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Sample records for plasma-atomic emission spectroscopy

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2002-09-01

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

  2. Zinc, lead and copper in human teeth measured by induced coupled argon plasma atomic emission spectroscopy (ICP-AES)

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    Chew, L.T.; Bradley, D.A. E-mail: D.A.Bradley@exeter.ac.uk; Mohd, Y.; Jamil, M

    2000-11-15

    Inductively Coupled Argon Plasma Atomic Emission Spectroscopy (ICP-AES) has been used to determine Pb, Zn and Cu levels in 47 exfoliated human teeth (all of which required extraction for orthodontic reasons). Lead concentrations for the group were 1.7 {mu}g (g tooth mass){sup -1} to 40.5 {mu}g (g tooth mass){sup -1}, with a median of 9.8 {mu}g (g tooth mass){sup -1}. A median lead level in excess of the group value was found for the teeth of six lorry drivers who were included in the study. A more significant enhancement was found for the seven subjects whose age was in excess of 60 years. The median values for Zn and Cu were 123.0 and 0.6 {mu}g (g tooth mass){sup -1} respectively. Present values for tooth-Zn are lower than published data for other ethnic groups.

  3. Fingerprinting of complex mixtures with the use of high performance liquid chromatography, inductively coupled plasma atomic emission spectroscopy and chemometrics

    Energy Technology Data Exchange (ETDEWEB)

    Ni Yongnian [Department of Chemistry, Nanchang University, Nanchang, Jiangxi 330047 (China)], E-mail: ynni@ncu.edu.cn; Peng Yunyan [Department of Chemistry, Nanchang University, Nanchang, Jiangxi 330047 (China); Kokot, Serge [Inorganic Materials Program, School of Physical and Chemical Sciences, Queensland University of Technology, Brisbane, Queensland 4001 (Australia)

    2008-05-26

    The molecular and metal profile fingerprints were obtained from a complex substance, Atractylis chinensis DC-a traditional Chinese medicine (TCM), with the use of the high performance liquid chromatography (HPLC) and inductively coupled plasma atomic emission spectroscopy (ICP-AES) techniques. This substance was used in this work as an example of a complex biological material, which has found application as a TCM. Such TCM samples are traditionally processed by the Bran, Cut, Fried and Swill methods, and were collected from five provinces in China. The data matrices obtained from the two types of analysis produced two principal component biplots, which showed that the HPLC fingerprint data were discriminated on the basis of the methods for processing the raw TCM, while the metal analysis grouped according to the geographical origin. When the two data matrices were combined into a one two-way matrix, the resulting biplot showed a clear separation on the basis of the HPLC fingerprints. Importantly, within each different grouping the objects separated according to their geographical origin, and they ranked approximately in the same order in each group. This result suggested that by using such an approach, it is possible to derive improved characterisation of the complex TCM materials on the basis of the two kinds of analytical data. In addition, two supervised pattern recognition methods, K-nearest neighbors (KNNs) method, and linear discriminant analysis (LDA), were successfully applied to the individual data matrices-thus, supporting the PCA approach.

  4. Elemental Content in Brown Rice by Inductively Coupled Plasma Atomic Emission Spectroscopy Reveals the Evolution of Asian Cultivated Rice

    Institute of Scientific and Technical Information of China (English)

    Yawen Zeng; Luxiang Wang; Juan Du; Jiafu Liu; Shuming Yang; Xiaoying Pu; Fenghui Xiao

    2009-01-01

    The phylogenetic relationship for classification traits and eight mineral elements in brown rice (Oryza sativa L.) from Yunnan Province in China was carried out using microwave assisted digestion followed by inductively coupled plasma atomic emission spectroscopy, and the analytical procedures were carefully controlled and validated. In general, the results show that the mean levels of K, Ca, Mg, Fe and Cu in brown rice for 789 accessions of rice landraces was distinctly lower than that of improved cultivars. They further demonstrate that Ca plays an important role in the differentiation of subspecies indica-japonica, especially to enhance adaptation of cold stress, and that five mineral elements in brown rice enhance the eurytopicity from landrace to improved cultivar. Hierarchical cluster analysis, using average linkage from SPSS software based on eight mineral elements in brown rice, showed that Yunnan rice could be grouped into rice landrace and improved cultivar, with the rice landrace being further clustered into five subgroups, and that, interestingly, purple rice does not cluster with either of the groups. Our present data confirm that indica is the closest relative of late rice and white rice, and that they constitute rice landraces together, whereas japonica is the closest relatives of non-nuda, early-mid and glutinous rice. It is further shown that japonica, non-nuda, early-mid, glutinous, white and red rice might be more primitive than indica, nuda, late, non-glutinous and purple rice, respectively.

  5. Standard test method for determining elements in waste Streams by inductively coupled plasma-atomic emission spectroscopy

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 This test method covers the determination of trace, minor, and major elements in waste streams by inductively coupled plasma-atomic emission spectroscopy (ICP-AES) following an acid digestion of the sample. Waste streams from manufacturing processes of nuclear and non-nuclear materials can be analyzed. This test method is applicable to the determination of total metals. Results from this test method can be used to characterize waste received by treatment facilities and to formulate appropriate treatment recipes. The results are also usable in process control within waste treatment facilities. 1.2 This test method is applicable only to waste streams that contain radioactivity levels that do not require special personnel or environmental protection. 1.3 A list of the elements determined in waste streams and the corresponding lower reporting limit is found in Table 1. 1.4 This test method has been used successfully for treatment of a large variety of waste solutions and industrial process liquids. The com...

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

    Energy Technology Data Exchange (ETDEWEB)

    SEIDEL CM; JAIN J; OWENS JW

    2009-02-23

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

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

    Directory of Open Access Journals (Sweden)

    K. Rehan

    2017-01-01

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

  8. Investigation of biodistribution behavior of platinum particles in mice: Correlation between inductively coupled plasma-atomic emission spectroscopy and X-ray scanning analytical microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Abe, Shigeaki, E-mail: sabe@den.hokudai.ac.jp [Graduate School of Dental Medicine, Hokkaido University, Sapporo (Japan); Koyama, Chika; Mutoh, Mami [Faculty of Dental Medicine, Hokkaido University, Sapporo (Japan); Akasaka, Tsukasa [Graduate School of Dental Medicine, Hokkaido University, Sapporo (Japan); Uo, Motohiro [Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo (Japan); Watari, Fumio [Graduate School of Dental Medicine, Hokkaido University, Sapporo (Japan)

    2012-12-01

    Highlights: Black-Right-Pointing-Pointer We investigated the biodistribution of platinum microparticles in mice. Black-Right-Pointing-Pointer The biodistribution behavior was observed using inductively coupled plasma-atomic emission spectroscopy (ICP) and scanning X-ray analytical microscopy (XSAM). Black-Right-Pointing-Pointer The administered particles quickly reached in spleen, liver and lung with constant ration. Black-Right-Pointing-Pointer We also estimated the correlation ship between XSAM and ICP measurement. Black-Right-Pointing-Pointer The relative ratio of XSAM intensity showed highly correlation with the relative ratio of Pt concentration in organs. - Abstract: In this study, we investigated the biodistribution of platinum (Pt) microparticles in mice. The particles were administered through the tail vein, and then the biodistribution behavior was observed using inductively coupled plasma-atomic emission spectroscopy (ICP) and scanning X-ray analytical microscopy (XSAM). The administered particles quickly reached the spleen, liver, and lung at a constant ratio, and the ratio remained constant for four weeks. We also estimated the correlation between XSAM and ICP measurement. The relative ratio of XSAM intensity showed strong correlation with the relative ratio of Pt concentration in organs.

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

    Science.gov (United States)

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

    2011-07-01

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

  10. Application of inductively coupled plasma atomic emission spectroscopy analysis with a polychromator/monochromator combination the byproducts of coal-fired power stations

    Science.gov (United States)

    Weers, C. A.

    The by-products of coal-fired power plants may be hazardous for the environment. Good analysis methods are therefore required in order to establish either a possible usage of the by-products or their possible storage. Preliminary experiments performed with inductively coupled plasma atomic emission spectroscopy have proven very successful. Moreover, the method is cost-effective. A short description is given of the optimized system for routine analysis. The system consists of a 2- and a 15-channel polychromator in combination with a monochromator. The opportunities is provides are also described. Use of the monochromator to analyze coal and run-off water from the flue-gases desulphurization, and of the polychromators to analyze coal fly-ash is described separately.

  11. Determination of some inorganic metals in edible vegetable oils by inductively coupled plasma atomic emission spectroscopy (ICP-AES

    Directory of Open Access Journals (Sweden)

    Musa Özcan, M.

    2008-09-01

    Full Text Available Seventeen edible vegetable oils were analyzed spectrometrically for their metal (Cu, Fe, Mn, Co, Cr, Pb, Cd, Ni, and Zn contents. Toxic metals in edible vegetable oils were determined by Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES. The highest metal concentrations were measured as 0.0850, 0.0352, 0.0220, 0.0040, 0.0010, 0.0074, 0.0045, 0.0254 and 0.2870 mg/kg for copper in almond oil, for iron in corn oil-(c, for manganese in soybean oil, for cobalt in sunflower oil-(b and almond oil, for chromium in almond oil, for lead in virgin olive oil, for cadmium in sunflower oil-(e, for nickel almond oil and for zinc in almond oil respectively. The method for determining toxic metals in edible vegetable oils by using ICP-AES is discussed. The metals were extracted from low quantities of oil (2-3 g with a 10% nitric acid solution. The extracted metal in acid solution can be injected into the ICPAES. The proposed method is simple and allows the metals to be determined in edible vegetable oils with a precision estimated below 10% relative standard deviation (RSD for Cu, 5% for Fe, 15% for Mn, 8% for Co, 10% for Cr, 20% for Pb, 5% for Cd, 16% for Ni and 11% for Zn.En este estudio se analizó espectrométricamente el contenido en metales (Cu, Fe, Mn, Co, Cr, Pb, Cd, Ni, and Zn de 17 aceites vegetales comestibles mediante ICP-AES. Las concentaciones más elevadas se encontraron para el cobre en el aceite de almendra (0.0850 mg/kg, para el hierro en el aceite de maiz(c,(0.0352 mg/kg, para el manganeso en el aceite de soja (0.0220 mg/kg, para el cobalto en el aceite de girasol (b (0.0040 mg/kg, para el cromo en el aceite de almendra (0.0010 mg/kg, para el plomo en el aceite de oliva virgen (0.0074 mg/kg, para el cadmio en el aceite de girasol (e (0.0045 mg/kg, para el niquel en el aceite de almendra (0.0254 mg/kg y para el zincen el aceite de almendra (0.2870 mg/kg. Los metales se extrajeron a partir de bajas cantidades de aceite (2-3 g, con

  12. Development of novel and sensitive methods for the determination of sulfide in aqueous samples by hydrogen sulfide generation-inductively coupled plasma-atomic emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Colon, M. [Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona (Spain); Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain); Todoli, J.L. [Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain); Hidalgo, M. [Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona (Spain); Iglesias, M. [Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona (Spain)], E-mail: monica.iglesias@udg.es

    2008-02-25

    Two new, simple and accurate methods for the determination of sulfide (S{sup 2-}) at low levels ({mu}g L{sup -1}) in aqueous samples were developed. The generation of hydrogen sulfide (H{sub 2}S) took place in a coil where sulfide reacted with hydrochloric acid. The resulting H{sub 2}S was then introduced as a vapor into an inductively coupled plasma-atomic emission spectrometer (ICP-AES) and sulfur emission intensity was measured at 180.669 nm. In comparison to when aqueous sulfide was introduced, the introduction of sulfur as H{sub 2}S enhanced the sulfur signal emission. By setting a gas separator at the end of the reaction coil, reduced sulfur species in the form of H{sub 2}S were removed from the water matrix, thus, interferences could be avoided. Alternatively, the gas separator was replaced by a nebulizer/spray chamber combination to introduce the sample matrix and reagents into the plasma. This methodology allowed the determination of both sulfide and sulfate in aqueous samples. For both methods the linear response was found to range from 5 {mu}g L{sup -1} to 25 mg L{sup -1} of sulfide. Detection limits of 5 {mu}g L{sup -1} and 6 {mu}g L{sup -1} were obtained with and without the gas separator, respectively. These new methods were evaluated by comparison to the standard potentiometric method and were successfully applied to the analysis of reduced sulfur species in environmental waters.

  13. Building and analyzing models from data by stirred tank experiments for investigation of matrix effects caused by inorganic matrices and selection of internal standards in Inductively Coupled Plasma-Atomic Emission Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Grotti, Marco [Dipartimento di Chimica e Chimica Industriale, Via Dodecaneso 31, 16146 Genova (Italy)], E-mail: grotti@chimica.unige.it; Paredes, Eduardo; Maestre, Salvador; Todoli, Jose Luis [Departamento de Quimica Analitica, Nutricion y Bromatologia, Universidad de Alicante, 03080, Alicante (Spain)

    2008-05-15

    Interfering effects caused by inorganic matrices (inorganic acids as well as easily ionized elements) in inductively coupled plasma-atomic emission spectroscopy have been modeled by regression analysis of experimental data obtained using the 'stirred tank method'. The main components of the experimental set-up were a magnetically-stirred container and two peristaltic pumps. In this way the matrix composition was gradually and automatically varied, while the analyte concentration remained unchanged throughout the experiment. An inductively coupled plasma spectrometer with multichannel detection based on coupled charge device was used to simultaneously measure the emission signal at several wavelengths when the matrix concentration was modified. Up to 50 different concentrations were evaluated in a period of time of 10 min. Both single interfering species (nitric, hydrochloric and sulphuric acids, sodium and calcium) and different mixtures (aqua regia, sulfonitric mixture, sodium-calcium mixture and sodium-nitric acid mixture) were investigated. The dependence of the emission signal on acid concentration was well-fitted by logarithmic models. Conversely, for the easily ionized elements, 3-order polynomial models were more suitable to describe the trends. Then, the coefficients of these models were used as 'signatures' of the matrix-related signal variations and analyzed by principal component analysis. Similarities and differences among the emission lines were highlighted and discussed, providing a new insight into the interference phenomena, mainly with regards to the combined effect of concomitants. The combination of the huge amount of data obtained by the stirred tank method in a short period of time and the speed of analysis of principal component analysis provided a judicious means for the selection of the optimal internal standard in inductively coupled plasma-atomic emission spectroscopy.

  14. Simultaneous Cu-, Fe-, and Zn-specific detection of metalloproteins contained in rabbit plasma by size-exclusion chromatography-inductively coupled plasma atomic emission spectroscopy.

    Science.gov (United States)

    Manley, Shawn A; Byrns, Simon; Lyon, Andrew W; Brown, Peter; Gailer, Jürgen

    2009-01-01

    Analytical methods which are capable of determining the plasma or serum metalloproteome have inherent diagnostic value for human diseases associated with increased or decreased concentrations of specific plasma metalloproteins. We have therefore systematically developed a method to rapidly determine the major Cu-, Fe-, and Zn-containing metalloproteins in rabbit plasma (0.5 mL) based on size-exclusion chromatography (SEC; stationary phase Superdex 200, mobile phase phosphate-buffered saline pH 7.4) and the simultaneous online detection of Cu, Fe, and Zn in the column effluent by an inductively coupled plasma atomic emission spectrometer (ICP-AES). Whereas most previous studies reported on the analysis of serum, our investigations clearly demonstrated that the analysis of plasma within 30 min of collection results in the detection of one more Cu peak (blood coagulation factor V) than has been previously reported (transcuprein, ceruloplasmin, albumin-bound Cu, and small molecular weight Cu). The average amount of Cu associated with these five proteins corresponded to 21, 18, 21, 30 and 10% of total plasma Cu, respectively. In contrast, only two Fe metalloproteins (ferritin and transferrin, corresponding to an average of 9 and 91% of total plasma Fe) and approximately five Zn metalloproteins (alpha(2)-macroglobulin and albumin-bound Zn, which corresponded to an average of 10 and 57% of total [corrected] plasma Zn) were detected. Metalloproteins were assigned on the basis of the coelution of the corresponding metal and protein identified by immunoassays or activity-based enzyme assays. The SEC-ICP-AES approach developed allowed the determination of approximately 12 Cu, Fe, and Zn metalloproteins in rabbit plasma within approximately 24 min and can be applied to analyze human plasma, which is potentially useful for diagnosing Cu-, Fe-, and Zn-related diseases.

  15. Improvement of AOAC Official Method 984.27 for the determination of nine nutritional elements in food products by Inductively coupled plasma-atomic emission spectroscopy after microwave digestion: single-laboratory validation and ring trial.

    Science.gov (United States)

    Poitevin, Eric; Nicolas, Marine; Graveleau, Laetitia; Richoz, Janique; Andrey, Daniel; Monard, Florence

    2009-01-01

    A single-laboratory validation (SLV) and a ring trial (RT) were undertaken to determine nine nutritional elements in food products by inductively coupled plasma-atomic emission spectroscopy in order to improve and update AOAC Official Method 984.27. The improvements involved optimized microwave digestion, selected analytical lines, internal standardization, and ion buffering. Simultaneous determination of nine elements (calcium, copper, iron, potassium, magnesium, manganese, sodium, phosphorus, and zinc) was made in food products. Sample digestion was performed through wet digestion of food samples by microwave technology with either closed or open vessel systems. Validation was performed to characterize the method for selectivity, sensitivity, linearity, accuracy, precision, recovery, ruggedness, and uncertainty. The robustness and efficiency of this method was proved through a successful internal RT using experienced food industry laboratories. Performance characteristics are reported for 13 certified and in-house reference materials, populating the AOAC triangle food sectors, which fulfilled AOAC criteria and recommendations for accuracy (trueness, recovery, and z-scores) and precision (repeatability and reproducibility RSD and HorRat values) regarding SLV and RT. This multielemental method is cost-efficient, time-saving, accurate, and fit-for-purpose according to ISO 17025 Norm and AOAC acceptability criteria, and is proposed as an improved version of AOAC Official Method 984.27 for fortified food products, including infant formula.

  16. Combination of the ionic-to-atomic line intensity ratios from two test elements for the diagnostic of plasma temperature and electron number density in Inductively Coupled Plasma Atomic Emission Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Tognoni, E. [Istituto per i Processi Chimico-Fisici, Area della Ricerca del Consiglio Nazionale delle Ricerche Via Moruzzi 1, 56124 Pisa (Italy)], E-mail: tognoni@ipcf.cnr.it; Hidalgo, M.; Canals, A. [Departamento de Quimica Analitica, Nutricion y Bromatologia. Universidad de Alicante. Apdo. 99, 03080, Alicante (Spain); Cristoforetti, G.; Legnaioli, S.; Salvetti, A.; Palleschi, V. [Istituto per i Processi Chimico-Fisici, Area della Ricerca del Consiglio Nazionale delle Ricerche Via Moruzzi 1, 56124 Pisa (Italy)

    2007-05-15

    In Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) spectrochemical analysis, the MgII(280.270 nm)/MgI(285.213 nm) ionic to atomic line intensity ratio is commonly used as a monitor of the robustness of operating conditions. This approach is based on the univocal relationship existing between intensity ratio and plasma temperature, for a pure argon atmospheric ICP in thermodynamic equilibrium. In a multi-elemental plasma in the lower temperature range, the measurement of the intensity ratio may not be sufficient to characterize temperature and electron density. In such a range, the correct relationship between intensity ratio and plasma temperature can be calculated only when the complete plasma composition is known. We propose the combination of the line intensity ratios of two test elements (double ratio) as an effective diagnostic tool for a multi-elemental low temperature LTE plasma of unknown composition. In particular, the variation of the double ratio allows us discriminating changes in the plasma temperature from changes in the electron density. Thus, the effects on plasma excitation and ionization possibly caused by introduction of different samples and matrices in non-robust conditions can be more accurately interpreted. The method is illustrated by the measurement of plasma temperature and electron density in a specific analytic case.

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

    Science.gov (United States)

    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%.

  18. Transition probabilities for lines of Cr II, Na II and Sb I by laser produced plasma atomic emission spectroscopy; Probabilidades de transicion de algunos niveles de Cr II, Na II y Sb I medediante espectroscopia de plasma producidos por laser

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez, A. M.; Ortiz, M.; Campos, J.

    1995-07-01

    Absolute transition probabilities for lines of CR II, Na II and Sb I were determined by emission spectroscopy of laser induced plasmas. the plasma was produced focusing the emission of a pulsed Nd-Yag laser on solid samples containing the atom in study. the light arising from the plasma region was collected by and spectrometer. the detector used was a time-resolved optical multichannel analyzer (OMA III EG and G). The wavelengths of the measured transitions range from 2000 sto 4100 A. The spectral resolution of the system was 0. 2 A. The method can be used in insulators materials as Cl Na crystals and in metallic samples as Al-Cr and Sn-Sn alloys. to avoid self-absorption effects the alloys were made with low Sb or Cr content. Relative transition probabilities have been determined from measurements of emission-line intensities and were placed on an absolute scale by using, where possible, accurate experimental lifetime values form the literature or theoretical data. From these measurements, values for plasma temperature (8000-24000 K), electron densities ({approx}{approx} 10''16 cm ''-3) and self-absorption coefficients have been obtained. (Author) 56 refs.

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

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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.

  3. Determination of myo-inositol hexakisphosphate (phytate) in urine by inductively coupled plasma atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Grases, F.; Perello, J.; Isern, B.; Prieto, R.M

    2004-05-10

    Myo-inositol hexakisphosphate (phytate) is a substance present in urine with an important role in preventing calcium renal calculi development. In spite of this, the use of urinary phytate levels on stone-formers' evaluation and treatment is still notably restricted as a consequence of the enormous difficulty to analyze this substance in urine. In this paper, a simple procedure for routinary urinary phytate determination based on phosphorus determination through inductively coupled plasma atomic emission spectrometry is described. The method only requires a previous separation of phytate from other components by column anion exchange chromatography. The working linear range used was 0-2 mg l{sup -1} phosphorus (0-7 mg l{sup -1} phytate). The limit of detection was 64 {mu}g l{sup -1} of phytate and the limit of quantification was 213 {mu}g l{sup -1}. The relative standard deviation (R.S.D.) for 1.35 mg l{sup -1} phytate was 2.4%. Different urine samples were analyzed using an alternative analytical methodology based on gas chromatography (GC)/mass detection used for inositol determination (phytate was previously hydrolyzed), resulting both methods comparable using as criterion to assess statistical significance P<0.05.

  4. Determination of trace elements in refined gold samples by inductively coupled plasma atomic emission spectrometry

    Directory of Open Access Journals (Sweden)

    Steharnik Mirjana

    2013-01-01

    Full Text Available This paper presents a method for determination the trace contents of silver, copper, iron, palladium, zinc and platinum in refined gold samples. Simultaneous inductively coupled plasma atomic emission spectrometer with radial torch position and cross flow nebulizer was used for determination. In order to compare the different calibration strategies, two sets of calibration standards were prepared. The first set was based on matrix matched calibration standards and the second was prepared without the addition of matrix material. Detection limits for matrix matching calibrations were higher for some elements than those without matrix matching. In addition, the internal standardization method was applied and experiments indicated that indium was the best option as internal standard. The obtained results for gold sample by matrix matching and matrix free calibrations were compared with the obtained results by standard addition method. The accuracy of the methods was tested performing recovery test. Recoveries for spiked sample were in the range of 90-115 %. The accuracy of the methods was also tested by analysis of certified reference material of high pure goldAuGHP1. The best results were achieved by matrix free calibration and standard addition method using indium as internal standard at wavelength of 230 nm. [Projekat Ministarstva nauke Republike Srbije, br. 34024: Development of Technologies for Recycling of Precious, Rare and Associated Metals from Solid Waste in Serbia to High Purity Products

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

    Science.gov (United States)

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

    2010-08-03

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

  6. Inductively coupled plasma--atomic emission spectrometry: trace elements in oil matrices

    Energy Technology Data Exchange (ETDEWEB)

    Peterson, C. A.

    1977-12-01

    The simultaneous determination of up to 20 trace elements in various oil matrices by inductively coupled plasma-atomic emission spectrometry is reported. The oil matrices investigated were lubricating oils (for wear metals), fuel oil, centrifuged coal liquefaction product, crude soybean oil, and commercial edible oils. The samples were diluted with appropriate organic solvents and injected into the plasma as an aerosol generated by a pneumatic nebulization technique. Detection limits of the 28 elements studied ranged from 0.0006 to 9 ..mu..g/g with the majority falling in the 0.01 to 0.1 ..mu..g/g range. Analytical calibration curves were linear over at least two orders of magnitude and for some elements this linearity extended over 4.5 orders of magnitude. Relevant data on precision and accuracy are included. Because metals often occur as particles in lubricating oil and coal liquefaction products, the effect of particles on the analytical results was examined. Wear metal particles in used oil did not appear to affect the analytical results. However, incomplete recovery relative to organometallic reference solutions was obtained for iron particles with a nominal mean diameter of 3.0 ..mu..m suspended in oil. It was shown that the following factors contributed to incomplete recovery for the particles: settling of the suspended particles in the flask, a difference in nebulization efficiency between particle suspensions and organometallic solutions, and indications of incomplete vaporization of the larger particles in the plasma.

  7. Standard practice for analysis of aqueous leachates from nuclear waste materials using inductively coupled plasma-atomic emission spectrometry

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 This practice is applicable to the determination of low concentration and trace elements in aqueous leachate solutions produced by the leaching of nuclear waste materials, using inductively coupled plasma-atomic emission spectroscopy (ICP-AES). 1.2 The nuclear waste material may be a simulated (non-radioactive) solid waste form or an actual solid radioactive waste material. 1.3 The leachate may be deionized water or any natural or simulated leachate solution containing less than 1 % total dissolved solids. 1.4 This practice should be used by analysts experienced in the use of ICP-AES, the interpretation of spectral and non-spectral interferences, and procedures for their correction. 1.5 No detailed operating instructions are provided because of differences among various makes and models of suitable ICP-AES instruments. Instead, the analyst shall follow the instructions provided by the manufacturer of the particular instrument. This test method does not address comparative accuracy of different devices...

  8. Elemental analysis using instrumental neutron activation analysis and inductively coupled plasma atomic emission spectrometry: a comparative study

    Energy Technology Data Exchange (ETDEWEB)

    Chung, Yong Sam; Choi, Kwang Soon; Moon, Jong Hwa; Kim, Sun Ha; Lim, Jong Myoung; Kim, Young Jin [KAERI, Taejon (Korea, Republic of); Quraishi, Shamshad Begum [Bangladesh Atomic Energy Commission, Dhaka (Bangladesh)

    2003-05-01

    Elemental analyses for certified reference materials were carried out using instrumental neutron activation analysis and inductively coupled plasma-atomic emission spectrometry. Five Certified Reference Materials (CRM) were selected for the study on comparative analysis of environmental samples. The CRM are Soil (NIST SRM 2709), Coal fly ash (NIST SRM 1633a), urban dust (NIST SRM 1649a) and air particulate on filter media (NIST SRM 2783 and human hair (GBW 09101)

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

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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.

  12. Evaluation of arsenic and selenium in Brazilian soluble coffee by inductively coupled plasma atomic emission spectrometry with hydride generation

    Directory of Open Access Journals (Sweden)

    Santos Éder José dos

    2001-01-01

    Full Text Available A method for the evaluation of arsenic and selenium in soluble coffee by inductively coupled plasma atomic emission spectrometry with continuous hydride generation to attend the Brazilian food legislation is described. Samples were digested with nitric acid and hydrogen peroxide in a focused microwave system. Slow heating eliminated nitric acid and selenium (VI was reduced to selenium (IV by addition of 6 mol/L hydrochloric acid and heating at 90° C under a reflux system. The influence of sample acidity on sensitivity was investigated. Hydrochloric acid 6 mol/L was the most suitable reaction medium. Practical detection limits of 2.0mug/L for As and 1.0mu g/L for Se were achieved and attended the Brazilian food legislation. The results of recoveries on spiked samples demonstrate the reliability and accuracy of the procedure.

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

    Science.gov (United States)

    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.

  14. Determination of micro yttrium in an ytterbium matrix by inductively coupled plasma atomic emission spectrometry and wavelet transform

    Institute of Scientific and Technical Information of China (English)

    MA Xiaoguo

    2005-01-01

    In the determination of trace yttrium (Y) in an ytterbium (Yb) matrix by inductively coupled plasma atomic emission spectrometry (ICP-AES), the most prominent line of yttrium, Y 371.030 nm line, suffers from strong interference due to an emission line of ytterbium. In this work, a method based on wavelet transform was proposed for the spectral interference correction. Haar wavelet was selected as the mother wavelet. The discrete detail after the third decomposition, D3,was chosen for quantitative analysis based on the consideration of both separation degree and peak height. The linear correlation coefficient between the height of the left positive peak in D3 and the concentration of Y was calculated to be 0.9926.Six synthetic samples were analyzed, and the recovery for yttrium varied from 96.3% to 110.0%. The amounts of yttrium in three ytterbium metal samples were determined by the proposed approach with an average relative standard deviation (RSD)of 2.5%, and the detection limit for yttrium was 0.016%. This novel correction technique is fast and convenient, since neither complicated model assumption nor time-consuming iteration is required. Furthermore, it is not affected by the wavelength drift inherent in monochromators that will severely reduce the accuracy of results obtained by some chemometric methods.

  15. Determination of Uranium in Apatite Minerals by Solvent Extraction--Inductively Coupled Plasma Atomic Emission Spectrometry

    OpenAIRE

    1993-01-01

    [Abstract] Solvent, extraction-ICP atomic emission spectrometry was applied to the determination of uranium in apatite minerals. Apatite minerals were treated with nitric acid. After removing a small quantity of insoluble residue, uranium was extracted with 0.05 mol/dm^3 1-phonyl-3-mcthyl-4-trifluoroacetyl-5-pyrazolonc-diisobutyl kctone at pH 0.8. The uranium content in the apatite was found to be (20.3〜132.9)×10^%.

  16. Evaluation of vapor generation for the determination of nickel by inductively coupled plasma-atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Marrero, Julieta [Comision Nacional de Energia Atomica, Unidad de Actividad Quimica, Centro Atomico Constituyentes, Av. Gral. Paz 1499, 1650-San Martin, Pcia. de Buenos Aires (Argentina); Smichowski, Patricia [Comision Nacional de Energia Atomica, Unidad Proyectos Especiales de Suministros Nucleares, Av. Libertador 8250, 1429-Buenos Aires (Argentina)

    2002-09-01

    Volatile species of Ni were generated by merging acidified aqueous samples and sodium tetrahydroborate(III) in a continuous flow system. The gaseous analyte was subsequently introduced via a stream of Ar carrier into the inlet tube of the plasma torch. Inductively coupled plasma atomic emission spectrometry (ICP-AES) was used for detection. The operating conditions (chemical and physical parameters) and the concentrations of different acids were evaluated for the efficient generation of Ni vapor. The detection limit (3 {sigma}{sub blank}) was 1.8 ng mL{sup -1}. The precision (RSD) of the determination was 4.2% at a level of 500 ng mL{sup -1} and 7.3% for 20 ng mL{sup -1} (n=10). The efficiency of the generation process was estimated to be 51%. The possible interfering effect of transition metals (Cd, Co, Cu, Cr, Fe, Mn, Zn), hydride forming elements (As, Ge, Pb, Sb, Se, Sn, Te), and Hg on Ni signal was examined. This study has demonstrated that Ni vapor generation is markedly free of interferences. (orig.)

  17. Analysis of tree leaves, bark and wood by sequential inductively coupled argon plasma atomic emission spectrometry

    Science.gov (United States)

    Verbeek, A. A.

    The analysis of extracts from tree leaf, bark and wood samples for Ca, Mg, K, Na, P, Mn, Fe, Al, B, Cu and Zn by inductively coupled argon plasma sequential emission spectrometry is described. Recovery percentages for simulated tree extracts and for spiked tree samples are presented together with typical analysis values for a leaf and a wood sample. The choice of analytical line for each element is discussed and spectral interferences, not listed in the ICP tables of Boumans, of Cu on the 214.9 nm line of P and of Fe on the 249.7 nm line of B are noted.

  18. Determination of {sup 233}U by inductively coupled argon plasma - atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Patwardhan, A.B.; Kulkarni, V.T.; Radhakrishnan, K.; Ramanujam, A.; Page, A.G. [Bhabha Atomic Research Centre, Bombay (India)

    1994-09-01

    The paper describes studies carried out for the determination of {sup 233}U at various stages during the recovery and purification of {sup 233}U from {sup 233}U-Al alloy scraps generated during the fabrication of {sup 233}U-Al alloy fuel. Employing a high resolution sequential spectrometer and Inductively Coupled argon Plasma (ICP) as the spectral excitation source, isotope shift for {sup 233}U with respect to {sup 238}U has been resolved and recorded. The shift for the 424.437 nm emission line of {sup 238}U is found to be of the order of 0.040 nm on the lower wavelength side for {sup 233}U and this isotopic effect has been utilised for the quantitative determination of {sup 233}U. The overall precision of the method is 5% RSD with the detection limit of 0.01 {mu}g/ml.

  19. Use of stirred tanks for studying matrix effects caused by inorganic acids, easily ionized elements and organic solvents in inductively coupled plasma atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Paredes, Eduardo [Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain); Maestre, Salvador E. [Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain); Todoli, Jose L. [Departamento de Quimica Analitica, Nutricion y Bromatologia, University of Alicante, 03080 Alicante (Spain)]. E-mail: jose.todoli@ua.es

    2006-03-15

    A stirred tank was used for the first time to elucidate the mechanism responsible for inductively coupled plasma atomic emission spectroscopy (ICP-AES) matrix effects caused by inorganic, acids and easily ionized elements (EIEs), as well as organic, ethanol and acetic acid, compounds. In order to gradually increase the matrix concentration, a matrix solution was introduced inside a stirred container (tank) initially filled with an aqueous multielement standard. PolyTetraFluoroEthylene (PTFE) tubing was used to deliver the resulting solution to the liquid sample introduction system. Matrix concentration ranged from 0 to 2 mol l{sup -1} in the case of inorganic acids (i.e., nitric, sulfuric, hydrochloric and a mixture of them), from 0 to about 2500 mg l{sup -1} for EIEs (i.e., sodium, calcium and mixtures of both) and from 0% to 15%, w/w for organic compounds. Up to 40-50 different solutions were prepared and measured in a period of time shorter than 6-7 min. This investigation was carried out in terms of emission intensity and tertiary aerosols characteristics. The experimental setup used in the present work allowed to thoroughly study the effect of matrix concentration on analytical signal. Generally speaking, the experiments concerning tertiary aerosol characterization revealed that, in the case of inorganic acids and EIEs, the mechanism responsible for changes in aerosol characteristics was the droplet fission. In contrast, for organic matrices it was found that the interference was caused by a change in both aerosol transport and plasma thermal characteristics. The extent of the interferences caused by organic as well as inorganic compounds was compared for a set of 14 emission lines through a wide range of matrix concentrations. With a stirred tank, it is possible to choose an efficient internal standard for any given matrix composition. The time required to complete this procedure was shorter than 7 min.

  20. Volatile organo-selenium speciation in biological matter by solid phase microextraction–moderate temperature multicapillary gas chromatography with microwave induced plasma atomic emission spectrometry detection

    OpenAIRE

    Dietz, Christian; Sanz Landaluze, Jon; Ximenez Embun, Pilar; Madrid Albarrán, Yolanda; Cámara, Carmen

    2004-01-01

    Microwave induced plasma atomic emission spectrometry (MIP-AES) in combination with multicapillary (MC) gas chromatography could be proven to be useful for element specific detection of volatile species. Solid phase microextraction (SPME) was used for preconcentration and sample-matrix separation. The fiber desorption unit as well as the heating control for the MCcolumn were in-house developed and multicapillary column was operated at moderate temperatures (30–100 ◦C). The method was...

  1. The use of ion chromatography-dc plasma atomic emission spectrometry for the speciation of trace metals

    Energy Technology Data Exchange (ETDEWEB)

    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.

  2. Separation of gold, palladium and platinum in chromite by anion exchange chromatography for inductively coupled plasma atomic emission spectrometric analysis

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Kwang Soon; Lee, Chang Heon; Park, Yeong Jae; Joe, Kih Soo; Kim, Won Ho [KAERI, Taejon (Korea, Republic of)

    2001-08-01

    A study has been carried out on the separation of gold, iridium, palladium, rhodium, ruthenium and platinum in chromite samples and their quantitative determination using inductively coupled plasma atomic emission spectrometry (ICP-AES). The dissolution condition of the minerals by fusion with sodium peroxide was optimized and chromatographic elution behavior of the rare metals was investigated by anion exchange chromatography. Spectral interference of chromium, a matrix of the minerals, was investigated on determination of gold. Chromium interfered on determination of gold at the concentration of 500 mg/L and higher. Gold plus trace amounts of iridium, palladium, rhodium and ruthenium, which must be preconcentrated before ICP-AES was separated by anion exchange chromatography after reducing Cr(VI) to Cr(III) by H{sub 2}O{sub 2}. AuCl{sup -}{sub 4} retained on the resin column was selectively eluted with acetone- HNO{sub 3}-H{sub 2}O as an eluent. In addition, iridium, palladium, rhodium and ruthenium remaining on the resin column were eluted as a group with concentrated HCl. However, platinum was eluted with concentrated HNO{sub 3}. The recovery yield of gold with acetone-HNO{sub 3}-H{sub 2}O was 100.7 {+-} 2.0 % , and the yields of palladium and platinum with concentrated HCl and HNO{sub 3} were 96.1 {+-} 1.8% and 96.6 {+-} 1.3%, respectively. The contents of gold and platinum in a Mongolian chromite sample were 32.6 {+-} 2.2 {mu}g/g and 1.6 {+-} 0.14 {mu}g/g, respectively. Palladium was not detected.

  3. Determination of nickel in biological materials after microwave dissolution using inductively coupled plasma atomic emission spectrometry with prior extraction into butan-1-ol.

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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

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

    Science.gov (United States)

    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.

  6. 电感耦合等离子体-原子发射光谱法的应用%Application of Inductively Coupled Plasma-Atomic Emission Spectrometry

    Institute of Scientific and Technical Information of China (English)

    时亮; 隋欣

    2013-01-01

    The application of inductively coupled plasma-atomic emission spectrometry in animal and plant analysis, environmental analysis, metallurgical analysis, electric power production, food analysis, lithium niobate analysis, harmful heavy metals detection in toys, and the cultural relics protection, etc, were summarized.%  综述了利用电感耦合高频等离子体作为激发光源的原子发射光谱法在动植物分析、环境分析、冶金分析、电力生产、食品分析、铌酸锂分析、玩具中有害重金属测定及文物保护科学研究等方面中的应用。

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

    Science.gov (United States)

    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.

  8. Determination of Phosphorus by Inductively Coupled Plasma Atomic Emission Spectroscopy after Hydride Generation

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A continuous phosphine (PH3) generation was developed and applied to the sensitive detection of phosphorus by ICP-AES. Phosphate ion in aqueous solution was converted to phosphine by passing the sample solution through an incandescent copper silica-tube. Detection limit is 2 ng/mL. The relative standard deviation is 4.2% for 20 ng/mL. The method is rapid and simple with low contamination and high sensitivity.

  9. Simultaneous determination of some trace metal impurities in high-purity sodium tungstate using coprecipitation and inductively coupled plasma atomic emission spectrometry

    Institute of Scientific and Technical Information of China (English)

    MA Xiaoguo; KUANG Tongchun; LIU Qianjun

    2004-01-01

    A method based on the combination of coprecipitation with inductively coupled plasma atomic emission spec trometry (ICP-AES) was developed for the determination of impurities in high-purity sodium tungstate. Six elements (Co,Cu, Fe, Mn, Ni, and Pb) were coprecipitated by lanthanum hydroxide so as to be concentrated and separated from the tungsten matrix. Effects of some factors on the recoveries of the analytes and on the residual amount of sodium tungstate were investigated, and the optimum conditions for the coprecipitation were proposed. Matrix-matching calibration curve method was used for the analysis. It is shown that the elements mentioned above can be quantitatively recovered. The detection limits for Co, Cu, Fe, Mn, Ni, and Pb are 0.07, 0.4, 0.2, 0.1, 0.6, and 1.3 μg.g-1, respectively. The recoveries vary from 92.5% to 108%, and the relative standard deviations (RSDs) are in the range of 3.1%-5.5%.

  10. Volatile organo-selenium speciation in biological matter by solid phase microextraction-moderate temperature multicapillary gas chromatography with microwave induced plasma atomic emission spectrometry detection

    Energy Technology Data Exchange (ETDEWEB)

    Dietz, C.; Sanz Landaluze, J.; Ximenez-Embun, P.; Madrid-Albarran, Y.; Camara, C

    2004-01-16

    Microwave induced plasma atomic emission spectrometry (MIP-AES) in combination with multicapillary (MC) gas chromatography could be proven to be useful for element specific detection of volatile species. Solid phase microextraction (SPME) was used for preconcentration and sample-matrix separation. The fiber desorption unit as well as the heating control for the MC column were in-house developed and multicapillary column was operated at moderate temperatures (30-100 deg. C). The method was optimized for organo-selenium species (dimethylselenide (DMSe), diethylselenide (DEtSe) and dimethyldiselenide (DMDSe)), using a chemometric approach. Stationary phases for the separation column were optimized using a conventional GC and contrasted with the results obtained with the MC. Application was focussed on selenium accumulating biological matter, such as lupine, yeast, Indian mustard and garlic. These samples were grown in hydroponic solution containing inorganic selenium (Na{sub 2}SeO{sub 3} and Na{sub 2}SeO{sub 4}). SPME sampling was carried out in fixed volume flow boxes in headspace above the living plants and in vials using treated samples. Results demonstrate inorganic selenium transformation into volatile organic species during metabolism. Separation is fast, a chromatogram can be obtained in less than 3 min and detection limits were at sub-ppb level for all investigated species. The system is independent from the use of a conventional gas chromatographic oven and can be used as a versatile alternative to highly cost intensive methods such as GC-ICP-MS.

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

    Science.gov (United States)

    Ozbek, Nil; Akman, Suleyman

    2016-06-01

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

  12. Slurry sampling fluorination assisted electrothermal vaporization-inductively coupled plasma-atomic emission spectrometry for the direct determination of metal impurities in aluminium oxide ceramic powders.

