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Sample records for analytical atomic emission

  1. Expressing self-absorption in the analytical function of inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Kántor, Tibor; Bartha, András

    2015-11-01

    The self-absorption of spectral lines was studied with up to date multi-element inductively coupled plasma atomic emission spectrometry (ICP-AES) instrumentation using radial and axial viewing of the plasma, as well, performing line peak height and line peak area measurements. Two resonance atomic and ionic lines of Cd and Mg were studied, the concentration range was extended up to 2000 mg/L. At the varying analyte concentration, constant matrix concentration of 10,000 mg/L Ca was ensured in the pneumatically nebulized solutions. The physical and the phenomenological formulation of the emission analytical function is overviewed and as the continuity of the earlier results the following equation is offered:

  2. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry

    NASA Astrophysics Data System (ADS)

    Montaser, A.

    In this project, new high temperature plasmas and new sample introduction systems are developed for rapid elemental and isotopic analysis of gases, solutions, and solids using atomic emission spectrometry (AES) and mass spectrometry (MS). These devices offer promise of solving singularly difficult analytical problems that either exist now or are likely to arise in the future in the various fields of energy generation, environmental pollution, nutrition, and biomedicine. Emphasis is being placed on: (1) generation of annular, helium inductively coupled plasmas (He ICPs) that are suitable for atomization, excitation, and ionization of elements possessing high excitation and ionization energies, with the intent of enhancing the detecting powers of a number of elements; (2) computer modelings of ICP discharges to predict the behavior of new and existing plasmas; (3) diagnostic studies of high temperature plasmas and sample introduction systems to quantify their fundamental properties, with the ultimate aim to improve analytical performance of atomic spectrometry; (4) development and characterization of new, low cost sample introduction systems that consume microliter or microgram quantities of samples; and (5) investigation of new membrane separators for stripping solvent from sample aerosol to reduce various interferences and to enhance sensitivity and selectivity in plasma spectrometry.

  3. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry

    SciTech Connect

    Montaser, A.

    1990-01-01

    In this project, new high temperature plasmas and new sample introduction systems are developed for rapid elemental and isotopic analysis of gases, solutions, and solids using atomic emission spectrometry (AES) and mass spectrometry (MS). These devices offer promise of solving singularly difficult analytical problems that either exist now or are likely to arise in the future in the various fields of energy generation, environmental pollution, biomedicine and nutrition. Emphasis is being placed on: generation of annular, helium inductively coupled plasmas (He ICPs) that are suitable for atomization, excitation, and ionization of elements possessing high excitation and ionization energies, with the intent of enhancing the detecting powers of a number of elements; diagnostic studies of high-temperature plasmas to quantify their fundamental properties, with the ultimate aim to improve analytical performance of atomic spectrometry; development and characterization of new sample introduction systems that consume microliter or microgram quantities of samples, and investigation of new membrane separators for striping solvent from sample aerosol to reduce various interferences and to enhance sensitivity in plasma spectrometry.

  4. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry

    SciTech Connect

    Montaser, A.

    1992-01-01

    New high temperature plasmas and new sample introduction systems are explored for rapid elemental and isotopic analysis of gases, solutions, and solids using mass spectrometry and atomic emission spectrometry. Emphasis was placed on atmospheric pressure He inductively coupled plasmas (ICP) suitable for atomization, excitation, and ionization of elements; simulation and computer modeling of plasma sources with potential for use in spectrochemical analysis; spectroscopic imaging and diagnostic studies of high temperature plasmas, particularly He ICP discharges; and development of new, low-cost sample introduction systems, and examination of techniques for probing the aerosols over a wide range. Refs., 14 figs. (DLC)

  5. Differentiation of colloidal and dissolved silica: Analytical separation using spectrophotometry and inductively coupled plasma atomic emission spectrometry

    USGS Publications Warehouse

    Lewis-Russ, A.; Ranville, J.; Kashuba, A.T.

    1991-01-01

    A method is described that differentiates between solutions containing silica-dominated colloids and solutions that are essentially free of colloids. Suspensions of tuff particles were treated to remove colloids by centrifugation, filtration or both. Agreement of silica concentrations determined by inductively coupled plasma atomic emission spectrometry and by a spectrophotometric method was taken as an indication of colloid-free solutions. For two tuffs, centrifugation was effective for removing colloids. For the third, highly altered tuff, filtration was more effective for removing colloids.

  6. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Progress report: January 1, 1993--December 31, 1993

    SciTech Connect

    Montaser, A.

    1993-12-31

    In this research, new high-temperature plasmas and new sample introduction systems are explored for rapid elemental and isotopic analysis of gases, solutions, and solids using mass spectrometry and atomic emission spectrometry. During the period January 1993--December 1993, emphasis was placed on (a) analytical investigations of atmospheric-pressure helium inductively coupled plasma (He ICP) that are suitable for atomization, excitation, and ionization of elements possessing high excitation and ionization energies; (b) simulation and computer modeling of plasma sources to predict their structure and fundamental and analytical properties without incurring the enormous cost of experimental studies; (c) spectrosopic imaging and diagnostic studies of high-temperature plasmas; (d) fundamental studies of He ICP discharges and argon-nitrogen plasma by high-resolution Fourier transform spectrometry; and (e) fundamental and analytical investigation of new, low-cost devices as sample introduction systems for atomic spectrometry and examination of new diagnostic techniques for probing aerosols. Only the most important achievements are included in this report to illustrate progress and obstacles. Detailed descriptions of the authors` investigations are outlined in the reprints and preprints that accompany this report. The technical progress expected next year is briefly described at the end of this report.

  7. Selection of operating conditions and analytical procedure in multi-metal analysis of animal tissues by d.c. plasma-atomic emission spectroscopy

    NASA Astrophysics Data System (ADS)

    Frank, Adrian; Petersson, Lars R.

    In order to expand the analytical capacity and achieve better utilization of tissue materials (liver, kidney, etc.) so as to assess the degrees of environmental pollution, a method for simultaneous determination of 14 metals (Al, Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Ni, Pb, V, W, and Zn) has been developed by applying d.c. plasma-atomic emission spectroscopy. The analytical emission lines were chosen after considering the absence of more important interfering emission lines from elements present in the matrix, and taking into account their intensity, background, range of linearity and working range. At increasing ionic buffer concentration most metals seem to have a region of relatively little change in intensity. A 0.25 M LiNO 3 solution was chosen as ionic buffer. Optimization of plasma position to obtain maximum light intensity at each of the analytical wavelengths was studied with both single- and multi-element cassettes. The intention was to find a plasma position with satisfactory light intensity for all metals to be determined simultaneously. Spectral interferences, stray light effects included, from elements present in the matrix were investigated and linear relationships were usually found between the "false" signal contribution and the concentration of the interfering element. These signals were expressed as spectral interference correction coefficients (SICC values) on a concentration equivalent basis, viz. μ ml -1 per μ ml -1. The effect of Ca on the analytical emission lines of Al, Pb, and W was not linear in contrast to the usual relationship. Organ tissues are prepared by automated wet digestion. Transfer of sample solution from the sample tray into the plasma is performed automatically. A microcomputer is used for evaluation of metal contents in the solutions, background correction by use of SICC values, and final calculation of metal concentrations in the tissues.

  8. Comparison in the analytical performance between krypton and argon glow discharge plasmas as the excitation source for atomic emission spectrometry.

    PubMed

    Wagatsuma, Kazuaki

    2009-04-01

    The emission characteristics of ionic lines of nickel, cobalt, and vanadium were investigated when argon or krypton was employed as the plasma gas in glow discharge optical emission spectrometry. A dc Grimm-style lamp was employed as the excitation source. Detection limits of the ionic lines in each iron-matrix alloy sample were compared between the krypton and the argon plasmas. Particular intense ionic lines were observed in the emission spectra as a function of the discharge gas (krypton or argon), such as the Co II 258.033 nm for krypton and the Co II 231.707 nm for argon. The explanation for this is that collisions with the plasma gases dominantly populate particular excited levels of cobalt ion, which can receive the internal energy from each gas ion selectively, for example, the 3d(7)4p (3)G(5) (6.0201 eV) for krypton and the 3d(7)4p (3)G(4) (8.0779 eV) for argon. In the determination of nickel as well as cobalt in iron-matrix samples, more sensitive ionic lines could be found in the krypton plasma rather than the argon plasma. Detection limits in the krypton plasma were 0.0039 mass% Ni for the Ni II 230.299-nm line and 0.002 mass% Co for the Co II 258.033-nm line. However, in the determination of vanadium, the argon plasma had better analytical performance, giving a detection limit of 0.0023 mass% V for the V II 309.310-nm line.

  9. Analytical performance of a low-gas-flow torch optimized for inductively coupled plasma atomic emission spectrometry

    USGS Publications Warehouse

    Montaser, A.; Huse, G.R.; Wax, R.A.; Chan, S.-K.; Golightly, D.W.; Kane, J.S.; Dorrzapf, A.F.

    1984-01-01

    An inductively coupled Ar plasma (ICP), generated in a lowflow torch, was investigated by the simplex optimization technique for simultaneous, multielement, atomic emission spectrometry (AES). The variables studied included forward power, observation height, gas flow (outer, intermediate, and nebulizer carrier) and sample uptake rate. When the ICP was operated at 720-W forward power with a total gas flow of 5 L/min, the signal-to-background ratios (S/B) of spectral lines from 20 elements were either comparable or inferior, by a factor ranging from 1.5 to 2, to the results obtained from a conventional Ar ICP. Matrix effect studies on the Ca-PO4 system revealed that the plasma generated in the low-flow torch was as free of vaporizatton-atomizatton interferences as the conventional ICP, but easily ionizable elements produced a greater level of suppression or enhancement effects which could be reduced at higher forward powers. Electron number densities, as determined via the series until line merging technique, were tower ht the plasma sustained in the low-flow torch as compared with the conventional ICP. ?? 1984 American Chemical Society.

  10. Atomic hydrogen emission induced by TEA CO(2) laser bombardment on solid samples at low pressure and its analytical application.

    PubMed

    Idris, Nasrullah; Terai, Sumito; Lie, Tjung Jie; Kurniawan, Hendrik; Kobayashi, Takao; Maruyama, Tadashi; Kagawa, Kiichiro

    2005-01-01

    Hydrogen emission has been studied in laser plasmas by focusing a TEA CO(2) laser (10.6 microm, 500 mJ, 200 ns) on various types of samples, such as glass, quartz, black plastic sheet, and oil on copper plate sub-target. It was found that H(alpha) emission with a narrow spectral width occurs with high efficiency when the laser plasma is produced in the low-pressure region. On the contrary, the conventional well-known laser-induced breakdown spectroscopy (LIBS), which is usually carried out at atmospheric air pressure, cannot be applied to the analysis of hydrogen as an impurity. By combining low-pressure laser-induced plasma spectroscopy with laser surface cleaning, a preliminary quantitative analysis was made on zircaloy pipe samples intentionally doped with hydrogen. As a result, a good linear relationship was obtained between H(alpha) emission intensity and its concentration.

  11. Single atom electrochemical and atomic analytics

    NASA Astrophysics Data System (ADS)

    Vasudevan, Rama

    In the past decade, advances in electron and scanning-probe based microscopies have led to a wealth of imaging and spectroscopic data with atomic resolution, yielding substantial insight into local physics and chemistry in a diverse range of systems such as oxide catalysts, multiferroics, manganites, and 2D materials. However, typical analysis of atomically resolved images is limited, despite the fact that image intensities and distortions of the atoms from their idealized positions contain unique information on the physical and chemical properties inherent to the system. Here, we present approaches to data mine atomically resolved images in oxides, specifically in the hole-doped manganite La5/8Ca3/8MnO3, on epitaxial films studied by in-situ scanning tunnelling microscopy (STM). Through application of bias to the STM tip, atomic-scale electrochemistry is demonstrated on the manganite surface. STM images are then further analyzed through a suite of algorithms including 2D autocorrelations, sliding window Fourier transforms, and others, and can be combined with basic thermodynamic modelling to reveal relevant physical and chemical descriptors including segregation energies, existence and strength of atomic-scale diffusion barriers, surface energies and sub-surface chemical species identification. These approaches promise to provide tremendous insights from atomically resolved functional imaging, can provide relevant thermodynamic parameters, and auger well for use with first-principles calculations to yield quantitative atomic-level chemical identification and structure-property relations. This research was sponsored by the Division of Materials Sciences and Engineering, BES, DOE. Research was conducted at the Center for Nanophase Materials Sciences, which also provided support and is a DOE Office of Science User Facility.

  12. An analytical method for hydrogeochemical surveys: Inductively coupled plasma-atomic emission spectrometry after using enrichment coprecipitation with cobalt and ammonium pyrrolidine dithiocarbamate

    USGS Publications Warehouse

    Hopkins, D.M.

    1991-01-01

    Trace metals that are commonly associated with mineralization were concentrated and separated from natural water by coprecipitation with ammonium pyrollidine dithiocarbamate (APDC) and cobalt and determined by inductively coupled plasma-atomic emission spectroscopy (ICP-AES). The method is useful in hydrogeochemical surveys because it permits preconcentration near the sample sites, and selected metals are preserved shortly after the samples are collected. The procedure is relatively simple: (1) a liter of water is filtered; (2) the pH is adjusted; (3) Co chloride and APDC are added to coprecipitate the trace metals; and (4) later, the precipitate is filtered, dissolved, and diluted to 10 ml for a 100-fold concentration enrichment of the separated metals. Sb(III), As(III), Cd, Cr, Cu, Fe, Pb, Mo, Ni, Ag, V, and Zn can then be determined simultaneously by ICP-AES. In an experiment designed to measure the coprecipitation efficiency, Sb(III), Cd and Ag were recovered at 70 to 75% of their original concentration. The remaining metals were recovered at 85 to 100% of their original concentrations, however. The range for the lower limits of determination for the metals after preconcentration is 0.1 to 3.0 ??g/l. The precision of the method was evaluated by replicate analyses of a Colorado creek water and two simulated water samples. The accuracy of the method was estimated using a water reference standard (SRM 1643a) certified by the U.S. National Bureau of Standards. In addition, the method was evaluated by analyzing groundwater samples collected near a porphyry copper deposit in Arizona and by analyzing meltwater from glacier-covered areas favorable for mineralization in south-central Alaska. The results for the ICP-AES analyses compared favorably with those obtained using the sequential technique of GFAAS on the acidified but unconcentrated water samples. ICP-AES analysis of trace-metal preconcentrates for hydrogeochemical surveys is more efficient than GFAAS because a

  13. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Progress report, January 1, 1990--December 31, 1992

    SciTech Connect

    Montaser, A.

    1992-09-01

    New high temperature plasmas and new sample introduction systems are explored for rapid elemental and isotopic analysis of gases, solutions, and solids using mass spectrometry and atomic emission spectrometry. Emphasis was placed on atmospheric pressure He inductively coupled plasmas (ICP) suitable for atomization, excitation, and ionization of elements; simulation and computer modeling of plasma sources with potential for use in spectrochemical analysis; spectroscopic imaging and diagnostic studies of high temperature plasmas, particularly He ICP discharges; and development of new, low-cost sample introduction systems, and examination of techniques for probing the aerosols over a wide range. Refs., 14 figs. (DLC)

  14. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Progress report, January 1, 1994--December 31, 1994

    SciTech Connect

    Montaser, A.

    1994-09-01

    This research follows a multifaceted approach, from theory to practice, to the investigation and development of novel helium plasmas, sample introduction systems, and diagnostic techniques for atomic and mass spectrometries. During the period January 1994 - December 1994, four major sets of challenging research programs were addressed that each included a number of discrete but complementary projects: (1) The first program is concerned with fundamental and analytical investigations of novel atmospheric-pressure helium inductively coupled plasmas (He ICPS) that are suitable for the atomization-excitation-ionization of elements, especially those possessing high excitation and ionization energies, for the purpose of enhancing sensitivity and selectivity of analytical measurements. (2) The second program includes simulation and computer modeling of He ICPS. The aim is to ease the hunt for new helium plasmas by predicting their structure and fundamental and analytical properties, without incurring the enormous cost for extensive experimental studies. (3) The third program involves spectroscopic imaging and diagnostic studies of plasma discharges to instantly visualize their prevailing structures, to quantify key fundamental properties, and to verify predictions by mathematical models. (4) The fourth program entails investigation of new, low-cost sample introduction systems that consume micro- to nanoliter quantity of sample solution in plasma spectrometries. A portion of this research involves development and applications of novel diagnostic techniques suitable for probing key fundamental properties of aerosol prior to and after injection into high-temperature plasmas. These efforts, still in progress, collectively offer promise of solving singularly difficult analytical problems that either exist now or are likely to arise in the future in the various fields of energy generation, environmental pollution, material science, biomedicine and nutrition.

  15. Organised surfactant assemblies in analytical atomic spectrometry

    NASA Astrophysics Data System (ADS)

    Sanz-Medel, Alfredo; Fernandez de la Campa, Maria del Rosario; Gonzalez, Elisa Blanco; Fernandez-Sanchez, Maria Luisa

    1999-02-01

    The use of surfactant-based organised assemblies in analytical atomic spectroscopy is extensively and critically reviewed along three main lines: first, the ability of organised media to enhance detection of atomic spectroscopic methods by favourable manipulation of physical and chemical properties of the sample solution second, the extension of separation mechanisms by resorting to organised media and third a discussion of synergistic combinations of liquid chromatography separations and atomic detectors via the use of vesicular mobile phases. Changes in physical properties of sample solutions aspirated in atomic spectrometry by addition of surfactants can be advantageously used in at least four different ways: (i) to improve nebulisation efficiency; (ii) to enhance wettability of solid surfaces used for atomisation; (iii) to improve compatibility between aqueous and organic phases; and (iv) to achieve good dispersion of small particles in "slurry" techniques. Controversial results and statements published so far are critically discussed. The ability of surfactant-based organised assemblies, such as micelles and vesicles, to organise reactants at the molecular level has also been applied to enhance the characteristics of chemical generation of volalite species of metals and semi-metals (e.g., hydride or ethylide generation of As, Pb, Cd, Se, Sn, and cold vapour Hg generation) used in atomic methods. Enhancements in efficiency/transport of volatile species, increases in the reaction kinetics, stabilisation of some unstable species and changes in the selectivity of the reactions by surfactants are dealt with. Non-chromatographic cloud-point separations to design pre-concentration procedures with subsequent metal determination by atomic methods are addressed along with chromatographic separations of expanded scope by addition of surfactants to the conventional aqueous mobile phases of reversed-phase high-performance liquid chromatography. Finally, the synergistic

  16. Atomic Absorption, Atomic Fluorescence, and Flame Emission Spectrometry.

    ERIC Educational Resources Information Center

    Horlick, Gary

    1984-01-01

    This review is presented in six sections. Sections focus on literature related to: (1) developments in instrumentation, measurement techniques, and procedures; (2) performance studies of flames and electrothermal atomizers; (3) applications of atomic absorption spectrometry; (4) analytical comparisons; (5) atomic fluorescence spectrometry; and (6)…

  17. Analytical evaluation of atomic form factors: Application to Rayleigh scattering

    SciTech Connect

    Safari, L.; Santos, J. P.; Amaro, P.; Jänkälä, K.; Fratini, F.

    2015-05-15

    Atomic form factors are widely used for the characterization of targets and specimens, from crystallography to biology. By using recent mathematical results, here we derive an analytical expression for the atomic form factor within the independent particle model constructed from nonrelativistic screened hydrogenic wave functions. The range of validity of this analytical expression is checked by comparing the analytically obtained form factors with the ones obtained within the Hartee-Fock method. As an example, we apply our analytical expression for the atomic form factor to evaluate the differential cross section for Rayleigh scattering off neutral atoms.

  18. Atomic absorption spectrometry with a flame emission source

    NASA Astrophysics Data System (ADS)

    Calloway, Clifton P.; Jones, Bradley T.

    1994-12-01

    An atomic absorption spectrometer with flame atomization and a flame emission light source is described. The light source is prepared by aspirating a solution containing a high concentration of analyte into the emission flame. Two different source flames (air/acetylene and nitrous oxide/acetylene) have been evaluated, with the N 2O flame providing better signal to noise ratios ( S/N) in most cases. Source S/N values as high as 5900 (Cr) have been observed. Experimental parameters have been optimized for nine test elements to give limits of detection obtained with this system that are in some cases as good as those obtained with the traditional hollow cathode lamp source; for example, Cu (4 ng/ml), Mn (3 ng/ml) and Ni (5 ng/ml). Linear dynamic ranges typically span 2-3 orders of magnitude. This system offers an inexpensive emission source with the ability to quickly change the setup to accommodate different analytes.

  19. A Thermo-Chemical Reactor for analytical atomic spectrometry

    NASA Astrophysics Data System (ADS)

    Gilmutdinov, A. Kh.; Nagulin, K. Yu.

    2009-01-01

    A novel atomization/vaporization system for analytical atomic spectrometry is developed. It consists of two electrically and thermally separated parts that can be heated separately. Unlike conventional electrothermal atomizers in which atomization occurs immediately above the vaporization site and at the same instant of time, the proposed system allows analyte atomization via an intermediate stage of fractional condensation as a two stage process: Vaporization → Condensation → Atomization. The condensation step is selective since vaporized matrix constituents are mainly non-condensable gases and leave the system by diffusion while analyte species are trapped on the cold surface of a condenser. This kind of sample distillation keeps all the advantages of traditional electrothermal atomization and allows significant reduction of matrix interferences. Integration into one design a vaporizer, condenser and atomizer gives much more flexibility for in situ sample treatment and thus the system is called a Thermo-Chemical Reactor (TCR). Details of the design, temperature measurements, vaporization-condensation-atomization mechanisms of various elements in variety of matrices are investigated in the TCR with spectral, temporal and spatial resolution. The ability of the TCR to significantly reduce interferences and to conduct sample pyrolysis at much higher temperatures as compared to conventional electrothermal atomizers is demonstrated. The analytical potential of the system is shown when atomic absorption determination of Cd and Pb in citrus leaves and milk powder without the use of any chemical modification.

  20. Analytical estimate for low-altitude ENA emissivity

    NASA Astrophysics Data System (ADS)

    Goldstein, J.; Bisikalo, D. V.; Shematovich, V. I.; Gérard, J.-C.; Søraas, F.; McComas, D. J.; Valek, P. W.; LLera, K.; Redfern, J.

    2016-02-01

    We formulate the first analytical model for energetic neutral atom (ENA) emissivity that partially corrects for the global viewing geometry dependence of low-altitude emissions (LAEs) observed by Two Wide-angle Imaging Neutral-atom Spectrometers (TWINS). The emissivity correction requires the pitch angle distribution (PAD) and geophysical location of low-altitude ENAs. To estimate PAD, we create an energy-dependent analytical model, based on a Monte Carlo simulation. We account for energy binning by integrating model PAD over each energy bin. We account for finite angular pixels by computing emissivity as an integral over the pitch angle range sampled by the pixel. We investigate location uncertainty in TWINS pixels by performing nine variations of the emissivity calculation. Using TWINS 2 ENA imaging data from 1131 to 1145 UT on 6 April 2010, we derive emissivity-corrected ion fluxes for two angular pixel sizes: 4° and 1°. To evaluate the method, we compare TWINS-derived ion fluxes to simultaneous in situ data from the National Oceanic and Atmospheric Administration (NOAA) 17 satellite. The TWINS-NOAA agreement for emissivity-corrected flux is improved by up to a factor of 7, compared to uncorrected flux. The highest 1° pixel fluxes are a factor of 2 higher than for 4° pixels, consistent with pixel-derived fluxes that are artificially low because subpixel structures are smoothed out, and indicating a possible slight advantage to oversampling the instrument-measured LAE signal. Both TWINS and NOAA ion fluxes decrease westward of 2000 magnetic local time. The TWINS-NOAA comparison indicates that the global ion precipitation oval comprises multiple smaller-scale (3-5° of latitude) structures.

  1. High-voltage spark atomic emission detector for gas chromatography

    NASA Technical Reports Server (NTRS)

    Calkin, C. L.; Koeplin, S. M.; Crouch, S. R.

    1982-01-01

    A dc-powered, double-gap, miniature nanosecond spark source for emission spectrochemical analysis of gas chromatographic effluents is described. The spark is formed between two thoriated tungsten electrodes by the discharge of a coaxial capacitor. The spark detector is coupled to the gas chromatograph by a heated transfer line. The gas chromatographic effluent is introduced into the heated spark chamber where atomization and excitation of the effluent occurs upon breakdown of the analytical gap. A microcomputer-controlled data acquisition system allows the implementation of time-resolution techniques to distinguish between the analyte emission and the background continuum produced by the spark discharge. Multiple sparks are computer averaged to improve the signal-to-noise ratio. The application of the spark detector for element-selective detection of metals and nonmetals is reported.

  2. Analytic Solution of a Two-Dimensional Hydrogen Atom

    NASA Astrophysics Data System (ADS)

    Yang, Xiao-Li.

    1990-03-01

    The two dimensional hydrogen atom problem is solved analytically in both the relativistic and non-relativistic cases. In the nonrelativistic case, exact formulae for energy eigenvalues and eigenfunctions for both the discrete and continuous parts of the spectrum, dipole matrix elements, DC Stark effect, single- and two-photon transition rate, fine and hyperfine structures are obtained. The binding energy of the ground state is found to be reduced by a factor of four from that of a three dimensional hydrogen atom. In the relativistic case, exact analytic expressions for discrete eigen energy and normalized eigen wave function are derived. It is shown that the solution to the Dirac equation is disjoint in the spin-coordinate space (four -component spinor) in contrast to the three dimensional counterpart. This surprising result is a consequence of the planar motion of the electron.

  3. ATOMIC AND MOLECULAR PHYSICS: Four-parameter analytical local model potential for atoms

    NASA Astrophysics Data System (ADS)

    Yu, Fei; Sun, Jiu-Xun; Tian, Rong-Gang; Yang, Wei

    2009-10-01

    Analytical local model potential for modeling the interaction in an atom reduces the computational effort in electronic structure calculations significantly. A new four-parameter analytical local model potential is proposed for atoms Li through Lr, and the values of four parameters are shell-independent and obtained by fitting the results of Xa method. At the same time, the energy eigenvalues, the radial wave functions and the total energies of electrons are obtained by solving the radial Schrödinger equation with a new form of potential function by Numerov's numerical method. The results show that our new form of potential function is suitable for high, medium and low Z atoms. A comparison among the new potential function and other analytical potential functions shows the greater flexibility and greater accuracy of the present new potential function.

  4. An analytical method for computing atomic contact areas in biomolecules.

    PubMed

    Mach, Paul; Koehl, Patrice

    2013-01-15

    We propose a new analytical method for detecting and computing contacts between atoms in biomolecules. It is based on the alpha shape theory and proceeds in three steps. First, we compute the weighted Delaunay triangulation of the union of spheres representing the molecule. In the second step, the Delaunay complex is filtered to derive the dual complex. Finally, contacts between spheres are collected. In this approach, two atoms i and j are defined to be in contact if their centers are connected by an edge in the dual complex. The contact areas between atom i and its neighbors are computed based on the caps formed by these neighbors on the surface of i; the total area of all these caps is partitioned according to their spherical Laguerre Voronoi diagram on the surface of i. This method is analytical and its implementation in a new program BallContact is fast and robust. We have used BallContact to study contacts in a database of 1551 high resolution protein structures. We show that with this new definition of atomic contacts, we generate realistic representations of the environments of atoms and residues within a protein. In particular, we establish the importance of nonpolar contact areas that complement the information represented by the accessible surface areas. This new method bears similarity to the tessellation methods used to quantify atomic volumes and contacts, with the advantage that it does not require the presence of explicit solvent molecules if the surface of the protein is to be considered. © 2012 Wiley Periodicals, Inc.

  5. Spontaneous emission of an atom in the presence of nanobodies

    SciTech Connect

    Klimov, Vasilii V; Ducloy, M; Letokhov, V S

    2001-07-31

    The effect of nanobodies, i.e., the bodies whose size is small compared to the emission wavelength, on spontaneous emission of an atom located near them is considered. The results of calculations performed within the framework of quantum and classical electrodynamics are presented both in analytic and graphical forms and can be readily used for planning experiments and analysis of experimental data. It is shown that nanobodies can be used to control efficiently the rate of spontaneous transitions. Thus, an excited atom located near a nanocylinder or a nanospheroid pole, whose transition dipole moment is directed normally to the nanobody surface, can decay with the rate that is tens and hundreds times higher than the decay rate in a free space. In the case of some (negative) dielectric constants, the decay rate can increase by a factor of 10{sup 5}-10{sup 6} and more. On the other hand, the decay of an excited atom whose transition dipole moment is directed tangentially to the nanobody surface substantially slows down. The probability of nonradiative decay of the excited state is shown to increase substantially in the presence of na-nobodies possessing losses. (review)

  6. Atomic line emission analyzer for hydrogen isotopes

    DOEpatents

    Kronberg, J.W.

    1993-03-30

    Apparatus for isotopic analysis of hydrogen comprises a low pressure chamber into which a sample of hydrogen is introduced and then exposed to an electrical discharge to excite the electrons of the hydrogen atoms to higher energy states and thereby cause the emission of light on the return to lower energy states, a Fresnel prism made at least in part of a material anomalously dispersive to the wavelengths of interest for dispersing the emitted light, and a photodiode array for receiving the dispersed light. The light emitted by the sample is filtered to pass only the desired wavelengths, such as one of the lines of the Balmer series for hydrogen, the wavelengths of which differ slightly from one isotope to another. The output of the photodiode array is processed to determine the relative amounts of each isotope present in the sample. Additionally, the sample itself may be recovered using a metal hydride.

  7. Atomic line emission analyzer for hydrogen isotopes

    DOEpatents

    Kronberg, James W.

    1993-01-01

    Apparatus for isotopic analysis of hydrogen comprises a low pressure chamber into which a sample of hydrogen is introduced and then exposed to an electrical discharge to excite the electrons of the hydrogen atoms to higher energy states and thereby cause the emission of light on the return to lower energy states, a Fresnel prism made at least in part of a material anomalously dispersive to the wavelengths of interest for dispersing the emitted light, and a photodiode array for receiving the dispersed light. The light emitted by the sample is filtered to pass only the desired wavelengths, such as one of the lines of the Balmer series for hydrogen, the wavelengths of which differ slightly from one isotope to another. The output of the photodiode array is processed to determine the relative amounts of each isotope present in the sample. Additionally, the sample itself may be recovered using a metal hydride.

  8. Atomic line emission analyzer for hydrogen isotopes

    DOEpatents

    Kronberg, J.W.

    1991-05-08

    Apparatus for isotopic analysis of hydrogen comprises a low pressure chamber into which a sample of hydrogen is introduced and then exposed to an electrical discharge to excite the electrons of the hydrogen atoms to higher energy states and thereby cause the emission of light on the return to lower energy states, a Fresnel prism made at least in part of a material anomalously dispersive to the wavelengths of interest for dispersing the emitted light, and a photodiode array for receiving the dispersed light. The light emitted by the sample is filtered to pass only the desired wavelengths, such as one of the lines of the Balmer series for hydrogen, the wavelengths of which differ slightly from one isotope to another. The output of the photodiode array is processed to determine the relative amounts of each isotope present in the sample. Additionally, the sample itself may be recovered using, a metal hydride.

  9. Study of atomic and molecular emission spectra of Sr by laser induced breakdown spectroscopy (LIBS).

    PubMed

    Bhatt, Chet R; Alfarraj, Bader; Ayyalasomayajula, Krishna K; Ghany, Charles; Yueh, Fang Y; Singh, Jagdish P

    2015-12-01

    Laser Induced Breakdown Spectroscopy (LIBS) is an ideal analytical technique for in situ analysis of elemental composition. We have performed a comparative study of the quantitative and qualitative analysis of atomic and molecular emission from LIBS spectra. In our experiments, a mixture of SrCl2 and Al2O3 in powder form was used as a sample. The atomic emission from Sr and molecular emission from SrCl and SrO observed in LIBS spectra were analyzed. The optimum laser energies, gate delays, and gate widths for selected atomic lines and molecular bands were determined from spectra recorded at various experimental parameters. These optimum experimental conditions were used to collect calibration data, and the calibration curves were used to predict the Sr concentration. Limits of detection (LODs) for selected atomic and molecular emission spectra were determined.

  10. ENVIRONMENTAL APPLICATION OF GAS CHROMATOGRAPHY/ATOMIC EMISSION DETECTION

    EPA Science Inventory

    A gas chromatography/atomic emission detector (GC/AED) system has been evaluated for its applicability to environmental analysis. Detection limits, elemental response factors, and regression analysis data were determined for 58 semivolatile environmental contaminants. Detection l...

  11. Spreadsheet-Based Program for Simulating Atomic Emission Spectra

    ERIC Educational Resources Information Center

    Flannigan, David J.

    2014-01-01

    A simple Excel spreadsheet-based program for simulating atomic emission spectra from the properties of neutral atoms (e.g., energies and statistical weights of the electronic states, electronic partition functions, transition probabilities, etc.) is described. The contents of the spreadsheet (i.e., input parameters, formulas for calculating…

  12. Indirect determination of cations by ion chromatography and anions by atomic emission spectroscopy

    SciTech Connect

    Ervin, A.M.; Panayappan, R.; Cooper, J.C.

    1988-11-01

    A method for the indirect determination of cations by Ion Chromatography (IC) and anions by Atomic Emission Spectroscopy (DCP) is described. The method allows for quantification of suspected impurities in aqueous systems where multiple analyses are desired. The described method is based on the selection of a precipitating agent for the desired analyte. In this study, silver(I) and barium(II) were analyzed indirectly by IC, and chloride and sulfate, by DCP.

  13. Stibine and bismuthine trapping in quartz tube atomizers for atomic absorption spectrometry — Method optimization and analytical applications

    NASA Astrophysics Data System (ADS)

    Kratzer, Jan; Dědina, Jiří

    2008-08-01

    The compact trap-and-atomizer device was employed to trap stibine and bismuthine, and subsequently to volatilize collected analyte and atomize it for atomic absorption spectrometric detection. The device is actually the multiple microflame quartz tube atomizer (multiatomizer) with inlet arm modified to serve as the trap and to accommodate the oxygen delivery capillary employed for burning out hydrogen during the trapping step. The optimization of Sb and Bi collection in the device is presented based on a study of the influence of relevant experimental parameters on preconcentration efficiency of both analytes. The parameters studied were: (1) trap temperature during trapping and (2) hydrogen flow rate and (3) trap temperature during volatilization and (4) the stability of the trapped analyte species. Under optimized conditions, the preconcentration efficiency was 100% for both analytes. The trap-and-atomizer device can be replaced by the simple conventional externally heated quartz tube atomizer without any trap as demonstrated on the ultratrace antimony determination in groundwater reference material and mineral water samples. The interference of other hydride forming elements on Bi in-situ collection in the conventional externally heated quartz tube atomizer was investigated.

  14. Effect of discharge parameters on emission yields in a radio-frequency glow-discharge atomic-emission source

    NASA Astrophysics Data System (ADS)

    Parker, Mark; Hartenstein, Matthew L.; Marcus, R. Kenneth

    1997-05-01

    A study is performed on a radio-frequency glow-discharge atomic-emission (rf-GD-AES) source to determine the factors effecting the emission yields for both metallic and nonconductive sample types. Specifically, these studies focus on determining how the operating parameters (power and pressure) influence emission yields. The results follow predicted patterns as determined by Langmuir probe diagnostic studies of a similar source. In particular, discharge gas pressure is the key operating parameter as slight changes in pressure may significantly affect the emission yield of the analyte species. RF power is less important and is shown to produce only relatively small changes in the emission yield over the ranges typically used in rf-GD analyses. These studies indicate that the quantitative analysis of layered materials, depth-profiling, may be adversely affected if the data collection scheme, i.e. the quantitative algorithm, requires changing the pressure during an analysis to keep the operating current and voltage constant. A direct relationship is shown to exist between the Ar (discharge gas) emission intensity and that of sputtered species for nonconductors. This observance is used to compensate for differences in emission intensities observed in the analysis of various thickness nonconductive samples. The sputtered element emission signals are corrected based on the emission intensity of an Ar (1) transition, implying that quantitative analysis of nonconductive samples is not severely limited by the availability of matrix matched standards.

  15. Atomic emission in the ultraviolet nightglow

    NASA Astrophysics Data System (ADS)

    Sharp, W. E.; Siskind, D. E.

    1989-12-01

    An observation of the ultraviolet nightglow between 2670 A and 3040 A was conducted over White Sands Missile Range on October 22, 1984, at 0020 hours LST during the Orionids meteor shower. A 1/4-meter UV spectrometer operating at 3.5 A resolution viewed the earth's limb at tangent heights between 90 km and 110 km for 120 seconds. By inverting the observed limb intensities, a total zenith intensity of 1.4 kR is inferred for the Herzberg I system. Excess emission above the Herzberg I (7,3) band at 2852 A is identified as the Mg I resonance line. The intensity ratio of the Herzberg I band system to the 2972 A line from O(1S) was less than that predicted from the accepted O(1S) branching ratio and acceptable ratios of Herzberg I to 5577 A emissions. Arguments supporting the identification of the Herzberg III band system are also advanced.

  16. Atomic emission in the ultraviolet nightglow

    SciTech Connect

    Sharp, W.E.; Siskind, D.E. )

    1989-12-01

    An observation of the ultraviolet nightglow between 2,670 {angstrom} and 3,040 {angstrom} was conducted over White Sands Missile Range on October 22, 1984, at 0020 hours LST during the Orionids meteor shower. A 1/4-meter uv spectrometer operating at 3.5 {angstrom} resolution viewed the Earth's limb at tangent heights between 90 km and 110 km for 120 seconds. By inverting the observed limb intensities, a total zenith intensity of 1.4 kR is inferred for the Herzberg I system. Excess emission above the Herzberg I (7,3) band at 2,852 {angstrom} is identified as the Mg I resonance line. The intensity ratio of the Herzberg I band system to the 2,972 {angstrom} line from O({sup 1}S) was less than that predicted from the accepted O({sup 1}S) branching ratio and acceptable ratios of Herzberg I to 5,577 {angstrom} emissions. Arguments supporting the identification of the Herzberg III band system are also advanced.

  17. Analytical study of ultrasound influence on the molten metals atomization

    NASA Astrophysics Data System (ADS)

    Antonnikova, A.; Arkhipov, V.; Boiko, V.; Basalaev, S.; Konovalenko, A.; Zolotorev, N.

    2016-04-01

    This paper focuses on the study of influence of ultrasound on liquid atomization using ejection nozzles. Two principles of influence of ultrasound on the atomization process such as a change of conditions on gas-liquid boundary during the generation of ultrasound oscillation in the gas and liquid jet (film) disintegration under the action of capillary forces in cases of generation of ultrasound oscillation in the liquid are considered. The optimal values of the ultrasound oscillation frequencies are calculated. Two constructions of the nozzles patented are proposed.

  18. EQUIB: Atomic level populations and line emissivities calculator

    NASA Astrophysics Data System (ADS)

    Howarth, I. D.; Adams, S.; Clegg, R. E. S.; Ruffle, D. P.; Liu, X.-W.; Pritchet, C. J.; Ercolano, B.

    2016-03-01

    The Fortran program EQUIB solves the statistical equilibrium equation for each ion and yields atomic level populations and line emissivities for given physical conditions, namely electron temperature and electron density, appropriate to the zones in an ionized nebula where the ions are expected to exist.

  19. SIMULTANEOUS DETERMINATION OF ORGANOTIN, ORGANOLEAD, AND ORGANOMERCURY COMPOUNDS IN ENVIRONMENTAL SAMPLES USING CAPILLARY GAS CHROMATOGRAPHY WITH ATOMIC EMISSION DETECTION

    EPA Science Inventory

    As part of a continuing evaluation of new analytical and sample preparation techniques conducted by the US Environmental Protection Agency (EPA), the use of capillary gas chromatography with atomic emission detection (GC-AED) for the simultaneous determination of organotin, organ...

  20. Sampling and analysis of particulate matter by glow discharge atomic emission and mass spectrometries.

    PubMed

    Marcus, R K; Dempster, M A; Gibeau, T E; Reynolds, E M

    1999-08-01

    The direct introduction of particulate matter into glow discharge atomic emission and mass spectrometry sources through a particle beam/momentum separator apparatus is described. Vacuum action through a narrow (0.0625 in. i.d.) stainless steel tube allows the introduction of discrete samples of NIST SRM 1648 urban particulate matter (UPM) and caffeine in powder form. Introduction of "ambient" airborne particulate matter is also possible. Particles passing through the aerodynamic momentum separator impinge on the heated (∼200-250 °C) inner surface of the glow discharge plasma volume and are flash-vaporized. The resultant atoms/molecules are subjected to excitation/ionization collisions within the low-pressure (0.5-5 Torr of He or Ar) plasma, producing characteristic photon emission and/or signature ionic species. In this way, atomic emission and mass spectrometry identification of particle constituents is possible. Basic design aspects of the apparatus are presented, and demonstrations of atomic emission detection of the constituents in the NIST SRM illustrate the general characteristics of the approach. Transient atomic emission signals are captured for the introduction of preweighed, discrete samples, with the integrated areas used to construct analytical response curves. Limits of detection using this relatively simple atomic emission system are on the order of tens of nanograms for sample masses of ∼50 μg. Mass spectrometric monitoring of introduced caffeine particles and a mixture of polycyclic aromatic hydrocarbons (PAHs) illustrates the ability of the glow discharge plasma to produce high-quality, library (electron impact) searchable mass spectra of molecular species while also yielding isotopic identification of elemental components of the UPM. Limits of detection for Fe in the NIST SRM are on the order of 175 ng of material, equivalent to ∼7 ng of analyte Fe. It is believed that the small size, low power consumption, ease of operation, and multimode

  1. Investigations on Freon-assisted atomization of refractory analytes (Cr, Mo, Ti, V) in multielement electrothermal atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Heinrich, Hans-Joachim; Matschat, Ralf

    2007-08-01

    Premixed 1% Freon in argon inner gas of various composition (CCl 2F 2, CHClF 2, CHF 3) was applied to graphite furnace atomizer to minimize unfavorable effects of carbide formation, such as signal tailing and memory effects in the simultaneous determination of Cr, Mo, Ti and V refractory analytes by electrothermal atomic absorption spectrometry using a multielement atomic absorption spectrometer. The effect of these gaseous additives was investigated when applied separately in atomization, pyrolysis and clean-out steps. The halogenation effects were analytically useful only under the precondition of using Ar-H 2 outer gas to the furnace to all heating steps, and also using this gas in the pre-atomization (drying, pyrolysis) steps. Optimum analytical performance was obtained when mixtures of 1% Freon in argon were applied just before and during the atomization step at a flow rate of 50 mL min - 1 and 2% hydrogen was used as purge gas. Using optimum conditions, signal tailings and carry-over contamination were reduced effectively and good precision (relative standard deviation below 1%) could be attained. Applying 1% CHClF 2 and an atomization temperature of 2550 °C, the characteristic masses obtained for simple aqueous solutions were 8.8 pg for Cr, 17 pg for Mo, 160 pg for Ti, and 74 pg for V. The limits of detection were 0.05, 0.2, 2.3 and 0.5 μg L - 1 for Cr, Mo, Ti and V, respectively. The developed method was applied to the analysis of digests of advanced ceramics. The accuracy of the procedure was confirmed by analyzing the certified reference material ERM-ED 102 (Boron Carbide Powder) and a silicon nitride powder distributed in the inter-laboratory comparison CCQM-P74.

  2. Matrix-Assisted Plasma Atomization Emission Spectrometry for Surface Sampling Elemental Analysis

    PubMed Central

    Yuan, Xin; Zhan, Xuefang; Li, Xuemei; Zhao, Zhongjun; Duan, Yixiang

    2016-01-01

    An innovative technology has been developed involving a simple and sensitive optical spectrometric method termed matrix-assisted plasma atomization emission spectrometry (MAPAES) for surface sampling elemental analysis using a piece of filter paper (FP) for sample introduction. MAPAES was carried out by direct interaction of the plasma tail plume with the matrix surface. The FP absorbs energy from the plasma source and releases combustion heating to the analytes originally present on its surface, thus to promote the atomization and excitation process. The matrix-assisted plasma atomization excitation phenomenon was observed for multiple elements. The FP matrix served as the partial energy producer and also the sample substrate to adsorb sample solution. Qualitative and quantitative determinations of metal ions were achieved by atomic emission measurements for elements Ba, Cu, Eu, In, Mn, Ni, Rh and Y. The detection limits were down to pg level with linear correlation coefficients better than 0.99. The proposed MAPAES provides a new way for atomic spectrometry which offers advantages of fast analysis speed, little sample consumption, less sample pretreatment, small size, and cost-effective. PMID:26762972

  3. Matrix-Assisted Plasma Atomization Emission Spectrometry for Surface Sampling Elemental Analysis

    NASA Astrophysics Data System (ADS)

    Yuan, Xin; Zhan, Xuefang; Li, Xuemei; Zhao, Zhongjun; Duan, Yixiang

    2016-01-01

    An innovative technology has been developed involving a simple and sensitive optical spectrometric method termed matrix-assisted plasma atomization emission spectrometry (MAPAES) for surface sampling elemental analysis using a piece of filter paper (FP) for sample introduction. MAPAES was carried out by direct interaction of the plasma tail plume with the matrix surface. The FP absorbs energy from the plasma source and releases combustion heating to the analytes originally present on its surface, thus to promote the atomization and excitation process. The matrix-assisted plasma atomization excitation phenomenon was observed for multiple elements. The FP matrix served as the partial energy producer and also the sample substrate to adsorb sample solution. Qualitative and quantitative determinations of metal ions were achieved by atomic emission measurements for elements Ba, Cu, Eu, In, Mn, Ni, Rh and Y. The detection limits were down to pg level with linear correlation coefficients better than 0.99. The proposed MAPAES provides a new way for atomic spectrometry which offers advantages of fast analysis speed, little sample consumption, less sample pretreatment, small size, and cost-effective.

  4. Matrix-Assisted Plasma Atomization Emission Spectrometry for Surface Sampling Elemental Analysis.

    PubMed

    Yuan, Xin; Zhan, Xuefang; Li, Xuemei; Zhao, Zhongjun; Duan, Yixiang

    2016-01-01

    An innovative technology has been developed involving a simple and sensitive optical spectrometric method termed matrix-assisted plasma atomization emission spectrometry (MAPAES) for surface sampling elemental analysis using a piece of filter paper (FP) for sample introduction. MAPAES was carried out by direct interaction of the plasma tail plume with the matrix surface. The FP absorbs energy from the plasma source and releases combustion heating to the analytes originally present on its surface, thus to promote the atomization and excitation process. The matrix-assisted plasma atomization excitation phenomenon was observed for multiple elements. The FP matrix served as the partial energy producer and also the sample substrate to adsorb sample solution. Qualitative and quantitative determinations of metal ions were achieved by atomic emission measurements for elements Ba, Cu, Eu, In, Mn, Ni, Rh and Y. The detection limits were down to pg level with linear correlation coefficients better than 0.99. The proposed MAPAES provides a new way for atomic spectrometry which offers advantages of fast analysis speed, little sample consumption, less sample pretreatment, small size, and cost-effective. PMID:26762972

  5. Far ultraviolet atomic and molecular nitrogen emissions in the dayglow

    NASA Technical Reports Server (NTRS)

    Takacs, P. Z.; Feldman, P. D.

    1977-01-01

    A scanning spectrophotometer was used to observe the far ultraviolet day airglow between 1130 and 1520 A at 4.4-A spectral resolution. Fourteen bands of the N2 Lyman-Birge-Hopfield (LBH) system are clearly resolved and suggest a total LBH system zenith column emission rate of 3810 plus or minus 520 R extrapolated to the subsolar point. A photoelectron flux model (based on recent photoelectron flux measurements and the observed LBH altitude profile) is used to derive the direct and dissociative excitation contributions to the atomic nitrogen emissions. The calculated atomic nitrogen density agrees with other measurements, although it is an order of magnitude greater than previous photochemical model results.

  6. Atomic Auger Doppler effects upon emission of fast photoelectrons.

    PubMed

    Simon, Marc; Püttner, Ralph; Marchenko, Tatiana; Guillemin, Renaud; Kushawaha, Rajesh K; Journel, Loïc; Goldsztejn, Gildas; Piancastelli, Maria Novella; Ablett, James M; Rueff, Jean-Pascal; Céolin, Denis

    2014-01-01

    Studies of photoemission processes induced by hard X-rays including production of energetic electrons have become feasible due to recent substantial improvement of instrumentation. Novel dynamical phenomena have become possible to investigate in this new regime. Here we show a significant change in Auger emission following 1s photoionization of neon, which we attribute to the recoil of the Ne ion induced by the emission of a fast photoelectron. Because of the preferential motion of the ionized Ne atoms along two opposite directions, an Auger Doppler shift is revealed, which manifests itself as a gradual broadening and doubling of the Auger spectral features. This Auger Doppler effect should be a general phenomenon in high-energy photoemission of both isolated atoms and molecules, which will have to be taken into account in studies of other recoil effects such as vibrational or rotational recoil in molecules, and may also have consequences in measurements in solids. PMID:24906107

  7. Infrared [Fe II] Emission Lines from Radiative Atomic Shocks

    NASA Astrophysics Data System (ADS)

    Koo, Bon-Chul; Raymond, John C.; Kim, Hyun-Jeong

    2016-06-01

    [Fe II] emission lines are prominent in the infrared (IR) and important as diagnostic tools for radiative atomic shocks. We investigate the emission characteristics of [Fe II] lines using a shock code developed by te{raymond1979} with updated atomic parameters. We first review general characteristics of the IR [Fe II] emission lines from shocked gas, and derive their fluxes as a function of shock speed and ambient density. We have compiled available IR [Fe II] line observations of interstellar shocks and compare them to the ratios predicted from our model. The sample includes both young and old supernova remnants in the Galaxy and the Large Magellanic Cloud and several Herbig-Haro objects. We find that the observed ratios of the IR [Fe II] lines generally fall on our grid of shock models, but the ratios of some mid-IR lines, e.g., fethreefive/fetwofive, fefive/fetwofive, and fefive/feoneseven, are significantly offset from our model grid. We discuss possible explanations and conclude that while uncertainties in the shock modeling and the observations certainly exist, the uncertainty in atomic rates appears to be the major source of discrepancy.

  8. The Kalman filter approach to inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Van Veen, E. H.; Bosch, S.; De Loos-Vollebregt, M. T. C.

    1994-07-01

    This article is an electronic publication in Spectrochimica Acta Electronica (SAE), the electronic section of Spectrochimica Acta Part B (SAB). The hardcopy text, comprising the main article and two appendices, is accompanied by a disk containing the compiled program, a reference manual and data files. The work deals with data handling in inductively coupled plasma atomic emission spectrometry (ICP-AES). With this technique, the analyte signal is superimposed on a background signal. When separating the signals by manual or automated three-point background correction, there are many instances in which the data reduction fails. Based on scans recorded in a fast-scanning mode and on a library of pure-component scans, the Kaiman filter approach models the emission in the spectral window (about 100 pm) of the analyte and mathematically solves the problem of background correction. By using a criterion-based algorithm to correct for optical instability, the uncertainty in the determination of the interferent line signal is eliminated. Therefore, the present filter implementation yields more accurate and precise results, especially in the case of line overlap. The Kalman filter Approach to Atomic Spectrometry (KAAS) software automatically processes Perkin-Elmer Plasma 1000/2000 text files, but can also handle ASCII data files. Practical and comprehensive examples are given to evoke the "Kalman filter feeling" in the crucial step of creating the emission model.

  9. ATOMIC AND MOLECULAR PHYSICS: Spontaneous Emission of a Polarized Atom in a Medium Between Two Parallel Mirrors

    NASA Astrophysics Data System (ADS)

    Wang, De-Hua; Huang, Kai-Yun; Xu, Qiang

    2010-01-01

    Using the photon closed orbit theory, the spontaneous emission rate of a polarized atom in a medium between two parallel mirrors is derived and calculated. It is found that the spontaneous emission rate of a polarized atom between the mirrors is related to the atomic position and the polarization direction. The results show that in the vicinity of the mirror, the variation of the spontaneous emission rate depends crucially on the atomic polarization direction. With the increase of the polarization angle, the oscillation in the spontaneous emission rate becomes decreased. For the polarization direction parallel to the mirror plane, the oscillation is the greatest; while for the perpendicular polarization direction, the oscillation is nearly vanished. The agreement between our result and the quantum electrodynamics result suggests the correctness of our calculation. This study further verifies that the atomic spontaneous emission process can be effectively controlled by changing the polarization orientation of the atom.

  10. 40 CFR 87.64 - Sampling and analytical procedures for measuring gaseous exhaust emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Sampling and analytical procedures for measuring gaseous exhaust emissions. 87.64 Section 87.64 Protection of Environment ENVIRONMENTAL PROTECTION....64 Sampling and analytical procedures for measuring gaseous exhaust emissions. (a) The system...

  11. Electron impact induced light emission from zinc atoms

    NASA Astrophysics Data System (ADS)

    Cvejanovic, Danica

    2009-10-01

    Experimental studies of electron impact excitation of zinc atom are rare, primarily due to experimental difficulties. However, zinc is an interesting target because of possible applications in light sources. Also, due to its position in periodic table, zinc is an interesting case for the fundamental understanding of momentum couplings and the role of electron correlations in complex metal atoms. Recent experimental investigations have indicated the existence of highly correlated scattering mechanisms via formation of negative ion resonances and Post Collision Interaction (PCI) in the decay of autoionizing states. These can significantly modify energy dependence of the emission cross sections at low impact energies and the studies of photon emission offer a sensitive way to investigate electron correlations. Specifically, in the lowest autoionizing region of zinc, i.e. between 10 and 15 eV, both the cross sections and polarization of emitted light are affected by the formation of short lived negative ions and PCI effects. These are associated with excitation of one of the sub-valence 3d electrons and complex correlations between inner 3d and outer excited electrons in the target and also with the slow electron released into continuum, need to be included in modeling. Also the scattering of the spin polarized electrons has shown significant spin effects when excitation proceeds via negative ion resonances. Emission cross sections and comparison with theory would be discussed at the conference.

  12. Analytic description of atomic interaction at ultracold temperatures: The case of a single channel

    SciTech Connect

    Gao Bo

    2009-07-15

    We present analytic descriptions of atomic interaction at ultracold temperatures using both single-channel and multichannel quantum-defect theories. In the case of a single channel, addressed in this paper, the expansion of Gao [Phys. Rev. A 58, 4222 (1998)] is generalized to higher orders for angular momentum l{>=}2 to give a more complete description of ultracold scattering, including an analytic description of ultracold shape resonances of arbitrary l. We also introduce a generalized scattering length that is well defined and useful for all partial waves to replace the traditional definition that fails for l{>=}2 due to the long-range van der Waals interaction. The results are used in a companion paper to derive analytic descriptions of atomic interaction around a magnetic Feshbach resonance of arbitrary angular momentum l.

  13. Energetic neutral atom emissions from Titan interaction with Saturn's magnetosphere.

    PubMed

    Mitchell, D G; Brandt, P C; Roelof, E C; Dandouras, J; Krimigis, S M; Mauk, B H

    2005-05-13

    The Cassini Magnetospheric Imaging Instrument (MIMI) observed the interaction of Saturn's largest moon, Titan, with Saturn's magnetosphere during two close flybys of Titan on 26 October and 13 December 2004. The MIMI Ion and Neutral Camera (INCA) continuously imaged the energetic neutral atoms (ENAs) generated by charge exchange reactions between the energetic, singly ionized trapped magnetospheric ions and the outer atmosphere, or exosphere, of Titan. The images reveal a halo of variable ENA emission about Titan's nearly collisionless outer atmosphere that fades at larger distances as the exospheric density decays exponentially. The altitude of the emissions varies, and they are not symmetrical about the moon, reflecting the complexity of the interactions between Titan's upper atmosphere and Saturn's space environment.

  14. 40 CFR 87.82 - Sampling and analytical procedures for measuring smoke exhaust emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... measuring smoke exhaust emissions. 87.82 Section 87.82 Protection of Environment ENVIRONMENTAL PROTECTION... Test Procedures for Engine Smoke Emissions (Aircraft Gas Turbine Engines) § 87.82 Sampling and analytical procedures for measuring smoke exhaust emissions. The system and procedures for sampling...

  15. 40 CFR 87.82 - Sampling and analytical procedures for measuring smoke exhaust emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... measuring smoke exhaust emissions. 87.82 Section 87.82 Protection of Environment ENVIRONMENTAL PROTECTION... Test Procedures for Engine Smoke Emissions (Aircraft Gas Turbine Engines) § 87.82 Sampling and analytical procedures for measuring smoke exhaust emissions. The system and procedures for sampling...

  16. 14 CFR 34.64 - Sampling and analytical procedures for measuring gaseous exhaust emissions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... ADMINISTRATION, DEPARTMENT OF TRANSPORTATION AIRCRAFT FUEL VENTING AND EXHAUST EMISSION REQUIREMENTS FOR TURBINE ENGINE POWERED AIRPLANES Test Procedures for Engine Exhaust Gaseous Emissions (Aircraft and Aircraft Gas Turbine Engines) § 34.64 Sampling and analytical procedures for measuring gaseous exhaust emissions....

  17. Analytical solutions for the dynamics of two trapped interacting ultracold atoms

    SciTech Connect

    Idziaszek, Zbigniew; Calarco, Tommaso

    2006-08-15

    We discuss exact solutions of the Schroedinger equation for the system of two ultracold atoms confined in an axially symmetric harmonic potential. We investigate different geometries of the trapping potential, in particular we study the properties of eigenenergies and eigenfunctions for quasi-one-dimensional and quasi-two-dimensional traps. We show that the quasi-one-dimensional and the quasi-two-dimensional regimes for two atoms can be already realized in the traps with moderately large (or small) ratios of the trapping frequencies in the axial and the transverse directions. Finally, we apply our theory to Feshbach resonances for trapped atoms. Introducing in our description an energy-dependent scattering length we calculate analytically the eigenenergies for two trapped atoms in the presence of a Feshbach resonance.

  18. Laser excited analytical atomic and ionic fluorescence in flames, furnaces and inductively coupled plasmas—II. Fluorescence characteristics and detection limits for fourteen elements

    NASA Astrophysics Data System (ADS)

    Human, H. G. C.; Omenetto, N.; Cavalli, P.; Rossi, G.

    An account is given of the analytical characteristics of the elements Al, B, Ba, Ga, Mo, Pb, Si, Sn, Ti, Tl, V, Y, Zr and U in atomic and ionic fluorescence spectrometry using an excimer (XeCl) pumped pulsed dye laser as excitation source. The inductively coupled argon plasma was mainly used as atom/ion reservoir. The detection limits were found to be in the range 0.4-20 ng ml -1, improving "standard" tabulated ICP emission values by factors between 1 and 66. The separated air-acetylene flame and the carbon rod were also used as atom reservoir for a few volatile elements, the practical detection limit for lead with the latter being 6 × 10 -15g. The advantages and disadvantages of such an analytical system are discussed, one of the main advantages being certainly the high spectral selectivity of the technique.

  19. Three-dimensional time-dependent computer modeling of the electrothermal atomizers for analytical spectrometry

    NASA Astrophysics Data System (ADS)

    Tsivilskiy, I. V.; Nagulin, K. Yu.; Gilmutdinov, A. Kh.

    2016-02-01

    A full three-dimensional nonstationary numerical model of graphite electrothermal atomizers of various types is developed. The model is based on solution of a heat equation within solid walls of the atomizer with a radiative heat transfer and numerical solution of a full set of Navier-Stokes equations with an energy equation for a gas. Governing equations for the behavior of a discrete phase, i.e., atomic particles suspended in a gas (including gas-phase processes of evaporation and condensation), are derived from the formal equations molecular kinetics by numerical solution of the Hertz-Langmuir equation. The following atomizers test the model: a Varian standard heated electrothermal vaporizer (ETV), a Perkin Elmer standard THGA transversely heated graphite tube with integrated platform (THGA), and the original double-stage tube-helix atomizer (DSTHA). The experimental verification of computer calculations is carried out by a method of shadow spectral visualization of the spatial distributions of atomic and molecular vapors in an analytical space of an atomizer.

  20. Atomic emission detection for gas chromatographic analysis of nitrogen-containing herbicides in water.

    PubMed

    Olson, N L; Carrell, R; Cummings, R; Rieck, R; Reimer, S

    1995-01-01

    A gas chromatography-atomic emission detection (GC-AED) system was used to analyze nitrogen-containing herbicides. Two methods of sample preparation were used to demonstrate the system's applicability. Method 1 was U.S. Environmental Protection Agency (EPA) Method 507. Method 2 was a modification of EPA Method 507 using larger sample volumes and smaller extract volumes to yield compound detection levels 30 times lower than detection levels from method 1. Analysis of replicate reagent water spikes with method 1 gave analyte recoveries ranging from 82 to 107%, with standard deviations of recovery of not more than 6.7%. Method 2 gave recoveries ranging from 50 to 112%, with a standard deviation of recovery of not more than 33%. A loss in recovery and precision with method 2 compared with method 1 was attributed to loss of more volatile analytes during extract concentration. Selectivity was demonstrated with solvent spiked with fuel oil and atrazine. Response factors generated with the GC-AED system showed compound-independent elemental linearity for analytes. Relative standard deviations of not more than 5.34% were obtained for 3 elements tested: nitrogen, sulphur, and chlorine. An elemental calibration mixture was prepared to validate traditional methods of quantitation. Samples were analyzed for nitrogen-containing herbicides, which were quantitated with both an analyte calibration and an elemental calibration, and results were compared.

  1. Continuous Liquid-Sample Introduction for Bunsen Burner Atomic Emission Spectrometry.

    ERIC Educational Resources Information Center

    Smith, Gregory D.; And Others

    1995-01-01

    Describes a laboratory-constructed atomic emission spectrometer with modular instrumentation components and a simple Bunsen burner atomizer with continuous sample introduction. A schematic diagram and sample data are provided. (DDR)

  2. Microplasma-based atomic emission detectors for gas chromatography.

    PubMed

    Miclea, M; Okruss, M; Kunze, K; Ahlman, N; Franzke, J

    2007-08-01

    This paper is an update on the development of microplasmas as detectors for gas chromatography. Direct current (dc), alternating current (ac), and radio frequency (rf) microplasmas developed in recent years will be described with their significant analytical results, which mostly concern the detection of halogens and sulfur. New results will be added which employ a microhollow cathode discharge (MHCD) as excitation source. Emphasis will be given to this microplasma which has already been implemented as an element-selective detector for emission spectrometry and as ionization source for mass spectrometry. The possibility to use it as a multielement-selective detector for gas chromatography will be presented. A discussion of the published detection limits of all these microplasmas is given.

  3. Fully analytical integration over the 3D volume bounded by the β sphere in topological atoms.

    PubMed

    Popelier, Paul L A

    2011-11-17

    Atomic properties of a topological atom are obtained by 3D integration over the volume of its atomic basin. Algorithms that compute atomic properties typically integrate over two subspaces: the volume bounded by the so-called β sphere, which is centered at the nucleus and completely contained within the atomic basin, and the volume of the remaining part of the basin. Here we show how the usual quadrature over the β sphere volume can be replaced by a fully analytical 3D integration leading to the atomic charge (monopole moment) for s, p, and d functions. Spherical tensor multipole moments have also been implemented and tested up to hexadecupole for s functions only, and up to quadrupole for s and p functions. The new algorithm is illustrated by operating on capped glycine (HF/6-31G, 35 molecular orbitals (MOs), 322 Gaussian primitives, 19 nuclei), the protein crambin (HF/3-21G, 1260 MOs, 5922 primitives and 642 nuclei), and tin (Z = 50) in Sn(2)(CH(3))(2) (B3LYP/cc-pVTZ and LANL2DZ, 59 MOs, 1352 primitives).

  4. Two-dimensional sub-half-wavelength atom localization via controlled spontaneous emission.

    PubMed

    Wan, Ren-Gang; Zhang, Tong-Yi

    2011-12-01

    We propose a scheme for two-dimensional (2D) atom localization based on the controlled spontaneous emission, in which the atom interacts with two orthogonal standing-wave fields. Due to the spatially dependent atom-field interaction, the position probability distribution of the atom can be directly determined by measuring the resulting spontaneously emission spectrum. The phase sensitive property of the atomic system leads to quenching of the spontaneous emission in some regions of the standing-waves, which significantly reduces the uncertainty in the position measurement of the atom. We find that the frequency measurement of the emitted light localizes the atom in half-wavelength domain. Especially the probability of finding the atom at a particular position can reach 100% when a photon with certain frequency is detected. By increasing the Rabi frequencies of the driving fields, such 2D sub-half-wavelength atom localization can acquire high spatial resolution.

  5. Analytical transition-matrix treatment of electric multipole polarizabilities of hydrogen-like atoms

    SciTech Connect

    Kharchenko, V.F.

    2015-04-15

    The direct transition-matrix approach to the description of the electric polarization of the quantum bound system of particles is used to determine the electric multipole polarizabilities of the hydrogen-like atoms. It is shown that in the case of the bound system formed by the Coulomb interaction the corresponding inhomogeneous integral equation determining an off-shell scattering function, which consistently describes virtual multiple scattering, can be solved exactly analytically for all electric multipole polarizabilities. Our method allows to reproduce the known Dalgarno–Lewis formula for electric multipole polarizabilities of the hydrogen atom in the ground state and can also be applied to determine the polarizability of the atom in excited bound states. - Highlights: • A new description for electric polarization of hydrogen-like atoms. • Expression for multipole polarizabilities in terms of off-shell scattering functions. • Derivation of integral equation determining the off-shell scattering function. • Rigorous analytic solving the integral equations both for ground and excited states. • Study of contributions of virtual multiple scattering to electric polarizabilities.

  6. Deriving Coarse-Grained Charges from All-Atom Systems: An Analytic Solution.

    PubMed

    McCullagh, Peter; Lake, Peter T; McCullagh, Martin

    2016-09-13

    An analytic method to assign optimal coarse-grained charges based on electrostatic potential matching is presented. This solution is the infinite size and density limit of grid-integration charge-fitting and is computationally more efficient by several orders of magnitude. The solution is also minimized with respect to coarse-grained positions which proves to be an extremely important step in reproducing the all-atom electrostatic potential. The joint optimal-charge optimal-position coarse-graining procedure is applied to a number of aggregating proteins using single-site per amino acid resolution. These models provide a good estimate of both the vacuum and Debye-Hückel screened all-atom electrostatic potentials in the vicinity and in the far-field of the protein. Additionally, these coarse-grained models are shown to approximate the all-atom dimerization electrostatic potential energy of 10 aggregating proteins with good accuracy.

  7. The use of analytical surface tools in the fundamental study of wear. [atomic nature of wear

    NASA Technical Reports Server (NTRS)

    Buckley, D. H.

    1977-01-01

    Various techniques and surface tools available for the study of the atomic nature of the wear of materials are reviewed These include chemical etching, x-ray diffraction, electron diffraction, scanning electron microscopy, low-energy electron diffraction, Auger emission spectroscopy analysis, electron spectroscopy for chemical analysis, field ion microscopy, and the atom probe. Properties of the surface and wear surface regions which affect wear, such as surface energy, crystal structure, crystallographic orientation, mode of dislocation behavior, and cohesive binding, are discussed. A number of mechanisms involved in the generation of wear particles are identified with the aid of the aforementioned tools.

  8. Directed spontaneous emission from an extended ensemble of N atoms: timing is everything.

    PubMed

    Scully, Marlan O; Fry, Edward S; Ooi, C H Raymond; Wódkiewicz, Krzysztof

    2006-01-13

    A collection of static atoms is fixed in a crystal at a low temperature and prepared by a pulse of incident radiation of wave vector . The atoms are well described by an entangled Dicke-like state, in which each atom carries a characteristic phase factor exp(ik0.r(j)), where is the atomic position in the crystal. It is shown that a single photon absorbed by the N atoms will be followed by spontaneous emission in the same direction. Furthermore, phase matched emission is found when one photon is absorbed by N atoms followed by two-photon down-conversion.

  9. 40 CFR 87.82 - Sampling and analytical procedures for measuring smoke exhaust emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... measuring smoke exhaust emissions. 87.82 Section 87.82 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) Definitions. Test Procedures for Engine Smoke Emissions (Aircraft Gas Turbine Engines) § 87.82 Sampling and analytical procedures for measuring smoke...

