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Sample records for trace element determination

  1. Determination of Trace Elements in Thai Cereal

    International Nuclear Information System (INIS)

    Permnamtip, Vorapot; Busamongkol, Arporn; Laoharojanaphand, Sirinart; Chaiyasith, Suwan

    2007-08-01

    Full text: Trace elements were analyzed in Thai cereal, e.g. rice and bean, by using neutron activation analysis (NAA). The selected cereals are major food items for Thai population. The data obtained from this work will be useful for nutrition and safety consumption of Thai cereal. Trace elements verified include Al, As, Br, Ca, Cd, Cl, Cr, Cu, Fe, I, K, Mg, Mn, Mo, Se, Sn, V and Zn. It was found that Al, As, Br, Cl, Cu, Fe, Mn, Zn, Ca, K and Mg are presented in the range of 2.2 to 35.7, 0.15 to 0.21, 0.44 to 13.5, 55.6 to 640.3, 16.3 to 16.5, 158.9 to 161.1, 12.2 to 55.7, 8.2 to 58.1 (g/g (ppm) , 0.02 to 0.28, 0.09 to 1.99 and 0.03 to 0.26 %, respectively. For Cd, Cr, I, Mo, Se, Sn and V were not found in sample because the concentrations were lower than detection limit. Precision and accuracy were determined by analyzing standard reference materials: NIST 1568a, NIST 8704, ACSP DORM-1, NIES No.9 and NMIJ 7302 to a

  2. INAA Application for Trace Element Determination in Biological Reference Material

    Science.gov (United States)

    Atmodjo, D. P. D.; Kurniawati, S.; Lestiani, D. D.; Adventini, N.

    2017-06-01

    Trace element determination in biological samples is often used in the study of health and toxicology. Determination change to its essentiality and toxicity of trace element require an accurate determination method, which implies that a good Quality Control (QC) procedure should be performed. In this study, QC for trace element determination in biological samples was applied by analyzing the Standard Reference Material (SRM) Bovine muscle 8414 NIST using Instrumental Neutron Activation Analysis (INAA). Three selected trace element such as Fe, Zn, and Se were determined. Accuracy of the elements showed as %recovery and precision as %coefficient of variance (%CV). The result showed that %recovery of Fe, Zn, and Se were in the range between 99.4-107%, 92.7-103%, and 91.9-112%, respectively, whereas %CV were 2.92, 3.70, and 5.37%, respectively. These results showed that INAA method is precise and accurate for trace element determination in biological matrices.

  3. Application of trace element analysis to determine trace element concentrations in the field of medicine

    International Nuclear Information System (INIS)

    Kasperek, K.; Feinendegen, L.E.

    1976-01-01

    Applied trace elements research in medicine requires a sensitive and efficient technique of trace elements analysis such as, e.g., neutron activation analysis. Essential trace elements act as stabilisators (iron in haem), structural elements (silicium in fibrous tissue), in hormones (iodine in thyroid hormone), in vitamins (cobalt in vitamin B 12), and in enzymes. Most of the essential trace elements act as coenzymes or in coenzymes or directly as metabolic catalysators. For example, selenium deficiency in PKU and maple syrup patients receiving dietary treatment can be detected by determining the selenium content of the serum, while low selenium values in the whole blood indicate liver cirrhosis. Acrodermatitis enteropathica can be diagnosed by determinig zinc in the serum, and pancreatic insufficiency by determining zinc in the pancreatic juice. Zinc also plays a part in disturbances of growth, in the healing of wounds, and in the insulin metabolism. Cobalt is important in some types of anaemia and in myocardiopathies. Trace elements are also necessary in the treatment of diseases, e.g. iron cobalt in some types of anaemia, and zinc in the delayed healing of wounds in the postoperative phase and in acrodermatitis enteropathica. Chromium is now being tested for the treatment of diabetes mellitus, and fluorides may be of interest in the treatment of osteoporosis. Finally, trace elements are important in the aetiology of acute poisoning, in nutrition, and in environmental protection. (orig./AK) [de

  4. Application of trace element analysis to determine trace element concentrations in the field of medicine. [Neutrons

    Energy Technology Data Exchange (ETDEWEB)

    Kasperek, K; Feinendegen, L E

    1976-01-01

    Applied trace elements research in medicine requires a sensitive and efficient technique of trace elements analysis, such as neutron activation analysis. Essential trace elements act as stabilizators (iron in haem), structural elements (silicon in fibrous tissue), in hormones (iodine in thyroid hormone), in vitamins (cobalt in vitamin B 12), and in enzymes. Most of the essential trace elements act as coenzymes or in coenzymes or directly as metabolic catalyzers. For example, selenium deficiency in PKU and maple syrup patients receiving dietary treatment can be detected by determining the selenium content of the serum, while low selenium values in the whole blood indicate liver cirrhosis. Acrodermatitis enteropathica can be diagnosed by determinig zinc in the serum, and pancreatic insufficiency by determining zinc in the pancreatic juice. Zinc also plays a part in disturbances of growth, in the healing of wounds, and in the insulin metabolism. Cobalt is important in some types of anaemia and in myocardiopathies. Trace elements are also necessary in the treatment of diseases, e.g. iron cobalt in some types of anaemia, and zinc in the delayed healing of wounds in the postoperative phase and in acrodermatitis enteropathica. Chromium is now being tested for the treatment of diabetes mellitus, and fluorides may be of interest in the treatment of osteoporosis. Finally, trace elements are important in the aetiology of acute poisoning, in nutrition, and in environmental protection.

  5. Trace elements determination in human hair

    International Nuclear Information System (INIS)

    Carrion, Jose

    1995-01-01

    Concentrations of Cu, Zn, Pb, Mg, Ca, Na, K, Mn, Cr, Ni, Co, V, Cd and Al, in human hair sampled from 23 young men during 24 months were determined by atomic absorption spectroscopy. Additional determination of mercury and volatile elements were made by using accessory MHS-10. Statistical treatment of data is presented for each person and element. The pre-treatment of hair carried out with an organic solvent to remove the superficial pollutants is explained. (The author)

  6. Determination of trace elements in airborne particulate matter. Pt. 2

    International Nuclear Information System (INIS)

    Pamuk, F.; Kahraman, N.; Kut, D.

    1975-04-01

    Several trace elements are being introduced into the atmosphere from various sources. Since many of the trace elements are highly toxic, the concentrations of them should be measured and controlled continuously for public health. Concentrations of trace elements have been determined in air samples collected from seven different districts of Ankara by the use of instrumental neutron activation analysis and atomic absorption spectrophotometer. (Pamuk, F.; Kahraman, N.; Kut, D.)

  7. The separation and determination of trace elements in iron ore

    International Nuclear Information System (INIS)

    Jones, E.A.

    1977-01-01

    The separation, concentration, and determination of trace elements in iron ores are described. After the sample has been dissolved, the iron is separated by liquid-liquid extraction with a liquid cation-exchanger, di-(2-ethylhexyl) phosphoric acid. The trace elements aluminium, cadmium, calcium, chromium, cobalt, copper, lead, magnesium, manganese, mercury, potassium, sodium, vanadium, and zinc are determined in the aqueous phase by atomic-absorption spectrophotometry

  8. Determination of trace elements in electronic materials by NAA

    International Nuclear Information System (INIS)

    Kobayashi, Kenji

    1986-01-01

    Trace amounts of elements in electronic materials were determined by instrumental neutron activation analysis (INAA), re-activation analysis and substoichiometric radioactivation analysis using gamma-ray spectrometry. Ten elements (Cr, Cu, Fe, Zn, Co, Eu, Ir, Sb, Sc, Tb) in gallium arsenide single crystal were determined by INAA and substoichiometric radioactivation analysis. Trace level of chromium (10 13 atoms/cm 3 ) and zinc (10 14 atoms/cm 3 ) in gallium arsenide single crystal were determined by INAA. The chromium concentrations in horizontal Bridgmangrown semi-insulating gallium arsenide ingot were ranged from 1.2 x 10 16 atoms/cm 3 at seed end to 3.5 x 10 16 atoms/cm 3 at tail end. The trace determinations of iron (10 14 atoms/cm 3 ) and copper (10 14 atoms/cm 3 ) in silicon, gallium arsenide and indium phoshide single crystals were carried out by substoichiometric radioactivation analysis. The reactivation analysis for the multielement determination of indium phosphide single crystal was carried out and nineteen elements were determined simultaneously by gamma-ray spectrometry. Eleven elements (Ag, As, Br, Co, Cr, Fe, K, Mn, Sb, Sc, Zn) in four NIES standard reference materials (Pond Sediment, Chlorella, Mussel and Tea Leaves) and seven elements (Co, Cr, Eu, Fe, Sc, Tb, Yb) in two NBS glasses (SRM-615 and SRM-613) were determined by INAA and substoichiometric radioactivation analysis and the analytical results obtained by the methods were in good agreement with certified values by NIES and NBS. (author)

  9. Determination of trace elements in urban airborne particulates (PM ...

    African Journals Online (AJOL)

    Assessment of the air quality in Newcastle upon Tyne, UK was performed by determining the trace element content in airborne particulates (PM10). Samples were collected over a 12 month period (March 2011 to April 2012) using two high volume air sampler provided with a PM10 size selective inlet. The concentrations of ...

  10. ICP-AES determination of trace elements in carbon steel

    International Nuclear Information System (INIS)

    Sengupta, Arijit; Rajeswari, B.; Kadam, R.M.; Babu, Y.; Godbole, S.V.

    2010-01-01

    Full text: Carbon steel, a combination of the elements iron and carbon, can be classified into four types as mild, medium, high and very high depending on the carbon content which varies from 0.05% to 2.1%. Carbon steel of different types finds application in medical devices, razor blades, cutlery and spring. In the nuclear industry, it is used in feeder pipes in the reactor. A strict quality control measure is required to monitor the trace elements, which have deleterious effects on the mechanical properties of the carbon steel. Thus, it becomes imperative to check the purity of carbon steel as a quality control measure before it is used in feeder pipes in the reactor. Several methods have been reported in literature for trace elemental determination in high purity iron. Some of these include neutron activation analysis, atomic absorption spectrometry and atomic emission spectrometry. Inductively coupled plasma atomic emission spectrometry (ICP-AES) is widely recognized as a sensitive technique for the determination of trace elements in various matrices, its major advantages being good accuracy and precision, high sensitivity, multi-element capability, large linear dynamic range and relative freedom from matrix effects. The present study mainly deals with the direct determination of trace elements in carbon steel using ICP-AES. An axially viewing ICP spectrometer having a polychromator with 35 fixed analytical channels and limited sequential facility to select any analytical line within 2.2 nm of a polychromator line was used in these studies. Iron, which forms one of the main constituents of carbon steel, has a multi electronic configuration with line rich emission spectrum and, therefore, tends to interfere in the determination of trace impurities in carbon steel matrix. Spectral interference in ICP-AES can be seriously detrimental to the accuracy and reliability of trace element determinations, particularly when they are performed in the presence of high

  11. Trace element impurity determination in aspirin tablets by INAA

    International Nuclear Information System (INIS)

    Miyoshi, E.K.; Saiki, M.

    2009-01-01

    Instrumental neutron activation analysis (INAA) was applied to assess trace element concentrations in six samples of aspirin tablets acquired in Sao Paulo city, Brazil. Concentrations of the elements Br, Ca, Co, Cr, Fe, K, La, Na, Sc and Zn were determined. Comparisons were made between the results obtained with published data for aspirins from foreign countries. Certified reference materials, INCT-MPH-2 Mixed Polish Herbs were analyzed for quality control of the analytical results. (author)

  12. Determination of trace elements in chicken feeds in Khartoum state

    International Nuclear Information System (INIS)

    Hassan, Salma Yahya Mohammed

    2017-03-01

    Trace elements are very important for chicken because thy contribute in biochemical processes required for normal growth, development and formation of the eggshell. The deficiency or the elevation of these trace elements may affect the normal physiological activity and biochemical process of their bodies. In this study the concentrations of trace elements in chicken feed samples were determined by X RF spectrometry. The results showed that there were 9 trace elements in sample ( K, Ca Mn, Fe Cu Zn, Pb, Rb, Sr) the mean concentration were K ( 2.12 x 10 4 ), Ca (2.22x10 4 ), Mn (48.1). Fe (191), Cu(9.81), Zn (24.6), Pb (1.63), Rb (7.79), Sr(4.09) ppm. Comparing the trace elements concentrations obtained in this study with the recommended values showed that some of them e.g Mn, Cu, Zn, Fe were found higher concentration than the recommended values, which stipulated by national research council NRC European Union. While lead concentration was in the permissible limit (5mg/kg). However, the statistical Alan's revealed than there were no significant difference between all concentrations of trace elements in the two types of chicken feeds i.e layer and broiler. The pearson correlation test displayed a strong correlation between K-Rb (0.885), Mn-Zn (0.874). The negative correlation between Mn-Rb (0.680), K-Mn (0.6000), K-Ca (0.565), Zn-Rb (-0.541). Ca-Rb (0.458) were found . Further investigations were performed using the principal component analysis (PCA) which involved the extraction of principal factor to study the total variance in the feed samples in terms of the trace elements concentrations in each. The obtained results revealed that the first principal component have a positive correlation with the elements Ca, Mn, Pb, and Zn, while K and Rb showed negative correlation with it. Similarly, the second principal compound showed positive correlation with the elements Mn, PB and Zn, while Ca and Sr showed negative, on the perth hand the third component was found to

  13. [Determination and correlation analysis of trace elements in Boletus tomentipes].

    Science.gov (United States)

    Li, Tao; Wang, Yuan-zhong; Zhang, Ji; Zhao, Yan-li; Liu, Hong-gao

    2011-07-01

    The contents of eleven trace elements in Boletus tomentipes were determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES). The results showed that the fruiting bodies of B. tomentipes were very rich in Mg and Fe (>100 mg x kg(-1)) and rich in Mn, Zn and Cu (>10 mg x kg(-1)). Cr, Pb, Ni, Cd, and As were relatively minor contents (0.1-10.0 mg x kg(-1)) of this species, while Hg occurred at the smallest content (< 0.1 mg x kg(-1)). Among the determined 11 trace elements, Zn-Cu had significantly positive correlation (r = 0.659, P < 0.05), whereas, Hg-As, Ni-Fe, and Zn-Mg had significantly negative correlation (r = -0.672, -0.610, -0.617, P < 0.05). This paper presented the trace elements properties of B. tomentipes, and is expected to be useful for exploitation and quality evaluation of this species.

  14. New trace element determinations in the fingernails of ALS patients

    Energy Technology Data Exchange (ETDEWEB)

    Van Dalsem, D.J.; Ehmann, W.D. [Univ. of Kentucky, Lexington, KY (United States); Robinson, L. [Oak Ridge National Laboratory, TN (United States)

    1996-12-31

    Amyotrophic lateral sclerosis (ALS) afflicts 2 of every 100,000 people in the United States each year. A well-known example of ALS today is Stephen Hawking. He is a theoretical physicist, the author of A Brief History of Time, and is virtually immobilized by ALS. Diseases that cause progressive paralysis because of motor neuron degeneration in the central nervous system are termed motor neuron disorders (MND). Amyotrophic lateral sclerosis is a common form of MND. Pain-free, progressive muscular weakness is the most common clinical symptom. There is chronic weakness with atrophy of the affected muscles by the time the disease is diagnosed. Atrophy eventually results in wheelchair confinement and then only bed without the ability to speak or swallow. Death often occurs as a result of respiratory problems. Unlike other neurodegenerative diseases, in ALS the patient`s bladder and bowel control, eye movement, and mental faculties are preserved. The question today is whether or not certain trace elements are involved in the etiology or pathogenesis of ALS. A collaborative study was undertaken by the University of Kentucky and Oak Ridge National Laboratory (ORNL) using neutron activation analysis (NAA) to study trace element concentrations in ALS patients fingernails to determine if there existed statistically significant imbalances.

  15. Determination of refractory trace elements in Chinese meteorites by RNAA

    International Nuclear Information System (INIS)

    Kraehenbuehl, U.; Burger, M.

    1989-01-01

    Some refractory trace elements are important target elements for spallation reactions in meteorites. These elements also serve to characterize the investigated meteorites. The elements Ti, Y, Zr, Hf, W and Ta were measured after radiochemical separation in chondrites from China. After acid digestion of the irradiated samples, the group separations were obtained by precipitation reactions. The necessary radiochemical purification of the pure β emitter Y was realized on a Lewatite OC 1026 column. For all the other elements discrete gamma radiation was measured. (orig.)

  16. Trace elements in natural drugs determined by INAA

    International Nuclear Information System (INIS)

    Chen Kehshaw; Tseng Chialiang; Lin Tehsien

    1993-01-01

    Natural drugs are widely used for diuretic, phlegm elimination and stomach invigoration purposes. Seventy-five of the most common remedies used by Chinese people have been subjected to trace element survey analysis by instrumental neutron activation. Within this large number of different natural products, fourteen trace elements (K, Sc, Cr, Fe, Co, Zn, Br, Rb, Cs, La, Sm, Eu, Au and Th) are commonly detected. Among these elements, Fe had the highest concentration followed by Zn, and Rb, Sm, Eu and Au were found to have the lowest concentrations. Although the three groups of natural drugs exhibit a widely different therapeutic action, the concentration ranges of the fourteen elements were very similar. While this suggests no apparent specific role for the trace elements in the drug function, parallels are drawn between the known drug related functions of Rb, Zn, Br, Fe, Co and K and the levels of elements found in the natural drugs. It is concluded that the various natural drugs also provide human benefits through supplements of essential elements such as Fe, Zn, Cr, Sc, Rb and Co. (author) 13 refs.; 5 tabs

  17. Determination of trace elements by resonant ionization mass spectrometry (RIMS)

    International Nuclear Information System (INIS)

    Ruster, W.; Ames, F.; Rehklau, D.; Mang, M.; Muehleck, C.; Rimke, H.; Sattelberger, P.; Herrmann, G.; Trautmann, N.; Kluge, H.J.; Otten, E.W.

    1988-01-01

    A resonant ionization mass spectrometer has been developed as an analytical tool for the detection of trace elements, especially of plutonium and other radionuclides. The sample, deposited on a rhenium filament, is evaporated by electrical heating and the atoms of the element under investigation are selectively ionized by laser light delivered from three dye lasers pumped by a copper vapour laser. The resulting photoions are detected in a time-of-flight spectrometer with a channelplate detector. For plutonium a mass resolution of M/ΔM=1500 was obtained and an overall detection efficiency of 4x10 -6 was determined for stepwise excitation and ionization via autoionizing states. With a laser light bandwidth of 3-5 GHz neighbouring isotopes could be suppressed by a factor of 20 due to isotope shifts in the excitation transitions. The isotope composition of synthetic samples was measured and good agreement was found with mass spectroscopic results. The influence of the hyperfine structure on the isotope ratios is discussed. (orig.)

  18. Determination of toxic trace elements in body fluid reference samples

    International Nuclear Information System (INIS)

    Gills, T.E.; McClendon, L.T.; Maienthal, E.J.; Becker, D.A.; Durst, R.A.; LaFleur, P.D.

    1974-01-01

    The measurement of elemental concentration in body fluids has been widely used to give indication of exposures to certain toxic materials and/or a measure of body burden. To understand fully the toxicological effect of these trace elements on our physiological system, meaningful analytical data are required along with accurate standards or reference samples. The National Bureau of Standards has prepared for the National Institute for Occupational Safety and Health (NIOSH) a number of reference samples containing selected toxic trace elements in body fluids. The reference samples produced include mercury in urine at three concentration levels, five elements (Se, Cu, As, Ni and Cr) in freeze-dried urine at two levels, fluorine in freeze-dried urine at two levels and lead in blood at two concentration levels. These reference samples have been found to be extremely useful for the evaluation of field and laboratory analytical methods for the analysis of toxic trace elements. In particular the use of at least two calibration points (i.e., ''normal'' and ''elevated'' levels) for a given matrix provides a more positive calibration for most analytical techniques over the range of interest for occupational toxicological levels of exposure. (U.S.)

  19. Determining trace element in hair of children with mental retardation

    International Nuclear Information System (INIS)

    Wang Zhilan; Gu Bomei; Jia Meixiang

    1992-01-01

    Seven trace elements in the hair come from 29 mental retardation children and 29 normal children have been analysed by INAA and XRF. There are significant differences for Fe and Sc between the two groups. The average value of Pb in the hair of the mental retardation children is higher than that of the normal children. Although Zn is very important for children growing, there is no significant difference between two children groups

  20. Concentration of 24 Trace Elements in Human Heart Tissue Determined by Neutron Activation Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Wester, P O

    1964-06-15

    By means of neutron-activation analysis, human heart tissue from autopsy of 20 victims of traumatic accidents has been investigated with respect to the concentration of 24 different trace elements. A recently developed ion-exchange technique combined with gamma spectrometry has been used, which permits simultaneous determination of a large number of trace elements. The following trace elements have been determined quantitatively: Ag, As, Au, Ba, Br; Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Hg, La, Mo, Pt, Rb, Sb, Se, Se, Sm, Zn, W. In some heart samples, Hf and Os were determined qualitatively. The mean and standard deviation are given for the elements Cu, Fe, Se and Zn, Since none of the other quantitatively determined trace elements were normally distributed, the median is given as the central value. When possible, comparisons with values from other investigations have been made. No marked differences in the trace-element concentrations with age or sex could be detected.

  1. Concentration of 24 Trace Elements in Human Heart Tissue Determined by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Wester, P.O.

    1964-06-01

    By means of neutron-activation analysis, human heart tissue from autopsy of 20 victims of traumatic accidents has been investigated with respect to the concentration of 24 different trace elements. A recently developed ion-exchange technique combined with gamma spectrometry has been used, which permits simultaneous determination of a large number of trace elements. The following trace elements have been determined quantitatively: Ag, As, Au, Ba, Br; Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Hg, La, Mo, Pt, Rb, Sb, Se, Se, Sm, Zn, W. In some heart samples, Hf and Os were determined qualitatively. The mean and standard deviation are given for the elements Cu, Fe, Se and Zn, Since none of the other quantitatively determined trace elements were normally distributed, the median is given as the central value. When possible, comparisons with values from other investigations have been made. No marked differences in the trace-element concentrations with age or sex could be detected

  2. Determination of trace elements in KRISS biological CRMs by INAA

    International Nuclear Information System (INIS)

    Cho, Kyung Haeng; Park, Kwang Won; Zeisler, Rolf

    2005-01-01

    Two biological Certified Reference Materials (CRMs), KRISS 108-04-001 (oyster tissue) and 108-05-001 (water dropwort stem), were prepared by Korea Research Institute of Standards and Science (KRISS) during FY '01. The certified values of these materials had been determined by Isotope Dilution Mass Spectrometry (IDMS) for six elements (Cd, Cr, Cu, Fe, Pb and Zn). Additional analytical works are now progressing to certify the concentrations of a number of the environmental and nutrimental elements in these CRMs. The certified values in a CRM are usually determined by using a single primary method with confirmation by other method(s) or using two independent critically-evaluated methods. Instrumental Neutron Activation Analysis (INAA) plays an important role in determination of certified values. INAA procedure was used in determination of 20 elements in these two biological CRMs to acquire the concentration information and the results were compared with KRISS certified values

  3. Non-destructive determination of trace elements. Final progress report

    International Nuclear Information System (INIS)

    Anderson, D.L.; Gordon, G.E.; Zoller, W.H.; Walters, W.B.; Lindstrom, R.M.

    1984-05-01

    In the course of this project we have successfully designed, built, and tested the first neutron beam facility dedicated to routine multielement neutron capture prompt-γ activation analysis (PGAA). This technique is capable of accurately measuring concentrations of up to 20 elements in a number of sample types, and is an extremely valuable complement to instrumental neutron activation analysis (INAA) and other analytical methods. We have found PGAA to have some major advantages over INAA: (1) the sample is subjected to neutron fluxes about five orders of magnitude less than in PGAA, with essentially no radiation or heating damage; (2) as the data are taken during sample irradiation, analyses can be performed immediately instead of waiting up to four weeks as in INAA; (3) it is capable of measuring all major elements, except oxygen, in many samples, including H, C, N, and Si, which cannot be done by INAA; and (4) it is especially sensitive for the trace elements B, Cd, Sm and Gd. In addition, we have characterized the overall capabilities of PGAA and the corrections necessary to make it an extremely accurate technique. We have applied PGAA in a number of studies in which it has proved to be extremely valuable and, at times, even providing crucial information that other techniques were incapable of supplying. 1 fig., 6 tabs

  4. New trace element determinations in the fingernails of ALS patients

    Energy Technology Data Exchange (ETDEWEB)

    Van Dalsem, D.J.; Robinson, L. [Oak Ridge National Lab., TN (United States); Ehmann, W.D. [Kentucky Univ., Lexington, KY (United States). Dept. of Chemistry

    1996-02-01

    ORNL`s High Flux Isotope Reactor was used in a neutron activation analysis experiment to determine selected elemental composition of fingernails from patients afflicted with amyotrophic lateral sclerosis (AL). While no statistical difference were found in aluminium a suggestive difference was observed for copper concentrations.

  5. New trace element determinations in the fingernails of ALS patients

    International Nuclear Information System (INIS)

    Van Dalsem, D.J.; Robinson, L.; Ehmann, W.D.

    1996-01-01

    ORNL's High Flux Isotope Reactor was used in a neutron activation analysis experiment to determine selected elemental composition of fingernails from patients afflicted with amyotrophic lateral sclerosis (AL). While no statistical difference were found in aluminium a suggestive difference was observed for copper concentrations

  6. Determination of trace elements in the human substantia nigra

    Energy Technology Data Exchange (ETDEWEB)

    Morawski, M. [Paul-Flechsig-Institut fuer Hirnforschung, Universitaet Leipzig, Jahnallee 59, 04109 Leipzig (Germany)]. E-mail: morm@medizin.uni-leipzig.de; Meinecke, Ch. [Fakultaet fuer Physik und Geowissenschaften, Universitaet Leipzig, Linnestrasse 5, 04105 Leipzig (Germany); Reinert, T. [Fakultaet fuer Physik und Geowissenschaften, Universitaet Leipzig, Linnestrasse 5, 04105 Leipzig (Germany); Doerffel, A.C. [Paul-Flechsig-Institut fuer Hirnforschung, Universitaet Leipzig, Jahnallee 59, 04109 Leipzig (Germany); Riederer, P. [Klin. Neurochemie, Abt. Psychiatrie, Universitaet Wuerzburg, Fuechsleinstrasse 15, 97080 Wuerzburg (Germany); Arendt, T. [Paul-Flechsig-Institut fuer Hirnforschung, Universitaet Leipzig, Jahnallee 59, 04109 Leipzig (Germany); Butz, T. [Fakultaet fuer Physik und Geowissenschaften, Universitaet Leipzig, Linnestrasse 5, 04105 Leipzig (Germany)

    2005-04-01

    'The gain in brain is mainly in the stain' was long time a key sentence for research in neurodegenerative disease. However, for a quantification of the element concentrations (especially iron) in brain tissue, standard staining methods are insufficient. Advanced physical methods allow a quantitative elemental analysis of brain tissue. The sophisticated ion beam analysis provides a quantitative determination of elemental concentrations with a subcellular spatial resolution using a scanning proton beam focussed down to below 1 {mu}m that induces characteristic X-rays in the specimen (PIXE - particle induced X-ray emission). Histochemical and biochemical determinations of total iron content in brain regions from idiopathic Parkinson's disease have demonstrated an increase of iron in parkinsonian substantia nigra pars compacta but not in the pars reticulata, however without a clear cellular classification. For the first time, we have differentially investigated the intra- and extraneuronal elemental concentrations (especially iron) of the human substantia nigra pars compacta versus pars reticulata with detection limits in the range of 50 {mu}mol/l. Thus, we could compare the neuronal iron concentration in human brain sections of healthy and parkinsonian brain tissue. Clear differences in the iron concentration and distribution could be disclosed. Additionally, we could show in situ that the increased intraneuronal iron content is linked to neuromelanin.

  7. Report on intercomparison A-13 of the determination of trace elements in freeze dried animal blood

    International Nuclear Information System (INIS)

    Pszonicki, L.; Hanna, A.N.; Suschny, O.

    1983-03-01

    This document deals with the comparative evaluation of the analytical data on the trace elements in beef blood obtained by 38 laboratories in 23 countries. The evaluations were based on 799 laboratory mean values of concentration of 41 elements. It was one of the series of IAEA intercomparisons on the determination of trace elements in animal materials. It was organized for the purpose of assisting the participating laboratories to check the accuracy of their work and to prepare a new reference material

  8. Quantitative determination of minor and trace elements in rocks and soils by spark source mass spectrometry

    International Nuclear Information System (INIS)

    Ure, A.M.; Bacon, J.R.

    1978-01-01

    Experimental details are given of the quantitative determination of minor and trace elements in rocks and soils by spark source mass spectrometry. The effects of interfering species, and corrections that can be applied, are discussed. (U.K.)

  9. Determination of trace elements in cockle Anadara Granosa L. using INAA

    International Nuclear Information System (INIS)

    Ibrahim, Noorddin

    1994-01-01

    This study determines the trace metal content in Anadara Granosa L., a popular seafood amongst South-East-Asians. Using the technique of instrumental neutron activation analysis (INAA) identification has been made of the presence of 17 trace metals including elements which are classified as toxic (As, Br, Cs) and those which are rare-earths (Eu, Ce, Lu, Tb, Yb). (author)

  10. PIXE determination of essential trace elements in some traditional Chinese medicines

    International Nuclear Information System (INIS)

    Xiao, L.; Qin, J.F.

    1990-01-01

    The essential trace elements in 30 traditional Chinese medicines, (24 tonics and 6 nontonics) were determined by proton-induced X-ray emission. The authors' previous suggestion that traditional Chinese medicines may be classified by the order of magnitude of their essential trace elements, thus indicating their pharmacological effects, is not justified. The pharmacological effect of a trace element or its essentiality may be dependent on some ligand that can be chelated with it. A nonlinear mapping algorithm, however, shows that the 30 traditional Chinese medicines are nearly separated into two groups, indicating their tonic or nontonic pharmacological effects

  11. Determination of trace elements in maifanite by outer cover electrode atomic emission spectrometry

    Institute of Scientific and Technical Information of China (English)

    LI Jianqiang; LU Yiqiang; JIANG Wei

    2005-01-01

    Maifanite is a nature medicinal stone used in many fields for long time. The research on it showed that there are many trace elements in maifanite. In this paper, 36 trace elements in maifanite were determined by outer cover electrode atomic emission spectrometry, and the determination conditions were studied systematically. The results show that the concentrafions of elements, which are beneficial to human health, are higher, and the elements harmful to people health such as As, Cd, Hg, Cr, and Pb are tiny in maifanite. The precision and the accuracy were also discussed.

  12. Characterization of prehistoric pottery from the Tremiti Isles by trace elements determination

    International Nuclear Information System (INIS)

    Brandone, A.; Fumo, P.; Giacco, M.; Oddone, M.; Riganti, V.; Baldi, M

    1993-01-01

    The potteries found on the Tremiti Isles (Italy, Adriatic Sea) have been characterized through their trace elements content. The goal of the work was to find out the number of ore deposits that supplied the clay used to manufacture the pottery. Neutron activation analysis has been employed for trace elements content determinations; the results have been statistically evaluated, clusterized and discussed. (author) 13 refs.; 1 fig.; 3 tabs

  13. Accuracy of trace element determinations in alternate fuels

    Science.gov (United States)

    Greenbauer-Seng, L. A.

    1980-01-01

    A review of the techniques used at Lewis Research Center (LeRC) in trace metals analysis is presented, including the results of Atomic Absorption Spectrometry and DC Arc Emission Spectrometry of blank levels and recovery experiments for several metals. The design of an Interlaboratory Study conducted by LeRC is presented. Several factors were investigated, including: laboratory, analytical technique, fuel type, concentration, and ashing additive. Conclusions drawn from the statistical analysis will help direct research efforts toward those areas most responsible for the poor interlaboratory analytical results.

  14. Determination of trace elements in drinking tea by various analytical techniques

    International Nuclear Information System (INIS)

    Wang Chufang; Ke Chenghsiung; Yang Jenqyann

    1993-01-01

    Tea has been one of the most popular simulating beverages which is both heavily produced and consumed in Taiwan. The determination of minor or trace elements in drinking tea and tea leaves is therefore important for estimating the daily intake of Taiwanese considered as a safety indicator. In order to accurately and precisely determine the concentrations of trace elements in samples, several analytical methods such as AAS, NAA and ICP-AES are suggested. This paper attempts to utilize all three methods to determine the concentrations of minor or trace elements in different types of tea leaves and the extracts percolated from them. The influence of fermentation processes on the concentration levels of minor or trace elements in tea samples is investigated. Because only free metal ions are bioavailable for the human body, it is necessary to determine their concentrations in drinking tea. The dissolution of trace elements in drinking tea is therefore studied by simulating the common Chinese style of tea percolation. Concentrations of thirteen elements including Zn, Mn, Ca, Cu, Ni, Al, K, Mg, Cd, Pb, Na, Co and Sc are determined. (author) 14 refs.; 1 fig.; 6 tabs

  15. Trace elements in Turkish tobacco determined by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Guelovali, M.C.; Guenduez, G.

    1983-01-01

    The concentration of 20 trace elements in nine brands of Turkish cigarette tobacco and in a brand of pipe tobacco ash has been determined by instrumental neutron activation analysis. The percent transference of elements into smoke has been estimated from the amounts remaining in the ash. (author)

  16. Determination of trace elements in biological material by neutron activation analysis

    International Nuclear Information System (INIS)

    Tran Van, L.; Teherani, D.K.

    1989-01-01

    Eighteen trace elements in biological materials [grass (Imperata cylindrica), mimosa plant (Mimosa pudica), rice] by neutron activation method were determined. In the comparative analysis the content of the same element was different in each material, although they were collected at the same place and the same sampling method was applied. (author) 4 refs.; 1 fig.; 1 tab

  17. Determination of trace elements by INAA in urban air particulate matter and transplanted lichens

    International Nuclear Information System (INIS)

    Bergamaschi, L.; Rizzio, E.; Profumo, A.; Gallorini, M.

    2005-01-01

    Lichens as biomonitors and neutron activation analysis as analytical technique have been employed to evaluate the trace element atmospheric pollution in the metropolitan area of the city of Pavia (Northern Italy). Transplanted lichens (Parmelia sulcata and Usnea gr. hirta) and air particulate matter have been monthly collected and analyzed during the winter 2001-2002. INAA and ET-AAS have been used for the determination of 28 elements in air particulate matter and 25 elements in lichens. Trace metals concentrations as well as the corresponding enrichment factors were evaluated and compared. (author)

  18. Determination of several trace elements in Chinese herbs with epithermal neutral activation analysis

    International Nuclear Information System (INIS)

    Chen, Chien-Yi; Chang Lai, Sheng-Pin

    2002-01-01

    For purpose of medication and health, Chinese herbs have been long adopted throughout oriental communities. Thus, more than ten trace elements in herbal medicines that are frequently consumed by children in central Taiwan were analyzed herein to explore the importance of various herbs. These elements are considered beneficial to human health in many folds. INAA was applied to determine the concentrations of elements as Al, Cl and Sc, while ENAA analyzed As, Cd, Mn, and Sb in this work. Among various local herbs, the elemental concentrations varied from 10 4 to 10 -3 μg/g. The experimental results suggest that the ENAA method can be applied successfully to analyze trace elements of As, Cd, Mn, and Sb in herbs. Yet, thirteen elements were verified, and a quantified index AT was introduced to help classifying the elements. The ATs in various Chinese herbs are also discussed herein and the accuracy is in excellent agreement with values reported in previously published data. (author)

  19. Determination of trace elements in chewing gum by neutron activation analysis

    International Nuclear Information System (INIS)

    Dietz, M.L.

    1990-01-01

    Six trace elements of nutritional or toxicological interest (Al, Ca, Cl, Mn, Na and Sr) were determined in three different brands of chewing gum by instrumental neutron activation analysis. For the particular brands of gum examined, none of the detected elements was found to be present at a level representing a substantial contribution to the total dietary intake of the element for an American adult. (author) 11 refs.; 3 tabs

  20. Determination of Trace Elements in Patients With Chronic Hepatitis B

    Directory of Open Access Journals (Sweden)

    Vahid Hosseini

    2011-10-01

    Full Text Available Chronic Hepatitis B virus (HBV infection is a major liver disease worldwide and its clinical manifestations are linked to immune response. The purpose of this study was to evaluate the relationship between selenium, copper, and zinc in comparison with transaminase level in chronic HBV patients. Serum samples of the HBV infected patients were obtained from Tooba medical center, Sari, Iran. Sixty patients were enrolled in this study (36 men and 24 women, mean age: 39.6 ± 12.2 years. The concentration of zinc, selenium, copper and transaminases were determined using an autoanalyzer system. Concentrations of selenium (0.273 ±0.056 μg/dl and zinc (2.1±0.037 was elevated in patients with low transaminase levels as were significantly different in comparison with patients with high transaminase level (P<0.05. Serum copper concentration was similar in two groups of patients. Elevated levels of transaminase concentrations were independently associated with low zinc and selenium concentrations in chronic HBV patients. It is concluded that serum zinc and selenium levels are associated with less hepatic damage in chronic HBV patients and might have a protective role during liver injury.

  1. Integration of Solid-phase Extraction with Electrothermal Atomic Absorption Spectrometry for Determination of Trace Elements

    OpenAIRE

    NUKATSUKA, Isoshi; OHZEKI, Kunio

    2006-01-01

    An enrichment step in a sample treatment is essential for trace analysis to improve the sensitivity and to eliminate the matrix of the sample. Solid-phase extraction (SPE) is one of the widely used enrichment technique. Electrothermal atomic absorption spectrometry (ETAAS) is a well-established determination technique for trace elements. The integration of SPE with ETAAS leads to further improvement of sensitivity, an automation of the measurement and the economy in the sample size, amounts o...

  2. Determination of trace elements in cigarette and tobacco by neutron activation analysis

    International Nuclear Information System (INIS)

    Nouchpramool, S.

