was 8 mm for USN, indicating earlier aerosol desolvation, atomization and excitation processes in the ICP. Emission profiles of Ar(I) 415.861 nm, Ba(II) 486.601 nm and Ba(II) 233.527 nm indicated that metastable Ar species are overpopulated in the ICP under the N2 flow. Copper and manganese ionic lines with energy close to 16 eV (Ar ionization) were monitored to evaluate spatially dependent charge-transfer reaction along the ICP axis in the presence and absence of the N2 flow. The Cu(II) signal profiles indicated abundance of Ar+ species at low distances from the load coil when N2 was added. On the other hand, differences were not observed at longer distances from the load coil for both plasmas (mixed-gas and pure Ar-ICP). The calculated limits of detection (LODs) for both plasmas had the same order of magnitude. Analysis of certified reference samples demonstrated that the accuracy was preserved by adding the low flow of N2. It was concluded that adding a low flow of N2 to the aerosol produced by USN is a simple way to increase plasma robustness, which is usually lower than that achieved using conventional PN.

  6. Use of factorial design for evaluation of plasma conditions and comparison of two liquid sample introduction systems for an axially viewed inductively coupled plasma optical emission spectrometer

    Energy Technology Data Exchange (ETDEWEB)

    Trevizan, Lilian C. [Grupo de Analise Instrumental Aplicada, Departamento de Quimica, Universidade Federal de Sao Carlos, Caixa Postal 676, Sao Carlos, SP, 13650-970 (Brazil); Vieira, Edivan C. [Grupo de Analise Instrumental Aplicada, Departamento de Quimica, Universidade Federal de Sao Carlos, Caixa Postal 676, Sao Carlos, SP, 13650-970 (Brazil); Embrapa Pecuaria Sudeste, Sao Carlos, SP (Brazil); Nogueira, Ana Rita A. [Embrapa Pecuaria Sudeste, Sao Carlos, SP (Brazil); Nobrega, Joaquim A. [Grupo de Analise Instrumental Aplicada, Departamento de Quimica, Universidade Federal de Sao Carlos, Caixa Postal 676, Sao Carlos, SP, 13650-970 (Brazil)]. E-mail: djan@terra.com.br

    2005-06-30

    A factorial design was applied to evaluate plasma conditions employing the Mg II 280/Mg I 285 nm intensity ratio in an axially viewed inductively coupled plasma optical emission spectrometer using different sample introduction devices: a concentric or a V-groove nebulizer and a cyclonic or a Sturman-Masters spray chamber. Effects of nebulizer gas flow-rate on Mg II/Mg I ratio were different in each introduction system. Robust conditions were obtained at low nebulizer gas flow-rate when using concentric nebulizer with a cyclonic spray chamber or a concentric nebulizer and a Sturman-Masters spray chamber. However, when using a V-groove nebulizer with a Sturman-Masters spray chamber, Mg II/Mg I ratio increased at high nebulizer gas flow-rates. Recovery experiments for a milk standard reference material diluted in water-soluble tertiary amines in both robust and non-robust conditions indicated that the robust condition was reached at higher nebulizer gas flow-rates and led to better accuracy and precision when using a V-groove nebulizer.

  7. Investigation of the direct hydride generation nebulizer for the determination of arsenic, antimony and selenium in inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Rojas, Illiana; Murillo, Miguel; Carrion, Nereida; Chirinos, Jose [Centro de Quimica Analitica, Escuela de Quimica, Facultad de Ciencias, Universidad Central de Venezuela, P.O. Box 47102, 1041a, Caracas (Venezuela)

    2003-05-01

    A direct hydride generation nebulizer (DHGN) was explored for introduction of the sample in inductively coupled plasma-optical emission spectrometry (ICP-OES) using radially viewed mode. This simple hydride generation system was constructed in our laboratory and requires similar plasma operating conditions to conventional nebulizer-spray-chamber arrangements. This work was focused on the optimization of the operating conditions for hydride generation and evaluation of the main analytical figures of merit for the determination of As, Sb and Se. The excitation conditions of the ICP-OES instrument operated with the DHGN were also explored. Results showed that the analytical performance of the new system for the determination of As, Sb and Se was superior to that of conventional nebulization systems. The DHGN also enabled the determination of elements that do not form volatile hydrides, but with less sensitivity than conventional nebulization systems. Evaluation of the plasma robustness showed that gases generated in hydride generation do not significantly affects the plasma discharge. Similar to conventional hydride generation techniques, analysis with DHGN was susceptible to non-spectroscopic interferences produced by transition metals. Finally, the utility of the DHGN in practical ICP-OES studies was demonstrated in the determination of trace elements in an oyster tissue standard reference material. (orig.)

  8. Introduction of organic/hydro-organic matrices in inductively coupled plasma optical emission spectrometry and mass spectrometry: a tutorial review. Part II. Practical considerations.

    Science.gov (United States)

    Leclercq, Amélie; Nonell, Anthony; Todolí Torró, José Luis; Bresson, Carole; Vio, Laurent; Vercouter, Thomas; Chartier, Frédéric

    2015-07-23

    Inductively coupled plasma optical emission spectrometry (ICP-OES) and mass spectrometry (ICP-MS) are increasingly used to carry out analyses in organic/hydro-organic matrices. The introduction of such matrices into ICP sources is particularly challenging and can be the cause of numerous drawbacks. This tutorial review, divided in two parts, explores the rich literature related to the introduction of organic/hydro-organic matrices in ICP sources. Part I provided theoretical considerations associated with the physico-chemical properties of such matrices, in an attempt to understand the induced phenomena. Part II of this tutorial review is dedicated to more practical considerations on instrumentation, instrumental and operating parameters, as well as analytical strategies for elemental quantification in such matrices. Two important issues are addressed in this part: the first concerns the instrumentation and optimization of instrumental and operating parameters, pointing out (i) the description, benefits and drawbacks of different kinds of nebulization and desolvation devices and the impact of more specific instrumental parameters such as the injector characteristics and the material used for the cone; and, (ii) the optimization of operating parameters, for both ICP-OES and ICP-MS. Even if it is at the margin of this tutorial review, Electrothermal Vaporization and Laser Ablation will also be shortly described. The second issue is devoted to the analytical strategies for elemental quantification in such matrices, with particular insight into the isotope dilution technique, particularly used in speciation analysis by ICP-coupled separation techniques.

  9. Determination of Se in biological samples by axial view inductively coupled plasma optical emission spectrometry after digestion with aqua regia and on-line chemical vapor generation

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Eder Jose dos [Instituto de Tecnologia do Parana (TECPAR), 81350-010 Curitiba, PR (Brazil)], E-mail: eder@tecpar.br; Herrmann, Amanda Beatriz; Kulik de Caires, Suzete [Instituto de Tecnologia do Parana (TECPAR), 81350-010 Curitiba, PR (Brazil); Azzolin Frescura, Vera Lucia; Curtius, Adilson Jose [Departamento de Quimica, Universidade Federal de Santa Catarina (UFSC), 880400-900 Florianopolis, SC (Brazil)

    2009-06-15

    A simple and fast method for the determination of Se in biological samples, including food, by axial view inductively coupled plasma optical emission spectrometry using on-line chemical vapor generation (CVG-ICP OES) is proposed. The concentrations of HCl and NaBH{sub 4}, used in the chemical vapor generation were optimized by factorial analysis. Six certified materials (non-fat milk powder, lobster hepatopancreas, human hair, whole egg powder, oyster tissue, and lyophilised pig kidney) were treated with 10 mL of aqua regia in a microwave system under reflux for 15 min followed by additional 15 min in an ultrasonic bath. The solutions were transferred to a 100 mL volumetric flask and the final volume was made up with water. The Se was determined directly in these solutions by CVG-ICP OES, using the analytical line at 196.026 nm. Calibration against aqueous standards in 10% v/v aqua regia in the concentration range of 0.5-10.0 {mu}g L{sup -} {sup 1} Se(IV) was used for the analysis. The quantification limit, considering a 0.5 g sample weight in a final volume of 100 mL{sup -} {sup 1} was 0.10 {mu}g g{sup -} {sup 1}. The obtained concentration values were in agreement with the total certified concentrations, according to the t-test for a 95% confidence level.

  10. Speciation of inorganic selenium in environmental water samples by inductively coupled plasma optical emission spectrometry after preconcentration by using a mesoporous zirconia coating on coal cinder.

    Science.gov (United States)

    Wei, Xiao-Shu; Wu, Yi-Wei; Han, Li-Juan; Guo, Jing; Sun, Hong-Li

    2014-08-01

    A simple, novel, and selective flow-injection solid-phase extraction with inductively coupled plasma optical emission spectrometry method was developed for the speciation of inorganic selenium in environmental water samples. A mesoporous zirconia film was simply introduced to coat coal cinder by means of the sol-gel technique, and the adsorptive performance of the coated material for Se(IV)/Se(VI) was investigated in different media. Both Se(IV) and Se(VI) can be retained quantitatively by the material in HCl/NaOH (pH 1.0-9.0) media, while only Se(IV) was adsorbed quantitatively in sodium acetate buffer (pH 3.5-6.0). Thus, the assay of Se(VI) is based on subtracting Se(IV) from total selenium by controlling different adsorptive media without employing any redox procedure. Under the optimum conditions, the detection limit of Se(IV) is 9.0 ng/L with an enrichment factor of 100, and the relative standard deviation is 3.6% (n = 9, C = 5.0 ng/mL). The developed method was successfully applied to the speciation of inorganic selenium in environmental water samples with satisfactory results. In order to further verify the accuracy of the developed method, it was applied to analysis of total selenium in GSBZ 50031-94 certified reference environmental water, and the determined values coincided with the certified values very well.

  11. Optimization of an open-focused microwave oven digestion procedure for determination of metals in diesel oil by inductively coupled plasma optical emission spectrometry.

    Science.gov (United States)

    Sant'Ana, Flavio W; Santelli, Ricardo E; Cassella, Alessandra R; Cassella, Ricardo J

    2007-10-01

    This work reports the optimization of a focused microwave assisted procedure for the wet acid dissolution of diesel oil in order to allow the determination of metals in the samples by inductively coupled plasma optical emission spectrometry (ICP-OES). The dissolution process was monitored by measuring residual carbon content (RCC), also by ICP-OES, in the final solutions obtained after application of digestion program. All experimental work was performed using a commercial sample of diesel oil containing 85.74+/-0.13% of carbon. The initial dissolution program comprised three steps: (i) carbonization with H(2)SO(4); (ii) oxidation with HNO(3) and (iii) final oxidation with H(2)O(2). During work it was verified that the first step played an important role on the dissolution process of this kind of sample. It is therefore, necessary to give a detailed optimization of such step. Employing the optimized conditions it was possible to digest 2.5 g of diesel oil with a 40 min-heating program. At these conditions, residual carbon content was always lower than 5%. Optimized methodology was applied in the determination of metals in three diesel oil samples by ICP-OES. Recovery tests were also performed by adding 10 microg of metals, as organic standards, to the samples before digestion. Recovery percentages always higher than 90% were obtained for the metals of interest (Al, Cu, Fe and Ni), except for Zn, which presented recoveries between 70 and 78%.

  12. Determination of arsenic, cadmium, cobalt, chromium, lead, molybdenum, nickel, and selenium in fertilizers by microwave digestion and inductively coupled plasma-optical emission spectrometry detection: collaborative study.

    Science.gov (United States)

    Kane, Peter F; Hall, William L

    2006-01-01

    There is increasing regulatory interest in the non-nutritive metals content of fertilizer materials, but at present there is no consensus analytical method for acid digestion and instrument detection of those elements in fertilizer matrixes. This lack of method standardization has resulted in unacceptable variability of results between fertilizer laboratories performing metals analysis. A method has been developed using microwave digestion with nitric acid at 200 degrees C, followed by inductively coupled plasma-optical emission spectrometry instrument detection, for the elements arsenic, cadmium, cobalt, chromium, molybdenum, nickel, lead, and selenium. The method has been collaboratively studied, and statistical results are here reported. Fourteen collaborators were sent 62 sample materials in a blind duplicate design. Materials represented a broad cross section of fertilizer types, including phosphate ore, manufactured phosphate products, N-P-K blends, organic fertilizers, and micro-nutrient materials. As much as possible within the limit of the number of samples, materials were selected from different regions of the United States and the world. Limit of detection (LOD) was determined using synthetic fertilizers consisting of reagent grade chemicals with near zero levels of the non-nutritive elements, analyzed blindly. Samples with high iron content caused the most variability between laboratories. Most samples reasonably above LOD gave HorRat values within the range 0.5 to 2.0, indicating acceptable method performance according to AOAC guidelines for analyses in the mg/kg range. The method is recommended for AOAC Official First Action status.

  13. The determination of trace element concentrations in fly ash samples using ultrasound-assisted digestion followed with inductively coupled plasma optical emission spectrometry.

    Science.gov (United States)

    Ilander, Aki; Väisänen, Ari

    2009-08-01

    A method of ultrasound-assisted digestion followed by inductively coupled plasma optical emission spectrometry (ICP-OES) used for the determination of trace element (chromium, copper, lead, nickel, vanadium and zinc) concentrations in fly ash samples was developed. All the measurements were performed in robust plasma conditions. Ultrasound-assisted digestion procedures using digestion solutions of aqua regia and hydrofluoric acid (HF) resulted in recovery rates of over 80% for all the analyte elements. Ultrasound-assisted two-step digestion with digestion solutions of 6mL of HNO(3) (Step 1) and 3mL of HNO(3)+3mL of HF (Step 2) resulted in recovery rates of over 92% for all the analyte elements with one exception, chromium, which had a recovery of about 85%. The analysis of SRM 1633b showed that the two-step ultrasound-assisted digestion method developed resulted in chromium, copper, nickel and zinc concentrations higher than the microwave digestion method standardized by the United States Environmental Protection Agency (USEPA method 3052). This is the very first time when a digestion method using ultrasound resulted in higher efficiency than microwave (USEPA method 3052) for chromium and nickel in very hard to dissolve samples. The major advantages of the ultrasound-assisted digestion over microwave digestion is the high treatment rate (about 30 samples simultaneously with a sonication time of 18min) and the possibility to use new sample vessels without a significant increase in costs.

  14. An ultrasound-assisted digestion method for the determination of toxic element concentrations in ash samples by inductively coupled plasma optical emission spectrometry.

    Science.gov (United States)

    Ilander, Aki; Väisänen, Ari

    2007-10-29

    A method of ultrasound-assisted digestion followed by inductively coupled plasma optical emission spectrometry (ICP-OES) used for the determination of toxic element concentrations (arsenic, barium, cobalt, copper, lead, nickel, strontium, vanadium and zinc) in ash samples was developed. All the measurements were performed in robust plasma conditions which were tested by measuring the Mg(II) 280.270 nm/Mg(I) 285.213 nm line intensity ratios. The highest line intensity ratios were observed when a nebulizer gas flow of 0.6 L min(-1), auxiliary gas flow of 0.2 L min(-1) and plasma power of 1400 W were used for radially viewed plasma. The analysis of SRM 1633b showed that the ultrasound-assisted method developed is highly comparable with the microwave digestion method standardized by the United States Environmental Protection Agency (EPA-3052). The ultrasound-assisted digestion with a digestion solution of aqua regia and hydrofluoric acid (HF) resulted in recovery rates of over 81%. One exception is arsenic which resulted in recoveries of about 60% only; however, it could be digested with good recovery (>90%) using a digestion solution of 5 mL of water and 5 mL of aqua regia. The major advantage of the ultrasound-assisted digestion over microwave digestion is the high treatment rate (30 samples simultaneously with a sonication time of 18 min).

  15. Imaging of elements in leaves of tobacco by solid sampling–electrothermal vaporization–inductively coupled plasma-optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Masson, Pierre, E-mail: masson@bordeaux.inra.fr

    2014-12-01

    Plants take up and store elements according to the environment in which they are growing. Because plants are at the base of the food chain, the determination of essential elements or toxic elements in plant materials is of importance. However, it is assumed that the element content determined on selected tissues may provide more specific information than that derived from the whole plant analysis. In this work, we assessed the feasibility of solid sampling–electrothermal vaporization–inductively coupled plasma-optical emission spectrometry analyses for quantitative imaging of Cd and Mg in plant leaves. Leaves of tobacco (Nicotiana tabacum) were selected to be used as samples. To produce a two dimensional image, sections cut from leaf samples were analyzed. Cellulose doped with multi-element solution standards was used as calibration samples. Two certified reference materials (NIST SRM 1547 Peach Leaves and NIST SRM 1573a Tomato leaves) were used to verify the accuracy of measurements with good agreement between the measured concentrations and the certified values. Quantitative imaging revealed the inhomogeneous distribution of the selected elements. Excess of Cd and Mg tended to be focused on peripheral regions and the tip of the leaf.

  16. Determination of heavy metals and their speciation in street dusts by inductively coupled plasma-optical emission spectrometry after a Community Bureau of Reference sequential extraction procedure.

    Science.gov (United States)

    Altundag, Huseyin; Imamoglu, Mustafa; Doganci, Secil; Baysal, Erkan; Albayrak, Sinem; Tuzen, Mustafa

    2013-01-01

    Sequential selective extraction techniques are commonly used to fractionate the solid-phase forms of metals in soils. This procedure provides measurements of extractable metals from media, such as acetic acid (0.11 M), hydroxyl ammonium chloride (0.1 M), hydrogen peroxide (8.8 M) plus ammonium acetate (1 M), and aqua regia stages of the sequential extraction procedure. In this work, the extractable Pb, Cu, Mn, Sr, Ni, V, Fe, Zn, and Cr were evaluated in street dust samples from Sakarya, Turkey, between May and October 2009 using the three-step sequential extraction procedure described by the Community Bureau of Reference (BCR, now the Standards, Measurements, and Testing Programme) of the European Union. The sampling sites were divided into 10 categories; a total of 50 street dusts were analyzed. The determination of multielements in the samples was performed by inductively coupled plasma-optical emission spectrometry. Validation of the proposed method was performed using BCR 701 certified reference material. The results showed good agreement between the obtained and the certified values for the metals analyzed.

  17. Spectral interferences in the determination of rhenium in molybdenum and copper concentrates by inductively coupled plasma optical emission spectrometry (ICP-OES)

    Science.gov (United States)

    Karadjov, Metody; Velitchkova, Nikolaya; Veleva, Olga; Velichkov, Serafim; Markov, Pavel; Daskalova, Nonka

    2016-05-01

    This paper deals with spectral interferences of complex matrix containing Mo, Al, Ti, Fe, Mg, Ca and Cu in the determination of rhenium in molybdenum and copper concentrates by inductively coupled plasma optical emission spectrometry (ICP-OES). By radial viewing 40.68 MHz ICP equipped with a high resolution spectrometer (spectral bandwidth = 5 pm) the hyperfine structure (HFS) of the most prominent lines of rhenium (Re II 197.248 nm, Re II 221.426 nm and Re II 227.525 nm) was registered. The HFS components under high resolution conditions were used as separate prominent line in order to circumvent spectral interferences. The Q-concept was applied for quantification of spectral interferences. The quantitative databases for the type and the magnitude of the spectral interferences in the presence of above mentioned matrix constituents were obtained by using a radial viewing 40.68 MHz ICP with high resolution and an axial viewing 27.12 MHz ICP with middle resolution. The data for the both ICP-OES systems were collected chiefly with a view to spectrochemical analysis for comparing the magnitude of line and wing (background) spectral interference and the true detection limits with spectroscopic apparatus with different spectral resolution. The sample pretreatment methods by sintering with magnesium oxide and oxidizing agents as well as a microwave acid digestion were applied. The feasibility, accuracy and precision of the analytical results were experimentally demonstrated by certified reference materials.

  18. Simultaneous extraction and preconcentration of uranium and thorium in aqueous samples by new modified mesoporous silica prior to inductively coupled plasma optical emission spectrometry determination.

    Science.gov (United States)

    Yousefi, Seyed Reza; Ahmadi, Seyed Javad; Shemirani, Farzaneh; Jamali, Mohammad Reza; Salavati-Niasari, Masoud

    2009-11-15

    A new synthesized modified mesoporous silica (MCM-41) using 5-nitro-2-furaldehyde (fural) was applied as an effective sorbent for the solid phase extraction of uranium(VI) and thorium(IV) ions from aqueous solution for the measurement by inductively coupled plasma optical emission spectrometry (ICP OES). The influences of some analytical parameters on the quantitative recoveries of the analyte ions were investigated in batch method. Under optimal conditions, the analyte ions were sorbed by the sorbent at pH 5.5 and then eluted with 1.0 mL of 1.0 mol L(-1) HNO(3). The preconcentration factor was 100 for a 100mL sample volume. The limits of detection (LOD) obtained for uranium(VI) and thorium(IV) were 0.3 microg L(-1). The maximum sorption capacity of the modified MCM-41 was found to be 47 and 49 mg g(-1) for uranium(VI) and thorium(IV), respectively. The sorbent exhibited good stability, reusability, high adsorption capacity and fast rate of equilibrium for sorption/desorption of uranium and thorium ions. The applicability of the synthesized sorbent was examined using CRM and real water samples.

  19. Determination of rare earth elements in waters by inductively coupled plasma optical emission spectrometry after preconcentration with 6-(2-thienyl)-2-pyridinecarboxaldehyde functionalized Amberlite XAD-4 resin.

    Science.gov (United States)

    Karadaş, Cennet; Kara, Derya

    2014-01-01

    A new method has been developed for the determination of rare earth elements (REEs) (Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) in water samples based on preconcentration with a mini-column packed with 6-(2-thienyl)-2-pyridinecarboxaldehyde functionalized Amberlite XAD-4 resin prior to their determination using inductively coupled plasma optical emission spectrometry (ICP-OES). The optimum experimental parameters for preconcentration of REEs, such as pH of the sample, sample and eluent flow rates and sample volume, were investigated. The optimum pH values for quantitative (90-110%) sorption of the REE ions were between 6.0 and 8.0. The elution process was carried out using 2 mL of 1.0 mol L(-1) HNO3 solution. Under the optimum conditions, detection limits between 0.032 and 0.963 μg L(-1) for a 10 mL sample volume and 0.006 and 0.193 μg L(-1) for a 50 mL sample volume were determined. The proposed method was successfully applied to the determination of REEs in water samples with recoveries in the range of 90.1-110.5%.

  20. Tin Content Determination in Canned Fruits and Vegetables by Hydride Generation Inductively Coupled Plasma Optical Emission Spectrometry

    Directory of Open Access Journals (Sweden)

    Sanda Rončević

    2012-01-01

    Full Text Available Tin content in samples of canned fruits and vegetables was determined by hydride generation inductively coupled plasma atomic emission spectrometry (HG-ICP-OES, and it was compared with results obtained by standard method of flame atomic absorption spectrometry (AAS. Selected tin emission lines intensity was measured in prepared samples after addition of tartaric acid and followed by hydride generation with sodium borohydride solution. The most favorable line at 189.991 nm showed the best detection limit (1.9 μg L−1 and limit of quantification (6.4 μg kg−1. Good linearity and sensitivity were established from time resolved analysis and calibration tests. Analytical accuracy of 98–102% was obtained by recovery study of spiked samples. Method of standard addition was applied for tin determination in samples from fully protected tinplate. Tin presence at low-concentration range was successfully determined. It was shown that tenth times less concentrations of Sn were present in protected cans than in nonprotected or partially protected tinplate.

  1. Determination of total strontium in uruguayan rice by inductively coupled plasma optical emission spectrometry (ICP-OES

    Directory of Open Access Journals (Sweden)

    Mario E. Rivero Huguet

    2011-04-01

    Full Text Available Strontium (Sr is found naturally as a non-radioactive element and has 16 known isotopes. Naturally occurring Sr is found as four stable isotopes: Sr-84, -86, -87, and -88. Twelve other isotopes are radioactive. Sr-90 is the most important radioactive isotope in the environment, discovered mostly after the nuclear experiments conducted in the 1950s and 1960s. In the present work, 86 rice samples (Oryza saliva L. and 7 rice husk samples were digested by dry ashing for the purpose of determining the total Sr levels by ICP-OES. The mean concentrations found were: 0.281 µg g-1 for milled, 0.287 µg g-1 for parboiled milled, 0.564 µg g-1 for brown, 0.73 µg g-1 for parboiled brown, and 1.16 µg g-1 for paddy rice, and 3.44 µg g-1 for the rice husks. Validation of the method was conducted with a certified reference material, NIST CAM 8418 Wheat Gluten, and the recovery obtained ranged from 89-98%. As the outer layers (aleurone, pericarp of the grain are removed, the Sr concentration decreases. It can then be assumed that most of the Sr is stored in these layers. Although no extensive data exist for Sr levels in rice, the values obtained are in good agreement with the results reported for Sr in brown rice from Japan (0.25-0.72 µg g-1 and with non-contaminated foodstuffs from other parts of the world. Thus, the Uruguayan rice has Sr levels that match non-contaminated samples and its consumption presents no health threat.Publicado en: Atomic Spectroscopy.-- 2006, 27(3:80-85

  2. Multivariate optimization by exploratory analysis applied to the determination of microelements in fruit juice by inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Santos Froes, Roberta Eliane; Borges Neto, Waldomiro [Departamento de Quimica, Universidade Federal de Minas Gerais, Campus Pampulha, Cx Postal 702, Belo Horizonte, MG, 31270-901 (Brazil); Oliveira Couto e Silva, Nilton; Lopes Pereira Naveira, Rita [Fundacao Ezequiel Diaz, FUNED, Belo Horizonte, MG (Brazil); Nascentes, Clesia Cristina [Departamento de Quimica, Universidade Federal de Minas Gerais, Campus Pampulha, Cx Postal 702, Belo Horizonte, MG, 31270-901 (Brazil)], E-mail: clesia@qui.ufmg.br; Bento Borba da Silva, Jose [Departamento de Quimica, Universidade Federal de Minas Gerais, Campus Pampulha, Cx Postal 702, Belo Horizonte, MG, 31270-901 (Brazil)

    2009-06-15

    A method for the direct determination (without sample pre-digestion) of microelements in fruit juice by inductively coupled plasma optical emission spectrometry has been developed. The method has been optimized by a 2{sup 3} factorial design, which evaluated the plasma conditions (nebulization gas flow rate, applied power, and sample flow rate). A 1:1 diluted juice sample with 2% HNO{sub 3} (Tetra Packed, peach flavor) and spiked with 0.5 mg L{sup - 1} of Al, Ba, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Sb, Sn, and Zn was employed in the optimization. The results of the factorial design were evaluated by exploratory analysis (Hierarchical Cluster Analysis, HCA, and Principal Component Analysis, PCA) to determine the optimum analytical conditions for all elements. Central point condition differentiation (0.75 L min{sup - 1}, 1.3 kW, and 1.25 mL min{sup - 1}) was observed for both methods, Principal Component Analysis and Hierarchical Cluster Analysis, with higher analytical signal values, suggesting that these are the optimal analytical conditions. F and t-student tests were used to compare the slopes of the calibration curves for aqueous and matrix-matched standards. No significant differences were observed at 95% confidence level. The correlation coefficient was higher than 0.99 for all the elements evaluated. The limits of quantification were: Al 253, Cu 3.6, Fe 84, Mn 0.4, Zn 71, Ni 67, Cd 69, Pb 129, Sn 206, Cr 79, Co 24, and Ba 2.1 {mu}g L{sup - 1}. The spiking experiments with fruit juice samples resulted in recoveries between 80 and 120%, except for Co and Sn. Al, Cd, Pb, Sn and Cr could not be quantified in any of the samples investigated. The method was applied to the determination of several elements in fruit juice samples commercialized in Brazil.

  3. Multivariate optimization by exploratory analysis applied to the determination of microelements in fruit juice by inductively coupled plasma optical emission spectrometry

    Science.gov (United States)

    Froes, Roberta Eliane Santos; Neto, Waldomiro Borges; Silva, Nilton Oliveira Couto e.; Naveira, Rita Lopes Pereira; Nascentes, Clésia Cristina; da Silva, José Bento Borba

    2009-06-01

    A method for the direct determination (without sample pre-digestion) of microelements in fruit juice by inductively coupled plasma optical emission spectrometry has been developed. The method has been optimized by a 2 3 factorial design, which evaluated the plasma conditions (nebulization gas flow rate, applied power, and sample flow rate). A 1:1 diluted juice sample with 2% HNO 3 (Tetra Packed, peach flavor) and spiked with 0.5 mg L - 1 of Al, Ba, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Sb, Sn, and Zn was employed in the optimization. The results of the factorial design were evaluated by exploratory analysis (Hierarchical Cluster Analysis, HCA, and Principal Component Analysis, PCA) to determine the optimum analytical conditions for all elements. Central point condition differentiation (0.75 L min - 1 , 1.3 kW, and 1.25 mL min - 1 ) was observed for both methods, Principal Component Analysis and Hierarchical Cluster Analysis, with higher analytical signal values, suggesting that these are the optimal analytical conditions. F and t-student tests were used to compare the slopes of the calibration curves for aqueous and matrix-matched standards. No significant differences were observed at 95% confidence level. The correlation coefficient was higher than 0.99 for all the elements evaluated. The limits of quantification were: Al 253, Cu 3.6, Fe 84, Mn 0.4, Zn 71, Ni 67, Cd 69, Pb 129, Sn 206, Cr 79, Co 24, and Ba 2.1 µg L - 1 . The spiking experiments with fruit juice samples resulted in recoveries between 80 and 120%, except for Co and Sn. Al, Cd, Pb, Sn and Cr could not be quantified in any of the samples investigated. The method was applied to the determination of several elements in fruit juice samples commercialized in Brazil.

  4. An evaluation of microwave-assisted fusion and microwave-assisted acid digestion methods for determining elemental impurities in carbon nanostructures using inductively coupled plasma optical emission spectrometry

    KAUST Repository

    Patole, Shashikant P.

    2015-10-21

    It is common for as-prepared carbon nanotube (CNT) and graphene samples to contain remnants of the transition metals used to catalyze their growth; contamination may also leave other trace elemental impurities in the samples. Although a full quantification of impurities in as-prepared samples of carbon nanostructures is difficult, particularly when trace elements are intercalated or encapsulated within a protective layer of graphitic carbon, reliable information is essential for reasons such as quantifying the adulteration of physico-chemical properties of the materials and for evaluating environmental issues. Here, we introduce a microwave-based fusion method to degrade single- and double-walled CNTs and graphene nanoplatelets into a fusion flux thereby thoroughly leaching all metallic impurities. Subsequent dissolution of the fusion product in diluted hydrochloric and nitric acid allowed us to identify their trace elemental impurities using inductively coupled plasma optical emission spectrometry. Comparisons of the results from the proposed microwave-assisted fusion method against those of a more classical microwave-assisted acid digestion approach suggest complementarity between the two that ultimately could lead to a more reliable and less costly determination of trace elemental impurities in carbon nanostructured materials. Graphical abstract A method for the complete digestion of carbon nanostructures has been demonstrated. Photographs (on the left side) show zirconium crucibles containing SWCNTs with flux of Na2CO3 and K2CO3, before and after microwave fusion; (on the right side) the appearance of the final solutions containing dissolved samples, from microwave-assisted fusion and microwave-assisted acid digestion. These solutions were used for determining the trace elemental impurities by ICP‒OES.

  5. Assessment of heavy metal contamination in core sediment samples in Gulf of Izmir, Aegean Sea, Turkey (by inductively coupled plasma-optical emission spectrometry (ICP-OES))

    Science.gov (United States)

    Ünal Yumun, Zeki; Kam, Erol; Kurt, Dilek

    2017-04-01

    Heavy metal and radionuclide analysis studies are crucial in explaining biotic and abiotic interactions in ecosystems. This type of analysis is highly needed in environments such as coastal areas, gulfs or lakes where human activities are generally concentrated. Sediments are one of the best biological indicators for the environment since the pollution accumulates in the sediments by descent to the sea floor. In this study, sediments were collected from the Gulf of Izmir (Eastern Aegean Sea, Turkey) considering the accumulated points of domestic and industrial wastes to make an anthropogenic pollution analysis. The core sediments had different depths of 0.00-30.00 m at four different locations where Karsiyaka, Bayrakli, Incialti and Cesmealti in the Gulf of Izmir. The purpose of the study was determining Cd, Co, Cr, Cu, Mn, Ni, Pb, and Zn concentrations in the drilling samples to assess their levels and spatial distribution in crucial areas of the Aegean Sea by inductively coupled plasma-optical emission spectrometry (ICP-OES) with microwave digestion techniques. The heavy metal concentrations found in sediments varied for Cd:

  6. Sensitive determination of mercury in tap water by cloud point extraction pre-concentration and flow injection-cold vapor-inductively coupled plasma optical emission spectrometry

    Science.gov (United States)

    de Wuilloud, Jorgelina C. A.; Wuilloud, Rodolfo G.; Silva, María. F.; Olsina, Roberto A.; Martinez, Luis D.

    2002-02-01

    A pre-concentration and determination methodology for mercury at trace levels in water samples was developed. Cloud point extraction was successfully employed for the pre-concentration of mercury prior to inductively coupled plasma optical emission spectrometry coupled to a flow injection with cold vapor generation system. The mercury was extracted as mercury-2-(5-bromo-2-pyridylazo)-5-diethylaminophenol [Hg(II)-(5-Br-PADAP)] complex, at pH 9.2 mediated by micelles of the non-ionic surfactant polyethyleneglycolmono- p-nonylphenylether (PONPE 5). Cold vapor generation was developed from 100 μl of the extracted surfactant-rich phase by means of a stannous chloride (SnCl 2) solution as reluctant. An exhaustive study of the variables affecting the cloud point extraction with PONPE 5 and cold vapor mercury generation from the surfactant phase was performed. The 50-ml sample solution pre-concentration allowed us to raise an enrichment factor of 200-fold. The lower limit of detection obtained under the optimal conditions was 4 ng l -1. The precision for 10 replicate determinations at the 0.5-μg l -1 Hg level was 3.4% relative standard deviation (R.S.D.), calculated with the peak heights. The calibration graph using the pre-concentration system for mercury was linear with a correlation coefficient of 0.9998 at levels near the detection limits up to at least 50 μg l -1. The method was successfully applied to the determination of mercury in tap water samples.

  7. Determination of phosphorus and potassium in commercial inorganic fertilizers by inductively coupled plasma-optical emission spectrometry: single-laboratory validation.

    Science.gov (United States)

    Bartos, James M; Boggs, Barton L; Falls, J Harold; Siegel, Sanford A

    2014-01-01

    A two-part single-laboratory validation study was conducted for determination of the P and K content in commercial fertilizer materials by inductively coupled plasma-optical emission spectrometry (ICP-OES). While several methods exist for determination of P and K in fertilizer products, the main focus of this study was on ICP-OES determination, which offers several unique advantages. Fertilizer samples with consensus P and K values from the Magruder and Association of Fertilizer and Phosphate Chemists (AFPC) check sample programs were selected for this study. Validation materials ranging from 4.4 to 52.4% P205 (1.7 to 22.7% P) and 3 to 62% K20 (2.5 to 51.5% K) were utilized. Because all P and K compounds contained in fertilizer materials are not "available" for plants to use, this study was conducted in two parts. Part A focused on ammonium citrate-disodium EDTA as the extraction solvent, as it estimates the pool of fertilizer P and K that is considered available to plants. Part B focused on hydrochloric acid as the digestion solvent, as it estimates the total P and K content of the fertilizer product. Selectivity studies indicated that this method can have a high bias for fertilizer products containing sources of phosphite or organic P compared to gravimetric or colorimetric methods that measure just orthophosphate. Provided the analytical challenges outlined in this study are addressed, this method offers the potential for a quick, accurate, and safe alternative for determining the P and K content of commercial inorganic fertilizer materials.

  8. Introduction of organic/hydro-organic matrices in inductively coupled plasma optical emission spectrometry and mass spectrometry: A tutorial review. Part I. Theoretical considerations

    Energy Technology Data Exchange (ETDEWEB)

    Leclercq, Amélie, E-mail: amelie.leclercq@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Nonell, Anthony, E-mail: anthony.nonell@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Todolí Torró, José Luis, E-mail: jose.todoli@ua.es [Universidad de Alicante, Departamento de Quimica Analitica, Nutricion y Bromatología, Ap. de Correos, 99, 03080 Alicante (Spain); Bresson, Carole, E-mail: carole.bresson@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Vio, Laurent, E-mail: laurent.vio@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Vercouter, Thomas, E-mail: thomas.vercouter@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Chartier, Frédéric, E-mail: frederic.chartier@cea.fr [CEA Saclay, DEN, DANS, DPC, 91191 Gif-sur-Yvette (France)

    2015-07-23

    Highlights: • Tutorial review addressed to beginners or more experienced analysts. • Theoretical background of effects caused by organic matrices on ICP techniques. • Spatial distribution of carbon species and analytes in plasma. • Carbon spectroscopic and non-spectroscopic interferences in ICP. - Abstract: Due to their outstanding analytical performances, inductively coupled plasma optical emission spectrometry (ICP-OES) and mass spectrometry (ICP-MS) are widely used for multi-elemental measurements and also for isotopic characterization in the case of ICP-MS. While most studies are carried out in aqueous matrices, applications involving organic/hydro-organic matrices become increasingly widespread. This kind of matrices is introduced in ICP based instruments when classical “matrix removal” approaches such as acid digestion or extraction procedures cannot be implemented. Due to the physico-chemical properties of organic/hydro-organic matrices and their associated effects on instrumentation and analytical performances, their introduction into ICP sources is particularly challenging and has become a full topic. In this framework, numerous theoretical and phenomenological studies of these effects have been performed in the past, mainly by ICP-OES, while recent literature is more focused on applications and associated instrumental developments. This tutorial review, divided in two parts, explores the rich literature related to the introduction of organic/hydro-organic matrices in ICP-OES and ICP-MS. The present Part I, provides theoretical considerations in connection with the physico-chemical properties of organic/hydro-organic matrices, in order to better understand the induced phenomena. This focal point is divided in four chapters highlighting: (i) the impact of organic/hydro-organic matrices from aerosol generation to atomization/excitation/ionization processes; (ii) the production of carbon molecular constituents and their spatial distribution in the

  9. Introduction of organic/hydro-organic matrices in inductively coupled plasma optical emission spectrometry and mass spectrometry: A tutorial review. Part II. Practical considerations

    Energy Technology Data Exchange (ETDEWEB)

    Leclercq, Amélie, E-mail: amelie.leclercq@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Nonell, Anthony, E-mail: anthony.nonell@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Todolí Torró, José Luis, E-mail: jose.todoli@ua.es [Universidad de Alicante, Departamento de Quimica Analitica, Nutricion y Bromatología, Ap. de Correos, 99, 03080 Alicante (Spain); Bresson, Carole, E-mail: carole.bresson@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Vio, Laurent, E-mail: laurent.vio@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Vercouter, Thomas, E-mail: thomas.vercouter@cea.fr [CEA Saclay, DEN, DANS, DPC, SEARS, Laboratoire de développement Analytique Nucléaire Isotopique et Elémentaire, 91191 Gif-sur-Yvette (France); Chartier, Frédéric, E-mail: frederic.chartier@cea.fr [CEA Saclay, DEN, DANS, DPC, 91191 Gif-sur-Yvette (France)

    2015-07-23

    Graphical abstract: This tutorial review is dedicated to the analysis of organic/hydro-organic matrices by ICP techniques. A state-of-the-art focusing on sample introduction, relevant operating parameters optimization and analytical strategies for elemental quantification is provided. - Highlights: • Practical considerations to perform analyses in organic/hydro-organic matrices. • Description, benefits and drawbacks of recent introduction devices. • Optimization to improve plasma tolerance towards organic/hydro-organic matrices. • Analytical strategies for elemental quantification in organic/hydro-organic matrices. - Abstract: Inductively coupled plasma optical emission spectrometry (ICP-OES) and mass spectrometry (ICP-MS) are increasingly used to carry out analyses in organic/hydro-organic matrices. The introduction of such matrices into ICP sources is particularly challenging and can be the cause of numerous drawbacks. This tutorial review, divided in two parts, explores the rich literature related to the introduction of organic/hydro-organic matrices in ICP sources. Part I provided theoretical considerations associated with the physico-chemical properties of such matrices, in an attempt to understand the induced phenomena. Part II of this tutorial review is dedicated to more practical considerations on instrumentation, instrumental and operating parameters, as well as analytical strategies for elemental quantification in such matrices. Two important issues are addressed in this part: the first concerns the instrumentation and optimization of instrumental and operating parameters, pointing out (i) the description, benefits and drawbacks of different kinds of nebulization and desolvation devices and the impact of more specific instrumental parameters such as the injector characteristics and the material used for the cone; and, (ii) the optimization of operating parameters, for both ICP-OES and ICP-MS. Even if it is at the margin of this tutorial review

  10. Introduction of organic/hydro-organic matrices in inductively coupled plasma optical emission spectrometry and mass spectrometry: a tutorial review. Part I. Theoretical considerations.

    Science.gov (United States)

    Leclercq, Amélie; Nonell, Anthony; Todolí Torró, José Luis; Bresson, Carole; Vio, Laurent; Vercouter, Thomas; Chartier, Frédéric

    2015-07-23

    Due to their outstanding analytical performances, inductively coupled plasma optical emission spectrometry (ICP-OES) and mass spectrometry (ICP-MS) are widely used for multi-elemental measurements and also for isotopic characterization in the case of ICP-MS. While most studies are carried out in aqueous matrices, applications involving organic/hydro-organic matrices become increasingly widespread. This kind of matrices is introduced in ICP based instruments when classical "matrix removal" approaches such as acid digestion or extraction procedures cannot be implemented. Due to the physico-chemical properties of organic/hydro-organic matrices and their associated effects on instrumentation and analytical performances, their introduction into ICP sources is particularly challenging and has become a full topic. In this framework, numerous theoretical and phenomenological studies of these effects have been performed in the past, mainly by ICP-OES, while recent literature is more focused on applications and associated instrumental developments. This tutorial review, divided in two parts, explores the rich literature related to the introduction of organic/hydro-organic matrices in ICP-OES and ICP-MS. The present Part I, provides theoretical considerations in connection with the physico-chemical properties of organic/hydro-organic matrices, in order to better understand the induced phenomena. This focal point is divided in four chapters highlighting: (i) the impact of organic/hydro-organic matrices from aerosol generation to atomization/excitation/ionization processes; (ii) the production of carbon molecular constituents and their spatial distribution in the plasma with respect to analytes repartition; (iii) the subsequent modifications of plasma fundamental properties; and (iv) the resulting spectroscopic and non spectroscopic interferences. This first part of this tutorial review is addressed either to beginners or to more experienced scientists who are interested in the

  11. Total sulfur determination in gasoline, kerosene and diesel fuel using inductively coupled plasma optical emission spectrometry after direct sample introduction as detergent emulsions

    Energy Technology Data Exchange (ETDEWEB)

    Santelli, Ricardo Erthal [Departamento de Geoquimica, Universidade Federal Fluminense, Outeiro Sao Joao Batista s/n, Centro, Niteroi/RJ, 24020-150 (Brazil)], E-mail: santelli@geoq.uff.br; Padua Oliveira, Eliane [Departamento de Geoquimica, Universidade Federal Fluminense, Outeiro Sao Joao Batista s/n, Centro, Niteroi/RJ, 24020-150 (Brazil); Departamento de Engenharia Quimica e de Petroleo, Universidade Federal Fluminense, Rua Passos da Patria 156, Sao Domingos, Niteroi/RJ, 24210-230 (Brazil); Batista de Carvalho, Maria de Fatima [Centro de Pesquisas e Desenvolvimento da PETROBRAS, Avaliacao e Monitoramento Ambiental, Av. Horacio Macedo, 950, Cidade Universitaria, Rio de Janeiro/RJ, 21941-598 (Brazil); Almeida Bezerra, Marcos [Departamento de Geoquimica, Universidade Federal Fluminense, Outeiro Sao Joao Batista s/n, Centro, Niteroi/RJ, 24020-150 (Brazil); Universidade Estadual do Sudoeste da Bahia, Laboratorio de Quimica Analitica, Rua Jose Moreira Sobrinho s/n, Jequiezinho, Jequie/BA, 45206-190 (Brazil); Soares Freire, Aline [Departamento de Geoquimica, Universidade Federal Fluminense, Outeiro Sao Joao Batista s/n, Centro, Niteroi/RJ, 24020-150 (Brazil)

    2008-07-15

    Herein, we present the development of a procedure for the determination of total sulfur in petroleum-derived products (gasoline, kerosene and diesel fuel) employing inductively coupled plasma optical emission spectrometry (ICP OES). For this procedure, samples were prepared as emulsions that were made using concentrated nitric acid, Triton X-100, sample, and ultra pure water in proportions of 5/10/7/78% (v/v), respectively. Sample volumes were weighed because of the density differences, and oxygen was added to the sheat gas entrance of the ICP OES in order to decrease carbon deposition in the torch and to minimize background effects. A Doehlert design was applied as an experimental matrix to investigate the flow ratios of argon (sheat and plasma gas) and oxygen in relation to the signal-to-background ratio. A comparative study among the slopes of the analytical curves built in aqueous media, surfactant/HNO{sub 3}, and by spike addition for several sample emulsions indicates that a unique solution of surfactant in acidic media can be employed to perform the external calibration for analysis of the emulsions. The developed procedure allows for the determination of the total sulfur content in petroleum derivatives with a limit of detection (LOD) and limit of quantification (LOQ) of 0.72 and 2.4 {mu}g g{sup -1}, respectively. Precision values, expressed as the relative standard deviations (% RSD, n = 10) for 12 and 400 {mu}g g{sup -1}, were 2.2% and 1.3%, respectively. The proposed procedure was applied toward the determination of total sulfur in samples of gasoline, kerosene, and diesel fuel commercialized in the city of Niteroi/RJ, Brazil. The accuracy of the proposed method was evaluated by the determination of the total sulfur in three different standard reference materials (SRM): NIST 2723a (sulfur in diesel fuel oil), NIST 1616b (sulfur in kerosene), and NIST 2298 (sulfur in gasoline). The data indicate that the methodology can be successfully applied to these

  12. A methodology for quantifying trace elements in the exoskeletons of Florida stone crab (Menippe mercenaria) larvae using inductively coupled plasma optical emission spectrometry (ICP–OES)

    Science.gov (United States)

    Gravinese, Philip M.; Flannery, Jennifer A.; Toth, Lauren T.

    2016-11-23

    The larvae of the Florida stone crab, Menippe mercenaria, migrate through a variety of habitats as they develop and, therefore, experience a broad range of environmental conditions through ontogeny. Environmental variability experienced by the larvae may result in distinct elemental signatures within the exoskeletons, which could provide a tool for tracking the environmental history of larval stone crab populations. A method was developed to examine trace-element ratios, specifically magnesium-to-calcium (Mg/Ca) and strontium-to-calcium (Sr/Ca) ratios, in the exoskeletons of M. mercenaria larvae. Two developmental stages of stone crab larvae were analyzed—stage III and stage V. Specimens were reared in a laboratory environment under stable conditions to quantify the average ratios of Mg/Ca and Sr/Ca of larval stone crab exoskeletons and to determine if the ratios differed through ontogeny. The elemental compositions (Ca, Mg, and Sr) in samples of stage III larvae (n = 50 per sample) from 11 different broods (mean Sr/Ca = 5.916 ± 0.161 millimole per mole [mmol mol−1]; mean Mg/Ca = 218.275 ± 59.957 mmol mol−1) and stage V larvae (n = 10 per sample) from 12 different broods (mean Sr/Ca = 6.110 ± 0.300 mmol mol−1; mean Mg/Ca = 267.081 ± 67.211 mmol mol–1) were measured using inductively coupled plasma optical emission spectrometry (ICP–OES). The ratio of Sr/Ca significantly increased from stage III to stage V larvae, suggesting an ontogenic shift in Sr/Ca ratios between larval stages. The ratio of Mg/Ca did not change significantly between larval stages, but variability among broods was high. The method used to examine the trace-element ratios provided robust, highly reproducible estimates of Sr/Ca and Mg/Ca ratios in the larvae of M. mercenaria, demonstrating that ICP–OES can be used to determine the trace-element composition of chitinous organisms like the Florida stone crab.

  13. Ultrasound- and microwave-assisted extractions followed by hydride generation inductively coupled plasma optical emission spectrometry for lead determination in geological samples.

    Science.gov (United States)

    Welna, Maja; Borkowska-Burnecka, Jolanta; Popko, Malgorzata

    2015-11-01

    Followed the current idea of simplified sample pretratmet before analysis we evaluated the procedure for the determination of Pb in calcium-rich materials such as dolomites after ultrasound- or microwave- assisted extraction with diluted acids using hydride generation inductively coupled plasma optical emission spectrometry (HG-ICP-OES). Corresponding Pb hydride was generated in the reaction of an acidified sample solution with NaBH4 after pre-oxidation of Pb(II) to Pb(IV) by K3[Fe(CN)6]. Several chemical (acidic media: HCl, HNO3 or CH3COOH, concentration of the reductant as well as type and concentration of oxidazing agents) and physical (reagents flow rates, reaction coil length) parameters affecting the efficiency of plumbane formation were optimized in order to improve the detectability of Pb using HG-ICP-OES. Limitation of the method derived from the matrix effects was pointed out. Employing Pb separation by HG technique allows the significant reduction of interferences caused by sample matrix constituents (mainly Ca and Mg), nevertheless they could not be overcame at all, hence calibration based on the standard addition method was recommended for Pb quantification in dolomites. Under the selected conditions, i.e. 0.3 mol L(-1) HCl, HNO3 or CH3COOH, 1.5% NaBH4 and 3.0% K3[Fe(CN)6] the limits of detection (LODs) between 2.3-5.6 μg L(-1) (3.4-6.8 μg L(-1) considering matrix effects) and the precision below 5% were achieved. The accuracy of the procedure was verified by analysis of certified reference materials (NCS DC70308 (Carbonate Rock) and NIST 14000 (Bone Ash)) and recovery test with satisfactory results of Pb recoveries ranging between 94-108% (CRMs analysis) and 92-114% (standard addition method). The applicability of the proposed method was demonstrated by the determination of Pb in dolomites used by different fertiliser factories.

  14. Determination of metallic elements in natural and waste water by inductively coupled plasma-optical emission spectrometry (Icp-OES); Determinazione di specie metalliche in acque naturali e reflue mediante spettroscopia di emissione in sorgente al plasma (ICP-OES)

    Energy Technology Data Exchange (ETDEWEB)

    Petruzzelli, D. [Consiglio Nazionale delle Ricerche, Bari (Italy). Ist. di Ricerca sulle Acque; Bettinelli, M.; Spezia, S. [ENEL UML, Piacenza (Italy); Mastroianni, D.; Capri, S.; Pettine, M. [Consiglio Nazionale delle Ricerche, Rome (Italy). Ist. di Ricerca sulle Acque

    1998-12-31

    A method is described for multielement determination of 33 elements in liquids samples by inductively coupled plasma-optical emission spectrometry (Icp-OES). In this method the intensity of the light emitted at specific wavelengths from excited atoms and ions of a sample is measured and used to determine the concentrations of the element of interest. [Italiano] Viene descritto un metodo per la determinazione multielementare di 33 elementi in campioni liquidi basato sull`uso del plasma ottico. In questo metodo si misura l`intensita` della radiazione elettromagnetica emessa dagli atomi e ioni eccitati delle specie presenti nel campione.

  15. A rapid and practical strategy for the determination of platinum, palladium, ruthenium, rhodium, iridium and gold in large amounts of ultrabasic rock by inductively coupled plasma optical emission spectrometry combined with ultrasound extraction

    Science.gov (United States)

    Zhang, Gai; Tian, Min

    2015-04-01

    This proposed method regulated the determination of platinum, palladium, ruthenium, rhodium, iridium and gold in platinum-group ores by nickel sulfide fire assay—inductively coupled plasma optical emission spectrometry (ICP-OES) combined with ultrasound extraction for the first time. The quantitative limits were 0.013-0.023μg/g. The samples were fused to separate the platinum-group elements from matrix. The nickel sulfide button was then dissolved with hydrochloric acid and the insoluble platinum-group sulfide residue was dissolved with aqua regia by ultrasound bath and finally determined by ICP-OES. The proposed method has been applied into the determination of platinum-group element and gold in large amounts of ultrabasic rocks from the Great Dyke of Zimbabwe.

  16. Simultaneous determination of arsenic, cadmium, calcium, chromium, cobalt, copper, iron, lead, magnesium, manganese, molybdenum, nickel, selenium, and zinc in fertilizers by microwave acid digestion and inductively coupled plasma-optical emission spectrometry detection: single-laboratory validation of a modification and extension of AOAC 2006.03.

    Science.gov (United States)

    Webb, Sharon; Bartos, James; Boles, Rhonda; Hasty, Elaine; Thuotte, Ethel; Thiex, Nancy J

    2014-01-01

    A single-laboratory validation study was conducted for the simultaneous determination of arsenic, cadmium, calcium, cobalt, copper, chromium, iron, lead, magnesium, manganese, molybdenum, nickel, selenium, and zinc in all major types of commercial fertilizer products by microwave digestion and inductively coupled plasma-optical emission spectroscopy analysis. This validation study proposes an extension and modification of AOAC 2006.03. The extension is the inclusion of calcium, copper, iron, magnesium, manganese, and zinc, and the modification is incorporation of hydrochloric acid in the digestion system. This dual acid digestion utilizes both hydrochloric and nitric acids in a 3 to 9 mL volume ratio/100 mL. In addition to 15 of the 30 original validation materials used in the 2006.03 collaborative study, National Institute of Standards and Technology Standard Reference Material 695 and Magruder 2009-06 were incorporated as accuracy materials. The main benefits of this proposed method are a significant increase in laboratory efficiency when compared to the use of both AOAC Methods 965.09 and 2006.03 to achieve the same objective and an enhanced recovery of several metals.

  17. Internal standardization for the determination of cadmium, cobalt, chromium and manganese in saline produced water from petroleum industry by inductively coupled plasma optical emission spectrometry after cloud point extraction

    Energy Technology Data Exchange (ETDEWEB)

    Almeida Bezerra, Marcos [Departamento de Geoquimica, Universidade Federal Fluminense, Outeiro Sao Joao Batista s/n, Centro, Niteroi/RJ, 24020-150 (Brazil); Universidade Estadual do Sudoeste da Bahia, Departamento de Quimica e Exatas, Rua Jose Moreira Sobrinho s/n, Jequiezinho, Jequie/BA, 45206-190 (Brazil)], E-mail: mbezerra@uesb.br; Mitihiro do Nascimento Maeda, Sergio; Padua Oliveira, Eliane [Departamento de Geoquimica, Universidade Federal Fluminense, Outeiro Sao Joao Batista s/n, Centro, Niteroi/RJ, 24020-150 (Brazil); Fatima Batista de Carvalho, Maria de [Centro de Pesquisas e Desenvolvimento da PETROBRAS, Avaliacao e Monitoramento Ambiental, Av. Jequitiba, 950, Cidade Universitaria, Rio de Janeiro/RJ, 21941-598 (Brazil); Erthal Santelli, Ricardo [Departamento de Geoquimica, Universidade Federal Fluminense, Outeiro Sao Joao Batista s/n, Centro, Niteroi/RJ, 24020-150 (Brazil)

    2007-09-15

    In the present paper a procedure is proposed for the determination of traces of Cd, Co, Mn and Cr in petroleum industry produced water by inductively coupled plasma optical emission spectrometry. The procedure is based on cloud point extraction of these metals, as their dithizonate complexes, into the surfactant-rich phase of octylphenoxypolyethoxyethanol surfactant (Triton X-114). Extractions were carried out in solutions with salinities between 10 per mille and 70 per mille. Since residual salinity in the surfactant-rich phase caused differences in its transport to the plasma, yttrium was used as an internal standard to correct for this effect. The simultaneous metal extraction procedure was optimized by response surface methodology using a Doehlert design and desirability function. Enhancement factors of 21, 21, 9 and 19, along with limits of quantification of 0.093, 0.20, 0.73 and 1.2 {mu}g L{sup -1}, and precision expressed as relative standard deviation (n = 8, 20.0 {mu}g L{sup -1}) of 5.8, 1.2, 1.7 and 5.7% were obtained for Cd, Co, Mn and Cr, respectively. The accuracy was evaluated by spike recovery tests on the high salinity water samples with salinity of 40 and 63 per mille.

  18. Chemometric evaluation of Cd, Co, Cr, Cu, Ni (inductively coupled plasma optical emission spectrometry) and Pb (graphite furnace atomic absorption spectrometry) concentrations in lipstick samples intended to be used by adults and children.

    Science.gov (United States)

    Batista, Érica Ferreira; Augusto, Amanda dos Santos; Pereira-Filho, Edenir Rodrigues

    2016-04-01

    A method was developed for determining the concentrations of Cd, Co, Cr, Cu, Ni and Pb in lipstick samples intended to be used by adults and children using inductively coupled plasma optical emission spectrometry (ICP OES) and graphite furnace atomic absorption spectrometry (GF AAS) after treatment with dilute HNO3 and hot block. The combination of fractional factorial design and Desirability function was used to evaluate the ICP OES operational parameters and the regression models using Central Composite and Doehlert designs were calculated to stablish the best working condition for all analytes. Seventeen lipstick samples manufactured in different countries with different colors and brands were analyzed. Some samples contained high concentrations of toxic elements, such as Cr and Pb, which are carcinogenic and cause allergic and eczematous dermatitis. The maximum concentration detected was higher than the permissible safe limits for human use, and the samples containing these high metal concentrations were intended for use by children. Principal component analysis (PCA) was used as a chemometrics tool for exploratory analysis to observe the similarities between samples relative to the metal concentrations (a correlation between Cd and Pb was observed). Copyright © 2015 Elsevier B.V. All rights reserved.

  19. Internal standardization for the determination of cadmium, cobalt, chromium and manganese in saline produced water from petroleum industry by inductively coupled plasma optical emission spectrometry after cloud point extraction

    Science.gov (United States)

    Bezerra, Marcos Almeida; Mitihiro do Nascimento Maêda, Sérgio; Oliveira, Eliane Padua; de Fátima Batista de Carvalho, Maria; Santelli, Ricardo Erthal

    2007-09-01

    In the present paper a procedure is proposed for the determination of traces of Cd, Co, Mn and Cr in petroleum industry produced water by inductively coupled plasma optical emission spectrometry. The procedure is based on cloud point extraction of these metals, as their dithizonate complexes, into the surfactant-rich phase of octylphenoxypolyethoxyethanol surfactant (Triton X-114). Extractions were carried out in solutions with salinities between 10‰ and 70‰. Since residual salinity in the surfactant-rich phase caused differences in its transport to the plasma, yttrium was used as an internal standard to correct for this effect. The simultaneous metal extraction procedure was optimized by response surface methodology using a Doehlert design and desirability function. Enhancement factors of 21, 21, 9 and 19, along with limits of quantification of 0.093, 0.20, 0.73 and 1.2 μg L - 1 , and precision expressed as relative standard deviation ( n = 8, 20.0 μg L - 1 ) of 5.8, 1.2, 1.7 and 5.7% were obtained for Cd, Co, Mn and Cr, respectively. The accuracy was evaluated by spike recovery tests on the high salinity water samples with salinity of 40 and 63‰.

  20. Simultaneous preconcentration of copper, zinc, cadmium, and nickel in water samples by cloud point extraction using 4-(2-pyridylazo)-resorcinol and their determination by inductively coupled plasma optic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Edson Luiz, E-mail: edsonqmc@hotmail.com [Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Av. Centenario, 303, CP 96, 13416-000 Piracicaba, SP (Brazil); Santos Roldan, Paulo dos [Universidade Federal de Alagoas, Campus A.C. Simoes, Av. Lourival Melo Mota, Tabuleiro do Martins, CEP: 57072-970 AL (Brazil); Gine, Maria Fernanda [Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Av. Centenario, 303, CP 96, 13416-000 Piracicaba, SP (Brazil)

    2009-11-15

    A procedure for simultaneous separation/preconcentration of copper, zinc, cadmium, and nickel in water samples, based on cloud point extraction (CPE) as a prior step to their determination by inductively coupled plasma optic emission spectrometry (ICP-OES), has been developed. The analytes reacted with 4-(2-pyridylazo)-resorcinol (PAR) at pH 5 to form hydrophobic chelates, which were separated and preconcentrated in a surfactant-rich phase of octylphenoxypolyethoxyethanol (Triton X-114). The parameters affecting the extraction efficiency of the proposed method, such as sample pH, complexing agent concentration, buffer amount, surfactant concentration, temperature, kinetics of complexation reaction, and incubation time were optimized and their respective values were 5, 0.6 mmol L{sup -1}, 0.3 mL, 0.15% (w/v), 50 deg. C, 40 min, and 10 min for 15 mL of preconcentrated solution. The method presented precision (R.S.D.) between 1.3% and 2.6% (n = 9). The concentration factors with and without dilution of the surfactant-rich phase for the analytes ranged from 9.4 to 10.1 and from 94.0 to 100.1, respectively. The limits of detection (L.O.D.) obtained for copper, zinc, cadmium, and nickel were 1.2, 1.1, 1.0, and 6.3 {mu}g L{sup -1}, respectively. The accuracy of the procedure was evaluated through recovery experiments on aqueous samples.

  1. Cloud point extraction with/without chelating agent on-line coupled with inductively coupled plasma optical emission spectrometry for the determination of trace rare earth elements in biological samples

    Energy Technology Data Exchange (ETDEWEB)

    Li Yingjie [Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072 (China); Hu Bin, E-mail: binhu@whu.edu.cn [Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072 (China)

    2010-02-15

    The on-line incorporation of cloud point extraction (CPE) with/without 8-hydroxyquinoline (8-Ox) as chelating agent into flow injection analysis associated with inductively coupled plasma optical emission spectrometry (ICP-OES) for determining trace rare earth elements (REEs) is presented and evaluated. The significant parameters affecting on-line cloud point extraction of REEs such as sample pH, flow rate, 8-Ox concentration, Triton X-114 concentration were systematically studied. Under the optimized conditions, with the consumption of 3.0 mL sample solution, the limits of detection (3{sigma}) were ranged from 41.4 pg mL{sup -1} (Yb) to 448 pg mL{sup -1} (Gd) with relative standard deviations (RSDs) of 1.0% (Eu)-5.9% (Sm) for on-line CPE-ICP-OES with 8-Ox as chelating agent, and 69.0 pg mL{sup -1} (Sc) to 509.5 pg mL{sup -1} (Sm) with RSDs of 2.9% (Yb)-7.5% (Ho) for on-line CPE-ICP-OES without 8-Ox as chelating agent, respectively. The sample throughput of 17 samples h{sup -1} was obtained for both systems. The developed methods of on-line CPE-ICP-OES were validated by the analysis of certified reference material (GBW07605, tea leaves) and real biological samples of pig liver, Auricularia auricula and mushroom.

  2. Simultaneous preconcentration of copper, zinc, cadmium, and nickel in water samples by cloud point extraction using 4-(2-pyridylazo)-resorcinol and their determination by inductively coupled plasma optic emission spectrometry.

    Science.gov (United States)

    Silva, Edson Luiz; Roldan, Paulo dos Santos; Giné, Maria Fernanda

    2009-11-15

    A procedure for simultaneous separation/preconcentration of copper, zinc, cadmium, and nickel in water samples, based on cloud point extraction (CPE) as a prior step to their determination by inductively coupled plasma optic emission spectrometry (ICP-OES), has been developed. The analytes reacted with 4-(2-pyridylazo)-resorcinol (PAR) at pH 5 to form hydrophobic chelates, which were separated and preconcentrated in a surfactant-rich phase of octylphenoxypolyethoxyethanol (Triton X-114). The parameters affecting the extraction efficiency of the proposed method, such as sample pH, complexing agent concentration, buffer amount, surfactant concentration, temperature, kinetics of complexation reaction, and incubation time were optimized and their respective values were 5, 0.6 mmol L(-1), 0.3 mL, 0.15% (w/v), 50 degrees C, 40 min, and 10 min for 15 mL of preconcentrated solution. The method presented precision (R.S.D.) between 1.3% and 2.6% (n=9). The concentration factors with and without dilution of the surfactant-rich phase for the analytes ranged from 9.4 to 10.1 and from 94.0 to 100.1, respectively. The limits of detection (L.O.D.) obtained for copper, zinc, cadmium, and nickel were 1.2, 1.1, 1.0, and 6.3 microg L(-1), respectively. The accuracy of the procedure was evaluated through recovery experiments on aqueous samples.

  3. Restricted accessed material-copper(II) ion imprinted polymer solid phase extraction combined with inductively coupled plasma-optical emission spectrometry for the determination of free Cu(II) in urine and serum samples.

    Science.gov (United States)

    Cui, Chao; He, Man; Chen, Beibei; Hu, Bin

    2013-11-15

    A novel restricted accessed material (RAM)-Cu(II) ion imprinted polymer (IIP) was synthesized by the surface imprinted-emulsion method, and possessed a high selectivity to Cu(II) and good macromolecules exclusion property. And a novel method of RAM-IIP packed microcolumn solid phase extraction (SPE) combined with inductively coupled plasma-optical emission spectrometry (ICP-OES) was developed for the determination of trace free Cu(II) in human body fluids. Under the optimized conditions, the adsorption capacity of RAM-IIP for Cu(II) was 15.9 mg g(-1). With a preconcentration factor of 30, the limit of detection was 0.17 µg L(-1), and the relative standard deviation was 2.2% (n=7, c=1 µg L(-1)). The developed method was validated by the analysis of two Certified Reference Materials, and the determined values were in good agreement with the certified values. This method was also successfully applied for the direct analysis of free Cu(II) in human urine and serum samples. While the total Cu can be determined by the proposed method after microwave digestion. The concentrations of free Cu(II) were much lower than that of total Cu, indicating that Cu is mainly coordinated with macromolecules in these biological samples. From this point of view, the developed method exhibits application potential in speciation of free metal ions and metallic complex molecules in biological samples. © 2013 Elsevier B.V. All rights reserved.

  4. THz Emission Spectroscopy for THz Spintronics

    Science.gov (United States)

    Jarik Huisman, Thomas; Rasing, Theo

    2017-01-01

    Spintronics is used as the standard for the readout of magnetically stored data and also has commercial applications for writing data. The generation, control and detection of spin-polarized currents, spin-dependent electric transport, and pure spin currents on the subpicosecond (10-12 s) timescale are the next challenges in spintronics. Terahertz (THz, 1012 Hz) emission spectroscopy has proven to be an excellent tool for investigating these challenges. In this short review, we outline the functioning of this spectroscopic technique and its recent applications to spintronics.

  5. Inductively coupled plasma optical emission spectrometric determination of trace elements in sediments after sequential selective extraction: effects of reagents and major elements on the analytical signal.

    Science.gov (United States)

    Grotti, Marco; Ianni, Carmela; Frache, Roberto

    2002-07-19

    The interfering effects due to the reagents and matrix elements associated with a four step sequential extraction procedure on ICPOES determination of trace elements were investigated in a systematic way. The emission lines were selected in order to include the most interesting elements for environmental studies (Zn, Pb, Ni, Cr, V and Cu) and the concentrations ranged according with the values occurring in the real samples. In order to distinguish between chemical and physical interfering effects, the Mg 280.270-Mg 285.213 line intensity ratio was measured, in each condition. Both pneumatic and ultrasonic nebulization were considered for comparison. It was found that both the elements which constitute the sample and the reagents which are added during the sample preparation steps significantly influence the emission intensity of all the analytes, depending on the analytical concentration and the nebulization system. Generally, the signal variations were higher with ultrasonic nebulization. Concerning the interference mechanism, it was found that the effect of the major elements (Na, K, Mg, Ca, Al and Fe) is essentially related to a change of the aerosol generation and transport processes. Differently, acetic acid, ammonium acetate and hydroxylamine hydrochloride significantly improved the plasma excitation conditions, depending on their concentration. A change of the sample introduction efficiency due to the presence of these reagents was also evident. On the contrary, the effect of hydrochloric and nitric acid emerged to be related only to the processes occurring in the sample introduction system.

  6. High-Resolution Inductively Coupled Plasma Optical Emission Spectrometry for (234)U/(238)Pu Age Dating of Plutonium Materials and Comparison to Sector Field Inductively Coupled Plasma Mass Spectrometry.

    Science.gov (United States)

    Krachler, Michael; Alvarez-Sarandes, Rafael; Rasmussen, Gert

    2016-09-06

    Employing a commercial high-resolution inductively coupled plasma optical emission spectrometry (HR-ICP-OES) instrument, an innovative analytical procedure for the accurate determination of the production age of various Pu materials (Pu powder, cardiac pacemaker battery, (242)Cm heat source, etc.) was developed and validated. This undertaking was based on the fact that the α decay of (238)Pu present in the investigated samples produced (234)U and both mother and daughter could be identified unequivocally using HR-ICP-OES. Benefiting from the high spectral resolution of the instrument (U and (238)Pu were selectively and directly determined in the dissolved samples, i.e., without a chemical separation of the two analytes from each other. Exact emission wavelengths as well as emission spectra of (234)U centered around λ = 411.590 nm and λ = 424.408 nm are reported here for the first time. Emission spectra of the isotopic standard reference material IRMM-199, comprising about one-third each of (233)U, (235)U, and (238)U, confirmed the presence of (234)U in the investigated samples. For the assessment of the (234)U/(238)Pu amount ratio, the emission signals of (234)U and (238)Pu were quantified at λ = 424.408 nm and λ = 402.148 nm, respectively. The age of the investigated samples (range: 26.7-44.4 years) was subsequently calculated using the (234)U/(238)Pu chronometer. HR-ICP-OES results were crossed-validated through sector field inductively coupled plasma mass spectrometry (SF-ICPMS) analysis of the (234)U/(238)Pu amount ratio of all samples applying isotope dilution combined with chromatographic separation of U and Pu. Available information on the assumed ages of the analyzed samples was consistent with the ages obtained via the HR-ICP-OES approach. Being based on a different physical detection principle, HR-ICP-OES provides an alternative strategy to the well-established mass spectrometric approach and thus effectively adds to the quality assurance of (234)U

  7. Mid infrared emission spectroscopy of carbon plasma

    Science.gov (United States)

    Nemes, Laszlo; Brown, Ei Ei; Yang, Clayton S.-C.; Hommerich, Uwe

    2017-01-01

    Mid infrared time-resolved emission spectra were recorded from laser-induced carbon plasma. These spectra constitute the first study of carbon materials LIB spectroscopy in the mid infrared range. The carbon plasma was induced using a Q-switched Nd: YAG laser. The laser beam was focused to high purity graphite pellets mounted on a translation stage. Mid infrared emission from the plasma in an atmospheric pressure background gas was detected by a cooled HgCdTe detector in the range 4.4-11.6 μm, using long-pass filters. LIB spectra were taken in argon, helium and also in air. Despite a gate delay of 10 μs was used there were strong backgrounds in the spectra. Superimposed on this background broad and noisy emission bands were observed, the form and position of which depended somewhat on the ambient gas. The spectra were digitally smoothed and background corrected. In argon, for instance, strong bands were observed around 4.8, 6.0 and 7.5 μm. Using atomic spectral data by NIST it could be concluded that carbon, argon, helium and nitrogen lines from neutral and ionized atoms are very weak in this spectral region. The width of the infrared bands supports molecular origin. The infrared emission bands were thus compared to vibrational features of carbon molecules (excluding C2) of various sizes on the basis of previous carbon cluster infrared absorption and emission spectroscopic analyses in the literature and quantum chemical calculations. Some general considerations are given about the present results.

