WorldWideScience

Sample records for absorption spectroscopy establishes

  1. Zeeman atomic absorption spectroscopy

    A new method of background correction in atomic absorption spectroscopy has recently been introduced, based on the Zeeman splitting of spectral lines in a magnetic field. A theoretical analysis of the background correction capability observed in such instruments is presented. A Zeeman atomic absorption spectrometer utilizing a 50 Hz sine wave modulated magnetic field is described. (Auth.)

  2. X-ray Absorption Spectroscopy

    Yano, Junko; Yachandra, Vittal K.

    2009-07-09

    This review gives a brief description of the theory and application of X-ray absorption spectroscopy, both X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS), especially, pertaining to photosynthesis. The advantages and limitations of the methods are discussed. Recent advances in extended EXAFS and polarized EXAFS using oriented membranes and single crystals are explained. Developments in theory in understanding the XANES spectra are described. The application of X-ray absorption spectroscopy to the study of the Mn4Ca cluster in Photosystem II is presented.

  3. Graphene intracavity spaser absorption spectroscopy

    Lozovik, Yu. E.; Nechepurenko, I. A.; Dorofeenko, A. V.

    2016-09-01

    We propose an intracavity plasmon absorption spectroscopy method based on graphene active plasmonics. It is shown that the plasmonic cavity contribution to the sensitivity is proportional to the quality factor Q of the graphene plasmonic cavity and reaches two orders of magnitude. The addition of gain medium into the cavity increases the sensitivity of method. Maximum sensitivity is reached in the vicinity of the plasmon generation threshold. The gain contribution to the sensitivity is proportional to Q1/2. The giant amplification of sensitivity in the graphene plasmon generator is associated with a huge path length, limited only by the decoherence processes. An analytical estimation of the sensitivity to loss caused by analyzed particles (molecules, nanoparticles, etc.) normalized by the single pass plasmon scheme is derived. Usage of graphene nanoflakes as plasmonic cavity allows a high spatial resolution to be reached, in addition to high sensitivity.

  4. UV/VUV high sensitivity absorption spectroscopy

    High sensitivity absorption spectroscopy is a powerful diagnostic technique for reactive glow discharges plasmas. Absolute column densities of many chemical radicals have been measured in both deposition and etching plasmas. Modern photodiode or charge-coupled device (CCD) detector arrays vastly increase the sensitivity of traditional absorption experiments enabling one to observe fractional absorptions of ultraviolet (UV) and vacuum ultraviolet (VUV) radiation less than 0.0001. Stable arc lamps provide a continuum source in some experiments, but experiments at very high spectral resolution or at VUV wavelengths require the greater spectral radiance of synchrotron radiation. High sensitivity absorption spectroscopy has been applied to intense glow discharges used for lighting, for diamond film deposition, and for both depositing and etching Si films. Absorption spectroscopy provides absolute column densities, is useful for transitions that do not fluoresce, and approaches the sensitivity of laser-induced fluorescence (LIF) in glow discharges under some conditions

  5. Determination of trace amounts of scandium by atomic absorption spectroscopy.

    Chau, Y K

    1968-05-01

    Optimum instrumental conditions were investigated for the determination of trace quantities of scandium by atomic-absorption spectroscopy. Enhancement effects by organic solvents and by complex extractions were also studied. (46)Sc was used to establish the optimum extraction conditions. A sensitivity of 0.06 ppm of Sc was observed when using extraction into oxine-butanol and atomic absorption was measured with an acetylene-nitrous oxide flame. PMID:18960315

  6. Further advancement of differential optical absorption spectroscopy: theory of orthogonal optical absorption spectroscopy.

    Liudchik, Alexander M

    2014-08-10

    A modified version of the differential optical absorption spectroscopy (DOAS) method is presented. The technique is called orthogonal optical absorption spectroscopy (OOAS). A widespread variant of DOAS with smoothing of the registered spectrum and absorption cross sections being made employing a polynomial regression is a particular case of OOAS. The concept of OOAS provides a variety of new possibilities for constructing computational schemes and analyzing the influence of different error sources on calculated concentrations. PMID:25320931

  7. [The Establishment of the Method of the Fiber Optic Chemical Sensor Synchronous Absorption-Fluorescence].

    Zhang Li-hua; Iburaim, Arkin

    2016-03-01

    A new method of simultaneously measuring fiber-optic chemical sensor absorption spectrum and fluorescence spectrum is established. Make synchronous absorption-fluorescence cuvette, establish synchronous absorption-fluorescence spectrometry instrumentation combined by fiber optic chemical sensor technology, measure the synchronous absorption-fluorescence spectrums of solutions of rhodamine B, vitamin B2 and vitamin B6, compared by absorption spectroscopy measured by traditional UV-Visible photometric method and fluorescence spectroscopy measured by traditional fluorescence method. Synchronous absorption-fluorescence method measure absorption spectrums and fluorescence spectrums the same to traditional photometric and fluorescence spectroscopy of rhodamine B, vitamin B2 and vitamin B6. The maximum wavelength of fluorescence intensity method has high accuracy relatively compared with fluorescence, but the maximum wavelength of absorption has a slight deviation. Synchronous absorption-fluorescence method means simultaneously measure the absorption spectrums and fluorescence spectrums of the fluorescent substance, making two spectrums to one. The method measured the maximum emission wavelength with high accuracy, though in measuring maximum absorption wavelength there is a slight deviation, but it is worth further studying. PMID:27400519

  8. Theory of attosecond absorption spectroscopy in krypton

    Baggesen, Jan Conrad; Lindroth, Eva; Madsen, Lars Bojer

    2012-01-01

    A theory for time-domain attosecond pump–attosecond probe photoabsorption spectroscopy is formulated and related to the atomic response. The theory is illustrated through a study of attosecond absorption spectroscopy in krypton. The atomic parameters entering the formulation such as energies and...... Auger widths, as well as wave functions and dipole coupling matrix elements, are determined by accurate many-body structure calculations. We create a hole in a valence shell by an attosecond pump, couple an inner-shell electron to the hole by an attosecond probe, and then monitor the formation of the...

  9. Absorption spectroscopy with quantum cascade lasers

    Kosterev, A. A.; Curl, R. F.; Tittel, F. K.; Gmachl, C.; Capasso, F.; Sivco, D. L.; Baillargeon, J. N.; Hutchinson, A. L.; Cho, A. Y.

    2001-01-01

    Novel pulsed and cw quantum cascade distributed feedback (QC-DFB) lasers operating near lambda=8 micrometers were used for detection and quantification of trace gases in ambient air by means of sensitive absorption spectroscopy. N2O, 12CH4, 13CH4, and different isotopic species of H2O were detected. Also, a highly selective detection of ethanol vapor in air with a sensitivity of 125 parts per billion by volume (ppb) was demonstrated.

  10. Multi axis differential optical absorption spectroscopy (MAX-DOAS)

    Hönninger, G.; Von Friedeburg, C.; U. Platt

    2004-01-01

    Multi Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) in the atmosphere is a novel measurement technique that represents a significant advance on the well-established zenith scattered sunlight DOAS instruments which are mainly sensitive to stratospheric absorbers. MAX-DOAS utilizes scattered sunlight received from multiple viewing directions. The spatial distribution of various trace gases close to the instrument can be derived by combining several viewing directions. Ground...

  11. Multi axis differential optical absorption spectroscopy (MAX-DOAS)

    Hönninger, G.; Friedeburg, C.; U. Platt

    2004-01-01

    Multi Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) in the atmosphere is a novel measurement technique that represents a significant advance on the well-established zenith scattered sunlight DOAS instruments which are mainly sensitive to stratospheric absorbers. MAX-DOAS utilizes scattered sunlight received from multiple viewing directions. The spatial distribution of various trace gases close to the instrument can be derived by combining sev...

  12. Absorption effects in diffusing wave spectroscopy.

    Sarmiento-Gomez, Erick; Morales-Cruzado, Beatriz; Castillo, Rolando

    2014-07-20

    The effect of absorption in diffusing wave spectroscopy (DWS) was studied using an absorption-dependent diffusive equation for describing the light propagation within a turbid liquid where dielectric microspheres have been embedded. Here, we propose an expression for the time-averaged light intensity autocorrelation function that correctly describes the time fluctuations for the scattered light, in the regime where the diffusion approximation accurately describes the light propagation. This correction was suspected previously, but it was not formally derived from a light diffusive equation. As in the case of no absorption, we obtained that time fluctuations of the scattered light can be related to the mean square displacement of the embedded particles. However, if a correction for absorption is not taken into account, the colloidal dynamics can be misinterpreted. Experimental results show that this new formulation correctly describes the time fluctuations of scattered light. This new procedure extends the applicability of DWS, and it opens the possibility of doing microrheology with this optical method in systems where absorption cannot be avoided. PMID:25090203

  13. Gas in scattering media absorption spectroscopy - GASMAS

    Svanberg, Sune

    2008-09-01

    An overview of the new field of Gas in Scattering Media Absorption Spectroscopy (GASMAS) is presented. GASMAS combines narrow-band diode-laser spectroscopy with diffuse media optical propagation. While solids and liquids have broad absorption features, free gas in pores and cavities in the material is characterized by sharp spectral signatures, typically 10,000 times sharper than those of the host material. Many applications in materials science, food packaging, pharmaceutics and medicine have been demonstrated. So far molecular oxygen and water vapour have been studied around 760 and 935 nm, respectively. Liquid water, an important constituent in many natural materials, such as tissue, has a low absorption at such wavelengths, allowing propagation. Polystyrene foam, wood, fruits, food-stuffs, pharmaceutical tablets, and human sinus cavities have been studied. Transport of gas in porous media can readily be studied by first immersing the material in, e.g., pure nitrogen, and then observing the rate at which normal air, containing oxygen, reinvades the material. The conductance of the sinus connective passages can be measured in this way by flushing the nasal cavity with nitrogen. Also other dynamic processes such as drying of materials can be studied. The techniques have also been extended to remote-sensing applications (LIDAR-GASMAS).

  14. Cavity-Enhanced Ultrafast Transient Absorption Spectroscopy

    Reber, Melanie A R; Allison, Thomas K

    2015-01-01

    We present a new technique using a frequency comb laser and optical cavities for performing ultrafast transient absorption spectroscopy with improved sensitivity. Resonantly enhancing the probe pulses, we demonstrate a sensitivity of $\\Delta$OD $ = 1 \\times 10^{-9}/\\sqrt{\\mbox{Hz}}$ for averaging times as long as 30 s per delay point ($\\Delta$OD$_{min} = 2 \\times 10^{-10}$). Resonantly enhancing the pump pulses allows us to produce a high excitation fraction at high repetition-rate, so that signals can be recorded from samples with optical densities as low as OD $\\approx 10^{-8}$, or column densities $< 10^{10}$ molecules/cm$^2$. This high sensitivity enables new directions for ultrafast spectroscopy.

  15. X-ray absorption spectroscopy of semiconductors

    Ridgway, Mark

    2015-01-01

    X-ray Absorption Spectroscopy (XAS) is a powerful technique with which to probe the properties of matter, equally applicable to the solid, liquid and gas phases. Semiconductors are arguably our most technologically-relevant group of materials given they form the basis of the electronic and photonic devices that now so widely permeate almost every aspect of our society. The most effective utilisation of these materials today and tomorrow necessitates a detailed knowledge of their structural and vibrational properties. Through a series of comprehensive reviews, this book demonstrates the versatility of XAS for semiconductor materials analysis and presents important research activities in this ever growing field. A short introduction of the technique, aimed primarily at XAS newcomers, is followed by twenty independent chapters dedicated to distinct groups of materials. Topics span dopants in crystalline semiconductors and disorder in amorphous semiconductors to alloys and nanometric material as well as in-sit...

  16. Isotope analysis by infrared laser absorption spectroscopy

    The feasibility of IR laser spectroscopy as a technique for the measurement of small abundances of stable and radioactive isotopes has been examined. Theoretical considerations and first experimental results with two laser systems are presented: 1) Coincidences between emission lines of a CO2-laser and absorption lines of 13C-subsituted ethylene can be used to determine the 13C-concentration of C2H4. 2) A tunable PbS-diode laser emitting in the 4.3 μm-spectral region of the rotation-vibration bands of CO2 can be used to determine abundances of 12C, 13C, 16O, 17O and 18O in small samples of CO2. With optimized performance, sensitivities up to 10-9-10-10 seem possible, and for higher abundances an accuracy of 10-3. This should allow geophysical isotope studies to be performed and it is hoped that the technique will eventually be applicable to measuring the activity of long-lived radioisotopes. (orig.)

  17. (EXAFS) X-ray absorption spectroscopy

    The technique EXAFS (Extended X-Ray Absorption Fine Structure) is presented and its applications using the synchrotron radiation as an incidente beam in Science of Materials and Biophysics are shown. (L.C.)

  18. Absorption and fluorescence spectroscopy on a smartphone

    Hossain, Md. Arafat; Canning, John; Cook, Kevin; Ast, Sandra; Rutledge, Peter J.; Jamalipour, Abbas

    2015-07-01

    A self-powered smartphone-based field-portable "dual" spectrometer has been developed for both absorption and fluorescence measurements. The smartphone's existing flash LED has sufficient optical irradiance to undertake absorption measurements within a 3D-printed case containing a low cost nano-imprinted polymer diffraction grating. A UV (λex ~ 370 nm) and VIS (λex ~ 450 nm) LED are wired into the circuit of the flash LED to provide an excitation source for fluorescence measurements. Using a customized app on the smartphone, measurements of absorption and fluorescence spectra are demonstrated using pH-sensitive and Zn2+-responsive probes. Detection over a 300 nm span with 0.42 nm/pixel spectral resolution is demonstrated. Despite the low cost and small size of the portable spectrometer, the results compare well with bench top instruments.

  19. Photonic sensing of the atmosphere by absorption spectroscopy

    Chemically reactive atmospheric species play a crucial role in tropospheric processes which affect regional air quality and global climate change. Contrary to long-lived species such as greenhouse gases, interference-free accurate and precise concentration assessments of strongly reactive short-lived species represent a real challenge. In this paper, we report on the recent progress in spectroscopic instrumental developments for monitoring of OH, NO3, HONO and NO2 by using modern photonic sources (Quantum Cascade Laser, distributed feedback diode laser, light emitting diode) in conjunction with high-sensitivity spectroscopic measurement techniques such as multi-pass cell based long optical path length absorption spectroscopy, wavelength-modulation enhanced off-axis integrated cavity output spectroscopy, Faraday rotation spectroscopy, incoherent broadband cavity enhanced absorption spectroscopy. The main techniques available for routine atmospheric measurements of OH, NO3 and HONO are overviewed, in comparison with the emerging modern photonic spectroscopy techniques.

  20. Photothermal Absorption Spectroscopy of Individual Semiconductor Nanocrystals

    Berciaud, Stéphane; Cognet, Laurent; Lounis, Brahim

    2007-01-01

    Photothermal heterodyne detection is used to record the first room-temperature absorption spectra of single CdSe/ZnS semiconductor nanocrystals. These spectra are recorded in the high cw excitation regime, and the observed bands are assigned to transitions involving biexciton and trion states. Comparison with the single nanocrystals photoluminescence spectra leads to the measurement of spectral Stokes shifts free from ensemble averaging.

  1. [Study of retrieving formaldehyde with differential optical absorption spectroscopy].

    Li, Yu-Jin; Xie, Pin-Hua; Qin, Min; Qu, Xiao-Ying; Hu, Lin

    2009-01-01

    The present paper introduces the method of retrieving the concentration of HCHO with differential optical absorption spectroscopy (DOAS). The authors measured ambient HCHO in Beijing region with the help of differential optical absorption spectroscopy instrument made by ourself, and discussed numerous factors in retrieving the concentration of HCHO with differential optical absorption spectroscopy (DOAS), especially, the choice of HCHO wave band, how to avoid absorption of ambient SO2, NO2 and O3, and the influence of the Xenon lamp spectrum structure on the absorption of ambient HCHO. The authors achieved the HCHO concentration by simultaneously retrieving the concentrations of HCHO, SO2, NO2 and O3 with non-linear least square fitting method, avoiding the effect of choosing narrow wave of HCHO and the residual of SO2, NO2, O3 and the Xenon lamp spectrum structure in retrieving process to attain the concentration of HCHO, Finally the authors analyzed the origin of error in retrieving the concentration of HCHO with differential optical absorption spectroscopy (DOAS), and the total error is within 13.7% in this method. PMID:19385238

  2. Atomic absorption spectroscopy with high temperature flames.

    Willis, J B

    1968-07-01

    An account is given of the history of the development of high temperature flames for the atomic absorption measurement of metals forming refractory oxides. The principles governing the design of premix burners for such flames, and the relative merits of different types of nebulizer burner systems are described. After a brief account of the structure and emission characteristics of the premixed oxygen-acetylene and nitrous oxide-acetylene flames, the scope and limitations of the latter flame in chemical analysis are discussed. PMID:20068790

  3. Differential optical absorption spectroscopy principles and applications

    Platt, Ulrich; Imboden, Dieter

    2008-01-01

    Measurement techniques form the basis of our knowledge about atmospheric composition and chemistry. Presently, important questions of atmospheric chemistry center on urban pollution, free-radical chemistry, degradation of greenhouse gases and the budgets of tropospheric and stratospheric ozone. Among the many different optical spectroscopic methods that are in use, DOAS has emerged as a universal technique to measure the concentrations of atmospheric trace gases by making use of the characteristic absorption features of gas molecules along a path of known length in the open atmosphere. This bo

  4. Optical technique for broadband microwave absorption spectroscopy in aqueous media

    Precise measurements of microwave absorption over a large range of frequencies in aqueous media are difficult to obtain and can result in conflicting results as a consequences of small differences in instrumentation. Traditional methods of microwave spectroscopy that make use of time-domain spectrometers or network analyzer systems provide only indirect measurement of the microwave absorption coefficient because they measure the real and imaginary parts of the dielectric constant, ε' and ε'', separately. The absorption coefficient must then be calculated from ε' and ε'' taking into account the geometry (e.g., of the waveguide and mode) among other factors. It has been shown that direct measurement of the microwave absorption coefficient α is possible using phase fluctuation optical heterodyne spectroscopy. Taking advantage of this hybrid optical-microwave technique the authors report on a broadband spectrometer with demonstrated accurate operation from 3 to 20 GHz

  5. Speciesion arsenic and selenium using hydride method atomic absorption spectroscopy

    Hydrides production - atomic absorption spectroscopy system was studied. Hydrides production tool and gas-liquid separator were tested and successfully used in this work. Hydride was produced through natrium borohydride reaction with sample solution. Emitted gas was separated by gas-liquid separator before it is carried by nitrogen gas through T tube which is put in atomic absorption flame spectrophotometer. Efficiency of the system was tested through standard reference sample and seawater / sediment samples which is collected from Negeri Johor water bays

  6. Absorption spectroscopy of laser excited europium vapour

    Absorption spectra of europium vapour irradiated by intense, monochromatic resonance radiation at the wavelengths of the three principal resonance lines, 4f76s2, 8S(J=7/2)→4f76s6p, y 8P(J=5/2, 7/2 and 9/2) at 466.2, 462.7 and 459.4 nm respectively, have been photographed at high resolution. Pulsed resonance radiation was obtained from a tunable, narrow-band dye laser pumped by a nitrogen laser: a broad-band dye laser pumped by the same nitrogen laser provided background radiation. Our spectra covered the ranges 380-400 nm, and 410-450 nm, each one showing transitions from a single resonance level to upper levels in the region of either the 4f76s, 7S or the 4f76s, 9S ionization limit of EuII. In the shorter wavelength range the spectra consisted of weak autoionized series converging towards the 7S limit. In the longer wavelength range the three spectra were surprisingly dissimilar. The majority of the upper levels could be arranged into five highly-perturbed series, one corresponding to each of the J values 3/2, 5/2, 7/2, 9/2 and 11/2. These series arose from excitation of the 6p electron to high lying d-orbitals. The absorption transitions to the series members are only prominent in regions where the series are strongly perturbed, indicating that most of the line strength is derived from the perturbing levels. Possible origins for the perturbing levels are discussed. Little evidence was found for a series arising from excitation of the 6p electron to high lying s-orbitals. (author)

  7. Infrared laser spectroscopy using a long pathlength absorption cell

    The authors developed two very long pathlength absorption cells to be used in conjunction with diode lasers. They were designed to operate at controlled temperatures with the optical pathlength variable up to approx. 1,5 Km. Not only very low sample pressures are used for studies with such cells but also the spectroscopic sensitivity is enhanced over conventional methods by a factor of 103 to 104. In this paper they present some analytical aspects of the diode laser spectroscopy using the long pathlength absorption cells in the areas of absorption line widths, pressure broadening coefficients, isotope composition measurements and trace impurity analysis

  8. Procedure for intercomparison study for trace elements determination in soil samples by absorption spectroscopy

    In the environmental sampling analysis there is very important to establish an adequate methodologies on the laboratories for improvement the quality of the results obtained, so the establishment of a qualified laboratories network for environmental analysis. The objective of this work is to show the working plan for the analysis of eight elements on a Russian soil sample for an interlaboratory comparison with IAEA, by the Absorption spectroscopy technique using flame. (Author)

  9. Absorption and Emission Spectroscopy of a Lasing Material: Ruby

    Esposti, C. Degli; Bizzocchi, L.

    2007-01-01

    Ruby is a crystalline material, which comes very expensive and is of great significance, as it helped in the creation of first laser. An experiment to determine the absorption and emission spectroscopy, in addition to the determination of the room-temperature lifetime of the substance is being described.

  10. Developing a Transdisciplinary Teaching Implement for Atomic Absorption Spectroscopy

    Drew, John

    2008-01-01

    In this article I explain why I wrote the set of teaching notes on Atomic Absorption Spectroscopy (AAS) and why they look the way they do. The notes were intended as a student reference to question, highlight and write over as much as they wish during an initial practical demonstration of the threshold concept being introduced, in this case…

  11. Laser photothermal spectroscopy of light-induced absorption

    Skvortsov, L A [Institute of Cryptography, Communications and Informatics, Moscow (Russian Federation)

    2013-01-31

    Basic methods of laser photothermal spectroscopy, which are used to study photoinduced absorption in various media, are briefly considered. Comparative analysis of these methods is performed and the latest results obtained in this field are discussed. Different schemes and examples of their practical implementation are considered. (review)

  12. Multi axis differential optical absorption spectroscopy (MAX-DOAS

    G. Hönninger

    2004-01-01

    Full Text Available Multi Axis Differential Optical Absorption Spectroscopy (MAX-DOAS in the atmosphere is a novel measurement technique that represents a significant advance on the well-established zenith scattered sunlight DOAS instruments which are mainly sensitive to stratospheric absorbers. MAX-DOAS utilizes scattered sunlight received from multiple viewing directions. The spatial distribution of various trace gases close to the instrument can be derived by combining several viewing directions. Ground based MAX-DOAS is highly sensitive to absorbers in the lowest few kilometres of the atmosphere and vertical profile information can be retrieved by combining the measurements with Radiative Transfer Model (RTM calculations. The potential of the technique for a wide variety of studies of tropospheric trace species and its (few limitations are discussed. A Monte Carlo RTM is applied to calculate Airmass Factors (AMF for the various viewing geometries of MAX-DOAS. Airmass Factors can be used to quantify the light path length within the absorber layers. The airmass factor dependencies on the viewing direction and the influence of several parameters (trace gas profile, ground albedo, aerosol profile and type, solar zenith and azimuth angles are investigated. In addition we give a brief description of the instrumental MAX-DOAS systems realised and deployed so far. The results of the RTM studies are compared to several examples of recent MAX-DOAS field experiments and an outlook for future possible applications is given.

  13. Communication: XUV transient absorption spectroscopy of iodomethane and iodobenzene photodissociation

    Drescher, L.; Galbraith, M. C. E.; Reitsma, G.; Dura, J.; Zhavoronkov, N.; Patchkovskii, S.; Vrakking, M. J. J.; Mikosch, J.

    2016-07-01

    Time-resolved extreme ultraviolet (XUV) transient absorption spectroscopy of iodomethane and iodobenzene photodissociation at the iodine pre-N4,5 edge is presented, using femtosecond UV pump pulses and XUV probe pulses from high harmonic generation. For both molecules the molecular core-to-valence absorption lines fade immediately, within the pump-probe time-resolution. Absorption lines converging to the atomic iodine product emerge promptly in CH3I but are time-delayed in C6H5I. We attribute this delay to the initial π → σ* excitation in iodobenzene, which is distant from the iodine reporter atom. We measure a continuous shift in energy of the emerging atomic absorption lines in CH3I, attributed to relaxation of the excited valence shell. An independent particle model is used to rationalize the observed experimental findings.

  14. Estimation of molar absorptivities and pigment sizes for eumelanin and pheomelanin using femtosecond transient absorption spectroscopy

    Piletic, Ivan R.; Matthews, Thomas E.; Warren, Warren S.

    2009-11-01

    Fundamental optical and structural properties of melanins are not well understood due to their poor solubility characteristics and the chemical disorder present during biomolecular synthesis. We apply nonlinear transient absorption spectroscopy to quantify molar absorptivities for eumelanin and pheomelanin and thereby get an estimate for their average pigment sizes. We determine that pheomelanin exhibits a larger molar absorptivity at near IR wavelengths (750nm), which may be extended to shorter wavelengths. Using the molar absorptivities, we estimate that melanin pigments contain ˜46 and 28 monomer units for eumelanin and pheomelanin, respectively. This is considerably larger than the oligomeric species that have been recently proposed to account for the absorption spectrum of eumelanin and illustrates that larger pigments comprise a significant fraction of the pigment distribution.

  15. Using a high finesse optical resonator to provide a long light path for differential optical absorption spectroscopy: CE-DOAS

    J. Meinen; J. Thieser; U. Platt; T. Leisner

    2008-01-01

    Cavity enhanced methods in absorption spectroscopy have seen a considerable increase in popularity during the past decade. Especially Cavity Enhanced Absorption Spectroscopy (CEAS) established itself in atmospheric trace gas detection by providing tens of kilometers of effective light path length using a cavity as short as 1 m. In this paper we report on the construction and testing of a compact and power efficient light emitting diode based broadband Cavity Enhanced Differential Optical Abso...

  16. Light-induced changes in subband absorption in a-Si:H using photoluminescence absorption spectroscopy

    Gu, S. Q.; Taylor, P. C.; Nitta, S.

    1991-08-01

    We have used the photoluminescence (PL) generated in a thin-film sample of a-Si:H to probe low absorption levels by measuring the absorption of the PL as it travels down the length of the film in a waveguide mode. This technique, which we have called PL absorption spectroscopy of PLAS, allows the measurement of values of the absorption coefficient α down to about 0.1 cm-1. Because this technique probes the top and bottom surfaces of the a-Si:H sample, it is important to separate surface from bulk absorption mechanisms. An improved sample geometry has been employed to facilitate this separation. One sample consisted of an a-Si1-xNix:H/a-Si:H/ a-Si1-xNx:H/NiCr layered structure where the silicon nitride layers served as the cladding layers for the waveguide. In a second sample the a-Si:H layer was interrupted near the middle for two separate, thin (100 Å) layers of a-Si1-xNx:H in order to check for the importance of the absorption at the silicon/silicon nitride interfaces in these PLAS measurements. Changes in the below-gap absorption on light soaking were examined using irradiation from an Ar+ laser (5145 Å, ˜200 mW/cm2 for 5.5 hours at 300 K). The silicon/silicon nitride interface is responsible for an absorption which has a shoulder near 1.2 eV while the bulk a-Si:H absorption exhibits no such shoulder. The metastable, optically-induced increase in the below gap absorption appears to come entirely from the bulk of the a-Si:H. These low temperature PLAS measurements are compared with those obtained at 300 K by photothermal deflection spectroscopy.

  17. Transient x-ray absorption spectroscopy of hydrated halogen atom

    Elles, Christopher G; Crowell, Robert A; Arms, Dohn A; Landahl, Eric C

    2007-01-01

    Time-resolved x-ray absorption spectroscopy monitors the transient species generated by one-photon detachment of an electron from aqueous bromide. Hydrated bromine atoms with a lifetime of ca. 17 ns were observed, nearly half of which react with excess Br- to form Br2-. The K-edge spectra of the Br atom and Br2- anion exhibit distinctive resonant transitions that are absent for the Br- precursor. The absorption spectra indicate that the solvent shell around a Br0 atom is defined primarily by hydrophobic interactions, in agreement with a Monte Carlo simulation of the solvent structure.

  18. Infrared absorption spectroscopy and chemical kinetics of free radicals

    Curl, R.F.; Glass, G.P. [Rice Univ., Houston, TX (United States)

    1993-12-01

    This research is directed at the detection, monitoring, and study of chemical kinetic behavior by infrared absorption spectroscopy of small free radical species thought to be important intermediates in combustion. During the last year, infrared kinetic spectroscopy using excimer laser flash photolysis and color-center laser probing has been employed to study the high resolution spectrum of HCCN, the rate constant of the reaction between ethynyl (C{sub 2}H) radical and H{sub 2} in the temperature region between 295 and 875 K, and the recombination rate of propargyl (CH{sub 2}CCH) at room temperature.

  19. CO2 Spectroscopy Evaluation Using Atmospheric Solar Absorption Spectra

    Sen, Bhaswar; Brown, Linda R.; Miller, Charles E.; Toon, Geoffrey C.; Toth, Robert A.; Washenfelder, Rebecca A.; Wennberg, Paul O

    2006-01-01

    We evaluated the improvements in successive versions (1996 - 2004) of HITRAN (1) and other molecular line parameter data set (2) to correctly simulate infrared (IR) and near-infrared (NIR) CO 2 transmittance spectra. Understanding the global sources and sinks of CO 2 requires highly accurate measurements (ó 0.3%) and makes extreme de- mands on the spectroscopy. We evaluated the line parameter data sets by fitting solar absorption spectra measured by the JPL MkIV FTIR spectrometer (3) and the ...

  20. APPLICATION OF ABSORPTION SPECTROSCOPY TO ACTINIDE PROCESS ANALYSIS AND MONITORING

    Lascola, R.; Sharma, V.

    2010-06-03

    The characteristic strong colors of aqueous actinide solutions form the basis of analytical techniques for actinides based on absorption spectroscopy. Colorimetric measurements of samples from processing activities have been used for at least half a century. This seemingly mature technology has been recently revitalized by developments in chemometric data analysis. Where reliable measurements could formerly only be obtained under well-defined conditions, modern methods are robust with respect to variations in acidity, concentration of complexants and spectral interferents, and temperature. This paper describes two examples of the use of process absorption spectroscopy for Pu analysis at the Savannah River Site, in Aiken, SC. In one example, custom optical filters allow accurate colorimetric measurements of Pu in a stream with rapid nitric acid variation. The second example demonstrates simultaneous measurement of Pu and U by chemometric treatment of absorption spectra. The paper concludes with a description of the use of these analyzers to supplement existing technologies in nuclear materials monitoring in processing, reprocessing, and storage facilities.

  1. Pathlength Determination for Gas in Scattering Media Absorption Spectroscopy

    Liang Mei

    2014-02-01

    Full Text Available Gas in scattering media absorption spectroscopy (GASMAS has been extensively studied and applied during recent years in, e.g., food packaging, human sinus monitoring, gas diffusion studies, and pharmaceutical tablet characterization. The focus has been on the evaluation of the gas absorption pathlength in porous media, which a priori is unknown due to heavy light scattering. In this paper, three different approaches are summarized. One possibility is to simultaneously monitor another gas with known concentration (e.g., water vapor, the pathlength of which can then be obtained and used for the target gas (e.g., oxygen to retrieve its concentration. The second approach is to measure the mean optical pathlength or physical pathlength with other methods, including time-of-flight spectroscopy, frequency-modulated light scattering interferometry and the frequency domain photon migration method. By utilizing these methods, an average concentration can be obtained and the porosities of the material are studied. The last method retrieves the gas concentration without knowing its pathlength by analyzing the gas absorption line shape, which depends upon the concentration of buffer gases due to intermolecular collisions. The pathlength enhancement effect due to multiple scattering enables also the use of porous media as multipass gas cells for trace gas monitoring. All these efforts open up a multitude of different applications for the GASMAS technique.

  2. Study on the elemental mercury absorption cross section based on differential optical absorption spectroscopy

    Zheng, Haiming; Yao, Penghui

    2015-08-01

    With the method of ultraviolet absorption spectrum, the exact absorption cross-section with the light source of the low-pressure mercury lamp was determined, during which the optimum wavelength for mercury concentrations inversion was 253.69 nm, the highest detection limit was 0.177 μg/cm3, and the lowest detection limit was 0.034 μg/cm3. Furthermore, based on the differential optical absorption spectroscopy(DOAS), the relationship between the integral parameters (IP) and the concentration as well as the signal-noise ration (SNR) under the conditions of gas flow was determined and the lowest detection limit was figured out to be 0.03524 μg/cm3, providing a method of DOAS to de-noise through the comparison between the mercury concentration values produced by DOAS and that produced by the wavelet de-noising method (db5). It turned out that the differential optical absorption spectroscopy had a strong anti-interference ability, while the wavelet de-noising method was not suitable for measuring the trace concentration change.

  3. Diagnostic potential of cosmic-neutrino absorption spectroscopy

    Barenboim, Gabriela; /Valencia U.; Mena Requejo, Olga; Quigg, Chris; /Fermilab

    2004-12-01

    Annihilation of extremely energetic cosmic neutrinos on the relic-neutrino background can give rise to absorption lines at energies corresponding to formation of the electroweak gauge boson Z{sup 0}. The positions of the absorption dips are set by the masses of the relic neutrinos. Suitably intense sources of extremely energetic (10{sup 21} - 10{sup 25}-eV) cosmic neutrinos might therefore enable the determination of the absolute neutrino masses and the flavor composition of the mass eigenstates. Several factors--other than neutrino mass and composition--distort the absorption lines, however. We analyze the influence of the time-evolution of the relic-neutrino density and the consequences of neutrino decay. We consider the sensitivity of the lineshape to the age and character of extremely energetic neutrino sources, and to the thermal history of the Universe, reflected in the expansion rate. We take into account Fermi motion arising from the thermal distribution of the relic-neutrino gas. We also note the implications of Dirac vs. Majorana relics, and briefly consider unconventional neutrino histories. We ask what kinds of external information would enhance the potential of cosmic-neutrino absorption spectroscopy, and estimate the sensitivity required to make the technique a reality.

  4. Diagnostic potential of cosmic-neutrino absorption spectroscopy

    Annihilation of extremely energetic cosmic neutrinos on the relic-neutrino background can give rise to absorption lines at energies corresponding to formation of the electroweak gauge boson Z0. The positions of the absorption dips are set by the masses of the relic neutrinos. Suitably intense sources of extremely energetic (1021-1025-eV) cosmic neutrinos might therefore enable the determination of the absolute neutrino masses and the flavor composition of the mass eigenstates. Several factors--other than neutrino mass and composition--distort the absorption lines, however. We analyze the influence of the time evolution of the relic-neutrino density and the consequences of neutrino decay. We consider the sensitivity of the line shape to the age and character of extremely energetic neutrino sources, and to the thermal history of the Universe, reflected in the expansion rate. We take into account Fermi motion arising from the thermal distribution of the relic-neutrino gas. We also note the implications of Dirac vs. Majorana relics, and briefly consider unconventional neutrino histories. We ask what kinds of external information would enhance the potential of cosmic-neutrino absorption spectroscopy, and estimate the sensitivity required to make the technique a reality

  5. Operando X-ray absorption and infrared fuel cell spectroscopy

    Lewis, Emily A.; Kendrick, Ian; Jia, Qingying; Grice, Corey; Segre, Carlo U.; Smotkin, Eugene S. (NuVant); (IIT); (NEU)

    2011-11-17

    A polymer electrolyte fuel cell enables operando X-ray absorption and infrared spectroscopy of the membrane electrode assembly catalytic layer with flowing fuel and air streams at controlled temperature. Time-dependent X-ray absorption near edge structure spectra of the Pt and Ni edge of Pt based catalysts of an air-breathing cathode show that catalyst restructuring, after a potential step, has time constants from minutes to hours. The infrared Stark tuning plots of CO adsorbed on Pt at 100, 200, 300 and 400 mV vs. hydrogen reference electrode were obtained. The Stark tuning plots of CO adsorbed at 400 mV exhibit a precipitous drop in frequency coincident with the adsorption potential. The turn-down potential decreases relative to the adsorption potential and is approximately constant after 300 mV. These Stark tuning characteristics are attributed to potential dependent adsorption site selection by CO and competitive adsorption processes.

  6. [The Diagnostics of Detonation Flow External Field Based on Multispectral Absorption Spectroscopy Technology].

    Lü, Xiao-jing; Li, Ning; Weng, Chun-sheng

    2016-03-01

    Compared with traditional sampling-based sensing method, absorption spectroscopy technology is well suitable for detonation flow diagnostics, since it can provide with us fast response, nonintrusive, sensitive solution for situ measurements of multiple flow-field parameters. The temperature and concentration test results are the average values along the laser path with traditional absorption spectroscopy technology, while the boundary of detonation flow external field is unknown and it changes all the time during the detonation engine works, traditional absorption spectroscopy technology is no longer suitable for detonation diagnostics. The trend of line strength with temperature varies with different absorption lines. By increasing the number of absorption lines in the test path, more information of the non-uniform flow field can be obtained. In this paper, based on multispectral absorption technology, the reconstructed model of detonation flow external field distribution was established according to the simulation results of space-time conservation element and solution element method, and a diagnostic method of detonation flow external field was given. The model deviation and calculation error of the least squares method adopted were studied by simulation, and the maximum concentration and temperature calculation error was 20.1% and 3.2%, respectively. Four absorption lines of H2O were chosen and detonation flow was scanned at the same time. The detonation external flow testing system was set up for the valveless gas-liquid continuous pulse detonation engine with the diameter of 80 mm. Through scanning H2O absorption lines with a high frequency of 10 kHz, the on-line detection of detonation external flow was realized by direct absorption method combined with time-division multiplexing technology, and the reconstruction of dynamic temperature distribution was realized as well for the first time, both verifying the feasibility of the test method. The test results

  7. Fingerprints of polycyclic aromatic hydrocarbons (PAHs) in infrared absorption spectroscopy

    Tommasini, Matteo; Lucotti, Andrea; Alfè, Michela; Ciajolo, Anna; Zerbi, Giuseppe

    2016-01-01

    We have analyzed a set of 51 PAHs whose structures have been hypothesized from mass spectrometry data collected on samples extracted from carbon particles of combustion origin. We have obtained relationships between infrared absorption signals in the fingerprint region (mid-IR) and the chemical structures of PAHs, thus proving the potential of IR spectroscopy for the characterization of the molecular structure of aromatic combustion products. The results obtained here for the spectroscopic characterization of PAHs can be also of interest in Materials Science and Astrophysics.

  8. High Resolution Spectroscopy on an X-ray Absorption Beamline

    Hazemann, Jean-Louis; Proux, Olivier; Nassif, Vivian; Palancher, Hervé; Lahera, Eric; Da Silva, Cécile; Braillard, Aurélien; Testemale, Denis; Diot, Marie-Ange; Alliot, Isabelle; Delnet, William; Manceau, A.; Gélébart, Frédéric; Morand, Marc; Dermigny, Quentin

    2008-01-01

    Abstract A bent crystal spectrometer based on the Rowland circle geometry has been tested on the BM30b/FAME beamline at the European Synchrotron Radiation Facility. The energy resolution of the spectrometer (1.3eV at the Cu K1 energy, i.e. 8047.78eV) allows to perform different kinds of measurements, including X-ray Absorption Spectroscopy, Resonant Inelastic X-ray Scattering and X-ray Raman Scattering experiments. The simplicity of the experimental device makes it easily implemented on a cl...

  9. Study on Differential Optical Absorption Spectroscopy : Technique and its Applications

    Liu, Jianguo

    2002-01-01

    ln the first part of speech, with a description of the principle of DOAS (Differential Optical Absorption Spectroscopy), the design and realization of two different kinds of DOAS systems are nresented. 0ne is using a slotted disc raoid scanning device with a photomultiplier, which is suitable for ambient air quality measurement. It can measure total 16 kinds of pollutants such as SO_2, NO, N02, NH_3, O_3, C_6H_6, C_7H_8 and CH_2O etc., with detection limits of 1-2ppb. The other is using a UV ...

  10. Mid-infrared absorption spectroscopy using quantum cascade lasers

    Haibach, Fred; Erlich, Adam; Deutsch, Erik

    2011-06-01

    Block Engineering has developed an absorption spectroscopy system based on widely tunable Quantum Cascade Lasers (QCL). The QCL spectrometer rapidly cycles through a user-selected range in the mid-infrared spectrum, between 6 to 12 μm (1667 to 833 cm-1), to detect and identify substances on surfaces based on their absorption characteristics from a standoff distance of up to 2 feet with an eye-safe laser. It can also analyze vapors and liquids in a single device. For military applications, the QCL spectrometer has demonstrated trace explosive, chemical warfare agent (CWA), and toxic industrial chemical (TIC) detection and analysis. The QCL's higher power density enables measurements from diffuse and highly absorbing materials and substrates. Other advantages over Fourier Transform Infrared (FTIR) spectroscopy include portability, ruggedness, rapid analysis, and the ability to function from a distance through free space or a fiber optic probe. This paper will discuss the basic technology behind the system and the empirical data on various safety and security applications.

  11. [Retrieval of monocyclic aromatic hydrocarbons with differential optical absorption spectroscopy].

    Xie, Pin-Hua; Fu, Qiang; Liu, Jian-Guo; Liu, Wen-Qing; Qin, Min; Li, Ang; Liu, Shi-Sheng; Wei, Qing-Nong

    2006-09-01

    Differential optical absorption spectroscopy (DOAS) technique has been used to measure trace gases in the atmosphere by their strongly structured absorption of radiation in the UV and visible spectral range, e. g. SO2, NO2, O3 etc. However, unlike the absorption spectra of SO2 and NO2, the analysis of aromatic compounds is difficult and strongly suffers from the cross interference of other absorbers (Herzberg bands of oxygen, ozone and sulfur dioxide), especially with relatively low concentrations of aromatic compounds in the atmosphere. In the present paper, the DOAS evaluation of aromatic compounds was performed by nonlinear least square fit with two interpolated oxygen optical density spectra at different path lengths and reference spectra of ozone at different temperature and SO2 cross section to correct the interference from absorbers of O2, O3 and SO2. The measurement of toluene, benzene, (m, p, o) xylene and phenol with a DOAS system showed that DOAS method is suitable for monocyclic aromatic compounds monitoring in the atmosphere. PMID:17112022

  12. Femtosecond transient absorption spectroscopy of silanized silicon quantum dots

    Kuntermann, Volker; Cimpean, Carla; Brehm, Georg; Sauer, Guido; Kryschi, Carola; Wiggers, Hartmut

    2008-03-01

    Excitonic properties of colloidal silicon quantum dots (Si qdots) with mean sizes of 4nm were examined using stationary and time-resolved optical spectroscopy. Chemically stable silicon oxide shells were prepared by controlled surface oxidation and silanization of HF-etched Si qdots. The ultrafast relaxation dynamics of photogenerated excitons in Si qdot colloids were studied on the picosecond time scale from 0.3psto2.3ns using femtosecond-resolved transient absorption spectroscopy. The time evolution of the transient absorption spectra of the Si qdots excited with a 150fs pump pulse at 390nm was observed to consist of decays of various absorption transitions of photoexcited electrons in the conduction band which overlap with both the photoluminescence and the photobleaching of the valence band population density. Gaussian deconvolution of the spectroscopic data allowed for disentangling various carrier relaxation processes involving electron-phonon and phonon-phonon scatterings or arising from surface-state trapping. The initial energy and momentum relaxation of hot carriers was observed to take place via scattering by optical phonons within 0.6ps . Exciton capturing by surface states forming shallow traps in the amorphous SiOx shell was found to occur with a time constant of 4ps , whereas deeper traps presumably localized in the Si-SiOx interface gave rise to exciton trapping processes with time constants of 110 and 180ps . Electron transfer from initially populated, higher-lying surface states to the conduction band of Si qdots (>2nm) was observed to take place within 400 or 700fs .

  13. Optical re-injection in cavity-enhanced absorption spectroscopy

    Leen, J. Brian, E-mail: b.leen@lgrinc.com; O’Keefe, Anthony [Los Gatos Research, 67 E. Evelyn Avenue, Suite 3, Mountain View, California 94041 (United States)

    2014-09-15

    Non-mode-matched cavity-enhanced absorption spectrometry (e.g., cavity ringdown spectroscopy and integrated cavity output spectroscopy) is commonly used for the ultrasensitive detection of trace gases. These techniques are attractive for their simplicity and robustness, but their performance may be limited by the reflection of light from the front mirror and the resulting low optical transmission. Although this low transmitted power can sometimes be overcome with higher power lasers and lower noise detectors (e.g., in the near-infrared), many regimes exist where the available light intensity or photodetector sensitivity limits instrument performance (e.g., in the mid-infrared). In this article, we describe a method of repeatedly re-injecting light reflected off the front mirror of the optical cavity to boost the cavity's circulating power and deliver more light to the photodetector and thus increase the signal-to-noise ratio of the absorption measurement. We model and experimentally demonstrate the method's performance using off-axis cavity ringdown spectroscopy (OA-CRDS) with a broadly tunable external cavity quantum cascade laser. The power coupled through the cavity to the detector is increased by a factor of 22.5. The cavity loss is measured with a precision of 2 × 10{sup −10} cm{sup −1}/√(Hz;) an increase of 12 times over the standard off-axis configuration without reinjection and comparable to the best reported sensitivities in the mid-infrared. Finally, the re-injected CRDS system is used to measure the spectrum of several volatile organic compounds, demonstrating the improved ability to resolve weakly absorbing spectroscopic features.

  14. Optical re-injection in cavity-enhanced absorption spectroscopy

    Leen, J. Brian; O’Keefe, Anthony

    2014-01-01

    Non-mode-matched cavity-enhanced absorption spectrometry (e.g., cavity ringdown spectroscopy and integrated cavity output spectroscopy) is commonly used for the ultrasensitive detection of trace gases. These techniques are attractive for their simplicity and robustness, but their performance may be limited by the reflection of light from the front mirror and the resulting low optical transmission. Although this low transmitted power can sometimes be overcome with higher power lasers and lower noise detectors (e.g., in the near-infrared), many regimes exist where the available light intensity or photodetector sensitivity limits instrument performance (e.g., in the mid-infrared). In this article, we describe a method of repeatedly re-injecting light reflected off the front mirror of the optical cavity to boost the cavity's circulating power and deliver more light to the photodetector and thus increase the signal-to-noise ratio of the absorption measurement. We model and experimentally demonstrate the method's performance using off-axis cavity ringdown spectroscopy (OA-CRDS) with a broadly tunable external cavity quantum cascade laser. The power coupled through the cavity to the detector is increased by a factor of 22.5. The cavity loss is measured with a precision of 2 × 10−10 cm−1/\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{upgreek} \\usepackage{mathrsfs} \\setlength{\\oddsidemargin}{-69pt} \\begin{document} }{}$\\sqrt {{\\rm Hz;}}$\\end{document} Hz ; an increase of 12 times over the standard off-axis configuration without reinjection and comparable to the best reported sensitivities in the mid-infrared. Finally, the re-injected CRDS system is used to measure the spectrum of several volatile organic compounds, demonstrating the improved ability to resolve weakly absorbing spectroscopic features. PMID:25273701

  15. Investigating Actinide Molecular Adducts From Absorption Edge Spectroscopy

    Den Auwer, C.; Conradson, S.D.; Guilbaud, P.; Moisy, P.; Mustre de Leon, J.; Simoni, E.; /SLAC, SSRL

    2006-10-27

    Although Absorption Edge Spectroscopy has been widely applied to the speciation of actinide elements, specifically at the L{sub III} edge, understanding and interpretation of actinide edge spectra are not complete. In that sense, semi-quantitative analysis is scarce. In this paper, different aspects of edge simulation are presented, including semi-quantitative approaches. Comparison is made between various actinyl (U, Np) aquo or hydroxy compounds. An excursion into transition metal osmium chemistry allows us to compare the structurally related osmyl and uranyl hydroxides. The edge shape and characteristic features are discussed within the multiple scattering picture and the role of the first coordination sphere as well as contributions from the water solvent are described.

  16. Arsenic speciation in solids using X-ray absorption spectroscopy

    Foster, Andrea L.; Kim, Chris S.

    2014-01-01

    Synchrotron-based X-ray absorption spectroscopy (XAS) is an in situ, minimally-destructive, element-specific, molecular-scale structural probe that has been employed to study the chemical forms (species) of arsenic (As) in solid and aqueous phases (including rocks, soils, sediment, synthetic compounds, and numerous types of biota including humans) for more than 20 years. Although several excellent reviews of As geochemistry and As speciation in the environment have been published previously (including recent contributions in this volume), the explosion of As-XAS studies over the past decade (especially studies employing microfocused X-ray beams) warrants this new review of the literature and of data analysis methods.

  17. Mercury pollution surveys in Riga by Zeeman atomic absorption spectroscopy

    Practical sessions of mercury pollution measurements in Riga (Latvia) have been performed in several districts using an RA-915+ Zeeman atomic absorption spectrometer coupled with a global positioning system (GPS). The measurements were taken from a driving car and in different days at one particular location (the Institute of Atomic Physics and Spectroscopy) for monitoring the changes in atmospheric mercury concentration. GPS was used to relate the measurement results to particular places, which made it possible to create a digitalized database of pollution for different geographic coordinates in different time spans. The measurements have shown that the background level of mercury concentration in Riga does not exceed 5 ng/m3, although there are several areas of elevated mercury pollution that need particular attention. (Authors)

  18. Simultaneous surface plasmon resonance and x-ray absorption spectroscopy

    Serrano, A. [Instituto de Ceramica y Vidrio (ICV-CSIC), Cantoblanco, 28049 Madrid (Spain); Departamento de Fisica de Materiales, Universidad Complutense de Madrid, 28040 Madrid (Spain); Rodriguez de la Fuente, O. [Departamento de Fisica de Materiales, Universidad Complutense de Madrid, 28040 Madrid (Spain); Collado, V.; Rubio-Zuazo, J.; Castro, G. R. [SpLine, Spanish CRG Beamline at the ESRF, F-38043 Grenoble, Cedex 09, France and Instituto de Ciencia de Materiales de Madrid, (ICMM-CSIC), Cantoblanco, 28049 Madrid (Spain); Monton, C. [Department of Physics and Center for Advanced Nanoscience, University of California San Diego, La Jolla, California 92093 (United States); Garcia, M. A. [Instituto de Ceramica y Vidrio (ICV-CSIC), Cantoblanco, 28049 Madrid (Spain); IMDEA Nanociencia, Cantoblanco, 28049 Madrid (Spain)

    2012-08-15

    We present an experimental setup for the simultaneous measurement of surface plasmon resonance (SPR) and x-ray absorption spectroscopy (XAS) on metallic thin films at a synchrotron beamline. The system allows measuring in situ and in real time the effect of x-ray irradiation on the SPR curves to explore the interaction of x-rays with matter. It is also possible to record XAS spectra while exciting SPR in order to study changes in the films induced by the excitation of surface plasmons. Combined experiments recording simultaneously SPR and XAS curves while scanning different parameters can be also carried out. The relative variations in the SPR and XAS spectra that can be detected with this setup range from 10{sup -3} to 10{sup -5}, depending on the particular experiment.

  19. Integrating cavity ring-down spectroscopy (ICRDS) and the direct measurement of absorption coefficients

    Fry, Edward S.; Mason, John D.

    2016-04-01

    Absorption of light at various wavelengths (i.e. absorption spectroscopy) is a powerful tool for identifying the presence of chemical compounds or specific substances in a sample. Cavity ring down spectroscopy (CRDS) is a well-known technique for very high sensitivity absorption spectroscopy. Another technique, integrating cavity spectroscopy has the additional unique feature of providing accurate absorption data even in the presence of severe scattering. This paper describes a combination of these two techniques that has led to an extremely powerful and useful new technology—integrating CRDS.

  20. High Dispersion Absorption-line Spectroscopy of AE Aqr

    Echevarria, J; Costero, R; Zharikov, S; Michel, R

    2008-01-01

    High-dispersion time-resolved spectroscopy of the unique magnetic cataclysmic variable AE Aqr is presented. A radial velocity analysis of the absorption lines yields K_2 = 168.7+/- 1 km/s. Substantial deviations of the radial velocity curve from a sinusoid are interpreted in terms of intensity variations over the secondary star's surface. A complex rotational velocity curve as a function of orbital phase is detected which has a modulation frequency of twice the orbital frequency, leading to an estimate of the binary inclination angle that is close to 70^o. The minimum and maximum rotational velocities are used to indirectly derive a mass ratio of q= 0.6 and a radial velocity semi-amplitude of the white dwarf of K_1 = 101+/-3 km/s. We present an atmospheric temperature indicator, based on the absorption line ratio of Fe I and Cr I lines, whose variation indicates that the secondary star varies from K0 to K4 as a function of orbital phase. The ephemeris of the system has been revised, using more than one thousa...

  1. Sulfur K-edge absorption spectroscopy on selected biological systems

    Sulfur is an essential element in organisms. In this thesis investigations of sulfur compounds in selected biological systems by XANES (X-ray Absorption Near Edge Structure) spectroscopy are reported. XANES spectroscopy at the sulfur K-edge provides an excellent tool to gain information about the local environments of sulfur atoms in intact biological samples - no extraction processes are required. Spatially resolved measurements using a Kirkpatrick-Baez mirror focusing system were carried out to investigate the infection of wheat leaves by rust fungi. The results give information about changes in the sulfur metabolism of the host induced by the parasite and about the extension of the infection into visibly uninfected plant tissue. Furthermore, XANES spectra of microbial mats from sulfidic caves were measured. These mats are dominated by microbial groups involved in cycling sulfur. Additionally, the influence of sulfate deprivation and H2S exposure on sulfur compounds in onion was investigated. To gain an insight into the thermal degradation of organic material the influence of roasting of sulfur compounds in coffee beans was studied. (orig.)

  2. Quantitative investigation of two metallohydrolases by X-ray absorption spectroscopy near-edge spectroscopy

    The last several years have witnessed a tremendous increase in biological applications using X-ray absorption spectroscopy (BioXAS), thanks to continuous advancements in synchrotron radiation (SR) sources and detector technology. However, XAS applications in many biological systems have been limited by the intrinsic limitations of the Extended X-ray Absorption Fine Structure (EXAFS) technique e.g., the lack of sensitivity to bond angles. As a consequence, the application of the X-ray absorption near-edge structure (XANES) spectroscopy changed this scenario that is now continuously changing with the introduction of the first quantitative XANES packages such as Minut XANES (MXAN). Here we present and discuss the XANES code MXAN, a novel XANES-fitting package that allows a quantitative analysis of experimental data applied to Zn K-edge spectra of two metalloproteins: Leptospira interrogans Peptide deformylase (LiPDF) and acutolysin-C, a representative of snake venom metalloproteinases (SVMPs) from Agkistrodon acutus venom. The analysis on these two metallohydrolases reveals that proteolytic activities are correlated to subtle conformation changes around the zinc ion. In particular, this quantitative study clarifies the occurrence of the LiPDF catalytic mechanism via a two-water-molecules model, whereas in the acutolysin-C we have observed a different proteolytic activity correlated to structural changes around the zinc ion induced by pH variations

  3. Quantitative investigation of two metallohydrolases by X-ray absorption spectroscopy near-edge spectroscopy

    Zhao, W. [Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027 (China); Chu, W.S.; Yang, F.F.; Yu, M.J.; Chen, D.L.; Guo, X.Y. [Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Zhou, D.W.; Shi, N. [Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027 (China); Marcelli, A. [Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati, P.O. Box 13, Frascati 00044 (Italy); Niu, L.W.; Teng, M.K. [Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui 230027 (China); Gong, W.M. [Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101 (China); Benfatto, M. [Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati, P.O. Box 13, Frascati 00044 (Italy); Wu, Z.Y. [Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati, P.O. Box 13, Frascati 00044 (Italy)], E-mail: wuzy@ihep.ac.cn

    2007-09-21

    The last several years have witnessed a tremendous increase in biological applications using X-ray absorption spectroscopy (BioXAS), thanks to continuous advancements in synchrotron radiation (SR) sources and detector technology. However, XAS applications in many biological systems have been limited by the intrinsic limitations of the Extended X-ray Absorption Fine Structure (EXAFS) technique e.g., the lack of sensitivity to bond angles. As a consequence, the application of the X-ray absorption near-edge structure (XANES) spectroscopy changed this scenario that is now continuously changing with the introduction of the first quantitative XANES packages such as Minut XANES (MXAN). Here we present and discuss the XANES code MXAN, a novel XANES-fitting package that allows a quantitative analysis of experimental data applied to Zn K-edge spectra of two metalloproteins: Leptospira interrogans Peptide deformylase (LiPDF) and acutolysin-C, a representative of snake venom metalloproteinases (SVMPs) from Agkistrodon acutus venom. The analysis on these two metallohydrolases reveals that proteolytic activities are correlated to subtle conformation changes around the zinc ion. In particular, this quantitative study clarifies the occurrence of the LiPDF catalytic mechanism via a two-water-molecules model, whereas in the acutolysin-C we have observed a different proteolytic activity correlated to structural changes around the zinc ion induced by pH variations.

  4. Gas in Scattering Media Absorption Spectroscopy -- Laser Spectroscopy in Unconventional Environments

    Svanberg, Sune

    2010-02-01

    An overview of the new field of Gas in Scattering Media Absorption Spectroscopy (GASMAS) is presented. The GASMAS technique combines narrow-band diode-laser spectroscopy with optical propagation in diffuse media. Whereas solids and liquids have broad absorption features, free gas in pores and cavities in the material is characterized by sharp spectral signatures. These are typically 10,000 times sharper than those of the host material. Many applications in materials science, food packaging, pharmaceutics and medicine have been demonstrated. Molecular oxygen and water vapor have been studied around 760 and 935 nm, respectively. Liquid water, an important constituent in many natural materials, such as tissue, has a low absorption at such wavelengths, allowing propagation. Polystyrene foam, wood, fruits, food-stuffs, pharmaceutical tablets, and human sinus cavities have been studied, demonstrating new possibilities for characterization and diagnostics. Transport of gas in porous media can readily be studied by first immersing the material in, e.g., pure nitrogen gas, and then observing the rate at which normal air, containing oxygen, reinvades the material. The conductance of the human sinus connective passages can be measured in this way by flushing the nasal cavity with nitrogen, while breathing normally through the mouth. A clinical study comprising 40 patients has been concluded.

  5. Cavity-Enhanced Absorption Spectroscopy and Photoacoustic Spectroscopy for Human Breath Analysis

    Wojtas, J.; Tittel, F. K.; Stacewicz, T.; Bielecki, Z.; Lewicki, R.; Mikolajczyk, J.; Nowakowski, M.; Szabra, D.; Stefanski, P.; Tarka, J.

    2014-12-01

    This paper describes two different optoelectronic detection techniques: cavity-enhanced absorption spectroscopy and photoacoustic spectroscopy. These techniques are designed to perform a sensitive analysis of trace gas species in exhaled human breath for medical applications. With such systems, the detection of pathogenic changes at the molecular level can be achieved. The presence of certain gases (biomarkers), at increased concentration levels, indicates numerous human diseases. Diagnosis of a disease in its early stage would significantly increase chances for effective therapy. Non-invasive, real-time measurements, and high sensitivity and selectivity, capable of minimum discomfort for patients, are the main advantages of human breath analysis. At present, monitoring of volatile biomarkers in breath is commonly useful for diagnostic screening, treatment for specific conditions, therapy monitoring, control of exogenous gases (such as bacterial and poisonous emissions), as well as for analysis of metabolic gases.

  6. Decay Heat Measurements Using Total Absorption Gamma-ray Spectroscopy

    Rice, S.; Valencia, E.; Algora, A.; Taín, J. L.; Regan, P. H.; Podolyák, Z.; Agramunt, J.; Gelletly, W.; Nichols, A. L.

    2012-09-01

    A knowledge of the decay heat emitted by thermal neutron-irradiated nuclear fuel is an important factor in ensuring safe reactor design and operation, spent fuel removal from the core, and subsequent storage prior to and after reprocessing, and waste disposal. Decay heat can be readily calculated from the nuclear decay properties of the fission products, actinides and their decay products as generated within the irradiated fuel. Much of the information comes from experiments performed with HPGe detectors, which often underestimate the beta feeding to states at high excitation energies. This inability to detect high-energy gamma emissions effectively results in the derivation of decay schemes that suffer from the pandemonium effect, although such a serious problem can be avoided through application of total absorption γ-ray spectroscopy (TAS). The beta decay of key radionuclei produced as a consequence of the neutron-induced fission of 235U and 239Pu are being re-assessed by means of this spectroscopic technique. A brief synopsis is given of the Valencia-Surrey (BaF2) TAS detector, and their method of operation, calibration and spectral analysis.

  7. Technical Note: Using a high finesse optical resonator to provide a long light path for differential optical absorption spectroscopy: CE-DOAS

    J. Meinen; J. Thieser; U. Platt; T. Leisner

    2010-01-01

    Cavity enhanced methods in absorption spectroscopy have seen a considerable increase in popularity during the past decade. Especially Cavity Enhanced Absorption Spectroscopy (CEAS) established itself in atmospheric trace gas detection by providing tens of kilometers of effective light path length using a cavity as short as 1 m. In this paper we report on the construction and testing of a compact and power efficient light emitting diode based broadband Cavity Enhanced Differential Optical Abso...

  8. Saturation dynamics and working limits of saturated absorption cavity ringdown spectroscopy.

    Sadiek, Ibrahim; Friedrichs, Gernot

    2016-08-17

    Cavity ringdown spectroscopy (CRDS) in the linear absorption regime is a well-established method for sensitive trace gas detection, but only a few studies have addressed quantitative measurements in the presence of a saturated sample. In fact, saturation is usually avoided in order to escape from the required complex modeling of the saturation process that depends on the characteristics of the absorbing species, its interaction with the surrounding gas as well as on the temporal and spectral characteristics of the cavity excitation. Conversely, the novel saturated-absorption cavity ringdown spectroscopy approach (SCAR/Sat-CRDS) takes advantage of sample saturation in order to allow one to extract both the gas absorption and the empty cavity loss rates from a single ringdown event. Using a new continuous-wave infrared CRD spectrometer equipped with a tunable narrow-bandwidth high-power OPO laser system and a 18 bit digitizer, the transient dynamics of absorption saturation and the working limits of the Sat-CRDS approach in terms of its ability to extract reliable trace gas concentrations have been experimentally studied in this work. Using a strong methane transition as a test case, the excitation power P0 and saturation power PS have been systematically varied to explore a wide range of saturation regimes. At pressures 5 μbar γc, a pronounced coupling between the two parameters has been observed. Finally, a standard error analysis was performed revealing that the Sat-CRDS approach holds its advantages over conventional CRDS implementations in particular when the attainable ultimate detection sensitivity is limited by uncertainties in the empty cavity ringdown constant. PMID:27488884

  9. Nocturnal Measurements of HONO by Differential Optical Absorption Spectroscopy

    Wojtal, P.; McLaren, R.

    2011-12-01

    Differential optical absorption spectroscopy (DOAS) was used to quantify the concentration of HONO, NO2 and SO2 in the nocturnal urban atmosphere at York University over a period of one year. These measurements form a comprehensive HONO data set, including a large range of temperatures, relative humidity, surface conditions (snow, water, dry, etc.) and NO2 concentrations. Laboratory studies and observations within the nocturnal boundary layer reported in the literature suggest heterogeneous conversion of NO2 on surface adsorbed water as the major nighttime source of HONO. HONO formation and photolysis is believed to represent a major source term in the hydroxyl radical budget in polluted continental regions. Currently, most air quality models tend to significantly underpredict HONO, caused by the lack of understanding of HONO formation processes and the parameters that affect its concentration. Recently, we reported nocturnal pseudo steady states (PSS) of HONO in an aqueous marine environment and a conceptual model for HONO formation on aqueous surfaces was proposed. The data set collected at York University is being analyzed with a view towards further understanding the nighttime HONO formation mechanism and testing several hypotheses: 1) A HONO PSS can exist during certain times at night in an urban area in which the HONO concentration is independent of NO2, given the surface contains sufficient water coverage and is saturated with nitrogen containing precursors; 2) The concentration of HONO is positively correlated with temperature during periods where a PSS exists; 3) Different conversion efficiencies of NO2 to HONO exist on dry, wet and snow surfaces; 4) HONO formation has a NO2 order dependence between 0 and 2nd order, dependant on NO2 concentration, relative humidity, etc. The data set will be presented along with statistical analysis that sheds new light on the source of HONO in urban areas at night.