    1988-01-01

    The objective of this work is to determine the concentration of 22 trace elements in cigarette and tobacco by instrumental neutron activation analysis in which multielements can be analyzed simultaneously with high sensitivity and reliability as well as easy and rapid. It is well known that, trace toxic elements with high concentration may be harmful for health of smokers. Since they might damage the respiratory system and might cause other diseases. The finding for this report can be used as the basis of further study on toxic of trace elements to the smoker. The results of this analysis show that the bromine content in all samples is significantly high, but the concentration of the other elements are varying from one to another. Bromine concentration might come from soil and/or smoked tobacco leaves with methyl bromide as fungicide

  3. Determination of trace elements in plant samples using XRF, PIXE and ICP-OES techniques

    International Nuclear Information System (INIS)

    Ahmed, Hassan Elzain Hassan

    2014-07-01

    The purpose of this study is to determine trace element concentration (Ca, Cu, Cr, K,Fe, Mn,Sr, and Za) in some sudanese wild plants namely, Ziziphus Abyssinica and Grewia Tenax. X-ray fluorescence ( X RF), particle-induced x-ray emission ( PIXE) and inductively coupled plasma-optical emission spectroscopy (ICP-OES) techniques were used for element determination. A series of plants standard references materials were used to check the reliability of the different employed techniques as well as to estimate possible factors for correcting the concentration of some elements that deviated significantly from their actual concentration. The results showed that, X RF, PIXE and ICP-OES are equally competitive methods for measuring Ca,K, Fe, Sr and Zn elements. Unlikely to ICP-OES seems to be superior techniques tend to be appropriate methods for Cu determination in plant samples however, for Mn element PIXE and ICP-OES are advisable techniques for measuring this element rather than X RF method. On the other hand, ICP-OES seems to be the superior techniques over PIXE and X RF methods for Cr and Ni determination in plant samples. The effect of geographical location on trace elements concentration in plants has been examined through determination of element in different species of Grewia Tenax than collected from different location. Most of measured elements showed similarity indicating there is no significant impact of locations on the difference of element contents. In addition, two plants with different genetic families namely, Ziziphus Spina Christi and Ziziphus Abyssinica were collected from the same location and screened for their trace element content. It was found that there were no difference between the two plants for Ca, K, Cu, Fe, and Sr element. However, significant variations were observed for Mn and Zn concentrations implying the possibility of using of those two elements for plant taxonomy purposes.(Author)

  4. Determination of trace elements in ground water by two preconcentration methods using atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Elhag, A. Y.

    2004-01-01

    This is a comparative study between two different methods of preconcentration done to separate the trace elements cadmium, nickel. chromium, manganese, copper, zinc, and lead in drinking (ground) water samples taken from different locations in Gezira State, central Sudan (the map); these methods are (coprecipitation) with aluminium hydroxide and by Ammonium Pyrrolidine Dithiocarbamate (APDC) using Methyl Isobutyl Ketone (MIBK) as an organic solvent; and subsequent analysis by Atomic Absorption Spectrometry (AAS) for both methods. The result of comparison showed the superiority of the (APDC) coprecipitation method over the aluminium hydroxide coprecipitation method in the total percentage recoveries of the studied trace elements in drinking (ground) water samples, such results confirm previous studies. This study also involves direct analysis of these water samples by atomic absorption spectrometry to determine the concentrations of trace elements Cadmium, Nickel, Chromium, Manganese, Copper, Zinc and Lead and compare it to the corresponding guide line values described by the World Health Organization and the maximum concentrations of trace elements in drinking water permitted by the Sudanese Standards and Metrology Organizations (SSMO), where the concentrations of some elements in some samples were found to be different than the described values by both of the organizations. The study includes a trial to throw light on the effect of the proximity of the water samples sources to the Blue Nile river on its trace elements concentrations; no relation was proved to exist in that respect.(Author)

  5. Determination of artificial and natural radionuclides and others trace elements in environmental samples form Antarctica

    International Nuclear Information System (INIS)

    Schuch, L.A.; Godoy, J.M.; Nordemann, D.J.R.

    1994-01-01

    The results of the radioactive elements concentrations, determined by gamma spectrometry and the others trace elements determined by neutron activation analysis of several environmental samples (soils, marine sediments, algae mosses and lichens) in Comandante Ferraz Antartica Station are presented. The high concentrations of Cs-137 were found in lichens and mosses samples and the soils and sediments showed concentrations of natural radionuclides. (C.G.C.). 8 refs, 1 fig, 3 tabs

  6. Determination of some trace elements in biological samples using XRF and TXRF techniques

    International Nuclear Information System (INIS)

    Khuder, A.; Karjou, J.; Sawan, M. K.

    2006-07-01

    XRF and TXRF techniques were successfully used for the multi-element determination of trace elements in whole blood and human head hair samples. This was achieved by the direct analysis using XRF technique with different collimation units and by the optimized chemical procedures for TXRF analysis. Light element of S and P were preferably determined by XRF with primary x-ray excitation, while, elements of K, Ca, Fe, and Br were determined with a very good accuracy and precision using XRF with Cu- and Mo-secondary targets. The chemical procedure dependent on the preconcentration of trace elements by APDC was superiorly used for the determination of traces of Ni and Pb in the range of 1.0-1.7 μg/dl and 11-23 μg/dl, respectively, in whole blood samples by TXRF technique; determination of other elements as Cu and Zn was also achievable using this approach. Rb in whole blood samples was determined directly after the digestion of samples using PTFE-bomb for TXRF analysis. (author)

  7. Determination of trace elements in bottled water in Greece by instrumental and radiochemical neutron activation analyses

    International Nuclear Information System (INIS)

    Soupioni, M.J.; Symeopoulos, B.D.; Papaefthymiou, H.V.

    2006-01-01

    Four different bottled water brands sold in Greece in the winter of 2001-2002 were analyzed for a wide range of chemical elements, using neutron activation analysis (NAA). The elements Na and Br were determined instrumentally (INAA), whereas the other metals and trace elements radiochemically (RNAA). The results indicated that the mean level of all the elements determined in the samples were well within the European Union (EU) directive on drinking water and accomplish the drinking water standards of the World Health Organisation (WHO) as well as of the Food and Drug Administration (FDA). (author)

  8. Report on the intercomparison for the determination of trace elements in Lake Sediment (SL-1)

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1979-02-01

    The determination of trace element concentrations including those of the rare-earths in geological samples has gained much importance during the past decade. Knowledge of the concentrations of specific elements and of their ratios have proved essential for the understanding of the development of geological strata. With increasing use of instruments in analysis, reference samples have become essential for their calibration and various international organizations have issued reference materials to monitor precision and accuracy in chemical determinations. The IAEA has in the past organized several intercomparisons and prepared reference samples of geochemical materials. The present report deals with a recent intercomparison on the determination of trace elements in Lake Sediment (Sl-1) carried out in 1977-1978 and involving the participation of 43 institutes who returned a total of 2535 individual results on 43 elements.

  9. The Determination Of Trace Element Levels In Diet By Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Kukuh, Ratnawati; Djojosubroto, Harjoto

    2002-01-01

    Trace element levels in foodstuff are normally low. Although the levels are low, certain trace elements which are called essential trace elements have an important role in metabolism process. Deficiency or intoxication of essential trace elements may lead to abnormal health. In this study the levels of Zn, Fe, AI, Mn, and Co in diet samples were determined by neutron activation analysis, and then the daily intakes of these elements were estimated. The samples were prepared by duplicate diet method, representing those that were consumed by population from West, Central and East Java. Following the collection the respective samples were blended, then were freeze dried at-54 o c. The elemental quantification were performed by neutron activation analysis. The traceability of the determination was ensured using standard reference material NIST-SRM-1548a. The results show that the daily intake for Zn were 2.8-22.8 mg/day (reference value were 5- 40 mg/day), Fe were 3.1-26.5 mg/day (reference value were 6-40 mg/day), AI were 4,2-32.9 mg/day (reference value were 2-45 mg/day), Mn were 1.0-5,6 mg/day (reference value were 0.4-10,0 mg/day), and Co were 0,005-0,074 mg/day (reference value were 0.005 -1.8 mg/day

  10. Determination of trace elements concentrations in Grewia tenax plants collected from Darfur Region-Sudan

    International Nuclear Information System (INIS)

    Alzain, H. A; Ebrahim, A. M; Salih, A. M; Ali Altom, M. S.

    2016-01-01

    This study is aimed to determine trace elements concentrations (Ca, Cu, Cr, K,Fe, Mn, Ni, Sr and Zn) in Grewia tenax collected from Darfur state western of Sudan. X- ray fluorescence (X RF) technique was used to determine elements concentration. A series of plant standard reference materials(ISE 2012-1) were used to check the reliability of employed technique by comparing the obtained results with the certified values, to estimate possible factors for correcting the concentration of some elements. The results showed that, X RF is a suitable method for measuring Ca, Cu, K, Fe, Mn, Sr and Zn elements. On the other hand, X RF for Cr and Ni determination in plant samples, these elements have showed a deviation from their certified values. Concentration of Fe was about 35 mg/kg in Grewia tenax samples where as K and Ca showed maximum levels about 16000 and 8500 mg/kg respectively, Cu showed minimum concentration about 10 mg/kg. The effect of geographical location on trace elements concentration in plants has been examined through determination of element in different species of Grewia tenax that collected from different locations in Darfur region. Most of the measured elements showed that there is no significant impact of locations on the difference of element contents.(Author)

  11. Determination of trace elements in coffee beans and instant coffee of various origins by INAA

    International Nuclear Information System (INIS)

    Zaidi, J.H.; Fatima, I.; Arif, M.; Qureshi, I.H.

    2006-01-01

    Extensive use of coffee, by one-third of world's population, entails the evaluation of trace element contents in it. Instrumental neutron activation analysis (INAA) was successfully employed to determine the concentration of 20 trace elements (essential, toxic and nonessential) in four samples of coffee beans of various origins and two instant coffee brands most commonly consumed in Pakistan. Base-line values of certain toxic and essential elements in coffee are provided. The daily intake of essential and toxic elements through coffee was estimated and compared with the recommended values. The cumulative intake of Mn is four times higher than the recommended value and that of toxic elements is well below the tolerance limits. (author)

  12. Method to determine trace elements in water samples by neutron activation analysis

    International Nuclear Information System (INIS)

    Kueppers, G.; Erdtmann, G.

    1981-05-01

    For the determination of trace elements in water by neutron activation analysis irradiation porcedures and chemical separation procedures have been developed. Irradiation in melted quarz glass ampoules in the presence of a platinum wire (for recombination of the oxyhydrogen gas produced by radiolysis) proved successfull with different variants of the irradiation methods, as long irradiation periods without pressure build-up could be achieved. Possible falsifications of the analysis results were investigated in detail (losses by absorption on vessel walls etc.). The irradiated samples can be measured directly with a gamma ray spectrometer and from the radionuclides found the trace element contents may be calculated. More sensitive determinations are possible if the radionuclides are chemically separated. Procedures for removing the matrix activities, for the separation of the radionuclides in groups of elements and for the isolation of single elements have been developed. For especially sensitive determination of some elements selective separation procedures for antimony, cadmium, selenium, mercury and uranium have been developed. The analytical procedures described have been applied to trace element determinations in river water, glacier ice and water solutions from technical processes. (orig./RB) [de

  13. Application of neutron activation analysis to trace elements determinations in lung samples

    International Nuclear Information System (INIS)

    Rogero, S.O.

    1991-01-01

    The purpose of this work was to apply the instrumental neutron activation analysis method to determine trace elements in lung samples from smokers and non smokers. Samples of lung tissues and lymph nodes from pulmonary hilum analyzed were collected from autopsies by researchers from Faculdade de Medicina da USP. (author)

  14. Determination of trace elements (Fe, Cu and Zn) in serum and tail ...

    African Journals Online (AJOL)

    Strong and poor relationships between the levels of trace elements in blood, tissue and hair have been determined in various studies. The horses in this study have been fed with dry straw and artificial feed in winter months, with fresh grass in autumn and spring. The purpose was to investigate possible changes in the ...

  15. Determination of trace elements in BCR single cell protein via destructive neutron activation analyses

    International Nuclear Information System (INIS)

    Tjioe, P.S.; Goeij, J.J.M. de; Nooijen, J.L.; Kroon, J.J.

    1978-10-01

    The amount of some trace elements in single cell protein (SCP), a product of BP Research Centre at Sunbury-at-Thames, England, was determined by neutron activation analysis. The SCP-samples were irradiated in the reactor of the Interuniversity Reactor Institute at Delft in a neutron flux of 1.0x10 13 n/cm 2 s for 12 hours. Samples of Bowen's Kale were used as reference material. After a decay of two or three days the samples were chemically destroyed, and the trace elements were separated. The quantity of the following elements was determined by measuring the γ-activity by means of a scintillation counter: antimony, cadmium, mercury, arsenic and selenium. The amounts of these elements in the SCP and in the reference material were tabled

  16. Report on intercomparison V-8 of the determination of trace elements in rye flour

    International Nuclear Information System (INIS)

    Pszonicki, L.; Veglia, A.; Dybczynski, R.; Suschny, O.

    1982-01-01

    The participants were requested to determine as many elements as they could from among the following 29: As, Be, Ca, Cd, Cl, Co, Cr, Cu, F, Fe, Ga, Hg, I, K, Mg, Mn, Mo, Na, Ni, P, Pb, Sb, Se, Si, Sn, Tl, U, V and Zn. While six of these elements (Be, Ga, Sn, Tl, U, V) were not determined by any laboratory, some participants on the other hand determined several elements which had not been ordered for such as As, Al, Au, Ba, Br, Cs, Eu, La, N, Rb, S, Sc, Sr, Ti and Y. In total, 34 laboratories submitted results of 1,207 individual determinations (301 laboratory means) on 38 elements. The methods most often employed in this intercomparison were neutron activation analysis (47% of all results) and atomic absorption (20%). The results of the intercomparison demonstrated again the difficulties in the determination of trace elements in organic materials. The agreement between participating laboratories was in general poor

  17. Determination of trace element impurities in aspirin tablets by neutron activation analysis

    International Nuclear Information System (INIS)

    Iskander, F.Y.; Klein, D.E.; Bauer, T.L.

    1986-01-01

    Twenty-five trace and minor elements in five different Egyptian aspirin brands (Aspo, Askin, Aspocid, Aspeol and Rivo) were determined by instrumental neutron activation analysis. It was concluded that the concentration of As, Ba, Br, Co, Cr, Fe (except in Aspocid), Mg, Mn, Rb, Se, Sr and Zn in the Egyptian brands is below or within the concentration range reported for these elements in 16 American aspirin and aspirin-like brands. (author)

  18. Trace Elements in Human Myocardial Infarction Determined by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Wester, P.O.

    1965-05-01

    By means of neutron activation analysis, injured and adjacent uninjured human heart tissue from 12 autopsy cases with myocardial infarction are investigated with respect to the concentration of 23 trace elements. The bulk elements K, Na and P are also determined. A recently developed ion-exchange technique, combined with subsequent y-spectrometry, is used. The following trace elements are determined: Ag, As, Au, Ba, Br, Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Hg, La, Mo, Rb, Sb, Sc, Se, Sm, Zn and W. In the injured tissue compared to the uninjured, calculation on a wet weight basis showed a decrease in Co, Cs, K, Mo, P, Rb and Zn, and an increase in Br, Ca, Ce, La, Na, Sb and Sm. The differences in Ca, La, Mo, P and Zn are dependent on the age of the myocardial infarction, and the regression lines for these elements are given. The concentration of the trace elements in uninjured tissue from infarcted hearts is compared to the concentration of these elements in normal heart tissue, determined in a previous study. In the uninjured tissue from infarcted hearts a decrease is found in Cu and Mo, and an increase in As and Ce

  19. Trace Elements in Human Myocardial Infarction Determined by Neutron Activation Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Wester, P O

    1965-05-15

    By means of neutron activation analysis, injured and adjacent uninjured human heart tissue from 12 autopsy cases with myocardial infarction are investigated with respect to the concentration of 23 trace elements. The bulk elements K, Na and P are also determined. A recently developed ion-exchange technique, combined with subsequent y-spectrometry, is used. The following trace elements are determined: Ag, As, Au, Ba, Br, Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Hg, La, Mo, Rb, Sb, Sc, Se, Sm, Zn and W. In the injured tissue compared to the uninjured, calculation on a wet weight basis showed a decrease in Co, Cs, K, Mo, P, Rb and Zn, and an increase in Br, Ca, Ce, La, Na, Sb and Sm. The differences in Ca, La, Mo, P and Zn are dependent on the age of the myocardial infarction, and the regression lines for these elements are given. The concentration of the trace elements in uninjured tissue from infarcted hearts is compared to the concentration of these elements in normal heart tissue, determined in a previous study. In the uninjured tissue from infarcted hearts a decrease is found in Cu and Mo, and an increase in As and Ce.

  20. [Determination of polysaccharide from Chinese medicine Morinda officinalis how and its trace elements analysis].

    Science.gov (United States)

    Wu, Yong-Jun; Liu, Jie; Wu, Yu-Ming; Liu, Li-E; Zhang, Hong-Quan

    2005-12-01

    Polysaccharide was extracted from morinda officinalis how by back-flowing with 80% ethanol for 1 h, and the method of improved phenol-sulfuric acid spectroscopy was adopted to determine the content of morinda officinalis how polysaccharide. As for its trace elements, the atomic absorption spectroscopy was used to detect the content of Zn, Fe and Cu, which were compared with its fake; and cold atomic fluorometry was applied to determine the trace mercury. The results were satisfactory, which can give reference about the effective components of morinda officinalis how, and will help to exploit it.

  1. Trace element determination in tomato puree using particle induced X-ray emission and Rutherford backscattering

    International Nuclear Information System (INIS)

    Romero-Davila, E.; Miranda, J.

    2004-01-01

    Particle induced X-ray emission (PIXE) and Rutherford backscattering spectrometry (RBS) were used to determine the concentrations of trace elements in samples of 12 tomato puree brands sold in the Mexican market. While RBS offered information about the main elements present in the matrix, PIXE gave results on trace elements. As a whole, data for 17 elements (C, N, O, Na, Mg, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, and Zn) were obtained. To evaluate the results, a comparison with brands from USA, Japan, Colombia, and Chile was carried out, using tomato purees produced following the domestic technology recipe. Additionally, the results were considered in the light of the Codex Alimentarius and the Mexican standard. It was found that all of the brands fall within the limits established by these standards, being of the same order of magnitude as the foreign brands. (author)

  2. Trace elements in Turkish tobacco determined by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Gulovali, M.C.

    1977-01-01

    This study was undertaken to determine the concentration of trace elements in nine different brands of Turkish cigarette tobacco, pipe tobacco and tobacco ash. Instrumental neutron activation analysis was employed, and a gamma-ray spectrometer consisting of 40 cm 3 Ge(Li) detector coupled to 1024 and 4096-channel analyzers were used. Samples were irradiated at a thermal neutron flux of about 10 13 cm -2 sec -1 . Concentrations of Na, K, Sc, Cr, Fe, Co, Zn, As, Se, Br, Rb, Sb, Cs, Ba, La, Ce, Eu, Hf, Hg and Th were determined in tobacco and ash; percent transference of these elements into ash were calculated. It was found out that trace elements in cigarette tobacco are left in the ash but only a small percentage is transferred into the smoke

  3. Informative importance of determination of trace elements in biologocal mediums in patients with endocrine pathology

    Directory of Open Access Journals (Sweden)

    Ирина Николаевна Андрусишина

    2015-07-01

    Full Text Available Aim. The changes of mineral metabolism in human organism caused by the deficiency or excess of trace elements in environment (air, food stuffs, water can lead to disorder of functional status of organism.An excess or deficiency of the certain metals disturb the balance of metabolic processes in organism that causes the different changes in endocrine system too. That is why the aim of research was to detect the peculiarities of distribution of macro and trace elements in patients with different endocrine pathology and to show the reasonability of the complex approach in assessment of microelementoses at hyperthyroidism and diabetes mellitus.Methods. The balance of 15 macro and trace elements in different biological mediums (hairs, whole blood, blood serum, urine was studied using EAAS and AES-ICP methods.Result. There was demonstrated the high informative importance of determination of K, Mg, Mn, Cr, Zn at pancreas pathology and Cr, Mn, Se, Zn- at thyroid pathology in human. There was detected that endocrine pathology is characterized with the surplus accumulation of Al, As and Pb in organism of examined patients.Conclusions. To increase the reliability and efficiency of the clinical diagnostics of endocrine human pathology there was demonstrated the high informative importance of the complex approach in choice of biological mediums at assessment of the trace elements imbalance. 

  4. XRF determination of trace and major elements using a single-fused disc

    International Nuclear Information System (INIS)

    Thomas, I.R.; Haukka, M.T.

    1978-01-01

    A new fusion method using lithium metaborate, suitable for the determination of major and trace elements by X-ray fluorescence analysis (XRF), has proven to be of comparable accuracy to other XRF methods for the ten major rock-forming oxides. The very low dilution allows determination of trace elements with a decrease in sensitivity of about a factor of 2 compared with XRF determination using pressed-powder pellets. A feature of the method is the flexibility of sample preparation allowed: the matrix-correction parameters may be used for a wide range of dilutions (sample/flux ratios), no 'Loss' correction is necessary, and imperfect or inhomogeneous discs may be crushed and pressed pellets made of the glass powder when required. Considerable savings in the time during preparation, analysis and correction of results are possible with current automation because of streamlining procedures

  5. Levels of trace elements in different varieties of wheat determined by Atomic Absorption Spectroscopy

    International Nuclear Information System (INIS)

    Mohamed, A.E.; Taha, G.M.

    2003-01-01

    Trace elements Ag, Au, Ca, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, Sr and Zn were determined in six wheat samples purchased from the open market in different localities (Egypt, Saudi Arabia, Yemen, Oman, Dubai and Australia). The dried powdered samples were decomposed in HNO3-HClO4 acids mixtures and elements were determined using recording atomic absorption spectrophotometer. The results were within the safety baseline of all the assayed elements. Certified biological standards, Brown's Kale (BK), Orchard Leaves (OL) and tomato leaves (TOML) were used to assure the accuracy of results. However, Co, Pb and Sr were absent from samples except the Egyptian samples. The obtained databases were statistically treated. Several significant and strong positive correlation coefficients (r=0.506-1.00) between the groups of elements were observed. On the other hand, strong negative correlations (r=0.492-0.873) between another group of elements were also shown. (author)

  6. Trace element composition and distribution in micron area of dinosaur eggshell fossils determined by proton microprobe

    International Nuclear Information System (INIS)

    Chen Youhong; Zhu Jieqing; Wang Xiaohong; Wang Yimin

    1997-01-01

    The scanning proton microprobe and micro-PIXE quantitative analysis technique have been used to determine composition and distribution of the trace elements in micron areas of dinosaur eggshell fossils from the stratum of Upper Cretaceous system at Nanxiong Basin in Guangdong Province, China. The study shows that the trace elements mainly include Ti, V, Cr, Mn, Co, Ni, Cu, Zn, As, Rb, Sr, Y, Zr, Sb, Ba and Pb in the micron area, but they present different distributions. While the element Sr is mainly enriched in the near surface layer, others mainly reside in the near inner layer. A preliminary discussion on the reason of the dinosaur extinction is given based on the above study

  7. Trace element composition and distribution in micron area of dinosaur eggshell fossils determined by proton microprobe

    International Nuclear Information System (INIS)

    Chen Youhong; Zhu Jieqing; Wang Xiaohong; Wang Yimin

    1997-01-01

    The scanning proton microprobe and micro-PIXE quantitative analysis technique have been used to determine composition and distribution of the trace elements in micron areas of dinosaur eggshell fossils from the stratum of Upper Cretaceous system at Nanxiong Basin in Guangdong Province, China. The study shows that the trace elements mainly include Ti, V, Cr, Mn, Co, Ni, Cu, Zn, As, Rb, Sr, Y, Zr, Sb, Ba and Pb in the micron area, but they present different distributions. While the elements Sr is mainly enriched in the near surface layer, others mainly reside in the near inner layer. A preliminary discussion on the reason of the dinosaur extinction is given based on the above study

  8. Trace element determinations in brain tissues from normal and clinically demented individuals

    International Nuclear Information System (INIS)

    Saiki, Mitiko; Genezini, Frederico A.; Leite, Renata E.P.; Grinberg, Lea T.; Ferretti, Renata E.L.; Suemoto, Claudia; Pasqualucci, Carlos A.; Jacob-Filho, Wilson

    2013-01-01

    Studies on trace element levels in human brains under normal and pathological conditions have indicated a possible correlation between some trace element concentrations and neurodegenerative diseases. In this study, analysis of brain tissues was carried out to investigate if there are any differences in elemental concentrations between brain tissues from a normal population above 50 years of age presenting Clinical Dementia Rating (CDR) equal to zero (CDR=0) and that cognitively affected population ( CDR=3). The tissues were dissected, ground, freeze-dried and then analyzed by instrumental neutron activation analysis. Samples and elemental standards were irradiated in a neutron flux at the IEA-R1 nuclear research reactor for Br, Fe, K, Na, Rb, Se and Zn determinations. The induced gamma ray activities were measured using a hyperpure Ge detector coupled to a gamma ray spectrometer. The one-way ANOVA test (p< 0.05) was used to compare the results. All the elements determined in the hippocampus brain region presented differences between the groups presenting CDR=0 and CDR=3. In the case of frontal region only the elements Na, Rb and Zn showed differences between these two groups. These findings proved the correlation between elemental levels present in brain tissues neurodegenerative diseases. Biological standard reference materials SRM 1566b Oyster Tissue and SRM 1577b Bovine Liver analyzed for quality control indicated good accuracy and precision of the results. (author)

  9. Multi-elemental determination of trace elements in deep seawater by inductively coupled plasma mass spectrometry with resin preconcentration

    International Nuclear Information System (INIS)

    Sumida, Takashi; Nakazato, Tetsuya; Tao, Hiroaki

    2003-01-01

    A miniaturized column (ca. 3 mm i.d., 40 mm length), packed with a chelating resin (0.2 g) with iminodiacetic acid groups (Muromac A-1), was tested for the preconcentration of trace elements in seawater. After preconcentration, the column was washed with ammonium acetate buffer (pH 5.5) and water to remove the major elements, such as Ca and Mg, and was then eluted with 4 ml of 2 mol l -1 nitric acid. Twenty-six trace elements were determined by inductively coupled plasma mass spectrometry and inductively coupled plasma emission spectrometry. The necessary volume of the seawater sample was only 200 ml. The recoveries for most of the elements tested were over 90%, although those for Al, V and Th were around 70%. The trueness and precision were evaluated by analyzing a standard reference material of seawater (NASS-4, NRC Canada). The observed values obtained with the present method showed good agreement with the certified values. The present method was also applied to deep seawater samples collected at Muroto, Japan. A difference in the rare earth element pattern, especially the Ce anomaly, between the deep seawater sample and the surface seawater sample was observed, as well as the differences of the concentrations of many trace elements. (author)

  10. Determination of trace elements in seawater using Mg-scavenger as preconcentration agent, and neutron activation analysis

    International Nuclear Information System (INIS)

    Andersen, B.

    1986-01-01

    In order to determine trace elements in seawater, a preconsentration method based on coprecipitation on Mg(OH) 2 is presented. Different parameters influencing the carrying effects have been investigated using model solutions and radioactive tracers. The deposit and solution are separated by filtration. Filter with deposit is stored in quarts ampules for later determination of trace elements by means of neutron activation analysis

  11. Determination of trace elements by neutron activation analysis using dinonylnaphtalene sulfonic acid as a preconcentrating agent

    International Nuclear Information System (INIS)

    Yang, M.H.; Chen, P.Y.; Tseng, C.L.; Yeh, S.J.; Weng, P.S.

    1977-01-01

    Dinonylnaphthalene sulfonic acid (HD) has been used as a preconcentrating agent to enrich trace metal ions and to separate the interfering elements such as Na, K, Cl and Br, which normally exist in the natural aqueous systems. Experiments were performed by extracting the ions in the aqueous medium with HD in n-hexane and subsequently backextracted into a minimal volume of acid solution. Factors influencing the extraction efficiency of the ions of interest were investigated. The preconcentration technique has been successfully applied to the determination by neutron activation analysis of trace elements in natural water and biological materials. Both short-lived nuclides (Mg, Al, Ca, Mn) and long-lived nuclides (Sm, Eu, Zn, La, Cr, Sc, Fe, Co) in the ppb-level concentrations were determined. (T.G.)

  12. Determination of 11 trace elements in U3O8 CRMs by ICP-AES

    International Nuclear Information System (INIS)

    Liu Husheng

    1994-01-01

    The TBP extractant-containing resin and extraction chromatography technique were used to separate 11 trace elements in U 3 O 8 CRMs. The sample was separated at a flow rate of 0.5 mL/min with 3 mol/L HNO 3 as medium. A model 975 ICP direct reading spectrometer was used to determine the trace elements of Ca, Cd, Cr, Cu, Fe, Mg, Mn, Mo, Ni, Pb and Sn in U 3 O 8 CRMs. The lowest quantitatively determinable concentration of impurities in U 3 O 8 CRMs are 0.02-1.6 μg/g. The RSD is less than 10%. The proposed method provides excellent and accurate analytical data for the U 3 O 8 samples prepared as certified reference materials (CRMs)

  13. Determination of trace elements in ceramic uranium dioxide pellets powders CRMs by ICP-AES

    International Nuclear Information System (INIS)

    Liu Husheng; Li Jun

    1997-01-01

    The 237-quaternary ammonium extraction resin chromatography is used to the separation of 6 trace elements in ceramic uranium dioxide pellets powders, which are used as certified reference materials (CRMs). The sample is dissolved in 6.5 mol/L HNO 3 and uranium is separated by chromatographic column. the 6 trace elements Al, Ba, Co, Ta, Ti and V contained in the elutriant are determined by using ICP directly reading spectrometer. For a 300 mg sample, the lowest determinable concentration of impurities in ceramic UO 2 pellets powders CRMs is (0.016-0.250) x 10 -6 . The relative standard deviation is less than 7.5%. The proposed method provides excellent and accurate analytical data for the ceramic UO 2 pellets powders samples (CRMs)

  14. The determination of some trace elements in sulphide concentrates by spectrophotometry

    International Nuclear Information System (INIS)

    Shelton, B.J.; Komarkova, E.; Josephson, M.; Cook, E.B.T.; Dixon, K.

    1977-01-01

    The report describes the determination of trace amounts (as low as 1 to 10 p.p.m. depending on the element) of arsenic, germanium, molybdenum, nickel, phosphorus, selenium, tellurium, tin, and titanium in sulphide concentrates. The proposed methods, which are detailed in the appendices, are adaptations of established procedures that were modified to allow for the complex nature of the concentrates to be analysed

  15. Determination of five trace elements in leaves in Nanfang sweet orange by flame atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Li Fangqing

    2006-01-01

    The five trace elements of copper, zinc, manganese, iron and cobalt in leaves of Nanfang sweet orange are determined by flame atomic absorption spectrometry. The technique is simple, precise and sensitive. The effect of the type of digesting solution (mixed acid), the ratio of mixed acid, the volume of digesting solution and the time of digesting are investigated in details. The results show that leaves of Nanfang sweet orange contain higher amount of iron and zinc. (authors)

  16. X-ray fluorescence analysis for trace element determination in foodstuff chemistry

    International Nuclear Information System (INIS)

    Wildanger, W.

    The physical fundamentals of X-ray fluorescence analysis are given and the routine spectrometers described. The basic principles are given of analytical methods used in qualitative and quantitative fluorescence analyses. Examples are given of the use of the method in a number of fields and the possibility and usefulness is discussed for the determination of trace elements in foodstuffs. The preparation of samples, preliminary concentration of components and calibration methods are discussed. (M.K.)

  17. Trace elements in the diets of Turkish children determined by INAA

    International Nuclear Information System (INIS)

    Aras, N.K.; Mauerhofer, E.; Naidu, R.K.; Arcasoy, A.; Denschlag, H.O.

    1992-01-01

    The role of toxic and essential trace elements in human diet is increasingly important because of environmental problems and the increasingly sophisticated industrial treatment of food products. Instrumental neutron activation analysis (INAA) is particularly well suited for multielement determinations. In order to test and demonstrated the usefulness of the method in connection with the fast pneumatic tube system of the Mainz TRIGA reactor, the authors have analyzed six diet samples of Turkish children

  18. Neutron activation analysis for environmental trace element research determination of elemental composition of sediments in the Sea of Galillee, Israel

    Energy Technology Data Exchange (ETDEWEB)

    Lavi, N; Ne` eman, E; Brenner, S; Butenko, V [Tel Aviv Univ. (Israel). Medical School

    1996-12-01

    The aims of this work were to: a) demonstrate the effectiveness of instrumental neutron activation analysis for determining the background concentrations of trace elements in the sediments collected from the Sea of Gallile. b) determine the advantage factors for epithermal neutron irradiation. c) determine the contribution of silicon to the total {sup 28}Al activity by the {sup 28}Si(n,p){sup 28}Al reaction. c) check the validity of the method by determining the elemental content of U.S. NBS Standard Reference Material SRM-1633a (fly ash). d) calculate the average enrichment factors for the elements in sediments . e) determine the concentrations of the artificial radionuclides {sup 134}Cs, {sup 137}Cs and the naturally occurring radionuclides {sup 40}K, {sup 226}Ra and {sup 232}Th (authors).

  19. The determination of trace elements in uranium ores by x-ray fluorescence spectrometry

    International Nuclear Information System (INIS)

    De Villiers, W. van Z.

    1983-11-01

    The determination of 17 trace elements (As, Ba, Co, Cr, Cu, Mo, Nb, Ni, Pb, Rb, Sr, Th, U, V, Y, Zn and Zr) in uranium ores by x-ray fluorescence spectrometry was investigated in this study. The determination of major elements was also necessary for the calculation of mass absorption coefficients. Initially a method was developed for the determination of the elements of interest in unmineralised silicates. Correction for absorption of radiation by the sample were made by means of mass absorption coefficients which were obtained from the relation between the inverse of the mass absorption coefficient and the intensity of the Compton scattering peak. The Feather and Willis method was used for determining the background intensity at the peak positions as well as for mass absorption coefficients. It was observed that the background intensity in the region of the uranium lines increases with increasing uranium content of the sample

  20. Determination of several trace elements in Chinese herbs with epithermal neutral activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Chien-Yi [Chung Shan Medical Univ., Inst. of Biochemistry, Taiwan (China); Chang Lai, Sheng-Pin [Chung Shan Medical Univ. Hospital, Dept. of Nuclear Medicine Chief, Taiwan (China)

    2002-04-01

    For purpose of medication and health, Chinese herbs have been long adopted throughout oriental communities. Thus, more than ten trace elements in herbal medicines that are frequently consumed by children in central Taiwan were analyzed herein to explore the importance of various herbs. These elements are considered beneficial to human health in many folds. INAA was applied to determine the concentrations of elements as Al, Cl and Sc, while ENAA analyzed As, Cd, Mn, and Sb in this work. Among various local herbs, the elemental concentrations varied from 10{sup 4} to 10{sup -3} {mu}g/g. The experimental results suggest that the ENAA method can be applied successfully to analyze trace elements of As, Cd, Mn, and Sb in herbs. Yet, thirteen elements were verified, and a quantified index AT was introduced to help classifying the elements. The ATs in various Chinese herbs are also discussed herein and the accuracy is in excellent agreement with values reported in previously published data. (author)

  1. Determination of trace elements in wool fibre by instrumental neutron activation analysis and relation between trace element contents and quality of wool

    International Nuclear Information System (INIS)

    Eozyol, H.

    1990-01-01

    Wool samples were analyzed by neutron activation analysis and 17 elements, Al, Ag, Au, As, Br, Ca, Co, Cr, Cu, Fe, La, Mg, Mn, Na, Sb, Se and Zn were measured quantitatively. The presence of seven others, Ce, Eu, I, Mo, Te and W was noted. Since several elements, such as Cd, Hg and Pb could not be conveniently determined by NAA, Atomic Absorption Spectroscopy (AAS) was used instead. Cu and Zn were also analyzed by NAA and AAS to compare these two methods. Mechanical properties of samples were measured and the relations between the trace element contents and properties were investigated. (author) 16 refs.; 7 tabs

  2. Particle induced X-ray emission and complementary nuclear methods for trace element determination; Plenary lecture

    Energy Technology Data Exchange (ETDEWEB)

    Johansson, S A.E. [Lund Univ. (Sweden). Dept. of Nuclear Physics

    1992-03-01

    In this review the state-of-the-art of particle induced X-ray emission (PIXE) methods for the determination of trace elements is described. The developmental work has mostly been carried out in nuclear physics laboratories, where accelerators are available, but now the increased interest has led to the establishment of other dedicated PIXE facilities. The reason for this interest is the versatility, high sensitivity and multi-element capability of PIXE analysis. A further very important advantage is that PIXE can be combined with the microbeam technique, which makes elemental mapping with a spatial resolution of about 1 {mu}m possible. As a technique, PIXE can also be combined with other nuclear reactions such as elastic scattering and particle-induced gamma emission, so that light elements can be determined. The usefulness of PIXE is illustrated by a number of typical applications in biology, medicine, geology, air pollution research, archaeology and the arts. (author).

  3. use of x-ray fluorescence spectrometry to determine trace elements ...

    African Journals Online (AJOL)

    NIJOTECH

    Abstract. This paper deals with application of X-ray fluorescence spectrometry for the detection of trace elements in graphic. An X-ray spectrometer was constructed and used to carry out measurements on graphite spheres impregnated with different chemical elements. The intensities of the lines of these trace elements, ...

  4. Trace element determination in soft tissues of marine bivalves by activation analysis

    International Nuclear Information System (INIS)

    Fukushima, M.; Tamate, H.; Nakano, Y.

    2003-01-01

    Trace elements in soft tissues of marine bivalves were determined by neutron activation analysis (NAA) and photon activation analysis (PAA). Elemental levels of Ag, As, Br, Co, Cu, Fe, I, Mn, Ni, Rb, Se, and Zn in the organs of giant ezoscallos, rock oysters, and giant crams were obtained. The metal-bound proteins were extracted from the mantles and hepatopancreases of rock oysters. By irradiating the fraction obtained by HPLC gel chromatography, the possibility for the existence of an Ag bound protein in the mantles was found. (author)

  5. Determination of trace elements in human brain tissues using neutron activation analysis

    International Nuclear Information System (INIS)

    Leite, R.E.P.; Jacob-Filho, W.; Grinberg, L.T.; Ferretti, R.E.L.

    2008-01-01

    Neutron activation analysis was applied to assess trace element concentrations in brain tissues from normal (n = 21) and demented individuals (n = 21) of both genders aged more than 50 years. Concentrations of the elements Br, Fe, K, Na, Rb, Se and Zn were determined. Comparisons were made between the results obtained for the hippocampus and frontal cortex tissues, as well as, those obtained in brains of normal and demented individuals. Certified reference materials, NIST 1566b Oyster Tissue and NIST 1577b Bovine Liver were analyzed for quality of the analytical results. (author)

  6. Determination of short-lived trace elements in environmental samples by neutron activation analysis

    International Nuclear Information System (INIS)

    Wardani, S.; Sihombing, E.; Hamzah, A.; Rochidi; Hery, P.S.; Hartaman, S.; Iman, J.