  8. Mid infrared emission spectroscopy of carbon plasma.

    Science.gov (United States)

    Nemes, Laszlo; Brown, Ei Ei; S-C Yang, Clayton; Hommerich, Uwe

    2017-01-05

    Mid infrared time-resolved emission spectra were recorded from laser-induced carbon plasma. These spectra constitute the first study of carbon materials LIB spectroscopy in the mid infrared range. The carbon plasma was induced using a Q-switched Nd: YAG laser. The laser beam was focused to high purity graphite pellets mounted on a translation stage. Mid infrared emission from the plasma in an atmospheric pressure background gas was detected by a cooled HgCdTe detector in the range 4.4-11.6μm, using long-pass filters. LIB spectra were taken in argon, helium and also in air. Despite a gate delay of 10μs was used there were strong backgrounds in the spectra. Superimposed on this background broad and noisy emission bands were observed, the form and position of which depended somewhat on the ambient gas. The spectra were digitally smoothed and background corrected. In argon, for instance, strong bands were observed around 4.8, 6.0 and 7.5μm. Using atomic spectral data by NIST it could be concluded that carbon, argon, helium and nitrogen lines from neutral and ionized atoms are very weak in this spectral region. The width of the infrared bands supports molecular origin. The infrared emission bands were thus compared to vibrational features of carbon molecules (excluding C2) of various sizes on the basis of previous carbon cluster infrared absorption and emission spectroscopic analyses in the literature and quantum chemical calculations. Some general considerations are given about the present results.

  9. Investigations on the use of pneumatic cross-flow nebulizers with dual solution loading including the correction of matrix effects in elemental determinations by inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Bauer, Mathieu [Institute for Inorganic and Applied Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, D-20146 Hamburg (Germany); Broekaert, Jose A.C. [Institute for Inorganic and Applied Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, D-20146 Hamburg (Germany)], E-mail: jose.broekaert@chemie.uni-hamburg.de

    2007-02-15

    The use of a so-called trihedral and a T-shaped cross-flow pneumatic nebulizer with dual solution loading for inductively coupled plasma optical emission spectrometry has been studied. By these devices analyte clouds from two solutions can be mixed during the aerosol generation step. For both nebulizers the correction of matrix effects using internal standardization and standard addition calibration in an on-line way was investigated and compared to elemental determinations using a conventional cross-flow nebulizer and calibration with synthetic standard solutions without matrix matching. A significant improvement of accuracy, both for calibration with internal standardization and standard addition, was obtained in the case of four synthetic solutions containing each 40 mmol L{sup -1} Na, K, Rb and Ba as matrix elements and 300 {mu}g L{sup -1} Cd, Co, Cr, Cu, Fe, Mn, Ni and Pb as analytes. Calibration by standard addition in the case of dual solution loading has been shown to be very useful in the determination of elements at minor and trace levels in steel and alumina reference materials. The results of analysis for minor concentrations of Cr, Cu and Ni in steel as well as for Ca, Fe, Ga, Li, Mg, Mn, Na, Si and Zn in alumina powder certified reference materials subsequent to sample dissolution were found to be in good agreement with the certificates. Limits of detection were found to be only slightly above those for a conventional cross-flow nebulizer and a precision better than 3% was realized with both novel nebulizers.

  10. Analysis of metals and phosphorus in biodiesel B100 from different feedstock using a Flow Blurring® multinebulizer in inductively coupled plasma-optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Avila Orozco, Francisco D. [Lab. FIA, Sección Química Analítica, INQUISUR (UNS-CONICET), Universidad Nacional del Sur, Avenida Alem 1253, B8000CPB, Bahía Blanca (Argentina); Kovachev, Nikolay; Aguirre Pastor, Miguel Ángel [Dpto. Química Analítica, Nutrición y Bromatología e Instituto Universitario de Materiales, Facultad de Ciencias, Universidad de Alicante, Apdo. 99, Alicante (Spain); Domini, Claudia E.; Fernández Band, Beatriz S. [Lab. FIA, Sección Química Analítica, INQUISUR (UNS-CONICET), Universidad Nacional del Sur, Avenida Alem 1253, B8000CPB, Bahía Blanca (Argentina); Canals Hernández, Antonio, E-mail: a.canals@ua.es [Dpto. Química Analítica, Nutrición y Bromatología e Instituto Universitario de Materiales, Facultad de Ciencias, Universidad de Alicante, Apdo. 99, Alicante (Spain)

    2014-05-01

    Highlights: • The elemental analysis of biodiesel by the proposed method is simple and fast. • Two-nozzles Flow Blurring® nebulizer allow to reduce the spectral interferences. • Two-nozzles Flow Blurring® nebulizer avoid the formation of carbon deposits. • The analysis may be carried out without any sample pretreatment. Abstract: A simple and fast method for determining the content of Na, K, Ca, Mg, P, and 20 heavy metals in biodiesel samples with inductively coupled plasma optical emission spectrometry (ICP OES) using a two-nozzle Flow Blurring® multinebulizer prototype and on-line internal standard calibration, are proposed. The biodiesel samples were produced from different feedstock such as sunflower, corn, soybean and grape seed oils, via a base catalyst transesterification. The analysis was carried out without any sample pretreatment. The standards and samples were introduced through one of the multinebulizer nozzles, while the aqueous solution containing yttrium as an internal standard was introduced through the second nozzle. Thus, the spectral interferences were compensated and the formation of carbon deposits on the ICP torch was prevented. The determination coefficients (R²) were greater than 0.99 for the studied analytes, in the range 0.21–14.75 mg kg⁻¹. Short-term and long-term precisions were estimated as relative standard deviation. These were acceptable, their values being lower than 10%. The LOQ for major components such as Ca, K, Mg, Na, and P, were within a range between 4.9 ng g⁻¹ for Mg (279.553 nm) and 531.1 ng g⁻¹ for Na (588.995 nm), and for the other 20 minor components they were within a range between 1.1 ng g⁻¹ for Ba (455.403 nm) and 2913.9 ng g⁻¹ for Pb (220.353 nm). Recovery values ranged between 95% and 106%.

  11. Understanding the effects of potassium ferricyanide on lead hydride formation in tetrahydroborate system and its application for determination of lead in milk using hydride generation inductively coupled plasma optical emission spectrometry.

    Science.gov (United States)

    Deng, Biyang; Xu, Xiangshu; Xiao, Yan; Zhu, Pingchuan; Wang, Yingzi

    2015-01-01

    To understand the formation of plumbane in the Pb(II)-NaBH4-K3Fe(CN)6 system, the intermediate products produced in the reaction of lead(II) and NaBH4 in the presence of K3Fe(CN)6 were studied. The produced plumbane and elemental lead were measured through continuous flow hydride generation (HG)-inductively coupled plasma optical emission spectrometry (ICP OES) and X-ray diffraction spectrometry techniques, respectively. Based on the experimental results, the explanations can be depicted in the following steps: (1) plumbane and black lead sediment (black Pb) are formed in the reaction of lead(II) and NaBH4; (2) the black Pb is oxidized by K3Fe(CN)6 to form Pb2[Fe(CN)6], which further reacts with NaBH4 to form more plumbane and black Pb; and (3) another round starts in which the produced black Pb from the step 2 is then oxidized continuously by K3Fe(CN)6 to form more Pb2[Fe(CN)6] complex, which would produce more plumbane. In short, the black Pb and Pb2[Fe(CN)6] complex are the key intermediate products for the formation of plumbane in the Pb(II)-NaBH4-K3Fe(CN)6 system. Based on the enhancement effect of potassium ferricyanide and potassium ferrocyanide, a method was developed to analyze lead in milk with HG-ICP OES technique. The detection limit of the method was observed as 0.081 μg L(-1). The linearity range of lead was found between 0.3 and 50,000 μg L(-1) with correlation coefficient of 0.9993. The recovery of lead was determined as 97.6% (n=5) for adding 10 μg L(-1) lead into the milk sample.

  12. Simultaneous determination of 11 trace elements in coal by inductively coupled plasma-optical emission spectrometry%ICP-OES法同时测定煤中11种微量元素

    Institute of Scientific and Technical Information of China (English)

    吕鑫磊

    2015-01-01

    To quickly determine microelements of coal in batch,the coal sample was ashed first at high temperature,then the product was dissolved by the mixture of HCl,HF and HClO4 ,the third step was to extract the microelements with HCl. The microelements which were Ga,Th,V,P,Cu,Co,Ni,Zn,Pb,Cr,Cd were determined with ICP-OES (Inductively Coupled Plasma-Optical Emission Spectrometry). With reasonable sample dissolution methods,radio-frequency power,analytical spectral line and experimental data,the influence of spec-tral interference on determination was eliminated by off-peak background deduction method, meanwhile, the 11 kinds of microelements could be determined by ICP-OES at the same time. The detection limits for the elements was 0. 03~1. 17 μg/g. The method was applied to the determination of 11 microelements in Soil National Standard Reference Materials and the results were in agreement with certified val-ues with precision of 0. 32% ~3. 19% RSD (n=11).%为实现煤中多种微量元素的批量快速测定,煤样经高温灰化、盐酸-氢氟酸-高氯酸三元体系溶解、盐酸提取后,使用电感耦合等离子体发射光谱( ICP-OES )同时测定煤中镓钍钒磷铜钴镍锌铅铬镉11种微量元素. 在对样品分解方法、射频功率、分析谱线和积分点数合理选择的基础上,通过离峰扣背景法消除了各种光谱干扰对测定的影响,建立了采用ICP-OES同时测定煤中镓钍钒磷铜钴镍锌铅铬镉 11 种微量元素的实验方法. 方法检出限为 0. 03 ~1. 17 μg/g,方法精密度( n=11 ) 0. 32% ~3. 19%,土壤国家标准物质的分析测定值与标准值吻合较好. 与传统化学方法相比,该方法快速准确,提高了分析效率,满足煤质分析的一般要求.

  13. Análise de suspensões de argilas por espectrometria de emissão óptica com plasma induzido com configuração axial Clay slurries analysis using inductively coupled plasma optical emission spectrometry with axial view configuration

    Directory of Open Access Journals (Sweden)

    Cíntia S. Silva

    2002-12-01

    Full Text Available The goal of this study was to evaluate the feasibility of direct introduction of clay slurries in an inductively coupled plasma optical emission spectrometer with axial view configuration. Calibration was performed using a certified reference material with a mean particle size of 13 µm (IPT-42 and the analytical curve was applied for quantification of two others reference materials (IPT-28 and IPT-32 and four samples. It was demonstrated that the analytical curve thus obtained was not completely suitable for IPT-28 and samples due to different mineralogical phases determined by X-ray diffraction. After considering this effect, it was possible for most elements to obtain results in agreement with certified values or with values obtained by a conventional technique at a 95% confidence level. It was demonstrated that the ICP-OES with axial view configuration did not present any incompatibility with the direct introduction of a complex inorganic suspension.

  14. Decomposição de argilas em forno de microondas e determinação simultânea dos seus constituintes principais por espectrometria de emissão óptica em plasma indutivamente acoplado Analysis of clays by inductively coupled plasma optical emission spectrometry after closed-vessel microwave-assisted acid decomposition

    Directory of Open Access Journals (Sweden)

    Claudineia R. Silva

    2005-02-01

    Full Text Available In this work a closed-vessel microwave-assisted acid decomposition procedure for clays was developed. Aluminum, Ca, Fe, K, Mg, Na, Si, and Ti were determined in clay digestates by inductively coupled plasma optical emission spectrometry. The most critical parameter for total decomposition of clays was the composition of the reagent mixture. The applied power and the heating time exerted a less critical influence. Best decomposition conditions were attained using a reagent mixture containing 4 mL aqua regia plus 3 mL HF and the heating program was implemented in 12 min. The accuracy of the results was demonstrated using two standard reference materials and a paired t-test showed a good agreement between determined and certified values at a 95% confidence level.

  15. Liquid-Arc/Spark-Excitation Atomic-Emission Spectroscopy

    Science.gov (United States)

    Schlagen, Kenneth J.

    1992-01-01

    Constituents of solutions identified in situ. Liquid-arc/spark-excitation atomic-emission spectroscopy (LAES) is experimental variant of atomic-emission spectroscopy in which electric arc or spark established in liquid and spectrum of light from arc or spark analyzed to identify chemical elements in liquid. Observations encourage development of LAES equipment for online monitoring of process streams in such industries as metal plating, electronics, and steel, and for online monitoring of streams affecting environment.

  16. Determination of Serum Lithium by Flame Emission Spectroscopy

    Directory of Open Access Journals (Sweden)

    R. Nafissy

    1976-07-01

    Full Text Available Lithum can be de termined both by atomic absorption spectroscopy andflame emission spectroscopy. We have used the later method with a Zeiss Model pMQlI spectro photometer fitt ed with ante-chamber atomizer and a potensiome rric line recorder. Accurate ana lysis for the clement was acco mplished due to a sophisracared measuring instrument.

  17. Understanding the effects of potassium ferricyanide on lead hydride formation in tetrahydroborate system and its application for determination of lead in milk using hydride generation inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Deng, Biyang, E-mail: dengby16@163.com; Xu, Xiangshu; Xiao, Yan; Zhu, Pingchuan; Wang, Yingzi

    2015-01-01

    Highlights: • Proposed a novel explanation for plumbane generation. • Expounded the role of K{sub 3}Fe(CN){sub 6} in plumbane generation. • Clarified the controversial aspects in the mechanism of K{sub 3}Fe(CN){sub 6} enhancement. • Used X-ray diffractometry to analyze the intermediates. • Developed a method to analyze lead in milk using K{sub 3}Fe(CN){sub 6} and K{sub 4}Fe(CN){sub 6} as new additives. - Absract: To understand the formation of plumbane in the Pb{sup II}-NaBH{sub 4}-K{sub 3}Fe(CN){sub 6} system, the intermediate products produced in the reaction of lead(II) and NaBH{sub 4} in the presence of K{sub 3}Fe(CN){sub 6} were studied. The produced plumbane and elemental lead were measured through continuous flow hydride generation (HG)-inductively coupled plasma optical emission spectrometry (ICP OES) and X-ray diffraction spectrometry techniques, respectively. Based on the experimental results, the explanations can be depicted in the following steps: (1) plumbane and black lead sediment (black Pb) are formed in the reaction of lead(II) and NaBH{sub 4}; (2) the black Pb is oxidized by K{sub 3}Fe(CN){sub 6} to form Pb{sub 2}[Fe(CN){sub 6}], which further reacts with NaBH{sub 4} to form more plumbane and black Pb; and (3) another round starts in which the produced black Pb from the step 2 is then oxidized continuously by K{sub 3}Fe(CN){sub 6} to form more Pb{sub 2}[Fe(CN){sub 6}] complex, which would produce more plumbane. In short, the black Pb and Pb{sub 2}[Fe(CN){sub 6}] complex are the key intermediate products for the formation of plumbane in the Pb{sup II}-NaBH{sub 4}-K{sub 3}Fe(CN){sub 6} system. Based on the enhancement effect of potassium ferricyanide and potassium ferrocyanide, a method was developed to analyze lead in milk with HG-ICP OES technique. The detection limit of the method was observed as 0.081 μg L{sup −1}. The linearity range of lead was found between 0.3 and 50,000 μg L{sup −1} with correlation coefficient of 0

  18. Spectroscopy of unusual emission-line stars

    Science.gov (United States)

    Bopp, Bernard W.

    1988-01-01

    New spectroscopic observations are reported for ten stars that have been identified in the literature as having H-alpha emission with suspected F, G, or K spectral types. Three of the stars are shown to be BE stars, two are confirmed as early-type supergiants, three show composite (F or K + B) spectra, one is a 'post-T Tauri' star, and one is an ordinary F star without emission.

  19. Determinação de elementos essenciais maiores e traço em queijos por espectrometria de emissão atômica com plasma de argônio induzido após digestão parcial Determination of minerals and trace elements in cheese by inductively-coupled plasma optical emission spectrometry after partial digestion

    Directory of Open Access Journals (Sweden)

    Carmen Silvia Kira

    2007-09-01

    Full Text Available Concentrações de Ca, Cr, Cu, Fe, K, Mg, Mn, Na, P e Zn foram determinadas em amostras de quatro tipos de queijo (mussarela, minas, prato e parmesão por espectrometria de emissão atômica com plasma de argônio acoplado indutivamente após dissolução parcial (hidrólise com HCl e total da matéria orgânica (digestão por via seca. As concentrações da maioria dos elementos essenciais maiores e traço, usando o método de dissolução parcial, foram consideradas estatisticamente iguais às obtidas com o método de dissolução total da matéria orgânica, demonstrando a potencialidade da digestão parcial em análises de rotina.Concentrations of Ca, Cr, Cu, Fe, K, Mg, Mn, Na, P and Zn in four different types of cheese (mozzarella, white cheese, prato and parmesan were analyzed by inductively-coupled plasma optical emission spectrometry (ICP-OES after partial digestion (HCl hydrolysis and total digestion of organic matter (dry ashing. The results obtained for most of the elements analyzed here by the partial digestion (HCl hydrolysis and dry ashing methods were found to be statistically congruent, demonstrating the promising potential of the partial digestion method in routine analyses.

  20. [Spectroscopy technique and ruminant methane emissions accurate inspecting].

    Science.gov (United States)

    Shang, Zhan-Huan; Guo, Xu-Sheng; Long, Rui-Jun

    2009-03-01

    The increase in atmospheric CH4 concentration, on the one hand through the radiation process, will directly cause climate change, and on the other hand, cause a lot of changes in atmospheric chemical processes, indirectly causing climate change. The rapid growth of atmospheric methane has gained attention of governments and scientists. All countries in the world now deal with global climate change as an important task of reducing emissions of greenhouse gases, but the need for monitoring the concentration of methane gas, in particular precision monitoring, can be scientifically formulated to provide a scientific basis for emission reduction measures. So far, CH4 gas emissions of different animal production systems have received extensive research. The methane emission by ruminant reported in the literature is only estimation. This is due to the various factors that affect the methane production in ruminant, there are various variables associated with the techniques for measuring methane production, the techniques currently developed to measure methane are unable to accurately determine the dynamics of methane emission by ruminant, and therefore there is an urgent need to develop an accurate method for this purpose. Currently, spectroscopy technique has been used and is relatively a more accurate and reliable method. Various spectroscopy techniques such as modified infrared spectroscopy methane measuring system, laser and near-infrared sensory system are able to achieve the objective of determining the dynamic methane emission by both domestic and grazing ruminant. Therefore spectroscopy technique is an important methane measuring technique, and contributes to proposing reduction methods of methane.

  1. Emission spectroscopy analysis during Nopal cladodes dethorning by laser ablation

    Science.gov (United States)

    Peña-Díaz, M.; Ponce, L.; Arronte, M.; Flores, T.

    2007-04-01

    Optical emission spectroscopy of the pulsed laser ablation of spines and glochids from Opuntia (Nopal) cladodes was performed. Nopal cladodes were irradiated with Nd:YAG free-running laser pulses on their body, glochids and spines. Emission spectroscopy analyses in the 350-1000 nm region of the laser induced plasma were made. Plasma plume evolution characterization, theoretical calculations of plasma plume temperature and experiments varying the processing atmosphere showed that the process is dominated by a thermally activated combustion reaction which increases the dethorning process efficiency. Therefore, appropriate laser pulse energy for minimal damage of cladodes body and in the area beneath glochids and spines can be obtained.

  2. Emission spectroscopy analysis during Nopal cladodes dethorning by laser ablation

    Energy Technology Data Exchange (ETDEWEB)

    Pena-Diaz, M; Ponce, L; Arronte, M; Flores, T [Laboratorio TecnologIa Laser, CICATA-IPN, Unidad Altamira, Carretera Tampico-Puerto Ind. Altamira, 89600, TAMPS (Mexico)

    2007-04-15

    Optical emission spectroscopy of the pulsed laser ablation of spines and glochids from Opuntia (Nopal) cladodes was performed. Nopal cladodes were irradiated with Nd:YAG free-running laser pulses on their body, glochids and spines. Emission spectroscopy analyses in the 350-1000 nm region of the laser induced plasma were made. Plasma plume evolution characterization, theoretical calculations of plasma plume temperature and experiments varying the processing atmosphere showed that the process is dominated by a thermally activated combustion reaction which increases the dethorning process efficiency. Therefore, appropriate laser pulse energy for minimal damage of cladodes body and in the area beneath glochids and spines can be obtained.

  3. A novel method for fast enrichment and monitoring of hexavalent and trivalent chromium at the ppt level with modified silica MCM-41 and its determination by inductively coupled plasma optical emission spectrometry

    Directory of Open Access Journals (Sweden)

    Ganjali Mohammad Reza

    2006-01-01

    Full Text Available Chromium(III at the ng L-1 level was extracted using partially silylated MCM-41 modified by a tetraazamacrocyclic compound (TAMC and determined by inductively coupled plasma optical emision spectrometry (ICP OES. The extraction time and efficiency, pH and flow rate, type and minimum amount of stripping acid, and break- through volume were investigated. The method's enrichment factor and detection limit are 300 and 45.5 pg mL-1, respectively. The maximum capacity of the 10 mg of modified silylated MCM-41 was found to be 400.5?4.7 µg for Cr(III. The method was applied to the determination of Cr(III and Cr(VI in the wastewater of the chromium electroplating industry and in environmental and biological samples (black tea, hot and black pepper.

  4. Optimally enhanced optical emission in laser-induced breakdown spectroscopy by combining spatial confinement and dual-pulse irradiation.

    Science.gov (United States)

    Guo, L B; Zhang, B Y; He, X N; Li, C M; Zhou, Y S; Wu, T; Park, J B; Zeng, X Y; Lu, Y F

    2012-01-16

    In laser-induced breakdown spectroscopy (LIBS), a pair of aluminum-plate walls were used to spatially confine the plasmas produced in air by a first laser pulse (KrF excimer laser) from chromium (Cr) targets with a second laser pulse (Nd:YAG laser at 532 nm, 360 mJ/pulse) introduced parallel to the sample surface to re-excite the plasmas. Optical emission enhancement was achieved by combing the spatial confinement and dual-pulse LIBS (DP-LIBS), and then optimized by adjusting the distance between the two walls and the interpulse delay time between both laser pulses. A significant enhancement factor of 168.6 for the emission intensity of the Cr lines was obtained at an excimer laser fluence of 5.6 J/cm(2) using the combined spatial confinement and DP-LIBS, as compared with an enhancement factor of 106.1 was obtained with DP-LIBS only. The enhancement mechanisms based on shock wave theory and reheating in DP-LIBS are discussed.

  5. Recent development of plasma optical systems (invited)

    Energy Technology Data Exchange (ETDEWEB)

    Goncharov, A. A., E-mail: gonchar@iop.kiev.ua [Institute of Physics, National Academy of Science, Kiev 03028 (Ukraine)

    2016-02-15

    The article devotes a brief description of the recent development and current status of an ongoing research of plasma optical systems based on the fundamental plasma optical idea magnetic electron isolation, equipotentialization magnetic field lines, and the axi-symmetric cylindrical electrostatic plasma lens (PL) configuration. The experimental, theoretical, and simulation investigations have been carried out over recent years collaboratively between IP NASU (Kiev), LBNL (Berkeley, USA), and HCEI RAS (Tomsk). The crossed electric and magnetic fields inherent the PL configuration that provides the attractive method for establishing a stable plasma discharge at low pressure. Using PL configuration, several high reliability plasma devices were developed. These devices are attractive for many high-tech applications.

  6. Measuring the Silver Composition of Nanocolloids by Inductively Coupled Plasma-Optical Emission Spectroscopy: A Laboratory Experiment for Chemistry and Engineering Students

    Science.gov (United States)

    Brittle, Seth W.; Baker, Joshua D.; Dorney, Kevin M.; Dagher, Jessica M.; Ebrahimian, Tala; Higgins, Steven R.; Pavel Sizemore, Ioana E.

    2015-01-01

    The increased worldwide exploitation of nanomaterials has reinforced the importance of introducing nanoscale aspects into the undergraduate and graduate curriculum. To meet this need, a novel nano-laboratory module was developed and successfully performed by science and engineering students. The main goal of the experiment was to accurately…

  7. Laser-induced breakdown spectroscopy for quantification of heavy metals in soils and sediments

    CSIR Research Space (South Africa)

    Ambushe, AA

    2010-09-01

    Full Text Available Laser-induced breakdown spectroscopy (LIBS) will be used to determine the contents of heavy metals in soils and sediments. LIBS results will be compared with the results obtained by inductively coupled plasma-optical emission spectrometry (ICP...

  8. Plant species discrimination using emissive thermal infrared imaging spectroscopy

    Science.gov (United States)

    Rock, Gilles; Gerhards, Max; Schlerf, Martin; Hecker, Christoph; Udelhoven, Thomas

    2016-12-01

    Discrimination of plant species in the optical reflective domain is somewhat limited by the similarity of their reflectance spectra. Spectral characteristics in the visible to shortwave infrared (VSWIR) consist of combination bands and overtones of primary absorption bands, situated in the Thermal Infrared (TIR) region and therefore resulting in broad spectral features. TIR spectroscopy is assumed to have a large potential for providing complementary information to VSWIR spectroscopy. So far, in the TIR, plants were often considered featureless. Recently and following advances in sensor technology, plant species were discriminated based on specific emissivity signatures by Ullah et al. (2012) using directional-hemispherical reflectance (DHR) measurements in the laboratory. Here we examine if an accurate discrimination of plant species is equally possible using emissive thermal infrared imaging spectroscopy, an explicit spatial technique that is faster and more flexible than non-imaging measurements. Hyperspectral thermal infrared images were acquired in the 7.8⿿11.56 μm range at 40 nm spectral resolution (@10 μm) using a TIR imaging spectrometer (Telops HyperCam-LW) on seven plants each, of eight different species. The images were radiometrically calibrated and subjected to temperature and emissivity separation using a spectral smoothness approach. First, retrieved emissivity spectra were compared to laboratory reference spectra and then subjected to species discrimination using a random forest classifier. Second, classification results obtained with emissivity spectra were compared to those obtained with VSWIR reflectance spectra that had been acquired from the same leaf samples. In general, the mean emissivity spectra measured by the TIR imaging spectrometer showed very good agreement with the reference spectra (average Nash-Sutcliffe-Efficiency Index = 0.64). In species discrimination, the resulting accuracies for emissivity spectra are highly dependent on

  9. Spectroscopy of an unusual emission line M star

    Science.gov (United States)

    Schneider, Donald P.; Greenstein, Jesse L.; Schmidt, Maarten; Gunn, James E.

    1991-01-01

    Moderate-resolution spectroscopy of an unusual late-type faint emission-line star, PC 0025 + 0047, is reported. A very strong (greater than 250 A equivalent width) an H-alpha emission line was detected by the present automated line search algorithm. The spectrum was found to have two unresolved emission lines (H-alpha and H-beta) near zero velocity, superposed on the absorption spectrum of a very red M dwarf which has strong K I, and relatively weak bands of TiO. From the weakness of the subordinate lines of Na I (8192 A) and other spectral features, it is inferred that it is definitely a cooler, and probably fainter, analog of LHS 2924. The strength of the emission lines indicates that PC 0025 + 0447 is very young and may be a fading predecessor brown drawf at an estimated M(bol) approaching 14m at a distance of about 60 pc.

  10. Probing Local Environments by Time-Resolved Stimulated Emission Spectroscopy

    Directory of Open Access Journals (Sweden)

    Ana Rei

    2012-01-01

    Full Text Available Time-resolved stimulated emission spectroscopy was employed to probe the local environment of DASPMI (4-(4-(dimethylaminostyryl-N-methyl-pyridinium iodide in binary solvents of different viscosity and in a sol-gel matrix. DASPMI is one of the molecules of choice to probe local environments, and the dependence of its fluorescence emission decay on viscosity has been previously used for this purpose in biological samples, solid matrices as well as in solution. The results presented in this paper show that time-resolved stimulated emission of DASPMI is a suitable means to probe the viscosity of local environments. Having the advantage of a higher time resolution, stimulated emission can provide information that is complementary to that obtained from fluorescence decay measurements, making it feasible to probe systems with lower viscosity.

  11. Modelling of new generation plasma optical devices

    Directory of Open Access Journals (Sweden)

    Litovko Irina V.

    2016-06-01

    Full Text Available The paper presents new generation plasma optical devices based on the electrostatic plasma lens configuration that opens a novel attractive possibility for effective high-tech practical applications. Original approaches to use of plasma accelerators with closed electron drift and open walls for the creation of a cost-effective low-maintenance plasma lens with positive space charge and possible application for low-cost, low-energy rocket engine are described. The preliminary experimental, theoretical and simulation results are presented. It is noted that the presented plasma devices are attractive for many different applications in the state-of-the-art vacuum-plasma processing.

  12. Emission Line Imaging and Spectroscopy of Distant Galaxies

    DEFF Research Database (Denmark)

    Zabl, Johannes Florian

    determinations even at lowest masses and highest redshifts. Finally, emission lines can be used in the first place to select large samples of galaxies at well defined redshifts through narrowband (NB) surveys, as the presence of a line in the NB filter raises the flux compared to that expected from the continuum...... for the gas surrounding a galaxy. Around some objects the extended Ly αemission is so strong that it can be detected for individual objects. In this thesis extremely deep VLT/XSHOOTER rest-frame far-UV spectroscopy is presented for Himiko, a gigantic Ly α emitter at redshift z = 6.6 or a time when...

  13. Supplemental Report: Application of Emission Spectroscopy to Monitoring Technetium

    Energy Technology Data Exchange (ETDEWEB)

    Spencer, W.A.

    2000-07-27

    This report provides supplemental information to an earlier report BNF-98-003-0199, ''Evaluation of Emission Spectroscopy for the On-Line Analysis of Technetium''. In this report data is included from real Hanford samples as well as for solutions spiked with technetium. This supplemental work confirms the ability of ICP-ES to monitor technetium as it breaks through an ion exchange process.

  14. Current Problems in X-Ray Emission Spectroscopy

    Science.gov (United States)

    Goldstein, Joseph I.; Williams, David B.; Lyman, Charles E.

    1989-01-01

    Various problems that limit X-ray analysis in the analytical electron microscope are reviewed. Major emphasis is given to the trade-off between minimum mass fraction and spatial resolution. New developments such as high-brightness electron guns, new X-ray spectrometers and clean high-vacuum analysis conditions will lead to major improvements in the accuracy and detectability limits of X-ray emission spectroscopy.

  15. Determinação dos teores de minerais em sucos de frutas por espectrometria de emissão óptica em plasma indutivamente acoplado (ICP-OES Minerals determination in juices by inductively coupled plasma optical emission spectrometry

    Directory of Open Access Journals (Sweden)

    Marcelo Antônio MORGANO

    1999-12-01

    Full Text Available Dois métodos de preparação de amostra para determinação de minerais em suco de uva foram comparados: extração com ácido clorídrico a frio com agitação e digestão em sistema fechado, sob pressão, empregando-se energia de microondas. As concentrações dos minerais foram obtidas empregando-se a técnica de Espectrometria de Emissão Óptica em Plasma Indutivamente Acoplado (ICP-OES. Os teores dos minerais Ca, P, Na, K, Mg, Zn, Fe, Mn e Cu não diferiram significativamente ao nível de 5% (Teste F para as duas metodologias empregadas. A precisão e exatidão dos métodos foi avaliada usando o suco de uva. A metodologia de extração com ácido clorídrico foi empregada para a determinação dos teores de minerais em sucos processados de abacaxi, acerola, caju, goiaba, manga, maracujá e uva. Para facilitar a interpretação dos teores dos minerais encontrados, foram utilizadas as técnicas de Análise por Componentes Principais (PCA e Análise Hierárquica por Agrupamento (HCA.Two sample preparation methods for the determination of minerals from grape juice were investigated for the purpose of methodological evaluation: using hydrochloric acid by shaking, and digestion in closed system, under pressure, using microwave power. The concentrations of minerals were evaluated by the technique of Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES. The minerals contents of Ca, P, Na, K, Mg, Zn, Fe, Mn, and Cu did not differ significantly at the level of 5% (it Tests F for both methodologies used. The precision and accuracy of both methodologies were evaluated using grape juice. The extraction methodology with hydrochloric acid was used for the determination of mineral amounts in processed juices from pineapple, acerola, cashew, guava, mango, passion fruit and grape. To enhance the interpretation of the amounts of minerals, from a nutritional point of view, techniques of Principal Components Analysis (PCA and Hierarchic Cluster

  16. Absorption/emission spectroscopy and applications using shock tubes

    Science.gov (United States)

    Sulzmann, K. G. P.

    1988-09-01

    A historical overview is presented about the important contributions made by Penner, his co-workers, and his students to the application of shock-tube techniques for quantitative emission and absorption spectroscopy and its applications to chemical kinetics studies in high-temperature gases. The discussions address critical aspects related to valid determinations of quantitative spectroscopic data and chemical rate parameters and stress the requirements for uniformly heated gas samples, temperature determinations, gas-mixture preparations, selection of useful spectral intervals, verification of LTE conditions, time resolutions for concentration histories, uniqueness of kinetic measurements, as well as accuracies and reproducibilities of measurement results.The potential of absorption spectroscopy by molecule and/or radical resonance radiation and by laser transmission techniques is highlighted for kinetic studies in mixtures with very small reactant concentrations.Besides the work by the honoree and his school, the references include books, monographs and key articles related to the subjects discussed.

  17. Fluorescence-excitation and Emission Spectroscopy on Single FMO Complexes.

    Science.gov (United States)

    Löhner, Alexander; Ashraf, Khuram; Cogdell, Richard J; Köhler, Jürgen

    2016-08-22

    In green-sulfur bacteria sunlight is absorbed by antenna structures termed chlorosomes, and transferred to the RC via the Fenna-Matthews-Olson (FMO) complex. FMO consists of three monomers arranged in C3 symmetry where each monomer accommodates eight Bacteriochlorophyll a (BChl a) molecules. It was the first pigment-protein complex for which the structure has been determined with high resolution and since then this complex has been the subject of numerous studies both experimentally and theoretically. Here we report about fluorescence-excitation spectroscopy as well as emission spectroscopy from individual FMO complexes at low temperatures. The individual FMO complexes are subjected to very fast spectral fluctuations smearing out any possible different information from the ensemble data that were recorded under the same experimental conditions. In other words, on the time scales that are experimentally accessible by single-molecule techniques, the FMO complex exhibits ergodic behaviour.

  18. Hard X-ray emission spectroscopy with pink beam

    Energy Technology Data Exchange (ETDEWEB)

    Kvashnina, Kristina O.; Rossberg, Andre; Exner, Joerg; Scheinost, Andreas C. [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Molecular Structures

    2017-06-01

    Valence-band X-ray emission spectroscopy (XES) with a ''pink beam'', i.e. a beam with large energy bandwidth produced by a double-multilayer monochromator, is introduced here to overcome the weak count rate of monochromatic beams produced by conventional double-crystal monochromators. Our results demonstrate that - in spite of the large bandwidth in the order of 100 eV - the high spectral resolution of the Johann-type spectrometer is maintained, while the two orders of magnitude higher flux greatly reduces the required counting time. The short working distance Johann-type X-ray emission spectrometer and multilayer monochromator is available at ROBL.

  19. Photon emission spectroscopy of ion-atom collisions

    Energy Technology Data Exchange (ETDEWEB)

    Nystroem, B.

    1995-10-01

    Emission cross sections for the 1snp{sup 1}P{sub 1}-levels have been measured by photon emission spectroscopy for the collision systems He{sup +} + He at 10 keV and He{sup 2+} + He at 10-35 keV. Photon spectra of Krypton (Kr VIII) and Xenon (Xe V - IX) have also been obtained using 10q keV beams of Kr{sup q+} (q=7-9) and Xe{sup q+} (q=5-9) colliding with Helium and Argon. The Lifetimes of 3p{sup 2}P-levels in Na-like Nb are reported together with lifetime for the 3s3p{sup 3}P{sub 1}-level in Mg-like Ni, Kr, Y, Zr and Nb where this level has an intercombination transition to the ground state. 45 refs, 20 figs.

  20. Emission Spectroscopy of the Super-Earth 55 Cnc e

    Science.gov (United States)

    Dragomir, Diana; Bean, Jacob; Kreidberg, Laura; Stevenson, Kevin B.; Line, Michael R.

    2017-01-01

    Recent surveys have revealed an extraordinary and unexplained diversity of low-mass exoplanets. The main frontier for constraining the nature and origins of these planets is atmospheric characterization to reveal their detailed physical properties. Previous spectroscopic observations of small exoplanets have been focused on transmission measurements, but these studies are often limited by clouds. We are turning small exoplanet characterization in a new direction with multi-wavelength observations (Warm Spitzer and HST WFC3) of the dayside of 55 Cnc e, a quintessential super-Earth in a tight orbit and transiting a nearby star. We will present the first dayside emission spectrum of a super-Earth, which we use to distinguish between different atmospheric compositions and constrain the vertical temperature structure of the atmosphere. Our results for 55 Cnc e will guide JWST emission spectroscopy of a much larger sample of small close-in transiting exoplanets.

  1. Emission Line Imaging and Spectroscopy of Distant Galaxies

    DEFF Research Database (Denmark)

    Zabl, Johannes Florian

    determinations even at lowest masses and highest redshifts. Finally, emission lines can be used in the first place to select large samples of galaxies at well defined redshifts through narrowband (NB) surveys, as the presence of a line in the NB filter raises the flux compared to that expected from the continuum...... applied a novel NB measurement method to a sample of UltraVISTA NB118 H α emitters, and demonstrate that this technique allows to recover more accurate fluxes. Additionally, the method allows to determine more accurate redshifts. Contemporary NB surveys have a strong focus on searches for Ly α emitters...... for the gas surrounding a galaxy. Around some objects the extended Ly αemission is so strong that it can be detected for individual objects. In this thesis extremely deep VLT/XSHOOTER rest-frame far-UV spectroscopy is presented for Himiko, a gigantic Ly α emitter at redshift z = 6.6 or a time when...

  2. Microwaves spark emission spectroscopy for the analysis of cations: A simple form of atomic emission spectroscopy

    Institute of Scientific and Technical Information of China (English)

    Zahid Hussain; Khalid Mohammed Khan; Khadim Hussain; Sadam Hussain; Shahnaz Perveen

    2011-01-01

    A novel method for the cation analysis was investigated. The analysis is based on the sparking of the salts of metals in a microwave oven after placing in a graphite cell. The graphite cell absorbs microwaves and produces high temperature which converts the salt into light emitting species. The colour of light was found to dependent on the nature of cation, however, the intensity of the emitted light was found to be depending upon the form and shape of the graphite assembly in addition to the concentration of the salt. This communication presents explanation for all these observations and for the systematic and quantitative analysis using microwave spark emission technique.

  3. Detection of Bioaerosols Using Single Particle Thermal Emission Spectroscopy (First-year Report)

    Science.gov (United States)

    2012-02-01

    Detection of Bioaerosols using Single Particle Thermal Emission Spectroscopy (First-year Report) by Dr. Kristan P. Gurton, Melvin Felton, and...Research Laboratory Adelphi, MD 20783-1197 ARL-TR-5934 February 2012 Detection of Bioaerosols using Single Particle Thermal Emission...October 2011 4. TITLE AND SUBTITLE Detection of Bioaerosols using Single Particle Thermal Emission Spectroscopy (First-year Report) 5a. CONTRACT

  4. BATMAN beam properties characterization by the beam emission spectroscopy diagnostic

    Science.gov (United States)

    Bonomo, F.; Ruf, B.; Barbisan, M.; Cristofaro, S.; Schiesko, L.; Fantz, U.; Franzen, P.; Pasqualotto, R.; Riedl, R.; Serianni, G.; Wünderlich, D.

    2015-04-01

    The ITER neutral beam heating systems are based on the production and acceleration of negative ions (H/D) up to 1 MV. The requirements for the beam properties are strict: a low core beam divergence (BATMAN (BAvarian Test MAchine for Negative ions) allows for deepening the knowledge of the determination of the beam properties. One of the diagnostics routinely used to this purpose is the Beam Emission Spectroscopy (BES): the Hα light emitted in the beam is detected and the corresponding spectra are evaluated to estimate the beam divergence and the stripping losses. The BES number of lines of sight in BATMAN has been recently increased: five horizontal lines of sight providing a vertical profile of the beam permit to characterize the negative ion beam properties in relation to the source parameters. Different methods of Hα spectra analysis are here taken into account and compared for the estimation of the beam divergence and the amount of stripping. In particular, to thoroughly study the effect of the space charge compensation on the beam divergence, an additional hydrogen injection line has been added in the tank, which allows for setting different background pressure values (one order of magnitude, from about 0.04 Pa up to the source pressure) in the beam drift region.

  5. X-ray Emission Spectroscopy of Biomimetic Mn Coordination Complexes.

    Science.gov (United States)

    Jensen, Scott C; Davis, Katherine M; Sullivan, Brendan; Hartzler, Daniel A; Seidler, Gerald T; Casa, Diego M; Kasman, Elina; Colmer, Hannah E; Massie, Allyssa A; Jackson, Timothy A; Pushkar, Yulia

    2017-06-15

    Understanding the function of Mn ions in biological and chemical redox catalysis requires precise knowledge of their electronic structure. X-ray emission spectroscopy (XES) is an emerging technique with a growing application to biological and biomimetic systems. Here, we report an improved, cost-effective spectrometer used to analyze two biomimetic coordination compounds, [Mn(IV)(OH)2(Me2EBC)](2+) and [Mn(IV)(O)(OH)(Me2EBC)](+), the second of which contains a key Mn(IV)═O structural fragment. Despite having the same formal oxidation state (Mn(IV)) and tetradentate ligands, XES spectra from these two compounds demonstrate different electronic structures. Experimental measurements and DFT calculations yield different localized spin densities for the two complexes resulting from Mn(IV)-OH conversion to Mn(IV)═O. The relevance of the observed spectroscopic changes is discussed for applications in analyzing complex biological systems such as photosystem II. A model of the S3 intermediate state of photosystem II containing a Mn(IV)═O fragment is compared to recent time-resolved X-ray diffraction data of the same state.

  6. Avalanche photodiode based detector for beam emission spectroscopy.

    Science.gov (United States)

    Dunai, D; Zoletnik, S; Sárközi, J; Field, A R

    2010-10-01

    An avalanche photodiode based (APD) detector for the visible wavelength range was developed for low light level, high frequency beam emission spectroscopy (BES) experiments in fusion plasmas. This solid state detector has higher quantum efficiency than photomultiplier tubes, and unlike normal photodiodes, it has internal gain. This paper describes the developed detector as well as the noise model of the electronic circuit. By understanding the noise sources and the amplification process, the optimal amplifier and APD reverse voltage setting can be determined, where the signal-to-noise ratio is the highest for a given photon flux. The calculations are compared to the absolute calibration results of the implemented circuit. It was found that for a certain photon flux range, relevant for BES measurements (≈10(8)-10(10) photons/s), the new detector is superior to both photomultipliers and photodiodes, although it does not require cryogenic cooling of any component. The position of this photon flux window sensitively depends on the parameters of the actual experimental implementation (desired bandwidth, detector size, etc.) Several detector units based on these developments have been built and installed in various tokamaks. Some illustrative results are presented from the 8-channel trial BES system installed at Mega-Ampere Spherical Tokamak (MAST) and the 16-channel BES system installed at the Torus Experiment for Technology Oriented Research (TEXTOR).

  7. Optical emission spectroscopy study on deposition process of microcrystalline silicon

    Institute of Scientific and Technical Information of China (English)

    Wu Zhi-Meng; Lei Qing-Song; Geng Xin-Hua; Zhao Ying; Sun Jian; Xi Jian-Ping

    2006-01-01

    This paper reports that the optical emission spectroscopy (OES) is used to monitor the plasma during the deposition process of hydrogenated microcrystalline silicon films in a very high frequency plasma enhanced chemical vapour deposition system. The OES intensities (SiH*, H*α and H*β) are investigated by varying the deposition parameters. The result shows that the discharge power, silane concentrations and substrate temperature affect the OES intensities. When the discharge power at silane concentration of 4% increases, the OES intensities increase first and then are constant, the intensities increase with the discharge power monotonously at silane concentration of 6%. The SiH* intensity increases with silane concentration, while the intensities of H*α and H*β increase first and then decrease. When the substrate temperature increases, the SiH* intensity decreases and the intensities of H*α and H*β are constant. The correlation between the intensity ratio of IH*α/ISiH* and the crystalline volume fraction (Xc) of films is confirmed.

  8. Optical emission spectroscopy of argon and hydrogen-containing plasmas

    Science.gov (United States)

    Siepa, Sarah; Danko, Stephan; Tsankov, Tsanko V.; Mussenbrock, Thomas; Czarnetzki, Uwe

    2015-09-01

    Optical emission spectroscopy (OES) on neutral argon is applied to investigate argon, hydrogen and hydrogen-silane plasmas. The spectra are analyzed using an extensive collisional-radiative model (CRM), from which the electron density and the electron temperature (or mean energy) can be calculated. The CRM also yields insight into the importance of different excited species and kinetic processes. The OES measurements are performed on pure argon plasmas at intermediate pressure. Besides, hydrogen and hydrogen-silane plasmas are investigated using argon as a trace gas. Especially for the gas mixture discharges, CRMs for low and high pressure differ substantially. The commonly used line-ratio technique is found to lose its sensitivity for gas mixture discharges at higher pressure. A solution using absolutely calibrated line intensities is proposed. The effect of radiation trapping and the shape of the electron energy distribution function on the results are discussed in detail, as they have been found to significantly influence the results. This work was supported by the Ruhr University Research School PLUS, funded by Germany's Excellence Initiative [DFG GSC 98/3].

  9. High-Resolution X-ray Emission and X-ray Absorption Spectroscopy

    NARCIS (Netherlands)

    Groot, F.M.F. de

    2000-01-01

    In this review, high-resolution X-ray emission and X-ray absorption spectroscopy will be discussed. The focus is on the 3d transition-metal systems. To understand high-resolution X-ray emission and reso-nant X-ray emission, it is first necessary to spend some time discussing the X-ray absorption

  10. BATMAN beam properties characterization by the beam emission spectroscopy diagnostic

    Energy Technology Data Exchange (ETDEWEB)

    Bonomo, F., E-mail: federica.bonomo@igi.cnr.it [Consorzio RFX (CNR, ENEA, INFN, Università di Padova, Acciaierie Venete SpA), Corso Stati Uniti 4, 35127 Padova (Italy); Istituto Gas Ionizzati - CNR, Corso Stati Uniti 4, 35127 Padova (Italy); Ruf, B.; Schiesko, L.; Fantz, U.; Franzen, P.; Riedl, R.; Wünderlich, D. [Max-Planck-Institut für Plasmaphysik, Boltzmannstr. 2, 85748 Garching (Germany); Barbisan, M.; Pasqualotto, R.; Serianni, G. [Consorzio RFX (CNR, ENEA, INFN, Università di Padova, Acciaierie Venete SpA), Corso Stati Uniti 4, 35127 Padova (Italy); Cristofaro, S. [Universitá degli Studi di Padova, Via 8 Febbraio 2, 35122 Padova (Italy)

    2015-04-08

    The ITER neutral beam heating systems are based on the production and acceleration of negative ions (H/D) up to 1 MV. The requirements for the beam properties are strict: a low core beam divergence (< 0.4 °) together with a low source pressure (≤ 0.3 Pa) would permit to reduce the ion losses along the beamline, keeping the stripping particle losses below 30%. However, the attainment of such beam properties is not straightforward. At IPP, the negative ion source testbed BATMAN (BAvarian Test MAchine for Negative ions) allows for deepening the knowledge of the determination of the beam properties. One of the diagnostics routinely used to this purpose is the Beam Emission Spectroscopy (BES): the H{sub α} light emitted in the beam is detected and the corresponding spectra are evaluated to estimate the beam divergence and the stripping losses. The BES number of lines of sight in BATMAN has been recently increased: five horizontal lines of sight providing a vertical profile of the beam permit to characterize the negative ion beam properties in relation to the source parameters. Different methods of H{sub α} spectra analysis are here taken into account and compared for the estimation of the beam divergence and the amount of stripping. In particular, to thoroughly study the effect of the space charge compensation on the beam divergence, an additional hydrogen injection line has been added in the tank, which allows for setting different background pressure values (one order of magnitude, from about 0.04 Pa up to the source pressure) in the beam drift region.

  11. Optical emission spectroscopy of the Linac4 and superconducting proton Linac plasma generators

    Energy Technology Data Exchange (ETDEWEB)

    Lettry, J.; Kronberger, M.; Mahner, E.; Schmitzer, C.; Sanchez, J.; Scrivens, R.; Midttun, O.; O' Neil, M.; Pereira, H.; Paoluzzi, M. [European Organization for Nuclear Research, CERN, 1211 Geneva 23 (Switzerland); Fantz, U.; Wuenderlich, D. [Max-Planck-Institut fuer Plasmaphysik, IPP, 85748 Garching (Germany); Kalvas, T.; Koivisto, H.; Komppula, J.; Myllyperkioe, P.; Tarvainen, O. [Department of Physics, University of Jyvaeskylae, 40500 Jyvaeskylae (Finland)

    2012-02-15

    CERN's superconducting proton Linac (SPL) study investigates a 50 Hz high-energy, high-power Linac for H{sup -} ions. The SPL plasma generator is an evolution of the DESY ion source plasma generator currently operated at CERN's Linac4 test stand. The plasma generator is a step towards a particle source for the SPL, it is designed to handle 100 kW peak RF-power at a 6% duty factor. While the acquisition of an integrated hydrogen plasma optical spectrum is straightforward, the measurement of a time-resolved spectrum requires dedicated amplification schemes. The experimental setup for visible light based on photomultipliers and narrow bandwidth filters and the UV spectrometer setup are described. The H{sub {alpha}}, H{sub {beta}}, and H{sub {gamma}} Balmer line intensities, the Lyman band and alpha transition were measured. A parametric study of the optical emission from the Linac4 ion source and the SPL plasma generator as a function of RF-power and gas pressure is presented. The potential of optical emission spectrometry coupled to RF-power coupling measurements for on-line monitoring of short RF heated hydrogen plasma pulses is discussed.

  12. Analysis of trace elements in food fortificants with inductively coupled plasma optical emission spectrometry%电感耦合等离子体原子发射光谱分析食品营养强化剂中的痕量元素

    Institute of Scientific and Technical Information of China (English)

    段建坤; 曾爱民; 杨永; 朱有涛; 唐立平; 沈丽

    2011-01-01

    A simple and fast method was developed for the determination of Ca, K, Na, Fe, Zn, Mn, Pb and As in food fortificants by inductively coupled plasma optical emission spectrometry (ICP-OES). The effect of the sample matrix was studied and the results showed that there was little matrix effect existing if the concentration of the organic food fortificants and inorganic metal ion in the sample solution were no more than 20 and 2 g/L, respectively. Three methods for sample pretreatment were investigated and compared. External standard and matrix matching methods were used for quantification of the analytes in the samples. It is found than the former showed better analytical performances. The proposed method was applied for the analysis of six food fortificants with satisfied recoveries.%以电感耦合等离子体发射光谱(ICP—OES)作为检测手段分析了营养强化剂中的钙、钾、钠、铁、锌、锰、铅和砷等元素。研究了样品基体对于分析过程的影响,实验结果表明,有机强化剂浓度不超过20g/L,无机强化剂中的无机金属元素含量不超过2g/L时,可以认为基体没有影响。考察了不同的样品处理方式的优缺点。比较了校正曲线法(外标法)和基体匹配法两种定量分析方法,发现前者的分析性能更为优越。分析了6种强化剂中的钙、钾、钠、铁、锌、锰、铅和砷,加标回收结果满意。

  13. Transmittance, Reflectance, and Emission Spectroscopy of Meteorites from the UV to the IR Spectral Range

    Science.gov (United States)

    Maturilli, A.; Helbert, J.; Koulen, J. M.; Ferrari, S.; Martellato, E.

    2016-08-01

    Transmittance, reflectance, and emissivity Spectra of six meteorites have been collected at the Planetary Spectroscopy Laboratory (PSL) of DLR in Berlin in the whole spectral range from the UV to the IR.

  14. MEASUREMENT OF AMMONIA EMISSIONS FROM MECHANICALLY VENTILATED POULTRY HOUSES USING MULTIPATH TUNABLE DIODE LASER SPECTROSCOPY

    Science.gov (United States)

    Ammonia emissions from mechanically ventilated poultry operations are an important environmental concern. Open Path Tunable Diode Laser Absorption Spectroscopy has emerged as a robust real-time method for gas phase measurement of ammonia concentrations in agricultural settings. ...

  15. Analysis of quantum semiconductor heterostructures by ballistic electron emission spectroscopy

    Science.gov (United States)

    Guthrie, Daniel K.

    1998-09-01

    The microelectronics industry is diligently working to achieve the goal of gigascale integration (GSI) by early in the 21st century. For the past twenty-five years, progress toward this goal has been made by continually scaling down device technology. Unfortunately, this trend cannot continue to the point of producing arbitrarily small device sizes. One possible solution to this problem that is currently under intensive study is the relatively new area of quantum devices. Quantum devices represent a new class of microelectronic devices that operate by utilizing the wave-like nature (reflection, refraction, and confinement) of electrons together with the laws of quantum mechanics to construct useful devices. One difficulty associated with these structures is the absence of measurement techniques that can fully characterize carrier transport in such devices. This thesis addresses this need by focusing on the study of carrier transport in quantum semiconductor heterostructures using a relatively new and versatile measurement technique known as ballistic electron emission spectroscopy (BEES). To achieve this goal, a systematic approach that encompasses a set of progressively more complex structures is utilized. First, the simplest BEES structure possible, the metal/semiconductor interface, is thoroughly investigated in order to provide a foundation for measurements on more the complex structures. By modifying the semiclassical model commonly used to describe the experimental BEES spectrum, a very complete and accurate description of the basic structure has been achieved. Next, a very simple semiconductor heterostructure, a Ga1-xAlxAs single-barrier structure, was measured and analyzed. Low-temperature measurements on this structure were used to investigate the band structure and electron-wave interference effects in the Ga1-xAlxAs single barrier structure. These measurements are extended to a simple quantum device by designing, measuring, and analyzing a set of

  16. Absorption and emission spectroscopy in natural and synthetic corundum

    Science.gov (United States)

    Spinolo, G.; Palanza, V.; Ledonne, A.; Paleari, A.

    2009-04-01

    In the frame of an extensive project on the optical characterization of the many varieties of corundum (see:www.gemdata.mater.unimib.it ) we reconsidered the current interpretation of the absorption spectra with particular attention to the bands attributed to the IVCT mechanism Fe2+→ Fe3+ and Fe2+→Ti4+. A detailed study was devoted to natural metamorphic and Verneuil synthetic pale blue sapphires . In that paper (I.Fontana et al 2008) we gave experimental evidence that the band at 17500 cm-1 often attributed to Fe2+→Ti4+ IVCT transitions is in reality due to the 4T2 crystal field transition of Cr3+ partially overlapped by the 2E of Ti3+. The results of radio and photoluminescence excitation experiments obtained there, led us to propose that the color of these sapphires is mainly due to Cr in its two valence states ; Ti 3+ and Fe3+ have a minor role. After those encouraging results, we decided to apply the same approach to the study of deep blue and yellow sapphires of magmatic origin. Evaluation of impurity ion concentration by EDXRF revealed that in all these samples the concentration of Fe is quite high (around 1%) while Cr and Ti are barely detectable. Characteristic of the absorption spectra of deep blue samples is the dominant presence of the 5E spin allowed transition of Fe2+; Fe3+ has a minor role due to the fact that all d5 transitions are spin forbidden and ,consequently, very weak. In yellow sapphires Fe is totally in its 3+ valence state. In these cases, the color from yellow to blue, sometimes even within the same sample, depends. on oxidizing or reducing growth conditions. Even if the concentrations of Cr and Ti are very low, their characteristic emissions are the only ones observable down to 10000 cm-1 in radio and photoluminescence spectra. This piece of evidence suggested us to propose for the absorption bands present in the 14000 to 21000 cm-1 range, often attributed to IVCT, the same attribution given to the analogous bands in metamorphic

  17. Multiple stimulated emission fluorescence photoacoustic sensing and spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Li, Gaoming [School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore 639798 (Singapore); Key Laboratory of OptoElectronic Science and Technology for Medicine, Ministry of Education, Fujian Normal University, Fuzhou 350007 (China); Gao, Fei; Feng, Xiaohua; Zheng, Yuanjin, E-mail: yjzheng@ntu.edu.sg [School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore 639798 (Singapore); Qiu, Yishen [Key Laboratory of OptoElectronic Science and Technology for Medicine, Ministry of Education, Fujian Normal University, Fuzhou 350007 (China)

    2016-07-04

    Multiple stimulated emission fluorescence photoacoustic (MSEF-PA) phenomenon is demonstrated in this letter. Under simultaneous illumination of pumping light and stimulated emission light, the fluorescence emission process is speeded up by the stimulated emission effect. This leads to nonlinear enhancement of photoacoustic signal while the quantity of absorbed photons is more than that of fluorescent molecules illuminated by pumping light. The electronic states' specificity of fluorescent molecular can also be labelled by the MSEF-PA signals, which can potentially be used to obtain fluorescence excitation spectrum in deep scattering tissue with nonlinearly enhanced photoacoustic detection. In this preliminary study, the fluorescence excitation spectrum is reconstructed by MSEF-PA signals through sweeping the wavelength of exciting light, which confirms the theoretical derivation well.

  18. Thermal Emissivity-Based Chemical Spectroscopy through Evanescent Tunneling.

    Science.gov (United States)

    Poole, Zsolt L; Ohodnicki, Paul R

    2016-04-01

    A new spectroscopic technique is presented, with which environmentalchemistry-induced thermal emissivity changes of thin films are extracted with high isolation through evanescent tunneling. With this method the hydrogen-induced emissivity changes of films of TiO2 , Pd-TiO2 , and Au-TiO2 , with properties of high conductivity, hydrogen chemisorption, and plasmonic activity, are characterized in the UV-vis and NIR wavelength ranges, at 1073 K.

  19. Transmission And Emission Spectroscopy Of Exoplanetary Atmospheres From The Ground

    Science.gov (United States)

    Waldmann, Ingo

    2010-01-01

    It has been shown in recent years with great success that spectroscopy of exoplanetary atmospheres is feasible using space based observatories such as the HST and Spitzer. However, with the end of the Spitzer cold-phase, space based observations in the near to mid infra-red are limited, which will remain true until the the onset of the JWST. The importance of developing methods of ground based spectroscopic analysis of known hot Jupiters is therefore apparent. In the past, various groups have attempted exoplanetary spectroscopy using ground based facilities and various techniques. Here I like to present some preliminary results on a new attempt of the ground based efforts and discuss the feasibility of ground-based spectroscopy of exoplanetary atmospheres. This project is under the supervision of Giovanna Tinetti (University College London) and in collaboration with J. P. Beaulieu (Institut d'Astrophysique de Paris), Mark Swain and Pieter Deroo (Jet Propulsion Laboratory, Caltech).

  20. Determination of Nb and Ta in Nb-Ta Ore by Inductively Coupled Plasma-Optical Emission Spectrometry with a Combined Microwave Digestion Hydrofluoric Acid-resistant System%微波消解-耐氢氟酸系统电感耦合等离子体发射光谱法测定铌钽矿中的铌和钽

    Institute of Scientific and Technical Information of China (English)

    马生凤; 温宏利; 李冰; 王蕾; 朱云

    2016-01-01

    Niobium and tantalum in hydrofluoric acid can form a stable solution,and thus the Nb and Ta content of Nb-Ta ore can be determined accurately by Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES) with a hydrofluoric acid resistant system.The determination method described in this paper for Nb and Ta in Nb-Ta ore,uses the microwave digestion mode of modular small tank and multiple digestion tank assembly (70 tank /group),and hydrofluoric acid resistant system of ICP-OES.This method shortens the dissolution time from 48 h to 1 h.By using a hydrofluoric acid medium the hydrolysis of high-level Nb and Ta in low acid concentration media is avoided.The detection limits of this method are 5.58 μg/g for Nb and 5.87 μg/g for Ta.The result of Nb-Ta concentrate with 19% Nb2 O5 and 27% Ta2 O5 is consistent with that acquired by the alkali fusion method and can be used to determine both high-grade and low-grade Nb-Ta ore with 42 μg/g -19% of Nb2 O5 and 86 μg/g -27%of Ta2 O5 .The main advantage of this method is to accurately determine Nb and Ta in high-grade Nb-Ta ore.%铌、钽在氢氟酸介质中能够形成稳定的溶液,使用耐氢氟酸进样系统的电感耦合等离子体发射光谱(ICP -OES)有利于提高分析的准确性。本文采用模块化的小罐型、多罐体组合(70罐/组)酸溶罐体的微波消解溶样模式,结合 ICP -OES 仪器的耐氢氟酸进样系统,建立了测定铌钽矿中铌、钽的分析方法。本方法加快了酸溶的溶样速度,溶样时间从原来的48 h 减少至1 h,且在氢氟酸介质中测定避免了高含量铌、钽在低酸度介质中容易水解的影响。方法检出限为铌5.58μg/g,钽5.87μg/g。本方法应用于测定铌钽精矿(19%Nb2 O5,27%Ta2 O5)的分析结果与碱熔方法一致,能够测定 Nb2 O5含量在42μg/g ~19%和 Ta2 O5含量在86μg/g ~27%高低品位的铌钽矿,尤其对于铌、钽在百分含量以上的铌钽矿具有优势。

  1. High-Resolution X-ray Emission and X-ray Absorption Spectroscopy

    OpenAIRE

    de Groot, F. M. F.

    2001-01-01

    In this review, high-resolution X-ray emission and X-ray absorption spectroscopy will be discussed. The focus is on the 3d transition-metal systems. To understand high-resolution X-ray emission and reso-nant X-ray emission, it is first necessary to spend some time discussing the X-ray absorption process. Section II discusses 1s X-ray absorption, i.e., the K edges, and section III deals with 2p X-ray absorption, the L edges. X-ray emission is discussed in, respectively, the L edges. X-ray emis...

  2. Non-coincident multi-wavelength emission absorption spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Baumann, L.E.

    1995-02-01

    An analysis is presented of the effect of noncoincident sampling on the measurement of atomic number density and temperature by multiwavelength emission absorption. The assumption is made that the two signals, emission and transmitted lamp, are time resolved but not coincident. The analysis demonstrates the validity of averages of such measurements despite fluctuations in temperature and optical depth. At potassium-seeded MHD conditions, the fluctuations introduce additional uncertainty into measurements of potassium atom number density and temperature but do not significantly bias the average results. Experimental measurements in the CFFF aerodynamic duct with coincident and noncoincident sampling support the analysis.

  3. Detection of Bioaerosols using Single Particle Thermal Emission Spectroscopy

    Science.gov (United States)

    2013-03-01

    droplets was accomplished by using a peristaltic pump to inject a set flow-rate of liquid mineral oil into a heated hypodermic needle . Heated mineral...heated to temperatures in excess of a 100 °C. Prevailing theory suggests a strong link between thermal emission and absorption spectra for bulk...iv 1. Background 1 2. Theory 1 3. Experiment 5 4. Results 13 5. Conclusion 16 6. References 18 List of Symbols, Abbreviations, and Acronyms 20

  4. Real-time tissue differentiation based on optical emission spectroscopy for guided electrosurgical tumor resection

    OpenAIRE

    Spether, Dominik; Scharpf, Marcus; Hennenlotter, Jörg; Schwentner, Christian; Neugebauer, Alexander; Nüßle, Daniela; Fischer, Klaus; Zappe, Hans; Stenzl, Arnulf; Fend, Falko; Seifert, Andreas; Enderle, Markus

    2015-01-01

    Complete surgical removal of cancer tissue with effective preservation of healthy tissue is one of the most important challenges in modern oncology. We present a method for real-time, in situ differentiation of tissue based on optical emission spectroscopy (OES) performed during electrosurgery not requiring any biomarkers, additional light sources or other excitation processes. The analysis of the optical emission spectra, enables the differentiation of healthy and tumorous tissue. By using m...

  5. Emission Spectroscopy of the Interior of Optically Dense Post-Detonation Fireballs

    Science.gov (United States)

    2013-03-01

    TP-2013-011 Emission Spectroscopy of the Interior of Optically Dense Post-Detonation Fireballs Distribution A: Approved for public release...Detonation Fireballs 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 62102F 6. AUTHOR(S) W.K. Lewis1, C.G. Rumchik2, M.J...detonation fireballs that form as under- oxidized detonation products burn in the surrounding air are optically dense and the corresponding emission

  6. A GAS TEMPERATURE PROFILE BY INFRARED EMISSION-ABSORPTION SPECTROSCOPY

    Science.gov (United States)

    Buchele, D. R.

    1994-01-01

    This computer program calculates the temperature profile of a flame or hot gas. Emphasis is on profiles found in jet engine or rocket engine exhaust streams containing water vapor or carbon dioxide as radiating gases. The temperature profile is assumed to be axisymmetric with a functional form controlled by two variable parameters. The parameters are calculated using measurements of gas radiation at two wavelengths in the infrared spectrum. Infrared emission and absorption measurements at two or more wavelengths provide a method of determining a gas temperature profile along a path through the gas by using a radiation source and receiver located outside the gas stream being measured. This permits simplified spectral scanning of a jet or rocket engine exhaust stream with the instrumentation outside the exhaust gas stream. This program provides an iterative-cyclic computation in which an initial assumed temperature profile is altered in shape until the computed emission and absorption agree, within specified limits, with the actual instrument measurements of emission and absorption. Temperature determination by experimental measurements of emission and absorption at two or more wavelengths is also provided by this program. Additionally, the program provides a technique for selecting the wavelengths to be used for determining the temperature profiles prior to the beginning of the experiment. By using this program feature, the experimenter has a higher probability of selecting wavelengths which will result in accurate temperature profile measurements. This program provides the user with a technique for determining whether this program will be sufficiently accurate for his particular application, as well as providing a means of finding the solution. The input to the program consists of four types of data: (1) computer program control constants, (2) measurements of gas radiance and transmittance at selected wavelengths, (3) tabulations from the literature of gas

  7. Ground-based NIR emission spectroscopy of HD189733b

    CERN Document Server

    Waldmann, I P; Tinetti, G; Griffith, C A; Swain, M R; Deroo, P

    2011-01-01

    Spectroscopic observations of transiting exoplanets are providing an unprecedented view of the atmospheres of planets around nearby stars. As we learn more about the atmospheres of these remote bodies, we begin to build up a clearer picture of their composition and thermal structure. Here we investigate the case of K and L band emissions of the hot-Jupiter HD 189733b. Using the SpeX instrument on the NASA IRTF, we obtained three nights of secondary eclipse data using equivalent settings for all nights. Our sample includes one night previously presented by Swain et al. (2010) which allows for comparability of results. In this publication we present and discuss in detail a greatly improved data-reduction and analysis routine. This, in conjunction with more data, allows us to increase the spectral resolution of our planetary spectrum (R ~ 170-180), leading to a better identifiability of the features present. We confirm the existence of a strong emission at ~3.3 microns which is inconsistent with LTE simulations ...

  8. Optical Emission Spectroscopy Investigation of a Surface Dielectric Barrier Discharge Plasma Aerodynamic Actuator

    Institute of Scientific and Technical Information of China (English)

    LI Ying-Hong; WU Yun; JIA Min; ZHOU Zhang-Wen; GUO Zhi-Gang; PU Yi-Kang

    2008-01-01

    The optical emission spectroscopy of a surface dielectric barrier discharge plasma aerodynamic actuator is investigated with different electrode configurations, applied voltages and driving frequencies. The rotational temperature of N2 (C3IIu) molecule is calculated according to its rotational emission band near 380.5 nm. The average electron energy of the discharge is evaluated by emission intensity ratio of first negative system to second positive system of N2. The rotational temperature is sensitive to the inner space of an electrode pair. The average electron energy shows insensitivity to the applied voltage, the driving frequency and the electrode configuration.

  9. Single photon infrared emission spectroscopy: a study of IR emission from UV laser excited PAHs between 3 and 15 micrometers

    Science.gov (United States)

    Cook, D. J.; Schlemmer, S.; Balucani, N.; Wagner, D. R.; Harrison, J. A.; Steiner, B.; Saykally, R. J.

    1998-01-01

    Single-photon infrared emission spectroscopy (SPIRES) has been used to measure emission spectra from polycyclic aromatic hydrocarbons (PAHs). A supersonic free-jet expansion has been used to provide emission spectra of rotationally cold and vibrationally excited naphthalene and benzene. Under these conditions, the observed width of the 3.3-micrometers (C-H stretch) band resembles the bandwidths observed in experiments in which emission is observed from naphthalene with higher rotational energy. To obtain complete coverage of IR wavelengths relevant to the unidentified infrared bands (UIRs), UV laser-induced desorption was used to generate gas-phase highly excited PAHs. Lorentzian band shapes were convoluted with the monochromator-slit function in order to determine the widths of PAH emission bands under astrophysically relevant conditions. Bandwidths were also extracted from bands consisting of multiple normal modes blended together. These parameters are grouped according to the functional groups mostly involved in the vibration, and mean bandwidths are obtained. These bandwidths are larger than the widths of the corresponding UIR bands. However, when the comparison is limited to the largest PAHs studied, the bandwidths are slightly smaller than the corresponding UIR bands. These parameters can be used to model emission spectra from PAH cations and cations of larger PAHs, which are better candidate carriers of the UIRs.

  10. APPLYING OPEN-PATH OPTICAL SPECTROSCOPY TO HEAVY-DUTY DIESEL EMISSIONS

    Science.gov (United States)

    Non-dispersive infrared absorption has been used to measure gaseous emissions for both stationary and mobile sources. Fourier transform infrared spectroscopy has been used for stationary sources as both extractive and open-path methods. We have applied the open-path method for bo...

  11. 2p3d Resonant X-ray emission spectroscopy of cobalt compounds

    NARCIS (Netherlands)

    van Schooneveld, M.M.

    2013-01-01

    This manuscript demonstrates that 2p3d resonant X-ray emission spectroscopy (RXES) yields unique information on the chemically relevant valence electrons of transition metal atoms or ions. Experimental data on cobalt compounds and several theories were used hand-in-hand. In chapter 1 2p3d RXES was s

  12. The influence of magnetic fields on absorption and emission spectroscopy

    CERN Document Server

    Zhang, Heshou; Richter, Philipp

    2016-01-01

    Spectroscopic observations play essential roles in astrophysics. They are crucial for determining important physical parameters, providing information about the composition of various objects in the universe, as well as depicting motions in the universe. However, spectroscopic studies often do not consider the influence of magnetic fields. In this paper, we explore the influence of magnetic fields on the spectroscopic observations arising from Ground State Alignment (GSA). Synthetic spectra are generated to show the measurable changes of the spectra due to GSA. The influences of atomic alignment on absorption from DLAs, emission from H\\,{\\sc ii} Regions, submillimeter fine-structure lines from star forming regions are presented as examples to illustrate the effect in diffuse gas. Furthermore, we demonstrate the influence of atomic alignment on physical parameters derived from spectral line ratios, such as the alpha-to-iron ratio([X/Fe]), interstellar temperature, and ionization rate. Results in our paper show...

