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Sample records for icp atomic emission

  1. Determination of barium, chromium, cadmium, manganese, lead and zinc in atmospheric particulate matter by inductively coupled plasma atomic emission spectrometry (ICP-AES)

    NASA Astrophysics Data System (ADS)

    Boevski, I. V.; Daskalova, N.; Havezov, I.

    2000-11-01

    The present paper has shown that the Q concept, as proposed by P.W.J.M. Boumans, J.J.A.M. Vrakking, Spectrochim. Acta Part B 43 (1988) 69, can be used as a basic methodology in the determination of Ba, Cr, Cd, Mn, Pb and Zn in pairs of atmospheric particles by inductively coupled plasma atomic emission spectrometry (ICP-AES). The data base of Q values for line interference [ QIj(λ a)] and Q values for wing background interference [ QWJ(Δλ a)] were obtained in our former work [N. Daskalova, Iv. Boevski, Spectral interferences in the determination of trace elements in environmental materials by inductively coupled plasma atomic emission spectrometry, Spectrochim. Acta Part B 54 (1999) 1099-1122]. The samples of atmospheric particles were collected by the Bergerhoff method. The ICP-AES determination was performed after sample digestion with aqua regia. Q values were used for the calculation of both the total interfering signal under the analysis lines and the true detection limits, depending on the matrix constituents in the different samples. Comparative data for the concentration of analytes were obtained by flame atomic absorption spectrometry (FAAS) and direct current arc atomic emission spectrographic method (dc arc-AES).

  2. Spectroscopic characteristics of spiral flow ICP for axially viewing ICP optical emission spectrometry.

    PubMed

    Ohata, Masaki; Kurosawa, Satoru; Shinoduka, Isao; Takaku, Yuichi; Kishi, Yoko

    2015-01-01

    Spectroscopic characteristics of a spiral flow inductively coupled plasma (ICP), which could be sustained stably at 9 L min(-1) of Ar plasma gas flow rate with 1.5 kW RF forward power, were studied for axially viewing ICPOES. The emission intensity profile, excitation temperature and plasma robustness were evaluated, and were similar to those of the standard ICP. The background and emission intensities of elements as well as the excitation behavior for both atom and ion lines were also examined and compared to those of the standard ICP. Since the spectroscopic characteristics of the spiral flow ICP were similar to those of the standard ICP, it could be used as a new low gas flow ICP in axially viewing ICPOES.

  3. The use of inductively coupled plasma-atomic emission spectroscopy (ICP-AES) in the determination of lithium in cleaning validation swabs.

    PubMed

    Lewen, Nancy; Nugent, Dennis

    2010-09-05

    The pharmaceutical industry is required to perform cleaning validation studies to verify that equipment used in the manufacture of pharmaceuticals is adequately cleaned from one product or process to the next. Typically, these cleaning validation studies require an analytical method that uses some form of chromatographic technique. In the case of products that may have an inorganic constituent, however, if can often be easier to verify the cleanliness of equipment by using a non-chromatographic technique. A method is described to certify the cleanliness of processing equipment by determining lithium in cleaning validation swabs using inductively coupled plasma-atomic emission spectroscopy (ICP-AES).

  4. Development and Characterization of a 9-mm Inductively Coupled Argon Plasma (ICP) Source for Atomic Emission Spectrometry.

    DTIC Science & Technology

    1980-09-30

    plus inter- fereni (S.,0:l ol; raio Pal :Ca). Rcati\\,e :;talcs X , 10" V. I0(’ V - ,. ’::ire tO. lffect of P0,, on Ca 11 (393.4 tin) emission profiles...mL- I of Ca while 10 curve B is from tile same solution but with phosphate added at a molar ratio of 50 to 1 (P0 4 : Ca). Profile X was obtained at...emission profiles with changing rf power levels klramne X , 500 W; Y, 750 W). Curve A represcnts amalytc (50 jig mLŕ Ca) signal and curve B awi ]ytc

  5. Separate vaporisation of boric acid and inorganic boron from tungsten sample cuvette-tungsten boat furnace followed by the detection of boron species by inductively coupled plasma mass spectrometry and atomic emission spectrometry (ICP-MS and ICP-AES).

    PubMed

    Kataoka, Hiroko; Okamoto, Yasuaki; Tsukahara, Satoshi; Fujiwara, Terufumi; Ito, Kazuaki

    2008-03-10

    Utilising extremely different vaporisation properties of boron compounds, the determination procedures of volatile boric acid and total boron using tungsten boat furnace (TBF) ICP-MS and TBF-ICP-AES have been investigated. For the determination of volatile boric acid by TBF-ICP-MS, tetramethylammonium hydroxide (TMAH, Me(4)NOH) was used as a chemical modifier to retain it during drying and ashing stages. As for the total boron, not only non-volatile inorganic boron such as boron nitride (BN), boron carbide (B(4)C), etc. but also boric acid (B(OH)(3)) was decomposed by a furnace-fusion digestion with NaOH to produce sodium salt of boron, a suitable species for the electrothermal vaporisation (ETV) procedure. The proposed method was applied to the analysis of various standard reference materials. The analytical results for various biological and steel samples are described.

  6. Determination of heavy metals in bee honey with connected and not connected metal wires using inductively coupled plasma atomic emission spectrometry (ICP-AES).

    PubMed

    Özcan, Mehmet Musa; Al Juhaimi, Fahad Y

    2012-04-01

    Two honey samples are taken from two parts of the same honeycomb: one that contacts to the surface of the wire and the other taken from the surface that does not contact the wires. Heavy metal contents of these two samples were determined by inductively coupled plasma atomic emission spectrometry). The Mo, Cd, Cr, Fe, Mn, Ni and Zn contents of the honey in contact with wire is higher when compared to the other. Especially, Fe and Zn contents of honey in contact with wire is much higher than the non-contact one. These values are, respectively, 190.21 and 112.76 ppm. Besides, Ni content of honey in contact with wire is approximately 50% higher.

  7. Uncertainty Measurement for Trace Element Analysis of Uranium and Plutonium Samples by Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) and Inductively Coupled Plasma-Mass Spectrometry (ICP-MS)

    SciTech Connect

    Gallimore, David L.

    2012-06-13

    The measurement uncertainty estimatino associated with trace element analysis of impurities in U and Pu was evaluated using the Guide to the Expression of Uncertainty Measurement (GUM). I this evalution the uncertainty sources were identified and standard uncertainties for the components were categorized as either Type A or B. The combined standard uncertainty was calculated and a coverage factor k = 2 was applied to obtain the expanded uncertainty, U. The ICP-AES and ICP-MS methods used were deveoped for the multi-element analysis of U and Pu samples. A typical analytical run consists of standards, process blanks, samples, matrix spiked samples, post digestion spiked samples and independent calibration verification standards. The uncertainty estimation was performed on U and Pu samples that have been analyzed previously as part of the U and Pu Sample Exchange Programs. Control chart results and data from the U and Pu metal exchange programs were combined with the GUM into a concentration dependent estimate of the expanded uncertainty. Comparison of trace element uncertainties obtained using this model was compared to those obtained for trace element results as part of the Exchange programs. This process was completed for all trace elements that were determined to be above the detection limit for the U and Pu samples.

  8. [Determination of ru, rh and Pd in 30% trialkyl phosphine oxide (TRPO)-kerosene by inductively coupled plasma-atomic emission spectrum (ICP-AES)].

    PubMed

    Wang, Jian-Chen; Zhang, Lin

    2013-07-01

    The determination method of Ru, Rh and Pd in 30% TRPO-kerosene ICP-AES was studied by using aqueous calibration reference solution and choosing ethanol as diluent. The effects of the contents of 30% TRPO-kerosene and aqueous solution and the concentration of HNO3 in 30% TRPO-kerosene on the intensities of Ru, Rh and Pd were described. The optimized condition for preparing samples and calibration solutions was chosen as follows: The contents of 30% TRPO-kerosene and aqueous phase were 10% (V/V) and 5% (V/V) respectively and the concentration of HNO3 30% TRPO-kerosene was 0.20 mol x L(-1). The determination method of Au, Ru and Pd was set up according to the above condition. The detection limit, precision and recovery ratio of Ru, Rh and Pd are well. The method is not only used in determination of Au, Ru and Pd in 30% TRPO-kerosene, but also used in other organic phases.

  9. Ultraviolet atomic emission detector

    NASA Technical Reports Server (NTRS)

    Braun, W.; Peterson, N. C.; Bass, A. M.; Kurylo, M. J., III (Inventor)

    1972-01-01

    A device and method are provided for performing qualitative and quantitative elemental analysis through the utilization of a vacuum UV chromatographic detector. The method involves the use of a carrier gas at low pressure. The gas carries a sample to a gas chromatograph column; the column output is directed to a microwave cavity. In this cavity, a low pressure microwave discharge produces fragmentation of the compounds present and generates intense atomic emissions in the vacuum ultraviolet. These emissions are isolated by a monochromator and measured by photometer to establish absolute concentration for the elements.

  10. Spontaneous emission by moving atoms

    SciTech Connect

    Meystre, P.; Wilkens, M.

    1994-12-31

    It is well known that spontaneous emission is not an intrinsic atomic property, but rather results from the coupling of the atom to the vacuum modes of the electromagnetic field. As such, it can be modified by tailoring the electromagnetic environment into which the atom can radiate. This was already realized by Purcell, who noted that the spontaneous emission rate can be enhanced if the atom placed inside a cavity is resonant with one of the cavity is resonant with one of the cavity modes, and by Kleppner, who discussed the opposite case of inhibited spontaneous emission. It has also been recognized that spontaneous emission need not be an irreversible process. Indeed, a system consisting of a single atom coupled to a single mode of the electromagnetic field undergoes a periodic exchange of excitation between the atom and the field. This periodic exchange remains dominant as long as the strength of the coupling between the atom and a cavity mode is itself dominant. 23 refs., 6 figs.

  11. Atomic emission spectroscopy

    NASA Technical Reports Server (NTRS)

    Andrew, K. H.

    1975-01-01

    The relationship between the Slater-Condon theory and the conditions within the atom as revealed by experimental data was investigated. The first spectrum of Si, Rb, Cl, Br, I, Ne, Ar, and Xe-136 and the second spectrum of As, Cu, and P were determined. Methods for assessing the phase stability of fringe counting interferometers and the design of an autoranging scanning system for digitizing the output of an infrared spectrometer and recording it on magnetic tape are described.

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

    USGS Publications Warehouse

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

    1985-01-01

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

  13. Tungsten coil atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Rust, Jennifer A.; Nóbrega, Joaquim A.; Calloway, Clifton P.; Jones, Bradley T.

    2006-02-01

    A tungsten coil atomic emission spectrometer is described and evaluated. The system employs a single tungsten coil as a combined atomizer and excitation source for the determination of metals by atomic emission spectrometry. The tungsten coil is extracted from a 150 W, 15 V commercial slide projector light bulb. A simple, laboratory constructed, computer-controlled power supply provides a constant current to the coil. A high-resolution Czerny-Turner monochromator with a charge coupled device detector completes the system. Simultaneous, multi-element analyses are possible within a 4 nm spectral window. Eleven test elements are used to characterize the system: Al (396.1 nm), Co (353.0 nm), Cr (427.1 nm), Dy (404.6 nm), Ga (403.3 nm), K (404.4 nm), Mn (403.1 nm), Pb (405.8 nm), Rb (420.2 nm), Sc (404.8 nm), and Yb (398.7 nm). Tungsten coil atomic emission detection limits are reported for these elements for the first time: 0.02 ng Al, 0.7 ng Co, 0.003 ng Cr, 0.01 ng Dy, 0.7 ng Ga, 0.3 ng K, 0.04 ng Mn, 10 ng Pb, 0.07 ng Rb, 1 ng Sc, and 0.003 ng Yb. The precision for the new technique is better than 13% relative standard deviation for all metals at concentrations two orders of magnitude above the detection limit. Aluminum, Cr, Mn, and K are determined in a standard reference material (trace elements in water) after simple dilution with water, and found values varied from certified values by up to 26%. The average tungsten coil lifetime was found to be 265 heating cycles. The elimination of the external radiation source needed for atomic absorption measurements results in an emission system that could be quite portable.

  14. Determination of trace elements in coal and coal fly ash by joint-use of ICP-AES and atomic absorption spectrometry.

    PubMed

    Iwashita, Akira; Nakajima, Tsunenori; Takanashi, Hirokazu; Ohki, Akira; Fujita, Yoshio; Yamashita, Toru

    2007-01-15

    Microwave-acid digestion (MW-AD) followed by inductively coupled plasma-atomic emission spectrometry (ICP-AES), graphite furnace atomic absorption spectrometry (GFAAS), and hydride generation atomic absorption spectrometry (HGAAS) were examined for the determination of various elements in coal and coal fly ash (CFA). Eight certified reference materials (four coal samples and four CFA samples) were tested. The 10 elements (As, Be, Cd, Co, Cr, Mn, Ni, Pb, Sb, and Se), which are described in the Clean Air Act Amendments (CAAA), were especially considered. For coal, the HF-free MW-AD followed by ICP-AES was successful in the determination of various elements except for As, Be, Cd, Sb, and Se. These elements (except for Sb) were well-determined by use of GFAAS (Be and Cd) and HGAAS (As and Se). For CFA, the addition of HF in the digestion acid mixture was needed for the determination of elements, except for As, Sb, and Se, for which the HF-free MW-AD was applicable. The use of GFAAS (Be and Cd) or HGAAS (Sb and Se) resulted in the successful determination of the elements for which ICP-AES did not work well. The protocol for the determination of the 10 elements in coal and CFA by MW-AD followed by the joint-use of ICP-AES, GFAAS, and HGAAS was established.

  15. Atomic Absorption Spectroscopy, Atomic Emission Spectroscopy, and Inductively Coupled Plasma-Mass Spectrometry

    NASA Astrophysics Data System (ADS)

    Miller, Dennis D.; Rutzke, Michael A.

    Atomic spectroscopy has played a major role in the development of our current database for mineral nutrients and toxicants in foods. When atomic absorption spectrometers became widely available in the 1960s, the development of atomic absorption spectroscopy (AAS) methods for accurately measuring trace amounts of mineral elements in biological samples paved the way for unprecedented advances in fields as diverse as food analysis, nutrition, biochemistry, and toxicology (1). The application of plasmas as excitation sources for atomic emission spectroscopy (AES) led to the commercial availability of instruments for inductively coupled plasma - atomic emission spectroscopy (ICP-AES) beginning in the late 1970s. This instrument has further enhanced our ability to measure the mineral composition of foods and other materials rapidly, accurately, and precisely. More recently, plasmas have been joined with mass spectrometers (MS) to form inductively coupled plasma-mass spectrometer ICP-MS instruments that are capable of measuring mineral elements with extremely low detection limits. These three instrumental methods have largely replaced traditional wet chemistry methods for mineral analysis of foods, although traditional methods for calcium, chloride, iron, and phosphorus remain in use today (see Chap. 12).

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

    SciTech Connect

    Montaser, A.

    1992-01-01

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

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

    SciTech Connect

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

    1999-12-17

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

  18. Testing of Continuous Sampling Air-ICP and Mercury Systems as Continuous Emission Monitors at the Diagnostic Instrumentation and Analysis Laboratory

    SciTech Connect

    D.P. Baldwin; S.J. Bajic; D.E. Eckels; D.S. Zamzow; G.P. Miller; S. Tao; C.A. Waggoner

    2001-03-15

    This report has been prepared to document the performance of the continuous sampling reduced-pressure air-ICP-AES (inductively coupled plasma--atomic emission spectroscopy) and mercury-monitor systems developed by Ames Laboratory for use as continuous emission monitors (CEM). This work was funded by the U. S. Department of Energy, Office of Environmental Management, Office of Science and Technology, through the Mixed Waste Focus Area. The purpose of the project is to develop instrumentation and methods for spectroscopic field monitoring applications. During FY00 this included continued work on the development of the continuous sample introduction system and the multi-frequency AOTF-echelle spectrometer, used in conjunction with the reduced-pressure air-ICP-AES system as a multi-metal CEM. The assembly, development, and testing of an echelle spectrometer system for the detection of mercury (Hg) by atomic absorption was also completed during FY00. The continuous sampling system and the multi-metal air-ICP and mercury-monitor CEM systems were tested at Mississippi State University at the Diagnostic Instrumentation and Analysis Laboratory (DIAL) at the end of FY00. This report describes the characteristics and performance of these systems, and the results of the field tests performed at DIAL.

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

    USGS Publications Warehouse

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

    1987-01-01

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

  20. Solid sampling electrothermal vaporization for sample introduction in inductively coupled plasma atomic emission spectrometry and inductively coupled plasma mass spectrometry

    NASA Astrophysics Data System (ADS)

    Moens, L.; Verrept, P.; Boonen, S.; Vanhaecke, F.; Dams, R.

    1995-06-01

    Solid sampling using electrothermal vaporization is an attractive sample introduction method for atomic absorption spectrometry (AAS), inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS). For AAS, the method is well established. The techniques needed to apply SS-ETV in ICP-based methods are described, with the emphasis on the coupling of different types of ETV-devices to the inductively coupled plasma torch and on the requirements for the spectrometer and the data acquisition and handling system. Though standardization is not straightforward, it is shown that standard addition and external calibration with solid standards yield accurate results. The latter is demonstrated by the analysis of standard reference materials. Figures of merit for SS-ETV-ICP-AES and SS-ETV-ICP-MS are presented. The literature concerning ICP-AES and ICP-MS (methods and applications) is briefly reviewed and new results of SS-ETV-ICP-MS analysis of SRMs are presented.

  1. Coupling dispersive liquid-liquid microextraction to inductively coupled plasma atomic emission spectrometry: An oxymoron?

    PubMed

    Martínez, David; Torregrosa, Daniel; Grindlay, Guillermo; Gras, Luis; Mora, Juan

    2018-01-01

    Coupling dispersive liquid-liquid micro-extraction (DLLME) to inductively coupled plasma atomic emission spectrometry (ICP-AES) is usually troublesome due to the limited plasma tolerance to the organic solvents usually employed for metal extraction. This work explores different coupling strategies allowing the multi-element determination by ICP-AES of the solutions obtained after DLLME procedures. To this end, three of the most common extractant solvents in DLLME procedures (1-undecanol, 1-butyl-3-methyl-imidazolium hexafluorophosphate and chloroform) have been selected to face most of the main problems reported in DLLME-ICP-AES coupling (i.e., those arising from the high solvent viscosity and volatility). Results demonstrate that DLLME can be successfully coupled to ICP-AES after a careful optimization of the experimental conditions. Thus, elemental analysis in 1-undecanol and 1-butyl-3-methyl-imidazolium hexafluorophosphate extracts can be achieved by ICP-AES after a simple dilution step with methanol (1:0.5). Chloroform can be directly introduced into the plasma with minimum changes in the ICP-AES configuration usually employed when operating with aqueous solutions. Diluted inorganic acid solutions (1% w w(-1) either nitric or hydrochloric acids) have been successfully tested for the first time as a carrier for the introduction of organic extractants in ICP-AES. The coupling strategies proposed have been successfully applied to the multi-element analysis (Al, Cu, Fe, Mn, Ni and Zn) of different water samples (i.e. marine, tap and river) by DLLME-ICP-AES. Copyright © 2017 Elsevier B.V. All rights reserved.

  2. Elemental profiling and geographical differentiation of Ethiopian coffee samples through inductively coupled plasma-optical emission spectroscopy (ICP-OES), ICP-mass spectrometry (ICP-MS) and direct mercury analyzer (DMA).

    PubMed

    Habte, Girum; Hwang, In Min; Kim, Jae Sung; Hong, Joon Ho; Hong, Young Sin; Choi, Ji Yeon; Nho, Eun Yeong; Jamila, Nargis; Khan, Naeem; Kim, Kyong Su

    2016-12-01

    This study was aimed to establish the elemental profiling and provenance of coffee samples collected from eleven major coffee producing regions of Ethiopia. A total of 129 samples were analyzed for forty-five elements using inductively coupled plasma (ICP)-optical emission spectroscopy (OES), ICP-mass spectrometry (MS) and direct mercury analyzer (DMA). Among the macro elements, K showed the highest levels whereas Fe was found to have the lowest concentration values. In all the samples, Ca, K, Mg, P and S contents were statistically significant (p<0.05). Micro elements showed the concentrations order of: Mn>Cu>Sr>Zn>Rb>Ni>B. Contents of the trace elements were lower than the permissible standard values. Inter-regions differentiation by cluster analysis (CA), linear discriminant analysis (LDA) and principal component analysis (PCA) showed that micro and trace elements are the best chemical descriptors of the analyzed coffee samples.

  3. Study on Mass Discrimination Effect of Resonance Ionization Mass Spectrometry Using an Inductively Coupled Plasma as an Atomic Source (ICP-RIMS)

    SciTech Connect

    Higuchi, Y.; Watanabe, K.; Tomita, H.; Kawarabayashi, J.; Iguchi, T.

    2009-03-17

    We have proposed a novel concept of Resonance Ionization Mass Spectrometry using an Inductively Coupled Plasma as an Atomic Source (ICP-RIMS). Isotope ratio analysis using ICP-RIMS is expected to be a convenient and precise technique with high throughput. However, the mass discrimination effect caused from difference in kinetic energy of neutral atoms in ICP-RIMS is crucial for precise isotope analysis. We, therefore, investigated the atom kinetic energy distribution introduced into the laser ionization region. The mass-dependent kinetic energy was confirmed in the initial kinetic energy distributions. We preliminary estimated a mass discrimination effect caused by mass-dependent kinetic energy in ICP-RIMS for various detector sizes. We proposed that this effect can be suppressed by selecting the appropriate detector size and adopting the scanning mode of the deflecting voltage.

  4. Determination of additives in PVC material by UV laser ablation inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Hemmerlin, M.; Mermet, J. M.; Bertucci, M.; Zydowicz, P.

    1997-04-01

    UV laser ablation inductively coupled plasma atomic emission spectrometry (LA-ICP-AES) has been applied to the direct determination of additives in solid poly(vinyl chloride) materials. A Nd:YAG laser, operating at its fourth harmonic (266 nm), was used with a beam masking device, in the most reproducible conditions, to introduce solid particles into the plasma torch of a simultaneous ICP-AES system. Emphasis was placed on both precision and accuracy in the analysis of PVC materials by LA-ICP-AES. A series of six in-house PVC reference materials was prepared by incorporating several additives in increasing concentrations. Three alternative methods were evaluated to certify the amount of incorporated elements: ICP-AES with sample dissolution, NAA and XRF. Satisfactory results and good agreement were obtained for seven elements (Al, Ca, Cd, Mg, Sb, Sn and Ti) among the ten incorporated. Sample homogeneity appeared to be satisfactory, and calibration graphs obtained by LA-ICP-AES for several elements are presented. Finally, the performance of the technique in terms of repeatability (1.6-5%), reproducibility (2-5%), and limits of detection was investigated.

  5. Elemental analysis of glass by laser ablation inductively coupled plasma optical emission spectrometry (LA-ICP-OES).

    PubMed

    Schenk, Emily R; Almirall, José R

    2012-04-10

    The elemental analysis of glass evidence has been established as a powerful discrimination tool for forensic analysts. Laser ablation inductively coupled plasma optical emission spectrometry (LA-ICP-OES) has been compared to laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and energy dispersive micro X-ray fluorescence spectroscopy (μXRF/EDS) as competing instrumentation for the elemental analysis of glass. The development of a method for the forensic analysis of glass coupling laser ablation to ICP-OES is presented for the first time. LA-ICP-OES has demonstrated comparable analytical performance to LA-ICP-MS based on the use of the element menu, Al (Al I 396.15 nm), Ba (Ba II 455.40 nm), Ca (Ca II 315.88 nm), Fe (Fe II 238.20 nm), Li (Li I 670.78 nm), Mg (Mg I 285.21 nm), Sr (Sr II 407.77 nm), Ti (Ti II 368.51 nm), and Zr (Zr II 343.82 nm). The relevant figures of merit, such as precision, accuracy and sensitivity, are presented and compared to LA-ICP-MS. A set of 41 glass samples was used to assess the discrimination power of the LA-ICP-OES method in comparison to other elemental analysis techniques. This sample set consisted of several vehicle glass samples that originated from the same source (inside and outside windshield panes) and several glass samples that originated from different vehicles. Different match criteria were used and compared to determine the potential for Type I and Type II errors. It was determined that broader match criteria is more applicable to the forensic comparison of glass analysis because it can reduce the affect that micro-heterogeneity inherent in the glass fragments and a less than ideal sampling strategy can have on the interpretation of the results. Based on the test set reported here, a plus or minus four standard deviation (± 4s) match criterion yielded the lowest possibility of Type I and Type II errors. The developed LA-ICP-OES method has been shown to perform similarly to LA-ICP-MS in the

  6. Comparative determination of Ba, Cu, Fe, Pb and Zn in tea leaves by slurry sampling electrothermal atomic absorption and liquid sampling inductively coupled plasma atomic emission spectrometry.

    PubMed

    Mierzwa, J; Sun, Y C; Chung, Y T; Yang, M H

    1998-12-01

    The comparative determination of barium, copper, iron, lead and zinc in tea leaf samples by two atomic spectrometric techniques is reported. At first, slurry sampling electrothermal atomization atomic absorption spectrometry (ETAAS) was applied. The results of Ba and Pb determination were calculated using the method of standard additions, and results of Cu, Fe and Zn from the calibration graphs based on aqueous standards. These results were compared with the results obtained after microwave-assisted wet (nitric+hydrochloric+hydrofluoric acids) digestion in closed vessels followed by inductively coupled plasma-atomic emission spectrometric (ICP-AES) determination with the calibration by means of aqueous standards. The exception was lead determined after a wet digestion procedure by ETAAS. The accuracy of the studied methods was checked by the use of the certified reference material Tea GBW-07605. The recoveries of the analytes varied in the range from 91 to 99% for slurry sampling ETAAS, and from 92.5 to 102% for liquid sampling ICP-AES. The advantages of slurry sampling ETAAS method are simplicity of sample preparation and very good sensitivity. Slurry sampling ETAAS method is relatively fast but if several elements must be determined in one sample, the time of the whole microwave-assisted digestion procedure and ICP-AES determination will be shorter. However, worse detection limits of ICP-AES must also be taken into the consideration in a case of some analytes.

  7. Conceptual Study on New Isotope Analysis Technique with Resonance Ionization Mass Spectrometry Using Inductively Coupled Plasma as an Atomic Source (ICP-RIMS)

    SciTech Connect

    Watanabe, K.; Uritani, A.; Higuchi, Y.; Tomita, H.; Kawarabayashi, J.; Iguchi, T.

    2009-03-17

    We have proposed the novel isotope analysis technique with Resonance Ionization Mass Spectrometry using Inductively Coupled Plasma as an atomic source (ICP-RIMS). Each component of ICP-RIMS is conceptually designed. We conclude that the orthogonal acceleration time-of-flight mass spectrometer (oa-TOF-MS) driven by a high-repetition-rate pulsed laser would be suitable system for ICP-RIMS. We, additionally, suggest that the first vacuum stage of the vacuum interface, which is between the sampling and skimmer cones, is desired to maintain as low pressure as possible in order to suppress the Doppler broadening and to skim the supersonic jet effectively.

  8. Quantification of 60Fe atoms by MC-ICP-MS for the redetermination of the half-life.

    PubMed

    Kivel, Niko; Schumann, Dorothea; Günther-Leopold, Ines

    2013-03-01

    In many scientific fields, the half-life of radionuclides plays an important role. The accurate knowledge of this parameter has direct impact on, e.g., age determination of archeological artifacts and of the elemental synthesis in the universe. In order to derive the half-life of a long-lived radionuclide, the activity and the absolute number of atoms have to be analyzed. Whereas conventional radiation measurement methods are typically applied for activity determinations, the latter can be determined with high accuracy by mass spectrometric techniques. Over the past years, the half-lives of several radionuclides have been specified by means of multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) complementary to the earlier reported values mainly derived by accelerator mass spectrometry. The present paper discusses all critical aspects (amount of material, radiochemical sample preparation, interference correction, isotope dilution mass spectrometry, calculation of measurement uncertainty) for a precise analysis of the number of atoms by MC-ICP-MS exemplified for the recently published half-life determination of 60Fe (Rugel et al, Phys Rev Lett 103:072502, 2009).

  9. [Determination of trace elements in shark cartilage by inductively coupled plasma atomic emission spectrometry].

    PubMed

    Deng, B; Zhang, Z

    1998-10-01

    Semiquantitative estimation of all elements in shark cartilage was investigated by inductively coupled plasma mass spectrometry (ICP-MS). The determination of trace elements, namely Fe, Zn, Se, Cu, Mn, Mo, Ti and Sr in shark cartilage, was carried out using inductively coupled plasma atomic emission spectrometry (ICP-AES). The matrix effects were overcome by using yttrium as an internal standard element. The recoveries are in the range of 81.6 to 100.7%. The determination limits of Fe, Zn, Se, Cu, Mn, Mo, Ti and Sr are 0.60, 0.55, 0.21, 0.39, 0.042, 0.27, 0.038 and 0.48 microg x g(-1), respectively. The results showed that the shark cartilage contains higher amount of Fe, Zn, Se, Cu, Mn, Mo, Ti and Sr than those in other fishes and in other animal bones.

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

    SciTech Connect

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

    1980-03-01

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

  11. [Determination of total sulfur in coal by inductively coupled plasma atomic emission spectrometry].

    PubMed

    Liu, Dong-yan; Zhang, Yuan-li

    2002-02-01

    A direct method was reported for the determination of total sulfur in coal by inductively coupled plasma atomic emission spectrometry (ICP-AES). The dissolution conditions of coal samples as well as interference conditions of hydrochloric acid and matrix were studied. The recommended method not only proved to be simple and rapid than traditional gravimetric method but show satisfying precision and accuracy as well. The results of samples are as same as gravimetry. The recoveries are more than 96%, and the relative standard deviation of six samples are less than 3%.

  12. Determination of selenium in foods by inductively-coupled plasma atomic emission spectrometry and hydride generation.

    PubMed

    Kardos, J; Zimmer, K; Coni, E; Caroli, S; Stacchini, A

    1989-01-01

    Within the framework of a survey launched by the Istituto Superiore di Sanità to assess the average daily intake of Se with food in the Italian population, a preliminary study was carried out to develop an analytical procedure for the quantification of the element in food products. The method implies the use of a hydride generation system in combination with inductively-coupled plasma atomic emission spectrometry (ICP-AES) and exploits the inherent advantages of this last also for the analysis of non-metals. The overall approach was tested in some Hungarian and Italian foods, adequately lending itself to routine and reliable Se assay.

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

    PubMed

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

    1993-01-01

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

  14. Atomic line emission analyzer for hydrogen isotopes

    DOEpatents

    Kronberg, J.W.

    1991-05-08

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

  15. Atomic line emission analyzer for hydrogen isotopes

    DOEpatents

    Kronberg, J.W.

    1993-03-30

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

  16. Atomic line emission analyzer for hydrogen isotopes

    DOEpatents

    Kronberg, James W.

    1993-01-01

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

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

    SciTech Connect

    Montaser, A.

    1992-09-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-07-01

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

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

    ERIC Educational Resources Information Center

    Horlick, Gary

    1984-01-01

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

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

    ERIC Educational Resources Information Center

    Horlick, Gary

    1984-01-01

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

  1. Depth profiles and bulk analysis of semiconductor materials using ICP mass spectroscopy with electrothermal atomization

    NASA Astrophysics Data System (ADS)

    Faulkner, William; Henderson, William; Rogers, Michael

    1988-10-01

    The purpose of the contract was to build the equipment necessary to show technical feasibility of a Demand Modulated Electrothermal Atomization System. This system was thought to have advantages over current technology as follows: (1) Prevents excessive analyte concentrations in the plasma giving the analyst control over matrix suppression effects. (2) Allows the analyst to control atomization rates and avoid buildup of deposits in the throat of the sample cone opening. (3) Allows the analyst to work in the optimum counting range for isotropic ratio work regardless of concentration variations. (4) Allows the data to be taken over the temperature dimension, thus resolving isobaric interferences as well as improving the signal to noise ratio resulting in improved detection limits across the entire mass range.

  2. [Development of microwave plasma atomic emission detectors for gas chromatography].

    PubMed

    Yuan, Mao; Shi, Yuhua; Yu, Aimin; Zhang, Hanqi; Jin, Qinhan

    2007-05-01

    Three microwave plasmas including microwave induced plasma, capacitively coupled microwave plasma and microwave plasma torch as atomic emission detectors for gas chromatography are evaluated in their history, application and restriction, separately. The development of microwave plasma atomic emission detectors for gas chromatography is prospected.

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

    DOEpatents

    Chan, George C. Y. [Bloomington, IN; Hieftje, Gary M [Bloomington, IN

    2010-08-03

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

  4. [Determination of chlorine in gasoline by inductively coupled plasma atomic emission spectrometry].

    PubMed

    Zhao, Yan; Chen, Xiao-yan; Xu, Dong-yu; Zhang, Shi-yuan; Chen, Ze-yong

    2014-12-01

    A new method was studied for the analysis of chlorine in gasoline by inductively coupled plasma atomic emission spectrometry (ICP-AES). Samples werediluted 1+4(φ) with kerosene. The intense spectral line for chlorine (134.724 nm) was used. In order to eliminate carbon and maintain stable plasma, small amounts of oxygen (0.050 L · min(-1)) were added to the auxiliary gas. The instrumental main condition was optimized in terms of effects of generator power, nebulizer gas flow, auxiliary gas flow, and oxygen flow on SBR for chlorine. Standard addition method was used to compensate matrix effect and signal drift. The recovery for spiking gasoline samples and the limit of detection were in the range of 96.6%~103.9% and 0.27 mg · L(-1) respectively. The relative standard deviation (RSD) was between 1.57% and 4.49%. Compared with microcoulometry, the analysis results of organic chlorine were basically the same. Moreover, chlorine content, including organic chlorine and inorganic chloride was determined by ICP-AES. The proposed method had the advantages of simplicity, speediness and sensitivity, and expanded the ICP-AES application in non-metals especially halogen elements. It can be used for the analysis of chlorine in gasoline and provides technical support for quality evaluation.

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

    NASA Astrophysics Data System (ADS)

    Oropeza, D.

    2016-12-01

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

  6. [Modern spectral estimation of ICP-AES].

    PubMed

    Zhang, Z; Jia, Q; Liu, S; Guo, L; Chen, H; Zeng, X

    2000-06-01

    The inductively coupled plasma atomic emission spectrometry (ICP-AES) and its signal characteristics were discussed using modern spectral estimation technique. The power spectra density (PSD) was calculated using the auto-regression (AR) model of modern spectra estimation. The Levinson-Durbin recursion method was used to estimate the model parameters which were used for the PSD computation. The results obtained with actual ICP-AES spectra and measurements showed that the spectral estimation technique was helpful for the better understanding about spectral composition and signal characteristics.

  7. Photoionization of Endohedral Atoms: Collective, Reflective and Collateral Emissions

    NASA Astrophysics Data System (ADS)

    Chakraborty, Himadri S.; McCune, Matthew A.; Madjet, Mohamed E.; Hopper, Dale E.; Manson, Steven T.

    2009-12-01

    The photoionization properties of a fullerene-confined atom differ dramatically from that of an isolated atom. In the low energy region, where the fullerene plasmons are active, the electrons of the confined atom emerge through a collective channel carrying a significant chunk of plasmon with it. The photoelectron angular distribution of the confined atom however shows far lesser impact of the effect. At higher energies, the interference between two single-electron ionization channels, one directly from the atom and another reflected off the fullerene cage, producuces oscillatory cross sections. But for the outermost atomic level, which transfers some electrons to the cage, oscillations are further modulated by the collateral emission from the part of the atomic charge density transferred to the cage. These various modes of emissions are studied for the photoionization of Ar endohedrally confined in C60.

  8. Photoionization of Endohedral Atoms: Collective, Reflective and Collateral Emissions

    SciTech Connect

    Chakraborty, Himadri S.; McCune, Matthew A.; Hopper, Dale E.; Madjet, Mohamed E.; Manson, Steven T.

    2009-12-03

    The photoionization properties of a fullerene-confined atom differ dramatically from that of an isolated atom. In the low energy region, where the fullerene plasmons are active, the electrons of the confined atom emerge through a collective channel carrying a significant chunk of plasmon with it. The photoelectron angular distribution of the confined atom however shows far lesser impact of the effect. At higher energies, the interference between two single-electron ionization channels, one directly from the atom and another reflected off the fullerene cage, producuces oscillatory cross sections. But for the outermost atomic level, which transfers some electrons to the cage, oscillations are further modulated by the collateral emission from the part of the atomic charge density transferred to the cage. These various modes of emissions are studied for the photoionization of Ar endohedrally confined in C{sub 60}.

  9. Gas-phase ion-molecule reactions for resolution of atomic isobars: AMS and ICP-MS perspectives

    NASA Astrophysics Data System (ADS)

    Bandura, Dmitry R.; Baranov, Vladimir I.; Litherland, A. E.; Tanner, Scott D.

    2006-09-01

    Ion-molecule reactions that can be used for resolution of spectral overlaps of long-lived or stable (T1/2 > 100 years) atomic isobars on the long-lived radio-isotopes (100 < T1/2 < 1012 years) in mass spectrometry are considered. Results for the separations of isobaric overlaps via cation reactions with NO, N2O, O2, CO2, C2H2, CH3F studied with the Inductively Coupled Plasma Dynamic Reaction Cell(TM) Mass Spectrometer (ICP-DRC(TM)-MS) with use of stable isotopes are presented. Overview of potential and reported reactions for separation of 35 isobars is given. Potential for the following isobaric pairs separation is shown (reaction gas and the extent of separation achieved to date in parenthesis): 32Si+/32S+(NO, 5 x 104), 40K+/40Ar+(N2O, 1.9 x 103), 40K+/40Ca+(N2O, 50), 59Ni+/59Co+(N2O, 6), 79Se+/79Br+(O2, 7.2 x 103), 81Kr+/81Br+(C2H2, 1.5 x 104), 93Mo+/93Nb+(N2O, 100), 93Mo+/93Zr+(N2O, 150), 135Cs+/135Ba+(N2O, 8 x 104), 137,138La+/137,138Ba+(O2, 40), 146Sm+/146Nd+(CO2, 1.5 x 105), 176Lu+/176Hf+(NO, 2.8 x 103), 187Re+/187Os+(N2O, 2.8 x 104). Effect of instrumental parameters on reactivity is discussed. The relevance of this work to accelerator mass spectrometry is discussed briefly.

  10. ENVIRONMENTAL APPLICATION OF GAS CHROMATOGRAPHY/ATOMIC EMISSION DETECTION

    EPA Science Inventory

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

  11. ENVIRONMENTAL APPLICATION OF GAS CHROMATOGRAPHY/ATOMIC EMISSION DETECTION

    EPA Science Inventory

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

  12. In situ digestion for the determination of Ca in beverages by tungsten coil atomic emission spectrometry.

    PubMed

    Santos, Luana N; Gonzalez, Mário H; Moura, Monise F; Donati, George L; Nóbrega, Joaquim A

    2012-08-15

    Tungsten coil atomic emission spectrometry (WCAES) is employed for the determination of calcium in juice, mineral and coconut water samples. A sample aliquot of 20 μL is placed directly on the coil and a constant-voltage power source is used to dry and atomize the sample, as well as to promote Ca atomic emission. Analytical signals are resolved and detected using a Czerny-Turner spectrometer and a charge coupled device detector. Some experimental parameters such as coil position related to the spectrometer entrance slit and integration time are critically evaluated. A heating program with relatively constant drying temperatures is used in all measurements. An in situ digestion procedure is used to partially decompose organic matrices and improve WCAES precision and accuracy. By adding an oxidizing mixture to the sample and including a digestion step in the heating cycle, no statistical difference was observed between WCAES and ICP OES results for Ca in juice and coconut water samples. Mineral water samples were simply diluted with 1% vv(-1) HNO(3) before analysis and no significant interference was observed for concomitants such as Na and K. Despite severe positive interference caused by Mg, good agreement was obtained between WCAES and ICP OES results for Ca in several mineral water samples. Limits of detection and quantification obtained were 0.02 and 0.07 mg L(-1), respectively. The method precision, calculated as the relative standard deviation for 10 consecutive measurements of a 2.5 mg L(-1) Ca solution, is 3.8%.

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

    NASA Technical Reports Server (NTRS)

    Schlagen, Kenneth J.

    1992-01-01

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

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

    SciTech Connect

    SEIDEL CM; JAIN J; OWENS JW

    2009-02-23

    This report describes the installation, testing, and acceptance of the Waste Treatment and Immobilization Plant (WTP) procured laser ablation-inductively coupled plasma-atomic emission spectroscopy (LA-ICP-AES) system for remotely analyzing high-level waste (HLW) samples in a hot cell environment. The work was completed by the Analytical Process Development (APD) group in accordance with Task Order 2005-003; ATS MP 1027, Management Plan for Waste Treatment Plant Project Work Performed by Analytical Technical Services. The APD group at the 222-S Laboratory demonstrated acceptable turnaround time (TAT) and provide sufficient data to assess sensitivity, accuracy, and precision of the LA-ICP-AES method.

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

    SciTech Connect

    LOCKREM LL; OWENS JW; SEIDEL CM

    2009-03-26

    This report describes the installation, testing and acceptance of the Waste Treatment and Immobilization Plant procured laser ablation-inductively coupled plasma-atomic emission spectroscopy (LA-ICP-AES) system for remotely analyzing high-level waste samples in a hot cell environment. The 2005-003; ATS MP 1027, Management Plan for Waste Treatment Plant Project Work Performed by Analytical Technical Services. The APD group at the 222-S laboratory demonstrated acceptable turnaround time (TAT) and provide sufficient data to assess sensitivity, accuracy, and precision of the LA-ICP-AES method.

  16. Spreadsheet-Based Program for Simulating Atomic Emission Spectra

    ERIC Educational Resources Information Center

    Flannigan, David J.

    2014-01-01

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

  17. Spreadsheet-Based Program for Simulating Atomic Emission Spectra

    ERIC Educational Resources Information Center

    Flannigan, David J.

    2014-01-01

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

  18. Analysis of tungsten carbide coatings by infrared laser-induced argon spark with inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Kanický, V.; Otruba, V.; Mermet, J.-M.

    2000-10-01

    Infrared laser ablation was studied for application to the analysis of plasma-sprayed tungsten carbide/cobalt coatings. The potential of the laser induced argon-spark (LINA-Spark™), as a sample introduction device in inductively coupled plasma atomic emission spectrometry was studied. The use of an IR laser along with defocusing led to laser-induced microplasma-based ablation. The mass ablation rate, represented by the ICP emission intensity per laser beam unit area, exhibited a flat increase in the irradiance range 2-250 GW/cm 2. A low slope (0.5) of this dependence in log-log scale gave evidence of plasma shielding. The steep increase in the measured acoustic signal when focused in front of the sample, i.e. in argon, indicated a breakdown of argon. Consequently, considerably lower ICP emissions were observed within the same range of irradiance. The cobalt/tungsten line intensity ratio in the ICP was practically constant from 1.5 up to at least 250 GW/cm 2. Acceptable precision (R.S.D.<5%) was obtained without internal standardization for irradiance between 2 and 8 GW/cm 2. Optimization of the laser pulse energy, repetition rate, beam focusing and sample displacement during interaction led to the linearization of dependences of signal vs. cobalt percentage, at least up to the highest studied value of 23% Co.

  19. [Selenium determination in plasma/serum by inductively coupled plasma mass spectrometry (ICP-MS): comparison with graphite furnace atomic absorption spectrometry (GF-AAS)].

    PubMed

    Janasik, Beata; Trzcinka-Ochocka, Małgorzata; Brodzka, Renata

    2011-01-01

    The present study was aimed at comparing two techniques of selenium (Se) determination in serum/plasma samples: inductively coupled plasma mass spectrometry (ICP-MS) and graphite furnace atomic absorption (GF-AAS). Blood samples were collected by venipuncture, using Venosafe closed blood sampling system. The samples were centrifuged. The measurements were performed by Elan DRC-e mass spectrometry, Perkin Elmer, SCIEX, USA and Unicam Solar 989 QZ atomic absorption spectrometry. Reference material, Clincheck Serum Control Level 1 (Recipe, Germany), was used to verify the determinations. The Laboratory participates in external quality control (G-EQUAS). Analytical parameters for both techniques are respectively: ICP-MS--precision 5.9%, limit of detection 0.19 microg/l, repeatability 5.5%, trueness 2.4%, bias 97.6%, GF-AAS--precision 8%, limit of detection 3.4 microg/l, repeatability 7.2%, trueness 6.8%, bias 93.2%. The benefits of the ICP-MS technique are high accuracy, low detection limits and the possibility of multi-element analysis.

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

    NASA Astrophysics Data System (ADS)

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

    1994-07-01

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

  1. Single atom emission in an optical resonator

    SciTech Connect

    Childs, J.J.; An, K.; Dasari, R.R.

    1994-12-31

    A single atom coupled to a single mode of a radiation field is a fundamental system for studying the interaction of radiation with matter. The study of such systems has come to be called cavity quantum electrodynamics (QED). Atoms coupled to a single mode of a resonator have been studied experimentally and theoretically in several interesting regimes since this basic system was first considered theoretically by Janes and Cummings. The objective of the present chapter is to provide a theoretical framework and present a unifying picture of the various phenomena which can occur in such a system. 35 refs., 11 figs.

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

    SciTech Connect

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

    1999-06-10

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

  3. Liquid sample introduction in inductively coupled plasma atomic emission and mass spectrometry - Critical review

    NASA Astrophysics Data System (ADS)

    Bings, N. H.; Orlandini von Niessen, J. O.; Schaper, J. N.

    2014-10-01

    Inductively coupled plasma optical emission spectroscopy (ICP-OES) and mass spectrometry (ICP-MS) can be considered as the most important tools in inorganic analytical chemistry. Huge progress has been made since the first analytical applications of the ICP. More stable RF generators, improved spectrometers and detection systems were designed along with the achievements gained from advanced microelectronics, leading to overall greatly improved analytical performance of such instruments. In contrast, for the vast majority of cases liquid sample introduction is still based on the pneumatic principle as described in the late 19th century. High flow pneumatic nebulizers typically demand the use of spray chambers as “aerosol filters” in order to match the prerequisites of an ICP. By this, only a small fraction of the nebulized sample actually contributes to the measured signal. Hence, the development of micronebulizers was brought forward. Those systems produce fine aerosols at low sample uptake rates, but they are even more prone for blocking or clogging than conventional systems in the case of solutions containing a significant amount of total dissolved solids (TDS). Despite the high number of publications devoted to liquid sample introduction, it is still considered the Achilles' heel of atomic spectrometry and it is well accepted, that the technology used for liquid sample introduction is still far from ideal, even when applying state-of-the-art systems. Therefore, this review is devoted to offer an update on developments in the field liquid sample introduction that had been reported until the year 2013. The most recent and noteworthy contributions to this field are discussed, trends are highlighted and future directions are outlined. The first part of this review provides a brief overview on theoretical considerations regarding conventional pneumatic nebulization, the fundamentals on aerosol generation and discusses characteristics of aerosols ideally suited

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

    PubMed

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

    2016-04-19

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

  5. Determination of silver in nano-plastic food packaging by microwave digestion coupled with inductively coupled plasma atomic emission spectrometry or inductively coupled plasma mass spectrometry.

    PubMed

    Lin, Q-B; Li, B; Song, H; Wu, H-J

    2011-08-01

    The detection of silver in nano-plastic food packaging by microwave digestion coupled with either inductively coupled plasma atomic emission spectrometry (ICP-AES) or inductively coupled plasma mass spectrometry (ICP-MS) was investigated. Microwave digestion was optimised by trialling different acid mixtures. Both ICP-AES and ICP-MS showed good reproducibility, repeatability and recovery. For ICP-AES the limit of detection of the method (LODm) was 25.0 µg g(-1), the limit of detection of the instrument (LODi) was 30.0 ng ml(-1), the linear range was 0.10-10.0 µg ml(-1). The average recoveries for blank samples spiked with silver at 100, 250 and 500 µg g(-1) ranged from 82.53% to 87.60%, and the relative standard deviations (RSDs) were from 1.79% to 8.30%. For ICP-MS analysis the LODm was 0.75 µg g(-1), the LODi was 0.04 ng ml(-1), the linear range was 0.20-500.0 ng ml(-1), the RSDs were 2.26-4.79%, and the recoveries were 78.09-92.72% (spiked concentrations of 2.5, 5.0 and 10.0 µg g(-1)). These results indicate that the proposed method could be employed to analyse silver in nano-plastic food packaging.

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

    PubMed

    Perring, Loïc; Basic-Dvorzak, Marija

    2002-09-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-05-01

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

  8. Analysis of tungsten carbide coatings by UV laser ablation inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Kanicky, V.; Otruba, V.; Mermet, J.-M.

    2000-06-01

    Tungsten carbide coatings (thickness 0.1-0.2 mm) containing 8.0, 12.2, 17.2 and 22.9% Co were studied with laser ablation inductively coupled plasma atomic emission spectrometry (LA-ICP-AES). Composition of these plasma sprayed deposits on steel disks was determined using X-ray fluorescence spectrometry and electron microprobe energy/wavelength dispersive X-ray spectrometry. The coatings were ablated by means of a Q-switched Nd:YAG laser at 266 nm (10 Hz, 10 mJ per shot) coupled to an ICP echelle-based spectrometer equipped with a segmented charge-coupled device detector. Non-linear dependences of cobalt lines intensities on the Co percentage were observed both at a single spot ablation and at a sample translation. This behaviour could be attributed to a complex phase composition of the system W-C-Co. However, employing tungsten as internal standard the linear calibration was obtained for studied analytical lines Co II 228.616 nm, Co II 230.786 nm, Co II 236.379 nm and Co II 238.892 nm.

  9. Simultaneous multielemental analysis of some environmental and biological samples by inductively coupled plasma atomic emission spectrometry

    SciTech Connect

    Hee, S.S.Q.; Boyle, J.R.

    1988-05-15

    The Parr bomb technique is found to be the preferred acid digestion method for multielemental analysis by simultaneous inductively coupled plasma atomic emission spectroscopy (ICP-AES) when compared with microwave and hot plate methods for many environmental and biological specimens, but especially for the latter. One digestion alone often did not produce quantitative results compared with a sequential digestion scheme. The digestions were then refined to be as similar as possible for the various substrates studied. The interference of carbon on As and Se had to be corrected at less than or equal to 3000 ..mu..g of C/mL in the analysis solution, and thus the C content had to be monitored to assess the efficiency of the digestions and to determine if interelemental correction for C presence was required. The C correction was adequate in the range 3000-10,000 ..mu..g of C/ml. The use of modified k values was demonstrated to provide accuracy and had to be used for ICP-AES spectrometers where background corrections were performed first for fixed channels. The results on Cincinnati soils and feces of Cincinnati children showed that Si and Ti were possible tracer elements for soil ingestion by the children.

  10. Inductively coupled plasma-atomic emission spectrometer warning diagnosis procedure using blank solution data

    NASA Astrophysics Data System (ADS)

    Sartoros, Christine; Salin, Eric D.

    1998-05-01

    Lines available while running a blank solution were used to monitor the analytical performance of an inductively coupled plasma atomic emission spectrometry (ICP-AES) system in real time. Using H and Ar lines and their signal-to-background ratios (SBRs), simple rules in the form of a prediction table were developed by inspection of the data. These rules could be used for predicting changes in radio-frequency power, carrier gas flow rates, and sample introduction rate. The performance of the prediction table was good but not excellent. Another set of rules in the form of a decision tree was developed in an automated fashion using the C4.5 induction engine. The performance of the decision tree was superior to that of the prediction table. It appears that blank spectral information can be used to predict with over 90% accuracy when an ICP-AES is breaking down. However this is not as definitive at identifying the exact fault as some more exhaustive approaches involving the use of standard solutions.

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

    PubMed

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

    2007-09-01

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

  12. Atomic emission in the ultraviolet nightglow

    SciTech Connect

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

    1989-12-01

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

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

    SciTech Connect

    Montaser, A.

    1990-01-01

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

  14. High-precision atom localization via controllable spontaneous emission in a cycle-configuration atomic system.

    PubMed

    Ding, Chunling; Li, Jiahua; Yu, Rong; Hao, Xiangying; Wu, Ying

    2012-03-26

    A scheme for realizing two-dimensional (2D) atom localization is proposed based on controllable spontaneous emission in a coherently driven cycle-configuration atomic system. As the spatial-position-dependent atom-field interaction, the frequency of the spontaneously emitted photon carries the information about the position of the atom. Therefore, by detecting the emitted photon one could obtain the position information available, and then we demonstrate high-precision and high-resolution 2D atom localization induced by the quantum interference between the multiple spontaneous decay channels. Moreover, we can achieve 100% probability of finding the atom at an expected position by choosing appropriate system parameters under certain conditions.

  15. A comparative study on electrical characteristics of crystalline AlN thin films deposited by ICP and HCPA-sourced atomic layer deposition

    NASA Astrophysics Data System (ADS)

    Altuntas, Halit; Bayrak, Turkan

    2016-12-01

    In this work, we aimed to investigate the effects of two different plasma sources on the electrical properties of low-temperature plasma-assisted atomic layer deposited (PA-ALD) AlN thin films. To compare the electrical properties, 50 nm thick AlN films were grown on p-type Si substrates at 200 °C by using an inductively coupled RF-plasma (ICP) and a stainless steel hollow cathode plasma-assisted (HCPA) ALD systems. Al/AlN/p-Si metal-insulator-semiconductor (MIS) capacitor devices were fabricated and capacitance versus voltage (C-V) and current-voltage (I-V) measurements performed to assess the basic important electrical parameters such as dielectric constant, effective charge density, flat-band voltage, breakdown field, and threshold voltage. In addition, structural properties of the films were presented and compared. The results show that although HCPA-ALD deposited AlN thin films has structurally better and has a lower effective charge density (N eff ) value than ICP-ALD deposited AlN films, those films have large leakage current, low dielectric constant, and low breakdown field. This situation was attributed to the involvement of Si atoms into the AlN layers during the HCPA-ALD processing leads to additional current path at AlN/Si interface and might impair the electrical properties.

  16. A comparative study on electrical characteristics of crystalline AlN thin films deposited by ICP and HCPA-sourced atomic layer deposition

    NASA Astrophysics Data System (ADS)

    Altuntas, Halit; Bayrak, Turkan

    2017-03-01

    In this work, we aimed to investigate the effects of two different plasma sources on the electrical properties of low-temperature plasma-assisted atomic layer deposited (PA-ALD) AlN thin films. To compare the electrical properties, 50 nm thick AlN films were grown on p-type Si substrates at 200 °C by using an inductively coupled RF-plasma (ICP) and a stainless steel hollow cathode plasma-assisted (HCPA) ALD systems. Al/AlN/ p-Si metal-insulator-semiconductor (MIS) capacitor devices were fabricated and capacitance versus voltage ( C- V) and current-voltage ( I- V) measurements performed to assess the basic important electrical parameters such as dielectric constant, effective charge density, flat-band voltage, breakdown field, and threshold voltage. In addition, structural properties of the films were presented and compared. The results show that although HCPA-ALD deposited AlN thin films has structurally better and has a lower effective charge density ( N eff ) value than ICP-ALD deposited AlN films, those films have large leakage current, low dielectric constant, and low breakdown field. This situation was attributed to the involvement of Si atoms into the AlN layers during the HCPA-ALD processing leads to additional current path at AlN/Si interface and might impair the electrical properties.

  17. Flagging and correcting non-spectral matrix interferences with spatial emission profiles and gradient dilution in inductively coupled plasma-atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Cheung, Yan; Schwartz, Andrew J.; Chan, George C.-Y.; Hieftje, Gary M.

    2015-08-01

    Matrix interference remains one of the most daunting challenges commonly encountered in inductively coupled plasma-atomic emission spectrometry (ICP-AES). In the present study, a method is described that enables identification and correction of matrix interferences in axial-viewed ICP-AES through a combination of spatial mapping and on-line gradient dilution. Cross-sectional emission maps of the plasma are used to indicate the presence of non-spectral (plasma-related and sample-introduction-related) matrix interferences. In particular, apparent concentrations of an analyte species determined at various radial locations in the plasma differ in the presence of a matrix interference, which allows the interference to be flagged. To correct for the interference, progressive, on-line dilution of the sample, performed by a gradient high-performance liquid-chromatograph pump, is utilized. The spatially dependent intensities of analyte emission are monitored at different levels of sample dilution. As the dilution proceeds, the matrix-induced signal variation is reduced. At a dilution where the determined concentrations become independent of location in the plasma, the matrix interference is minimized.