  10. Interferometric measurement of lines shift in flames in connection with interpretation of lined absorption method in atomic absorption spectroscopy

    This paper is concerned with interferometric measuring of the line shift in flames in the view of interpretation of absorption lines in the atomic absorption spectroscopy. The newly measured line shifts were compared to the known data on Lorentz broadening of the same lines obtained by methods free of the systematic errors. The resonant lines of the alkaline earth elements (Sr, Ca, Ba) were investigated. To reduce self-absorption in the flame the solutions with minimum concentrations of the elements were used. The computation scheme includes the spectrometer apparatus width and line broadening due to the self-absorption. Formulae are given for computing the values studied. Good agreement was observed between the computed and experimental results. Error analysis was performed. It was concluded that any line shifts in the hydrocarbons were correctly taken into an account in the absolute computations of absorption

  11. Retrieval of trace gases vertical profile in the lower atmosphere combining. Differential Optical Absorption Spectroscopy with radiative transfer models

    Palazzi, Elisa

    2008-01-01

    The motivation for the work presented in this thesis is to retrieve profile information for the atmospheric trace constituents nitrogen dioxide (NO2) and ozone (O3) in the lower troposphere from remote sensing measurements. The remote sensing technique used, referred to as Multiple AXis Differential Optical Absorption Spectroscopy (MAX-DOAS), is a recent technique that represents a significant advance on the well-established DOAS, especially for what it concerns the study of...

  12. XANES determination of chromium oxidation states in glasses: comparison with optical absorption spectroscopy

    Villain, Olivier; Calas, Georges; Galoisy, Laurence; Cormier, Laurent; Hazemann, Jean-Louis

    2007-01-01

    The oxidation state of chromium in glasses melted in an air atmosphere with and without refining agents was investigated by Cr K-edge X-ray Absorption Near-Edge Structure (XANES) and optical absorption spectroscopy. A good agreement in the relative proportion of Cr(III) and Cr(VI) is obtained between both methods. We show that the chemical dependence of the absorption coefficient of Cr(III) is less important in XANES than in optical absorption spectroscopy. The comparison of glasses melted un...

  13. Identification of Uranyl Minerals Using Oxygen K-Edge X Ray Absorption Spectroscopy

    Ward, Jesse D.; Bowden, Mark E.; Resch, Charles T.; Smith, Steven C.; McNamara, Bruce K.; Buck, Edgar C.; Eiden, Gregory C.; Duffin, Andrew M.

    2016-03-01

    Uranium analysis is consistently needed throughout the fuel cycle, from mining to fuel fabrication to environmental monitoring. Although most of the world’s uranium is immobilized as pitchblende or uraninite, there exists a plethora of secondary uranium minerals, nearly all of which contain the uranyl cation. Analysis of uranyl compounds can provide clues as to a sample’s facility of origin and chemical history. X-ray absorption spectroscopy is one technique that could enhance our ability to identify uranium minerals. Although there is limited chemical information to be gained from the uranium X-ray absorption edges, recent studies have successfully used ligand NEXAFS to study the physical chemistry of various uranium compounds. This study extends the use of ligand NEXAFS to analyze a suite of uranium minerals. We find that major classes of uranyl compounds (carbonate, oxyhydroxide, silicate, and phosphate) exhibit characteristic lineshapes in the oxygen K-edge absorption spectra. As a result, this work establishes a library of reference spectra that can be used to classify unknown uranyl minerals.

  14. Study of self-absorption in laser induced breakdown spectroscopy

    We present a simple analytical expression for self-absorption correction of a spectrum recorded in the image mode of a CCD camera. It is assumed that two spectra are available, F2 recorded with a back mirror and F1 recorded without. The corrected spectrum F0, free of self-absorption, is given by the following simple expression F0=(2F1)/(1+(F2−F1)/(GF1) ) . We discuss the influence of noise on subsequent inverse Abel transform. An example, illustrating proposed method for self-absorption correction and Abel inversion is given in details. - Highlights: • We present a simple expression for self-absorption correction in LIBS plasma. • Method needs two spectra recorded in the image mode of the CCD. • Abel transform is not necessary for self-absorption correction

  15. Femtosecond time-resolved absorption spectroscopy of astaxantin in solution and in alpha-crustacyanin

    Ilagan, R.P.; Christensen, R.L.; Chapp, T.W.; Frank, H.A.; Polívka, Tomáš; Pascher, T.

    2005-01-01

    Roč. 109, č. 14 (2005), s. 3120-3127. ISSN 1089-5639 Institutional research plan: CEZ:AV0Z50510513 Keywords : absorption spectroscopy * astaxantin Subject RIV: BO - Biophysics Impact factor: 2.898, year: 2005

  16. On mechanism of buffer action of La and Sr in atomic absorption spectroscopy

    A possible mechanism is considered for eliminating the effect of a number of macrocomponents on the determination of alkali earth elements with the addition of La and Sr salts. It is shown that the macroelements with the strongest effect in atom absorption flame spectroscopy are the basic elements of rocks. It is established that the effect increases in the order: Fe, Al, Si, i.e., as the crystal chemical radii of the cations decreases. It is suggested that the effect of La, Sr, Ba and other buffer element with large cations very probably leads to an increase in the diffusion coe'ficient of a determined element in less ''dense'' structures than the depressing component which are formed by the buffer element

  17. Concurrent multiaxis differential optical absorption spectroscopy system for the measurement of tropospheric nitrogen dioxide.

    Leigh, Roland J; Corlett, Gary K; Friess, Udo; Monks, Paul S

    2006-10-01

    The development of a new concurrent multiaxis (CMAX) sky viewing spectrometer to monitor rapidly changing urban concentrations of nitrogen dioxide is detailed. The CMAX differential optical absorption spectroscopy (DOAS) technique involves simultaneous spectral imaging of the zenith and off-axis measurements of spatially resolved scattered sunlight. Trace-gas amounts are retrieved from the measured spectra using the established DOAS technique. The potential of the CMAX DOAS technique to derive information on rapidly changing concentrations and the spatial distribution of NO2 in an urban environment is demonstrated. Three example data sets are presented from measurements during 2004 of tropospheric NO2 over Leicester, UK (52.62 degrees N, 1.12 degrees W). The data demonstrate the current capabilities and future potential of the CMAX DOAS method in terms of the ability to measure real-time spatially disaggregated urban NO2. PMID:16983440

  18. Study of near infrared absorption spectroscopy of selected pairs of organic solvents for quality control applications

    Organic solvents of various combinations and ratios, such as ethanol/commercial petrol; benzene/ethanol; toluene/commercial petrol and toluene/benzene were studied by near infrared (NIR) absorption spectroscopy. NIR spectrometer of 850-1700 nm produced distinctly separable spectral ranges for all the combinations; 1400 to 1650 nm for ethanol/commercial petrol; 1125 to 1150 nm for benzene/ethanol; 1130 to 1150 nm for toluene/commercial petrol and 1175 to 1210 nm for toluene/benzene. The calibration curves were drawn for the given pair concentrations. From the linear fitting parameters it is evident that each pair has different slope, which establishes reliability of the technique. The results revealed that each solvent in the mixture gives a clear trend of spectral region. This may be used for the analysis of mixtures of organic solvents. The technique may be utilized for the quality assurance. (author)

  19. Utilization of synchrotron radiation in analytical chemistry. Soft X-ray emission and absorption spectroscopy

    Synchrotron soft X-ray spectroscopy includes three major types of spectroscopy such as X-ray absorption spectroscopy (XAS), X-ray emission spectroscopy (XES), and X-ray photoelectron spectroscopy (XPS). This paper takes up XAS and XES of soft X-rays, and briefly describes the principle. XAS is roughly classified into XANES (X-ray absorption near-edge structure) and EXAFS (extended X-ray absorption fine structure), and XANES is mainly used in the analysis based on XAS of soft X-rays. As the examples of the latest soft X-ray analyses, the following are introduced: (1) bandgap of boron implantation diamond and the local structure of boron, (2) catalytic sites in solid fuel cell carbon electrode, and (3) soft X-ray analysis under atmospheric pressure. (A.O.)

  20. In situ gas temperature measurements by UV-absorption spectroscopy

    Fateev, Alexander; Clausen, Sønnik

    2009-01-01

    range from 23 degrees C to 1,500 degrees C. The gas temperature was evaluated (1) from the analysis of the structure of selected NO high-resolution gamma-absorption bands and (2) from the analysis of vibrational distribution in the NO gamma-absorption system in the (211-238) nm spectral range. The......The absorption spectrum of the NO A(2)Sigma(+) <- X(2)Pi gamma-system can be used for in situ evaluation of gas temperature. Experiments were performed with a newly developed atmospheric-pressure high-temperature flow gas cell at highly uniform and stable gas temperatures over a 0.533 m path in the...... accuracy of both methods is discussed. Validation of the classical Lambert-Beer law has been demonstrated at NO concentrations up to 500 ppm and gas temperatures up to 1,500 degrees C over an optical absorption path length of 0.533 m....

  1. Multiple scattering approach to X-ray absorption spectroscopy

    2003-01-01

    In this paper we present the state of the art of the theoretical background needed for analyzing X-ray absorption spectra in the whole energy range. The multiple-scattering (MS) theory is presented in detail with some applications on real systems. We also describe recent progress in performing geometrical fitting of the XANES (X-ray absorption near-edge structure) energy region and beyond using a full multiple-scattering approach.

  2. Two-wavelength absorption modulation spectroscopy of bandtail absorption in GaAs quantum wells

    We have discovered that below-band-gap photoexcitation produces large bleaching of the exciton absorption in GaAs quantum well heterostructures. We have used this effect to perform the first investigation of room-temperature bandtail absorption in these structures. We find that the below-band-gap absorption follows a spectral Urbach's rule. In addition, proton-bombarded samples show an Urbach energy correlated with bombardment-induced defects. This sensitive technique has enabled us to study samples as thin as 1 μm at energies where the absorption coefficient is approx.10 cm-1

  3. Ultrafast terahertz conductivity and transient optical absorption spectroscopy of silicon nanocrystal thin films

    Titova, Lyubov V.; Harthy, Rahma Al; Cooke, David;

    We use time-resolved THz spectroscopy and transient optical absorption spectroscopy as two complementary techniques to study ultrafast carrier dynamics in silicon nanocrystal thin films. We find that the photoconductive dynamics in these materials is dominated by interface trapping, and we observe...

  4. Trace gas absorption spectroscopy using laser difference-frequency spectrometer for environmental application

    Chen, W.; Cazier, F.; Boucher, D.; Tittel, F. K.; Davies, P. B.

    2001-01-01

    A widely tunable infrared spectrometer based on difference frequency generation (DFG) has been developed for organic trace gas detection by laser absorption spectroscopy. On-line measurements of concentration of various hydrocarbons, such as acetylene, benzene, and ethylene, were investigated using high-resolution DFG trace gas spectroscopy for highly sensitive detection.

  5. Ultrafast X-ray absorption spectroscopy of laser-excited materials

    Advanced Light Source (ALS) Beamline 6.0 is designed for x-ray absorption spectroscopy with femtosecond x-ray pulse generated by bunch 'slicing' technique. Soft and hard x-ray branch lines will cover a wide photon energy range from 120 eV to 10 KeV. A soft x-ray spectrograph will collect absorption spectra dispersively. The application of laminar gratings to dispersive x-ray absorption spectroscopy in the photon energy range 2-8 KeV has been investigated. (author)

  6. Theoretical experimental study of the factors that govern the molybdenum absorption signal by means of electro thermic atomic absorption spectroscopy

    The formation of molybdenum carbides in the atomizer, used in the electro thermic atomic absorption spectroscopy, is responsible for incomplete analyte removal in its analysis. This generates the apparition of the memory effect and little precision in the results. In this work, different variables that could affect the molybdenum absorption sign were investigated, as well as the influence of hydrochloric acid on the memory effect, by means of studies in the different stages: drying, calcination and atomization, and the samples deposition order in molybdenum solutions, either acidified or not acidified

  7. [The Research for Trace Ammonia Escape Monitoring System Based on Tunable Diode Laser Absorption Spectroscopy].

    Zhang, Li-fang; Wang, Fei; Yu, Li-bin; Yan, Jian-hua; Cen, Ke-fa

    2015-06-01

    In order to on-line measure the trace ammonia slip of the commercial power plant in the future, this research seeks to measure the trace ammonia by using tunable diode laser absorption spectroscopy under ambient temperature and pressure, and at different temperatures, and the measuring temperature is about 650 K in the power plant. In recent years lasers have become commercially available in the near-infrared where the transitions are much stronger, and ammonia's spectroscopy is pretty complicated and the overlapping lines are difficult to resolve. A group of ammonia transitions near 4 433.5 cm(-1) in the v2 +v3 combination band have been thoroughly selected for detecting lower concentration by analyzing its absorption characteristic and considering other absorption interference in combustion gases where H2O and CO2 mole fraction are very large. To illustrate the potential for NH3 concentration measurements, predictions for NH3, H2O and CO2 are simultaneously simulated, NH3 absorption lines near 4 433.5 cm(-1) wavelength meet weaker H2O absorption than the commercial NH3 lines, and there is almost no CO2 absorption, all the parameters are based on the HITRAN database, and an improved detection limit was obtained for interference-free NH3 monitoring, this 2.25 μm band has line strengths several times larger than absorption lines in the 1.53 μm band which was often used by NH3 sensors for emission monitoring and analyzing. The measurement system was developed with a new Herriott cell and a heated gas cell realizing fast absorption measurements of high resolution, and combined with direct absorption and wavelenguh modulation based on tunable diode laser absorption spectroscopy at different temperatures. The lorentzian line shape is dominant at ambient temperature and pressure, and the estimated detectivity is approximately 0.225 x 10(-6) (SNR = 1) for the directed absorption spectroscopy, assuming a noise-equivalent absorbance of 1 x 10(-4). The heated cell

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

    de Groot, F. M. F.

    2001-01-01

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

  9. Quantifying the Aggregation Factor in Carbon Nano tube Dispersions by Absorption Spectroscopy

    Absorption spectroscopy in the ultraviolet-visible-near infrared (UV-Vis-NIR) wavelength region has been used to quantify the aggregation factor of single-walled carbon nano tubes (SWCNTs) in liquid media through a series of controlled experiments. SWCNT bundles are dispersed in selected solvents using a calibrated ultrasonicator, which helps in determining the true amount of energy used in the exfoliation process. We also establish the selectivity of the centrifugation process, under the conditions used, in removing the nano tube aggregates as a function of the sonication time and the dispersion solvent. This study, along with the calibration of the sonication process, is shown to be very important for measuring the true aggregation factor of SWCNTs through a modified approach. We also show that the systematic characterization of SWCNT dispersions by optical spectroscopy significantly contributes to the success of di electrophoresis (DEP) of nano tubes at predefined on-chip positions. The presence of individually dispersed SWCNTs in the dispersions is substantiated by di electrophoretic assembly and post-DEP electromechanical measurements.

  10. Absorption spectroscopy of electronic states near Fermi level

    This paper reports that the temperature behavior of the absorption spectra of superconducting YBa2-Cu3-O7-δ textured films is measured in a 1.5 + 3.0 eV energy region with varying temperatures from 25 to 300 K. The spectra are found to be sensitive to a superconducting transition: the temperature-dependent behavior of absorption at T > Tc undergoes critical changes under the superconducting transition and for T c the spectrum ceases to depend on temperature. The spectra display an exciton maximum in the optical gap Eg = 1.95 eV. The spectrum freezing at Tc can be explained assuming that the Fermi level is in temperature resonance with a narrow local level which is responsible for a delta-like singularity in the density of states

  11. A heated chamber burner for atomic absorption spectroscopy.

    Venghiattis, A A

    1968-07-01

    A new heated chamber burner is described. The burner is of the premixed type, and burner heads of the types conventionally used in atomic absorption may be readily adapted to it. This new sampling system has been tested for Ag, Al, Ca, Cu, Fe, Mg, Mn, Ni, Pb, Si, Ti, and Zn in aqueous solutions. An improvement of the order of ten times has been obtained in sensitivity, and in detection limits as well, for the elements determined. Interferences controllable are somewhat more severe than in conventional burners but are controllable. PMID:20068792

  12. [Retrieval of tropospheric NO2 by multi axis differential optical absorption spectroscopy].

    Xu, Jin; Xie, Pin-hua; Si, Fu-qi; Dou, Ke; Li, Ang; Liu, Yu; Liu, Wen-qing

    2010-09-01

    A method of retrieving NO2 in troposphere based on multi axis differential optical absorption spectroscopy (MAX-DOAS) was introduced. The differential slant column density (dSCD) of NO2 was evaluated by differential optical absorption spectroscopy (DOAS), removing the Fraunhofer structure and Ring effect. Combining the results of different observing directions, the tropospheric NO2 differential slant column density (deltaSCD) was evaluated, and the air mass factor (AMF) was calculated with the radiative transfer model SCIATRAN and the tropospheric NO2 vertical column density (VCD) was retrieved. To ensure the accuracy of the results, it was compared with the results of long path differential optical absorption spectroscopy (LP-DOAS), a good accordance was shown with the correlation coefficients of 0.94027 and 0.96924. PMID:21105419

  13. Surface and ultrathin-layer absorptance spectroscopy for solar cells

    Holovský, Jakub; Remeš, Zdeněk; De Wolf, S.; Ballif, C.

    Vol. 60. Amsterdam: Elsevier Ltd, 2014 - (Gordon, I.; Valenta, J.; Turan, R.; Atwater, H.; Mirabella, S.), s. 57-62 ISSN 1876-6102. [E- MRS Spring Meeting 2014. Lille (FR), 26.05.2014-30.05.2014] R&D Projects: GA MŠk 7E12029; GA ČR(CZ) GA14-05053S EU Projects: European Commission(XE) 283501 - FAST TRACK Institutional support: RVO:68378271 Keywords : surface states * thin-film limit * ATR-FTIR * photothermal deflection spectrscopy * photocurrent spectroscopy Subject RIV: BM - Solid Matter Physics ; Magnetism

  14. Polarization dependent interface properties of ferroelectric Schottky barriers studied by soft X-ray absorption spectroscopy

    Kohlstedt, H.; Petraru, A.; Denlinger, M. Meier J.; Guo, J.; Wanli, Y.; A. Scholl; Freelon, B.; Schneller, T.; Waser, R.; Yu, P; Ramesh, R.; Learmonth, T.; Glans, P.-A.; Smith, K. E.

    2008-01-01

    We applied soft X-ray absorption spectroscopy to study the Ti L-edge in ferroelectric capacitors using a modified total electron yield method. The inner photo currents and the X-ray absorption spectra were polarization state dependent. The results are explained on the basis of photo electric effects and the inner potential in the ferroelectric capacitors as a result of back-to-back Schottky barriers superimposed by the potential due to the depolarization field. In general, the presented metho...

  15. Optical-Feedback Cavity-Enhanced Absorption Spectroscopy with a Quantum Cascade Laser.

    Maisons, G.; Gorrotxategi Carbajo, P.; Carras, M.; Romanini, D.

    2010-01-01

    Optical{feedback cavity{enhanced absorption spectroscopy is demonstrated in the mid{IR using a quantum cascade laser (emitting at 4.46 ¹m). The laser linewidth reduction and frequency locking by selective optical feedback from the resonant cavity ¯eld turns out to be particularly important in this spectral range: It allows strong cavity transmission which compensates for low light sensitivity, especially when using room temperature detectors. We obtain a noise equivalent absorption coe±cient ...

  16. Broadband Cavity Enhanced Differential Optical Absorption Spectroscopy (CE-DOAS) – applicability and corrections

    U. Platt; J. Meinen; D. Pöhler; T. Leisner

    2008-01-01

    Atmospheric trace gas measurements by cavity assisted long-path absorption spectroscopy are an emerging technology. An interesting approach is the combination of CEAS with broadband light sources, the broadband CEAS (BB-CEAS). BB-CEAS lends itself to the application of the DOAS technique to analyse the derived absorption spectra. While the DOAS approach has enormous advantages in terms of sensitivity and specificity of the measurement, an important implication is the reduction of the light pa...

  17. Alternative method for concentration retrieval in differential optical absorption spectroscopy atmospheric gas pollutant measurements

    Videla, Fabián; Schinca, Daniel Carlos; Tocho, Jorge O.

    2003-01-01

    Differential optical absorption spectroscopy is a widely used technique for open-column atmospheric-gas pollution monitoring. The concentration retrieval is based on the fitting of the measured differential absorbance through the Lambert-Beer law. We present an alternative method for calculating the gas concentration on the basis of the proportionality between differential absorbance and differential absorption cross section of the gas under study. The method can be used on its own for single...

  18. Absorption spectroscopy in the ultraviolet and visible spectral range of hexavalent chromium aqueous solutions

    Mignani, Anna G.; Spadoni, Lorenzo

    1999-09-01

    In order to demonstrate the possibility of performing direct absorption spectroscopy of Hexavalent Chromium aqueous solutions, absorption measurements were performed at the dual- beam spectrophotometer in the 250 - 850 nm spectral range, with 10 mm and 100 mm path lengths. Low concentration (26 - 520 (mu) g/l) (and high concentration (2.6 - 52 mg/l) solutions were analyzed, showing that it is possible to implement a basic instrumentation for risk condition monitoring and a more advanced instrumentation for quantitative measurements.

  19. Non-intrusive sensing of air velocity, humidity, and temperature using tunable diode laser absorption spectroscopy

    Park, Suhyeon

    2015-01-01

    This work will report the non-intrusive sensing of air velocity, humidity, and temperature using tunable diode laser absorption spectroscopy (TDLAS), and discuss the potential applications of such sensors for in situ monitoring and active control for wind energy. The sensing technique utilizes the absorption features of water vapor in ambient air to monitor multiple flow parameters including velocity, humidity, and temperature simultaneously and non-intrusively [1-3]. The TDLAS technique does...

  20. Total absorption spectroscopy of N = 51 nucleus 85Se

    Goetz, K. C.; Grzywacz, R. K.; Rykaczewski, K. P.; Karny, M.; Fialkowska, A.; Wolinska-Cichocka, M.; Rasco, B. C.; Zganjar, E. F.; Johnson, J. W.; Gross, C. J.

    2014-09-01

    An experimental campaign utilizing the Modular Total Absorption Spectrometer (MTAS) was conducted at the HRIBF facility in January of 2012. The campaign studied 22 isotopes, many of which were identified as the highest priority for decay heat analysis during a nuclear fuel cycle, see the report by the OECD-IAEA Nuclear Energy Agency in 2007. The case of 85Se will be discussed. 85Se is a Z = 34, N = 51 nucleus with the valence neutron located in the positive parity sd single particle state. Therefore, its decay properties are determined by interplay between first forbidden decays of the valence neutron and Gamow-Teller decay of a 78Ni core. Analysis of the data obtained during the January 2012 run indicates a significant increase of the beta strength function when compared with previous measurements, see Ref..

  1. Thyroid lesions diagnosis by Fourier transformed infrared absorption spectroscopy (FTIR)

    Thyroid nodules are a common disorder, with 4-7% of incidence in the Brazilian population. Although the fine needle aspiration (FNA) is an accurate method for thyroid tumors diagnosis, the discrimination between benign and malignant neoplasm is currently not possible in some cases with high incidence of false negative diagnosis, leading to a surgical intervention due to the risk of carcinomas. The aim of this study was to verify if the Fourier Transform infrared spectroscopy (FTIR) can contribute to the diagnosis of thyroid carcinomas and goiters, using samples of tissue and aspirates. Samples of FNA, homogenates and tissues of thyroid nodules with histopathological diagnosis were obtained and prepared for FTIR spectroscopy analysis. The FNA and homogenates samples were measured by μ-FTIR (between 950 . 1750 cm-1), at a nominal resolution of 4 cm-1 and 120 scans). Tissue samples were analyzed directly by ATR-FTIR technique, at a resolution 2 cm-1, with 60 scans in the same region. All spectra were corrected by the baseline and normalized by amides area (1550-1640 cm-1) in order to minimize variations of sample homogeneity. Then, spectra were converted into second derivatives using the Savitzk-Golay algorithm with a 13 points window. The Ward's minimum variance algorithm and Euclidean distances among the points were used for cluster analysis. Some FNA samples showed complex spectral pattern. All samples showed some cell pellets and large amount of hormone, represented by the bands of 1545 and 1655 cm-1. Bands in 1409, 1412, 1414, 1578 and 1579 cm-1 were also found, indicating possible presence of sugar, DNA, citric acid or metabolic products. In this study, it was obtained an excellent separation between goiter and malign lesion for the samples of tissues, with 100% of specificity in specific cluster and 67% sensibility and 50 of specificity. In homogenate and FNA samples this sensibility and specificity were lower, because among these samples, it were included

  2. Absorption spectroscopy of powdered materials using time-resolved diffuse optical methods.

    D'Andrea, Cosimo; Obraztsova, Ekaterina A; Farina, Andrea; Taroni, Paola; Lanzani, Guglielmo; Pifferi, Antonio

    2012-11-10

    In this paper a novel method, based on time-resolved diffuse optical spectroscopy, is proposed to measure the absorption of small amounts of nanostructured powder materials independent of scattering. Experimental validation, in the visible and near-infrared spectral range, has been carried out on India Inkparticles. The effectiveness of the technique to measure scattering-free absorption is demonstrated on carbon nanotubes. The comparison between the absorption spectra acquired by the proposed method and conventional measurements performed with a commercial spectrophotometer is discussed. PMID:23142900

  3. Quartz crystal microbalance and infrared reflection absorption spectroscopy characterization of bisphenol A absorption in the poly(acrylate) thin films.

    Li, Guifeng; Morita, Shigeaki; Ye, Shen; Tanaka, Masaru; Osawa, Masatoshi

    2004-02-01

    The absorption process of bisphenol A (BPA) in a number of poly(acrylate) thin films, such as poly(2-methoxyethyl acrylate) (PMEA), poly(ethyl acrylate) (PEA), poly(n-butyl methacrylate) (PBMA), and poly(methyl methacrylate) (PMMA), has been investigated by quartz crystal microbalance (QCM) and infrared reflection absorption spectroscopy (IRRAS) measurements. Both QCM and IRRAS measurements show that the BPA molecules absorb in PMEA, PEA, and PBMA thin films but not in PMMA thin film. The differences in the BPA absorption behavior are mainly attributed to the difference in the glass transition temperature (T(g)) between these polymers. This absorption behavior also depends on the BPA concentration and polymer film thickness. Furthermore, IRRAS characterization demonstrates that the hydrogen bonding is formed between the hydroxyl group in BPA and the carbonyl group in the poly(acrylate) thin films. BPA molecule absorbed in these polymer thin films can be removed by ethanol rinse treatment. By optimizing experimental conditions for the QCM electrode modified by PMEA thin film, detection limitation of approximately 1 ppb for BPA can be realized by the in situ QCM measurement. This method is expected to be a sensitive in situ detection way for trace BPA in the environmental study. PMID:14750877

  4. Determination of atmospheric corrosion of coated steel surfaces by in situ infrared reflection absorption spectroscopy (IRRAS)

    Full text: Infrared reflection absorption spectroscopy (IRRAS) is a sensitive technique for measuring thin layers on metallic surfaces. The principal goal of this IRRAS study was the development of a reproducible and reliable in situ measurement procedure for the determination of corrosion of coated steel surfaces. (author)

  5. Absorption and Scattering Coefficients: A Biophysical-Chemistry Experiment Using Reflectance Spectroscopy

    Cordon, Gabriela B.; Lagorio, M. Gabriela

    2007-01-01

    A biophysical-chemistry experiment, based on the reflectance spectroscopy for calculating the absorption and scattering coefficients of leaves is described. The results show that different plants species exhibit different values for both the coefficients because of their different pigment composition.

  6. Absorption spectroscopy of Al XIII Ly-ŕ radiation by an Fe XXIV plasma

    Gouveia, A.; Al'miev, I. R.; Hawreliak, J.; Chambers, D. M.; Liang, T.; Marjoribanks, R.; Pinto, O.; Renner, Oldřich; Zhang, J.; Wark, J. S.

    2003-01-01

    Roč. 81, - (2003), s. 199-207. ISSN 0022-4073 Institutional research plan: CEZ:AV0Z1010921 Keywords : XUV laser * radiative transfer * X-ray absorption spectroscopy Subject RIV: BL - Plasma and Gas Discharge Physics Impact factor: 1.382, year: 2003

  7. Study of cancer cell lines with Fourier transform infrared (FTIR)/vibrational absorption (VA) spectroscopy

    Uceda Otero, E. P.; Eliel, G. S. N.; Fonseca, E. J. S.;

    2013-01-01

    In this work we have used Fourier transform infrared (FTIR) / vibrational absorption (VA) spectroscopy to study two cancer cell lines: the Henrietta Lacks (HeLa) human cervix carcinoma and 5637 human bladder carcinoma cell lines. Our goal is to experimentally investigate biochemical changes and d...

  8. Oxidation of plutonium dioxide: an X-ray absorption spectroscopy study

    X-ray absorption spectroscopy experiments were conducted in order to characterise plutonium dioxide oxidation. It is shown that the sample preparation adopted does not enable elaboration of hyperstoichiometric plutonium dioxide. These results could mean that plutonium dioxide oxidation only occurs under very specific conditions

  9. Gas concentration measurement by optical similitude absorption spectroscopy: methodology and experimental demonstration.

    Anselmo, Christophe; Welschinger, Jean-Yves; Cariou, Jean-Pierre; Miffre, Alain; Rairoux, Patrick

    2016-06-13

    We propose a new methodology to measure gas concentration by light-absorption spectroscopy when the light source spectrum is larger than the spectral width of one or several molecular gas absorption lines. We named it optical similitude absorption spectroscopy (OSAS), as the gas concentration is derived from a similitude between the light source and the target gas spectra. The main OSAS-novelty lies in the development of a robust inversion methodology, based on the Newton-Raphson algorithm, which allows retrieving the target gas concentration from spectrally-integrated differential light-absorption measurements. As a proof, OSAS is applied in laboratory to the 2ν3 methane absorption band at 1.66 µm with uncertainties revealed by the Allan variance. OSAS has also been applied to non-dispersive infra-red and the optical correlation spectroscopy arrangements. This all-optics gas concentration retrieval does not require the use of a gas calibration cell and opens new tracks to atmospheric gas pollution and greenhouse gases sources monitoring. PMID:27410280

  10. Spectroscopy

    Hellman, Hal

    1968-01-01

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

  11. Silicon oxide particle formation in RF plasmas investigated by infrared absorption spectroscopy and mass spectrometry

    In situ Fourier transform infrared absorption spectroscopy has been used to study the composition of particles formed and suspended in radio-frequency discharges of silane-oxygen-argon gas mixtures. The silane gas consumption was observed by infrared absorption. The stoichiometry of the produced particles depends on the silane flow rate and was compared with commercial colloidal silica. A small proportion of silane gas produces nanometric stoichiometric particles whereas a large proportion produces larger under-stoichiometric particles. Absorption spectroscopy was sufficiently sensitive to reveal particles too small to be visually observed by laser light scattering. Post-oxidation of hydrogenated silicon particles trapped in an argon plasma by adding oxygen was demonstrated. Mass spectrometry of negative and positive ions showed an extensive range of ionic clusters which may be at the origin of particle formation. A model based on an iterative reaction sequence gives a good agreement with the measured positive ion mass spectrum. (author) 7 figs., 1 tab., 34 refs

  12. Incoherent broadband cavity enhanced absorption spectroscopy using supercontinuum and superluminescent diode sources.

    Aalto, Antti; Genty, Goëry; Laurila, Toni; Toivonen, Juha

    2015-09-21

    We investigate incoherent broadband cavity enhanced absorption spectroscopy using a tailored supercontinuum source. By tailoring the supercontinuum spectrum to match the high reflectivity bandwidth of the mirrors, we achieve an unprecedented spectral brightness of more than 7 dBm/nm at wavelengths where the effective absorption path length in the cavity exceeds 40 km. We demonstrate the potential of the source in spectrally broadband measurement of weak overtone transitions of carbon dioxide and methane in the near-infrared 1590 nm - 1700 nm range and evaluate its performance against that of a typical superluminescent diode source. Minimum detectable absorption coefficients (3σ) of 2.2 × 10(-9) cm(-1) and 6.2 × 10(-9) cm(-1) are obtained with the supercontinuum and the superluminescent diode sources, respectively. We further develop a spectral fitting method based on differential optical absorption spectroscopy to fully and properly account for the combined effect of absorption line saturation and limited spectral resolution of the detection. The method allows to cope with high dynamic range of absorption features typical of real-world multi-component measurements. PMID:26406720

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

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

    2013-11-01

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

  14. Development and application of UV-visible and mid-IR differential absorption spectroscopy techniques for pollutant trace gas monitoring

    Jiménez Pizarro, Rodrigo; Calpini, Bertrand

    2005-01-01

    Spatial representativeness is an important quality criterion in trace gas monitoring, especially if measurements are intended for regulatory and model validation purposes. Open-path absorption spectroscopy techniques meet the representativeness requirement by providing concentrations averaged over atmospheric paths ranging from some hundred meters to some kilometers. This research concerns the characterization and application of a UV-visible differential optical absorption spectroscopy (DOAS)...

  15. Development and application of UV-visible and mid-IR differential absorption spectroscopy techniques for pollutant trace gas monitoring

    Jiménez Pizarro, Rodrigo

    2004-01-01

    Spatial representativeness is an important quality criterion in trace gas monitoring, especially if measurements are intended for regulatory and model validation purposes. Open-path absorption spectroscopy techniques meet the representativeness requirement by providing concentrations averaged over atmospheric paths ranging from some hundred meters to some kilometers. This research concerns the characterization and application of a UV-visible differential optical absorption spectroscopy (DOAS)...

  16. Picosecond absorption spectroscopy of an intense ultrafast laser produced plasma; Spectroscopie d'absorption picoseconde d'un plasma produit par un laser intense ultra bref

    Renaudin, P.; Gary, S. [CEA Bruyeres-le-Chatel, 91 (France); Audebert, P.; Bastiani-Ceccotti, S.; Chenais-Popovics, C.; Geindre, J.P. [Laboratoire pour l' Utilisation des Lasers Intenses (LULI), Unite Mixte de recherche n. 7605 CNRS - CEA - Ecole Polytechnique - Universite Pierre et Marie Curie (France); Gauthier, J.C. [Le Centre Laser Intense et application (CELIA) est une unite mixte de recherche CNRS-CEA-UB1, 33 - Talence (France); Shepherd, R. [Lawrence Livermore National Lab., CA (United States)

    2008-11-15

    By using high-intensity sub-picosecond lasers, it is possible to heat a solid up to million degrees with very shallow gradients. We present an experiment where a thin foil is irradiated by a sub-picosecond laser. Frequency domain interferometry measures the velocity of the rear critical density using a pomp-probe method. The recombination dynamics of the transient plasma is measured by point-projection absorption spectroscopy. The good agreement between the experimental data, atomic physics calculations, and hydrodynamic modelling demonstrates the capability of the codes to reproduce the ultra fast evolution of plasmas in the sub-picosecond regime. (authors)

  17. High sensitivity ultra-broad-band absorption spectroscopy of inductively coupled chlorine plasma

    Marinov, Daniil; Foucher, Mickaël; Campbell, Ewen; Brouard, Mark; Chabert, Pascal; Booth, Jean-Paul

    2016-06-01

    We propose a method to measure the densities of vibrationally excited Cl2(v) molecules in levels up to v  =  3 in pure chlorine inductively coupled plasmas (ICPs). The absorption continuum of Cl2 in the 250–450 nm spectral range is deconvoluted into the individual components originating from the different vibrational levels of the ground state, using a set of ab initio absorption cross sections. It is shown that gas heating at constant pressure is the major depletion mechanism of the Cl2 feedstock in the plasma. In these line-integrated absorption measurements, the absorption by the hot (and therefore rarefied) Cl2 gas in the reactor centre is masked by the cooler (and therefore denser) Cl2 near the walls. These radial gradients in temperature and density make it difficult to assess the degree of vibrational excitation in the centre of the reactor. The observed line-averaged vibrational distributions, when analyzed taking into account the radial temperature gradient, suggest that vibrational and translational degrees of freedom in the plasma are close to local equilibrium. This can be explained by efficient vibrational-translational (VT) relaxation between Cl2 and Cl atoms. Besides the Cl2(v) absorption band, a weak continuum absorption is observed at shorter wavelengths, and is attributed to photodetachment of Cl‑ negative ions. Thus, line-integrated densities of negative ions in chlorine plasmas can be directly measured using broad-band absorption spectroscopy.

  18. Infrared-laser spectroscopy using a long-pathlength absorption cell

    The absorption measurements in an ordinary cell may require typically a few torr pressure of sample gas. At these pressures the absorption lines are usually pressure-broadened and, therefore, closely spaced transitions are poorly resolved even at diode-laser resolution. This situation is greatly improved in Doppler-limited spectroscopy at extremely low sample pressures. Two very long-pathlength absorption cells were developed to be used in conjunction with diode lasers. They were designed to operate at controlled temperatures with the optical pathlength variable up to approx. 1.5 km. Not only very low sample pressures are used for studies with such cells but also the spectroscopic sensitivity is enhanced over conventional methods by a factor of 103 to 104, improving the analytical capability of measuring particle densities to the order of 1 x 10'' molecules/cm3. This paper presents some analytical aspects of the diode laser spectroscopy using the long-pathlength absorption cells in the areas of absorption line widths, pressure broadening coefficients, isotope composition measurements and trace impurity analysis

  19. Hydrogenated carbon nanotubes: x-ray absorption spectroscopy and ab initio simulation analysis

    The paper presents the results of investigation of the chemical bond formation in hydrogenated single-walled carbon nanotubes using X-ray absorption spectroscopy. All measurements were performed with the use of synchrotron radiation at BESSY II. The C1s absorption spectra point to formation of covalent chemical bonding between the hydrogen and carbon atoms in H-SWNTs. The investigation of the H-SWNT local structure has been carried out on the basis of the semi-empirical PM6 method (MOPAC 2009) and Finite Difference method. The possibility of H-SWNTs dehydrogenation was also investigated.

  20. Characterization of Metalloproteins and Biomaterials by X-ray Absorption Spectroscopy and X-ray Diffraction

    Frankær, Christian Grundahl

    and R6) were solved by single crystal X-ray diffraction (XRD) to 1.40 Å, 1.30 Å and 1.80 Å resolution, respectively. The zinc coordination in each conformation was studied by XAS including both extended X-ray absorption fine structure (EXAFS) spectroscopy and X-ray absorption near edge structure...... the zinc coordination in the T3-sites, in particular. Furthermore, XANES spectra for the zinc sites in T6 and R6 insulin were successfully calculated using finite difference methods, and the bond distances and angles were optimized from a quantitative XANES analysis. T6 insulin was furthermore...

  1. Linear cavity optical-feedback cavity-enhanced absorption spectroscopy with a quantum cascade laser.

    Bergin, A G V; Hancock, G; Ritchie, G A D; Weidmann, D

    2013-07-15

    A cw distributed feedback quantum cascade laser (DFB-QCL) coupled to a two-mirror linear optical cavity has been used to successfully demonstrate optical-feedback cavity-enhanced absorption spectroscopy (OF-CEAS) at 5.5 μm. The noise-equivalent absorption coefficient, α(min), was 2.4×10(-8) cm(-1) for 1 s averaging, limited by etalon-fringing. The temporal stability of the instrument allows NO detection down to 5 ppb in 2 s. PMID:23939085

  2. NO2 measurements in Hong Kong using LED based long path differential optical absorption spectroscopy

    Chan, K. L.; Pöhler, D.; G. Kuhlmann; Hartl, A.; Platt, U.; M. O. Wenig

    2012-01-01

    In this study we present the first long term measurements of atmospheric nitrogen dioxide (NO2) using a LED based Long Path Differential Optical Absorption Spectroscopy (LP-DOAS) instrument. This instrument is measuring continuously in Hong Kong since December 2009, first in a setup with a 550 m absorption path and then with a 3820 m path at about 30 m to 50 m above street level. The instrument is using a high power blue light LED with peak intensity at 450 nm coupled into t...

  3. Precise shear waves absorption measurements by the Elasto-Magnetic Resonance Spectroscopy method

    Klinkosz, T

    2003-01-01

    The essential feature of the method is the employment of elasto-magnetic resonance spectroscopy (EMRS) for precise measurement of the absorption of transverse elastic waves introduced into a biological sample. Such a measurement can be accomplished by combining the EMRS method with such methods, in which collective dislocations of spins are induced by external physical factors, e.g. variable electric field, strong magnetic field gradient or longitudinal elastic wave. This has been illustrated herein on the example of Electrical Mobility Magnetic Resonance Spectroscopy (EMMRS).

  4. Capturing molecular structural dynamics by 100 ps time-resolved X-ray absorption spectroscopy

    An experimental set-up for time-resolved X-ray absorption spectroscopy with 100 ps time resolution at beamline NW14A at the Photon Factory Advanced Ring is presented. An experimental set-up for time-resolved X-ray absorption spectroscopy with 100 ps time resolution at beamline NW14A at the Photon Factory Advanced Ring is presented. The X-ray positional active feedback to crystals in a monochromator combined with a figure-of-merit scan of the laser beam position has been utilized as an essential tool to stabilize the spatial overlap of the X-ray and laser beams at the sample position. As a typical example, a time-resolved XAFS measurement of a photo-induced spin crossover reaction of the tris(1,10-phenanthrorine)iron(II) complex in water is presented

  5. Diagnosis of laser ablated carbon particles measured by time-resolved X-ray absorption spectroscopy

    The time and space resolved properties of laser ablated carbon particles were measured by X-ray absorption spectroscopy using LPX as an X-ray source. The energy density of the irradiation laser on the sample was in the range of 0.5-20J/cm2 and the time delay was varied between 0 and 120ns. The absorption spectra exhibited several peaks originated from level to level transitions and an intense broad absorption in the energy range of C-K edge. At a delay time of 120ns, the absorption peak from 1s→2p transition of neutral carbon atom (C0), C-, C+ and C2+ ions were observed. The absorption peak from C0 was stronger as the probing position was closer to the sample surface and decreased rapidly with distance from the sample surface. The absorption peak C2+ ion was observed only at comparatively distant positions from surface. The maximum speeds of highly charged ions were faster than that of neutral atoms and negative charged ions. The neutral atom and lower charged ions were emitted from the sample even after laser irradiation. The spatial distributions of the laser ablated carbon particles in the localized helium gas environment were measured. In the helium gas environment, the ablation plume was depressed by the helium cloud generated on the top of ablation plume. (author)

  6. Undistorted X-ray Absorption Spectroscopy Using s-Core-Orbital Emissions.

    Golnak, Ronny; Xiao, Jie; Atak, Kaan; Unger, Isaak; Seidel, Robert; Winter, Bernd; Aziz, Emad F

    2016-05-12

    Detection of secondary emissions, fluorescence yield (FY), or electron yield (EY), originating from the relaxation processes upon X-ray resonant absorption has been widely adopted for X-ray absorption spectroscopy (XAS) measurements when the primary absorption process cannot be probed directly in transmission mode. Various spectral distortion effects inherent in the relaxation processes and in the subsequent transportation of emitted particles (electron or photon) through the sample, however, undermine the proportionality of the emission signals to the X-ray absorption coefficient. In the present study, multiple radiative (FY) and nonradiative (EY) decay channels have been experimentally investigated on a model system, FeCl3 aqueous solution, at the excitation energy of the Fe L-edge. The systematic comparisons between the experimental spectra taken from various decay channels, as well as the comparison with the theoretically simulated Fe L-edge XA spectrum that involves only the absorption process, indicate that the detection of the Fe 3s → 2p partial fluorescence yield (PFY) gives rise to the true Fe L-edge XA spectrum. The two key characteristics generalized from this particular decay channel-zero orbital angular momentum (i.e., s orbital) and core-level emission-set a guideline for obtaining undistorted X-ray absorption spectra in the future. PMID:27101344

  7. Wafer-scale metasurface for total power absorption, local field enhancement and single molecule Raman spectroscopy

    Dongxing Wang; Wenqi Zhu; Michael D Best; Camden, Jon P.; Kenneth B. Crozier

    2013-01-01

    The ability to detect molecules at low concentrations is highly desired for applications that range from basic science to healthcare. Considerable interest also exists for ultrathin materials with high optical absorption, e.g. for microbolometers and thermal emitters. Metal nanostructures present opportunities to achieve both purposes. Metal nanoparticles can generate gigantic field enhancements, sufficient for the Raman spectroscopy of single molecules. Thin layers containing metal nanostruc...

  8. Self-absorption influence on the optical spectroscopy of zinc oxide laser produced plasma

    De Posada, E; Arronte, M A; Ponce, L; Rodriguez, E; Flores, T [Centro de Investigacion en Ciencia Aplicada y TecnologIa Avanzada-Unidad Altamira, Tamaulipas (Mexico); Lunney, J G, E-mail: edeposada@ipn.mx [School of Physics, Trinity College Dublin (Ireland)

    2011-01-01

    Optical spectroscopy is used to study the laser ablation process of ZnO targets. It is demonstrated that even if Partial Local Thermal Equilibrium is present, self absorption process leads to a decrease of recorded lines emission intensities and have to be taken into account to obtain correct values of such parameters. It is presented a method that combines results of both Langmuir probe technique and Anisimov model to obtain correct values of plasma parameters.

  9. Self-absorption influence on the optical spectroscopy of zinc oxide laser produced plasma

    Optical spectroscopy is used to study the laser ablation process of ZnO targets. It is demonstrated that even if Partial Local Thermal Equilibrium is present, self absorption process leads to a decrease of recorded lines emission intensities and have to be taken into account to obtain correct values of such parameters. It is presented a method that combines results of both Langmuir probe technique and Anisimov model to obtain correct values of plasma parameters.

  10. Theory of Attosecond Transient Absorption Spectroscopy of Krypton for Overlapping Pump and Probe Pulses

    Pabst, Stefan; Sytcheva, Arina; Moulet, Antoine; Wirth, Adrian; Goulielmakis, Eleftherios; Santra, Robin

    2012-01-01

    We present the first fully ab initio calculations for attosecond transient absorption spectroscopy of atomic krypton with overlapping pump and probe pulses. Within the time-dependent configuration interaction singles (TDCIS) approach, we describe the pump step (strong-field ionization using a near-infrared pulse) as well as the probe step (resonant electron excitation using an extreme- ultraviolet pulse) from first principles. We extent our TDCIS model and account for the spin-orbit splitting...

  11. Ultrafast Strong-Field Vibrational Dynamics Studied by Femtosecond Extreme-Ultraviolet Transient Absorption Spectroscopy

    Hosler, Erik Robert

    2013-01-01

    Femtosecond time-resolved extreme-ultraviolet core-level absorption spectroscopy has developed into a powerful tool for investigating chemical dynamics due to its sensitivity for detecting changes in electronic structure. By probing the core-levels of atoms and molecules, dynamics may be monitored with elemental specificity, as well as localized sensitivity to the oxidation state around the atomic absorber. Previous experiments with this technique demonstrated the capability to quantitatively...

  12. Application of FTIR Absorption Spectroscopy to Characterize Waste and Biofuels for Pyrolysis and Gasification

    KALISZ Sylwester; Svoboda, Karel; ROBAK Zbigniew; Baxter, David; Andersen, Lars

    2008-01-01

    The paper discusses the various applications of FTIR absorption spectroscopy as a tool for characterizing waste biofuels for pyrolysis and gasification. The FTIR spectrometer used in the study allows for analysis of solid and liquid waste and biofuel samples. Further, an attached dedicated gas cell is used in the characterization of gases evolving during pyrolysis in a versatile pyrolyser/gasifier attached to the FTIR. The pyrolyser operates in a batch mode and generates large quantities o...

  13. X-ray absorption spectroscopy beyond the core-hole lifetime

    A new technique to overcome the core-hole lifetime broadening in x-ray absorption spectroscopy is presented. It utilizes a high resolution fluorescence spectrometer which can be used to analyze the fluorescence photon energy with better resolution than the natural lifetime width. Furthermore, the high resolution spectrometer can also be used to select the final state in the fluorescence process which can offer spin selectivity even without long range magnetic order in the sample

  14. Energy-dispersive X-ray absorption spectroscopy at LNLS: investigation on strongly correlated metal oxides

    Cezar, Julio C.; Souza-Neto, Narcizo,; Piamonteze, Cınthia; Tamura, Edilson; Garcia, Flavio; Carvalho, Edson J.; Neueschwander, Régis T.; Ramos, Aline Y.; Tolentino, Hélio; Caneiro, Alberto; Massa, Nestor E.; Jesus Martinez-Lope, Maria; Antonio Alonso, Jose; Itié, Jean-Paul

    2010-01-01

    An energy-dispersive X-ray absorption spectroscopy beamline mainly dedicated to X-ray magnetic circular dichroism (XMCD) and material science under extreme conditions has been implemented in a bending-magnet port at the Brazilian Synchrotron Light Laboratory. Here the beamline technical characteristics are described, including the most important aspects of the mechanics, optical elements and detection set-up. The beamline performance is then illustrated through two case studies on strongly co...

  15. Quantum cascade laser absorption spectroscopy as a plasma diagnostic tool: an overview

    Jürgen Röpcke; Norbert Lang; Marko Hübner; Frank Hempel; Stefan Welzel; Davies, Paul B.

    2010-01-01

    The recent availability of thermoelectrically cooled pulsed and continuous wave quantum and inter-band cascade lasers in the mid-infrared spectral region has led to significant improvements and new developments in chemical sensing techniques using in-situ laser absorption spectroscopy for plasma diagnostic purposes. The aim of this article is therefore two-fold: (i) to summarize the challenges which arise in the application of quantum cascade lasers in such environments, and, (ii) to provide ...

  16. Simultaneous detection of potassium, water vapor and temperature with tunable diode laser absorption spectroscopy

    Norén, Edvin

    2015-01-01

    Existing tunable diode laser absorption spectroscopy (TDLAS) sensors for potassium (K) and for water vapor (H2O) and temperature were combined to enable simultaneous measurements in combustion and gasification processes. In-situ real-time detection of the above mentioned combustion parameters will improve the understanding of ash-formation during thermochemical conversion of biomass. Simultaneous measurements facilitate the experimental procedure and decrease the methodological uncertainty in...

  17. Third order nonlinear optical susceptibility of fluorescein-containing polymers determined by electro-absorption spectroscopy

    Gomez-Sosa, Gustavo; Beristain, Miriam F.; Ortega, Alejandra; Martínez-Viramontes, Jaquelin; Ogawa, Takeshi; Fernández-Hernández, Roberto C.; Tamayo-Rivera, Lis; Reyes-Esqueda, Jorge-Alejandro; Isoshima, Takashi; Hara, Masahiko

    2012-03-01

    Novel polymers containing xanthene groups with high dye concentrations were prepared, and their third order nonlinear optical properties were studied by electroabsorption spectroscopy technique. The polymers were amorphous with refractive indices above 1.6 in the non-resonant region. The UV-Visible absorption spectra indicate the fluoresceins molecules in the polymers are H-aggregated. They showed third order nonlinear susceptibility, χ(3) (-ω:ω, 0, 0), of 2.5-3.5 × 10-12 esu.

  18. Determination of vanadium in food and traditional Chinese medicine by graphite furnace atomic absorption spectroscopy

    2003-01-01

    Various experimental conditions were described for the vanadium determination by graphite furnace atomic ab-sorption spectroscopy (GFAAS). The experiments showed that when atomization took place under the conditions where thecombination of a pyrolytic coating graphite tube and fast raising temperature were used and the temperature was stable, thesignal peak shapes could be improved, the sensitivity was enhanced, and the memory effect was removed. The vanadium infood and traditional Chinese medicinal herbs can be accurately determined using the standard curve method.

  19. Elemental analysis of hair samples using energy dispersive X-ray fluorescence and atomic absorption spectroscopy

    Elemental analysis of hair samples was performed using energy dispersive X-ray fluorescence. The ion exchange preconcentration technique was employed. The capacity of the exchanger used-cellulose hyphan at different pH was investigated to determine the optimum pH for the resin. The capacity of the resin to take up elements of interest from mixed solutions was also analysed using atomic absorption spectroscopy. (author)

  20. Differential Optical-absorption Spectroscopy (doas) System For Urban Atmospheric-pollution Monitoring

    Edner, H; Ragnarson, P; Spannare, S; Svanberg, Sune

    1993-01-01

    We describe a fully computer-controlled differential optical absorption spectroscopy system for atmospheric air pollution monitoring. A receiving optical telescope can sequentially tune in to light beams from a number of distant high-pressure Xe lamp light sources to cover the area of a medium-sized city. A beam-finding servosystem and automatic gain control permit unattended long-time monitoring. Using an astronomical code, we can also search and track celestial sources. Selected wavelength ...

  1. Characterization of metalloproteins by high-throughput X-ray absorption spectroscopy

    Shi, W.; Punta, M.; J. Bohon; J.M. Sauder; R D'Mello; Sullivan, M.; Toomey, J.; Abel, D; Lippi, M.; Passerini, A.; P. Frasconi; Burley, S K; B. Rost; Chance, M. R.

    2011-01-01

    High-throughput X-ray absorption spectroscopy was used to measure transition metal content based on quantitative detection of X-ray fluorescence signals for 3879 purified proteins from several hundred different protein families gen- erated by the New York SGX Research Center for Structural Genomics. Approximately 9% of the proteins analyzed showed the presence of transition metal atoms (Zn, Cu, Ni, Co, Fe, or Mn) in stoichiometric amounts. The method is highly automated and highly reliable ba...

  2. Time-resolved tunable diode laser absorption spectroscopy of pulsed plasma

    Adámek, Petr; Olejníček, Jiří; Čada, Martin; Kment, Š.; Hubička, Zdeněk

    2013-01-01

    Roč. 38, č. 14 (2013), s. 2428-2430. ISSN 0146-9592 R&D Projects: GA MŠk LH12045; GA ČR(CZ) GAP205/11/0386; GA MŠk LD12002; GA MŠk LH12043 Institutional support: RVO:68378271 Keywords : diode lasers * plasma diagnostics * absorption spectroscopy * time resolved Subject RIV: BL - Plasma and Gas Discharge Physics Impact factor: 3.179, year: 2013

  3. In situ x-ray-absorption spectroscopy study of hydrogen absorption by nickel-magnesium thin films

    Structural and electronic properties of co-sputtered Ni-Mg thin films with varying Ni to Mg ratio were studied by in situ x-ray absorption spectroscopy in the Ni L-edge and Mg K-edge regions. Codeposition of the metals led to increased disorder and decreased coordination around Ni and Mg compared to pure metal films. Exposure of the metallic films to hydrogen resulted in formation of hydrides and increased disorder. The presence of hydrogen as a near neighbor around Mg caused a drastic reduction in the intensities of multiple scattering resonances at higher energies. The optical switching behavior and changes in the x-ray spectra varied with Ni to Mg atomic ratio. Pure Mg films with Pd overlayers were converted to MgH2: The H atoms occupy regular sites as in bulk MgH2. Although optical switching was slow in the absence of Ni, the amount of H2 absorption was large. Incorporation of Ni in Mg films led to an increase in the speed of optical switching but decreased maximum transparency. Significant shifts in the Ni L3 and L2 peaks are consistent with strong interaction with hydrogen in the mixed films

  4. Spectroscopy of PTCDA attached to rare gas samples: clusters vs. bulk matrices. I. Absorption spectroscopy

    Dvorak, M.; Müller, M; Knoblauch, T.; Bünermann, O.; Rydlo, A.; Minniberger, S.; Harbich, W.; Stienkemeier, F.

    2012-01-01

    The interaction between PTCDA (3,4,9,10-perylene-tetracarboxylic-dianhydride) and rare gas or para-hydrogen samples is studied by means of laser-induced fluorescence excitation spectroscopy. The comparison between spectra of PTCDA embedded in a neon matrix and spectra attached to large neon clusters shows that these large organic molecules reside on the surface of the clusters when doped by the pick-up technique. PTCDA molecules can adopt different conformations when attached to argon, neon a...

  5. An approach of open-path gas sensor based on tunable diode laser absorption spectroscopy

    Hui Xia; Wenqing Liu; Yujun Zhang; Ruifeng Kan; Min Wang; Ying He; Yiben Cui; Jun Ruan; Hui Geng

    2008-01-01

    Tunable diode laser absorption spectroscopy (TDLAS) is a new method to detect trace-gas qualitatively or quantificationally based on the scan characteristic of the diode laser to obtain the absorption spectroscopy in the characteristic absorption region. A time-sharing scanning open-path TDLAS system using two near infrared distributed feedback (DFB) tunable diode lasers is designed to detect CH4 and H2S in leakage of natural gas. A low-cost Fresnel lens is used in this system as receiving optics which receives the laser beam reflected by a solid corner cube reflector with a distance of up to about 60 m. High sensitivity is achieved by means of wavelength-modulation spectroscopy with second-harmonic detection. The minimum detection limits of 1.1 ppm·m for CH4 and 15 ppm·m for H2S are demonstrated with a total optical path of 120 m. The simulation monitoring experiment of nature gas leakage was carried out with this system. According to the receiving light efficiency of optical system and detectable minimum light intensity of detection, the detectable optical path of the system can achieve 1 - 2 km. The sensor is suitable for natural gas leakage monitoring application.

  6. Structural study of tungstate fluorophosphate glasses by Raman and X-ray absorption spectroscopy

    Transparent glasses were synthesized in the NaPO3-BaF2-WO3 ternary system and several structural characterizations were performed by X-ray absorption spectroscopy (XANES) at the tungsten LI and LIII absorption edges and by Raman spectroscopy. Special attention was paid to the coordination state of tungsten atoms in the vitreous network. XANES investigations showed that tungsten atoms are only six-fold coordinated (octahedra WO6) and that these glasses are free of tungstate tetrahedra (WO4). In addition, Raman spectroscopy allowed to identify a break in the linear phosphate chains as the amount of WO3 increases and the formation of P-O-W bonds in the vitreous network indicating the modifier behavior of WO6 octahedra in the glass network. Based on XANES data, we suggested a new attribution of several Raman absorption bands which allowed to identify the presence of W-O- and W=O terminal bonds and a progressive apparition of W-O-W bridging bonds for the most WO3 concentrated samples (30% molar) due to the formation of WO6 clusters

  7. Sulfur K-edge X-ray absorption spectroscopy of petroleum asphaltenes and model compounds

    The utility of sulfur K-edge X-ray absorption spectroscopy for the determination and quantification of sulfur forms in petroleum asphaltenes has been investigated. Both X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) spectra were obtained for a selected group of model compounds and for several petroleum asphaltene samples. For the model compounds the sulfur XANES was found to vary widely from compound to compound and to provide a fingerprint for the form of sulfur involved. The use of third derivatives of the spectra enabled discrimination of mixtures of sulfidic and thiophenic model compounds and allowed approximate quantification of the amount of each component in the mixtures and in the asphaltene samples. These results represent the first demonstration that nonvolatile sulfur forms can be distinguished and approximately quantified by direct measurement

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

    Lamberti, Carlo

    2016-01-01

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

  9. Wafer-scale metasurface for total power absorption, local field enhancement and single molecule Raman spectroscopy

    Wang, Dongxing; Zhu, Wenqi; Best, Michael D.; Camden, Jon P.; Crozier, Kenneth B.

    2013-01-01

    The ability to detect molecules at low concentrations is highly desired for applications that range from basic science to healthcare. Considerable interest also exists for ultrathin materials with high optical absorption, e.g. for microbolometers and thermal emitters. Metal nanostructures present opportunities to achieve both purposes. Metal nanoparticles can generate gigantic field enhancements, sufficient for the Raman spectroscopy of single molecules. Thin layers containing metal nanostructures (“metasurfaces”) can achieve near-total power absorption at visible and near-infrared wavelengths. Thus far, however, both aims (i.e. single molecule Raman and total power absorption) have only been achieved using metal nanostructures produced by techniques (high resolution lithography or colloidal synthesis) that are complex and/or difficult to implement over large areas. Here, we demonstrate a metasurface that achieves the near-perfect absorption of visible-wavelength light and enables the Raman spectroscopy of single molecules. Our metasurface is fabricated using thin film depositions, and is of unprecedented (wafer-scale) extent. PMID:24091825

  10. Aspects of UV-absorption spectroscopy on ozone in effluents of plasma jets operated in air

    Cold plasmas operating under atmospheric conditions have been in the focus of scientific attention not only due to their use in plasma medicine. Many of these plasma sources most notably produce ozone. This work presents a detailed ozone analysis on an atmospheric-pressure plasma jet operated in ambient air using ultraviolet (UV) absorption spectroscopy. A special focus is placed on the question whether other species are involved, or is the absorption signal due to ozone. For this, the wavelength dependence of the optical depth was measured and compared with the theoretical optical depth including the cross section of ozone. The results show that in the case of a MHz frequency driven atmospheric-pressure argon plasma jet the absorption signal in the UV range is solely due to ozone. Furthermore, this finding is verified by spectroscopic measurements in the IR spectral range. Additional space-resolved ozone density measurements are performed in the effluent of this jet with small oxygen admixtures by means of UV absorption spectroscopy. A funnel-shaped spatial ozone profile is found for all investigated oxygen admixtures. The highest ozone density develops on the effluent axis and in close vicinity to the jet nozzle. The maximal detected value is 1.5 × 1016 cm-3 for an oxygen admixture of 1%. In order to compare the results with non-space-resolved ozone detection methods the ozone net production rate is calculated.

  11. An energy dispersive x-ray absorption spectroscopy beamline, X6A, at NSLS

    An energy dispersive x-ray absorption spectroscopy instrument has been built at the X6A beam port of the x-ray ring at the National Synchrotron Light Source (NSLS). This instrument allows the collection of extended x-ray-absorption fine structure and/or x-ray absorption near-edge structure spectra for many elements on the millisecond time scale. The beamline employs a four-point crystal bender and a rectangular Si 220 crystal to access incident energies between 6.5 and 21 keV. Because the polychromator focuses the synchrotron beam to a narrow 100-μm line, this experimental apparatus is ideal for x-ray absorption spectroscopy experiments in special environments such as at high pressures, for in situ experiments, and/or for very small samples. In this manuscript we will describe the instrument design and present data with which to evaluate the instrument. This beamline is available through the NSLS user proposal system

  12. Broadband Cavity Enhanced Differential Optical Absorption Spectroscopy (CE-DOAS – applicability and corrections

    D. Pöhler

    2009-11-01

    Full Text Available Atmospheric trace gas measurements by cavity assisted long-path absorption spectroscopy are an emerging technology. An interesting approach is the combination of CEAS with broadband light sources, the broadband CEAS (BB-CEAS. BB-CEAS lends itself to the application of the DOAS technique to analyse the derived absorption spectra. While the DOAS approach has enormous advantages in terms of sensitivity and specificity of the measurement, an important implication is the reduction of the light path by the trace gas absorption, since cavity losses due to absorption by gases reduce the quality (Q of the cavity. In fact, at wavelength, where the quality of the BB-CEAS cavity is dominated by the trace gas absorption (especially at very high mirror reflectivity, the average light path will vary nearly inversely with the trace gas concentration and the strength of the band will become only weakly dependent on the trace gas concentration c in the cavity, (the differential optical density being proportional to the logarithm of the trace gas concentration. Only in the limiting case where the mirror reflectivity determines Q at all wavelength, the strength of the band as seen by the CE-DOAS instrument becomes directly proportional to the concentration c. We investigate these relationships in detail and present methods to correct for the cases between the two above extremes, which are of course the important ones in practice.