  13. Field-emission spectroscopy of beryllium atoms adsorbed on tungsten

    Energy Technology Data Exchange (ETDEWEB)

    Czyzewski, J.J.; Grzesiak, W.; Krajniak, J. (Politechnika Wroclawska (Poland))

    1981-01-01

    Field emission energy distributions (FEED) have been measured for the beryllium-tungsten (023) adsorption system over the 78-450 K temperature range. A temperature dependence of the normalized half-width, ..delta../d, of FEED peaks changed significantly due to beryllium adsorption; and the curve, ..delta../d vs p, for the Be/W adsorption system was identical in character to the calculated curve based on the free electron model in contrast to the curve for the clean tungsten surface. In the last part of this paper Gadzuk's theory of the resonance-tunneling effect is applied to the beryllium atom on tungsten. Experimental and theoretical curves of the enhancement factor as a function of energy have been discussed.

  14. Lithium loss in the solid electrolyte interphase: Lithium quantification of aged lithium ion battery graphite electrodes by means of laser ablation inductively coupled plasma mass spectrometry and inductively coupled plasma optical emission spectroscopy

    Science.gov (United States)

    Schwieters, Timo; Evertz, Marco; Mense, Maximilian; Winter, Martin; Nowak, Sascha

    2017-07-01

    In this work we present a new method using LA-ICP-MS to quantitatively determine the lithium content in aged graphite electrodes of a lithium ion battery (LIB) by performing total depth profiling. Matrix matched solid external standards are prepared using a solid doping approach to avoid elemental fractionation effects during the measurement. The results are compared and matched to the established ICP-OES technique for bulk quantification after performing a microwave assisted acid digestion. The method is applied to aged graphite electrodes in order to determine the lithium immobilization (= ;Li loss;) in the solid electrolyte interphase after the first cycle of formation. For this, different samples including a reference sample are created to obtain varying thicknesses of the SEI covering the electrode particles. By applying defined charging voltages, an initial lithiation process is performed to obtain specific graphite intercalation compounds (GICs, with target stoichiometries of LiC30, LiC18, LiC12 and LiC6). Afterwards, the graphite electrode is completely discharged to obtain samples without mobile, thus active lithium in its lattice. Taking the amount of lithium into account which originates from the residues of the LiPF6 (dissolved in the carbon components containing electrolyte), it is possible to subtract the amount of lithium in the SEI.

  15. Rapid evaluation of ion thruster lifetime using optical emission spectroscopy

    Science.gov (United States)

    Rock, B. A.; Parsons, M. L.; Mantenieks, M. A.

    1985-01-01

    A major life-limiting phenomenon of electric thrusters is the sputter erosion of discharge chamber components. Thrusters for space propulsion are required to operate for extended periods of time, usually in excess of 10,000 hr. Lengthy and very costly life-tests in high-vacuum facilities have been required in the past to determine the erosion rates of thruster components. Alternative methods for determining erosion rates which can be performed in relatively short periods of time at considerably lower costs are studied. An attempt to relate optical emission intensity from an ion bombarded surface (screen grid) to the sputtering rate of that surface is made. The model used a kinetic steady-state (KSS) approach, balancing the rates of population and depopulation of ten low-lying excited states of the sputtered molybdenum atom (MoI) with those of the ground state to relate the spectral intensities of the various transitions of the MoI to the population densities. Once this is accomplished, the population density can be related to the sputting rate of the target. Radiative and collisional modes of excitation and decay are considered. Since actual data has not been published for MoI excitation rate and decay constants, semiempirical equations are used. The calculated sputtering rate and intensity is compared to the measured intensity and sputtering rates of the 8 and 30 cm ion thrusters.

  16. The influence of magnetic fields on absorption and emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Heshou; Yan, Huirong [Deutsches Elektronen-Synchrotron (DESY), Zeuthen (Germany); Potsdam Univ. (Germany). Inst. fuer Physik und Astronomie; Richter, Philipp [Potsdam Univ. (Germany). Inst. fuer Physik und Astronomie; Leibniz-Institut fuer Astrophysik Potsdam (AIP) (Germany)

    2016-10-15

    Spectroscopic observations play essential roles in astrophysics. They are crucial for determining important physical parameters, providing information about the composition of various objects in the universe, as well as depicting motions in the universe. However, spectroscopic studies often do not consider the influence of magnetic fields. In this paper, we explore the influence of magnetic fields on the spectroscopic observations arising from Ground State Alignment (GSA). Synthetic spectra are generated to show the measurable changes of the spectra due to GSA. The influences of atomic alignment on absorption from DLAs, emission from H II Regions, submillimeter fine-structure lines from star forming regions are presented as examples to illustrate the effect in diffuse gas. Furthermore, we demonstrate the influence of atomic alignment on physical parameters derived from spectral line ratios, such as the alpha-to-iron ratio([X/Fe]), interstellar temperature, and ionization rate. Results in our paper show that due to GSA, magnetic fields will affect the spectra of diffuse gas with high signal-to-noise(S/N) ratio under the condition that photon-excitation is much more efficient than thermal collision.

  17. Identification of microcrystalline rocks using thermal emission spectroscopy

    Science.gov (United States)

    Hardgrove, C. J.; Rogers, D.; Glotch, T. D.; Arnold, J. A.

    2015-12-01

    High-silica deposits on Mars have been discovered from orbit (Holden Crater, Mawrth Vallis) and from landed surface missions to both Gusev Crater (Spirit) and Gale Crater (Curiosity). The character of these silica deposits can be used to understand both the depositional environment (i.e. fumarole vs. sinter) and/or diagenetic process. Initial work has shown that, in the case of opaline silica, there are differences in spectral shape that may be related to surface textural features imparted during formation or post-depositional alteration. Due to the increasing importance of understanding microcrystalline deposits on Mars, here, we study the effects of crystal size and surface roughness on thermal infrared emission spectra of micro- and macro-crystalline quartz. The spectra of chert and macro-crystalline quartz have significant differences in both spectral contrast, and in the rounded doublet between ~1000-1250 cm-1, which can shift and appear less rounded in microcrystalline samples. We find that microcrystalline minerals exhibit naturally rough surfaces compared to their macrocrystalline counterparts at the 10 micron scale; and that this roughness causes distinct spectral differences within the Reststrahlen bands. We find that surface roughness, if rough on the scale of the wavelengths where the wavelength-dependent absorption coefficient (k) is large, can cause not only decreased spectral contrast, but also substantial changes in spectral shape. The spectral shape differences are small enough that the composition of the material is still recognizable, but large enough such that a roughness effect could be detected. We find that my studying the thermal infrared spectral character of the sample, it may be possible to make general inferences about microcrystallinity, and thus aid in the potential reconstruction of sedimentary rock diagenesis.

  18. X-ray photo-emission and energy dispersive spectroscopy of HA coated titanium

    Energy Technology Data Exchange (ETDEWEB)

    Drummond, J.L.; Steinberg, A.D. [Univ. of Illinois, Chicago, IL (United States); Krauss, A.R. [Argonne National Lab., IL (United States)] [and others

    1997-08-01

    The purpose of this study was to determine the chemical composition changes of hydroxyapatite (HA) coated titanium using surface analysis (x-ray photo-emission) and bulk analysis (energy dispersive spectroscopy). The specimens examined were controls, 30 minutes and 3 hours aged specimens in distilled water or 0.2M sodium phosphate buffer (pH 7.2) at room temperature. Each x-ray photo-emission cycle consisted of 3 scans followed by argon sputtering for 10 minutes for a total of usually 20 cycles, corresponding to a sampling depth of {approximately} 1500 {angstrom}. The energy dispersive spectroscopy analysis was on a 110 by 90 {mu}m area for 500 sec. Scanning electron microscopy examination showed crystal formation (3P{sub 2}O{sub 5}*2CAO*?H{sub 2}O by energy dispersive spectroscopy analysis) on the HA coating for the specimens aged in sodium phosphate buffer. The x-ray photo-emission results indicated the oxidation effect of water on the titanium (as TiO{sub 2}) and the effect of the buffer to increase the surface concentration of phosphorous. No differences in the chemical composition were observed by energy dispersive spectroscopy analysis. The crystal growth was only observed for the sodium phosphate buffer specimens and only on the HA surface.

  19. Excitation emission and time-resolved fluorescence spectroscopy of selected varnishes used in historical musical instruments.

    Science.gov (United States)

    Nevin, Austin; Echard, Jean-Philippe; Thoury, Mathieu; Comelli, Daniela; Valentini, Gianluca; Cubeddu, Rinaldo

    2009-11-15

    The analysis of various varnishes from different origins, which are commonly found on historical musical instruments was carried out for the first time with both fluorescence excitation emission spectroscopy and laser-induced time-resolved fluorescence spectroscopy. Samples studied include varnishes prepared using shellac, and selected diterpenoid and triterpenoid resins from plants, and mixtures of these materials. Fluorescence excitation emission spectra have been collected from films of naturally aged varnishes. In parallel, time-resolved fluorescence spectroscopy of varnishes provides means for discriminating between short- (less than 2.0 ns) and long-lived (greater than 7.5 ns) fluorescence emissions in each of these complex materials. Results suggest that complementary use of the two non destructive techniques allows a better understanding of the main fluorophores responsible for the emission in shellac, and further provides means for distinguishing the main classes of other varnishes based on differences in fluorescence lifetime behaviour. Spectrofluorimetric data and time resolved spectra presented here may form the basis for the interpretation of results from future in situ fluorescence examination and time resolved fluorescence imaging of varnished musical instruments.

  20. Kinetic model of atomic and molecular emissions in laser-induced breakdown spectroscopy of organic compounds.

    Science.gov (United States)

    Ma, Qianli; Dagdigian, Paul J

    2011-07-01

    A kinetic model previously developed to predict the relative intensities of atomic emission lines in laser-induced breakdown spectroscopy has been extended to include processes related to CN and C(2) molecular emissions. Simulations with this model were performed to predict the relative excited-state populations. The results from the simulations are compared with experimentally determined excited-state populations from 1,064 nm laser irradiation of organic residues on aluminum foil. The model reasonably predicts the relative intensity of the molecular emissions. Significantly, the model reproduces the vastly different temporal profiles of the atomic and molecular emissions. The latter are found to extend to much longer times after the laser pulse, and this appears to be due to the increasing concentration of the molecules versus time. From the simulations, the important processes affecting the CN and C(2) concentrations are identified.

  1. Hole emission from Ge/Si quantum dots studied by time-resolved capacitance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kapteyn, C.M.A.; Lion, M.; Heitz, R.; Bimberg, D. [Technische Univ. Berlin (Germany). Inst. fuer Festkoerperphysik; Miesner, C.; Asperger, T.; Brunner, K.; Abstreiter, G. [Technische Univ. Muenchen, Garching (Germany). Walter-Schottky-Inst. fuer Physikalische Grundlagen der Halbleiterelektronik

    2001-03-01

    Emission of holes from self-organized Ge quantum dots (QDs) embedded in Si Schottky diodes is studied by time-resolved capacitance spectroscopy (DLTS). The DLTS signal is rather broad and depends strongly on the filling and detection bias conditions. The observed dependence is interpreted in terms of carrier emission from many-hole states of the QDs. The activation energies obtained from the DLTS measurements are a function of the amount of stored charge and the position of the Fermi level in the QDs. (orig.)

  2. Determination of heavy metals in solid emission and immission samples using atomic absorption spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Fara, M.; Novak, F. [EGU Prague, PLC, Bichovice, Prague (Czechoslovakia)

    1995-12-01

    Both flame and electrothermal methods of atomic absorption spectroscopy (AAS) have been applied to the determination of Al, As, Be, Ca, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, TI, Se, V and Zn in emission and emission (deposition) samples decomposed in open PTFE test-tubes by individual fuming-off hydrofluoric, perchloroic and nitric acid. An alternative hydride technique was also used for As and Se determination and Hg was determined using a self-contained AAS analyzer. A graphite platform proved good to overcome non-spectral interferences in AAS-ETA. Methods developed were verified by reference materials (inc. NBS 1633a).

  3. GROUND-BASED NEAR-INFRARED EMISSION SPECTROSCOPY OF HD 189733B

    Energy Technology Data Exchange (ETDEWEB)

    Waldmann, I. P.; Tinetti, G. [Department of Physics and Astronomy, University College London, Gower Street, WC1E 6BT (United Kingdom); Drossart, P. [LESIA, Observatoire de Paris, CNRS, Universit Pierre et Marie Curie, Universit Paris-Diderot. 5 place Jules Janssen, 92195 Meudon (France); Swain, M. R.; Deroo, P. [Jet Propulsion Laboratory, California Institute of Technology, 4800 Oak Grove Drive, Pasadena, CA 91109-8099 (United States); Griffith, C. A., E-mail: ingo@star.ucl.ac.uk [Department of Planetary Sciences, University of Arizona, 1629 E. University Blvd, Tucson, AZ 85721 (United States)

    2012-01-01

    We investigate the K- and L-band dayside emission of the hot-Jupiter HD 189733b with three nights of secondary eclipse data obtained with the SpeX instrument on the NASA Infrared Telescope Facility. The observations for each of these three nights use equivalent instrument settings and the data from one of the nights have previously been reported by Swain et al. We describe an improved data analysis method that, in conjunction with the multi-night data set, allows increased spectral resolution (R {approx} 175) leading to high-confidence identification of spectral features. We confirm the previously reported strong emission at {approx}3.3 {mu}m and, by assuming a 5% vibrational temperature excess for methane, we show that non-LTE emission from the methane {nu}{sub 3} branch is a physically plausible source of this emission. We consider two possible energy sources that could power non-LTE emission and additional modeling is needed to obtain a detailed understanding of the physics of the emission mechanism. The validity of the data analysis method and the presence of strong 3.3 {mu}m emission are independently confirmed by simultaneous, long-slit, L-band spectroscopy of HD 189733b and a comparison star.

  4. Investigation of microplasma discharge in sea water for optical emission spectroscopy

    Science.gov (United States)

    Gamaleev, Vladislav; Okamura, Yo; Kitamura, Kensuke; Hashimoto, Yusuke; Oh, Jun-Seok; Furuta, Hiroshi; Hatta, Akimitsu

    2016-07-01

    Microplasma discharge in sea water for optical emission spectroscopy was investigated using a needle-to-plane electrode system. The electrodes of a Pd needle and a Pt plate were placed with a gap of 25 µm in typical artificial sea water or locally sampled natural deep sea water. A pulse current source, consisting of a MOSFET switch, a capacitor, an inductor and the resistance of the sea water between the electrodes, was used. The circuit parameters were optimized to decrease the breakdown voltage and the spark duration to suppress erosion of the electrodes. Using a microgap configuration, spark discharges were reproducibly ignited in the highly conductive sea water at low breakdown voltages. The ignition of spark discharges required not only a critical voltage sufficient for breakdown, but also a critical energy for preheating of the sea water, sufficient for bubble formation. The possibility of using optical emission spectroscopy of microplasma in water is shown for identifying elemental composition of sea water.

  5. Characterization by acoustic emission and electrochemical impedance spectroscopy of the cathodic disbonding of Zn coating

    Energy Technology Data Exchange (ETDEWEB)

    Amami, Souhail [Universite de Technologie de Compiegne, Departement de Genie Mecanique, Laboratoire Roberval, UMR 6066 du CNRS, B.P. 20529, 60206 Compiegne Cedex (France)], E-mail: souhail.amami@utc.fr; Lemaitre, Christian; Laksimi, Abdelouahed; Benmedakhene, Salim [Universite de Technologie de Compiegne, Departement de Genie Mecanique, Laboratoire Roberval, UMR 6066 du CNRS, B.P. 20529, 60206 Compiegne Cedex (France)

    2010-05-15

    Galvanized steel has been tested in a synthetic sea water solution under different cathodic overprotection conditions. The generated hydrogen flux caused the damage of the metal-zinc interface and led to a progressive coating detachment. Scanning electron microscopy, electrochemical impedance spectroscopy and acoustic emission technique were used to characterize the damage chronology under different cathodic potentials. A damage mechanism was proposed and the acoustic signature related to the coating degradation was statistically identified using clustering techniques.

  6. Eye-safe infrared laser-induced breakdown spectroscopy (LIBS) emissions from energetic materials

    Science.gov (United States)

    Brown, Ei E.; Hömmerich, Uwe; Yang, Clayton C.; Jin, Feng; Trivedi, Sudhir B.; Samuels, Alan C.

    2016-05-01

    Laser-induced breakdown spectroscopy is a powerful diagnostic tool for detection of trace elements by monitoring the atomic and ionic emission from laser-induced plasmas. Besides elemental emissions from conventional UV-Vis LIBS, molecular LIBS emission signatures of the target compounds were observed in the long-wave infrared (LWIR) region in recent studies. Most current LIBS studies employ the fundamental Nd:YAG laser output at 1.064 μm, which has extremely low eye-damage threshold. In this work, comparative LWIR-LIBS emissions studies using traditional 1.064 μm pumping and eye-safe laser wavelength at 1.574 μm were performed on several energetic materials for applications in chemical, biological, and explosive (CBE) sensing. A Q-switched Nd: YAG laser operating at 1.064 μm and the 1.574 μm output of a pulsed Nd:YAG pumped Optical Parametric Oscillator were employed as the excitation sources. The investigated energetic materials were studied for the appearance of LWIR-LIBS emissions (4-12 μm) that are directly indicative of oxygenated breakdown products as well as partially dissociated and recombination molecular species. The observed molecular IR LIBS emission bands showed strong correlation with FTIR absorption spectra of the studied materials for 1.064 μm and 1.574 μm pump wavelengths.

  7. Comparison endpoint study of process plasma and secondary electron beam exciter optical emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Stephan Thamban, P. L.; Yun, Stuart; Padron-Wells, Gabriel; Hosch, Jimmy W.; Goeckner, Matthew J. [Department of Mechanical Engineering, University of Texas at Dallas, 800W Campbell Road, Richardson, Texas 75080 (United States); Department of Electrical Engineering, University of Texas at Dallas, 800W Campbell Road, Richardson, Texas 75080 (United States); Verity Instruments, Inc., 2901 Eisenhower Street, Carrollton, Texas 75007 (United States); Department of Mathematical Sciences, University of Texas at Dallas, 800 W Campbell Road, Richardson, Texas 75080 (United States)

    2012-11-15

    Traditionally process plasmas are often studied and monitored by optical emission spectroscopy. Here, the authors compare experimental measurements from a secondary electron beam excitation and direct process plasma excitation to discuss and illustrate its distinctiveness in the study of process plasmas. They present results that show excitations of etch process effluents in a SF{sub 6} discharge and endpoint detection capabilities in dark plasma process conditions. In SF{sub 6} discharges, a band around 300 nm, not visible in process emission, is observed and it can serve as a good indicator of etch product emission during polysilicon etches. Based on prior work reported in literature the authors believe this band is due to SiF{sub 4} gas phase species.

  8. Spatially resolved optical-emission spectroscopy of a radio-frequency driven iodine plasma source

    Science.gov (United States)

    Dedrick, James; Doyle, Scott; Grondein, Pascaline; Aanesland, Ane

    2016-09-01

    Iodine is of interest for potential use as a propellant for spacecraft propulsion, and has become attractive as a replacement to xenon due to its similar mass and ionisation potential. Optical emission spectroscopy has been undertaken to characterise the emission from a low-pressure, radio-frequency driven inductively coupled plasma source operating in iodine with respect to axial distance across its transverse magnetic filter. The results are compared with axial profiles of the electron temperature and density for identical source conditions, and the spatial distribution of the emission intensity is observed to be closely correlated with the electron temperature. This work has been done within the LABEX Plas@Par project, and received financial state aid managed by the ``Agence Nationale de la Recherche'', as part of the ``Programme d'Investissements d'Avenir'' under the reference ANR-11-IDEX-0004-02.

  9. Characterisation of a micro-plasma device sensor using electrical measurements and emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Mariotti, D

    2002-04-01

    This thesis reports on research undertaken on the characterisation of a micro-plasma device to be used for gas analysis by mean of plasma emission spectroscopy. The work covers aspects related to the micro-plasma electrical and optical emission parameters, and their importance for the utilisation of the micro-plasma device in gas analysis. Experimental results have been used to analyse the fundamental micro-plasma processes and to develop a model, which could provide additional information. This dissertation contains a general literature review of topics related to plasma physics, plasma emission spectroscopy, gas analysis (chemical analysis and artificial olfaction) and other micro-plasma applications. Experimental work focuses on two main areas: electrical measurements and emission measurements. Firstly, electrical measurements are taken and interpretations are given. Where necessary, new theoretical treatments are suggested in order to describe better the physical phenomena. Plasma emission has been considered under different working conditions. This allowed the characterisation of the micro-plasma emission and also a better understanding of the micro-plasma processes. On the basis of the experimental data obtained and other assumptions a model has been developed. A computer simulation based on this model provided additional useful information on the micro- plasma behaviour. The first fundamental implication of this new research is the peculiar behaviour of the micro-plasma. This micro-plasma exhibited deviations from Paschen law and strong dependency on cathode material, which contributed to the formation of a low current stable regime. These results have been followed by physical interpretations and theoretical descriptions. The second implication is the establishment of the boundaries and of the influencing parameters for plasma emission spectroscopy as an analytical tool in this particular micro-plasma. From the applied perspective this study has shown that

  10. Ultrafast Time-Resolved Hard X-Ray Emission Spectroscopy on a Tabletop

    Science.gov (United States)

    Miaja-Avila, Luis; O'Neil, Galen C.; Joe, Young I.; Alpert, Bradley K.; Damrauer, Niels H.; Doriese, William B.; Fatur, Steven M.; Fowler, Joseph W.; Hilton, Gene C.; Jimenez, Ralph; Reintsema, Carl D.; Schmidt, Daniel R.; Silverman, Kevin L.; Swetz, Daniel S.; Tatsuno, Hideyuki; Ullom, Joel N.

    2016-07-01

    Experimental tools capable of monitoring both atomic and electronic structure on ultrafast (femtosecond to picosecond) time scales are needed for investigating photophysical processes fundamental to light harvesting, photocatalysis, energy and data storage, and optical display technologies. Time-resolved hard x-ray (>3 keV ) spectroscopies have proven valuable for these measurements due to their elemental specificity and sensitivity to geometric and electronic structures. Here, we present the first tabletop apparatus capable of performing time-resolved x-ray emission spectroscopy. The time resolution of the apparatus is better than 6 ps. By combining a compact laser-driven plasma source with a highly efficient array of microcalorimeter x-ray detectors, we are able to observe photoinduced spin changes in an archetypal polypyridyl iron complex [Fe (2 ,2'-bipyridine)3]2 + and accurately measure the lifetime of the quintet spin state. Our results demonstrate that ultrafast hard x-ray emission spectroscopy is no longer confined to large facilities and now can be performed in conventional laboratories with 10 times better time resolution than at synchrotrons. Our results are enabled, in part, by a 100- to 1000-fold increase in x-ray collection efficiency compared to current techniques.

  11. Boosting persistence time of laser-induced plasma by electric arc discharge for optical emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Eschlböck-Fuchs, S., E-mail: simon.eschlboeck-fuchs@jku.at [Christian Doppler Laboratory for Laser-Assisted Diagnostics, Institute of Applied Physics, Johannes Kepler University Linz, A-4040 Linz (Austria); Kolmhofer, P.J.; Bodea, M.A.; Hechenberger, J.G.; Huber, N. [Christian Doppler Laboratory for Laser-Assisted Diagnostics, Institute of Applied Physics, Johannes Kepler University Linz, A-4040 Linz (Austria); Rössler, R. [voestalpine Stahl GmbH, A-4031 Linz (Austria); Pedarnig, J.D., E-mail: johannes.pedarnig@jku.at [Christian Doppler Laboratory for Laser-Assisted Diagnostics, Institute of Applied Physics, Johannes Kepler University Linz, A-4040 Linz (Austria)

    2015-07-01

    Plasma induced by nanosecond laser ablation is re-excited by a pulsed electric discharge and the parameters and optical emission of the plasma are measured. The discharge is a low-voltage and high-current electric arc that is triggered by the laser-induced plasma and slowly decaying with time. The optical emission of such combined plasma lasts up to several milliseconds which is much longer than without re-excitation (μs range). The emission spectra of re-excited plasma measured on different sample materials show higher line intensities than spectra measured by conventional laser-induced breakdown spectroscopy (LIBS). Moreover, emission lines of fluorine (spectral range 683–691 nm) and sulfur (range 520–550 nm) not detected by conventional LIBS become easily detectable with the combined plasma. The concentration of major components in metallurgical slags, as determined by calibration-free LIBS, agrees very well to the reference data evaluating the spectra taken from re-excited plasma. - Highlights: • Persistence time of laser-induced plasma in air is increased from ~ 10 μs to ~ 1 ms. • Laser-induced plasma triggers an electric arc discharge that boosts the plasma. • The combined laser-arc plasma is in LTE state over very long time (ms range). • CF-LIBS method delivers accurate results evaluating spectra of combined plasma. • Emission from S and F, not detected by LIBS, is detected with combined plasma.

  12. [Photodissociation of Acetylene and Acetone using Step-Scan Time-Resolved FTIR Emission Spectroscopy

    Science.gov (United States)

    McLaren, Ian A.; Wrobel, Jacek D.

    1997-01-01

    The photodissociation of acetylene and acetone was investigated as a function of added quenching gas pressures using step-scan time-resolved FTIR emission spectroscopy. Its main components consist of Bruker IFS88, step-scan Fourier Transform Infrared (FTIR) spectrometer coupled to a flow cell equipped with Welsh collection optics. Vibrationally excited C2H radicals were produced from the photodissociation of acetylene in the unfocused experiments. The infrared (IR) emission from these excited C2H radicals was investigated as a function of added argon pressure. Argon quenching rate constants for all C2H emission bands are of the order of 10(exp -13)cc/molecule.sec. Quenching of these radicals by acetylene is efficient, with a rate constant in the range of 10(exp -11) cc/molecule.sec. The relative intensity of the different C2H emission bands did not change with the increasing argon or acetylene pressure. However, the overall IR emission intensity decreased, for example, by more than 50% when the argon partial pressure was raised from 0.2 to 2 Torr at fixed precursor pressure of 160mTorr. These observations provide evidence for the formation of a metastable C2H2 species, which are collisionally quenched by argon or acetylene. Problems encountered in the course of the experimental work are also described.

  13. Lithium-ion battery electrolyte emissions analyzed by coupled thermogravimetric/Fourier-transform infrared spectroscopy

    Science.gov (United States)

    Bertilsson, Simon; Larsson, Fredrik; Furlani, Maurizio; Albinsson, Ingvar; Mellander, Bengt-Erik

    2017-10-01

    In the last few years the use of Li-ion batteries has increased rapidly, powering small as well as large applications, from electronic devices to power storage facilities. The Li-ion battery has, however, several safety issues regarding occasional overheating and subsequent thermal runaway. During such episodes, gas emissions from the electrolyte are of special concern because of their toxicity, flammability and the risk for gas explosion. In this work, the emissions from heated typical electrolyte components as well as from commonly used electrolytes are characterized using FT-IR spectroscopy and FT-IR coupled with thermogravimetric (TG) analysis, when heating up to 650 °C. The study includes the solvents EC, PC, DEC, DMC and EA in various single, binary and ternary mixtures with and without the LiPF6 salt, a commercially available electrolyte, (LP71), containing EC, DEC, DMC and LiPF6 as well as extracted electrolyte from a commercial 6.8 Ah Li-ion cell. Upon thermal heating, emissions of organic compounds and of the toxic decomposition products hydrogen fluoride (HF) and phosphoryl fluoride (POF3) were detected. The electrolyte and its components have also been extensively analyzed by means of infrared spectroscopy for identification purposes.

  14. Quantifying Fugitive Methane Emissions at an Underground Coal Fire Using Cavity Ring-Down Spectroscopy Technology

    Science.gov (United States)

    Fleck, D.; Gannon, L.; Kim-Hak, D.; Ide, T.

    2016-12-01

    Understanding methane emissions is of utmost importance due to its greenhouse warming potential. Methane emissions can occur from a variety of natural and anthropogenic sources which include wetlands, landfills, oil/gas/coal extraction activities, underground coal fires, and natural gas distribution systems. Locating and containing these emissions are critical to minimizing their environmental impacts and economically beneficial when retrieving large fugitive amounts. In order to design a way to mitigate these methane emissions, they must first be accurately quantified. One such quantification method is to measure methane fluxes, which is a measurement technique that is calculated based on rate of gas accumulation in a known chamber volume over methane seepages. This allows for quantification of greenhouse gas emissions at a localized level (sub one meter) that can complement remote sensing and other largescale modeling techniques to further paint the picture of emission points. High performance analyzers are required to provide both sufficient temporal resolution and precise concentration measurements in order to make these measurements over only minutes. A method of measuring methane fluxes was developed using the latest portable, battery-powered Cavity Ring-Down Spectroscopy analyzer from Picarro (G4301). In combination with a mobile accumulation chamber, the instrument allows for rapid measurement of methane and carbon dioxide fluxes over wide areas. For this study, methane fluxes that were measured at an underground coal fire near the Four Corners region using the Picarro analyzer are presented. The flux rates collected demonstrate the ability for the analyzer to detect methane fluxes across many orders of magnitude. Measurements were accompanied by simultaneously geotagging the measurements with GPS to georeferenced the data. Methane flux data were instrumental in our ability to characterize the extent and the migration of the underground fire. In the future

  15. A rapid screening method for heavy metals in biological materials by emission spectroscopy.

    Science.gov (United States)

    Blacklock, E C; Sadler, P A

    1981-06-02

    A semi-quantitative screening method for heavy metals in biological material is described. The metals are complexed with ammonium pyrrolidine dithiocarbamate, sodium diethyl dithiocarbamate and potassium sodium tartrate. The solutions are adjusted to pH 4 and then extracted into chloroform. The chloroform phase is evaporated onto a matrix mixture of lithium fluoride and graphite. The sample is analysed by direct current arc emission spectroscopy using a 3 metre grating spectrograph. The spectra are recorded on a photographic plate. The method is developed on aqueous and spiked samples and then applied to in vivo samples containing toxic levels of heavy metals. Atomic absorption spectroscopy is used to check standard concentrations and to monitor the efficiency of the extraction procedure.

  16. Excitation-emission matrices and synchronous fluorescence spectroscopy for the diagnosis of gastrointestinal cancers

    Science.gov (United States)

    Genova, Ts; Borisova, E.; Penkov, N.; Vladimirov, B.; Zhelyazkova, A.; Avramov, L.

    2016-06-01

    We report the development of an improved fluorescence technique for cancer diagnostics in the gastrointestinal tract. We investigate the fluorescence of ex vivo colorectal (cancerous and healthy) tissue samples using excitation-emission matrix (EEM) and synchronous fluorescence spectroscopy (SFS) steady-state approaches. The obtained results are processed for revealing characteristic fluorescence spectral features with a valuable diagnostic meaning. The main tissue fluorophores, contributing to the observed fluorescence, are tyrosine, tryptophan, NADH, FAD, collagen and elastin. Based on the results of the Mann-Whitney test as useful parameters for differentiation of gastrointestinal cancer from normal mucosa, we suggest using excitation wavelengths in the range 300 - 360 nm for fluorescence spectroscopy and wavelengths intervals of 60 nm and 90 nm for SFS.

  17. Assessing topographic cutaneous autofluorescence variation using fluorescence UV and visible excitation emission matrix (EEM) spectroscopy

    Science.gov (United States)

    Zhao, Jianhua; Zandi, Soodabeh; Feng, Florina; Zeng, Haishan; McLean, David I.; Lui, Harvey

    2011-03-01

    Cutaneous autofluorescence properties were systematically studied using fluorescence excitation emission matrix spectroscopy. Twenty-six healthy subjects with a mean age of 34 (range 21-74) participated in this study. The fluorescence of major skin fluorophores such as tryptophan, collagen, elastin and NADH could be readily identified. On average, facial skin shows strong tryptophan and measurable porphyrin fluorescence; the palm and nail show strong tryptophan and keratin fluorescence. These results demonstrate that regional topographic variations exist not only in the amount of fluorescence but also in the relative distribution of fluorophores in normal skin. Moreover this provides a basis for future interpretation of autofluorescence in diseased skin.

  18. Scrape-off layer-induced beam density fluctuations and their effect on beam emission spectroscopy

    Science.gov (United States)

    Moulton, D.; Marandet, Y.; Tamain, P.; Dif-Pradalier, G.

    2015-07-01

    A statistical model is presented to calculate the magnitude of beam density fluctuations generated by a turbulent scrape-off layer (SOL). It is shown that the SOL can induce neutral beam density fluctuations of a similar magnitude to the plasma density fluctuations in the core, potentially corrupting beam emission spectroscopy measurements. The degree of corruption is quantified by combining simulations of beam and plasma density fluctuations inside a simulated measurement window. A change in pitch angle from the separatrix to the measurement window is found to reduce the effect of beam fluctuations, whose largest effect is to significantly reduce the measured correlation time.

  19. Application of {sup 57}Co emission Moessbauer spectroscopy to studying biocomplexes in frozen solutions

    Energy Technology Data Exchange (ETDEWEB)

    Kamnev, A. A., E-mail: aakamnev@ibppm.sgu.ru [Laboratory of Biochemistry of Plant-Bacterial Symbioses, Institute of Biochemistry and Physiology of Plants and Microorganisms, Russian Academy of Sciences (Russian Federation); Kulikov, L. A.; Perfiliev, Yu. D. [M.V. Lomonosov Moscow State University, Laboratory of Nuclear Chemistry Techniques, Department of Radiochemistry, Faculty of Chemistry (Russian Federation); Antonyuk, L. P. [Laboratory of Biochemistry of Plant-Bacterial Symbioses, Institute of Biochemistry and Physiology of Plants and Microorganisms, Russian Academy of Sciences (Russian Federation); Kuzmann, E.; Vertes, A. [Eoetvoes Lorand University, Research Group for Nuclear Techniques in Structural Chemistry, Hungarian Academy of Sciences, Department of Nuclear Chemistry (Hungary)

    2005-09-15

    Emission Moessbauer spectroscopy with the {sup 57}Co isotope was used to study very dilute rapidly frozen aqueous solutions of cobalt(II) complexes with low-molecular-weight biomolecules (aromatic amino acids - anthranilic acid and L-tryptophan) and within a sophisticated biopolymer, bacterial glutamine synthetase, a key enzyme of nitrogen metabolism. The appearance of after-effects of the {sup 57}Co{sup {yields}57}Fe nuclear transformation as well as the coordination properties of the cation and the ligands in the complexes are discussed on the basis of their Moessbauer parameters.

  20. Remote gas analysis of aircraft exhausts using FTIR-emission-spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Heland, J.; Schaefer, K. [Fraunhofer Inst. for Atmospheric Environmental Research, Garmisch-Partenkirchen (Germany)

    1997-12-31

    FITR emission spectroscopy as a remote sensing multi-component analyzing technique was investigated to determine the composition of aircraft exhausts at ground level. A multi-layer radiative transfer interpretation software based on a line-by-line computer algorithm using the HITRAN data base was developed. Measurements were carried out with different engine types to determine the traceable gas species and their detection limits. Finally validation measurements were made to compare the results of the system to those of conventional equipment. (author) 8 refs.

  1. VUV emission spectroscopy combined with H− density measurements in the ion source Prometheus I

    OpenAIRE

    Aleiferis, S.; Laulainen, Janne; Svarnas, P.; Tarvainen, Olli; Bacal, M.; Béchu, S.

    2017-01-01

    “Prometheus I” is a volume H− negative ion source, driven by a network of dipolar electron cyclotron resonance (ECR; 2.45 GHz) modules. The vacuum-ultraviolet (VUV) emission spectrum of low-temperature hydrogen plasmas may be related to molecular and atomic processes involved directly or indirectly in the production of negative ions. In this work, VUV spectroscopy has been performed in the above source, Prometheus I, both in the ECR zones and the bulk (far from ECR zones and surfaces) plasma....

  2. Application of 57Co emission Mössbauer spectroscopy to studying biocomplexes in frozen solutions

    Science.gov (United States)

    Kamnev, A. A.; Kulikov, L. A.; Perfiliev, Yu. D.; Antonyuk, L. P.; Kuzmann, E.; Vértes, A.

    2005-09-01

    Emission Mössbauer spectroscopy with the 57Co isotope was used to study very dilute rapidly frozen aqueous solutions of cobalt(II) complexes with low-molecular-weight biomolecules (aromatic amino acids anthranilic acid and L-tryptophan) and within a sophisticated biopolymer, bacterial glutamine synthetase, a key enzyme of nitrogen metabolism. The appearance of after-effects of the 57Co→57Fe nuclear transformation as well as the coordination properties of the cation and the ligands in the complexes are discussed on the basis of their Mössbauer parameters.

  3. Characterization of dielectric barrier discharge in air applying current measurement, numerical simulation and emission spectroscopy

    CERN Document Server

    Rajasekaran, Priyadarshini; Awakowicz, Peter

    2012-01-01

    Dielectric barrier discharge (DBD) in air is characterized applying current measurement, numerical simulation and optical emission spectroscopy (OES). For OES, a non-calibrated spectrometer is used. This diagnostic method is applicable when cross-sectional area of the active plasma volume and current density can be determined. The nitrogen emission in the spectral range of 380 nm- 406 nm is used for OES diagnostics. Electric field in the active plasma volume is determined applying the measured spectrum, well-known Frank-Condon factors for nitrogen transitions and numerically- simulated electron distribution functions. The measured electric current density is used for determination of electron density in plasma. Using the determined plasma parameters, the dissociation rate of nitrogen and oxygen in active plasma volume are calculated, which can be used by simulation of the chemical kinetics.

  4. X-ray absorption and X-ray emission spectroscopy theory and applications

    CERN Document Server

    Lamberti, Carlo

    2016-01-01

    During the last two decades, remarkable and often spectacular progress has been made in the methodological and instrumental aspects of x–ray absorption and emission spectroscopy. This progress includes considerable technological improvements in the design and production of detectors especially with the development and expansion of large-scale synchrotron reactors All this has resulted in improved analytical performance and new applications, as well as in the perspective of a dramatic enhancement in the potential of x–ray based analysis techniques for the near future. This comprehensive two-volume treatise features articles that explain the phenomena and describe examples of X–ray absorption and emission applications in several fields, including chemistry, biochemistry, catalysis, amorphous and liquid systems, synchrotron radiation, and surface phenomena. Contributors explain the underlying theory, how to set up X–ray absorption experiments, and how to analyze the details of the resulting spectra. X-R...

  5. LZIFU: an emission-line fitting toolkit for integral field spectroscopy data

    CERN Document Server

    Ho, I-Ting; Groves, Brent; Rich, Jeffrey A; Rupke, David S N; Hampton, Elise; Kewley, Lisa J; Bland-Hawthorn, Joss; Croom, Scott M; Richards, Samuel; Schaefer, Adam L; Sharp, Rob; Sweet, Sarah M

    2016-01-01

    We present LZIFU (LaZy-IFU), an IDL toolkit for fitting multiple emission lines simultaneously in integral field spectroscopy (IFS) data. LZIFU is useful for the investigation of the dynamical, physical and chemical properties of gas in galaxies. LZIFU has already been applied to many world-class IFS instruments and large IFS surveys, including the Wide Field Spectrograph, the new Multi Unit Spectroscopic Explorer (MUSE), the Calar Alto Legacy Integral Field Area (CALIFA) survey, the Sydney-Australian-astronomical-observatory Multi-object Integral-field spectrograph (SAMI) Galaxy Survey. Here we describe in detail the structure of the toolkit, and how the line fluxes and flux uncertainties are determined, including the possibility of having multiple distinct kinematic components. We quantify the performance of LZIFU, demonstrating its accuracy and robustness. We also show examples of applying LZIFU to CALIFA and SAMI data to construct emission line and kinematic maps, and investigate complex, skewed line prof...

  6. Optical Emission Spectroscopy of an Atmospheric Pressure Plasma Jet During Tooth Bleaching Gel Treatment.

    Science.gov (United States)

    Šantak, Vedran; Zaplotnik, Rok; Tarle, Zrinka; Milošević, Slobodan

    2015-11-01

    Optical emission spectroscopy was performed during atmospheric pressure plasma needle helium jet treatment of various tooth-bleaching gels. When the gel sample was inserted under the plasma plume, the intensity of all the spectral features increased approximately two times near the plasma needle tip and up to two orders of magnitude near the sample surface. The color change of the hydroxylapatite pastille treated with bleaching gels in conjunction with the atmospheric pressure plasma jet was found to be in correlation with the intensity of OH emission band (309 nm). Using argon as an additive to helium flow (2 L/min), a linear increase (up to four times) of OH intensity and, consequently, whitening (up to 10%) of the pastilles was achieved. An atmospheric pressure plasma jet activates bleaching gel, accelerates OH production, and accelerates tooth bleaching (up to six times faster).

  7. Laser-induced optical breakdown spectroscopy of polymer materials based on evaluation of molecular emission bands

    Science.gov (United States)

    Trautner, Stefan; Jasik, Juraj; Parigger, Christian G.; Pedarnig, Johannes D.; Spendelhofer, Wolfgang; Lackner, Johannes; Veis, Pavel; Heitz, Johannes

    2017-03-01

    Laser-induced breakdown spectroscopy (LIBS) for composition analysis of polymer materials results in optical spectra containing atomic and ionic emission lines as well as molecular emission bands. In the present work, the molecular bands are analyzed to obtain spectroscopic information about the plasma state in an effort to quantify the content of different elements in the polymers. Polyethylene (PE) and a rubber material from tire production are investigated employing 157 nm F2 laser and 532 nm Nd:YAG laser ablation in nitrogen and argon gas background or in air. The optical detection reaches from ultraviolet (UV) over the visible (VIS) to the near infrared (NIR) spectral range. In the UV/VIS range, intense molecular emissions, C2 Swan and CN violet bands, are measured with an Echelle spectrometer equipped with an intensified CCD camera. The measured molecular emission spectra can be fitted by vibrational-rotational transitions by open access programs and data sets with good agreement between measured and fitted spectra. The fits allow determining vibrational-rotational temperatures. A comparison to electronic temperatures Te derived earlier from atomic carbon vacuum-UV (VUV) emission lines show differences, which can be related to different locations of the atomic and molecular species in the expanding plasma plume. In the NIR spectral region, we also observe the CN red bands with a conventional CDD Czerny Turner spectrometer. The emission of the three strong atomic sulfur lines between 920 and 925 nm is overlapped by these bands. Fitting of the CN red bands allows a separation of both spectral contributions. This makes a quantitative evaluation of sulfur contents in the start material in the order of 1 wt% feasible.

  8. Galactic Outflows in Absorption and Emission: Near-UV Spectroscopy of Galaxies at 1

    CERN Document Server

    Erb, Dawn K; Henry, Alaina L; Martin, Crystal L

    2012-01-01

    We study large-scale outflows in a sample of 96 star-forming galaxies at 1spectroscopy of FeII and MgII absorption and emission. The average blueshift of the FeII interstellar absorption lines with respect to the systemic velocity is -85+/-10 km/s at z~1.5, with standard deviation 87 km/s; this is a decrease of a factor of two from the average blueshift measured for far-UV interstellar absorption lines in similarly selected galaxies at z~2. The profiles of the MgII 2796, 2803 lines show much more variety than the FeII profiles, which are always seen in absorption; MgII ranges from strong emission to pure absorption, with emission more common in galaxies with blue UV slopes and at lower stellar masses. Outflow velocities, as traced by the centroids and maximum extent of the absorption lines, increase with increasing stellar mass with 2-3sigma significance, in agreement with previous results. We study fine structure emission from FeII*, finding several lines of evidence in support of t...

  9. Measuring NMHC and NMOG emissions from motor vehicles via FTIR spectroscopy

    Science.gov (United States)

    Gierczak, Christine A.; Kralik, Lora L.; Mauti, Adolfo; Harwell, Amy L.; Maricq, M. Matti

    2017-02-01

    The determination of non-methane organic gases (NMOG) emissions according to United States Environmental Protection Agency (EPA) regulations is currently a multi-step process requiring separate measurement of various emissions components by a number of independent on-line and off-line techniques. The Fourier transform infrared spectroscopy (FTIR) method described in this paper records all required components using a single instrument. It gives data consistent with the regulatory method, greatly simplifies the process, and provides second by second time resolution. Non-methane hydrocarbons (NMHCs) are measured by identifying a group of hydrocarbons, including oxygenated species, that serve as a surrogate for this class, the members of which are dynamically included if they are present in the exhaust above predetermined threshold levels. This yields an FTIR equivalent measure of NMHC that correlates within 5% to the regulatory flame ionization detection (FID) method. NMOG is then determined per regulatory calculation solely from FTIR recorded emissions of NMHC, ethanol, acetaldehyde, and formaldehyde, yielding emission rates that also correlate within 5% with the reference method. Examples are presented to show how the resulting time resolved data benefit aftertreatment development for light duty vehicles.

  10. Emission enhancement using two orthogonal targets in double pulse laser-induced breakdown spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez-Ake, C. [Laboratorio de Fotofisica, Centro de Ciencias Aplicadas y Desarrollo Tecnologico, Universidad Nacional Autonoma de Mexico, Apartado Postal 70-186, Mexico D.F., C.P. 04510 (Mexico)], E-mail: citlali.sanchez@ccadet.unam.mx; Bolanos, Marduk [Laboratorio de Fotofisica, Centro de Ciencias Aplicadas y Desarrollo Tecnologico, Universidad Nacional Autonoma de Mexico, Apartado Postal 70-186, Mexico D.F., C.P. 04510 (Mexico); Ramirez, C.Z. [Colegio de Ciencias y Humanidades Plantel Sur, Universidad Nacional Autonoma de Mexico (Mexico)

    2009-09-15

    The enhancement of emission intensity resulting from the interaction between two laser-induced plasmas on two orthogonal targets was investigated using double pulse laser-induced breakdown spectroscopy (LIBS) at 0.7 Pa, by means of time-resolved spectroscopy and fast photography. The results showed that the interaction between both plasmas improved carbon emission intensity in comparison to a single laser-induced plasma. For all the carbon lines of interest 477.2 nm (CI), 426.7 nm (CII), and 473.4 nm (C{sub 2} Swan band head), the intensity enhancement showed a maximum at a delay between lasers in the range from 2 to 5 {mu}s; moreover it increased with the fluence of the first laser. On the other hand, in the case of C{sub 2} the intensity enhancement reached a maximum at 5 mm from the target; however it decreased with increasing fluence of the second laser. The largest intensity enhancement found was twofold for atomic species and sixfold for molecular species.

  11. Chemical Modification of Graphene Oxide by Nitrogenation: An X-ray Absorption and Emission Spectroscopy Study

    Science.gov (United States)

    Chuang, Cheng-Hao; Ray, Sekhar C.; Mazumder, Debarati; Sharma, Surbhi; Ganguly, Abhijit; Papakonstantinou, Pagona; Chiou, Jau-Wern; Tsai, Huang-Ming; Shiu, Hung-Wei; Chen, Chia-Hao; Lin, Hong-Ji; Guo, Jinghua; Pong, Way-Faung

    2017-02-01

    Nitrogen-doped graphene oxides (GO:Nx) were synthesized by a partial reduction of graphene oxide (GO) using urea [CO(NH2)2]. Their electronic/bonding structures were investigated using X-ray absorption near-edge structure (XANES), valence-band photoemission spectroscopy (VB-PES), X-ray emission spectroscopy (XES) and resonant inelastic X-ray scattering (RIXS). During GO:Nx synthesis, different nitrogen-bonding species, such as pyrrolic/graphitic-nitrogen, were formed by replacing of oxygen-containing functional groups. At lower N-content (2.7 at%), pyrrolic-N, owing to surface and subsurface diffusion of C, N and NH is deduced from various X-ray spectroscopies. In contrast, at higher N-content (5.0 at%) graphitic nitrogen was formed in which each N-atom trigonally bonds to three distinct sp2-hybridized carbons with substitution of the N-atoms for C atoms in the graphite layer. Upon nitrogen substitution, the total density of state close to Fermi level is increased to raise the valence-band maximum, as revealed by VB-PES spectra, indicating an electron donation from nitrogen, molecular bonding C/N/O coordination or/and lattice structure reorganization in GO:Nx. The well-ordered chemical environments induced by nitrogen dopant are revealed by XANES and RIXS measurements.

  12. Chemical Modification of Graphene Oxide by Nitrogenation: An X-ray Absorption and Emission Spectroscopy Study

    Science.gov (United States)

    Chuang, Cheng-Hao; Ray, Sekhar C.; Mazumder, Debarati; Sharma, Surbhi; Ganguly, Abhijit; Papakonstantinou, Pagona; Chiou, Jau-Wern; Tsai, Huang-Ming; Shiu, Hung-Wei; Chen, Chia-Hao; Lin, Hong-Ji; Guo, Jinghua; Pong, Way-Faung

    2017-01-01

    Nitrogen-doped graphene oxides (GO:Nx) were synthesized by a partial reduction of graphene oxide (GO) using urea [CO(NH2)2]. Their electronic/bonding structures were investigated using X-ray absorption near-edge structure (XANES), valence-band photoemission spectroscopy (VB-PES), X-ray emission spectroscopy (XES) and resonant inelastic X-ray scattering (RIXS). During GO:Nx synthesis, different nitrogen-bonding species, such as pyrrolic/graphitic-nitrogen, were formed by replacing of oxygen-containing functional groups. At lower N-content (2.7 at%), pyrrolic-N, owing to surface and subsurface diffusion of C, N and NH is deduced from various X-ray spectroscopies. In contrast, at higher N-content (5.0 at%) graphitic nitrogen was formed in which each N-atom trigonally bonds to three distinct sp2-hybridized carbons with substitution of the N-atoms for C atoms in the graphite layer. Upon nitrogen substitution, the total density of state close to Fermi level is increased to raise the valence-band maximum, as revealed by VB-PES spectra, indicating an electron donation from nitrogen, molecular bonding C/N/O coordination or/and lattice structure reorganization in GO:Nx. The well-ordered chemical environments induced by nitrogen dopant are revealed by XANES and RIXS measurements. PMID:28186190

  13. A system for endoscopic mechanically scanned localized proton MR and light-induced fluorescence emission spectroscopies

    Science.gov (United States)

    Sonmez, Ahmet E.; Webb, Andrew G.; Spees, William M.; Ozcan, Alpay; Tsekos, Nikolaos V.

    2012-09-01

    Molecular and near-cellular modalities offer new opportunities in assessing living tissue in situ, and multimodality approaches, which offer complementary information, may lead to improved characterization of tissue pathophysiology benefiting diagnosis and focal therapy. However, many such modalities are limited by their low penetration through tissue, which has led to minimally invasive trans-cannula approaches to place the corresponding sensors locally at the area of interest. This work presents a system for performing localized fluorescence emission and proton magnetic resonance (MR) spectroscopies via endoscopic access. The in-house developed side-firing 1.9-mm wide dual-sensor integrates a three-fiber optical sensor for fluorescence emission optical spectroscopy and a 1-mm circular radiofrequency (RF) coil for localized MR proton spectroscopy. An MR-compatible manipulator was developed for carrying and mechanically translating the dual-sensor along a linear access channel. The hardware and software control of the system allows reconfigurable synchronization of the manipulator-assisted translation of the sensor, and MR and optical data collection. The manipulator serves as the mechanical link for the three modalities and MR images, MR spectra and optical spectra are inherently co-registered to the MR scanner coordinate system. These spectra were then used to generate spatio-spectral maps of the fluorophores and proton MR-signal sources in three-compartment phantoms with optically- and MR-visible, and distinguishable, materials. These data demonstrate a good spatial match between MR images, MR spectra and optical spectra along the scanned path. In addition to basic research, such a system may have clinical applications for assessing and characterizing cancer in situ, as well as guiding focal therapies.

  14. Glow discharge optical emission spectroscopy: a complementary technique to analyze thin electrodeposited polyaniline films

    Energy Technology Data Exchange (ETDEWEB)

    Moutarlier, V. [Institut UTINAM, CNRS-UMR 6213, Université de Franche-Comté, 16 route de Gray, 25030 Besançon (France); Lakard, S., E-mail: sophie.lakard@univ-fcomte.fr [Institut UTINAM, CNRS-UMR 6213, Université de Franche-Comté, 16 route de Gray, 25030 Besançon (France); Patois, T. [Institute of Condensed Matter and Nanosciences, Université Catholique de Louvain, Croix du Sud, 1/4, 1348 Louvain-la-Neuve (Belgium); Lakard, B. [Institut UTINAM, CNRS-UMR 6213, Université de Franche-Comté, 16 route de Gray, 25030 Besançon (France)

    2014-01-01

    Glow Discharge Optical Emission Spectroscopy (GDOES) has been developed to perform depth profiles of thick metallic films, in tens of microns range. GDOES spectroscopy can also be used to analyze thin organic polymer films since this technique has a great potential thanks to its high depth resolution, multi-element capability, sensitivity, and adaptability to solids or films and to conducting or non-conducting samples. In particular thin electrodeposited conducting polymer films remain an unexplored field of investigation for GDOES technique. However GDOES was used in this work to analyze electrodeposited polyaniline films, in addition to other techniques such as profilometry, electron microscopy and X-ray diffraction (XRD). More precisely polyaniline thin films were electrodeposited from HCl solutions and the presence of an anilinium chloride excess at the top surface of the polymer film was demonstrated using GDOES and XRD. Rinsing of these films with water led to the removal of this excess and to the partial dedoping of the polymer film due to the porous structure of polymer films. Polyaniline thin films were also electrodeposited from H{sub 2}SO{sub 4} solutions and an anilinium hydrogen sulfate was similarly observed at the top surface of the polymer. This excess was removed by rinsing, contrary to hydrogen sulfate anions incorporated into the polymer film during the electrochemical polymerization that were not completely expulsed from the polyaniline films as proved using GDOES. - Highlights: • Polyaniline films were electrodeposited from HCl and H{sub 2}SO{sub 4} solutions • Polymer films were analyzed by Glow Discharge Optical Emission Spectroscopy (GDOES) • The incorporation of anions in the films was proved using GDOES depth profiles • The crystalline structure of polyaniline films was modified by water rinsing.

  15. Optical emission enhancement in laser-induced breakdown spectroscopy using micro-torches

    Science.gov (United States)

    Liu, L.; Huang, X.; Li, S.; Lu, Yao; Chen, K.; Lu, Y. F.

    2016-03-01

    A cost effective method for optical emission enhancement in laser-induced breakdown spectroscopy (LIBS) has been proposed in this research. The pulsed Nd:YAG laser with a wavelength of 532 nm was used for sample ablation and plasma generation. A cost effective commercial butane micro-torch was put parallel to the sample surface to generate a small flame above the surface. The laser-induced plasma expanded in the flame environment. The time-resolved optical emission intensity and signal-to-noise ratio (SNR) have been observed with and without micro torch. For laser with pulse energy of 20 mJ, the relationship between optical emission intensity and delay time indicates that signal intensities have been greatly enhanced in the initial several microseconds when using micro torch. The time-resolved study of signal-to-noise ratio shows that the maximum SNR occurs at the delay time of 2 μs. The laser energy effects on the enhancements of optical emission intensity and SNR have also been analyzed, which indicates that the enhancement factors are both delay time and laser energy dependent. The maximum enhancement factors for both optical emission intensity and SNR gradually decreases with the laser energy increase. The limits of detection (LODs) for aluminum (Al) and molybdenum (Mo) in steel have been estimated, which shows that the detection sensitivity has been improved by around 4 times. The LODs of Al and Mo have been reduced from 18 to 6 ppm and from 110 to 36 ppm in LIBS, respectively. The method of LIBS by a micro torch has been demonstrated to be a cost effective method for detection sensitivity improvement, especially in the situation of low laser pulse energy.

  16. Emission Spectroscopy and Radiometric Measurements in the NASA Ames IHF Arc Jet Facility

    Science.gov (United States)

    Winter, Michael W.; Raiche, George A.; Prabhu, Dinesh K.

    2012-01-01

    Plasma diagnostic measurement campaigns in the NASA Ames Interaction Heating Facility (IHF) have been conducted over the last several years with a view towards characterizing the flow in the arc jet facility by providing data necessary for modeling and simulation. Optical emission spectroscopy has been used in the plenum and in the free jet of the nozzle. Radiation incident over a probe surface has also been measured using radiometry. Plenum measurements have shown distinct radial profiles of temperature over a range of operating conditions. For cases where large amounts of cold air are added radially to the main arc-heated stream, the temperature profiles are higher by as much as 1500 K than the profiles assumed in flow simulations. Optical measurements perpendicular to the flow direction in the free jet showed significant contributions to the molecule emission through inverse pre-dissociation, thus allowing determination of atom number densities from molecular emission. This has been preliminarily demonstrated with the N2 1st Positive System. Despite the use of older rate coefficients, the resulting atom densities are reasonable and surprisingly close to flow predictions.

  17. Fluorescence excitation-emission matrix spectroscopy of vitiligo skin in vivo (Conference Presentation)

    Science.gov (United States)

    Zhao, Jianhua; Richer, Vincent; Al Jasser, Mohammed; Zandi, Soodabeh; Kollias, Nikiforos; Kalia, Sunil; Zeng, Haishan; Lui, Harvey

    2016-02-01

    Fluorescence signals depend on the intensity of the exciting light, the absorption properties of the constituent molecules, and the efficiency with which the absorbed photons are converted to fluorescence emission. The optical features and appearance of vitiligo have been explained primarily on the basis of reduced epidermal pigmentation, which results in abnormal white patches on the skin. The objective of this study is to explore the fluorescence properties of vitiligo and its adjacent normal skin using fluorescence excitation-emission matrix (EEM) spectroscopy. Thirty five (35) volunteers with vitiligo were acquired using a double-grating spectrofluorometer with excitation and emission wavelengths of 260-450 nm and 300-700 nm respectively. As expected, the most pronounced difference between the spectra obtained from vitiligo lesions compared to normally pigmented skin was that the overall fluorescence was much higher in vitiligo; these differences increased at shorter wavelengths, thus matching the characteristic spectral absorption of epidermal melanin. When comparing the fluorescence spectra from vitiligo to normal skin we detected three distinct spectral bands centered at 280nm, 310nm, and 335nm. The 280nm band may possibly be related to inflammation, whereas the 335 nm band may arise from collagen or keratin cross links. The source of the 310 nm band is uncertain; it is interesting to note its proximity to the 311 nm UV lamps used for vitiligo phototherapy. These differences are accounted for not only by changes in epidermal pigment content, but also by other optically active cutaneous biomolecules.

  18. Emission Spectroscopy as a Probe into Photoinduced Intramolecular Electron Transfer in Polyazine Bridged Ru(II,Rh(III Supramolecular Complexes

    Directory of Open Access Journals (Sweden)

    Karen J. Brewer

    2010-08-01

    Full Text Available Steady-state and time-resolved emission spectroscopy are valuable tools to probe photochemical processes of metal-ligand, coordination complexes. Ru(II polyazine light absorbers are efficient light harvesters absorbing in the UV and visible with emissive 3MLCT excited states known to undergo excited state energy and electron transfer. Changes in emission intensity, energy or band-shape, as well as excited state lifetime, provide insight into excited state dynamics. Photophysical processes such as intramolecular electron transfer between electron donor and electron acceptor sub-units may be investigated using these methods. This review investigates the use of steady-state and time-resolved emission spectroscopy to measure excited state intramolecular electron transfer in polyazine bridged Ru(II,Rh(III supramolecular complexes. Intramolecular electron transfer in these systems provides for conversion of the emissive 3MLCT (metal-to-ligand charge transfer excited state to a non-emissive, but potentially photoreactive, 3MMCT (metal-to-metal charge transfer excited state. The details of the photophysics of Ru(II,Rh(III and Ru(II,Rh(III,Ru(II systems as probed by steady-state and time-resolved emission spectroscopy will be highlighted.

  19. Determination of the emissivity of the tungsten hexa-ethoxide pyrolysis flame using Fourier Transform Infrared (FTIR) spectroscopy

    CSIR Research Space (South Africa)

    Mudau, AE

    2010-09-01

    Full Text Available of the Tungsten Hexa-Ethoxide Pyrolysis Flame using Fourier Transform Infrared (FTIR) Spectroscopy Azwitamisi E Mudau1, Bonex W Mwakikunga2, Neels Brink3, Cornelius J Willers1, Andrew Forbes2, Lerato Shikwambana2, Malcolm Govender2 1Defence, Peace... effects. The later is negligible in the setup used. In this paper we present the emissivity of the flame determined from the transmissivity measured using the FTIR Spectroscopy. 1. Introduction Laser pyrolysis is a versatile non...

  20. Continuous measurements of volcanic gases from Popocatepetl volcano by thermal emission spectroscopy

    Science.gov (United States)

    Taquet, Noemie; Stremme, Wolfgang; Meza, Israel; Grutter, Michel

    2016-04-01

    Passive volcanic gas emissions have been poorly studied despite their impact on the atmospheric chemistry with important consequences on its geochemical cycles and climate change on regional and global scale. Therefore, long-term monitoring of volcanic gas plumes and their composition are of prime importance for climatic models and the estimation of the volcanic contribution to climate change. We present a new measurement and analysis strategy based on remote thermal emission spectroscopy which can provide continuous (day and night) information of the composition of the volcanic plume. In this study we show results from the Popocatepetl volcano in Mexico with measurements performed during the year 2015 from the Altzomoni Atmospheric Observatory (19.12N, -98.65W, 3,985 masl). This site, which forms part of the RUOA (www.ruoa.unam.mx) and NDACC (https://www2.acom.ucar.edu/irwg) networks, is located north of the crater of this active volcano at 12 km distance. Emission spectra were recorded with an FTIR spectrometer (OPAG22, Bruker) at 0.5 cm-1 spectral resolution and processed using the SFIT4 radiative transfer and profile retrieval code, based on the Optimal Estimation method (Rodgers, 1976; 1990; 2000). This newly improved methodology is intercompared to a former retrieval strategy using measurements from 2008 and recent results of the variability of the SiF4/SO2 composition ratio during 2015 is presented. A discussion of how the new measurements improve the understating of the impact of volcanic gas emissions on the atmosphere on global and regional scale is included.

  1. Asphaltene Erosion Process in Air Plasma: Emission Spectroscopy and Surface Analysis for Air-Plasma Reactions

    Institute of Scientific and Technical Information of China (English)

    H. MARTINEZ; O. FLORES; J. C. POVEDA; B. CAMPILLO

    2012-01-01

    Optical emission spectroscopy (OES) was applied for plasma characterization during the erosion of asphaltene substrates. An amount of 100 mg of asphaltene was carefully applied to an electrode and exposed to air-plasma glow discharge at a pressure of 1.0 Torr. The plasma was generated in a stainless steel discharge chamber by an ac generator at a frequency of 60 Hz, output power of 50 W and a gas flow rate of 1.8 L/min. The electron temperature and ion density were estimated to be 2.15±0.11 eV and (1.24±0.05)× 10^16 m^-3, respectively, using a double Langmuir probe. OES was employed to observe the emission from the asphaltene exposed to air plasma. Both molecular band emission from N2, N2+, OH, CH, NH, O2 as well as CN, and atomic light emission from V and Hγ were observed and used to monitor the evolution of asphaltene erosion. The asphaltene erosion was analyzed with the aid of a scanning electron microscope (SEM) equipped with an energy dispersive X-ray (EDX) detector. The EDX analysis showed that the time evolution of elements C, O, S and V were similar and the chemical composition of the exposed asphaltenes remained constant. Particle size evolution was measured, showing a maximum size of 2307 μm after 60 min. This behavior is most likely related to particle agglomeration as a function of time.

  2. Emission enhancement of laser-induced breakdown spectroscopy by localized surface plasmon resonance for analyzing plant nutrients.

    Science.gov (United States)

    Ohta, Takayuki; Ito, Masafumi; Kotani, Takashi; Hattori, Takeaki

    2009-05-01

    We demonstrate the monitoring of plant nutrients in leaves of Citrus unshiu and Rhododendron obtusum using low-energy (laser-induced breakdown spectroscopy. The raw plant leaf was successfully ablated without desiccation before laser irradiation, by applying metallic colloidal particles to the leaf surface. The emission intensity with the metallic particles was larger than that without the particles. This result indicates an improvement of the sensitivity and the detection limit of laser-induced breakdown spectroscopy. The emission enhancement was caused by localized surface plasmon resonance and was dependent on the size and material of metallic particles.

  3. The chemical sensitivity of X-ray spectroscopy: high energy resolution XANES versus X-ray emission spectroscopy of substituted ferrocenes.

    Science.gov (United States)

    Atkins, Andrew J; Bauer, Matthias; Jacob, Christoph R

    2013-06-07

    X-ray spectroscopy at the metal K-edge is an important tool for understanding catalytic processes and provides insight into the geometric and electronic structures of transition metal complexes. In particular, X-ray emission-based methods such as high-energy resolution fluorescence detection (HERFD), X-ray absorption near-edge spectroscopy (XANES) and valence-to-core X-ray emission spectroscopy (V2C-XES) hold the promise of providing increased chemical sensitivity compared to conventional X-ray absorption spectroscopy. Here, we explore the ability of HERFD-XANES and V2C-XES spectroscopy to distinguish substitutions beyond the directly coordinated atoms for the example of ferrocene and selected ferrocene derivatives. The experimental spectra are assigned and interpreted through the use of density functional theory (DFT) calculations. We find that while the pre-edge peaks in the HERFD-XANES spectra are affected by substituents at the cyclopentadienyl ring containing π-bonds [A. J. Atkins, Ch. R. Jacob and M. Bauer, Chem.-Eur. J., 2012, 18, 7021], the V2C-XES spectra are virtually unchanged. The pre-edge in HERFD-XANES probes the weak transition to unoccupied metal d-orbitals, while the V2C-XES spectra are determined by dipole-allowed transitions from occupied ligand orbitals to the 1s core hole. The latter turn out to be less sensitive to changes beyond the first coordination shell.

  4. Development of beam emission spectroscopy for turbulence transport study in Heliotron J

    Energy Technology Data Exchange (ETDEWEB)

    Kobayashi, S., E-mail: kobayashi@iae.kyoto-u.ac.jp; Ohshima, S.; Kado, S.; Nagasaki, K.; Okada, H.; Minami, T.; Yamamoto, S.; Konoshima, S.; Mizuuchi, T. [Institute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011 (Japan); Matsuda, H.; Lu, X. X.; Kokubu, D.; Nakamura, Y.; Ishizawa, A.; Otani, Y. [Graduate School of Energy Science, Kyoto University, Uji, Kyoto 611-0011 (Japan); Ida, K.; Kobayashi, T.; Yoshinuma, M.; Oishi, T.; Kenmochi, N. [National Institute for Fusion Science, Oroshi-cho 322-6, Toki, Gifu 509-5292 (Japan)

    2016-11-15

    This paper describes the development study of the beam emission spectroscopy (BES) for the turbulent transport study in Heliotron J. Modification of the sightlines (10 × 4 for edge and 10 × 2 for edge) enables us to obtain 2-dimensional BES imaging. The cooling effect on the reduction in the electrical noise of avalanche photodiode (APD) assembly has been investigated using a refrigerant cooling system. When the temperature of the APD element has set to be −20 °C, the electrical noise can be reduced more than 50%. The measurement error of the phase difference in the case of low signal level has been tested by two light-emitting diode lamps. The APD cooling has an effect to improve the measurement error at the low signal level of APD.

  5. Temperature Effect on the Optical Emission Intensity in Laser Induced Breakdown Spectroscopy of Super Alloys

    Science.gov (United States)

    Darbani, S. M. R.; Ghezelbash, M.; Majd, A. E.; Soltanolkotabi, M.; Saghafifar, H.

    2014-12-01

    In this paper, the influence of heating and cooling samples on the optical emission spectra and plasma parameters of laser-induced breakdown spectroscopy for Titanium 64, Inconel 718 super alloys, and Aluminum 6061 alloy is investigated. Samples are uniformly heated up to approximately 200°C and cooled down to -78°C by an external heater and liquid nitrogen, respectively. Variations of plasma parameters like electron temperature and electron density with sample temperature are determined by using Boltzmann plot and Stark broadening methods, respectively. Heating the samples improves LIBS signal strength and broadens the width of the spectrum. On the other hand, cooling alloys causes fluctuations in the LIBS signal and decrease it to some extent, and some of the spectral peaks diminish. In addition, our results show that electron temperature and electron density depend on the sample temperature variations.

  6. Development of beam emission spectroscopy for turbulence transport study in Heliotron J

    Science.gov (United States)

    Kobayashi, S.; Ohshima, S.; Matsuda, H.; Lu, X. X.; Kokubu, D.; Ida, K.; Kobayashi, T.; Yoshinuma, M.; Kado, S.; Oishi, T.; Nagasaki, K.; Okada, H.; Minami, T.; Yamamoto, S.; Nakamura, Y.; Ishizawa, A.; Kenmochi, N.; Otani, Y.; Konoshima, S.; Mizuuchi, T.

    2016-11-01

    This paper describes the development study of the beam emission spectroscopy (BES) for the turbulent transport study in Heliotron J. Modification of the sightlines (10 × 4 for edge and 10 × 2 for edge) enables us to obtain 2-dimensional BES imaging. The cooling effect on the reduction in the electrical noise of avalanche photodiode (APD) assembly has been investigated using a refrigerant cooling system. When the temperature of the APD element has set to be -20 °C, the electrical noise can be reduced more than 50%. The measurement error of the phase difference in the case of low signal level has been tested by two light-emitting diode lamps. The APD cooling has an effect to improve the measurement error at the low signal level of APD.

  7. In vivo neurochemistry with emission tomography and magnetic resonance spectroscopy: clinical applications.

    Science.gov (United States)

    Del Sole, Angelo; Gambini, Anna; Falini, Andrea; Lecchi, Michela; Lucignani, Giovanni

    2002-10-01

    The assessment of neurochemical processes in vivo has received much attention in the past decade as techniques such as positron or single photon emission tomography (PET and SPET), and magnetic resonance spectroscopy (MRS) have become more available. With PET and SPET, basic processes, such as blood flow and oxygen or glucose metabolism, can be regionally assessed, along with more specific functions such as the production, release, and reuptake of neurotransmitters and their occupancy of specific receptors. At the same time, MRS can reveal changes in concentration of several hydrogenate compounds in the brain. All these methods have been extensively applied for research in neurology, and some applications have reached the clinical level, namely for the study of degenerative diseases, motor-neuron diseases, movement disorders, cerebrovascular diseases, and epilepsy. This article focuses on the most relevant information that can be obtained with these complementary techniques to help clinicians in the assessment of neurological diseases.

  8. In vivo neurochemistry with emission tomography and magnetic resonance spectroscopy: clinical applications

    Energy Technology Data Exchange (ETDEWEB)

    Sole, Angelo Del [Azienda Ospedaliera San Paolo e Universita di Milano, 20142 Milan (Italy); Gambini, Anna; Falini, Andrea [IRCCS H San Raffaele e Universita Vita e Salute, 20132 Milan (Italy); Lecchi, Michela [Azienda Ospedaliera L. Sacco e Universita di Milano, 20157 Milan (Italy); Lucignani, Giovanni [Azienda Ospedaliera L. Sacco e Universita di Milano, 20157 Milan (Italy); Universita di Milano, Istituto di Scienze Radiologiche, Cattedra di Medicina Nucleare c/o Ospedale L. Sacco, Via G.B. Grassi, 74, 20157 Milan (Italy)

    2002-10-01

    The assessment of neurochemical processes in vivo has received much attention in the past decade as techniques such as positron or single photon emission tomography (PET and SPET), and magnetic resonance spectroscopy (MRS) have become more available. With PET and SPET, basic processes, such as blood flow and oxygen or glucose metabolism, can be regionally assessed, along with more specific functions such as the production, release, and reuptake of neurotransmitters and their occupancy of specific receptors. At the same time, MRS can reveal changes in concentration of several hydrogenate compounds in the brain. All these methods have been extensively applied for research in neurology, and some applications have reached the clinical level, namely for the study of degenerative diseases, motor-neuron diseases, movement disorders, cerebrovascular diseases, and epilepsy. This article focuses on the most relevant information that can be obtained with these complementary techniques to help clinicians in the assessment of neurological diseases. (orig.)