    Science.gov (United States)

    Peng, T; Chang, G; Wang, L; Jiang, Z; Hu, B

    2001-03-01

    A new analytical procedure for the direct determination of metal impurities (Cr, Cu, Fe and V) in aluminium oxide ceramic powders by slurry sampling fluorination assisted electrothermal vaporization-inductively coupled plasma-atomic emission spectrometry (ETV-ICP-AES) is reported. A polytetrafluoroethylene (PTFE) emulsion was used as a fluorinating reagent to promote the vaporization of impurity elements in aluminium oxide ceramic powders from the graphite tube. A vaporization stage with a long ramp time and a short hold time provided the possibility of temporal analyte-matrix separation. The experimental results indicated that a 10 microL 1% m/v slurry of aluminium oxide could be destroyed and vaporized completely with 600 micrograms PTFE under the selected conditions. Two aluminium oxide ceramic powder samples were used without any additional pretreatment. Analytical results obtained by using standard addition method with aqueous standard solution were checked by comparison of the results with pneumatic nebulization (PN)-ICP-AES based on the wet-chemical decomposition and analyte-matrix separation. The limits of detection (LODs) between 0.30 microgram g-1 (Fe) and 0.08 microgram g-1 (Cu) were achieved, and, the repeatability of measurements was mainly better than 10%.

  13. Microwave-assisted versus conventional decomposition procedures applied to a ceramic potsherd standard reference material by inductively coupled plasma atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

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

    2004-03-03

    Inductively coupled plasma atomic emission spectrometry (ICP-AES) is a powerful, sensitive analytical technique with numerous applications in chemical characterization including that of ancient pottery, mainly due to its multi-element character, and the relatively short time required for the analysis. A critical step in characterization studies of ancient pottery is the selection of a suitable decomposition procedure for the ceramic matrix. The current work presents the results of a comparative study of six decomposition procedures applied on a standard ceramic potsherd reference material, SARM 69. The investigated decomposition procedures included three microwave-assisted decomposition procedures, one wet decomposition (WD) procedure by conventional heating, one combined microwave-assisted and conventional heating WD procedure, and one fusion procedure. Chemical analysis was carried out by ICP-AES. Five major (Si, Al, Fe, Ca, Mg), three minor (Mn, Ba, Ti) and two trace (Cu, Co) elements were determined and compared with their certified values. Quantitation was performed at two different spectral lines for each element and multi-element matrix-matched calibration standards were used. The recovery values for the six decomposition procedures ranged between 75 and 110% with a few notable exceptions. Data were processed statistically in order to evaluate the investigated decomposition procedures in terms of recovery, accuracy and precision, and eventually select the most appropriate one for ancient pottery analysis.

  14. 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

    Science.gov (United States)

    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.

  15. 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

    Energy Technology Data Exchange (ETDEWEB)

    Petrova, P.; Velichkov, S. [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, Acad. G. Bontchev Str. bl. 11, 1113 Sofia (Bulgaria); Velitchkova, N. [Geological Institute, Bulgarian Academy of Sciences, Acad. G. Bontchev Str., bl.24, 1113 Sofia (Bulgaria); Havezov, I. [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, Acad. G. Bontchev Str. bl. 11, 1113 Sofia (Bulgaria); Daskalova, N., E-mail: das15482@svr.igic.bas.b [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, Acad. G. Bontchev Str. bl. 11, 1113 Sofia (Bulgaria)

    2010-02-15

    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{sup -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.

  16. Multielement determination of heavy metals in water samples by continuous powder introduction microwave-induced plasma atomic emission spectrometry after preconcentration on activated carbon

    Science.gov (United States)

    Jankowski, Krzysztof; Yao, Jun; Kasiura, Krzysztof; Jackowska, Adrianna; Sieradzka, Anna

    2005-03-01

    A novel continuous powder introduction microwave-induced plasma atomic emission spectrometry method (CPI-MIP-AES) has been developed for trace determination of metals in ground and tap water samples after preconcentration on activated carbon. The experimental setup consisted of integrated rectangular cavity TE 101 and vertically positioned plasma torch. The technical arrangement of the sample introduction system has been designed based on the fluidized bed concept. The satisfactory signal stability required for sequential analysis was attained owing to the vertical plasma configuration, as well as the plasma gas flow rate compatibility with sample introduction flow rate. The elements of interest (Cd, Cu, Cr, Fe, Mn, Pb, Zn) were preconcentrated in a batch procedure at pH 8-8.5 after addition of activated carbon and then, after filtering and drying of the activated carbon suspension, introduced to the MIP by the CPI system. An enrichment factor of about 1000-fold for a sample volume of 1 l was obtained. The detection limit values for the proposed method were 17-250 ng l -1. The proposed method was validated by analyzing the certified reference materials: SRW "Warta" Synthetic River Water and BCR CRM 399 major elements in freshwater. The method was successfully applied to the determination of the heavy metals in tap water samples.

  17. Multielement determination of heavy metals in water samples by continuous powder introduction microwave-induced plasma atomic emission spectrometry after preconcentration on activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Jankowski, Krzysztof [Warsaw University of Technology, Faculty of Chemistry, Department of Analytical Chemistry, 00-664 Warsaw, ul. Noakowskiego 3 (Poland)]. E-mail: kj@ch.pw.edu.pl; Yao Jun [College of Chemistry and Chemical Engineering, Jishou University, 120 Renmin South Road, Jishou 416000 (China); Kasiura, Krzysztof [Warsaw University of Technology, Faculty of Chemistry, Department of Analytical Chemistry, 00-664 Warsaw, ul. Noakowskiego 3 (Poland); Jackowska, Adrianna [Warsaw University of Technology, Faculty of Chemistry, Department of Analytical Chemistry, 00-664 Warsaw, ul. Noakowskiego 3 (Poland); Sieradzka, Anna [Warsaw University of Technology, Faculty of Chemistry, Department of Analytical Chemistry, 00-664 Warsaw, ul. Noakowskiego 3 (Poland)

    2005-03-31

    A novel continuous powder introduction microwave-induced plasma atomic emission spectrometry method (CPI-MIP-AES) has been developed for trace determination of metals in ground and tap water samples after preconcentration on activated carbon. The experimental setup consisted of integrated rectangular cavity TE{sub 101} and vertically positioned plasma torch. The technical arrangement of the sample introduction system has been designed based on the fluidized bed concept. The satisfactory signal stability required for sequential analysis was attained owing to the vertical plasma configuration, as well as the plasma gas flow rate compatibility with sample introduction flow rate. The elements of interest (Cd, Cu, Cr, Fe, Mn, Pb, Zn) were preconcentrated in a batch procedure at pH 8-8.5 after addition of activated carbon and then, after filtering and drying of the activated carbon suspension, introduced to the MIP by the CPI system. An enrichment factor of about 1000-fold for a sample volume of 1 l was obtained. The detection limit values for the proposed method were 17-250 ng l{sup -1}. The proposed method was validated by analyzing the certified reference materials: SRW 'Warta' Synthetic River Water and BCR CRM 399 major elements in freshwater. The method was successfully applied to the determination of the heavy metals in tap water samples.

  18. Particle transport in a He-microchip plasma atomic emission system with an ultrasonic nebulizer for aqueous sample introduction

    Science.gov (United States)

    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.

  19. Investigations on the on-line determination of metals in air flows by capacitively coupled microwave plasma atomic emission spectrometry

    Science.gov (United States)

    Seelig, M.; Broekaert, J. A. C.

    2001-09-01

    Plasma optical emission spectrometry with a capacitively coupled microwave plasma (CMP) operated with air has been investigated with respect to its possibilities for real-time environmental monitoring of combustion processes. The unique feature is the possibility to operate the CMP with air as working gas, as is usually the case in exhaust gases of combustion processes. The CMP also is shown to be stable in the presence of large amounts of water and CO 2, which makes this source ideally suitable for this purpose. The detection limits obtained for the environmentally relevant elements Cd, Co, Cr, Fe, Mg, Ni and Pb show the possibility to monitor directly heavy metals in air in an on-line mode and down to the 2-160-μg m -3 level. These detection limits are generally lower than the threshold limit values of the 'Federal Law for Immission Protection' in Germany in the gaseous effluents of industrial plants. In order to investigate the influence of the water loading (32-222 g m -3) on the detection limits a comparison of results obtained with three different nebulizers (Légère nebulizer, hydraulic high-pressure nebulizer and ultrasonic nebulizer) was made, with which aerosols with different water loading are entered into the plasma. For the hydraulic high-pressure nebulizer and the ultrasonic nebulizer no desolvation unit was found to be necessary. It was shown that especially for elements with lines having high excitation energy (Cd) or for which ion lines are used (Mg II) the increase in water loading deteriorates the detection limits. The rotational temperatures ( Trot) and excitation temperatures ( Texe) in the case of different amounts of water are of the order of 3700-4900 K and 4700-7100 K, respectively. The temperatures show that changes in the geometry and temperature distribution in the case of Trot but also the values of Texe themselves are responsible for this increase in detection limits. Furthermore, different amounts of CO 2 mixed to the working gas (3

  20. Particle transport in a He-microchip plasma atomic emission system with an ultrasonic nebulizer for aqueous sample introduction

    Energy Technology Data Exchange (ETDEWEB)

    Oh, Joosuck [Department of Chemistry, Dankook University, 126 Jukjeon-dong, Suji-gu, Yongin-si, Gyeonggi-do, 448-701 (Korea, Republic of); Lim, H.B. [Department of Chemistry, Dankook University, 126 Jukjeon-dong, Suji-gu, Yongin-si, Gyeonggi-do, 448-701 (Korea, Republic of)], E-mail: plasma@dankook.ac.kr

    2008-11-15

    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 ({approx} 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{sup -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{sup -1} were nebulized, transported particles were obtained with a mass range of 0.5-5 mg m{sup -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 deg. C). The limits of detection obtained for K, Na and Cu were 0.26, 0.22, and 0.28 mg L{sup -1}, respectively. These results confirmed the suitable stability and sensitivity of the He-rf-PDMS microchip plasma for application as an atomization source.

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

    Science.gov (United States)

    Beiraghi, Assadollah; Babaee, Saeed

    2008-01-28

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

  2. 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

    Energy Technology Data Exchange (ETDEWEB)

    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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Beiraghi, Assadollah [Faculty of Chemistry, Tarbiat Moallem University, Mofatteh Avenue, No. 49, P.O. Box 15614, Tehran (Iran, Islamic Republic of)], E-mail: Beiraghi@Saba.tmu.ac.ir; Babaee, Saeed [Faculty of Chemistry, Tarbiat Moallem University, Mofatteh Avenue, No. 49, P.O. Box 15614, Tehran (Iran, Islamic Republic of)

    2008-01-28

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

  4. Ultrasound bath-assisted enzymatic hydrolysis procedures as sample pretreatment for the multielement determination in mussels by inductively coupled plasma atomic emission spectrometry.

    Science.gov (United States)

    Peña-Farfal, Carlos; Moreda-Piñeiro, Antonio; Bermejo-Barrera, Adela; Bermejo-Barrera, Pilar; Pinochet-Cancino, Hugo; de Gregori-Henríquez, Ida

    2004-07-01

    Ultrasound energy has been applied to speed up enzymatic hydrolysis processes of mussel tissue in order to determine trace and ultratrace elements (As, Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn). The element releases, by action of three proteases (pepsin, pancreatin, trypsin), lipase, and alpha-amylase, have been evaluated by inductively coupled plasma atomic emission spectrometry. Different variables such as pH, sonication temperature, ionic strength, hydrolysis time, ultrasound frequency, extracting volume, and enzyme mass were simultaneously studied by applying an experimental design approach (Plackett-Burman design and central composite design). Results showed that the hydrolysis time was statistically nonsignificant (confidence interval of 95%) for most of the elements and enzymes, meaning that the hydrolysis procedure can be finished within a 30-60-min range. These hydrolysis times are far shorter than those obtained when using thermostatic cameras, between 12 and 24 h. Statistically significant factors were the ultrasound frequency (the highest metals releasing at high-ultrasound frequency), pH, sonication temperature, and ionic strength. All metals can be extracted using the same operating conditions (pH of 1.0 and sodium chloride at 1.0% for pepsin; pH of 7.5, temperature at 37 degrees C, and 0.4 M potassium dihydrogen phosphate/potassium hydrogen phosphate buffer for amylase; pH of 8.0 and 0.5 M potassium dihydrogen phosphate/potassium hydrogen phosphate buffer for pancreatin; pH of 5.0 and 0.5 M potassium dihydrogen phosphate/potassium hydrogen phosphate buffer for lipase; pH of 8.0 and 0.2 M potassium dihydrogen phosphate/potassium hydrogen phosphate buffer for trypsin). Analytical performances, such as limits of detection and quantification, repeatability of the overall procedure, and accuracy, by analyzing DORM-1, DORM-2, and TORT-1 certified reference materials, were finally assessed for each enzyme.

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

    Energy Technology Data Exchange (ETDEWEB)

    Papadopoulou, D.N. [Laboratory of Analytical Chemistry, Faculty of Chemistry, Aristotle University, GR-54124, Thessaloniki (Greece); Zachariadis, G.A. [Laboratory of Analytical Chemistry, Faculty of Chemistry, Aristotle University, GR-54124, Thessaloniki (Greece); Anthemidis, A.N. [Laboratory of Analytical Chemistry, Faculty of Chemistry, Aristotle University, GR-54124, Thessaloniki (Greece); Tsirliganis, N.C. [Archaeometry Laboratory, Cultural and Educational Technology Institute, Tsimiski 58, GR-67100, Xanthi (Greece); Stratis, J.A. [Laboratory of Analytical Chemistry, Faculty of Chemistry, Aristotle University, GR-54124, Thessaloniki (Greece)]. E-mail: jstratis@chem.auth.gr

    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)

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

    Science.gov (United States)

    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

  7. On-line cloud point extraction combined with electrothermal vaporization inductively coupled plasma atomic emission spectrometry for the speciation of inorganic antimony in environmental and biological samples

    Energy Technology Data Exchange (ETDEWEB)

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

    2006-08-25

    A new method for the determination of inorganic Sb species by on-line cloud point extraction combined with electrothermal vaporization inductively coupled plasma atomic emission spectrometry (ETV-ICP-AES) is presented and evaluated. The method is based on the complexation of Sb(III) with pyrrolidine dithiocarbamate (PDC) which form an hydrophobic complex at pH 5.5 and subsequently enter surfactant-rich phase at pH 5.5, whereas Sb(V) remained in aqueous solutions. The preconcentration step is mediated by micelles of the non-ionic surfactant Triton X-114 with ammonium pyrrolidine dithiocarbamate (APDC). The micellar system containing the complex was loaded into the FIA manifold at a flow rate of 2.5 mL min{sup -1}, and the surfactant-rich phase was retained in a microcolumn packed with absorbent cotton, at pH 5.5. After the surfactant-rich phase was eluted with 100 {mu}L acetonitrile, it was determined by ETV-ICP-AES. Sb(V) is reduced to Sb(III) by L-cysteine prior to determined total Sb, and its assay is based on subtracting Sb(III) from total antimony. The main factors affecting separation/preconcentration and the vaporization behavior of analyte in graphite tube were investigated in detail. Under the optimized conditions, the precision relative standard deviation (R.S.D.) for eight replicate measurements of 0.2 {mu}g mL{sup -1} Sb(III) was 4.3%. The apparent concentration factor, which is defined as the concentration ratio of the analyte in the final diluted surfactant-rich extract ready for ETV-ICP-AES detection and in the initial solution, was 872 for Sb(III). The limit of detection (LOD) for Sb(III) was 0.09 {mu}g L{sup -1}. The proposed method was successfully applied for the speciation of inorganic antimony in different water samples and urine sample with satisfactory results.

  8. Determination of the mineral compositions of some selected oil-bearing seeds and kernels using Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES

    Directory of Open Access Journals (Sweden)

    Musa Özcan, M.

    2006-06-01

    Full Text Available The aim of this paper was to establish the mineral contents of oil-bearing seeds and kernels such as peanut, turpentine, walnut, hazelnut, sesame, corn, poppy, almond, sunflower etc., using Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES. Significant differences in mineral composition were observed among crops. All seeds and kernels contained high amounts of Al, Ca, Fe, K, Mg, Na, P and Zn. B, Cr, Cu, Li, Ni, Sr, Ti while V contents of the crops were found to be very low. The levels of K and P of all crops in this study were found to be higher than those of other seeds and kernels. The results obtained from analyses of the crops showed that the mean levels of potassiumcontent ranged from 1701.08 mg/kg (corn to 20895.8 mg/kg (soybean, the average content of phosphorus ranged from 3076.9 mg/kg (turpentine to 12006,5 mg/kg to 2617.4 mg/kg (cotton seed, and Ca from 68.4 mg/kg (corn to 13195.7 mg/kg (poppy seed. The results show that these values may  be useful for the evaluation of dietary information. Particularly the obtained results provide evidence that soybean, pinestone and poppy seed are a good source of K, P and Ca, respectively. Whereas pinestone is a good source of zinc.La finalidad del trabajo es establecer el contenido en elementos minerales de semillas oleaginosas tales como cacahuetes, trementina, avellana, sesamo, maiz, almendras, girasol, utilizando ICP-AES. Se han observado diferencias significativas en la composición de minerales entre cosechas. Todas las semillas contienen cantidades elevadas de Al, Ca, Fe, K, Mg, Na, P y Zn. Los contenidos de B, Cr, Cu, Li, Ni, Sr, Ti y V, sin embargo, fueron bajos. Los contenidos de K y P en todas las semillas estudiadas fueron superiores a las de otras semillas. El contenido medio de K osciló entre 1.701,1 mg/kg (maiz a 20.895,8 mg/kg (soja, el P entre 3.076.9 mg/kg (trementina a 12.006.5 mg/kg o 2.617,4 mg/kg (semilla de algodón, y Ca de 68,4 mg/kg (maiz a 13.195,7 mg

  9. Ultra-trace monitoring of copper in environmental and biological samples by inductively coupled plasma atomic emission spectrometry after separation and preconcentration by using octadecyl silica membrane disks modified by a new schiff's base

    Directory of Open Access Journals (Sweden)

    Mohammad Reza Ganjali

    2004-04-01

    Full Text Available Ultra-trace amounts of Cu(II were separated and preconcentrated by solid phase extraction on octadecyl-bonded silica membrane disks modified with a new Schiff,s base (Bis- (2-Hydroxyacetophenone -2,2-dimethyl-1,3-propanediimine (SBTD followed by elution and inductively coupled plasma atomic emission spectrometric detection. The method was applied as a separation and detection method for copper(II in environmental and biological samples. Extraction efficiency and the influence of sample matrix, flow rate, pH, and type and minimum amount of stripping acid were investigated. The concentration factor and detection limit of the proposed method are 500 and 12.5 pg mL-1, respectively.

  10. 电感耦合等离子体光谱法测定童鞋中的铬含量%Inductively Coupled Plasma-Atomic Emission Spectrometric (ICP-AES) Determination of Chromium in Children's Leather Shoes

    Institute of Scientific and Technical Information of China (English)

    刘贵深; 李婷; 侯晓东

    2012-01-01

    采用微波消解-电感耦合等离子体光谱法测定市场上不同厂家生产的童鞋中铬含量,对结果进行分析研究,找出重金属铬超标的原因并提出解决的对策,为降低健康安全风险,提高产品质量提供一定的参考依据。%Chromium content in children's leather shoes from different manufacturer was determined using microwave digestion and inductively coupled plasma-atomic emission spectrometry. This monitoring provides some references to reduce the health and safety risks, and improve the quality of products.

  11. Inductively coupled plasma-atomic emission spectroscopy: a computer controlled, scanning monochromator system for the rapid determination of the elements

    Energy Technology Data Exchange (ETDEWEB)

    Floyd, M.A.

    1980-03-01

    A computer controlled, scanning monochromator system specifically designed for the rapid, sequential determination of the elements is described. The monochromator is combined with an inductively coupled plasma excitation source so that elements at major, minor, trace, and ultratrace levels may be determined, in sequence, without changing experimental parameters other than the spectral line observed. A number of distinctive features not found in previously described versions are incorporated into the system here described. Performance characteristics of the entire system and several analytical applications are discussed.

  12. Assessing oral bioaccessibility of trace elements in soils under worst-case scenarios by automated in-line dynamic extraction as a front end to inductively coupled plasma atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Rosende, María [FI-TRACE group, Department of Chemistry, University of the Balearic Islands, Carretera de Valldemossa, km 7.5, Palma de Mallorca, Illes Balears E-07122 (Spain); Magalhães, Luis M.; Segundo, Marcela A. [REQUIMTE, Department of Chemistry, Faculty of Pharmacy, University of Porto, R. de Jorge Viterbo Ferreira, 228, Porto 4050-313 (Portugal); Miró, Manuel, E-mail: manuel.miro@uib.es [FI-TRACE group, Department of Chemistry, University of the Balearic Islands, Carretera de Valldemossa, km 7.5, Palma de Mallorca, Illes Balears E-07122 (Spain)

    2014-09-09

    Highlights: • Automatic oral bioaccessibility tests of trace metals under worst-case scenarios. • Use of intricate and realistic digestive fluids (UBM method). • Analysis of large amounts of soils (≥400 mg) in a flow-based configuration. • Smart interface to inductively coupled plasma atomic emission spectrometry. • Comparison of distinct flow systems mimicking physiological conditions. - Abstract: A novel biomimetic extraction procedure that allows for the in-line handing of ≥400 mg solid substrates is herein proposed for automatic ascertainment of trace element (TE) bioaccessibility in soils under worst-case conditions as per recommendations of ISO norms. A unified bioaccessibility/BARGE method (UBM)-like physiological-based extraction test is evaluated for the first time in a dynamic format for accurate assessment of in-vitro bioaccessibility of Cr, Cu, Ni, Pb and Zn in forest and residential-garden soils by on-line coupling of a hybrid flow set-up to inductively coupled plasma atomic emission spectrometry. Three biologically relevant operational extraction modes mimicking: (i) gastric juice extraction alone; (ii) saliva and gastric juice composite in unidirectional flow extraction format and (iii) saliva and gastric juice composite in a recirculation mode were thoroughly investigated. The extraction profiles of the three configurations using digestive fluids were proven to fit a first order reaction kinetic model for estimating the maximum TE bioaccessibility, that is, the actual worst-case scenario in human risk assessment protocols. A full factorial design, in which the sample amount (400–800 mg), the extractant flow rate (0.5–1.5 mL min{sup −1}) and the extraction temperature (27–37 °C) were selected as variables for the multivariate optimization studies in order to obtain the maximum TE extractability. Two soils of varied physicochemical properties were analysed and no significant differences were found at the 0.05 significance level

  13. 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.

    Science.gov (United States)

    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. Copyright © 2016 Elsevier B.V. All rights reserved.

  14. 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.

    Science.gov (United States)

    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.

  15. ICP-AES法测定土壤中的钾、锌、钒和钴%Determination of Potassium,Zinc,Vanadium,and Cobalt in Soil by Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES)

    Institute of Scientific and Technical Information of China (English)

    张继华; 张加萍

    2014-01-01

    Hydrochloric acid,nitric acid,hydrofluoric acid,and perchloric acid were applied to digest heavy met-als in soil sample.Inductively coupled plasma-atomic emission spectrometry (ICP-AES)method was employed to determine the contents of potassium,zinc,vanadium,and cobalt.The precision of this method to these four heavy metals was 3.09%for potassium,4.14%for zinc,3.76%for vanadium,and 3.85%for cobalt respective-ly.Generally,this method is simple and quick with wide linear range and few distractions.%采用盐酸-硝酸-氢氟酸-高氯酸全分解的方法消解,在选定的条件下以ICP-AES测定溶液中的K、Zn 、V 和Co含量,对国家标准物进行测定,方法精密度(RSD,n=16)为K 3.09%、Zn 4.14%、V 3.76%、Co3.85%。该方法具有线性范围宽、干扰少、快速、简便等优点,用于实样分析,结果令人满意。

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

    Directory of Open Access Journals (Sweden)

    Yajing Lou

    2014-01-01

    Full Text Available 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.

  17. 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

    Science.gov (United States)

    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

  18. Determination of borax in yuba by inductively coupled plasma atomic emission spectrometry with microwave digestion%微波消解-等离子体发射光谱法测定腐竹中硼砂

    Institute of Scientific and Technical Information of China (English)

    黄子伟; 王世平; 汤大鹏

    2012-01-01

    The dielectric assisted microwave digestion conditions were selected by orthogonal design, the experimental design was used to investigate the effect of four parameters: microwave power, mixed acid ratio, mixed acid volume and digestion time. And the borax in Yuba was determination with Inductively Coupled Plasma Atomic Emission Spectrometry after microwave digestion. The detection limit of the method was 0.4 mg/kg, the recoveries were in the rang of 91.2%~103.9%, and relative standard deviations were less than 2%.%采用正交试验设计优化介质辅助微波消解样品的条件,以电感耦合等离子体发射光谱法(ICP-AES)测定腐竹中硼砂。考察了微波消解功率、混合酸的比例、混合酸用量、试样消解时间4个因素在不同水平条件下对仪器响应值的影响。在优化了微波消解条件下测定实际样品,方法检出限为0.4mg/kg,加标回收率为91.2%~103.9%,相对标准偏差〈2%。

  19. 电感耦合等离子体原子发射光谱法测定银合金中的铂钯%Determination of Platinum and Palladium in Silver Alloy by Inductively Coupled Plasma Atomic Emission Spectrometry

    Institute of Scientific and Technical Information of China (English)

    佡云; 褚晓君

    2016-01-01

    采用硝酸溶解样品,盐酸沉淀分离银,过滤洗涤后,在5%(体积分数)硝酸介质中,用电感耦合等离子体原子发射光谱法(ICP-AES)测定银合金样品中的铂、钯,该方法用于多个银合金中铂钯的测定,加标回收率在96%~101%,相对标准偏差(RSD,n=10)小于5%。%The sample was dissolved with nitric acidhydrochloric acid was added to the sample to produce precipitation of silver chloridethen filter and wash it.Platinum and palladium in silver alloy samples are determinated by inductively coupled plasma atomic emission spectrometryICP-AES in a 5% volume fraction nitric acid .The method was applied to the determination of platinum and palladium in silver al-lay samples.The recovery rate was in the range of 96%~101% and the relative standard deviationRSDn=10 was less than 5%.

  20. 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.

    Science.gov (United States)

    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.

  1. Separation and preconcentration of Cd(II), Cu(II), Ni(II), and Pb(II) in water and food samples using Amberlite XAD-2 functionalized with 3-(2-nitrophenyl)-1H-1,2,4-triazole-5(4H)-thione and determination by inductively coupled plasma-atomic emission spectrometry.

    Science.gov (United States)

    Kumar, Bommana Naresh; Ramana, D K Venkata; Harinath, Yapati; Seshaiah, Kalluru; Wang, M C

    2011-10-26

    A separation and preconcentration procedure was developed for the determination of trace amounts of Cd(II), Cu(II), Ni(II), and Pb(II) in water and food samples using Amberlite XAD-2 fuctionalized with a new chelating ligand, 3-(2-nitrophenyl)-1H-1,2,4-triazole-5(4H)-thione (Amberlite XAD-2-NPTT). The chelating resin was characterized by Fourier transform infrared spectroscopy (FT-IR) and used as a solid sorbent for enrichment of analytes from samples. The sorbed elements were subsequently eluted with 10 mL of 1.0 M HNO(3), and the eluates were analyzed by inductively coupled plasma-atomic emission spectrometry. The influences of the analytical parameters including pH, amount of adsorbent, eluent type and volume, flow rate of the sample solution, volume of the sample solution, and effect of matrix on the preconcentration of metal ions have been studied. The optimum pH for the sorption of four metal ions was about 6.0. The limits of detection were found to be 0.22, 0.18, 0.20, and 0.16 μg L(-1) for Cd(II), Cu(II), Ni(II), and Pb(II), respectively, with a preconcentration factor 60. The proposed method was applied successfully for the determination of metal ions in water and food samples.

  2. Speciation analysis of organomercurial compounds in Fish Tissue by capillary gas chromatography coupled to microwave-induced plasma atomic emission detection

    Directory of Open Access Journals (Sweden)

    Dorfe Díaz

    Full Text Available This paper describes a novel approach for analysis of mercury speciation in fish using gas chromatography coupled with microwave-induced plasma optical emission spectrometry (GC-MIP-OES in surfatron resonant cavity. Sample treatment was based on quantitative leaching of mercury species from fish tissue with ultrasound-assisted acid-toluene extraction. The extracted mercury species analyzed with GC-MIP-OES attained detection limits of 5 and 9 pg for methylmercury (MeHg and ethylmercury (EtHg, respectively. A complete chromatogram could be completed in 1.5 min. MeHg values obtained with GC-MIP-OES were matched with organic mercury values obtained with selective reduction cold vapour- atomic absorption spectrometry (CV-AAS.

  3. 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

    Energy Technology Data Exchange (ETDEWEB)

    Hola, Marketa [Research Centre for Environmental Chemistry and Ecotoxicology and Laboratory of Atomic Spectrochemistry, Faculty of Science, Masaryk University in Brno, Kotlarska 2, CZ 611 37 Brno (Czech Republic); Otruba, Vitezslav [Research Centre for Environmental Chemistry and Ecotoxicology and Laboratory of Atomic Spectrochemistry, Faculty of Science, Masaryk University in Brno, Kotlarska 2, CZ 611 37 Brno (Czech Republic); Kanicky, Viktor [Research Centre for Environmental Chemistry and Ecotoxicology and Laboratory of Atomic Spectrochemistry, Faculty of Science, Masaryk University in Brno, Kotlarska 2, CZ 611 37 Brno (Czech Republic)]. E-mail: viktork@chemi.muni.cz

    2006-05-15

    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{sup 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

  4. 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

    Science.gov (United States)

    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

  5. Sequential-injection on-line preconcentration using chitosan resin functionalized with 2-amino-5-hydroxy benzoic acid for the determination of trace elements in environmental water samples by inductively coupled plasma-atomic emission spectrometry.

    Science.gov (United States)

    Sabarudin, Akhmad; Lenghor, Narong; Oshima, Mitsuko; Hakim, Lukman; Takayanagi, Toshio; Gao, Yun-Hua; Motomizu, Shoji

    2007-07-31

    A new chelating resin using chitosan as a base material was synthesized. Functional moiety of 2-amino-5-hydroxy benzoic acid (AHBA) was chemically bonded to the amino group of cross-linked chitosan (CCTS) through the arm of chloromethyloxirane (CCTS-AHBA resin). Several elements, such as Ag, Be, Cd, Co, Cu, Ni, Pb, U, V, and rare earth elements (REEs), could be adsorbed on the resin. To use the resin for on-line pretreatment, the resin was packed in a mini-column and installed into a sequential-injection/automated pretreatment system (Auto-Pret System) coupled with inductively coupled plasma-atomic emission spectrometry (ICP-AES). The sequential-injection/automated pretreatment system was a laboratory-assembled, and the program was written using Visual Basic software. This system can provide easy operation procedures, less reagent consumption, as well as less waste production. Experimental variables considered as effective factors in the improvement sensitivity, such as an eluent concentration, a sample and an eluent flow rate, pH of samples, and air-sandwiched eluent were carefully optimized. The proposed system provides excellent on-line collection efficiency, as well as high concentration factors of analytes in water samples, which results in highly sensitive detection of ultra-trace and trace analysis. Under the optimal conditions, the detection limits of 24 elements examined are in the range from ppt to sub-ppb levels. The proposed method was validated by using the standard reference material of a river water, SLRS-4, and the applicability was further demonstrated to the on-line collection/concentration of trace elements, such as Ag, Be, Cd, Co, Cu, Ni, Pb, U, V, and REEs in water samples.

  6. Assessing oral bioaccessibility of trace elements in soils under worst-case scenarios by automated in-line dynamic extraction as a front end to inductively coupled plasma atomic emission spectrometry.

    Science.gov (United States)

    Rosende, María; Magalhães, Luis M; Segundo, Marcela A; Miró, Manuel

    2014-09-01

    A novel biomimetic extraction procedure that allows for the in-line handing of ≥400 mg solid substrates is herein proposed for automatic ascertainment of trace element (TE) bioaccessibility in soils under worst-case conditions as per recommendations of ISO norms. A unified bioaccessibility/BARGE method (UBM)-like physiological-based extraction test is evaluated for the first time in a dynamic format for accurate assessment of in-vitro bioaccessibility of Cr, Cu, Ni, Pb and Zn in forest and residential-garden soils by on-line coupling of a hybrid flow set-up to inductively coupled plasma atomic emission spectrometry. Three biologically relevant operational extraction modes mimicking: (i) gastric juice extraction alone; (ii) saliva and gastric juice composite in unidirectional flow extraction format and (iii) saliva and gastric juice composite in a recirculation mode were thoroughly investigated. The extraction profiles of the three configurations using digestive fluids were proven to fit a first order reaction kinetic model for estimating the maximum TE bioaccessibility, that is, the actual worst-case scenario in human risk assessment protocols. A full factorial design, in which the sample amount (400-800 mg), the extractant flow rate (0.5-1.5 mL min(-1)) and the extraction temperature (27-37°C) were selected as variables for the multivariate optimization studies in order to obtain the maximum TE extractability. Two soils of varied physicochemical properties were analysed and no significant differences were found at the 0.05 significance level between the summation of leached concentrations of TE in gastric juice plus the residual fraction and the total concentration of the overall assayed metals determined by microwave digestion. These results showed the reliability and lack of bias (trueness) of the automatic biomimetic extraction approach using digestive juices.

  7. Determination of La,Mg in Co-based alloys by inductively coupled plasma atomic emission spectrometry%ICP-AES法测定钴基合金中La、Mg元素的含量

    Institute of Scientific and Technical Information of China (English)

    高颂; 庞晓辉; 许维兵

    2014-01-01

    A method for determination of principal elements lanthanum and magnesium in Co-based al-loys by inductively coupled plasma atomic emission spectrometry is proposed .In this method ,the micro-wave digestion is used to reduce the background .Matrix-matching method is used to eliminated spectral interference .The experiments of instrument parameters ,sample dissolution ,selection of analysis lines , and the effect of matrix on the determination ,and the comparison of reference materials and the analytical results are carried out .T he recovery rate is at the range of 90%-99% ,RSD≤4% .%研究了钴基合金样品的溶解方法,采用盐酸、硝酸、氢氟酸溶解,使用微波消解溶解方法,控制试剂用量,降低了空白;考察了基体和主量元素对待测元素的影响,选择待测元素灵敏度高、光谱干扰少的谱线 La 408.672nm、Mg 279.553nm为分析线,校准曲线溶液采用基体匹配消除了基体效应影响,实现了用电感耦合等离子体原子发射光谱法测定钴基合金中La、Mg元素含量,方法的检出限可达0.002μg/mL ,进行了标准物质对照试验,与标准值相符,进行了加入回收试验,回收率90~99%,RSD<4%。

  8. 电感耦合等离子体原子发射光谱法测定炼锑泡渣中碲%Determination of tellurium in refined antimony slag by inductively coupled plasma atomic emission spectrometry

    Institute of Scientific and Technical Information of China (English)

    张忠亭; 邓飞跃; 蒋苏琼; 刘逸群; 李彪

    2011-01-01

    建立了用电感耦合等离子体原子发射光谱法(ICP-AES)测定炼锑泡渣中碲的方法.选择波长为214.281 nm的谱线作为碲的分析线,只有La 214.281 nm,V 214.274 nm,Pt214.250 nm,Nb 214.291 nm和Re 214.297 nm线有干扰,但炼锑泡渣中La、V、Pt、Nb、Re含量都很低,其影响可以忽略,因此不需要进行预分离,样品用王水溶解后可直接进行ICP-AES测定.考察了仪器工作参数对测定结果的影响,并确定了最佳工作条件:观测高度为15 mm,雾化气流速为0.8 L/min,射频功率为1 300 W.方法线性范围为0.01~100 mg/L,线性相关系数为1.000 0,检出限(3σ)为0.007 2 mg/L,样品测定结果的相对标准偏差(RSD)为0.16%,加标回收率为97%~102%.%The determination method of tellurium in refined antimony slag by inductively coupled plasma atomic emission spectrometry (ICP-AES) was established. The spectral line of 214. 281 nm was used as the analytical line of tellurium. Only La 214. 281 nm, V 214. 274 nm, Pt 214. 250 nm, Nb 214. 291 nm and Re 214. 297 nm lines had interference. However, the content of La, V, Pt, Nb and Re in refined antimony slag were very low, so their influence could be ignored and the pre-separation was not necessary. After dissolving with aqua regia, the sample solution was directly determined by ICP-AES. The effect of instrumental working parameters on determination results was investigated. The optimal working conditions were as follows: observation height, 15 mm; flow rate of atomizing gas, 0.8 L/min; radio frequency power, 1 300 W. The linear range of method was 0. 01-100 mg/L with correlation coefficient of 1. 000 0. The detection limit (3a) was 0. 007 2 mg/L. The relative standard deviation (RSD) was 0. 16 %, and the recoveries of standard addition were 97 %-102 %.

  9. 电感耦合等离子体发射光谱法测定油田水中的硼%Determination of Boron in Oil Field Water by Inductively Coupled Plasma-Atomic Emission Spectrometry

    Institute of Scientific and Technical Information of China (English)

    宋继芳

    2012-01-01

    样品经硝酸酸化、滤膜过滤处理后,用电感耦合等离子体发射光谱法直接测定其中硼的含量.通过正交实验优选仪器参数和分析谱线,在选定的波长208.959nm下,对样品稀释倍数和介质酸种类进行选择,结果表明,硼含量低于10mg/L的样品不用稀释,高于10mg/L的样品一般稀释20倍,介质选用硝酸可使测定结果更加准确.对油田水中共存的7种主要金属元素进行了干扰试验,样品中存在20mg/L的Sr、Ba、Fe,50mg/L的Mg、Ca,100mg/L的K,200mg/L的Na对待测元素的测定没有影响.选取油田水样品进行加标回收试验,方法平均回收率为95.3%~102.0%,精密度(RSD,n=11)为0.43%~0.92%,检出限为0.0020mg/L.方法简便、快速,结果令人满意,与姜黄素分光光度法比较,克服了分析流程长、使用试剂较多且不易操作的不足.%Boron in oil field water has been directly determined by Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) after sample were treated with nitric acid and filtrated. This method overcomes the problems of spectrophotometry such as long analysis flow, more reagent and difficulty in controlling the chemical procedure. The working parameters and the spectral line were optimized by orthogonal tests. The dilute multiple and acid medium were analyzed using the selected 208.959 nm frequency. The results show that it is not necessary to dilute the sample when the content of B is less than 10 mg/L, and the dilution factor is 20 when B is greater than 10 mg/L. The selected HNO3 as the acid medium, improved the accuracy of the results. The interference tests were carried out for 7 major metals in oil field water. 20 mg/L Sr, Ba and Fe, 50 mg/L Mg and Ca, 100 mg/L K and 200 mg/L Na have no interference for the measurements of the target element. The detection limit of boron was 0.0020 mg/L and the recoveries ranged from 95.3% to 102.0% with a precision in the range of 0.43% - 0.92% ( RSD, n = 11

  10. THz Emission Spectroscopy for THz Spintronics

    Science.gov (United States)

    Jarik Huisman, Thomas; Rasing, Theo

    2017-01-01

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

  11. A novel method for simultaneous determination of selected elements in dolomite and magnesia by Inductively Coupled Plasma Atomic Emission Spectroscopy with slurry sample introduction

    Science.gov (United States)

    Bok-Badura, Joanna; Jakóbik-Kolon, Agata; Turek, Marian; Szczerba, Jacek; Lemanowicz, Marcin; Karoń, Krzysztof

    2015-11-01

    The slurry nebulization ICP-AES method for simultaneous determination of selected elements in dolomite and magnesia was proposed. Based on the investigation results the optimal conditions for this analysis were as follows: particle size CRM 782-1 and High Purity Magnesia BCS-CRM 389/1 were analyzed. Student's t-test proved that there were no statistically significant differences between determined values and the certified ones. This proves that the slurry sample introduction into plasma in ICP-AES technique can be applied for simultaneous determination of elements in dolomite and magnesia.

  12. Mid infrared emission spectroscopy of carbon plasma

    Science.gov (United States)

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

    2017-01-01

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

  13. Mid infrared emission spectroscopy of carbon plasma.

    Science.gov (United States)

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

    2017-01-05

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

  14. Determination of Trace Elements in Pomegranate Peel and Pomegranate Seed by Inductively Coupled Plasma-Atomic Emission Spectrometry with Microwave Digestion%微波消解-等离子体原子发射光谱法测定石榴皮和石榴籽中微量元素

    Institute of Scientific and Technical Information of China (English)

    吴佳; 解成喜

    2012-01-01

    采用微波消解样品,电感耦合等离子体原子发射光谱法(ICP-AES)测定了石榴皮和石榴籽中K、Ca、Mg、Fe、A1、Cu、Zn、Mn、Na、Li、P、S12种微量元素的含量.在最佳仪器工作条件下,各元素的加标回收率为91.8%~103.1%,相对标准偏差(RSD)为0.70%~2.68%.实验结果可为石榴皮和石榴籽中微量元素与其药效的相关性提供科学依据.%The trace elements of K,Ca,Mg,Fe, Al,Cu,Zn,Mn,Na,Li,P and S in the pomegranate peel and pomegranate seed were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) with microwave digestion. Under the optimal working conditions of the equipment, the element recoveries of standard addition are 91. 8% ~ 103. l%,and the relative standard deviations (RSDs) are 0. 70%~2. 68%.