  13. Broadband Cavity Enhanced Differential Optical Absorption Spectroscopy (CE-DOAS – applicability and corrections

    D. Pöhler

    2008-12-01

    Full Text Available Atmospheric trace gas measurements by cavity assisted long-path absorption spectroscopy are an emerging technology. An interesting approach is the combination of CEAS with broad band light sources, the broad-band CEAS (BB-CEAS. BB-CEAS lends itself to the application of the DOAS technique to analyse the derived absorption spectra. While the DOAS approach has enormous advantages in terms of sensitivity and specificity of the measurement, an important implication is the reduction of the light path by the trace gas absorption, since cavity losses due to absorption by gases reduce the quality (Q of the cavity. In fact, at wavelength, where the quality of the BB-CEAS cavity is dominated by the trace gas absorption (esp. at very high mirror reflectivity, the light path will vary inversely with the trace gas concentration and the strength of the band will become nearly independent of the trace gas concentration c in the cavity, rendering the CEAS Method useless for trace gas measurements. Only in the limiting case where the mirror reflectivity determines Q at all wavelength, the strength of the band as seen by the BB-CEAS instrument becomes proportional to the concentration c. We investigate these relationships in detail and present methods to correct for the cases between the two above extremes, which are of course the important ones in practice.

  14. [Study on removing the lamp spectrum structure in differential optical absorption spectroscopy].

    Qu, Xiao-ying; Li, Yu-jin

    2010-11-01

    Differential optical absorption spectroscopy (DOAS) technique has been used to measure trace gases in the atmosphere by their strongly structured absorption of radiation in the UV and visible spectral range, and nowadays this technique has been widely utilized to measure trace polluted gases in the atmosphere e.g. SO2, NO2, O3, HCHO, etc. However, there exists lamp (xenon lamp or deuteriumlamp) spectrum structure in the measured band (300-700 nm) of the absorption spectra of atmosphere, which badly impacts on precision of retrieving the concentration of trace gases in the atmosphere. People home and abroad generally employ two ways to handle this problem, one is segmenting band retrieving method, another is remedial retrieving method. In the present paper, a new retrieving method to deal with this trouble is introduced. The authors used moving-window average smoothing method to obtain the slow part of the absorption spectra of atmosphere, then achieved the lamp (xenon lamp in the paper) spectrum structure in the measured band of the absorption spectra of atmosphere. The authors analyzed and retrieved the measured spectrum of the atmosphere, and the result is better than the forenamed ways. Chi-square of residuum is 2.995 x 10(-4), and this method was proved to be able to avoid shortcoming of choosing narrowband and disadvantage of discovering the new component of atmosphere in retrieving the concentration of air pollutants and measuring the air pollutants. PMID:21284148

  15. The use of atomic absorption spectroscopy to measure arsenic, selenium, molybdenum, and vanadium in water and soil samples from uranium mill tailings sites

    Hollenbach, M.H.

    1988-01-01

    The Technical Measurements Center (TMC) was established to support the environmental measurement needs of the various DOE remedial action programs. A laboratory intercomparison study conducted by the TMC, using soil and water samples from sites contaminated by uranium mill tailings, indicated large discrepancies in analytical results reported by participating laboratories for arsenic, selenium, molybdenum, and vanadium. The present study was undertaken to investigate the most commonly used analytical techniques for measuring these four elements, ascertain routine and reliable quantification, and assess problems and successes of analysts. Based on a survey of the technical literature, the analytical technique of atomic absorption spectroscopy was selected for detailed study. The application of flame atomic absorption, graphite furnace atomic absorption, and hydride generation atomic absorption to the analysis of tailings-contaminated samples is discussed. Additionally, laboratory sample preparation methods for atomic absorption spectroscopy are presented. The conclusion of this report is that atomic absorption can be used effectively for the determination of arsenic, selenium, molybdenum, and vanadium in water and soil samples if the analyst understands the measurement process and is aware of potential problems. The problem of accurate quantification of arsenic, selenium, molybdenum, and vanadium in water and soil contaminated by waste products from uranium milling operations affects all DOE remedial action programs (Surplus Facilities Management Program (SFMP), Formerly Utilized Site Remedial Action Program (FUSRAP), and Uranium Mill Tailings Remedial Action Program (UMTRAP)), since all include sites where uranium was processed. 96 refs., 9 figs.

  16. Spectroscopy of PTCDA attached to rare gas samples: clusters vs. bulk matrices. I. Absorption spectroscopy

    Dvorak, M; Knoblauch, T; Bünermann, O; Rydlo, A; Minniberger, S; Harbich, W; Stienkemeier, F

    2012-01-01

    The interaction between PTCDA (3,4,9,10-perylene-tetracarboxylic-dianhydride) and rare gas or para-hydrogen samples is studied by means of laser-induced fluorescence excitation spectroscopy. The comparison between spectra of PTCDA embedded in a neon matrix and spectra attached to large neon clusters shows that these large organic molecules reside on the surface of the clusters when doped by the pick-up technique. PTCDA molecules can adopt different conformations when attached to argon, neon and para-hydrogen clusters which implies that the surface of such clusters has a well-defined structure and has not liquid or fluxional properties. Moreover, a precise analysis of the doping process of these clusters reveals that the mobility of large molecules on the cluster surface is quenched, preventing agglomeration and complex formation.

  17. Cavity Enhanced Absorption Spectroscopy with a red LED source for NOx trace analysis

    Ventrillard Courtillot, I.; Sciamma O'Brien, E.; Méjean, G.; Romanini, D.

    2009-04-01

    This study presents a high sensitivity absorption system using a red LED source emitting at 625 nm and a small CCD spectrometer as detector [1]. This system is based on IBB-CEAS (Incoherent Broad Band Cavity Enhanced Absorption Spectroscopy). The expected application is the measurement of NO2 and NO3 in urban concentration (ppbv and ppmv levels). The IBB-CEAS was firstly developed with arc lamps and then with LED. Systems based on this technique are easy to use, highly sensitive, compact and robust. They also are inexpensive. Existent techniques to measure NO2 and NO3 are generally slow or not sensitive enough and need frequently calibrations (chemical luminescent) or are characterized by a low spatial resolution (Long Path Differential Optical Absorption Spectroscopy). Previous works based on diodes lasers emitting around 410 nm and coupled with High Finess Cavity proved a highest sensibility than ppbv and a time measurement of 0.1 s [2]. This sensibility is necessary for measurements in unpolluted environment but a more expensive and more complex system is needed. NO2 is chosen for testing as it is stable and available in calibrated diluted samples. An excellent agreement in the range from 610 nm to 630 nm was gotten between an absorption spectrum obtained by IBB-CEAS and a spectrum calculated using a reference NO2 absorption cross section by Voigt et al [3] (after convolution with a 2.05-nm FWHM Gaussian simulating our spectrometer response function). The reflectivity of the mirrors was determined with a commercial spectrophotometer and was used to deduce the absorption spectrum of NO2 from the transmission spectrum of the cavity. We obtained by estimating the sensitivity of our setup from the noise in a baseline measurement of absorption, (standard deviation = 2E-10 cm-1). This corresponds (under atmospheric conditions) to a sensitivity about 0.5 ppbv. NO3 cross-section absorption is 600 times higher than the NO2 (at 623 nm), so a detection limit of 1 pptv is

  18. X-ray-induced photo-chemistry and X-ray absorption spectroscopy of biological samples

    George, Graham N.; Pickering, Ingrid J.; Pushie, M. Jake; Nienaber, Kurt; Hackett, Mark J.; Ascone, Isabella; Hedman, Britt; Hodgson, Keith O.; Aitken, Jade B.; Levina, Aviva; Glover, Christopher; Lay, Peter A.

    2012-01-01

    X-ray-induced photo-chemistry of metal sites within biological molecules is a concern for X-ray absorption spectroscopy, X-ray crystallography and other techniques in which samples are illuminated with X-rays. The effects of X-ray-induced photo-chemistry are reviewed and the methods used to mitigate these in X-ray absorption spectroscopy are outlined.

  19. Femtosecond x-ray absorption spectroscopy with hard x-ray free electron laser

    Katayama, Tetsuo; Togashi, Tadashi; Tono, Kensuke; Kameshima, Takashi [Japan Synchrotron Radiation Research Institute, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan); Inubushi, Yuichi; Sato, Takahiro; Hatsui, Takaki; Yabashi, Makina [RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5148 (Japan); Obara, Yuki; Misawa, Kazuhiko [Department of Applied Physics, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588 (Japan); Bhattacharya, Atanu; Kurahashi, Naoya [Department of Chemistry, Graduate School of Science, Kyoto University, Kitashirakawa-Oiwakecho, Sakyo-ku, Kyoto 606-8502 (Japan); Ogi, Yoshihiro [Molecular Reaction Dynamics Research Team, RIKEN Center for Advanced Photonics, 2-1 Hirosawa, Wako 351-0198 (Japan); Suzuki, Toshinori [Department of Chemistry, Graduate School of Science, Kyoto University, Kitashirakawa-Oiwakecho, Sakyo-ku, Kyoto 606-8502 (Japan); Molecular Reaction Dynamics Research Team, RIKEN Center for Advanced Photonics, 2-1 Hirosawa, Wako 351-0198 (Japan)

    2013-09-23

    We have developed a method of dispersive x-ray absorption spectroscopy with a hard x-ray free electron laser (XFEL), generated by a self-amplified spontaneous emission (SASE) mechanism. A transmission grating was utilized for splitting SASE-XFEL light, which has a relatively large bandwidth (ΔE/E ∼ 5 × 10{sup −3}), into several branches. Two primary split beams were introduced into a dispersive spectrometer for measuring signal and reference spectra simultaneously. After normalization, we obtained a Zn K-edge absorption spectrum with a photon-energy range of 210 eV, which is in excellent agreement with that measured by a conventional wavelength-scanning method. From the analysis of the difference spectra, the noise ratio was evaluated to be ∼3 × 10{sup −3}, which is sufficiently small to trace minute changes in transient spectra induced by an ultrafast optical laser. This scheme enables us to perform single-shot, high-accuracy x-ray absorption spectroscopy with femtosecond time resolution.

  20. Femtosecond x-ray absorption spectroscopy with hard x-ray free electron laser

    We have developed a method of dispersive x-ray absorption spectroscopy with a hard x-ray free electron laser (XFEL), generated by a self-amplified spontaneous emission (SASE) mechanism. A transmission grating was utilized for splitting SASE-XFEL light, which has a relatively large bandwidth (ΔE/E ∼ 5 × 10−3), into several branches. Two primary split beams were introduced into a dispersive spectrometer for measuring signal and reference spectra simultaneously. After normalization, we obtained a Zn K-edge absorption spectrum with a photon-energy range of 210 eV, which is in excellent agreement with that measured by a conventional wavelength-scanning method. From the analysis of the difference spectra, the noise ratio was evaluated to be ∼3 × 10−3, which is sufficiently small to trace minute changes in transient spectra induced by an ultrafast optical laser. This scheme enables us to perform single-shot, high-accuracy x-ray absorption spectroscopy with femtosecond time resolution

  1. Real time tracing of valence-shell electronic coherences with attosecond transient absorption spectroscopy

    Wirth, A. [Max-Planck-Institut für Quantenoptik, Hans-Kopfermann-Str. 1, D-85748 Garching (Germany); Santra, R. [Center for Free-Electron Laser Science, DESY, Notkestrasse 85, 22607 Hamburg (Germany); Department of Physics, University of Hamburg, Jungiusstrasse 9, 20355 Hamburg (Germany); Goulielmakis, E., E-mail: elgo@mpq.mpg.de [Max-Planck-Institut für Quantenoptik, Hans-Kopfermann-Str. 1, D-85748 Garching (Germany)

    2013-03-12

    Highlights: ► Detailing the technique of attosecond transient absorption spectroscopy. ► Tracing the charge state time-resolved ionization of atoms. ► Real-time observation and reconstruction of valence electron motion in Kr{sup +} ions. ► Observation of coherences in correlated multi-hole systems: Kr{sup 2+} and xenon ions. - Abstract: The chemical properties of atoms, molecules and of more complex systems such as clusters, nanoparticles or condensed matter systems are determined by valence electrons. Real-time control of these properties requires the capability of tracing as well as of driving valence electrons on their native temporal scale of motion, that is, within tens to thousands of attoseconds. Here we detail the technique of attosecond transient absorption spectroscopy. It combines the extreme sensitivity of core-level spectroscopy with the unprecedented temporal resolution offered by the tools of attosecond technology. We use the technique to demonstrate real-time tracing and complete characterization of coherent electron motion triggered by single, double or multiple ionization of atoms exposed to intense, few-cycle pulses. Our work opens the door to high fidelity, time-domain studies and control of electron dynamics in the microcosm.

  2. Infrared reflection absorption spectroscopy study of radiation-heterogeneous processes in the system of aluminum-hexane

    Full text: Infrared reflection absorption spectroscopy (IRRAS) was applied to study the regularities of radiation conversion of hexane on the surface of aluminum. The research object was the thin polished aluminum plate by mark of AD-00 with reflection coefficient R=0.8†0.85 in infrared range λ=2.2†15 μ . As adsorbate unsaturated vapors of spectroscopy clear hexane were used. The absorption of hexane (C2H14) was being studied manometric at pressures P=(0.1†1.0)·102 Pa , what corresponded to monolayer value of 1-10. The samples were irradiated with γ-quanta of 60Co with D=1.03 Gy·s-1 doze rate. Infrared reflection spectrum when linear-polarized radiation fall on the sample under angle ψ=10o was measured by spectrophotometer 'Specord 71 JR' in diapason of 4000-650cm-1 at the temperature by mean of special reflecting arrangements. Formation of molecular hydrogen (H2) and other gaseous products of decomposition were controlled by chromotographical and infrared spectroscopical methods. The analysis of hexane infrared absorption spectra after radiation-stimulated adsorption on the surface of aluminum, points out the formation of H-bonded hydrocarbon complex ( ν∼2680cm-1) with much loosening of C-H bond (the molecular form of absorption) and the possibility of proceeding dissociative absorption with formation of metal-alkyls (ν∼2880, 2920, 2970 cm-1). Probability of the last mentioned process, which proceeds in the most defective centers, increases with increasing of γ-radiation doze. It was established that the radiation processes in hetero system Al-ads.C6H14 accelerate the radiolysis of hexane. At all these the radiation decomposition of hexane in hetero system Al-ads.C6H14 is accompanied by formation the surface hydrides (ν∼1700-2000 cm-1), acetylene (ν∼3200-3300 cm-1), ethylene (ν∼980 cm-1), and also gaseous products of molecular hydrogen decomposition (H2) and hydrocarbons C1-C5 (bands with maxima 770, 790, 825, 900 and 950 cm-1 concern

  3. Ultra-fast X-ray absorption spectroscopy for the study of matter in transient regime

    In this work, we study the physics of dense matter, plasmas or solids, using X-ray absorption spectroscopy. Through the use of sources produced by laser-matter interaction, we have measured the absorption spectra of aluminum and bromine plasmas, as well as those of vanadium dioxide (VO2). The measurement of absorption coefficients allows us to probe the dense matter and to study its properties. The experiments are carried out following the same principle: they use the same experimental set-up, called pump-probe. When the matter is dense, the absorption properties of an atom are modified by the surrounding environment. In a plasma, it is mainly the bound- bound transitions which are altered: the shapes of those spectral rays are modified. In a solid, the position of the neighbouring atoms in relation to the absorbing atom modify the structure of absorption levels (bound-free transition). The study of this structure allows us to measure the parameters of the material, and provides information such as the state of the electronic band or the interatomic gaps. The experiments carried out at the LULI have allowed us to probe plasmas in the relatively unknown regime of the Warm Dense Matter. One of the key parameters is that the plasma is characterised independently (FDI diagnostic). It allows for a better comparison of the measured absorption against a calculation made with the numerical model OPA-S. The experiments carried out at INRS have led to the realisation of an experimental system having the characteristics which allow the study of the dynamics of solids showing ultra-fast phase transition. For those experiments, we have used vanadium dioxide as a model system allowing us to test the feasibility of the method. (author)

  4. Tunable Diode Laser Atomic Absorption Spectroscopy for Detection of Potassium under Optically Thick Conditions.

    Qu, Zhechao; Steinvall, Erik; Ghorbani, Ramin; Schmidt, Florian M

    2016-04-01

    Potassium (K) is an important element related to ash and fine-particle formation in biomass combustion processes. In situ measurements of gaseous atomic potassium, K(g), using robust optical absorption techniques can provide valuable insight into the K chemistry. However, for typical parts per billion K(g) concentrations in biomass flames and reactor gases, the product of atomic line strength and absorption path length can give rise to such high absorbance that the sample becomes opaque around the transition line center. We present a tunable diode laser atomic absorption spectroscopy (TDLAAS) methodology that enables accurate, calibration-free species quantification even under optically thick conditions, given that Beer-Lambert's law is valid. Analyte concentration and collisional line shape broadening are simultaneously determined by a least-squares fit of simulated to measured absorption profiles. Method validation measurements of K(g) concentrations in saturated potassium hydroxide vapor in the temperature range 950-1200 K showed excellent agreement with equilibrium calculations, and a dynamic range from 40 pptv cm to 40 ppmv cm. The applicability of the compact TDLAAS sensor is demonstrated by real-time detection of K(g) concentrations close to biomass pellets during atmospheric combustion in a laboratory reactor. PMID:26938713

  5. Measurement of temperature profiles in flames by emission-absorption spectroscopy

    Simmons, F. S.; Arnold, C. B.; Lindquist, G. H.

    1972-01-01

    An investigation was conducted to explore the use of infrared and ultraviolet emission-absorption spectroscopy for determination of temperature profiles in flames. Spectral radiances and absorptances were measured in the 2.7-micron H2O band and the 3064-A OH band in H2/O2 flames for several temperature profiles which were directly measured by a sodium line-reversal technique. The temperature profiles, determined by inversion of the infrared and ultraviolet spectra, showed an average disagreement with line-reversal measurements of 50 K for the infrared and 200 K for the ultraviolet at a temperature of 2600 K. The reasons for these discrepancies are discussed in some detail.

  6. [Measurement of OH radicals in flame with high resolution differential optical absorption spectroscopy].

    Liu, Yu; Liu, Wen-Qing; Kan, Rui-Feng; Si, Fu-Qi; Xu, Zhen-Yu; Hu, Ren-Zhi; Xie, Pin-Hua

    2011-10-01

    The present paper describes a new developed high resolution differential optical absorption spectroscopy instrument used for the measurement of OH radicals in flame. The instrument consists of a Xenon lamp for light source; a double pass high resolution echelle spectrometer with a resolution of 3.3 pm; a multiple-reflection cell of 20 meter base length, in which the light reflects in the cell for 176 times, so the whole path length of light can achieve 3 520 meters. The OH radicals'6 absorption lines around 308 nm were simultaneously observed in the experiment. By using high resolution DOAS technology, the OH radicals in candles, kerosene lamp, and alcohol burner flames were monitored, and their concentrations were also inverted. PMID:22250529

  7. Simulating systematic errors in X-ray absorption spectroscopy experiments: Sample and beam effects

    The article presents an analytical model to simulate experimental imperfections in the realization of an X-ray absorption spectroscopy experiment, performed in transmission or fluorescence mode. Distinction is made between sources of systematic errors on a time-scale basis, to select the more appropriate model for their handling. For short time-scale, statistical models are the most suited. For large time-scale, the model is developed for sample and beam imperfections: mainly sample inhomogeneity, sample self-absorption, beam achromaticity. The ability of this model to reproduce the effects of these imperfections is exemplified, and the model is validated on real samples. Various potential application fields of the model are then presented

  8. Constraining Variable High Velocity Winds from Broad Absorption Line Quasars with Multi-Epoch Spectroscopy

    Haggard, Daryl; Green, Paul J; Aldcroft, Tom; Anderson, Scott F

    2012-01-01

    Broad absorption line (BAL) quasars probe the high velocity gas ejected by luminous accreting black holes. BAL variability timescales place constraints on the size, location, and dynamics of the emitting and absorbing gas near the supermassive black hole. We present multi-epoch spectroscopy of seventeen BAL QSOs from the Sloan Digital Sky Survey (SDSS) using the Fred Lawrence Whipple Observatory's 1.5m telescope's FAST Spectrograph. These objects were identified as BALs in SDSS, observed with Chandra, and then monitored with FAST at observed-frame cadences of 1, 3, 9, 27, and 81 days, as well as 1 and 2 years. We also monitor a set of non-BAL quasars with matched redshift and luminosity as controls. We identify significant variability in the BALs, particularly at the 1 and 2 year cadences, and use its magnitude and frequency to constrain the outflows impacting the broad absorption line region.

  9. Sensitive CH4 detection applying quantum cascade laser based optical feedback cavity-enhanced absorption spectroscopy.

    Lang, N; Macherius, U; Wiese, M; Zimmermann, H; Röpcke, J; van Helden, J H

    2016-03-21

    We report on sensitive detection of atmospheric methane employing quantum cascade laser based optical feedback cavity-enhanced absorption spectroscopy (OF-CEAS). An instrument has been built utilizing a continuous-wave distributed feedback quantum cascade laser (cw-QCL) with a V-shaped cavity, a common arrangement that reduces feedback to the laser from non-resonant reflections. The spectrometer has a noise equivalent absorption coefficient of 3.6 × 10-9 cm-1 Hz-1/2 for a spectral scan of CH4 at 7.39 μm. From an Allan-Werle analysis a detection limit of 39 parts per trillion of CH4 at atmospheric pressure within 50 s acquisition time was found. PMID:27136874

  10. Reflection-Absorption Infrared Spectroscopy of Thin Films Using an External Cavity Quantum Cascade Laser

    Phillips, Mark C.; Craig, Ian M.; Blake, Thomas A.

    2013-02-04

    We present experimental demonstrations using a broadly tunable external cavity quantum cascade laser (ECQCL) to perform Reflection-Absorption InfraRed Spectroscopy (RAIRS) of thin layers and residues on surfaces. The ECQCL compliance voltage was used to measure fluctuations in the ECQCL output power and improve the performance of the RAIRS measurements. Absorption spectra from self-assembled monolayers of a fluorinated alkane thiol and a thiol carboxylic acid were measured and compared with FTIR measurements. RAIRS spectra of the explosive compounds PETN, RDX, and tetryl deposited on gold substrates were also measured. Rapid measurement times and low noise were demonstrated, with < 1E-3 absorbance noise for a 10 second measurement time.

  11. The nature of arsenic in uranium mill tailings by X-ray absorption spectroscopy

    In order to understand the evolving world of environmental issues, the ability to characterize and predict the stability and bioavailability of heavy metal contaminants in mine waste is becoming increasingly more important. X-ray Absorption Near Edge Structure (XANES) and Extended X-ray Absorption Fine Structure (EXAFS) spectroscopies were used to characterize a series of synthetic and natural samples associated with mine tailings processing. XANES was shown to be excellent as a tool to rapidly differentiate oxidation states of arsenic within the samples. The EXAFS spectra provided information on the mineralogy of the precipitated raffinate and tailings and showed that these samples are composed of a mixture of amorphous ferric arsenates, adsorbed arsenates and a mixture of other poorly ordered arsenates. (authors)

  12. Picosecond time-resolved X-ray absorption spectroscopy of ultrafast aluminum plasmas.

    Audebert, P; Renaudin, P; Bastiani-Ceccotti, S; Geindre, J-P; Chenais-Popovics, C; Tzortzakis, S; Nagels-Silvert, V; Shepherd, R; Matsushima, I; Gary, S; Girard, F; Peyrusse, O; Gauthier, J-C

    2005-01-21

    We have used point-projection K-shell absorption spectroscopy to infer the ionization and recombination dynamics of transient aluminum plasmas. Two femtosecond beams of the 100 TW laser at the LULI facility were used to produce an aluminum plasma on a thin aluminum foil (83 or 50 nm), and a picosecond x-ray backlighter source. The short-pulse backlighter probed the aluminum plasma at different times by adjusting the delay between the two femtosecond driving beams. Absorption x-ray spectra at early times are characteristic of a dense and rather homogeneous plasma. Collisional-radiative atomic physics coupled with hydrodynamic simulations reproduce fairly well the measured average ionization as a function of time. PMID:15698184

  13. Ground-based imaging differential optical absorption spectroscopy of atmospheric gases.

    Lohberger, Falko; Hönninger, Gerd; Platt, Ulrich

    2004-08-20

    We describe a compact remote-sensing instrument that permits spatially resolved mapping of atmospheric trace gases by passive differential optical absorption spectroscopy (DOAS) and present our first applications of imaging of the nitrogen dioxide contents of the exhaust plumes of two industrial emitters. DOAS permits the identification and quantification of various gases, e.g., NO2, SO2, and CH2O, from their specific narrowband (differential) absorption structures with high selectivity and sensitivity. With scattered sunlight as the light source, DOAS is used with an imaging spectrometer that is simultaneously acquiring spectral information on the incident light in one spatial dimension (column). The second spatial dimension is scanned by a moving mirror. PMID:15352396

  14. [Measurement and retrieval of indicators for fast VOCs atmospheric photochemistry with differential optical absorption spectroscopy].

    Peng, Fu-Min; Xie, Pin-Hua; Shao, Shi-Yong; Li, Yu-Jin; Lin, Yi-Hui; Li, Su-Wen; Qin, Min; Liu, Wen-Qing

    2008-03-01

    Featuring excellent response characteristics and detection sensitivity and with much lower operational cost, differential optical absorption spectroscopy (DOAS) can be a powerful tool to trace concentration variation of trace indicators -O3, Ox (O3 + NO2) and HCHO for fast VOCs atmospheric photochemistry. But it's difficult to measure those gases accurately because of trace concentration. Here using a self-made DOAS system, the accurate measurement of those indicators was achieved through improving the ratio of signal to noise ratio and correcting the background scattering light; the retrieving method of those indicators was developed through eliminating the temperature effect of absorption cross section, accurately removing the intrinsic structure and lamp structure of spectrum. The preference of different spectral windows that could be used for the concentration retrieval of those indicators was analyzed and compared including interfering factors, results retrieved and the accuracy. PMID:18536400

  15. Strontium Localization in Bone Tissue Studied by X-Ray Absorption Spectroscopy

    Frankær, Christian Grundahl; Raffalt, Anders Christer; Ståhl, Kenny

    2014-01-01

    Strontium has recently been introduced as a pharmacological agent for the treatment and prevention of osteoporosis. We determined the localization of strontium incorporated into bone matrix from dogs treated with Sr malonate by X-ray absorption spectroscopy. A new approach for analyzing the X......-ray absorption spectra resulted in a compositional model and allowed the relative distribution of strontium in the different bone components to be estimated. Approximately 35–45 % of the strontium present is incorporated into calcium hydroxyapatite (CaHA) by substitution of some of the calcium ions occupying...... highly ordered sites, and at least 30 % is located at less ordered sites where only the first solvation shell is resolved, suggesting that strontium is sur- rounded by only oxygen atoms similar to Sr2? in solution. Strontium was furthermore shown to be absorbed in collagen in which it obtains a higher...

  16. Space Launch System Base Heating Test: Tunable Diode Laser Absorption Spectroscopy

    Parker, Ron; Carr, Zak; MacLean, Matthew; Dufrene, Aaron; Mehta, Manish

    2016-01-01

    This paper describes the Tunable Diode Laser Absorption Spectroscopy (TDLAS) measurement of several water transitions that were interrogated during a hot-fire testing of the Space Launch Systems (SLS) sub-scale vehicle installed in LENS II. The temperature of the recirculating gas flow over the base plate was found to increase with altitude and is consistent with CFD results. It was also observed that the gas above the base plate has significant velocity along the optical path of the sensor at the higher altitudes. The line-by-line analysis of the H2O absorption features must include the effects of the Doppler shift phenomena particularly at high altitude. The TDLAS experimental measurements and the analysis procedure which incorporates the velocity dependent flow will be described.

  17. Measurement of exhaled nitric oxide in beef cattle using tunable diode laser absorption spectroscopy

    Roller, C. B.; Holland, B. P.; McMillen, G.; Step, D. L.; Krehbiel, C. R.; Namjou, K.; McCann, P. J.

    2007-03-01

    Measurement of nitric oxide (NO) in the expired breath of crossbred calves received at a research facility was performed using tunable diode laser absorption spectroscopy. Exhaled NO (eNO) concentrations were measured using NO absorption lines at 1912.07 cm-1 and employing background subtraction. The lower detection limit and measurement precision were determined to be ˜330 parts in 1012 per unit volume. A custom breath collection system was designed to collect lower airway breath of spontaneously breathing calves while in a restraint chute. Breath was collected and analyzed from calves upon arrival and periodically during a 42 day receiving period. There was a statistically significant relationship between eNO, severity of bovine respiratory disease (BRD) in terms of number of times treated, and average daily weight gain over the first 15 days postarrival. In addition, breathing patterns and exhaled CO2 showed a statistically significant relationship with BRD morbidity.

  18. Reconstruction of an excited-state molecular wave packet with attosecond transient absorption spectroscopy

    Cheng, Yan; Chini, Michael; Wang, Xiaowei; González-Castrillo, Alberto; Palacios, Alicia; Argenti, Luca; Martín, Fernando; Chang, Zenghu

    2016-08-01

    Attosecond science promises to allow new forms of quantum control in which a broadband isolated attosecond pulse excites a molecular wave packet consisting of a coherent superposition of multiple excited electronic states. This electronic excitation triggers nuclear motion on the molecular manifold of potential energy surfaces and can result in permanent rearrangement of the constituent atoms. Here, we demonstrate attosecond transient absorption spectroscopy (ATAS) as a viable probe of the electronic and nuclear dynamics initiated in excited states of a neutral molecule by a broadband vacuum ultraviolet pulse. Owing to the high spectral and temporal resolution of ATAS, we are able to reconstruct the time evolution of a vibrational wave packet within the excited B'Σ1u+ electronic state of H2 via the laser-perturbed transient absorption spectrum.

  19. Femtosecond X-ray Absorption Spectroscopy at a Hard X-ray Free Electron Laser

    Lemke, Henrik T.; Bressler, Christian; Chen, Lin X.;

    2013-01-01

    X-ray free electron lasers (XFELs) deliver short (<100 fs) and intense (similar to 10(12) photons) pulses of hard X-rays, making them excellent sources for time-resolved studies. Here we show that, despite the inherent instabilities of current (SASE based) XFELs, they can be used for measuring high......-quality X-ray absorption data and we report femtosecond time-resolved X-ray absorption near-edge spectroscopy (XANES) measurements of a spin-crossover system, iron(II) tris(2,2'-bipyridine) in water. The data indicate that the low-spin to high-spin transition can be modeled by single-exponential kinetics...

  20. Laser plasma x-ray source for ultrafast time-resolved x-ray absorption spectroscopy

    L. Miaja-Avila

    2015-03-01

    Full Text Available We describe a laser-driven x-ray plasma source designed for ultrafast x-ray absorption spectroscopy. The source is comprised of a 1 kHz, 20 W, femtosecond pulsed infrared laser and a water target. We present the x-ray spectra as a function of laser energy and pulse duration. Additionally, we investigate the plasma temperature and photon flux as we vary the laser energy. We obtain a 75 μm FWHM x-ray spot size, containing ∼106 photons/s, by focusing the produced x-rays with a polycapillary optic. Since the acquisition of x-ray absorption spectra requires the averaging of measurements from >107 laser pulses, we also present data on the source stability, including single pulse measurements of the x-ray yield and the x-ray spectral shape. In single pulse measurements, the x-ray flux has a measured standard deviation of 8%, where the laser pointing is the main cause of variability. Further, we show that the variability in x-ray spectral shape from single pulses is low, thus justifying the combining of x-rays obtained from different laser pulses into a single spectrum. Finally, we show a static x-ray absorption spectrum of a ferrioxalate solution as detected by a microcalorimeter array. Altogether, our results demonstrate that this water-jet based plasma source is a suitable candidate for laboratory-based time-resolved x-ray absorption spectroscopy experiments.

  1. Absorption spectroscopy of oxygen, carbon dioxide and water species for applications in combustion diagnostics

    Mei, Anhua

    Laser absorption spectroscopy has been a useful tool applied in combustion diagnostics because of its capability to measure the species' concentration, particularly to measure concentration, temperature, and pressure simultaneously. These measurements provide the necessary information for dynamic combustion control. Due to its advantages such as fast response, non-intrusive nature and applicability under harsh environment like high temperature and high pressure, absorption laser spectroscopy makes it possible to monitor combustion system on-line and in situ. Since its development for more than thirty years, laser spectroscopy has matured, and the novel and advanced laser sensors have pushed it to be applied fast. On the other hand, industry still needs cheaper and more operable spectroscopy, which becomes an important consideration in the development and application of modern laser spectroscopy. This study presents an instrumental structure including the algorithm of the spectrum computation and the hardware configuration. The algorithm applied the central maximum value of the spectrum to simplify the computation. The whole calculation was done extensively using Beer-Lambert theory and HITRAN database which makes it efficient and applicable. This research conducted the simulations of high temperature species, such as CO2, H2O to carry out the algorithm, which were compared with published data. Also, this research designed and performed the experiments of measuring oxygen and its mixture with Helium by using a 760 nm diode laser and a 655 nm Helium/Neon laser sensor with fixed wavelength structures. The results of this research also conclude the following: (1) extensive literature survey, field research and laboratory work; (2) studying the significant theories and experimental methods of the laser spectroscopy; (3) developing efficient and simplified algorithm for spectrum calculation; (4) simulating high temperature species H2O and CO2; (5) designing and building

  2. Vacuum UV broad-band absorption spectroscopy: a powerful diagnostic tool for reactive plasma monitoring

    Cunge, G; Fouchier, M; Brihoum, M; Bodart, P.; Touzeau, M.; N. Sadeghi

    2011-01-01

    Abstract Broad band UV-visible absorption spectroscopy is widely used to measure the concentration of radicals in reactive plasmas. We extended the applicability of this technique to the VUV (115 nm to 200 nm), the spectral range in which the electronic transitions from the ground state to the Rydberg or pre-dissociated states of many closed shell molecules are located. This gives access to the absolute densities of species which do not, or weakly absorb in the UV/visible range. The techni...

  3. Behaviors of harmonic signals in wavelength-modulated spectroscopy under high absorption strength

    Yuntao Wang; Haiwen Cai; Jianxin Geng; Zhengqing Pan; Dijun Chen; Zujie Fang

    2007-01-01

    @@ Behaviors of harmonic signals in wavelength modulation spectroscopy (WMS) for gas detection with Lorentzian line under high absorption strength are investigated. Approximate analytic expressions of the second, fourth, and sixth harmonics on the strength are presented in concise forms. Simulations show that the expressions are in agreement with the Fourier expansion by numerical integration. It is expected theoretically and experimentally in a WMS system for methane detection that there are not only a maximum, but also a null point in the harmonics versus strength relations, which should be of practical importance in methane sensing applications.

  4. Femtosecond Transient Absorption Spectroscopy on the Light-Adaptation of Living Plants

    Müller, M. G.; Jahns, P.; Holzwarth, A. R.

    2013-03-01

    The photoprotection reaction of the photosynthetic system under excessive sun light has been resolved for the first time by femtosecond absorption spectroscopy from the visible to near-infrared in intact leaves of Arabidopsis thaliana. The light-adaptation process was measured and a prominent non-photochemical quenching (npq) behavior located in photosystem II was observed. Among the various npq quenching mechanisms which have been discussed so far the most likely is the formation of chlorophyll-chlorophyll charge-transfer states which create a powerful energy dissipation pathway for the quenching.

  5. Quantum Cascade Laser Absorption Spectroscopy as a Plasma Diagnostic Tool: An Overview

    Jürgen Röpcke

    2010-07-01

    Full Text Available The recent availability of thermoelectrically cooled pulsed and continuous wave quantum and inter-band cascade lasers in the mid-infrared spectral region has led to significant improvements and new developments in chemical sensing techniques using in-situ laser absorption spectroscopy for plasma diagnostic purposes. The aim of this article is therefore two-fold: (i to summarize the challenges which arise in the application of quantum cascade lasers in such environments, and, (ii to provide an overview of recent spectroscopic results (encompassing cavity enhanced methods obtained in different kinds of plasma used in both research and industry.

  6. Quantum Cascade Laser Absorption Spectroscopy as a Plasma Diagnostic Tool: An Overview

    Welzel, Stefan; Hempel, Frank; Hübner, Marko; Lang, Norbert; Davies, Paul B.; Röpcke, Jürgen

    2010-01-01

    The recent availability of thermoelectrically cooled pulsed and continuous wave quantum and inter-band cascade lasers in the mid-infrared spectral region has led to significant improvements and new developments in chemical sensing techniques using in-situ laser absorption spectroscopy for plasma diagnostic purposes. The aim of this article is therefore two-fold: (i) to summarize the challenges which arise in the application of quantum cascade lasers in such environments, and, (ii) to provide an overview of recent spectroscopic results (encompassing cavity enhanced methods) obtained in different kinds of plasma used in both research and industry. PMID:22163581

  7. 30% improvement in absorption spectroscopy detectivity achieved by the detuned loading of a quantum cascade laser.

    Michel, Florian; Juretzka, Carsten; Carras, Mathieu; Elsäßer, Wolfgang

    2014-11-01

    We perform a direct absorption spectroscopy experiment of carbon monoxide at 2193  cm(-1) by exploring the detectivity improvement potential of an intensity noise (IN)-reduced distributed feedback (DFB) quantum cascade laser. This was achieved by a detuned loading approach via a short, phase-sensitive optical feedback cavity. Under optimum IN reduction conditions, we obtain an improvement in signal-to-noise ratio from 733 to 1048, which transfers into a detection limit improvement from 1.2 ppm to 840 ppb. Therefore, we achieve a 30% lower detection limit, with the IN reduced when compared to the free-running case. PMID:25361352

  8. Laser plasma x-ray source for ultrafast time-resolved x-ray absorption spectroscopy

    Miaja-Avila, L.; G. C. O'Neil; Uhlig, J.; C. L. Cromer; Dowell, M. L.; Jimenez, R.; Hoover, A. S.; Silverman, K. L.; Ullom, J. N.

    2015-01-01

    We describe a laser-driven x-ray plasma source designed for ultrafast x-ray absorption spectroscopy. The source is comprised of a 1 kHz, 20 W, femtosecond pulsed infrared laser and a water target. We present the x-ray spectra as a function of laser energy and pulse duration. Additionally, we investigate the plasma temperature and photon flux as we vary the laser energy. We obtain a 75 μm FWHM x-ray spot size, containing ∼106 photons/s, by focusing the produced x-rays with a polycapillary opti...

  9. Two attosecond pulse transient absorption spectroscopy and extraction of the instantaneous AC Stark shift in helium

    Bækhøj, Jens E.; Bojer Madsen, Lars

    2016-07-01

    In two attosecond pulse absorption spectroscopy (TAPAS) the use of two attosecond XUV pulses allows the extraction of atomic and molecular quantum mechanical dipole phases from spectroscopic measurements. TAPAS relies on interference between processes that individually only include a single XUV photon, and therefore does not rely on high intensity attosecond pulses. To show the usefulness and limitations of the TAPAS method we investigate its capability of capturing the instantaneous AC Stark shift induced by a midinfrared 3200 nm pulse in the | 1{{s}}2{{p}}> state of helium.

  10. Picosecond X-ray absorption spectroscopy: application to coordination chemistry compounds in solution

    Saes, Melanie

    2004-01-01

    The photocycle of aqueous ruthenium-(trisbipyridine) [Ru(bpy)3]2+ was studied under high laser excitation intensities and high sample concentrations with picosecond resolved x-ray absorption spectroscopy. In a pump-probe scheme a femtosecond laser pulse promotes a 4d electron from the ruthenium to the ligand orbitals, thus creating a metal-to-ligand-charge-transfer (MLCT) complex. A hard x-ray pulse from a synchrotron source probes the ruthenium L3 and L2 edges, monitoring the electronic and ...

  11. Picosecond X-ray absorption spectroscopy: application to coordination chemistry compounds in solution

    Saes, Melanie; Chergui, Majed

    2005-01-01

    The photocycle of aqueous ruthenium-(trisbipyridine) [Ru(bpy)3]2+ was studied under high laser excitation intensities and high sample concentrations with picosecond resolved x-ray absorption spectroscopy. In a pump-probe scheme a femtosecond laser pulse promotes a 4d electron from the ruthenium to the ligand orbitals, thus creating a metal-to-ligand-charge-transfer (MLCT) complex. A hard x-ray pulse from a synchrotron source probes the ruthenium L3 and L2 edges, monitoring the electronic and ...

  12. Optical Absorption and Raman Spectroscopy Study of the Fluorinated Double-Wall Carbon Nanotubes

    Gevko, Pavel N.; Bulusheva, Lyubov Gennadievna; Okotrub, Alexander Vladimirovich; Yudanov, Nikolay Fedorovich; Yushina, I. V.; Grachev, K. A.; Pugachev, A. M.; Surovtsev, N. V.; Flahaut, Emmanuel

    2006-01-01

    Double-wall carbon nanotube (DWNT) samples have been fluorinated at room temperature with varied concentration of a fluorinating agent BrF3. Content of the products estimated from X-ray photoelectron data was equal to CF0.20 and CF0.29 in the case of deficit and excess of BrF3. Raman spectroscopy showed considerable decrease of carbon nanotube amount in the fluorinated samples. Analysis of optical absorption spectra measured for pristine and fluorinated DWNT samples revealed a selectivity of ...

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

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

    1995-12-01

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

  14. A quality control technique based on UV-VIS absorption spectroscopy for tequila distillery factories

    Barbosa Garcia, O.; Ramos Ortiz, G.; Maldonado, J. L.; Pichardo Molina, J.; Meneses Nava, M. A.; Landgrave, Enrique; Cervantes, M. J.

    2006-02-01

    A low cost technique based on the UV-VIS absorption spectroscopy is presented for the quality control of the spirit drink known as tequila. It is shown that such spectra offer enough information to discriminate a given spirit drink from a group of bottled commercial tequilas. The technique was applied to white tequilas. Contrary to the reference analytic methods, such as chromatography, for this technique neither special personal training nor sophisticated instrumentations is required. By using hand-held instrumentation this technique can be applied in situ during the production process.

  15. Utilization of synchrotron radiation in analytical chemistry. Hard X-ray emission and absorption spectroscopy

    This paper takes up X-ray absorption fine structure (XAFS) method, which has widely spread due to the energy selectivity of radiation, and fluorescent X-ray spectroscopy, which is utilized in non-destructive screening analysis and high precision quantitative analysis method for bulk materials due to the popularity of commercialized devices that usually use X-ray sources, and explains their devices, measurement principle, and applications. As the device, it introduces X-ray fluorescence spectrometer that was installed in SPring-8 beamline (BL05SS). As the application examples of fluorescent X-ray spectroscopy, it introduces the analysis of heavy elements due to high-energy X-ray excitation, and fluorescent X-ray analysis using microbeams. As the example of the use of XAFS method, it introduces the in-situ observation of the charging/discharging process of lithium battery. (A.O.)

  16. Microscale X-ray Absorption Spectroscopy on the GSECARS Sector 13 at the APS

    Stephen-Sutto

    2000-01-01

    GeoSoilEnviroCARS (GSECARS) is a national user facility for frontier research in the earth sciences using synchrotrons radiation at the Advanced Photon Source, Argonne National Laboratory. GSECARS provides earth scientists with access to the high-brilliance hard x-rays from this third-generation synchrotrons light source. The research conducted at this facility will advance our knowledge of the composition, structure and properties of earth materials, the processes they control and the processes that produce them. All principal synchrotron-based analytical techniques in demand by earth scientists are being brought to bear on earth science problems: (1) high-pressure/high-temperature crystallography and spectroscopy using the diamond anvil cell; (2) high-pressure/high-temperature crystallography using the large-volume press; (3) powder, single crystal and interface diffraction; (4) x-ray absorption fine structure (XAFS) spectroscopy; (5) x-ray fluorescence microprobe analysis and microspectroscopy; and (6) mic...

  17. IDENTIFICATION OF ADULTERANT AND ALCOHOL ROUTE IN BIODIESEL USING MID-INFRARED ABSORPTION SPECTROSCOPY

    Maryleide Ventura da Silva

    2014-01-01

    Full Text Available Mid-infrared absorption spectroscopy was used to analyze soybean oil, ethylic and methylic soybean biodiesel, and blends prepared with soybean oil mixed with biodiesel, in order to evaluate this method as an alternative to assess oil as impurities or adulterant in biodiesel. We also aimed to determine whether the biodiesel was prepared by the ethyl or methyl routes, by inspecting the infrared spectra. The C-O functional groups between 1100 and 1200 cm-1 are different for oil and biodiesel, which allows them to be used to distinguish impurities (residual oil in biofuel. The peak C-O-C at 1017 cm-1 is characteristic for methylic biodiesel, and the peak O-C-C at 1035 cm-1 for ethylic biodiesel. These vibrational modes can therefore be used to indicate the route used to prepare the biofuel. Results indicated that infrared spectroscopy is appropriate for monitoring the quality of biofuel for commercial sale.

  18. Investigation of titanium germanide formation by Raman scattering and x-ray absorption spectroscopy

    This paper reports on the reactions of titanium on germanium that were studied using Raman spectroscopy and X-ray Absorption Spectroscopy (XAS). Samples used in this study were produced in a custom MBE system with dual E-gun sources, two filament sources, and base pressure -10 Torr. Ge(100) substrates were prepared by chemical cleaning and homoepitaxial deposition of 500 Angstrom--1000 Angstrom Ge at 550 degrees C. Ti was deposited and subsequently annealed at 50 degrees C intervals from 500 degrees C to 700 degrees C. Raman and XANES spectra of the titanium germanides were obtained and used to examine the evolution of the crystalline structures which form by the interface reactions of Ti on Ge. low-order phase formed by diffusion controlled growth prior to the formation of TiGe2 (isomorphous with TiSi2 [C54]) by nucleation controlled growth

  19. In situ characterization of few-cycle laser pulses in transient absorption spectroscopy

    Blättermann, Alexander; Kaldun, Andreas; Ding, Thomas; Stooß, Veit; Laux, Martin; Rebholz, Marc; Pfeifer, Thomas

    2016-01-01

    Attosecond transient absorption spectroscopy has thus far been lacking the capability to simultaneously characterize the intense laser pulses at work within a time-resolved quantum-dynamics experiment. However, precise knowledge of these pulses is key to extracting quantitative information in strong-field highly nonlinear light-matter interactions. Here, we introduce and experimentally demonstrate an ultrafast metrology tool based on the time-delay-dependent phase shift imprinted on a strong-field driven resonance. Since we analyze the signature of the laser pulse interacting with the absorbing spectroscopy target, the laser pulse duration and intensity are determined in situ. As we also show, this approach allows for the quantification of time-dependent bound-state dynamics in one and the same experiment. In the future, such experimental data will facilitate more precise tests of strong-field dynamics theories.

  20. A Complete Overhaul of the Electron Energy-Loss Spectroscopy and X-Ray Absorption Spectroscopy Database: eelsdb.eu.

    Ewels, Philip; Sikora, Thierry; Serin, Virginie; Ewels, Chris P; Lajaunie, Luc

    2016-06-01

    The electron energy-loss spectroscopy (EELS) and X-ray absorption spectroscopy (XAS) database has been completely rewritten, with an improved design, user interface, and a number of new tools. The database is accessible at https://eelsdb.eu/ and can now be used without registration. The submission process has been streamlined to encourage spectrum submissions and the new design gives greater emphasis on contributors' original work by highlighting their papers. With numerous new filters and a powerful search function, it is now simple to explore the database of several hundred EELS and XAS spectra. Interactive plots allow spectra to be overlaid, facilitating online comparison. An application-programming interface has been created, allowing external tools and software to easily access the information held within the database. In addition to the database itself, users can post and manage job adverts and read the latest news and events regarding the EELS and XAS communities. In accordance with the ongoing drive toward open access data increasingly demanded by funding bodies, the database will facilitate open access data sharing of EELS and XAS spectra. PMID:26899024

  1. X-ray absorption spectroscopy investigation of structurally modified lithium niobate crystals

    Vitova, Tonya

    2008-02-15

    The type and concentration of impurity centers in different valence states are crucial for tuning the photorefractive properties of doped Lithium Niobate (LN) crystals. X-ray Absorption Spectroscopy (XAS) is an appropriate tool for studying the local structure of impurity centers. XAS combined with absorption in UV/VIS/IR and High Resolution X-ray Emission Spectroscopy (HRXES) provide information about the valence state of the dopant ions in as-grown, reduced or oxidized doped LN crystals. Cu (Cu{sup 1+} and Cu{sup 2+}) and Fe (Fe{sup 2+} and Fe{sup 3+}) atoms are found in two different valence states, whereas there are indications for a third Mn valency, in addition to Mn{sup 2+} and Mn{sup 3+} in manganese-doped LN crystals. One of the charge compensation mechanisms during reduction of copper- doped LN crystals is outgassing of oxygen atoms. Cu ions in the reduced crystals have at least two different site symmetries: twofold (Cu{sup 1+}) and sixfold (Cu{sup 2+}) coordinated by O atoms. Fe and Mn atoms are coordinated by six O atoms. Cu and Fe ions are found to occupy only Li sites, whereas Mn ions are also incorporated into Li and Nb sites. The refractive index change in LN crystals irradiated with {sup 3}He{sup 2+} ions is caused by structurally disordered centers, where Nb atoms are displaced from normal crystallographic sites and Li or/and O vacancies are present. (orig.)

  2. X-ray absorption spectroscopy investigation of structurally modified lithium niobate crystals

    The type and concentration of impurity centers in different valence states are crucial for tuning the photorefractive properties of doped Lithium Niobate (LN) crystals. X-ray Absorption Spectroscopy (XAS) is an appropriate tool for studying the local structure of impurity centers. XAS combined with absorption in UV/VIS/IR and High Resolution X-ray Emission Spectroscopy (HRXES) provide information about the valence state of the dopant ions in as-grown, reduced or oxidized doped LN crystals. Cu (Cu1+ and Cu2+) and Fe (Fe2+ and Fe3+) atoms are found in two different valence states, whereas there are indications for a third Mn valency, in addition to Mn2+ and Mn3+ in manganese-doped LN crystals. One of the charge compensation mechanisms during reduction of copper- doped LN crystals is outgassing of oxygen atoms. Cu ions in the reduced crystals have at least two different site symmetries: twofold (Cu1+) and sixfold (Cu2+) coordinated by O atoms. Fe and Mn atoms are coordinated by six O atoms. Cu and Fe ions are found to occupy only Li sites, whereas Mn ions are also incorporated into Li and Nb sites. The refractive index change in LN crystals irradiated with 3He2+ ions is caused by structurally disordered centers, where Nb atoms are displaced from normal crystallographic sites and Li or/and O vacancies are present. (orig.)

  3. Characterization of the Pore Filling of Solid State Dye Sensitized Solar Cells with Photoinduced Absorption Spectroscopy

    Carol Olson

    2011-01-01

    Full Text Available Near steady-state photoinduced absorption (PIA and UV-Vis absorption spectroscopy are used to characterize the pore filling of spiro-MeOTAD (2,2′,7,7′-tetrakis-(N,N-di-p-methoxyphenylamine9,9′-spirobifluorene into the nanoparticulate TiO2 electrode of a solid-state dye-sensitized solar cell (ssDSC. The volumetric ratio of filled to unfilled pore volumes, as well as the optical signature of interacting chemical species, that is, the hole-transfer yield (HTY, are investigated. PIA spectroscopy is used to measure the HTY, relative to the amount of spiro-MeOTAD present, without needing to determine the extinction coefficients of the dye and spiro-MeOTAD cation species. The Beer-Lambert law is used to relate the relative PIA signal to the penetration length of the hole-conductor in the TiO2 film. For the sample thickness range of 1.4–5 μm investigated here, the optimum characteristic penetration length is determined to be 3.1+0.46 μm, which is compared to 1.4 μm for the 200 mg mL−1 concentration of spiro-MeOTAD conventionally used. Therefore, doubling the effective penetration of spiro-MeOTAD is necessary to functionalize all the dye molecules in a ssDSC.

  4. X-ray absorption spectroscopy on magnetic nanoscale systems for modern applications.

    Schmitz-Antoniak, Carolin

    2015-06-01

    X-ray absorption spectroscopy facilitated by state-of-the-art synchrotron radiation technology is presented as a powerful tool to study nanoscale systems, in particular revealing their static element-specific magnetic and electronic properties on a microscopic level. A survey is given on the properties of nanoparticles, nanocomposites and thin films covering a broad range of possible applications. It ranges from the ageing effects of iron oxide nanoparticles in dispersion for biomedical applications to the characterisation on a microscopic level of nanoscale systems for data storage devices. In this respect, new concepts for electrically addressable magnetic data storage devices are highlighted by characterising the coupling in a BaTiO(3)/CoFe(2)O(4) nanocomposite as prototypical model system. But classical magnetically addressable devices are also discussed on the basis of tailoring the magnetic properties of self-assembled ensembles of FePt nanoparticles for data storage and the high-moment material Fe/Cr/Gd for write heads. For the latter cases, the importance is emphasised of combining experimental approaches in x-ray absorption spectroscopy with density functional theory to gain a more fundamental understanding. PMID:26029938

  5. Novel focal point multipass cell for absorption spectroscopy on small sized atmospheric pressure plasmas

    Winter, Jörn; Hänel, Mattis; Reuter, Stephan

    2016-04-01

    A novel focal point multipass cell (FPMPC) was developed, in which all laser beams propagate through a common focal point. It is exclusively constructed from standard optical elements. Main functional elements are two 90∘ off-axis parabolic mirrors and two retroreflectors. Up to 17 laser passes are demonstrated with a near-infrared laser beam. The number of laser passes is precisely adjustable by changing the retroreflector distance. At the focal point beams are constricted to fit through an aperture of 0.8 mm. This is shown for 11 beam passes. Moreover, the fast temporal response of the cell permits investigation of transient processes with frequencies up to 10 MHz. In order to demonstrate the applicability of the FPMPC for atmospheric pressure plasma jets, laser absorption spectroscopy on the lowest excited argon state (1s5) was performed on a 1 MHz argon atmospheric pressure plasma jet. From the obtained optical depth profiles, the signal-to-noise ratio was deduced. It is shown that an elevation of the laser pass number results in an proportional increase of the signal-to-noise ratio making the FPMPC an appropriate tool for absorption spectroscopy on plasmas of small dimensions.

  6. Time-resolved absorption spectroscopy of optically pumped Si by using fs-laser plasma x-ray

    Femtosecond laser-produced plasmas emit ultrashort x-ray pulse that is synchronized to a femtosecond laser pulse. By utilizing this feature, we demonstrated time-resolved soft x-ray absorption measurements of optically pumped silicon near its LII,III absorption edge by means of pump-probe spectroscopy. As a result, we observed more than 10% increase in the absorption near absorption edge caused by laser pulse irradiation, which means that the transition of core-electrons was rapidly modified by excitation of valence electrons. The recovery time constant of this change was measure to be about 20 ps. (author)

  7. The Optical Absorption Coefficient of Bean Seeds Investigated Using Photoacoustic Spectroscopy

    Sanchez-Hernandez, G.; Hernandez-Aguilar, C.; Dominguez-Pacheco, A.; Cruz-Orea, A.; Perez-Reyes, M. C. J.; Martinez, E. Moreno

    2015-06-01

    A knowledge about seed optical parameters is of great relevance in seed technology practice. Such parameters provide information about its absorption and reflectance, which could be useful for biostimulation processes, by light sources, in early stages of seed germination. In the present research photoacoustic spectroscopy (PAS) and the Rosencwaig and Gersho model were used to determine the optical absorption coefficient () of five varieties of bean seeds ( Phaseolus vulgaris L.), of different productive cycles; the seeds were biostimulated by laser treatment to evaluate the effects of biostimulation pre-sowing. It was found that the bean varieties V1, V2, V4, and V5 were optically opaque in the visible spectrum; in the case of the V3 variety, this sample was optically transparent from 680 nm. The varieties of the studied bean seeds showed significant statistical differences in sizes and also in their optical absorption spectra. The biostimulation effects showed that the seed samples with a higher optical penetration length had a positive biostimulation, in the percentage of germination, obtaining an enhancement of 47 % compared to the control sample. The utility of PAS for the optical characterization of seeds has been demonstrated in this study of the laser biostimulation process of this kind of samples.

  8. Initial Results of Optical Vortex Laser Absorption Spectroscopy in the HYPER-I Device

    Yoshimura, Shinji; Asai, Shoma; Aramaki, Mitsutoshi; Terasaka, Kenichiro; Ozawa, Naoya; Tanaka, Masayoshi; Morisaki, Tomohiro

    2015-11-01

    Optical vortex beams have a potential to make a new Doppler measurement, because not only parallel but perpendicular movement of atoms against the beam axis causes the Doppler shift of their resonant absorption frequency. As the first step of a proof-of-principle experiment, we have performed the optical vortex laser absorption spectroscopy for metastable argon neutrals in an ECR plasma produced in the HYPER-I device at the National Institute for Fusion Science, Japan. An external cavity diode laser (TOPTICA, DL100) of which center wavelength was 696.735 nm in vacuum was used for the light source. The Hermite-Gaussian (HG) beam was converted into the Laguerre-Gaussian (LG) beam (optical vortex) by a computer-generated hologram displayed on the spatial light modulator (Hamamatsu, LCOS-SLM X10468-07). In order to make fast neutral flow across the LG beam, a high speed solenoid valve system was installed on the HYPER-I device. Initial results including the comparison of absorption spectra for HG and LG beams will be presented. This study was supported by NINS young scientists collaboration program for cross-disciplinary study, NIFS collaboration research program (NIFS13KOAP026), and JSPS KAKENHI grant number 15K05365.

  9. Broadband fitting approach for the application of supercontinuum broadband laser absorption spectroscopy to combustion environments

    Göran Blume, Niels; Ebert, Volker; Dreizler, Andreas; Wagner, Steven

    2016-01-01

    In this work, a novel broadband fitting approach for quantitative in-flame measurements using supercontinuum broadband laser absorption spectroscopy (SCLAS) is presented. The application and verification of this approach in an atmospheric, laminar, non-premixed CH4/air flame (Wolfhard-Parker burner, WHP) is discussed. The developed fitting scheme allows for an automatic recognition and fitting of a B-spline curve reference intensity for SCLAS broadband measurements while automatically removing the influence of absorption peaks. This approach improves the fitting residual locally (in between absorption lines) and globally by 23% and 13% respectively, while improving the in-flame SNR by a factor of 2. Additionally, the approach inherently improves the time-wavelength-correlation based on recorded in-flame measurements itself in combination with a theoretical spectrum of the analyte. These improvements have allowed for the recording of complete spatially resolved methane concentration profiles in the WHP burner. Comparison of the measured absolute mole fraction profile for methane with previously measured reference data shows excellent agreement in position, shape and absolute values. These improvements are a prerequisite for the application of SCLAS in high-pressure combustion systems.

  10. A new flexible monochromator setup for quick scanning x-ray absorption spectroscopy

    A new monochromator setup for quick scanning x-ray absorption spectroscopy in the subsecond time regime is presented. Novel driving mechanics allow changing the energy range of the acquired spectra by remote control during data acquisition for the first time, thus dramatically increasing the flexibility and convenience of this method. Completely new experiments are feasible due to the fact that time resolution, edge energy, and energy range of the acquired spectra can be changed continuously within seconds without breaking the vacuum of the monochromator vessel and even without interrupting the measurements. The advanced mechanics are explained in detail and the performance is characterized with x-ray absorption spectra of pure metal foils. The energy scale was determined by a fast and accurate angular encoder system measuring the Bragg angle of the monochromator crystal with subarcsecond resolution. The Bragg angle range covered by the oscillating crystal can currently be changed from 0 deg. to 3.0 deg. within 20 s, while the mechanics are capable to move with frequencies of up to ca. 35 Hz, leading to ca. 14 ms/spectrum time resolution. A new software package allows performing programmed scan sequences, which enable the user to measure stepwise with alternating parameters in predefined time segments. Thus, e.g., switching between edges scanned with the same energy range is possible within one in situ experiment, while also the time resolution can be varied simultaneously. This progress makes the new system extremely user friendly and efficient to use for time resolved x-ray absorption spectroscopy at synchrotron radiation beamlines.

  11. Microscale X-ray Absorption Spectroscopy on the GSECARS Sector 13 at the APS

    GeoSoilEnviroCARS (GSECARS) is a national user facility for frontier research in the earth sciences using synchrotrons radiation at the Advanced Photon Source, Argonne National Laboratory. GSECARS provides earth scientists with access to the high-brilliance hard x-rays from this third-generation synchrotrons light source. The research conducted at this facility will advance our knowledge of the composition, structure and properties of earth materials, the processes they control and the processes that produce them. All principal synchrotron-based analytical techniques in demand by earth scientists are being brought to bear on earth science problems: (1) high-pressure/high-temperature crystallography and spectroscopy using the diamond anvil cell; (2) high-pressure/high-temperature crystallography using the large-volume press; (3) powder, single crystal and interface diffraction; (4) x-ray absorption fine structure (XAFS) spectroscopy; (5) x-ray fluorescence microprobe analysis and microspectroscopy; and (6) microtomography. This grant supported the design and construction of dedicated microspectroscopy instrumentation (x-ray absorption fine structure (XAFS) spectroscopy techniques, e.g., EXAFS and XANES, applied with ∼ micrometer spatial resolution) as part of the GeoSoilEnviroCARS national user facility. This new APS instrumentation offers dramatically improved capabilities over existing facilities in terms of spatial resolution and elemental sensitivity. MicroXAFS is essential in cases where sample size is limited (such as fluid inclusions in minerals, fine-grained minerals and samples in diamond anvil, high pressure cells) and/or chemical speciation is heterogeneous (fine-grained, polymineralic sediments and rocks, zoned crystals, and products of non-equilibrium reactions). The new instrumentation is applicable to studies of hydrothermal fluid processes, migration and encapsulation of toxic and radioactive wastes, for example. The availability of quantitative

  12. Absorption spectroscopy characterization measurements of a laser-produced Na atomic beam

    Ching, C.H.; Bailey, J.E.; Lake, P.W.; Filuk, A.B.; Adams, R.G.; McKenney, J.

    1996-06-01

    This work describes a pulsed Na atomic beam source developed for spectroscopic diagnosis of a high-power ion diode on the Particle Beam Fusion Accelerator II. The goal is to produce a {approximately} 10{sup 12}-cm{sup {minus}3}-density Na atomic beam that can be injected into the diode acceleration gap to measure electric and magnetic fields from the Stark and Zeeman effects through laser-induced-fluorescence or absorption spectroscopy. A {approximately} 10 ns fwhm, 1.06 {micro}m, 0.6 J/cm{sup 2} laser incident through a glass slide heats a Na-bearing thin film, creating a plasma that generates a sodium vapor plume. A {approximately} 1 {micro}sec fwhm dye laser beam tuned to 5,890 {angstrom} is used for absorption measurement of the Na I resonant doublet by viewing parallel to the film surface. The dye laser light is coupled through a fiber to a spectrograph with a time-integrated CCD camera. A two-dimensional mapping of the Na vapor density is obtained through absorption measurements at different spatial locations. Time-of-flight and Doppler broadening of the absorption with {approximately} 0.1 {angstrom} spectral resolution indicate that the Na neutral vapor temperature is about 0.5 to 2 eV. Laser-induced-fluorescence from {approximately} 1 {times} 10{sup 12}-cm{sup {minus}3} Na I 3s-3p lines observed with a streaked spectrograph provides a signal level sufficient for {approximately} 0.06 {angstrom} wavelength shift measurements in a mock-up of an ion diode experiment.