  9. Plasma diagnostics in gas metal arc welding by optical emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Valensi, F; Pellerin, S; Zielinska, S [GREMI, Universite d' Orleans (Site de Bourges)/CNRS, BP 4043, 18028 Bourges cedex (France); Boutaghane, A [Universite des Sciences et de la Technologie Houari Boumediene, Alger (Algeria); Dzierzega, K [Marian Smoluchowski Institute of Physics, Jagellonian University, Krakow (Poland); Pellerin, N [CNRS, UPR3079 CEMHTI, 1D av. de la Recherche Scientifique, 45071 Orleans cedex 2 (France); Briand, F, E-mail: flavien.valensi@laplace.univ-tsle.f, E-mail: stephane.pellerin@univ-orleans.f, E-mail: aboutaghane@yahoo.f, E-mail: krzycho@netmail.if.uj.edu.p, E-mail: sylwia.zielinska@airliquide.co, E-mail: nadia.pellerin@univ-orleans.f, E-mail: francis.briand@airliquide.co [CTAS-Air Liquide Welding, Saint Ouen l' Aumone, 95315 Cergy-Pontoise cedex (France)

    2010-11-03

    The plasma column in a metal inert gas welding process is investigated by optical emission spectroscopy and high-speed imaging. The concentration and repartition of iron vapours are measured and correlated with the plasma and electrode geometric configuration. Plasma temperatures and electron densities are also measured for each studied position in the plasma. The temperatures are calculated using two different methods, allowing validation of the local thermodynamic equilibrium state of the plasma. The results show a maximum temperature of 12 500 K in the upper part of the arc, away from the arc axis. The iron concentration reaches a maximum of 0.3% close to the anode and strongly decreases along both the vertical and radial directions. The plasma thermophysical properties, calculated from this plasma composition, are then discussed regarding the metal transfer mode.

  10. SPATIALLY RESOLVED HST GRISM SPECTROSCOPY OF A LENSED EMISSION LINE GALAXY AT z {approx} 1

    Energy Technology Data Exchange (ETDEWEB)

    Frye, Brenda L. [Steward Observatory, Department of Astronomy, University of Arizona, 933 North Cherry Avenue, Tucson, AZ 85721 (United States); Hurley, Mairead [School of Physical Sciences, Dublin City University, Glasnevin, Dublin 9 (Ireland); Bowen, David V. [Department of Astrophysical Sciences, Peyton Hall, Princeton University, Princeton, NJ 08540 (United States); Meurer, Gerhardt [International Centre for Radio Astronomy Research, The University of Western Australia M468, 35 Stirling Highway, Crawley, WA 6009 (Australia); Sharon, Keren [Department of Astronomy and Astrophysics, The University of Chicago, Chicago, IL 60637 (United States); Straughn, Amber [Astrophysics Science Division, Goddard Space Flight Center, Code 665, Greenbelt, MD 20771 (United States); Coe, Dan [Space Telescope Science Institute, 3700 San Martin Drive, Baltimore, MD 21218 (United States); Broadhurst, Tom [Ikerbasque, Basque Foundation for Science, E-48011 Bilbao (Spain); Guhathakurta, Puragra, E-mail: bfrye@as.arizona.edu [UCO/Lick Observatory, Department of Astronomy and Astrophysics, University of California, Santa Cruz, CA 95064 (United States)

    2012-07-20

    We take advantage of gravitational lensing amplification by A1689 (z 0.187) to undertake the first space-based census of emission line galaxies (ELGs) in the field of a massive lensing cluster. Forty-three ELGs are identified to a flux of i{sub 775} = 27.3 via slitless grism spectroscopy. One ELG (at z = 0.7895) is very bright owing to lensing magnification by a factor of Almost-Equal-To 4.5. Several Balmer emission lines (ELs) detected from ground-based follow-up spectroscopy signal the onset of a major starburst for this low-mass galaxy (M{sub *} Almost-Equal-To 2 Multiplication-Sign 10{sup 9} M{sub Sun }) with a high specific star formation rate ( Almost-Equal-To 20 Gyr{sup -1}). From the blue ELs we measure a gas-phase oxygen abundance consistent with solar (12+log(O/H) = 8.8 {+-} 0.2). We break the continuous line-emitting region of this giant arc into seven {approx}1 kpc bins (intrinsic size) and measure a variety of metallicity-dependent line ratios. A weak trend of increasing metal fraction is seen toward the dynamical center of the galaxy. Interestingly, the metal line ratios in a region offset from the center by {approx}1 kpc have a placement on the blue H II region excitation diagram with f ([O III])/f (H{beta}) and f ([Ne III])/f (H{beta}) that can be fitted by an active galactic nucleus (AGN). This asymmetrical AGN-like behavior is interpreted as a product of shocks in the direction of the galaxy's extended tail, possibly instigated by a recent galaxy interaction.

  11. Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Hellman, Hal

    1968-01-01

    This booklet discusses spectroscopy, the study of absorption of radiation by matter, including X-ray, gamma-ray, microwave, mass spectroscopy, as well as others. Spectroscopy has produced more fundamental information to the study of the detailed structure of matter than any other tools.

  12. Combined hydrogen and lithium beam emission spectroscopy observation system for Korea Superconducting Tokamak Advanced Research

    Energy Technology Data Exchange (ETDEWEB)

    Lampert, M. [Wigner RCP, Euratom Association-HAS, Budapest (Hungary); BME NTI, Budapest (Hungary); Anda, G.; Réfy, D.; Zoletnik, S. [Wigner RCP, Euratom Association-HAS, Budapest (Hungary); Czopf, A.; Erdei, G. [Department of Atomic Physics, BME IOP, Budapest (Hungary); Guszejnov, D.; Kovácsik, Á.; Pokol, G. I. [BME NTI, Budapest (Hungary); Nam, Y. U. [National Fusion Research Institute, Daejeon (Korea, Republic of)

    2015-07-15

    A novel beam emission spectroscopy observation system was designed, built, and installed onto the Korea Superconducting Tokamak Advanced Research tokamak. The system is designed in a way to be capable of measuring beam emission either from a heating deuterium or from a diagnostic lithium beam. The two beams have somewhat complementary capabilities: edge density profile and turbulence measurement with the lithium beam and two dimensional turbulence measurement with the heating beam. Two detectors can be used in parallel: a CMOS camera provides overview of the scene and lithium beam light intensity distribution at maximum few hundred Hz frame rate, while a 4 × 16 pixel avalanche photo-diode (APD) camera gives 500 kHz bandwidth data from a 4 cm × 16 cm region. The optics use direct imaging through lenses and mirrors from the observation window to the detectors, thus avoid the use of costly and inflexible fiber guides. Remotely controlled mechanisms allow adjustment of the APD camera’s measurement location on a shot-to-shot basis, while temperature stabilized filter holders provide selection of either the Doppler shifted deuterium alpha or lithium resonance line. The capabilities of the system are illustrated by measurements of basic plasma turbulence properties.

  13. Updated Spitzer emission spectroscopy of bright transiting hot Jupiter HD 189733b

    Energy Technology Data Exchange (ETDEWEB)

    Todorov, Kamen O. [Department of Astronomy and Astrophysics, The Pennsylvania State University, University Park, PA 16802 (United States); Deming, Drake [Department of Astronomy, University of Maryland at College Park, College Park, MD 20742 (United States); Burrows, Adam [Department of Astrophysical Sciences, Princeton University, Princeton, NJ 08544 (United States); Grillmair, Carl J., E-mail: todorovk@phys.ethz.ch [Spitzer Science Center, California Institute of Technology, Mail Stop 220-6, Pasadena, CA 91125 (United States)

    2014-12-01

    We analyze all existing secondary eclipse time series spectroscopy of hot Jupiter HD 189733b acquired with the now defunct Spitzer/Infrared Spectrograph (IRS) instrument. We describe the novel approaches we develop to remove the systematic effects and extract accurate secondary eclipse depths as a function of wavelength in order to construct the emission spectrum of the exoplanet. We compare our results with a previous study by Grillmair et al. that did not examine all data sets available to us. We are able to confirm the detection of a water feature near 6 μm claimed by Grillmair et al. We compare the planetary emission spectrum to three model families—based on isothermal atmosphere, gray atmosphere, and two realizations of the complex radiative transfer model by Burrows et al., adopted in Grillmair et al.'s study. While we are able to reject the simple isothermal and gray models based on the data at the 97% level just from the IRS data, these rejections hinge on eclipses measured within a relatively narrow wavelength range, between 5.5 and 7 μm. This underscores the need for observational studies with broad wavelength coverage and high spectral resolution, in order to obtain robust information on exoplanet atmospheres.

  14. LZIFU: an emission-line fitting toolkit for integral field spectroscopy data

    Science.gov (United States)

    Ho, I.-Ting; Medling, Anne M.; Groves, Brent; Rich, Jeffrey A.; Rupke, David S. N.; Hampton, Elise; Kewley, Lisa J.; Bland-Hawthorn, Joss; Croom, Scott M.; Richards, Samuel; Schaefer, Adam L.; Sharp, Rob; Sweet, Sarah M.

    2016-09-01

    We present lzifu (LaZy-IFU), an idl toolkit for fitting multiple emission lines simultaneously in integral field spectroscopy (IFS) data. lzifu is useful for the investigation of the dynamical, physical and chemical properties of gas in galaxies. lzifu has already been applied to many world-class IFS instruments and large IFS surveys, including the Wide Field Spectrograph, the new Multi Unit Spectroscopic Explorer (MUSE), the Calar Alto Legacy Integral Field Area (CALIFA) survey, the Sydney-Australian-astronomical-observatory Multi-object Integral-field spectrograph (SAMI) Galaxy Survey. Here we describe in detail the structure of the toolkit, and how the line fluxes and flux uncertainties are determined, including the possibility of having multiple distinct kinematic components. We quantify the performance of lzifu, demonstrating its accuracy and robustness. We also show examples of applying lzifu to CALIFA and SAMI data to construct emission line and kinematic maps, and investigate complex, skewed line profiles presented in IFS data. The code is made available to the astronomy community through github. lzifu will be further developed over time to other IFS instruments, and to provide even more accurate line and uncertainty estimates.

  15. Spectroscopy

    CERN Document Server

    Walker, S

    1976-01-01

    The three volumes of Spectroscopy constitute the one comprehensive text available on the principles, practice and applications of spectroscopy. By giving full accounts of those spectroscopic techniques only recently introduced into student courses - such as Mössbauer spectroscopy and photoelectron spectroscopy - in addition to those techniques long recognised as being essential in chemistry teaching - sucha as e.s.r. and infrared spectroscopy - the book caters for the complete requirements of undergraduate students and at the same time provides a sound introduction to special topics for graduate students.

  16. Metastable argon atom density in complex argon/acetylene plasmas determined by means of optical absorption and emission spectroscopy

    Science.gov (United States)

    Sushkov, Vladimir; Herrendorf, Ann-Pierra; Hippler, Rainer

    2016-10-01

    Optical emission and absorption spectroscopy has been utilized to investigate the instability of acetylene-containing dusty plasmas induced by growing nano-particles. The density of Ar(1s5) metastable atoms was derived by two methods: tunable diode laser absorption spectroscopy and with the help of the branching ratio method of emitted spectral lines. Results of the two techniques agree well with each other. The density of Ar(1s3) metastable atoms was also measured by means of optical emission spectroscopy. The observed growth instability leads to pronounced temporal variations of the metastable and other excited state densities. An analysis of optical line ratios provides evidence for a depletion of free electrons during the growth cycle but no indication for electron temperature variations.

  17. X-ray emission spectroscopy study of the Verwey transition in Fe sub 3 O sub 4

    CERN Document Server

    Moewes, A; Finkelstein, L D; Galakhov, A V; Gota, S; Gautier-Soyer, M; Rueff, J P; Hague, C F

    2003-01-01

    The temperature-dependent Verwey transition in a 500 A (111) thin film of Fe sub 3 O sub 4 (magnetite) has been studied using soft-x-ray emission spectroscopy at room temperature and below the transition temperature T sub V. The Fe L sub 2 sub , sub 3 x-ray emission spectra show an increase in the intensity of the L sub 2 emission relative to the L sub 3 emission below T sub V. This is independent of the excitation energy and is attributed to a metal-insulator transition across T sub V. Comparison of the Fe L sub 3 emission and O K alpha spectra with LDA band structure calculations supports the suggestion of charge ordering in Fe sub 3 O sub 4 at low temperature.

  18. Atom-specific look at the surface chemical bond using x-ray emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Nilsson, A.; Wassdahl, N.; Weinelt, M. [Uppsala Univ. (Sweden)] [and others

    1997-04-01

    CO and N{sub 2} adsorbed on the late transition metals have become prototype systems regarding the general understanding of molecular adsorption. It is in general assumed that the bonding of molecules to transition metals can be explained in terms of the interaction of the frontier HOMO and LUMO molecular orbitals with the d-orbitals. In such a picture the other molecular orbitals should remain essentially the same as in the free molecule. For the adsorption of the isoelectronic molecules CO and N{sub 2} this has led to the so called Blyholder model i.e., a synergetic {sigma} (HOMO) donor and {pi} (LUMO) backdonation bond. The authors results at the ALS show that such a picture is oversimplified. The direct observation and identification of the states related to the surface chemical bond is an experimental challenge. For noble and transition metal surfaces, the adsorption induced states overlap with the metal d valence band. Their signature is therefore often obscured by bulk substrate states. This complication has made it difficult for techniques such as photoemission and inverse photoemission to provide reliable information on the energy of chemisorption induced states and has left questions unanswered regarding the validity of the frontier orbitals concept. Here the authors show how x-ray emission spectroscopy (XES), in spite of its inherent bulk sensitivity, can be used to investigate adsorbed molecules. Due to the localization of the core-excited intermediate state, XE spectroscopy allows an atomic specific separation of the valence electronic states. Thus the molecular contributions to the surface measurements make it possible to determine the symmetry of the molecular states, i.e., the separation of {pi} and {sigma} type states. In all the authors can obtain an atomic view of the electronic states involved in the formation of the chemical bond to the surface.

  19. Terahertz Desorption Emission Spectroscopy (THz DES) - ‘ALMA in the Lab’

    Science.gov (United States)

    Emile Auriacombe, Olivier Bruno Jacques; Fraser, Helen; Ellison, Brian; Ioppolo, Sergio; Rea, Simon

    2016-06-01

    ALMA is revolutionising our scope to identify and locate molecules that have been desorbed from ices, particularly complex organic molecules (COMS), which provide a vital link between interstellar and prebiotic chemistry. Explaining the existence of these molecules in star-forming regions relies on an empirical understanding of the chemistry that underpins their formation:- do COMS form predominantly in the solid-phase and then desorb to the gas phase, or do only “smaller” species, radials or ions desorb and then undergo gas-phase chemical reactions to generate larger COMS?-are the rotational state populations in COMS only attributable to equilibrium chemistry, or could their formation mechanisms and desorption processes affect the rotational state occupancy of these molecules, thereby directly tying certain species to solid-state origins?We have developed a novel laboratory method - THz Desorption Emission Spectroscopy (THz-DES) that combines “traditional” laboratory astrophysics high-vacuum ice experiments with a sensitive high-spectral-resolution terahertz total-power heterodyne radiometer 1,2, partially mirroring the spectral range of ALMA band 7 (275- 373 GHz). Ices are grown in situ on a cold-plate, situated in a vacuum cell, then (thermally) desorbed. The sub-mm emission spectra of the resultant gas-phase molecules are detected as a function of time, temperature, or distance from the surface. Our first THz DES results will be shown for pure and binary ice systems including H2O, N2O and CH3OH. They show good correlation with established methods e.g. TPD, with the advantage of exploiting the molecular spectroscopy to unravel surface dynamics, state-occupancy, and unequivocal molecular identification, as well as concurrently measuring desorption barriers and molecular yields. We will extend our technique to a broader frequency range, enabling us to detect radical and ion desorption, to differentiate between A and E populations of CH3OH or ortho

  20. Unreported Emission Lines of Rb, Ce, La, Sr, Y, Zr, Pb and Se Detected Using Laser-Induced Breakdown Spectroscopy

    Science.gov (United States)

    Lepore, K. H.; Mackie, J.; Dyar, M. D.; Fassett, C. I.

    2017-01-01

    Information on emission lines for major and minor elements is readily available from the National Institute of Standards and Technology (NIST) as part of the Atomic Spectra Database. However, tabulated emission lines are scarce for some minor elements and the wavelength ranges presented on the NIST database are limited to those included in existing studies. Previous work concerning minor element calibration curves measured using laser-induced break-down spectroscopy found evidence of Zn emission lines that were not documented on the NIST database. In this study, rock powders were doped with Rb, Ce, La, Sr, Y, Zr, Pb and Se in concentrations ranging from 10 percent to 10 parts per million. The difference between normalized spectra collected on samples containing 10 percent dopant and those containing only 10 parts per million were used to identify all emission lines that can be detected using LIBS (Laser-Induced Breakdown Spectroscopy) in a ChemCam-like configuration at the Mount Holyoke College LIBS facility. These emission spectra provide evidence of many previously undocumented emission lines for the elements measured here.

  1. Prediction of methane emission from lactating dairy cows using milk fatty acids and mid-infrared spectroscopy.

    Science.gov (United States)

    van Gastelen, Sanne; Dijkstra, Jan

    2016-09-01

    Enteric methane (CH4 ) production is among the main targets of greenhouse gas mitigation practices for the dairy industry. A simple, robust and inexpensive measurement technique applicable on a large scale to estimate CH4 emission from dairy cattle would therefore be valuable. Milk fatty acids (MFA) are related to CH4 production because of the common biochemical pathway between CH4 and fatty acids in the rumen. A summary of studies that investigated the predictive power of MFA composition for CH4 emission indicated good potential, with predictive power ranging between 47% and 95%. Until recently, gas chromatography (GC) was the principal method used to determine the MFA profile, but GC is unsuitable for routine analysis. This has led to the application of mid-infrared (MIR) spectroscopy. The major advantages of using MIR spectroscopy to predict CH4 emission include its simplicity and potential practical application at large scale. Disadvantages include the inability to predict important MFA for CH4 prediction, and the moderate predictive power for CH4 emission. It may not be sufficient to predict CH4 emission based on MIR alone. Integration with other factors, like feed intake, nutrient composition of the feed, parity, and lactation stage may improve the prediction of CH4 emission using MIR spectra. © 2016 Society of Chemical Industry.

  2. DETECTION OF REST-FRAME OPTICAL LINES FROM X-SHOOTER SPECTROSCOPY OF WEAK EMISSION-LINE QUASARS

    Energy Technology Data Exchange (ETDEWEB)

    Plotkin, Richard M.; Gallo, Elena [Department of Astronomy, University of Michigan, 1085 South University Avenue, Ann Arbor, MI 48109 (United States); Shemmer, Ohad [Department of Physics, University of North Texas, Denton, TX 76203 (United States); Trakhtenbrot, Benny [Institute for Astronomy, Department of Physics, ETH Zurich, Wolfgang-Pauli-Strasse 27, CH-8093 Zurich (Switzerland); Anderson, Scott F. [Department of Astronomy, University of Washington, Box 351580, Seattle, WA 98195 (United States); Brandt, W. N.; Luo, Bin; Schneider, Donald P. [Department of Astronomy and Astrophysics, 525 Davey Lab, The Pennsylvania State University, University Park, PA 16802 (United States); Fan, Xiaohui [Steward Observatory, University of Arizona, 933 North Cherry Avenue, Tucson, AZ 85721 (United States); Lira, Paulina [Departamento de Astronomia, Universidad de Chile, Camino del Observatorio 1515, Santiago (Chile); Richards, Gordon T. [Department of Physics, Drexel University, 3141 Chestnut Street, Philadelphia, PA 19104 (United States); Strauss, Michael A. [Department of Astrophysical Sciences, Princeton University, Princeton, NJ 08544 (United States); Wu, Jianfeng, E-mail: rplotkin@umich.edu [Harvard-Smithsonian Center for Astrophysics, MS 6, 60 Garden Street Cambridge, MA 02138 (United States)

    2015-06-01

    Over the past 15 yr, examples of exotic radio-quiet quasars with intrinsically weak or absent broad emission line regions (BELRs) have emerged from large-scale spectroscopic sky surveys. Here, we present spectroscopy of seven such weak emission line quasars (WLQs) at moderate redshifts (z = 1.4–1.7) using the X-shooter spectrograph, which provides simultaneous optical and near-infrared spectroscopy covering the rest-frame ultraviolet (UV) through optical. These new observations effectively double the number of WLQs with spectroscopy in the optical rest-frame, and they allow us to compare the strengths of (weak) high-ionization emission lines (e.g., C iv) to low-ionization lines (e.g., Mg ii, Hβ, Hα) in individual objects. We detect broad Hβ and Hα emission in all objects, and these lines are generally toward the weaker end of the distribution expected for typical quasars (e.g., Hβ has rest-frame equivalent widths ranging from 15–40 Å). However, these low-ionization lines are not exceptionally weak, as is the case for high-ionization lines in WLQs. The X-shooter spectra also display relatively strong optical Fe ii emission, Hβ FWHM ≲ 4000 km s{sup −1}, and significant C iv blueshifts (≈1000–5500 km s{sup −1}) relative to the systemic redshift; two spectra also show elevated UV Fe ii emission, and an outflowing component to their (weak) Mg ii emission lines. These properties suggest that WLQs are exotic versions of “wind-dominated” quasars. Their BELRs either have unusual high-ionization components, or their BELRs are in an atypical photoionization state because of an unusually soft continuum.

  3. Development of a Reference Database for Particle-Induced Gamma-ray Emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Dimitriou, P., E-mail: P.Dimitriou@iaea.org [International Atomic Energy Agency, Wagramerstrasse 5, A-1400 Vienna (Austria); Becker, H.-W. [Ruhr Universität Bochum, Gebäude NT05/130, Postfach 102148, Bochum 44721 (Germany); Bogdanović-Radović, I. [Department of Experimental Physics, Institute Rudjer Boskovic, Bijenicka Cesta 54, 10000 Zagreb (Croatia); Chiari, M. [Istituto Nazionale di Fisica Nucleare, Via Sansone 1, Sesto Fiorentino, 50019 Firenze (Italy); Goncharov, A. [Kharkov Institute of Physics and Technology, National Science Center, Akademicheskaya Str.1, Kharkov 61108 (Ukraine); Jesus, A.P. [Departamento de Física, Faculdade de Ciências e Tecnologia da Universidade Nova de Lisboa (Portugal); Kakuee, O. [Nuclear Science and Technology Research Institute, End of North Karegar Ave., PO Box 14395-836, Tehran (Iran, Islamic Republic of); Kiss, A.Z. [Institute of Nuclear Research (ATOMKI), Bem ter 18/c, PO Box 51, 4001 Debrecen (Hungary); Lagoyannis, A. [National Center of Scientific Research “Demokritos”, Agia Paraskevi, P.O. Box 60228, 15310 Athens (Greece); Räisänen, J. [Division of Materials Physics, Department of Physics, University of Helsinki, PO Box 43, 00014 University of Helsinki (Finland); Strivay, D. [Institut de Physique Nucleaire, Atomique et de Spectroscopie, Universite de Liège, Sart Tilman, B15 4000 Liège (Belgium); Zucchiatti, A. [Centro de Micro Análisis de Materiales, Universidad Autónoma de Madrid, Faraday 3, Madrid 28049 (Spain)

    2016-03-15

    Particle-Induced Gamma-ray Emission (PIGE) is a powerful analytical technique that exploits the interactions of rapid charged particles with nuclei located near a sample surface to determine the composition and structure of the surface regions of solids by measurement of characteristic prompt γ rays. The potential for depth profiling of this technique has long been recognized, however, the implementation has been limited owing to insufficient knowledge of the physical data and lack of suitable user-friendly computer codes for the applications. Although a considerable body of published data exists in the nuclear physics literature for nuclear reaction cross sections with γ rays in the exit channel, there is no up-to-date, comprehensive compilation specifically dedicated to IBA applications. A number of PIGE cross-section data had already been uploaded to the Ion Beam Analysis Nuclear Data Library (IBANDL) ( (http://www-nds.iaea.org/ibandl)) by members of the IBA community by 2011, however a preliminary survey of this body of unevaluated experimental data has revealed numerous discrepancies beyond the uncertainty limits reported by the authors. Using the resources and coordination provided by the IAEA, a concerted effort to improve the situation was made within the Coordinated Research Project on the Development of a Reference Database for PIGE spectroscopy, from 2011 to 2015. The aim of the CRP was to create a data library for Ion Beam Analysis that contains reliable and usable data on charged particle γ-ray emission cross sections that would be made freely available to the user community. As the CRP has reached its completion, we shall present its main achievements, including the results of nuclear cross-section evaluations and the development of a computer code that will become available to the public allowing for the implementation of a standardless PIGE technique.

  4. Determination of total tin in canned food using inductively coupled plasma atomic emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Perring, Loic; Basic-Dvorzak, Marija [Department of Quality and Safety Assurance, Nestle Research Centre, P.O. Box 44, Vers chez-les-Blanc, 1000, Lausanne (Switzerland)

    2002-09-01

    Tin is considered to be a priority contaminant by the Codex Alimentarius Commission. Tin can enter foods either from natural sources, environmental pollution, packaging material or pesticides. Higher concentrations are found in processed food and canned foods. Dissolution of the tinplate depends on the of food matrix, acidity, presence of oxidising reagents (anthocyanin, nitrate, iron and copper) presence of air (oxygen) in the headspace, time and storage temperature. To reduce corrosion and dissolution of tin, nowadays cans are usually lacquered, which gives a marked reduction of tin migration into the food product. Due to the lack of modern validated published methods for food products, an ICP-AES (Inductively coupled plasma-atomic emission spectroscopy) method has been developed and evaluated. This technique is available in many laboratories in the food industry and is more sensitive than atomic absorption. Conditions of sample preparation and spectroscopic parameters for tin measurement by axial ICP-AES were investigated for their ruggedness. Two methods of preparation involving high-pressure ashing or microwave digestion in volumetric flasks were evaluated. They gave complete recovery of tin with similar accuracy and precision. Recoveries of tin from spiked products with two levels of tin were in the range 99{+-}5%. Robust relative repeatabilities and intermediate reproducibilities were <5% for different food matrices containing >30 mg/kg of tin. Internal standard correction (indium or strontium) did not improve the method performance. Three emission lines for tin were tested (189.927, 283.998 and 235.485 nm) but only 189.927 nm was found to be robust enough with respect to interferences, especially at low tin concentrations. The LOQ (limit of quantification) was around 0.8 mg/kg at 189.927 nm. A survey of tin content in a range of canned foods is given. (orig.)

  5. High resolution X-ray emission spectroscopy: An advanced tool for actinide research

    Energy Technology Data Exchange (ETDEWEB)

    Vitova, T; Brendebach, B; Dardenne, K; Denecke, M A; Lebid, A; Loeble, M; Rothe, J; Batuk, O N; Geckeis, H [Karlsruhe Institut fuer Technologie (KIT), Institut fuer Nukleare Entsorgung (INE), PO Box 3640, D-76021 Karlsruhe (Germany); Hormes, J; Liu, D [Physikalisches Institut, Nussallee 12, D-53115 Bonn (Germany); Breher, F, E-mail: tonya.vitova@kit.edu [Karlsruhe Institut fuer Technologie (KIT), Institut fuer Anorganische Chemie, Engesserstr. 15, D-76131 Karlsruhe (Germany)

    2010-03-15

    High resolution X-ray emission spectroscopy (HRXES) is becoming increasingly important for our understanding of electronic and coordination structures. The combination of such information with development of quantum theoretical tools will advance our capability for predicting reactivity and physical behavior especially of 5f elements. HRXES can be used to remove lifetime broadening by registering the partial fluorescence yield emitted by the sample (i.e., recording a windowed signal from the energy dispersed fluorescence emission while varying incident photon energy), thereby yielding highly resolved X-ray absorption fine structure (XAFS) spectra. Such spectra often display resonant features not observed in conventional XAFS. The spectrometer set-up can also be used for a wide range of other experiments, for example, resonant inelastic X-ray scattering (RIXS), where bulk electron configuration information in solids, liquids and gases is obtained. Valence-selective XAFS studies, where the local structure of a selected element's valence state present in a mixture of valence states can be obtained, as well as site-selective XAFS studies, where the coordination structure of a metal bound to selected elements can be differentiated from that of all the other ligating atoms. A HRXES spectrometer has been constructed and is presently being commissioned for use at the INE-Beamline for actinide research at the synchrotron source ANKA at FZK. We present the spectrometer's compact, modular design, optimized for attaining a wide range of energies, and first test measurement results. Examples from HRXES studies of lanthanides, actinides counter parts, are also shown.

  6. Emission spectroscopy of laser-ablated Si plasma related to nanoparticle formation

    Science.gov (United States)

    Narayanan, V.; Thareja, R. K.

    2004-01-01

    We report on the laser ablation of Si in vacuum, and in the presence of helium ambient at 1 and 10 Torr, respectively. The silicon nanoparticles were deposited on silicon substrate at room temperature by ablating silicon wafer in ambient atmosphere of helium at 1 Torr. The mean cluster size ranging from 1.8 to 4.4 nm is observed depending on the laser intensity. Optical emission spectroscopy and images of the plume are used to study the spatial and temporal variation of the silicon plasma. The electron density, measured by the Stark-broadening of Si I transition 3 p2 1S-4 s 1P0 at 390.55 nm and temperature, assuming thermal equilibrium, were found to be 1.2×10 18 cm -3 and 2 eV, respectively. The temporal variation of Si I transition 3 p2 1S-4 s 1P0 at 390.55 nm showed a shift in peak position attributed to collisions at an early stage of plasma formation. The relative concentration of Si II/Si I estimated by using the Saha-Boltzmann relation showed abundance of Si I. Time resolved images of the plume were used to investigate the dynamics of the expanding plasma plume, estimating the vapor pressure, vapor temperature, velocity, and stopping distance of the plume. The photoluminescent spectra of the Si thin films showed three distinct emission bands at 2.7, 2.2 and 1.69 eV, the origin of these bands is attributed to defects and quantum confinement.

  7. Emission Spectroscopy of Atmospheric-Pressure Ball Plasmoids: Higher Energy Reveals a Rich Chemistry

    Science.gov (United States)

    Dubowsky, Scott E.; Rose, Amber Nicole; Glumac, Nick; McCall, Benjamin J.

    2017-06-01

    Ball plasmoids (self-sustaining spherical plasmas) are a particularly unique example of a non-equilibrium air plasma. These plasmoids have lifetimes on the order of hundreds of milliseconds without an external power source, however, current models dictate that a ball plasmoid should recombine in a millisecond or less. Ball plasmoids are considered to be a laboratory analogue of natural ball lightning, a phenomenon that has eluded scientific explanation for centuries. We are searching for the underlying physicochemical mechanism(s) by which ball plasmoids and (by extension) ball lightning are stabilized using a variety of diagnostic techniques. This presentation will focus on optical emission spectroscopy (OES) of ball plasmoid discharges between 190-850 nm. The previous generation of OES measurements of this system showed emission from only a few atomic and molecular species, however, the energy available for the discharges in these experiments was limited by the size of the capacitor banks and voltages to which the capacitor banks were charged. We are capable of generating plasmoids at much higher energies, and as a result we are the first to report a very rich chemistry previously not observed in ball plasmoids. We have identified signals from species including NO A^{2}Σ^{+}→X^{2}Π, OH A^{2}Σ^{+}→X^{2}Π, NH A^{3}Π→X^{3}Σ^{-}, AlO A^{2}Π→X^{2}Σ^{+}, NH^{+} B^{2}Δ→X^{2}Π, W I, Al I, Cu I, and H_{α}, all of which have not yet been reported for this system. Analysis of the emission spectra and fitting procedures will be discussed, rotational temperatures of constituent species will be reported, and theories of ball plasmoid stabilization based upon these new results will be presented. Versteegh, A.; Behringer, K.; Fantz, U.; Fussman, G.; Jüttner, B.; Noack, S. Plas. Sour. Sci. Technol. 2008, 17(2), 024014 Stephan, K. D.; Dumas, S.; Komala-Noor, L.; McMinn, J. Plas. Sour. Sci. Technol. 2013, 22(2), 025018

  8. Ultra-nonlocality in density functional theory for photo-emission spectroscopy.

    Science.gov (United States)

    Uimonen, A-M; Stefanucci, G; van Leeuwen, R

    2014-05-14

    We derive an exact expression for the photocurrent of photo-emission spectroscopy using time-dependent current density functional theory (TDCDFT). This expression is given as an integral over the Kohn-Sham spectral function renormalized by effective potentials that depend on the exchange-correlation kernel of current density functional theory. We analyze in detail the physical content of this expression by making a connection between the density-functional expression and the diagrammatic expansion of the photocurrent within many-body perturbation theory. We further demonstrate that the density functional expression does not provide us with information on the kinetic energy distribution of the photo-electrons. Such information can, in principle, be obtained from TDCDFT by exactly modeling the experiment in which the photocurrent is split into energy contributions by means of an external electromagnetic field outside the sample, as is done in standard detectors. We find, however, that this procedure produces very nonlocal correlations between the exchange-correlation fields in the sample and the detector.

  9. A study of adulteration in gasoline samples using flame emission spectroscopy and chemometrics tools.

    Science.gov (United States)

    de Paulo, Jaqueline M; Mendes, Gisele; Barros, José E M; Barbeira, Paulo J S

    2012-12-21

    This work presents a low cost system based on Flame Emission Spectroscopy (FES) that enables the prediction of fuel adulteration. The spectral data acquired using FES were associated with chemometric tools--Partial Least Squares Discriminant Analysis (PLS-DA) and Partial Least Squares (PLS), aiming to predict gasoline adulterations with different solvents. The classification of the Brazilian adulterated gasoline samples with turpentine, thinner, kerosene, rubber solvent and ethanol was carried out through a PLS-DA model built using five latent variables (LV) with an accumulated variance of 100% on X and 76.78% on Y. The combination of these techniques provided the discrimination of distinct groups for each one of the studied adulterants. Subsequent to the classification, samples of adulterated gasoline with the same solvents with contents varying from 1 to 50% (v/v) were analyzed through FES and multivariate calibration curves were employed in order to predict the contents of the respective solvents. The results obtained by the combination of FES and PLS provided the determination of gasoline adulterants with small calibration and validation errors and also lower values than the ones reported in the literature using other spectroscopic techniques.

  10. Dynamics of Bloch State Positronium Emission from MOF Targets Studied via Rydberg TOF Spectroscopy

    Science.gov (United States)

    Piñeiro Escalera, Alina; Jones, Adric; Mills, Allen

    2016-05-01

    Recent advances in the efficient production and detection of Rydberg positronium (Ps) have made it possible to perform energy- and angle- resolved time-of-flight (TOF) spectroscopy with Ps. We report here TOF measurements of Ps emission from the metal-oxide framework (MOF) targets, MOF-5 and ZIF-8. MOFs are a recently synthesized class of chemical structures, characterized by high long-range order and large surface area to volume ratios (i.e., they are highly porous and uniform, crystalline materials). Ps is found to be emitted predominantly in a series of monoenergetic peaks, providing clear evidence of Ps Bloch states. Measuring the relative populations of the monoenergetic peaks, as a function of implantation energy and target temperature, provides insight into the target-dependent dynamics of Bloch state Ps. Work supported by the U.S. National Science Foundation Grants No. PHY 1206100 and No. PHY 1040590 and the National Science Foundation Graduate Research Fellowship Progam (NSF-GRFP). DOE BES DE-FG02-13ER46972 (MOF-5 synthesis and characterization).

  11. Plasma Wind Tunnel Investigation of European Ablators in Nitrogen/Methane Using Emission Spectroscopy

    Directory of Open Access Journals (Sweden)

    Ricarda Wernitz

    2013-01-01

    Full Text Available For atmospheric reentries at high enthalpies ablative heat shield materials are used, such as those for probes entering the atmosphere of Saturn’s moon Titan, such as Cassini-Huygens in December, 2004. The characterization of such materials in a nitrogen/methane atmosphere is of interest. A European ablative material, AQ60, has been investigated in plasma wind tunnel tests at the IRS plasma wind tunnel PWK1 using the magnetoplasma dynamic generator RD5 as plasma source in a nitrogen/methane atmosphere. The dimensions of the samples are 45 mm in length with a diameter of 39 mm. The actual ablator has a thickness of 40 mm. The ablator is mounted on an aluminium substructure. The experiments were conducted at two different heat flux regimes, 1.4 MW/m2 and 0.3 MW/m2. In this paper, results of emission spectroscopy at these plasma conditions in terms of plasma species’ temperatures will be presented, including the investigation of the free-stream species, N2 and N2+, and the major erosion product C2, at a wavelength range around 500 nm–600 nm.

  12. Synthetic diagnostic for the beam emission spectroscopy diagnostic using a full optical integration

    Science.gov (United States)

    Hausammann, L.; Churchill, R. M.; Shi, L.

    2017-02-01

    The beam emission spectroscopy (BES) diagnostic is used to measure fluctuations of electron density in the edge and core of fusion plasmas, and is a key in understanding turbulence in a plasma reactor. A synthetic BES diagnostic for the turbulence simulation code XGC1 has been developed using a realistic neutral beam model and an optical system easily adaptable to different kinds of tokamaks. The beam is modeled using multiple beam energy components, each one with a fraction of the total energy and their own mass and energy (mono-energetic components). The optical system consists of a lens focusing a bundle of optical fibers and resulting in a 2D measurement. The synthetic diagnostic gives similar correlation functions and behaviour of the turbulences than the usual methods that do not take into account the full 3D optical effects. The results, based on a simulation of XGC1, contain an analysis of the correlation (in space and time), a comparison of different approximations possible and their importance in accurately modeling the BES diagnostic.

  13. Observation of iron spin-states using tabletop x-ray emission spectroscopy and microcalorimeter sensors

    Science.gov (United States)

    Joe, Y. I.; O'Neil, G. C.; Miaja-Avila, L.; Fowler, J. W.; Jimenez, R.; Silverman, K. L.; Swetz, D. S.; Ullom, J. N.

    2016-01-01

    X-ray emission spectroscopy (XES) is a powerful probe of the electronic and chemical state of elemental species embedded within complex compounds. X-ray sensors that combine high resolving power and high collecting efficiency are desirable for photon-starved XES experiments such as measurements of dilute, gaseous, and radiation-sensitive samples, time-resolved measurements, and in-laboratory XES. To assess whether arrays of cryogenic microcalorimeters will be useful in photon-starved XES scenarios, we demonstrate that these emerging energy-dispersive sensors can detect the spin-state of 3d electrons of iron in two different compounds, Fe2O3 and FeS2. The measurements were conducted with a picosecond pulsed laser-driven plasma as the exciting x-ray source. The use of this tabletop source suggests that time-resolved in-laboratory XES will be possible in the future. We also present simulations of {{K}}α and {{K}}β spectra that reveal the spin-state sensitivity of different combinations of sensor resolution and accumulated counts. These simulations predict that our current experimental apparatus can perform time-resolved XES measurements on some samples with a measurement time of a few 10 s of hours per time delay.

  14. Trace cobalt speciation in bacteria and at enzymic active sites using emission Moessbauer spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kamnev, A.A.; Antonyuk, L.P.; Smirnova, V.E.; Serebrennikova, O.B. [Laboratory of Biochemistry, Institute of Biochemistry and Physiology of Plants and Microorganisms, Russian Academy of Sciences, Saratov (Russian Federation); Kulikov, L.A.; Perfiliev, Yu.D. [Laboratory of Nuclear Chemistry Techniques, Department of Radiochemistry, Faculty of Chemistry, Moscow State University (Russian Federation)

    2002-02-01

    {sup 57}Co emission Moessbauer spectroscopy (EMS) allows the chemical state of cobalt, as influenced by its coordination environment, to be monitored in biological samples at its physiological (trace) concentrations. To draw attention to EMS as a valuable tool for speciation of cobalt in biocomplexes, the process of cobalt(II) metabolism in cells of the plant growth-promoting rhizobacterium Azospirillum brasilense Sp245 was investigated using EMS of {sup 57}Co{sup II}-doped bacterial cells. EMS measurements also showed {sup 57}Co{sup II}-activated glutamine synthetase (GS, a key enzyme of nitrogen metabolism, isolated from this bacterium) to have two different cobalt(II) forms at its active sites, in agreement with data available on other bacterial GSs. Chemical after-effects following electron capture by the nucleus of the parent {sup 57}Co{sup II} during the {sup 57}Co{yields}{sup 57}Fe transition, which contribute to the formation of a stabilised daughter {sup 57}Fe{sup III} component along with the nucleogenic {sup 57}Fe{sup II} forms, are also briefly considered. (orig.)

  15. VUV emission spectroscopy combined with H- density measurements in the ion source Prometheus I

    Science.gov (United States)

    Aleiferis, S.; Laulainen, J.; Svarnas, P.; Tarvainen, O.; Bacal, M.; Béchu, S.

    2017-08-01

    "Prometheus I" is a volume H- negative ion source, driven by a network of dipolar electron cyclotron resonance (ECR; 2.45 GHz) modules. The vacuum-ultraviolet (VUV) emission spectrum of low-temperature hydrogen plasmas may be related to molecular and atomic processes involved directly or indirectly in the production of negative ions. In this work, VUV spectroscopy has been performed in the above source, Prometheus I, both in the ECR zones and the bulk (far from ECR zones and surfaces) plasma. The acquired VUV spectra are correlated with the negative ion densities, as measured by means of laser photodetachment, and the possible mechanisms of negative ion production are considered. The well-established H- formation process of dissociative attachment to vibrationally excited molecules is evaluated, while an additional production path (i.e. neutral resonant ionization) is tested due to the recently attracted interest. The obtained results indicate that for the source Prometheus I, the dominant formation process is dissociative attachment.

  16. Optical Emission Spectroscopy in PECVD Helps Modulate Key Features in Biofunctional Coatings for Medical Implants

    Science.gov (United States)

    Santos, Miguel; Michael, Praveesuda; Filipe, Elysse; Wise, Steven; Bilek, Marcela; University of Sydney Collaboration

    2015-09-01

    We explore the use of optical emission spectroscopy (OES) diagnostic tools as a process feedback control strategy in plasma-assisted deposition of biofunctional coatings. Hydrogenated carbon nitride coatings are deposited on medical-grade metallic substrates using radio-frequency (rf) discharges sustained in C2H2/N2/Ar gaseous mixtures. The discharge is generated by capacitively coupling the rf power (supplied at f = 13.56 MHz) to the plasma and the substrates are electrically biased using a pulse generator to provide microsecond square profiled pulses at voltages in the range |Vbias| = 250 V - 1000 V. Nitrogen content and CN bonding configurations in the coatings follow similar trends to those of CN radicals and nitrogen molecular ions in the discharge. OES is used as a non-intrusive diagnostic technique to identify a suitable window of process parameters and ultimately achieve biofunctional interfaces compatible with current clinical demands. Importantly, we demonstrate that key features of the coatings can be modulated and made suitable for blood and/or tissue contacting medical implants, such as coronary stents and orthopaedic implants. The coatings are mechanically robust, inherently non-thrombogenic and can be readily modified, enabling an easy functionalization through the immobilization of biological molecules in a bioactive conformation.

  17. Assessment of diabetic neuropathy with emission tomography and magnetic resonance spectroscopy.

    Science.gov (United States)

    Rao, Harshvardhan; Gaur, Neeraj; Tipre, Dnyanesh

    2017-04-01

    Diabetic neuropathies (DNs) are nerve-damaging disorders associated with diabetes. They are commonly attributed to peripheral nerves and primarily affect the limbs of the patient. They cause altered sensitivity to external stimuli along with loss in balance and reflexes of the affected patient. DNs are associated with a variety of clinical manifestations including autonomic failure and are caused by poor management of blood sugar levels. Imaging modalities provide vital information about early physiological changes in DNs. This review summarizes contributions by various teams of scientists in developing imaging methods to assess physiological changes in DNs and ongoing clinical trials where imaging modalities are applied to evaluate therapeutic intervention in DNs. Development of PET, single photon emission computed tomography, and magnetic resonance spectroscopy methods over the past 20 years are reviewed in the diagnostic assessment of DNs. Abnormal radiotracer pharmacokinetics and neurometabolite spectra in affected organs confirm physiological abnormalities in DN. With the use of the Siemens Biograph mMR and GE Signa - 60 cm (PET/MRI scanner), simultaneous acquisition of physiological and anatomical information could enhance understanding of DNs and accelerate drug development.

  18. Time-resolved measurement of emission profiles in pulsed radiofrequency glow discharge optical emission spectroscopy: Investigation of the pre-peak

    Energy Technology Data Exchange (ETDEWEB)

    Alberts, D. [Department of Physical and Analytical Chemistry, Faculty of Chemistry, University of Oviedo, Julian Claveria 8, 33006 Oviedo (Spain); Horvath, P. [Swiss Federal Laboratories for Materials Testing and Research (EMPA), Feuerwerkerstrasse 39, 3602 Thun (Switzerland); Nelis, Th. [LAPLACE, Universite Paul Sabatier, 118 rte de Narbonne, Bat3R2, 31062 Toulouse Cedex (France); CU Jean Francois Champollion, Place de Verdun 81012 Albi Cedex 9 (France); Pereiro, R. [Department of Physical and Analytical Chemistry, Faculty of Chemistry, University of Oviedo, Julian Claveria 8, 33006 Oviedo (Spain); Bordel, N. [Department of Physics, Faculty of Science, University of Oviedo, Calvo Sotelo, 33007 Oviedo (Spain); Michler, J. [Swiss Federal Laboratories for Materials Testing and Research (EMPA), Feuerwerkerstrasse 39, 3602 Thun (Switzerland); Sanz-Medel, A., E-mail: asm@uniovi.e [Department of Physical and Analytical Chemistry, Faculty of Chemistry, University of Oviedo, Julian Claveria 8, 33006 Oviedo (Spain)

    2010-07-15

    Radiofrequency glow discharge coupled to optical emission spectroscopy has been used in pulsed mode in order to perform a detailed study of the measured temporal emission profiles for a wide range of copper transitions. Special attention has been paid to the early emission peak (or so-called pre-peak), observed at the beginning of the emission pulse profile. The effects of the important pulse parameters such as frequency, duty cycle, pulse width and power-off time, have been studied upon the Cu pulse emission profiles. The influence of discharge parameters, such as pressure and power, was studied as well. Results have shown that the intensity observed in the pre-peak can be 10 times as large as the plateau value for resonant lines and up to 5 times in case of transitions to the metastable levels. Increasing pressure or power increased the pre-peak intensity while its appearance in time changed. The pre-peak decreased when the discharge off-time was shorter than 100 {mu}s. According to such results, the presence of the pre-peak could be probably due to the lack of self-absorption during the first 50 {mu}s, and not to the ignition of the plasma. Under the selected operation conditions, the use of the pre-peak emission as analytical signals increases the linearity of calibration curves for resonant lines subjected to self-absorption at high concentrations.

  19. Spectroscopy

    DEFF Research Database (Denmark)

    Berg, Rolf W.

    This introductory booklet covers the basics of molecular spectroscopy, infrared and Raman methods, instrumental considerations, symmetry analysis of molecules, group theory and selection rules, as well as assignments of fundamental vibrational modes in molecules.......This introductory booklet covers the basics of molecular spectroscopy, infrared and Raman methods, instrumental considerations, symmetry analysis of molecules, group theory and selection rules, as well as assignments of fundamental vibrational modes in molecules....

  20. Method to obtain absolute impurity density profiles combining charge exchange and beam emission spectroscopy without absolute intensity calibrationa)

    Science.gov (United States)

    Kappatou, A.; Jaspers, R. J. E.; Delabie, E.; Marchuk, O.; Biel, W.; Jakobs, M. A.

    2012-10-01

    Investigation of impurity transport properties in tokamak plasmas is essential and a diagnostic that can provide information on the impurity content is required. Combining charge exchange recombination spectroscopy (CXRS) and beam emission spectroscopy (BES), absolute radial profiles of impurity densities can be obtained from the CXRS and BES intensities, electron density and CXRS and BES emission rates, without requiring any absolute calibration of the spectra. The technique is demonstrated here with absolute impurity density radial profiles obtained in TEXTOR plasmas, using a high efficiency charge exchange spectrometer with high etendue, that measures the CXRS and BES spectra along the same lines-of-sight, offering an additional advantage for the determination of absolute impurity densities.

  1. Method to obtain absolute impurity density profiles combining charge exchange and beam emission spectroscopy without absolute intensity calibration

    Energy Technology Data Exchange (ETDEWEB)

    Kappatou, A.; Delabie, E. [FOM Institute DIFFER - Dutch Institute for Fundamental Energy Research, Association EURATOM-FOM, 3430 BE Nieuwegein (Netherlands); Jaspers, R. J. E.; Jakobs, M. A. [Science and Technology of Nuclear Fusion, Eindhoven University of Technology, 5600 MB Eindhoven (Netherlands); Marchuk, O.; Biel, W. [Institute for Energy and Climate Research, Forschungszentrum Julich GmbH, Trilateral Euregio Cluster, 52425 Julich (Germany)

    2012-10-15

    Investigation of impurity transport properties in tokamak plasmas is essential and a diagnostic that can provide information on the impurity content is required. Combining charge exchange recombination spectroscopy (CXRS) and beam emission spectroscopy (BES), absolute radial profiles of impurity densities can be obtained from the CXRS and BES intensities, electron density and CXRS and BES emission rates, without requiring any absolute calibration of the spectra. The technique is demonstrated here with absolute impurity density radial profiles obtained in TEXTOR plasmas, using a high efficiency charge exchange spectrometer with high etendue, that measures the CXRS and BES spectra along the same lines-of-sight, offering an additional advantage for the determination of absolute impurity densities.

  2. Measurements of methane emissions from landfills using mobile plume method with trace gas and cavity ring-down spectroscopy

    Science.gov (United States)

    Mønster, J.; Kjeldsen, P.; Scheutz, C.

    2012-04-01

    Methane is emitted to the atmosphere from both anthropogenic and natural sources. One of the major anthropogenic sources is methane produced by bacteria in anaerobic environments such as rice pads and landfills. Land filling has for many years been the preferred waste disposal method, resulting in a large methane production with a large contribution to the global increase in atmospheric green house gas concentration. Several steps have been taken to reduce the emission of methane from landfills. In order to validate the effect of these steps, a measurement method is needed to quantify methane emissions with a large spatial variation. One method is to use a highly sensitive and fast analytical method, capable of measuring the atmospheric concentration methane downwind from emission areas. Combined with down-wind measurements of a trace gas, emitted at a controlled mass flow rate, the methane emission can be calculated. This method is called the mobile plume method, as the whole plume is measured by doing several transects. In the current study a methane/acetylene analyzer with cavity ring-down spectroscopy detection (Picarro, G2203) was used to estimate methane from a number of Danish landfills. We measured at both active and closed landfills and investigated the difference in methane emission. At landfills where the emissions could have more than one origin, the source strength of the different emission areas was determined by accurate trace gas positioning and choosing appropriate wind speed and measurement distance. To choose these factors, we addressed the uncertainties and limitations of the method with respect to the configuration of the trace gas bottles and the distance between the emission area and the measurement points. Composting of organic material in large piles was done at several of the investigated landfills and where possible, the methane emission from this partly anaerobic digestion was measured as a separate emission.

  3. A Chemical Detector for Gas Chromatography Using Pulsed Discharge Emission Spectroscopy on a Microchip

    Science.gov (United States)

    Luo, X.; Zhu, W.; Mitra, B.; Liu, J.; Liu, T.; Fan, X.; Gianchandani, Y.

    2011-12-01

    There is increasing interest in miniaturized systems for chemical analysis in harsh environments. Chemical detection by emission spectroscopy of on-chip microdischarges [1-3] can be performed at >200°C [4], suggesting utility inspace exploration, volcanic monitoring, and oil well monitoring. This abstract describes the first use of pulsed microdischarge spectroscopy for gas chromatography (GC).This effort supports NASA interests in monitoring closed-loop life support systems for spacecraft. The microdischarge occurs on a 1cm2 glass chip (Fig. 1a), with thin-film Ni electrodes separated by 160μm. A glass lid with a grooved gas-flow channel, and inlet/outlet capillary tubes are epoxy-sealed to the chip. Located downstream of the 1.7m-long, RTX-1-coated, GC separation column, the microdischarge chip is read by a spectrometer. In a typical experiment (Fig. 1b), a mixture of acetone 3.6μg, 1-hexanol 2.8μg and nitrobenzene 3.0μg, is injected, with He carrier gas at 1.56sccm, through the GC. Acetone elutes quickly while nitrobenzene is slower. Microdischarges are triggered at 0.5Hz for 6 min., and 0.04Hz thereafter. Each microdischarge consumes ≈8mJ; the average power is ≈1.14mW. The spectrum (Fig. 1b, inset) shows that the 388nm peak, representing CN/CH fragments [5], is enhanced by carbon compounds. Its strength relative to the 588nm peak of He provides a chromatogram. Fig. 1b also shows a benchmark result from a commercial flame ionization detector (FID). The differences in elution time are attributed to differences in the gas flow paths for the two detectors [1]. REFERENCES [1] Eijkel et al, Anal. Chem, 2000 [2] Mitra et al, IEEE Trans Plasma Sci, 2008 [3] Mitra et al, IEEE Sensors, 2008 [4] Wright et al, APL, 2009 [5] Pearse et al, The Identification of Molecular Spectra, 1963

  4. Multi-epoch Spectroscopy of Dwarf Galaxies with AGN Signatures: Identifying Sources with Persistent Broad Hα Emission

    Science.gov (United States)

    Baldassare, Vivienne F.; Reines, Amy E.; Gallo, Elena; Greene, Jenny E.; Graur, Or; Geha, Marla; Hainline, Kevin; Carroll, Christopher M.; Hickox, Ryan C.

    2016-09-01

    We use time-domain optical spectroscopy to distinguish between broad emission lines powered by accreting black holes (BHs) and stellar processes (i.e., supernovae) for 16 galaxies identified as active galactic nucleus (AGN) candidates by Reines et al (2013). Our study is primarily focused on those objects with narrow emission line ratios dominated by star formation, for which the origin of the broad Hα emission was unclear. Based on follow-up spectroscopy, we find that the broad Hα emission has faded or was ambiguous for all of the star-forming objects (14/16), over baselines ranging from 5-14 years, suggesting a transient stellar process was responsible for the broad emission in previous Sloan Digital Sky Survey observations. For the two objects in our follow-up sample with narrow-line AGN signatures (RGG 9 and RGG 119), we find persistent broad Hα emission consistent with an AGN origin. Additionally, we use high spectral resolution observations to measure stellar velocity dispersions for 15 objects in the Reines et al. (2013) sample, all with narrow-line ratios indicating the presence of an AGN. Stellar masses range from ˜ 5× {10}8 to 3× {10}9 M ⊙, and we measure {σ }* in the range of 28{--}71 {km} {{{s}}}-1. These {σ }* correspond to some of the lowest-mass galaxies with optical signatures of AGN activity. We show that RGG 119, the one object that has both a measured {σ }* and persistent broad Hα emission, falls near the extrapolation of the {\\text{}}{M}{BH}-{σ }\\star relation to the low-mass end.

  5. Investigations of the cathode region of an argon arc plasma by degenerate four-wave mixing laser spectroscopy and optical emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Dzierzega, K [Marian Smoluchowski Institute of Physics, Jagiellonian University, ul. Reymonta 4, 30-059 Cracow (Poland); Pokrzywka, B [Mt. Suhora Observatory, Cracow Pedagogical University, ul. Podchorazych 2, 30-083 Cracow (Poland); Pellerin, S [LASEP, Universite d' Orleans-Centre Universitaire de Bourges, Rue Gaston Berger BP 4043, 18028 Bourges (France)

    2004-07-07

    Degenerate four-wave mixing (DFWM) laser spectroscopy was used in local studies of atmospheric pressure argon plasma generated in a free-burning arc. The results of plasma diagnostics using the DFWM method were compared to the results obtained with optical emission measurements. In the cathode region of the arc the maxima of both the DFWM signal and the emission coefficient for the 696.5 nm Ar I line depend on the distance from the cathode tip. This effect proves the departure of the plasma state from local thermal equilibrium (LTE) as it has been reported by many authors. On the other hand the Stark shifts of the 696.5 nm Ar I line determined by the DFWM method in relation to plasma diagnostic results show no deviations from LTE on the arc axis down to 1.0 mm from the cathode tip.

  6. Soft X-ray emission spectroscopy of liquids and lithium batterymaterials

    Energy Technology Data Exchange (ETDEWEB)

    Augustsson, Andreas [Uppsala Univ. (Sweden)

    2004-01-01

    Lithium ion insertion into electrode materials is commonly used in rechargeable battery technology. The insertion implies changes in both the crystal structure and the electronic structure of the electrode material. Side-reactions may occur on the surface of the electrode which is exposed to the electrolyte and form a solid electrolyte interface (SEI). The understanding of these processes is of great importance for improving battery performance. The chemical and physical properties of water and alcohols are complicated by the presence of strong hydrogen bonding. Various experimental techniques have been used to study geometrical structures and different models have been proposed to view the details of how these liquids are geometrically organized by hydrogen bonding. However, very little is known about the electronic structure of these liquids, mainly due to the lack of suitable experimental tools. In this thesis examples of studies of lithium battery electrodes and liquid systems using soft x-ray emission spectroscopy will be presented. Monochromatized synchrotron radiation has been used to accomplish selective excitation, in terms of energy and polarization. The electronic structure of graphite electrodes has been studied, before and after lithium intercalation. Changes in the electronic structure upon lithiation due to transfer of electrons into the graphite π-bands have been observed. Transfer of electrons in to the 3d states of transition metal oxides upon lithiation have been studied, through low energy excitations as dd- and charge transfer-excitations. A SEI was detected on cycled graphite electrodes. By the use of selective excitation different carbon sites were probed in the SEI. The local electronic structure of water, methanol and mixtures of the two have been examined using a special liquid cell, to separate the liquid from the vacuum in the experimental chamber. Results from the study of liquid water showed a strong influence on the 3a1 molecular

  7. Laser-induced breakdown spectroscopy application to control of the process of precious metal recovery and recycling

    Science.gov (United States)

    Legnaioli, S.; Lorenzetti, G.; Pardini, L.; Palleschi, V.; Pace, D. M. Diaz; Garcia, F. Anabitarte; Grassi, R.; Sorrentino, F.; Carelli, G.; Francesconi, M.; Francesconi, F.; Borgogni, R.

    2012-05-01

    In this paper, we discuss the application of laser-induced breakdown spectroscopy to precious metal alloys used for the control of the process of recovery and recycling of scraps and waste of industrial processes. In particular, the possibility to obtain sensitivity and trueness comparable to the current systems used in industrial environment in the quantitative determination of the elements of interest was explored. The present study demonstrates that laser-induced breakdown spectroscopy can be considered as a viable alternative to inductively coupled plasma optical emission spectrometry and X-ray fluorescence spectroscopy for the determination of recovered precious metals. The limits of detection obtained are of the order of 0.2 mg/g for all the elements considered. The maximum deviation with respect to the nominal concentrations is around 1 mg/g at concentrations around 20 mg/g (gold) corresponding to a relative error slightly higher than ± 5%.

  8. Proton magnetic resonance spectroscopy and single photon emission CT in patients with olivopontocerebellar atrophy

    Energy Technology Data Exchange (ETDEWEB)

    Ikuta, Naomi [Yamaguchi Univ., Ube (Japan). School of Medicine

    1998-04-01

    Using proton magnetic resonance spectroscopy ({sup 1}H-MRS) and single photon emission CT (SPECT), the cerebellum of patients with olivopontocerebellar atrophy (OPCA) and of age-matched control subjects was studied. A spectrum was collected from a 27 cm{sup 3} (3 x 3 x 3 cm) voxel in the cerebellum containing white and gray matters in order to measure the distribution and relative signal intensities of N-acetylaspartate (NAA), creatine (Cre) and choline (Cho). In the cerebellum of the patients with OPCA, mean NAA/Cre ratios for OPCA patients were significantly decreased compared with normal control subjects (OPCA, 1.01{+-}0.247; controls, 1.526{+-}0.144: p<0.001). Mean NAA/Cho ratios for OPCA patients were slightly decreased (OPCA, 1.285{+-}0.228; controls 1.702{+-}0.469: p<0.06). Cho/Cre ratios valued in the cerebellum of OPCA patients were not significantly different from those in normal controls (OPCA, 0.793{+-}0.186; controls, 0.946{+-}0.219). The ratio of RI count in the cerebellum to that in the occipital lobe was significantly decreased in OPCA patients (OPCA, 0.947{+-}0.096; controls, 1.06{+-}0.063: p<0.01). Cerebellar signs were assessed including gait ataxia, limb ataxia, dysarthria, saccadic pursuit, and nystagmus separately or in combination. In patients with more severe ataxic gait and dysarthria, MRS revealed slightly lowered NAA/Cre ratio. There was no significant correlation between NAA/Cre ratio and severity of other clinical signs. The MRS and SPECT findings give a confirmative evidence of hypofunction in cerebellum of patients with OPCA. (author)

  9. Beam characterization by means of emission spectroscopy in the ELISE test facility

    Science.gov (United States)

    Barbisan, M.; Bonomo, F.; Fantz, U.; Wünderlich, D.

    2017-05-01

    The ELISE (extraction from a large ion source experiment) test facility at IPP Garching hosts a RF H -/D - ion source and an acceleration system. Its target is to demonstrate the performance foreseen for the ITER neutral beam injector (NBI) system in terms of extracted current density (H/D), fraction of co-extracted electrons and pulse duration. The size of the ELISE extraction area is half that foreseen for the ITER NBI. This paper presents a detailed study of the ELISE beam divergence and uniformity. In particular, it was possible to describe the beam as the sum of two components at very different divergence: about 2° versus 5° ÷ 7°. As test cases, the beam properties have been measured as function of two source parameters. The first one is the current flowing through the grid facing the plasma, the plasma grid (PG), in order to generate the magnetic filter field. The second one is the bias current flowing between the PG and the source walls. Both the filter field and the bias current influence the fraction of co-extracted electrons, but also the properties of the plasma just in front of the extraction system and the beam properties. The divergence and the uniformity of the beam have been measured by a beam emission spectroscopy (BES) diagnostic; the detailed analysis of the raw spectra collected by BES led to describing the beam with two components of different divergence. This concept has been supported by the information given by thermal imaging of the diagnostic calorimeter. Further support to the proposed beam model has been found in the behavior of the currents flowing in the acceleration system and beamline components; these currents are given by the most divergent (charged) particles of the beam.

  10. Characterization of a high current pulsed arc using optical emission spectroscopy

    Science.gov (United States)

    Sousa Martins, R.; Zaepffel, C.; Chemartin, L.; Lalande, Ph; Soufiani, A.

    2016-10-01

    In this paper, we present the investigation realized on an experimental setup that simulates an arc column subjected to the transient phase of a lightning current waveform in laboratory conditions. Optical emission spectroscopy is employed to assess space- and time-resolved properties of this high current pulsed arc. Different current peak levels are utilised in this work, ranging from 10 kA to 100 kA, with a peak time around 15 µs. Ionic lines of nitrogen and oxygen are used to determine the radial profiles of temperature and electron density of the arc channel over time from 2 µs to 36 µs. A combination of 192 N II and O II lines is considered in the calculation of the bound-bound contribution of the absorption coefficient of the plasma channel. Calculations of the optical thickness showed that self-absorption of these ionic lines in the arc column is important. To obtain temperature and electron density profiles in the arc, we solved the radiative transfer equation across the channel under an axisymmetric assumption and considering the channel formed by uniform concentric layers. For the 100 kA current peak level, the temperature reaches more than 38 000 K and the electron density reaches 5  ×  1018 cm-3. The pressure inside the channel is calculated using the air plasma composition at local thermodynamic equilibrium, and reaches 45 bar. The results are discussed and utilised to estimate the electrical conductivity of the arc channel.

  11. Optical emission spectroscopy diagnostics of an atmospheric pressure direct current microplasma jet

    Energy Technology Data Exchange (ETDEWEB)

    Sismanoglu, B.N., E-mail: bogos@ita.b [Departamento de Fisica, Instituto Tecnologico de Aeronautica, Comando-Geral de Tecnologia Aeroespacial, Pca Marechal Eduardo Gomes 50, 12 228-900, Sao Jose dos Campos, SP (Brazil); Amorim, J., E-mail: jayr.amorim@bioetanol.org.b [Centro de Ciencia e Tecnologia do Bioetanol - CTBE, Caixa Postal 6170, 13083-970 Campinas, Sao Paulo (Brazil); Souza-Correa, J.A., E-mail: jorge.correa@bioetanol.org.b [Centro de Ciencia e Tecnologia do Bioetanol - CTBE, Caixa Postal 6170, 13083-970 Campinas, Sao Paulo (Brazil); Oliveira, C., E-mail: carlosf@ita.b [Departamento de Fisica, Instituto Tecnologico de Aeronautica, Comando-Geral de Tecnologia Aeroespacial, Pca Marechal Eduardo Gomes 50, 12 228-900, Sao Jose dos Campos, SP (Brazil); Gomes, M.P., E-mail: gomesmp@ita.b [Departamento de Fisica, Instituto Tecnologico de Aeronautica, Comando-Geral de Tecnologia Aeroespacial, Pca Marechal Eduardo Gomes 50, 12 228-900, Sao Jose dos Campos, SP (Brazil)

    2009-11-15

    This paper is about the use of optical emission spectroscopy as a diagnostic tool to determine the gas discharge parameters of a direct current (98% Ar-2% H{sub 2}) non-thermal microplasma jet, operated at atmospheric pressure. The electrical and optical behaviors were studied to characterize this glow discharge. The microplasma jet was investigated in the normal and abnormal glow regimes, for current ranging from 10 to 130 mA, at approx 220 V of applied voltage for copper cathode. OH (A {sup 2}SIGMA{sup +}, nu = 0 -> X {sup 2}PI, nu' = 0) rotational bands at 306.357 nm and also the 603.213 nm Ar I line, which is sensitive to van der Waals broadening, were used to determine the gas temperature, which ranges from 550 to 800 K. The electron number densities, ranging from 6.0 x 10{sup 14} to 1.4 x 10{sup 15} cm{sup -3}, were determined through a careful analysis of the main broadening mechanisms of the H{sub beta} line. From both 603.213 nm and 565.070 nm Ar I line broadenings, it was possible to obtain simultaneously electron number density and temperature (approx 8000 K). Excitation temperatures were also measured from two methods: from two Cu I lines and from Boltzmann-plot of 4p-4s and 5p-4s Ar I transitions. By employing H{sub alpha} line, the hydrogen atoms' H temperature was estimated (approx 18,000 K) and found to be surprisingly hotter than the excitation temperature.

  12. Characterization of a direct dc-excited discharge in water by optical emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Bruggeman, Peter; Leys, Christophe [Department of Applied Physics, Ghent University, Jozef Plateaustraat 22, B-9000 Ghent (Belgium); Schram, Daan [Department of Applied Physics, Technische Universiteit Eindhoven, PO Box 513, 5600 MB Eindhoven (Netherlands); Gonzalez, Manuel A [Departamento de Fisica Aplicada, Universidad de Valladolid, 47011 Valladolid (Spain); Rego, Robby [Flemish Institute of Technological Research, VITO Materials, Boeretang 200, B-2400 Mol (Belgium); Kong, Michael G [Department of Electronic and Electrical Engineering, Loughborough University, Loughborough, Leicestershire LE11 3TU (United Kingdom)], E-mail: peter.bruggeman@ugent.be

    2009-05-01

    Dc-excited discharges generated in water at the tip of a tungsten wire which is located at the orifice of a quartz capillary are investigated by time-averaged optical emission spectroscopy. Two distinctive discharge modes are observed. For small conductivities of the liquid the discharge is a streamer-like discharge in the liquid itself (liquid mode). For conductivities above typically 45 {mu}S cm{sup -1} a large vapour bubble is formed and a streamer discharge in this vapour bubble is observed (bubble mode). Plasma temperatures and electron densities are investigated for both modes. The gas temperature is estimated from the rotational temperature of N{sub 2}(C-B) and is 1600 {+-} 200 K for the bubble mode and 1900 {+-} 200 K for the liquid mode. The rotational temperature of OH(A-X) is up to 2 times larger and cannot be used as an estimate for the gas temperature. The rotational population distribution of OH(A), {nu} = 0 is also non-Boltzmann with a large overpopulation of high rotational states. This discrepancy in rotational temperatures is discussed in detail. Electron densities are obtained from the Stark broadening of the hydrogen Balmer beta line. The electron densities in the liquid mode are of the order of 10{sup 21} m{sup -3}. In the bubble mode electron densities are significantly smaller: (3-4) x 10{sup 20} m{sup -3}. These values are compared with the Stark broadening of the hydrogen alpha and gamma lines and with electron densities obtained from current density measurements. The chemical reactivities of the bubble and liquid modes are compared by means of the hydrogen peroxide production rate.

  13. Curve of growth methodology applied to laser-induced plasma emission spectroscopy

    Science.gov (United States)

    Gornushkin, I. B.; Anzano, J. M.; King, L. A.; Smith, B. W.; Omenetto, N.; Winefordner, J. D.

    1999-04-01

    The curve-of-growth (COG) method was applied to a laser-induced plasma. The plasma was produced by a Nd:YAG laser on the surface of steel samples containing 0.007-1.3% of Cr. The emission was collected from the top of the plasma by means of a 45° pierced mirror and aligned onto an intensified charge-coupled device (ICCD) with a gate width of 1 μs and a variable delay time. The resonance 425.4 nm Cr line was used for construction of the COG. The temperature of the plasma (˜8000 K at 5-μs delay) was determined from a Boltzmann plot. The damping constant a, proportional to the ratio of the Lorentzian to the Doppler line widths, was found from the best fit of a series of calculated COG to the experimental data points and was 0.20±0.05. The number density of neutral Cr atoms which corresponded to the transition between low and high optical densities, was ≈6.5·10 12 cm -3. The cross-section for broadening collisions of Cr atoms with atmospheric species (presumably N 2) was calculated to be (66±16) Å. The shape of the 425.4-nm Cr line was additionally checked by scanning an ultra-narrow cw Ti:Sapphire laser across the atomic transition and found to be in agreement with preliminary estimates. The potential of the COG method for laser breakdown spectroscopy is discussed.