  15. Determination of Twelve Trace Elements in Children`s hair by Inductively Coupled Plasma Atomic Emission Spectrometry%电感耦合等离子体发射光谱法测定儿童发样中十二种微量元素

    Institute of Scientific and Technical Information of China (English)

    代建强; 杨诗佳

    2013-01-01

    This paper uses the nitric acid and hydrogen peroxide sample digestionarticle, Determination of aluminum, calcium, chromium, copper, iron, potassium, magnesium, sodium, manganese, lead, nickel, zinc and other trace elements in children's hair by inductively coupled plasma atomic emission spectrometry.The recovery rate of 95%~105%,The detection limit of element (ug/ml) in 0.0010-0.011,The relative standard deviation (RSD, n=9) is less than 4%,After verification of human hair in national standard reference samples, The measured value had no significant difference with standard value.%采用硝酸-过氧化氢消解试样,电感耦合等离子体发射光谱法测定儿童发样中铝、钙、铬、铜、铁、钾、镁、锰、钠、铅、镍、锌等十二种微量元素。方法回收率95%~105%,各元素检出限(ug/mL)在0.0010~0.011之间,相对标准偏差(RSD,n=9)小于4%,经人发国家一级标准物质验证,测定值与标准认定值无明显差异。

  16. 电感耦合等离子体发射光谱法测定镍矿石中镍铜铅锌%Determination of Ni,Cu,Pb and Zn in nickel ores by inductive coupling plasma-atomic emission spectrometry

    Institute of Scientific and Technical Information of China (English)

    郭爽; 金震宇; 杨婷; 于微

    2012-01-01

    The authors dissolved the sample of the nickle ore with hydrofluoric acid,nitric acid,hydrochloric acid and high chloride acid.Dissolved the salt with aqua regia.To determine the elements of nickel,copper,lead and zinc in the solution by inductive coupling plasma-atomic emission spectrometry,to interfere survey the target elements in spectrum lines,and to select the suitable analytical spectral lines.The result of the experiment proves that the nickel can increase the spectrum line background and overlapping peak of the target elements,In addition,the recovery rate ranges from 98% to 103%,and the relative deviation less than 3.%选用氢氟酸、硝酸、盐酸、高氯酸对镍矿石样品进行溶样,用王水溶解盐类,电感耦合等离子体发射光谱法测定溶液中镍、铜、铅、锌元素,对目标元素进行谱线干扰考察,选择合适的分析谱线,结果表明镍会使目标元素谱线背景和叠加峰轻度增高,回收率都在98%~103%,相对偏差小于3。

  17. Determination of Fe_2O_3,TiO_2 and SiO_2 in bauxite by inductivelycoupled plasma-atomic emission spectrometry%ICP-AES法测定矾土中Fe2O3、TiO2和SiO2

    Institute of Scientific and Technical Information of China (English)

    郝荷芳; 苑利

    2011-01-01

    采用四硼酸锂熔融试样,电感耦合等离子体原子发射光谱法(ICP-AES法)测定矾土中Fe2 O3、TiO2和SiO2。通过对熔样方法选择、铝基体以及背景的研究,确定了分析条件。结果表明,该法具有良好的精密度和准确性,回收率在94%~108%。%A method based on inductively coupled plasma-atomic emission spectrometry(ICP-AES) was established for the determination of Fe2O3,TiO2 and SiO2 in bauxite.The sample was melted into lithium tetraborate.The analysis conditions were obtained by studying the melted methods,Al matrix and background.The recommended method showed satisfying precision and accuracy as well.The recovery percents detected by standard addition method were in range of 94%~108%.

  18. Speciation analysis of triethyl-lead and tributyl-tin compounds in human urine by liquid-liquid extraction and gas chromatography microwave-induced plasma atomic emission detection.

    Science.gov (United States)

    Zachariadis, George A; Rosenberg, Erwin

    2012-05-01

    This work describes the development of a fast method for speciation analysis of triethyl-lead and tributyl-tin species in urine samples after in situ derivatization by tetraethyl- or tetrapropyl-borate reagents. The alkylation reaction is done in the aqueous and urine medium and the less-polar derivatives are extracted in hexane by liquid-liquid extraction. The species were extracted and the extract was efficiently collected from the aqueous phase after centrifugation. Finally, the organometallic species are separated by gas chromatography and determined from the emission signals of elemental lead and tin. Atomic lead and tin are formed from the organolead and organotin compounds during atomization of the column eluate in a microwave-induced helium plasma source. The simultaneous measurement of lead (Pb) at 405.780 nm and tin (Sn) at 303.419 nm was achieved by an atomic emission detector. Finally, the analytes were determined with satisfactory precision (urine is extracted with 1 mL of hexane and 1 μL of extract is injected.

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

    Science.gov (United States)

    Schlagen, Kenneth J.

    1992-01-01

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

  20. Determination of Serum Lithium by Flame Emission Spectroscopy

    Directory of Open Access Journals (Sweden)

    R. Nafissy

    1976-07-01

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

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

    Science.gov (United States)

    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. Determination of eight impurity elements in industrial silicon by inductively coupled plasma atomic emission spectrometry%电感耦合等离子体原子发射光谱法测定工业硅中8种杂质元素

    Institute of Scientific and Technical Information of China (English)

    张云晖; 杨晓静; 亢若谷; 赵建为; 金波

    2013-01-01

    The inert sample injection system resistant hydrofluoric acid of inductively coupled plasma atomic emission spectrometer was used. The sample solution was injected directly without removing hydrofluoric acid and silicon matrix after sample was dissolved in hydrofluoric acid, nitric acid and perchloric acid. Eight impurities including iron, aluminum, calcium, titanium, manganese, nickel, boron and phosphorus in industrial silicon powder were simultaneously determined by inductively coupled plasma atomic emission spectrometry (ICP-AES). Most of matrix silicon had been volatilized and removed in sample dissolution process, so the matrix effect had no influence on the determination of i-ron, aluminum, calcium, titanium, manganese and nickel. However, the determination of boron and phosphorus was still affected, which could be eliminated by vertical observation method. The detection limit of the method was calculated by three times of standard deviation of blank. The detection limits (w/%) for iron, aluminum, calcium, titanium, manganese, nickel, boron and phosphorus were 0. 004, 0. 001, 0. 004, 0. 001, 0. 0001, 0. 0001, 0. 000 04 and 0. 000 06, respectively. The proposed method was applied to the determination of eight impurities in industrial silicon. The found results were consistent with the certified values or those obtained by standard method (GB/T 14849. 4-2008).%采用电感耦合等离子体原子发射光谱仪的耐氢氟酸惰性进样系统,在样品用氢氟酸、硝酸、高氯酸溶解完全后无需赶尽氢氟酸和硅基体,直接进样,电感耦合等离子体原子发射光谱法同时测定了工业硅粉中铁、铝、钙、钛、锰、镍、硼和磷8种杂质元素.因为在溶样过程中大部分基体硅已挥发除去,基体效应对铁、铝、钙、钛、锰、镍的测定没有影响,但是对硼和磷的测定仍有影响,这种影响可以采用垂直观测方式克服.按照空白值的3倍标准偏差计算方法的检测限,得到

  3. 电感耦合等离子体原子发射光谱法同时测定饮用水的硬度和碱度%Simultaneous determination of the hardness and alkalinity in drinking water by inductively coupled plasma atomic emission spectrometry

    Institute of Scientific and Technical Information of China (English)

    霍建中; 段旭川

    2013-01-01

    The feasibility of simultaneous determination of hardness and alkalinity of drinking water by inductively coupled plasma atomic emission spectrometry (ICP-AES) was studied.the water sample was acidified off-line with diluted hydrochloric acid.The bicarbonates in water sample were in-situ converted into carbon dioxide,which was also dissolved in original water.Then,the solution was sampled by conventional single tube of inductively coupled plasma atomic emission spectrometer.The simultaneous sampling of CO2,Ca and Mg was realized at relatively low atomizer pressure.Among them,CO2 was sampled in gas state,while Ca and Mg were sampled in atomizing state.In this study,the bicarbonates with low sampling efficiency in atomizing method were converted into gas carbon dioxide,which had high sampling efficiency,thus the determination sensitivity of carbon was increased,realizing the accurate determination.The measured content of inorganic carbon was converted to the content of bicarbonates,so the alkalinity of drinking water was obtained.Meanwhile,the content of Ca and Mg was converted to the content of calcium carbonate to calculate the hardness of water.Under the optimal experimental conditions,i.e.,atomizer pressure of 241.3 kPa and dilution ratio of 5for water sample,the hardness and alkalinity of drinking water were simultaneously determined by this method.The found results were consistent with those obtained by titration method.%研究了使用电感耦合等离子体原子发射光谱法(ICP-AES)同时测定饮用水的硬度和碱度可行性.通过用稀盐酸离线酸化水样,使水样中的碳酸氢根原位转化为二氧化碳并继续溶解在原水中,然后使用ICP-AES仪器上常规的单管吸取溶液,在比较低的雾化器压力下实现了CO2、Ca、Mg的同时进样.其中CO2属于气态进样,而钙、镁属于雾化进样.由于方法将雾化法进样效率低的碳酸氢根转化成进样效率高的二氧化碳气态,因此碳的测定灵敏

  4. Determination of Heavy Metals in Electroplating Sludge Leaching Liquid by Inductively Coupled Plasma Atomic Emission Spectrometry%电感耦合等离子体原子发射光谱法测定电镀污泥浸出液中的重金属

    Institute of Scientific and Technical Information of China (English)

    徐国津; 樊颖果; 赵倩

    2014-01-01

    Heavy metals in electroplating sludge leaching liquid such as Cu,Zn,Ni,Cr,Pb,Cd and Ba were determined by inductively coupled plasma atomic emission spectrometry with sulfuric acid-nitric acid extraction. The working conditions of the instrument and interference factors and elimination method were studied. Under the selected conditions,the linear correlation coefficients were all 0.999 9,the detection limits were between 0.002 mg/L and 0.01 mg/L,recoveries ranged from 93.5%to 106.0%,and the relative standard deviations of determination results were less than 10%(n=6). The method could quickly and accurately detect some heavy metals in electroplating sludge leaching liquid.%采用硫酸-硝酸溶液浸提电镀污泥中的重金属,建立电感耦合等离子体原子发射光谱法(ICP-AES)测定电镀污泥浸出液中铜、锌、镍、铬、铅、镉、钡元素的分析方法。研究了仪器的工作条件及影响检测方法的干扰因素和消除。在选定的条件下,线性相关系数均为0.9999,检出限为0.002~0.01 mg/L,加标回收率为93.5%~106.0%,测定结果的相对标准偏差小于10%(n=6)。该方法准确快速,可用于电镀污泥浸出液中多种重金属的含量测定。

  5. 电感耦合等离子体原子发射光谱法测定新疆洋葱籽中常量/微量元素%Determination of Major/Trace Elements in the Xinjiang Allium cepa L.Seeds by Inductively Coupled Plasma Atomic Emission Spectrometry

    Institute of Scientific and Technical Information of China (English)

    孙凤; 邓丽霜; 童红; 王强

    2013-01-01

    Six samples were pretreated by microwave digestion method and analyzed by inductively coupled plasma atomic emission spectrometry (ICP-AES). And 18 kinds of major/trace elements in Xinjiang Allium cepa L. seeds were determined including Co, Cr, Ca, K, Mg, P, Fe, Mn, Na, Ni, Sn, Zn, Cd, As,Se, Cu, Mo and V. Results indicated that Allium cepa L. seeds were riched in major elements such as K,Mg,P,Ca and Na, besides, the trace elements Fe, Mn,Zn,Cr,Ni,and Cu were also relatively abundant. Allium cepa L. seeds contain a lot of major and trace elements which are beneficial to human body and have high medicinal value.%采用微波消解法处理样品,以电感耦合等离子体原子发射光谱法(ICP AES)测定新疆洋葱籽样品中Co、Cr、Ca、K、Mg、P、Fe、Mn、Na、Ni、Sn、Zn、Cd、As、Se、Cu、Mo和V 18种常量/微量元素.结果显示,新疆洋葱籽中含有丰富的K、Mg、P、Ca和Na等常量元素,此外微量元素Fe、Mn、Zn、Cr、Ni、Cu的含量也较丰富.新疆洋葱籽中含有很多对人体有益的常量及微量元素,有较高的药用价值.

  6. Spectroscopy of unusual emission-line stars

    Science.gov (United States)

    Bopp, Bernard W.

    1988-01-01

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

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

    Science.gov (United States)

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

    2009-03-01

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

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

    Science.gov (United States)

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

    2007-04-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-04-15

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

  10. Determination of Chromium,Zirconium,Vanadium and Hafnium in Polyethylene and Polypropylene by Inductively Coupled Plasma Atomic Emission Spectrometry%电感耦合等离子体原子发射光谱法测定聚乙烯、聚丙烯中铬、锆、钒和铪

    Institute of Scientific and Technical Information of China (English)

    陈金凤; 陈章捷; 钟坚海; 郑宗展

    2011-01-01

    采用微波消解技术对以聚乙烯、聚丙烯为原料制作的食品容器、食品包装薄膜进行预处理,确定了溶样酸介质及其用量、微波消解温度、时间等关键因素,建立了一种快速测定聚乙烯、聚丙烯材料中铬、锆、钒和铪含量的电感耦合等离子体原子发射光谱法。实验结果表明,5mL硝酸和1mL过氧化氢的混合溶液即可实现样品的完全消解,同时通过优化光谱分析条件,得到铬、锆、钒和铪的检测限分别为1.0 mg/kg,0.7mg/kg,0.7 mg/kg,1.4 mg/kg。该法加标回收率在88%-103%之间,相对标准偏差(n=3)为0.84-6.4%。用于实际样品的测定,所得结果与标准样品的参考值相符。%A method for the rapid determination of chromium,zirconium,vanadium and hafnium in polyethylene and polypropylene by inductively coupled plasma atomic emission spectrometry was established.The samples made of polyethylene and polypropylene used as food container or food wrapper was pretreated by microwave digestion.The effects of digestion media and it's use amount,digestion temperature and holding time on digestion results were investigated.It was experimentally indicated that the samples could be thoroughly digested in a mixture of 5 mL of nitric acid and 2 mL of hydrogen peroxide.Under the optimal conditions,the detection limits of chromium,zirconium,vanadium and hafnium were 1.0 mg/kg,0.7 mg/kg,0.7 mg/kg and 1.4 mg/kg respectively.The recoveries of standards in polyethylene and polypropylene samples were from 88% to 103%,with the RSDs of 0.84%-6.4%(n=3).This method was employed in the determination of real samples,the analytical results was accorded with the certified results.

  11. 碱熔融电感耦合等离子体原子发射光谱法测定生铁中硅锰磷含量%Determination of Silicon Manganese and Phosphorus in Pig Iron with Inductively Coupled Plasma Atomic Emission Spectrometry

    Institute of Scientific and Technical Information of China (English)

    吴金龙; 金献忠

    2014-01-01

    A method was proposed for the determination of silicon, manganese, and phosphorus in pig iron with inductively coupled plasma atomic emission spectrometry . Samples were fused with sodium hydroxide and sodium peroxide in zirconium crucibles and leached out with hydrochloric acid solution. The matrix effect were investigated, no effect on the measured elements by sodium between 5.0 mg/mL and 6.0 mg/mL, zirconium in 20μg/mL and other elements in pig iron was found. Acidity effect was discussed and the effect of the volume of hydrochloric acid between 8 percent and 12 percent was able to be ignored. CRMs of pig iron were analyzed, and good agreements were achieved on the detected levels and the certified values with RSDs (n=5) being in the range of 0.3%-1.0%.%提出了一种电感耦合等离子体原子发射光谱法测定生铁中硅、锰、磷含量的方法。生铁样品采用氢氧化钠和过氧化钠在锆坩埚内熔融,盐酸浸取;研究了共存元素的影响,浓度在5.0 mg/mL-6.0 mg/mL之间的钠元素、20μg/mL的锆元素以及样品中其他共存元素对各元素的测定结果无影响;考察了酸度效应,盐酸用量在体积分数8%-12%时,对各元素测定的影响可以忽略。以生铁标准物质作为样品进行分析,测定值和认定值相吻合,RSD(n=5)为0.3%-1.0%。

  12. Determination of phosplorus, nickel, copper, titanium and vanadium in ferromanganese by microwave digestion-inductively coupled plasma atomic emission soectrometry%微波消解—电感耦合等离子体发射光谱法测定锰铁中磷镍铜钛钒

    Institute of Scientific and Technical Information of China (English)

    赵容超; 李海平; 杨大蔚; 井婷婷

    2012-01-01

    锰铁样品经微波消解后,选择327.395、231.604、177.434、334.941、309.310 nm波长的光谱线分别作为铜、镍、磷、钛、钒的分析线,用电感耦合等离子体发射光谱法测定了锰铁样品中铜、镍、磷、钛、钒含量.基体锰产生的基体效应可以通过基体匹配的方法消除,基体铁对测定没有影响.方法用于测定锰铁标样,测定值与认定值一致;用于测定锰铁试样,测定结果的相对标准偏差在0.2%0~3.6%o之间,加标回收率为97%~103%.方法可以用于中、高、低碳锰铁中铜、镍、磷、钛、钒的测定.%After pretreatment with microwave digestion and selection of spectral lines at the wavelength of 327. 395,231. 604,177. 434,334. 941 and 309. 310 nm as the analytical line of copper, nickel, phosphorus, titanium and vanadium, respectively, the content of copper, nickel, phosphorus, titanium and vanadium in ferromanganese sample was determined by inductively coupled plasma atomic e-mission spectrometry. The matrix effect produced by matrix manganese could be eliminated by matrix matching while the matrix iron did not have influence on the determination. When the method was applied to determine ferromanganese certified reference materials, the determination results were the same as the certified values. When it was applied to determine ferromanganese actual samples, relative standard deviations of the determination results were between 0. 2% and 3. 6% and recoveries were between 97% and 103%. The method could be used to determine copper, nickel, phosphorus, titanium and vanadium in the medium, high and low-carbon ferromanganese.

  13. 碱熔—电感耦合等离子体原子发射光谱法测定红土镍矿中硅钙镁铝锰钛铬镍钴%Determination of silicon, calcium, magnesium, aluminium, manganese,titanium, chromium, nickel and cobalt in laterite nickel ore by alkali fusion-inductively coupled plasma atomic emission spectrometry

    Institute of Scientific and Technical Information of China (English)

    高亮

    2013-01-01

    The determination method of nine elements (silicon, calcium, magnesium, aluminium, manganese, titanium, chromium, nickel and cobalt) in laterite nickel ore by inductively coupled plasma atomic emission spectrometry (ICP-AES) was established. The laterite nickel ore sample was fused by anhydrous Na2CO3-H3BO3 mixed flux, then acidified and leached by hydrochloric acid. The high salt atomizer and cyclone chamber were used. Under the selected measurement conditions, the content of nine elements in sample solution was determined by ICP-AES. The influence of salts introduced by matrix iron and sample treatment could be eliminated by matrix matching method. The precision test results showed that, the relative standard deviations (RSD) of elements were smaller than 5 %. The proposed method was applied to the determination of reference material, and the determination results of nine elements were basically consistent with the certified values.%建立了红土镍矿中Si、Ca、Mg、Al、Mn、Ti、Cr、Ni、Co 9种元素的电感耦合等离子体原子发射光谱测定方法.红土镍矿样品用无水Na2CO3-H3BO3混合熔剂熔融,盐酸浸取、酸化,选用高盐雾化器和旋流雾室,在选定的测量条件下,用电感耦合等离子体原子发射光谱法测定试液中9种元素含量.基体铁和处理样品时引入试液中的盐分对测定的影响可以通过基体匹配的方法消除.精密度试验结果表明,样品中各元素测定结果的相对标准偏差小于5%.用本法测定标准样品,9种元素的测定值与认定值基本一致.

  14. Affirmation of the Method that Simultaneous Determination of Copper, Lead, Zinc, Cobalt and Nickel in Copper, Lead and Zinc Ores by Inductively Coupled Plasma-Atomic Emission Spectrometry%电感耦合等离子体发射光谱法同时测定铜铅锌矿石中铜铅锌钴镍等元素方法确认

    Institute of Scientific and Technical Information of China (English)

    熊英; 王晓雁; 胡建平

    2011-01-01

    文章在修订GB/T 14353-1993研究工作中,建立了电感耦合等离子体发射光谱同时测定铜铅锌矿石中铜铅锌钴镍等元素的标准分析方法.通过控制试样量和制备试样溶液的体积,可实现主量元素铜、铅、锌与次量元素钴、镍的同时测定.测定范围为铜0.002%~8.5%,铅0.01%~5%,锌0.005%~3%,钴0.001 5%~0.5%,镍0.003%~0.5%.按照相关国家标准对测量方法与结果的准确度进行8个实验室协同参加的准确度试验,统计参数结果表明在限定水平范围内方法偏倚不显著;利用方法重复性限参数,计算可能产生的最大相对偏差.分析方法精密度满足的要求.%A standard analysis method for simultaneous detecting copper, lead, zinc, cobalt, nickel and other elements by inductively coupled plasma-atomic emission spectrometry (ICP-AES) was developed when improving GB/T 14353-1993 , the method for chemical analysis of copper ore, lead ore and zinc ore. The major elements such as copper, lead, zinc and the minor elements of cobalt and nickel can be simultaneous detected by adjusting the test portion amounts and reagent solution volumes. The determination ranges of copper, lead, zinc, cobalt and nickel are respectively 0.002% -8.5% , 0. 01% - 5% , 0. 005% - 3% , 0. 001 5% - 0. 5% and 0. 003% - 0. 5%. According to relevant national standards, this method was tested by eight cooperation laboratories. Statistical results indicated that the method is impartial within a definitive range. The repeatability limit parameter was used to calculate the possible maximum deviations. The precision of the method satisfied the requirement of "The specification of testing quality management for geological laboratoris".

  15. 电感耦合等离子体发射光谱法测定红土镍矿中镍钻铜%Determination of Ni, Co and Cu in Laterite-Nickel Ores by Inductively Coupled Plasma-Atomic Emission Spectrometry

    Institute of Scientific and Technical Information of China (English)

    王国新; 许玉宇; 王慧; 刘烽; 吴骋; 胡清

    2011-01-01

    A method for the determination of Ni, Co and Cu contents in laterite is presented in this paper. Laterite samples were fused with a mixed flux of Na2CO3-Na2B4O7, then the analytes were extracted by HC1 acid. The sample solution was measured by inductively coupled plasma-atomic emission spectrometry (ICP-AES). The internal standard method was used to avoid matrix interference based on choosing Y 371. 030 nm as the internal calibration line for Cu (324.754 nm) and Y 224.306 nm for Ni (231.604 nm) and Co (228.616 nm). The detection limits for Ni, Co and Cu were 0. 5 μg/g, 1.0 μg/g and 1.0 μg/g, respectively. The relative standard deviations (RSD) of the test result were 1. 2% -2. 0% (n =7) , and the recoveries ranged from 95% to 103.6%, which met the requirements of analysis for laterite.%红土镍矿样品用无水Na2 CO3 - Na2 B4 O7混合熔剂熔融,HCl浸出酸化,电感耦合等离子体发射光谱法直接测定样品中镍、钴、铜的含量.Cu 324.754 nm使用Y 371.030 nm作为内标线,Ni 231.604 nm、Co 228.616 nm使用Y 224.306 nm作为内标线校正基体干扰,方法检出限镍为0.5μg/g、钴为1.0 μg/g、铜为1.0μg/g,相对标准偏差( RSD,n=7)为1.2% ~2.0%,加标回收率为95.0% ~ 103.6%,能满足红土镍矿的分析要求.

  16. Methods of Cold Soaking, Foam Plastics Enrichment and Inductive Coupling Plasma Atomic Emission Spectrometry%冷浸取--泡塑富集-电感耦合等离子体发射光谱法测定化探样品中的超痕量金铂钯研究

    Institute of Scientific and Technical Information of China (English)

    闵慧英; 袁蕙霞; 郭玉翠

    2015-01-01

    建立了冷浸--泡沫塑料富集,采用 ICP-AES 测定地球化学勘探样品中超痕量金、铂、钯的方法,并试验了冷浸取、泡沫塑料富集时各种因素的影响;确定了采用氯化钠、盐酸和高锰酸钾冷浸取分解试样,以泡沫塑料富集、灰化,残渣用王水溶解,用电感耦合等离子体发射光谱法测定的条件。该方法检出限分别为:Au 0.039ng/g,Pt 0.040ng/g,Pd 0.058ng/g;回收率为95.6%~102.5%之间;测量精密度( RSD%)为:Au 4.85%,Pt 5.76%,Pd 6.45%。采用该方法测定了国家一级地球化学标准物质中的痕量 Au,Pt,Pd,测定值与标准值符合规范要求。%In this paper, we set up the enrichment of cold soaking foam plastics by adopting the method of ICP-AES to test the ultra-trace of gold, platinum and palladium from the geochemical exploration sample and studied all kinds of effective factors in cold soaking foam plastics enrichment. And we confirmed the requirements of using sodi-um chloride, hydrochloric acid and potassium permanganate cold soak-ing to decompose the sample, using foam plastics to enrich and ash, aqua regia to dissolve residue, and measuring by inductive coupling Plasma Atomic Emission Spectrometry. The detection limits of this method are as follows: detection limit: Au 0.039ng/g, Pt 0.040ng/g, Pd 0.058ng/g; recovery rate: between 95.9% and 102.2%; relative stan-dard deviation (RSD%): Au 4.85%,Pt 5.76%,Pd 6.45%.We tested the trace amount of Au, Pt and Pd in the country-level geochemistry stan-dard substance. The measured value is consistent with the normalized value.

  17. 电感耦合等离子体原子发射光谱法测定镍基钎焊料中铬和硅%Determination of chromium and silicon in nickel-based brazing material by inductively coupled plasma atomic emission spectrometry

    Institute of Scientific and Technical Information of China (English)

    杨丽; 王金阳; 张庸

    2013-01-01

    The analysis conditions of chromium and silicon in nickel-based brazing material by inductively coupled plasma atomic emission spectrometry (ICP-AES) were discussed.After the nickelbased brazing material was dissolved with aqua regia-hydrofluoric acid mixed acid,and matrix effect was reduced by matrix matching,chromium and silicon in the sample were determined by ICP-AES with spectral line of 267.716(125) nm and 251.612(133) nm as the analytical lines for chromium and silicon respectively.This proposed method was applied to the determination of chromium and silicon in actual samples and the results were consistent with those obtained by ammonium persulfate oxidization titration method and perchloric acid dehydration method.The relative standard deviation (RSD,n =6) of chromium and silicon was 0.55%-0.73% and 0.71%-1.0%,respectively.The recoveries were 100%-101% and 99%-100%,respectively.%探讨了电感耦合等离子体原子发射光谱法(ICP-AES)测定镍基钎焊料中铬和硅的分析条件.试样经王水和氢氟酸混合酸溶解,选择267.716(125) nm和251.612(133) nm的光谱线分别作为铬和硅的分析线,并采用基体匹配法降低了基体效应,ICP-AES测定了镍基钎焊料中铬和硅含量.实际样品中铬和硅的测定结果与过硫酸铵氧化滴定法和高氯酸脱水法相符,铬和硅的相对标准偏差(n=6)分别为0.55%~0.73%和0.71%~1.0%,加标回收率分别为100%~101%和99%~100%.

  18. Plant species discrimination using emissive thermal infrared imaging spectroscopy

    Science.gov (United States)

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

    2016-12-01

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

  19. Elemental speciation analysis by multicapillary gas chromatography with microwave-induced plasma atomic spectrometric detection.

    Science.gov (United States)

    Rodriguez Pereiro, I; Schmitt, V O; Lobiński, R

    1997-12-01

    Multicapillary column gas chromatography (MC-GC)/microwave-induced plasma atomic emission spectrometry (MIP AES) was developed for fast speciation analysis of organotin compounds in the environment. Ethylated butyltin compounds could be separated isothermally within less than 30 s (instead of ∼5-10 min) without sacrificing either the resolution or the sample capacity of conventional capillary GC with oven temperature gradient programming. Careful optimization of the pressure and temperature GC program allowed a comprehensive organotin speciation analysis including phenyltin compounds within less than 2.5 min, increasing the sample throughput 6-fold. Compatibility of MC-GC with an MIP atomic emission detector (MIP-AED) was discussed. MC-GC/MIP-AES was validated for the analysis of sediment (PACS-1 and BCR 462) and biological (NIES11) certified reference materials.

  20. Spectroscopy of an unusual emission line M star

    Science.gov (United States)

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

    1991-01-01

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

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

    Directory of Open Access Journals (Sweden)

    Ana Rei

    2012-01-01

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

  2. Emission Line Imaging and Spectroscopy of Distant Galaxies

    DEFF Research Database (Denmark)

    Zabl, Johannes Florian

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Spencer, W.A.

    2000-07-27

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

  4. Current Problems in X-Ray Emission Spectroscopy

    Science.gov (United States)

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

    1989-01-01

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

  5. Determination of elements in tea seeds by inductively coupled plasma atomic emission spectrometry%电感耦合等离子体发射光谱(ICP-OES)法快速测定茶叶籽中多种元素

    Institute of Scientific and Technical Information of China (English)

    董海胜; 臧鹏; 王妮; 黄贱英

    2014-01-01

    Objective To analyze the etal elements in tea seed, so as to provide a reference for tea seed utilization. Methods Rapid quantitative analysis for elements As, Ca, Cd, Cr, Cu, Fe, K, Mg, Mn, Na, Pb, Se and Zn in tea seeds was carried out by the high-pressure sealed microwave digestion combined with inductively coupled plasma atomic emission spectrometry. Results The content of each element in tea seed were as fol-lowing:Mg (1652.23 mg/kg), Ca (1 026.36 mg/kg), Mn (122.44 mg/kg), Na (37.77 mg/kg) , Cr (7.58 mg/kg), Cu (9.11 mg/kg), Fe (58.17 mg/kg), Zn (17.59 mg/kg) and K (9191.29 mg/kg), while, As, Cd, Pb and Se were not detected. Method recoveries for all the elements used in this research were between 89%and 113%. Con-clusion The method established in this research satisfies the analysis requirements of element in tea seed. Contents of potassium, magnesium and calcium are of high lever in tea seed, while sodium content is relatively low. Tea seed is rich in minor elements such as manganese, iron, zinc and chromium.%目的:对茶叶籽中金属元素进行分析,为茶叶籽综合利用提供参考。方法采用高压密闭微波消解结合电感耦合等离子体发射光谱法对茶叶籽中As、Ca、Cd、Cr、Cu、Fe、K、Mg、Mn、Na、Pb、Se及Zn等元素进行了同时快速定量分析。结果茶叶籽中各元素含量: Mg(1652.23 mg/kg)、Ca(1026.36 mg/kg)、Mn(122.44 mg/kg)、Na(37.77 mg/kg)、Cr(7.58 mg/kg)、Cu(9.11 mg/kg)、Fe(58.17 mg/kg)、Zn(17.59 mg/kg)、K (9191.29 mg/kg)。As、Cd、Pb及Se未检出。方法加标回收率89%~113%。结论此方法满足茶叶籽样品中所述元素的分析要求。茶叶籽中钾、镁及钙含量较高,钠含量相对较低;锰、铁、锌及铬元素含量丰富。

  6. Determination of platinum and palladium in copper leaching residue by inductively coupled plasma atomic emission spectrometry with lead fire assaying%铅试金-电感耦合等离子体原子发射光谱法测定铜浸出渣中铂钯

    Institute of Scientific and Technical Information of China (English)

    魏巍; 柴徐彬

    2015-01-01

    Platinum and palladium in copper leaching residue were captured into gold-silver composite granule by lead fire assaying method. Then, the gold-silver composite granule was dissolved with nitric acid (1+7). After the solution was pouring out, the residues were dissolved with aqua regia(1+1). Merging the solutions above, the hy-drochloric acid (1+1) was added to precipitate the silver. After filtration, the content of platinum and palladium in filtrate was determined. Thus, a method was established for determination of platinum and palladium in copper leaching residue by inductively coupled plasma atomic emission spectrometry ( ICP-AES) . The interference tests of gold and silver in gold-silver composite granule indicated that the absorption of platinum and palladium by silver chloride precipitate could be eliminated through continuous stirring in precipitation process. Meanwhile, gold in so-lution had no interference with the determination. The proposed method was applied to the determination of copper leaching residue actual samples. The relative standard deviations of the results (RSD, n=11) were 5. 6%-9. 7%, and the recoveries were between 94% and 104%. The content of platinum and palladium in control samples of cop-per leaching residue was determined by proposed method. The results were consistent with the reference values.%采用铅试金法将铜浸出渣中的铂和钯捕集于金银合粒中,用硝酸(1+7)溶解金银合粒,倾出硝酸溶解液,用王水(1+1)溶解剩余的残渣,合并两次溶解液,加入盐酸(1+1)沉淀银,过滤,对溶液中铂和钯进行测定,建立了电感耦合等离子体原子发射光谱法( ICP-AES )测定铜浸出渣中铂和钯的分析方法。金银合粒中金和银的干扰试验表明:在沉淀过程中不断搅拌可消除氯化银沉淀对铂和钯吸附的影响,同时溶液中的金对测定不产生干扰。方法用于铜浸出渣实际样品分析,测得结果的相对标准偏差(RSD,n=11)为5.6%~9.7%,

  7. Inductively coupled plasma atomic emission spectrometric determination of acid-soluble metal elements chromium,manganese, zinc and copper in talcum powder%电感耦合等离子体原子发射光谱法测定滑石粉中酸溶金属元素铬锰锌铜

    Institute of Scientific and Technical Information of China (English)

    胡晓静; 曾泽; 王长文; 仇薪越; 牟明仁; 富瑶; 沈桂玲; 刘向宽

    2011-01-01

    After digestion by aqua regia with microwave and selection of corresponding spectral lines at 267. 7, 257. 6, 213. 8 and 324. 7 nm as analytical lines, the acid-dissoluble metal elements including chromium, manganese, zinc and copper in talcum powder were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) under optimized conditions with radio frequency power of 1 250 W, auxiliary air flow rate of 0. 60 L/min and atomizer pressure of 26 psi. When the concentration of each testing element was 2. 0 μg/mL, the interferences caused by 20. 0 μg/mL of I-ron, magnesium, calcium, aluminum, zinc, nickel and copper were all less than 5 %. Since the contents of these elements in talcum powder were less than 1 %, their influence on the determination could be ignored. The detection limits of chromium, manganese, zinc and copper were 0. 004 8, 0. 003 8, 0. 001 and 0. 002 6 μg/mL, respectively. This proposed method was applied in actual samples, and the determination results were consistent with those obtained by inductively coupled plasma mass spectrometry (ICP-MS) with relative standard deviations (RSD, n = 8) of 1.1%-4. 2% and recoveries of 93 %-107 %.%以王水作溶剂,微波消解法消解样品,选择267.7、257.6、213.8和324.7 nm波长的光谱线分别作为铬、锰、锌和铜的分析线,在发射功率为1 250 W、辅助气流量为0.60 L/min、雾化器压力为26 psi的优化条件下以电感耦合等离子体原子发射光谱法(ICP-AES)测定了滑石粉中酸溶金属元素铬、锰、锌、铜含量.样品中的基体组分硅酸镁在王水中的溶解量很少,对测定没有影响.当测定待测元素浓度均为2.0μg/mL的溶液时,20.0 μg/mL的铁、镁、钙、铝、锌、镍、铜对待测元素的干扰均小于5%.由于滑石粉中这些元素含量小于1%,因此它们对测定的影响可以忽略.铬、锰、锌、铜的检出限分别为0.004 8、0.003 8、0.001、0.002 6μg/mL.滑石粉样品分析

  8. 电感耦合等离子体发射光谱法测定镍矿石中镍铝磷镁钙%Determination of Ni, AI, P, Mg and Ca in Nickel Ores by Inductively Coupled Plasma-Atomic Emission Spectrometry

    Institute of Scientific and Technical Information of China (English)

    张超; 李享

    2011-01-01

    The simultaneous determination of Ni, Al, P, Mg, and Ca in nickel ores by inductively coupled plasma atomic emission spectrometry (ICP-AES) has been developed and is described in this paper. The sample was dissolved in nitric acid with hydrofluoric acid as flux. Perchloric acid was added and heated in order to remove hydrofluoric acid. After dissolving the salts with hydrochloric, Ni, Al, P, Mg and Ca were determined by ICP-AES. The selected spectral lines forNi, Al, P, Mg and Ca were 221. 6 nm, 396.1 nm, 178. 2 nm, 285. 2 nm and 393. 3 nm, respectively. The matrix effect was corrected by adding the same amount of Fe as the measured sample into the standard curve. The recoveries were 98. 00% -100.50%. The precisions of Ni, Al, P, Mg and Ca were all less than 1 % and the detection limits were 0. 0054 μg/mL, 0. 0028 μg/mL, 0. 0060 μg/mL, 0. 0030 μg/mL and 0. 0013 μg/mL, respectively. Compared with other methods, this method increased sensitivity and decreased the detection limit. It was applied to the determination of nickel ores from Indonesia, and the measured results were consistent with the standard values and RSD was below 1 % ( n = 6 ).%样品用硝酸溶解,氢氟酸助溶,高氯酸冒烟除去氢氟酸,盐酸溶解盐类后,在选定的测量条件下用电感耦合等离子体发射光谱法( ICP - AES)测定镍矿中镍、铝、磷、镁、钙.选择Ni 221.6 nm、Al 396.1nm、P 178.2 nm、Mg 285.2 nm、Ca 393.3 nm分别作为镍、铝、磷、镁、钙的分析线;通过在标准曲线中加入与待测样品等量的铁,消除基体干扰的影响.方法回收率为98.0% ~ 100.5%,镍、铝、磷、镁、钙的精密度均小于1%,检出限分别为0.0054、0.0028、0.0060、0.0030、0.0013 μg/mL.与同类ICP - AES方法比较,本法灵敏度提高,检出限降低.方法用于测定印度尼西亚的两批次镍矿石样品,结果与化学法的测定值基本一致,相对标准偏差小于1%(n=6).

  9. Determination of Cr, V and P in Ilmenite by Inductively Coupled Plasma-Atomic Emission Spectrometry with Sodium Peroxide Fusion%过氧化钠碱熔-电感耦合等离子体发射光谱法测定钛铁矿中铬磷钒

    Institute of Scientific and Technical Information of China (English)

    王卿; 赵伟; 张会堂; 周长祥; 回寒星

    2012-01-01

    An analytical method for the determination of trace elements of Cr, P and V in ilmenite with sodium peroxide by Inductively Coupled Plasma-Atomic Emission Spectrometry ( ICP-AES ) is proposed. The sample was digested by sodium peroxide fusion following which, the clear top solution was acidized to measure Cr, P and V by ICP-AES. The optimum instrumental conditions and selection of spectral lines for the elemental analysis were studied. The large dilution of 1000 and calibration standard solution by adding sodium as the matrix were conducted to eliminate the matrix effect. 2 mL HC1 was loaded to acidize the sample solution in order to avoid eroding the machines sampling system by the strong basicity of the solution by sodium peroxide fusion. The detection limit of this method was 4.46 -23.55 fig/g. According to the validation by national standard materials, the accuracy of the method (relative error) was less than 10% , and precision (RSD, n = 12) was 0.68% to 9. 90%. Compared with the spectrophotometer method for single element determination, this method showed many advantages, such as a low detection limit, high sensitivity, a wide measuring range, convenient operation, and was suitable for batch samples.%样品经过氧化钠碱熔,溶解后的上层清液直接酸化,用电感耦合等离子体发射光谱测定钛铁矿中铬、磷、钒的含量.确定了钛铁矿石中Cr、P、V的分析谱线、光谱级次;为了消除钠盐基体的影响,确定稀释因子为1000,标准曲线基体与样品基体保持一致;为避免过氧化钠熔矿后溶液碱性较大对选样系统造成腐蚀,加入2.00 mL盐酸对溶液进行酸化.方法检出限为4.46 ~23.55μg/g,采用国家一级标准物质进行验证,方法准确度小于10%,精密度为0.68%~9.90%.本法与分光光度法单一元素测定相比较,具有测量范围宽、结果准确、操作简便、省时省力、适合大批量样品测定等突出的优点.

  10. 碱熔-电感耦合等离子体发射光谱法测定大气颗粒物样品中无机元素%Quantification of Inorganic Elements in Aerosol Samples by Inductively Coupled Plasma-Atomic Emission Spectrometry with Alkali Melting

    Institute of Scientific and Technical Information of China (English)

    付爱瑞; 陈庆芝; 罗治定; 姜云军; 金倩; 王芸

    2011-01-01

    大气颗粒物(TSP和PM10)中Si、Al、Ca、Mg、K、Fe、Na等元素含量较高,是颗粒物源分析的指示性元素.目前分析大气颗粒物样品中无机元素的方法有中子活化分析法、X射线荧光光谱法、微波消解(或高压釜消解)电感耦合等离子体发射光谱法和电感耦合等离子体质谱法.本文建立了碱熔-电感耦合等离子体发射光谱法测定大气颗粒物样品中Si、Al、Ca、Mg、Fe、Ti、Ba、Sr、Zr等无机元素的分析方法,样品于镍坩埚中530~550℃灰化60 min后用NaOH融熔,水提取,再用2 mL 50%的HCl酸化,钠基体匹配消除干扰,解决了大气颗粒物滤膜样品中Si易产生的溶解不完全等问题,提高了Ti、Ba、Sr、Zr等主、次量元素测定的精密度和准确度.讨论了坩埚和熔剂的选择、灰化温度、灰化时间、酸度、干扰等影响因素.在选定条件下,测定结果相对误差(RE)﹤4%,相对标准偏差(RSD,n=12)﹤5%,检出限为0.0047~1.2 ng/g.方法所需设备简单,分析成本低,快速简便,精密度好,准确度高,适宜批量样品的测定.%In atmospheric particles ( TSP and PM10 ), the high contents of some inorganic elements including Si, Al, Ca, Mg, K, Fe and Na are the proxy elements for the particles source analysis. At present, there are several methods to analyze inorganic elements for atmospheric particles such as neutron activation analysis, X-ray Fluorescence Spectrometry ( XRF ), Inductively Coupled Plasma-Atomic Emission Spectrometry ( ICP-AES ) and Inductively Coupled Plasma-Mass Spectrometry ( ICP-MS ) after dissolving by microwave ( or high-pressured cauldron ). The established method for determining Si, Al, Ca, Mg, Fe, Ti, Sr, Ba and Zr in aerosols by ICP-AES with alkali melting solved the problems of incomplete dissolving for Si caught in an atmospheric particles filter diaphragm, and improved the precision and accuracy of the determinations of major and trace elements such as Ti, Ba, Sr, Zr. In

  11. Absorption/emission spectroscopy and applications using shock tubes

    Science.gov (United States)

    Sulzmann, K. G. P.

    1988-09-01

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

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

    Science.gov (United States)

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

    2016-08-22

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

  13. Hard X-ray emission spectroscopy with pink beam

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-06-01

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

  14. Photon emission spectroscopy of ion-atom collisions

    Energy Technology Data Exchange (ETDEWEB)

    Nystroem, B.

    1995-10-01

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

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

    Science.gov (United States)

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

    2017-01-01

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

  16. Emission Line Imaging and Spectroscopy of Distant Galaxies

    DEFF Research Database (Denmark)

    Zabl, Johannes Florian

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2011-01-01

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

  18. Determination of Aluminium Content in Aluminium Hydroxide Formulation by FT-NIR Transmittance Spectroscopy

    DEFF Research Database (Denmark)

    Lai, Xuxin; Zheng, Yiwu; Søndergaard, Ib

    2007-01-01

    A method for determining the aluminium content of an aluminium hydroxide suspension using near infrared (NIR) transmittance spectroscopy has been developed. Inductively coupled plasma-atomic emission spectroscopy (ICP-AES) was used as reference method. The factors influencing the NIR analysis......-AES and NIR transmittance spectroscopy exhibit comparable precision and accuracy. The NIR method provides several advantages: no complicated sample preparation; easy to operate; fast and non-destructive. In conclusion, NIR transmittance spectroscopy can be an alternative analytical method for determining...

