Academic literature on the topic 'Flame atomic emission spectrometry'

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Journal articles on the topic "Flame atomic emission spectrometry"

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Jackson, Kenneth W., and Huancheng Qiao. "Atomic absorption, atomic emission, and flame emission spectrometry." Analytical Chemistry 64, no. 12 (June 15, 1992): 50–66. http://dx.doi.org/10.1021/ac00036a003.

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Holcombe, James A., and D. Christian Hassell. "Atomic absorption, atomic emission, and flame emission spectrometry." Analytical Chemistry 62, no. 12 (June 15, 1990): 169–84. http://dx.doi.org/10.1021/ac00211a015.

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Jackson, Kenneth W., and Guoru Chen. "Atomic Absorption, Atomic Emission, and Flame Emission Spectrometry." Analytical Chemistry 68, no. 12 (January 1996): 231–56. http://dx.doi.org/10.1021/a1960012l.

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Jackson, Kenneth W., and Shijun Lu. "Atomic Absorption, Atomic Emission, and Flame Emission Spectrometry." Analytical Chemistry 70, no. 12 (June 1998): 363–84. http://dx.doi.org/10.1021/a1980012g.

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Jackson, Kenneth W., and Tariq M. Mahmood. "Atomic Absorption, Atomic Emission, and Flame Emission Spectrometry." Analytical Chemistry 66, no. 12 (June 1994): 252–79. http://dx.doi.org/10.1021/ac00084a012.

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JACKSON, K. W., and S. LU. "ChemInform Abstract: Atomic Absorption, Atomic Emission, and Flame Emission Spectrometry." ChemInform 29, no. 34 (June 20, 2010): no. http://dx.doi.org/10.1002/chin.199834350.

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Holcombe, James A., and Dean A. Bass. "Atomic absorption, atomic fluorescence, and flame emission spectrometry." Analytical Chemistry 60, no. 12 (June 15, 1988): 226–52. http://dx.doi.org/10.1021/ac00163a017.

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Holcombe, James A., and Thomas M. Rettberg. "Atomic absorption, atomic fluorescence, and flame emission spectrometry." Analytical Chemistry 58, no. 5 (April 1986): 124–44. http://dx.doi.org/10.1021/ac00296a012.

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Calloway, Clifton P., and Bradley T. Jones. "Atomic absorption spectrometry with a flame emission source." Spectrochimica Acta Part B: Atomic Spectroscopy 49, no. 12-14 (October 1994): 1707–15. http://dx.doi.org/10.1016/0584-8547(94)80142-8.

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Messman, Jerry D., Norman E. Schmidt, Joe D. Parli, and Robert B. Green. "Laser-Enhanced Ionization of Refractory Elements in a Nitrous Oxide-Acetylene Flame." Applied Spectroscopy 39, no. 3 (May 1985): 504–7. http://dx.doi.org/10.1366/0003702854248746.

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Laser-enhanced ionization (LEI) spectrometry using a water-cooled electrode immersed directly in a nitrous oxide-acetylene flame has been examined for the determination of refractory elements. LEI detection limits for refractory elements in aqueous solution are comparable to or better than detection limits obtained by flame atomic absorption, plasma emission, and atomic fluorescence techniques. Only graphite furnace atomic absorption spectrometry exhibits superior detectability for certain refractory elements in aqueous solution over LEI spectrometry using a nitrous oxide-acetylene flame. The successful application of the nitrous oxide-acetylene flame now extends the applicability of LEI spectrometry to include most of the elements in the periodic table which can be determined by other common atomic spectrochemical techniques.
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Dissertations / Theses on the topic "Flame atomic emission spectrometry"

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Penteado, Ana Julia. "Estudo do efeito da n-acetilcisteína sobre a toxicidade induzida pelo lítio." Universidade Estadual do Oeste do Paraná, 2017. http://tede.unioeste.br/handle/tede/2958.