  10. 14 CFR 34.64 - Sampling and analytical procedures for measuring gaseous exhaust emissions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. This document can be obtained from the... ADMINISTRATION, DEPARTMENT OF TRANSPORTATION AIRCRAFT FUEL VENTING AND EXHAUST EMISSION REQUIREMENTS FOR TURBINE... Turbine Engines) § 34.64 Sampling and analytical procedures for measuring gaseous exhaust emissions....

  11. 14 CFR 34.64 - Sampling and analytical procedures for measuring gaseous exhaust emissions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. This document can be obtained from the... ADMINISTRATION, DEPARTMENT OF TRANSPORTATION AIRCRAFT FUEL VENTING AND EXHAUST EMISSION REQUIREMENTS FOR TURBINE... Turbine Engines) § 34.64 Sampling and analytical procedures for measuring gaseous exhaust emissions....

  12. Methods for detecting and correcting inaccurate results in inductively coupled plasma-atomic emission spectrometry

    DOEpatents

    Chan, George C. Y.; Hieftje, Gary M.

    2010-08-03

    A method for detecting and correcting inaccurate results in inductively coupled plasma-atomic emission spectrometry (ICP-AES). ICP-AES analysis is performed across a plurality of selected locations in the plasma on an unknown sample, collecting the light intensity at one or more selected wavelengths of one or more sought-for analytes, creating a first dataset. The first dataset is then calibrated with a calibration dataset creating a calibrated first dataset curve. If the calibrated first dataset curve has a variability along the location within the plasma for a selected wavelength, errors are present. Plasma-related errors are then corrected by diluting the unknown sample and performing the same ICP-AES analysis on the diluted unknown sample creating a calibrated second dataset curve (accounting for the dilution) for the one or more sought-for analytes. The cross-over point of the calibrated dataset curves yields the corrected value (free from plasma related errors) for each sought-for analyte.

  13. Spectroscopic Characteristic and Analytical Capability of Ar-N₂ Inductively Coupled Plasma in Axially Viewing Optical Emission Spectrometry.

    PubMed

    Ohata, Masaki

    2016-01-01

    The spectroscopic characteristics and analytical capability of argon-nitrogen (Ar-N2) inductively coupled plasma (ICP) in axially viewing optical emission spectrometry (OES) were examined and figures of merit were determined in the present study. The spectroscopic characteristics such as the emission intensity profile and the excitation temperature observed from the analytical zone of Ar-N2 ICP in axially viewing ICPOES, in order to elucidate the enhancement of the emission intensity of elements obtained in our previous study, were evaluated and compared to those of the standard ICP. The background and emission intensities of elements as well as their excitation behavior for both atom and ion lines were also examined. As results, a narrower emission intensity profile and an increased excitation temperature as well as enhancements for both background and emission intensities of elements, which could be due to the ICP shrunken as well as the enhancement of the interaction between the central channel of the ICP and samples introduced, were observed for Ar-N2 ICP in axially viewing OES. In addition, the elements with relatively higher excitation and ionization energies such as As, Bi, Cd, Ni, P, and Zn revealed larger enhancements of the emission intensities as well as improved limits of detection (LODs), which were also attributed to the enhanced interaction between Ar-N2 ICP and the samples. Since the Ar-N2 ICP could be obtained easily only by the addition of a small amount of N2 gas to the Ar plasma gas of the standard ICP and no optimization on the alignment between Ar-N2 ICP and the spectrometer in commercially available ICPOES instruments was needed, it could be utilized as simple and optional excitation and ionization sources in axially viewing ICPOES. PMID:26860569

  14. Multi-analyte calibration curve for high-performance liquid chromatography with an inductively coupled plasma carbon emission detector.

    PubMed

    Peters, Heather L; Hou, Xiandeng; Jones, Bradley T

    2003-09-01

    A liquid chromatography system with an inductively coupled plasma detector is used to prepare a single calibration curve that is useful for multiple analytes. The detector monitors the atomic emission from carbon at 193.09 nm. Hence, the analytes need not exhibit appreciable molar absorptivity or native fluorescence. Since the carbon signal is independent of molecular structure, the sensitivities for different compounds are similar as long as nebulization efficiencies are comparable. In fact, with a suitable internal standard, no calibration curve is necessary. The capability of the system is demonstrated with a test mixture of nine amino acids separated with a C30 reversed-phase column and a 20 mM phosphate buffered mobile phase. The system provides a detection limit of 30 ng carbon. A multi-analyte calibration curve is prepared with 135 distinct measurements: each of nine analytes, at five different concentrations, repeated in triplicate. The average relative standard deviation for 27 measurements of different amino acids at a given concentration is 2.5%. Clearly, a single analyte will suffice for the calibration of all nine test compounds. Similarly, the internal standard method provides an average percent error of 2.0% for the determination of 45 different amino acid concentrations using only a single replicate for each sample.

  15. Analytic expressions for the proximity energy, the fusion process and the α emission

    NASA Astrophysics Data System (ADS)

    Moustabchir, R.; Royer, G.

    2001-02-01

    The entrance and exit channels through quasimolecular shapes are compatible with the experimental data on fusion, light nucleus and α emissions when the proximity energy is taken into account. Analytic expressions allowing to determine rapidly this proximity energy are presented as well as formulas for the fusion barrier heights and radii and for the α emission barriers. Predictions for half-lives of exotic α emissions are proposed.

  16. Multielement analysis of geologic materials by inductively coupled plasma-atomic emission spectroscopy

    SciTech Connect

    Christensen, O.D.; Kroneman, R.L.; Capuano, R.M.

    1980-03-01

    Atomic emission spectroscopy using an inductively coupled plasma (ICP) source permits the rapid acquisition of multielement geochemical data from a wide variety of geologic materials. Rocks or other solid samples are taken into solution with a four acid digestion procedure and introduced directly into the plasma; fluid samples are acidified or analyzed directly. The entire process is computer-controlled, fully-automated, and requires less than five minutes per sample for quantitative determination of 37 elements. The procedures and instrumentation employed at the ESL for multielement ICP analysis of geologic materials are described and these are intended as a guide for evaluating analytic results reported from this laboratory. The quality of geochemical data can be characterized by precision, limits of quantitative determination, and accuracy. Precision values are a measure of the repeatability of analyses. In general, major element and analyses have precision of better than 5% and trace elements of better than 10% of the amount present. (MHR)

  17. Phonon dispersion on Ag (100) surface: A modified analytic embedded atom method study

    NASA Astrophysics Data System (ADS)

    Xiao-Jun, Zhang; Chang-Le, Chen

    2016-01-01

    Within the harmonic approximation, the analytic expression of the dynamical matrix is derived based on the modified analytic embedded atom method (MAEAM) and the dynamics theory of surface lattice. The surface phonon dispersions along three major symmetry directions , and X¯M¯ are calculated for the clean Ag (100) surface by using our derived formulas. We then discuss the polarization and localization of surface modes at points X¯ and M¯ by plotting the squared polarization vectors as a function of the layer index. The phonon frequencies of the surface modes calculated by MAEAM are compared with the available experimental and other theoretical data. It is found that the present results are generally in agreement with the referenced experimental or theoretical results, with a maximum deviation of 10.4%. The agreement shows that the modified analytic embedded atom method is a reasonable many-body potential model to quickly describe the surface lattice vibration. It also lays a significant foundation for studying the surface lattice vibration in other metals. Project supported by the National Natural Science Foundation of China (Grant Nos. 61471301 and 61078057), the Scientific Research Program Funded by Shaanxi Provincial Education Department, China (Grant No. 14JK1301), and the Specialized Research Fund for the Doctoral Program of Higher Education, China (Grant No. 20126102110045).

  18. Inelastic collisional deactivation in plasma-related non-spectroscopic matrix interferences in inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Al-Ammar, Assad S.; Barnes, Ramon M.

    1999-07-01

    Inelastic collisional deactivation of the analyte excited state is demonstrated as a dominant cause for non-spectroscopic matrix interference in inductively coupled plasma atomic emission spectrometry (ICP-AES) for commonly used plasma operating conditions in routine analysis. A mathematical simulation of the inelastic collisional model was examined. Comparison between the theoretical model and experimental results using atomic and ionic lines of the analytes Zn, Ba, Mg, Mn and Sr validates the inelastic collisional deactivation model as a dominant cause for non-spectroscopic matrix effect. Matrices evaluated were NH 4Cl, NH 4SCN, (NH 4) 2SO 4, and H 2SO 4 to represent difficult-to-ionize matrices (DIE) and NaCl and CaCl 2 to represent easy-to-ionize element matrices (EIE).

  19. Isotope ratio determination of uranium by optical emission spectroscopy on a laser-produced plasma - basic investigations and analytical results

    NASA Astrophysics Data System (ADS)

    Pietsch, W.; Petit, A.; Briand, A.

    1998-05-01

    We report in this paper, the first determination of the isotope ratio (238/235) in an uranium sample by optical emission spectroscopy on a laser-produced plasma at reduced pressure (2.67 Pa). Investigations aimed at developing a new application of laser ablation for analytical isotope control of uranium are presented. Optimized experimental conditions allow one to obtain atomic emission spectra characterized by the narrowest possible line widths of the order of 0.01 nm for the investigated transition UII 424.437 nm. We show the possibility to achieve a relative precision in the range of 5% for an enrichment of 3.5% 235U. The influence of different relevant plasma parameters on the measured line width is discussed.

  20. Atomic emission and atomic fluorescence spectroscopy in the direct current plasma

    SciTech Connect

    Hendrick, M.S.

    1985-01-01

    The Direct Current Plasma (DCP) was investigated as a source for Atomic Emission (AE) and Atomic Fluorescence Spectrometry (AFS). The DCP was optimized for AE analyses using simplex optimization and Box-Behnken partial factorial experimental design, varying argon flows, and plasma position. Results were compared with a univariate search carried out in the region of the simplex optimum. Canonical analysis demonstrated that no true optimum exists for sensitivity, precision, or drift. A stationary ridge, where combinations of conditions gave comparable instrumental responses, was found. The DCP as an excitation source for AFS in a flame was used for diagnostic studies of the DCP. Moving the aerosol introduction tube behind the DCP with respect to the flame improved the characteristics of the DCP as a narrow line source, although self-absorption was observed at high concentrations of metal salt solutions in the DCP. Detection limits for Cd, Co, Cr, Cu, Fe, Mg, Mn, Zn, and Ni were in the low ng/mL region. Theoretical expressions for scatter correction with a two-line technique were derived, although no correction was necessary to achieve accurate results for standard reference materials.

  1. Point-defect properties in HCP rare earth metals with analytic modified embedded atom potentials

    NASA Astrophysics Data System (ADS)

    Hu, Wangyu; Deng, Huiqiu; Yuan, Xiaojian; Fukumoto, Masahiro

    2003-08-01

    The analytic embedded atom method (EAM) type many-body potentials of hcp rare earth metals (Dy, Er, Gd, Ho, Nd, Pr, and Tb) have been constructed. The hcp lattice is shown to be energetically most stable when compared with the fcc and bcc structure, and the hcp lattice with ideal c/a. The mechanical stability of the corresponding hcp lattice with respect to large change of density and c/a ratio is examined. The phonon spectra, stacking fault and surface energy are calculated. The activation energy for vacancy diffusion in these metals has been calculated and the most possible diffusion paths are predicted. Finally, the self-interstitial atom (SIA) formation energy and volume have been evaluated for eight possible sites. This calculation suggests that the crowdion and basal split are the most stable configurations. The SIA formation energy increases linearly with the increase of the melting temperature.

  2. Kinetics and continuum emission of negative atomic ions in partially ionized plasmas

    NASA Technical Reports Server (NTRS)

    Soon, W. H.; Kunc, J. A.

    1991-01-01

    Kinetics and continuum emission of negative ions are studied in stationary atomic hydrogen, nitrogen, and oxygen plasmas. The intensity of the negative-ion emission was found to be neglibible when compared to those of bound-bound and free-bound emission at low and medium particle densities. However, the negative-ion continuum emission can contribute significantly in certain parts of the emission spectrum at high particle densities.

  3. Single-photon modulation by the collective emission of an atomic chain

    NASA Astrophysics Data System (ADS)

    Liao, Zeyang; Zubairy, M. Suhail

    2014-11-01

    We study the collective spontaneous emission of a linear atomic chain excited by a single photon. The interaction between the atoms and the common vacuum field can significantly change the eigenenergy and the spontaneous emission rate of the system. Due to the dipole-dipole interactions, the system prepared in a single-photon timed Dicke state is the superposition of superradiant and subradiant eigenstates that can have a nonexponential decay dynamics. We can tune the frequency and linewidth of the superradiant and subradiant emission from a timed Dicke state by changing the direction of the atomic dipole moment or the atomic separation. In addition, the emission direction of the superradiant and subradiant photons also depends on the polarization of the atoms.

  4. Analytical screening of low emissions, high performance duct burners for supersonic cruise aircraft engines

    NASA Technical Reports Server (NTRS)

    Lohmann, R. A.; Riecke, G. T.

    1977-01-01

    An analytical screening study was conducted to identify duct burner concepts capable of providing low emissions and high performance in advanced supersonic engines. Duct burner configurations ranging from current augmenter technology to advanced concepts such as premix-prevaporized burners were defined. Aerothermal and mechanical design studies provided the basis for screening these configurations using the criteria of emissions, performance, engine compatibility, cost, weight and relative risk. Technology levels derived from recently defined experimental low emissions main burners are required to achieve both low emissions and high performance goals. A configuration based on the Vorbix (Vortex burning and mixing) combustor concept was analytically determined to meet the performance goals and is consistent with the fan duct envelope of a variable cycle engine. The duct burner configuration has a moderate risk level compatible with the schedule of anticipated experimental programs.

  5. Microwave plasma atomic emission spectrometric determination of Ca, K and Mg in various cheese varieties.

    PubMed

    Ozbek, Nil; Akman, Suleyman

    2016-02-01

    Microwave plasma-atomic emission spectrometry (MP-AES) was used to determine calcium, magnesium and potassium in various Turkish cheese samples. Cheese samples were dried at 100 °C for 2 days and then digested in a mixture of nitric acid/hydrogen peroxide (3:1). Good linearities (R(2) > 0.999) were obtained up to 10 μg mL(-1) of Ca, Mg and K at 445.478 nm, 285.213 nm and 766.491 nm, respectively. The analytes in a certified reference milk powder sample were determined within the uncertainty limits. Moreover, the analytes added to the cheese samples were recovered quantitatively (>90%). All determinations were performed using aqueous standards for calibration. The LOD values for Ca, Mg and K were 0.036 μg mL(-1), 0.012 μg mL(-1) and 0.190 μg mL(-1), respectively. Concentrations of Ca, K and Mg in various types of cheese samples produced in different regions of Turkey were found between 1.03-3.70, 0.242-0.784 and 0.081-0.303 g kg(-1), respectively.

  6. Microwave plasma atomic emission spectrometric determination of Ca, K and Mg in various cheese varieties.

    PubMed

    Ozbek, Nil; Akman, Suleyman

    2016-02-01

    Microwave plasma-atomic emission spectrometry (MP-AES) was used to determine calcium, magnesium and potassium in various Turkish cheese samples. Cheese samples were dried at 100 °C for 2 days and then digested in a mixture of nitric acid/hydrogen peroxide (3:1). Good linearities (R(2) > 0.999) were obtained up to 10 μg mL(-1) of Ca, Mg and K at 445.478 nm, 285.213 nm and 766.491 nm, respectively. The analytes in a certified reference milk powder sample were determined within the uncertainty limits. Moreover, the analytes added to the cheese samples were recovered quantitatively (>90%). All determinations were performed using aqueous standards for calibration. The LOD values for Ca, Mg and K were 0.036 μg mL(-1), 0.012 μg mL(-1) and 0.190 μg mL(-1), respectively. Concentrations of Ca, K and Mg in various types of cheese samples produced in different regions of Turkey were found between 1.03-3.70, 0.242-0.784 and 0.081-0.303 g kg(-1), respectively. PMID:26304350

  7. Critical evaluation of the application of photochemical vapor generation in analytical atomic spectrometry.

    PubMed

    He, Yihua; Hou, Xiandeng; Zheng, Chengbin; Sturgeon, Ralph E

    2007-06-01

    Chemical vapor generation (CVG) is a widely adopted sample introduction method for analytical atomic spectrometry. Nonvolatile precursors (usually ionic, metallic or organometallic species) can be transferred from the condensed phase to the gas phase, yielding the advantages of efficient matrix separation, high analyte transport efficiency, high selectivity, simple instrumentation, and ease of automation. Hydride generation enjoys the greatest popularity as a consequence of its ease of implementation, fast reaction and high yield; but photo-CVG, a newly emerging research field in analytical chemistry, may provide a powerful alternative to conventional CVG due to its simplicity, versatility and cost effectiveness. Although photocatalytic pre-reduction has been used for a number of years, the most attractive aspect of this newly emerging area is the direct generation of volatile species using photochemical reactions. Recent studies undertaken with flow through and batch reactors employing low molecular weight organic acids as photochemical agents are highlighted in this study for such systems as mercury and selenium, as well as reaction mechanisms considered for these processes. Discussion is focused on recent advances in photo-CVG, which we believe will become the subject of intensive future research initiatives. PMID:17235500

  8. Spatial and temporal variations in infrared emissions of the upper atmosphere. 1. Atomic oxygen (λ 63 μm) emission

    NASA Astrophysics Data System (ADS)

    Semenov, A. I.; Medvedeva, I. V.; Perminov, V. I.; Khomich, V. Yu.

    2016-09-01

    Rocket and balloon measurement data on atomic-oxygen (λ 63 µm) emission in the upper atmosphere are presented. The data from the longest (1989-2003) period of measurements of the atomic-oxygen (λ 63 µm) emission intensity obtained by spectral instruments on sounding balloons at an altitude of 38 km at midlatitudes have been systematized and analyzed. Regularities in diurnal and seasonal variations in the intensity of this emission, as well as in its relation with solar activity, have been revealed.

  9. Two-channel emission model for collective quantum jumps in Rydberg atoms

    NASA Astrophysics Data System (ADS)

    Cayayan, Lyndon; Clemens, James

    2016-05-01

    We consider a system of driven, damped Rydberg atoms with dipole-dipole energy shifts which can give rise to a Rydberg blockade when the atoms are driven on resonance and collective quantum jumps when the atoms are driven off resonance. For the damping we consider a two-channel emission model with competition between fully independent and fully collective spontaneous emission. For independent emission a quasiclassical model predicts a bistable steady state and quantum fluctuations drive collective jumps between the two bistable branches. We show that the collective emission is enhanced, relative to the independent emission, which shifts the total effective spontaneous emission rate and impacts the presence or absence of bistability predicted by the quasiclassical model.

  10. Derivation of an analytical approximation of the spectrum of spinning dust emission

    SciTech Connect

    Stevenson, Matthew A.

    2014-02-01

    An analytical function for the spectrum of spinning dust emission is presented. It is derived through the application of careful approximations, with each step tested against numerical calculations. This approach ensures accuracy while providing an intuitive picture of the physics. The final result may be useful for fitting of anomalous microwave emission observations, as is demonstrated by a comparison with the Planck observations of the Perseus Molecular Cloud. It is hoped that this will lead to a broader consideration of the spinning dust model when interpreting microwave continuum observations, and that it will provide a standard framework for interpreting and comparing the variety of anomalous microwave emission observations.

  11. 40 CFR 86.1207-96 - Sampling and analytical systems; evaporative emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) Evaporative Emission Test Procedures for New Gasoline-Fueled, Natural Gas-Fueled, Liquefied Petroleum Gas-Fueled and Methanol-Fueled Heavy-Duty Vehicles § 86.1207-96 Sampling and analytical systems..., the enclosure shall be gas tight in accordance with § 86.1217-96. Interior surfaces must...

  12. 40 CFR 86.1207-96 - Sampling and analytical systems; evaporative emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) Evaporative Emission Test Procedures for New Gasoline-Fueled, Natural Gas-Fueled, Liquefied Petroleum Gas-Fueled and Methanol-Fueled Heavy-Duty Vehicles § 86.1207-96 Sampling and analytical systems..., the enclosure shall be gas tight in accordance with § 86.1217-96. Interior surfaces must...

  13. An analytic technique for statistically modeling random atomic clock errors in estimation

    NASA Technical Reports Server (NTRS)

    Fell, P. J.

    1981-01-01

    Minimum variance estimation requires that the statistics of random observation errors be modeled properly. If measurements are derived through the use of atomic frequency standards, then one source of error affecting the observable is random fluctuation in frequency. This is the case, for example, with range and integrated Doppler measurements from satellites of the Global Positioning and baseline determination for geodynamic applications. An analytic method is presented which approximates the statistics of this random process. The procedure starts with a model of the Allan variance for a particular oscillator and develops the statistics of range and integrated Doppler measurements. A series of five first order Markov processes is used to approximate the power spectral density obtained from the Allan variance.

  14. Experimental estimation of oxidation-induced Si atoms emission on Si(001) surfaces

    SciTech Connect

    Ogawa, Shuichi Tang, Jiayi; Takakuwa, Yuji

    2015-08-15

    Kinetics of Si atoms emission during the oxidation of Si(001) surfaces have been investigated using reflection high energy electron diffraction combined with Auger electron spectroscopy. The area ratio of the 1 × 2 and the 2 × 1 domains on a clean Si(001) surface changed with the oxidation of the surface by Langmuir-type adsorption. This change in the domain ratio is attributed to the emission of Si atoms. We can describe the changes in the domain ratio using the Si emission kinetics model, which states that (1) the emission rate is proportional to the oxide coverage, and (2) the emitted Si atoms migrate on the surface and are trapped at S{sub B} steps. Based on our model, we find experimentally that up to 0.4 ML of Si atoms are emitted during the oxidation of a Si(001) surface at 576 °C.

  15. Temperature measurement of wood flame based on the double line method of atomic emission spectra

    NASA Astrophysics Data System (ADS)

    Hao, Xiaojian; Liu, Zhenhua; Sang, Tao

    2016-01-01

    Aimed at the testing requirement of the transient high temperature in explosion field and the bore of barrel weapon, the temperature measurement system of double line of atomic emission spectrum was designed, the method of flame spectrum testing system were used for experimental analysis. The experimental study of wood burning spectra was done with flame spectrum testing system. The measured spectra contained atomic emission spectra of the elements K, Na, and the excitation ease of two kinds atomic emission spectra was analyzed. The temperature was calculated with two spectral lines of K I 766.5nm and 769.9nm. The results show that, compared with Na, the excitation temperature of K atomic emission spectra is lower. By double line method, the temperature of wood burning is 1040K, and error is 3.7%.

  16. High-pressure combustor exhaust emissions with improved air-atomizing and conventional pressure-atomizing fuel nozzles

    NASA Technical Reports Server (NTRS)

    Ingebo, R. D.; Norgren, C. T.

    1973-01-01

    A high-pressure combustor segment 0.456 meter (18 in.) long with a maximum cross section of 0.153 by 0.305 meter (6 by 12 in.) was tested with specially designed air-atomizing and conventional pressure-atomizing fuel nozzles at inlet-air temperatures of 340 to 755 k (610 deg to 1360 R), reference velocities of 12.4 to 26.1 meters per second (41 to 86 ft/sec), and fuel-air ratios of 0.008 to 0.020. Increasing inlet-air pressure from 4 to 20 atmospheres generally increased smoke number and nitric oxide, but decreased carbon monoxide and unburned hydrocarbon concentrations with air-atomizing and pressure-atomizing nozzles. Emission indexes for carbon monoxide and unburned hydrocarbons were lower at 4, 10, and 20 atmospheres, and nitric oxide emission indexes were lower at 10 and 20 atmospheres with air-atomizing than with pressure-atomizing nozzles.

  17. An analytic model for accurate spring constant calibration of rectangular atomic force microscope cantilevers.

    PubMed

    Li, Rui; Ye, Hongfei; Zhang, Weisheng; Ma, Guojun; Su, Yewang

    2015-10-29

    Spring constant calibration of the atomic force microscope (AFM) cantilever is of fundamental importance for quantifying the force between the AFM cantilever tip and the sample. The calibration within the framework of thin plate theory undoubtedly has a higher accuracy and broader scope than that within the well-established beam theory. However, thin plate theory-based accurate analytic determination of the constant has been perceived as an extremely difficult issue. In this paper, we implement the thin plate theory-based analytic modeling for the static behavior of rectangular AFM cantilevers, which reveals that the three-dimensional effect and Poisson effect play important roles in accurate determination of the spring constants. A quantitative scaling law is found that the normalized spring constant depends only on the Poisson's ratio, normalized dimension and normalized load coordinate. Both the literature and our refined finite element model validate the present results. The developed model is expected to serve as the benchmark for accurate calibration of rectangular AFM cantilevers.

  18. Analytic basis set for high-Z atomic QED calculations: Heavy He-like ions

    SciTech Connect

    Hylton, D.J.; Snyderman, N.J.

    1997-04-01

    A relativistic Sturmian analytic basis set representation for the Coulomb-Dirac Green function, previously studied by Zapryagaev, Manakov, and Pal{close_quote}chikov [Opt. Spectrosc. {bold 52}, 248 (1982)], is investigated for application to high-Z atomic QED calculations. This pseudoeigenfunction representation follows from exact identities starting from the Whittaker function representation. It eliminates the radial ordering problem of that representation, and so is particularly useful for numerical calculation of the perturbation theory Feynman diagrams with more than one electron Green function. While the Green function represents discrete bound states, and both positive and negative energy continuum states, the Sturmian (bound-state-like) form for the pseudoeigenfunctions makes it possible to more analytically calculate matrix elements for full photon exchange, reducing numerical problems for high photon frequency. For He-like Fm (Z=100) we calculate the perturbation theory equivalent of the Dirac-Fock-Breit ground-state energy, agreeing well with the Grant code and with the numerical B-spline basis set approach results of Blundell, Mohr, Johnson, and Sapirstein [Phys. Rev. A {bold 48}, 2615 (1993)]. Preliminary results on the relativistic and QED correlation are also reported. {copyright} {ital 1997} {ital The American Physical Society}

  19. An analytic model for accurate spring constant calibration of rectangular atomic force microscope cantilevers

    PubMed Central

    Li, Rui; Ye, Hongfei; Zhang, Weisheng; Ma, Guojun; Su, Yewang

    2015-01-01

    Spring constant calibration of the atomic force microscope (AFM) cantilever is of fundamental importance for quantifying the force between the AFM cantilever tip and the sample. The calibration within the framework of thin plate theory undoubtedly has a higher accuracy and broader scope than that within the well-established beam theory. However, thin plate theory-based accurate analytic determination of the constant has been perceived as an extremely difficult issue. In this paper, we implement the thin plate theory-based analytic modeling for the static behavior of rectangular AFM cantilevers, which reveals that the three-dimensional effect and Poisson effect play important roles in accurate determination of the spring constants. A quantitative scaling law is found that the normalized spring constant depends only on the Poisson’s ratio, normalized dimension and normalized load coordinate. Both the literature and our refined finite element model validate the present results. The developed model is expected to serve as the benchmark for accurate calibration of rectangular AFM cantilevers. PMID:26510769

  20. Impact of the analytical blank in the uncertainty evaluation of the copper content in waters by flame atomic absorption spectrometry.

    PubMed

    de Oliveira, Elcio Cruz; Monteiro, Maria Inês Couto; Pontes, Fernanda Veronesi Marinho; de Almeida, Marcelo Dominguez; Carneiro, Manuel Castro; da Silva, Lílian Irene Dias; Alcover Neto, Arnaldo

    2012-01-01

    Chemical analysts use analytical blanks in their analyses, but seldom is this source of uncertainty evaluated. Generally, there is great confusion. Although the numerical value of the blank, in some situations, can be negligible, its source of uncertainty cannot be. This article discusses the uncertainty contribution of the analytical blank using a numerical example of the copper content in waters by flame atomic absorption spectrometry. The results indicate that the uncertainties of the analytical blank can contribute up to 50% when the blank sample is considered in this analysis, confirming its high impact. This effect can be primarily observed where the analyte concentration approaches the lower range of the analytical curve. Even so, the blank is not always computed. Therefore, the relevance of the analytical blank can be confirmed by uncertainty evaluation.

  1. Evaluation of the temporal profiles and the analytical features of a laser ablation - Pulsed glow discharge coupling for optical emission spectrometry

    NASA Astrophysics Data System (ADS)

    González de Vega, Claudia; Bordel, Nerea; Pereiro, Rosario; Sanz-Medel, Alfredo

    2016-07-01

    The coupling of a glow discharge (GD) in pulsed mode (PGD) as secondary source for excitation/ionization of the material provided by laser ablation (LA) has been investigated using optical emission spectrometry (OES). The variation of the laser pulse delay with respect to the GD pulse allows to producing the ablation process during prepeak, plateau or afterglow GD regions. Emission properties of the LA-PGD plasma in each temporal region of the GD pulse have been evaluated for analytical lines of different elements. Resonant atomic lines have shown higher emission intensity in the prepeak region compared to non-resonant lines. Non-resonant lines showed higher enhancement of the emission intensity in the afterglow region. Moreover, the coupled LA-PGD system offered better linear correlation coefficients using a set of glass standards for calibration as well as lower detection limits (by at least a factor of two) when compared to laser induced breakdown spectroscopy.

  2. X-ray emission from charge exchange of highly-charged ions in atoms and molecules

    NASA Technical Reports Server (NTRS)

    Greenwood, J. B.; Williams, I. D.; Smith, S. J.; Chutjian, A.

    2000-01-01

    Charge exchange followed by radiative stabilization are the main processes responsible for the recent observations of X-ray emission from comets in their approach to the Sun. A new apparatus was constructed to measure, in collisions of HCIs with atoms and molecules, (a) absolute cross sections for single and multiple charge exchange, and (b) normalized X-ray emission cross sections.

  3. Methyl oleate as matrix simulacrum for the simultaneous determination of metals in biodiesel samples by flame atomic emission spectroscopy.

    PubMed

    Ferreira, Conny Cerai; Costa, Letícia Malta; Barbeira, Paulo Jorge Sanches

    2015-06-01

    A measurement procedure for direct and simultaneous quantification of Na, K and Ca in biodiesel by flame atomic emission spectroscopy (FAES) was developed. A lab-made device was constructed by coupling a nebulizer/combustion system from a commercial photometer to a continuous emission detector in a spectral range of 255 to 862 nm. Instrumental optimizations were carried out evaluating the most important variables, such as gas flow rates and sample introduction temperature, indicating that a temperature of 50°C enhances the analytical signals and assures good precision. The direct analysis method was properly validated and presented limits of quantification of 0.09, 0.07 and 0.43 μg kg(-1) for Na, K and Ca, respectively. Accuracy of the proposed procedure was checked by comparing the results with those obtained by the standard procedure described in ABNT NBR 15556 and the standard addition method. PMID:25863364

  4. Kennard-Stepanov relation connecting absorption and emission spectra in an atomic gas.

    PubMed

    Moroshkin, Peter; Weller, Lars; Sass, Anne; Klaers, Jan; Weitz, Martin

    2014-08-01

    The Kennard-Stepanov relation describes a thermodynamic, Boltzmann-type scaling between the absorption and emission spectral profiles of an absorber, which applies in many liquid state dye solutions as well as in semiconductor systems. Here we examine absorption and emission spectra of rubidium atoms in a dense argon buffer gas environment. We demonstrate that the Kennard-Stepanov relation between absorption and emission spectra is well fulfilled in the collisionally broadened atomic gas system. Our experimental findings are supported by a simple theoretical model.

  5. Coherent control of cooperative spontaneous emission from two identical three-level atoms in a photonic crystal

    NASA Astrophysics Data System (ADS)

    Woldeyohannes, Mesfin; Idehenre, Ighodalo; Hardin, Tyler

    2015-08-01

    The coherent control of cooperative spontaneous emission from two identical non-overlapping three-level atoms in the V-configuration located within a photonic band gap (PBG) material with two resonant frequencies near the upper band edge of the PBG and confined to a region small in comparison to their radiation wavelengths but still greater than their atomic sizes is investigated. The dependencies of cooperative effects in which a photon emitted by one atom is reabsorbed by the other atom on the inter-atomic separation, on the initial state of the two-atom system, on the strength of the driving control laser field, and on the detuning of the atomic resonant frequencies from the upper band edge frequency is analyzed so as to identify the conditions for which these cooperative effects are enhanced or inhibited. Cooperative effects between atoms are shown to be influenced more by the PBG than by the nature of the atomic transitions involved. Excited state populations as well as coherences between excited levels are expressed in terms of time-dependent amplitudes which are shown to satisfy coupled integro-differential equations for which analytic solutions are derived under special conditions. Unlike for the case of one atom in a PBG where the fractional non-zero steady state populations on the excited levels as well as the coherence between the excited levels are constants independent of time, in the case of two atoms in PBG these quantities continuously oscillate as a manifestation of beating due to the continuous exchange between the two atoms of the photon trapped by the PBG. The values of these quantities as well as the amplitudes and frequencies of their oscillations depend of the parameters of the system, providing different ways of manipulating the system. The general formalism presented here is shown to recapture the special results of investigations of similar systems in free space when the non-Markovian memory kernels of the PBG are replaced by delta

  6. Analytic expressions for atomic layer deposition: Coverage, throughput, and materials utilization in cross-flow, particle coating, and spatial atomic layer deposition

    SciTech Connect

    Yanguas-Gil, Angel; Elam, Jeffrey W.

    2014-05-15

    In this work, the authors present analytic models for atomic layer deposition (ALD) in three common experimental configurations: cross-flow, particle coating, and spatial ALD. These models, based on the plug-flow and well-mixed approximations, allow us to determine the minimum dose times and materials utilization for all three configurations. A comparison between the three models shows that throughput and precursor utilization can each be expressed by universal equations, in which the particularity of the experimental system is contained in a single parameter related to the residence time of the precursor in the reactor. For the case of cross-flow reactors, the authors show how simple analytic expressions for the reactor saturation profiles agree well with experimental results. Consequently, the analytic model can be used to extract information about the ALD surface chemistry (e.g., the reaction probability) by comparing the analytic and experimental saturation profiles, providing a useful tool for characterizing new and existing ALD processes.

  7. [Determination of trace zirconium and hafniumin sample by atomic emission spectrometry].

    PubMed

    Li, Hui-zhi; Yang, Chun-xia; Zhai, Dian-tang

    2005-02-01

    This paper describes the determination of trace Zr and Hf in the sample using carbon powder and titanium oxide as the buffer by Atomic Emission Spectrometry (AES). Titanium was selected for the internal standard line. Sample separation and chemical treatment were not required. The sample was directly loaded into an ordinary electrode. The method is simple, rapid and accurate. The conditions for the determination, and the factors of influence have been studied. A new method has been developed for the determination of zirconium and hafnium. The analytical lines of Zr and Hf were 327.3 and 286.6 nm respectively. The internal standard line of Ti was 308.8 nm. The linear range of the determination of Zr and Hf was 0-0.50% and 0-0.25% respectively. The detection limit of Zr and Hf was 0.0010% and 0.010% respectively. The range of the recovery of zirconium and hafnium was 96.67%-105.0%. The results for these elements in standard sample are in agreement with certified values with a precision of 3.61% RSD for Zr (n = 9), and 4.82% RSD for Hf (n = 9). The method has been applied to the determination of Zr and Hf with satisfactory results.

  8. Laser Ablation Solid Sampling processes investigated usinginductively coupled plasma - atomic emission spectroscopy (ICP-AES)

    SciTech Connect

    Mao, X.L.; Ciocan, A.C.; Borisov, O.V.; Russo, R.E.

    1997-07-01

    The symbiotic relationship between laser ablation mechanismsand analytical performance using inductively coupled plasma-atomicemission spectroscopy are addressed in this work. For both cases, it isimportant to ensure that the ICP conditions (temperature and electronnumber density) are not effected by the ablated mass. By ensuring thatthe ICP conditions are constant, changes in spectral emission intensitywill be directly related to changes in laser ablation behavior. Mg ionicline to atomic line ratios and excitation temperature were measured tomonitor the ICP conditions during laser-ablation sample introduction. Thequantity of ablated mass depends on the laser pulse duration andwavelength. The quantity of mass removed per unit energy is larger whenablating with shorter laser wavelengths and pulses. Preferential ablationof constituents from a multicomponent sample was found to depend on thelaser beam properties (wavelength and pulse duration). Fornanosecond-pulsed lasers, thermal vaporization dominates the ablationprocess. For picosecond-pulsed lasers, a non-thermal mechanism appears todominate the ablation process. This work will describe the mass ablationbehavior during nanosecond and picosecond laser sampling into the ICP.The behavior of the ICP under mass loading conditions is firstestablished, followed by studies of the ablation behavior at variouspower densities. A thermal vaporization model is used to explainnanosecond ablation, and a possible non-thermal mechanism is proposed toexplain preferential ablation of Zn and Cu from brass samples duringpicosecond ablation.

  9. Quantification of the Rubidium in Beverage Products Micro Samples by Platinum-wire Loop in Flame Atomization Atomic Emission Spectrometry.

    PubMed

    Kékedy-Nagy, Ladislau; Zsigmond, Andreea R; Cordoş, Emil A

    2010-12-01

    The rubidium content in 3 µL of some beverage products (beer, wine, vegetable and fruit juices) atomized from a Ptwire in the methaneair flame has been determined by atomic emission spectrometry. The flame atomization conditions of rubidium were optimized, they are: λ = 780.0 nm, the height of 8 mm over the burner head, gas flow rates of 300 L h-1 air and 34 L h-1 methane. The effect of Na, K, Cs, Sr and acetone on the emission of rubidium was studied too. The limit of quantification (6σ) obtained is of 4.3±1.8 pg in the presence of 50 mg L-1 K and 5% v/v acetone (P = 0.05). The rubidium content of the samples has been determined with continuous nebulization and by atomization from the Ptwire, using the standard calibration curve and the standard addition method. The results of the two procedures agree within the determination errors. PMID:24061895

  10. Characteristics of Spontaneous Emission of Polarized Atoms in Metal Dielectric Multiple Layer Structures

    NASA Astrophysics Data System (ADS)

    Zhao, Li-Ming; Gu, Ben-Yuan; Zhou, Yun-Song

    2007-11-01

    The spontaneous emission (SE) progress of polarized atoms in a stratified structure of air-dielectric(D0)-metal(M)-dielectric(D1)-air can be controlled effectively by changing the thickness of the D1 layer and rotating the polarized direction of atoms. It is found that the normalized SE rate of atoms located inside the D0 layer crucially depends on the atomic position and the thickness of the D1 layer. When the atom is located near the D0-M interface, the normalized atomic SE rate as a function of the atomic position is abruptly onset for the thin D1 layer. However, with the increasing thickness of the D1 layer, the corresponding curve profile exhibits plateau and stays nearly unchanged. The substantial change of the SE rate stems from the excitation of the surface plasmon polaritons in metal-dielectric interface, and the feature crucially depends on the thickness of D1 layer. If atoms are positioned near the D0-air interface, the substantial variation of the normalized SE rate appears when rotating the polarized direction of atoms. These findings manifest that the atomic SE processes can be flexibly controlled by altering the thickness of the dielectric layer D1 or rotating the orientation of the polarization of atoms.

  11. Dielectric barrier discharge carbon atomic emission spectrometer: universal GC detector for volatile carbon-containing compounds.

    PubMed

    Han, Bingjun; Jiang, Xiaoming; Hou, Xiandeng; Zheng, Chengbin

    2014-01-01

    It was found that carbon atomic emission can be excited in low temperature dielectric barrier discharge (DBD), and an atmospheric pressure, low power consumption, and compact microplasma carbon atomic emission spectrometer (AES) was constructed and used as a universal and sensitive gas chromatographic (GC) detector for detection of volatile carbon-containing compounds. A concentric DBD device was housed in a heating box to increase the plasma operation temperature to 300 °C to intensify carbon atomic emission at 193.0 nm. Carbon-containing compounds directly injected or eluted from GC can be decomposed, atomized, and excited in this heated DBD for carbon atomic emission. The performance of this new optical detector was first evaluated by determination of a series of volatile carbon-containing compounds including formaldehyde, ethyl acetate, methanol, ethanol, 1-propanol, 1-butanol, and 1-pentanol, and absolute limits of detection (LODs) were found at a range of 0.12-0.28 ng under the optimized conditions. Preliminary experimental results showed that it provided slightly higher LODs than those obtained by GC with a flame ionization detector (FID). Furthermore, it is a new universal GC detector for volatile carbon-containing compounds that even includes those compounds which are difficult to detect by FID, such as HCHO, CO, and CO2. Meanwhile, hydrogen gas used in conventional techniques was eliminated; and molecular optical emission detection can also be performed with this GC detector for multichannel analysis to improve resolution of overlapped chromatographic peaks of complex mixtures. PMID:24328147

  12. Hydrogen transport diagnostics by atomic and molecular emission line profiles simultaneously measured for large helical device

    SciTech Connect

    Fujii, K.; Shikama, T.; Hasuo, M.; Goto, M.; Morita, S.

    2013-01-15

    We observe the Balmer-{alpha}, -{beta}, and -{gamma} lines of hydrogen atoms and Q branches of the Fulcher-{alpha} band of hydrogen molecules simultaneously with their polarization resolved for large helical device. From the fit including the line splits and the polarization dependences by the Zeeman effect, the emission locations, intensities, and the temperatures of the atoms and molecules are determined. The emission locations of the hydrogen atoms are determined outside but close to the last closed flux surface (LCFS). The results are consistent with a previous work (Phys. Plasmas 12, 042501 (2005)). On the other hand, the emission locations of the molecules are determined to be in the divertor legs, which is farer from those of the atoms. The kinetic energy of the atoms is 1 {approx} 20 eV, while the rotational temperature of molecules is {approx}0.04 eV. Additionally, substantial wings, which originate from high velocity atoms and are not reproduced by the conventional spectral analysis, are observed in the Balmer line profiles. We develop a one-dimensional model to simulate the transport of the atoms and molecules. The model reproduces the differences of the emission locations of the atoms and molecules when their initial temperatures are assumed to be 3 eV and 0.04 eV, respectively. From the model, the wings of the Balmer-{alpha} line is attributed to the high velocity atoms exist deep inside the LCFS, which are generated by the charge exchange collisions with hot protons there.

  13. Elemental determination of microsamples by liquid film dielectric barrier discharge atomic emission spectrometry.

    PubMed

    He, Qian; Zhu, Zhenli; Hu, Shenghong; Zheng, Hongtao; Jin, Lanlan

    2012-05-01

    In this study, a new liquid-film dielectric barrier discharge (LFDBD) atomic emission source was developed for microsample elemental determination. It consists of a copper electrode, a tungsten wire electrode, and a piece of glass slide between them, which serves as the dielectric barrier as well as the sample plate. The sample solution with 1 mol L(-1) nitric acid, when deposited onto the surface of the glass slide, forms a thin liquid film. The plasma is generated between the tip of the tungsten wire electrode and the liquid film surface when alternating-current (ac) high voltage (peak voltage ~3.7 kV, frequency ~30 kHz) is applied on the electrodes. Qualitative and quantitative determinations of metal ions in the sample solution were achieved by atomic emission measurements in the plasma and were demonstrated in this study with elements Na, K, Cu, Zn, and Cd. Detection limits were in the range from 0.6 ng (7 μg L(-1)) for Na to 6 ng (79 μg L(-1)) for Zn. Repeatability, expressed as relative standard deviation from seven repetitive analyses of samples with analyte concentrations at 1 mg L(-1), varied from 2.1% to 4.4%. Compared with other liquid discharge systems that operate at atmospheric pressure, the current system offers several advantages: First, it eliminates the use of a sample flow system (e.g., syringe or peristaltic pump); instead, a small aliquot of sample is directly pipetted onto the glass slide for analysis. Second, it is a microanalysis system and requires sample volume ≤80 μL, a benefit when a limited amount of sample is available. Third, because the sample is applied in aliquot, there is no washout time, and the analysis can be easily extended to sample array for high-throughput analysis. The proposed LFDBD is promising for in-field elemental determination because of its simplicity, cost effectiveness, low power supply, and no inert gas requirement. PMID:22486234

  14. Characterization of hydrocarbon emissions from green sand foundry core binders by analytical pyrolysis

    SciTech Connect

    Yujue Wang; Fred S. Cannon; Magda Salama; Jeff Goudzwaard; James C. Furness

    2007-11-15

    Analytical pyrolysis was conducted to compare the hydrocarbon and greenhouse gas emissions of three foundry sand binders: (a) conventional phenolic urethane resin, (b) biodiesel phenolic urethane resin, and (c) collagen-based binder. These binders are used in the metal casting industry to create internal cavities within castings. Green sand contains silica sand, clay, carbonaceous additives (eg bituminous coal) and water. The core samples were flash pyrolyzed in a Curie-point pyrolyzer at 920{sup o}C with a heating rate of about 3000{sup o}C/sec. This simulated some key features of the fast heating conditions that the core binders would experience at the metal-core interface when molten metal is poured into green sand molds. The core samples were also pyrolyzed in a thermogravimetric analyzer (TGA) from ambient temperature to 1000{sup o}C with a heating rate of 30{sup o}C/min, and this simulated key features of the slow heating conditions that the core binders would experience at distances that are further away from the metal-core interface during casting cooling. Hydrocarbon emissions from flash pyrolysis were analyzed with a gas chromatography-flame ionization detector, while hydrocarbon and greenhouse gas emissions from TGA pyrolysis were monitored with mass spectrometry. The prominent hazardous air pollutant emissions during pyrolysis of the three binders were phenol, cresols, benzene, and toluene for the conventional phenolic urethane resin and biodiesel resin, and benzene and toluene for the collagen-based binder. Bench-scale analytical pyrolysis techniques could be a useful screening tool for the foundries to compare the relative emissions of alternative core binders and to choose proper materials in order to comply with air-emission regulations. 20 refs., 4 figs., 1 tab.

  15. LASER ABLATION-INDUCTIVELY COUPLED PLASMA-ATOMIC EMISSION SPECTROSCOPY STUDY AT THE 222-S LABORATORY USING HOT-CELL GLOVE BOX PROTOTYPE SYSTEM

    SciTech Connect

    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.

  16. [Experimental study on flame temperature measurement by double line of atomic emission spectroscopy].

    PubMed

    Chen, Xiao-Bin; Cai, Xiao-Shu; Fan, Xue-Liang; Shen, Jia-Qi

    2009-12-01

    The flame temperature was measured by the double line of atomic emission spectroscopy according to the spectra of K (766.5 and 769.9 nm) whose relative intensity was obtained by fiber spectrometer. The principles, methods and experiment system were described. The temperature measured by the double line of atomic emission spectroscopy was compared to the results measured by thermal couple under the condition of thermal equilibrium of blackbody furnace. The comparison indicated a good coherence between these two measurement methods. The method was demonstrated on coal powder and timber, and the temperature measured corresponded to reality. PMID:20210126

  17. Slurry sample introduction with microwave induced plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Matusiewicz, Henryk; Sturgeon, Ralph E.

    1993-04-01

    The successful direct introduction of aqueous slurry samples into a highly efficient TE 101 microwave plasma has been demonstrated. Slurry samples from a spray chamber are fed directly into the cavity with no desolvation apparatus. A V-groove, clog-free Babington-type nebulizer was evaluated for use with high solids content solutions. Slurry concentrations up to 10% m/v were used for the microwave induced plasma work with calibration by the standard additions method. Results are presented for the analysis of two NRCC Standard Reference Materials, i.e. TORT-1 (Lobster Hepatopancreas) and PACS-21 (Marine Sediment). Agreement between analytical results and certified values for the test elements Cd, Cu, Fe and Zn (in the range of 28-850 μg/g) was good. No memory effects were evident and the nebulizer system had a rapid clean-out time.

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

    PubMed

    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.

  19. Real-time atomic absorption mercury continuous emission monitor

    NASA Astrophysics Data System (ADS)

    Zamzow, Daniel S.; Bajic, Stanley J.; Eckels, David E.; Baldwin, David P.; Winterrowd, Chris; Keeney, Robert

    2003-08-01

    A continuous emission monitor (CEM) for mercury (Hg) in combustor flue gas streams has been designed and tested for the detection of Hg by optical absorption. A sampling system that allows continuous introduction of stack gas is incorporated into the CEM, for the sequential analysis of elemental and total Hg. A heated pyrolysis tube is used in the system to convert oxidized Hg compounds to elemental Hg for analysis of total Hg; the pyrolysis tube is bypassed to determine the elemental Hg concentration in the gas stream. A key component of the CEM is a laboratory-designed and -assembled echelle spectrometer that provides simultaneous detection of all of the emission lines from a Hg pen lamp, which is used as the light source for the optical absorption measurement. This feature allows for on-line spectroscopic correction for interferent gases such as sulfur dioxide and nitrogen dioxide, typically present in combustion stack gas streams, that also absorb at the Hg detection wavelength (253.65 nm). This article provides a detailed description of the CEM system, the characteristics and performance of the CEM, and the results of field tests performed at the Environmental Protection Agency-Rotary Kiln at Research Triangle Park, NC.

  20. Characterization of hydrocarbon emissions from green sand foundry core binders by analytical pyrolysis.

    PubMed

    Wang, Yujue; Cannon, Fred S; Salama, Magda; Goudzwaard, Jeff; Furness, James C

    2007-11-15

    Analytical pyrolysis was conducted to study a relative comparison of the hydrocarbon and greenhouse gas emissions of three foundry sand binders as follows: (a) conventional phenolic urethane resin, (b) biodiesel phenolic urethane resin, and (c) collagen-based binder. These binders are used in the metal casting industry for making cores that are used to create internal cavities within castings. In this study, the core samples were flash pyrolyzed in a Curie-point pyrolyzer at 920 degrees C with a heating rate of about 3000 degrees C/sec. This simulated some key features of the fast heating conditions that the core binders would experience at the metal-core interface when molten metal is poured into green sand molds. The core samples were also pyrolyzed in a thermogravimetric analyzer (TGA) from ambient temperature to 1000 degrees C with a heating rate of 30 degrees C/min, and this simulated key features of the slow heating conditions that the core binders would experience at distances that are further away from the metal-core interface during casting cooling. Hydrocarbon emissions from flash pyrolysis were analyzed with a gas chromatography-flame ionization detector, while hydrocarbon and greenhouse gas (CO and CO2) emissions from TGA pyrolysis were monitored with mass spectrometry. The prominent hazardous air pollutant emissions during pyrolysis of the three binders were phenol, cresols, benzene, and toluene for the conventional phenolic urethane resin and biodiesel resin, and they were benzene and toluene for the collagen-based binder. It was also found that volatile organic compound and polycyclic aromatic hydrocarbon emissions considerably decreased in order from conventional phenolic urethane resin to biodiesel resin to collagen-based binder. These results have shown some similarity with those for stack emission testing conducted at demonstration scale and/or full-scale foundries, and the similar trends in the two sets of results offered promise that bench

  1. Cadmium, copper, lead, and zinc determination in precipitation: A comparison of inductively coupled plasma atomic emission spectrometry and graphite furnace atomization atomic absorption spectrometry

    USGS Publications Warehouse

    Reddy, M.M.; Benefiel, M.A.; Claassen, H.C.

    1987-01-01

    Selected trace element analysis for cadmium, copper, lead, and zinc in precipitation samples by inductively coupled plasma atomic emission Spectrometry (ICP) and by atomic absorption spectrometry with graphite furnace atomization (AAGF) have been evaluated. This task was conducted in conjunction with a longterm study of precipitation chemistry at high altitude sites located in remote areas of the southwestern United States. Coefficients of variation and recovery values were determined for a standard reference water sample for all metals examined for both techniques. At concentration levels less than 10 micrograms per liter AAGF analyses exhibited better precision and accuracy than ICP. Both methods appear to offer the potential for cost-effective analysis of trace metal ions in precipitation. ?? 1987 Springer-Verlag.

  2. Variations in the atomic oxygen 630 nm emission intensity related to orography

    NASA Astrophysics Data System (ADS)

    Nasyrov, G. A.

    2009-08-01

    The spatial variations in the emission intensity, related to internal gravity waves (IGWs) generated in the troposphere when the air flows around the Kopet Dagh mountain range, and the regularities of these variations have been detected for the first time based on the photometric measurements of the spatial distribution of the atomic oxygen 630 nm emission intensity, performed in 1967 at Vannovskii station of the Physicotechnical Institute, Academy of Sciences of the Turkmen SSR.

  3. Atomic carbon emission from photodissociation of CO2. [planetary atmospheric chemistry

    NASA Technical Reports Server (NTRS)

    Wu, C. Y. R.; Phillips, E.; Lee, L. C.; Judge, D. L.

    1978-01-01

    Atomic carbon fluorescence, C I 1561, 1657, and 1931 A, has been observed from photodissociation of CO2, and the production cross sections have been measured. A line emission source provided the primary photons at wavelengths from threshold to 420 A. The present results suggest that the excited carbon atoms are produced by total dissociation of CO2 into three atoms. The cross sections for producing the O I 1304-A fluorescence through photodissociation of CO2 are found to be less than 0.01 Mb in the wavelength region from 420 to 835 A. The present data have implications with respect to photochemical processes in the atmospheres of Mars and Venus.

  4. Multiple scattering of matter waves: An analytic model of the refractive index for atomic and molecular gases

    SciTech Connect

    Lemeshko, Mikhail; Friedrich, Bretislav

    2010-08-15

    We present an analytic model of the refractive index for matter waves propagating through atomic or molecular gases. The model, which combines the Wentzel-Kramers-Brillouin (WKB) treatment of the long-range attraction with the Fraunhofer model treatment of the short-range repulsion, furnishes a refractive index in compelling agreement with recent experiments of Jacquey et al. [Phys. Rev. Lett. 98, 240405 (2007)] on Li atom matter waves passing through dilute noble gases. We show that the diffractive contribution, which arises from scattering by a two-dimensional 'hard core' of the potential, is essential for obtaining a correct imaginary part of the refractive index.

  5. Chemical Analysis of Impurity Boron Atoms in Diamond Using Soft X-ray Emission Spectroscopy

    SciTech Connect

    Muramatsu, Yasuji; Iihara, Junji; Takebe, Toshihiko; Denlinger, Jonathan D.

    2008-03-29

    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 molecular orbital calculations confirm that boron atoms in CVD-B-diamond substitute for carbon atoms in the diamond lattice to form covalent B-C bonds, while boron atoms in HPT-B-diamond react with the impurity nitrogen atoms to form hexagonal boron nitride. This suggests that the high purity diamond without nitrogen impurities is necessary to synthesize p-type B-diamond semiconductors.

  6. Spontaneous emission from a microwave-driven four-level atom in an anisotropic photonic crystal

    NASA Astrophysics Data System (ADS)

    Jiang, Li; Wan, Ren-Gang; Yao, Zhi-Hai

    2016-10-01

    The spontaneous emission from a microwave-driven four-level atom embedded in an anisotropic photonic crystal is studied. Due to the modified density of state (DOS) in the anisotropic photonic band gap (PBG) and the coherent control induced by the coupling fields, spontaneous emission can be significantly enhanced when the position of the spontaneous emission peak gets close to the band gap edge. As a result of the closed-loop interaction between the fields and the atom, the spontaneous emission depends on the dynamically induced Autler-Townes splitting and its position relative to the PBG. Interesting phenomena, such as spectral-line suppression, enhancement and narrowing, and fluorescence quenching, appear in the spontaneous emission spectra, which are modulated by amplitudes and phases of the coherently driven fields and the effect of PBG. This theoretical study can provide us with more efficient methods to manipulate the atomic spontaneous emission. Project supported by the National Natural Science Foundation of China (Grant Nos. 11447232, 11204367, 11447157, and 11305020).

  7. HPLC-ICP atomic emission spectrometry in environmental analysis

    SciTech Connect

    Frame, E.M.S.

    1996-10-01

    Trace concentrations of many compounds are difficult to determine directly by traditional chromatographic techniques. Organosilicon compounds, for example, have no chromophoric groups. Size exclusion (SEC) and high performance liquid chromatography (HPLC) can separate high and low molecular weight organosilicon compounds, but routinely employ detectors with insufficient sensitivity for trace concentrations in environmental samples. Elemental analysis methods such as inductively coupled plasma optical emission spectrometry (ICP) provide excellent element sensitivity but no speciation information. Interfacing of a chromatographic method with ICP has been shown to provide quantitative determination of trace compounds while retaining the chemical speciation information. This work will describe the power of the HPLC-ICP combination for trace compounds in environmental samples to identify and determine ppm levels of organometallics.

  8. Oxygen dayglow emissions as proxies for atomic oxygen and ozone in the mesosphere and lower thermosphere

    NASA Astrophysics Data System (ADS)

    Yankovsky, Valentine A.; Martyshenko, Kseniia V.; Manuilova, Rada O.; Feofilov, Artem G.

    2016-09-01

    The main goal of this study is to propose and then to justify a set of methods for retrieving the [O] and [O3] altitude distributions from the observation of emissions of the excited oxygen molecules and O(1D) atom at daytime in the mesosphere and lower thermosphere (MLT) region. In other words, we propose retrieving the [O] and [O3] using the proxies. One of the main requirements for the proxy is that the measured value should be directly related to a variable of our interest while, at the same time, the influence of the proxies on [O3] and [O(3P)] should be minimal. For a comprehensive analysis of different O3 and O(3P) proxies, we use a full model of electronic vibrational kinetics of excited products of O3 and O2 photolysis in the MLT of the Earth. Based on this model, we have tested five excited components; namely, O2(b1Σg+, v = 0, 1, 2), O2(a1Δg , v = 0) and O(1D) as the [O3] and [O(3P)] proxies in the MLT region. Using an analytical approach to sensitivity studies and uncertainty analysis, we have therefore developed the following methods of [O(3P)] and [O3] retrieval, which utilise electronic-vibrational transitions from the oxygen molecule second singlet level (O2(b1 Σg+, v = 0, 1, 2). We conclude that O2(b1 Σg+, v = 2) and O2(b1 Σg+, v = 0) are preferable proxies for [O(3P)] retrieval in the altitude range of 90-140 km, while O2(b1 Σg+, v = 1) is the best proxy for [O3] retrieval in the altitude range of 50-98 km.

  9. Cobalt as chemical modifier to improve chromium sensitivity and minimize matrix effects in tungsten coil atomic emission spectrometry.

    PubMed

    Silva, Sidnei G; Donati, George L; Santos, Luana N; Jones, Bradley T; Nóbrega, Joaquim A

    2013-05-30

    Cobalt is used as chemical modifier to improve sensitivity and minimize matrix effects in Cr determinations by tungsten coil atomic emission spectrometry (WCAES). The atomizer is a tungsten filament extracted from microscope light bulbs. A solid-state power supply and a handheld CCD-based spectrometer are also used in the instrumental setup. In the presence of 1000 mg L(-1) Co, WCAES limit of detection for Cr (λ=425.4 nm) is calculated as 0.070 mg L(-1); a 10-fold improvement compared to determinations without Co modifier. The mechanism involved in such signal enhancement is similar to the one observed in ICP OES and ICP-MS determinations of As and Se in the presence of C. Cobalt increases the population of Cr(+) by charge transfer reactions. In a second step, Cr(+)/e(-) recombination takes place, which results in a larger population of excited-state Cr atoms. This alternative excitation route is energetically more efficient than heat transfer from atomizer and gas phase to analyte atoms. A linear dynamic range of 0.25-10 mg L(-1) and repeatability of 3.8% (RSD, n=10) for a 2.0 mg L(-1) Cr solution are obtained with this strategy. The modifier high concentration also contributes to improving accuracy due to a matrix-matching effect. The method was applied to a certified reference material of Dogfish Muscle (DORM-2) and no statistically significant difference was observed between determined and certified Cr values at a 95% confidence level. Spike experiments with bottled water samples resulted in recoveries between 93% and 112%.

  10. Solid phase microextraction capillary gas chromatography combined with furnace atomization plasma emission spectrometry for speciation of mercury in fish tissues

    NASA Astrophysics Data System (ADS)

    Grinberg, Patricia; Campos, Reinaldo C.; Mester, Zoltan; Sturgeon, Ralph E.

    2003-03-01

    The use of solid phase microextraction in conjunction with tandem gas chromatography-furnace atomization plasma emission spectrometry (SPME-GC-FAPES) was evaluated for the determination of methylmercury and inorganic mercury in fish tissue. Samples were digested with methanolic potassium hydroxide, derivatized with sodium tetraethylborate and extracted by SPME. After the SPME extraction, species were separated by GC and detected by FAPES. All experimental parameters were optimized for best separation and analytical response. A repeatability precision of typically 2% can be achieved with long-term (3 months) reproducibility precision of 4.3%. Certified Reference Materials DORM-2, DOLT-2 and TORT-2 from the National Research Council of Canada were analyzed to verify the accuracy of this technique. Detection limits of 1.5 ng g -1 for methylmercury and 0.7 ng g -1 for inorganic mercury in biological tissues were obtained.

  11. In situ calibration of inductively coupled plasma-atomic emission and mass spectroscopy

    DOEpatents

    Braymen, Steven D.

    1996-06-11

    A method and apparatus for in situ addition calibration of an inductively coupled plasma atomic emission spectrometer or mass spectrometer using a precision gas metering valve to introduce a volatile calibration gas of an element of interest directly into an aerosol particle stream. The present situ calibration technique is suitable for various remote, on-site sampling systems such as laser ablation or nebulization.

  12. Atomic emission line wavelength calculations below 2000 angstroms for Lithium II through Cobalt XXVI

    NASA Technical Reports Server (NTRS)

    Williams, M. D.

    1971-01-01

    Atomic-emission-line wavelengths are presented which were calculated from wavelengths of previously identified transition sequences using second-degree polynomials fitted to known wave numbers by the least squares method. Wavelengths less than 2000 angstroms are included for ions from Li II to Co XXVI. The computer program written in FORTRAN 4 is also included.

  13. Determination of microelements in uncontaminated natural water from the Baikal region by atomic emission spectrometry

    SciTech Connect

    Kuznetsova, A.I.; Chumakova, N.L.

    1995-10-01

    In this study, concentration by evaporation was used to determine 17 microelements (B, Al, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Sr, Mo, Ag, Sn, Ba, and Pb) in water from Lake Baikal and its tributaries by atomic-emission spectrometry with the arc excitation of spectra.

  14. Atomic emission lines in the near ultraviolet; hydrogen through krypton, section 1

    NASA Technical Reports Server (NTRS)

    Kelly, R. L.

    1979-01-01

    A compilation of spectra from the first 36 elements was prepared from published literature available through October 1977. In most cases, only those lines which were actually observed in emission or absorption are listed. The wavelengths included range from 2000 Angstroms to 3200 Angstroms with some additional lines up to 3500 Angstroms. Only lines of stripped atoms are reported; no molecular bands are included.

  15. Atomic emission lines in the near ultraviolet; hydrogen through krypton, section 2

    NASA Technical Reports Server (NTRS)

    Kelly, R. L.

    1979-01-01

    A compilation of spectra from the first 36 elements was prepared from published literature available through October 1977. In most cases, only those lines which were actually observed in emission or absorption are listed. The wavelengths included range from 2000 Angstroms to 3200 Angstroms with some additional lines up to 3500 Angstroms. Only lines of stripped atoms are reported; no molecular bands are included.

  16. Emission of energetic neutral atoms from water ice under Ganymede surface-like conditions

    NASA Astrophysics Data System (ADS)

    Wieser, Martin; Futaana, Yoshifumi; Barabash, Stas; Wurz, Peter

    2016-05-01

    The co-rotating plasma around Jupiter precipitates on the surfaces of the jovian moons, where it is not hindered by a local magnetic field. Precipitating ions lead to the emission of energetic neutral atoms, which are produced via backscattering and sputtering processes, from the surface. The European Space Agency's JUICE mission to Jupiter carries as part of the Particle Environment Package experiment an imaging energetic neutral atom spectrometer called the jovian Neutrals Analyzer (JNA). When it is in orbit around Ganymede, JNA will measure the energetic neutral atom flux emitted from the surface of Ganymede in the energy range from 10 eV to 3300 eV. The surface of Ganymede consists of a large fraction of water ice. To characterize the expected energetic neutral atom fluxes from water ice due to precipitating jovian plasma, we impacted protons and singly charged oxygen ions with energies up to 33 keV on a salty water ice target kept at Ganymede surface conditions. Emitted energetic atoms were measured energy- and mass-resolved using the JNA prototype instrument. The data show high yields for energetic neutral atoms per incident ion in the JNA energy range. For incident protons, energetic neutral atom yields between 0.28 at 1 keV and ∼40 at 33 keV were observed. For incident singly charged oxygen ions, the observed energetic neutral atom yield ranged from 0.8 for at 3 keV to ∼170 at 23 keV.

  17. Direct determination of sodium, potassium, chromium and vanadium in biodiesel fuel by tungsten coil atomic emission spectrometry.

    PubMed

    Dancsak, Stacia E; Silva, Sidnei G; Nóbrega, Joaquim A; Jones, Bradley T; Donati, George L

    2014-01-01

    High levels of sodium and potassium can be present in biodiesel fuel and contribute to corrosion, reduced performance and shorter engine lifetime. On the other hand, trace amounts of chromium and vanadium can increase the emission of pollutants during biodiesel combustion. Sample viscosity, immiscibility with aqueous solutions and high carbon content can compromise biodiesel analyzes. In this work, tungsten filaments extracted from microscope light bulbs are used to successively decompose biodiesel's organic matrix, and atomize and excite the analytes to determine sodium, potassium, chromium and vanadium by tungsten coil atomic emission spectrometry (WCAES). No sample preparation other than simple dilution in methanol or ethanol is required. Direct analysis of 10-μL sample aliquots using heating cycles with less than 150 s results in limits of detection (LOD) as low as 20, 70, 70 and 90 μg kg(-1) for Na, K, Cr and V, respectively. The procedure's accuracy is checked by determining Na and K in a biodiesel reference sample and carrying out spike experiments for Cr and V. No statistically significant differences were observed between reference and determined values for all analytes at a 95% confidence level. The procedure was applied to three different biodiesel samples and concentrations between 6.08 and 95.6 mg kg(-1) for Na and K, and between 0.22 and 0.43 mg kg(-1) for V were obtained. The procedure is simple, fast and environmentally friendly. Small volumes of reagents, samples and gases are used and no residues are generated. Powers of detection are comparable to other traditional methods.

  18. Analytical Model of the Nonlinear Dynamics of Cantilever Tip-Sample Surface Interactions for Various Acoustic-Atomic Force Microscopies

    NASA Technical Reports Server (NTRS)

    Cantrell, John H., Jr.; Cantrell, Sean A.

    2008-01-01

    A comprehensive analytical model of the interaction of the cantilever tip of the atomic force microscope (AFM) with the sample surface is developed that accounts for the nonlinearity of the tip-surface interaction force. The interaction is modeled as a nonlinear spring coupled at opposite ends to linear springs representing cantilever and sample surface oscillators. The model leads to a pair of coupled nonlinear differential equations that are solved analytically using a standard iteration procedure. Solutions are obtained for the phase and amplitude signals generated by various acoustic-atomic force microscope (A-AFM) techniques including force modulation microscopy, atomic force acoustic microscopy, ultrasonic force microscopy, heterodyne force microscopy, resonant difference-frequency atomic force ultrasonic microscopy (RDF-AFUM), and the commonly used intermittent contact mode (TappingMode) generally available on AFMs. The solutions are used to obtain a quantitative measure of image contrast resulting from variations in the Young modulus of the sample for the amplitude and phase images generated by the A-AFM techniques. Application of the model to RDF-AFUM and intermittent soft contact phase images of LaRC-cp2 polyimide polymer is discussed. The model predicts variations in the Young modulus of the material of 24 percent from the RDF-AFUM image and 18 percent from the intermittent soft contact image. Both predictions are in good agreement with the literature value of 21 percent obtained from independent, macroscopic measurements of sheet polymer material.

  19. Analytical computation of prompt gamma ray emission and detection for proton range verification

    NASA Astrophysics Data System (ADS)

    Sterpin, E.; Janssens, G.; Smeets, J.; Vander Stappen, François; Prieels, D.; Priegnitz, Marlen; Perali, Irene; Vynckier, S.