  19. Determination of cobalt, nickel, iron, niobium, tantalum, vanadium and chrome in tungsten-based hard alloy by microwave digestion-inductively coupled plasma atomic emission spectrometry%微波消解-电感耦合等离子体原子发射光谱法测定钨基硬质合金中钴镍铁铌钽钒铬

    Institute of Scientific and Technical Information of China (English)

    成勇; 彭慧仙; 袁金红; 胡金荣

    2013-01-01

    以硝酸和磷酸(V(HNO3)∶V(H3PO4)=5∶1)作为消解试剂,采取高压密闭微波加热方法对钨钴或钨镍类钨基硬质合金样品进行消解,消解液用水定容后直接以电感耦合等离子体原子发射光谱法(ICP-AES)测定0.005%~10% Co、Ni和0.005%~1% Fe、Nb、Ta、V、Cr、Mo的含量.考察了消解试剂中的硝酸和磷酸量对试样消解的影响以及微波控制参数等最佳消解条件,建立了微波消解-无机试剂络合基体钨的样品消解方法,从而避免了因钨酸沉淀析出而导致部分待测元素损失和使用有机络合剂对光谱测定的干扰影响.实验结果表明:采用以5 min升温至130℃并保持5 min,再以5 min升温至190℃并保持15 min的消解程序,样品的消解效果较好.试验通过优选元素分析谱线,基体匹配和同步背景校正法消除了高钨基体的影响和光谱干扰,确保了方法的可靠性.背景等效浓度值从5 μg/L (Nb)至18 μg/L(Fc),元素检出限从4 μg/L (Nb)至13 μg/L (Fe).方法用于钨基硬质合金样品中上述合金或杂质元素的测定,RSD<3%,加标回收率在97%~104%之间,测定结果与国家标准方法检测结果对照一致.%The tungsten-based hard alloy samples (such as tungsten-cobalt and tungsten-nickel) were digested by high pressure closed microwave heating method using nitric acid-phosphoric acid (V(HNO3) : V(H3PO4)=5 :1) as digestion reagent. After dilution with water, the content of Co, Ni (0.005%-10%), Fe, Nb, Ta, V, Cr and Mo (0. 005%-l%) in digestion solution was directly determined by microwave digestion-inductively coupled plasma atomic emission spectrometry (ICP-AES). The effect of nitric acid and phosphoric acid concentration on sample digestion was investigated. The optimal digestion conditions such as microwave control parameters were studied. The sample digestion method by microwave digestion was established. The matrix tungsten was complexed with inorganic reagents

  20. 超声辅助萃取-电感耦合等离子体原子发射光谱仪联用同时测定水样中多种金属离子%Simultaneous determination of metal ions in water samples by ultrasound-assisted extraction coupled with inductively coupled plasma atomic emission spectrometry

    Institute of Scientific and Technical Information of China (English)

    宋杨; 孟楚桥; 朱田; 高庆历; 聂红霞; 谭彩云; 祁艳霞; 赵前程

    2015-01-01

    目的:优化超声辅助乳化萃取结合电感耦合等离子体(inductively coupled plasma, ICP)原子发射法,同时测定水样中镉、钴、镍、锌4种金属离子。方法采用吡咯烷二硫代氨基甲酸铵(APDC)溶液作为螯合剂,超声条件下采用二氯甲烷对重金属螯合物进行萃取。优化了缓冲液的 pH 值,测定了不同加标浓度下方法的回收率。并对自来水、矿泉水、海水等水样进行了测定。结果该方法对Cd、Co、Ni、Zn 4种金属离子在200μg/L加标条件下绝对回收率为27.0%~91.0%,检出限为Cd为0.81μg/L, Co为1.03μg/L, Ni为1.28μg/L, Zn为0.14μg/L。检测实际自来水样,镉、钴、镍、锌4种金属离子相对回收率分别为96.4%、77.4%、120.2%、85.6%,所测自来水中镉、钴、镍、锌4种金属含量分别为1μg/L、0μg/L、2μg/L和146μg/L,均符合国标要求。对矿泉水中镉、钴、镍的相对回收率分别为77.8%,89.9%和74.2%。矿泉水中没有检测到镉、钴两种金属离子,镍含量为1μg/L。结论该方法适合于自来水和矿泉水中部分金属离子的测定,不适合于对海水中金属离子的测定。%Objective To optimize the ultrasonic-assisted emulsification extraction combined with inductively coupled plasma atomic emission spectrometry (ICP-OES) in order to determinate the concentration of cadmium, cobalt, nickel and zinc in water simultaneously.MethodsAmmonium pyrrolidinedithio carbamate (APDC) was used as a chelating agent, and dichloromethane was used as the extraction reagent of the heavy metal chelating ultrasonic extraction. The pH of the buffer was optimized, and the recovery of every metal ion was measured at different spiked concentration. And the concentration of metal ions in tap water, mineral water and sea water were determined. Results The absolute recovery of Cd, Co, Ni, Zn 4 kinds of metal ions in 200 μg/L spiked conditions were between 27.0%~91.0%, and the detection limits of method were Cd 0

  1. Trapping effect on a small molecular drug with vascular-disrupting agent CA4P in rodent H22 hepatic tumor model: in vivo magnetic resonance imaging and postmortem inductively coupled plasma atomic emission spectroscopy.

    Science.gov (United States)

    Gao, Meng; Yao, Nan; Huang, Dejian; Jiang, Cuihua; Feng, Yuanbo; Li, Yue; Lou, Bin; Peng, Fei; Sun, Ziping; Ni, Yicheng; Zhang, Jian

    2015-06-01

    The aim of the present study is to verify the trapping effect of combretastatin A-4-phosphate (CA4P) on small molecular drugs in rodent tumors. Mice with H22 hepatocarcinoma were randomized into groups A and B. Magnetic resonance imaging (MRI) of T1WI, T2WI, and DWI was performed as baseline. Mice in group A were injected with Gd-DTPA and PBS. Mice in group B were injected with Gd-DTPA and CA4P. All mice undergo CE-T1WI at 0 h, 3 h, 6 h, 12 h, and 24 h. Enhancing efficacy of the two groups on CE-T1WI was compared with the signal-to-noise ratio (SNR) calculated. Concentrations of gadolinium measured by ICP-AES in the tumor were compared between groups. On the early CE-T1WI, tumors were equally enhanced in both groups. On the delayed CE-T1WI, the enhancing effect of group A was weaker than that of group B. The SNR and the concentration of gadolinium within the tumor of group A were lower than that of group B at 6 h, 12 h, and 24 h after administration. This study indicates that CA4P could improve the retention of Gd-DTPA in the tumor and MRI allowed dynamically monitoring trapping effects of CA4P on local retention of Gd-DTPA as a small molecular drug.

  2. Solid phase extraction of Cd, Cu, and Ni from leafy vegetables and plant leaves using amberlite XAD-2 functionalized with 2-hydroxy-acetophenone-thiosemicarbazone (HAPTSC) and determination by inductively coupled plasma atomic emission spectroscopy.

    Science.gov (United States)

    Rao, G Purna Chandra; Seshaiah, Kalluru; Rao, Yerra Koteswara; Wang, M C

    2006-04-19

    A method for solid phase extraction of trace metals, namely, Cd, Cu, and Ni, using Amberlite XAD-2 functionalized with a new chelating ligand, 2-hydroxy-acetophenone-3-thiosemicarbazone (Amberlite XAD-2-HAPTSC), has been developed. The optimum experimental conditions for the quantitative sorption of three metals, pH, effect of flow rate, concentration of eluent, sorption capacity, kinetics of sorption, and the effect of diverse ions on the sorption of analytes have been investigated. The chelating resin could be reused for more than 20 cycles of sorption-desorption without any significant change (<1.5%). The accuracy of the proposed procedure was evaluated by standard reference materials. The proposed method was applied for the determination of trace metal ions in leafy vegetable samples collected from different sources and medicinal plant leaves.

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

    Science.gov (United States)

    2012-02-01

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

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

    Science.gov (United States)

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

    2015-04-01

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

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

    Science.gov (United States)

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

    2017-06-15

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

  6. Avalanche photodiode based detector for beam emission spectroscopy.

    Science.gov (United States)

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

    2010-10-01

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2006-01-01

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

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

    Science.gov (United States)

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

    2015-09-01

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

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

    NARCIS (Netherlands)

    Groot, F.M.F. de

    2000-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-04-08

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

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

    Science.gov (United States)

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

    2016-08-01

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

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

    Science.gov (United States)

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

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

    Science.gov (United States)

    Guthrie, Daniel K.

    1998-09-01

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

  14. Absorption and emission spectroscopy in natural and synthetic corundum

    Science.gov (United States)

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

    2009-04-01

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

  15. Gd-DTPA T1 relaxivity in brain tissue obtained by convection-enhanced delivery, magnetic resonance imaging and emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Haar, Peter J [Department of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA (United States); Broaddus, William C; Chen Zhijian; Gillies, George T [Department of Neurosurgery, Virginia Commonwealth University, Richmond, VA (United States); Fatouros, Panos P; Corwin, Frank D, E-mail: wbroaddus@mcvh-vcu.ed [Department of Radiology, Virginia Commonwealth University, Richmond, VA (United States)

    2010-06-21

    A common approach to quantify gadolinium (Gd) contrast agents involves measuring the post-contrast change in T1 rate and then using the constant T1 relaxivity R to determine the contrast agent concentration. Because this method is fast and non-invasive, it could be potentially valuable in many areas of brain research. However, to accurately measure contrast agent concentrations in the brain, the T1 relaxivity R of the specific agent must be accurately known. Furthermore, the macromolecular content and compartmentalization of the brain extracellular space (ECS) are expected to significantly alter R from values measured in aqueous solutions. In this study, the T1 relaxivity R of gadolinium-diethylene-triamine penta-acetic acid (Gd-DTPA) was measured following direct interstitial infusions of three different contrast agent concentrations to the parenchyma of rat brains. Changes in magnetic resonance (MR) T1 values were compared to brain slice concentrations determined with inductively coupled plasma atomic emission spectroscopy (ICP-AES) to determine R in 15 rats. Additionally, samples of cerebrospinal fluid, blood and urine were analyzed to evaluate possible Gd-DTPA clearance from the brain. The T1 relaxivity R of Gd-DTPA in the brain ECS was measured to be 5.35 (mM s){sup -1} in a 2.4 T field. This value is considerably higher than estimations used in studies by other groups. Measurements of brain Gd-DTPA tissue concentrations using MRI and ICP-AES demonstrated a high degree of coincidence. Clearance of Gd-DTPA was minimal at the time point immediately after infusion. These results suggest that the environment of the brain does in fact significantly affect Gd T1 relaxivity, and that MRI can accurately measure contrast agent concentrations when this relaxivity is well characterized.

  16. Analysis of accumulation, extractability, and metabolization of five different phenylarsenic compounds in plants by ion chromatography with mass spectrometric detection and by atomic emission spectroscopy.

    Science.gov (United States)

    Schmidt, Anne-Christine; Kutschera, Kristin; Mattusch, Jürgen; Otto, Matthias

    2008-12-01

    Phenylated arsenic compounds occur as highly toxic contaminants in former military areas where they were formed as degradation products of chemical warfare agents. Some phenylarsenic compounds such as roxarsone and aminophenylarsonic acids were applied as food additive and veterinary drugs in stock-breeding and therefore pose an environmental risk in agricultural used sites. Very few data exist in the literature concerning uptake and effects of phenylarsenic compounds in plants growing on contaminated soils. In this study, the accumulation, extractability, and metabolization of five different phenylarsenic compounds, phenylarsonic acid, p- and o-aminophenylarsonic acid, phenylarsine oxide, and 3-nitro-4-hydroxyphenylarsonic acid called roxarsone, by the terrestrial plant Tropaeolum majus were investigated. Ion chromatography coupled to inductively coupled plasma mass spectrometry was used to differentiate these arsenic compounds, and inductively coupled plasma atomic emission spectroscopy was used for total arsenic quantification. All compounds considered were taken up by the roots and transferred to stalks, leaves, and flowers. The strongest accumulation was observed for unsubstituted phenylarsonic acid followed by its trivalent analogue phenylarsine oxide that was mostly oxidized in soil whereas the amino- or nitro- and hydroxy-substituted phenylarsonic acids were accumulated to a smaller degree. The highest extraction yield of 90% for ground leaf material was achieved by 0.1M phosphate buffer, pH 7.7, in a two-step extraction with a total extraction time of 24h. The extraction of higher amounts of arsenic (50-70% of total arsenic present in leaves depending on arsenic species application) from non-ground intact leaves with deionized water in comparison with the buffer (20-40% of total arsenic) is ascribed to osmotic effects. The arsenic species analysis revealed a cleavage of the amino groups from the phenyl ring for plants treated with aminophenylarsonic acids

  17. 微波消解-耐氢氟酸系统进样电感耦合等离子体发射光谱法测定锰矿中铝磷镁铁锌镍%Determination of aluminum, phosphorus, magnesium, iron, zinc and nickel in manganese ore by inductively coupled plasma atomic emission spectrometry with hydrofluoric add resistant sampling system after microwave digestion

    Institute of Scientific and Technical Information of China (English)

    邓全道; 许光; 林冠春; 刘建发; 刘灵芝

    2011-01-01

    采用混合酸作溶剂微波消解试样,样液定客后,直接用耐氢氟酸进样系统(Duo HF KIT)进样,电感耦合等离子体发射光谱法(ICP-AES)测定锰矿石试液中的铝、磷、镁、铁、锌、镍,避免因为引入硼酸掩蔽氟离子而带来的基体干扰,缩短了检测时间.测定时选择波长为369.152 nm{85}、186.942 nm{481}、280.270 nm{120}、240.488 nm{140}、213.856 nm{457}和341.476 nm{99}光谱线分别作为Al、P、Mg、Fe、Zn、Ni分析线,采用基体匹配方法来消除锰的基体效应.本法已测定国家锰矿标准物质中铝、磷、镁、铁、锌、镍,并与国标方法测定结果相比对,分析结果与认定值及国标方法的测定值相符,且重复性好.各元素的加标回收率为94%~107%,测定结果的相对标准偏差(RSD,n=12)小于1.1%.%The samples were dissolved by microwave digestion using mixed acid as solvent. After dilution, the aluminum, phosphorus, magnesium, iron, zinc and nickel in manganese ore were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) using hydrofluoric acid resistant sampling system (Duo HF KIT). The matrix effect of boric acid introduced for masking fluorine ion was prevented , and the detection time was shortened. The spectral lines for Al, P, Mg, Fe, Zn and Ni were 369. 152 nm{ 85 } , 186. 942 nm{ 481 } , 280. 270 nm{120} , 240. 488 nm {140} , 213. 856 nm {457} and 341. 476 nm {99}, respectively. The matrix effect of manganese was eliminated by matrix matching method. The proposed method had been applied to the determination of aluminum, phosphorus, magnesium, iron, zinc and nickel in certified reference materials of manganese ore. The determination results were compared with those obtained by national standard method. It was found that the analytical results were consistent with the certified values and those obtained by national standard method. Moreover, the repeatability was good. The recoveries of elements were 94%-107

  18. Multiple stimulated emission fluorescence photoacoustic sensing and spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-07-04

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

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

    Science.gov (United States)

    Poole, Zsolt L; Ohodnicki, Paul R

    2016-04-01

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

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

    Science.gov (United States)

    Waldmann, Ingo

    2010-01-01

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

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

    OpenAIRE

    de Groot, F. M. F.

    2001-01-01

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

  2. Non-coincident multi-wavelength emission absorption spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Baumann, L.E.

    1995-02-01

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

  3. Detailed computation of hot-plasma atomic spectra

    CERN Document Server

    Pain, Jean-Christophe; Blenski, Thomas

    2015-01-01

    We present recent evolutions of the detailed opacity code SCO-RCG which combines statistical modelings of levels and lines with fine-structure calculations. The code now includes the Partially-Resolved-Transition-Array model, which allows one to replace a complex transition array by a small-scale detailed calculation preserving energy and variance of the genuine transition array and yielding improved high-order moments. An approximate method for studying the impact of strong magnetic field on opacity and emissivity was also recently implemented. The Zeeman line profile is modeled by fourth-order Gram-Charlier expansion series, which is a Gaussian multiplied by a linear combination of Hermite polynomials. Electron collisional line broadening is often modeled by a Lorentzian function and one has to calculate the convolution of a Lorentzian with Gram-Charlier distribution for a huge number of spectral lines. Since the numerical cost of the direct convolution would be prohibitive, we propose, in order to obtain t...

  4. Detection of Bioaerosols using Single Particle Thermal Emission Spectroscopy

    Science.gov (United States)

    2013-03-01

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

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

    OpenAIRE

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

    2015-01-01

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

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

    Science.gov (United States)

    2013-03-01

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

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

    Science.gov (United States)

    Buchele, D. R.

    1994-01-01

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

  8. 40 CFR Table 4 to Subpart Uuu of... - Requirements for Performance Tests for Metal HAP Emissions From Catalytic Cracking Units Not...

    Science.gov (United States)

    2010-07-01

    ... Plasma-Atomic Emission Spectrometry, EPA Method 6020, Inductively Coupled Plasma-Mass Spectrometry, EPA Method 7520, Nickel Atomic Absorption, Direct Aspiration, and EPA Method 7521, Nickel Atomic...

  9. Ground-based NIR emission spectroscopy of HD189733b

    CERN Document Server

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

    2011-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2008-01-01

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

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

    Science.gov (United States)

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

    1998-01-01

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

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

    Science.gov (United States)

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

  13. 2p3d Resonant X-ray emission spectroscopy of cobalt compounds

    NARCIS (Netherlands)

    van Schooneveld, M.M.

    2013-01-01

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

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

    CERN Document Server

    Zhang, Heshou; Richter, Philipp

    2016-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1981-01-01

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

  16. 溴-甲醇提取-电感耦合等离子体原子发射光谱法测定红土镍矿还原产物中金属镍%Determination of metallic nickel in reducing products of nickel laterite ore by inductively coupled plasma atomic emission spectrometry after bromine-methanol extraction

    Institute of Scientific and Technical Information of China (English)

    李博; 王华; 魏永刚

    2011-01-01

    The metallic nickel in reducing products of nickel laterite ore was extracted by bromine-methanol. After filtering and separating the insoluble residue, the filtrate was evaporated to dryness. The residual was then dissolved in hydrochloric acid. The 231. 604 nm was selected as analytical spectral line of nickel. The content of nickel in solution was determined by inductively coupled plasma a-tomic emission spectrometry under optimal instrumental conditions. Hence, the content of metallic nickel could be calculated. The influence of sample size, extraction time, bromine concentration, dosage of bromine-methanol and interference elements on determination results was studied. Moreover, the sample analysis and recovery test were performed. The results showed that, when the sample size was smaller than 0.1 mm, and the metallic nickel was extracted with 100 mL of 5 % (V/V) bromine-methanol for 90 min, the determination results were best. Under this condition, some other active metal elements such as magnesium, aluminum and iron could be also extracted. Since their spectral lines would be overlapped with that of nickel, the determination of nickel would be affected. However, the interference could be eliminated by background correction method. The proposed method was applied to the determination of metallic nickel in reducing products of nickel laterite ore. The relative standard deviations (RSD) of determination results were in the range of 0. 96 % -5. 9 %. The recoveries of standard addition were 97. 8% -103. 8%.%采用溴-甲醇提取红土镍矿还原产物中金属镍,过滤分离不溶残渣,滤液蒸干后用盐酸溶解,选择231.604nm作为镍的分析谱线,在最佳的仪器条件下用电感耦合等离子体原子发射光谱法测定溶液中镍的含量,然后通过计算得出金属镍的含量.研究了样品粒度、提取时间、溴浓度、溴-甲醇用量、干扰元素对测定结果的影响,并进行了样品分析和回收率实验.结

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

    Science.gov (United States)

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

    1985-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-10-15

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

  19. Solving a Mock Arsenic-Poisoning Case Using Atomic Spectroscopy

    Science.gov (United States)

    Tarr, Matthew A.

    2001-01-01

    A new upper-level undergraduate atomic spectroscopy laboratory procedure has been developed that presents a realistic problem to students and asks them to assist in solving it. Students are given arsenic-laced soda samples from a mock crime scene. From these samples, they are to gather evidence to help prosecute a murder suspect. The samples are analyzed by inductively coupled plasma atomic emission spectroscopy or by atomic absorbance spectroscopy to determine the content of specific metal impurities. By statistical comparison of the samples' composition, the students determine if the soda samples can be linked to arsenic found in the suspect's home. As much as possible, the procedures and interpretations are developed by the students. Particular emphasis is placed on evaluating the limitations and capabilities of the analytical method with respect to the demands of the problem.

  20. Identification of microcrystalline rocks using thermal emission spectroscopy

    Science.gov (United States)

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

    2015-12-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1997-08-01

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

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

    Science.gov (United States)

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

    2009-11-15

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

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

    Science.gov (United States)

    Ma, Qianli; Dagdigian, Paul J

    2011-07-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2001-03-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1995-12-01

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

  6. [Analytical figures of merit of Hildebrand grid and ultrasonic nebulizations in inductively coupled plasma atomic emission].

    Science.gov (United States)

    Tian, Mei; Han, Xiao-yuan; Zhuo, Shang-jun; Zhang, Rui-rong

    2012-05-01

    Hildebrand grid nebulizer is a kind of improved Babington nebulizer, which can nebulize solutions with high total dissolved solids. And the ultrasonic nebulizer (USN) possesses advantage of high nebulization efficiency and fine droplets. In the present paper, the detection limits, matrix effects, ICP robustness and memory effects of Hildebrand grid and ultrasonic nebulizers for ICP-AES were studied. The results show that the detection limits using USN are improved by a factor of 6-23 in comparison to Hildebrand grid nebulizer for Cu, Pb, Zn, Cr, Cd and Ni. With the USN the matrix effects were heavier, and the degree of intensity enhancement and lowering depends on the element line, the composition and concentrations of matrices. Moreover, matrix effects induced by Ca and Mg are more significant than those caused by Na and Mg, and intensities of ionic lines are affected more easily than those of atomic lines. At the same time, with the USN ICP has less robustness. In addition, memory effect of the USN is also heavier than that of Hildebrand grid nebulizer.

  7. Infrared laser ablation study of pressed soil pellets with inductively coupled plasma atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Mikolas, J.; Musil, P.; Stuchlikova, V.; Novotny, K.; Otruba, V.; Kanicky, V. [Laboratory of Atomic Spectrochemistry, Faculty of Science, Masaryk University Brno, Kotlarska 2, 61137 Brno (Czech Republic)

    2002-09-01

    Potential of infrared laser ablation (LA) coupled with ICP-AES as a technique suitable for the determination of trace elements (Zn, Cu, Ni, Cr, and V) in agricultural soils was studied. Operating parameters such as laser beam energy, laser beam focusing with respect to the sample surface, and velocity of the sample translation in the plane perpendicular to the laser beam were optimized. Soil samples were mixed with powdered Ag as a binder, and an internal standard (GeO{sub 2}), and pressed into pellets. Calibration samples were prepared by adding known amounts of oxides of elements of interest into soils of known elemental composition and then processed in the same way as the analyzed samples. Calibration curves were found to be linear at least up to several hundreds of mg kg{sup -1} for the elements of interest. The elemental contents obtained by using LA-ICP-AES were compared with those obtained by analysis using wet chemistry followed by ICP-AES with pneumatic nebulization (PN). The results were in good agreement. Accuracy was also tested using certified reference soils with a bias not exceeding 10% relative. (orig.)

  8. Determination of trace elements in heroin by inductively coupled plasma atomic emission spectrometry using ultrasonic nebulization

    Science.gov (United States)

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-01-01

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

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

    Science.gov (United States)

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

    2016-07-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2010-05-15

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

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

    Science.gov (United States)

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

    2016-05-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-11-15

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

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

    Science.gov (United States)

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

    2016-09-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Mariotti, D

    2002-04-01

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

  16. Quantitative analysis of gallstones using laser-induced breakdown spectroscopy.

    Science.gov (United States)

    Singh, Vivek K; Singh, Vinita; Rai, Awadhesh K; Thakur, Surya N; Rai, Pradeep K; Singh, Jagdish P

    2008-11-01

    The utility of laser-induced breakdown spectroscopy (LIBS) for categorizing different types of gallbladder stone has been demonstrated by analyzing their major and minor constituents. LIBS spectra of three types of gallstone have been recorded in the 200-900 nm spectral region. Calcium is found to be the major element in all types of gallbladder stone. The spectrophotometric method has been used to classify the stones. A calibration-free LIBS method has been used for the quantitative analysis of metal elements, and the results have been compared with those obtained from inductively coupled plasma atomic emission spectroscopy (ICP-AES) measurements. The single-shot LIBS spectra from different points on the cross section (in steps of 0.5 mm from one end to the other) of gallstones have also been recorded to study the variation of constituents from the center to the surface. The presence of different metal elements and their possible role in gallstone formation is discussed.

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

    Science.gov (United States)

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

    2016-07-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-07-01

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

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

    Science.gov (United States)

    McLaren, Ian A.; Wrobel, Jacek D.

    1997-01-01

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

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

    Science.gov (United States)

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

    2017-10-01

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

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

    Science.gov (United States)

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

    2016-12-01

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

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

    Science.gov (United States)

    Blacklock, E C; Sadler, P A

    1981-06-02

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

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

    Science.gov (United States)

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

    2016-06-01

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

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

    Science.gov (United States)

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

    2011-03-01

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

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

    Science.gov (United States)

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

    2015-07-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2005-09-15

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1997-12-31

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

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

    OpenAIRE

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

    2017-01-01

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

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

    Science.gov (United States)

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

    2005-09-01

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

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

    CERN Document Server

    Rajasekaran, Priyadarshini; Awakowicz, Peter

    2012-01-01

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

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

    CERN Document Server

    Lamberti, Carlo

    2016-01-01

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

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

    CERN Document Server

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

    2016-01-01

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

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

    Science.gov (United States)

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

    2015-11-01

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

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

    Science.gov (United States)

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

    2017-03-01

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

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

    CERN Document Server

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

    2012-01-01

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

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

    Science.gov (United States)

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

    2017-02-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-09-15

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

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

    Science.gov (United States)

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

    2017-02-01

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

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

    Science.gov (United States)

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

    2017-01-01

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

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

    Science.gov (United States)

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

    2012-09-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-01-01

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

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

    Science.gov (United States)

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

    2016-03-01

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

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

    Science.gov (United States)

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

    2012-01-01

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

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

    Science.gov (United States)

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

    2016-02-01

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

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

    Directory of Open Access Journals (Sweden)

    Karen J. Brewer

    2010-08-01

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

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

    CSIR Research Space (South Africa)

    Mudau, AE

    2010-09-01

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

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

    Science.gov (United States)

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

    2016-04-01

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2012-01-01

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

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

    Science.gov (United States)

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

    2009-05-01

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

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

    Science.gov (United States)

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

    2013-06-07

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-11-15

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

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

    Science.gov (United States)

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

    2014-12-01

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

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

    Science.gov (United States)

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

    2016-11-01

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

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

    Science.gov (United States)

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

    2010-02-01

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

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

    Science.gov (United States)

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

    2002-10-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2002-10-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2010-11-03

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-07-20

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

  19. Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Hellman, Hal

    1968-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-07-15

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-12-01

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

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

    Science.gov (United States)

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

    2016-09-01

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

  3. Spectroscopy

    CERN Document Server

    Walker, S

    1976-01-01

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

  4. In-situ assessment of metal contamination via portable X-ray fluorescence spectroscopy: Zlatna, Romania.

    Science.gov (United States)

    Weindorf, David C; Paulette, Laura; Man, Titus

    2013-11-01

    Zlatna, Romania is the site of longtime mining/smelting operations which have resulted in widespread metal pollution of the entire area. Previous studies have documented the contamination using traditional methods involving soil sample collection, digestion, and quantification via inductively coupled plasma atomic emission spectroscopy or atomic absorption. However, field portable X-ray fluorescence spectroscopy (PXRF) can accurately quantify contamination in-situ, in seconds. A PXRF spectrometer was used to scan 69 soil samples in Zlatna across multiple land use types. Each site was georeferenced with data inputted into a geographic information system for high resolution spatial interpolations. These models were laid over contemporary aerial imagery to evaluate the extent of pollution on an individual elemental basis. Pb, As, Co, Cu, and Cd exceeded governmental action limits in >50% of the sites scanned. The use of georeferenced PXRF data offers a powerful new tool for in-situ assessment of contaminated soils.

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

    Science.gov (United States)

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

    2016-10-01

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

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

    CERN Document Server

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

    2003-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1997-04-01

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

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

    Science.gov (United States)

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

    2016-06-01

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

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

    Science.gov (United States)

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

    2017-01-01

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

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

    Science.gov (United States)

    van Gastelen, Sanne; Dijkstra, Jan

    2016-09-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-06-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-03-15

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2010-03-15

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

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

    Science.gov (United States)

    Narayanan, V.; Thareja, R. K.

    2004-01-01

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

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

    Science.gov (United States)

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

    2017-06-01

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

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

    Science.gov (United States)

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

    2014-05-14

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

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

    Science.gov (United States)

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

    2012-12-21

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

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

    Science.gov (United States)

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

    2016-05-01

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

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

    Directory of Open Access Journals (Sweden)

    Ricarda Wernitz

    2013-01-01

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

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

    Science.gov (United States)

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

    2017-02-01

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

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

    Science.gov (United States)

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

    2016-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2002-02-01

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

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

    Science.gov (United States)

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

    2017-08-01

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

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

    Science.gov (United States)

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

    2015-09-01

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

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

    Science.gov (United States)

    Rao, Harshvardhan; Gaur, Neeraj; Tipre, Dnyanesh

    2017-04-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2010-07-15

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

  7. 活性炭富集电感耦合等离子体原子发射光谱测定铋系超导粉中痕量铁%Enrichment of Trace Iron with Activated Carbon in Bi-Based Superconductor Powder and Determination by Inductively Coupled Plasma Atomic Emission Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    黄文杰; 李建强; 范慧俐; 范丽新; 包蕊; 张霞; 王杰; 陆青

    2012-01-01

    建立了电感耦合等离子体原子发射光谱(ICP-AES)测定超导粉中痕量铁的新方法.优化了仪器工作参数,对痕量铁测定时的基体干扰及消除干扰的方法进行了系统研究,结果表明:大量存在的基体元素产生一定基体效应,并使重现性变差,且由于铁含量甚微,仪器灵敏度不能满足测定的要求,需采用分离富集方法以提高测定结果的准确度和精密度.以三乙醇胺掩蔽基体元素铋和铜,在适宜的酸度条件下,铁与邻二氮菲生成配合物,以活性炭定量吸附,用1∶1硝酸解吸,并对分离富集条件进行了优化.对模拟标准样品进行测定,分析结果与理论值一致,相对标准偏差为2.4%,方法检出限为0.033μg·g-1.该方法已用于超导前驱粉样品中痕量铁的分析,结果令人满意,并进行了回收实验,回收率为95.6%~98.0%.%A new method for determination of trace iron in superconductor powder by ICP-AES was proposed. The instrument parameters were optimized, and the matrix effects as well as the method of eliminating interferences were also studied systemical-ly. The results showed that matrix interference was serious when the amount of matrix increased, and the repeatability was poor, so it was necessary that separation and preconcentration were used to improve the accuracy and precision. In the experiment , complex was formed with Fe and phenanthroline after the matrix elements Bi and Cu were masked by triethanolamine in an appropriate acidity condition. Then the complex was quantitatively adsorbed by activated carbon, and desorbed by 1 : 1 HNO3.The enrichment conditions were investigated in detail. Under the optimal condition, an artificial sample was analysed, and the result was identical with reference values, with the RSD and detection limit being 2. 42% and 0. 033μg ? G-1, respectively. The method was applied for the determination of trace iron in Bi-based superconductor powder samples with satisfactory results, in which the recoveries experiment was performed with the recovery coefficient falling in the range of 95. 6% to 98. 0%.

  8. Determination of Trace Nickel in Bi-Based Superconductor Powder by Inductively Coupled Plasma Atomic Emission Spectroscopy after Separation with Anion Exchange Resin and Extraction with Methylbenzene%阴离子交换树脂分离甲苯萃取ICP-AES测定铋系超导粉中的痕量镍

    Institute of Scientific and Technical Information of China (English)

    范丽新; 李建强; 范慧俐; 孙建伶; 张霞; 包蕊; 陆青; 王杰

    2011-01-01

    A new method for the determination of trace nickel in superconductor powder by ICP-AES was proposed. The instrument parameters were optimized) and the matrix effects as well as the method of eliminating interferences were also studied sys-temically. The results showed that matrix interference in the superconductor powder was serious when the amount of matrix increased, and the repeatability as well as the accuracy was poor, so it was necessary to used separation and preconcentration to improve the accuracy and precision. In this experiment, Ni-diacetyl dioxime complexes were enriched by toluene extraction in alkaline condition after eliminating the interference of major element Bi and partial Pb, Sr, Ca and Cu by eluting with anion exchange resin, then the Ni-complexes were back extracted by diluted hydrochloric acid. The enrichment conditions were investigated in detail and the recovery rate of Ni was higher than 95%. Under the optimal condition, an artificial sample was analysed, the result showed that the found values were identical with reference values, and the RSD and detection limit were 1. 9% and 0.19 μg ? g-1, respectively. The method has been applied to the determination of trace nickel in Bi-based superconductor powder samples with satisfactory results.%建立了ICP-AES测定超导粉中痕量镍的新方法.优化了仪器工作参数,对超导前驱粉中痕量镍测定时的基体干扰及干扰消除方法进行了系统研究,结果表明:大量存在的基体元素产生严重基体效应,导致测定重现性及准确度变差,实验采用分离富集方法以提高测定结果的准确度和精密度.实验中首先用阴离子交换树脂,除去Bi3+及部分pb2+,Sr2+,Ca2+,Cu2十等基体元素;在碱性条件下再通过甲苯萃取镍与丁二酮肟的络合物、稀盐酸反萃取富集镍;对分离富集条件进行了优化.对模拟标准样品进行测定,分析结果与理论值一致,相对标准偏差为1.9%,方法检出限为0.19 μg·g-1.该方法已用于超导前驱粉样品中痕量镍的分析,结果令人满意.

  9. Spectroscopy

    DEFF Research Database (Denmark)

    Berg, Rolf W.

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

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

    Science.gov (United States)

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

    2012-10-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-10-15

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

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

    Science.gov (United States)

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

    2012-04-01

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

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

    Science.gov (United States)

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

    2011-12-01

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

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

    Science.gov (United States)

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

    2016-09-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2004-07-07

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Augustsson, Andreas [Uppsala Univ. (Sweden)

    2004-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1998-04-01

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

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

    Science.gov (United States)

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

    2017-05-01

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

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

    Science.gov (United States)

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

    2016-10-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-11-15

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

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

    Directory of Open Access Journals (Sweden)

    Mohd Hashim Nurul’Afiqah Hashimah

    2016-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-05-01

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

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

    Science.gov (United States)

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

    1999-04-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Ludwig, Benno

    2009-09-24

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Ludwig, Benno

    2009-09-24

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Digby Macdonald; Brian Marx; Balaji Soundararajan; Morgan Smith

    2005-07-28

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2008-01-15

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-04-01

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

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

    CERN Document Server

    Gika, V; Maltezos, S

    2016-01-01

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

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

    Science.gov (United States)

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

    2016-06-01

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

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

    Data.gov (United States)

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

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

    Science.gov (United States)

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

    2011-09-01

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

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

    Science.gov (United States)

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

    2016-07-01

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

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

    CERN Document Server

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

    2016-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-05-01

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

  16. 40 CFR Appendix C to Part 136 - Inductively Coupled Plasma-Atomic Emission Spectrometric Method for Trace Element Analysis of...

    Science.gov (United States)

    2010-07-01

    ... extremely toxic and may be fatal if swallowed. Wash hands thoroughly after handling.) Typical stock solution....1000 g of manganese metal in the acid mixture 10 mL conc. HCl and 1 mL conc. HNO3, and dilute to 1,000... standard solution I—Manganese, beryllium, cadmium, lead, and zinc. 7.4.2Mixed standard solution...

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

    Science.gov (United States)

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

    2016-01-01

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

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

    Science.gov (United States)

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

    2017-09-01

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

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

    Science.gov (United States)

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

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

    Institute of Scientific and Technical Information of China (English)

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

    2000-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-01-14

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

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

    Science.gov (United States)

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

    2013-07-01

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

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

    Science.gov (United States)

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

    2016-10-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-11-15

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

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

    Science.gov (United States)

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

    2008-06-01

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

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

    CERN Document Server

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

    2015-01-01

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

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

    Science.gov (United States)

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

    2016-08-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2001-12-04

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

  9. Correlation between calcium carbonate content and emission characteristics of incense.

    Science.gov (United States)

    Yang, Chi-Ru; Lin, Ta-Chang; Chang, Feng-Hsiang

    2006-12-01

    In Taiwan and China, calcium carbonate is commonly added as a filler during incense production to lower the cost. This study has found an unexpected benefit for this practice: it reduces particulate emission. Nine types of the popular incense on the local market were chosen for this study. The calcium content in raw material incense was analyzed by inductively coupled plasma atomic emission spectrometry, followed by X-ray diffraction (XRD) spectroscopy. The correlation between the calcium content and emission characteristics of incense was investigated. The calcium content varied from 1.8 to 60 mg/g (incense burned) among those nine different types of incense. Very little calcium (incense. Instead, most calcium was artificially added in the form of CaCO3 during manufacturing. The combustion characteristics, including burning rate, emission factors of particulate, ash, and solid-phase polycyclic aromatic hydrocarbons (S-PAHs), varied significantly among the nine types of incense. Incense containing 2% calcium would emit 30% less S-PAHs, compared with those with little (incense by approximately 50%.

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

    Science.gov (United States)

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

    2013-11-01

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

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

    Science.gov (United States)

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

    2016-04-01

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

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

    Science.gov (United States)

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

    2013-05-01

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

  13. The use of atomic spectroscopy in the pharmaceutical industry for the determination of trace elements in pharmaceuticals.

    Science.gov (United States)

    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.

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

    Science.gov (United States)

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

    2011-12-01

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

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

    Science.gov (United States)

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

    2011-01-01

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

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

    Science.gov (United States)

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

    2017-09-01

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

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

    CERN Document Server

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

    2016-01-01

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

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

    Science.gov (United States)

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

    2017-02-01

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

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

    CERN Multimedia

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

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

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

    Science.gov (United States)

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

    2007-02-01

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

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

    Science.gov (United States)

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

    2017-01-01

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

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

    Science.gov (United States)

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

    2004-10-01

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

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

    CERN Document Server

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

    2015-01-01

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

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

    Science.gov (United States)

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

    2017-01-01

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

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

    Science.gov (United States)

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

    2011-11-01

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

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

    Science.gov (United States)

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

    2015-04-01

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

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

    CERN Document Server

    Coe, J P

    2015-01-01

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

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

    Science.gov (United States)

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

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

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

    OpenAIRE

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

    2016-01-01

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

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

    CERN Document Server

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

    2012-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1999-07-01

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

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

    CERN Document Server

    Ricci, T V; Menezes, R B

    2015-01-01

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

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

    CERN Document Server

    Ricci, T V; Menezes, R B

    2014-01-01

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

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

    CERN Document Server

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

    2011-01-01

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

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

    Science.gov (United States)

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

    2015-03-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2008-05-11

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

  17. Emission Mössbauer spectroscopy study of fluence dependence of paramagnetic relaxation in Mn/Fe implanted ZnO

    Science.gov (United States)

    Masenda, H.; Geburt, S.; Bharuth-Ram, K.; Naidoo, D.; Gunnlaugsson, H. P.; Johnston, K.; Mantovan, R.; Mølholt, T. E.; Ncube, M.; Shayestehaminzadeh, S.; Gislason, H. P.; Langouche, G.; Ólafsson, S.; Ronning, C.

    2016-12-01

    Emission Mössbauer Spectroscopy following the implantation of radioactive precursor isotope 57Mn+ ( T 1/2= 1.5 min) into ZnO single crystals at ISOLDE/CERN shows that a large fraction of 57Fe atoms produced in the 57Mn beta decay is created as paramagnetic Fe3+ with relatively long spin-lattice relaxation times. Here we report on ZnO pre-implanted with 56Fe to fluences of 2×1013, 5×10 13 and 8 × 1013 ions/cm2 in order to investigate the dependence of the paramagnetic relaxation rate of Fe3+ on fluence. The spectra are dominated by magnetic features displaying paramagnetic relaxation effects. The extracted spin-lattice relaxation rates show a slight increase with increasing ion fluence at corresponding temperatures and the area fraction of Fe3+ at room temperature reaches a maximum contribution of 80(3)% in the studied fluence range.

  18. Electronic structure of multiferroic BiFeO3 by resonant soft-x-ray emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Higuchi, Tohru; Higuchi, T.; Liu, Y.-S.; Yao, P.; Glans, P.-A.; Guo, Jinghua; Chang, C.; Wu, Z.; Sakamoto, W.; Itoh, N.; Shimura, T.; Yogo, T.; Hattori, T.

    2008-07-11

    The electronic structure of multiferroic BiFeO{sub 3} has been studied using soft-X-ray emission spectroscopy. The fluorescence spectra exhibit that the valence band is mainly composed of O 2p state hybridized with Fe 3d state. The band gap corresponding to the energy separation between the top of the O 2p valence band and the bottom of the Fe 3d conduction band is 1.3 eV. The soft-X-ray Raman scattering reflects the features due to charge transfer transition from O 2p valence band to Fe 3d conduction band. These findings are similar to the result of electronic structure calculation by density functional theory within the local spin-density approximation that included the effect of Coulomb repulsion between localized d states.

  19. Non-gated laser induced breakdown spectroscopy provides a powerful segmentation tool on concomitant treatment of characteristic and continuum emission.