    1998-01-01

    Concentration of a short-lived trace elements in environmental samples were determined by neutron activation analysis, a counting loss often occur due to the high counting rate. A Pile-Up Rejecter (PUR) electric circuit was installed in counting a short-lived trace elements by a γ-ray spectrometer in order to correct a counting loss. The samples were irradiated for 30∼60 seconds at neutron flux of 3.5 x 10 12 n.cm -2 .s -1 , then the samples cooled for 120 second and counted for 180 second using this system. The nuclides concentration in the varieties environmental samples have a difference analysis result, was more accurate and precise, which the measured result would be 30 % more higher by PUR system than the result would be counted using a conventional γ-ray spectrometry method

  7. Determination of trace and toxic elements in marine sediments collected from the strait of Malacca, Malaysia

    International Nuclear Information System (INIS)

    Wee Boon Siong; Abdul Khalik Hj. Wood

    2007-01-01

    The Strait of Malacca has been a major route for international trade with heavy traffic of large vessels navigating through the narrow waterway everyday. Beside, the Strait of Malacca has some natural ecosystem which requires proper protection from human activities. Therefore, the Malaysian government has initiated a project to monitor the pollution level at the Strait of Malacca. As a result, sampling expeditions had been conducted to collect marine samples to be analyzed for trace and toxic elements as well as organic pollutions and radionuclides. The focus of this report is to determine trace and toxic element concentration in surface sediment samples collected from 18 sampling locations at the Strait of Malacca was reported. (author)

  8. Determination of trace elements in total particulate matter of cigarette smoke by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Mishra, U.C.; Shaikh, G.N.

    1985-01-01

    Cigarette smoke contains many trace elements hazardous for human body. Tobacco samples were analyzed for their trace element contents and the results were reported earlier. This paper presents results on the trace element content analyzed in cigarette smoke using an automatic smoking machine developed in laboratory to simulate actual smoking pattern. The trace element levels in the total particulate matter samples of the cigarette smoke collected on filter papers were measured and compared with those of cigarette smoke condensate reported in the literature. Both methods of collection give comparable results. (author)

  9. Determination of trace elements: Neutron-activation analysis in geochemistry and cosmochemistry

    International Nuclear Information System (INIS)

    Kolesov, G.M.

    1994-01-01

    Geochemistry, like cosmochemistry, open-quotes studies chemical elements hor-ellipsis of the crust and hor-ellipsis the Earth hor-ellipsis their history, their distribution hor-ellipsis their genetic hor-ellipsis connectionsclose quotes and is based on data on the abundance and distribution of elements obtained by various analytical methods. Neutron-activation analysis (NAA) plays a particular role in this respect. This is due to its high sensitivity (detection limit as small as 10 -14 g), which makes possible the use of samples of arbitrary mass, and also due to the possibility of obtaining information about composition without destruction of the object, conserving, if required, the unique material under investigation. Of the most interest are the data on the contents for a number of trace elements (at a level of 10 -7 - 10 -4 %), among which are rare-earth elements (REE), U, Th, Zr, Hf, Ta, W, Ga, Ni, Rb, Cs, platinum-group metals, Ag, Au, etc. These elements are considered as indicators of geochemical processes associated with the genesis and evolution of solar system bodies in early and more recent stages of evolution; they are also used to study processes and phenomena at zone boundaries: river-sea, ocean-atmosphere, and so on. The aim of this work is to show the capabilities of NAA in the determination of trace elements

  10. Determination of trace elements in tea by wavelength dispersive X-ray fluorescence spectroscopy

    International Nuclear Information System (INIS)

    Gong Chunhui; Zeng Guoqiang; Ge Liangquan; Li Jun; Wen Ziqiang

    2013-01-01

    Background: Measuring trace elements in tea can determine its nutritional value, verify the authenticity and place of origin, and detect the poisonous and harmful elements remaining in tea due to the application of chemical fertilizers and pesticides. Purpose: In order to reduce the time for sample preparation and the costs of equipment maintenance, wavelength dispersive X-ray fluorescence (WDXRF) spectroscopy was used to determine the trace elements in tea which is rapid, non-destructive and accurate. The contents of more than 20 elements can be measured simultaneously. Methods: Sample pieces were made by the sample preparation method of boric acid rebasing. To avoid the exogenous environmental pollution subjected in the growth of tea, we removed the residual dust of the tea by cleaning it. According to the principle that the standard samples should be similar types with the samples to be analyzed to select standard samples. The curves were built by SuperQ, which contained compiling the measurement conditions, establishing the measurement conditions, checking the angles, determining the measurement times, checking PHD and adding the contents and the names of sample pieces. The accuracy of the method can be obtained by comparing the measured values with the trace element contents of standard samples. The contents of trace elements in tea determined by WDXRF can be used to classify the tea attribution and the tea species through cluster analysis of SPSS software. Results: (1) The results show that the biggest relative standard deviation is 0.43% of Pb, and the precision is very good. (2) Five kinds of tea are taken separately in Fujian and Yunnan, measured three times with the established working curves. And tree diagram of cluster analysis can be obtained with SPSS software to analyze the measured average values with cluster analysis, coupling method between groups and Minkowski distance measurement techniques. It can be seen that in the tree diagram, when the

  11. The quantitative determination of trace elements in giant unicellular plants by particle-induced X-ray emission

    International Nuclear Information System (INIS)

    Navarrete-Dominguez, V.R.; Yoshihara, K.; Tanaka, N.

    1982-01-01

    Particle-induced X-ray emission (PIXE) was applied for the determination of trace elements in biologically interesting materials, giant unicellular plants. It was found that the PIXE method had advantages in multi-element trace analysis of a single cell of the sample plant. (author)

  12. Determination of trace elements in the reproduction systems of some rare animals using pixe

    Science.gov (United States)

    Suqing, Chen; Nengming, Wang; Jianxuan, Chen; Dazhong, Zhang

    In order to search for the significance of artificial feeding, reproduction and heredity, trace elements in the reproductive systems of some rare animals, including giant panda, lesser panda, marmot and river deer, have been determined. Typcial X-ray spectra of various samples are given. The elemental contents in ovary and testis of the giant panda and the lesser panda are calculated by means of yttrium as an internal standard. Elemental relative concentrations are calculated from peak areas in the spectra for thick samples. It is found that for the concentration of the elements Cr, Mn, Fe, Ni, Cu, As in the ovary there exist no significant different between the giant panda and the lesser panda. The concentration of Zn, however, shows a remakable difference. The importance of zinc in biological processes is discussed.

  13. Determination of trace and ultra-trace elements in Dergaon meteorite by inductively coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    Balaram, V.; Gnaneswara Rao, T.; Anjaiah, K.V.; Phukon, N.; Majumdar, A.C.

    2003-01-01

    In this paper, a detailed methodology for high precision measurement of several trace and ultra-trace elements including REE and PGE have been presented using effective sample preparation techniques and inductively coupled plasma mass spectrometry. Discussion is focussed on aspects, such as total dissolution and recovery of all elements, minimization of oxide and doubly-charged and other polyatomic ion interferences, calibration by matrix matching standards, accuracy and precision

  14. Activation analytical determination of essential and toxic trace elements in biological material

    International Nuclear Information System (INIS)

    Schelenz, R.

    1980-01-01

    In order to determine the essential trace elements Hg, Ag, Cu and Se in food (potatoes, milk powder) and biological standard materials (fruit tree leaves), simple, fast radiochemical separation methods are worked out. Following oxidative decomposition and destillation of Hg, the elements silver, copper and selenium are found in the destillation residue and can be electrochemically enriched on an amalgamated Cu foil (determination of Ag and Se in the concentration range of 10 -9 to 10 -8 g, of Cu in the range of 10 -12 to 10 -10 g), whilst the matrix elements Na, K, P are adsorbed on a column with 3 different inorganic ion exchangers. The eluate of the ion exchanger can be added directly to the multielement gamma spectroscopy. The possiblity of working purely instrumentally is demonstrated by 2 examples: multielement analysis of human hair and river water. (RB) [de

  15. Worldwide Interlaboratory Comparison on the Determination of Trace Elements in the IAEA-457 Marine Sediment Sample

    International Nuclear Information System (INIS)

    2016-01-01

    The primary goal of the IAEA Environment Laboratories is to assist Member States in the use of both stable and radioisotope analytical techniques to understand, monitor and protect the environment. In this context, the major impact of large coastal cities on marine ecosystems is an issue of primary concern for the IAEA and the IAEA Environment Laboratories. The marine pollution assessments required to understand such impacts depend on accurate knowledge of contaminant concentrations in various environmental compartments. Through the IAEA Environment Laboratories, the IAEA has been assisting national laboratories and regional laboratory networks since the early 1970s through the provision of a reference material programme for the analysis of radionuclides, trace elements and organic compounds in marine samples. Quality assurance and quality control are two fundamental requirements to ensure the reliability of analytical results. Data that are not based on adequate quality assurance and quality control can be erroneous, and their misuse can lead to poor environmental management decisions. In this regard, the IAEA has a long history of organizing interlaboratory studies, which have evolved to include an increasing array of potential contaminants in the marine environment. Relevant activities comprise global interlaboratory comparison, regional proficiency tests, the production of marine reference materials and the development of reference methods for trace elements and organic pollutants analysis in marine samples. This publication summarizes the results of the IAEA-457 interlaboratory comparison on the determination of trace elements in a marine sediment sample

  16. Trace Elements in the Conductive Tissue of Beef Heart Determined by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Wester, P.O.

    1965-08-01

    By means of neutron activation analysis, samples of four beef hearts taken from the bundle of His and adjacent ventricular muscle, the AV node and adjacent atrial muscle are investigated with respect to the concentration of 23 trace elements. The bulk elements K, Na and P are also determined. A recently developed ion-exchange technique, combined with subsequent γ-spectrometry, is used. The following trace elements are determined: Ag, As, Au, Ba, Br, .Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Hg, La, Mo, Rb, Sb, Sc, Se, Sm, W and Zn. In the conductive tissue compared to adjacent muscle tissue, calculations on a wet weight basis show a lower concentration of Cs, Cu, Fe, K, P, Rb and Zn in the former, and a higher concentration of Ag, Au, Br, Ca and Na. The mean differences (μg/g wet tissue), as well as their degree of significance, between the bundle of His and adjacent tissue from the ventricular septum, between the AV node and adjacent atrial muscle, between the ventricular septum and the right atrium, and between the bundle of His and the AV node are given for the elements Cu, Fe, K, Na, P and Zn

  17. Trace Elements in the Conductive Tissue of Beef Heart Determined by Neutron Activation Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Wester, P O

    1965-08-15

    By means of neutron activation analysis, samples of four beef hearts taken from the bundle of His and adjacent ventricular muscle, the AV node and adjacent atrial muscle are investigated with respect to the concentration of 23 trace elements. The bulk elements K, Na and P are also determined. A recently developed ion-exchange technique, combined with subsequent {gamma}-spectrometry, is used. The following trace elements are determined: Ag, As, Au, Ba, Br, .Ca, Cd, Ce, Co, Cr, Cs, Cu, Fe, Hg, La, Mo, Rb, Sb, Sc, Se, Sm, W and Zn. In the conductive tissue compared to adjacent muscle tissue, calculations on a wet weight basis show a lower concentration of Cs, Cu, Fe, K, P, Rb and Zn in the former, and a higher concentration of Ag, Au, Br, Ca and Na. The mean differences ({mu}g/g wet tissue), as well as their degree of significance, between the bundle of His and adjacent tissue from the ventricular septum, between the AV node and adjacent atrial muscle, between the ventricular septum and the right atrium, and between the bundle of His and the AV node are given for the elements Cu, Fe, K, Na, P and Zn.

  18. Report on intercomparison IAEA/W-4 of the determination of trace elements in simulated fresh water

    International Nuclear Information System (INIS)

    Pszonicki, L.; Hanna, A.N.; Suschny, O.

    1985-05-01

    The report presents results of a laboratory intercomparison on the determination of trace elements in simulated fresh water. 20 trace elements were analyzed by 38 laboratories from 21 countries. The results of the reported comparison confirm the agreement of the nominal concentration values of trace elements in the IAEA/W-4 simulated fresh water with the determined values of these elements. They also confirm that concentrated solutions of this type can be stored in quartz ampoules without any noticeable changes due to the adsorption of trace components on the quartz wall of vessels for considerable time. The concentration values of trace elements could be certified and the material IAEA/W-4 simulated fresh water issued as a reference material. 84% of all results were obtained either by atomic absorption or by atomic emission spectroscopy

  19. Determination of trace element contents in grass samples for cattle feeding using NAA techniques

    Energy Technology Data Exchange (ETDEWEB)

    Yusof, Alias Mohamad; Jagir Singh, Jasbir Kaur

    1987-09-01

    An investigation on trace elements contents in six types of grass samples used for cattle feeding have been carried out using NAA techniques. The grass samples, Mardi Digit, African Star, Signal, Guinea, Setaria and Setaria Splendida were found to contain at least 19 trace elements in varying concentrations. The results were compared to the figures obtained from available sources to ascertain the status as to whether the grass samples studied would satisfy the minimum requirements of trace elements present in grass for cattle feeding or otherwise. Preference made on the suitability of the grass samples for cattle feeding was based on the availability and abundance of the trace elements, taking into account factors such as the degree of toxicity, inadequate amounts and contamination due to the presence of other trace elements not essential for cattle feeding.

  20. Determination of trace element contents in grass samples for cattle feeding using NAA techniques

    International Nuclear Information System (INIS)

    Alias Mohamad Yusof; Jasbir Kaur Jagir Singh

    1987-01-01

    An investigation on trace elements contents in six types of grass samples used for cattle feeding have been carried out using NAA techniques. The grass samples, Mardi Digit, African Star, Signal, Guinea, Setaria and Setaria Splendida were found to contain at least 19 trace elements in varying concentrations. The results were compared to the figures obtained from available sources to ascertain the status as to whether the grass samples studied would satisfy the minimum requirements of trace elements present in grass for cattle feeding or otherwise. Preference made on the suitability of the grass samples for cattle feeding was based on the availability and abundance of the trace elements, taking into account factors such as the degree of toxicity, inadequate amounts and contamination due to the presence of other trace elements not essential for cattle feeding. (author)

  1. Determination of trace elements of Egyptian crops by neutron activation analysis Pt. 3

    International Nuclear Information System (INIS)

    Sherif, M.K.; Awadallah, R.M.; Amrallah, A.H.

    1980-01-01

    Multielemental neutron activation analysis was used for the determination of Al, As, Au, Br, Ca, Cd, Co, Cr, Cu, Fe, La, Mn, Mo, Sb, Se, W and Zn in African tea and lady's fingers (Malvaceae Family), ginger (Zingiperanceae Family), canella bark (Laureceae Family), black pepper (Piperaceae Family), cucumber seeds and vegetable marrow seeds (Cucurbitaceae Family), tomatos seed (Solanaceae Family), safflower seeds (Compositae Family), jew's mallow seed (Tiliaceae Family) and sesame (Pedaliaceae Family). Trace elements determination was made for the analysis of destructive (using super pure nitric acid and adsorbing the metal-APDC and metal-Dz complexes on activated charcoal) and nondestructive (dry seeds) samples. The method is simple, precise and sensitive for the determination of microamounts of the elements (ppm to ppb). (author)

  2. Determination of trace elements in acid rain by reversed phase extraction chromatography and neutron activation

    International Nuclear Information System (INIS)

    Rao, R.R.; Goski, D.G.; Chatt, A.

    1991-01-01

    A preconcentration neutron activation analysis (PNAA) method has been developed for the simultaneous determination of selected trace elements in acid rain and other water samples. The method consists of preconcentration of the elements by reversed phase extraction chromatography using oxine-loaded Amberlite XAD-2 resin. Nearly 100% recoveries were obtained for Co, Cu, Hg, V and Zn at pH 6.0 and for Cd at pH 7.0. Manganese gave incomplete recoveries at the pH range of 4.0-8.0 studies. Various factors that can influence preconcentration of the elements have been investigated in detail. The precision and accuracy of measurements have been evaluated by analyzing certified reference materials. The detection limits have been found to be of the order of ppb. The PNAA method has been applied to a number of acid rain and other water samples

  3. Determination of rare earths and traces of other elements by neutron activation analysis

    International Nuclear Information System (INIS)

    Atalla, L.T.; Mantovani, M.S.M.; Marques, L.S.

    A complete methodology for a multielemental analysis in geological material using the neutron activation technique was developed. 21 trace elements (9 of which are rare earths) were determined using thermal and epithermal neutron irradiations. Instrumetnal and radiochemical processing, applied to BCR-1 and G-2 geological standards, are described. Statistical tests carried out on G-2 data show an error smaller than 15% referring to all elements except Cr, Sb and Yb. The observed differences between are discussed. The good precision attained in this method is confirmed by its application to BCR-1 standard, which presents errors smaller than 4% for all elements except Nd, due to its intrinsic properties. The results from the present work are compared with those from other laboratories. (C.L.B.) [pt

  4. Determination of trace and toxic elements in Koran rice CRM by INAA, ICP and AAS

    International Nuclear Information System (INIS)

    Yong Sam Chung; Young Ju Chung; Kyung Haeng Cho; Joung Hae Lee

    1997-01-01

    Trace and toxic elements in Certified Reference Material (CRM) made of Korean rice at the Korea Research Institute of Standards and Science have been analyzed by Instrumental Neutron Activation Analysis (INAA). Data intercomparison from the measurement with those of Atomic Absorption Spectrometry (AAS) and Induced Coupled Plasma Spectrometry (ICPS) has been studied. The powdered samples were sterilized at 1.5 x 10 6 rad in the bottles using a 60 Co source after sieving and spiking to specific elements such as As, Cd, Cr, Cu and Hg and then the homogeneity of samples was assessed. Rice flour (SRM 1568a) and standard solutions made by the National Institute of Standards Technology (NIST) were used to construct the calibration curves for the INAA and the chemical methods, respectively. The uncertainties and concentration of constituent elements were determined and the possibility of their use for analytical quality control was considered. (author)

  5. Semi-quantitative spectrographic determination of traces of elements in igneous rocks

    International Nuclear Information System (INIS)

    Costa, M.Q. da; Eichhoff, H.-J.

    1982-01-01

    A semi-quantitative spectrographic technique based on Harveys'method, using background radiation as internal standard is described for the analysis of trace elements in igneous rocks by the total energy method. A certain amount of the sample was completely vapourized in a DC arc with anodic excitation under argon and oxygen atmosphere, using graphite electrodes of standard dimensions. In the processed film, selected lines and adjancent backgrounds were evaluated by densitometry and the corresponding intensity ratios were calculated. Sensitivity factors were determined for the analytical lines of Co, Cu, Ga, Ni, Sc, Sr, V, Y, Zn, and Zr in geological standards (G-2, BCR-1, AGV-1, GSP-1) from the United States Geological Survey. Matrix effects between samples and standards were minimized by using the above mentioned geological standards. An average value of the sensitivity factors was employed for the calculation of the concentration of the elements in the samples. A comparison between the results obtained by this method and those from the analysis of zinc by atomic absorption is presented. This method enabled the analyses of igneous rock samples having SiO2 contents between 40 and 80%, with an error in the determinations of trace elements less than 30%.(Author) [pt

  6. Th, U and trace elements determination in Egyiptian Lake sediments by INAA and laser fluorimetry

    International Nuclear Information System (INIS)

    Ismail, S.S.; Grass, F.; Ghods, A.

    1995-01-01

    A study was undertaken to determine element concentrations in Aswan High Dam Lake sediments. Sediment samples were collected from 40 to 500 km upstream of the dam to follow the sedimentation process and the distribution of Th, U and the trace elements in the lake. INAA was applied for the determination of Sm, Ce, Lu, Th, Cr, Yb, Au, Hf, Ba, Nd, Cs, Tb, Sc, Rb, Fe, Zn, Co, Eu, and Sb, while Laser Fluorimetry was applied for U determination. The accuracy and the reproducibility of the techniques were tested with IAEA standard materials (SL, Soil-7). The U values ranged from 4 ppm to 18 ppm, Th values were between 2 and 10 ppm, and showed a very good correlation with the rare earth elements and Fe. The distribution of most of the elements in the lake follows the same trend as the distribution of the clays in the sediments. Ba showed a negative correlation with most of the elements under investigation. (author) 5 refs.; 4 figs.; 7 tabs

  7. Determination of trace elements in fisheries samples by instrumental neutron and photon activation analysis

    International Nuclear Information System (INIS)

    Chattopadhyay, A.; Ellis, K.M.; Nimalasiri Desilva, K.

    1979-01-01

    An instrumental neutron activation analysis (INAA) method has been developed for the simultaneous determination of trace concentrations of up to 23 elements in fisheries samples. The INAA method consists of irradiations of wet and lyophilized cod muscle and liver samples for three different periods at a flux density of 5x10 11 n.cm -2 .s -1 and subsequent measurements after four different decay periods using high-resolution Ge(Li) gamma-ray spectrometry. Concentrations of several essential and toxic elements have been determined. Loss of certain elements during lyophilization has been studied. Elemental distribution in muscles and livers as a function of the age of fish has been investigated. Precision and accuracy of the INAA method have been evaluated by analysing replicate samples, National Bureau of Standards' bovine liver standard reference material, and an intercalibration fish flour sample provided by the International Council for the Exploration of the Sea. A few fish samples have also been analysed by an alternative method, namely instrumental photon activation analysis (IPAA). Elemental concentrations determined by both INAA and IPAA methods are reported here. (author)

  8. Solid-phase extraction and determination of trace elements in environmental samples using naphthalene adsorbent

    International Nuclear Information System (INIS)

    Pourreza, N.

    2004-01-01

    Naphthalene co-precipitated with quaternary ammonium salt such as tetraoctyl ammonium bromide and methyltrioctyl ammonium chloride have been used as adsorbent for solid phase extraction of metal ions such as Hg, Cd and Fe. The metal ions are retained on the adsorbent in a column as their complexes with suitable ligands and eluted by an eluent before instrumental measurements. The optimization of the procedures for solid phase extraction and consequent determination of trace elements and application to environmental samples especially water samples will be discussed. (author)

  9. A Fast Radiochemical Method for the Determination of Some Essential Trace Elements in Biology and Medicine

    International Nuclear Information System (INIS)

    Samsahl, K.

    1964-12-01

    A method has been developed for the determination with neutron-activation analysis of the following trace elements in soft biological tissues: Br, Ca, Cl, Cu, K, Mg, Mn, Mo, Na, P, Sr and Zn. The method consists in performing a short-term irradiation of the samples with a high thermal neutron flux, followed by fast chemical separations and gamma-spectrometric measurements. The chemical separations and the measurements of short-lived nuclides from a run are finished within 70 min, after the end of irradiation

  10. A Fast Radiochemical Method for the Determination of Some Essential Trace Elements in Biology and Medicine

    Energy Technology Data Exchange (ETDEWEB)

    Samsahl, K

    1964-12-15

    A method has been developed for the determination with neutron-activation analysis of the following trace elements in soft biological tissues: Br, Ca, Cl, Cu, K, Mg, Mn, Mo, Na, P, Sr and Zn. The method consists in performing a short-term irradiation of the samples with a high thermal neutron flux, followed by fast chemical separations and gamma-spectrometric measurements. The chemical separations and the measurements of short-lived nuclides from a run are finished within 70 min, after the end of irradiation.

  11. Liquid-Liquid Extraction and Determination of Trace Elements in Iron Minerals by Atomic Absorption Spectrometry

    International Nuclear Information System (INIS)

    Taseska, Milena; Stafilov, Trajche; Makreski, Petre; Jacimovic, Radojko; Jovanovski, Gligor

    2006-01-01

    Various trace elements (cadmium, chromium, cobalt, nickel, manganese) in some iron minerals were determined by flame (FAAS) and electrothermal atomic absorption spectrometry (ETAAS). The studied minerals were chalcopyrite (CuFeS 2 ), hematite (Fe 2 O 3 ) and pyrite (FeS 2 ). To avoid the interference of iron, a method for liquid-liquid extraction of iron and determination of investigated elements in the inorganic phase was proposed. Iron was extracted by diisopropyl ether in hydrochloride acid solution and the extraction method was optimized. Some parameters were obtained to be significantly important: Fe mass in the sample should not exceed 0.3 g, the optimal concentration of HCI should be 7.8 mol 1 -1 and ratio of the inorganic and organic phase should be 1: 1. The procedure was verified by the method of standard additions and by its applications to reference standard samples. The investigated minerals originate from various mines in the Republic of Macedonia. (Author)

  12. Determination of minor-and trace elements in magnesite samples, by activation analysis

    International Nuclear Information System (INIS)

    Sepulveda Munita, C.J.A.

    1979-01-01

    A method employing activation analysis with thermal neutron was developed for the determination of minor and trace elements in magnesite samples from the states of Ceara and Bahia (Brazil). Ten samples were analyzed. A qualitative analysis of the samples indicated the presence of Mn, Fe, Sc, Ca, Cu, Co and some of the lanthanides. The experimental part includes a non-destructive analysis of manganese and analysis with chemical separation of the other elements, individually or in groups, after sample dissolution, The dissolutions were made with concentrated HCl and the further separations were carried out in 8 N HCl medium. Iron was separated by means of an extraction of HFeCl 4 with isopropyl ether. Scandium and calcium were determined by retention of scandium with di-(2-ehylhexyl) phosphoric acid (HDEHP). The activities of 46 Sc and 47 Sc (a 47 Ca descendant) were employed for the analysis of scandium and calcium in the sample. In the effluent of the kieselguhr column copper and cobalt were determined, after retention in an anionic resin of the CuCl - 3 and CoCl - 3 complexes. Finally, in the effluent of the resin, the lanthanide group was separated by oxalate precipitation. In the gamma-ray spectrum of this precipitate the elements europium, cerium, samarium and lanthanum were determined. A detailed study of the possible interferences in the neutron activation analysis of the elements analysed was also made. The precision and accuracy of the results obtained and the sensitivity of the method are discussed. (Author) [pt

  13. Trace element determination in beauty products by k0-instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Sneyers, L.; Verheyen, L.; Vermaercke, P.; Bruggeman, M.

    2009-01-01

    A recent study on trace elements in beauty products and cosmetics sold on the Asian market has shown the presence of high levels of U, Th and rare earth elements in so called 'Hormesis cosmetics'. For the purpose of comparison, some more information about trace elements in European cosmetics would be useful. In this paper the results obtained using k 0 -standardised Instrumental Neutron Activation Analysis (k 0 -INAA) for more than 20 trace elements in 20 different beauty products collected from the European market are presented. We found traces of Ba, As and Sb which is in breach with European legislation. For some of the other elements like Cr and Co further speciation is needed in order to evaluate their presence in beauty products. (author)

  14. Intercomparison and determination of trace elements in urban dust by neutron activation analysis

    International Nuclear Information System (INIS)

    Chung, Yong Sam; Moon, Jong Hwa; Kim, Sun Ha; Park, Kwang Won; Kang, Sang Hun

    2000-01-01

    Trace elements in air samples artificially loaded on filters with urban dust and the bulk material of urban dust as an environmental sample were determined non-destructively using instrumental neutron activation analysis. Standard reference material (Urban Dust, SRM 1648) of the National Institute of Standard and Technology was used for the analytical quality control. The relative error for 37 elements was less than 15% and the standard deviation was less than 10%. 29 elements in the urban dust and 21 elements in the loaded filter sample were determined respectively. To evaluate the proficiency and reliability of the measurement, data intercomparison was performed and 39 analytical laboratories participated in the analysis using different analytical methods; neutron activation analysis, particle induced X-ray emission analysis, X-ray fluorescence analysis and atomic absorption spectrometry. Z-scores were calculated using the standard deviation of the laboratory's mean as target standard deviation, and a good result was obtained that the values fall between-1 and +1 except some elements. (author)

  15. Trace elements determinations in cancerous and non-cancerous human tissues using instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Choi, Insup.

    1989-01-01

    Recent improvements in analyzing techniques when coupled to the growing knowledge of trace element biochemistry provide a powerful tool to investigate the relationship between trace elements and cancer. It is hoped that selective delivery or restriction of specific minerals may aid in cancer prevention or treatment. Tissues were collected at the time of surgery of various cancer patients including colon cancer and breast cancer. Three kinds of tissues were taken from a patient; cancerous, noncancerous, and transitional tissue obtained from a region located between the cancer and healthy tissues. A total of 57 tissues were obtained from 19 cancer patients. Seven of them were colon cancer patients, and 5 of them were breast cancer patients. Nine elements were determined using instrumental activation analysis. Cancerous colon tissue had significantly higher concentrations of selenium and iron than healthy tissues. Cancerous breast tissue had significantly higher concentrations of selenium, iron, manganese, and rubidium than healthy tissues. Iron can be enriched in cancer tissue because cancer tissue retains more blood vessels. Selenium is enriched in cancer tissue, possibly in an effort of the body to inhibit the growth of tumors. The manganese enrichment can be explained in the same manner as selenium considering its suspected anticarcinogenicity. It is not certain why rubidium was enriched in cancer tissue. It could be that this is the result of alteration of cell membrane permeability, change in extracellular matrix, or increased metabolism in cancer tissue

  16. Abstracts book of 4. Poznan Analytical Seminar on Modern Methods of Sample Preparation and Trace Amounts Determination of Elements

    International Nuclear Information System (INIS)

    1995-01-01

    The 4. Poznan Analytical Seminar on Modern Methods of Sample Preparation and Trace Amounts Determination of Elements has been held in Poznan 27-28 April 1995. The new versions of analytical methods have been presented for quantitative determination of trace elements in biological, environmental and geological materials. Also the number of special techniques for sample preparation enables achievement the best precision of analytical results have been shown and discussed

  17. Selenium and Trace Element Distribution in Astragalus Plants: Developing a Differential Pulse Polarographic Method for Their Determination

    OpenAIRE

    SOMER, Güler; ÇALIŞKAN, A. Cengiz

    2007-01-01

    Astragalus plants have a wide range of applications in pharmaceuticals (gum tragacanth), as thickening agents in foods, and may have applications in controlling cancer cells. They are used as feed for animals and they are indicator plants for selenium. Because of their use in health-related areas it is very important to determine their selenium and trace element content with high accuracy. A new differential pulse polarographic method was established for trace element determination (...

  18. Trace element determination study in human hair by neutron activation analysis

    International Nuclear Information System (INIS)

    Frazao, Selma Violato

    2008-01-01

    Human hair analysis studies have been subject of continuous interest due to the fact that they can be used as an important tool to evaluate trace element levels in the human body. These determinations have been carried out to use hair for environmental and occupational monitoring, to identify intoxication or poisoning by toxic metals, to assess nutritional status, to diagnose and to prevent diseases and in forensic sciences. Although hair analysis presents several advantages over other human tissue or fluid analyses, such as organ tissue, blood, urine and saliva, there are some controversies regarding the use of hair analysis data. These controversies arise from the fact that it is difficult to establish reliable reference values for trace elements in hair. The purpose of this study was to evaluate the factors that affect element concentrations in hair samples from a population considered healthy and residing in the Sao Paulo metropolitan area. The collected human head hair was cut in small pieces, washed, dried and analyzed by neutron activation analysis (NAA). Aliquots of hair samples and synthetic elemental standards were irradiated at the IEA-R1 nuclear research reactor for 16 h under a thermal neutron flux of about 5x10 12 n cm -2 s -1 for As, Br, Ca, Co, Cr, Cs, Cu, Fe, K, La, Na, Sb, Sc, Se and Zn determinations. The induced gamma activities of the standards and samples were measured using a gamma ray spectrometer coupled to an hiperpure Ge detector. For quality control of the results, IAEA- 85 Human Hair and INCT-TL-1 Tea Leaves certified reference materials (CRMs) were analyzed. Results obtained in these CRMs presented for most of elements, good agreement with the values of the certificates (relative errors less than 10%) and good precision (variation coefficients less than 13.6%). Results of replicate hair sample analysis showed good reproducibility indicating homogeneity of the prepared sample. Results obtained in the analyses of dyed and non-dyed hair

  19. Determination of trace elements in tea leaves by neutron activation analysis

    International Nuclear Information System (INIS)

    Kasrai, M.; Shoushtarian, M.J.; Bozorgzadeh, M.H.

    1977-01-01

    Instrumental neutron-activation analysis has been employed to determine 14 trace elements in two brands of Iranian and foreign tea. A popular local brand (Ghoncheh) and a foreign brand (Lipton tea bags) were randomly purchased. The samples were dried in an oven (100 deg C) and used without further treatment. In order to measure the concentration of elements in tea solution, weighed amounts of tea were mixed with double-distilled boiling water. After cooling the leaves were separated by centrifugation. Aliquots of clear solution were dried for analysis. Three sets of standards containing the following elements using the spec-pure materials were prepared: (a) Cl, Mn, Na, K; (b) Br, La, Au; (c) Cr, Fe, Rb, Sc, Cs, Zn, Co. In each irradiation, one set of standards, along with the sample, was neutron irradiated at a thermal flux of approximately 2x10 13 ncm -2 sec -1 in the Research Reactor of the Nuclear Research Centre. The period of irradiation ranged from 10 min to 4 hrs, depending on the radionuclides to be measured. The transference ratio of the elements into solution, when tea is leached by percolation, is also reported. It was found that some elements are totally transferred into solution and some are partially retained by the leaves. (T.G.)

  20. Determination of trace elements in Turkish tea leaves by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Demiralp, R.

    1986-01-01

    The human body continuously assimilates a variety of inorganic elements from food and the environment. Some of these elements are closely related to human health and disorder. Tea is one of the most popular stimulating beverages which is consumed by low and high income family groups in many countries. Instrumental neutron activation analysis is one of the preferred methods because information on a large number of elements can be obtained simultaneously. Five packets each of the seven commonly used brands of tea were obtained from the market. In order to determine the transfer of trace elements into the drinkable portion about 2-3g. of the tea leaves were boiled in hot water for 2 min. After filtration the used tea leaves were dried at 65 deg. C in an oven and a portion, about 200mg was used for analysis. Samples and standards were irradiated 10 min. and 2 hrs. at pneumatic system and central thimble in the TRIGA MARK-II research reactor. After irradiation, the activities of samples and standards were measured with a aoaxial Ge detector coupled to a spectroscopic amplifier. A Canbera 90 model multi- channel analyzer with an 8K memory was used for pulse height analysis. The system has a resolution of 2.0 KeV. for the 1332.5 KeV gamma ray of 60 Co. The activity of the sample and standard was compared and the element contst of the sample was calculated. (author)

  1. Determination of trace elements and heavy metals in sediment using x-ray fluorescence

    International Nuclear Information System (INIS)

    Sidahmed, Muataz Ahmed Ibrahem

    2014-01-01

    In this study, 30 sediment samples were taken randomly from the area of Suba south of Khartoum state. Trace elements and heavy metal were determined in sediments samples using x-ray fluoresce spectroscopy (X RF). K, Ca, Ti, Mn, Fe, Cu, Zn, Pb, Rb, Sr, and Zr were determined by X RF. Standard Reference Material (SRM) from international Atomic Energy Agency (IAEA-Soil-7) has been used to achieve accuracy of X RF method. Measured values were found in agreements with certified values. The average elemental concentrations of K, Ca, Ti, Mn, Fe, Cu, Zn, Pb, Rb, Sr, and Zr were 5882.7, 20703.3, 6264.3, 460.97, 26713.3, 7.7, 43.4, 18.6, 28.6, 144.8, and 173.06, respectively. Correlation between elements was performed also cluster analysis was used to check the similarly between the samples result. The result of study were compared with previous studies and the concentrations of some elements found to be similar.(Author)

  2. Determination of trace elements in drinking water by neutron activation analysis

    International Nuclear Information System (INIS)

    Munita, C.S.; Abe, R.M.; Andrade e Silva, L.G. de.

    1988-10-01

    The concentracao of Hg, Cr, Zn, Fe and Co has been determined in fresh drinking water by a combination of preconcentration and neutron activation analysis. In order to preconcentrate the trace metals, a Chelex-100 resin in the NH + - form has been employed and it was not necessary to use special NH 4 + - form has been employed and it was not necessary to use special agents for the adsorption of the elements which are practically quantitatively retained by the resin. The retention of each element during the preconcentration was investigated using radioactive tracers. Selenium is known as a strongly interferent element for the analysis since the (n,Π) produced 75 Se has a Π-line at 0.279 MeV which coincides with the only Π-line of 203 Hg. The separation was made by a selective retention of mercury. After the sample had passed through the resin, the column was transfered to a polythylene envelope and irradiated at a neutron flux of about 5.10 12 ncm -2 s -1 for 8 h. For Hg the resin was irradiated in quartz ampoules. The samples were counted 15 days after the irradiation. The present method is superior to most other Chelex-100 separation procesures where elements of interest are eluted from the resin prior determinations thereby introducing the possibility of additional reagent blanks and incomplete as well as non-reproducible recoveries. (author) [pt

  3. Experimental determination of trace-element partitioning between pargasite and a synthetic hydrous andesitic melt

    Science.gov (United States)

    Brenan, J. M.; Shaw, H. F.; Ryerson, F. J.; Phinney, D. L.

    1995-10-01

    In order to more fully establish a basis for quantifying the role of amphibole in trace-element fractionation processes, we have measured pargasite/silicate melt partitioning of a variety of trace elements (Rb, Ba, Nb, Ta, Hf, Zr, Ce, Nd, Sm, Yb), including the first published values for U, Th and Pb. Experiments conducted at 1000°C and 1.5 GPa yielded large crystals free of compositional zoning. Partition coefficients were found to be constant at total concentrations ranging from ˜ 1 to > 100 ppm, indicating Henry's Law is oparative over this interval. Comparison of partition coefficients measured in this study with previous determinations yields good agreement for similar compositions at comparable pressure and temperature. The compatibility of U, Th and Pb in amphibole decreases in the order Pb > Th > U. Partial melting or fractional crystallization of amphibole-bearing assemblages will therefore result in the generation of excesses in 238U activity relative to 230Th, similar in magnitude to that produced by clinopyroxene. The compatibility of Pb in amphibole relative to U or Th indicates that melt generation in the presence of residual amphibole will result in the long-term enrichment in Pb relative to U or Th in the residue. This process is therefore incapable of producing the depletion in Pb relative to U or Th inferred from the Pb isotopic composition of MORB and OIB. Comparison of partition coefficients measured in this study with previous values for clinopyroxene allows some distinction to be made between expected trace-element fractionations produced during dry (cpx present) and wet (cpx + amphibole present) melting. Rb, Ba, Nb and Ta are dramatically less compatible in clinopyroxene than in amphibole, whereas Th, U, Hf and Zr have similar compatibilities in both phases. Interelement fractionations, such as DNb/DBa are also different for clinopyroxene and amphibole. Changes in certain ratios, such as Ba/Nb, Ba/Th, and Nb/Th within comagmatic suites may

  4. Determination of Trace Elements In Soil and Plants In Coastal Basin of Syria By Using Instrumental Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Kassem, A.