  18. Hydrodemetallation and Hydrodesulfurization Spent Catalysts Elemental Analysis: Comparison of Wavelength Dispersive X-ray Fluorescence and Atomic Emission Spectrometries.

    PubMed

    Garoux, Laetitia; Gourhand, Sébastien; Hébrant, Marc; Schneider, Michel; Diliberto, Sébastien; Meux, Eric

    2017-08-01

    Petroleum industries continuously consume catalysts on very large scales. The recycling of spent catalysts is thus of major economic and environmental importance and its first step consists of the characterization of the valuable metal content. Wavelength dispersive X-ray fluorescence (WDXRF) analysis is compared with inductively coupled plasma atomic emission spectrometry (ICP-AES) for the analysis of five samples of spent hydrodesulphurization (HDS) and hydrodemetallization (HDM) catalysts. The elements are considered for their economic interest (Co, Ni, Mo, and V) or for the problems that can arise when they are present in the sample in significant quantities (Al, As, P, Fe). First, the systematic comparison of the analysis of known synthetic samples was performed. The originality here is that the samples were first beaded with lithium tetraborate (Li2B4O7) for WDXRF analysis and then dissolved in hot HCl 6M for ICP-AES measurements. With this processing, we were able to clearly identify the origin of analytical problems when they arose. Second, the semi-quantitative protocol of WDXRF is compared with the quantitative procedure. Finally, the analysis of the spent catalysts is presented and the information gained by the systematic comparison of ICP-AES and WDXRF is shared. The interest of the simultaneous determination by the two techniques when such complicated heterogeneous matrices are involved is clearly demonstrated.

  19. Laser-induced plasma emission: from atomic to molecular spectra

    NASA Astrophysics Data System (ADS)

    De Giacomo, Alessandro; Hermann, Jörg

    2017-05-01

    The aim of this paper is the description of the optical emission spectral features of the plasma produced by laser-matter interaction, from a fundamental point of view. The laser induced plasma emission spectra are discussed in connection with the basic mechanisms that take place in the plasma phase at different time delays from the laser pulse. The laser induced plasma being a dynamic system, the hierarchy of the elementary mechanisms changes continuously because the electron number density and the electron temperature decrease during the expansion. As a consequence of this, over the duration of the plasma’s persistence the prevailing emitting species changes from ions to atoms and from atoms to molecules. Both atomic and molecular emission spectroscopy are discussed, to convey a complete description of the temporal evolution of laser induced plasma. Current literature, as well as the traditional plasma theories, are presented and discussed in order to give to the reader a general idea of the potentialities and drawbacks of emission spectroscopy in the study of laser induced plasma and its various applications.

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

    NASA Astrophysics Data System (ADS)

    Matusiewicz, Henryk; Barnes, Ramon M.

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

  1. Direct determination of trace elements in niobium, tantalum and their oxides by inductively coupled plasma atomic emission spectrometry after microwave dissolution

    NASA Astrophysics Data System (ADS)

    Grebneva, O. N.; Kubrakova, I. V.; Kudinova, T. F.; Kuz'min, N. M.

    1997-07-01

    Analytical schemes for the determination of trace elements in high-purity niobium, tantalum and their oxides are proposed. The schemes are based on microwave dissolution of the metals and oxides followed by inductively coupled plasma atomic emission spectrometry (ICP-AES) determination of impurities in the solutions. The possibilities of interelement and off-peak background corrections in ICP-AES analysis are discussed. The accuracy of the results obtained is confirmed by the determination of trace elements after a matrix sorption separation procedure. For a number of elements, a comparison of the results obtained by ICP-AES without and with the matrix separation procedure and by electrothermal atomic absorption spectrometry (ETAAS) shows good agreement. The limits of detection for direct ICP-AES determination are in the range 0.4*1.0 μg g -1 for Ba, Ca, Fe, Mg, Mn, Y and La; between 2.0 and 10.0 μ g -1 for B, Cd, Co, Cr, Cu, Hf, Mo, Na, Nb, Ni, Pb, Sr, Ti, Zr and Ta; and for K, Sb and W a detection limit of 20 μ g -1 is achieved. The schemes proposed are intended for rapid routine analysis.

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

    PubMed

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

    2014-06-06

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

  3. Exploration geochemical technique for the determination of preconcentrated organometallic halides by ICP-AES

    USGS Publications Warehouse

    Motooka, J.M.

    1988-01-01

    An atomic absorption extraction technique which is widely used in geochemical exploration for the determination of Ag, As, Au, Bi, Cd, Cu, Mo, Pb, Sb, and Zn has been modified and adapted to a simultaneous inductively coupled plasma-atomic emission instrument. the experimental and operating parameters are described for the preconcentration of the metals into their organometallic halides and for the determination of the metals. Lower limits of determination are equal to or improved over those for flame atomic absorption (except Au) and ICP results are very similar to the accepted AA values, with precision for the ICP data in excess of that necessary for exploration purposes.

  4. Master equation for collective spontaneous emission with quantized atomic motion

    NASA Astrophysics Data System (ADS)

    Damanet, François; Braun, Daniel; Martin, John

    2016-02-01

    We derive a Markovian master equation for the internal dynamics of an ensemble of two-level atoms including all effects related to the quantization of their motion. Our equation provides a unifying picture of the consequences of recoil and indistinguishability of atoms beyond the Lamb-Dicke regime on both their dissipative and conservative dynamics, and applies equally well to distinguishable and indistinguishable atoms. We give general expressions for the decay rates and the dipole-dipole shifts for any motional states, and we find closed-form formulas for a number of relevant states (Gaussian states, Fock states, and thermal states). In particular, we show that dipole-dipole interactions and cooperative photon emission can be modulated through the external state of motion.

  5. Determination of major and trace elements in glycol-based fluids by inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Beckwith, Paul M.

    The development of an analysis based on inductively coupled plasma atomic emission spectrometry (ICP-AES) is reported for the determination of 14 major and trace elements in coolant/antifreeze solutions to provide information on composition of new solutions and wear metals in used solutions. The evaluation of new coolant/antifreeze formulations for aluminum cooling systems has indicated that corrosion protection and stability are strongly dependent on the concentrations of the various components of the solution. The inhibitors include inorganic salts, such as silicates, borates, phosphates and molybdates, and these components are now determined by traditional analytical methods based on gravimetric and titrimetric techniques, spectrophotometry, atomic absorption spectrometry, and ion chromatography. The ICP-AES method may be used to replace these techniques with a simultaneous determination of four inhibitors as well as wear metals in used coolant/antifreeze solutions. The total time for analysis is reduced from several hours to approximately 15 min per sample. The relative standard deviation for the determination of the inhibitors is typically 2%. The detection limit for most of the wear metals is on the order of 0.1 mg l -1.

  6. Negative spontaneous emission by a moving two-level atom

    NASA Astrophysics Data System (ADS)

    Lannebère, Sylvain; Silveirinha, Mário G.

    2017-01-01

    In this paper we investigate how the dynamics of a two-level atom is affected by its interaction with the quantized near field of a plasmonic slab in relative motion. We demonstrate that for small separation distances and a relative velocity greater than a certain threshold, this interaction can lead to a population inversion, such that the probability of the excited state exceeds the probability of the ground state, corresponding to a negative spontaneous emission rate. It is shown that the developed theory is intimately related to a classical problem. The problem of quantum friction is analyzed and the differences with respect to the corresponding classical effect are highlighted.

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

    PubMed

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

    2005-05-13

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

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

    NASA Technical Reports Server (NTRS)

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

    1982-01-01

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

  9. Modelling of Atomic Oxygen Visible emissions from Comets

    NASA Astrophysics Data System (ADS)

    Raghuram, Susarla; Bhardwaj, Anil

    Green (5577 Å) and red-doublet (6300, 6364 Å) lines are prompt emissions of metastable oxygen atoms of O((1) S) and O((1) D) respectively, that have been observed in several comets. The observed red-doublet emission intensity is used to estimate the H_{2}O production rate, whereas the green to red-doublet intensity ratio (G/R ratio) has been used to confirm the parent molecule of oxygen lines as H_{2}O. The observed higher G/R ratio values are ascribed to higher CO_{2} and CO relative abundances. A coupled chemistry-emission model is developed to study the production and loss mechanisms of O((1) S) and O((1) D) atoms and the generation of red and green lines in comets. Our model calculations on different comets suggest that the G/R ratio depends not only on photochemistry, but also on the projected area observed for cometary coma, which is a function of the dimension of the slit used and the geocentric distance of the comet. Our calculated mean excess energy in various photodissociation processes show that the high energy photons dissociate CO_{2} and produce O((1) S) with large velocities than that in photodissociation of H_{2}O which is consistent with larger width of green line compared to that of the red-doublet lines observed in several comets The photodissociation of H_{2}O mainly governs the red-doublet emission, whereas CO_{2} plays an important role in controlling the green line emission. The collisional quenching of O((1) S) and O((1) D) can alter the G/R ratio more than that can be due to variation in the CO_{2} and CO relative abundances. The role of CO photodissociation is found to be insignificant in producing green and red-doublet emission lines and consequently in determining the G/R ratio. If a comet has equal composition of CO_{2} and H_{2}O, which happens when comet is at larger heliocentric distances, then ˜50% of red-doublet emission intensity is controlled by the photodissociation of CO_{2}. References: Festou, M.C., & Feldman, P.D., Astron

  10. On emission from a hydrogen-like atom

    NASA Astrophysics Data System (ADS)

    Skobelev, V. V.

    2016-02-01

    A solution of the Dirac equation for an electron in the field of a point nucleus ( Ze) has been obtained as an eigenfunction of the Schrödinger Hamiltonian and the spin projection operator Σ3. With the use of this solution, the probability W (ν) of the emission of a neutrino per unit time from a hydrogen-like atom, (Ze)* to (Ze) + ν bar ν, has been calculated for the first time in the first order of the parameter Ze ≪ 1. The probability W (ν) appears to be rather small, and the corresponding lifetime τ(ν) = [ W (ν)]-1 is much larger than the age of the Universe; correspondingly, this process cannot affect the balance of low-energy neutrinos. The smallness of W (ν) is due not only to the presence of the obvious "weak" factor ( Gm p 2 )2( m/ mp)4 in the expression for W (ν), but also primarily to the "electromagnetic" factor ( Zα)12, which can be revealed only in a particular calculation. It has been argued within quantum electrodynamics with the mentioned wavefunctions that photon emission, ( Ze)* → ( Ze) + γ, can be absent (analysis of photon emission requires the further development of the method), whereas axion emission, ( Ze)* → ( Ze) + a, can occur, although the last two effects have not been considered in detail.

  11. Electrothermal vaporization — inductively coupled plasma-atomic emission spectrometry for trace metal determination in uranium and thorium compounds without prior matrix separation

    NASA Astrophysics Data System (ADS)

    Purohit, Paru J.; Goyal, Neelam; Thulasidas, S. K.; Page, A. G.; Sastry, M. D.

    2000-08-01

    The electrothermal vaporization (ETV) mode of sample introduction into inductively coupled plasma (ICP) has been examined for its suitability for the analysis of trace metals in uranium and thorium compounds without prior chemical separation of the matrices using atomic emission spectrometry (AES). The ETV interfaced with an ICP torch adapted for glove box operation, has led to determination of sub-nanogram amounts of Al, Be, Ca, Cd, Co, Cr, Cu, Mg, Mn, Na, Ni, Zn, Dy, Eu, Gd and Sm using 10 μl of the sample aliquot containing 200 μg of U/Th matrix with a precision of 1-2%RSD. The results obtained here especially for rare earths in the presence of the matrix are of significance.

  12. Stimulated emission in optically pumped atomic-copper vapor

    SciTech Connect

    Jin Joong Kim; Nackchin Sung

    1987-11-01

    We have observed, for the first time to our knowledge, stimulated emission in atomic-copper vapor that is excited by a resonant tunable laser beam. One of the important and interesting results obtained in this experiment is that excitation of the /sup 2/P/sub 1/2/ level of the copper atoms generates strong amplified spontaneous emission (ASE) for both /sup 2/P/sub 1/2/--/sup 2/D/sub 3/2/ and /sup 2/P/sub 3/2/--/sup 2/D/sub 5/2/ transitions. This is the first reported direct experimental evidence observed for collisional mixing between the /sup 2/P/sub 1/2/ and /sup 2/P/sub 3/2/ levels in a copper-vapor laser. Excitation of the /sup 2/P/sub 3/2/ level induces substantially weaker ASE for the /sup 2/P/sub 1/2/--/sup 2/D/sub 3/2/ transition. In addition, we observed collision-induced ASE for both transitions over a wide range of detuning of the pump frequency. The preliminary results of the experiment are presented, and the implications of the results for high-pressure copper-vapor lasers are discussed.

  13. Modeling Emission of Heavy Energetic Neutral Atoms from the Heliosphere

    NASA Astrophysics Data System (ADS)

    Swaczyna, Paweł; Bzowski, Maciej

    2017-09-01

    Observations of energetic neutral atoms (ENAs) are a fruitful tool for remote diagnosis of the plasma in the heliosphere and its vicinity. So far, instruments detecting ENAs from the heliosphere were configured for observations of hydrogen atoms. Here, we estimate emissions of ENAs of the heavy chemical elements helium, oxygen, nitrogen, and neon. A large portion of the heliospheric ENAs is created in the inner heliosheath from neutralized interstellar pick-up ions (PUIs). We modeled this process and calculated full-sky intensities of ENAs for energies 0.2–130 keV/nuc. We found that the largest fluxes among considered species are expected for helium, smaller for oxygen and nitrogen, and smallest for neon. The obtained intensities are 50–106 times smaller than the hydrogen ENA intensities observed by IBEX. The detection of heavy ENAs will be possible if a future ENA detector is equipped with the capability to measure the masses of observed atoms. Because of different reaction cross-sections among the different species, observations of heavy ENAs can allow for a better understanding of global structure of the heliosphere as well as the transport and energization of PUIs in the heliosphere.

  14. Modelling of the evaporation behaviour of particulate material for slurry nebulization inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Merten, D.; Heitland, P.; Broekaert, J. A. C.

    1997-11-01

    This paper is an electronic publication in Spectrochimica Acta Electronica (SAE), the electronic section of Spectrochimica Acta, Part B (SAB). This hardcopy text, comprising the main body and an appendix, is accompanied by a disk with programs, data files and a brief manual. The main body discusses purpose, design principle and usage of the computer software for modelling the evaporation behaviour of particles in inductively coupled plasma atomic emission spectrometry (ICP-AES). Computer software has been developed in FORTRAN 77 language in order to simulate the evaporation behaviour of particles of refractory materials such as encountered in the analysis of advanced ceramic powders by slurry nebulization inductively coupled argon plasma atomic spectrometry. The program simulates the evaporation of single particles in the inductively coupled plasma and also enable it to calculate on the base of a given particle size distribution the evaporation behaviour of all the particles contained in a sample. In a so-called "intensity concept", the intensity is calculated as a function of the observation height in order to determine recovery rates for slurries compared with aqueous solutions. This yields a quick insight whether a calibration with aqueous solutions can be used for analysis of slurries of a given powder by slurry nebulization ICP-AES and also is a help in determining the optimal parameters for analyses of powders by means of slurry nebulization ICP-AES. Applications for the evaporation of Al 2O 3 and SiC powders document the usefulness of the model for the case of a 1.5 kW argon ICP of which the temperature at 8 mm above the load coil has been determined to be 6100 K. The model predicts the maximum particle size for SiC and Al 2O 3 that can be transported (10-15 μm) and evaporated for a given efficiency under given experimental conditions. For both Al 2O 3 and SiC, two ceramic powders of different grain size were investigated. The median particle sizes cover

  15. Intracavity absorption and emission spectroscopy of atoms in pulsed gas discharges

    SciTech Connect

    Serdyukov, V. I.; Poplavskii, Yu. A.; Sinitsa, L. N.

    2009-07-15

    Absorption and emission spectra of U and Na atoms in the 590-nm spectral range were studied experimentally using pulsed hollow-cathode gas discharges. The spectra were recorded with a high-sensitivity intracavity laser spectrometer. The possibility of generating coherent emission on atomic emission lines in gas-discharge plasmas was demonstrated experimentally.

  16. Determination of metal concentrations in lichen samples by inductively coupled plasma atomic emission spectroscopy technique after applying different digestion procedures.

    PubMed

    Tuncel, S G; Yenisoy-Karakas, S; Dogangün, A

    2004-05-28

    Three digestion procedures have been tested on lichen samples for application in the determination of major, minor and trace elements (Al, Ca, Cd, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, V and Zn) in lichen samples collected in Aegean Region of Turkey by inductively coupled plasma atomic emission spectrometer (ICP-AES). The acid mixture of concentrated HNO(3), H(2)O(2) and HF were used. The instrument was optimized using lichen matrix considering RF power, nebulizer pressure, auxiliary flow rate and pump rate. The accuracy of the overall analyses was first estimated by analysis of two certified reference materials. Good agreement between measured and reference values were found for almost all elements. As the second way of determining the accuracy, results obtained from independent analytical techniques (ICP-AES and instrumental neutron activation analysis (INAA)) were compared for all elements by analyzing real samples. Correlation coefficients of two techniques for the elements ranged between 0.70 (Mg) and 0.96 (Fe). Among the three digestion systems, namely microwave, open vessel and acid bomb, microwave digestion system gave the best recovery results. The method detection limit (MDL) was computed using reagent blanks of microwave digestion system since it provides cleaner sample preparation. Detection limit is adequate for all elements to determine the elements in lichen samples. The precision was assessed from the replicate analyses of reagent blanks of microwave digestion system and was found to be less than 1.5% relative standard deviation (R.S.D.).

  17. Inductively coupled plasma atomic emission spectrometric determination of 27 trace elements in table salts after coprecipitation with indium phosphate.

    PubMed

    Kagaya, Shigehiro; Mizuno, Toshiyuki; Tohda, Koji

    2009-07-15

    The coprecipitation method using indium phosphate as a new coprecipitant has been developed for the separation of trace elements in table salts prior to their determination using inductively coupled plasma atomic emission spectrometry (ICP-AES). Indium phosphate could quantitatively coprecipitate 27 trace elements, namely, Be, Ti, Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, Pb, Sc, Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu, in a table salt solution at pH 10. The rapid coprecipitation technique, in which complete recovery of the precipitate was not required in the precipitate-separation process, was completely applicable, and, therefore, the operation for the coprecipitation was quite simple. The coprecipitated elements could be determined accurately and precisely by ICP-AES using indium as an internal standard element after dissolution of the precipitate with 5 mL of 1 mol L(-1) nitric acid. The detection limits (three times the standard deviation of the blank values, n=10) ranged from 0.001 microg (Lu) to 0.11 microg (Zn) in 300 mL of a 10% (w/v) table salt solution. The method proposed here could be applied to the analyses of commercially available table salts.

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

    ERIC Educational Resources Information Center

    Smith, Gregory D.; And Others

    1995-01-01

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

  19. Metallomics approach to trace element analysis in ustilago maydis using cellular fractionation, atomic absorption spectrometry, and size exclusion chromatography with ICP-MS detection.

    PubMed

    Muñoz, Alma Hortensia Serafin; Kubachka, Kevin; Wrobel, Kazimierz; Corona, Felix Gutierrez; Yathavakilla, Santha K V; Caruso, Joseph A; Wrobel, Katarzyna

    2005-06-29

    Huitlacoche is the ethnic name of the young fruiting bodies of Ustilago maydis, a common parasite of maize. In Mexico and other Latin American countries, this fungus has been traditionally appreciated as a local delicacy. In this work a metallomics approach was used with the determination of eight elements in huitlacoche by electrothermal atomic absorption spectrometry as one facet of this approach. The results obtained indicated relatively lower concentrations of commonly analyzed metals, as referred to the data reported for other mushroom types. This effect was ascribed to different accessibilities of elements, depending on fungus substrate (lower from plant than from soil). Subcellular fractionation was accomplished by centrifugation of cell homogenates suspended in Tris-HCl buffer. Recoveries of the fractionation procedure were in the range of 71-103%. For six elements (Cr, Cu, Fe, Mn, Ni, and Pb), the mean relative contributions in cytosol, cell walls, and mixed membrane fraction were 50.7, 48.2, and 1.1% respectively. To attain the molecular weight distribution of compounds containing target elements as an additional aspect of the metallomics approach, the fungus extract (1% sodium dodecyl sulfate in Tris-HCl, 30 mmol L(-)(1), pH 7.0) was analyzed by size exclusion chromatography with UV and ICP-MS detection. With spectrophotometric detection (280 nm), the elution of high molecular weight compounds was observed in the form of one peak (MW > 10 kDa), and several lower peaks appeared at higher retention times (MW < 10 kDa). On ICP-MS chromatograms, a coelution of (59)Co, (63)Cu, (57)Fe, (202)Hg, (60)Ni, and (80)Se with the first peak on the UV chromatogram was clearly observed, indicating that a fraction of each element incorporated with high molecular weight compounds (12.7, 19.8, 33.7, 100, 19.4, and 45.8%, respectively, based on the peak area measurements). From a comparison of (80)Se and (33)S chromatograms (for sulfur analysis, the extract was obtained in

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

    PubMed

    Wan, Ren-Gang; Zhang, Tong-Yi

    2011-12-05

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

  1. Electron emission in collisions between atoms and dressed projectiles

    NASA Astrophysics Data System (ADS)

    Mondal, A.; Ghosh, T. K.; Mandal, C. R.; Purkait, M.

    2016-12-01

    We present theoretical results for electron emission in collisions between helium atoms and dressed projectiles at high energies. Double-differential cross sections (DDCSs) as a function of the emitted electron energies and angles are calculated. In our study we have applied the three-body formalism using the three-Coulomb wave (3CW-3B) model. The interaction between the dressed projectile and the active electron in the target has been approximated by a model potential having both a long-range Coulomb potential part and a short-range part. However, the active electron in the target has been treated as hydrogenic. We have also studied the projectile charge state dependence of the DDCS. Our theoretical results are compared with available experimental data as well as other theoretical calculations. The comparison shows a good agreement between the present calculations and the measurements. The obtained results are also compatible with other theoretical findings.

  2. Determination of verapamil in pharmaceutical formulations using atomic emission spectrometry.

    PubMed

    Khalil, Sabry; Kelzieh, Ahmed

    2002-01-01

    Ion-associate complexes of verapamil hydrochloride (VpCl) with (Cd(II), Co(II), Mn(II), and Zn(II)) thiocyanates, potassium ferricyanide, and ammonium reineckate are precipitated. The solubility of the solid complexes at the recommended optimum conditions of pH and ionic strength values have been studied. Saturated solutions of each ion associate at different temperatures under the optimum precipitation conditions were prepared and the metal ion contents in the supernatant were determined. The solubility products were thus calculated at different temperatures and the thermodynamic parameters DeltaH, DeltaG, and DeltaS were calculated. A new accurate and precise method based on direct coupled plasma atomic emission spectrometry for the determination of VpCl (1.96-62.86 microg ml(-1)) in pure solutions and pharmaceutical preparations is given.

  3. Determination of Minerals in Apples by ICP AES

    NASA Astrophysics Data System (ADS)

    Duxbury, Mark

    2003-10-01

    A laboratory experiment is described that involves the elemental analysis of apples by inductively coupled plasma atomic emission spectroscopy (IICP AES). The results of the experiment allow students to predict the cold-storage stability of apples. During the experiment the sample-preparation techniques and digestion procedures involved in elemental analysis of solid organic samples are introduced and the optimization of the ICP AES is explored. The method detailed can easily be adapted for the analysis of a wider range of elements. The laboratory experiment may also be undertaken using atomic absorption spectroscopy (AAS) with only minor modifications in the sample-preparation procedure.

  4. High-temperature liquid chromatography inductively coupled plasma atomic emission spectrometry hyphenation for the combined organic and inorganic analysis of foodstuffs.

    PubMed

    Terol, Amanda; Paredes, Eduardo; Maestre, Salvador E; Prats, Soledad; Todolí, José L

    2010-10-01

    The coupling of a High-Temperature Liquid Chromatography system (HTLC) with an Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES) is reported for the first time. This hyphenation combines the separation efficiency of HTLC with the detection power of a simultaneous ICP-AES system and allows the combined determination of organic compound and metals. The effluents of the column were introduced into the spectrometer and the chromatograms for organic compounds were obtained by plotting the carbon emission signal at a characteristic wavelength versus time. As regards metals, they were determined by injecting a small sample volume between the exit of the column and the spectrometer and taking the emission intensity for each one of the elements simultaneously. Provided that in HTLC the effluents emerged at high temperatures, an aerosol was easily generated at the exit of the column. Therefore, the use of a pneumatic nebulizer as a component of a liquid sample introduction system in the ICP-AES could be avoided, thus reducing the peak dispersion and limits of detection by a factor of two. The fact that a hot liquid stream was nebulized made it necessary to use a thermostated spray chamber so as to avoid the plasma cooling as a cause of the excessive mass of solvent delivered to it. Due to the similarity in sample introduction, an Evaporative Light Scattering Detector (ELSD) was taken as a reference. Comparatively speaking, limits of detection were of the same order for both HTLC-ICP-AES and HTLC-ELSD, although the latter provided better results for some compounds (from 10 to 20 mg L(-1) and 5-10 mg L(-1), respectively). In contrast, the dynamic range for the new hyphenation was about two orders of magnitude wider. More importantly, HTLC-ICP-AES provided information about the content of both organic (glucose, sucrose, maltose and lactose at concentrations from roughly 10 to 400 mg L(-1)) as well as inorganic (magnesium, calcium, sodium, zinc, potassium and

  5. Plutonium concentration and (240)Pu/(239)Pu atom ratio in biota collected from Amchitka Island, Alaska: recent measurements using ICP-SFMS.

    PubMed

    Bu, Kaixuan; Cizdziel, James V; Dasher, Douglas

    2013-10-01

    Three underground nuclear tests, including the Unites States' largest, were conducted on Amchitka Island, Alaska. Monitoring of the radiological environment around the island is challenging because of its remote location. In 2008, the Department of Energy (DOE) Office of Legacy Management (LM) became responsible for the long term maintenance and surveillance of the Amchitka site. The first DOE LM environmental survey occurred in 2011 and is part of a cycle of activities that will occur every 5 years. The University of Alaska Fairbanks, a participant in the 2011 study, provided the lichen (Cladonia spp.), freshwater moss (Fontinalis neomexicanus), kelp (Eualaria fistulosa) and horse mussel (Modiolus modiolus) samples from Amchitka Island and Adak Island (a control site). These samples were analyzed for (239)Pu and (240)Pu concentration and (240)Pu/(239)Pu atom ratio using inductively coupled plasma sector field mass spectrometry (ICP-SFMS). Plutonium concentrations and (240)Pu/(239)Pu atom ratios were generally consistent with previous terrestrial and marine studies in the region. The ((239)+)(240)Pu levels (mBq kg(-1), dry weight) ranged from 3.79 to 57.1 for lichen, 167-700 for kelp, 27.9-148 for horse mussel, and 560-573 for moss. Lichen from Adak Island had higher Pu concentrations than Amchitka Island, the difference was likely the result of the higher precipitation at Adak compared to Amchitka. The (240)Pu/(239)Pu atom ratios were significantly higher in marine samples compared to terrestrial and freshwater samples (t-test, p < 0.001); lichen and moss averaged 0.184 ± 0.007, similar to the integrated global fallout ratio, whereas kelp and mussel (soft tissue) averaged 0.226 ± 0.003. These observations provide supporting evidence that a large input of isotopically heavier Pu occurred into the North Pacific Ocean, likely from the Marshall Island high yield nuclear tests, but other potential sources, such as the Kamchatka Peninsula Rybachiy Naval Base and

  6. Atomic Oscillator Strengths by Emission Spectroscopy and Lifetime Measurements

    NASA Astrophysics Data System (ADS)

    Wiese, W. L.; Griesmann, U.; Kling, R.; Musielok, J.

    2002-11-01

    Over the last seven years, we have carried out numerous oscillator strength measurements for some light and medium heavy elements (Musielok et al. 1995, 1996, 1997, 1999, 2000; Veres & Wiese 1996; Griesmann et al. 1997; Bridges & Wiese 1998; Kling et al. 2001; Kling & Gries- mann 2000; Bridges & Wiese to be published). Most recently we have determined numerous transitions of Mu II (Kling et al. 2001; Kling & Griesmann 2000) and are now working on Cl I (Bridges & Wiese to be published). See the summary statement at the end of the text. For the emission measurements, we have applied either a high-current wall-stabilized arc (described for example, in Musielok et al. (1999)), or a high-current hollow cathode, or a Penning discharge. The latter two sources were used for branching ratio measurements from common upper 1ev- els, while the wall-stabilized arc was operated at atmospheric pressure under the condition of partial local thermodynamic equilibrium, which allows the measurement of relative transition probabilities. Absolute data were obtained by combining the emission results with lifetime data measured by other research groups, especially the University of Hannover, with which we have closely collaborated. This group uses the laser induced fluorescence (LIF) technique. Our emission spectra were recorded for the light elements with a 2 m grating spectrometer, or, for Mu II, with an FT 700 vacuum ultraviolet Fourier transform spectrometer. The radiometric calibration was carried out with a tungsten strip lamp for the visible part of the spectrum and with a deuterium lamp for the ultraviolet. All measurements were made under optically thin conditions, which was checked by doubling the path length with a focusing mirror setup. Typical uncertainties of the measured oscillator strengths are estimated to be in the range 15%-20% (one-standard deviation). However, discrepancies with advanced atomic structure theories are sometimes much larger. In Tables 1-3 and Fig. 1, we

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

    NASA Astrophysics Data System (ADS)

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

    2017-04-01

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

  8. Quantification of gadodiamide as Gd in serum, peritoneal dialysate and faeces by inductively coupled plasma atomic emission spectroscopy and comparative analysis by high-performance liquid chromatography.

    PubMed

    Normann PT-; Joffe, P; Martinsen, I; Thomsen, H S

    2000-07-01

    An inductively coupled plasma atomic emission spectroscopy (ICP-AES) method for determination of gadodiamide as Gd in serum, peritoneal dialysate and faeces was developed. The within-day and between-day precision for determination of Gd in serum and peritoneal dialysate were 0.60-2.9 and 1.8-4.4%, respectively, and the accuracy was 98.0-99.3%. The quantification limits in serum and peritoneal dialysate were 6.5 and 1.6 microM Gd, respectively. The within-day and between-day precision determination of gadolinium in faeces were 1.0-5.3 and 2.2-7.9%, respectively, and the accuracy was 104-116%. The quantification limit was 11 nmol Gd/g dry weight. For the high-performance liquid chromatography (HPLC) method, the within-day precision in determination of gadodiamide in peritoneal dialysate was 1.2% and the accuracy was 103%. The quantification limit was 0.9 microM Gd. Comparative analysis of gadodiamide in serum and peritoneal dialysate from severely impaired renal patients by ICP-AES and HPLC revealed no metabolism of chelator or transmetallation of gadolinium, even in samples obtained as long as 7 days after dosing. Furthermore, the ICP-AES determination of Gd in faeces allows for the determination of faeces content of Gd corresponding to less than 0.1% of a clinical dosage of a Gd-based contrast medium.

  9. Portable Dielectric Barrier Discharge-Atomic Emission Spectrometer.

    PubMed

    Li, Na; Wu, Zhongchen; Wang, Yingying; Zhang, Jing; Zhang, Xiangnan; Zhang, Hengnan; Wu, Wenhai; Gao, Jing; Jiang, Jie

    2017-02-21

    This paper describes the first demonstration of a portable dielectric barrier discharge-atomic emission spectrometer (DBD-AES). The instrument primarily consists of a miniature electro-thermal vaporizer (ETV), DBD, and optical signal acquisition units. It weighs only 4.5 kg and is powered by a 24 V DC battery with a maximum power consumption of 37 W. The accompanying software can be operated on a laptop computer. A specially designed quartz tube integrates the ETV unit with the DBD chamber. The effects of experimental parameters were investigated. The limit of detection (LOD) for mercury was 0.4 μg L(-1) (1.2 pg) with a sampling volume of 3 μL. The instrument is applicable for multielement analysis, and the LODs ranged from 0.16 to 11.65 μg L(-1) for Zn, Pb, Ag, Cd, Au, Cu, Mn, Fe, Cr, and As. The instrument was also validated by in-field analysis of seawater samples. The experimental results demonstrated the sensitivity, reliability, and practicality of the instrument.

  10. Use of gradient dilution to flag and overcome matrix interferences in axial-viewing inductively coupled plasma-atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Cheung, Yan; Schwartz, Andrew J.; Hieftje, Gary M.

    2014-10-01

    Despite the undisputed power of inductively coupled plasma-atomic emission spectrometry (ICP-AES), its users still face serious challenges in obtaining accurate analytical results. Matrix interference is perhaps the most important challenge. Dilution of a matrix-containing sample is a common practice to reduce matrix interference. However, determining the optimal dilution factor requires tedious and time-consuming offline sample preparation, since emission lines and the effect of matrix interferences are affected differently by the dilution. The current study exploits this difference by employing a high-performance liquid chromatography gradient pump prior to the nebulizer to perform on-line mixing of a sample solution and diluent. Linear gradient dilution is performed on both the calibration standard and the matrix-containing sample. By ratioing the signals from two emission lines (from the same or different elements) as a function of dilution factor, the analyst can not only identify the presence of a matrix interference, but also determine the optimal dilution factor needed to overcome the interference. A ratio that does not change with dilution signals the absence of a matrix interference, whereas a changing ratio indicates the presence of an interference. The point on the dilution profile where the ratio stabilizes indicates the optimal dilution factor to correct the interference. The current study was performed on axial-viewing ICP-AES with o-xylene as the solvent.

  11. Simultaneous determination of trace heavy metals in ambient aerosols by inductively coupled plasma atomic emission spectrometry after pre-concentration with sodium diethyldithiocarbamate.

    PubMed

    Talebi, S M; Malekiha, M

    2008-07-01

    The simultaneous determination of heavy metals associated with airborne particulate matter in the atmosphere of the city Isfahan (Iran) was performed by inductively coupled plasma atomic emission spectrometry (ICP-AES) after pre-concentration with sodium diethyldithiocarbamate. The preconcentration procedure developed found instrumental to determine the trace heavy metals associated with ambient aerosols collected at a short sampling period or collected from rural areas where the concentrations of these metals are much less than those in urban areas. Several samples were analyzed by both flame atomic absorption spectrometry (FAAS) as a conventional method and the proposed method. The results obtained by the two methods were found in good agreement. The method was applied to the determination of atmospheric level of heavy metals in rural area and also for study of variation in levels of heavy metals in urban atmosphere during the days and nights.

  12. The emission of atoms and molecules accompanying fracture of single-crystal MgO

    NASA Technical Reports Server (NTRS)

    Dickinson, J. T.; Jensen, L. C.; Mckay, M. R.; Freund, F.

    1986-01-01

    The emission of particles due to deformation and fracture of materials has been investigated. The emission of electrons (exoelectron emission), ions, neutral species, photons (triboluminescence), as well as long wavelength electromagnetic radiation was observed; collectively these emissions are referred to as fractoemission. This paper describes measurements of the neutral emission accompanying the fracture of single-crystal MgO. Masses detected are tentatively assigned to the emission of H2, CH4, H2O, CO, O2, CO2, and atomic Mg. Other hydrocarbons are also observed. The time dependencies of some of these emissions relative to fracture are presented for two different loading conditions.

  13. Theoretical study of Na-atom emission from NaCl (100) surfaces

    NASA Astrophysics Data System (ADS)

    Puchin, Vladimir; Shluger, Alexander; Nakai, Yasuo; Itoh, Noriaki

    1994-04-01

    Several models for the elementary processes causing the emission of alkali atoms by electronic excitation of NaCl (100) surfaces have been investigated theoretically. First, the desorption of a Na atom neighboring an electronically excited F center on the surface is simulated using a quantum-mechanical embedded-cluster technique. It is shown that emission of a Na atom is energetically favorable. The kinetics of this process is shown to be controlled by the probability of a nonradiative transition between the two states: the excited state of the F center and that corresponding to a Na atom desorbing from the surface. The potential barrier for desorption of an excited Na atom from the excited F-center state is found to be 2.1 eV. It is also found that the energy for emission of a Na atom from a cluster of F centers (the F3 center) is considerably reduced (for a certain configuration of the defect) with respect to the similar energy for a single F center. The energy barrier for emission of a Na atom neighboring an F' center on the surface is calculated to be 1 eV. It is shown that the electronic excitation of kinklike sites, with a Na atom at the edge, can lead to a barrierless emission of a Na atom, leaving a Vk-type defect behind. The results of calculations are discussed critically on the basis of existing experimental data.

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

    NASA Astrophysics Data System (ADS)

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

    2016-10-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

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

  16. Determination of trace impurities in boron nitride by graphite furnace atomic absorption spectrometry and electrothermal vaporization inductively coupled plasma optical emission spectrometry using solid sampling

    NASA Astrophysics Data System (ADS)

    Barth, P.; Hassler, J.; Kudrik, I.; Krivan, V.

    2007-09-01

    Two digestion-free methods for trace analysis of boron nitride based on graphite furnace atomic absorption spectrometry (GFAAS) and electrothermal vaporization inductively coupled plasma spectrometry optical emission (ETV-ICP-OES) using direct solid sampling have been developed and applied to the determination of Al, Ca, Cr, Cu, Fe, Mg, Mn, Si, Ti and Zr in four boron nitride materials in concentration intervals of 1-23, 54-735, 0.05-21, 0.005-1.3, 1.6-112, 4.5-20, 0.03-1.8, 6-46, 38-170 and 0.4-2.3 μg g - 1 , respectively. At optimized experimental conditions, with both methods, effective in-situ analyte/matrix separation was achieved and calibration could be performed using calibration curves measured with aqueous standard solutions. In solid sampling GFAAS, before sampling, the platform was covered with graphite powder and, for determination of Si, also the Pd/Mg(NO 3) 2 modifier was used. In the determination of all analyte elements by solid sampling ETV-ICP-OES, Freon R12 was added to argon carrier gas. For solid sampling GFAAS and ETV-ICP-OES, the achievable limits of detection were within 5 (Cu)-130 (Si) ng g - 1 and 8 (Cu)-200 (Si) ng g - 1 , respectively. The results obtained by these two methods for four boron nitride materials of different purity grades are compared each with the other and with those obtained in analysis of digests by ICP-OES. The performance of the two solid sampling methods is compared and discussed.

  17. Method development for the determination of manganese, cobalt and copper in green coffee comparing direct solid sampling electrothermal atomic absorption spectrometry and inductively coupled plasma optical emission spectrometry.

    PubMed

    Oleszczuk, Nédio; Castro, Jacira T; da Silva, Márcia M; Korn, Maria das Graças A; Welz, Bernhard; Vale, Maria Goreti R

    2007-10-31

    A method has been developed for the determination of cobalt, copper and manganese in green coffee using direct solid sampling electrothermal atomic absorption spectrometry (SS-ET AAS). The motivation for the study was that only a few elements might be suitable to determine the origin of green coffee so that the multi-element techniques usually applied for this purpose might not be necessary. The three elements have been chosen as test elements as they were found to be significant in previous investigations. A number of botanical certified reference materials (CRM) and pre-analyzed samples of green coffee have been used for method validation, and inductively coupled plasma optical emission spectrometry (ICP OES) after microwave-assisted acid digestion of the samples as reference method. Calibration against aqueous standards could be used for the determination of Mn and Co by SS-ET AAS, but calibration against solid CRM was necessary for the determination of Cu. No significant difference was found between the results obtained with the proposed method and certified or independently determined values. The limits of detection for Mn, Cu and Co were 0.012, 0.006 and 0.004mugg(-1) using SS-ET AAS and 0.015, 0.13 and 0.10mugg(-1) using ICP OES. Seven samples of Brazilian green coffee have been analyzed, and there was no significant difference between the values obtained with SS-ET AAS and ICP OES for Mn and Cu. ICP OES could not be used as a reference method for Co, as essentially all values were below the limit of quantification of this technique.

  18. ICP/MS and ICP/AES elemental analysis (38 elements) of edible wild mushrooms growing in Poland.

    PubMed

    Falandysz, J; Szymczyk, K; Ichihashi, H; Bielawski, L; Gucia, M; Frankowska, A; Yamasaki, S

    2001-06-01

    Thirty-eight elements, including toxic cadmium, lead, mercury, silver and thallium, were determined in 18 species of wild edible mushrooms collected from several sites in Pomorskie Voivodeship in northern Poland in 1994. Elements were determined by double focused high resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) and inductively coupled plasma atomic emission spectroscopy (ICP-AES), after wet digestion of the dried samples with concentrated nitric acid in closed PTFE vessels using a microwave oven. K, P and Mg were present at levels of mg/g dry matter; Na, Zn, Ca, Fe, Cu, Mn, Rb, Ag, Cd, Hg, Pb, Cs, Sr, Al and Si were present at microg/g levels, while Tl, In, Bi, Th, U, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, La, Lu and Ba were present at ng/g levels.

  19. New method for removal of spectral interferences for beryllium assay using inductively coupled plasma atomic emission spectrometry.

    PubMed

    Maxwell, Sherrod L; Bernard, Maureen A; Nelson, Matthew R; Youmans, Linda D

    2008-07-15

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

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

    NASA Astrophysics Data System (ADS)

    Hao, Xiaojian; Liu, Zhenhua; Sang, Tao

    2016-01-01

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

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

    NASA Astrophysics Data System (ADS)

    Ogawa, Shuichi; Tang, Jiayi; Takakuwa, Yuji

    2015-08-01

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

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

    SciTech Connect

    Ogawa, Shuichi Tang, Jiayi; Takakuwa, Yuji

    2015-08-15

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

  3. Emission of fast non-Maxwellian hydrogen atoms in low-density laboratory plasma

    NASA Astrophysics Data System (ADS)

    Brandt, Christian; Marchuk, Oleksandr; Pospieszczyk, Albrecht; Dickheuer, Sven

    2017-03-01

    The source of strong and broad emission of the Balmer-α line in mixed plasmas of hydrogen (or deuterium) and noble gases in front of metallic surfaces is a subject of controversial discussion of many plasma types. In this work the excitation source of the Balmer lines is investigated by means of optical emission spectroscopy in the plasma device PSI-2. Neutral fast non-Maxwellian hydrogen atoms are produced by acceleration of hydrogen ions towards an electrode immersed into the plasma. By variation of the electrode potential the energy of ions and in turn of reflected fast atoms can be varied in the range of 40-300 eV. The fast atoms in front of the electrode are observed simultaneously by an Echelle spectrometer (0.001 nm/channel) and by an imaging spectrometer (0.01 nm/channel) up to few cm in the plasma. Intense excitation channels of the Balmer lines are observed when hydrogen is mixed with argon or with krypton. Especially in Ar-H and Ar-D mixed plasmas the emission of fast hydrogen atoms is very strong. Intermixing hydrogen with other noble gases (He, Ne or Xe) one observes the same effect however the emission is one order of magnitude less compared to Kr-H or Kr-D plasmas. It is shown, that the key process, impacting this emission, is the binary collision between the fast neutral hydrogen atom and the noble gas atom. Two possible sources of excitation are discussed in details: one is the excitation of hydrogen atoms by argon atoms in the ground state and the second one is the process of the so-called excitation transfer between the metastable states of noble gases and hydrogen. In the latter case the atomic data for excitation of Balmer lines are still not available in literature. Further experimental investigations are required to conclude on the source process of fast atom emission.

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

    NASA Technical Reports Server (NTRS)

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

    1973-01-01

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

  5. Visualization of Fermi's golden rule through imaging of light emission from atomic silver chains.

    PubMed

    Chen, Chi; Bobisch, C A; Ho, W

    2009-08-21

    Atomic-scale spatial imaging of one-dimensional chains of silver atoms allows Fermi's golden rule, a fundamental principle governing optical transitions, to be visualized. We used a scanning tunneling microscope (STM) to assemble a silver atom chain on a nickel-aluminum alloy surface. Photon emission was induced with electrons from the tip of the STM. The emission was spatially resolved with subnanometer resolution by changing the tip position along the chain. The number and positions of the emission maxima in the photon images match those of the nodes in the differential conductance images of particle-in-a-box states. This surprising correlation between the emission maxima and nodes in the density of states is a manifestation of Fermi's golden rule in real space for radiative transitions and provides an understanding of the mechanism of STM-induced light emission.

  6. Development of laboratory control samples for the ICP-ES determination of nutrient elements in rat tissues

    NASA Astrophysics Data System (ADS)

    Wolnik, Karen A.; Rader, Jeanne I.; Gaston, Cynthia M.; Fricke, Fred L.

    Laboratory control samples have been prepared from rabbit bones and duodenum and from bovine kidney and spleen for use in quality control and development of methodology for the inductively coupled plasma emission spectroscopy (ICP-ES) determination of 9 elements in weanling rat tissues. Analysis by ICP-ES following wet acid digestion was used to characterize these control samples with respect to mineral content and homogeneity. Results of the investigation of alternative pretreatment techniques are included.

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

    NASA Technical Reports Server (NTRS)

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

    2000-01-01

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

  8. A separation method to overcome the interference of aluminium on zinc determination by inductively coupled plasma atomic emission spectroscopy

    NASA Astrophysics Data System (ADS)

    de Jesus, Djane S.; das Graças Korn, Maria; Ferreira, Sérgio L. C.; Carvalho, Marcelo S.

    2000-04-01

    The use of polyurethane foam (PUF) to separate zinc from large amounts of aluminium and its determination by inductively coupled plasma atomic emission spectroscopy technique (ICP-AES) in aluminium matrices is described. The proposed method is based on the solid-phase extraction of the zinc(II) cation as a thiocyanate complex. Parameters such as effect of pH on zinc sorption, zinc desorption from the foam and analytical features of the procedure were studied. Results showed that the zinc(II) cation within the range from 0.02 to 65.0 μg in 0.2 mol l -1 thiocyanate solution and pH range from 1.0 to 4.0, could be quantitatively extracted by 0.1 g of PUF. The precision of the method was calculated as the relative standard deviation from a series of seven measurements. It was 3.9% for 1.0 μg of zinc in a volume solution of 50 ml. The proposed procedure was used for zinc determination in both aluminium alloys and salts with zinc concentration in the range from 50 to 300 μg g -1. A standard addition technique was used and achieved results showing that this procedure has good accuracy and precision.

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

    SciTech Connect

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

    2008-01-14

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

  10. Determination of hafnium at the 10(-4)% level (relative to zirconium content) using neutron activation analysis, inductively coupled plasma mass spectrometry and inductively coupled plasma atomic emission spectrometry.

    PubMed

    Smolik, Marek; Polkowska-Motrenko, Halina; Hubicki, Zbigniew; Jakóbik-Kolon, Agata; Danko, Bożena

    2014-01-02

    Hafnium at the very low level of 1-8 ppm (in relation to zirconium) was determined in zirconium sulfate solutions (originating from investigations of the separation of ca. 44 ppm Hf from zirconium by means of the ion exchange method) by using three independent methods: inductively coupled plasma mass spectrometry (ICP MS), neutron activation analysis (NAA) and inductively coupled plasma atomic emission spectrometry (ICP-AES). The results of NAA and ICP MS determinations were consistent with each other across the entire investigated range (the RSD of both methods did not exceed 38%). The results of ICP-AES determination were more diverse, particularly at less than 5 ppm Hf (RSD was significantly higher: 29-253%). The ion exchange method exploiting Diphonix(®) resin proved sufficient efficiency in Zr-Hf separation when the initial concentration ratio of the elements ([Zr]0/[Hf]0) ranged from 1200 to ca. 143,000. Copyright © 2013 Elsevier B.V. All rights reserved.

  11. The stability of calibration standards for ICP/AES analysis: Six-month study

    SciTech Connect

    Huff, E.A.; Huff, D.R.

    1992-05-01

    The stability of instrument calibration standards for Inductively Coupled Plasma/Atomic Emission Spectrometric (ICP/AES) analysis was studied over a six-month period. Data were obtained as functions of analyte concentration, acid type, and acidity. The impact of acid concentration on signal-to-background ratios (S/B) was also assessed. The results show that analytes maintain their integrity over extended periods with appropriate inorganic acid preservatives. Thus, frequent standard preparations become unnecessary to obtain valid analytical data.

  12. Integrated Design for Marketing and Manufacturing team: An examination of LA-ICP-AES in a mobile configuration. Final report

    SciTech Connect

    Not Available

    1994-05-01

    The Department of Energy (DOE) has identified the need for field-deployable elemental analysis devices that are safer, faster, and less expensive than the fixed laboratory procedures now used to screen hazardous waste sites. As a response to this need, the Technology Integration Program (TIP) created a mobile, field-deployable laser ablation-inductively coupled plasma-atomic emission spectrometry (LA-ICP-AES) sampling and analysis prototype. Although the elemental. screening prototype has been successfully field-tested, continued marketing and technical development efforts are required to transfer LA-ICP-AES technology to the commercial sector. TIP established and supported a student research and design group called the Integrated Design for Marketing and Manufacturing (IDMM) team to advance the technology transfer of mobile, field-deployable LA-ICP-AES. The IDMM team developed a conceptual design (which is detailed in this report) for a mobile, field-deployable LA-ICP-AES sampling and analysis system, and reports the following findings: Mobile, field-deployable LA-ICP-AES is commercially viable. Eventual regulatory acceptance of field-deployable LA-ICP-AES, while not a simple process, is likely. Further refinement of certain processes and components of LA-ICP-AES will enhance the device`s sensitivity and accuracy.

  13. Steelmaking process control using remote ultraviolet atomic emission spectroscopy

    NASA Astrophysics Data System (ADS)

    Arnold, Samuel

    Steelmaking in North America is a multi-billion dollar industry that has faced tremendous economic and environmental pressure over the past few decades. Fierce competition has driven steel manufacturers to improve process efficiency through the development of real-time sensors to reduce operating costs. In particular, much attention has been focused on end point detection through furnace off gas analysis. Typically, off-gas analysis is done with extractive sampling and gas analyzers such as Non-dispersive Infrared Sensors (NDIR). Passive emission spectroscopy offers a more attractive approach to end point detection as the equipment can be setup remotely. Using high resolution UV spectroscopy and applying sophisticated emission line detection software, a correlation was observed between metal emissions and the process end point during field trials. This correlation indicates a relationship between the metal emissions and the status of a steelmaking melt which can be used to improve overall process efficiency.

  14. Preparation of three-dimensional entanglement for distant atoms in coupled cavities via atomic spontaneous emission and cavity decay

    PubMed Central

    Su, Shi-Lei; Shao, Xiao-Qiang; Wang, Hong-Fu; Zhang, Shou

    2014-01-01

    We propose a dissipative scheme to prepare a three-dimensional entangled state for two atoms trapped in separate coupled cavities. Our work shows that both atomic spontaneous emission and cavity decay, which are two typical obstacles in unitary-dynamics-based schemes, are no longer detrimental, but necessary for three-dimensional entangled state preparation without specifying initial state and controlling the evolution time precisely. Final numerical simulation with one group of experimental parameters indicates that the performance of our scheme could be better than the unitary-dynamics-based scheme. PMID:25523944

  15. Forbidden line emission from highly ionized atoms in tokamak plasmas

    NASA Technical Reports Server (NTRS)

    Feldman, U.; Doschek, G. A.; Bhatia, A. K.

    1982-01-01

    Considerable interest in the observation of forbidden spectral lines from highly ionized atoms in tokamak plasmas is related to the significance of such observations for plasma diagnostic applications. Atomic data for the elements Ti Cr, Mn, Fe, Ni, and Kr have been published by Feldman et al. (1980) and Bhatia et al. (1980). The present investigation is concerned with collisional excitation rate coefficients and radiative decay rates, which are interpolated for ions of elements between calcium, and krypton and for levels of the 2s2 2pk, 2s 2p(k+1), and 2p(k+2) configurations, and for the O I, N I, C I, B I, and Be I isoelectronic sequences. The provided interpolated atomic data can be employed to calculate level populations and relative line intensities for ions of the considered sequences, taking into account levels of the stated configurations. Important plasma diagnostic information provided by the forbidden lines includes the ion temperature

  16. Ultraviolet Absorption Spectrometry (UVAS) and Liquid Atomic Emission Spectrometry (LAES.

    DTIC Science & Technology

    1994-02-10

    salinity information. The system worked fairly well, although the flow rate was less than optimum. However, after a deep freeze in early January, the...significantly smaller heat sink. The absorbance flow cell system was modified to include two flow cells. Having two flow cells allows the operator to...excitation spectra. After the emission power supply, the emission flow cell is the second most critical component of the LAES system . A diagram of the

  17. Inductively coupled plasma atomic emission spectroscopic determination of rare earth elements in geological samples after preconcentration by countercurrent chromatography—I

    NASA Astrophysics Data System (ADS)

    Pukhovskaya, V. M.; Maryutina, T. A.; Grebneva, O. N.; Kuz'min, N. M.; Spivakov, B. Ya.

    1993-09-01

    Countercurrent chromatography (CCC) was applied to group pre-separation of rare earth elements (REE) in rocks. A 0.5 mol/l solution of di-2-ethylhexylphosphoric acid (D2EHPA) in n-decane as stationary phase, and aqueous HC1 solution as mobile phase were used. Experimental conditions were found for quantitative separation of REE from the rock constituents that interfere with their inductively coupled plasma atomic emission spectrometry (ICP-AES) determination. The complete preseparation procedure takes 40 min at a mobile phase pumping rate of 2 ml/min. Interelement and off-peak background corrections were applied to compensate for the contributions of mutual spectral interferences to the analyte line and background intensities. Standard reference rock materials and samples of different composition with well known REE contents were analysed. The data obtained are in good agreement with certified and previously determined values, except for "heavy" REE such as Tm, Yb and Lu.

  18. Determination of iron, cobalt, nickel, manganese, zinc, copper, cadmium and lead in human hair by inductively coupled plasma-atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Sreenivasa Rao, K.; Balaji, T.; Prasada Rao, T.; Babu, Y.; Naidu, G. R. K.

    2002-08-01

    A method was standardized for the dissolution of hair samples and analysis was carried out by inductively coupled plasma atomic emission spectrometry (ICP-AES). Hair samples were brought into solution by using a mixture of nitric acid and hydrogen peroxide. Various parameters that influence the sample preparation, namely temperature, digestion time and ratio of acid mixture were studied and standardized. The optimized method has been employed to digest standard reference materials and hair samples of residents of India, collected from different age groups and sex, and analyzed for Fe, Co, Ni, Mn, Zn, Cu, Cd and Pb. The values agree for most of the metals with the data reported for human hair samples of residents of India. The NIES CRM Human Hair No. 5 and IAEA Reference Hair HH-1 certified reference materials were used in order to verify the accuracy of the method and the results were in excellent agreement with the certified values.

  19. Calibration graphs for Ti, Ta and Nb in sintered tungsten carbide by infrared laser ablation inductively coupled plasma atomic emission spectrometry.

    PubMed

    Kanický, V; Otruba, V; Mermet, J M

    2001-12-01

    Infrared laser ablation (IR-LA) has been studied as a sample introduction technique for the analysis of sintered cobalt-cemented tungsten carbide materials by inductively coupled plasma atomic emission spectrometry (ICP-AES). Fractionation of cobalt was observed. Linearity of calibration plots was verified at least up to 15% Ti, 8% Ta, and 3% Nb. Above 1% (m/m) Ti, Ta, and Nb, the repeatability of results was better than 3% R.S.D. The relative uncertainty at the centroid of the calibration line was in the range from +/- 3% to +/- 4% for Ti, Ta, and Nb with internal standardization by tungsten and up to +/- 5% without internal standardization. The limits of detection were 0.004% Ti, 0.001% Ta, and 0.004% Nb. Elimination of the cemented hardmetal dissolution procedure is the main advantage of this method.

  20. Applications of high resolution ICP-AES in the nuclear industry

    SciTech Connect

    Johnson, S.G.; Giglio, J.J.; Goodall, P.S.; Cummings, D.G.