  14. Avalanche dynamics of structural phase transitions in shape memory alloys by acoustic emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Ludwig, Benno

    2009-09-24

    In this work the avalanche dynamics of five shape memory samples has been analyzed by acoustic emission spectroscopy. The acoustic emission spectroscopy is particularly suitable for this analysis as it couples with high sensitivity to small structural changes caused by nucleation processes, interface movements, or variant rearrangements [91]. Owing to its high time resolution it provides a statistical approach to describe the jerky and intermittent character of the avalanche dynamics [20]. Rate-dependent cooling and heating runs have been conducted in order to study time-dependent aspects of the transition dynamics of the single crystals Ni{sub 63}Al{sub 37}, Au{sub 50.5}Cd{sub 49.5}, and Fe{sub 68.8}Pd{sup single}{sub 31.2}, and the polycrystalline sample Fe{sub 68.8}Pd{sup poly}{sub 31.2}. Moreover, a ferromagnetic Ni{sub 52}Mn{sub 23}Ga{sub 25} single crystal has been studied by temperature cycles under an applied magnetic field and additionally by magnetic-field cycles at a constant temperature in the martensitic phase. All samples analyzed in this work show power law behavior in the acoustic emission features amplitude, energy, and duration, which indicates scale-free behavior. The access to these power law spectra allows an investigation of energy barriers separating the metastable states, which give rise to avalanche transition dynamics. By performing rate-dependent experiments the importance of thermal fluctuations and the impact of martensite respectively twin stabilization processes have been examined. In the case of the Ni{sub 52}Mn{sub 23}Ga{sub 25} sample, the magnetic-field-induced variant rearrangement at slow field cycles leads to stronger signals than the rearrangement at quick cycles. This behavior can be explained by twin stabilization processes, which are accompanied by a reduction of the twin boundary mobility. For Ni{sub 63}Al{sub 37}, the combination of relevant thermal fluctuations, different involved time scales, and a high degree of

  15. Avalanche dynamics of structural phase transitions in shape memory alloys by acoustic emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Ludwig, Benno

    2009-09-24

    In this work the avalanche dynamics of five shape memory samples has been analyzed by acoustic emission spectroscopy. The acoustic emission spectroscopy is particularly suitable for this analysis as it couples with high sensitivity to small structural changes caused by nucleation processes, interface movements, or variant rearrangements [91]. Owing to its high time resolution it provides a statistical approach to describe the jerky and intermittent character of the avalanche dynamics [20]. Rate-dependent cooling and heating runs have been conducted in order to study time-dependent aspects of the transition dynamics of the single crystals Ni{sub 63}Al{sub 37}, Au{sub 50.5}Cd{sub 49.5}, and Fe{sub 68.8}Pd{sup single}{sub 31.2}, and the polycrystalline sample Fe{sub 68.8}Pd{sup poly}{sub 31.2}. Moreover, a ferromagnetic Ni{sub 52}Mn{sub 23}Ga{sub 25} single crystal has been studied by temperature cycles under an applied magnetic field and additionally by magnetic-field cycles at a constant temperature in the martensitic phase. All samples analyzed in this work show power law behavior in the acoustic emission features amplitude, energy, and duration, which indicates scale-free behavior. The access to these power law spectra allows an investigation of energy barriers separating the metastable states, which give rise to avalanche transition dynamics. By performing rate-dependent experiments the importance of thermal fluctuations and the impact of martensite respectively twin stabilization processes have been examined. In the case of the Ni{sub 52}Mn{sub 23}Ga{sub 25} sample, the magnetic-field-induced variant rearrangement at slow field cycles leads to stronger signals than the rearrangement at quick cycles. This behavior can be explained by twin stabilization processes, which are accompanied by a reduction of the twin boundary mobility. For Ni{sub 63}Al{sub 37}, the combination of relevant thermal fluctuations, different involved time scales, and a high degree of

  16. Development of Advanced Electrochemical Emission Spectroscopy for Monitoring Corrosion in Simulated DOE Liquid Waste

    Energy Technology Data Exchange (ETDEWEB)

    Digby Macdonald; Brian Marx; Balaji Soundararajan; Morgan Smith

    2005-07-28

    The different tasks that have been carried out under the current program are as follows: (1) Theoretical and experimental assessment of general corrosion of iron/steel in borate buffer solutions by using electrochemical impedance spectroscopy (EIS), ellipsometry and XPS techniques; (2) Development of a damage function analysis (DFA), which would help in predicting the accumulation of damage due to pitting corrosion in an environment prototypical of DOE liquid waste systems; (3) Experimental measurement of crack growth rate, acoustic emission signals, and coupling currents for fracture in carbon and low alloy steels as functions of mechanical (stress intensity), chemical (conductivity), electrochemical (corrosion potential, ECP), and microstructural (grain size, precipitate size, etc) variables in a systematic manner, with particular attention being focused on the structure of the noise in the current and its correlation with the acoustic emissions; (4) Development of fracture mechanisms for carbon and low alloy steels that are consistent with the crack growth rate, coupling current data and acoustic emissions; (5) Inserting advanced crack growth rate models for SCC into existing deterministic codes for predicting the evolution of corrosion damage in DOE liquid waste storage tanks; (6) Computer simulation of the anodic and cathodic activity on the surface of the steel samples in order to exactly predict the corrosion mechanisms; (7) Wavelet analysis of EC noise data from steel samples undergoing corrosion in an environment similar to that of the high level waste storage containers, to extract data pertaining to general, pitting and stress corrosion processes, from the overall data. The work has yielded a number of important findings, including an unequivocal demonstration of the role of chloride ion in passivity breakdown on nickel in terms of cation vacancy generation within the passive film, the first detection and characterization of individual micro fracture

  17. Development of Advanced Electrochemical Emission Spectroscopy for Monitoring Corrosion in Simulated DOE Liquid Waste

    Energy Technology Data Exchange (ETDEWEB)

    Digby D. Macdonald; Brian M. Marx; Sejin Ahn; Julio de Ruiz; Balaji Soundararaja; Morgan Smith; and Wendy Coulson

    2008-01-15

    Various forms of general and localized corrosion represent principal threats to the integrity of DOE liquid waste storage tanks. These tanks, which are of a single wall or double wall design, depending upon their age, are fabricated from welded carbon steel and contain a complex waste-form comprised of NaOH and NaNO{sub 3}, along with trace amounts of phosphate, sulfate, carbonate, and chloride. Because waste leakage can have a profound environmental impact, considerable interest exists in predicting the accumulation of corrosion damage, so as to more effectively schedule maintenance and repair. The different tasks that are being carried out under the current program are as follows: (1) Theoretical and experimental assessment of general corrosion of iron/steel in borate buffer solutions by using electrochemical impedance spectroscopy (EIS), ellipsometry and XPS techniques; (2) Development of a damage function analysis (DFA) which would help in predicting the accumulation of damage due to pitting corrosion in an environment prototypical of DOE liquid waste systems; (3) Experimental measurement of crack growth rate, acoustic emission signals and coupling currents for fracture in carbon and low alloy steels as functions of mechanical (stress intensity), chemical (conductivity), electrochemical (corrosion potential, ECP), and microstructural (grain size, precipitate size, etc) variables in a systematic manner, with particular attention being focused on the structure of the noise in the current and its correlation with the acoustic emissions; (4) Development of fracture mechanisms for carbon and low alloy steels that are consistent with the crack growth rate, coupling current data and acoustic emissions; (5) Inserting advanced crack growth rate models for SCC into existing deterministic codes for predicting the evolution of corrosion damage in DOE liquid waste storage tanks; (6) Computer simulation of the anodic and cathodic activity on the surface of the steel samples

  18. Optical emission spectroscopy of excited atoms sputtered on a Ti surface under irradiation with multicharged Ar ions

    Energy Technology Data Exchange (ETDEWEB)

    Motohashi, K [Department of Applied Physics, Tokyo University of Agriculture and Technology, 2-24-16 Koganei-shi, Tokyo 184-8588 (Japan); Saitoh, Y [Department of Advanced Radiation Technology, Takasaki Advanced Radiation Research Institute, Japan Atomic Energy Agency (JAEA), Takasaki, Gunma 370-1292 (Japan); Kitazawa, S, E-mail: motohasi@cc.tuat.ac.j [Division of ITER Project, Fusion Research Development, Japan Atomic Energy Agency (JAEA), Naka, Ibaraki 311-0193 (Japan)

    2009-04-01

    Optical emission spectroscopy of excited atoms was carried out in order to investigate the sputtering processes on solid surfaces under irradiation of slow, multicharged ions. Many atomic lines of Ti I (neutral) and Ti II (single-charged ions) were observed in wavelengths from 250 to 750 nm with irradiation by Ar{sup 3+} (30 keV) on a Ti surface which was placed in a low pressure O{sub 2} atmosphere. The emission intensity of Ti I (520 nm) decreased monotonically with an increase of O{sub 2} partial pressure, whereas that of Ti I / II (670 nm, a 2nd order wavelength of 335 nm) slightly increased. From a semi-logarithmic plot of emission intensity for the 670 nm spectrum as a function of distance from the surface, the mean velocity of the excited Ti atoms and ions in a normal direction parallel to the surface, or

  19. A Proposed Method for Measurement of Absolute Air Fluorescence Yield based on High Resolution Optical Emission Spectroscopy

    CERN Document Server

    Gika, V; Maltezos, S

    2016-01-01

    In this work, we present a method for absolute measurement of air fluorescence yield based on high resolution optical emission spectroscopy. The absolute measurement of the air fluorescence yield is feasible using the Cherenkov light, emitted by an electron beam simultaneously with the fluorescence light, as a "standard candle". The separation of these two radiations can be accomplished exploiting the "dark" spectral regions of the emission band systems of the molecular spectrum of nitrogen. In these "dark" regions the net Cherenkov light can be recorded experimentally and be compared with the calculated one. The instrumentation for obtaining the nitrogen molecular spectra in high resolution and the noninvasive method for monitoring the rotational temperature of the emission process are also described. For the experimental evaluation of the molecular spectra analysis we used DC normal glow discharges in air performed in an appropriate spectral lamp considered as an air-fluorescence light emulator. The propose...

  20. Laser Induced Emission Spectroscopy of Cold and Isolated Neutral PAHs and PANH: Implications for the red rectangle emission

    Science.gov (United States)

    Bejaoui, Salma; Salama, Farid; Sciamma O'Brien, Ella

    2016-06-01

    Blue luminescence (BL) in the emission spectra of the red rectangle centered on the bright star HD44179 is recently reported by Vijh et al [1]. This results is consistent with the broad band polarization measurements obtained in 1980 by Schmidt et al. Both experimental and theoretical studies support that BL emission could be attributed the luminescence of Polycyclic Aromatic Hydrocarbon (PAH) excited with ultraviolet light from the center of the star [4 and reference therein]. The abundance on N to C in the interstellar medium suggest also that nitrogen substituted PAH (PANH) are likely abundant in the interstellar medium [3]. They exhibit similar features as PAHs and could contribute to the unidentified spectral bands. Comparing the BL to laboratory spectra obtained on similar environment is crucial for the identification of interstellar molecules. We present in this works the absorption and the laser induced emission spectra of several isolated and cold PAHs and PANHs. Laser induced emission was performed first to PAHs and PANHs isolated in Argon matrix at 10 K. Then, measurements are performed with the supersonic jet technique of the COSmIC laboratory facility at NASA Ames. We focus, here, on the emission spectra (fluorescence and (or) phosphorescence) of these molecules and we discuss their contributions to the blue luminescence emission in the Red Rectangle nebula.[1] Vijh,U.P., Witt. A.N. & Gordon,K.D, APJ, 606, L69 (2004)[2] Schmidt, G. D., Cohen, M. & Margon, B., ApJ, 239L.133S (1980)[3] Spitzer, L., Physical Processes in the Interstellar Medium (New York Wiley-Interscience) (1978)[4] Salama, F., Galazutdinov, G. A., Kre lowski, J., Allamandola, L. J., & Musaev, F. A. ApJ, 526,(1999)

  1. Emission Line Astronomy - Coronagraphic Tunable Narrow Band Imaging and Integral Field Spectroscopy. Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose to continue our program of emission line astronomy featuring three areas of emphasis: 1) The distribution and nature of high redshift emission line...

  2. Determination of Metals Present in Textile Dyes Using Laser-Induced Breakdown Spectroscopy and Cross-Validation Using Inductively Coupled Plasma/Atomic Emission Spectroscopy

    Directory of Open Access Journals (Sweden)

    K. Rehan

    2017-01-01

    Full Text Available Laser-induced breakdown spectroscopy (LIBS was used for the quantitative analysis of elements present in textile dyes at ambient pressure via the fundamental mode (1064 nm of a Nd:YAG pulsed laser. Three samples were collected for this purpose. Spectra of textile dyes were acquired using an HR spectrometer (LIBS2000+, Ocean Optics, Inc. having an optical resolution of 0.06 nm in the spectral range of 200 to 720 nm. Toxic metals like Cr, Cu, Fe, Ni, and Zn along with other elements like Al, Mg, Ca, and Na were revealed to exist in the samples. The %-age concentrations of the detected elements were measured by means of standard calibration curve method, intensities of every emission from every species, and calibration-free (CF LIBS approach. Only Sample 3 was found to contain heavy metals like Cr, Cu, and Ni above the prescribed limit. The results using LIBS were found to be in good agreement when compared to outcomes of inductively coupled plasma/atomic emission spectroscopy (ICP/AES.

  3. Volcanic SO2 and SiF4 visualization and their ratio monitored using 2-D thermal emission spectroscopy

    Science.gov (United States)

    Stremme, W.; Krueger, A.; Harig, R.; Grutter, M.

    2011-09-01

    The composition and emission rates of volcanic gas plumes provide insight of the geologic internal activity, atmospheric chemistry, aerosol formation and radiative processes around it. Observations are necessary for public security and the aviation industry. Ground-based thermal emission infrared spectroscopy, which uses the radiation of the volcanic gas itself, allows for continuously monitoring during day and night from a save distance. We present measurements on Popocatépetl volcano based on thermal emission spectroscopy during different campaigns between 2006-2009 using a Scanning Infrared Gas Imaging System (SIGIS). The experimental set-up, measurement geometries and analytical algorithms are described. The equipment was operated from a safe distance of 12 km from the volcano at two different spectral resolutions: 0.5 and 4 cm-1. The 2-dimensional scanning capability of the instrument allows for an on-line visualization of the volcanic SO2 plume, animation and determination of its propagation speed. SiF4 was also identified in the infrared spectra recorded at both resolutions. The SiF4/SO2 molecular ratio can be calculated from each image and used as a highly useful parameter to follow changes in volcanic activity. A small Vulcanian eruption was monitored during the night of 16 to 17 November 2008 which was confirmed from the strong ash emission registered around 01:00 a.m. LST (Local Standard Time) and a pronounced SO2 cloud was registered. Enhanced SiF4/SO2 ratios were observed before and after the eruption. A validation of the results from thermal emission measurements with those from absorption spectra of the moon taken at the same time, as well as an error analysis, are presented. The inferred propagation speed from sequential imagees is used to calculate the emission rates at different distances from the crater.

  4. Analysis of whole blood samples with low gas flow inductively coupled plasma-optical emission spectrometry.

    Science.gov (United States)

    Nowak, Sascha; Künnemeyer, Jens; Terborg, Lydia; Trümpler, Stefan; Günsel, Andreas; Wiesmüller, Gerhard A; Karst, Uwe; Buscher, Wolfgang

    2015-01-01

    Low gas flow ICP-OES with a total argon consumption below 0.7 L/min is introduced for the analysis of trace elements in blood samples to investigate the influence of samples containing an organic solvent in a demanding matrix on the performance of this plasma for the first time. Therefore, gadolinium was determined in human plasma samples and mercury in red blood cells, human plasma, and precipitated plasma protein fraction. Limits of detection (LOD) were determined to be in the low microgram per liter range for the analytes and the accuracy of the method was assessed by comparison with a conventional Fassel-type torch-based ICP-OES. It was proven that the low gas flow ICP-OES leads to comparable results with the instrument based on the Fassel-type torch.

  5. Optical emission spectroscopy characterizations of micro-air plasma used for simulation of cell membrane poration

    Science.gov (United States)

    Zerrouki, A.; Motomura, H.; Ikeda, Y.; Jinno, M.; Yousfi, M.

    2016-07-01

    A micro-air corona discharge, which is one of the plasmas successfully used for gene transfection in terms of high transfection and cell viability rates, is characterized by optical emission spectroscopy. This non-equilibrium low temperature plasma is generated from the tip of a pulsed high voltage micro-tube (0.2 mm inner diameter and 0.7 mm for outer diameter) placed 2 mm in front of a petri dish containing deionized water and set on a grounded copper plate. The electron temperature, equal to about 6.75 eV near the electrode tip and decreased down to 3.4 eV near the plate, has been estimated, with an error bar of about 30%, from an interesting approach based on the experimental ratio of the closest nitrogen emission spectra of \\text{N}2+ (FNS) at 391.4 nm and N2(SPS) at 394.3 nm. This is based on one hand on a balance equation between creations and losses of the excited upper levels of these two UV spectra and on the other hand on the electron impact rates of the creation of these upper levels calculated from solution of the multi-term Boltzmann equation. Then using the measured Hα spectrum, electron density n e has been estimated from Stark broadening versus the inter-electrode position with an average error bar of about 50%. n e  ≈  1  ×  1015 cm-3 is near the tip coherent with the usual magnitude of electron density in the streamer head developed near the tip of the corona discharges. Rotational temperatures, estimated from comparison of synthetic and experimental spectra of OH(A  -  X), \\text{N}2+ (FNS) at 391.4 nm, and N2(SPS) at 337 nm are respectively equal to 2350 K, 2000 K and 700 K in the gap space. This clearly underlines a thermal non-equilibrium of the corresponding excited species generated inside the thin streamer filaments. But, due to the high dilution of these species in the background gas, these high rotational temperatures do not affect the mean gas temperature that remains close to 300

  6. Multi-epoch Spectroscopy of Dwarf Galaxies with AGN Signatures: Identifying Sources with Persistent Broad H-alpha Emission

    CERN Document Server

    Baldassare, Vivienne F; Gallo, Elena; Greene, Jenny E; Graur, Or; Geha, Marla; Hainline, Kevin; Carroll, Christopher M; Hickox, Ryan C

    2016-01-01

    We use time-domain optical spectroscopy to distinguish between broad emission lines powered by accreting black holes (BHs) or stellar processes (i.e., supernovae) for 16 galaxies identified as AGN candidates by Reines et al. (2013). 14 of these have star-formation--dominated narrow-line emission ratios, one is a narrow-line AGN, and the last is a star-forming--AGN composite. We find that broad H$\\alpha$ emission has faded for 11/16 targets, based on spectra taken with the Magellan Echellette Spectrograph (MagE), the Dual Imaging Spectrograph, and the Ohio State Multi-Object Spectrograph with baselines ranging from 5 to 14 years. The 11 faded systems all have narrow-line ratios consistent with recent star formation, suggesting the broad emission for those targets was produced by a transient stellar process. The two objects with narrow-line AGN signatures (RGG 9 and RGG 119) have persistent broad H$\\alpha$ emission consistent with previous SDSS observations. The final three star-forming objects are classified a...

  7. Dynamics of double-pulse laser produced titanium plasma inferred from thin film morphology and optical emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Krstulović, N., E-mail: niksak@ifs.hr [Institute of Physics, Bijenička 46, HR-10000 Zagreb (Croatia); Salamon, K., E-mail: ksalamon@ifs.hr [Institute of Physics, Bijenička 46, HR-10000 Zagreb (Croatia); Modic, M., E-mail: martina.modic@ijs.si [Jožef Stefan Institute, Jamova 39, 1001 Ljubljana (Slovenia); Bišćan, M., E-mail: mbiscan@ifs.hr [Institute of Physics, Bijenička 46, HR-10000 Zagreb (Croatia); Milat, O., E-mail: milat@ifs.hr [Institute of Physics, Bijenička 46, HR-10000 Zagreb (Croatia); Milošević, S., E-mail: slobodan@ifs.hr [Institute of Physics, Bijenička 46, HR-10000 Zagreb (Croatia)

    2015-05-01

    In this paper, dynamics of double-pulse laser produced titanium plasma was studied both directly using optical emission spectroscopy (OES) and indirectly from morphological properties of deposited thin films. Both approaches yield consistent results. Ablated material was deposited in a form of thin film on the Si substrate. During deposition, plasma dynamics was monitored using optical emission spectroscopy with spatial and temporal resolutions. The influence of ablation mode (single and double) and delay time τ (delay between first and second pulses in double-pulse mode) on plasma dynamics and consequently on morphology of deposited Ti-films was studied using X-ray reflectivity and atomic force microscopy. Delay time τ was varied from 170 ns to 4 μs. The results show strong dependence of both emission signal and Ti-film properties, such as thickness, density and roughness, on τ. In addition, correlation of average density and thickness of film is observed. These results are discussed in terms of dependency of angular distribution and kinetic energy of plasma plume particles on τ. Advantages of using double-pulse laser deposition for possible application in thin film production are shown. - Highlights: • Ti-thin films produced by single and double pulse laser ablation mode. • Ablation mode and delay time influenced plasma plume and film characteristics. • Films are most compact for optimized delay time (thinnest, smoothest and most dense). • Plasma dynamics can be inferred from film characteristics.

  8. Optical Emission Spectroscopy Study of Competing Phases of Electrons in the Second Landau Level.

    Science.gov (United States)

    Levy, A L; Wurstbauer, U; Kuznetsova, Y Y; Pinczuk, A; Pfeiffer, L N; West, K W; Manfra, M J; Gardner, G C; Watson, J D

    2016-01-01

    Quantum phases of electrons in the filling factor range 2≤ν≤3 are probed by the weak optical emission from the partially populated second Landau level and spin wave measurements. Observations of optical emission include a multiplet of sharp peaks that exhibit a strong filling factor dependence. Spin wave measurements by resonant inelastic light scattering probe breaking of spin rotational invariance and are used to link this optical emission with collective phases of electrons. A remarkably rapid interplay between emission peak intensities manifests phase competition in the second Landau level.

  9. Electron energy-loss and soft X-ray emission spectroscopy of electronic structure of MgB4

    Science.gov (United States)

    Sato, Yohei; Saito, Taiki; Tsuchiya, Kohei; Terauchi, Masami; Saito, Hiroki; Takeda, Masatoshi

    2017-09-01

    The electronic structure of MgB4, with the characteristic crystal structure comprising one-dimensional pentagonal B6 cluster chain, was investigated using electron energy-loss spectroscopy and soft X-ray emission spectroscopy based on transmission electron microscopy. The dielectric function and density of state of unoccupied and occupied states were clarified experimentally for the first time. Although theoretical calculations has predicted MgB4 to be a semiconductor, the electron energy-loss spectrum in this study show a plasmon peak at 0.4 eV, which might be due to carrier electrons. Theoretical calculations suggested that the electronic states near the Fermi energy are localized along the one dimensional B6 cluster chain. Therefore, one-dimensional electric conductivity is expected.

  10. OPEN PATH TUNABLE DIODE LASER ABSORPTION SPECTROSCOPY FOR ACQUISITION OF FUGITIVE EMISSION FLUX DATA

    Science.gov (United States)

    Air pollutant emission from unconfined sources is an increasingly important environmental issue. The U.S. EPA has developed a gorund-based optical remote sensing method that enables direct measurement of fugitive emission flux from large area sources. Open-path Fourier transfor...

  11. Effect of Surface Hydrogen Coverage on Field Emission Properties of DiamondFilms Investigated by High-Resolution Electron Energy Loss Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    WANG Yu-Guang; XIONG Yan-Yun; LIN Zhang-Da; FENG Ke-An; GU Chang-Zhi; JIN Zeng-Sun

    2000-01-01

    The influence of surface hydrogen coverage on the electron field emission of diamond films was investigated by high-resolution electron energy loss spectroscopy. It was found that hydrogen plasma treatment increased the surface hydrogen coverage while annealing caused hydrogen desorption and induced surface reconstruction. Field electron emission measurements manifested that increase of surface hydrogen coverage could improve the field emission properties, due to the decrease of electron affinity of the diamond .surface hy hvdrogen adsorption.

  12. Emission Spectroscopy of the 4X Source Discharge With and Without N2 Gas

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Horace Vernon [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-01-14

    This tech note summarizes the December, 1988 emission spectroscopy measurements made on the 4X source discharge with and without N₂ gas added to the H + Cs discharge. This study is motivated by the desire to understand why small amounts of N₂ gas added to the source discharge results in a reduction in the H⁻ beam noise. The beneficial effect of N₂ gas on H⁻ beam noise was first discovered by Bill Ingalls and Stu Orbesen on the ATS SAS source. For the 4X source the observed effect is that when N2 gas is added to the discharge the H⁻ beam noise is reduced about a factor of 2.

  13. Radio imaging spectroscopy of synchrotron emission associated with a CME on the 14th of August 2010

    Science.gov (United States)

    Bain, Hazel; Krucker, S.; Saint-Hilaire, P.; Raftery, C.

    2013-07-01

    We present Nancay Radioheliograph observations of a moving type IV solar radio burst which occurred in association with a CME on the 14th of August 2010. The event was well observed at extreme ultraviolet wavelengths by the Atmospheric Imaging Assembly onboard the Solar Dynamics Observatory, the SWAP instrument onboard Proba2 and by the LASCO white light coronograph. The burst emission was found to be cospatial with the core of the CME. Using radio imaging spectroscopy we are able to characterize the underlying electron distribution and plasma parameters within the source. Fitted spectra reveal a clear power law component consistent with optically thin synchrotron emission from accelerated electrons trapped in the erupting flux rope. As is often observed in type IV bursts, polarization measurements show the source to be moderately polarized during the peak of the burst, before steadily increasing to around 70% as the brightness temperature of the burst decays.

  14. Investigation of the atomic emission spectroscopy of F atoms and CF2 molecules in CF4 plasma processing

    Science.gov (United States)

    Jin, Huiliang; Li, Jie; Tang, Caixue; Deng, Wenhui; Chen, Xianhua

    2016-10-01

    The surface chemistry reaction involved in the processing of Atmospheric Pressure Plasma Jet (APPJ) produced from CF4 precursor has been explored. The atomic emission spectroscopy of F atoms and CF2 molecules was investigated as they contribute to substrate etching and FC film formation during APPJ processing. Optical emission spectroscopy (OES) spectra were acquired for CF4 plasma, relative concentrations of excited state species of F atoms and CF2 molecules were also dependent upon plasma parameters. The densities of F atoms increased dramatically with increasing applied RF power, whereas CF2 molecules decreased monotonically over the same power range, the subsequent electron impacted decomposition of plasma species after CF4 precursor fragmentation. The spectrum of the F atoms and CF2 molecules fallowed the same tendency with the increasing concentration of gas CF4, reaching the maximum at the 20sccm and 15sccm respectively, and then the emission intensity of reactive atoms decreased with more CF4 molecules participating. Addition certain amount O2 into CF4 plasma resulted in promoting CF4 dissociation, O2 can easily react with the dissociation product of CF2 molecules, which inhibit the compound of the F atoms, so with the increasing concentration of O2, the concentration of the CF2 molecules decreased and the emission intensities of F atoms showed the maximum at the O2/CF4 ratio of 20%. These results have led to the development of a scheme that illustrates the mechanisms of surface chemistry reaction and the affection of plasma parameters in CF4 plasma systems with respect to F and CF2 gas-phase species.

  15. X-ray continuum emission spectroscopy from hot dense matter at Gbar pressures

    Energy Technology Data Exchange (ETDEWEB)

    Kraus, D., E-mail: dominik.kraus@berkeley.edu; Falcone, R. W. [Department of Physics, University of California, Berkeley, California 94720 (United States); Döppner, T.; Kritcher, A. L.; Bachmann, B.; Collins, G. W.; Hawreliak, J. A.; Landen, O. L.; Ma, T.; Le Pape, S.; Swift, D. C. [Lawrence Livermore National Laboratory, Livermore, California 94550 (United States); Chapman, D. A. [Plasma Physics Group, Radiation Physics Department, AWE plc, Reading RG7 4PR, United Kingdom and Centre for Fusion, Space and Astrophysics, University of Warwick, Coventry CV4 7AL (United Kingdom); Glenzer, S. H. [SLAC National Accelerator Laboratory, Menlo Park, California 94309 (United States); Neumayer, P. [GSI Helmholtzzentrum für Schwerionenforschung, 64291 Darmstadt (Germany)

    2014-11-15

    We have measured the time-resolved x-ray continuum emission spectrum of ∼30 times compressed polystyrene created at stagnation of spherically convergent shock waves within the Gbar fundamental science campaign at the National Ignition Facility. From an exponential emission slope between 7.7 keV and 8.1 keV photon energy and using an emission model which accounts for reabsorption, we infer an average electron temperature of 375 ± 21 eV, which is in good agreement with HYDRA-1D simulations.

  16. Evidence of satellite valley position in GaN by photoexcited field emission spectroscopy

    Science.gov (United States)

    Yilmazoglu, O.; Pavlidis, D.; Hartnagel, H. L.; Evtukh, A.; Litovchenko, V.; Semenenko, N.

    2008-06-01

    GaN field emitter rods with nanometer diameter were fabricated by photoelectrochemical etching on a n+-GaN substrate. Their electron field emission properties were investigated under ultraviolet (UV) illumination. The Fowler-Nordheim plots of the emission current show different slopes for nonilluminated and UV illuminated devices. A model based on the electron emission from valleys having different specific electron affinities is proposed to explain the experimental results. In the absence of illumination, the GaN rods are almost fully depleted and emission takes place only from the lower valley. Upon UV illumination and presence of a high electric field at the emitter tip, the upper valley of the conduction band appears to be occupied by electrons generated at the valence band. The energy difference between the lower and upper valleys was determined to be 1.15eV and is in good agreement with formerly published theoretical and measured values.

  17. Flash Spectroscopy: Emission Lines from the Ionized Circumstellar Material around $<10$-Day-Old Type II Supernovae

    CERN Document Server

    Khazov, D; Gal-Yam, A; Manulis, I; Rubin, A; Kulkarni, S R; Arcavi, I; Kasliwal, M M; Ofek, E O; Cao, Y; Perley, D; Sollerman, J; Horesh, A; Sullivan, M; Filippenko, A V; Nugent, P E; Howell, D A; Cenko, S B; Silverman, J M; Ebeling, H; Taddia, F; Johansson, J; Laher, R R; Surace, J; Rebbapragada, U D; Wozniak, P R; Matheson, T

    2015-01-01

    Supernovae (SNe) embedded in dense circumstellar material (CSM) may show prominent emission lines in their early-time spectra ($\\leq 10$ days after the explosion), owing to recombination of the CSM ionized by the shock-breakout flash. From such spectra ("flash spectroscopy"), we can measure various physical properties of the CSM, as well as the mass-loss rate of the progenitor during the year prior to its explosion. Searching through the Palomar Transient Factory (PTF and iPTF) SN spectroscopy databases from 2009 through 2014, we found 12 Type II SNe showing flash-ionized (FI) signatures in their first spectra. All are younger than 10 days. These events constitute 14\\% of all 84 SNe in our sample having a spectrum within 10 days from explosion, and 18\\% of SNe~II observed at ages $<5$ days, thereby setting lower limits on the fraction of FI events. We classified as "blue/featureless" (BF) those events having a first spectrum which is similar to that of a black body, without any emission or absorption signa...

  18. Characterization of RF He-N2/Ar mixture plasma via Langmuir probe and optical emission spectroscopy techniques

    Science.gov (United States)

    Younus, Maria; Rehman, N. U.; Shafiq, M.; Hussain, S. S.; Zakaullah, M.; Zaka-ul-Islam, M.

    2016-08-01

    A Magnetic Pole Enhanced inductively coupled RF H e - N 2 / A r plasma is characterized using a Langmuir probe and optical emission spectroscopy (OES) techniques. The effect of helium mixing on electron density ( n e ) and temperature ( T e ) , electron energy probability functions (EEPFs), [ N ] atomic density, and N 2 dissociation is investigated. A Langmuir probe and a zero slope method based on trace rare gas-optical emission spectroscopy (TRG-OES) are employed to measure the electron temperature. It is noted that the electron temperature shows an increasing trend for both methods. However, the temperature measured by a zero slope method T e ( Z . S ) approaches the temperature measured by a Langmuir probe; T e ( L . P ) at 56% and above helium concentration in the discharge. "Advance actinometry" is employed to monitor the variation in [ N ] atomic density with helium concentration and gas pressure. It is noted that [ N ] atomic density increases at 56% and above helium in the discharge, which is consistent with the trend of electron temperature and EEPFs. A drastic enhancement in N 2 dissociation fraction D 1 determined by "advance actinometry" is noted at 56% and above helium concentration in the mixture due to modifications in different population and depopulation mechanisms. However, it is also noted that the dissociation fraction D 2 determined by intensity ratio method increases linearly with helium addition.

  19. The Development of Cavity Ringdown Spectroscopy as a Toxic Metal Continuous Emission Monitor

    Energy Technology Data Exchange (ETDEWEB)

    Dr. Goeroge P. Miller; Dr. Christopher B. Winstead

    2001-12-04

    Innovative program to explore the viability of using Cavity Ringdown Spectroscopy (CRDS) for trace analysis and monitoring of remediation processes for hazardous and radioactive wastes. Cavity ringdown spectroscopy is a measurement of the rate of absorption of a sample within a closed optical cavity rather than the standard measurement of the avsorved signal strength over a given sample path. It is a technique capable of providing ultra-sensitive absorption measurements in hostile environments using commercially available easy-to-use pulsed lasers. The inherent high sensitivity stems from both the long effective sample pathlengths possible and the relaxed constraints on the accuracy of the measurement of the cavity decay time.

  20. Time-resolved characterization of a filamentary argon discharge at atmospheric pressure in a capillary using emission and absorption spectroscopy

    Science.gov (United States)

    Schröter, Sandra; Pothiraja, Ramasamy; Awakowicz, Peter; Bibinov, Nikita; Böke, Marc; Niermann, Benedikt; Winter, Jörg

    2013-11-01

    An argon/nitrogen (0.999/0.001) filamentary pulsed discharge operated at atmospheric pressure in a quartz tube is characterized using voltage-current measurements, microphotography, optical emission spectroscopy (OES) and absorption spectroscopy. Nitrogen is applied as a sensor gas for the purpose of OES diagnostic. The density of argon metastable atoms Ar(3P2) is determined using tunable diode laser absorption spectroscopy (TDLAS). Using a plasma chemical model the measured OES data are applied for the characterization of the plasma conditions. Between intense positive pulses the discharge current oscillates with a damped amplitude. It is established that an electric current flows in this discharge not only through a thin plasma filament that is observed in the discharge image but also through the whole cross section of the quartz tube. A diffuse plasma fills the quartz tube during a time between intense current pulses. Ionization waves are propagating in this plasma between the spike and the grounded area of the tube producing thin plasma channels. The diameter of these channels increases during the pause between the propagation of ionization waves probably because of thermal expansion and diffusion. Inside the channels electron densities of ˜2 × 1013 cm-3, argon metastable densities ˜1014 cm-3 and a reduced electric field about 10 Td are determined.

  1. UVES and X-Shooter spectroscopy of the emission line AM CVn systems GP Com and V396 Hya

    Science.gov (United States)

    Kupfer, T.; Steeghs, D.; Groot, P. J.; Marsh, T. R.; Nelemans, G.; Roelofs, G. H. A.

    2016-04-01

    We present time-resolved spectroscopy of the AM CVn-type binaries GP Com and V396 Hya obtained with VLT/X-Shooter and VLT/UV-Visual Echelle Spectrograph (UVES). We fully resolve the narrow central components of the dominant helium lines and determine radial velocity semi-amplitudes of Kspike = 11.7 ± 0.3 km s-1 for GP Com and Kspike = 5.8 ± 0.3 km s-1 for V396 Hya. The mean velocities of the narrow central components show variations from line to line. Compared to calculated line profiles that include Stark broadening we are able to explain the displacements, and the appearance of forbidden helium lines, by additional Stark broadening of emission in a helium plasma with an electron density ne ≃ 5 × 1015 cm-3. More than 30 nitrogen and more than 10 neon lines emission lines were detected in both systems. Additionally, 20 nitrogen absorption lines are only seen in GP Com. The radial velocity variations of these lines show the same phase and velocity amplitude as the central helium emission components. The small semi-amplitude of the central helium emission component, the consistency of phase and amplitude with the absorption components in GP Com as well as the measured Stark effect shows that the central helium emission component, the so-called central-spike, is consistent with an origin on the accreting white dwarf. We use the dynamics of the bright spot and the central-spike to constrain the binary parameters for both systems and find a donor mass of 9.6-42.8 MJupiter for GP Com and 6.1-30.5 MJupiter for V396 Hya. We find an upper limit for the rotational velocity of the accretor of vrot < 46 km s-1 for GP Com and vrot < 59 km s-1 for V396 Hya which excludes a fast rotating accretor in both systems.

  2. Development of a new laboratory technique for high-temperature thermal emission spectroscopy of silicate melts

    Science.gov (United States)

    Lee, Rachel J.; Ramsey, Michael S.; King, Penelope L.

    2013-05-01

    the prevalence of glass and molten silicates in volcanic environments, and the important role of surface emissivity in thermal infrared (TIR) measurements, it is imperative to characterize accurately the spectral features associated with silicate glasses and melts. A microfurnace has been developed specifically for use with a laboratory Fourier transform infrared (FTIR) spectrometer to collect the first in situ TIR emission spectra of actively melting and cooling silicate glasses. The construction, implementation, and calibration of the microfurnace spectrometer system are presented here. Initial testing of the microfurnace is also discussed, which includes acquisition of thermal emission spectra of a quartz powder (unmelted), a melted and cooled oligoclase feldspar, and glassy melt of rhyolitic composition. Unlike a solid material, which may only have bending and stretching vibrations within its molecular structure, a fully molten material will exhibit several more degrees of freedom in structural movement, thus changing its spectral character. Differences in spectral behavior and morphology are observed between a glass in a solid state and its molten counterpart, confirming previous field measurements of lower emissivity upon melting. This laboratory microfurnace system has been designed to quantify the TIR emission spectral behavior of glassy materials in various physical states. Ultimately, it is hoped that the microfurnace data will help improve the ability of field-based, airborne, and spaceborne TIR data to characterize glassy volcanic terranes.

  3. Optical emission spectroscopy of point-plane corona and back-corona discharges in air

    Science.gov (United States)

    Czech, T.; Sobczyk, A. T.; Jaworek, A.

    2011-12-01

    Results of spectroscopic investigations and current-voltage characteristics of corona discharge and back discharge on fly-ash layer, generated in point-plane electrode geometry in air at atmospheric pressure are presented in the paper. The characteristics of both discharges are similar but differ in the current and voltage ranges of all the discharge forms distinguished during the experiments. Three forms of back discharge, for positive and negative polarity, were investigated: glow, streamer and low-current back-arc. In order to characterize ionisation and excitation processes in back discharge, the emission spectra were measured and compared with those obtained for normal corona discharge generated in the same electrode configuration but with fly ash layer removed. The emission spectra were measured in two discharge zones: near the tip of needle electrode and near the plate. Visual forms of the discharge were recorded with digital camera and referred to current-voltage characteristics and emission spectra. The measurements have shown that spectral lines emitted by back discharge depend on the form of discharge and the discharge current. From the comparison of the spectral lines of back and normal discharges an effect of fly ash layer on the discharge morphology can be determined. The recorded emission spectra formed by ionised gas and plasma near the needle electrode and fly ash layer are different. It should be noted that in back arc emission, spectral lines of fly ash layer components can be distinguished. On the other hand, in needle zone, the emission of high intensity N2 second positive system and NO γ lines can be noticed. Regardless of these gaseous lines, also atomic lines of dust layer were present in the spectrum. The differences in spectra of back discharge for positive and negative polarities of the needle electrode have been explained by considering the kind of ions generated in the crater in fly ash layer. The aim of these studies is to better

  4. The primary photophysics of the Avena sativa phototropin 1 LOV2 domain observed with time-resolved emission spectroscopy.

    Science.gov (United States)

    van Stokkum, Ivo H M; Gauden, Magdalena; Crosson, Sean; van Grondelle, Rienk; Moffat, Keith; Kennis, John T M

    2011-01-01

    The phototropins are blue-light receptors that base their light-dependent action on the reversible formation of a covalent bond between a flavin mononucleotide (FMN) cofactor and a conserved cysteine in light, oxygen or voltage (LOV) domains. The primary reactions of the Avena sativa phototropin 1 LOV2 domain were investigated by means of time-resolved and low-temperature fluorescence spectroscopy. Synchroscan streak camera experiments revealed a fluorescence lifetime of 2.2 ns in LOV2. A weak long-lived component with emission intensity from 600 to 650 nm was assigned to phosphorescence from the reactive FMN triplet state. This observation allowed determination of the LOV2 triplet state energy level at physiological temperature at 16600 cm(-1). FMN dissolved in aqueous solution showed pH-dependent fluorescence lifetimes of 2.7 ns at pH 2 and 3.9-4.1 ns at pH 3-8. Here, too, a weak phosphorescence band was observed. The fluorescence quantum yield of LOV2 increased from 0.13 to 0.41 upon cooling the sample from 293 to 77 K. A pronounced phosphorescence emission around 600 nm was observed in the LOV2 domain between 77 and 120 K in the steady-state emission.

  5. Using an artificial neural network to classify multicomponent emission lines with integral field spectroscopy from SAMI and S7

    Science.gov (United States)

    Hampton, E. J.; Medling, A. M.; Groves, B.; Kewley, L.; Dopita, M.; Davies, R.; Ho, I.-T.; Kaasinen, M.; Leslie, S.; Sharp, R.; Sweet, S. M.; Thomas, A. D.; Allen, J.; Bland-Hawthorn, J.; Brough, S.; Bryant, J. J.; Croom, S.; Goodwin, M.; Green, A.; Konstantantopoulos, I. S.; Lawrence, J.; López-Sánchez, Á. R.; Lorente, N. P. F.; McElroy, R.; Owers, M. S.; Richards, S. N.; Shastri, P.

    2017-09-01

    Integral field spectroscopy (IFS) surveys are changing how we study galaxies and are creating vastly more spectroscopic data available than before. The large number of resulting spectra makes visual inspection of emission line fits an infeasible option. Here, we present a demonstration of an artificial neural network (ANN) that determines the number of Gaussian components needed to describe the complex emission line velocity structures observed in galaxies after being fit with lzifu. We apply our ANN to IFS data for the S7 survey, conducted using the Wide Field Spectrograph on the ANU 2.3 m Telescope, and the SAMI Galaxy Survey, conducted using the SAMI instrument on the 4 m Anglo-Australian Telescope. We use the spectral fitting code lzifu (Ho et al. 2016a) to fit the emission line spectra of individual spaxels from S7 and SAMI data cubes with 1-, 2- and 3-Gaussian components. We demonstrate that using an ANN is comparable to astronomers performing the same visual inspection task of determining the best number of Gaussian components to describe the physical processes in galaxies. The advantage of our ANN is that it is capable of processing the spectra for thousands of galaxies in minutes, as compared to the years this task would take individual astronomers to complete by visual inspection.

  6. UVES and X-Shooter spectroscopy of the emission line AM CVn systems GP Com and V396 Hya

    CERN Document Server

    Kupfer, T; Groot, P J; Marsh, T R; Nelemans, G; Roelofs, G H A

    2016-01-01

    We present time-resolved spectroscopy of the AM CVn-type binaries GP Com and V396 Hya obtained with VLT/X-Shooter and VLT/UVES. We fully resolve the narrow central components of the dominant helium lines and determine radial velocity semi-amplitudes of $K_{\\rm spike} = 11.7\\pm0.3$ km s$^{-1}$ for GP Com and $K_{\\rm spike} = 5.8\\pm0.3$ km s$^{-1}$ for V396 Hya. The mean velocities of the narrow central components show variations from line to line. Compared to calculated line profiles that include Stark broadening we are able to explain the displacements, and the appearance of forbidden helium lines, by additional Stark broadening of emission in a helium plasma with an electron density $n_e\\simeq 5\\times 10^{15}$ cm$^{-3}$. More than $30$ nitrogen and more than $10$ neon lines emission lines were detected in both systems. Additionally, $20$ nitrogen absorption lines are only seen in GP Com. The radial velocity variations of these lines show the same phase and velocity amplitude as the central helium emission co...

  7. Cobalt(II) complexation with small biomolecules as studied by 57Co emission Mössbauer spectroscopy

    Science.gov (United States)

    Kamnev, Alexander A.; Perfiliev, Yurii D.; Kulikov, Leonid A.; Tugarova, Anna V.; Kovács, Krisztina; Homonnay, Zoltán; Kuzmann, Ernő

    2017-02-01

    In the emission (57Co) variant of Mössbauer spectroscopy (EMS), the 57Co radionuclide (with a half-life of 9 months) is used that undergoes a nuclear decay 57Co → 57Fe via electron capture followed by the emission of a γ-quantum, the energy of which is modified by the chemical state and the close coordination environment of the parent 57Co atom. While EMS has been used largely in materials science and nuclear chemistry, its high sensitivity can also be of great advantage in revealing fine structural features and for speciation analysis of biological complexes, whenever the 57Co2 + cation can be used directly as the coordinating metal or as a substitute for native cobalt or other metal ions. As such EMS applications are yet rare, in order to reliably interpret emission spectra of sophisticated 57Co2 +-doped biosystems, model EMS studies of simple cobalt biocomplexes are necessary. In this work, EMS spectroscopic data are analysed and discussed for 57Co2 + complexes with a range of small biomolecules of different structures, including 4-n-hexylresorcinol, homoserine lactone and a few amino acids (spectra measured in rapidly frozen dilute aqueous solutions or in the dried state at T = 80 K). The EMS data obtained are discussed with regard to the available literature data related to the coordination modes of the biocomplexes under study.

  8. Emission Mössbauer spectroscopy of advanced materials for opto- and nano-electronics

    CERN Multimedia

    Olafsson, S; Weyer, G O P; Masenda, H; Dlamini, W B

    Mössbauer Spectroscopy (MS) is a versatile solid state method giving information about probe atom interactions with its nearest neighbours. Simultaneously, information on the probe valence state, site symmetry, and electric and magnetic hyperfine interactions is obtained. MS can be applied in many different contexts in material science and solid state physics. MS using radioactive isotopes, applied for decades at the ISOLDE facilities, has the particular merit of very high sensitivity. This opens up many new possibilities compared to traditional (absorption) Mössbauer spectroscopy. Among them is the possibility of working with very low concentrations (10$^{-4}$ at. ~\\%), where the probe atoms are true dilute impurities. Here we propose four main themes in our Mössbauer investigations for the coming years: \\\\(1) Para-magnetic relaxations in compound semiconductors. \\\\(2) Vacancy diffusion in group IV semiconductors. \\\\(3) Doping of Si-nano-particles. \\\\(4) Investigation of phase change mechanisms in chalcog...

  9. Excitation-emission fluorescence spectroscopy and time-gated Raman microscopy analysis of dental tissues

    Science.gov (United States)

    Mukhin, M.; Sen, S.; Kouklin, Nikolai A.; Skliarov, A.; Dhuru, D. B.; Iacopino, A. M.; Yakovlev, Vladislav V.

    2007-02-01

    We applied two new spectroscopic techniques (time-gated Raman microscopy and excitation-emission fluorescence microspectroscopy) to characterize healthy and carious dental tissues. These methods were used together with visual inspection, DIAGNOdent, optical polarization microscopy, scanning electron microscopy, and chemical microanalysis to get a more detailed picture of chemical and structural transformations in dental tissues as a result of caries development.

  10. Remote measurement of high preeruptive water vapor emissions at Sabancaya volcano by passive differential optical absorption spectroscopy

    Science.gov (United States)

    Kern, Christoph; Masias, Pablo; Apaza, Fredy; Reath, Kevin; Platt, Ulrich

    2017-01-01

    Water (H2O) is by far the most abundant volcanic volatile species and plays a predominant role in driving volcanic eruptions. However, numerous difficulties associated with making accurate measurements of water vapor in volcanic plumes have limited their use as a diagnostic tool. Here we present the first detection of water vapor in a volcanic plume using passive visible-light differential optical absorption spectroscopy (DOAS). Ultraviolet and visible-light DOAS measurements were made on 21 May 2016 at Sabancaya Volcano, Peru. We find that Sabancaya's plume contained an exceptionally high relative water vapor abundance 6 months prior to its November 2016 eruption. Our measurements yielded average sulfur dioxide (SO2) emission rates of 800–900 t/d, H2O emission rates of around 250,000 t/d, and an H2O/SO2 molecular ratio of 1000 which is about an order of magnitude larger than typically found in high-temperature volcanic gases. We attribute the high water vapor emissions to a boiling-off of Sabancaya's hydrothermal system caused by intrusion of magma to shallow depths. This hypothesis is supported by a significant increase in the thermal output of the volcanic edifice detected in infrared satellite imagery leading up to and after our measurements. Though the measurement conditions encountered at Sabancaya were very favorable for our experiment, we show that visible-light DOAS systems could be used to measure water vapor emissions at numerous other high-elevation volcanoes. Such measurements would provide observatories with additional information particularly useful for forecasting eruptions at volcanoes harboring significant hydrothermal systems.

  11. Measuring one-dimensional and two-dimensional impurity density profiles on TEXTOR using combined charge exchange-beam emission spectroscopy and ultrasoft x-ray tomography

    Science.gov (United States)

    De Bock, M.; Jakubowska, K.; Hellermann, M. von; Jaspers, R.; Donné, A. J. H.; Shmaenok, L.

    2004-10-01

    Two techniques are presented that allow us to measure impurity density profiles in the TEXTOR tokamak plasma. The one-dimensional profiles are gathered by charge exchange recombination spectroscopy (CXRS) in combination with beam emission spectroscopy (BES). Combining CXRS and BES eliminate the need for absolute calibration. For two-dimensional profiles an ultrasoft x-ray tomography system has been developed. The system is spectrally resolved and produces local emissivity profiles of several ionization stages of impurities. Both systems are presently being commissioned. They are complementary and give an insight into the impurity distribution and transport in plasmas.

  12. The SMARTS Multi-epoch Optical Spectroscopy Atlas (SAMOSA): Using Emission Line Variability to Probe the Location of the Blazar Gamma-emitting Region

    CERN Document Server

    Isler, Jedidah C; Bailyn, C; Smith, P S; Coppi, P; Brady, M; Macpherson, E; Hasan, I; Buxton, M

    2015-01-01

    We present multi-epoch optical spectroscopy of seven southern Fermi-monitored blazars from 2008 - 2013 using the Small and Medium Aperture Research Telescope System (SMARTS), with supplemental spectroscopy and polarization data from the Steward Observatory. We find that the emission lines are much less variable than the continuum; 4 of 7 blazars had no detectable emission line variability over the 5 years. This is consistent with photoionization primarily by an accretion disk, allowing us to use the lines as a probe of disk activity. Comparing optical emission line flux with Fermi $\\gamma$-ray flux and optical polarized flux, we investigate whether relativistic jet variability is related to the accretion flow. In general, we see no such dependence, suggesting the jet variability is likely caused by internal processes like turbulence or shock acceleration rather than a variable accretion rate. However, three sources showed statistically significant emission line flares in close temporal proximity to very large...

  13. Tissue differentiation by means of high resolution optical emission spectroscopy during electrosurgical intervention

    Science.gov (United States)

    Bürger, Ines; Scharpf, Marcus; Hennenlotter, Jörg; Nüßle, Daniela; Spether, Dominik; Neugebauer, Alexander; Bibinov, Nikita; Stenzl, Arnulf; Fend, Falko; Enderle, Markus; Awakowicz, Peter

    2017-01-01

    Electrosurgery is the use of radio-frequency electric current for the cutting of biological tissue e.g. for resection of tumour tissue. In this work, the optical emission of plasma being generated during the electrosurgical procedure is investigated with a high resolution echelle spectrometer to find differences between tumour tissue and normal renal tissue in a pre-clinical ex vivo study. Trace elements like zinc, iron, copper and cadmium are present in the tissue spectra as well as the electrolytes magnesium, calcium, sodium and potassium and some diatomic molecules such as hydroxyl radical, cyano radical, dicarbon, nitrogen monohydride and molecular nitrogen which are mainly dissociated from polyatomic molecules. With the atomic emission line of cadmium at 228.8 nm the treated tissue can be differentiated in tumorous and healthy tissue with correct assignment of 95% for tumour tissue and 92% for normal renal tissue.

  14. [Study of a wire-to-plate positive pulsed corona discharge reactor by emission spectroscopy].

    Science.gov (United States)

    Wang, Shen-Bing; Luo, Zhong-Yang; Zhao, Lei; Xuan, Jian-Yong; Jiang, Jian-Ping; Cen, Ke-Fa

    2011-11-01

    In order to get extensive knowledge of wire-to-plate pulsed corona discharge reactor, the influences of different diameters of wire electrode, different wire-to-plate and wire-to-wire spacing on OH radical generation were experimentally investigated under atmospheric pressure based on emission spectrum, and the spatial distribution of OH radicals in the electric field was also discussed in detail The results showed that OH radicals decrease along the X-axis, and the activation radius is approximately 20 mm; showing a trend of first increase and then decrease along the Y-axis, with the activation radius being more than 30 mm. OH radical has small change as the diameter of wire electrode changes below 2 mm, with a sharp decline as the diameter continues to increase. OH radical emission intensity increases as wire-to-wire spacing increases and decrease as wire-to-plate spacing increases.

  15. VUV emission spectroscopy diagnostics of a 14 GHz ECR negative hydrogen ion source

    Science.gov (United States)

    Tamura, R.; Ichikawa, T.; Kasuya, T.; Nishiura, M.; Shimozuma, T.; Wada, M.

    2015-04-01

    Vacuum Ultra Violet(VUV) emission from a 4 cm diameter 2 cm long compact ion source excited by 14 GHz microwave has been investigated. Intensity ratio of band spectrum emission near Ly-α to Ly-α line spectrum is determined from the measured spectrum. which shows preferential excitation of molecules near the entrance of microwave input power. The ratio does not depend strongly upon pressure nor the input microwave power when the intensity is integrated over the volume of the plasma. The spatial distribution of the spectrum intensity ratio exhibits concentrations near microwave inlet and the opposite side where the microwave matching structure is located. The ratio at these peripheral regions is about two times as high as that of the central region. The ratio increased in proportion to the ion source pressure up to about 3.0 Pa, indicating efficient production of high energy electrons by ECR up to this pressure.

  16. Multireference X-Ray Emission and Absorption Spectroscopy calculations from Monte Carlo Configuration Interaction

    CERN Document Server

    Coe, J P

    2015-01-01

    We adapt the method of Monte Carlo configuration interaction to calculate core-hole states and use this for the computation of X-ray emission and absorption values. We consider CO, CH$_{4}$, NH$_{3}$, H$_{2}$O, HF, HCN, CH$_{3}$OH, CH$_{3}$F, HCl and NO using a 6-311G** basis. We also look at carbon monoxide with a stretched geometry and discuss the dependence of its results on the cutoff used. The Monte Carlo configuration interaction results are compared with EOM-CCSD values for X-ray emission and with experiment for X-ray absorption. Oscillator strengths are also computed and we quantify the multireference nature of the wavefunctions to suggest when approaches based on a single reference would be expected to be successful.

  17. X-ray Absorption and Emission Spectroscopy of the Intergalactic Medium at Small Redshift

    Science.gov (United States)

    Paerels, F.; Rasmussen, A.; Kahn, S.; Herder, J. W.; Vries, C.

    Recent observations with Chandra and XMM-Newton have begun to probe the properties of the intergalactic medium (IGM) at small redshifts. We briefly present a recent new result on resonance absorption by highly ionized oxygen at z ≈ 0 with the Reflection Grating Spectrometer on XMM-Newton, and then discuss the prospects for detecting line emission from the Warm-Hot phase of the IGM.

  18. Development of a Reference Database for Particle-Induced Gamma-ray Emission spectroscopy

    OpenAIRE

    Dimitriou, P.; Becker, H.-W.; Bogdanović-Radović, I.; M. Chiari; Goncharov, A.; Jesus, A. P.; Kakuee, O.; Kiss, A. Z.; Lagoyannis, A.; Räisänen, J.; Strivay, David; Zucchiatti, A.

    2016-01-01

    Particle-Induced Gamma-ray Emission (PIGE) is a powerful analytical technique that exploits the interactions of rapid charged particles with nuclei located near a sample surface to determine the composition and structure of the surface regions of solids by measurement of characteristic prompt γ rays. The potential for depth profiling of this technique has long been recognized, however, the implementation has been limited owing to insufficient knowledge of the physical data and lack of suitabl...

  19. No Evidence for Lyman-alpha Emission in Spectroscopy of z > 7 Candidate Galaxies

    CERN Document Server

    Caruana, Joseph; Wilkins, Stephen M; Stanway, Elizabeth R; Lacy, Mark; Jarvis, Matt J; Lorenzoni, Silvio; Hickey, Samantha

    2012-01-01

    We present Gemini/GNIRS spectroscopic observations of 4 z-band (z~7) dropout galaxies and VLT/XSHOOTER observations of one z-band dropout and 3 Y-band (z~8-9) dropout galaxies in the Hubble Ultra Deep Field, which were selected with Wide Field Camera 3 imaging on the Hubble Space Telescope. We find no evidence of Lyman-alpha emission with a typical 5-sigma sensitivity of 5X10^-18erg/cm^2/s, and we use the upper limits on Lyman-alpha flux and the broad-band magnitudes to constrain the rest-frame equivalent widths for this line emission. Accounting for incomplete spectral coverage, we survey 3.0 z-band dropouts and 2.9 Y-band dropouts to a Lyman-alpha rest-frame equivalent width limit > 120Ang (for an unresolved emission line); for an equivalent width limit of 50Ang the effective numbers of drop-outs surveyed fall to 1.2 z-band drop-outs and 1.5 Y-band drop-outs. A simple model where the fraction of high rest-frame equivalent width emitters follows the trend seen at z=3-6.5 is inconsistent with our non-detectio...

  20. Measurements of fluoride emissions in aluminum smelters by tunable diode laser spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Schiff, H.; Pisano, J.; Chanda, A.; Karecki, D.; Mackay, G.

    1999-07-01

    Tunable Diode Laser Absorption Spectrometry (TDLAS) is an effective method for measuring the emissions of fluoride compounds from primary aluminum production. Hydrogen fluoride is a highly toxic substance, harmful to both human health and the environment. The perfluorocarbons, CF{sub 4} and C{sub 2}F{sub 6}, are strong greenhouse gases with atmospheric lifetimes of more than 5,000 years. The LasIR systems based on near infrared tunable diode lasers have been used to measure HF in stacks, on both sides of scrubbers and in the pot-rooms of the smelter. Examples of these measurements are presented. The perfluorocarbons have been measured with a mid infrared TDLAS system by continuous extraction into a multipath White cell. Earlier measurements by this method clearly revealed the factors, which govern perfluorocarbon emissions and have led to improvement in aluminum production technology. Recent measurements have shown that the use of these technologies does, in fact, result in appreciable reduction in the emissions of the perfluorocarbons. The examples given in this paper demonstrate the ability and versatility of TDLAS systems for providing reliable, interference-free measurements of important gases in a complex mixture and in hostile environments.

  1. IFU spectroscopy of 10 early-type galactic nuclei - III. Properties of the circumnuclear gas emission

    CERN Document Server

    Ricci, T V; Menezes, R B

    2015-01-01

    Many Early-type galaxies (ETG) have ionized gas emission in their centres that extends to scales of ~ 1kpc. The majority of such objects are classified as LINERs, but the nature of their ionizing source is still not clear. The kinematics associated with these gaseous structures usually shows deviations from a pure rotational motion due to non-gravitational effects or to non-axisymmetric potentials. This is the third of a series of papers that describes a sample of 10 nearby and massive ETG observed with the Gemini Multi-Object Spectrograph in Integral Field mode installed on the Gemini-South telescope. In paper II, we performed spectral synthesis to subtract the stellar components from the data cubes of the sample galaxies in order to study their nuclear spectra. Here, we analyse the circumnuclear gas emission (scales of ~ 100 pc) of the sample galaxies. Circumnuclear gas emission was detected in seven galaxies, all of them classified as LINERs. Pure gaseous discs are found in three galaxies. In two objects, ...

  2. IFU spectroscopy of 10 early type galactic nuclei: II - Nuclear emission line properties

    CERN Document Server

    Ricci, T V; Menezes, R B

    2014-01-01

    Although it is well known that massive galaxies have central black holes, most of them accreting at low Eddington ratios, many important questions still remain open. Among them, are the nature of the ionizing source, the characteristics and frequencies of the broad line region and of the dusty torus. We report observations of 10 early-type galactic nuclei, observed with the IFU/GMOS spectrograph on the Gemini South telescope, analysed with standard techniques for spectral treatment and compared with results obtained with principal component analysis Tomography (Paper I). We performed spectral synthesis of each spaxel of the data cubes and subtracted the stellar component from the original cube, leaving a data cube with emission lines only. The emission lines were decomposed in multi-Gaussian components. We show here that, for eight galaxies previously known to have emission lines, the narrow line region can be decomposed in two components with distinct line widths. In addition to this, broad H$\\alpha$ emissio...

  3. Measuring Organic Molecular Emission in Disks with Low Resolution Spitzer Spectroscopy

    CERN Document Server

    Teske, Johanna K; Carr, John S; Pascucci, Ilaria; Apai, Daniel; Henning, Thomas

    2011-01-01

    We explore the extent to which Spitzer IRS spectra taken at low spectral resolution can be used in quantitative studies of organic molecular emission from disks surrounding low mass young stars. We use Spitzer IRS spectra taken in both the high and low resolution modules for the same sources to investigate whether it is possible to define line indices that can measure trends in the strength of the molecular features in low resolution data. We find that trends in HCN emission strength seen in the high resolution data can be recovered in low resolution data. In examining the factors that influence the HCN emission strength, we find that the low resolution HCN flux is modestly correlated with stellar accretion rate and X-ray luminosity. Correlations of this kind are perhaps expected based on recent observational and theoretical studies of inner disk atmospheres. Our results demonstrate the potential of using the large number of low resolution disk spectra that reside in the Spitzer archive to study the factors t...

  4. Band Gap Energy of Chalcopyrite Thin Film Solar Cell Absorbers Determined by Soft X-Ray Emission and Absorption Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Bar, M.; Weinhardt, L.; Pookpanratana, S.; Heske, C.; Nishiwaki, S.; Shafarman, W.; Fuchs, O.; Blum, M.; Yang, W.; Denlinger, J.D.

    2008-05-11

    The chemical and electronic structure of high efficiency chalcopyrite thin film solar cell absorbers significantly differs between the surface and the bulk. While it is widely accepted that the absorber surface exhibits a Cu-poor surface phase with increased band gap (Eg), a direct access to the crucial information of the depth-dependency of Eg is still missing. In this paper, we demonstrate that a combination of x-ray emission and absorption spectroscopy allows a determination of Eg in the surface-near bulk and thus complements the established surface- and bulk-sensitive techniques of Eg determination. As an example, we discuss the determination of Eg for a Cu(In,Ga)Se2 absorber [(1.52 +- 0.20) eV].

  5. Emission Mössbauer spectroscopy study of fluence dependence of paramagnetic relaxation in Mn/Fe implanted ZnO

    Science.gov (United States)

    Masenda, H.; Geburt, S.; Bharuth-Ram, K.; Naidoo, D.; Gunnlaugsson, H. P.; Johnston, K.; Mantovan, R.; Mølholt, T. E.; Ncube, M.; Shayestehaminzadeh, S.; Gislason, H. P.; Langouche, G.; Ólafsson, S.; Ronning, C.

    2016-12-01

    Emission Mössbauer Spectroscopy following the implantation of radioactive precursor isotope 57Mn+ ( T 1/2= 1.5 min) into ZnO single crystals at ISOLDE/CERN shows that a large fraction of 57Fe atoms produced in the 57Mn beta decay is created as paramagnetic Fe3+ with relatively long spin-lattice relaxation times. Here we report on ZnO pre-implanted with 56Fe to fluences of 2×1013, 5×10 13 and 8 × 1013 ions/cm2 in order to investigate the dependence of the paramagnetic relaxation rate of Fe3+ on fluence. The spectra are dominated by magnetic features displaying paramagnetic relaxation effects. The extracted spin-lattice relaxation rates show a slight increase with increasing ion fluence at corresponding temperatures and the area fraction of Fe3+ at room temperature reaches a maximum contribution of 80(3)% in the studied fluence range.

  6. Electronic structure of multiferroic BiFeO3 by resonant soft-x-ray emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Higuchi, Tohru; Higuchi, T.; Liu, Y.-S.; Yao, P.; Glans, P.-A.; Guo, Jinghua; Chang, C.; Wu, Z.; Sakamoto, W.; Itoh, N.; Shimura, T.; Yogo, T.; Hattori, T.

    2008-07-11

    The electronic structure of multiferroic BiFeO{sub 3} has been studied using soft-X-ray emission spectroscopy. The fluorescence spectra exhibit that the valence band is mainly composed of O 2p state hybridized with Fe 3d state. The band gap corresponding to the energy separation between the top of the O 2p valence band and the bottom of the Fe 3d conduction band is 1.3 eV. The soft-X-ray Raman scattering reflects the features due to charge transfer transition from O 2p valence band to Fe 3d conduction band. These findings are similar to the result of electronic structure calculation by density functional theory within the local spin-density approximation that included the effect of Coulomb repulsion between localized d states.

  7. Non-gated laser induced breakdown spectroscopy provides a powerful segmentation tool on concomitant treatment of characteristic and continuum emission.

    Science.gov (United States)

    Myakalwar, Ashwin Kumar; Dingari, Narahara Chari; Dasari, Ramachandra Rao; Barman, Ishan; Gundawar, Manoj Kumar

    2014-01-01

    We demonstrate the application of non-gated laser induced breakdown spectroscopy (LIBS) for characterization and classification of organic materials with similar chemical composition. While use of such a system introduces substantive continuum background in the spectral dataset, we show that appropriate treatment of the continuum and characteristic emission results in accurate discrimination of pharmaceutical formulations of similar stoichiometry. Specifically, our results suggest that near-perfect classification can be obtained by employing suitable multivariate analysis on the acquired spectra, without prior removal of the continuum background. Indeed, we conjecture that pre-processing in the form of background removal may introduce spurious features in the signal. Our findings in this report significantly advance the prior results in time-integrated LIBS application and suggest the possibility of a portable, non-gated LIBS system as a process analytical tool, given its simple instrumentation needs, real-time capability and lack of sample preparation requirements.

  8. Non-gated laser induced breakdown spectroscopy provides a powerful segmentation tool on concomitant treatment of characteristic and continuum emission.

    Directory of Open Access Journals (Sweden)

    Ashwin Kumar Myakalwar

    Full Text Available We demonstrate the application of non-gated laser induced breakdown spectroscopy (LIBS for characterization and classification of organic materials with similar chemical composition. While use of such a system introduces substantive continuum background in the spectral dataset, we show that appropriate treatment of the continuum and characteristic emission results in accurate discrimination of pharmaceutical formulations of similar stoichiometry. Specifically, our results suggest that near-perfect classification can be obtained by employing suitable multivariate analysis on the acquired spectra, without prior removal of the continuum background. Indeed, we conjecture that pre-processing in the form of background removal may introduce spurious features in the signal. Our findings in this report significantly advance the prior results in time-integrated LIBS application and suggest the possibility of a portable, non-gated LIBS system as a process analytical tool, given its simple instrumentation needs, real-time capability and lack of sample preparation requirements.

  9. A study of internal oxidation in carburized steels by glow discharge optical emission spectroscopy and scanning electron microscopy

    CERN Document Server

    An, X; Rainforth, W M; Chen, L

    2003-01-01

    The internal oxidation of Cr-Mn carburizing steel was studied. Internal oxidation was induced using a commercial carburizing process. Sputter erosion coupled with glow discharge optical emission spectroscopy (GDOES) was used to determine the depth profile elemental distribution within the internal oxidation layer (<10 mu m). In addition, scanning electron microscopy (SEM) equipped with energy dispersive spectrometer (EDS) studies were carried out on selected sputter eroded surfaces. Oxide type was identified primarily by transmission electron microscopy (TEM). The carburized surface was found to consist of a continuous oxide layer, followed by a complex internal oxidation layer, where Cr and Mn oxides were found to populate grain boundaries in a globular form in the near surface region. At greater depths (5-10 mu m), Si oxides formed as a grain boundary network. The internal oxides (mainly complex oxides) grew quickly during the initial stages of the carburizing process (2 h, 800 deg. C+3 h, 930 deg. C). G...

  10. Aqueous solutions of uranium(VI) as studied by time-resolved emission spectroscopy: a round-robin test.

    Science.gov (United States)

    Billard, Isabelle; Ansoborlo, Eric; Apperson, Kathleen; Arpigny, Sylvie; Azenha, M Emilia; Birch, David; Bros, Pascal; Burrows, Hugh D; Choppin, Gregory; Couston, Laurent; Dubois, Veronique; Fanghänel, Thomas; Geipel, Gerhard; Hubert, Solange; Kim, Jae I; Kimura, Takaumi; Klenze, Reinhardt; Kronenberg, Andreas; Kumke, Michael; Lagarde, Gerard; Lamarque, Gerard; Lis, Stefan; Madic, Charles; Meinrath, Gunther; Moulin, Christophe; Nagaishi, Ryuji; Parker, David; Plancque, Gabriel; Scherbaum, Franz; Simoni, Eric; Sinkov, Sergei; Viallesoubranne, Carole

    2003-08-01

    Results of an inter-laboratory round-robin study of the application of time-resolved emission spectroscopy (TRES) to the speciation of uranium(VI) in aqueous media are presented. The round-robin study involved 13 independent laboratories, using various instrumentation and data analysis methods. Samples were prepared based on appropriate speciation diagrams and, in general, were found to be chemically stable for at least six months. Four different types of aqueous uranyl solutions were studied: (1) acidic medium where UO2(2+)aq is the single emitting species, (2) uranyl in the presence of fluoride ions, (3) uranyl in the presence of sulfate ions, and (4) uranyl in aqueous solutions at different pH, promoting the formation of hydrolyzed species. Results between the laboratories are compared in terms of the number of decay components, luminescence lifetimes, and spectral band positions. The successes and limitations of TRES in uranyl analysis and speciation in aqueous solutions are discussed.

  11. Zinc, lead and copper in human teeth measured by induced coupled argon plasma atomic emission spectroscopy (ICP-AES)

    Energy Technology Data Exchange (ETDEWEB)

    Chew, L.T.; Bradley, D.A. E-mail: D.A.Bradley@exeter.ac.uk; Mohd, Y.; Jamil, M

    2000-11-15

    Inductively Coupled Argon Plasma Atomic Emission Spectroscopy (ICP-AES) has been used to determine Pb, Zn and Cu levels in 47 exfoliated human teeth (all of which required extraction for orthodontic reasons). Lead concentrations for the group were 1.7 {mu}g (g tooth mass){sup -1} to 40.5 {mu}g (g tooth mass){sup -1}, with a median of 9.8 {mu}g (g tooth mass){sup -1}. A median lead level in excess of the group value was found for the teeth of six lorry drivers who were included in the study. A more significant enhancement was found for the seven subjects whose age was in excess of 60 years. The median values for Zn and Cu were 123.0 and 0.6 {mu}g (g tooth mass){sup -1} respectively. Present values for tooth-Zn are lower than published data for other ethnic groups.

  12. Comparative measurements of mineral elements in milk powders with laser-induced breakdown spectroscopy and inductively coupled plasma atomic emission spectroscopy.

    Science.gov (United States)

    Lei, W Q; El Haddad, J; Motto-Ros, V; Gilon-Delepine, N; Stankova, A; Ma, Q L; Bai, X S; Zheng, L J; Zeng, H P; Yu, J

    2011-07-01

    Mineral elements contained in commercially available milk powders, including seven infant formulae and one adult milk, were analyzed with inductively coupled plasma atomic emission spectrometry (ICP-AES) and laser-induced breakdown spectroscopy (LIBS). The purpose of this work was, through a direct comparison of the analytical results, to provide an assessment of the performance of LIBS, and especially of the procedure of calibration-free LIBS (CF-LIBS), to deal with organic compounds such as milk powders. In our experiments, the matrix effect was clearly observed affecting the analytical results each time laser ablation was employed for sampling. Such effect was in addition directly observed by determining the physical parameters of the plasmas induced on the different samples. The CF-LIBS procedure was implemented to deduce the concentrations of Mg and K with Ca as the internal reference element. Quantitative analytical results with CF-LIBS were validated with ICP-AES measurements and nominal concentrations specified for commercial milks. The obtained good results with the CF-LIBS procedure demonstrate its capacity to take into account the difference in physical parameters of the plasma in the calculation of the concentrations of mineral elements, which allows a significant reduction of the matrix effect related to laser ablation. We finally discuss the way to optimize the implementation of the CF-LIBS procedure for the analysis of mineral elements in organic materials.