  13. Pump-flow-probe x-ray absorption spectroscopy as a tool for studying aintermediate states of photocatalytic systems

    Smolentsev, Grigory; Guda, Alexander; Zhang, Xiaoyi;

    2013-01-01

    A new setup for pump-flow-probe X-ray absorption spectroscopy has been implemented at the SuperXAS beamline of the Swiss Light Source. It allows recording X-ray absorption spectra with a time resolution of tens of microseconds and high detection efficiency for samples with sub-millimolar concentr......A new setup for pump-flow-probe X-ray absorption spectroscopy has been implemented at the SuperXAS beamline of the Swiss Light Source. It allows recording X-ray absorption spectra with a time resolution of tens of microseconds and high detection efficiency for samples with sub...... measurement technique that utilizes a 1 kHz repetition rate laser and multiple X-ray probe pulses. Such an experiment was performed at beamline 11ID-D of the Advanced Photon Source. Advantages, limitations, and potential for improvement of the pump-flow-probe setup are discussed by analyzing the photon...

  14. Double resonant absorption measurement of acetylene symmetric vibrational states probed with cavity ring down spectroscopy

    Karhu, J; Vainio, M; Metsälä, M; Hoekstra, S; Halonen, L

    2016-01-01

    A novel mid-infrared/near-infrared double resonant absorption setup for studying infrared-inactive vibrational states is presented. A strong vibrational transition in the mid-infrared region is excited using an idler beam from a singly resonant continuous-wave optical parametric oscillator, to populate an intermediate vibrational state. High output power of the optical parametric oscillator and the strength of the mid-infrared transition result in efficient population transfer to the intermediate state, which allows measuring secondary transitions from this state with a high signal-to-noise ratio. A secondary, near-infrared transition from the intermediate state is probed using cavity ring down spectroscopy, which provides high sensitivity in this wavelength region. Due to the narrow linewidths of the excitation sources, the rovibrational lines of the secondary transition are measured with sub-Doppler resolution. The setup is used to access a previously unreported symmetric vibrational state of acetylene, $\

  15. Laser absorption spectroscopy diagnostics of helium metastable atoms generated in dielectric barrier discharge cryoplasmas

    Urabe, Keiichiro; Muneoka, Hitoshi; Stauss, Sven; Sakai, Osamu; Terashima, Kazuo

    2015-10-01

    Cryoplasmas, which are plasmas whose gas temperatures are below room temperature (RT), have shown dynamic changes in their physical and chemical characteristics when the gas temperature in the plasmas (Tgp) was decreased from RT. In this study, we measured the temporal behavior of helium metastable (Hem) atoms generated in a parallel-plate dielectric barrier discharge at ambient gas temperatures (Tga) of 300, 100, and 14 K and with a gas density similar to atmospheric conditions by laser absorption spectroscopy. The increments of Tgp to Tga were less than 20 K. We found from the results that the Hem lifetime and maximum density become longer and larger over one order of magnitude for lower Tga. The reasons for the long Hem lifetime at low Tga are decreases in the rate coefficients of three-body Hem quenching reactions and in the amounts of molecular impurities with boiling points higher than that of He.

  16. Optical absorption spectroscopy on a metal-halide high intensity discharge arc lamp using synchrotron radiation

    Bonvallet, G A; Lawler, J E [Department of Physics, University of Wisconsin, 1150 University Avenue, Madison, WI 53706 (United States)

    2003-07-07

    A sensitive, spatially resolved optical absorption spectroscopy experiment using synchrotron radiation on metal-halide high intensity discharge (MH-HID) lamps was performed. This experiment was used to measure the absolute column densities of ground and excited level Sc atoms, ground level Sc{sup +} ions, and ground level Na atoms in a 250 W MH-HID lamp during operation. The column densities were Abel inverted and used to determine the arc temperature as a function of radius and the absolute electron density as a function of radius. Although most of these measurements were made using a one-dimensional spectrally-multiplexed experiment, a two-dimensional spatially and spectrally multiplexed experiment has also been demonstrated. The absolute density and temperature maps from this experiment were used to determine the absolute near-infrared output power from the MH-HID lamp as described in the companion paper (Smith et al 2003)

  17. Time-resolved broadband cavity-enhanced absorption spectroscopy for chemical kinetics.

    Sheps, Leonid; Chandler, David W.

    2013-04-01

    Experimental measurements of elementary reaction rate coefficients and product branching ratios are essential to our understanding of many fundamentally important processes in Combustion Chemistry. However, such measurements are often impossible because of a lack of adequate detection techniques. Some of the largest gaps in our knowledge concern some of the most important radical species, because their short lifetimes and low steady-state concentrations make them particularly difficult to detect. To address this challenge, we propose a novel general detection method for gas-phase chemical kinetics: time-resolved broadband cavity-enhanced absorption spectroscopy (TR-BB-CEAS). This all-optical, non-intrusive, multiplexed method enables sensitive direct probing of transient reaction intermediates in a simple, inexpensive, and robust experimental package.

  18. The application of synchrotron x-ray absorption spectroscopy to problems of industrial heterogeneous catalysis

    A fundamental understanding of catalytic chemistry is valuable for fine-tuning existing processes and for inventing new ones. However, active phases are hard to study, being typically dilute species in amorphous solids comprising many elements. X-ray Absorption Spectroscopy (XAS) can be applied to most catalysts under the appropriate in situ conditions. The ability is unique in observing all the trace elements in the catalysts forming active phases, poisons, and catalysts for unwanted side reactions. Every spectrum contains independent information on the average chemical state, and physical environment, of absorbing atoms. This information can yield new processes, and improvements in existing ones, after the rate of empirical advances in a technology has diminished. The authors discuss XAS studies of metallic and non-metallic components in industrial heterogeneous catalysts. The novel observations made possible by in situ measurement conditions are emphasized

  19. Structure-activity relationships of heterogeneous catalysts from time-resolved X-ray absorption spectroscopy

    Knowing the composition and the evolution of the bulk structure of a heterogeneous catalyst under working conditions (in situ) is a pre-requisite for understanding structure-activity relationships. X-ray absorption spectroscopy can be employed to study a catalytically active material in situ. In addition to steady-state investigations, the technique permits experiments with a time-resolution in the sub-second range to elucidate the solid-state kinetics of the reactions involved. Combined with mass spectrometry, the evolution of the short-range order structure of a heterogeneous catalyst, the average valence of the constituent metals, and the phase composition can be obtained. Here we present results obtained from time-resolved studies on the reduction of MoO3 in propene and in propene and oxygen

  20. X-ray Absorption Spectroscopy Characterization of a Li/S Cell

    Yifan Ye

    2016-01-01

    Full Text Available The X-ray absorption spectroscopy technique has been applied to study different stages of the lithium/sulfur (Li/S cell life cycle. We have investigated how speciation of S in Li/S cathodes changes upon the introduction of CTAB (cetyltrimethylammonium bromide, CH3(CH215N+(CH33Br− and with charge/discharge cycling. The introduction of CTAB changes the synthesis reaction pathway dramatically due to the interaction of CTAB with the terminal S atoms of the polysulfide ions in the Na2Sx solution. For the cycled Li/S cell, the loss of electrochemically active sulfur and the accumulation of a compact blocking insulating layer of unexpected sulfur reaction products on the cathode surface during the charge/discharge processes make the capacity decay. A modified coin cell and a vacuum-compatible three-electrode electro-chemical cell have been introduced for further in-situ/in-operando studies.

  1. Infrared reflection-absorption spectroscopy: principles and applications to lipid-protein interaction in Langmuir films.

    Mendelsohn, Richard; Mao, Guangru; Flach, Carol R

    2010-04-01

    Infrared reflection-absorption spectroscopy (IRRAS) of lipid/protein monolayer films in situ at the air/water interface provides unique molecular structure and orientation information from the film constituents. The technique is thus well suited for studies of lipid/protein interaction in a physiologically relevant environment. Initially, the nature of the IRRAS experiment is described and the molecular structure information that may be obtained is recapitulated. Subsequently, several types of applications, including the determination of lipid chain conformation and tilt as well as elucidation of protein secondary structure are reviewed. The current article attempts to provide the reader with an understanding of the current capabilities of IRRAS instrumentation and the type of results that have been achieved to date from IRRAS studies of lipids, proteins, and lipid/protein films of progressively increasing complexity. Finally, possible extensions of the technology are briefly considered. PMID:20004639

  2. Infra-red absorption spectroscopy of Nd:YAG and Nd:GSGG surface contaminants

    Neodymium doped yttrium aluminum garnet (Nd:YAG) is a commonly used laser material for solid-state high power, high PRF lasers. Gadolinium scandium gallium garnet doubled doped with neodymium and chromium (Nd:Cr:GSGG) shows higher efficiency than the Nd:YAG laser. The authors previously reported the bulk and surface damage thresholds of the Nd:Cr:GSGG crystal. The surface damage threshold measurements for the Nd:YAG and the Nd:Cr:GSGG are reported in this paper. Infrared absorption spectroscopy was used to analyze surface contaminants. The data show that the organic contaminants, CHn, derived from hydrocarbon (skin oil) associated with improper parts handling, significantly reduce the surface damage threshold

  3. A multi-channel monolithic Ge detector system for fluorescence x-ray absorption spectroscopy

    Construction and performance of a monolithic quad-pixel Ge detector for fluorescence x-ray absorption spectroscopy (XAS) at synchrotron radiation sources are described. The detector semiconductor element has an active surface area of 4.0 cm2 which is electrically separated into four 1.0 cm2 pixels, with little interfacial dead volume. Spatial response of the array shows that cross-talk between adjacent pixels is 55Fe test source (MnKα, 5.9 keV), energy resolution of better than 200 eV is achieved with a 4 μsec peaking time. At 0.5 μsec peaking time, pulse pileup results in a 75% throughput efficiency for an incoming count rate of 100 kHz. Initial XAS fluoresncece measurements at the beamline 4 wiggler end stations at SSRL show that the detector system has several advantages over commercial x-ray spectrometers for low-concentration counting

  4. Study on the surface hydroxyl group on solid breeding materials by infrared absorption spectroscopy

    Tanaka, Satoru; Taniguchi, Masaki [Tokyo Univ. (Japan). Faculty of Engineering

    1996-10-01

    Hydroxyl groups on the surface of Li{sub 2}O were studied by using a diffuse reflectance method with Fourier transform infrared absorption spectroscopy at high temperature up to 973K under controlled D{sub 2}O or D{sub 2} partial pressure. It was found that hydroxyl groups could exist on Li{sub 2}O surface up to 973K under Ar atmosphere. Under D{sub 2}O containing atmosphere, only the sharp peak at 2520cm{sup -1} was observed at 973K in the O-D stretching vibration region. Below 973K, multiple peaks due to the surface -OD were observed and they showed different behavior with temperature or atmosphere. Multiple peaks mean that surface is not homogeneous for D{sub 2}O adsorption. Assignment of the observed peaks to the surface bonding structure was also discussed. (author)

  5. Performance improvements in temperature reconstructions of 2-D tunable diode laser absorption spectroscopy (TDLAS)

    Choi, Doo-Won; Jeon, Min-Gyu; Cho, Gyeong-Rae; Kamimoto, Takahiro; Deguchi, Yoshihiro; Doh, Deog-Hee

    2016-02-01

    Performance improvement was attained in data reconstructions of 2-dimensional tunable diode laser absorption spectroscopy (TDLAS). Multiplicative Algebraic Reconstruction Technique (MART) algorithm was adopted for data reconstruction. The data obtained in an experiment for the measurement of temperature and concentration fields of gas flows were used. The measurement theory is based upon the Beer-Lambert law, and the measurement system consists of a tunable laser, collimators, detectors, and an analyzer. Methane was used as a fuel for combustion with air in the Bunsen-type burner. The data used for the reconstruction are from the optical signals of 8-laser beams passed on a cross-section of the methane flame. The performances of MART algorithm in data reconstruction were validated and compared with those obtained by Algebraic Reconstruction Technique (ART) algorithm.

  6. High resolution electron energy loss spectroscopy: A new probe of subgap absorption in amorphous solids

    The use of high resolution electron energy spectroscopy (HREELS) as a new method for studies of subgap absorption in thin films of amorphous semiconductors is demonstrated. For a-Si films, the α(ω) values extracted from the measured loss spectra are in quantitative agreement with previous optical measurements. The method is also applied to both threefold and diamond-like amorphous carbon films, yielding α(ω) down to considerably lower energies (∼50 meV) than previously reported. The HREELS method is shown to be complementary to existing techniques in that it can access the regime of low energies and ultrathin films which is difficult to investigate with the conventional methods. copyright 1996 American Institute of Physics

  7. Active differential optical absorption spectroscopy for NO2 gas pollution using blue light emitting diodes

    Aljalal, Abdulaziz; Gasmi, Khaled; Al-Basheer, Watheq

    2015-05-01

    Availability of high intensity light emitting diodes in the blue region offer excellent opportunity for using them in active Differential Optical Absorption Spectroscopy (DOAS) to detect air pollution. Their smooth and relatively broad spectral emissions as well as their long life make them almost ideal light sources for active DOAS. In this study, we report the usage of a blue light emitting diode in an active DOAS setup to measure traces of NO2 gas and achieving few parts per billion detection limit for a path length of 300 m. Details of the setup will be presented along with the effects on measurement accuracy due to shifts in the measured spectra calibration and due to using theoretical instrument Gaussian function instead of the measured instrument function.

  8. [Air pollutants study by differential optical absorption spectroscopy with transmit-receive fibers].

    Wei, Yong-Jie; Geng, Xiao-Juan; Chen, Bo; Liu, Cui-Cui; Chen, Wen-Liang

    2013-10-01

    The differential optical absorption spectroscopy system is presented to monitor air pollutants, such as SO2, NO2, etc. The system employs a reflective telescope to collimate light source and focus absorbed light. A combined transmitting and receiving fiber bundle is set to the focus of a concave mirror. A Xenon lamp works as the light source. The light is coupled into the transmitting fiber, and then collimated by the reflective telescope system. After absorbed by the pollutants, the light is reflected by a pyramid mirror far away the telescope. Then the absorbed light is incident on the concave mirror the second time, and focused on the focal plane again. The receiving fiber induces the light which carries the information of the measured gas into a spectrometer. We can get the concentration of the pollutants by DOAS algorithm. Experimental results show that the proposed method can be adopted to measure some pollutants in air quality monitoring. PMID:24409736

  9. Infrared Absorption Spectroscopy and Chemical Kinetics of Free Radicals, Final Technical Report

    Curl, Robert F.; Glass, Graham P.

    2004-11-01

    This research was directed at the detection, monitoring, and study of the chemical kinetic behavior by infrared absorption spectroscopy of small free radical species thought to be important intermediates in combustion. Work on the reaction of OH with acetaldehyde has been completed and published and work on the reaction of O({sup 1}D) with CH{sub 4} has been completed and submitted for publication. In the course of our investigation of branching ratios of the reactions of O({sup 1}D) with acetaldehyde and methane, we discovered that hot atom chemistry effects are not negligible at the gas pressures (13 Torr) initially used. Branching ratios of the reaction of O({sup 1}D) with CH{sub 4} have been measured at a tenfold higher He flow and fivefold higher pressure.

  10. Electronic topological transition in zinc under pressure: An x-ray absorption spectroscopy study

    Zinc metal has been studied at high pressure using x-ray absorption spectroscopy. In order to investigate the role of the different degrees of hydrostaticity on the occurrence of structural anomalies following the electronic topological transition, two pressure transmitting media have been used. Results show that the electronic topological transition, if it exists, does not induce an anomaly in the local environment of compressed Zn as a function of hydrostatic pressure and any anomaly must be related to a loss of hydrostaticity of the pressure transmitting medium. The near-edge structures of the spectra, sensitive to variations in the electronic density of states above the Fermi level, do not show any evidence of electronic transition whatever pressure transmitting medium is used

  11. Dual-laser absorption spectroscopy of C2H2 at 1.4 μ m

    Fasci, E.; Odintsova, T. A.; Castrillo, A.; De Vizia, M. D.; Merlone, A.; Bertiglia, F.; Moretti, L.; Gianfrani, L.

    2016-04-01

    Spectroscopic parameters (line intensity factor, pressure self-broadening, and shifting coefficients) of C2H2 at 1.4 μ m were accurately measured using a dual-laser approach, based upon the technique of optical phase locking. This generated an absolute frequency scale underneath the absorption spectra. A pair of extended-cavity diode lasers was used. One of them, the probe laser, is forced to maintain a precise frequency offset from a reference laser, which is an optical frequency standard based on noise-immune cavity-enhanced optical heterodyne molecular spectroscopy. Laser-gas interaction takes place inside an isothermal multipass cell that is stabilized at the temperature of the triple point of water. The fidelity in the observation of the shape associated to the Pe(14) line of the 2 ν3+ν5 band allowed us to measure the spectroscopic parameters, with a global uncertainty for the line strength of 0.22%.

  12. Natural gas pipeline leak detector based on NIR diode laser absorption spectroscopy

    Gao, Xiaoming; Fan, Hong; Huang, Teng; Wang, Xia; Bao, Jian; Li, Xiaoyun; Huang, Wei; Zhang, Weijun

    2006-09-01

    The paper reports on the development of an integrated natural gas pipeline leak detector based on diode laser absorption spectroscopy. The detector transmits a 1.653 μm DFB diode laser with 10 mW and detects a fraction of the backscatter reflected from the topographic targets. To eliminate the effect of topographic scatter targets, a ratio detection technique was used. Wavelength modulation and harmonic detection were used to improve the detection sensitivity. The experimental detection limit is 50 ppm m, remote detection for a distance up to 20 m away topographic scatter target is demonstrated. Using a known simulative leak pipe, minimum detectable pipe leak flux is less than 10 ml/min.

  13. Molecular electronic states in charge transfer complex studied by x-ray absorption spectroscopy

    The electronic states of tetrathiafulvalene (TTF: TTF = C6H4S4) molecule in organic ferroelectric TTF-p-bromanil (TTF-BA: BA = C6Br4O2) and TTF crystals have been investigated by x-ray absorption spectroscopy (XAS) measurement at S K-edge. We elucidated that the peak structure at 2470.5 eV directly reflects the existence of hole in the highest occupied molecular orbital (HOMO) state of the TTF molecule in TTF-BA; that is consistent with the ionic TTF molecule (TTF+). The XAS of TTF-BA was evaluated on the basis of first-principles calculations, and the calculated spectra reproduce well the shape of experimental spectrum and the peak energy of the HOMO state.

  14. Diffuse-light absorption spectroscopy by fiber optics for detecting and quantifying the adulteration of extra virgin olive oil

    Mignani, A. G.; Ciaccheri, L.; Ottevaere, H.; Thienpont, H.; Conte, L.; Marega, M.; Cichelli, A.; Attilio, C.; Cimato, A.

    2010-09-01

    A fiber optic setup for diffuse-light absorption spectroscopy in the wide 400-1700 nm spectral range is experimented for detecting and quantifying the adulteration of extra virgin olive oil caused by lower-grade olive oils. Absorption measurements provide spectral fingerprints of authentic and adulterated oils. A multivariate processing of spectroscopic data is applied for discriminating the type of adulterant and for predicting its fraction.

  15. Rapid Mapping of Lithiation Dynamics in Transition Metal Oxide Particles with Operando X-ray Absorption Spectroscopy

    Lea Nowack; Daniel Grolimund; Vallerie Samson; Federica Marone; Vanessa Wood

    2016-01-01

    Since the commercialization of lithium ion batteries (LIBs), layered transition metal oxides (LiMO2, where M = Co, Mn, Ni, or mixtures thereof) have been materials of choice for LIB cathodes. During cycling, the transition metals change their oxidation states, an effect that can be tracked by detecting energy shifts in the X-ray absorption near edge structure (XANES) spectrum. X-ray absorption spectroscopy (XAS) can therefore be used to visualize and quantify lithiation kinetics in transition...

  16. Spectral Studies of Ocean Water with Space-borne Sensor SCIAMACHY using Differential Optical Absorption Spectroscopy (DOAS).

    M. Vountas; Dinter, T.; Bracher, A.; Burrows, J.P.; Sierk, B.

    2007-01-01

    Methods enabling the retrieval of oceanic parameter from the space borne instrumentation Scanning Imaging Absorption Spectrometer for Atmospheric ChartographY (SCIAMACHY) using Differential Optical Absorption Spectroscopy (DOAS) are presented. SCIAMACHY onboard ENVISAT measures back scattered solar radiation at a spectral resolution (0.2 to 1.5 nm). The DOAS method was used for the first time to fit modelled Vibrational Raman Scattering (VRS) in...

  17. Study on the Interaction between CdSe Quantum Dots and Bovine Serum Albumin with Ultraviolet Visible Absorption Spectroscopy

    He You HAN; De Hong HU; Jian Gong LIANG; Zong Hai SHENG

    2006-01-01

    The interaction of CdSe quantum dots (QDs) with bovine serum albumin (BSA) has been investigated with ultraviolet visible absorption spectroscopy (UVAS). It was found that the absorption intensity of CdSe QDs significantly decreased after adding BSA solution, showing that CdSe QDs were bonded to BSA. The binding molar ratio was 1:1 and the binding constant was 9.7 × 106 L mol-1.

  18. Application of X-ray absorption spectroscopy and anomalous small angle scattering to RNA polymerase

    X-ray absorption spectroscopy is ideally suited for the investigation of the electronic structure and the local environment (≤∝5 A) of specific atoms in biomolecules. While the edge region provides information about the valence state of the absorbing atom, the chemical identity of neighboring atoms, and the coordination geometry, the EXAFS region contains information about the number and average distance of neighboring atoms and their relative disorder. The development of sensitive detection methods has allowed studies using near-physiological concentrations (as low as ∝100 μM). With careful choice of model compounds, judicious use of fitting procedures, and consideration of the results of biochemical and other spectrOScopic results, this data has provided pivotal information about the structures of these active sites which store energy in their conformation changes or ligand exchanges. Although the application of anomalous small angle scattering to biomolecules has occurred more recently, it clearly provides a method of determining distances between active sites that are outside the range of X-ray absorption spectroscopy. The wavelength dependence of the X-ray scattering power varies rapidly near the edge of the absorbing atom in both amplitude and phase. This behavior selectively alters the contribution of the absorbing atom to the scattering pattern. The structure-function relationship of the intermediate states provide the key to understanding the mechanisms of these complex molecules. It is this precise structural information about the active sites that is not obtainable by other spectroscopic techniques. Combination of these techniques offers a unique approach to the determination of the organization of active sites in biomolecules, especially metalloenzymes. Application of these methods to the substrate and template binding sites of RNA polymerase which contain zinc atoms demonstrates the versatility of this approach. (orig.)

  19. Application of mid-infrared tuneable diode laser absorption spectroscopy to plasma diagnostics: a review

    Within the last decade mid-infrared absorption spectroscopy over a region from 3 to 17μm and based on tuneable lead salt diode lasers, often called tuneable diode laser absorption spectroscopy or TDLAS, has progressed considerably as a powerful diagnostic technique for in situ studies of the fundamental physics and chemistry in molecular plasmas. The increasing interest in processing plasmas containing hydrocarbons, fluorocarbons, organo-silicon and boron compounds has led to further applications of TDLAS because most of these compounds and their decomposition products are infrared active. TDLAS provides a means of determining the absolute concentrations of the ground states of stable and transient molecular species, which is of particular importance for the investigation of reaction kinetic phenomena. Information about gas temperature and population densities can also be derived from TDLAS measurements. A variety of free radicals and molecular ions have been detected by TDLAS. Since plasmas with molecular feed gases are used in many applications such as thin film deposition, semiconductor processing, surface activation and cleaning, and materials and waste treatment, this has stimulated the adaptation of infrared spectroscopic techniques to industrial requirements. The recent development of quantum cascade lasers (QCLs) offers an attractive new option for the monitoring and control of industrial plasma processes. The aim of the present paper is threefold: (i) to review recent achievements in our understanding of molecular phenomena in plasmas (ii) to report on selected studies of the spectroscopic properties and kinetic behaviour of radicals and (iii) to describe the current status of advanced instrumentation for TDLAS in the mid-infrared

  20. Adsorption of mercury on lignin: Combined surface complexation modeling and X-ray absorption spectroscopy studies

    Adsorption of mercury (Hg) on lignin was studied at a range of pH values using a combination of batch adsorption experiments, a surface complexation model (SCM) and synchrotron X-ray absorption spectroscopy (XAS). Surface complexation modeling indicates that three types of acid sites on lignin surfaces, namely aliphatic carboxylic-, aromatic carboxylic- and phenolic-type surface groups, contributed to Hg(II) adsorption. The bond distance and coordination number of Hg(II) adsorption samples at pH 3.0, 4.0 and 5.5 were obtained from extended X-ray absorption fine structure (EXAFS) spectroscopy analysis. The results of SCM and XAS combined reveal that the predominant adsorption species of Hg(II) on lignin changes from HgCl20 to monodentate complex –C–O–HgCl and then bidentate complex –C–O–Hg–O–C– with increasing pH value from 2.0 to 6.0. The good agreement between SCM and XAS results provides new insight into understanding the mechanisms of Hg(II) adsorption on lignin. - Highlights: ► Lignin exhibits a high Hg(II) adsorption capability. ► Adsorption of Hg(II) on lignin is strongly pH-dependent. ► HgCl20, –C–O–HgCl and –C–O–Hg–O–C– are the main adsorption species of Hg(II). - Adsorption of Hg(II) on lignin is strongly pH-dependent, and the main adsorption Hg(II) species change from HgCl20 to –C–O–HgCl and –C–O–Hg–O–C– as pH increases from 2.0 to 6.0.

  1. Optical analysis of trapped Gas—Gas in Scattering Media Absorption Spectroscopy

    Svanberg, S.

    2010-01-01

    An overview of the new field of Gas in Scattering Media Absorption Spectroscopy (GASMAS) is presented. The technique investigates sharp gas spectral signatures, typically 10000 times sharper than those of the host material, in which the gas is trapped in pores or cavities. The presence of pores causes strong multiple scattering. GASMAS combines narrow-band diode-laser spectroscopy, developed for atmospheric gas monitoring, with diffuse media optical propagation, well-known from biomedical optics. Several applications in materials science, food packaging, pharmaceutics and medicine have been demonstrated. So far molecular oxygen and water vapour have been studied around 760 and 935 nm, respectively. Liquid water, an important constituent in many natural materials, such as tissue, has a low absorption at such wavelengths, and this is also true for haemoglobin, making propagation possible in many natural materials. Polystyrene foam, wood, fruits, food-stuffs, pharmaceutical tablets, and human sinus cavities (frontal, maxillary and mastoideal) have been studied, demonstrating new possibilities for characterization and diagnostics. Transport of gas in porous media (diffusion) can be studied by first subjecting the material to, e.g., pure nitrogen, and then observing the rate at which normal, oxygen-containing air, reinvades the material. The conductance of the passages connecting a sinus with the nasal cavity can be objectively assessed by observing the oxygen gas dynamics when flushing the nose with nitrogen. Drying of materials, when liquid water is replaced by air and water vapour, is another example of dynamic processes which can be studied. The technique has also been extended to remote-sensing applications (LIDAR-GASMAS or Multiple-Scattering LIDAR).

  2. Americium characterization by X-ray fluorescence and absorption spectroscopy in plutonium uranium mixed oxide

    Plutonium uranium mixed oxide (MOX) fuels are currently used in nuclear reactors. The actinides in these fuels need to be analyzed after irradiation for assessing their behaviour with regard to their environment and the coolant. In this work the study of the atomic structure and next-neighbour environment of Am in the (Pu,U)O2 lattice in an irradiated (60 MW d kg−1) MOX sample was performed employing micro-X-ray fluorescence (µ-XRF) and micro-X-ray absorption fine structure (µ-XAFS) spectroscopy. The chemical bonds, valences and stoichiometry of Am (∼0.66 wt%) are determined from the experimental data gained for the irradiated fuel material examined in its peripheral zone (rim) of the fuel. In the irradiated sample Am builds up as Am3+ species within an [AmO8]13− coordination environment (e.g. >90%) and no (III XAFS spectra recorded for the irradiated MOX sub-sample in the rim zone for a 300 μm×300 μm beam size area investigated over six scans of 4 h. The records remain constant during multi-scan. The analysis of the XAFS signal shows that Am is found as trivalent in the UO2 matrix. This analytical work shall open the door of very challenging analysis (speciation of fission product and actinides) in irradiated nuclear fuels. - Highlights: • Americium was characterized by microX-ray absorption spectroscopy in irradiated MOX fuel. • The americium redox state as determined from XAS data of irradiated fuel material was Am(III). • In the sample, the Am3+ face an AmO813− coordination environment in the (Pu,U)O2 matrix. • The americium dioxide is reduced by the uranium dioxide matrix

  3. Speciation of copper in a range of food types by X-ray absorption spectroscopy.

    Ceko, Melanie J; Aitken, Jade B; Harris, Hugh H

    2014-12-01

    Copper (Cu) is an essential element and the effects of diets deficient in it are well established. However, the effects of long-term high copper intake are less clear. The chemical form of copper from food sources and its resultant bioavailability is a potentially important factor in its biological activity. X-ray Absorption Near-Edge Structure (XANES) was used to determine the chemical forms of Cu in a range of foods that would make significant contributions to total copper absorption in a standard diet, as well as a chlorinated tap water sample. Analysis of the Cu K-edge XANES spectra suggested that Cu existed in both Cu(I) and Cu(II) forms, with the following five model compounds: Cu(I) acetate; Cu(II) acetate; Cu(I)-glutathione; Cu(I)-cysteine; and, Cu(II)-histidine being fitted to the sample spectra. This research suggested that the absorption of dietary copper could vary markedly dependent on the types of food consumed and the different bioavailability of the Cu species they contain. PMID:24996304

  4. New niobium and rhenium halides synthesis routes by atomic vaporization. X-ray absorption spectroscopy characterization

    New synthetic route as the so called 'chimie douce' or MVS (Metal Vapor Synthesis) has been an increasing field lately to synthesize new kind of solid state structures. Our interest is the assembly of small molecular building blocks of early transition metal halides. We illustrate the use of vaporized rare earth metals to condense NbCls units. We probed the local order around the Nb atom with X-Ray Absorption Spectroscopy, far Infra-Red and XPS in order to better understand the mechanisms involved. A first EXAFS, IR and XPS study on solid state products has shown the evolution of the NbCl5 dimer towards a chain like structure. However, the condensation patterns depends on the rare earth atoms vaporized. These results have been confirmed by X-ray Absorption ab initio calculations. Because our compounds are extremely air sensitive we have developed in situ MVS reactor to take 'snapshots' of the structural intermediates by EXAFS. This study showed the condensation of the initial NbCl5 building blocks by reduction of the Nb oxidation state by rare earth vaporization. This method is a new way of looking at condensation mechanisms via structural evolution observed by EXAFS. (author)

  5. Vacuum-UV absorption spectroscopy of interstellar ice analogues. III. Isotopic effects

    Cruz-Diaz, G A; Chen, Y -J

    2014-01-01

    This paper reports the first measurements of solid-phase vacuum-ultraviolet (VUV) absorption cross-sections of heavy isotopologues present in icy dust grain mantles of dense interstellar clouds and cold circumstellar environments. Pure ices composed of D2O, CD3OD, 13CO2, and 15N15N were deposited at 8 K, a value similar to the coldest dust temperatures in space. The column density of the ice samples was measured in situ by infrared spectroscopy in transmittance. VUV spectra of the ice samples were collected in the 120-160 nm (10.33-7.74 eV) range using a commercial microwave discharged hydrogen flow lamp as the VUV source. Prior to this work, we have recently submitted a similar study of the light isotopologues (Cruz-Diaz, Mu\\~noz Caro and Chen). The VUV spectra are compared to those of the light isotopologues in the solid phase, and to the gas phase spectra of the same molecules. Our study is expected to improve very significantly the models that estimate the VUV absorption of ice mantles in space, which hav...

  6. Electronic absorption spectroscopy probed side-chain movement in chromic transitions of polydiacetylene vesicles.

    Potisatityuenyong, Anupat; Rojanathanes, Rojrit; Tumcharern, Gamolwan; Sukwattanasinitt, Mongkol

    2008-05-01

    Thermochromism, solvatochromism, and alkalinochromism of a poly-10,12-pentacosadiynoic acid (poly(PCDA)) vesicle solution are studied by electronic absorption spectroscopy. The spectroscopic profiles reveal different sequences of side-chain movement during the chromic transitions. The gradual hypsochromic shift and reversibility of the purple solution at low temperature in the thermochromic transition indicates that the transition starts with reversible conformational alteration of methylene side chains leading to metastable purple vesicles. Further heating to 80 degrees C or higher eventually causes the hydrogen bonds at the carboxylic head groups to break and turns the vesicle solution to red. The irreversibility of the red vesicles indicates that it is the most thermodynamically stable form. In the ethanolochromism and alkalinochromism, the processes are however induced at the vesicle-media interface, directly bringing about the hydrogen bond breaking. The purple solutions observed in the ethanolochromism and alkalinochromism cannot reverse back to the blue one. The absorption spectra clearly demonstrate that they are mixtures of the blue and red vesicles. PMID:18366237

  7. In Situ X-Ray Absorption Spectroscopy Study of the LiNiO2 Electrode

    Mansour, A. N.; McBreen, J.; Melendres, C. A.

    1997-03-01

    LiNiO2 is one of the most promising active material for the development of novel 4V rechargeable lithium batteries. Recent x-ray diffraction studies showed that the electrochemical reactivity of this electrode is sensitive to the structure of the starting material as well as the charged products. To further examine this material, we have conducted an x-ray absorption spectroscopy (XAS) study to determine the structure of this electrode as a function of its charge state. Specifically, the x-ray absorption Ni K-edge energy, the pre-edge structure, and local structure parameters such as bond lengths, coordination numbers and disorders were investigated at various states of charge corresponding to Li_(1-x)NiO2 for x values of 0.0, 0.11, 0.23, 0.34, 0.45, 0.82, and 0.99. The charging which proceeds via lithium de-intercalation was conducted using constant current anodization at 0.5 mA in a non aqueous electrolyte consisting of 1M LiPF6 in 1:1:3 propylene ! carbonate, ethylene carbonate and dimethyl carbonate. The XAS results for this electrode will be compared with those of γ-NiOOH and KNiIO_6, the latter being used as a reference for quadrivalent nickel.

  8. High-resolution absorption spectroscopy of the OH 2Pi 3/2 ground state line

    Wiesemeyer, Helmut; Heyminck, Stefan; Karl, Jacobs; Menten, Karl; Neufeld, David; Requena-Torres, Miguel Angel; Stutzki, Jürgen; 10.1051/0004-6361/201218915

    2012-01-01

    The chemical composition of the interstellar medium is determined by gas phase chemistry, assisted by grain surface reactions, and by shock chemistry. The aim of this study is to measure the abundance of the hydroxyl radical (OH) in diffuse spiral arm clouds as a contribution to our understanding of the underlying network of chemical reactions. Owing to their high critical density, the ground states of light hydrides provide a tool to directly estimate column densities by means of absorption spectroscopy against bright background sources. We observed onboard the SOFIA observatory the 2Pi3/2, J = 5/2 3/2 2.5 THz line of ground-state OH in the diffuse clouds of the Carina-Sagittarius spiral arm. OH column densities in the spiral arm clouds along the sightlines to W49N, W51 and G34.26+0.15 were found to be of the order of 10^14 cm^-2, which corresponds to a fractional abundance of 10^-7 to 10^-8, which is comparable to that of H_2O. The absorption spectra of both species have similar velocity components, and the...

  9. Near infrared tunable diode laser absorption spectroscopy for ethylene concentration analysis

    Pan, W. D. D.; Dai, J. M. M.; Zhang, Y. F. F.; Zhang, L.

    2013-01-01

    The absorption spectra of ethylene (C2H4) located at v5+v9 band near 1626nm involve some strong peaks that are suitable for trace gas concentration detection. They are interference free from other abundant molecules that are normally present in the atmosphere. An ethylene analysis system has been developed based on the tunable diode laser absorption spectroscopy. The high resolution transmission of ethylene near 1626nm has been measured by this system under different concentration. The severe overlapping between neighboring spectral lines of ethylene is observed and they cannot be separated with each other easily under atmospheric pressure and room temperature, so a multi-peaks spectrum recognition method is proposed to separate the ethylene spectrum from other interference gas while the ethylene concentration is ultra low. A mixture of high concentration methane, low concentration ethylene with air is used to evaluate the recognition efficiency. The result shows that the ethylene line can be abstract from strong background interference using multi-peaks spectrum recognition method and the accuracy of concentration measurement can reach about 5% comparing with a mass flow meter.

  10. Application of quantum cascade laser absorption spectroscopy to studies of fluorocarbon molecules

    Welzel, S; Roepcke, J [Leibniz Institute for Plasma Science and Technology, Felix-Hausdorff-Str. 2, D-17489 Greifswald (Germany); Stepanov, S; Meichsner, J, E-mail: welzel@inp-greifswald.d [Institute of Physics, Ernst-Moritz-Arndt University, Felix-Hausdorff-Str. 6, D-17489 Greifswald (Germany)

    2009-03-01

    The recent advent of quantum cascade lasers (QCLs) enables room-temperature mid-infrared spectrometer operation which is particularly favourable for industrial process monitoring and control, i.e. the detection of transient and stable molecular species. Conversely, fluorocarbon containing radio-frequency discharges are of special interest for plasma etching and deposition as well as for fundamental studies on gas phase and plasma surface reactions. The application of QCL absorption spectroscopy to such low pressure plasmas is typically hampered by non-linear effects connected with the pulsed mode of the lasers. Nevertheless, adequate calibration can eliminate such effects, especially in the case of complex spectra where single line parameters are not available. In order to facilitate measurements in fluorocarbon plasmas, studies on complex spectra of CF{sub 4} and C{sub 3}F{sub 8} at 7.86{mu}m (1269 - 1275 cm{sup -1}) under low pressure conditions have been performed. The intra-pulse mode, i.e. pulses of up to 300 ns, was applied yielding highly resolved spectral scans of {approx}1 cm{sup -1} coverage. Effective absorption cross sections were determined and their temperature dependence was studied in the relevant range up to 400 K and found to be non-negligible.

  11. NO2 measurements in Hong Kong using LED based long path differential optical absorption spectroscopy

    Chan, K. L.; Pöhler, D.; Kuhlmann, G.; Hartl, A.; Platt, U.; Wenig, M. O.

    2012-05-01

    In this study we present the first long term measurements of atmospheric nitrogen dioxide (NO2) using a LED based Long Path Differential Optical Absorption Spectroscopy (LP-DOAS) instrument. This instrument is measuring continuously in Hong Kong since December 2009, first in a setup with a 550 m absorption path and then with a 3820 m path at about 30 m to 50 m above street level. The instrument is using a high power blue light LED with peak intensity at 450 nm coupled into the telescope using a Y-fibre bundle. The LP-DOAS instrument measures NO2 levels in the Kowloon Tong and Mongkok district of Hong Kong and we compare the measurement results to mixing ratios reported by monitoring stations operated by the Hong Kong Environmental Protection Department in that area. Hourly averages of coinciding measurements are in reasonable agreement (R = 0.74). Furthermore, we used the long-term data set to validate the Ozone Monitoring Instrument (OMI) NO2 data product. Monthly averaged LP-DOAS and OMI measurements correlate well (R = 0.84) when comparing the data for the OMI overpass time. We analyzed weekly patterns in both data sets and found that the LP-DOAS detects a clear weekly cycle with a reduction on weekends during rush hour peaks, whereas OMI is not able to observe this weekly cycle due to its fix overpass time (13:30-14:30 LT - local time).

  12. Damped Lyman-alpha absorption by disk galaxies with large redshifts. III. Intermediate-resolution spectroscopy

    New intermediate-resolution spectroscopy for six members of a sample of 68 moderate- to high-redshift QSOs is presented. Evidence is reported which indicates that seven strong absorption features in the QSO spectra are due to damped Ly-alpha absorption. A standard curve-of-growth analysis on five of the damped systems is performed, and relevant properties are tabulated and discussed. Six of the seven damped Ly-alpha systems have H I column densities of 2 x 10 to the 20th/sq cm or larger, while the remaining system has an H I column density of about 10 to the 20th/sq cm. It is suggested that damped Ly-alpha systems arise when a sight line intercepts a high-redshift protogalaxy disk containing a quiescent cloud component characterized by high column density and low effective velocity dispersion. At the same time, the sight line usually intercepts a broader turbulent component, which is identified as the halo, characterized by much lower column density and higher effective velocity dispersion. 42 refs

  13. Damped Lyman-alpha absorption by disk galaxies with large redshifts. III. Intermediate-resolution spectroscopy

    Turnshek, D.A.; Wolfe, A.M.; Lanzetta, K.M.; Briggs, F.H.; Cohen, R.D. (Space Telescope Science Institute, Baltimore, MD (USA); Multiple Mirror Telescope Observatory, Tucson, AZ (USA); Pittsburgh Univ., PA (USA); California Univ., La Jolla (USA))

    1989-09-01

    New intermediate-resolution spectroscopy for six members of a sample of 68 moderate- to high-redshift QSOs is presented. Evidence is reported which indicates that seven strong absorption features in the QSO spectra are due to damped Ly-alpha absorption. A standard curve-of-growth analysis on five of the damped systems is performed, and relevant properties are tabulated and discussed. Six of the seven damped Ly-alpha systems have H I column densities of 2 x 10 to the 20th/sq cm or larger, while the remaining system has an H I column density of about 10 to the 20th/sq cm. It is suggested that damped Ly-alpha systems arise when a sight line intercepts a high-redshift protogalaxy disk containing a quiescent cloud component characterized by high column density and low effective velocity dispersion. At the same time, the sight line usually intercepts a broader turbulent component, which is identified as the halo, characterized by much lower column density and higher effective velocity dispersion. 42 refs.

  14. Time-resolved x-ray absorption spectroscopy: Watching atoms dance

    The introduction of pump-probe techniques to the field of x-ray absorption spectroscopy (XAS) has allowed the monitoring of both structural and electronic dynamics of disordered systems in the condensed phase with unprecedented accuracy, both in time and in space. We present results on the electronically excited high-spin state structure of an Fe(II) molecular species, [FeII(bpy)3]2+, in aqueous solution, resolving the Fe-N bond distance elongation as 0.2 A. In addition an analysis technique using the reduced χ2 goodness of fit between FEFF EXAFS simulations and the experimental transient absorption signal in energy space has been successfully tested as a function of excited state population and chemical shift, demonstrating its applicability in situations where the fractional excited state population cannot be determined through other measurements. Finally by using a novel ultrafast hard x-ray 'slicing' source the question of how the molecule relaxes after optical excitation has been successfully resolved using femtosecond XANES.

  15. [Study on Differential Optical Absorption Spectroscopy Data Processing Based on Chirp-Z Transformation].

    Zheng, Hai-ming; Li, Guang-jie; Wu, Hao

    2015-06-01

    Differential optical absorption spectroscopy (DOAS) is a commonly used atmospheric pollution monitoring method. Denoising of monitoring spectral data will improve the inversion accuracy. Fourier transform filtering method is effectively capable of filtering out the noise in the spectral data. But the algorithm itself can introduce errors. In this paper, a chirp-z transform method is put forward. By means of the local thinning of Fourier transform spectrum, it can retain the denoising effect of Fourier transform and compensate the error of the algorithm, which will further improve the inversion accuracy. The paper study on the concentration retrieving of SO2 and NO2. The results show that simple division causes bigger error and is not very stable. Chirp-z transform is proved to be more accurate than Fourier transform. Results of the frequency spectrum analysis show that Fourier transform cannot solve the distortion and weakening problems of characteristic absorption spectrum. Chirp-z transform shows ability in fine refactoring of specific frequency spectrum. PMID:26601381

  16. Commissioning and performance of X-ray absorption spectroscopy beamline at the Siam Photon Laboratory

    We report commissioning results and performance of X-ray absorption spectroscopy (XAS) beamline, BL-8, at the Siam Photon Laboratory. BL-8 has been opened for users since the year 2006. It is tunable by a fixed-exit double crystal monochromator equipped with InSb(1 1 1), Si(1 1 1), and Ge(2 2 0) crystals covering photon energy from 1830 to 9000 eV. Thus elemental absorption K-edges of silicon up to copper can be investigated. Other heavier elements may be studied via their L or M edges. The front end is windowless and the beamline is terminated with a Kapton window followed by the XAS station equipped with ionization chambers for transmission-mode measurements. The measured photon flux at sample is approximately 108-1010 photons/s/100 mA for the 1 mmx10 mm beam size. The commissioning XANES spectra of sulfur standards and EXAFS spectra of copper are presented

  17. X-ray absorption spectroscopy and EPR studies of oriented spinach thylakoid preparations

    Andrews, J.C. [Univ. of California, Berkeley, CA (United States). Dept. of Chemistry]|[Lawrence Berkeley Lab., CA (United States). Structural Biology Div.

    1995-08-01

    In this study, oriented Photosystem II (PS II) particles from spinach chloroplasts are studied with electron paramagnetic resonance (EPR) and x-ray absorption spectroscopy (XAS) to determine more details of the structure of the oxygen evolving complex (OEC). The nature of halide binding to Mn is also studied with Cl K-edge and Mn EXAFS (extended x-ray absorption fine structure) of Mn-Cl model compounds, and with Mn EXAFS of oriented PS II in which Br has replaced Cl. Attention is focused on the following: photosynthesis and the oxygen evolving complex; determination of mosaic spread in oriented photosystem II particles from signal II EPR measurement; oriented EXAFS--studies of PS II in the S{sub 2} state; structural changes in PS II as a result of treatment with ammonia: EPR and XAS studies; studies of halide binding to Mn: Cl K-edge and Mn EXAFS of Mn-Cl model compounds and Mn EXAFS of oriented Br-treated photosystem II.

  18. Time-resolved x-ray absorption spectroscopy: Watching atoms dance

    Milne, Chris J; Pham, Van-Thai; Veen, Renske M van der; El Nahhas, Amal; Lima, Frederico; Vithanage, Dimali A; Chergui, Majed [Laboratoire de Spectroscopie Ultrarapide, Ecole Polytechnique Federale de Lausanne (Switzerland); Gawelda, Wojciech [Laser Processing Group, Instituto de Optica, CSIC (Spain); Johnson, Steven L; Beaud, Paul; Ingold, Gerhard; Grolimund, Daniel; Borca, Camelia; Kaiser, Maik; Abela, Rafael [Swiss Light Source, Paul Scherrer Institut (Switzerland); Benfatto, Maurizio [Laboratori Nazionali di Frascati, INFN (Italy); Hauser, Andreas [Departement de Chimie Physique, Universite de Geneve (Switzerland); Bressler, Christian, E-mail: majed.chergui@epfl.c, E-mail: chris.milne@psi.c [European XFEL Project Team, Deutsches Elektronen Synchrotron (Germany)

    2009-11-15

    The introduction of pump-probe techniques to the field of x-ray absorption spectroscopy (XAS) has allowed the monitoring of both structural and electronic dynamics of disordered systems in the condensed phase with unprecedented accuracy, both in time and in space. We present results on the electronically excited high-spin state structure of an Fe(II) molecular species, [Fe{sup II}(bpy){sub 3}]{sup 2+}, in aqueous solution, resolving the Fe-N bond distance elongation as 0.2 A. In addition an analysis technique using the reduced {chi}{sup 2} goodness of fit between FEFF EXAFS simulations and the experimental transient absorption signal in energy space has been successfully tested as a function of excited state population and chemical shift, demonstrating its applicability in situations where the fractional excited state population cannot be determined through other measurements. Finally by using a novel ultrafast hard x-ray 'slicing' source the question of how the molecule relaxes after optical excitation has been successfully resolved using femtosecond XANES.

  19. [Retrieval of NO2 total vertical columns by direct-sun differential optical absorption spectroscopy].

    Wang, Yang; Xie, Pin-hua; Li, Ang; Xu, Jin; Zeng, Yi; Si, Fu-qi; Wu, Feng-cheng

    2012-04-01

    An appropriate reference spectrum is essential for the direct-sun differential optical absorption spectroscopy (DS-DOAS). It depends on the real reference spectrum to retrieve the total vertical column density (VCD). The spectrum detected at the time with minimum sun zenith angle under the relative clear atmospheric condition in the measurement period was conventionally selected as the reference spectrum. Because there is still untracked NO2 absorption structure in the reference spectrum, the VCD retrieved based on the above spectrum is actually relative VCD, which results in larger error. To solve this problem, a new method was investigated. A convolution of extraterrestrial high-precision solar Fraunhofer spectrum and the instrumental function of the spectrometer was computed and chosen as the reference spectrum. The error induced by NO2 absorption structure in the reference spectrum was removed. Then the fitting error of slant column density (SCD) retrieved by this method was analyzed. The correlation between the absolute SCD and the differential slant column density (dSCD) was calculated. The result shows that the error of SCD retrieved by this new method is below 1.6 x 10(16) molecules x cm(-2) on March 7, 2011, while the error generated by the normal method is about 4.25 x 10(16) molecules x cm(-2). The new method decreased more than 62% error. In addition, the results throughout the day were compared to the troposphere VCD from MAX-DOAS and they are in good agreement. It indicates that the new method could effectively reduce the VCD error of the common way. PMID:22715747

  20. Evaluation wavelength range mapping, a tool to optimize the evaluation window in differential absorption spectroscopy

    Vogel, L.; Sihler, H.; Lampel, J.; Wagner, T.; Platt, U.

    2012-04-01

    Optical remote sensing via Differential Optical Absorption Spectroscopy (DOAS) has become a standard technique to assess various trace gases in the atmosphere. Measurement instruments are usually classified into active instruments applying an artificial light source and passive instruments using natural light sources, e.g., scattered or direct sunlight. Platforms range from ground based to satellites and trace gases are studied in all kinds of different environments. Naturally, the evaluation of gathered spectra needs to be tuned to each specific case and trace gas of interest due to the wide range of measurement conditions, atmospheric compositions and instruments used. A well chosen evaluation wavelength range is crucial to the DOAS technique. It should be as large as possible and include the largest differential absorption features of the trace gas of interest in order to maximize sensitivity. However, the differential optical densities of other absorbers should be minimized in order to prevent interferences between different absorption cross sections. Furthermore, instrumental specific features and wavelength dependent radiative transfer effects may have malicious effects and lead to erroneous values. Usually a compromise needs to be found depending on the conditions at hand. Evaluation wavelength range mapping is an easily applied tool to visualize wavelength depending evaluation features of DOAS and to find the optimal retrieval wavelength range. As an example, synthetic spectra are studied which simulate passive DOAS measurements of stratospheric bromine monoxide (BrO) by Zenith-DOAS and Multi-Axis DOAS (MAX-DOAS) measurements of BrO in volcanic plumes. The influence of the I0-effect and the Ring-effect on the respective retrievals are demonstrated. However, due to the general nature of the tool it is applicable to any DOAS measurement and the technique also allows to study any other wavelength dependent influences on retrieved trace gas columns.

  1. [Near-infrared reflectance spectroscopy analytic model established for the IVDMD of Cichorium intybus L].

    Hu, Chao; Bai, Shi-qie; Zhang, Yu; Yan, Jia-jun; You, Ming-hong; Li, Da-xu; Bai, Ling; Zhang Jin

    2014-08-01

    Chicory (Cichorium intybus L.) is a new type of forage grasses of high yield and quality with a great value of popularization and utilization. In vitro dry matter digestibility (IVDMD) is one of the important indicators of the nutritional value of forage evaluation. For the study of establishment of Chicory IVDMD NIRS quantitative analysis model, seventy-two species with different genotypes, different growth stages of 204 chicory samples of aboveground material were collected, and by Fourier transform near-infrared diffuse reflectance spectroscopy, through the use of different regression algorithms, can comparing different spectral ranges and spectral pretreatment methods, eight chicory IVDMD NIRS calibration models were established, and the best calibration model parameters were chosen. Its calibration coefficient of determination (Ri) and external validation coefficient of determination (Rval2) were 0.95317 and 0.90455, calibration standard deviation (RMSEC) and predictive standard deviation (RMSEP) was 1.977 99% and 2.008 82%, and the correlation coefficient (r) between predicted values and chemical values was 0.95108. The results show that using NIRS to determine chicory IVDMD is feasible, and provided a rapid analysis method for the determination IVDMD of chicory. PMID:25508718

  2. Characterising legacy spent nuclear fuel pond materials using microfocus X-ray absorption spectroscopy.

    Bower, W R; Morris, K; Mosselmans, J F W; Thompson, O R; Banford, A W; Law, K; Pattrick, R A D

    2016-11-01

    Analysis of a radioactive, coated concrete core from the decommissioned, spent nuclear fuel cooling pond at the Hunterston-A nuclear site (UK) has provided a unique opportunity to study radionuclides within a real-world system. The core, obtained from a dividing wall and sampled at the fill level of the pond, exhibited radioactivity (dominantly (137)Cs and (90)Sr) heterogeneously distributed across both painted faces. Chemical analysis of the core was undertaken using microfocus spectroscopy at Diamond Light Source, UK. Mapping of Sr across the surface coatings using microfocus X-ray fluorescence (μXRF) combined with X-ray absorption spectroscopy showed that Sr was bound to TiO2 particles in the paint layers, suggesting an association between TiO2 and radiostrontium. Stable Sr and Cs sorption experiments using concrete coupons were also undertaken to assess their interactions with the bulk concrete in case of a breach in the coating layers. μXRF and scanning electron microscopy showed that Sr was immobilized by the cement phases, whilst at the elevated experimental concentrations, Cs was associated with clay minerals in the aggregates. This study provides a crucial insight into poorly understood infrastructural contamination in complex systems and is directly applicable to the UK's nuclear decommissioning efforts. PMID:27262277

  3. Electronic transitions and fermi edge singularity in polar heterostructures studied by absorption and emission spectroscopy

    Pandey, S.; Cavalcoli, D.; Minj, A.; Fraboni, B.; Cavallini, A.; Gamarra, P.; Poisson, M. A.

    2012-12-01

    Optically induced electronic transitions in nitride based polar heterostructures have been investigated by absorption and emission spectroscopy. Surface photovoltage (SPV), photocurrent (PC), and photo luminescence spectroscopy have been applied to high quality InAlN/AlN/GaN structures to study the optical properties of two dimensional electron gas. Energy levels within the two dimensional electron gas (2DEG) well at the interface between the GaN and AlN have been directly observed by SPV and PC. Moreover, a strong enhancement of the photoluminescence intensity due to holes recombining with electrons at the Fermi Energy, known as fermi energy singularity, has been observed. These analyses have been carried out on InAlN/AlN/GaN heterojunctions with the InAlN barrier layer having different In content, a parameter which affects the energy levels within the 2DEG well as well as the optical signal intensity. The measured energy values are in a very good agreement with the ones obtained by Schrödinger-Poisson simulations.

  4. Studies of solvent effects on reaction dynamics using ultrafast transient absorption spectroscopy

    Harris, Don Ahmasi

    Ultrafast transient absorption spectroscopy was used to investigate the solvent dependent reaction dynamics of two prototypical chemical systems: (1) The ring-opening reaction of 1,3-cyclohexadiene, the isolated chromophore in Provitamin D, and (2) The photolysis of various Vitamin B12 cofactors. We investigated the influence of solvent polarity on the ground state conformational relaxation of 1,3,5-cis hexatriene subsequent to the ring opening of 1,3-cyclohexadiene in methanol and 1-propanol solvents. Comparisons to the conformational relaxation in alkane solvents studied earlier demonstrated a surprising influence of solvent polarity on single bond isomerization. Temperature dependent transient absorption measurements were performed on 1,3,5-cis hexatriene in cyclohexane and 1-propanol to determine the effect of solvent polarity on the activation energy barrier for ground state single bond isomerization. These measurements conclude that the polar solvent lowers the energy barrier for single bond isomerization allowing conformational relaxation to proceed faster in alcohol solvents compared to alkane solvents. With no perceived polar transition state for single bond isomerization, this result disagrees with the conventional view of solvation and differentiates the single bond isomerization dynamics of polyenes from alkanes. Transient absorption spectroscopy was also utilized to study the solvent effects in the photolysis of various B12 cofactors in different environments. We investigated the solvent dependent photolysis of adenosylcobalamin, methylcobalamin, and cyanocobalamin in water and ethylene glycol as a function of solvent temperature. In comparing the radical cage escape of adenosylcobalamin and cyanocobalamin, we determined a larger than expected hydrodynamic radii for the diffusing radicals in water compared to ethylene glycol, thus making necessary a revised perspective of solvent interaction with the diffusing radical. In addition, we investigated the

  5. UV/VUV high sensitivity absorption spectroscopy for diagnosing lighting and processing plasmas and for basic data

    High sensitivity absorption spectroscopy involves the use of modern diode and CCD (charge coupled device) detector arrays to observe fractional absorptions of ultraviolet (UV) and vacuum ultraviolet (VUV) radiation as small as 0.00001. Stable arc lamps provide a continuum in some experiments, but experiments at very high spectral resolution or at VUV wavelengths require the greater spectral radiance of a synchrotron. Absolute densities of excited atoms, atomic ions, and molecular radicals are measured in both processing and lighting plasmas. Basic spectroscopic data needed for the analysis of astrophysical observations from the Hubble Space Telescope are measured using absorption of Fe+ in a hollow cathode discharge. copyright 1996 American Institute of Physics

  6. Spectroscopy of 1S0- 3P1 transition of magnesium atom in an external absorption cell

    Bagayev, S. N.; Baraulya, V. I.; Bonert, A. E.; Goncharov, A. N.; Seydaliev, M. R.

    2001-09-01

    The results of saturated absorption spectroscopy of the intercombination 1S0- 3P1 transition of magnesium atoms at 457 nm in an external absorption cell are presented. A laser system based on a Ti:Sa laser with frequency doubling in a LBO nonlinear crystal was used in these experiments. Saturated absorption resonances of magnesium in an external cell at the 1S0- 3P1 transition have been obtained for the first time. Pressure broadening of resonances equal to 12.5±1.5 kHz/mTorr has been measured.

  7. Time-resolved detection of temperature, concentration, and pressure in a shock tube by intracavity absorption spectroscopy

    Fjodorow, Peter; Fikri, Mustapha; Schulz, Christof; Hellmig, Ortwin; Baev, Valery M.

    2016-06-01

    In this paper, we demonstrate the first application of intracavity absorption spectroscopy (ICAS) for monitoring species concentration, total pressure, and temperature in shock-tube experiments. ICAS with a broadband Er3+-doped fiber laser is applied to time-resolved measurements of absorption spectra of shock-heated C2H2. The measurements are performed in a spectral range between 6512 and 6542 cm-1, including many absorption lines of C2H2, with a time resolution of 100 µs and an effective absorption path length of 15 m. Up to 18-times increase of the total pressure and a temperature rise of up to 1200 K have been monitored. Due to the ability of simultaneously recording many absorption lines in a broad spectral range, the presented technique can also be applied to multi-component analysis of transient single-shot processes in reactive gas mixtures in shock tubes, pulse detonation engines, or explosions.

  8. Retrieval interval mapping, a tool to optimize the spectral retrieval range in differential optical absorption spectroscopy

    Vogel, L.; Sihler, H.; Lampel, J.; Wagner, T.; Platt, U.

    2012-06-01

    Remote sensing via differential optical absorption spectroscopy (DOAS) has become a standard technique to identify and quantify trace gases in the atmosphere. The technique is applied in a variety of configurations, commonly classified into active and passive instruments using artificial and natural light sources, respectively. Platforms range from ground based to satellite instruments and trace-gases are studied in all kinds of different environments. Due to the wide range of measurement conditions, atmospheric compositions and instruments used, a specific challenge of a DOAS retrieval is to optimize the parameters for each specific case and particular trace gas of interest. This becomes especially important when measuring close to the detection limit. A well chosen evaluation wavelength range is crucial to the DOAS technique. It should encompass strong absorption bands of the trace gas of interest in order to maximize the sensitivity of the retrieval, while at the same time minimizing absorption structures of other trace gases and thus potential interferences. Also, instrumental limitations and wavelength depending sources of errors (e.g. insufficient corrections for the Ring effect and cross correlations between trace gas cross sections) need to be taken into account. Most often, not all of these requirements can be fulfilled simultaneously and a compromise needs to be found depending on the conditions at hand. Although for many trace gases the overall dependence of common DOAS retrieval on the evaluation wavelength interval is known, a systematic approach to find the optimal retrieval wavelength range and qualitative assessment is missing. Here we present a novel tool to determine the optimal evaluation wavelength range. It is based on mapping retrieved values in the retrieval wavelength space and thus visualize the consequence of different choices of retrieval spectral ranges, e.g. caused by slightly erroneous absorption cross sections, cross correlations and

  9. X-ray absorption spectroscopy and small-angle x-ray scattering studies of metal nanoparticles using synchrotron radiation

    The synchrotron-radiation-based techniques of x-ray absorption spectroscopy and small-angle x-ray scattering are ideally suited to the characterisation of nanoparticles. Their combined application to study the structural and vibrational properties of elemental metal nanoparticles embedded in silica is described here

  10. A Simplified Digestion Protocol for the Analysis of Hg in Fish by Cold Vapor Atomic Absorption Spectroscopy

    Kristian, Kathleen E.; Friedbauer, Scott; Kabashi, Donika; Ferencz, Kristen M.; Barajas, Jennifer C.; O'Brien, Kelly

    2015-01-01

    Analysis of mercury in fish is an interesting problem with the potential to motivate students in chemistry laboratory courses. The recommended method for mercury analysis in fish is cold vapor atomic absorption spectroscopy (CVAAS), which requires homogeneous analyte solutions, typically prepared by acid digestion. Previously published digestion…

  11. Two instruments based on differential optical absorption spectroscopy (DOAS) to measure accurate ammonia concentrations in the atmosphere

    Volten, H.; Bergwerff, J.B.; Haaima, M.; Lolkema, D.E.; Berkhout, A.J.C.; Hoff, G.R.; Potma, C.J.M.; Wichink Kruit, R.J.; Pul, van W.A.J.; Swart, D.P.J.

    2012-01-01

    We present two Differential Optical Absorption Spectroscopy (DOAS) instruments built at RIVM: the RIVM DOAS and the miniDOAS. Both instruments provide virtually interference-free measurements of NH3 concentrations in the atmosphere, since they measure over an open path, without suffering from inlet

  12. Probing the behaviors of gold nanorods in metastatic breast cancer cells based on UV-vis-NIR absorption spectroscopy.

    Weiqi Zhang

    Full Text Available In this work, behaviors of positively-charged AuNRs in a highly metastatic tumor cell line MDA-MB-231 are examined based on UV-vis-NIR absorption spectroscopy in combination with inductively coupled plasma mass spectrometry (ICP-MS, transmission electron microscopy (TEM and dark-field microscopic observation. It is found that characteristic surface plasmon resonance (SPR peaks of AuNRs can be detected using spectroscopic method within living cells that have taken up AuNRs. The peak area of transverse SPR band is shown to be proportionally related to the amount of AuNRs in the cells determined with ICP-MS, which suggests a facile and real time quantification method for AuNRs in living cells. The shape of longitudinal SPR band in UV-vis-NIR spectrum reflects the aggregation state of AuNRs in the cells during the incubation period, which is proved by TEM and microscopic observations. Experimental results reveal that AuNRs are internalized by the cells rapidly; the accumulation, distribution and aggregation of AuNRs in the cells compartments are time and dose dependent. The established spectroscopic analysis method can not only monitor the behaviors of AuNRs in living cells but may also be helpful in choosing the optimum laser stimulation wavelength for anti-tumor thermotherapy.