    1998-07-01

    Application of high resolution ICP-AES to selected problems of importance in the nuclear industry is a growing field. The advantages in sample preparation time, waste minimization and equipment cost are considerable. Two examples of these advantages are presented in this paper, burnup analysis of spent fuel and analysis of major uranium isotopes. The determination of burnup, an indicator of fuel cycle efficiency, has been accomplished by the determination of {sup 139}La by high resolution inductively coupled plasma atomic emission spectroscopy (HR-ICP-AES). Solutions of digested samples of reactor fuel rods were introduced into a shielded glovebox housing an inductively coupled plasma (ICP) and the resulting atomic emission transmitted to a high resolution spectrometer by a 31 meter fiber optic bundle. Total and isotopic U determination by thermal ionization mass spectrometry (TIMS) is presented to allow for the calculation of burnup for the samples. This method of burnup determination reduces the time, material, sample handling and waste generated associated with typical burnup determinations which require separation of lanthanum from the other fission products with high specific activities. Work concerning an alternative burnup indicator, {sup 236}U, is also presented for comparison. The determination of {sup 235}U:{sup 238}U isotope ratios in U-Zr fuel alloys is also presented to demonstrate the versatility of HR-ICP-AES.

  1. ICP Source with Immersed Ferromagnetic Inductor

    NASA Astrophysics Data System (ADS)

    Godyak, Valery

    2013-09-01

    Inductively coupled plasma (ICP) sources have found a wide range of applications in various areas of plasma science and technology. Among different ICP topology, ICPs with immersed inductors have benefits (compared to ICPs with helical side or flat top inductors) of better coupling and electromagnetic (EM) field self-screening by the plasma surrounding the inductor. This allows for EM-free otter plasma boundary, thus making an ICP chamber entirely of metal or glass, with no EM radiation outside the plasma. It's been long known that ICP enhanced with ferromagnetic core immersed inductor is applicable in rf light sources and has demonstrated good performance. In this presentation we report a detailed experimental study of the electrical and plasma characteristics of compact ICPs with immersed ferromagnetic inductors in argon and xenon gas. The extremely high plasma transfer efficiency of this plasma source has been demonstrated in a wide range of gas pressure and rf power. A compact plasma cathode built with ICP having an immersed ferromagnetic inductor, and operating at 70-200 W has shown high power transfer efficiency of 97%, and electron emission efficiency of 25 mA/W. These data are superior compared to those demonstrated for other plasma cathodes.

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

    NASA Astrophysics Data System (ADS)

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

    2007-11-01

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

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

    PubMed

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

    2014-01-07

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

  4. Time evolution, Lamb shift, and emission spectra of spontaneous emission of two identical atoms

    SciTech Connect

    Wang Dawei; Li Zhenghong; Zheng Hang; Zhu Shiyao

    2010-04-15

    A unitary transformation method is used to investigate the dynamic evolution of two multilevel atoms, in the basis of symmetric and antisymmetric states, with one atom being initially prepared in the first excited state and the other in the ground state. The unitary transformation guarantees that our calculations are based on the ground state of the atom-field system and the self-energy is subtracted at the beginning. The total Lamb shifts of the symmetric and antisymmetric states are divided into transformed shift and dynamic shift. The transformed shift is due to emitting and reabsorbing of virtual photons, by a single atom (nondynamic single atomic shift) and between the two atoms (quasi-static shift). The dynamic shift is due to the emitting and reabsorbing of real photons, by a single atom (dynamic single atomic shift) and between the two atoms (dynamic interatomic shift). The emitting and reabsorbing of virtual and real photons between the two atoms result in the interatomic shift, which does not exist for the one-atom case. The spectra at the long-time limit are calculated. If the distance between the two atoms is shorter than or comparable to the wavelength, the strong coupling between the two atoms splits the spectrum into two peaks, one from the symmetric state and the other from the antisymmetric state. The origin of the red or blue shifts for the symmetric and antisymmetric states mainly lies in the negative or positive interaction energy between the two atoms. In the investigation of the short time evolution, we find the modification of the effective density of states by the interaction between two atoms can modulate the quantum Zeno and quantum anti-Zeno effects in the decays of the symmetric and antisymmetric states.

  5. Sustainability of Rotrode Atomic Emission Spectrometry for Wear Deris

    DTIC Science & Technology

    2006-10-04

    Most customers will have increasing expectations as a result of normal consumerism and readily apparent technological progress. 1.2. Rotrode atomic...experience. It can be run on a ship or a tarmac. Although environmental conditions and operator proficiency, among other factors, can affect the quality of...oil, LIBS is gaining headway in environmental , structural, pathological, and pharmaceutical testing. Lasers will continue to get smaller, cheaper, more

  6. Size-based analysis of incinerator fly ash using gravitational SPLITT fractionation, sedimentation field-flow fractionation, and inductively coupled plasma-atomic emission spectroscopy.

    PubMed

    Kim, Won-Suk; Park, Mira; Lee, Dai Woon; Moon, Myeong Hee; Lim, Heungbin; Lee, Seungho

    2004-02-01

    Fly ash has been regarded as hazardous because of its high adsorption of toxic organic and/or inorganic pollutants. Fly ash is also known to have broad distributions of different chemical and physical properties, such as size and density. In this study, fly ash emitted from a solid waste incinerator was pre-fractionated into six sub-populations by use of gravitational SPLITT fractionation (GSF). The GSF fractions were then analyzed by sedimentation field-flow fractionation (SdFFF) and ICP-AES. SdFFF analysis showed the fly ash has a broad size distribution ranging from a few nanometers up to about 50 microm. SdFFF results were confirmed by electron microscopy. Inductively coupled plasma-atomic emission spectroscopy (ICP-AES) analysis of the GSF fractions showed the fly-ash particles contain a variety of inorganic elements including Ca, Si, Mg, Fe, and Pb. The most abundant in fly ash was Ca, followed by Si then Mg. No correlations were found between trace element concentration and particle size.

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

    SciTech Connect

    LaFreniere, K.E.

    1986-06-01

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

  8. Multi-element analysis using inductively coupled plasma mass spectrometry and inductively coupled plasma atomic emission spectroscopy for provenancing of animals at the continental scale.

    PubMed

    Kreitals, Natasha M; Watling, R John

    2014-11-01

    Chemical signatures within the environment vary between regions as a result of climatological, geochemical and anthropogenic influences. These variations are incorporated into the region's geology, soils, water and vegetation; ultimately making their way through the food chain to higher level organisms. Because the variation in chemical signatures between areas is significant, a specific knowledge of differences in elemental distribution patterns between, and within populations, could prove beneficial for provenancing animals or animal related products when applied to indigenous and feral faunal populations. The domestic pig (Sus scrofa domestica) was used as an investigative model to determine the feasibility of using a chemical traceability method for the provenance determination of animal tissue. Samples of pig muscle, tongue, stomach, heart, liver and kidney were collected from known farming areas around Australia. Samples were digested in 1:3 H2O2:HNO3 and their elemental composition determined using solution based Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS). Pigs from different growing regions in Australia could be distinguished based on the chemical signature of each individual tissue type. Discrimination was possible at a region, state and population level. This investigation demonstrates the potential for multi-element analysis of low genetic variation native and feral species of forensic relevance.

  9. Comparative measurements of mineral elements in milk powders with laser-induced breakdown spectroscopy and inductively coupled plasma atomic emission spectroscopy.

    PubMed

    Lei, W Q; El Haddad, J; Motto-Ros, V; Gilon-Delepine, N; Stankova, A; Ma, Q L; Bai, X S; Zheng, L J; Zeng, H P; Yu, J

    2011-07-01

    Mineral elements contained in commercially available milk powders, including seven infant formulae and one adult milk, were analyzed with inductively coupled plasma atomic emission spectrometry (ICP-AES) and laser-induced breakdown spectroscopy (LIBS). The purpose of this work was, through a direct comparison of the analytical results, to provide an assessment of the performance of LIBS, and especially of the procedure of calibration-free LIBS (CF-LIBS), to deal with organic compounds such as milk powders. In our experiments, the matrix effect was clearly observed affecting the analytical results each time laser ablation was employed for sampling. Such effect was in addition directly observed by determining the physical parameters of the plasmas induced on the different samples. The CF-LIBS procedure was implemented to deduce the concentrations of Mg and K with Ca as the internal reference element. Quantitative analytical results with CF-LIBS were validated with ICP-AES measurements and nominal concentrations specified for commercial milks. The obtained good results with the CF-LIBS procedure demonstrate its capacity to take into account the difference in physical parameters of the plasma in the calculation of the concentrations of mineral elements, which allows a significant reduction of the matrix effect related to laser ablation. We finally discuss the way to optimize the implementation of the CF-LIBS procedure for the analysis of mineral elements in organic materials.

  10. Determination of rare earth elements in geological samples by inductively coupled plasma atomic emission spectrometry with flow injection liquid-liquid extraction.

    PubMed

    Xu, Zhifang; Liu, Congqiang; Zhang, Hongxiang; Ma, Yingjun; Lin, Soulin

    2003-12-01

    A direct sampling with organic solvent extracts for simultaneous multi-element determination implemented with inductively coupled plasma atomic emission spectrometry (ICP-AES) associated with a flow injection liquid-liquid extraction (FI-LLE) sample preconcentration method was studied. The "robustness" of the plasma discharge with tributyl phosphate (TBP) loading was diagnosed by using the Mg II 279.55 nm and Mg I 285.21 nm lines intensity ratio. A FI-LLE preconcentration system for rare earth elements (REEs)-nitrate-TBP was established by using a laboratory-designed phase separator. For these elements, an average sensitivity enhancement factor of 64 was obtained with respect to ICP-AES sampling with aqueous solutions. The precision of the method was characterized by a relative standard deviation (%RSD) of 1.8 - 5.2%. A throughput of 27 samples per hour can be achieved with an organic solvent consumption of less than 200 microl per determination. Good results were obtained for the analysis of standard reference materials.

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

    SciTech Connect

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

    2013-01-15

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

  12. Comparison of a portable micro-X-ray fluorescence spectrometry with inductively coupled plasma atomic emission spectrometry for the ancient ceramics analysis

    NASA Astrophysics Data System (ADS)

    Papadopoulou, D. N.; Zachariadis, G. A.; Anthemidis, A. N.; Tsirliganis, N. C.; Stratis, J. A.

    2004-12-01

    Two multielement instrumental methods of analysis, micro X-ray fluorescence spectrometry (micro-XRF) and inductively coupled plasma atomic emission spectrometry (ICP-AES) were applied for the analysis of 7th and 5th century B.C. ancient ceramic sherds in order to evaluate the above two methods and to assess the potential to use the current compact and portable micro-XRF instrument for the in situ analysis of ancient ceramics. The distinguishing factor of interest is that micro-XRF spectrometry offers the possibility of a nondestructive analysis, an aspect of primary importance in the compositional analysis of cultural objects. Micro-XRF measurements were performed firstly directly on the ceramic sherds with no special pretreatment apart from surface cleaning (micro-XRF on sherds) and secondly on pressed pellet disks which were prepared for each ceramic sherd (micro-XRF on pellet). For the ICP-AES determination of elements, test solutions were prepared by the application of a microwave-assisted decomposition procedure in closed high-pressure PFA vessels. Also, the standard reference material SARM 69 was used for the efficiency calibration of the micro-XRF instrument and was analysed by both methods. In order to verify the calibration, the standard reference materials NCS DC 73332 and SRM620 as well as the reference materials AWI-1 and PRI-1 were analysed by micro-XRF. Elemental concentrations determined by the three analytical procedures (ICP-AES, micro-XRF on sherds and micro-XRF on pellets) were statistically treated by correlation analysis and Student's t-test (at the 95% confidence level).

  13. Spontaneous emission from the atom stabilized by a strong high-frequency laser field

    NASA Astrophysics Data System (ADS)

    Bogatskaya, A. V.; Volkova, E. A.; Popov, A. M.

    2017-09-01

    The spontaneous emission of a quantum system driven by a high-intensity, high-frequency classical laser field is analyzed. The study is based on the accurate consideration of the quantum system interacting with vacuum-quantized field modes in the first order of perturbation theory, while the intense laser field is considered classically beyond this theory. It is demonstrated that the spectrum of the spontaneous emission can be used for analyzing the strong-field dynamics and the structure of the energy spectrum of an atomic system. In particular, it is found that in high-frequency fields (where the energy of the laser quanta is greater than the ionization potential) atoms manifest the features of the Kramers-Henneberger atom. It is also found that in the stabilization regime, the atom emits both odd and even laser radiation harmonics.

  14. Selective solid phase extraction of copper using a new Cu(II)-imprinted polymer and determination by inductively coupled plasma optical emission spectroscopy (ICP-OES).

    PubMed

    Yilmaz, Vedat; Arslan, Zikri; Hazer, Orhan; Yilmaz, Hayriye

    2014-05-01

    This work reports the preparation of a novel Cu(II)-ion imprinted polymer using 2-thiozylmethacrylamide (TMA) for on-line preconcentration of Cu(II) prior to its determination by inductively coupled optical emission spectroscopy (ICP-OES). Cu(II)-TMA monomer (complex) was synthesized and copolymerized via bulk polymerization method in the presence of ethyleneglycoldimethacrylate cross-linker. The resulting polymer was washed with 5% (v/v) HNO3 to remove Cu(II) ions and then with water until a neutral pH. The ion imprinted polymer was characterized by FT-IR and scanning electron microscopy. The experimental conditions were optimized for on-line preconcentration of Cu(II) using a minicolumn of ion imprinted polymer (IIP). Quantitative retention was achieved between pH 5.0 and 6.0, whereas the recoveries for the non-imprinted polymer (NIP) were about 61%. The IIP showed about 30 times higher selectivity to Cu(II) in comparison to NIP. The IIP also exhibited excellent selectivity for Cu(II) against the competing transition and heavy metal ions, including Cd, Co, Cr, Fe, Mn, Ni, Pb and Zn. Computational calculations revealed that the selectivity of IIP was mediated by the stability of Cu(II)-TMA complex which was far more stable than those of Co(II), Ni(II) and Zn(II) that have similar charge and ionic radii to Cu(II). A volume of 10 mL sample solution was loaded onto the column at 4.0 mL min(-1) by using a sequential injection system (FIALab 3200) followed by elution with 1.0 mL of 2% (v/v) HNO3. The relative standard deviation (RSD) and limit of detection (LOD, 3s) of the method were 3.2% and 0.4 μg L(-1), respectively. The method was successfully applied to determination of Cu(II) in fish otoliths (CRM 22), bone ash (SRM 1400) and coastal seawater and estuarine water samples.

  15. Selective solid phase extraction of copper using a new Cu(II)-imprinted polymer and determination by inductively coupled plasma optical emission spectroscopy (ICP-OES)

    PubMed Central

    Yilmaz, Vedat; Arslan, Zikri; Hazer, Orhan; Yilmaz, Hayriye

    2014-01-01

    This work reports the preparation of a novel Cu(II)-ion imprinted polymer using 2-thiozylmethacrylamide (TMA) for on-line preconcentration of Cu(II) prior to its determination by inductively coupled optical emission spectroscopy (ICP-OES). Cu(II)-TMA monomer (complex) was synthesized and copolymerized via bulk polymerization method in the presence of ethyleneglycoldimethacrylate cross-linker. The resulting polymer was washed with 5% (v/v) HNO3 to remove Cu(II) ions and then with water until a neutral pH. The ion imprinted polymer was characterized by FT-IR and scanning electron microscopy. The experimental conditions were optimized for on-line preconcentration of Cu(II) using a minicolumn of ion imprinted polymer (IIP). Quantitative retention was achieved between pH 5.0 and 6.0, whereas the recoveries for the non-imprinted polymer (NIP) were about 61%. The IIP showed about 30 times higher selectivity to Cu(II) in comparison to NIP. The IIP also exhibited excellent selectivity for Cu(II) against the competing transition and heavy metal ions, including Cd, Co, Cr, Fe, Mn, Ni, Pb and Zn. Computational calculations revealed that the selectivity of IIP was mediated by the stability of Cu(II)-TMA complex which was far more stable than those of Co(II), Ni(II) and Zn(II) that have similar charge and ionic radii to Cu(II). A volume of 10 mL sample solution was loaded onto the column at 4.0 mL min−1 by using a sequential injection system (FIALab 3200) followed by elution with 1.0 mL of 2% (v/v) HNO3. The relative standard deviation (RSD) and limit of detection (LOD, 3s) of the method were 3.2% and 0.4 μg L−1, respectively. The method was successfully applied to determination of Cu(II) in fish otoliths (CRM 22), bone ash (SRM 1400) and coastal seawater and estuarine water samples. PMID:24511158

  16. Developments in the application of gas chromatography with atomic emission (plus mass spectrometric) detection.

    PubMed

    van Stee, L L P; Brinkman, U A Th

    2008-04-04

    Capillary gas chromatography with atomic emission detection is a highly element-selective and sensitive detection technique for many non-metal as well as metallic elements. A 3-5 order of magnitude element/carbon selectivity, compound-independent calibration and the possibility to calculate (partial) molecular formulae are some of the attractive features of the technique. In the present review, the emphasis is on real-life applications for non-metals such as sulphur, phosphorus, nitrogen and the halogens, and on the potential of combined atomic emission/mass spectrometric detection.

  17. Some unique properties of gas chromatography coupled with atomic-emission detection.

    PubMed

    Andersson, Jan T

    2002-07-01

    The atomic-emission detector in gas chromatography is enormously versatile in applications in analytical chemistry. Its unique properties of high selectivity for most elements and low limits of detection combine to make it the preferred detector for many analytical problems. In this review the stress is laid on the possibility of using it for compound-independent calibration, for determination of the empirical formula of an unknown analyte, for isotope-selective detection, and on derivatization to give AED-active derivatives with advantageous detection properties. Both metals and non-metals are considered and examples of the use of atomic emission detection in real-world analysis are discussed.

  18. Single-Photon Emission of a Hydrogenlike Atom

    NASA Astrophysics Data System (ADS)

    Skobelev, V. V.

    2016-11-01

    Implementing a previously obtained, original solution of the Dirac equation for an electron in the field of a nucleus ( Ze) expressed in terms of the wave function of the corresponding Schrödinger equation and its derivatives in spherical coordinates and the spin projection operator Σ3 associated with the eigenfunction, taking into account in each component of the spinor the leading term of the expansion in the small parameter ( Zα), α = e 2 / ħc ≈ 1 / 137, the partial probabilities W of emission of a photon ( Zα)* → ( Zα) + γ have been calculated. Here two orthogonal states of the linear polarization of the photon, and also the spin states of the electron, which previously had not been taken into consideration, have been taken into account in the transverse gauge. It turns out that the probabilities W of emission of a photon per unit time for any allowed transitions are proportional to (Zα)4, as was previously accepted, and the selection rules for the quantum number m have the usual form ∆ m = 0,±1. It was found that a spin flip does not take place during emission. In contrast to the customary situation with the selection rules for the quantum number l being of the form ∆ l = ±1, for ∆ m = ±1 there also exist integrals over dcosθ which are not equal to zero for undetermined odd values of ∆ l. In this, and also in a fundamentally different dependence of the amplitude on the quantum numbers consist the differences from the traditional approach to the problem. Necessary conditions are formulated, under the fulfillment of which the selection rules for l are not changed, having values ∆ l = ±1 for arbitrary ∆ m, but it was not possible, however, to give a complete proof of these rules.

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

    PubMed

    Ma, Qianli; Dagdigian, Paul J

    2011-07-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1978-01-01

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

  1. Multielement plant tissue analysis using ICP spectrometry.

    PubMed

    Hansen, T H; de Bang, T C; Laursen, K H; Pedas, P; Husted, S; Schjoerring, J K

    2013-01-01

    Plant tissue analysis is a valuable tool for evaluating the nutritional status and quality of crops and is widely used for scientific and commercial purposes. The majority of plant analyzes are now performed by techniques based on ICP spectrometry such as inductively coupled plasma-optical emission spectroscopy (ICP-OES) or ICP-mass spectrometry (ICP-MS). These techniques enable fast and accurate measurements of multielement profiles when combined with appropriate methods for sample preparation and digestion. This chapter presents state-of-the-art methods for digestion of plant tissues and subsequent analysis of their multielement composition by ICP spectrometry. Details on upcoming techniques, expected to gain importance within the field of multielement plant tissue analysis over the coming years, are also provided. Finally, attention is given to laser ablation ICP-MS (LA-ICP-MS) for multielement bioimaging of plant tissues. The presentation of the methods covers instructions on all steps from sampling and sample preparation to data interpretation.

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

    SciTech Connect

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

    2008-03-29

    To analyze the local structure and/or chemical states of boron atoms in boron-doped diamond, which can be synthesized by the microwave plasma-assisted chemical vapor deposition method (CVD-B-diamond) and the temperature gradient method at high pressure and high temperature (HPT-B-diamond), we measured the soft X-ray emission spectra in the CK and BK regions of B-diamonds using synchrotron radiation at the Advanced Light Source (ALS). X-ray spectral analyses using the fingerprint method and molecular orbital calculations confirm that boron atoms in CVD-B-diamond substitute for carbon atoms in the diamond lattice to form covalent B-C bonds, while boron atoms in HPT-B-diamond react with the impurity nitrogen atoms to form hexagonal boron nitride. This suggests that the high purity diamond without nitrogen impurities is necessary to synthesize p-type B-diamond semiconductors.

  3. Chemical analysis of impurity boron atoms in diamond using soft X-ray emission spectroscopy.

    PubMed

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

    2008-07-01

    To analyze the local structure and/or chemical states of boron atoms in boron-doped diamond, which can be synthesized by the microwave plasma-assisted chemical vapor deposition method (CVD-B-diamond) and the temperature gradient method at high pressure and high temperature (HPT-B-diamond), we measured the soft X-ray emission spectra in the CK and BK regions of B-diamonds using synchrotron radiation at the Advanced Light Source (ALS). X-ray spectral analyses using the fingerprint method and molecular orbital calculations confirm that boron atoms in CVD-B-diamond substitute for carbon atoms in the diamond lattice to form covalent B-C bonds, while boron atoms in HPT-B-diamond react with the impurity nitrogen atoms to form hexagonal boron nitride. This suggests that the high purity diamond without nitrogen impurities is necessary to synthesize p-type B-diamond semiconductors.

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

    NASA Astrophysics Data System (ADS)

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

    2016-10-01

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

  5. Effects of atomic oxygen on OH Meinel emission bands in the MLT region

    NASA Astrophysics Data System (ADS)

    Von Savigny, Christian; Lednyts'kyy, Olexandr

    The OH Meinel airglow is one of the most prominent features of the terrestrial nightglow and has been employed for several decades to remotely sense the mesopause region. However, some aspects of the OH kinetics are still not fully understood. In this contribution we present recent results on the importance of quenching by atomic oxygen on the vertical distribution of different OH Meinel bands. OH Meinel emissions from different vibrational levels are known to occur at slightly different altitudes in the terrestrial airglow with emissions originating from higher vibrational levels peaking at higher altitudes. Our earlier model studies suggested quenching by atomic oxygen to be a principal cause of these vertical shifts. Here we employ the tropical mesopause region - characterized by pronounced semiannual variations - as a natural laboratory to test the hypothesis that vertical shifts between different OH Meinel bands are a consequence of quenching by atomic oxygen. Multiyear nighttime satellite measurements of OH(3-1) and OH(6-2) volume emission rate profiles and atomic oxygen with SCIAMACHY (Scanning Imaging Absorption Spectrometer for Atmospheric Chartography) on Envisat are used. The MLT atomic oxygen profiles are retrieved from measurements of the O(1S-1D) green line emission based on the accepted 2-step excitation scheme and a semi-empirical photochemical model. The results clearly demonstrate that vertical shifts between the OH bands investigated are indeed correlated with the amount of atomic oxygen in the upper mesosphere, corroborating the hypothesis that quenching by atomic oxygen is a driver for the vertical shifts between different OH Meinel bands.

  6. Atomic nuclei decay modes by spontaneous emission of heavy ions

    NASA Astrophysics Data System (ADS)

    Poenaru, D. N.; Ivaşcu, M.; Sndulescu, A.; Greiner, Walter

    1985-08-01

    The great majority of the known nuclides with Z>40, including the so-called stable nuclides, are metastable with respect to several modes of spontaneous superasymmetric splitting. A model extended from the fission theory of alpha decay allows one to estimate the lifetimes and the branching ratios relative to the alpha decay for these natural radioactivities. From a huge amount of systematic calculations it is concluded that the process should proceed with maximum intensity in the trans-lead nuclei, where the minimum lifetime is obtained from parent-emitted heavy ion combinations leading to a magic (208Pb) or almost magic daughter nucleus. More than 140 nuclides with atomic number smaller than 25 are possible candidates to be emitted from heavy nuclei, with half-lives in the range of 1010-1030 s: 5He, 8-10Be, 11,12B, 12-16C, 13-17N, 15-22O, 18-23F, 20-26Ne, 23-28Na, 23-30Mg, 27-32Al, 28-36Si, 31-39P, 32-42S, 35-45Cl, 37-47Ar, 40-49 K, 42-51. . .Ca, 44-53 Sc, 46-53Ti, 48-54V, and 49-55 Cr. The shell structure and the pairing effects are clearly manifested in these new decay modes.

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

    NASA Technical Reports Server (NTRS)

    Kelly, R. L.

    1979-01-01

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

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

    NASA Technical Reports Server (NTRS)

    Kelly, R. L.

    1979-01-01

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

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

    DOEpatents

    Braymen, Steven D.

    1996-06-11

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

  10. DYNAMICS OF ATOMIC AND MOLECULAR EMISSION FEATURES FROM NANOSECOND, FEMTOSECOND LASER AND FILAMENT PRODUCED PLASMAS

    SciTech Connect

    Harilal, Sivanandan S.; Yeak, J.; Brumfield, Brian E.; Phillips, Mark C.

    2016-08-08

    In this presentation, the persistence of atomic, and molecular emission features and its relation to fundamental properties (temperature and density) of ablation plumes generated using various irradiation methods (ns, fs, filaments) will be discussed in detail along with its implications for remote sensing applications.

  11. Inductively coupled plasma-atomic emission spectroscopy: The determination of trace impurities in uranium hexafluoride

    NASA Astrophysics Data System (ADS)

    Floyd, M. A.; Morrow, R. W.; Farrar, R. B.

    An analytical method has been developed for the determination of trace impurities in high-purity uranium hexafluoride using liquid-liquid extraction of the uranium from the trace impurities followed by analysis with inductively coupled plasma-atomic emission spectroscopy. Detection limits, accuracy, and precision data are presented.

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

    USGS Publications Warehouse

    Hopkins, D.M.

    1991-01-01

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

  13. Atomic Data and Emission Line Intensities for CA VII

    NASA Technical Reports Server (NTRS)

    Landi, E.; Bhatia, A. K.

    2003-01-01

    In the present work we calculate energy levels, transition probabilities and electron-ion collisional excitation rates for the 3s(sup 2)3p(sup 2), 3s3p(sup 3) and 3s(sup 2)3p3d configurations of the silicon-like ion Ca VII. The total number of intermediate coupling levels considered is 27. Collision strengths are calculated at seven incident electron energies: 8, 10, 15, 20, 30,40 and 60 Ry, using the Distorted Wave approximation and a 5-configuration model. Excitation rate coefficients are calculated by assuming a Maxwellian distribution of velocities and are used to calculate level populations and line emissivities under the assumption of statistical equilibrium. Line intensity ratios are calculated and compared with observed values measured from SERTS and SOHO/CDS spectra. The diagnostic potential of Ca VII is demonstrated, with particular emphasis on the possibility to measure the Ne/Ca relative abundance through simultaneous observations of Ca VII and N VI lines. Ca VII proves to be an excellent tool for the study of the FIP effect in the solar transition region.

  14. Direct Measurements of Terahertz Meta-atoms with Near-Field Emission of Terahertz Waves

    NASA Astrophysics Data System (ADS)

    Serita, Kazunori; Darmo, Juraj; Kawayama, Iwao; Murakami, Hironaru; Tonouchi, Masayoshi

    2017-09-01

    We present the direct measurements of terahertz meta-atoms, an elementary unit of metamaterials, by using locally generated terahertz waves in the near-field region. In contrast to a conventional far-field terahertz spectroscopy or imaging, our technique features the localized emission of coherent terahertz pulses on a sub-wavelength scale, which has a potential for visualizing details of dynamics of each meta-atom. The obtained data show the near-field coupling among the meta-atoms and the impact of the electric field distribution from the excited meta-atom to neighbor meta-atoms. The observable LC resonance response is enhanced with an increase of numbers of meta-atoms. Furthermore, our approach also has a potential for visualizing the individual mode of meta-atom at different terahertz irradiation spots. These data can help us to understand the important role of the meta-atom in metamaterials and develop the novel terahertz components and devices such as active terahertz metamaterial and compact, high-sensitive bio-sensor devices.

  15. Direct Measurements of Terahertz Meta-atoms with Near-Field Emission of Terahertz Waves

    NASA Astrophysics Data System (ADS)

    Serita, Kazunori; Darmo, Juraj; Kawayama, Iwao; Murakami, Hironaru; Tonouchi, Masayoshi

    2017-07-01

    We present the direct measurements of terahertz meta-atoms, an elementary unit of metamaterials, by using locally generated terahertz waves in the near-field region. In contrast to a conventional far-field terahertz spectroscopy or imaging, our technique features the localized emission of coherent terahertz pulses on a sub-wavelength scale, which has a potential for visualizing details of dynamics of each meta-atom. The obtained data show the near-field coupling among the meta-atoms and the impact of the electric field distribution from the excited meta-atom to neighbor meta-atoms. The observable LC resonance response is enhanced with an increase of numbers of meta-atoms. Furthermore, our approach also has a potential for visualizing the individual mode of meta-atom at different terahertz irradiation spots. These data can help us to understand the important role of the meta-atom in metamaterials and develop the novel terahertz components and devices such as active terahertz metamaterial and compact, high-sensitive bio-sensor devices.

  16. Direct determination of Cu by liquid cathode glow discharge-atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Lu, Quanfang; Yang, Shuxiu; Sun, Duixiong; Zheng, Jidong; Li, Yun; Yu, Jie; Su, Maogen

    2016-11-01

    In this study, a novel liquid cathode glow discharge-atomic emission spectrometry was developed for the direct determination of Cu in aqueous solutions, in which the glow discharge plasma was produced in the solution between the needle-like Pt cathode and the electrolyte around it. The effects of discharge voltage, solution pH, and the ionic surfactant cetyltrimethylammonium chloride (CTAC) on emission intensities were investigated. The limit of detection (LOD) of Cu was compared with those measured by closed-type electrolyte cathode discharge-atomic emission spectrometry (ELCAD-AES). The results showed that the optimal operation conditions are voltage of 135 V, a pH of 1, and addition of 0.15% CTAC. CTAC can enhance the emission intensity and lower the LOD of Cu I. The net intensity of atomic emission lines of Cu I at 324.8 nm with 0.15% CTAC improved by 1.5 fold, and the LODs of the Cu at 135 V with 0.15% CTAC and without CTAC are 0.019 and 0.234 mg L- 1, respectively. The analytical capability of Cu in this study is comparable to the closed-type ELCAD-AES, and it satisfied the recommended levels of Cu in the WHO standards for drinking-water quality. This technique can be effectively used for on-line monitoring of metal ions in aqueous samples.

  17. Comparison of ultrasonic and thermospray systems for high performance sample introduction to inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Conver, Timothy S.; Koropchak, John A.

    1995-06-01

    This paper describes detailed work done in our lab to compare analytical figures of merit for pneumatic, ultrasonic and thermospray sample introduction (SI) systems with three different inductively coupled plasma-atomic emission spectrometry (ICP-AES) instruments. One instrument from Leeman Labs, Inc. has an air path echelle spectrometer and a 27 MHz ICP. For low dissolved solid samples with this instrument, we observed that the ultrasonic nebulizer (USN) and fused silica aperture thermospray (FSApT) both offered similar LOD improvements as compared to pneumatic nebulization (PN), 14 and 16 times, respectively. Average sensitivities compared to PN were better for the USN, by 58 times, compared to 39 times for the FSApT. For solutions containing high dissolved solids we observed that FSApT optimized at the same conditions as for low dissolved solids, whereas USN required changes in power and gas flows to maintain a stable discharge. These changes degraded the LODs for USN substantially as compared to those utilized for low dissolved solid solutions, limiting improvement compared to PN to an average factor of 4. In general, sensitivities for USN were degraded at these new conditions. When solutions with 3000 μg/g Ca were analyzed, LOD improvements were smaller for FSApT and USN, but FSApT showed an improvement over USN of 6.5 times. Sensitivities compared to solutions without high dissolved solids were degraded by 19% on average for FSApT, while those for USN were degraded by 26%. The SI systems were also tested with a Varian Instruments Liberty 220 having a vacuum path Czerny-Turner monochromator and a 40 MHz generator. The sensitivities with low dissolved solids solutions compared to PN were 20 times better for the USN and 39 times better for FSApT, and LODs for every element were better for FSApT. Better correlation between relative sensitivities and anticipated relative analyte mass fluxes for FSApT and USN was observed with the Varian instrument. LOD

  18. Evaluation of sample preparation methods for the detection of total metal content using inductively coupled plasma optical emission spectrometry (ICP-OES) in wastewater and sludge

    NASA Astrophysics Data System (ADS)

    Dimpe, K. M.; Ngila, J. C.; Mabuba, N.; Nomngongo, P. N.

    Heavy metal contamination exists in aqueous wastes and sludge of many industrial discharges and domestic wastewater, among other sources. Determination of metals in the wastewater and sludge requires sample pre-treatment prior to analysis because of certain challenges such as the complexity of the physical state of the sample, which may lead to wrong readings in the measurement. This is particularly the case with low analyte concentration to be detected by the instrument. The purpose of this work was to assess and validate the different sample preparation methods namely, hot plate and microwave-assisted digestion procedures for extraction of metal ions in wastewater and sludge samples prior to their inductively coupled plasma optical emission spectrometric (ICP-OES) determination. For the extraction of As, Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn, three acid mixtures, that is, HNO3/H2O2, HNO3/HClO4/H2O2 and aqua regia + H2O2, were evaluated. Influent wastewater spiked with the SRM (CWW-TM-B) was used for the optimization of acid mixtures affecting the extraction procedure. After sample digestion, the filtration capabilities of cellulose-acetate filter paper and the acrodisc syringe filter with the pore size of 0.45 μm were compared. In terms of performance, acrodisc syringe filter in terms of the improved recoveries obtained, was found to be the best filtration method compared to the filter paper. Based on the analytical results obtained, microwave-assisted digestion (MAD) using aqua regia + H2O2 mixture was found to be the most suitable method for extraction of heavy metals and major elements in all the sample matrices. Therefore, MAD using aqua regia + H2O2 mixture was used for further investigations. The precision of the developed MAD method expressed in terms of relative standard deviations (% RSD) for different metals was found to be <5%. The limits of detection (LOD) and limits of quantification (LOQ) ranged from 0.12% to 2.18 μg L-1 and 0.61% to 3.43 μg L-1

  19. Separation techniques for the clean-up of radioactive mixed waste for ICP-AES/ICP-MS analysis

    SciTech Connect

    Swafford, A.M.; Keller, J.M.

    1993-03-17

    Two separation techniques were investigated for the clean-up of typical radioactive mixed waste samples requiring elemental analysis by Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) or Inductively Coupled Plasma-Mass Spectrometry (ICP-MS). These measurements frequently involve regulatory or compliance criteria which include the determination of elements on the EPA Target Analyte List (TAL). These samples usually consist of both an aqueous phase and a solid phase which is mostly an inorganic sludge. Frequently, samples taken from the waste tanks contain high levels of uranium and thorium which can cause spectral interferences in ICP-AES or ICP-MS analysis. The removal of these interferences is necessary to determine the presence of the EPA TAL elements in the sample. Two clean-up methods were studied on simulated aqueous waste samples containing the EPA TAL elements. The first method studied was a classical procedure based upon liquid-liquid extraction using tri-n- octylphosphine oxide (TOPO) dissolved in cyclohexane. The second method investigated was based on more recently developed techniques using extraction chromatography; specifically the use of a commercially available Eichrom TRU[center dot]Spec[trademark] column. Literature on these two methods indicates the efficient removal of uranium and thorium from properly prepared samples and provides considerable qualitative information on the extraction behavior of many other elements. However, there is a lack of quantitative data on the extraction behavior of elements on the EPA Target Analyte List. Experimental studies on these two methods consisted of determining whether any of the analytes were extracted by these methods and the recoveries obtained. Both methods produced similar results; the EPA target analytes were only slightly or not extracted. Advantages and disadvantages of each method were evaluated and found to be comparable.

  20. Analytical control of wollastonite for biomedical applications by use of atomic absorption spectrometry and inductively coupled plasma atomic emission spectrometry.

    PubMed

    De Aza, P N; Guitián, F; De Aza, S; Valle, F J

    1998-04-01

    Preliminary in vitro experiments revealed that wollastonite (CaSiO3) is a potentially highly bioactive material that forms a hyroxyapatite (HA) surface layer on exposure to simulated body fluid with an ion concentration, pH and temperature virtually identical with those of human blood plasma. The formation of the HA layer is an essential requirement for an artificial material to be used as bioactive bone substitute. This finding opens up a wide field for biomedical applications of wollastonite. Biomaterials used as implants in the human body require strict control of trace elements and of the toxic species specified in American Society for Testing and Materials F-1185-88 (As, Cd, Hg and Pb) in ceramic hydroxyapatite for surgical implantation. In this work, two types of pseudowollastonite, the high temperature form of wollastonite, were analysed by using cold vapour atomic absorption spectrometry and hydride generation atomic absorption spectrometry, in order to determine the elements stated in the above-mentioned norm, and inductively coupled plasma atomic emission spectrometry to establish the SiO2/CaO ratio of the two materials and analyse for all other impurities introduced by the raw materials and by the processes of synthesis, sintering and grinding. Barium and Mg were especially prominent in raw materials, and Zr, Y, Mg, W, Co and Ni come mainly from the processing.

  1. [Research on the atomic emission spectroscopy of atmospheric pressure plasma process].

    PubMed

    Jin, Jiang; Li, Na; Xu, Lu; Wang, Bo; Jin, Hui-Liang

    2013-02-01

    In the reaction of the atmospheric pressure plasma process, the heat stable process of the atmospheric pressure plasma jet has a direct impact on the removal rate, CF4 is the provider of active F* atom, O2 is important auxiliary gas, and they play an important role in the process. In order to research the rule of the concentration of the 3 parameters upon the atmospheric pressure plasma processing, the atmospheric pressure plasma jet was used for processing and the spectrometer was used to monitor the changes in the process. The experiment indicates that: when the heat is stable, the concentration of the active F* atom essentially remains unchanged; with increasing the concentration of gas CF4, the spectrum of the active F* atom has self-absorption phenomena, so using the atomic emission spectroscopy method to monitor the changes in the concentration of active F* atom generated by CF4 is not completely exact; because O2 can easily react with the dissociation product of CF4, which inhibits the compound of the active F* atom, so in a certain range with increasing the concentration of gas O2, the concentration of the active F* atom becomes strong.

  2. Spectral Emission of fast non-Maxwellian Atoms at metallic Surfaces in low density Plasmas

    NASA Astrophysics Data System (ADS)

    Dickheuer, Sven; Marchuk, Oleksandr; Brandt, Christian; Pospieszczyk, Albrecht

    2016-09-01

    We have observed Doppler shifted components of the Balmer-lines emitted by fast non-Maxwellian atoms using different targets in a linear magnetized plasma in the PSI-2 device. In a pure hydrogen plasma the Doppler shifted components of the Balmer emission lines cannot be detected above the signal-to-noise-ratio. However, in a mixed H/Ar plasma with composition of 1:1 the Doppler red- and blue-shifted components can be clearly observed. The Balmer-lines are analyzed by optical emission spectroscopy at observations angles of 35° and 90°. For target materials we use Ag, Pd, Fe and C. An acceleration potential can be applied to the target to change the kinetic energy of the incoming ions between 40 and 200 eV enabling the observation of the Doppler shifted components. The emission mechanism is discussed in details and is probably due to excitation transfer from metastable argon atoms to the fast hydrogen atoms. The Doppler shifted signal can be used to determine the properties of the surfaces, e.g., the energy and angular distribution of reflected atoms. Also the spectral reflectance of the target surface can be obtained and tested against the reference data and measurements with light calibration sources.

  3. Angle-resolved 2D imaging of electron emission processes in atoms and molecules

    SciTech Connect

    Kukk, E.; Wills, A.A.; Langer, B.; Bozek, J.D.; Berrah, N.

    2004-09-02

    A variety of electron emission processes have been studied in detail for both atomic and molecular systems, using a highly efficient experimental system comprising two time-of-flight (TOF) rotatable electron energy analyzers and a 3rd generation synchrotron light source. Two examples are used here to illustrate the obtained results. Firstly, electron emissions in the HCL molecule have been mapped over a 14 eV wide photon energy range over the Cl 2p ionization threshold. Particular attention is paid to the dissociative core-excited states, for which the Auger electron emission shows photon energy dependent features. Also, the evolution of resonant Auger to the normal Auger decay distorted by post-collision interaction has been observed and the resonating behavior of the valence photoelectron lines studied. Secondly, an atomic system, neon, in which excitation of doubly excited states and their subsequent decay to various accessible ionic states has been studied. Since these processes only occurs via inter-electron correlations, the many body dynamics of an atom can be probed, revealing relativistic effects, surprising in such a light atom. Angular distribution of the decay of the resonances to the parity unfavored continuum exhibits significant deviation from the LS coupling predictions.

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

    SciTech Connect

    Jen, H.H.

    2015-09-15

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

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

    PubMed Central

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

    2016-01-01

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

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

    PubMed

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

    2016-01-14

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

  7. Electron ionization of metastable nitrogen and oxygen atoms in relation to the auroral emissions

    NASA Astrophysics Data System (ADS)

    Pandya, Siddharth; Joshipura, K. N.

    Atomic and molecular excited metastable states (EMS) are exotic systems due to their special properties like long radiative life-time, large size (average radius) and large polarizability along with relatively smaller first ionization energy compared to their respective ground states (GS). The present work includes our theoretical calculations on electron impact ionization of metastable atomic states N( (2) P), N( (2) D) of nitrogen and O( (1) S), O( (1) D) of oxygen. The targets of our present interest, are found to be present in our Earth's ionosphere and they play an important role in auroral emissions observed in Earth’s auroral regions [1] as also in the emissions observed from cometary coma [2, 3] and airglow emissions. In particular, atomic oxygen in EMS can radiate, the visible O( (1) D -> (3) P) doublet 6300 - 6364 Å red doublet, the O( (1) S -> (1) D) 5577 Å green line, and the ultraviolet O( (1) S -> (3) P) 2972 Å line. For metastable atomic nitrogen one observes the similar emissions, in different wavelengths, from (2) D and (2) P states. At the Earth's auroral altitudes, from where these emissions take place in the ionosphere, energetic electrons are also present. In particular, if the metastable N as well as O atoms are ionized by the impact of electrons then these species are no longer available for emissions. This is a possible loss mechanism, and hence it is necessary to analyze the importance of electron ionization of the EMS of atomic O and N, by calculating the relevant cross sections. In the present paper we investigate electron ionization of the said metastable species by calculating relevant total cross sections. Our quantum mechanical calculations are based on projected approximate ionization contribution in the total inelastic cross sections [4]. Detailed results and discussion along with the significance of these calculations will be presented during the COSPAR-2014. References [1] A.Bhardwaj, and G. R. Gladstone, Rev. Geophys., 38

  8. Characteristics of krypton ion emission from a gas field ionization source with a single atom tip

    NASA Astrophysics Data System (ADS)

    Shichi, Hiroyasu; Matsubara, Shinichi; Hashizume, Tomihiro

    2017-06-01

    A scanning ion beam instrument equipped with a gas field ionization source (GFIS) has been commercialized, but only helium and neon are currently available as GFISs. The characteristics of krypton ion emission from a single atom tip (SAT) have not been reported yet. In this study, the characteristics of krypton ion emission were investigated by field ion microscopy. At 65 K, the krypton ion emission current reached approximately 40 pA, which is 1 order of magnitude higher than that at 130 K. As the krypton gas pressure was increased, the krypton ion current increased. At a pressure of 0.3 Pa, the emission current was anticipated to reach 200 pA, which may be high enough for nanofabrication. The variation of the krypton ion current was as low as 5% in one hour. We concluded that a krypton ion beam instrument equipped with a GFIS will be a powerful tool for nanofabrication.

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

    SciTech Connect

    Fara, M.; Novak, F.

    1995-12-01

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

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

    SciTech Connect

    1998-02-15

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

  11. Automated diagnostics of a magnetron discharge plasma based on atomic molecular emission spectra

    NASA Astrophysics Data System (ADS)

    Gradov, V. M.; Zimin, A. M.; Krivitskiy, S. E.; Serushkin, S. V.; Troynov, V. I.

    2012-12-01

    A software-hardware complex intended for investigating spatial distributions of the plasma spectral emissivity is described. It allows us to record and identify the lines and systems of molecular bands in an automatic mode and to perform computer processing of spectra. Molecular bands of deuterium for different electronic-vibrational-rotational transitions are identified. The excitation temperatures of atomic levels, translational, rotational and vibrational temperatures are estimated for a discharge in a planar magnetron.

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

    DOEpatents

    Braymen, S.D.

    1996-06-11

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

  13. On-line collection/concentration and determination of transition and rare-earth metals in water samples using Multi-Auto-Pret system coupled with inductively coupled plasma-atomic emission spectrometry.

    PubMed

    Katarina, Rosi Ketrin; Oshima, Mitsuko; Motomizu, Shoji

    2009-05-15

    On-line preconcentration and determination of transition and rare-earth metals in water samples was performed using a Multi-Auto-Pret system coupled with inductively coupled plasma-atomic emission spectrometry (ICP-AES). The Multi-Auto-Pret AES system proposed here consists of three Auto-Pret systems with mini-columns that can be used for the preconcentration of trace metals sequentially or simultaneously, and can reduce analysis time to one-third and running cost of argon gas and labor. A newly synthesized chelating resin, ethylenediamine-N,N,N'-triacetate-type chitosan (EDTriA-type chitosan), was employed in the Multi-Auto-Pret system for the collection of trace metals prior to their measurement by ICP-AES. The proposed resin showed very good adsorption ability for transition and rare-earth metal ions without any interference from alkali and alkaline-earth metal ions in an acidic media. For the best result, pH 5 was adopted for the collection of metal ions. Only 5 mL of samples could be used for the determination of transition metals, while 20 mL of samples was necessary for the determination of rare-earth metals. Metal ions adsorbed on the resin were eluted using 1.5 M nitric acid, and were measured by ICP-AES. The proposed method was evaluated by the analysis of SLRS-4 river water reference materials for trace metals. Good agreement with certified and reference values was obtained for most of the metals examined; it indicates that the proposed method using the newly synthesized resin could be favorably used for the determination of transition and rare-earth metals in water samples by ICP-AES.

  14. Decoherence by spontaneous emission: A single-atom analog of superradiance

    NASA Astrophysics Data System (ADS)

    Souza, Reinaldo de Melo e.; Impens, François; Neto, Paulo A. Maia

    2016-12-01

    We show that the decoherence of the atomic center-of-mass induced by spontaneous emission involves interferences corresponding to a single-atom analog of superradiance. We use a decomposition of the stationary decoherence rate as a sum of local and nonlocal contributions obtained to second order in the interaction by the influence functional method. These terms are respectively related to the strength of the coupling between system and environment, and to the quality of the information about the system leaking into the environment. While the local contribution always yields a positive decoherence rate, the nonlocal one may lead to recoherence when only partial information about the system is obtained from the disturbed environment. The nonlocal contribution contains interferences between different quantum amplitudes leading to oscillations of the decoherence rate reminiscent of superradiance. These concepts, illustrated here in the framework of atom interferometry within a trap, may be applied to a variety of quantum systems.

  15. Capacitively coupled microwave plasma atomic emission spectrometer for the determination of lead in whole blood.

    PubMed

    Wensing, M W; Smith, B W; Winefordner, J D

    1994-02-15

    The determination of lead in whole blood by atomic emission spectrometry using a capacitively coupled microwave plasma and a tungsten filament electrode is presented. When the plasma-supporting electrode is also used as the sample holder, transfer of the sample to the plasma is 100%. Microwaves are used to dry the sample and, at higher powers, ignite a helium plasma which results in the atomization and excitation of Pb. Using this methodology, a detection limit of 3 pg of Pb was obtained using 5-microL aqueous samples. The precision was 9%. Whole blood samples were subjected to a drying stage similar to that of the aqueous samples. Following this drying stage, a low-power (30 W) helium plasma was ignited and used to ash the blood sample. Higher power plasmas (> 150 W) were used to atomize and excite the Pb. Recovery of Pb from the blood samples was 88%, when compared to aqueous standards.

  16. Pulsed cooperative backward emissions from non-degenerate atomic transitions in sodium

    NASA Astrophysics Data System (ADS)

    Thompson, Jonathan V.; Ballmann, Charles W.; Cai, Han; Yi, Zhenhuan; Rostovtsev, Yuri V.; Sokolov, Alexei V.; Hemmer, Phillip; Zheltikov, Aleksei M.; Ariunbold, Gombojav O.; Scully, Marlan O.

    2014-10-01

    We study backward cooperative emissions from a dense sodium atomic vapor. Ultrashort pulses produced from a conventional amplified femtosecond laser system with an optical parametric amplifier are used to excite sodium atoms resonantly on the two-photon 3S1/2-4S1/2 transition. Backward superfluorescent emissions (BSFEs), both on the 4S1/2-3P3/2 and 4S1/2-3P1/2 transitions, are observed. The picosecond temporal characteristics of the BSFE are observed using an ultrafast streak camera. The power laws for the dependencies of the average time delay and the intensity of the BSFEs on input power are analyzed in the sense of cooperative emission from nonidentical atomic species. As a result, an absolute (rather than relative) time delay and its fluctuations (free of any possible external noise) are determined experimentally. The possibility of a backward swept-gain superfluorescence as an artificial laser guide star in the sodium layer in the mesosphere is also discussed.

  17. On the Effect of Photoinduced Emission of Alkali Atoms from a Paraffin Coating on the Rate of Spin Relaxation of Atoms in the Volume of a Cell

    SciTech Connect

    Aleksandrov, E.B.; Balabas, M.V.

    2005-06-15

    The effect of photoinduced emission of alkali atoms from the paraffin coating of a cell on the spin relaxation time of the atoms was studied experimentally. No effect was detected. It was additionally found that long irradiation of the cell surface by light with a power density of about 1 mW/cm{sup 2} does not cause any degradation of the coating in spite of almost complete removal of the atoms from the coating due to their photostimulated diffusion in the layer and photodesorption. After the irradiation is complete, the surface contacting with the alkali vapor is again saturated with the alkali atoms with a time constant of about 1 h.

  18. Optimized microwave-assisted decomposition method for multi-element analysis of glass standard reference material and ancient glass specimens by inductively coupled plasma atomic emission spectrometry.

    PubMed

    Zachariadis, G; Dimitrakoudi, E; Anthemidis, A; Stratis, J

    2006-02-28

    A novel microwave-assisted wet-acid decomposition method for the multi-element analysis of glass samples using inductively coupled plasma atomic emission spectrometry (ICP-AES) was developed and optimized. The SRM 621 standard reference glass material was used for this purpose, because it has similar composition with either archaeological glass specimens or common modern glasses. For the main constituents of SRM 621 (Ca, Na, Al, Fe, Mg, Ba and Ti), quality control data are given for all the examined procedures. The chemical and instrumental parameters of the method were thoroughly optimized. Thirteen acid mixtures of hydrochloric, nitric, and hydrofluoric acids in relation to two different microwave programs were examined in order to establish the most efficient protocol for the determination of metals in glass matrix. For both microwave programs, an intermediate step was employed with addition of H(3)BO(3) in order to compensate the effect of HF, which was used in all protocols. The suitability of the investigated protocols was evaluated for major (Ca, Na, Al), and minor (Fe, Mg, Ba, Ti, Mn, Cu, Sb, Co, Pb) glass constituents. The analytes were determined using multi-element matrix matched standard solutions. The analytical data matrix was processed chemometrically in order to evaluate the examined protocols in terms of their accuracy, precision and sensitivity, and eventually select the most efficient method for ancient glass. ICP-AES parameters such as spectral line, RF power and sample flow rate were optimized using the proposed protocol. Finally, the optimum method was successfully applied to the analysis of a number of ancient glass fragments.

  19. The detection of salivary minerals in smokers and non-smokers with chronic periodontitis by the inductively coupled plasma-atomic emission spectrophotometry technique.

    PubMed

    Erdemir, Ebru Olgun; Erdemir, Ali

    2006-06-01

    The purpose of this study was to evaluate the effect of smoking on the salivary minerals in subjects with chronic periodontitis by the inductively coupled plasma-atomic emission spectrophotometry (ICP-AES) technique. The study group included 24 subjects-12 smokers and 12 non-smokers-with chronic periodontitis. Clinical measurements and non-stimulated whole saliva were obtained, and the levels of five elements-sodium, potassium, calcium, magnesium, and phosphate-in each specimen were analyzed. When the clinical parameters were compared between groups, only plaque index was significantly higher in smokers than non-smokers (P <0.05). The mean plaque index of smokers and non-smokers was 1.93 +/- 0.51 and 1.51 +/- 0.39, respectively. The results of this study showed that there were no significant differences between groups in the mineral content of saliva. In smokers, there were positive correlations between the levels of calcium, sodium, and magnesium and clinical attachment level. There was also a positive correlation between the level of phosphate and the percentage of bleeding on probing. In non-smokers, there was a negative correlation only between the mean level of sodium and plaque index (P <0.05). The present study showed that no significant differences were found between the mineral content of saliva of smokers and non-smokers by the ICP-AES technique. It is a useful, fast, and sensitive technique compared to other techniques, and it can be advised for researchers while analyzing the mineral content of saliva.

  20. ICP0 Antagonizes ICP4-Dependent Silencing of the Herpes Simplex Virus ICP0 Gene

    PubMed Central

    Liu, Mingyu; Rakowski, Brandon; Gershburg, Edward; Weisend, Carla M.; Lucas, Olivier; Schmidt, Edward E.; Halford, William P.

    2010-01-01

    ICP0 is a regulatory protein that plays a critical role in the replication-latency balance of herpes simplex virus (HSV). Absence of ICP0 renders HSV prone to establish quiescent infections, and thus cellular repressor(s) are believed to silence HSV mRNA synthesis when ICP0 fails to accumulate. To date, an ICP0-antagonized repressor has not been identified that restricts HSV mRNA synthesis by more than 2-fold. We report the unexpected discovery that HSV's major transcriptional regulator, ICP4, meets the criteria of a bona fide ICP0-antagonized repressor of viral mRNA synthesis. Our study began when we noted a repressive activity that restricted ICP0 mRNA synthesis by up to 30-fold in the absence of ICP0. When ICP0 accumulated, the repressor only restricted ICP0 mRNA synthesis by 3-fold. ICP4 proved to be necessary and sufficient to repress ICP0 mRNA synthesis, and did so in an ICP4-binding-site-dependent manner. ICP4 co-immunoprecipitated with FLAG-tagged ICP0; thus, a physical interaction likely explains how ICP0 antagonizes ICP4's capacity to silence the ICP0 gene. These findings suggest that ICP0 mRNA synthesis is differentially regulated in HSV-infected cells by the virus-encoded repressor activity embedded in ICP4, and a virus-encoded antirepressor, ICP0. Bacteriophage λ relies on a similar repression-antirepression regulatory scheme to “decide” whether a given infection will be productive or silent. Therefore, our findings appear to add to the growing list of inexplicable similarities that point to a common evolutionary ancestry between the herpesviruses and tailed bacteriophage. PMID:20098619

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

    SciTech Connect

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

    2013-01-01

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

  2. Spontaneous emission and level shifts in absorbing disordered dielectrics and dense atomic gases: A Green's-function approach

    NASA Astrophysics Data System (ADS)

    Fleischhauer, Michael

    1999-09-01

    Spontaneous emission and Lamb shift of atoms in absorbing dielectrics and dense atomic gases are discussed using a microscopic Green's-function approach. Uncorrelated and random atomic positions are assumed, and the associated unphysical interactions between different atoms at the same location are eliminated (local field correction). For the case of an atom in a purely dispersive medium, the spontaneous-emission rate is altered by the well-known Lorentz local-field factor. When the mean distance between atoms becomes less than the resonance wavelength, results different from previously suggested expressions are found. In particular, it is shown that nearest-neighbor interactions become important. The results suggest that, for large densities, absorbing disordered dielectrics cannot accurately be described by a macroscopic approach that neglects correlations between atomic positions.