  13. Nondestructive identification of ancient Chinese glasses by Raman and proton-induced X-ray emission spectroscopy

    Institute of Scientific and Technical Information of China (English)

    Hongxia Zhao; Huansheng Cheng; Qinghui Li; Fuxi Gan

    2011-01-01

    @@ Nondestructive Raman spectroscopy and external-beam proton-induced X-ray emission (PIXE) technique to analyze eight ancient glasses unearthed from the provinces of Henan, Hubei, and Jiangsu, which allowes for a good characterization of the glass matrix and chemical compositions, is carried out.The results indicate that all the eight glass samples could be typically divided into three systems: faience (sample No.SZWG-4), PbO-BaO-SiO2 (sample Nos.NYWKI-5-1, HNWKII-88, and HNWKII-84), and Na2O-CaO-SiO2 (sample Nos.HBWKI-16, HBWKI-17, HBWKI-18, and SZWG-1).Additional relationships between the Rarnan spectra and parameters, such as residues of raw materials and opacifying agent, are also discussed by respectively comparing them with similar glass samples excavated from other historical sites.%Nondestructive Raman spectroscopy and external-beam proton-induced X-ray emission (PIXE) technique to analyze eight ancient glasses unearthed from the provinces of Henan, Hubei, and Jiangsu, which allowes for a good characterization of the glass matrix and chemical compositions, is carried out.The results indicate that all the eight glass samples could be typically divided into three systems: faience (sample No.SZWG-4), PbO-BaO-SiO2 (sample Nos.NYWKⅠ-5-1, HNWKⅡ-88, and HNWKⅡ-84), and Na2OCaO-SiO2 (sample Nos.HBWKⅠ-16, HBWKⅠ-17, HBWKⅠ-18, and SZWG-1).Additional relationships between the Raman spectra and parameters, such as residues of raw materials and opacifying agent, are also discussed by respectively comparing them with similar glass samples excavated from other historical sites.

  14. Adsorption, X-ray Diffraction, Photoelectron, and Atomic Emission Spectroscopy Benchmark Studies for the Eighth Industrial Fluid Properties Simulation Challenge*+

    Science.gov (United States)

    Ross, Richard B.; Aeschliman, David B.; Ahmad, Riaz; Brennan, John K.; Brostrom, Myles L.; Frankel, Kevin A.; Moore, Jonathan D.; Moore, Joshua D.; Mountain, Raymond D.; Poirier, Derrick M.; Thommes, Matthias; Shen, Vincent K.; Schultz, Nathan E.; Siderius, Daniel W.; Smith, Kenneth D.

    2016-01-01

    The primary goal of the eighth industrial fluid properties simulation challenge was to test the ability of molecular simulation methods to predict the adsorption of organic adsorbates in activated carbon materials. The challenge focused on the adsorption of perfluorohexane in the activated carbon standard BAM-P109 (Panne and Thünemann 2010). Entrants were challenged to predict the adsorption of perfluorohexane in the activated carbon at a temperature of 273 K and at relative pressures of 0.1, 0.3, and 0.6. The relative pressure (P/Po) is defined as that relative to the bulk saturation pressure predicted by the fluid model at a given temperature (273 K in this case). The predictions were judged by comparison to a set of experimentally determined values, which are published here for the first time and were not disclosed to the entrants prior to the challenge. Benchmark experimental studies, described herein, were also carried out and provided to entrants in order to aid in the development of new force fields and simulation methods to be employed in the challenge. These studies included argon, carbon dioxide, and water adsorption in the BAM-P109 activated carbon as well as X-ray diffraction, X-ray microtomography, photoelectron spectroscopy, and atomic emission spectroscopy studies of BAM-P109. Several concurrent studies were carried out for the BAM-P108 activated carbon (Panne and Thünemann 2010). These are included in the current manuscript for comparison. PMID:27840543

  15. Resonant x-ray emission spectroscopy of liquid water: novel instrumentation, high resolution, and the"map" approach

    Energy Technology Data Exchange (ETDEWEB)

    Weinhardt, L.; Fuchs, O.; Blum, M.; B& #228; r, M.; Weigand, M.; Denlinger, J.D.; Zubavichus, Y.; Zharnikov, M.; Grunze, M.; Heske, C.; Umbach, E.

    2008-06-17

    Techniques to study the electronic structure of liquids are rare. Most recently, resonant x-ray emission spectroscopy (XES) has been shown to be an extremely versatile spectroscopy to study both occupied and unoccupied electronic states for liquids in thermodynamic equilibrium. However, XES requires high-brilliance soft x-ray synchrotron radiation and poses significant technical challenges to maintain a liquid sample in an ultra-high vacuum environment. Our group has therefore developed and constructed a novel experimental setup for the study of liquids, with the long-term goal of investigating the electronic structure of biological systems in aqueous environments. We have developed a flow-through liquid cell in which the liquid is separated from vacuum by a thin Si3N4 or SiC window and which allows a precise control of temperature. This approach has significant advantages compared to static liquids cells used in the past. Furthermore, we have designed a dedicated high-transmission, high-resolution soft x-ray spectrometer. The high transmission makes it possible to measure complete resonant XES"maps" in less than an hour, giving unprecedented detailed insight into the electronic structure of the investigated sample. Using this new equipment we have investigated the electronic structure of liquid water. Furthermore, our XES spectra and maps give information about ultra-fast dissociation on the timescale of the O 1s core hole lifetime, which is strongly affected by the initial state hydrogen bonding configuration.

  16. X-ray emission spectroscopy applied to glycine adsorbed on Cu(110): An atom and symmetry projected view

    Energy Technology Data Exchange (ETDEWEB)

    Hasselstroem, J.; Karis, O.; Weinelt, M. [Uppsala Univ. (Sweden)] [and others

    1997-04-01

    When a molecule is adsorbed on a metal surface by chemical bonding new electronic states are formed. For noble and transition metals these adsorption-induced states overlap with the much more intense metal d-valence band, making them difficult to probe by for instance direct photoemission. However, it has recently been shown that X-ray emission spectroscopy (XES) can be applied to adsorbate systems. Since the intermediate state involves a core hole, this technique has the power to project out the partial density of states around each atomic site. Both the excitation and deexcitation processes are in general governed by the dipole selection rules. For oriented system, it is hence possible to obtain a complete separation into 2p{sub x}, 2p{sub y} and 2p{sub z} contributions using angular resolved measurements. The authors have applied XES together with other core level spectroscopies to glycine adsorption on Cu(110). Glycine (NH{sub 2}CH{sub 2}COOH) is the smallest amino acid and very suitable to study by core level spectroscopy since it has several functional groups, all well separated in energy by chemical shifts. Its properties are futhermore of biological interest. In summary, the authors have shown that it is possible to apply XES to more complicated molecular adsorbates. The assignment of different electronic states is however not as straight forward as for simple diatomic molecules. For a complete understanding of the redistribution and formation of new electronic states associated with the surface chemical bond, experimental data must be compared to theoretical calculations.

  17. Composition variations in Cu{sub 2}ZnSnSe{sub 4} thin films analyzed by X-ray diffraction, energy dispersive X-ray spectroscopy, particle induced X-ray emission, photoluminescence, and Raman spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Nam, Dahyun [Department of Physics, Sogang University, Seoul 121-742 (Korea, Republic of); Opanasyuk, A.S.; Koval, P.V.; Ponomarev, A.G. [Department of Electronics and Computer Technology, Sumy State University, Sumy UA-40007 (Ukraine); Jeong, Ah Reum; Kim, Gee Yeong; Jo, William [Department of Physics, Ewha Womans University, Seoul 120-750 (Korea, Republic of); Cheong, Hyeonsik, E-mail: hcheong@sogang.ac.kr [Department of Physics, Sogang University, Seoul 121-742 (Korea, Republic of)

    2014-07-01

    Compositional and structural studies of Cu{sub 2}ZnSnSe{sub 4} (CZTSe) thin films were carried out by X-ray diffraction, energy dispersive X-ray spectroscopy (EDS), particle induced X-ray emission (PIXE), photoluminescence, and Raman spectroscopy. CZTSe thin films with different compositions were deposited on sodalime glass by co-evaporation. The composition of the films measured by two different methods, EDS and PIXE, showed significant differences. Generally, the Zn/Sn ratio measured by EDS is larger than that measured by PIXE. Both the micro-PIXE and the micro-Raman imaging results indicated the compositional and structural inhomogeneity of the sample. - Highlights: • Particle induced X-ray emission was used to analyze the composition of CZTSe films. • Energy dispersive X-ray spectroscopy tends to underestimate the Sn composition. • Local Raman intensity is related with the composition rather than the crystallinity.

  18. Atmospheric Longwave Infrared Emission Spectroscopy of Water Vapor at the South Pole

    OpenAIRE

    Myers, Brooke A.

    2000-01-01

    The downward infrared radiance spectrum was measured with a Michelson Long Wave Infrared (LWIR) spectrometer at the Amundsen-Scott South Pole Station. Spectra were collected year-round at the South Pole in 1998. This research focuses on the atmospheric water emission lines between 250 and 800 cm-1 (40 to 12.5 μm) region. The spectral resolution is 1 cm-1. The atmosphere over the South Pole is the driest and coldest on Earth. Winter surface temperatures average approximately -60°C, while the t...

  19. Determination of phosphorus in lubricating oils by cool-flame emission spectroscopy.

    Science.gov (United States)

    Elliott, W N; Heathcote, C; Mostyn, R A

    1972-03-01

    The phosphorus content of lubricating oils is determined by measurement of the emission from the HPO molecular species at 528 nm in a cool hydrogen-nitrogen diffusion flame. The oil is ashed in the presence of potassium hydroxide and an aqueous extract of the melt is treated with ion-exchange resin to remove interferents, before aspiration into the flame. Analytical results are presented on samples containing phosphorus in the range 0.009-0.2%. The precision of the method is +/- 5% at the 0.04% phosphorus level.

  20. Evaluation of cross-sections for particle induced gamma-ray emission (PIGE) spectroscopy

    Science.gov (United States)

    Gurbich, A. F.

    2014-07-01

    The extension of the cross-section evaluation procedure to PIGE data was investigated and the first results are reported. Two different cases were studied: the gamma emission accompanying inelastic scattering of protons, and the (p,γ)-reaction. The corresponding theoretical calculations were performed in the framework of R-matrix and DWBA for the (p,p‧γ) reaction on 23Na, and using statistical model for the proton radiative capture by 52Cr. The possibility of achieving a close fit to the experimental data is demonstrated.

  1. Evaluation of cross-sections for particle induced gamma-ray emission (PIGE) spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Gurbich, A.F., E-mail: gurbich@ippe.ru

    2014-07-15

    The extension of the cross-section evaluation procedure to PIGE data was investigated and the first results are reported. Two different cases were studied: the gamma emission accompanying inelastic scattering of protons, and the (p,γ)-reaction. The corresponding theoretical calculations were performed in the framework of R-matrix and DWBA for the (p,p′γ) reaction on {sup 23}Na, and using statistical model for the proton radiative capture by {sup 52}Cr. The possibility of achieving a close fit to the experimental data is demonstrated.

  2. Chemical Analysis of Impurity Boron Atoms in Diamond Using Soft X-ray Emission Spectroscopy

    OpenAIRE

    Muramatsu, Yasuji

    2009-01-01

    To analyze the local structure and/or chemical states of boron atoms in boron-doped diamond, which can be synthesized by the microwave plasma-assisted chemical vapor deposition method (CVD-B-diamond) and the temperature gradient method at high pressure and high temperature (HPT-B-diamond), we measured the soft X-ray emission spectra in the CK and BK regions of B-diamonds using synchrotron radiation at the Advanced Light Source (ALS). X-ray spectral analyses using the fingerprint method and mo...

  3. Comparison Between X-rays Absorption and Emission Spectroscopy Measurements on a Ceramic Envelop Lamp

    Institute of Scientific and Technical Information of China (English)

    Bruno LAFITTE; Michel AUBES; Georges ZISSIS

    2007-01-01

    Burners of metal halide lamps used for illumination are generally made of polycrystalline alumina ceramic (PCA) which is translucent to visible light.We show that the difficulty of selecting a line of sight through the lamp prevents the use of optical emission diagnostic.X-rays photons are mainly absorbed and not scattered by PCA.Absorption by mercury atoms contributing to the discharge allowed us to determine the density of mercury in the lamp.By comparing diagnostic methods,we put in evidence the difficulty of taking into account the scattering of light mathematically.

  4. Study of argon additive in a beam injection type negative ion source using VUV emission spectroscopy

    OpenAIRE

    Nakada, Naoki; Fukumasa, Osamu

    2006-01-01

    Effects of Ar addition are studied by using a beam injection type negative ion source. With adding Ar, I_ increases at low base H_2 pressure. At high base H_2 pressure, however, I_ decreases. VUV emission intensities also decrease at high base pressure. In other words, Ar addition is adverse effect for production of H_2 (v''). Therefore, decrease in I_ is caused by decrease in H_2 (v''). In D_2 plasmas, variation patterns of plasma parameters and VUV intensities by Ar addition are nearly the ...

  5. Further evidence for charge transfer complexes in brown carbon aerosols from excitation-emission matrix fluorescence spectroscopy.

    Science.gov (United States)

    Phillips, Sabrina M; Smith, Geoffrey D

    2015-05-14

    The light-absorbing fraction of organic molecules in ambient aerosols, known as "brown carbon," is an important yet poorly characterized component. Despite the fact that brown carbon could alter the radiative forcing of aerosols significantly, identification of specific chromophores has remained challenging. We recently demonstrated that charge transfer (CT) complexes formed in organic molecules could be responsible for a large fraction of absorption observed in water-extracted ambient particulate matter.1 In the present study, we use excitation-emission matrix fluorescence spectroscopy to further corroborate the importance of CT complexes in defining aerosol optical properties. Monotonically increasing and decreasing quantum yields, decreasing Stokes shifts, and red-shifting emission maxima are observed from ambient particulate matter collected in Athens, Georgia, strongly suggesting that a superposition of independent chromophores is not sufficient to explain brown carbon absorption and fluorescence. Instead, we show that a model in which such chromophores are energetically coupled to a dense manifold of CT complexes is consistent with all of the observations. Further, we suggest that a significant fraction of the observed fluorescence originates from CT complexes and that their contribution to brown carbon absorption is likely greater than we reported previously.

  6. Characterization of direct current He-N{sub 2} mixture plasma using optical emission spectroscopy and mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Flores, O.; Castillo, F.; Martinez, H. [Laboratorio de Espectroscopia, Instituto de Ciencias Físicas, Universidad Nacional Autónoma de México, Apartado Postal 48-3, 62251, Cuernavaca, Morelos (Mexico); Villa, M.; Reyes, P. G. [Facultad de Ciencias, Universidad Autónoma del Estado de México, Estado de México (Mexico); Villalobos, S. [Laboratorio de Espectroscopia, Instituto de Ciencias Físicas, Universidad Nacional Autónoma de México, Apartado Postal 48-3, 62251, Cuernavaca, Morelos (Mexico); Facultad de Ingeniería, Universidad Nacional Autónoma de México, México D.F. (Mexico)

    2014-05-15

    This study analyses the glow discharge of He and N{sub 2} mixture at the pressure of 2.0 Torr, power of 10 W, and flow rate of 16.5 l/min, by using optical emission spectroscopy and mass spectrometry. The emission bands were measured in the wavelength range of 200–1100 nm. The principal species observed were N{sub 2}{sup +} (B{sup 2}Σ{sup +}{sub u}→X{sup 2}Σ{sup +}{sub g}), N{sub 2} (C{sup 3}Π{sub u}→B{sup 3}Π{sub g}), and He, which are in good agreement with the results of mass spectrometry. Besides, the electron temperature and ion density were determined by using a double Langmuir probe. Results indicate that the electron temperature is in the range of 1.55–2.93 eV, and the electron concentration is of the order of 10{sup 10} cm{sup −3}. The experimental results of electron temperature and ion density for pure N{sub 2} and pure He are in good agreement with the values reported in the literature.

  7. Physical Properties of Emission-Line Galaxies at z ~ 2 from Near-Infrared Spectroscopy with Magellan FIRE

    CERN Document Server

    Masters, Daniel; Siana, Brian; Malkan, Matthew; Mobasher, Bahram; Atek, Hakim; Henry, Alaina; Martin, Crystal L; Rafelski, Marc; Hathi, Nimish P; Scarlata, Claudia; Ross, Nathaniel R; Bunker, Andrew J; Blanc, Guillermo A; Bedregal, Alejandro G; Dominguez, Alberto; Colbert, James; Teplitz, Harry; Dressler, Alan

    2014-01-01

    We present results from near-infrared spectroscopy of 26 emission-line galaxies at z ~ 2 obtained with the FIRE spectrometer on the Magellan Baade telescope. The sample was selected from the WISP survey, which uses the near-infrared grism of the Hubble Space Telescope Wide Field Camera 3 to detect emission-line galaxies over 0.3 1 star-forming galaxies, but composite spectra derived from the sample do not show an appreciable offset from the local star-forming sequence on the [O III]/H-beta versus [S II]/H-alpha diagram. We infer a high nitrogen-to-oxygen abundance ratio from the composite spectrum, which may contribute to the offset of the high-redshift galaxies from the local star-forming sequence in the [O III]/H-beta versus [N II]/H-alpha diagram. We speculate that the elevated nitrogen abundance could result from substantial numbers of Wolf-Rayet stars in starbursting galaxies at z~2. (Abridged)

  8. The Nature of Extreme Emission Line Galaxies at z=1-2: Kinematics and Metallicities from Near-Infrared Spectroscopy

    CERN Document Server

    Maseda, Michael V; Rix, Hans-Walter; da Cunha, Elisabete; Pacifici, Camilla; Momcheva, Ivelina; Brammer, Gabriel B; Meidt, Sharon E; Franx, Marijn; van Dokkum, Pieter; Fumagalli, Mattia; Bell, Eric F; Ferguson, Henry C; Förster-Schreiber, Natascha M; Koekemoer, Anton M; Koo, David C; Lundgren, Britt F; Marchesini, Danilo; Nelson, Erica J; Patel, Shannon G; Skelton, Rosalind E; Straughn, Amber N; Trump, Jonathan R; Whitaker, Katherine E

    2014-01-01

    We present near-infrared spectroscopy of a sample of 22 Extreme Emission Line Galaxies at redshifts 1.3 5) and [N II]/H{\\alpha} is always significantly below unity, which suggests a low gas-phase metallicity. We are able to determine gas-phase metallicities for 7 of our objects using various strong-line methods, with values in the range 0.05-0.30 Z_sun and with a median of 0.15 Z_sun; for 3 of these objects we detect [O III]{\\lambda}4363 which allows for a direct constraint on the metallicity. The velocity dispersion, as measured from the nebular emission lines, is typically ~50 km/s. Combined with the observed star-forming activity, the Jeans and Toomre stability criteria imply that the gas fraction must be large (> 2/3), consistent with the difference between our dynamical and stellar mass estimates. The implied gas depletion time scale (several hundred Myr) is substantially longer than the inferred mass-weighted ages (~50 Myr), which further supports the emerging picture that most stars in low-mass galaxi...

  9. Fast Detection Allows Analysis of the Electronic Structure of Metalloprotein by X-ray Emission Spectroscopy at Room Temperature.

    Science.gov (United States)

    Davis, Katherine M; Mattern, Brian A; Pacold, Joseph I; Zakharova, Taisiya; Brewe, Dale; Kosheleva, Irina; Henning, Robert W; Graber, Timothy J; Heald, Steve M; Seidler, Gerald T; Pushkar, Yulia

    2012-07-19

    The paradigm of "detection-before-destruction" was tested for a metalloprotein complex exposed at room temperature to the high x-ray flux typical of third generation synchrotron sources. Following the progression of the x-ray induced damage by Mn Kβ x-ray emission spectroscopy, we demonstrated the feasibility of collecting room temperature data on the electronic structure of native Photosystem II, a trans-membrane metalloprotein complex containing a Mn(4)Ca cluster. The determined non-damaging observation timeframe (about 100 milliseconds using continuous monochromatic beam, deposited dose 1*10(7) photons/µm(2) or 1.3*10(4) Gy, and 66 microseconds in pulsed mode using pink beam, deposited dose 4*10(7) photons/µm(2) or 4.2*10(4) Gy) is sufficient for the analysis of this protein's electron dynamics and catalytic mechanism at room temperature. Reported time frames are expected to be representative for other metalloproteins. The described instrumentation, based on the short working distance dispersive spectrometer, and experimental methodology is broadly applicable to time-resolved x-ray emission analysis at synchrotron and x-ray free-electron laser light sources.

  10. Extended wavelength anisotropy resolved multidimensional emission spectroscopy (ARMES) measurements: better filters, validation standards, and Rayleigh scatter removal methods

    Science.gov (United States)

    Casamayou-Boucau, Yannick; Ryder, Alan G.

    2017-09-01

    Anisotropy resolved multidimensional emission spectroscopy (ARMES) provides valuable insights into multi-fluorophore proteins (Groza et al 2015 Anal. Chim. Acta 886 133-42). Fluorescence anisotropy adds to the multidimensional fluorescence dataset information about the physical size of the fluorophores and/or the rigidity of the surrounding micro-environment. The first ARMES studies used standard thin film polarizers (TFP) that had negligible transmission between 250 and 290 nm, preventing accurate measurement of intrinsic protein fluorescence from tyrosine and tryptophan. Replacing TFP with pairs of broadband wire grid polarizers enabled standard fluorescence spectrometers to accurately measure anisotropies between 250 and 300 nm, which was validated with solutions of perylene in the UV and Erythrosin B and Phloxine B in the visible. In all cases, anisotropies were accurate to better than ±1% when compared to literature measurements made with Glan Thompson or TFP polarizers. Better dual wire grid polarizer UV transmittance and the use of excitation-emission matrix measurements for ARMES required complete Rayleigh scatter elimination. This was achieved by chemometric modelling rather than classical interpolation, which enabled the acquisition of pure anisotropy patterns over wider spectral ranges. In combination, these three improvements permit the accurate implementation of ARMES for studying intrinsic protein fluorescence.

  11. A synthetic diagnostic for beam emission spectroscopy in the helically symmetric experiment stellarator

    Science.gov (United States)

    Dobbins, T. J.; Kumar, S. T. A.; Anderson, D. T.

    2016-11-01

    The Helically Symmetric Experiment (HSX) has a number of active spectroscopy diagnostics. Due to the relatively large beam width compared to the plasma minor radius, it is difficult to achieve good spatial resolution at the core of the HSX plasma. This is due to the fact that the optical sightline cuts through many flux surfaces with varying field vectors within the beam. In order to compare the experimental results with theoretical models it is important to accurately model the beam width effects. A synthetic diagnostic has been developed for this purpose. This synthetic diagnostic calculates the effect of spot size and beam width on the measurements of quantities of interest, including radial electric field, flow velocity, and Stark polarization.

  12. Glow discharge optical emission spectroscopy for accurate and well resolved analysis of coatings and thin films

    KAUST Repository

    Wilke, Marcus

    2011-12-01

    In the last years, glow discharge optical emission spectrometry (GDOES) gained more and more acceptance in the analysis of functional coatings. GDOES thereby represents an interesting alternative to common depth profiling techniques like AES and SIMS, based on its unique combination of high erosion rates and erosion depths, sensitivity, analysis of nonconductive layers and easy quantification even for light elements such as C, N, O and H. Starting with the fundamentals of GDOES, a short overview on new developments in instrument design for accurate and well resolved thin film analyses is presented. The article focuses on the analytical capabilities of glow discharge optical emission spectrometry in the analysis of metallic coatings and thin films. Results illustrating the high depth resolution, confirmation of stoichiometry, the detection of light elements in coatings as well as contamination on the surface or interfaces will be demonstrated by measurements of: a multilayer system Cr/Ti on silicon, interface contamination on silicon during deposition of aluminum, Al2O3-nanoparticle containing conversion coatings on zinc for corrosion resistance, Ti3SiC2 MAX-phase coatings by pulsed laser deposition and hydrogen detection in a V/Fe multilayer system. The selected examples illustrate that GDOES can be successfully adopted as an analytical tool in the development of new materials and coatings. A discussion of the results as well as of the limitations of GDOES is presented. © 2011 Elsevier B.V.

  13. Suzaku Spectroscopy Study of Hard X-Ray Emission in the Arches Cluster

    CERN Document Server

    Tsujimoto, M; Koyama, K

    2006-01-01

    We present the results of a Suzaku study of the Arches cluster. A high S/N spectrum in the 3-12 keV band was obtained with the XIS. We found that the spectrum consists of a thermal plasma, a hard power-law tail, and two Gaussian lines. The plasma component (kT~2.2 keV) is established from the presence of CaXIX and FeXXV K alpha lines as well as the absence of FeXXVI K alpha line. The two Gaussian lines represent the K alpha and beta lines from iron at lower ionization stages. Both the line centers and the intensity ratio of these two lines are consistent with the neutral iron. The hard power-law tail (index~0.7) was found to have no pronounced iron K edge feature. In comparison with the published Chandra spectra, we conclude that the thermal component is from the ensemble of point-like sources plus thermal diffuse emission concentrated at the cluster center, while the Gaussian and the hard tail components are from the non-thermal diffuse emission extended in a larger scale. In the band-limited XIS images, the...

  14. IFU Spectroscopy of 10 ETG nuclei: Properties of the circumnuclear gas emission

    Science.gov (United States)

    Ricci, T. V.

    2015-09-01

    LINERs are galactic nuclei containing spectra with prominence of low-ionization lines. Several ionization sources are able to produce a LINER-like spectra (e.g. shocks, low-luminosity AGNs, pAGB stars). In this work, we will present an analysis performed on a sample of 10 massive ETGs with distances up to 30 Mpc. This sample was observed with the GMOS-IFU installed on the Gemini-South Telescope. The data cubes of the galaxies have a FOV of 3.5 - 5 arcsec2 and a spatial resolution of about 0.6 -- 1.0 arcsec. After subtracting the stellar component of the galaxies by means of spectral synthesis, we studied the emission lines all over the FOV of the data cubes. In galaxies where an AGN was clearly detected, we found ionized gaseous discs and also a low-velocity extended emission perpendicular to the gas discs. We concluded that only ionizing photons emerging from the AGNs are not enough to photoionize the gaseous discs of the galaxies. On the other hand, it seems to be responsible for the photoionization of the low-velocity extended gas perpendicular to the discs. We propose a scheme where some collimating agent, somehow aligned to the gaseous discs, may be present in some LINER-like AGNs in the local universe.

  15. Field emission spectroscopy evidence for dual-barrier electron tunnelling in nanographite

    Energy Technology Data Exchange (ETDEWEB)

    Bandurin, D. A.; Kleshch, V. I. [Department of Physics, M.V. Lomonosov Moscow State University, Moscow 119991 (Russian Federation); Mingels, S.; Lützenkirchen-Hecht, D.; Müller, G. [FB C Physics Department, University of Wuppertal, 42119 Wuppertal (Germany); Obraztsov, A. N., E-mail: obraz@polly.phys.msu.ru [Department of Physics, M.V. Lomonosov Moscow State University, Moscow 119991 (Russian Federation); Department of Physics and Mathematics, University of Eastern Finland, Joensuu 80101 (Finland)

    2015-06-08

    Nanocarbon films with upstanding flake-like graphite crystallites of nanometre thickness were fabricated by carbon condensation from a methane–hydrogen gas mixture activated by a direct-current discharge. The nanographite (NG) crystallites are composed of a few graphene layers. The adjacent atomic layers are connected partially at the edges of the crystallites to form strongly curved graphene structures. The extraordinary field emission (FE) properties were revealed for the NG films with an average current density of a few mA/cm{sup 2}, reproducibly obtained at a macroscopic applied field of about 1 V/μm. The integral FE current–voltage curves and electron spectra (FEES) of NG cathodes with multiple emitters were measured in a triode configuration. Most remarkably, above a threshold field, two peaks were revealed in FEES with different field-dependent shifts to lower energies. This behaviour evidences electron emission through a dual potential barrier, corresponding to carbon–carbon heterostructure formed as a result of the graphene bending.

  16. Spectroscopy of southern Galactic disk planetary nebulae. Notes on chemical composition and emission-line stars

    CERN Document Server

    Górny, S K

    2014-01-01

    We present low resolution spectroscopic observations for a sample of 53 planetary nebulae (PNe) located in the southern sky between Vela and Norma constellations and pertaining to the Galactic disk with expected Galactocentric distance range of 5 to 10 kpc. We derive nebular chemical composition and plasma parameters with the classical empirical method. For most of the observed objects it is done for the first time. The distributions of the chemical abundances of the observed disk sample are generally indistinguishable from Galactic bulge and inner-disk PNe populations. The exceptions are possible differences in He/H distribution comparing to bulge PNe and Ne/Ar comparing to inner-disk PNe sample. The derived O/H ratios for the observed disk PNe fit to the concept of flattening of the chemical gradient in the inner parts of the Milky Way. We use the spectra to search for emission-line central stars in the observed sample. We found 6 new emission-line central stars comprising examples of all known types: WEL, ...

  17. Investigation of local thermodynamic equilibrium of laser induced Al2O3-TiC plasma in argon by spatially resolved optical emission spectroscopy

    Science.gov (United States)

    Alnama, K.; Alkhawwam, A.; Jazmati, A. K.

    2016-06-01

    Plasma plume of Al2O3-TiC is generated by third harmonic Q-switched Nd:YAG nanosecond laser. It is characterized using Optical Emission Spectroscopy (OES) at different argon background gas pressures 10, 102, 103, 104 and 105 Pa. Spatial evolution of excitation and ionic temperatures is deduced from spectral data analysis. Temporal evolution of Ti I emission originated from different energy states is probed. The correlation between the temporal behavior and the spatial temperature evolution are investigated under LTE condition for the possibility to use the temporal profile of Ti I emission as an indicator for LTE validity in the plasma.

  18. Investigation of local thermodynamic equilibrium of laser induced Al2O3–TiC plasma in argon by spatially resolved optical emission spectroscopy

    Directory of Open Access Journals (Sweden)

    K. Alnama

    2016-06-01

    Full Text Available Plasma plume of Al2O3–TiC is generated by third harmonic Q-switched Nd:YAG nanosecond laser. It is characterized using Optical Emission Spectroscopy (OES at different argon background gas pressures 10, 102, 103, 104 and 105 Pa. Spatial evolution of excitation and ionic temperatures is deduced from spectral data analysis. Temporal evolution of Ti I emission originated from different energy states is probed. The correlation between the temporal behavior and the spatial temperature evolution are investigated under LTE condition for the possibility to use the temporal profile of Ti I emission as an indicator for LTE validity in the plasma.

  19. Resonant X-ray emission spectroscopy reveals d-d ligand-field states involved in the self-assembly of a square-planar platinum complex.

    Science.gov (United States)

    Garino, Claudio; Gallo, Erik; Smolentsev, Nikolay; Glatzel, Pieter; Gobetto, Roberto; Lamberti, Carlo; Sadler, Peter J; Salassa, Luca

    2012-11-28

    Resonant X-ray Emission Spectroscopy (RXES) is used to characterize the ligand field states of the prototypic self-assembled square-planar complex, [Pt(tpy)Cl]Cl (tpy=2,2':6',2''-terpyridine), and determine the effect of weak metal-metal and π-π interactions on their energy.

  20. Relativistic plasma optics enabled by near-critical density nanostructured material

    CERN Document Server

    Bin, J H; Wang, H Y; Streeter, M J V; Kreuzer, C; Kiefer, D; Yeung, M; Cousens, S; Foster, P S; Dromey, B; Yan, X Q; Meyer-ter-Vehn, J; Zepf, M; Schreiber, J

    2014-01-01

    The nonlinear optical properties of a plasma due to the relativistic electron motion in an intense laser field are of fundamental importance for current research and the generation of brilliant laser-driven sources of particles and photons1-15. Yet, one of the most interesting regimes, where the frequency of the laser becomes resonant with the plasma, has remained experimentally hard to access. We overcome this limitation by utilizing ultrathin carbon nanotube foam16 (CNF) targets allowing the strong relativistic nonlinearities at near- critical density (NCD) to be exploited for the first time. We report on the experimental realization of relativistic plasma optics to spatio-temporally compress the laser pulse within a few micrometers of propagation, while maintaining about half its energy. We also apply the enhanced laser pulses to substantially improve the properties of an ion bunch accelerated from a secondary target. Our results provide first insights into the rich physics of NCD plasmas and the opportuni...

  1. Exoplanet atmosphere. Thermal structure of an exoplanet atmosphere from phase-resolved emission spectroscopy.

    Science.gov (United States)

    Stevenson, Kevin B; Désert, Jean-Michel; Line, Michael R; Bean, Jacob L; Fortney, Jonathan J; Showman, Adam P; Kataria, Tiffany; Kreidberg, Laura; McCullough, Peter R; Henry, Gregory W; Charbonneau, David; Burrows, Adam; Seager, Sara; Madhusudhan, Nikku; Williamson, Michael H; Homeier, Derek

    2014-11-14

    Exoplanets that orbit close to their host stars are much more highly irradiated than their solar system counterparts. Understanding the thermal structures and appearances of these planets requires investigating how their atmospheres respond to such extreme stellar forcing. We present spectroscopic thermal emission measurements as a function of orbital phase ("phase-curve observations") for the highly irradiated exoplanet WASP-43b spanning three full planet rotations using the Hubble Space Telescope. With these data, we construct a map of the planet's atmospheric thermal structure, from which we find large day-night temperature variations at all measured altitudes and a monotonically decreasing temperature with pressure at all longitudes. We also derive a Bond albedo of 0.18(-0.12)(+0.07) and an altitude dependence in the hot-spot offset relative to the substellar point.

  2. Thermal structure of an exoplanet atmosphere from phase-resolved emission spectroscopy

    CERN Document Server

    Stevenson, Kevin B; Line, Michael R; Bean, Jacob L; Fortney, Jonathan J; Showman, Adam P; Kataria, Tiffany; Kreidberg, Laura; McCullough, Peter R; Henry, Gregory W; Charbonneau, David; Burrows, Adam; Seager, Sara; Madhusudhan, Nikku; Williamson, Michael H; Homeier, Derek

    2014-01-01

    Exoplanets that orbit close to their host stars are much more highly irradiated than their Solar System counterparts. Understanding the thermal structures and appearances of these planets requires investigating how their atmospheres respond to such extreme stellar forcing. We present spectroscopic thermal emission measurements as a function of orbital phase ("phase-curve observations") for the highly-irradiated exoplanet WASP-43b spanning three full planet rotations using the Hubble Space Telescope. With these data, we construct a map of the planet's atmospheric thermal structure, from which we find large day-night temperature variations at all measured altitudes and a monotonically decreasing temperature with pressure at all longitudes. We also derive a Bond albedo of 0.18 +0.07,-0.12 and an altitude dependence in the hot-spot offset relative to the substellar point.

  3. Determination of the electron energy distribution function of a low temperature plasma from optical emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Dodt, Dirk Hilar

    2009-01-05

    The experimental determination of the electron energy distribution of a low pressure glow discharge in neon from emission spectroscopic data has been demonstrated. The spectral data were obtained with a simple overview spectrometer and analyzed using a strict probabilistic, Bayesian data analysis. It is this Integrated Data Analysis (IDA) approach, which allows the significant extraction of non-thermal properties of the electron energy distribution function (EEDF). The results bear potential as a non-invasive alternative to probe measurements. This allows the investigation of spatially inhomogeneous plasmas (gradient length smaller than typical probe sheath dimensions) and plasmas with reactive constituents. The diagnostic of reactive plasmas is an important practical application, needed e.g. for the monitoring and control of process plasmas. Moreover, the experimental validation of probe theories for magnetized plasmas as a long-standing topic in plasma diagnostics could be addressed by the spectroscopic method. (orig.)

  4. Development of a Reference Database for Particle-Induced Gamma-ray Emission spectroscopy

    Science.gov (United States)

    Dimitriou, P.; Becker, H.-W.; Bogdanović-Radović, I.; Chiari, M.; Goncharov, A.; Jesus, A. P.; Kakuee, O.; Kiss, A. Z.; Lagoyannis, A.; Räisänen, J.; Strivay, D.; Zucchiatti, A.

    2016-03-01

    Particle-Induced Gamma-ray Emission (PIGE) is a powerful analytical technique that exploits the interactions of rapid charged particles with nuclei located near a sample surface to determine the composition and structure of the surface regions of solids by measurement of characteristic prompt γ rays. The potential for depth profiling of this technique has long been recognized, however, the implementation has been limited owing to insufficient knowledge of the physical data and lack of suitable user-friendly computer codes for the applications. Although a considerable body of published data exists in the nuclear physics literature for nuclear reaction cross sections with γ rays in the exit channel, there is no up-to-date, comprehensive compilation specifically dedicated to IBA applications. A number of PIGE cross-section data had already been uploaded to the Ion Beam Analysis Nuclear Data Library (IBANDL)

  5. Determination of ammonium and organic bound nitrogen by inductively coupled plasma emission spectroscopy.

    Science.gov (United States)

    Jaber, A M Y; Mehanna, N A; Sultan, S M

    2009-06-15

    The continuous flow sample introduction technique with a hydride generator system in conjunction with an inductively coupled plasma emission spectrometer (ICP-AES-HG), is used in this study for quantitative determination of ammonium and organic bound nitrogen in aqueous and solid samples. Ammonia vapor released from ammonium salt after treatment with concentrated NaOH is transferred by argon to plasma for detection at 174.273 nm using axial argon plasma mode. The calibration curves were linear within a range of 25-1000 mg L(-1)N as ammonium molybdate with correlation coefficients of better than 0.99 and limits of detection of about 10-25mg L(-1)N. The percent recovery of N (25-500 mg L(-1)N) in soft (distilled) water and high salt content (1.7 mol L(-1) NaCl) matrices was found to be in the range of about 97-102% with %RSD in the range of 4.6-0.62. The sensitivity, limit of detection, and blank contribution from the atmospheric nitrogen, were tremendously improved in this method compared with the available ICP-AES spray chamber counterpart. Furthermore, the ICP-AES-HG method gave results for real samples (soil, fertilizer, waste water) containing about 50-1800 mg L(-1)N in good agreement with those obtained by the standard Kjeldahl method. No statistical differences at the 95% confidence level on applying the t-test were observed between the values obtained by the two methods. Thus, the ICP-AES-HG method is reliable and faster than the conventional tedious Kjeldahl method, superior to the ICP-AES spray chamber method, and almost free from matrix interference which is usually a critical factor in atomic emission spectroscopic techniques.

  6. Single and double core-hole ion emission spectroscopy of transient neon plasmas produced by ultraintense x-ray laser pulses

    Science.gov (United States)

    Gao, Cheng; Zeng, Jiaolong; Yuan, Jianmin

    2016-05-01

    Single core-hole (SCH) and double core-hole (DCH) spectroscopy is investigated systematically for neon gas in the interaction with ultraintense x-ray pulses with photon energy from 937 eV to 2000 eV. A time-dependent rate equation, implemented in the detailed level accounting approximation, is utilized to study the dynamical evolution of the level population and emission properties of the laser-produced highly transient plasmas. The plasma density effects on level populations are demonstrated with an x-ray photon energy of 2000 eV. For laser photon energy in the range of 937 - 1360 eV, resonant absorptions (RA) of 1s-np (n> = 2) transitions play important roles in time evolution of the population and DCH emission spectroscopy. For x-ray photon energy larger than 1360 eV, no RA exist and transient plasmas show different features in the DCH spectroscopy.

  7. Measuring reactive nitrogen emissions from point sources using visible spectroscopy from aircraft.

    Science.gov (United States)

    Melamed, M L; Solomon, S; Daniel, J S; Langford, A O; Portmann, R W; Ryerson, T B; Nicks, D K; McKeen, S A

    2003-02-01

    Accurate measurements of nitrogen dioxide (NO2), a key trace gas in the formation and destruction of tropospheric ozone, are important in studies of urban pollution. Nitrogen dioxide column abundances were measured during the Texas Air Quality Study 2000 using visible absorption spectroscopy from an aircraft. The method allows for quantification of the integrated total number of nitrogen dioxide molecules in the polluted atmosphere and is hence a useful tool for measuring plumes of this key trace gas. Further, we show how such remote-sensing observations can be used to obtain information on the fluxes of nitrogen dioxide into the atmosphere with unique flexibility in terms of aircraft altitude, and the height and extent of mixing of the boundary layer. Observations of nitrogen dioxide plumes downwind of power plants were used to estimate the flux of nitrogen oxide emitted from several power plants in the Houston and Dallas metropolitan areas and in North Carolina. Measurements taken over the city of Houston were also employed to infer the total flux from the city as a whole.

  8. Source fingerprint monitoring of air pollutants from petrochemical industry and the determination of their annual emission flux using open path Fourier transform infrared spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Yih-Shiaw Huang; Shih-Yi Chang; Tai-Ly Tso [National Tsing Hua Univ., Hsinchu (China)

    1996-12-31

    Toxic air pollutants were investigated in several petrochemical industrial park in Taiwan using a movable open-path Fourier-transform infrared spectroscopy (FTIR). The results show the qualitative and quantitative analysis of emission gases from plants, and also provide the emission rates of various compounds. More than twenty compounds under usual operation were found from these industrial park. The concentration variation with time could be correlated exactly with the distances from the emission source along the wind direction. This means that by changing the measuring points the source of emission could be unambiguously identified. The point, area and line source (PAL) plume dispersion model has been applied to estimate the emission rate of either a point or an area source. The local atmospheric stability was determined by releasing an SF{sub 6} tracer. The origin of errors came mainly from the uncertainty of the source configuration and the variation of the meteorological condition. Through continuous measurement using a portable open-path Fourier transform infrared (POP-FTIR) spectrometer, the maximum value of the emission rate and the annual amount of emission could be derived. The emission rate of the measured toxic gases was derived by the model technique, and the results show that the emission amount is on the order of ten to hundred tons per year.

  9. Development of wavelength-dispersive soft X-ray emission spectrometers for transmission electron microscopes--an introduction of valence electron spectroscopy for transmission electron microscopy.

    Science.gov (United States)

    Terauchi, Masami; Koike, Masato; Fukushima, Kurio; Kimura, Atsushi

    2010-01-01

    Two types of wavelength-dispersive soft X-ray spectrometers, a high-dispersion type and a conventional one, for transmission electron microscopes were constructed. Those spectrometers were used to study the electronic states of valence electrons (bonding electrons). Both spectrometers extended the acceptable energy regions to higher than 2000 eV. The best energy resolution of 0.08 eV was obtained for an Al L-emission spectrum by using the high-dispersion type spectrometer. By using the spectrometer, C K-emission of carbon allotropes, Cu L-emission of Cu(1-x)Zn(x) alloys and Pt M-emission spectra were presented. The FWHM value of 12 eV was obtained for the Pt Malpha-emission peak. The performance of the conventional one was also presented for ZnS and a section specimen of a multilayer device. W-M and Si-K emissions were clearly resolved. Soft X-ray emission spectroscopy based on transmission electron microscopy (TEM) has an advantage for obtaining spectra from a single crystalline specimen with a defined crystal setting. As an example of anisotropic soft X-ray emission, C K-emission spectra of single crystalline graphite with different crystal settings were presented. From the spectra, density of states of pi- and sigma-bondings were separately derived. These results demonstrated a method to analyse the electronic states of valence electrons of materials in the nanometre scale based on TEM.

  10. Measuring PAH Emission in Ultradeep Spitzer IRS Spectroscopy of High Redshift IR Luminous Galaxies

    CERN Document Server

    Teplitz, H I; Armus, L; Chary, R; Marshall, J A; Colbert, J W; Frayer, D T; Pope, A; Blain, A; Spoon, H; Charmandaris, V; Scott, D

    2007-01-01

    The study of the dominant population of high redshift IR-luminous galaxies (10^11 - 10^12 Lsun at 1emission in all four targets, and compare the spectra to those of local galaxies observed by the IRS. The z=1.09 source appears to be a typical, star-formation dominated IR-luminous galaxy, while the z=2.69 source is a composite source with strong star formation and a prominent AGN. The IRAC colors of this source show no evidence of rest-frame near-infrared stellar photospheric...

  11. Emission spectroscopy of an atmospheric pressure plasma jet operated with air at low frequency

    Science.gov (United States)

    Giuliani, L.; Gallego, J. L.; Minotti, F.; Kelly, H.; Grondona, D.

    2015-03-01

    Low-temperature, high-pressure plasma jets have an extensive use in plasma biology and plasma medicine, such as pathogen deactivation, wound disinfection, stopping of bleeding without damage of healthy tissue, acceleration of wound healing, control of bio-film proliferation, etc. In this work, a spectroscopic characterization of a typical plasma jet, operated in air at atmospheric pressure, is reported. Within the spectrum of wavelengths from 200 to 450 nm all remarkable emissions of N2 were monitored. Spectra of the N2 2nd positive system (C3Πu-B3Πg) emitted in air are the most convenient for plasma diagnostics, since they enable to determine electronic Te, rotational Tr and vibrational Tv temperatures by fitting the experimental spectra with the simulated ones. We used SPECAIR software for spectral simulation and obtained the best fit with all these temperatures about 3500K. The conclusion that all temperatures are equal, and its relatively high value, is consistent with the results of a previous work, where it was found that the experimentally determined electrical characteristic was consistent with the model of a thermal arc discharge, together with a highly collisional cathode sheet.

  12. Changes in dissolved organic matter quality in a northern hardwood forest revealed by excitation emission spectroscopy

    Science.gov (United States)

    Saraceno, J.; Shanley, J. B.; Pellerin, B. A.; Hansen, A. M.

    2016-12-01

    Changes in dissolved organic matter (DOM) quality may result from unusual and extreme precipitation patterns such as floods and droughts. In order to study DOM quality changes, we collected several hundred surface water samples during the past eight years from the W-9 watershed of the Sleepers River Research Watershed in Danville, Vermont for optical analysis of dissolved organic matter. We present the results of parallel factor (PARAFAC) and principal component analysis (PCA) on excitation emission matrices (EEMs). This analysis revealed that peaks T, C and M as identified by PARAFAC were the most prominent EEM features. The intensity of these peaks varied on inter-annual, seasonal and event time periods and these shifts reflect changes in DOM quality. Likely drivers of this variability in DOM chemistry are seasonal shifts in flow paths, antecedent moisture conditions, and precipitation duration and intensity. For example, during events, the relative proportion of protein-like, peak T fluorophores increased, likely from flushing of fresh polyphenols from surficial and shallow flow paths. During the winter, when groundwater dominates flow, EEMs were strong in humic-like peak C and peak M fluorophores, reflecting deeper soil sources and longer flow paths. Our analyses will reveal how DOM quality responds to climatic drivers, and thus how we can expect DOM quality to evolve under projected climate change scenarios.

  13. Vibrational Motions Associated with Primary Processes in Bacteriorhodopsin Studied by Coherent Infrared Emission Spectroscopy

    Science.gov (United States)

    Groma, Géza I.; Colonna, Anne; Martin, Jean-Louis; Vos, Marten H.

    2011-01-01

    The primary energetic processes driving the functional proton pump of bacteriorhodopsin take place in the form of complex molecular dynamic events after excitation of the retinal chromophore into the Franck-Condon state. These early events include a strong electronic polarization, skeletal stretching, and all-trans-to-13-cis isomerization upon formation of the J intermediate. The effectiveness of the photoreaction is ensured by a conical intersection between the electronic excited and ground states, providing highly nonadiabatic coupling to nuclear motions. Here, we study real-time vibrational coherences associated with these motions by analyzing light-induced infrared emission from oriented purple membranes in the 750–1400 cm−1 region. The experimental technique applied is based on second-order femtosecond difference frequency generation on macroscopically ordered samples that also yield information on phase and direction of the underlying motions. Concerted use of several analysis methods resulted in the isolation and characterization of seven different vibrational modes, assigned as C-C stretches, out-of-plane methyl rocks, and hydrogen out-of-plane wags, whereas no in-plane H rock was found. Based on their lifetimes and several other criteria, we deduce that the majority of the observed modes take place on the potential energy surface of the excited electronic state. In particular, the direction sensitivity provides experimental evidence for large intermediate distortions of the retinal plane during the excited-state isomerization process. PMID:21402041

  14. Optimal emission enhancement in orthogonal double-pulse laser-induced breakdown spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Sanginés, R. [Centro de Ciencias Aplicadas y Desarrollo Tecnológico, Universidad Nacional Autónoma de México (CCADET-UNAM), Apartado Postal 70-186, México, DF 04510 (Mexico); Cátedra CONACyT, Centro de Nanociencias y Nanotecnología, Universidad Nacional Autónoma de México, Apartado Postal 14, Ensenada, BC 22800 (Mexico); Contreras, V. [Department of Physics, Tampere University of Technology, P.O. Box 692, FI-33101 Tampere (Finland); Sobral, H., E-mail: martin.sobral@ccadet.unam.mx [Centro de Ciencias Aplicadas y Desarrollo Tecnológico, Universidad Nacional Autónoma de México (CCADET-UNAM), Apartado Postal 70-186, México, DF 04510 (Mexico); Robledo-Martinez, A. [Universidad Autónoma Metropolitana-Unidad Azcapotzalco, Av. San Pablo 180, Azcapotzalco, México, DF 02200 (Mexico)

    2015-08-01

    Orthogonal double-pulse (DP) laser-induced breakdown spectroscopy (LIBS) was performed using reheating and pre-ablative configurations. The ablation pulse power density was varied by two orders of magnitude and the DP experiments were carried out for a wide range of interpulse delays. For both DP-LIBS schemes, the signal enhancement was evaluated with respect to the corresponding single-pulse (SP) LIBS as a function of the interpulse delay. The reheating scheme shows a sharp maximum signal enhancement of up to 200-fold for low ablative power densities (0.4 GW cm{sup −2}); however, for power densities larger than 10 GW cm{sup −2} this configuration did not improve the SP outcome. On the other hand, a more uniform signal enhancement of about 4–6 was obtained for the pre-ablative scheme nearly independently of the used ablative power density. In terms of the signal-to-noise ratio (SNR) the pre-ablative scheme shows a monotonic increment with the ablative power density. Whereas the reheating configuration reaches a maximum at 2.2 GW cm{sup −2}, its enhancement effect collapses markedly for fluencies above 10 GW cm{sup −2}. - Highlights: • Comparison of reheating and pre-ablative double-pulse LIBS was done using a wide range of ablation power densities. • Experimental parameters that could achieve optimal signal-to-noise ratio were investigated. • A reheating scheme is better for low-ablation power densities. • A pre-ablative configuration is better for high-ablation power densities.

  15. X-ray Emission Spectroscopy to Study Ligand Valence Orbitals in Mn Coordination Complexes

    Energy Technology Data Exchange (ETDEWEB)

    Smolentsev, Grigory; Soldatov, Alexander V; Messinger, Johannes; Merz, Kathrin; Weyhermuller, Thomas; Bergmann, Uwe; Pushkar, Yulia; Yano, Junko; Yachandra, Vittal K.; Glatzel, Pieter

    2009-03-02

    We discuss a spectroscopic method to determine the character of chemical bonding and for the identification of metal ligands in coordination and bioinorganic chemistry. It is based on the analysis of satellite lines in X-ray emission spectra that arise from transitions between valence orbitals and the metal ion 1s level (valence-to-core XES). The spectra, in connection with calculations based on density functional theory (DFT), provide information that is complementary to other spectroscopic techniques, in particular X-ray absorption (XANES and EXAFS). The spectral shape is sensitive to protonation of ligands and allows ligands, which differ only slightly in atomic number (e.g., C, N, O...), to be distinguished. A theoretical discussion of the main spectral features is presented in terms of molecular orbitals for a series of Mn model systems: [Mn(H2O)6]2+, [Mn(H2O)5OH]+, [Mn(H2O)5NH2]+, and [Mn(H2O)5NH3]2+. An application of the method, with comparison between theory and experiment, is presented for the solvated Mn2+ ion in water and three Mn coordination complexes, namely [LMn(acac)N3]BPh4, [LMn(B2O3Ph2)(ClO4)], and [LMn(acac)N]BPh4, where L represents 1,4,7-trimethyl-1,4,7-triazacyclononane, acac stands for the 2,4-pentanedionate anion, and B2O3Ph2 represents the 1,3-diphenyl-1,3-dibora-2-oxapropane-1,3-diolato dianion.

  16. Energy level spectroscopy of InSb quantum wells using quantum-well LED emission

    Science.gov (United States)

    Tenev, T. G.; Palyi, A.; Mirza, B. I.; Nash, G. R.; Fearn, M.; Smith, S. J.; Buckle, L.; Emeny, M. T.; Ashley, T.; Jefferson, J. H.; Lambert, C. J.

    2009-02-01

    We have investigated the low-temperature optical properties of InSb quantum-well (QW) light-emitting diodes, with different barrier compositions, as a function of well width. Three devices were studied: QW1 had a 20 nm undoped InSb quantum well with a barrier composition of Al0.143In0.857Sb , QW2 had a 40 nm undoped InSb well with a barrier composition of Al0.077In0.923Sb , and QW3 had a 100 nm undoped InSb well with a barrier composition of Al0.025In0.975Sb . For QW1, the signature of two transitions (CB1-HH1 and CB1-HH2) can be seen in the measured spectrum, whereas for QW2 and QW3 the signature of a large number of transitions is present in the measured spectra. In particular transitions to HH2 can be seen, the first time this has been observed in AlInSb/InSb heterostructures. To identify the transitions that contribute to the measured spectra, the spectra have been simulated using an eight-band k.p calculation of the band structure together with a first-order time-dependent perturbation method (Fermi golden rule) calculation of spectral emittance, taking into account broadening. In general there is good agreement between the measured and simulated spectra. For QW2 we attribute the main peak in the experimental spectrum to the CB2-HH1 transition, which has the highest overall contribution to the emission spectrum of QW2 compared with all the other interband transitions. This transition normally falls into the category of “forbidden transitions,” and in order to understand this behavior we have investigated the momentum matrix elements, which determine the selection rules of the problem.

  17. Dynamics of bolaamphiphilic fluorescent polyenes in lipid bilayers from polarization emission spectroscopy.

    Science.gov (United States)

    Acuña, A Ulises; Amat-Guerri, Francisco; Quesada, Ernesto; Vélez, Marisela

    2006-06-20

    The rotational motions of the biamphiphilic polyenes (bolapolyenes) dimethyl all-(E)-octacosa-10,12,14,16,18-pentaenedioate (DE28:5) and dimethyl all-(E)-tetratriaconta-13,15,17,19,21-pentaenedioate (DE34:5), with head-to-head distances of 34 and 42A, respectively, have been examined by fluorescence anisotropy methods. The membrane-spanning bolapolyenes, which contain a central emitting pentaene group tethered to two methoxycarbonyl opposite polar heads by symmetric C(8) (DE28:5) and C(11) (DE34:5) polymethylene chains, were dispersed in lipid bilayers of DPPC or DMPC, and the stationary and picosecond-resolved emission was recorded as a function of temperature. In fluid-phase DMPC bilayers, three relaxation times could be determined, assigned to fast (0.2 and 2ns) single-bond isomerization processes localized on the alkyl chains, and to whole-molecule oscillations ( approximately 11ns), respectively. The anisotropy decay parameters were further analyzed in terms of a diffusive model for wobbling in a Gaussian ordering potential, to assess the anchoring effect of the symmetric polar heads. In this way, the average rotational diffusion constant of the bolapolyenes, D( perpendicular), could be estimated as 0.022-0.026rad(2) ns(-1) (DMPC bilayers, 35 degrees Celsius), a value that is only 1/3 of that corresponding to the related pentaene fatty acid spanning a single membrane monolayer. In contrast, the amplitude of the equilibrium orientational distribution (theta(half-cone) approximately 50 degrees ) is very similar for both the transmembrane and the single-headed polyenes. The reorientational oscillations of the central emitting group in the bolapolyenes necessarily would produce large-amplitude (2-5A) and very fast (ns) translational motions of the polar heads.

  18. FLASH SPECTROSCOPY: EMISSION LINES FROM THE IONIZED CIRCUMSTELLAR MATERIAL AROUND <10-DAY-OLD TYPE II SUPERNOVAE

    Energy Technology Data Exchange (ETDEWEB)

    Khazov, D.; Yaron, O.; Gal-Yam, A.; Manulis, I.; Rubin, A.; Ofek, E. O.; Horesh, A. [Benoziyo Center for Astrophysics, Faculty of Physics, The Weizmann Institute for Science, Rehovot 76100 (Israel); Kulkarni, S. R.; Kasliwal, M. M.; Cao, Y.; Perley, D. [Astronomy Department, California Institute of Technology, 1200 E. California Boulevard, Pasadena, CA 91125 (United States); Arcavi, I.; Howell, D. A. [Las Cumbres Observatory Global Telescope Network, 6740 Cortona Drive, Suite 102, Goleta, CA 93111 (United States); Sollerman, J. [The Oskar Klein Centre, Department of Astronomy, Stockholm University, AlbaNova, SE-10691 Stockholm (Sweden); Sullivan, M. [School of Physics and Astronomy, University of Southampton, Southampton, SO17 1BJ (United Kingdom); Filippenko, A. V.; Nugent, P. E. [Department of Astronomy, University of California, Berkeley, CA 94720-3411 (United States); Cenko, S. B. [Astrophysics Science Division, NASA Goddard Space Flight Center, Mail Code 661, Greenbelt, MD 20771 (United States); Silverman, J. M. [Department of Astronomy, University of Texas at Austin, Austin, TX 78712 (United States); Ebeling, H. [Institute for Astronomy, University of Hawaii, 2680 Woodlawn Drive, Honolulu, HI 96822 (United States); and others

    2016-02-10

    Supernovae (SNe) embedded in dense circumstellar material (CSM) may show prominent emission lines in their early-time spectra (≤10 days after the explosion), owing to recombination of the CSM ionized by the shock-breakout flash. From such spectra (“flash spectroscopy”), we can measure various physical properties of the CSM, as well as the mass-loss rate of the progenitor during the year prior to its explosion. Searching through the Palomar Transient Factory (PTF and iPTF) SN spectroscopy databases from 2009 through 2014, we found 12 SNe II showing flash-ionized (FI) signatures in their first spectra. All are younger than 10 days. These events constitute 14% of all 84 SNe in our sample having a spectrum within 10 days from explosion, and 18% of SNe II observed at ages <5 days, thereby setting lower limits on the fraction of FI events. We classified as “blue/featureless” (BF) those events having a first spectrum that is similar to that of a blackbody, without any emission or absorption signatures. It is possible that some BF events had FI signatures at an earlier phase than observed, or that they lack dense CSM around the progenitor. Within 2 days after explosion, 8 out of 11 SNe in our sample are either BF events or show FI signatures. Interestingly, we found that 19 out of 21 SNe brighter than an absolute magnitude M{sub R} = −18.2 belong to the FI or BF groups, and that all FI events peaked above M{sub R} = −17.6 mag, significantly brighter than average SNe II.

  19. Resonant soft X-ray emission spectroscopy of vanadium oxides andrelated compounds

    Energy Technology Data Exchange (ETDEWEB)

    Schmitt, Thorsten

    2004-11-01

    In today's information world, bits of data are processed by semiconductor chips, and stored in the magnetic disk drives. But tomorrow's information technology may see magnetism (spin) and semiconductivity (charge) combined in one ''spintronic'' device that exploits both charge and ''spin'' to carry data (the best of two worlds). Spintronic devices such as spin valve transistors, spin light emitting diodes, non-volatile memory, logic devices, optical isolators and ultra-fast optical switches are some of the areas of interest for introducing the ferromagnetic properties at room temperature in a semiconductor to make it multifunctional. The potential advantages of such spintronic devices will be higher speed, greater efficiency, and better stability at a reduced power consumption. This Thesis contains two main topics: In-depth understanding of magnetism in Mn doped ZnO, and our search and identification of at least six new above room temperature ferromagnetic semiconductors. Both complex doped ZnO based new materials, as well as a number of nonoxides like phosphides, and sulfides suitably doped with Mn or Cu are shown to give rise to ferromagnetism above room temperature. Some of the highlights of this work are discovery of room temperature ferromagnetism in: (1) ZnO:Mn (paper in Nature Materials, Oct issue, 2003); (2) ZnO doped with Cu (containing no magnetic elements in it); (3) GaP doped with Cu (again containing no magnetic elements in it); (4) Enhancement of Magnetization by Cu co-doping in ZnO:Mn; and (5) CdS doped with Mn, and a few others not reported in this thesis. We discuss in detail the first observation of ferromagnetism above room temperature in the form of powder, bulk pellets, in 2-3 {micro}m thick transparent pulsed laser deposited films of the Mn (< 4 at.%) doped ZnO. High-resolution transmission electron microscopy (HRTEM) and electron energy loss spectroscopy (EELS) spectra recorded from 2 to 200nm

  20. Resonant soft X-ray emission spectroscopy of vanadium oxides andrelated compounds

    Energy Technology Data Exchange (ETDEWEB)

    Schmitt, Thorsten [Uppsala Univ. (Sweden)

    2004-01-01

    In today's information world, bits of data are processed by semiconductor chips, and stored in the magnetic disk drives. But tomorrow's information technology may see magnetism (spin) and semiconductivity (charge) combined in one ''spintronic'' device that exploits both charge and ''spin'' to carry data (the best of two worlds). Spintronic devices such as spin valve transistors, spin light emitting diodes, non-volatile memory, logic devices, optical isolators and ultra-fast optical switches are some of the areas of interest for introducing the ferromagnetic properties at room temperature in a semiconductor to make it multifunctional. The potential advantages of such spintronic devices will be higher speed, greater efficiency, and better stability at a reduced power consumption. This Thesis contains two main topics: In-depth understanding of magnetism in Mn doped ZnO, and our search and identification of at least six new above room temperature ferromagnetic semiconductors. Both complex doped ZnO based new materials, as well as a number of nonoxides like phosphides, and sulfides suitably doped with Mn or Cu are shown to give rise to ferromagnetism above room temperature. Some of the highlights of this work are discovery of room temperature ferromagnetism in: (1) ZnO:Mn (paper in Nature Materials, Oct issue, 2003); (2) ZnO doped with Cu (containing no magnetic elements in it); (3) GaP doped with Cu (again containing no magnetic elements in it); (4) Enhancement of Magnetization by Cu co-doping in ZnO:Mn; and (5) CdS doped with Mn, and a few others not reported in this thesis. We discuss in detail the first observation of ferromagnetism above room temperature in the form of powder, bulk pellets, in 2-3 μm thick transparent pulsed laser deposited films of the Mn (< 4 at.%) doped ZnO. High-resolution transmission electron microscopy (HRTEM) and electron energy loss spectroscopy (EELS) spectra recorded from 2 to 200nm

  1. Magnetic Resonance Spectroscopy and Single-Photon Emission Computed Tomography in the Evaluation of Cerebral Tumors: A Case Report

    Science.gov (United States)

    Siasios, Ioannis; Valotassiou, Varvara; Kapsalaki, Eftychia; Tsougos, Ioannis; Georgoulias, Panagiotis; Fotiadou, Aggeliki; Ioannou, Maria; Koukoulis, Georgios; Dimopoulos, Vassilios; Fountas, Kostas

    2017-01-01

    In their daily clinical practice, physicians have to confront diagnostic dilemmas which cannot be resolved by the application of only one imaging technique. In this case report, we present a 66-year-old woman who was admitted to our institution for the surgical resection of a recently diagnosed brain tumor. The patient had a history of epileptic seizures and was hospitalized in the past for anti-phospholipid syndrome related to a non-Hodgkin lymphoma in remission. Magnetic resonance imaging (MRI) examination revealed an enhancing right parasagittal lesion with significant edema suggestive of a high grade glioma. Advanced MRI techniques including proton magnetic resonance spectroscopy (1H-MRS) showed findings compatible of glioma. An additional examination was performed as part of a protocol that we are routinely performing in our institution for all brain tumors including not only the gold standard advanced MRI techniques but also single-photon emission computed tomography (SPECT) with technetium-99m (Tc99m). Brain SPECT indicated the presence of a meningioma which was verified by the histopathology of the resected specimen. In conclusion, a multimodality approach for the pre-surgical assessment of brain tumors has significant advantages not only for the diagnosis but also for the evaluation of intracranial tumors histology. PMID:27924180

  2. Fingerprinting of complex mixtures with the use of high performance liquid chromatography, inductively coupled plasma atomic emission spectroscopy and chemometrics

    Energy Technology Data Exchange (ETDEWEB)

    Ni Yongnian [Department of Chemistry, Nanchang University, Nanchang, Jiangxi 330047 (China)], E-mail: ynni@ncu.edu.cn; Peng Yunyan [Department of Chemistry, Nanchang University, Nanchang, Jiangxi 330047 (China); Kokot, Serge [Inorganic Materials Program, School of Physical and Chemical Sciences, Queensland University of Technology, Brisbane, Queensland 4001 (Australia)

    2008-05-26

    The molecular and metal profile fingerprints were obtained from a complex substance, Atractylis chinensis DC-a traditional Chinese medicine (TCM), with the use of the high performance liquid chromatography (HPLC) and inductively coupled plasma atomic emission spectroscopy (ICP-AES) techniques. This substance was used in this work as an example of a complex biological material, which has found application as a TCM. Such TCM samples are traditionally processed by the Bran, Cut, Fried and Swill methods, and were collected from five provinces in China. The data matrices obtained from the two types of analysis produced two principal component biplots, which showed that the HPLC fingerprint data were discriminated on the basis of the methods for processing the raw TCM, while the metal analysis grouped according to the geographical origin. When the two data matrices were combined into a one two-way matrix, the resulting biplot showed a clear separation on the basis of the HPLC fingerprints. Importantly, within each different grouping the objects separated according to their geographical origin, and they ranked approximately in the same order in each group. This result suggested that by using such an approach, it is possible to derive improved characterisation of the complex TCM materials on the basis of the two kinds of analytical data. In addition, two supervised pattern recognition methods, K-nearest neighbors (KNNs) method, and linear discriminant analysis (LDA), were successfully applied to the individual data matrices-thus, supporting the PCA approach.

  3. Optical emission spectroscopy of deuterium and helium plasma jets emitted from plasma focus discharges at the PF-1000U facility

    Science.gov (United States)

    Skladnik-Sadowska, E.; Dan'ko, S. A.; Kwiatkowski, R.; Sadowski, M. J.; Zaloga, D. R.; Paduch, M.; Zielinska, E.; Kharrasov, A. M.; Krauz, V. I.

    2016-12-01

    Optical emission spectroscopy techniques were used to investigate the spectra of dense deuterium-plasma jets generated by high-current pulse discharges within the large PF-1000U facility and to estimate parameters of plasma inside the jets and their surroundings. Time-resolved optical spectra were recorded by means of a Mechelle®900 spectrometer. From an analysis of the deuterium line broadening, it was estimated that the electron concentration at a distance 57 cm from the electrode outlets amounted to (0.4-3.7) × 1017 cm-3 depending on the initial gas distribution and the time interval of the spectrum registration after the instant of the plasma jet generation. From the re-absorption dip in the Dβ profile, it was assessed that the electron concentration in the surrounding gas was equal to about 1.5 × 1015 cm-3. On the basis of the measured ratio of He II 468.6 nm and He I 587.6 nm line intensities, it was estimated that the electron temperature amounted to about 5.3 eV. Also estimated were some dimensionless parameters of the investigated plasma jets.

  4. Elemental Content in Brown Rice by Inductively Coupled Plasma Atomic Emission Spectroscopy Reveals the Evolution of Asian Cultivated Rice

    Institute of Scientific and Technical Information of China (English)

    Yawen Zeng; Luxiang Wang; Juan Du; Jiafu Liu; Shuming Yang; Xiaoying Pu; Fenghui Xiao

    2009-01-01

    The phylogenetic relationship for classification traits and eight mineral elements in brown rice (Oryza sativa L.) from Yunnan Province in China was carried out using microwave assisted digestion followed by inductively coupled plasma atomic emission spectroscopy, and the analytical procedures were carefully controlled and validated. In general, the results show that the mean levels of K, Ca, Mg, Fe and Cu in brown rice for 789 accessions of rice landraces was distinctly lower than that of improved cultivars. They further demonstrate that Ca plays an important role in the differentiation of subspecies indica-japonica, especially to enhance adaptation of cold stress, and that five mineral elements in brown rice enhance the eurytopicity from landrace to improved cultivar. Hierarchical cluster analysis, using average linkage from SPSS software based on eight mineral elements in brown rice, showed that Yunnan rice could be grouped into rice landrace and improved cultivar, with the rice landrace being further clustered into five subgroups, and that, interestingly, purple rice does not cluster with either of the groups. Our present data confirm that indica is the closest relative of late rice and white rice, and that they constitute rice landraces together, whereas japonica is the closest relatives of non-nuda, early-mid and glutinous rice. It is further shown that japonica, non-nuda, early-mid, glutinous, white and red rice might be more primitive than indica, nuda, late, non-glutinous and purple rice, respectively.

  5. 57Fe emission Mössbauer spectroscopy following dilute implantation of 57Mn into In 2O3

    Science.gov (United States)

    Mokhles Gerami, A.; Johnston, K.; Gunnlaugsson, H. P.; Nomura, K.; Mantovan, R.; Masenda, H.; Matveyev, Y. A.; Mølholt, T. E.; Ncube, M.; Shayestehaminzadeh, S.; Unzueta, I.; Gislason, H. P.; Krastev, P. B.; Langouche, G.; Naidoo, D.; Ólafsson, S.

    2016-12-01

    Emission Mössbauer spectroscopy has been utilised to characterize dilute 57Fe impurities in In 2O3 following implantation of 57Mn ( T 1/2 = 1.5 min.) at the ISOLDE facility at CERN. From stoichiometry considerations, one would expect Fe to adopt the valence state 3 + , substituting In 3+, however the spectra are dominated by spectral lines due to paramagnetic Fe2+. Using first principle calculations in the framework of density functional theory (DFT), the density of states of dilute Fe and the hyperfine parameters have been determined. The hybridization between the 3d-band of Fe and the 2p band of oxygen induces a spin-polarized hole on the O site close to the Fe site, which is found to be the cause of the Fe2+ state in In 2O3. Comparison of experimental data to calculated hyperfine parameters suggests that Fe predominantly enters the 8b site rather than the 24d site of the cation site in the Bixbyite structure of In 2O3. A gradual transition from an amorphous to a crystalline state is observed with increasing implantation/annealing temperature.

  6. Research as a guide for curriculum development: An example from introductory spectroscopy. II. Addressing student difficulties with atomic emission spectra

    Science.gov (United States)

    Ivanjek, L.; Shaffer, P. S.; McDermott, L. C.; Planinic, M.; Veza, D.