    2004-01-01

    Instrumental neutron activation analysis (INAA) methods have been used for the determination of some major, minor and trace elements (As, Cr, Co, Ni, Zn, Sb, Sc Ce, Ti, Fe, Mn and V) in some kinds of plant leaves with their soil. Accuracy of measurements have been evaluated by analyzing a number of plant and soil reference materials, precision have been estimated by triplicate the sample as well as the reference. The obtained accurate and reliable data in microgram quantities of some trace elements in plants and soil will serve as baseline values and will be helpful to monitor the changes in the trace elements content of soil and plant leaves. (Author)

  5. Report on the intercomparison run Soil-5 for the determination of trace elements in soil

    Energy Technology Data Exchange (ETDEWEB)

    Dybczynski, R; Tugsavul, A; Suschny, O

    1978-01-01

    he knowledge of the elemental composition of soil, and especially its trace element content is of interest to many investigators active in various fields of research. Among these concerned are not only agricultural chemists and soil scientists, but also biochemists, environmentalists, nutritionists and others. The increased recognition of the essentially on one hand and toxicity on the other, of certain trace elements towards animals and man, has led to intensified studies of the pathways of trace elements in nature, particularly in the environmental research. Not only atmosphere, hydrosphere and biological tissues, but also soil is examined. Essential and toxic trace elements may pass from soil to plants (by which they are sometimes effectively concentrated) and further through food chains to Man. The interest in the analysis of soil for the content of many trace and also some major elements is therefore rapidly increasing. Hence, there seems to be an obvious need for a reference material with established 'recommended values' of as many elements as possible which could be used for checking the quality of analytical work of the laboratories engaged in soil analyses. At the same time well-characterized soil, containing high levels of minerals can be also of interest for geochemists as a complement to already existing geochemical reference samples.

  6. The spectrographic determination of minor and trace elements in copper, lead, and zinc concentrates

    International Nuclear Information System (INIS)

    Breckenridge, R.L.; Russell, G.M.; Watson, A.E.

    1976-01-01

    This report deals with the development of a method for the determination, by an emission-spectrographic technique, of magnesium, manganese, aluminium, silver, calcium, chromium, cobalt, titanium, antimony, cadmium, molybdenum, zirconium, nickel, boron, vanadium, arsenic, beryllium, tin, germanium, and bismuth in copper, lead, and zinc sulphide concentrates. The method involves the preparation of complex standards in which the volatile elements arsenic, antimony, cadmium, tin, and bismuth are incorporated as sulphide compounds at temperatures of 800 degrees Celsius in evacuated silica tubes together with a synthetic sulphide matrix. These standards are then mixed with the other minor and trace elements to form composite standards. The conditions for excitation with a direct-current arc, and the analytical lines for the elements and internal standards, are given. The procedure is rapid and convenient, and involves the minimum of sample preparation. The accuracy is about 10 per cent, and the method has a coefficient of variation for the various elements of between 2 and 13 per cent

  7. Application of neutron activation analysis to trace element determinations in lung samples

    International Nuclear Information System (INIS)

    Rocero, Sizue Ota

    1992-01-01

    The purpose of this work was to apply the instrumental neutron activation analysis method to determine trace elements in lung samples from smokers and non smokers. Samples of lung tissues and lymph nodes from pulmonary hilum analyzed were collected from autopsies by researchers from the Medicine College of the University of Sao Paulo, SP, Brazil. Adequate conditions for preparation and analysis of samples were previously established. The preparation of samples consisted of homogenization, lyophilization and sterilization in 60 Co source. The samples and standards were irradiated in the IEA-R1 reactor under thermal neutron flux of 3.7 x 10 11 n.cm -2 .s -1 for 30 min to determine Cl, K, Mn and Na and for 16 h under flux of 10 19 n.cm -2 .s -1 for the determination of Au, Br, Ce, Co, Cr, Cs, Eu, Fe, Hf, La, Rb, Sb, Sc, Se, Th and Zn. The counting were carried out with a hiperpure (ge) detector connected to a 4096 channels analyzer and a microcomputer. the results obtained for lung sample analyses indicated a good reproducibility of the method for most of the elements determined with relative standard deviations lower than 10.5%. The accuracy of the method was evaluated by analyzing reference materials such as IAEA Animal Muscle H-4, NIST Bovine Liver 1577a, IUPAC Bowen's Kale and NIES Vehicle Exhaust Particulates. The results obtained from these analyzes agreed with the values of the literature for several elements with relative errors less than 20%. Less precise and accurate results were obtained for elements with concentrations at the Mup/Kg levels. Elemental concentrations obtained in the lung tissue analyses were within the range of reference values for normal subjects presented in the literature, except for the Cl concentrations for non smokers, Hf in both groups and Sb for the smokers. By comparing results obtained for lung samples from smokers and non smokers, the concentrations of Ce, Cr and Sb were higher in lungs from smokers and the others elements were

  8. Determination of arsenic and other trace elements in cosmetics by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Gonzalez Cepeda, A.M.; Cienfuegos Silva, E.E.

    1978-01-01

    A general survey of trace-elements in different types of cosmetics, in particular arsenic, was carried out in order to detect elements that might be detrimental to human health. The samples were analyzed by instrumental neutron activation analysis and high-resolution gamma-ray spectrometry with Ge(Li) detectors. Different amounts of Br and Sb, detected in almost all the samples, produced interferencies in the determination of As when the 559 KeV photopeak was used. Since the triplet formed could not be resolved by the Ge(Li) detector, a mathematical procedure was developed using the 776 KeV gamma-ray emission of 82-Br and various factors found experimentally. This procedure was checked using laboratory-made samples of known concentrations and the results obtained had good precision and accuracy. In addition to arsenic the elements Co, Cr, Br, Sc, Fe and Zn were also quantitatively determined. Those cosmetics made from inorganic raw materials have an As concentration higher than those elaborated from organic materials. (EC)

  9. Trace elements determination in Syrian honey using x-ray fluorescence technique

    International Nuclear Information System (INIS)

    Khuder, A.; Ahmad, M.; Saour, G.

    2009-05-01

    Major and trace elements of S, Cl, K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Rb, Sr in 27 Syrian honey samples, which collected from different areas in the country, in addition to 3 imported honey samples, were determined by dry ashing method for XRF analysis. The samples were diluted and homogenized with a binder made from cellulose powder. The analyzed elements were divided into three groups, relating to the secondary targets used for X-ray excitation. The internal standard method for XRF analysis with a Mo secondary target was used for the determination of the first group of elements: Sr, Rb, Se, As, Zn, Cu, Ni, and Fe. While, the external standard method for XRF analysis with Cu and Ti secondary targets was used for the determination of the second: Mn, Cr, Ti, Ca, K, and third: Cl, and S group of elements, respectively. The results were accurate with a relative standard error less than 4.2 %. The problem of element loss was overcome by the complete drying of honey samples before their ashing. The moisture content was obtained using mass loss and refractive index methods. As a result, the lower limits of detection (LLD) obtained by Mo-XRF was in the range from 0.011 μg Sr/g to 0.064 μg Fe/g, resulting for samples containing 0.1 % ash and collecting live time 1000 s; while, LLD obtained by Cu-XRF was in the range 0.014 μg Mn/g to 0.057 μg K/g. LLD for S and Cl using Ti secondary target was with values of 0.503 μg/g and 1.96 μg/g, respectively. The enhancement factor obtained by drying method for XRF was in the range from 147 to 1667. Normal concentration of elements in Syrian honey was obtained. The concentration of elements was comparable to those obtained by other workers for honeys in different countries. Elements of K, Ca, and Cl were predominantly distributed in all Syrian honey samples. Elements of Sr, Zn, Cu, Fe, Ti, and S were well distributed in all honey samples. While, the concentrations of Rb, Ni, Mn, Cr elements in some honey samples were below the

  10. Determination of essential trace elements in wine by neutron activation analysis

    International Nuclear Information System (INIS)

    Daniele, Anna Paula

    2016-01-01

    Several studies have been carried out for determining essential elements in foodstuffs, including wine, due to its important nutritional role in human body functions. It was shown that daily consumption of wine in moderation contributes significantly to the needs of essential elements in human body such as Ca, Co, Cr, Fe, K, Mg, Mn, Zn, V, among others, and has health benefits in the prevention of numerous diseases and longer life expectancy, related in particular to the intake of antioxidants such as polyphenolic compounds. Trace elements are good indicators of origin of wines and their concentrations can be used as criteria to ensure authenticity, quality and show that the tolerance limits established by law were respected throughout the production process. However, although Brazilian wine industry is among the 15 largest in the world, analytical studies for organic and inorganic compounds of wine content are still small when compared to other major producers. In this sense, this study aimed to evaluate some procedures of wine sample preparation to determine essential elements by Instrumental Neutron Activation Analysis (INAA) and compare the results with those determined by Inductively Coupled Plasma Atomic Emission Spectrometry (ICP OES). Three sample preparation procedures were studied: freeze-drying, evaporation and dry ashing. The parameters studied were precision, accuracy and detection limit. ANOVA and Tukey-Kramer tests were applied to verify the statistical differences between the mean values obtained by the three wine preparation procedures for INAA with those means obtained by ICP OES. It was noticed that about 60% of results obtained by freeze-drying agreed with those obtained by ICP OES. (author)

  11. (F)UV Spectroscopy of K648: Abundance Determination of Trace Elements

    Science.gov (United States)

    Mohamad-Yob, S. J.; Ziegler, M.; Rauch, T.; Werner, K.

    2010-11-01

    We present preliminary results of an ongoing spectral analysis of K 648, the central star of the planetary nebula Ps 1, based on high resolution FUV spectra. K 648, in M 15 is one of only four known PNe in globular clusters. The formation of this post-AGB object in a globular cluster is still unclear. Our aim is to determine Teff, log g, and the abundances of trace elements, in order to improve our understanding of post-AGB evolution of extremely metal-poor stars, especially PN formation in globular clusters. We analyzed FUSE, HST/STIS, and HST/FOS observations. A grid of stellar model atmospheres was calculated using the Tübingen NLTE Model Atmosphere Package (TMAP).

  12. Determination of minor and trace elements in kidney stones by x-ray fluorescence analysis

    Science.gov (United States)

    Srivastava, Anjali; Heisinger, Brianne J.; Sinha, Vaibhav; Lee, Hyong-Koo; Liu, Xin; Qu, Mingliang; Duan, Xinhui; Leng, Shuai; McCollough, Cynthia H.

    2014-03-01

    The determination of accurate material composition of a kidney stone is crucial for understanding the formation of the kidney stone as well as for preventive therapeutic strategies. Radiations probing instrumental activation analysis techniques are excellent tools for identification of involved materials present in the kidney stone. In particular, x-ray fluorescence (XRF) can be very useful for the determination of minor and trace materials in the kidney stone. The X-ray fluorescence measurements were performed at the Radiation Measurements and Spectroscopy Laboratory (RMSL) of department of nuclear engineering of Missouri University of Science and Technology and different kidney stones were acquired from the Mayo Clinic, Rochester, Minnesota. Presently, experimental studies in conjunction with analytical techniques were used to determine the exact composition of the kidney stone. A new type of experimental set-up was developed and utilized for XRF analysis of the kidney stone. The correlation of applied radiation source intensity, emission of X-ray spectrum from involving elements and absorption coefficient characteristics were analyzed. To verify the experimental results with analytical calculation, several sets of kidney stones were analyzed using XRF technique. The elements which were identified from this techniques are Silver (Ag), Arsenic (As), Bromine (Br), Chromium (Cr), Copper (Cu), Gallium (Ga), Germanium (Ge), Molybdenum (Mo), Niobium (Nb), Rubidium (Rb), Selenium (Se), Strontium (Sr), Yttrium (Y), Zirconium (Zr). This paper presents a new approach for exact detection of accurate material composition of kidney stone materials using XRF instrumental activation analysis technique.

  13. Determination of trace elements and screening of metalloproteins in human blood and tissues

    International Nuclear Information System (INIS)

    Prohaska, K.

    2003-02-01

    ). For the very low concentrations of trace element in blood fractions (e.g. Co, Cr, or Ni) the GFAAS had to be used. The simultaneous ICP-OES was applied for the determination of Ca, Mg, P, Fe, Cu, and Zn in whole blood. Line selection was performed in the complex sample matrix. In digested freeze-dried blood the simultaneous lines showed no interferences for Ca, Cu, Fe, Mg, P, S, and Zn. Only for Co serious interference occurred in the matrix. The method was not suitable for the determination of Cd, Cr, Mn, Mo, Nb, Ni, Pb, Ti, and V in the blood samples, because the LODs of the ICP-OES method were too high for this purpose. (author)

  14. Studies of trace element determinations in nails by neutron activation analysis method

    International Nuclear Information System (INIS)

    Aguiar, Amilton Reinaldo; Saiki, Mitiko

    1996-01-01

    The purpose of this work was to develop the neutron activation analysis for trace element determinations in nails in order to apply this method to the study of the cystic fibrosis disease. It was verified that the elements Al, As, Br, Ca, Cd, Cl, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Se and Zn can be determined by using short and long irradiations with thermal neutron flux from 10 11 to 10 13 n.cm -2 . -1 at the IEA-R1 nuclear research reactor. The washing solutions of triton-X100, NH 4 OH and acetone were tested in order to eliminate external contaminants from the nail samples. The nail analyses of the individual fingers from both of hands showed that the samples must be collected from all the fingers from both of hands to have a representative sample. The precision and the accuracy of the results were also examined by analyzing NIES 10C Rice Flour, IUPAC Bowen's Kale and NIST 1572 Citrus Leaves reference materials. (author)

  15. Principle of neutron activation analysis and its use for determination of trace elements in sediment

    International Nuclear Information System (INIS)

    Verma, Rakesh

    2012-01-01

    information. Their chemical characterization is needed to understand the natural and anthropogenic influence on the bodies of water. Nuclear analytical techniques such as NAA and X-ray fluorescence spectrometry (XRF) have been used for determination of various elements in sediment. Recently we have participated in the inter-laboratory comparison organized by International Atomic Energy Agency for the determination of trace elements in sediment sample. The results of analysis will be discussed. (author)

  16. The use of nuclear related analytical techniques for the determination of ingestion and body content of trace elements

    International Nuclear Information System (INIS)

    Djojosubroto, H.; Santoso, D.; Widjajakusuma, B.

    1998-01-01

    A number of observations revealed that various human disease states are associated with measurable abnormalities of trace element levels. Until present there is no data on trace element levels in human tissues and dietary intake representing the population in Indonesia. Trace element level in various biological materials, especially human serum related to health syndrome (e.g. acute myocardial infarction and goiter prevalences) was performed by National Atomic Energy Agency in cooperation with relevant institutes. The present study is concerned with determination of ingestion and organ content of trace elements of importance in radiological protection (Cs, Sr, I, Th and U). Quantitation of the elements in the samples will be determined by neutron activation analysis, complemented by nuclear related analytical techniques, e.g. inductively coupled plasma - mass spectrometry and atomic absorption spectrometry. Samples to be analyzed consist of (a) total diets and individual staple foodstuffs, (b) autopsy specimens of liver, lung, kidney, muscle, thyroid and bone, and (c) drinking water. It seems difficult for us to define nationally representative specimens of total diets and individual staple foodstuffs. Based on these facts, in the first year activity samples of dietary intake from various socio economic levels of population in West Java will be collected. Human tissue sample is obtained from autopsy of normal persons who are killed in traffic accident or homicide victim. Traces of Th and U in drinking water are determined by neutron activation analysis following preconcentration of these elements in chelating resin Chlelex 100. (author)

  17. Neutron activation analysis applied to the determination of trace elements in human nails

    International Nuclear Information System (INIS)

    Aguiar, Amilton Reinaldo

    2001-01-01

    There is a considerable interest in the determination of trace elements in human nails in order to use this tissue as a monitor of nutritional and healthy status of individuals, of occupational exposure diseases and of the environmental contamination. In this work, instrumental neutron activation analysis was applied to determine trace elements in finger nail clippings to make comparisons between the elemental concentrations obtained in nails from healthy individuals of a control group and those from cystic fibrosis (CF) patients. Firstly, a protocol for sample collection and preparation for analysis was established. Finger and toe nail samples from CF patients were collected at the Instituto da Crianca of Medicine School, University of Sao Paulo, SP. The nail samples from control group were collected from healthy adults and from children living in Sao Paulo city, SP. These samples were cleaned by stirring them witha a diluted Triton X100 solution and then by washing with distilled water and acetone. The analytical procedure consisted of irradiation nail samples and elemental standards in the IEA-R1m nuclear reactor under thermal neutro flux of about 10 12 n cm -2 s -1 , for short and long period irradiations. The activities of the radionuclides were measured using a gamma-ray spectrometer comprising an hyperpure Ge detector and associated electronic system. The biological reference materials Bovine Liver 1577b and Oyster Tissue 1566a, both from National Institute of Standards and Technology, USA were analysed in order to evaluate the accuracy and precision of the results. The analysis of variance (ANOVA) and F-test at the significance level of 5% were used to make a comparison between the sets of results obtained in this work. In the comparison of the results obtained for finger and toe nails from CF patients, the Br concentrations were higher in finger nails that those obtained for toe nails. For the control group of children, the finger nails presented different

  18. Optimization of trace elements determination (Arsenic and chromium) in blood and serum of human by electrothermal atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Ahmadi Faghih, M. A.; Aflaki, F.

    2003-01-01

    Trace elements play an important role in the bio physiology of cells by affecting their growth and contributions to various biological processes such as wound healing. Determination of toxic trace elements in biological fluids is an important subject of interest for toxicological purposes. Increasing the concentration of these elements in the blood levels, cause serious diseases in patients. Recently instrumental analysis procedures such as atomic absorption spectrometry have been used in clinical measurements for determination of many toxic trace elements in the biological samples. In this paper we are reporting the study of various methods of blood and serum samples preparation for determining the toxic trace elements of Arsenic and Chromium. The measurement of this elements performed by using electrothermal atomic absorption spectrometry. The best and reliable results for Chromium analysis was achieved by injection of diluted serum samples, where the samples were diluted with H CI 0.1N. In Arsenic analysis, the best results obtained by extraction with aqueous solution of TCA. For determining all of these elements the RSD% was less than 5%

  19. Development of a procedure for the multi-element determination of trace elements in wine by ICP-MS

    Energy Technology Data Exchange (ETDEWEB)

    Castineira, M.M.; Brandt, R.; von Bohlen, A.; Jakubowski, N. [Institut fuer Spektrochemie und Angewandte Spektroskopie e.V., Dortmund (Germany)

    2001-07-01

    An inductively coupled plasma mass spectrometric (ICP-MS) procedure has been developed for the determination of trace elements in wine. The procedure consists in simple 1+1 dilution of the wine and semi-quantitative analysis (without external calibration) using In as internal standard. Thirty-one elements at concentrations ranging from 0.1 mg mL{sup -1} to 0.5 ng mL{sup -1} can be determined by ICP-MS analysis with and without digestion. It was investigated whether a matrix effect observed for EtOH in the wine matrix can be overcome by application of a micro-concentric nebulizer with a membrane desolvator (MCN 6000). The results obtained for the MCN 6000 are compared with those obtained by use of a conventional Meinhard nebulizer. It is shown that the observed matrix effect can only be compensated by use of an internal standard for the Meinhard nebulizer, but not for the MCN 6000. Results for ICP-MS are compared with those obtained by total reflection X-ray fluorescence spectrometry (TXRF). (orig.)

  20. Report on intercomparison IAEA/V-10 of the determination of trace elements in hay powder

    International Nuclear Information System (INIS)

    Pszonicki, L.; Hanna, A.N.

    1985-07-01

    Hay plays an important role in the natural production circle of human nutrition. The level of its pollution is an important factor which can effect various branches of the food industry. The aim of the reported exercise organized by the IAEA was to provide the participating laboratories an opportunity to check their analytical performance by comparing their results with the results of other laboratories and to establish the concentration level of trace elements for certification purposes. The hay powder was analyzed by 50 laboratories from 25 countries for 42 elements. Neutron activation, atomic absorption, atomic emission and X-ray spectroscopy were predominantly used as analytical methods. The results provided by the participants of the reported intercomparison exercise have enabled to certify the concentration of eighteen trace and minor elements and to establish non-certified information values for the concentration of an additional twelve elements in Hay Powder IAEA/V-10

  1. Report on intercomparison V-9 of the determination of trace elements in cotton cellulose

    International Nuclear Information System (INIS)

    Pszonicki, L.; Hanna, A.N.; Suschny, O.

    1983-03-01

    Trace elements in plants are being investigated in many laboratories using nuclear techniques, mainly neutron activation analysis. To enable these laboratories to check the accuracy of their work and to provide data needed in the certification of a batch of reference material, the IAEA has organized several intercomparisons of analytical results of plants. This report deals with the comparative evaluations of the results on cotton cellulose powder. A total of 27 laboratories from 19 countries submitted 377 laboratory means on 57 elements

  2. Survey of currently available reference materials for use in connection with the determination of trace elements in biological materials

    International Nuclear Information System (INIS)

    Parr, R.M.

    1983-09-01

    Elemental analysis of biological materials is at present the subject of intensive study by many different research groups throughout the world, in view of the importance of these trace elements in health and medical diagnosis. IAEA and other organizations are now making a variety of suitable reference materials available for use in connection with the determination of trace elements in biological materials. To help analysts in making a selection from among these various materials, the present report provides a brief survey of data for all such biological reference materials known to the author. These data are compiled by the author from January 1982 to June 1983

  3. INAA for the determination of trace elements and evaluation of their enrichment factors in lichens of high altitude areas

    International Nuclear Information System (INIS)

    Bergamaschi, L.; Rizzio, E.; Giaveri, G.; Profumo, A.; Gallorini, M.; Giordani, L.

    2005-01-01

    Trace element (TE) characterization and analysis in epiphytic lichens collected in different areas of the Himalayas (Nepal) and of the Alps (Italy) is presented. The results give information for the assessment of TE distribution present in the two different areas. The evaluation of the enrichment factors may provide information for many elements about their association to long-distance atmospheric transport phenomena. To this purpose, samples of superficial soils, collected in the same areas of those of the lichens, have also been analyzed. Most of the trace elements were determined by instrumental neutron activation analysis (INAA), while lead and cadmium measurements were carried out with electrothermal atomic absorption spectroscopy (ET-AAS). (author)

  4. Accelerator SIMS, a technique for the determination of stable trace elements in ultrapure materials

    Energy Technology Data Exchange (ETDEWEB)

    Ender, R.M.; Suter, M. [Eidgenoessische Technische Hochschule, Zurich (Switzerland); Doebeli, M.; Synal, H.A. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-09-01

    A new sputtering chamber with special precautions against sample contamination from the surroundings of the sample has been added to the AMS beamline of the tandem accelerator. This allows the detection of trace element concentrations in ultrapure materials below the ppb range in many cases. (author) 1 fig., 2 refs.

  5. Comparison of three analytical methods for the determination of trace elements in whole blood

    International Nuclear Information System (INIS)

    Ward, N.I.; Stephens, R.; Ryan, D.E.

    1979-01-01

    Three different analytical techniques were compared in a study of the role of trace elements in multiple sclerosis. Data for eight elements (Cd, Co, Cr, Cu, Mg, Mn, Pb, Zn) from neutron activation, flame atomic absorption and electrothermal atomic absorption methods were compared and evaluated statistically. No difference (probability less than 0.001) was observed in the elemental values obtained. Comparison of data between suitably different analytical methods gives increased confidence in the results obtained and is of particular value when standard reference materials are not available. (Auth.)

  6. Determination of trace elements in airborne particulates by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Jung, Yong Sam; Jung, Yung Joo; Jung, Eui Sik; Cho, Seung Yun

    1995-01-01

    Trace elements in airborne particulates were analyzed by instrumental neutron activation analysis(INAA) under the optimum analytical condition. Neutron irradiation for sample was done at the irradiation hole(neutron flux, 1 x 10 13 n/cm 2 s) of TRIGA MARK-III research reactor in the Korea Atomic Energy Research Institute. For the verification of the analytical method, NIST SRM-1648 and NIES CRM No.8 were chosen and analyzed. The accuracy and precision of the analysis of 40 and 24 trace elements in the samples were compared with the certified and reported values, respectively. The analytical method was found to be reliable enough when the analytical data of NIES sample were compared with those of different countries. In the analytical result of two or both of standard reference materials, relative standard deviation was within the 15% except a few elements and the relative error was within the 10%. We used this method to analyze 30 trace elements in airborne particulates collected with the high volume air sampler(PM-10) at two different locations and also confirmed the possibility to use this method as a routine monitoring tool to find out environmental pollution sources. 3 figs., 8 tabs., 19 refs. (Author)

  7. Minerals and trace elements determination in diets by neutron activation analysis

    International Nuclear Information System (INIS)

    Eiras, Maria Izabel O.; Favaro, Debora I.T.; Ribeiro, Marisilda; Cozzolino, Silvia M.F.

    2002-01-01

    In the present study 12 diets, each one consisting of a pool of seven day diets, composed by four meals: breakfast, lunch, dinner and snack, adequate in energy and macro nutrients according to the RDA (Recommended Daily Allowance) recommendations, were elaborated and offered to a group of 12 men (19-42 years). The diets were collected by duplicate portion technique and dried by two different processes: freeze drying and 60 deg C ventilated oven drying. In the total, 24 diets were analyzed. The content of some minerals and trace elements (Ca, Fe, Mg, Mn, Na, Se and Zn) were determined by Instrumental Neutron Activation Analysis. The validation of methodology was made by analysis of the reference materials Typical Diet (NIST SRM 1548 a ), Orchard Leaves (NIST SRM 1541) and Peach Leaves (NIST SRM 1547). The results observed by two different drying processes used were statistically compared by test T of Student. It was possible to conclude that the concentration means can be considered as statistically equal, within a significance level of 0.05. The daily intake values calculated from the concentration results were: 712 (± 59) mg Ca/day; 10.7 (± 0.8) mg Fe/ day; 3387 (± 16) mg K/ day; 275 (± 6) mg Mg/ day; 3.0 (± 0.5) mg Mn/ day; 3656 (± 699) mg Na/ day; 42 (± 6) μg Se/ day e 11.6 (± 2.4) mg Zn/ day. The calculated intake was compared to the new daily recommended values set by RDA (National Research Council-USA) for the range age of individuals studied. It was possible to conclude that the diets were adequate in Fe and Zn and inadequate for the other elements. Concerning the minerals Na and K we verified high daily intake levels and this was already observed in other Brazilian regional diets. (author)

  8. Official Methods for the Determination of Minerals and Trace Elements in Infant Formula and Milk Products: A Review.

    Science.gov (United States)

    Poitevin, Eric

    2016-01-01

    The minerals and trace elements that account for about 4% of total human body mass serve as materials and regulators in numerous biological activities in body structure building. Infant formula and milk products are important sources of endogenic and added minerals and trace elements and hence, must comply with regulatory as well as nutritional and safety requirements. In addition, reliable analytical data are necessary to support product content and innovation, health claims, or declaration and specific safety issues. Adequate analytical platforms and methods must be implemented to demonstrate both the compliance and safety assessment of all declared and regulated minerals and trace elements, especially trace-element contaminant surveillance. The first part of this paper presents general information on the mineral composition of infant formula and milk products and their regulatory status. In the second part, a survey describes the main techniques and related current official methods determining minerals and trace elements in infant formula and milk products applied for by various international organizations (AOAC INTERNATIONAL, the International Organization for Standardization, the International Dairy Federation, and the European Committe for Standardization). The third part summarizes method officialization activities by Stakeholder Panels on Infant Formula and Adult Nutritionals and Stakeholder Panel on Strategic Food Analytical Methods. The final part covers a general discussion focusing on analytical gaps and future trends in inorganic analysis that have been applied for in infant formula and milk-based products.

  9. Vertical distribution of particulate trace elements in a street canyon determined by PIXE analysis

    International Nuclear Information System (INIS)

    Raunemaa, T.; Hautojaervi, A.; Kaisla, K.; Gerlander, M.

    1981-01-01

    Suspended particles in a street canyon were investigated by collecting air particulate matter on thin filters at heigths 2.3 to 20.5 m. The weather parameters and traffic characteristics were registered during the collection. Quantitative analysis of 15 trace elements from AI to Pb was carried out by the PIXE method using 1.8-2.0 MeV protons. The concentration of lead was found to decrease exponentially when going from street level to roof level. Almost all the trace elements analyzed were found to fall into two groups with different vertical distributions. The collected matter above 10 m height was found to be due mainly to combustion originated motor vehicle exhaust, the matter below 10 m to soil originated dust. (orig.)

  10. Analytical determination of traced elements in concrete samples used in nuclear reactors of the European Community

    International Nuclear Information System (INIS)

    May, S.; Piccot, D.

    1984-01-01

    In reactor dismantling residual radioacting of concrete used, especially in biological shield can brought problems for treatment and disposal. Radioactivity of concrete from reactors can be forecasted if element content is known. Elements producing long life radionuclides are: chlorine, calcium nickel, cobalt, niobium, europium and samarium. Neutron activation analysis is used for determination of these elements whithout chemical separation for Ca, Co, Eu and Sm and with radiochemical separation for Cl, Ni and Nb. A lot of elements, less interesting are also determined by gamma spectrometry after irradiation. It was possible to determine 29 elements in 21 concrete samples from different European Community reactors

  11. Determination of trace elements in a cigarette paper by neutron activation analysis

    International Nuclear Information System (INIS)

    Abedinzadeh, Z.; Khalkhali, Zh.; Razeghi, M.; Parsa, B.

    The concentration of 19 trace elements in a cigarette paper (Zig-Zag Paper Company, France) which is used in making different brands of Iranian cigarettes, has been measured by neutron activation analysis, employing a high-resolution Ge(Li) detector. They include Na, K, Ca, Sc, Cr, Mn, Fe, Co, Zn, Br, Sr, Sb, Ba, Ce, Eu, Gd, Au, Hg, and Th. (author)

  12. Trace element determination in fingernails, hair and blood serum in patients with Crohn's disease using neutron activation analysis

    International Nuclear Information System (INIS)

    Buschmann, H.

    1984-01-01

    The determination of trace elements and electrolyte concentrations in blood serum, hair and fingernails of 16 patients with Crohn's disease was carried out by means of instrumental neutron activation analysis. In the serum a significant decline in the zinc content could be registered, while the remaining trace elements remained in the normal range. The parenteral nutrition also showed a zinc deficiency. There was, however, also an iron deficiency. The studies of the hair and fingernails gave the following results: Rubidium and antimony in the normal range; zinc, selenium, iron and cobalt below normal values. (orig./PW) [de

  13. Determination of trace elements in soil and plants in the Orontes basin of Syria by using instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Kassem, A.; Sarheel, A.; Al-Somel, N.

    2004-01-01

    Instrumental neutron activation analysis (INAA) have been used for the determination of some major, minor and trace elements (As, Cr, Co, Ni, Zn, Sb, Sc, Ce, Ti, Fe, Mn and V) in various plant leaves together with their soil. The accuracy of the measurements have been evaluated by analyzing a number of plant and soil reference materials, precision have been estimated by triplicate analysis of the sample as well as that of the reference material. The obtained accurate and reliable data of some trace elements on microgram level for plants and soil will serve as baseline values and will be helpful to monitor the changes in the trace element content of soil and plant leaves. (author)

  14. The determination of trace elements in new food grain SRM's using neutron activation analysis

    International Nuclear Information System (INIS)

    Gills, T.E.; Gallorini, M.; Rook, H.L.

    1978-01-01

    Potentially toxic metals in the food chain that can lead to deleterious effects on human health have been well documented. Because of the toxicity of some metals, levels of 1 ppm or less must be routinely monitored in foods to ensure human safety. To ensure the accuracy of measurement, NBS in a cooperative interagency agreement with the Food and Drug Administration is involved in developing and certifying selected elements in food grain as a part of the Standard Reference Material program. Both instrumental and radiochemical neutron activation analysis were used to analyze two food grain standard reference materials (Rice and Wheat Flours) for trace element certification. (author)

  15. Determination of trace elements in standard reference materials by the ko-standardization method

    International Nuclear Information System (INIS)

    Smodis, B.; Jacimovic, R.; Stegnar, P.; Jovanovic, S.

    1990-01-01

    The k o -standardization method is suitable for routine multielement determinations by reactor neutron activation analysis (NAA). Investigation of NIST standard reference materials SRM 1571 Orchard Leaves, SRM 1572 Citrus leaves, and SRM 1573 Tomato Leaves showed the systematic error of 12 certified elements determined to be less than 8%. Thirty-four elements were determined in NIST proposed SRM 1515 Apple Leaves

  16. Determination of trace elements in Mesozoic dykes of the Serra do Mar by neutron activation

    International Nuclear Information System (INIS)

    Vicentini, Caio M.; Marques, Leila S.

    2013-01-01

    The analysis of trace elements such as rare earths, Th, U, Ta, Hf, Ba, Rb and Ba, is a very important tool for petrogenetic studies. In order to study these processes in dykes of Enxame Serra do Mar (Coast of Sao Paulo and Rio de Janeiro), belonging to the Parana Magmatic Province (PMP), one of the most significant provinces of continental basalts in the world, were perform analyzes by neutron activation in these dikes. The technique, employed in Centro de Reator de Pesquisa of the Instituto de Pesquisas Energeticas e Nucleares, provided concentrations of trace elements with accuracy levels of 10% and 9%, which are suitable for petrogenetic studies. Due to the low concentrations of the elements analyzed, the experimental routine sample preparation processes covered very careful to avoid contamination. The samples investigated can be divided into four groups: basic rocks (SiO 2 500; basic rocks with Ti / Y 2 2 > 63%). Dikes of intermediate and acid composition only occur at the Sao Sebastiao Island and adjacent coastal region. The concentrations of major and minor elements, as well as the abundance patterns of rare earths and other incompatible elements of these more differentiated rocks, show significant similarities with the type of the volcanic Chapeco, suggesting similar genesis, in other worlds, including also processes of crustal contamination

  17. Modified emission-transmission method for determining trace elements in solid samples using the XRF techniques

    International Nuclear Information System (INIS)

    Poblete, V.; Alvarez, M.; Hermosilla, M.

    2000-01-01

    This is a study of an analysis of trace elements in medium thick solid samples, by the modified transmission emission method, using the energy dispersion X-ray fluorescence technique (EDXRF). The effects of absorption and reinforcement are the main disadvantages of the EDXRF technique for the quantitative analysis of bigger elements and trace elements in solid samples. The implementation of this method and its application to a variety of samples was carried out using an infinitely thick multi-element white sample that calculates the correction factors by absorbing all the analytes in the sample. The discontinuities in the masic absorption coefficients versus energies association for each element, with medium thick and homogenous samples, are analyzed and corrected. A thorough analysis of the different theoretical and test variables are proven by using real samples, including certified material with known concentration. The simplicity of the calculation method and the results obtained show the method's major precision, with possibilities for the non-destructive routine analysis of different solid samples, using the EDXRF technique (author)

  18. Determination of trace elements in tailpipe fish produced in artificial farms and from white and blue nile

    International Nuclear Information System (INIS)

    Ahmed, Zeinb Khalil Elsaim

    2017-01-01

    In this study, an analytical protocol of x-ray fluorescence spectroscopy was used to determine the concentration of 13 trace elements, potassium (K), antimony (Sb), iron (Fe), copper (Cu), zinc (Zn), lead (Pb), bromine (Br), rubidium (Rb), strontium (Sr), mercury (Hg), chromium (Cu), manjense (Mn), and calcium (Ca), in tilapa fish. A total of 70 samples covering 35 fish samples collected from different states includes Eldamazine for blue nile samples and the Mawrada market for the white nile samples and 5 artificial fish farms samples were collected from Om badda in Omdurman and Bahry state for three farms Alsamraband Aldorshab and from Alshagra state in Khartoum, during may to June 2016. The trace elements detected in all samples, and the concentration in part million (ppm). The concentrations of trace elements followed the sequence of, K, Ca, Fe, Zn, Cu, Sr, Rb, Pb, but Cr, Hg and Ni were observed in one fish fram (farm A). The analysis included two tissues (flesh and gills), because most people in Sudan consume the flesh and gills, specially in the small fishes, consider as good indicators for the trace elements, and toxic compounds in general. The analysis indicated that the white nile fishes have higher l eves of most of the trace elements compared to the blue nile, e.g. Fe (560±186) in the white nile, whereas in the blue nile, (188±63). On the other hand , the artificial tilapia farms showed significant variations in the trace elements concentrations. The analysis revealed that a higher concentrations of most of the trace elements in gill tissues than flesh, e.g. Fe (1673±1453) in the flesh, and (9768±1175) in the gills. These results indicated that the gill accumulated higher levels of heavy metals than other organs, because they acted as a depot tissue. In addition, the post hoc test was performed following (Dunnett tests), using the blue nile group as a control group, since it has the lowest trace elements concentrations, among the river nile fishes in

  19. Internal standard method for determination of gallium and some trace elements in bauxite by neutron activation analysis

    International Nuclear Information System (INIS)

    Chen, S.G.; Tsai, H.T.

    1983-01-01

    A method is described for the determination of gallium and other trace elements such as Ce, Cr, Hf, Lu and Th in bauxite by the technique of neutron activation analysis using gold as internal standard. Isopropyl ether was used as organic extractant radioactive gallium from the sample. This method yields very good accuracy with a relative error of +-3%. (author)

  20. Determination of Trace and Volatile Element Abundance Systematics of Lunar Pyroclastic Glasses 74220 and 15426 Using LA-ICP-MS

    Science.gov (United States)

    McIntosh, E. Carrie; Porrachia, Magali; McCubbin, Francis M.; Day, James M. D.

    2017-01-01

    Since their recognition as pyroclastic glasses generated by volcanic fire fountaining on the Moon, 74220 and 15426 have garnered significant scientific interest. Early studies recognized that the glasses were particularly enriched in volatile elements on their surfaces. More recently, detailed analyses of the interiors of the glasses, as well as of melt inclusions within olivine grains associated with the 74220 glass beads, have determined high H2O, F, Cl and S contents. Such elevated volatile contents seem at odds with evidence from moderately volatile elements (MVE), such as Zn and K, for a volatile- depleted Moon. In this study, we present initial results from an analytical campaign to study trace element abundances within the pyroclastic glass beads. We report trace element data determined by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) for 15426 and 74220.