    Science.gov (United States)

    Myakalwar, Ashwin Kumar; Dingari, Narahara Chari; Dasari, Ramachandra Rao; Barman, Ishan; Gundawar, Manoj Kumar

    2014-01-01

    We demonstrate the application of non-gated laser induced breakdown spectroscopy (LIBS) for characterization and classification of organic materials with similar chemical composition. While use of such a system introduces substantive continuum background in the spectral dataset, we show that appropriate treatment of the continuum and characteristic emission results in accurate discrimination of pharmaceutical formulations of similar stoichiometry. Specifically, our results suggest that near-perfect classification can be obtained by employing suitable multivariate analysis on the acquired spectra, without prior removal of the continuum background. Indeed, we conjecture that pre-processing in the form of background removal may introduce spurious features in the signal. Our findings in this report significantly advance the prior results in time-integrated LIBS application and suggest the possibility of a portable, non-gated LIBS system as a process analytical tool, given its simple instrumentation needs, real-time capability and lack of sample preparation requirements.

  20. Non-gated laser induced breakdown spectroscopy provides a powerful segmentation tool on concomitant treatment of characteristic and continuum emission.

    Directory of Open Access Journals (Sweden)

    Ashwin Kumar Myakalwar

    Full Text Available We demonstrate the application of non-gated laser induced breakdown spectroscopy (LIBS for characterization and classification of organic materials with similar chemical composition. While use of such a system introduces substantive continuum background in the spectral dataset, we show that appropriate treatment of the continuum and characteristic emission results in accurate discrimination of pharmaceutical formulations of similar stoichiometry. Specifically, our results suggest that near-perfect classification can be obtained by employing suitable multivariate analysis on the acquired spectra, without prior removal of the continuum background. Indeed, we conjecture that pre-processing in the form of background removal may introduce spurious features in the signal. Our findings in this report significantly advance the prior results in time-integrated LIBS application and suggest the possibility of a portable, non-gated LIBS system as a process analytical tool, given its simple instrumentation needs, real-time capability and lack of sample preparation requirements.

  1. A study of internal oxidation in carburized steels by glow discharge optical emission spectroscopy and scanning electron microscopy

    CERN Document Server

    An, X; Rainforth, W M; Chen, L

    2003-01-01

    The internal oxidation of Cr-Mn carburizing steel was studied. Internal oxidation was induced using a commercial carburizing process. Sputter erosion coupled with glow discharge optical emission spectroscopy (GDOES) was used to determine the depth profile elemental distribution within the internal oxidation layer (<10 mu m). In addition, scanning electron microscopy (SEM) equipped with energy dispersive spectrometer (EDS) studies were carried out on selected sputter eroded surfaces. Oxide type was identified primarily by transmission electron microscopy (TEM). The carburized surface was found to consist of a continuous oxide layer, followed by a complex internal oxidation layer, where Cr and Mn oxides were found to populate grain boundaries in a globular form in the near surface region. At greater depths (5-10 mu m), Si oxides formed as a grain boundary network. The internal oxides (mainly complex oxides) grew quickly during the initial stages of the carburizing process (2 h, 800 deg. C+3 h, 930 deg. C). G...

  2. Aqueous solutions of uranium(VI) as studied by time-resolved emission spectroscopy: a round-robin test.

    Science.gov (United States)

    Billard, Isabelle; Ansoborlo, Eric; Apperson, Kathleen; Arpigny, Sylvie; Azenha, M Emilia; Birch, David; Bros, Pascal; Burrows, Hugh D; Choppin, Gregory; Couston, Laurent; Dubois, Veronique; Fanghänel, Thomas; Geipel, Gerhard; Hubert, Solange; Kim, Jae I; Kimura, Takaumi; Klenze, Reinhardt; Kronenberg, Andreas; Kumke, Michael; Lagarde, Gerard; Lamarque, Gerard; Lis, Stefan; Madic, Charles; Meinrath, Gunther; Moulin, Christophe; Nagaishi, Ryuji; Parker, David; Plancque, Gabriel; Scherbaum, Franz; Simoni, Eric; Sinkov, Sergei; Viallesoubranne, Carole

    2003-08-01

    Results of an inter-laboratory round-robin study of the application of time-resolved emission spectroscopy (TRES) to the speciation of uranium(VI) in aqueous media are presented. The round-robin study involved 13 independent laboratories, using various instrumentation and data analysis methods. Samples were prepared based on appropriate speciation diagrams and, in general, were found to be chemically stable for at least six months. Four different types of aqueous uranyl solutions were studied: (1) acidic medium where UO2(2+)aq is the single emitting species, (2) uranyl in the presence of fluoride ions, (3) uranyl in the presence of sulfate ions, and (4) uranyl in aqueous solutions at different pH, promoting the formation of hydrolyzed species. Results between the laboratories are compared in terms of the number of decay components, luminescence lifetimes, and spectral band positions. The successes and limitations of TRES in uranyl analysis and speciation in aqueous solutions are discussed.

  3. Nondestructive identification of ancient Chinese glasses by Raman and proton-induced X-ray emission spectroscopy

    Institute of Scientific and Technical Information of China (English)

    Hongxia Zhao; Huansheng Cheng; Qinghui Li; Fuxi Gan

    2011-01-01

    @@ Nondestructive Raman spectroscopy and external-beam proton-induced X-ray emission (PIXE) technique to analyze eight ancient glasses unearthed from the provinces of Henan, Hubei, and Jiangsu, which allowes for a good characterization of the glass matrix and chemical compositions, is carried out.The results indicate that all the eight glass samples could be typically divided into three systems: faience (sample No.SZWG-4), PbO-BaO-SiO2 (sample Nos.NYWKI-5-1, HNWKII-88, and HNWKII-84), and Na2O-CaO-SiO2 (sample Nos.HBWKI-16, HBWKI-17, HBWKI-18, and SZWG-1).Additional relationships between the Rarnan spectra and parameters, such as residues of raw materials and opacifying agent, are also discussed by respectively comparing them with similar glass samples excavated from other historical sites.%Nondestructive Raman spectroscopy and external-beam proton-induced X-ray emission (PIXE) technique to analyze eight ancient glasses unearthed from the provinces of Henan, Hubei, and Jiangsu, which allowes for a good characterization of the glass matrix and chemical compositions, is carried out.The results indicate that all the eight glass samples could be typically divided into three systems: faience (sample No.SZWG-4), PbO-BaO-SiO2 (sample Nos.NYWKⅠ-5-1, HNWKⅡ-88, and HNWKⅡ-84), and Na2OCaO-SiO2 (sample Nos.HBWKⅠ-16, HBWKⅠ-17, HBWKⅠ-18, and SZWG-1).Additional relationships between the Raman spectra and parameters, such as residues of raw materials and opacifying agent, are also discussed by respectively comparing them with similar glass samples excavated from other historical sites.

  4. Prospects for laser-induced breakdown spectroscopy for biomedical applications: a review.

    Science.gov (United States)

    Singh, Vivek Kumar; Rai, Awadhesh Kumar

    2011-09-01

    We review the different spectroscopic techniques including the most recent laser-induced breakdown spectroscopy (LIBS) for the characterization of materials in any phase (solid, liquid or gas) including biological materials. A brief history of the laser and its application in bioscience is presented. The development of LIBS, its working principle and its instrumentation (different parts of the experimental set up) are briefly summarized. The generation of laser-induced plasma and detection of light emitted from this plasma are also discussed. The merit and demerits of LIBS are discussed in comparison with other conventional analytical techniques. The work done using the laser in the biomedical field is also summarized. The analysis of different tissues, mineral analysis in different organs of the human body, characterization of different types of stone formed in the human body, analysis of biological aerosols using the LIBS technique are also summarized. The unique abilities of LIBS including detection of molecular species and calibration-free LIBS are compared with those of other conventional techniques including atomic absorption spectroscopy, inductively coupled plasma atomic emission spectroscopy and mass spectroscopy, and X-ray fluorescence.

  5. Adsorption, X-ray Diffraction, Photoelectron, and Atomic Emission Spectroscopy Benchmark Studies for the Eighth Industrial Fluid Properties Simulation Challenge*+

    Science.gov (United States)

    Ross, Richard B.; Aeschliman, David B.; Ahmad, Riaz; Brennan, John K.; Brostrom, Myles L.; Frankel, Kevin A.; Moore, Jonathan D.; Moore, Joshua D.; Mountain, Raymond D.; Poirier, Derrick M.; Thommes, Matthias; Shen, Vincent K.; Schultz, Nathan E.; Siderius, Daniel W.; Smith, Kenneth D.

    2016-01-01

    The primary goal of the eighth industrial fluid properties simulation challenge was to test the ability of molecular simulation methods to predict the adsorption of organic adsorbates in activated carbon materials. The challenge focused on the adsorption of perfluorohexane in the activated carbon standard BAM-P109 (Panne and Thünemann 2010). Entrants were challenged to predict the adsorption of perfluorohexane in the activated carbon at a temperature of 273 K and at relative pressures of 0.1, 0.3, and 0.6. The relative pressure (P/Po) is defined as that relative to the bulk saturation pressure predicted by the fluid model at a given temperature (273 K in this case). The predictions were judged by comparison to a set of experimentally determined values, which are published here for the first time and were not disclosed to the entrants prior to the challenge. Benchmark experimental studies, described herein, were also carried out and provided to entrants in order to aid in the development of new force fields and simulation methods to be employed in the challenge. These studies included argon, carbon dioxide, and water adsorption in the BAM-P109 activated carbon as well as X-ray diffraction, X-ray microtomography, photoelectron spectroscopy, and atomic emission spectroscopy studies of BAM-P109. Several concurrent studies were carried out for the BAM-P108 activated carbon (Panne and Thünemann 2010). These are included in the current manuscript for comparison. PMID:27840543

  6. Resonant x-ray emission spectroscopy of liquid water: novel instrumentation, high resolution, and the"map" approach

    Energy Technology Data Exchange (ETDEWEB)

    Weinhardt, L.; Fuchs, O.; Blum, M.; B& #228; r, M.; Weigand, M.; Denlinger, J.D.; Zubavichus, Y.; Zharnikov, M.; Grunze, M.; Heske, C.; Umbach, E.

    2008-06-17

    Techniques to study the electronic structure of liquids are rare. Most recently, resonant x-ray emission spectroscopy (XES) has been shown to be an extremely versatile spectroscopy to study both occupied and unoccupied electronic states for liquids in thermodynamic equilibrium. However, XES requires high-brilliance soft x-ray synchrotron radiation and poses significant technical challenges to maintain a liquid sample in an ultra-high vacuum environment. Our group has therefore developed and constructed a novel experimental setup for the study of liquids, with the long-term goal of investigating the electronic structure of biological systems in aqueous environments. We have developed a flow-through liquid cell in which the liquid is separated from vacuum by a thin Si3N4 or SiC window and which allows a precise control of temperature. This approach has significant advantages compared to static liquids cells used in the past. Furthermore, we have designed a dedicated high-transmission, high-resolution soft x-ray spectrometer. The high transmission makes it possible to measure complete resonant XES"maps" in less than an hour, giving unprecedented detailed insight into the electronic structure of the investigated sample. Using this new equipment we have investigated the electronic structure of liquid water. Furthermore, our XES spectra and maps give information about ultra-fast dissociation on the timescale of the O 1s core hole lifetime, which is strongly affected by the initial state hydrogen bonding configuration.

  7. X-ray emission spectroscopy applied to glycine adsorbed on Cu(110): An atom and symmetry projected view

    Energy Technology Data Exchange (ETDEWEB)

    Hasselstroem, J.; Karis, O.; Weinelt, M. [Uppsala Univ. (Sweden)] [and others

    1997-04-01

    When a molecule is adsorbed on a metal surface by chemical bonding new electronic states are formed. For noble and transition metals these adsorption-induced states overlap with the much more intense metal d-valence band, making them difficult to probe by for instance direct photoemission. However, it has recently been shown that X-ray emission spectroscopy (XES) can be applied to adsorbate systems. Since the intermediate state involves a core hole, this technique has the power to project out the partial density of states around each atomic site. Both the excitation and deexcitation processes are in general governed by the dipole selection rules. For oriented system, it is hence possible to obtain a complete separation into 2p{sub x}, 2p{sub y} and 2p{sub z} contributions using angular resolved measurements. The authors have applied XES together with other core level spectroscopies to glycine adsorption on Cu(110). Glycine (NH{sub 2}CH{sub 2}COOH) is the smallest amino acid and very suitable to study by core level spectroscopy since it has several functional groups, all well separated in energy by chemical shifts. Its properties are futhermore of biological interest. In summary, the authors have shown that it is possible to apply XES to more complicated molecular adsorbates. The assignment of different electronic states is however not as straight forward as for simple diatomic molecules. For a complete understanding of the redistribution and formation of new electronic states associated with the surface chemical bond, experimental data must be compared to theoretical calculations.

  8. Performance testing of multi-metal continuous emissions monitors

    Energy Technology Data Exchange (ETDEWEB)

    Haas, W.J. [Ames Lab., IA (United States); French, N.B. [Sky+, Inc. (United States); Brown, C.H. [Oak Ridge National Lab., TN (United States); Burns, D.B. [Westinghouse Savannah River Co., Aiken, SC (United States); Lemieux, P.M.; Ryan, J.V. [National Risk Management Research Lab., Research Triangle Park, NC (United States); Priebe, S.J. [Idaho National Engineering and Environmental Lab., Idaho Falls, ID (United States); Waterland, L.R. [Acurex Environmental Corp. (United States)

    1997-11-17

    Three prototype multi-metals continuous emissions monitors (CEMs) were tested in April 1996 at the Rotary Kiln Incinerator Simulator facility at the US Environmental Protection Agency (EPA) National Risk Management Research Laboratory, Research Triangle Park, North Carolina. The CEM instruments were: Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES); Laser Induced Breakdown Spectrometry-Atomic Emission Spectroscopy (LIBS); and Laser Spark Spectrometry, another LIBS instrument. The three CEMs were tested simultaneously during test periods in which low, medium, and high concentration levels of seven toxic metals -- antimony, arsenic, beryllium, cadmium, chromium, lead, and mercury -- were maintained under carefully controlled conditions. Two methods were used to introduce the test metals into the flue gas: (1) solution atomization, introducing metal-containing aerosol directly into the secondary combustion burner, and (2) injection of fly ash particulates. The testing addressed four measures of CEM performance: relative accuracy (RA), calibration drift, zero drift, and response time. These were accomplished by comparing the toxic metal analyte concentrations reported by the CEMs to the concentrations measured using the EPA reference method (RM) for the same analytes. Overall, the test results showed the prototype nature of the test CEMs and the clear need for further development. None of the CEMs tested consistently achieved RA values of 20% or less as required by the EPA draft performance specification. Instrument size reduction and automation will also likely need additional attention before multi-metal CEMs systems become commercially available for service as envisioned by regulators and citizens.

  9. Composition variations in Cu{sub 2}ZnSnSe{sub 4} thin films analyzed by X-ray diffraction, energy dispersive X-ray spectroscopy, particle induced X-ray emission, photoluminescence, and Raman spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Nam, Dahyun [Department of Physics, Sogang University, Seoul 121-742 (Korea, Republic of); Opanasyuk, A.S.; Koval, P.V.; Ponomarev, A.G. [Department of Electronics and Computer Technology, Sumy State University, Sumy UA-40007 (Ukraine); Jeong, Ah Reum; Kim, Gee Yeong; Jo, William [Department of Physics, Ewha Womans University, Seoul 120-750 (Korea, Republic of); Cheong, Hyeonsik, E-mail: hcheong@sogang.ac.kr [Department of Physics, Sogang University, Seoul 121-742 (Korea, Republic of)

    2014-07-01

    Compositional and structural studies of Cu{sub 2}ZnSnSe{sub 4} (CZTSe) thin films were carried out by X-ray diffraction, energy dispersive X-ray spectroscopy (EDS), particle induced X-ray emission (PIXE), photoluminescence, and Raman spectroscopy. CZTSe thin films with different compositions were deposited on sodalime glass by co-evaporation. The composition of the films measured by two different methods, EDS and PIXE, showed significant differences. Generally, the Zn/Sn ratio measured by EDS is larger than that measured by PIXE. Both the micro-PIXE and the micro-Raman imaging results indicated the compositional and structural inhomogeneity of the sample. - Highlights: • Particle induced X-ray emission was used to analyze the composition of CZTSe films. • Energy dispersive X-ray spectroscopy tends to underestimate the Sn composition. • Local Raman intensity is related with the composition rather than the crystallinity.

  10. Atmospheric Longwave Infrared Emission Spectroscopy of Water Vapor at the South Pole

    OpenAIRE

    Myers, Brooke A.

    2000-01-01

    The downward infrared radiance spectrum was measured with a Michelson Long Wave Infrared (LWIR) spectrometer at the Amundsen-Scott South Pole Station. Spectra were collected year-round at the South Pole in 1998. This research focuses on the atmospheric water emission lines between 250 and 800 cm-1 (40 to 12.5 μm) region. The spectral resolution is 1 cm-1. The atmosphere over the South Pole is the driest and coldest on Earth. Winter surface temperatures average approximately -60°C, while the t...

  11. Determination of phosphorus in lubricating oils by cool-flame emission spectroscopy.

    Science.gov (United States)

    Elliott, W N; Heathcote, C; Mostyn, R A

    1972-03-01

    The phosphorus content of lubricating oils is determined by measurement of the emission from the HPO molecular species at 528 nm in a cool hydrogen-nitrogen diffusion flame. The oil is ashed in the presence of potassium hydroxide and an aqueous extract of the melt is treated with ion-exchange resin to remove interferents, before aspiration into the flame. Analytical results are presented on samples containing phosphorus in the range 0.009-0.2%. The precision of the method is +/- 5% at the 0.04% phosphorus level.

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

    Directory of Open Access Journals (Sweden)

    Arzu AKPINAR-BAYIZIT

    2010-12-01

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

  13. Evaluation of cross-sections for particle induced gamma-ray emission (PIGE) spectroscopy

    Science.gov (United States)

    Gurbich, A. F.

    2014-07-01

    The extension of the cross-section evaluation procedure to PIGE data was investigated and the first results are reported. Two different cases were studied: the gamma emission accompanying inelastic scattering of protons, and the (p,γ)-reaction. The corresponding theoretical calculations were performed in the framework of R-matrix and DWBA for the (p,p‧γ) reaction on 23Na, and using statistical model for the proton radiative capture by 52Cr. The possibility of achieving a close fit to the experimental data is demonstrated.

  14. Evaluation of cross-sections for particle induced gamma-ray emission (PIGE) spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Gurbich, A.F., E-mail: gurbich@ippe.ru

    2014-07-15

    The extension of the cross-section evaluation procedure to PIGE data was investigated and the first results are reported. Two different cases were studied: the gamma emission accompanying inelastic scattering of protons, and the (p,γ)-reaction. The corresponding theoretical calculations were performed in the framework of R-matrix and DWBA for the (p,p′γ) reaction on {sup 23}Na, and using statistical model for the proton radiative capture by {sup 52}Cr. The possibility of achieving a close fit to the experimental data is demonstrated.

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

    OpenAIRE

    Muramatsu, Yasuji

    2009-01-01

    To analyze the local structure and/or chemical states of boron atoms in boron-doped diamond, which can be synthesized by the microwave plasma-assisted chemical vapor deposition method (CVD-B-diamond) and the temperature gradient method at high pressure and high temperature (HPT-B-diamond), we measured the soft X-ray emission spectra in the CK and BK regions of B-diamonds using synchrotron radiation at the Advanced Light Source (ALS). X-ray spectral analyses using the fingerprint method and mo...

  16. Comparison Between X-rays Absorption and Emission Spectroscopy Measurements on a Ceramic Envelop Lamp

    Institute of Scientific and Technical Information of China (English)

    Bruno LAFITTE; Michel AUBES; Georges ZISSIS

    2007-01-01

    Burners of metal halide lamps used for illumination are generally made of polycrystalline alumina ceramic (PCA) which is translucent to visible light.We show that the difficulty of selecting a line of sight through the lamp prevents the use of optical emission diagnostic.X-rays photons are mainly absorbed and not scattered by PCA.Absorption by mercury atoms contributing to the discharge allowed us to determine the density of mercury in the lamp.By comparing diagnostic methods,we put in evidence the difficulty of taking into account the scattering of light mathematically.

  17. Study of argon additive in a beam injection type negative ion source using VUV emission spectroscopy

    OpenAIRE

    Nakada, Naoki; Fukumasa, Osamu

    2006-01-01

    Effects of Ar addition are studied by using a beam injection type negative ion source. With adding Ar, I_ increases at low base H_2 pressure. At high base H_2 pressure, however, I_ decreases. VUV emission intensities also decrease at high base pressure. In other words, Ar addition is adverse effect for production of H_2 (v''). Therefore, decrease in I_ is caused by decrease in H_2 (v''). In D_2 plasmas, variation patterns of plasma parameters and VUV intensities by Ar addition are nearly the ...

  18. Further evidence for charge transfer complexes in brown carbon aerosols from excitation-emission matrix fluorescence spectroscopy.

    Science.gov (United States)

    Phillips, Sabrina M; Smith, Geoffrey D

    2015-05-14

    The light-absorbing fraction of organic molecules in ambient aerosols, known as "brown carbon," is an important yet poorly characterized component. Despite the fact that brown carbon could alter the radiative forcing of aerosols significantly, identification of specific chromophores has remained challenging. We recently demonstrated that charge transfer (CT) complexes formed in organic molecules could be responsible for a large fraction of absorption observed in water-extracted ambient particulate matter.1 In the present study, we use excitation-emission matrix fluorescence spectroscopy to further corroborate the importance of CT complexes in defining aerosol optical properties. Monotonically increasing and decreasing quantum yields, decreasing Stokes shifts, and red-shifting emission maxima are observed from ambient particulate matter collected in Athens, Georgia, strongly suggesting that a superposition of independent chromophores is not sufficient to explain brown carbon absorption and fluorescence. Instead, we show that a model in which such chromophores are energetically coupled to a dense manifold of CT complexes is consistent with all of the observations. Further, we suggest that a significant fraction of the observed fluorescence originates from CT complexes and that their contribution to brown carbon absorption is likely greater than we reported previously.

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

    Science.gov (United States)

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

    2012-01-16

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

  20. Characterization of direct current He-N{sub 2} mixture plasma using optical emission spectroscopy and mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Flores, O.; Castillo, F.; Martinez, H. [Laboratorio de Espectroscopia, Instituto de Ciencias Físicas, Universidad Nacional Autónoma de México, Apartado Postal 48-3, 62251, Cuernavaca, Morelos (Mexico); Villa, M.; Reyes, P. G. [Facultad de Ciencias, Universidad Autónoma del Estado de México, Estado de México (Mexico); Villalobos, S. [Laboratorio de Espectroscopia, Instituto de Ciencias Físicas, Universidad Nacional Autónoma de México, Apartado Postal 48-3, 62251, Cuernavaca, Morelos (Mexico); Facultad de Ingeniería, Universidad Nacional Autónoma de México, México D.F. (Mexico)

    2014-05-15

    This study analyses the glow discharge of He and N{sub 2} mixture at the pressure of 2.0 Torr, power of 10 W, and flow rate of 16.5 l/min, by using optical emission spectroscopy and mass spectrometry. The emission bands were measured in the wavelength range of 200–1100 nm. The principal species observed were N{sub 2}{sup +} (B{sup 2}Σ{sup +}{sub u}→X{sup 2}Σ{sup +}{sub g}), N{sub 2} (C{sup 3}Π{sub u}→B{sup 3}Π{sub g}), and He, which are in good agreement with the results of mass spectrometry. Besides, the electron temperature and ion density were determined by using a double Langmuir probe. Results indicate that the electron temperature is in the range of 1.55–2.93 eV, and the electron concentration is of the order of 10{sup 10} cm{sup −3}. The experimental results of electron temperature and ion density for pure N{sub 2} and pure He are in good agreement with the values reported in the literature.

  1. Physical Properties of Emission-Line Galaxies at z ~ 2 from Near-Infrared Spectroscopy with Magellan FIRE

    CERN Document Server

    Masters, Daniel; Siana, Brian; Malkan, Matthew; Mobasher, Bahram; Atek, Hakim; Henry, Alaina; Martin, Crystal L; Rafelski, Marc; Hathi, Nimish P; Scarlata, Claudia; Ross, Nathaniel R; Bunker, Andrew J; Blanc, Guillermo A; Bedregal, Alejandro G; Dominguez, Alberto; Colbert, James; Teplitz, Harry; Dressler, Alan

    2014-01-01

    We present results from near-infrared spectroscopy of 26 emission-line galaxies at z ~ 2 obtained with the FIRE spectrometer on the Magellan Baade telescope. The sample was selected from the WISP survey, which uses the near-infrared grism of the Hubble Space Telescope Wide Field Camera 3 to detect emission-line galaxies over 0.3 1 star-forming galaxies, but composite spectra derived from the sample do not show an appreciable offset from the local star-forming sequence on the [O III]/H-beta versus [S II]/H-alpha diagram. We infer a high nitrogen-to-oxygen abundance ratio from the composite spectrum, which may contribute to the offset of the high-redshift galaxies from the local star-forming sequence in the [O III]/H-beta versus [N II]/H-alpha diagram. We speculate that the elevated nitrogen abundance could result from substantial numbers of Wolf-Rayet stars in starbursting galaxies at z~2. (Abridged)

  2. The Nature of Extreme Emission Line Galaxies at z=1-2: Kinematics and Metallicities from Near-Infrared Spectroscopy

    CERN Document Server

    Maseda, Michael V; Rix, Hans-Walter; da Cunha, Elisabete; Pacifici, Camilla; Momcheva, Ivelina; Brammer, Gabriel B; Meidt, Sharon E; Franx, Marijn; van Dokkum, Pieter; Fumagalli, Mattia; Bell, Eric F; Ferguson, Henry C; Förster-Schreiber, Natascha M; Koekemoer, Anton M; Koo, David C; Lundgren, Britt F; Marchesini, Danilo; Nelson, Erica J; Patel, Shannon G; Skelton, Rosalind E; Straughn, Amber N; Trump, Jonathan R; Whitaker, Katherine E

    2014-01-01

    We present near-infrared spectroscopy of a sample of 22 Extreme Emission Line Galaxies at redshifts 1.3 5) and [N II]/H{\\alpha} is always significantly below unity, which suggests a low gas-phase metallicity. We are able to determine gas-phase metallicities for 7 of our objects using various strong-line methods, with values in the range 0.05-0.30 Z_sun and with a median of 0.15 Z_sun; for 3 of these objects we detect [O III]{\\lambda}4363 which allows for a direct constraint on the metallicity. The velocity dispersion, as measured from the nebular emission lines, is typically ~50 km/s. Combined with the observed star-forming activity, the Jeans and Toomre stability criteria imply that the gas fraction must be large (> 2/3), consistent with the difference between our dynamical and stellar mass estimates. The implied gas depletion time scale (several hundred Myr) is substantially longer than the inferred mass-weighted ages (~50 Myr), which further supports the emerging picture that most stars in low-mass galaxi...

  3. Fast Detection Allows Analysis of the Electronic Structure of Metalloprotein by X-ray Emission Spectroscopy at Room Temperature.

    Science.gov (United States)

    Davis, Katherine M; Mattern, Brian A; Pacold, Joseph I; Zakharova, Taisiya; Brewe, Dale; Kosheleva, Irina; Henning, Robert W; Graber, Timothy J; Heald, Steve M; Seidler, Gerald T; Pushkar, Yulia

    2012-07-19

    The paradigm of "detection-before-destruction" was tested for a metalloprotein complex exposed at room temperature to the high x-ray flux typical of third generation synchrotron sources. Following the progression of the x-ray induced damage by Mn Kβ x-ray emission spectroscopy, we demonstrated the feasibility of collecting room temperature data on the electronic structure of native Photosystem II, a trans-membrane metalloprotein complex containing a Mn(4)Ca cluster. The determined non-damaging observation timeframe (about 100 milliseconds using continuous monochromatic beam, deposited dose 1*10(7) photons/µm(2) or 1.3*10(4) Gy, and 66 microseconds in pulsed mode using pink beam, deposited dose 4*10(7) photons/µm(2) or 4.2*10(4) Gy) is sufficient for the analysis of this protein's electron dynamics and catalytic mechanism at room temperature. Reported time frames are expected to be representative for other metalloproteins. The described instrumentation, based on the short working distance dispersive spectrometer, and experimental methodology is broadly applicable to time-resolved x-ray emission analysis at synchrotron and x-ray free-electron laser light sources.

  4. Extended wavelength anisotropy resolved multidimensional emission spectroscopy (ARMES) measurements: better filters, validation standards, and Rayleigh scatter removal methods

    Science.gov (United States)

    Casamayou-Boucau, Yannick; Ryder, Alan G.

    2017-09-01

    Anisotropy resolved multidimensional emission spectroscopy (ARMES) provides valuable insights into multi-fluorophore proteins (Groza et al 2015 Anal. Chim. Acta 886 133-42). Fluorescence anisotropy adds to the multidimensional fluorescence dataset information about the physical size of the fluorophores and/or the rigidity of the surrounding micro-environment. The first ARMES studies used standard thin film polarizers (TFP) that had negligible transmission between 250 and 290 nm, preventing accurate measurement of intrinsic protein fluorescence from tyrosine and tryptophan. Replacing TFP with pairs of broadband wire grid polarizers enabled standard fluorescence spectrometers to accurately measure anisotropies between 250 and 300 nm, which was validated with solutions of perylene in the UV and Erythrosin B and Phloxine B in the visible. In all cases, anisotropies were accurate to better than ±1% when compared to literature measurements made with Glan Thompson or TFP polarizers. Better dual wire grid polarizer UV transmittance and the use of excitation-emission matrix measurements for ARMES required complete Rayleigh scatter elimination. This was achieved by chemometric modelling rather than classical interpolation, which enabled the acquisition of pure anisotropy patterns over wider spectral ranges. In combination, these three improvements permit the accurate implementation of ARMES for studying intrinsic protein fluorescence.

  5. A synthetic diagnostic for beam emission spectroscopy in the helically symmetric experiment stellarator

    Science.gov (United States)

    Dobbins, T. J.; Kumar, S. T. A.; Anderson, D. T.

    2016-11-01

    The Helically Symmetric Experiment (HSX) has a number of active spectroscopy diagnostics. Due to the relatively large beam width compared to the plasma minor radius, it is difficult to achieve good spatial resolution at the core of the HSX plasma. This is due to the fact that the optical sightline cuts through many flux surfaces with varying field vectors within the beam. In order to compare the experimental results with theoretical models it is important to accurately model the beam width effects. A synthetic diagnostic has been developed for this purpose. This synthetic diagnostic calculates the effect of spot size and beam width on the measurements of quantities of interest, including radial electric field, flow velocity, and Stark polarization.

  6. Glow discharge optical emission spectroscopy for accurate and well resolved analysis of coatings and thin films

    KAUST Repository

    Wilke, Marcus

    2011-12-01

    In the last years, glow discharge optical emission spectrometry (GDOES) gained more and more acceptance in the analysis of functional coatings. GDOES thereby represents an interesting alternative to common depth profiling techniques like AES and SIMS, based on its unique combination of high erosion rates and erosion depths, sensitivity, analysis of nonconductive layers and easy quantification even for light elements such as C, N, O and H. Starting with the fundamentals of GDOES, a short overview on new developments in instrument design for accurate and well resolved thin film analyses is presented. The article focuses on the analytical capabilities of glow discharge optical emission spectrometry in the analysis of metallic coatings and thin films. Results illustrating the high depth resolution, confirmation of stoichiometry, the detection of light elements in coatings as well as contamination on the surface or interfaces will be demonstrated by measurements of: a multilayer system Cr/Ti on silicon, interface contamination on silicon during deposition of aluminum, Al2O3-nanoparticle containing conversion coatings on zinc for corrosion resistance, Ti3SiC2 MAX-phase coatings by pulsed laser deposition and hydrogen detection in a V/Fe multilayer system. The selected examples illustrate that GDOES can be successfully adopted as an analytical tool in the development of new materials and coatings. A discussion of the results as well as of the limitations of GDOES is presented. © 2011 Elsevier B.V.

  7. Suzaku Spectroscopy Study of Hard X-Ray Emission in the Arches Cluster

    CERN Document Server

    Tsujimoto, M; Koyama, K

    2006-01-01

    We present the results of a Suzaku study of the Arches cluster. A high S/N spectrum in the 3-12 keV band was obtained with the XIS. We found that the spectrum consists of a thermal plasma, a hard power-law tail, and two Gaussian lines. The plasma component (kT~2.2 keV) is established from the presence of CaXIX and FeXXV K alpha lines as well as the absence of FeXXVI K alpha line. The two Gaussian lines represent the K alpha and beta lines from iron at lower ionization stages. Both the line centers and the intensity ratio of these two lines are consistent with the neutral iron. The hard power-law tail (index~0.7) was found to have no pronounced iron K edge feature. In comparison with the published Chandra spectra, we conclude that the thermal component is from the ensemble of point-like sources plus thermal diffuse emission concentrated at the cluster center, while the Gaussian and the hard tail components are from the non-thermal diffuse emission extended in a larger scale. In the band-limited XIS images, the...

  8. IFU Spectroscopy of 10 ETG nuclei: Properties of the circumnuclear gas emission

    Science.gov (United States)

    Ricci, T. V.

    2015-09-01

    LINERs are galactic nuclei containing spectra with prominence of low-ionization lines. Several ionization sources are able to produce a LINER-like spectra (e.g. shocks, low-luminosity AGNs, pAGB stars). In this work, we will present an analysis performed on a sample of 10 massive ETGs with distances up to 30 Mpc. This sample was observed with the GMOS-IFU installed on the Gemini-South Telescope. The data cubes of the galaxies have a FOV of 3.5 - 5 arcsec2 and a spatial resolution of about 0.6 -- 1.0 arcsec. After subtracting the stellar component of the galaxies by means of spectral synthesis, we studied the emission lines all over the FOV of the data cubes. In galaxies where an AGN was clearly detected, we found ionized gaseous discs and also a low-velocity extended emission perpendicular to the gas discs. We concluded that only ionizing photons emerging from the AGNs are not enough to photoionize the gaseous discs of the galaxies. On the other hand, it seems to be responsible for the photoionization of the low-velocity extended gas perpendicular to the discs. We propose a scheme where some collimating agent, somehow aligned to the gaseous discs, may be present in some LINER-like AGNs in the local universe.

  9. Field emission spectroscopy evidence for dual-barrier electron tunnelling in nanographite

    Energy Technology Data Exchange (ETDEWEB)

    Bandurin, D. A.; Kleshch, V. I. [Department of Physics, M.V. Lomonosov Moscow State University, Moscow 119991 (Russian Federation); Mingels, S.; Lützenkirchen-Hecht, D.; Müller, G. [FB C Physics Department, University of Wuppertal, 42119 Wuppertal (Germany); Obraztsov, A. N., E-mail: obraz@polly.phys.msu.ru [Department of Physics, M.V. Lomonosov Moscow State University, Moscow 119991 (Russian Federation); Department of Physics and Mathematics, University of Eastern Finland, Joensuu 80101 (Finland)

    2015-06-08

    Nanocarbon films with upstanding flake-like graphite crystallites of nanometre thickness were fabricated by carbon condensation from a methane–hydrogen gas mixture activated by a direct-current discharge. The nanographite (NG) crystallites are composed of a few graphene layers. The adjacent atomic layers are connected partially at the edges of the crystallites to form strongly curved graphene structures. The extraordinary field emission (FE) properties were revealed for the NG films with an average current density of a few mA/cm{sup 2}, reproducibly obtained at a macroscopic applied field of about 1 V/μm. The integral FE current–voltage curves and electron spectra (FEES) of NG cathodes with multiple emitters were measured in a triode configuration. Most remarkably, above a threshold field, two peaks were revealed in FEES with different field-dependent shifts to lower energies. This behaviour evidences electron emission through a dual potential barrier, corresponding to carbon–carbon heterostructure formed as a result of the graphene bending.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-02-15

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

  11. Spectroscopy of southern Galactic disk planetary nebulae. Notes on chemical composition and emission-line stars

    CERN Document Server

    Górny, S K

    2014-01-01

    We present low resolution spectroscopic observations for a sample of 53 planetary nebulae (PNe) located in the southern sky between Vela and Norma constellations and pertaining to the Galactic disk with expected Galactocentric distance range of 5 to 10 kpc. We derive nebular chemical composition and plasma parameters with the classical empirical method. For most of the observed objects it is done for the first time. The distributions of the chemical abundances of the observed disk sample are generally indistinguishable from Galactic bulge and inner-disk PNe populations. The exceptions are possible differences in He/H distribution comparing to bulge PNe and Ne/Ar comparing to inner-disk PNe sample. The derived O/H ratios for the observed disk PNe fit to the concept of flattening of the chemical gradient in the inner parts of the Milky Way. We use the spectra to search for emission-line central stars in the observed sample. We found 6 new emission-line central stars comprising examples of all known types: WEL, ...

  12. Investigation of local thermodynamic equilibrium of laser induced Al2O3-TiC plasma in argon by spatially resolved optical emission spectroscopy

    Science.gov (United States)

    Alnama, K.; Alkhawwam, A.; Jazmati, A. K.

    2016-06-01

    Plasma plume of Al2O3-TiC is generated by third harmonic Q-switched Nd:YAG nanosecond laser. It is characterized using Optical Emission Spectroscopy (OES) at different argon background gas pressures 10, 102, 103, 104 and 105 Pa. Spatial evolution of excitation and ionic temperatures is deduced from spectral data analysis. Temporal evolution of Ti I emission originated from different energy states is probed. The correlation between the temporal behavior and the spatial temperature evolution are investigated under LTE condition for the possibility to use the temporal profile of Ti I emission as an indicator for LTE validity in the plasma.

  13. Investigation of local thermodynamic equilibrium of laser induced Al2O3–TiC plasma in argon by spatially resolved optical emission spectroscopy

    Directory of Open Access Journals (Sweden)

    K. Alnama

    2016-06-01

    Full Text Available Plasma plume of Al2O3–TiC is generated by third harmonic Q-switched Nd:YAG nanosecond laser. It is characterized using Optical Emission Spectroscopy (OES at different argon background gas pressures 10, 102, 103, 104 and 105 Pa. Spatial evolution of excitation and ionic temperatures is deduced from spectral data analysis. Temporal evolution of Ti I emission originated from different energy states is probed. The correlation between the temporal behavior and the spatial temperature evolution are investigated under LTE condition for the possibility to use the temporal profile of Ti I emission as an indicator for LTE validity in the plasma.

  14. Resonant X-ray emission spectroscopy reveals d-d ligand-field states involved in the self-assembly of a square-planar platinum complex.

    Science.gov (United States)

    Garino, Claudio; Gallo, Erik; Smolentsev, Nikolay; Glatzel, Pieter; Gobetto, Roberto; Lamberti, Carlo; Sadler, Peter J; Salassa, Luca

    2012-11-28

    Resonant X-ray Emission Spectroscopy (RXES) is used to characterize the ligand field states of the prototypic self-assembled square-planar complex, [Pt(tpy)Cl]Cl (tpy=2,2':6',2''-terpyridine), and determine the effect of weak metal-metal and π-π interactions on their energy.

  15. Exoplanet atmosphere. Thermal structure of an exoplanet atmosphere from phase-resolved emission spectroscopy.

    Science.gov (United States)

    Stevenson, Kevin B; Désert, Jean-Michel; Line, Michael R; Bean, Jacob L; Fortney, Jonathan J; Showman, Adam P; Kataria, Tiffany; Kreidberg, Laura; McCullough, Peter R; Henry, Gregory W; Charbonneau, David; Burrows, Adam; Seager, Sara; Madhusudhan, Nikku; Williamson, Michael H; Homeier, Derek

    2014-11-14

    Exoplanets that orbit close to their host stars are much more highly irradiated than their solar system counterparts. Understanding the thermal structures and appearances of these planets requires investigating how their atmospheres respond to such extreme stellar forcing. We present spectroscopic thermal emission measurements as a function of orbital phase ("phase-curve observations") for the highly irradiated exoplanet WASP-43b spanning three full planet rotations using the Hubble Space Telescope. With these data, we construct a map of the planet's atmospheric thermal structure, from which we find large day-night temperature variations at all measured altitudes and a monotonically decreasing temperature with pressure at all longitudes. We also derive a Bond albedo of 0.18(-0.12)(+0.07) and an altitude dependence in the hot-spot offset relative to the substellar point.

  16. Thermal structure of an exoplanet atmosphere from phase-resolved emission spectroscopy

    CERN Document Server

    Stevenson, Kevin B; Line, Michael R; Bean, Jacob L; Fortney, Jonathan J; Showman, Adam P; Kataria, Tiffany; Kreidberg, Laura; McCullough, Peter R; Henry, Gregory W; Charbonneau, David; Burrows, Adam; Seager, Sara; Madhusudhan, Nikku; Williamson, Michael H; Homeier, Derek

    2014-01-01

    Exoplanets that orbit close to their host stars are much more highly irradiated than their Solar System counterparts. Understanding the thermal structures and appearances of these planets requires investigating how their atmospheres respond to such extreme stellar forcing. We present spectroscopic thermal emission measurements as a function of orbital phase ("phase-curve observations") for the highly-irradiated exoplanet WASP-43b spanning three full planet rotations using the Hubble Space Telescope. With these data, we construct a map of the planet's atmospheric thermal structure, from which we find large day-night temperature variations at all measured altitudes and a monotonically decreasing temperature with pressure at all longitudes. We also derive a Bond albedo of 0.18 +0.07,-0.12 and an altitude dependence in the hot-spot offset relative to the substellar point.

  17. Determination of the electron energy distribution function of a low temperature plasma from optical emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Dodt, Dirk Hilar

    2009-01-05

    The experimental determination of the electron energy distribution of a low pressure glow discharge in neon from emission spectroscopic data has been demonstrated. The spectral data were obtained with a simple overview spectrometer and analyzed using a strict probabilistic, Bayesian data analysis. It is this Integrated Data Analysis (IDA) approach, which allows the significant extraction of non-thermal properties of the electron energy distribution function (EEDF). The results bear potential as a non-invasive alternative to probe measurements. This allows the investigation of spatially inhomogeneous plasmas (gradient length smaller than typical probe sheath dimensions) and plasmas with reactive constituents. The diagnostic of reactive plasmas is an important practical application, needed e.g. for the monitoring and control of process plasmas. Moreover, the experimental validation of probe theories for magnetized plasmas as a long-standing topic in plasma diagnostics could be addressed by the spectroscopic method. (orig.)