    2015-02-01

    This is the second of two closely related articles (Paper I and Paper II) that together illustrate how research in physics education has helped guide the design of instruction that has proved effective in improving student understanding of atomic spectroscopy. Most of the more than 1000 students who participated in this four-year investigation were science majors enrolled in the introductory calculus-based physics course at the University of Washington (UW) in Seattle, WA, USA. The others included graduate and undergraduate teaching assistants at UW and physics majors in introductory and advanced physics courses at the University of Zagreb, Zagreb, Croatia. About half of the latter group were preservice high school physics teachers. Paper I describes how several conceptual and reasoning difficulties were identified among university students as they tried to relate a discrete line spectrum to the energy levels of atoms in a light source. This second article (Paper II) illustrates how findings from this research informed the development of a tutorial that led to improvement in student understanding of atomic emission spectra.

  7. Characterization of low temperature graphene synthesis in inductively coupled plasma chemical vapor deposition process with optical emission spectroscopy.

    Science.gov (United States)

    Ma, Yifei; Kim, Daekyoung; Jang, Haegyu; Cho, Sung Min; Chae, Heeyeop

    2014-12-01

    Low-temperature graphene was synthesized at 400 degrees C with inductively coupled plasma chemical vapor deposition (PECVD) process. The effects of plasma power and flow rate of various carbon containing precursors and hydrogen on graphene properties were investigated with optical emission spectroscopy (OES). Various radicals monitored by OES were correlated with graphene film properties such as sheet resistance, I(D)/I(G) ratio of Raman spectra and transparency. C2H2 was used as a main precursor and the increase of plasma power enhanced intensity of carbon (C2) radical OES intensity in plasma, reduced sheet resistance and increased transparency of graphene films. The reduced flow rate of C2H2 decreased sheet resistance and increased transparency of graphene films in the range of this study. H2 addition was found to increase sheet resistance, transparency and attributed to reduction of graphene grain and etching graphene layers. OES analysis showed that C2 radicals contribute to graphite networking and sheet resistance reduction. TEM and AFM were applied to provide credible information that graphene had been successfully grown at low temperature.

  8. Spectroscopy of superluminous supernova host galaxies. A preference of hydrogen-poor events for extreme emission line galaxies

    CERN Document Server

    Leloudas, G; Kruehler, T; Gorosabel, J; Christensen, L; Mehner, A; Postigo, A de Ugarte; Amorin, R; Thoene, C C; Anderson, J P; Bauer, F E; Gallazzi, A; Helminiak, K G; Hjorth, J; Ibar, E; Malesani, D; Morell, N; Vinko, J; Wheeler, J C

    2014-01-01

    Superluminous supernovae (SLSNe) were only discovered recently due to their preference for occurring in faint dwarf galaxies. Understanding why stellar evolution yields different types of stellar explosions in these environments is fundamental in order to both uncover the elusive progenitors of SLSNe and to study star formation in dwarf galaxies. In this paper, we present the first results of our project to study SUperluminous Supernova Host galaxIES (SUSHIES), focusing on the sample for which we have obtained spectroscopy. We show that SLSNe-I and SLSNe-R (hydrogen-poor) often (~50% in our sample) occur in a class of galaxies that is known as Extreme Emission Line Galaxies (EELGs). The probability of this happening by chance is negligible and we therefore conclude that the extreme environmental conditions and the SLSN phenomenon are related. In contrast, SLSNe-II (hydrogen-rich) occur in more massive, more metal-rich galaxies with softer radiation fields. Therefore, if SLSNe-II constitute a uniform class, th...

  9. Determination of plasma trace elements in tumor-bearing animals by proton-induced X-ray emission spectroscopy.

    Science.gov (United States)

    Fogle, M; Daly, B; Evans, M; Justiniano, E L; Kovacs, C J; Shinpaugh, J L; Toburen, L H

    2001-11-01

    Although altered levels of circulating essential trace elements are known to accompany malignant disease, the lack of sensitivity of conventional detection methods has generally limited their study to clinical conditions involving extensive disease (i.e., significant tumor burden). As such, the application of altered trace element levels as potential prognostic guides or as response indicators subsequent to treatment has been of limited use. During this study, proton-induced X-ray emission spectroscopy was evaluated as a tool to determine trace element imbalances in a murine tumor model. Using plasma from C57B1/6 mice bearing the syngeneic Lewis lung carcinoma (LLCa), levels of Fe, Cu, and Zn, as well as changes in the Cu /Zn ratio, were measured in animals carrying an increasing primary tumor burden. The plasma levels of Fe, Cu, and Zn were found to decrease significantly 7 d following implants of LLCa cells with no significant change observed in the Cu/Zn ratio. By d 21, however, an increase in the Cu/Zn ratio was found to accompany increased growth of the LLCa tumor; the plasma levels of Cu had returned to normal levels, whereas both the Fe and Zn plasma levels remained lowered. Collectively, the results suggest that although a net change in individual plasma trace element concentrations might not be accurately associated with tumor growth, a clear relationship was established between the Cu/Zn ratio and tumor size.

  10. Optical emission spectroscopy of OH lines in N2 and Ar plasma during the treatments of cotton fabric

    Science.gov (United States)

    Skoro, Nikola; Puac, Nevena; Spasic, Kosta; Malovic, Gordana; Gorjanc, Marija; Petrovic, Zoran Lj

    2016-09-01

    Low pressure non-equilibrium plasmas are proven to be irreplaceable tool in material processing. Among other fields their applications in treatments of textiles are still diversifying, but the main role of plasma is activation of the surface of treated sample. After, or during, the treatments these surfaces can be covered with different materials or species (such as microcapsules) that enhance properties of the fabric. In order to investigate mechanisms how active species from plasma interact with the cotton surface, we studied both plasma and surface properties. Bleached cotton samples were treated in low-pressure nitrogen and argon plasma in a chamber with parallel-plate electrodes. The effect of the plasma treatment on the cotton samples was investigated with the colorimetric measurements on dyes absorption by a spectrophotometer. Optical emission spectroscopy was performed by using spectrometer with a sensitive CCD camera. We have recorded the evolution of the maximum of the intensity of OH and N2 second positive band lines. Measurement were done with and without samples in the chamber and comparison between the lines intensity was made. The parameters for optimal plasma treatment conditions were determined. Research supported by the MESTD, projects III41011 and ON171037.

  11. A combined FTIR and infrared emission spectroscopy investigation of layered double hydroxide as an effective electron donor

    Science.gov (United States)

    Zhang, Jia; Wei, Feng; Liang, Ying; Zhou, Jizhi; Xi, Yunfei; Qian, Guangren; Frost, Ray

    2016-02-01

    A novel method has been presented to characterize electron transfer in layered double hydroxides (LDHs) utilizing an investigation combing FTIR and infrared emission spectroscopy. At room temperature, electron could transfer to interlayer Fe3 + through monodentate ligand cyanide, and resulted in a reduction of 40% Fe3 + to Fe2 +. When the environmental temperature increased from 25 to 300 °C, reduction of Fe3 + and Ni2 + increased to 94% and 42%. Furthermore, electron also transferred to interlayer cation through multidentate ligand EDTA. As a result, LDHs has been proven to be an effective electron donor, and FTIR was a feasible tool in characterizing this property by monitoring the valence state of cations. It was also concluded that octahedral units with OH- groups in LDH layer functioned as electron donor centers. Driving force for electron transfer is attributed to the charge density difference between cation layer and probe anion. These results could help to explain the mechanism of various applications of LDHs in catalysis and photocatalysis.

  12. Research as a guide for curriculum development: An example from introductory spectroscopy. I. Identifying student difficulties with atomic emission spectra

    Science.gov (United States)

    Ivanjek, L.; Shaffer, P. S.; McDermott, L. C.; Planinic, M.; Veza, D.

    2015-01-01

    This is the first of two closely related articles (Paper I and Paper II) that together illustrate how research in physics education has helped guide the design of instruction that has proved effective in improving student understanding of atomic spectroscopy. Most of the more than 1000 students who participated in this four-year investigation were science majors enrolled in the introductory calculus-based physics course at the University of Washington (UW) in Seattle, WA, USA. The others included graduate and undergraduate teaching assistants at UW and physics majors in introductory and advanced physics courses at the University of Zagreb, Zagreb, Croatia. About half of the latter group were preservice high school physics teachers. This article (Paper I) describes how several serious conceptual and reasoning difficulties were identified among students as they tried to relate a discrete line spectrum to the energy levels of atoms in a light source. Paper II illustrates how findings from this research informed the development of a tutorial that led to significant improvement in student understanding of atomic emission spectra.

  13. Diagnosis of Methane Plasma Generated in an Atmospheric Pressure DBD Micro-Jet by Optical Emission Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    ZHANG Jun-Feng; BIAN Xin-Chao; CHEN Qiang; LIU Fu-Ping; LIU Zhong-Wei

    2009-01-01

    Diagnosis of methane plasma,generated in an atmospheric pressure dielectric barrier discharge (DBD) microplasma jet with a quartz tube as dielectric material by a 25 kHz sinusoidal ac power source,is conducted by optical emission spectroscopy (OES).The reactive radicals in methane plasma such as CH,C2,and Ha are detected insitu by OES.The possible dissociation mechanism of methane in diluted Ar plasma is deduced from spectra.In addition,the density of CH radical,which is considered as one of the precursors in diamond-like (DLC) film formation,affected by the parameters of input voltage and the feed gas flow rate,is emphasized. With the Boltzmann plots,four Ar atomic spectral lines (located at 675.28nm,687.13nm,738.40nm and 794.82nm,respectively) are chosen to calculate the electron temperature,and the dependence of electron temperature on discharge parameters is also investigated.

  14. Insufficiency of Positron Emission Tomography and Magnetic Resonance Spectroscopy in the Diagnosis of Intravascular Lymphoma of the Central Nervous System

    Directory of Open Access Journals (Sweden)

    Nobuyuki Kawai

    2012-07-01

    Full Text Available Intravascular large B-cell lymphoma (IVL is a rare type of extranodal lymphoma with an aggressive clinical course characterized by the proliferation of lymphoma cells within the lumen of small vessels. Diagnosis is often difficult because of marked variability in clinical presentation and nonspecific laboratory and radiological findings, especially when central nervous system (CNS symptoms are the only manifestation. Modern metabolic imaging techniques such as positron emission tomography (PET and 1H-magnetic resonance spectroscopy (MRS have been reported to be useful in the diagnosis of conventional primary CNS lymphoma. We report the case of a 69-year-old man who presented with a progressive leukoencephalopathic syndrome. The patient was examined by 18F-fluorodeoxyglucose and 11C-methionine PET and MRS, but none of these examinations were able to show the presence of a tumor in the lesions or to clarify the tumor characteristics. Brain biopsy was the only way to obtain a definite diagnosis of IVL. The patient was treated intensively with standard immunochemotherapy but died 6 months after the diagnosis. Here, we discuss the insufficiency of modern metabolic imaging techniques, including PET and MRS, and recommend a rapid decision of brain biopsy in the diagnosis of IVL only involving the CNS.

  15. Standard test method for determining elements in waste Streams by inductively coupled plasma-atomic emission spectroscopy

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 This test method covers the determination of trace, minor, and major elements in waste streams by inductively coupled plasma-atomic emission spectroscopy (ICP-AES) following an acid digestion of the sample. Waste streams from manufacturing processes of nuclear and non-nuclear materials can be analyzed. This test method is applicable to the determination of total metals. Results from this test method can be used to characterize waste received by treatment facilities and to formulate appropriate treatment recipes. The results are also usable in process control within waste treatment facilities. 1.2 This test method is applicable only to waste streams that contain radioactivity levels that do not require special personnel or environmental protection. 1.3 A list of the elements determined in waste streams and the corresponding lower reporting limit is found in Table 1. 1.4 This test method has been used successfully for treatment of a large variety of waste solutions and industrial process liquids. The com...

  16. Physical properties of emission-line galaxies at z ∼ 2 from near-infrared spectroscopy with Magellan fire

    Energy Technology Data Exchange (ETDEWEB)

    Masters, Daniel; Siana, Brian; Mobasher, Bahram; Domínguez, Alberto [Department of Physics and Astronomy, University of California, Riverside, CA 92521 (United States); McCarthy, Patrick; Blanc, Guillermo; Dressler, Alan [Carnegie Observatories, Pasadena, CA 91101 (United States); Malkan, Mathew; Ross, Nathaniel R. [Department of Physics and Astronomy, UCLA, Los Angeles, CA 90095 (United States); Atek, Hakim [Laboratoire d' Astrophysique Ecole Polytechnique Fédérale, CH-1290 Sauverny (Switzerland); Henry, Alaina [Astrophysics Science Division, Goddard Space Flight Center, Greenbelt, MD 20771 (United States); Martin, Crystal L. [Department of Physics, Universitey of California, Santa Barbara, CA 93106 (United States); Rafelski, Marc; Colbert, James [Spitzer Science Center, California Institute of Technology, Pasadena, CA 91125 (United States); Hathi, Nimish P. [Aix Marseille Université, CNRS, LAM (Laboratoire d' Astrophysique de Marseille) UMR 7326, F-13388 Marseille (France); Scarlata, Claudia [Minnesota Institute for Astrophysics, University of Minnesota, Minneapolis, MN 55455 (United States); Bunker, Andrew J. [Department of Physics, University of Oxford (United Kingdom); Bedregal, Alejandro G. [Department of Physics and Astronomy, Tufts University, Medford, MA 02155 (United States); Teplitz, Harry [Infrared Processing and Analysis Center, Caltech, Pasadena, CA 91125 (United States)

    2014-04-20

    We present results from near-infrared spectroscopy of 26 emission-line galaxies at z ∼ 2.2 and z ∼ 1.5 obtained with the Folded-port InfraRed Echellette (FIRE) spectrometer on the 6.5 m Magellan Baade telescope. The sample was selected from the WFC3 Infrared Spectroscopic Parallels survey, which uses the near-infrared grism of the Hubble Space Telescope Wide Field Camera 3 (WFC3) to detect emission-line galaxies over 0.3 ≲ z ≲ 2.3. Our FIRE follow-up spectroscopy (R ∼ 5000) over 1.0-2.5 μm permits detailed measurements of the physical properties of the z ∼ 2 emission-line galaxies. Dust-corrected star formation rates for the sample range from ∼5-100 M {sub ☉} yr{sup –1} with a mean of 29 M {sub ☉} yr{sup –1}. We derive a median metallicity for the sample of 12 + log(O/H) = 8.34 or ∼0.45 Z {sub ☉}. The estimated stellar masses range from ∼10{sup 8.5}-10{sup 9.5} M {sub ☉}, and a clear positive correlation between metallicity and stellar mass is observed. The average ionization parameter measured for the sample, log U ≈ –2.5, is significantly higher than what is found for most star-forming galaxies in the local universe, but similar to the values found for other star-forming galaxies at high redshift. We derive composite spectra from the FIRE sample, from which we measure typical nebular electron densities of ∼100-400 cm{sup –3}. Based on the location of the galaxies and composite spectra on diagnostic diagrams, we do not find evidence for significant active galactic nucleus activity in the sample. Most of the galaxies, as well as the composites, are offset diagram toward higher [O III]/Hβ at a given [N II]/Hα, in agreement with other observations of z ≳ 1 star-forming galaxies, but composite spectra derived from the sample do not show an appreciable offset from the local star-forming sequence on the [O III]/Hβ versus [S II]/Hα diagram. We infer a high nitrogen-to-oxygen abundance ratio from the composite spectrum, which

  17. THE SMARTS MULTI-EPOCH OPTICAL SPECTROSCOPY ATLAS (SaMOSA): AN ANALYSIS OF EMISSION LINE VARIABILITY IN SOUTHERN HEMISPHERE FERMI BLAZARS

    Energy Technology Data Exchange (ETDEWEB)

    Isler, Jedidah C. [Chancellor’s Faculty Fellow, Syracuse University, Department of Physics, Syracuse, NY 13244 (United States); Urry, C. M.; Bailyn, C.; Coppi, P.; Brady, M.; MacPherson, E.; Hasan, I.; Buxton, M. [Department of Astronomy, Yale University, P.O. Box 208101, New Haven, CT 06520-8101 (United States); Smith, P. S., E-mail: jcisler@syr.edu [Steward Observatory, University of Arizona, 933 N. Cherry Avenue, Tuscon, AZ 85721 (United States)

    2015-05-01

    We present multi-epoch optical spectroscopy of seven southern Fermi-monitored blazars from 2008 to 2013 using the Small and Medium Aperture Research Telescope System (SMARTS), with supplemental spectroscopy and polarization data from the Steward Observatory. We find that the emission lines are much less variable than the continuum; four of seven blazars had no detectable emission line variability over the 5 yr observation period. This is consistent with photoionization primarily by an accretion disk, allowing us to use the lines as a probe of disk activity. Comparing optical emission line flux with Fermi γ-ray flux and optical polarized flux, we investigate whether relativistic jet variability is related to the accretion flow. In general, we see no such dependence, suggesting that the jet variability is likely caused by internal processes like turbulence or shock acceleration rather than a variable accretion rate. However, three sources showed statistically significant emission line flares in close temporal proximity to very large Fermi γ-ray flares. While we do not have sufficient emission line data to quantitatively assess their correlation with the γ-ray flux, it appears that in some cases the jet might provide additional photoionizing flux to the broad-line region (BLR), which implies that some γ-rays are produced within the BLR, at least for these large flares.

  18. Depletion-mode carrier-plasma optical modulator in zero-change advanced CMOS.

    Science.gov (United States)

    Shainline, Jeffrey M; Orcutt, Jason S; Wade, Mark T; Nammari, Kareem; Moss, Benjamin; Georgas, Michael; Sun, Chen; Ram, Rajeev J; Stojanović, Vladimir; Popović, Miloš A

    2013-08-01

    We demonstrate the first (to the best of our knowledge) depletion-mode carrier-plasma optical modulator fabricated in a standard advanced complementary metal-oxide-semiconductor (CMOS) logic process (45 nm node SOI CMOS) with no process modifications. The zero-change CMOS photonics approach enables this device to be monolithically integrated into state-of-the-art microprocessors and advanced electronics. Because these processes support lateral p-n junctions but not efficient ridge waveguides, we accommodate these constraints with a new type of resonant modulator. It is based on a hybrid microring/disk cavity formed entirely in the sub-90 nm thick monocrystalline silicon transistor body layer. Electrical contact of both polarities is made along the inner radius of the multimode ring cavity via an array of silicon spokes. The spokes connect to p and n regions formed using transistor well implants, which form radially extending lateral junctions that provide index modulation. We show 5 Gbps data modulation at 1265 nm wavelength with 5.2 dB extinction ratio and an estimated 40 fJ/bit energy consumption. Broad thermal tuning is demonstrated across 3.2 THz (18 nm) with an efficiency of 291 GHz/mW. A single postprocessing step to remove the silicon handle wafer was necessary to support low-loss optical confinement in the device layer. This modulator is an important step toward monolithically integrated CMOS photonic interconnects.

  19. GRB hosts through cosmic time. VLT/X-Shooter emission-line spectroscopy of 96 γ-ray-burst-selected galaxies at 0.1

    NARCIS (Netherlands)

    T. Krühler; D. Malesani; J.P.U. Fynbo; O.E. Hartoog; J. Hjorth; P. Jakobsson; D.A. Perley; A.. Rossi; P. Schady; S. Schulze; N.R. Tanvir; S.D. Vergani; K. Wiersema; P.M.J. Afonso; J. Bolmer; Z. Cano; S. Covino; V. D’Elia; A. de Ugarte Postigo; R. Filgas; M. Friis; J.F. Graham; J. Greiner; P. Goldoni; A. Gomboc; F. Hammer; J. Japelj; D.A. Kann; L. Kaper; S. Klose; A.J. Levan; G. Leloudas; B. Milvang-Jensen; A. Nicuesa Guelbenzu; E. Palazzi; E. Pian; S. Piranomonte; R. Sánchez-Ramírez; S. Savaglio; J. Selsing; G. Tagliaferri; P.M. Vreeswijk; D.J. Watson; D. Xu

    2015-01-01

    We present data and initial results from VLT/X-Shooter emission-line spectroscopy of 96 galaxies selected by long γ-ray bursts (GRBs) at 0.1

  20. VERITAS (Venus Emissivity, Radio Science, InSAR, Topo-graphy And Spectroscopy): A Proposed Discovery Mission

    Science.gov (United States)

    Smrekar, Suzanne; Dyar, Melinda; Hensley, Scott; Helbert, Joern; VERITAS Science Team

    2016-10-01

    VERITAS addresses one of the most fundamental questions in planetary evolution: How Earth-like is Venus? These twin planets diverged down different evolutionary paths, yet Venus may hold lessons for past and future Earth, as well as for Earth-sized exoplanets. VERITAS will search for the mineralogical fingerprints of past water, follow up on the discoveries of recent volcanism and the possible young surface age, and reveal the conditions that have prevented plate tectonics from developing. Collectively these questions address how Venus ended up a sulfurous inferno while Earth became habitable.VERITAS carries the Venus Interferometric Synthetic Aperture Radar (VISAR) and the Venus Emissivity Mapper (VEM), plus a gravity science investigation.The VISAR X-band radar produces: 1) a global digital elevation model (DEM) with 250 m postings, 5 m height accuracy, 2) Synthetic aperture radar (SAR) global imaging with 30 m pixels, 3) SAR imaging at 15 m for targeted areas, and 4) surface deformation from repeat pass interferometry (RPI) at 2 mm height precision for targeted, potentially active areas. VEM [see Helbert abstract] will measure surface emissivity, look for active volcanic flows and outgassing of water over ~78% of the surface using 6 NIR surface bands within 5 atmospheric windows and 8 bands for calibration of clouds, stray light, and water vapor.VERITAS uses Ka-band uplink and downlink to create a global gravity field with 3 mgal accuracy and 145 km resolution (130 spherical harmonic degree and order or d&o) and providing a significantly higher resolution field with much more uniform resolution than that available from Magellan.VERITAS will create a rich data set of high resolution topography, imaging, spectroscopy, and gravity. These co-registered data sets will be on par with those acquired for Mercury, Mars and the Moon that have revolutionized our understanding of these bodies. VERITAS would be a valuable asset for future lander or probe missions, collecting

  1. Evaluation of lithium determination in three analyzers: flame emission, flame atomic absorption spectroscopy and ion selective electrode

    Directory of Open Access Journals (Sweden)

    Mehri Aliasgharpour

    2009-10-01

    Full Text Available Background: Lithium carbonate salt has become an increasingly important substance in the treatment of manic depressive disorders, and its relatively narrow therapeutic range has caused laboratories to monitor the serum concentration carefully. In the present work we evaluated lithium measurement in 3 different analyzers. Methods & Materials: Three different analyzers including Flame Emission (FES, Flame Atomic Absorption Spectroscopy (FAAS, and Ion Selective Electrode (ISE were used. All chemicals had a grade suitable for trace metal analysis. Results: Within-day precision of CV was ≤ 1.5% for FES & FAAS, except for ISE (1.9% CV. Between-days precision of CV was less for FES than for FAAS and ISE (1.3% versus 2.2% & 2.3%. The percent recovery of added lithium in pooled patients’ serum was higher for ISE than for FASS and FES (103.4% versus 96.2% and 94.6%. We also obtained a higher average lithium concentration for patients’ serum samples (n=16 measured by ISE than for FAAS and FES (0.825±0.30 versus 0.704±0.26 & 0.735±0.19. Paired t-test results revealed a significant difference (p< 0.001 for patient sera analyzed with FAAS and ISE. Conclusion: We report higher results for ISE than the other two analyzers and conclude that the choice between the two flame methods for patients’ serum lithium determination is arbitrary and that FES analyzer is a more attractive routine alternative for lithium determination than FAAS because of its cost and ease of performance. In addition, the results obtained by ISE are precise. However, its accuracy may depend on other interfering factors.

  2. Atomic emission spectroscopy

    Science.gov (United States)

    Andrew, K. H.

    1975-01-01

    The relationship between the Slater-Condon theory and the conditions within the atom as revealed by experimental data was investigated. The first spectrum of Si, Rb, Cl, Br, I, Ne, Ar, and Xe-136 and the second spectrum of As, Cu, and P were determined. Methods for assessing the phase stability of fringe counting interferometers and the design of an autoranging scanning system for digitizing the output of an infrared spectrometer and recording it on magnetic tape are described.

  3. Issues in deep ocean collinear double-pulse laser induced breakdown spectroscopy: Dependence of emission intensity and inter-pulse delay on solution pressure

    Energy Technology Data Exchange (ETDEWEB)

    Lawrence-Snyder, Marion; Scaffidi, Jonathan P.; Pearman, William F.; Gordon, Christopher M.; Angel, S. Michael

    2014-09-01

    Double-pulse laser-induced breakdown spectroscopy (DP-LIBS) with a collinear laser beam orientation is shown for high-pressure bulk aqueous solutions (up to 50 bar) along with bubble and plasma images. These investigations reveal that the emission plasma is quenched much more rapidly in solution requiring much shorter detector gate delays than for typical LIBS measurements in air. Also, the emission is inversely proportional to solution pressure, and the most intense emission at all pressures occurs when the laser-induced vapor bubble is at a maximum diameter. It is also shown that the laser-induced bubble grows initially at the same rate for all solution pressures, collapsing more quickly as the pressure is increased. Intense emission is best obtained for conditions where the laser-induced bubble formed by the first laser pulse is small and spherically shaped. - Highlights: • Collinear double-pulse LIBS is shown for 50 bar bulk aqueous solutions. • LIBS plasma in solution is much more rapidly quenched than a LIBS plasma in air. • For DP LIBS, the emission is inversely proportional to solution pressure. • Laser-induced bubble growth rate is the same at all solution pressures. • Large spherical laser-induced bubbles produce the strongest DP LIBS emission.

  4. Qualitative tissue differentiation by analysing the intensity ratios of atomic emission lines using laser induced breakdown spectroscopy (LIBS): prospects for a feedback mechanism for surgical laser systems.

    Science.gov (United States)

    Kanawade, Rajesh; Mahari, Fanuel; Klämpfl, Florian; Rohde, Maximilian; Knipfer, Christian; Tangermann-Gerk, Katja; Adler, Werner; Schmidt, Michael; Stelzle, Florian

    2015-01-01

    The research work presented in this paper focuses on qualitative tissue differentiation by monitoring the intensity ratios of atomic emissions using 'Laser Induced Breakdown Spectroscopy' (LIBS) on the plasma plume created during laser tissue ablation. The background of this study is to establish a real time feedback control mechanism for clinical laser surgery systems during the laser ablation process. Ex-vivo domestic pig tissue samples (muscle, fat, nerve and skin) were used in this experiment. Atomic emission intensity ratios were analyzed to find a characteristic spectral line for each tissue. The results showed characteristic elemental emission intensity ratios for the respective tissues. The spectral lines and intensity ratios of these specific elements varied among the different tissue types. The main goal of this study is to qualitatively and precisely identify different tissue types for tissue specific laser surgery. © 2015 The Authors. Journal of Biophotonics published by WILEY-VCH Verlag.

  5. No Thermal Inversion and a Solar Water Abundance for the Hot Jupiter HD209458b from HST WFC3 Emission Spectroscopy

    CERN Document Server

    Line, Michael R; Bean, Jacob; Desert, Jean-Michel; Fortney, Jonathan J; Kreidberg, Laura; Madhusudhan, Nikku; Showman, Adam P; Diamond-Lowe, Hannah

    2016-01-01

    The nature of the vertical thermal structure of hot Jupiter atmospheres is one of the key questions raised by the characterization of transiting exoplanets over the last decade. There have been claims that many hot Jupiter's exhibit vertical profiles with increasing temperature with decreasing pressure in the infrared photosphere that leads to the reversal of molecular absorption bands into emission features (an inversion). However, these claims have been based on broadband photometry rather than the unambiguous identification of emission features with spectroscopy, and the chemical species that could cause the thermal inversions by absorbing stellar irradiation at high altitudes have not been identified despite extensive theoretical and observational effort. Here we present high precision HST WFC3 observations of the dayside emission spectrum of the hot Jupiter HD209458b; the first exoplanet suggested to have a thermal inversion. Our observations resolve a water band in absorption at 6.2 sigma confidence. Wh...

  6. Volcanic SO2 and SiF4 visualization using 2-D thermal emission spectroscopy – Part 1: Slant-columns and their ratios

    Directory of Open Access Journals (Sweden)

    M. Grutter

    2012-02-01

    Full Text Available The composition and emission rates of volcanic gas plumes provide insight of the geologic internal activity, atmospheric chemistry, aerosol formation and radiative processes around it. Observations are necessary for public security and the aviation industry. Ground-based thermal emission infrared spectroscopy, which uses the radiation of the volcanic gas itself, allows for continuously monitoring during day and night from a safe distance. We present measurements on Popocatépetl volcano based on thermal emission spectroscopy during different campaigns between 2006–2009 using a Scanning Infrared Gas Imaging System (SIGIS. The experimental set-up, measurement geometries and analytical algorithms are described. The equipment was operated from a safe distance of 12 km from the volcano at two different spectral resolutions: 0.5 and 4 cm−1. The 2-dimensional scanning capability of the instrument allows for an on-line visualization of the volcanic SO2 plume and its animation. SiF4 was also identified in the infrared spectra recorded at both resolutions. The SiF4/SO2 molecular ratio can be calculated from each image and used as a highly useful parameter to follow changes in volcanic activity. A small Vulcanian eruption was monitored during the night of 16 to 17 November 2008 and strong ash emission together with a pronounced SO2 cloud was registered around 01:00 a.m. LST (Local Standard Time. Enhanced SiF4/SO2 ratios were observed before and after the eruption. A validation of the results from thermal emission measurements with those from absorption spectra of the moon taken at the same time, as well as an error analysis, are presented. The inferred propagation speed from sequential images is used in a subsequent paper (Part 2 to calculate the emission rates at different distances from the crater.

  7. Volcanic SO2 and SiF4 visualization using 2-D thermal emission spectroscopy - Part 1: Slant-columns and their ratios

    Science.gov (United States)

    Stremme, W.; Krueger, A.; Harig, R.; Grutter, M.

    2012-02-01

    The composition and emission rates of volcanic gas plumes provide insight of the geologic internal activity, atmospheric chemistry, aerosol formation and radiative processes around it. Observations are necessary for public security and the aviation industry. Ground-based thermal emission infrared spectroscopy, which uses the radiation of the volcanic gas itself, allows for continuously monitoring during day and night from a safe distance. We present measurements on Popocatépetl volcano based on thermal emission spectroscopy during different campaigns between 2006-2009 using a Scanning Infrared Gas Imaging System (SIGIS). The experimental set-up, measurement geometries and analytical algorithms are described. The equipment was operated from a safe distance of 12 km from the volcano at two different spectral resolutions: 0.5 and 4 cm-1. The 2-dimensional scanning capability of the instrument allows for an on-line visualization of the volcanic SO2 plume and its animation. SiF4 was also identified in the infrared spectra recorded at both resolutions. The SiF4/SO2 molecular ratio can be calculated from each image and used as a highly useful parameter to follow changes in volcanic activity. A small Vulcanian eruption was monitored during the night of 16 to 17 November 2008 and strong ash emission together with a pronounced SO2 cloud was registered around 01:00 a.m. LST (Local Standard Time). Enhanced SiF4/SO2 ratios were observed before and after the eruption. A validation of the results from thermal emission measurements with those from absorption spectra of the moon taken at the same time, as well as an error analysis, are presented. The inferred propagation speed from sequential images is used in a subsequent paper (Part 2) to calculate the emission rates at different distances from the crater.

  8. Evaluation of laser induced breakdown spectroscopy for multielemental determination in soils under sewage sludge application.

    Science.gov (United States)

    Ferreira, Edilene Cristina; Milori, Débora Marcondes Bastos Pereira; Ferreira, Ednaldo José; Dos Santos, Larissa Macedo; Martin-Neto, Ladislau; Nogueira, Ana Rita de Araújo

    2011-07-15

    Laser induced breakdown spectroscopy (LIBS) is an atomic emission spectroscopy technique for simple, direct and clean analysis, with great application potential in environmental sustainability studies. In a single LIBS spectrum it is possible to obtain qualitative information on the sample composition. However, quantitative analysis requires a reliable model for analytical calibration. Multilayer perceptron (MLP), an artificial neural network, is a multivariate technique that is capable of learning to recognize features from examples. Therefore MLP can be used as a calibration model for analytical determinations. Accordingly, the present study proposes to evaluate the traditional linear fit and MLP models for LIBS calibration, in order to attain a quantitative multielemental method for contaminant determination in soil under sewage sludge application. Two sets of samples, both composed of two kinds of soils were used for calibration and validation, respectively. The analyte concentrations in these samples, used as reference, were determined by a reference analytical method using inductively coupled plasma optical emission spectrometry (ICP OES). The LIBS-MLP was compared to a LIBS-linear fit method. The values determined by LIBS-MLP showed lower prediction errors, correlation above 98% with values determined by ICP OES, higher accuracy and precision, lower limits of detection and great application potential in the analysis of different kinds of soils. Copyright © 2011 Elsevier B.V. All rights reserved.

  9. Characterization of metallic nanoparticles by high-resolution X-ray absorption and X-ray emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kuehn, Timna-Josua

    2012-03-15

    In almost all areas of technology, metallic nanoparticles are of interest due to their special thermal, electronic, magnetic and optical properties. Their special properties are mainly due to their small size which implies the relevance of quantum effects as well as the significance of the surface: For 2 nm nanoparticles, the surface-to-volume ratio is already 1:1. However, the identification of surface-to-volume interactions - that are responsible for the new properties - is a difficult task due to the small size that inhibits a lot of 'standard' techniques to be applicable. Here X-ray absorption/emission spectroscopy (XAS/XES) is a favorable tool for the characterization of nanoparticles, independent on size, degree of crystallinity and shape/condition of the surface. Using XAS, a tempered nanosized Co{sub 3}Pt/C catalyst have been investigated. Its outstanding oxygen-reduction reaction (ORR) properties in a fuel cell could be related to a lowered Pt 5d-band center connected to a tightened Pt-Pt bonding distance, leading to a weakening of the oxygen adsorption strength so that the ORR may proceed faster. One drawback remains, however, as the properties found by (standard) XAS are summed up for different chemical environments of the chosen element. Thus, no distinction can be made between, e.g., the pure metal in a nanoparticles' interior and the ligated metal in the outer shells or surface. Here, high-resolution fluorescence-detected XAS (HRFD-XAS) provides additional opportunities as, due to its chemical sensitivity, it leads to site-selective XAS. For a system of 6 nm sized Co nanoparticles, build up of a metallic core surrounded by a protecting shell, that resulted from the 'smooth oxidation' process, this technique of site-selective XAS was proven to be applicable. For the first time, the interior and outer shell of a metallic nanoparticle could be characterized separately. In particular, the Co-hcp phase could be determined for the

  10. The Grism Lens-Amplified Survey from Space (GLASS). III. A census of Ly\\alpha\\ Emission at $z\\gtrsim$7 from HST Spectroscopy

    CERN Document Server

    Schmidt, K B; Bradač, M; Vulcani, B; Huang, K -H; Hoag, A; Maseda, M; Guaita, L; Pentericci, L; Brammer, G B; Dijkstra, M; Dressler, A; Fontana, A; Henry, A L; Jones, T A; Mason, C; Trenti, M; Wang, X

    2015-01-01

    [abbreviated] We present a census of Ly\\alpha\\ emission at $z\\gtrsim7$ utilizing deep near infrared HST grism spectroscopy from the first six completed clusters of the Grism Lens-Amplified Survey from Space (GLASS). In 24/159 photometrically selected galaxies we detect emission lines consistent with Ly\\alpha\\ in the GLASS spectra. Based on the distribution of signal-to-noise ratios and on simulations we expect the completeness and the purity of the sample to be 40-100% and 60-90%, respectively. For the objects without detected emission lines we show that the observed (not corrected for lensing magnification) 1$\\sigma$ flux limits reaches $5\\times10^{-18}$erg/s/cm$^{2}$ per position angle over the full wavelength range of GLASS (0.8-1.7$\\mu$m). Based on the conditional probability of Ly\\alpha\\ emission measured from the ground at $z\\sim7$ we would have expected 12-18 Ly\\alpha\\ emitters. This is consistent with the number of detections, within the uncertainties, confirming the drop in Ly\\alpha\\ emission with re...

  11. Simple and Precise Quantification of Iron Catalyst Content in Carbon Nanotubes Using UV/Visible Spectroscopy.

    Science.gov (United States)

    Agustina, Elsye; Goak, Jeungchoon; Lee, Suntae; Seo, Youngho; Park, Jun-Young; Lee, Naesung

    2015-10-01

    Iron catalysts have been used widely for the mass production of carbon nanotubes (CNTs) with high yield. In this study, UV/visible spectroscopy was used to determine the Fe catalyst content in CNTs using a colorimetric technique. Fe ions in solution form red-orange complexes with 1,10-phenanthroline, producing an absorption peak at λ=510 nm, the intensity of which is proportional to the solution Fe concentration. A series of standard Fe solutions were formulated to establish the relationship between optical absorbance and Fe concentration. Many Fe catalysts were microscopically observed to be encased by graphitic layers, thus preventing their extraction. Fe catalyst dissolution from CNTs was investigated with various single and mixed acids, and Fe concentration was found to be highest with CNTs being held at reflux in HClO4/HNO3 and H2SO4/HNO3 mixtures. This novel colorimetric method to measure Fe concentrations by UV/Vis spectroscopy was validated by inductively coupled plasma optical emission spectroscopy, indicating its reliability and applicability to asses Fe content in CNTs.

  12. VLT/XSHOOTER & Subaru/MOIRCS Spectroscopy of HUDF-YD3: No Evidence for Lyman-alpha Emission at z=8.55

    CERN Document Server

    Bunker, Andrew J; Wilkins, Stephen M; Stanway, Elizabeth R; Lorenzoni, Silvio; Lacy, Mark; Jarvis, Matt J; Hickey, Samantha

    2013-01-01

    We present spectroscopic observations with VLT/XSHOOTER and Subaru/MOIRCS of a relatively bright Y-band drop-out galaxy in the Hubble Ultra Deep Field, first selected by Bunker et al. (2010), McLure et al. (2010) and Bouwens et al. (2010) to be a likely z~8-9 galaxy on the basis of its colours in the HST ACS and WFC3 images. This galaxy, HUDF.YD3 (also known as UDFy-38135539) has been targetted for VLT/SINFONI integral field spectroscopy by Lehnert et al. (2010), who published a candidate Lyman-alpha emission line at z=8.55 from this source. In our independent spectroscopy using two different infrared spectrographs (5 hours with VLT/XSHOOTER and 11 hours with Subaru/MOIRCS) we are unable to reproduce this line. We do not detect any emission line at the spectral and spatial location reported in Lehnert et al. (2010), despite the expected signal in our combined MOIRCS & XSHOOTER data being 5-sigma. The line emission also seems to be ruled out by the faintness of this object in recently extremely deep F105W ...

  13. Soft X-ray emission spectroscopy used for the characterization of a-C and CN{sub x} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Nepijko, S.A., E-mail: nepijko@uni-mainz.de [Institute of Physics, University of Mainz, Staudingerweg 7, 55128 Mainz (Germany); Chernenkaya, A. [Institute of Physics, University of Mainz, Staudingerweg 7, 55128 Mainz (Germany); Graduate School Materials Science in Mainz, Staudingerweg 9, 55128 Mainz (Germany); Medjanik, K.; Chernov, S.V. [Institute of Physics, University of Mainz, Staudingerweg 7, 55128 Mainz (Germany); Klimenkov, M. [Institute for Applied Materials, Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Vlasenko, O.V. [Sumy State University, Rimsky-Korsakov str. 2, 40007 Sumy (Ukraine); Petrovskaya, S.S. [Frantsevich Institute for Problems of Materials Science, National Academy of Sciences of Ukraine, Krzhizhanovsky str. 3, 03142 Kiev (Ukraine); Odnodvorets, L.V. [Sumy State University, Rimsky-Korsakov str. 2, 40007 Sumy (Ukraine); Zaulichnyy, Ya.V. [National Technical University of Ukraine (KPI), Pobedy Av. 37, 03056 Kiev (Ukraine); Schönhense, G. [Institute of Physics, University of Mainz, Staudingerweg 7, 55128 Mainz (Germany)

    2015-02-27

    We present the results of a soft X-ray emission spectroscopy study of a-C and CN{sub x} films on a Si(100) substrate. Also for the characterization of the homogeneity in depth of these films electron energy loss spectroscopy measurements with localization better than 4 nm were carried out. In case of CN{sub x} films the highest diamond-like modification occurs in the region close to the Si(100) substrate. The film density decreases with increasing distance from the substrate and becomes almost constant in range of thicknesses more than ~ 2 nm. - Highlights: • CN{sub x} and a-C film densities decrease with the increase of thickness. • Density increases with the decrease of Si(100) substrate temperature at preparation. • Highest concentration of the diamond-like structure is in the substrate vicinity. • It reduces further from the substrate and stabilizes at thickness ≥ 2 nm.

  14. Optimization of digestion parameters for analysing the total sulphur of mine tailings by inductively coupled plasma optical emission spectrometry.

    Science.gov (United States)

    Alam, Raquibul; Shang, Julie Q; Cheng, Xiangrong

    2012-05-01

    The oxidation of sulphidic mine tailings and consequent acid generation poses challenges for the environment. Accurate and precise analysis of sulphur content is necessary for impact assessment and management of mine tailings. Here, the authors aim at developing a rapid and easy digestion procedure, which may analyse and measure the total amount of sulphur in mine tailings by using inductively coupled plasma. For evaluating effects of several variables, the researchers used a univariate (analysis of variance (ANOVA)) strategy and considered factors such as composition of the acid mixture, heating time, and refluxing device to optimize the performance. To do the experiment, the researchers have used two certified reference materials (KZK-1 and RTS-2) and samples of tailings from Musselwhite mine. ANOVA result shows that heating time is the most influencing factor on acid digestion of the reference materials whereas in case of a digestion of tailings sample, hydrochloric acid proved to be the most significant parameter. Satisfactory results between the measured and referenced values are found for all experiments. It is found that the aqua regia (1 ml HNO(3) + 3 ml HCl) digestion of 0.1 g of samples after only 40 min of heating at 95°C produced fast, safe, and accurate analytical results with a recovery of 97% for the selected reference materials.

  15. Simultaneous determination of hydride and non-hydride forming elements by inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Benzo, Z. [Instituto Venezolano de Investigaciones Cientificas, IVIC, Altos de Pipe, Caracas (Venezuela, Bolivarian Republic of); Matos-Reyes, M.N.; Cervera, M.L.; Guardia, M. de la, E-mail: m.luisa.cervera@uv.es [Department of Analytical Chemistry, University of Valencia, Valencia (Spain)

    2011-09-15

    The operating characteristics of a dual nebulization system were studied including instrumental and chemical conditions for the hydride generation and analytical figures of merit for both, hydride and non hydride forming elements. Analytical performance of the nebulization system was characterized by detection limits from 0.002 to 0.0026 {mu}g mL{sup -1} for the hydride forming elements and between 0.0034 and 0.0121 {mu}g mL{sup -1} for the non-hydride forming elements, relative standard deviation for 10 replicate measurements at 0.25 mg L{sup -1} level and recovery percentages between 97 and 103%. The feasibility of the system was demonstrated in the simultaneous determination of Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Mo, Ni, Zn, As, Bi, Sb, Se, and Te in the NIST 1549 (non-fat milk powder), NIST 1570a (spinach leaves), DORM-2 (dogfish muscle) and TORT-2 (lobster hepatopancreas) certified samples for trace elements. Results found were in good agreement with the certified ones. (author)

  16. Field-flow fractionation: An efficient approach for matrix removal of soil extract for inductively coupled plasma optical emission spectrometry

    Science.gov (United States)

    Sangsawong, Supharart; Waiyawat, Weerawan; Shiowatana, Juwadee; Siripinyanond, Atitaya

    2011-06-01

    An on-line coupling between a continuous-flow sequential extraction (CFSE) unit and flow field-flow fractionation with cross flow matrix removal (FlFFF/CFM) with ICP-OES detection was developed for determination of metal leachability from soil. The use of high concentration of Mg(NO 3) 2 in exchangeable phase can cause undesirable matrix effects by shifting ionization equilibrium in the plasma, etc., resulting in a clear need for matrix removal. Therefore, the capability of FlFFF/CFM to remove Mg matrix ion from soil extract was evaluated. Poly(ethylene imine) (PEI) having molecular weight of 25,000 Da was added to form complexes with analyte elements (Cu, Mn, Pb, and Zn) but not the matrix element (Mg). The free Mg matrix ions were then removed by filtering off through the ultrafiltration membrane, having a 1000-Da molecular weight cut-off, inside the FlFFF channel. With the use of FlFFF/CFM, matrix removal efficiency was approximately 83.5%, which was equivalent to approximately 6-fold dilution of the matrix ion. The proposed hyphenated system of CFSE and FlFFF/CFM with ICP-OES detection was examined for its reliability by checking with SRM 2710 (a highly contaminated soil from Montana). The metal contents determined by the proposed method were not significantly different (at 95% confidence) from the certified values.

  17. ESTIMATION OF METHANE EMISSIONS FROM A SURFACE COAL MINE USING OPEN-PATH FTIR SPECTROSCOPY AND MODELING TECHNIQUES

    Science.gov (United States)

    A new measurements methodology has been developed which allows the rapid and efficient measurement of methane (CH4) emissions from surface coal mines. An initial field trial of this methodology has been completed, and results from the field trial revealed that emissions from one ...

  18. LASER ABLATION-INDUCTIVELY COUPLED PLASMA-ATOMIC EMISSION SPECTROSCOPY STUDY AT THE 222-S LABORATORY USING HOT-CELL GLOVE BOX PROTOTYPE SYSTEM

    Energy Technology Data Exchange (ETDEWEB)

    SEIDEL CM; JAIN J; OWENS JW

    2009-02-23

    This report describes the installation, testing, and acceptance of the Waste Treatment and Immobilization Plant (WTP) procured laser ablation-inductively coupled plasma-atomic emission spectroscopy (LA-ICP-AES) system for remotely analyzing high-level waste (HLW) samples in a hot cell environment. The work was completed by the Analytical Process Development (APD) group in accordance with Task Order 2005-003; ATS MP 1027, Management Plan for Waste Treatment Plant Project Work Performed by Analytical Technical Services. The APD group at the 222-S Laboratory demonstrated acceptable turnaround time (TAT) and provide sufficient data to assess sensitivity, accuracy, and precision of the LA-ICP-AES method.

  19. Noninvasive express diagnostics of pulmonary diseases based on control of patient's gas emission using methods of IR and terahertz laser spectroscopy

    Science.gov (United States)

    Starikova, M. K.; Bulanova, A. A.; Bukreeva, E. B.; Karapuzikov, A. A.; Karapuzikov, A. I.; Kistenev, Y. V.; Klementyev, V. M.; Kolker, D. B.; Kuzmin, D. A.; Nikiforova, O. Y.; Ponomarev, Yu. N.; Sherstov, I. V.; Boyko, A. A.

    2013-11-01

    Pulmonary diseases diagnostics always occupies one of the key positions in medicine practices. A large variety of high technology methods are used today, but none of them cannot be used for early screening of pulmonary diseases. We discuss abilities of methods of IR and terahertz laser spectroscopy for noninvasive express diagnostics of pulmonary diseases on a base of analysis of absorption spectra of patient's gas emission, in particular, exhaled air. Experience in the field of approaches to experimental data analysis and hard-ware realization of gas analyzers for medical applications is also discussed.

  20. Infrared heterodyne spectroscopy of astronomical and laboratory sources at 8.5 micron. [absorption line profiles of nitrogen oxide and black body emission from Moon and Mars

    Science.gov (United States)

    Mumma, M.; Kostiuk, T.; Cohen, S.; Buhl, D.; Vonthuna, P. C.

    1974-01-01

    The first infrared heterodyne spectrometer using tuneable semiconductor (PbSe) diode lasers has been constructed and was used near 8.5 micron to measure absorption line profiles of N2O in the laboratory and black body emission from the Moon and from Mars. Spectral information was recorded over a 200 MHz bandwidth using an 8-channel filter bank. The resolution was 25 MHz and the minimum detectable (black body) power was 1 x 10 to the minus 16th power watts for 8 minutes of integration. The results demonstrate the usefulness of heterodyne spectroscopy for the study of remote and local sources in the infrared.

  1. Simulating Valence-to-Core X-ray Emission Spectroscopy of Transition Metal Complexes with Time-Dependent Density Functional Theory

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yu; Mukamel, Shaul; Khalil, Munira; Govind, Niranjan

    2015-11-09

    Valence-to-core (VtC) X-ray emission spectroscopy (XES) has emerged as a power- ful technique for the structural characterization of complex organometallic compounds in realistic environments. Since the spectrum represents electronic transitions from the ligand molecular orbitals to the core holes of the metal centers, the approach is more chemically sensitive to the metal-ligand bonding character compared with con- ventional X-ray absorption techniques. In this paper we study how linear-response time-dependent density functional theory (LR-TDDFT) can be harnessed to simulate K-edge VtC X-ray emission spectra reliably. LR-TDDFT allows one to go beyond the single-particle picture that has been extensively used to simulate VtC-XES. We con- sider seven low- and high-spin model complexes involving chromium, manganese and iron transition metal centers. Our results are in good agreement with experiment.

  2. Controlled variation of the information depth by angle dependent soft X-ray emission spectroscopy: A study on polycrystalline Cu(In,Ga)Se 2

    Science.gov (United States)

    Mönig, H.; Lauermann, I.; Grimm, A.; Camus, C.; Kaufmann, C. A.; Pistor, P.; Jung, Ch.; Kropp, T.; Lux-Steiner, M. C.; Fischer, Ch.-H.

    2008-12-01

    Angle dependent X-ray emission spectroscopy (AXES) is introduced as a tool for depth dependent composition analysis. A controlled variation of the information depth is demonstrated by changing the geometry from grazing exit to grazing incidence geometry. First results are presented from Cu(In,Ga)Se 2 (CIGSe)-based polycrystalline thin film solar cell bi-layer components. A mathematical model explains changes in relative intensity due to the absorption and emission behavior of thin CdS and Zn(S,O) cover layers. The fact that the presented data can be modelled by ideal bi-layer structures, provides both, proof of concept in general and the proof of applicability to the relatively rough layered structures based on CIGSe. In bare CIGSe a homogeneous distribution of Cu and Ga is found in a depth range between 22 and 470 nm.

  3. Determination of nitrous acid emission factors from a gasoline vehicle using a chassis dynamometer combined with incoherent broadband cavity-enhanced absorption spectroscopy.

    Science.gov (United States)

    Nakashima, Yoshihiro; Kajii, Yoshizumi

    2017-01-01

    Nitrous acid (HONO) is a well-known source of hydroxyl radicals in the troposphere. Vehicle exhaust is considered to be one of the primary emission sources of HONO. In this study, measurements of HONO in gasoline vehicle exhaust were carried out using a chassis dynamometer combined with incoherent broadband cavity-enhanced absorption spectroscopy. When catalysts were warm, concentrations of HONO were higher than those prior to catalysts warming. Other species, such as CO, and total hydrocarbons (THCs), showed the opposite pattern. There were no correlations evident between HONO and other trace species concentrations immediately after emission. The HONO/NOx ratio, a good proxy for the formation of HONO in atmosphere, ranged from 1.1 to 6.8×10(-3), which was consistent with previous studies. HONO emission factors (EFs) were calculated to be 0.01-3.6mgkg(-1) fuel, which was different from the vehicle's specifications and those reported under different driving cycles. Annual HONO emissions in Japan were estimated using the calculated EFs and other statistical data. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. The Number Density Evolution of Extreme Emission Line Galaxies in 3D-HST: Results from a Novel Automated Line Search Technique for Slitless Spectroscopy

    CERN Document Server

    Maseda, Michael V; Rix, Hans-Walter; Momcheva, Ivelina; Brammer, Gabriel B; Franx, Marijn; Lundgren, Britt F; Skelton, Rosalind E; Whitaker, Katherine E

    2016-01-01

    The multiplexing capability of slitless spectroscopy is a powerful asset in creating large spectroscopic datasets, but issues such as spectral confusion make the interpretation of the data challenging. Here we present a new method to search for emission lines in the slitless spectroscopic data from the 3D-HST survey utilizing the Wide-Field Camera 3 on board the Hubble Space Telescope. Using a novel statistical technique, we can detect compact (extended) emission lines at 90% completeness down to fluxes of 1.5 (3.0) times 10^{-17} erg/s/cm^2, close to the noise level of the grism exposures, for objects detected in the deep ancillary photometric data. Unlike previous methods, the Bayesian nature allows for probabilistic line identifications, namely redshift estimates, based on secondary emission line detections and/or photometric redshift priors. As a first application, we measure the comoving number density of Extreme Emission Line Galaxies (restframe [O III] 5007 equivalent widths in excess of 500 Angstroms)...

  5. Remote sensing of temperature and concentration profiles of a gas jet by coupling infrared emission spectroscopy and LIDAR for characterization of aircraft engine exhaust

    Science.gov (United States)

    Offret, J.-P.; Lebedinsky, J.; Navello, L.; Pina, V.; Serio, B.; Bailly, Y.; Hervé, P.

    2015-05-01

    Temperature data play an important role in the combustion chamber since it determines both the efficiency and the rate of pollutants emission of engines. Air pollution problem concerns the emissions of gases such as CO, CO2, NO, NO2, SO2 and also aerosols, soot and volatile organic compounds. Flame combustion occurs in hostile environments where temperature and concentration profiles are often not easy to measure. In this study, a temperature and CO2 concentration profiles optical measurement method, suitable for combustion analysis, is discussed and presented. The proposed optical metrology method presents numerous advantages when compared to intrusive methods. The experimental setup comprises a passive radiative emission measurement method combined with an active laser-measurement method. The passive method is based on the use of gas emission spectroscopy. The experimental spectrometer device is coupled with an active method. The active method is used to investigate and correct complex flame profiles. This method similar to a LIDAR (Light Detection And Ranging) device is based on the measurement of Rayleigh scattering of a short laser pulse recorded using a high-speed streak camera. The whole experimental system of this new method is presented. Results obtained on a small-scale turbojet are shown and discussed in order to illustrate the potentials deliver by the sophisticated method. Both temperature and concentration profiles of the gas jet are presented and discussed.

  6. AKARI near-infrared spectroscopy of the extended green object G318.05+0.09: Detection of CO fundamental ro-vibrational emission

    CERN Document Server

    Onaka, Takashi; Sakon, Itsuki; Ardaseva, Aleksandra

    2016-01-01

    We present the results of near-infrared (2.5--5.4um) long-slit spectroscopy of the extended green object (EGO) G318.05+0.09 with AKARI. Two distinct sources are found in the slit. The brighter source has strong red continuum emission with H2O ice, CO2 ice, and CO gas and ice absorption features at 3.0, 4.25um, 4.67um, respectively, while the other greenish object shows peculiar emission that has double peaks at around 4.5 and 4.7um. The former source is located close to the ultra compact HII region IRAS 14498-5856 and is identified as an embedded massive young stellar object. The spectrum of the latter source can be interpreted by blue-shifted (-3000 ~ -6000km/s) optically-thin emission of the fundamental ro-vibrational transitions (v=1-0) of CO molecules with temperatures of 12000--3700K without noticeable H2 and HI emission. We discuss the nature of this source in terms of outflow associated with the young stellar object and supernova ejecta associated with a supernova remnant.

  7. Quantification of fluorine traces in solid samples using CaF molecular emission bands in atmospheric air Laser-Induced Breakdown Spectroscopy

    Science.gov (United States)

    Alvarez-Llamas, C.; Pisonero, J.; Bordel, N.

    2016-09-01

    Direct solid determination of trace amounts of fluorine using Laser-Induced Breakdown Spectroscopy (LIBS) is a challenging task due to the low excitation efficiency of this element. Several strategies have been developed to improve the detection capabilities, including the use of LIBS in a He atmosphere to enhance the signal to background ratios of F atomic emission lines. An alternative method is based on the detection of the molecular compounds that are formed with fluorine in the LIBS plasma. In this work, the detection of CaF molecular emission bands is investigated to improve the analytical capabilities of atmospheric air LIBS for the determination of fluorine traces in solid samples. In particular, Cu matrix samples containing different fluorine concentration (between 50 and 600 μg/g), and variable amounts of Ca, are used to demonstrate the linear relationships between CaF emission signal and F concentration. Limits of detection for fluorine are improved by more than 1 order of magnitude using CaF emission bands versus F atomic lines, in atmospheric-air LIBS. Furthermore, a toothpaste powder sample is used to validate this analytical method. Good agreement is observed between the nominal and the predicted fluorine mass-content.

  8. Heterogeneity in optical properties of near white-light emissive europium complex species revealed by spectroscopy of single nanoaggregates

    Science.gov (United States)

    Irfanullah, Mir; Sharma, Dharmendar Kumar; Chulliyil, Ramya; Layek, Arunasish; De, Suman; Chowdhury, Arindam

    2017-01-01

    Photoluminescence microscopy has been used to interrogate individual nanoaggregates (NAs) of visible light excitable Eu(III)-complex species with 9-hydroxyphenalenone which we found to emit near-white light in methanol. In the solid state however, NAs display diverse emission spectra due to varied sensitization efficiencies, and thereby exhibit a wide range of emission colours. Heterogeneity in sensitization efficiency and asymmetry ratios for Eu-emission is intriguing because all measurable photoluminescence parameters are expected to average out over large number of Eu-complex species which constitute NAs, and suggests the existence of relatively few yet efficient Eu3+ radiative trap centres of varied asymmetry within NAs.

  9. Study on Emission Spectral Lines of Iron, Fe in Laser-Induced Breakdown Spectroscopy (LIBS) on Soil Samples

    Science.gov (United States)

    Idris, Nasrullah; Lahna, Kurnia; Fadhli; Ramli, Muliadi

    2017-05-01

    In this work, LIBS technique has been used for detection of heavy metal especially iron, Fe in soil sample. As there are a large number of emission spectral lines due to Fe and other constituents in soil, this study is intended to identify emission spectral lines of Fe and finally to find best fit emission spectral lines for carrying out a qualitative and quantitative analysis. LIBS apparatus used in this work consists of a laser system (Neodymium Yttrium Aluminum Garnet, Nd-YAG: Quanta Ray; LAB SERIES; 1,064 nm; 500 mJ; 8 ns) and an optical multichannel analyzer (OMA) system consisting of a spectrograph (McPherson model 2061; 1,000 mm focal length; f/8.6 Czerny- Turner) and an intensified charge coupled device (ICCD) 1024x256 pixels (Andor I*Star). The soil sample was collected from Banda Aceh city, Aceh, Indonesia. For spectral data acquisition, the soil sample has been prepared by a pressing machine in the form of pellet. The laser beam was focused using a high density lens (f=+150 mm) and irradiated on the surface of the pellet for generating luminous plasma under 1 atmosphere of air surrounding. The plasma emission was collected by an optical fiber and then sent to the optical multichannel analyzer (OMA) system for acquisition of the emission spectra. It was found that there are many Fe emission lines both atomic lines (Fe I) and ionic lines (Fe II) appeared in all detection windows in the wavelength regions, ranging from 200 nm to 1000 nm. The emission lines of Fe with strong intensities occurs together with emission lines due to other atoms such as Mg, Ca, and Si. Thus, the identification of emission lines from Fe is complicated by presence of many other lines due to other major and minor elements in soil. Considering the features of the detected emission lines, several emission spectral lines of Fe I (atomic emission line), especially Fe I 404.58 nm occurring at visible range are potential to be good candidate of analytical lines in relation to detection

  10. Investigation of biodistribution behavior of platinum particles in mice: Correlation between inductively coupled plasma-atomic emission spectroscopy and X-ray scanning analytical microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Abe, Shigeaki, E-mail: sabe@den.hokudai.ac.jp [Graduate School of Dental Medicine, Hokkaido University, Sapporo (Japan); Koyama, Chika; Mutoh, Mami [Faculty of Dental Medicine, Hokkaido University, Sapporo (Japan); Akasaka, Tsukasa [Graduate School of Dental Medicine, Hokkaido University, Sapporo (Japan); Uo, Motohiro [Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo (Japan); Watari, Fumio [Graduate School of Dental Medicine, Hokkaido University, Sapporo (Japan)

    2012-12-01

    Highlights: Black-Right-Pointing-Pointer We investigated the biodistribution of platinum microparticles in mice. Black-Right-Pointing-Pointer The biodistribution behavior was observed using inductively coupled plasma-atomic emission spectroscopy (ICP) and scanning X-ray analytical microscopy (XSAM). Black-Right-Pointing-Pointer The administered particles quickly reached in spleen, liver and lung with constant ration. Black-Right-Pointing-Pointer We also estimated the correlation ship between XSAM and ICP measurement. Black-Right-Pointing-Pointer The relative ratio of XSAM intensity showed highly correlation with the relative ratio of Pt concentration in organs. - Abstract: In this study, we investigated the biodistribution of platinum (Pt) microparticles in mice. The particles were administered through the tail vein, and then the biodistribution behavior was observed using inductively coupled plasma-atomic emission spectroscopy (ICP) and scanning X-ray analytical microscopy (XSAM). The administered particles quickly reached the spleen, liver, and lung at a constant ratio, and the ratio remained constant for four weeks. We also estimated the correlation between XSAM and ICP measurement. The relative ratio of XSAM intensity showed strong correlation with the relative ratio of Pt concentration in organs.

  11. Evaluation of Optical Depths and Self-Absorption of Strontium and Aluminum Emission Lines in Laser-Induced Breakdown Spectroscopy (LIBS).

    Science.gov (United States)

    Alfarraj, Bader A; Bhatt, Chet R; Yueh, Fang Yu; Singh, Jagdish P

    2017-04-01

    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 [Formula: see text] (the number density N and the absorption path length [Formula: see text]) 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 laser energy, 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.

  12. Measurements of plasma temperature and electron density in laser-induced copper plasma by time-resolved spectroscopy of neutral atom and ion emissions

    Indian Academy of Sciences (India)

    V K Unnikrishnan; Kamlesh Alti; V B Kartha; C Santhosh; G P Gupta; B M Suri

    2010-06-01

    Plasma produced by a 355 nm pulsed Nd:YAG laser with a pulse duration of 6 ns focussed onto a copper solid sample in air at atmospheric pressure is studied spectroscopically. The temperature and electron density characterizing the plasma are measured by time-resolved spectroscopy of neutral atom and ion line emissions in the time window of 300–2000 ns. An echelle spectrograph coupled with a gated intensified charge coupled detector is used to record the plasma emissions. The temperature is obtained using the Boltzmann plot method and the electron density is determined using the Saha– Boltzmann equation method. Both parameters are studied as a function of delay time with respect to the onset of the laser pulse. The results are discussed. The time window where the plasma is optically thin and is also in local thermodynamic equilibrium (LTE), necessary for the laser-induced breakdown spectroscopy (LIBS) analysis of samples, is deduced from the temporal evolution of the intensity ratio of two Cu I lines. It is found to be 700–1000 ns.

  13. GRB hosts through cosmic time - VLT/X-shooter emission-line spectroscopy of 96 GRB-selected galaxies at 0.1 < z < 3.6

    CERN Document Server

    Krühler, T; Fynbo, J P U; Hartoog, O E; Hjorth, J; Jakobsson, P; Perley, D A; Rossi, A; Schady, P; Schulze, S; Tanvir, N R; Vergani, S D; Wiersema, K; Afonso, P M J; Bolmer, J; Cano, Z; Covino, S; D'Elia, V; Postigo, A de Ugarte; Filgas, R; Friis, M; Graham, J F; Greiner, J; Goldoni, P; Gomboc, A; Hammer, F; Japelj, J; Kann, D A; Kaper, L; Klose, S; Levan, A J; Leloudas, G; Milvang-Jensen, B; Guelbenzu, A Nicuesa; Palazzi, E; Pian, E; Piranomonte, S; Sanchez-Ramirez, R; Savaglio, S; Selsing, J; Tagliaferri, G; Vreeswijk, P M; Watson, D J; Xu, D

    2015-01-01

    We present data and initial results from VLT/X-shooter emission-line spectroscopy of 96 GRB-selected galaxies at 0.1spectroscopy available to date. The majority of our GRBs was detected by Swift and 76% are at 0.5emission-line widths (sigma). We find a strong change of the typical physical properties of GRB hosts with redshift. The median SFR, for example, increases from ~0.6 M_sun/yr at z~0.6 up to ~15 M_sun/yr at z~2. A higher ratio of [OIII]/[OII] at higher redshifts leads to an increasing distance of GRB-selected galaxies to the locus of local galaxies in the BPT diagram. Oxygen abundances of the galaxies are distributed between 12+log(O/H)=7.9 and 12+log(O/H)=9.0 with a median of 12+log(O/H)~8.5. The fraction of GRB-selected galaxies with super-solar metallic...

  14. Optical emission spectroscopy study of the expansion dynamics of a laser generated plasma during the deposition of thin films by laser ablation

    Directory of Open Access Journals (Sweden)

    Fazio, Enza

    2007-09-01

    Full Text Available The dynamics of the expanding plasma produced by excimer laser ablation of different materials such as silicon, silicon carbide, graphite and tin powder were studied by means of time integrated, spatially resolved emission spectroscopy and fast photography imaging of the expanding plasma. Experiments were performed both in vacuum and in different pure background atmosphere (i.e. oxygen or nitrogen and, finally, in gaseous mixtures (i.e. in O2/Ar and N2/Ar mixtures. These investigations were performed to gather information on the nature of the chemical species present in the plasma and on the occurrence of chemical reactions during the interaction between the plasma and the background gas. Then, we tried to correlate the plasma expansion dynamics to the structural and physical properties of the deposited materials. Experimental results clearly indicate that there is a strong correlation between the plasma expansion dynamics and the structural properties of the deposited thin films. In this respect, the investigations performed by means of fast photography and of optical emission spectroscopy revealed themselves as powerful tools for an efficient control of the deposition process itself.

  15. Calibration-free quantitative analysis of elemental ratios in intermetallic nanoalloys and nanocomposites using Laser Induced Breakdown Spectroscopy (LIBS).

    Science.gov (United States)

    Davari, Seyyed Ali; Hu, Sheng; Mukherjee, Dibyendu

    2017-03-01

    Intermetallic nanoalloys (NAs) and nanocomposites (NCs) have increasingly gained prominence as efficient catalytic materials in electrochemical energy conversion and storage systems. But their morphology and chemical compositions play critical role in tuning their catalytic activities, and precious metal contents. While advanced microscopy techniques facilitate morphological characterizations, traditional chemical characterizations are either qualitative or extremely involved. In this study, we apply Laser Induced Breakdown Spectroscopy (LIBS) for quantitative compositional analysis of NAs and NCs synthesized with varied elemental ratios by our in-house built pulsed laser ablation technique. Specifically, elemental ratios of binary PtNi, PdCo (NAs) and PtCo (NCs) of different compositions are determined from LIBS measurements employing an internal calibration scheme using the bulk matrix species as internal standards. Morphology and qualitative elemental compositions of the aforesaid NAs and NCs are confirmed from Transmission Electron Microscopy (TEM) images and Energy Dispersive X-ray Spectroscopy (EDX) measurements. LIBS experiments are carried out in ambient conditions with the NA and NC samples drop cast on silicon wafers after centrifugation to increase their concentrations. The technique does not call for cumbersome sample preparations including acid digestions and external calibration standards commonly required in Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES) techniques. Yet the quantitative LIBS results are in good agreement with the results from ICP-OES measurements. Our results indicate the feasibility of using LIBS in future for rapid and in-situ quantitative chemical characterizations of wide classes of synthesized NAs and NCs.

  16. Laser-induced breakdown spectroscopy application to control of the process of precious metal recovery and recycling

    Energy Technology Data Exchange (ETDEWEB)

    Legnaioli, S.; Lorenzetti, G.; Pardini, L. [Institute of Chemistry of Organometallic Compounds, Research Area of CNR, Via G. Moruzzi, 1-56124 Pisa (Italy); Palleschi, V., E-mail: vincenzo.palleschi@cnr.it [Institute of Chemistry of Organometallic Compounds, Research Area of CNR, Via G. Moruzzi, 1-56124 Pisa (Italy); Pace, D.M. Diaz [Instituto de Fisica ' Arroyo Seco' , Facultad de Ciencias Exactas, Paraje Arroyo Seco-(B7000GHG) Tandil (Argentina); Garcia, F. Anabitarte [Photonic Engineering Group, Universidad de Cantabria, Edificio I-D-i Telecomunicacion, Dpto. TEISA-39005 Santander (Spain); Grassi, R.; Sorrentino, F.; Carelli, G.; Francesconi, M.; Francesconi, F. [Marwan Technology, Largo Pontecorvo, 3-56127 Pisa Italy (Italy); Borgogni, R. [CABRO S.p.A.,Via Setteponti, 141-52100 Arezzo (Italy)

    2012-05-15

    In this paper, we discuss the application of laser-induced breakdown spectroscopy to precious metal alloys used for the control of the process of recovery and recycling of scraps and waste of industrial processes. In particular, the possibility to obtain sensitivity and trueness comparable to the current systems used in industrial environment in the quantitative determination of the elements of interest was explored. The present study demonstrates that laser-induced breakdown spectroscopy can be considered as a viable alternative to inductively coupled plasma optical emission spectrometry and X-ray fluorescence spectroscopy for the determination of recovered precious metals. The limits of detection obtained are of the order of 0.2 mg/g for all the elements considered. The maximum deviation with respect to the nominal concentrations is around 1 mg/g at concentrations around 20 mg/g (gold) corresponding to a relative error slightly higher than {+-} 5%. - Highlights: Black-Right-Pointing-Pointer We discuss application of LIBS for the analysis of recovered precious metals. Black-Right-Pointing-Pointer The advantages and drawbacks of LIBS vs. XRF are evidenced. Black-Right-Pointing-Pointer A strategy is devised for obtaining by LIBS limits of detection comparable to XRF. Black-Right-Pointing-Pointer The same strategy would provide trueness in analytical results comparable to XRF. Black-Right-Pointing-Pointer The time needed and the complexity of LIBS analysis would not exceed the XRF ones.

  17. Potential radionuclide emissions from stacks on the Hanford site, Part 2: Dose assessment methodology using portable low-resolution gamma spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Barnett, J.M. [Westinghouse Hanford Company, Richland, WA (United States)

    1995-02-01

    In September 1992, the Westinghouse Hanford Company began developing an in situ measurement method to assess gamma radiation emanating from high-efficiency particulate air filters using portable low-resolution gamma spectroscopy. The purpose of the new method was to assess radioactive exhaust stack air emissions from empirical data rather than from theoretical models and to determine the potential unabated dose to an offsite theoretical maximally exposed individual. In accordance with Title 40, Code of Federal Regulations, Part 61, Subpart H, {open_quotes}National Emission Standards for Hazardous Air Pollutants{close_quotes}, stacks that have the potential to emit {ge} 1 {mu}Sv y{sup {minus}1} (0.1 mrem y{sup {minus}1}) to the maximally exposed individual are considered {open_quotes}major{close_quotes} and must meet the continuous monitoring requirements. After the method was tested and verified, the U.S. Environmental Protection Agency, Region 10, approved its use in June 1993. Of the 125 stacks operated by the Westinghouse Hanford Company, 22 were targeted for evaluation by this method, and 15 were assessed. (The method could not be applied at seven stacks because of excessive background radiation or because no gamma emitting particles appear in the emission stream.) The most significant result from this study was the redesignation of the T Plant main stack. The stack was assessed as being {open_quotes}minor{close_quotes}, and it now only requires periodic confirmatory measurements and meets federally imposed sampling requirements.