  1. Osteoporosis and trace elements

    DEFF Research Database (Denmark)

    Aaseth, J.; Boivin, G.; Andersen, Ole

    2012-01-01

    More than 200 million people are affected by osteoporosis worldwide, as estimated by 2 million annual hip fractures and other debilitating bone fractures (vertebrae compression and Colles' fractures). Osteoporosis is a multi-factorial disease with potential contributions from genetic, endocrine...... in new bone and results in a net gain in bone mass, but may be associated with a tissue of poor quality. Aluminum induces impairment of bone formation. Gallium and cadmium suppresses bone turnover. However, exact involvements of the trace elements in osteoporosis have not yet been fully clarified...

  2. World-wide intercomparison exercise for the determination of trace elements in Fucus sample IAEA-140. Report no. 64

    International Nuclear Information System (INIS)

    Coquery, M.; Carvalho, F.P.; Horvat, M.; Azemard, S.

    1997-09-01

    The accurate and precise determination of trace elements in marine samples is fundamental to pollution assessment in coastal and marine environments. Analyses of sea plants are important to investigate the uptake of toxic elements along the trophic chain and sea plants may be used as indicators for water pollution and to compare the levels of contamination of different aquatic environments. IAEA. together with UNEP and the Intergovernmental Oceanographic Commission (IOC) work closely with other producers of Reference Materials in order to assure a continuous supply of these vital compounds for quality assurance procedures. A full catalogue of materials is published regularly. The Marine Environmental Studies Laboratory (MESL) of IAEA-MEL has conducted intercomparison exercises on trace elements for over twenty years as part of its contribution to IAEA's Analytical Quality Control Service, UNEP's Regional Seas Programme. and, occasionally, in association with the IOC GIPME (Global Investigation of the Pollution in the Marine Environment) programme. This report describes the performance of laboratories in one intercomparison run conducted during 1996 that was organized for the determination of trace elements in a marine macro algae (Fucus sp.) sample. This study was intended to give laboratories responsible for trace element analyses of marine materials an opportunity for checking their analytical performance

  3. Determination of trace element concentration in infant head hair of Rawalpindi/Islamabad area using INAA technique

    International Nuclear Information System (INIS)

    Zaidi, J.H.; Gill, K.P.

    2004-01-01

    The concentration of 18 minor and trace elements (essential, toxic and nonessential) in infant head hair was determined. The data provide the base-line values of these elements in head hair of infants of low- and medium-income group subjects. The statistical results show that there are significant correlations between some elements such as: Ca-Zn, Ca-Fe, Mg-Ca, Mg-Mn and Mg-Fe. The results obtained have been compared with the data reported in the literature. Our data show compatibility of elemental contents of infant head hair with those from some of the other geological regions but also deviate in some cases. (orig.)

  4. Preconcentration of trace elements

    International Nuclear Information System (INIS)

    Zolotov, Yu. A.; Kuz'min, N.M.

    1990-01-01

    This monograph deals with the theory and practical applications of trace metals preconcentration. It gives general characteristics of the process and describes in detail the methods of preconcentration: solvent extraction, sorption, co-precipitation, volatilization, and others. Special attention is given to preconcentration in combination with subsequent determination methods. The use of preconcentration in analysis of environmental and biological samples, mineral raw materials, high purity substances, and various industrial materials is also considered

  5. Non-destructive determination of trace-element concentrations. Annual progress report, August 1979

    International Nuclear Information System (INIS)

    Gordon, G.E.; Zoller, W.H.; Walters, W.B.

    1979-08-01

    Development and testing of the neutron-capture prompt γ-ray activation analysis method continued. A wide range of NBS Standard Reference Materials, USGS Standard Rocks, and other materials have been analyzed in order to identify elements whose lines can be observed, to determine interferences and detection limits for each important γ ray of observable elements and to measure concentrations of observable elements for comparison with certified or other previous results. In most crustal samples, concentrations of 16 to 20 elements can be determined

  6. Essential trace elements content in a sudanese meal of cooked Hibiscus Sp. leaves as determined by both X-ray florescence and atomic absorption spectroscopy techniques

    International Nuclear Information System (INIS)

    Mohamed, S.M; Taha, M.H.

    2003-01-01

    Essential trace elements content of a Sudanese meal of cooked Karkadi plant leaves (Hibiscus Sp)was determined and found to be several folds higher than the average trace element content of Sudanese food as determined in twenty nine daily consumed mixed diets. Therefore, this plant can act as a promising natural supplement in cases of deficiency provided it is grown in a trace element rich soil. (Author)

  7. Simultaneous Determination of 30 Trace Elements in Cancerous and Noncancerous Human Tissue Samples with Gamma-ray Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Samsahl, K; Brune, D; Wester, P O

    1963-10-15

    The following trace elements were quantitatively determined by gamma-ray spectrometry in T samples of non-cancerous and 5 samples of cancerous human tissue: P, Ca, Cr, Fe, Co, Cu, Zn, As, Se, Br, Rb, Mo, Ag, Cd, Sb, Cs, La, Au, and Hg. In some of the samples the following elements were qualitatively determined: Ti+Sc, Ga, Sr, In, Ba, Ce, Hf, Os, Pt, and U. Most of the trace elements were found to be present in much higher concentrations in the non-cancerous than in the corresponding cancerous liver samples. In a typical run one sample each of cancerous and non-cancerous tissue was irradiated together with standards of the elements to be determined in a thermal flux of 2.10{sup 13} n/cm{sup 2}/sec. for 24 hours. The radioactive trace elements were separated into 16, and in some cases 18, groups by means of a chemical group separation method. Subsequently, the gamma spectrometric measurements were performed. Two persons can manage the chemical separations and measure the different activities from a run in 1,5 days. A new method of comparing unknown samples with standards was developed.

  8. Determination of some trace elements in edible crops grown in Jebel Merra area

    International Nuclear Information System (INIS)

    Mohamed, Abdelmoneim Adam

    2001-11-01

    This preliminary study was conducted in the area of Jebel Merra in South Darfour State, Western Sudan, With the aim of establishing a base-line data on trace element levels in foodstuffs cultivated in the region. 19 samples of vegetables, cereal grains, spices and fruits were collected from farms in Nyala, Derbat, Sunie and Gawa. With the exception of Nyala, the sampling farms were located on hill slopes using turus system as a means for water harvesting. Samples were analyzed for six trace elements, viz., Fe, Mn, Zn, Cu, Co and Cr using Atomic Absorption Spectroscopy (Aas). Comparison of the results with similar data from different parts of Sudan and from some other countries reveals that the foodstuffs grown in this high latitude region are relatively deficient in their elemental content. This salient feature conforms with well-known fact that, the soil in high latitude regions depleted in nutritional plant elements due to the leaching caused by runoff water hence the corresponding concentrations in plants are quite low indicative of state of malnutrition. Categorically speaking, among the vegetables analyzed, okra has shown a high affinity in accumulating Fe (187.49 ppm), Mn (80.31ppm), Cu (7.43 ppm) and Zn (12.74 ppm) comparative to other species. On the other hand, opposite trend was observed with sorghum as the poorest one with respect to its ability in concentrating Fe (55.57 ppm), Mn (4.19 ppm), Zn (5.25 ppm) and Cu (1.26 ppm) relative to millet, Wheat, Lupins and broad beans. With regard to spices covered in this investigation, garlic contains the lowest concentrations of all the elements analyzed and agree well with those found in onion the poorest of all the vegetables. Concentrations obtained were 108.78 ppm (Fe), 3.6 ppm (Mn), 4.6 ppm (Zn), 1.73 ppm (Cu) and 0.1 ppm (Cr) and 0.16 ppm (Co). On individual basis, the highest concentration of Mn was measured in lupins at 143.18 ppm. Cr content in all spices was found to be less than 1 ppm, whereas for Co

  9. Trace elements in sera of patients with hepatitis B: Determination and analysis

    Science.gov (United States)

    Saod, Wahran M.; Darwish, Nadiya T.; Zaidan, Tahseen A.; Alfalujie, Abdul Wahab A.

    2018-04-01

    Chronic Hepatitis B (HBV) is the leading cause of morbidity and mortality worldwide with about 248 million people having HBV infection. Trace elements e.g. copper (Cu), zinc (Zn), selenium (Se) and iron (Fe) are constituent components of many metal proteins and metalloenzymes in human sera. Therefore, the ratios of these trace elements in human sera are often stated to be a good marker for diagnosing various diseases including HBV. The aims of this study are: to compare the level of trace elements in sera of patients infected with HBV and healthy participants, and to evaluate the efficiency of analytical techniques (e.g. Inductively Coupled Plasma-Mass spectrometry (ICP-MS), Atomic Absorption Spectroscopy (hydride generation) (AAS) and Graphite Furnace Atomic Absorption Spectroscopy (GFAAS) that are currently used to detect Fe and Se elements in Patients' human sera. The findings of this study show that the concentration range of copper element between (132.80±28.64 µg/dl) to (105.66±23.20 µg/dl) was significantly higher in HBV infected patients as compared to those in healthy controls (91.27±9.20 µg/dl). Iron concentration range between (206.64±61.60 µg/l) to (170.00±36.71 µg/l) was significantly higher in HBV infected patients as compared to those in healthy controls (158.00±15.13 µg/l). However, patients with HBV had significantly lower serum concentrations of zinc with a concentration range between (111.64±20.90 µg/dl) to (99.25±24.06 µg/dl) as compared to those in healthy controls (113.44±16.38 µg/dl). While selenium concentration range between (64.39±7.39 µg/l) to (51.10±4.96 µg/l) was significantly lower in HBV infected patients as compared to those in healthy controls (67.68±7.60) (μg/l). Moreover, the results of this study suggest that (AAS) technique was the most accurate method to measure the concentration of selenium element, while (UV and ICP-MS) analytical techniques have the same efficiency in measuring the iron concentration.

  10. A Fast Radiochemical Method for the Determination of Some Essential Trace Elements in Biology and Medicine

    Energy Technology Data Exchange (ETDEWEB)

    Samsahl, K

    1966-02-15

    An anion-exchange method based on fast selective sorption steps from mixtures of sulfuric, hydrobromic, and hydrochloric acid solutions has been developed for the separation of five different groups of radioactive trace elements in neutron-irradiated biological material. The separations are performed automatically with a simple proportioning pump apparatus. The apparatus allows the exact adjustment of influent solutions to the series of ion-exchange columns. The practical application of the method is described in detail. The successful use of the method is practically independent on the level of Na activity present in the sample.

  11. Determination of trace elements in seawater by neutron activation analysis and electrochemical separation

    International Nuclear Information System (INIS)

    Jorstad, K.; Salbu, B.

    1980-01-01

    The combination of neutron activation analysis and electrolysis at a constant, controlled potential has proved itself to be a useful multielement method for the determination of 28 elements in seawater. After freeze-drying and irradiation, the samples are dissolved and electrolyzed for 1 h. The radioactive species deposited on the mercury cathode allow determination of 14 elements (Ag, As, Au, Cd, Co, Cr, Fe, Ga, Hg, La, Mo, Sb, Se, Zn). Another 14 elements (Ba, Br, Ca, Ce, Cs, Eu, Na, Rb, Sc, Sm, Sr, Th, U, Yb) are quantitatively determined by measuring the activities in the residual solution. To obtain a reproducible electrolysis, radioactive tracers have been used to study the decrease of element concentrations in solution as a function of time of electrolysis, the influence of the initial element concentration on the rate constant k, the effect of cathode material and of the pH in the solution. 4 figures, 4 tables

  12. Determination of trace elements in Katana (Japanese sword) by neutron activation analysis with multidimensional γ-ray spectrometry

    International Nuclear Information System (INIS)

    Okada, Y.; Hirai, S.; Ohya, S.; Kimura, Atsushi; Hatsukawa, Yuichi; Toh, Yosuke; Koizumi, Mitsuo; Oshima, Masumi

    2006-01-01

    In this study, we tried to measure trace elements (As and Sb) in Katana (Japanese swords) by multidimensional γ-ray spectrometry method (GEMINI-II) and conventional counting method for neutron activation analysis (NAA). The determined values by GEMINI-II and conventional counting were in good agreement with. Using the multidimensional γ-ray spectrometry (GEMINI-II) to determine As and Sb was improved by 7 times and 10 times compared with the conventional counting method. (author)

  13. Oesophageal cancer in the Transkei. Determination of trace element concentrations in selected plant material by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Renan, M.J.; Drennan, B.D.; Keddy, R.J.; Sellschop, J.P.F.

    1979-01-01

    The results of the analysis by instrumental neutron activation for the concentration of trace elements in plant materials from certain areas in the Transkei region of southern Africa are presented. These areas are selected for their characteristic high or low incidence of carcinoma of the oesophagus. To broaden the suite of elements for which analysed and to overcome some of the limitations of neutron activation analysis, certain other nuclear analyses and methods are suggested which, if utilized, would increase the number of elements determined, and so improve the information available. (author)

  14. Total reflection X-ray fluorescence as a convenient tool for determination of trace elements in microscale gasoline and diesel

    Science.gov (United States)

    Zhang, Airui; Jin, Axiang; Wang, Hai; Wang, Xiaokang; Zha, Pengfei; Wang, Meiling; Song, Xiaoping; Gao, Sitian

    2018-03-01

    Quantitative determination of trace elements like S, Fe, Cu, Mn and Pb in gasoline and S in diesel is of great importance due to the growing concerns over air pollution, human health and engine failure caused by utilization of gasoline and diesel with these harmful elements. A method of total reflection X-ray fluorescence (TXRF) was developed to measure these harmful trace elements in gasoline and diesel. A variety of factors to affect measurement results, including TXRF parameters, microwave-assisted digestion conditions and internal standard element and its addition, were examined to optimize these experimental procedures. The hydrophobic treatment of the surface of quartz reflectors to support the analyte with neutral silicone solutions could prepare thin films of gasoline and diesel digestion solutions for subsequent TXRF analysis. The proposed method shows good potential and reliability to determine the content of harmful trace elements in gasoline and diesel with high sensitivity and accuracy without drawing different standard calibration curves, and can be easily employed to screen gasoline and diesel in routine quality control and assurance.

  15. Trace elements in some new Romanian phytotherapeutic drugs determined by neutron activation analysis

    International Nuclear Information System (INIS)

    Preoteasa, E.A.; Salagean, M.; Pantelica, A.; Ionescu-Tirgoviste, C.

    1997-01-01

    Instrumental neutron activation analysis (INAA) has been performed on four new Romanian phytotherapeutic drugs registered us Fitolip, Fitodiab, Retinomion and Neuromion. The drugs were very well tolerated in clinical trials and are used in diabetes and other chronic diseases. They were prepared in the form of tablets made from dried powders of fruits, flowers, leaves and shells of plants used in non-conventional medicine. All four products are reach in various bioactive substances such as flavones, flavonoids, anthocyans, terpenes, rutosides, vitamins and essential fatty acids. Samples and multielemental reference materials were irradiated in a thermal neutron flux of 1.1 x 10 11 n.cm -2 .s -1 and measured with a high resolution Ge(Li) detector. 28 mineral elements were found, including Mg, K, Ca, Na and Fe at percent and sub-percent levels; Cl, Al and Mn between tens and thousands of ppm; Zn, Br, Rb and Ba up to tens of ppm; Cr, Cu, Co and V in the ppm range; and Sc, As, Sb, Cs, Lu, La, Ce, Sm, Hf, Au, Hg and Th up to hundreds of ppb. The intake of mineral elements provided by a cure of 3 pills/day shows the following: 1. None of the toxic elements As and Hg in the four drugs exceeds a noxious level; 2. Mg is the most abundant macro-element and a cure covers 15 - 60 % of the daily requirements; 3. Among essential microelements, Co may provide even more than 100% of the daily requirements; other elements may give small but significant fractions of the necessary daily amounts, e.g. 3-30% for Cr, 5-20% for Mn, and 2-10% for Fe; 4. The supply of Al, the most abundant unessential metal represents 6 - 40 % of the known daily intake. Thus a 3 pills/day cure could contribute positively to the therapy of various diseases by providing Mg, Mn, Cr (a trace element deficient in diabetes), Fe and Co, but higher daily doses could result in a Co oversupply. Further in INAA studies on biological examples from patients taking these new medicines are needed to understand the

  16. The determination of low level trace elements in coals by laser ablation-inductively coupled plasma-mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Booth, C.A.; Spears, D.A.; Krause, P.; Cox, A.G. [University of Sheffield, Sheffield (United Kingdom). Dept. of Earth Sciences

    1999-11-01

    The rapid determination of elements present in low level concentrations in bituminous coals is possible using laser abalation-inductively coupled plasma-mass spectrometry (l.a.-i.c.p.-m.s.). A wide range of trace elements can routinely be determined using this technique but it is for environmentally sensitive elements, such as As, Cd, Mo, Sb, Se and Hg, that it is of most use due to the low levels of detection. Calibration of the i.c.p.-m.s. was achieved using a series of uncertified coals and the method evaluated using the South African certified coals, Sarm 18, 19 and 20. A critical evaluation of the data obtained shows that for many of the elements studied the results obtained are both accurate and precise, even at very low concentrations, with the limits of detection for all of the elements being in the {mu}g/kg (parts per billion) range. 6 refs., 3 figs., 9 tabs.

  17. Determination of some trace elements in Elsaraf Dam area using AAS and XRF

    International Nuclear Information System (INIS)

    Yagob, T. I.; Ahmed, T. E. A.

    2006-12-01

    To screen the plants in Elsaraf dam (Gedaref-Sudan), for their ability to uptake metal ions and the effect of seasonal rain on the availability of these metal ions for plants, trace elements in plant roots and the associated soil were studied in two seasons using atomic absorption spectroscopy and x-ray fluorescence. The nutrient elements, (Fe, Mn, Zn, Cu, Co) showed higher concentrations than toxic elements (Cr, Ni, Cd) in both plant and soil samples. Iron has the highest concentration 549/5660 and 3358/3680 mg/100 g, manganese has shown the second highest concentration followed by nickel and zinc. Copper, cobalt and chromium have shown relatively similar concentrations,while cadmium has the lowest concentration. In general, almost for all elements the soils have shown higher concentration followed by the plant. Estimation of soil/plant transfer factor (CR) that Cyperus rotandus has the highest affinity toward accumulating most of the metal ions, while the rest of plants have shown almost almost similar affinity.(Author)

  18. Trace elements in several species of crustaceans of Amami Island Group in Japan determined by activation analysis

    International Nuclear Information System (INIS)

    Fukushima, M.; Tamate, H.; Nakano, Y.

    2001-01-01

    Concentration levels of trace elements were determined in several species of subtropical crustaceans from Amami Islands in Japan in order to evaluate the levels of specific accumulation of elements among species. Tissue samples prepared from gill, muscle, hepatopancreas, and testis were irradiated for photon activation analysis (PAA) and neutron activation analysis (NAA). By PAA and NAA, eighteen elements could be determined. The levels of Br and I were extremely high in gills of spiny lobster and shovel-nosed lobster, respectively. A high concentration of Ag was found in the hepatopancreas of spiny lobsters collected from the Amami Island, while this element was not detected in the same species collected from Toba. The results suggest that the distribution of the trace elements in different tissues and species varies according to both species and environmental differences. To study the molecular forms of the elements in tissue, fractions that contained protein-bound elements from the hepatopancreas of spiny lobsters were separated by ultracentrifugation and gel filtration chromatography. Elution profiles of the chromatography suggest that Cu, Fe, and Se were bound to proteins, while Ag was not. (author)

  19. Ecological and biological determinants of trace elements accumulation in liver and kidney of Pontoporia blainvillei

    Energy Technology Data Exchange (ETDEWEB)

    Seixas, Tercia G. [Departamento de Quimica, PUC-Rio, 22453-900 Rio de Janeiro, RJ (Brazil); Laboratorio de Radioisotopos Eduardo Penna Franca, IBCCF-UFRJ, 21941-902 Rio de Janeiro, RJ (Brazil)], E-mail: tercia@rdc.puc-rio.br; Kehrig, Helena do A. [Laboratorio de Radioisotopos Eduardo Penna Franca, IBCCF-UFRJ, 21941-902 Rio de Janeiro, RJ (Brazil); Fillmann, Gilberto [Departamento de Oceanografia, FURG, 96201-900 Rio Grande, RS (Brazil); Di Beneditto, Ana Paula M.; Souza, Cristina M.M. [Laboratorio de Ciencias Ambientais, CBB-UENF, 28013-602 Campos dos Goytacazes, RJ (Brazil); Secchi, Eduardo R. [Departamento de Oceanografia, FURG, 96201-900 Rio Grande, RS (Brazil); Laboratorio de Tartarugas e Mamiferos Marinhos, Departamento de Oceonagrafia e Museu Oceanografico ' Prof. E.C. Rios' , FURG, 96201-900, Rio Grande, RS (Brazil); Moreira, Isabel [Departamento de Quimica, PUC-Rio, 22453-900 Rio de Janeiro, RJ (Brazil); Malm, Olaf [Laboratorio de Radioisotopos Eduardo Penna Franca, IBCCF-UFRJ, 21941-902 Rio de Janeiro, RJ (Brazil)

    2007-10-15

    The present work tested whether ecological and biological variables have an influence on the assimilation of trace elements by the tissues of a cetacean from the Western South Atlantic Ocean. No significant differences were observed in the concentrations for both sexes. As individuals from the two sampling areas belong to distinct genetic and morphological populations, animals of similar body length were older on the southeastern than on the southern coast. The liver showed the highest concentrations of mercury, whereas the highest levels of cadmium were found in the kidney. Hepatic mercury, cadmium and selenium in individuals from the south coast were about four times as high as those from the southeast coast. However, arsenic in the liver and kidney were similar in both coastal areas. Hepatic mercury, cadmium and selenium concentrations increased with body length in individuals from the southeastern coast, although no significant correlations (P > 0.05) were observed between body length from either area and the renal and hepatic As concentrations. A significant positive linear relationship was observed between molar concentrations of Hg and Se in the liver of all individuals from both areas (r{sup 2} = 0.93; P < 0.001), presenting Se:Hg ratios close to 4. Differences found among the concentrations of Hg, Cd and Se in dolphins from both areas were probably due to the preferred prey, bioavailability of elements in each marine environment, and environment variables (water temperature, net primary production). As a consequence, concentrations of trace elements in the tissues of this species can be considered to be a result of the surrounding environment.

  20. Determination of trace elements in fresh cow's milk in Khartoum state

    International Nuclear Information System (INIS)

    Mohammed, Elamin Mohammed Abd Allah

    2017-01-01

    Milk and its products are basic foodstuffs and constitute and important source of some vitamins and a lot of minerals. However, increasing or decreasing intake of theses minerals can be harmful. The aim of this study is to measure the concentrations of macro and trace elements in fresh cow's milk namely, Cl, K, Ca, Cr, Mn, Fe, Ni, Cu, Zn, Pb, Br, Rb and Sr. A total of 40 samples of fresh cow's milk were collected from different dairy farms located around farms located around Khartoum state, 20 of them collected from cows drink ground water, while the other 20 samples their cows drink river water. Samples were then dried by freeze drying, and analyzed by energy dispersive x-ray fluorescence system. A certified reference sample, obtained from International Atomic Energy Agency was used for quality control analysis, to ensure the reliability of the device. The results obtained were expressed as (mean±uncertainty). The obtained results revealed that some elements i, e, Cl, K, Ca showed clear variation in the levels of their concentrations, compared to the relevant previous studies, which sometime found to be higher and lower than the reported values. While the trace element such as Cr, Mn, Fe, Ni, Cu, Zn, Pb, Br showed higher levels. It was observed that the milk samples of cows drink ground water had significantly higher concentration of Marco elements (Cl, K, Ca) than the milk of cows drink river water (at probability level of p-value<0.05). The elements concentration in the milk of cows drink ground water had also higher concentration of Cu and Br, and lower concentration of Fe, Zn, Pb, Rb and Sr than the milk of cows drink river water. However it is not statistically significant. Some elements such as: Cr, Mn and Ni present in high concentration in the milk of cows drink ground water, while they were not detected in the milk of cows drink river water. The statistical test one way analysis of variance (ANOVA) (at probability level of p-value<0.05) showed

  1. Trace elements in human pituitary

    International Nuclear Information System (INIS)

    Kanabrocki, E.L.; Greco, J.; Graham, L.A.; Kaplan, E.; Rubnitz, M.E.; Oester, Y.T.; Brar, S.; Gustafson, P.S.; Nelson, D.M.; Molinari, F.; Moore, C.E.; Kanabrocki, J.A.

    1976-01-01

    Neutron activation analysis was used to determine several trace elements in human pituitaries from adult subjects aged 42 to 83 years who had died of ischemic heart disease, carcinoma and cirrhosis of the liver. None of these subjects suffered from mental disease. The concentrations of Fe, Zn, Rb, Se, Br, Cr, Hg, Cs and Co in dried tissue showed no correlation with the diseases, and the results may therefore be representative of the general population. These elements may play a very fundamental role in pituitary function. (U.K.)

  2. DETERMINATION of the TRACE ELEMENT LEVELS in HAIR of SMOKERS and NON-SMOKERS by ICP-MS

    Directory of Open Access Journals (Sweden)

    Elif Varhan Oral

    2016-09-01

    Full Text Available For at least 50 years, determination of the trace element levels in human hair has been used to assess environmental and vocational exposure to toxic elements . As compared to other biological matrices (e.g. blood, urine, human hair is stable and therefore useful as a matrice. In this study, analyses of toxic and essential trace elements, such as Cd, Pb, Cu and Fe, were done in hair samples which we collected from male smokers (10 people and non-smokers (10 people who live in Diyarbakır, Turkey and concentrations in hair samples were compared. Hair samples were washed by a standard procedure proposed by the International Atomic Energy Agency. Then the samples were dried for 16 h at 110°C in an oven. Solubilization procedure was carried out by nitric acid hydrogen peroxide mixture (3:1 in closed vessels in a microwave oven. Trace element analyses were carried out by using inductively coupled plasma-mass spectrometry (ICP-MS  technique. In our study, while concentrations of Cd, Pb, and Fe elements were found to be considerably higher in smokers than non-smokers, similar results were observed in Cu concentrations. The precision and accuracy of the method was evaluated by applying spike method to samples. Analytical recovery results were found between 91.2% and 104.6%.

  3. XRF and TXRF techniques for multi-element determination of trace elements in whole blood and human hair samples

    International Nuclear Information System (INIS)

    Khuder, A.; Karjou, J.; Sawan, M.Kh.; Bakir, M.A.

    2007-01-01

    XRF and TXRF were established as useful techniques for multi-element analysis of whole blood and human head hair samples. Direct-XRF with different collimation units and different X-ray excitation modes was successfully used for the determination of S, P, K, Ca, Fe, and Br elements in blood samples and K, Ca, Mn, Fe elements in human hair samples. Direct analysis by TXRF was used for the determination of Rb and Sr in digested blood and human hair samples, respectively, while, the co-precipitation method using APDC for TXRF analysis was used for the determination of Ni, Cu, Zn, and Pb elements in both matrices. As a result, the improved XRF and TXRF methods were applied for multi-element determination of elements in whole blood and human hair samples in non-occupational exposed population living in Damascus city. The mean concentrations of analyzed elements in both matrices were on the reported range values for non-occupational population in other countries. (author)

  4. XRF and TXRF techniques for multi-element determination of trace elements in whole blood and human hair samples

    International Nuclear Information System (INIS)

    Khuder, A.; Karjou, J.; Sawan, M.Kh.; Bakir, M.A.

    2008-01-01

    XRF and TXRF were established as useful techniques for multi-element analysis of whole blood and human head hair samples. Direct-XRF with different collimation units and different X-ray excitation modes was successfully used for the determination of S, P, K, Ca, Fe, and Br elements in blood samples and K, Ca, Mn, Fe elements in human hair samples. Direct analysis by TXRF was used for the determination of Rb and Sr in digested blood and human hair samples, respectively, while, the co-precipitation method using APDC for TXRF analysis was used for the determination of Ni, Cu, Zn, and Pb elements in both matrices. As a result, the improved XRF and TXRF methods were applied for multi-element determination of elements in whole blood and human hair samples in non-occupational exposed population living in Damascus city. The mean concentrations of analyzed elements in both matrices were on the reported range values for non-occupational population in other countries. (author)

  5. Trace elements determination in red and white wines using total-reflection X-ray fluorescence

    International Nuclear Information System (INIS)

    Anjos, M.J.; Lopes, R.T.; Jesus, E.F.O. de; Moreira, S.; Barroso, R.C.; Castro, C.R.F.

    2003-01-01

    Several wines produced in different regions from south of Brazil and available in markets in Rio de Janeiro were analyzed for their contents of elements such as: P, S, Cl, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Rb and Sr. Multi-element analysis was possible with simple sample preparation and subsequent analysis by total-reflection X-ray fluorescence using synchrotron radiation. The measurement was carried at the X-ray fluorescence beamline in the Synchrotron Light Source Laboratory in Campinas, Brazil. The levels of the various elements obtained were lower in the Brazilian wines than the values generally found in the literature. The present study indicates the capability of multi-element analysis for determining the contents of various elements present in wines coming from Brazil vineyards by using a simple, sensitive and precise method

  6. Methodology for determination of trace elements in mineral phases of iron banded formation by LA-ICP-MS

    International Nuclear Information System (INIS)

    Sousa, Denise V.M. de; Nalini Junior, Herminio A.; Sampaio, Geraldo M.S.; Abreu, Adriana T. de; Lana, Cristiano de C.

    2015-01-01

    The study of the chemical composition of mineral phases of iron formation (FF), especially of trace elements, is an important tool in the understanding of the genesis of these rocks and the contribution of the phases in the composition of whole rock. Low mass fraction of such elements in the mineral phases present in this rock type requires a suitable analytical procedure. The laser ablation technique coupled with ICP-MS (LA-ICP-MS) has been widely used for determination of trace elements in geological samples. Thus, the aim of this study is to develop calibration curves for determination of trace elements (Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) in mineral phases of banded iron formations by LA-ICP-MS. Several certified reference materials (CRM) were used for calibrate the equipment. The analytical conditions were checked by CRM NIST SRM 614. The results were satisfactory, since the curves showed good linearity coefficients, good accuracy and precision of results. (author)

  7. Report on the intercomparison runs for the determination of trace and minor elements in cabbage material. IAEA-359

    International Nuclear Information System (INIS)

    Campbell, M.J.; Radecki, Z.; Trinkl, A.; Burns, K.I.

    2000-04-01

    In 1989, the IAEA decided to produce a cabbage plant reference material that could be characterised for certain agrochemical residues. The cabbage plants (Brassica oleracea var. Sabauda) were grown from seed in Seibersdorf, Austria. The plants were treated with ten different agrochemical products during their growing period. Subsequently, it was decided that the material would also be valuable as a reference material for trace element analysis and quality control purposes. The property values for the trace metal content of the cabbage material, designated IAEA 359, were to be ascribed on the basis of information received from international intercomparison exercises. In parallel, it was decided to despatch the material as part of a joint IAEA-NIST (National Institute of Standards and Technology, USA) project to certify the trace and minor element contents of a spinach reference material (NIST 1570a), in which it was to serve as a quality control material. A similar rationale was used to justify inclusion of IAEA 359 in a small scale exercise for a preliminary characterisation of another IAEA reference material, IAEA 336 Lichen. Between 1992 and 1993, the material was used in 4 projects (2 large scale and 2 smaller scale) where its trace element contents were determined. This report deals with the statistical evaluation of the pooled analytical data from these exercises

  8. Trace element analysis of soy sauce

    International Nuclear Information System (INIS)

    Tomita, Michio; Haruyama, Yoichi; Saito, Manabu

    1994-01-01

    Trace elements in soy sauce have been measured by means of in-air PIXE. Six kinds of trace elements were detected, such as Mu, Fe, Ni, Zn, Cu and Br. Concentrations of Mn, Fe, Zn and Br which were observed in all samples, have been determined. Each analyzed sample contained considerable amount of bromine about 160 ppm. (author)

  9. Trace elements determination in ginseng and ginkgo biloba medicinal plants; Determinacao de elementos traco nos fitofarmacos ginseng e ginkgo biloba

    Energy Technology Data Exchange (ETDEWEB)

    Avino, Simone; Saiki, Mitiko; Fulfaro, Roberto [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil). Lab. de Analise por Ativacao Neutronica

    2002-07-01

    Determinations of trace elements in medicinal plants or in their extracts are of great interest since some elements are components of active constituents or they can affect the plant metabolism and consequently the formation of active constituents. In this work, inorganic components in medicinal drugs, Ginseng e Ginkgo Biloba provided from different laboratories, were analyzed by neutron activation analysis. Elements As, Br, Ca, Cl, Co Cr, Cs, Fe, K, La, Mg, Mn, Na, Rb, Sb, Sc, and Zn, were determined in these samples. Comparisons carried out between the results obtained for samples from different laboratories indicated distinct concentrations for several elements. These results may be attributed to the effect of soil composition and environmental conditions where these plants were cultivated. The precision and accuracy of the results were evaluated by analyzing reference materials Bowen's Kale from IUAPC and Cabbage from IAEA. (author)

  10. Trace element determination using static high-sensitivity inductively coupled plasma optical emission spectrometry (SHIP-OES).

    Science.gov (United States)

    Engelhard, Carsten; Scheffer, Andy; Nowak, Sascha; Vielhaber, Torsten; Buscher, Wolfgang

    2007-02-05

    A low-flow air-cooled inductively coupled plasma (ICP) design for optical emission spectrometry (OES) with axial plasma viewing is described and an evaluation of its analytical capabilities in trace element determinations is presented. Main advantage is a total argon consumption of 0.6 L min(-1) in contrast to 15 L min(-1) using conventional ICP sources. The torch was evaluated in trace element determinations and studied in direct comparison with a conventional torch under the same conditions with the same OES system, ultrasonic nebulization (USN) and single-element optimization. A variety of parameters (x-y-position of the torch, rf power, external air cooling, gas flow rates and USN operation parameters) was optimized to achieve limits of detection (LOD) which are competitive to those of a conventional plasma source. Ionic to atomic line intensity ratios for magnesium were studied at different radio frequency (rf) power conditions and different sample carrier gas flows to characterize the robustness of the excitation source. A linear dynamic range of three to five orders of magnitude was determined under compromise conditions in multi-element mode. The accuracy of the system was investigated by the determination of Co, Cr, Mn, Zn in two certified reference materials (CRM): CRM 075c (Copper with added impurities), and CRM 281 (Trace elements in rye grass). With standard addition values of 2.44+/-0.04 and 3.19+/-0.21 microg g(-1) for Co and Mn in the CRM 075c and 2.32+/-0.09, 81.8+/-0.4, 32.2+/-3.9 for Cr, Mn and Zn, respectively, were determined in the samples and found to be in good agreement with the reported values; recovery rates in the 98-108% range were obtained. No influence on the analysis by the matrix load in the sample was observed.

  11. Determination of trace elements in lichen samples by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Saiki, Mitiko; Horimoto, Lidia K.; Vasconcellos, Marina B.A.; Marcelli, Marcelo P.; Sumita, Nairo M.; Saldiva, Paulo H.N.

    2001-01-01

    Samples of Canoparmelia texana lichen collected in different sites of Sao Paulo and Parana States, Brazil, were analysed by neutron activation analysis in order to obtain preliminary information on the air quality in these regions and also to select a region of interest for biomonitoring studies. Also Tadescantia pallida plant has been analysed in order to study the viability of using this specimen in environmental pollution monitoring. Lichens samples were collected from tree barks which were also collected to investigate the contribution of substrate derived elements to elements present in lichens. Young and old leaves of T. pallida were collected separately in order to study the leaf age effects on their elemental levels. The samples were cleaned, washed with distilled water, dried and ground for the analyses. Samples and standards were irradiated at the IEA-Rlm nuclear reactor for short and long periods and concentrations of the elements Al, As, Ca, Cd, Cl, Co, Cr, Cs, Fe, Hf, Mg, Mn, Rb, Sb, Sc, D, Th, U, V Zn and lanthanides were determined. Preliminary results obtained for T. texana lichen indicated that three sites (Ibiuna, Botanical Garden and Parque de Vila Velha) present low concentrations of the most elements analysed. Therefore lichens from these regions could be analysed to establish baseline levels of elements for monitoring purposes. Samples collected in open areas presented high concentrations of some elements probably due to the accumulation of elements originating from soil and from heavy vehicular traffic. Elemental concentrations obtained in outer barks were similar or smaller than those results obtained for lichens. Results obtained for T. pallida indicated that concentrations of elements in old leaves of this plant are of the same magnitude or slightly higher than those presented in young ones. (author)

  12. Determination of trace elements in Ethiopian, Vietnamese, and Japanese women using high-resolution IC-PMS.

    Science.gov (United States)

    Tekeste, Zinaye; Amare, Bemnet; Asfaw, Fanaye; Fantahun, Bereket; van Nguyen, Nhien; Nishikawa, Takeshi; Yabutani, Tomoki; Okayasu, Takako; Ota, Fusao; Kassu, Afework

    2015-10-01

    Humans and other living organisms require small quantities of trace elements throughout life. Both insufficient and excessive intakes of trace elements can have negative consequences. However, there is little information on serum level of trace elements in different populations. This study examines serum levels of trace elements in Ethiopian, Japanese, and Vietnamese women. Random samples of healthy women who were referred for routine hospital laboratory examinations in the cities of Hanoi, Sapporo, and Gondar were invited to participate in the study. Serum levels of magnesium, zinc, copper, iron, selenium, and calcium were determined using an inductively coupled plasma mass spectrometer. Furthermore, body mass index of each study participant was determined. The mean ± SD serum concentrations of zinc (μg/dL), copper (μg/dL), iron (μg/dL), selenium (μg/dL) and calcium (mg/dL), respectively, were 76.51 ± 39.16, 152.20 ± 55.37, 385.68 ± 217.95, 9.15 ± 4.21, and 14.18 ± 3.91 in Ethiopian women; 111.49 ± 52.92, 105.86 ± 26.02, 155.09 ± 94.83, 14.11 ± 3.41, and 11.66 ± 2.51 in Vietnamese women; and 60.69 ± 9.76, 107 ± 156, 268 ± 128, 8.33 ± 3.65, and 11.18 ± 0.68 in Japanese participants. Ethiopian women had significantly higher level of serum calcium than Vietnamese and Japanese women (both P Vietnamese women was higher than in women from Japan, the difference was not statistically significant (P > 0.05). Furthermore, compared with Japanese women, Ethiopian women had significantly high iron and copper concentrations (P Vietnamese than Ethiopian women. The study revealed a remarkable difference in serum concentrations of trace elements in women from different countries, implying differences in trace elements in the food or soil. Copyright © 2015 Elsevier Inc. All rights reserved.