    2015-06-01

    A prompt gamma (PG) slit camera prototype recently demonstrated that Bragg Peak position in a clinical proton scanned beam could be measured with 1-2 mm accuracy by comparing an expected PG detection profile to a measured one. The computation of the expected PG detection profile in the context of a clinical framework is challenging but must be solved before clinical implementation. Obviously, Monte Carlo methods (MC) can simulate the expected PG profile but at prohibitively long calculation times. We implemented a much faster method that is based on analytical processing of precomputed MC data that would allow practical evaluation of this range monitoring approach in clinical conditions. Reference PG emission profiles were generated with MC simulations (PENH) in targets consisting of either 12C, 14N, 16O, 31P or 40Ca, with 10% of 1H. In a given geometry, the local PG emission can then be derived by adding the contribution of each element, according to the local energy of the proton obtained by continuous slowing down approximation and the local composition. The actual incident spot size is taken into account using an optical model fitted to measurements and by super sampling the spot with several rays (up to 113). PG transport in the patient/camera geometries and the detector response are modelled by convolving the PG production profile with a transfer function. The latter is interpolated from a database of transfer functions fitted to MC data (PENELOPE) generated for a photon source in a cylindrical phantom with various radiuses and a camera placed at various positions. As a benchmark, the analytical model was compared to MC and experiments in homogeneous and heterogeneous phantoms. Comparisons with MC were also performed in a thoracic CT. For all cases, the analytical model reproduced the prediction of the position of the Bragg peak computed with MC within 1 mm for the camera in nominal configuration. When compared to measurements, the shape of the profiles

  20. Analytical computation of prompt gamma ray emission and detection for proton range verification.

    PubMed

    Sterpin, E; Janssens, G; Smeets, J; Vander Stappen, François; Prieels, D; Priegnitz, Marlen; Perali, Irene; Vynckier, S

    2015-06-21

    A prompt gamma (PG) slit camera prototype recently demonstrated that Bragg Peak position in a clinical proton scanned beam could be measured with 1-2 mm accuracy by comparing an expected PG detection profile to a measured one. The computation of the expected PG detection profile in the context of a clinical framework is challenging but must be solved before clinical implementation. Obviously, Monte Carlo methods (MC) can simulate the expected PG profile but at prohibitively long calculation times. We implemented a much faster method that is based on analytical processing of precomputed MC data that would allow practical evaluation of this range monitoring approach in clinical conditions. Reference PG emission profiles were generated with MC simulations (PENH) in targets consisting of either (12)C, (14)N, (16)O, (31)P or (40)Ca, with 10% of (1)H. In a given geometry, the local PG emission can then be derived by adding the contribution of each element, according to the local energy of the proton obtained by continuous slowing down approximation and the local composition. The actual incident spot size is taken into account using an optical model fitted to measurements and by super sampling the spot with several rays (up to 113). PG transport in the patient/camera geometries and the detector response are modelled by convolving the PG production profile with a transfer function. The latter is interpolated from a database of transfer functions fitted to MC data (PENELOPE) generated for a photon source in a cylindrical phantom with various radiuses and a camera placed at various positions. As a benchmark, the analytical model was compared to MC and experiments in homogeneous and heterogeneous phantoms. Comparisons with MC were also performed in a thoracic CT. For all cases, the analytical model reproduced the prediction of the position of the Bragg peak computed with MC within 1 mm for the camera in nominal configuration. When compared to measurements, the shape of the

  1. Analytical computation of prompt gamma ray emission and detection for proton range verification.

    PubMed

    Sterpin, E; Janssens, G; Smeets, J; Vander Stappen, François; Prieels, D; Priegnitz, Marlen; Perali, Irene; Vynckier, S

    2015-06-21

    A prompt gamma (PG) slit camera prototype recently demonstrated that Bragg Peak position in a clinical proton scanned beam could be measured with 1-2 mm accuracy by comparing an expected PG detection profile to a measured one. The computation of the expected PG detection profile in the context of a clinical framework is challenging but must be solved before clinical implementation. Obviously, Monte Carlo methods (MC) can simulate the expected PG profile but at prohibitively long calculation times. We implemented a much faster method that is based on analytical processing of precomputed MC data that would allow practical evaluation of this range monitoring approach in clinical conditions. Reference PG emission profiles were generated with MC simulations (PENH) in targets consisting of either (12)C, (14)N, (16)O, (31)P or (40)Ca, with 10% of (1)H. In a given geometry, the local PG emission can then be derived by adding the contribution of each element, according to the local energy of the proton obtained by continuous slowing down approximation and the local composition. The actual incident spot size is taken into account using an optical model fitted to measurements and by super sampling the spot with several rays (up to 113). PG transport in the patient/camera geometries and the detector response are modelled by convolving the PG production profile with a transfer function. The latter is interpolated from a database of transfer functions fitted to MC data (PENELOPE) generated for a photon source in a cylindrical phantom with various radiuses and a camera placed at various positions. As a benchmark, the analytical model was compared to MC and experiments in homogeneous and heterogeneous phantoms. Comparisons with MC were also performed in a thoracic CT. For all cases, the analytical model reproduced the prediction of the position of the Bragg peak computed with MC within 1 mm for the camera in nominal configuration. When compared to measurements, the shape of the

  2. Analytical solutions of the time-dependent radiation force for a two-level atom interacting with a continuous-wave single-mode laser

    SciTech Connect

    Noh, Heung-Ryoul; Jhe, Wonho

    2010-09-15

    This work presents an analytical calculation of the time-dependent radiation forces on a two-level atom interacting with a single-mode laser field. Such a closed and compact expression of the radiation forces is derived by solving the optical Bloch equations analytically. It is confirmed, in particular, that the radiation force consists of reactive as well as dissipative components, whose explicit analytical forms of the temporal solutions can be explicitly obtained. The succinct analytical solutions of the radiation forces may be helpful for a convenient and intuitive description of the complex atomic dynamics such as interaction with various laser fields.

  3. Superradiant cascade emissions in an atomic ensemble via four-wave mixing

    SciTech Connect

    Jen, H.H.

    2015-09-15

    We investigate superradiant cascade emissions from an atomic ensemble driven by two-color classical fields. The correlated pair of photons (signal and idler) is generated by adiabatically driving the system with large-detuned light fields via four-wave mixing. The signal photon from the upper transition of the diamond-type atomic levels is followed by the idler one which can be superradiant due to light-induced dipole–dipole interactions. We then calculate the cooperative Lamb shift (CLS) of the idler photon, which is a cumulative effect of interaction energy. We study its dependence on a cylindrical geometry, a conventional setup in cold atom experiments, and estimate the maximum CLS which can be significant and observable. Manipulating the CLS of cascade emissions enables frequency qubits that provide alternative robust elements in quantum network. - Highlights: • Superradiance from a cascade atomic transition. • Correlated photon pair generation via four-wave mixing. • Dynamical light–matter couplings in a phased symmetrical state. • Cooperative Lamb shift in a cylindrical atomic ensemble.

  4. Application of microwave plasma atomic emission spectrometry (MP-AES) for environmental monitoring of industrially contaminated sites in Hyderabad city.

    PubMed

    Kamala C T; Balaram V; Dharmendra V; Satyanarayanan M; Subramanyam K S V; Krishnaiah A

    2014-11-01

    Recently introduced microwave plasma-atomic emission spectroscopy (MP-AES) represents yet another and very important addition to the existing array of modern instrumental analytical techniques. In this study, an attempt is made to summarize the performance characteristics of MP-AES and its potential as an analytical tool for environmental studies with some practical examples from Patancheru and Uppal industrial sectors of Hyderabad city. A range of soil, sediment, water reference materials, particulate matter, and real-life samples were chosen to evaluate the performance of this new analytical technique. Analytical wavelengths were selected considering the interference effects of other concomitant elements present in different sample solutions. The detection limits for several elements were found to be in the range from 0.05 to 5 ng/g. The trace metals analyzed in both the sectors followed the topography with more pollution in the low-lying sites. The metal contents were found to be more in ground waters than surface waters. Since a decade, the pollutants are transfered from Patancheru industrial area to Musi River. After polluting Nakkavagu and turning huge tracts of agricultural lands barren besides making people residing along the rivulet impotent and sick, industrialists of Patancheru are shifting the effluents to downstream of Musi River through an 18-km pipeline from Patancheru. Since the effluent undergoes primary treatment at Common Effluent Treatment Plant (CETP) at Patanchru and travels through pipeline and mixes with sewage, the organic effluents will be diluted. But the inorganic pollutants such as heavy and toxic metals tend to accumulate in the environmental segments near and downstreams of Musi River. The data generated by MP-AES of toxic metals like Zn, Cu, and Cr in the ground and surface waters can only be attributed to pollution from Patancheru since no other sources are available to Musi River.

  5. Statistical evaluation of an inductively coupled plasma atomic emission spectrometric method for routine water quality testing

    USGS Publications Warehouse

    Garbarino, J.R.; Jones, B.E.; Stein, G.P.

    1985-01-01

    In an interlaboratory test, inductively coupled plasma atomic emission spectrometry (ICP-AES) was compared with flame atomic absorption spectrometry and molecular absorption spectrophotometry for the determination of 17 major and trace elements in 100 filtered natural water samples. No unacceptable biases were detected. The analysis precision of ICP-AES was found to be equal to or better than alternative methods. Known-addition recovery experiments demonstrated that the ICP-AES determinations are accurate to between plus or minus 2 and plus or minus 10 percent; four-fifths of the tests yielded average recoveries of 95-105 percent, with an average relative standard deviation of about 5 percent.

  6. Ion-induced molecular emission of polymers: analytical potentialities of FTIR and mass spectroscopy

    NASA Astrophysics Data System (ADS)

    Picq, V.; Balanzat, E.

    1999-05-01

    The release of small gaseous molecules is a general phenomenon of irradiated polymers. Polyethylene (PE), polypropylene (PP) and polybutene (PB) were irradiated with ions of different electronic stopping power. We show that the gas emission can provide important information on the damage process if a reliable chemical identification of the molecules released and accurate yield values are obtained. The outgassing products were analysed by two techniques: (1) by a novel set-up using a Fourier Transform Infrared (FTIR) analysis of the gas mixture released from the polymer film and (2) by residual gas analysis (RGA) with a quadrupole mass spectrometer. Comparing the analytical potentialities of both methods we come to the conclusion that the FTIR method gives a more straightforward and accurate determination of the chemical nature and of the yield of most of the released molecules. However, RGA provides complementary information on the gas release kinetics and also on the release of heavy hydrocarbon molecules and symmetric molecules like molecular hydrogen.

  7. Model for atomic oxygen visible line emissions in Comet C/1995 O1 Hale-Bopp

    NASA Astrophysics Data System (ADS)

    Raghuram, Susarla; Bhardwaj, Anil

    2013-03-01

    We have recently developed a coupled chemistry-emission model for the green (5577 Å) and red-doublet (6300, 6364 Å) emissions of atomic oxygen on Comet C/1996 B2 Hyakutake. In the present work we applied our model to Comet C/1995 O1 Hale-Bopp, which had an order of magnitude higher H2O production rate than Comet Hyakutake, to evaluate the photochemistry associated with the production and loss of O(1S) and O(1D) atoms and emission processes of green and red-doublet lines. We present the wavelength-dependent photo-attenuation rates for different photodissociation processes forming O(1S) and O(1D). The calculated radiative efficiency profiles of O(1S) and O(1D) atoms show that in Comet Hale-Bopp the green and red-doublet emissions are emitted mostly above radial distances of 103 and 104 km, respectively. The model calculated [OI] 6300 Å emission surface brightness and average intensity over the Fabry-Pérot spectrometer field of view are consistent with the observation of Morgenthaler et al. (Morgenthaler, J.P. et al. [2001]. Astrophys. J. 563, 451-461), while the intensity ratio of green to red-doublet emission is in agreement with the observation of Zhang et al. (Zhang, H.W., Zhao, G., Hu, J.Y. [2001]. Astron. Astophys. 367 (3), 1049-1055). In Comet Hale-Bopp, for cometocentric distances less than 105 km, the intensity of [OI] 6300 Å line is mainly governed by photodissociation of H2O. Beyond 105 km, O(1D) production is dominated by photodissociation of the water photochemical daughter product OH. Whereas the [OI] 5577 Å emission line is controlled by photodissociation of both H2O and CO2. The calculated mean excess energy in various photodissociation processes show that the photodissociation of CO2 can produce O(1S) atoms with higher excess velocity compared to the photodissociation of H2O. Thus, our model calculations suggest that involvement of multiple sources in the formation of O(1S) could be a reason for the larger width of green line than that of red

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

    SciTech Connect

    Fara, M.; Novak, F.

    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).

  9. Optimization of a hydride generation metallic furnace atomic absorption spectrometry (HG-MF-AAS) method for tin determination: analytical and morphological parameters of a metallic atomizer.

    PubMed

    Moretto Galazzi, Rodrigo; Arruda, Marco Aurélio Zezzi

    2013-12-15

    The present work describes a metallic tube as hydride atomizer for atomic absorption spectrometry. Its performance is evaluated through tin determination, and the accuracy of the method assessed through the analysis of sediment and water samples. Some chemical parameters (referring to the generation of the hydride) such as acid, NaOH and THB concentrations, as well as physical parameters (referring to the transport of the hydride) such as carrier, acetylene, air flow-rates, flame composition, coil length, tube hole area, among others, are evaluated for optimization of the method. Scanning electron microscopy is used for evaluating morphological parameters in both new and used (after 150 h) tube atomizers. The method presents linear Sn concentration from 50 to 1000 µg L(-1) (r>0.9995; n=3) and the analytical frequency of ca. 40 h(-1). The limit of detection (LOD) is 7.1 µg L(-1) and the precision, expressed as RSD is less than 4% (200 µg L(-1); n=10). The accuracy is evaluated through reference materials, and the results are similar at 95% confidence level according to the t-test.

  10. Laser sampling system for an inductively-coupled atomic emission spectrometer. Final report

    SciTech Connect

    1998-02-15

    A laser sampling system was attached to a Perkin Elmer Optima 3000 inductively-coupled plasma, atomic emission spectrometer that was already installed and operating in the Chemistry and Geochemistry Department at the Colorado School of Mines. The use of the spectrometer has been highly successful. Graduate students and faculty from at least four different departments across the CSM campus have used the instrument. The final report to NSF is appended to this final report. Appendices are included which summarize several projects utilizing this instrument: acquisition of an inductively-coupled plasma atomic emission spectrometer for the geochemistry program; hydrogen damage susceptibility assessment for high strength steel weldments through advanced hydrogen content analysis, 1996 and 1997 annual reports; and methods for determination of hydrogen distribution in high strength steel welds.

  11. Analysis of the Essential Nutrient Strontium in Marine Aquariums by Atomic Absorption Spectroscopy: An Undergraduate Analytical Chemistry Laboratory Exercise

    NASA Astrophysics Data System (ADS)

    Gilles de Pelichy, Laurent D.; Adam, Carl; Smith, Eugene T.

    1997-10-01

    An undergraduate atomic absorption spectroscopy (AAS) laboratory experiment is presented involving the analysis of the essential nutrient strontium in a real-life sample, sea water. The quantitative analysis of strontium in sea water is a problem well suited for an undergraduate analytical chemistry laboratory. Sea water contains numerous components which prevent the direct quantitative determination of strontium. Students learn first hand about the role of interferences in analytical measurements, and about the method of standard addition which is used to minimize these effects. This laboratory exercise also introduces undergraduate students to practical problems associated with AAS. We encourage students as a part of this experiment to collect and analyze marine water samples from local pet shops.

  12. Mercury determination in non- and biodegradable materials by cold vapor capacitively coupled plasma microtorch atomic emission spectrometry.

    PubMed

    Frentiu, Tiberiu; Mihaltan, Alin I; Ponta, Michaela; Darvasi, Eugen; Frentiu, Maria; Cordos, Emil

    2011-10-15

    A new analytical system consisting of a low power capacitively coupled plasma microtorch (20 W, 13.56 MHz, 150 ml min(-1) Ar) and a microspectrometer was investigated for the Hg determination in non- and biodegradable materials by cold-vapor generation, using SnCl(2) reductant, and atomic emission spectrometry. The investigated miniaturized system was used for Hg determination in recyclable plastics from electronic equipments and biodegradable materials (shopping bags of 98% biodegradable polyethylene and corn starch) with the advantages of easy operation and low analysis costs. Samples were mineralized in HNO(3)-H(2)SO(4) mixture in a high-pressure microwave system. The detection limits of 0.05 ng ml(-1) or 0.08 μg g(-1) in solid sample were compared with those reported for other analytical systems. The method precision was 1.5-9.4% for Hg levels of 1.37-13.9 mg kg(-1), while recovery in two polyethylene certified reference materials in the range 98.7 ± 4.5% (95% confidence level).

  13. Comparison of Analytical Methods: Direct Emission versus First-Derivative Fluorometric Methods for Quinine Determination in Tonic Waters

    NASA Astrophysics Data System (ADS)

    Pandey, Siddharth; Borders, Tammie L.; Hernández, Carmen E.; Roy, Lindsay E.; Reddy, Gaddum D.; Martinez, Geo L.; Jackson, Autumn; Brown, Guenevere; Acree, William E., Jr.

    1999-01-01

    An undergraduate laboratory experiment is designed for the quantitative determination of quinine in tonic water samples. It is based upon direct fluorescence emission and first-derivative spectroscopic methods. Unlike other published laboratory experiments, our method exposes students to the general method of derivative spectroscopy, an important, often-used analytical technique for eliminating sample matrix and background absorbance effects and for treating overlapped spectral bands. The statistical treatment allows students to compare concentrations directly calculated from the measured fluorescence emission intensity with values obtained from the first-derivative emission spectra, to ascertain whether there is a difference between the two analytical methods. Method selection and validation are important items routinely encountered by practicing analytical chemists.

  14. Analytic expressions for Atomic Layer Deposition: coverage, throughput, and materials utilization in cross-flow, particle coating, and spatial ALD

    SciTech Connect

    Yanguas-Gil, Angel; Elam, Jeffrey W.

    2014-05-01

    In this work, the authors present analytic models for atomic layer deposition (ALD) in three common experimental configurations: cross-flow, particle coating, and spatial ALD. These models, based on the plug-flow and well-mixed approximations, allow us to determine the minimum dose times and materials utilization for all three configurations. A comparison between the three models shows that throughput and precursor utilization can each be expressed by universal equations, in which the particularity of the experimental system is contained in a single parameter related to the residence time of the precursor in the reactor. For the case of cross-flow reactors, the authors show how simple analytic expressions for the reactor saturation profiles agree well with experimental results. Consequently, the analytic model can be used to extract information about the ALD surface chemistry (e. g., the reaction probability) by comparing the analytic and experimental saturation profiles, providing a useful tool for characterizing new and existing ALD processes. (C) 2014 American Vacuum Society

  15. In situ calibration of inductively coupled plasma-atomic emission and mass spectroscopy

    DOEpatents

    Braymen, S.D.

    1996-06-11

    A method and apparatus are disclosed for in situ addition calibration of an inductively coupled plasma atomic emission spectrometer or mass spectrometer using a precision gas metering valve to introduce a volatile calibration gas of an element of interest directly into an aerosol particle stream. The present in situ calibration technique is suitable for various remote, on-site sampling systems such as laser ablation or nebulization. 5 figs.

  16. Development of source testing, analytical, and mutagenicity bioassay procedures for evaluating emissions from municipal and hospital waste combustors.

    PubMed Central

    Watts, R R; Lemieux, P M; Grote, R A; Lowans, R W; Williams, R W; Brooks, L R; Warren, S H; DeMarini, D M; Bell, D A; Lewtas, J

    1992-01-01

    Incineration is currently being used for disposal of about 10% of the solid waste generated in the United States, and this percentage will likely increase as land disposal declines. Siting new incinerators, however, is often controversial because of concerns related to the possibility of adverse health effects and environmental contamination from long-term exposure to stack emissions. Specific concerns relate to the adequacies of a) stack emission testing protocols, b) existing regulations, and c) compliance monitoring and enforcement of regulations. U.S. Environmental Protection Agency laboratories are cooperatively conducting research aimed at developing new testing equipment and procedures that will allow a more comprehensive assessment of the complex mixture of organics that is present in stack emissions. These efforts are directed specifically toward developing source testing equipment and procedures, analytical procedures, and bioassay procedures. The objectives of this study were to field test two types of high-volume source dilution samplers, collect stack samples for use in developing analytical and mutagenicity bioassay procedures, and determine mutagenicity of organics associated with emission particles from two municipal waste combustors and a hospital waste combustor. Data are presented for particle concentrations and emission rates, extractable organic concentrations and emission rates, and Salmonella (Ames) mutagenic potency and emission rates. The mutagenic emission rates and emission factors are compared to other incinerators and combustion sources. PMID:1486854

  17. Europa - Ultraviolet emissions and the possibility of atomic oxygen and hydrogen clouds

    NASA Technical Reports Server (NTRS)

    Wu, F.-M.; Judge, D. L.; Carlson, R. W.

    1978-01-01

    Emission signals from Europa with wavelength below 800 A were detected by the Pioneer 10 ultraviolet photometer. In the present paper, improved procedures for data reduction are used to determine the spatial region as well as the intensity of the suggested emission sources. The observations indicate a cloud with a radius of about 1.5 Jupiter radii and an apparent brightness of approximately 10 rayleighs for a wavelength of 500 A. It is argued that neutral oxygen atoms, along with neutral hydrogen, are produced through dissociation of water ice on the surface of Europa by particle impact. Electron impact ionization excitation of oxygen atoms in the resulting cloud then gives rise to the observed emission. The present source brightness and cloud radius results are used to estimate an oxygen column density of the order of 10 trillion per sq cm, while the density of atomic hydrogen is at most 100 billion per sq cm and 1 trillion per sq cm for molecular hydrogen.

  18. Cooperative spontaneous emission from indistinguishable atoms in arbitrary motional quantum states

    NASA Astrophysics Data System (ADS)

    Damanet, François; Braun, Daniel; Martin, John

    2016-09-01

    We investigate superradiance and subradiance of indistinguishable atoms with quantized motional states, starting with an initial total state that factorizes over the internal and external degrees of freedom of the atoms. Due to the permutational symmetry of the motional state, the cooperative spontaneous emission, governed by a recently derived master equation [F. Damanet et al., Phys. Rev. A 93, 022124 (2016), 10.1103/PhysRevA.93.022124], depends only on two decay rates γ and γ0 and a single parameter Δdd describing the dipole-dipole shifts. We solve the dynamics exactly for N =2 atoms, numerically for up to 30 atoms, and obtain the large-N limit by a mean-field approach. We find that there is a critical difference γ0-γ that depends on N beyond which superradiance is lost. We show that exact nontrivial dark states (i.e., states other than the ground state with vanishing spontaneous emission) only exist for γ =γ0 and that those states (dark when γ =γ0 ) are subradiant when γ <γ0 .

  19. Determination of Mercury in Milk by Cold Vapor Atomic Fluorescence: A Green Analytical Chemistry Laboratory Experiment

    ERIC Educational Resources Information Center

    Armenta, Sergio; de la Guardia, Miguel

    2011-01-01

    Green analytical chemistry principles were introduced to undergraduate students in a laboratory experiment focused on determining the mercury concentration in cow and goat milk. In addition to traditional goals, such as accuracy, precision, sensitivity, and limits of detection in method selection and development, attention was paid to the…

  20. The interaction of 193-nm excimer laser irradiation with single-crystal zinc oxide: Neutral atomic zinc and oxygen emission

    SciTech Connect

    Kahn, E. H.; Langford, S. C.; Dickinson, J. T.; Boatner, Lynn A

    2013-01-01

    We report mass-resolved time-of-flight measurements of neutral particles from the surface of single-crystal ZnO during pulsed 193-nm irradiation at laser fluences below the threshold for avalanche breakdown. The major species emitted are atomic Zn and O. We examine the emissions of atomic Zn as a function of laser fluence and laser exposure. Defects at the ZnO surface appear necessary for the detection of these emissions. Our results suggest that the production of defects is necessary to explain intense sustained emissions at higher fluence. Rapid, clean surface etching and high atomic zinc kinetic energies seen at higher laser fluences are also discussed.

  1. Investigation of an alternating current plasma as an element selective atomic emission detector for high-resolution capillary gas chromatography and as a source for atomic absorption and atomic emission spectrometry

    SciTech Connect

    Ombaba, J.M.

    1992-01-01

    This thesis deals with the construction and evaluation of an alternating current plasma (ACP) as an element-selective detector for high resolution capillary gas chromatography (GC) and as an excitation source for atomic absorption spectrometry (AAS) and atomic emission spectrometry (AES). The plasma, constrained in a quartz discharge tube at atmospheric pressure, is generated between two copper electrodes and utilizes helium as the plasma supporting gas. The alternating current plasma power source consists of a step-up transformer with a secondary output voltage of 14,000 V at a current of 23 mA. The chromatographic applications studied included the following: (1) the separation and selective detection of the organotin species, tributyltin chloride (TBT) and tetrabutyltin (TEBT), in environmental matrices including mussels (mytilus edullus) and sediment from Boston Harbor, industrial waste water and industrial sludge, and (2) the detection of methylcyclopentadienylmanganesetricarbonyl (MMT) and similar compounds used as gasoline additives. An ultrasonic nebulizer was utilized as a sample introduction device for aqueous solutions when the ACP was employed as an atomization source for atomic absorption spectrometry and as an excitation source for atomic emission spectrometry. Plasma diagnostic parameters studied include spatial electron number density across the discharge tube, electronic, excitation and ionization temperatures. Interference studies both in absorption and emission modes were considered. The evaluation of a computer-aided optimization program, Drylab GC, using spearmint oil and Environmental Protection Agency (EPA) standard mixture as probes is discussed. The program is used for separation optimization and prediction of gas chromatographic parameters. The program produces a relative resolution map (RRM) which guides the analyst in selecting the most favorable temperature programming rate for the separation.

  2. LASER ABLATION-INDUCTIVELY COUPLED PLASMA-ATOMIC EMISSION SPECTROSCOPY STUDY AT THE 222-S LABORATORY USING HOT-CELL GLOVE BOX PROTOTYPE SYSTEM

    SciTech Connect

    LOCKREM LL; OWENS JW; SEIDEL CM

    2009-03-26

    This report describes the installation, testing and acceptance of the Waste Treatment and Immobilization Plant procured laser ablation-inductively coupled plasma-atomic emission spectroscopy (LA-ICP-AES) system for remotely analyzing high-level waste samples in a hot cell environment. The 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.

  3. Atomic H and N emissions from High-Pressure Discharge Plasmas

    NASA Astrophysics Data System (ADS)

    Kurunczi, P.; Becker, K.

    2000-06-01

    Hollow cathode discharge plasmas in geometries where the aperture in the hollow cathode has a diameter of 0.1 mm or less (microhollow cathode discharges, MHCDs) are efficient sources of ultraviolet (UV) and vacuum ultraviolet (VUV) excimer radiation when operated at high pressures (up to atmospheric pressure). We observed intense, monochromatic H Lyman-alpha and Lyman-beta line emissions at 121.6 nm and 102.5 nm, respectively, from MHCD plasmas in high-pressure Ne with small admixtures (up to 3 Torr) of H2. The underlying processes for the emissions were identified as very efficient near-resonant energy transfer processes between Ne excimers formed in the high pressure discharge plasma and H2 leading to the dissociation of H2 and the formation of H(n=2) and H(n=3) atoms. We have now extended these studies to Ne/N2 mixtures and observed intense, monochromatic atomic N emissions at 113.4 nm and 120.0 nm. Possible mechanisms for the emission of these N lines may involve energy transfer processes between Ne excimers and metastable N2(A) molecules. Further details will be presented at the Conference.

  4. Validation of an analytical method based on the high-resolution continuum source flame atomic absorption spectrometry for the fast-sequential determination of several hazardous/priority hazardous metals in soil

    PubMed Central

    2013-01-01

    Background The aim of this paper was the validation of a new analytical method based on the high-resolution continuum source flame atomic absorption spectrometry for the fast-sequential determination of several hazardous/priority hazardous metals (Ag, Cd, Co, Cr, Cu, Ni, Pb and Zn) in soil after microwave assisted digestion in aqua regia. Determinations were performed on the ContrAA 300 (Analytik Jena) air-acetylene flame spectrometer equipped with xenon short-arc lamp as a continuum radiation source for all elements, double monochromator consisting of a prism pre-monocromator and an echelle grating monochromator, and charge coupled device as detector. For validation a method-performance study was conducted involving the establishment of the analytical performance of the new method (limits of detection and quantification, precision and accuracy). Moreover, the Bland and Altman statistical method was used in analyzing the agreement between the proposed assay and inductively coupled plasma optical emission spectrometry as standardized method for the multielemental determination in soil. Results The limits of detection in soil sample (3σ criterion) in the high-resolution continuum source flame atomic absorption spectrometry method were (mg/kg): 0.18 (Ag), 0.14 (Cd), 0.36 (Co), 0.25 (Cr), 0.09 (Cu), 1.0 (Ni), 1.4 (Pb) and 0.18 (Zn), close to those in inductively coupled plasma optical emission spectrometry: 0.12 (Ag), 0.05 (Cd), 0.15 (Co), 1.4 (Cr), 0.15 (Cu), 2.5 (Ni), 2.5 (Pb) and 0.04 (Zn). Accuracy was checked by analyzing 4 certified reference materials and a good agreement for 95% confidence interval was found in both methods, with recoveries in the range of 94–106% in atomic absorption and 97–103% in optical emission. Repeatability found by analyzing real soil samples was in the range 1.6–5.2% in atomic absorption, similar with that of 1.9–6.1% in optical emission spectrometry. The Bland and Altman method showed no statistical significant difference

  5. Thermodynamics of atomic and ionized hydrogen: analytical results versus equation-of-state tables and Monte Carlo data.

    PubMed

    Alastuey, A; Ballenegger, V

    2012-12-01

    We compute thermodynamical properties of a low-density hydrogen gas within the physical picture, in which the system is described as a quantum electron-proton plasma interacting via the Coulomb potential. Our calculations are done using the exact scaled low-temperature (SLT) expansion, which provides a rigorous extension of the well-known virial expansion-valid in the fully ionized phase-into the Saha regime where the system is partially or fully recombined into hydrogen atoms. After recalling the SLT expansion of the pressure [A. Alastuey et al., J. Stat. Phys. 130, 1119 (2008)], we obtain the SLT expansions of the chemical potential and of the internal energy, up to order exp(-|E_{H}|/kT) included (E_{H}≃-13.6 eV). Those truncated expansions describe the first five nonideal corrections to the ideal Saha law. They account exactly, up to the considered order, for all effects of interactions and thermal excitations, including the formation of bound states (atom H, ions H^{-} and H_{2}^{+}, molecule H_{2},⋯) and atom-charge and atom-atom interactions. Among the five leading corrections, three are easy to evaluate, while the remaining ones involve well-defined internal partition functions for the molecule H_{2} and ions H^{-} and H_{2}^{+}, for which no closed-form analytical formula exist currently. We provide accurate low-temperature approximations for those partition functions by using known values of rotational and vibrational energies. We compare then the predictions of the SLT expansion, for the pressure and the internal energy, with, on the one hand, the equation-of-state tables obtained within the opacity program at Livermore (OPAL) and, on the other hand, data of path integral quantum Monte Carlo (PIMC) simulations. In general, a good agreement is found. At low densities, the simple analytical SLT formulas reproduce the values of the OPAL tables up to the last digit in a large range of temperatures, while at higher densities (ρ∼10^{-2} g/cm^{3}), some

  6. [Recent Development of Atomic Spectrometry in China].

    PubMed

    Xiao, Yuan-fang; Wang, Xiao-hua; Hang, Wei

    2015-09-01

    As an important part of modern analytical techniques, atomic spectrometry occupies a decisive status in the whole analytical field. The development of atomic spectrometry also reflects the continuous reform and innovation of analytical techniques. In the past fifteen years, atomic spectrometry has experienced rapid development and been applied widely in many fields in China. This review has witnessed its development and remarkable achievements. It contains several directions of atomic spectrometry, including atomic emission spectrometry (AES), atomic absorption spectrometry (AAS), atomic fluorescence spectrometry (AFS), X-ray fluorescence spectrometry (XRF), and atomic mass spectrometry (AMS). Emphasis is put on the innovation of the detection methods and their applications in related fields, including environmental samples, biological samples, food and beverage, and geological materials, etc. There is also a brief introduction to the hyphenated techniques utilized in atomic spectrometry. Finally, the prospects of atomic spectrometry in China have been forecasted.

  7. A NONSTEADY-STATE ANALYTICAL MODEL TO PREDICT GASEOUS EMISSIONS OF VOLATILE ORGANIC COMPOUNDS FROM LANDFILLS. (R825689C072)

    EPA Science Inventory

    Abstract

    A general mathematical model is developed to predict emissions of volatile organic compounds (VOCs) from hazardous or sanitary landfills. The model is analytical in nature and includes important mechanisms occurring in unsaturated subsurface landfill environme...

  8. Limit of detection of 15{sub N} by gas-chromatography atomic emission detection: Optimization using an experimental design

    SciTech Connect

    Deruaz, D.; Bannier, A.; Pionchon, C.

    1995-08-01

    This paper deals with the optimal conditions for the detection of {sup 15}N determined using a four-factor experimental design from [2{sup 13}C,-1,3 {sup 15}N] caffeine measured with an atomic emission detector (AED) coupled to gas chromatography (GC). Owing to the capability of a photodiodes array, AED can simultaneously detect several elements using their specific emission lines within a wavelength range of 50 nm. So, the emissions of {sup 15}N and {sup 14}N are simultaneously detected at 420.17 nm and 421.46 nm respectively. Four independent experimental factors were tested (1) helium flow rate (plasma gas); (2) methane pressure (reactant gas); (3) oxygen pressure; (4) hydrogen pressure. It has been shown that these four gases had a significant influence on the analytical response of {sup 15}N. The linearity of the detection was determined using {sup 15}N amounts ranging from 1.52 pg to 19 ng under the optimal conditions obtained from the experimental design. The limit of detection was studied using different methods. The limits of detection of {sup 15}N was 1.9 pg/s according to the IUPAC method (International-Union of Pure and Applied Chemistry). The method proposed by Quimby and Sullivan gave a value of 2.3 pg/s and that of Oppenheimer gave a limit of 29 pg/s. For each determination, and internal standard: 1-isobutyl-3.7 dimethylxanthine was used. The results clearly demonstrate that GC AED is sensitive and selective enough to detect and measure {sup 15}N-labelled molecules after gas chromatographic separation.

  9. Analytically reduced form of multicenter integrals from Gaussian transforms. [in atomic and molecular physics

    NASA Technical Reports Server (NTRS)

    Straton, Jack C.

    1989-01-01

    The four-dimensional Fourier-Feynman transformations previously used in analytically reducing the general class of integrals containing multicenter products of 1s hydrogenic orbitals, Coulomb or Yukawa potentials, and plane waves, are replaced by the one-dimensional Gaussian transformation. This reduces the previously required double-diagonalization of the quadratic form of the multicenter integrals to only one diagonalization, yielding a simpler reduced form of the integral. The present work also extends the result to include all s states and pairs of states with l not equal to zero summed over the m quantum number.

  10. Investigation of an alternating current plasma as an element selective atomic emission detector for high-resolution capillary gas chromatography and as a source for atomic absorption and atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Ombaba, Jackson M.

    This thesis deals with the construction and evaluation of an alternating current plasma (ACP) as an element-selective detector for high resolution capillary gas chromatography (GC) and as an excitation source for atomic absorption spectrometry (AAS) and atomic emission spectrometry (AES). The plasma, constrained in a quartz discharge tube at atmospheric pressure, is generated between two copper electrodes and utilizes helium as the plasma supporting gas. The alternating current plasma power source consists of a step-up transformer with a secondary output voltage of 14,000 V at a current of 23 mA. The device exhibits a stable signal because the plasma is self-seeding and reignites itself every half cycle. A tesla coil is not required to commence generation of the plasma if the ac voltage applied is greater than the breakdown voltage of the plasma-supporting gas. The chromatographic applications studied included the following: (1) the separation and selective detection of the organotin species, tributyltin chloride (TBT) and tetrabutyltin (TEBT), in environmental matrices including mussels (Mvutilus edullus) and sediment from Boston Harbor, industrial waste water and industrial sludge, and (2) the detection of methylcyclopentadienyl manganesetricarbonyl (MMT) and similar compounds used as gasoline additives. An ultrasonic nebulizer (common room humidifier) was utilized as a sample introduction device for aqueous solutions when the ACP was employed as an atomization source for atomic absorption spectrometry and as an excitation source for atomic emission spectrometry. Plasma diagnostic parameters studied include spatial electron number density across the discharge tube, electronic, excitation and ionization temperatures. Interference studies both in absorption and emission modes were also considered. Figures of merits of selected elements both in absorption and emission modes are reported. The evaluation of a computer-aided optimization program, Drylab GC, using

  11. Improving the accuracy of carbon-to-hydrogen ratio determination for P, N, S, O, Cl, and Br-containing organic compounds using atomic emission detection.

    PubMed

    Chernetsova, Elena S; Revelsky, Alexander I; Durst, Dupont; Sobolevsky, Tim G; Revelsky, Igor A

    2005-05-01

    The objective of this work was to investigate the dependence of atomic emission detector C and H response on microwave-induced plasma conditions and to improve the accuracy of carbon-to-hydrogen ratio determination for trialkylphosphates, herbicides, chlorophenols, and sulfur-containing organic compounds. Compounds which differed structurally from the analytes were used as reference compounds. It was found that when the oxygen concentration in the helium was the maximum for the instrument (9%) relative errors in carbon-to-hydrogen ratio determination were 3-8%, irrespective of analyte and reference compound structure, whereas when working in the mode of operation recommended by the manufacturer of the instrument (1.5% oxygen in helium) the respective errors were 10-20% or higher. This improvement in the accuracy of carbon-to-hydrogen ratio determination was accompanied by a factor of ten decrease in sensitivity. PMID:15688154

  12. Ozone-stimulated emission due to atomic oxygen population inversions in an argon microwave plasma torch

    SciTech Connect

    Lukina, N. A.; Sergeichev, K. F.

    2008-06-15

    It is shown that, in a microwave torch discharge in an argon jet injected into an oxygen atmosphere at normal pressure, quasi-resonant energy transfer from metastable argon atoms to molecules of oxygen and ozone generated in the torch shell and, then, to oxygen atoms produced via the dissociation of molecular oxygen and ozone leads to the inverse population of metastable levels of atomic oxygen. As a result, the excited atomic oxygen with population inversions becomes a gain medium for lasing at wavelengths of 844.6 and 777.3 nm (the 3{sup 3}P-3{sup 3}S and 3{sup 5}P-3{sup 5}S transitions). It is shown that an increase in the ozone density is accompanied by an increase in both the lasing efficiency at these wavelength and the emission intensity of the plasma-forming argon at a wavelength of 811.15 nm (the {sup 2}P{sup 0}4s-{sup 2}P{sup 0}4p transition). When the torch operates unstably, the production of singlet oxygen suppresses ozone generation; as a result, the lasing effect at these wavelengths disappears.

  13. Nonthermal Optical Emission Spectrometry: Direct Atomization and Excitation of Cadmium for Highly Sensitive Determination.

    PubMed

    Cai, Yi; Zhang, Ya-Jie; Wu, De-Fu; Yu, Yong-Liang; Wang, Jian-Hua

    2016-04-19

    The low atomization and excitation capability of nonthermal microplasma, e.g., dielectric barrier discharge (DBD), has greatly hampered its potential applications for the determination of metals in solution. In the present work, an inspiring development is reported for direct atomization and excitation of cadmium in aqueous solution by DBD and facilitates highly sensitive determination. A DBD microplasma is generated on the nozzle of a pneumatic micronebulizer to focus the DBD energy on a confined space and atomize/excite metals in the spray. Meanwhile, an appropriate sample matrix and nebulization in helium further improves the atomization and excitation capability of DBD. With cadmium as a model, its emission is recorded by a CCD spectrometer at 228.8 nm. By using an 80 μL sample solution nebulized at 3 μL s(-1), a linear range of 5-1000 μg L(-1) along with a detection limit of 1.5 μg L(-1) is achieved, which is comparable to those obtained by commercial bulky inductively coupled plasma (ICP)-based instrumentations. PMID:27030025

  14. Analytical modelling of acoustic emission from buried or surface-breaking cracks under stress

    NASA Astrophysics Data System (ADS)

    Ben Khalifa, W.; Jezzine, K.; Hello, G.; Grondel, S.

    2012-03-01

    Acoustic emission (AE) is a non-destructive testing method used in various industries (aerospace, petrochemical and pressure-vessel industries in general, power generation, civil engineering, mechanical engineering, etc...) for the examination of large structures subjected to various stresses (e.g. mechanical loading).The energy released by a defect under stress (the AE phenomenon) can propagate as guided waves in thin structures or as surface Rayleigh waves in thick ones. Sensors (possibly permanently) are positioned at various locations on the structure under examination and are assumed to be sensitive to these waves. Then, post-processing tools typically based on signal processing and triangulation algorithms can be used to inverse these data, allowing one to estimate the position of the defect from which emanates the waves measured. The French Atomic Energy Commission is engaged in the development of tools for simulating AE examinations. These tools are based on specific models for the AE sources, for the propagation of guided or Rayleigh waves and for the behaviour of AE sensors. Here, the coupling of a fracture mechanics based model for AE source and surface/guided wave propagation models is achieved through an integral formulation relying on the elastodynamic reciprocity principle. As a first approximation, a simple piston-like model is used to predict the sensitivity of AE sensors. Predictions computed by our simulation tool are compared to results from the literature for validation purpose.

  15. Focused analyte spray emission apparatus and process for mass spectrometric analysis

    DOEpatents

    Roach, Patrick J.; Laskin, Julia; Laskin, Alexander

    2012-01-17

    An apparatus and process are disclosed that deliver an analyte deposited on a substrate to a mass spectrometer that provides for trace analysis of complex organic analytes. Analytes are probed using a small droplet of solvent that is formed at the junction between two capillaries. A supply capillary maintains the droplet of solvent on the substrate; a collection capillary collects analyte desorbed from the surface and emits analyte ions as a focused spray to the inlet of a mass spectrometer for analysis. The invention enables efficient separation of desorption and ionization events, providing enhanced control over transport and ionization of the analyte.

  16. CHIANTI-AN ATOMIC DATABASE FOR EMISSION LINES. XII. VERSION 7 OF THE DATABASE

    SciTech Connect

    Landi, E.; Del Zanna, G.; Mason, H. E.; Young, P. R.; Dere, K. P.

    2012-01-10

    The CHIANTI spectral code consists of an atomic database and a suite of computer programs to calculate the optically thin spectrum of astrophysical objects and carry out spectroscopic plasma diagnostics. The database includes atomic energy levels, wavelengths, radiative transition probabilities, collision excitation rate coefficients, and ionization and recombination rate coefficients, as well as data to calculate free-free, free-bound, and two-photon continuum emission. Version 7 has been released, which includes several new ions, significant updates to existing ions, as well as Chianti-Py, the implementation of CHIANTI software in the Python programming language. All data and programs are freely available at http://www.chiantidatabase.org, while the Python interface to CHIANTI can be found at http://chiantipy.sourceforge.net.

  17. Regime Transition in Electromechanical Fluid Atomization and Implications to Analyte Ionization for Mass Spectrometric Analysis

    PubMed Central

    Forbes, Thomas P.; Degertekin, F. Levent; Fedorov, Andrei G.

    2015-01-01

    The physical processes governing the transition from purely mechanical ejection to electromechanical ejection to electrospraying are investigated through complementary scaling analysis and optical visualization. Experimental characterization and visualization are performed with the ultrasonically-driven array of micromachined ultrasonic electrospray (AMUSE) ion source to decouple the electrical and mechanical fields. A new dimensionless parameter, the Fenn number, is introduced to define a transition between the spray regimes, in terms of its dependence on the characteristic Strouhal number for the ejection process. A fundamental relationship between the Fenn and Strouhal numbers is theoretically derived and confirmed experimentally in spraying liquid electrolytes of different ionic strength subjected to a varying magnitude electric field. This relationship and the basic understanding of the charged droplet generation physics have direct implications on the optimal ionization efficiency and mass spectrometric response for different types of analytes. PMID:20729096

  18. Atom-dimer scattering length for fermions with different masses: Analytical study of limiting cases

    SciTech Connect

    Alzetto, F.; Leyronas, X.; Combescot, R.

    2010-12-15

    We consider the problem of obtaining the scattering length for a fermion colliding with a dimer, formed from a fermion identical to the incident one and another different fermion. This is done in the universal regime where the range of interactions is short enough that the scattering length a for nonidentical fermions is the only relevant quantity. This is the generalization to fermions with different masses of the problem solved long ago by Skorniakov and Ter-Martirosian for particles with equal masses. We solve this problem analytically in the two limiting cases where the mass of the solitary fermion is very large or very small compared to the mass of the two other identical fermions. This is done for both the value of the scattering length and the function entering the Skorniakov-Ter-Martirosian integral equation, for which simple explicit expressions are obtained.

  19. Transition of correlated-electron emission in nonsequential double ionization of Ar atoms.

    PubMed

    Zhang, Zilong; Zhang, Jingtao; Bai, Lihua; Wang, Xu

    2015-03-23

    Emission of the two electrons released from nonsequential double ionization of argon atoms is anticorrelated at lower laser intensities but is correlated at higher laser intensities. Such a transition is caused by the momentum change of recollision-induced-ionization (RII) electrons. At lower laser intensities, the Coulomb repulsion between the two RII electrons dominates the motion of electrons and pushes them leaving the laser field back-to-back. At higher laser intensities, the drift momentum obtained from the laser field dominates the motion of electrons and drives them leaving the laser field side-by-side.

  20. Preconcentration of heavy metals in urine and quantification by inductively coupled plasma atomic emission spectrometry.

    PubMed

    López-Artíguez, M; Cameán, A; Repetto, M

    1993-01-01

    This paper describes a method for the determination of heavy metals (Co, Ni, Cu, Cd, Pb) in urine by inductively coupled plasma atomic emission spectrometry (ICP-AES). The method proposed requires purification of the samples with activated charcoal under acidic conditions before preconcentration by complexation with ammonium pyrrolidinedithiocarbamate (APDC). The formed complexes are extracted with methyl isobutyl ketone (MIBK) and the resulting residue is finally digested under acid oxidant conditions. Because of its low detection limit (below 10 micrograms/L), this procedure can be applied conveniently for toxicological diagnostic purposes. PMID:8429621

  1. Photochemistry of atomic oxygen green and red-doublet emissions in comets at larger heliocentric distances

    NASA Astrophysics Data System (ADS)

    Raghuram, Susarla; Bhardwaj, Anil

    2014-06-01

    Context. In comets, the atomic oxygen green (5577 Å) to red-doublet (6300, 6364 Å) emission intensity ratio (G/R ratio) of 0.1 has been used to confirm H2O as the parent species producing forbidden oxygen emission lines. The larger (>0.1) value of G/R ratio observed in a few comets is ascribed to the presence of higher CO2 and CO relative abundances in the cometary coma. Aims: We aim to study the effect of CO2 and CO relative abundances on the observed G/R ratio in comets observed at large (>2 au) heliocentric distances by accounting for important production and loss processes of O(1S) and O(1D) atoms in the cometary coma. Methods: Recently we have developed a coupled chemistry-emission model to study photochemistry of O(1S) and O(1D) atoms and the production of green and red-doublet emissions in comets Hyakutake and Hale-Bopp. In the present work we applied the model to six comets where green and red-doublet emissions are observed when they are beyond 2 au from the Sun. Results: The collisional quenching of O(1S) and O(1D) can alter the G/R ratio more significantly than that due to change in the relative abundances of CO2 and CO. In a water-dominated cometary coma and with significant (>10%) CO2 relative abundance, photodissociation of H2O mainly governs the red-doublet emission, whereas CO2 controls the green line emission. If a comet has equal composition of CO2 and H2O, then ~50% of red-doublet emission intensity is controlled by the photodissociation of CO2. The role of CO photodissociation is insignificant in producing both green and red-doublet emission lines and consequently in determining the G/R ratio. Involvement of multiple production sources in the O(1S) formation may be the reason for the observed higher green line width than that of red lines. The G/R ratio values and green and red-doublet line widths calculated by the model are consistent with the observation. Conclusions: Our model calculations suggest that in low gas production rate comets the G

  2. Theory of electron emission in high fields from atomically sharp emitters: Validity of the Fowler-Nordheim equation

    NASA Astrophysics Data System (ADS)

    Cutler, P. H.; He, Jun; Miller, J.; Miskovsky, N. M.; Weiss, B.; Sullivan, T. E.

    1993-04-01

    Field emission from metallic emitters is generally described by the Fowler-Nordheim [F-N] theory, which is based on a planar model of the tip with a classical image correction. Within the free electron model and the WKB approximation, the planar tip model leads to the well-known Fowler-Nordheim equation, which predicts that a plot of log J/F 2 versus 1/F, where J is the current density and F, the field, should be a straight line within the narrow range of field strengths of typical field emission experiments, 3 - 5V/nm. This has been experimentally confirmed for conventional emitters, (i.e., electrolytically etched tips with radii ⪆50 nm). Field emitters fabricated with today's new techniques are much sharper with radii of curvature of the order of nm's or even the size of a single atom. Hence, the local geometry of the tip may become an important factor in the electron emission process. To investigate the effects of the shape and/or size on emission, the authors, in a recent series of papers, studied the dependence of the current-voltage characteristics on the local geometry of pointed emitters. It was found that the calculated results, plotted as log J/V 2 vs. 1/V, do not exhibit the straight line behavior predicted by the Fowler-Nordheim theory. In addition, there is a dramatic increase in the tunneling current for a fixed external bias, V, relative to the Fowler-Nordheim result for a planar model of the tip with the same bias voltage. Using the exact current integral additional results have been obtained exhibiting the effects of emitter curvature on field electron energy distributions and on electron emission in high fields and temperatures. These results continue to differ with the predictions of the Fowler-Nordheim equation for the same emitter models. Therefore, the adequacy of a β-factor in the conventional planar model Fowler-Nordheim equation to account for emitter curvature is examined. It is demonstrated that even a β-modified Fowler

  3. Energetic Neutral Atom Emissions From Venus: VEX Observations and Theoretical Modeling

    NASA Technical Reports Server (NTRS)

    Fok, M.-C.; Galli, A.; Tanaka, T.; Moore, T. E.; Wurz, P.; Holmstrom, M.

    2007-01-01

    Venus has almost no intrinsic magnetic field to shield itself from its surrounding environment. The solar wind thus directly interacts with the planetary ionosphere and atmosphere. One of the by-products of this close encounter is the production of energetic neutral atom (ENA) emissions. Theoretical studies have shown that significant amount of ENAs are emanated from the planet. The launch of the Venus Express (VEX) in 2005 provided the first light ever of the Venus ENA emissions. The observed ENA flux level and structure are in pretty good agreement with the theoretical studies. In this paper, we present VEX ENA data and the comparison with numerical simulations. We seek to understand the solar wind interaction with the planet and the impacts on its atmospheres.

  4. PHYSICAL BASIS OF QUANTUM ELECTRONICS: Variation of the emission characteristics of an atom located near an ideally conducting conical surface

    NASA Astrophysics Data System (ADS)

    Klimov, Vasilii V.; Perventsev, Ya A.

    1999-10-01

    The line width and the emission frequency of an atom located near the vertex of an ideally conducting cone or inside a conical cavity in an ideal conductor are analysed. It is shown that the influence of the vertex diminishes with decrease in the vertex angle. On the other hand, the line width and the emission frequency of an atom located in a conical cavity may both increase and decrease greatly, depending on the position of the atom and on the vertex angle of the cavity. The results obtained may prove useful in the development of both monatomic microlasers and spectrally selective near-field nanoscopes.

  5. A device for automatic photoelectric control of the analytical gap for emission spectrographs

    USGS Publications Warehouse

    Dietrich, John A.; Cooley, Elmo F.; Curry, Kenneth J.

    1977-01-01

    A photoelectric device has been built that automatically controls the analytical gap between electrodes during excitation period. The control device allows for precise control of the analytical gap during the arcing process of samples, resulting in better precision of analysis.

  6. Electrospray mass spectrometry with controlled in-source atomization (ERIAD) as a promising elemental method: evaluation of analytical features.

    PubMed

    Gall, L N; Fomina, N S; Giles, R; Masukevich, S V; Beliaeva, O A; Gall, N R

    2015-01-01

    Electrospray ionization with controlled in-source fragmentation and atomization (ERIAD) is promising method for mass-spectrometric elemental analysis. This paper concerns the main analytical features and necessary instrumentation for ERIAD. The method is shown to be effective for more than 70 elements of the periodic table: those that present as cations in a water solution. It shows a high absolute sensitivity with a low spread from Li to U, and a detection limit of tens of parts per trillion. The soft ionization used results in the absence of plasma chemical reaction products, typical for inductively coupled plasma mass spectrometry, and the spectra are nearly free from interferences. The method does not require a high resolution and can be used for samples with an artificial isotopic content. The method is essentially valid for radiochemistry and metallomics, as it has the possibility to combine measurements of chemical, elemental, and even isotopic content simultaneously. PMID:26307716

  7. Laser excited analytical atomic and ionic fluorescence in flames, furnaces and inductively coupled plasmas—I. General considerations

    NASA Astrophysics Data System (ADS)

    Omenetto, N.; Human, H. G. C.

    Several important parameters for the analytical use of laser excited fluorescence spectrometry in flames, graphite furnaces and inductively coupled plasmas are discussed in some detail. These parameters include the laser characteristics such as peak power, pulse duration, spectral bandwidth and repetition rate, the choice of the excitation line, the optical arrangement and the detection system, this last one centred on the widespread use of the boxcar averager. It is shown that, if the ultimate sensitivity is the goal to be achieved, then the choice must be the electrothermal atomization. However, even for flames and inductively coupled plasmas, excellent results are possible provided that: (i) the laser system allows complete spectral coverage in the ultraviolet: (ii) saturation of the fluorescence signal can be approached over a large sample volume; and (iii) the gated detection parameters and the laser repetition frequency are optimized with respect to each other so as to reach the maximum signal-to-noise ratio.

  8. Hybrid Modeling of Hydrogen Energetic Neutral Atoms from Mars: Emission from Subsolar Magnetosheath

    NASA Astrophysics Data System (ADS)

    Wang, Xiao-Dong; Kallio, Esa; Barabash, Stas; Futaana, Yoshifumi

    2015-04-01

    We simulated the hydrogen energetic neutral atom (ENA) emission from the subsolar magnetosheath of Mars using a hybrid scheme in order to reproduce multiple features of the statistical features obtained from statistical observations of the Neutral Particle Detectors on the Mars Express spacecraft. We track the charge exchange reaction between the ions produced by the hybrid plasma model under a Martian neutral exosphere model. The simulation exhibits a directional emission of hydrogen ENAs from dayside magnetosheath. Particularly, the stronger ENA emission in the opposite direction of the solar wind convection electric field is reproduced, being consistent with the observations, by a corresponding asymmetry in the proton flux at the lower magnetosheath. This proton flux asymmetry is caused by the mass loading of ionospheric heavy ions in the direction of the convection electric field. We also investigate the influences of the upstream solar wind dynamic pressure. We demonstrate that higher dynamic pressure causes stronger and more anisotropic ENA emission, besides the influence of the proton flux. This dependence suggests that the induced magnetic boundary is lower during higher dynamic pressure, where the sheath protons can access to a denser exosphere and thus the charge exchange rate is higher.

  9. Comparison of four analytical techniques based on atomic spectrometry for the determination of total tin in canned foodstuffs.

    PubMed

    Boutakhrit, K; Crisci, M; Bolle, F; Van Loco, J

    2011-02-01

    Different techniques for the determination of total tin in beverages and canned foods by atomic spectrometry were compared. The performance characteristics of inductively coupled plasma-mass spectrometry (ICP-MS), hydride generation-inductively coupled plasma-atomic emission spectrometry (HG-ICP-AES), electrothermal atomisation-atomic absorption spectrometry (ETA-AAS) and inductively coupled plasma-atomic emission spectrometry (ICP-AES) were determined in terms of linearity, precision, recovery, limit of detection, decision limit (CCα) and detection capability (CCβ) (Decision 2002/657/EC). Calibration ranges were covered from ng l⁻¹ to mg l⁻¹ level. Limits of detection that ranged from 0.01, 0.05, 2.0 to 200 µg l⁻¹ were reached for ICP-MS; HG-ICP-AES; ETA-AAS and ICP-AES, respectively. Precision, calculated according to ISO 5725-2 for repeatability and within-laboratory reproducibility and expressed as relative standard deviation (RSD), ranged from 1.6% to 4.9%; and recovery, based on Decision 2002/657/EC, was found to be between 95% and 110%. Procedures for the mineralisation or extraction of total tin were compared. Wet digestion, sequentially, with nitric acid and hydrogen peroxide provided the best results. The influence of possible interferences present in canned food and beverage was studied, but no interference in the determination of tin was observed. Since maximum levels for tin established by European Union legislation vary from 50 mg kg⁻¹ in canned baby foods and infant foods up to 200 mg kg⁻¹ in canned food, ICP-AES was chosen as the preferred technique for routine analysis thanks to its good precision, reliability and ease of use. The accuracy of this routine method was confirmed by participation in six proficiency test schemes with z-scores ranging from -1.9 to 0.6. Several canned foodstuffs and beverage samples from a local market were analysed with this technique.

  10. Pressurized liquid extraction followed by gas chromatography with atomic emission detection for the determination of fenbutatin oxide in soil samples.

    PubMed

    Canosa, P; Montes, R; Lamas, J P; García-López, M; Orriols, I; Rodríguez, I

    2009-08-15

    A novel method for the determination of the miticide bis[tris(2-methyl-2-phenylpropyl)tin] oxide, also known as fenbutatin oxide (FBTO), in agricultural soils is presented. Pressurized liquid extraction (PLE) followed by analyte derivatization and extraction into isooctane was the used sample preparation approach. Selective determination was achieved by gas chromatography with atomic emission detection (GC-AED). Influence of different parameters on the performance of the extraction process is thoroughly discussed; moreover, some relevant aspects related to derivatization, determination and quantification steps are also presented. As regards PLE, the type of solvent and the temperature were the most relevant variables. Under optimized conditions, acetone, without any acidic modifier, was employed as extractant at 80 degrees C. Cells were pressurized at 1500 psi, and 2 static cycles of 1 min each were applied. Acetone extracts (ca. 25 mL) were concentrated to 1 mL, derivatized with sodium tetraethyl borate (NaBEt(4)) and the FBTO derivative, resulting from cleavage of the Sn-O-Sn bond followed by ethylation of the hydroxyl fragments, extracted into isooctane and determined by GC-AED. Under final working conditions, the proposed method provided recoveries from 76 to 99% for spiked soil samples, a limit of quantification of 2 ng g(-1) and an acceptable precision. Analysis of samples from vineyards sprayed with FBTO, confirmed the persistence of the miticide in soil for more than 1 year after being applied.

  11. NEW METHOD FOR REMOVAL OF SPECTRAL INTERFERENCES FOR BERYLLIUM ASSAY USING INDUCTIVELY COUPLED PLASMA ATOMIC EMISSION SPECTROMETRY

    SciTech Connect

    Maxwell, S; Matthew Nelson, M; Linda Youmans, L; Maureen Bernard, M

    2008-01-14

    Beryllium has been used widely in specific areas of nuclear technology. Frequent monitoring of air and possible contaminated surfaces in U.S Department of Energy (DOE) facilities is required to identify potential health risks and to protect DOE workers from beryllium-contaminated dust. A new method has been developed to rapidly remove spectral interferences prior to beryllium (Be) measurement by inductively-coupled plasma atomic emission spectrometry (ICP-AES). The ion exchange separation removes uranium (U), thorium (Th), niobium (Nb), vanadium (V), molybdenum (Mo), zirconium (Zr), tungsten (W), iron (Fe), chromium (Cr), cerium (Ce), erbium (Er) and titanium (Ti). A stacked column consisting of Diphonix Resin{reg_sign} and TEVA Resin{reg_sign} reduces the levels of the spectral interferences so that low level Be measurements can be performed accurately. If necessary, an additional anion exchange separation can be used for further removal of interferences, particularly chromium. The method has been tested using spiked filters, spiked wipe samples and certified reference material standards with high levels of interferences added. The method provides very efficient removal of spectral interferences with very good accuracy and precision for beryllium on filters or wipes. A vacuum box system is employed to reduce analytical time and reduce labor costs.

  12. Nondestructive atomic compositional analysis of BeMgZnO quaternary alloys using ion beam analytical techniques

    NASA Astrophysics Data System (ADS)

    Zolnai, Z.; Toporkov, M.; Volk, J.; Demchenko, D. O.; Okur, S.; Szabó, Z.; Özgür, Ü.; Morkoç, H.; Avrutin, V.; Kótai, E.

    2015-02-01

    The atomic composition with less than 1-2 atom% uncertainty was measured in ternary BeZnO and quaternary BeMgZnO alloys using a combination of nondestructive Rutherford backscattering spectrometry with 1 MeV He+ analyzing ion beam and non-Rutherford elastic backscattering experiments with 2.53 MeV energy protons. An enhancement factor of 60 in the cross-section of Be for protons has been achieved to monitor Be atomic concentrations. Usually the quantitative analysis of BeZnO and BeMgZnO systems is challenging due to difficulties with appropriate experimental tools for the detection of the light Be element with satisfactory accuracy. As it is shown, our applied ion beam technique, supported with the detailed simulation of ion stopping, backscattering, and detection processes allows of quantitative depth profiling and compositional analysis of wurtzite BeZnO/ZnO/sapphire and BeMgZnO/ZnO/sapphire layer structures with low uncertainty for both Be and Mg. In addition, the excitonic bandgaps of the layers were deduced from optical transmittance measurements. To augment the measured compositions and bandgaps of BeO and MgO co-alloyed ZnO layers, hybrid density functional bandgap calculations were performed with varying the Be and Mg contents. The theoretical vs. experimental bandgaps show linear correlation in the entire bandgap range studied from 3.26 eV to 4.62 eV. The analytical method employed should help facilitate bandgap engineering for potential applications, such as solar blind UV photodetectors and heterostructures for UV emitters and intersubband devices.

  13. Carbon-, sulfur-, and phosphorus-based charge transfer reactions in inductively coupled plasma-atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Grindlay, Guillermo; Gras, Luis; Mora, Juan; de Loos-Vollebregt, Margaretha T. C.

    2016-01-01

    In this work, the influence of carbon-, sulfur-, and phosphorus-based charge transfer reactions on the emission signal of 34 elements (Ag, Al, As, Au, B, Ba, Be, Ca, Cd, Co, Cr, Cu, Fe, Ga, Hg, I, In, Ir, K, Li, Mg, Mn, Na, Ni, P, Pb, Pd, Pt, S, Sb, Se, Sr, Te, and Zn) in axially viewed inductively coupled plasma-atomic emission spectrometry has been investigated. To this end, atomic and ionic emission signals for diluted glycerol, sulfuric acid, and phosphoric acid solutions were registered and results were compared to those obtained for a 1% w w- 1 nitric acid solution. Experimental results show that the emission intensities of As, Se, and Te atomic lines are enhanced by charge transfer from carbon, sulfur, and phosphorus ions. Iodine and P atomic emission is enhanced by carbon- and sulfur-based charge transfer whereas the Hg atomic emission signal is enhanced only by carbon. Though signal enhancement due to charge transfer reactions is also expected for ionic emission lines of the above-mentioned elements, no experimental evidence has been found with the exception of Hg ionic lines operating carbon solutions. The effect of carbon, sulfur, and phosphorus charge transfer reactions on atomic emission depends on (i) wavelength characteristics. In general, signal enhancement is more pronounced for electronic transitions involving the highest upper energy levels; (ii) plasma experimental conditions. The use of robust conditions (i.e. high r.f. power and lower nebulizer gas flow rates) improves carbon, sulfur, and phosphorus ionization in the plasma and, hence, signal enhancement; and (iii) the presence of other concomitants (e.g. K or Ca). Easily ionizable elements reduce ionization in the plasma and consequently reduce signal enhancement due to charge transfer reactions.

  14. Characterization of the atomic emission in inconel 718 alloy metal vapor arcs

    SciTech Connect

    Williamson, R.L.; Peebles, H.C.; Bertram, L.A.; Hareland, W.A.; Zanner, F.J.

    1986-01-01

    Visible and uv emission spectroscopy was used to identify and study various atomic species in the plasma of a vacuum arc furnace during a remelt of Inconel 718. The studies were carried out at a base pressure of 10 mtorr, and with the furnace backfilled with CO to a total pressure of 100 mtorr. Various emitting species were identified, and the internal energy distributions of a number of these species were mapped out using Boltzmann plots. Internal temperatures of 6000 to 7000/sup 0/K were measured for the neutral atomic species in the low pressure arc, while a value of 11,600/sup 0/K was obtained for the ion temperature. In addition, the density of the highly volatile element Mn in the interelectrode region was found to be greatly enhanced compared to its relative abundance in the bulk alloy, indicating the importance of vaporization in determining the atomic composition of the arc plasma. Increasing the furnace pressure resulted in an increase in the temperature of the neutral species of 1500 to 4000/sup 0/K, and an apparent suppression of the Mn vaporization rate.

  15. Electron emission in collisions of fast highly charged bare ions with helium atoms

    NASA Astrophysics Data System (ADS)

    Mondal, Abhoy; Mandal, Chittranjan; Purkait, Malay

    2016-01-01

    We have studied the electron emission from ground state helium atom in collision with fast bare heavy ions at intermediate and high incident energies. In the present study, we have applied the present three-body formalism of the three Coulomb wave (3C-3B) model and the previously adopted four-body formalism of the three Coulomb wave (3C-4B). To represent the active electron in the helium atom in the 3C-3B model, the initial bound state wavefunction is chosen to be hydrogenic with an effective nuclear charge. The wavefunction for the ejected electron in the exit channel has been approximated to be a Coulomb continuum wavefunction with same effective nuclear charge. Effectively the continuum-continuum correlation effect has been considered in the present investigation. Here we have calculated the energy and angular distribution of double differential cross sections (DDCS) at low and high energy electron emission from helium atom. The large forward-backward asymmetry is observed in the angular distribution which is explained in terms of the two-center effect (TCE). Our theoretical results are compared with available experimental results as well as other theoretical calculations based on the plain wave Born approximation (PWBA), continuum-distorted wave (CDW) approximation, continuum-distorted wave eikonal-initial state (CDW-EIS) approximation, and the corresponding values obtained from the 3C-4B model [S. Jana, R. Samanta, M. Purkait, Phys. Scr. 88, 055301 (2013)] respectively. It is observed that the four-body version of the present investigation produces results which are in better agreement with experimental observations for all cases.

  16. Consistency of atomic data for the interpretation of beam emission spectra

    NASA Astrophysics Data System (ADS)

    Delabie, E.; Brix, M.; Giroud, C.; Jaspers, R. J. E.; Marchuk, O.; O'Mullane, M. G.; Ralchenko, Yu; Surrey, E.; von Hellermann, M. G.; Zastrow, K. D.; Contributors, JET-EFDA

    2010-12-01

    Several collisional-radiative (CR) models (Anderson et al 2000 Plasma Phys. Control. Fusion 42 781-806, Hutchinson 2002 Plasma Phys. Control. Fusion 44 71-82, Marchuk et al 2008 Rev. Sci. Instrum. 79 10F532) have been developed to calculate the attenuation and the population of excited states of hydrogen or deuterium beams injected into tokamak plasmas. The datasets generated by these CR models are needed for the modelling of beam ion deposition and (excited) beam densities in current experiments, and the reliability of these data will be crucial to obtain helium ash densities on ITER combining charge exchange and beam emission spectroscopy. Good agreement between the different CR models for the neutral beam (NB) is found, if corrections to the fundamental cross sections are taken into account. First the Hα and Hβ beam emission spectra from JET are compared with the expected intensities. Second, the line ratios within the Stark multiplet are compared with the predictions of a sublevel resolved model. The measured intensity of the full multiplet is ≈30% lower than expected on the basis of beam attenuation codes and the updated beam emission rates, but apart from the atomic data this could also be due to the characterization of the NB path and line of sight integration and the absolute calibration of the optics. The modelled n = 3 to n = 4 population agrees very well with the ratio of the measured Hα to Hβ beam emission intensities. Good agreement is found as well between the NB power fractions measured with beam emission in plasma and on the JET Neutral Beam Test Bed. The Stark line ratios and σ/π intensity ratio deviate from a statistical distribution, in agreement with the CR model in parabolic states from Marchuk et al (2010 J. Phys. B: At. Mol. Opt. Phys. 43 011002).