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

    Science.gov (United States)

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

    2016-03-01

    Particle-Induced Gamma-ray Emission (PIGE) is a powerful analytical technique that exploits the interactions of rapid charged particles with nuclei located near a sample surface to determine the composition and structure of the surface regions of solids by measurement of characteristic prompt γ rays. The potential for depth profiling of this technique has long been recognized, however, the implementation has been limited owing to insufficient knowledge of the physical data and lack of suitable user-friendly computer codes for the applications. Although a considerable body of published data exists in the nuclear physics literature for nuclear reaction cross sections with γ rays in the exit channel, there is no up-to-date, comprehensive compilation specifically dedicated to IBA applications. A number of PIGE cross-section data had already been uploaded to the Ion Beam Analysis Nuclear Data Library (IBANDL)

  19. Determination of ammonium and organic bound nitrogen by inductively coupled plasma emission spectroscopy.

    Science.gov (United States)

    Jaber, A M Y; Mehanna, N A; Sultan, S M

    2009-06-15

    The continuous flow sample introduction technique with a hydride generator system in conjunction with an inductively coupled plasma emission spectrometer (ICP-AES-HG), is used in this study for quantitative determination of ammonium and organic bound nitrogen in aqueous and solid samples. Ammonia vapor released from ammonium salt after treatment with concentrated NaOH is transferred by argon to plasma for detection at 174.273 nm using axial argon plasma mode. The calibration curves were linear within a range of 25-1000 mg L(-1)N as ammonium molybdate with correlation coefficients of better than 0.99 and limits of detection of about 10-25mg L(-1)N. The percent recovery of N (25-500 mg L(-1)N) in soft (distilled) water and high salt content (1.7 mol L(-1) NaCl) matrices was found to be in the range of about 97-102% with %RSD in the range of 4.6-0.62. The sensitivity, limit of detection, and blank contribution from the atmospheric nitrogen, were tremendously improved in this method compared with the available ICP-AES spray chamber counterpart. Furthermore, the ICP-AES-HG method gave results for real samples (soil, fertilizer, waste water) containing about 50-1800 mg L(-1)N in good agreement with those obtained by the standard Kjeldahl method. No statistical differences at the 95% confidence level on applying the t-test were observed between the values obtained by the two methods. Thus, the ICP-AES-HG method is reliable and faster than the conventional tedious Kjeldahl method, superior to the ICP-AES spray chamber method, and almost free from matrix interference which is usually a critical factor in atomic emission spectroscopic techniques.

  20. Single and double core-hole ion emission spectroscopy of transient neon plasmas produced by ultraintense x-ray laser pulses

    Science.gov (United States)

    Gao, Cheng; Zeng, Jiaolong; Yuan, Jianmin

    2016-05-01

    Single core-hole (SCH) and double core-hole (DCH) spectroscopy is investigated systematically for neon gas in the interaction with ultraintense x-ray pulses with photon energy from 937 eV to 2000 eV. A time-dependent rate equation, implemented in the detailed level accounting approximation, is utilized to study the dynamical evolution of the level population and emission properties of the laser-produced highly transient plasmas. The plasma density effects on level populations are demonstrated with an x-ray photon energy of 2000 eV. For laser photon energy in the range of 937 - 1360 eV, resonant absorptions (RA) of 1s-np (n> = 2) transitions play important roles in time evolution of the population and DCH emission spectroscopy. For x-ray photon energy larger than 1360 eV, no RA exist and transient plasmas show different features in the DCH spectroscopy.

  1. Measuring reactive nitrogen emissions from point sources using visible spectroscopy from aircraft.

    Science.gov (United States)

    Melamed, M L; Solomon, S; Daniel, J S; Langford, A O; Portmann, R W; Ryerson, T B; Nicks, D K; McKeen, S A

    2003-02-01

    Accurate measurements of nitrogen dioxide (NO2), a key trace gas in the formation and destruction of tropospheric ozone, are important in studies of urban pollution. Nitrogen dioxide column abundances were measured during the Texas Air Quality Study 2000 using visible absorption spectroscopy from an aircraft. The method allows for quantification of the integrated total number of nitrogen dioxide molecules in the polluted atmosphere and is hence a useful tool for measuring plumes of this key trace gas. Further, we show how such remote-sensing observations can be used to obtain information on the fluxes of nitrogen dioxide into the atmosphere with unique flexibility in terms of aircraft altitude, and the height and extent of mixing of the boundary layer. Observations of nitrogen dioxide plumes downwind of power plants were used to estimate the flux of nitrogen oxide emitted from several power plants in the Houston and Dallas metropolitan areas and in North Carolina. Measurements taken over the city of Houston were also employed to infer the total flux from the city as a whole.

  2. Source fingerprint monitoring of air pollutants from petrochemical industry and the determination of their annual emission flux using open path Fourier transform infrared spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Yih-Shiaw Huang; Shih-Yi Chang; Tai-Ly Tso [National Tsing Hua Univ., Hsinchu (China)

    1996-12-31

    Toxic air pollutants were investigated in several petrochemical industrial park in Taiwan using a movable open-path Fourier-transform infrared spectroscopy (FTIR). The results show the qualitative and quantitative analysis of emission gases from plants, and also provide the emission rates of various compounds. More than twenty compounds under usual operation were found from these industrial park. The concentration variation with time could be correlated exactly with the distances from the emission source along the wind direction. This means that by changing the measuring points the source of emission could be unambiguously identified. The point, area and line source (PAL) plume dispersion model has been applied to estimate the emission rate of either a point or an area source. The local atmospheric stability was determined by releasing an SF{sub 6} tracer. The origin of errors came mainly from the uncertainty of the source configuration and the variation of the meteorological condition. Through continuous measurement using a portable open-path Fourier transform infrared (POP-FTIR) spectrometer, the maximum value of the emission rate and the annual amount of emission could be derived. The emission rate of the measured toxic gases was derived by the model technique, and the results show that the emission amount is on the order of ten to hundred tons per year.

  3. Development of wavelength-dispersive soft X-ray emission spectrometers for transmission electron microscopes--an introduction of valence electron spectroscopy for transmission electron microscopy.

    Science.gov (United States)

    Terauchi, Masami; Koike, Masato; Fukushima, Kurio; Kimura, Atsushi

    2010-01-01

    Two types of wavelength-dispersive soft X-ray spectrometers, a high-dispersion type and a conventional one, for transmission electron microscopes were constructed. Those spectrometers were used to study the electronic states of valence electrons (bonding electrons). Both spectrometers extended the acceptable energy regions to higher than 2000 eV. The best energy resolution of 0.08 eV was obtained for an Al L-emission spectrum by using the high-dispersion type spectrometer. By using the spectrometer, C K-emission of carbon allotropes, Cu L-emission of Cu(1-x)Zn(x) alloys and Pt M-emission spectra were presented. The FWHM value of 12 eV was obtained for the Pt Malpha-emission peak. The performance of the conventional one was also presented for ZnS and a section specimen of a multilayer device. W-M and Si-K emissions were clearly resolved. Soft X-ray emission spectroscopy based on transmission electron microscopy (TEM) has an advantage for obtaining spectra from a single crystalline specimen with a defined crystal setting. As an example of anisotropic soft X-ray emission, C K-emission spectra of single crystalline graphite with different crystal settings were presented. From the spectra, density of states of pi- and sigma-bondings were separately derived. These results demonstrated a method to analyse the electronic states of valence electrons of materials in the nanometre scale based on TEM.

  4. Measuring PAH Emission in Ultradeep Spitzer IRS Spectroscopy of High Redshift IR Luminous Galaxies

    CERN Document Server

    Teplitz, H I; Armus, L; Chary, R; Marshall, J A; Colbert, J W; Frayer, D T; Pope, A; Blain, A; Spoon, H; Charmandaris, V; Scott, D

    2007-01-01

    The study of the dominant population of high redshift IR-luminous galaxies (10^11 - 10^12 Lsun at 1emission in all four targets, and compare the spectra to those of local galaxies observed by the IRS. The z=1.09 source appears to be a typical, star-formation dominated IR-luminous galaxy, while the z=2.69 source is a composite source with strong star formation and a prominent AGN. The IRAC colors of this source show no evidence of rest-frame near-infrared stellar photospheric...

  5. Emission spectroscopy of an atmospheric pressure plasma jet operated with air at low frequency

    Science.gov (United States)

    Giuliani, L.; Gallego, J. L.; Minotti, F.; Kelly, H.; Grondona, D.

    2015-03-01

    Low-temperature, high-pressure plasma jets have an extensive use in plasma biology and plasma medicine, such as pathogen deactivation, wound disinfection, stopping of bleeding without damage of healthy tissue, acceleration of wound healing, control of bio-film proliferation, etc. In this work, a spectroscopic characterization of a typical plasma jet, operated in air at atmospheric pressure, is reported. Within the spectrum of wavelengths from 200 to 450 nm all remarkable emissions of N2 were monitored. Spectra of the N2 2nd positive system (C3Πu-B3Πg) emitted in air are the most convenient for plasma diagnostics, since they enable to determine electronic Te, rotational Tr and vibrational Tv temperatures by fitting the experimental spectra with the simulated ones. We used SPECAIR software for spectral simulation and obtained the best fit with all these temperatures about 3500K. The conclusion that all temperatures are equal, and its relatively high value, is consistent with the results of a previous work, where it was found that the experimentally determined electrical characteristic was consistent with the model of a thermal arc discharge, together with a highly collisional cathode sheet.

  6. Changes in dissolved organic matter quality in a northern hardwood forest revealed by excitation emission spectroscopy

    Science.gov (United States)

    Saraceno, J.; Shanley, J. B.; Pellerin, B. A.; Hansen, A. M.

    2016-12-01

    Changes in dissolved organic matter (DOM) quality may result from unusual and extreme precipitation patterns such as floods and droughts. In order to study DOM quality changes, we collected several hundred surface water samples during the past eight years from the W-9 watershed of the Sleepers River Research Watershed in Danville, Vermont for optical analysis of dissolved organic matter. We present the results of parallel factor (PARAFAC) and principal component analysis (PCA) on excitation emission matrices (EEMs). This analysis revealed that peaks T, C and M as identified by PARAFAC were the most prominent EEM features. The intensity of these peaks varied on inter-annual, seasonal and event time periods and these shifts reflect changes in DOM quality. Likely drivers of this variability in DOM chemistry are seasonal shifts in flow paths, antecedent moisture conditions, and precipitation duration and intensity. For example, during events, the relative proportion of protein-like, peak T fluorophores increased, likely from flushing of fresh polyphenols from surficial and shallow flow paths. During the winter, when groundwater dominates flow, EEMs were strong in humic-like peak C and peak M fluorophores, reflecting deeper soil sources and longer flow paths. Our analyses will reveal how DOM quality responds to climatic drivers, and thus how we can expect DOM quality to evolve under projected climate change scenarios.

  7. Vibrational Motions Associated with Primary Processes in Bacteriorhodopsin Studied by Coherent Infrared Emission Spectroscopy

    Science.gov (United States)

    Groma, Géza I.; Colonna, Anne; Martin, Jean-Louis; Vos, Marten H.

    2011-01-01

    The primary energetic processes driving the functional proton pump of bacteriorhodopsin take place in the form of complex molecular dynamic events after excitation of the retinal chromophore into the Franck-Condon state. These early events include a strong electronic polarization, skeletal stretching, and all-trans-to-13-cis isomerization upon formation of the J intermediate. The effectiveness of the photoreaction is ensured by a conical intersection between the electronic excited and ground states, providing highly nonadiabatic coupling to nuclear motions. Here, we study real-time vibrational coherences associated with these motions by analyzing light-induced infrared emission from oriented purple membranes in the 750–1400 cm−1 region. The experimental technique applied is based on second-order femtosecond difference frequency generation on macroscopically ordered samples that also yield information on phase and direction of the underlying motions. Concerted use of several analysis methods resulted in the isolation and characterization of seven different vibrational modes, assigned as C-C stretches, out-of-plane methyl rocks, and hydrogen out-of-plane wags, whereas no in-plane H rock was found. Based on their lifetimes and several other criteria, we deduce that the majority of the observed modes take place on the potential energy surface of the excited electronic state. In particular, the direction sensitivity provides experimental evidence for large intermediate distortions of the retinal plane during the excited-state isomerization process. PMID:21402041

  8. Optimal emission enhancement in orthogonal double-pulse laser-induced breakdown spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Sanginés, R. [Centro de Ciencias Aplicadas y Desarrollo Tecnológico, Universidad Nacional Autónoma de México (CCADET-UNAM), Apartado Postal 70-186, México, DF 04510 (Mexico); Cátedra CONACyT, Centro de Nanociencias y Nanotecnología, Universidad Nacional Autónoma de México, Apartado Postal 14, Ensenada, BC 22800 (Mexico); Contreras, V. [Department of Physics, Tampere University of Technology, P.O. Box 692, FI-33101 Tampere (Finland); Sobral, H., E-mail: martin.sobral@ccadet.unam.mx [Centro de Ciencias Aplicadas y Desarrollo Tecnológico, Universidad Nacional Autónoma de México (CCADET-UNAM), Apartado Postal 70-186, México, DF 04510 (Mexico); Robledo-Martinez, A. [Universidad Autónoma Metropolitana-Unidad Azcapotzalco, Av. San Pablo 180, Azcapotzalco, México, DF 02200 (Mexico)

    2015-08-01

    Orthogonal double-pulse (DP) laser-induced breakdown spectroscopy (LIBS) was performed using reheating and pre-ablative configurations. The ablation pulse power density was varied by two orders of magnitude and the DP experiments were carried out for a wide range of interpulse delays. For both DP-LIBS schemes, the signal enhancement was evaluated with respect to the corresponding single-pulse (SP) LIBS as a function of the interpulse delay. The reheating scheme shows a sharp maximum signal enhancement of up to 200-fold for low ablative power densities (0.4 GW cm{sup −2}); however, for power densities larger than 10 GW cm{sup −2} this configuration did not improve the SP outcome. On the other hand, a more uniform signal enhancement of about 4–6 was obtained for the pre-ablative scheme nearly independently of the used ablative power density. In terms of the signal-to-noise ratio (SNR) the pre-ablative scheme shows a monotonic increment with the ablative power density. Whereas the reheating configuration reaches a maximum at 2.2 GW cm{sup −2}, its enhancement effect collapses markedly for fluencies above 10 GW cm{sup −2}. - Highlights: • Comparison of reheating and pre-ablative double-pulse LIBS was done using a wide range of ablation power densities. • Experimental parameters that could achieve optimal signal-to-noise ratio were investigated. • A reheating scheme is better for low-ablation power densities. • A pre-ablative configuration is better for high-ablation power densities.

  9. X-ray Emission Spectroscopy to Study Ligand Valence Orbitals in Mn Coordination Complexes

    Energy Technology Data Exchange (ETDEWEB)

    Smolentsev, Grigory; Soldatov, Alexander V; Messinger, Johannes; Merz, Kathrin; Weyhermuller, Thomas; Bergmann, Uwe; Pushkar, Yulia; Yano, Junko; Yachandra, Vittal K.; Glatzel, Pieter

    2009-03-02

    We discuss a spectroscopic method to determine the character of chemical bonding and for the identification of metal ligands in coordination and bioinorganic chemistry. It is based on the analysis of satellite lines in X-ray emission spectra that arise from transitions between valence orbitals and the metal ion 1s level (valence-to-core XES). The spectra, in connection with calculations based on density functional theory (DFT), provide information that is complementary to other spectroscopic techniques, in particular X-ray absorption (XANES and EXAFS). The spectral shape is sensitive to protonation of ligands and allows ligands, which differ only slightly in atomic number (e.g., C, N, O...), to be distinguished. A theoretical discussion of the main spectral features is presented in terms of molecular orbitals for a series of Mn model systems: [Mn(H2O)6]2+, [Mn(H2O)5OH]+, [Mn(H2O)5NH2]+, and [Mn(H2O)5NH3]2+. An application of the method, with comparison between theory and experiment, is presented for the solvated Mn2+ ion in water and three Mn coordination complexes, namely [LMn(acac)N3]BPh4, [LMn(B2O3Ph2)(ClO4)], and [LMn(acac)N]BPh4, where L represents 1,4,7-trimethyl-1,4,7-triazacyclononane, acac stands for the 2,4-pentanedionate anion, and B2O3Ph2 represents the 1,3-diphenyl-1,3-dibora-2-oxapropane-1,3-diolato dianion.

  10. Energy level spectroscopy of InSb quantum wells using quantum-well LED emission

    Science.gov (United States)

    Tenev, T. G.; Palyi, A.; Mirza, B. I.; Nash, G. R.; Fearn, M.; Smith, S. J.; Buckle, L.; Emeny, M. T.; Ashley, T.; Jefferson, J. H.; Lambert, C. J.

    2009-02-01

    We have investigated the low-temperature optical properties of InSb quantum-well (QW) light-emitting diodes, with different barrier compositions, as a function of well width. Three devices were studied: QW1 had a 20 nm undoped InSb quantum well with a barrier composition of Al0.143In0.857Sb , QW2 had a 40 nm undoped InSb well with a barrier composition of Al0.077In0.923Sb , and QW3 had a 100 nm undoped InSb well with a barrier composition of Al0.025In0.975Sb . For QW1, the signature of two transitions (CB1-HH1 and CB1-HH2) can be seen in the measured spectrum, whereas for QW2 and QW3 the signature of a large number of transitions is present in the measured spectra. In particular transitions to HH2 can be seen, the first time this has been observed in AlInSb/InSb heterostructures. To identify the transitions that contribute to the measured spectra, the spectra have been simulated using an eight-band k.p calculation of the band structure together with a first-order time-dependent perturbation method (Fermi golden rule) calculation of spectral emittance, taking into account broadening. In general there is good agreement between the measured and simulated spectra. For QW2 we attribute the main peak in the experimental spectrum to the CB2-HH1 transition, which has the highest overall contribution to the emission spectrum of QW2 compared with all the other interband transitions. This transition normally falls into the category of “forbidden transitions,” and in order to understand this behavior we have investigated the momentum matrix elements, which determine the selection rules of the problem.

  11. Dynamics of bolaamphiphilic fluorescent polyenes in lipid bilayers from polarization emission spectroscopy.

    Science.gov (United States)

    Acuña, A Ulises; Amat-Guerri, Francisco; Quesada, Ernesto; Vélez, Marisela

    2006-06-20

    The rotational motions of the biamphiphilic polyenes (bolapolyenes) dimethyl all-(E)-octacosa-10,12,14,16,18-pentaenedioate (DE28:5) and dimethyl all-(E)-tetratriaconta-13,15,17,19,21-pentaenedioate (DE34:5), with head-to-head distances of 34 and 42A, respectively, have been examined by fluorescence anisotropy methods. The membrane-spanning bolapolyenes, which contain a central emitting pentaene group tethered to two methoxycarbonyl opposite polar heads by symmetric C(8) (DE28:5) and C(11) (DE34:5) polymethylene chains, were dispersed in lipid bilayers of DPPC or DMPC, and the stationary and picosecond-resolved emission was recorded as a function of temperature. In fluid-phase DMPC bilayers, three relaxation times could be determined, assigned to fast (0.2 and 2ns) single-bond isomerization processes localized on the alkyl chains, and to whole-molecule oscillations ( approximately 11ns), respectively. The anisotropy decay parameters were further analyzed in terms of a diffusive model for wobbling in a Gaussian ordering potential, to assess the anchoring effect of the symmetric polar heads. In this way, the average rotational diffusion constant of the bolapolyenes, D( perpendicular), could be estimated as 0.022-0.026rad(2) ns(-1) (DMPC bilayers, 35 degrees Celsius), a value that is only 1/3 of that corresponding to the related pentaene fatty acid spanning a single membrane monolayer. In contrast, the amplitude of the equilibrium orientational distribution (theta(half-cone) approximately 50 degrees ) is very similar for both the transmembrane and the single-headed polyenes. The reorientational oscillations of the central emitting group in the bolapolyenes necessarily would produce large-amplitude (2-5A) and very fast (ns) translational motions of the polar heads.

  12. FLASH SPECTROSCOPY: EMISSION LINES FROM THE IONIZED CIRCUMSTELLAR MATERIAL AROUND <10-DAY-OLD TYPE II SUPERNOVAE

    Energy Technology Data Exchange (ETDEWEB)

    Khazov, D.; Yaron, O.; Gal-Yam, A.; Manulis, I.; Rubin, A.; Ofek, E. O.; Horesh, A. [Benoziyo Center for Astrophysics, Faculty of Physics, The Weizmann Institute for Science, Rehovot 76100 (Israel); Kulkarni, S. R.; Kasliwal, M. M.; Cao, Y.; Perley, D. [Astronomy Department, California Institute of Technology, 1200 E. California Boulevard, Pasadena, CA 91125 (United States); Arcavi, I.; Howell, D. A. [Las Cumbres Observatory Global Telescope Network, 6740 Cortona Drive, Suite 102, Goleta, CA 93111 (United States); Sollerman, J. [The Oskar Klein Centre, Department of Astronomy, Stockholm University, AlbaNova, SE-10691 Stockholm (Sweden); Sullivan, M. [School of Physics and Astronomy, University of Southampton, Southampton, SO17 1BJ (United Kingdom); Filippenko, A. V.; Nugent, P. E. [Department of Astronomy, University of California, Berkeley, CA 94720-3411 (United States); Cenko, S. B. [Astrophysics Science Division, NASA Goddard Space Flight Center, Mail Code 661, Greenbelt, MD 20771 (United States); Silverman, J. M. [Department of Astronomy, University of Texas at Austin, Austin, TX 78712 (United States); Ebeling, H. [Institute for Astronomy, University of Hawaii, 2680 Woodlawn Drive, Honolulu, HI 96822 (United States); and others

    2016-02-10

    Supernovae (SNe) embedded in dense circumstellar material (CSM) may show prominent emission lines in their early-time spectra (≤10 days after the explosion), owing to recombination of the CSM ionized by the shock-breakout flash. From such spectra (“flash spectroscopy”), we can measure various physical properties of the CSM, as well as the mass-loss rate of the progenitor during the year prior to its explosion. Searching through the Palomar Transient Factory (PTF and iPTF) SN spectroscopy databases from 2009 through 2014, we found 12 SNe II showing flash-ionized (FI) signatures in their first spectra. All are younger than 10 days. These events constitute 14% of all 84 SNe in our sample having a spectrum within 10 days from explosion, and 18% of SNe II observed at ages <5 days, thereby setting lower limits on the fraction of FI events. We classified as “blue/featureless” (BF) those events having a first spectrum that is similar to that of a blackbody, without any emission or absorption signatures. It is possible that some BF events had FI signatures at an earlier phase than observed, or that they lack dense CSM around the progenitor. Within 2 days after explosion, 8 out of 11 SNe in our sample are either BF events or show FI signatures. Interestingly, we found that 19 out of 21 SNe brighter than an absolute magnitude M{sub R} = −18.2 belong to the FI or BF groups, and that all FI events peaked above M{sub R} = −17.6 mag, significantly brighter than average SNe II.

  13. Improvement of the thermal stability of nickel silicide using a ruthenium interlayer deposited via remote plasma atomic layer deposition

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Inhye [Department of Materials Science and Engineering, Hanyang University, Seoul 04763, South Korea and System LSI Manufacturing Operation Center, Samsung Electronics Co., Ltd, Gyeonggi-do 17113 (Korea, Republic of); Park, Jingyu; Jeon, Heeyoung; Kim, Hyunjung; Shin, Changhee [Department of Nano-scale Semiconductor Engineering, Hanyang University, Seoul 04763 (Korea, Republic of); Shin, Seokyoon; Lee, Kunyoung [Department of Materials Science and Engineering, Hanyang University, Seoul 04763 (Korea, Republic of); Jeon, Hyeongtag, E-mail: hjeon@hanyang.ac.kr [Department of Materials Science and Engineering, Hanyang University, Seoul 04763, South Korea and Department of Nano-scale Semiconductor Engineering, Hanyang University, Seoul 04763 (Korea, Republic of)

    2016-05-15

    In this study, the effects of a thin Ru interlayer on the thermal and morphological stability of NiSi have been investigated. Ru and Ni thin films were deposited sequentially to form a Ni/Ru/Si bilayered structure, without breaking the vacuum, by remote plasma atomic layer deposition (RPALD) on a p-type Si wafer. After annealing at various temperatures, the thermal stabilities of the Ni/Ru/Si and Ni/Si structures were investigated by various analysis techniques. The results showed that the sheet resistance of the Ni/Ru/Si sample was consistently lower compared to the Ni/Si sample over the entire temperature range. Although both samples exhibited the formation of NiSi{sub 2} phases at an annealing temperature of 800 °C, as seen with glancing angle x-ray diffraction, the peaks of the Ni/Ru/Si sample were observed to have much weaker intensities than those obtained for the Ni/Si sample. Moreover, the NiSi film with a Ru interlayer exhibited a better interface and improved surface morphologies compared to the NiSi film without a Ru interlayer. These results show that the phase transformation of NiSi to NiSi{sub 2} was retarded and that the smooth NiSi/Si interface was retained due to the activation energy increment for NiSi{sub 2} nucleation that is caused by adding a Ru interlayer. Hence, it can be said that the Ru interlayer deposited by RPALD can be used to control the phase transformation and physical properties of nickel silicide phases.

  14. Resonant soft X-ray emission spectroscopy of vanadium oxides andrelated compounds

    Energy Technology Data Exchange (ETDEWEB)

    Schmitt, Thorsten

    2004-11-01

    In today's information world, bits of data are processed by semiconductor chips, and stored in the magnetic disk drives. But tomorrow's information technology may see magnetism (spin) and semiconductivity (charge) combined in one ''spintronic'' device that exploits both charge and ''spin'' to carry data (the best of two worlds). Spintronic devices such as spin valve transistors, spin light emitting diodes, non-volatile memory, logic devices, optical isolators and ultra-fast optical switches are some of the areas of interest for introducing the ferromagnetic properties at room temperature in a semiconductor to make it multifunctional. The potential advantages of such spintronic devices will be higher speed, greater efficiency, and better stability at a reduced power consumption. This Thesis contains two main topics: In-depth understanding of magnetism in Mn doped ZnO, and our search and identification of at least six new above room temperature ferromagnetic semiconductors. Both complex doped ZnO based new materials, as well as a number of nonoxides like phosphides, and sulfides suitably doped with Mn or Cu are shown to give rise to ferromagnetism above room temperature. Some of the highlights of this work are discovery of room temperature ferromagnetism in: (1) ZnO:Mn (paper in Nature Materials, Oct issue, 2003); (2) ZnO doped with Cu (containing no magnetic elements in it); (3) GaP doped with Cu (again containing no magnetic elements in it); (4) Enhancement of Magnetization by Cu co-doping in ZnO:Mn; and (5) CdS doped with Mn, and a few others not reported in this thesis. We discuss in detail the first observation of ferromagnetism above room temperature in the form of powder, bulk pellets, in 2-3 {micro}m thick transparent pulsed laser deposited films of the Mn (< 4 at.%) doped ZnO. High-resolution transmission electron microscopy (HRTEM) and electron energy loss spectroscopy (EELS) spectra recorded from 2 to 200nm

  15. Resonant soft X-ray emission spectroscopy of vanadium oxides andrelated compounds

    Energy Technology Data Exchange (ETDEWEB)

    Schmitt, Thorsten [Uppsala Univ. (Sweden)

    2004-01-01

    In today's information world, bits of data are processed by semiconductor chips, and stored in the magnetic disk drives. But tomorrow's information technology may see magnetism (spin) and semiconductivity (charge) combined in one ''spintronic'' device that exploits both charge and ''spin'' to carry data (the best of two worlds). Spintronic devices such as spin valve transistors, spin light emitting diodes, non-volatile memory, logic devices, optical isolators and ultra-fast optical switches are some of the areas of interest for introducing the ferromagnetic properties at room temperature in a semiconductor to make it multifunctional. The potential advantages of such spintronic devices will be higher speed, greater efficiency, and better stability at a reduced power consumption. This Thesis contains two main topics: In-depth understanding of magnetism in Mn doped ZnO, and our search and identification of at least six new above room temperature ferromagnetic semiconductors. Both complex doped ZnO based new materials, as well as a number of nonoxides like phosphides, and sulfides suitably doped with Mn or Cu are shown to give rise to ferromagnetism above room temperature. Some of the highlights of this work are discovery of room temperature ferromagnetism in: (1) ZnO:Mn (paper in Nature Materials, Oct issue, 2003); (2) ZnO doped with Cu (containing no magnetic elements in it); (3) GaP doped with Cu (again containing no magnetic elements in it); (4) Enhancement of Magnetization by Cu co-doping in ZnO:Mn; and (5) CdS doped with Mn, and a few others not reported in this thesis. We discuss in detail the first observation of ferromagnetism above room temperature in the form of powder, bulk pellets, in 2-3 μm thick transparent pulsed laser deposited films of the Mn (< 4 at.%) doped ZnO. High-resolution transmission electron microscopy (HRTEM) and electron energy loss spectroscopy (EELS) spectra recorded from 2 to 200nm

  16. Magnetic Resonance Spectroscopy and Single-Photon Emission Computed Tomography in the Evaluation of Cerebral Tumors: A Case Report

    Science.gov (United States)

    Siasios, Ioannis; Valotassiou, Varvara; Kapsalaki, Eftychia; Tsougos, Ioannis; Georgoulias, Panagiotis; Fotiadou, Aggeliki; Ioannou, Maria; Koukoulis, Georgios; Dimopoulos, Vassilios; Fountas, Kostas

    2017-01-01

    In their daily clinical practice, physicians have to confront diagnostic dilemmas which cannot be resolved by the application of only one imaging technique. In this case report, we present a 66-year-old woman who was admitted to our institution for the surgical resection of a recently diagnosed brain tumor. The patient had a history of epileptic seizures and was hospitalized in the past for anti-phospholipid syndrome related to a non-Hodgkin lymphoma in remission. Magnetic resonance imaging (MRI) examination revealed an enhancing right parasagittal lesion with significant edema suggestive of a high grade glioma. Advanced MRI techniques including proton magnetic resonance spectroscopy (1H-MRS) showed findings compatible of glioma. An additional examination was performed as part of a protocol that we are routinely performing in our institution for all brain tumors including not only the gold standard advanced MRI techniques but also single-photon emission computed tomography (SPECT) with technetium-99m (Tc99m). Brain SPECT indicated the presence of a meningioma which was verified by the histopathology of the resected specimen. In conclusion, a multimodality approach for the pre-surgical assessment of brain tumors has significant advantages not only for the diagnosis but also for the evaluation of intracranial tumors histology. PMID:27924180

  17. Optical emission spectroscopy of deuterium and helium plasma jets emitted from plasma focus discharges at the PF-1000U facility

    Science.gov (United States)

    Skladnik-Sadowska, E.; Dan'ko, S. A.; Kwiatkowski, R.; Sadowski, M. J.; Zaloga, D. R.; Paduch, M.; Zielinska, E.; Kharrasov, A. M.; Krauz, V. I.

    2016-12-01

    Optical emission spectroscopy techniques were used to investigate the spectra of dense deuterium-plasma jets generated by high-current pulse discharges within the large PF-1000U facility and to estimate parameters of plasma inside the jets and their surroundings. Time-resolved optical spectra were recorded by means of a Mechelle®900 spectrometer. From an analysis of the deuterium line broadening, it was estimated that the electron concentration at a distance 57 cm from the electrode outlets amounted to (0.4-3.7) × 1017 cm-3 depending on the initial gas distribution and the time interval of the spectrum registration after the instant of the plasma jet generation. From the re-absorption dip in the Dβ profile, it was assessed that the electron concentration in the surrounding gas was equal to about 1.5 × 1015 cm-3. On the basis of the measured ratio of He II 468.6 nm and He I 587.6 nm line intensities, it was estimated that the electron temperature amounted to about 5.3 eV. Also estimated were some dimensionless parameters of the investigated plasma jets.

  18. 57Fe emission Mössbauer spectroscopy following dilute implantation of 57Mn into In 2O3

    Science.gov (United States)

    Mokhles Gerami, A.; Johnston, K.; Gunnlaugsson, H. P.; Nomura, K.; Mantovan, R.; Masenda, H.; Matveyev, Y. A.; Mølholt, T. E.; Ncube, M.; Shayestehaminzadeh, S.; Unzueta, I.; Gislason, H. P.; Krastev, P. B.; Langouche, G.; Naidoo, D.; Ólafsson, S.

    2016-12-01

    Emission Mössbauer spectroscopy has been utilised to characterize dilute 57Fe impurities in In 2O3 following implantation of 57Mn ( T 1/2 = 1.5 min.) at the ISOLDE facility at CERN. From stoichiometry considerations, one would expect Fe to adopt the valence state 3 + , substituting In 3+, however the spectra are dominated by spectral lines due to paramagnetic Fe2+. Using first principle calculations in the framework of density functional theory (DFT), the density of states of dilute Fe and the hyperfine parameters have been determined. The hybridization between the 3d-band of Fe and the 2p band of oxygen induces a spin-polarized hole on the O site close to the Fe site, which is found to be the cause of the Fe2+ state in In 2O3. Comparison of experimental data to calculated hyperfine parameters suggests that Fe predominantly enters the 8b site rather than the 24d site of the cation site in the Bixbyite structure of In 2O3. A gradual transition from an amorphous to a crystalline state is observed with increasing implantation/annealing temperature.

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

    Science.gov (United States)

    Ivanjek, L.; Shaffer, P. S.; McDermott, L. C.; Planinic, M.; Veza, D.

    2015-02-01

    This is the second of two closely related articles (Paper I and Paper II) that together illustrate how research in physics education has helped guide the design of instruction that has proved effective in improving student understanding of atomic spectroscopy. Most of the more than 1000 students who participated in this four-year investigation were science majors enrolled in the introductory calculus-based physics course at the University of Washington (UW) in Seattle, WA, USA. The others included graduate and undergraduate teaching assistants at UW and physics majors in introductory and advanced physics courses at the University of Zagreb, Zagreb, Croatia. About half of the latter group were preservice high school physics teachers. Paper I describes how several conceptual and reasoning difficulties were identified among university students as they tried to relate a discrete line spectrum to the energy levels of atoms in a light source. This second article (Paper II) illustrates how findings from this research informed the development of a tutorial that led to improvement in student understanding of atomic emission spectra.

  20. Characterization of low temperature graphene synthesis in inductively coupled plasma chemical vapor deposition process with optical emission spectroscopy.

    Science.gov (United States)

    Ma, Yifei; Kim, Daekyoung; Jang, Haegyu; Cho, Sung Min; Chae, Heeyeop

    2014-12-01

    Low-temperature graphene was synthesized at 400 degrees C with inductively coupled plasma chemical vapor deposition (PECVD) process. The effects of plasma power and flow rate of various carbon containing precursors and hydrogen on graphene properties were investigated with optical emission spectroscopy (OES). Various radicals monitored by OES were correlated with graphene film properties such as sheet resistance, I(D)/I(G) ratio of Raman spectra and transparency. C2H2 was used as a main precursor and the increase of plasma power enhanced intensity of carbon (C2) radical OES intensity in plasma, reduced sheet resistance and increased transparency of graphene films. The reduced flow rate of C2H2 decreased sheet resistance and increased transparency of graphene films in the range of this study. H2 addition was found to increase sheet resistance, transparency and attributed to reduction of graphene grain and etching graphene layers. OES analysis showed that C2 radicals contribute to graphite networking and sheet resistance reduction. TEM and AFM were applied to provide credible information that graphene had been successfully grown at low temperature.

  1. Spectroscopy of superluminous supernova host galaxies. A preference of hydrogen-poor events for extreme emission line galaxies

    CERN Document Server

    Leloudas, G; Kruehler, T; Gorosabel, J; Christensen, L; Mehner, A; Postigo, A de Ugarte; Amorin, R; Thoene, C C; Anderson, J P; Bauer, F E; Gallazzi, A; Helminiak, K G; Hjorth, J; Ibar, E; Malesani, D; Morell, N; Vinko, J; Wheeler, J C

    2014-01-01

    Superluminous supernovae (SLSNe) were only discovered recently due to their preference for occurring in faint dwarf galaxies. Understanding why stellar evolution yields different types of stellar explosions in these environments is fundamental in order to both uncover the elusive progenitors of SLSNe and to study star formation in dwarf galaxies. In this paper, we present the first results of our project to study SUperluminous Supernova Host galaxIES (SUSHIES), focusing on the sample for which we have obtained spectroscopy. We show that SLSNe-I and SLSNe-R (hydrogen-poor) often (~50% in our sample) occur in a class of galaxies that is known as Extreme Emission Line Galaxies (EELGs). The probability of this happening by chance is negligible and we therefore conclude that the extreme environmental conditions and the SLSN phenomenon are related. In contrast, SLSNe-II (hydrogen-rich) occur in more massive, more metal-rich galaxies with softer radiation fields. Therefore, if SLSNe-II constitute a uniform class, th...

  2. Determination of plasma trace elements in tumor-bearing animals by proton-induced X-ray emission spectroscopy.

    Science.gov (United States)

    Fogle, M; Daly, B; Evans, M; Justiniano, E L; Kovacs, C J; Shinpaugh, J L; Toburen, L H

    2001-11-01

    Although altered levels of circulating essential trace elements are known to accompany malignant disease, the lack of sensitivity of conventional detection methods has generally limited their study to clinical conditions involving extensive disease (i.e., significant tumor burden). As such, the application of altered trace element levels as potential prognostic guides or as response indicators subsequent to treatment has been of limited use. During this study, proton-induced X-ray emission spectroscopy was evaluated as a tool to determine trace element imbalances in a murine tumor model. Using plasma from C57B1/6 mice bearing the syngeneic Lewis lung carcinoma (LLCa), levels of Fe, Cu, and Zn, as well as changes in the Cu /Zn ratio, were measured in animals carrying an increasing primary tumor burden. The plasma levels of Fe, Cu, and Zn were found to decrease significantly 7 d following implants of LLCa cells with no significant change observed in the Cu/Zn ratio. By d 21, however, an increase in the Cu/Zn ratio was found to accompany increased growth of the LLCa tumor; the plasma levels of Cu had returned to normal levels, whereas both the Fe and Zn plasma levels remained lowered. Collectively, the results suggest that although a net change in individual plasma trace element concentrations might not be accurately associated with tumor growth, a clear relationship was established between the Cu/Zn ratio and tumor size.

  3. Optical emission spectroscopy of OH lines in N2 and Ar plasma during the treatments of cotton fabric

    Science.gov (United States)

    Skoro, Nikola; Puac, Nevena; Spasic, Kosta; Malovic, Gordana; Gorjanc, Marija; Petrovic, Zoran Lj

    2016-09-01

    Low pressure non-equilibrium plasmas are proven to be irreplaceable tool in material processing. Among other fields their applications in treatments of textiles are still diversifying, but the main role of plasma is activation of the surface of treated sample. After, or during, the treatments these surfaces can be covered with different materials or species (such as microcapsules) that enhance properties of the fabric. In order to investigate mechanisms how active species from plasma interact with the cotton surface, we studied both plasma and surface properties. Bleached cotton samples were treated in low-pressure nitrogen and argon plasma in a chamber with parallel-plate electrodes. The effect of the plasma treatment on the cotton samples was investigated with the colorimetric measurements on dyes absorption by a spectrophotometer. Optical emission spectroscopy was performed by using spectrometer with a sensitive CCD camera. We have recorded the evolution of the maximum of the intensity of OH and N2 second positive band lines. Measurement were done with and without samples in the chamber and comparison between the lines intensity was made. The parameters for optimal plasma treatment conditions were determined. Research supported by the MESTD, projects III41011 and ON171037.

  4. A combined FTIR and infrared emission spectroscopy investigation of layered double hydroxide as an effective electron donor

    Science.gov (United States)

    Zhang, Jia; Wei, Feng; Liang, Ying; Zhou, Jizhi; Xi, Yunfei; Qian, Guangren; Frost, Ray

    2016-02-01

    A novel method has been presented to characterize electron transfer in layered double hydroxides (LDHs) utilizing an investigation combing FTIR and infrared emission spectroscopy. At room temperature, electron could transfer to interlayer Fe3 + through monodentate ligand cyanide, and resulted in a reduction of 40% Fe3 + to Fe2 +. When the environmental temperature increased from 25 to 300 °C, reduction of Fe3 + and Ni2 + increased to 94% and 42%. Furthermore, electron also transferred to interlayer cation through multidentate ligand EDTA. As a result, LDHs has been proven to be an effective electron donor, and FTIR was a feasible tool in characterizing this property by monitoring the valence state of cations. It was also concluded that octahedral units with OH- groups in LDH layer functioned as electron donor centers. Driving force for electron transfer is attributed to the charge density difference between cation layer and probe anion. These results could help to explain the mechanism of various applications of LDHs in catalysis and photocatalysis.

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

    Science.gov (United States)

    Ivanjek, L.; Shaffer, P. S.; McDermott, L. C.; Planinic, M.; Veza, D.

    2015-01-01

    This is the first of two closely related articles (Paper I and Paper II) that together illustrate how research in physics education has helped guide the design of instruction that has proved effective in improving student understanding of atomic spectroscopy. Most of the more than 1000 students who participated in this four-year investigation were science majors enrolled in the introductory calculus-based physics course at the University of Washington (UW) in Seattle, WA, USA. The others included graduate and undergraduate teaching assistants at UW and physics majors in introductory and advanced physics courses at the University of Zagreb, Zagreb, Croatia. About half of the latter group were preservice high school physics teachers. This article (Paper I) describes how several serious conceptual and reasoning difficulties were identified among students as they tried to relate a discrete line spectrum to the energy levels of atoms in a light source. Paper II illustrates how findings from this research informed the development of a tutorial that led to significant improvement in student understanding of atomic emission spectra.

  6. Diagnosis of Methane Plasma Generated in an Atmospheric Pressure DBD Micro-Jet by Optical Emission Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    ZHANG Jun-Feng; BIAN Xin-Chao; CHEN Qiang; LIU Fu-Ping; LIU Zhong-Wei

    2009-01-01

    Diagnosis of methane plasma,generated in an atmospheric pressure dielectric barrier discharge (DBD) microplasma jet with a quartz tube as dielectric material by a 25 kHz sinusoidal ac power source,is conducted by optical emission spectroscopy (OES).The reactive radicals in methane plasma such as CH,C2,and Ha are detected insitu by OES.The possible dissociation mechanism of methane in diluted Ar plasma is deduced from spectra.In addition,the density of CH radical,which is considered as one of the precursors in diamond-like (DLC) film formation,affected by the parameters of input voltage and the feed gas flow rate,is emphasized. With the Boltzmann plots,four Ar atomic spectral lines (located at 675.28nm,687.13nm,738.40nm and 794.82nm,respectively) are chosen to calculate the electron temperature,and the dependence of electron temperature on discharge parameters is also investigated.