  13. Brain trace elements and aging

    International Nuclear Information System (INIS)

    Hebbrecht, Geert; Maenhaut, Willy; Reuck, Jacques de

    1999-01-01

    Degenerative mechanisms involved in the aging process of the brain are to a certain extent counteracted by repair mechanisms. In both degenerative and recovery processes, trace elements are involved. The present study focused on the role of two minor (i.e., K and Ca) and six trace elements (i.e., Mn, Fe, Cu, Zn, Se and Rb) in the aging process. The elements were determined by PIXE in cerebral cortex and white matter, basal ganglia, brainstem and cerebellar cortex of 18 postmortem human brains, from persons without a history of neurologic or psychiatric disease who deceased between the age of 7 and 79. This age range allowed us to study the relationship between elemental concentrations and age. The most prominent findings were a concentration decrease for K and Rb and a concentration increase for the elements Ca, Fe, Zn and Se. The study supports recent findings that Ca and Fe are involved in brain degenerative processes initiated by oxygen free radicals, whereas Zn and Se are involved in immunological reactions counteracting the aging process

  14. Experiments made to separate the trace elements in seawater by extraction and their determination by neutron activation analysis

    International Nuclear Information System (INIS)

    Heuss, E.; Lieser, K.H.

    1979-01-01

    The problems of trace element determination in seawater by neutron activation analysis are discussed. Experiments with tri-n-octylphosphinoxide (TOPO) did not bring satisfactory results because of the strong interference of the bremsstrahlung from 32 P. Experiments with oxin at different pH showed that in each case only few elements are extracted in greater amounts. An extraction apparatus is described making possible the extraction of up to 10 l water by 50 ml of an organic solution. Extraction experiments using different complexing agents were satisfactory but the evaporation of the organic phase to dryness for irradiation was difficult. (author)

  15. Stratospheric particles: Synchrotron x-ray fluorescence determination of trace element contents

    International Nuclear Information System (INIS)

    Sutton, S.R.; Flynn, G.J.

    1987-01-01

    The first trace element analyses on stratospheric particles using synchrotron x-ray fluorescence (SXRF) are reported. Cr, Mn, Fe, Ni, Cu, Zn, Ga, Ge, Se and Br were detected. Concentrations for chondritic particle U2022G1 are within a factor of 1.7 of CI for all elements detected with the exception of Br which is 37 times CI. Chondritic particle W7029*A27 is also near CI for Cr, Mn, Fe, Ni, Cu, Zn and Ge but enriched in Ga, Se, and Br by factors of 5.8, 3.5 and 8.4, respectively. The third particle of the cosmic dust class also showed high Br enriched relative to CI by a factor of 28. Br was also detected at a high level in an aluminum-rich particle classified as probable artificial terrestrial contamination but exhibiting a chondritic Fe/Ni ratio. Br was not detected in a fifth particle also classified terrestrial and exhibiting a crustal Fe/Ni ratio. If the high Br has a pre-terrestrial origin, the ubiquity of the effect suggests that a large fraction of the chondritic interplanetary dust particles derive from a parent body (bodies) not sampled in the meteorite collection. 26 refs., 3 figs., 3 tabs

  16. [Standard sample preparation method for quick determination of trace elements in plastic].

    Science.gov (United States)

    Yao, Wen-Qing; Zong, Rui-Long; Zhu, Yong-Fa

    2011-08-01

    Reference sample was prepared by masterbatch method, containing heavy metals with known concentration of electronic information products (plastic), the repeatability and precision were determined, and reference sample preparation procedures were established. X-Ray fluorescence spectroscopy (XRF) analysis method was used to determine the repeatability and uncertainty in the analysis of the sample of heavy metals and bromine element. The working curve and the metrical methods for the reference sample were carried out. The results showed that the use of the method in the 200-2000 mg x kg(-1) concentration range for Hg, Pb, Cr and Br elements, and in the 20-200 mg x kg(-1) range for Cd elements, exhibited a very good linear relationship, and the repeatability of analysis methods for six times is good. In testing the circuit board ICB288G and ICB288 from the Mitsubishi Heavy Industry Company, results agreed with the recommended values.

  17. Analytic determination of the activation of essential and toxic trace elements in biological material

    International Nuclear Information System (INIS)

    Schelenz, R.

    1980-01-01

    A neutron activation-analysis technique for the multielement determination in biological material was developed. The individual steps of this procedure comprise radiochemical and also instrumental analytic techniques. After radiochemical separation 34 elements can be determined, after only instrumental procedures 26 elements can be detected in biological material. The radiochemical analysis of 34 elements lasts 4 days. Tracer investigations on the radionuclide retention of the anorganic separators HAP, TiP and ZP in 9N aqueous HNO 3 solution indicated that apart from Na-24, K-42 and P-32 the radionuclides Cs-134, Rb-86 and Se-75 are almost quantitatively adsorbed at the separators. For the remaining investigated radionuclides different but well-reproducible retention values resulted. The pH-value only slightly influences the extent of the radionuclide retention. Kinetic investigations on the radiochemical precipitation of some radionuclides on Cu and Cu(Hg)sub(x) were carried out. The depositing of the radionuclides Ag-110m, Hg-203 and Se-75 at 0 0 C and room temperature on Cu(Hg)sub(x) and Cu foil is a first order reaction. The half-life periods and the velocity constants of the depositing on Cu and Cu(Hg)sub(x) were determined for the investigated radionuclides in dependency of the temperature. The technique was examined by means of international biological multielement standards of known element combinations. The realisation of ring tests for the multielement determination in potatoe and milk powder showed that this method provides precise results. The applicability of the radiochemical method was confirmed by the simultaneous determination of 25 elements in overall nutrition samples. The instrumental technique was applied for the multielement determination in human hair (of the head) and in river water. (orig./MG) [de

  18. Trace element determination in plant material by means of instrumental neutron activation analysis (INAA) with special reference to molybdenum

    International Nuclear Information System (INIS)

    Schnier, C.; Schnug, E.

    1981-01-01

    The instrumental neutron activation analysis (INAA) permits a non-destructive multielement determination of minute trace element concentrations in organic material. No sample preparation except drying is required. Especially for the determination of molybdenum the INAA offers great advantages compared to the methods used in agricultural chemistry where complicated enrichment and extraction steps are needed. Contamination by reagents or loss of elements are not potential sources of errors. The principle, the advantages and disadvantages of INAA are described. The method is demonstrated with the example of celery samples from an experiment with five different nitrogen fertilizers on contaminated soil and of cabbage samples from an uncontaminated region. Besides molybdenum, 19 other elements (Na, K, Ca, Sc, Cr, Fe, Co, Zn, As, Se, Br, Rb, Cd, Sb, Ba, La, W, Au, Th) are determined. (orig.) [de

  19. Microwave assisted digestion of atmospheric aerosol samples followed by inductively coupled plasma mass spectrometry determination of trace elements

    Energy Technology Data Exchange (ETDEWEB)

    Swami, K.; Judd, C.D.; Orsini, J.; Yang, K.X. [New York State Dept. of Health, Albany, NY (United States). Wadsworth Center for Labs. and Research; Husain, L. [New York State Dept. of Health, Albany, NY (United States). Wadsworth Center for Labs. and Research; Dept. of Environmental Health and Toxicology, State Univ. of New York, Albany (United States)

    2001-01-01

    A microwave digestion method in a closed vessel was developed for the determination of trace metals in atmospheric aerosols using inductively coupled plasma mass spectrometry (ICP-MS). A recovery study for the elements V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Cd, Sb, and Pb was conducted using multi-elemental standard solutions, NIST 1633b Trace Elements in Coal Fly Ash, and NIST 1648 Urban Particulate Matter. A simple digestion method using only HNO{sub 3}/H{sub 2}O{sub 2}gave good recoveries (90%-108%) for all elements except Cr in SRM 1648, but yielded low recoveries for SRM 1633b. A more robust method using HNO {sub 3}/H {sub 2}O {sub 2}/HF/H {sub 3}BO {sub 3} yielded higher recoveries (82%-103%) for the lighter elements (V - Zn) in SRM 1633b, and improved the Cr recovery in SRM 1648, but decreased the Se recovery in both SRMs. A comparative analysis of aerosol samples obtained at a remote mountain location Nathiagali, Pakistan (2.5 km above mean sea level), and Mayville, New York, downwind from the highly industrialized Midwestern United States, was carried out using Instrumental Neutron Activation Analysis (INAA) for the elements Cr, Mn, Fe, Co, Zn, As, Se, and Sb. The simple digestion method yielded excellent agreement for Cr, Fe, Zn, As, Se, and Sb, with slopes of the ICP-MS vs. INAA regressions of 0.90-1.00 and R {sup 2} values of 0.96-1.00. The regressions for Mn and Co had slopes of 0.82 and 0.84 with R {sup 2} values of 0.83 and 0.82, respectively. Addition of HF/H {sub 3}BO {sub 3} did not improve the correlation for any of the elements and degraded the precision somewhat. The technique provides sensitivity and accuracy for trace elements in relatively small aerosol samples used in atmospheric chemistry studies related to SO {sub 2} oxidation in cloud droplets. The ability to determine concentrations of a very large number of elements from a single analysis will permit source apportionment of various trace pollutants and hence strategies to control the

  20. Provenance determination of pottery by trace element analysis. Problems, solutions and applications

    International Nuclear Information System (INIS)

    Mommsen, H.

    2001-01-01

    Provenance determinations of pottery by chemical analysis is reviewed and shown to work well. Since pottery is produced from a well homogenized clay paste according to a certain recipe, sharp elemental patterns are expected for a series of products having the same origin. To obtain such patterns when forming compositional groups of pottery, a consideration of experimental errors, a correction for dilution and a choice of only stable elements is necessary. The patterns thus obtained will have low probability of overlap with groups of different origin. Examples for well defined groups of German stonewares and of Mycenaean wares from the Peloponnese are recorded. (author)

  1. The IAEA worldwide intercomparison exercises (1990-1997). Determination of trace elements in marine sediments and biological samples

    International Nuclear Information System (INIS)

    Coquery, M.; Carvalho, F.P.; Azemard, S.; Horvat, M.

    1999-01-01

    Four major worldwide intercomparison exercises for the determination of trace elements in various environmental matrices were completed by the IAEA Marine Environment Laboratory since 1990: SD-M-2/TM, deep sea marine sediment; IAEA-350, tuna fish homogenate; IAEA-356, contaminated coastal sediment and IAEA-140, sea plant (Fucus sp.). These intercomparison exercises aim at enabling individual laboratories to monitor their performance. The results of these exercises allowed us to make an overall evaluation of the quality of data provided for environmental assessment and to identify the trends of analytical performance in the determination of trace elements over the years. The number of participants in each exercise varied between 68 and 130, and permits statistical evaluation of the performance for a number of elements. For each intercomparison exercise, the performance of the participant laboratories was assessed by comparing reported results with established reference values calculating 'Z-scores'. The results show that for each sample matrix, the values reported by some laboratories were far from satisfactory in the earlier exercises, in particular for Cd, Cr and Pb. Nevertheless, over time, a general improvement of performance can clearly be seen for all elements. Moreover, there was a noticeable increase in the number of laboratories with good performance in the two most recent exercises, observed both for biological and for sediment matrices. However, the determination of trace elements such as Cd, Cr, Pb and Hg in low level environmental samples still remains a major challenge to the analysts. For this reason and in order to assess the current performance of laboratories for low environmental levels of contaminants, the future intercomparison exercises will concentrate on low level sediment and fish samples

  2. Possibilities of High Resolution Inductively Coupled Plasma Optical Emission Spectrometry in the Determination of Trace Elements in Environmental Materials

    Directory of Open Access Journals (Sweden)

    Nikolaya Velitchkova

    2013-01-01

    Full Text Available This paper presents new quantitative data for the spectral interferences obtained by high resolution 40.68 MHz radial viewing inductively coupled plasma optical emission spectrometry (HR-ICP-OES in the determination of Zn, Cd, Sb, Cu, Mn, Pb, Sn, Cr, U, and Ba in environmental materials in the presence of a complex matrix, containing Al, Ca, Fe, Mg, and Ti. The -concept for quantification of spectral interferences was used. The optimum line selection for trace analysis of a variety of multicomponent matrices requires the choice of prominent lines, which are free or negligibly influenced by line interference problems. The versatility of -concept as basic methodology was experimentally demonstrated in the determination of trace of elements in soil and drinking water. The detection limits are lower in comparison with corresponding threshold concentration levels for soil and drinking water in accordance with environmental regulations. This paper shows the possibilities of present day ICP-OES equipment in the direct determination of trace elements (without preconcentration of impurities in environmental samples.

  3. Determination of trace element and heavy metal in black tea and tea leaves using x-ray fluorescence

    International Nuclear Information System (INIS)

    Salih, Mohamed Abualgasim Abdalhakam

    2016-08-01

    The aim of this study was to provide information about the trace element and heavy metals concentrations in black tea and tea leaves. 23 different samples were collected from the Sudanese local market. The collected samples were characterized as the most common used items in Sudan. The concentration of trace and heavy elements were determined using x-ray fluorescence (X RF) technique. The standard reference materials (IAEA-V-10) and hay (powder) were used to evaluate the accuracy of the analytical result. The measured values were found in agreement with the certified values. The elements determined were K, Ca, Cr, Mn, Fe, Ni, Cu, Zn, Pb, Br, Rb, and Sr. The average concentration of the elements is black tea were 2277.43, 7245.71, 1.11, 1025.29, 334.29, 6.88, 11.24, 9.47, 1.02, 7.08, 97.4 and 63.21 respectively while the average concentration of the elements in leaves tea were 2644.44, 8805.56, 1.02, 571.81, 295.44, 6.19, 10.69, 9.26, 0.91, 13.42, 63.03 and 67.14 respectively. The results showed an increase in the concentration of some elements such as calcium, chromium, manganese, iron, nickel, copper, zinc, bromine, rubidium and strontium (22500, 6.75, 48.9, 194, 4.37, 9,77, 24.9, 8.23, 7.79, 40,9) ppm respectively compared to certified values. Correlation between concentration of certain element and cluster analysis were preformed and the results compared with values of literature and the concentrations of some elements found to be similar.(Author)

  4. Determination of some toxic trace elements in Indian tobacco and its smoke

    International Nuclear Information System (INIS)

    Shaikh, A.N.; Khandekar, R.N.; Anand, S.J.S.; Mishra, U.C.

    1992-01-01

    Toxic trace metals like mercury, arsenic and cadmium have been determined in widely used Indian chewing tobacco and cigarette tobacco by neutron activation followed by sequential radiochemical separation (RNAA). Differential Pulse Anodic Stripping Voltammetry (DPASV) has been used for the estimation of lead, cadmium and copper in cigarette tobacco and its smoke aerosols. The reliability of the data has been assured by analyzing standard reference materials, bovine liver (NBS-1577) and orchard leaves (NBS-1571), and intercomparison of the Pb, Cd and Cu values by three techniques, namely, RNAA, DPASV and Energy Dispersive X-ray Fluorescence technique (EDXRF). The levels of Hg, Cd, As, Pb, and Cu in cigarette and chewing tobacco and the estimated intake of Cd, Cu and Pb to the smoker are presented and discussed. (author) 12 refs.; 3 tabs

  5. Determination of trace elements in kidneys, livers and brains of rats with sealer implants by ICP-MS

    International Nuclear Information System (INIS)

    Simsek, Neslihan; Akinci, Levent; Alan, Hilal; Gecör, Orhan; Özan, Ülkü

    2017-01-01

    Following root canal treatment, sealers may contact periapical tissue. The purpose of this study was to evaluate the systemic toxic effects of epoxy resin-based sealers (AH Plus and Obtuseal). Inductively coupled plasma-mass spectrometry (ICP-MS) was used to measure levels of trace elements (beryllium, magnesium, aluminium, calcium, chromium, arsenic and lead) in the brain, kidney and liver of rats. Twenty sterilized polyethylene tubes were then filled with AH Plus and Obtuseal and implanted into the dorsal subcutaneous tissue of 10 rats; three unoperated animals were used as a control group. After 45 days, the rats were sacrificed by cervical dislocation following anaesthesia, and brains, kidneys and livers were removed from all experimental animals. ICP-MS analysis was used to determine levels of trace elements. Data were analysed using Kruskal– Wallis and Connover post hoc tests. No significant differences were found in aluminium and calcium levels, but brains, kidneys and livers showed significantly higher amounts of magnesium and chromium than the corresponding controls. In the kidney and liver samples, arsenic levels were found to be higher than in the control group. Lead was detected at higher levels only in liver samples from the AH Plus group. Beryllium was not detected in any organ. It was concluded that AH Plus and Obtuseal release minimal quantities of trace elements when in contact with subcutaneous tissue, and further studies are needed to understand the systemic effects of these materials

  6. Determination of volatile trace elements in terrestrial minerals and lunar soils by RNAA

    International Nuclear Information System (INIS)

    Kraehenbuehl, U.; Wegmueller, F.

    1978-01-01

    A procedure is reported for the simultaneous determination of Au, Cd, Ge, Hg, In, Sb, Te and Zn in 5-50 mg aliquots of minerals and lunar soils. After irradiation with thermal neutrons the samples are dissolved in digestion bombs by HF/HClO 4 . Sulfide precipitates provide the necessary group separations. The purified elements are measured on Ge(Li) detectors. Accuracy and precision are generally better than 10%. (author)

  7. Determination by INAA of trace elements in Fucus sample (IAEA-0140)

    International Nuclear Information System (INIS)

    Salagean, M.; Pantelica, A.; Rusu, C.; Scarlat, A.

    1998-01-01

    The concentration of 25 elements (Al, As, Ba, Br, Ca, Ce, Co, Cr, Cs, Fe, Hf, Hg, K, La, Mg, Mn, Na, Rb, Sb, Sc, Sm, Sr, Th, V, Zn) in the marine algae Fucus sp. was determined by instrumental neutron activation analysis. This paper presents our contribution to an intercomparison exercise organized by IAEA. The results obtained in our laboratory, excepting Hg, are in very good or in good agreement with the intercomparison values

  8. Determination of atmospheric trace elements by INAA: An application of receptor modelling

    International Nuclear Information System (INIS)

    Tuncel, G.; Aras, N.K.; Yatin, M.

    1992-01-01

    The concentrations of twenty-eight elements in samples of airborne particulates from Ankara or a nearby area were determined by neutron activation analysis. It is hoped to use the data to provide information on the sources of the pollution in the city and to test emission inventory and dispersion models that will be developed in the course of the study. 14 refs, 6 tabs, figs

  9. Advanced functional materials in solid phase extraction for ICP-MS determination of trace elements and their species - A review.

    Science.gov (United States)

    He, Man; Huang, Lijin; Zhao, Bingshan; Chen, Beibei; Hu, Bin

    2017-06-22

    For the determination of trace elements and their species in various real samples by inductively coupled plasma mass spectrometry (ICP-MS), solid phase extraction (SPE) is a commonly used sample pretreatment technique to remove complex matrix, pre-concentrate target analytes and make the samples suitable for subsequent sample introduction and measurements. The sensitivity, selectivity/anti-interference ability, sample throughput and application potential of the methodology of SPE-ICP-MS are greatly dependent on SPE adsorbents. This article presents a general overview of the use of advanced functional materials (AFMs) in SPE for ICP-MS determination of trace elements and their species in the past decade. Herein the AFMs refer to the materials featuring with high adsorption capacity, good selectivity, fast adsorption/desorption dynamics and satisfying special requirements in real sample analysis, including nanometer-sized materials, porous materials, ion imprinting polymers, restricted access materials and magnetic materials. Carbon/silica/metal/metal oxide nanometer-sized adsorbents with high surface area and plenty of adsorption sites exhibit high adsorption capacity, and porous adsorbents would provide more adsorption sites and faster adsorption dynamics. The selectivity of the materials for target elements/species can be improved by using physical/chemical modification, ion imprinting and restricted accessed technique. Magnetic adsorbents in conventional batch operation offer unique magnetic response and high surface area-volume ratio which provide a very easy phase separation, greater extraction capacity and efficiency over conventional adsorbents, and chip-based magnetic SPE provides a versatile platform for special requirement (e.g. cell analysis). The performance of these adsorbents for the determination of trace elements and their species in different matrices by ICP-MS is discussed in detail, along with perspectives and possible challenges in the future

  10. Determination of radionuclides and trace elements in marine sediments and biota from the red sea coast

    International Nuclear Information System (INIS)

    Sirelkhatim, Dia Awad

    2002-09-01

    21.9 Bq/kg dry weight. Similarly, the highest concentration of 210 Po was met in Festive at 38.7 Bq/kg. There is no variation seen among algal species for 210 Pb uptake, however, converse to radium and polonium, Favites (coral) was found to contain the minimum concentration of lead (3.88). In most species there is preferential accumulation of polonium over its parent radium as indicated by 210 Po: 226 Ra activity ratio. On the other hand, 210 Po: 210 Pb activity concentration ratio revealed that coral species Favites (9.97) and the brown algae Sargassum (1.85) have a tendency to accumulate 210 Po over 210 Pb, while in the rest of species; this ratio is less than unity. For 239+240 Pu measured in marine algae and animal species, the molluscs species apparently shows the lowest plutonium uptake relative to other animal species analysed and the algal species display a greater tendency for accumulation of plutonium in contrast to animal species. The lowest activity concentration value of 90 Sr in mBq/kg dry weight was met in green algae species Entomorpha (40) and the highest value in coral species Favites (157.2). As regards 40 K, its activity concentration in marine biota ranges between 450 (molluscs species Tridacnica) to 6630 Bq/kg dry weight for the other molluscs species Lambia. For trace elements studied, marine algae species show the highest uptake for all elements except strontium, cerium, rubidium and arsenic. On the other hand, coral species Favites contains the maximum concentration of strontium and cerium whereas highest values for rubidium and arsenic are detected in molluscs species Lambia. Among algal species, the green algae Entomorpha show highest trace metals uptake strongly suggesting its suitability for utilization as an effective bioindicator for trace metals in the Red Sea environment. (Author)

  11. Worldwide Laboratory Comparison on the Determination of Trace Elements in IAEA-452 Biota Sample

    International Nuclear Information System (INIS)

    2012-01-01

    The Marine Environmental Studies Laboratory (MESL) of the International Atomic Energy Agency's Environment Laboratories (IAEA-NAEL) has the programmatic responsibility to provide assistance to Member States' laboratories in maintaining and improving the reliability of analytical measurement results, both in trace elements and organic pollutants. This is accomplished through the provision of reference materials of marine origin, validated analytical procedures, training in the implementation of internal quality control, and through the evaluation of measurement performance by the organization of worldwide and regional interlaboratory comparison exercises. For nearly thirty years, the MESL has conducted worldwide laboratory performance studies, also known as interlaboratory comparison. The results have been used to evaluate laboratory performance with respect to a wide range of organic and inorganic pollutants, including methyl mercury. This work has been conducted in collaboration with the UNEP Regional Seas Programme. The goal of interlaboratory comparison is to demonstrate the measurement capabilities of laboratories participating in interlaboratory comparisons (ILCs) and proficiency tests (PTs). The results from ILCs or PTs are of crucial interest for laboratories as these provide clear information of its measurement capabilities. It should be pointed out that the participation is either voluntary or forced by external requirements (e.g. legal, accreditation, control bodies). NAEL's interlaboratory comparison (ILC) and proficiency test (PT) schemes involve comparison of participant's results with an assigned value, which usually is delivered as a consensus value from the overall population of test results. Those exercises are designed to monitor and demonstrate the performance and analytical capabilities of the participating laboratories, and to identify gaps and problem areas where further development is needed. Continued membership has benefits in training and

  12. Assessment and modifications of digestion procedures to determine trace elements in urine of hypertensive and diabetes mellitus patients

    Directory of Open Access Journals (Sweden)

    Awad Abdalla Momen

    2013-01-01

    Full Text Available Context: There is accumulating evidence that the metabolism of several trace elements like Cr, Cu, Pb, Cd, Co, Mn and Zn might have specific roles in the pathogenesis and progress of many diseases like hypertension (HTN and diabetes mellitus (DM. Objectives: To provide a fast, efficient, sensitive, and reliable analytical procedure for trace element determination in urine samples of HTN and DM patients using inductively coupled plasma optical emission spectrometry (ICP-OES. Setting and Design: The ICP-OES operating conditions were optimised and carefully selected in order to maximise the sensitivity, precision and accuracy. Factors affecting analytical and biological variability of the concentrations under study were discussed and carefully optimised. Materials and Methods: Different digestion procedures with acids and oxidising reagents were tested. The suitable procedure ICP-OES was selected, carefully modified and applied. The validity and accuracy of the different elements were determined by spiking of samples with known amounts of multi-element standard solution. Statistical Analysis: Student t-test and analysis of variance (ANOVA test were used for analysis. Microsoft Excel was used to assess the significance of the difference between variables. The concentrations obtained were expressed as mean value ± standard deviation (P = 0.05. Results: The results of this study showed that the mean concentrations of Cd, Zn, Pb, Cu, Cr and Mn in urine from both HTN (study group A and DM (study group B patients were higher than the corresponding values observed in the control group. However, while the mean value of Co was low as compared to the control group, the differences found were not significant (P = 0.05. Conclusion: The method used had excellent sensitivity, multi-element data could be obtained with very short acquisition time. The elements Cr, Cd, Pb and Zn might have specific roles in the pathogenesis and progress of HTN and DM. Further

  13. Freeze dried samples of volcanic gases - a new method for the determination of trace elements by NAA

    International Nuclear Information System (INIS)

    Bichler, M.; Sortino, F.

    1997-01-01

    A new routine technique for the determination of trace elements in volcanic gases by NAA is presented. For time and money saving reasons this method is applicable to samples, collected by the conventional method. This technique uses evacuated glass bottles, partly filled with NaOH solution to absorb acidic gas components and CO 2 , which is the main constituent of the incondensable gas fraction at ambient conditions. The application of NAA to samples collected by this method shows two main sources of difficulties: drying of NaOH without loosing volatile elements of interest (in particular Hg and Se) and the high activities of 24 Na after neutron irradiation. The first can be avoided by liquid irradiation, thereby limiting the irradiation time, the second excludes the determination of short and medium lived nuclides because of the high γ-background due to 24 Na. A new freeze drying technique enables the application of long irradiation times and therefore the use of long-lived activation products for analysis. The samples of volcanic gases were collected at the fumarole fields of La Fossa volcano on the island Vulcano. Southern Italy. This technique allows very sensitive determinations of trace elements in volcanic gases and adds highly valuable information to the understanding and modeling of volcanic gas sources. (orig.)

  14. Determination of trace elements in some Nigerian vegetable based oils by neutron activation analysis

    International Nuclear Information System (INIS)

    Obi, A.L.; Jonah, S.A.; Umar, I.

    2001-01-01

    The concentrations of some essential micronutrient elements leading to short-lived activation products in four Nigerian vegetable based oils (palm oil, palm kernel oil, sheabutter and groundnut oil) have been determined by neutron activation analysis using a small research reactor. One sample of each material was analysed and presented as an introduction for further investigations. Results indicate that the concentration range of the elements are 19.4-44.0 μg/g for Al; 30.0-81.0 μg/g for Ca; 11.9-60.4 μg/g for Cl; 1.43-5.96 μg/g for Cu; 7.3-28.1 μg/g for Mg; 0.47-1.69 μg/g for Mn; 17.5-72.8 μg/g for Na and 0.04-0.07 μg/g for V. The experimental procedure is suitable for routine determination of micronutrient element in foods for control and monitoring purposes. (author)

  15. Determination of trace elements in Tillandsia usneoides by neutron activation analysis for environmental biomonitoring

    International Nuclear Information System (INIS)

    Figueiredo, A.M.G.; Saiki, M.; Ticianelli, R.B.; Domingos, M.; Alves, E.S.; Markert, B.

    2001-01-01

    Neutron activation analysis was applied to the determination of the elements Al, As, Ba, Br, Cl, Co, Cr, Fe, K, Mg, Mn, Mo, Na, Rb, Sb, Sc, Ti, Th, V, Zn and the rare earths La, Ce, Nd, Sm, Eu, Tb and Yb in the epiphytic bromeliad Tillandsia usneoides. The samples were collected at an unpolluted area and exposed in different sites of the city of Sao Paulo, Brazil, and in a control site outside Sao Paulo. The results obtained showed an accumulation of Al, As, Cr, Fe, Mo, Sb, Ti, V and Zn elements in Tillandsia usneoides exposed in polluted sites, indicating a promising potential of this species as a biomonitor of air pollution in Sao Paulo. (author)

  16. Use of activation analysis method for determining trace elements in human nail clippings

    International Nuclear Information System (INIS)

    Aguiar, Amilton Reinaldo; Saiki, Mitiko

    1999-01-01

    This work presents results obtained in nail clipping samples analyses. These nail samples were collected from healthy group of individuals and from patients with cystic fibrosis disease. Irradiation of nail clippings was carried out with a thermal neutron flux from 10 11 to 10 13 n.cm -2 .s -1 at the IEA-R1m nuclear research reactor and the elements Al, As, Br, Ca, cd, Cl, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Se and Zn were determined. The results obtained for healthy group were within the range of concentrations published, for normal population. However for several elements, the group of patients presented higher concentrations than those presented for healthy individuals. The precision and the accuracy of the results were evaluated by analyzing reference materials NIST 1577b Bovine Liver and 1566a Oyster Tissue. (author)

  17. A critical review of nuclear activation techniques for the determination of trace elements in atmospheric aerosols, particulates and sludge samples

    International Nuclear Information System (INIS)

    Dams, R.

    1992-01-01

    Activation analysis is one of the major techniques for the determination of many minor and trace elements in a large variety of solid environmental and pollution samples, such as atmospheric aerosols, particulate emissions, fly ash, coal, incineration ash and sewage sludge, etc. Neutron activation analysis of total, inhalable or respirable airborne particulate matter collected on a filter or in a cascade impactor on some substrate, is very popular. By Instrumental Neutron Activation Analysis (INAA) up to 45 elements can be determined. The irradiation and counting procedures can be adapted to optimize the sensitivity for particular elements. The precision is largely governed by counting statistics and a high accuracy can be obtained after calibration with multi-elemental standards. Radiochemical Neutron Activation Analysis (RNAA) is applied only when extremely low limits of determination are required. Instrumental Photon Activation Analysis (IPAA) is complementary to INAA, since some elements of environmental interest can be determined which do not produce appropriate radionuclides by neutron irradiation. Charged Particle Activation Analysis (CPAA) is used in particular circumstances such as for certification purposes or coupled to radiochemical separations for extremely low concentrations. (author)

  18. Determination of trace elements in eyeshadow, face powder and rouge make-up cosmetics by neutron activation analysis

    International Nuclear Information System (INIS)

    Kanias, G.D.

    1985-01-01

    Some trace elements exist in cosmetics due to the mineral origin of their raw materials and there is no information about their concentration levels in these products. Instrumental neutron activation analysis was applied to determine the elements: cerium, cesium, europium, hafnium, lanthanum, lutetium, potassium, rubidium, samarium, scandium, sodium, tantalum, terbium, tungsten and ytterbium in eyeshadow, face powder and rouge make-up cosmetic products from the Greek market. According to the results, a wide range of values was found between the three examined cosmetics as well as between the different samples belonging to the same kind of cosmetics. This probably could be attributed to the various manufacturers of the analyzed samples. Moreover, the use of neutron activation analysis as a suitable routine method is discussed for the control of some elements which must not be contained in cosmetics. (author)

  19. Determination of seven trace elements in human milk, powdered cow's milk and infant foods by neutron activation analysis

    International Nuclear Information System (INIS)

    Grimanis, A.P.; Vassilaki-Grimani, M.; Alexiou, D.; Papadatos, C.

    1979-01-01

    The purpose of this study was to apply neutron activation analysis to the determination of seven trace elements (Co, Cr, Cu, Se, Zn, Rb and As) in colostrum, transitional and mature human milk as well as in powdered cow's milk and commercial infant foods, and thus to find out whether non-breast-fed infants received the same or different amounts of these trace elements as breast-fed ones. Ranges and averages for trace elements in mature human milk, expressed as microgrammes per gramme wet weight, varied as follows: Cr 0.018-0.040 and 0.027; Co 0.0013-0.0030 and 0.0020; Cu 0.38-0.50 and 0.46; Se 0.011-0.022 and 0.015; Zn 1.4-1.7 and 1.5; Rb 0.60-0.66 and 0.63; and As 0.0016-0.0060 and 0.0032. The mean concentrations of the essential trace elements Zn, Se, Cu, Cr and Co in colostrum were, respectively, 3.7, 3.2, 2.4, 1.8 and 1.7 times higher than those in mature human milk. No significant differences in Rb and As concentrations were found between colostrum and mature milk. Average values of Zn and Cu in transitional human milk were, respectively, 3.4 and 1.5 times higher than in mature milk. No significant differences for the rest of the elements were found between these two milk samples. The two milk formulas, half-cream and humanized, contained higher mean concentrations of Zn, Rb and As and similar or lower concentrations of Cr, Co and Se than mature human milk. Half-cream is deficient in Cu; mature human milk contains about 9 times more Cu than the half-cream cow's milk. Humanized milk contains a similar mean concentration of Cu as the mature milk. All examined infant foods contained similar or higher concentrations of all elements determined than did the mature human milk

  20. Determination of trace elements in cardiotonic drugs by neutron activation analysis

    International Nuclear Information System (INIS)

    Kanias, G.D.

    1980-01-01

    Potassium may be intimately involved in the action of cardiac glycosides. Chlorine and potassium also act as diuretics. The elements chlorine, manganese, potassium and sodium are determined by instrumental neutron activation analysis in the cardiotonic drugs (pills, injections, water solutions). It has been found that there is a wide variation among the different values for manganese, sodium and chlorine while for potassium values are relatively constant. Results are discussed from the pharmacological point of view. It is proposed to study the role of manganese in cardiotonic drugs as well as the effect of potassium addition in oral pharmaceutical form of cardiotonic drugs in decreasing the toxicity of cardiac glycosides. (author)

  1. Trace and essential elements determination in baby formulas milk by INAA and k0-INAA techniques

    International Nuclear Information System (INIS)

    Lylia Hamidatou; Hocine Slamene; Tarik Akhal; Alaa Boulegane

    2014-01-01

    As a part of the food analysis program executed at Es-Salam research reactor by neutron activation analysis laboratory, the concentration of As, Ba, Br, Ca, Fe, K, La, Rb and Zn in baby formulas milk have been determined by using INAA and k 0 -NAA techniques. It was found that the concentration of all elements obtained by both techniques was relatively identical for the three brands of the 0-6 and 6-12 months of analyzed samples. In addition, the analytical results have been compared with those given by producers. (author)

  2. Simultaneous determination of twelve trace elements in estuarine and sea water using pre-irradiation chromatography

    International Nuclear Information System (INIS)

    Greenberg, R.R.; Kingston, H.M.

    1982-01-01

    A procedure is described for the preconcentration of 100 m of estuarine and seawater into a solid sample using Chelex-100 resin. This solid sample weighs less than half a gram and contains the transition metals and many other elements of interest, but is essentially free from the alkali metals, the alkaline earth metals, and the halogens. The concentrations of Co, Cr, Cu, Fe, Mn, Mo, Ni, Sc, Th, U, V and Zn have been determined in seawater when this procedure was coupled to neutron activation analysis. (author)

  3. Determination of trace elements in seawater by air-flow injection/ICP-MS with chelating resin preconcentration

    International Nuclear Information System (INIS)

    Lee, Kyue-Hyung; Ohshima, Mitsuko; Motomizu, Shoji

    2002-01-01

    Multielement determination of major to trace metals in a deep seawater malt was accomplished by inductively coupled plasma-mass spectrometry (ICP-MS) together with inductively coupled plasma-atomic emission spectrometry (ICP-AES). Major elements, such as Na, K, Mg, and Ca, were measured by ICP-AES and normal continuos nebulization ICP-MS after sample dilution by 10 3 -10 6 fold. Fifteen trace elements in the concentrated metal solutions pretreated with cation-exchange resin or chelating resin could be simultaneously determined by air-flow injection/ICP-mass spectrometry (AFI/ICP-MS). Since the injection volume for AFI/ICP-MS was 25 μl, final samples volumes less than 500 μl were enough for several replicate measurements. Three different preconcentration methods assisted with AFI/ICP-MS were examined and could be successfully applied to a deep seawater malt. The analytical results of rate earth elements (REEs) and Co, Ni, Cu, Zn, Cd, and Pb obtained by AFI/ICP-MS coupled with disk filtration method using iminodiacetate (IDA)-type chelating resin were favorably agreed with the data obtained by AFI/ICP-MS coupled with column preconcentration method using chitosan-based chelating resin. (author)

  4. Determination and correlation of spatial distribution of trace elements in normal and neoplastic breast tissues evaluated by μ-XRF

    International Nuclear Information System (INIS)

    Silva, M.P.; Oliveira, M.A.; Poletti, M.E.

    2012-01-01

    Full text: Some trace elements, naturally present in breast tissues, participate in a large number of biological processes, which include among others, activation or inhibition of enzymatic reactions and changes on cell membranes permeability, suggesting that these elements may influence carcinogenic processes. Thus, knowledge of the amounts of these elements and their spatial distribution in normal and neoplastic tissues may help in understanding the role of these elements in the carcinogenic process and tumor progression of breast cancers. Concentrations of trace elements like Ca, Fe, Cu and Zn, previously studied at LNLS using TXRF and conventional XRF, were elevated in neoplastic breast tissues compared to normal tissues. In this study we determined the spatial distribution of these elements in normal and neoplastic breast tissues using μ-XRF technique. We analyzed 22 samples of normal and neoplastic breast tissues (malignant and benign) obtained from paraffin blocks available for study at the Department of Pathology HC-FMRP/USP. From the blocks, a small fraction of material was removed and subjected to histological sections of 60 μm thick made with a microtome. The slices where placed in holder samples and covered with ultralen film. Tissue samples were irradiated with a white beam of synchrotron radiation. The samples were positioned at 45 degrees with respect to the incident beam on a table with 3 freedom degrees (x, y and z), allowing independent positioning of the sample in these directions. The white beam was collimated by a 20 μm microcapillary and samples were fully scanned. At each step, a spectrum was detected for 10 s. The fluorescence emitted by elements present in the sample was detected by a Si (Li) detector with 165 eV at 5.9 keV energy resolution, placed at 90 deg with respect to the incident beam. Results reveal that trace elements Ca-Zn and Fe-Cu could to be correlated in malignant breast tissues. Quantitative results, achieved by Spearman

  5. Determination of trace elements in lichen samples by neutron activation analysis

    International Nuclear Information System (INIS)

    Saiki, Mitiko; Coccaro, D.M.B.; Vasconcellos, M.B.A.; Marcelli, M.P.