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

    SciTech Connect

    Ombaba, J.M.

    1992-01-01

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

  4. Interaction of vacuum ultraviolet excimer laser radiation with fused silica: II. Neutral atom and molecule emission

    SciTech Connect

    George, Sharon R.; Langford, S. C.; Dickinson, J. T.

    2010-02-15

    We report mass-resolved time-of-flight measurements of neutral Si, O, and SiO from ultraviolet-grade fused silica during pulsed 157-nm irradiation at fluences well below the threshold for optical breakdown. Although the emission intensities are strongly affected by thermal treatments that affect the density of strained bonds in the lattice, they are not consistently affected by mechanical treatments that alter the density of point defects, such as polishing and abrasion. We propose that the absorption of single 157 nm photons cleave strained bonds to produce defects that subsequently diffuse to the surface. There they react with dangling bonds to release neutral atoms and molecules. Hartree-Fock calculations on clusters containing these defects support the contention that defect interactions can yield emission. More direct emission by the photoelectronic excitation of antibonding chemical states is also supported.

  5. Study of atomic oxygen greenline dayglow emission in thermosphere during geomagnetic storm conditions

    NASA Astrophysics Data System (ADS)

    Bag, T.; Singh, Vir; Sunil Krishna, M. V.

    2017-01-01

    The influence of geomagnetic storms on the atomic oxygen greenline (557.7 nm) dayglow emission in thermosphere is studied during solar active and solar quiet conditions. This study is primarily based on the photochemical model with inputs obtained from experimental observations and empirical models. The updated rate coefficients, quantum yields and related cross-sections have been used from experimental results and theoretical studies. This study is presented for a low latitude station Tirunelveli (8.7°N, 77.8°E), India. The volume emission rate (VER) has been calculated using densities and temperatures from the empirical models. The modeled VER shows a positive correlation with the Dst index. The VER also shows a negative correlation with the number densities of O, O2, and N2. The VER, calculated at peak emission altitude, exhibits depletion during the main phase of the storm. The altitude of peak emission rate is unaffected by the geomagnetic storm activity. The study also reveals that the peak emission altitude depends on the F10.7 solar index. The peak emission altitude moves upward as the value of F10.7 solar index increases.

  6. Mapping Copper and Lead Concentrations at Abandoned Mine Areas Using Element Analysis Data from ICP-AES and Portable XRF Instruments: A Comparative Study.

    PubMed

    Lee, Hyeongyu; Choi, Yosoon; Suh, Jangwon; Lee, Seung-Ho

    2016-03-30

    Understanding spatial variation of potentially toxic trace elements (PTEs) in soil is necessary to identify the proper measures for preventing soil contamination at both operating and abandoned mining areas. Many studies have been conducted worldwide to explore the spatial variation of PTEs and to create soil contamination maps using geostatistical methods. However, they generally depend only on inductively coupled plasma atomic emission spectrometry (ICP-AES) analysis data, therefore such studies are limited by insufficient input data owing to the disadvantages of ICP-AES analysis such as its costly operation and lengthy period required for analysis. To overcome this limitation, this study used both ICP-AES and portable X-ray fluorescence (PXRF) analysis data, with relatively low accuracy, for mapping copper and lead concentrations at a section of the Busan abandoned mine in Korea and compared the prediction performances of four different approaches: the application of ordinary kriging to ICP-AES analysis data, PXRF analysis data, both ICP-AES and transformed PXRF analysis data by considering the correlation between the ICP-AES and PXRF analysis data, and co-kriging to both the ICP-AES (primary variable) and PXRF analysis data (secondary variable). Their results were compared using an independent validation data set. The results obtained in this case study showed that the application of ordinary kriging to both ICP-AES and transformed PXRF analysis data is the most accurate approach when considers the spatial distribution of copper and lead contaminants in the soil and the estimation errors at 11 sampling points for validation. Therefore, when generating soil contamination maps for an abandoned mine, it is beneficial to use the proposed approach that incorporates the advantageous aspects of both ICP-AES and PXRF analysis data.

  7. Balmer alpha emission and hydrogen atom energy in ion-source discharges

    SciTech Connect

    McNeill, D.H.; Kim, J.

    1981-07-01

    The structure of the hydrogen Balmer alpha line emission profiles from three types of neutral beam injector ion source plasmas (filling pressure approx. 10 mTorr, electron density approx. 1 to 2 x 10/sup 12/ cm/sup -3/, electron temperature approx. 2 to 4 eV) is studied with the aid of a simple model for the neutral particle balance and H/sub ..cap alpha../ emission. A large fraction of the H/sub ..cap alpha../ is produced by dissociative excitation of H/sub 2/ and dissociative recombination of H/sub 2//sup +/, while the remainder is produced by excitation of H atoms, most of which have energies that are close to the characteristic H/sub 2/ dissociation energies. The H/sub ..cap alpha../ linewidth is thus insensitive to the discharge operating conditions and equals approx. 0.27 A when only slow (approx. 0.3 eV) dissociatively excited atoms are present or approx. 0.35 A when fast (> 1 eV) atoms, apparently also produced in dissociation reactions, are present as well.

  8. Real-time emission spectrum from a hybrid atom-optomechanical cavity

    NASA Astrophysics Data System (ADS)

    Mirza, Imran

    Hybrid quantum systems are promising candidates for opening new avenues for quantum technologies [G. Kurizki et. al, PNAS, 112 (13), 3866-3873 (2015)]. Hybrid atom-optomechanical (HAOM) systems set an intriguing example in this context. From the perspective of practical utilizations of these HAOM systems in future quantum devices, it is crucial to fully understand the excitation dynamics as well as the spectral features of these systems. In this poster, I'll present my calculations of single-photon time-dependent (TD) spectrum emitted by such a HAOM system in a strong atom-cavity as well as strong cavity-mechanics (strong-strong) coupling regime [``Real-time emission spectrum from a hybrid atom-optomechanical cavity'', Imran M. Mirza, J. Opt. Soc. Am. B, 32 (8), 1604-1614 (2015)]. In order to make the system more realistic the effects of dissipation through the mechanical oscillator, optical cavity and spontaneous emission from the two-level emitter are also incorporated. The TD spectrum reveals some novel features that are not possible to observe otherwise. For instance, time order in which different side bands appears which explains different photon-phonon interactions responsible for the production of distinct spectral resonances. .

  9. Influence of Helium Atoms Absorption on the Emission Properties of Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Umaev, S. M.; Levchenko, A. A.; Kolesnikov, N. N.; Filatov, S. V.

    2017-04-01

    We investigated the emission properties of charge sources based on carbon nanotubes prepared by arc discharge deposition of nanotubes onto a flat copper substrate (Borisenko et al. in Instrum Exp Tech 57(6):755, 2014; Low Temp Phys 41(7):567, 2015). The charge sources were submerged into superfluid helium at temperature T=1.3 K. The collector fixed above the charge source at a distance of 0.3 mm was connected to an electrometer. The current of charges was measured by the electrometer when a high voltage was applied to the charge source. In the originally prepared source, the emission of charges (electrons) on the level of 10^{-10}A is observed at a negative voltage above U=80 V and increases with increasing voltage. If the source of charge was kept in liquid helium for 15 h, the current-voltage characteristic changed significantly. The current of charges on the same level of 10^{-10} A was registered at a voltage of U=150 V. Extraction of gases from the source placed in a vacuum chamber at room temperature for 48 h leads to the complete recovery of the emission properties. One can assume that the degradation of the emission properties of the sources is associated with the adsorption of helium atoms by carbon nanotubes at low temperatures. We did not observe any degradation of the emission properties of the charge sources in the case of positive charges injection into superfluid helium.

  10. 40 CFR Appendix C to Part 136 - Inductively Coupled Plasma-Atomic Emission Spectrometric Method for Trace Element Analysis of...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 23 2011-07-01 2011-07-01 false Inductively Coupled Plasma-Atomic... to Part 136—Inductively Coupled Plasma—Atomic Emission Spectrometric Method for Trace Element... technique. Samples are nebulized and the aerosol that is produced is transported to the plasma torch where...

  11. ICP-MS Workshop

    SciTech Connect

    Carman, April J.; Eiden, Gregory C.

    2014-11-01

    This is a short document that explains the materials that will be transmitted to LLNL and DNN HQ regarding the ICP-MS Workshop held at PNNL June 17-19th. The goal of the information is to pass on to LLNL information regarding the planning and preparations for the Workshop at PNNL in preparation of the SIMS workshop at LLNL.

  12. Association between ICP pulse waveform morphology and ICP B waves.

    PubMed

    Kasprowicz, Magdalena; Bergsneider, Marvin; Czosnyka, Marek; Hu, Xiao

    2012-01-01

    The study aimed to investigate changes in the shape of ICP pulses associated with different patterns of the ICP slow waves (0.5-2.0 cycles/min) during ICP overnight monitoring in hydrocephalus. Four patterns of ICP slow waves were characterized in 44 overnight ICP recordings (no waves - NW, slow symmetrical waves - SW, slow asymmetrical waves - AS, slow waves with plateau phase - PW). The morphological clustering and analysis of ICP pulse (MOCAIP) algorithm was utilized to calculate a set of metrics describing ICP pulse morphology based on the location of three sub-peaks in an ICP pulse: systolic peak (P(1)), tidal peak (P(2)) and dicrotic peak (P(3)). Step-wise discriminant analysis was applied to select the most characteristic morphological features to distinguish between different ICP slow waves. Based on relative changes in variability of amplitudes of P(2) and P(3) we were able to distinguish between the combined groups NW + SW and AS + PW (p < 0.000001). The AS pattern can be differentiated from PW based on respective changes in the mean curvature of P(2) and P(3) (p < 0.000001); however, none of the MOCAIP feature separates between NW and SW. The investigation of ICP pulse morphology associated with different ICP B waves may provide additional information for analysing recordings of overnight ICP.

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

    NASA Astrophysics Data System (ADS)

    Ombaba, Jackson M.

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

  14. Influence of spontaneous emission on a single-state atom interferometer

    NASA Astrophysics Data System (ADS)

    Beattie, S.; Barrett, B.; Weel, M.; Chan, I.; Mok, C.; Cahn, S. B.; Kumarakrishnan, A.

    2008-01-01

    We have studied the effects of spontaneous emission (SE) on a single-state time domain atom interferometer (AI) that uses trapped Rb atoms. The AI uses two standing wave pulses separated by time T to produce an echo signal at time 2T due to interference between momentum states. We find that SE influences both the shape of the echo signal and its periodic time-dependent amplitude in a manner consistent with theoretical predictions. The results show that the time-dependent signal from the AI is related to the effective radiative decay rate of the excited state. We also present results that test theoretical predictions for several properties of the echo formation such as the variation in momentum transfer due to the change in the angle between the traveling wave components of the excitation pulses, strength of the atom-field interaction, and the effect of spatial profile of the excitation beams. These studies are important for realizing precision measurements of the atomic fine structure constant and gravity using this interferometer.

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

    SciTech Connect

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

    2012-01-10

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

  16. Measurement of visible and UV emission from Energetic Neutral Atom Precipitation (ENAP), on Spacelab

    NASA Technical Reports Server (NTRS)

    Tinsley, B. A.

    1980-01-01

    The charge exchange of plasmaspheric ions and exospheric H and O and of solar wind ions with exospheric and interplanetary H are sources of precipitating neutrals whose faint emission may be observed by the imaging spectrometric observatory during dark periods of the SL-1 orbit. Measurements of the interactions of these precipitating atoms with the thermosphere are needed to evaluate the heating and ionization effects on the atmosphere as well as the selective loss of i energetic ions from the sources (predominantly the ring current).

  17. [Determination of trace niobium and tantalum in rock sample by atomic emission spectrometry].

    PubMed

    Li, Hui-zhi; Zhou, Chang-li; Luo, Chuan-nan

    2002-10-01

    This paper describes the determination of trace Nb and Ta in sample using carbon powder and hafnium oxide as buffer by atomic emission spectrometry (AES). Hafnium has been selected as internal standard, since it has scinilar evaporation curve as those of Nb and Ta. Samples can be analyzed without chemical pretreatment. The sample was directly loaded onto the ordinary electrode. The method is simple, rapid and accurate. The range of determination for Nb and Ta are 0%-0.25% and 0%-0.125% respectively, and the detection limits are found to be 0.003% and 0.001%, respectively. Satisfactory results are obtained.

  18. The extreme wings of atomic emission and absorption lines. [in low pressure gases

    NASA Technical Reports Server (NTRS)

    Dalgarno, A.; Sando, K. M.

    1973-01-01

    Consideration of the extreme wings of atomic and molecular emission and absorption lines in low pressure gases. Classical and semiclassical results are compared with accurate quantal calculations of the self-broadening of Lyman-alpha in the hydrogen absorption spectrum that arises from quasimolecular transition. The results of classical, quantal, and semiclassical calculations of the absorption coefficient in the red wing are shown for temperatures of 500, 200, and 100 K. The semiclassical and quantal spectra agree well in shape at 500 K. Various other findings are discused.

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

    NASA Astrophysics Data System (ADS)

    Raghuram, Susarla; Bhardwaj, Anil

    2014-06-01

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

  20. Problems, possibilities and limitations of inductively coupled plasma atomic emission spectrometry in the determination of platinum, palladium and rhodium in samples with different matrix composition

    NASA Astrophysics Data System (ADS)

    Petrova, P.; Velichkov, S.; Velitchkova, N.; Havezov, I.; Daskalova, N.

    2010-02-01

    The economic and geological importance of platinum group of elements has led to the development of analytical methods to quantify them in different types of samples. In the present paper the quantitative information for spectral interference in radial viewing 40.68 MHz inductively coupled plasma atomic emission spectrometry in the determination of Pt, Pd and Rh in the presence of complex matrix, containing Al, Ca, Fe, Mg, Mn, P and Ti as matrix constituents was obtained. The database was used for optimum line selections. By using the selected analysis lines the following detection limits in ng g - 1 were obtained: Pt 1700, Pd-1440, Rh-900. The reached detection limits determine the possibilities and limitation of the direct ICP-AES method in the determination of Pt, Pd and Rh in geological and environmental materials. The database for spectral interferences in the presence of aluminum can be used for the determination of platinum group of elements in car catalysts. The accuracy of the analytical results was experimentally demonstrated by two certified reference materials that were analyzed: SARM 7, Pt ore and recycled auto-catalyst certified reference material SRM 2556.

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

    NASA Technical Reports Server (NTRS)

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

    2007-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    2007-01-01

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

  3. Fluorescence emission of Ca-atom from photodissociated Ca2 in Ar-doped helium droplets. I. Experimental.

    PubMed

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

    2012-11-14

    The Ca(2) → Ca(4s4p(1)P) + Ca(4s(2)(1)S) photodissociation was investigated in a He droplet isolation experiment where the droplets are doped by Ar atoms. Fluorescence spectra associated with the Ca(4s4p(1)P → 4s(2)(1)S) emission were recorded as a function of the average number of Ar atoms per droplet. Three contributions were observed depending on whether the emitting Ca atoms are free, bound to helium atoms or bound to argon atoms. Moreover, the full Ca(4s4p(1)P → 4s(2)(1)S) fluorescence emission was recorded as a function of the wavelength of the photodissociation laser, hence providing the action spectrum of the Ca(2) → Ca(4s4p(1)P) + Ca(4s(2)(1)S) process. The latter spectrum suggests that in He droplets doped by argon, Ca atoms are attracted inside the droplet where they associate as Ca(2). Full analysis of the spectra indicate that the emission of Ca bound to a single Ar atom is redshifted by 94 cm(-1) with respect to the emission of free Ca.

  4. An Atomically Precise Au10 Ag2 Nanocluster with Red-Near-IR Dual Emission.

    PubMed

    Lei, Zhen; Guan, Zong-Jie; Pei, Xiao-Li; Yuan, Shang-Fu; Wan, Xian-Kai; Zhang, Jin-Yuan; Wang, Quan-Ming

    2016-08-01

    A red-near-IR dual-emissive nanocluster with the composition [Au10 Ag2 (2-py-C≡C)3 (dppy)6 ](BF4 )5 (1; 2-py-C≡C is 2-pyridylethynyl, dppy=2-pyridyldiphenylphosphine) has been synthesized. Single-crystal X-ray structural analysis reveals that 1 has a trigonal bipyramidal Au10 Ag2 core that contains a planar Au4 (2-py-C≡C)3 unit sandwiched by two Au3 Ag(dppy)3 motifs. Cluster 1 shows intense red-NIR dual emission in solution. The visible emission originates from metal-to-ligand charge transfer (MLCT) from silver atoms to phosphine ligands in the Au3 Ag(dppy)3 motifs, and the intense NIR emission is associated with the participation of 2-pyridylethynyl in the frontier orbitals of the cluster, which is confirmed by a time-dependent density functional theory (TD-DFT) calculation. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Novel method for the fast preconcentration and monitoring of a ppt level of lead and copper with a modified hexagonal mesoporous silica compound and inductively coupled plasma atomic emission spectrometry.

    PubMed

    Ganjali, Mohammad Reza; Babaei, Leila Hajiagha; Badiei, Alireza; Ziarani, Ghodsi Mohammadi; Tarlani, Aliakbar

    2004-04-01

    A novel method for the rapid extraction and determination of a ppt level of Pb2+ and Cu2+ ions using partial silylated MCM-41 modified by a new salophen and inductively coupled plasma atomic emission spectrometry (ICP-AES) is introduced. The preconcentration factor of the method is 500, and the detection limits of Pb2+ and Cu2+ are 335 and 34 ng L(-1), respectively. The time and efficiency of extraction, the pH and flow rate, the type and minimum amount of acid for stripping of Pb2+ and Cu2+ from modified MCM-41 and the break-through volume were investigated. The maximum capacity of 4 mg of silylated MCM-41 modified by salophen used was found to be 150 +/- 4 and 117 +/- 3 microg of Pb2+ and Cu2+, respectively.

  6. Field electron emission of layered Bi2Se3 nanosheets with atom-thick sharp edges

    NASA Astrophysics Data System (ADS)

    Huang, Huihui; Li, Yuan; Li, Qi; Li, Borui; Song, Zengcai; Huang, Wenxiao; Zhao, Chujun; Zhang, Han; Wen, Shuangchun; Carroll, David; Fang, Guojia

    2014-06-01

    Field electron emission properties of solution processed few-layer Bi2Se3 nanosheets are studied for the first time, which exhibit a low turn-on field of 2.3 V μm-1, a high field enhancement factor of up to 6860 and good field emission stability. This performance is better than that of the as reported layered MoS2f sheets and is comparable to that of single layer graphene films. The efficient field emission behaviours are found to be not only attributed to their lower work function but also related to their numerous sharp edges or protrusion decorated structure based on our simulation results. Besides, the contribution of possible two-dimensional electron gas surface states of atom-thick layered Bi2Se3 nanosheets is discussed in this paper. We anticipate that these solution processed layered Bi2Se3 nanosheets have great potential as robust high-performance vertical structure electron emitters for future light weight and highly flexible vacuum micro/nano-electronic device applications.Field electron emission properties of solution processed few-layer Bi2Se3 nanosheets are studied for the first time, which exhibit a low turn-on field of 2.3 V μm-1, a high field enhancement factor of up to 6860 and good field emission stability. This performance is better than that of the as reported layered MoS2f sheets and is comparable to that of single layer graphene films. The efficient field emission behaviours are found to be not only attributed to their lower work function but also related to their numerous sharp edges or protrusion decorated structure based on our simulation results. Besides, the contribution of possible two-dimensional electron gas surface states of atom-thick layered Bi2Se3 nanosheets is discussed in this paper. We anticipate that these solution processed layered Bi2Se3 nanosheets have great potential as robust high-performance vertical structure electron emitters for future light weight and highly flexible vacuum micro/nano-electronic device applications

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

    NASA Astrophysics Data System (ADS)

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

    2016-01-01

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

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

    NASA Astrophysics Data System (ADS)

    Mondal, Abhoy; Mandal, Chittranjan; Purkait, Malay

    2016-01-01

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

  9. Dynamic emission and population control in a Λ-type excitation scheme of atomic potassium

    NASA Astrophysics Data System (ADS)

    Papademetriou, G.; Pentaris, D.; Efthimiopoulos, T.; Lyras, A.

    2017-06-01

    The nonlinear interaction of a four-level atomic configuration in potassium, with ns pump and coupling fields, is numerically investigated. The resonant pump acts on the two-photon transition | 4{{{S}}}{1/2}> ≤ftrightarrow | 6{{{S}}}{1/2}> causing internally generated emissions in two atomic paths: path-1, | 4{{{S}}}{1/2}> ≤ftrightarrow | 6{{{S}}}{1/2}> ≤ftrightarrow | 5{{{P}}}{3/2}> ≤ftrightarrow | 4{{{S}}}{1/2}> , and path-2, | 4{{{S}}}{1/2}> ≤ftrightarrow | 6{{{S}}}{1/2}> ≤ftrightarrow | 4{{{P}}}{3/2}> ≤ftrightarrow | 4{{{S}}}{1/2}> , respectively. The coupling laser resonantly excites the single-photon transition | 6{{{S}}}{1/2}> \\to | 4{{{P}}}{3/2}> in a Λ-type scheme. A controlled temporal shift and enhancement of the partially coherent cascade emissions of path-2 is obtained. The amplification without inversion mechanism is proposed to explain the lower path-2 emission. It is shown that when the coupling field is delayed from the pump, then an efficient dynamic effect is induced, based on an additional population interplay of states | 6{{{S}}}{1/2}> and | 4{{{P}}}{3/2}> . Finally, a novel coherent method for temporally controlling the quasi-stationary population dynamics in a saturated system is proposed, when the driving fields are also delayed. The importance of the present work is related to the fact that the induced coherence (polarisation or energy injection) of the coupling field can be temporally controlled in nonlinear gaseous media.

  10. Hydrogen-like atom in a superstrong magnetic field: Photon emission and relativistic energy level shift

    NASA Astrophysics Data System (ADS)

    Skobelev, V. V.

    2017-06-01

    Following our previous work, additional arguments are presented that in superstrong magnetic fields B ≫ (Zα)2 B 0, B 0 = m 2 c 3/ eħ ≈ 4.41 × 1013 G, the Dirac equation and the Schrödinger equation for an electron in the nucleus field following from it become spatially one-dimensional with the only z coordinate along the magnetic field, "Dirac" spinors become two-component, while the 2 × 2 matrices operate in the {0; 3} subspace. Based on the obtained solution of the Dirac equation and the known solution of the "onedimensional" Schrödinger equation by ordinary QED methods extrapolated to the {0; 3} subspace, the probability of photon emission by a "one-dimensional" hydrogen-like atom is calculated, which, for example, for the Lyman-alpha line differs almost twice from the probability in the "three-dimensional" case. Similarly, despite the coincidence of nonrelativistic energy levels, the calculated relativistic corrections of the order of (Zα)4 substantially differ from corrections in the absence of a magnetic field. A conclusion is made that, by analyzing the hydrogen emission spectrum and emission spectra at all, we can judge in principle about the presence or absence of superstrong magnetic fields in the vicinity of magnetars (neutron stars and probably brown dwarfs). Possible prospects of applying the proposed method for calculations of multielectron atoms are pointed out and the possibility of a more reliable determination of the presence of superstrong magnetic fields in magnetars by this method is considered.

  11. Numerical modelling of emission of a two-level atom near a metal nanoparticle with account for tunnelling of an electron from an atom into a particle

    SciTech Connect

    Fedorovich, S V; Protsenko, I E

    2016-01-31

    We report the results of numerical modelling of emission of a two-level atom near a metal nanoparticle under resonant interaction of light with plasmon modes of the particle. Calculations have been performed for different polarisations of light by a dipole approximation method and a complex multipole method. Depending on the distance between a particle and an atom, the contribution of the nonradiative process of electron tunnelling from a two-level atom into a particle, which is calculated using the quasi-classical approximation, has been taken into account and assessed. We have studied spherical gold and silver particles of different diameters (10 – 100 nm). The rates of electron tunnelling and of spontaneous decay of the excited atomic state are found. The results can be used to develop nanoscale plasmonic emitters, lasers and photodetectors. (nanooptics)

  12. Element analysis and characteristic identification of non-fumigated and sulfur-fumigated Fritillaria thunbergii Miq. using microwave digestion-inductively coupled plasma atomic emission spectrometry combined with Fourier transform infrared spectrometry

    PubMed Central

    Lou, Yajing; Cai, Hao; Liu, Xiao; Tu, Sicong; Pei, Ke; Zhao, Yingying; Cao, Gang; Li, Songlin; Qin, Kunming; Cai, Baochang

    2014-01-01

    Background: Sulfur-fumigation may induce chemical transformation of traditional Chinese medicines leading to harmful effects following patient ingestion. For quality control, it is urgently needed to develop a reliable and efficient method for sulfur-fumigation identification. Materials and Methods: The spectrochemical identification of non-fumigated and sulfur-fumigated Fritillaria thunbergii Miq. was carried out to evaluate inorganic elements and organic components. The concentrations of 12 elements, including Zn, Mn, Cu, Fe, Li, Mg, Sr, Pb, As, Cd, Hg, and S of samples were determined by microwave digestion - inductively coupled plasma atomic emission spectrometry (ICP-AES). Meanwhile, Fourier transform infrared spectrometry (FTIR) was used for the study of chemical group characteristic reactions after sulfur-fumigation. Results: The concentrations of Fe, Mg, Hg, and S elements showed significant differences between non-fumigated and sulfur-fumigated Fritillaria thunbergii Miq. The characteristic stretching vibrations of some groups in FTIR spectra, such as -OH, -S = O and -S-O, provided the identification basis for the discrimination of non-fumigated and sulfur-fumigated Fritillaria thunbergii Miq. Conclusion: The application of microwave digestion - ICP-AES was successfully used in combination with FTIR to authenticate and evaluate the quality of medicinal Fritillaria thunbergii Miq. Further applications of this technique should be explored. PMID:24914306

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

    PubMed

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

    2016-04-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-01-01

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

  15. Measurement of Trace Metals in Tobacco and Cigarette Ash by Inductively Coupled Plasma-Atomic Emission Spectroscopy

    NASA Astrophysics Data System (ADS)

    Wang, W.; Finlayson-Pitts, B. J.

    2003-01-01

    The ICP AES experiment reported here is suitable for use in a junior- or senior-level undergraduate instrumental analysis laboratory. The objective of this experiment is to analyze trace metals present in cigarette tobacco, the cigarette filter, and the ash obtained when the cigarette is burned. Two different brands of cigarettes, one with and one without a filter, were used. The filter was analyzed before and after smoke was drawn through it. The trace metals were extracted using concentrated nitric acid at room temperature and at 100 °C respectively, to test the extraction efficiency. Some tobacco samples were spiked with ZnCl2 and FeCl3 to assess the efficiency of the recovery. Zinc and iron are shown to be present in tobacco, filter, and ash, while chromium was above the detection limit only in the ash. These metals are concentrated in the ash compared to the tobacco by factors of ˜4 (Zn), 12 17 (Fe), and ≥ 2 (Cr). If sufficient laboratory time is available, this experiment could be paired with one using atomic absorption (AA) to demonstrate the advantages and disadvantages of ICP when compared to AA.

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

    NASA Technical Reports Server (NTRS)

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

    1975-01-01

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

  17. Evaluation of several pneumatic micronebulizers with different designs for use in ICP-AES and ICP-MS. Future directions for further improvement.

    PubMed

    Maestre, S E; Todolí, J L; Mermet, J M

    2004-07-01

    This paper reports characterization of the behavior of five pneumatic micronebulizers based on slightly different designs in inductively coupled plasma atomic-emission spectrometry and mass spectrometry (ICP-AES and ICP-MS). Two nebulizers were used as reference nebulizers, a high-efficiency nebulizer (HEN) and a micromist (MM). They were compared with a commercially available PFA (tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer) nebulizer and with two new prototypes called the polymeric pneumatic concentric nebulizer (PMN) and the high-solids micronebulizer (HSM). The dimensions of the nebulizers, the gas back-pressure, and the free liquid uptake rates were measured. The study also included tertiary aerosol drop-size distributions, analyte transport rate, and analytical figures of merit, i.e. sensitivities and limits of detection, both in ICP-AES and ICP-MS. Recoveries for two food solid reference materials were also determined. Overall, the results indicated that the PFA and the HEN nebulizers provided the best results. These two nebulizers delivered a higher mass of analyte to the plasma and showed better sensitivies giving lower limits of detection than the PMN, HSM and MM. The results revealed that the liquid prefilming effect occurring before aerosol production in the PFA nebulizer promoted more efficient interaction of liquid and gas, thus affording good results even though gas back-pressure values could be maintained below 3 bar. In contrast, the HEN had to be operated at about 7 bar under the same conditions. Nebulizer design did not have a relevant effect on the recovery, which confirmed that the spray chamber plays an important role in terms of non-spectroscopic interferences.

  18. Study of uranium matrix interference on ten analytes using inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Ghazi, A. A.; Qamar, Sajid; Atta, M. A.

    1993-08-01

    Maximum allowable concentrations of 12 elements in uranium hexafluoride feed for enrichment to reactor grade material (about 3%), vary from 1 to 100 ppm ( μg/g). Using an inductively coupled plasma atomic emission spectrometer, 51 lines of ten of these elements (B, Cr, Mo, P, Sb, Si, Ta, Ti, V and W) have been studied with a uranium matrix to investigate the matrix interference on the basis of signal to background (SBR), and background to background ratios (BBR). Detection limits and limits of quantitative determination (LQDs) were calculated for these elements in a uranium matrix using SBR and relative standard deviation of the background signal (RSD B) approach. In almost all cases, the uranium matrix interference reduces the SBRs to the extent that direct trace analysis is impossible. A uranium sample having known concentrations of impurities (around LQDs) was directly analysed with results that showed reasonable accuracy and precision.

  19. Gravitational properties of light: The emission of counter-propagating laser pulses from an atom

    NASA Astrophysics Data System (ADS)

    Rätzel, Dennis; Wilkens, Martin; Menzel, Ralf

    2017-04-01

    The gravitational field of a laser pulse, although not detectable at the moment, has a special feature which continues to attract attention; cause and effect propagate with the same speed, the speed of light. One particular result of this feature is that the gravitational field of an emitted laser pulse and the gravitational effect of the emitter's energy-momentum change are intimately entangled. In this article, a specific example of an emission process is considered: An atom, modeled as a point mass, emits two counter-propagating pulses. The corresponding curvature and the effect on massive and massless test particles is discussed. A comparison is made with the metric corresponding to a spherically symmetric massive object that isotropically emits radiation; the Vaidya metric.

  20. Near-threshold emission of electrons during grazing scattering of keV Ne atoms from an Al(111) surface

    SciTech Connect

    Matulevich, Y.; Lederer, S.; Winter, H.

    2005-01-15

    The number of electrons emitted during grazing scattering of Ne atoms with kilo-electron-volt energies from an Al(111) surface is recorded in coincidence with the energy loss of scattered projectiles. Irrespective of the total projectile energies used, we observe a pronounced increase of total electron emission yields when the energy for motion normal to the surface exceeds about 25 eV. Based on energy loss spectra and classical computer simulations of projectile trajectories we attribute electron emission under these scattering conditions to a promotion mechanism in binary collisions between Ne and Al target atoms resulting in single and double excitations of projectiles.

  1. Thermal Processes and Emission of Atoms from the Liquid Phase Target Surface of a Magnetron Sputtering System

    NASA Astrophysics Data System (ADS)

    Bleykher, G. A.; Krivobokov, V. P.; Yuryeva, A. V.

    2015-08-01

    Mathematical models of thermal and erosion processes in the thermally insulated target of a magnetron sputtering system are constructed. With their help, the special features of forming the emission flux of atoms from the surface of the target whose material experiences first order phase transformations are obtained. The influence of the power density deposited into the magnetron discharge is investigated, the inhomogeneity of its distribution over the target surface is considered, and the special features of atom emission in pulsed-periodic plasma generation regimes are studied. The efficiency of the models is confirmed by a comparison of the calculated results with experimental measurements.

  2. Investigations on laser ablation microwave induced plasma atomic emission spectrometry using polymer samples

    NASA Astrophysics Data System (ADS)

    Leis, F.; Bauer, H. E.; Prodan, L.; Niemax, K.

    2001-01-01

    The potential of laser ablation-microwave induced plasma-atomic emission spectrometry (LA-MIP-AES) for the analysis of plastic materials has been investigated. A Nd/YAG laser, operated in its fundamental mode at 1064 nm, was used to ablate small amounts of various plastics. The sample atoms were transported and excited in a closely neighbored continuously running microwave induced plasma (MIP) operated in argon or helium at reduced pressure. A 0.5-m échelle spectrometer, equipped with an intensified charge coupled device (ICCD) as a detector was used for recording the spectra. The amount of ablated material was found to be strongly dependent on the matrix (10-190 ng/shot). Signals for some metals often used as additives in polymers (Al, Ca, Cu, Sb, Ti) and for the elements F, Cl, Br, J, and P in various polymers were recorded in the spectral range 250-840 nm. The estimated detection limits were found to be in the range 0.001-0.08% for metals and 0.05-0.7% for non-metals. Spectral lines of fluorine and iodine could only be measured in the helium MIP. For high concentrations of chlorine and carbon in the samples (polyvinylchloride), a memory effect was observed.

  3. [Application of atomic emission spectroscopy analysis in the atmospheric pressure plasma polishing process study].

    PubMed

    Wang, Bo; Zhang, Ju-Fan; Dong, Shen

    2008-07-01

    The atmospheric pressure plasma polishing (APPP) is a novel precision machining technology. It performs the atom scale material removal based on low temperature plasma chemical reactions. As the machining process is chemical in nature, it avoids the surface/subsurface defects usually formed in conventional mechanical machining processes. APPP firstly introduces a capacitance coupled radio frequency (RF) plasma torch to generate reactive plasma and excite chemical reactions further. The removal process is a complicated integrating action which tends to be affected by many factors, such as the gas ratio, the RF power and so on. Therefore, to improve the machining quality, all the aspects should be considered and studied, to establish the foundation for further model building and theoretical analysis. The atomic emission spectroscopy analysis was used to study the process characteristics. A commercial micro spectrometer was used to collect the spectrograms under different parameters, by comparing which the influence of the RF power and gas ratio was initially studied. The analysis results indicate that an increase in RF power results in a higher removal rate within a certain range. The gas ratio doesn't show obvious influence on the removal rate and surface roughness in initial experiments, but the element compositions detected by X-ray photoelectron spectroscopy technology on the machined surfaces under different ratios really indicate distinct difference. Then the theoretical analysis revealed the corresponding electron transition orbits of the excited reactive fluorine atoms, which is necessary for further mechanism research and apparatus improvement. Then the initial process optimization was made based on the analysis results, by which the Ra 0.6 nm surface roughness and 32 mm3 x min(-1) removal rate were achieved on silicon wafers.

  4. A table of polyatomic interferences in ICP-MS

    USGS Publications Warehouse

    May, Thomas W.; Wiedmeyer, Ray H.

    1998-01-01

    Spectroscopic interferences are probably the largest class of interferences in ICP-MS and are caused by atomic or molecular ions that have the same mass-to-charge as analytes of interest. Current ICP-MS instrumental software corrects for all known atomic “isobaric” interferences, or those caused by overlapping isotopes of different elements, but does not correct for most polyatomic interferences. Such interferences are caused by polyatomic ions that are formed from precursors having numerous sources, such as the sample matrix, reagents used for preparation, plasma gases, and entrained atmospheric gases.

  5. Quantification of immobilized Candida antarctica lipase B (CALB) using ICP-AES combined with Bradford method.

    PubMed

    Nicolás, Paula; Lassalle, Verónica L; Ferreira, María L

    2017-02-01

    The aim of this manuscript was to study the application of a new method of protein quantification in Candida antarctica lipase B commercial solutions. Error sources associated to the traditional Bradford technique were demonstrated. Eight biocatalysts based on C. antarctica lipase B (CALB) immobilized onto magnetite nanoparticles were used. Magnetite nanoparticles were coated with chitosan (CHIT) and modified with glutaraldehyde (GLUT) and aminopropyltriethoxysilane (APTS). Later, CALB was adsorbed on the modified support. The proposed novel protein quantification method included the determination of sulfur (from protein in CALB solution) by means of Atomic Emission by Inductive Coupling Plasma (AE-ICP). Four different protocols were applied combining AE-ICP and classical Bradford assays, besides Carbon, Hydrogen and Nitrogen (CHN) analysis. The calculated error in protein content using the "classic" Bradford method with bovine serum albumin as standard ranged from 400 to 1200% when protein in CALB solution was quantified. These errors were calculated considering as "true protein content values" the results of the amount of immobilized protein obtained with the improved method. The optimum quantification procedure involved the combination of Bradford method, ICP and CHN analysis. Copyright © 2016 Elsevier Inc. All rights reserved.

  6. ICP-AES determination of minor- and major elements in apples after microwave assisted digestion.

    PubMed

    Juranović Cindrić, Iva; Krizman, Ivona; Zeiner, Michaela; Kampić, Štefica; Medunić, Gordana; Stingeder, Gerhard

    2012-12-15

    The aim of this paper was to determine the content of minor and major elements in apples by inductively coupled plasma atomic emission spectrometry (ICP-AES). Prior to ICP-AES measurement, dried apples were digested in a microwave assisted digestion system. The differences in the measured element concentrations after application of open and closed microwave system as sample preparation procedures are discussed. In whole apples, flesh and peel Ag, Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, Sr and Zn were analysed after optimisation and validating the analytical method using ICP-AES. The accuracy of the method determined by spiking experiments was very good (recoveries 88-115%) and the limits of detection of elements of interest were from 0.01 up to 14.7 μg g(-1). The reference ranges determined in all apple samples are 39-47 mg g(-1) for K, 9-14 mg g(-1) for Na, 3-7 mg g(-1) for Mg, 3-7 μg g(-1) for Zn, 0.7-2.8 μg g(-1) for Sr. The range of Mn in peel 4-6 μg g(-1) is higher compared to whole apple from 0.7 to 1.7 μg g(-1). Cd is found only in peel, in the concentration range of 0.4-1.1 μg g(-1).

  7. Determination of aluminium in groundwater samples by GF-AAS, ICP-AES, ICP-MS and modelling of inorganic aluminium complexes.

    PubMed

    Frankowski, Marcin; Zioła-Frankowska, Anetta; Kurzyca, Iwona; Novotný, Karel; Vaculovič, Tomas; Kanický, Viktor; Siepak, Marcin; Siepak, Jerzy

    2011-11-01

    The paper presents the results of aluminium determinations in ground water samples of the Miocene aquifer from the area of the city of Poznań (Poland). The determined aluminium content amounted from <0.0001 to 752.7 μg L(-1). The aluminium determinations were performed using three analytical techniques: graphite furnace atomic absorption spectrometry (GF-AAS), inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS). The results of aluminium determinations in groundwater samples for particular analytical techniques were compared. The results were used to identify the ascent of ground water from the Mesozoic aquifer to the Miocene aquifer in the area of the fault graben. Using the Mineql+ program, the modelling of the occurrence of aluminium and the following aluminium complexes: hydroxy, with fluorides and sulphates was performed. The paper presents the results of aluminium determinations in ground water using different analytical techniques as well as the chemical modelling in the Mineql+ program, which was performed for the first time and which enabled the identification of aluminium complexes in the investigated samples. The study confirms the occurrence of aluminium hydroxy complexes and aluminium fluoride complexes in the analysed groundwater samples. Despite the dominance of sulphates and organic matter in the sample, major participation of the complexes with these ligands was not stated based on the modelling.

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

    NASA Astrophysics Data System (ADS)

    Sandhya, S. N.

    2007-01-01

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

  9. Direct solid analysis of powdered tungsten carbide hardmetal precursors by laser-induced argon spark ablation with inductively coupled plasma atomic emission spectrometry.

    PubMed

    Holá, Markéta; Kanický, Viktor; Mermet, Jean-Michel; Otruba, Vítezslav

    2003-12-01

    The potential of the laser-induced argon spark atomizer (LINA-Spark atomizer) coupled with ICP-AES as a convenient device for direct analysis of WC/Co powdered precursors of sintered hardmetals was studied. The samples were presented for the ablation as pressed pellets prepared by mixing with powdered silver binder containing GeO2 as internal standard. The pellets were ablated with the aid of a Q-switched Nd:YAG laser (1064 nm) focused 16 mm behind the target surface with a resulting estimated power density of 5 GW cm(-2). Laser ablation ICP-AES signals were studied as a function of ablation time, and the duration of time prior to measurement (pre-ablation time) which was necessary to obtain reliable results was about 40 s. Linear calibration plots were obtained up to 10% (m/m) Ti, 9% Ta and 3.5% Nb both without internal standardization and by using germanium as an added internal standard or tungsten as a contained internal standard. The relative uncertainty at the centroid of the calibration line was in the range from +/- 6% to +/- 11% for Nb, Ta and Ti both with and without internal standardisation by Ge. A higher spread of points about the regression was observed for cobalt for which the relative uncertainty at the centroid was in the range from +/- 9% to +/- 14%. Repeatability of results was improved by the use of both Ge and W internal standards. The lowest determinable quantities calculated for calibration plots were 0.060% Co, 0.010% Nb, 0.16% Ta and 0.030% Ti with internal standardization by Ge. The LA-ICP-AES analyses of real samples led to good agreement with the results obtained by solution-based ICP determination with a relative bias not exceeding 10%. The elimination of the dissolution procedure of powdered tungsten (Nb, Ta, Ti) carbide is the principal advantage of the developed LA-ICP-AES method.

  10. Determination of trace elements in uranium by inductively coupled plasma-atomic emission spectrometry using Kalman filtering

    SciTech Connect

    Veen, E.H. van; de Loos-Vollebregt, T.C. de; Wassink, A.P.; Kalter, H.

    1992-08-01

    Trace impurities in uranium hexafluoride were analyzed by ICP-AES. The data were reduced using a Kalman filtering technique. Normally, multiple extraction steps are required for this analysis using conventional ICP-AES.

  11. Electron emission perpendicular to the polarization direction in laser-assisted XUV atomic ionization

    NASA Astrophysics Data System (ADS)

    Gramajo, A. A.; Della Picca, R.; Arbó, D. G.

    2017-08-01

    We present a theoretical study of ionization of the hydrogen atom due to an XUV pulse in the presence of an infrared (IR) laser with both fields linearly polarized in the same direction. In particular, we study the energy distribution of photoelectrons emitted perpendicularly to the polarization direction. As we previously showed in Gramajo et al. [Phys. Rev. A 94, 053404 (2016), 10.1103/PhysRevA.94.053404] for parallel emission, by means of a very simple semiclassical model which considers electron trajectories born at different ionization times, the electron energy spectrum can be interpreted as the interplay of intra- and intercycle interferences. However, contrary to the case of parallel emission the intracycle interference pattern stems from the coherent superposition of four electron trajectories giving rise to (i) interference of electron trajectories born during the same half cycle (intra-half-cycle interference) and (ii) interference between electron trajectories born during the first half cycle with those born during the second half cycle (inter-half-cycle interference). The intercycle interference is responsible for the formation of the sidebands. We also show that the destructive inter-half-cycle interference for the absorption and emission of an even number of IR laser photons is responsible for the characteristic sidebands in the perpendicular direction separated by twice the IR photon energy. This contrasts with the emission along the polarization axis (all sideband orders are present) since intra-half-cycle interferences do not exist in that case. The intracycle interference pattern works as a modulation of the sidebands and, in the same way, it is modulated by the intra-half-cycle interference pattern. We analyze the dependence of the energy spectrum on the laser intensity and the time delay between the XUV pulse and the IR laser. Finally, we show that our semiclassical simulations are in very good agreement with quantum calculations within the

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

    PubMed

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

    2012-11-14

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

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

    ERIC Educational Resources Information Center

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

    2016-01-01

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

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

    EPA Science Inventory

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

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

    EPA Science Inventory

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

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

    EPA Science Inventory

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

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

    ERIC Educational Resources Information Center

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

    2016-01-01

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

  18. Analytical performance of an r.f. capacitively coupled plasma for atomic emission with tip-ring electrode geometry.

    PubMed

    Frenţiu, T; Rusu, A M; Ponta, M; Anghel, S D; Cordos, E A

    1996-06-01

    A low to medium power radiofrequency capacitively coupled plasma is characterized as spectral source for atomic emission. The signal to background ratio and the limits of detection were determined for 19 elements as a function of the plasma torch geometry and the observation point.

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

    EPA Science Inventory

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

  20. Environmental Indicators of Metal Pollution and Emission: An Experiment for the Instrumental Analysis Laboratory

    ERIC Educational Resources Information Center

    Bowden, John A.; Nocito, Brian A.; Lowers, Russell H.; Guillette, Louis J., Jr.; Williams, Kathryn R.; Young, Vaneica Y.

    2012-01-01

    This experiment enlightens students on the use of environmental indicators and inductively coupled plasma-atomic emission spectroscopy (ICP-AES) and demonstrates the ability of these monitoring tools to measure metal deposition in environmental samples (both as a result of lab-simulated and real events). In this two-part study, the initial…

  1. Environmental Indicators of Metal Pollution and Emission: An Experiment for the Instrumental Analysis Laboratory

    ERIC Educational Resources Information Center

    Bowden, John A.; Nocito, Brian A.; Lowers, Russell H.; Guillette, Louis J., Jr.; Williams, Kathryn R.; Young, Vaneica Y.

    2012-01-01

    This experiment enlightens students on the use of environmental indicators and inductively coupled plasma-atomic emission spectroscopy (ICP-AES) and demonstrates the ability of these monitoring tools to measure metal deposition in environmental samples (both as a result of lab-simulated and real events). In this two-part study, the initial…

  2. Lead isotope ratios in lichen samples evaluated by ICP-ToF-MS to assess possible atmospheric pollution sources in Havana, Cuba.

    PubMed

    Alvarez, Alfredo Montero; Estévez Alvarez, Juan R; do Nascimento, Clístenes Williams Araújo; González, Iván Pupo; Rizo, Oscar Díaz; Carzola, Lázaro Lima; Torres, Roberto Ayllón; Pascual, Jorge Gómez

    2017-01-01

    Epiphytic lichens, collected from 119 sampling sites grown over "Roistonea Royal Palm" trees, were used to assess the spatial distribution pattern of lead (Pb) and identify possible pollution sources in Havana (Cuba). Lead concentrations in lichens and topsoils were determined by flame atomic absorption spectrophotometry and inductively coupled plasma (ICP) atomic emission spectrometry, respectively, while Pb in crude oils and gasoline samples were measured by ICP-time of flight mass spectrometry (ICP-ToF-MS). Lead isotopic ratios measurements for lichens, soils, and crude oils were obtained by ICP-ToF-MS. We found that enrichment factors (EF) reflected a moderate contamination for 71% of the samples (EF > 10). The (206)Pb/(207)Pb ratio values for lichens ranged from 1.17 to 1.20 and were a mixture of natural radiogenic and industrial activities (e.g., crude oils and fire plants). The low concentration of Pb found in gasoline (<7.0 μg L(-1)) confirms the official statement that leaded gasoline is no longer used in Cuba.

  3. ICPS Removal from Shipping Container

    NASA Image and Video Library

    2017-03-09

    Inside the United Launch Alliance (ULA) Horizontal Integration Facility at Cape Canaveral Air Force Station in Florida, a crane lifts the shipping container cover away from the Interim Cryogenic Propulsion Stage (ICPS) for NASA's Space Launch System rocket, followed by the ICPS bring removed and placed on a work stand for processing. The ICPS is the first integrated piece of flight hardware to arrive for the SLS. The ICPS arrived from the ULA facility in Decatur, Alabama. The ICPS is the in-space stage that is located toward the top of the rocket, between the Launch Vehicle Stage Adapter and the Orion Spacecraft Adapter. It will provide some of the in-space propulsion during Orion's first flight test atop the SLS on Exploration Mission 1.

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

    SciTech Connect

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

    1997-04-01

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

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

    NASA Astrophysics Data System (ADS)

    Slanger, T. G.

    2005-12-01

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

  6. The influence of atomic collisions on collective spontaneous emission from an f-deformed Bose-Einstein condensate

    NASA Astrophysics Data System (ADS)

    Haghshenasfard, Z.; Naderi, M. H.; Soltanolkotabi, M.

    2009-03-01

    In this paper, we investigate the spontaneous emission of an f-deformed Bose-Einstein condensate of a gas with N identical two-level atoms immersed in a single-mode ideal cavity with s atoms initially excited. We apply an f-deformed quantum model in which Gardiner's phonon operators are deformed by an operator-valued functionf(\\hat n) of the particle number operator \\hat n. We consider the collisions between the atoms as a special kind of f-deformation where the collision rate κ is regarded as a corresponding deformation parameter. The time evolution of the expectation value of the atomic inversion is presented, the phenomenon of collective collapses and revivals is shown and the effects of deformation on the cooperative behaviour of the system are discussed.

  7. Low flow, externally air cooled torch for inductively coupled plasma atomic emission spectrometry with axial viewing

    NASA Astrophysics Data System (ADS)

    Hasan, Towhid; Praphairaksit, Narong; Houk, R. S.

    2001-04-01

    The torch wall is cooled largely by air passing through a cooling jacket added to the outside of a Fassel torch. The plasma is viewed axially through a cooled cone interface centered on the axial channel. The outer argon gas flow can be reduced to 7 l min -1 with no compromise in performance or torch lifetime. The plasma exhibits the same 'robustness index' and interference effects from Na as the conventional, high-flow ICP supplied with the particular spectrometer used. Detection limits (DL) for lines at ˜200 nm are poorer by approximately a factor of two, while those for lines at ˜400 nm are actually better than values typically seen for the same lines by axial viewing of a conventional, high-flow ICP.

  8. Micro- and nano-volume samples by electrothermal, near-torch vaporization sample introduction using removable, interchangeable and portable rhenium coiled-filament assemblies and axially-viewed inductively coupled plasma-atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Badiei, Hamid R.; Lai, Bryant; Karanassios, Vassili

    2012-11-01

    An electrothermal, near-torch vaporization (NTV) sample introduction for micro- or nano-volume samples is described. Samples were pipetted onto coiled-filament assemblies that were purposely developed to be removable and interchangeable and were dried and vaporized into a small-volume vaporization chamber that clips onto any ICP torch with a ball joint. Interchangeable assemblies were also constructed to be small-size (e.g., less than 3 cm long with max diameter of 0.65 cm) and light-weight (1.4 g) so that they can be portable. Interchangeable assemblies with volume-capacities in three ranges (i.e., < 1 μL, 1-10 μL and 10-100 μL) were fabricated and used. The horizontally-operated NTV sample introduction was interfaced to an axially-viewed ICP-AES (inductively coupled plasma-atomic emission spectrometry) system and NTV was optimized using ICP-AES and 8 elements (Pb, Cd, Zn, V, Ba, Mg, Be and Ca). Precision was 1.0-2.3% (peak height) and 1.1-2.4% (peak area). Detection limits (obtained using 5 μL volumes) expressed in absolute-amounts ranged between 4 pg for Pb to 0.3 fg (~ 5 million atoms) for Ca. Detection limits expressed in concentration units (obtained using 100 μL volumes of diluted, single-element standard solutions) were: 50 pg/mL for Pb; 10 pg/mL for Cd; 9 pg/mL for Zn; 1 pg/mL for V; 0.9 pg/mL for Ba; 0.5 pg/mL for Mg; 50 fg/mL for Be; and 3 fg/mL for Ca. Analytical capability and utility was demonstrated using the determination of Pb in pg/mL levels of diluted natural water Certified Reference Material (CRM) and the determination of Zn in 80 nL volumes of the liquid extracted from an individual vesicle. It is shown that portable and interchangeable assemblies with dried sample residues on them can be transported without analyte loss (for the concentrations tested), thus opening up the possibility for "taking part of the lab to the sample" applications, such as testing for Cu concentration-compliance with the lead-copper rule of the Environmental

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

    SciTech Connect

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

    2014-04-28

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

  10. Intra- and intercycle interference of electron emissions in laser-assisted XUV atomic ionization

    NASA Astrophysics Data System (ADS)

    Gramajo, A. A.; Della Picca, R.; Garibotti, C. R.; Arbó, D. G.

    2016-11-01

    We study the ionization of atomic hydrogen in the direction of polarization due to a linearly polarized XUV pulse in the presence of a strong IR laser. We describe the photoelectron spectra as an interference problem in the time domain. Electron trajectories stemming from different optical laser cycles give rise to intercycle interference energy peaks known as sidebands. These sidebands are modulated by a coarse-grained structure coming from the intracycle interference of the two electron trajectories born during the same optical cycle. We make use of a simple semiclassical model that offers the possibility to establish a connection between emission times and the photoelectron kinetic energy. We analyze such interference pattern as a function of the time delay between the IR and the XUV pulses and also as a function of the laser intensity. We compare the semiclassical predictions with the continuum-distorted-wave strong-field approximation and the ab initio solution of the time-dependent Schrödinger equation.

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

    PubMed

    Ozbek, Nil; Akman, Suleyman

    2016-02-01

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

  12. Analysis and Speciation of Lanthanoides by ICP-MS

    NASA Astrophysics Data System (ADS)

    Telgmann, Lena; Lindner, Uwe; Lingott, Jana; Jakubowski, Norbert

    2016-11-01

    Inductively coupled plasma mass spectrometry (ICP-MS) is based on formation of positively charged atomic ions in a high-frequency inductively coupled Argon plasma at atmospheric pressure. The ions are extracted and transferred from the plasma source into a mass analyzer operated at high vacuum via an interface equipped with a sampling and a skimmer cone. The ions are separated in the mass analyzer according to their charge to mass ratio. The ions are converted at a conversion dynode and are detected by use of a secondary electron multiplier or a Faraday cup. From an analytical point of view, ICP-MS is a well-established method for multi-elemental analysis in particular for elements at trace- and ultra-trace levels. Furthermore, methods based on ICP-MS offer simple quantification concepts, for which usually (liquid) standards are applied, low matrix effects compared to other conventional analytical techniques, and relative limits of detection (LODs) in the low pg g-1 range and absolute LODs down to the attomol range. For these applications, ICP-MS excels by a high sensitivity which is independent of the molecular structure and a wide linear dynamic range. It has found acceptance in various application areas and during the last decade ICP-MS is also more and more applied for detection of rare earth elements particularly in the life sciences. Due to the fact that all molecules introduced into the high temperature of the plasma in the ion source were completely dissociated and broken down into atoms, which are subsequently ionized, all elemental species information is completely lost. However, if the different species are separated before they enter the plasma by using adequate fractionation or separation techniques, then ICP-MS can be used as a very sensitive element-specific detector. We will discuss this feature of ICP-MS in this chapter in more detail at hand of the speciation of gadolinium-containing contrast agents.

  13. Crystallization-induced emission enhancement: A novel fluorescent Au-Ag bimetallic nanocluster with precise atomic structure

    PubMed Central

    Chen, Tao; Yang, Sha; Chai, Jinsong; Song, Yongbo; Fan, Jiqiang; Rao, Bo; Sheng, Hongting; Yu, Haizhu; Zhu, Manzhou

    2017-01-01

    We report the first noble metal nanocluster with a formula of Au4Ag13(DPPM)3(SR)9 exhibiting crystallization-induced emission enhancement (CIEE), where DPPM denotes bis(diphenylphosphino)methane and HSR denotes 2,5-dimethylbenzenethiol. The precise atomic structure is determined by x-ray crystallography. The crystalline state of Au4Ag13 shows strong luminescence at 695 nm, in striking contrast to the weak emission of the amorphous state and hardly any emission in solution phase. The structural analysis and the density functional theory calculations imply that the compact C–H⋯π interactions significantly restrict the intramolecular rotations and vibrations and thus considerably enhance the radiative transitions in the crystalline state. Because the noncovalent interactions can be easily modulated via varying the chemical environments, the CIEE phenomenon might represent a general strategy to amplify the fluorescence from weakly (or even non-) emissive nanoclusters. PMID:28835926

  14. Angular dependence of Doppler profiles of atomic emission produced in electron-molecule collisions: Estimation of anisotropy parameters

    NASA Astrophysics Data System (ADS)

    Nakashima, Keiji; Ogawa, Teiichiro

    1985-11-01

    The angular dependence of Doppler profiles of atomic fluorescence produced in electron impact dissociation of molecules was simulated in consideration of the effect of the anisotropy of dissociation and the ``polarization'' in magnetic sublevel. The asymmetry parameter b and the polarization of the electric vector of emission Jp are key parameters of Doppler profiles for the excited atom of known translational energy distribution. The difference of two Doppler profiles taken at 90° and 45°, which is denoted as angular difference Doppler profile, is shown to be useful to estimate these two key parameters.