  7. Insufficiency of Positron Emission Tomography and Magnetic Resonance Spectroscopy in the Diagnosis of Intravascular Lymphoma of the Central Nervous System

    Directory of Open Access Journals (Sweden)

    Nobuyuki Kawai

    2012-07-01

    Full Text Available Intravascular large B-cell lymphoma (IVL is a rare type of extranodal lymphoma with an aggressive clinical course characterized by the proliferation of lymphoma cells within the lumen of small vessels. Diagnosis is often difficult because of marked variability in clinical presentation and nonspecific laboratory and radiological findings, especially when central nervous system (CNS symptoms are the only manifestation. Modern metabolic imaging techniques such as positron emission tomography (PET and 1H-magnetic resonance spectroscopy (MRS have been reported to be useful in the diagnosis of conventional primary CNS lymphoma. We report the case of a 69-year-old man who presented with a progressive leukoencephalopathic syndrome. The patient was examined by 18F-fluorodeoxyglucose and 11C-methionine PET and MRS, but none of these examinations were able to show the presence of a tumor in the lesions or to clarify the tumor characteristics. Brain biopsy was the only way to obtain a definite diagnosis of IVL. The patient was treated intensively with standard immunochemotherapy but died 6 months after the diagnosis. Here, we discuss the insufficiency of modern metabolic imaging techniques, including PET and MRS, and recommend a rapid decision of brain biopsy in the diagnosis of IVL only involving the CNS.

  8. Physical properties of emission-line galaxies at z ∼ 2 from near-infrared spectroscopy with Magellan fire

    Energy Technology Data Exchange (ETDEWEB)

    Masters, Daniel; Siana, Brian; Mobasher, Bahram; Domínguez, Alberto [Department of Physics and Astronomy, University of California, Riverside, CA 92521 (United States); McCarthy, Patrick; Blanc, Guillermo; Dressler, Alan [Carnegie Observatories, Pasadena, CA 91101 (United States); Malkan, Mathew; Ross, Nathaniel R. [Department of Physics and Astronomy, UCLA, Los Angeles, CA 90095 (United States); Atek, Hakim [Laboratoire d' Astrophysique Ecole Polytechnique Fédérale, CH-1290 Sauverny (Switzerland); Henry, Alaina [Astrophysics Science Division, Goddard Space Flight Center, Greenbelt, MD 20771 (United States); Martin, Crystal L. [Department of Physics, Universitey of California, Santa Barbara, CA 93106 (United States); Rafelski, Marc; Colbert, James [Spitzer Science Center, California Institute of Technology, Pasadena, CA 91125 (United States); Hathi, Nimish P. [Aix Marseille Université, CNRS, LAM (Laboratoire d' Astrophysique de Marseille) UMR 7326, F-13388 Marseille (France); Scarlata, Claudia [Minnesota Institute for Astrophysics, University of Minnesota, Minneapolis, MN 55455 (United States); Bunker, Andrew J. [Department of Physics, University of Oxford (United Kingdom); Bedregal, Alejandro G. [Department of Physics and Astronomy, Tufts University, Medford, MA 02155 (United States); Teplitz, Harry [Infrared Processing and Analysis Center, Caltech, Pasadena, CA 91125 (United States)

    2014-04-20

    We present results from near-infrared spectroscopy of 26 emission-line galaxies at z ∼ 2.2 and z ∼ 1.5 obtained with the Folded-port InfraRed Echellette (FIRE) spectrometer on the 6.5 m Magellan Baade telescope. The sample was selected from the WFC3 Infrared Spectroscopic Parallels survey, which uses the near-infrared grism of the Hubble Space Telescope Wide Field Camera 3 (WFC3) to detect emission-line galaxies over 0.3 ≲ z ≲ 2.3. Our FIRE follow-up spectroscopy (R ∼ 5000) over 1.0-2.5 μm permits detailed measurements of the physical properties of the z ∼ 2 emission-line galaxies. Dust-corrected star formation rates for the sample range from ∼5-100 M {sub ☉} yr{sup –1} with a mean of 29 M {sub ☉} yr{sup –1}. We derive a median metallicity for the sample of 12 + log(O/H) = 8.34 or ∼0.45 Z {sub ☉}. The estimated stellar masses range from ∼10{sup 8.5}-10{sup 9.5} M {sub ☉}, and a clear positive correlation between metallicity and stellar mass is observed. The average ionization parameter measured for the sample, log U ≈ –2.5, is significantly higher than what is found for most star-forming galaxies in the local universe, but similar to the values found for other star-forming galaxies at high redshift. We derive composite spectra from the FIRE sample, from which we measure typical nebular electron densities of ∼100-400 cm{sup –3}. Based on the location of the galaxies and composite spectra on diagnostic diagrams, we do not find evidence for significant active galactic nucleus activity in the sample. Most of the galaxies, as well as the composites, are offset diagram toward higher [O III]/Hβ at a given [N II]/Hα, in agreement with other observations of z ≳ 1 star-forming galaxies, but composite spectra derived from the sample do not show an appreciable offset from the local star-forming sequence on the [O III]/Hβ versus [S II]/Hα diagram. We infer a high nitrogen-to-oxygen abundance ratio from the composite spectrum, which

  9. THE SMARTS MULTI-EPOCH OPTICAL SPECTROSCOPY ATLAS (SaMOSA): AN ANALYSIS OF EMISSION LINE VARIABILITY IN SOUTHERN HEMISPHERE FERMI BLAZARS

    Energy Technology Data Exchange (ETDEWEB)

    Isler, Jedidah C. [Chancellor’s Faculty Fellow, Syracuse University, Department of Physics, Syracuse, NY 13244 (United States); Urry, C. M.; Bailyn, C.; Coppi, P.; Brady, M.; MacPherson, E.; Hasan, I.; Buxton, M. [Department of Astronomy, Yale University, P.O. Box 208101, New Haven, CT 06520-8101 (United States); Smith, P. S., E-mail: jcisler@syr.edu [Steward Observatory, University of Arizona, 933 N. Cherry Avenue, Tuscon, AZ 85721 (United States)

    2015-05-01

    We present multi-epoch optical spectroscopy of seven southern Fermi-monitored blazars from 2008 to 2013 using the Small and Medium Aperture Research Telescope System (SMARTS), with supplemental spectroscopy and polarization data from the Steward Observatory. We find that the emission lines are much less variable than the continuum; four of seven blazars had no detectable emission line variability over the 5 yr observation period. This is consistent with photoionization primarily by an accretion disk, allowing us to use the lines as a probe of disk activity. Comparing optical emission line flux with Fermi γ-ray flux and optical polarized flux, we investigate whether relativistic jet variability is related to the accretion flow. In general, we see no such dependence, suggesting that the jet variability is likely caused by internal processes like turbulence or shock acceleration rather than a variable accretion rate. However, three sources showed statistically significant emission line flares in close temporal proximity to very large Fermi γ-ray flares. While we do not have sufficient emission line data to quantitatively assess their correlation with the γ-ray flux, it appears that in some cases the jet might provide additional photoionizing flux to the broad-line region (BLR), which implies that some γ-rays are produced within the BLR, at least for these large flares.

  10. GRB hosts through cosmic time. VLT/X-Shooter emission-line spectroscopy of 96 γ-ray-burst-selected galaxies at 0.1

    NARCIS (Netherlands)

    T. Krühler; D. Malesani; J.P.U. Fynbo; O.E. Hartoog; J. Hjorth; P. Jakobsson; D.A. Perley; A.. Rossi; P. Schady; S. Schulze; N.R. Tanvir; S.D. Vergani; K. Wiersema; P.M.J. Afonso; J. Bolmer; Z. Cano; S. Covino; V. D’Elia; A. de Ugarte Postigo; R. Filgas; M. Friis; J.F. Graham; J. Greiner; P. Goldoni; A. Gomboc; F. Hammer; J. Japelj; D.A. Kann; L. Kaper; S. Klose; A.J. Levan; G. Leloudas; B. Milvang-Jensen; A. Nicuesa Guelbenzu; E. Palazzi; E. Pian; S. Piranomonte; R. Sánchez-Ramírez; S. Savaglio; J. Selsing; G. Tagliaferri; P.M. Vreeswijk; D.J. Watson; D. Xu

    2015-01-01

    We present data and initial results from VLT/X-Shooter emission-line spectroscopy of 96 galaxies selected by long γ-ray bursts (GRBs) at 0.1

  11. VERITAS (Venus Emissivity, Radio Science, InSAR, Topo-graphy And Spectroscopy): A Proposed Discovery Mission

    Science.gov (United States)

    Smrekar, Suzanne; Dyar, Melinda; Hensley, Scott; Helbert, Joern; VERITAS Science Team

    2016-10-01

    VERITAS addresses one of the most fundamental questions in planetary evolution: How Earth-like is Venus? These twin planets diverged down different evolutionary paths, yet Venus may hold lessons for past and future Earth, as well as for Earth-sized exoplanets. VERITAS will search for the mineralogical fingerprints of past water, follow up on the discoveries of recent volcanism and the possible young surface age, and reveal the conditions that have prevented plate tectonics from developing. Collectively these questions address how Venus ended up a sulfurous inferno while Earth became habitable.VERITAS carries the Venus Interferometric Synthetic Aperture Radar (VISAR) and the Venus Emissivity Mapper (VEM), plus a gravity science investigation.The VISAR X-band radar produces: 1) a global digital elevation model (DEM) with 250 m postings, 5 m height accuracy, 2) Synthetic aperture radar (SAR) global imaging with 30 m pixels, 3) SAR imaging at 15 m for targeted areas, and 4) surface deformation from repeat pass interferometry (RPI) at 2 mm height precision for targeted, potentially active areas. VEM [see Helbert abstract] will measure surface emissivity, look for active volcanic flows and outgassing of water over ~78% of the surface using 6 NIR surface bands within 5 atmospheric windows and 8 bands for calibration of clouds, stray light, and water vapor.VERITAS uses Ka-band uplink and downlink to create a global gravity field with 3 mgal accuracy and 145 km resolution (130 spherical harmonic degree and order or d&o) and providing a significantly higher resolution field with much more uniform resolution than that available from Magellan.VERITAS will create a rich data set of high resolution topography, imaging, spectroscopy, and gravity. These co-registered data sets will be on par with those acquired for Mercury, Mars and the Moon that have revolutionized our understanding of these bodies. VERITAS would be a valuable asset for future lander or probe missions, collecting

  12. Evaluation of lithium determination in three analyzers: flame emission, flame atomic absorption spectroscopy and ion selective electrode

    Directory of Open Access Journals (Sweden)

    Mehri Aliasgharpour

    2009-10-01

    Full Text Available Background: Lithium carbonate salt has become an increasingly important substance in the treatment of manic depressive disorders, and its relatively narrow therapeutic range has caused laboratories to monitor the serum concentration carefully. In the present work we evaluated lithium measurement in 3 different analyzers. Methods & Materials: Three different analyzers including Flame Emission (FES, Flame Atomic Absorption Spectroscopy (FAAS, and Ion Selective Electrode (ISE were used. All chemicals had a grade suitable for trace metal analysis. Results: Within-day precision of CV was ≤ 1.5% for FES & FAAS, except for ISE (1.9% CV. Between-days precision of CV was less for FES than for FAAS and ISE (1.3% versus 2.2% & 2.3%. The percent recovery of added lithium in pooled patients’ serum was higher for ISE than for FASS and FES (103.4% versus 96.2% and 94.6%. We also obtained a higher average lithium concentration for patients’ serum samples (n=16 measured by ISE than for FAAS and FES (0.825±0.30 versus 0.704±0.26 & 0.735±0.19. Paired t-test results revealed a significant difference (p< 0.001 for patient sera analyzed with FAAS and ISE. Conclusion: We report higher results for ISE than the other two analyzers and conclude that the choice between the two flame methods for patients’ serum lithium determination is arbitrary and that FES analyzer is a more attractive routine alternative for lithium determination than FAAS because of its cost and ease of performance. In addition, the results obtained by ISE are precise. However, its accuracy may depend on other interfering factors.

  13. Atomic emission spectroscopy

    Science.gov (United States)

    Andrew, K. H.

    1975-01-01

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

  14. Issues in deep ocean collinear double-pulse laser induced breakdown spectroscopy: Dependence of emission intensity and inter-pulse delay on solution pressure

    Energy Technology Data Exchange (ETDEWEB)

    Lawrence-Snyder, Marion; Scaffidi, Jonathan P.; Pearman, William F.; Gordon, Christopher M.; Angel, S. Michael

    2014-09-01

    Double-pulse laser-induced breakdown spectroscopy (DP-LIBS) with a collinear laser beam orientation is shown for high-pressure bulk aqueous solutions (up to 50 bar) along with bubble and plasma images. These investigations reveal that the emission plasma is quenched much more rapidly in solution requiring much shorter detector gate delays than for typical LIBS measurements in air. Also, the emission is inversely proportional to solution pressure, and the most intense emission at all pressures occurs when the laser-induced vapor bubble is at a maximum diameter. It is also shown that the laser-induced bubble grows initially at the same rate for all solution pressures, collapsing more quickly as the pressure is increased. Intense emission is best obtained for conditions where the laser-induced bubble formed by the first laser pulse is small and spherically shaped. - Highlights: • Collinear double-pulse LIBS is shown for 50 bar bulk aqueous solutions. • LIBS plasma in solution is much more rapidly quenched than a LIBS plasma in air. • For DP LIBS, the emission is inversely proportional to solution pressure. • Laser-induced bubble growth rate is the same at all solution pressures. • Large spherical laser-induced bubbles produce the strongest DP LIBS emission.

  15. Qualitative tissue differentiation by analysing the intensity ratios of atomic emission lines using laser induced breakdown spectroscopy (LIBS): prospects for a feedback mechanism for surgical laser systems.

    Science.gov (United States)

    Kanawade, Rajesh; Mahari, Fanuel; Klämpfl, Florian; Rohde, Maximilian; Knipfer, Christian; Tangermann-Gerk, Katja; Adler, Werner; Schmidt, Michael; Stelzle, Florian

    2015-01-01

    The research work presented in this paper focuses on qualitative tissue differentiation by monitoring the intensity ratios of atomic emissions using 'Laser Induced Breakdown Spectroscopy' (LIBS) on the plasma plume created during laser tissue ablation. The background of this study is to establish a real time feedback control mechanism for clinical laser surgery systems during the laser ablation process. Ex-vivo domestic pig tissue samples (muscle, fat, nerve and skin) were used in this experiment. Atomic emission intensity ratios were analyzed to find a characteristic spectral line for each tissue. The results showed characteristic elemental emission intensity ratios for the respective tissues. The spectral lines and intensity ratios of these specific elements varied among the different tissue types. The main goal of this study is to qualitatively and precisely identify different tissue types for tissue specific laser surgery. © 2015 The Authors. Journal of Biophotonics published by WILEY-VCH Verlag.

  16. No Thermal Inversion and a Solar Water Abundance for the Hot Jupiter HD209458b from HST WFC3 Emission Spectroscopy

    CERN Document Server

    Line, Michael R; Bean, Jacob; Desert, Jean-Michel; Fortney, Jonathan J; Kreidberg, Laura; Madhusudhan, Nikku; Showman, Adam P; Diamond-Lowe, Hannah

    2016-01-01

    The nature of the vertical thermal structure of hot Jupiter atmospheres is one of the key questions raised by the characterization of transiting exoplanets over the last decade. There have been claims that many hot Jupiter's exhibit vertical profiles with increasing temperature with decreasing pressure in the infrared photosphere that leads to the reversal of molecular absorption bands into emission features (an inversion). However, these claims have been based on broadband photometry rather than the unambiguous identification of emission features with spectroscopy, and the chemical species that could cause the thermal inversions by absorbing stellar irradiation at high altitudes have not been identified despite extensive theoretical and observational effort. Here we present high precision HST WFC3 observations of the dayside emission spectrum of the hot Jupiter HD209458b; the first exoplanet suggested to have a thermal inversion. Our observations resolve a water band in absorption at 6.2 sigma confidence. Wh...

  17. Volcanic SO2 and SiF4 visualization using 2-D thermal emission spectroscopy – Part 1: Slant-columns and their ratios

    Directory of Open Access Journals (Sweden)

    M. Grutter

    2012-02-01

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

  18. Volcanic SO2 and SiF4 visualization using 2-D thermal emission spectroscopy - Part 1: Slant-columns and their ratios

    Science.gov (United States)

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

    2012-02-01

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

  19. Characterization of metallic nanoparticles by high-resolution X-ray absorption and X-ray emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kuehn, Timna-Josua

    2012-03-15

    In almost all areas of technology, metallic nanoparticles are of interest due to their special thermal, electronic, magnetic and optical properties. Their special properties are mainly due to their small size which implies the relevance of quantum effects as well as the significance of the surface: For 2 nm nanoparticles, the surface-to-volume ratio is already 1:1. However, the identification of surface-to-volume interactions - that are responsible for the new properties - is a difficult task due to the small size that inhibits a lot of 'standard' techniques to be applicable. Here X-ray absorption/emission spectroscopy (XAS/XES) is a favorable tool for the characterization of nanoparticles, independent on size, degree of crystallinity and shape/condition of the surface. Using XAS, a tempered nanosized Co{sub 3}Pt/C catalyst have been investigated. Its outstanding oxygen-reduction reaction (ORR) properties in a fuel cell could be related to a lowered Pt 5d-band center connected to a tightened Pt-Pt bonding distance, leading to a weakening of the oxygen adsorption strength so that the ORR may proceed faster. One drawback remains, however, as the properties found by (standard) XAS are summed up for different chemical environments of the chosen element. Thus, no distinction can be made between, e.g., the pure metal in a nanoparticles' interior and the ligated metal in the outer shells or surface. Here, high-resolution fluorescence-detected XAS (HRFD-XAS) provides additional opportunities as, due to its chemical sensitivity, it leads to site-selective XAS. For a system of 6 nm sized Co nanoparticles, build up of a metallic core surrounded by a protecting shell, that resulted from the 'smooth oxidation' process, this technique of site-selective XAS was proven to be applicable. For the first time, the interior and outer shell of a metallic nanoparticle could be characterized separately. In particular, the Co-hcp phase could be determined for the

  20. The Grism Lens-Amplified Survey from Space (GLASS). III. A census of Ly\\alpha\\ Emission at $z\\gtrsim$7 from HST Spectroscopy

    CERN Document Server

    Schmidt, K B; Bradač, M; Vulcani, B; Huang, K -H; Hoag, A; Maseda, M; Guaita, L; Pentericci, L; Brammer, G B; Dijkstra, M; Dressler, A; Fontana, A; Henry, A L; Jones, T A; Mason, C; Trenti, M; Wang, X

    2015-01-01

    [abbreviated] We present a census of Ly\\alpha\\ emission at $z\\gtrsim7$ utilizing deep near infrared HST grism spectroscopy from the first six completed clusters of the Grism Lens-Amplified Survey from Space (GLASS). In 24/159 photometrically selected galaxies we detect emission lines consistent with Ly\\alpha\\ in the GLASS spectra. Based on the distribution of signal-to-noise ratios and on simulations we expect the completeness and the purity of the sample to be 40-100% and 60-90%, respectively. For the objects without detected emission lines we show that the observed (not corrected for lensing magnification) 1$\\sigma$ flux limits reaches $5\\times10^{-18}$erg/s/cm$^{2}$ per position angle over the full wavelength range of GLASS (0.8-1.7$\\mu$m). Based on the conditional probability of Ly\\alpha\\ emission measured from the ground at $z\\sim7$ we would have expected 12-18 Ly\\alpha\\ emitters. This is consistent with the number of detections, within the uncertainties, confirming the drop in Ly\\alpha\\ emission with re...

  1. VLT/XSHOOTER & Subaru/MOIRCS Spectroscopy of HUDF-YD3: No Evidence for Lyman-alpha Emission at z=8.55

    CERN Document Server

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

    2013-01-01

    We present spectroscopic observations with VLT/XSHOOTER and Subaru/MOIRCS of a relatively bright Y-band drop-out galaxy in the Hubble Ultra Deep Field, first selected by Bunker et al. (2010), McLure et al. (2010) and Bouwens et al. (2010) to be a likely z~8-9 galaxy on the basis of its colours in the HST ACS and WFC3 images. This galaxy, HUDF.YD3 (also known as UDFy-38135539) has been targetted for VLT/SINFONI integral field spectroscopy by Lehnert et al. (2010), who published a candidate Lyman-alpha emission line at z=8.55 from this source. In our independent spectroscopy using two different infrared spectrographs (5 hours with VLT/XSHOOTER and 11 hours with Subaru/MOIRCS) we are unable to reproduce this line. We do not detect any emission line at the spectral and spatial location reported in Lehnert et al. (2010), despite the expected signal in our combined MOIRCS & XSHOOTER data being 5-sigma. The line emission also seems to be ruled out by the faintness of this object in recently extremely deep F105W ...

  2. Soft X-ray emission spectroscopy used for the characterization of a-C and CN{sub x} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Nepijko, S.A., E-mail: nepijko@uni-mainz.de [Institute of Physics, University of Mainz, Staudingerweg 7, 55128 Mainz (Germany); Chernenkaya, A. [Institute of Physics, University of Mainz, Staudingerweg 7, 55128 Mainz (Germany); Graduate School Materials Science in Mainz, Staudingerweg 9, 55128 Mainz (Germany); Medjanik, K.; Chernov, S.V. [Institute of Physics, University of Mainz, Staudingerweg 7, 55128 Mainz (Germany); Klimenkov, M. [Institute for Applied Materials, Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Vlasenko, O.V. [Sumy State University, Rimsky-Korsakov str. 2, 40007 Sumy (Ukraine); Petrovskaya, S.S. [Frantsevich Institute for Problems of Materials Science, National Academy of Sciences of Ukraine, Krzhizhanovsky str. 3, 03142 Kiev (Ukraine); Odnodvorets, L.V. [Sumy State University, Rimsky-Korsakov str. 2, 40007 Sumy (Ukraine); Zaulichnyy, Ya.V. [National Technical University of Ukraine (KPI), Pobedy Av. 37, 03056 Kiev (Ukraine); Schönhense, G. [Institute of Physics, University of Mainz, Staudingerweg 7, 55128 Mainz (Germany)

    2015-02-27

    We present the results of a soft X-ray emission spectroscopy study of a-C and CN{sub x} films on a Si(100) substrate. Also for the characterization of the homogeneity in depth of these films electron energy loss spectroscopy measurements with localization better than 4 nm were carried out. In case of CN{sub x} films the highest diamond-like modification occurs in the region close to the Si(100) substrate. The film density decreases with increasing distance from the substrate and becomes almost constant in range of thicknesses more than ~ 2 nm. - Highlights: • CN{sub x} and a-C film densities decrease with the increase of thickness. • Density increases with the decrease of Si(100) substrate temperature at preparation. • Highest concentration of the diamond-like structure is in the substrate vicinity. • It reduces further from the substrate and stabilizes at thickness ≥ 2 nm.

  3. ESTIMATION OF METHANE EMISSIONS FROM A SURFACE COAL MINE USING OPEN-PATH FTIR SPECTROSCOPY AND MODELING TECHNIQUES

    Science.gov (United States)

    A new measurements methodology has been developed which allows the rapid and efficient measurement of methane (CH4) emissions from surface coal mines. An initial field trial of this methodology has been completed, and results from the field trial revealed that emissions from one ...

  4. Noninvasive express diagnostics of pulmonary diseases based on control of patient's gas emission using methods of IR and terahertz laser spectroscopy

    Science.gov (United States)

    Starikova, M. K.; Bulanova, A. A.; Bukreeva, E. B.; Karapuzikov, A. A.; Karapuzikov, A. I.; Kistenev, Y. V.; Klementyev, V. M.; Kolker, D. B.; Kuzmin, D. A.; Nikiforova, O. Y.; Ponomarev, Yu. N.; Sherstov, I. V.; Boyko, A. A.

    2013-11-01

    Pulmonary diseases diagnostics always occupies one of the key positions in medicine practices. A large variety of high technology methods are used today, but none of them cannot be used for early screening of pulmonary diseases. We discuss abilities of methods of IR and terahertz laser spectroscopy for noninvasive express diagnostics of pulmonary diseases on a base of analysis of absorption spectra of patient's gas emission, in particular, exhaled air. Experience in the field of approaches to experimental data analysis and hard-ware realization of gas analyzers for medical applications is also discussed.

  5. Infrared heterodyne spectroscopy of astronomical and laboratory sources at 8.5 micron. [absorption line profiles of nitrogen oxide and black body emission from Moon and Mars

    Science.gov (United States)

    Mumma, M.; Kostiuk, T.; Cohen, S.; Buhl, D.; Vonthuna, P. C.

    1974-01-01

    The first infrared heterodyne spectrometer using tuneable semiconductor (PbSe) diode lasers has been constructed and was used near 8.5 micron to measure absorption line profiles of N2O in the laboratory and black body emission from the Moon and from Mars. Spectral information was recorded over a 200 MHz bandwidth using an 8-channel filter bank. The resolution was 25 MHz and the minimum detectable (black body) power was 1 x 10 to the minus 16th power watts for 8 minutes of integration. The results demonstrate the usefulness of heterodyne spectroscopy for the study of remote and local sources in the infrared.

  6. Simulating Valence-to-Core X-ray Emission Spectroscopy of Transition Metal Complexes with Time-Dependent Density Functional Theory

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yu; Mukamel, Shaul; Khalil, Munira; Govind, Niranjan

    2015-11-09

    Valence-to-core (VtC) X-ray emission spectroscopy (XES) has emerged as a power- ful technique for the structural characterization of complex organometallic compounds in realistic environments. Since the spectrum represents electronic transitions from the ligand molecular orbitals to the core holes of the metal centers, the approach is more chemically sensitive to the metal-ligand bonding character compared with con- ventional X-ray absorption techniques. In this paper we study how linear-response time-dependent density functional theory (LR-TDDFT) can be harnessed to simulate K-edge VtC X-ray emission spectra reliably. LR-TDDFT allows one to go beyond the single-particle picture that has been extensively used to simulate VtC-XES. We con- sider seven low- and high-spin model complexes involving chromium, manganese and iron transition metal centers. Our results are in good agreement with experiment.

  7. Controlled variation of the information depth by angle dependent soft X-ray emission spectroscopy: A study on polycrystalline Cu(In,Ga)Se 2

    Science.gov (United States)

    Mönig, H.; Lauermann, I.; Grimm, A.; Camus, C.; Kaufmann, C. A.; Pistor, P.; Jung, Ch.; Kropp, T.; Lux-Steiner, M. C.; Fischer, Ch.-H.

    2008-12-01

    Angle dependent X-ray emission spectroscopy (AXES) is introduced as a tool for depth dependent composition analysis. A controlled variation of the information depth is demonstrated by changing the geometry from grazing exit to grazing incidence geometry. First results are presented from Cu(In,Ga)Se 2 (CIGSe)-based polycrystalline thin film solar cell bi-layer components. A mathematical model explains changes in relative intensity due to the absorption and emission behavior of thin CdS and Zn(S,O) cover layers. The fact that the presented data can be modelled by ideal bi-layer structures, provides both, proof of concept in general and the proof of applicability to the relatively rough layered structures based on CIGSe. In bare CIGSe a homogeneous distribution of Cu and Ga is found in a depth range between 22 and 470 nm.

  8. Determination of nitrous acid emission factors from a gasoline vehicle using a chassis dynamometer combined with incoherent broadband cavity-enhanced absorption spectroscopy.

    Science.gov (United States)

    Nakashima, Yoshihiro; Kajii, Yoshizumi

    2017-01-01

    Nitrous acid (HONO) is a well-known source of hydroxyl radicals in the troposphere. Vehicle exhaust is considered to be one of the primary emission sources of HONO. In this study, measurements of HONO in gasoline vehicle exhaust were carried out using a chassis dynamometer combined with incoherent broadband cavity-enhanced absorption spectroscopy. When catalysts were warm, concentrations of HONO were higher than those prior to catalysts warming. Other species, such as CO, and total hydrocarbons (THCs), showed the opposite pattern. There were no correlations evident between HONO and other trace species concentrations immediately after emission. The HONO/NOx ratio, a good proxy for the formation of HONO in atmosphere, ranged from 1.1 to 6.8×10(-3), which was consistent with previous studies. HONO emission factors (EFs) were calculated to be 0.01-3.6mgkg(-1) fuel, which was different from the vehicle's specifications and those reported under different driving cycles. Annual HONO emissions in Japan were estimated using the calculated EFs and other statistical data. Copyright © 2016 Elsevier B.V. All rights reserved.

  9. The Number Density Evolution of Extreme Emission Line Galaxies in 3D-HST: Results from a Novel Automated Line Search Technique for Slitless Spectroscopy

    CERN Document Server

    Maseda, Michael V; Rix, Hans-Walter; Momcheva, Ivelina; Brammer, Gabriel B; Franx, Marijn; Lundgren, Britt F; Skelton, Rosalind E; Whitaker, Katherine E

    2016-01-01

    The multiplexing capability of slitless spectroscopy is a powerful asset in creating large spectroscopic datasets, but issues such as spectral confusion make the interpretation of the data challenging. Here we present a new method to search for emission lines in the slitless spectroscopic data from the 3D-HST survey utilizing the Wide-Field Camera 3 on board the Hubble Space Telescope. Using a novel statistical technique, we can detect compact (extended) emission lines at 90% completeness down to fluxes of 1.5 (3.0) times 10^{-17} erg/s/cm^2, close to the noise level of the grism exposures, for objects detected in the deep ancillary photometric data. Unlike previous methods, the Bayesian nature allows for probabilistic line identifications, namely redshift estimates, based on secondary emission line detections and/or photometric redshift priors. As a first application, we measure the comoving number density of Extreme Emission Line Galaxies (restframe [O III] 5007 equivalent widths in excess of 500 Angstroms)...

  10. Remote sensing of temperature and concentration profiles of a gas jet by coupling infrared emission spectroscopy and LIDAR for characterization of aircraft engine exhaust

    Science.gov (United States)

    Offret, J.-P.; Lebedinsky, J.; Navello, L.; Pina, V.; Serio, B.; Bailly, Y.; Hervé, P.

    2015-05-01

    Temperature data play an important role in the combustion chamber since it determines both the efficiency and the rate of pollutants emission of engines. Air pollution problem concerns the emissions of gases such as CO, CO2, NO, NO2, SO2 and also aerosols, soot and volatile organic compounds. Flame combustion occurs in hostile environments where temperature and concentration profiles are often not easy to measure. In this study, a temperature and CO2 concentration profiles optical measurement method, suitable for combustion analysis, is discussed and presented. The proposed optical metrology method presents numerous advantages when compared to intrusive methods. The experimental setup comprises a passive radiative emission measurement method combined with an active laser-measurement method. The passive method is based on the use of gas emission spectroscopy. The experimental spectrometer device is coupled with an active method. The active method is used to investigate and correct complex flame profiles. This method similar to a LIDAR (Light Detection And Ranging) device is based on the measurement of Rayleigh scattering of a short laser pulse recorded using a high-speed streak camera. The whole experimental system of this new method is presented. Results obtained on a small-scale turbojet are shown and discussed in order to illustrate the potentials deliver by the sophisticated method. Both temperature and concentration profiles of the gas jet are presented and discussed.

  11. AKARI near-infrared spectroscopy of the extended green object G318.05+0.09: Detection of CO fundamental ro-vibrational emission

    CERN Document Server

    Onaka, Takashi; Sakon, Itsuki; Ardaseva, Aleksandra

    2016-01-01

    We present the results of near-infrared (2.5--5.4um) long-slit spectroscopy of the extended green object (EGO) G318.05+0.09 with AKARI. Two distinct sources are found in the slit. The brighter source has strong red continuum emission with H2O ice, CO2 ice, and CO gas and ice absorption features at 3.0, 4.25um, 4.67um, respectively, while the other greenish object shows peculiar emission that has double peaks at around 4.5 and 4.7um. The former source is located close to the ultra compact HII region IRAS 14498-5856 and is identified as an embedded massive young stellar object. The spectrum of the latter source can be interpreted by blue-shifted (-3000 ~ -6000km/s) optically-thin emission of the fundamental ro-vibrational transitions (v=1-0) of CO molecules with temperatures of 12000--3700K without noticeable H2 and HI emission. We discuss the nature of this source in terms of outflow associated with the young stellar object and supernova ejecta associated with a supernova remnant.

  12. Quantification of fluorine traces in solid samples using CaF molecular emission bands in atmospheric air Laser-Induced Breakdown Spectroscopy

    Science.gov (United States)

    Alvarez-Llamas, C.; Pisonero, J.; Bordel, N.

    2016-09-01

    Direct solid determination of trace amounts of fluorine using Laser-Induced Breakdown Spectroscopy (LIBS) is a challenging task due to the low excitation efficiency of this element. Several strategies have been developed to improve the detection capabilities, including the use of LIBS in a He atmosphere to enhance the signal to background ratios of F atomic emission lines. An alternative method is based on the detection of the molecular compounds that are formed with fluorine in the LIBS plasma. In this work, the detection of CaF molecular emission bands is investigated to improve the analytical capabilities of atmospheric air LIBS for the determination of fluorine traces in solid samples. In particular, Cu matrix samples containing different fluorine concentration (between 50 and 600 μg/g), and variable amounts of Ca, are used to demonstrate the linear relationships between CaF emission signal and F concentration. Limits of detection for fluorine are improved by more than 1 order of magnitude using CaF emission bands versus F atomic lines, in atmospheric-air LIBS. Furthermore, a toothpaste powder sample is used to validate this analytical method. Good agreement is observed between the nominal and the predicted fluorine mass-content.

  13. Heterogeneity in optical properties of near white-light emissive europium complex species revealed by spectroscopy of single nanoaggregates

    Science.gov (United States)

    Irfanullah, Mir; Sharma, Dharmendar Kumar; Chulliyil, Ramya; Layek, Arunasish; De, Suman; Chowdhury, Arindam

    2017-01-01

    Photoluminescence microscopy has been used to interrogate individual nanoaggregates (NAs) of visible light excitable Eu(III)-complex species with 9-hydroxyphenalenone which we found to emit near-white light in methanol. In the solid state however, NAs display diverse emission spectra due to varied sensitization efficiencies, and thereby exhibit a wide range of emission colours. Heterogeneity in sensitization efficiency and asymmetry ratios for Eu-emission is intriguing because all measurable photoluminescence parameters are expected to average out over large number of Eu-complex species which constitute NAs, and suggests the existence of relatively few yet efficient Eu3+ radiative trap centres of varied asymmetry within NAs.

  14. Study on Emission Spectral Lines of Iron, Fe in Laser-Induced Breakdown Spectroscopy (LIBS) on Soil Samples

    Science.gov (United States)

    Idris, Nasrullah; Lahna, Kurnia; Fadhli; Ramli, Muliadi

    2017-05-01

    In this work, LIBS technique has been used for detection of heavy metal especially iron, Fe in soil sample. As there are a large number of emission spectral lines due to Fe and other constituents in soil, this study is intended to identify emission spectral lines of Fe and finally to find best fit emission spectral lines for carrying out a qualitative and quantitative analysis. LIBS apparatus used in this work consists of a laser system (Neodymium Yttrium Aluminum Garnet, Nd-YAG: Quanta Ray; LAB SERIES; 1,064 nm; 500 mJ; 8 ns) and an optical multichannel analyzer (OMA) system consisting of a spectrograph (McPherson model 2061; 1,000 mm focal length; f/8.6 Czerny- Turner) and an intensified charge coupled device (ICCD) 1024x256 pixels (Andor I*Star). The soil sample was collected from Banda Aceh city, Aceh, Indonesia. For spectral data acquisition, the soil sample has been prepared by a pressing machine in the form of pellet. The laser beam was focused using a high density lens (f=+150 mm) and irradiated on the surface of the pellet for generating luminous plasma under 1 atmosphere of air surrounding. The plasma emission was collected by an optical fiber and then sent to the optical multichannel analyzer (OMA) system for acquisition of the emission spectra. It was found that there are many Fe emission lines both atomic lines (Fe I) and ionic lines (Fe II) appeared in all detection windows in the wavelength regions, ranging from 200 nm to 1000 nm. The emission lines of Fe with strong intensities occurs together with emission lines due to other atoms such as Mg, Ca, and Si. Thus, the identification of emission lines from Fe is complicated by presence of many other lines due to other major and minor elements in soil. Considering the features of the detected emission lines, several emission spectral lines of Fe I (atomic emission line), especially Fe I 404.58 nm occurring at visible range are potential to be good candidate of analytical lines in relation to detection

  15. Evaluation of Optical Depths and Self-Absorption of Strontium and Aluminum Emission Lines in Laser-Induced Breakdown Spectroscopy (LIBS).

    Science.gov (United States)

    Alfarraj, Bader A; Bhatt, Chet R; Yueh, Fang Yu; Singh, Jagdish P

    2017-04-01

    Laser-induced breakdown spectroscopy (LIBS) is a widely used laser spectroscopic technique in various fields, such as material science, forensic science, biological science, and the chemical and pharmaceutical industries. In most LIBS work, the analysis is performed using radiative transitions from atomic emissions. In this study, the plasma temperature and the product [Formula: see text] (the number density N and the absorption path length [Formula: see text]) were determined to evaluate the optical depths and the self-absorption of Sr and Al lines. A binary mixture of strontium nitrate and aluminum oxide was used as a sample, consisting of variety of different concentrations in powder form. Laser-induced breakdown spectroscopy spectra were collected by varying various parameters, such as laser energy, gate delay time, and gate width time to optimize the LIBS signals. Atomic emission from Sr and Al lines, as observed in the LIBS spectra of different sample compositions, was used to characterize the laser induced plasma and evaluate the optical depths and self-absorption of LIBS.

  16. Measurements of plasma temperature and electron density in laser-induced copper plasma by time-resolved spectroscopy of neutral atom and ion emissions

    Indian Academy of Sciences (India)

    V K Unnikrishnan; Kamlesh Alti; V B Kartha; C Santhosh; G P Gupta; B M Suri

    2010-06-01

    Plasma produced by a 355 nm pulsed Nd:YAG laser with a pulse duration of 6 ns focussed onto a copper solid sample in air at atmospheric pressure is studied spectroscopically. The temperature and electron density characterizing the plasma are measured by time-resolved spectroscopy of neutral atom and ion line emissions in the time window of 300–2000 ns. An echelle spectrograph coupled with a gated intensified charge coupled detector is used to record the plasma emissions. The temperature is obtained using the Boltzmann plot method and the electron density is determined using the Saha– Boltzmann equation method. Both parameters are studied as a function of delay time with respect to the onset of the laser pulse. The results are discussed. The time window where the plasma is optically thin and is also in local thermodynamic equilibrium (LTE), necessary for the laser-induced breakdown spectroscopy (LIBS) analysis of samples, is deduced from the temporal evolution of the intensity ratio of two Cu I lines. It is found to be 700–1000 ns.

  17. GRB hosts through cosmic time - VLT/X-shooter emission-line spectroscopy of 96 GRB-selected galaxies at 0.1 < z < 3.6

    CERN Document Server

    Krühler, T; Fynbo, J P U; Hartoog, O E; Hjorth, J; Jakobsson, P; Perley, D A; Rossi, A; Schady, P; Schulze, S; Tanvir, N R; Vergani, S D; Wiersema, K; Afonso, P M J; Bolmer, J; Cano, Z; Covino, S; D'Elia, V; Postigo, A de Ugarte; Filgas, R; Friis, M; Graham, J F; Greiner, J; Goldoni, P; Gomboc, A; Hammer, F; Japelj, J; Kann, D A; Kaper, L; Klose, S; Levan, A J; Leloudas, G; Milvang-Jensen, B; Guelbenzu, A Nicuesa; Palazzi, E; Pian, E; Piranomonte, S; Sanchez-Ramirez, R; Savaglio, S; Selsing, J; Tagliaferri, G; Vreeswijk, P M; Watson, D J; Xu, D

    2015-01-01

    We present data and initial results from VLT/X-shooter emission-line spectroscopy of 96 GRB-selected galaxies at 0.1spectroscopy available to date. The majority of our GRBs was detected by Swift and 76% are at 0.5emission-line widths (sigma). We find a strong change of the typical physical properties of GRB hosts with redshift. The median SFR, for example, increases from ~0.6 M_sun/yr at z~0.6 up to ~15 M_sun/yr at z~2. A higher ratio of [OIII]/[OII] at higher redshifts leads to an increasing distance of GRB-selected galaxies to the locus of local galaxies in the BPT diagram. Oxygen abundances of the galaxies are distributed between 12+log(O/H)=7.9 and 12+log(O/H)=9.0 with a median of 12+log(O/H)~8.5. The fraction of GRB-selected galaxies with super-solar metallic...

  18. Optical emission spectroscopy study of the expansion dynamics of a laser generated plasma during the deposition of thin films by laser ablation

    Directory of Open Access Journals (Sweden)

    Fazio, Enza

    2007-09-01

    Full Text Available The dynamics of the expanding plasma produced by excimer laser ablation of different materials such as silicon, silicon carbide, graphite and tin powder were studied by means of time integrated, spatially resolved emission spectroscopy and fast photography imaging of the expanding plasma. Experiments were performed both in vacuum and in different pure background atmosphere (i.e. oxygen or nitrogen and, finally, in gaseous mixtures (i.e. in O2/Ar and N2/Ar mixtures. These investigations were performed to gather information on the nature of the chemical species present in the plasma and on the occurrence of chemical reactions during the interaction between the plasma and the background gas. Then, we tried to correlate the plasma expansion dynamics to the structural and physical properties of the deposited materials. Experimental results clearly indicate that there is a strong correlation between the plasma expansion dynamics and the structural properties of the deposited thin films. In this respect, the investigations performed by means of fast photography and of optical emission spectroscopy revealed themselves as powerful tools for an efficient control of the deposition process itself.