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Submitted by Rosangela Silva (rosangela.silva3@unioeste.br) on 2017-08-30T14:53:20Z No. of bitstreams: 2 Ana Julia Penteado.pdf: 1485037 bytes, checksum: 723d1b3bedb90392ef459d2a4cedeca8 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)
Made available in DSpace on 2017-08-30T14:53:20Z (GMT). No. of bitstreams: 2 Ana Julia Penteado.pdf: 1485037 bytes, checksum: 723d1b3bedb90392ef459d2a4cedeca8 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2017-02-07
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES
Lithium carbonate is the main drug used to treat bipolar disorder. This medicine has a narrow therapeutic range and is usually used in a chronic way by the patients, generating the need for therapeutic monitoring by means of plasma lithium quantification. In addition, records of toxic effects from chronic medical use reinforce the need for a tool that assists in the treatment. Thus, a reliable methodology for the quantification of lithium and a therapeutic adjuvant emerge as a means to improve the quality of life of the patient. In our work, we used the flame atomic absorption spectrometer to validate the method for quantification of lithium and the results were satisfactory, because they complied with the required criteria, assuring the reliability of the method. In order to find a therapeutic adjuvant, N-acetylcysteine (NAC) was studied for presenting important characteristics against the toxic effects caused by lithium. In our results lithium presented toxic effects mainly inducing oxidative stress, while the coadministration of NAC reversed this effect in the liver, kidney and brain organs. The use of NAC as a therapeutic adjuvant has been shown to be promising, however, further studies need to be performed to better understand this relationship.
O carbonato de lítio é o principal medicamento utilizado no tratamento do transtorno bipolar. Este medicamento possuí estreita faixa terapêutica e geralmente é utilizado de forma crônica pelos pacientes, gerando a necessidade da monitorização terapêutica por meio da quantificação plasmática de lítio. Além disso, os registros de efeitos tóxicos decorrentes do uso medicinal crônico remetem a necessidade de uma ferramenta que auxilie no tratamento. Desta forma, uma metodologia confiável para a quantificação de lítio e um adjuvante terapêutico surgem como meios de melhorar a qualidade de vida do paciente. Em nosso trabalho, utilizamos o espectrômetro de absorção atômica de chama para validar um método para quantificação de lítio e os resultados foram satisfatórios, pois cumpriram os critérios exigidos, assegurando a confiabilidade do método. Com foco em buscar um adjuvante terapêutico, a N-acetilcisteína (NAC) foi estudada por apresentar características importantes contra os efeitos tóxicos causados pelo lítio. Em nossos resultados o lítio apresentou efeitos tóxicos principalmente induzindo o estresse oxidativo, enquanto que a coadministração de NAC reverteu esse efeito nos órgãos fígado, rim e cérebro. O uso da NAC como adjuvante terapêutico mostrou ser promissor, porém, mais estudos precisam ser realizados para entender melhor essa relação.
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Chun, Ka-him, and 秦嘉謙. "Single-particle inductively coupled plasma atomic emission spectrometry." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/209488.

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Transient emission of a particle in inductively coupled plasma-atomic emission spectrometry (ICP-AES) depends on the fundamental processes of aerosol desolvation, particle vaporization and atomization, ionization, excitation and diffusion of the analyte. Ideally, the rate of the above processes can be determined from the evolution of the transient emission as the ion plume moves along the central channel of the ICP. However, the dimension of the ion plume is significantly smaller than the central channel. The signal-to-background and signal-to-noise ratios suffer when the entire channel is imaged. Deconvolution of the temporal profile is required to determine the emission intensity of the ion plume versus observation height. Small aperture can be used to locate the vertical emission position accurately, but the evolution of the plume emission is lost. In this study, a double-slit method has been developed to pin-point two vertical positions of an ion plume. An ion plume travelling along the ICP central channel produces two peaks in the temporal emission profile. The temporal evolution of emission intensity can be correlated to delineate the degree of particle vaporization at the two positions. The relative widths and separation of the two peaks in a double-peak can be used to determine the analyte diffusion rate and particle velocity in the ICP, respectively. An unicellular green algae, chlorella vulgaris, was used as the test particles. The average Mg content of the algae is equivalent to MgO particles of diameter of 265nm. The strong ionic emission at wavelength of 279.55nm was monitored using a ¼ -m monochromator equipped with a PMT detector. Method of curve fitting was used to filter out the noise with minimum distortion of the peak shape for accurate determination of peak height and peak width. The merits of curve fitting versus methods of smoothing such as moving average and Savitzky-Golay filtering will be discussed. All transient emissions from the algal cells were detected with sufficient signal-to-noise ratio using a single-slit setup with slit height of 1mm at observation height of 18 mm above the load coil and ICP forward power of 1400 W. However, using the double-slit setup, less than half of the expected double-peaks were observed. One of the peaks in the double-peak can be below the detection limit and the double-peak is lost. An innovative development of this study is that the relative sensitivity corresponding to the 2 slits can be varied to enhance the intensity of the weaker emission peak. The peak with insufficient signal-to-noise ratio for detection can be enhanced to a level above the limit of detection. The number of observed double-peaks in increased and the observed particles are more representative of the population. Two types of double-peaks are categorized according to the relative intensity of the first peak to the second peak. A computer model was used to estimate the intensity ratio of the two emission peaks at different observation position of the ICP. The experimental and theoretical ratios agree generally. The theoretical ratio also shows the bias in the population sampled by the double-slit setup.
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Wingerd, Mark A. "A multi-mode spectrometer for atomic emission spectrometry." Diss., Virginia Tech, 1990. http://hdl.handle.net/10919/37396.