  17. COMPARISON OF ANALYTICAL TECHNIQUES FOR MEASURING HYDROCARBON EMISSIONS FROM THE MANUFACTURE OF FIBERGLASS-REINFORCED PLASTICS

    EPA Science Inventory

    The paper discusses several projects to measure hydrocarbon emissions associated with the manufacture of fiberglass-reinforced plastics. The main purpose of the projects was to evaluate pollution prevention techniques to reduce emissions by altering raw materials, application equ...

  18. The emission of oxygen green line and density of O atom determined by using ISUAL and SABER measurements

    NASA Astrophysics Data System (ADS)

    Gao, H.; Nee, J.-B.; Xu, J.

    2012-04-01

    Emissions of the 557.7 nm green line airglow observed by the ISUAL (Imager of Sprites and Upper Atmospheric Lightning) instrument on board the FORMOSAT-2 satellite in May and November 2008 are studied here to derive the density distributions of the atomic oxygen by using atmospheric parameters from MSISE-00 model and TIMED (Thermosphere Ionosphere Mesosphere Energetics and Dynamics)/SABER (Sounding of the Atmosphere using Broadband Emission Radiometry) measurements. The May observations were made in 10 days from a fixed orbit of longitude (100° E) with the results showing emission rate and O atom density both peaked at heights of about 90 km over 10° to 20° latitudes in the Northern Hemisphere (NH). In the Southern Hemisphere (SH), the emission rate and density of O atom are both low compared with those in NH. In November, the observations were made as the satellite traveled over all 14 orbits around the earth, covering all longitudes and latitudes of 25° S-45° N. Strong peaks of emission rates and O atoms are found at heights of about 95 km in the mid-latitudes in both hemispheres. In the equator, the airglow layer has a weaker emission rate but with higher altitude compared with those of mid-latitudes. In the lower and upper mesosphere at heights below 85 km and above 105 km, there are more O atoms in the equatorial regions than in the mid-latitudes. And there is a good correlation between the O atom and the temperature structure. A comparison with O atom distribution derived from OH airglow observed by TIMED/SABER at about the same time shows similar results.

  19. Emission of hydrogen energetic neutral atoms from the Martian subsolar magnetosheath

    NASA Astrophysics Data System (ADS)

    Wang, X.-D.; Alho, M.; Jarvinen, R.; Kallio, E.; Barabash, S.; Futaana, Y.

    2016-01-01

    We have simulated the hydrogen energetic neutral atom (ENA) emissions from the subsolar magnetosheath of Mars using a hybrid model of the proton plasma charge exchanging with the Martian exosphere to study statistical features revealed from the observations of the Neutral Particle Detectors on Mars Express. The simulations reproduce well the observed enhancement of the hydrogen ENA emissions from the dayside magnetosheath in directions perpendicular to the Sun-Mars line. Our results show that the neutralized protons from the shocked solar wind are the dominant ENA population rather than those originating from the pickup planetary ions. The simulation also suggests that the observed stronger ENA emissions in the direction opposite to the solar wind convective electric field result from a stronger proton flux in the same direction at the lower magnetosheath; i.e., the proton fluxes in the magnetosheath are not cylindrically symmetric. We also confirm the observed increasing of the ENA fluxes with the solar wind dynamical pressure in the simulations. This feature is associated with a low altitude of the induced magnetic boundary when the dynamic pressure is high and the magnetosheath protons can reach to a denser exosphere, and thus, the charge exchange rate becomes higher. Overall, the analysis suggests that kinetic effects play an important and pronounced role in the morphology of the hydrogen ENA distribution and the plasma environment at Mars, in general.

  20. 14 CFR 34.82 - Sampling and analytical procedures for measuring smoke exhaust emissions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ..., DEPARTMENT OF TRANSPORTATION AIRCRAFT FUEL VENTING AND EXHAUST EMISSION REQUIREMENTS FOR TURBINE ENGINE POWERED AIRPLANES Test Procedures for Engine Smoke Emissions (Aircraft Gas Turbine Engines) § 34.82..., Environmental Protection, Volume II, Aircraft Engine Emissions, Second Edition, July 1993, effective July...

  1. A new analytical inversion method for determining regional and global emissions of greenhouse gases: sensitivity studies and application to halocarbons

    NASA Astrophysics Data System (ADS)

    Stohl, A.; Seibert, P.; Arduini, J.; Eckhardt, S.; Fraser, P.; Greally, B. R.; Maione, M.; O'Doherty, S.; Prinn, R. G.; Reimann, S.; Saito, T.; Schmidbauer, N.; Simmonds, P. G.; Vollmer, M. K.; Weiss, R. F.; Yokouchi, Y.

    2008-11-01

    A new analytical inversion method has been developed to determine the regional and global emissions of long-lived atmospheric trace gases. It exploits in situ measurement data from a global network and builds on backward simulations with a Lagrangian particle dispersion model. The emission information is extracted from the observed concentration increases over a baseline that is itself objectively determined by the inversion algorithm. The method was applied to two hydrofluorocarbons (HFC-134a, HFC-152a) and a hydrochlorofluorocarbon (HCFC-22) for the period January 2005 until March 2007. Detailed sensitivity studies with synthetic as well as with real measurement data were done to quantify the influence on the results of the a priori emissions and their uncertainties as well as of the observation and model errors. It was found that the global a posteriori emissions of HFC-134a, HFC-152a and HCFC-22 all increased from 2005 to 2006. Large increases (21%, 16%, 18%, respectively) from 2005 to 2006 were found for China, whereas the emission changes in North America and Europe were modest. For Europe, the a posteriori emissions of HFC-134a and HFC-152a were slightly higher than the a priori emissions reported to the United Nations Framework Convention on Climate Change (UNFCCC). For HCFC-22, the a posteriori emissions for Europe were substantially (by almost a factor 2) higher than the a priori emissions used, which were based on HCFC consumption data reported to the United Nations Environment Programme (UNEP). Combined with the reported strongly decreasing HCFC consumption in Europe, this suggests a substantial time lag between the reported timing of the HCFC-22 consumption and the actual timing of the HCFC-22 emission. Conversely, in China where HCFC consumption is increasing rapidly according to the UNEP data, the a posteriori emissions are only about 40% of the a priori emissions. This reveals a substantial storage of HCFC-22 and potential for future emissions in

  2. An analytical inversion method for determining regional and global emissions of greenhouse gases: Sensitivity studies and application to halocarbons

    NASA Astrophysics Data System (ADS)

    Stohl, A.; Seibert, P.; Arduini, J.; Eckhardt, S.; Fraser, P.; Greally, B. R.; Lunder, C.; Maione, M.; Mühle, J.; O'Doherty, S.; Prinn, R. G.; Reimann, S.; Saito, T.; Schmidbauer, N.; Simmonds, P. G.; Vollmer, M. K.; Weiss, R. F.; Yokouchi, Y.

    2009-03-01

    A new analytical inversion method has been developed to determine the regional and global emissions of long-lived atmospheric trace gases. It exploits in situ measurement data from three global networks and builds on backward simulations with a Lagrangian particle dispersion model. The emission information is extracted from the observed concentration increases over a baseline that is itself objectively determined by the inversion algorithm. The method was applied to two hydrofluorocarbons (HFC-134a, HFC-152a) and a hydrochlorofluorocarbon (HCFC-22) for the period January 2005 until March 2007. Detailed sensitivity studies with synthetic as well as with real measurement data were done to quantify the influence on the results of the a priori emissions and their uncertainties as well as of the observation and model errors. It was found that the global a posteriori emissions of HFC-134a, HFC-152a and HCFC-22 all increased from 2005 to 2006. Large increases (21%, 16%, 18%, respectively) from 2005 to 2006 were found for China, whereas the emission changes in North America (-9%, 23%, 17%, respectively) and Europe (11%, 11%, -4%, respectively) were mostly smaller and less systematic. For Europe, the a posteriori emissions of HFC-134a and HFC-152a were slightly higher than the a priori emissions reported to the United Nations Framework Convention on Climate Change (UNFCCC). For HCFC-22, the a posteriori emissions for Europe were substantially (by almost a factor 2) higher than the a priori emissions used, which were based on HCFC consumption data reported to the United Nations Environment Programme (UNEP). Combined with the reported strongly decreasing HCFC consumption in Europe, this suggests a substantial time lag between the reported time of the HCFC-22 consumption and the actual time of the HCFC-22 emission. Conversely, in China where HCFC consumption is increasing rapidly according to the UNEP data, the a posteriori emissions are only about 40% of the a priori

  3. Effects of liquid chromatography mobile phases and buffer salts on phosphorus inductively coupled plasma atomic emission and mass spectrometries utilizing ultrasonic nebulization and membrane desolvation.

    PubMed

    Carr, John E; Kwok, Kaho; Webster, Gregory K; Carnahan, Jon W

    2006-01-23

    Atomic spectrometry, specifically inductively coupled plasma atomic emission spectrometry (ICP-AES) and mass spectrometry (ICP-MS) show promise for heteroatom-based detection of pharmaceutical compounds. The combination of ultrasonic nebulization (USN) with membrane desolvation (MD) greatly enhances detection limits with these approaches. Because pharmaceutical analyses often incorporate liquid chromatography, the study herein was performed to examine the effects of solvent composition on the analytical behaviors of these approaches. The target analyte was phosphorus, introduced as phosphomycin. AES response was examined at the 253.7 nm atom line and mass 31 ions were monitored for the MS experiments. With pure aqueous solutions, detection limits of 5 ppb (0.5 ng in 0.1 mL injection volumes) were obtained with ICP-MS. The ICP-AES detection limit was 150 ppb. Solvent compositions were varied from 0 to 80% organic (acetonitrile and methanol) with nine buffers at concentrations typically used in liquid chromatography. In general, solvents and buffers had statistically significant, albeit small, effects on ICP-AES sensitivities. A few exceptions occurred in cases where typical liquid chromatography buffer concentrations produced higher mass loadings on the plasma. Indications are that isocratic separations can be reliably performed. Within reasonable accuracy tolerances, it appears that gradient chromatography can be performed without the need for signal response normalization. Organic solvent and buffer effects were more significant with ICP-MS. Sensitivities varied significantly with different buffers and organic solvent content. In these cases, gradient chromatography will require careful analytical calibration as solvent and buffer content is varied. However, for most buffer and solvent combinations, signal and detection limits are only moderately affected. Isocratic separations and detection are feasible.

  4. Combustor exhaust-emissions and blowout-limits with diesel number 2 and jet A fuels utilizing air-atomizing and pressure atomizing nozzles

    NASA Technical Reports Server (NTRS)

    Ingebo, R. D.; Norgren, C. T.

    1975-01-01

    Experimental tests with diesel number 2 and Jet A fuels were conducted in a combustor segment to obtain comparative data on exhaust emissions and blowout limits. An air-atomizing nozzle was used to inject the fuels. Tests were also made with diesel number 2 fuel using a pressure-atomizing nozzle to determine the effectiveness of the air-atomizing nozzle in reducing exhaust emissions. Test conditions included fuel-air ratios of 0.008 to 0.018, inlet-air total pressures and temperatures of 41 to 203 newtons per square centimeter and 477 to 811 K, respectively, and a reference velocity of 21.3 meters per second. Smoke number and unburned hydrocarbons were twice as high with diesel number 2 as with Jet A fuel. This was attributed to diesel number 2 having a higher concentration of aromatics and lower volatility than Jet A fuel. Oxides of nitrogen, carbon monoxide, and blowout limits were approximately the same for the two fuels. The air-atomizing nozzle, as compared with the pressure-atomizing nozzle, reduced oxides-of-nitrogen by 20 percent, smoke number by 30 percent, carbon monoxide by 70 percent, and unburned hydrocarbons by 50 percent when used with diesel number 2 fuel.

  5. Validation of an analytical method for the determination of cadmium (Cd) in fish by atomic absorption spectrometry with electrothermal atomisation.

    PubMed

    Costa, L C S M; Neto, A P N; Araújo, M Q; Melo, M C C; Furtado, D M S; Kikuchi, A N S

    2012-01-01

    The validation of an analytical method was carried out for the determination of cadmium (Cd) in fish. The method was based on sample digestion in a microwave oven and subsequent reading using an atomic absorption spectrometer with a graphite furnace. The factorial design of experiments was applied to assess method ruggedness using the methodology of Box et al. [Box GEP, Hunter WG, Hunter JS. 1978. Statistics for experiments: an introduction to design, data analysis and model building. New York (NY): Wiley], studying the influence of sample mass, volume and concentration of acid used for sample digestion and the volume of modifier used. To study the possible matrix effect in the determination of Cd, the standard addition method was also performed. The results were treated using the OLS method. For the normality test a homoskedastic distribution was observed for the developed method and the results were adjusted to the statistical model proposed. F-tests and Student's t-tests indicated that there was no matrix effect on the calibration curve between the concentration range 1.0-10.0 µg Cd l(-1). Parameters such as selectivity, precision, decision limit, detection capability and limit of quantification were established by the method of standard addition to blank samples. The limit of quantification was 6.8 µg kg(-1). Accuracy, which was evaluated by using a certified reference material, was 107.0%. The recovery of the spiked analyte was 93.69% for the concentration of 50 µg kg(-1). Precision was defined by the coefficient of variation observed (Horrat value), estimated in terms of repeatability and reproducibility, and the values were below the limit, which is 2.0. The validation procedure confirmed the suitability of the method.

  6. Simple analytical embedded-atom-potential model including a long-range force for fcc metals and their alloys

    NASA Astrophysics Data System (ADS)

    Cai, J.; Ye, Y. Y.

    1996-09-01

    A simple analytical embedded-atom method (EAM) model is developed. The model includes a long-range force. In this model, the electron-density function is taken as a decreasing exponential function, the two-body potential is defined as a function like a form given by Rose et al. [Phys. Rev. B 33, 7983 (1986)], and the embedding energy is assumed to be an universal form recently suggested by Banerjea and Smith. The embedding energy has a positive curvature. The model is applied to seven fcc metals (Al, Ag, Au, Cu, Ni, Pd, and Pt) and their binary alloys. All the considered properties, whether for pure metal systems or for alloy systems, are predicted to be satisfactory at least qualitatively. The model resolves the problems of Johnson's model for predicting the properties of the alloys involving metal Pd. However, more importantly, (i) by investigating the structure stability of seven fcc metals using the present model, we found that the stability energy is dominated by both the embedding energy and the pair potential for fcc-bcc stability while the pair potential dominates and is underestimated for fcc-hcp stability; and (ii) we find that the predicted total energy as a function of lattice parameter is in good agreement with the equation of state of Rose et al. for all seven fcc metals, and that this agreement is closely related to the electron density, i.e., the lower the contribution from atoms of the second-nearest neighbor to host density, the better the agreement becomes. We conclude the following: (i) for an EAM, where angle force is not considered, the long-range force is necessary for a prediction of the structure stability; or (ii) the dependence of the electron density on angle should be considered so as to improve the structure-stability energy. The conclusions are valid for all EAM models where an angle force is not considered.

  7. Measurement of lanthanum and technetium in uranium fuels by inductively coupled plasma atomic emission spectroscopy.

    SciTech Connect

    Carney, K.; Crane, P.; Cummings, D.; Krsul, J.; McKnight, R.

    1999-06-10

    An important parameter in characterizing an irradiated nuclear fuel is determining the amount of uranium fissioned. By determining the amount of uranium fissioned in the fuel a burnup performance parameter can be calculated, and the amount of fission products left in the fuel can be predicted. The quantity of uranium fissioned can be calculated from the amount of lanthanum and technetium present in the fuel. Lanthanum and technetium were measured in irradiated fuel samples using an Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) instrument and separation equipment located in a shielded glove-box. A discussion of the method, interferences, detection limits, quality control and a comparison to other work will be presented.

  8. The application of atomic emission spectroscopy to chromatographic analyses for element-selective detection

    SciTech Connect

    Seeley, J.A.

    1992-01-01

    The goal of this work was to investigate the properties of existing atomic emission systems which are useful for element-selective detection of chromatographic effluent. A microwave induced plasma (MIP) system has been optimized for the selective detection of boron in the effluent of a gas chromatograph. A method was developed for the analysis of total boron present in several lubrication oil additives and in several formulated lubrication oils. Values obtained by this method compare favorably with those obtained by other atomic emission spectroscopic (AES) methods. A direct current plasma (DCP) system has been optimized for the selective detection of boron in flowing organic liquid streams. A method was developed for the analysis of total boron present in several lubrication oil additives by flow injection analysis (FIA). A method was also developed for the qualitative separation [open quotes]speciation[close quotes] of these additives by size exclusion chromatography-DCP. Values obtained through this method compare favorably with values obtained through other AES methods. The MIP system was optimized for the selective detection of titanium in the effluent of the gas chromatograph. This system was used to analyze a group of reaction mixtures containing novel titanium chelates and organo-metallic compounds, as well as several organo-titanium-boron compounds. The MIP system was optimized for the selective detection of several of the group VA and group VIA elements in the effluent of the gas chromatograph. This system was used to characterize a series of coal standards (the Argonne Premium Coal Standards) by pyrolysis-GC-AES. Volatile compounds containing nitrogen, oxygen and sulfur were detected. The Py-GC-AES method was used to characterize several other coal, sedimentary and kerogen samples. Volatile phosphorous, arsenic, and selenium compounds were detected, as were compounds of nitrogen, oxygen and sulfur.

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

    PubMed

    Perring, Loïc; Basic-Dvorzak, Marija

    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. PMID:12324843

  10. Performance evaluation of four directional emissivity analytical models with thermal SAIL model and airborne images.

    PubMed

    Ren, Huazhong; Liu, Rongyuan; Yan, Guangjian; Li, Zhao-Liang; Qin, Qiming; Liu, Qiang; Nerry, Françoise

    2015-04-01

    Land surface emissivity is a crucial parameter in the surface status monitoring. This study aims at the evaluation of four directional emissivity models, including two bi-directional reflectance distribution function (BRDF) models and two gap-frequency-based models. Results showed that the kernel-driven BRDF model could well represent directional emissivity with an error less than 0.002, and was consequently used to retrieve emissivity with an accuracy of about 0.012 from an airborne multi-angular thermal infrared data set. Furthermore, we updated the cavity effect factor relating to multiple scattering inside canopy, which improved the performance of the gap-frequency-based models.

  11. Development of an analytical method for antimony speciation in vegetables by HPLC-hydride generation-atomic fluorescence spectrometry.

    PubMed

    Olivares, David; Bravo, Manuel; Feldmann, Jorg; Raab, Andrea; Neaman, Alexander; Quiroz, Waldo

    2012-01-01

    A new method for antimony speciation in terrestrial edible vegetables (spinach, onions, and carrots) was developed using HPLC with hydride generation-atomic fluorescence spectrometry. Mechanical agitation and ultrasound were tested as extraction techniques. Different extraction reagents were evaluated and optimal conditions were determined using experimental design methodology, where EDTA (10 mmol/L, pH 2.5) was selected because this chelate solution produced the highest extraction yield and exhibited the best compatibility with the mobile phase. The results demonstrated that EDTA prevents oxidation of Sb(III) to Sb(V) and maintains the stability of antimony species during the entire analytical process. The LOD and precision (RSD values obtained) for Sb(V), Sb(III), and trimethyl Sb(V) were 0.08, 0.07, and 0.9 microg/L and 5.0, 5.2, and 4.7%, respectively, for a 100 microL sample volume. The application of this method to real samples allowed extraction of 50% of total antimony content from spinach, while antimony extracted from carrots and onion samples ranged between 50 and 60 and 54 and 70%, respectively. Only Sb(V) was detected in three roots (onion and spinach) that represented 60-70% of the total antimony in the extracts.

  12. Four-level atom dynamics and emission statistics using a quantum jump approach

    NASA Astrophysics Data System (ADS)

    Sandhya, S. N.

    2007-01-01

    Four-level atom dynamics is studied in a ladder system in the nine parameter space consisting of driving field strengths, detunings and decay constants, {Ω1,Ω2,Ω3,Δ1,Δ2,Δ3,Γ2,Γ3,Γ4} . One can selectively excite or induce two-level behavior between particular levels of ones choice by appropriately tuning the driving field strengths at three-photon resonance. The dynamics may be classified into two main regions of interest (i) small Ω2 coupling the ∣2⟩-∣3⟩ transition and (ii) large Ω2 . In case (i) one sees two-level behavior consisting of adjacent levels and in a particular region in the parameter space, there is an intermittent shelving of the electrons in one of the two subsystems. In case (ii) the levels consist of the ground state and the upper most level. Emission statistics is studied using the delay function approach in both the cases. In case (i), the behavior of the second order correlation function g2(t) , is similar to that of two-level emission for low Ω1 coupling the ∣1⟩-∣2⟩ transition, and the correlation increases with Ω1 for smaller time delays. While, in case (ii) when, in addition, Ω3 coupling the ∣3⟩-∣4⟩ transitionis kept low, g2(t) shows superpoissonian distribution, which may be attributed to three-photon processes.

  13. 14 CFR 34.82 - Sampling and analytical procedures for measuring smoke exhaust emissions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. This document can be... measuring smoke exhaust emissions. 34.82 Section 34.82 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION... POWERED AIRPLANES Test Procedures for Engine Smoke Emissions (Aircraft Gas Turbine Engines) §...

  14. 14 CFR 34.82 - Sampling and analytical procedures for measuring smoke exhaust emissions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... Director of the Federal Register in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. This document can be... measuring smoke exhaust emissions. 34.82 Section 34.82 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION... POWERED AIRPLANES Test Procedures for Engine Smoke Emissions (Aircraft Gas Turbine Engines) §...

  15. 40 CFR 87.64 - Sampling and analytical procedures for measuring gaseous exhaust emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 1, 2011, report CO2 values along with your emission levels of regulated NOX to the Administrator for... on or after January 1, 2011. By January 1, 2011, report CO2 values along with your emission levels of... date of manufacture of the individual engine was before January 1, 2011. Round CO2 to the nearest 1...

  16. Fluorescence emission of Ca-atom from photodissociated Ca2 in Ar doped helium droplets. II. Theoretical.

    PubMed

    Hernando, A; Masson, A; Briant, M; Mestdagh, J-M; Gaveau, M-A; Halberstadt, N

    2012-11-14

    The stability of the ground or excited state calcium atom in an argon-doped helium droplet has been investigated using an extension of the helium density functional method to treat clusters. This work was motivated by the experimental study presented in a companion paper, hereafter called Paper I [A. Masson, M. Briant, J. M. Mestdagh, M. A. Gaveau, A. Hernando, and N. Halberstadt, J. Chem. Phys. 137, 184310 (2012)], which investigated Ca(2) photodissociation in an argon-doped helium droplet and the nature of the fluorescent species. It is found that one single argon atom is sufficient to bring the calcium atom inside the droplet, for droplets of over 200 helium atoms. The absorption and emission spectra of CaAr(M) (M = 0-7) clusters have been simulated using the recently developed density sampling method to describe the influence of the helium environment. Absorption spectra exhibit broad, double bands that are significantly blueshifted with respect to the calcium atomic line. The emission spectra are less broad and redshifted with respect to the calcium resonance line. The shifts are found to be additive only for M ≤ 2, because only the first two argon atoms are located in equivalent positions around the calcium p orbital. This finding gives a justification for the fit presented in the companion paper, which uses the observed shifts in the emission spectra as a function of argon pressure to deduce the shifts as a function of the number of argon atoms present in the cluster. An analysis of this fit is presented here, based on the calculated shifts. It is concluded that the emitting species following Ca(2) photodissociation in an argon-doped droplet in Paper I could be Ca∗Ar(M) in a partly evaporated droplet where less than 200 helium atoms remain.

  17. Spectral interferences in the determination of trace elements in environmental materials by inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Daskalova, N.; Boevski, I. V.

    1999-07-01

    This paper deals with spectral interferences in inductively coupled plasma atomic emission spectrometry (ICP-AES) encountered with environmental materials. These samples normally contain high concentrations of aluminium, calcium, magnesium, iron, titanium, potassium and sodium. The investigations cover: (a) spectral data for Al, Ca, Mg, Fe, Ti, K and Na as interferents for 200 pm wide windows centred (±100 pm) around the prominent lines of As, B, Ba, Be, Cd, Cr, Cu, Hg, Mn, P, Pb, Sb, Se, Sn, Tl, U and Zn; (b) a data base of Q-values for line interference [ QI j(λ a)] and Q-values for wing background interference [ QW j(Δλ a)] for two values of the excitation temperature 6200 K and 7200 K. The lines free or negligibly influenced by line interference were selected for analyte determination. Q-values were used for calculation of correction factors under a spectral line without the measurement of a reference blank at the wavelength of the prominent analysis lines. The accuracy of ICP-AES with the Q-concept as a basic methodology is checked by the analysis of a certified reference material IAEA/Sediment SD-N-1/2/. The precision of the method is characterised by an RSD of 0.6-1.7%. Extraction of trace elements soluble in aqua regia was used as a decomposition method. This article is an electronic publication in Spectrochimica Acta Electronica (SAE), a section of Spectrochimica Acta, Part B (SAB). The hardcopy text is accompanied by an electronic archive, stored on the SAE homepage at http://www.elsevier.nl/locate/sabe. The archive contains the tabular material of this article in electronic form.

  18. Method development for the determination of calcium, copper, magnesium, manganese, iron, potassium, phosphorus and zinc in different types of breads by microwave induced plasma-atomic emission spectrometry.

    PubMed

    Ozbek, Nil; Akman, Suleyman

    2016-06-01

    A novel method was developed for the determination of calcium, magnesium, potassium, iron, copper, zinc, and manganese and phosphorous in various kinds of breads samples sold in Turkey by microwave plasma-atomic emission spectrometry (MIP-AES). Breads were dried at 100 °C for one day, ground thoroughly and then digested using nitric acid/hydrogen per oxide (3:1). The analytes in certified reference wheat flour and maize flour samples were determined in the uncertainty limits of the certified values as well as the analytes added to the mixture of ground bread and acid mixture prior to digestion were recovered quantitatively (>90%). Therefore, all determinations were made by linear calibration technique using aqueous standards. The LOD values for Ca, Cu, Fe, K, Mg, Mn, P and Zn were 13.1, 0.28, 4.47, 118, 1.10, 0.41, 7550 and 3.00 ng mL(-1), respectively. No spectral interference was detected at the working wavelengths of the analytes. PMID:26830585

  19. Method development for the determination of calcium, copper, magnesium, manganese, iron, potassium, phosphorus and zinc in different types of breads by microwave induced plasma-atomic emission spectrometry.

    PubMed

    Ozbek, Nil; Akman, Suleyman

    2016-06-01

    A novel method was developed for the determination of calcium, magnesium, potassium, iron, copper, zinc, and manganese and phosphorous in various kinds of breads samples sold in Turkey by microwave plasma-atomic emission spectrometry (MIP-AES). Breads were dried at 100 °C for one day, ground thoroughly and then digested using nitric acid/hydrogen per oxide (3:1). The analytes in certified reference wheat flour and maize flour samples were determined in the uncertainty limits of the certified values as well as the analytes added to the mixture of ground bread and acid mixture prior to digestion were recovered quantitatively (>90%). Therefore, all determinations were made by linear calibration technique using aqueous standards. The LOD values for Ca, Cu, Fe, K, Mg, Mn, P and Zn were 13.1, 0.28, 4.47, 118, 1.10, 0.41, 7550 and 3.00 ng mL(-1), respectively. No spectral interference was detected at the working wavelengths of the analytes.

  20. CAPILLARY GAS CHROMATOGRAPHY-ATOMIC EMISSION DETECTION METHOD FOR THE DETERMINATION OF PENTYLATED ORGANOTIN COMPOUNDS: INTERLABORATORY STUDY

    EPA Science Inventory

    A capillary gas chromatography-atomic emission detection (GC-AED) method was developed for the U. S. Environmental Protection Agency's Environmental Monitoring Systems Laboratory in Las Vegas, NV, for determination of selected organotin compounds. Here we report on an interlabora...

  1. Identifying Student and Teacher Difficulties in Interpreting Atomic Spectra Using a Quantum Model of Emission and Absorption of Radiation

    ERIC Educational Resources Information Center

    Savall-Alemany, Francisco; Domènech-Blanco, Josep Lluís; Guisasola, Jenaro; Martínez-Torregrosa, Joaquín

    2016-01-01

    Our study sets out to identify the difficulties that high school students, teachers, and university students encounter when trying to explain atomic spectra. To do so, we identify the key concepts that any quantum model for the emission and absorption of electromagnetic radiation must include to account for the gas spectra and we then design two…

  2. Analytical estimation of emission zone mean position and width in organic light-emitting diodes from emission pattern image-source interference fringes

    SciTech Connect

    Epstein, Ariel Tessler, Nir Einziger, Pinchas D.; Roberts, Matthew

    2014-06-14

    We present an analytical method for evaluating the first and second moments of the effective exciton spatial distribution in organic light-emitting diodes (OLED) from measured emission patterns. Specifically, the suggested algorithm estimates the emission zone mean position and width, respectively, from two distinct features of the pattern produced by interference between the emission sources and their images (induced by the reflective cathode): the angles in which interference extrema are observed, and the prominence of interference fringes. The relations between these parameters are derived rigorously for a general OLED structure, indicating that extrema angles are related to the mean position of the radiating excitons via Bragg's condition, and the spatial broadening is related to the attenuation of the image-source interference prominence due to an averaging effect. The method is applied successfully both on simulated emission patterns and on experimental data, exhibiting a very good agreement with the results obtained by numerical techniques. We investigate the method performance in detail, showing that it is capable of producing accurate estimations for a wide range of source-cathode separation distances, provided that the measured spectral interval is large enough; guidelines for achieving reliable evaluations are deduced from these results as well. As opposed to numerical fitting tools employed to perform similar tasks to date, our approximate method explicitly utilizes physical intuition and requires far less computational effort (no fitting is involved). Hence, applications that do not require highly resolved estimations, e.g., preliminary design and production-line verification, can benefit substantially from the analytical algorithm, when applicable. This introduces a novel set of efficient tools for OLED engineering, highly important in the view of the crucial role the exciton distribution plays in determining the device performance.

  3. Applied analytical combustion/emissions research at the NASA Lewis Research Center

    NASA Technical Reports Server (NTRS)

    Deur, J. M.; Kundu, K. P.; Nguyen, H. L.

    1992-01-01

    Emissions of pollutants from future commercial transports are a significant concern. As a result, the Lewis Research Center (LeRC) is investigating various low emission combustor technologies. As part of this effort, a combustor analysis code development program was pursued to guide the combustor design process, to identify concepts having the greatest promise, and to optimize them at the lowest cost in the minimum time.

  4. Applied Analytical Combustion/emissions Research at the NASA Lewis Research Center - a Progress Report

    NASA Technical Reports Server (NTRS)

    Deur, J. M.; Kundu, K. P.; Nguyen, H. L.

    1992-01-01

    Emissions of pollutants from future commercial transports are a significant concern. As a result, the Lewis Research Center (LeRC) is investigating various low emission combustor technologies. As part of this effort, a combustor analysis code development program was pursued to guide the combustor design process, to identify concepts having the greatest promise, and to optimize them at the lowest cost in the minimum time.

  5. Spontaneous emission of “polarized” V-type three-level atoms strongly coupled with an optical cavity

    NASA Astrophysics Data System (ADS)

    Xue, Yan-Li; Zhu, Shi-Deng; Li, Jia-Fang; Ding, Wei; Feng, Bao-Hua; Li, Zhi-Yuan

    2015-03-01

    Polarization, an intrinsic ingredient of photon, plays a critical role in its interaction with matter. A general polarization state can be an appropriate superposition of two basic polarization states, say, the vertical and horizontal linear polarized state. Here we study spontaneous emission of a V-type three-level atom (with two upper states close in energy level) strongly coupled with a single-mode damped optical cavity. By defining a general polarization state of atom as a specific superposition of the two upper quantum states, we can prepare atoms with linear polarization at arbitrary direction, left and right circular polarization, and left and right elliptical polarization, similar to photons. We find that the spontaneous emission of light from these “polarized” three-level atoms shows very different profiles of side and axis spectra. This means that the polarization state of three-level atoms can become an active ingredient to manipulate its interaction with light and control the quantum interference effect. Exploitation of the coherent superposition and interference of quantum states in “polarized” atoms would allow one to deeply explore new frontiers of light-matter interaction. Project supported by the National Basic Research Foundation of China (Grant No. 2011CB922002).

  6. A technique coupling the analyte electrodeposition followed by in-situ stripping with electrothermal atomic absorption spectrometry for analysis of samples with high NaCl contents

    NASA Astrophysics Data System (ADS)

    Čánský, Zdeněk; Rychlovský, Petr; Petrová, Zuzana; Matousek, J. P.

    2007-03-01

    A technique coupling the analyte electrodeposition followed by in-situ stripping with electrothermal atomic absorption spectrometry has been developed for determination of lead and cadmium in samples with high salt contents. To separate the analyte from the sample matrix, the analyte was in-situ quantitatively electrodeposited on a platinum sampling capillary serving as the cathode (sample volume, 20 μL). The spent electrolyte containing the sample matrix was then withdrawn, the capillary with the analyte deposited was washed with deionized water and the analyte was stripped into a chemically simple electrolyte (5 g/L NH 4H 2PO 4) by reversing the polarity of the electrodeposition circuit. Electrothermal atomization using a suitable optimized temperature program followed. A fully automated manifold was designed for this coupled technique and the appropriate control software was developed. The operating conditions for determination of Pb and Cd in samples with high contents of inorganic salts were optimized, the determination was characterized by principal analytical parameters and its applicability was verified on analyses of urine reference samples. The absolute limits of detection for lead and cadmium (3 σ criterion) in a sample containing 30 g/L NaCl were 8.5 pg and 2.3 pg, respectively (peak absorbance) and the RSD values amounted to 1.6% and 1.9% for lead (at the 40 ng mL - 1 level) and cadmium (at the 4.0 ng mL - 1 level), respectively. These values (and also the measuring sensitivity) are superior to the results attained in conventional electrothermal atomic absorption spectrometric determination of Pb and Cd in pure solutions (5 g/L NH 4H 2PO 4). The sensitivity of the Pb and Cd determination is not affected by the NaCl concentration up to a value of 100 g/L, demonstrating an efficient matrix removal during the electrodeposition step.

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

    SciTech Connect

    Nilsson, A.; Wassdahl, N.; Weinelt, M.

    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.

  8. Practicality of Using Oxygen Atom Emissions to Evaluate the Habitability of Extra-Solar Planets

    NASA Astrophysics Data System (ADS)

    Slanger, T. G.

    2005-12-01

    It has previously been proposed [Akasofu, 1999] that observation of the O(1S - 1D) green line from the atmospheres of extra-solar planets might be a marker for habitability. Guidance on this question is available within our own solar system. The green line is a dominant feature in the visible terrestrial nightglow, and the ultimate origin of its mesospheric emission is the three-body recombination of oxygen atoms. Until recently, it was believed that the green line was not a feature of the nightglows of the CO2 planets, Venus and Mars. It is now known that Venus at times shows green line emission with an intensity equal to terrestrial values [Slanger et al., 2001]. Furthermore, the intensity is quite variable, as is true for the much stronger O2( a-X) 1.27 μ emission. Recent observations of the Mars nightglow [Bertaux et al., 2005] give ambiguous results in the region of the O(1S-3P) line at 297.2 nm, but the same line in the dayglow is very strong, as evidenced in earlier Mariner results [Barth et al., 1971], and from the recent Mars Express data [F. Leblanc, private communication]. The O(1D-3P) 630 nm red line is a feature associated with Io, where dissociation of SO2 is a presumed source [Scherb et al., 1998]. Thus, observation of the oxygen green/red lines in the atmospheres of extrasolar planets provides insufficient information to reach conclusions about a habitable environment. Such detection would only indicate that there are oxygen-containing molecules present. Determination of an O2 column depth, by Fraunhofer A-band absorption, would be much more conclusive. Akasofu, S.-I., EOS, Transactions of the American Geophysical Union, 80, 397, 1999. Barth, C.A., C.W. Hord, J.B. Pearce, K.K. Kelly, G.P. Anderson, and A.I. Stewart, Mariner 6 and 7 Ultraviolet Spectrometer Experiment: Upper Atmosphere Data, Journal of Geophysical Research, 76, 2213-2227, 1971. Bertaux, J.-L., F. Leblanc, S. Perrier, E. Quemerais, O. Korablev, E. Dimarellis, A. Reberac, F. Forget, P

  9. Analytical combustion/emissions research related to the NASA high-speed research program

    NASA Technical Reports Server (NTRS)

    Nguyen, H. Lee

    1991-01-01

    Increasing the pressure and temperature of the engines of new generation supersonic airliners increases the emissions of nitrogen oxides to a level that would have an adverse impact on the Earth's protective ozone layer. In the process of implementing low emissions combustor technologies, NASA Lewis Research Center has pursued a combustion analysis program to guide combustor design processes, to identify potential concepts of greatest promise, and to optimize them at low cost, with short turn-around time. The approach is to upgrade and apply advanced computer programs for gas turbine applications. Efforts have been made to improve the code capabilities of modeling the physics. Test cases and experiments are used for code validation. To provide insight into the combustion process and combustor design, two-dimensional and three-dimensional codes such as KIVA-II and LeRC 3D have been used. These codes are operational and calculations have been performed to guide low emissions combustion experiments.

  10. [Atomic emission spectrometry determination of Au, Pt and Pd after separation and enrichment by hyperbranched polymer].

    PubMed

    Li, Hui-Zhi; Zhai, Dian-Tang; Shou, Chong-Qi; Zhao, Shu-Ying; Wei, Qin

    2006-09-01

    The present paper shows that the trace amount of gold, platinum and palladium in hydrochloric acid solution can be concentrated by hyperbranched polymer. The new reagent has a rapid adsorption rate and big concentrating capacity. The determination of trace Au, Pt and Pd in sample using carbon powder and strontium carbonate as buffer was carried out by atomic emission spectrometry(AES). Zirconium was selected as internal standard line. The sample was directly loaded into ordinary electrode. The method is simple, rapid and accurate. The condition of determination, and factors of influence were studied. The analysis line of Au, Pt and Pd is 312.3, 306.5 and 311.4 nm respectively. The internal standard line of Zr is 310.7 nm. The linear range of the determination of Au, Pt and Pd is 0-0. 20%, 0-0. 40% and 0-0. 20% respectively. The detection limit of Au, Pt and Pd is 0.010%, 0.0030% and 0.0030% respectively. The method has been applied to the determination of Au, Pt and Pd with satisfactory results.

  11. 40 CFR 86.107-96 - Sampling and analytical systems; evaporative emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... sealed, the enclosure shall be gas tight in accordance with § 86.117-96. Interior surfaces must be... emission testing: (i) Variable-volume enclosure. The variable-volume enclosure expands and contracts in...) inside the enclosure expand and contract in response to internal pressure changes by exchanging air...

  12. 40 CFR 86.107-96 - Sampling and analytical systems; evaporative emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... sealed, the enclosure shall be gas tight in accordance with § 86.117-96. Interior surfaces must be... emission testing: (i) Variable-volume enclosure. The variable-volume enclosure expands and contracts in...) inside the enclosure expand and contract in response to internal pressure changes by exchanging air...

  13. 40 CFR 86.107-96 - Sampling and analytical systems; evaporative emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... air circulation blower(s) shall be configured to provide a well dispersed air circulation pattern that... temperature during all evaporative emission test segments, as well as vehicle fuel tank temperature during the... an enclosure, as well as the vehicle's fuel tank pressure during the running loss test and...

  14. 40 CFR 86.107-96 - Sampling and analytical systems; evaporative emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... air circulation blower(s) shall be configured to provide a well dispersed air circulation pattern that... temperature during all evaporative emission test segments, as well as vehicle fuel tank temperature during the... an enclosure, as well as the vehicle's fuel tank pressure during the running loss test and...

  15. 40 CFR 87.64 - Sampling and analytical procedures for measuring gaseous exhaust emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... ICAO Annex 16 (incorporated by reference in § 87.8). (b) Starting January 1, 2011, report CO2 values.... By January 1, 2011, report CO2 values along with your emission levels of regulated NOX to the... the individual engine was before January 1, 2011. Round CO2 to the nearest 1 g/kilonewton rO....

  16. 40 CFR 87.64 - Sampling and analytical procedures for measuring gaseous exhaust emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...) (b) Starting January 1, 2011, report CO2 values along with your emission levels of regulated NOX to... individual production model was on or after January 1, 2011. By January 1, 2011, report CO2 values along with.... Round CO2 to the nearest 1 g/kilonewton rO. (c) Report CO2 by calculation from fuel mass flow...

  17. Direct observation of electron emission from the grain boundaries of chemical vapour deposition diamond films by tunneling atomic force microscopy

    SciTech Connect

    Chatterjee, Vijay; Harniman, Robert; May, Paul W.; Barhai, P. K.

    2014-04-28

    The emission of electrons from diamond in vacuum occurs readily as a result of the negative electron affinity of the hydrogenated surface due to features with nanoscale dimensions, which can concentrate electric fields high enough to induce electron emission from them. Electrons can be emitted as a result of an applied electric field (field emission) with possible uses in displays or cold-cathode devices. Alternatively, electrons can be emitted simply by heating the diamond in vacuum to temperatures as low as 350 °C (thermionic emission), and this may find applications in solar energy generation or energy harvesting devices. Electron emission studies usually use doped polycrystalline diamond films deposited onto Si or metallic substrates by chemical vapor deposition, and these films have a rough, faceted morphology on the micron or nanometer scale. Electron emission is often improved by patterning the diamond surface into sharp points or needles, the idea being that the field lines concentrate at the points lowering the barrier for electron emission. However, there is little direct evidence that electrons are emitted from these sharp tips. The few reports in the literature that have studied the emission sites suggested that emission came from the grain boundaries and not the protruding regions. We now present direct observation of the emission sites over a large area of polycrystalline diamond using tunneling atomic force microscopy. We confirm that the emission current comes mostly from the grain boundaries, which is consistent with a model for emission in which the non-diamond phase is the source of electrons with a threshold that is determined by the surrounding hydrogenated diamond surface.

  18. Experimental and analytical investigation of the variation of spray characteristics along a radial distance downstream of a pressure-swirl atomizer

    NASA Technical Reports Server (NTRS)

    Chin, J. S.; Li, W. M.; Wang, X. F.

    1986-01-01

    The variation of spray characteristics along a radial distance downstream of a pressure-swirl atomizer was measured by laser light-scattering technology. An analytical model was developed to predict the variation of spray characteristics along the radial distance. A comparison of the predicted and experimental data showed excellent agreement. Therefore, the spray model proposed, although relatively simple, is correct and can be used, with some expansion and modification of the prepared model, to predict more complicated spray systems.

  19. Synchrotron and inverse-Compton emissions from pairs formed in GRB afterglows (analytical treatment)

    SciTech Connect

    Panaitescu, A.; Vestrand, W. T.

    2014-10-01

    We calculate the synchrotron and inverse-Compton emissions from pairs formed in gamma-ray burst (GRB) afterglows from high-energy photons (above 100 MeV), assuming a power-law photon spectrum C {sub ν}∝ν{sup –2} and considering only the pairs generated from primary high-energy photons. The essential properties of these pairs (number, minimal energy, cooling energy, distribution with energy) and of their emission (peak flux, spectral breaks, spectral slope) are set by the observables GeV fluence Φ(t) = Ft and spectrum, and by the Lorentz factor, Γ, and magnetic field, B, of the source of high-energy photons, at observer time, t. Optical and X-ray pseudo light curves, F {sub ν}(Γ), are calculated for the given B; proper synchrotron self-Compton light curves are calculated by setting the dynamics Γ(t) of the high-energy photon source to be that of a decelerating, relativistic shock. It is found that the emission from pairs can accommodate the flux and decays of the optical flashes measured during the prompt (GRB) phase, but it decays faster than the X-ray plateaus observed during the delayed (afterglow) phase. The brightest pair optical emission is obtained for 100 < Γ < 500, and depends mostly on the GeV fluence, being independent of the source redshift. Emission from pairs formed during the GRB phase offers an alternate explanation to reverse-shock optical flashes. These two models may be distinguished based on their corresponding flux decay index-spectral slope relations, different correlations with the Large Area Telescope fluence, or through modeling of the afterglow multiwavelength data.

  20. Energetic ion, atom, and molecule reactions and excitation in low-current H2 discharges: spatial distributions of emissions.

    PubMed

    Petrović, Z Lj; Phelps, A V

    2009-07-01

    Spatial distributions of H alpha , H beta , and the near-uv continuum emission from the H2 a ;{3}Sigma g;+ state are measured and compared with a model for low-current electrical discharges in H2 at high E/N and low Nd , where E is the spatially uniform electric field, N is the gas density, and d is the electrode separation. Data are analyzed for 300 Tdatoms and molecules with mean energies from 5 to 1500 eV. Electron-induced emission, dominant at low E/N and low pressures, is distinguished by its buildup toward the anode. Excitation of H alpha by fast H atoms dominates at high E/N and increases toward the cathode. The observed H alpha emission at low E/N is normalized to previous experiments to yield absolute experimental excitation coefficients for all E/N and Nd . Small adjustments of model parameters yield good agreement with H alpha data. Cross sections are derived for excitation of the H2 near-uv continuum by H atoms. Spatial and pressure dependencies of H alpha and H2 near-uv emissions agree well with a model in which reactions of H2+ , H3+ , and H+ ions with H2 lead to fast H atoms and H2 molecules, which then excite H atoms or H2 molecules. PMID:19658824

  1. Emergence of non-Markovianity in the emission process of an atom in a half-cavity

    NASA Astrophysics Data System (ADS)

    Tufarelli, Tommaso; Kim, M. S.; Ciccarello, Francesco

    2014-04-01

    We study quantum non-Markovianity in the early stage of the emission process of a two-level atom coupled to a semi-infinite waveguide, where the waveguide termination behaves like a perfect mirror. Specifically, we restrict ourselves to analysis of the process for times shorter than twice the time delay td, where td is the duration of a round trip along the atom-mirror path. We show the emergence of a threshold in the parameter space separating the Markovian and non-Markovian regions.

  2. Analytic treatment of source photon emission times to reduce noise in implicit Monte Carlo calculations

    SciTech Connect

    Trahan, Travis J.; Gentile, Nicholas A.

    2012-09-10

    Statistical uncertainty is inherent to any Monte Carlo simulation of radiation transport problems. In space-angle-frequency independent radiative transfer calculations, the uncertainty in the solution is entirely due to random sampling of source photon emission times. We have developed a modification to the Implicit Monte Carlo algorithm that eliminates noise due to sampling of the emission time of source photons. In problems that are independent of space, angle, and energy, the new algorithm generates a smooth solution, while a standard implicit Monte Carlo solution is noisy. For space- and angle-dependent problems, the new algorithm exhibits reduced noise relative to standard implicit Monte Carlo in some cases, and comparable noise in all other cases. In conclusion, the improvements are limited to short time scales; over long time scales, noise due to random sampling of spatial and angular variables tends to dominate the noise reduction from the new algorithm.

  3. Semi-analytical emission model for diffusion flame, rich/lean and premixed lean combustors

    NASA Astrophysics Data System (ADS)

    Rizk, N. K.; Mongia, H. C.

    1995-04-01

    To enhance gas turbine combustor performance and emissions characteristics, better design methods need to be developed. In the present investigation, an emission model that simulates a detailed chemical kinetic scheme has been developed to provide the rate of reactions of the parent fuel, an intermediate hydrocarbon compound, CO, and H2. The intermediate fuel has variable carbon and hydrogen contents depending on operating conditions, that were selected in the development effort to simulate actual operation of rich/lean, diffusion flame, and lean combustor concepts. The developed reaction rate expressions address also the limited reaction rates that may occur in the near-wall regions of the combustor due to the admittance of radial air jets and cooling air in these regions. The validation effort included the application of the developed model to a combustor simulated by a multiple-reactor arrangement. The results indicate the accurate duplication of the calculations obtained from the detailed kinetic scheme using the developed model. This illustrates the great potential of using such a unified approach to guide the design of various types of combustor to meet the more stringent emissions and performance requirements of next-generation gas turbine engines.

  4. An analytical study of nitrogen oxides and carbon monoxide emissions in hydrocarbon combustion with added nitrogen, preliminary results

    NASA Technical Reports Server (NTRS)

    Bittker, D. A.

    1979-01-01

    The effect of combustor operating conditions on the conversion of fuel-bound nitrogen (FBN) to nitrogen oxides NO sub x was analytically determined. The effect of FBN and of operating conditions on carbon monoxide (CO) formation was also studied. For these computations, the combustor was assumed to be a two stage, adiabatic, perfectly-stirred reactor. Propane-air was used as the combustible mixture and fuel-bound nitrogen was simulated by adding nitrogen atoms to the mixture. The oxidation of propane and formation of NO sub x and CO were modeled by a fifty-seven reaction chemical mechanism. The results for NO sub x and CO formation are given as functions of primary and secondary stage equivalence ratios and residence times.

  5. Analytical Applications Of Particle-Induced X-Ray Emission (PIXE)

    SciTech Connect

    Popescu, I. V.; Stihi, C.; Bancuta, A.; Dima, G.; Ene, A.; Badica, T.; Ghisa, V.

    2007-04-23

    In this paper a complex study of the capabilities of Particle-Induced X-ray Emission (PIXE) technique for the determination of major, minor and trace constituents of metallurgical, biological and environmental samples has been done. The elements identified in the metallurgical samples (steels) using PIXE were: K, Ca, V, Cr, Mn, Fe, Co, Cu, Ni, Zn, W, Ga, As, Pb, Mo, Rb, In, Rh, Zr, Pd, Nb, Sn and Sb. In the investigated biological and environmental samples (vegetals leaves, soil and mosses) PIXE analysis allowed determination of: S, Cl, K, Ca, Ti, Mn, Fe, Ni, Cu, Zn, As, Hg and Pb.

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

    NASA Astrophysics Data System (ADS)

    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.

  7. Identifying student and teacher difficulties in interpreting atomic spectra using a quantum model of emission and absorption of radiation

    NASA Astrophysics Data System (ADS)

    Savall-Alemany, Francisco; Domènech-Blanco, Josep Lluís; Guisasola, Jenaro; Martínez-Torregrosa, Joaquín

    2016-06-01

    Our study sets out to identify the difficulties that high school students, teachers, and university students encounter when trying to explain atomic spectra. To do so, we identify the key concepts that any quantum model for the emission and absorption of electromagnetic radiation must include to account for the gas spectra and we then design two questionnaires, one for teachers and the other for students. By analyzing the responses, we conclude that (i) teachers lack a quantum model for the emission and absorption of electromagnetic radiation capable of explaining the spectra, (ii) teachers and students share the same difficulties, and (iii) these difficulties concern the model of the atom, the model of radiation, and the model of the interaction between them.

  8. Gunshot residue testing in suicides: Part II: Analysis by inductive coupled plasma-atomic emission spectrometry.

    PubMed

    Molina, D Kimberley; Castorena, Joe L; Martinez, Michael; Garcia, James; DiMaio, Vincent J M

    2007-09-01

    Several different methods can be employed to test for gunshot residue (GSR) on a decedent's hands, including scanning electron microscopy with energy dispersive x-ray (SEM/EDX) and inductive coupled plasma-atomic emission spectrometry (ICP-AES). In part I of this 2-part series, GSR results performed by SEM/EDX in undisputed cases of suicidal handgun wounds were studied. In part II, the same population was studied, deceased persons with undisputed suicidal handgun wounds, but GSR testing was performed using ICP-AES. A total of 102 cases were studied and analyzed for caliber of weapon, proximity of wound, and the results of the GSR testing. This study found that 50% of cases where the deceased was known to have fired a handgun immediately prior to death had positive GSR results by ICP/AES, which did not differ from the results of GSR testing by SEM/EDX. Since only 50% of cases where the person is known to have fired a weapon were positive for GSR by either method, this test should not be relied upon to determine whether someone has discharged a firearm and is not useful as a determining factor of whether or not a wound is self-inflicted or non-self-inflicted. While a positive GSR result may be of use, a negative result is not helpful in the medical examiner setting as a negative result indicates that either a person fired a weapon prior to death or a person did not fire a weapon prior to death.

  9. Activation of extended red emission photoluminescence in carbon solids by exposure to atomic hydrogen and UV radiation

    NASA Technical Reports Server (NTRS)

    Furton, Douglas G.; Witt, Adolf N.

    1993-01-01

    We report on new laboratory results which relate directly to the observation of strongly enhanced extended red emission (ERE) by interstellar dust in H2 photodissociation zones. The ERE has been attributed to photoluminescence by hydrogenated amorphous carbon (HAC). We are demonstrating that exposure to thermally dissociated atomic hydrogen will restore the photoluminescence efficiency of previously annealed HAC. Also, pure amorphous carbon (AC), not previously photoluminescent, can be induced to photoluminesce by exposure to atomic hydrogen. This conversion of AC into HAC is greatly enhanced by the presence of UV irradiation. The presence of dense, warm atomic hydrogen and a strong UV radiation field are characteristic environmental properties of H2 dissociation zones. Our results lend strong support to the HAC photoluminescence explanation for ERE.

  10. Atomizing characteristics of swirl can combustor modules with swirl blast fuel injectors. [in terms of NOX emission rate

    NASA Technical Reports Server (NTRS)

    Ingebo, R. D.

    1980-01-01

    Cold flow atomization tests of several different designs of swirl can combustor modules were conducted in a 7.6 cm diameter duct at airflow rates (per unit area) of 7.3 to 25.7 g/sq cm sec and water flow rates of 6.3 to 18.9 g/sec. The effect of air and water flow rates on the mean drop size of water sprays produced with the swirl blast fuel injectors were determined. Also, from these data it was possible to determine the effect of design modifications on the atomizing performance of various fuel injector and air swirler configurations. The trend in atomizing performance, as based on the mean drop size, was then compared with the trends in the production of nitrogen oxides obtained in combustion studues with the same swirl can combustors. It was found that the fuel injector design that gave the best combustor performance in terms of a low NOx emission index also gave the best atomizing performance as characterized by a spray of relatively small mean drop diameter. It was also demonstrated that at constant inlet air stream momentum the nitrogen oxides emission index was found to vary inversely with the square of the mean drop diameter of the spray produced by the different swirl blast fuel injectors. Test conditions were inlet air static pressures of 100,000 to 200,000 N/sq m at an inlet air temperature of 293 K.

  11. Exploring star formation in high-z galaxies using atomic and molecular emission lines

    NASA Astrophysics Data System (ADS)

    Gullberg, Bitten

    2016-03-01

    The conditions under which stars are formed and the reasons for triggering and quenching of starburst events in high-z galaxies, are still not well understood. Studying the interstellar medium (ISM) and the morphology of high-z galaxies are therefore key points in order to understand galaxy evolution. The cosmic star formation rate density peaks between 1>1, and low to moderate [CII] optical depth tau(CII)<1. Combining millimetre/sub-millimetre and optical data cubes for the high-z radio galaxy (HzRG) MRC0943-242, has revealed a much more complicated morphology than seen in the individual data sets. The millimetre/sub-millimetre observations data have allowed us to spatially separate of the AGN and starburst dominated components, which ~65 kpc apart. The optical data reveal structures of emitting and absorbing gas at multiple wavelengths. A deep high resolution millimetre/sub-millimetre study of the HzRG MRC1138-262, shows emission from water (H2O) and an unusually large amount of neutral atomic carbon ([CI]) relative to highly excited CO compared to lensed DSFGs. The

  12. Sampling/analytical method evaluation for ethylene oxide emission and control-unit efficiency determinations

    SciTech Connect

    Steger, J.; Gergen, W.; Margeson, J.H.

    1988-05-01

    Radian Corporation, assisting the Environmental Monitoring Systems Laboratory, Environmental Protection Agency, Research Triangle Park, North Carolina, performed a field evaluation of a method for sampling and analyzing ethylene oxide (EO) in the vent stream from a sterilization chamber and a dilute-acid scrubber. The utility of the sampling method for measuring the efficiency of the control unit was also evaluated. The evaluated sampling and analysis procedure used semi-continuous direct sampling with on-line gas chromatographic analysis. Laboratory studies of the sampling method previous to the field test showed that semi-continuous direct sampling was capable of measuring EO emissions to within 11% of the expected value with a between-trial precision of 5%.

  13. Zeeman effects in the hyperfine structure of atomic iodine photodissociation laser emission.

    NASA Technical Reports Server (NTRS)

    Hwang, W. C.; Kasper, J. V. V.

    1972-01-01

    Observation of hyperfine structure in laser emission from CF3I and C2F5I photodissociation lasers. Constant magnetic fields affect the time behavior of the emission by changing the relative gains of the hyperfine transitions. Time-varying fields usually present in photodissociation lasers further complicate the emission.

  14. The atomic oxygen green and red line emission response to sudden impulses of the solar wind dynamic pressure.

    NASA Astrophysics Data System (ADS)

    Leonovich, Ludmila; Leonovich, Vitaly; Tashchilin, Anatoly

    The atomic oxygen green and red line emission response to sudden impulses of the solar wind dynamic pressure was revealed at mid-latitudes. The paper presents the study results of the dependence of the observed emissions intensity from the sudden variations in the solar wind and the geomagnetic field. These results show a relationship of the emissions disturbance amplitude with the solar wind speed, as well as with the geomagnetic field variations. We used the zenith photometer optical data, the geomagnetic field and the total electron content variations obtained for the Eastern Siberia region (52(°) N, 103(°) E). The investigation was supported by the RFFI grants № 12-05-00024-а, № 13-05-00733.

  15. An `analytic dynamical magnetosphere' formalism for X-ray and optical emission from slowly rotating magnetic massive stars

    NASA Astrophysics Data System (ADS)

    Owocki, Stanley P.; ud-Doula, Asif; Sundqvist, Jon O.; Petit, Veronique; Cohen, David H.; Townsend, Richard H. D.

    2016-11-01

    Slowly rotating magnetic massive stars develop `dynamical magnetospheres' (DMs), characterized by trapping of stellar wind outflow in closed magnetic loops, shock heating from collision of the upflow from opposite loop footpoints, and subsequent gravitational infall of radiatively cooled material. In 2D and 3D magnetohydrodynamic (MHD) simulations, the interplay among these three components is spatially complex and temporally variable, making it difficult to derive observational signatures and discern their overall scaling trends. Within a simplified, steady-state analysis based on overall conservation principles, we present here an `analytic dynamical magnetosphere' (ADM) model that provides explicit formulae for density, temperature, and flow speed in each of these three components - wind outflow, hot post-shock gas, and cooled inflow - as a function of colatitude and radius within the closed (presumed dipole) field lines of the magnetosphere. We compare these scalings with time-averaged results from MHD simulations, and provide initial examples of application of this ADM model for deriving two key observational diagnostics, namely hydrogen H α emission line profiles from the cooled infall, and X-ray emission from the hot post-shock gas. We conclude with a discussion of key issues and advantages in applying this ADM formalism towards derivation of a broader set of observational diagnostics and scaling trends for massive stars with such dynamical magnetospheres.

  16. Antimony in drinking water, red blood cells, and serum: development of analytical methodology using transversely heated graphite furnace atomization-atomic absorption spectrometry.

    PubMed

    Subramanian, K S; Poon, R; Chu, I; Connor, J W

    1997-05-01

    An atomic absorption spectrometric (AAS) method has been developed for determining microg/L levels of Sb in samples of water and blood. The AAS method is based on the concept of stabilized temperature platform furnace atomization (STPF) realized through the use of a transversely heated graphite atomizer (THGA) furnace, longitudinal Zeeman-effect background correction, and matrix modification with palladium nitrate-magnesium nitrate-nitric acid. The method of standard additions is not mandatory. The detection limit (3 standard deviations of the blank) is 2.6 microg Sb/L for the water, red blood cells (RBCs), and serum samples. Data are presented on the degree of accuracy and precision. The THGA-AAS method is simple, fast, and contamination-free because the entire operation from sampling to AAS measurement is carried out in the same tube. The method has been applied to the determination of Sb in some leachate tap water samples derived from a static copper plumbing system containing Sn/Sb solders, and in small samples (0.5 ml) of RBCs and serum derived from rats given Sb-supplemented drinking water. PMID:9175512

  17. Inductively coupled plasma -- Atomic emission spectroscopy glove box assembly system at the West Valley Demonstration Project

    SciTech Connect

    Marlow, J.H.; McCarthy, K.M.; Tamul, N.R.

    1999-12-17

    The inductively coupled plasma/atomic emission spectroscopy [ICP/AES (ICP)] system for elemental analyses in support of vitrification processing was first installed in 1986. The initial instrument was a Jobin Yvon (JY) Model JY-70 ICP that consisted of sequential and simultaneous spectrometers for analysis of nonradioactive samples as radioactive surrogates. The JY-70 ICP continued supporting nonradioactive testing during the Functional and Checkout Testing of Systems (FACTS) using the full-scale melter with ``cold'' (nonradioactive) testing campaigns. As a result, the need for another system was identified to allow for the analysis of radioactive samples. The Mass Spec (Spectrometry) Lab was established for the installation of the modified ICP system for handling radioactive samples. The conceptual setup of another ICP was predicated on the use of a hood to allow ease of accessibility of the torch, nebulizer, and spray chamber, and the minimization of air flow paths. However, reconsideration of the radioactive sample dose rate and contamination levels led to the configuration of the glovebox system with a common transfer interface box for the ICP and the inductively coupled plasma-mass spectrometer (ICP-MS) glovebox assemblies. As a result, a simultaneous Model JY-50P ICP with glovebox was installed in 1990 as a first generation ICP glovebox system. This was one of the first ICP glovebox assemblies connected with an ICP-MS glovebox system. Since the economics of processing high-level radioactive waste (HLW) required the availability of an instrument to operate 24 hours a day throughout the year without any downtime, a second generation ICP glovebox assembly was designed, manufactured, and installed in 1995 using a Model JY-46P ICP. These two ICP glovebox systems continue to support vitrification of the HLW into canisters for storage. The ICP systems have been instrumental in monitoring vitrification batch processing. To date, remote sample preparation and

  18. Bias and uncertainty in the absorption emission measurement of atomic sodium density in the SSME exit plane

    NASA Technical Reports Server (NTRS)

    Bauman, Leslie E.

    1990-01-01

    The measurement of atomic sodium concentration in the TTB 019 firing of April 1990 is significant in that it represents the first measurement of density at the exit plane of the space shuttle main engine. The knowledge of the sodium density, combined with the certainty that the exit plane of the plume is optically thin at the sodium D-line wavelengths, provides essential information for evaluation of diagnostic techniques using sodium atoms, such as resonant Doppler velocimetry for temperature, pressure, and velocity through high resolution fluorescent lineshape analysis. The technique used for the sodium atom line transmission (SALT) measurements is that of resonant absorption emission using a hollow cathode lamp as the reference source. Through the use of two-dimensional kinetic (TDK) predictions of temperature and density for the flight engine case and radiative transfer calculations, this line-of-sight spectrally integrated transmission indicates a sodium atom concentration, i.e., mole fraction, of 0.91e-10. The subject of this paper is the assumptions and measurement uncertainties tied into the calculation. Because of the narrow shape of the source emission, the uncertainties in the absorption profile could introduce considerable bias in the measurement. The following were investigated: (1) the inclusion of hyperfine splitting of the D-lines in the calculation; (2) the use of the flight engine predictions of plume temperature and density versus those for the large throat engine; (3) the assumption of a Gaussian, i.e., Doppler, distribution for the source radiance with a temperature of 400 K; (4) the use of atomic collisional shift and width values for the work by Jongerius; and (5) a Doppler shift for a 7 degree outward velocity vector at the plume edge. Also included in the study was the bias introduced by an uncertainty in the measurement of the D1/D2 line ratio in the source.

  19. Cross sections for ionization of K, L and M shells of atoms by impact of electrons and positrons with energies up to 1 GeV: Analytical formulas

    SciTech Connect

    Bote, David; Salvat, Francesc Jablonski, Aleksander

    2009-11-15

    Analytical formulas are presented for the easy calculation of cross sections for ionization of K, L and M shells of neutral atoms by impact of electrons and positrons with kinetic energies up to 1 GeV. Each formula contains a number of parameters that are characteristic of the element, the active electron shell and the projectile particle. The values of these parameters were determined by fitting the cross section values in an extensive database that was calculated recently by means of a composite algorithm that combines the distorted-wave and plane-wave Born approximations. Tables of parameter values are given for all elements, from hydrogen (Z=1) to einsteinium (Z=99). The proposed analytical expressions yield ionization cross sections that agree with those in the numerical database to within about 1%, except for projectiles with near-threshold energies.

  20. Cross sections for ionization of K, L and M shells of atoms by impact of electrons and positrons with energies up to 1 GeV: Analytical formulas

    NASA Astrophysics Data System (ADS)

    Bote, David; Salvat, Francesc; Jablonski, Aleksander; Powell, Cedric J.

    2009-11-01

    Analytical formulas are presented for the easy calculation of cross sections for ionization of K, L and M shells of neutral atoms by impact of electrons and positrons with kinetic energies up to 1 GeV. Each formula contains a number of parameters that are characteristic of the element, the active electron shell and the projectile particle. The values of these parameters were determined by fitting the cross section values in an extensive database that was calculated recently by means of a composite algorithm that combines the distorted-wave and plane-wave Born approximations. Tables of parameter values are given for all elements, from hydrogen (Z=1) to einsteinium (Z=99). The proposed analytical expressions yield ionization cross sections that agree with those in the numerical database to within about 1%, except for projectiles with near-threshold energies.

  1. Use of multiwavelength emission from hollow cathode lamp for measurement of state resolved atom density of metal vapor produced by electron beam evaporation

    SciTech Connect

    Majumder, A.; Dikshit, B.; Bhatia, M. S.; Mago, V. K.

    2008-09-15

    State resolved atom population of metal vapor having low-lying metastable states departs from equilibrium value. It needs to be experimentally investigated. This paper reports the use of hollow cathode lamp based atomic absorption spectroscopy technique to measure online the state resolved atom density (ground and metastable) of metal vapor in an atomic beam produced by a high power electron gun. In particular, the advantage of availability of multiwavelength emission in hollow cathode lamp is used to determine the atom density in different states. Here, several transitions pertaining to a given state have also been invoked to obtain the mean value of atom density thereby providing an opportunity for in situ averaging. It is observed that at higher source temperatures the atoms from metastable state relax to the ground state. This is ascribed to competing processes of atom-atom and electron-atom collisions. The formation of collision induced virtual source is inferred from measurement of atom density distribution profile along the width of the atomic beam. The total line-of-sight average atom density measured by absorption technique using hollow cathode lamp is compared to that measured by atomic vapor deposition method. The presence of collisions is further supported by determination of beaming exponent by numerically fitting the data.

  2. Atomic Processes in Emission Characteristics of a Lithium Plasma Plume Formed by Double-Pulse Laser Ablation

    NASA Astrophysics Data System (ADS)

    Sivakumaran, V.; Ajai, Kumar; K. Singh, R.; Prahlad, V.; C. Joshi, H.

    2013-03-01

    High resolution spectral analysis of lithium plasma formed by single and double laser ablation has been undertaken to understand the plume-laser interaction, especially at the early stages of the plasma plume. In order to identify different atomic processes in evolving plasma, time resolved spectral emission studies at different inter-pulse delays have been performed for ionic and neutral lithium lines emitting from different levels. Along with the enhancement in emission intensity, a large line broadening and spectral shift, especially in the case of excited state transition Li I 610.3 nm have been observed in the presence of the second pulse. This broadening and shift gradually decrease with increasing time delay. Another interesting feature is the appearance of a multi-component structure in the ionic line at 548.4 nm and these components change conversely into a single structure at the later stages of the plasma. The multi-component structures are correlated with the presence of different velocity (temperature) distributions in non-LTE conditions. Atomic analyses by computing photon emissivity coefficients with an ADAS code have been used to identify the above processes.