    1999-01-01

    Epiphytic lichens have been used as bioindicators of environmental pollution studies because of their ability to accumulate metals present in the atmosphere at very low concentrations. In this work, experimental conditions for collection and preparation of the lichen samples as well as the experimental procedure for neutron activation analysis were established in order to obtain reliable and useful data for environmental monitoring purposes. Lichen samples were collected from the barks of trees. They were first examined in a stereo microscope, cleaned and then they were washed with water, freeze-dried and ground for analysis. Out of the five species Usnea sp, Parmotrena tinctorum, Canoparmelia caroliniana, Parmotrema sanctiangeli and Canoparmelia texana analysed, the latter was chosen for this work since this species is very abundant on the Brazilian territory except for the coast. The samples and synthetic standards of elements were irradiated at the IEA-R1 nuclear reactor and the concentrations of the elements Al, As, Br, Ca, Cd, Cl, Co, Cr, Cs, Fe, K, lanthanides, Mg, Mn, Na, Rb, Sb, Sc, Se, Th, U, V and Zn were determined by using short and long irradiations. Results obtained in the washed and unwashed lichen samples showed that the cleaning with water can be used in order to eliminate adhering materials. Indeed, most of elements of interest for the environmental contamination accumulated by the lichens were not removed. The study of the influence of the age of the lichen indicated that its elemental concentrations increase with its age or with the length of exposure. Results obtained for lichens collected from four different trees in the same sampling area varied from about 3.4 to 50%. The homogeneity of the sample was checked by analyzing replicates. The precision and the accuracy of the method were evaluated by analyzing IAEA 336 Lichen and NIST 1752 Citrus Leaves. (author)

  6. Enrichment method for trace amounts of rare earth elements using chemofiltration and XRF determination

    International Nuclear Information System (INIS)

    De Vito, I.E.; Olsina, R.A.; Masi, A.N.

    2000-01-01

    A preconcentration method for subsequent determination of rare earth elements (REE) by X-ray fluorescence (XRF) spectrometry was developed. The method is based on using (o-[3,6-disulfo-2-hydroxy-1-naphthylazo]-benzenearsonic acid) (Thorin) as a complexing agent which is retained on a polyamide membrane by a chemofiltration process. The pH dependence of the chemofiltration of these metal ions on the membrane and other variables, such as flow-rate, contact time, kinetic of complex formation, etc. were determined. The membrane containing the chemofiltrate formed a thin film, which eliminated the interelemental effects when measured by XRF. The detection limits were 23, 23 and 49 ng/mL for Sm(III), Eu(III) and Gd(III), respectively. High enrichment factors were obtained. The method was successfully applied to the preconcentration of Sm(III), Eu(III) and Gd(III) from different samples. (orig.)

  7. Determination of trace elements in various kinds of bean by X-ray spectrometric techniques (1995-96)

    International Nuclear Information System (INIS)

    U Tin Maung Kyi; U Wai Zin Oo

    2001-01-01

    Various kinds of bean such as Peanut, Gram Whole, Black Eye Bean, Small Red Bean, Lab Lab Bean, Green Mung Bean, Filed Pea, Seasame Seed, Sultani, Maize, Butter Bean, Dolichos Lab Lab, Toor Whole, Small Yellow Bean, Cow Pea have been collected and analysed by EDXRF analysis for trace elements. The measurement system consists of a Cd-109 annual excitation source, a Si (Li) detector, H V power supply, a spectrometry amplifier, a multichannel analyser and a personal computer. The samples were prepared as pressed pellets and measured by Emission Transmission Technique. The accuracy was determined by analysing standard reference material, SOIL-7 form IAEA. (author)

  8. Trace elements determination in silicon and ferrosilicon reference materials by instrumental neutron activation analysis method

    International Nuclear Information System (INIS)

    Moreira, Edson Goncalves; Vasconcellos, Marina Beatriz Agostini; Saiki, Mitiko; Iamashita, Celia Omine

    2002-01-01

    The use of certified reference materials, CRM, is of uppermost importance in the rastreability realization of the measurement process. At times, CRM use is restricted by the non existence of a suitable CRM with similarity to the sample in respect to matrix composition or with element levels in different orders of magnitude. IPT Chemical Division launched a project to prepare a metallic silicon CRM, due to the requirements of the industries in this field. To characterize this new CRM, IPEN Nuclear Reactor Center is able to perform instrumental neutron activation analysis, INAA, a very suitable method for silicon matrix samples because they produce basically the short lived radionuclide 3 1 Si under thermal neutrons flux, which after radioactive decay, does not interfere in the determination of other elements. In this paper, it is presented the determination of As, Br, Co, Cr, K, Eu, Fe, La, Mn, Na Nb, Sb, Sm, Sc, Th, Tb, U, V, W and Yb in silicon CRM NBS SRM 57; ferrosilicon CRM IPT 56; IPT 70; NBS SRM 58a; NBS SRM 59a and silicon RM under preparation IPT 132. From the results, the accuracy and the precision of the process were assessed. (author)

  9. Automated energy-dispersive x-ray determination of trace elements in stream sediments

    International Nuclear Information System (INIS)

    Hansel, J.M.; Martell, C.J.

    1977-01-01

    Nickel, copper, tungsten, lead, bismuth, niobium, silver, cadmium, and tin are determined in stream sediments using a computer-controlled energy-dispersive x-ray fluorescence system. The system consists of an automatic 20-position sample changer, a silicon lithium-drifted detector, a pulsed molybdenum transmission-target x-ray tube, a multichannel analyzer, and a minicomputer. Samples are analyzed as minus 325-mesh powders. A computer program positions the samples, unfolds overlapping peaks, determines peak intensities for each element, and calculates the ratio of the intensity of each peak to that of the molybdenum Kα Compton peak. Concentrations of each element are then calculated using equations obtained by analyzing prepared standards. Detection limits range from 5 ppM for silver, cadmium, lead, and bismuth to 20 ppM for niobium. The relative standard is 10 percent or less at the 100-ppM level and 20 percent at the 20-ppM level. Samples can be analyzed at the rate of sixty per day

  10. Determination of several trace elements in silicate rocks by an XRF method with background and matrix corrections

    International Nuclear Information System (INIS)

    Pascual, J.

    1987-01-01

    An X-ray fluorescence method for determining trace elements in silicate rock samples was studied. The procedure focused on the application of the pertinent matrix corrections. Either the Compton peak or the reciprocal of the mass absorption coefficient of the sample was used as internal standard for this purpose. X-ray tubes with W or Cr anodes were employed, and the W Lβ and Cr Kα Compton intensities scattered by the sample were measured. The mass absorption coefficients at both sides of the absorption edge for Fe (1.658 and 1.936 A) were calculated. The elements Zr, Y, Rb, Zn, Ni, Cr and V were determined in 15 international reference rocks covering wide ranges of concentration. Relative mean errors were in many cases less than 10%. (author)

  11. Trace element content of human hair determined using neutron activation analysis as monitor of exposure effects to environmental metals

    International Nuclear Information System (INIS)

    Dutkiewicz, T.; Paprotny, W.; Sokolowska, D.; Kulka, E.; Woyciechowska, E.; Dybczynski, R.; Sterlinski, S.

    1978-01-01

    Determination of 17 trace elements, mainly metals, in small hair samples by neutron activation analysis was elaborated. The number of elements determined in one sample made it possible to assess quickly the exposure of human population in a given region. The hair samples after careful washing according to procedure elaborated previously were irradiated in high reactor neutron flux (approximately 10 14 n.cm -2 .s -1 ). The activities of samples were measured three times (for different decay times) by means of Ge(Li) gamma-ray spectrometer. A new version of the comparator technique, called a triple-single comparator method, was applied for quantitative analysis. The statistical methods used for planning of sampling and preliminary results on evaluation of analytical data are also described. (author)

  12. Determination of trace elements in paints by direct sampling graphite furnace atomic absorption spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Bentlin, Fabrina R.S. [Instituto de Quimica, Universidade Federal do Rio Grande do Sul, UFRGS, 91501-970 Porto Alegre, RS (Brazil); Pozebon, Dirce [Instituto de Quimica, Universidade Federal do Rio Grande do Sul, UFRGS, 91501-970 Porto Alegre, RS (Brazil)], E-mail: dircepoz@iq.ufrgs.br; Mello, Paola A.; Flores, Erico M.M. [Departamento de Quimica, Universidade Federal de Santa Maria, UFSM, 97105-900 Santa Maria, RS (Brazil)

    2007-10-17

    A direct sampling graphite furnace atomic absorption spectrometric (DS-GFAAS) method for the determination of Cd, Pb, Cr, Ni, Co and Cu in paints has been developed. Serigraphy, acrylic and tattoo paints were analysed. Approaches like pyrolysis and atomization temperatures, modifiers and sample mass introduced in the atomizer were studied. Quantification was performed using calibration curves measured with aqueous standard solutions pipetted onto the platform. The sample mass introduced in the graphite tube ranged from 0.02 to 8.0 mg. Palladium was used as modifier for Cd, Pb and Cu, while Mg(NO{sub 3}){sub 2} was used for Co. For Ni determination, the graphite platform was covered with carbon powder. The characteristic masses of Cd, Pb, Cr, Ni, Co and Cu were 1.4, 22.5, 7.9, 11.0, 9.6 and 12.5 pg, while the limits of detection were 0.0004, 0.001, 0.03, 0.22, 0.11 and 0.05 {mu}g g{sup -1} of Cd, Pb, Cr, Ni, Co and Cu, respectively. The accuracy was determined by comparison of the results with those obtained by inductively coupled plasma mass spectrometry (ICP-MS) and graphite furnace atomic absorption spectrometry (GFAAS), using liquid sampling of digests. For matrix characterization, major and minor elements (Al, Mg, Ba, Ca, Cr, Cu, Pb, Sr, Ti and Mg) were determined by inductively coupled plasma optical emission spectrometry (ICP OES)

  13. Determination of trace elements in paints by direct sampling graphite furnace atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Bentlin, Fabrina R.S.; Pozebon, Dirce; Mello, Paola A.; Flores, Erico M.M.

    2007-01-01

    A direct sampling graphite furnace atomic absorption spectrometric (DS-GFAAS) method for the determination of Cd, Pb, Cr, Ni, Co and Cu in paints has been developed. Serigraphy, acrylic and tattoo paints were analysed. Approaches like pyrolysis and atomization temperatures, modifiers and sample mass introduced in the atomizer were studied. Quantification was performed using calibration curves measured with aqueous standard solutions pipetted onto the platform. The sample mass introduced in the graphite tube ranged from 0.02 to 8.0 mg. Palladium was used as modifier for Cd, Pb and Cu, while Mg(NO 3 ) 2 was used for Co. For Ni determination, the graphite platform was covered with carbon powder. The characteristic masses of Cd, Pb, Cr, Ni, Co and Cu were 1.4, 22.5, 7.9, 11.0, 9.6 and 12.5 pg, while the limits of detection were 0.0004, 0.001, 0.03, 0.22, 0.11 and 0.05 μg g -1 of Cd, Pb, Cr, Ni, Co and Cu, respectively. The accuracy was determined by comparison of the results with those obtained by inductively coupled plasma mass spectrometry (ICP-MS) and graphite furnace atomic absorption spectrometry (GFAAS), using liquid sampling of digests. For matrix characterization, major and minor elements (Al, Mg, Ba, Ca, Cr, Cu, Pb, Sr, Ti and Mg) were determined by inductively coupled plasma optical emission spectrometry (ICP OES)

  14. [Rapid determination of major and trace elements in the salt lake clay minerals by X-ray fluorescence spectrometry].

    Science.gov (United States)

    Wang, Xiao-Huan; Meng, Qing-Fen; Dong, Ya-Ping; Chen, Mei-Da; Li, Wu

    2010-03-01

    A rapid multi-element analysis method for clay mineral samples was described. This method utilized a polarized wave-length dispersive X-ray fluorescence spectrometer--Axios PW4400, which had a maximum tube power of 4 000 watts. The method was developed for the determination of As, Mn, Co, Cu, Cr, Dy, Ga, Mo, P, Pb, Rb, S, Sr, Ni, ,Cs, Ta, Th, Ti, U, V, Y, Zn, Zr, MgO, K2O, Na2O, CaO, Fe2O3, Al2O3, SiO2 and so on. Thirty elements in clay mineral species were measured by X-ray fluorescence spectrometry with pressed powder pellets. Spectral interferences, in particular the indirect interferences of each element, were studied. A method to distinguish the interference between each other periodic elements in element periodic table was put forward. The measuring conditions and existence were mainly investigated, and the selected background position as well as corrected spectral overlap for the trace elements were also discussed. It was found that the indirect spectral overlap line was the same important as direct spectral overlap line. Due to inducing the effect of indirect spectral overlap, some elements jlike Bi, Sn, W which do not need analysis were also added to the elements channel. The relative standard deviation (RSD) was in the range of 0.01% to 5.45% except three elements Mo, Cs and Ta. The detection limits, precisions and accuracies for most elements using this method can meet the requirements of sample analysis in clay mineral species.

  15. Simultaneous determination of macronutrients, micronutrients and trace elements in mineral fertilizers by inductively coupled plasma optical emission spectrometry

    International Nuclear Information System (INIS)

    Oliveira Souza, Sidnei de; Silvério Lopes da Costa, Silvânio; Santos, Dayane Melo; Santos Pinto, Jéssica dos; Garcia, Carlos Alexandre Borges

    2014-01-01

    An analytical method for simultaneous determination of macronutrients (Ca, Mg, Na and P), micronutrients (Cu, Fe, Mn and Zn) and trace elements (Al, As, Cd, Pb and V) in mineral fertilizers was optimized. Two-level full factorial design was applied to evaluate the optimal proportions of reagents used in the sample digestion on hot plate. A Doehlert design for two variables was used to evaluate the operating conditions of the inductively coupled plasma optical emission spectrometer in order to accomplish the simultaneous determination of the analyte concentrations. The limits of quantification (LOQs) ranged from 2.0 mg kg −1 for Mn to 77.3 mg kg −1 for P. The accuracy and precision of the proposed method were evaluated by analysis of standard reference materials (SRMs) of Western phosphate rock (NIST 694), Florida phosphate rock (NIST 120C) and Trace elements in multi-nutrient fertilizer (NIST 695), considered to be adequate for simultaneous determination. Twenty-one samples of mineral fertilizers collected in Sergipe State, Brazil, were analyzed. For all samples, the As, Ca, Cd and Pb concentrations were below the LOQ values of the analytical method. For As, Cd and Pb the obtained LOQ values were below the maximum limit allowed by the Brazilian Ministry of Agriculture, Livestock and Food Supply (Ministério da Agricultura, Pecuária e Abastecimento — MAPA). The optimized method presented good accuracy and was effectively applied to quantitative simultaneous determination of the analytes in mineral fertilizers by inductively coupled plasma optical emission spectrometry (ICP OES). - Highlights: • Determination of inorganic constituents in mineral fertilizers was proposed. • Experimental design methodology was used to optimize analytical method. • The sample preparation procedure using diluted reagents (HNO 3 and H 2 O 2 ) was employed. • The analytical method was satisfactorily to the determination of thirteen elements. • The ICP OES technique can be

  16. Trace elements in Turkish tea leaves determined by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Demiralp, R.

    1985-01-01

    The concentrations of the elements As, Sb, Zn, Co, which are closely related to human health and disorder, was determined by means of INAA in seven of the most commonly used brands of tea. Samples and standards were irradiated 10 min and 2 hrs at pneumatic system and central thimble in the TRIGA MARK-11 research reactor. After irradiation the activities were measured with a coaxial Ge detector coupled to a spectroscopic amplifier. A Cambera 90 model multichannel analyser with an 8K memory was used for pulse hight analysis. The system has a resolution of 2,0 KeV for 1332,5 KeV gamma ray of 60 Co with peak to Compton ratio of 43:1 and efficiency of 18 relative to the 3'' x 3'' NaI(Tl) crystal. Results of the study were presented

  17. Determination of trace elements in aerosols from the antarctic peninsula by neutron activation analysis

    International Nuclear Information System (INIS)

    Loureiro, A.L.M.

    1989-01-01

    In this work the neutron activation method was applied to carry out multielemental analysis in aerosols collected in the Brazilian Station 'Comandante Ferraz', located on King George Island, at the Antarctic Peninsula, during 1986 and 1987. The aerosols were collected on 0.45 μum Millipore-MF filter paper, type HA. The analytical method was based on the simultaneous irradiations of filters and synthetic standards in the IEA-R1 nuclear reactor under a thermal neutron flux of about 10 12 n cm -2 s -1 . The induced radioactivity was measured in a gamma ray spectrometer after suitable cooling times. Samples were irradiated twice, with irradiation times varying from 5 minutes to 24 hours. The elements Na, Al, Cl, K, Ca, Sc, V, Mn, Fe, Zn, Br, Sb, La, Au and Th were determined with concentration levels from ng/m 3 to pg/m 3 [pt

  18. Non-destructive determination of trace-element concentrations. Annual progress report, September 1977

    International Nuclear Information System (INIS)

    Gordon, G.E.; Zoller, W.H.; Walters, W.B.

    1977-01-01

    Equipment has been assembled at the National Bureau of Standards (NBS) reactor by the University of Maryland group in cooperation with the NBS staff in order to initiate studies of a new analytical technique, neutron-capture prompt γ-ray activation analysis. According to this technique one observes prompt γ-rays while the sample is under neutron bombardment, rather than observing γ rays from decay of radioactive species produced. It is expected that this technique will make possible the non-destructive determination of a number of elements in several classes of samples that cannot be measured by present analytical methods. A beam thimble has been built for insertion into the reactor. A beam stop and target holder have been designed and are under construction. The detection system has been designed and is on order. The pulse-height analyzer system has been obtained and debugged and most of the software needed has been written

  19. Determination of some trace elements in biological materials using the short living isotopes

    International Nuclear Information System (INIS)

    Taskaev, E.

    1985-01-01

    A method for determination of V, Cu, Rb, Mo and K in breast cancer tumors is described. Samples were irradiated with ICIS pneumatic irradiation system of University of London Reactor Centre for 5 min. with mixed neutron flux: 1,7.10 1 2 thermal neutrons.cm -2 .s -1 and 9.10 11 fast neutrons.cm -2 .s -1 . Wet ashing procedure of Byrne and Kosta was used for the dissolution. Consecutive separation procedures of V and Mo, Cu, Mn, K and Rb, followed by counting and activity measuring were carried out. In order to study the chemical yields for all the elements both animal and plant matrixes were used. The error of 3% ( 0.05 confidence level) for single determination of chemical yield was chosen as the highest value acceptable. The possibility of using 137-Cs tracer for K and Rb chemical yield determination was also checked. To check the whole procedure the standard reference materials SRM-1577 Bovine Liver, SRM-1571 Orchard Leaves and Bowen's Kale were analysed

  20. Laser ablation inductively coupled plasma mass spectrometry for the determination of trace elements in soil

    International Nuclear Information System (INIS)

    Lee Yiling; Chang Chaochiang; Jiang Shiuhjen

    2003-01-01

    Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been applied to the determination of Cr, Cu, Zn, Cd and Pb in soil samples. The dried soil powder was pressed into a pellet for LA-ICP-MS analysis. Triton X-100 was added to work as the modifier to enhance the ion signals. The influences of instrument operating conditions (LA and ICP-MS) and pellet preparation on the ion signals were reported. For Cr determination, the ICP-MS was operated under the dynamic reaction cell mode which alleviated the mass overlap interference. Standard addition method and isotope dilution method were used for the quantitation work. The powder sample was spiked with suitable amounts of element standards and/or enriched isotopes, well-mixed, dried and then pressed into a pellet for LA-ICP-MS analysis. This method has been applied to determine Cr, Cu, Zn, Cd and Pb in NIST SRM 2711 Montana soil and NIST SRM 2709 San Joaquin soil reference materials. The analysis results were in agreement with the certified values. The precision between sample replicates was better than 5% with LA-ICP-MS method. Detection limits estimated from standard addition curves were approximately 0.9, 2, 9, 0.7 and 0.3 ng g -1 for Cr, Cu, Zn, Cd and Pb, respectively

  1. The determination of trace element changes in Downer Cow Syndrome by nuclear methods

    International Nuclear Information System (INIS)

    Popescu, Ion V.; Iordan, M.; Dima, Gabriel; Stihi, Claudia; Oros, C.; Badica, Teodor

    2000-01-01

    Various biomedical applications of nuclear methods (especially Particle Induced X-Ray Emission PIXE) were developed in an extensive study by Johansson and Campbell.The causes of Downer Cow Syndrome (DCS) are the metabolic and toxic perturbation. The DCS is included in the largest group of dismineralisations with some other diseases of cattle like hypomagnesaemia. It is precisely a disease generated by the superposition of some factors. One of them is the type and the chemical composition of soil and plants involved in nutrition. Other factors are the chemical processes used in food preparation as well as some technological factors like: the husbandry system and the characteristics of the locally habitation and individual factors (the species, the productive type and physiological state). The origin of this syndrome is uncertain but the clinical experience indicates that the DCS is enhanced by the hypocalcaemic paresis of parturition. The diminution of some nutritive elements from food can be a cause of DCS. The cattle are more sensitive to the diminution of P in food in comparison to the diminution of Ca. An increase of this ratio determines unfortunately the Ca absorption because of the deficit of vitamin D. In the present study the elemental and enzymatic content of blood serum samples collected from cattle that are interesting from medical reasons was determined. The results obtained in pathological animals are compared with the normal data and with literature data for similar samples obtained from healthy cattle. Blood samples are collected from jugular zone of 30 cattle. Each serum sample was divided into three samples in order to make analyses by three methods (PIXE, Inductively Coupled Plasma and spectrometry using Bessey-Lowry method). (authors)

  2. Trace elements in human milk

    Energy Technology Data Exchange (ETDEWEB)

    Parr, R M [International Atomic Energy Agency, Vienna (Austria). Div. of Life Sciences

    1983-06-01

    Trace elements are those elements having a concentration lower than 10 ppm in body fluids or tissues. A total of 24 elements, both trace and minor elements, present in human milk have been analysed in this study, employing neutron activation analysis and absorption spectroscopy. The analyses have been carried out collaboratively by several different laboratories and the Agency which has also served as a coordinating centre. Although the evaluation of the results, altogether 8500 separate values, is still in progress, enough evidence is already available, however, to show some very interesting differences between different study areas and, in some cases, between different socio-economic groups within a single country. The main value of these data will probably be to throw new light on the nutritional requirements of young babies for trace elements.

  3. Trace Elements in Human Tooth Enamel

    Energy Technology Data Exchange (ETDEWEB)

    Nixon, G. S. [Turner Dental School, University Of Manchester, Manchester (United Kingdom); Smith, H.; Livingston, H. D. [Department of Forensic Medicine, University Of Glasgow, Glasgow (United Kingdom)

    1967-10-15

    The trace elements are considered to play a role in the resistance of teeth to dental caries. The exact mechanism by which they act has not yet been fully established. Estimations of trace elements have been undertaken in sound human teeth. By means of activation analysis it has been possible to determine trace element concentrations in different layers of enamel in the same tooth. The concentrations of the following elements have been determined: arsenic, antimony, copper, zinc, manganese, mercury, molybdenum and vanadium. The distribution of trace elements in enamel varies from those with a narrow range, such as manganese, to those with a broad range, such as antimony. The elements present in the broad range are considered to be non-essential and their presence is thought to result from a chance incorporation into the enamel. Those in the narrow range appear to be essential trace elements and are present in amounts which do not vary unduly from other body tissues. Only manganese and zinc were found in higher concentrations in the surface layer of enamel compared with the inner layers. The importance of the concentration of trace elements on this surface layer of enamel is emphasized as this layer is the site of the first attack by the carious process. (author)

  4. Determination of trace amounts of rare earth elements in various environmental samples by spark source mass spectrography

    International Nuclear Information System (INIS)

    Sugimae, Akiyoshi

    1978-01-01

    A chemical concentration-mass spectrographic procedure was described for the determination of trace amounts of rare earth elements in various environmental samples: airborne particulate matter, dustfall, soil and so forth. A 0.5 to 1 gram of sample material was decomposed by fusion with sodium carbonate. The silica dehydrated in the usual way was filtered off and the filtrate from the silica was then treated with ammonium hydroxide to precipitate the rare earth elements. After ignition of the precipitate, two ml of internal standard solution containing 20 μg/ml of silver were added and the mixture was then evaporated to dryness. The residue was mixed with an equal amount of graphite powder and then pressed into electrodes. Relative sensitivity coefficients (Ag=1.0) were determined by using Spex Mix and U. S. Geological Survey rock standard G-2. U. S. Geological Survey rock standard GSP-1 and N.B.S. coal fly ash SRM 1633 were analysed to evaluate the accuracy of the proposed method. Comparison of the mass spectral values with literature ones indicated a good agreement. The coefficient of variation obtained by replicate analysis of SRM 1633 was better than 25%. The proposed method was applied to the determination of rare earth elements in airborne particulate matter and dustfall collected on polystyrene filter and in dustjars, respectively. Results for the rare earth elements in the blank of glass fiber filter which was widely used for the collection of airborne particulate matter were also presented. (auth.)

  5. Trace element emissions from coal

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2012-09-15

    Trace elements are emitted during coal combustion. The quantity, in general, depends on the physical and chemical properties of the element itself, the concentration of the element in the coal, the combustion conditions and the type of particulate control device used, and its collection efficiency as a function of particle size. Some trace elements become concentrated in certain particle streams following combustion such as bottom ash, fly ash, and flue gas particulate matter, while others do not. Various classification schemes have been developed to describe this partitioning behaviour. These classification schemes generally distinguish between: Class 1: elements that are approximately equally concentrated in the fly ash and bottom ash, or show little or no fine particle enrichment, examples include Mn, Be, Co and Cr; Class 2: elements that are enriched in the fly ash relative to bottom ash, or show increasing enrichment with decreasing particle size, examples include As, Cd, Pb and Sb; Class 3: elements which are emitted in the gas phase (primarily Hg (not discussed in this review), and in some cases, Se). Control of class 1 trace elements is directly related to control of total particulate matter emissions, while control of the class 2 elements depends on collection of fine particulates. Due to the variability in particulate control device efficiencies, emission rates of these elements can vary substantially. The volatility of class 3 elements means that particulate controls have only a limited impact on the emissions of these elements.

  6. Determination of trace and minor elements in Mexican cigarette wrapping paper

    International Nuclear Information System (INIS)

    Iskander, F.Y.; Manzanares-Acuna, E.

    1999-01-01

    The concentration of 14 elements in cigarette wrapping papers used in manufacturing 21 different Mexican cigarette brands was measured using instrumental thermal neutron activation analysis. These elements are As, Ba, Ce, Co, Cr, Cs, Fe, K, Na, Rb, Sb, Sc, Sr, Th and Zn. The concentration of the elements was compared with the reported concentration in similar studies for elemental content in Pakistani, American, Chinese, Egyptian, Jordanian and Iranian cigarette wrapping papers. (author)

  7. Determination of the levels of trace elements in ten years old children from Antofagasta city, Chile by neutron activation analysis

    International Nuclear Information System (INIS)

    Gras, N.; Munoz, A.L.; Jamett J, A.; Pena C, L.; Santander M, M.

    1988-01-01

    The levels of trace elements in scalp hair of ten years old children of Antofagasta city were determined. For this study, the city was divided in convenient areas. Comparisons between levels of concentrations considering residential areas, sex, values obtained for children of Santiago, and the ranges given in the literature were established. Fifty samples of hair were analyzed by instrumental neutron activation analisis. The elements selected were: As, Br, Co, Cr, Cu, Fe, Hg, K, Na. Sb, and Zn. The effectiveness of wash procedure before irradiation was studied. Ten samples were taken with sufficient amount of hair and each was divided into two, only one of them was washed and both were analyzed. The levels of concentrations were compared. (author)

  8. Determination of lead element trace in some Syrian cigarettes and Its mixtures using voltammetric method on HMDE

    International Nuclear Information System (INIS)

    Nasser, H.; Kabass, H.

    2010-01-01

    This study aims for estimating of trace for these elements in various brands of Syrian Cigarettes and its mixtures, by using voltammetric method (HMDE) hanging mercury drop elec trod. This method is first used to determined Syrian Cigarettes brand and its mixtures, during this study it was found that we can use it easily with low commission, high sensitivity and accurate results comparing with others studies. We prepare the samples by using reference methods. The samples were collected during two times in one year from the same kinds of samples. We noticed that the high concentrations was (3.795μg/g) in Gitanes samples, and the low concentrations in shame samples was (0.37 μg/g). This study refers that there is different concentrations of lead element in this samples.(author)

  9. Determination of Trace Elements in Uranium by HPLC-ID-ICP-MS: NTNFC Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Manard, Benjamin Thomas [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Wylie, Ernest Miller II [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Xu, Ning [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Tandon, Lav [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2017-10-19

    This report covers the FY 16 effort for the HPLC-ID-ICP-MS methodology 1) sub-method validation for the group I&II elements, 2) sub-method stood-up and validation for REE, 3) sub-method development for the transition element, and 4) completion of a comprehensive SOP for three families of elements.

  10. Adaptation of atomic spectrometric methods for the determination of trace elements in whole blood and blood fractions

    International Nuclear Information System (INIS)

    Prohaska, C.

    2002-05-01

    Analytical methods were developed and optimized for the determination of the elements Ca, Cr, Cu, Fe, Mg, Mn, Se, V and Zn in whole blood and in the blood fractions plasma, erythrocytes and lymphocytes of a group of people suffering from diabetes and of a control group of healthy individuals. Cr, Mn, Se and V were analyzed by ETAAS. Ca, Cu, Fe, Mg and Zn were analyzed by ICP-OES. The status of trace elements in lymphocytes of people suffering from diabetes is changed. Physiologically interesting correlations were observed between the clinical parameters cholesterol, HDL, LDL, blood glucose, HbA1c, age and BMI and the trace element concentrations, e.g. a correlation of blood glucose and HbA1c with selenium in whole blood. An ETAAS - method for the determination of Co and Mo was developed and optimized. The samples were digested applying a mixture of HNO3 and HF, different types of graphite furnaces were tested and a multiple injection technique was applied, thereby enabling a contribution to the normal values of these elements in human whole blood. An on-line coupling of a LC, controlled by FIA, with an ICP-OES was developed to investigate the concentrations of the iron species Fe(II) and Fe(III) and the copper species Cu(I) and Cu(II) in human blood plasma. The ICP-OES instrument was adapted, batch experiments were carried out, oxidizing and reducing agents were added and the acidity of the eluens, the flow rate and the integration time were optimized. Choosing alanine for complexation of the species of interest enables their separation under physiological conditions. In the real plasma samples measured most of the copper and iron was found in their oxidized forms. (author)

  11. Determination of trace elements in uranium and aluminum by emission spectrographic methods

    Energy Technology Data Exchange (ETDEWEB)

    Chao, C N; Lee, S L; Tsai, H T

    1976-07-01

    Owing to its simplicity and sensitivity, emission spectrographic method is used to analyze the impurities in nuclear grade uranium rod and aluminum tubings for their strict specifications. With higher quantities of impurities, reactor fuel cladding, aluminum flow-tube, is analyzed by a.c. spark, point to plane method which is developed in quality control without damage for large scale samples. D.C. arc method, either carrier-distillation or without carrier, is developed to determine the limited impurities and it is especially good for analyzing irregular shaped samples. Both standard and sample are converted to oxide form and special standards matching sample matrix are not required. One of the requirements of good reactor fuel and sheathing materials is that, non-fission capture of neutrons by impurities should be held to a minimum. Some of the elements such as boron, cadmium, lithium and rare earths have very great absorption power. It has been shown by calculation that some of them should not exist more than a few parts per million or even a fraction of a part per million. Lithium seldom exists in uranium fuel rod and aluminum sheathing material and is not sought after; the determination of boron and cadmium are included in these reports. Among the carrier-distillation methods, mixture of 3 percent gallium oxide--graphite (2:1) carrier is used in uranium determination and 10 percent silver chloride--lithium fluoride (1:1) carrier is adoped in aluminum analysis. Analytical lines, concentration range and precision data are shown.

  12. Trace element measurements with synchrotron radiation

    International Nuclear Information System (INIS)

    Hanson, A.L.; Kraner, H.W.; Jones, K.W.; Gordon, B.M.; Mills, R.E.

    1982-01-01

    Aspects of the application of synchrotron radiation to trace element determinations by x-ray fluorescence have been investigated using beams from the Cornell facility, CHESS. Fluoresced x rays were detected with a Si(Li) detector placed 4 cm from the target at 90 0 to the beam. Thick samples of NBS Standard Reference Materials were used to calibrate trace element sensitivity and estimate minimum detectable limits for this method

  13. Determination of trace elements in tissues of diabetic rats by INAA

    International Nuclear Information System (INIS)

    Tan Mingguang; Wang Yinsong; Qian Yine; Zhang Guilin

    2000-01-01

    By using streptozotocin (STZ) injection to induce model diabetic rats, instrumental neutron activation analysis was applied to analyze elemental; concentrations in liver, kidney and pancreas tissues in diabetes and control rats. Results obtained for As, Br, Ca, Co, Cl, Cu, Fe, Hg, Mg, Mn, Na, Rb, S, Se and Zn in those tissues show that some elemental contents in diabetic group change obviously when compared with those of the controls. The changes of elemental contents and their significance are discussed

  14. Determination of trace elements in GPC fractions of oil-sand asphaltenes by INAA

    International Nuclear Information System (INIS)

    Jacobs, F.S.; Bachelor, F.W.; Filby, R.H.

    1984-01-01

    Asphaltene samples precipitated from Athabasca and Cold Lake oil-sand bitumens were separated into 12 fractions of varying molecular weight by preparative gel permeation chromatography (GPC). Each fraction was then analyzed by analytical GPC and visible spectrometry. Concentrations of As, Ce, Co, Cr, Eu, Ga, Hf, Hg, La, Ni, Sb, Sc, Se, Sm, Tb, Th, U, V, Zn, and Zr in the fractions were determined by neutron activation analysis. Molecular weights of the Athabasca fractions are generally higher than the corresponding Cold Lake fractions. Between 58% and 90% of the metal contents occur in the high molecular weight fractions of both asphaltenes. Except for V and Cr, which show biomodel distributions, all the elements have decreasing concentrations as the molecular weight of the fraction decreases. High molecular weight fractions, constituting about 55% of the whole asphaltenes, contain nonporphyrin bound vanadium compounds. It is estimated that 27% and 31% of V present in Athabasca and Cold Lake asphaltenes respectively occur as porphyrin type compounds, including vanadyl prophyrins released from the asphaltene micelle during the separation and vanadyl porphyrins bearing high-molecular-weight substituents

  15. Evaluation of some procedures relevant to the determination of trace elemental components in biological materials by destructive neutron activation analysis

    International Nuclear Information System (INIS)

    Berry, D.L.

    1979-01-01

    The development of a simplified procedure for the analysis of biological materials by destructive neutron activation analysis (DNAA) is described. The sample manipulations preceding gamma ray assay were investigated as five specific stages of processing: (1) pre-irradiation treatment; (2) sample irradiation; (3) removal of the organic matrix; (4) removal of interfering radioactivities; and (5) concentration and separation of analyte activities. Each stage was evaluated with respect to susceptibility to sample contamination, loss of trace elemental components, and compatibility with other operations in the overall DNAA procedures. A complete DNAA procedure was proposed and evaluated for the analysis of standard bovine liver and blood samples. The DNAA system was effective for the determination of As, Cu, Fe, Hg, Mo, Rb, Sb, Se, and Zn without yield determinations and with a minimum turn-around time of approximately 3 days

  16. Evaluation of some procedures relevant to the determination of trace elemental components in biological materials by destructive neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Berry, D.L.

    1979-01-01

    The development of a simplified procedure for the analysis of biological materials by destructive neutron activation analysis (DNAA) is described. The sample manipulations preceding gamma ray assay were investigated as five specific stages of processing: (1) pre-irradiation treatment; (2) sample irradiation; (3) removal of the organic matrix; (4) removal of interfering radioactivities; and (5) concentration and separation of analyte activities. Each stage was evaluated with respect to susceptibility to sample contamination, loss of trace elemental components, and compatibility with other operations in the overall DNAA procedures. A complete DNAA procedure was proposed and evaluated for the analysis of standard bovine liver and blood samples. The DNAA system was effective for the determination of As, Cu, Fe, Hg, Mo, Rb, Sb, Se, and Zn without yield determinations and with a minimum turn-around time of approximately 3 days.

  17. Determination of Heavy and Toxic Trace Elements in Sediments of Qarun Lake Using Instrumental Neutron Activation Analysis Technique

    International Nuclear Information System (INIS)

    Hamed, A.; Abd EI-Samad, M.; Soliman, N.F.

    2011-01-01

    An investigation of certain heavy and toxic trace elements in 15 sediment samples from different areas at Qarun Lake was performed by a neutron activation technique using the neutron irradiation facilities of the Second Egyptian Research Reactor (ETRR-2). The samples together with two sets of gold foils (one bare and the other covered with cadmium) and two Standard Reference Materials IAEA (Soil-7) were irradiated at the core of the reactor in two capsules for 8520 seconds, another two capsules each has two sets of gold foils (one bare and the other covered with cadmium) are used to determine the neutron fluxes around the sediment samples. The gamma-rays of nuclides from the irradiated samples were carried out by means of a well calibrated high resolution HPGe detection system. The concentrations of product nuclides containing in the irradiated samples were determined from the peak counting-rates of the prominent gamma-ray lines for the corresponding nuclides using Single External Comparator Method (k 0 -Standardization Method) which called k 0 -NAA technique. The neutron flux ratios (f) in the same radiation sites of the sediment samples bottles were calculated as well as the cadmium ratios (R e d). MS Excel work books were constructed and used in our calculation. The total contents of As , Ba , Ca ,Co, Cr ,Cs, Eu ,Hf ,Hg,Na ,Ru ,Sc ,Se ,Sm ,Sn ,Sr ,Th ,Rb ,Zn ,and Zr in these samples were measured. The objectives .of this study were evaluated to identify the variations of concentration of some elements that have an impact on environmental pollutions. The results indicated that the concentrations of toxic trace elements of Ba, Cr, Se, Sn, Hg, Sin and Zn may represent pollutions problem

  18. Determination of trace elements in hair from Tanzanian children. Effect of dietary factors

    International Nuclear Information System (INIS)

    Mohammed, N.K.; Spyrou, N.M.