  13. Investigation of band gap narrowing in nitrogen-doped La2Ti2O7 with transient absorption spectroscopy.

    Yost, Brandon T; Cushing, Scott K; Meng, Fanke; Bright, Joeseph; Bas, Derek A; Wu, Nianqiang; Bristow, Alan D

    2015-12-14

    Doping a semiconductor can extend the light absorption range, however, it usually introduces mid-gap states, reducing the charge carrier lifetime. This report shows that doping lanthanum dititinate (La2Ti2O7) with nitrogen extends the valence band edge by creating a continuum of dopant states, increasing the light absorption edge from 380 nm to 550 nm without adding mid-gap states. The dopant states are experimentally resolved in the excited state by correlating transient absorption spectroscopy with a supercontinuum probe and DFT prediction. The lack of mid-gap states is further confirmed by measuring the excited state lifetimes, which reveal the shifted band edge only increased carrier thermalization rates to the band edge and not interband charge recombination under both ultraviolet and visible excitation. Terahertz (time-domain) spectroscopy also reveals that the conduction mechanism remains unchanged after doping, suggesting the states are delocalized. PMID:26531849

  14. X-ray absorption spectroscopy in biological systems. Opportunities and limitations

    X-ray absorption spectroscopy has become more important for applications in the material sciences, geology, environmental science and biology, specifically in the field of molecular biology. The scope of this thesis is to add more experimental evidence in order to show how applicable X-ray absorption near edge structure (XANES) is to biology. Two biological systems were investigated, at the molecular level, lead uptake in plants and the effect of silver on bacteria. This investigation also included an analysis of the sensitivity of Pb L3- and Ag L3-XANES spectra with regard to their chemical environment. It was shown that Pb L3- and Ag L3-XANES spectra are sensitive to an environment with at least differences in the second coordination shell. The non-destructive and element specific properties of XANES are the key advantages that were very important for this investigation. However, in both projects the adequate selection of reference compounds, which required in some cases a chemical synthesis, was the critical factor to determine the chemical speciation and, finally, possible uptake and storage mechanisms for plants and antibacterial mechanisms of silver. The chemical environment of Pb in roots and leaves of plants from four different plant families and a lichen from a former lead mining site in the Eifel mountains in Germany was determined using both solid compounds and aqueous solutions of different ionic strength, which simulate the plant environment. The results can be interpreted in such a way that lead is sorbed on the surface of cell walls. Silver bonding as reaction with Staphylococcus aureus, Listeria monocytogenes, and Escherichia coli bacteria was determined using inorganic silver compounds and synthesized silver amino acids. Silver binds to sulfur, amine and carboxyl groups in amino acids.

  15. X-ray absorption spectroscopy in biological systems. Opportunities and limitations

    Bovenkamp, Gudrun Lisa

    2013-05-15

    X-ray absorption spectroscopy has become more important for applications in the material sciences, geology, environmental science and biology, specifically in the field of molecular biology. The scope of this thesis is to add more experimental evidence in order to show how applicable X-ray absorption near edge structure (XANES) is to biology. Two biological systems were investigated, at the molecular level, lead uptake in plants and the effect of silver on bacteria. This investigation also included an analysis of the sensitivity of Pb L{sub 3}- and Ag L{sub 3}-XANES spectra with regard to their chemical environment. It was shown that Pb L{sub 3}- and Ag L{sub 3}-XANES spectra are sensitive to an environment with at least differences in the second coordination shell. The non-destructive and element specific properties of XANES are the key advantages that were very important for this investigation. However, in both projects the adequate selection of reference compounds, which required in some cases a chemical synthesis, was the critical factor to determine the chemical speciation and, finally, possible uptake and storage mechanisms for plants and antibacterial mechanisms of silver. The chemical environment of Pb in roots and leaves of plants from four different plant families and a lichen from a former lead mining site in the Eifel mountains in Germany was determined using both solid compounds and aqueous solutions of different ionic strength, which simulate the plant environment. The results can be interpreted in such a way that lead is sorbed on the surface of cell walls. Silver bonding as reaction with Staphylococcus aureus, Listeria monocytogenes, and Escherichia coli bacteria was determined using inorganic silver compounds and synthesized silver amino acids. Silver binds to sulfur, amine and carboxyl groups in amino acids.

  16. Characterization and speciation of mercury-bearing mine wastes using X-ray absorption spectroscopy

    Kim, C.S.; Brown, Gordon E., Jr.; Rytuba, J.J.

    2000-01-01

    Mining of mercury deposits located in the California Coast Range has resulted in the release of mercury to the local environment and water supplies. The solubility, transport, and potential bioavailability of mercury are controlled by its chemical speciation, which can be directly determined for samples with total mercury concentrations greater than 100 mg kg-1 (ppm) using X-ray absorption spectroscopy (XAS). This technique has the additional benefits of being non-destructive to the sample, element-specific, relatively sensitive at low concentrations, and requiring minimal sample preparation. In this study, Hg L(III)-edge extended X-ray absorption fine structure (EXAFS) spectra were collected for several mercury mine tailings (calcines) in the California Coast Range. Total mercury concentrations of samples analyzed ranged from 230 to 1060 ppm. Speciation data (mercury phases present and relative abundances) were obtained by comparing the spectra from heterogeneous, roasted (calcined) mine tailings samples with a spectral database of mercury minerals and sorbed mercury complexes. Speciation analyses were also conducted on known mixtures of pure mercury minerals in order to assess the quantitative accuracy of the technique. While some calcine samples were found to consist exclusively of mercuric sulfide, others contain additional, more soluble mercury phases, indicating a greater potential for the release of mercury into solution. Also, a correlation was observed between samples from hot-spring mercury deposits, in which chloride levels are elevated, and the presence of mercury-chloride species as detected by the speciation analysis. The speciation results demonstrate the ability of XAS to identify multiple mercury phases in a heterogeneous sample, with a quantitative accuracy of ??25% for the mercury-containing phases considered. Use of this technique, in conjunction with standard microanalytical techniques such as X-ray diffraction and electron probe microanalysis

  17. Ultrafast Excited State Relaxation of a Metalloporphyrin Revealed by Femtosecond X-ray Absorption Spectroscopy.

    Shelby, Megan L; Lestrange, Patrick J; Jackson, Nicholas E; Haldrup, Kristoffer; Mara, Michael W; Stickrath, Andrew B; Zhu, Diling; Lemke, Henrik T; Chollet, Matthieu; Hoffman, Brian M; Li, Xiaosong; Chen, Lin X

    2016-07-20

    Photoexcited Nickel(II) tetramesitylporphyrin (NiTMP), like many open-shell metalloporphyrins, relaxes rapidly through multiple electronic states following an initial porphyrin-based excitation, some involving metal centered electronic configuration changes that could be harnessed catalytically before excited state relaxation. While a NiTMP excited state present at 100 ps was previously identified by X-ray transient absorption (XTA) spectroscopy at a synchrotron source as a relaxed (d,d) state, the lowest energy excited state (J. Am. Chem. Soc., 2007, 129, 9616 and Chem. Sci., 2010, 1, 642), structural dynamics before thermalization were not resolved due to the ∼100 ps duration of the available X-ray probe pulse. Using the femtosecond (fs) X-ray pulses of the Linac Coherent Light Source (LCLS), the Ni center electronic configuration from the initial excited state to the relaxed (d,d) state has been obtained via ultrafast Ni K-edge XANES (X-ray absorption near edge structure) on a time scale from hundreds of femtoseconds to 100 ps. This enabled the identification of a short-lived Ni(I) species aided by time-dependent density functional theory (TDDFT) methods. Computed electronic and nuclear structure for critical excited electronic states in the relaxation pathway characterize the dependence of the complex's geometry on the electron occupation of the 3d orbitals. Calculated XANES transitions for these excited states assign a short-lived transient signal to the spectroscopic signature of the Ni(I) species, resulting from intramolecular charge transfer on a time scale that has eluded previous synchrotron studies. These combined results enable us to examine the excited state structural dynamics of NiTMP prior to thermal relaxation and to capture intermediates of potential photocatalytic significance. PMID:27286410

  18. [Study on determination of plume velocity by passive differential optical absorption spectroscopy].

    Li, Ang; Xie, Pin-hua; Liu, Wen-qing; Liu, Jian-guo; Dou, Ke; Lin, Yi-hui

    2008-10-01

    Differential optical absorption spectroscopy (DOAS) technique has been used to measure various trace gases in the atmosphere by their strongly structured absorption of radiation in the UV and visible spectral range. Passive DOAS using the zenith scattered sunlight as the light source can obtain the continuous column density distribution of air pollutants (such as SO2 and NO2) by scanning the plume emitted from sources on a mobile platform, then with the plume velocity information the total emission value can be ultimately estimated. In practice it is hard to calculate the total emission because there is no efficient way to accurately get the plume velocity which is the most important parameter. Usually the wind speed near ground is used as the actual plume speed, which constitutes the greatest source of uncertainty in the passive DOAS measurements for the total emission calculation. A passive DOAS method for the determination of plume velocity of pollution source was studied in the present paper. Two passive DOAS systems were placed under the plume along the plume transmission direction to observed the scattered sunlight at one fixed sepasation angle, and then the plume velocity was derived from the time delay resulting from the plume moving a certain distance, and also the plume height needed in the plume velocity calculation was measured by the same two passive DOAS systems. Measurement of the plume emitted from a certain power plant was carried out by the two passive DOAS systems and the plume velocities of 3.6 and 5.4 m x s(-1) at two separate moments were derived. The comparison with the wind speed measured at the same time by the single theodolite wind observation method indicates that this optical remote sensing method based on passive DOAS can be used to determine the plume velocity by monitoring the total emission from sources. PMID:19123375

  19. Time-resolved pump-probe X-ray absorption fine structure spectroscopy of Gaq3

    Gallium(tris-8-hydroxyquinoline) (Gaq3) belongs to a class of metal organic compounds, used as electron transport layer and emissive layer in organic light emitting diodes. Many research activities have concentrated on the optical and electronic properties, especially of the homologue molecule aluminum(tris-8-hydroxyquinoline) (Alq3). Knowledge of the first excited state S1 structure of these molecules could provide deeper insight into the processes involved into the operation of electronic devices, such as OLEDs and, hence, it could further improve their efficiency and optical properties. Until now the excited state structure could not be determined experimentally. Most of the information about this structure mainly arises from theoretical calculations. X-ray absorption fine structure (XAFS) spectroscopy is a well developed technique to determine both, the electronic and the geometric properties of a sample. The connection of ultrashort pulsed X-ray sources with a pulsed laser system offers the possibility to use XAFS as a tool for studying the transient changes of a sample induced by a laser pulse. In the framework of this thesis a new setup for time-resolved pump-probe X-ray absorption spectroscopy at PETRA III beamline P11 was developed for measuring samples in liquid form. In this setup the sample is pumped into its photo-excited state by a femtosecond laser pump pulse with 343 nm wavelength and after a certain time delay probed by an X-ray probe pulse. In this way the first excited singlet state S1 of Gaq3 dissolved in benzyl alcohol was analyzed. A structural model for the excited state structure of the Gaq3 molecule based on the several times reproduced results of the XAFS experiments is proposed. According to this model it was found that the Ga-NA bond length is elongated, while the Ga-OA bond length is shortened upon photoexcitation. The dynamics of the structural changes were not the focus of this thesis. Nevertheless the excited state lifetime of Gaq3

  20. X-ray absorption spectroscopy for element selective investigations of structure, valence and magnetism in doped oxides

    Full text: The use of x-ray absorption spectroscopy (XAS) and in particular x-ray linear dichroism (XLD) and x-ray magnetic circular dichroism (XMCD) offers the possibility to study a range of physical properties with element specificity. The combination of XAS at the near edge (XANES) and XLD allows to separately determine the valence state and the local structural environment of dopant atoms, cationic and anionic sublattice in doped oxides. This approach was used for epitaxial films of Co-doped ZnO, Co/Al-codoped ZnO, Co/N-codoped ZnO, Gd-doped ZnO, and Fe/N-codoped TiO2 to determine the incorporation of the respective dopant atoms into the host lattice, its valence state, and at the same time assure phase pureness of the material, when the XANES and XLD measurements are combined with respective simulations. Especially for the Co-doped ZnO system a comprehensive set of quality indicators based on XAS could be established which assure that Co substitutes for Zn and the formation of metallic Co precipitations can be ruled out. In addition, XMCD allows to study the sublattice magnetization of the dopant which can be compared to integral SQUID magnetometry and by that establishing, that e.g. Co-doped ZnO is an anisotropic paramagnet. Signs of ferromagnetic order could be directly attributed to the presence of metallic Co precipitations which could be evidenced by a combination of XANES and transmission electron microscopy. Recently, unprecedented high field XMCD measurements up to 17 Tesla have allowed to quantify the next cation neighbor exchange interaction which has been shown to be antiferromagnetic as inferred before. Here the concept of the comprehensive XAS-based approach will be reviewed to illustrate how XANES allows to determine the valence, XLD the local structure and XMCD the magnetic properties of dopant atoms and host material separately. (author)

  1. Establishment of the correlation law between electron density, infrared absorption and doping concentration in Ga3+-doped ZnO

    Highlights: ► Synthesis of nanometric A3+-doped ZnO by polyol-mediated route. ► Correlation between free electron density and the doping rate of A3+-doped ZnO. ► Optimization of infrared absorbing properties of A3+-doped ZnO. - Abstract: A polyol-mediated synthesis allows the obtaining of doped zinc oxides nanoparticles with tunable infrared absorption properties via the doping concentration. In a first step the prepared nanoparticles are characterized in terms of chemical composition (purity and homogeneity), crystallite size and agglomerate morphology. A correlation law between the infrared absorbing efficiency, the free electron density and the doping concentration is then clearly established; this law is based on the neighboring probability of the dopant ions in the crystal network

  2. On time resolved gas temperature measurements in a pulsed dc plasma using quantum cascade laser absorption spectroscopy

    With a time resolution of 33 µs, the gas temperature in a pulsed dc air plasma admixed with 0.8% NO has been measured by quantum cascade laser absorption spectroscopy (QCLAS). For this purpose, the temperature dependent intensity ratios of two absorption structures of NO at 1900 cm−1 (5.26 µm) have been used. The QCLAS system worked in the Intra Pulse Mode with a pulse repetition frequency of 30 kHz leading to a spectrum recorded each 33 µs. In a low pressure discharge, the influence of nonlinear absorption phenomena causing strong distorted absorption structures of NO has been taken into account by a calibration routine based on tabulated line strengths. Different mean plasma currents have been applied to the discharge leading to gas temperature values ranging from about 300 K up to about 500 K. (paper)

  3. Concentration measurement of NO using self-absorption spectroscopy of the γ band system in a pulsed corona discharge.

    Zhai, Xiaodong; Ding, Yanjun; Peng, Zhimin; Luo, Rui

    2012-07-10

    Nitric oxide (NO) concentrations were measured using the γ band system spectrum based on the strong self-absorption effect of NO in pulsed corona discharges. The radiative transitional intensities of the NO γ band were simulated based on the theory of molecular spectroscopy. The intensities of some bands, especially γ(0,0) and γ(1,0), are weakened by the self-absorption. The correlations between the spectral self-absorption intensities and NO concentration were validated using a modified Beer-Lambert law with a combined factor K relating the branching ratio and the NO concentration, and a nonlinear index α that is applicable to the broadband system. Optical emissive spectra in pulsed corona discharges in NO and N2/He mixtures were used to evaluate the two parameters for various conditions. Good agreement between the experimental and theoretical results verifies the self-absorption behavior seen in the UV spectra of the NO γ bands. PMID:22781235

  4. Identification of lead chemical form in mine waste materials by X-ray absorption spectroscopy

    X-ray absorption spectroscopy (XAS) provides a direct means for measuring lead chemical forms in complex samples. In this study, XAS was used to identify the presence of plumbojarosite (PbFe6(SO4)4(OH)12) by lead L3-edge XANES spectra in mine waste from a small gold mining operation in Fiji. The presence of plumbojarosite in tailings was confirmed by XRD but XANES gave better resolution. The potential for human uptake of Pb from tailings was measured using a physiologically based extract test (PBET), an in-vitro bioaccessibility (BAc) method. The BAc of Pb was 55%. Particle size distribution of tailings indicated that 40% of PM10 particulates exist which could be a potential risk for respiratory effects via the inhalation route. Food items collected in the proximity of the mine site had lead concentrations which exceed food standard guidelines. Lead within the mining lease exceeded sediment guidelines. The results from this study are used to investigate exposure pathways via ingestion and inhalation for potential risk exposure pathways of Pb in that locality. The highest Pb concentration in soil and tailings was 25,839 mg/kg, exceeding the Australian National Environment Protection Measure (NEPM) soil health investigation levels.

  5. X-ray absorption spectroscopy study of a copper-containing material after thermal treatment

    Thermal immobilization of copper contaminant in a copper-containing solid material collected from local copper smelting and foundry area is investigated in the present work. X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD) are employed for copper speciation. XAS results indicate that cupric hydroxide is the major copper species in the solid material dried at 105 deg. C. After being subjected to a 500 deg. C thermal process, cupric hydroxide still remains as the main copper species, but some Cu(II) is chemically reduced to Cu(I). More cupric hydroxide is progressively converted to Cu(I) as the sample was heated at 1100 deg. C than that heated at 500 deg. C. The sample heated at 500 deg. C is in its original powder form. However, thermal treatment at 1100 deg. C transforms the powder into a hardened granule-like form that is much bigger in size and difficult to be ground into powders. The sample is sintered with the sparingly soluble cuprous oxide and elemental copper being encapsulated inside. Toxicity characteristic leaching procedure (TCLP) results depict that amount of copper leached from the sample (containing 133,000 mg copper kg-1) heated at 1100 deg. C for 2 h is considerably minor, being 367 mg copper kg-1

  6. The Chemistry of Spent Nuclear Fuel From X-Ray Absorption Spectroscopy

    Present and future nuclear fuel cycles will require an understanding of the complex chemistry of trace fission products and transuranium actinides in spent nuclear fuel (SNF). Because of the unique analytical challenges presented by SNF to the materials scientist, many of its fundamental physical and chemical properties remain poorly understood, especially on the microscopic scale. Such an understanding of the chemical states of radionuclides in SNF would benefit development of technologies for fuel monitoring, fuel performance improvement and modeling, fuel reprocessing, and spent fuel storage and disposal. We have recently demonstrated the use of synchrotron x-ray absorption spectroscopy (XAS) to examine crystal chemical properties of actinides and fission products in extracted specimens of SNF. Information obtained includes oxidation state, chemical bond coordination, and quantitative elemental concentration and distribution. We have also used XAS in a scanning mode to obtain x-ray spectral micrographs with resolution approaching 1 micron. A brief overview of the technique will be presented, along with findings on uranium, plutonium, neptunium, technetium, and molybdenum in commercial PWR SNF specimens

  7. Serial Femtosecond Crystallography and Ultrafast Absorption Spectroscopy of the Photoswitchable Fluorescent Protein IrisFP.

    Colletier, Jacques-Philippe; Sliwa, Michel; Gallat, François-Xavier; Sugahara, Michihiro; Guillon, Virginia; Schirò, Giorgio; Coquelle, Nicolas; Woodhouse, Joyce; Roux, Laure; Gotthard, Guillaume; Royant, Antoine; Uriarte, Lucas Martinez; Ruckebusch, Cyril; Joti, Yasumasa; Byrdin, Martin; Mizohata, Eiichi; Nango, Eriko; Tanaka, Tomoyuki; Tono, Kensuke; Yabashi, Makina; Adam, Virgile; Cammarata, Marco; Schlichting, Ilme; Bourgeois, Dominique; Weik, Martin

    2016-03-01

    Reversibly photoswitchable fluorescent proteins find growing applications in cell biology, yet mechanistic details, in particular on the ultrafast photochemical time scale, remain unknown. We employed time-resolved pump-probe absorption spectroscopy on the reversibly photoswitchable fluorescent protein IrisFP in solution to study photoswitching from the nonfluorescent (off) to the fluorescent (on) state. Evidence is provided for the existence of several intermediate states on the pico- and microsecond time scales that are attributed to chromophore isomerization and proton transfer, respectively. Kinetic modeling favors a sequential mechanism with the existence of two excited state intermediates with lifetimes of 2 and 15 ps, the second of which controls the photoswitching quantum yield. In order to support that IrisFP is suited for time-resolved experiments aiming at a structural characterization of these ps intermediates, we used serial femtosecond crystallography at an X-ray free electron laser and solved the structure of IrisFP in its on state. Sample consumption was minimized by embedding crystals in mineral grease, in which they remain photoswitchable. Our spectroscopic and structural results pave the way for time-resolved serial femtosecond crystallography aiming at characterizing the structure of ultrafast intermediates in reversibly photoswitchable fluorescent proteins. PMID:26866390

  8. Fabry-Perot Absorption Line Spectroscopy of the Galactic Bar. I. Kinematics

    Rangwala, Naseem; Stanek, K Z

    2008-01-01

    We use Fabry-Perot absorption line imaging spectroscopy to measure radial velocities using the Ca II 8542 line in 3360 stars towards three lines of sight in the Milky Way's bar: Baade's Window and offset position at (l,b) ~ (+-5.0, -3.5). This sample includes 2488 bar red clump giants, 339 bar M/K-giants, and 318 disk main sequence stars. We measure the first four moments of the stellar velocity distribution of the red clump giants, and find it to be symmetric and flat-topped. We also measure the line-of-sight average velocity and dispersion of the red clump giants as a function of distance in the bar. We detect stellar streams at the near and far side of the bar with velocity difference > 30 km/s at l = +-5, but we do not detect two separate streams in Baade's Window. Our M-giants kinematics agree well with previous studies, but have dispersions systematically lower than those of the red clump giants by ~ 10 km/s. For the disk main sequence stars we measure a velocity dispersion of ~ 45 km/s for all three li...

  9. Communication: Hydrogen bonding interactions in water-alcohol mixtures from X-ray absorption spectroscopy.

    Lam, Royce K; Smith, Jacob W; Saykally, Richard J

    2016-05-21

    While methanol and ethanol are macroscopically miscible with water, their mixtures exhibit negative excess entropies of mixing. Despite considerable effort in both experiment and theory, there remains significant disagreement regarding the origin of this effect. Different models for the liquid mixture structure have been proposed to address this behavior, including the enhancement of the water hydrogen bonding network around the alcohol hydrophobic groups and microscopic immiscibility or clustering. We have investigated mixtures of methanol, ethanol, and isopropanol with water by liquid microjet X-ray absorption spectroscopy on the oxygen K-edge, an atom-specific probe providing details of both inter- and intra-molecular structure. The measured spectra evidence a significant enhancement of hydrogen bonding originating from the methanol and ethanol hydroxyl groups upon the addition of water. These additional hydrogen bonding interactions would strengthen the liquid-liquid interactions, resulting in additional ordering in the liquid structures and leading to a reduction in entropy and a negative enthalpy of mixing, consistent with existing thermodynamic data. In contrast, the spectra of the isopropanol-water mixtures exhibit an increase in the number of broken alcohol hydrogen bonds for mixtures containing up to 0.5 water mole fraction, an observation consistent with existing enthalpy of mixing data, suggesting that the measured negative excess entropy is a result of clustering or micro-immiscibility. PMID:27208929

  10. Properties of aqueous nitrate and nitrite from x-ray absorption spectroscopy

    Nitrate and nitrite ions are of considerable interest, both for their widespread use in commercial and research contexts and because of their central role in the global nitrogen cycle. The chemistry of atmospheric aerosols, wherein nitrate is abundant, has been found to depend on the interfacial behavior of ionic species. The interfacial behavior of ions is determined largely by their hydration properties; consequently, the study of the hydration and interfacial behavior of nitrate and nitrite comprises a significant field of study. In this work, we describe the study of aqueous solutions of sodium nitrate and nitrite via X-ray absorption spectroscopy (XAS), interpreted in light of first-principles density functional theory electronic structure calculations. Experimental and calculated spectra of the nitrogen K-edge XA spectra of bulk solutions exhibit a large 3.7 eV shift between the XA spectra of nitrate and nitrite resulting from greater stabilization of the nitrogen 1s energy level in nitrate. A similar shift is not observed in the oxygen K-edge XA spectra of NO3− and NO2−. The hydration properties of nitrate and nitrite are found to be similar, with both anions exhibiting a similar propensity towards ion pairing

  11. Assessment of the performance of a compact concentric spectrometer system for Atmospheric Differential Optical Absorption Spectroscopy

    Whyte, C.; Leigh, R. J.; Lobb, D.; Williams, T.; Remedios, J. J.; Cutter, M.; Monks, P. S.

    2009-12-01

    A breadboard demonstrator of a novel UV/VIS grating spectrometer has been developed based upon a concentric arrangement of a spherical meniscus lens, concave spherical mirror and curved diffraction grating suitable for a range of atmospheric remote sensing applications from the ground or space. The spectrometer is compact and provides high optical efficiency and performance benefits over traditional instruments. The concentric design is capable of handling high relative apertures, owing to spherical aberration and comma being near zero at all surfaces. The design also provides correction for transverse chromatic aberration and distortion, in addition to correcting for the distortion called "smile", the curvature of the slit image formed at each wavelength. These properties render this design capable of superior spectral and spatial performance with size and weight budgets significantly lower than standard configurations. This form of spectrometer design offers the potential for exceptionally compact instrument for differential optical absorption spectroscopy (DOAS) applications from LEO, GEO, HAP or ground-based platforms. The breadboard demonstrator has been shown to offer high throughput and a stable Gaussian line shape with a spectral range from 300 to 450 nm at 0.5 nm resolution, suitable for a number of typical DOAS applications.

  12. Interaction of ester functional groups with aluminum oxide surfaces studied using infrared reflection absorption spectroscopy.

    van den Brand, J; Blajiev, O; Beentjes, P C J; Terryn, H; de Wit, J H W

    2004-07-20

    The bonding of two types of ester group-containing molecules with a set of different oxide layers on aluminum has been investigated using infrared reflection absorption spectroscopy. The different oxide layers were made by giving typical surface treatments to the aluminum substrate. The purpose of the investigation was to find out what type of ester-oxide bond is formed and whether this is influenced by changes in the composition and chemistry of the oxide. The extent by which these bonded ester molecules resisted disbondment in water or substitution by molecules capable of chemisorption was also investigated. The ester groups were found to show hydrogen bonding with hydroxyls on the oxide surfaces through their carbonyl oxygens. For all oxides, the ester groups showed the same nu(C = O) carbonyl stretching vibration after adsorption, indicating very similar bonding occurs. However, the oxides showed differences in the amount of molecules bonded to the oxide surface, and a clear relation was observed with the hydroxyl concentration present on the oxide surface, which was determined from XPS measurements. The two compounds showed differences in the free to bonded nu(C = O) infrared peak shift, indicating differences in bonding strength with the oxide surface between the two types of molecules. The bonding of the ester groups with the oxide surfaces was found to be not stable in the presence of water and also not in the presence of a compound capable of chemisorption with the aluminum oxide surface. PMID:15248718

  13. Determination of uranyl incorporation into biogenic manganese oxides using X-ray absorption spectroscopy and scattering

    Webb, S.M.; Fuller, C.C.; Tebo, B.M.; Bargar, J.R.

    2006-01-01

    Biogenic manganese oxides are common and an important source of reactive mineral surfaces in the environment that may be potentially enhanced in bioremediation cases to improve natural attenuation. Experiments were performed in which the uranyl ion, UO22+ (U(VI)), at various concentrations was present during manganese oxide biogenesis. At all concentrations, there was strong uptake of U onto the oxides. Synchrotron-based extended X-ray absorption fine structure (EXAFS) spectroscopy and X-ray diffraction (XRD) studies were carried out to determine the molecular-scale mechanism by which uranyl is incorporated into the oxide and how this incorporation affects the resulting manganese oxide structure and mineralogy. The EXAFS experiments show that at low concentrations (2 mol % U, >4 ??M U(VI) in solution), the presence of U(VI) affects the stability and structure of the Mn oxide to form poorly ordered Mn oxide tunnel structures, similar to todorokite. EXAFS modeling shows that uranyl is present in these oxides predominantly in the tunnels of the Mn oxide structure in a tridentate complex. Observations by XRD corroborate these results. Structural incorporation may lead to more stable U(VI) sequestration that may be suitable for remediation uses. These observations, combined with the very high uptake capacity of the Mn oxides, imply that Mn-oxidizing bacteria may significantly influence dissolved U(VI) concentrations in impacted waters via sorption and incorporation into Mn oxide biominerals. ?? 2006 American Chemical Society.

  14. ''Live'' Prussian blue fading by time-resolved X-ray absorption spectroscopy

    Prussian blue (PB) is an artists' pigment that has been frequently used in many artworks but poses several problems of conservation because of its fading under light and anoxia treatment. PB fading is due to the reduction of iron(III) into iron(II) and depends a lot on the object investigated. Due to the complexity of the structure, the precise physico-chemical mechanisms behind the redox process remain obscure. In this paper, we present a procedure to investigate light- and anoxia-induced fading of PB-paper samples by means of time resolved X-ray absorption spectroscopy performed at the Fe K-edge. A system composed of a visible light source and a flux-controlled environmental cell allowed light, gas and humidity to be modified in situ. The synchrotron X-ray beam was evidenced to induce a reduction of PB and to play a major role in the kinetics. The analysis of the PB fading kinetics of a sample submitted to various gas and light environments showed that both synchrotron beam and anoxia were influencing PB reduction in a correlated way. In comparison, light was found to play a minor role. Finally, we have demonstrated that the type of paper substrate could influence significantly the kinetics of reduction. Several hypotheses to explain the correlation between PB reduction mechanism and substrate are presented. (orig.)

  15. Evaluation on corrosively dissolved gold induced by alkanethiol monolayer with atomic absorption spectroscopy

    We have monitored a gold corrosive dissolution behavior accompanied in n-alkanethiol like n-dodecanethiol assembled process with in situ quartz crystal microbalance (QCM), and then observed it with atomic force microscopy (AFM) which showed an evident image of corrosive defects or holes produced on gold substrate, corresponding to gold dissolution induced by the alkanethiol molecules in the presence of oxygen. For detection of the dissolved gold defects during alkanethiol assembled process, an atomic absorption spectroscopy (AAS) has been carried out in this paper, and the detection limit for the dissolved gold could be evaluated to be 15.4 ng/mL. The amount of dissolved gold from the substrates of gold plates as functions of immersion time, acid media, solvents and thiol concentration has been examined in the oxygen saturated solutions. In comparison with in situ QCM method, the kinetics behavior of the long-term gold corrosion on the gold plates in 1.0 mmol/L of n-dodecanethiol solution determined with AAS method was a slow process, and its corrosion rate on gold dissolution could be evaluated to be about 4.4 x 10-5 ng.cm-2.s-1, corresponding to 1.3 x 108 Au atoms.cm-2.s-1, that was much smaller than that of initial rate monitored with in situ QCM. Both kinetics equations obtained with QCM and AAS showed a consistent corrosion behavior on gold surfaces.

  16. Some problems connected with boron determination by atomic absorption spectroscopy and the sensitivity improvement

    JELENA J. SAVOVIC

    2001-08-01

    Full Text Available Two atomizers were compared: an N2O–C2H2 flame and a stabilized U-shaped DC arc with aerosol supply. Both the high plasma temperature and the reducing atmosphere obtained by acetylene addition to the argon stream substantially increase the sensitivity of boron determination by atomic absorption spectroscopy (AAS when the arc atomizer is used. The results were compared with those for silicon as a control element. The experimental characteristic concentrations for both elements were compared with the computed values. The experimentally obtained characteristic concentration for boron when using the arc atomizer was in better agreement with the calculated value. It was estimated that the influence of stable monoxide formation on the sensitivity for both elements was about the same, but reduction of analyte and formation of non-volatile carbide particles was more important for boron, which is the main reason for the low sensitivity of boron determination using a flame atomizer. The use of an arc atomizer suppresses this interference and significantly improves the sensitivity of the determination.

  17. Ozone monitoring using differential optical absorption spectroscopy (DOAS) and UV photometry instruments in Sohar, Oman.

    Nawahda, Amin

    2015-08-01

    Ground level ozone (O3) concentrations were measured across Sohar highway in Oman during a four-month period from September to December 2014 by using an open-path deferential optical absorption spectroscopy (DOAS) instrument. The monthly average concentrations of O3 varied from 19.6 to 29.4 ppb. The measurements of O3 are compared with the measurements of a non-open-path UV photometry analyzer (UVP). The percent difference (PD) concept and linear regression methods were used to compare the readings of the two instruments. The findings show high correlation coefficients between the measurements of the DOAS and UVP instruments. The DOAS measurements of O3 are found to be less than those measured by the UVP instrument; the correlation coefficients between absolute PD values and meteorological parameters and PM2.5 were very low indicating a minor effect; therefore, titrations of O3 by traffic emissions and difference in elevation could be the reason for the difference in the measurements of the two instruments. PMID:26138853

  18. A Semi-Blind Source Separation Method for Differential Optical Absorption Spectroscopy of Atmospheric Gas Mixtures

    Sun, Y; Finlayson-Pitts, B J; Xin, J

    2011-01-01

    Differential optical absorption spectroscopy (DOAS) is a powerful tool for detecting and quantifying trace gases in atmospheric chemistry \\cite{Platt_Stutz08}. DOAS spectra consist of a linear combination of complex multi-peak multi-scale structures. Most DOAS analysis routines in use today are based on least squares techniques, for example, the approach developed in the 1970s uses polynomial fits to remove a slowly varying background, and known reference spectra to retrieve the identity and concentrations of reference gases. An open problem is to identify unknown gases in the fitting residuals for complex atmospheric mixtures. In this work, we develop a novel three step semi-blind source separation method. The first step uses a multi-resolution analysis to remove the slow-varying and fast-varying components in the DOAS spectral data matrix $X$. The second step decomposes the preprocessed data $\\hat{X}$ in the first step into a linear combination of the reference spectra plus a remainder, or $\\hat{X} = A\\,S +...

  19. Vibration-rotational overtones absorption of solid hydrogens using optoacoustic spectroscopy technique

    Vibrational-rotational overtones absorption solid hydrogens (H2, D2, HD) is studied using pulsed laser piezoeletric transducer (PULPIT) optoacoustic spectroscopy is studied. A general downward shift in energy from isolated molecular energies is observed. Studying normal-hydrogen it was observed that the phonon excitations associated with double-molecular transitions are predominantly transverse-optical phonons, whereas the excitations associated with single-molecular transitions are predominantly longitudinal - optical phonons. Multiplet structures were observed for certain double transitions in parahydrogen and orthodeuterium. The HD spectrum, besides presenting the sharp zero-phonon lines and the associated phonon side bands, like H2 and D2, showed also two different features. This observation was common to all the transitions involving pure rotational excitation in H2 and D2, which showed broad linewidths. This, together with some other facts (fluorescence lifetime *approx*105 sec; weak internal vibration and lattice coupling), led to the proposition of a mechanism for the fast nonradiative relaxation in solid hydrogens, implied from some observed experimental evidences. This relaxation, due to strong coupling, would happen in two steps: the internal vibration modes would relax to the rotational modes of the molecules, and then this rotational modes would relax to the lattice vibration modes. (Author)

  20. A multi-channel monolithic Ge detector system for fluorescence x-ray absorption spectroscopy

    Bucher, J.J.; Allen, P.G.; Edelstein, N.M.; Shuh, D.K. [Lawrence Berkeley National Lab., CA (United States). Chemical Sciences Div.; Madden, N.W.; Cork, C.; Luke, P.; Pehl, D.; Malone, D. [Lawrence Berkeley National Lab., CA (United States). Engineering Div.

    1995-03-01

    Construction and performance of a monolithic quad-pixel Ge detector for fluorescence x-ray absorption spectroscopy (XAS) at synchrotron radiation sources are described. The detector semiconductor element has an active surface area of 4.0 cm{sup 2} which is electrically separated into four 1.0 cm{sup 2} pixels, with little interfacial dead volume. Spatial response of the array shows that cross-talk between adjacent pixels is < 10% for 5.9 keV photons that fall within 0.5 mm of the pixel boundaries. The detector electronics system uses pre-amplifiers built at LBNL with commercial Tennelec Model TC 244 amplifiers. Using an {sup 55}Fe test source (MnK{sub {alpha}}, 5.9 keV), energy resolution of better than 200 eV is achieved with a 4 {mu}sec peaking time. At 0.5 {mu}sec peaking time, pulse pileup results in a 75% throughput efficiency for an incoming count rate of 100 kHz. Initial XAS fluoresncece measurements at the beamline 4 wiggler end stations at SSRL show that the detector system has several advantages over commercial x-ray spectrometers for low-concentration counting.

  1. Probing the chemical reactivity of free titanium clusters by X-ray absorption spectroscopy

    Synchrotron radiation-based experimental techniques are largely employed for the characterization of the reactivity of finite size systems; in particular, X-ray absorption spectroscopy (XAS) is a suitable tool to shed light on the local electronic structure and chemical status of atoms in nano-objects, as it is very sensitive to the local bonding environment of the probed site. In supported clusters intrinsic properties and reactivity are largely distorted and obscured by the changes imposed by the growth procedure and by the influence of the substrate, so the attainability of experiments on free clusters reacting with species in the gas phase is a primary goal in the development of cluster science. In this paper we report a proof of principle of the applicability of gas phase XAS technique to titanium and titanium oxide, hydride and hydrate systems. Experiments are performed by coupling a pulsed microplasma cluster source (PMCS) with a third generation synchrotron light source, and measuring the intensity of the electron yield coming from the interaction of VUV photons with the clusters seeded in a supersonic beam. (orig.)

  2. The high-resolution absorption spectroscopy branch on the VUV beamline DESIRS at SOLEIL.

    de Oliveira, Nelson; Joyeux, Denis; Roudjane, Mourad; Gil, Jean François; Pilette, Bertrand; Archer, Lucy; Ito, Kenji; Nahon, Laurent

    2016-07-01

    A VUV absorption spectroscopy facility designed for ultra-high spectral resolution is in operation as a dedicated branch on the DESIRS beamline at Synchrotron SOLEIL. This branch includes a unique VUV Fourier transform spectrometer (FTS) and a dedicated versatile gas sample chamber. The FTS instrument can cover a large UV-VUV spectral range from 4 to 30 eV, with an ultimate line width of 0.08 cm(-1) on a large spectral window, ΔE/E = 7%, over which all spectral features can be acquired in a multiplex way. The performance can be considered to be a middle ground between broadband moderate-resolution spectrometers based on gratings and ultra-high-spectral-resolution VUV tunable-laser-based techniques over very narrow spectral windows. The various available gaseous-sample-handling setups, which function over a wide range of pressures and temperatures, and the acquisition methodology are described. A selection of experimental results illustrates the performance and limitations of the FTS-based facility. PMID:27359137

  3. Communication: Hydrogen bonding interactions in water-alcohol mixtures from X-ray absorption spectroscopy

    Lam, Royce K.; Smith, Jacob W.; Saykally, Richard J.

    2016-05-01

    While methanol and ethanol are macroscopically miscible with water, their mixtures exhibit negative excess entropies of mixing. Despite considerable effort in both experiment and theory, there remains significant disagreement regarding the origin of this effect. Different models for the liquid mixture structure have been proposed to address this behavior, including the enhancement of the water hydrogen bonding network around the alcohol hydrophobic groups and microscopic immiscibility or clustering. We have investigated mixtures of methanol, ethanol, and isopropanol with water by liquid microjet X-ray absorption spectroscopy on the oxygen K-edge, an atom-specific probe providing details of both inter- and intra-molecular structure. The measured spectra evidence a significant enhancement of hydrogen bonding originating from the methanol and ethanol hydroxyl groups upon the addition of water. These additional hydrogen bonding interactions would strengthen the liquid-liquid interactions, resulting in additional ordering in the liquid structures and leading to a reduction in entropy and a negative enthalpy of mixing, consistent with existing thermodynamic data. In contrast, the spectra of the isopropanol-water mixtures exhibit an increase in the number of broken alcohol hydrogen bonds for mixtures containing up to 0.5 water mole fraction, an observation consistent with existing enthalpy of mixing data, suggesting that the measured negative excess entropy is a result of clustering or micro-immiscibility.

  4. Electronic structures of silicon monoxide film probed by X-ray absorption spectroscopy

    Baba, Yuji; Sekiguchi, Tetsuhiro; Shimoyama, Iwao; Hirao, Norie

    2013-06-01

    Electronic structures of thin films of silicon monoxides (SiO) deposited on a solid surface have been in-situ investigated by X-ray photoelectron spectroscopy (XPS) and X-ray absorption fine structure (XAFS). As a substrate, a highly oriented pyrolytic graphite (HOPG) was used because the hybridization between molecules and substrate can be excluded due to the inertness of the surface. For thin films with less than monolayer, XPS spectrum showed that the binding energy of the Si 1s is located just between those of the elemental silicon (Si0) and SiO2 (Si4 +). The result indicates that the stable divalent silicon surely exists in the deposited SiO layer. For the Si K-edge XAFS spectrum of the SiO thin film, the energy of the core-to-valence resonance peak is also located between those of the elemental silicon (Si0) and SiO2 (Si4 +). The polarization dependence of the Si K-edge XAFS spectra for the SiO film revealed that the SiO molecules are well-ordered and almost perpendicularly oriented on HOPG surface. The XAFS results also support the existence of the silicon divalent states in the deposited SiO films. The obtained well-ordered SiO films with divalent silicon will become an excellent starting material for the synthesis of low-dimensional SiOx films.

  5. Summertime measurements of benzene and toluene in Athens using a differential optical absorption spectroscopy system.

    Petrakis, Michael; Psiloglou, Basil; Kassomenos, Pavlos A; Cartalis, Costas

    2003-09-01

    In this paper, measurements of benzene, toluene, p,m-xylene, ozone (O3), nitrogen dioxide (NO2), and sulfur dioxide (SO2) made using the differential optical absorption spectroscopy (DOAS) technique during a 4-month period of summer 2000 (June-September) in Athens, Greece, are presented. An assessment of benzene mean value concentrations during this 4-month period exceeded 10 microg/m3, which is 2 times greater than the average yearly limit proposed by European authorities. Toluene measurements present mean values of approximately 33 microg/m3. Benzene and especially toluene measurements are highly correlated with NO2 and anticorrelated with O3. High values of benzene, NO2, and toluene are also correlated with winds from the southeast section, an area of industrial activity where emissions of volatile organic compounds (VOCs) have been recorded in previous studies. O3 is correlated with winds from the south-southwest section affected by the sea breeze circulation. Diurnal variations of O3, NO2, and SO2 concentrations are compatible with measurements from the stations of the Ministry of Environment's network. Outliers are combined with weak winds from the south-southwest. As far as p,m-xylene measurements are concerned, there is a poor correlation between gas chromatography (GC) and DOAS Opsis measurements, also observed in previous relevant campaigns and eventually a criticism in the use of the DOAS Opsis model for the measurement of p,m-xylene. PMID:13678363

  6. Applicability of light-emitting diodes as light sources for active differential optical absorption spectroscopy measurements.

    Kern, Christoph; Trick, Sebastian; Rippel, Bernhard; Platt, Ulrich

    2006-03-20

    We present what is to our knowledge the first use of light-emitting diodes (LEDs) as light sources for long-path differential optical absorption spectroscopy (LP-DOAS) measurements of trace gases in the open atmosphere. Modern LEDs represent a potentially advantageous alternative to thermal light sources, in particular to xenon arc lamps, which are the most common active DOAS light sources. The radiative properties of a variety of LEDs were characterized, and parameters such as spectral shape, spectral range, spectral stability, and ways in which they can be influenced by environmental factors were analyzed. The spectra of several LEDs were found to contain Fabry-Perot etalon-induced spectral structures that interfered with the DOAS evaluation, in particular when a constant temperature was not maintained. It was shown that LEDs can be used successfully as light sources in active DOAS experiments that measure NO2 and NO3 near 450 and 630 nm, respectively. Average detection limits of 0.3 parts in 10(9) and 16 parts in 10(12) respectively, were obtained by use of a 6 km light path in the open atmosphere. PMID:16579579

  7. Total Absorption Spectroscopy of Fission Fragments Relevant for Reactor Antineutrino Spectra and Decay Heat Calculations

    Porta A.

    2016-01-01

    Full Text Available Beta decay of fission products is at the origin of decay heat and antineutrino emission in nuclear reactors. Decay heat represents about 7% of the reactor power during operation and strongly impacts reactor safety. Reactor antineutrino detection is used in several fundamental neutrino physics experiments and it can also be used for reactor monitoring and non-proliferation purposes. 92,93Rb are two fission products of importance in reactor antineutrino spectra and decay heat, but their β-decay properties are not well known. New measurements of 92,93Rb β-decay properties have been performed at the IGISOL facility (Jyväskylä, Finland using Total Absorption Spectroscopy (TAS. TAS is complementary to techniques based on Germanium detectors. It implies the use of a calorimeter to measure the total gamma intensity de-exciting each level in the daughter nucleus providing a direct measurement of the beta feeding. In these proceedings we present preliminary results for 93Rb, our measured beta feedings for 92Rb and we show the impact of these results on reactor antineutrino spectra and decay heat calculations.

  8. Total Absorption Spectroscopy of Fission Fragments Relevant for Reactor Antineutrino Spectra and Decay Heat Calculations

    Porta, A.; Zakari-Issoufou, A.-A.; Fallot, M.; Algora, A.; Tain, J. L.; Valencia, E.; Rice, S.; Bui, V. M.; Cormon, S.; Estienne, M.; Agramunt, J.; Äystö, J.; Bowry, M.; Briz, J. A.; Caballero-Folch, R.; Cano-Ott, D.; Cucouanes, A.; Elomaa, V.-V.; Eronen, T.; Estévez, E.; Farrelly, G. F.; Garcia, A. R.; Gelletly, W.; Gomez-Hornillos, M. B.; Gorlychev, V.; Hakala, J.; Jokinen, A.; Jordan, M. D.; Kankainen, A.; Karvonen, P.; Kolhinen, V. S.; Kondev, F. G.; Martinez, T.; Mendoza, E.; Molina, F.; Moore, I.; Perez-Cerdán, A. B.; Podolyák, Zs.; Penttilä, H.; Regan, P. H.; Reponen, M.; Rissanen, J.; Rubio, B.; Shiba, T.; Sonzogni, A. A.; Weber, C.

    2016-03-01

    Beta decay of fission products is at the origin of decay heat and antineutrino emission in nuclear reactors. Decay heat represents about 7% of the reactor power during operation and strongly impacts reactor safety. Reactor antineutrino detection is used in several fundamental neutrino physics experiments and it can also be used for reactor monitoring and non-proliferation purposes. 92,93Rb are two fission products of importance in reactor antineutrino spectra and decay heat, but their β-decay properties are not well known. New measurements of 92,93Rb β-decay properties have been performed at the IGISOL facility (Jyväskylä, Finland) using Total Absorption Spectroscopy (TAS). TAS is complementary to techniques based on Germanium detectors. It implies the use of a calorimeter to measure the total gamma intensity de-exciting each level in the daughter nucleus providing a direct measurement of the beta feeding. In these proceedings we present preliminary results for 93Rb, our measured beta feedings for 92Rb and we show the impact of these results on reactor antineutrino spectra and decay heat calculations.

  9. X-ray absorption spectroscopy of lithium sulfur battery reaction intermediates

    Wujcik, Kevin; Pascal, Tod; Prendergast, David; Balsara, Nitash

    2015-03-01

    Lithium sulfur batteries have a theoretical energy density nearly five times greater than current lithium ion battery standards, but questions still remain regarding the reaction pathways through which soluble lithium polysulfide (Li2Sx, ``x'' ranging from 2 to 8) reaction intermediates are formed. Complicating spectroelectrochemical approaches to elucidate redox pathways is the challenge of obtaining spectral standards for individual Li2Sx species. Lithium polysulfides cannot be isolated as individual component and exist only in solution as a distribution of different Li2Sx molecules formed via disproportionation reactions (e.g. 2Li2S4 goes to Li2S3 + Li2S5). X-ray absorption spectroscopy (XAS) at the sulfur K-edge has recently been employed as a technique to study Li-S chemistry. We have recently obtained XAS standards for individual Li2Sx species via first principles DFT simulations and the excited electron and core hole approach. Here, experimental sulfur K-edge XAS of Li2Sx species dissolved in poly(ethylene oxide) are compared to spectra obtained from analogous theoretical calculations. The impact that polysulfide solution concentration and the presence of other lithium salts (e.g. LiNO3) have on X-ray spectra of Li2Sx species is explored via experiment and theory.

  10. X-ray absorption spectroscopy study of the titania- and alumina-supported tungsten oxide system

    Tungsten oxide supported on titania is an important material for the selective catalytic reduction of nitrogen oxides NOx. A structure analysis by means of X-ray absorption spectroscopy (XANES and EXAFS) is reported for materials prepared by spreading of WO3 in physical mixtures with the support oxide as well as by impregnation from aqueous solution. A comparison is also made with alumina-supported materials. Analysis of the XANES region at the W L1 and W L3 edges indicated that tungsten is hexavalent and anchored to the surface as WO5 and WO4 units, the relative proportion of which increases with loading. When water is absorbed, pseudooctahedrally coordinated species are formed in both cases. The analysis of the EXAFS provides additional support for the existence of these structures, which contain oxo groups W double-bond O and W-O-W bridges. A tentative structure model is proposed, in which islands of surface tungstate species are formed by branched chains of WO5 units. The chains are assumed to be terminated by WO4 units, the WO5/WO4 ratio thus increasing with chain length or island size, which obviously increases with loading

  11. Assessment of the performance of a compact concentric spectrometer system for Atmospheric Differential Optical Absorption Spectroscopy

    C. Whyte

    2009-08-01

    Full Text Available A breadboard demonstrator of a novel UV/VIS grating spectrometer for atmospheric research has been developed based upon a concentric arrangement of a spherical meniscus lens, concave spherical mirror and curved diffraction grating suitable for a range of remote sensing applications from the ground or space. The spectrometer is compact and provides high optical efficiency and performance benefits over traditional instruments. The concentric design is capable of handling high relative apertures, owing to spherical aberration and coma being near zero at all surfaces. The design also provides correction for transverse chromatic aberration and distortion, in addition to correcting for the distortion called "smile", the curvature of the slit image formed at each wavelength. These properties render this design capable of superior spectral and spatial performance with size and weight budgets significantly lower than standard configurations. This form of spectrometer design offers the potential for an exceptionally compact instrument for differential optical absorption spectroscopy (DOAS applications particularly from space (LEO, GEO orbits and from HAPs or ground-based platforms. The breadboard demonstrator has been shown to offer high throughput and a stable Gaussian line shape with a spectral range from 300 to 450 nm at better than 0.5 nm resolution, suitable for a number of typical DOAS applications.

  12. Assessment of the performance of a compact concentric spectrometer system for Atmospheric Differential Optical Absorption Spectroscopy

    C. Whyte

    2009-12-01

    Full Text Available A breadboard demonstrator of a novel UV/VIS grating spectrometer has been developed based upon a concentric arrangement of a spherical meniscus lens, concave spherical mirror and curved diffraction grating suitable for a range of atmospheric remote sensing applications from the ground or space. The spectrometer is compact and provides high optical efficiency and performance benefits over traditional instruments. The concentric design is capable of handling high relative apertures, owing to spherical aberration and comma being near zero at all surfaces. The design also provides correction for transverse chromatic aberration and distortion, in addition to correcting for the distortion called "smile", the curvature of the slit image formed at each wavelength. These properties render this design capable of superior spectral and spatial performance with size and weight budgets significantly lower than standard configurations. This form of spectrometer design offers the potential for exceptionally compact instrument for differential optical absorption spectroscopy (DOAS applications from LEO, GEO, HAP or ground-based platforms. The breadboard demonstrator has been shown to offer high throughput and a stable Gaussian line shape with a spectral range from 300 to 450 nm at 0.5 nm resolution, suitable for a number of typical DOAS applications.

  13. X-ray absorption spectroscopy study on the thermal and hydrazine reduction of graphene oxide

    Liang, Xianqing, E-mail: lxq@gxu.edu.cn [The Colleague of Physics Science and Technology, Guangxi University, Nanning 530004 (China); Wang, Yu [National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230029 (China); Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201204 (China); Zheng, Huiyuan [The Colleague of Physics Science and Technology, Guangxi University, Nanning 530004 (China); Wu, Ziyu, E-mail: wuzy@ustc.edu.cn [National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230029 (China)

    2014-10-15

    Highlights: • XAS study of GO and reduced GO was performed. • Detailed evolution of the electronic structures and chemical bonding of GO was revealed. • A new efficient route for the reduction of GO is proposed. - Abstract: X-ray absorption spectroscopy (XAS) was applied to systemically investigate the deoxygenation of graphene oxide (GO) via annealing and hydrazine treatment. Detailed evolution of the electronic structures and chemical bonding of GO was presented. The enhanced intensity of π{sup *} resonance and the appearance of splitting σ{sup *} resonance in C K-edge XAS spectra suggest high extents of recoveries of π-conjugation upon reduction using thermal annealing or hydrazine. Experimental results revealed that the carboxyl as well as epoxide and hydroxyl groups on the surface of GO were thermally reduced first, followed by the more difficult removal of carbonyl and cyclic ether groups at higher temperatures. The hydrazine reduction could remove epoxide, hydroxyl and carboxyl groups effectively, whereas the carbonyl groups were partially reduced with the incorporation of nitrogen species simultaneously. The residual oxygen functional groups on hydrazine-reduced GO could be further removed after modest thermal annealing. It was proposed that a combination of both types of reductions would give the best deoxygenation efficiency for the production of graphene.

  14. Accurate measurement of the HI column density from HI 21cm absorption-emission spectroscopy

    Chengalur, Jayaram N; Roy, Nirupam

    2013-01-01

    We present a detailed study of an estimator of the HI column density, based on a combination of HI 21cm absorption and HI 21cm emission spectroscopy. This "isothermal" estimate is given by $N_{\\rm HI,ISO} = 1.823 \\times 10^{18} \\int \\left[ \\tau_{\\rm tot} \\times {\\rm T_B} \\right] / \\left[ 1 - e^{-\\tau_{\\rm tot}} \\right] {\\rm dV}$, where $\\tau_{\\rm tot}$ is the total HI 21cm optical depth along the sightline and ${\\rm T_B}$ is the measured brightness temperature. We have used a Monte Carlo simulation to quantify the accuracy of the isothermal estimate by comparing the derived $N_{\\rm HI,ISO}$ with the true HI column density $N_{\\rm HI}$. The simulation was carried out for a wide range of sightlines, including gas in different temperature phases and random locations along the path. We find that the results are statistically insensitive to the assumed gas temperature distribution and the positions of different phases along the line of sight. The median value of the ratio of the true H{\\sc i} column density to the...

  15. Standoff gas leak detectors based on tunable diode laser absorption spectroscopy

    Frish, M. B.; Wainner, R. T.; Green, B. D.; Laderer, M. C.; Allen, M. G.

    2005-11-01

    Trace gas sensing and analysis by Tunable Diode Laser Absorption Spectroscopy (TDLAS) has become a robust and reliable technology accepted for industrial process monitoring and control, quality assurance, environmental sensing, plant safety, and infrastructure security. Sensors incorporating well-packaged wavelength-stabilized near-infrared (1.2 to 2.0 μm) laser sources sense over a dozen toxic or industrially-important gases. A large emerging application for TDLAS is standoff sensing of gas leaks, e.g. from natural gas pipelines. The Remote Methane Leak Detector (RMLD), a handheld standoff TDLAS leak survey tool that we developed, is replacing traditional leak detection tools that must be physically immersed within a leak to detect it. Employing a 10 mW 1.6 micron DFB laser, the RMLD illuminates a non-cooperative topographic surface, up to 30 m distant, and analyzes returned scattered light to deduce the presence of excess methane. The eye-safe, battery-powered, 6-pound handheld RMLD enhances walking pipeline survey rates by more than 30%. When combined with a spinning or rastering mirror, the RMLD serves as a platform for mobile leak mapping systems. Also, to enable high-altitude surveying and provide aerial disaster response, we are extending the standoff range to 3000 m by adding an EDFA to the laser transmitter.

  16. Properties of aqueous nitrate and nitrite from x-ray absorption spectroscopy

    Smith, Jacob W.; Lam, Royce K.; Saykally, Richard J., E-mail: saykally@berkeley.edu [Department of Chemistry, University of California, Berkeley, California 94720 (United States); Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States); Shih, Orion [National Synchrotron Radiation Research Center, Hsinchu 30076, Taiwan (China); Rizzuto, Anthony M. [Department of Chemistry, University of California, Berkeley, California 94720 (United States); Prendergast, David [The Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States)

    2015-08-28

    Nitrate and nitrite ions are of considerable interest, both for their widespread use in commercial and research contexts and because of their central role in the global nitrogen cycle. The chemistry of atmospheric aerosols, wherein nitrate is abundant, has been found to depend on the interfacial behavior of ionic species. The interfacial behavior of ions is determined largely by their hydration properties; consequently, the study of the hydration and interfacial behavior of nitrate and nitrite comprises a significant field of study. In this work, we describe the study of aqueous solutions of sodium nitrate and nitrite via X-ray absorption spectroscopy (XAS), interpreted in light of first-principles density functional theory electronic structure calculations. Experimental and calculated spectra of the nitrogen K-edge XA spectra of bulk solutions exhibit a large 3.7 eV shift between the XA spectra of nitrate and nitrite resulting from greater stabilization of the nitrogen 1s energy level in nitrate. A similar shift is not observed in the oxygen K-edge XA spectra of NO{sub 3}{sup −} and NO{sub 2}{sup −}. The hydration properties of nitrate and nitrite are found to be similar, with both anions exhibiting a similar propensity towards ion pairing.

  17. Properties of aqueous nitrate and nitrite from x-ray absorption spectroscopy

    Smith, Jacob W.; Lam, Royce K.; Shih, Orion; Rizzuto, Anthony M.; Prendergast, David; Saykally, Richard J.

    2015-08-01

    Nitrate and nitrite ions are of considerable interest, both for their widespread use in commercial and research contexts and because of their central role in the global nitrogen cycle. The chemistry of atmospheric aerosols, wherein nitrate is abundant, has been found to depend on the interfacial behavior of ionic species. The interfacial behavior of ions is determined largely by their hydration properties; consequently, the study of the hydration and interfacial behavior of nitrate and nitrite comprises a significant field of study. In this work, we describe the study of aqueous solutions of sodium nitrate and nitrite via X-ray absorption spectroscopy (XAS), interpreted in light of first-principles density functional theory electronic structure calculations. Experimental and calculated spectra of the nitrogen K-edge XA spectra of bulk solutions exhibit a large 3.7 eV shift between the XA spectra of nitrate and nitrite resulting from greater stabilization of the nitrogen 1s energy level in nitrate. A similar shift is not observed in the oxygen K-edge XA spectra of NO3- and NO2-. The hydration properties of nitrate and nitrite are found to be similar, with both anions exhibiting a similar propensity towards ion pairing.

  18. X-ray absorption spectroscopy: EXAFS and XANES - A versatile tool to study the atomic and electronic structure of materials

    X-ray absorption spectroscopy (XAS) had been an essential tool to gather spectroscopic information about atomic energy level structure in the early decades of this century. The correct interpretation of the oscillatory structure in the x-ray absorption cross-section above the absorption edge has transformed XAS from a spectroscopic tool to a structural technique. EXAFS (Extended X-ray Absorption Fine Structure) yields information about the interatomic distances, near neighbor coordination numbers, and lattice dynamics. XANES (X-ray Absorption Near Edge Structure), on the other hand, gives information about the valence state, energy bandwidth and bond angles. Today, there are about 50 experimental stations in various synchrotrons around the world dedicated to collecting x-ray absorption data from the bulk and surfaces of solids and liquids. In this chapter, they will give the basic principles of XAS, explain the information content of essentially two different aspects of the absorption process leading to EXAFS and XANES, and discuss the source and sample limitations

  19. Quantum cascade laser absorption spectroscopy with the amplitude-to-time conversion technique for atmospheric-pressure plasmas

    The NO2 concentration, i.e., density, in a small plasma of a nitrogen oxide (NOx) treatment reactor has been measured by highly sensitive laser absorption spectroscopy. The absorption spectroscopy uses a single path of a quantum cascade laser beam passing through a plasma whose dimension is about 1 cm. The high sensitivity of spectroscopy is achieved by the amplitude-to-time conversion technique. Although the plasma reactor is designed to convert NO in the input gas to NO2, it has been demonstrated by this highly sensitive absorption spectroscopy that NO2 in a simulated exhaust gas that enters the reactor is decomposed by the plasma first and then NO2 is formed again, possibly more than it was decomposed, through a series of gas-phase reactions by the time the gas exits the reactor. The observation is consistent with that of an earlier study on NO decomposition by the same type of a plasma reactor [T. Yumii et al., J. Phys. D 46, 135202 (2013)], in which a high concentration of NO2 was observed at the exit of the reactor.

  20. Quantum cascade laser absorption spectroscopy with the amplitude-to-time conversion technique for atmospheric-pressure plasmas

    Yumii, Takayoshi; Kimura, Noriaki [Mitsui Engineering and Shipbuilding Co., Ltd., Tamahara 3-16-1, Tamano, Okayama 706-0014 (Japan); Graduate School of Engineering, Osaka University, Yamadaoka 2-1, Suita, Osaka 565-0871 (Japan); Hamaguchi, Satoshi [Graduate School of Engineering, Osaka University, Yamadaoka 2-1, Suita, Osaka 565-0871 (Japan)

    2013-06-07

    The NO{sub 2} concentration, i.e., density, in a small plasma of a nitrogen oxide (NOx) treatment reactor has been measured by highly sensitive laser absorption spectroscopy. The absorption spectroscopy uses a single path of a quantum cascade laser beam passing through a plasma whose dimension is about 1 cm. The high sensitivity of spectroscopy is achieved by the amplitude-to-time conversion technique. Although the plasma reactor is designed to convert NO in the input gas to NO{sub 2}, it has been demonstrated by this highly sensitive absorption spectroscopy that NO{sub 2} in a simulated exhaust gas that enters the reactor is decomposed by the plasma first and then NO{sub 2} is formed again, possibly more than it was decomposed, through a series of gas-phase reactions by the time the gas exits the reactor. The observation is consistent with that of an earlier study on NO decomposition by the same type of a plasma reactor [T. Yumii et al., J. Phys. D 46, 135202 (2013)], in which a high concentration of NO{sub 2} was observed at the exit of the reactor.