  15. Simultaneous detection of selenium by atomic fluorescence and sulfur by molecular emission by flow-injection hydride generation with on-line reduction for the determination of selenate, sulfate and sulfite.

    PubMed

    Tyson, J F; Palmer, C D

    2009-10-12

    An inductively coupled plasma atomic fluorescence spectrometry (ICP-AFS) instrument, was modified so that it was capable of monitoring transient chromatographic or flow-injection profiles and that sulfur molecular emission and selenium atomic fluorescence could be monitored simultaneously in an argon-hydrogen diffusion flame on a glass burner. The analytes were introduced as hydrogen selenide and hydrogen sulfide, generated on a flow-injection manifold. Selenate was reduced to hydride-forming selenite by microwave-assisted on-line reaction with hydrochloric acid, and sulfate, or sulfite, was reduced to hydride-forming sulfide by a mixture of hydriodic acid, acetic acid and sodium hypophosphite. The effects of the nature of reducing agent, flow rate, microwave power and coil length were studied. The limit of detection (3s) for selenium was 10microgL(-1), and for sulfide was 70microgL(-1) (200-microL injection volume). The calibration was linear for selenium up to 2mgL(-1) and to 10mgL(-1) for sulfide. The throughput was 180h(-1). The three sulfur species could be differentiated on the basis of reactivity at various microwave powers.

  16. Excitation of O(1D) atoms in aurorae and emission of the forbidden OI 6300-A line

    NASA Technical Reports Server (NTRS)

    Rees, M. H.; Roble, R. G.

    1986-01-01

    The electron aurora leads to six processes capable of exciting the O(1D2) metastable state of the atomic-oxygen ground-state configuration, the parent state of the 6300-A red line. Altitude profiles of the volume emission rate resulting from each process are computed for Maxwellian electron spectra with characteristic energies between 0.1 and 2.0 keV. Since each process peaks at a different altitude, the sum or total volume emission rate extends over a wide altitude range. Measurements of 6300-A emission obtained by rocket and satellite-borne instruments are summarized, and it is shown that the chemical reaction of N(2D) with O2 is the major source of O(1D) atoms in the electron aurora. New calculations of the 6300-A:4728-A column emission-rate ratio are presented for a range of characteristic energies in an assumed Maxwellian electron spectrum. An approximate equation for the red-line emission per unit energy input is given as a function of electron-spectrum characteristic energy.

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

    NASA Astrophysics Data System (ADS)

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

    2016-10-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

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

  19. [Determination of high concentrations of rubidium chloride by ICP-OES].

    PubMed

    Zhong, Yuan; Sun, Bai; Li, Hai-jun; Wang, Tao; Li, Wu; Song, Peng-sheng

    2015-01-01

    The method of ICP-OES for the direct determination of high content of rubidium in rubidium chloride solutions was studied through mass dilution method and optimizing parameters of the instrument in the present paper. It can reduce the times of dilution and the error introduced by the dilution, and improve the accuracy of determination results of rubidium. Through analyzing the sensitivity of the three detection spectral lines for rubidium ion, linearly dependent coefficient and the relative errors of the determination results, the spectral line of Rb 780. 023 nm was chosen as the most suitable wavelength to measure the high content of rubidium in the rubidium chloride solutions. It was found that the instrument parameters of ICP-OES such as the atomizer flow, the pump speed and the high-frequency power are the major factors for the determination of rubidium ion in the rubidium chloride solutions. As we know instrument parameters of ICP-OES have an important influence on the atomization efficiency as well as the emissive power of the spectral lines of rubidium, they are considered as the significant factors for the determination of rubidium. The optimization parameters of the instrument were obtained by orthogonal experiments and further single factor experiment, which are 0. 60 L . min-1 of atomizer flow, 60 r . min-1 of pump speed, and 1 150 W of high-frequency power. The same experiments were repeated a week later with the optimization parameters of the instrument, and the relative errors of the determination results are less than 0. 5% when the concentration of rubidium chloride ranged from 0. 09% to 0. 18%. As the concentration of rubidium chloride is 0. 06%, the relative errors of the determination results are -1. 7%. The determination of lithium chloride and potassium chloride in the high concentration of the aqueous solutions was studied under the condition of similar instrument parameters. It was found by comparison that the determination results of lithium

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

    NASA Technical Reports Server (NTRS)

    Furton, Douglas G.; Witt, Adolf N.

    1993-01-01

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

  1. Simulation of field-induced molecular dissociation in atom-probe tomography: Identification of a neutral emission channel

    NASA Astrophysics Data System (ADS)

    Zanuttini, David; Blum, Ivan; Rigutti, Lorenzo; Vurpillot, François; Douady, Julie; Jacquet, Emmanuelle; Anglade, Pierre-Matthieu; Gervais, Benoit

    2017-06-01

    We investigate the dynamics of dicationic metal-oxide molecules under large electric-field conditions, on the basis of ab initio calculations coupled to molecular dynamics. Applied to the case of ZnO2 + in the field of atom probe tomography (APT), our simulation reveals the dissociation into three distinct exit channels. The proportions of these channels depend critically on the field strength and on the initial molecular orientation with respect to the field. For typical field strength used in APT experiments, an efficient dissociation channel leads to emission of neutral oxygen atoms, which escape detection. The calculated composition biases and their dependence on the field strength show remarkable consistency with recent APT experiments on ZnO crystals. Our work shows that bond breaking in strong static fields may lead to significant neutral atom production, and therefore to severe elemental composition biases in measurements.

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

    NASA Technical Reports Server (NTRS)

    Furton, Douglas G.; Witt, Adolf N.

    1993-01-01

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

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

    NASA Technical Reports Server (NTRS)

    Ingebo, R. D.

    1980-01-01

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

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

    NASA Astrophysics Data System (ADS)

    Gullberg, Bitten

    2016-03-01

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

  5. Determination of antimony, arsenic, bismuth and copper by inductively coupled plasma atomic emission spectrometry in the electrorefining of copper.

    PubMed

    Piippanen, T; Tummavuori, J

    1996-08-01

    Inductively coupled plasma atomic emissionspectrometry (ICP-AES) has been applied as a rapid and routine method for the analysis of process electrolytes in the electrorefining of copper. Antimony, arsenic, bismuth and copper have been selected as major electrolyte constituents. For these elements profound statistical studies of spectral and interelement effects have been carried out. For As, Bi and Sb two analyte wavelengths have been selected, and for Cu one relatively insensitive analyte line has been chosen due to the high Cu concentration in samples. Best analytical lines were: As at 193.759 nm, Bi at 306.772 nm, Sb at 206.833 nm and Cu at 216.953 nm. Multiple linear regression proved to be very capable in the search of the best analytical wavelength and identifying interfering elements. Using simple acid based standards all elements investigated can be determined separately in complicated matrices with satisfactory results. Differences between true values and measured values can be partly eliminated by appropriate calculational methods.

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

    NASA Technical Reports Server (NTRS)

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

    1972-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1972-01-01

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

  8. Effect of composition of electrolyte cathode on emission intensity of metal atoms in the discharge plasma at atmospheric pressure

    NASA Astrophysics Data System (ADS)

    Sirotkin, N. A.; Titov, V. A.

    2017-01-01

    The emission spectra and the plasma parameters of discharges were investigated. Water solutions of copper and nickel chlorides with additions of sodium chloride were used as electrolyte cathodes. The change of the relative intensities of the emission lines of the elements (Cu and Ni) with increasing NaCl concentrations in the solution is shown. The gas temperature and the reduced electric field strength in the plasma were founded. The electron energy distribution function and the excitation rate coefficients for emitting states of copper and nickel atoms by the numerical solution of the Boltzmann equation were obtained. It was shown that in plasma emission spectroscopy measuring it is necessaryto considerthe correlation between rates of excitation and composition of the sample solution in order to determine the concentration of metal ions in the water solutions.

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

    NASA Astrophysics Data System (ADS)

    Leonovich, Ludmila; Leonovich, Vitaly; Tashchilin, Anatoly

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

  10. Low-Altitude Emission of Energetic Neutral Atoms: A New Diagnostic of the Energetics of Ion Precipitation

    NASA Astrophysics Data System (ADS)

    Roelof, E. C.; Nair, H.

    2010-12-01

    We describe a new theoretical understanding of the emission of energetic neutral atoms (ENAs) generated by the precipitation of energetic magnetospheric ions into the Earth’s monatomic oxygen (O) exosphere (200-800 km). This low altitude emission (LAE) is the brightest ENA source in images obtained from Astrid-1/PIPPI, IMAGE/MENA/HENA, and TWINS1/2. The upward ENA “albedo” from the precipitating protons in the energy range 1-100 keV can approach 50% of the incident proton intensity. Unlike FUV imaging, ENA imaging of the LAE allows us to extract the detailed (not integrated) energy spectrum of the precipitating protons. We have verified this claim by comparing ENA images from TWINS 1/2 with in situ ion spectra measured by DMSP spacecraft (~825 km altitude) flying simultaneously under the ENA LAE regions (Bazell et al., J. Geophys. Res., in press 2010, and also this Conference). Quantitative extraction of proton spectra from the ENA images requires a “thick-target” theory that treats properly the multiple atomic collisions (charge exchange of protons, stripping ENA H-atoms) and associated energy losses (including ionization and excitation). Analytic solutions to the coupled proton/H-atom transport equations have been obtained, and they provide quantitative insight into the strong dependence of the ENA LAE upon the pitch angle and the energy of the precipitating protons. Since global ENA images of LAE can be obtained with exposure times of a minute or so during large geomagnetic storms, the distribution in magnetic latitude and local time of their evolving spectra contain critical diagnostics of the physics of not only the precipitation process, but also of the acceleration of the energetic ions themselves. Simulated 24 keV ENA low altitude emission viewed from TWINS-2 generated by precipitating protons below a DMSP pass (Bazell et al., JGR, in press, 2010).

  11. ICP OES and CV AAS in determination of mercury in an unusual fatal case of long-term exposure to elemental mercury in a teenager.

    PubMed

    Lech, Teresa

    2014-04-01

    In this work, a case of deliberate self-poisoning is presented. A 14-year-old girl suddenly died during one of the several hospitalizations. Abdominal computer tomography showed a large number of metallic particles in the large intestine. Analysis of blood and internal organs for mercury and other toxic metals carried out by inductively coupled plasma optical emission spectrometry (ICP OES) revealed high concentrations of mercury in kidneys and liver (64,200 and 2470ng/g, respectively), less in stomach (90ng/g), and none in blood. Using cold vapor-atomic absorption spectrometry (CV AAS), high levels of mercury were confirmed in all examined materials, including blood (87ng/g), and additionally in hair. The results of analysis obtained by two techniques revealed that the exposure to mercury was considerable (some time later, it was stated that the mercury originated from thermometers that had been broken over the course of about 1 year, because of Münchausen syndrome). CV AAS is a more sensitive technique, particularly for blood samples (negative results using ICP OES), and tissue samples - with LOQ: 0.63ng/g of Hg (CV AAS) vis-à-vis 70ng/g of Hg (ICP OES). However, ICP OES may be used as a screening technique for autopsy material in acute poisoning by a heavy metal, even one as volatile as mercury.

  12. Cooperative spontaneous emission of N atoms: Many-body eigenstates, the effect of virtual Lamb shift processes, and analogy with radiation of N classical oscillators

    SciTech Connect

    Svidzinsky, Anatoly A.; Chang, J.-T.; Scully, Marlan O.

    2010-05-15

    We consider collective emission of a single photon from a cloud of N two-level atoms (one excited, N-1 ground state). For a dense cloud the problem is reduced to finding eigenfunctions and eigenvalues of an integral equation. We discuss an exact analytical solution of this many-atom problem for a spherically symmetric atomic cloud. Some eigenstates decay much faster then the single atom decay rate, while the others undergo very slow decay. We show that virtual processes yield a small effect on the evolution of rapidly decaying states. However, they change the long time dynamics from exponential decay into a power-law behavior which can be observed experimentally. For trapped states virtual processes are much more important yielding additional decay channels which results in a slow decay of the otherwise trapped states. We also show that quantum mechanical treatment of spontaneous emission of weakly excited atomic ensemble is analogous to emission of N classical harmonic oscillators.

  13. Method 200.7: Determination of Metals and Trace Elements in Water and Wastes by Inductively Coupled Plasma-Atomic Emission Spectrometry

    EPA Pesticide Factsheets

    SAM lists this method for preparation and analysis of aqueous liquid and drinking water samples. This method will determine metal-containing compounds as the total metal (e.g., total arsenic), using inductively coupled plasma-atomic emission spectrometry.

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

    NASA Technical Reports Server (NTRS)

    Bauman, Leslie E.

    1990-01-01

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

  15. ICP-AES Determination of Mineral Content in Boletus tomentipes Collected from Different Sites of China.

    PubMed

    Wang, Xue-mei; Zhang, Ji; Li, Tao; Li, Jie-qing; Wang, Yuan-zhong; Liu, Hong-gao

    2015-05-01

    P, Na, Ca, Cu, Fe, Mg, Zn, As, Cd, Co, Cr and Ni, contents have been examined in caps and stipes of Boletus tomentipes collected from different sites of Yunnan province, southwest China. The elements were determined using inductively coupled plasma atomic emission spectroscopy (ICP-AES) with microwave digestion. P, Ca, Mg, Fe, Zn and Cu were the most abundant amongst elements determined in Boletus tomentipes. The caps were richer in P, Mg, Zn and Cd, and the stipes in Ca, Co and Ni. Cluster analysis showed a difference between Puer (BT7 and BT8) and other places. The PCA explained about 77% of the total variance, and the minerals differentiating these places were P (PC1) together with Ca, Cu, Fe, Mg, As and Ni, Na (PC2) together with Cd, and Zn (PC3). The results of this study imply that element concentrations of a mushroom are mutative when collected from the different bedrock soil geochemistry.

  16. Evaluation of inorganic elements in cat's claw teas using ICP OES and GF AAS.

    PubMed

    Pereira, João B; Dantas, Kelly G F

    2016-04-01

    The determination of Ba, Ca, Cu, Fe, Mg, Mn, P, Pb, and Zn by inductively coupled plasma optical emission spectrometry (ICP OES), and Se by graphite furnace atomic absorption spectrometry (GF AAS), has been carried out in dry matter and teas from 11 samples of the cat's claw plant. The accuracy and precision values were verified against GBW 07604 (Poplar leaves) certified reference material and by the recovery test. Results showed a high content of Ca in the medicinal plant studied, followed by Mg and P. The values obtained showed that the elements studied have different concentrations depending on the method of tea preparation. The highest levels were observed in Ca and Mg, and the lowest for Se and Pb, by both infusion and decoction. Teas prepared from this plant were found to be at safe levels for human consumption, and may be suitable as sources of these elements in the human diet. Copyright © 2015 Elsevier Ltd. All rights reserved.

  17. Application of ICP-SFMS, ICP-AES integrate method to the geochemical characterization of ANDRILL-MIS oceanic sediment samples

    NASA Astrophysics Data System (ADS)

    Rugi, F.; Castellano, E.; Marino, F.; Ghedini, C.; Severi, M.; Becagli, S.; Traversi, R.; Udisti, R.

    2009-12-01

    An integrated system for the determination of 39 major and trace (including Rare Earths Elements -REE) metals in soils and marine sediments was set up by using Inductively Coupled Plasma - Sector Field Mass Spectrometry (ICP-SFMS) and Inductively Coupled Plasma - Atomic Emission Spectrophotometry (ICP - AES) devices, in order to achieve an extensive geochemical characterization. Major elements, in particular silicon, are also quantified with PIXE technique. Method selectivity, accuracy and reproducibility was evaluated analyzing six certified materials: Basalt, Hawaiian Volcanic Observatory (BHVO-1); Japanese Andesite (JA-2); Montana Soil (NIST 2711); Antarctic Sediment (CRM-MURST-ISS-A1); Antarctic Sediment (GBW 073113) e Antarctic Sediment (NIST 2702); after mineralization with fluoridric, nitric and perchloric acids on hot plate. The choice of the isotope (ICP-SFMS) or wavelength (ICP-AES) was addressed obtaining the best compromise between high sensitivity and suitable selectivity for the metal determination. Particular care was paid in optimizing analytical quantification of each species, because of the huge difference in concentration of major and trace elements in geological samples. For ICP-SFMS, high resolution (10,000 m/Δm) was selected for all metals to avoid isobaric interferences. An accurate blank evaluation was carried out, especially for metals present at sub-ppb levels in the extract solutions (REE and other trace elements). The obtained operative blank values included sample manipulation and digestion, reagent content and analytical procedures. ICP-SFMS and ICP-AES methods were applied to the characterization of the geochemical composition of sample from the first 90 m of Mc Murdo Ice Shelf (MIS) marine core, in the framework of the ANDRILL (ANtarctic DRILLing) Project. This international project aims to study the role of the Antarctic Continent within the global climatic system, by the recovery and analysis of two deep sediment cores (named MIS

  18. A non-element-enriched, non-lyophilized candidate rat serum reference material prepared for once use in determination of inorganic elements by ICP-MS.

    PubMed

    Li, Xiang-Yun; Lian, Hong-Zhen; Mao, Li; Chen, Yi-Jun; Hu, Xin; Qiao, Jun-qin; Sheng, Dong

    2009-06-15

    A practice about preparing a once-used native state candidate rat serum reference material has been described for inductively coupled plasma atomic emission spectrometry (ICP-MS) determination of inorganic elements in biological matrices, which is independently packed, easy to use, non-lyophilized, without element-spiking, and with stable quality. Various dispersing and storing factors influencing the serum quality have been investigated including container material, sampling volume, packing mode and storage time. The contents of twelve main elements in the rat serum have been not only evaluated by ICP-MS but also verified by other analytical techniques. The probation of this unconventional candidate serum reference material by different laboratories has given very similar contents of 12 main trace elements in the serum, and proven its applicability to support quality assurance of biological sample analyses.

  19. THAM for control of ICP.

    PubMed

    Zeiler, F A; Teitelbaum, J; Gillman, L M; West, M

    2014-10-01

    Our goal was to perform a systematic review of the literature on the use of tromethamine (THAM) and its effects on intracranial pressure (ICP) in patients with neurological illness. All articles from MEDLINE, BIOSIS, EMBASE, Global Health, HealthStar, Scopus, Cochrane Library, the International Clinical Trials Registry Platform (inception to February 2014), reference lists of relevant articles, and gray literature were searched. Two reviewers independently identified all manuscripts pertaining to the administration of THAM in human patients that recorded effects on ICP. Secondary outcomes of effect on cerebral perfusion pressure, mean arterial pressure, patient outcome, and adverse effects were recorded. Two reviewers independently extracted data including population characteristics and treatment characteristics. The strength of evidence was adjudicated using both the Oxford and GRADE methodology. Our search strategy produced a total 2,268 citations. Twelve articles, 9 manuscripts, and 3 meeting proceedings were considered for the review with all utilizing THAM while documenting ICP in neurosurgical patients. All studies were prospective. Across all studies, there were a total of 488 patients studied, with 263 receiving THAM and 225 serving as controls in a variety of heterogeneous studies. All but one study documented a decrease in ICP with THAM administration, with both bolus and continuous infusions. One study documented a reduction in cerebral perfusion pressure. No significant renal dysfunction, hepatocellular injury, or hypoglycemia were reported. Three prospective randomized control trials displayed trends to improved outcome in severe traumatic brain injury (TBI) patients with THAM administration. There currently exists Oxford level 2b, GRADE B evidence to support that THAM reduces ICP in the TBI and malignant ischemic infarct population, with minimal side effects. The literature suggests THAM may be useful for ICP reduction in certain cases, though the

  20. Middle- and low-latitude emissions from energetic neutral atom precipitation seen from ATLAS 1 under quiet magnetic conditions

    NASA Technical Reports Server (NTRS)

    Tinsley, B. A.; Rohrbaugh, R. P.; Ishimoto, M.; Torr, M. R.; Torr, D. G.

    1994-01-01

    During the ATLAS 1 mission spectral observations were made at middle and low latitudes of features expected from the precipitation of energetic neutral atoms. The Imaging Spectrometric Observatory was used at night in the UV and visible with maximum gain. The tangent ray heights of the look directions ranged from near 100 km to near 200 km, and the geomagnetic conditions were quiet during the observations, which were made March 28 to April 3, 1992. The N2(+) 1N 391.4-nm and O I 130.4 and 135.6-nm emissions were observed at all latitudes, with lower emission rates at lower magnetic dip latitudes, except that enhancements in the O I lines were seen within 30 deg of the dip equator to radiative recombination of ionospheric plasma. The latitude profile observed for the N2(+) 1N emission did not show an equatorial or midlatitude peak. This implies that the source of energetic neutrals is more consistent with prompt charge exchange loss of freshly injected trapped ions with relatively low mirror heights (i.e., ions on higher L shells with equatorial pitch angle distributions nearly isotropic to the loss cone) than loss of highly eroded populations of particles with high mirror heights (i.e., ions on lower L shells with pancake equatorial pitch angle distributions). The N2(+) 1N emission rates have been compared with models of atmospheric emission due to fluxes of O/O(+) and H/H(+) in the thermosphere, as produced by energetic neutral oxygen or hydrogen atom precipitation. Energy deposition rates are inferred.

  1. Characterization of helium/argon working gas systems in a radiofrequency glow discharge atomic emission source. Part I: Optical emission, sputtering and electrical characteristics

    NASA Astrophysics Data System (ADS)

    Christopher, Steven J.; Hartenstein, Matthew L.; Marcus, R. Kenneth; Belkin, Mikhail; Caruso, Joseph A.

    1998-08-01

    Studies are performed to determine the influence of discharge gas composition (helium/argon working gas mixtures) on the analyte emission signal intensities, sputtering rates, and DC-bias characteristics of an analytical radiofrequency glow discharge atomic emission spectroscopy (RF-GD-AES) source. As the partial pressure of He is increased from 0 to 15 torr, increased emission intensity is observed for a range of bulk and trace elements in NIST 1250 SRM (low alloy steel), regardless of the base pressure of Ar in the source (5 and 9 torr). In contrast to increases in analyte emission intensity of up to 300%, counterindicative decreases in the sputtering rates on the order of about 30-50% are observed. The magnitude of these effects depends on both the partial pressure of helium introduced to the source and the total pressure of the He and Ar gases. Use of relative emission yield (REY) to normalize changes in emission intensity to sputtering rates indicates that excitation efficiencies increase under these conditions. Increases in average electron energy and temperature appear to control this response. Decreases in both analyte emission intensities and sputter rates occur with increasing He partial pressure when the total pressure in the cell remains fixed (11 torr in these studies). Emission yields for the fixed pressure, mixed gas plasmas decrease as the partial pressure of He (He/Ar ratio) in the RF-GD source increases. In this case, decreases in electron number densities appear to dictate the lower REYs. Measurement of DC-bias values at the sample surface provide understanding with respect to the observed changes in sputtering rates as well as suggest the origins of changes in plasma electron energetics. Use of a diamond stylus profilometer provides both the quantitative sputter rate information as well as qualitative insights into the use of mixed gas plasmas for enhanced depth profiling capabilities. The analyte emission characteristics of these mixed gas

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

    NASA Astrophysics Data System (ADS)

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

    2013-03-01

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

  3. Two-Photon Emission of a Hydrogenlike Atom with Photon Polarization and Electron Spin States Taken into Account

    NASA Astrophysics Data System (ADS)

    Skobelev, V. V.

    2017-02-01

    The process of two-photon emission ( Ze)* → ( Ze) + 2 γ of a hydrogenlike atom is considered with spin states of the electron and polarization of the photons taken into account, which had not been done before. A general expression for the probability of the process per unit time has been obtained for different polarization states of the photons with a formulation of hard and soft selection rules for the quantum numbers m and l. It is shown that by virtue of the established specifics of the properties of the two-photon emission process (absence of a Zeeman effect and dependence of the probability on the polarization states of the photons), it can in principle be identified against the background of single-photon emission ( Ze)* → ( Ze) + γ, despite the presence of additional small factors: 1) α = e 2/ ћc ≈ 1/137 of the perturbation theory in e, and 2) the square of the atomic expansion parameter ( Zα)2 in the expression for the probability.

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

    PubMed

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

    2004-02-18

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

  5. The calibration of XRF polyethylene reference materials with k0-NAA and ICP-AES

    NASA Astrophysics Data System (ADS)

    Swagten, Josefien; Bossus, Daniël; Vanwersch, Hanny

    2006-08-01

    Due to the lack of commercially available polyethylene reference materials for the calibration of X-ray fluorescence spectrometers (XRF), DSM Resolve, in cooperation with PANalytical, prepared and calibrated such a set of standards in 2005. The reference materials were prepared based on the addition of additives to virgin polyethylene. The mentioned additives are added to improve the performance of the polymers. The elements present in additives are tracers for the used additives. The reference materials contain the following elements: F, Na, Mg, Al, Si, P, S, Ca, Ti and Zn in the concentration range of 5 mg/kg for Ti, up to 600 mg/kg for Mg. The calibration of the reference materials, including a blank, was performed using inductively coupled plasma atomic emission spectrometry (ICP-AES) and Neutron Activation Analysis ( k0-NAA). ICP-AES was used to determine the elements Na, Mg, Al, P, Ca, Ti and Zn whereas k0-NAA was used for F, Na, Mg, Al, Ca, Ti and Zn. Over the complete concentration range, a good agreement of the results was found between the both techniques. This project has shown that within DSM Resolve, it is possible to develop and to calibrate homogenous reference materials for XRF.

  6. Spontaneous emission from a two-level atom in anisotropic one-band photonic crystals: A fractional calculus approach

    SciTech Connect

    Wu, J.-N.; Huang, C.-H.; Cheng, S.-C.; Hsieh, W.-F.

    2010-02-15

    Spontaneous emission (SE) from a two-level atom in an anisotropic photonic crystal (PC) is investigated by the fractional calculus. Physical phenomena of the SE are studied analytically by solving the fractional kinetic equations of the SE. There is a dynamical discrepancy between the SE of anisotropic and isotropic PCs. We find that, contrary to the SE phenomenon of the isotropic PC, the SE near the band edge of an anisotropic PC shows no photon-atom bound state. It is consistent with the experimental results of Barth, Schuster, Gruber, and Cichos [Phys. Rev. Lett. 96, 243902 (2006)] that the anisotropic property of the system enhances the SE. We also study effects of dispersion curvatures on the changes of the photonic density of states and the appearance of the diffusion fields in the SE.

  7. Identify the injury implements by SEM/EDX and ICP-AES.

    PubMed

    Bai, Rufeng; Wan, Lihua; Li, Hongwei; Zhang, Zhong; Ma, Zhihua

    2007-02-14

    The forensic investigator is frequently confronted with the discrimination and deduction of injury implements, which is one of the most important physical testimonies in courts. The usual method used in actual cases is from points of morphology. In the forensic discrimination of injury implements, such as metal implements, the analysis and comparison of elements are expected to provide excellent results, and simultaneous multi-elemental analysis is required to analyze various kinds of elements. This study was designed to establish discrimination and deduction of metal injury implements by scanning electron microscope/energy disperse X-ray microanalyzer (SEM/EDX) and inductively coupled plasma atomic emission spectrometry (ICP-AES). Examined metal particles in five wounds made on the skin of domestic pigs, respectively, using Cu-Zn or Cr-Ni coated and carbon steel kitchen implements by EDX. For carbon steel kitchen implements, analyzed five samples from the back and blade separately in the contents and varieties of elements by ICP-AES. In the wounds by the coated implements, the special particles only containing Cu, Zn or Cr, Ni were found. In the wounds by carbon steel kitchen implements, the particles containing Fe, Cr, Si or Fe, Mn, Si were found. The differences of contents of elements between the back and blade was no significant except No. 5 for carbon steel kitchen implements, and the significant differences of elements exited in Cr, Mn, Si, Cu, Mo among the stainless kitchen knives, Mn, Si among the other kitchen implements and for the blade of No. 5 knife, relative standard deviations (R.S.D.s) were significantly different in Mn, Si, Mo, Ti, S, P, Ni. Using EDX to examine the particles in wounds can deduce the categories of metal injury implements, and we can still deduce the different implements in the same category by ICP-AES.

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

    USGS Publications Warehouse

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

    1991-01-01

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

  9. Dislocation emission at the Silicon/Silicon nitride interface: A million atom molecular dynamics simulation on parallel computers

    PubMed

    Bachlechner; Omeltchenko; Nakano; Kalia; Vashishta; Ebbsjo; Madhukar

    2000-01-10

    Mechanical behavior of the Si(111)/Si(3)N4(0001) interface is studied using million atom molecular dynamics simulations. At a critical value of applied strain parallel to the interface, a crack forms on the silicon nitride surface and moves toward the interface. The crack does not propagate into the silicon substrate; instead, dislocations are emitted when the crack reaches the interface. The dislocation loop propagates in the (1; 1;1) plane of the silicon substrate with a speed of 500 (+/-100) m/s. Time evolution of the dislocation emission and nature of defects is studied.

  10. Dislocation Emission at the Silicon/Silicon Nitride Interface: A Million Atom Molecular Dynamics Simulation on Parallel Computers

    NASA Astrophysics Data System (ADS)

    Bachlechner, Martina E.; Omeltchenko, Andrey; Nakano, Aiichiro; Kalia, Rajiv K.; Vashishta, Priya; Ebbsjö, Ingvar; Madhukar, Anupam

    2000-01-01

    Mechanical behavior of the Si\\(111\\)/Si3N4\\(0001\\) interface is studied using million atom molecular dynamics simulations. At a critical value of applied strain parallel to the interface, a crack forms on the silicon nitride surface and moves toward the interface. The crack does not propagate into the silicon substrate; instead, dislocations are emitted when the crack reaches the interface. The dislocation loop propagates in the \\(1¯ 1¯1\\) plane of the silicon substrate with a speed of 500 \\(+/-100\\) m/s. Time evolution of the dislocation emission and nature of defects is studied.

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

    NASA Technical Reports Server (NTRS)

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

    1993-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1993-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1979-01-01

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

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

    SciTech Connect

    Sancho, Pedro; Plaja, Luis

    2011-06-15

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

  15. Collection of trace evidence of explosive residues from the skin in a death due to a disguised letter bomb. The synergy between confocal laser scanning microscope and inductively coupled plasma atomic emission spectrometer analyses.

    PubMed

    Turillazzi, Emanuela; Monaci, Fabrizio; Neri, Margherita; Pomara, Cristoforo; Riezzo, Irene; Baroni, Davide; Fineschi, Vittorio

    2010-04-15

    In most deaths caused by explosive, the victim's body becomes a depot for fragments of explosive materials, so contributing to the collection of trace evidence which may provide clues about the specific type of device used with explosion. Improvised explosive devices are used which contain "homemade" explosives rather than high explosives because of the relative ease with which such components can be procured. Many methods such as chromatography-mass spectrometry, scanning electron microscopy, stereomicroscopy, capillary electrophoresis are available for use in the identification of explosive residues on objects and bomb fragments. Identification and reconstruction of the distribution of explosive residues on the decedent's body may give additional hints in assessing the position of the victim in relation to the device. Traditionally these residues are retrieved by swabbing the body and clothing during the early phase, at autopsy. Gas chromatography-mass spectrometry and other analytical methods may be used to analyze the material swabbed from the victim body. The histological examination of explosive residues on skin samples collected during the autopsy may reveal significant details. The information about type, quantity and particularly about anatomical distribution of explosive residues obtained utilizing confocal laser scanning microscope (CLSM) together with inductively coupled plasma atomic emission spectrometer (ICP-AES), may provide very significant evidence in the clarification and reconstruction of the explosive-related events. Copyright 2009 Elsevier Ireland Ltd. All rights reserved.

  16. A novel methodology for rapid digestion of rare earth element ores and determination by microwave plasma-atomic emission spectrometry and dynamic reaction cell-inductively coupled plasma-mass spectrometry.

    PubMed

    Helmeczi, Erick; Wang, Yong; Brindle, Ian D

    2016-11-01

    Short-wavelength infrared radiation has been successfully applied to accelerate the acid digestion of refractory rare-earth ore samples. Determinations were achieved with microwave plasma-atomic emission spectrometry (MP-AES) and dynamic reaction cell - inductively coupled plasma-mass spectrometry (DRC-ICP-MS). The digestion method developed was able to tackle high iron-oxide and silicate matrices using only phosphoric acid in a time frame of only 8min, and did not require perchloric or hydrofluoric acid. Additionally, excellent recoveries and reproducibilities of the rare earth elements, as well as uranium and thorium, were achieved. Digestions of the certified reference materials OREAS-465 and REE-1, with radically different mineralogies, delivered results that mirror those obtained by fusion processes. For the rare-earth CRM OKA-2, whose REE data are provisional, experimental data for the rare-earth elements were generally higher than the provisional values, often exceeding z-values of +2. Determined values for Th and U in this reference material, for which certified values are available, were in excellent agreement.

  17. A Magnetized Nanoparticle Based Solid-Phase Extraction Procedure Followed by Inductively Coupled Plasma Atomic Emission Spectrometry to Determine Arsenic, Lead and Cadmium in Water, Milk, Indian Rice and Red Tea.

    PubMed

    Azimi, Salameh; Es'haghi, Zarrin

    2017-06-01

    A sensitive and simple method using magnetic multi-walled carbon nanotube (MWCNTs-Fe3O4 MNP), as the adsorbent, has been successfully developed for extraction and pre-concentration of arsenic, lead and cadmium with detection by inductively coupled plasma-atomic emission spectroscopy (ICP-AES). The nanosorbent was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction pattern (XRD), vibrating sample magnetometer (VSM) and transmission electron microscopy (TEM). The key factors affecting the signal intensity such as pH, adsorbent amount, etc. were investigated. Under optimal conditions, the limits of detection (three-time of signal to noise ratio, S/N 3) were 0.3, 0.6, 0.3 ng/mL for arsenic, lead and cadmium, respectively. Application of the adsorbent was investigated by the analysis of water, milk, Indian rice and red tea. The experimental data was analyzed and obeyed Langmuir and Freundlich adsorption models. The kinetic data was fitted to the pseudo-second-order model. Thermodynamic studies revealed the feasibility and exothermic nature of the system.

  18. Background correction in atomic emission spectrometry using repetitive harmonic wavelength scanning and applying Fourier analysis—I. Theory

    NASA Astrophysics Data System (ADS)

    Matthee, T.; Visser, K.

    1995-07-01

    Repetitive wavelength scanning can be used as a means of detecting and correcting for unwanted background in atomic emission spectrometry (AES). This paper deals with the theory underlying such harmonic wavelength scanning in time and stresses the relative importance of the relevant parameters. A set of integrated Turbo Pascal programs for an IBM PC was developed to provide a numerical simulation for the deconvolution of a detected spectral profile during repetitive harmonic wavelength scanning. By applying this numerical analysis the theory for separating the net spectral emission signal and the background radiation by filtering specific frequency components is investigated. It is concluded that, barring the dc component, repetitive scanning over a symmetric spectral profile leads to the generation of even-numbered Fourier harmonics at the modulation frequency, while an asymmetric spectral profile generates odd-numbered Fourier harmonics.

  19. Calculation of spontaneous emission from a V-type three-level atom in photonic crystals using fractional calculus

    SciTech Connect

    Huang, Chih-Hsien; Hsieh, Wen-Feng; Wu, Jing-Nuo; Cheng, Szu-Cheng; Li, Yen-Yin

    2011-07-15

    Fractional time derivative, an abstract mathematical operator of fractional calculus, is used to describe the real optical system of a V-type three-level atom embedded in a photonic crystal. A fractional kinetic equation governing the dynamics of the spontaneous emission from this optical system is obtained as a fractional Langevin equation. Solving this fractional kinetic equation by fractional calculus leads to the analytical solutions expressed in terms of fractional exponential functions. The accuracy of the obtained solutions is verified through reducing the system into the special cases whose results are consistent with the experimental observation. With accurate physical results and avoiding the complex integration for solving this optical system, we propose fractional calculus with fractional time derivative as a better mathematical method to study spontaneous emission dynamics from the optical system with non-Markovian dynamics.

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

    SciTech Connect

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

    2012-03-20

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

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

    NASA Astrophysics Data System (ADS)

    Bhardwaj, Anil; Raghuram, Susarla

    2012-03-01

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

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

    PubMed

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

    2014-03-26

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

  3. Mode transitions and electronegativity in oxygen CCP and ICP

    NASA Astrophysics Data System (ADS)

    Meichsner, Juergen; Wegner, Thomas

    2016-09-01

    Mode transitions in 13.56 MHz oxygen radio frequency plasmas (CCP, ICP) and their impact on the electron heating mechanisms and electronegativity were studied by advanced plasma diagnostics. In particular, Langmuir probe measurements, Gaussian beam microwave interferometry (160 GHz) coupled with laser photodetachment of negative oxygen ions, as well as the (phase resolved) optical emission and VUV absorption spectroscopy, and ion mass spectrometry are taken into consideration. With increasing RF power a transition between high and low electronegativity was found both in CCP and ICP discharge configuration. Thereby, the changed electron heating mechanisms, e.g., the alpha-gamma mode transition in CCP and the E-H mode transition in ICP is combined with the change of electronegativity. In strongly asymmetric CCP at moderate pressure the emission of secondary negative ions at the powered electrode have to be considered, too. Thereby, pseudo secondary electrons may be produced due to collision detachment of negative ion by metastables. During the E-H mode transition in oxygen ICP, the increasing gas temperature and the metastables influences significantly the oxygen kinetics. Supported by the DFG Collaborative Research Centre Transregio 24 ``Fundamentals of Complex Plasmas''.

  4. [Determination of heavy metals for RoHS compliance by ICP-OES spectrometry coupled with microwave extraction system].

    PubMed

    Hua, Li; Wu, Yi-Ping; An, Bing; Lai, Xiao-Wei

    2008-11-01

    The harm of heavy metals contained in electronic and electrical equipment (EEE) on environment is of high concern by human. Aiming to handle the great challenge of RoHS compliance, the determinations of trace or ultratrace chromium (Cr), cadmium (Cd), mercury (Hg) and lead (Pb) by inductively coupled plasma optical emission spectrometry (ICP-OES) was performed in the present paper, wherein, microwave extraction technology was used to prepare the sample solutions. In addition, the precision, recovery, repeatability and interference issues of this method were also discussed. The results exhibited that using the microwave extraction system to prepare samples is more quick, lossless, contamination-free in comparison with the conventional extraction methods such as dry ashing, wet-oven extraction etc. By analyzing the recoveries of these four heavy metals over different working time and wavelengths, the good recovery range between 85% and 115% showed that there was only tiny loss or contamination during the process of microwave extraction, sample introduction and ICP detection. Repeatability experiments proved that ICP plasma had a good stability during the working time and the matrix effect was small. Interference was a problem troublesome for atomic absorption spectrometry (AAS), however, the techniques of standard additions or inter-element correction (IEC) method can effectively eliminated the interferences of Ni, As, Fe etc. with the Cd determination. By employing the multi-wavelengths and two correction point methods, the issues of background curve sloping shift and spectra overlap were successfully overcome. Besides, for the determinations of trace heavy metal elements, the relative standard deviation (RSD) was less than 3% and the detection limits were less than 1 microg x L(-10 (3sigma, n = 5) for samples, standard solutions, and standard additions, which proved that ICP-OES has a good precision and high reliability. This provided a reliable technique support

  5. Fractionation and determination of aluminum and iron in soil water samples using SPE cartridges and ICP-AES.

    PubMed

    Tangen, Gaute; Wickstrøm, Torild; Lierhagen, Syverin; Vogt, Rolf; Lund, Walter

    2002-12-15

    The use of commercially available solid phase extraction (SPE) cartridges for the fractionation of Al and Fe in soil water is described. The quantitative determination was done by inductively coupled plasma atomic emission spectrometry (ICP-AES). Different types of SPE cartridges, based on cation exchange, anion exchange, and chelation were studied. To avoid pH changes, the SPE cartridge should be conditioned with a buffer that has a pH close to that of the sample. Both strong cation exchange (SCX) and chelation were found to work well, whereas low recovery was observed for Al when anion exchange was used. For Fe, the sum of the anionic and cationic fractions that passed through the cartridges was nearly 100%. The results obtained for Al for 23 soil water samples using a SPE/SCX cartridge and ICP-AES were compared with equilibrium calculations using the program ALCHEMI and also with a fractionation method that was based on separation on a manually prepared SCX column and detection by molecular spectrophotometry, after complexation with pyrocatechol violet (SCX-PCV method). The SPE/SCX-ICP-AES results for the labile Al fraction (Al bound to the SCX cartridge) showed an acceptable correlation with the results obtained by the equilibrium calculations, except for the samples with the highest DOC concentrations, whereas the values obtained for labile Al by the more traditional SCX-PCV method were much lower. We recommend that the SPE/SCX-ICP-AES procedure described in this work be selected for the fractionation of Al and Fe species in soil and freshwater samples.

  6. Study of gamma-ray emission by proton beam interaction with injected Boron atoms for future medical imaging applications

    NASA Astrophysics Data System (ADS)

    Petringa, G.; Cirrone, G. A. P.; Caliri, C.; Cuttone, G.; Giuffrida, L.; Larosa, G.; Manna, R.; Manti, L.; Marchese, V.; Marchetta, C.; Margarone, D.; Milluzzo, G.; Picciotto, A.; Romano, F.; Romano, F. P.; Russo, A. D.; Russo, G.; Santonocito, D.; Scuderi, V.

    2017-03-01

    In this work an experimental and theoretical study of gamma-prompt emission has been carried out with the main aim being to understand to what extent this approach can be used during a treatment based on proton-boron fusion therapy. An experimental campaign, carried out with a high purity Germanium detector, has been performed to evaluate the gamma emission from two pure 11B and 10B targets. Furthermore, a set of analytical simulations, using the Talys nuclear reaction code has been performed and the calculated spectra compared with the experimental results. These comparisons allowed us to successfully validate Talys which was then used to estimate the gamma emission when a realistic Boron concentration was considered. Both simulations and experimental results suggest that the gamma emission is low at certain proton energies, thus in order to improve the imaging capabilities, while still maintaining the Boron therapeutic role, we propose the addition of natural Copper bound by a dipyrromethene, BodiPy, to boron atoms. Analytical simulations with Talys suggest that the characteristic spectrum of the copper prompt gamma-rays has several peaks in the energetic regions where the background is negligible.

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

    SciTech Connect

    Bulanov, Alexey V.; Nagorny, Ivan G.

    2015-10-28

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

  8. Determination of trace elements in heroin by inductively coupled plasma atomic emission spectrometry using ultrasonic nebulization

    NASA Astrophysics Data System (ADS)

    Budič, Bojan; Klemenc, Sonja

    2000-06-01

    A method for the determination of Al, Ba, Ca, Cu, Fe, K, Mg, Mn, Na, Ni, P, S, Sr and Zn in heroin samples by ICP-AES using ultrasonic nebulization is described. The samples were microwave digested with HNO 3. To improve the detection limits and minimise the matrix interferences the experimental parameters were optimised by variation of the operating power, carrier gas flow rate and observation height above the load coil. Optimum operating conditions for most of the analytes were at operating power 1550 W, carrier gas flow rate between 0.8 and 1.0 l min -1 and observation height between 10 and 12 mm above load coil. The limits of detection were below 0.5 μg g -1 (dry mass) for most of the elements investigated. The analytical recoveries of spiked samples were in the range between 94 and 103% and precision was on average better than 6%. The analysis of heroin samples shows that the method is simple, rapid and capable of providing accurate results for all the analytes investigated with the exception of nickel which was below the limit of detection in the analyzed samples.

  9. Quantum theory of two-photon correlated-spontaneous-emission lasers: Exact atom-field interaction Hamiltonian approach

    SciTech Connect

    Lu, N.; Zhu, S. )

    1989-11-15

    A quantum theory of two-photon correlated-spontaneous-emission lasers (CEL's) is developed, starting from the exact atom-field interaction Hamiltonian for cascade three-level atoms interacting with a single-mode radiation field. We consider the situation where the active atoms are prepared initially in a coherent superposition of three atomic levels and derive a master equation for the field-density operator by using a quantum theory for coherently pumped lasers. The master equation is transformed into a Fokker-Planck equation for the antinormal-ordering {ital Q} function. The drift coefficients of the Fokker-Planck equation enable us to study the steady-state operation of the two-photon CEL's analytically. We have studied both resonant two-photon CEL for which there is no threshold, and off-resonant two-photon CEL for which there exists a threshold. In both cases the initial atomic coherences provide phase locking, and squeezing in the phase quadrature of the field is found. The off-resonant two-photon CEL can build up from a vacuum when its linear gain is larger than the cavity loss (even without population inversion). Maximum squeezing is found in the no-population-inversion region with the laser intensities far below saturation in both cases, which are more than 90% for the resonant two-photon CEL and nearly 50% for the off-resonant one. Approximate steady-state {ital Q} functions are obtained for the resonant two-photon CEL and, in certain circumstances, for the off-resonant one.

  10. Anisotropic emission of neutral atoms: evidence of an anisotropic Rydberg sheath in nanoplasma

    NASA Astrophysics Data System (ADS)

    Rajeev, R.; Madhu Trivikram, T.; Rishad, K. P. M.; Krishnamurthy, M.

    2015-02-01

    Intense laser-produced plasma is a complex amalgam of ions, electrons and atoms both in ground and excited states. Little is known about the spatial composition of the excited states that are an integral part of most gaseous or cluster plasma. In cluster-plasma, Rydberg excitations change the charge composition of the ions through charge transfer reactions and shape the angular distributions. Here, we demonstrate a non-invasive technique that reveals the anisotropic Rydberg excited cluster sheath by measuring anisotropy in fast neutral atoms. The sheath is stronger in the direction of light polarization and the enhanced charge transfer by the excited clusters results in larger neutralization.

  11. Influence of binders on infrared laser ablation of powdered tungsten carbide pressed pellets in comparison with sintered tungsten carbide hardmetals studied by inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Holá, Markéta; Otruba, Vítězslav; Kanický, Viktor

    2006-05-01

    Laser ablation (LA) was studied as a sample introduction technique for the analysis of powdered and sintered tungsten carbides (WC/Co) by inductively coupled plasma optical emission spectrometry (ICP-OES). The possibility to work with powdered and compact materials with close chemical composition provided the opportunity to compare LA sampling of similar substances in different forms that require different preparation procedures. Powdered WC/Co precursors of sintered hardmetals were prepared for the ablation as pressed pellets with and without powdered silver as a binder, while sintered hardmetal blocks were embedded into a resin to obtain discs, which were then smoothed and polished. A Q-switched Nd:YAG laser operated at its fundamental wavelength of 1064 nm with a pulse frequency of 10 Hz and maximum pulse energy of 220 mJ was used. A single lens was used for the laser beam focusing. An ablation cell (14 cm 3) mounted on a PC-controlled XY-translator was connected to an ICP spectrometer Jobin Yvon 170 Ultrace (laterally viewed ICP, mono- and polychromator) using a 1.5-m tubing (4 mm i.d.). Ablation was performed in a circular motion (2 mm diameter). Close attention was paid to the study of the crater parametres depending on hardness, cohesion and Ag binder presence in WC/Co samples. The influence of the Co content on the depth and structure of the ablation craters of the binderless pellets was also studied. Linear calibration plots of Nb, Ta and Ti were obtained for cemented WC/Co samples, binderless and binder-containing pellets. Relative widths of uncertainty intervals about the centroids vary between ± 3% and ± 7%, and exceptionally reach a value above 10%. The lowest determinable quantities (LDQ) of Nb, Ta and Ti calculated from the calibration lines were less than 0.5% (m/m). To evaluate the possibility of quantitative elemental analysis by LA-ICP-OES, two real sintered WC/Co samples and two real samples of powdered WC/Co materials were analysed. The

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

    SciTech Connect

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

    2013-02-15

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

  13. The design and characteristics of direct current glow discharge atomic emission source operated with plain and hollow cathodes.

    PubMed

    Qayyum, A; Mahmood, M I

    2008-01-07

    A compact direct current glow discharge atomic emission source has been designed and constructed for analytical applications. This atomic emission source works very efficiently at a low-input electrical power. The design has some features that make it distinct from that of the conventional Grimm glow discharge source. The peculiar cathode design offered greater flexibility on size and shape of the sample. As a result the source can be easily adopted to operate in Plain or Hollow Cathode configuration. I-V and spectroscopic characteristics of the source were compared while operating it with plain and hollow copper cathodes. It was observed that with hollow cathode, the source can be operated at a less input power and generates greater Cu I and Cu II line intensities. Also, the intensity of Cu II line rise faster than Cu I line with argon pressure for both cathodes. But the influence of pressure on Cu II lines was more significant when the source is operated with hollow cathode.

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

    NASA Astrophysics Data System (ADS)

    Ivanjek, L.; Shaffer, P. S.; McDermott, L. C.; Planinic, M.; Veza, D.

    2015-01-01

    This is the first of two closely related articles (Paper I and Paper II) that together illustrate how research in physics education has helped guide the design of instruction that has proved effective in improving student understanding of atomic spectroscopy. Most of the more than 1000 students who participated in this four-year investigation were science majors enrolled in the introductory calculus-based physics course at the University of Washington (UW) in Seattle, WA, USA. The others included graduate and undergraduate teaching assistants at UW and physics majors in introductory and advanced physics courses at the University of Zagreb, Zagreb, Croatia. About half of the latter group were preservice high school physics teachers. This article (Paper I) describes how several serious conceptual and reasoning difficulties were identified among students as they tried to relate a discrete line spectrum to the energy levels of atoms in a light source. Paper II illustrates how findings from this research informed the development of a tutorial that led to significant improvement in student understanding of atomic emission spectra.

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

    NASA Astrophysics Data System (ADS)

    Ivanjek, L.; Shaffer, P. S.; McDermott, L. C.; Planinic, M.; Veza, D.

    2015-02-01

    This is the second of two closely related articles (Paper I and Paper II) that together illustrate how research in physics education has helped guide the design of instruction that has proved effective in improving student understanding of atomic spectroscopy. Most of the more than 1000 students who participated in this four-year investigation were science majors enrolled in the introductory calculus-based physics course at the University of Washington (UW) in Seattle, WA, USA. The others included graduate and undergraduate teaching assistants at UW and physics majors in introductory and advanced physics courses at the University of Zagreb, Zagreb, Croatia. About half of the latter group were preservice high school physics teachers. Paper I describes how several conceptual and reasoning difficulties were identified among university students as they tried to relate a discrete line spectrum to the energy levels of atoms in a light source. This second article (Paper II) illustrates how findings from this research informed the development of a tutorial that led to improvement in student understanding of atomic emission spectra.

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

    NASA Technical Reports Server (NTRS)

    Smith, R. E.

    1976-01-01

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

  17. Effects of nozzle lip geometry on spray atomization and emissions advanced gas turbine combustors

    NASA Technical Reports Server (NTRS)

    Micklow, Gerald J.; Roychoudhury, Subir; Nguyen, H. L.

    1991-01-01

    A parametric study is conducted to investigate the effect of nozzle lip geometry on nozzle fuel distribution, emissions and temperature distribution for a rich burn section of a rich burn/quick quench/lean burn combustor. It is seen that the nozzle lip geometry greatly affects the fuel distribution, emissions and temperature distribution. It is determined that at an equivalence ratio of 1.6 the NO concentration could be lowered by a factor greater than three by changing the nozzle lip geometry.

  18. [Development of ICP-OES, ICP-MS and GF-AAS Methods for Simultaneous Quantification of Lead, Total Arsenic and Cadmium in Soft Drinks].

    PubMed

    Kataoka, Yohei; Watanabe, Takahiro; Hayashi, Tomoko; Teshima, Reiko; Matsuda, Rieko

    2015-01-01

    In this study, we developed methods to quantify lead, total arsenic and cadmium contained in various kinds of soft drinks, and we evaluated their performance. The samples were digested by common methods to prepare solutions for measurement by ICP-OES, ICP-MS and graphite furnace atomic absorption spectrometry (GF-AAS). After digestion, internal standard was added to the digestion solutions for measurements by ICP-OES and ICP-MS. For measurement by GF-AAS, additional purification of the digestion solution was conducted by back-extraction of the three metals into nitric acid solution after extraction into an organic solvent with ammonium pyrrolidine dithiocarbamate. Performance of the developed methods were evaluated for eight kinds of soft drinks.

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

    NASA Astrophysics Data System (ADS)

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

    2015-10-01

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

  20. Controlled single-photon emission from a single trapped two-level atom.

    PubMed

    Darquié, B; Jones, M P A; Dingjan, J; Beugnon, J; Bergamini, S; Sortais, Y; Messin, G; Browaeys, A; Grangier, P

    2005-07-15

    By illuminating an individual rubidium atom stored in a tight optical tweezer with short resonant light pulses, we created an efficient triggered source of single photons with a well-defined polarization. The measured intensity correlation of the emitted light pulses exhibits almost perfect antibunching. Such a source of high-rate, fully controlled single-photon pulses has many potential applications for quantum information processing.

  1. Statistical properties of spontaneous emission from atoms near a rough surface

    SciTech Connect

    Biehs, S.-A.; Greffet, J.-J.

    2011-11-15

    We study the lifetime of the excited state of an atom or molecule near a plane surface with a given random surface roughness. In particular, we discuss the impact of the scattering of surface modes within the rough surface. Our study is completed by considering the lateral correlation length of the decay rate and the variance discussing its relation to the C{sub 0} correlation.

  2. Efficient emission of positronium atoms from an Na-coated polycrystalline tungsten surface

    NASA Astrophysics Data System (ADS)

    Terabe, H.; Iida, S.; Wada, K.; Hyodo, T.; Yagishita, A.; Nagashima, Y.

    2013-06-01

    Time-of-flight spectra for the ortho-positronium emitted from clean and Na-coated tungsten surfaces have been measured using the pulsed slow positron beam at KEK-IMSS slow positron facility. Emission efficiency of positronium from the Na-coated sample was found to be several times greater than that from uncoated tungsten surfaces.

  3. Tunable and high-purity room temperature single-photon emission from atomic defects in hexagonal boron nitride.

    PubMed

    Grosso, Gabriele; Moon, Hyowon; Lienhard, Benjamin; Ali, Sajid; Efetov, Dmitri K; Furchi, Marco M; Jarillo-Herrero, Pablo; Ford, Michael J; Aharonovich, Igor; Englund, Dirk

    2017-09-26

    Two-dimensional van der Waals materials have emerged as promising platforms for solid-state quantum information processing devices with unusual potential for heterogeneous assembly. Recently, bright and photostable single photon emitters were reported from atomic defects in layered hexagonal boron nitride (hBN), but controlling inhomogeneous spectral distribution and reducing multi-photon emission presented open challenges. Here, we demonstrate that strain control allows spectral tunability of hBN single photon emitters over 6 meV, and material processing sharply improves the single photon purity. We observe high single photon count rates exceeding 7 × 10(6) counts per second at saturation, after correcting for uncorrelated photon background. Furthermore, these emitters are stable to material transfer to other substrates. High-purity and photostable single photon emission at room temperature, together with spectral tunability and transferability, opens the door to scalable integration of high-quality quantum emitters in photonic quantum technologies.Inhomogeneous spectral distribution and multi-photon emission are currently hindering the use of defects in layered hBN as reliable single photon emitters. Here, the authors demonstrate strain-controlled wavelength tuning and increased single photon purity through suitable material processing.

  4. Energetic particle imaging: The evolution of techniques in imaging high-energy neutral atom emissions

    NASA Astrophysics Data System (ADS)

    Mitchell, D. G.; Brandt, P. C.; Westlake, J. H.; Jaskulek, S. E.; Andrews, G. B.; Nelson, K. S.