  19. Potential radionuclide emissions from stacks on the Hanford site, Part 2: Dose assessment methodology using portable low-resolution gamma spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Barnett, J.M. [Westinghouse Hanford Company, Richland, WA (United States)

    1995-02-01

    In September 1992, the Westinghouse Hanford Company began developing an in situ measurement method to assess gamma radiation emanating from high-efficiency particulate air filters using portable low-resolution gamma spectroscopy. The purpose of the new method was to assess radioactive exhaust stack air emissions from empirical data rather than from theoretical models and to determine the potential unabated dose to an offsite theoretical maximally exposed individual. In accordance with Title 40, Code of Federal Regulations, Part 61, Subpart H, {open_quotes}National Emission Standards for Hazardous Air Pollutants{close_quotes}, stacks that have the potential to emit {ge} 1 {mu}Sv y{sup {minus}1} (0.1 mrem y{sup {minus}1}) to the maximally exposed individual are considered {open_quotes}major{close_quotes} and must meet the continuous monitoring requirements. After the method was tested and verified, the U.S. Environmental Protection Agency, Region 10, approved its use in June 1993. Of the 125 stacks operated by the Westinghouse Hanford Company, 22 were targeted for evaluation by this method, and 15 were assessed. (The method could not be applied at seven stacks because of excessive background radiation or because no gamma emitting particles appear in the emission stream.) The most significant result from this study was the redesignation of the T Plant main stack. The stack was assessed as being {open_quotes}minor{close_quotes}, and it now only requires periodic confirmatory measurements and meets federally imposed sampling requirements.

  20. Exploration of CdTe quantum dots as mesoscale pressure sensors via time-resolved shock-compression photoluminescent emission spectroscopy

    Science.gov (United States)

    Kang, Zhitao; Banishev, Alexandr A.; Lee, Gyuhyon; Scripka, David A.; Breidenich, Jennifer; Xiao, Pan; Christensen, James; Zhou, Min; Summers, Christopher J.; Dlott, Dana D.; Thadhani, Naresh N.

    2016-07-01

    The nanometer size of CdTe quantum dots (QDs) and their unique optical properties, including size-tunable narrow photoluminescent emission, broad absorption, fast photoluminescence decay, and negligible light scattering, are ideal features for spectrally tagging the shock response of localized regions in highly heterogeneous materials such as particulate media. In this work, the time-resolved laser-excited photoluminescence response of QDs to shock-compression was investigated to explore their utilization as mesoscale sensors for pressure measurements and in situ diagnostics during shock loading experiments. Laser-driven shock-compression experiments with steady-state shock pressures ranging from 2.0 to 13 GPa were performed on nanocomposite films of CdTe QDs dispersed in a soft polyvinyl alcohol polymer matrix and in a hard inorganic sodium silicate glass matrix. Time-resolved photoluminescent emission spectroscopy was used to correlate photoluminescence changes with the history of shock pressure and the dynamics of the matrix material surrounding the QDs. The results revealed pressure-induced blueshifts in emitted wavelength, decreases in photoluminescent emission intensity, reductions in peak width, and matrix-dependent response times. Data obtained for these QD response characteristics serve as indicators for their use as possible time-resolved diagnostics of the dynamic shock-compression response of matrix materials in which such QDs are embedded as in situ sensors.

  1. Spatio-spectral characteristics of ultra-broadband THz emission from two-colour photoexcited gas plasmas and their impact for nonlinear spectroscopy

    Science.gov (United States)

    Blank, V.; Thomson, M. D.; Roskos, H. G.

    2013-07-01

    We present a characterization of the combined spatial and spectral properties of the terahertz (THz) and mid-infrared emission from gas plasmas generated and driven by two-colour femtosecond optical pulses. For its use in nonlinear spectroscopy, the impact of the relatively complex spatial profile for both broadband (∼ 10 THz) and ultra-broadband (> 100 THz) emission needs to be considered, in particular for experiments based on z-scan techniques. Here we apply spatially resolved measurements based on both field autocorrelation and sum-frequency (up-conversion) detection. Based on these results, we present simulations of the ultra-broadband profile during its passage through a focal region. In addition to the inherent features of the emission profile due to the generation mechanism in the plasma filament, we also analyse the role of the semconductor (silicon) wafer typically placed after the plasma to discard the optical pump beams, whose photoexcitation also can play a role in the resultant THz profile.

  2. In situ diagnosis of pulsed UV laser surface ablation of tungsten carbide hardmetal by using laser-induced optical emission spectroscopy

    Science.gov (United States)

    Li, Tiejun; Lou, Qihong; Wei, Yunrong; Huang, Feng; Dong, Jingxing; Liu, Jingru

    2001-12-01

    Surface ablation of cobalt cemented tungsten carbide hardmetal with pulsed UV laser has been in situ diagnosed by using the technique of laser-induced optical emission spectroscopy. The dependence of emission intensity of cobalt lines on number of laser shots was investigated at laser fluence of 2.5 J/cm 2. As a comparison, the reliance of emission intensity of cobalt lines as a function of laser pulse number by using pure cobalt as ablation sample was also studied at the same laser condition. It was found that for surface ablation of tungsten carbide hardmetal at laser fluence of 2.5 J/cm 2, the intensities of cobalt lines fell off dramatically in the first 300 consecutive laser shots and then slowed down to a low stable level with even more shots. For surface ablation of pure cobalt at the same laser condition, the intensities of cobalt lines remained constant more or less even after 500 laser shots and then reduced very slowly with even more shots. It was concluded that selective evaporation of cobalt at this laser fluence should be responsible for the dramatic fall-off of cobalt lines with laser shots accumulation for surface ablation of tungsten carbide hardmetal. In contrast, for surface ablation of pure cobalt, the slow reduction of cobalt lines with pulse number accumulation should be due to the formation of laser-induced crater effect.

  3. Photolysis of n-butyl nitrite and isoamyl nitrite at 355 nm: A time-resolved Fourier transform infrared emission spectroscopy and ab initio study

    CERN Document Server

    Ji, Min; Zhang, Qun; Chen, Yang

    2009-01-01

    We report on the photodissociation dynamics study of n-butyl nitrite (n-C_4H_9ONO) and isoamyl nitrite ((CH_3)_2C_3H_5ONO) by means of time-resolved Fourier transform infrared (TR-FTIR) emission spectroscopy. The obtained TR-FTIR emission spectra of the nascent NO fragments produced in the 355-nm laser photolysis of the two alkyl nitrite species showed an almost identical rotational temperature and vibrational distributions of NO. In addition, a close resemblance between the two species was also found in the measured temporal profiles of the IR emission of NO and the recorded UV absorption spectra. The experimental results are consistent with our ab initio calculations using the time-dependent density functional theory at the B3LYP/6-311G(d,p) level, which indicate that the substitution of one of the two {gamma}-H atoms in n-C_4H_9ONO with a methyl group to form (CH_3)_2C_3H_5ONO has only a minor effect on the photodissociation dynamics of the two molecules.

  4. Interactions of protons with furan molecules studied by collision-induced emission spectroscopy at the incident energy range of 50-1000 eV

    Science.gov (United States)

    Wasowicz, Tomasz J.; Pranszke, Boguslaw

    2016-08-01

    Investigations of the ion-molecule reactions provide insight into many fields ranging from the stellar wind interaction with interstellar media, up to medicine and industrial applications. Besides the applications, the understanding of these processes is itself a problem of fundamental importance. Thus, interactions of protons with the gas-phase furan molecules have been investigated for the first time in the energy range of 50-1000 eV exploiting collision-induced emission spectroscopy. Recorded spectra reveal emission of the atomic H β to H θ lines of the hydrogen Balmer series and the molecular bands of vibrationally and rotationally excited diatomic CH fragments created in the A2 Δ and B2Σ- electronic states. The measurements of the emission yields of the excited fragments by recording their intensities at different projectile energies have been performed. The highest yields have been observed for production of hydrogen atoms which intensities rapidly decreased with increasing principal quantum number n . From the H ( n = 4-7) intensity ratios depopulation factors of hydrogen excited states have been determined at each impact energy and possible collisional mechanisms leading to enhanced production of the hydrogen atoms have been suggested. We compare and discuss our results with improved data set of proton collisions with tetrahydrofuran (THF) molecules, the hydrogenated derivatives of furan.

  5. Time-resolved measurement of atomic emission enhancement by fs-ns dual-pulsed laser-induced breakdown spectroscopy

    Institute of Scientific and Technical Information of China (English)

    Yan Li-Xin; Zhang Yong-Sheng; Zheng Guo-Xin; Liu Jing-Ru; Cheng Jian-Ping; Lü Min

    2006-01-01

    Time-resolved measurement of atomic emission enhancement is performed by using a 500-fs KrF laser pulse incident upon a high density supersonic O2 gas jet, synchronized with an orthogonal ns frequency-doubled Nd:YAG laser pulse. The ultra-short pulse serves as an igniter of the gas jet, and the subsequent ns-laser pulse significantly enhances the atomic emission. Analysis shows that the contributions to the enhancement effect are made mainly by the bremsstrahlung radiation and cascade ionization.

  6. Standard test method for determination of impurities in plutonium: acid dissolution, ion exchange matrix separation, and inductively coupled plasma-atomic emission spectroscopic (ICP/AES) analysis

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2003-01-01

    1.1 This specification covers blended uranium trioxide (UO3), U3O8, or mixtures of the two, powders that are intended for conversion into a sinterable uranium dioxide (UO2) powder by means of a direct reduction process. The UO2 powder product of the reduction process must meet the requirements of Specification C 753 and be suitable for subsequent UO2 pellet fabrication by pressing and sintering methods. This specification applies to uranium oxides with a 235U enrichment less than 5 %. 1.2 This specification includes chemical, physical, and test method requirements for uranium oxide powders as they relate to the suitability of the powder for storage, transportation, and direct reduction to UO2 powder. This specification is applicable to uranium oxide powders for such use from any source. 1.3 The scope of this specification does not comprehensively cover all provisions for preventing criticality accidents, for health and safety, or for shipping. Observance of this specification does not relieve the user of th...

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

    Science.gov (United States)

    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.

  8. Effect of HF addition on the microwave-assisted acid-digestion for the determination of metals in coal by inductively coupled plasma-atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Yan-Hua [Department of Environmental Science and Engineering, College of Urban Construction and Safety and Environmental Engineering, Nanjing University of Technology, No. 200 Zhongshan Beilu, Nanjing 210009, Jiangsu (China); Iwashita, A.; Nakajima, T.; Yamashita, H.; Takanashi, H.; Ohki, A. [Department of Bioengineering, Faculty of Engineering, Kagoshima University, 1-21-40, Korimoto, Kagoshima 890-0065 (Japan)

    2005-03-31

    The microwave-assisted acid-digestion for the determination of metals in coal by ICP-AES was investigated, especially focusing on the necessity of adding HF. By testing five certified reference materials, BCR-180, BCR-040, NIST-1632b, NIST-1632c, and SARM-20, it was found that the two-stage digestion without HF (HNO{sub 3}+H{sub 2}O{sub 2} was used) was very effective for the pretreatment of ICP-AES measurement. Both major metals (Al, Ca, Fe, and Mg) and minor or trace metals (Co, Cr, Cu, Mn, Ni, Pb, and Zn) in coal gave good recoveries for their certified or reference values. The possibility of 'HF-memory effect' was cancelled by the use of a set of vessels which had been never contacted with HF. Twenty-four Japanese standard coals (SS coals) were analyzed by the present method, and the concentrations of major metals measured by the present method provided very high accordance with those from the authentic JIS (Japanese Industrial Standard) method.

  9. Effect of HF addition on the microwave-assisted acid-digestion for the determination of metals in coal by inductively coupled plasma-atomic emission spectrometry.

    Science.gov (United States)

    Xu, Yan-Hua; Iwashita, Akira; Nakajima, Tsunenori; Yamashita, Hiroyuki; Takanashi, Hirokazu; Ohki, Akira

    2005-03-31

    The microwave-assisted acid-digestion for the determination of metals in coal by ICP-AES was investigated, especially focusing on the necessity of adding HF. By testing five certified reference materials, BCR-180, BCR-040, NIST-1632b, NIST-1632c, and SARM-20, it was found that the two-stage digestion without HF (HNO(3)+H(2)O(2) was used) was very effective for the pretreatment of ICP-AES measurement. Both major metals (Al, Ca, Fe, and Mg) and minor or trace metals (Co, Cr, Cu, Mn, Ni, Pb, and Zn) in coal gave good recoveries for their certified or reference values. The possibility of 'HF-memory effect' was cancelled by the use of a set of vessels which had been never contacted with HF. Twenty-four Japanese standard coals (SS coals) were analyzed by the present method, and the concentrations of major metals measured by the present method provided very high accordance with those from the authentic JIS (Japanese Industrial Standard) method.

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

    Science.gov (United States)

    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.

  11. Simultaneous preconcentration of copper and mercury in water samples by cloud point extraction and their determination by inductively coupled plasma atomic emission spectrometry

    Science.gov (United States)

    Shoaee, Hamta; Roshdi, Mina; Khanlarzadeh, Nasibeh; Beiraghi, Asadollah

    2012-12-01

    A cloud-point extraction process coupled to ICP-OES by using 3-nitro benzaldehyde thiosemicarbazone (3-NBT) as complexing agent was developed for the simultaneous preconcentration and determination of copper and mercury in water samples. The variables affecting the complexation and extraction steps were optimized. Under the optimum conditions (i.e. 1.5 × 10-5 mol L-1 ligand, 0.3% (v/v) Triton X-114, 55 °C equilibrium temperature, incubation time of 30 min) the calibration graphs were linear in the range of 5-120 and 10-100 ng mL-1 with enhancement factor of 82.7 and 51.3 for Cu2+ and Hg2+, respectively. The preconcentration factors were 28.6 in both cases and detection limits were obtained 0.48 for Cu and 1.1 ng mL-1 for Hg. The precisions (R.S.D.%) for five replicate determinations at 50 ng mL-1 of copper and mercury were better than 1.8% and 3.2%, respectively. The accuracy of the proposed method is validated by analyzing a certified reference material of water (RTC-QCI-049) with satisfactory results. Finally, the proposed method was utilized successfully for the determination of copper and mercury in surface water (river), tap water and bottled mineral water samples.

  12. Purge-and-trap isothermal multicapillary gas chromatographic sample introduction accessory for speciation of mercury by microwave-induced plasma atomic emission spectrometry.

    Science.gov (United States)

    Rodriguez Pereiro, I; Wasik, A; Lobiński, R

    1998-10-01

    A compact device based on purge-and-trap multicapillary gas chromatography was developed for sensitive species-selective analysis of methylmercury and Hg2+ by atomic spectrometry. The operating mode includes in situ conversion of the analyte species to MeEtHg and HgEt2 and cryotrapping of the derivatives formed in a 0.53-mm-i.d. capillary, followed by their flash ( 60 mL min-1) compatible with an MIP AES detector (no dilution with a makeup gas is required). Developments regarding each of the steps of the analytical procedure and effects of operational variables (sample volume, purge flow, trap temperature, separation conditions) are discussed. The device allows speciation of MeHg+ and Hg2+ down to 5 pg g-1 in urine and, after a rapid microwave-assisted hydrolysis, down to 0.1 ng g-1 in solid biological samples with a throughput of 6 samples/h. The analytical protocols developed were validated by the analysis of DORM-1 (dogfish muscle), TORT-1 (lobster hepatopancreas), and Seronorm urine certified reference materials.

  13. Preconcentration of Rare Earth Elements with 8-Hydroxyquinoline-5-sulfonic Acid Chelated Cellulose Filter Prior to Determination by Inductively Coupled Plasma Atomic Emission Spectrometry

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    8-Hydroxyquinoline-5-sulfonic acid,covalently bound to filter cellulose,was used for preconcentrating trace rare earth element(REE) ions from complex matrices and matrix separation,respectively.Multi-REE ions were preconcentrated on the column filled with 8-hydroxyquinoline-5-sulfonic acid cellulose filter and analysed by ICP-AES after being eluted with dilute HNO3.In the given pH range,alkali and alkaline earth metal ions can be separated as matrix elements;a high concentration factor is obtained and the eluates can be measured without interference.The usefulness of the method is shown by the control analyses of standard reference materials.

  14. Simultaneous preconcentration of copper and mercury in water samples by cloud point extraction and their determination by inductively coupled plasma atomic emission spectrometry.

    Science.gov (United States)

    Shoaee, Hamta; Roshdi, Mina; Khanlarzadeh, Nasibeh; Beiraghi, Asadollah

    2012-12-01

    A cloud-point extraction process coupled to ICP-OES by using 3-nitro benzaldehyde thiosemicarbazone (3-NBT) as complexing agent was developed for the simultaneous preconcentration and determination of copper and mercury in water samples. The variables affecting the complexation and extraction steps were optimized. Under the optimum conditions (i.e. 1.5×10(-5) mol L(-1) ligand, 0.3% (v/v) Triton X-114, 55 °C equilibrium temperature, incubation time of 30 min) the calibration graphs were linear in the range of 5-120 and 10-100 ng mL(-1) with enhancement factor of 82.7 and 51.3 for Cu(2+) and Hg(2+), respectively. The preconcentration factors were 28.6 in both cases and detection limits were obtained 0.48 for Cu and 1.1 ng mL(-1) for Hg. The precisions (R.S.D.%) for five replicate determinations at 50 ng mL(-1) of copper and mercury were better than 1.8% and 3.2%, respectively. The accuracy of the proposed method is validated by analyzing a certified reference material of water (RTC-QCI-049) with satisfactory results. Finally, the proposed method was utilized successfully for the determination of copper and mercury in surface water (river), tap water and bottled mineral water samples.

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

    NARCIS (Netherlands)

    Derksen-van Gastelen, Sanne; Dijkstra, Jan

    2016-01-01

    Enteric methane (CH4) production is among the main targets of greenhouse gas mitigation practices for the dairy industry. A simple, robust and inexpensive measurement technique applicable on a large scale to estimate CH4 emission from dairy cattle would therefore be valuable

  16. Near-Infrared Spectroscopy of Faint Discrete X-ray Point Sources Constituting the Galactic Ridge X-ray Emission

    CERN Document Server

    Morihana, Kumiko; Dubath, Pierre; Yoshida, Tessei; Suzuki, Kensuke; Ebisawa, Ken

    2016-01-01

    The Galactic Ridge X-ray Emission (GRXE) is apparently extended X-ray emission along the Galactic Plane. The X-ray spectrum is characterized by hard continuum with a strong Fe K emission feature in the 6-7 keV band. A substantial fraction (~80%) of the GRXE in the Fe band was resolved into point sources by deep Chandra imaging observations, thus GRXE is mostly composed of dim Galactic X-ray point sources at least in this energy band. To investigate the populations of these dim X-ray point sources, we carried out Near-Infrared (NIR) follow-up spectroscopic observations in two deep Chandra fields located in the Galactic plane at (l,b)=(0.1{\\arcdeg}, -1.4{\\arcdeg}) and (28.5{\\arcdeg}, 0.0{\\arcdeg}) using NTT/SofI and Subaru/MOIRCS. We obtained well-exposed NIR spectra from 65 objects and found that there are three main classes of Galactic sources based on the X-ray color and NIR spectral features: those having (A) hard X-ray spectra and NIR emission features such as HI(Br{\\gamma}), HeI, and HeII (2 objects), (B)...

  17. Predicting methane emissions of lactating Danish Holstein cows using Fourier transform mid-infrared spectroscopy of milk

    NARCIS (Netherlands)

    Shetty, N.P.; Difford, G.; Lassen, J.; Løvendahl, P.; Buitenhuis, A.J.

    2017-01-01

    Enteric methane (CH4), a potent greenhouse gas, is among the main targets of mitigation practices for the dairy industry. A measurement technique that is rapid, inexpensive, easy to use, and applicable at the population level is desired to estimate CH4 emission from dairy cows. In the present study,

  18. A comparison of simultaneous plasma, atomic absorption, and iron colorimetric determinations of major and trace constituents in acid mine waters

    Science.gov (United States)

    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. Advanced techniques for actinide spectroscopy (ATAS 2012). Abstract book

    Energy Technology Data Exchange (ETDEWEB)

    Foerstendorf, Harald; Mueller, Katharina; Steudtner, Robin (eds.)

    2012-07-01

    The abstract book of the International workshop on advanced techniques for actinide spectroscopy (ATAS 2012) include contributions concerning the following issues: environmental applications, NMR spectroscopy, vibrational spectroscopy, X-ray spectroscopy and theory, technical application: separation processes, emission spectroscopy.

  20. Observation of Atomic Emission Enhancement by fs-ns Dual-Pulse Laser-Induced Breakdown Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    YAN Li-Xin; ZHANG Yong-Sheng; ZHANG Li-Rong; LIU Jing-Ru; CHENG Jian-Ping; L(U) Min

    2006-01-01

    An experiment of a 500-fs KrF laser pulse incident upon a high density supersonic O2 gas jet synchronously with an ns frequency-doubled Nd:YAG laser pulse is performed in orthogonal configuration.Significant atomic emission enhancement of over forty-fold is observed with an optical multi-channel analyser.The enhancement effect is probably attributed to the different ionization mechanisms between fs and ns laser pulses.

  1. Electron density in amplitude modulated microwave atmospheric plasma jet as determined from microwave interferometry and emission spectroscopy

    Science.gov (United States)

    Faltýnek, J.; Hnilica, J.; Kudrle, V.

    2017-01-01

    Time resolved electron density in an atmospheric pressure amplitude modulated microwave plasma jet is determined using the microwave interferometry method, refined by numerical modelling of the propagation of non-planar electromagnetic waves in the vicinity of a small diameter, dense collisional plasma filament. The results are compared to those from the Stark broadening of the {{\\text{H}}β} emission line. Both techniques show, both qualitatively and quantitatively, a similar temporal evolution of electron density during one modulation period.

  2. Excited State Chemistry in the Free Stream of the NASA IHF Arc Jet Facility Observed by Emission Spectroscopy

    Science.gov (United States)

    Winter, Michael W.; Prabhu, Dinesh K.

    2011-01-01

    Spectroscopic measurements of non-equilibrium emission were made in the free stream of the 60 megawatts Interaction Heating Facility at NASA Ames Research Center. In the visible near infrared wavelength region, the most prominent emission was from molecular N2, and in the ultra violet region, the spectra were dominated by emission from molecular NO. The only atomic lines observed were those of copper (an erosion product of the electrodes). The bands of the 1st Positive system of N2 (if B is true then A is true) differed significantly from spectra computed spectra assuming only thermal excitation, suggesting overpopulation of the high vibrational states of the B state of N2. Populations of these high vibrational levels (peaking at v (sub upper) equals 13) of the N2 B state were determined by scaling simulated spectra; calculations were performed for each upper vibrational state separately. The experimental-theoretical procedure was repeated for several radial positions away from the nozzle axis to obtain spatial distributions of the upper state populations; rotational symmetry of the flow was assumed in simulations. The overpopulation of the high vibrational levels has been interpreted as the effect of inverse pre-dissociation of neutral atoms in the N2 A state, which populates the N2 B state through a level crossing process at v (sub upper) is greater than 10.

  3. Influence of COsub>2sub> pressure on the emission spectra and plasma parameters in underwater laser-induced breakdown spectroscopy.

    Science.gov (United States)

    Goueguel, Christian L; McIntyre, Dustin L; Jain, Jinesh C

    2016-12-01

    Optical emission spectroscopic studies have been carried out to investigate the pressure effect of COsub>2sub> on laser-produced underwater plasma. The plasma was generated by focusing 1064 nm, 6 ns pulses from a Nd:YAG laser in a COsub>2sub>-bearing solution. The temporal evolution of the continuum emission, Sr and Ba lines, and plasma electron density and temperature was characterized under COsub>2sub> pressure ranging from 10 to 300 bars. The electron density measurements were made using the Stark broadening of the 455.40 nm Ba II line, while the temperature measurements have been performed by the Saha-Boltzmann method using the Sr I-II lines at 460.73 and 407.77 nm, respectively. It was found that COsub>2sub> pressure has little effect on the emission line intensity and signal-to-background ratio. The electron density and the temperature are found to be independent of the COsub>2sub> pressure at early times. When time becomes longer, the electron density exhibits an appreciable rise as the COsub>2sub> pressure increases, while the temperature is found to be unchanged.

  4. Observation of Coriolis Coupling between nu(2) + 4nu(4) and 7nu(4) in Acetylene &Xtilde;(1)Sigma(+)(g) by Stimulated Emission Pumping Spectroscopy.

    Science.gov (United States)

    Moss; Duan; Jacobson; O'Brien; Field

    2000-02-01

    Stimulated emission pumping (SEP) spectroscopy has been used to examine a low energy region (E(vib) approximately 4400 cm(-1)) of &Xtilde;(1)Sigma(+)(g) acetylene at higher resolution than was possible in previous dispersed fluorescence studies. The expected bright state, nu(2) + 4nu(4), is observed to be coupled to the nearly degenerate 7nu(4) state by a Coriolis mechanism. A least-squares analysis yields values for zero-order vibrational energies, rotational constants, and a Coriolis-coupling coefficient that are all consistent with expectations. Calculated relative intensities of SEP transitions, accounting for interference due to axis-switching effects, are also consistent with observations. Implications of the observed Coriolis resonance with regard to global acetylene vibrational dynamics are also discussed. Copyright 2000 Academic Press.

  5. Current opportunities and challenges of magnetic resonance spectroscopy, positron emission tomography, and mass spectrometry imaging for mapping cancer metabolism in vivo.

    Science.gov (United States)

    Lin, Gigin; Chung, Yuen-Li

    2014-01-01

    Cancer is known to have unique metabolic features such as Warburg effect. Current cancer therapy has moved forward from cytotoxic treatment to personalized, targeted therapies, with some that could lead to specific metabolic changes, potentially monitored by imaging methods. In this paper we addressed the important aspects to study cancer metabolism by using image techniques, focusing on opportunities and challenges of magnetic resonance spectroscopy (MRS), dynamic nuclear polarization (DNP)-MRS, positron emission tomography (PET), and mass spectrometry imaging (MSI) for mapping cancer metabolism. Finally, we highlighted the future possibilities of an integrated in vivo PET/MR imaging systems, together with an in situ MSI tissue analytical platform, may become the ultimate technologies for unraveling and understanding the molecular complexities in some aspects of cancer metabolism. Such comprehensive imaging investigations might provide information on pharmacometabolomics, biomarker discovery, and disease diagnosis, prognosis, and treatment response monitoring for clinical medicine.

  6. Analysis of the absorption spectra of gas emission of patients with lung cancer and chronic obstructive pulmonary disease by laser optoacoustic spectroscopy

    Science.gov (United States)

    Bukreeva, Ekaterina B.; Bulanova, Anna A.; Kistenev, Yurii V.; Kuzmin, Dmitry A.; Tuzikov, Sergei A.; Yumov, Evgenii L.

    2013-02-01

    It is important to identify patients with chronic obstructive pulmonary disease (COPD) and lung cancer in the early stages of the disease. The method of laser opto-acoustic gas analysis, in this case, can act as a promising tool for diagnostics. The material for this study were the gas emission samples collected from patients and healthy volunteers - samples of exhaled air, swabs from teeth and cheeks. A set of material was formed three groups: healthy volunteers, patients with COPD, lung cancer patients. The resulting samples were analyzed by means of laser opto-acoustic gas analyzers: with intracavity location detector (ILPA-1), with extracavity location detector (LGA-2). Presentation of the results in an easy to visual form was performed using the method of elastic maps, based on the principal component analysis. The results of analysis show potentialities of usage of laser optoacoustic spectroscopy application to assess the status of patients with chronic obstructive pulmonary disease and lung cancer.

  7. Delocalization and occupancy effects of 5f orbitals in plutonium intermetallics using L3-edge resonant X-ray emission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Booth, C. H.; Medling, S. A.; Jiang, Yu; Bauer, E. D.; Tobash, P. H.; Mitchell, J. N.; Veirs, D. K.; Wall, M. A.; Allen, P. G.; Kas, J. J.; Sokaras, D.; Nordlund, D.; Weng, T. -C.

    2014-06-24

    Although actinide (An) L3 -edge X-ray absorption near-edge structure (XANES) spectroscopy has been very effective in determining An oxidation states in insulating, ionically bonded materials, such as in certain coordination compounds and mineral systems, the technique fails in systems featuring more delocalized 5f orbitals, especially in metals. Recently, actinide L3-edge resonant X-ray emission spec- troscopy (RXES) has been shown to be an effective alternative. This technique is further demonstrated here using a parameterized partial unoccupied density of states method to quantify both occupancy and delocalization of the 5f orbital in ?-Pu, ?-Pu, PuCoGa5 , PuCoIn5 , and PuSb2. These new results, supported by FEFF calculations, highlight the effects of strong correlations on RXES spectra and the technique?s ability to differentiate between f-orbital occupation and delocalization.

  8. Energy-dispersive x-ray fluorescence spectroscopy and inductively coupled plasma emission spectrometry evaluated for multielement analysis in complex biological matrices.

    Science.gov (United States)

    Irons, R D; Schenk, E A; Giauque, R D

    1976-12-01

    Energy-dispersive x-ray spectroscopy and inductively coupled plasma emission spectrometry were evaluated as methods for routine multielement analysis of biological material. Standard samples included Standard Reference Materials (National Bureau of Standards), compounded mixtures, and supplements that provided a wide range of elemental concentrations for analysis. Elements included in this study were Zn, Pb, Ni, Mn, Fe, Mg, Cu, Ca, As, Se, Br, Rb, and Sr. Standards were analyzed as unknowns by participating laboratories. The two methods were evaluated for sensitivity, precision, and accuracy, and the results compared to those obtained for atomic absorption spectrometric analysis of identical standard unknowns. Both methods compared favorably and both were determined to be highly reliable for such an application. Advantages and disadvantages of each method are compared and discussed.

  9. Study of effect of H2 addition on the production of fluorocarbon radicals in H2/C4F8 inductively coupled plasma via optical emission spectroscopy actinometry

    Institute of Scientific and Technical Information of China (English)

    Huang Song; Xin Yu; Ning Zhao-Yuan

    2005-01-01

    C4F8 plasma with the addition of H2 is generated by the inductively coupled plasma (ICP) method. The relative densities of CF, CF2, H and F radicals are determined by actinometric optical emission spectroscopy (AOES) as a function of the gas flow rate ratio R=H2/(H2+C4F8) at a pressure of 0.8 Pa and an input r.f. power of 400W, while that of HF is measured by quadrupole mass spectrometry (QMS). The results show that plasma activity increases firstly and then decreases with increasing R. As the gas flow rate ratio R changes from 0 to 0.625, relative densities of both CF and CF2 decrease, and the relative [CF] has a similar tendency as the calculated [CF], indicating that CF radicals are generated mainly by the electron impact dissociation of CF2 radicals. Production of HF is also discussed.

  10. Gas phase optical emission spectroscopy during remote plasma chemical vapour deposition of GaN and relation to the growth dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Corr, Cormac; Boswell, Rod [Space Plasma, Power and Propulsion Group, Plasma Research Laboratory, Research School of Physics and Engineering, Australian National University, Canberra 0200 (Australia); Carman, Robert [Physics Department, Macquarie University, North Ryde, Sydney, NSW 2109 (Australia)

    2011-02-02

    A remote plasma chemical vapour deposition (RPCVD) system for the growth of gallium nitride (GaN) thin films is investigated using optical emission spectroscopy (OES). The intensities of the various excited species in pure nitrogen as well as nitrogen/hydrogen plasmas are correlated with GaN film growth characteristics. We show a correlation between the plasma source spectrum, the downstream spectrum where trimethylgallium is introduced and the GaN film quality. In particular, we investigate the addition of hydrogen, which greatly affects the gas phase species and the GaN film characteristics. OES is demonstrated to be a valuable monitoring tool in a RPCVD system for optimization of GaN growth.

  11. Electron correlation energy of La sub x Sr sub 1 sub - sub x TiO sub 3 by high-resolution soft-X-ray emission spectroscopy

    CERN Document Server

    Higuchi, T; Tsukamoto, T; Harada, Y; Taguchi, Y; Tokura, Y; Shin, S

    2003-01-01

    The electronic structure of La sub x Sr sub 1 sub - sub x TiO sub 3 (x<=0.10) has been investigated by high-resolution soft-X-ray emission spectroscopy (SXES) spectra in the Ti 2p energy region. At the t sub 2 sub g -resonance SXES spectra, the d-d transition whose Raman shift is about 2.2 eV corresponds to the magnitude of the half intra-atomic Coulomb energy (U sub d sub d /2). The magnitude does not change in x<=0.10. This fact is consistent with the results obtained from the effective mass and the electronic specific heat.

  12. Highly polarized emission in spin resolved photoelectron spectroscopy of alpha-Fe(001)/GaAs(001)

    Energy Technology Data Exchange (ETDEWEB)

    Tobin, James; Yu, Sung Woo; Morton, Simon; Waddill, George; Thompson, Jamie; Neal, James; Spangenberg, Matthais; Shen, T.H.

    2009-05-19

    Highly spin-polarized sources of electrons, Integrated into device design, remain of great interest to the spintronic and magneto-electronic device community Here, the growth of Fe upon GaAs(001) has been studied with photoelectron spectroscopy (PES), including Spin Resolved PES. Despite evidence of atomic level disorder such as intermixing, an over-layer with the spectroscopic signature of alpha-Fe(001), with a bcc real space ordering, Is obtained The results will be discussed in light of the possibility of using such films as a spin-polarized source in device applications.

  13. Spectral and spatial resolution of the 12.8 micron Ne 2 emission from the galactic center. [astronomical spectroscopy/emission spectra, radio sources (astronomy)

    Science.gov (United States)

    Wollman, E. R.; Geballe, T. R.; Lacy, J. H.; Townes, C. H.; Rank, D. M.

    1975-01-01

    High-resolution spectra of the Ne II 12.8 micron fine-structure line in emission from the galactic center cloud Sgr A West show a line-center LSR radial velocity of + 75 + or - 20 km/sec. and a velocity dispersion of about 200 km/sec. The line has been observed with spectral resolution as high as 0.10/cm and spatial resolution as high as 8 sec. This appears to provide a direct measurement of conditions in the 45 sec. ionized region at the galactic center. The radial velocity and dispersion are more-or-less independent of position and indicate that events as recent as the last 4 million years have given the ionized gas a systematic motion with respect to the massive stellar component of material at the galactic center. An upper limit for the mass approximately equal to four million times the solar mass was obtained from the velocity distribution, with the mass located within 0.8 parsecs of the galactic center.

  14. Quantifying aflatoxins in peanuts using fluorescence spectroscopy coupled with multi-way methods: Resurrecting second-order advantage in excitation-emission matrices with rank overlap problem.

    Science.gov (United States)

    Sajjadi, S Maryam; Abdollahi, Hamid; Rahmanian, Reza; Bagheri, Leila

    2016-03-05

    A rapid, simple and inexpensive method using fluorescence spectroscopy coupled with multi-way methods for the determination of aflatoxins B1 and B2 in peanuts has been developed. In this method, aflatoxins are extracted with a mixture of water and methanol (90:10), and then monitored by fluorescence spectroscopy producing EEMs. Although the combination of EEMs and multi-way methods is commonly used to determine analytes in complex chemical systems with unknown interference(s), rank overlap problem in excitation and emission profiles may restrain the application of this strategy. If there is rank overlap in one mode, there are several three-way algorithms such as PARAFAC under some constraints that can resolve this kind of data successfully. However, the analysis of EEM data is impossible when some species have rank overlap in both modes because the information of the data matrix is equivalent to a zero-order data for that species, which is the case in our study. Aflatoxins B1 and B2 have the same shape of spectral profiles in both excitation and emission modes and we propose creating a third order data for each sample using solvent as a new additional selectivity mode. This third order data, in turn, converted to the second order data by augmentation, a fact which resurrects the second order advantage in original EEMs. The three-way data is constructed by stacking augmented data in the third way, and then analyzed by two powerful second order calibration methods (BLLS-RBL and PARAFAC) to quantify the analytes in four kinds of peanut samples. The results of both methods are in good agreement and reasonable recoveries are obtained.

  15. Quantifying aflatoxins in peanuts using fluorescence spectroscopy coupled with multi-way methods: Resurrecting second-order advantage in excitation-emission matrices with rank overlap problem

    Science.gov (United States)

    Sajjadi, S. Maryam; Abdollahi, Hamid; Rahmanian, Reza; Bagheri, Leila

    2016-03-01

    A rapid, simple and inexpensive method using fluorescence spectroscopy coupled with multi-way methods for the determination of aflatoxins B1 and B2 in peanuts has been developed. In this method, aflatoxins are extracted with a mixture of water and methanol (90:10), and then monitored by fluorescence spectroscopy producing EEMs. Although the combination of EEMs and multi-way methods is commonly used to determine analytes in complex chemical systems with unknown interference(s), rank overlap problem in excitation and emission profiles may restrain the application of this strategy. If there is rank overlap in one mode, there are several three-way algorithms such as PARAFAC under some constraints that can resolve this kind of data successfully. However, the analysis of EEM data is impossible when some species have rank overlap in both modes because the information of the data matrix is equivalent to a zero-order data for that species, which is the case in our study. Aflatoxins B1 and B2 have the same shape of spectral profiles in both excitation and emission modes and we propose creating a third order data for each sample using solvent as a new additional selectivity mode. This third order data, in turn, converted to the second order data by augmentation, a fact which resurrects the second order advantage in original EEMs. The three-way data is constructed by stacking augmented data in the third way, and then analyzed by two powerful second order calibration methods (BLLS-RBL and PARAFAC) to quantify the analytes in four kinds of peanut samples. The results of both methods are in good agreement and reasonable recoveries are obtained.

  16. Measurement of the hot spot electron temperature in NIF ICF implosions using Krypton x-ray emission spectroscopy

    Science.gov (United States)

    Ma, T.; Chen, H.; Patel, P. K.; Schneider, M.; Barrios, M.; Berzak Hopkins, L.; Casey, D.; Chung, H.-K.; Hammel, B.; Jarrott, C.; Nora, R.; Pak, A.; Scott, H.; Spears, B.; Weber, C.

    2015-11-01

    The inference of ion temperature from neutron spectral measurements in indirect-drive ICF implosions is known to be sensitive to non-thermal velocity distributions in the fuel. The electron temperature (Te) inferred from dopant line ratios should not be sensitive to these bulk motions and hence may be a better measure of the thermal temperature of the hot spot. Here we describe a series of experiments to be conducted on the NIF where a small concentration of a mid-Z dopant (Krypton) is added to the fuel gas. The x-ray spectra is measured and the electron temperature is inferred from Kr line ratios. We also quantify the level of radiative cooling in the hot spot due to this mid-Z dopant. These experiments represent the first direct measurement of hot spot Te using spectroscopy, and we will describe the considerations for applying x-ray spectroscopy in such dense and non-uniform hot spots. This work performed under the auspices of U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344.

  17. X-ray absorption and emission spectroscopy of Cr(III) (hydr)oxides: analysis of the K-pre-edge region.

    Science.gov (United States)

    Frommer, Jakob; Nachtegaal, Maarten; Czekaj, Izabela; Weng, Tsu-Chien; Kretzschmar, Ruben

    2009-11-05

    Pre-edge spectral features below the main X-ray absorption K-edge of transition metals show a pronounced chemical sensitivity and are promising sources of structural information. Nevertheless, the use of pre-edge analysis in applied research is limited because of the lack of definite theoretical peak-assignments. The aim of this study was to determine the factors affecting the chromium K-pre-edge features in trivalent chromium-bearing oxides and oxyhydroxides. The selected phases varied in the degree of octahedral polymerization and the degree of iron-for-chromium substitution in the crystal structure. We investigated the pre-edge fine structure by means of high-energy-resolution fluorescence detected X-ray absorption spectroscopy and by 1s2p resonant X-ray emission spectroscopy. Multiplet theory and full multiple-scattering calculations were used to analyze the experimental data. We show that the chromium K-pre-edge contains localized and nonlocalized transitions. Contributions arising from nonlocalized metal-metal transitions are sensitive to the nearest metal type and to the linkage mode between neighboring metal octahedra. Analyzing these transitions opens up new opportunities for investigating the local coordination environment of chromium in poorly ordered solids of environmental relevance.

  18. Emission and absorption spectroscopy study of Ar excited states in 13.56 MHz argon plasma operating at sub-atmospheric to atmospheric pressure

    Energy Technology Data Exchange (ETDEWEB)

    Li, L. [Department of Applied Physics, Research Unit Plasma Technology, Ghent University, Jozef Plateaustraat 22, Ghent B-9000 (Belgium); Nikiforov, A., E-mail: anton.nikiforov@ugent.be [Department of Applied Physics, Research Unit Plasma Technology, Ghent University, Jozef Plateaustraat 22, Ghent B-9000 (Belgium); Institute of Solution Chemistry of the Russian Academy of Science, Academicheskaya St., 1, Ivanovo, 153045 (Russian Federation); Britun, N. [Chimie des Interactions Plasma-Surface (ChIPS), CIRMAP, Universite de Mons, 23 Place du Parc, B-7000 Mons (Belgium); Snyders, R. [Chimie des Interactions Plasma-Surface (ChIPS), CIRMAP, Universite de Mons, 23 Place du Parc, B-7000 Mons (Belgium); Materia Nova Research Centre, Parc Initialis, B-7000 Mons (Belgium); Leys, C. [Department of Applied Physics, Research Unit Plasma Technology, Ghent University, Jozef Plateaustraat 22, Ghent B-9000 (Belgium)

    2015-05-01

    The densities of metastable and resonant states of Ar atoms are measured in high pressure Ar radio frequency discharge. Resonant absorption spectroscopy for the case of a low pressure spectral lamp and high-pressure plasma absorption lines is implemented for this purpose. The necessary generalizations for the high-pressure resonant absorption method are given. Absolute density of Ar 1s levels obtained at different RF input power and operating pressures are of the order of 10{sup 11} cm{sup −3}, which is in a good agreement with those reported in the literature. The population distribution on the Ar 2p (excited) levels, obtained from the optical emission spectroscopy, reveals strong deviation from thermal equilibrium for these levels in the high-pressure case. The generation of the Ar excited states in the studied discharges is compared to the previously reported results. - Highlights: • Strong non-equilibrium distribution of Ar 2p levels is observed. • The absolute number density of non-radiative Ar 1s states is determined by the easier and low cost spectral-lamp absorption method. • The modified absorption theory of Mitchell and Zemanski was used to obtain the absolute number density of Ar 1s states at high pressure. • The developed RF source with 5 cm long gap can be a possible alternative to micro-plasma working in Ar at atmospheric pressure.

  19. Measurement of Electron Density Using the Multipole Resonance Probe, Langmuir Probe and Optical Emission Spectroscopy in Low Pressure Plasmas with Different Electron Energy Distribution Functions

    Science.gov (United States)

    Oberberg, Moritz; Bibinov, Nikita; Ries, Stefan; Awakowicz, Peter; Institute of Electrical Engineering; Plasma Technology Team

    2016-09-01

    In recently publication, the young diagnostic tool Multipole Resonance Probe (MRP) for electron density measurements was introduced. It is based on active plasma resonance spectroscopy (