  1. Bimetallic Catalysts and Platinum Surfaces Studied by X-ray Absorption Spectroscopy and Scanning Tunnelling Microscopy

    Roenning, Magnus

    2000-07-01

    Bimetallic catalyst systems used in Fischer-Tropsch synthesis (Co-Re/Al{sub 2}O{sub 3}) and in the naphtha reforming process (Pt-Re/Al{sub 2}O{sub 3}) have been studied in situ using X-ray absorption spectroscopy (EXAFS). Additionally, the adsorption of ethene on platinum single crystal surfaces has been investigated using scanning tunnelling microscopy. In situ EXAFS at the cobalt K absorption edge have been carried out at 450{sup o}C on the hydrogen reduction of a rhenium-promoted Co{sub 3}O{sub 4}/Al{sub 2}O{sub 3} catalyst. Reductions carried out using 100% hydrogen and 5% hydrogen in helium gave different results. Whereas the reduction using dilute hydrogen leads to bulk-like metallic cobalt particles (hcp or fcc), reaction with pure hydrogen yields a more dispersed system with smaller cobalt metal particles (< 40 A). The results are rationalised in terms of different degrees of reoxidation of cobalt by the higher and lower concentrations of water generated during the reduction of cobalt oxide by 100% and 5% hydrogen, respectively. Additionally, in both reduction protocols a small fraction (3 -4 wt%) of the cobalt content is randomly dispersed over the tetrahedral vacancies of the alumina support. This dispersion occurs during reduction and not calcination. The cobalt in these sites cannot be reduced at 450 {sup o}C. The local environments about the rhenium atoms in Co-Re/{gamma}-A1{sub 2}O{sub 3} catalyst after different reduction periods have been studied by X-ray absorption spectroscopy. A bimetallic catalyst containing 4.6 wt% cobalt and 2 wt% rhenium has been compared with a corresponding monometallic sample with 2 wt% rhenium on the same support. The rhenium L{sub III} EXAFS analysis shows that bimetallic particles are formed after reduction at 450{sup o}C with the average particle size being 10-15 A. Rhenium is shown to be reduced at a later stage than cobalt. The fraction of cobalt atoms entering the support obstructs the access to the support for the

  2. Bimetallic Catalysts and Platinum Surfaces Studied by X-ray Absorption Spectroscopy and Scanning Tunnelling Microscopy

    Roenning, Magnus

    2000-07-01

    Bimetallic catalyst systems used in Fischer-Tropsch synthesis (Co-Re/Al{sub 2}O{sub 3}) and in the naphtha reforming process (Pt-Re/Al{sub 2}O{sub 3}) have been studied in situ using X-ray absorption spectroscopy (EXAFS). Additionally, the adsorption of ethene on platinum single crystal surfaces has been investigated using scanning tunnelling microscopy. In situ EXAFS at the cobalt K absorption edge have been carried out at 450{sup o}C on the hydrogen reduction of a rhenium-promoted Co{sub 3}O{sub 4}/Al{sub 2}O{sub 3} catalyst. Reductions carried out using 100% hydrogen and 5% hydrogen in helium gave different results. Whereas the reduction using dilute hydrogen leads to bulk-like metallic cobalt particles (hcp or fcc), reaction with pure hydrogen yields a more dispersed system with smaller cobalt metal particles (< 40 A). The results are rationalised in terms of different degrees of reoxidation of cobalt by the higher and lower concentrations of water generated during the reduction of cobalt oxide by 100% and 5% hydrogen, respectively. Additionally, in both reduction protocols a small fraction (3 -4 wt%) of the cobalt content is randomly dispersed over the tetrahedral vacancies of the alumina support. This dispersion occurs during reduction and not calcination. The cobalt in these sites cannot be reduced at 450 {sup o}C. The local environments about the rhenium atoms in Co-Re/{gamma}-A1{sub 2}O{sub 3} catalyst after different reduction periods have been studied by X-ray absorption spectroscopy. A bimetallic catalyst containing 4.6 wt% cobalt and 2 wt% rhenium has been compared with a corresponding monometallic sample with 2 wt% rhenium on the same support. The rhenium L{sub III} EXAFS analysis shows that bimetallic particles are formed after reduction at 450{sup o}C with the average particle size being 10-15 A. Rhenium is shown to be reduced at a later stage than cobalt. The fraction of cobalt atoms entering the support obstructs the access to the support for the

  3. X-ray absorption spectroscopy of Mn doped ZnO thin films prepared by rf sputtering technique

    A set of r.f. sputter deposited ZnO thin films prepared with different Mn doping concentrations have been characterised by Extended X-ray Absorption Fine Structure (EXAFS) and X-ray Absorption Near Edge Spectroscopy (XANES) measurements at Zn, Mn and O K edges and at Mn L2,3 edges apart from long range structural characterisation by Grazing Incident X-ray Diffraction (GIXRD) technique. Magnetic measurements show room temperature ferromagnetism in samples with lower Mn doping which is however, gets destroyed at higher Mn doping concentration. The results of the magnetic measurements have been explained using the local structure information obtained from EXAFS and XANES measurements

  4. Absolute photo-absorption cross sections and electronic state spectroscopy of selected fluorinated hydrocarbons relevant to the plasma processing industry

    Photo-absorption cross sections have been measured for methyl iodide, CF3I (310 nm>λ>110 nm) and dichlorodifluoromethane, CCl2F2 (225 nm>λ>110 nm) using synchrotron radiation. Electron energy loss spectroscopy was also used to probe the electronic and vibronic excitation of CF3I. Electronic states have been assigned to each of the observed absorption bands incorporating both valence and Rydberg transitions. The measured VUV cross sections are used to derive the photolysis rates in the terrestrial atmosphere and hence determine the potential importance of each gas in global warming and ozone depletion

  5. Formation of host–guest complexes on gold surface investigated by surface-enhanced IR absorption spectroscopy

    Inokuchi, Yoshiya; Mizuuchi, Takahiro; Ebata, Takayuki; Ikeda, Toshiaki; Haino, Takeharu; Kimura, Tetsunari; Guo, Hao; Furutani, Yuji

    2014-01-01

    We apply surface-enhanced infrared absorption (SEIRA) spectroscopy to host-guest complexes in liquid phase to examine the structural change in the complex formation. Two thiol derivatives of 18-crown-6 (18C6) are chemisorbed on a gold surface, and aqueous solutions of MCl salts (M = Li, Na, K, Rb, and Cs) are put to form M+・18C6 complexes. Infrared spectra of these complexes in the 900-2000 cm-1 region are obtained by SEIRA spectroscopy. The observed IR spectra show noticeable peaks due to th...

  6. Fourier transform infrared reflection absorption spectroscopy and microspectroscopy, a tool to investigate thermally grown oxide scales

    Lefez, B. [Institut des Materiaux de Rouen, LASTSM, Universite de Rouen, UPRES-EA 1290, 76801 Saint Etienne du Rouvray Cedex (France)], E-mail: benoit.lefez@univ-rouen.fr; Lopitaux, J.; Hannoyer, B. [Institut des Materiaux de Rouen, LASTSM, Universite de Rouen, UPRES-EA 1290, 76801 Saint Etienne du Rouvray Cedex (France); Bacos, M.-P. [Office National d' Etudes et de Recherches Aerospatiales (ONERA), BP 72-29, Avenue de la Division Leclerc, 92322 Chatillon Cedex (France); Beucher, E. [CRITT Analyses et surface, Site Industriel des Jonquets-2 chemin du Roy, 27400, Louviers (France)

    2007-12-03

    The main goal of this work is to show the interesting contribution of reflectance infrared spectroscopy to determine the composition of oxide films on metal surfaces. Illustration is reported on oxidation of {alpha}{sub 2}-TiAl (Ti75-Al25 at.%) and {gamma}-TiAl (Ti50-Al50 at.%) alloys, carried out at 650 deg. C under laboratory atmosphere. Reflectance infrared spectra were recorded on an FTIR 710 Nicolet spectrophotometer, equipped with a Nicolet IR plan microscope. The knowledge of the infrared optical constants makes it possible to predict the infrared reflection spectra of different thin layers. As there is a lack of data in literature, theoretical calculations have been made in order to study experimental spectra. To illustrate these computations the first band observed for a thin film (200 nm) of Al{sub 2}O{sub 3} is the higher longitudinal optical (LO) mode, the position of which is 920 cm{sup -1} for {alpha}-Al{sub 2}O{sub 3}, 930 cm{sup -1} for {gamma}-Al{sub 2}O{sub 3} or a broad band at 980 cm{sup -1} for amorphous Al{sub 2}O{sub 3}. In the case of TiO{sub 2}/alloy system, the LO mode moves from 830 cm{sup -1} for rutile TiO{sub 2} to 880 cm{sup -1} for anatase TiO{sub 2}. A peak fit program was applied to the spectra in order to extract each oxide contribution. The position of the fitted single absorption bands makes it possible to identify the different oxides. The oxide grown on {alpha}{sub 2}-TiAl phase, consists of {alpha}-Al{sub 2}O{sub 3} and rutile TiO{sub 2} (24 h to 500 h of oxidation treatment), {gamma}-Al{sub 2}O{sub 3} and rutile TiO{sub 2} for 1000 h of oxidation treatment. Chemical maps reveal heterogeneous distribution of the oxides in the layer. A detailed surface characterization showed that the surface was principally covered with {alpha}-Al{sub 2}O{sub 3} and locally with an Al{sub 2}O{sub 3}/TiO{sub 2} mixture. In the case of {gamma}-TiAl oxidation, the oxide film consists of {alpha}-Al{sub 2}O{sub 3}, {gamma}-Al{sub 2}O{sub 3} and

  7. Voltage-controlled magnetic anisotropy in Fe|MgO tunnel junctions studied by x-ray absorption spectroscopy

    Miwa, Shinji, E-mail: miwa@mp.es.osaka-u.ac.jp; Matsuda, Kensho; Tanaka, Kazuhito; Goto, Minori; Suzuki, Yoshishige [Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531 (Japan); Kotani, Yoshinori; Nakamura, Tetsuya [Japan Synchrotron Radiation Research Institute/SPring-8, Sayo, Hyogo 679-5198 (Japan)

    2015-10-19

    In this study, voltage-controlled magnetic anisotropy (VCMA) in Fe|MgO tunnel junctions was investigated via the magneto-optical Kerr effect, soft x-ray absorption spectroscopy, and magnetic circular dichroism spectroscopy. The Fe|MgO tunnel junctions showed enhanced perpendicular magnetic anisotropy under external negative voltage, which induced charge depletion at the Fe|MgO interface. Despite the application of voltages of opposite polarity, no trace of chemical reaction such as a redox reaction attributed to O{sup 2−} migration was detected in the x-ray absorption spectra of the Fe. The VCMA reported in the Fe|MgO-based magnetic tunnel junctions must therefore originate from phenomena associated with the purely electric effect, that is, surface electron doping and/or redistribution induced by an external electric field.

  8. Voltage-controlled magnetic anisotropy in Fe|MgO tunnel junctions studied by x-ray absorption spectroscopy

    In this study, voltage-controlled magnetic anisotropy (VCMA) in Fe|MgO tunnel junctions was investigated via the magneto-optical Kerr effect, soft x-ray absorption spectroscopy, and magnetic circular dichroism spectroscopy. The Fe|MgO tunnel junctions showed enhanced perpendicular magnetic anisotropy under external negative voltage, which induced charge depletion at the Fe|MgO interface. Despite the application of voltages of opposite polarity, no trace of chemical reaction such as a redox reaction attributed to O2− migration was detected in the x-ray absorption spectra of the Fe. The VCMA reported in the Fe|MgO-based magnetic tunnel junctions must therefore originate from phenomena associated with the purely electric effect, that is, surface electron doping and/or redistribution induced by an external electric field

  9. Characterization of green copper phase pigments in Egyptian artifacts with X-ray absorption spectroscopy and principal components analysis

    The characterization of materials in historical artifacts can contribute significantly to their preservation and understanding; however, sampling and characterization are ideally performed using non-destructive approaches. The analysis of green pigments from Egyptian artifacts presents a further challenge as responses to laboratory based techniques have proven unsuccessful in many cases. An alternative approach is the use of non-destructive X-ray absorption near-edge structure spectroscopy, which was performed on a reference set of copper-containing green minerals and other compounds. Data projection using principal component analysis was used to explore the spectral data structures and to illustrate the relationship between the spectra and copper speciation, resulting in a calibration or training set of the reference materials used. Data from the training set were compared with samples from Egyptian artifacts. The combination of X-ray absorption spectroscopy with principal components analysis provides a novel approach in archeometry and the characterization of objects of cultural heritage

  10. Direct correlation of charge transfer absorption with molecular donor:acceptor interfacial area via photothermal deflection spectroscopy

    Domingo, Ester

    2015-04-09

    We show that the Charge Transfer (CT) absorption signal in bulk-heterojunction (BHJ) solar cell blends, measured by photothermal deflection spectroscopy (PDS), is directly proportional to the density of molecular donor/acceptor interfaces. Since the optical transitions from ground state to the interfacial CT state are weakly allowed at photon energies below the optical gap of both donor and acceptor, we can exploit the use of this sensitive linear absorption spectroscopy for such quantification. Moreover, we determine the absolute molar extinction coefficient of the CT transition for an archetypical polymer-fullerene interface. The latter is ~100 times lower than the extinction coefficient of the donor chromophore involved, allowing us to experimentally estimate the transition dipole moment (0.3 D) and the electronic coupling between ground state and CT state to be on the order of 30 meV.

  11. Applications of atomic absorption spectroscopy towards the analysis of scalp hair diagnosing epilepsy

    In recent years a considerable effort has been directed at the measurement of trace metal levels in various human tissues with the view of correlating these trace metals to human health and disease Scalp hair has been suggested as a potentially valuable tissue in recording changes in the levels of many trace, elements in the body over a long period of time. Levels of fe, Cu, Zn, Cr, Mg and Ca are determined in scalp hair adult epileptic normal male and female subjects by atomic absorption spectroscopy. A total of 85 hair samples for normal male/female subjects and 78 of male/female epileptic subjects were analyzed within the respective age groups of 28 to 30 and 24 to 27 years. The study showed higher average concentration of Zn, Fe and Cu in normal male adults than those found in epileptic subjects. Epileptic females showed higher average concentrations of Zn, Ca and Cu. The correlation coefficient study indicated significant correlation (r>0.589 at p=0.001) between Fe and Cr, Mg. Ca and Cu for epileptic females only. For normal male subjects Ca showed a strong correlation for Zn and Fe and for Cr and Ca. The regression analysis showed the significant role of Zn, Ca, Mg and Cr in scalp hair of normal and epileptic subjects. Accordingly, the metal to metal ratio analysis revealed critical Mg/Zn ratios as indicators of healthy (1) subjects. The ratio date are used for evaluation of the status of epileptic patients based on their ailment history. (author)

  12. Cadmium Chemical Form in Mine Waste Materials by X-ray Absorption Spectroscopy

    This study examines the molecular form of cadmium (Cd) present in mine wastes by X-ray Absorption Spectroscopy (XAS; Cd>20 mg/kg) using the K-edge of Cd at the Photon Factory Advanced Ring (PF-AR), NW10A beam line at KEK-Tsukuba-Japan. Mine waste materials and zinc concentrate were analyzed for Cd by ICPMS prior to undertaking XAS (range 21-452 mg/kg). Model compounds (CdO, Cd(OH)2, CdCO3, Cdacetate, CdS, Cdstearate, CdDEDTC) and samples were examined in solid form at 20 K. The XANES spectra showed similar E max values for both model compounds and samples. The EXAFS showed that Cd-S in CdS, gives a flatter spectrum in the extended region compared to Cd-O found with CdCO3, CdO and Cd Stearate. Linear combination fitting with model Cd compounds did not give clear assignments of composition, indicating that more detailed EXAFS spectra is required as mineral forms containing Cd were present rather than simple Cd compounds such as CdCO3. The Cd bond for a single shell model in mine waste sample matrices appears to be either Cd-O or Cd-S, or a combination of both. Comparison of molecular data from the XAS studies with bioaccessibility data giving a prediction of bioavailability for mine waste materials provides useful information about the significance of the cadmium form as a contaminant for health risk assessment purposes.

  13. The use of (micro)-X-ray absorption spectroscopy in cement research

    Long-term predictions on the mobility and the fate of radionuclides and contaminants in cementitious waste repositories require a molecular-level understanding of the geochemical immobilization processes involved. In this study, the use of X-ray absorption spectroscopy (XAS) for chemical speciation of trace elements in cementitious materials will be outlined presenting two examples relevant for nuclear waste management. The first example addresses the use of XAS on powdered cementitious materials to determine the local coordination environment of Sn(IV) bound to calcium silicate hydrates (C-S-H). Sn K-edge XAS data of Sn(IV) doped C-S-H can be rationalized by corner sharing binding of Sn octahedra to Si tetrahedra of the C-S-H structure. XAS was further applied to determine the binding mechanism of Sn(IV) in the complex cement matrix. The second example illustrates the potential of emerging synchrotron-based X-ray micro-probe techniques for elucidating the spatial distribution and the speciation of contaminants in highly heterogeneous cementitious materials at the micro-scale. Micro X-ray fluorescence (XRF) and micro-XAS investigations were carried out on Co(II) doped hardened cement paste. These preliminary investigations reveal a highly heterogeneous spatial Co distribution. The presence of a Co(II)-hydroxide-like phase Co(OH)2 and/or Co-Al layered double hydroxide (Co-Al LDH) or Co-phyllosilicate was observed. Surprisingly, some of the initial Co(II) was partially oxidized and incorporated into a Co(III)O(OH)-like phase or a Co-phyllomanganate

  14. X-ray absorption spectroscopy of aqueous aluminum-organic complexes.

    Hay, Michael B; Myneni, Satish C B

    2010-05-27

    Aqueous-phase X-ray absorption near-edge structure (XANES) spectra were collected on dissolved Al complexes with organic ligands, including desferrioxamine B, EDTA, acetohydroxamate, malate, oxalate, and salicylate. Spectral interpretations were made using the density functional theory-based modeling package StoBe. The goals of this work were to study the geometric and electronic structural characteristics of these complexes relative to Al(H(2)O)(6)(3+) and to examine the utility of the aqueous Al XANES technique as a tool for probing Al speciation and structure. In the case of EDTA, aqueous Fourier-transform infrared spectroscopy was also used to corroborate the structures of the Al(EDTA)(-) and AlOH(EDTA)(2-) complexes. Synthetic XANES spectra calculated with StoBe reproduced the observed spectral differences between Al(H(2)O)(6)(3+), Al(dfoB)(+), and Al(EDTA)(-). The narrower XANES feature observed for Al(dfoB)(+) relative to Al(H(2)O)(6)(3+) can be attributed to a weaker splitting of the Al 3p-O 2p interactions in the former, while Al(EDTA)(-) exhibits split Al 3p-ligand interactions that likely result from the mixed O/N coordination. In complexes with mixed aqua/organic-oxygen ligation (Al-acetohydroxamate, Al-malate, Al-oxalate, and Al-salicylate), spectra exhibit linear, systematic changes in peak width as a function of H(2)O to organic ligand ratio in the Al coordination sphere. These results highlight the sensitivity of the aqueous Al K-edge XANES spectrum to coordination environment and demonstrate its utility as an experimental probe for future studies of Al speciation in complex solutions. PMID:20443586

  15. Application of tunable diode laser absorption spectroscopy in the detection of oxygen

    Zhou, Xin; Jin, Xing

    2015-10-01

    Most aircrafts is driven by chemic energy which is released in the combustion process. For improving the capability of engine and controlling the running on-time, the processes of fuel physics and chemistry need to be analysis by kinds of high quality sensor. In the research of designing and improving the processes of fuel physics and chemistry, the concentration, temperature and velocity of kinds of gas in the combustor need to be detected and measured. In addition, these engines and research equipments are always in the harsh environment of high temperature, high pressure and high speed. The harsh environment needs the sensor to be high reliability, well repetition, no cross- sensitivity between gases, and the traditional measurement system can't satisfy the metrical requirement well. Tunable diode laser absorption spectroscopy (TDLAS) analytic measurement technology can well satisfy the measurement in the harsh environment, which can support the whole measurement plan and high quality measurement system. Because the TDLAS sensor has the excellence of small bulk, light weight, high reliability and well specifically measurement, the TDLAS measurement technology has wide prospects. Different from most measurements, only a beam of laser can be pass through the measured environment by TDLAS, and the measurement equipment needn't be set in the harsh environment. So, the TDLAS equipment can't be interrupted by the measured equipment. The ability of subsistence in the harsh environment is very valuable, especially in the measurement on the subject of aerospace with environment of high speed, combustion and plasma. This paper focuses on the collecting the articles on the subject of oxygen detection of TDLAS. By analyzing the research and results of the articles, we conclude the central issues, difficulties and results. And we can get some instructive conclusions.

  16. Development of a portable active long-path differential optical absorption spectroscopy system for volcanic gas measurements

    Vita, F.; C. Kern; Inguaggiato, S

    2014-01-01

    Active long-path differential optical absorption spectroscopy (LP-DOAS) has been an effective tool for measuring atmospheric trace gases for several decades. However, instruments were large, heavy and power-inefficient, making their application to remote environments extremely challenging. Recent developments in fibre-coupling telescope technology and the availability of ultraviolet light emitting diodes (UV-LEDS) have now allowed us to design and construct a lightweight, po...

  17. Study of Charge, Spin and Orbital States in Novel Transition-Metal Oxides Using X-Ray Absorption Spectroscopy

    Burnus, Tobias

    2008-01-01

    Transition-metal compounds show a wealth of intriguing properties such as superconductivity, piezoelectricity, giant magnetoresistance, spin and metal-insulator transitions, which are governed by the interplay of charge, spin, and orbital degrees of freedom. The knowledge of their electronic structure is crucial for understanding and predicting the fascinating properties of these often strongly correlated materials. In this thesis x-ray absorption spectroscopy including x-ray magnetic circula...

  18. Retrieval of Atmospheric Aerosol and Trace Gas Vertical Profiles using Multi-Axis Differential Optical Absorption Spectroscopy

    Yilmaz, Selami

    2012-01-01

    In this thesis, the vertical distribution of atmospheric trace gases and aerosols were retrieved using Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS). Various inversion methods were used to retrieve the profiles from the MAX-DOAS measurements. A new MAX-DOAS instrument optimized for the measurement of aerosol and trace gas profiles was developed. The retrieval methods were tested and advanced in the scope of the EUSAAR (European Supersites for Atmospheric Aerosol Research)...

  19. Differential optical absorption spectroscopy (DOAS) and air mass factor concept for a multiply scattering vertically inhomogeneous medium: theoretical consideration

    Rozanov, V.V.; Rozanov, A.V.

    2010-01-01

    The Differential Optical Absorption Spectroscopy (DOAS) technique is widely used to retrieve amounts of atmospheric species from measurements of the direct solar light transmitted through the Earth's atmosphere as well as of the solar light scattered in the atmosphere or reflected from the Earth's surface. For the transmitted direct solar light the theoretical basis of the DOAS technique represented by the Beer-Lambert law is well studied. In contrast, scarcely investigated is the theoretical...

  20. Two instruments based on differential optical absorption spectroscopy (DOAS) to measure accurate ammonia concentrations in the atmosphere

    H. Volten; Bergwerff, J.B.; M. Haaima; Lolkema, D. E.; A. J. C. Berkhout; G. R. van der Hoff; C. J. M. Potma; R. J. Wichink Kruit; W. A. J. van Pul; D. P. J. Swart

    2011-01-01

    We present two Differential Optical Absorption Spectroscopy (DOAS) instruments built at RIVM: the RIVM DOAS and the miniDOAS. Both instruments provide virtually interference-free measurements of NH3 concentrations in the atmosphere, since they measure over an open path, without suffering from inlet problems or interference problems by ammonium aerosols dissociating on tubes or filters. They measure concentrations up to at least 200 μg m−3, have a ...

  1. Determination of the relative concentrations of rare earth ions by x-ray absorption spectroscopy: Application to terbium mixed oxides

    Laan, van der, Paul Maarten; Fuggle, J.C.; van Dijk; Burggraaf, A.J.; Esteva, J.-M.; Karnatak, R.

    1986-01-01

    A method, based on X-ray absorption spectroscopy (XAS) in the range 0.8–1.5 keV, to determine the relative amounts of rare earth ions in different valencies is explained and tested for the case of terbium mixed oxides. The results are in agreement with those obtained by existing analytical methods. The XAS method is advantageous in that it can be applied where other, conventional, methods break down.

  2. Chemical state of Ag in Conducting Bridge Random Access Memory cells: a depth resolved X-ray Absorption Spectroscopy investigation.

    d'Acapito, F.; Souchier, E.; Noe, P.; Blaise, P.; Bernard, M.; Jousseaume, V.

    2016-05-01

    Conducting Bridge Random Access Memories (CBRAM) are a promising substitute for FLASH technology but problems with limited retention of the low resistance ON state still hamper their massive deployment. Depth resolved X-ray Absorption Spectroscopy has been used to describe the chemical state of the atoms of the active electrode (in this case Ag) and to reveal the role of Sb as stabilizer of the metallic state.

  3. State of Ni in catalysts for glycerol hydrogenation and methane steam reforming as studied by X-ray absorption spectroscopy

    Tkachenko, O. P.; Kustov, L. M.

    2013-06-01

    X-ray absorption spectroscopy is used to study 1% Ni/Al2O3, 5% Ni/Al2O3, and 5% Ni/TiO2 catalysts for glycerol and methane conversion. The effect of treatment in H2 under microwave irradiation on the reduction of part of the nickel to the metallic state in the titanium oxide-supported catalyst is demonstrated.

  4. Structural study of thin films prepared from tungstate glass matrix by Raman and X-ray absorption spectroscopy

    Thin films were prepared using glass precursors obtained in the ternary system NaPO3-BaF2-WO3 and the binary system NaPO3-WO3 with high concentrations of WO3 (above 40% molar). Vitreous samples have been used as a target to prepare thin films. Such films were deposited using the electron beam evaporation method onto soda-lime glass substrates. Several structural characterizations were performed by Raman spectroscopy and X-ray Absorption Near Edge Spectroscopy (XANES) at the tungsten LI and LIII absorption edges. XANES investigations showed that tungsten atoms are only sixfold coordinated (octahedral WO6) and that these films are free of tungstate tetrahedral units (WO4). In addition, Raman spectroscopy allowed identifying a break in the linear phosphate chains as the amount of WO3 increases and the formation of P-O-W bonds in the films network indicating the intermediary behavior of WO6 octahedra in the film network. Based on XANES data, we suggested a new attribution of several Raman absorption bands which allowed identifying the presence of W-O- and W=O terminal bonds and a progressive apparition of W-O-W bridging bonds for the most WO3 concentrated samples (above 40% molar) attributed to the formation of WO6 clusters

  5. Local Structure Determination of Carbon/Nickel Ferrite Composite Nanofibers Probed by X-ray Absorption Spectroscopy.

    Nilmoung, Sukunya; Kidkhunthod, Pinit; Maensiri, Santi

    2015-11-01

    Carbon/NiFe2O4 composite nanofibers have been successfully prepared by electrospinning method using a various concentration solution of Ni and Fe nitrates dispersed into polyacrylonitride (PAN) solution in N,N' dimethylformamide. The phase and mophology of PAN/NiFe2O4 composite samples were characterized and investigated by X-ray diffraction and scanning electron microscopy. The magnetic properties of the prepared samples were measured at ambient temperature by a vibrating sample magnetometer. It is found that all composite samples exhibit ferromagnetism. This could be local-structurally explained by the existed oxidation states of Ni2+ and Fe3+ in the samples. Moreover, local environments around Ni and Fe ions could be revealed by X-ray absorption spectroscopy (XAS) measurement including X-ray absorption near edge structure (XANES) and Extended X-ray absorption fine structure (EXAFS). PMID:26726677

  6. Reconstruction of combustion temperature and gas concentration distributions using line-of-sight tunable diode laser absorption spectroscopy

    Zhang, Zhirong; Sun, Pengshuai; Pang, Tao; Xia, Hua; Cui, Xiaojuan; Li, Zhe; Han, Luo; Wu, Bian; Wang, Yu; Sigrist, Markus W.; Dong, Fengzhong

    2016-07-01

    Spatial temperature and gas concentration distributions are crucial for combustion studies to characterize the combustion position and to evaluate the combustion regime and the released heat quantity. Optical computer tomography (CT) enables the reconstruction of temperature and gas concentration fields in a flame on the basis of line-of-sight tunable diode laser absorption spectroscopy (LOS-TDLAS). A pair of H2O absorption lines at wavelengths 1395.51 and 1395.69 nm is selected. Temperature and H2O concentration distributions for a flat flame furnace are calculated by superimposing two absorption peaks with a discrete algebraic iterative algorithm and a mathematical fitting algorithm. By comparison, direct absorption spectroscopy measurements agree well with the thermocouple measurements and yield a good correlation. The CT reconstruction data of different air-to-fuel ratio combustion conditions (incomplete combustion and full combustion) and three different types of burners (one, two, and three flat flame furnaces) demonstrate that TDLAS has the potential of short response time and enables real-time temperature and gas concentration distribution measurements for combustion diagnosis.

  7. Observation of phycoerythrin-containing cyanobacteria and other phytoplankton groups from space using Differential Optical Absorption Spectroscopy on SCIAMACHY data

    Bracher, Astrid; Dinter, Tilman; Burrows, John P.; Vountas, Marco; Röttgers, Rüdiger; Peeken, Ilka

    In order to understand the marine phytoplankton's role in the global marine ecosystem and biogeochemical cycles it is necessary to derive global information on the distribution of major functional phytoplankton types (PFT) in the world oceans. In our study we use instead of the common ocean color sensors such as CZCS, SeaWiFS, MODIS, MERIS, with rather low spectral resolution, the Differential Optical Absorption Spectroscopy (DOAS) to study the retrieval of phytoplankton distribution and absorption with the satellite sensor Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY). SCIAMACHY measures back scattered solar radiation in the UV-Vis-NIR spectral region with a high spectral resolution (0.2 to 1.5 nm). We used in-situ measured phytoplankton absorption spectra from two different RV Polarstern expeditions where different phytoplankton groups were representing or dominating the phytoplankton composition in order to identify these characteristic absorption spectra in SCIAMACHY data in the range of 430 to 500 nm and also to identify absorption from cyanobacterial photosynthetic pigment phycoerythrin. Our results show clearly these absorptions in the SCIAMACHY data. The conversion of these differential absorptions by including the information of the light penetration depth (according to Vountas et al., Ocean Science, 2007) globally distributed pigment concentrations for these characteristic phytoplankton groups for two monthly periods (Feb-March 2004, Oct-Nov 2005 and Oct-Nov 2007) are derived. The satellite retrieved information on cyanobacteria (Synechococcus sp. and Prochlorococcus sp.) and diatoms distribution matches well with the concentration measured from collocated water samples with HPLC technique and also to global model analysis with the NASA Ocean Biogeochemical Model (NOBM from http://reason.gsfc.nasa.gov/OPS/Giovanni/) according to Gregg and Casey 2006 and Gregg 2006. Results are of great importance for global modelling of

  8. Tomographic multiaxis-differential optical absorption spectroscopy observations of Sun-illuminated targets: a technique providing well-defined absorption paths in the boundary layer.

    Frins, Erna; Bobrowski, Nicole; Platt, Ulrich; Wagner, Thomas

    2006-08-20

    A novel experimental procedure to measure the near-surface distribution of atmospheric trace gases by using passive multiaxis differential absorption optical spectroscopy (MAX-DOAS) is proposed. The procedure consists of pointing the receiving telescope of the spectrometer to nonreflecting surfaces or to bright targets placed at known distances from the measuring device, which are illuminated by sunlight. We show that the partial trace gas absorptions between the top of the atmosphere and the target can be easily removed from the measured total absorption. Thus it is possible to derive the average concentration of trace gases such as NO(2), HCHO, SO(2), H(2)O, Glyoxal, BrO, and others along the line of sight between the instrument and the target similar to the well-known long-path DOAS observations (but with much less expense). If tomographic arrangements are used, even two- or three-dimensional trace gas distributions can be retrieved. The basic assumptions of the proposed method are confirmed by test measurements taken across the city of Heidelberg. PMID:16892129

  9. An experimental set-up to apply polarization modulation to infrared reflection absorption spectroscopy for improved in situ studies of atmospheric corrosion processes

    Wiesinger, R. [Institute of Science and Technology in Art, Academy of Fine Arts, 1010 Vienna (Austria); Schade, U. [Helmholtz-Zentrum für Materialien und Energy GmbH, Elektronenspeicherring BESSY II, 12489 Berlin (Germany); Kleber, Ch. [Centre for Electrochemical Surface Technology, 2700 Wiener Neustadt (Austria); Schreiner, M. [Institute of Science and Technology in Art, Academy of Fine Arts, 1010 Vienna (Austria); Institute for Chemical Technologies and Analytics, Vienna University of Technology, 1060 Vienna (Austria)

    2014-06-15

    A new set-up for improved monitoring of atmospheric corrosion processes in situ and in real-time is presented. To characterize chemical structures of thin films on metal surfaces surface sensitive analytical techniques are required. One possible technique is Infrared Reflection Absorption Spectroscopy (IRRAS) which has become an established method to investigate surface corrosion films of thicknesses less than 200 nm. However, there are limitations related to the sensitivity of these measurements, in case of investigating ultrathin films or absorption bands of interest, surface species are superimposed by atmospheric background absorption, which changes during in situ measurements in ambient atmospheres. These difficulties of in situ surface reflection measurements can be eliminated by availing the polarization selectivity of adsorbed surface species. At grazing angles of incidence the absorption of p-polarized infrared radiation by thin surface films on metals is enhanced, while the absorption of s-polarized light by this film is nearly zero. This different behavior of the polarization properties leads to strong selection rules at the surface and can therefore be used to identify molecules adsorbed on metal surfaces. Polarization Modulation (PM) of the infrared (IR) light takes advantage of this disparity of polarization on sample surfaces and in combination with IRRAS yielding a very sensitive and surface-selective method for obtaining IR spectra of ultra-thin films on metal surfaces. An already existing in situ IRRAS/Quartz Crystal Microbalance weathering cell was combined with PM and evaluated according to its applicability to study in situ atmospheric corrosion processes. First real-time measurements on silver samples exposed to different atmospheres were performed showing the advantage of PM-IRRAS compared to conventional IRRAS for such investigations.

  10. An experimental set-up to apply polarization modulation to infrared reflection absorption spectroscopy for improved in situ studies of atmospheric corrosion processes

    Wiesinger, R.; Schade, U.; Kleber, Ch.; Schreiner, M.

    2014-06-01

    A new set-up for improved monitoring of atmospheric corrosion processes in situ and in real-time is presented. To characterize chemical structures of thin films on metal surfaces surface sensitive analytical techniques are required. One possible technique is Infrared Reflection Absorption Spectroscopy (IRRAS) which has become an established method to investigate surface corrosion films of thicknesses less than 200 nm. However, there are limitations related to the sensitivity of these measurements, in case of investigating ultrathin films or absorption bands of interest, surface species are superimposed by atmospheric background absorption, which changes during in situ measurements in ambient atmospheres. These difficulties of in situ surface reflection measurements can be eliminated by availing the polarization selectivity of adsorbed surface species. At grazing angles of incidence the absorption of p-polarized infrared radiation by thin surface films on metals is enhanced, while the absorption of s-polarized light by this film is nearly zero. This different behavior of the polarization properties leads to strong selection rules at the surface and can therefore be used to identify molecules adsorbed on metal surfaces. Polarization Modulation (PM) of the infrared (IR) light takes advantage of this disparity of polarization on sample surfaces and in combination with IRRAS yielding a very sensitive and surface-selective method for obtaining IR spectra of ultra-thin films on metal surfaces. An already existing in situ IRRAS/Quartz Crystal Microbalance weathering cell was combined with PM and evaluated according to its applicability to study in situ atmospheric corrosion processes. First real-time measurements on silver samples exposed to different atmospheres were performed showing the advantage of PM-IRRAS compared to conventional IRRAS for such investigations.

  11. An experimental set-up to apply polarization modulation to infrared reflection absorption spectroscopy for improved in situ studies of atmospheric corrosion processes

    A new set-up for improved monitoring of atmospheric corrosion processes in situ and in real-time is presented. To characterize chemical structures of thin films on metal surfaces surface sensitive analytical techniques are required. One possible technique is Infrared Reflection Absorption Spectroscopy (IRRAS) which has become an established method to investigate surface corrosion films of thicknesses less than 200 nm. However, there are limitations related to the sensitivity of these measurements, in case of investigating ultrathin films or absorption bands of interest, surface species are superimposed by atmospheric background absorption, which changes during in situ measurements in ambient atmospheres. These difficulties of in situ surface reflection measurements can be eliminated by availing the polarization selectivity of adsorbed surface species. At grazing angles of incidence the absorption of p-polarized infrared radiation by thin surface films on metals is enhanced, while the absorption of s-polarized light by this film is nearly zero. This different behavior of the polarization properties leads to strong selection rules at the surface and can therefore be used to identify molecules adsorbed on metal surfaces. Polarization Modulation (PM) of the infrared (IR) light takes advantage of this disparity of polarization on sample surfaces and in combination with IRRAS yielding a very sensitive and surface-selective method for obtaining IR spectra of ultra-thin films on metal surfaces. An already existing in situ IRRAS/Quartz Crystal Microbalance weathering cell was combined with PM and evaluated according to its applicability to study in situ atmospheric corrosion processes. First real-time measurements on silver samples exposed to different atmospheres were performed showing the advantage of PM-IRRAS compared to conventional IRRAS for such investigations

  12. Formation of host-guest complexes on gold surface investigated by surface-enhanced IR absorption spectroscopy

    Inokuchi, Yoshiya; Mizuuchi, Takahiro; Ebata, Takayuki; Ikeda, Toshiaki; Haino, Takeharu; Kimura, Tetsunari; Guo, Hao; Furutani, Yuji

    2014-01-01

    We apply surface-enhanced infrared absorption (SEIRA) spectroscopy to host-guest complexes in liquid phase to examine the structural change in the complex formation. Two thiol derivatives of 18-crown-6 (18C6) are chemisorbed on a gold surface, and aqueous solutions of MCl salts (M = Li, Na, K, Rb, and Cs) are put to form M+·18C6 complexes. Infrared spectra of these complexes in the 900-2000 cm-1 region are obtained by SEIRA spectroscopy. The observed IR spectra show noticeable peaks due to the complex formation, demonstrating that SEIRA spectroscopy will be a powerful method to investigate the structure of host-guest complexes in supramolecular chemistry.

  13. Vacuum-UV spectroscopy of interstellar ice analogs. I. Absorption cross-sections of polar-ice molecules

    Cruz-Diaz, G A; Chen, Y -J; Yih, T -S

    2014-01-01

    The VUV absorption cross sections of most molecular solids present in interstellar ice mantles with the exception of H2O, NH3, and CO2 have not been reported yet. Models of ice photoprocessing depend on the VUV absorption cross section of the ice to estimate the penetration depth and radiation dose, and in the past, gas phase cross section values were used as an approximation. We aim to estimate the VUV absorption cross section of molecular ice components. Pure ices composed of CO, H2O, CH3OH, NH3, or H2S were deposited at 8 K. The column density of the ice samples was measured in situ by infrared spectroscopy in transmittance. VUV spectra of the ice samples were collected in the 120-160 nm (10.33-7.74 eV) range using a commercial microwave-discharged hydrogen flow lamp. We provide VUV absorption cross sections of the reported molecular ices. Our results agree with those previously reported for H2O and NH3 ices. Vacuum-UV absorption cross section of CH3OH, CO, and H2S in solid phase are reported for the first...

  14. Spectral studies of ocean water with space-borne sensor SCIAMACHY using Differential Optical Absorption Spectroscopy (DOAS

    M. Vountas

    2007-09-01

    Full Text Available Methods enabling the retrieval of oceanic parameter from the space borne instrumentation Scanning Imaging Absorption Spectrometer for Atmospheric ChartographY (SCIAMACHY using Differential Optical Absorption Spectroscopy (DOAS are presented. SCIAMACHY onboard ENVISAT measures back scattered solar radiation at a spectral resolution (0.2 to 1.5 nm. The DOAS method was used for the first time to fit modelled Vibrational Raman Scattering (VRS in liquid water and in situ measured phytoplankton absorption reference spectra to optical depths measured by SCIAMACHY. Spectral structures of VRS and phytoplankton absorption were clearly found in these optical depths. Both fitting approaches lead to consistent results. DOAS fits correlate with estimates of chlorophyll concentrations: low fit factors for VRS retrievals correspond to large chlorophyll concentrations and vice versa; large fit factors for phytoplankton absorption correspond with high chlorophyll concentrations and vice versa. From these results a simple retrieval technique taking advantage of both measurements is shown. First maps of global chlorophyll concentrations were compared to the corresponding MODIS measurements with very promising results. In addition, results from this study will be used to improve atmospheric trace gas DOAS-retrievals from visible wavelengths by including these oceanographic signatures.

  15. Catalysts at work: From integral to spatially resolved X-ray absorption spectroscopy

    Grunwaldt, Jan-Dierk; Kimmerle, Bertram; Baiker, Alfons; Boye, Pit; Schroer, Christian G.; Glatzel, Pieter; Borca, Camelia N.; Beckmann, Felix; (TUD); (SLS); (IMR-GAC); (ETH Zurich); (ESRF); (TU Dresden)

    2009-09-25

    Spectroscopic studies on heterogeneous catalysts have mostly been done in an integral mode. However, in many cases spatial variations in catalyst structure can occur, e.g. during impregnation of pre-shaped particles, during reaction in a catalytic reactor, or in microstructured reactors as the present overview shows. Therefore, spatially resolved molecular information on a microscale is required for a comprehensive understanding of theses systems, partly in ex situ studies, partly under stationary reaction conditions and in some cases even under dynamic reaction conditions. Among the different available techniques, X-ray absorption spectroscopy (XAS) is a well-suited tool for this purpose as the different selected examples highlight. Two different techniques, scanning and full-field X-ray microscopy/tomography, are described and compared. At first, the tomographic structure of impregnated alumina pellets is presented using full-field transmission microtomography and compared to the results obtained with a scanning X-ray microbeam technique to analyse the catalyst bed inside a catalytic quartz glass reactor. On the other hand, by using XAS in scanning microtomography, the structure and the distribution of Cu(0), Cu(I), Cu(II) species in a Cu/ZnO catalyst loaded in a quartz capillary microreactor could be reconstructed quantitatively on a virtual section through the reactor. An illustrating example for spatially resolved XAS under reaction conditions is the partial oxidation of methane over noble metal-based catalysts. In order to obtain spectroscopic information on the spatial variation of the oxidation state of the catalyst inside the reactor XAS spectra were recorded by scanning with a micro-focussed beam along the catalyst bed. Alternatively, full-field transmission imaging was used to efficiently determine the distribution of the oxidation state of a catalyst inside a reactor under reaction conditions. The new technical approaches together with quantitative data

  16. X-ray absorption spectroscopy on high-temperature superconductors and related compounds

    The electronic structure of the cuprate high-temperature superconductors La2-xSrxCuO4+δ, Tl2Ba2CaCu2O8 and Tl2Ba2Ca2Cu3O10 has been investigated using polarization-dependent near-edge X-ray absorption fine structure spectroscopy (NEXAFS). In addition, La2-xSrxNiO4+δ has been included in the actual study as an isostructural analogue to the La2-xSrxCuO4+δ system. It appears that the electronic structure of these compounds corresponds to that of a p-type doped charge-transfer insulator including electron-electron interactions on the Cu(Ni) sites and a strong hybridization between Cu(Ni) and O atoms. It is concluded that the low-energy excitations in these compounds can be described on the basis of an effective one-band Mott-Hubbard model. The polarization-dependence of the above spectra gives evidence for the strong in-plane character of the intrinsic and the doped holes. The small amount and the doping-dependence of the out-of-plane character of these charge carriers rule out models for a microscopic mechanism of superconductivity based on a large amount of hole states in the corresponding Apex-O2pz/Cu3d3z2-r2 orbitals. On the other hand, the reduction of this anisotropy in the overdoped compounds together with similar findings in the macroscopic properties seems to indicate a detrimental influence of non-planar orbitals on the superconducting properties. The differences in the energetic ordering and atomic character of the states close to the Fermi level between the undoped compounds La2CuO4+δ, La2NiO4+δ, and NiO have been determined from the NEXAFS data. It is found that these differences can be explained by the different size of the tetragonal crystal field splitting EZ compared to that of the Hund's rule interaction JH in these systems. This gives evidence for the high-spin d8 ground state of the undoped nickelates (i.e. JH>EZ). It is suggested that the polarons in La2-xSrxNiO4+δ can be seen as non-classical objects on the length scale of a lattice constant

  17. Estimation of lead, cadmium and nickel content by means of Atomic Absorption Spectroscopy in dry fruit bodies of some macromycetes growing in Poland. II.

    Jan Grzybek

    2014-08-01

    Full Text Available The content of lead, cadmium, and nickel in dry fruit bodies of 34 species of macromyoetes collected in Poland from 72 natural babitats by means of Atomic Absorption Spectroscopy (AAS was estimated.

  18. Ultra-fast X-ray absorption spectroscopy for the study of matter in transient regime; Spectroscopie d'absorption ultra-rapide de rayonnement X pour l'etude de la matiere en regime transitoire

    Lecherbourg, L

    2007-12-15

    In this work, we study the physics of dense matter, plasmas or solids, using X-ray absorption spectroscopy. Through the use of sources produced by laser-matter interaction, we have measured the absorption spectra of aluminum and bromine plasmas, as well as those of vanadium dioxide (VO{sub 2}). The measurement of absorption coefficients allows us to probe the dense matter and to study its properties. The experiments are carried out following the same principle: they use the same experimental set-up, called pump-probe. When the matter is dense, the absorption properties of an atom are modified by the surrounding environment. In a plasma, it is mainly the bound- bound transitions which are altered: the shapes of those spectral rays are modified. In a solid, the position of the neighbouring atoms in relation to the absorbing atom modify the structure of absorption levels (bound-free transition). The study of this structure allows us to measure the parameters of the material, and provides information such as the state of the electronic band or the interatomic gaps. The experiments carried out at the LULI have allowed us to probe plasmas in the relatively unknown regime of the Warm Dense Matter. One of the key parameters is that the plasma is characterised independently (FDI diagnostic). It allows for a better comparison of the measured absorption against a calculation made with the numerical model OPA-S. The experiments carried out at INRS have led to the realisation of an experimental system having the characteristics which allow the study of the dynamics of solids showing ultra-fast phase transition. For those experiments, we have used vanadium dioxide as a model system allowing us to test the feasibility of the method. (author)

  19. Gas cell based on optical contacting for fundamental spectroscopy studies with initial reference absorption spectrum of H2O vapor at 1723 K and 0.0235 bar

    Melin, Scott T.; Sanders, Scott T.

    2016-09-01

    A gas cell, using optically contacted sapphire windows to form a hot vapor seal, has been created for high temperature fundamental spectroscopy studies. It is designed to operate at temperatures from 280-2273 K and pressures from vacuum to 1.3 bar. Using the cell in conjunction with an external cavity diode laser spectrometer, a reference H2O vapor absorption spectrum at P=0.0235±0.0036 bar and T=1723±6 K was measured with 0.0001 cm-1 resolution over the 7326-7598 cm-1 range. Comparison of the measured spectrum to simulations reveals errors in both the HITEMP and BT2 databases. This work establishes heated static cell capabilities at temperatures well above the typical limit of approximately 1300 K set by quartz material properties. This paper addresses the design of the cell as well as the cell's limitations.

  20. Adsorption of cytochrome c to silica surfaces studied using evanescent wave broadband cavity-enhanced absorption spectroscopy

    Moore, L. J.; van der Sneppen, L.; Peverall, R.; Hancock, G.; Ritchie, G. A. D.

    2010-08-01

    The adsorption of cytochrome c (cyt c) to a silica surface has been studied by use of evanescent wave broadband cavityenhanced absorption spectroscopy (EW-BBCEAS). Visible radiation from a supercontinuum source is coupled into an optical cavity consisting of a pair of broadband high reflectivity mirrors, and a total internal reflection (TIR) event at the prism/water interface. Aqueous solutions of cyt c are placed onto the TIR footprint on the prism surface and the subsequent protein adsorption is probed by the resulting evanescent wave. The time integrated cavity output is directed into a spectrometer, where it is dispersed and analysed. The high spectral brilliance of the SC affords a baseline noise comparable to evanescent wave cavity ring-down spectroscopy (EW-CRDS), and the broadband nature of the source allows observation of a wide spectral range (ca 250 nm in the visible). The system is calibrated by measuring the absorption spectra of dyes of a known absorbance. Absorption spectra of cyt c are obtained for both S and P polarized radiation, allowing information about the orientation of the adsorbed protein to be extracted.

  1. Quantum cascade laser absorption sensor for carbon monoxide in high-pressure gases using wavelength modulation spectroscopy.

    Spearrin, R M; Goldenstein, C S; Jeffries, J B; Hanson, R K

    2014-03-20

    A tunable quantum cascade laser sensor, based on wavelength modulation absorption spectroscopy near 4.8 μm, was developed to measure CO concentration in harsh, high-pressure combustion gases. The sensor employs a normalized second harmonic detection technique (WMS-2f/1f) at a modulation frequency of 50 kHz. Wavelength selection at 2059.91  cm⁻¹ targets the P(20) transition within the fundamental vibrational band of CO, chosen for absorption strength and relative isolation from infrared water and carbon dioxide absorption. The CO spectral model is defined by the Voigt line-shape function, and key line-strength and line-broadening spectroscopic parameters were taken from the literature or measured. Sensitivity analysis identified the CO-N₂ collisional broadening coefficient as most critical for uncertainty mitigation in hydrocarbon/air combustion exhaust measurements, and this parameter was experimentally derived over a range of combustion temperatures (1100-2600 K) produced in a shock tube. Accuracy of the wavelength-modulation-spectroscopy-based sensor, using the refined spectral model, was validated at pressures greater than 40 atm in nonreactive shock-heated gas mixtures. The laser was then free-space coupled to an indium-fluoride single-mode fiber for remote light delivery. The fiber-coupled sensor was demonstrated on an ethylene/air pulse detonation combustor, providing time-resolved (~20  kHz), in situ measurements of CO concentration in a harsh flow field. PMID:24663473

  2. Absorption spectroscopy of cold caesium atoms confined in a magneto-optical trap

    Yan Shu-Bin; Liu Tao; Geng Tao; Zhang Tian-Cai; Peng Kun-Chi; Wang Jun-Min

    2004-01-01

    Absorption spectra of cold caesium atoms confined in a magneto-optical trap are measured around D2 line at 852nm with a weak probe beam. Absorption reduction dip due to electromagnetically induced transparency (EIT)effect induced by the cooling/trapping field in a V-type three-level system and a gain peak near the cycling transition are clearly observed. Several mechanisms mixed with EIT effect in a normal V-type three-level system are briefly discussed. A simple theoretical analysis based on a dressed-state model is presented for interpretation of the absorption spectra.

  3. Optical and structural properties of plasma-treated Cordyceps bassiana spores as studied by circular dichroism, absorption, and fluorescence spectroscopy

    Lee, Geon Joon; Sim, Geon Bo; Choi, Eun Ha; Kwon, Young-Wan; Kim, Jun Young; Jang, Siun; Kim, Seong Hwan

    2015-01-01

    To understand the killing mechanism of fungal spores by plasma treatment, the optical, structural, and biological properties of the insect pathogenic fungus Cordyceps bassiana spores were studied. A nonthermal atmospheric-pressure plasma jet (APPJ) was used to treat the spores in aqueous solution. Optical emission spectra of the APPJ acquired in air indicated emission peaks corresponding to hydroxyl radicals and atomic oxygen. When the APPJ entered the aqueous solution, additional reactive species were derived from the interaction of plasma radicals with the aqueous solution. Fluorescence and absorption spectroscopy confirmed the generation of hydroxyl radicals and hydrogen peroxide in the plasma-activated water (PAW). Spore counting showed that plasma treatment significantly reduced spore viability. Absorption spectroscopy, circular dichroism (CD) spectroscopy, and agarose gel electrophoresis of the DNA extracted from plasma-treated spores showed a reduction in spore DNA content. The magnitude of the dip in the CD spectrum was lower in the plasma-treated spores than in the control, indicating that plasma treatment causes structural modifications and/or damage to cellular components. Tryptophan fluorescence intensity was lower in the plasma-treated spores than in the control, suggesting that plasma treatment modified cell wall proteins. Changes in spore viability and DNA content were attributed to structural modification of the cell wall by reactive species coming from the APPJ and the PAW. Our results provided evidence that the plasma radicals and the derived reactive species play critical roles in fungal spore inactivation.

  4. Optical and structural properties of plasma-treated Cordyceps bassiana spores as studied by circular dichroism, absorption, and fluorescence spectroscopy

    Lee, Geon Joon, E-mail: gjlee@kw.ac.kr; Sim, Geon Bo; Choi, Eun Ha [Plasma Bioscience Research Center/Department of Electrical and Biological Physics, Kwangwoon University, Seoul 139-701 (Korea, Republic of); Kwon, Young-Wan [KU-KIST Graduate School of Converging Science and Technology, Korea University, Seoul 136-701 (Korea, Republic of); Kim, Jun Young; Jang, Siun; Kim, Seong Hwan, E-mail: piceae@naver.com [Department of Microbiology and Institute of Basic Sciences, Dankook University, Cheonan 330-714 (Korea, Republic of)

    2015-01-14

    To understand the killing mechanism of fungal spores by plasma treatment, the optical, structural, and biological properties of the insect pathogenic fungus Cordyceps bassiana spores were studied. A nonthermal atmospheric-pressure plasma jet (APPJ) was used to treat the spores in aqueous solution. Optical emission spectra of the APPJ acquired in air indicated emission peaks corresponding to hydroxyl radicals and atomic oxygen. When the APPJ entered the aqueous solution, additional reactive species were derived from the interaction of plasma radicals with the aqueous solution. Fluorescence and absorption spectroscopy confirmed the generation of hydroxyl radicals and hydrogen peroxide in the plasma-activated water (PAW). Spore counting showed that plasma treatment significantly reduced spore viability. Absorption spectroscopy, circular dichroism (CD) spectroscopy, and agarose gel electrophoresis of the DNA extracted from plasma-treated spores showed a reduction in spore DNA content. The magnitude of the dip in the CD spectrum was lower in the plasma-treated spores than in the control, indicating that plasma treatment causes structural modifications and/or damage to cellular components. Tryptophan fluorescence intensity was lower in the plasma-treated spores than in the control, suggesting that plasma treatment modified cell wall proteins. Changes in spore viability and DNA content were attributed to structural modification of the cell wall by reactive species coming from the APPJ and the PAW. Our results provided evidence that the plasma radicals and the derived reactive species play critical roles in fungal spore inactivation.

  5. [Research on the NO2 mean concentration measurement with target differential optical absorption spectroscopy technology].

    Liu, Jin; Si, Fu-Qi; Zhou, Hai-Jin; Zhao, Min-Jie; Dou, Ke; Liu, Wen-Qing

    2013-04-01

    A new monitoring method of NO2 concentration near ground with the target difference absorption spectrum technology (Target DOAS) is introduced in the present paper. This method is based on the passive difference absorption spectrum technology. The instrument collects solar reflection spectrum of remote objectives, such as wall of building and mountain, and a specific reference spectrum is chosen to subtract the influence of trace gases from the target to atmospheric top, then integrated concentration of NO2 along the path between the target and instrument can be calculated through the differential absorption spectra inversion algorithm. Since the distance between the instrument and target is given, the mean concentration of NO2 can be derived. With developed Target DOAS instrument, NO2 concentration measurement was carried out in Hefei. And comparison was made between the target DOAS and long path difference absorption spectrometer. Good consistency was presented, proving the feasibility of this method. PMID:23841393

  6. Actinides in molecules: exotic properties probed by X-ray Absorption Spectroscopy

    Den Auwer, C.; Moisy, P.; Guilbaud, P.; Guillaumont, D.; Simoni, E.; Conradson, S.D

    2004-07-01

    Dealing with actinide elements in molecular chemistry may result in particularly attractive and exotic physico-chemical properties. In solution, one of the spectroscopic tools able to selectively probe the structural or electronic properties of these molecules is the X-ray absorption process. Different aspects of absorption edge or EXAFS analysis related to actinide studies are presented, including phenomenological and semi-quantitative approaches. (authors)

  7. Actinides in molecules: exotic properties probed by X-ray Absorption Spectroscopy

    Dealing with actinide elements in molecular chemistry may result in particularly attractive and exotic physico-chemical properties. In solution, one of the spectroscopic tools able to selectively probe the structural or electronic properties of these molecules is the X-ray absorption process. Different aspects of absorption edge or EXAFS analysis related to actinide studies are presented, including phenomenological and semi-quantitative approaches. (authors)

  8. High energy resolution five-crystal spectrometer for high quality fluorescence and absorption measurements on an x-ray absorption spectroscopy beamline

    Fluorescence detection is classically achieved with a solid state detector (SSD) on x-ray absorption spectroscopy (XAS) beamlines. This kind of detection however presents some limitations related to the limited energy resolution and saturation. Crystal analyzer spectrometers (CAS) based on a Johann-type geometry have been developed to overcome these limitations. We have tested and installed such a system on the BM30B/CRG-FAME XAS beamline at the ESRF dedicated to the structural investigation of very dilute systems in environmental, material and biological sciences. The spectrometer has been designed to be a mobile device for easy integration in multi-purpose hard x-ray synchrotron beamlines or even with a laboratory x-ray source. The CAS allows to collect x-ray photons from a large solid angle with five spherically bent crystals. It will cover a large energy range allowing to probe fluorescence lines characteristic of all the elements from Ca (Z = 20) to U (Z = 92). It provides an energy resolution of 1–2 eV. XAS spectroscopy is the main application of this device even if other spectroscopic techniques (RIXS, XES, XRS, etc.) can be also achieved with it. The performances of the CAS are illustrated by two experiments that are difficult or impossible to perform with SSD and the complementarity of the CAS vs SSD detectors is discussed.

  9. Vacuum-UV spectroscopy of interstellar ice analogs. II. Absorption cross-sections of nonpolar ice molecules

    Cruz-Diaz, G A; Chen, Y -J; Yih, T -S

    2014-01-01

    Dust grains in cold circumstellar regions and dark-cloud interiors at 10-20 K are covered by ice mantles. A nonthermal desorption mechanism is invoked to explain the presence of gas-phase molecules in these environments, such as the photodesorption induced by irradiation of ice due to secondary ultraviolet photons. To quantify the effects of ice photoprocessing, an estimate of the photon absorption in ice mantles is required. In a recent work, we reported the vacuum-ultraviolet (VUV) absorption cross sections of nonpolar molecules in the solid phase. The aim was to estimate the VUV-absorption cross sections of nonpolar molecular ice components, including CH4, CO2, N2, and O2. The column densities of the ice samples deposited at 8 K were measured in situ by infrared spectroscopy in transmittance. VUV spectra of the ice samples were collected in the 120-160 nm (10.33-7.74 eV) range using a commercial microwave-discharged hydrogen flow lamp. We found that, as expected, solid N2 has the lowest VUV-absorption cros...

  10. Challenges for energy dispersive X-ray absorption spectroscopy at the ESRF: microsecond time resolution and Mega-bar pressures

    This Thesis concerns the development of two different applications of energy-dispersive X-ray absorption spectroscopy at the ESRF: time-resolved studies pushed to the microsecond time resolution and high-pressure studies at the limit of the Mega-bar pressures. The work has been developed in two distinct parts, and the underlying theme has been the exploitation of the capabilities of an X-ray absorption spectrometer in dispersive geometry on a third generation synchrotron source. For time-resolved studies, the study of the triplet excited state following a laser excitation of Pt2(P2O5H2)44- has been chosen to push the technique to the microsecond time resolution. In the high-pressure part, the suitability of the energy dispersive X-ray absorption spectrometer for high-pressure studies using diamond anvils cell is stressed. Some technical developments carried out on beamline ID24 are discussed. Finally, the most extensive scientific part concerns a combined X-ray absorption and diffraction study of InAs under pressure. (author)

  11. Satellite monitoring of different vegetation types by differential optical absorption spectroscopy (DOAS in the red spectral range

    T. Wagner

    2007-01-01

    Full Text Available A new method for the satellite remote sensing of different types of vegetation and ocean colour is presented. In contrast to existing algorithms relying on the strong change of the reflectivity in the red and near infrared spectral region, our method analyses weak narrow-band (few nm reflectance structures (i.e. "fingerprint" structures of vegetation in the red spectral range. It is based on differential optical absorption spectroscopy (DOAS, which is usually applied for the analysis of atmospheric trace gas absorptions. Since the spectra of atmospheric absorption and vegetation reflectance are simultaneously included in the analysis, the effects of atmospheric absorptions are automatically corrected (in contrast to other algorithms. The inclusion of the vegetation spectra also significantly improves the results of the trace gas retrieval. The global maps of the results illustrate the seasonal cycles of different vegetation types. In addition to the vegetation distribution on land, they also show patterns of biological activity in the oceans. Our results indicate that improved sets of vegetation spectra might lead to more accurate and more specific identification of vegetation type in the future.

  12. Experimental and theoretical study of electronic structure of aluminum in extreme conditions with X-ray absorption spectroscopy

    Matter in extreme conditions belongs to Warm Dense Matter regime which lays between dense plasma regime and condensed matter. This regime is still not well known, indeed it is very complex to generate such plasma in the laboratory to get experimental data and validate models. The goal of this thesis is to study electronic structure of aluminum in extreme conditions with X-ray absorption spectroscopy. Experimentally aluminum has reached high densities and high temperatures, up to now unexplored. An X-ray source has also been generated to probe highly compressed aluminum. Two spectrometers have recorded aluminum absorption spectra and aluminum density and temperature conditions have been deduced thanks to optical diagnostics. Experimental spectra have been compared to ab initio spectra, calculated in the same conditions. The theoretical goal was to validate the calculation method in high densities and high temperatures regime with the study of K-edge absorption modifications. We also used absorption spectra to study the metal-non metal transition which takes place at low density (density ≤ solid density). This transition could be study with electronic structure modifications of the system. (author)

  13. Microsecond X-ray Absorption Spectroscopy Identification of Co(I) Intermediates in Cobaloxime-Catalyzed Hydrogen Evolution.

    Smolentsev, Grigory; Cecconi, Bianca; Guda, Alexander; Chavarot-Kerlidou, Murielle; van Bokhoven, Jeroen A; Nachtegaal, Maarten; Artero, Vincent

    2015-10-19

    Rational development of efficient photocatalytic systems for hydrogen production requires understanding the catalytic mechanism and detailed information about the structure of intermediates in the catalytic cycle. We demonstrate how time-resolved X-ray absorption spectroscopy in the microsecond time range can be used to identify such intermediates and to determine their local geometric structure. This method was used to obtain the solution structure of the Co(I) intermediate of cobaloxime, which is a non-noble metal catalyst for solar hydrogen production from water. Distances between cobalt and the nearest ligands including two solvent molecules and displacement of the cobalt atom out of plane formed by the planar ligands have been determined. Combining in situ X-ray absorption and UV/Vis data, we demonstrate how slight modification of the catalyst structure can lead to the formation of a catalytically inactive Co(I) state under similar conditions. Possible deactivation mechanisms are discussed. PMID:26388205

  14. Sub-Doppler direct infrared laser absorption spectroscopy in fast ion beams: The fluorine hyperfine structure of HF +

    Coe, J. V.; Owrutsky, J. C.; Keim, E. R.; Agman, N. V.; Hovde, D. C.; Saykally, R. J.

    1989-04-01

    We report the development of a new general technique for measuring vibration-rotation spectra of molecular ions with sub-Doppler resolution and with accurate determination of the mass and number density of the carriers of all spectral features. With this method, called direct laser absorption spectroscopy in fast ion beams (DLASFIB), we have carried out the first observation of direct absorption of photons by ions in a fast ion beam. Hyperfine-resolved vibration-rotation transitions of HF+ have been measured, and along with optical combination differences and laser magnetic resonance data, have been analyzed to yield the fluorine hyperfine parameters a, b, c and d for both v=0 and v=1 in the X 2Π state. Comparisons with many-body perturbation theory results are presented.

  15. Sub-Doppler direct infrared laser absorption spectroscopy in fast ion beams: The fluorine hyperfine structure of HF/sup +/

    Coe, J.V.; Owrutsky, J.C.; Keim, E.R.; Agman, N.V.; Hovde, D.C.; Saykally, R.J.

    1989-04-15

    We report the development of a new general technique for measuring vibration--rotation spectra of molecular ions with sub-Doppler resolution and with accurate determination of the mass and number density of the carriers of all spectral features. With this method, called direct laser absorption spectroscopy in fast ion beams (DLASFIB), we have carried out the first observation of direct absorption of photons by ions in a fast ion beam. Hyperfine-resolved vibration--rotation transitions of HF/sup +/ have been measured, and along with optical combination differences and laser magnetic resonance data, have been analyzed to yield the fluorine hyperfine parameters a, b, c and d for both v = 0 and v = 1 in the X /sup 2/Pi state. Comparisons with many-body perturbation theory results are presented.

  16. Sub-Doppler direct infrared laser absorption spectroscopy in fast ion beams: The fluorine hyperfine structure of HF+

    We report the development of a new general technique for measuring vibration--rotation spectra of molecular ions with sub-Doppler resolution and with accurate determination of the mass and number density of the carriers of all spectral features. With this method, called direct laser absorption spectroscopy in fast ion beams (DLASFIB), we have carried out the first observation of direct absorption of photons by ions in a fast ion beam. Hyperfine-resolved vibration--rotation transitions of HF+ have been measured, and along with optical combination differences and laser magnetic resonance data, have been analyzed to yield the fluorine hyperfine parameters a, b, c and d for both v = 0 and v = 1 in the X 2Pi state. Comparisons with many-body perturbation theory results are presented

  17. Local versus global electronic properties of chalcopyrite alloys: X-ray absorption spectroscopy and ab initio calculations

    Element-specific unoccupied electronic states of Cu(In, Ga)S2 were studied as a function of the In/Ga ratio by combining X-ray absorption spectroscopy with density functional theory calculations. The S absorption edge shifts with changing In/Ga ratio as expected from the variation of the band gap. In contrast, the cation edge positions are largely independent of composition despite the changing band gap. This unexpected behavior is well reproduced by our calculations and originates from the dependence of the electronic states on the local atomic environment. The changing band gap arises from a changing spatial average of these localized states with changing alloy composition

  18. [The retrieval of ozone column densities by passive differential optical absorption spectroscopy during summer at Zhongshan Station, Antarctic].