  3. AGB circumstellar environments probed through the 21 cm atomic hydrogen line emission. A programme for the SKA?

    NASA Astrophysics Data System (ADS)

    Gerard, E.; Le Bertre, T.

    2006-06-01

    Red giant stars are responsible for 70% of the recycling of stellar matter in the local interstellar medium (ISM) through mass loss, mainly along the AGB sequence. Most of the matter in circumstellar shells is hydrogen in atomic (or molecular form). However, up to now, atomic hydrogen has remained largely undetected due to the weakness of its emission, the merging of circumstellar matter with the ambient ISM and the confusion from foreground and background interstellar hydrogen along the same line of sight. With the upgraded Nancay Radiotelescope, we have started a new search for HI at 21 cm towards AGB stars and post-AGBs, including PNs. We illustrate our results on one case, EP~Aqr, which shows that the contamination by interstellar emission must be treated with great care and discuss the prospects with the SKA. In order to sort out the genuine circumstellar HI emission from the interstellar one, it is necessary to map large areas of the sky (at all angular scales from sub-arcsec to degrees) with high spectral resolution, high sensitivity and a large dynamical range.

  4. Metal content monitoring in Hypericum perforatum pharmaceutical derivatives by atomic absorption and emission spectrometry.

    PubMed

    Gomez, María R; Soledad, Cerutti; Olsina, Roberto A; Silva, María F; Martínez, Luis D

    2004-02-18

    Metals have been investigated in different plant materials in order to establish their normal concentration range and consider their role in plants as part of human medicinal treatment. Metal monitoring as a pattern recognition method is a promising tool in the characterization and/or standardization of phytomedicines. In the present work measurable amounts of Ca, Cu, K, Li, Mg, Mn, Na, Ni, and Zn were detected in phytopharmaceutical derivatives of Hypericum perforatum by atomic techniques. Atomic methodologies like flame atomic absorption spectrometry (FAAS) and electrothermal atomic absorption spectrometry (ETAAS) allow reliable determination of mineral content in pharmaceutical quality control of medicinal plants. Additionally, capillary electrophoresis (CE) patterns of characteristic components (fingerprints) have been performed for the search of adulterants in phytopharmaceutical products. PMID:15127813

  5. Noise-immune cavity-enhanced analytical atomic spectrometry - NICE-AAS - A technique for detection of elements down to zeptogram amounts

    NASA Astrophysics Data System (ADS)

    Axner, Ove; Ehlers, Patrick; Hausmaninger, Thomas; Silander, Isak; Ma, Weiguang

    2014-10-01

    Noise-immune cavity-enhanced optical heterodyne molecular spectroscopy (NICE-OHMS) is a powerful technique for detection of molecular compounds in gas phase that is based on a combination of two important concepts: frequency modulation spectroscopy (FMS) for reduction of noise, and cavity enhancement, for prolongation of the interaction length between the light and the sample. Due to its unique properties, it has demonstrated unparalleled detection sensitivity when it comes to detection of molecular constituents in the gas phase. However, despite these, it has so far not been used for detection of atoms, i.e. for elemental analysis. The present work presents an assessment of the expected performance of Doppler-broadened (Db) NICE-OHMS for analytical atomic spectrometry, then referred to as noise-immune cavity-enhanced analytical atomic spectrometry (NICE-AAS). After a description of the basic principles of Db-NICE-OHMS, the modulation and detection conditions for optimum performance are identified. Based on a previous demonstrated detection sensitivity of Db-NICE-OHMS of 5 × 10- 12 cm- 1 Hz- 1/2 (corresponding to a single-pass absorbance of 7 × 10- 11 over 10 s), the expected limits of detection (LODs) of Hg and Na by NICE-AAS are estimated. Hg is assumed to be detected in gas phase directly while Na is considered to be atomized in a graphite furnace (GF) prior to detection. It is shown that in the absence of spectral interferences, contaminated sample compartments, and optical saturation, it should be feasible to detect Hg down to 10 zg/cm3 (10 fg/m3 or 10- 5 ng/m3), which corresponds to 25 atoms/cm3, and Na down to 0.5 zg (zg = zeptogram = 10- 21 g), representing 50 zg/mL (parts-per-sextillion, pps, 1:1021) in liquid solution (assuming a sample of 10 μL) or solely 15 atoms injected into the GF, respectively. These LODs are several orders of magnitude lower (better) than any previous laser-based absorption technique previously demonstrated under atmospheric

  6. Fast Excitation and Photon Emission of a Single-Atom-Cavity System

    SciTech Connect

    Bochmann, J.; Muecke, M.; Langfahl-Klabes, G.; Erbel, C.; Weber, B.; Specht, H. P.; Moehring, D. L.; Rempe, G.

    2008-11-28

    We report on the fast excitation of a single atom coupled to an optical cavity using laser pulses that are much shorter than all other relevant processes. The cavity frequency constitutes a control parameter that allows the creation of single photons in a superposition of two tunable frequencies. Each photon emitted from the cavity thus exhibits a pronounced amplitude modulation determined by the oscillatory energy exchange between the atom and the cavity. Our technique constitutes a versatile tool for future quantum networking experiments.

  7. Determination of aluminum and silicon in biological materials by inductively coupled plasma atomic emission spectrometry with electrothermal vaporization

    NASA Astrophysics Data System (ADS)

    Matusiewicz, Henryk; Barnes, Ramon M.

    An atomic emission spectrometric method is described for the determination of trace elements in microvolume samples especially of biological materials. Based upon the arrangement of a commercial electrothermal vaporizer and a 40-MHz inductively coupled plasma, the direct determination of aluminum and silicon in human body fluids such as urine and serum and aluminum in hemodialysis solution is performed. The instrumental system involves vaporizing the sample from a modified graphite electrode followed by atomization and excitation of the vapors in the ICP discharge. Compromise experimental conditions are reported and calibration functions compared. Limits of detection in 5-μl samples were 8 pg Al and 2.5 ng Si, and after preconcentration of Al with a poly(acrylamidoxime) resin, the detection limit was 1 pg Al. Recovery of 5 μg Si/ml and 10 ng Al/ml from aqueous and synthetic standards was 80-85% and 96-103%, respectively.

  8. Retrieval of thermospheric atomic oxygen, nitrogen and temperature from the 732 NM emission measured by the ISO on ATLAS 1

    NASA Technical Reports Server (NTRS)

    Fennelly, Judy A.; Torr, Douglas G.; Torr, Marsha R.; Richards, Phillip G.; Yung, Sopo

    1993-01-01

    The Imaging Spectrometric Observatory (ISO) was a part of the ATLAS 1 Mission flown on the shuttle Atlantis from March 24 to April 2, 1992. During limb scanning operations, the ISO measured the O+(2P) ion emission at 732 nm. We have used a numerical inversion technique to retrieve thermospheric atomic oxygen, molecular nitrogen and temperature profiles. These preliminary results indicate a lower thermospheric temperature cooler than that predicted by MSIS for the solar conditions during the mission. Although the densities agree at low altitudes, the reduced scale height produces O and N2 densities 25 percent lower than the MSIS at 300 km.

  9. New method for determining relative oscillator strengths of atoms through combined absorption and emission measurements - Application to titanium /Ti I/

    NASA Technical Reports Server (NTRS)

    Cardon, B. L.; Smith, P. L.; Whaling, W.

    1979-01-01

    The paper introduces a procedure that combines measurements of absorption and emission by atoms to obtain relative oscillator strengths that are independent of temperature determination in the sources and of assumptions regarding local thermodynamic equilibrium. The experimental observations are formed into sets of transitions and required to satisfy defined ratios. The procedure is illustrated with the published data of Whaling et al. and Smith and Kuehne for 16 transitions in Ti I. It is shown that the relative oscillator strengths resulting from this procedure have calculated uncertainties between 5 and 17% (about 95% confidence level). Evidence is presented to suggest that these uncertainties have been overestimated.

  10. Determination of rare earth elements in geological materials by inductively coupled argon plasma/atomic emission spectrometry

    USGS Publications Warehouse

    Crock, J.G.; Lichte, F.E.

    1982-01-01

    Inductively coupled argon plasma/optical emission spectrometery (ICAP/OES) is useful as a simultaneous, multielement analytical technique for the determination of trace elements in geological materials. A method for the determination of trace-level rare earth elements (REE) in geological materials using an ICAP 63-channel emission spectrometer is described. Separation and preconcentration of the REE and yttrium from a sample digest are achieved by a nitric acid gradient cation exchange and hydrochloric acid anion exchange. Precision of 1-4% relative standard deviation and comparable accuracy are demonstrated by the triplicate analysis of three splits of BCR-1 and BHVO-1. Analyses of other geological materials including coals, soils, and rocks show comparable precision and accuracy.

  11. Shape-dependent localized surface plasmon enhanced UV-emission from ZnO grown by atomic layer deposition

    NASA Astrophysics Data System (ADS)

    Lin, Ying; Liu, Xing Qiang; Wang, Ti; Chen, Chao; Wu, Hao; Liao, Lei; Liu, Chang

    2013-03-01

    Two-dimensional arrays of Al nanoparticles (NPs) were used to demonstrate the localized surface plasmon resonance (LSPR) enhanced UV light emission from ZnO grown by atomic layer deposition. Well defined NP arrays with different shapes were fabricated on the surface of ZnO by electron-beam lithography. A theoretical analysis based on the finite-difference time-domain method was carried out to show the shape dependence of the LSPR wavelength. Time resolved photoluminescence and temperature-dependent photoluminescence measurements suggested that the Al NPs arrays increase the radiative recombination rate by the resonance coupling between the localized surface plasmons and the excitons of the ZnO. By top excitation of the Al NP arrays coupled with ZnO, a 2.6-fold enhancement in peak photoluminescence intensity was measured. The enhancement strongly depended on the NP’s shape, revealing an important way of geometrical tuning the UV-emission.

  12. Shape-dependent localized surface plasmon enhanced UV-emission from ZnO grown by atomic layer deposition.

    PubMed

    Lin, Ying; Liu, Xing Qiang; Wang, Ti; Chen, Chao; Wu, Hao; Liao, Lei; Liu, Chang

    2013-03-29

    Two-dimensional arrays of Al nanoparticles (NPs) were used to demonstrate the localized surface plasmon resonance (LSPR) enhanced UV light emission from ZnO grown by atomic layer deposition. Well defined NP arrays with different shapes were fabricated on the surface of ZnO by electron-beam lithography. A theoretical analysis based on the finite-difference time-domain method was carried out to show the shape dependence of the LSPR wavelength. Time resolved photoluminescence and temperature-dependent photoluminescence measurements suggested that the Al NPs arrays increase the radiative recombination rate by the resonance coupling between the localized surface plasmons and the excitons of the ZnO. By top excitation of the Al NP arrays coupled with ZnO, a 2.6-fold enhancement in peak photoluminescence intensity was measured. The enhancement strongly depended on the NP's shape, revealing an important way of geometrical tuning the UV-emission. PMID:23466715

  13. Comment on ''Effect of entanglement on the decay dynamics of a pair of H(2p) atoms due to spontaneous emission''

    SciTech Connect

    Sancho, Pedro; Plaja, Luis

    2011-06-15

    T. Tanabe et al. [Phys. Rev. A 82, 040101(R) (2010)] have experimentally demonstrated that the emission properties of unstable atoms in entangled and product states are different. The authors define an apparent decay time as a fitting parameter which falls below the lifetime of the single atom for entangled pairs. We argue that their results about coincidence time spectra are correct, but those concerning lifetimes cannot be considered conclusive because they assume the emission of photons by the two atoms to be independent processes, a doubtful hypothesis for entangled states. We suggest an improved evaluation of the lifetimes based on a rigorous approach, which demands some modifications of the experimental procedure.

  14. A Coupled Chemistry-emission Model for Atomic Oxygen Green and Red-doublet Emissions in the Comet C/1996 B2 Hyakutake

    NASA Astrophysics Data System (ADS)

    Bhardwaj, Anil; Raghuram, Susarla

    2012-03-01

    The green (5577 Å) and red-doublet (6300, 6364 Å) lines are prompt emissions of metastable oxygen atoms in the 1 S and 1 D states, respectively, that have been observed in several comets. The value of the intensity ratio of green to red-doublet (G/R ratio) of 0.1 has been used as a benchmark to identify the parent molecule of oxygen lines as H2O. A coupled chemistry-emission model is developed to study the production and loss mechanisms of the O(1 S) and O(1 D) atoms and the generation of red and green lines in the coma of C/1996 B2 Hyakutake. The G/R ratio depends not only on photochemistry, but also on the projected area observed for cometary coma, which is a function of the dimension of the slit used and the geocentric distance of the comet. Calculations show that the contribution of photodissociation of H2O to the green (red) line emission is 30%-70% (60%-90%), while CO2 and CO are the next potential sources contributing 25%-50% (<5%). The ratio of the photoproduction rate of O(1 S) to O(1 D) would be around 0.03 (±0.01) if H2O is the main source of oxygen lines, whereas it is ~0.6 if the parent is CO2. Our calculations suggest that the yield of O(1 S) production in the photodissociation of H2O cannot be larger than 1%. The model-calculated radial brightness profiles of the red and green lines and G/R ratios are in good agreement with the observations made on the comet Hyakutake in 1996 March.

  15. A COUPLED CHEMISTRY-EMISSION MODEL FOR ATOMIC OXYGEN GREEN AND RED-DOUBLET EMISSIONS IN THE COMET C/1996 B2 HYAKUTAKE

    SciTech Connect

    Bhardwaj, Anil; Raghuram, Susarla E-mail: anil_bhardwaj@vssc.gov.in

    2012-03-20

    The green (5577 Angstrom-Sign ) and red-doublet (6300, 6364 Angstrom-Sign ) lines are prompt emissions of metastable oxygen atoms in the {sup 1}S and {sup 1}D states, respectively, that have been observed in several comets. The value of the intensity ratio of green to red-doublet (G/R ratio) of 0.1 has been used as a benchmark to identify the parent molecule of oxygen lines as H{sub 2}O. A coupled chemistry-emission model is developed to study the production and loss mechanisms of the O({sup 1}S) and O({sup 1}D) atoms and the generation of red and green lines in the coma of C/1996 B2 Hyakutake. The G/R ratio depends not only on photochemistry, but also on the projected area observed for cometary coma, which is a function of the dimension of the slit used and the geocentric distance of the comet. Calculations show that the contribution of photodissociation of H{sub 2}O to the green (red) line emission is 30%-70% (60%-90%), while CO{sub 2} and CO are the next potential sources contributing 25%-50% (<5%). The ratio of the photoproduction rate of O({sup 1} S) to O({sup 1} D) would be around 0.03 ({+-}0.01) if H{sub 2}O is the main source of oxygen lines, whereas it is {approx}0.6 if the parent is CO{sub 2}. Our calculations suggest that the yield of O({sup 1} S) production in the photodissociation of H{sub 2}O cannot be larger than 1%. The model-calculated radial brightness profiles of the red and green lines and G/R ratios are in good agreement with the observations made on the comet Hyakutake in 1996 March.

  16. High angular resolution measurements of K shell x-ray emission created by electron channeling in the analytical electron microscope.

    SciTech Connect

    Zaluzec, N. J.

    1999-03-10

    Since the original observations by Duncumb in 1962, a number of studies have been conducted on the effects of electron channel on characteristic x-ray emission and microanalysis. Most of the recent studies have concentrated upon using the phenomenon to perform site specific distributions of impurity elements in ordered compounds using the ALCHEMI methodology. Very few studies have attempted to accurately measure the effect as a function of orientation and compare these results to theories. In this study, two dimensional high angular resolution studies of channeling enhance x-ray emission were performed and herein the results are compared to theoretical calculations of Allen et al. All experimental measurements presented here were conducted on a Philips EM 420T analytical electron microscope. The instrument was operated in the TEM mode, at 120 kV using an LaB6 electron source. The characteristic x-ray emission was measured using an EDAX ultra thin window Si(Li) detector having a FWHM of {approximately}145 eV at Mn Km Nominal probe sizes used during the study were 200-500 nm with beam convergence half angle defined by the Condenser apertures. Control of the relative orientation of the incident probe was accomplished via direct computer control of the beam tilt coils, after the specimen was first manually oriented to an appropriate zone axis using the specimen tilt stage. Two dimensional measurements were carried out using a 128 x 100 pixel scan corresponding to an angular range of {approximately}100 by 80 mR using customized computer program running on a EDAX 9900 microanalyzer system. Careful alignment and manual optimization/adjustments of beam tilt pivot coils, minimized probe wobble during data acquisition. The effects of this were additionally mitigated due to the relative uniformity of the specimen thickness in the analyzed zone. Typical acquisition times for a complete two dimensional scan were 18-24 hours. Essential to the success of these measurements was

  17. Atomically precise doping of monomanganese ion into coreless supertetrahedral chalcogenide nanocluster inducing unusual red shift in Mn(2+) emission.

    PubMed

    Lin, Jian; Zhang, Qian; Wang, Le; Liu, Xiaochun; Yan, Wenbo; Wu, Tao; Bu, Xianhui; Feng, Pingyun

    2014-03-26

    We report a simple and yet effective method to introduce Mn(2+) ions into semiconducting nanoclusters with atomically precise control. Our method utilizes one type of micrometer-sized crystals, composed of well-defined isolated supertetrahedral chalcogenide nanoclusters (∼2 nm, [Cd6In28S52(SH)4]) whose core metal site is unoccupied in as-synthesized pristine form. This unique model structure with vacant core site makes it possible to achieve ordered distribution of Mn(2+) dopants, and at the same time effectively preclude the formation of Mn(2+) clusters in the host matrix. A two-step synthesis strategy is applied to realize an atomically precise doping of Mn(2+) ion into the core site of the nanoclusters, and to achieve uniform distribution of Mn(2+) dopants in the crystal lattice. The PL, X-ray photoelectron (XPS), as well as the electron paramagnetic resonance (EPR) spectra reveal the successful incorporation of Mn(2+) ion into the core site of the nanocluster. Different from the pristine host material with weak green emission (∼490 nm), the Mn(2+)-doped material shows a strong red emission (630 nm at room temperature and 654 nm at 30 K), which is significantly red-shifted relative to the orange emission (∼585 nm) observed in traditional Mn(2+)-doped II-VI semiconductors. Various experiments including extensive synthetic variations and PL dynamics have been performed to probe the mechanistic aspects of synthesis process and resultant unusual structural and PL properties. The quaternary semiconductor material reported here extends the emission window of Mn(2+)-doped II-VI semiconductor from yellow-orange to red, opening up new opportunities in applications involving photonic devices and bioimaging.

  18. Ultrafast emission of ions during laser ablation of metal for 3D atom probe

    NASA Astrophysics Data System (ADS)

    Vella, A.; Houard, J.; Vurpillot, F.; Deconihout, B.

    2009-03-01

    The 3D atom probe(3DAP) is an imaging instrument based on the controlled field evaporation of single atoms from a sample having a tip shape with an end radius of 50 nm. In the fs laser assisted 3DAP the evaporation is induced by the laser pulses so that the physical process involved in this 3DAP analysis might correspond to the very early stages of the ablation process. In this paper we present the principle of the 3DAP and we discuss the existing models of the fs assisted evaporation. At last, we test the relevance of these models with pump-probe experiments on tungsten tips in the tomographic atom probe.

  19. Acoustic emission and magnification of atomic lines resolution for laser breakdown of salt water in ultrasound field

    SciTech Connect

    Bulanov, Alexey V.; Nagorny, Ivan G.

    2015-10-28

    Researches of the acoustic effects accompanying optical breakdown in a water, generated by the focused laser radiation with power ultrasound have been carried out. Experiments were performed by using 532 nm pulses from Brilliant B Nd:YAG laser. Acoustic radiation was produced by acoustic focusing systems in the form hemisphere and ring by various resonance frequencies of 10.7 kHz and 60 kHz. The experimental results are obtained, that show the sharply strengthens effects of acoustic emission from a breakdown zone by the joint influence of a laser and ultrasonic irradiation. Essentially various thresholds of breakdown and character of acoustic emission in fresh and sea water are found out. The experimental result is established, testifying that acoustic emission of optical breakdown of sea water at presence and at absence of ultrasound essentially exceeds acoustic emission in fresh water. Atomic lines of some chemical elements like a Sodium, Magnesium and so on were investigated for laser breakdown of water with ultrasound field. The effect of magnification of this lines resolution for salt water in ultrasound field was obtained.

  20. Separation and preconcentration of ultra trace amounts of beryllium in water samples using mixed micelle-mediated extraction and determination by inductively coupled plasma-atomic emission spectrometry.

    PubMed

    Beiraghi, Assadollah; Babaee, Saeed

    2008-01-28

    In the present study a cloud point extraction process using mixed micelle of the cationic surfactant cetyl-pyridinium chloride (CPC) and non-ionic surfactant Triton X-114 for extraction of beryllium from aqueous solutions is developed. The extraction of analyte from aqueous samples was performed in the presence of 1,8-dihydroxyanthrone as chelating agent in buffer media of pH 9.5. After phase separation, the surfactant-rich phase was diluted with 0.4mL of a 60:40 methanol-water mixture containing 0.03 mL HNO(3). Then, the enriched analyte in the surfactant-rich phase was determined by inductively coupled plasma-atomic emission spectrometry (ICP-AES). The different variables affecting the complexation and extraction conditions were optimized. Under the optimum conditions (i.e. 1.6 x 10(-4) molL(-1) 1,8-dihydroxyanthrone, 1.2 x 10(-4) molL(-1) CPC, 0.15% (v/v) Triton X-114, 50 degrees C equilibrium temperature) the calibration graph was linear in the range of 0.006-80 ngmL(-1) with detection limit of 0.001 ngmL(-1) and the precision (R.S.D.%) for five replicate determinations at 18 ngmL(-1) of Be(II) was better than 2.9%. In this manner the preconcentration and enrichment factors were 16.7 and 24.8, respectively. Under the presence of foreign ions no significant interference was observed. Finally, the proposed method was successfully utilized for the determination of this cation in water samples.

  1. Effect of surfactant addition on ultrasonic leaching of trace elements from plant samples in inductively coupled plasma-atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Borkowska-Burnecka, Jolanta; Jankowiak, Urszula; Zyrnicki, Wieslaw; Anna Wilk, Kazimiera

    2004-04-01

    The applicability of surfactants in sample preparation of plant materials followed by analysis by inductively coupled plasma atomic emission spectrometry has been examined. Reference materials (INCT-MPH-2-Mixed Polish Herbs, INCT-TL-1 black tea leaves and CTA-VTL-2 -Virginia tobacco leaves) and commercially available tea leaves were analyzed. Effects of addition surfactants (Triton X-100, didodecyldimethylammonium bromide and cetyltrimethylammonium bromide) on efficiency of ultrasonic leaching of elements from the plant samples and on plasma parameters were investigated. Low concentrations of the surfactants in solutions did not affect, in practice, analytical line intensities and the nebulization process. Quantitative recovery of some elements could be obtained by ultrasonic diluted acid leaching with the aid of surfactants. However, the element recovery depended on type of surfactant, as well as element and sample material. Plasma parameters, i.e. the excitation temperatures of Ar I, Fe II and Ca II as well as the electron number density and the Mg II/Mg I intensity ratio did not vary significantly due to the surfactants in solutions.

  2. Evaluation of a direct injection nebulizer interface for flow injection analysis and high performance liquid chromatography with inductively coupled plasma-atomic emission spectroscopic detection

    SciTech Connect

    LaFreniere, K.E.

    1986-06-01

    A direct injection nebulizer (DIN) was designed, developed, and evaluated to determine its potential utilization as an effective interface for flow injection analysis (FIA) and high performance liquid chromatography (HPLC) coupled with inductively coupled plasma-atomic emission spectroscopic detection. The analytical figures of merit for the DIN when used as an interface for FIA-ICP-AES were found to be comparable to or better than those obtained with conventional pneumatic nebulization in terms of limits of detection (LODs), reproducibility, linearity, and interelement effects. Stable plasma operation was maintained for the DIN sample introduction of a variety of pure organic solvents, including acetonitrile, methanol, methylisobutylketone, and pyridine. The HPLC-DIN-ICP-AES facility was specifically applied for the speciation of inorganic and organometallic species contained in synthetic mixtures, vanilla extracts, and a variety of energy-related materials, such as shale oil process water, coal extracts, shale oil, crude oil, and an SRC II. Suggestions for future research are also considered. 227 refs., 44 figs., 15 tabs.

  3. Evaluation of a direct injection nebulizer interface for flow injection analysis and high performance liquid chromatography with inductively coupled plasma-atomic emission spectroscopic detection

    SciTech Connect

    LaFreniere, K.E.

    1986-01-01

    A direct injection nebulizer (DIN) was designed, developed and evaluated to determine its potential utilization as an effective interface for flow injection analysis (FIA) and high performance liquid chromatography (HPLC) coupled with inductively coupled plasma-atomic emission spectroscopic detection. The analytical figures of merit for the DIN when used as an interface for FIA-ICP-AES were found to be comparable to or better than those obtained with conventional pneumatic nebulization in terms of limits of detection (LODs), reproducibility, linearity, and interelement effects. In the HPLC mode, the LODDs were found to be comparable to those obtained by continuous-flow sample introduction into the ICP, or inferior by up to only a factor of four. Stable plasma operation was maintained for the DIN sample introduction of a variety of pure organic solvents, including acetonitrile, methanol, methyl-isobutylketone, and pyridine. The HPLC-DIN-ICP-AES facility was specifically applied for the speciation of inorganic and organo-metallic species contained in synthetic mixtures, vanilla extracts and a variety of energy-related materials, such as shale oil process water, coal extracts, shale oil, crude oil, and an SRC II. Suggestions for future research are also considered.

  4. Determination of gaseous semi- and low-volatile organic halogen compounds by barrier-discharge atomic emission spectrometry.

    PubMed

    Sun, Yifei; Watanabe, Nobuhisa; Wang, Wei; Zhu, Tianle

    2013-01-01

    A group parameter approach using "total organic halogen" is effective for monitoring gaseous organic halogen compounds, including fluorine, chlorine, and bromine compounds, generated from combustion. We described the use of barrier-discharge radiofrequency-helium-plasma/atomic emission spectrometry, for the detection of semi- and low-volatile organic halogen compounds (SLVOXs), which can be collected by Carbotrap adsorbents and analyzed using thermal desorption. The optimal carrier gas flow rates at the injection and desorption lines were established to be 100 mL/min. The detection range for SLVOXs in the gaseous samples was from 10 ng to tens of micrograms. Measuring F was more difficult than measuring C1 or Br, because the wavelength of F is close to that of air. The barrier-discharge radiofrequency-helium-plasma/atomic emission spectrometry measured from 85% to 103% of the SLVOXs in the gas sample. It has been found that Carbotrap B is appropriate for high-boiling-point compounds, and Carbotrap C is suitable for the determination of organic halogen compounds with lower boiling points, in the range 200-2300C. Under optimal analysis conditions, a chlorine-containing plastic was destroyed using different oxygen concentrations. Lower oxygen concentrations resulted in the production of lower amounts of organic halogen compounds. PMID:23586317

  5. CHIANTI-AN ATOMIC DATABASE FOR EMISSION LINES. XIII. SOFT X-RAY IMPROVEMENTS AND OTHER CHANGES

    SciTech Connect

    Landi, E.; Young, P. R.; Dere, K. P.; Del Zanna, G.; Mason, H. E.

    2013-02-15

    The CHIANTI spectral code consists of two parts: an atomic database and a suite of computer programs in Python and IDL. Together, they allow the calculation of the optically thin spectrum of astrophysical objects and provide spectroscopic plasma diagnostics for the analysis of astrophysical spectra. The database includes atomic energy levels, wavelengths, radiative transition probabilities, collision excitation rate coefficients, ionization, and recombination rate coefficients, as well as data to calculate free-free, free-bound, and two-photon continuum emission. Version 7.1 has been released, which includes improved data for several ions, recombination rates, and element abundances. In particular, it provides a large expansion of the CHIANTI models for key Fe ions from Fe VIII to Fe XIV to improve the predicted emission in the 50-170 A wavelength range. All data and programs are freely available at http://www.chiantidatabase.org and in SolarSoft, while the Python interface to CHIANTI can be found at http://chiantipy.sourceforge.net.

  6. Miniaturized dielectric barrier discharge carbon atomic emission spectrometry with online microwave-assisted oxidation for determination of total organic carbon.

    PubMed

    Han, Bingjun; Jiang, Xiaoming; Hou, Xiandeng; Zheng, Chengbin

    2014-07-01

    A simple, rapid, and portable system consisted of a laboratory-built miniaturized dielectric barrier discharge atomic emission spectrometer and a microwave-assisted persulfate oxidation reactor was developed for sensitive flow injection analysis or continuous monitoring of total organic carbon (TOC) in environmental water samples. The standard/sample solution together with persulfate was pumped to the reactor to convert organic compounds to CO2, which was separated from liquid phase and transported to the spectrometer for detection of the elemental specific carbon atomic emission at 193.0 nm. The experimental parameters were systematically investigated. A limit of detection of 0.01 mg L(-1) (as C) was obtained based on a 10 mL sample injection volume, and the precision was better than 6.5% (relative standard deviation, RSD) at 0.1 mg L(-1). The system was successfully applied for TOC analysis of real environmental water samples. The obtained TOC value of 30 test samples agreed well with those by the standard high-temperature combustion coupled nondispersive infrared absorption method. Most importantly, the system showed good capability of in situ continuous monitoring of total organic carbon in environmental water.

  7. Determination of gaseous semi- and low-volatile organic halogen compounds by barrier-discharge atomic emission spectrometry.

    PubMed

    Sun, Yifei; Watanabe, Nobuhisa; Wang, Wei; Zhu, Tianle

    2013-01-01

    A group parameter approach using "total organic halogen" is effective for monitoring gaseous organic halogen compounds, including fluorine, chlorine, and bromine compounds, generated from combustion. We described the use of barrier-discharge radiofrequency-helium-plasma/atomic emission spectrometry, for the detection of semi- and low-volatile organic halogen compounds (SLVOXs), which can be collected by Carbotrap adsorbents and analyzed using thermal desorption. The optimal carrier gas flow rates at the injection and desorption lines were established to be 100 mL/min. The detection range for SLVOXs in the gaseous samples was from 10 ng to tens of micrograms. Measuring F was more difficult than measuring C1 or Br, because the wavelength of F is close to that of air. The barrier-discharge radiofrequency-helium-plasma/atomic emission spectrometry measured from 85% to 103% of the SLVOXs in the gas sample. It has been found that Carbotrap B is appropriate for high-boiling-point compounds, and Carbotrap C is suitable for the determination of organic halogen compounds with lower boiling points, in the range 200-2300C. Under optimal analysis conditions, a chlorine-containing plastic was destroyed using different oxygen concentrations. Lower oxygen concentrations resulted in the production of lower amounts of organic halogen compounds.

  8. Density profiles of atoms in nano-tubes from an analytic method: hydrogen in a cylindrical pore

    NASA Astrophysics Data System (ADS)

    Boublík, Tomáš

    2011-01-01

    Knowledge of the structure of simple fluids in nano-tubes constitutes important information in many scientific and technical branches. Computer simulations and density functional theory (DFT) offer accurate but laborious results. We have proposed a simple analytical method to determine the background correlation function on the basis of the residual chemical potentials of a pair of interacting bodies and of the corresponding combined body. These potentials are obtained in terms of geometric quantities. In this paper we dealt with the combination rule for the geometric quantity Q; the harmonic mean rule was proposed and verified at low densities by calculating the third cross-virial coefficient, and by comparing calculated density profiles of the inhomogeneous systems of hard sphere-wall at higher densities. A slight improvement over the previous results were found. Next, we applied our analytic method to realistic systems of a simple molecule in the graphite cylindrical pore. Hydrogen (and carbon monoxide), interacting with carbon of the graphite via the modified LJ potential are considered and the density profile was determined taking into account only the soft-sphere interaction within Weeks-Chandler-Andersen approximation. The considered approach was found to yield a fair description of the realistic simple fluid-cylindrical pore system.

  9. Electron emission in slow collisions of inert gas and reactive ions with W(110) partially covered by alkali atoms

    NASA Astrophysics Data System (ADS)

    Müller, H.; Hausmann, R.; Brenten, H.; Kempter, V.

    1993-05-01

    Electron energy spectra from slow (50 to 1000 eV) collisions of inert gas (He +, He 2+ and Ar +) and reactive (H +, N +) ions colliding under grazing incidence with W(110) surfaces are reported. The surface work function is varied by the exposure of the W(110) surface to alkali atoms. For clean W(110) the sequence of electronic transitions during a slow (50 eV, typically) collision is similar as reported for other clean metals: Auger capture processes involving two electrons from the surface dominate for all projectiles. For sufficiently large coverages by alkali atoms resonant capture of one or two surface electrons by the projectiles leads to the formation of excited states of the projectiles with one or two electrons occupying valence orbitals. These states decay by Auger deexcitation (Penning ionization) and intra-atomic Auger processes (autoionization and autodetachment), respectively. For the case of Ar + ions colliding with W(110) partially covered by potassium it is demonstrated that core vacancies (Ar3p -1) are created during the collision provided the kinetic energy of the projectile surmounts about 300 eV. Contributions from both potential and kinetic emission can then be seen in the spectra of the emitted electrons.

  10. Research as a guide for curriculum development: An example from introductory spectroscopy. II. Addressing student difficulties with atomic emission spectra

    NASA Astrophysics Data System (ADS)

    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.

  11. Research as a guide for curriculum development: An example from introductory spectroscopy. I. Identifying student difficulties with atomic emission spectra

    NASA Astrophysics Data System (ADS)

    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.

  12. Post sunset behavior of the 6300 A atomic oxygen airglow emission

    NASA Technical Reports Server (NTRS)

    Smith, R. E.

    1976-01-01

    A theoretical model of the 6300 A OI airglow emission was developed based on the assumptions that both the charged and neutral portions of the Earth's upper atmosphere are in steady state conditions of diffusive equilibrium. Intensities of 6300 A OI emission line were calculated using electron density true height profiles from a standard C-4 ionosonde and exospheric temperatures derived from Fabry-Perot interferometer measurements of the Doppler broadened 6300 A emission line shape as inputs to the model. Reaction rate coefficient values, production mechanism efficiencies, solar radiation fluxes, absorption cross sections, and models of the neutral atmosphere were varied parametrically to establish a set of acceptable inputs which will consistently predict 6300 A emission intensities that closely agree with intensities observed during the post-sunset twilight period by an airglow observatory consisting of a Fabry-Perot interferometer and a turret photometer. Emission intensities that can only result from the dissociative recombination of molecular oxygen ions were observed during the latter portion of the observational period. Theoretical calculations indicate that contamination of the 6300 A OI emission should be on the order of or less than 3 percent; however, these results are very sensitive to the wavelengths of the individual lines and their intensities relative to the 6300 A OI intensity. This combination of a model atmosphere, production mechanism efficiencies, and quenching coefficient values was used when the dissociative photoexcitation and direct impact excitation processes were contributing to the intensity to establish best estimates of solar radiation fluxes in the Schumann--Runge continuum and associated absorption cross sections. Results show that the Jacchia 1971 model of the upper atmosphere combined with the Ackerman recommended solar radiation fluxes and associated absorption cross sections produces theoretically calculated intensities that more

  13. Characterization of Homogeneous, Cooperative Protein-DNA Clusters by Sedimentation Equilibrium Analytical Ultracentrifugation and Atomic Force Microscopy.

    PubMed

    Tessmer, Ingrid; Fried, Michael G

    2015-01-01

    Strong, positively cooperative binding can lead to the clustering of proteins on DNA. Here, we describe one approach to the analysis of such clusters. Our example is based on recent studies of the interactions of O(6)-alkylguanine DNA alkyltransferase (AGT) with high-molecular-weight DNAs (Adams et al., 2009; Tessmer, Melikishvili, & Fried, 2012). Cooperative cluster size distributions are predicted using the simplest homogeneous binding and cooperativity (HBC) model, together with data obtained by sedimentation equilibrium analysis. These predictions are tested using atomic force microscopy imaging; for AGT, measured cluster sizes are found to be significantly smaller than those predicted by the HBC model. A mechanism that may account for cluster size limitation is briefly discussed.

  14. Characterization of Homogeneous, Cooperative Protein-DNA Clusters by Sedimentation Equilibrium Analytical Ultracentrifugation and Atomic Force Microscopy.

    PubMed

    Tessmer, Ingrid; Fried, Michael G

    2015-01-01

    Strong, positively cooperative binding can lead to the clustering of proteins on DNA. Here, we describe one approach to the analysis of such clusters. Our example is based on recent studies of the interactions of O(6)-alkylguanine DNA alkyltransferase (AGT) with high-molecular-weight DNAs (Adams et al., 2009; Tessmer, Melikishvili, & Fried, 2012). Cooperative cluster size distributions are predicted using the simplest homogeneous binding and cooperativity (HBC) model, together with data obtained by sedimentation equilibrium analysis. These predictions are tested using atomic force microscopy imaging; for AGT, measured cluster sizes are found to be significantly smaller than those predicted by the HBC model. A mechanism that may account for cluster size limitation is briefly discussed. PMID:26412659

  15. Spontaneous light emission by atomic hydrogen: Fermi's golden rule without cheating

    NASA Astrophysics Data System (ADS)

    Debierre, V.; Durt, T.; Nicolet, A.; Zolla, F.

    2015-10-01

    Focusing on the 2 p- 1 s transition in atomic hydrogen, we investigate through first order perturbation theory the time evolution of the survival probability of an electron initially taken to be in the excited (2 p) state. We examine both the results yielded by the standard dipole approximation for the coupling between the atom and the electromagnetic field - for which we propose a cutoff-independent regularisation - and those yielded by the exact coupling function. In both cases, Fermi's golden rule is shown to be an excellent approximation for the system at hand: we found its maximal deviation from the exact behaviour of the system to be of order 10-8 /10-7. Our treatment also yields a rigorous prescription for the choice of the optimal cutoff frequency in the dipole approximation. With our cutoff, the predictions of the dipole approximation are almost indistinguishable at all times from the exact dynamics of the system.

  16. Improved statistical determination of absolute neutrino masses via radiative emission of neutrino pairs from atoms

    NASA Astrophysics Data System (ADS)

    Zhang, Jue; Zhou, Shun

    2016-06-01

    The atomic transition from an excited state |e ⟩ to the ground state |g ⟩ by emitting a neutrino pair and a photon, i.e., |e ⟩→|g ⟩+|γ ⟩+|νi⟩+|ν¯j⟩ with i , j =1 , 2, 3, has been proposed by Yoshimura and his collaborators as an alternative way to determine the absolute scale m0 of neutrino masses. More recently, a statistical analysis of the fine structure of the photon spectrum from this atomic process has been performed [N. Song et al. Phys. Rev. D 93, 013020 (2016)] to quantitatively examine the experimental requirements for a realistic determination of absolute neutrino masses. In this paper, we show how to improve the statistical analysis and demonstrate that the previously required detection time can be reduced by one order of magnitude for the case of a 3 σ determination of m0˜0.01 eV with an accuracy better than 10%. Such an improvement is very encouraging for further investigations on measuring absolute neutrino masses through atomic processes.

  17. Solar-energy conversion and light emission in an atomic monolayer p-n diode.

    PubMed

    Pospischil, Andreas; Furchi, Marco M; Mueller, Thomas

    2014-04-01

    The limitations of the bulk semiconductors currently used in electronic devices-rigidity, heavy weight and high costs--have recently shifted the research efforts to two-dimensional atomic crystals such as graphene and atomically thin transition-metal dichalcogenides. These materials have the potential to be produced at low cost and in large areas, while maintaining high material quality. These properties, as well as their flexibility, make two-dimensional atomic crystals attractive for applications such as solar cells or display panels. The basic building blocks of optoelectronic devices are p-n junction diodes, but they have not yet been demonstrated in a two-dimensional material. Here, we report a p-n junction diode based on an electrostatically doped tungsten diselenide (WSe2) monolayer. We present applications as a photovoltaic solar cell, a photodiode and a light-emitting diode, and obtain light-power conversion and electroluminescence efficiencies of ∼ 0.5% and ∼ 0.1%, respectively. Given recent advances in the large-scale production of two-dimensional crystals, we expect them to profoundly impact future developments in solar, lighting and display technologies.

  18. Solar-energy conversion and light emission in an atomic monolayer p-n diode

    NASA Astrophysics Data System (ADS)

    Pospischil, Andreas; Furchi, Marco M.; Mueller, Thomas

    2014-04-01

    The limitations of the bulk semiconductors currently used in electronic devices--rigidity, heavy weight and high costs--have recently shifted the research efforts to two-dimensional atomic crystals such as graphene and atomically thin transition-metal dichalcogenides. These materials have the potential to be produced at low cost and in large areas, while maintaining high material quality. These properties, as well as their flexibility, make two-dimensional atomic crystals attractive for applications such as solar cells or display panels. The basic building blocks of optoelectronic devices are p-n junction diodes, but they have not yet been demonstrated in a two-dimensional material. Here, we report a p-n junction diode based on an electrostatically doped tungsten diselenide (WSe2) monolayer. We present applications as a photovoltaic solar cell, a photodiode and a light-emitting diode, and obtain light-power conversion and electroluminescence efficiencies of ~0.5% and ~0.1%, respectively. Given recent advances in the large-scale production of two-dimensional crystals, we expect them to profoundly impact future developments in solar, lighting and display technologies.

  19. Solar-energy conversion and light emission in an atomic monolayer p-n diode.

    PubMed

    Pospischil, Andreas; Furchi, Marco M; Mueller, Thomas

    2014-04-01

    The limitations of the bulk semiconductors currently used in electronic devices-rigidity, heavy weight and high costs--have recently shifted the research efforts to two-dimensional atomic crystals such as graphene and atomically thin transition-metal dichalcogenides. These materials have the potential to be produced at low cost and in large areas, while maintaining high material quality. These properties, as well as their flexibility, make two-dimensional atomic crystals attractive for applications such as solar cells or display panels. The basic building blocks of optoelectronic devices are p-n junction diodes, but they have not yet been demonstrated in a two-dimensional material. Here, we report a p-n junction diode based on an electrostatically doped tungsten diselenide (WSe2) monolayer. We present applications as a photovoltaic solar cell, a photodiode and a light-emitting diode, and obtain light-power conversion and electroluminescence efficiencies of ∼ 0.5% and ∼ 0.1%, respectively. Given recent advances in the large-scale production of two-dimensional crystals, we expect them to profoundly impact future developments in solar, lighting and display technologies. PMID:24608229

  20. An analytical continuation approach for evaluating emission lineshapes of molecular aggregates and the adequacy of multichromophoric Förster theory

    NASA Astrophysics Data System (ADS)

    Banchi, Leonardo; Costagliola, Gianluca; Ishizaki, Akihito; Giorda, Paolo

    2013-05-01

    In large photosynthetic chromophore-protein complexes not all chromophores are coupled strongly, and thus the situation is well described by formation of delocalized states in certain domains of strongly coupled chromophores. In order to describe excitation energy transfer among different domains without performing extensive numerical calculations, one of the most popular techniques is a generalization of Förster theory to multichromophoric aggregates (generalized Förster theory) proposed by Sumi [J. Phys. Chem. B 103, 252 (1999), 10.1021/jp983477u] and Scholes and Fleming [J. Phys. Chem. B 104, 1854 (2000), 10.1021/jp993435l]. The aim of this paper is twofold. In the first place, by means of analytic continuation and a time convolutionless quantum master equation approach, a theory of emission lineshape of multichromophoric systems or molecular aggregates is proposed. In the second place, a comprehensive framework that allows for a clear, compact, and effective study of the multichromophoric approach in the full general version proposed by Jang, Newton, and Silbey [Phys. Rev. Lett. 92, 218301 (2004), 10.1103/PhysRevLett.92.218301] is developed. We apply the present theory to simple paradigmatic systems and we show on one hand the effectiveness of time-convolutionless techniques in deriving lineshape operators and on the other hand we show how the multichromophoric approach can give significant improvements in the determination of energy transfer rates in particular when the systems under study are not the purely Förster regime. The presented scheme allows for an effective implementation of the multichromophoric Förster approach which may be of use for simulating energy transfer dynamics in large photosynthetic aggregates, for which massive computational resources are usually required. Furthermore, our method allows for a systematic comparison of multichromophoric Föster and generalized Förster theories and for a clear understanding of their respective limits

  1. Efficient field emission from α-Fe2O3 nanoflakes on an atomic force microscope tip

    NASA Astrophysics Data System (ADS)

    Zhu, Y. W.; Yu, T.; Sow, C. H.; Liu, Y. J.; Wee, A. T. S.; Xu, X. J.; Lim, C. T.; Thong, J. T. L.

    2005-07-01

    Aligned arrays of flake-shaped hematite (α-Fe2O3) nanostructure have been fabricated on an atomic force microscope (AFM) tip. They are created by simply heating an iron-coated AFM tip in ambience on a hot plate. These nanoflakes are characterized as α-Fe2O3 single crystalline structures with tip radii as small as several nanometers and are highly effective as electron field emitters. With a vacuum gap of about 150μm, field emission measurements of α-Fe2O3 nanoflakes on AFM tips show a low turn-on voltage of about 400-600V and a high current density of 1.6Acm-2 under 900V. Such high emission current density is attributed to the nanoscale sharp tips of the as-grown nanoflakes. Based on the Fowler-Nordheim theory, it is demonstrated the enhancement factor of α-Fe2O3 nanoflakes on AFM tips is comparable to that of carbon nanotubes. Our findings suggest that α-Fe2O3 nanoflakes are potentially useful as candidates for future electron field emission devices.

  2. Analytical and experimental investigation of the feasibility of accelerated lifetime testing of materials exposed to an atomic oxygen beam

    NASA Technical Reports Server (NTRS)

    Albridge, Royal; Barnes, Alan; Tolk, Norman

    1993-01-01

    The interaction of atomic particles with surfaces is of both scientific and technological interest. Past work emphasizes the measurement of high-energy sputtering yields. Very little work utilized low-energy beams for which chemical and electronic effects can be important. Even less work has been carried out using well-defined low-energy projectiles. The use of low-energy, reactive projectiles permits one to investigate surface processes that have not been well characterized. As the energy of the projectile decreases, the collisional cascades and spikes, that are common for high-energy projectiles, become less important, and chemical and electronic effects can play a significant role. Aspects of particle-surface interactions are of concern in several areas of technology. For example, the erosion, desorption, and glow of surfaces of spacecraft in orbit are important in the arena of space technology. The materials studied under this contract are of possible use on the exterior portions of the power generation system of Space Station Freedom. Under the original designs, Space Station Freedom's power generation system would generate potential differences on the surface as high as 200 volts. Ions in the plasma that often surround orbiting vehicles would be accelerated by these potentials leading to bombardment and erosion of the exposed surfaces. The major constituent of the atmosphere, approximately 90 percent, in the low earth orbit region is atomic oxygen. Since atomic oxygen is extremely reactive with most materials, chemical effects can arise in addition to the physical sputtering caused by the acceleration of the oxygen ions. Furthermore, the incident oxygen ions can remain embedded in the exposed surfaces, altering the chemical composition of the surfaces. Since the effective binding energy of a chemically altered surface can be quite different from that of the pure substrate, the sputtering yield of a chemically altered surface is usually different also. The low

  3. Comparison of several spray chambers operating at very low liquid flow rates in inductively coupled plasma atomic emission spectrometry.

    PubMed

    Todolí, J L; Maestre, S; Mora, J; Canals, A; Hernandis, V

    2000-12-01

    Four different spray chambers were evaluated in ICP-AES at very low liquid flow rates: a double-pass (Scott type), a conventional cyclonic, and two low-volume cyclonic-type spray chambers (i.e., Cinnabar and Genie). A glass concentric pneumatic micro nebulizer (Atom Mist) was used in conjunction with all four chambers. The liquid flow rate was varied from 10 to 160 microL min(-1). The conventional cyclonic spray chamber gave rise to coarser tertiary aerosols, higher analyte and solvent transport rates, higher sensitivity and lower limits of detection than the remaining ones. The low-volume spray chambers afforded analytical figures of merit similar to the double-pass one, despite their very different designs. However, these spray chambers exhibited shorter wash-out times. The matrix effects were significant only for the double-pass. This fact allowed the analysis of reference samples by employing aqueous standards at a minimum level of sample consumption. The recoveries obtained for the cyclonic spray chambers and several certified samples were close to 100%, being always lower in the case of the double-pass spray chamber.

  4. Solid state effects in electron emission from atomic collisions near surfaces

    SciTech Connect

    Reinhold, C.O.; Burgdoerfer, J.; Minniti, R.; Elston, S.B.

    1996-10-01

    We present a brief progress report of recent studies of the ejected electron spectra arising from glancing-angle ion-surface scattering involving collision energies of hundreds of keV/u. A broad range of electron energies and emission angles is analyzed containing prominent structures such as the convoy electron peak and the binary ridge. Particular emphasis is placed on the search for signatures of dynamic image interactions and multiple scattering near surfaces. 30 refs., 8 figs.

  5. A Green Analytical Method Using Ultrasound in Sample Preparation for the Flow Injection Determination of Iron, Manganese, and Zinc in Soluble Solid Samples by Flame Atomic Absorption Spectrometry

    PubMed Central

    Yebra, M. Carmen

    2012-01-01

    A simple and rapid analytical method was developed for the determination of iron, manganese, and zinc in soluble solid samples. The method is based on continuous ultrasonic water dissolution of the sample (5–30 mg) at room temperature followed by flow injection flame atomic absorption spectrometric determination. A good precision of the whole procedure (1.2–4.6%) and a sample throughput of ca. 25 samples h–1 were obtained. The proposed green analytical method has been successfully applied for the determination of iron, manganese, and zinc in soluble solid food samples (soluble cocoa and soluble coffee) and pharmaceutical preparations (multivitamin tablets). The ranges of concentrations found were 21.4–25.61 μg g−1 for iron, 5.74–18.30 μg g−1 for manganese, and 33.27–57.90 μg g−1 for zinc in soluble solid food samples and 3.75–9.90 μg g−1 for iron, 0.47–5.05 μg g−1 for manganese, and 1.55–15.12 μg g−1 for zinc in multivitamin tablets. The accuracy of the proposed method was established by a comparison with the conventional wet acid digestion method using a paired t-test, indicating the absence of systematic errors. PMID:22567553

  6. A green analytical method using ultrasound in sample preparation for the flow injection determination of iron, manganese, and zinc in soluble solid samples by flame atomic absorption spectrometry.

    PubMed

    Yebra, M Carmen

    2012-01-01

    A simple and rapid analytical method was developed for the determination of iron, manganese, and zinc in soluble solid samples. The method is based on continuous ultrasonic water dissolution of the sample (5-30 mg) at room temperature followed by flow injection flame atomic absorption spectrometric determination. A good precision of the whole procedure (1.2-4.6%) and a sample throughput of ca. 25 samples h(-1) were obtained. The proposed green analytical method has been successfully applied for the determination of iron, manganese, and zinc in soluble solid food samples (soluble cocoa and soluble coffee) and pharmaceutical preparations (multivitamin tablets). The ranges of concentrations found were 21.4-25.61 μg g(-1) for iron, 5.74-18.30 μg g(-1) for manganese, and 33.27-57.90 μg g(-1) for zinc in soluble solid food samples and 3.75-9.90 μg g(-1) for iron, 0.47-5.05 μg g(-1) for manganese, and 1.55-15.12 μg g(-1) for zinc in multivitamin tablets. The accuracy of the proposed method was established by a comparison with the conventional wet acid digestion method using a paired t-test, indicating the absence of systematic errors. PMID:22567553

  7. Tracing the Milky Way Nuclear Wind with 21cm Atomic Hydrogen Emission

    NASA Astrophysics Data System (ADS)

    Lockman, Felix J.; McClure-Griffiths, N. M.

    2016-08-01

    There is evidence in 21 cm H i emission for voids several kiloparsecs in size centered approximately on the Galactic center, both above and below the Galactic plane. These appear to map the boundaries of the Galactic nuclear wind. An analysis of H i at the tangent points, where the distance to the gas can be estimated with reasonable accuracy, shows a sharp transition at Galactic radii R ≲ 2.4 kpc from the extended neutral gas layer characteristic of much of the Galactic disk, to a thin Gaussian layer with FWHM ˜ 125 pc. An anti-correlation between H i and γ-ray emission at latitudes 10^\\circ ≤slant | b| ≤slant 20^\\circ suggests that the boundary of the extended H i layer marks the walls of the Fermi Bubbles. With H i, we are able to trace the edges of the voids from | z| \\gt 2 {{kpc}} down to z ≈ 0, where they have a radius ˜2 kpc. The extended Hi layer likely results from star formation in the disk, which is limited largely to R ≳ 3 kpc, so the wind may be expanding into an area of relatively little H i. Because the H i kinematics can discriminate between gas in the Galactic center and foreground material, 21 cm H i emission may be the best probe of the extent of the nuclear wind near the Galactic plane.

  8. REVIEWS OF TOPICAL PROBLEMS: Spontaneous and induced emission of a Rydberg atom in a cavity

    NASA Astrophysics Data System (ADS)

    Beterov, I. M.; Lerner, P. B.

    1989-12-01

    Experimental and theoretical studies of Rydberg masers-quantum-electronic devices which produce and employ microwave radiation from highly excited atoms in a cavity-are reviewed. The experimental results are based mainly on studies performed by S. Haroche's group in Paris and H. Walther's group in Munich. In contradistinction to the usual quantum generators the quantum properties of the electromagnetic field itself play an important role in the analysis of the behavioral dynamics of Rydberg masers. The most striking results obtained in this field are the discovery of "quantum revival" and the achievement of maser generation on two-photon transitions and Fok states of the electromagnetic field.

  9. Kinetic Energy Distribution of D(2p) Atoms From Analysis of the D Lyman-a Line Profile

    NASA Technical Reports Server (NTRS)

    Ciocca, Marco; Ajello, Joseph M.; Liu, Xianming; Maki, Justin

    1997-01-01

    The absolute cross sections of the line center (slow atoms) and wings (fast atoms) and total emission line profile were measured from threshold to 400 eV. Analytical model coeffiecients are given for the energy dependence of the measured slow atom cross section.

  10. X-ray emission from a high-atomic-number z-pinch plasma created from compact wire arrays

    SciTech Connect

    Sanford, T.W.L.; Nash, T.J.; Marder, B.M.

    1996-03-01

    Thermal and nonthermal x-ray emission from the implosion of compact tungsten wire arrays, driven by 5 MA from the Saturn accelerator, are measured and compared with LLNL Radiation-Hydro-Code (RHC) and SNL Hydro-Code (HC) numerical models. Multiple implosions, due to sequential compressions and expansions of the plasma, are inferred from the measured multiple x-radiation bursts. Timing of the multiple implosions and the thermal x-ray spectra measured between 1 and 10 keV are consistent with the RHC simulations. The magnitude of the nonthermal x-ray emission measured from 10 to 100 keV ranges from 0.02 to 0.08% of the total energy radiated and is correlated with bright-spot emission along the z-axis, as observed in earlier Gamble-11 single exploding-wire experiments. The similarities of the measured nonthermal spectrum and bright-spot emission with those measured at 0.8 MA on Gamble-II suggest a common production mechanism for this process. A model of electron acceleration across magnetic fields in highly-collisional, high-atomic-number plasmas is developed, which shows the existence of a critical electric field, E{sub c}, below which strong nonthermal electron creation (and the associated nonthermal x rays) do not occur. HC simulations show that significant nonthermal electrons are not expected in this experiment (as observed) because the calculated electric fields are at least one to two orders-of-magnitude below E{sub c}. These negative nonthermal results are confirmed by RHC simulations using a nonthermal model based on a Fokker-Plank analysis. Lastly, the lower production efficiency and the larger, more irregular pinch spots formed in this experiment relative to those measured on Gamble II suggest that implosion geometries are not as efficient as single exploding-wire geometries for warm x-ray production.

  11. Heavy metal adsorptivity of calcium-alginate-modified diethylenetriamine-silica gel and its application to a flow analytical system using flame atomic absorption spectrometry.

    PubMed

    Mori, Masanobu; Suzuki, Toshinobu; Sugita, Tsuyoshi; Nagai, Daisuke; Hirayama, Kazuo; Onozato, Makoto; Itabashi, Hideyuki

    2014-08-20

    This study aimed to evaluate the heavy metal adsorptivity of calcium-alginate-modified diethylenetriamine-silica gel (CaAD) and incorporate this biosorbent into a flow analytical system for heavy metal ions using flame atomic absorption spectrometry (FAAS). The biosorbent was synthesized by electrostatically coating calcium alginate onto diethylenetriamine (dien)-silica gel. Copper ion adsorption tests by a batch method showed that CaAD exhibited a higher adsorption rate compared with other biosorbents despite its low maximum adsorption capacity. Next, CaAD was packed into a 1mL microcolumn, which was connected to a flow analytical system equipped with an FAAS instrument. The flow system quantitatively adsorbed heavy metals and enriched their concentrations. This quantitative adsorption was achieved for pH 3-4 solutions containing 1.0×10(-6) M of heavy metal ions at a flow rate of 5.0 mL min(-1). Furthermore, the metal ions were successfully desorbed from CaAD at low nitric acid concentrations (0.05-0.15 M) than from the polyaminecarboxylic acid chelating resin (Chelex 100). Therefore, CaAD may be considered as a biosorbent that quickly adsorbs and easily desorbs analyte metal ions. In addition, the flow system enhanced the concentrations of heavy metals such as Cu(2+), Zn(2+), and Pb(2+) by 50-fold. This new enrichment system successfully performed the separation and determination of Cu(2+) (5.0×10(-8)M) and Zn(2+) (5.7×10(-8) M) in a river water sample and Pb(2+) (3.8×10(-9) M) in a ground water sample.

  12. Heavy metal adsorptivity of calcium-alginate-modified diethylenetriamine-silica gel and its application to a flow analytical system using flame atomic absorption spectrometry.

    PubMed

    Mori, Masanobu; Suzuki, Toshinobu; Sugita, Tsuyoshi; Nagai, Daisuke; Hirayama, Kazuo; Onozato, Makoto; Itabashi, Hideyuki

    2014-08-20

    This study aimed to evaluate the heavy metal adsorptivity of calcium-alginate-modified diethylenetriamine-silica gel (CaAD) and incorporate this biosorbent into a flow analytical system for heavy metal ions using flame atomic absorption spectrometry (FAAS). The biosorbent was synthesized by electrostatically coating calcium alginate onto diethylenetriamine (dien)-silica gel. Copper ion adsorption tests by a batch method showed that CaAD exhibited a higher adsorption rate compared with other biosorbents despite its low maximum adsorption capacity. Next, CaAD was packed into a 1mL microcolumn, which was connected to a flow analytical system equipped with an FAAS instrument. The flow system quantitatively adsorbed heavy metals and enriched their concentrations. This quantitative adsorption was achieved for pH 3-4 solutions containing 1.0×10(-6) M of heavy metal ions at a flow rate of 5.0 mL min(-1). Furthermore, the metal ions were successfully desorbed from CaAD at low nitric acid concentrations (0.05-0.15 M) than from the polyaminecarboxylic acid chelating resin (Chelex 100). Therefore, CaAD may be considered as a biosorbent that quickly adsorbs and easily desorbs analyte metal ions. In addition, the flow system enhanced the concentrations of heavy metals such as Cu(2+), Zn(2+), and Pb(2+) by 50-fold. This new enrichment system successfully performed the separation and determination of Cu(2+) (5.0×10(-8)M) and Zn(2+) (5.7×10(-8) M) in a river water sample and Pb(2+) (3.8×10(-9) M) in a ground water sample. PMID:25086892

  13. Analytically useful spectra excited in an atmospheric pressure active nitrogen afterglow

    SciTech Connect

    Rice, G.W.; D'Silva, A.P.; Fassel, V.A.

    1984-03-01

    An atmospheric pressure active nitrogen (APAN) discharge has been utilized for producing characteristic molecular emissions from nonmetallic species introduced into the afterglow region of the discharge. The addition of inorganic S-, P-, B-, Cl-, and Br-containing compounds into the afterglow has resulted in the formation of excited S/sub 2/, PN, BO, NCl, and NBr species, respectively. Intense molecular Br/sub 2/ emission and I/sub 2/ emission, as well as atomic I emission, have also been observed. Preliminary analytical utilization of the molecular or atomic emissions observed revealed that the APAN afterglow may serve as a potentially useful detector for the aforementioned elements.

  14. Subnanogram determination of inorganic and organic mercury by helium-microwave induced plasma-atomic emission spectrometry

    SciTech Connect

    Fukushi, K. ); Willie, S.N.; Sturgeon, R.E. )

    1993-02-01

    Inorganic and organic mercury were determined by helium-microwave induced plasma-atomic emission spectrometry following cold vapor generation. Whereas only inorganic mercury was reduced by stannous ion in an acidic medium, both inorganic and organic mercury (total mercury) were reduced by stannous ion in the presence of cupric ion in a basic medium. Organic mercury was determined as the difference between total and inorganic mercury. Detection limits for inorganic and organic mercury were 11 and 10 pg, respectively. The accuracy of the proposed method was verified through the determination of inorganic, total and organic mercury in two marine biological standard reference materials, DORM-1 and TORT-1. 21 refs., 1 fig., 4 tabs.

  15. Study of soft X-ray emission from Z-pinches with a complex atomic composition

    SciTech Connect

    Volkov, G. S.; Zaitsev, V. I.; Grabovski, E. V.; Fedulov, M. V.; Aleksandrov, V. V.; Lakhtyushko, N. I.

    2010-03-15

    Results are presented from experimental studies of Z-pinches produced by implosion of aluminum and tungsten cylindrical wire arrays in the Angara-5-1 facility. The electron temperature T{sub e} and density n{sub e} of the high-temperature pinch plasma have been determined by analyzing line emission from multicharged ions. For the same mass and radius of the array and the same number of wires in it, the intensity of line emission of H- and He-like Al ions from an imploded Al + W wire array containing even a small amount of tungsten (7 wt %) is one order of magnitude lower than that from an Al array. As the W content increases, the total soft X-ray (SXR) yield increases, while the duration of the SXR pulse decreases. For the 30% W content in the array, the power and duration of the SXR pulse are nearly the same as those recorded during the implosion of a W array with the same linear mass and radius and the same number of wires. Results are also presented from experiments with nested wire arrays in which the outer and inner shells were made of Al and W wires, respectively. It is found that, in this case, the effect of tungsten on the line emission of aluminum is much weaker than that in experiments with arrays in which tungsten and aluminum wires were placed in the same shell, even if the mass of the inner (tungsten) shell was larger than that of the outer (aluminum) one. At the same time, the inner W shell plays a significant role in the implosion dynamics of a nested wire array, reducing the duration of the SXR pulse and increasing the SXR power.

  16. Effect of the electronic structure of target atoms on the emission continuum of laser plasma

    SciTech Connect

    Kask, Nikolai E; Michurin, Sergei V; Fedorov, Gennadii M

    2004-06-30

    The low-temperature laser plasma at the surface of metal targets is experimentally investigated. Continuous spectra emitted from a laser plume are found to be similar for targets consisting of the elements of the same subgroup of the Mendeleev periodic table. The similarity manifests itself both in the dependence of the emission intensity on the external pressure and in the structure of absorption bands related to a fine-dispersed phase existing in the peripheral regions of the plume. (interaction of laser radiation with matter. laser plasma)

  17. Dressed projectile charge state dependence of differential electron emission from Ne atom

    NASA Astrophysics Data System (ADS)

    Biswas, S.; Monti, J. M.; Rivarola, R. D.; Tribedi, L. C.

    2015-01-01

    We study the projectile charge state dependence of doubly differential electron emission cross section (DDCS) in ionization of Ne under the impact of dressed and bare oxygen ions. Experimental DDCS results measured at different angles are compared with the calculations based on a CDW-EIS approximation using the GSZ model potential to describe projectile active-electron interaction. This prescription gives an overall very good agreement. In general a deviation from the q2-law was observed in the DDCS. The observations crudely identify the dominance of different projectile electron loss mechanisms at certain electron energy range.

  18. Electron Emission Properties and Surface Atom Behavior of an Impregnated Cathode Coated with Tungsten Thin Film Containing Sc2O3

    NASA Astrophysics Data System (ADS)

    Yamamoto, Shigehiko; Taguchi, Sadanori; Watanabe, Isato; Kawase, Susumu

    1986-07-01

    A new cathode has been developed which shows similar electron emission characteristics as a previously reported Sc2O3 mixed matrix impregnated cathode (Sc2O3 MM Cathode). Contrary to the Sc2O3 MM cathode, the new cathode is resistive to prolonged heating at high temperatures and to ion bombardment. This has been made possible by applying to a standard impregnated cathode a tungsten thin-film containing about 5 weight percent Sc2O3. The electron-emission property is found to be strongly linked to the surface atom composition as well as to the distribution of surface atoms.

  19. [A genetic algorithm approach to qualitative analysis in inductively coupled plasma-atomic emission spectroscopy].

    PubMed

    Peng, Bin; Liu, Ke-ling; Li, Zhi-min; Wang, Yue-song; Huang, Tu-jiang

    2002-06-01

    Genetic algorithm (GA) is used in automatic qualitative analysis by a sequential inductively coupled plasma spectrometer (ICP-AES) and a computer program is developed in this paper. No any standard samples are needed, and spectroscopic interferences can be eliminated. All elements and their concentration ranges of an unknown sample can be reported. The replication rate Pr, crossover rate Pc, and mutation rate of the genetic algorithm were adjusted to be 0.6, 0.4 and 0 respectively. The analytical results of GA are in good agreement with the reference values. It indicates that, combined with the intensity information, the GA can be applied to spectroscopic qualitative analysis and expected to become an effective method in qualitative analysis in ICP-AES after further work. PMID:12938334

  20. Development of a coincidence system for the measurement of X-ray emission atomic parameters

    NASA Astrophysics Data System (ADS)

    Martínez, Filiberto; Miranda, Javier

    2013-07-01

    Preliminary results obtained in experiments carried out with an x-ray spectrometer built at the Instituto de Física for Atomic Physics and environmental sciences studies are presented. The experiments are based on a coincidence method for signals produced by LEGe and Si(Li) detectors. The x-ray fluorescence yields (ωLi) and Coster-Kronig transition probabilities (fij) for elements with 55 ≤ Z ≤ 60 are among the quantities of interest. The method is based on the simultaneous detection of K x-rays with the LEGe detector and the L x-rays with the Si(Li) detector. The primary radiation source is an x-ray tube with Rh anode. The system was tested with the coincidence of the L x-rays from Ce with its K line, demonstrating the feasibility of the experiments.

  1. Infrared light emission from nano hot electron gas created in atomic point contacts

    NASA Astrophysics Data System (ADS)

    Malinowski, T.; Klein, H. R.; Iazykov, M.; Dumas, Ph.

    2016-06-01

    Gold atomic point contacts are prototype systems to evidence ballistic electron transport. The typical dimension of the nanojunction being smaller than the electron-phonon interaction length, even at room temperature, electrons transfer their excess energy to the lattice only far from the contact. At the contact however, favored by huge current densities, electron-electron interactions result in a nano hot electron gas acting as a source of photons. Using a home built Mechanically Controlled Break Junction, it is reported here, for the first time, that this nano hot electron gas also radiates in the infrared range (0.2 eV to 1.2 eV). Moreover, following the description introduced by Tomchuk et al. (Sov. Phys.-Solid State, 8 (1966) 2510), we show that this radiation is compatible with a black-body-like spectrum emitted from an electron gas at temperatures of several thousands of kelvins.

  2. Development of a coincidence system for the measurement of X-ray emission atomic parameters

    SciTech Connect

    Martinez, Filiberto; Miranda, Javier

    2013-07-03

    Preliminary results obtained in experiments carried out with an x-ray spectrometer built at the Instituto de Fisica for Atomic Physics and environmental sciences studies are presented. The experiments are based on a coincidence method for signals produced by LEGe and Si(Li) detectors. The x-ray fluorescence yields ({omega}{sub Li}) and Coster-Kronig transition probabilities (f{sub ij}) for elements with 55 {<=} Z {<=} 60 are among the quantities of interest. The method is based on the simultaneous detection of K x-rays with the LEGe detector and the L x-rays with the Si(Li) detector. The primary radiation source is an x-ray tube with Rh anode. The system was tested with the coincidence of the L x-rays from Ce with its K line, demonstrating the feasibility of the experiments.