    2016-09-01

    Energetic neutral atom imaging instruments have been flown on a variety of space missions to satisfy a variety of science requirements. In this paper we discuss the most recent developments that lead to improvements in energy range, angular resolution, and background rejection for the high-energy range, as represented in the past by the Cassini magnetosphere imaging instrument Ion and Neutral Camera, the Imager for Magnetopause-to-Aurora Global Exploration (IMAGE) mission High-Energy Neutral Atom instrument, and to some degree the IMAGE mission Medium-Energy Neutral Atom instrument. The new approaches discussed here rely on the use of ultrathin foils without UV filters and on very high speed coincidence logic to reduce accidentals from intense background sources. We present laboratory results demonstrating an electrostatic design that meets the coincidence timing requirements, position, and scattering performance consistent with angular resolution (full width at half maximum) of 2° for hydrogen above 10 keV and a hydrogen energy threshold ≤1 keV.

  5. Controlled Photon Emission and Raman Transition Experiments with a Single Trapped Atom

    NASA Astrophysics Data System (ADS)

    Jones, M. P. A.; Darquié, B.; Beugnon, J.; Dingjan, J.; Bergamini, S.; Sortais, Y.; Messin, G.; Browaeys, A.; Grangier, P.

    2005-12-01

    We present recent results on the coherent control of an optical transition in a single rubidium atom, trapped in an optical tweezer. We excite the atom using resonant light pulses that are short (4 ns) compared with the lifetime of the excited state (26 ns). By varying the intensity of the laser pulses, we can observe an adjustable number of Rabi oscillations, followed by free decay once the light is switched off. To generate the pulses we have developed a novel laser system based on frequency doubling a telecoms laser diode at 1560 nm. By setting the laser intensity to make a π pulse, we use this coherent control to make a high quality triggered source of single photons. We obtain an average single photon rate of 9600s-1 at the detector. Measurements of the second-order temporal correlation function show almost perfect antibunching at zero delay. In addition, we present preliminary results on the use of Raman transitions to couple the two hyperfine levels of the ground state of our trapped atom. This will allow us to prepare and control a qubit formed by two hyperfine sub-levels.

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

    PubMed

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

    2014-04-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2014-04-01

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

  8. Characterisation of Supra- and Infratentorial ICP Profiles.

    PubMed

    Moyse, Emmanuel; Ros, Maxime; Marhar, Fouad; Swider, Pascal; Schmidt, Eric Albert

    2016-01-01

    In pathophysiology and clinical practice, the intracranial pressure (ICP) profiles in the supratentorial and infratentorial compartments are unclear. We know that the pressure within the skull is unevenly distributed, with demonstrated ICP gradients. We recorded and characterised the supra- and infratentorial ICP patterns to understand what drives the transtentorial ICP gradient.A 70-year-old man was operated on for acute cerebellar infarction. One supratentorial probe and one cerebellar probe were implanted. Both signals were recorded concurrently and analysed off-line. We calculated mean ICP, ICP pulse amplitude, respiratory waves, slow waves and the RAP index of supra- and infratentorial ICP signals. Then, we measured transtentorial difference and performed correlation analysis for every index.Supratentorial ICP mean was 8.5 mmHg lower than infratentorial ICP, but the difference lessens for higher values. Both signals across the tentorium showed close correlation. Supra- and infratentorial pulse amplitude, respiratory waves and slow waves also showed a high degree of correlation. The compensatory reserve (RAP) showed good correlation. In this case report, we demonstrate that the mean value of ICP is higher in the posterior fossa, with a strong correlation across the tentorium. All other ICP-derived parameters display a symmetrical profile.

  9. Method validation for simultaneous determination of chromium, molybdenum and selenium in infant formulas by ICP-OES and ICP-MS.

    PubMed

    Khan, Naeem; Jeong, In Seon; Hwang, In Min; Kim, Jae Sung; Choi, Sung Hwa; Nho, Eun Yeong; Choi, Ji Yeon; Kwak, Byung-Man; Ahn, Jang-Hyuk; Yoon, Taehyung; Kim, Kyong Su

    2013-12-15

    This study aimed to validate the analytical method for simultaneous determination of chromium (Cr), molybdenum (Mo), and selenium (Se) in infant formulas available in South Korea. Various digestion methods of dry-ashing, wet-digestion and microwave were evaluated for samples preparation and both inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma mass spectrometry (ICP-MS) were compared for analysis. The analytical techniques were validated by detection limits, precision, accuracy and recovery experiments. Results showed that wet-digestion and microwave methods were giving satisfactory results for sample preparation, while ICP-MS was found more sensitive and effective technique than ICP-OES. The recovery (%) of Se, Mo and Cr by ICP-OES were 40.9, 109.4 and 0, compared to 99.1, 98.7 and 98.4, respectively by ICP-MS. The contents of Cr, Mo and Se in infant formulas by ICP-MS were found in good nutritional values in accordance to nutrient standards for infant formulas CODEX values.

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

    SciTech Connect

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

    1996-10-01

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

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

    SciTech Connect

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

    1996-03-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-08-01

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

  13. Design and characterization of a theta-pinch imploding thin film plasma source for atomic emission spectrochemical analysis.

    PubMed

    Navarre, Edward C; Goldberg, Joel M

    2011-01-01

    A new atomization device for direct atomic spectrochemical analysis has been developed that uses the theta-pinch configuration to generate a pulsed, high-energy-density plasma at atmospheric pressure. Energy from a 20-kV, 6.05-μF capacitive electrical discharge was inductively coupled to a sacrificial aluminum thin film to produce a cylindrical plasma. Current waveform analysis indicates an average power dissipation of 0.5 MW in the plasma. Electromagnetic modeling studies were used to identify theta-pinch designs possessing characteristics favorable to both plasma initiation and plasma heating. The discharge was most robust when the induced current and rate of magnetic field change were maximized. Minimizing the ratio of the coil's width to its radius was also critical. Counter to intuition, a larger diameter was found to be more successful. Spectroscopic studies indicate that the discharge forms a heterogeneous plasma with a dense, cylindrical plasma sheet confined by the walls of the discharge tube surrounding a less energetic plasma in the center. Al(II) emission in the outer plasma cylinder was temporally aligned with the induced current whereas in the center it aligns with the magnetic field. Ionization of support gas species (Ar, He, and air) was not observed, although the identity of the gas had a significant influence on the plasma reproducibility. The optimized design utilized a 5.5-turn, 19-mm-diameter theta coil with argon as the support gas. Sb(I) emission from an antimony oxide solid powder sample deposited on the thin film was observed primarily in the outer part of the plasma. Analyte emission shows contributions from magnetic compression early in the discharge and from the induced current late in the discharge. The discharge produced analytically useful signals from solid antimony oxide samples. Using spatially and temporally resolved detection, the line-to-background ratio for Sb(I) was found to be greater than 4 for emission integrated from 55

  14. Atomic emission spectrometric determination of ephedrine, cinchonine, chlorpheniramine, atropine and diphenhydramine based on formation of ion associates with ammonium reineckate.

    PubMed

    Khalil, S

    1999-12-01

    Ion-associate complexes of ephedrine HCl (I), cinchonine HCl (II), chlorpheniramine maleate (III), atropine sulphate (IV) and diphenhydramine HCl (V) with ammonium reineckate were precipitated and their solubilities were studied as a function of pH, ionic strength and temperature. Saturated solutions of each ion-associate under the optimum precipitation conditions were prepared and the Cr ion content in the supernatant was determined. The solubility products were thus elucidated at different temperatures. A new accurate and precise method using direct current plasma-atomic emission spectrometry for the determination of the investigated drugs in pure solutions and in pharmaceutical preparations is described. The drugs can determined by the present method in the ranges 1.6-52,2.64-85.8,3.12-101.4,5.52-180.4 and 2.72-75.85 microg/ml solutions of I, II, III, IV and V, respectively.

  15. Atom and molecule emission caused by ion impact into a frozen oxygen target: Role of rovibrational excitation

    NASA Astrophysics Data System (ADS)

    Anders, Christian; Pedrys, Roman; Urbassek, Herbert M.

    2013-11-01

    Translational energy distributions of particles sputtered by 750 eV Ne+ ion impact into a cryogenic O2 target are studied using molecular-dynamics simulation. When comparing the energy distribution of emitted molecules to a Thompson distribution, good agreement can only be found for energies E with Uemission. Around 2% of the sputtered particles consist of radicals (atomic O). These originate from direct projectile-molecule collisions; they are emitted early in the collision cascade and feature a strong high-energy contribution.

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

    NASA Astrophysics Data System (ADS)

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

    2003-03-01

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

  17. Three-phase plasma arc atomic-emission spectrometric analysis of environmental samples using an ultrasonic nebulizer.

    PubMed

    Ghatass, Zekry F; Roston, Gamal D; Mohamed, Moustafa M

    2003-06-01

    Combination of an ultrasonic nebulizer and plasma excitation sources for spectrochemical analysis offers desirable features of low detection limits, high sample throughput, wide dynamic range of operation, acceptable precision and accuracy, and simultaneous quantitative analytical capabilities. Moreover, the ultrasonic nebulizer does not require sample preconcentration. Recently we have developed a three-phase plasma arc (TPPA) for atomic emission spectrochemical analysis. In the present work, to increase the analytical utility of the three-phase plasma system, an ultrasonic nebulizer was used for sample introduction. The effects of the argon gas flow rate, current, excitation temperature have been studied. The analytical calibration curves are obtained for Ca, Cr, Fe, Mg and Mn, and detection limits have been calculated. The present technique is used to determine the concentration of the elements Ca, Cr, Fe, Mg and Mn in airborne samples.

  18. Analysis of sulfur-organic compounds in jet fuel by chromatographic sniffing and gas chromatography with atomic emission detector

    SciTech Connect

    Skoog, P.A.

    1995-04-01

    When the Swedish Air Force changed fuel from Jet B to Jet A-1 during 1991-1992, a working environmental problem was reported from the military air force bases. The symptoms were unpleasant odor, headache and indisposition. This problem arose from some batches of the new fuel, Jet A-1. In order to investigate the compounds in the fuel which gave rise to this problem a chromatographic sniffing technique (sensory analysis) was used. The identification of the compounds from the sniffing analysis was done with a atomic emission detector for gas chromatography. The problem stemmed from relatively volatile sulfur-organic compounds. An interesting question is if these compounds also are strongly involved in the fuel system deposit formation. This presentation shows this new analysis technique and the complex pattern of sulfur-organic compounds related to fuels from different refinery processes.

  19. Formation and stimulated photodissociation of metastable molecules with emission of photon at the collision of two atoms in a laser radiation field

    NASA Astrophysics Data System (ADS)

    Gazazyan, E.; Gazazyan, A.

    2017-04-01

    The formation of metastable molecules (Feshbach resonances) at the collision of two atoms and subsequent stimulated transition to a lower unbound electronic molecular state, with emission of a photon of the laser radiation has been investigated. This can develop, in particular, for Rb 2 molecules due to resonance scattering of two Rb atoms. This process is a basis for the creation of excimer lasers. Expressions have been obtained for the cross sections of elastic and inelastic resonance scattering and the intensity of the stimulated emission of the photons.

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

    PubMed

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

    2014-01-02

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

  1. [Study on the determination of 28 inorganic elements in sunflower seeds by ICP-OES/ICP-MS].

    PubMed

    Liu, Hong-Wei; Qin, Zong-Hui; Xie, Hua-Lin; Cao, Shu

    2013-01-01

    The present paper describes a simple method for the determination of trace elements in sunflower seeds by using inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma spectrometry (ICP-MS). HNO3 + H2O2 were used to achieve the complete decomposition of the organic matrix in a closed-vessel microwave oven. The contents of 10 trace elements (Al, B, Ca, Fe, K, Mg, Na, Si, P and S) in sunflower seeds were determined by ICP-OES while 18 trace elements (As, Ba, Cd, Co, Cr, Cu, Li, Mn, Mo, Ni, Pb, Rb, Sr, Sn, Sb, Ti, V and Zn) were determined by ICP-MS. The rice reference material (GBW10045) was used as standard reference materials. The results showed a good agreement between measured and certified values for all analytes. The concentrations of necessary micro elements Ca, K, Mg, P and S were higher. This method was simple, sensitive and precise and can perform simultaneous multi-elements determination of sunflower seeds.

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

    SciTech Connect

    Montaser, A.

    1994-09-01

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

  3. Quantum interference and radiative coupling in two-atom single-photon emission

    NASA Astrophysics Data System (ADS)

    Kurizki, G.; Ben-Reuven, A.

    1985-10-01

    The recent experiment by Grangier, Aspect, and Vigue on interference in the emission from fragments of electronically photodissociated molecules is treated as a special case of cooperative fluorescence (CF) from products of various molecular processes. This treatment relates time-resolved features of the CF to characteristics (such as orbital symmetry) of the dissociating parent molecule (PM), suggests various PM state preparations (including formation of subradiant states), and discusses the persistence of CF in systems of nonidentical fragments. The diagnostic potentialities of such studies are emphasized.

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

    SciTech Connect

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

    2004-06-30

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

  5. Angular asymmetry of low-energy electron emission in ion-atom collisions

    SciTech Connect

    Fainstein, P.D.; Gulyas, L.; Martin, F.; Salin, A.

    1996-05-01

    We show that two factors contribute to the forward-backward angular asymmetry in low-energy electron emission by ion impact: the deviation of the target potential from a pure Coulomb potential and the two-center effect. We perform calculations with various theories that include these two effects: the continuum-distorted-wave{endash}eikonal-initial-state (CDW-EIS) and the CDW approximations based on distorted-wave perturbation theory and a close-coupling calculation using a discrete representation of the continuum. The various theories give consistent results on the asymmetry but discrepancies remain between theory and experiment. {copyright} {ital 1996 The American Physical Society.}

  6. Battery-Operated Atomic Emission Analyzer for Waterborne Arsenic Based on Atmospheric Pressure Glow Discharge Excitation Source.

    PubMed

    Yang, Chun; He, Dong; Zhu, Zhenli; Peng, Huan; Liu, Zhifu; Wen, Guojun; Bai, Jianghao; Zheng, Hongtao; Hu, Shenghong; Wang, Yanxin

    2017-03-21

    In this paper, a sensitive atomic emission spectrometer (AES) based on a new low power and low argon consumption (<8 W, 100 mL min(-1)) miniature direct current (dc) atmospheric pressure glow discharge (APGD) plasma (3 mm × 5 mm) excitation source was developed for the determination of arsenic in water samples. In this method, arsenic in water was reduced to AsH3 by hydride generation (HG), which was then transported to the APGD source for excitation and detected by a compact CCD (charge-coupled device) microspectrometer. Different parameters affecting the APGD and the hydride generation reactions were investigated. The detection limit for arsenic with the proposed APGD-AES was 0.25 μg L(-1), and the calibration curves were found to be linear up to 3 orders of magnitude. The proposed method was successfully applied to the determination of certified reference material (GBW08605), tap water, pond water, groundwater, and hot spring samples. Measurements from the APGD analyzer showed good agreement with the certified value/values obtained with well-established hydride generation atomic fluorescence spectrometry (HG-AFS). These results suggest that the developed robust, cost-effective, and fast analyzer can be used for field based arsenic determination and may provide an important tool for arsenic contamination and remediation programs.

  7. Spectral and Atomic Physics Analysis of Xenon L-Shell Emission From High Energy Laser Produced Plasmas

    NASA Astrophysics Data System (ADS)

    Thorn, Daniel; Kemp, G. E.; Widmann, K.; Benjamin, R. D.; May, M. J.; Colvin, J. D.; Barrios, M. A.; Fournier, K. B.; Liedahl, D.; Moore, A. S.; Blue, B. E.

    2016-10-01

    The spectrum of the L-shell (n =2) radiation in mid to high-Z ions is useful for probing plasma conditions in the multi-keV temperature range. Xenon in particular with its L-shell radiation centered around 4.5 keV is copiously produced from plasmas with electron temperatures in the 5-10 keV range. We report on a series of time-resolved L-shell Xe spectra measured with the NIF X-ray Spectrometer (NXS) in high-energy long-pulse (>10 ns) laser produced plasmas at the National Ignition Facility. The resolving power of the NXS is sufficiently high (E/ ∂E >100) in the 4-5 keV spectral band that the emission from different charge states is observed. An analysis of the time resolved L-shell spectrum of Xe is presented along with spectral modeling by detailed radiation transport and atomic physics from the SCRAM code and comparison with predictions from HYDRA a radiation-hydrodynamics code with inline atomic-physics from CRETIN. This work was performed under the auspices of the U.S. Department of Energy by LLNL under Contract DE-AC52-07NA27344.

  8. Particle transport in a He-microchip plasma atomic emission system with an ultrasonic nebulizer for aqueous sample introduction

    NASA Astrophysics Data System (ADS)

    Oh, Joosuck; Lim, H. B.

    2008-11-01

    The transport efficiency of dried particles generated from an ultrasonic nebulizer (USN) was studied to improve the analytical performance of a lab-made, He-microchip plasma system, in which a quartz tube (~ 1 mm i.d.) was positioned inside the central channel of a poly(dimethylsiloxane) (PDMS) polymer chip. The polymer microchip plasma has the advantages of low cost, small size, easy handling and design, and self-ignition with long stabilization (> 24 h). However, direct introduction of aqueous solution into the microplasma for the detection of metals remains problematic due to plasma instability. In addition, the much smaller size of the system can cause signal suppression due to low transport efficiency. Therefore, knowledge of particle transport efficiency in this microplasma system is required to enhance the sensitivity and stability. The weight of transported particles in the range of 0.02 to 10 mg m - 3 was measured using a piezobalance with a precision of 0.4-17.8%, depending on the operating conditions. The significant effects of the USN operating conditions and the physical properties of the tubing, namely, length, inner diameter and surface characteristics, on the number of particles transported from the nebulizer to the microplasma were studied. When selected metals, such as Na, Mg and Pb, at a concentration of 5 mg L - 1 were nebulized, transported particles were obtained with a mass range of 0.5-5 mg m - 3 , depending on atomic weights. For application of the He-rf-microplasma, the atomic emission system was optimized by changing both the radio frequency (rf) power (60-200 W) and cooling temperature of the USN (- 12-9 °C). The limits of detection obtained for K, Na and Cu were 0.26, 0.22, and 0.28 mg L - 1 , respectively. These results confirmed the suitable stability and sensitivity of the He-rf-PDMS microchip plasma for application as an atomization source.

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

    NASA Astrophysics Data System (ADS)

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

    2016-06-01

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

  10. Automated system for identification of atomic elements and calculation of lines profiles in emission spectra

    NASA Astrophysics Data System (ADS)

    Ramírez, Wilder; Restrepo, Elisabeth; Devia, Alfonso

    2001-04-01

    A database was designed starting from the Kurucz cd-rom N0 23 of the Smithsonian Astrophysical Observatory. In this database the different atomic elements are ordered by wavelength with their ionization levels. Also, there are other data like statistic weight, Einstein's coefficient, information about energy levels, constant of damping, among others. The spectra of the discharge are processed using a digital filtrate technique, with the purpose of reducing the noise present in the data to locate the points where the maximum amplitudes are presented. Starting from these results, consultations dynamic SQL are made, these obtain the elements present in these regions from the database. Finally, by means of the use of statistical methods it is determined which are the elements that have the highest probability of conform with the plasma. .

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

    NASA Astrophysics Data System (ADS)

    Martínez, Filiberto; Miranda, Javier

    2013-07-01

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

  12. Observations of the O+ (2P-2D) 732 and 733 nm Thermospheric Airglow Emissions with the Wind Imaging Interferometer Leading to Atomic Oxygen Concentrations and ionospheric Winds

    NASA Astrophysics Data System (ADS)

    Shepherd, G. G.; Cho, Y. M.

    2014-12-01

    Remote sensing of airglow emission provides a powerful approach to the measurement of composition, temperature and winds in the thermosphere, on short and long time scales, including the responses to magnetic storms. Of the available emissions, one that has not been exploited to its full potential is the O+ (2P-2D) pair of doublets at 732.0 and 733.0 nm wavelength. This presentation is of recently analyzed results from WINDII, the Wind Imaging Interferometer on NASA's Upper Atmosphere Research Satellite, launched in 1991. WINDII is a Doppler Michelson interferometer with the capacity to measure airglow emission rates, Doppler temperatures from line widths and winds from Doppler shifts. One of the filters used to select specific airglow emissions was intended for measurement of the P1(2) line of the (8,3) Meinel band of OH at 731.63 nm but it also transmitted the O+ lines of interest. These have recently been retrieved from the data and are the basis of this presentation. The O+ emission is produced in the daytime, primarily from the photo-ionization of atomic oxygen and so knowing the solar flux the concentration of atomic oxygen can be determined. As a first step the variation of the emission rate on solar flux, solar zenith angle and conjugate photoelectron flux has been investigated, and preliminary results on atomic oxygen concentration are presented. In addition, ion winds can be determined from the Doppler shifts of the emission, which may be compared with the neutral winds obtained with WINDII from the atomic oxygen O(1S) and O(1D) emissions at 557.7 nm and 630.0 nm respectively. This possibility will allow the study of the interactions between the thermosphere and ionosphere for a wide range of conditions.

  13. Wafer-Size and Single-Crystal MoSe2 Atomically Thin Films Grown on GaN Substrate for Light Emission and Harvesting.

    PubMed

    Chen, Zuxin; Liu, Huiqiang; Chen, Xuechen; Chu, Guang; Chu, Sheng; Zhang, Hang

    2016-08-10

    Two-dimensional (2D) atomic-layered semiconductors are important for next-generation electronics and optoelectronics. Here, we designed the growth of an MoSe2 atomic layer on a lattice-matched GaN semiconductor substrate. The results demonstrated that the MoSe2 films were less than three atomic layers thick and were single crystalline of MoSe2 over the entire GaN substrate. The ultrathin MoSe2/GaN heterojunction diode demonstrated ∼850 nm light emission and could also be used in photovoltaic applications.

  14. Determination of volatile halogenated organic compounds in soils by purge-and-trap capillary gas chromatography with atomic emission detection.

    PubMed

    Campillo, Natalia; Viñas, Pilar; López-García, Ignacio; Aguinaga, Nerea; Hernández-Córdoba, Manuel

    2004-10-20

    Nine volatile halogenated organic compounds (VHOCs), including four trihalomethanes (THMs), were determined in soils by capillary gas chromatography with microwave induced-plasma atomic emission spectrometry (GC-AED), using a purge-and-trap system (PT) for sample preconcentration. Analytes were previously extracted from the soil sample in methanol and the extract was preconcentrated before being chromatographed. Element-specific detection and quantification were carried out monitoring two wavelength emission lines, corresponding to chlorine (479nm) and bromine (478nm). Each chromatographic run took 21min, including the purge step. The method showed a precision of 1.1-7.2% (R.S.D.) depending on the compound. Detection limits ranged from 0.05 to 0.55ngml(-1), for chloroform and dichloromethane, respectively, corresponding to 3.3 and 36.0ngg(-1) in the soil samples. The chromatographic profiles obtained showed no interference from co-extracted compounds. Low levels of dichloromethane and chloroform ranging from 0.04 to 1.13mugg(-1) were found in samples obtained from small gardens irrigated with tap water. The method is reliable and can be used for routine monitoring in soil samples.

  15. Chemical vapor generation for sample introduction into inductively coupled plasma atomic emission spectroscopy: vaporization of antimony(III) with bromide.

    PubMed

    Lopez-Molinero, A; Mendoza, O; Callizo, A; Chamorro, P; Castillo, J R

    2002-10-01

    A new method for antimony determination in soils is proposed. It is based on the chemical vapor generation of Sb(III) with bromide, after a reaction in sulfuric acid media and transport of the gaseous phase into an inductively coupled plasma for atomic emission spectrometry. The experimental variables influencing the method were delimited by experimental design and the most important were finally optimized by the modified Simplex method. In optimized conditions the method involves the reaction of 579 microl concentrated sulfuric acid with 120 microl 5% w/v KBr and 250 microl antimony solution. Measurement of antimony emission intensity at 217.581 nm provides a method with an absolute detection limit of 3.5 ng and a precision (RSD) of 5.8% for the injection of five replicates of 175 ng Sb(III) (250 microl of 0.7 microg ml(-1) solution). The interference of common anions and cations on the antimony signal was evaluated. A 21% Sb(III) volatilization efficiency was calculated from the mean of six experiments at optimum conditions. The accuracy of the methodology was checked by the analysis of one standard reference soil after acid decomposition heating in a microwave oven.

  16. The interaction of 193-nm excimer laser radiation with single-crystal zinc oxide: The generation of atomic Zn line emission at laser fluences below breakdown

    SciTech Connect

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

    2013-08-22

    The production of gas phase atomic and ionic line spectra accompanying the high laser fluence irradiation of solid surfaces is well known and is most often due to the production and interaction of high densities of atoms, ions, and electrons generated from laser-induced breakdown. The resulting plasma expands and moves rapidly away from the irradiated spot and is accompanied by intense emission of light. This type of plume is well studied and is frequently exploited in the technique of chemical analysis known as laser induced breakdown spectroscopy. Here, we describe a similar but weaker emission of light generated in vacuum by the laser irradiation of single crystal ZnO at fluences well below breakdown; this emission consists entirely of optical line emission from excited atomic Zn. Furthermore, we compare the properties of the resulting laser-generated gas-phase light emission (above and below breakdown) and describe a mechanism for the production of the low-fluence optical emission resulting from a fortuitous choice of material and laser wavelength.

  17. The interaction of 193-nm excimer laser radiation with single-crystal zinc oxide: The generation of atomic Zn line emission at laser fluences below breakdown

    SciTech Connect

    Khan, Enamul H.; Langford, S. C.; Dickinson, J. T.; Boatner, L. A.

    2013-08-28

    The production of gas phase atomic and ionic line spectra accompanying the high laser fluence irradiation of solid surfaces is well known and is most often due to the production and interaction of high densities of atoms, ions, and electrons generated from laser-induced breakdown. The resulting plasma expands and moves rapidly away from the irradiated spot and is accompanied by intense emission of light. This type of “plume” is well studied and is frequently exploited in the technique of chemical analysis known as laser induced breakdown spectroscopy. Here, we describe a similar but weaker emission of light generated in vacuum by the laser irradiation of single crystal ZnO at fluences well below breakdown; this emission consists entirely of optical line emission from excited atomic Zn. We compare the properties of the resulting laser-generated gas-phase light emission (above and below breakdown) and describe a mechanism for the production of the low-fluence optical emission resulting from a fortuitous choice of material and laser wavelength.

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

    SciTech Connect

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

    1995-08-01

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

  19. Observations of argon emission lines used for fluorine atom actinometry in low power rf discharges

    NASA Astrophysics Data System (ADS)

    Savas, S. E.

    1986-04-01

    Anomalous power and frequency dependences of some argon emission lines are observed in a low power rf discharge in a 2% admixture of argon in CF4. Frequency ranges from 0.12 to 13.56 MHz for pressures of 25 and 50 mTorr and 20 W power to the plasma. Power and frequency dependences of the 7504 Å line differ from those for the 6416 Å, 6871 Å, and 7126 Å lines. These differences and argon excitation cross sections are used to examine the validity of actinometry assumptions. The 6871 Å or 6416 Å lines work better under these conditions as actinometer references, while the 7504 Å seems preferable for etch plasmas.

  20. Distribution profiles of sulphur in caramel colours on a gel-filtration column studied by HPLC/ICP.

    PubMed

    Maitani, T; Kubota, H; Yamada, T

    1996-01-01

    The distribution profiles of sulphur in commercial caramel colours I, III and IV on a gel-filtration column were studied with a high performance liquid chromatograph (HPLC) connected directly to a vacuum-ultraviolet inductively coupled plasma-atomic emission spectrometer (ICP). A small sulphur peak of sulphate was detected in most products of caramel III, whereas caramel I products did not exhibit a sulphur peak, as predicted from the total sulphur concentration. In caramel IV products, sulphur was detected continuously in the fractions of the colouring ingredients with high molecular weights. The molar ratio of sulphur was bound to every 2-4 molecules of original hexose. However, sulphur was also contained in lower molecular weight fractions which were not the colouring constituents, the content being over twice that of the colouring ingredients.

  1. Determination of trace impurities in high-purity zirconium dioxide by inductively coupled plasma atomic emission spectrometry using microwave-assisted digestion and wavelet transform-based correction procedure.

    PubMed

    Ma, Xiaoguo; Li, Yibing

    2006-10-02

    This paper describes a rapid, accurate and precise method for the determination of trace Fe, Hf, Mn, Na, Si and Ti in high-purity zirconium dioxide (ZrO2) powders by inductively coupled plasma atomic emission spectrometry (ICP-AES). The samples were dissolved by a microwave-assisted digestion system. Four different digestion programs with various reagents were tested. It was found that using a mixture of sulfuric acid (H2SO4) and ammonium sulfate ((NH4)2SO4), the total sample dissolution time was 30 min, much shorter than that required for conventional digestion in an opening system. The determination of almost all of the target analytes suffered from spectral interferences, since Zr shows a line-rich atomic emission spectrometry. The wavelet transform (WT), a recently developed mathematical technique was applied to the correction of spectral interference, and more accurate and precise results were obtained, compared with traditional off-peak background correction procedure. Experimental work revealed that a high Zr concentration would result in a significant decrease in peak height of the analyte lines, which was corrected by standard addition method. The performance of the developed method was evaluated by using synthetic samples. The recoveries were in the range of 87-112% and relative standard deviation was within 1.1-3.4%. The detection limits (3sigma) for Fe, Hf, Mn, Na, Si and Ti were found to be 1.2, 13.3, 1.0, 4.5, 5.8 and 2.0 microg g(-1), respectively. The results showed that with the microwave-assisted digestion and the WT correction, the detection limits have improved by a factor of about 5 for Fe, 4 for Mn and Ti, 3 for Si, and 2 for Hf and Na, respectively, in comparison with conventional open-system digestion and off-peak correction. The proposed technique was applied to the analysis of trace elements above-mentioned in three types of ZrO2 powders.

  2. Direct determination of cadmium in solids using a capacitively coupled microwave plasma atomic emission spectrometer.

    PubMed

    Pless, A M; Croslyn, A; Gordon, M J; Smith, B W; Winefordner, J D

    1997-01-01

    A capacitively coupled microwave plasma (CMP) operating at 800 W was examined for the direct determination of cadmium in solids. The laboratory-constructed system contained a tungsten cup electrode capable of holding microsample quantities. A low-powered plasma was used to heat the sample, while at higher powers the plasma was used for sample vaporization and excitation. This plasma enabled thermal vaporization (TV) sample introduction to be accomplished in situ as the plasma formed directly around the sample. Thus, the need for sample preparation, procedural steps and sample transport was eliminated. This technique was capable of the direct determination of trace elements in solid samples in less than 5 min. The effects of experimental parameters such as gas flow rate, atomization power and electrode position were investigated. Detection limits obtained for Cd by TV-CMP-AES were in the picogram range with a relative standard deviation of <20%. The accuracy and precision of the method were also evaluated by measuring Cd in several NIST Standard Reference Materials.

  3. Determination of Vanadium, Tin and Mercury in Atmospheric Particulate Matter and Cement Dust Samples by Direct Current Plasma Atomic Emission Spectrometry.

    ERIC Educational Resources Information Center

    Hindy, Kamal T.; And Others

    1992-01-01

    An atmospheric pollution study applies direct current plasma atomic emission spectrometry (DCP-AES) to samples of total suspended particulate matter collected in two industrial areas and one residential area, and cement dust collected near major cement factories. These samples were analyzed for vanadium, tin, and mercury. The results indicate the…

  4. Determination of Vanadium, Tin and Mercury in Atmospheric Particulate Matter and Cement Dust Samples by Direct Current Plasma Atomic Emission Spectrometry.

    ERIC Educational Resources Information Center

    Hindy, Kamal T.; And Others

    1992-01-01

    An atmospheric pollution study applies direct current plasma atomic emission spectrometry (DCP-AES) to samples of total suspended particulate matter collected in two industrial areas and one residential area, and cement dust collected near major cement factories. These samples were analyzed for vanadium, tin, and mercury. The results indicate the…

  5. Measuring atomic emission from beacons for long-distance chemical signaling.

    PubMed

    LaFratta, Christopher N; Pelse, Ian; Falla, Jose Luis; Liu, Yi; Palacios, Manuel A; Manesse, Mael; Whitesides, George M; Walt, David R

    2013-10-01

    In an effort to exploit chemistry for information science, we have constructed a system to send a message powered by a combustion reaction. Our system uses the thermal excitation of alkali metals to transmit an encoded signal over long distances. A message is transmitted by burning a methanol-soaked cotton string embedded with combinations of high, low, or zero levels of potassium, rubidium, and/or cesium ions. By measuring the intensities at the characteristic emission wavelengths of each metal in the near-infrared, 19 unique signals can be distinguished. We have built a custom telescope to detect these signals from 1 km away for nearly 10 min. The signal is isotropic, is self-powered, and has a low background. A potential application of this platform is for search and rescue signaling where another layer of information can be transmitted, in addition to the location of the beacon. This work, which seeks to encode and transmit information using chemistry instead of electronics, is part of the new field of "infochemistry".

  6. Atomic Emission, Absorption and Fluorescence in the Laser-induced Plasma

    SciTech Connect

    Winefordner, J. D.

    2009-01-22

    The main result of our efforts is the development and successful application of the theoretical model of laser induced plasma (LIP) that allows a back-calculation of the composition of the plasma (and the condensed phase) based on the observable plasma spectrum. The model has an immediate experimental input in the form of LIP spectra and a few other experimentally determined parameters. The model is also sufficiently simple and, therefore, practical. It is conveniently interfaced in a graphical user-friendly form for using by students and any laboratory personnel with only minimal training. In our view, the model opens up the possibility for absolute analysis, i.e. the analysis which requires no standards and tedious calibration. The other parts of this proposal (including plasma diagnostics) were somewhat subordinate to this main goal. Plasma diagnostics provided the model with the necessary experimental input and led to better understanding of plasma processes. Another fruitful direction we pursued was the use of the correlation analysis for material identification and plasma diagnostics. Through a number of computer simulations we achieved a clear understanding of how, where and why this approach works being applied to emission spectra from a laser plasma. This understanding will certainly improve the quality of forensic and industrial analyses where fast and reliable material identification and sorting are required.

  7. Focused microwave-induced combustion for digestion of botanical samples and metals determination by ICP OES and ICP-MS.

    PubMed

    Barin, J S; Pereira, J S F; Mello, P A; Knorr, C L; Moraes, D P; Mesko, M F; Nóbrega, J A; Korn, M G A; Flores, E M M

    2012-05-30

    The advantages and shortcomings of focused microwave-induced combustion (FMIC) for digestion of plant samples were studied. The effects of sample mass, absorbing solution, oxygen gas flow-rate, and time of reflux step on recoveries of major, minor and trace metals were systematically evaluated. Afterwards, Al, Ba, Ca, Co, Cr, Cu, Mg, Mn, Ni, Sr, V, and Zn were determined by inductively coupled plasma optical emission spectrometry (ICP OES) and by inductively coupled plasma mass spectrometry (ICP-MS). The main advantages of FMIC when compared to microwave-assisted wet digestion (MAWD) and focused-microwave-assisted wet digestion (FMAWD) are the possibility to digest larger masses of samples (up to 3g) using shorter heating times and diluted nitric acid solution for absorbing all analytes. Using the selected experimental conditions for FMIC, residual carbon content was lower than 0.7% for all samples and relative standard deviation (RSD) varied from 1.5 to 14.1%. Certified reference materials (NIST 1515 apple leaves and NIST 1547 peach leaves) were used for checking accuracy and determined values for all metals were in agreement with certified values at a 95% confidence level. No statistical difference (ANOVA, 95% of confidence level) was observed for results obtained by FMIC, FMAWD, and MAWD. Limits of detection were lower when using FMIC in the range of 0.02-0.15 μg g(-1) for ICP OES and 0.001-0.01 μg g(-1) for ICP-MS, which were about 3 and 6 times lower than the values obtained by FMAWD and MAWD, respectively. It is important to point out that FMIC was a suitable sample preparation method for major, minor and trace metals by both determination techniques (ICP OES and ICP-MS). Additionally, since it allows lower LODs (because up to 3g of sample can be digested) and diluted acid solutions are used (without any further dilution), the use of ICP-MS is not mandatory.

  8. Evaluation of an improved atomic data basis for carbon in UEDGE emission modeling for L-mode plasmas in DIII-D

    NASA Astrophysics Data System (ADS)

    Muñoz Burgos, J. M.; Leonard, A. W.; Loch, S. D.; Ballance, C. P.

    2013-07-01

    New scaled carbon atomic electron-impact excitation data is utilized to evaluate comparisons between experimental measurements and fluid emission modeling of detached plasmas at DIII-D. The C I and C II modeled emission lines for 909.8 and 514.7 nm were overestimated by a factor of 10-20 than observed experimentally for the inner leg, while the outer leg was within a factor of 2. Due to higher modeled emissions, a previous study using the UEDGE code predicted that a higher amount of carbon was required to achieve a detached outboard divertor plasma in L-mode at DIII-D. The line emission predicted by using the new scaled carbon data yields closer results when compared against experiment. We also compare modeling and measurements of Dα emission from neutral deuterium against predictions from newly calculated R-Matrix with pseudostates data available at the ADAS database.

  9. The delayed ionization and atomic ion emission of binary metal metallocarbohedrenes TixMyC12 (M=Zr, Nb; 0 <= y <= 4; x+y=8)

    NASA Astrophysics Data System (ADS)

    Cartier, S. F.; May, B. D.; Castleman, A. W., Jr.

    1996-03-01

    Investigations of the photophysical character of binary metal containing metallocarbohedrene clusters (Met-Cars), reveal the phenomena of delayed ionization. Additionally, the onset of a channel corresponding to delayed atomic ion emission is observed at high laser fluence, becoming progressively more significant as the fluence is raised. The fluence dependence of both the delayed electron and delayed atomic ion emission channels at 355 and 532 nm are reported, and the Met-Car delayed ion yield estimated. At moderate fluences, the yield of the delayed electron emission channel leading to the Met-Car ion is found to be on the order of 70% of the total Met-Car signal. All of the experimental findings point to thermionic emission being the operative mechanism for the delayed ionization, while the delayed atomic ion emission is evidently a new mechanism [B. D. May, S. F. Cartier, and A. W. Castleman, Jr., Chem. Phys. Lett. 242, 265 (1995)] which may be due to the collective electronic excitation of these cluster materials.

  10. Emission Characteristics of Ca and Mg Atoms in Gas Plasma Induced by the Bombardment of Transversely Excited Atmospheric CO2 Laser at 1 atm

    NASA Astrophysics Data System (ADS)

    Khumaeni, Ali; Sukra Lie, Zener; Inn Lee, Yong; Kurihara, Kazuyoshi; Hendrik Kurniawan, Koo; Fukumoto, Ken-ichi; Kagawa, Kiichiro; Niki, Hideaki

    2012-08-01

    To study the mechanism of atomic excitation in gas plasma, a transversely excited atmospheric pressure (TEA) CO2 laser (750 mJ, 200 ns) was focused on a metal subtarget through a hole (2 mm in diameter) produced in a glass slide sample (1.5 mm in thickness); the glass slide sample was placed in close contact with a nickel metal plate, which functions as the metal subtarget. It was demonstrated that a strong gas plasma can be induced in various gases including He, N2, and CO2 and that plasma can be employed as the excitation source for spectrochemical analysis. It has been proved that, in He gas plasma, strong Ca ionic emissions (Ca II 393.3 nm and Ca II 373.7 nm) with a long lifetime can be observed regardless of excitation energy. On the other hand, in N2 and CO2 gases, the emissions are very weak and have a short lifetime. We assumed that, in He gas plasma, He metastable atoms play significant role in excitation. In the case of the Ca atom, the double ionization of Ca (Ca2+) is directly induced when a Ca atom collides with He metastable atoms through the Penning effect. The ion produced then recombines with an electron to produce an ionic excitation state, from which ionic emission is induced. In neutral Ca and Mg emissions, unique emission characteristics were observed in the He gas plasma case, namely, the triplet state is the main product and the singlet state is a minor product. This result can be explained by our proposed model.

  11. Qualitative tissue differentiation by analysing the intensity ratios of atomic emission lines using laser induced breakdown spectroscopy (LIBS): prospects for a feedback mechanism for surgical laser systems.

    PubMed

    Kanawade, Rajesh; Mahari, Fanuel; Klämpfl, Florian; Rohde, Maximilian; Knipfer, Christian; Tangermann-Gerk, Katja; Adler, Werner; Schmidt, Michael; Stelzle, Florian

    2015-01-01

    The research work presented in this paper focuses on qualitative tissue differentiation by monitoring the intensity ratios of atomic emissions using 'Laser Induced Breakdown Spectroscopy' (LIBS) on the plasma plume created during laser tissue ablation. The background of this study is to establish a real time feedback control mechanism for clinical laser surgery systems during the laser ablation process. Ex-vivo domestic pig tissue samples (muscle, fat, nerve and skin) were used in this experiment. Atomic emission intensity ratios were analyzed to find a characteristic spectral line for each tissue. The results showed characteristic elemental emission intensity ratios for the respective tissues. The spectral lines and intensity ratios of these specific elements varied among the different tissue types. The main goal of this study is to qualitatively and precisely identify different tissue types for tissue specific laser surgery. © 2015 The Authors. Journal of Biophotonics published by WILEY-VCH Verlag.

  12. Multielemental analysis of purpleback flying squad using high resolution inductively coupled plasma-mass spectrometry (HR ICP-MS).

    PubMed

    Ichihashi, H; Kohno, H; Kannan, K; Tsumura, A; Yamasaki, S I

    2001-08-01

    Forty-four elements were analyzed in 21 tissues of purpleback flying squid, Sthenoteuthis oualaniensis, by high resolution inductively coupled plasma-mass spectrometry (HR ICP-MS) and inductively coupled plasma atomic emission spectrophotometry (ICP-AES). Greater concentrations of V, Fe, Co, Ni, Cu, Ag, Cd, Pb, and Bi were found in liver, pancreas, and ink sac than in other tissues. Ink sac concentrated remarkable levels of Ca and Sr in addition to the above-mentioned elements. Several alkalis, alkaline earth, and rare earth elements preferentially accumulated in muscle. Among the hard tissues, accumulation of V and U in beak, Ni, Zn, and Cd in gladius and Cr in skin was prominent. K, Rb, Cs, Pb, Bi and some transition elements (V, Co, Cu, Zn, Ag, Cd) were significantly (p < 0.05) higher in the livers of adult than in juvenile squids. Sodium, alkaline earth, and rare earth elements were higher in the livers of juveniles than in adult squids.

  13. ICP27-dependent resistance of herpes simplex virus type 1 to leptomycin B is associated with enhanced nuclear localization of ICP4 and ICP0

    SciTech Connect

    Lengyel, Joy; Strain, Anna K.; Perkins, Keith D.; Rice, Stephen A. . E-mail: ricex019@umn.edu

    2006-09-01

    It was previously shown that herpes simplex virus type 1 (HSV-1) is sensitive to leptomycin B (LMB), an inhibitor of nuclear export factor CRM1, and that a single methionine to threonine change at residue 50 (M50T) of viral immediate-early (IE) protein ICP27 can confer LMB resistance. In this work, we show that deletion of residues 21-63 from ICP27 can also confer LMB resistance. We further show that neither the M50T mutation nor the presence of LMB affects the nuclear shuttling activity of ICP27, suggesting that another function of ICP27 determines LMB resistance. A possible clue to this function emerged when it was discovered that LMB treatment of HSV-1-infected cells dramatically enhances the cytoplasmic accumulation of two other IE proteins, ICP0 and ICP4. This effect is completely dependent on ICP27 and is reversed in cells infected with LMB-resistant mutants. Moreover, LMB-resistant mutations in ICP27 enhance the nuclear localization of ICP0 and ICP4 even in the absence of LMB, and this effect can be discerned in transfected cells. Thus, the same amino (N)-terminal region of ICP27 that determines sensitivity to LMB also enhances ICP27's previously documented ability to promote the cytoplasmic accumulation of ICP4 and ICP0. We speculate that ICP27's effects on ICP4 and ICP0 may contribute to HSV-1 LMB sensitivity.

  14. Determination of selected elements in whole coal and in coal ash from the eight argonne premium coal samples by atomic absorption spectrometry, atomic emission spectrometry, and ion-selective electrode

    USGS Publications Warehouse

    Doughten, M.W.; Gillison, J.R.

    1990-01-01

    Methods for the determination of 24 elements in whole coal and coal ash by inductively coupled argon plasma-atomic emission spectrometry, flame, graphite furnace, and cold vapor atomic absorption spectrometry, and by ion-selective electrode are described. Coal ashes were analyzed in triplicate to determine the precision of the methods. Results of the analyses of NBS Standard Reference Materials 1633, 1633a, 1632a, and 1635 are reported. Accuracy of the methods is determined by comparison of the analysis of standard reference materials to their certified values as well as other values in the literature.

  15. Determination of tungsten in niobium-tantalum, vanadium and molybdenum bearing geological samples using derivative spectrophotometry and ICP-AES.

    PubMed

    Padmasubashini, V; Ganguly, M K; Satyanarayana, K; Malhotra, R K

    1999-10-01

    Two different procedures, one using derivative spectrophotometry and another using inductively coupled plasma atomic emission spectrometry (ICP-AES) have been developed for the determination of tungsten in niobate-tantalates, tin slag samples, ores, concentrates and vanadium and molybdenum bearing geological materials. In the first method involving derivative spectrophotometry, 0.05-0.5 g of the sample is fused with sodium hydroxide, the tungsten is extracted by leaching the melt with distilled water and estimated as thiocyanate using a second derivative spectrophotometric method in the presence of interferents, i.e. Nb, Mo and V, without separating them. Mixtures of tungsten with V, Nb and Mo are used for standardizing the various parameters like zero-crossing wavelength, wavelength range, etc. Tolerance limits for V, Nb and Mo have also been evaluated. In the second method involving ICP-AES, 0.05-0.5 g of sample is fused with KHSO(4) to a clear melt and dissolved in ammonium oxalate solution. Ammonium hydroxide precipitation is then carried out to separate Nb and Ta as hydroxides and the filtrate is boiled with nitric acid to destroy the oxalates before aspiration into the plasma for measurement of tungsten values by ICP-AES using the 207.911 nm emission line. Both methods have been applied to niobate-tantalate and tin slag samples and the results obtained are reported in this paper. The values obtained by both methods are in good agreement with each other. The proposed methods have also been applied to the determination of tungsten in two Canadian Certified Reference Standards (CT-1 and MP-2) and the values obtained are in good agreement with the certified values and the R.S.D.% in case of the ICP-AES method varied from 1-2% at >1000 mug g(-1) level to 9.4% at the 20 mug g(-1) level whereas the R.S.D.% in case of the derivative method varied from 1 to 7.8%.

  16. Teacher Reaction to ICP Quality Assurance Procedures.

    ERIC Educational Resources Information Center

    Leonard, Ann

    An integral part of the Quality Assurance Manual developed by Southwest Regional Laboratory (SWRL) to accompany the Kindergarten Program is the end-of-program assessment of the Instructional Concepts Program (ICP). Following completion of ICP Quality Assurance assessment, four teachers were interviewed in order to gather information pertinent to…

  17. Individualized Career Plan (ICP): Implementation Manual.

    ERIC Educational Resources Information Center

    Batsche, Catherine; And Others

    This implementation manual was designed to assist local education agency personnel implement the individualized career plan (ICP) concept in high schools. Questions commonly asked about the ICP are answered. Guidelines are then provided for implementing the four stages of the process: planning, developing, implementing, and evaluating/refining.…

  18. The use of atomic spectroscopy in the pharmaceutical industry for the determination of trace elements in pharmaceuticals.

    PubMed

    Lewen, Nancy

    2011-06-25

    The subject of the analysis of various elements, including metals and metalloids, in the pharmaceutical industry has seen increasing importance in the last 10-15 years, as modern analytical instrumentation has afforded analysts with the opportunity to provide element-specific, accurate and meaningful information related to pharmaceutical products. Armed with toxicological data, compendial and regulatory agencies have revisited traditional approaches to the testing of pharmaceuticals for metals and metalloids, and analysts have begun to employ the techniques of atomic spectroscopy, such as flame- and graphite furnace atomic absorption spectroscopy (FAAS, Flame AA or FAA and GFAAS), inductively coupled plasma-atomic emission spectroscopy (ICP-AES) and inductively coupled plasma-mass spectrometry (ICP-MS), to meet their analytical needs. Newer techniques, such as laser-induced breakdown spectroscopy (LIBS) and Laser Ablation ICP-MS (LAICP-MS) are also beginning to see wider applications in the analysis of elements in the pharmaceutical industry.This article will provide a perspective regarding the various applications of atomic spectroscopy in the analysis of metals and metalloids in drug products, active pharmaceutical ingredients (API's), raw materials and intermediates. The application of atomic spectroscopy in the analysis of metals and metalloids in clinical samples, nutraceutical, metabolism and pharmacokinetic samples will not be addressed in this work.

  19. Resonant laser ablation of metals detected by atomic emission in a microwave plasma and by inductively coupled plasma mass spectrometry.

    PubMed

    Cleveland, Danielle; Stchur, Peter; Hou, Xiandeng; Yang, Karl X; Zhou, Jack; Michel, Robert G

    2005-12-01

    It has been shown that an increase in sensitivity and selectivity of detection of an analyte can be achieved by tuning the ablation laser wavelength to match that of a resonant gas-phase transition of that analyte. This has been termed resonant laser ablation (RLA). For a pulsed tunable nanosecond laser, the data presented here illustrate the resonant enhancement effect in pure copper and aluminum samples, chromium oxide thin films, and for trace molybdenum in stainless steel samples, and indicate two main characteristics of the RLA phenomenon. The first is that there is an increase in the number of atoms ablated from the surface. The second is that the bandwidth of the wavelength dependence of the ablation is on the order of 1 nm. The effect was found to be virtually identical whether the atoms were detected by use of a microwave-induced plasma with atomic emission detection, by an inductively coupled plasma with mass spectrometric detection, or by observation of the number of laser pulses required to penetrate through thin films. The data indicate that a distinct ablation laser wavelength dependence exists, probably initiated via resonant radiation trapping, and accompanied by collisional broadening. Desorption contributions through radiation trapping are substantiated by changes in crater morphology as a function of wavelength and by the relatively broad linewidth of the ablation laser wavelength scans, compared to gas-phase excitation spectra. Also, other experiments with thin films demonstrate the existence of a distinct laser-material interaction and suggest that a combination of desorption induced by electronic transition (DIET) with resonant radiation trapping could assist in the enhancement of desorption yields. These results were obtained by a detailed inspection of the effect of the wavelength of the ablation laser over a narrow range of energy densities that lie between the threshold of laser-induced desorption of species and the usual analytical

  20. The molecular oxygen dayglow emissions as proxies for atomic oxygen and ozone in the mesosphere and lower thermosphere.

    NASA Astrophysics Data System (ADS)

    Yankovsky, Valentine A.; Manuilova, Rada; Martyshenko, Kseniia

    Currently there is no reliable method for remote sensing of altitude profile of the [O( (3) P)] in the daytime mesosphere and lower thermosphere, but atomic oxygen is a key component in the mechanism of the atmosphere cooling by quenching of vibrationally excited CO _{2} molecules and also one of basic quencher of electronically excited components in MLT region. On the other hand, airglow emission in 1.27 mum IR Atm(0 - 0) band from O _{2}(a (1) Delta _{g}, v = 0) has been used as a proxy for [O _{3}] in MLT for over a decade. However, this method is not suitable for detecting of relatively rapid [O _{3}] variations which occur due to the variability of the solar spectrum in the UV range (120 - 320 nm) and other space factors. The reason of above mentioned is the large value of photochemical lifetime of the O _{2}(a (1) Delta _{g}, v = 0) molecule which is within tau _{O2(a)} =3 (.) 10 (2) - 1 (.) 10 (3) s in the mesosphere and reaches 3 (.) 10 (3) s in the lower thermosphere. The aim of this study is revealing of proxies for retrievals of [O( (3) P)] and [O _{3}]. In the framework of developed model of electronic vibrational kinetics of excited products of O _{3} and O _{2} photolysis in MLT of the Earth (model YM-2011) [1] we solved direct problem for the system of 10 kinetic equations for populations of electronically-vibrationally excited levels of oxygen molecule O _{2}(a (1) Delta _{g}, v=0 - 5), O _{2}(b (1) Sigma (+) _{g}, v=0, 1, 2) and excited oxygen atom O( (1) D). In whole, more than 60 aeronomical reactions of photoexcitation and deexcitation, of energy transfer between these excited levels and of quenching of the levels in collisions with O( (3) P), O _{2}, N _{2}, O _{3} and CO _{2} are considered. Sensitivity analysis of obtained solutions showed that emissions in 629 nm band of the O _{2}(b (1) Sigma (+) _{g}, v=2) and 762 nm band of the O _{2}(b (1) Sigma (+) _{g}, v=0) molecules can be effective proxies for atomic oxygen in the altitude range 85

  1. Development of transient data acquisition system for hyphenated techniques coupled with inductively coupled plasma atomic emission spectrometry

    NASA Astrophysics Data System (ADS)

    Wang, Xiaoru; Zhuang, Zhixia; Yang, Chenglong; Yang, Pengyuan; Yan, Xiaomei; Lin, Jianming

    1996-12-01

    A transient data acquisition system for flow injection analysis (FIA), high performance liquid chromatography (HPLC), and electrothermal vaporization (ETV) combined with ICP-AES multi-element instrumentation was developed and successfully applied to the analysis of different types of samples, including human serum, human hair and tea, for simultaneous multi-element determinations. The accuracy of the method was verified with hair reference material. Good agreement between the experimental results and certified values, and also satisfactory recoveries from standard additions, were achleved.

  2. Comparison of simultaneous continuous intracranial pressure (ICP) signals from a Codman and a Camino ICP sensor.

    PubMed

    Eide, Per Kristian

    2006-07-01

    Simultaneous continuous intracranial pressure (ICP) signals from two different sensors were compared. Continuous ICP monitoring from two ICP sensors (i.e. Codman ICP MicroSensor; Johnson & Johnson, Raynham, MA and Camino OLM ICP; Camino Laboratories, San Diego, CA) placed within the brain parenchyma was performed in three patients within the intensive care unit (ICU) as part of routine management of severe subarachnoid hemorrhage. For each 6s time window mean ICP was computed, showing large differences in mean ICP values between the signals. Differences above 5 mmHg were observed in 13% of the 128,425 time windows derived from 214 h ICP recordings in these three patients. In one patient, mean ICP differed more than 10 mmHg in 23% of the time windows. Comparisons of 675,503 individual single pressure wave pairs of these 128,425 time windows revealed marginal differences in single wave amplitude (dP, i.e. pulse pressure) and latency (dT, i.e. rise time) values, suggesting that differences in mean ICP were caused by differences in baseline pressure. For the individual time windows were computed the mean wave amplitude and mean wave latency values according to a new algorithm. There were as well marginal differences between signals of mean wave amplitude and latency values. Thus, changes in baseline pressure affect mean ICP but not single pressure wave characteristics such as amplitude (dP) and (dT) latency values.

  3. Candidate reference measurement procedures for chloride, potassium, sodium, calcium, magnesium, and lithium by inductively coupled plasma (isotope dilution) sector field mass spectrometry (ICP-(ID) SFMS) in serum.

    PubMed

    Kramer, U; Kress, M; Reinauer, H; Spannagl, M; Kaiser, P

    2013-01-01

    Standardization of the measurement of electrolyte concentrations in serum is of considerable interest for quality assurance in patient care. To promote the ongoing process of standardization we developed candidate reference measurement procedures of highest metrological order for Cl, K, Na, Ca, Mg, and Li using ICP-(ID) SFMS. Serum samples were diluted with 4 mmol/L nitric acid and were spiked with the internal standard for quantification, separately for each analyte. The samples were introduced in the ICP-SFMS device by continuous infusion using a peristaltic pump. The measurement results were compared with reference measurement procedure values obtained by atom absorption spectroscopy, flame emission spectroscopy, and coulometry. The measurement accuracy and precision was calculated by analyzing certified reference materials and EQAS samples. The mean coefficient of variation (CV) of the ICP-MS procedures for the serum samples was 0.65% for Cl, 0.46% for K, 0.51% for Na, 0.77% for Ca, 0.78% for Mg, and 0.58% for Li. The mean bias from target values of NIST certified reference materials was +0.85% for Cl, -0.46% for K, +0.68% for Na, -0.21% for Ca, +0.27% for Mg, and -0.39% for Li. Candidate reference measurement procedures for 6 electrolytes were developed by high performance magnetic sector field ICP-MS fulfilling the requirements of ISO 15193:2009 for reference measurement procedures with traceability to SI according to ISO 17511:2003 and can be used for setting target values in EQAS and for certification of reference materials.