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Adeeyinwo, Christina Eromowen. "Flow Injection Atomic Absorption Spectrometry : analytical characteristics of flame AAS." Thesis, Loughborough University, 1990. https://dspace.lboro.ac.uk/2134/32021.

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Flow Injection (FI) techniques for use with Atomic Absorption Spectrometry (AAS) have attracted considerable research interest for sample introduction and calibration strategies. The interest continues in on-line preconcentration and matrix modification which are carried out by the incorporation of liquid-liquid extraction, ion-exchange, immobilised reagents, gas/vapour generation and continuous precipitation-filtration devices into suitably designed manifolds. Indirect determination of inorganic anions and organic compounds is becoming routine by FI–flame AAS. The direct analysis of solid samples, which is a shortcoming of flame AAS, was recently carried out by on-line electrolytic dissolutions.
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Dean, John R. "Mechanisms in discrete sample introduction for atomic emission spectrometry." Thesis, Imperial College London, 1986. http://hdl.handle.net/10044/1/37991.

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Bysouth, Stephen R. "Standard and sample manipulation for calibration in flame atomic absorption spectrometry." Thesis, Loughborough University, 1988. https://dspace.lboro.ac.uk/2134/33128.

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This thesis describes a study of existing calibration methods and a comparison of them, with novel calibration and sample pre-treatment methods for flame atomic absorption spectrometry (FAAS) developed by the author. A comparison of commercially available curve fitting algorithms was carried out to show how concentration errors arise and vary, due to the use of different empirical models for the calibration curve. Novel online dilution manifolds were designed. Using flow injection and continuous flow techniques, different calibration procedures were developed to allow null methods of calibration to be used and to extend the calibration range. Methods of sample pre-treatment were developed, including online dissolution and species separation, using flow injection analysis techniques. Members of the atomic spectroscopy group of the Royal Society of Chemistry were surveyed to discover calibration practices used in commercial laboratories. Respondents were asked questions on sample type, treatment and presentation, and data reduction for calibration. During the research, several papers were published and lectures given on the topics described.
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Carpenter, Robert Christopher. "Inductively coupled plasma-optical emission spectrometry for forensic analysis." Thesis, University of Plymouth, 1985. http://hdl.handle.net/10026.1/2680.

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The fundamental characteristics and applications of inductively coupled plasma - optical emission spectrometry (ICP-OES) for forensic science purposes have been evaluated. Optimisation of ICP-OES for single elements using simplex techniques identified an ICP torch fitted with a wide bore injector tube as most suitable for multielement analysis because of a compact analytical region in the plasma. A suitable objective function has been proposed for multielement simplex optimisation of ICP-OES and its effectiveness has been demonstrated. The effects of easily ionisable element (EIE) interferences have been studied and an interference minimisation simplex optimisation shown to be appropriate for the location of an interference free zone. Routine, interference free determinations (<2% for 0.5% Na) have been shown to be critically dependant on the stability of the injector gas flowrate and nebuliser derived pressure pulses. Discrete nebulisation has been investigated for the analysis of small fragments of a variety of metal alloys which could be encountered in casework investigations. External contamination together with alloy inhomogeneity have been shown to present some problems in the interpretation of the data. A compact, corrosion resistant recirculating nebuliser has been constructed and evaluated for the analysis of small fragments of shotgun steels. The stable aerosol production from this nebuliser allowed a set of element lines, free from iron interferences, to be monitored with a scanning monochromator. The analysis, classification and discrimination of casework sized fragments of brasses and sheet glasses have been performed and a method has been proposed for the analysis of white household gloss paints. The determination of metal traces on hands following the handling of a variety of metal alloys has been reported. The significance of the results from these evidential materials has been assessed for forensic science purposes.
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Clarke, Philip Alexander. "Solid sample introduction in Inductively Coupled Plasma Emission Spectrometry." Thesis, Sheffield Hallam University, 1988. http://shura.shu.ac.uk/19472/.