  3. Infrared light emission from nano hot electron gas created in atomic point contacts

    NASA Astrophysics Data System (ADS)

    Malinowski, T.; Klein, H. R.; Iazykov, M.; Dumas, Ph.

    2016-06-01

    Gold atomic point contacts are prototype systems to evidence ballistic electron transport. The typical dimension of the nanojunction being smaller than the electron-phonon interaction length, even at room temperature, electrons transfer their excess energy to the lattice only far from the contact. At the contact however, favored by huge current densities, electron-electron interactions result in a nano hot electron gas acting as a source of photons. Using a home built Mechanically Controlled Break Junction, it is reported here, for the first time, that this nano hot electron gas also radiates in the infrared range (0.2 eV to 1.2 eV). Moreover, following the description introduced by Tomchuk et al. (Sov. Phys.-Solid State, 8 (1966) 2510), we show that this radiation is compatible with a black-body–like spectrum emitted from an electron gas at temperatures of several thousands of kelvins.

  4. Wafer-Size and Single-Crystal MoSe2 Atomically Thin Films Grown on GaN Substrate for Light Emission and Harvesting.

    PubMed

    Chen, Zuxin; Liu, Huiqiang; Chen, Xuechen; Chu, Guang; Chu, Sheng; Zhang, Hang

    2016-08-10

    Two-dimensional (2D) atomic-layered semiconductors are important for next-generation electronics and optoelectronics. Here, we designed the growth of an MoSe2 atomic layer on a lattice-matched GaN semiconductor substrate. The results demonstrated that the MoSe2 films were less than three atomic layers thick and were single crystalline of MoSe2 over the entire GaN substrate. The ultrathin MoSe2/GaN heterojunction diode demonstrated ∼850 nm light emission and could also be used in photovoltaic applications. PMID:27409977

  5. Wafer-Size and Single-Crystal MoSe2 Atomically Thin Films Grown on GaN Substrate for Light Emission and Harvesting.

    PubMed

    Chen, Zuxin; Liu, Huiqiang; Chen, Xuechen; Chu, Guang; Chu, Sheng; Zhang, Hang

    2016-08-10

    Two-dimensional (2D) atomic-layered semiconductors are important for next-generation electronics and optoelectronics. Here, we designed the growth of an MoSe2 atomic layer on a lattice-matched GaN semiconductor substrate. The results demonstrated that the MoSe2 films were less than three atomic layers thick and were single crystalline of MoSe2 over the entire GaN substrate. The ultrathin MoSe2/GaN heterojunction diode demonstrated ∼850 nm light emission and could also be used in photovoltaic applications.

  6. Pesticide analysis in herbal infusions by solid-phase microextraction and gas chromatography with atomic emission detection.

    PubMed

    Campillo, Natalia; Peñalver, Rosa; Hernández-Córdoba, Manuel

    2007-02-28

    A direct immersion solid-phase microextraction (SPME) procedure was used in combination with capillary gas chromatography with atomic emission detection (GC-AED) for the determination of 10 pesticides (organochlorines, organophosphorus compounds and pyrethrins) in herbal and tea infusions. Ionic strength, sample dilution and time and temperature of the absorption and desorption stages were some of the parameters investigated in order to select the optimum conditions for SPME with a 100mum PDMS fiber-coating. Element-specific detection and quantification was carried out by monitoring the chlorine (479nm) and bromine (478nm) emission lines, which provided nearly specific chromatograms. Calibration was carried out by using a spiked sample infusion. The detection limits varied between 11.9ngml(-1) for deltamethrin and 0.03ngml(-1) for p,p'-DDE and p,p'-DDD. The recoveries ranged from 73.5% for deltamethrin to 108.3% for p,p'-DDT in a spiked white tea infusion. Two of the eight samples analyzed contained low levels of some the pesticides considered. PMID:19071467

  7. The interaction of 193-nm excimer laser radiation with single-crystal zinc oxide: The generation of atomic Zn line emission at laser fluences below breakdown

    SciTech Connect

    Khan, Enamul H.; Langford, S. C.; Dickinson, J. T.; Boatner, L. A.

    2013-08-28

    The production of gas phase atomic and ionic line spectra accompanying the high laser fluence irradiation of solid surfaces is well known and is most often due to the production and interaction of high densities of atoms, ions, and electrons generated from laser-induced breakdown. The resulting plasma expands and moves rapidly away from the irradiated spot and is accompanied by intense emission of light. This type of “plume” is well studied and is frequently exploited in the technique of chemical analysis known as laser induced breakdown spectroscopy. Here, we describe a similar but weaker emission of light generated in vacuum by the laser irradiation of single crystal ZnO at fluences well below breakdown; this emission consists entirely of optical line emission from excited atomic Zn. We compare the properties of the resulting laser-generated gas-phase light emission (above and below breakdown) and describe a mechanism for the production of the low-fluence optical emission resulting from a fortuitous choice of material and laser wavelength.

  8. Rapid coal analysis. Part II: Slurry atomization DCP emission analysis of NBS coal

    SciTech Connect

    McCurdy, D.L.; Wichman, M.D.; Fry, R.C.

    1985-11-01

    A McCrone Micronising Mills is used to wet grind NBS bituminous coal to a median particle diameter of 5.7 m within 10 min. The finely divided coal slurry is immediately nebulized without sieving into a three-electrode DCP for accurate trace element determinations within 15 min overall lapsed time. Three important parameters contribute to near-quantitative elemental recovery without the use of wet or dry ashing, matrix matching, standard additions, as correction factors. These parameters are: (1) extremely small coal particle size, (2) spray chamber conditions favoring unusually efficient characteristic of the hot DCP. Near-unity response factors are observed for the rapid DCP emission determination of trace metals in finely divided coal slurry. Calibration may therefore be performed simply with aqueous standards. The slurry method gives near quantitative agreement between experimental and certified values for Cr, Cu, Mg, Mn, Ni, and Pb in NBS bituminous coal.

  9. An atomic orbital-based formulation of analytical gradients and nonadiabatic coupling vector elements for the state-averaged complete active space self-consistent field method on graphical processing units

    SciTech Connect

    Snyder, James W.; Hohenstein, Edward G.; Luehr, Nathan; Martínez, Todd J.

    2015-10-21

    We recently presented an algorithm for state-averaged complete active space self-consistent field (SA-CASSCF) orbital optimization that capitalizes on sparsity in the atomic orbital basis set to reduce the scaling of computational effort with respect to molecular size. Here, we extend those algorithms to calculate the analytic gradient and nonadiabatic coupling vectors for SA-CASSCF. Combining the low computational scaling with acceleration from graphical processing units allows us to perform SA-CASSCF geometry optimizations for molecules with more than 1000 atoms. The new approach will make minimal energy conical intersection searches and nonadiabatic dynamics routine for molecular systems with O(10{sup 2}) atoms.

  10. MPTS-silica coated capillary microextraction on line hyphenated with inductively coupled plasma atomic emission spectrometry for the determination of Cu, Hg and Pb in biological samples.

    PubMed

    Zheng, Fei; Hu, Bin

    2007-09-15

    A novel sol-gel 3-mercaptopropyltrimethoxysilane (MPTS) modified silica coating was developed for capillary microextraction (CME) of trace Cu, Hg and Pb prior to their on line determination by inductively coupled plasma-atomic emission spectrometry (ICP-AES). This organic-inorganic hybrid coating was in situ created on the inner walls of fused silica capillary using a sol solution containing TMOS (tetramethoxysilane) as a precursor, MPTS as a co-precursor, ethanol as the solvent and hydrochloric acid as a catalyst. The structure of the capillary coating was characterized by FT-IR spectroscopy, Raman spectroscopy, SEM and TEM. The factors affecting on the capillary microextraction of analytes such as pH, sample flow rate and volume, elution solution and interfering ions had been investigated, and the optimized experimental parameters were obtained. Under the optimized conditions, the absorption capacity of MPTS-silica coated capillary was found to be 1.17, 1.96 and 1.19mugm(-1) for Cu, Hg and Pb, and the limits of detection were as low as 0.17 0.22 and 0.52ngmL(-1), respectively. With a sampling frequency of 12h(-1), the relative standard deviations (R.S.D.s) were 4.2, 2.6 and 3.8% (C=4ngmL(-1), n=7, sample volume=1mL) for Cu, Hg and Pb, respectively. The proposed method had been successfully applied to the determination of Cu, Hg and Pb in human urine, human serum and preserved egg. To validate the proposed method, certified reference materials of BCR151 milk powder, GBW07601 (GSH-1) human hair, GSBZ 50016-90 and GSB 07-1183-2000 water samples were analyzed and the determined values were in a good agreement with the certified values.

  11. Tungsten coil atomic emission spectrometry combined with dispersive liquid-liquid microextraction: A synergistic association for chromium determination in water samples.

    PubMed

    Vidal, Lorena; Silva, Sidnei G; Canals, Antonio; Nóbrega, Joaquim A

    2016-02-01

    A novel and environment friendly analytical method is reported for total chromium determination and chromium speciation in water samples, whereby tungsten coil atomic emission spectrometry (WCAES) is combined with in situ ionic liquid formation dispersive liquid-liquid microextraction (in situ IL-DLLME). A two stage multivariate optimization approach has been developed employing a Plackett-Burman design for screening and selection of the significant factor involved in the in situ IL-DLLME procedure, which was later optimized by means of a circumscribed central composite design. The optimum conditions were complexant concentration: 0.5% (or 0.1%); complexant type: DDTC; IL anion: PF6(-); [Hmim][Cl] IL amount: 60 mg; ionic strength: 0% NaCl; pH: 5 (or 2); centrifugation time: 10 min; and centrifugation speed: 1000 rpm. Under the optimized experimental conditions the method was evaluated and proper linearity was obtained with a correlation coefficient of 0.991 (5 calibration standards). Limits of detection and quantification for both chromium species were 3 and 10 µg L(-1), respectively. This is a 233-fold improvement when compared with chromium determination by WCAES without using preconcentration. The repeatability of the proposed method was evaluated at two different spiking levels (10 and 50 µg L(-1)) obtaining coefficients of variation of 11.4% and 3.6% (n=3), respectively. A certified reference material (SRM-1643e NIST) was analyzed in order to determine the accuracy of the method for total chromium determination and 112.3% and 2.5 µg L(-1) were the recovery (trueness) and standard deviation values, respectively. Tap, bottled mineral and natural mineral water samples were analyzed at 60 µg L(-1) spiking level of total Cr content at two Cr(VI)/Cr(III) ratios, and relative recovery values ranged between 88% and 112% showing that the matrix has a negligible effect. To our knowledge, this is the first time that combines in situ IL-DLLME and WCAES.

  12. High speed analysis of agricultural samples using inductively coupled plasma-atomic emission spectroscopy

    NASA Astrophysics Data System (ADS)

    Isaac, R. A.; Johnson, W. C.

    The determination of potassium, phosphorus, calcium, magnesium, zinc and manganese in soil extracts are reported at an analysis rate of 200 samples h -1. A 4 cm 3volume of soil is extracted with a 20 ml solution of 0.025 N H 2SO 4-0.05 N HCl (Mehlich I). The filtered solution is then placed on a Technicon Sampler IV, which is interfaced to an 1CP emission spectrometer. This extract is analyzed for all the nutrients above. In addition to soil extracts, the ICP is used for mineral analyses of feed samples at a sample rate of 120 samples h -1. Several "American Association of Feed Control Officials" check feed samples have been analyzed and the results will be discussed comparing the ICP results with other laboratories participating in the program. The preparation of feed samples involves ashing a 1 g sample at 500°C for 4 h. The ashed sample was then taken up in hot HCl and diluted to 250 ml. Analyses are also performed by ICP on water, heavy metals in sewage sludge, and on other materials. The ICP technique has increased the efficiency of our laboratory to the extent that one technician can do the same work that formerly required four technicians.

  13. Atomic Emission, Absorption and Fluorescence in the Laser-induced Plasma

    SciTech Connect

    Winefordner, J. D.

    2009-01-22

    The main result of our efforts is the development and successful application of the theoretical model of laser induced plasma (LIP) that allows a back-calculation of the composition of the plasma (and the condensed phase) based on the observable plasma spectrum. The model has an immediate experimental input in the form of LIP spectra and a few other experimentally determined parameters. The model is also sufficiently simple and, therefore, practical. It is conveniently interfaced in a graphical user-friendly form for using by students and any laboratory personnel with only minimal training. In our view, the model opens up the possibility for absolute analysis, i.e. the analysis which requires no standards and tedious calibration. The other parts of this proposal (including plasma diagnostics) were somewhat subordinate to this main goal. Plasma diagnostics provided the model with the necessary experimental input and led to better understanding of plasma processes. Another fruitful direction we pursued was the use of the correlation analysis for material identification and plasma diagnostics. Through a number of computer simulations we achieved a clear understanding of how, where and why this approach works being applied to emission spectra from a laser plasma. This understanding will certainly improve the quality of forensic and industrial analyses where fast and reliable material identification and sorting are required.

  14. Measuring atomic emission from beacons for long-distance chemical signaling.

    PubMed

    LaFratta, Christopher N; Pelse, Ian; Falla, Jose Luis; Liu, Yi; Palacios, Manuel A; Manesse, Mael; Whitesides, George M; Walt, David R

    2013-10-01

    In an effort to exploit chemistry for information science, we have constructed a system to send a message powered by a combustion reaction. Our system uses the thermal excitation of alkali metals to transmit an encoded signal over long distances. A message is transmitted by burning a methanol-soaked cotton string embedded with combinations of high, low, or zero levels of potassium, rubidium, and/or cesium ions. By measuring the intensities at the characteristic emission wavelengths of each metal in the near-infrared, 19 unique signals can be distinguished. We have built a custom telescope to detect these signals from 1 km away for nearly 10 min. The signal is isotropic, is self-powered, and has a low background. A potential application of this platform is for search and rescue signaling where another layer of information can be transmitted, in addition to the location of the beacon. This work, which seeks to encode and transmit information using chemistry instead of electronics, is part of the new field of "infochemistry".

  15. Determination of Vanadium, Tin and Mercury in Atmospheric Particulate Matter and Cement Dust Samples by Direct Current Plasma Atomic Emission Spectrometry.

    ERIC Educational Resources Information Center

    Hindy, Kamal T.; And Others

    1992-01-01

    An atmospheric pollution study applies direct current plasma atomic emission spectrometry (DCP-AES) to samples of total suspended particulate matter collected in two industrial areas and one residential area, and cement dust collected near major cement factories. These samples were analyzed for vanadium, tin, and mercury. The results indicate the…

  16. A Preliminary Investigation into the Mitigation of Plug-in Hybrid Electric Vehicle Tailpipe Emissions Through Supervisory Control Methods Part 1: Analytical Development of Energy Management Strategies

    SciTech Connect

    Smith, David E; Lohse-Busch, Henning; Irick, David Kim

    2010-01-01

    Plug-in hybrid electric vehicle (PHEV) technologies have the potential for considerable petroleum consumption reductions, possibly at the expense of increased tailpipe emissions due to multiple 'cold' start events and improper use of the engine for PHEV specific operation. PHEVs operate predominantly as electric vehicles (EVs) with intermittent assist from the engine during high power demands. As a consequence, the engine can be subjected to multiple cold start events. These cold start events may have a significant impact on the tailpipe emissions due to degraded catalyst performance and starting the engine under less than ideal conditions. On current hybrid electric vehicles (HEVs), the first cold start of the engine dictates whether or not the vehicle will pass federal emissions tests. PHEV operation compounds this problem due to infrequent, multiple engine cold starts. The research is broken down into two (2) distinct phases, involving both analytical and experimental areas. Phase I of the research, addressed in this document, focuses on the design of a vehicle supervisory control system for a pre-transmission parallel PHEV powertrain architecture. A suitable control system architecture is created and implemented into a standard vehicle modeling tool (in this case, the Powertrain Systems Analysis Toolkit). Energy management strategies are evaluated and implemented in a virtual environment for preliminary assessment of petroleum displacement benefits and rudimentary drivability issues. Engine cold start events are aggressively addressed in the development of this control system, which leads to enhanced pre-warming and energy-based engine warming algorithms that provide substantial reductions in tailpipe emissions over the baseline supervisory control strategy. The flexibility of the PHEV powertrain offers the potential for decreased emissions during any engine starting event through powertrain 'torque shaping' algorithms. The analytical work presented here is

  17. Evaluation of an improved atomic data basis for carbon in UEDGE emission modeling for L-mode plasmas in DIII-D

    NASA Astrophysics Data System (ADS)

    Muñoz Burgos, J. M.; Leonard, A. W.; Loch, S. D.; Ballance, C. P.

    2013-07-01

    New scaled carbon atomic electron-impact excitation data is utilized to evaluate comparisons between experimental measurements and fluid emission modeling of detached plasmas at DIII-D. The C I and C II modeled emission lines for 909.8 and 514.7 nm were overestimated by a factor of 10-20 than observed experimentally for the inner leg, while the outer leg was within a factor of 2. Due to higher modeled emissions, a previous study using the UEDGE code predicted that a higher amount of carbon was required to achieve a detached outboard divertor plasma in L-mode at DIII-D. The line emission predicted by using the new scaled carbon data yields closer results when compared against experiment. We also compare modeling and measurements of Dα emission from neutral deuterium against predictions from newly calculated R-Matrix with pseudostates data available at the ADAS database.

  18. Flame-in-gas-shield and miniature diffusion flame hydride atomizers for atomic fluorescence spectrometry: optimization and comparison

    NASA Astrophysics Data System (ADS)

    Marschner, Karel; Musil, Stanislav; Dědina, Jiří

    2015-07-01

    A detailed optimization of relevant experimental parameters of two hydride atomizers for atomic fluorescence spectrometry: flame-in-gas-shield atomizer with a two-channel shielding unit and a standard atomizer for atomic fluorescence spectrometry, miniature diffusion flame, was performed. Arsine, generated by the reaction with NaBH4 in a flow injection arrangement, was chosen as the model hydride. Analytical characteristics of both the atomizers (sensitivity, noise, limits of detection) were compared. Under optimum conditions sensitivity obtained with flame-in-gas-shield atomizer was approximately twice higher than with miniature diffusion flame. The additional advantage of flame-in-gas-shield atomizer is significantly lower flame emission resulting in a better signal to noise ratio. The resulting arsenic limits of detection for miniature diffusion flame and flame-in-gas-shield atomizer were 3.8 ng l- 1 and 1.0 ng l- 1, respectively.

  19. Determination of selected elements in whole coal and in coal ash from the eight argonne premium coal samples by atomic absorption spectrometry, atomic emission spectrometry, and ion-selective electrode

    USGS Publications Warehouse

    Doughten, M.W.; Gillison, J.R.

    1990-01-01

    Methods for the determination of 24 elements in whole coal and coal ash by inductively coupled argon plasma-atomic emission spectrometry, flame, graphite furnace, and cold vapor atomic absorption spectrometry, and by ion-selective electrode are described. Coal ashes were analyzed in triplicate to determine the precision of the methods. Results of the analyses of NBS Standard Reference Materials 1633, 1633a, 1632a, and 1635 are reported. Accuracy of the methods is determined by comparison of the analysis of standard reference materials to their certified values as well as other values in the literature.

  20. Optical emission spectroscopy of metal-halide lamps: Radially resolved atomic state distribution functions of Dy and Hg

    NASA Astrophysics Data System (ADS)

    Nimalasuriya, T.; Flikweert, A. J.; Stoffels, W. W.; Haverlag, M.; van der Mullen, J. J. A. M.; Pupat, N. B. M.

    2006-03-01

    Absolute line intensity measurements are performed on a metal-halide lamp. Several transitions of atomic and ionic Dy and atomic Hg are measured at different radial positions from which we obtain absolute atomic and ionic Dy intensity profiles. From these profiles we construct the radially resolved atomic state distribution function (ASDF) of the atomic and ionic Dy and the atomic Hg. From these ASDFs several quantities are determined as functions of radial position, such as the (excitation) temperature, the ion ratio Hg+/Dy+, the electron density, the ground state, and the total density of Dy atoms and ions. Moreover, these ASDFs give us insight about the departure from equilibrium. The measurements show a hollow density profile for the atoms and the ionization of atoms in the center. In the outer parts of the lamp molecules dominate.

  1. Optical emission spectroscopy of metal-halide lamps: Radially resolved atomic state distribution functions of Dy and Hg

    SciTech Connect

    Nimalasuriya, T.; Flikweert, A.J.; Stoffels, W.W.; Haverlag, M.; Mullen, J.J.A.M. van der; Pupat, N.B.M.

    2006-03-01

    Absolute line intensity measurements are performed on a metal-halide lamp. Several transitions of atomic and ionic Dy and atomic Hg are measured at different radial positions from which we obtain absolute atomic and ionic Dy intensity profiles. From these profiles we construct the radially resolved atomic state distribution function (ASDF) of the atomic and ionic Dy and the atomic Hg. From these ASDFs several quantities are determined as functions of radial position, such as the (excitation) temperature, the ion ratio Hg{sup +}/Dy{sup +}, the electron density, the ground state, and the total density of Dy atoms and ions. Moreover, these ASDFs give us insight about the departure from equilibrium. The measurements show a hollow density profile for the atoms and the ionization of atoms in the center. In the outer parts of the lamp molecules dominate.

  2. Improvement of sensitivity of electrolyte cathode discharge atomic emission spectrometry (ELCAD-AES) for mercury using acetic acid medium.

    PubMed

    Shekhar, R

    2012-05-15

    A method has been developed to improve the sensitivity of the electrolyte cathode discharge atomic emission spectrometry (ELCAD-AES) for mercury determination. Effects of various low molecular weight organic solvents at different volume percentages as well as at different acid molarities on the mercury signal were investigated using ELCAD-AES. The addition of few percent of organic solvent, acetic acid produced significant enhancement in mercury signal. Acetic acid of 5% (v/v) with the 0.2M acidity has been found to give 500% enhancement for mercury signal in flow injection mode. Under the optimized parameters the repeatability, expressed as the percentage relative standard deviation of spectral peak area for mercury with 5% acetic acid was found to be 10% for acid blank solution and 5% for 20 ng/mL mercury standard based on multiple measurements with a multiple sample loading in flow injection mode. Limit of detection of this method was determined to be 2 ng/mL for inorganic mercury. The proposed method has been validated by determining mercury in certified reference materials, Tuna fish (IAEA-350) and Aquatic plant (BCR-060). Accuracy of the method for the mercury determination in the reference materials has been found to be between 3.5% and 5.9%. This study enhances the utility of ELCAD-AES for various types of biological and environmental materials to quantify total mercury at very low levels. PMID:22483872

  3. Improvement of sensitivity of electrolyte cathode discharge atomic emission spectrometry (ELCAD-AES) for mercury using acetic acid medium.

    PubMed

    Shekhar, R

    2012-05-15

    A method has been developed to improve the sensitivity of the electrolyte cathode discharge atomic emission spectrometry (ELCAD-AES) for mercury determination. Effects of various low molecular weight organic solvents at different volume percentages as well as at different acid molarities on the mercury signal were investigated using ELCAD-AES. The addition of few percent of organic solvent, acetic acid produced significant enhancement in mercury signal. Acetic acid of 5% (v/v) with the 0.2M acidity has been found to give 500% enhancement for mercury signal in flow injection mode. Under the optimized parameters the repeatability, expressed as the percentage relative standard deviation of spectral peak area for mercury with 5% acetic acid was found to be 10% for acid blank solution and 5% for 20 ng/mL mercury standard based on multiple measurements with a multiple sample loading in flow injection mode. Limit of detection of this method was determined to be 2 ng/mL for inorganic mercury. The proposed method has been validated by determining mercury in certified reference materials, Tuna fish (IAEA-350) and Aquatic plant (BCR-060). Accuracy of the method for the mercury determination in the reference materials has been found to be between 3.5% and 5.9%. This study enhances the utility of ELCAD-AES for various types of biological and environmental materials to quantify total mercury at very low levels.

  4. [Characterization of dinosaur fossils and their surrounding rocks by atomic emission spectrometry and X-ray powder diffractometry].

    PubMed

    Yang, Qun; Wang, Yi-lin; Li, Chao-zhen; Yuan, Bo

    2005-02-01

    More dinosaur fossils have been found in the Laochangqing valley, Lufeng county than anywhere else in the world, and the dinosaur fossils found here cover the longest time span (including the early and middle Jurassic ages). This excavation offers an ideal experimental base for prehistoric biology studies. This paper presents an elementary analysis of the components and structure of the dinosaur fossils in three different geologic-layers and their surrounding rocks in the above mentioned area. Atomic emission spectrum shows that the fossils are rich in the contents of calcium (>5%) and phosphor, but low in the content of silicon (3%-8%), while the surrounding rocks are high in the content of silicon (>10%). Furthermore, XRD results show that the major compound of the fossils is CaCO3 (66%), followed by SiO2 (17%); while that of the surrounding rocks is SiO2 (>80%), followed by CaCO3 (<12%). The most important difference between the fossils and the surrounding rocks is, according to the experiment, that phosphate has been identified in the former but not in the latter. This is a characteristic that can be used to distinguish the dinosaur fossils from other rocks. This paper provides valuable data for further zoological studies on the living conditions and evolution of the dinosaurs in the Laochangqing valley, Lufeng county.

  5. TH-C-BRD-01: Analytical Computation of Prompt Gamma Ray Emission and Detection for Proton Range Verification

    SciTech Connect

    Sterpin, E; Vynckier, S; Janssens, G; Smeets, J; Prieels, D

    2014-06-15

    Purpose: A prompt gamma (PG) slit camera prototype demonstrated that on-line range monitoring within 1–2 mm could be performed by comparing expected and measured PG detection profiles. Monte Carlo (MC) can simulate the expected PG profile but this would result in prohibitive computation time for a complete pencil beam treatment plan. We implemented a much faster method that is based on analytical processing of pre-computed MC data. Methods: The formation of the PG detection signal can be separated into: 1) production of PGs and 2) detection by the camera detectors after PG transport in geometry. For proton energies from 40 to 230 MeV, PG productions in depth were pre-computed by MC (PENH) for 12C, 14N, 16O, 31P and 40Ca. The PG production was then modeled analytically by adding the PG production for each element according to local proton energy and tissue composition.PG transport in the patient/camera geometries and the detector response were modeled by convolving the PG production profile with a transfer function. The latter is interpolated from a database of transfer functions fitted to pre-computed MC data (PENELOPE). The database was generated for a photon source in a cylindrical phantom with various radiuses and a camera placed at various positions.As a benchmark, the analytical model was compared to PENH for a water phantom, a phantom with different slabs (adipose, muscle, lung) and a thoracic CT. Results: Good agreement (within 5%) was observed between the analytical model and PENH for the PG production. Similar accuracy for detecting range shifts was also observed. Speed of around 250 ms per profile was achieved (single CPU) using a non-optimized MatLab implementation. Conclusion: We devised a fast analytical model for generating PG detection profiles. In the test cases considered in this study, similar accuracy than MC was achieved for detecting range shifts. This research is supported by IBA.

  6. X-RAY NONLINEAR OPTICAL PROCESSES IN ATOMS USING A SELF-AMPLIFIED SPONTANEOUS EMISSION FREE-ELECTRON LASER

    SciTech Connect

    Rohringer, N

    2008-08-08

    X-ray free electron lasers (xFEL) will open new avenues to the virtually unexplored territory of non-linear interactions of x rays with matter. Initially xFELs will be based on the principle of self-amplified spontaneous emission (SASE). Each SASE pulse consists of a number of coherent intensity spikes of random amplitude, i.e. the process is chaotic and pulses are irreproducible. The coherence time of SASE xFELs will be a few femtoseconds for a photon energy near 1 keV. The importance of coherence properties of light in non-linear optical processes was theoretically discovered in the early 1960s. In this contribution we will illustrate the impact of field chaoticity on x-ray non-linear optical processes on neon for photon energies around 1 keV and intensities up to 10{sup 18} W/cm{sup 2}. Resonant and non-resonant processes are discussed. The first process to be addressed is the formation of a double-core hole in neon by photoionization with x rays above 1.25 keV energy. In contrast to the long-wavelength regime, non-linear optical processes in the x-ray regime are characterized in general by sequential single-photon single-electron interactions. Despite this fact, the sequential absorption of multiple x-ray photons depends on the statistical properties of the radiation field. Treating the x rays generated by a SASE FEL as fully chaotic, a quantum-mechanical analysis of inner-shell two-photon absorption is performed. By solving a system of time-dependent rate equations, we demonstrate that double-core hole formation in neon via x-ray two-photon absorption is enhanced by chaotic photon statistics. At an intensity of 10{sup 16} W/cm{sup 2}, the statistical enhancement is about 30%, much smaller than typical values in the optical regime. The second part of this presentation discusses the resonant Auger effect of atomic neon at the 1s-3p transition (at 867.1 eV). For low X-ray intensity, the excitation process 1s {yields} 3p in Neon can be treated perturbatively. The

  7. Prediction of CO Cameron band and atomic oxygen visible emissions in comets C/2013 A1 (Siding Spring) and 67P/Churyumov-Gerasimenko

    NASA Astrophysics Data System (ADS)

    Raghuram, S.; Bhardwaj, A.

    2014-04-01

    The forbidden emissions of cometary species have special importance in the cometary spectra. The excited species which produce these forbidden emissions can not be populated by direct solar radiation excitation. These metastable species are produced mainly from dissociative excitation and ion-electron recombination reactions. Thus the observed emissions have been used as tracers of parent cometary species. The CO (a3 -X1) is a forbidden transition which produces Cameron band emission in the ultraviolet region during dissociative excitation of CObearing neutrals and the dissociative recombination of CO-ionic species in the cometary coma. Similarly, the forbidden transitions of metastable atomic oxygen 1S-3P (green, 5577 Å), and 1D-3P (red-doublet, 6300 and 6364 Å) produce line emissions in the visible region. These emissions have been used to probe H2O and CO2 abundances in the comets. We have developed a coupled chemistry-emission model to study various production and loss mechanisms of these excited metastable states. The model is applied to comet C/2013 A1 (Siding Spring) which will have a close fly-by of Mars during mid October, 2014, when Indian Mars orbiter Mission and NASA's Maven, would be orbiting the planet. The model is also applied on ESA's Rosetta mission target comet 67P/Churyumov-Gerasimenko which will be useful for different observations over various heliocentric distances. The predicted intensities and quantitative analysis of these emissions can be a theoretical support for various space and ground-based observations.

  8. Modification and control of coherence effects in the spontaneous emission spectrum of a three-level atom at weak field regime

    NASA Astrophysics Data System (ADS)

    Dutta, Bibhas Kumar; Panchadhyayee, Pradipta

    2016-09-01

    It has been shown that coherence effects have a marked influence in the spontaneous emission spectrum of a three-level Λ -type atom driven by weak coherent and incoherent fields. Phase dependent evolution of interference effects leading to spectral narrowing, generation of spectral hole and dark line are exhibited in the present scheme when the atom does not interact with the incoherent fields. The basic mechanism underlying this scheme seems to be appropriate for a phaseonium. Apart from phase-coherence introduced in the system the phenomenon of line narrowing, in the presence of weak incoherent pumping, can be achieved in a different way as a consequence of two competitive resonant effects: sharp non-Lorentzian and symmetric Fano-like-resonance contributions to the line shape. In both the situations, the evolution of narrow structures in the line shape can be achieved even when the emission is influenced by the dephasing of Raman coherence.

  9. Spectral evolution of energetic neutral atom emissions at the heliospheric poles as measured by IBEX during its first three years

    SciTech Connect

    Dayeh, M. A.; Allegrini, F.; Desai, M. I.; Ebert, R. W.; Fuselier, S. A.; Livadiotis, G.; McComas, D. J.; Schwadron, N. A.; DeMajistre, R.; Janzen, P.; Reisenfeld, D.; Siewert, M.

    2014-12-10

    The Interstellar Boundary Explorer (IBEX) mission continues to measure energetic neutral atom (ENA) emissions produced by charge exchange between solar wind (SW) protons and interstellar neutrals at the edge of our heliosphere. Using the first 3 yr of IBEX-Hi ENA measurements (2009-2011), we examined the spectral evolution of ∼0.5-6 keV ENAs at the polar regions (above 60°). We found the following: (1) pixels with a characteristic 'ankle' spectra (lower spectral index at higher energies) increase by ∼5% in 2010 and ∼10% in 2011 compared to 2009. (2) The averaged spectral index in 2011 is smaller than that of 2009. (3) The slope of the ENA spectrum above ∼1.7 keV is more variable than the slope below ∼1.7 keV. The lower spectral index at higher energies of the spectrum does not appear to be caused by an increase of the ENA production at these energies, but rather from a consistent decrease at lower energies. (4) The decrease in polar ENA fluxes does not correlate significantly with the averaged SW dynamic pressure, back-traced in time to 1 AU along the flow streamlines (originating between 10° and 30° for slow SW, and 60° and 80° for fast SW), assuming these are the respective conditions of ENA progenitors back in time. These results provide insights into the complexity of relating the slow and fast SW contributions to polar ENAs and shed light on how the solar output and the resulting change in the global heliospheric structure possibly affect the heliosheath (HS) populations.

  10. The use of ion chromatography-dc plasma atomic emission spectrometry for the speciation of trace metals

    SciTech Connect

    Urasa, I.T.

    1991-09-20

    The original objects of this research program were: to interface d.c. plasma atomic emission spectrometer with an ion chromatograph; to characterize and optimize the combined systems for application in the speciation of metals in aqueous solutions; to use this system in the study of the solution chemistry of various metals; and to find ways in which the measurement sensitivity of the method can be enhanced, thereby allowing the detection of metal species at low ppb concentration levels. This approach has been used to study the chemistry of and speciate several elements in solution including: arsenic, chromium, iron, manganese, nickel phosphorus, platinum, selenium, and vanadium. During the course of this research, we have found that the solution chemistry of the elements studied and the speciation data obtained can vary considerably depending on the solution, and the chromatographic conditions employed. The speciation of chromium, iron, and vanadium was found to be highly influenced by the acidity of the sample. The element selective nature of the d.c. plasma detector allows these changes to be monitored, thereby providing quantitative information on the new moieties formed. New approaches are being developed including the use of chelating ligands as preconcentration agents for purposes of reducing further the detection limits of the elements of interest and to improve the overall element speciation scheme. New thrusts are being directed towards the employment of post-column derivatization method coupled with colorimetric measurements to detect and quantify metal species eluting from the chromatographic column. The influence of sample acidity on these investigations will be carefully evaluated. These new thrusts are described in the accompanying Project Renewal Proposal.

  11. X-ray emission spectroscopy applied to glycine adsorbed on Cu(110): An atom and symmetry projected view

    SciTech Connect

    Hasselstroem, J.; Karis, O.; Weinelt, M.

    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.

  12. Spectral Evolution of Energetic Neutral Atom Emissions at the Heliospheric Poles as Measured by IBEX during its First Three Years

    NASA Astrophysics Data System (ADS)

    Dayeh, M. A.; Allegrini, F.; DeMajistre, R.; Desai, M. I.; Ebert, R. W.; Fuselier, S. A.; Janzen, P.; Livadiotis, G.; McComas, D. J.; Reisenfeld, D.; Schwadron, N. A.; Siewert, M.

    2014-12-01

    The Interstellar Boundary Explorer (IBEX) mission continues to measure energetic neutral atom (ENA) emissions produced by charge exchange between solar wind (SW) protons and interstellar neutrals at the edge of our heliosphere. Using the first 3 yr of IBEX-Hi ENA measurements (2009-2011), we examined the spectral evolution of ~0.5-6 keV ENAs at the polar regions (above 60°). We found the following: (1) pixels with a characteristic "ankle" spectra (lower spectral index at higher energies) increase by ~5% in 2010 and ~10% in 2011 compared to 2009. (2) The averaged spectral index in 2011 is smaller than that of 2009. (3) The slope of the ENA spectrum above ~1.7 keV is more variable than the slope below ~1.7 keV. The lower spectral index at higher energies of the spectrum does not appear to be caused by an increase of the ENA production at these energies, but rather from a consistent decrease at lower energies. (4) The decrease in polar ENA fluxes does not correlate significantly with the averaged SW dynamic pressure, back-traced in time to 1 AU along the flow streamlines (originating between 10° and 30° for slow SW, and 60° and 80° for fast SW), assuming these are the respective conditions of ENA progenitors back in time. These results provide insights into the complexity of relating the slow and fast SW contributions to polar ENAs and shed light on how the solar output and the resulting change in the global heliospheric structure possibly affect the heliosheath (HS) populations.

  13. Methods of atomic oxygen and ozone retrieval from observations of the O2 dayglow emissions in the MLT region

    NASA Astrophysics Data System (ADS)

    Yankovsky, Valentine; Martyshenko, Kseniia; Manuilova, Rada

    2015-04-01

    The problem of creating the new methods of remote sensing of altitude profile of the [O(3P)] and [O3] in the daytime is actual for the mesosphere and lower thermosphere range. Currently there is no reliable method for remote sensing of altitude profile of the [O(3P)], but atomic oxygen is a key component in the mechanism of the atmosphere cooling by quenching of vibrationally excited CO2 molecules and also one of basic quencher of excited components in MLT region. The airglow emission in 1.27 µm IR Atm(0 - 0) band from [O2(a1Δg, v=0)] has been used as a proxy for [O3] in MLT for over a decade. However, lifetime of O2(a1Δg, v=0) is more than 1 hour, therefore this method is not suitable for detecting of relatively rapid [O3] variations which occur due to the variability of the solar spectrum in the UV range (120 - 320 nm) and other space factors. The aim of this study is revealing of proxies for retrievals of [O(3P)] and [O3]. In the framework of developed model of electronic vibrational kinetics of excited products of O3 and O2 photolysis in MLT of the Earth (model YM-2011) [1] we consider the photolysis of O2 in the Schumann-Runge continuum and Lyaman-A H atom and of O3 in Hartley band and for excited products of photolysis ( O2(a1Δg, v=0 - 5), O2(b1Σ+g, v=0, 1, 2) and excited oxygen atom O(1D)) we took into account more than 60 aeronomical reactions of photoexcitation and deexcitation by energy transfer between the excited levels and of quenching of the levels in collisions with O(3P) O2, N2, O(3P), O3, CO2. We tested 5 excited components, namely, O2(b1Σ+g, v=0, 1, 2), O2(a1Δg, v=0 - 5) and O(1D) as the O(3P) and O3 proxies. The total system of kinetic equations for 10 components has been solved and altitude profiles of concentrations of O(1D), O2(b1Σ+g, v=0, 1, 2), and O2(a1Δg, v=0 - 5) have been calculated. To compare characteristics of assumed proxies we used sensitivity analysis of the proxy concentrations altitude profiles to variations of [O3] and

  14. Development of a partial least-squares calibration model for simultaneous determination of elements by inductively coupled plasma-atomic emission spectrometry.

    PubMed

    Chaloosi, Marzieh; Asadollahi, Seyed Azadeh; Khanchi, Ali Reza; FirozZare, Mahmoud; Mahani, Mohamad Khayatzadeh

    2009-01-01

    A partial least-squares (PLS) calibration model was developed for simultaneous multicomponent elemental analysis with inductively coupled plasma-atomic emission spectrometry (ICP-AES) in the presence of spectral interference. The best calibration model was obtained using a PLS2 algorithm. Validation was performed with an artificial test set. Multivariate calibration models were constructed using 2 series of synthetic mixtures (Zn, Cu, Fe, and U, V). Accuracy of the method was evaluated with unknown synthetic and real samples. PMID:19382589

  15. Electron emission spectra of thermal collisions of He metastable atoms with Au(111) and Pt(111) surfaces: Evidence for Penning ionization

    SciTech Connect

    Masuda, S.; Sasaki, K.; Sogo, M.; Aoki, M.; Morikawa, Y.

    2009-10-15

    Electron emission spectra obtained by thermal collisions of He*(2{sup 1}S and 2{sup 3}S) atoms with Au(111) and Pt(111) surfaces were measured to clarify the electronically excited atom-metal interactions. It has been recognized that the metastable atoms de-excite on ordinary noble- and transition-metal surfaces via resonance ionization (RI) followed by Auger neutralization (AN) without no indication of Penning ionization (PI). Our data show that this traditional criterion partially breaks down in the He*-Au(111) collision system. The local electronic states near the surface were examined by first-principles calculations using density functional theory. It reveals that the itinerant sp states are significantly spilled out toward the vacuum compared to the localized 5d states, and their asymptotic features play a crucial role in determining the branching ratio between PI and RI+AN.

  16. Tungsten coil atomic emission spectrometry combined with dispersive liquid-liquid microextraction: A synergistic association for chromium determination in water samples.

    PubMed

    Vidal, Lorena; Silva, Sidnei G; Canals, Antonio; Nóbrega, Joaquim A

    2016-02-01

    A novel and environment friendly analytical method is reported for total chromium determination and chromium speciation in water samples, whereby tungsten coil atomic emission spectrometry (WCAES) is combined with in situ ionic liquid formation dispersive liquid-liquid microextraction (in situ IL-DLLME). A two stage multivariate optimization approach has been developed employing a Plackett-Burman design for screening and selection of the significant factor involved in the in situ IL-DLLME procedure, which was later optimized by means of a circumscribed central composite design. The optimum conditions were complexant concentration: 0.5% (or 0.1%); complexant type: DDTC; IL anion: PF6(-); [Hmim][Cl] IL amount: 60 mg; ionic strength: 0% NaCl; pH: 5 (or 2); centrifugation time: 10 min; and centrifugation speed: 1000 rpm. Under the optimized experimental conditions the method was evaluated and proper linearity was obtained with a correlation coefficient of 0.991 (5 calibration standards). Limits of detection and quantification for both chromium species were 3 and 10 µg L(-1), respectively. This is a 233-fold improvement when compared with chromium determination by WCAES without using preconcentration. The repeatability of the proposed method was evaluated at two different spiking levels (10 and 50 µg L(-1)) obtaining coefficients of variation of 11.4% and 3.6% (n=3), respectively. A certified reference material (SRM-1643e NIST) was analyzed in order to determine the accuracy of the method for total chromium determination and 112.3% and 2.5 µg L(-1) were the recovery (trueness) and standard deviation values, respectively. Tap, bottled mineral and natural mineral water samples were analyzed at 60 µg L(-1) spiking level of total Cr content at two Cr(VI)/Cr(III) ratios, and relative recovery values ranged between 88% and 112% showing that the matrix has a negligible effect. To our knowledge, this is the first time that combines in situ IL-DLLME and WCAES. PMID:26653490

  17. The glow discharge as an atomization and ionization device

    SciTech Connect

    Harrison, W.W.

    1990-01-01

    All of our projects involve the glow discharge source as our basic research focus. Our primary effort is glow discharge mass spectrometry, but we frequently use complementary procedures such as atomic absorption and atomic emission in the glow discharge to obtain useful information about plasma processes. Our overall goal is to gain a better understanding of the glow discharge and to bring it to bear on real analytical problems.

  18. Effect of entanglement on the decay dynamics of a pair of H(2p) atoms due to spontaneous emission

    SciTech Connect

    Tanabe, Takehiko; Odagiri, Takeshi; Nakano, Motoyoshi; Kumagai, Yoshiaki; Kitajima, Masashi; Kouchi, Noriyuki; Suzuki, Isao H.

    2010-10-15

    We have measured the coincidence time spectra of two Lyman-{alpha} photons emitted by a pair of H(2p) atoms in the photodissociation of H{sub 2} at the incident photon energy of 33.66 eV and at the hydrogen gas pressures of 0.40 and 0.02 Pa. The decay time constant at 0.02 Pa is approximately half the lifetime of a single H(2p) atom, 1.60 ns, while the decay time constant at 0.40 Pa is in agreement with the lifetime of a single H(2p) atom. It turns out that the decay faster than the lifetime of a single H(2p) atom originates from the entanglement in the pair of H(2p) atoms. We have demonstrated an effect of entanglement on atomic decay.

  19. Studying the R-branch and the Q-branch emission spectral lines of diatomic molecules using improved analytical formula

    NASA Astrophysics Data System (ADS)

    Jiang, Yonghong; Sun, Weiguo; Zhang, Yi; Fu, Jia; Fan, Qunchao; Li, Huidong; Feng, Hao

    2016-06-01

    The difference converging method (DCM) used to predict the R-branch and the Q-branch high-lying rotational lines for diatomic systems is improved in this study. The key analytical formulae of the DCM method are modified by adding a higher order spectral term Hυ, and adding a physical converging criterion to improve the accuracy of predictions. Applications of the improved DCM method to the R-branch of the TiF molecule and the Q-branch of the 193IrN molecule show that the accuracy of the R-branch and the Q-branch rotational lines is about one order of magnitude better than the results obtained using the previous formulae, which demonstrate the necessity of the added small term Hυ and the physical converging criterion. The DCM results are also shown to be better than the extrapolated rotational lines using the least-squares method.

  20. Analytic model of ion emission from the focus of an intense relativistic electron beam on a target

    SciTech Connect

    Caporaso, G J; Chen, Y J

    1998-08-23

    Advanced radiographic systems for stockpile stewardship require very small x-ray sources to achieve the required resolution. Focusing multi-kiloampere beams to diameters on the order of 1 mm onto a Bremsstrahlung target leads to the generation of axial electric fields on the order of several MV/cm which act to extract ions out of the surface plasma and accelerate them upstream into the beam. These backstreaming ions act as a distributed electrostatic lens which can perturb the focus of the electron beam in a time varying manner during the pulse. An analytic model of the ion extraction is presented for a particular target geometry along with scaling laws for the perturbation of the focal spot.

  1. Enhanced free exciton and direct band-edge emissions at room temperature in ultrathin ZnO films grown on Si nanopillars by atomic layer deposition.

    PubMed

    Chang, Yuan-Ming; Shieh, Jiann; Chu, Pei-Yuan; Lee, Hsin-Yi; Lin, Chih-Ming; Juang, Jenh-Yih

    2011-11-01

    Room-temperature ultraviolet (UV) luminescence was investigated for the atomic layer deposited ZnO films grown on silicon nanopillars (Si-NPs) fabricated by self-masking dry etching in hydrogen-containing plasma. For films deposited at 200 °C, an intensive UV emission corresponding to free-exciton recombination (~3.31 eV) was observed with a nearly complete suppression of the defect-associated broad visible range emission peak. On the other hand, for ZnO films grown at 25 °C, albeit the appearance of the defect-associated visible emission, the UV emission peak was observed to shift by ~60 meV to near the direct band edge (3.37 eV) recombination emission. The high-resolution transmission electron microscopy (HRTEM) showed that the ZnO films obtained at 25 °C were consisting of ZnO nanocrystals with a mean radius of 2 nm embedded in a largely amorphous matrix. Because the Bohr radius of free-exictons in bulk ZnO is ~2.3 nm, the size confinement effect may have occurred and resulted in the observed direct band edge electron-hole recombination. Additionally, the results also demonstrate order of magnitude enhancement in emission efficiency for the ZnO/Si-NP structure, as compared to that of ZnO directly deposited on Si substrate under the same conditions.

  2. Analytical calculation of the light-collection efficiency of an optical emission spectrometer with the effective solid-angle method.

    PubMed

    Kang, Minwook; Hahn, Jae W

    2016-05-20

    A method is proposed for calculating the optical emission spectrometer (OES) light-collection efficiency using the effective solid angle from an arbitrary point source. Based on the point source-OES relative positioning, the effective solid angle is derived for four cases: (1) on axis and on the object plane; (2) on axis and outside the object plane; (3) off axis and on the object plane; and (4) off axis and outside the object plane. The results were in good agreement with those obtained through Monte Carlo ray tracing. After calculating the OES geometrical collection efficiency with respect to the object plane distance in three different-sized cylindrical volume sources, we suggest a simple strategy to increase this efficiency in plasma process monitoring. PMID:27411114

  3. QED Theory of Radiation Emission and Absorption Lines for Atoms and Ions in a Strong Laser Field

    SciTech Connect

    Glushkov, A. V.

    2008-10-22

    The results of numerical calculating the multi-photon resonance shift and width for transition 6S-6F in the atom of Cs (wavelength 1059nm) in a laser pulse of the Gaussian and soliton-like shapes are presented. QED theory of radiation atomic lines is used.

  4. Single-photon superradiance and radiation trapping by atomic shells

    NASA Astrophysics Data System (ADS)

    Svidzinsky, Anatoly A.; Li, Fu; Li, Hongyuan; Zhang, Xiwen; Ooi, C. H. Raymond; Scully, Marlan O.

    2016-04-01

    The collective nature of light emission by atomic ensembles yields fascinating effects such as superradiance and radiation trapping even at the single-photon level. Light emission is influenced by virtual transitions and the collective Lamb shift which yields peculiar features in temporal evolution of the atomic system. We study how two-dimensional atomic structures collectively emit a single photon. Namely, we consider spherical, cylindrical, and spheroidal shells with two-level atoms continuously distributed on the shell surface and find exact analytical solutions for eigenstates of such systems and their collective decay rates and frequency shifts. We identify states which undergo superradiant decay and states which are trapped and investigate how size and shape of the shell affects collective light emission. Our findings could be useful for quantum information storage and the design of optical switches.

  5. An analytical study of nitrogen oxides and carbon monoxide emissions in hydrocarbon combustion with added nitrogen - Preliminary results

    NASA Technical Reports Server (NTRS)

    Bittker, D. A.

    1980-01-01

    The influence of ground-based gas turbine combustor operating conditions and fuel-bound nitrogen (FBN) found in coal-derived liquid fuels on the formation of nitrogen oxides and carbon monoxide is investigated. Analytical predictions of NOx and CO concentrations are obtained for a two-stage, adiabatic, perfectly-stirred reactor operating on a propane-air mixture, with primary equivalence ratios from 0.5 to 1.7, secondary equivalence ratios of 0.5 or 0.7, primary stage residence times from 12 to 20 msec, secondary stage residence times of 1, 2 and 3 msec and fuel nitrogen contents of 0.5, 1.0 and 2.0 wt %. Minimum nitrogen oxide but maximum carbon monoxide formation is obtained at primary zone equivalence ratios between 1.4 and 1.5, with percentage conversion of FBN to NOx decreasing with increased fuel nitrogen content. Additional secondary dilution is observed to reduce final pollutant concentrations, with NOx concentration independent of secondary residence time and CO decreasing with secondary residence time; primary zone residence time is not observed to affect final NOx and CO concentrations significantly. Finally, comparison of computed results with experimental values shows a good semiquantitative agreement.

  6. Laboratory-scale evaluation of various sampling and analytical methods for determining mercury emissions from coal-fired power plants

    SciTech Connect

    Agbede, R.O.; Bochan, A.J.; Clements, J.L.

    1995-11-01

    Comparative bench-scale mercury sampling method tests were performed at the Advanced Technology Systems, Inc. (ATS) laboratories for EPA Method 101A, EPA Method 29 and the Ontario Hydro Method. Both blank and impinger spiking experiments were performed. The experimental results show that the ambient level of mercury in the ATS laboratory is at or below the detection limit (10 ng Hg) as measured by a cold vapor atomic absorption spectrophotometer (CVAAS) which was used to analyze the mercury samples. From the mercury spike studies, the following observations and findings were made. (a) The recovery of mercury spikes using EPA Method 101A was 104%. (b) The Ontario Hydro Method retains about 90% of mercury spikes in the first absorbing solution but has a total spike retention of 106%. As a result, the test data shows possible migration of spiked mercury from the first impinger solution (KCI) to the permanganate impingers. (c) For the EPA Method 29 solutions, when only the peroxide impingers were spiked, mercury recoveries were 65.6% for the peroxide impingers, 0.1% for the knockout impinger and 32.8% for the permanganate impingers with an average total mercury recovery of 98.4%. At press time, data was still being obtained for both the peroxide and permanganate impinger solution spikes. This and other data will be available at the presentation.

  7. Spectra, Emission Yields, Cross Sections, and Kinetic Energy Distributions of Hydrogen Atoms from H2 X 1Eg+-d 3IIu Excitation by Electron Impact

    NASA Astrophysics Data System (ADS)

    Liu, Xianming; Shemansky, Donald E.; Yoshii, Jean; Johnson, Paul V.; Malone, Charles P.; Ajello, Joseph M.

    2016-02-01

    Electron-impact excitation of H2 triplet states plays an important role in the heating of outer planet upper thermospheres. The {d}3{{{\\Pi }}}u state is the third ungerade triplet state, and the {d}3{{{\\Pi }}}u-a{}3{{{Σ }}}g+ emission is the largest cascade channel for the a{}3{{{Σ }}}g+ state. Accurate energies of the d{}3{{{\\Pi }}}u-(v, J) levels are calculated from an ab initio potential energy curve. Radiative lifetimes of the {d}3{{{\\Pi }}}u(v, J) levels are obtained by an accurate evaluation of the {d}3{{{\\Pi }}}u-a{}3{{{Σ }}}g+ transition probabilities. The emission yields are determined from experimental lifetimes and calculated radiative lifetimes and are further verified by comparing experimental and synthetic {d}3{{{\\Pi }}}u-a{}3{{{Σ }}}g+ spectra at 20 eV impact energy. Spectral analysis revealed that multipolar components beyond the dipolar term are required to model the {X}1{{{Σ }}}g+-{d}3{{{\\Pi }}}u excitation, and significant cascade excitation occurs at the {d}3{{{\\Pi }}}u(v = 0,1) levels. Kinetic energy (Ek) distributions of H atoms produced via predissociation of the {d}3{{{\\Pi }}}u state and the {d}3{{{\\Pi }}}u-a{}3{{{Σ }}}g+-b{}3{{{Σ }}}u+ cascade dissociative emission are obtained. Predissociation of the {d}3{{{\\Pi }}}u state produces H atoms with an average Ek of 2.3 ± 0.4 eV/atom, while the Ek distribution of the {d}3{{{\\Pi }}}u-a{}3{{{Σ }}}g+-b{}3{{{Σ }}}u+ channel is similar to that of the {X}1{{{Σ }}}g+-a{}3{{{Σ }}}g+-b{}3{{{Σ }}}u+ channel and produces H(1s) atoms with an average Ek of 1.15 ± 0.05 eV/atom. On average, each H2 excited to the {d}3{{{\\Pi }}}u state in an H2-dominated atmosphere deposits 3.3 ± 0.4 eV into the atmosphere, while each H2 directly excited to the a{}3{{{Σ }}}g+ state gives 2.2-2.3 eV to the atmosphere. The spectral distribution of the calculated a{}3{{{Σ }}}g+ -b{}3{{{Σ }}}u+ continuum emission due to the {X}1{{{Σ }}}g+-{d}3{{{\\Pi }}}u excitation is significantly different from

  8. HERSCHEL KEY PROGRAM, ''DUST, ICE, AND GAS IN TIME'' (DIGIT): THE ORIGIN OF MOLECULAR AND ATOMIC EMISSION IN LOW-MASS PROTOSTARS IN TAURUS

    SciTech Connect

    Lee, Jeong-Eun; Lee, Seokho; Lee, Jinhee; Evans II, Neal J.; Green, Joel D.

    2014-10-01

    Six low-mass embedded sources (L1489, L1551-IRS5, TMR1, TMC1-A, L1527, and TMC1) in Taurus have been observed with Herschel-PACS to cover the full spectrum from 50 to 210 μm as part of the Herschel key program, ''Dust, Ice, and Gas In Time''. The relatively low intensity of the interstellar radiation field surrounding Taurus minimizes contamination of the [C II] emission associated with the sources by diffuse emission from the cloud surface, allowing study of the [C II] emission from the source. In several sources, the [C II] emission is distributed along the outflow, as is the [O I] emission. The atomic line luminosities correlate well with each other, as do the molecular lines, but the atomic and molecular lines correlate poorly. The relative contribution of CO to the total gas cooling is constant at ∼30%, while the cooling fraction by H{sub 2}O varies from source to source, suggesting different shock properties resulting in different photodissociation levels of H{sub 2}O. The gas with a power-law temperature distribution with a moderately high density can reproduce the observed CO fluxes, indicative of CO close to LTE. However, H{sub 2}O is mostly subthermally excited. L1551-IRS5 is the most luminous source (Ł{sub bol} = 24.5 L {sub ☉}) and the [O I] 63.1 μm line accounts for more than 70% of its FIR line luminosity, suggesting complete photodissociation of H{sub 2}O by a J shock. In L1551-IRS5, the central velocity shifts of the [O I] line, which exceed the wavelength calibration uncertainty (∼70 km s{sup –1}) of PACS, are consistent with the known redshifted and blueshifted outflow direction.

  9. Herschel Key Program, "Dust, Ice, and Gas In Time" (DIGIT): The Origin of Molecular and Atomic Emission in Low-mass Protostars in Taurus

    NASA Astrophysics Data System (ADS)

    Lee, Jeong-Eun; Lee, Jinhee; Lee, Seokho; Evans, Neal J., II; Green, Joel D.

    2014-10-01

    Six low-mass embedded sources (L1489, L1551-IRS5, TMR1, TMC1-A, L1527, and TMC1) in Taurus have been observed with Herschel-PACS to cover the full spectrum from 50 to 210 μm as part of the Herschel key program, "Dust, Ice, and Gas In Time." The relatively low intensity of the interstellar radiation field surrounding Taurus minimizes contamination of the [C II] emission associated with the sources by diffuse emission from the cloud surface, allowing study of the [C II] emission from the source. In several sources, the [C II] emission is distributed along the outflow, as is the [O I] emission. The atomic line luminosities correlate well with each other, as do the molecular lines, but the atomic and molecular lines correlate poorly. The relative contribution of CO to the total gas cooling is constant at ~30%, while the cooling fraction by H2O varies from source to source, suggesting different shock properties resulting in different photodissociation levels of H2O. The gas with a power-law temperature distribution with a moderately high density can reproduce the observed CO fluxes, indicative of CO close to LTE. However, H2O is mostly subthermally excited. L1551-IRS5 is the most luminous source (Łbol = 24.5 L ⊙) and the [O I] 63.1 μm line accounts for more than 70% of its FIR line luminosity, suggesting complete photodissociation of H2O by a J shock. In L1551-IRS5, the central velocity shifts of the [O I] line, which exceed the wavelength calibration uncertainty (~70 km s-1) of PACS, are consistent with the known redshifted and blueshifted outflow direction.

  10. Number series of atoms, interatomic bonds and interface bonds defining zinc-blende nanocrystals as function of size, shape and surface orientation: Analytic tools to interpret solid state spectroscopy data

    NASA Astrophysics Data System (ADS)

    König, Dirk

    2016-08-01

    Semiconductor nanocrystals (NCs) experience stress and charge transfer by embedding materials or ligands and impurity atoms. In return, the environment of NCs experiences a NC stress response which may lead to matrix deformation and propagated strain. Up to now, there is no universal gauge to evaluate the stress impact on NCs and their response as a function of NC size dNC. I deduce geometrical number series as analytical tools to obtain the number of NC atoms NNC(dNC[i]), bonds between NC atoms Nbnd(dNC[i]) and interface bonds NIF(dNC[i]) for seven high symmetry zinc-blende (zb) NCs with low-index faceting: {001} cubes, {111} octahedra, {110} dodecahedra, {001}-{111} pyramids, {111} tetrahedra, {111}-{001} quatrodecahedra and {001}-{111} quadrodecahedra. The fundamental insights into NC structures revealed here allow for major advancements in data interpretation and understanding of zb- and diamond-lattice based nanomaterials. The analytical number series can serve as a standard procedure for stress evaluation in solid state spectroscopy due to their deterministic nature, easy use and general applicability over a wide range of spectroscopy methods as well as NC sizes, forms and materials.

  11. Non-local-thermodynamical-equilibrium effects in the x-ray emission of radiatively heated materials of different atomic numbers

    NASA Astrophysics Data System (ADS)

    Földes, I. B.; Eidmann, K.; Veres, G.; Bakos, J. S.; Witte, K.

    2001-07-01

    X-ray self-emission of radiatively heated materials with different values of Z has been investigated. Thin foils were uniformly heated by a 120-eV Hohlraum radiation of 400-ps duration in order to study the self-emission of a homogeneous, optically thin material. The x-ray emission spectra were followed for more than 2 ns. The spectrally integrated emission shows not only a strong Z dependence, but different temporal behaviors for different values of Z. The lower is the value of Z of the x-ray heated matter, the longer is the duration of self-emission. Theoretical comparison with a hydrocode and FLY post-processing shows a non-local-thermal equilibrium behavior caused by direct photoionization due to the thermal pumping radiation, which has a higher brightness temperature than the matter temperature of the heated material.

  12. Quantitative Determination of Density of Ground State Atomic Oxygen from Both TALIF and Emission Spectroscopy in Hot Air Plasma Generated by Microwave Resonant Cavity

    NASA Astrophysics Data System (ADS)

    Marchal, F.; Yousfi, M.; Merbahi, N.; Wattieaux, G.; Piquemal, A.

    2016-03-01

    Two experimental techniques have been used to quantify the atomic oxygen density in the case of hot air plasma generated by a microwave (MW) resonant cavity. The latter operates at a frequency of 2.45 GHz inside a cell of gas conditioning at a pressure of 600 mbar, an injected air flow of 12 L/min and an input MW power of 1 kW. The first technique is based on the standard two photon absorption laser induced fluorescence (TALIF) using xenon for calibration but applied for the first time in the present post discharge hot air plasma column having a temperature of about 4500 K near the axis of the nozzle. The second diagnostic technique is an actinometry method based on optical emission spectroscopy (OES). In this case, we compared the spectra intensities of a specific atomic oxygen line (844 nm) and the closest wavelength xenon line (823 nm). The two lines need to be collected under absolutely the same spectroscopic parameters. The xenon emission is due to the addition of a small proportion of xenon (1% Xe) of this chemically inert gas inside the air while a further small quantity of H2 (2%) is also added in the mixture in order to collect OH(A-X) and NH(A-X) spectra without noise. The latter molecular spectra are required to estimate gas and excitation temperatures. Optical emission spectroscopy measurements, at for instance the position z=12 mm on the axis plasma column that leads to a gas measured temperature equal to 3500 K, an excitation temperature of about 9500 K and an atomic oxygen density 2.09×1017±0.2×1017 cm-3. This is in very good agreement with the TALIF measurement, which is equal to 2.0×1017 cm-3.

  13. STEM imaging of 47-pm-separated atomic columns by a spherical aberration-corrected electron microscope with a 300-kV cold field emission gun.

    PubMed

    Sawada, Hidetaka; Tanishiro, Yasumasa; Ohashi, Nobuhiro; Tomita, Takeshi; Hosokawa, Fumio; Kaneyama, Toshikatsu; Kondo, Yukihito; Takayanagi, Kunio

    2009-12-01

    A spherical aberration-corrected electron microscope has been developed recently, which is equipped with a 300-kV cold field emission gun and an objective lens of a small chromatic aberration coefficient. A dumbbell image of 47 pm spacing, corresponding to a pair of atomic columns of germanium aligned along the [114] direction, is resolved in high-angle annular dark field (HAADF) scanning transmission electron microscopy (STEM) with a 0.4-eV energy spread of the electron beam. The observed image was compared with a simulated image obtained by dynamical calculation.

  14. Determination of trace amounts of molybdenum in plant tissue by solvent extraction-atomic-absorption and direct-current plasma emission spectrometry.

    PubMed

    Lajunen, L H; Kubin, A

    1986-03-01

    Methods are presented for determination of molybdenum in plant tissue by flame and graphite-furnace atomic-absorption spectrometry and direct-current argon-plasma emission spectrometry. The samples are digested in HNO(3)-H(2)SO(4)-HC1O(4) mixture, and Mo is separated and concentrated by chelation and extraction. Three organic solvents (methyl isobutyl ketone, di-isobutyl ketone and isoamyl alcohol) and two ligands (8-hydroxyquinoline and toluene-3,4-dithiol) were studied. The procedure were tested on pine needle and birch leaf samples. PMID:18964076

  15. Measurement of the helium 23S metastable atom density by observation of the change in the 23S-23P emission line shape due to radiation reabsorption

    NASA Astrophysics Data System (ADS)

    Shikama, T.; Ogane, S.; Iida, Y.; Hasuo, M.

    2016-01-01

    In helium discharge plasmas, the relative emission intensities of the fine-structure transitions belonging to the HeI 23S-23P transition can be affected by radiation reabsorption. Since the magnitude of the reabsorption depends on the density and temperature of the 23S metastable atoms, their density can be determined by measuring the 23S-23P emission line shape using a high wavelength-resolution spectrometer. In this study, the applicable conditions of the method in terms of the opacity and line broadening are revealed, and possible causes of errors in the measurement, i.e. spatial distributions of the density and temperature and the effects of external magnetic and electric fields, are investigated. The effect of reabsorption under an external magnetic field is experimentally confirmed using a glow discharge plasma installed in a superconducting magnet.

  16. Retrieval algorithm for densities of mesospheric and lower thermospheric metal atom and ion species from satellite-borne limb emission signals

    NASA Astrophysics Data System (ADS)

    Langowski, M.; Sinnhuber, M.; Aikin, A. C.; von Savigny, C.; Burrows, J. P.

    2014-01-01

    Meteoroids bombard Earth's atmosphere during its orbit around the Sun, depositing a highly varying and significant amount of matter into the thermosphere and mesosphere. The strength of the material source needs to be characterized and its impact on atmospheric chemistry assessed. In this study an algorithm for the retrieval of metal atom and ion number densities for a two-dimensional (latitude, altitude) grid is described and explained. Dayglow emission spectra of the mesosphere and lower thermosphere are used, which are obtained by passive satellite remote sensing with the SCIAMACHY (SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY) instrument on board Envisat. The limb scans cover the tangent altitude range from 50 to 150 km. Metal atoms and ions are strong emitters in this region and form sharply peaked layers with a FWHM (full width at half maximum) of several 10 km in the mesosphere and lower thermosphere measuring peak altitudes between 90 to 110 km. The emission signal is first separated from the background signal, arising from Rayleigh and Raman scattering of solar radiation by air molecules. A forward radiative transfer model calculating the slant column density (SCD) from a given vertical distribution was developed. This nonlinear model is inverted in an iterative procedure to yield the vertical profiles for the emitting species. Several constraints are applied to the solution for numerical stability reasons and to get physically reasonable solutions. The algorithm is applied to SCIAMACHY limb-emission observations for the retrieval of Mg and Mg+ using emission signatures at 285.2 and 279.6/280.4 nm, respectively. Results are presented for these three lines as well as error estimations and sensitivity tests on different constraint strength and different separation approaches for the background signal.

  17. Collection of trace evidence of explosive residues from the skin in a death due to a disguised letter bomb. The synergy between confocal laser scanning microscope and inductively coupled plasma atomic emission spectrometer analyses.

    PubMed

    Turillazzi, Emanuela; Monaci, Fabrizio; Neri, Margherita; Pomara, Cristoforo; Riezzo, Irene; Baroni, Davide; Fineschi, Vittorio

    2010-04-15

    In most deaths caused by explosive, the victim's body becomes a depot for fragments of explosive materials, so contributing to the collection of trace evidence which may provide clues about the specific type of device used with explosion. Improvised explosive devices are used which contain "homemade" explosives rather than high explosives because of the relative ease with which such components can be procured. Many methods such as chromatography-mass spectrometry, scanning electron microscopy, stereomicroscopy, capillary electrophoresis are available for use in the identification of explosive residues on objects and bomb fragments. Identification and reconstruction of the distribution of explosive residues on the decedent's body may give additional hints in assessing the position of the victim in relation to the device. Traditionally these residues are retrieved by swabbing the body and clothing during the early phase, at autopsy. Gas chromatography-mass spectrometry and other analytical methods may be used to analyze the material swabbed from the victim body. The histological examination of explosive residues on skin samples collected during the autopsy may reveal significant details. The information about type, quantity and particularly about anatomical distribution of explosive residues obtained utilizing confocal laser scanning microscope (CLSM) together with inductively coupled plasma atomic emission spectrometer (ICP-AES), may provide very significant evidence in the clarification and reconstruction of the explosive-related events. PMID:20047806

  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.

    PubMed

    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).

  19. Collection of trace evidence of explosive residues from the skin in a death due to a disguised letter bomb. The synergy between confocal laser scanning microscope and inductively coupled plasma atomic emission spectrometer analyses.