  18. Exploration of CdTe quantum dots as mesoscale pressure sensors via time-resolved shock-compression photoluminescent emission spectroscopy

    Science.gov (United States)

    Kang, Zhitao; Banishev, Alexandr A.; Lee, Gyuhyon; Scripka, David A.; Breidenich, Jennifer; Xiao, Pan; Christensen, James; Zhou, Min; Summers, Christopher J.; Dlott, Dana D.; Thadhani, Naresh N.

    2016-07-01

    The nanometer size of CdTe quantum dots (QDs) and their unique optical properties, including size-tunable narrow photoluminescent emission, broad absorption, fast photoluminescence decay, and negligible light scattering, are ideal features for spectrally tagging the shock response of localized regions in highly heterogeneous materials such as particulate media. In this work, the time-resolved laser-excited photoluminescence response of QDs to shock-compression was investigated to explore their utilization as mesoscale sensors for pressure measurements and in situ diagnostics during shock loading experiments. Laser-driven shock-compression experiments with steady-state shock pressures ranging from 2.0 to 13 GPa were performed on nanocomposite films of CdTe QDs dispersed in a soft polyvinyl alcohol polymer matrix and in a hard inorganic sodium silicate glass matrix. Time-resolved photoluminescent emission spectroscopy was used to correlate photoluminescence changes with the history of shock pressure and the dynamics of the matrix material surrounding the QDs. The results revealed pressure-induced blueshifts in emitted wavelength, decreases in photoluminescent emission intensity, reductions in peak width, and matrix-dependent response times. Data obtained for these QD response characteristics serve as indicators for their use as possible time-resolved diagnostics of the dynamic shock-compression response of matrix materials in which such QDs are embedded as in situ sensors.

  19. Spatio-spectral characteristics of ultra-broadband THz emission from two-colour photoexcited gas plasmas and their impact for nonlinear spectroscopy

    Science.gov (United States)

    Blank, V.; Thomson, M. D.; Roskos, H. G.

    2013-07-01

    We present a characterization of the combined spatial and spectral properties of the terahertz (THz) and mid-infrared emission from gas plasmas generated and driven by two-colour femtosecond optical pulses. For its use in nonlinear spectroscopy, the impact of the relatively complex spatial profile for both broadband (∼ 10 THz) and ultra-broadband (> 100 THz) emission needs to be considered, in particular for experiments based on z-scan techniques. Here we apply spatially resolved measurements based on both field autocorrelation and sum-frequency (up-conversion) detection. Based on these results, we present simulations of the ultra-broadband profile during its passage through a focal region. In addition to the inherent features of the emission profile due to the generation mechanism in the plasma filament, we also analyse the role of the semconductor (silicon) wafer typically placed after the plasma to discard the optical pump beams, whose photoexcitation also can play a role in the resultant THz profile.

  20. In situ diagnosis of pulsed UV laser surface ablation of tungsten carbide hardmetal by using laser-induced optical emission spectroscopy

    Science.gov (United States)

    Li, Tiejun; Lou, Qihong; Wei, Yunrong; Huang, Feng; Dong, Jingxing; Liu, Jingru

    2001-12-01

    Surface ablation of cobalt cemented tungsten carbide hardmetal with pulsed UV laser has been in situ diagnosed by using the technique of laser-induced optical emission spectroscopy. The dependence of emission intensity of cobalt lines on number of laser shots was investigated at laser fluence of 2.5 J/cm 2. As a comparison, the reliance of emission intensity of cobalt lines as a function of laser pulse number by using pure cobalt as ablation sample was also studied at the same laser condition. It was found that for surface ablation of tungsten carbide hardmetal at laser fluence of 2.5 J/cm 2, the intensities of cobalt lines fell off dramatically in the first 300 consecutive laser shots and then slowed down to a low stable level with even more shots. For surface ablation of pure cobalt at the same laser condition, the intensities of cobalt lines remained constant more or less even after 500 laser shots and then reduced very slowly with even more shots. It was concluded that selective evaporation of cobalt at this laser fluence should be responsible for the dramatic fall-off of cobalt lines with laser shots accumulation for surface ablation of tungsten carbide hardmetal. In contrast, for surface ablation of pure cobalt, the slow reduction of cobalt lines with pulse number accumulation should be due to the formation of laser-induced crater effect.

  1. Photolysis of n-butyl nitrite and isoamyl nitrite at 355 nm: A time-resolved Fourier transform infrared emission spectroscopy and ab initio study

    CERN Document Server

    Ji, Min; Zhang, Qun; Chen, Yang

    2009-01-01

    We report on the photodissociation dynamics study of n-butyl nitrite (n-C_4H_9ONO) and isoamyl nitrite ((CH_3)_2C_3H_5ONO) by means of time-resolved Fourier transform infrared (TR-FTIR) emission spectroscopy. The obtained TR-FTIR emission spectra of the nascent NO fragments produced in the 355-nm laser photolysis of the two alkyl nitrite species showed an almost identical rotational temperature and vibrational distributions of NO. In addition, a close resemblance between the two species was also found in the measured temporal profiles of the IR emission of NO and the recorded UV absorption spectra. The experimental results are consistent with our ab initio calculations using the time-dependent density functional theory at the B3LYP/6-311G(d,p) level, which indicate that the substitution of one of the two {gamma}-H atoms in n-C_4H_9ONO with a methyl group to form (CH_3)_2C_3H_5ONO has only a minor effect on the photodissociation dynamics of the two molecules.

  2. Interactions of protons with furan molecules studied by collision-induced emission spectroscopy at the incident energy range of 50-1000 eV

    Science.gov (United States)

    Wasowicz, Tomasz J.; Pranszke, Boguslaw

    2016-08-01

    Investigations of the ion-molecule reactions provide insight into many fields ranging from the stellar wind interaction with interstellar media, up to medicine and industrial applications. Besides the applications, the understanding of these processes is itself a problem of fundamental importance. Thus, interactions of protons with the gas-phase furan molecules have been investigated for the first time in the energy range of 50-1000 eV exploiting collision-induced emission spectroscopy. Recorded spectra reveal emission of the atomic H β to H θ lines of the hydrogen Balmer series and the molecular bands of vibrationally and rotationally excited diatomic CH fragments created in the A2 Δ and B2Σ- electronic states. The measurements of the emission yields of the excited fragments by recording their intensities at different projectile energies have been performed. The highest yields have been observed for production of hydrogen atoms which intensities rapidly decreased with increasing principal quantum number n . From the H ( n = 4-7) intensity ratios depopulation factors of hydrogen excited states have been determined at each impact energy and possible collisional mechanisms leading to enhanced production of the hydrogen atoms have been suggested. We compare and discuss our results with improved data set of proton collisions with tetrahydrofuran (THF) molecules, the hydrogenated derivatives of furan.

  3. Time-resolved measurement of atomic emission enhancement by fs-ns dual-pulsed laser-induced breakdown spectroscopy

    Institute of Scientific and Technical Information of China (English)

    Yan Li-Xin; Zhang Yong-Sheng; Zheng Guo-Xin; Liu Jing-Ru; Cheng Jian-Ping; Lü Min

    2006-01-01

    Time-resolved measurement of atomic emission enhancement is performed by using a 500-fs KrF laser pulse incident upon a high density supersonic O2 gas jet, synchronized with an orthogonal ns frequency-doubled Nd:YAG laser pulse. The ultra-short pulse serves as an igniter of the gas jet, and the subsequent ns-laser pulse significantly enhances the atomic emission. Analysis shows that the contributions to the enhancement effect are made mainly by the bremsstrahlung radiation and cascade ionization.

  4. Phosphorus Speciation of Sequential Extracts of Organic Amendments using NMR Spectroscopy

    Science.gov (United States)

    Akinremi, O.

    2009-04-01

    O.O. 1Akinremi Babasola Ajiboye and Donald N. Flaten 1Department of Soil Science, University of Manitoba, Winnipeg, R3T 2NT, Canada We carried out this study in order to determine the forms of phosphorus in various organic amendments using state-of-the art spectroscopic technique. Anaerobically digested biosolids (BIO), hog (HOG), dairy (DAIRY), beef (BEEF) and poultry (POULTRY) manures were subjected to sequential extraction. The extracts were analyzed by solution 31P nuclear magnetic resonance (NMR) spectroscopy. Most of the total P analysed by inductively coupled plasma-optical emission spectroscopy (ICP-OES) in the sequential extracts of organic amendments were orthophosphate, except POULTRY, which was dominated by organic P. The labile P fraction in all the organic amendments, excluding POULTRY, was mainly orthophosphate P from readily soluble calcium and some aluminum phosphates. In the poultry litter, however, Ca phytate was the main P species controlling P solubility. Such knowledge of the differences in the chemical forms of phosphorus in organic amendments are essential for proper management of these amendments for agro-environmental purposes Key words: organic amendments, solution NMR, sequential fractionation, labile phosphorus

  5. Prediction of methane emission from lactating dairy cows using milk fatty acids and mid-infrared spectroscopy

    NARCIS (Netherlands)

    Derksen-van Gastelen, Sanne; Dijkstra, Jan

    2016-01-01

    Enteric methane (CH4) production is among the main targets of greenhouse gas mitigation practices for the dairy industry. A simple, robust and inexpensive measurement technique applicable on a large scale to estimate CH4 emission from dairy cattle would therefore be valuable

  6. Near-Infrared Spectroscopy of Faint Discrete X-ray Point Sources Constituting the Galactic Ridge X-ray Emission

    CERN Document Server

    Morihana, Kumiko; Dubath, Pierre; Yoshida, Tessei; Suzuki, Kensuke; Ebisawa, Ken

    2016-01-01

    The Galactic Ridge X-ray Emission (GRXE) is apparently extended X-ray emission along the Galactic Plane. The X-ray spectrum is characterized by hard continuum with a strong Fe K emission feature in the 6-7 keV band. A substantial fraction (~80%) of the GRXE in the Fe band was resolved into point sources by deep Chandra imaging observations, thus GRXE is mostly composed of dim Galactic X-ray point sources at least in this energy band. To investigate the populations of these dim X-ray point sources, we carried out Near-Infrared (NIR) follow-up spectroscopic observations in two deep Chandra fields located in the Galactic plane at (l,b)=(0.1{\\arcdeg}, -1.4{\\arcdeg}) and (28.5{\\arcdeg}, 0.0{\\arcdeg}) using NTT/SofI and Subaru/MOIRCS. We obtained well-exposed NIR spectra from 65 objects and found that there are three main classes of Galactic sources based on the X-ray color and NIR spectral features: those having (A) hard X-ray spectra and NIR emission features such as HI(Br{\\gamma}), HeI, and HeII (2 objects), (B)...

  7. Predicting methane emissions of lactating Danish Holstein cows using Fourier transform mid-infrared spectroscopy of milk

    NARCIS (Netherlands)

    Shetty, N.P.; Difford, G.; Lassen, J.; Løvendahl, P.; Buitenhuis, A.J.

    2017-01-01

    Enteric methane (CH4), a potent greenhouse gas, is among the main targets of mitigation practices for the dairy industry. A measurement technique that is rapid, inexpensive, easy to use, and applicable at the population level is desired to estimate CH4 emission from dairy cows. In the present study,

  8. Advanced techniques for actinide spectroscopy (ATAS 2012). Abstract book

    Energy Technology Data Exchange (ETDEWEB)

    Foerstendorf, Harald; Mueller, Katharina; Steudtner, Robin (eds.)

    2012-07-01

    The abstract book of the International workshop on advanced techniques for actinide spectroscopy (ATAS 2012) include contributions concerning the following issues: environmental applications, NMR spectroscopy, vibrational spectroscopy, X-ray spectroscopy and theory, technical application: separation processes, emission spectroscopy.

  9. Observation of Atomic Emission Enhancement by fs-ns Dual-Pulse Laser-Induced Breakdown Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    YAN Li-Xin; ZHANG Yong-Sheng; ZHANG Li-Rong; LIU Jing-Ru; CHENG Jian-Ping; L(U) Min

    2006-01-01

    An experiment of a 500-fs KrF laser pulse incident upon a high density supersonic O2 gas jet synchronously with an ns frequency-doubled Nd:YAG laser pulse is performed in orthogonal configuration.Significant atomic emission enhancement of over forty-fold is observed with an optical multi-channel analyser.The enhancement effect is probably attributed to the different ionization mechanisms between fs and ns laser pulses.

  10. Electron density in amplitude modulated microwave atmospheric plasma jet as determined from microwave interferometry and emission spectroscopy

    Science.gov (United States)

    Faltýnek, J.; Hnilica, J.; Kudrle, V.

    2017-01-01

    Time resolved electron density in an atmospheric pressure amplitude modulated microwave plasma jet is determined using the microwave interferometry method, refined by numerical modelling of the propagation of non-planar electromagnetic waves in the vicinity of a small diameter, dense collisional plasma filament. The results are compared to those from the Stark broadening of the {{\\text{H}}β} emission line. Both techniques show, both qualitatively and quantitatively, a similar temporal evolution of electron density during one modulation period.

  11. Light emission of a polyfluorene derivative containing complexed europium ions.

    Science.gov (United States)

    Turchetti, Denis Augusto; Nolasco, Mariela Martins; Szczerbowski, Daiane; Carlos, Luís Dias; Akcelrud, Leni Campos

    2015-10-21

    The photophysical properties of a new alternating copolymer containing fluorene, terpyridine, and complexed sites with trivalent europium (Eu(3+)) ions (LaPPS66Eu) were investigated, using the non-complexed backbone (LaPPS66) and a low molecular weight compound of similar chemical structure of the ligand/Eu(3+) site (LaPPS66M) as a model compound. The analogous gadolinium complex (LaPPS66Gd) was also synthesized to determine the triplet state of the complex. (1)H and (13)C nuclear magnetic resonance (NMR) analysis, Fourier transform infrared (FT-IR) spectroscopy, inductively coupled plasma optical emission spectroscopy (ICP-OES), elemental analyses, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) characterized the chemical structure and thermal properties of the synthesized materials. A level of Eu(3+) insertion of 37% (molar basis) in the polymer backbone was achieved. The photoluminescence studies were performed in the solid state showing the occurrence of polymer-to-Eu(3+) energy transfer brought about by the spectral overlap between the absorption spectra of the Eu(3+) complex and the emission of the polymer backbone. A detailed theoretical photoluminescence study performed using time-dependent DFT (TD-DFT) calculations and the recently developed LUMPAC luminescence package is also presented. The high accuracy of the theoretical calculations was achieved on comparison with the experimental values. Aiming at a deeper level of understanding of the photoluminescence process, the ligand-to-Eu(3+) intramolecular energy transfer and back-transfer rates were predicted. The complexed materials showed a dominant pathway involving the energy transfer between the triplet of the dbm (dibenzoylmethane) ligand and the (5)D1 and (5)D0 Eu(3+) levels.

  12. Excited State Chemistry in the Free Stream of the NASA IHF Arc Jet Facility Observed by Emission Spectroscopy

    Science.gov (United States)

    Winter, Michael W.; Prabhu, Dinesh K.

    2011-01-01

    Spectroscopic measurements of non-equilibrium emission were made in the free stream of the 60 megawatts Interaction Heating Facility at NASA Ames Research Center. In the visible near infrared wavelength region, the most prominent emission was from molecular N2, and in the ultra violet region, the spectra were dominated by emission from molecular NO. The only atomic lines observed were those of copper (an erosion product of the electrodes). The bands of the 1st Positive system of N2 (if B is true then A is true) differed significantly from spectra computed spectra assuming only thermal excitation, suggesting overpopulation of the high vibrational states of the B state of N2. Populations of these high vibrational levels (peaking at v (sub upper) equals 13) of the N2 B state were determined by scaling simulated spectra; calculations were performed for each upper vibrational state separately. The experimental-theoretical procedure was repeated for several radial positions away from the nozzle axis to obtain spatial distributions of the upper state populations; rotational symmetry of the flow was assumed in simulations. The overpopulation of the high vibrational levels has been interpreted as the effect of inverse pre-dissociation of neutral atoms in the N2 A state, which populates the N2 B state through a level crossing process at v (sub upper) is greater than 10.

  13. Influence of COsub>2sub> pressure on the emission spectra and plasma parameters in underwater laser-induced breakdown spectroscopy.

    Science.gov (United States)

    Goueguel, Christian L; McIntyre, Dustin L; Jain, Jinesh C

    2016-12-01

    Optical emission spectroscopic studies have been carried out to investigate the pressure effect of COsub>2sub> on laser-produced underwater plasma. The plasma was generated by focusing 1064 nm, 6 ns pulses from a Nd:YAG laser in a COsub>2sub>-bearing solution. The temporal evolution of the continuum emission, Sr and Ba lines, and plasma electron density and temperature was characterized under COsub>2sub> pressure ranging from 10 to 300 bars. The electron density measurements were made using the Stark broadening of the 455.40 nm Ba II line, while the temperature measurements have been performed by the Saha-Boltzmann method using the Sr I-II lines at 460.73 and 407.77 nm, respectively. It was found that COsub>2sub> pressure has little effect on the emission line intensity and signal-to-background ratio. The electron density and the temperature are found to be independent of the COsub>2sub> pressure at early times. When time becomes longer, the electron density exhibits an appreciable rise as the COsub>2sub> pressure increases, while the temperature is found to be unchanged.

  14. Observation of Coriolis Coupling between nu(2) + 4nu(4) and 7nu(4) in Acetylene &Xtilde;(1)Sigma(+)(g) by Stimulated Emission Pumping Spectroscopy.

    Science.gov (United States)

    Moss; Duan; Jacobson; O'Brien; Field

    2000-02-01

    Stimulated emission pumping (SEP) spectroscopy has been used to examine a low energy region (E(vib) approximately 4400 cm(-1)) of &Xtilde;(1)Sigma(+)(g) acetylene at higher resolution than was possible in previous dispersed fluorescence studies. The expected bright state, nu(2) + 4nu(4), is observed to be coupled to the nearly degenerate 7nu(4) state by a Coriolis mechanism. A least-squares analysis yields values for zero-order vibrational energies, rotational constants, and a Coriolis-coupling coefficient that are all consistent with expectations. Calculated relative intensities of SEP transitions, accounting for interference due to axis-switching effects, are also consistent with observations. Implications of the observed Coriolis resonance with regard to global acetylene vibrational dynamics are also discussed. Copyright 2000 Academic Press.

  15. Current opportunities and challenges of magnetic resonance spectroscopy, positron emission tomography, and mass spectrometry imaging for mapping cancer metabolism in vivo.

    Science.gov (United States)

    Lin, Gigin; Chung, Yuen-Li

    2014-01-01

    Cancer is known to have unique metabolic features such as Warburg effect. Current cancer therapy has moved forward from cytotoxic treatment to personalized, targeted therapies, with some that could lead to specific metabolic changes, potentially monitored by imaging methods. In this paper we addressed the important aspects to study cancer metabolism by using image techniques, focusing on opportunities and challenges of magnetic resonance spectroscopy (MRS), dynamic nuclear polarization (DNP)-MRS, positron emission tomography (PET), and mass spectrometry imaging (MSI) for mapping cancer metabolism. Finally, we highlighted the future possibilities of an integrated in vivo PET/MR imaging systems, together with an in situ MSI tissue analytical platform, may become the ultimate technologies for unraveling and understanding the molecular complexities in some aspects of cancer metabolism. Such comprehensive imaging investigations might provide information on pharmacometabolomics, biomarker discovery, and disease diagnosis, prognosis, and treatment response monitoring for clinical medicine.

  16. Analysis of the absorption spectra of gas emission of patients with lung cancer and chronic obstructive pulmonary disease by laser optoacoustic spectroscopy

    Science.gov (United States)

    Bukreeva, Ekaterina B.; Bulanova, Anna A.; Kistenev, Yurii V.; Kuzmin, Dmitry A.; Tuzikov, Sergei A.; Yumov, Evgenii L.

    2013-02-01

    It is important to identify patients with chronic obstructive pulmonary disease (COPD) and lung cancer in the early stages of the disease. The method of laser opto-acoustic gas analysis, in this case, can act as a promising tool for diagnostics. The material for this study were the gas emission samples collected from patients and healthy volunteers - samples of exhaled air, swabs from teeth and cheeks. A set of material was formed three groups: healthy volunteers, patients with COPD, lung cancer patients. The resulting samples were analyzed by means of laser opto-acoustic gas analyzers: with intracavity location detector (ILPA-1), with extracavity location detector (LGA-2). Presentation of the results in an easy to visual form was performed using the method of elastic maps, based on the principal component analysis. The results of analysis show potentialities of usage of laser optoacoustic spectroscopy application to assess the status of patients with chronic obstructive pulmonary disease and lung cancer.

  17. Application of inductively coupled plasma atomic emission spectroscopy analysis with a polychromator/monochromator combination the byproducts of coal-fired power stations

    Science.gov (United States)

    Weers, C. A.

    The by-products of coal-fired power plants may be hazardous for the environment. Good analysis methods are therefore required in order to establish either a possible usage of the by-products or their possible storage. Preliminary experiments performed with inductively coupled plasma atomic emission spectroscopy have proven very successful. Moreover, the method is cost-effective. A short description is given of the optimized system for routine analysis. The system consists of a 2- and a 15-channel polychromator in combination with a monochromator. The opportunities is provides are also described. Use of the monochromator to analyze coal and run-off water from the flue-gases desulphurization, and of the polychromators to analyze coal fly-ash is described separately.

  18. Delocalization and occupancy effects of 5f orbitals in plutonium intermetallics using L3-edge resonant X-ray emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Booth, C. H.; Medling, S. A.; Jiang, Yu; Bauer, E. D.; Tobash, P. H.; Mitchell, J. N.; Veirs, D. K.; Wall, M. A.; Allen, P. G.; Kas, J. J.; Sokaras, D.; Nordlund, D.; Weng, T. -C.

    2014-06-24

    Although actinide (An) L3 -edge X-ray absorption near-edge structure (XANES) spectroscopy has been very effective in determining An oxidation states in insulating, ionically bonded materials, such as in certain coordination compounds and mineral systems, the technique fails in systems featuring more delocalized 5f orbitals, especially in metals. Recently, actinide L3-edge resonant X-ray emission spec- troscopy (RXES) has been shown to be an effective alternative. This technique is further demonstrated here using a parameterized partial unoccupied density of states method to quantify both occupancy and delocalization of the 5f orbital in ?-Pu, ?-Pu, PuCoGa5 , PuCoIn5 , and PuSb2. These new results, supported by FEFF calculations, highlight the effects of strong correlations on RXES spectra and the technique?s ability to differentiate between f-orbital occupation and delocalization.

  19. Energy-dispersive x-ray fluorescence spectroscopy and inductively coupled plasma emission spectrometry evaluated for multielement analysis in complex biological matrices.

    Science.gov (United States)

    Irons, R D; Schenk, E A; Giauque, R D

    1976-12-01

    Energy-dispersive x-ray spectroscopy and inductively coupled plasma emission spectrometry were evaluated as methods for routine multielement analysis of biological material. Standard samples included Standard Reference Materials (National Bureau of Standards), compounded mixtures, and supplements that provided a wide range of elemental concentrations for analysis. Elements included in this study were Zn, Pb, Ni, Mn, Fe, Mg, Cu, Ca, As, Se, Br, Rb, and Sr. Standards were analyzed as unknowns by participating laboratories. The two methods were evaluated for sensitivity, precision, and accuracy, and the results compared to those obtained for atomic absorption spectrometric analysis of identical standard unknowns. Both methods compared favorably and both were determined to be highly reliable for such an application. Advantages and disadvantages of each method are compared and discussed.

  20. Study of effect of H2 addition on the production of fluorocarbon radicals in H2/C4F8 inductively coupled plasma via optical emission spectroscopy actinometry

    Institute of Scientific and Technical Information of China (English)

    Huang Song; Xin Yu; Ning Zhao-Yuan

    2005-01-01

    C4F8 plasma with the addition of H2 is generated by the inductively coupled plasma (ICP) method. The relative densities of CF, CF2, H and F radicals are determined by actinometric optical emission spectroscopy (AOES) as a function of the gas flow rate ratio R=H2/(H2+C4F8) at a pressure of 0.8 Pa and an input r.f. power of 400W, while that of HF is measured by quadrupole mass spectrometry (QMS). The results show that plasma activity increases firstly and then decreases with increasing R. As the gas flow rate ratio R changes from 0 to 0.625, relative densities of both CF and CF2 decrease, and the relative [CF] has a similar tendency as the calculated [CF], indicating that CF radicals are generated mainly by the electron impact dissociation of CF2 radicals. Production of HF is also discussed.

  1. Gas phase optical emission spectroscopy during remote plasma chemical vapour deposition of GaN and relation to the growth dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Corr, Cormac; Boswell, Rod [Space Plasma, Power and Propulsion Group, Plasma Research Laboratory, Research School of Physics and Engineering, Australian National University, Canberra 0200 (Australia); Carman, Robert [Physics Department, Macquarie University, North Ryde, Sydney, NSW 2109 (Australia)

    2011-02-02

    A remote plasma chemical vapour deposition (RPCVD) system for the growth of gallium nitride (GaN) thin films is investigated using optical emission spectroscopy (OES). The intensities of the various excited species in pure nitrogen as well as nitrogen/hydrogen plasmas are correlated with GaN film growth characteristics. We show a correlation between the plasma source spectrum, the downstream spectrum where trimethylgallium is introduced and the GaN film quality. In particular, we investigate the addition of hydrogen, which greatly affects the gas phase species and the GaN film characteristics. OES is demonstrated to be a valuable monitoring tool in a RPCVD system for optimization of GaN growth.

  2. Electron correlation energy of La sub x Sr sub 1 sub - sub x TiO sub 3 by high-resolution soft-X-ray emission spectroscopy

    CERN Document Server

    Higuchi, T; Tsukamoto, T; Harada, Y; Taguchi, Y; Tokura, Y; Shin, S

    2003-01-01

    The electronic structure of La sub x Sr sub 1 sub - sub x TiO sub 3 (x<=0.10) has been investigated by high-resolution soft-X-ray emission spectroscopy (SXES) spectra in the Ti 2p energy region. At the t sub 2 sub g -resonance SXES spectra, the d-d transition whose Raman shift is about 2.2 eV corresponds to the magnitude of the half intra-atomic Coulomb energy (U sub d sub d /2). The magnitude does not change in x<=0.10. This fact is consistent with the results obtained from the effective mass and the electronic specific heat.

  3. Highly polarized emission in spin resolved photoelectron spectroscopy of alpha-Fe(001)/GaAs(001)

    Energy Technology Data Exchange (ETDEWEB)

    Tobin, James; Yu, Sung Woo; Morton, Simon; Waddill, George; Thompson, Jamie; Neal, James; Spangenberg, Matthais; Shen, T.H.

    2009-05-19

    Highly spin-polarized sources of electrons, Integrated into device design, remain of great interest to the spintronic and magneto-electronic device community Here, the growth of Fe upon GaAs(001) has been studied with photoelectron spectroscopy (PES), including Spin Resolved PES. Despite evidence of atomic level disorder such as intermixing, an over-layer with the spectroscopic signature of alpha-Fe(001), with a bcc real space ordering, Is obtained The results will be discussed in light of the possibility of using such films as a spin-polarized source in device applications.

  4. Spectral and spatial resolution of the 12.8 micron Ne 2 emission from the galactic center. [astronomical spectroscopy/emission spectra, radio sources (astronomy)

    Science.gov (United States)

    Wollman, E. R.; Geballe, T. R.; Lacy, J. H.; Townes, C. H.; Rank, D. M.

    1975-01-01

    High-resolution spectra of the Ne II 12.8 micron fine-structure line in emission from the galactic center cloud Sgr A West show a line-center LSR radial velocity of + 75 + or - 20 km/sec. and a velocity dispersion of about 200 km/sec. The line has been observed with spectral resolution as high as 0.10/cm and spatial resolution as high as 8 sec. This appears to provide a direct measurement of conditions in the 45 sec. ionized region at the galactic center. The radial velocity and dispersion are more-or-less independent of position and indicate that events as recent as the last 4 million years have given the ionized gas a systematic motion with respect to the massive stellar component of material at the galactic center. An upper limit for the mass approximately equal to four million times the solar mass was obtained from the velocity distribution, with the mass located within 0.8 parsecs of the galactic center.

  5. Quantifying aflatoxins in peanuts using fluorescence spectroscopy coupled with multi-way methods: Resurrecting second-order advantage in excitation-emission matrices with rank overlap problem.

    Science.gov (United States)

    Sajjadi, S Maryam; Abdollahi, Hamid; Rahmanian, Reza; Bagheri, Leila

    2016-03-05

    A rapid, simple and inexpensive method using fluorescence spectroscopy coupled with multi-way methods for the determination of aflatoxins B1 and B2 in peanuts has been developed. In this method, aflatoxins are extracted with a mixture of water and methanol (90:10), and then monitored by fluorescence spectroscopy producing EEMs. Although the combination of EEMs and multi-way methods is commonly used to determine analytes in complex chemical systems with unknown interference(s), rank overlap problem in excitation and emission profiles may restrain the application of this strategy. If there is rank overlap in one mode, there are several three-way algorithms such as PARAFAC under some constraints that can resolve this kind of data successfully. However, the analysis of EEM data is impossible when some species have rank overlap in both modes because the information of the data matrix is equivalent to a zero-order data for that species, which is the case in our study. Aflatoxins B1 and B2 have the same shape of spectral profiles in both excitation and emission modes and we propose creating a third order data for each sample using solvent as a new additional selectivity mode. This third order data, in turn, converted to the second order data by augmentation, a fact which resurrects the second order advantage in original EEMs. The three-way data is constructed by stacking augmented data in the third way, and then analyzed by two powerful second order calibration methods (BLLS-RBL and PARAFAC) to quantify the analytes in four kinds of peanut samples. The results of both methods are in good agreement and reasonable recoveries are obtained.

  6. Quantifying aflatoxins in peanuts using fluorescence spectroscopy coupled with multi-way methods: Resurrecting second-order advantage in excitation-emission matrices with rank overlap problem

    Science.gov (United States)

    Sajjadi, S. Maryam; Abdollahi, Hamid; Rahmanian, Reza; Bagheri, Leila

    2016-03-01

    A rapid, simple and inexpensive method using fluorescence spectroscopy coupled with multi-way methods for the determination of aflatoxins B1 and B2 in peanuts has been developed. In this method, aflatoxins are extracted with a mixture of water and methanol (90:10), and then monitored by fluorescence spectroscopy producing EEMs. Although the combination of EEMs and multi-way methods is commonly used to determine analytes in complex chemical systems with unknown interference(s), rank overlap problem in excitation and emission profiles may restrain the application of this strategy. If there is rank overlap in one mode, there are several three-way algorithms such as PARAFAC under some constraints that can resolve this kind of data successfully. However, the analysis of EEM data is impossible when some species have rank overlap in both modes because the information of the data matrix is equivalent to a zero-order data for that species, which is the case in our study. Aflatoxins B1 and B2 have the same shape of spectral profiles in both excitation and emission modes and we propose creating a third order data for each sample using solvent as a new additional selectivity mode. This third order data, in turn, converted to the second order data by augmentation, a fact which resurrects the second order advantage in original EEMs. The three-way data is constructed by stacking augmented data in the third way, and then analyzed by two powerful second order calibration methods (BLLS-RBL and PARAFAC) to quantify the analytes in four kinds of peanut samples. The results of both methods are in good agreement and reasonable recoveries are obtained.

  7. Measurement of the hot spot electron temperature in NIF ICF implosions using Krypton x-ray emission spectroscopy

    Science.gov (United States)

    Ma, T.; Chen, H.; Patel, P. K.; Schneider, M.; Barrios, M.; Berzak Hopkins, L.; Casey, D.; Chung, H.-K.; Hammel, B.; Jarrott, C.; Nora, R.; Pak, A.; Scott, H.; Spears, B.; Weber, C.

    2015-11-01

    The inference of ion temperature from neutron spectral measurements in indirect-drive ICF implosions is known to be sensitive to non-thermal velocity distributions in the fuel. The electron temperature (Te) inferred from dopant line ratios should not be sensitive to these bulk motions and hence may be a better measure of the thermal temperature of the hot spot. Here we describe a series of experiments to be conducted on the NIF where a small concentration of a mid-Z dopant (Krypton) is added to the fuel gas. The x-ray spectra is measured and the electron temperature is inferred from Kr line ratios. We also quantify the level of radiative cooling in the hot spot due to this mid-Z dopant. These experiments represent the first direct measurement of hot spot Te using spectroscopy, and we will describe the considerations for applying x-ray spectroscopy in such dense and non-uniform hot spots. This work performed under the auspices of U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344.

  8. X-ray absorption and emission spectroscopy of Cr(III) (hydr)oxides: analysis of the K-pre-edge region.

    Science.gov (United States)

    Frommer, Jakob; Nachtegaal, Maarten; Czekaj, Izabela; Weng, Tsu-Chien; Kretzschmar, Ruben

    2009-11-05

    Pre-edge spectral features below the main X-ray absorption K-edge of transition metals show a pronounced chemical sensitivity and are promising sources of structural information. Nevertheless, the use of pre-edge analysis in applied research is limited because of the lack of definite theoretical peak-assignments. The aim of this study was to determine the factors affecting the chromium K-pre-edge features in trivalent chromium-bearing oxides and oxyhydroxides. The selected phases varied in the degree of octahedral polymerization and the degree of iron-for-chromium substitution in the crystal structure. We investigated the pre-edge fine structure by means of high-energy-resolution fluorescence detected X-ray absorption spectroscopy and by 1s2p resonant X-ray emission spectroscopy. Multiplet theory and full multiple-scattering calculations were used to analyze the experimental data. We show that the chromium K-pre-edge contains localized and nonlocalized transitions. Contributions arising from nonlocalized metal-metal transitions are sensitive to the nearest metal type and to the linkage mode between neighboring metal octahedra. Analyzing these transitions opens up new opportunities for investigating the local coordination environment of chromium in poorly ordered solids of environmental relevance.

  9. Emission and absorption spectroscopy study of Ar excited states in 13.56 MHz argon plasma operating at sub-atmospheric to atmospheric pressure

    Energy Technology Data Exchange (ETDEWEB)

    Li, L. [Department of Applied Physics, Research Unit Plasma Technology, Ghent University, Jozef Plateaustraat 22, Ghent B-9000 (Belgium); Nikiforov, A., E-mail: anton.nikiforov@ugent.be [Department of Applied Physics, Research Unit Plasma Technology, Ghent University, Jozef Plateaustraat 22, Ghent B-9000 (Belgium); Institute of Solution Chemistry of the Russian Academy of Science, Academicheskaya St., 1, Ivanovo, 153045 (Russian Federation); Britun, N. [Chimie des Interactions Plasma-Surface (ChIPS), CIRMAP, Universite de Mons, 23 Place du Parc, B-7000 Mons (Belgium); Snyders, R. [Chimie des Interactions Plasma-Surface (ChIPS), CIRMAP, Universite de Mons, 23 Place du Parc, B-7000 Mons (Belgium); Materia Nova Research Centre, Parc Initialis, B-7000 Mons (Belgium); Leys, C. [Department of Applied Physics, Research Unit Plasma Technology, Ghent University, Jozef Plateaustraat 22, Ghent B-9000 (Belgium)

    2015-05-01

    The densities of metastable and resonant states of Ar atoms are measured in high pressure Ar radio frequency discharge. Resonant absorption spectroscopy for the case of a low pressure spectral lamp and high-pressure plasma absorption lines is implemented for this purpose. The necessary generalizations for the high-pressure resonant absorption method are given. Absolute density of Ar 1s levels obtained at different RF input power and operating pressures are of the order of 10{sup 11} cm{sup −3}, which is in a good agreement with those reported in the literature. The population distribution on the Ar 2p (excited) levels, obtained from the optical emission spectroscopy, reveals strong deviation from thermal equilibrium for these levels in the high-pressure case. The generation of the Ar excited states in the studied discharges is compared to the previously reported results. - Highlights: • Strong non-equilibrium distribution of Ar 2p levels is observed. • The absolute number density of non-radiative Ar 1s states is determined by the easier and low cost spectral-lamp absorption method. • The modified absorption theory of Mitchell and Zemanski was used to obtain the absolute number density of Ar 1s states at high pressure. • The developed RF source with 5 cm long gap can be a possible alternative to micro-plasma working in Ar at atmospheric pressure.

  10. Measurement of Electron Density Using the Multipole Resonance Probe, Langmuir Probe and Optical Emission Spectroscopy in Low Pressure Plasmas with Different Electron Energy Distribution Functions

    Science.gov (United States)

    Oberberg, Moritz; Bibinov, Nikita; Ries, Stefan; Awakowicz, Peter; Institute of Electrical Engineering; Plasma Technology Team

    2016-09-01

    In recently publication, the young diagnostic tool Multipole Resonance Probe (MRP) for electron density measurements was introduced. It is based on active plasma resonance spectroscopy (APRS). The probe was simulated und evaluated for different devices. The geometrical and electrical symmetry simplifies the APRS model, so that the electron density can be easily calculated from the measured resonance. In this work, low pressure nitrogen mixture plasmas with different electron energy distribution functions (EEDF) are investigated. The results of the MRP measurement are compared with measurements of a Langmuir Probe (LP) and Optical Emission Spectroscopy (OES). Probes and OES measure in different regimes of kinetic electron energy. Both probes measure electrons with low kinetic energy (<10 eV), whereas the OES is influenced by electrons with high kinetic energy which are needed for transitions of molecule bands. By the determination of the absolute intensity of N2(C-B) and N2+(B-X)electron temperature and density can be calculated. In a non-maxwellian plasma, all plasma diagnostics need to be combined.

  11. Investigation on Methane Decomposition and the Formation of C2 Hydrocarbons in DC Discharge Plasma byEmission Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    贺建勋; 韩媛媛; 高爱华; 周引穗; 陆治国

    2004-01-01

    The IR emission spectra of methane were measured under DC glow discharge conditions. The distinct difference in time between methane decomposition and C2 hydrocarbons formation was specially pointed out. C2 hydrocarbons formed at the end of methane decomposition. The optimum condition for C2 hydrocarbon formation was studied and the optimum combination between electric current density and methane input quantity was suggested. The appropriate reaction conditions for methane decomposition and C2 hydrocarbons formation are different, so high yield of C2 hydrocarbons will be probably obtained when different conditions are taken.

  12. Temperature measurement of plasma-assisted flames: comparison between optical emission spectroscopy and 2-color laser induced fluorescence techniques

    KAUST Repository

    Lacoste, Deanna A.

    2015-03-30

    Accurate thermometry of highly reactive environments, such as plasma-assisted combustion, is challenging. With the help of conical laminar premixed methane-air flames, this study compares two thermometry techniques for the temperature determination in a combustion front enhanced by nanosecond repetitively pulsed (NRP) plasma discharges. Based on emission spectroscopic analysis, the results show that the rotational temperature of CH(A) gives a reasonable estimate for the adiabatic flame temperature, only for lean and stoichiometric conditions. The rotational temperature of N2(C) is found to significantly underestimate the flame temperature. The 2-color OH-PLIF technique gives correct values of the flame temperature.

  13. Emission Characteristics of Laser-Induced Plasma Using Collinear Long and Short Dual-Pulse Laser-Induced Breakdown Spectroscopy (LIBS).

    Science.gov (United States)

    Wang, Zhenzhen; Deguchi, Yoshihiro; Liu, Renwei; Ikutomo, Akihiro; Zhang, Zhenzhen; Chong, Daotong; Yan, Junjie; Liu, Jiping; Shiou, Fang-Jung

    2017-09-01

    Collinear long and short dual-pulse laser-induced breakdown spectroscopy (DP-LIBS) was employed to clarify the emission characteristics from laser-induced plasma. The plasma was sustained and became stable by the long pulse-width laser with the pulse width of 60 μs 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.

  14. Direct determination of the nutrient profile in plant materials by femtosecond laser-induced breakdown spectroscopy.

    Science.gov (United States)

    de Carvalho, Gabriel Gustinelli Arantes; Moros, Javier; Santos, Dário; Krug, Francisco José; Laserna, J Javier

    2015-05-30

    Femtosecond laser-induced breakdown spectroscopy (fs-LIBS) has been used for the first time for quantitative determination of nutrients in plant materials from different crops. A highly heterogeneous population of 31 samples, previously analyzed by inductively coupled plasma optical emission spectroscopy, covering a wide range of matrices was interrogated. To tackle the analysis, laser-induced plasmas under argon atmosphere of pellets prepared from sieved cryogenically ground leaves were studied. Predictive functions based on univariate and multivariate modeling of optical emissions associated to macro- (Ca, Mg, and P) and micronutrients (Cu, Fe, Mn and Zn) were designed. Hierarchical cluster analysis was performed to select representative calibration (n(cal)=17) and validation (n(val)=14) datasets. The predictive performance of calibration functions over fs-LIBS data was compared with that attained on spectral information from nanosecond LIBS (ns-LIBS) operating at different wavelengths (1064 nm, 532 nm, and 266 nm). Findings established higher accuracy and less uncertainty on mass fractions quantification from fs-LIBS, whatever the modeling approach. Quality coefficients below 20% for the accuracy error on mass fractions' prediction in unknown samples, and residual predictive deviations in general above 5, were obtained. In contrast, only multivariate modeling satisfactorily handled the non-linear variations of emissions in ns-LIBS, leading to 2-fold decrease in the root mean square error of prediction (RMSEP) of Ca, Mg, P, Cu, Fe, Mn and Zn in comparison with the univariate approach. But still, an averaged quality coefficient about 35% and residual predictive deviations below 3 were found. Similar predictive capabilities were observed when changing the laser wavelength. Although predicted values by ns-LIBS multivariate modeling exhibit better agreement with reference mass fractions as compared to univariate functions, fs-LIBS conducts better quantification of

  15. Temperature dependence of the hydrated electron's excited-state relaxation. II. Elucidating the relaxation mechanism through ultrafast transient absorption and stimulated emission spectroscopy

    Science.gov (United States)

    Farr, Erik P.; Zho, Chen-Chen; Challa, Jagannadha R.; Schwartz, Benjamin J.

    2017-08-01

    The structure of the hydrated electron, particularly whether it exists primarily within a cavity or encompasses interior water molecules, has been the subject of much recent debate. In Paper I [C.-C. Zho et al., J. Chem. Phys. 147, 074503 (2017)], we found that mixed quantum/classical simulations with cavity and non-cavity pseudopotentials gave different predictions for the temperature dependence of the rate of the photoexcited hydrated electron's relaxation back to the ground state. In this paper, we measure the ultrafast transient absorption spectroscopy of the photoexcited hydrated electron as a function of temperature to confront the predictions of our simulations. The ultrafast spectroscopy clearly shows faster relaxation dynamics at higher temperatures. In particular, the transient absorption data show a clear excess bleach beyond that of the equilibrium hydrated electron's ground-state absorption that can only be explained by stimulated emission. This stimulated emission component, which is consistent with the experimentally known fluorescence spectrum of the hydrated electron, decreases in both amplitude and lifetime as the temperature is increased. We use a kinetic model to globally fit the temperature-dependent transient absorption data at multiple temperatures ranging from 0 to 45 °C. We find the room-temperature lifetime of the excited-state hydrated electron to be 137 ±40 fs, in close agreement with recent time-resolved photoelectron spectroscopy (TRPES) experiments and in strong support of the "non-adiabatic" picture of the hydrated electron's excited-state relaxation. Moreover, we find that the excited-state lifetime is strongly temperature dependent, changing by slightly more than a factor of two over the 45 °C temperature range explored. This temperature dependence of the lifetime, along with a faster rate of ground-state cooling with increasing bulk temperature, should be directly observable by future TRPES experiments. Our data also suggest

  16. Theoretical Modeling of Emission-Line galaxies: New Classification Parameters for Mid-Infrared and Optical Spectroscopy

    CERN Document Server

    Meléndez, M; Martínez-Paredes, M; Kraemer, S B; Mendoza, C

    2014-01-01

    We have carried out extensive and detailed photoionization modeling to successfully constrain the locations of different emission-line galaxies in optical and mid-infrared diagnostic diagrams. Our model grids cover a wide range in parameter space for the active galaxy continuum and starburst galaxies with different stellar population laws and metallicities. We compare the predicted AGN and star-formation mid-infrared line ratios [Ne III]15.56mm/[Ne II]12.81mm and [O IV]25.89mm/[Ne III]15.56mm to the observed values, and find that the best fit for the AGN is via a two-zone approximation. This two-zone approximation is a combination of a matter-bounded component, where [Ne III] and [O IV] are emitted efficiently, and a radiation-bounded component that maximizes [Ne II] emission. We overlay the predictions from this two-zone approximation onto the optical [O III]l5007/Hbeta and [N II]l6583/Halpha diagnostic diagram derived from the Sloan Digital Sky Survey, to find that the high-density and low-ionization radiat...

  17. Potential benefits of triethylamine as n-electron donor in the estimation of forskolin by electronic absorption and emission spectroscopy

    Science.gov (United States)

    Raju, Gajula; Ram Reddy, A.

    2016-02-01

    Diterpenoid forskolin was isolated from Coleus forskolii. The electronic absorption and emission studies of forskolin were investigated in various solvents with an aim to improve its detection limits. The two chromophores present in the diterpenoid are not conjugated leading to the poor absorption and emission of UV light. The absorption and fluorescence spectra were solvent specific. In the presence of a monodentate ligand, triethylamine the detection of forskolin is improved by 3.63 times in ethanol with the fluorescence method and 3.36 times in DMSO by the absorption spectral method. The longer wavelength absorption maximum is blue shifted while the lower energy fluorescence maximum is red shifted in the presence of triethylamine. From the wavelength of fluorescence maxima of the exciplex formed between excited forskolin and triethylamine it is concluded that the order of reactivity of hydroxyl groups in the excited state forskolin is in the reverse order to that of the order of the reactivity of hydroxyl groups in its ground state.

  18. Time-Resolved Optical Emission Spectroscopy Diagnosis of CO2 Laser-Produced SnO2 Plasma

    Science.gov (United States)

    Lan, Hui; Wang, Xinbing; Zuo, Duluo

    2016-09-01

    The spectral emission and plasma parameters of SnO2 plasmas have been investigated. A planar ceramic SnO2 target was irradiated by a CO2 laser with a full width at half maximum of 80 ns. The temporal behavior of the specific emission lines from the SnO2 plasma was characterized. The intensities of Sn I and Sn II lines first increased, and then decreased with the delay time. The results also showed a faster decay of Sn I atoms than that of Sn II ionic species. The temporal evolutions of the SnO2 plasma parameters (electron temperature and density) were deduced. The measured temperature and density of SnO2 plasma are 4.38 eV to 0.5 eV and 11.38×1017 cm-3 to 1.1×1017 cm-3, for delay times between 0.1 μs and 2.2 μs. We also investigated the effect of the laser pulse energy on SnO2 plasma. supported by National Natural Science Foundation of China (No. 11304235) and the Director Fund of WNLO

  19. Programs in Fortran language for reporting the results of the analyses by ICP emission spectroscopy; Programas en lenguaje Fortran para la informacion de los resultados de los analisis efectuados mediante Espectroscopia Optica de emision con fuente de plasma

    Energy Technology Data Exchange (ETDEWEB)

    Roca, M.

    1985-07-01

    Three programs, written in FORTRAN IV language, for reporting the results of the analyses by ICP emission spectroscopy from data stored in files on floppy disks have been developed. They are intended, respectively, for the analyses of: 1) waters, 2) granites and slates, and 3) different kinds of geological materials. (Author) 8 refs.

  20. Diagnosis of the local thermal equilibrium by optical emission spectroscopy in the evolution of electric discharge; Diagnostico del equilibrio termico local por espectroscopia optica de emision en la evolucion de una descarga electrica

    Energy Technology Data Exchange (ETDEWEB)

    Valdivia B, R.; Pacheco S, J.; Pacheco P, M.; Ramos F, F.; Cruz A, A. [ININ, Carretera Mexico-Toluca s/n, Ocoyoacac 52750, Estado de Mexico (Mexico); Velazquez P, S. [Instituto Tecnologico de Toluca, Av. Instituto Tecnologico s/n, Ex-Rancho la Virgen, Metepec 52140, Estado de Mexico (Mexico)

    2008-07-01

    In this work applies the technique of optical emission spectroscopy to diagnose the temperature of the species generated in plasma in the transition to glow discharge arc. Whit this diagnosis is possible to determine the local thermal equilibrium conditions of the discharge. (Author)

  1. Probing Pulsar Emission on Short Timescales: Rotating Radio Transients, Cyclic Spectroscopy, and Single-Pulse Studies of Millisecond Pulsars

    Science.gov (United States)

    Palliyaguru, Nipuni Tharaka

    Rotating radio transients (RRATs) are neutron stars are that characterized by the emission of strong sporadic bursts. We have analysed the long- and short-term time dependence of the pulse arrival times and the pulse detection rates for eight RRAT sources from the Parkes Multi-beam Pulsar Survey (PMPS). We find significant periodicities in the individual pulse arrival times from six RRATs. These periodicities range from ˜30 minutes to 2100 days and from one to 16 independent (i.e. non-harmonically related) periodicities are detected for each RRAT. In addition, we find that pulse emission is a random process on short (hour-long) time scales but that most of the objects exhibit longer term (months-years) non-random behaviour. We find that PSRs J1819--1458 and J1317--5759 emit more doublets (two consecutive pulses) and triplets (three consecutive pulses) than is expected in random pulse distributions. No evidence for such an excess is found for the other RRATs. There are several different models for RRAT emission depending on both extrinsic and intrinsic factors which are consistent with these properties. Light travel time changes due to gravitational waves may be detected within the next decade through precision timing of an array of millisecond pulsars. Removal of frequency-dependent interstellar medium (ISM) delays due to dispersion and scattering is a key issue in the detection process. Current timing algorithms routinely correct pulse times of arrival (TOAs) for time-variable delays due to cold plasma dispersion. However, none of the major pulsar timing groups routinely correct for delays due to scattering from multi-path propagation in the ISM. Scattering introduces a phase change in the signal that results in pulse broadening and arrival time delays. As a step toward a more comprehensive ISM propagation delay correction, we demonstrate through a simulation that we can accurately recover pulse broadening functions (PBFs), such as those that would be introduced

  2. Visible-near infrared spectroscopy as a tool to improve mapping of soil properties

    Science.gov (United States)

    Evgrafova, Alevtina; Kühnel, Anna; Bogner, Christina; Haase, Ina; Shibistova, Olga; Guggenberger, Georg; Tananaev, Nikita; Sauheitl, Leopold; Spielvogel, Sandra

    2017-04-01

    Spectroscopic measurements, which are non-destructive, precise and rapid, can be used to predict soil properties and help estimate the spatial variability of soil properties at the pedon scale. These estimations are required for quantifying soil properties with higher precision, identifying the changes in soil properties and ecosystem response to climate change as well as increasing the estimation accuracy of soil-related models. Our objectives were to (i) predict soil properties for nested samples (n = 296) using the laboratory-based visible-near infrared (vis-NIR) spectra of air-dried (Germany). Inorganic C was removed from the mineral soil samples with pH values higher than 7 prior to the elemental analysis using the volatilization method (HCl, 6 hours). The pH of soil samples was measured in 0.01 M CaCl2 using a 1:2 soil:solution ratio. However, for soil sample with a high in organic matter content, a 1:10 ratio was applied. We also measured oxalate and dithionite extracted iron, aluminum and manganese oxides and hydroxides using inductively coupled plasma optical emission spectroscopy (Varian Vista MPX ICP-OES, Agilent Technologies, USA). We predicted the above-mentioned soil properties for all nested samples using partial least squares regression, which was performed using R program. We can conclude that vis-NIR spectroscopy can be used effectively in order to describe, estimate and further map the spatial patterns of soil properties using geostatistical methods. This research could also help to improve the global soil spectral library taking into account that only few previous applications of vis-NIR spectroscopy were conducted on permafrost-affected soils of Northern Siberia. Keywords: Visible-near infrared spectroscopy, vis-NIR, permafrost-affected soils, Siberia, partial least squares regression.

  3. Benchmark Results and Theoretical Treatments for Valence-to-Core X-ray Emission Spectroscopy in Transition Metal Compounds

    Energy Technology Data Exchange (ETDEWEB)

    Mortensen, Devon R.; Seidler, Gerald T.; Kas, Joshua J.; Govind, Niranjan; Schwartz, Craig; Pemmaraju, Das; Prendergast, David

    2017-09-20

    We report measurement of the valence-to-core (VTC) region of the K-shell x-ray emission spectra from several Zn and Fe inorganic compounds, and their critical comparison with several existing theoretical treatments. We find generally good agreement between the respective theories and experiment, and in particular find an important admixture of dipole and quadrupole character for Zn materials that is much weaker in Fe-based systems. These results on materials whose simple crystal structures should not, a prior, pose deep challenges to theory, will prove useful in guiding the further development of DFT and time-dependent DFT methods for VTC-XES predictions and their comparison to experiment.

  4. Time resolved study of the emission enhancement mechanisms in orthogonal double-pulse laser-induced breakdown spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Sanginés, R., E-mail: roberto.sangines@ccadet.unam.mx; Sobral, H.

    2013-10-01

    The evolution of laser induced ablation plume on aluminum targets has been investigated in orthogonal pre-ablation double pulse scheme at atmospheric pressure from the earliest stages of plasma evolution. Time-resolved emission spectra from neutrals, singly- and doubly-ionized species obtained with the double pulse experiment have been compared with those from the single pulse configuration. Signal-to-noise enhancement reaches values of up to 15 depending on the analyzed species; and the lower the charge state the later its maximum signal-to-noise ratio is reached. Ablation plume dynamics was monitored from 10 ns after the plasma onset via shadowgraphy and fast-photography with narrow interference filters to follow the evolution of individual species. Results show that ionic species from the target are located at the plasma core while nitrogen from the background air is found at the plume peripheral. Initially both configurations exhibit similar ablation plume sizes and their expansions were successfully fitted with the strong explosion model for the first 500 ns. At later times a good agreement was obtained by using the drag model, which predicts that the plume expansion eventually stops due to interaction with the background gas particles. The emission enhancement measured in the double pulse scheme is discussed in terms of the models describing the plume dynamics. - Highlights: • Production of 2 + ions at the earliest stages of plasma evolution • The higher the charge state the inner the location within the ablation plume. • The expansion rate of the second (ablation) plume was measured. • Shock and drag models successfully fit the ablation shock front expansion.

  5. Electronic structure and characteristics of Fe 3d valence states of Fe(1.01)Se superconductors under pressure probed by x-ray absorption spectroscopy and resonant x-ray emission spectroscopy.

    Science.gov (United States)

    Chen, J M; Haw, S C; Lee, J M; Chen, S A; Lu, K T; Deng, M J; Chen, S W; Ishii, H; Hiraoka, N; Tsuei, K D

    2012-12-28

    The electronic structure and characteristics of Fe 3d valence states of iron-chalcogenide Fe(1.01)Se superconductors under pressure were probed with x-ray absorption spectroscopy and resonant x-ray emission spectroscopy (RXES). The intensity of the pre-edge peak at ~7112.7 eV of the Fe K-edge x-ray absorption spectrum of Fe(1.01)Se decreases for pressure from 0.5 GPa increased to 6.9 GPa. The satellite line Kβ' was reduced in intensity upon applying pressure and became absent for pressure 52 GPa. Fe(1.01)Se shows a small net magnetic moment of Fe(2+), likely arising from strong Fe-Fe spin fluctuations. The 1s3p-RXES spectra of Fe(1.01)Se at pressures 0.5, 6.9, and 52 GPa recorded at the Fe K-edge reveal that unoccupied Fe 3d states exhibit a delocalized character, stemming from hybridization of Fe 3d and 4p orbitals arising from a local distortion around the Fe atom in a tetrahedral site. Application of pressure causes suppression of this on-site Fe 3d-Fe 4p hybridization, and thereby decreases the intensity of the pre-edge feature in the Fe K-edge absorption spectrum of Fe(1.01)Se. Compression enhances spin fluctuations at Fe sites in Fe(1.01)Se and increases the corresponding T(c), through a competition between nearest-neighbor ferromagnetic and next-nearest-neighbor antiferromagnetic superexchange interactions. This result aids our understanding of the physics underlying iron-based superconductors.

  6. Time-resolved OES of nanosecond pulsed discharges in N$_{2}$ and N$_{2}$/H$_{2}$O mixtures]{Time-resolved optical emission spectroscopy of nanosecond pulsed discharges in atmospheric pressure N$_{2}$ and N$_{2}$/H$_{2}$O mixtures

    CERN Document Server

    van der Horst, R M; van Veldhuizen, E M; Bruggeman, P J

    2014-01-01

    In this contribution, nanosecond pulsed discharges in N$_{2}$ and N$_{2}$/0.9% H$_{2}$O at atmospheric pressure (at 300 K) are studied with time-resolved imaging, optical emission spectroscopy and Rayleigh scattering. A 170 ns high voltage pulse is applied across two pin-shaped electrodes at a frequency of 1 kHz. The discharge consists of three phases: an ignition phase, a spark phase and a recombination phase. During the ignition phase the emission is mainly caused by molecular nitrogen (N$_{2}$(C-B)). In the spark and recombination phase mainly atomic nitrogen emission is observed. The emission when H$_{2}$O is added is very similar, except the small contribution of H$_{\\alpha}$ and the intensity of the molecular N$_{2}$(C-B) emission is less.

  7. Predicting methane emissions of lactating Danish Holstein cows using Fourier transform mid-infrared spectroscopy of milk.

    Science.gov (United States)

    Shetty, N; Difford, G; Lassen, J; Løvendahl, P; Buitenhuis, A J

    2017-09-13

    Enteric methane (CH4), a potent greenhouse gas, is among the main targets of mitigation practices for the dairy industry. A measurement technique that is rapid, inexpensive, easy to use, and applicable at the population level is desired to estimate CH4 emission from dairy cows. In the present study, feasibility of milk Fourier transform mid-infrared (FT-IR) spectral profiles as a predictor for CH4:CO2 ratio and CH4 production (L/d) is explained. The partial least squares regression method was used to develop the prediction models. The models were validated using different random test sets, which are independent from the training set by leaving out records of 20% cows for validation and keeping records of 80% of cows for training the model. The data set consisted of 3,623 records from 500 Danish Holstein cows from both experimental and commercial farms. For both CH4:CO2 ratio and CH4 production, low prediction accuracies were found when models were obtained using FT-IR spectra. Validated coefficient of determination (R(2)Val) = 0.21 with validated model error root mean squared error of prediction (RMSEP) = 0.0114 L/d for CH4:CO2 ratio, and R(2)Val = 0.13 with RMSEP = 111 L/d for CH4 production. The important spectral wavenumbers selected using the recursive partial least squares method represented major milk components fat, protein, and lactose regions of the spectra. When fat and protein predicted by FT-IR were used instead of full spectra, a low R(2)Val of 0.07 was obtained for both CH4:CO2 ratio and CH4 production prediction. Other spectral wavenumbers related to lactose (carbohydrate) or additional wavenumbers related to fat or protein (amide II) are providing additional variation when using the full spectral profile. For CH4:CO2 ratio prediction, integration of FT-IR with other factors such as milk yield, herd, and lactation stage showed improvement in the prediction accuracy. However, overall prediction accuracy remained modest; R(2)Val increased to 0.31 with

  8. Quantitative analysis of soil calcium by laser-induced breakdown spectroscopy using addition and addition-internal standardizations

    Science.gov (United States)

    Shirvani-Mahdavi, Hamidreza; Shafiee, Parisa

    2016-12-01

    Matrix mismatching in the quantitative analysis of materials through calibration-based laser-induced breakdown spectroscopy (LIBS) is a serious problem. In this paper, to overcome the matrix mismatching, two distinct approaches named addition standardization (AS) and addition-internal combinatorial standardization (A-ICS) are demonstrated for LIBS experiments. Furthermore, in order to examine the efficiency of these methods, the concentration of calcium in ordinary garden soil without any fertilizer is individually measured by each of the two procedures. To achieve this purpose, ten standard samples with different concentrations of calcium (as the analyte) and copper (as the internal standard) are prepared in the form of cylindrical tablets, so that the soil plays the role of the matrix in all of them. The measurements indicate that the relative error of concentration compared to a certified value derived by induced coupled plasma optical emission spectroscopy is 3.97% and 2.23% for AS and A-ICS methods, respectively. Furthermore, calculations related to standard deviation indicates that A-ICS method may be more accurate than AS one.

  9. Lunar Mare Basalts as Analogues for Martian Volcanic Compositions: Evidence from Visible, Near-IR, and Thermal Emission Spectroscopy

    Science.gov (United States)

    Graff, T. G.; Morris, R. V.; Christensen, P. R.

    2003-01-01

    The lunar mare basalts potentially provide a unique sample suite for understanding the nature of basalts on the martian surface. Our current knowledge of the mineralogical and chemical composition of the basaltic material on Mars comes from studies of the basaltic martian meteorites and from orbital and surface remote sensing observations. Petrographic observations of basaltic martian meteorites (e.g., Shergotty, Zagami, and EETA79001) show that the dominant phases are pyroxene (primarily pigeonite and augite), maskelynite (a diaplectic glass formed from plagioclase by shock), and olivine [1,2]. Pigeonite, a low calcium pyroxene, is generally not found in abundance in terrestrial basalts, but does often occur on the Moon [3]. Lunar samples thus provide a means to examine a variety of pigeonite-rich basalts that also have bulk elemental compositions (particularly low-Ti Apollo 15 mare basalts) that are comparable to basaltic SNC meteorites [4,5]. Furthermore, lunar basalts may be mineralogically better suited as analogues of the martian surface basalts than the basaltic martian meteorites because the plagioclase feldspar in the basaltic Martian meteorites, but not in the lunar surface basalts, is largely present as maskelynite [1,2]. Analysis of lunar mare basalts my also lead to additional endmember spectra for spectral libraries. This is particularly important analysis of martian thermal emission spectra, because the spectral library apparently contains a single pigeonite spectrum derived from a synthetic sample [6].

  10. Spatial and Temporal characterization of plasma properties via emission spectroscopy in fusion materials testing device Proto-MPEX

    Science.gov (United States)

    Morean, Casey; Biewer, Theodore; Shaw, Guinevere; Beers, Josh; Ray, Holly

    2016-10-01

    The Prototype Material Plasma Exposure eXperiment (Proto-MPEX) is a linear plasma source, and is intended to study plasma-material interactions (PMI) in conditions similar to those found in future fusion reactors. A high-resolution McPherson Czerny-Turner visible range spectrometer has been utilized to study the behavior of ions in the plasma. Analysis of the spectral lines, D_beta, D_gamma, and D_delta yields valuable information regarding the temperature and density of plasma ions at various locations along Proto-MPEX. Spectroscopic temperature and density measurements are compared to double Langmuir probe measurements to determine plasma behavior as a function of radius. Temporal and spatial measurements along the length of Proto-MPEX are constructed and compared to a photomultiplier tube based diagnostic manufactured at ORNL to determine the plasma's axial behavior along Proto-MPEX. Relative emission of beta, gamma, and delta lines are used to assess recycling effects in the device. This work was supported by the U.S. D.O.E. contract DE-AC05-00OR22725.

  11. Depth profiling of thin film solar cell components by synchrotron excited Soft X-ray emission spectroscopy (SXES)

    Energy Technology Data Exchange (ETDEWEB)

    Moenig, Harry; Grimm, Alexander; Lux-Steiner, Martha; Saez-Araoz, Rodrigo; Fischer, Christian-Herbert [Freie Universitaet Berlin (Germany); Baer, Markus [University of Las Vegas (United States); Camus, Christian; Ennaoui, Ahmed; Kaufmann, Christian; Koerber, Paul; Kropp, Timo; Lauermann, Iver; Lehmann, Sebastian; Muenchenberg, Tim; Pistor, Paul; Puttnins, Stefan; Schock, Hans-Werner; Sokoll, Stefan [Hahn-Meitner-Institut Berlin (Germany); Jung, Christian [BESSY GmbH Berlin (Germany)

    2007-07-01

    Depending on the elemental composition of a material, SXES provides an information depth of 50-1000 nm. For studies of thin multilayer structures tuning of this parameter is highly desirable. One possibility is the variation of the excitation energy, which is accompanied by variation of photoionisation cross sections. Alternatively, we performed angle resolved SXES on the solar cell absorber material Cu(In,Ga)Se{sub 2} covered by CdS or Zn(S,O) buffer layers (10-50 nm). Due to our setup geometry, the emission spectra clearly display increased surface sensitivity at small (grazing exit) and large (grazing incidence) exit angles. A model based on Beer-Lamberts law and setup geometry is in reasonable agreement with our experimental data.The presented results show that angle resolved SXES measurements yield depth-dependent information on multilayer structures. The increased surface sensitivity at grazing exit and grazing incidence angles allows the detection of extremely thin cover layers at reasonable recording times.

  12. Stack emission monitoring using non-dispersive infrared spectroscopy with an optimized nonlinear absorption cross interference correction algorithm

    Directory of Open Access Journals (Sweden)

    Y. W. Sun

    2013-08-01

    Full Text Available In this paper, we present an optimized analysis algorithm for non-dispersive infrared (NDIR to in situ monitor stack emissions. The proposed algorithm simultaneously compensates for nonlinear absorption and cross interference among different gases. We present a mathematical derivation for the measurement error caused by variations in interference coefficients when nonlinear absorption occurs. The proposed algorithm is derived from a classical one and uses interference functions to quantify cross interference. The interference functions vary proportionally with the nonlinear absorption. Thus, interference coefficients among different gases can be modeled by the interference functions whether gases are characterized by linear or nonlinear absorption. In this study, the simultaneous analysis of two components (CO2 and CO serves as an example for the validation of the proposed algorithm. The interference functions in this case can be obtained by least-squares fitting with third-order polynomials. Experiments show that the results of cross interference correction are improved significantly by utilizing the fitted interference functions when nonlinear absorptions occur. The dynamic measurement ranges of CO2 and CO are improved by about a factor of 1.8 and 3.5, respectively. A commercial analyzer with high accuracy was used to validate the CO and CO2 measurements derived from the NDIR analyzer prototype in which the new algorithm was embedded. The comparison of the two analyzers show that the prototype works well both within the linear and nonlinear ranges.

  13. Laser optogalvanic spectroscopy of neon in a discharge plasma and modeling and analysis of rocket plume RF-line emissions

    Science.gov (United States)

    Ogungbemi, Kayode I.

    databases (e.g. JPL/NASA and Cologne), together with other appropriate spectroscopic data. Hydrazine fuel was selected as the rocket propellant of choice and the plume codes were run by the JHU-APL research group. A representative monopropellant hydrazine plume has been determined to provide exhaust temperature, pressure, velocity, and species number density inputs for model development. A MATLAB code has been developed for computing broadside line-of-sight (LOS) intensities due to line emissions involving ammonia and other plume species. Initially, we assumed Local Thermodynamic Equilibrium (LTE) and included self-absorption contributions due to plume opacity, together with collisional and Doppler broadening, as well as the Doppler shift due to the plume radial velocity towards and away from a stationary detector. The recorded code output was MATLAB coded and an assortment of plume parameters computed, such as the volume emission rate, the absorption coefficient, optical depth and species radiance line-by-line. These parameters were computed both manually utilizing a spread sheet and then automated using the Matlab code. The volume emissions, along with other plume properties, were plotted as a function of the axial distance in the plume for several Radio Frequency (RF) transitions involving various significant plume species. Plume properties, such as the temperature, pressure, number density, and plume particulate speed emanating from the nozzle where analyzed and modeled as the plume drifts away from the rocket nozzle. Both the axial and radial distance dependences were investigated with respect to the various plume properties and parameters. Population distribution of the species (number density) dependence on the plume temperature was investigated and modeled line-by-line for each of the plume species studied at the nozzle exit plane and beyond. In addition, volume emission and absorption coefficients have been analyzed and modeled and solutions to the Radiative

  14. Magnetic and structural properties of manganese doped (Al,Ga)N studied with emission Mössbauer spectroscopy

    CERN Multimedia

    Gallium nitride (GaN) and related compounds form a unique class of semiconductors with extraordinary qualities in terms of their crystal structure, optical properties, and electrical properties. These novel properties have made them useful in a wide range of applications in optoelectronic and high-frequency devices such as light emitting diodes, laser diodes and high power field effect transistors. When doped with a few percents of Mn and in the presence of free holes, GaN has been predicted to be a magnetic semiconductor with Curie temperature above room temperature. Mixed semiconductors of Al$_{x}$Ga$_{1-x}$N (AlGaN) composition, give rise to unexpected and critical magnetic and photonic functionalities when doped with magnetic ion species. Here we propose an experiment on very thoroughly characterised AlGaN doped with Mn utilising extremely dilute $^{57}$Mn (T$_{1/2}$=1.5 min), $^{57}$Co (T$_{1/2}$ = 272 d) and $^{119}$In (T$_{1/2}$=2.1 min) implantations, in order to perform $^{57}$Fe and $^{119}$Sn emiss...

  15. In-situ optical emission spectroscopy for a better control of hybrid sputtering/evaporation process for the deposition of Cu(In,Ga)Se{sub 2} layers

    Energy Technology Data Exchange (ETDEWEB)

    Posada, Jorge; Jubault, Marie [Institute of Research and Development on Photovoltaic Energy (IRDEP), EDF-CNRS-Chimie ParisTech, UMR 7174, 6 Quai Watier, 78401 Chatou (France); Bousquet, Angélique; Tomasella, Eric [Clermont Université, Université Blaise Pascal, Institute of Chemistry of Clermont-Ferrand (ICCF), CNRS-UMR 6296, 24 Avenue des Landais, 63171 Aubière (France); Lincot, Daniel [Institute of Research and Development on Photovoltaic Energy (IRDEP), EDF-CNRS-Chimie ParisTech, UMR 7174, 6 Quai Watier, 78401 Chatou (France)

    2015-05-01

    In this work, we have developed a hybrid one-step co-sputtering/evaporation Cu(In,Ga)Se{sub 2} (CIGS) process, where Cu, In and Ga are sputtered simultaneously with the thermal evaporation of selenium, thus avoiding the H{sub 2}Se use. An appropriate control of the selenium flux is very important to prevent the target poisoning and hence some material flux variations. Indeed, the control of the CIGS composition must be rigorous to ensure reproducible solar cell properties. In this regard, a study of the correlations between plasma species and thin film composition, structure and morphology has been performed by varying power values and Se evaporation temperature in the 170 to 230 °C range. We started by studying the plasma with a powerful technique: optical emission spectroscopy, following light emissions from different plasma species: sputtered Cu, Ga, In but also evaporated Se. Hence, we determined the Se flow threshold avoiding target poisoning and the main parameter controlling the CIGS composition. Obviously, we also focused our interest on the material. We measured film composition and thickness of the samples with X-ray fluorescence and by energy dispersive X-ray. Different phases formed during the process were identified by Raman spectroscopy and X-ray diffraction. The optoelectronic cell properties showed promising efficiency of 10.3% for an absorber with composition ratios of [Cu]/([In] + [Ga]) = 1.02 and [Ga]/([In] + [Ga]) = 0.44. Finally, this work shows that we are able to control this hybrid process and thus the structure and composition of CIGS thin film for industrial transfer in the photovoltaic field. - Highlights: • We have developed a hybrid one-step co-sputtering/evaporation Cu(In,Ga)Se{sub 2} process. • Correlations between plasma species and thin film composition have been performed. • We determined the Se flow threshold avoiding target poisoning. • Efficient small-area CIGS cells with 10.3% efficiency were fabricated.

  16. Basaltic glass formed from hydrovolcanism and impact processes: Characterization and clues for detection of mode of origin from VNIR through MWIR reflectance and emission spectroscopy

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