  4. Optical emission spectroscopy of metal-halide lamps: Radially resolved atomic state distribution functions of Dy and Hg

    NASA Astrophysics Data System (ADS)

    Nimalasuriya, T.; Flikweert, A. J.; Stoffels, W. W.; Haverlag, M.; van der Mullen, J. J. A. M.; Pupat, N. B. M.

    2006-03-01

    Absolute line intensity measurements are performed on a metal-halide lamp. Several transitions of atomic and ionic Dy and atomic Hg are measured at different radial positions from which we obtain absolute atomic and ionic Dy intensity profiles. From these profiles we construct the radially resolved atomic state distribution function (ASDF) of the atomic and ionic Dy and the atomic Hg. From these ASDFs several quantities are determined as functions of radial position, such as the (excitation) temperature, the ion ratio Hg+/Dy+, the electron density, the ground state, and the total density of Dy atoms and ions. Moreover, these ASDFs give us insight about the departure from equilibrium. The measurements show a hollow density profile for the atoms and the ionization of atoms in the center. In the outer parts of the lamp molecules dominate.

  5. Optical emission spectroscopy of metal-halide lamps: Radially resolved atomic state distribution functions of Dy and Hg

    SciTech Connect

    Nimalasuriya, T.; Flikweert, A.J.; Stoffels, W.W.; Haverlag, M.; Mullen, J.J.A.M. van der; Pupat, N.B.M.

    2006-03-01

    Absolute line intensity measurements are performed on a metal-halide lamp. Several transitions of atomic and ionic Dy and atomic Hg are measured at different radial positions from which we obtain absolute atomic and ionic Dy intensity profiles. From these profiles we construct the radially resolved atomic state distribution function (ASDF) of the atomic and ionic Dy and the atomic Hg. From these ASDFs several quantities are determined as functions of radial position, such as the (excitation) temperature, the ion ratio Hg{sup +}/Dy{sup +}, the electron density, the ground state, and the total density of Dy atoms and ions. Moreover, these ASDFs give us insight about the departure from equilibrium. The measurements show a hollow density profile for the atoms and the ionization of atoms in the center. In the outer parts of the lamp molecules dominate.

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

    PubMed

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

    2011-10-15

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

  7. [Characterization of dinosaur fossils and their surrounding rocks by atomic emission spectrometry and X-ray powder diffractometry].

    PubMed

    Yang, Qun; Wang, Yi-lin; Li, Chao-zhen; Yuan, Bo

    2005-02-01

    More dinosaur fossils have been found in the Laochangqing valley, Lufeng county than anywhere else in the world, and the dinosaur fossils found here cover the longest time span (including the early and middle Jurassic ages). This excavation offers an ideal experimental base for prehistoric biology studies. This paper presents an elementary analysis of the components and structure of the dinosaur fossils in three different geologic-layers and their surrounding rocks in the above mentioned area. Atomic emission spectrum shows that the fossils are rich in the contents of calcium (>5%) and phosphor, but low in the content of silicon (3%-8%), while the surrounding rocks are high in the content of silicon (>10%). Furthermore, XRD results show that the major compound of the fossils is CaCO3 (66%), followed by SiO2 (17%); while that of the surrounding rocks is SiO2 (>80%), followed by CaCO3 (<12%). The most important difference between the fossils and the surrounding rocks is, according to the experiment, that phosphate has been identified in the former but not in the latter. This is a characteristic that can be used to distinguish the dinosaur fossils from other rocks. This paper provides valuable data for further zoological studies on the living conditions and evolution of the dinosaurs in the Laochangqing valley, Lufeng county.

  8. Microplasma source based on a dielectric barrier discharge for the determination of mercury by atomic emission spectrometry.

    PubMed

    Zhu, Zhenli; Chan, George C-Y; Ray, Steven J; Zhang, Xinrong; Hieftje, Gary M

    2008-11-15

    A low-power, atmospheric-pressure microplasma source based on a dielectric barrier discharge (DBD) has been developed for use in atomic emission spectrometry. The small plasma (0.6 mm x 1 mm x 10 mm) is generated within a glass cell by using electrodes that do not contact the plasma. Powered by an inexpensive ozone generator, the discharge ignites spontaneously, can be easily sustained in Ar or He at gas flow rates ranging from 5 to 200 mL min(-1), and requires less than 1 W of power. The effect of operating parameters such as plasma gas identity, plasma gas flow rate, and residual water vapor on the DBD source performance has been investigated. The plasma can be operated without removal of residual water vapor, permitting it to be directly coupled with cold vapor generation sample introduction. The spectral background of the source is quite clean in the range from 200 to 260 nm with low continuum and structured components. The DBD source has been applied to the determination of Hg by continuous-flow, cold vapor generation and offers detection limits from 14 (He-DBD) to 43 pg mL(-1) (Ar-DBD) without removal of the residual moisture. The use of flow injection with the He-DBD permits measurement of Hg with a 7.2 pg limit of detection, and with repetitive injections having an RSD of <2% for a 10 ng mL(-1) standard.

  9. Adsorption, X-ray Diffraction, Photoelectron, and Atomic Emission Spectroscopy Benchmark Studies for the Eighth Industrial Fluid Properties Simulation Challenge.

    PubMed

    Ross, Richard B; Aeschliman, David B; Ahmad, Riaz; Brennan, John K; Brostrom, Myles L; Frankel, Kevin A; Moore, Jonathan D; Moore, Joshua D; Mountain, Raymond D; Poirier, Derrick M; Thommes, Matthias; Shen, Vincent K; Schultz, Nathan E; Siderius, Daniel W; Smith, Kenneth D

    2016-02-01

    The primary goal of the eighth industrial fluid properties simulation challenge was to test the ability of molecular simulation methods to predict the adsorption of organic adsorbates in activated carbon materials. The challenge focused on the adsorption of perfluorohexane in the activated carbon standard BAM-P109 (Panne and Thünemann 2010). Entrants were challenged to predict the adsorption of perfluorohexane in the activated carbon at a temperature of 273 K and at relative pressures of 0.1, 0.3, and 0.6. The relative pressure (P/Po) is defined as that relative to the bulk saturation pressure predicted by the fluid model at a given temperature (273 K in this case). The predictions were judged by comparison to a set of experimentally determined values, which are published here for the first time and were not disclosed to the entrants prior to the challenge. Benchmark experimental studies, described herein, were also carried out and provided to entrants in order to aid in the development of new force fields and simulation methods to be employed in the challenge. These studies included argon, carbon dioxide, and water adsorption in the BAM-P109 activated carbon as well as X-ray diffraction, X-ray microtomography, photoelectron spectroscopy, and atomic emission spectroscopy studies of BAM-P109. Several concurrent studies were carried out for the BAM-P108 activated carbon (Panne and Thünemann 2010). These are included in the current manuscript for comparison.

  10. Adsorption, X-ray Diffraction, Photoelectron, and Atomic Emission Spectroscopy Benchmark Studies for the Eighth Industrial Fluid Properties Simulation Challenge*+

    PubMed Central

    Ross, Richard B.; Aeschliman, David B.; Ahmad, Riaz; Brennan, John K.; Brostrom, Myles L.; Frankel, Kevin A.; Moore, Jonathan D.; Moore, Joshua D.; Mountain, Raymond D.; Poirier, Derrick M.; Thommes, Matthias; Shen, Vincent K.; Schultz, Nathan E.; Siderius, Daniel W.; Smith, Kenneth D.

    2016-01-01

    The primary goal of the eighth industrial fluid properties simulation challenge was to test the ability of molecular simulation methods to predict the adsorption of organic adsorbates in activated carbon materials. The challenge focused on the adsorption of perfluorohexane in the activated carbon standard BAM-P109 (Panne and Thünemann 2010). Entrants were challenged to predict the adsorption of perfluorohexane in the activated carbon at a temperature of 273 K and at relative pressures of 0.1, 0.3, and 0.6. The relative pressure (P/Po) is defined as that relative to the bulk saturation pressure predicted by the fluid model at a given temperature (273 K in this case). The predictions were judged by comparison to a set of experimentally determined values, which are published here for the first time and were not disclosed to the entrants prior to the challenge. Benchmark experimental studies, described herein, were also carried out and provided to entrants in order to aid in the development of new force fields and simulation methods to be employed in the challenge. These studies included argon, carbon dioxide, and water adsorption in the BAM-P109 activated carbon as well as X-ray diffraction, X-ray microtomography, photoelectron spectroscopy, and atomic emission spectroscopy studies of BAM-P109. Several concurrent studies were carried out for the BAM-P108 activated carbon (Panne and Thünemann 2010). These are included in the current manuscript for comparison. PMID:27840543

  11. Improvement of sensitivity of electrolyte cathode discharge atomic emission spectrometry (ELCAD-AES) for mercury using acetic acid medium.

    PubMed

    Shekhar, R

    2012-05-15

    A method has been developed to improve the sensitivity of the electrolyte cathode discharge atomic emission spectrometry (ELCAD-AES) for mercury determination. Effects of various low molecular weight organic solvents at different volume percentages as well as at different acid molarities on the mercury signal were investigated using ELCAD-AES. The addition of few percent of organic solvent, acetic acid produced significant enhancement in mercury signal. Acetic acid of 5% (v/v) with the 0.2M acidity has been found to give 500% enhancement for mercury signal in flow injection mode. Under the optimized parameters the repeatability, expressed as the percentage relative standard deviation of spectral peak area for mercury with 5% acetic acid was found to be 10% for acid blank solution and 5% for 20 ng/mL mercury standard based on multiple measurements with a multiple sample loading in flow injection mode. Limit of detection of this method was determined to be 2 ng/mL for inorganic mercury. The proposed method has been validated by determining mercury in certified reference materials, Tuna fish (IAEA-350) and Aquatic plant (BCR-060). Accuracy of the method for the mercury determination in the reference materials has been found to be between 3.5% and 5.9%. This study enhances the utility of ELCAD-AES for various types of biological and environmental materials to quantify total mercury at very low levels.

  12. Development of rapid slurry methods for flame and direct current plasma emission and graphite furnace atomic absorption analysis of solid animal tissue

    SciTech Connect

    Fietkau, R.

    1986-01-01

    Studies are presented describing developments in the rapid, direct atomic spectrochemical analysis of meat samples by the technique of slurry atomization. The number of elements that can be determined in meat slurry samples has been increased and the concentration range that can be detected extended to included analysis at the part per billion as well as the percent level. Slurry atomization involves the rapid preparation procedure whereby the sample is simple homogenized with deionized distilled water prior to analysis. In this manner, rapid, quantitative analysis of hot dogs (processed meat) for dietary salt (Na, K) was achieved by premixed air-natural gas flame emission spectrometry. Quantitative analysis of mechanically separated meat for residual bone fragments (as Ca) was attained using a simple photometer when the premixed air-acetylene flame was used. The phosphate interference of the Ca emission signal was overcome by placing an insert in the spray chamber which decreased the droplet size of the aerosol reaching the flame. Slight matrix modification in the form of 2% nitric acid was necessary to solubilize the Ca from the bone fragments. Determining elements present at very low concentrations i.e. part per billion levels, in homogenized beef liver was evaluated using graphite furnace atomic absorption and shown to be viable for determinations of Pb, Cd, Cr, and Ni. Qualitative multielement analysis of several types of meat slurries by direct current plasma (DCP) emission spectrometry using both photographic and electronic modes of detection was reported for the first time.

  13. X-RAY NONLINEAR OPTICAL PROCESSES IN ATOMS USING A SELF-AMPLIFIED SPONTANEOUS EMISSION FREE-ELECTRON LASER

    SciTech Connect

    Rohringer, N

    2008-08-08

    X-ray free electron lasers (xFEL) will open new avenues to the virtually unexplored territory of non-linear interactions of x rays with matter. Initially xFELs will be based on the principle of self-amplified spontaneous emission (SASE). Each SASE pulse consists of a number of coherent intensity spikes of random amplitude, i.e. the process is chaotic and pulses are irreproducible. The coherence time of SASE xFELs will be a few femtoseconds for a photon energy near 1 keV. The importance of coherence properties of light in non-linear optical processes was theoretically discovered in the early 1960s. In this contribution we will illustrate the impact of field chaoticity on x-ray non-linear optical processes on neon for photon energies around 1 keV and intensities up to 10{sup 18} W/cm{sup 2}. Resonant and non-resonant processes are discussed. The first process to be addressed is the formation of a double-core hole in neon by photoionization with x rays above 1.25 keV energy. In contrast to the long-wavelength regime, non-linear optical processes in the x-ray regime are characterized in general by sequential single-photon single-electron interactions. Despite this fact, the sequential absorption of multiple x-ray photons depends on the statistical properties of the radiation field. Treating the x rays generated by a SASE FEL as fully chaotic, a quantum-mechanical analysis of inner-shell two-photon absorption is performed. By solving a system of time-dependent rate equations, we demonstrate that double-core hole formation in neon via x-ray two-photon absorption is enhanced by chaotic photon statistics. At an intensity of 10{sup 16} W/cm{sup 2}, the statistical enhancement is about 30%, much smaller than typical values in the optical regime. The second part of this presentation discusses the resonant Auger effect of atomic neon at the 1s-3p transition (at 867.1 eV). For low X-ray intensity, the excitation process 1s {yields} 3p in Neon can be treated perturbatively. The

  14. Prediction of CO Cameron band and atomic oxygen visible emissions in comets C/2013 A1 (Siding Spring) and 67P/Churyumov-Gerasimenko

    NASA Astrophysics Data System (ADS)

    Raghuram, S.; Bhardwaj, A.

    2014-04-01

    The forbidden emissions of cometary species have special importance in the cometary spectra. The excited species which produce these forbidden emissions can not be populated by direct solar radiation excitation. These metastable species are produced mainly from dissociative excitation and ion-electron recombination reactions. Thus the observed emissions have been used as tracers of parent cometary species. The CO (a3 -X1) is a forbidden transition which produces Cameron band emission in the ultraviolet region during dissociative excitation of CObearing neutrals and the dissociative recombination of CO-ionic species in the cometary coma. Similarly, the forbidden transitions of metastable atomic oxygen 1S-3P (green, 5577 Å), and 1D-3P (red-doublet, 6300 and 6364 Å) produce line emissions in the visible region. These emissions have been used to probe H2O and CO2 abundances in the comets. We have developed a coupled chemistry-emission model to study various production and loss mechanisms of these excited metastable states. The model is applied to comet C/2013 A1 (Siding Spring) which will have a close fly-by of Mars during mid October, 2014, when Indian Mars orbiter Mission and NASA's Maven, would be orbiting the planet. The model is also applied on ESA's Rosetta mission target comet 67P/Churyumov-Gerasimenko which will be useful for different observations over various heliocentric distances. The predicted intensities and quantitative analysis of these emissions can be a theoretical support for various space and ground-based observations.

  15. The Determination of Metals in Sediment Pore Waters and in 1N HCl-Extracted Sediments by ICP-MS

    USGS Publications Warehouse

    May, T.W.; Wiedmeyer, Ray H.; Brumbaugh, W.G.; Schmitt, C.J.

    1997-01-01

    Concentrations of metals in sediment interstitial water (pore water) and those extractable from sediment with weak acids can provide important information about the bioavailability and toxicological effects of such contaminants. The highly variable nature of metal concentrations in these matrices requires instrumentation with the detection limit capability of graphite furnace atomic absorption and the wide dynamic linear range capability of ICP-OES. These criteria are satisfied with ICP-MS instrumentation. We investigated the performance of ICP-MS in the determination of certain metals from these matrices. The results for three metals were compared to those determined by graphite furnace atomic absorption spectroscopy. It was concluded that ICP-MS was an excellent instrumental approach for the determination of metals in these matrices.

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

    PubMed

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

    2011-02-01

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

  17. Comparison of MP AES and ICP-MS for analysis of principal and selected trace elements in nitric acid digests of sunflower (Helianthus annuus).

    PubMed

    Karlsson, Stefan; Sjöberg, Viktor; Ogar, Anna

    2015-04-01

    The use of nitrogen as plasma gas for microwave plasma atomic emission spectroscopy (MP AES) is an interesting development in analytical science since the running cost can be significantly reduced in comparison to the inductively coupled argon plasma. Here, we evaluate the performance of the Agilent 4100 MP AES instrument for the analysis of principal metals (Ca, K, Mg, and Na), lithogenic metals (Al, Fe, and Mn) and selected trace metals (As, Ba, Cd, Co, Cr, Cu, Mo, Ni, Pb, V, and Zn) in nitric acid plant digests. The digests were prepared by microwave-assisted dissolution of dry plant material from sunflower (Helianthus annuus) in concentrated nitric acid. Comparisons are made with analysis of the same solutions with ICP-MS (Agilent 7500cx) using the octopole reaction system (ORS) in the collision mode for As, Fe, and V. The limits of detection were usually in the low µg L(-1) range and all principal and lithogenic metals were successfully determined with the MP AES and provided almost identical results with the ICP-MS. The same applies for the selected trace metals except for As, Co and Mo where the concentrations were below the detection limit with the MP AES. For successful analysis we recommend that (i) only atom lines are used, (ii) ionization is minimized (e.g. addition of CsNO3) and (iii) the use of internal standards should be considered to resolve spectral interferences.

  18. Characterization of polycyclic aromatic hydrocarbon emissions in the particulate and gas phase from smoldering mosquito coils containing various atomic hydrogen/carbon ratios.

    PubMed

    Yang, Tzu-Ting; Lin, Shaw-Tao; Lin, Tser-Sheng; Chung, Hua-Yi

    2015-02-15

    The polycyclic aromatic hydrocarbon emissions in particulate and gas phases generated from smoldering mosquito coils containing various atomic H/C ratios were examined. Five types of mosquito coils were burned in a test chamber with a total airflow rate of 8.0 L/min at a constant relative humidity and temperature. The concentrations of individual PAHs were determined using the GC/MS technique. Among the used mosquito coils, the atomic H/C ratio ranged from 1.23 to 1.57, yielding total mass, gaseous, and particulate PAH emission factors of 28.17-78.72 mg/g, 26,139.80-35,932.98 and 5735.22-13,431.51 ng/g, respectively. The various partitions of PAHs in the gaseous and particulate phases were in the ranges, 70.26-83.70% and 16.30-29.74% for the utilized mosquito coils. The carcinogenic potency of PAH emissions in the particulate phase (203.82-797.76 ng/g) was approximately 6.92-25.08 times higher than that of the gaseous phase (26.27-36.07 ng/g). Based on the analyses of PAH emissions, mosquito coils containing the lowest H/C ratio, a low oxygen level, and additional additives (i.e., CaCO3) are recommended for minimizing the production of total PAH emission factors and carcinogenic potency.

  19. ICPS: an integrative cancer profiler system.

    PubMed

    Zhang, Xin-yu; Shi, Lin; Liu, Yan; Tian, Feng; Zhao, Hai-tao; Miao, Xiao-ping; Huang, Ming-lie; Zhu, Xiao-yan

    2010-10-15

    Founded upon the database of 570 public signatures, ICPS is a web-based application to obtain biomarker profiles among 11 common cancers by integrating genomic alterations with transcription signatures on the basis of a previously developed integrative pipeline. ICPS supports both public data and user's in-house data, and performs meta-analysis at a cancer subtype level by combining heterogeneous datasets. Finally, ICPS returns the robust gene signature containing potential cancer biomarkers that may be useful to carcinogenesis study and clinical cancer diagnosis. http://server.bioicps.org zhxy@mail.tsinghua.edu.cn; zxy-dcs@mail.tsinghua.edu.cn

  20. Multi-element method for determination of trace elements in sunscreens by ICP-AES.

    PubMed

    Zachariadis, G A; Sahanidou, E

    2009-10-15

    An inductively coupled plasma atomic emission spectrometric (ICP-AES) method was developed for multi-element analysis of sunscreen creams and lotions. The objective was the simultaneous determination of Ti (TiO(2) being is the only authorized inorganic UV filter in the European Union) and several minor, trace or toxic elements (Al, Zn, Mg, Fe, Mn, Cu, Cr, Pb and B) in the final products. Two alternative pretreatment procedures were examined: (i) total acid digestion in closed pressurized vessels prior to sample introduction into the plasma and (ii) direct introduction of sample in the form of emulsified slurry. The latter was proved inefficient for several types of creamy samples due to their high viscosity and insolubility. Several acid mixtures were examined for wet digestion because of the complex and fatty matrix of creams and lotions. Plasma parameters like nebulizer argon gas flow rate and radiofrequency incident power were optimized in order to improve the atomization. The recovery of the proposed acid digestion method was evaluated using spiked samples. The calculated recoveries were 95.0% for Ti, 98.2% for Zn and 101.3% for Fe, and the detection limits were 0.2 microg g(-1) for Ti, 0.2 microg g(-1) for Zn and 0.5 microg g(-1) for Fe, respectively. Possible interference from the presence of Ti on the sensitivity of each analyte was examined. Finally the method was applied successfully to several commercial sun protection products and the results were compared with those obtained by atomic absorption spectrometry as reference method.

  1. Shock-tube studies of atomic silicon emission in the spectral range 180 to 300 nm. [environment simulation for Jupiter probes

    NASA Technical Reports Server (NTRS)

    Prakash, S. G.; Park, C.

    1978-01-01

    Emission spectroscopy of shock-heated atomic silicon was performed in the spectral range 180 to 300 nm, in an environment simulating the ablation layer expected around a Jovian entry probe with a silica heat shield. From the spectra obtained at temperatures from 6000 to 10,000 K and electron number densities from 1 quadrillion to 100 quadrillion per cu cm, the Lorentzian line-widths were determined. The results showed that silicon lines are broadened significantly by both electrons (Stark broadening) and hydrogen atoms (Van der Waals broadening), and the combined line-widths are much larger than previously assumed. From the data, the Stark and the Van der Waals line-widths were determined for 34 silicon lines. Radiative transport through a typical shock layer was computed using the new line-width data. The computations showed that silicon emission in the hot region is large, but it is mostly absorbed in the colder region adjacent to the wall.

  2. Development of an international standard for the determination of metals and metalloids in workplace air using ICP-AES: evaluation of sample dissolution procedures through an interlaboratory trial.

    PubMed

    Butler, O T; Howe, A M

    1999-02-01

    Inductively coupled plasma atomic emission spectrometry (ICP-AES) is rapidly overtaking atomic absorption spectrometry (AAS) as the method of choice for the determination of toxic metals in workplace air. However, the few ICP-AES methods that have been published are not well characterised in terms of the effectiveness of the sample dissolution procedures described and their validation status. The International Standards Organization (ISO) is currently engaged in developing ISO 15202, which will describe a generic method for the determination of metals and metalloids in airborne particulate matter by ICP-AES. One part of the proposed standard deals with dissolution procedures. The ISO work has been supported by a project carried out in the authors' laboratory to identify, develop and validate sample dissolution procedures for inclusion in the proposed standard. This paper describes an interlaboratory comparison carried out to assess the performance of selected procedures using samples of airborne particulate matter collected on filters with a multiport sampler. Five dissolution procedures were tested. These included an ultrasonic agitation procedure, two hot-plate procedures (based upon NIOSH 7300 and OSHA ID 125G) and two microwave-assisted procedures (based upon EPA 3052). It was shown that the dissolution procedures selected for use in the trial and used internally at HSL generally gave equivalent performance. As expected, a wider spread of results was obtained by participants in the trial. More specifically, there exists some reservation regarding the ability of the ultrasonic and hot-plate procedures to attack fully on a consistent basis some resistant materials, e.g., chromium containing particulate matter. Above all, the trial demonstrated the usefulness of microwave-assisted dissolution procedures in a modern laboratory.

  3. [The application of inductively coupled plasma atomic emission spectrometry/mass spectrometry to the analysis of advanced ceramic materials].

    PubMed

    Wang, Zheng; Wang, Shi-Wei; Qiu, De-Ren; Yang, Peng-Yuan

    2009-10-01

    Advanced ceramics have been applied to various important fields such as information science, aeronautics and astronautics, and life sciences. However, the optics and electric properties of ceramics are significantly affected by the micro and trace impurities existing in the material even at very low concentration level. Thus, the accurate determination of impurities is important for materials preparation and performance. Methodology of the analysis of advanced ceramic materials using ICP-AES/MS was reviewed in the present paper for the past decade. Various techniques of sample introduction, especially advances in the authors' recent work, are described in detail. The developing trend is also presented. Sixty references are cited.

  4. X-ray emission spectroscopy applied to glycine adsorbed on Cu(110): An atom and symmetry projected view

    SciTech Connect

    Hasselstroem, J.; Karis, O.; Weinelt, M.

    1997-04-01

    When a molecule is adsorbed on a metal surface by chemical bonding new electronic states are formed. For noble and transition metals these adsorption-induced states overlap with the much more intense metal d-valence band, making them difficult to probe by for instance direct photoemission. However, it has recently been shown that X-ray emission spectroscopy (XES) can be applied to adsorbate systems. Since the intermediate state involves a core hole, this technique has the power to project out the partial density of states around each atomic site. Both the excitation and deexcitation processes are in general governed by the dipole selection rules. For oriented system, it is hence possible to obtain a complete separation into 2p{sub x}, 2p{sub y} and 2p{sub z} contributions using angular resolved measurements. The authors have applied XES together with other core level spectroscopies to glycine adsorption on Cu(110). Glycine (NH{sub 2}CH{sub 2}COOH) is the smallest amino acid and very suitable to study by core level spectroscopy since it has several functional groups, all well separated in energy by chemical shifts. Its properties are futhermore of biological interest. In summary, the authors have shown that it is possible to apply XES to more complicated molecular adsorbates. The assignment of different electronic states is however not as straight forward as for simple diatomic molecules. For a complete understanding of the redistribution and formation of new electronic states associated with the surface chemical bond, experimental data must be compared to theoretical calculations.

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

    PubMed

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

    2014-11-01

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

  6. Evaluation of lithium determination in three analyzers: flame emission, flame atomic absorption spectroscopy and ion selective electrode.

    PubMed

    Aliasgharpour, Mehri; Hagani, Hamid

    2009-10-01

    Lithium carbonate salt has become an increasingly important substance in the treatment of manic depressive disorders, and its relatively narrow therapeutic range has caused laboratories to monitor the serum concentration carefully. In the present work we evaluated lithium measurement in 3 different analyzers. METHODS #ENTITYSTARTX00026; Three different analyzers including Flame Emission (FES), Flame Atomic Absorption Spectroscopy (FAAS), and Ion Selective Electrode (ISE) were used. All chemicals had a grade suitable for trace metal analysis. Within-day precision of CV was ≤ 1.5% for FES & FAAS, except for ISE (1.9% CV). Between-days precision of CV was less for FES than for FAAS and ISE (1.3% versus 2.2% & 2.3%). The percent recovery of added lithium in pooled patients' serum was higher for ISE than for FASS and FES (103.4% versus 96.2% and 94.6%). We also obtained a higher average lithium concentration for patients' serum samples (n=16) measured by ISE than for FAAS and FES (0.825±0.30 versus 0.704±0.26 & 0.735±0.19). Paired t-test results revealed a significant difference (p< 0.001) for patient sera analyzed with FAAS and ISE. We report higher results for ISE than the other two analyzers and conclude that the choice between the two flame methods for patients' serum lithium determination is arbitrary and that FES analyzer is a more attractive routine alternative for lithium determination than FAAS because of its cost and ease of performance. In addition, the results obtained by ISE are precise. However, its accuracy may depend on other interfering factors.

  7. The use of ion chromatography-dc plasma atomic emission spectrometry for the speciation of trace metals

    SciTech Connect

    Urasa, I.T.

    1991-09-20

    The original objects of this research program were: to interface d.c. plasma atomic emission spectrometer with an ion chromatograph; to characterize and optimize the combined systems for application in the speciation of metals in aqueous solutions; to use this system in the study of the solution chemistry of various metals; and to find ways in which the measurement sensitivity of the method can be enhanced, thereby allowing the detection of metal species at low ppb concentration levels. This approach has been used to study the chemistry of and speciate several elements in solution including: arsenic, chromium, iron, manganese, nickel phosphorus, platinum, selenium, and vanadium. During the course of this research, we have found that the solution chemistry of the elements studied and the speciation data obtained can vary considerably depending on the solution, and the chromatographic conditions employed. The speciation of chromium, iron, and vanadium was found to be highly influenced by the acidity of the sample. The element selective nature of the d.c. plasma detector allows these changes to be monitored, thereby providing quantitative information on the new moieties formed. New approaches are being developed including the use of chelating ligands as preconcentration agents for purposes of reducing further the detection limits of the elements of interest and to improve the overall element speciation scheme. New thrusts are being directed towards the employment of post-column derivatization method coupled with colorimetric measurements to detect and quantify metal species eluting from the chromatographic column. The influence of sample acidity on these investigations will be carefully evaluated. These new thrusts are described in the accompanying Project Renewal Proposal.

  8. Inductively coupled plasma spectrometry: Noise characteristics of aerosols, application of generalized standard additions method, and Mach disk as an emission source

    SciTech Connect

    Luan, Shen

    1995-10-06

    This dissertation is focused on three problem areas in the performance of inductively coupled plasma (ICP) source. The noise characteristics of aerosols produced by ICP nebulizers are investigated. A laser beam is scattered by aerosol and detected by a photomultiplier tube and the noise amplitude spectrum of the scattered radiation is measured by a spectrum analyzer. Discrete frequency noise in the aerosol generated by a Meinhard nebulizer or a direct injection nebulizer is primarily caused by pulsation in the liquid flow from the pump. A Scott-type spray chamber suppresses white noise, while a conical, straight-pass spray chamber enhances white noise, relative to the noise seen from the primary aerosol. Simultaneous correction for both spectral interferences and matrix effects in ICP atomic emission spectrometry (AES) can be accomplished by using the generalized standard additions method (GSAM). Results obtained with the application of the GSAM to the Perkin-Elmer Optima 3000 ICP atomic emission spectrometer are presented. The echelle-based polychromator with segmented-array charge-coupled device detectors enables the direct, visual examination of the overlapping lines Cd (1) 228.802 nm and As (1) 228.812 nm. The slit translation capability allows a large number of data points to be sampled, therefore, the advantage of noise averaging is gained. An ICP is extracted into a small quartz vacuum chamber through a sampling orifice in a water-cooled copper plate. Optical emission from the Mach disk region is measured with a new type of echelle spectrometer equipped with two segmented-array charge-coupled-device detectors, with an effort to improve the detection limits for simultaneous multielement analysis by ICP-AES.

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

    NASA Astrophysics Data System (ADS)

    Scheffler, Guilherme Luiz; Pozebon, Dirce

    2015-11-01

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

  10. Methods of atomic oxygen and ozone retrieval from observations of the O2 dayglow emissions in the MLT region

    NASA Astrophysics Data System (ADS)

    Yankovsky, Valentine; Martyshenko, Kseniia; Manuilova, Rada

    2015-04-01

    The problem of creating the new methods of remote sensing of altitude profile of the [O(3P)] and [O3] in the daytime is actual for the mesosphere and lower thermosphere range. Currently there is no reliable method for remote sensing of altitude profile of the [O(3P)], but atomic oxygen is a key component in the mechanism of the atmosphere cooling by quenching of vibrationally excited CO2 molecules and also one of basic quencher of excited components in MLT region. The airglow emission in 1.27 µm IR Atm(0 - 0) band from [O2(a1Δg, v=0)] has been used as a proxy for [O3] in MLT for over a decade. However, lifetime of O2(a1Δg, v=0) is more than 1 hour, therefore this method is not suitable for detecting of relatively rapid [O3] variations which occur due to the variability of the solar spectrum in the UV range (120 - 320 nm) and other space factors. The aim of this study is revealing of proxies for retrievals of [O(3P)] and [O3]. In the framework of developed model of electronic vibrational kinetics of excited products of O3 and O2 photolysis in MLT of the Earth (model YM-2011) [1] we consider the photolysis of O2 in the Schumann-Runge continuum and Lyaman-A H atom and of O3 in Hartley band and for excited products of photolysis ( O2(a1Δg, v=0 - 5), O2(b1Σ+g, v=0, 1, 2) and excited oxygen atom O(1D)) we took into account more than 60 aeronomical reactions of photoexcitation and deexcitation by energy transfer between the excited levels and of quenching of the levels in collisions with O(3P) O2, N2, O(3P), O3, CO2. We tested 5 excited components, namely, O2(b1Σ+g, v=0, 1, 2), O2(a1Δg, v=0 - 5) and O(1D) as the O(3P) and O3 proxies. The total system of kinetic equations for 10 components has been solved and altitude profiles of concentrations of O(1D), O2(b1Σ+g, v=0, 1, 2), and O2(a1Δg, v=0 - 5) have been calculated. To compare characteristics of assumed proxies we used sensitivity analysis of the proxy concentrations altitude profiles to variations of [O3] and

  11. Identification of a single light atom within a multinuclear metal cluster using valence-to-core X-ray emission spectroscopy.

    PubMed

    Delgado-Jaime, Mario Ulises; Dible, Benjamin R; Chiang, Karen P; Brennessel, William W; Bergmann, Uwe; Holland, Patrick L; DeBeer, Serena

    2011-11-07

    Iron valence-to-core Fe Kβ X-ray emission spectroscopy (V2C XES) is established as a means to identify light atoms (C, N, O) within complex multimetallic frameworks. The ability to distinguish light atoms, particularly in the presence of heavier atoms, is a well-known limitation of both crystallography and EXAFS. Using the sensitivity of V2C XES to the ionization potential of the bound ligand, energetic shifts of ~10 eV in the ligand 2s ionization energies of bound C, N, and O may be observed. As V2C XES is a high-energy X-ray method, it is readily applicable to samples in any physical form. This method thus has great potential for application to multimetallic inorganic frameworks involved in both small molecule storage and activation. © 2011 American Chemical Society

  12. ICP Reactor Modeling: CF4 Discharge

    NASA Technical Reports Server (NTRS)

    Bose, Deepak; Govindan, T. R.; Meyyappan, M.

    1999-01-01

    Inductively coupled plasma (ICP) reactors are widely used now for etching and deposition applications due to their simpler design compared to other high density sources. Plasma reactor modeling has been playing an important role since it can, in principle, reduce the number of trial and error iterations in the design process and provide valuable understanding of mechanisms. Fluorocarbon precursors have been the choice for oxide etching. We have data available on CF4 from our laboratory. These are current voltage characteristics, La.ngmuir probe data, UV-absorption, and mass spectrometry measurements in a GEC-ICP reactor. We have developed a comprehensive model for ICP reactors which couples plasma generation and transport and neutral species dynamics with the gas flow equations. The model has been verified by comparison with experimental results for a nitrogen discharge in an ICP reactor. In the present work, the model has been applied to CF4 discharge and compared to available experimental data.

  13. Selected problems with boron determination in water treatment processes. Part I: comparison of the reference methods for ICP-MS and ICP-OES determinations.

    PubMed

    Kmiecik, Ewa; Tomaszewska, Barbara; Wątor, Katarzyna; Bodzek, Michał

    2016-06-01

    The aim of the study was to compare the two reference methods for the determination of boron in water samples and further assess the impact of the method of preparation of samples for analysis on the results obtained. Samples were collected during different desalination processes, ultrafiltration and the double reverse osmosis system, connected in series. From each point, samples were prepared in four different ways: the first was filtered (through a membrane filter of 0.45 μm) and acidified (using 1 mL ultrapure nitric acid for each 100 mL of samples) (FA), the second was unfiltered and not acidified (UFNA), the third was filtered but not acidified (FNA), and finally, the fourth was unfiltered but acidified (UFA). All samples were analysed using two analytical methods: inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma optical emission spectrometry (ICP-OES). The results obtained were compared and correlated, and the differences between them were studied. The results show that there are statistically significant differences between the concentrations obtained using the ICP-MS and ICP-OES techniques regardless of the methods of sampling preparation (sample filtration and preservation). Finally, both the ICP-MS and ICP-OES methods can be used for determination of the boron concentration in water. The differences in the boron concentrations obtained using these two methods can be caused by several high-level concentrations in selected whole-water digestates and some matrix effects. Higher concentrations of iron (from 1 to 20 mg/L) than chromium (0.02-1 mg/L) in the samples analysed can influence boron determination. When iron concentrations are high, we can observe the emission spectrum as a double joined and overlapping peak.

  14. Using ICP and micro-PIXE to investigate possible differences in the mineral composition of genetically modified versus wild-type sorghum grain

    NASA Astrophysics Data System (ADS)

    Ndimba, R.; Cloete, K.; Mehlo, L.; Kossmann, J.; Mtshali, C.; Pineda-Vargas, C.

    2017-08-01

    In the present study, possible differences in the mineral composition of transgenic versus non-transgenic sorghum grains were investigated using inductively coupled atomic emission spectroscopy (ICP-AES); and, in-tissue elemental mapping by micro Proton-Induced X-ray Emission (micro-PIXE) analysis. ICP AES was used to analyse the bulk mineral content of the wholegrain flour derived from each genotype; whilst micro-PIXE was used to interrogate localised differences in mineral composition specific to certain areas of the grain, such as the bran layer and the central endosperm tissue. According to the results obtained, no significant difference in the average Fe, Zn or Ca content was found to differentiate the transgenic from the wild-type grain using ICP-AES. However, using micro-PIXE, a significant reduction in zinc could be detected in the bran layer of the transgenic grains relative to wild-type. Although it is difficult to draw firm conclusions, as a result of the small sample size used in this study, micro-PIXE has nonetheless proven itself as a useful technique for highlighting the possibility that there may be reduced levels of zinc accumulation in the bran layer of the transgenic grains. Given that the genetic modification targets proteins that are highly concentrated in certain parts of the bran tissue, it seems plausible that the reduced levels of zinc may be an unintended consequence of the silencing of kafirin proteins. Although no immediate health or nutritional concerns emerge from this preliminary finding, it is noted that zinc plays an important biological role within this part of the grain as a structural stabiliser and antioxidant factor. Further study is therefore needed to assess more definitively the extent of the apparent localised reduction in zinc in the transgenic grains and how this may affect other important grain quality characteristics.

  15. Infrared (1-12 μm) atomic and molecular emission signatures from energetic materials using laser-induced breakdown spectroscopy

    NASA Astrophysics Data System (ADS)

    Kumi Barimah, E.; Hömmerich, U.; Brown, E.; Yang, C. S.-C.; Trivedi, S. B.; Jin, F.; Wijewarnasuriya, P. S.; Samuels, A. C.; Snyder, A. P.

    2013-05-01

    Laser-induced breakdown spectroscopy (LIBS) is a powerful analytical technique to detect the elemental composition of solids, liquids, and gases in real time. For example, recent advances in UV-VIS LIBS have shown great promise for applications in chemical, biological, and explosive sensing. The extension of conventional UVVIS LIBS to the near-IR (NIR), mid-IR (MIR) and long wave infrared (LWIR) regions (~1-12 μm) offers the potential to provide additional information due to IR atomic and molecular signatures. In this work, a Q-switched Nd: YAG laser operating at 1064 nm was employed as the excitation source and focused onto several chlorate and nitrate compounds including KClO3, NaClO3, KNO3, and NaNO3 to produce intense plasma at the target surface. IR LIBS studies on background air, KCl , and NaCl were also included for comparison. All potassium and sodium containing samples revealed narrow-band, atomic-like emissions assigned to transitions of neutral alkali-metal atoms in accordance with the NIST atomic spectra database. In addition, first evidence of broad-band molecular LIBS signatures from chlorate and nitrate compounds were observed at ~10 μm and ~7.3 μm, respectively. The observed molecular emissions showed strong correlation with FTIR absorption spectra of the investigated materials.

  16. Enhancement of Raman scattering for an atom or molecule near a metal nanocylinder: Quantum theory of spontaneous emission and coupling to surface plasmon modes

    NASA Astrophysics Data System (ADS)

    Zuev, V. S.; Frantsesson, A. V.; Gao, J.; Eden, J. G.

    2005-06-01

    An analytic expression for the electromagnetic enhancement of the spontaneous emission rate and Raman scattering cross-section for an excited atom or molecule in close proximity to a metal nanocylinder has been derived by quantum theory. Coupling of the atomic or molecular optical radiation into the TM0 surface plasmon mode of the nanocylinder results in reradiation by the cylinder, a process that is most efficient when the incident radiation is linearly polarized, with the electric field oriented parallel to the axis of the nanocylinder. For a silver cylinder having a radius and length of 5 and 20nm, respectively, the enhancement in the spontaneous emission rate is >107 for ℏω0≃2.4eV (λ =514nm), which corresponds to an increase of ≈1014 in the Raman scattering cross section. This result, as well as the prediction that the atomic dipole generates broadband, femtosecond pulses, are in qualitative agreement with previously reported experiments involving metal nanoparticle aggregates. The theoretical results described here are expected to be of value in guiding future nonlinear optical experiments in which carbon nanotubes or metal nanowires with controllable physical and electrical characteristics are patterned onto a substrate and coupled with emitting atoms or molecules.

  17. ICP polishing of silicon for high-quality optical resonators on a chip

    NASA Astrophysics Data System (ADS)

    Laliotis, A.; Trupke, M.; Cotter, J. P.; Lewis, G.; Kraft, M.; Hinds, E. A.

    2012-12-01

    Miniature concave hollows, made by wet etching silicon through a circular mask, can be used as mirror substrates for building optical micro-cavities on a chip. In this paper, we investigate how inductively coupled plasma (ICP) polishing improves both shape and roughness of the mirror substrates. We characterize the evolution of the surfaces during the ICP polishing using white-light optical profilometry and atomic force microscopy. A surface roughness of 1 nm is reached, which reduces to 0.5 nm after coating with a high reflectivity dielectric. With such smooth mirrors, the optical cavity finesse is now limited by the shape of the underlying mirror.

  18. A comparison of simultaneous plasma, atomic absorption, and iron colorimetric determinations of major and trace constituents in acid mine waters

    USGS Publications Warehouse

    Ball, J.W.; Nordstrom, D.K.

    1994-01-01

    Sixty-three water samples collected during June to October 1982 from the Leviathan/Bryant Creek drainage basin were originally analyzed by simultaneous multielement direct-current plasma (DCP) atomic-emission spectrometry, flame atomic-absorption spectrometry, graphite-furnace atomic-absorption spectrometry (GFAAS) (thallium only), ultraviolet-visible spectrometry, and hydride-generation atomic-absorption spectrometry.Determinations were made for the following metallic and semi-metallic constituents: AI, As, B, Ba, Be, Bi, Cd, Ca, Cr, Co, Cu, Fe(11), Fe(total), Li, Pb, Mg, Mn, Mo, Ni, K, Sb, Se, Si, Na, Sr, TI, V, and Zn. These samples were re-analyzed later by simultaneous multielement inductively coupled plasma (ICP) atomic-emission spectrometry and Zeeman-corrected GFAAS to determine the concentrations of many of the same constituents with improved accuracy, precision, and sensitivity. The result of this analysis has been the generation of comparative concentration values for a significant subset of the solute constituents. Many of the more recently determined values replace less-than-detection values for the trace metals; others constitute duplicate analyses for the major constituents. The multiple determinations have yielded a more complete, accurate, and precise set of analytical data. They also have resulted in an opportunity to compare the performance of the plasma-emission instruments operated in their respective simultaneous multielement modes. Flame atomic-absorption spectrometry was judged best for Na and K and hydride-generation atomic-absorption spectrometry was judged best for As because of their lower detection limit and relative freedom from interelement spectral effects. Colorimetric determination using ferrozine as the color agent was judged most accurate, precise, and sensitive for Fe. Cadmium, lead, and vanadium concentrations were too low in this set of samples to enable a determination of whether ICP or DCP is a more suitable technique. Of

  19. [Analysis of macroelements and microelements in Chinese traditional medicine Plumbago zeylanica Linn by ICP-AES].

    PubMed

    Tan, Ming-xiong; Chen, Zhen-feng; Wang, Heng-shan; Liu, Yan-cheng; Liang, Hong

    2009-04-01

    Twenty macroelements and microelements were analyzed in the leaves, stems and roots of Plumbago zeylanica Linn from Guangxi by inductively.coupled plasma atomic emission spectrometry (ICP-AES). Four macroelements, Na, K, Ca and Mg, five essential microelements, Zn, Fe, Mn, Cr and Co, and eight other elements, Mo, Sb, Bi, Cd, Sr, Pb, Cd and As, were detected in all samples. The contents of the elements are varied in different parts of P. zeylanica. For all the determined elements, the contents in the leaves and roots are relatively higher as compared to those in the stems and it is in concurrence with the active parts of Plumbago zeylanica for the cure of antioxidant and anticancer drugs, as the elements Na, K, Ca, Zn, Fe, Mn, Sr, Cu and Co are the highest in leaves, followed by those is in roots. Many anticancer herbs usually show comparatively rich Zn, Mn, Fe, as well as Cr,Sr and Cu. Plumbago zeylanica exists with abundant Zn, Mn and Fe and a certain amount of Cr, Sr and Cu. The results would provide useful data for discussing the relationship between the elements in Chinese traditional medicine and its activities, and could be useful for the exploitation of the Chinese traditional medicinal resources.

  20. Boron-10 analyses using prompt gamma neutron activation and ICP-AES

    SciTech Connect

    Riley, K.J.; Harling, O.K.

    1996-12-31

    Boron-10 quantification is a vital part of the phase I clinical trials that are in progress under the Massachusetts Institute of Technology (MIT)/New England Deaconess Hospital (NEDH) joint BNCT project. Accurate knowledge of the {sup 10}B content of blood as a function of time and immediately prior to irradiation is needed to calculate the total dose delivered to healthy tissue. The MIT/NEDH group continually seeks to improve and refine quantification methods to achieve greater sensitivity and faster analysis time. Rapid analysis is desirable so that irradiation can be initiated quickly, while high sensitivity will be needed to analyze very small samples. Brain tumor biopsies may be quite small, especially in cases where the tumor is not resectable. An upgraded version of the MIT prompt gamma neutron activation analysis (PGNAA) facility and an inductively coupled plasma atomic emission spectroscopy (ICP-AES) machine with a high-efficiency nebulizer (HEN) have been used to analygze {sup 10}B content in small samples down to the size range of needle biopsies ({approx} 0.03 ml).

  1. Trace element determination of Argentine wines using ETAAS and USN-ICP-OES.

    PubMed

    Lara, R; Cerutti, S; Salonia, J A; Olsina, R A; Martinez, L D

    2005-02-01

    The objective of this work was to develop a method to determine the metal content in wine samples from the province of Mendoza in Argentina. Ten samples of white wine and 10 samples of red wine available in the supermarket were analyzed for the metals aluminium, cadmium, calcium, chromium, copper, iron, nickel, lead and zinc by electrothermal atomic spectrometry (ETAAS) and ultrasonic nebulization was coupled to inductively coupled plasma optical emission spectrometry (USN-ICP-OES). The aluminium, cadmium, calcium, copper, iron, lead, zinc, chromium concentrations were between 17.0-18.0 microg l(-1), 1.0-4.7microg l(-1), 10.0-15.0 mg l(-1), 23.0-28.0 microg l(-1), 480-790 microg l(-1), 50-90 microg l(-1), 24-130 microg l(-1), and <0.2-6.25 microg l(-1), respectively. The levels compare well with those reported for similar wines from some other parts of the world. A significant aspect in this paper is the samples mineralization step, which allowed the direct determination of the metals. Concerning to the Cd determination, a refluxing digestion system was used for the pretreatment of the samples.

  2. Simplified multi-element analysis of ground and instant coffees by ICP-OES and FAAS.

    PubMed

    Szymczycha-Madeja, Anna; Welna, Maja; Pohl, Pawel

    2015-01-01

    A simplified alternative to the wet digestion sample preparation procedure for roasted ground and instant coffees has been developed and validated for the determination of different elements by inductively coupled plasma optical emission spectrometry (ICP-OES) (Al, Ba, Cd, Co, Cr, Cu, Mn, Ni, Pb, Sr, Zn) and flame atomic absorption spectrometry (FAAS) (Ca, Fe, K, Mg, Na). The proposed procedure, i.e. the ultrasound-assisted solubilisation in aqua regia, is quite fast and simple, requires minimal use of reagents, and demonstrated good analytical performance, i.e. accuracy from -4.7% to 1.9%, precision within 0.5-8.6% and recovery in the range 93.5-103%. Detection limits of elements were from 0.086 ng ml(-1) (Sr) to 40 ng ml(-1) (Fe). A preliminary classification of 18 samples of ground and instant coffees was successfully made based on concentrations of selected elements and using principal component analysis and hierarchic cluster analysis.

  3. Abundant Acceptor Emission from Nitrogen-Doped ZnO Films Prepared by Atomic Layer Deposition under Oxygen-Rich Conditions.

    PubMed

    Guziewicz, E; Przezdziecka, E; Snigurenko, D; Jarosz, D; Witkowski, B S; Dluzewski, P; Paszkowicz, W

    2017-08-09

    Nitrogen-doped and undoped ZnO films were grown by thermal atomic layer deposition (ALD) under oxygen-rich conditions. Low-temperature photoluminescence spectra reveal a dominant donor-related emission at 3.36 eV and characteristic acceptor-related emissions at 3.302 and 3.318 eV. Annealing at 800 °C in oxygen atmosphere leads to conversion of conductivity from n- to p-type, which is reflected in photoluminescence spectra. Annealing does not increase any acceptor-related emission in the undoped sample, while in the ZnO:N it leads to a considerable enhancement of the photoluminescence at 3.302 eV. The high resolution cathodoluminescence cross-section images show different spatial distribution of the donor-related and the acceptor-related emissions, which complementarily contribute to the overall luminescence of the annealed ZnO:N material. Similar area of both emissions indicates that the acceptor luminescence comes neither from the grain boundaries nor from stacking faults. Moreover, in ZnO:N the acceptor-emission regions are located along the columns of growth, which shows a perspective to achieve a ZnO:N material with homogeneous acceptor conductivity at least at the micrometer scale.

  4. QED Theory of Radiation Emission and Absorption Lines for Atoms and Ions in a Strong Laser Field

    SciTech Connect

    Glushkov, A. V.

    2008-10-22

    The results of numerical calculating the multi-photon resonance shift and width for transition 6S-6F in the atom of Cs (wavelength 1059nm) in a laser pulse of the Gaussian and soliton-like shapes are presented. QED theory of radiation atomic lines is used.

  5. Mobile fiber optic emission spectrograph

    SciTech Connect

    Spencer, W.A.; Coleman, C.J.; McCarty, J.E.; Beck, R.S.

    1997-05-01

    Technical Assistance Request HLW/DWPF-TAR-970064 asked SRTC to evaluate the use of a fiber optic coupled emission spectrometer. The spectrometer would provide additional ICP analyses in the DWPF laboratory.

  6. Ignition Delay in a Pulsed Inductively Coupled Plasma (ICP) in Tandem with an Auxiliary ICP

    NASA Astrophysics Data System (ADS)

    Donnelly, Vincent M.; Liu, Lei; Sridhar, Shyam; Economou, Demetre J.

    2015-09-01

    Plasma ignition delays were observed in a ``main'' ICP, in tandem with an ``auxiliary'' ICP. The Faraday-shielded ICPs were separated by a grounded metal grid. Power (13.56 MHz) to the main ICP was pulsed with a frequency of 1 kHz, while the auxiliary ICP was operated in continuous wave (cw) mode. In chlorine plasmas, ignition delay was observed for duty cycles greater than 60% and, in contrast to expectation, the delay was longer with increasing duty cycle up to ~ 99.5%. The ignition delay could be manipulated by changing the auxiliary and/or main ICP power. Langmuir probe measurements provided the temporal evolution of electron temperature, and electron and positive ion (n+) densities. These measurements revealed that the plasma was re-ignited shortly after the decaying n+ in the main ICP reached the density (n+,aux) measured when only the auxiliary ICP was powered. At that time, the depressed electron density increased sharply resulting in plasma re-ignition. Plasma ignition delay occurred when the afterglow of the pulsed plasma was not long enough for n+ to reach n+,aux during the afterglow. Besides Cl2, plasma ignition delays were also observed in other electronegative gases (SF6, CF4/O2 and O2) but not in an electropositive gas (Ar).

  7. Radionuclide detection by inductively coupled plasma mass spectrometry: A comparison of atomic and radiation detection method

    SciTech Connect

    Smith, M.R.; Wyse, E.J.; Koppenaal, D.W.

    1991-04-01

    Radionuclide detection by mass spectrometric techniques offers inherent advantages over conventional radiation detection methods. Since radionuclides decay at variable rates (half-lives) and via various nuclear transformations (i.e. emission of alpha, beta, and/or gamma radiation) their determination via radiation detection depends not only on decay systematics but also on detector technology. Radionuclide detection by direct atom measurement, however, is dependent only on technique sensitivity and is indifferent to decay mode. Evaluation of inductively coupled plasma mass spectrometry (ICP/MS) indicates this method to be superior conventional radiation detection techniques for many radionuclides. This work discusses factors which influence detection by both methods. Illustrative applications of ICP/MS to the ultra-trace determination of several radionuclides, including {sup 129}I, are presented. 20 refs., 6 figs., 1 tab.

  8. Ignition delay of a pulsed inductively coupled plasma (ICP) in tandem with an auxiliary ICP

    NASA Astrophysics Data System (ADS)

    Liu, Lei; Sridhar, Shyam; Donnelly, Vincent M.; Economou, Demetre J.

    2015-12-01

    Plasma ignition delays were observed in a ‘main’ inductively coupled plasma (ICP), in tandem with an ‘auxiliary’ ICP. The Faraday-shielded ICPs were separated by a grounded metal grid. Power (13.56 MHz) to the main ICP was pulsed with a frequency of 1 kHz, while the auxiliary ICP was operated in continuous wave (cw) mode. In chlorine plasmas, ignition delay was observed for duty cycles greater than 60% and, in contrast to expectation, the delay was longer with increasing duty cycle up to ~99.5%. The ignition delay could be varied by changing the auxiliary and/or main ICP power. Langmuir probe measurements provided the temporal evolution of electron temperature, and electron and positive ion densities. These measurements revealed that the plasma was ignited shortly after the decaying positive ion density (n +), in the afterglow of the main ICP, reached the density ({{n}+},\\text{aux} ) prevailing when only the auxiliary ICP was powered. At that time, production of electrons began to dominate their loss in the main ICP, due to hot electron injection from the auxiliary ICP. As a result, {{n}\\text{e}} increased from a value below {{n}\\text{e,\\text{aux}}} , improving inductive power coupling efficiency, further increasing plasma density leading to plasma ignition. Plasma ignition delay occurred when the afterglow of the pulsed plasma was not long enough for the ion density to reach {{n}+},\\text{aux} during the afterglow. Besides Cl2, plasma ignition delays were also observed in other electronegative gases (SF6, CF4/O2 and O2) but not in an electropositive gas (Ar).

  9. HERSCHEL KEY PROGRAM, ''DUST, ICE, AND GAS IN TIME'' (DIGIT): THE ORIGIN OF MOLECULAR AND ATOMIC EMISSION IN LOW-MASS PROTOSTARS IN TAURUS

    SciTech Connect

    Lee, Jeong-Eun; Lee, Seokho; Lee, Jinhee; Evans II, Neal J.; Green, Joel D.

    2014-10-01

    Six low-mass embedded sources (L1489, L1551-IRS5, TMR1, TMC1-A, L1527, and TMC1) in Taurus have been observed with Herschel-PACS to cover the full spectrum from 50 to 210 μm as part of the Herschel key program, ''Dust, Ice, and Gas In Time''. The relatively low intensity of the interstellar radiation field surrounding Taurus minimizes contamination of the [C II] emission associated with the sources by diffuse emission from the cloud surface, allowing study of the [C II] emission from the source. In several sources, the [C II] emission is distributed along the outflow, as is the [O I] emission. The atomic line luminosities correlate well with each other, as do the molecular lines, but the atomic and molecular lines correlate poorly. The relative contribution of CO to the total gas cooling is constant at ∼30%, while the cooling fraction by H{sub 2}O varies from source to source, suggesting different shock properties resulting in different photodissociation levels of H{sub 2}O. The gas with a power-law temperature distribution with a moderately high density can reproduce the observed CO fluxes, indicative of CO close to LTE. However, H{sub 2}O is mostly subthermally excited. L1551-IRS5 is the most luminous source (Ł{sub bol} = 24.5 L {sub ☉}) and the [O I] 63.1 μm line accounts for more than 70% of its FIR line luminosity, suggesting complete photodissociation of H{sub 2}O by a J shock. In L1551-IRS5, the central velocity shifts of the [O I] line, which exceed the wavelength calibration uncertainty (∼70 km s{sup –1}) of PACS, are consistent with the known redshifted and blueshifted outflow direction.