    PubMed

    Turillazzi, Emanuela; Monaci, Fabrizio; Neri, Margherita; Pomara, Cristoforo; Riezzo, Irene; Baroni, Davide; Fineschi, Vittorio

    2010-04-15

    In most deaths caused by explosive, the victim's body becomes a depot for fragments of explosive materials, so contributing to the collection of trace evidence which may provide clues about the specific type of device used with explosion. Improvised explosive devices are used which contain "homemade" explosives rather than high explosives because of the relative ease with which such components can be procured. Many methods such as chromatography-mass spectrometry, scanning electron microscopy, stereomicroscopy, capillary electrophoresis are available for use in the identification of explosive residues on objects and bomb fragments. Identification and reconstruction of the distribution of explosive residues on the decedent's body may give additional hints in assessing the position of the victim in relation to the device. Traditionally these residues are retrieved by swabbing the body and clothing during the early phase, at autopsy. Gas chromatography-mass spectrometry and other analytical methods may be used to analyze the material swabbed from the victim body. The histological examination of explosive residues on skin samples collected during the autopsy may reveal significant details. The information about type, quantity and particularly about anatomical distribution of explosive residues obtained utilizing confocal laser scanning microscope (CLSM) together with inductively coupled plasma atomic emission spectrometer (ICP-AES), may provide very significant evidence in the clarification and reconstruction of the explosive-related events.

  20. 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.

    PubMed

    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). PMID:26838401

  1. Nonequilibrium dynamics of bosonic atoms in optical lattices: Decoherence of many-body states due to spontaneous emission

    NASA Astrophysics Data System (ADS)

    Pichler, H.; Daley, A. J.; Zoller, P.

    2010-12-01

    We analyze in detail the heating of bosonic atoms in an optical lattice due to incoherent scattering of light from the lasers forming the lattice. Because atoms scattered into higher bands do not thermalize on the time scale of typical experiments, this process cannot be described by the total energy increase in the system alone (which is determined by single-particle effects). The heating instead involves an important interplay between the atomic physics of the heating process and the many-body physics of the state. We characterize the effects on many-body states for various system parameters, where we observe important differences in the heating for strongly and weakly interacting regimes, as well as a strong dependence on the sign of the laser detuning from the excited atomic state. We compute heating rates and changes to characteristic correlation functions based on both perturbation-theory calculations and a time-dependent calculation of the dissipative many-body dynamics. The latter is made possible for one-dimensional systems by combining time-dependent density-matrix-renormalization-group methods with quantum trajectory techniques.

  2. Coherently controlled emissions |4P3/2,1/2> ↔ |4S1/2> from a femtosecond Λ-type excitation scheme in potassium atom

    NASA Astrophysics Data System (ADS)

    Pentaris, D.; Damianos, D.; Papademetriou, G.; Lyras, A.; Steponkevičius, K.; Vaičaitis, V.; Efthimiopoulos, T.

    2016-07-01

    The combined excitation of high density potassium (K) vapour by 100 fs pump-coupling pulses is experimentally studied. The intense pump pulse excites the two-photon ? transition and internally generated emissions are initiated along the atomic paths: ? (path-1) and, ? (path-2). The temporally delayed coupling pulse coherently drives the ? transitions, in a Λ-type excitation scheme. The competing axial and conical emission components of the well-resolved ? transitions (D2 and D1 lines of K) are substantially enhanced and controlled, for appropriate detunings and pump-coupling temporal delays. The coherence relaxation time (CRT) of the two-photon excited ? state is determined by exploiting the temporal delay in the pulse sequence. The effect of the pulse delay and the fs pulse bandwidth on the system dynamics is discussed as well as the role of dephasing collisions between K and buffer gas atoms. The proposed scheme can be employed in radiative multi-level systems, for the direct estimation of coherence relaxation rates of various states.

  3. Native defects affecting the Li atom distribution tune the optical emission of ZnO:Li epitaxial thin film

    SciTech Connect

    Sahu, R.; Dileep, K.; Loukya, B.; Datta, R.

    2014-02-03

    It is found that the oxygen vacancy (V{sub O}) defect concentration affecting the separation between individual species in Li{sub Zn}-Li{sub i} complex influences the optical emission property of Li{sub 0.06}Zn{sub 0.94}O epitaxial thin film grown by pulsed laser deposition. The film grown under low oxygen partial pressure (n-type conductivity)/higher partial pressure (resistive-type) has broad emission at ∼2.99 eV/∼2.1 eV and a narrower emission at 3.63 eV/3.56 eV, respectively. First principle based mBJLDA electronic structure calculation suggests that the emission at 2.99 eV is due to the Li{sub Zn}-Li{sub i} pair complex and the emission at 2.1 eV is when the component species are away from each other.

  4. Some aspects of pulsed laser deposited nanocrystalline LaB(6) film: atomic force microscopy, constant force current imaging and field emission investigations.

    PubMed

    Late, Dattatray J; Date, Kalyani S; More, Mahendra A; Misra, Pankaj; Singh, B N; Kukreja, Lalit M; Dharmadhikari, C V; Joag, Dilip S

    2008-07-01

    Nanocrystalline lanthanum hexaboride (LaB(6)) films have been deposited on molybdenum foil by the pulsed laser deposition (PLD) technique. The as-deposited films were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The XRD pattern shows the cubic crystallinity of the LaB(6) film. The AFM studies reveal that the conical shaped LaB(6) nanostructures have height 60 nm, base 800 nm, and a typical radius of curvature ∼20 nm. A comparison of force and in situ current imaging AFM studies reveals that current contrast does not originate from the surface topography of the LaB(6) film. Field emission studies have been performed in the planar diode configuration. A current density of 4.4 × 10(-2) A cm(-2) is drawn from the actual emitting area. The Fowler-Nordheim plot is found to be linear, in accordance with the quantum mechanical tunneling phenomenon. The field enhancement factor is estimated to be 3585, indicating that the field emission is from LaB(6) nanocrystallites present on the emitter surface, as confirmed by the AFM. The emission current-time plots show current stability to the extent of 5% fluctuation about the average current over a period of 3 h.

  5. Uncertainties in Atomic Data and Their Propagation Through Spectral Models. I.

    NASA Technical Reports Server (NTRS)

    Bautista, M. A.; Fivet, V.; Quinet, P.; Dunn, J.; Gull, T. R.; Kallman, T. R.; Mendoza, C.

    2013-01-01

    We present a method for computing uncertainties in spectral models, i.e., level populations, line emissivities, and emission line ratios, based upon the propagation of uncertainties originating from atomic data.We provide analytic expressions, in the form of linear sets of algebraic equations, for the coupled uncertainties among all levels. These equations can be solved efficiently for any set of physical conditions and uncertainties in the atomic data. We illustrate our method applied to spectral models of Oiii and Fe ii and discuss the impact of the uncertainties on atomic systems under different physical conditions. As to intrinsic uncertainties in theoretical atomic data, we propose that these uncertainties can be estimated from the dispersion in the results from various independent calculations. This technique provides excellent results for the uncertainties in A-values of forbidden transitions in [Fe ii]. Key words: atomic data - atomic processes - line: formation - methods: data analysis - molecular data - molecular processes - techniques: spectroscopic

  6. Experimental and analytical study of a high gain self amplified spontaneous emission free electron laser operating in a large spectral bandwidth regime

    NASA Astrophysics Data System (ADS)

    Andonian, Gerard Cosmos

    The drive to create and measure ultra-short pulses in the x-ray regime advances the ongoing development of free electron lasers (FEL). Several proposed schemes, to shorten the pulse length of the radiation, involve driving the FEL with a chirped (linear longitudinal phase space correlation) electron beam in the self amplified spontaneous emission (SASE) mode. This dissertation examines the experiments conducted under such conditions, canvassing analytical and numerical studies of beam dynamics and radiation properties, experimental observations, and descriptions of the development of novel diagnostics. The VISA (Visible-Infrared SASE Amplifier) program has achieved saturation at 840 nm within a 4 m long undulator. A novel bunch compression mechanism during transport was discovered and ultimately responsible for the high peak current required to drive the FEL. Start-to-end simulations, detailing the dynamics from electron beam inception at the photocathode to the FEL radiation properties at the undulator, were successfully benchmarked to observable data. The VISA II experiment is an extension of this SASE FEL operating under different experimental conditions. Driving the SASE FEL with a chirped electron beam requires maintaining the chirp throughout transport by the use of sextupole magnets to correct for second-order compression effects. The emitted radiation is frequency chirped, diagnosed via a modified frequency resolved optical gating (FROG) technique. Specific numerical simulations and diagnostic developments are presented. A set of measurements, without sextupole corrections, displays anomalous features, namely large spectral bandwidth of the radiation at stable and sustained high gain lasing. The bandwidth has an rms value of 21 nm (12% full width), previously unobserved in a FEL. In addition, the far-field angular distribution yields a hollow mode structure, similar to earlier results yet more pronounced in angle. Start-to-end simulations reproduced the

  7. Direct versus indirect band gap emission and exciton-exciton annihilation in atomically thin molybdenum ditelluride (MoTe2)

    NASA Astrophysics Data System (ADS)

    Froehlicher, Guillaume; Lorchat, Etienne; Berciaud, Stéphane

    2016-08-01

    We probe the room temperature photoluminescence of N -layer molybdenum ditelluride (MoTe2) in the continuous wave (cw) regime. The photoluminescence quantum yield of monolayer MoTe2 is three times larger than in bilayer MoTe2 and 40 times greater than in the bulk limit. Mono- and bilayer MoTe2 display almost symmetric emission lines at 1.10 and 1.07 eV, respectively, which predominantly arise from direct radiative recombination of the A exciton. In contrast, N ≥3 -layer MoTe2 exhibits a much reduced photoluminescence quantum yield and a broader, redshifted, and seemingly bimodal photoluminescence spectrum. The low- and high-energy contributions are attributed to emission from the indirect and direct optical band gaps, respectively. Bulk MoTe2 displays a broad emission line with a dominant contribution at 0.94 eV that is assigned to emission from the indirect optical band gap. As compared to related systems (such as MoS2,MoSe2,WS2, and WSe2), the smaller energy difference between the monolayer direct optical band gap and the bulk indirect optical band gap leads to a smoother increase of the photoluminescence quantum yield as N decreases. In addition, we study the evolution of the photoluminescence intensity in monolayer MoTe2 as a function of the exciton formation rate Wabs up to 3.6 ×1022cm-2s-1 . The line shape of the photoluminescence spectrum remains largely independent of Wabs, whereas the photoluminescence intensity grows sublinearly above Wabs˜1021cm-2s-1 . This behavior is assigned to exciton-exciton annihilation and is well captured by an elementary rate equation model.

  8. Inductively coupled plasma-atomic emission spectroscopy: a computer controlled, scanning monochromator system for the rapid determination of the elements

    SciTech Connect

    Floyd, M.A.

    1980-03-01

    A computer controlled, scanning monochromator system specifically designed for the rapid, sequential determination of the elements is described. The monochromator is combined with an inductively coupled plasma excitation source so that elements at major, minor, trace, and ultratrace levels may be determined, in sequence, without changing experimental parameters other than the spectral line observed. A number of distinctive features not found in previously described versions are incorporated into the system here described. Performance characteristics of the entire system and several analytical applications are discussed.

  9. Modes competition in superradiant emission from an inverted sub-wavelength thick slab of two-level atoms

    NASA Astrophysics Data System (ADS)

    Manassah, Jamal T.

    2016-08-01

    Using the expansion in the eigenmodes of 1-D Lienard-Wiechert kernel, the temporal and spectral profiles of the radiation emitted by a fully inverted collection of two-level atoms in a sub-wavelength slab geometry are computed. The initial number of amplifying modes determine the specific regime of radiation. In particular, the temporal profile of the field intensity is oscillatory and the spectral profile is non-Lorentzian with two unequal height peaks in a narrow band centered at the slab thickness value at which the real parts of the lowest order odd and even eigenvalues are equal.

  10. Determination of iron, cobalt, nickel, manganese, zinc, copper, cadmium and lead in human hair by inductively coupled plasma-atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Sreenivasa Rao, K.; Balaji, T.; Prasada Rao, T.; Babu, Y.; Naidu, G. R. K.

    2002-08-01

    A method was standardized for the dissolution of hair samples and analysis was carried out by inductively coupled plasma atomic emission spectrometry (ICP-AES). Hair samples were brought into solution by using a mixture of nitric acid and hydrogen peroxide. Various parameters that influence the sample preparation, namely temperature, digestion time and ratio of acid mixture were studied and standardized. The optimized method has been employed to digest standard reference materials and hair samples of residents of India, collected from different age groups and sex, and analyzed for Fe, Co, Ni, Mn, Zn, Cu, Cd and Pb. The values agree for most of the metals with the data reported for human hair samples of residents of India. The NIES CRM Human Hair No. 5 and IAEA Reference Hair HH-1 certified reference materials were used in order to verify the accuracy of the method and the results were in excellent agreement with the certified values.

  11. Laser based analysis using a passively Q-switched laser employing analysis electronics and a means for detecting atomic optical emission of the laser media

    DOEpatents

    Woodruff, Steven D.; Mcintyre, Dustin L.

    2016-03-29

    A device for Laser based Analysis using a Passively Q-Switched Laser comprising an optical pumping source optically connected to a laser media. The laser media and a Q-switch are positioned between and optically connected to a high reflectivity mirror (HR) and an output coupler (OC) along an optical axis. The output coupler (OC) is optically connected to the output lens along the optical axis. A means for detecting atomic optical emission comprises a filter and a light detector. The optical filter is optically connected to the laser media and the optical detector. A control system is connected to the optical detector and the analysis electronics. The analysis electronics are optically connected to the output lens. The detection of the large scale laser output production triggers the control system to initiate the precise timing and data collection from the detector and analysis.

  12. Pressure dissolution and real sample matrix calibration for multielement analysis of raw agricultural crops by inductively coupled plasma atomic emission spectrometry

    SciTech Connect

    Kuennen, R.W.; Woinik, K.A.; Fricke, F.L.; Caruso, J.A.

    1982-11-01

    A method utilizing a pressure dissolution technique to minimize sample pretreatment is described for multielement analysis of raw agricultural crops by inductively coupled argon plasma atomic emission spectrometry. The procedure employs a 30-min pressure dissolution of sample composite with 6 M HCI at 80/sup 8/C in 60-mL linear polyethylene bottles. A sample introduction system is also described which permits direct atomization of complex organic matrices. Combined with a real sample matrix callbration technique, this introduction system allows rapid and accurate multielement analysis of complex HCl sample matrix solutions. The procedure compares favorably to more time-consuming conventional wet ashing methods for the determination of major, minor, and trace elements occurring in lettuce, potatoes, peanuts, soybeans, spinach, sweet corn, and wheat. Recoveries for spiked samples, precision studies, and analyses of NBS reference materials demonstrate the reliability and accuracy of the procedure. Advantages and limitations of this technique relative to conventional wet ashing methods are discussed. 2 figures, 7 tables.

  13. Thermospheric atomic oxygen concentrations from WINDII O+(2P→2D) 732 nm emission: Comparisons with the NRLMSISE-00 and C-IAM models and with GUVI observations

    NASA Astrophysics Data System (ADS)

    Shepherd, Gordon G.; Cho, Young-Min; Fomichev, Victor I.; Martynenko, Oleg V.

    2016-09-01

    Thermospheric atomic oxygen concentrations have been retrieved from observations by the Wind Imaging Interferometer (WINDII) O+(2P→2D) 732 and 733 nm emissions and are compared with results obtained by the Global Ultraviolet Imager (GUVI). Although the observations compared were taken ten years apart, the periods were selected on the basis of solar activity, using the Canadian Ionosphere and Atmosphere Model (C-IAM) to bridge the time gap. Results from all of these were compared with those from the Naval Research Laboratory Mass Spectrometer and Incoherent Scatter (NRLMSISE-00) model. Comparisons were made on the basis of F10.7 solar flux, day of year, local time, season, latitude and longitude. The WINDII local time variations showed enhanced values for the Northern spring season. Latitude and longitude plots showed smooth variations for NRLMSISE-00 and large variations for both WINDII and GUVI observations; in particular a depression in atomic oxygen concentration around 40 °S latitude and 100 °E longitude that is tentatively identified with a longitudinal wave 1 that does not propagate in local time but has an annual variation. The averaged values showed the WINDII values to be 0.75 that of NRLMSISE-00 compared with 0.80 for GUVI. Thus the WINDII values agreed with those of GUVI to within 6%, although taken 10 years apart.

  14. The emission of energetic electrons from atoms by fast ions considered as a charge-transfer process

    NASA Astrophysics Data System (ADS)

    Miraglia, J. E.; Ponce, V. H.

    1980-03-01

    The ejection of energetic electrons from atoms by fast ions is described using as final electron states the continuum orbitals in the field of the projectile. The electronic distribution in the first-order Born approximation is equal to the distribution for direct ionisation where the final electron state is described by a plane wave times the Coulomb factor centred on the projectile. In the second-order Born approximation the distribution of ejected electrons is significantly decreased, and it is shown that it is equivalent to the correct distribution for direct ionisation in first order times the Coulomb factor around the projectile. For the case of ejected electrons with negligible momentum in the frame of the projectile, it is shown that the electron distribution centered on the projectile is isotropic to order v to the -12th, while the double scattering term in v to the -11th depends on the direction of motion of the electron.

  15. A Simple Model to Quantify Radiolytic Production following Electron Emission from Heavy-Atom Nanoparticles Irradiated in Liquid Suspensions.

    PubMed

    Wardlow, Nathan; Polin, Chris; Villagomez-Bernabe, Balder; Currell, Fred

    2015-11-01

    We present a simple model for a component of the radiolytic production of any chemical species due to electron emission from irradiated nanoparticles (NPs) in a liquid environment, provided the expression for the G value for product formation is known and is reasonably well characterized by a linear dependence on beam energy. This model takes nanoparticle size, composition, density and a number of other readily available parameters (such as X-ray and electron attenuation data) as inputs and therefore allows for the ready determination of this contribution. Several approximations are used, thus this model provides an upper limit to the yield of chemical species due to electron emission, rather than a distinct value, and this upper limit is compared with experimental results. After the general model is developed we provide details of its application to the generation of HO• through irradiation of gold nanoparticles (AuNPs), a potentially important process in nanoparticle-based enhancement of radiotherapy. This model has been constructed with the intention of making it accessible to other researchers who wish to estimate chemical yields through this process, and is shown to be applicable to NPs of single elements and mixtures. The model can be applied without the need to develop additional skills (such as using a Monte Carlo toolkit), providing a fast and straightforward method of estimating chemical yields. A simple framework for determining the HO• yield for different NP sizes at constant NP concentration and initial photon energy is also presented. PMID:26488757

  16. A Simple Model to Quantify Radiolytic Production following Electron Emission from Heavy-Atom Nanoparticles Irradiated in Liquid Suspensions.

    PubMed

    Wardlow, Nathan; Polin, Chris; Villagomez-Bernabe, Balder; Currell, Fred

    2015-11-01

    We present a simple model for a component of the radiolytic production of any chemical species due to electron emission from irradiated nanoparticles (NPs) in a liquid environment, provided the expression for the G value for product formation is known and is reasonably well characterized by a linear dependence on beam energy. This model takes nanoparticle size, composition, density and a number of other readily available parameters (such as X-ray and electron attenuation data) as inputs and therefore allows for the ready determination of this contribution. Several approximations are used, thus this model provides an upper limit to the yield of chemical species due to electron emission, rather than a distinct value, and this upper limit is compared with experimental results. After the general model is developed we provide details of its application to the generation of HO• through irradiation of gold nanoparticles (AuNPs), a potentially important process in nanoparticle-based enhancement of radiotherapy. This model has been constructed with the intention of making it accessible to other researchers who wish to estimate chemical yields through this process, and is shown to be applicable to NPs of single elements and mixtures. The model can be applied without the need to develop additional skills (such as using a Monte Carlo toolkit), providing a fast and straightforward method of estimating chemical yields. A simple framework for determining the HO• yield for different NP sizes at constant NP concentration and initial photon energy is also presented.

  17. A miniaturized capacitively coupled plasma microtorch optical emission spectrometer and a Rh coiled-filament as small-sized electrothermal vaporization device for simultaneous determination of volatile elements from liquid microsamples: spectral and analytical characterization.

    PubMed

    Frentiu, Tiberiu; Darvasi, Eugen; Butaciu, Sinziana; Ponta, Michaela; Petreus, Dorin; Mihaltan, Alin I; Frentiu, Maria

    2014-11-01

    A low power and low argon consumption (13.56 MHz, 15 W, 150 ml min(-1)) capacitively coupled plasma microtorch interfaced with a low-resolution microspectrometer and a small-sized electrothermal vaporization Rh coiled-filament as liquid microsample introduction device into the plasma was investigated for the simultaneous determination of several volatile elements of interest for environment. Constructive details, spectral and analytical characteristics, and optimum operating conditions of the laboratory equipment for the simultaneous determination of Ag, Cd, Cu, Pb and Zn requiring low vaporization power are provided. The method involves drying of 10 μl sample at 100°C, vaporization at 1500°C and emission measurement by capture of 20 successive spectral episodes each at an integration time of 500 ms. Experiments showed that emission of elements and plasma background were disturbed by the presence of complex matrix and hot Ar flow transporting the microsample into plasma. The emission spectrum of elements is simple, dominated by the resonance lines. The analytical system provided detection limits in the ng ml(-1) range: 0.5(Ag); 1.5(Cd); 5.6(Cu); 20(Pb) and 3(Zn) and absolute detection limits of the order of pg: 5(Ag); 15(Cd); 56(Cu); 200(Pb) and 30(Zn). It was demonstrated the utility and capability of the miniaturized analytical system in the simultaneous determination of elements in soil and water sediment using the standard addition method to compensate for the non-spectral effects of alkali and earth alkaline elements. The analysis of eight certified reference materials exhibited reliable results with recovery in the range of 95-108% and precision of 0.5-9.0% for the five examined elements. The proposed miniaturized analytical system is attractive due to the simple construction of the electrothermal vaporization device and microtorch, low costs associated to plasma generation, high analytical sensitivity and easy-to-run for simultaneous multielemental

  18. Analysis of an atom laser based on the spatial control of the scattering length

    SciTech Connect

    Carpentier, Alicia V.; Michinel, Humberto; Rodas-Verde, Maria I.; Perez-Garcia, Victor M.

    2006-07-15

    In this paper we analyze atom lasers based on the spatial modulation of the scattering length of a Bose-Einstein condensate. We demonstrate, through numerical simulations and approximate analytical methods, the controllable emission of matter-wave bursts and study the dependence of the process on the spatial shape of the scattering length along the axis of emission. We also study the role of an additional modulation of the scattering length in time.

  19. Measurement of Trace Metals in Tobacco and Cigarette Ash by Inductively Coupled Plasma-Atomic Emission Spectroscopy

    NASA Astrophysics Data System (ADS)

    Wang, W.; Finlayson-Pitts, B. J.

    2003-01-01

    The ICP AES experiment reported here is suitable for use in a junior- or senior-level undergraduate instrumental analysis laboratory. The objective of this experiment is to analyze trace metals present in cigarette tobacco, the cigarette filter, and the ash obtained when the cigarette is burned. Two different brands of cigarettes, one with and one without a filter, were used. The filter was analyzed before and after smoke was drawn through it. The trace metals were extracted using concentrated nitric acid at room temperature and at 100 °C respectively, to test the extraction efficiency. Some tobacco samples were spiked with ZnCl2 and FeCl3 to assess the efficiency of the recovery. Zinc and iron are shown to be present in tobacco, filter, and ash, while chromium was above the detection limit only in the ash. These metals are concentrated in the ash compared to the tobacco by factors of ˜4 (Zn), 12 17 (Fe), and ≥ 2 (Cr). If sufficient laboratory time is available, this experiment could be paired with one using atomic absorption (AA) to demonstrate the advantages and disadvantages of ICP when compared to AA.

  20. A non-statistical atomic model for beam emission and motional Stark effect diagnostics in fusion plasmas.

    PubMed

    Ralchenko, Yu; Marchuk, O; Biel, W; Schlummer, T; Schultz, D R; Stambulchik, E

    2012-10-01

    In this work we analyze magnetic sublevel populations in a neutral beam penetrating a fusion plasma. The collisional-radiative model NOMAD was extended to include magnetic parabolic sublevels with principal quantum numbers n ≤ 10. The collisional parameters were calculated with the advanced atomic-orbital close coupling method and the Glauber approximation. The ionization by the induced electric field was also included in the model. The results of our calculations show significant deviations of the sublevel populations and, accordingly, line intensities of the σ and π components, from the statistical approximation. It is shown, for instance, that for a number of experimental conditions the total intensity of σ components is not equal to the total intensity of π components, which has a strong effect on determination of magnetic field and pitch angle in fusion devices. The results are presented for a wide range of plasma and beam parameters. The most significant deviations are observed for strong magnetic fields and high beam energies typical for the ITER plasma, where component intensity ratios may deviate by more than 20% from the statistical values.

  1. Developments in glow discharge emission spectrometry

    NASA Astrophysics Data System (ADS)

    Ferreira, N. P.; Strauss, J. A.; Human, H. G. C.

    Developments in the field of glow discharge emission spectrometry at the National Physical Research Laboratory of the Council for Scientific and Industrial Research comprise measurement of fundamental plasma parameters, instrumental development and analytical applications. While reference is only made to published material, recent developments are described in more detail, e.g. the use of a fluorescent atomic vapour as spectral line isolator and the use of a microwave auxiliary discharge to augment excitation of sputtered material.

  2. An integrated analytical framework for quantifying the LCOE of waste-to-energy facilities for a range of greenhouse gas emissions policy and technical factors.

    PubMed

    Townsend, Aaron K; Webber, Michael E

    2012-07-01

    This study presents a novel integrated method for considering the economics of waste-to-energy (WTE) facilities with priced greenhouse gas (GHG) emissions based upon technical and economic characteristics of the WTE facility, MSW stream, landfill alternative, and GHG emissions policy. The study demonstrates use of the formulation for six different policy scenarios and explores sensitivity of the results to ranges of certain technical parameters as found in existing literature. The study shows that details of the GHG emissions regulations have large impact on the levelized cost of energy (LCOE) of WTE and that GHG regulations can either increase or decrease the LCOE of WTE depending on policy choices regarding biogenic fractions from combusted waste and emissions from landfills. Important policy considerations are the fraction of the carbon emissions that are priced (i.e. all emissions versus only non-biogenic emissions), whether emissions credits are allowed due to reducing fugitive landfill gas emissions, whether biogenic carbon sequestration in landfills is credited against landfill emissions, and the effectiveness of the landfill gas recovery system where waste would otherwise have been buried. The default landfill gas recovery system effectiveness assumed by much of the industry yields GHG offsets that are very close to the direct non-biogenic GHG emissions from a WTE facility, meaning that small changes in the recovery effectiveness cause relatively larger changes in the emissions factor of the WTE facility. Finally, the economics of WTE are dependent on the MSW stream composition, with paper and wood being advantageous, metal and glass being disadvantageous, and plastics, food, and yard waste being either advantageous or disadvantageous depending upon the avoided tipping fee and the GHG emissions price. PMID:22425189

  3. An integrated analytical framework for quantifying the LCOE of waste-to-energy facilities for a range of greenhouse gas emissions policy and technical factors.

    PubMed

    Townsend, Aaron K; Webber, Michael E

    2012-07-01

    This study presents a novel integrated method for considering the economics of waste-to-energy (WTE) facilities with priced greenhouse gas (GHG) emissions based upon technical and economic characteristics of the WTE facility, MSW stream, landfill alternative, and GHG emissions policy. The study demonstrates use of the formulation for six different policy scenarios and explores sensitivity of the results to ranges of certain technical parameters as found in existing literature. The study shows that details of the GHG emissions regulations have large impact on the levelized cost of energy (LCOE) of WTE and that GHG regulations can either increase or decrease the LCOE of WTE depending on policy choices regarding biogenic fractions from combusted waste and emissions from landfills. Important policy considerations are the fraction of the carbon emissions that are priced (i.e. all emissions versus only non-biogenic emissions), whether emissions credits are allowed due to reducing fugitive landfill gas emissions, whether biogenic carbon sequestration in landfills is credited against landfill emissions, and the effectiveness of the landfill gas recovery system where waste would otherwise have been buried. The default landfill gas recovery system effectiveness assumed by much of the industry yields GHG offsets that are very close to the direct non-biogenic GHG emissions from a WTE facility, meaning that small changes in the recovery effectiveness cause relatively larger changes in the emissions factor of the WTE facility. Finally, the economics of WTE are dependent on the MSW stream composition, with paper and wood being advantageous, metal and glass being disadvantageous, and plastics, food, and yard waste being either advantageous or disadvantageous depending upon the avoided tipping fee and the GHG emissions price.

  4. An integrated analytical framework for quantifying the LCOE of waste-to-energy facilities for a range of greenhouse gas emissions policy and technical factors

    SciTech Connect

    Townsend, Aaron K.; Webber, Michael E.

    2012-07-15

    This study presents a novel integrated method for considering the economics of waste-to-energy (WTE) facilities with priced greenhouse gas (GHG) emissions based upon technical and economic characteristics of the WTE facility, MSW stream, landfill alternative, and GHG emissions policy. The study demonstrates use of the formulation for six different policy scenarios and explores sensitivity of the results to ranges of certain technical parameters as found in existing literature. The study shows that details of the GHG emissions regulations have large impact on the levelized cost of energy (LCOE) of WTE and that GHG regulations can either increase or decrease the LCOE of WTE depending on policy choices regarding biogenic fractions from combusted waste and emissions from landfills. Important policy considerations are the fraction of the carbon emissions that are priced (i.e. all emissions versus only non-biogenic emissions), whether emissions credits are allowed due to reducing fugitive landfill gas emissions, whether biogenic carbon sequestration in landfills is credited against landfill emissions, and the effectiveness of the landfill gas recovery system where waste would otherwise have been buried. The default landfill gas recovery system effectiveness assumed by much of the industry yields GHG offsets that are very close to the direct non-biogenic GHG emissions from a WTE facility, meaning that small changes in the recovery effectiveness cause relatively larger changes in the emissions factor of the WTE facility. Finally, the economics of WTE are dependent on the MSW stream composition, with paper and wood being advantageous, metal and glass being disadvantageous, and plastics, food, and yard waste being either advantageous or disadvantageous depending upon the avoided tipping fee and the GHG emissions price.

  5. A continuous flow cold vapour procedure for mercury determination by atomic emission using the reverse flow injection approach

    NASA Astrophysics Data System (ADS)

    De Andrade, João Carlos; Bueno, Maria Izabel M. S.

    1994-07-01

    An experimental set-up for on-line Hg 2+ reduction and determination was devised using the reverse flow injection analysis (r-FIA) concept and the cold vapour (CV) technique, injecting an acidic Sn 2+ solution into the mercury sample line. The elemental mercury generated is separated from the reacting mixture by a 100 ml min -1 helium stream, which passes through a gas-liquid separator connected to a permeation cell. This gas stream is used as the plasma medium. The permeated Hg° is then concentrated on a 0.3 g gold foil placed inside a quartz tube connected to an 11 W He de discharge plasma chamber. The mercury retained on the gold surface is released by resistive heating and the emission intensity is observed at the 253.7 nm mercury line. For an injection cycle of 30 s, the calibration graphs are linear up to 50 ng ml -1(itr 2 = 0.999). An injection frequency of 120 h -1 is achieved, with negligible carry-over. The calculated relative standard deviation of the transient peaks is 1.6%. Higher sensitivities can be achieved using longer injection cycles. Samples of Human Hair Certified Reference Material were used to determine the accuracy of the method.

  6. Resonant nonstationary amplification of polychromatic laser pulses and conical emission in an optically dense ensemble of neon metastable atoms

    NASA Astrophysics Data System (ADS)

    Bagayev, S. N.; Egorov, V. S.; Mekhov, I. B.; Moroshkin, P. V.; Chekhonin, I. A.; Davliatchine, E. M.; Kindel, E.

    2003-10-01

    Experimental and numerical investigation of single-beam and pump-probe interaction with a resonantly absorbing dense extended medium under strong and weak field-matter coupling is presented. Significant probe beam amplification and conical emission were observed. Under relatively weak pumping and high medium density, when the condition of strong coupling between field and resonant matter is fulfilled, the probe amplification spectrum has a form of spectral doublet. Stronger pumping leads to the appearance of a single peak of the probe beam amplification at the transition frequency. The greater probe intensity results in an asymmetrical transmission spectrum with amplification at the blue wing of the absorption line and attenuation at the red one. Under high medium density, a broadband of amplification appears. The theoretical model is based on the solution of the Maxwell-Bloch equations for a two-level system. Different types of probe transmission spectra obtained are attributed to complex dynamics of a coherent medium response to broadband polychromatic radiation of a multimode dye laser.

  7. [Research Progress in Analytical Technology for Heavy Metals in Atmospheric Particles].

    PubMed

    Wang, Yu-jie; Tu, Zhen-quan; Zhou, Li; Chi, Yong-jie; Luo, Qin

    2015-04-01

    Atmospheric particles have become the primary atmospheric pollutions, of which the heavy metals, owing to non-degradability and hysteresis, a serious threat to human life and natural environment, have become a hot research issue currently. The analytical methods of heavy metals in atmospheric particles are summarized in the present review, including atomic absorption spectrometry, inductively coupled plasma atomic emission spectrometry, inductively coupled plasma mass spectrometry, neutron activation analysis, fluorescence spectrometry, glow discharge atomic emission spectrometry, microwave plasma atomic emission spectrometry, and laser induced breakdown spectroscopy, and some proposals are tried to make for improving the shortcomings of these technologies: continuum source Atomic absorption spectrometry for simultaneously measuring multi-elements, atomic emission spectrometry for direct determination of particulates, high resolution laser ablation inductively coupled plasma mass spectrometry for determination of solid samples, low scattering synchrotron fluorescence spectrum for determination of atmospheric particulate matter and k0 neutron activation analysis for determination of radioactive elements in the troposphere Analysis techniques of heavy metals in atmospheric particulate matter are promoted to develop toward being real-time, fast, low- detection-limit, direct-measurement and simple-operation due to the spatial and temporal distribution difference of the heavy metals in atmospheric particles and human requirement for improvement of ambient air quality as well as rapid development of modern instrument science and technology. PMID:26197596

  8. High-temperature liquid chromatography inductively coupled plasma atomic emission spectrometry hyphenation for the combined organic and inorganic analysis of foodstuffs.

    PubMed

    Terol, Amanda; Paredes, Eduardo; Maestre, Salvador E; Prats, Soledad; Todolí, José L

    2010-10-01

    The coupling of a High-Temperature Liquid Chromatography system (HTLC) with an Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES) is reported for the first time. This hyphenation combines the separation efficiency of HTLC with the detection power of a simultaneous ICP-AES system and allows the combined determination of organic compound and metals. The effluents of the column were introduced into the spectrometer and the chromatograms for organic compounds were obtained by plotting the carbon emission signal at a characteristic wavelength versus time. As regards metals, they were determined by injecting a small sample volume between the exit of the column and the spectrometer and taking the emission intensity for each one of the elements simultaneously. Provided that in HTLC the effluents emerged at high temperatures, an aerosol was easily generated at the exit of the column. Therefore, the use of a pneumatic nebulizer as a component of a liquid sample introduction system in the ICP-AES could be avoided, thus reducing the peak dispersion and limits of detection by a factor of two. The fact that a hot liquid stream was nebulized made it necessary to use a thermostated spray chamber so as to avoid the plasma cooling as a cause of the excessive mass of solvent delivered to it. Due to the similarity in sample introduction, an Evaporative Light Scattering Detector (ELSD) was taken as a reference. Comparatively speaking, limits of detection were of the same order for both HTLC-ICP-AES and HTLC-ELSD, although the latter provided better results for some compounds (from 10 to 20 mg L(-1) and 5-10 mg L(-1), respectively). In contrast, the dynamic range for the new hyphenation was about two orders of magnitude wider. More importantly, HTLC-ICP-AES provided information about the content of both organic (glucose, sucrose, maltose and lactose at concentrations from roughly 10 to 400 mg L(-1)) as well as inorganic (magnesium, calcium, sodium, zinc, potassium and

  9. Analytical Chemistry Laboratory Progress Report for FY 1994

    SciTech Connect

    Green, D.W.; Boparai, A.S.; Bowers, D.L.

    1994-12-01

    The purpose of this report is to summarize the activities of the Analytical Chemistry Laboratory (ACL) at Argonne National Laboratory (ANL) for Fiscal Year (FY) 1994 (October 1993 through September 1994). This annual report is the eleventh for the ACL and describes continuing effort on projects, work on new projects, and contributions of the ACL staff to various programs at ANL. The Analytical Chemistry Laboratory is a full-cost-recovery service center, with the primary mission of providing a broad range of analytical chemistry support services to the scientific and engineering programs at ANL. The ACL also has a research program in analytical chemistry, conducts instrumental and methods development, and provides analytical services for governmental, educational, and industrial organizations. The ACL handles a wide range of analytical problems. Some routine or standard analyses are done, but it is common for the Argonne programs to generate unique problems that require significant development of methods and adaption of techniques to obtain useful analytical data. The ACL has four technical groups -- Chemical Analysis, Instrumental Analysis, Organic Analysis, and Environmental Analysis -- which together include about 45 technical staff members. Talents and interests of staff members cross the group lines, as do many projects within the ACL. The Chemical Analysis Group uses wet- chemical and instrumental methods for elemental, compositional, and isotopic determinations in solid, liquid, and gaseous samples and provides specialized analytical services. Major instruments in this group include an ion chromatograph (IC), an inductively coupled plasma/atomic emission spectrometer (ICP/AES), spectrophotometers, mass spectrometers (including gas-analysis and thermal-ionization mass spectrometers), emission spectrographs, autotitrators, sulfur and carbon determinators, and a kinetic phosphorescence uranium analyzer.

  10. Multielement determination of heavy metals in water samples by continuous powder introduction microwave-induced plasma atomic emission spectrometry after preconcentration on activated carbon

    NASA Astrophysics Data System (ADS)

    Jankowski, Krzysztof; Yao, Jun; Kasiura, Krzysztof; Jackowska, Adrianna; Sieradzka, Anna

    2005-03-01

    A novel continuous powder introduction microwave-induced plasma atomic emission spectrometry method (CPI-MIP-AES) has been developed for trace determination of metals in ground and tap water samples after preconcentration on activated carbon. The experimental setup consisted of integrated rectangular cavity TE 101 and vertically positioned plasma torch. The technical arrangement of the sample introduction system has been designed based on the fluidized bed concept. The satisfactory signal stability required for sequential analysis was attained owing to the vertical plasma configuration, as well as the plasma gas flow rate compatibility with sample introduction flow rate. The elements of interest (Cd, Cu, Cr, Fe, Mn, Pb, Zn) were preconcentrated in a batch procedure at pH 8-8.5 after addition of activated carbon and then, after filtering and drying of the activated carbon suspension, introduced to the MIP by the CPI system. An enrichment factor of about 1000-fold for a sample volume of 1 l was obtained. The detection limit values for the proposed method were 17-250 ng l -1. The proposed method was validated by analyzing the certified reference materials: SRW "Warta" Synthetic River Water and BCR CRM 399 major elements in freshwater. The method was successfully applied to the determination of the heavy metals in tap water samples.

  11. Determination of white phosphorus residues in ducks: An atomic emission detection/compound-independent calibration-based method of generating residue data for risk assessment and environmental monitoring

    SciTech Connect

    Johnston, J.J.; Goldade, D.A.; Kohler, D.J.; Cummings, J.L.

    2000-05-01

    Analysis of phosphorus concentrations in the gizzards of ducks harvested from munitions sites is necessary to ascertain if acute phosphorus toxicity was the cause of death and to estimate potential secondary hazards to predators and scavengers, such as eagles that readily consume the dead ducks. Gas chromatography-atomic emission detection analysis permitted compound-independent quantification of white phosphorus standards following analysis of the stable phosphorus-containing compound triethyl phosphate. The white phosphorus standards were then used to quantify white phosphorus residues in duck gizzard extracts by gas chromatography-flame photometric detection analysis. For gizzards containing less than 0.01 {micro}g of phosphorus, quantification was based on a three-point calibration curve. For gizzards containing 0.01 {micro}g or more of white phosphorus, single-point calibration was used. Mean recoveries for phosphorus-fortified gizzards ranged from 73 to 91%. The method limit of detection was 0.013 {micro}g of phosphorus. This method was successfully applied to the quantification of white phosphorus in ducks collected from Eagle River Flats, AK. Potential applications to risk assessment and environmental monitoring are also discussed.

  12. Evaluation of flow injection-solution cathode glow discharge-atomic emission spectrometry for the determination of major elements in brines.

    PubMed

    Yang, Chun; Wang, Lin; Zhu, Zhenli; Jin, Lanlan; Zheng, Hongtao; Belshaw, Nicholas Stanley; Hu, Shenghong

    2016-08-01

    A new method for the determination of major metal elements in high salinity brines was developed by solution cathode glow discharge (SCGD) with flow injection analysis (FIA). The matrix interferences of major cations and anions in brines have been evaluated. It was found that high concentration of Na(+) and K(+) could interfere each other, K(+) at a concentration of 400mgL(-1) enhanced the signal intensity of Na(+) more than 20%. The effect of the anions was observed and it was noted that the signal intensity of both Ca(2+) and Mg(2+) were suppressed significantly when the SO4(2-) reached 100mgL(-1). It was demonstrated that some low molecular weight organic substances such as formic acid, glycerol and ascorbic acid could eliminate interference of SO4(2-) even with volume percentages of 0.5%. Under the optimized condition, the proposed FIA-SCGD can determine K, Na, Ca and Mg with the limits of detection of 0.49 (K), 0.14 (Na), 11 (Ca) and 5.5 (Mg) ngmL(-1). The proposed method has been successfully applied to the analysis of 5 salt lake samples and compared with those obtained with inductively coupled plasma atomic emission spectrometry (ICP-AES). The advantages of small size, low energy consumption, good stability and repeatability indicated that the SCGD is promising for the determination of major ions in brine samples. PMID:27216688

  13. Simple and robust method for lithium traces determination in drinking water by atomic emission using low-power capacitively coupled plasma microtorch and microspectrometer.

    PubMed

    Zsigmond, Andreea R; Frentiu, Tiberiu; Ponta, Michaela; Frentiu, Maria; Petreus, Dorin

    2013-12-15

    A method for Li determination in drinking water using atomic emission spectrometry in a new low-power Ar capacitively coupled plasma microtorch (15 W, 0.6 L min(-1)) with a detection limit of 0.013 μg L(-1) was developed. The method is based on external calibration in the presence of a buffering solution containing 5 mg L(-1) Na, K, Ca, Mg added both to calibration standards and water samples. The statistical validation on 31 bottled drinking water samples (0.4-2140 μg L(-1) Li) using the Bland and Altman test and regression analysis has shown results similar to those obtained by the standard additions method. The buffering solution approach is simpler than the standard additions and has demonstrated good intra- and interday precision, accuracy and robustness. It was successfully applied over a wide concentration range of Li and multimineral matrix with a pooled precision of 2.5-3.5% and 99±9% accuracy.

  14. A pulsed source for Xe(6s[3/2]1) and Xe(6s'[1/2]1) resonance state atoms using two-photon driven amplified spontaneous emission from the Xe(6p) and Xe(6p') states

    NASA Astrophysics Data System (ADS)

    Alekseev, V. A.; Setser, D. W.

    1996-09-01

    A new, simple method for the generation of Xe(6s[3/2]1) and Xe(6s'[1/2]1) atoms is described. The method involves resonant two-photon excitation of Xe(6p[1/2]0 and 6p'[3/2]2) states followed by amplified spontaneous emission (ASE) to the Xe(6s[3/2]1 and 6s'[1/2]1) states. The vacuum ultraviolet transitions, Xe(6s[3/2]1→5p6(1S0)) at 147 nm and Xe(6s'[1/2]1→5p6(1S0)) at 129.6 nm, were used to monitor the time dependence of the resonance state atom concentrations. The quenching rate constants of these resonance atoms with ten molecules were measured at 300 K. The quenching cross-sections of the Xe(6s and 6s') resonance atoms are compared to the cross-sections of the metastable Xe(6s[3/2]2) atoms and Xe(6p[3/2]2) atoms. The correlation between quenching cross-sections and photoabsorption cross-section of the molecules predicted by the resonance dipole-dipole energy transfer model is discussed. The applicability of the two-photon driven ASE method for the generation of other resonance state atoms is considered.

  15. Improved graphite furnace atomizer

    DOEpatents

    Siemer, D.D.

    1983-05-18

    A graphite furnace atomizer for use in graphite furnace atomic absorption spectroscopy is described wherein the heating elements are affixed near the optical path and away from the point of sample deposition, so that when the sample is volatilized the spectroscopic temperature at the optical path is at least that of the volatilization temperature, whereby analyteconcomitant complex formation is advantageously reduced. The atomizer may be elongated along its axis to increase the distance between the optical path and the sample deposition point. Also, the atomizer may be elongated along the axis of the optical path, whereby its analytical sensitivity is greatly increased.

  16. Optical diagnostics of radio-frequency plasmas containing CHF3 and CHF3/O2: Laser-induced fluorescence of CF2, CF, and O atoms, and optical emission from H, F, and O

    NASA Astrophysics Data System (ADS)

    Hancock, G.; Sucksmith, J. P.

    2002-01-01

    Laser-induced fluorescence (LIF) has been used to measure absolute concentrations of CF2, CF, and O atoms in a parallel-plate capacitatively coupled radio-frequency-driven plasma containing CHF3 and its mixtures with Ar and O2 at pressures between 50 and 500 mTorr. In CHF3 the spatial distribution of CF2 peaks at the driven electrode, and shows the importance of surface processes for its production. Time-resolved studies show evidence for its homogeneous chemical removal. CF concentrations are an order of magnitude lower than those of CF2, and removal by reaction with H atoms is consistent with time-resolved data taken on plasma extinction. For both radicals the absolute concentrations are higher than those found for similar plasmas in CF4. In the presence of O2 the fluorinated radical concentrations drop to below the detection limit, and the influence of surface removal processes is again invoked to explain the increase in O atom concentration observed when a small amount of CHF3 is added to a dominantly O2 gas flow. Optical emission from excited F, H, and O atoms is observed, and even when corrected by actinometry, is shown to be an unreliable indicator of the relative concentration of the ground-state species because of contributions from dissociative excitation of stable species in the discharge. Excited H atoms are found to be translationally hot from measurements of their linewidths, and are clearly not all formed from excitation of H atoms. Time-resolved actinometry (TRA) can be used in some cases to remove the contribution to the emission from dissociative excitation, but in the case of O atoms where both LIF and TRA were compared, the influence of a time-dependent dissociative excitation step complicates the analysis and is attributed to the presence of other species such as O2(a1Δg) in the discharge.

  17. The CHIANTI atomic database

    NASA Astrophysics Data System (ADS)

    Young, P. R.; Dere, K. P.; Landi, E.; Del Zanna, G.; Mason, H. E.

    2016-04-01

    The freely available CHIANTI atomic database was first released in 1996 and has had a huge impact on the analysis and modeling of emissions from astrophysical plasmas. It contains data and software for modeling optically thin atom and positive ion emission from low density (≲1013 cm-3) plasmas from x-ray to infrared wavelengths. A key feature is that the data are assessed and regularly updated, with version 8 released in 2015. Atomic data for modeling the emissivities of 246 ions and neutrals are contained in CHIANTI, together with data for deriving the ionization fractions of all elements up to zinc. The different types of atomic data are summarized here and their formats discussed. Statistics on the impact of CHIANTI to the astrophysical community are given and examples of the diverse range of applications are presented.

  18. The use of ion chromatography-dc plasma atomic emission spectrometry for the speciation of trace metals. Annual performance report, February 1, 1989--January 31, 1992

    SciTech Connect

    Urasa, I.T.

    1991-09-20

    The original objects of this research program were: to interface d.c. plasma atomic emission spectrometer with an ion chromatograph; to characterize and optimize the combined systems for application in the speciation of metals in aqueous solutions; to use this system in the study of the solution chemistry of various metals; and to find ways in which the measurement sensitivity of the method can be enhanced, thereby allowing the detection of metal species at low ppb concentration levels. This approach has been used to study the chemistry of and speciate several elements in solution including: arsenic, chromium, iron, manganese, nickel phosphorus, platinum, selenium, and vanadium. During the course of this research, we have found that the solution chemistry of the elements studied and the speciation data obtained can vary considerably depending on the solution, and the chromatographic conditions employed. The speciation of chromium, iron, and vanadium was found to be highly influenced by the acidity of the sample. The element selective nature of the d.c. plasma detector allows these changes to be monitored, thereby providing quantitative information on the new moieties formed. New approaches are being developed including the use of chelating ligands as preconcentration agents for purposes of reducing further the detection limits of the elements of interest and to improve the overall element speciation scheme. New thrusts are being directed towards the employment of post-column derivatization method coupled with colorimetric measurements to detect and quantify metal species eluting from the chromatographic column. The influence of sample acidity on these investigations will be carefully evaluated. These new thrusts are described in the accompanying Project Renewal Proposal.

  19. UNCERTAINTIES IN ATOMIC DATA AND THEIR PROPAGATION THROUGH SPECTRAL MODELS. I

    SciTech Connect

    Bautista, M. A.; Fivet, V.; Quinet, P.; Dunn, J.; Gull, T. R.; Kallman, T. R.; Mendoza, C.

    2013-06-10

    We present a method for computing uncertainties in spectral models, i.e., level populations, line emissivities, and emission line ratios, based upon the propagation of uncertainties originating from atomic data. We provide analytic expressions, in the form of linear sets of algebraic equations, for the coupled uncertainties among all levels. These equations can be solved efficiently for any set of physical conditions and uncertainties in the atomic data. We illustrate our method applied to spectral models of O III and Fe II and discuss the impact of the uncertainties on atomic systems under different physical conditions. As to intrinsic uncertainties in theoretical atomic data, we propose that these uncertainties can be estimated from the dispersion in the results from various independent calculations. This technique provides excellent results for the uncertainties in A-values of forbidden transitions in [Fe II].

  20. Analytical testing

    NASA Technical Reports Server (NTRS)

    Flannelly, W. G.; Fabunmi, J. A.; Nagy, E. J.

    1981-01-01

    Analytical methods for combining flight acceleration and strain data with shake test mobility data to predict the effects of structural changes on flight vibrations and strains are presented. This integration of structural dynamic analysis with flight performance is referred to as analytical testing. The objective of this methodology is to analytically estimate the results of flight testing contemplated structural changes with minimum flying and change trials. The category of changes to the aircraft includes mass, stiffness, absorbers, isolators, and active suppressors. Examples of applying the analytical testing methodology using flight test and shake test data measured on an AH-1G helicopter are included. The techniques and procedures for vibration testing and modal analysis are also described.

  1. 40 CFR 91.312 - Analytical gases.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 20 2014-07-01 2013-07-01 true Analytical gases. 91.312 Section 91.312... EMISSIONS FROM MARINE SPARK-IGNITION ENGINES Emission Test Equipment Provisions § 91.312 Analytical gases. (a) The shelf life of a calibration gas may not be exceeded. Record the expiration date stated by...

  2. Micro-Crater Laser Induced Breakdown Spectroscopy--an Analytical approach in metals samples

    SciTech Connect

    Piscitelli, Vincent; Gonzalez, Jhanis; Mao Xianglei; Russo, Richard; Fernandez, Alberto

    2008-04-15

    The laser ablation has been increasing its popularity like as technique of chemical analysis. This is due to its great potentiality in the analysis of solid samples. On the way to contributing to the development of the technique, we in this work studied the laser induced breakdown spectroscopy (LIBS) in conditions of micro ablation for future studies of coverings and micro crates analysis. Craters between 2 and 7 micrometers of diameter were made using an Nd-YAG nanosecond laser in their fundamental emission of 1064 nm. In order to create these craters we use an objective lens of long distance work and 0.45 of numerical aperture. The atomic emission versus the energy of the laser and its effect on the size of craters was study. We found that below 3 micrometers although there was evidence of material removal by the formation of a crater, it was no detectable atomic emission for our instruments. In order to try to understand this, curves of size of crater versus plasma temperature using the Boltzmann distribution graphs taking the Copper emission lines in the visible region were made. In addition calibration curves for Copper and aluminum were made in two different matrices; one of it was a Cu/Zn alloy and the other a Zinc Matrix. The atomic lines Cu I (521.78 nm) and Al I (396.15 nm) was used. From the Calibration curve the analytical limit of detection and other analytical parameters were obtained.

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

    NASA Astrophysics Data System (ADS)

    Matos, Wladiana O.; Menezes, Eveline A.; Gonzalez, Mário H.; Costa, Letícia M.; Trevizan, Lilian C.; Nogueira, Ana Rita A.

    2009-06-01

    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 µL. 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 4-1 fractional factorial design: 650 W microwave power, 7 min digestion time, 50 µL 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.

  4. Fraunhofer effect atomic absorption spectrometry.

    PubMed

    Rust, Jennifer A; Nóbrega, Joaquim A; Calloway, Clifton P; Jones, Bradley T

    2005-02-15

    The dark lines in the solar spectrum were discovered by Wollaston and cataloged by Fraunhofer in the early days of the 19th century. Some years later, Kirchhoff explained the appearance of the dark lines: the sun was acting as a continuum light source and metals in the ground state in its atmosphere were absorbing characteristic narrow regions of the spectrum. This discovery eventually spawned atomic absorption spectrometry, which became a routine technique for chemical analysis in the mid-20th century. Laboratory-based atomic absorption spectrometers differ from the original observation of the Fraunhofer lines because they have always employed a separate light source and atomizer. This article describes a novel atomic absorption device that employs a single source, the tungsten coil, as both the generator of continuum radiation and the atomizer of the analytes. A 25-microL aliquot of sample is placed on the tungsten filament removed from a commercially available 150-W light bulb. The solution is dried and ashed by applying low currents to the coil in a three-step procedure. Full power is then applied to the coil for a brief period. During this time, the coil produces white light, which may be absorbed by any metals present in the atomization cloud produced by the sample. A high-resolution spectrometer with a charge-coupled device detector monitors the emission spectrum of the coil, which includes the dark lines from the metals. Detection limits are reported for seven elements: 5 pg of Ca (422.7 nm); 2 ng of Co (352.7 nm); 200 pg of Cr (425.4 nm); 7 pg of Sr (460.7 nm); 100 pg of Yb (398.8 nm); 500 pg of Mn (403.1 nm); and 500 pg of K (404.4 nm). Simultaneous multielement analyses are possible within a 4-nm spectral window. The relative standard deviations for the seven metals are below 8% for all metals except for Ca (10.7%), which was present in the blank at measurable levels. Analysis of a standard reference material (drinking water) resulted in a mean percent

  5. Analytical Microscopy

    SciTech Connect

    Not Available

    2006-06-01

    In the Analytical Microscopy group, within the National Center for Photovoltaic's Measurements and Characterization Division, we combine two complementary areas of analytical microscopy--electron microscopy and proximal-probe techniques--and use a variety of state-of-the-art imaging and analytical tools. We also design and build custom instrumentation and develop novel techniques that provide unique capabilities for studying materials and devices. In our work, we collaborate with you to solve materials- and device-related R&D problems. This sheet summarizes the uses and features of four major tools: transmission electron microscopy, scanning electron microscopy, the dual-beam focused-ion-beam workstation, and scanning probe microscopy.

  6. Analytical Technology

    SciTech Connect

    Goheen, Steven C.

    2001-07-01

    Characterizing environmental samples has been exhaustively addressed in the literature for most analytes of environmental concern. One of the weak areas of environmental analytical chemistry is that of radionuclides and samples contaminated with radionuclides. The analysis of samples containing high levels of radionuclides can be far more complex than that of non-radioactive samples. This chapter addresses the analysis of samples with a wide range of radioactivity. The other areas of characterization examined in this chapter are the hazardous components of mixed waste, and special analytes often associated with radioactive materials. Characterizing mixed waste is often similar to characterizing waste components in non-radioactive materials. The largest differences are in associated safety precautions to minimize exposure to dangerous levels of radioactivity. One must attempt to keep radiological dose as low as reasonably achievable (ALARA). This chapter outlines recommended procedures to safely and accurately characterize regulated components of radioactive samples.

  7. Atom-assisted quadrature squeezing of a mechanical oscillator inside a dispersive cavity

    NASA Astrophysics Data System (ADS)

    Chauhan, Anil Kumar; Biswas, Asoka

    2016-08-01

    We present a hybrid optomechanical scheme to achieve dynamical squeezing of position quadrature of a mesoscopic mechanical oscillator, that can be externally controlled by classical fields. A membrane-in-the-middle setup is employed, in which an atom in Λ configuration is considered to be trapped on either side of the membrane inside the cavity. We show that a considerable amount of squeezing (beyond the 3-dB limit) can be achieved and maintained at a transient time scale that is not affected by the spontaneous emission of the atom. Squeezing depends upon the initial preparation of atomic states. Further, a strong effective coupling (larger than the relevant decay rates) between the atom and the oscillator can be attained by using large control fields that pump the atom and the cavity. The effects of cavity decay and the phononic bath on squeezing are studied. The results are supported by the detailed analytical calculations.

  8. ISOTROPIC INELASTIC COLLISIONS IN A MULTITERM ATOM WITH HYPERFINE STRUCTURE

    SciTech Connect

    Belluzzi, Luca; Landi Degl’Innocenti, Egidio; Bueno, Javier Trujillo

    2015-10-10

    A correct modeling of the scattering polarization profiles observed in some spectral lines of diagnostic interest, the sodium doublet being one of the most important examples, requires taking hyperfine structure (HFS) and quantum interference between different J-levels into account. An atomic model suitable for taking these physical ingredients into account is the so-called multiterm atom with HFS. In this work, we introduce and study the transfer and relaxation rates due to isotropic inelastic collisions with electrons, which enter the statistical equilibrium equations (SEE) for the atomic density matrix of this atomic model. Under the hypothesis that the electron–atom interaction is described by a dipolar operator, we provide useful relations between the rates describing the transfer and relaxation of quantum interference between different levels (whose numerical values are in most cases unknown) and the usual rates for the atomic level populations, for which experimental data and/or approximate theoretical expressions are generally available. For the particular case of a two-term atom with HFS, we present an analytical solution of the SEE for the spherical statistical tensors of the upper term, including both radiative and collisional processes, and we derive the expression of the emission coefficient in the four Stokes parameters. Finally, an illustrative application to the Na i D{sub 1} and D{sub 2} lines is presented.

  9. Solving a Mock Arsenic-Poisoning Case Using Atomic Spectroscopy

    NASA Astrophysics Data System (ADS)

    Tarr, Matthew A.

    2001-01-01

    A new upper-level undergraduate atomic spectroscopy laboratory procedure has been developed that presents a realistic problem to students and asks them to assist in solving it. Students are given arsenic-laced soda samples from a mock crime scene. From these samples, they are to gather evidence to help prosecute a murder suspect. The samples are analyzed by inductively coupled plasma atomic emission spectroscopy or by atomic absorbance spectroscopy to determine the content of specific metal impurities. By statistical comparison of the samples' composition, the students determine if the soda samples can be linked to arsenic found in the suspect's home. As much as possible, the procedures and interpretations are developed by the students. Particular emphasis is placed on evaluating the limitations and capabilities of the analytical method with respect to the demands of the problem.

  10. Development of a microcartridge technique for the measurement of atmospheric carbonyls and emissions from plants and a new analytical technique for the measurement of argon as a passive tracer

    NASA Astrophysics Data System (ADS)

    Skaggs, Rhonda Lynn

    A new cartridge sampling and derivatization technique was developed for the determination of aldehydes and ketones in air that allows measurement of sub-ppbv mixing ratios using sampling times of ten minutes or less. This thesis describes the development and evaluation of the analytical technique and a preliminary survey of carbonyl emissions from wounded plants. Also described is the development of an analytical technique for the measurement of argon, a passive biogeochemical tracer. Carbonyl compounds are sampled onto high pressure cartridges containing particles coated with 2,4- dinitrophenylhydrazine where they react to form hydrazones. The entire sample is eluted and transferred to the head of a high performance liquid chromatograph (HPLC) for separation and detection by UV absorbance. The method is demonstrated to be approximately two orders of magnitude more sensitive than the conventional DNPH technique in which only a small fraction of the hydrazones are transferred to the column. It was found that two calibration methods gave different sensitivities resulting from the formation of different ratios of syn and anti isomers of the hydrazones. These results suggest that many measurements of atmospheric carbonyls reported in the literature may have significant errors if syn and anti isomers were unresolved. A chamber method was used to study the emissions of aldehydes and ketones from a variety of wounded plants. 2-E-Hexenal and acetaldehyde were detected in the wound response emissions of all six plants examined. Enhanced concentrations of methylethyl ketone (MEK) in addition to acetaldehyde and 2-E-hexenal were detected following wounding of clover, and the emissions of 2-E-hexenal and MEK in response to wounding displayed different temporal release patterns. A novel application of a commercial photionization detector for the quantification of argon is described and applied to the headspace analysis of water. Argon is measured indirectly by its effect on an

  11. Nuclear Waste Analytical Round Robins 1-6 summary report

    SciTech Connect

    Smith, G.L.; Marschman, S.C.

    1993-12-31

    The MCC has conducted six round robins for the waste management, research, and development community from 1987 to present. The laboratories participating regularly are Ames, Argonne, Catholic University, Lawrence Livermore, Pacific Northwest Laboratory, Savannah River, and West Valley Nuclear. Glass types analyzed in these round robins all have been simulated nuclear waste compositions expected from vitrification of high-level nuclear waste. A wide range of analytical procedures have been used by the participating laboratories including Atomic Absorption spectroscopy, inductively coupled plasma-atomic emission spectroscopy, direct current plasma-emission spectroscopy, and inductively coupled plasma-mass spectroscopy techniques. Consensus average relative error for Round Robins 1 through 6 is 5.4%, with values ranging from 9.4 to 1.1%. Trend on the average improved with each round robin. When the laboratories analyzed samples over longer periods of time, the intralaboratory variability increased. Lab-to-lab variation accounts for most of the total variability found in all the round robins. Participation in the radiochemistry portion has been minimal, and analytical results poor compared to nonradiochemistry portion. Additional radiochemical work is needed in future round robins.

  12. Atomic scale investigations on Cd{sub x}Zn{sub 1−x}Se quantum dots: Correlation between the composition and emission properties

    SciTech Connect

    Benallali, H. Hoummada, K.; Mangelinck, D.; Cremel, T.; André, R.; Tatarenko, S.; Kheng, K.

    2014-08-04

    Atom probe tomography and photoluminescence spectroscopy have been used to study Cd{sub x}Zn{sub 1−x}Se quantum dots embedded in a ZnSe layer grown on a (001) GaAs substrate. Atom probe tomography analyses show significant cadmium incorporation in the center of the dots surrounded by poor cadmium region. These measurements illustrate that the maximum cadmium concentration in the quantum dots is significantly higher than the concentration estimated by transmission electron microscopy. The composition and size of quantum dots obtained by atom probe tomography have been used to calculate the transition energies including excitonic and strain effects.

  13. Analytical chemistry of nickel.

    PubMed

    Stoeppler, M

    1984-01-01

    Analytical chemists are faced with nickel contents in environmental and biological materials ranging from the mg/kg down to the ng/kg level. Sampling and sample treatment have to be performed with great care at lower levels, and this also applies to enrichment and separation procedures. The classical determination methods formerly used have been replaced almost entirely by different forms of atomic absorption spectrometry. Electroanalytical methods are also of increasing importance and at present provide the most sensitive approach. Despite the powerful methods available, achieving reliable results is still a challenge for the analyst requiring proper quality control measures.

  14. Atom beams split by gentle persuasion

    SciTech Connect

    Pool, R.

    1994-02-25

    Two different research teams have taken a big step toward atom interferometry. They have succeeded in splitting atomic beams by using atoms in spin states that neither absorb nor reemit laser light. By proper adjustment of experimental conditions, atoms are changed from one spin state to another, without passing through the intermediary excited state. The atoms in essence absorb momentum from the laser photons, without absorption or emission of photons. The change in momentum deflects atoms in the proper spin state.

  15. Chemometrics-assisted excitation-emission fluorescence analytical data for rapid and selective determination of optical brighteners in the presence of uncalibrated interferences

    NASA Astrophysics Data System (ADS)

    Gholami, Ali; Masoum, Saeed; Mohsenikia, Atefeh; Abbasi, Saleheh

    2016-01-01

    This study describes a novel approach for the simultaneous determination of CBS-X and CXT as widely used optical brighteners in household detergent, by combining the advantage of the high sensitivity of molecular fluorescence, and the selectivity of second-order chemometric methods. The proposed method is assisted by second-order chemometric analyses employing the PARAFAC, SWATLD and APTLD that help us to determine CBS-X and CXT in laundry powders and environmental samples, through the unique decomposition of the three-way data array. Proposed method can provide the extraction of relative concentrations of the analytes, as well as the spectral profiles. This approach achieves the second-order advantage and in principle could be able to overcome the spectral uncalibrated interference problems in the determination of CBS-X and CXT at the ng g- 1 level. By spiking the known concentrations of these compounds to the real samples, the accuracy of the proposed methods was validated and recoveries of the spiked values were calculated. High recoveries (90.00%-113.33%) for the spiked laundry powders and real environmental samples indicate the present method successfully faces this complex challenge without the necessity of applying separation and preconcentration steps in environmental contaminations.

  16. Analytic H i-to-H2 Photodissociation Transition Profiles

    NASA Astrophysics Data System (ADS)

    Bialy, Shmuel; Sternberg, Amiel

    2016-05-01

    We present a simple analytic procedure for generating atomic (H i) to molecular ({{{H}}}2) density profiles for optically thick hydrogen gas clouds illuminated by far-ultraviolet radiation fields. Our procedure is based on the analytic theory for the structure of one-dimensional H i/{{{H}}}2 photon-dominated regions, presented by Sternberg et al. Depth-dependent atomic and molecular density fractions may be computed for arbitrary gas density, far-ultraviolet field intensity, and the metallicity-dependent H2 formation rate coefficient, and dust absorption cross section in the Lyman–Werner photodissociation band. We use our procedure to generate a set of {{H}} {{I}}{-}{to}{-}{{{H}}}2 transition profiles for a wide range of conditions, from the weak- to strong-field limits, and from super-solar down to low metallicities. We show that if presented as functions of dust optical depth, the {{H}} {{I}} and {{{H}}}2 density profiles depend primarily on the Sternberg “α G parameter” (dimensionless) that determines the dust optical depth associated with the total photodissociated {{H}} {{I}} column. We derive a universal analytic formula for the {{H}} {{I}}{-}{to}{-}{{{H}}}2 transition points as a function of just α G. Our formula will be useful for interpreting emission-line observations of H i/{{{H}}}2 interfaces, for estimating star formation thresholds, and for sub-grid components in hydrodynamics simulations.

  17. Analytic H i-to-H2 Photodissociation Transition Profiles

    NASA Astrophysics Data System (ADS)

    Bialy, Shmuel; Sternberg, Amiel

    2016-05-01

    We present a simple analytic procedure for generating atomic (H i) to molecular ({{{H}}}2) density profiles for optically thick hydrogen gas clouds illuminated by far-ultraviolet radiation fields. Our procedure is based on the analytic theory for the structure of one-dimensional H i/{{{H}}}2 photon-dominated regions, presented by Sternberg et al. Depth-dependent atomic and molecular density fractions may be computed for arbitrary gas density, far-ultraviolet field intensity, and the metallicity-dependent H2 formation rate coefficient, and dust absorption cross section in the Lyman-Werner photodissociation band. We use our procedure to generate a set of {{H}} {{I}}{-}{to}{-}{{{H}}}2 transition profiles for a wide range of conditions, from the weak- to strong-field limits, and from super-solar down to low metallicities. We show that if presented as functions of dust optical depth, the {{H}} {{I}} and {{{H}}}2 density profiles depend primarily on the Sternberg “α G parameter” (dimensionless) that determines the dust optical depth associated with the total photodissociated {{H}} {{I}} column. We derive a universal analytic formula for the {{H}} {{I}}{-}{to}{-}{{{H}}}2 transition points as a function of just α G. Our formula will be useful for interpreting emission-line observations of H i/{{{H}}}2 interfaces, for estimating star formation thresholds, and for sub-grid components in hydrodynamics simulations.