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This Thesis describes the progress made in the area of solid sample introduction in Inductively Coupled Plasma Emission Spectrometry (ICP-ES). As an alternative to solution nebulisation two methods of introducing samples to the ICP are investigated. The first of these uses the direct insertion probe technique first described by Horlick and Salin (63). The assembly utilised an electrically operated graphite rod system. This could be used equally well with small volumes of solution sample (5ul) or small masses of solid sample (Ca.5mg). The variables of cup dimensions and material were investigated along with volume and masses of sample used. Results of calibration of both solution residues and solid samples are presented along with details of Limit of Detection and sample Relative Standard Deviation (RSD). The comparative data were found to be in good agreement and it was established that solutions derived calibration data could be used for the analysis of Ni-base samples. Other solid matrices, elemental and alloyed were investigated. These materials divided into two groups, (1) low volatility matrix, from which trace elements were released and only minimal emission from matrix elements was detected and there were no spectral interference effects, (2) volatile matrix in which the matrix vaporized in the same temperature range as the trace elements, giving rise to substantial matrix emission and spectral interferences. It was concluded that DI-ICP-ES is at its most useful when dealing with easily volatilized trace elements in a relatively involatile matrix. The second approach to sample introduction involved the use of an electrothermal vaporization cell. This provided precise control of temperature and offered considerably higher final temperatures than the direct insertion probe system. An Electrothermal Vaporization (ETV) device was designed and built in the laboratory and interfaced to the ICP such that vapour produced in the cell was carried into the plasma discharge by the 'injector' gas stream. ETV was used for liquid and solid samples and results for these samples are presented.
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Wang, Liang. "Analysis of Galvanized Steel Plates Using Glow Discharge-Atomic Emission Spectrometry." TopSCHOLAR®, 1999. http://digitalcommons.wku.edu/theses/762.

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Combining an intense emission source and a high-speed sputtering source in one, glow discharge atomic emission spectrometer (GD-AES) provides an efficient technique for analyzing surfaces, coatings and bulk solids. The purpose of our work is to explore the optimum lamp operation parameters of SA-2000 for analysis of galvanized steel plate and to investigate the method for qualitatively and quantitatively analyzing the zinc coating. Under the optimum experimental conditions found in our study, which are current of 19-21 mA; voltage of 900-1200 V; pressure 2.0-2.5 torr, the calibration curve is constructed, so that specific zinc concentration can be assign to the exact depth position in the sample. Several galvanized steel plate samples are tested and the thickness of coating and distribution of zinc in different depth of the coating are calculated on the basis of calibration curve. The above results are further analyzed to prove the reproducibility of the proposed method.
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Ruiz, Annia I. "Sample introduction for low pressure microwave induced plasma atomic emission spectrometry." Thesis, Georgia Institute of Technology, 1992. http://hdl.handle.net/1853/30324.

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Books on the topic "Flame atomic emission spectrometry"

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Kagakkai, Nihon Bunseki, ed. ICP hakkō bunseki: ICP atomic emission spectrometry. Tōkyō-to Bunkyo-ku: Kyōritsu Shuppan, 2013.

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Thompson, Michael. Handbook of inductively coupled plasma atomic emission spectrometry. Woking: Viridian Publishing, 2003.

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Introduction to inductively coupled plasma atomic emission spectrometry. Amsterdam: Elsevier, 1989.

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Analytical atomic spectrometry with flames and plasmas. Weinheim: Wiley-VCH, 2001.

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Boss, Charles B. Concepts, instrumentation, and techniques in inductively coupled plasma atomic spectrometry. [s.l.]: Perkin Elmer, 1989.

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Moore, G. L. Internal standardization in atomic-emission spectrometry using inductively coupled plasma. Randburg, South Africa: Council for Mineral Technology, 1985.

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CRC handbook of inductively coupled plasma atomic emission spectroscopy. Boca Raton: CRC Press, 1991.

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Boss, Charles B. Concepts, instrumentation and techniques in inductively coupled plasma atomic emission spectrometry. [USA]: Perkin Elmer, 1989.

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Ziara, K. S. Stability and atomic line studies of a Dc arc for low resolution atomic emission spectrometry. Manchester: UMIST, 1994.

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Inductively coupled plasma atomic emission spectrometry: A model multi-elemental technique for modern analytical laboratory. Hauppauge, N.Y: Nova Science Publishers, 2011.