  10. [Determination of trace lead in traditional Chinese herbal medicine Astragalus by microwave digestion-CTAB enhancing-continual flow ingection hydride generation-ICP-AES].

    PubMed

    Liu, Dong-Lian; Ke, Shao-Ying; Ye, Rong; Ding, Ming-Yu

    2007-11-01

    A new method using microwave digestion technique was developed for the determination of lead in Astragalus by CTAB enhancing-continual flow hydride generation-inductively coupled plasma atomic emission spectrometry (HG-ICP-AES). The experimental conditions of microwave digestion and hydride generation were optimized. This method shows a linear range of 0.23-800 microg x L(-1) and the correlation coefficient is 0.999 9. It is satisfactory to apply the microwave digestion procedure to the determination of Pb under the optimized conditions. The detection limit of the method is 0.23 microg x L(-1) and the RSD is 1.02%. The recovery obtained is 98.8%-100.1%. The results show that this method is rapid and simple with low environmental contamination and complete digestion of samples.

  11. Low Altitude Emission (LAE) of Energetic Neutral Atoms (ENA) Observed by TWINS and its Relation to the CINEMA CubeSat Mission

    NASA Astrophysics Data System (ADS)

    Bazell, D.; Sotirelis, T.; Nair, H.; Roelof, E. C.; Brandt, P. C.

    2009-12-01

    The brightest source of energetic neutral atoms (ENAs) at energies >1keV is low altitude emission (LAE) from ~200-400km near auroral latitudes where precipitating energetic ions undergo multiple atomic collisions with the monatomic (O) exosphere. This emission is many times brighter than that from the high-altitude ring current region where the energetic ions interact only weakly with the much less dense monatomic (H) hydrogen geocorona. The recently selected NSF CubeSat mission CINEMA [Lin et al., this special session] has, as part of its science payload (STEIN), an ENA imager covering energies 4-100keV. From a high-inclination ~800km orbit, STEIN will view the LAE four times during every 90 minutes. The NASA TWINS stereo ENA imagers (2-40keV) will also view the LAE from their Molniya orbits (apogee radius~7Re). We have been analyzing the TWINS ENA images of LAE and comparing them with in situ ion measurements (1-40keV) from DMSP spacecraft when their tracks take them under the ion precipitation regions imaged by TWINS. We have developed an ENA emissivity function that relates the directionally-dependent emergent ENA spectrum to that of the precipitating ions. The TWINS/DMSP direct comparisons show good agreement. We offer suggestions on joint observing strategies for CINEMA, TWINS and DMSP after the CINEMA launch in the second half of 2011.

  12. Non-local-thermodynamical-equilibrium effects in the x-ray emission of radiatively heated materials of different atomic numbers

    NASA Astrophysics Data System (ADS)

    Földes, I. B.; Eidmann, K.; Veres, G.; Bakos, J. S.; Witte, K.

    2001-07-01

    X-ray self-emission of radiatively heated materials with different values of Z has been investigated. Thin foils were uniformly heated by a 120-eV Hohlraum radiation of 400-ps duration in order to study the self-emission of a homogeneous, optically thin material. The x-ray emission spectra were followed for more than 2 ns. The spectrally integrated emission shows not only a strong Z dependence, but different temporal behaviors for different values of Z. The lower is the value of Z of the x-ray heated matter, the longer is the duration of self-emission. Theoretical comparison with a hydrocode and FLY post-processing shows a non-local-thermal equilibrium behavior caused by direct photoionization due to the thermal pumping radiation, which has a higher brightness temperature than the matter temperature of the heated material.

  13. Short-range surface plasmonics: Localized electron emission dynamics from a 60-nm spot on an atomically flat single-crystalline gold surface.

    PubMed

    Frank, Bettina; Kahl, Philip; Podbiel, Daniel; Spektor, Grisha; Orenstein, Meir; Fu, Liwei; Weiss, Thomas; Horn-von Hoegen, Michael; Davis, Timothy J; Meyer Zu Heringdorf, Frank-J; Giessen, Harald

    2017-07-01

    We experimentally and theoretically visualize the propagation of short-range surface plasmon polaritons using atomically flat single-crystalline gold platelets on silicon substrates. We study their excitation and subfemtosecond dynamics via normal-incidence two-photon photoemission electron microscopy. By milling a plasmonic disk and grating structure into a single-crystalline gold platelet, we observe nanofocusing of the short-range surface plasmon polariton. Localized two-photon ultrafast electron emission from a spot with a smallest dimension of 60 nm is observed. Our novel approach opens the door toward reproducible plasmonic nanofocusing devices, which do not degrade upon high light intensity or heating due to the atomically flat surface without any tips, protrusions, or holes. Our nanofoci could also be used as local emitters for ultrafast electron bunches in time-resolved electron microscopes.

  14. Quantitative Determination of Density of Ground State Atomic Oxygen from Both TALIF and Emission Spectroscopy in Hot Air Plasma Generated by Microwave Resonant Cavity

    NASA Astrophysics Data System (ADS)

    Marchal, F.; Yousfi, M.; Merbahi, N.; Wattieaux, G.; Piquemal, A.

    2016-03-01

    Two experimental techniques have been used to quantify the atomic oxygen density in the case of hot air plasma generated by a microwave (MW) resonant cavity. The latter operates at a frequency of 2.45 GHz inside a cell of gas conditioning at a pressure of 600 mbar, an injected air flow of 12 L/min and an input MW power of 1 kW. The first technique is based on the standard two photon absorption laser induced fluorescence (TALIF) using xenon for calibration but applied for the first time in the present post discharge hot air plasma column having a temperature of about 4500 K near the axis of the nozzle. The second diagnostic technique is an actinometry method based on optical emission spectroscopy (OES). In this case, we compared the spectra intensities of a specific atomic oxygen line (844 nm) and the closest wavelength xenon line (823 nm). The two lines need to be collected under absolutely the same spectroscopic parameters. The xenon emission is due to the addition of a small proportion of xenon (1% Xe) of this chemically inert gas inside the air while a further small quantity of H2 (2%) is also added in the mixture in order to collect OH(A-X) and NH(A-X) spectra without noise. The latter molecular spectra are required to estimate gas and excitation temperatures. Optical emission spectroscopy measurements, at for instance the position z=12 mm on the axis plasma column that leads to a gas measured temperature equal to 3500 K, an excitation temperature of about 9500 K and an atomic oxygen density 2.09×1017±0.2×1017 cm-3. This is in very good agreement with the TALIF measurement, which is equal to 2.0×1017 cm-3.

  15. The study on air pollution with nickel and vanadium in Croatia by using moss biomonitoring and ICP-AES.

    PubMed

    Vučković, Ivana; Špirić, Zdravko; Stafilov, Trajče; Kušan, Vladimir; Bačeva, Katerina

    2013-10-01

    Moss samples were collected from 121 sampling sites all over Croatia during the summer and autumn of 2010. They were totally digested by using microwave digestion system and analysed by using atomic emission spectrometry with inductively coupled plasma (ICP-AES). Descriptive statistics and maps of distribution were made. The data obtained in this study were compared with those from the study in 2006 and additionally with the data obtained in the similar studies in neighbouring countries and Norway as pristine area. The median value of nickel is 3.16 mg kg(-1) and the content varies from 1.04 to 14.66 mg kg(-1). The content of vanadium ranges between 0.23 and 37.26 mg kg(-1) with the median value of 2.55 mg kg(-1). High contents of these elements are found in the vicinity of Rijeka, Zagreb and Sisak as a result of their emission from oil refinery, thermal power plant and industrial processes.

  16. Go-ICP: A Globally Optimal Solution to 3D ICP Point-Set Registration.

    PubMed

    Yang, Jiaolong; Li, Hongdong; Campbell, Dylan; Jia, Yunde

    2016-11-01

    The Iterative Closest Point (ICP) algorithm is one of the most widely used methods for point-set registration. However, being based on local iterative optimization, ICP is known to be susceptible to local minima. Its performance critically relies on the quality of the initialization and only local optimality is guaranteed. This paper presents the first globally optimal algorithm, named Go-ICP, for Euclidean (rigid) registration of two 3D point-sets under the L2 error metric defined in ICP. The Go-ICP method is based on a branch-and-bound scheme that searches the entire 3D motion space SE(3). By exploiting the special structure of SE(3) geometry, we derive novel upper and lower bounds for the registration error function. Local ICP is integrated into the BnB scheme, which speeds up the new method while guaranteeing global optimality. We also discuss extensions, addressing the issue of outlier robustness. The evaluation demonstrates that the proposed method is able to produce reliable registration results regardless of the initialization. Go-ICP can be applied in scenarios where an optimal solution is desirable or where a good initialization is not always available.

  17. Determination of trace amounts of molybdenum in plant tissue by solvent extraction-atomic-absorption and direct-current plasma emission spectrometry.

    PubMed

    Lajunen, L H; Kubin, A

    1986-03-01

    Methods are presented for determination of molybdenum in plant tissue by flame and graphite-furnace atomic-absorption spectrometry and direct-current argon-plasma emission spectrometry. The samples are digested in HNO(3)-H(2)SO(4)-HC1O(4) mixture, and Mo is separated and concentrated by chelation and extraction. Three organic solvents (methyl isobutyl ketone, di-isobutyl ketone and isoamyl alcohol) and two ligands (8-hydroxyquinoline and toluene-3,4-dithiol) were studied. The procedure were tested on pine needle and birch leaf samples.

  18. Determination of nickel in biological materials after microwave dissolution using inductively coupled plasma atomic emission spectrometry with prior extraction into butan-1-ol.

    PubMed

    Vereda Alonso, E; García de Torres, A; Cano Pavón, J M

    1992-07-01

    A sensitive procedure has been developed for the determination of ultratrace amounts of nickel in biological materials by inductively coupled plasma atomic emission spectrometry after extraction of the nickel ion into butan-1-ol by using 1,5-bis(di-2-pyridylmethylene)thiocarbonohydrazide as the extracting reagent. Fast, efficient and complete sample digestion is achieved by an HNO3-HCl poly(tetrafluoroethylene) bomb dissolution technique using microwave heating. Results obtained for eleven certified reference materials agreed with the certified values.

  19. Hyphenated techniques in speciation analysis of polyoxometalates: identification of individual [PMo12-xVxO40](-3-x) (x = 1-3) in the reaction mixtures by high performance liquid chromatography and atomic emission spectrometry with inductively coupled plasma.

    PubMed

    Shuvaeva, O V; Zhdanov, A A; Romanova, T E; Abramov, P A; Sokolov, M N

    2017-03-14

    Unambiguous identification of polyoxometalate (POM) species generated in self-assembly reactions in solution is rather problematic due to close similarity of their properties such as solubility and spectral characteristics. The situation is made more complex by protonation equilibria (which can change their analytical signals) and the lack of individual compounds to serve as standards for individual members of these mixtures. In the present work a new approach to the study of such POMs has been suggested, taking molybdovanadates [PMo12-xVxO40](-3-x) as a model. The key feature of this approach consists of generation of so-called "conditional model systems" that include most of the expected components of a mixture formed by self-assembly, tracked down by reliable detection techniques, e.g., (51)V NMR-spectroscopy in this particular case. Then the proposed composition of the mixture is verified and corrected by means of high-performance liquid chromatography coupled with inductively coupled plasma atomic emission spectrometry (HPLC-ICP-AES).

  20. Purge-and-trap preconcentration system coupled to capillary gas chromatography with atomic emission detection for 2,4,6-trichloroanisole determination in cork stoppers and wines.

    PubMed

    Campillo, Natalia; Aguinaga, Nerea; Viñas, Pilar; López-García, Ignacio; Hernández-Córdoba, Manuel

    2004-12-17

    A method based on solvent extraction and purge-and-trap capillary gas chromatography with atomic emission detection (PT-GC-AED) for the determination of 2,4,6-trichloroanisole (TCA) in wines and cork stoppers was optimized and evaluated. TCA was previously extracted from the samples in pentane and the preconcentrated extract was reconstituted in water before being injected into the chromatograph by means of the PT system. Element-specific detection and quantification was carried out by monitoring the chlorine (479 nm) emission line. Two different calibration graphs were used to quantify TCA in the cork or the wine samples, owing to the interference produced by the ethanol content in the wines. Detection limits of 25 pg g(-1) and 5 ng l(-1) were obtained for corks and wines, respectively. The method provided recoveries from spiked samples ranging from 88.5 to 102.3%, confirming the reliability of the procedure and its suitability for routine monitoring.

  1. TiO2 in commercial sunscreen lotion: flow field-flow fractionation and ICP-AES together for size analysis.

    PubMed

    Contado, Catia; Pagnoni, Antonella

    2008-10-01

    A new method for determining the size of titanium dioxide particles is proposed and assayed in a commercial sunscreen product. Today many sun protection cosmetics incorporate physical UV filters as active ingredients, and there are no official methods for determining these compounds in sunscreen cosmetics. Here flow field-flow fractionation (FlFFF) has been tested, first to sort two different types of TiO2 nano- and microstandard materials (AeroxideTiO2 Degussa P-25 and TiO2 rutile 0.1-0.2-microm size) and then to fractionate TiO2 particles, extracted from a commercial sunscreen lotion. All the TiO2 FlFFF separations were detected by UV but during elution fractions were collected and their Ti content measured by inductively coupled plasma-atomic emission spectrometer (ICP-AES); the Ti concentration profiles obtained by ICP-AES were well correlated with the UV signals. The TiO2 particle mass-size distribution were calculated from the UV profiles. This methodology is relatively simple and rapid, and the sample treatment is as a whole easy and low cost.

  2. Geographical traceability of wild Boletus edulis based on data fusion of FT-MIR and ICP-AES coupled with data mining methods (SVM)

    NASA Astrophysics Data System (ADS)

    Li, Yun; Zhang, Ji; Li, Tao; Liu, Honggao; Li, Jieqing; Wang, Yuanzhong

    2017-04-01

    In this work, the data fusion strategy of Fourier transform mid infrared (FT-MIR) spectroscopy and inductively coupled plasma-atomic emission spectrometry (ICP-AES) was used in combination with Support Vector Machine (SVM) to determine the geographic origin of Boletus edulis collected from nine regions of Yunnan Province in China. Firstly, competitive adaptive reweighted sampling (CARS) was used for selecting an optimal combination of key wavenumbers of second derivative FT-MIR spectra, and thirteen elements were sorted with variable importance in projection (VIP) scores. Secondly, thirteen subsets of multi-elements with the best VIP score were generated and each subset was used to fuse with FT-MIR. Finally, the classification models were established by SVM, and the combination of parameter C and γ (gamma) of SVM models was calculated by the approaches of grid search (GS) and genetic algorithm (GA). The results showed that both GS-SVM and GA-SVM models achieved good performances based on the #9 subset and the prediction accuracy in calibration and validation sets of the two models were 81.40% and 90.91%, correspondingly. In conclusion, it indicated that the data fusion strategy of FT-MIR and ICP-AES coupled with the algorithm of SVM can be used as a reliable tool for accurate identification of B. edulis, and it can provide a useful way of thinking for the quality control of edible mushrooms.

  3. Geographical traceability of wild Boletus edulis based on data fusion of FT-MIR and ICP-AES coupled with data mining methods (SVM).

    PubMed

    Li, Yun; Zhang, Ji; Li, Tao; Liu, Honggao; Li, Jieqing; Wang, Yuanzhong

    2017-04-15

    In this work, the data fusion strategy of Fourier transform mid infrared (FT-MIR) spectroscopy and inductively coupled plasma-atomic emission spectrometry (ICP-AES) was used in combination with Support Vector Machine (SVM) to determine the geographic origin of Boletus edulis collected from nine regions of Yunnan Province in China. Firstly, competitive adaptive reweighted sampling (CARS) was used for selecting an optimal combination of key wavenumbers of second derivative FT-MIR spectra, and thirteen elements were sorted with variable importance in projection (VIP) scores. Secondly, thirteen subsets of multi-elements with the best VIP score were generated and each subset was used to fuse with FT-MIR. Finally, the classification models were established by SVM, and the combination of parameter C and γ (gamma) of SVM models was calculated by the approaches of grid search (GS) and genetic algorithm (GA). The results showed that both GS-SVM and GA-SVM models achieved good performances based on the #9 subset and the prediction accuracy in calibration and validation sets of the two models were 81.40% and 90.91%, correspondingly. In conclusion, it indicated that the data fusion strategy of FT-MIR and ICP-AES coupled with the algorithm of SVM can be used as a reliable tool for accurate identification of B. edulis, and it can provide a useful way of thinking for the quality control of edible mushrooms.

  4. Determination of non-metallic elements by capacitively coupled helium microwave plasma atomic emission spectrometry with capillary gas chromatography.

    PubMed

    Uchida, H; Berthod, A; Winefordner, J D

    1990-07-01

    A capacitively coupled microwave helium plasma with a tubular tantalum electrode was evaluated as an element selective detector for gas chromatography (GC). The end of a 10-m bonded fused capillary column was directly inserted into the tubular electrode without any switching system. A heated copper tube was used to house the part of the GC column that protruded from the oven. The optimisation of operating parameters, line selection, background emission and horizontal and vertical observation position is described. Analytical figures of merit including sensitivity, reproducibility, signal to background ratio, selectivity, dynamic range and limit of detection (LOD), were evaluated for carbon, hydrogen, chlorine and bromine emission. Limits of detection in the low ng range (20 pmol) were obtained for halogenated compounds using carbon emission, whereas LODs in the 0.1 micrograms range (2 nmol) were obtained using chlorine or bromine emission lines.

  5. Silicon microhole array prepared by ICP

    NASA Astrophysics Data System (ADS)

    Duanmu, Qingduo; Zhang, Anping; Wang, Guozheng; Gao, Yanjun; Li, Ye; Jiang, Delong; Fu, Lichen; Tian, Jingquan

    2004-12-01

    This paper reports on a silicon micro-hole arrays (Si-MHA) prepared by Inductively Coupled Plasma (ICP) etching, a dry etching method. By ICP etcher, we carried out several experimental researches and process exploration for micromachining Si-MHA. The mechanism of lateral etching, sidewall passivation, gas micro-transport and some process parameters in Si-MHA micromachining, such as gas switching time, flow rate, etching rate, were analyzed. The footing effect, lag effect, longitudinal strips and RIE grass effect occurred in the ICP etching process were also studied. These process problems had reappeared in the micro-hole arrays process though these problems had be solved in the field of integrated circuits process and microelectromechanical system (MEMS). The study results reported here had demonstrated a Si-MHA that the diameter was 15 μm, the center distance 30 μm, and the depth 240 μm prepared by ICP, and had led the author to believe that the deep pore structure and the deep trench with high aspect ratio were very different in etching process. The former is a closed structure for the gas transport, and the latter is an open structure, so the process of deep hole structure is a puzzle in micromachining and MEMS technology.

  6. Determination of thorium by ICP-MS and ICP-OES.

    PubMed

    Holmes, L

    2001-01-01

    Natural thorium (232-Th) has traditionally been measured by radiometric techniques such as alpha and gamma spectrometry. However. with both ICP-OES and ICP-MS instruments becoming relatively common in many analytical laboratories. these techniques have become more acceptable in thorium analysis. This paper will briefly describe an overview of the instrumentation currently available and the techniques themselves applied to thorium analysis. Both techniques have low detection limits and require little sample treatment after the sample digestion. Routine sample analysis time is short and spectra easy to interpret. usually giving results with low uncertainties, Whereas ICP-OES measures total thorium only, ICP-MS also offers the potential to measure other long-lived thorium isotopes (t 1/2 > 10(4) years), such as 232Th. However, other important isotopes, such as 228Th. are still out of reach for routine analysis. The main disadvantage of the techniques is the requirement for a sample digestion stage.

  7. Soft x-ray emission of galliumlike rare-earth atoms produced by high-temperature low-density tokamak and high-density laser plasmas

    SciTech Connect

    Fournier, K.B.; Goldstein, W.H.; Osterheld, A. ); Finkenthal, M.; Lippmann, S.; Huang, L.K.; Moos, H.W. ); Spector, N. )

    1994-09-01

    Spectra of rare-earth atoms praseodymium, [ital Z]=59, to ytterbium, [ital Z]=70, emitted from the high-temperature (1 keV) low-density (10[sup 13] cm[sup [minus]3]) TEXT tokamak (at the Fusion Research Center, University of Texas, Austin) and high-density (10[sup 20] cm[sup [minus]3]) laser plasmas have been recorded in the soft-x-ray range of 50--200 A with an image intensifier detector and on photographic plates. The brightest [ital n]=4 to [ital n]=4 transitions of galliumlike ions have been identified and their emission patterns have been studied by comparison with [ital ab] [ital initio] atomic structure calculations and collisional radiative models under the respective plasma conditions. We have investigated the use of the ratios of the intensities of 4-4 transitions as indicators of plasma densities. This is possible owing to the doublet structure of the galliumlike ground state, which leads to a strong density dependence for ratios of transitions between low-lying levels. We have also used semiempirical ionization balance calculations to characterize the charge state distribution of the tokamak plasmas, in preparation for an investigation of the use of ratios of galliumlike to zinclike and copperlike emission features as indicators of whether the impurities are in coronal equilibrium or undergoing ionization.

  8. Analytical capability of a medium power capacitively coupled plasma for the multielemental determination in multimineral/multivitamin preparations by atomic emission spectrometry.

    PubMed

    Frentiu, Tiberiu; Ponta, Michaela; Darvasi, Eugen; Frentiu, Maria; Cordos, Emil

    2012-10-15

    A method for multielemental (Ca, Cr, Cu, Fe, K, Mg, Mn, Na, P and Zn) determination in multimineral/multivitamins by atomic emission spectrometry in a medium power radiofrequency capacitively coupled plasma (275 W) and low Ar consumption (0.4 L min(-1)) is proposed. Determinations were performed on commercially available tablets and a standard reference material after acidic high-pressure microwave assisted digestion and using the standard additions procedure. The detection limits (mg g(-1)) were in the range 0.003 (Na)-1.5 (P) and were not depreciated by the non-spectral interference of mineral matrices of K, Ca, Mg and Na excepting Zn and P. Found concentrations corresponded generally to the labelled contents with recovery in the range of 90-107% and 1.0-13.0% repeatability. The proposed technique could be an advantageous alternative to the more expensive inductively coupled plasma atomic emission spectrometry in the quality control of multimineral/multivitamin preparations. Copyright © 2012 Elsevier Ltd. All rights reserved.

  9. Coherently controlled emissions |4P3/2,1/2> ↔ |4S1/2> from a femtosecond Λ-type excitation scheme in potassium atom

    NASA Astrophysics Data System (ADS)

    Pentaris, D.; Damianos, D.; Papademetriou, G.; Lyras, A.; Steponkevičius, K.; Vaičaitis, V.; Efthimiopoulos, T.

    2016-07-01

    The combined excitation of high density potassium (K) vapour by 100 fs pump-coupling pulses is experimentally studied. The intense pump pulse excites the two-photon ? transition and internally generated emissions are initiated along the atomic paths: ? (path-1) and, ? (path-2). The temporally delayed coupling pulse coherently drives the ? transitions, in a Λ-type excitation scheme. The competing axial and conical emission components of the well-resolved ? transitions (D2 and D1 lines of K) are substantially enhanced and controlled, for appropriate detunings and pump-coupling temporal delays. The coherence relaxation time (CRT) of the two-photon excited ? state is determined by exploiting the temporal delay in the pulse sequence. The effect of the pulse delay and the fs pulse bandwidth on the system dynamics is discussed as well as the role of dephasing collisions between K and buffer gas atoms. The proposed scheme can be employed in radiative multi-level systems, for the direct estimation of coherence relaxation rates of various states.

  10. Emissions enhancement in a pump-coupling V-type coherently controlled four-level atomic system

    NASA Astrophysics Data System (ADS)

    Pentaris, D.; Papademetriou, G.; Efthimiopoulos, T.; Merlemis, N.; Lyras, A.

    2013-12-01

    The nonlinear interaction of a four-level potassium system with a strong pump and a weak coupling laser is investigated. A strong pump pulse excites the two-photon transition ?, causing prompt parametric emissions along the path-1 ? and delayed emissions in the second available de-excitation path-2 ?. A weak coupling pulse is introduced to coherently excite either the transition ? (path-1) or the ? one (path-2) in a V-type scheme. Results are presented for the emissions generated under the combined action of the pump-coupling pulses as a function of their delay for certain peak pulse intensities and coherence relaxation times (CRTs) related to dephasing collisions. We find that emissions in path-1 are considerably enhanced for negative delays (counterintuitive pulse sequence) of the order of the CRT. An approach is suggested for the estimation of CRTs. Emissions in path-2 are enhanced and temporally shifted, suggesting an approach to control this path by varying the pulse delay.

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

    PubMed

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

    2005-01-01

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

  12. Optoelectronic properties of Black-Silicon generated through inductively coupled plasma (ICP) processing for crystalline silicon solar cells

    NASA Astrophysics Data System (ADS)

    Hirsch, Jens; Gaudig, Maria; Bernhard, Norbert; Lausch, Dominik

    2016-06-01

    The optoelectronic properties of maskless inductively coupled plasma (ICP) generated black silicon through SF6 and O2 are analyzed by using reflection measurements, scanning electron microscopy (SEM) and quasi steady state photoconductivity (QSSPC). The results are discussed and compared to capacitively coupled plasma (CCP) and industrial standard wet chemical textures. The ICP process forms parabolic like surface structures in a scale of 500 nm. This surface structure reduces the average hemispherical reflection between 300 and 1120 nm up to 8%. Additionally, the ICP texture shows a weak increase of the hemispherical reflection under tilted angles of incidence up to 60°. Furthermore, we report that the ICP process is independent of the crystal orientation and the surface roughness. This allows the texturing of monocrystalline, multicrystalline and kerf-less wafers using the same parameter set. The ICP generation of black silicon does not apply a self-bias on the silicon sample. Therefore, the silicon sample is exposed to a reduced ion bombardment, which reduces the plasma induced surface damage. This leads to an enhancement of the effective charge carrier lifetime up to 2.5 ms at 1015 cm-3 minority carrier density (MCD) after an atomic layer deposition (ALD) with Al2O3. Since excellent etch results were obtained already after 4 min process time, we conclude that the ICP generation of black silicon is a promising technique to substitute the industrial state of the art wet chemical textures in the solar cell mass production.

  13. Elemental bioimaging by means of LA-ICP-OES: investigation of the calcium, sodium and potassium distribution in tobacco plant stems and leaf petioles.

    PubMed

    Thyssen, G M; Holtkamp, M; Kaulfürst-Soboll, H; Wehe, C A; Sperling, M; von Schaewen, A; Karst, U

    2017-06-21

    Laser ablation-inductively coupled plasma-optical emission spectroscopy (LA-ICP-OES) is presented as a valuable tool for elemental bioimaging of alkali and earth alkali elements in plants. Whereas LA-ICP-OES is commonly used for micro analysis of solid samples, laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) has advanced to the gold standard for bioimaging. However, especially for easily excitable and ubiquitous elements such as alkali and earth alkali elements, LA-ICP-OES holds some advantages regarding simultaneous detection, costs, contamination, and user-friendliness. This is demonstrated by determining the calcium, sodium and potassium distribution in tobacco plant stem and leaf petiole tissues. A quantification of the calcium contents in a concentration range up to 1000 μg g(-1) using matrix-matched standards is presented as well. The method is directly compared to a LA-ICP-MS approach by analyzing parallel slices of the same samples.

  14. A new electron spectroscopy system for measuring electron emission from fast ion interactions with atomic, molecular, and condensed phase targets

    NASA Astrophysics Data System (ADS)

    Hawkins, Wilson L.

    A new electron spectroscopy system has been developed for measuring electron emission from gas and solid targets induced by fast ion impact. This system uses an ultrahigh-vacuum compatible cylindrical deflector analyzer, designed and fabricated in the Department of Physics at East Carolina University, to measure electron yields as a function of electron energy and emission angle for fast ions interacting with materials. The new spectroscopy system was tested in a previously existing high-vacuum target chamber that has been installed on a new beam line in the ECU Accelerator Laboratory. In addition to the new analyzer, a new data acquisition and experimental control system, based on LabVIEW computer control software, was developed and tested using an existing cylindrical mirror analyzer. Data from this system was compared to previous results to confirm the functionality of the design. Subsequently, the new analyzer was installed in the high-vacuum target chamber and tested by measuring Auger electron emission from 2 MeV protons incident on an argon gas target and comparing to well-known emission spectra. Ultimately, the new electron spectroscopy system will be used for measuring electron yields from condensed phase targets in ultrahigh-vacuum conditions in future experiments.

  15. Some aspects of pulsed laser deposited nanocrystalline LaB(6) film: atomic force microscopy, constant force current imaging and field emission investigations.

    PubMed

    Late, Dattatray J; Date, Kalyani S; More, Mahendra A; Misra, Pankaj; Singh, B N; Kukreja, Lalit M; Dharmadhikari, C V; Joag, Dilip S

    2008-07-02

    Nanocrystalline lanthanum hexaboride (LaB(6)) films have been deposited on molybdenum foil by the pulsed laser deposition (PLD) technique. The as-deposited films were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The XRD pattern shows the cubic crystallinity of the LaB(6) film. The AFM studies reveal that the conical shaped LaB(6) nanostructures have height 60 nm, base 800 nm, and a typical radius of curvature ∼20 nm. A comparison of force and in situ current imaging AFM studies reveals that current contrast does not originate from the surface topography of the LaB(6) film. Field emission studies have been performed in the planar diode configuration. A current density of 4.4 × 10(-2) A cm(-2) is drawn from the actual emitting area. The Fowler-Nordheim plot is found to be linear, in accordance with the quantum mechanical tunneling phenomenon. The field enhancement factor is estimated to be 3585, indicating that the field emission is from LaB(6) nanocrystallites present on the emitter surface, as confirmed by the AFM. The emission current-time plots show current stability to the extent of 5% fluctuation about the average current over a period of 3 h.

  16. Atomic layer deposition of TiO2 and Al2O3 on nanographite films: structure and field emission properties

    NASA Astrophysics Data System (ADS)

    Kleshch, Victor I.; Ismagilov, Rinat R.; Smolnikova, Elena A.; Obraztsova, Ekaterina A.; Tuyakova, Feruza; Obraztsov, Alexander N.

    2016-03-01

    Atomic layer deposition (ALD) of metal oxides (MO) was used to modify the properties of nanographite (NG) films produced by direct current plasma-enhanced chemical vapor deposition technique. NG films consist of a few layers of graphene flakes (nanowalls) and nanoscrolls homogeneously distributed over a silicon substrate with a predominantly vertical orientation of graphene sheets to the substrate surface. TiO2 and Al2O3 layers, with thicknesses in the range of 50 to 250 nm, were deposited on NG films by ALD. The obtained NG-MO composite materials were characterized by scanning electron microscopy, energy dispersive x-ray analysis, and Raman spectroscopy. It was found that ALD forms a uniform coating on graphene flakes, while on the surface of needle-like nanoscrolls it forms spherical nanoparticles. Field emission properties of the films were measured in a flat vacuum diode configuration. Analysis based on obtained current-voltage characteristics and electrostatic calculations show that emission from NG-TiO2 films is determined by the nanoscrolls protruding from the TiO2 coverage. The TiO2 layers with thicknesses of <200 nm almost do not affect the overall field emission characteristics of the films. At the same time, these layers are able to stabilize the NG films' surface and can lead to an improvement of the NG cold cathode performance in vacuum electronics.

  17. Morphological characterization of cardiac induced intracranial pressure (ICP) waves in patients with overdrainage of cerebrospinal fluid and negative ICP.

    PubMed

    Eide, Per Kristian; Sroka, Marek; Wozniak, Aleksandra; Sæhle, Terje

    2012-10-01

    Symptomatic overdrainage of cerebrospinal fluid (CSF) can be seen in shunted hydrocephalus patients and in non-shunted patients with spontaneous intracranial hypotension (SIH). In these patients, intracranial pressure (ICP) monitoring often reveals negative static ICP, while it is less understood how the pulsatile ICP (cardiac induced ICP waves) is affected. This latter aspect is addressed in the present study. A set of 40 ICP recordings from paediatric and adult hydrocephalus patients were randomly selected. Each cardiac induced ICP wave was automatically identified and manually verified by the beginning and ending diastolic minimum pressures and the systolic maximum pressure. The ICP wave parameters (static pressure, amplitude, rise time, rise time coefficient, downward coefficient, wave duration, and area-under-curve) were then automatically computed. The material of 40 ICP recordings provided a total of 3,192,166 cardiac induced ICP waves (1,292,522 in paediatric patients and 1,899,644 in adult patients). No apparent changes in ICP wave parameters were seen when mean ICP became negative, except that the parameters amplitude, rise time coefficient, downward coefficient and area under curve somewhat increased when mean ICP was below -15 mmHg.

  18. Isotopic ratio measurements with ICP-MS

    SciTech Connect

    Russ, G.P. III; Bazan, J.M.

    1986-06-03

    An inductively-coupled-plasma source mass spectrometer (ICP-MS) has been used to measure the isotopic composition of U, Pb, Os, and B standards. Particular emphasis has been placed on uranium because of its nuclear and environmental interest and because of the availability of a well-characterized set of standards with a wide range of isotopic compositions. The precision and accuracy obtainable in isotope ratio measurements by ICP-MS depend on many factors including background, interferences, dead time, mass fractionation (bias), abundance sensitivity, and counting statistics. Which, if any, of these factors controls accuracy and precision depends on the type of sample being analyzed and the characteristics of the mass spectrometer. These issues are discussed in detail.

  19. Challenges in the quality assurance of elemental and isotopic analyses in the nuclear domain benefitting from high resolution ICP-OES and sector field ICP-MS.

    PubMed

    Krachler, Michael; Alvarez-Sarandes, Rafael; Van Winckel, Stefaan

    Accurate analytical data reinforces fundamentally the meaningfulness of nuclear fuel performance assessments and nuclear waste characterization. Regularly lacking matrix-matched certified reference materials, quality assurance of elemental and isotopic analysis of nuclear materials remains a challenging endeavour. In this context, this review highlights various dedicated experimental approaches envisaged at the European Commission-Joint Research Centre-Institute for Transuranium Elements to overcome this limitation, mainly focussing on the use of high resolution-inductively coupled plasma-optical emission spectrometry (HR-ICP-OES) and sector field-inductively coupled plasma-mass spectrometry (SF-ICP-MS). However, also α- and γ-spectrometry are included here to help characterise extensively the investigated actinide solutions for their actual concentration, potential impurities and isotopic purity.

  20. ICP Corporate Customer Assessment - Sampling Plan

    DTIC Science & Technology

    1995-07-01

    customers . Some activities identified by MRO files do not meet this definition. Shipments from DLA depots may be in response to requisitions for items managed ...for distribution customers actually accrues to the agency managing the items ordered; if not carefully manipulated, quantity and cost information on...requisitioning multiple commodities will appear in more than one cell. This method ensures visibility of customers to management at each ICP, as

  1. Characterization of helium/argon working gas systems in a radiofrequency glow discharge atomic emission source. Part II: Langmuir probe and emission intensity studies for Al, Cu and Macor samples

    NASA Astrophysics Data System (ADS)

    Belkin, Mikhail; Caruso, Joseph A.; Christopher, Steven J.; Marcus, R. Kenneth

    1998-08-01

    The application of a tuned Langmuir probe is extended to the measurement of the charged particle characteristics (electron and ion number density, average electron energy and electron temperature) in an analytical radiofrequency glow discharge (RF-GD) in helium. The effects of discharge operating conditions, such as RF power and pressure, on the charged particle characteristics for conducting (aluminum) and nonconducting (Macor) samples are studied. The differences in plasma characteristics between argon and helium working gases are discussed. Langmuir probe measurements are also performed in an argon/helium mixture. Variations of the emission intensities of sputtered analytes (copper and aluminum) are investigated when helium is introduced into an argon RF glow discharge plasma. It is recognized that, although the number of sample atoms in the plasma gradually decreases due to reduced sputtering, the emission intensities of various Al(I) and Cu(I) lines increase with helium addition. Measured electron and ion number densities also decrease with helium addition, whereas the average electron energy and electron temperature increase, accounting for the enhancement of emission intensities.

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

    USGS Publications Warehouse

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

    1982-01-01

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

  3. Methyl sulfonyl polychlorinated biphenyls and 2,2-bis(4-chlorophenyl)-1,1-dichlorethene in gray seal tissues determined by gas chromatography with electron capture detection and atomic emission detection

    SciTech Connect

    Janak, K.; Becker, G.; Colmisjoe, A.; Oestman, C.; Athanasiadou, M.; Valters, K.; Bergman, A.

    1998-06-01

    The presence of 24 methyl sulfonyl polychlorinated biphenyl (PCB) congeners (MeSO{sub 2}-CBs) and 3-methyl sulfonyl 2,2-bis(4-chlorophenyl)-1,1-dichlorethene (DDE) (MeSO{sub 2}-DDE), metabolites of PCB and DDE, in blubber, lung, and liver of gray seals has been determined by using atomic emission detection (AED) and electron capture detection (ECD). Selective accumulation of aryl methyl sulfones in blubber, liver, and lung tissue was also investigated. For the liver samples, a substantial and highly specific retention of PCB methyl sulfones was observed. The atomic emission technique significantly improved the determination of measured solutes compared with ECD. Atomic emission detection was also valuable for the monitoring of the prefractionation and to decrease the requirements of sample clean-up. Comparing both detection techniques showed a good correlation between the results of the AED sulfur-selective line and ECD.

  4. Modes competition in superradiant emission from an inverted sub-wavelength thick slab of two-level atoms

    NASA Astrophysics Data System (ADS)

    Manassah, Jamal T.

    2016-08-01

    Using the expansion in the eigenmodes of 1-D Lienard-Wiechert kernel, the temporal and spectral profiles of the radiation emitted by a fully inverted collection of two-level atoms in a sub-wavelength slab geometry are computed. The initial number of amplifying modes determine the specific regime of radiation. In particular, the temporal profile of the field intensity is oscillatory and the spectral profile is non-Lorentzian with two unequal height peaks in a narrow band centered at the slab thickness value at which the real parts of the lowest order odd and even eigenvalues are equal.

  5. [Standard addition determination of impurities in Na2CrO4 by ICP-AES].

    PubMed

    Wang, Li-ping; Feng, Hai-tao; Dong, Ya-ping; Peng, Jiao-yu; Li, Wu; Shi, Hai-qin; Wang, Yong

    2015-02-01

    Coupled plasma atomic emission spectrometry (ICP-AES) was used to determine the trace impurities of Ca, Mg, Al, Fe and Si in industrial sodium chromate. Wavelengths of 167.079, 393.366, 259.940, 279.533 and 251.611 nm were selected as analytical lines for the determination of Al, Ca, Fe, Mg and Si, respectively. The analytical errors can be eliminated by adjusting the determined solution with high pure hydrochloric acid. Standard addition method was used to eliminate matrix effects. The linear correlation, detection limit, precision and recovery for the concerned trace impurities have been examined. The effect of standard addition method on the accuracy for the determination under the selected analytical lines has been studied in detail. The results show that the linear correlations of standard curves were very good (R2 = 0.9988 to 0.9996) under the determined conditions. Detection limits of these trace impurities were in the range of 0.0134 to 0.0280 mg x L(-1). Sample recoveries were within 97.30% to 107.50%, and relative standard deviations were lower than 5.86% for eleven repeated determinations. The detection limits and accuracies established by the experiment can meet the analytical requirements and the analytic procedure was used to determine trace impurities in sodium chromate by ion membrane electrolysis technique successfully. Due to sodium chromate can be changed into sodium dichromate and chromic acid by adding acids, the established method can be further used to monitor trace impurities in these compounds or other hexavalent chromium compounds.

  6. [Determination of nano-silver spatiotemporal distribution in cut gerbera flowers by ICP-AES].

    PubMed

    Lü, Pei-Tao; Huang, Xin-Min; Lu, Yi-Min; Liu, Ji-Ping; Zhang, Zhao-Qi; He, Sheng-Gen

    2011-08-01

    The spatiotemporal distribution of nano-silver in cut gerbera (Gerbera hybrida cv. Crossfire) flowers were determined by inductively coupled plasma-atomic emission spectrometry technique (ICP-AES). The relative standard deviations of this method were between 0.14% and 2.89%, and the recovery ratio obtained by standard addition method ranged from 93.33% to 106.67%. The method was proved to be simple, rapid, reliable and highly sensitive, which can meet the demands of actual sample analysis. The experimental results also showed that Ag could be found in the basal stem end, upper stem end and petal of the cut gerbera flowers treated in nano-silver solution of 5 mg x L(-1) for 24 h and thereafter placed in distilled water. However, the Ag content in basal stem ends was much higher than those in upper stem ends and petals. The results indicated that nano-silver particles could enter into the flower stems through the cuts of stem ends and then moved to different parts of the cut gerbera flowers, but most of them located in the basal stem ends during the vase period. The fact that Ag was centred in basal stem end implied that the positive preservation effects of nano-silver on cut gerbera flowers is related to its strong and sustainable antiseptic action in the stem ends of cut flowers. The above results provide a reliable method for the determination of nano-silver and theoretical basis for its futher research and application in the preservation of cut flowers.

  7. Electrothermal atomization atomic absorption spectrometry for the determination of lead in urine: results of an interlaboratory study

    NASA Astrophysics Data System (ADS)

    Parsons, Patrick J.; Slavin, Walter

    1999-05-01

    Results of an interlaboratory study are reported for the determination of lead in urine. Two levels of a lyophilized material containing biologically-bound lead were prepared using pooled urine obtained from lead-poisoned children undergoing the CaNa 2EDTA mobilization test. The materials were circulated to a group of reference laboratories that participate in the `New York State Proficiency Testing Program for Blood Lead'. Results of the initial round-robin gave all-method consensus target values of 145±22 μg/l (S.D.) for lot 17 and 449±43 μg/l (S.D.) for lot 20. The interlaboratory exercise was repeated some 5 years later and consensus target values were re-calculated using the grand mean (excluding outliers) of results reported by laboratories using electrothermal atomization atomic absorption spectrometry (ETAAS). The re-calculated target values were 139±10 μg/l (S.D.) and 433±12 μg/l (S.D.). The urine reference materials were also analyzed for lead by several laboratories using other instrumental techniques including isotope dilution (ID), inductively coupled plasma (ICP) mass spectrometry (MS), flame atomic absorption with extraction, ICP-atomic emission spectrometry, ID-gas chromatography MS and flow injection-hydride generation AAS, thus providing a rich source of analytical data with which to characterize them. The materials were also used in a long-term validation study of an ETAAS method developed originally for blood lead determinations that has since been used unmodified for the determination of lead in urine also. Recently, urine lead method performance has been tracked in a proficiency testing program specifically for this analysis. In addition, a number of commercial control materials have been analyzed and evaluated.

  8. Determination of heavy metal pollution with environmental physicochemical parameters in waste water of Kocabas Stream (Biga, Canakkale, Turkey) by ICP-AES.

    PubMed

    Yayintas, Ozlem Tonguc; Yilmaz, Selahattin; Turkoglu, Muhammet; Dilgin, Yusuf

    2007-04-01

    Waste water pollution of industrial areas can answer for the serious consequences of one of the most important environmental threats to the future. In this study, inductively coupled plasma-atomic emission spectrometry method (ICP-AES) is proposed to determine heavy metals (Pb, Cu, Cd, Cr, Zn, Al, Fe, Ni, Co, Mn) and major elements (Ca, Mg) in waste water of Kocabas Stream. The concentration of metals in the waste water samples taken from 9 different stations (St.) in Biga-Kocabas Stream in November 2004 (autumn period) were determined after simple pretreatment of samples by the proposed ICP-AES method. An analysis of a given sample is completed in about 15 min for ICP-AES the method. The results of heavy metals concentrations in waste water were found between 0.00001-77.69610 mg l(-1) by the ICP-AES technique. The concentrations of Pb, Cd, Cu, Zn, Cr, Al, Fe, Mn, Ni, Co, Mg and Ca 0.00001 (St.3,6,7) - 0.0087 mg l(-1) (St.9), 0.00001 (St.4-7) - 0.0020 mg l(-1) (St.8), 0.00001 (St.1,3-7,9) - 0.0041 mg l(-1) (St.2), 0.0620 (St.2) - 0.2080 mg l(-1) (St.3), 0.0082 (St.6) - 0.2290 mg l(-1) (St.8), 0.3580 (St.2) - 1.7400 mg l(-1) (St.3), 0.2240 (St.1) - 0.6790 mg l(-1) (St.3), 0.0080 (St.1) - 1.5840 mg l(-1) (St.3), 0.0170 (St.3) - 0.0640 mg l(-1) (St.2), 0.0010 (St.1,4,5,8) - 0.0080 mg l(-1) (St.3), 5.0640 (St.9) - 5.2140 mg l(-1) (St.1) and 43.3600 (St.2) - 77.6961 mg l(-1) (St.9), respectively. Also we measured environmental physicochemical parameters such as temperature, salinity, specific conductivity, total dissolved solid (TDS), pH, oxidation and reduction potential (ORP), and dissolved oxygen (DO) in the waste water at sampling stations.

  9. Application of inductively coupled plasma atomic emission spectroscopy analysis with a polychromator/monochromator combination the byproducts of coal-fired power stations

    NASA Astrophysics Data System (ADS)

    Weers, C. A.

    The by-products of coal-fired power plants may be hazardous for the environment. Good analysis methods are therefore required in order to establish either a possible usage of the by-products or their possible storage. Preliminary experiments performed with inductively coupled plasma atomic emission spectroscopy have proven very successful. Moreover, the method is cost-effective. A short description is given of the optimized system for routine analysis. The system consists of a 2- and a 15-channel polychromator in combination with a monochromator. The opportunities is provides are also described. Use of the monochromator to analyze coal and run-off water from the flue-gases desulphurization, and of the polychromators to analyze coal fly-ash is described separately.

  10. [On-line determination of niobium and tantalum in soil and geochemical exploration samples by inductively coupled plasma atomic emission spectrometry with solvent extraction flow injection].

    PubMed

    Ai, J; Tang, Z Y

    2001-10-01

    A new method for the determination of trace niobium and tantalum in soil and geochemical exploration samples by inductively coupled plasma atomic emission spectrometry with solvent extraction flow injection was proposed. The niobium and tantalum were extracted with the mixed solvent of MIBK and TBP at 1 mol.L-1 HF and 4 mol.L-1 H2SO4. Experiment conditions and manifold parameters were investigated in detail. The detection limits were 0.5 x 10(-12) g.L-1 and 0.8 x 10(-12) g.L-1. The proposed method was rapid, simple and accurate, it has been applied to the determination of trace niobium and tantalum in national standard samples. The results were in good agreement with certified values with precisions of 4.5% and 5.1% RSD (n = 10). The sample throughput for niobium and tantalum is 20.h-1.

  11. Simultaneous determination of chlorinated organic compounds from environmental samples using gas chromatography coupled with a micro electron capture detector and micro-plasma atomic emission detector

    NASA Astrophysics Data System (ADS)

    Quan, Xie; Chen, Shuo; Platzer, Bernhard; Chen, Jingwen; Gfrerer, Marion

    2002-01-01

    Water and sediment samples were screened simultaneously for the presence of polychlorinated organic compounds using gas chromatography (GC) coupled with an micro electron capture detector (μ-ECD) and a newly developed helium plasma based on a micro-atomic emission detector (μ-AED). The GC column effluent was split 15:85 between two detectors. In this way, two chromatograms, one obtained by μ-ECD and another by μ-AED, were recorded simultaneously. α-, β-hexachlorocyclohexane and p, p'-DDE were detected. RSDs of the monitoring results from the two detection methods were <20% for the three compounds. A detection limit of 8.5 pg and at least 3 orders of magnitude of linear range for μ-AED was observed.

  12. Laser based analysis using a passively Q-switched laser employing analysis electronics and a means for detecting atomic optical emission of the laser media

    DOEpatents

    Woodruff, Steven D.; Mcintyre, Dustin L.

    2016-03-29

    A device for Laser based Analysis using a Passively Q-Switched Laser comprising an optical pumping source optically connected to a laser media. The laser media and a Q-switch are positioned between and optically connected to a high reflectivity mirror (HR) and an output coupler (OC) along an optical axis. The output coupler (OC) is optically connected to the output lens along the optical axis. A means for detecting atomic optical emission comprises a filter and a light detector. The optical filter is optically connected to the laser media and the optical detector. A control system is connected to the optical detector and the analysis electronics. The analysis electronics are optically connected to the output lens. The detection of the large scale laser output production triggers the control system to initiate the precise timing and data collection from the detector and analysis.

  13. Application of ICP-OES for Evaluating Energy Extraction and Production Wastewater Discharge Impacts on Surface Waters in Western Pennsylvania

    EPA Science Inventory

    Oil and gas extraction and coal-fired electrical power generating stations produce wastewaters that are treated and discharged to rivers in Western Pennsylvania with public drinking water system (PDWS) intakes. Inductively coupled plasma optical emission spectroscopy (ICP-OES) w...

  14. Application of ICP-OES for Evaluating Energy Extraction and Production Wastewater Discharge Impacts on Surface Waters in Western Pennsylvania

    EPA Science Inventory

    Oil and gas extraction and coal-fired electrical power generating stations produce wastewaters that are treated and discharged to rivers in Western Pennsylvania with public drinking water system (PDWS) intakes. Inductively coupled plasma optical emission spectroscopy (ICP-OES) w...

  15. Stable and high-quality Al-doped ZnO films with ICP-assisted facing targets sputtering at low temperature

    NASA Astrophysics Data System (ADS)

    Choi, Yoon S.; Kim, Hye R.; Han, Jeon G.

    2014-04-01

    FTS (facing targets sputtering) has been studied intensively for high-quality TCO films in low-temperature processes. In this study, we designed ICP-assisted FTS process for high-quality Al-doped ZnO film synthesis in a low temperature process. A one-turn ICP coil was installed a few cm above the upper target edge through which hydrogen was introduced and fully dissociated to the atomic radicals. The increase of ICP power caused heating and rarefaction of Ar gas and generated abundant hydrogen atoms and hydrogenated molecules. In FESEM analysis, the films synthesized with high ICP power showed high crystallinity. XPS was used to analyze the film structure. In O1s spectra, the low binding energy component located at ˜530.3 ± 0.4 eV corresponding to O2- ions on the wurtzite structure of the hexagonal Zn2+ ion array increased with the ICP power, indicating good crystal quality. With increasing ICP power fixing while fixing the RF power at the cathode, the resistivity was observed to decrease to 5 × 10-4 Ω-cm. For thermal reliability tests, films were stored in an air-based chamber at 200 °C. The films synthesized without ICP showed rapid degradation in the electrical properties, while the films synthesized with high ICP power showed good stabilities with little change in the electrical properties after 30 h of storage in an oven. By adding hydrogen, the carrier concentration of the films increased, while the mobility did not change much. From these results, it is expected that hydrogen was incorporated into the film as a stable n-dopant by using an auxiliary ICP plasma source.

  16. Traceable phosphorus measurements by ICP-OES and HPLC for the quantitation of DNA.

    PubMed

    Holden, Marcia J; Rabb, Savelas A; Tewari, Yadu B; Winchester, Michael R

    2007-02-15

    Measurement of the phosphorus content of nucleotides and deoxyribonucleic acid (DNA) offers an approach to the quantitation of nucleic acids that is traceable to the SI. Such measurements can be an alternative to the commonly used spectroscopic tools that are not traceable. Phosphorus measurements of thymidine 5'-monophosphate (TMP) and acid-digested plasmid and genomic DNA preparations were made using high-performance inductively coupled plasma optical emission spectroscopy (HP-ICP-OES) and high-performance liquid chromatography (HPLC) and compared for bias and uncertainty. A prerequisite for quality measurement is the purity of the materials. Quantitation with the two platforms was comparable for the TMP. However, the HPLC values had larger uncertainties and were all statistically different from the gravimetric values at the 95% confidence level. When using ICP-OES, the digestion of the nucleotide monophosphate can be eliminated, thus simplifying the procedure. The differences between the results obtained by using the two platforms, when measuring genomic or plasmid DNA, were dependent on the mass fraction of the digest. ICP-OES measurement of phosphorus provides a highly accurate quantitation for both nucleotide monophosphates and DNA with expanded uncertainties of less than 0.1%. Currently, ICP-OES requires a significant sample size restricting its usefulness for the quantitation of DNA but represents a valuable tool for certification of reference materials. HPLC requires smaller amounts of material to perform the analysis but is less useful for certification of reference materials because of lower accuracy and 10-fold higher expanded uncertainties.

  17. Method of low tantalum amounts determination in niobium and its compounds by ICP-OES technique.

    PubMed

    Smolik, Marek; Turkowska, Magdalena

    2013-10-15

    A method of determination of low amounts of tantalum in niobium and niobium compounds without its prior separation by means of inductively coupled plasma optical emission spectrometry (ICP-OES) has been worked out. The method involves dissolution of the analyzed samples of niobium as well as its various compounds (oxides, fluorides, chlorides, niobates(V)) in fluoride environments, precipitation of sparingly soluble niobic(tantalic) acid (Nb2O5(Ta2O5) · xH2O), converting them into soluble complex compounds by means of oxalic acid with addition of hydrogen peroxide and finally analyzing directly obtained solutions by ICP-OES. This method permits determination of Ta in niobium at the level of 10(-3)% with relatively good precision (≤ 8% RSD) and accuracy (recovery factor: 0.9-1.1). Relative differences in the results obtained by two independent methods (ICP-OES and ICP-MS) do not exceed 14%, and other elements present in niobium compounds (Ti, W, Zr, Hf, V, Mo, Fe, Cr) at the level of 10(-2)% do not affect determination. © 2013 Elsevier B.V. All rights reserved.

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

    PubMed

    Wagatsuma, Kazuaki

    2009-04-01

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

  19. Infrared (1-12 Micrometers) Atomic and Molecular Emission Signatures from Energetic Materials using Laser Induced Breakdown Spectroscopy

    DTIC Science & Technology

    2013-01-01

    chlorate and nitrate compounds including KClO3, NaClO3, KNO3, and NaNO3 to produce intense plasma at the target surface. IR LIBS studies on...molecular LIBS signatures from chlorate and nitrate compounds were observed at ~10 um and ~7.3 um, respectively. The observed molecular emissions showed... chlorate and nitrate compounds including KClO3, NaClO3, KNO3, and NaNO3 to produce intense plasma at the target surface. IR LIBS studies on

  20. Thermospheric atomic oxygen concentrations from WINDII O+(2P→2D) 732 nm emission: Comparisons with the NRLMSISE-00 and C-IAM models and with GUVI observations

    NASA Astrophysics Data System (ADS)

    Shepherd, Gordon G.; Cho, Young-Min; Fomichev, Victor I.; Martynenko, Oleg V.

    2016-09-01

    Thermospheric atomic oxygen concentrations have been retrieved from observations by the Wind Imaging Interferometer (WINDII) O+(2P→2D) 732 and 733 nm emissions and are compared with results obtained by the Global Ultraviolet Imager (GUVI). Although the observations compared were taken ten years apart, the periods were selected on the basis of solar activity, using the Canadian Ionosphere and Atmosphere Model (C-IAM) to bridge the time gap. Results from all of these were compared with those from the Naval Research Laboratory Mass Spectrometer and Incoherent Scatter (NRLMSISE-00) model. Comparisons were made on the basis of F10.7 solar flux, day of year, local time, season, latitude and longitude. The WINDII local time variations showed enhanced values for the Northern spring season. Latitude and longitude plots showed smooth variations for NRLMSISE-00 and large variations for both WINDII and GUVI observations; in particular a depression in atomic oxygen concentration around 40 °S latitude and 100 °E longitude that is tentatively identified with a longitudinal wave 1 that does not propagate in local time but has an annual variation. The averaged values showed the WINDII values to be 0.75 that of NRLMSISE-00 compared with 0.80 for GUVI. Thus the WINDII values agreed with those of GUVI to within 6%, although taken 10 years apart.