    Luo, Yu-Han; Liu, Wen-Qing; Bian, Lin-Gen; Lu, Chang-Gui; Xie, Pin-Hua; Si, Fu-Qi; Sun, Li-Guang

    2011-02-01

    Daily ozone column densities were monitored by Passive DOAS (differential optical absorption spectroscopy) from December 10th, 2008 to Feb 19th, 2009 at Zhongshan Station, Antarctic (69 degrees 22'24" S, 76 degrees 22'14" E). Considering the absorption of O3, OClO, NO2, O4, BrO and the Ring effect, ozone slant column densities were retrieved using the zenith scattered sunlight as the light source. The results showed that there was no obvious "ozone hole" during the monitoring period, but ozone VCD (vertical column density) had greatly changed within short time scale, especially in middle December and early February. The analysis of passive DOAS and Brewer measurements of ozone VCD showed good agreement with the correlative coefficient of 0.863, while satellite board OMI measurements with the correlative coefficient of 0.840, which confirmed the validity of the monitoring of Passive DOAS. PMID:21510403

  19. Compact optical cell system for vacuum ultraviolet absorption and circular dichroism spectroscopy and its application to aqueous solution sample.

    Tanaka, Masahito; Yagi-Watanabe, Kazutoshi; Kaneko, Fusae; Nakagawa, Kazumichi

    2008-09-01

    We have designed a compact optical cell for studying the absorption and circular dichroism (CD) of a solution sample in the vacuum ultraviolet (VUV) region using a temperature control unit. The cell size was 34 mm in diameter and 14 mm in length. Such compactness was obtained by coating the VUV scintillator onto the outside of the back window. Because this scintillator converts the transmitted VUV light to visible light, the outside of this cell is operated under atmospheric pressure. The temperature of the sample solution was maintained in the range of 5 degrees C to 80 degrees C using a temperature control unit with a Peltier thermoelectric element. Changes in the sample temperature were observed by monitoring the absorption intensity of water. Through the study of VUV-CD spectra of ammonium camphor-10-sulfonate aqueous solutions and the transmitted spectrum of an empty cell, it was concluded that this cell unit has sufficient performance for use in VUV spectroscopy. PMID:18473342

  20. Line-Parameter Measurements and Stringent Tests of Line-Shape Models Based on Cavity-Enhanced Absorption Spectroscopy

    Bielska, Katarzyna; Fleisher, Adam J.; Hodges, Joseph T.; Lin, Hong; Long, David A.; Reed, Zachary D.; Sironneau, Vincent; Truong, Gar-Wing; Wójtewicz, Szymon

    2014-06-01

    Laser methods that are based on cavity-enhanced absorption spectroscopy (CEAS) are well-suited for measuring molecular line parameters under conditions of low optical density, and as such they are complementary to broadband Fourier-transform spectroscopy (FTS) techniques. Attributes of CEAS include relatively low detection limits, accurate and precise detuning axes and high fidelity measurements of line shape. In many cases these performance criteria are superior to those obtained using direct laser absorption spectroscopy and FTS-based systems. In this presentation we will survey several examples of frequency-stabilized cavity ring-down spectroscopy (FS-CRDS)1 measurements obtained with laser spectrometers developed at the National Institute of Standards and Technology (NIST) in Gaithersburg Maryland. These experiments, which are motivated by atmospheric monitoring and remote-sensing applications that require high-precision and accuracy, involve nearinfrared transitions of carbon dioxide, water, oxygen and methane. We discuss spectra with signal-to-noise ratios exceeding 106, frequency axes with absolute uncertainties in the 10 kHz to 100 kHz range and linked to a Cs clock, line parameters with relative uncertainties at the 0.2 % level and isotopic ratios measured with a precision of 0.03 %. We also present FS-CRDS measurements of CO2 line intensities which are measured at atmospheric concentration levels and linked to gravimetric standards for CO2 in air, and we quantify pressure-dependent deviations between various theoretical line profiles and measured line shapes. Finally we also present recent efforts to increase data throughput and spectral coverage in CEAS experiments. We describe three new high-bandwidth CEAS techniques including frequency-agile, rapid scanning spectroscopy (FARS)2, which enables continuous-wave measurements of cavity mode linewidth and acquisition of ringdown decays with no dead time during laser frequency tuning, heterodyne

  1. A Scanning Multi-Axis Differential Optical Absorption Spectroscopy System for Measurement of Tropospheric NO2 in Beijing

    LI Ang; XIE Pin-Hua; LIU Cheng; LIU Jian-Guo; LIU Wen-Qing

    2007-01-01

    A scanning multi-axis differential optical absorption spectroscopy (DOAS) system is developed for monitoring tropospheric NO2 abundance. Measurements at different viewing angles near the horizon can be performed sequentially with one telescope collecting scattered sunlight reflected by a moving mirror. Tropospheric NO2 diurnal variations can be derived from slant column densities (SCDs) of different elevation angles. The result from a field campaign in Beijing in summer of 2005 reveals potential possibility for the monitoring of tropospheric NO2 by multi-axis DOAS technique.

  2. Structural study on Si O2 porous gels doped with copper ny using x-ray absorption spectroscopy

    Si O2 porous matrix were prepared by sol-gel method and doped with copper adding Cu Cl and Cu SO4. The samples were prepared in monolithic shape, were dried at 1100 deg C. The structural evolution of these gels was studied by X-ray Absorption Spectroscopy (EXAFs and Xanes). The obtained spectra show the formation of Cu O phase in the samples prepared from Cu Cl and treated at 900 and 1100 deg C. In the samples prepared from Cu SO4 occur the formation of Cu O at 900 deg C and Cu2 O at 1100 deg C. (author)

  3. Evaluation of emery dust on the manufacture of abrasives by neutron activation analysis and atomic absorption spectroscopy

    In this work it is presented an evaluation on the degree of contamination by emery dust in a working area where abrasives are manufactured, in a factory located in the industrial area of Toluca City by neutron activation analysis and atomic absorption spectroscopy. The samples were collected on Whatman filters and attacked with hot concentrated HCl. The elements founded were: Al, Si, V, Mg, Br, Mn, Ni, Zn, Fe, Cr, Ca and Pb. They are a risk for the health of the workers. (Author)

  4. Determination of Hg(II) as a pollutant in Karachi coastal waters by cold vapor atomic absorption spectroscopy

    Now a days, environmental monitoring has great importance and mercury is well known for its toxicity. Mercury (which is at trace level) is analyzed by cold vapor atomic absorption spectroscopy with amendments that are appropriate to the present laboratory need. The results are consistent with previous analysis, through other methods, two areas namely Ibrahim Hyderi and Fisheries were found to have mercury levels around 0.193 mu/L and 0.110 mu g/L, respectively. Whereas other areas have mercury levels similar to other places reported earlier. (author)

  5. X-ray absorption spectroscopy and atomic force microscopy study of bias-enhanced nucleation of diamond films

    Garcia, M.M.; Jimenez, I.; Vazquez, L.; Gomez-Aleixandre, C.; Albella, J.M.; Sanchez, O. [Instituto de Ciencia de Materiales, C.S.I.C., Cantoblanco28049, Madrid (Spain); Terminello, L.J. [Lawrence Livermore National Laboratory, Livermore, California94551 (United States); Himpsel, F.J. [Department of Physics, University of Wisconsin--Madison, Madison, Wisconsin53706 (United States)

    1998-04-01

    The bias-enhanced nucleation of diamond on Si(100) has been studied by x-ray absorption near-edge spectroscopy (XANES) and atomic force microscopy, two techniques well suited to characterize nanometric crystallites. Diamond nuclei of {approximately}15nm are formed after 5 min of bias-enhanced treatment. The number of nuclei and its size increases with the time of application of the bias voltage. A nanocrystalline diamond film is attained after 20 min of bias-enhanced nucleation. At the initial nucleation stages, the Si substrate appears covered with diamond crystallites and graphite, without SiC being detected by XANES. {copyright} {ital 1998 American Institute of Physics.}

  6. A flow-through x-ray absorption spectroscopy cell for characterization of powder catalysts in the working state

    Odzak, J. F.; Argo, A. M.; Lai, F. S.; Gates, B. C.; Pandya, K.; Feraria, L.

    2001-10-01

    We report the design and demonstration of an x-ray absorption spectroscopy (XAS) cell used for the characterization of solid (powder) catalysts in operation with gas-phase reactants. The use of powder samples removes complications arising from mass transfer limitations in pressed wafer samples, the typical form of catalyst used in other in situ XAS cells. The new cell allows collection of XAS data at temperatures ranging from about 230 to 470 K, gas flow rates ranging from about 10 to 500 ml min-1, and pressures ranging from about 1 to 3 atm. The cell is designed to function nearly as a plug flow reactor.

  7. Fiber-distributed multi-channel open-path H2S sensor based on tunable diode laser absorption spectroscopy

    Dong Chen; Wenqing Liu; Yujun Zhang; Jianguo Liu; Ruifeng Kan; Min Wang; Xi Fang; Yiben Cui

    2007-01-01

    Tunable diode laser based gas detectors are now being used in a wide variety of applications for safety and environmental interest. A fiber-distributed multi-channel open-path H2S sensor based on tunable diode laser absorption spectroscopy (TDLAS) is developed, the laser used is a telecommunication near infrared distributed feed-back (DFB) tunable diode laser, combining with wavelength modulation specby combining optical fiber technique. An on-board reference cell provides on-line sensor calibration and almost maintenance-free operation. The sensor is suitable for large area field H2S monitoring application.

  8. Doppler-free two-photon absorption spectroscopy of rovibronic transition of naphthalene calibrated with an optical frequency comb

    Nishiyama, A.; Nakashima, K.; Matsuba, A.; Misono, M.

    2015-12-01

    We performed Doppler-free two-photon absorption spectroscopy of naphthalene using an optical frequency comb as a frequency reference. Rotationally resolved rovibronic spectra were observed, and absolute frequencies of the rovibronic transitions were determined with an uncertainty of several tens of kHz. The resolution and precision of our system are finer than the natural width of naphthalene. We assigned 1466 lines of the Q (Ka) Q (J) transition and calculated molecular constants. We attribute systematic spectral line shifts to the Coriolis interaction, and discuss the origin of the spectral linewidths.

  9. X-Ray Absorption Spectroscopy as a Probe of Microbial Sulfur Biochemistry: the Nature of Bacterial Sulfur Globules Revisited ▿

    George, Graham N.; Gnida, Manuel; Dennis A Bazylinski; Prince, Roger C.; Pickering, Ingrid J.

    2008-01-01

    The chemical nature of the sulfur in bacterial sulfur globules has been the subject of controversy for a number of years. Sulfur K-edge X-ray absorption spectroscopy (XAS) is a powerful technique for probing the chemical forms of sulfur in situ, but two groups have used it with very different conclusions. The root of the controversy lies with the different detection strategies used by the two groups, which result in very different spectra. This paper seeks to resolve the controversy. We exper...

  10. Broadband cavity-enhanced absorption spectroscopy in the ultraviolet spectral region for measurements of nitrogen dioxide and formaldehyde

    Washenfelder, R. A.; Attwood, A. R.; Flores, J. M.; Zarzana, K. J.; Rudich, Y.; Brown, S. S.

    2016-01-01

    Formaldehyde (CH2O) is the most abundant aldehyde in the atmosphere, and it strongly affects photochemistry through its photolysis. We describe simultaneous measurements of CH2O and nitrogen dioxide (NO2) using broadband cavity-enhanced absorption spectroscopy in the ultraviolet spectral region. The light source consists of a continuous-wave diode laser focused into a Xenon bulb to produce a plasma that emits high-intensity, broadband light. The plasma discharge is optically filtered and coupled into a 1 m optical cavity. The reflectivity of the cavity mirrors is 0.99930 ± 0.00003 (1- reflectivity = 700 ppm loss) at 338 nm, as determined from the known Rayleigh scattering of He and zero air. This mirror reflectivity corresponds to an effective path length of 1.43 km within the 1 m cell. We measure the cavity output over the 315-350 nm spectral region using a grating monochromator and charge-coupled device array detector. We use published reference spectra with spectral fitting software to simultaneously retrieve CH2O and NO2 concentrations. Independent measurements of NO2 standard additions by broadband cavity-enhanced absorption spectroscopy and cavity ring-down spectroscopy agree within 2 % (slope for linear fit = 1.02 ± 0.03 with r2 = 0.998). Standard additions of CH2O measured by broadband cavity-enhanced absorption spectroscopy and calculated based on flow dilution are also well correlated, with r2 = 0.9998. During constant mixed additions of NO2 and CH2O, the 30 s measurement precisions (1σ) of the current configuration were 140 and 210 pptv, respectively. The current 1 min detection limit for extinction measurements at 315-350 nm provides sufficient sensitivity for measurement of trace gases in laboratory experiments and ground-based field experiments. Additionally, the instrument provides highly accurate, spectroscopically based trace gas detection that may complement higher precision techniques based on non-absolute detection methods. In addition to

  11. Compact supercontinuum sources based on tellurite suspended core fibers for absorption spectroscopy beyond 2 μm

    Strutynski, Clément; Picot-Clémente, Jérémy; Désévédavy, Frédéric; Jules, Jean-Charles; Gadret, Grégory; Kibler, Bertrand; Smektala, Frédéric

    2016-07-01

    We present the experimental development of two compact supercontinuum laser sources based on tellurite suspended core fibers with and without tapering post-processing. The pumping scheme makes use of commercially-available nJ-level femtosecond and picosecond fiber lasers at 1.56 and 2.06 μm respectively. The resulting spectral broadening that occurs in a few tens-of-centimeters of tellurite fiber allows coverage of the convenient molecular fingerprint region between 2 and 3 μm. It is then exploited in a proof-of-principle experiment for methane spectroscopy measurements in the mid-infrared by means of the supercontinuum absorption spectroscopy technique. Experimental results are in fairly good agreement with both numerical simulations of supercontinuum generation and spectroscopic predictions of the HITRAN database.

  12. Optical absorption, 31P NMR, and photoluminescence spectroscopy study of copper and tin co-doped barium–phosphate glasses

    The optical and structural properties of 50P2O5:50BaO glasses prepared by melting have been investigated for additive concentrations of 10 and 1 mol% of CuO and SnO dopants. Absorption and photoluminescence spectroscopies were employed in the optical characterization, whereas structural properties were assessed by 31P nuclear magnetic resonance (NMR) spectroscopy. Residual Cu2+ was detectable by absorption spectroscopy for the highest concentration of CuO and SnO. More prominently, the optical data suggests contributions from both twofold-coordinated Sn centers and Cu+ ions to light absorption and emission in the glasses. The luminescence depends strongly on excitation wavelength for the highest concentration of dopants where a blue–white emission is observed under short-wavelength excitation (e.g., 260 nm) largely due to tin, while an orange luminescence is exhibited for longer excitation wavelengths (e.g., 360 nm) essentially due to Cu+ ions. On the other hand, dissimilar luminescent properties were observed in connection to Cu+ ions for the lowest concentration studied, as the copper ions were preferentially excited in a narrower range at shorter wavelengths near tin centers absorption. The structural analyses revealed the glass matrix to be composed essentially of Q2 (two bridging oxygens) and Q1 (one bridging oxygen) phosphate tetrahedra. A slight increase in the Q1/Q2 ratio reflected upon SnO doping alone suggests a major incorporation of tin into the glass network via P–O–Sn bonds, compatible with the 2-coordinated state attributed to the luminescent Sn centers. However, a significant increase in the Q1/Q2 ratio was indicated with the incorporation of copper at the highest concentration, consistent with a key role of the metal ions as network modifiers. Thus, the change in Cu+ optical properties concurs with different distributions of local environments around the ions induced by variation in metal ion concentration. Luminescence decay curve

  13. Stereochemistry of 16a-Hydroxyfriedelin and 3-Oxo-16-methylfriedel-16-ene Established by 2D NMR Spectroscopy

    Vagner Fernandes Knupp

    2009-02-01

    Full Text Available Friedelin (1, 3b-friedelinol (2, 28-hydroxyfriedelin (3, 16a-hydroxyfriedelin (4, 30-hydroxyfriedelin (5 and 16a,28-dihydroxyfriedelin (6 were isolated through fractionation of the hexane extract obtained from branches of Salacia elliptica. After a week in CDCl3 solution, 16a-hydroxyfriedelin (4 reacted turning into 3-oxo-16-methylfriedel-16-ene (7. This is the first report of a dehydration followed by a Nametkin rearrangement of a pentacyclic triterpene in CDCl3 solution occurring in the NMR tube. These seven pentacyclic triterpenes was identified through NMR spectroscopy and the stereochemistry of compound 4 and 7 was established by 2D NMR (NOESY spectroscopy and mass spectrometry (GC-MS. It is also the first time that all the 13C-NMR and 2D NMR spectral data are reported for compounds 4 and 7.

  14. Laser frequency locking based on the normal and abnormal saturated absorption spectroscopy of 87Rb

    Jian-Hong, Wan; Chang, Liu; Yan-Hui, Wang

    2016-04-01

    We present a practical method to avoid the mis-locking phenomenon in the saturated-absorption-spectrum laser-frequency-locking system and set up a simple theoretical model to explain the abnormal saturated absorption spectrum. The method uses the normal and abnormal saturated absorption spectra of the same transition 52S1/2, F = 2–52P3/2, F‧ = 3 saturated absorption of the 87Rb D2 resonance line. After subtracting these two signals with the help of electronics, we can obtain a spectrum with a single peak to lock the laser. In our experiment, we use the normal and inverse signals of the transitions 52S1/2, F = 2–52P3/2, F‧ = 3 saturated absorption of the 87Rb D2 resonance line to lock a 780-nm distributed feedback (DFB) diode laser. This method improves the long-term locking performance and is suitable for other kinds of diode lasers. Project supported by the National Natural Science Foundation of China (Grant No. 11174015).

  15. Interstellar X-Ray Absorption Spectroscopy of the Crab Pulsar with the LETGS

    Paerels, Frits; Weisskopf, Martin C.; Tennant, Allyn F.; ODell, Stephen L.; Swartz, Douglas A.; Kahn, Steven M.; Behar, Ehud; Becker, Werner; Whitaker, Ann F. (Technical Monitor)

    2001-01-01

    We study the interstellar X-ray absorption along the line of sight to the Crab Pulsar. The Crab was observed with the Low Energy Transmission Grating Spectrometer on the Chandra X-ray Observatory, and the pulsar, a point source, produces a full resolution spectrum. The continuum spectrum appears smooth, and we compare its parameters with other measurements of the pulsar spectrum. The spectrum clearly shows absorption edges due to interstellar Ne, Fe, and O. The O edge shows spectral structure that is probably due to O bound in molecules or dust. We search for near-edge structure (EXAFS) in the O absorption spectrum. The Fe L absorption spectrum is largely due to a set of unresolved discrete n=2-3 transitions in neutral or near-neutral Fe, and we analyze it using a new set of dedicated atomic structure calculations, which provide absolute cross sections. In addition to being interesting in its own right, the ISM absorption needs to be understood in quantitative detail in order to derive spectroscopic constraints on possible soft thermal radiation from the pulsar.

  16. Investigation of the Unoccupied Electronic Structure of UO2 with Bermstrahlung Isochromat Spectroscopy and X-Ray Absorption Spectroscopy

    UO2 is an important nuclear fuel for electrical power generation. Global goal : Actinides (5f electron systems) exhibit fascinating physical and chemical properties, due to 5f electron correlation, including the highly radioactive systems such as Pu. Onsite Instrumentation: A spectroscopic system containing spin resolved photoelectron spectroscopy (SRPES) and bremsstrahlung isochromat spectroscopy (BIS) has been built and commissioned at LLNL. ALS Instrumentation: The XAS was done on Beamline 8. Both Total Electron Yield (TEY) and Total Fluorescence Yield (TFY) were used. TFY is less surface sensitive than TEY. A combined experimental and theoretical study of Uranium Dioxide has been performed, including XAS, BIS, XPS and spectral simulations. The Conduction Bands or Unoccupied Density of States (UDOS) of UO2 are shown to be divided into two parts, the lower region being U5f-O2p and the upper region U6d-O2p. This means that UO2 is an f-f Mott Insulator, electron-correlated system. The keys to success with the XAS were the (1) the utilization of both TEY and TFY and (2) the accurate co-location of the uranium and oxygen states, which in turn hinged upon a proper calibration of the gratings of the beamline monochromator. The calibration of the gratings was greatly aided by the availibility of the O1s XAS from 1st, 2nd and 3rd order light. The success of this approach to differentiation of the Uranium UDOS into U5f and U6d components is of great importance and bodes well for its application to other actinide systems. Our ultimate goal remains Pu and its electron correlation.

  17. Measurement of transient gas flow parameters by diode laser absorption spectroscopy

    Bolshov, M. A.; Kuritsyn, Yu A.; Liger, V. V.; Mironenko, V. R.; Nadezhdinskii, A. I.; Ponurovskii, Ya Ya; Leonov, S. B.; Yarantsev, D. A.

    2015-04-01

    An absorption spectrometer based on diode lasers is developed for measuring two-dimension maps of temperature and water vapour concentration distributions in the combustion zones of two mixing supersonic flows of fuel and oxidiser in the single run regime. The method of measuring parameters of hot combustion zones is based on detection of transient spectra of water vapour absorption. The design of the spectrometer considerably reduces the influence of water vapour absorption along the path of a sensing laser beam outside the burning chamber. The optical scheme is developed, capable of matching measurement results in different runs of mixture burning. A new algorithm is suggested for obtaining information about the mixture temperature by constructing the correlation functions of the experimental spectrum with those simulated from databases. A two-dimensional map of temperature distribution in a test chamber is obtained for the first time under the conditions of plasma-induced combusion of the ethylene - air mixture.

  18. Time-Resolved Transient Absorption Spectroscopy and Luminescence in Undoped YVO4

    Yochum, H. M.; Grigorjeva, L.; Yochum, M. C. S.; Stevens, K. T.

    2005-03-01

    Yttrium orthovanadate (YVO4) is currently used as a solid-state laser host material and as a polarization component for fiber optic applications but suffers from crystal uniformity and discoloration problems. In an effort to increase our understanding of electron-hole traps and their role on the optical properties of YVO4, we have measured transient absorption spectra (1.1 eV - 3.5 eV) and relaxation kinetics following electron-hole pair generation induced by 270 keV, 10 ns electron pulses for probe delays 10 ns--10 microseconds. These experiments were completed on four Czochralski grown YVO4 samples with different levels of as-grown absorption in the 380 nm -- 430 nm region. For all samples, we find three transient absorption bands with similar energies. We have also measured the luminescence kinetics induced by ns electron pulses and by light pulses at 355 nm and 420 nm -- 600 nm.

  19. Simultaneous and continuous multiple wavelength absorption spectroscopy on nanoliter volumes based on frequency-division multiplexing fiber-loop cavity ring-down spectroscopy.

    Waechter, Helen; Munzke, Dorit; Jang, Angela; Loock, Hans-Peter

    2011-04-01

    We demonstrate a method for measuring optical loss simultaneously at multiple wavelengths with cavity ring-down spectroscopy (CRD). Phase-shift CRD spectroscopy is used to obtain the absorption of a sample from the phase lag of intensity modulated light that is entering and exiting an optical cavity. We performed dual-wavelength detection by using two different laser light sources and frequency-division multiplexing. Each wavelength is modulated at a separate frequency, and a broadband detector records the total signal. This signal is then demodulated by lock-in amplifiers at the corresponding two frequencies allowing us to obtain the phase-shift and therefore the optical loss at several wavelengths simultaneously without the use of a dispersive element. In applying this method to fiber-loop cavity ring-down spectroscopy, we achieve detection at low micromolar concentrations in a 100 nL liquid volume. Measurements at two wavelengths (405 and 810 nm) were performed simultaneously on two dyes each absorbing at mainly one of the wavelengths. The respective concentrations could be quantified independently in pure samples as well as in mixtures. No crosstalk between the two channels was observed, and a minimal detectable absorbance of 0.02 cm(-1) was achieved at 405 nm. PMID:21355542

  20. X-ray Absorption Spectroscopy of the Zinc-Binding Sites in the Class B2 Metallo-B-lactamsase ImiS from Aeromonas veronii bv. sobria

    Costello,A.; Sharma, N.; Yang, K.; Crowder, M.; Tierney, D.

    2006-01-01

    X-ray absorption spectroscopy was used to investigate the metal-binding sites of ImiS from Aeromonas veronii bv. sobria in catalytically active (1-Zn), product-inhibited (1-Zn plus imipenem), and inactive (2-Zn) forms. The first equivalent of zinc(II) was found to bind to the consensus Zn{sub 2} site. The reaction of 1-Zn ImiS with imipenem leads to a product-bound species, coordinated to Zn via a carboxylate group. The inhibitory binding site of ImiS was examined by a comparison of wild-type ImiS with 1 and 2 equiv of bound zinc. 2-Zn ImiS extended X-ray absorption fine structure data support a binding site that is distant from the active site and contains both one sulfur donor and one histidine ligand. On the basis of the amino acid sequence of ImiS and the crystal structure of CphA [Garau et al. (2005) J. Mol. Biol. 345, 785-795], we propose that the inhibitory binding site is formed by M146, found on the B2-distinct {alpha}3 helix, and H118, a canonical Zn{sub 1} ligand, proposed to help activate the nucleophilic water. The mutation of M146 to isoleucine abolishes metal inhibition. This is the first characterization of ImiS with the native metal Zn and establishes, for the first time, the location of the inhibitory metal site.

  1. Investigation of Cl corrosion products of iron archaeological artefacts using micro-focused synchrotron X-ray absorption spectroscopy

    Synchrotron-based micro-X-ray absorption spectroscopy is used in the present study to obtain chemical information at the microscopic scale such as coordination and oxidation state of Fe atoms in phases constituting corrosion products within archaeological iron artefacts buried in soil. This technique is required in order to answer questions about the iron corrosion process related to the presence of chloride, particularly for restoration and conservation of metallic artefacts of the cultural heritage. The samples available for X-ray microprobe analyses are cross sections from corroded iron archaeological objects. Previously, complementary techniques have been used such as μXRD and μRaman. This specific study applies micro-X-ray absorption spectroscopy to determine the spatial variation of the predominant Fe oxidation state and to identify the corresponding crystallographic phase. The analyses performed at Fe and Cl K-edges (μXANES) reveal the correlation between the valence distribution in the corrosion products and the evolution of the chloride concentration. In addition to the presence of the well-known iron oxyhydroxide β-FeOOH: akaganeite, we highlight the presence of another important phase, the β-Fe2(OH)3Clhydroxychloride. These important findings help to gain new insights concerning the influence of such phases in the iron corrosion mechanism within their precise characterization. (orig.)

  2. X-ray absorption and resonant photoelectron spectroscopy of epitaxial Fe-doped SrTiO3

    In recent years resistive switching in transition metal oxides received a lot of research interest due to the proposed application as non-volatile data memory. SrTiO3 serves as a model system for the investigation of resistive switching due to the valency change mechanism. Frequently, slightly Fe doping is used, as it has shown to improve the switching properties. The focus of this study is the effect of Fe-doping of SrTiO3 in thin epitaxial films. Thin film samples with Fe concentration of 2 at.% and 5 at.% were prepared by pulsed laser deposition at varying substrate temperatures. The surface morphology of the films is studied with AFM. X-ray absorption spectroscopy is performed in total-electron and auger-electron yield offering different probing depths. Significant variations of the Fe-L edge between bulk and interface as well as after annealing are observed and discussed in terms of integration into the lattice and evolution of secondary phases. Resonant photoelectron spectroscopy at the absorption edge of Ti, O and Fe was used to determine the spectral contributions to the valence band. Most noteworthy we find significant spectral weight above the valence band, which can be attributed to Fe-states.

  3. Can Femtosecond Transient Absorption Spectroscopy Predict the Potential of Small Molecules as Perspective Donors for Organic Photovoltaics?

    DiScipio, Regina; Sauve, Genevieve; Crespo-Hernández, Carlos E.

    2015-06-01

    The utility of a perspective donor or acceptor molecule for photoelectric applications is difficult to predict a priori. This hinders productive synthetic exploration and necessitates lengthy device optimization procedures for reasonable estimation of said molecule's applicability. Using femtosecond broadband transient absorption spectroscopy, supported by time-dependent density functional theory computations and steady-state-absorption and emission spectroscopies, we have characterized a family of perspective optoelectronic compounds, in an effort to predict their relative performance in organic photovoltaic devices from information accrued from excited-state dynamics and photophysical properties. A series of tetraphenylazadipyrromethene (ADP) complexes chelated with three different metal centers was investigated. We have determined that the chelating metal has little effect on the ground state properties of this family. However their excited state dynamics are strongly modulated by the metal. Specifically, the zinc-chelated ADP complex remains in the excited state tenfold longer than the cobalt or nickel complexes. We assert that this is key photophysical property that should make the zinc complex outperform the other two complexes in photovoltaic applications. This hypothesis is supported by preliminary power conversion efficiency results in devices.

  4. Establishment of the laser induced breakdown spectroscopy in a vacuum atmosphere for a accuracy improvement

    This report describes the fundamentals of the Laser Induced Breakdown Spectroscopy(LIBS), and it describes the quantitative analysis method in the vacuum condition to obtain a high measurement accuracy. The LIBS system employs the following major components: a pulsed laser, a gas chamber, an emission spectrometer, a detector, and a computer. When the output from a pulsed laser is focused onto a small spot on a sample, an optically induced plasma, called a laser-induced plasma (LIP) is formed at the surface. The LIBS is a laser-based sensitive optical technique used to detect certain atomic and molecular species by monitoring the emission signals from a LIP. This report was described a fundamentals of the LIBS and current states of research. And, It was described a optimization of measurement condition and characteristic analysis of a LIP by measurement of the fundamental metals. The LIBS system shows about a 0.63 ∼ 5.82% measurement errors and calibration curve for the 'Cu, Cr and Ni'. It also shows about a 5% less of a measurement errors and calibration curve for a Nd and Sm. As a result, the LIBS accuracy for a part was little improved than preexistence by the optimized condition

  5. Comparison of Nitric Oxide Concentrations in μs- and ns-Atmospheric Pressure Plasmas by UV Absorption Spectroscopy

    Peters, F.; Hirschberg, J.; Mertens, N.; Wieneke, S.; Viöl, W.

    2016-04-01

    In this paper, an absorption spectroscopy measurement method was applied on two atmospheric pressure plasma sources to determine their production of nitric oxide. The concentrations are essential for evaluating the plasma sources based on the principle of the Dielectric Barrier Discharge (DBD) for applications in plasma medicine. The described method is based on a setup with an electrodeless discharge lamp filled with a mixture of oxygen and nitrogen. One of the emitted wavelengths is an important resonance wavelength of nitric oxide (λ = 226.2 nm). By comparing the absorption behaviour at the minimum and maximum of the spectral absorption cross section of nitric oxide around that wavelength, and measuring the change in intensity by the absorbing plasma, the concentration of nitric oxide inside the plasma can be calculated. The produced nitric oxide concentrations depend on the pulse duration and are in the range of 180 ppm to 1400 ppm, so that a distance of about 10cm to the respiratory tract is enough to conform to the VDI Guideline 2310.

  6. Thin film limit correction method to the surface defective layer in low absorption spectroscopy

    Remeš, Zdeněk; Holovský, Jakub; Purkrt, Adam; Stuchlík, Jiří

    2015-01-01

    Roč. 7, č. 4 (2015), s. 343-346. ISSN 2164-6627 R&D Projects: GA ČR(CZ) GA14-05053S; GA MŠk(CZ) LD14011 Institutional support: RVO:68378271 Keywords : thin film s * optical properties * hydrogenated amorphous silicon * photothermal deflection spectroscopy Subject RIV: BM - Solid Matter Physics ; Magnetism

  7. Application of FT-IR Absorption Spectroscopy to Characterize Waste and Biofuels for Pyrolysis and Gasification.

    Kalisz, S.; Svoboda, Karel; Robak, Z.; Baxter, D.; Andersen, L. K.

    -: -, 2007, s. 1-12. [International Conference Fuel from Waste 2007 /6./. Krynica (PL), 24.10.2007-26.10.2007] Institutional research plan: CEZ:AV0Z40720504 Keywords : spectroscopy * waste bio-fuels * gasification Subject RIV: CI - Industrial Chemistry, Chemical Engineering

  8. Photoelectron and UV absorption spectroscopy for determination of electronic configurations of negative molecular ions: Chlorophenols

    Tseplin, E.E. [Institute of Molecular and Crystal Physics, Ufa Research Centre, Russian Academy of Sciences, October Prospect 151, Ufa 450075 (Russian Federation)], E-mail: tzeplin@mail.ru; Tseplina, S.N.; Tuimedov, G.M.; Khvostenko, O.G. [Institute of Molecular and Crystal Physics, Ufa Research Centre, Russian Academy of Sciences, October Prospect 151, Ufa 450075 (Russian Federation)

    2009-04-15

    The photoelectron and UV absorption spectra of p-, m-, and o-chlorophenols in the gas phase have been obtained. On the basis of DFT B3LYP/6-311++G(d, p) calculations, the photoelectron bands have been assigned to occupied molecular orbitals. From the TDDFT B3LYP/6-311++G(d, p) calculation results, the UV absorption bands have been assigned to excited singlet states of the molecules under investigation. For each excited state a dominant transition was found. It has been shown that the energies of these singlet transitions correlate with the energy differences between the ground-state molecular orbitals participating in them. Using the UV spectra interpretation, the electronic states of molecular anions detected earlier for the same compounds by means of the resonant electron capture mass-spectrometry have been determined.

  9. Wavelength Modulation Absorption Spectroscopy Using a Frequency-Quadruped Current-Modulated System

    A wavelength modulation absorption spectrometry (WMAS) with a frequency-quadruped system is demonstrated. The frequency-quadruped system consists of a two-frequency doubled external enhancement cavity with KNO3 and BBO crystals, and a current-modulated 906-nm single mode external cavity diode laser (ECDL), which generates the tunable wavelength modulated radiation at 226.7 nm used to detect the NO absorption line that belongs to the combined Q22(10.5) and QR12(10.5) lines of 7(0, 0) band within the A2Σ+ – X2II electronic transition system. The 1st, 2nd and 3rd harmonic spectra are accomplished to show that it is possible to detect samples using the frequency quadruped system combined with the WMAS technique that can find practical applicability in the future

  10. Single shot near edge x-ray absorption fine structure spectroscopy in the laboratory

    Mantouvalou, I.; Witte, K.; Martyanov, W.; Jonas, A.; Grötzsch, D.; Streeck, C.; Löchel, H.; Rudolph, I.; Erko, A.; Stiel, H.; Kanngießer, B.

    2016-05-01

    With the help of adapted off-axis reflection zone plates, near edge X-ray absorption fine structure spectra at the C and N K-absorption edge have been recorded using a single 1.2 ns long soft X-ray pulse. The transmission experiments were performed with a laser-produced plasma source in the laboratory rendering time resolved measurements feasible independent on large scale facilities. A resolving power of E/ΔE ˜ 950 at the respective edges could be demonstrated. A comparison of single shot spectra with those collected with longer measuring time proves that all features of the used reference samples (silicon nitrate and polyimide) can be resolved in 1.2 ns. Hence, investigations of radiation sensitive biological specimen become possible due to the high efficiency of the optical elements enabling low dose experiments.

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

    Coe, J P

    2015-01-01

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

  12. Determination of metallic impurities in raw materials for radioisotope production by atomic absorption spectroscopy

    Atomic absorption spectrometry has been used for the determination of traces of calcium in scandium oxide, copper in zinc, iron in cobalt oxide, manganese In ferric oxide, nickel in copper and zinc in gallium oxide. The influences on the sensitivities arising from the hollow cathode currents, the gas pressures and the acid concentrations have been considered. A study of the interferences from the metallic matrices has also been performed, the interference due to the absorption of the manganese radiation by the atoms of iron being the most outstanding . In order to remove the interfering elements and increase sensitivity, pre-concentration methods have been tested. The addition methods has also been used. (Author) 14 refs

  13. Excited-State Dynamics of Carotenoids Studied by Femtosecond Transient Absorption Spectroscopy

    Lee, Ingu; Pang, Yoonsoo [Department of Physics and Photon Science, Gwangju (Korea, Republic of); Lee, Sebok [Gwangju Institute of Science and Technology, Gwangju (Korea, Republic of)

    2014-03-15

    Carotenoids, natural antenna pigments in photosynthesis share a symmetric backbone of conjugated polyenes. Contrary to the symmetric and almost planar geometries of carotenoids, excited state structure and dynamics of carotenoids are exceedingly complex. In this paper, recent infrared and visible transient absorption measurements and excitation dependent dynamics of 8'-apo-β-caroten-8'-al and 7',7'-dicyano-7'-apo-β-carotene will be reviewed. The recent visible transient absorption measurements of 8'-apo-β-caroten-8'-al in polar and nonpolar solvents will also be introduced to emphasize the complex excited-state dynamics and unsolved problems in the S{sub 2} and S{sub 1} excited states.

  14. X-ray absorption fine structure spectroscopy and X-ray diffraction study of cementitious materials derived from coal combustion by-products

    Cementitious materials derived from coal combustion by-products have been investigated by means of X-ray diffraction (XRD) and S and Ca K-edge X-ray absorption fine structure (XAFS) spectroscopy. The XRD analysis revealed that these materials are a complex mixture of a small amount of quartz [SiO2] and three calcium-bearing compounds: hannebachite [CaSO3·1/2H2O], gypsum [CaSO4·2H2O] and ettringite [(Ca6(Al(OH)6)2(SO4)3·26H2O)]. Analysis of the S XAFS data focused on deconvolution of the X-ray absorption near-edge structure (XANES) regions of the spectra. This analysis established that sulfate and sulfite are the two major sulfur forms, with a minor thiophenic component contained in unburned carbon in the fly ash. Increasing sulfate and decreasing sulfite correlated well with increasing gypsum and ettringite and decreasing hannebachite content in the samples. Different calcium compounds were identified primarily through simple comparison of the Ca K-edge XANES and radial structure functions (RSFs) of the cementitious samples with those of reference compounds. Because of the complex coordination chemistry of calcium in these materials, it was difficult to obtain detailed local atomic environment information around calcium beyond the first Ca-O peak. Analysis of the extended X-ray absorption fine structure (EXAFS) and the RSF gave average Ca-O distances in the range 2.44-2.5 A, with each calcium atom surrounded roughly by eight oxygen atoms. In certain samples, the average Ca-O distances were close to that in ettringite (2.51 A), suggesting that these samples have higher ettringite content. The results of S and Ca K-edges XAFS and the XRD data were in reasonable agreement

  15. Near Edge X-ray Absorption Fine Structure Spectroscopy Studies of Single-Crystalline V2O5 Nanowire Arrays

    Velazquez, J.; Jaye, C; Fischer, D; Banerjee, S

    2009-01-01

    Near edge X-ray absorption fine structure (NEXAFS) spectroscopy is used to precisely probe the alignment, uniformity in crystal growth direction, and electronic structure of single-crystalline V2O5 nanowire arrays prepared by a cobalt-catalyzed vapor transport process. The dipole selection rules operational for core-level electron spectroscopy enable angle-dependent NEXAFS spectroscopy to be used as a sensitive probe of the anisotropy of these systems and provides detailed insight into bond orientation and the symmetry of the frontier orbital states. The experimental spectra are matched to previous theoretical predictions and allow experimental verification of features such as the origin of the split-off conduction band responsible for the semiconducting properties of V2O5 and the strongly anisotropic nature of vanadyl-oxygen-derived (VO) states thought to be involved in catalysis. The strong anisotropy observed across thousands of nanowires in the NEXAFS measurements clearly demonstrates the uniformity of crystal growth direction in these nanowire arrays.

  16. Near-edge X-ray absorption fine-structure spectroscopy of naphthalene diimide-thiophene co-polymers

    Gann, Eliot; McNeill, Christopher R., E-mail: christopher.mcneill@monash.edu [Department of Materials Engineering, Monash University, Wellington Road, Clayton, Victoria 3800 (Australia); Szumilo, Monika; Sirringhaus, Henning [Cavendish Laboratory, University of Cambridge, JJ Thomson Avenue, Cambridge CB3 0HE (United Kingdom); Sommer, Michael [Institute of Macromolecular Chemistry, University of Freiburg, Stefan-Meier-Str. 31, 79104 Freiburg (Germany); Maniam, Subashani; Langford, Steven J. [School of Chemistry, Monash University, Wellington Road, Clayton, Victoria 3800 (Australia); Thomsen, Lars [Australian Synchrotron, 800 Blackburn Road, Clayton, Victoria 3168 (Australia)

    2014-04-28

    Near-edge X-ray absorption fine-structure (NEXAFS) spectroscopy is an important tool for probing the structure of conjugated polymer films used in organic electronic devices. High-performance conjugated polymers are often donor-acceptor co-polymers which feature a repeat unit with multiple functional groups. To facilitate better application of NEXAFS spectroscopy to the study of such materials, improved understanding of the observed NEXAFS spectral features is required. In order to examine how the NEXAFS spectrum of a donor-acceptor co-polymer relates to the properties of the sub-units, a series of naphthalene diimide-thiophene-based co-polymers have been studied where the nature and length of the donor co-monomer has been systematically varied. The spectra of these materials are compared with that of a thiophene homopolymer and naphthalene diimide monomer enabling peak assignment and the influence of inter-unit electronic coupling to be assessed. We find that while it is possible to attribute peaks within the π* manifold as arising primarily due to the naphthalene diimide or thiophene sub-units, very similar dichroism of these peaks is observed indicating that it may not be possible to separately probe the molecular orientation of the separate sub-units with carbon K-edge NEXAFS spectroscopy.

  17. Near-edge X-ray absorption fine-structure spectroscopy of naphthalene diimide-thiophene co-polymers

    Near-edge X-ray absorption fine-structure (NEXAFS) spectroscopy is an important tool for probing the structure of conjugated polymer films used in organic electronic devices. High-performance conjugated polymers are often donor-acceptor co-polymers which feature a repeat unit with multiple functional groups. To facilitate better application of NEXAFS spectroscopy to the study of such materials, improved understanding of the observed NEXAFS spectral features is required. In order to examine how the NEXAFS spectrum of a donor-acceptor co-polymer relates to the properties of the sub-units, a series of naphthalene diimide-thiophene-based co-polymers have been studied where the nature and length of the donor co-monomer has been systematically varied. The spectra of these materials are compared with that of a thiophene homopolymer and naphthalene diimide monomer enabling peak assignment and the influence of inter-unit electronic coupling to be assessed. We find that while it is possible to attribute peaks within the π* manifold as arising primarily due to the naphthalene diimide or thiophene sub-units, very similar dichroism of these peaks is observed indicating that it may not be possible to separately probe the molecular orientation of the separate sub-units with carbon K-edge NEXAFS spectroscopy

  18. Environmental Chamber Study of Atmospheric Chemistry and Secondary Organic Aerosol Formation Using Cavity Enhanced Absorption Spectroscopy

    Liu, Yingdi

    2011-01-01

    Air pollution and global climate change are important environmental issues that affect our society. Deeper understanding of atmospheric chemistry is required to understand these problems and to develop effective control strategies. Environmental chambers have been used for the past few decades to study atmospheric chemistry and investigate processes leading to secondary pollutant formation. This thesis work provides two different high sensitivity real time cavity enhance absorption spectrosco...

  19. Quantum cascade laser absorption spectroscopy - A new method to study molecular plasma components

    The recent development of quantum cascade lasers (QCLs) offers an attractive new option for the monitoring and control of industrial plasma processes and for trace-gas analysis as well as for highly time-resolved studies on the kinetics of plasma processes. The contribution reviews selected examples of the application of QCLs for infrared absorption studies in basic research and for plasma monitoring and control in industry.

  20. Quantum cascade laser absorption spectroscopy - A new method to study molecular plasma components

    Roepcke, J; Glitsch, S; Hempel, F; Lang, N; Welzel, S [INP Greifswald, F.-Hausdorff-Str. 2, 17489 Greifswald (Germany); Davies, P [University of Cambridge, Lensfield Road, Cambridge CB2 1EW (United Kingdom); Rousseau, A [LPP, Ecole Polytechnique, CNRS, 91128 Palaiseau Cedex (France); Wege, S, E-mail: roepcke@inp-greifswald.d [Plasway, Hauptstr. 7a, 01328 Dresden (Germany)

    2010-05-01

    The recent development of quantum cascade lasers (QCLs) offers an attractive new option for the monitoring and control of industrial plasma processes and for trace-gas analysis as well as for highly time-resolved studies on the kinetics of plasma processes. The contribution reviews selected examples of the application of QCLs for infrared absorption studies in basic research and for plasma monitoring and control in industry.

  1. Computer programs in BASIC language for atomic absorption flame spectroscopy. Part 1. Operating instructions

    These instructions describe how to use three BASIC language programs to process data from atomic absorption spectrophotometers operated in the flame mode. These programs will also control an automatic sampler if desired. The instructions cover loading the programs, responding to computer prompts, choosing among various options for processing the data, operating the automatic sampler, and producing reports. How the programs differ is also explained. Examples of computer/operator dialogue are presented for typical cases

  2. Total absorption γ-ray spectroscopy of beta delayed neutron emitters

    Valencia, E.; Algora, A.; Tain, J. L.; Rice, S.; Agramunt, J.; Zakari-Issoufou, A.-A.; Porta, A.; Fallot, M.; Jordan, M. D.; Molina, F.; Estevez, E.; Bowry, M.; Bui, V. M.; Caballero-Folch, R.; Cano-Ott, D.; Eloma, V.; Eronen, T.; Garcia, A.; Gomez-Hornillos, M. B.; Gorlychev, V.; Hakala, J.; Jokinen, A.; Kondev, F. G.; Martinez, T.; Moore, I.; Rissanen, J.; Ńystö, J.; Penttilä, H.; Kankainen, A.; Rubio, B.; Gelletly, W.; Perez, A.; Podolyak, Zs.; Regan, P. H.; Farrelly, G. F.; Weber, C.; Mendoza, E.; Igisol People

    2013-06-01

    Preliminary results of the data analysis of the beta decay of 94Rb using a novel - segmented- total absorption spectrometer are shown in this contribution. This result is part of a systematic study of important contributors to the decay heat problem in nuclear reactors. In this particular case the goal is to determine the beta intensity distribution below the neutron separation energy and the gamma/beta competition above.

  3. Observation of Charged Excitons in Hole-Doped Carbon Nanotubes Using Photoluminescence and Absorption Spectroscopy

    Matsunaga, Ryusuke; Matsuda, Kazunari; Kanemitsu, Yoshihiko

    2011-01-01

    We report the first observation of trions (charged excitons), three-particle bound states consisting of one electron and two holes, in hole-doped carbon nanotubes at room temperature. When p-type dopants are added to carbon nanotube solutions, the photoluminescence and absorption peaks of the trions appear far below the E11 bright exciton peak, regardless of the dopant species. The unexpectedly large energy separation between the bright excitons and the trions is attributed to the strong elec...

  4. Observation of charged excitons in hole-doped carbon nanotubes using photoluminescence and absorption spectroscopy

    Matsunaga, Ryusuke; Matsuda, Kazunari; Kanemitsu, Yoshihiko

    2010-01-01

    We report the first observation of trions (charged excitons), three-particle bound states consisting of one electron and two holes, in hole-doped carbon nanotubes at room temperature. When p-type dopants are added to carbon nanotube solutions, the photoluminescence and absorption peaks of the trions appear far below the E11 bright exciton peak, regardless of the dopant species. The unexpectedly large energy separation between the bright excitons and the trions is attributed to the strong elec...

  5. Phase reconstruction of strong-field excited systems by transient-absorption spectroscopy

    Liu, Z; Ott, C; Meyer, K; Mi, Y; Harman, Z; Keitel, C H; Pfeifer, T

    2015-01-01

    We study the evolution of a V-type three-level system, whose two resonances are coherently excited and coupled by two ultrashort laser pump and probe pulses, separated by a varying time delay. We relate the quantum dynamics of the excited multi-level system to the absorption spectrum of the transmitted probe pulse. In particular, by analyzing the quantum evolution of the system, we interpret how atomic phases are differently encoded in the time-delay-dependent spectral absorption profiles when the pump pulse either precedes or follows the probe pulse. We experimentally apply this scheme to atomic Rb, whose fine-structure-split $5s\\,^2S_{1/2}\\rightarrow 5p\\,^2P_{1/2}$ and $5s\\,^2S_{1/2}\\rightarrow 5p\\,^2P_{3/2}$ transitions are driven by the combined action of a pump pulse of variable intensity and a delayed probe pulse. The provided understanding of the relationship between quantum phases and absorption spectra represents an important step towards full time-dependent phase reconstruction (quantum holography) ...

  6. Quick scanning monochromator for millisecond in situ and in operando X-ray absorption spectroscopy.

    Müller, O; Lützenkirchen-Hecht, D; Frahm, R

    2015-09-01

    The design and capabilities of a novel Quick scanning Extended X-ray Absorption Fine Structure (QEXAFS) monochromator are presented. The oscillatory movement of the crystal stage is realized by means of a unique open-loop driving scheme operating a direct drive torque motor. The entire drive mechanics are installed inside of a goniometer located on the atmospheric side of the vacuum chamber. This design allows remote adjustment of the oscillation frequency and spectral range, giving complete control of QEXAFS measurements. It also features a real step-scanning mode, which operates without a control loop to prevent induced vibrations. Equipped with Si(111) and Si(311) crystals on a single stage, it facilitates an energy range from 4.0 keV to 43 keV. Extended X-ray absorption fine structure spectra up to k = 14.4 Å(-1) have been acquired within 17 ms and X-ray absorption near edge structure spectra covering more than 200 eV within 10 ms. The achieved data quality is excellent as shown by the presented measurements. PMID:26429455

  7. Quick scanning monochromator for millisecond in situ and in operando X-ray absorption spectroscopy

    Müller, O.; Lützenkirchen-Hecht, D.; Frahm, R.

    2015-09-01

    The design and capabilities of a novel Quick scanning Extended X-ray Absorption Fine Structure (QEXAFS) monochromator are presented. The oscillatory movement of the crystal stage is realized by means of a unique open-loop driving scheme operating a direct drive torque motor. The entire drive mechanics are installed inside of a goniometer located on the atmospheric side of the vacuum chamber. This design allows remote adjustment of the oscillation frequency and spectral range, giving complete control of QEXAFS measurements. It also features a real step-scanning mode, which operates without a control loop to prevent induced vibrations. Equipped with Si(111) and Si(311) crystals on a single stage, it facilitates an energy range from 4.0 keV to 43 keV. Extended X-ray absorption fine structure spectra up to k = 14.4 Å-1 have been acquired within 17 ms and X-ray absorption near edge structure spectra covering more than 200 eV within 10 ms. The achieved data quality is excellent as shown by the presented measurements.

  8. Subaru high resolution spectroscopy of complex metal absorption lines of QSO HS1603+3820

    Misawa, T; Takada-Hidai, M; Wang, Y; Kashikawa, N; Iye, M; Tanaka, I; Misawa, Toru; Yamada, Toru; Takada-Hidai, Masahide; Wang, Yiping; Kashikawa, Nobunari; Iye, Masanori; Tanaka, Ichi

    2002-01-01

    We present a high resolution spectrum of the quasar, HS1603+3820 (z_em=2.542), observed with the High Dispersion Spectrograph (HDS) on Subaru Telescope. This quasar, first discovered in the Hamburg/CfA Quasar Survey, has 11 C IV lines at 1.96 2.29 and resolves some of them into multiple narrow components with b 65 km/s). We use three properties of C IV lines, specifically, time variability, covering factor, and absorption line profile, to classify them into quasar intrinsic absorption lines (QIALs) and spatially intervening absorption lines (SIALs). The C IV lines at 2.42 < z_abs < 2.45 are classified as QIALs in spite of their large velocity shifts from the quasar. Perhaps they are produced by gas clouds ejected from the quasar with the velocity of v_ej = 8000 km/s -- 10000 km/s. On the other hand, three C IV lines at 2.48 < z_abs < 2.55 are classified as SIALs, which suggests there exist intervening absorbers near the quasar. We, however, cannot rule out QIALs for the two lines at z_abs ~ 2.54...

  9. Terahertz Absorption Spectroscopy of Benzamide, Acrylamide, Caprolactam, Salicylamide, and Sulfanilamide in the Solid State

    Ye Jiang

    2014-01-01

    Full Text Available Terahertz (THz absorption spectra of the similarly structured molecules with amide groups including benzamide, acrylamide, caprolactam, salicylamide, and sulfanilamide in the solid phase at room temperature and 7.8 K for salicylamide are reported and compared to infrared vibrational spectral calculations using density functional theory. The results of THz absorption spectra show that the molecules have characteristic bands in the region of 0.2–2.6 THz (~7–87 cm−1. THz technique can be used to distinguish different molecules with amide groups. In the THz region benzamide has three bands at 0.83, 1.63, and 1.73 THz; the bands are located at 1.44 and 2.00 THz for acrylamide; the bands at 1.24, 1.66 and 2.12 THz are observed for caprolactam. The absorption bands are located at 1.44, 1.63, and 2.39 THz at room temperature, and at 1.22, 1.46, 1.66, and 2.41 THz at low temperature for salicylamide. The bands at 1.63, 1.78, 2.00, and 2.20 THz appear for sulfanilamide. These bands in the THz region may be related to torsion, rocking, wagging, and other modes of different groups in the molecules.

  10. Long-slit spectroscopy of near-ultraviolet NH absorption in the nuclei of M31

    Using the Canada-France-Hawaii Telescope long-slit near-ultraviolet spectra of the central regions of M31 and M32 have been obtained. The Delta v = 0 NH absorption bands near 3360 A are detected out to distances of about 32 arcsec in M31 and about 15 arcsec in M32, and the spatial behavior of these features in each galaxy has been studied. NH absorption in M31 appears to vary in a complicated manner with respect to radial distance from the galaxy center, and there is no evidence for a systematic gradient. Moreover, the variations in NH strength appear to be more or less symmetric on a north/south axis about the central nucleus of M31. As for M32, NH absoption becomes progressively stronger with increasing distance from the center of this galaxy. Various explanations for the radial behavior of NH absorption in each galaxy are considered; these results may reflect changes in the relative contributions of early-type stars to the near-ultraviolet light output, or a radial variation in N/Fe. 43 refs

  11. Long-slit spectroscopy of near-ultraviolet NH absorption in the nuclei of M31

    Davidge, T.J.; De Robertis, M.M.; Yee, H.K.C. (Canada-France-Hawaii Telescope Corp., Kamuela, HI (USA) York Univ., North York (Canada) Toronto Univ. (Canada))

    1990-10-01

    Using the Canada-France-Hawaii Telescope long-slit near-ultraviolet spectra of the central regions of M31 and M32 have been obtained. The Delta v = 0 NH absorption bands near 3360 A are detected out to distances of about 32 arcsec in M31 and about 15 arcsec in M32, and the spatial behavior of these features in each galaxy has been studied. NH absorption in M31 appears to vary in a complicated manner with respect to radial distance from the galaxy center, and there is no evidence for a systematic gradient. Moreover, the variations in NH strength appear to be more or less symmetric on a north/south axis about the central nucleus of M31. As for M32, NH absoption becomes progressively stronger with increasing distance from the center of this galaxy. Various explanations for the radial behavior of NH absorption in each galaxy are considered; these results may reflect changes in the relative contributions of early-type stars to the near-ultraviolet light output, or a radial variation in N/Fe. 43 refs.

  12. Structural characterization of the Co/Cr multilayers by x-ray-absorption spectroscopy

    We have performed Cr and Co K-edge x-ray-absorption measurements to investigate the dependence of local electronic and atomic structures on the Cr-layer thickness in epitaxial Co(11-bar00) (40 A)/Cr(211) (tCr) (tCr=2, 3, 5, 7, and 9 A) multilayers. The Cr K x-ray-absorption near-edge fine structure (XANES) spectra of the Co/Cr multilayers indicate an abrupt transition of the Cr layer from hcp to bcc structure when the thickness of the Cr layer is increased to exceed ∼5 A or three atomic layers. Our results offer an upper limit for the ability of the Co/Cr interface to stabilize the hcp structure in the thin Cr layer. The numbers of nearest-neighbor and next-nearest-neighbor atoms in the Cr and Co layers determined by extended x-ray-absorption fine-structure measurements performed at the Cr and Co K edge, respectively, are consistent with the XANES results

  13. 1913–2013 – The centennial of X-ray absorption spectroscopy (XAS): Evidences about a question still open

    Mottana, Annibale, E-mail: annibale.mottana@uniroma3.it [Università degli Studi Roma Tre, Dipartimento di Scienze, Largo S. Leonardo Murialdo 1, I-00146 Roma (Italy); Istituto Nazionale di Fisica Nucleare, Laboratori Nazionali di Frascati, Via E. Fermi 40, I-00044 Frascati, RM (Italy)

    2014-10-15

    Highlights: • X-ray Absorption Spectroscopy (XAS) cannot be dated exactly as for its birth. • The assumed discoverer, M. de Broglie, was preceded by J. Herweg in the submission. • However, both their spectra were found to be mistaken. • Before the work of W. Stenström and H. Fricke no sure evidence of XAS is published. • The solution is, probably, taking October 1, 1918 as XAS fictitious birthday. - Abstract: In 1913 J. Herweg first (June 30) and M. de Broglie slightly later (November 17) claimed the discovery of a series of spots and lines closely following the main absorption edges of heavy metals, which they interpreted as the proof of the existence of X-ray spectra analogous to light spectra. In the following year they documented their discoveries via photographic plates. However, they were both discredited: Herweg by G.E.M. Jauncey, who showed that his spectra, taken on Pt and W, did not obey Moseley's rule; de Broglie by W.H. Bragg, M. Siegbahn and E. Wagner, who showed that his lines were in fact the fluorescence lines of the Ag and Br constituents of the photographic emulsion. Consequently, W. Stenström's description (sent to publisher on July 2, 1918) of certain photographically recorded and graphically rendered modulations near the M-series edges of heavy metals may possibly be the first published evidence of true X-ray absorption spectra. Indeed, they were interpreted as such by W. Kossel (1920) in his seminal theoretical paper. Otherwise, H. Fricke's table, although printed in 1920, which exhibits the photographic plate of sulphur absorption dated October 1, 1918, and its graphical rendering by a photometric method, is the first unequivocally dated evidence of recorded modulations at a XAS K-edge.

  14. Analysis of functional groups in atmospheric aerosols by infrared spectroscopy: sparse methods for statistical selection of relevant absorption bands

    Takahama, Satoshi; Ruggeri, Giulia; Dillner, Ann M.

    2016-07-01

    Various vibrational modes present in molecular mixtures of laboratory and atmospheric aerosols give rise to complex Fourier transform infrared (FT-IR) absorption spectra. Such spectra can be chemically informative, but they often require sophisticated algorithms for quantitative characterization of aerosol composition. Naïve statistical calibration models developed for quantification employ the full suite of wavenumbers available from a set of spectra, leading to loss of mechanistic interpretation between chemical composition and the resulting changes in absorption patterns that underpin their predictive capability. Using sparse representations of the same set of spectra, alternative calibration models can be built in which only a select group of absorption bands are used to make quantitative prediction of various aerosol properties. Such models are desirable as they allow us to relate predicted properties to their underlying molecular structure. In this work, we present an evaluation of four algorithms for achieving sparsity in FT-IR spectroscopy calibration models. Sparse calibration models exclude unnecessary wavenumbers from infrared spectra during the model building process, permitting identification and evaluation of the most relevant vibrational modes of molecules in complex aerosol mixtures required to make quantitative predictions of various measures of aerosol composition. We study two types of models: one which predicts alcohol COH, carboxylic COH, alkane CH, and carbonyl CO functional group (FG) abundances in ambient samples based on laboratory calibration standards and another which predicts thermal optical reflectance (TOR) organic carbon (OC) and elemental carbon (EC) mass in new ambient samples by direct calibration of infrared spectra to a set of ambient samples reserved for calibration. We describe the development and selection of each calibration model and evaluate the effect of sparsity on prediction performance. Finally, we ascribe

  15. Link between K absorption edges and thermodynamic properties of warm dense plasmas established by an improved first-principles method

    Zhang, Shen; Zhao, Shijun; Kang, Wei; Zhang, Ping; He, Xian-Tu

    2016-03-01

    A precise calculation that translates shifts of x-ray K absorption edges to variations of thermodynamic properties allows quantitative characterization of interior thermodynamic properties of warm dense plasmas by x-ray absorption techniques, which provides essential information for inertial confinement fusion and other astrophysical applications. We show that this interpretation can be achieved through an improved first-principles method. Our calculation shows that the shift of K edges exhibits selective sensitivity to thermal parameters and thus would be a suitable temperature index to warm dense plasmas. We also show with a simple model that the shift of K edges can be used to detect inhomogeneity inside warm dense plasmas when combined with other experimental tools.

  16. Correction method to the surface defective layer in low absorption spectroscopy

    Remeš, Zdeněk; Holovský, Jakub

    Praha : Czechoslovak Association for Crystal Growth (CSACG), 2014 - (Kožíšek, Z.; Nitsch, K.). s. 35-35 ISBN 978-80-260-6599-9. [Joint Seminar Development of Materials Science in Research and Education /24./. 08.09.2014-12.09.2014, Lednice] R&D Projects: GA ČR(CZ) GA14-05053S Institutional support: RVO:68378271 Keywords : optical spectroscopy * thin films Subject RIV: BH - Optics, Masers, Lasers

  17. Solvation structure of the halides from x-ray absorption spectroscopy

    Antalek, Matthew; Pace, Elisabetta; Hedman, Britt; Hodgson, Keith O.; Chillemi, Giovanni; Benfatto, Maurizio; Sarangi, Ritimukta; Frank, Patrick

    2016-07-01

    Three-dimensional models for the aqueous solvation structures of chloride, bromide, and iodide are reported. K-edge extended X-ray absorption fine structure (EXAFS) and Minuit X-ray absorption near edge (MXAN) analyses found well-defined single shell solvation spheres for bromide and iodide. However, dissolved chloride proved structurally distinct, with two solvation shells needed to explain its strikingly different X-ray absorption near edge structure (XANES) spectrum. Final solvation models were as follows: iodide, 8 water molecules at 3.60 ± 0.13 Å and bromide, 8 water molecules at 3.40 ± 0.14 Å, while chloride solvation included 7 water molecules at 3.15 ± 0.10 Å, and a second shell of 7 water molecules at 4.14 ± 0.30 Å. Each of the three derived solvation shells is approximately uniformly disposed about the halides, with no global asymmetry. Time-dependent density functional theory calculations simulating the chloride XANES spectra following from alternative solvation spheres revealed surprising sensitivity of the electronic state to 6-, 7-, or 8-coordination, implying a strongly bounded phase space for the correct structure during an MXAN fit. MXAN analysis further showed that the asymmetric solvation predicted from molecular dynamics simulations using halide polarization can play no significant part in bulk solvation. Classical molecular dynamics used to explore chloride solvation found a 7-water solvation shell at 3.12 (-0.04/+0.3) Å, supporting the experimental result. These experiments provide the first fully three-dimensional structures presenting to atomic resolution the aqueous solvation spheres of the larger halide ions.