  18. Analytical sedimentology

    SciTech Connect

    Lewis, D.W. . Dept. of Geology); McConchie, D.M. . Centre for Coastal Management)

    1994-01-01

    Both a self instruction manual and a cookbook'' guide to field and laboratory analytical procedures, this book provides an essential reference for non-specialists. With a minimum of mathematics and virtually no theory, it introduces practitioners to easy, inexpensive options for sample collection and preparation, data acquisition, analytic protocols, result interpretation and verification techniques. This step-by-step guide considers the advantages and limitations of different procedures, discusses safety and troubleshooting, and explains support skills like mapping, photography and report writing. It also offers managers, off-site engineers and others using sediments data a quick course in commissioning studies and making the most of the reports. This manual will answer the growing needs of practitioners in the field, either alone or accompanied by Practical Sedimentology, which surveys the science of sedimentology and provides a basic overview of the principles behind the applications.

  19. The Kinetics of Nitrogen Atom Recombination

    ERIC Educational Resources Information Center

    Brown, G. Ronald; Winkler, C. A.

    1977-01-01

    Describes a study of the kinetics of the recombination of nitrogen atoms in which concentration-time relations are determined directly by utilizing visual observations of emissions to make gas phase titrations of N atoms with NO. (MLH)

  20. 40 CFR 600.108-08 - Analytical gases.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 31 2012-07-01 2012-07-01 false Analytical gases. 600.108-08 Section... ECONOMY AND GREENHOUSE GAS EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures § 600.108-08 Analytical gases. The analytical gases for all fuel economy...

  1. 40 CFR 600.108-08 - Analytical gases.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 31 2013-07-01 2013-07-01 false Analytical gases. 600.108-08 Section... ECONOMY AND GREENHOUSE GAS EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures § 600.108-08 Analytical gases. The analytical gases for all fuel economy...

  2. 40 CFR 600.108-08 - Analytical gases.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 30 2014-07-01 2014-07-01 false Analytical gases. 600.108-08 Section... ECONOMY AND GREENHOUSE GAS EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures § 600.108-08 Analytical gases. The analytical gases for all fuel economy...

  3. Visualization of atom's orbits.

    PubMed

    Kim, Byungwhan

    2014-02-01

    High-resolution imaging techniques have been used to obtain views of internal shapes of single atoms or columns of atoms. This review article focuses on the visualization of internal atomic structures such as the configurations of electron orbits confined to atoms. This is accomplished by applying visualization techniques to the reported images of atoms or molecules as well as static and dynamic ions in a plasma. It was found that the photon and electron energies provide macroscopic and microscopic views of the orbit structures of atoms, respectively. The laser-imaged atoms showed a rugged orbit structure, containing alternating dark and bright orbits believed to be the pathways for an externally supplied laser energy and internally excited electron energy, respectively. By contrast, the atoms taken by the electron microscopy provided a structure of fine electron orbits, systematically formed in increasing order of grayscale representing the energy state of an orbit. This structure was identical to those of the plasma ions. The visualized electronic structures played a critical role in clarifying vague postulates made in the Bohr model. Main features proposed in the atomic model are the dynamic orbits absorbing an externally supplied electromagnetic energy, electron emission from them while accompanying light radiation, and frequency of electron waves not light. The light-accompanying electrons and ionic speckles induced by laser light signify that light is composed of electrons and ions.

  4. Retrieval of atomic oxygen and temperature in the thermosphere. Part 1: Feasibility of an experiment based on the spectrally resolved 147 micrometer limb emission

    NASA Astrophysics Data System (ADS)

    Zachor, A. S.; Sharma, R. D.; Yap, B. K.; Riehl, J. P.

    1989-04-01

    The importance of atomic oxygen and translational temperature in mesospheric/thermospheric processes is the motivation to study the feasibility of recovering vertical profiles of the temperature and O-atom density from limb scan data obtained near 147 micrometer and/or 63 micrometer wavelength, corresponding to the oxygen atom ground electronic state (OI) transitions. The limb radiance data must be spectrally resolved to recover both temperature and atomic oxygen density if only one of the OI lines is used, which is the approach investigated in this report. We show how the two vertical profiles can be recovered by applying an onion-peeling method to synthetic data. The temperature and O-atom density in each peeled layer are obtained simultaneously by nonlinear least-squares spectrum fitting. Spectral data in the 147 micrometer line was found to yield reasonably accurate and stable profiles from 300 km down to an altitude between 130 and 90 km, depending on the noise level and spectral resolution, and gave better results than the stronger 63 micrometer data below 140 km. We estimate that the S/N and spectral resolution required for successful retrievals could be provided by a confocal Fabry-Perot system operating near 147 micrometer although retrievals down to 90 km from data obtained at orbital altitude would require cooled foreoptics roughly a meter in diameter.

  5. Simultaneous multielement atomic absorption spectrometry with graphite furnace atomization

    NASA Astrophysics Data System (ADS)

    Harnly, James M.; Miller-Ihli, Nancy J.; O'Haver, Thomas C.

    The extended analytical range capability of a simultaneous multielement atomic absorption continuum source spectrometer (SIMAAC) was tested for furnace atomization with respect to the signal measurement mode (peak height and area), the atomization mode (from the wall or from a platform), and the temperature program mode (stepped or ramped atomization). These parameters were evaluated with respect to the shapes of the analytical curves, the detection limits, carry-over contamination and accuracy. Peak area measurements gave more linear calibration curves. Methods for slowing the atomization step heating rate, the use of a ramped temperature program or a platform, produced similar calibration curves and longer linear ranges than atomization with a stepped temperature program. Peak height detection limits were best using stepped atomization from the wall. Peak area detection limits for all atomization modes were similar. Carry-over contamination was worse for peak area than peak height, worse for ramped atomization than stepped atomization, and worse for atomization from a platform than from the wall. Accurate determinations (100 ± 12% for Ca, Cu, Fe, Mn, and Zn in National Bureau of Standards' Standard Reference Materials Bovine Liver 1577 and Rice Flour 1568 were obtained using peak area measurements with ramped atomization from the wall and stepped atomization from a platform. Only stepped atomization from a platform gave accurate recoveries for K. Accurate recoveries, 100 ± 10%, with precisions ranging from 1 to 36 % (standard deviation), were obtained for the determination of Al, Co, Cr, Fe, Mn, Mo, Ni. Pb, V and Zn in Acidified Waters (NBS SRM 1643 and 1643a) using stepped atomization from a platform.

  6. High-order harmonic emission in bowtie-shaped nanostructure with few-cycle spatially inhomogeneous laser fields when the atom is placed at different spatial positions

    NASA Astrophysics Data System (ADS)

    Luo, Xiang-Yi; Wang, Tian; Wang, Qun; Liu, Xue-Shen

    2016-11-01

    In this study, we investigate the harmonic spectra in the vicinity of the center of the nanostructure gap when helium atom is placed at different spatial positions. We find that the high-order harmonic spectra is very sensitive to the atomic spatial positions in a inhomogeneous laser field. When the initial atomic spatial position is changed from  ‑9.0 a.u. to 9.0 a.u., the cutoff of the high-order harmonic generation (HHG) can be extended, and the supercontinuum harmonic spectrum of the second plateau is extended to the high-order and the low-order simultaneously. The HHG process is demonstrated by using the time-frequency analysis, the semi-classical three-step model and the ionization probability.

  7. Analytical toxicology.

    PubMed

    Flanagan, R J; Widdop, B; Ramsey, J D; Loveland, M

    1988-09-01

    1. Major advances in analytical toxicology followed the introduction of spectroscopic and chromatographic techniques in the 1940s and early 1950s and thin layer chromatography remains important together with some spectrophotometric and other tests. However, gas- and high performance-liquid chromatography together with a variety of immunoassay techniques are now widely used. 2. The scope and complexity of forensic and clinical toxicology continues to increase, although the compounds for which emergency analyses are needed to guide therapy are few. Exclusion of the presence of hypnotic drugs can be important in suspected 'brain death' cases. 3. Screening for drugs of abuse has assumed greater importance not only for the management of the habituated patient, but also in 'pre-employment' and 'employment' screening. The detection of illicit drug administration in sport is also an area of increasing importance. 4. In industrial toxicology, the range of compounds for which blood or urine measurements (so called 'biological monitoring') can indicate the degree of exposure is increasing. The monitoring of environmental contaminants (lead, chlorinated pesticides) in biological samples has also proved valuable. 5. In the near future a consensus as to the units of measurement to be used is urgently required and more emphasis will be placed on interpretation, especially as regards possible behavioural effects of drugs or other poisons. Despite many advances in analytical techniques there remains a need for reliable, simple tests to detect poisons for use in smaller hospital and other laboratories.

  8. Analytical Chemistry and the Microchip.

    ERIC Educational Resources Information Center

    Lowry, Robert K.

    1986-01-01

    Analytical techniques used at various points in making microchips are described. They include: Fourier transform infrared spectrometry (silicon purity); optical emission spectroscopy (quantitative thin-film composition); X-ray photoelectron spectroscopy (chemical changes in thin films); wet chemistry, instrumental analysis (process chemicals);…

  9. Atomic characterization of Si nanoclusters embedded in SiO2 by atom probe tomography.

    PubMed

    Roussel, Manuel; Talbot, Etienne; Gourbilleau, Fabrice; Pareige, Philippe

    2011-02-23

    Silicon nanoclusters are of prime interest for new generation of optoelectronic and microelectronics components. Physical properties (light emission, carrier storage...) of systems using such nanoclusters are strongly dependent on nanostructural characteristics. These characteristics (size, composition, distribution, and interface nature) are until now obtained using conventional high-resolution analytic methods, such as high-resolution transmission electron microscopy, EFTEM, or EELS. In this article, a complementary technique, the atom probe tomography, was used for studying a multilayer (ML) system containing silicon clusters. Such a technique and its analysis give information on the structure at the atomic level and allow obtaining complementary information with respect to other techniques. A description of the different steps for such analysis: sample preparation, atom probe analysis, and data treatment are detailed. An atomic scale description of the Si nanoclusters/SiO2 ML will be fully described. This system is composed of 3.8-nm-thick SiO layers and 4-nm-thick SiO2 layers annealed 1 h at 900°C.

  10. Atomic characterization of Si nanoclusters embedded in SiO2 by atom probe tomography.

    PubMed

    Roussel, Manuel; Talbot, Etienne; Gourbilleau, Fabrice; Pareige, Philippe

    2011-01-01

    Silicon nanoclusters are of prime interest for new generation of optoelectronic and microelectronics components. Physical properties (light emission, carrier storage...) of systems using such nanoclusters are strongly dependent on nanostructural characteristics. These characteristics (size, composition, distribution, and interface nature) are until now obtained using conventional high-resolution analytic methods, such as high-resolution transmission electron microscopy, EFTEM, or EELS. In this article, a complementary technique, the atom probe tomography, was used for studying a multilayer (ML) system containing silicon clusters. Such a technique and its analysis give information on the structure at the atomic level and allow obtaining complementary information with respect to other techniques. A description of the different steps for such analysis: sample preparation, atom probe analysis, and data treatment are detailed. An atomic scale description of the Si nanoclusters/SiO2 ML will be fully described. This system is composed of 3.8-nm-thick SiO layers and 4-nm-thick SiO2 layers annealed 1 h at 900°C. PMID:21711666

  11. The Stair-Step Atom.

    ERIC Educational Resources Information Center

    Jordan, Thomas M.; And Others

    1992-01-01

    Presents a model of a generic atom that is used to represent the movement of electrons from lower to higher levels and vice-versa due to excitation and de-excitation of the atom. As the process of de-excitation takes place, photons represented by colored ping-pong balls are emitted, indicating the emission of light. (MDH)

  12. Master equation with quantized atomic motion including dipole-dipole interactions

    NASA Astrophysics Data System (ADS)

    Damanet, François; Braun, Daniel; Martin, John

    2016-05-01

    We derive a markovian master equation for the internal dynamics of an ensemble of two-level atoms including all effects related to the quantization of their motion. Our equation provides a unifying picture of the consequences of recoil and indistinguishability of atoms beyond the Lamb-Dicke regime on both their dissipative and conservative dynamics, and is relevant for experiments with ultracold trapped atoms. We give general expressions for the decay rates and the dipole-dipole shifts for any motional states, and we find analytical formulas for a number of relevant states (Gaussian states, Fock states and thermal states). In particular, we show that the dipole-dipole interactions and cooperative photon emission can be modulated through the external state of motion. The effects predicted should be experimentally observable with Rydberg atoms. FD would like to thank the F.R.S.-FNRS for financial support. FD is a FRIA Grant holder of the Fonds de la Recherche Scientifique-FNRS.

  13. Determination of vanadium in petroleum and petroleum products using atomic spectrometric techniques.

    PubMed

    Amorim, Fábio A C; Welz, Bernhard; Costa, Antônio C S; Lepri, Fábio G; Vale, Maria Goreti R; Ferreira, Sérgio L C

    2007-04-30

    Vanadium is recognized worldwide as the most abundant metallic constituent in petroleum. It is causing undesired side effects in the refining process, and corrosion in oil-fired power plants. Consequently, it is the most widely determined metal in petroleum and its derivatives. This paper offers a critical review of analytical methods based on atomic spectrometric techniques, particularly flame atomic absorption spectrometry (FAAS), electrothermal atomic absorption spectrometry (ET AAS), inductively coupled plasma optical emission spectrometry (ICP OES), inductively coupled plasma mass spectrometry (ICP-MS). In addition an overview is provided of the sample pretreatment and preparation procedures for vanadium determination in petroleum and petroleum products. Also included are the most recent studies about speciation and fractionation analysis using atomic spectrometric techniques.

  14. Applicability of solid-phase microextraction combined with gas chromatography atomic emission detection (GC-MIP AED) for the determination of butyltin compounds in sediment samples.

    PubMed

    Carpinteiro, J; Rodríguez, I; Cela, R

    2004-11-01

    The performance of solid-phase microextraction (SPME) applied to the determination of butyltin compounds in sediment samples is systematically evaluated. Matrix effects and influence of blank signals on the detection limits of the method are studied in detail. The interval of linear response is also evaluated in order to assess the applicability of the method to sediments polluted with butyltin compounds over a large range of concentrations. Advantages and drawbacks of including an SPME step, instead of the classic liquid-liquid extraction of the derivatized analytes, in the determination of butyltin compounds in sediment samples are considered in terms of achieved detection limits and experimental effort. Analytes were extracted from the samples by sonication using glacial acetic acid. An aliquot of the centrifuged extract was placed on a vial where compounds were ethylated and concentrated on a PDMS fiber using the headspace mode. Determinations were carried out using GC-MIP AED. PMID:15365677

  15. ENDOCRINE DISRUPTING CHEMICAL EMISSIONS FROM COMBUSTION SOURCES: DIESEL PARTICULATE EMISSIONS AND DOMESTIC WASTE OPEN BURN EMISSIONS

    EPA Science Inventory

    Emissions of endocrine disrupting chemicals (EDCs) from combustion sources are poorly characterized due to the large number of compounds present in the emissions, the complexity of the analytical separations required, and the uncertainty regarding identification of chemicals with...

  16. Retrieval of atomic oxygen and temperature in the thermosphere. I - Feasibility of an experiment based on the spectrally resolved 147 micron limb emission

    NASA Astrophysics Data System (ADS)

    Zachor, A. S.; Sharma, R. D.

    1989-11-01

    Consideration is given to the possibility of recovering vertical profiles of the temperature and O-atom density from limb scan data obtained near 147 and/or 63 microns wavelength. It is shown that the two vertical profiles may be recovered by applying an onion-peeling method to synthetic data. The temperature and O-atom density are obtained simultaneously by a nonlinear least-squares spectrum fitting. It is found that spectral data in the 147-micron line from 300 km down to 130-90 km in altitude produces better results than the 63-micron data below 140 km. It is suggested that a confocal Fabry-Perot system operating near 147 microns could provide the S/N ratio and spectral resolution needed for successful retrievals. Retrievals down to 90 km from data obtained at orbital altitude would require cooled foreoptics with a diameter of about 1 meter.

  17. The use of ion chromatography-D.C. plasma atomic emission spectrometry for the speciation of trace metals. Final performance technical report, February 1, 1995--January 31, 1998

    SciTech Connect

    Urasa, I.T.

    1998-06-12

    The chemistry of heavy metals in natural waters, industrial waste streams, and the environment is influenced by a number of factors including the prevailing matrix, their relative concentrations, and biologically or chemically induced transformations. Speciation, which entails the identification and quantification of all the forms of a metal or any other chemical entity present in a sample, is a necessary step in assessing the toxic and pollution effects and the overall impact of these entities on environmental systems. Analytical methods and protocols that can provide analytical data in the parts per billion concentration range and below are needed for these kinds of measurements. The thrust of this research was to develop metal speciation methods and techniques using direct current plasma (DCPAES) in combination with ion chromatography (IC), whereby the DCPAES serves as an element selective detector (ESD) for the metal species separated in the chromatographic column. While the metal speciation work carried out in this program has utilized the IC-DCPAES as the primary analytical measurement tool, other sample processing and preparation approaches have also been developed to enhance the effectiveness and capability of the chromatographic-element selective method of metal speciation. Post-column derivatization and solid phase extraction are two protocols which were incorporated with IC-ESD with significant improvements in the capability of the method.

  18. Spontaneous emission and the operation of invisibility cloaks

    NASA Astrophysics Data System (ADS)

    Morshed Behbahani, Mina; Amooghorban, Ehsan; Mahdifar, Ali

    2016-07-01

    As a probe to explore the ability of invisibility cloaks to conceal objects in the quantum mechanics domain, we study the spontaneous emission rate of an excited two-level atom in the vicinity of an ideal invisibility cloaking. On this base, first, a canonical quantization scheme is presented for the electromagnetic field interacting with atomic systems in an anisotropic, inhomogeneous, and absorbing magnetodielectric medium which can suitably be used for studying the influence of arbitrary invisibility cloak on the atomic radiative properties. The time dependence of the atomic subsystem is obtained in the Schrodinger picture. By introducing a modified set of the spherical wave-vector functions, the Green tensor of the system is calculated via exact and discrete methods. In this formalism, the decay rate and as well the emission pattern of the aforementioned atom are computed analytically for both weak and strong coupling interaction, and then numerically calculations are done to demonstrate the performances of cloaking in the quantum mechanics domain. Special attention is paid to different possible orientations and locations of the atomic system near the spherical invisibility cloaking. Results in the presence and the absence of the invisibility cloak are compared. We find that the cloak works very well far from its resonance frequency to conceal a macroscopic object, whereas at near the resonance frequency the object is more visible than the situation where the object is not covered by the cloak.

  19. Measurement of the parity violating 6S-7S transition amplitude in cesium achieved within 2×10-13 atomic-unit accuracy by stimulated-emission detection

    NASA Astrophysics Data System (ADS)

    Guéna, J.; Lintz, M.; Bouchiat, M. A.

    2005-04-01

    We exploit the process of asymmetry amplification by stimulated emission which provides an original method for parity violation (PV) measurements in a highly forbidden atomic transition. The method involves measurements of a chiral, transient, optical gain of a cesium vapor on the 7S-6P3/2 transition, probed after it is excited by an intense, linearly polarized, collinear laser, tuned to resonance for one hyperfine line of the forbidden 6S-7S transition in a longitudinal electric field. We report here a 3.5-fold increase of the one-second-measurement sensitivity and subsequent reduction by a factor of 3.5 of the statistical accuracy compared with our previous result [J. Guéna , Phys. Rev. Lett. 90, 143001 (2003)]. Decisive improvements to the setup include an increased repetition rate, better extinction of the probe beam at the end of the probe pulse, and, for the first time to our knowledge, the following: a polarization-tilt magnifier, quasisuppression of beam reflections at the cell windows, and a Cs cell with electrically conductive windows. We also present real-time tests of systematic effects and consistency checks on the data, as well as a 1% accurate measurement of the electric field seen by the atoms, from atomic signals. PV measurements performed in seven different vapor cells agree within the statistical error. Our present result is compatible with the more precise result of Wood within our present relative statistical accuracy of 2.6%, corresponding to a 2×10-13 atomic-unit uncertainty in E1pv . Theoretical motivations for further measurements are emphasized and we give a brief overview of a recent proposal that would allow the uncertainty to be reduced to the 0.1% level by creating conditions where asymmetry amplification is much greater.

  20. Evanescent Wave Atomic Mirror

    NASA Astrophysics Data System (ADS)

    Ghezali, S.; Taleb, A.

    2008-09-01

    A research project at the "Laboratoire d'électronique quantique" consists in a theoretical study of the reflection and diffraction phenomena via an atomic mirror. This poster presents the principle of an atomic mirror. Many groups in the world have constructed this type of atom optics experiments such as in Paris-Orsay-Villetaneuse (France), Stanford-Gaithersburg (USA), Munich-Heidelberg (Germany), etc. A laser beam goes into a prism with an incidence bigger than the critical incidence. It undergoes a total reflection on the plane face of the prism and then exits. The transmitted resulting wave out of the prism is evanescent and repulsive as the frequency detuning of the laser beam compared to the atomic transition δ = ωL-ω0 is positive. The cold atomic sample interacts with this evanescent wave and undergoes one or more elastic bounces by passing into backward points in its trajectory because the atoms' kinetic energy (of the order of the μeV) is less than the maximum of the dipolar potential barrier ℏΩ2/Δ where Ω is the Rabi frequency [1]. In fact, the atoms are cooled and captured in a magneto-optical trap placed at a distance of the order of the cm above the prism surface. The dipolar potential with which interact the slow atoms is obtained for a two level atom in a case of a dipolar electric transition (D2 Rubidium transition at a wavelength of 780nm delivered by a Titane-Saphir laser between a fundamental state Jf = l/2 and an excited state Je = 3/2). This potential is corrected by an attractive Van der Waals term which varies as 1/z3 in the Lennard-Jones approximation (typical atomic distance of the order of λ0/2π where λ0 is the laser wavelength) and in 1/z4 if the distance between the atom and its image in the dielectric is big in front of λ0/2π. This last case is obtained in a quantum electrodynamic calculation by taking into account an orthornormal base [2]. We'll examine the role of spontaneous emission for which the rate is inversely

  1. Interaction of wide band gap single crystals with 248 nm excimer laser radiation. XII. The emission of negative atomic ions from alkali halides

    SciTech Connect

    Kimura, Kenichi; Langford, S. C.; Dickinson, J. T.

    2007-12-01

    Many wide band gap materials yield charged and neutral emissions when exposed to sub-band-gap laser radiation at power densities below the threshold for optical breakdown and plume formation. In this work, we report the observation of negative alkali ions from several alkali halides under comparable conditions. We observe no evidence for negative halogen ions, in spite of the high electron affinities of the halogens. Significantly, the positive and negative alkali ions show a high degree of spatial and temporal overlap. A detailed study of all the relevant particle emissions from potassium chloride (KCl) suggests that K{sup -} is formed by the sequential attachment of two electrons to K{sup +}.

  2. Atomic polarizabilities

    SciTech Connect

    Safronova, M. S.; Mitroy, J.; Clark, Charles W.; Kozlov, M. G.

    2015-01-22

    The atomic dipole polarizability governs the first-order response of an atom to an applied electric field. Atomic polarization phenomena impinge upon a number of areas and processes in physics and have been the subject of considerable interest and heightened importance in recent years. In this paper, we will summarize some of the recent applications of atomic polarizability studies. A summary of results for polarizabilities of noble gases, monovalent, and divalent atoms is given. The development of the CI+all-order method that combines configuration interaction and linearized coupled-cluster approaches is discussed.

  3. The Infrared Spectra of Polycyclic Aromatic Hydrocarbons with Excess Peripheral H Atoms (Hn-PAHs) and their Relation to the 3.4 and 6.9 µm PAH Emission Features

    PubMed Central

    Sandford, Scott A.; Bernstein, Max P.; Materese, Christopher K.

    2015-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are likely responsible for the family of infrared emission features seen in a wide variety of astrophysical environments. A potentially important subclass of these materials are PAHs whose edges contain excess H atoms (Hn-PAHs). This type of compound may be present in space, but it has been difficult to assess this possibility because of a lack of suitable laboratory spectra to assist with analysis of astronomical data. We present 4000-500 cm−1 (2.5–20 µm) infrared spectra of 23 Hn-PAHs and related molecules isolated in argon matrices under conditions suitable for interpretation of astronomical data. Spectra of molecules with mixed aromatic and aliphatic domains show characteristics that distinguish them from fully aromatic PAH equivalents. Two major changes occur as PAHs become more hydrogenated: (1) aromatic C-H stretching bands near 3.3 µm weaken and are replaced with stronger aliphatic bands near 3.4 µm, and (2) aromatic C-H out-of-plane bending mode bands in the 11–15 µm region shift and weaken concurrent with growth of a strong aliphatic -CH2-deformation mode near 6.9 µm. Implications for interpreting astronomical spectra are discussed with emphasis on the 3.4 and 6.9 µm features. Laboratory data is compared with emission spectra from IRAS 21282+5050, an object with normal PAH emission features, and IRAS 22272+5435 and IRAS 0496+3429, two protoplanetary nebulae with abnormally large 3.4 µm features. We show that ‘normal’ PAH emission objects contain relatively few Hn-PAHs in their emitter populations, but less evolved protoplanetary nebulae may contain significant abundances of these molecules. PMID:26435553

  4. THE INFRARED SPECTRA OF POLYCYCLIC AROMATIC HYDROCARBONS WITH EXCESS PERIPHERAL H ATOMS (H {sub n} -PAHs) AND THEIR RELATION TO THE 3.4 AND 6.9 {mu}m PAH EMISSION FEATURES

    SciTech Connect

    Sandford, Scott A.; Bernstein, Max P.; Materese, Christopher K.

    2013-03-01

    Polycyclic aromatic hydrocarbons (PAHs) are likely responsible for the family of infrared emission features seen in a wide variety of astrophysical environments. A potentially important subclass of these materials are PAHs whose edges contain excess H atoms (H {sub n} -PAHs). This type of compound may be present in space, but it has been difficult to assess this possibility because of a lack of suitable laboratory spectra to assist with analysis of astronomical data. We present 4000-500 cm{sup -1} (2.5-20 {mu}m) infrared spectra of 23 H {sub n} -PAHs and related molecules isolated in argon matrices under conditions suitable for interpretation of astronomical data. Spectra of molecules with mixed aromatic and aliphatic domains show characteristics that distinguish them from fully aromatic PAH equivalents. Two major changes occur as PAHs become more hydrogenated: (1) aromatic C-H stretching bands near 3.3 {mu}m weaken and are replaced with stronger aliphatic bands near 3.4 {mu}m, and (2) aromatic C-H out-of-plane bending mode bands in the 11-15 {mu}m region shift and weaken concurrent with growth of a strong aliphatic -CH{sub 2}- deformation mode near 6.9 {mu}m. Implications for interpreting astronomical spectra are discussed with emphasis on the 3.4 and 6.9 {mu}m features. Laboratory data is compared with emission spectra from IRAS 21282+5050, an object with normal PAH emission features, and IRAS 22272+5435 and IRAS 0496+3429, two protoplanetary nebulae with abnormally large 3.4 {mu}m features. We show that 'normal' PAH emission objects contain relatively few H {sub n} -PAHs in their emitter populations, but less evolved protoplanetary nebulae may contain significant abundances of these molecules.

  5. The Infrared Spectra of Polycyclic Aromatic Hydrocarbons with Excess Peripheral H Atoms (H(sub n)-PAHs) and their Relation to the 3.4 and 6.9 Micrometer PAH Emission Features

    NASA Technical Reports Server (NTRS)

    Sandford, Scott A.; Bernstein, Max P.; Materese, Christopher K.

    2013-01-01

    A population of polycyclic aromatic hydrocarbons (PAHs) and related materials are thought to be responsible for the family of infrared emission features that are seen towards a wide variety of astrophysical environments. A potentially important subclass of these materials are polycyclic aromatic hydrocarbons whose edges contain excess H atoms (H(sub n)-PAHs). While it has been suggested that this type of compound may be present in the interstellar population, it has been difficult to properly assess this possibility because of a lack of suitable infrared laboratory spectra to assist with analysis of the astronomical data. We present the 4000-500 cm(exp -1) (2.5-20 micrometers) infrared spectra of 23 H(sub n)-PAHs and related molecules isolated in argon matrices, under conditions suitable for use in the interpretation of astronomical data. The spectra of molecules with mixed aromatic and aliphatic domains show unique characteristics that distinguish them from their fully aromatic PAH equivalents. We discuss the changes to the spectra of these types of molecules as they transition from fully aromatic to fully aliphatic forms. The implications for the interpretation of astronomical spectra are discussed with specific emphasis on the 3.4 and 6.9 micrometer features. Laboratory data is compared with emission spectra from IRAS 21282+5050, an object with normal PAH emission features, in addition to IRAS 22272+5435 and IRAS 0496+3429, two protoplanetary nebulae with abnormally large 3.4 micrometer features. We show that 'normal' PAH emission objects contain relatively few H(sub n)-PAHs in their emitter populations, but less evolved protoplanetary nebulae may contain significant abundances of these molecules.

  6. Determination of microamounts of hafnium in zirconium using inductively coupled plasma atomic emission spectrometry and inductively coupled plasma mass spectrometry during their separation by ion exchange on Diphonix chelating resin.

    PubMed

    Smolik, Marek; Jakóbik-Kolon, Agata

    2009-04-01

    Inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICPMS) methods were applied to check the possibility of determination of hafnium in zirconium at a level lower than 100 ppm. A zirconium matrix of hafnium content lower than 10 ppm was obtained using a worked-out separation method exploiting ion exchange on Diphonix resin. Both methods give results in good agreement with each other as well as with those for certified reference material BCR-098 (Zircaloy-4). They were utilized in determination of Hf in the samples collected during separation of microamounts of hafnium from zirconium by the mentioned ion exchange. These results proved the earlier described method of separation on Diphonix resin to be effective even when the initial concentration of hafnium in zirconium decreases from 2.4% to 0.0082%.

  7. Determination of hafnium at the 10(-4)% level (relative to zirconium content) using neutron activation analysis, inductively coupled plasma mass spectrometry and inductively coupled plasma atomic emission spectrometry.

    PubMed

    Smolik, Marek; Polkowska-Motrenko, Halina; Hubicki, Zbigniew; Jakóbik-Kolon, Agata; Danko, Bożena

    2014-01-01

    Hafnium at the very low level of 1-8 ppm (in relation to zirconium) was determined in zirconium sulfate solutions (originating from investigations of the separation of ca. 44 ppm Hf from zirconium by means of the ion exchange method) by using three independent methods: inductively coupled plasma mass spectrometry (ICP MS), neutron activation analysis (NAA) and inductively coupled plasma atomic emission spectrometry (ICP-AES). The results of NAA and ICP MS determinations were consistent with each other across the entire investigated range (the RSD of both methods did not exceed 38%). The results of ICP-AES determination were more diverse, particularly at less than 5 ppm Hf (RSD was significantly higher: 29-253%). The ion exchange method exploiting Diphonix(®) resin proved sufficient efficiency in Zr-Hf separation when the initial concentration ratio of the elements ([Zr]0/[Hf]0) ranged from 1200 to ca. 143,000.

  8. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; determination of dissolved aluminum and boron in water by inductively coupled plasma-atomic emission spectrometry

    USGS Publications Warehouse

    Struzeski, T.M.; DeGiacomo, W.J.; Zayhowski, E.J.

    1996-01-01

    Inductively coupled plasma-atomic emission spectrometry is a sensitive, rapid, and accurate method for determining the dissolved concentration of aluminum and boron in water samples. The method detection limits are 5 micrograms per liter for aluminum and 4 micrograms per liter for boron. For aluminum, low-level (about 30 micrograms per liter) short-term precision (single-operator, seven days) is about 5 percent relative standard deviation and the low-level long-term precision (single-operator, nine months) is about 8 percent relative standard deviation. For boron, the low-level short-term precision is about 4 percent relative standard deviation, and the low-level long-term precision is about 5 percent relative standard deviation. Spike recoveries for aluminum ranged from 86 to 100 percent, and recoveries for boron ranged from 92 to 109 percent.

  9. Acquired acid resistance of human enamel treated with laser (Er:YAG laser and Co2 laser) and acidulated phosphate fluoride treatment: An in vitro atomic emission spectrometry analysis

    PubMed Central

    Mathew, Anju; Reddy, N. Venugopal; Sugumaran, D. K.; Peter, Joby; Shameer, M.; Dauravu, Liju Marcely

    2013-01-01

    Background: Dental caries is essentially a process of diffusion and dissolution. If the aspect of dissolution can be curtailed some degree of prevention can be achieved. Aims: The present study was carried out to evaluate and compare the effect of Er:YAG laser and Co2 laser irradiation combined with acidulated phosphate fluoride treatment on in vitro acid resistance of human enamel. Design: An in vitro study was carried out on 30 human premolars to evaluate the enamel's acid resistance using an atomic emission spectrometry analysis. Materials and Methods: A total of 60 enamel specimens were prepared from 30 human premolars and were randomly assigned to 6 groups: (1) Untreated (control); (2) 1.23% acidulated phosphate fluoride (APF) gel application alone for 4 min; (3) Er:YAG laser treatment alone; (4) Co2 laser treatment alone; (5) Er:YAG laser + APF gel application; (6) Co2 laser + APF gel application. The specimens were then individually immersed in 5 ml of acetate buffer solution (0.1 mol/L, pH 4.5) and incubated at 37°C for 24 h, and the acid resistance was evaluated by determining the calcium ion concentration using the atomic emission spectrometry. Statistical Analysis: An ANOVA model was constructed (P value of 0.05), followed by Tukey's test for multiple pair wise comparisons of mean values. Results: Significant differences were found between the control group and the test groups (P < 0.001). Conclusions: Combining acidulated phosphate fluoride with either Er:YAG or Co2 laser had a synergistic effect in decreasing the enamel demineralization more than either fluoride treatment or laser treatment alone. PMID:24015004

  10. Light propagation through atomic vapours

    NASA Astrophysics Data System (ADS)

    Siddons, Paul

    2014-05-01

    This tutorial presents the theory necessary to model the propagation of light through an atomic vapour. The history of atom-light interaction theories is reviewed, and examples of resulting applications are provided. A numerical model is developed and results presented. Analytic solutions to the theory are found, based on approximations to the numerical work. These solutions are found to be in excellent agreement with experimental measurements.

  11. Direct solid analysis of powdered tungsten carbide hardmetal precursors by laser-induced argon spark ablation with inductively coupled plasma atomic emission spectrometry.

    PubMed

    Holá, Markéta; Kanický, Viktor; Mermet, Jean-Michel; Otruba, Vítezslav

    2003-12-01

    The potential of the laser-induced argon spark atomizer (LINA-Spark atomizer) coupled with ICP-AES as a convenient device for direct analysis of WC/Co powdered precursors of sintered hardmetals was studied. The samples were presented for the ablation as pressed pellets prepared by mixing with powdered silver binder containing GeO2 as internal standard. The pellets were ablated with the aid of a Q-switched Nd:YAG laser (1064 nm) focused 16 mm behind the target surface with a resulting estimated power density of 5 GW cm(-2). Laser ablation ICP-AES signals were studied as a function of ablation time, and the duration of time prior to measurement (pre-ablation time) which was necessary to obtain reliable results was about 40 s. Linear calibration plots were obtained up to 10% (m/m) Ti, 9% Ta and 3.5% Nb both without internal standardization and by using germanium as an added internal standard or tungsten as a contained internal standard. The relative uncertainty at the centroid of the calibration line was in the range from +/- 6% to +/- 11% for Nb, Ta and Ti both with and without internal standardisation by Ge. A higher spread of points about the regression was observed for cobalt for which the relative uncertainty at the centroid was in the range from +/- 9% to +/- 14%. Repeatability of results was improved by the use of both Ge and W internal standards. The lowest determinable quantities calculated for calibration plots were 0.060% Co, 0.010% Nb, 0.16% Ta and 0.030% Ti with internal standardization by Ge. The LA-ICP-AES analyses of real samples led to good agreement with the results obtained by solution-based ICP determination with a relative bias not exceeding 10%. The elimination of the dissolution procedure of powdered tungsten (Nb, Ta, Ti) carbide is the principal advantage of the developed LA-ICP-AES method.

  12. Analytical model of Europa's O2 exosphere

    NASA Astrophysics Data System (ADS)

    Milillo, Anna; Plainaki, Christina; Orsini, Stefano; Mangano, Valeria; Massetti, Stefano; Mura, Alessandro

    2014-05-01

    The origin of the exosphere of Europa is its water ice surface. The existing exosphere models, assuming either a collisionless environment (simple Monte Carlo techniques) or a kinetic approach (Direct Monte Carlo Method) both predicts that the major constituent of the exosphere is molecular oxygen. Specifically, O2 is generated at the surface through radiolysis and chemical interactions of the water dissociation products. The non-escaping O2 molecules circulate around the moon impacting the surface several times, due to their long lifetime and due to their non-sticking, suffering thermalization to the surface temperature after each impact. In fact, the HST observations of the O emission lines have manifested the presence of an asymmetric atomic Oxygen envelope, evidencing the existence of a thin asymmetric molecular Oxygen atmosphere. The existing Monte Carlo models are not easily applicable as input of simulations devoted to the study of the plasma interactions with the moon. On the contrary, it would be important to have a suitable and user-friendly model to use as a tool. This study presents an analytical 3D model that is able to describe the molecular Oxygen exosphere by reproducing the asymmetries due to different configurations among Europa, Jupiter and the Sun. This model is obtained by a non-linear fit procedure of the EGEON Monte Carlo model results to a Chamberlain density profile. Different parameters of the model are able to describe various exosphere properties thus allowing a detailed investigation of the exospheric characteristics.

  13. Superradiant Pulse And Amplified Spontaneous Emission From The Flash Pumped Atomic Iodine System Undergoing The Laser Transition Of 2P 1/2- 2P3/2

    NASA Astrophysics Data System (ADS)

    Hahn, Jae W.; Kim, Gyu U.; Lee, Sang S.

    1987-01-01

    Recently, Jaroszynski and King found superradiance(SR) occurring in photodissociatively created systems using NaI and n-C3F7I moleculesl) , and Hahn and Lee have performe2)d the amplified spontaneous emission(ASE) experiment in an iodine photodissociation laser(IPL) amplifier . In general, to observe SR experimentally, a very short intense pumping pulse of which FWHM is about a few tens of nanoseconds, is used for making a totally inverted system. But in this work, the amplifier is pumped with conventional flashlamps of FWHM=3us, yet we have detected a output pulse which is a superposition of ASE and SR. The temporal behaviour of the pulse is investigated in detail, and the experimental results are compared with theoretical results.

  14. Determination of metal content in valerian root phytopharmaceutical derivatives by atomic spectrometry.

    PubMed

    Arce, Silvia; Cerutti, Soledad; Olsina, Roberto; Gomez, María R; Martínez, Luis D

    2005-01-01

    Phytopharmaceuticals containing Valerian are used as mild sleep-inducing agents. The elemental composition of 3 different marks of Valeriana officinalis roots commercially available in the Argentinian market, their teas, and a commercial tincture have been studied. The content of Al, Ca, Cd, Co, Cr, Cu, Fe, Li, Mn, Ni, Pb, V, and Zn was determined in phytopharmaceuticals by flame atomic emission/absorption spectrometry, electrothermal atomic absorption spectrometry, and ultrasonic nebulization coupled to inductively coupled plasma-optical emission spectrometry. Prior to analyses of the samples, a digestion procedure was optimized. The analytical results obtained for Fe, Al, Ca, and V in the solid sample study were within the range 100-1000 mg/kg, and for Mn, Zn, and Pb within the range 10-100 mg/kg. Cadmium was found at levels up to 0.0125 mg/kg. PMID:15759744

  15. Phase-matched emission from an optically thin medium following one-photon pulse excitation: Energy considerations

    SciTech Connect

    Berman, P. R.; Le Goueet, J.-L.

    2011-03-15

    Scully and coworkers [M. O. Scully, E. S. Fry, C. H. R. Oii, and K. Wodkiewicz, Phys. Rev. Lett. 96, 010501 (2006)] demonstrated that there is directional, phase-matched emission following the excitation of an ensemble of atoms by a single-photon pulse. While the phase-matched emission intensity is proportional to the the number of atoms, for optically thin samples the total energy emitted in the phase-matched direction is much less than that radiated in other directions. Moreover, even for optically thin samples, it is necessary to take into account effects related to cooperative decay if energy is to be conserved in the overall emission process. An analytic calculation is presented to show explicitly how cooperative decay reduces the incoherent emission and restores energy conservation in this low-density limit.

  16. O-atom degradation mechanisms of materials

    NASA Technical Reports Server (NTRS)

    Coulter, Daniel R.; Liang, Ranty H.; Chung, Shirley Y.; Smith, Keri Oda; Gupta, Amitava

    1987-01-01

    The low Earth orbit environment is described and the critical issues relating to oxygen atom degradation are discussed. Some analytic techniques for studying the problem and preliminary results on the underlying degradation mechanisms are presented.

  17. Atomic supersymmetry

    NASA Technical Reports Server (NTRS)

    Kostelecky, V. Alan

    1993-01-01

    Atomic supersymmetry is a quantum-mechanical supersymmetry connecting the properties of different atoms and ions. A short description of some established results in the subject are provided and a few recent developments are discussed including the extension to parabolic coordinates and the calculation of Stark maps using supersymmetry-based models.

  18. Atomic Calligraphy

    NASA Astrophysics Data System (ADS)

    Imboden, Matthias; Pardo, Flavio; Bolle, Cristian; Han, Han; Tareen, Ammar; Chang, Jackson; Christopher, Jason; Corman, Benjamin; Bishop, David

    2013-03-01

    Here we present a MEMS based method to fabricate devices with a small number of atoms. In standard semiconductor fabrication, a large amount of material is deposited, after which etching removes what is not wanted. This technique breaks down for structures that approach the single atom limit, as it is inconceivable to etch away all but one atom. What is needed is a bottom up method with single or near single atom precision. We demonstrate a MEMS device that enables nanometer position controlled deposition of gold atoms. A digitally driven plate is swept as a flux of gold atoms passes through an aperture. Appling voltages on four comb capacitors connected to the central plate by tethers enable nanometer lateral precision in the xy plane over 15x15 sq. microns. Typical MEMS structures have manufacturing resolutions on the order of a micron. Using a FIB it is possible to mill apertures as small as 10 nm in diameter. Assuming a low incident atomic flux, as well as an integrated MEMS based shutter with microsecond response time, it becomes possible to deposit single atoms. Due to their small size and low power consumption, such nano-printers can be mounted directly in a cryogenic system at ultrahigh vacuum to deposit clean quench condensed metallic structures.

  19. ARPEFS as an analytic technique

    SciTech Connect

    Schach von Wittenau, A.E.

    1991-04-01

    Two modifications to the ARPEFS technique are introduced. These are studied using p(2 {times} 2)S/Cu(001) as a model system. The first modification is the obtaining of ARPEFS {chi}(k) curves at temperatures as low as our equipment will permit. While adding to the difficulty of the experiment, this modification is shown to almost double the signal-to-noise ratio of normal emission p(2 {times} 2)S/Cu(001) {chi}(k) curves. This is shown by visual comparison of the raw data and by the improved precision of the extracted structural parameters. The second change is the replacement of manual fitting of the Fourier filtered {chi}(k) curves by the use of the simplex algorithm for parameter determination. Again using p(2 {times} 2)S/Cu(001) data, this is shown to result in better agreement between experimental {chi}(k) curves and curves calculated based on model structures. The improved ARPEFS is then applied to p(2 {times} 2)S/Ni(111) and ({radical}3 {times} {radical}3) R30{degree}S/Ni(111). For p(2 {times} 2)S/Cu(001) we find a S-Cu bond length of 2.26 {Angstrom}, with the S adatom 1.31 {Angstrom} above the fourfold hollow site. The second Cu layer appears to be corrugated. Analysis of the p(2 {times} 2)S/Ni(111) data indicates that the S adatom adatom adsorbs onto the FCC threefold hollow site 1.53 {Angstrom} above the Ni surface. The S-Ni bond length is determined to be 2.13 {Angstrom}, indicating an outwards shift of the first layer Ni atoms. We are unable to assign a unique structure to ({radical}3 {times} {radical}3)R30{degree}S/Ni(111). An analysis of the strengths and weaknesses of ARPEFS as an experimental and analytic technique is presented, along with a summary of problems still to be addressed.

  20. Quantum Amplification by Superradiant Emission of Radiation

    NASA Astrophysics Data System (ADS)

    Svidzinsky, Anatoly A.; Yuan, Luqi; Scully, Marlan O.

    2013-10-01

    A laser generates light through stimulated emission of radiation and requires population inversion. Quantum interference can yield lasing without inversion. However, such phase-sensitive quantum amplification still requires some atomic population in the excited state. Here, we present a new kind of quantum amplifier based on collective superradiant emission which does not need any population in the excited state. We show that parametric resonance between the driving (e.g., infrared) field and collective superradiant oscillations of the atomic polarization can yield light amplification at high (e.g., XUV) frequencies. To achieve gain, one must suppress a time-dependent Stark shift caused by the driving field. The resulting superradiant amplifier is many orders of magnitude more efficient than the usual nonlinear multiphoton excitation and holds promise for a new kind of generator of high-frequency coherent radiation. In addition to a detailed analytical analysis, confirmed by numerical simulations, we provide a physically appealing explanation of the quantum amplification by superradiant emission of radiation (QASER) operation in terms of coupled classical oscillators. We also present an experiment that demonstrates the QASER amplification mechanism in an electronic circuit, which, to the best of our knowledge, is the first experimental demonstration of the difference combination resonance.

  1. Laser-excited atomic fluorescence spectrometry in a pressure-controlled electrothermal atomizer.

    PubMed

    Lonardo, R F; Yuzefovsky, A I; Irwin, R L; Michel, R G

    1996-02-01

    A theoretical model was developed to describe the loss of analyte atoms in graphite furnaces during atomization. The model was based on two functions, one that described the supply of analyte by vaporization, and another that described the removal of the analyte by diffusion. Variation in working pressure was shown to affect the competition between these two processes. Optimal atomization efficiency was predicted to occur at a pressure where the supply of the analyte was maximized, and gas phase interactions between the analyte and matrix were minimized. Experiments to test the model included the direct determination of phosphorus and tellurium in nickel alloys and of cobalt in glass. In all cases, reduction in working pressure from atmospheric pressure to 7 Pa decreased sensitivity by 2 orders of magnitude, but improved temporal peak shape. For the atomization of tellurium directly from a solid nickel alloy, and the atomization of cobalt from an aqueous solution, no change in sensitivity was observed as the working pressure was reduced from atmospheric pressure to approximately 70 kPa. If a reduction in working pressure affected only the diffusion of the analyte, poorer sensitivity should have been obtained. Only a commensurate increase in analyte vaporization could account for maintained sensitivity at lower working pressures. Overall, analyte vaporization was not dramatically improved at reduced working pressures, and maximum atomization efficiency was found to occur near atmospheric pressure. PMID:8712359

  2. Study of surface reaction of spinel Li4Ti5O12 during the first lithium insertion and extraction processes using atomic force microscopy and analytical transmission electron microscopy.

    PubMed

    Kitta, Mitsunori; Akita, Tomoki; Maeda, Yasushi; Kohyama, Masanori

    2012-08-21

    Spinel lithium titanate (Li(4)Ti(5)O(12), LTO) is a promising anode material for a lithium ion battery because of its excellent properties such as high rate charge-discharge capability and life cycle stability, which were understood from the viewpoint of bulk properties such as small lattice volume changes by lithium insertion. However, the detailed surface reaction of lithium insertion and extraction has not yet been studied despite its importance to understand the mechanism of an electrochemical reaction. In this paper, we apply both atomic force microscopy (AFM) and transmission electron microscopy (TEM) to investigate the changes in the atomic and electronic structures of the Li(4)Ti(5)O(12) surface during the charge-discharged (lithium insertion and extraction) processes. The AFM observation revealed that irreversible structural changes of an atomically flat Li(4)Ti(5)O(12) surface occurs at the early stage of the first lithium insertion process, which induces the reduction of charge transfer resistance at the electrolyte/Li(4)Ti(5)O(12) interface. The TEM observation clarified that cubic rock-salt crystal layers with a half lattice size of the original spinel structure are epitaxially formed after the first charge-discharge cycle. Electron energy loss spectroscopy (EELS) observation revealed that the formed surface layer should be α-Li(2)TiO(3). Although the transformation of Li(4)Ti(5)O(12) to Li(7)Ti(5)O(12) is well-known as the lithium insertion reaction of the bulk phase, the generation of surface product layers should be inevitable in real charge-discharge processes and may play an effective role in the stable electrode performance as a solid-electrolyte interphase (SEI).

  3. Simplified Analytical Solution for Martian OH*-layer Altitude

    NASA Astrophysics Data System (ADS)

    Grygalashvyly, Mykhaylo; Sonnemann, Gerd

    2016-04-01

    In the Earth atmosphere airglow emissions of OH* are used in very diverse branches of research from gravity waves (GWs) and tides observations to minor chemical constituents and temperature measurements. Moreover, the airglow observations have good potential as, for example, for water vapor profile retrieval in the mesopause region. Recently, hydroxyl emissions were found in Mars and in Venus atmospheres. Thus, the applicability potential has been increased in spurts. Even for Earth's atmosphere there is a lack of knowledge on morphology of OH*-layer, i.e. on altitude, number density and shape variability with the intro- and extra-annual cycles, due to planetary waves (PWs), GWs, and tides. The questions on relations between OH* layer altitude, number density (volume emission, intensity), surrounding temperature, and winds (meridional and vertical) are still open. Modern satellite airglow measurements are not enough precise with a typical error in determination of altitude ~2-3 km, while the ground-based measurements are restricted by local point of observations and integrated volume emission. Thus, retrievals of emission altitudes variations to derive are awkward. The difficulties are much stronger for the investigation of the Martian OH*-layer variability and altitude diagnostics. We introduce a simplified analytical approach for OH*-layer altitude in the Martian atmosphere. The expressions for the number density and height of the OH*-layer peak, as well as relationship between both parameters, are derived for night time conditions. These OH*-layer parameters are determined by the temperature, atomic oxygen density and their vertical gradients. The approximations can be useful for analysis of ground-based and satellite-borne airglow observations. We discuss the consequences following from the derived expression.

  4. Atom-interferometric studies of light scattering

    SciTech Connect

    Beattie, S.; Barrett, B.; Chan, I.; Mok, C.; Kumarakrishnan, A.; Yavin, I.

    2009-07-15

    We have used an echo-type atom interferometer that manipulates laser-cooled atoms in a single ground state to investigate the effect of light scattering from pulsed and continuous-wave light. The interferometer uses two off-resonant standing-wave pulses applied at times t=0 and t=T to diffract and recombine momentum states separated by 2({Dirac_h}/2{pi})k at t=2T. Matter wave interference is associated with the formation of a density grating with period {lambda}/2 in the vicinity of this echo time. The grating contrast is measured by recording the intensity of coherently backscattered light. The interferometer is perturbed by an additional pulse applied at t=2T-{delta}T or by continuous-wave background light. If the additional pulse is a standing wave, the momentum states interfering at t=2T are displaced and the grating contrast can be completely recovered due to constructive interference. In this case, the contrast shows a periodic modulation at the atomic recoil frequency as a function of {delta}T. In a recent work, it was shown that the atomic recoil frequency can be measured easily and precisely when using coherence functions to model the signal shape. This paper provides an alternative description of the signal shape through an analytical calculation of echo formation in the presence of an additional standing-wave pulse. Using this treatment, it is possible to model the effects of spontaneous emission and spatial profile of the laser beam on the signal shape. Additionally, the theory predicts scaling laws as a function of the pulse area and the number of additional standing-wave pulses. These scaling laws are investigated experimentally and can be exploited to improve precision measurements of the atomic recoil frequency. We also show that coherence functions can be used to make a direct measurement of the populations of momentum states associated with the ground state under conditions where the Doppler-broadened velocity distribution of the sample is much

  5. CORONAL EMISSION LINES AS THERMOMETERS

    SciTech Connect

    Judge, Philip G.

    2010-01-10

    Coronal emission-line intensities are commonly used to measure electron temperatures using emission measure and/or line ratio methods. In the presence of systematic errors in atomic excitation calculations and data noise, the information on underlying temperature distributions is fundamentally limited. Increasing the number of emission lines used does not necessarily improve the ability to discriminate between different kinds of temperature distributions.

  6. Ab initio analytical Raman intensities for periodic systems through a coupled perturbed Hartree-Fock/Kohn-Sham method in an atomic orbital basis. II. Validation and comparison with experiments

    NASA Astrophysics Data System (ADS)

    Maschio, Lorenzo; Kirtman, Bernard; Rérat, Michel; Orlando, Roberto; Dovesi, Roberto

    2013-10-01

    In this work, we validate a new, fully analytical method for calculating Raman intensities of periodic systems, developed and presented in Paper I [L. Maschio, B. Kirtman, M. Rérat, R. Orlando, and R. Dovesi, J. Chem. Phys. 139, 164101 (2013)]. Our validation of this method and its implementation in the CRYSTAL code is done through several internal checks as well as comparison with experiment. The internal checks include consistency of results when increasing the number of periodic directions (from 0D to 1D, 2D, 3D), comparison with numerical differentiation, and a test of the sum rule for derivatives of the polarizability tensor. The choice of basis set as well as the Hamiltonian is also studied. Simulated Raman spectra of α-quartz and of the UiO-66 Metal-Organic Framework are compared with the experimental data.

  7. Kinetic Atom.

    ERIC Educational Resources Information Center

    Wilson, David B.

    1981-01-01

    Surveys the research of scientists like Joule, Kelvin, Maxwell, Clausius, and Boltzmann as it comments on the basic conceptual issues involved in the development of a more precise kinetic theory and the idea of a kinetic atom. (Author/SK)

  8. Acting Atoms.

    ERIC Educational Resources Information Center

    Farin, Susan Archie

    1997-01-01

    Describes a fun game in which students act as electrons, protons, and neutrons. This activity is designed to help students develop a concrete understanding of the abstract concept of atomic structure. (DKM)

  9. Analytic study of the chain dark decomposition reaction of iodides - atomic iodine donors - in the active medium of a pulsed chemical oxygen-iodine laser: 1. Criteria for the development of the branching chain dark decomposition reaction of iodides

    SciTech Connect

    Andreeva, Tamara L; Kuznetsova, S V; Maslov, Aleksandr I; Sorokin, Vadim N

    2009-02-28

    The scheme of chemical processes proceeding in the active medium of a pulsed chemical oxygen-iodine laser (COIL) is analysed. Based on the analysis performed, the complete system of differential equations corresponding to this scheme is replaced by a simplified system of equations describing in dimensionless variables the chain dark decomposition of iodides - atomic iodine donors, in the COIL active medium. The procedure solving this system is described, the basic parameters determining the development of the chain reaction are found and its specific time intervals are determined. The initial stage of the reaction is analysed and criteria for the development of the branching chain decomposition reaction of iodide in the COIL active medium are determined. (active media)

  10. Analytics for Education

    ERIC Educational Resources Information Center

    MacNeill, Sheila; Campbell, Lorna M.; Hawksey, Martin

    2014-01-01

    This article presents an overview of the development and use of analytics in the context of education. Using Buckingham Shum's three levels of analytics, the authors present a critical analysis of current developments in the domain of learning analytics, and contrast the potential value of analytics research and development with real world…

  11. Let's Talk... Analytics

    ERIC Educational Resources Information Center

    Oblinger, Diana G.

    2012-01-01

    Talk about analytics seems to be everywhere. Everyone is talking about analytics. Yet even with all the talk, many in higher education have questions about--and objections to--using analytics in colleges and universities. In this article, the author explores the use of analytics in, and all around, higher education. (Contains 1 note.)

  12. Acoustic emission descriptors

    NASA Astrophysics Data System (ADS)

    Witos, Franciszek; Malecki, Ignacy

    The authors present selected problems associated with acoustic emission interpreted as a physical phenomenon and as a measurement technique. The authors examine point sources of acoustic emission in isotropic, homogeneous linearly elastic media of different shapes. In the case of an unbounded medium the authors give the analytical form of the stress field and the wave shift field of the acoustic emission. In the case of a medium which is unbounded plate the authors give a form for the equations which is suitable for numerical calculation of the changes over time of selected acoustic emission values. For acoustic emission as a measurement technique, the authors represent the output signal as the resultant of a mechanical input value which describes the source, the transient function of the medium, and the transient function of specific components of the measurement loop. As an effect of this notation, the authors introduce the distinction between an acoustic measurement signal and an acoustic measurement impulse. The authors define the basic parameters of an arbitrary impulse. The authors extensively discuss the signal functions of acoustic emission impulses and acoustic emission signals defined in this article as acoustic emission descriptors (or signal functions of acoustic emission impulses) and advanced acoustic emission descriptors (which are either descriptors associated with acoustic emission applications or the signal functions of acoustic emission signals). The article also contains the results of experimental research on three different problems in which acoustic emission descriptors associated with acoustic emission pulses, acoustic emission applications, and acoustic emission signals are used. These problems are respectively: a problem of the amplitude-load characteristics of acoustic emission pulses in carbon samples subjected to compound uniaxial compression, the use of acoustic emission to predict the durability characteristics of conveyor belts, and

  13. Detection of palladium by cold atom solution atomic absorption.

    PubMed

    Molloy, John L; Holcombe, James A

    2006-09-15

    One of the largest obstacles in miniaturizing traditional atomic spectroscopic sources is the need for a thermal/electrical source for free atom production. A single article in the literature has demonstrated atomic absorption detection of Ag, Cu, and Pd in solution at room temperature for atoms in the gas phase, which may ultimately permit miniaturization. Unfortunately, several laboratories have found that reproducing the phenomenon has been difficult. Without a sound fundamental explanation of the processes leading to the signal, one must conclude that it can be done, but some unsuspected and unknown design/methodological nuances are responsible for only a single reported success. Gas phase atoms could exist at room temperature "in solution" if the atoms were trapped in very small bubbles. In the current study, submicrometer-sized bubbles were created in a flow-through cell during the mixing of an alcohol-water solution containing a reducing agent with water containing the analyte. A repeatable atomic absorption signal was produced. Replacement of ethanol with 1-propanol and use of a surfactant increased the signal. Limits of detection of approximately 100 ppb in Pd were achieved, and it is estimated that approximately 0.4% of the Pd initially added is contained within the bubbles as gaseous atoms. The paper discusses the fundamental processes needed to achieve a repeatable signal. PMID:16970344

  14. Atomic oxygen exposure of LDEF experiment trays

    NASA Technical Reports Server (NTRS)

    Bourassa, R. J.; Gillis, J. R.

    1992-01-01

    Atomic oxygen exposures were determined analytically for rows, longerons, and end bays of the Long Duration Exposure Facility (LDEF). The calculations are based on an analytical model that accounts for the effects of thermal molecular velocity, atmospheric temperature, number density, spacecraft velocity, incidence angle, and atmospheric rotation on atomic oxygen flux. Results incorporate variations in solar activity, geomagnetic index, and orbital parameters occurring over the 6-year flight of the spacecraft. To facilitate use of the data, both detailed tabulations and summary charts for atomic oxygen fluences are presented.

  15. Analytical Morse/long-Range model potential and predicted infrared and microwave spectra for a symmetric top-atom dimer: A case study of CH{sub 3}F–He

    SciTech Connect

    Ma, Yong-Tao; Li, Hui; Zeng, Tao

    2014-06-07

    Four-dimensional ab initio intermolecular potential energy surfaces (PESs) for CH{sub 3}F–He that explicitly incorporates dependence on the Q{sub 3} stretching normal mode of the CH{sub 3}F molecule and are parametrically dependent on the other averaged intramolecular coordinates have been calculated. Analytical three-dimensional PESs for v{sub 3}(CH{sub 3}F) = 0 and 1 are obtained by least-squares fitting the vibrationally averaged potentials to the Morse/Long-Range potential function form. With the 3D PESs, we employ Lanczos algorithm to calculate rovibrational levels of the dimer system. Following some re-assignments, the predicted transition frequencies are in good agreement with experimental microwave data for ortho-CH{sub 3}F, with the root-mean-square deviation of 0.042 cm{sup −1}. We then provide the first prediction of the infrared and microwave spectra for the para-CH{sub 3}F–He dimer. The calculated infrared band origin shifts associated with the ν{sub 3} fundamental of CH{sub 3}F are 0.039 and 0.069 cm{sup −1} for para-CH{sub 3}F–He and ortho-CH{sub 3}F–He, respectively.

  16. Element analysis and characteristic identification of non-fumigated and sulfur-fumigated Fritillaria thunbergii Miq. using microwave digestion-inductively coupled plasma atomic emission spectrometry combined with Fourier transform infrared spectrometry

    PubMed Central

    Lou, Yajing; Cai, Hao; Liu, Xiao; Tu, Sicong; Pei, Ke; Zhao, Yingying; Cao, Gang; Li, Songlin; Qin, Kunming; Cai, Baochang

    2014-01-01

    Background: Sulfur-fumigation may induce chemical transformation of traditional Chinese medicines leading to harmful effects following patient ingestion. For quality control, it is urgently needed to develop a reliable and efficient method for sulfur-fumigation identification. Materials and Methods: The spectrochemical identification of non-fumigated and sulfur-fumigated Fritillaria thunbergii Miq. was carried out to evaluate inorganic elements and organic components. The concentrations of 12 elements, including Zn, Mn, Cu, Fe, Li, Mg, Sr, Pb, As, Cd, Hg, and S of samples were determined by microwave digestion - inductively coupled plasma atomic emission spectrometry (ICP-AES). Meanwhile, Fourier transform infrared spectrometry (FTIR) was used for the study of chemical group characteristic reactions after sulfur-fumigation. Results: The concentrations of Fe, Mg, Hg, and S elements showed significant differences between non-fumigated and sulfur-fumigated Fritillaria thunbergii Miq. The characteristic stretching vibrations of some groups in FTIR spectra, such as -OH, -S = O and -S-O, provided the identification basis for the discrimination of non-fumigated and sulfur-fumigated Fritillaria thunbergii Miq. Conclusion: The application of microwave digestion - ICP-AES was successfully used in combination with FTIR to authenticate and evaluate the quality of medicinal Fritillaria thunbergii Miq. Further applications of this technique should be explored. PMID:24914306

  17. Determination of butyl- and phenyltin compounds in human urine by HS-SPME after derivatization with tetraethylborate and subsequent determination by capillary GC with microwave-induced plasma atomic emission and mass spectrometric detection.

    PubMed

    Zachariadis, G A; Rosenberg, E

    2009-04-30

    A headspace solid-phase micro-extraction (HS-SPME) method was developed and optimized for gas chromatographic separation and determination of commonly found organotin compounds in human urine after potential exposure. Butyl- and phenyltin compounds were in situ derivatized to ethylated derivatives by sodium tetraethylborate (NaBEt(4)) directly in the urine matrix. The relevant parameters affecting the yield of the SPME procedure were examined using tetrabutyltin as internal standard. The method was optimized for direct use in the analysis of undiluted human urine samples and mono-, di- and tri-substituted butyl- and phenyltin compounds could be determined after a 15-min headspace extraction time at room temperature. The selectivity of the microwave-induced plasma atomic emission detector (MIP-AED) as an element specific detector in combination with the relatively selective sample preparation technique of HS-SPME allowed the interference-free detection of the organotin compounds in all cases. A quadrupole mass spectrometer was used in parallel experiments as a detector for the confirmation of the identity molecular structure of the eluted compounds. The performance characteristics of the developed method are given for the determination of mixtures of these compounds. Finally the proposed method was applied to the analysis of several human urine samples. PMID:19203626

  18. Determination of methylmercury and butyltin compounds in marine biota and sediments using microwave-assisted acid extraction, solid-phase microextraction, and gas chromatography with microwave-induced plasma atomic emission spectrometric detection.

    PubMed

    Tutschku, Silke; Schantz, Michele M; Wise, Stephen A

    2002-09-15

    A method is described for the determination of methylmercury and butyltin compounds in marine sediment and tissue using microwave-assisted acid extraction or digestion and solid-phase microextraction (SPME) followed by analysis using gas chromatography with microwave-induced plasma atomic emission spectrometric detection (GC-MIP-AES). Using the SPME-GC-MIP-AES method, enrichment factors for methylmercury and butyltin compounds of 50-100 were achieved, as compared to the typical hexane extraction, and measurements in marine tissue and sediment matrixes were possible at 1-2 microg/kg (methylmercury) and 10-100 ng/kg (butyltins). The SPME-GC-MIP-AES method was validated using several marine sediment and tissue matrix certified reference materials (CRMs) with certified values for methylmercury and butyltin compounds. The SPME-GC-MIP-AES method was used to measure methylmercury in four marine tissue CRMs ranging from oyster tissue at 13.0 +/- 1.0 microg/kg to fish tissue at 397 +/- 13 microg/kg (as Hg dry mass). Results from the SPME-GC-MIP-AES method were used in conjunction with results from other techniques to assign certified values for methylmercury in oyster, mussel, and fish tissue CRMs. Mono-, di-, and tributyltin were measured in three sediment CRMs at concentration levels of (0.08 +/- 0.03)-(0.35 +/- 0.05) mg/kg (as Sn dry mass). PMID:12349972

  19. Determination of soluble toxic arsenic species in alga samples by microwave-assisted extraction and high performance liquid chromatography-hydride generation-inductively coupled plasma-atomic emission spectrometry.

    PubMed

    García Salgado, S; Quijano Nieto, M A; Bonilla Simón, M M

    2006-09-29

    A microwave-based procedure for arsenic species extraction in alga samples (Sargassum fulvellum, Chlorella vulgaris, Hizikia fusiformis and Laminaria digitata) is described. Extraction time and temperature were tested in order to evaluate the extraction efficiency of the process. Arsenic compounds were extracted in 8 ml of deionised water at 90 degrees C for 5 min. The process was repeated three times. Soluble arsenic compounds extracted accounted for about 78-98% of total arsenic. The results were compared with those obtained in a previous work, where the extraction process was carried out by ultrasonic focussed probe for 30 s. Speciation studies were carried out by high performance liquid chromatography-hydride generation-inductively coupled plasma-atomic emission spectrometry (HPLC-HG-ICP-AES). The chromatographic method allowed us to separate As(III), As(V), monomethylarsonic acid and dimethylarsinic acid in less than 13 min. The chromatographic analysis of the samples allowed us to identify and quantify As(V) in Hizikia sample and Sargasso material, while the four arsenic species studied were found in Chlorella sample. In the case of Laminaria sample, none of these species was identified by HPLC-HG-ICP-AES. However, in the chromatographic analysis of this alga by HPLC-ICP-AES, an unknown arsenic species was detected.

  20. Determination of soluble toxic arsenic species in alga samples by microwave-assisted extraction and high performance liquid chromatography-hydride generation-inductively coupled plasma-atomic emission spectrometry.

    PubMed

    García Salgado, S; Quijano Nieto, M A; Bonilla Simón, M M

    2006-09-29

    A microwave-based procedure for arsenic species extraction in alga samples (Sargassum fulvellum, Chlorella vulgaris, Hizikia fusiformis and Laminaria digitata) is described. Extraction time and temperature were tested in order to evaluate the extraction efficiency of the process. Arsenic compounds were extracted in 8 ml of deionised water at 90 degrees C for 5 min. The process was repeated three times. Soluble arsenic compounds extracted accounted for about 78-98% of total arsenic. The results were compared with those obtained in a previous work, where the extraction process was carried out by ultrasonic focussed probe for 30 s. Speciation studies were carried out by high performance liquid chromatography-hydride generation-inductively coupled plasma-atomic emission spectrometry (HPLC-HG-ICP-AES). The chromatographic method allowed us to separate As(III), As(V), monomethylarsonic acid and dimethylarsinic acid in less than 13 min. The chromatographic analysis of the samples allowed us to identify and quantify As(V) in Hizikia sample and Sargasso material, while the four arsenic species studied were found in Chlorella sample. In the case of Laminaria sample, none of these species was identified by HPLC-HG-ICP-AES. However, in the chromatographic analysis of this alga by HPLC-ICP-AES, an unknown arsenic species was detected. PMID:16876177