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Book chapters on the topic "Flame atomic emission spectrometry"

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Baker, Dale E., and Norman H. Suhr. "Atomic Absorption and Flame Emission Spectrometry." In Agronomy Monographs, 13–27. Madison, WI, USA: American Society of Agronomy, Soil Science Society of America, 2015. http://dx.doi.org/10.2134/agronmonogr9.2.2ed.c2.

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Wright, Robert J., and Tomasz Stuczynski. "Atomic Absorption and Flame Emission Spectrometry." In SSSA Book Series, 65–90. Madison, WI, USA: Soil Science Society of America, American Society of Agronomy, 2018. http://dx.doi.org/10.2136/sssabookser5.3.c4.

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Zimmermann, S., S. Wischhusen, and J. Müller. "A μTAS — Atomic Emission Flame Spectrometer (AES)." In Micro Total Analysis Systems 2000, 135–38. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-017-2264-3_31.

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Broekaert, J. A. C. "Atomic Emission Spectrometry." In Glow Discharge Spectroscopies, 113–74. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4899-2394-3_4.

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Rosenberg, Erwin, and Ulrich Panne. "Atomic Absorption Spectrometry (AAS) and Atomic Emission Spectrometry (AES)." In Handbook of Spectroscopy, 421–96. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527602305.ch12.

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Rosenberg, Erwin, and Ulrich Panne. "Atomic Absorption Spectrometry (AAS) and Atomic Emission Spectrometry (AES)." In Handbook of Spectroscopy, 507–82. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527654703.ch15.

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Potts, P. J. "Inductively coupled plasma—atomic emission spectrometry." In A Handbook of Silicate Rock Analysis, 153–97. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4615-3270-5_5.

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Potts, P. J. "Inductively coupled plasma-atomic emission spectrometry." In A Handbook of Silicate Rock Analysis, 153–97. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-015-3988-3_5.

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Miller, Dennis D., and Michael A. Rutzke. "Atomic Absorption Spectroscopy, Atomic Emission Spectroscopy, and Inductively Coupled Plasma-Mass Spectrometry." In Food Science Texts Series, 421–42. Boston, MA: Springer US, 2010. http://dx.doi.org/10.1007/978-1-4419-1478-1_24.

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Yeung, Vincent, Dennis D. Miller, and Michael A. Rutzke. "Atomic Absorption Spectroscopy, Atomic Emission Spectroscopy, and Inductively Coupled Plasma-Mass Spectrometry." In Food Science Text Series, 129–50. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-45776-5_9.

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Conference papers on the topic "Flame atomic emission spectrometry"

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McCurry, Cynthia K., and Robert R. Romanosky. "Sampling and Analysis of Alkali in High-Temperature, High-Pressure Gasification Streams." In ASME 1985 International Gas Turbine Conference and Exhibit. American Society of Mechanical Engineers, 1985. http://dx.doi.org/10.1115/85-gt-202.

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This paper describes the experiences leading to successful sampling of hot, contaminated, coal-derived gas streams for alkali constituents using advanced spectrometers. This activity was integrated with a multi-phase, combustion test program which addressed the use of minimally treated, coal-derived fuel gas in gas turbines. Alkali contaminants in coal-derived fuels are a source of concern, as they may induce corrosion of and deposition on turbine components. Real-time measurement of alkali concentrations in gasifier output fuel gas streams is important in evaluating these effects on turbine performance. An automated, dual-channel, flame atomic emission spectrometer was used to obtain on-line measurements of total sodium and potassium mass loadings (vapors and particles) in two process streams at the General Electric fixed-bed coal gasifier and turbine combustor simulator facility in Schenectady, New York. Alkali measurements were taken on (1) slipstreams of high temperature, high pressure, minimally clean, low-Btu fuel gas containing entrained particles from the gasifier and (2) a slipstream of the exhaust gas from the combustor/turbine simulator. Alkali detection limits for the analyzer were found to be on the order of one part per billion. Providing a representative sample to the alkali analyzer at the limited flows required by the instrument was a major challenge of this activity. Several approaches and sampling hardware configurations were utilized with varying degrees of success during this testing campaign. The resulting information formed the basis for a second generation sampling system which has recently been successfully utilized to measure alkali concentrations in slipstreams from the described fixed-bed coal gasifier and turbine combustor simulator.
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Salkauskas, Julius. "Trends of investigations on atomic analytical emission spectrometry (AES) in Lithuania." In IV Workshop on Atomic and Molecular Physics, edited by Jozef Heldt. SPIE, 2003. http://dx.doi.org/10.1117/12.544390.