  18. Absorption Spectroscopy Analysis of Calcium-Phosphate Glasses Highly Doped with Monovalent Copper.

    Jiménez, José A

    2016-06-01

    CaO-P2 O5 glasses with high concentrations of monovalent copper ions were prepared by a simple melt-quench method through CuO and SnO co-doping. Spectroscopic characterization was carried out by optical absorption with the aim of analyzing the effects of Cu(+) ions on the optical band-gap energies, which were estimated on the basis of indirect-allowed transitions. The copper(I) content is estimated in the CuO/SnO-containing glasses after the assessment of the concentration dependence of Cu(2+) absorption in the visible region for CuO singly doped glasses. An exponential dependence of the change in optical band gaps (relative to the host) with Cu(+) concentration is inferred up to about 10 mol %. However, the entire range is divided into two distinct linear regions that are characterized by different rates of change with respect to concentration: 1) below 5 mol %, where the linear dependence presents a relatively high magnitude of the slope; and 2) from 5-10 mol %, where a lower magnitude of the slope is manifested. With increasing concentration, the mean Cu(+) -Cu(+) interionic distance decreases, thereby decreasing the sensitivity of monovalent copper for light absorption. The decrease in optical band-gap energies is ultimately shown to follow a linear dependence with the interionic distance, suggesting the potential of the approach to gauge the concentration of monovalent copper straightforwardly in amorphous hosts. PMID:26919120

  19. Monitoring Temperature in High Enthalpy Arc-heated Plasma Flows using Tunable Diode Laser Absorption Spectroscopy

    Martin, Marcel Nations; Chang, Leyen S.; Jeffries, Jay B.; Hanson, Ronald K.; Nawaz, Anuscheh; Taunk, Jaswinder S.; Driver, David M.; Raiche, George

    2013-01-01

    A tunable diode laser sensor was designed for in situ monitoring of temperature in the arc heater of the NASA Ames IHF arcjet facility (60 MW). An external cavity diode laser was used to generate light at 777.2 nm and laser absorption used to monitor the population of electronically excited oxygen atoms in an air plasma flow. Under the assumption of thermochemical equilibrium, time-resolved temperature measurements were obtained on four lines-of-sight, which enabled evaluation of the temperature uniformity in the plasma column for different arcjet operating conditions.

  20. X-ray absorption fine structure spectroscopy studies of thiol-capped copper nanoparticles

    Monodisperse Copper nanoparticles with controllable sizes of 0.6 and 1.8nm were synthesized via modifying Brust-Schiffrin two-phase method. This route involves a slow reduction of [TOA]2[CuBr4] precursor in toluene, with particles sizes rationally controlled by the S/Cu ratio. Size-dependent inter-atomic distance contraction in the thiol-capped copper nanoparticles was investigated by Extended X-ray Absorption Fine Structure (EXAFS). The analysis revealed a shortened Cu-Cu inter-atomic distance, indicating strong surface interaction, in accord with the larger effect expected for ultrasmall particals (<2nm).

  1. Time-resolved nonlinear polarization spectroscopy for measuring transient absorption and refraction in isotropic materials

    Taranenko, Victor B.; Bazhenov, Vladimir Y.; Kulikovskaya, Olga A.

    1995-11-01

    A novel time-resolved nonlinear spectroscopic technique is described, which is based on stroboscopic registration of optical polarization transformation taking place at a vector incoherent two-wave mixing interaction in a modified Mach-Zehnder interferometer. It allows an accurate measuring of the dynamics of excitation and relaxation for real and imaginary parts of complex nonlinearity tensor components. The technique is demonstrated for measuring the light-induced change of transient absorption (delta) (alpha) e(t), (delta) (alpha) o(t) and refraction (delta) ne(t), (delta) no(t) for bacteriorhodopsin- based film pumped by linearly polarized laser pulses.

  2. Comparison Between X-rays Absorption and Emission Spectroscopy Measurements on a Ceramic Envelop Lamp

    Bruno LAFITTE; Michel AUBES; Georges ZISSIS

    2007-01-01

    Burners of metal halide lamps used for illumination are generally made of polycrystalline alumina ceramic (PCA) which is translucent to visible light.We show that the difficulty of selecting a line of sight through the lamp prevents the use of optical emission diagnostic.X-rays photons are mainly absorbed and not scattered by PCA.Absorption by mercury atoms contributing to the discharge allowed us to determine the density of mercury in the lamp.By comparing diagnostic methods,we put in evidence the difficulty of taking into account the scattering of light mathematically.

  3. Electron volt spectroscopy on a pulsed neutron source using resonance absorption filters

    The design aspects of an inelastic neutron spectrometer based on energy selection by the resonance absorption filter difference method are discussed. Detailed calculations of the accessible dynamical range (Q, ω), energy and momentum transfer resolutions and representative count rates are presented for Sm and Ta resonance filters in an inverse geometry spectrometer on a high intensity pulsed source such as the RAL Spallation Neutron Source (SNS). A discussion is given of the double-difference method, which provides a means of improving the resonance attenuation peak shape. As a result of this study, as well as preliminary experimental results, recommendations are made for the future development of the technique. (author)

  4. Decay heat and anti-neutrino energy spectra in fission fragments from total absorption spectroscopy

    Rykaczewski, Krzysztof

    2015-10-01

    Decay studies of over forty 238U fission products have been studied using ORNL's Modular Total Absorption Spectrometer. The results are showing increased decay heat values, by 10% to 50%, and the energy spectra of anti-neutrinos shifted towards lower energies. The latter effect is resulting in a reduced number of anti-neutrinos interacting with matter, often by tens of percent per fission product. The results for several studied nuclei will be presented and their impact on decay heat pattern in power reactors and reactor anti-neutrino physics will be discussed.

  5. Symmetry Breaking in Platinum Acetylide Chromophores Studied by Femtosecond Two-Photon Absorption Spectroscopy.

    Rebane, Aleksander; Drobizhev, Mikhail; Makarov, Nikolay S; Wicks, Geoffrey; Wnuk, Pawel; Stepanenko, Yuriy; Haley, Joy E; Krein, Douglas M; Fore, Jennifer L; Burke, Aaron R; Slagle, Jonathan E; McLean, Daniel G; Cooper, Thomas M

    2014-05-15

    We study instantaneous two-photon absorption (2PA) in a series of nominally quasi-centrosymmetric trans-bis(tributylphosphine)-bis-(4-((9,9-diethyl-7-ethynyl-9H-fluoren-2-yl) ethynyl)-R)-platinum complexes, where 11 different substituents, R = N(phenyl)2(NPh2), NH2, OCH3, t-butyl, CH3, H, F, CF3, CN, benzothiazole, and NO2, represent a range of electron-donating (ED) and electron-withdrawing (EW) strengths, while the Pt core acts as a weak ED group. We measure the 2PA cross section in the 540-810 nm excitation wavelength range by complementary femtosecond two-photon excited fluorescence (2PEF) and nonlinear transmission (NLT) methods and compare the obtained values to those of the Pt-core chromophore and the corresponding noncentrosymmetric side group (ligand) chromophores. Peak 2PA cross sections of neutral and ED-substituted Pt complexes occur at S0 → Sn transitions to higher energy states, above the lowest-energy S0 → S1 transition, and the corresponding values increase systematically with increasing ED strength, reaching maximum value, σ2 ∼ 300 GM (1 GM = 10(-50) cm(4) s), for R = NPh2. At transition energies overlapping with the lowest-energy S0 → S1 transition in the one-photon absorption (1PA) spectrum, the same neutral and ED-substituted Pt complexes show weak 2PA, σ2 NO2, while in the S0 → Sn transition region the peak 2PEF cross section decreases. We explained this effect by breaking of inversion symmetry due to conformational distortions associated with low energy barrier for ground-state rotation of the ligands. Our findings are corroborated by theoretical calculations that show large increase of the permanent electric dipole moment change in the S0 → S1 transition when ligands with strong EW substituents are twisted by 90° relative to the planar chromophore. Our NLT results in the S0 → S1 transition region are quantitatively similar to those obtained from the 2PEF measurement. However, at higher transition energy corresponding to S0

  6. Atomic structure of Mn-rich nanocolumns probed by x-ray absorption spectroscopy

    Rovezzi, M.; Devillers, T.; Arras, E.; d'Acapito, F.; Barski, A.; Jamet, M.; Pochet, P.

    2008-06-01

    In this letter, we have used the extended x-ray-absorption fine-structure (EXAFS) technique to investigate the structure of Mn-rich self-organized nanocolumns grown by low temperature molecular beam epitaxy. The EXAFS analysis has shown that Mn-rich nanocolumns exhibit a complex local structure that cannot be described by a simple substitutional model. Additional interatomic distances had to be considered in the EXAFS model which are in excellent agreement with the structure of a Ge-3Mn building block tetrahedron of Ge3Mn5.

  7. Measurements of liquid film thickness, concentration, and temperature of aqueous urea solution by NIR absorption spectroscopy

    Pan, R.; Jeffries, J. B.; Dreier, T.; Schulz, C.

    2016-01-01

    A multi-wavelength near-infrared (NIR) diode laser absorption sensor has been developed and demonstrated for real-time monitoring of the thickness, solute concentration, and temperature of thin films of urea-water solutions. The sensor monitors the transmittance of three near-infrared diode lasers through the thin liquid film. Film thickness, urea mass fraction, and liquid temperature were determined from measured transmittance ratios of suitable combinations of lasers. Available laser wavelengths were selected depending on the variation of the NIR absorption spectrum of the solution with temperature and solute concentration. The spectral database was measured by a Fourier transform infrared spectrometer in the range 5500-8000 cm-1 for urea solutions between 5 and 40 wt% and temperatures between 298 and 338 K. A prototype sensor was constructed, and the sensor concept was first validated with measurements using a calibration cell providing liquid layers of variable thickness (200-1500 µm), urea mass fraction (5-40 wt%) and temperature (298-318 K). Temporal variations of film thickness and urea concentration were captured during the constant-temperature evaporation of a liquid film deposited on an optically polished heated quartz flat.

  8. Binding of anti-prion agents to glycosaminoglycans: Evidence from electronic absorption and circular dichroism spectroscopy

    The polyanionic glycosaminoglycans (GAGs) are intimately involved in the pathogenesis of protein conformational disorders such as amyloidosis and prion diseases. Several cationic agents are known to exhibit anti-prion activity but their mechanism of action is poorly understood. In this study, UV absorption and circular dichroism (CD) spectroscopic techniques were used to investigate the interaction between heparin and chondroitin-6-sulfate and anti-prion drugs including acridine, quinoline, and phenothiazine derivatives. UV band hypochromism of (±)-quinacrine, (±)-primaquine, tacrine, quinidine, chlorpromazine, and induced CD spectra of (±)-quinacrine upon addition of GAGs provided evidence for the GAG binding of these compounds. The association constants (∼106-107 M-1) estimated from the UV titration curves show high-affinity drug-heparin interactions. Ionic strength-dependence of the absorption spectra suggested that the interaction between GAGs and the cationic drugs is principally electrostatic in nature. Drug binding differences of heparin and chondroitin-6-sulfate were attributed to their different negative charge density. These results call the attention to the alteration of GAG-prion/GAG-amyloid interactions by which these compounds might exert their anti-prion/anti-amyloidogenic activities

  9. Electronic structure of barium strontium titanate by soft-x-ray absorption spectroscopy

    Uehara, Y. [Mitsubishi Electric Co., Hyogo (Japan); Underwood, J.H.; Gullikson, E.M.; Perera, R.C.C. [Ernest Orlando Lawrence Berkeley National Lab., CA (United States)

    1997-04-01

    Perovskite-type titanates, such as Strontium Titanate (STO), Barium Titanate (BTO), and Lead Titanate (PTO) have been widely studied because they show good electric and optical properties. In recent years, thin films of Barium Strontium Titanate (BST) have been paid much attention as dielectrics of dynamic random access memory (DRAM) capacitors. BST is a better insulator with a higher dielectric constant than STO and can be controlled in a paraelectric phase with an appropriate ratio of Ba/Sr composition, however, few studies have been done on the electronic structure of the material. Studies of the electronic structure of such materials can be beneficial, both for fundamental physics research and for improving technological applications. BTO is a famous ferroelectric material with a tetragonal structure, in which Ti and Ba atoms are slightly displaced from the lattice points. On the other hand, BST keeps a paraelectric phase, which means that the atoms are still at the cubic lattice points. It should be of great interest to see how this difference of the local structure around Ti atoms between BTO and BST effects the electronic structure of these two materials. In this report, the authors present the Ti L{sub 2,3} absorption spectra of STO, BTO, and BST measured with very high accuracy in energy of the absorption features.

  10. X-ray absorption spectroscopy and imaging of heterogeneous hydrothermal mixtures using a diamond microreactor cell

    Hydrothermal synthesis is an important route to novel materials. Hydrothermal chemistry is also an important aspect of geochemistry and a variety of waste remediation technologies. There is a significant lack of information about the speciation of inorganic compounds under hydrothermal conditions. For these reasons we describe a high-temperature, high-pressure cell that allows one to acquire both x-ray absorption fine structure (XAFS) spectra and x-ray transmission and absorption images of heterogeneous hydrothermal mixtures. We demonstrate the utility of the method by measuring the Cu(I) speciation in a solution containing both solid and dissolved Cu phases at temperatures up to 325oC. X-ray imaging of the various hydrothermal phases allows micro-XAFS to be collected from different phases within the heterogeneous mixture. The complete structural characterization of a soluble bichloro-cuprous species was determined. In situ XAFS measurements were used to define the oxidation state and the first-shell coordination structure. The Cu--Cl distance was determined to be 2.12 Aa for the CuCl2- species and the complete loss of tightly bound waters of hydration in the first shell was observed. The microreactor cell described here can be used to test thermodynamic models of solubility and redox chemistry of a variety of different hydrothermal mixtures

  11. Relaxation dynamics in the excited states of a ketocyanine dye probed by femtosecond transient absorption spectroscopy

    Jahur A Mondal; Sandeep Verma; Hirendra N Ghosh; Dipak K Palit

    2008-01-01

    Relaxation dynamics of the excited singlet states of 2,5-bis-(N-methyl-N-1,3-propdienylaniline)-cyclopentanone (MPAC), a ketocyanine dye, have been investigated using steady-state absorption and emission as well as femtosecond time-resolved absorption spectroscopic techniques. Following photoexcitation using 400 nm light, the molecule is excited to the S2 state, which is fluorescent in rigid matrices at 77 K. S2 state is nearly non-fluorescent in solution and has a very short lifetime (0.5 ± 0.2 ps). In polar aprotic solvents, the S1 state follows a complex multi-exponential relaxation dynamics consisting of torsional motion of the donor groups, solvent re-organization as well as photoisomerization processes. However, in alcoholic solvents, solvent re-organization via intermolecular hydrogen-bonding interaction is the only relaxation process observed in the S1 state. In trifluoroethanol, a strong hydrogen bonding solvent, conversion of the non-hydrogen-bonded form, which is formed following photoexcitation, to the hydrogen-bonded complex has been clearly evident in the relaxation process of the S1 state.

  12. Double conical crystal x-ray spectrometer for high resolution ultrafast x-ray absorption near-edge spectroscopy of Al K edge

    Levy, A.; Dorchies, F.; Fourment, C.; Harmand, M.; Hulin, S.; Santos, J. J.; Descamps, D.; Petit, S.; Bouillaud, R. [Centre Lasers Intenses et Applications (CELIA), Universite de Bordeaux-CNRS-CEA, Talence F-33405 (France)

    2010-06-15

    An x-ray spectrometer devoted to dynamical studies of transient systems using the x-ray absorption fine spectroscopy technique is presented in this article. Using an ultrafast laser-induced x-ray source, this optical device based on a set of two potassium acid phthalate conical crystals allows the extraction of x-ray absorption near-edge spectroscopy structures following the Al absorption K edge. The proposed experimental protocol leads to a measurement of the absorption spectra free from any crystal reflectivity defaults and shot-to-shot x-ray spectral fluctuation. According to the detailed analysis of the experimental results, a spectral resolution of 0.7 eV rms and relative fluctuation lower than 1% rms are achieved, demonstrated to be limited by the statistics of photon counting on the x-ray detector.

  13. Chiral-index resolved length mapping of carbon nanotubes in solution using electric-field induced differential absorption spectroscopy

    Li, Wenshan; Hennrich, Frank; Flavel, Benjamin S.; Kappes, Manfred M.; Krupke, Ralph

    2016-09-01

    The length of single-walled carbon nanotubes (SWCNTs) is an important metric for the integration of SWCNTs into devices and for the performance of SWCNT-based electronic or optoelectronic applications. In this work we propose a rather simple method based on electric-field induced differential absorption spectroscopy to measure the chiral-index-resolved average length of SWCNTs in dispersions. The method takes advantage of the electric-field induced length-dependent dipole moment of nanotubes and has been verified and calibrated by atomic force microscopy. This method not only provides a low cost, in situ approach for length measurements of SWCNTs in dispersion, but due to the sensitivity of the method to the SWCNT chiral index, the chiral index dependent average length of fractions obtained by chromatographic sorting can also be derived. Also, the determination of the chiral-index resolved length distribution seems to be possible using this method.

  14. Fixed-wavelength H2O absorption spectroscopy system enhanced by an on-board external-cavity diode laser

    Brittelle, Mack S.; Simms, Jean M.; Sanders, Scott T.; Gord, James R.; Roy, Sukesh

    2016-03-01

    We describe a system designed to perform fixed-wavelength absorption spectroscopy of H2O vapor in practical combustion devices. The system includes seven wavelength-stabilized distributed feedback (WSDFB) lasers, each with a spectral accuracy of  ±1 MHz. An on-board external cavity diode laser (ECDL) that tunes 1320-1365 nm extends the capabilities of the system. Five system operation modes are described. In one mode, a sweep of the ECDL is used to monitor each WSDFB laser wavelength with an accuracy of  ±30 MHz. Demonstrations of fixed-wavelength thermometry at 10 kHz bandwidth in near-room-temperature gases are presented; one test reveals a temperature measurement error of ~0.43%.

  15. Self-corrected sensors based on atomic absorption spectroscopy for atom flux measurements in molecular beam epitaxy

    A high sensitivity atom flux sensor based on atomic absorption spectroscopy has been designed and implemented to control electron beam evaporators and effusion cells in a molecular beam epitaxy system. Using a high-resolution spectrometer and a two-dimensional charge coupled device detector in a double-beam configuration, we employ either a non-resonant line or a resonant line with low cross section from the same hollow cathode lamp as the reference for nearly perfect background correction and baseline drift removal. This setup also significantly shortens the warm-up time needed compared to other sensor technologies and drastically reduces the noise coming from the surrounding environment. In addition, the high-resolution spectrometer allows the most sensitive resonant line to be isolated and used to provide excellent signal-to-noise ratio

  16. An in situ and operando X-ray absorption spectroscopy setup for measuring sub-monolayer model and powder catalysts.

    Weiher, Norbert; Bus, Eveline; Gorzolnik, Blazej; Möller, Martin; Prins, Roel; van Bokhoven, Jeroen Anton

    2005-09-01

    A new spectroscopic cell has been designed for studying model catalysts using in situ or operando X-ray absorption spectroscopy. The setup allows gas treatment and can be used between 100 and 870 K. Pressures from 10(-3) Pa up to 300 kPa can be applied. Measurements on model systems in this particular pressure range are a valuable extension of the commonly used UHV characterization techniques. Using this setup, we were able to analyze the Au L3 EXAFS of a silica wafer covered with sub-monolayer concentrations of gold (0.05 ML). By modifying the sample holder, powder catalysts can also be analyzed under plug-flow conditions. As an example, the reduction of a Au/SiO2 powder catalyst prepared from HAuCl4 was followed. PMID:16120994

  17. Diagnostics of reactive pulsed plasmas by UV and VUV absorption spectroscopy and by modulated beam Mass spectrometry

    Cunge, Gilles

    2011-10-01

    Pulsed plasmas are promising for etching applications in the microelectronic industry. However, many new phenomena are involved when a high density discharge is pulsed. To better understand these processes it is necessary to probe the radicals' kinetics with a microsecond resolution. We have developed several diagnostics to reach this goal including broad band absorption spectroscopy with UV LEDs to detect small polyatomic radicals and with a deuterium VUV source to detect larger closed shell molecules and the modulated mass spectrometry to monitor atomic species. We will discuss the impact of the plasma pulsing frequency and duty cycle on the radical densities in Cl2 based plasmas, and the consequences on plasma processes. Work done in collaboration with Paul Bodart, Melisa Brihoum, Maxime Darnon, Erwin Pargon, Olivier Joubert, and Nader Sadeghi, CNRS/LTM.

  18. Application of Polarization Modulated Infrared Reflection Absorption Spectroscopy for electrocatalytic activity studies of laccase adsorbed on modified gold electrodes

    Orientation of the enzyme macromolecule on the electrode surface is crucially important for the efficiency of the electron transport between the active site and electrode surface. The orientation can be controlled by affecting the surface charge and the pH of the buffer solution. In this contribution we study laccase physically adsorbed on gold surface modified by mercapto-ethanol, lipid and variously charged diazonium salts. Polarization Modulated Infrared Reflection Absorption Spectroscopy (PMIRRAS) enables the molecular orientation study of the protein molecule by comparison of the amide I to amide II band intensity ratios assuming that the protein secondary structure does not change. We observe significant differences in the intensity ratios depending on the kind of support and the enzyme deposition. The comparison of infrared spectra and cyclic voltammetry responses of variously prepared laccase layers reveals that the parallel orientation of beta-sheet moieties results in high enzyme activity

  19. Fixed-wavelength H2O absorption spectroscopy system enhanced by an on-board external-cavity diode laser

    We describe a system designed to perform fixed-wavelength absorption spectroscopy of H2O vapor in practical combustion devices. The system includes seven wavelength-stabilized distributed feedback (WSDFB) lasers, each with a spectral accuracy of  ±1 MHz. An on-board external cavity diode laser (ECDL) that tunes 1320–1365 nm extends the capabilities of the system. Five system operation modes are described. In one mode, a sweep of the ECDL is used to monitor each WSDFB laser wavelength with an accuracy of  ±30 MHz. Demonstrations of fixed-wavelength thermometry at 10 kHz bandwidth in near-room-temperature gases are presented; one test reveals a temperature measurement error of ∼0.43%. (paper)

  20. 3D-printed photo-spectroelectrochemical devices for in situ and in operando X-ray absorption spectroscopy investigation.

    Achilli, Elisabetta; Minguzzi, Alessandro; Visibile, Alberto; Locatelli, Cristina; Vertova, Alberto; Naldoni, Alberto; Rondinini, Sandra; Auricchio, Ferdinando; Marconi, Stefania; Fracchia, Martina; Ghigna, Paolo

    2016-03-01

    Three-dimensional printed multi-purpose electrochemical devices for X-ray absorption spectroscopy are presented in this paper. The aim of this work is to show how three-dimensional printing can be a strategy for the creation of electrochemical cells for in situ and in operando experiments by means of synchrotron radiation. As a case study, the description of two cells which have been employed in experiments on photoanodes for photoelectrochemical water splitting are presented. The main advantages of these electrochemical devices are associated with their compactness and with the precision of the three-dimensional printing systems which allows details to be obtained that would otherwise be difficult. Thanks to these systems it was possible to combine synchrotron-based methods with complementary techniques in order to study the mechanism of the photoelectrocatalytic process. PMID:26917152

  1. Interaction of plasma-generated water cluster ions with chemically-modified Si surfaces investigated by infrared absorption spectroscopy

    Ayumi Hirano-Iwata

    2016-03-01

    Full Text Available We have investigated the interaction of water cluster ions generated by discharge plasma, with chemically modified Si surfaces using infrared absorption spectroscopy in the multiple internal reflection geometry. We observe that water cluster ions readily adsorb on SiO2-covered Si surfaces to form water droplets. We demonstrate that positively- and negatively-charged cluster ions adsorb on the SiO2-covered Si surface in different manners, indicating ionic interaction of the water droplets with the negatively-charged SiO2 surface. Water droplets formed on the protein-coated surface rupture the amide bond of the proteins, suggesting the function of protein decomposition of water cluster ions.

  2. Molecular ordering effect of regioregular poly(3-hexylthiophene) using sulfur K-edge X-ray absorption spectroscopy

    The electronic structure of the unoccupied conduction band of regioregular poly(3-hexylthiophene) (RR-P3HT) was investigated by X-ray absorption spectroscopy (XAS) near the sulfur K-edge. Angle-dependent XAS studies revealed that polymer chains in films are well aligned and oriented edge-on with respect to the Si substrate. It was clearly observed that the bottom of the conduction band near the Fermi level in a π-π stacking film is lower (0.3 eV) than that in a powder. It was demonstrated that π-π stacking interactions improve the power conversion efficiency through the reduction of the lowest unoccupied molecular orbital (LUMO) energy level. (author)

  3. Experimental station for laser-based picosecond time-resolved x-ray absorption near-edge spectroscopy

    We present an experimental station designed for time-resolved X-ray Absorption Near-Edge Spectroscopy (XANES). It is based on ultrashort laser-plasma x-ray pulses generated from a table-top 100 mJ-class laser at 10 Hz repetition rate. A high transmission (10%–20%) x-ray beam line transport using polycapillary optics allows us to set the sample in an independent vacuum chamber, providing high flexibility over a wide spectral range from 0.5 up to 4 keV. Some XANES spectra are presented, demonstrating 1% noise level in only ∼1 mn and ∼100 cumulated laser shots. Time-resolved measurements are reported, indicating that the time resolution of the entire experimental station is 3.3 ± 0.6 ps rms

  4. Electrooxidation of ethanol on Pt and PtRu surfaces investigated by ATR surface-enhanced infrared absorption spectroscopy

    Silva, Marcio F.; Camara, Giuseppe A., E-mail: giuseppe.silva@ufms.br [Departamento de Quimica, Universidade Federal do Mato Grosso do Sul, Campo Grande-MS (Brazil); Batista, Bruno C.; Boscheto, Emerson [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, Sao Carlos-SP, (Brazil); Varela, Hamilton, E-mail: varela@iqsc.usp.br [Ertl Center for Electrochemistry and Catalysis, Gwangju Institute of Science and Technology (GIST), Gwangju (Korea, Republic of)

    2012-05-15

    Herein, it was investigated for the first time the electro-oxidation of ethanol on Pt and PtRu electrodeposits in acidic media by using in situ surface enhanced infrared absorption spectroscopy with attenuated total reflection (ATR-SEIRAS). The experimental setup circumvents the weak absorbance signals related to adsorbed species, usually observed for rough, electrodeposited surfaces, and allows a full description of the CO coverage with the potential for both catalysts. The dynamics of adsorption-oxidation of CO was accessed by ATR-SEIRAS experiments (involving four ethanol concentrations) and correlated with expressions derived from a simple kinetic model. Kinetic analysis suggests that the growing of the CO adsorbed layer is nor influenced by the presence of Ru neither by the concentration of ethanol. The results suggest that the C-C scission is not related to the presence of Ru and probably happens at Pt sites. (author)

  5. Some investigation on trace elements content of Iranian breads using neutron activation analysis and atomic absorption spectroscopy

    Since bread is consumed as a principal dietary staple by the majority of Iranian communities, actual natural portion of required protein and energy are provided via bread. Therefore, with respect to this matter, a considerable amount of needed minerals must also be met through this way. Literature survey indicates some elemental deficiencies as the result of consumption of bread in Iran. On the other hand, essentiality of these elements to human which are mostly in the range of trace amounts, makes this investigation very much important and interesting from both sides, nutritionally and instrumentally. To meet the above requirements, applications of very sensitive analytical tools are unavoidable. Hence, atomic absorption spectroscopy and neutron activation analysis both RNAA and INAA are employed. Results are controversial and constructive

  6. Hot Carrier Dynamics in the X Valley in Si and Ge Measured by Pump-IR-Probe Absorption Spectroscopy

    Wang, W. B.; Cavicchia, M. A.; Alfano, R. R.

    1996-01-01

    Si is the semiconductor of choice for nanoelectronic roadmap into the next century for computer and other nanodevices. With growing interest in Si, Ge, and Si(sub m)Ge(sub n) strained superlattices, knowledge of the carrier relaxation processes in these materials and structures has become increasingly important. The limited time resolution for earlier studies of carrier dynamics in Ge and Si, performed using Nd:glass lasers, was not sufficient to observe the fast cooling processes. In this paper, we present a direct measurement of hot carrier dynamics in the satellite X valley in Si and Ge by time-resolved infrared(IR) absorption spectroscopy, and show the potential of our technique to identify whether the X valley is the lowest conduction valley in semiconductor materials and structures.

  7. [Measurement of atmospheric NO3 radical with long path differential optical absorption spectroscopy based on red light emitting diodes].

    Li, Su-Wen; Liu, Wen-Qing; Wang, Jiang-Tao; Xie, Pin-Hua; Wang, Xu-De

    2013-02-01

    Nitrate radical (NO3) is the most important oxidant in the tropospheric nighttime chemistry. Due to its high reactivity and low atmospheric concentrations, modern red light emitting diodes (LEDs) was proposed as light source in long path differential optical absorption spectroscopy (LP-DOAS) to measure NO3 radical in the atmosphere. The spectral properties of Luxeon LXHL-MD1D LEDs were analyzed in the present paper. The principle of LEDs-DOAS system to measure nitrate radical was studied in this paper. The experimental setup and retrieval method of NO3 radical were discussed in this paper. The retrieved example of NO3 was given and the time series of NO3 concentrations was performed for a week. The results showed that the detection limits of LEDs-DOAS system were 12 ppt for atmospheric NO3 radical when the optical path of LEDs-DOAS system was 2.8 km. PMID:23697129

  8. Spatially resolved measurements of nitrogen dioxide in an urban environment using concurrent multi-axis differential optical absorption spectroscopy

    R. J. Leigh

    2006-12-01

    Full Text Available A novel system using the technique of concurrent multi-axis differential optical absorption spectroscopy system has been developed and applied to the measurement of nitrogen dioxide in an urban environment. Using five fixed telescopes, slant columns of nitrogen dioxide, ozone, water vapour, and the oxygen dimer, O4, are simultaneously retrieved in five vertically separated viewing directions. The application of this remote sensing technique in the urban environment is explored. Through, the application of several simplifying assumptions a tropospheric concentration of NO2 is derived and compared with an urban background in-situ chemiluminescence detector. The remote sensing and in-situ techniques show good agreement. Owing to the high time resolution of the measurements, the ability to image and quantify plumes within the urban environment is demonstrated. The CMAX-DOAS measurements provide a useful measure of overall NO2 concentrations on a city-wide scale.

  9. Low-cost, heated, and/or cooled flow-through cell for transmission x-ray absorption spectroscopy

    Jentoft, R. E.; Deutsch, S. E.; Gates, B. C.

    1996-06-01

    A transmission x-ray absorption spectroscopy cell that can be used for air-sensitive samples with in situ treatment is described. The cell is designed with a relatively small size for use with air-sensitive powdered catalyst samples that must be loaded in a glove box. Samples can be treated in situ with gas flow or vacuum and temperature control up to 500 °C. The cell is constructed of stainless steel and designed for durability as well as ease of repair. The cells are vacuum tight and equipped with beryllium windows sealed with vacuum O-ring flanges for easy loading. Each cell, with all parts excluding the windows, costs about 2700.

  10. Electrochemical discharge of nanocrystalline magnetite: structure analysis using X-ray diffraction and X-ray absorption spectroscopy.

    Menard, Melissa C; Takeuchi, Kenneth J; Marschilok, Amy C; Takeuchi, Esther S

    2013-11-14

    Magnetite (Fe3O4) is an abundant, low cost, environmentally benign material with potential application in batteries. Recently, low temperature coprecipitation methods have enabled preparation of a series of nanocrystalline magnetite samples with a range of crystallite sizes. Electrochemical cells based on Li/Fe3O4 show a linear increase in capacity with decreasing crystallite size at voltages ≥1.2 V where a 2× capacity improvement relative to commercial (26.2 nm) magnetite is observed. In this report, a combination of X-ray powder diffraction (XRD) and X-ray absorption spectroscopy (XAS) is used to measure magnetite structural changes occurring upon electrochemical reduction, with parent Fe3O4 crystallite size as a variable. Notably, XAS provides evidence of metallic iron formation at high levels of electrochemical reduction. PMID:24077019

  11. Investigation of the structure and chemistry of surface layers on metals by x-ray absorption spectroscopy

    Most structural metals are very active chemically and without a passivating or protective layer would soon oxidize or corrode. The history of the industry is an attempt to minimize this process. The problem is becoming more acute, particularly in the aerospace industry, where the frames of many older airplanes are lasting longer than their outer skins. A more esoteric effect is the corrosion of metal surfaces in earth orbit by atomic oxygen. This paper is concerned with the structural and chemical characterization by x-ray absorption spectroscopy (XAS) of surface layers on aluminum alloys exposed to salt spray testing and with iron-based A-286 superalloy bolts exposed to atomic oxygen in a low earth orbit

  12. Multibeam long-path differential optical absorption spectroscopy instrument: a device for simultaneous measurements along multiple light paths.

    Pundt, Irene; Mettendorf, Kai Uwe

    2005-08-10

    A novel long-path differential optical absorption spectroscopy (DOAS) apparatus for measuring tropospheric trace gases and the first results from its use are presented: We call it the multibeam instrument. It is the first active DOAS device that emits several light beams simultaneously through only one telescope and with only one lamp as a light source, allowing simultaneous measurement along multiple light paths. In contrast to conventional DOAS instruments, several small mirrors are positioned near the lamp, creating multiple virtual light sources that emit one light beam each in one specific direction. The possibility of error due to scattering between the light beams is negligible. The trace-gas detection limits of NO2, SO2, O3, and H2CO are similar to those of the traditional long-path DOAS instrument. PMID:16114540

  13. Measurement of free radical kinetics in pulsed plasmas by UV and VUV absorption spectroscopy and by modulated beam mass spectrometry

    This paper reviews recent progress in the development of time-resolved diagnostics to probe high-density pulsed plasma sources. We focus on time-resolved measurements of radicals' densities in the afterglow of pulsed discharges to provide useful information on production and loss mechanisms of free radicals. We show that broad-band absorption spectroscopy in the ultraviolet and vacuum ultraviolet spectral domain and threshold ionization modulated beam mass spectrometry are powerful techniques for the determination of the time variation of the radicals' densities in pulsed plasmas. The combination of these complementary techniques allows detection of most of the reactive species present in industrial etching plasmas, giving insights into the physico-chemistry reactions involving these species. As an example, we discuss briefly the radicals' kinetics in the afterglow of a SiCl4/Cl2/Ar discharge. (paper)

  14. In situ time-resolved X-ray near-edge absorption spectroscopy of selenite reduction by siderite

    The reduction oxidation-reaction between aqueous selenite (SeO32-) and siderite (FeCO3(s)) was monitored by in situ, time-resolved X-ray absorption near-edge structure (XANES) spectroscopy at the selenium K edge in a controlled electrochemical environment. Spectral evolutions showed that more than 60% of selenite was reduced at the siderite surface after 20 h of experiment, at which time the reaction was still incomplete. Fitting of XANES spectra by linear combination of reference spectra showed that selenite reaction with siderite is essentially a two-step process, selenite ions being immobilized on siderite surface prior to their reduction. A kinetic model of the reduction step is proposed, allowing to identify the specific contribution of surface reduction. These results have strong implications for the retention of selenite by corrosion products in nuclear waste repositories and in a larger extent for the fate of selenium in the environment. (authors)

  15. Detection Limit of Glucose Concentration with Near-Infrared Absorption and Scattering Spectroscopy

    LUO Yun-Han; HUANG Fu-Rong; LI Shi-Ping; CHEN Zhe

    2008-01-01

    @@ Theoretical analyses and Monte Carlo simulation are performed to investigate the detection limit of glucose concentration with near-infrared spectroscopy.The relation between detection limitation of glucose concentration and source-detector separation is derived.Monte Carlo simulation performed with a skin-layered model shows that the ratio of effective photons from the target layer could excess 50% by selecting proper source-detector separation,and that the detection limit of glucose concentration approaches to 0.28mM,which satisfies the requirement of food and drug administration for noninvasive glucose sensing.

  16. In-situ X-Ray Absorption Spectroscopy (XAS) Investigation of a Bifunctional Manganese Oxide Catalyst with High Activity for Electrochemical Water Oxidation and Oxygen Reduction

    Gorlin, Yelena; Lassalle-Kaiser, Benedikt; Benck, Jesse D.; Gul, Sheraz; Webb, Samuel M; Yachandra, Vittal K.; Yano, Junko; Jaramillo, Thomas F.

    2013-01-01

    In-situ x-ray absorption spectroscopy (XAS) is a powerful technique that can be applied to electrochemical systems, with the ability to elucidate the chemical nature of electrocatalysts under reaction conditions. In this study, we perform in-situ XAS measurements on a bifunctional manganese oxide (MnOx) catalyst with high electrochemical activity for the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER). Using x-ray absorption near edge structure (XANES) and extended x-r...

  17. Incorporation of Trace Elements in Ancient and Modern Human Bone: An X-Ray Absorption Spectroscopy Study

    Pingitore, N. E.; Cruz-Jimenez, G.; Price, T. D.

    2001-12-01

    X-ray absorption spectroscopy (XAS) affords the opportunity to probe the atomic environment of trace elements in human bone. We are using XAS to investigate the mode(s) of incorporation of Sr, Zn, Pb, and Ba in both modern and ancient (and thus possibly altered) human and animal bone. Because burial and diagenesis may add trace elements to bone, we performed XAS analysis on samples of pristine contemporary and ancient, buried human and animal bone. We assume that deposition of these elements during burial occurs by processes distinct from those in vivo, and this will be reflected in their atomic environments. Archaeologists measure strontium in human and animal bone as a guide to diet. Carnivores show lower Sr/Ca ratios than their herbivore prey due to discrimination against Sr relative to Ca up the food chain. In an initial sample suite no difference was observed between modern and buried bone. Analysis of additional buried samples, using a more sensitive detector, revealed significant differences in the distance to the second and third neighbors of the Sr in some of the buried samples. Distances to the first neighbor, oxygen, were similar in all samples. Zinc is also used in paleo-diet studies. Initial x-ray absorption spectroscopy of a limited suite of bones did not reveal any differences between modern and buried samples. This may reflect the limited number of samples examined or the low levels of Zn in typical aqueous solutions in soils. Signals from barium and lead were too low to record useful XAS spectra. Additional samples will be studied for Zn, Ba, and Pb. We conducted our XAS experiments on beam lines 4-1 and 4-3 at the Stanford Synchrotron Radiation Laboratory. Data were collected in the fluorescence mode, using a Lytle detector and appropriate filter, and a solid state, 13-element Ge-detector.

  18. Post-discharge gas composition of a large-gap DBD in humid air by UV–Vis absorption spectroscopy

    Large gap dielectric barrier discharges (DBD) provide non-thermal, non-equilibrium plasmas that can generate specific gas chemistry with enhanced bactericidal effects when working in humid air. The present study investigates the post-discharge gas composition of such plasmas operated in humid air using UV–Vis (200–800 nm) absorption spectroscopy. Absorbance spectra have been de-convoluted using direct deconvolution and iterative methods and results are correlated to the DBD electrical parameters. The high-voltage (56 and 70 kV rms) DBD plasma generated at 50 Hz frequency in a closed container over a 20 mm gap in air with relative humidity (RH) of 5–70% has been characterized by I–V and capacitive methods. The post-discharge gas composition at each RH is assessed by UV–Vis absorption spectroscopy for plasma exposure times of 15–120 s. The concentration of ozone and nitrogen oxides (O3, NO2, NO3, N2O4) increases with plasma exposure time but a strong decrease in [O3] levels is obtained with increase in RH. The decrease in [O3] and an abundance of nitrogen oxides is ascribed to high specific power densities in the closed container and to increasing RH levels. The absorbance residual following deconvolution shows a strong band at 230–270 nm consistent with the presence of pernitric acid (HNO4) and other HNOx (x = 1, 3) species. Humid air large gap DBD plasmas in closed containers generate along with O3, high levels of nitrogen oxides and HNOx (x = 1, 4) acids leading to increased bactericidal rates. (paper)

  19. X-ray absorption spectroscopy of hemes and hemeproteins in solution: multiple scattering analysis.

    D'Angelo, Paola; Lapi, Andrea; Migliorati, Valentina; Arcovito, Alessandro; Benfatto, Maurizio; Roscioni, Otello Maria; Meyer-Klaucke, Wolfram; Della-Longa, Stefano

    2008-11-01

    A full quantitative analysis of Fe K-edge X-ray absorption spectra has been performed for hemes in two porphynato complexes, that is, iron(III) tetraphenylporphyrin chloride (Fe(III)TPPCl) and iron(III) tetraphenylporphyrin bis(imidazole) (Fe(III)TPP(Imid)2), in two protein complexes whose X-ray structure is known at atomic resolution (1.0 A), that is, ferrous deoxy-myoglobin (Fe(II)Mb) and ferric aquo-myoglobin (Fe(III)MbH2O), and in ferric cyano-myoglobin (Fe(III)MbCN), whose X-ray structure is known at lower resolution (1.4 A). The analysis has been performed via the multiple scattering approach, starting from a muffin tin approximation of the molecular potential. The Fe-heme structure has been obtained by analyzing independently the Extended X-ray Absorption Fine Structure (EXAFS) region and the X-ray Absorption Near Edge Structure (XANES) region. The EXAFS structural results are in full agreement with the crystallographic values of the models, with an accuracy of +/- 0.02 A for Fe-ligand distances, and +/-6 degrees for angular parameters. All the XANES features above the theoretical zero energy (in the lower rising edge) are well accounted for by single-channel calculations, for both Fe(II) and Fe(III) hemes, and the Fe-N p distance is determined with the same accuracy as EXAFS. XANES evaluations of Fe-5th and Fe-6th ligand distances are determined with 0.04-0.07 A accuracy; a small discrepancy with EXAFS (0.01 to 0.05 A beyond the statistical error), is found for protein compounds. Concerns from statistical correlation among parameters and multiple minima in the parameter space are discussed. As expected, the XANES accuracy is slightly lower than what was found for polarized XANES on Fe(III)MbCN single crystal (0.03-0.04 A), and states the actual state-of-the-art of XANES analysis when used to extract heme-normal parameters in a solution spectrum dominated by heme-plane scattering. PMID:18837548

  20. Effective utilization of quantum-cascade distributed-feedback lasers in absorption spectroscopy

    Kosterev, A. A.; Curl, R. F.; Tittel, F. K.; Gmachl, C.; Capasso, F.; Sivco, D. L.; Baillargeon, J. N.; Hutchinson, A. L.; Cho, A. Y.

    2000-01-01

    A variable duty cycle quasi-cw frequency scanning technique was applied to reduce thermal effects resulting from the high heat dissipation of type I quantum-cascade lasers. This technique was combined with a 100-m path-length multipass cell and a zero-air background-subtraction technique to enhance detection sensitivity to a parts-in-10(9) (ppb) concentration level for spectroscopic trace-gas detection of CH4, N2O, H2O, and C2H5OH in ambient air at 7.9 micrometers. A new technique for analysis of dense high resolution absorption spectra was applied to detection of ethanol in ambient air, yielding a 125-ppb detection limit.

  1. Estimation of lead and cadmium in various food commodities by electrothermal atomic absorption spectroscopy

    The determination of lead and cadmium was carried out in various types of food commodities including poultry farm chicken eggs, integrated diet of winter season for the inhabitants of Rawalpindi/Islamabad area and different brands of baby cereals, employing electrothermal atomic absorption spectrophotometric technique. The results showed that integrated diet contained the highest amount of lead whereas the maximum concentration of cadmium was observed in samples of baby cereals. The effect of mechanical food processing on the concentration levels of these elements was discussed. The results obtained were compared with the reported values for other countries. Intake values of these toxic elements through these food articles were calculated and compared with the tolerance levels of WHO. (author)

  2. Exceptionally strong correlation-driven charge migration and attosecond transient absorption spectroscopy

    Hollstein, Maximilian; Pfannkuche, Daniela

    2016-01-01

    We investigate theoretically charge migration following prompt double ionization of a polyatomic molecule (C$_2$H$_4$BrI) and find that for double ionization, correlation-driven charge migration appears to be particularly prominent, i.e., we observe exceptionally rich dynamics solely driven by the electron-electron interaction even in the situation when the electrons are emitted from outer-valence orbitals. These strongly correlated electron dynamics are witnessed in the theoretically determined time-resolved transient absorption cross section. Strikingly, features in the cross section can be traced back to electron hole populations and time-dependent partial charges and hence, can be interpreted with surprising ease. Remarkably, by taking advantage of element specific core-to-valence transitions, the hole population dynamics can be followed both in time and space. With this, not only do we report the high relevance of correlation-driven charge migration following double ionization but our findings also highl...

  3. UV-vis absorption spectroscopy and multivariate analysis as a method to discriminate tequila

    Barbosa-García, O.; Ramos-Ortíz, G.; Maldonado, J. L.; Pichardo-Molina, J. L.; Meneses-Nava, M. A.; Landgrave, J. E. A.; Cervantes-Martínez, J.

    2007-01-01

    Based on the UV-vis absorption spectra of commercially bottled tequilas, and with the aid of multivariate analysis, it is proved that different brands of white tequila can be identified from such spectra, and that 100% agave and mixed tequilas can be discriminated as well. Our study was done with 60 tequilas, 58 of them purchased at liquor stores in various Mexican cities, and two directly acquired from a distillery. All the tequilas were of the "white" type, that is, no aged spirits were considered. For the purposes of discrimination and quality control of tequilas, the spectroscopic method that we present here offers an attractive alternative to the traditional methods, like gas chromatography, which is expensive and time-consuming.

  4. Levels of trace elements in different varieties of wheat determined by Atomic Absorption Spectroscopy

    Trace elements Ag, Au, Ca, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, Sr and Zn were determined in six wheat samples purchased from the open market in different localities (Egypt, Saudi Arabia, Yemen, Oman, Dubai and Australia). The dried powdered samples were decomposed in HNO3-HClO4 acids mixtures and elements were determined using recording atomic absorption spectrophotometer. The results were within the safety baseline of all the assayed elements. Certified biological standards, Brown's Kale (BK), Orchard Leaves (OL) and tomato leaves (TOML) were used to assure the accuracy of results. However, Co, Pb and Sr were absent from samples except the Egyptian samples. The obtained databases were statistically treated. Several significant and strong positive correlation coefficients (r=0.506-1.00) between the groups of elements were observed. On the other hand, strong negative correlations (r=0.492-0.873) between another group of elements were also shown. (author)

  5. Far Ultraviolet Spectroscopy of the Intergalactic and Interstellar Absorption Toward 3C 273

    Sembach, Kenneth R.; Howk, J. Christopher; Savage, Blair D.; Shull, J. Michael; Oegerle, William R.; Fisher, Richard R. (Technical Monitor)

    2001-01-01

    We present Far Ultraviolet Spectroscopic Explorer observations of the molecular, neutral atomic, weakly ionized, and highly ionized components of the interstellar and intergalactic material toward the quasar 3C273. We identify Ly-beta absorption in eight of the known intergalactic Ly-alpha absorbers along the sight line with the rest-frame equivalent widths W(sub r)(Ly-alpha) > 50 micro-angstroms. Refined estimates of the H(I) column densities and Doppler parameters (b) of the clouds are presented. We find a range of b = 16-46 km/s. We detect multiple H(I) lines (Ly-beta - Ly-theta) in the 1590 km/s Virgo absorber and estimate logN(H(I)) = 15.85 +/- 0.10, ten times more H(I) than all of the other absorbers along the sight line combined. The Doppler width of this absorber, b = 16 km/s, implies T 4000/Z, where Z is the metallicity. Strong Galactic interstellar O(VI) is present between -100 and +100 km/s with an additional high-velocity wing containing about 13% of the total O(VI) between +100 and +240 km/s. The Galactic O(VI), N(V), and C(IV) lines have similar shapes, with roughly constant ratios across the -100 to +100 km/s velocity range. The high velocity O(VI) wing is not detected in other species. Much of the interstellar high ion absorption probably occurs within a highly fragmented medium within the Loop IV remnant or in the outer cavity walls of the remnant. Multiple hot gas production mechanisms are required. The broad O(VI) absorption wing likely traces the expulsion of hot gas out of the Galactic disk into the halo. A flux limit of 5.4 x 10(epx -16) erg/sq cm/s on the amount of diffuse O(VI) emission present = 3.5' off the 3C273 sight line combined with the observed O(VI) column density toward 3C273, logN O(VI) = 14.73 +/- 0.04, implies n(sub e) < 0.02/cubic cm and P/k < 11,500/cubic cm for an assumed temperature of 3 x 10(exp 5) K. The elemental abundances in the neutral and weakly-ionized interstellar clouds are similar to those found for other halo

  6. Auto-oligomerization and hydration of pyrrole revealed by x-ray absorption spectroscopy

    Near edge x-ray absorption fine structure spectra have been measured at the carbon and nitrogen K-edges of the prototypical aromatic molecule, pyrrole, both in the gas phase and when solvated in water, and compared with spectra simulated using a combination of classical molecular dynamics and first principles density functional theory in the excited state core hole approximation. The excellent agreement enabled detailed assignments. Pyrrole is highly reactive, particularly in water, and reaction products formed by the auto-oligomerization of pyrrole are identified. The solvated spectra have been measured at two different temperatures, indicating that the final states remain largely unaffected by both hydration and temperature. This is somewhat unexpected, since the nitrogen in pyrrole can donate a hydrogen bond to water.

  7. Estimation of lead and zinc in human hair using atomic absorption spectroscopy

    Trace elements analysis in hair can be useful in studying the impact of environmental and dietary factors on human in general for lead and zinc content in hair. Samples of people of different age groups, sex with varied living habits of the individual living in different areas of Sind, urban as well as rural areas were of special interest to be studied to find correlation of socioeconomic factors and the presence of these elements in hair samples. The purpose of this study was to determine whether age, sex and physiological status and environmental pollution affect composition of hair. The method of sample preparation and use of atomic absorption techniques providing unequivocal and direct estimation of metals in ppm/ppb range to arrive upon conclusion. (author)

  8. Reflection-extented-x-ray-absorption-fine-structure spectroscopy at the carbon K-edge

    The authors report an investigation of the carbon K-edge Reflection-Extended X-Ray Absorption Fine Structure (refl-EXAFS) spectra from graphite, diamond and glassy carbon. There is good phase shift transferability between the two well-known bonding types in diamond and graphite, provided that appropriate inner potential corrections to the K-edge energy are made. The model spectra from diamond and graphite were used to investigate the nature of glassy carbon. It was found that, for the particular form of glassy carbon used in this study, the bonding more closely resembled sp3 than sp2. This result is preliminary pending evaluation of the influence of surface oxygen

  9. Auto-oligomerization and hydration of pyrrole revealed by x-ray absorption spectroscopy

    Advanced Light Source; Schwartz, Craig P.; Uejio, Janel S.; Duffin, Andrew M.; England, Alice H.; Prendergast, David; Saykally, Richard J

    2009-05-29

    Near edge x-ray absorption fine structure (NEXAFS) spectra have been measured at the carbon and nitrogen K-edges of the prototypical aromatic molecule, pyrrole, both in the gas phase and when solvated in water, and compared with spectra simulated using a combination of classical molecular dynamics and first principles density functional theory in the excited state core hole approximation. The excellent agreement enabled detailed assignments. Pyrrole is highly reactive, particularly in water, and reaction products formed by the auto-oligomerization of pyrrole are identified. The solvated spectra have been measured at two different temperatures, indicating that the final states remain largely unaffected by both hydration and temperature. This is somewhat unexpected, since the nitrogen in pyrrole can donate a hydrogen bond to water.

  10. Present status of SAGA-LS and x-ray absorption spectroscopy on BL11

    Beamline BL11 at Saga Prefectural Kyushu Synchrotron Light Research Center (SAGA-LS) is a beamline designed to perform X-ray absorption experiments in the 2.1 keV - 23 keV energy range. The sample temperature can be controlled in the range of 15 K - 1073 K using the cryostat and furnaces. Besides the transmission measurement mode using ionization chambers, we can obtain XAFS spectra in fluorescence measurement mode using a Lytle type detector, a silicon drift detector and a 19-element germanium solid-state detector. A conversion electron yield detector is available for layered synthetic materials and bulk sample. In addition, we can also perform in-situ XAFS measurement under toxic and harmful gas atmospheres using quick XAFS measurement system. (author)

  11. A scanned-wavelength-modulation absorption-spectroscopy sensor for temperature and H2O in low-pressure flames

    The design and demonstration of a tunable diode laser sensor for in situ temperature and water (H2O) measurements in laboratory flames is presented. A newly-designed probe consisting of two single-crystal sapphire rods is used to guide 2.9 μm laser light across the core of a flame while avoiding absorption by water outside of the flame. The sensor probes two H2O transitions near 2.9 μm using a scanned-wavelength-modulation absorption-spectroscopy spectral-fitting technique, which enables measurements without calibration or knowledge of the mixture collisional-broadening coefficient. To demonstrate the sensor, temperature and water mole fraction measurements were acquired in stoichiometric, burner-stabilized flames of methane/oxygen/argon at pressures of 25 Torr and 60 Torr. Typical total uncertainties in the temperature and water mole fraction measurements were ±50 K and ±0.016, respectively. This sensor is simple, robust and accurate and enables improved chemical kinetics studies of low-pressure flames. Improvements to reduce temperature and H2O precision to ±20 K and ±0.008, respectively, are discussed. (paper)

  12. Rate-equation model for quantitative concentration measurements in flames with picosecond pump-probe absorption spectroscopy.

    Fiechtner, G J; King, G B; Laurendeau, N M

    1995-02-20

    Measurement of radical concentrations is important in understanding the chemical kinetics involved in combustion. Application of optical techniques allows for the nonintrusive determination of specific radical concentrations. One of the most challenging problems for investigators is to obtain flame data that are independent of the collisional environment. We seek to obviate this difficulty by the use of picosecond pump-probe absorption spectroscopy. A picosecond pump-probe absorption model is developed by rate-equation analysis. Implications are discussed for a laser-pulse width that is much smaller than the excited-state lifetime of the absorbing atom or molecule. The possibility of quantitative, quenching-independent concentration measurements is discussed, and detection limits for atomic sodium and the hydroxyl radical are estimated. For a three-level absorber-emitter, the model leads to a novel pump-probe strategy, called dual-beam asynchronous optical sampling, that can be used to obtain both the electronic quenching-rate coefficient and the doublet mixing-rate coefficient during a single measurement. We discuss the successful demonstration of the technique in a companion paper [Appl. Opt. 34, XXX (1995)]. PMID:21037640

  13. [Research on the influence of LED temperature shifts on differential optical absorption spectroscopy for measuring NO2].

    Ling, Liu-Yi; Xie, Pin-Hua; Qin, Min; Zheng, Ni-Na; Ye, Cong-Lei; Li, Ang; Hu, Ren-Zhi

    2012-11-01

    Influences of LEDs (without etalon structure and center wavelengths are respectively 370 nm (near-UV), 452 nm (blue) and 660 nm(red)) temperature shifts on differential optical absorption spectroscopy(DOAS) for measuring NO2 were studied. NO2 absorption spectra were formed using LED emitting spectra at 10 degrees C. The measured LED spectra at other temperatures were used as reference spectra of DOAS. Thus, NO2 differential optical densities under different LED temperature shifts were acquired and then NO2 differential cross-sections were fitted to the acquired differential optical densities. From fitting results, the linear relations of 0.995, 0.945 and 0.989 correlation between delta of fitting residual and near-UV, blue and red LEDs temperature shifts were found and their slopes are respectively 1.12 x 10(-3), 5.25 x 10(-5) and 7.45 x 10(-4) degrees C(-1). The fitting results show that the influence of temperature shifts of blue LED on DOAS retrieval is negligible and the temperature shifts of near-UV and red LED are impressible to DOAS measurement resulting in degradation of detection sensitivity. The retrieval results of blue LED with and without etalon with similar temperature properties were compared and showed that etalon of LED will greatly increase the influence of temperature shifts of LED on DOAS retrieval. PMID:23387143

  14. Optical feedback cavity-enhanced absorption spectroscopy with a 3.24 μm interband cascade laser

    Manfred, K. M.; Ritchie, G. A. D. [Department of Chemistry, Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Rd, Oxford OX1 3QZ (United Kingdom); Lang, N.; Röpcke, J.; Helden, J. H. van, E-mail: jean-pierre.vanhelden@inp-greifswald.de [Leibniz Institute for Plasma Science and Technology (INP Greifswald), Felix-Hausdorff-Str. 2, 17489 Greifswald (Germany)

    2015-06-01

    The development of interband cascade lasers (ICLs) has made the strong C-H transitions in the 3 μm spectral region increasingly accessible. We present the demonstration of a single mode distributed feedback ICL coupled to a V-shaped optical cavity in an optical feedback cavity-enhanced absorption spectroscopy (OF-CEAS) experiment. We achieved a minimum detectable absorption coefficient, α{sub min}, of (7.1±0.2)×10{sup −8} cm{sup −1} for a spectrum of CH{sub 4} at 3.24 μm with a two second acquisition time (100 scans averaged). This corresponds to a detection limit of 3 ppb CH{sub 4} at atmospheric pressure, which is comparable to previously reported OF-CEAS instruments with diode lasers or quantum cascade lasers. The ability to frequency lock an ICL source in the important 3 μm region to an optical cavity holds great promise for future spectroscopic applications.

  15. Rapid Mapping of Lithiation Dynamics in Transition Metal Oxide Particles with Operando X-ray Absorption Spectroscopy

    Nowack, Lea; Grolimund, Daniel; Samson, Vallerie; Marone, Federica; Wood, Vanessa

    2016-02-01

    Since the commercialization of lithium ion batteries (LIBs), layered transition metal oxides (LiMO2, where M = Co, Mn, Ni, or mixtures thereof) have been materials of choice for LIB cathodes. During cycling, the transition metals change their oxidation states, an effect that can be tracked by detecting energy shifts in the X-ray absorption near edge structure (XANES) spectrum. X-ray absorption spectroscopy (XAS) can therefore be used to visualize and quantify lithiation kinetics in transition metal oxide cathodes; however, in-situ measurements are often constrained by temporal resolution and X-ray dose, necessitating compromises in the electrochemistry cycling conditions used or the materials examined. We report a combined approach to reduce measurement time and X-ray exposure for operando XAS studies of lithium ion batteries. A highly discretized energy resolution coupled with advanced post-processing enables rapid yet reliable identification of the oxidation state. A full-field microscopy setup provides sub-particle resolution over a large area of battery electrode, enabling the oxidation state within many transition metal oxide particles to be tracked simultaneously. Here, we apply this approach to gain insights into the lithiation kinetics of a commercial, mixed-metal oxide cathode material, nickel cobalt aluminium oxide (NCA), during (dis)charge and its degradation during overcharge.

  16. In operando observation system for electrochemical reaction by soft X-ray absorption spectroscopy with potential modulation method

    Nagasaka, Masanari, E-mail: nagasaka@ims.ac.jp; Kosugi, Nobuhiro [Institute for Molecular Science, Myodaiji, Okazaki 444-8585 (Japan); The Graduate University for Advanced Studies, Myodaiji, Okazaki 444-8585 (Japan); Yuzawa, Hayato; Horigome, Toshio [Institute for Molecular Science, Myodaiji, Okazaki 444-8585 (Japan)

    2014-10-15

    In order to investigate local structures of electrolytes in electrochemical reactions under the same scan rate as a typical value 100 mV/s in cyclic voltammetry (CV), we have developed an in operando observation system for electrochemical reactions by soft X-ray absorption spectroscopy (XAS) with a potential modulation method. XAS spectra of electrolytes are measured by using a transmission-type liquid flow cell with built-in electrodes. The electrode potential is swept with a scan rate of 100 mV/s at a fixed photon energy, and soft X-ray absorption coefficients at different potentials are measured at the same time. By repeating the potential modulation at each fixed photon energy, it is possible to measure XAS of electrochemical reaction at the same scan rate as in CV. We have demonstrated successful measurement of the Fe L-edge XAS spectra of aqueous iron sulfate solutions and of the change in valence of Fe ions at different potentials in the Fe redox reaction. The mechanism of these Fe redox processes is discussed by correlating the XAS results with those at different scan rates.

  17. In operando observation system for electrochemical reaction by soft X-ray absorption spectroscopy with potential modulation method

    Nagasaka, Masanari; Yuzawa, Hayato; Horigome, Toshio; Kosugi, Nobuhiro

    2014-10-01

    In order to investigate local structures of electrolytes in electrochemical reactions under the same scan rate as a typical value 100 mV/s in cyclic voltammetry (CV), we have developed an in operando observation system for electrochemical reactions by soft X-ray absorption spectroscopy (XAS) with a potential modulation method. XAS spectra of electrolytes are measured by using a transmission-type liquid flow cell with built-in electrodes. The electrode potential is swept with a scan rate of 100 mV/s at a fixed photon energy, and soft X-ray absorption coefficients at different potentials are measured at the same time. By repeating the potential modulation at each fixed photon energy, it is possible to measure XAS of electrochemical reaction at the same scan rate as in CV. We have demonstrated successful measurement of the Fe L-edge XAS spectra of aqueous iron sulfate solutions and of the change in valence of Fe ions at different potentials in the Fe redox reaction. The mechanism of these Fe redox processes is discussed by correlating the XAS results with those at different scan rates.

  18. In operando observation system for electrochemical reaction by soft X-ray absorption spectroscopy with potential modulation method

    In order to investigate local structures of electrolytes in electrochemical reactions under the same scan rate as a typical value 100 mV/s in cyclic voltammetry (CV), we have developed an in operando observation system for electrochemical reactions by soft X-ray absorption spectroscopy (XAS) with a potential modulation method. XAS spectra of electrolytes are measured by using a transmission-type liquid flow cell with built-in electrodes. The electrode potential is swept with a scan rate of 100 mV/s at a fixed photon energy, and soft X-ray absorption coefficients at different potentials are measured at the same time. By repeating the potential modulation at each fixed photon energy, it is possible to measure XAS of electrochemical reaction at the same scan rate as in CV. We have demonstrated successful measurement of the Fe L-edge XAS spectra of aqueous iron sulfate solutions and of the change in valence of Fe ions at different potentials in the Fe redox reaction. The mechanism of these Fe redox processes is discussed by correlating the XAS results with those at different scan rates

  19. In operando observation system for electrochemical reaction by soft X-ray absorption spectroscopy with potential modulation method.

    Nagasaka, Masanari; Yuzawa, Hayato; Horigome, Toshio; Kosugi, Nobuhiro

    2014-10-01

    In order to investigate local structures of electrolytes in electrochemical reactions under the same scan rate as a typical value 100 mV/s in cyclic voltammetry (CV), we have developed an in operando observation system for electrochemical reactions by soft X-ray absorption spectroscopy (XAS) with a potential modulation method. XAS spectra of electrolytes are measured by using a transmission-type liquid flow cell with built-in electrodes. The electrode potential is swept with a scan rate of 100 mV/s at a fixed photon energy, and soft X-ray absorption coefficients at different potentials are measured at the same time. By repeating the potential modulation at each fixed photon energy, it is possible to measure XAS of electrochemical reaction at the same scan rate as in CV. We have demonstrated successful measurement of the Fe L-edge XAS spectra of aqueous iron sulfate solutions and of the change in valence of Fe ions at different potentials in the Fe redox reaction. The mechanism of these Fe redox processes is discussed by correlating the XAS results with those at different scan rates. PMID:25362423

  20. Rapid Mapping of Lithiation Dynamics in Transition Metal Oxide Particles with Operando X-ray Absorption Spectroscopy.

    Nowack, Lea; Grolimund, Daniel; Samson, Vallerie; Marone, Federica; Wood, Vanessa

    2016-01-01

    Since the commercialization of lithium ion batteries (LIBs), layered transition metal oxides (LiMO2, where M = Co, Mn, Ni, or mixtures thereof) have been materials of choice for LIB cathodes. During cycling, the transition metals change their oxidation states, an effect that can be tracked by detecting energy shifts in the X-ray absorption near edge structure (XANES) spectrum. X-ray absorption spectroscopy (XAS) can therefore be used to visualize and quantify lithiation kinetics in transition metal oxide cathodes; however, in-situ measurements are often constrained by temporal resolution and X-ray dose, necessitating compromises in the electrochemistry cycling conditions used or the materials examined. We report a combined approach to reduce measurement time and X-ray exposure for operando XAS studies of lithium ion batteries. A highly discretized energy resolution coupled with advanced post-processing enables rapid yet reliable identification of the oxidation state. A full-field microscopy setup provides sub-particle resolution over a large area of battery electrode, enabling the oxidation state within many transition metal oxide particles to be tracked simultaneously. Here, we apply this approach to gain insights into the lithiation kinetics of a commercial, mixed-metal oxide cathode material, nickel cobalt aluminium oxide (NCA), during (dis)charge and its degradation during overcharge. PMID:26908198