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Xue, Jun, Shengfang Gong, Yulan Fan, and Xun Li. "Indirect Determination of Mercury in Traditional Chinese Medicine by Flame Atomic Absorption Spectrometry." In 2011 5th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2011. http://dx.doi.org/10.1109/icbbe.2011.5781512.

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Liu, Q. "Research of Trace Elements Content in Tea Based on Flame Atomic Absorption Spectrometry." In International Conference on Materials Chemistry and Environmental Protection 2015. Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/meep-15.2016.13.

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Oralova, A. T., K. K. Malikov, and E. A. Ceshkovskaya. "Investigation of the gold content in activated carbon by atomic emission spectrometry." In General question of world science. L-Journal, 2020. http://dx.doi.org/10.18411/gq-30-11-2020-16.

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In this article, we developed and tested a method for acid preparation of activated carbon samples for analysis using hydrofluoric acid, followed by analysis of samples for gold content using the iCAP 7400 Duo atomic emission spectrometer. The analysis of the experimental results showed the possibility of using the atomic emission method with inductively coupled plasma as a reliable and expressive method for determining the concentration of gold in activated carbon, which will optimize the operation of a gold mining enterprise.
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Sakamoto, Soji, Juichi Saito, Toshihiko Kishimoto, and Kozo Ishida. "Particulate Characterization of Automotive Emissions by Helium Microwave-Induced Plasma Atomic Emission Spectrometry." In International Congress & Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1997. http://dx.doi.org/10.4271/971017.

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Liu, Quan-De, Shang-Long Chen, Yong Li, Jing Gao, and Yun-Xu Zhu. "Determination of Iron and Zinc in Garbanzo by Microwave Digestion-High Resolution Continuum Source Flame Atomic Absorption Spectrometry." In 5th International Conference on Advanced Design and Manufacturing Engineering. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/icadme-15.2015.188.

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Hao, Xiaojian, Zhenhua Liu, and Tao Sang. "Temperature measurement of wood flame based on the double line method of atomic emission spectra." In Selected Proceedings of the Chinese Society for Optical Engineering Conferences held November 2015, edited by Weimin Bao and Yueguang Lv. SPIE, 2016. http://dx.doi.org/10.1117/12.2228222.

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Cheng, Yong. "Determination of Matrix Element Sodium in the Sodium Metavanadate by Inductively Coupled Plasma Atomic Emission Spectrometry?" In International Conference on Chemical,Material and Food Engineering. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/cmfe-15.2015.212.

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Xiang-Lian, Peng, Li Zhong-Hai, and Qiang Dun-Zhi. "Determination of cadmium content in the food paper and plastic packaging materials with wet digestion-flame atomic absorption spectrometry." In 2012 International Conference on Biobase Material Science and Engineering (BMSE). IEEE, 2012. http://dx.doi.org/10.1109/bmse.2012.6466180.

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Reports on the topic "Flame atomic emission spectrometry"

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Urbansky, Edward T. Sustainability of Rotrode Atomic Emission Spectrometry for Wear Deris. Fort Belvoir, VA: Defense Technical Information Center, October 2006. http://dx.doi.org/10.21236/ada473827.

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2

Montaser, A. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/7203155.

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3

Montaser, A. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6303748.

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4

Montaser, A. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/6252073.

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5

Urasa, I. T. The use of ion chromatography-dc plasma atomic emission spectrometry for the speciation of trace metals. Office of Scientific and Technical Information (OSTI), September 1991. http://dx.doi.org/10.2172/5637324.

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6

Gallimore, David L. 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). Office of Scientific and Technical Information (OSTI), June 2012. http://dx.doi.org/10.2172/1043523.

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7

Montaser, A. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Progress report, January 1, 1990--December 31, 1992. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/10182145.

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Montaser, A. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Progress report, January 1, 1994--December 31, 1994. Office of Scientific and Technical Information (OSTI), September 1994. http://dx.doi.org/10.2172/10181234.

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9

Montaser, A. New high temperature plasmas and sample introduction systems for analytical atomic emission and mass spectrometry. Progress report: January 1, 1993--December 31, 1993. Office of Scientific and Technical Information (OSTI), December 1993. http://dx.doi.org/10.2172/10110330.

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10

Urasa, I. T. The use of ion chromatography-dc plasma atomic emission spectrometry for the speciation of trace metals. Annual performance report, February 1, 1989--January 31, 1992. Office of Scientific and Technical Information (OSTI), September 1991. http://dx.doi.org/10.2172/10133010.

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