    2008-01-01

    The objective of this study was to evaluate the concentrations of essential and toxic elements in hair of children in Tanzania in order to assess their nutritional status. 141 samples of hair from boys and girls living in Tanzania were analyzed using instrumental neutron activation analysis (INAA). The mean concentration levels of Zn and Cu were lower whilst those of other elements were in the same range as the hair elemental concentrations reported in the literature. The lower concentrations of Zn might be related to the diet of mainly cereals with low animal proteins consumed by most of the Tanzanian population. (author)

  19. Simultaneous determination of macronutrients, micronutrients and trace elements in mineral fertilizers by inductively coupled plasma optical emission spectrometry

    Science.gov (United States)

    de Oliveira Souza, Sidnei; da Costa, Silvânio Silvério Lopes; Santos, Dayane Melo; dos Santos Pinto, Jéssica; Garcia, Carlos Alexandre Borges; Alves, José do Patrocínio Hora; Araujo, Rennan Geovanny Oliveira

    2014-06-01

    An analytical method for simultaneous determination of macronutrients (Ca, Mg, Na and P), micronutrients (Cu, Fe, Mn and Zn) and trace elements (Al, As, Cd, Pb and V) in mineral fertilizers was optimized. Two-level full factorial design was applied to evaluate the optimal proportions of reagents used in the sample digestion on hot plate. A Doehlert design for two variables was used to evaluate the operating conditions of the inductively coupled plasma optical emission spectrometer in order to accomplish the simultaneous determination of the analyte concentrations. The limits of quantification (LOQs) ranged from 2.0 mg kg- 1 for Mn to 77.3 mg kg- 1 for P. The accuracy and precision of the proposed method were evaluated by analysis of standard reference materials (SRMs) of Western phosphate rock (NIST 694), Florida phosphate rock (NIST 120C) and Trace elements in multi-nutrient fertilizer (NIST 695), considered to be adequate for simultaneous determination. Twenty-one samples of mineral fertilizers collected in Sergipe State, Brazil, were analyzed. For all samples, the As, Ca, Cd and Pb concentrations were below the LOQ values of the analytical method. For As, Cd and Pb the obtained LOQ values were below the maximum limit allowed by the Brazilian Ministry of Agriculture, Livestock and Food Supply (Ministério da Agricultura, Pecuária e Abastecimento - MAPA). The optimized method presented good accuracy and was effectively applied to quantitative simultaneous determination of the analytes in mineral fertilizers by inductively coupled plasma optical emission spectrometry (ICP OES).

  20. Determination of trace elements in poly(methyl methacrylate) by neutron activation analysis

    International Nuclear Information System (INIS)

    Kobayashi, M.

    1979-01-01

    The results are reported of the neutron activation analysis of poly(methyl methacrylate) polymerized with a redox system of chromium (II) acetate and p-chlorobenzyl peroxide in dimethylformamide at 30 0 C. Since the polymer was originally synthesized in experiments for kinetic studies, the results indicate an arbitrary background of purity of polymers obtained in a laboratory. Samples were irradiated for 28m and gamma spectra detected trace amounts of chlorine, aluminum, vanadium, magnesium, manganese, potassium, copper, zinc, sodium, bromine, lanthanum, gold, and chromium. 2 figures, 1 table

  1. [Trace elements of bone tumors].

    Science.gov (United States)

    Kalashnikov, V M; Zaĭchik, V E; Bizer, V A

    1983-01-01

    Due to activation analysis involving the use of neutrons from a nuclear reactor, the concentrations of 11 trace elements: scandium, iron, cobalt, mercury, rubidium, selenium, silver, antimony, chrome, zinc and terbium in intact bone and skeletal tumors were measured. 76 specimens of bioptates and resected material of operations for bone tumors and 10 specimens of normal bone tissue obtained in autopsies of cases of sudden death were examined. The concentrations of trace elements and their dispersion patterns in tumor tissue were found to be significantly higher than those in normal bone tissue. Also, the concentrations of some trace elements in tumor differed significantly from those in normal tissue; moreover, they were found to depend on the type and histogenesis of the neoplasm.

  2. Biological trace element measurements using synchrotron radiation

    International Nuclear Information System (INIS)

    Giauque, R.D.; Jaklevic, J.M.; Thompson, A.C.

    1985-07-01

    The feasibility of performing x-ray fluorescence trace element determinations at concentrations substantially below the ppM level for biological materials is demonstrated. Conditions for achieving optimum sensitivity were ascertained. Results achieved for five standard reference materials were, in most cases, in excellent agreement with listed values. Minimum detectable limits of 20 ppM were measured for most elements

  3. Application of the Total Reflection X-ray Fluorescence technique to trace elements determination in tobacco

    International Nuclear Information System (INIS)

    Martinez, T.; Lartigue, J.; Zarazua, G.; Avila-Perez, P.; Navarrete, M.; Tejeda, S.

    2008-01-01

    Many studies have identified an important number of toxic elements along with organic carcinogen molecules and radioactive isotopes in tobacco. In this work we have analyzed by Total Reflection X-Ray Fluorescence 9 brands of cigarettes being manufactured and distributed in the Mexican market. Two National Institute of Standards and Technology standards and a blank were equally treated at the same time. Results show the presence of some toxic elements such as Pb and Ni. These results are compared with available data for some foreign brands, while their implications for health are discussed. It can be confirmed that the Total Reflection X-Ray Fluorescence method provides precise (reproducible) and accuracy (trueness) data for 15 elements concentration in tobacco samples

  4. Application of the Total Reflection X-ray Fluorescence technique to trace elements determination in tobacco

    Science.gov (United States)

    Martinez, T.; Lartigue, J.; Zarazua, G.; Avila-Perez, P.; Navarrete, M.; Tejeda, S.

    2008-12-01

    Many studies have identified an important number of toxic elements along with organic carcinogen molecules and radioactive isotopes in tobacco. In this work we have analyzed by Total Reflection X-Ray Fluorescence 9 brands of cigarettes being manufactured and distributed in the Mexican market. Two National Institute of Standards and Technology standards and a blank were equally treated at the same time. Results show the presence of some toxic elements such as Pb and Ni. These results are compared with available data for some foreign brands, while their implications for health are discussed. It can be confirmed that the Total Reflection X-Ray Fluorescence method provides precise (reproducible) and accuracy (trueness) data for 15 elements concentration in tobacco samples.

  5. Trace element determination in human bones using the neutron activation analysis method

    International Nuclear Information System (INIS)

    Kramarski, Sila; Saiki, Mitiko; Borelli, Aurelio; Batalha, Joao R.F.

    1997-01-01

    This work presents the results obtained in the analysis of rib bone samples from normal human individuals by applying instrumental neutron activation analysis. In these analyses, the elements Br, Cl, Fe, K, Mg, Na, Rb, Sr and Zn were found at the ppm level and the elements Ca and P at the level of percentage. The precision and the of the results were evaluated by using biological reference materials NIST SRM 1577a Bovine Liver, IAEA A-11 Milk powder, NIES CRM 9 Sargasso e NIES CRM 10A Rice Flour Unpolished. (author). 5 refs., 3 tabs

  6. Simultaneous determination of macronutrients, micronutrients and trace elements in mineral fertilizers by inductively coupled plasma optical emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira Souza, Sidnei de [Laboratório de Química Analítica Ambiental (LQA), Departamento de Química, Centro de Ciências Exatas e Tecnologia, Universidade Federal de Sergipe (UFS), 49100-000, São Cristovão, SE (Brazil); Silvério Lopes da Costa, Silvânio [Laboratório de Química Analítica Ambiental (LQA), Departamento de Química, Centro de Ciências Exatas e Tecnologia, Universidade Federal de Sergipe (UFS), 49100-000, São Cristovão, SE (Brazil); Coordenação de Química, Universidade Federal de Alagoas (UFAL), Campus Arapiraca, 57309-005, Arapiraca, AL (Brazil); Santos, Dayane Melo; Santos Pinto, Jéssica dos; Garcia, Carlos Alexandre Borges [Laboratório de Química Analítica Ambiental (LQA), Departamento de Química, Centro de Ciências Exatas e Tecnologia, Universidade Federal de Sergipe (UFS), 49100-000, São Cristovão, SE (Brazil); and others

    2014-06-01

    An analytical method for simultaneous determination of macronutrients (Ca, Mg, Na and P), micronutrients (Cu, Fe, Mn and Zn) and trace elements (Al, As, Cd, Pb and V) in mineral fertilizers was optimized. Two-level full factorial design was applied to evaluate the optimal proportions of reagents used in the sample digestion on hot plate. A Doehlert design for two variables was used to evaluate the operating conditions of the inductively coupled plasma optical emission spectrometer in order to accomplish the simultaneous determination of the analyte concentrations. The limits of quantification (LOQs) ranged from 2.0 mg kg{sup −1} for Mn to 77.3 mg kg{sup −1} for P. The accuracy and precision of the proposed method were evaluated by analysis of standard reference materials (SRMs) of Western phosphate rock (NIST 694), Florida phosphate rock (NIST 120C) and Trace elements in multi-nutrient fertilizer (NIST 695), considered to be adequate for simultaneous determination. Twenty-one samples of mineral fertilizers collected in Sergipe State, Brazil, were analyzed. For all samples, the As, Ca, Cd and Pb concentrations were below the LOQ values of the analytical method. For As, Cd and Pb the obtained LOQ values were below the maximum limit allowed by the Brazilian Ministry of Agriculture, Livestock and Food Supply (Ministério da Agricultura, Pecuária e Abastecimento — MAPA). The optimized method presented good accuracy and was effectively applied to quantitative simultaneous determination of the analytes in mineral fertilizers by inductively coupled plasma optical emission spectrometry (ICP OES). - Highlights: • Determination of inorganic constituents in mineral fertilizers was proposed. • Experimental design methodology was used to optimize analytical method. • The sample preparation procedure using diluted reagents (HNO{sub 3} and H{sub 2}O{sub 2}) was employed. • The analytical method was satisfactorily to the determination of thirteen elements. • The

  7. Application of spectroscopic Techniques for the determination of trace element concentrations in some Sudanese vegetables and fruits

    International Nuclear Information System (INIS)

    Ahmed, A. N.; Ali, A. H.; Eltayeb, M. A. H.; Osman, M. M.; Taha, K. K.

    2004-12-01

    The objective of this study were to determine the levels of the mineral nutrients, especially of trace elements, in some food items commonly consumed in Sudan and to compare the results of this work with local and international data. To achieve these objectives, food samples analyzed were collected from different localities in Sudan, and the samples were prepared for analysis by using dry ashing and wet digestion. Atomic absorption spectroscopy (AAS), x-ray fluorescence spectroscopy (XRF), flame photometry and colorimetry were used for the determination of the concentrations of elements in the samples, samples were ashed using muffle furnace at temperature 550 C. The quality of the data was verified by the analysis of standard reference materials TDD-ID and Hay-9. The levels of the elemental contents (Br, Ca, Co, Cu, Fe, Mg, Mn, P, Pb, Na, Rb, Sr, and Zn) were determined in legumes, cereals, oil seeds, flour and cereals products, vegetables, fruits, milk and milk products, egg, meats and fish, and oils and fats. The Sudanese food items analyzed were found to contain considerable ranges of nutrients as follows. Concentration levels for some of these elements Ca, Cu and Fe show values which were higher in fruits(4709, 21, and 633 ppm, respectively), and lower in vegetables (4094, 13, and 255 ppm, respectively). Pb and Mn were higher in vegetables (2 and 32 ppm, respectively) and lower in fruits (1 and 18 ppm) respectively). Na and Zn were higher in vegetables (3149 and 26 ppm, respectively) and lower fruits (269 and 13 ppm, respectively). The values obtained agree, in general, with data available from other countries. Variations were observed among certain varieties of food.(Author)

  8. Application of spectroscopic techniques of analysis for the determination of trace elements concentrations in some sudanese food items

    International Nuclear Information System (INIS)

    Ahmed, A. N.; Ali, A.H.; Eltayeb, M. A.; Ahmed, M.M.O

    2004-01-01

    The objectives of this study were to determine the levels of the mineral nutrients, especially of trace elements, in some food items commonly consumed in sudan and to compare the results of this work with local and inter nation data. to achieve these objectives.Food samples were collected from different localities in sudan, and the samples were prepared for analysis using dry ashing and wet digestion. Atomic absorption spectroscopy (Aas), X-ray florescence spectroscopy (XRF), flame photometry and colorimetry were used for the determination of the concentrations of elements in the samples. Samples were ashed using muffle furnace at temperature 55 degree C. The quality of the data was verified by the analysis of standard reference materials TDD-Id and hay-9. The levels of the elemental contents (Br,Ca,Co,Cu,Fe,Mg,Mn,P,Pb,Na,Rb,Sr, and Zn) were determined in legumes, cereals, oil seeds, flour and cereal products, vegetables, fruits, milk and milk products, egg, meats and fish, and oils and fats. The sudanese food items analyzed were found to contain considerable ranges of nutrients as follows:-concentration levels for some of these elements Ca, Cu and Fe show values which were higher in fruits (4709,21, and 633 ppm, respectively), and lower in oils and fat s (25, 2, and 11 ppm, respectively). Pb and Mn were higher in flour and cereals products (4 and 34 ppm, respectively) and lower in fruits (1 ppm) and meats and fish (1 ppm and 4 ppm, respectively ). Na and Zn were higher in flour and cereals products and legumes (4970 and 39 ppm, respectively). The values obtained agree, in general, with data available from other countries. Variations were observed among certain varieties of food. (Author)

  9. Determination of trace element level in different tissues of the leaping mullet (Liza saliens, Mugilidae) collected from Caspian Sea.

    Science.gov (United States)

    Ebrahimzadeh, Mohammad Ali; Eslami, Shahram; Nabavi, Seyed Fazel; Nabavi, Seyed Mohammad

    2011-12-01

    The concentrations of Cr, Cu, Fe, Mn, Ni, Pb, Cd, and Zn were determined in the brain, heart, liver, gill, gonad, spleen, kidney, and red and white muscles of Liza saliens (leaping mullet). Trace element levels in fish samples were analyzed by flame atomic absorption spectrometry. Among the non-essential metals, the levels of Ni and Pb in the tissues were higher than limits for fish proposed by FAO/WHO, EU, and TFC. Generally, the levels of the non-essential metals were much higher than those of manganese in the red and white muscles. Fe distribution pattern in tissues was in order of spleen > liver > heart > gill > brain > kidney > gonad > red muscle > white muscle. Red muscle was not within the safe limits for human consumption because non-essential metal (Ni, Pb) contents were higher than standard limits.

  10. Multielement determination of trace elements in seawater by inductively coupled plasma mass spectrometry after tandem preconcentration with cooperation of chelating resin adsorption and lanthanum coprecipitation

    International Nuclear Information System (INIS)

    Yabutani, Tomoki; Chiba, Koichi; Haraguchi, Hiroki

    2001-01-01

    A tandem preconcentration method, in which chelating resin adsorption and La coprecipitation were cooperatively employed for preconcentration, was developed as a pretreatment method for simultaneous multielement determination of trace elements in seawater by ICP-MS. First, the seawater sample (250 ml) was treated with a chelating resin for preconcentration of trace elements, and then trace elements with good recoveries were determined by ICP-MS. Trace elements with the chemical properties of oxoanion- and hydride-formation, which were poorly recovered in the chelating resin preconcentration, were further subjected to preconcentration by La coprecipitation. As a result, more than 30 elements could be determined in the concentration range from 9.6 μg L -1 for Mo to 0.00018 μg L -1 for Tm, when the present tandem method was applied to the analysis of open seawater standard reference material (NASS-4). Furthermore, the analytical results for open seawater reference materials were compared with those for coastal seawater reference material as well as for coastal seawater collected in the Ise Bay. It was found that the multielement data for trace elements in these seawater samples clearly showed different elemental distributions, reflecting the different marine environments. (author)

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

    International Nuclear Information System (INIS)

    Sanchez P, L.A.; Benavides M, A.M.

    1996-01-01

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

  12. Trace elements in brazilian soils

    International Nuclear Information System (INIS)

    Rocha, Geraldo Cesar

    1995-01-01

    A literature revision on trace elements (Zn, B, Mn, Mo, Cu, Fe, and Cl) in Brazilian soils was prepared, with special attention to the chemical form and range in the soil, extraction methods and correlation of the amount in soils with soil properties

  13. Background levels of some trace elements in egyptian soils determined by neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Abdel-Sabour, M F [Soil pollution unit, Soil and water dept., Nuclear res.center, Cairo (Egypt); Abdel-Haleen, A S [Hot Labs, Atomic Energy Authority, Cairo (Egypt); Zohny, E E [Physics Dept. Faculty of Science, Cairo Univ. Ain shams Univ., Cairo, (Egypt); Sroor, A [Nuclear Physics Dep., Faculty of Girls, Ain Shams Univ., Cairo (Egypt); Zaghloul, R [Mubarak city for scientific research and technology, Ministry of scientific research, Cairo, (Egypt)

    1997-12-31

    As part of a research program on the influence of agricultural practices and activities on soil content of heavy metals. The present work was carried out to investigate the feasibility of instrumental neutron activation analysis for this purpose. Elements studied were, Fe, Zn, Co, Sc, Sb, As, Cd, Hg and Cr. The soil samples analyzed were from different locations to represent different land uses and types. Results revealed that As, Cd and Hg show a pronounced accumulation in soils especially those exposed to industrial and organic wastes disposal. 2 tabs.

  14. Application of Spectroscopic Techniques for the Determination of Trace Element Concentrations in some Sudanese vegetables and fruits

    International Nuclear Information System (INIS)

    Ahmed, A. N.; Ali, A. H.; Eltayeb, M. A. H.; Othman, M. M.; Taha, K. K.

    2004-01-01

    The objectives of this study were to determine the levels of the mineral nutrients, especially of trace elements, in some food items commonly consumed in Sudan and to compare the results of this work with local and international data. Food samples of fruits and vegetables were collected from different localities in Sudan. The samples were then prepared and their Br, Ca, Co, Cu, Fe, Mg, Mn, P, Pb, Na, Rb, Sr, and Zn content were determined using Atomic absorption spectroscopy (AAS), X-ray fluorescence spectroscopy (XRF), flame photometry and colorimetry. Verified standards TDD-1D and Hay-9 (supplied by the IAEA) were measured using the techniques mentioned above for accuracy. The Sudanese food items analyzed were found to contain considerable ranges of nutrients as follows: - Concentration levels for some of these elements Ca, Cu and Fe show higher values in fruits (4709, 21, and 633 ppm, respectively), and lower in vegetables (4094, 13, and 255 ppm , respectively). Pb and Mn were higher in vegetables (2 and 32 ppm, respectively) and lower in fruits (1 and 18 ppm) respectively). Na and Zn were higher in vegetables (3149 and 26 ppm, respectively) and lower in fruits (269 and 13 ppm, respectively). The values obtained agree, in general, with data available from other countries. Variations were observed among certain varieties of food. (Authors)

  15. Determination of trace elements in soy milk using ICP atomic emission spectrometry

    International Nuclear Information System (INIS)

    Tanaka, Satoko; Chayama, Kenji

    2009-01-01

    The present study investigated the optimal method for the multi-element quantification of 9 elements in soy milk: calcium, copper, iron, potassium, magnesium, manganese, sodium, phosphorus, and zinc. Results obtained using ICP atomic emission spectrometry were compared with those obtained by atomic absorption spectrometry, which is the standard method. The same sample was measured using both ICP atomic emission spectrometry and atomic absorption spectrometry. The percentage of minerals recovered by ICP atomic emission spectrometry ranged from 99.3% to 102%, which was equivalent to that by atomic absorption spectrometry. Therefore, a good result with standard deviation was obtained. The mineral contents of 16 samples of commercially-available soy milk products were measured. The Cu content was significantly proportional to the amount of soybean solids (P < 0.001). Moreover, although relation-ships did not attain statistical significance, the consents of Fe, Zn, K, Mg and P were proportional to the amount of soybean solids, and were highest in soy milk, followed by prepared soy milk and so milk beverage. The Ca content of modified soy milk was significantly higher than that of soy milk and soy milk-based beverages (P < 0.001). Furthermore, the Na content in soy milk was significantly lower. (author)

  16. Report on intercomparison air-3/1 of the determination of trace elements in simulated air filters

    International Nuclear Information System (INIS)

    Pszonicki, L.; Veglia, A.; Suschny, O.

    1982-06-01

    The report is a sum up of an intercomparison experiment organized by the Analytical Quality Control Service of the IAEA, for simulated air filters (Air-3/1) spiked with 17 trace elements. The purpose was twofold: to assist participating laboratories in controlling their own performance, and to characterize exactly the prepared batch of air filters in order to be able to use them as reference filters for elemental trace analysis. The results submitted by 29 laboratories from 20 countries are presented and statistically processed. The analytical methods used are also specified. Conclusions concerning the use of filters Air-3/1 as certified reference filters are presented

  17. Minor and trace elements in melanins determined by neutron activation analysis

    International Nuclear Information System (INIS)

    Kochanska-Dziurowicz, A.A.; Wilczok, T.; Mosulishvili, L.; Kharabadze, N.

    1986-01-01

    The presence of Au, Br, Sb, Ag, Fe, Zn, Co, Cr, Ni, Hg and Sn determined by neutron activation analysis was demonstrated in melanins isolated from human dark hair, banana peels or prepared synthetically from tyrosine. (author)

  18. Determination of trace cadmium and other elements in bone by epithermal neutron activation analysis

    International Nuclear Information System (INIS)

    Dowlati, R.; Jervis, R.E.

    1991-01-01

    Epithermal neutron activation analysis (ENAA) was applied to measure quantitatively Cd and other elements in bone samples from control and Cd-fed rats. This method was found to be non-destructive to the bone samples, with no sign of 'radiolytic charring' and was sensitive enough to detect and quantify Cd in bone samples at normal levels for mammals (viz. 0.5-1.0μg/g) and higher. Two different thermal neutron shield materials were utilized, namely cadmium and boron. The boron shield resulted in a 27% improvement in the detection limit of Cd in bone. The accuracy of ENAA for Cd was assessed by intercomparison with electrothermal atomic absorption spectrophotometry (ETAAS), and the results were in fair agreement (±23%) with those from ENAA. (author) 24 refs.; 5 tabs

  19. Application of neutron activation analysis to biological materials. Pt. 4. Approach to simultaneous determination of trace elements in human eye tissues with non-destructive neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Yamaguchi, T; Bando, M; Nakajima, A [Juntendo Univ., Tokyo (Japan). School of Medicine; Terai, M [Tokyo Metropolitan Univ. (Japan). Faculty of Science; Suzuki-Yasumoto, M [National Inst. of Radiological Sciences, Chiba (Japan)

    1980-01-01

    Fourteen trace elements (short-lived nuclides: Al, Br, Cu, Mn and V; long-lived nuclides: Ag, Au, Cd, Co, Cr, Fe, Sc, Se and Zn) in human eye tissues are determined simultaneously by non-destructive neutron activation analysis. The quantity of Al, Br, Fe, Se and Zn in the eye tissues (about 1 to more than 10 ..mu..g/g dry weight tissue) seems to be higher than that of other trace elements, although the content of each trace element in individual tissue is scattered in a wide range. Conjunctiva, iris (+ciliary body) and choroid (+pigment epithelium) seem to contain larger amount of various trace elements than other eye tissues. From correlation studies it is evident that the relative distribution of 14 trace elements in various eye tissues are similar, and furthermore the content of trace elements in the eye tissues may be correlated in each of the three groups (group A: Cd, Se and Zn; group B: Al, Cr, Fe, Se and V; group C: Al, Au, Fe and Se).

  20. Determination of trace elements in fish by instrumental neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Awadallah, R.M.; Mohamed, A.E.; Gabr, S.A.

    1985-08-01

    INAA was utilized for the determination of Al, Au, Br, Ca, Cl, Co, Cr, Cu, Fe, I, K, Mg, Mn, Na, Rb, Sc, V and W in 12 Tilapia Nilotica samples collected from the Aswan High Dam Lake following destructive techniques. The results are tabulated.

  1. Trace elements in 11 fruits widely-consumed in the USA as determined by neutron activation analysis

    International Nuclear Information System (INIS)

    Michenaud-Rague, A.; Robinson, S.; Landsberger, S.

    2012-01-01

    While there is a lot of information on the elemental content of food for nutritional and pollution studies, the analysis of fruits has received little attention. We have investigated 11 commonly eaten fruits for their trace and minor element constituents by neutron activations including thermal and epithermal neutron activation analysis. Our results revealed that both blueberries and strawberries had the most of top two highest elemental concentrations followed by raspberries, oranges and mango. Bananas, grapes, plums, apples, pears, and cherries had the fewest or none of the most elevated elemental concentrations. (author)

  2. Cell-selective determination of trace elements in testis by SR-XRF analysis with nanoprobe

    International Nuclear Information System (INIS)

    Homma-Takeda, Shino; Nishimura, Yoshikazu; Watanabe, Yoshito; Yukawa, Masae; Ueno, Shunji; Terada, Yasuko

    2005-01-01

    Organotin compounds are widely used in industry and its environmental contamination by these compounds has recently become a concern. It is known that they act as endocrine disruptors but details of the dynamics of Sn in reproductive organs are still unknown. In the present study, we attempted to determine Sn in the testis of rats exposed to tributyltin chloride (TBTC) cell-selectively by synchrotron radiation X-ray florescence analysis with nanoprobe. TBTC was orally administered to rats at a dose of 45 μmol/kg per day for 3 days. One day later, Sn was detected in spermatozoa at the stage VIII seminiferous tubule, which are the final step of spermatogenesis in the testis. Sn levels in the microdissectioned seminiferous tubules determined by inductively coupled argon plasma-mass spectrometry were approximately equivalent to that in the testis. These data indicate that Sn accumulates in germ cells as well as in spermatozoa in a short period of TBTC exposure. (author)

  3. Determination of trace element levels in leaves of Nerium oleander using X-Ray Fluorescence

    International Nuclear Information System (INIS)

    Santos, Ramon S.; Sanches, Francis A.C.R.A.; Neves, Arthur O.P.; Oliveira, Luis F.; Oliveira, Davi F.; Anjos, Marcelino J.

    2013-01-01

    The environmental pollution by human activity has been one of the most concerns in the last years, principally due to rapid urban growth in the cities and the industrialization process. The air pollution can be increased due to several different kinds of emissions: urban traffic, industrial activities, burning fuel, civil industry of construction/demolition, fires and natural phenomena. Many of these emissions move from long distances due to convections currents and finally tend to deposit mainly in the plants leaves and in the soil. Thus, the plants leaves works as a natural sampler by the emissions deposit in these ones. In this study Nerium oleander leaves were used to measure the environmental pollutions levels in different sampling urban regions in the city of Rio de Janeiro/RJ: Andarai, Benfica, Bonsucesso, Caju, Engenho de Dentro, Engenho Novo, Estacio, Grajau, Inhauma, Lins, Maracana, Maria da Graca, Meier, Praca da Bandeira, Riachuelo, Rio Comprido, Sao Cristovao, Tijuca, Vila Isabel and city Center. The control samples were collected in Campo Grande near of Parque Nacional da Pedra Branca/RJ (National Park of Pedra Branca/RJ). The leaves were collected from adult plants and after the collection the samples were cleaned and placed in the greenhouse for drying, then were mashed and pressed into tablets forms. The analyses were performed using the energy dispersion X-ray fluorescence (EDXRF), developed on the own laboratory and based in a SiPIN detector and a mini X ray tube. It was possible to detect 16 elements in the analyzed samples: K, Ca, Cr, Mn, Fe, Cu, Zn, Br, Rb, Sr, Ba and Pb. The results shows that, in the studied areas, the analysis of the Nerium oleander plant shows a low-cost option and with a substantial efficiency as an environmental pollution biomonitor. (author)

  4. Determination of trace element levels in leaves of Nerium oleander using X-Ray Fluorescence

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Ramon S.; Sanches, Francis A.C.R.A.; Neves, Arthur O.P.; Oliveira, Luis F.; Oliveira, Davi F.; Anjos, Marcelino J. [Universidade do Estado do Rio de Janeiro (UERJ), Rio de Janeiro, RJ (Brazil). Inst. de Fisica Armando Dias Tavares. Dept. de Fisica Aplicada e Termodinamica

    2013-07-01

    The environmental pollution by human activity has been one of the most concerns in the last years, principally due to rapid urban growth in the cities and the industrialization process. The air pollution can be increased due to several different kinds of emissions: urban traffic, industrial activities, burning fuel, civil industry of construction/demolition, fires and natural phenomena. Many of these emissions move from long distances due to convections currents and finally tend to deposit mainly in the plants leaves and in the soil. Thus, the plants leaves works as a natural sampler by the emissions deposit in these ones. In this study Nerium oleander leaves were used to measure the environmental pollutions levels in different sampling urban regions in the city of Rio de Janeiro/RJ: Andarai, Benfica, Bonsucesso, Caju, Engenho de Dentro, Engenho Novo, Estacio, Grajau, Inhauma, Lins, Maracana, Maria da Graca, Meier, Praca da Bandeira, Riachuelo, Rio Comprido, Sao Cristovao, Tijuca, Vila Isabel and city Center. The control samples were collected in Campo Grande near of Parque Nacional da Pedra Branca/RJ (National Park of Pedra Branca/RJ). The leaves were collected from adult plants and after the collection the samples were cleaned and placed in the greenhouse for drying, then were mashed and pressed into tablets forms. The analyses were performed using the energy dispersion X-ray fluorescence (EDXRF), developed on the own laboratory and based in a SiPIN detector and a mini X ray tube. It was possible to detect 16 elements in the analyzed samples: K, Ca, Cr, Mn, Fe, Cu, Zn, Br, Rb, Sr, Ba and Pb. The results shows that, in the studied areas, the analysis of the Nerium oleander plant shows a low-cost option and with a substantial efficiency as an environmental pollution biomonitor. (author)

  5. Worldwide Open Proficiency Test for X ray Fluorescence Laboratories PTXRFIAEA08: Determination of Minor and Trace Elements in Natural Soil

    International Nuclear Information System (INIS)

    2014-01-01

    The IAEA assists Member State laboratories to maintain their readiness by producing reference materials, developing standardized analytical methods, and conducting interlaboratory comparisons and proficiency tests as tools for quality control. To ensure a reliable, worldwide, rapid and consistent response, the IAEA Nuclear Spectrometry and Applications Laboratory organizes tests for Member State laboratories. This publication presents the results of the worldwide proficiency test PTXRFIAEA08 on the determination of minor and trace elements in natural soil. Methodologies, a data evaluation approach, a summary evaluation of each element and individual evaluation reports for each laboratory are also described. The test was carried out within the IAEA project Nuclear Spectrometry for Analytical Applications, under the Nuclear Science Programme. The main objective of the project was to enhance the capability of interested Member States in effective utilization of nuclear spectrometries and analytical services in industry, human health and agriculture, and in monitoring and evaluating environmental pollution. This proficiency test was designed to identify analytical problems and to support Member State laboratories in improving the quality of their analytical results, maintaining their accreditation and providing a regular forum for discussion and technology transfer in this area. The type of sample and the concentration levels of the analytes were designed to enable the identification of potential analytical problems

  6. Worldwide Open Proficiency Test for X Ray Fluorescence Laboratories PTXRFIAEA/06: Determination of Minor and Trace Elements in Grass Mixture

    International Nuclear Information System (INIS)

    2011-01-01

    The IAEA assists its Member States laboratories to maintain their readiness by producing reference materials, by developing standardized analytical methods, and by conducting interlaboratory comparisons and proficiency tests as tools for quality control. To ensure a reliable worldwide, rapid and consistent response, the IAEA Nuclear Spectrometry and Applications Laboratory in Seibersdorf, Austria organises tests. This summary report presents the results of the worldwide proficiency test IAEA-PTXRF-06 on the determination of minor and trace elements in a grass mixture. Methodologies, data evaluation approach, summary evaluation of each element and individual evaluation reports for each laboratory are also described. The test was carried out under IAEA Project 1.4.3.4 (D.3.03), Nuclear Spectrometry for Analytical Applications, under the Nuclear Science Programme. The main objective of this project is to enhance the capability of interested Member States in effective utilization of nuclear spectrometries and analytical services in industry, human health, agriculture, and in monitoring and evaluation of environmental pollution. This proficiency test was designed to identify analytical problems, to support IAEA Member States laboratories to improve the quality of their analytical results, to maintain their accreditation and to provide a regular forum for discussion and technology transfer in this area. The type of sample and the concentration levels of the analytes were designed in a way to enable identification of potential analytical problems. The next proficiency test exercise is expected to be organized in 2010

  7. World-wide and regional intercomparison for the determination of trace elements in tuna fish homogenate sample IAEA-350

    Energy Technology Data Exchange (ETDEWEB)

    Mee, L D; Oregioni, B; Horvat, M [International Atomic Energy Agency, Marine Environment Laboratory, Monaco (Monaco)

    1992-12-01

    The accurate and precise determination of trace elements in marine biological samples is an important aspect of marine pollution studies, especially regarding studies of human exposure to toxic elements through sea food consumption. Past intercomparison studies conducted by the Marine Environment Laboratory of IAEA (formerly the International Laboratory of Marine Radioactivity) have focused upon various marine organisms including fish, bivalves and crustaceans. The present intercalibration exercise was designed in order to satisfy the increased demand for certified reference materials of various origins and the wide range of parameters that should be studied. Additionally, different instrumental techniques, both nuclear and non-nuclear, were compared, and evaluated. By statistically examining the data from this study, the material can be certified for future use as a reference material. The present report presents the entire experimental data set ana a statistical evaluation of the results for each parameter. It should enable individual participants to assess their performance and make appropriate modifications to their laboratory's analytical procedures where necessary. Additionally, a graphical evaluation is made of the data for parameters where a consensus value could not easily be achieved in order to examine the source of any systematic errors. The exercise was designed to satisfy the requirements of participants in IAEA's Analytical Quality Assurance Service as well as laboratories involved in UNEP's Regional Seas Programme and similar activities conducted within the auspices of GIPME (Global Investigations of Pollution in the Marine Environment)

  8. A multi-element solid-phase extraction method for trace metals determination in environmental samples on Amberlite XAD-2000

    International Nuclear Information System (INIS)

    Bulut, Volkan Numan; Gundogdu, Ali; Duran, Celal; Senturk, Hasan Basri; Soylak, Mustafa; Elci, Latif; Tufekci, Mehmet

    2007-01-01

    A method for the preconcentration of some transition elements at trace level was proposed using a column filled with Amberlite XAD-2000 resin. Metal ions were adsorbed on XAD-2000 as their diethyldithiocarbamate chelates, then analytes retained on the resin were eluted by 1 mol L -1 nitric acid in acetone and determined by flame atomic absorption spectrometry (FAAS). The influences of some analytical parameters including pH of sample solution, ligand amount, the type, concentration and volume of elution solution, flow rates of the sample and eluent solutions, adsorption capacity of the resin and sample volume on the preconcentration efficiency have been investigated. The influences of some matrix elements were also examined. The detection limit (N = 20, 3 sigma) for Mn(II), Fe(II), Co(II), Cu(II), Cd(II), Zn(II), Pb(II) and Ni(II) were found as 0.20, 0.35, 0.25, 0.20, 0.20, 0.15, 0.45 and 0.25 μg L -1 , respectively. The validation of the procedure was carried out by analysis of certified reference materials. The proposed method was applied to natural waters and kale vegetable (Brassica oleracea var. acephala)

  9. A multi-element solid-phase extraction method for trace metals determination in environmental samples on Amberlite XAD-2000

    Energy Technology Data Exchange (ETDEWEB)

    Bulut, Volkan Numan [Department of Chemistry, Giresun Faculty of Arts and Sciences, Karadeniz Technical University, 28049 Giresun (Turkey); Gundogdu, Ali [Department of Chemistry, Faculty of Arts and Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey); Duran, Celal [Department of Chemistry, Faculty of Arts and Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey); Senturk, Hasan Basri [Department of Chemistry, Faculty of Arts and Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey); Soylak, Mustafa [Department of Chemistry, Faculty of Arts and Sciences, Erciyes University, 38039 Kayseri (Turkey)]. E-mail: msoylak@gmail.com; Elci, Latif [Department of Chemistry, Faculty of Arts and Sciences, Pamukkale University, 20020 Denizli (Turkey); Tufekci, Mehmet [Department of Chemistry, Faculty of Arts and Sciences, Karadeniz Technical University, 61080 Trabzon (Turkey)

    2007-07-19

    A method for the preconcentration of some transition elements at trace level was proposed using a column filled with Amberlite XAD-2000 resin. Metal ions were adsorbed on XAD-2000 as their diethyldithiocarbamate chelates, then analytes retained on the resin were eluted by 1 mol L{sup -1} nitric acid in acetone and determined by flame atomic absorption spectrometry (FAAS). The influences of some analytical parameters including pH of sample solution, ligand amount, the type, concentration and volume of elution solution, flow rates of the sample and eluent solutions, adsorption capacity of the resin and sample volume on the preconcentration efficiency have been investigated. The influences of some matrix elements were also examined. The detection limit (N = 20, 3 sigma) for Mn(II), Fe(II), Co(II), Cu(II), Cd(II), Zn(II), Pb(II) and Ni(II) were found as 0.20, 0.35, 0.25, 0.20, 0.20, 0.15, 0.45 and 0.25 {mu}g L{sup -1}, respectively. The validation of the procedure was carried out by analysis of certified reference materials. The proposed method was applied to natural waters and kale vegetable (Brassica oleracea var. acephala)

  10. Determination of trace elements of Egyptian crops by neutron activation analysis. Pt. 3. Trace elements in African tea, ginger, canella bark, black pepper, sesame, lady's fingers, jew's mallow, tomatos, cucumber and marrow

    Energy Technology Data Exchange (ETDEWEB)

    Sherif, M K; Awadallah, R M; Amrallah, A H [Assiut Univ. (Egypt)

    1980-01-01

    Multielemental neutron activation analysis was used for the determination of Al, As, Au, Br, Ca, Cd, Co, Cr, Cu, Fe, La, Mn, Mo, Sb, Se, W and Zn in African tea and lady's fingers (Malvaceae Family), ginger (Zingiperanceae Family), canella bark (Laureceae Family), black pepper (Piperaceae Family), cucumber seeds and vegetable marrow seeds (Cucurbitaceae Family), tomatos seed (Solanaceae Family), safflower seeds (Compositae Family), jew's mallow seed (Tiliaceae Family) and sesame (Pedaliaceae Family). Trace elements determination was made for the analysis of destructive (using super pure nitric acid and adsorbing the metal-APDC and metal-Dz complexes on activated charcoal) and nondestructive (dry seeds) samples. The method is simple, precise and sensitive for the determination of microamounts of the elements (ppM to ppB).

  11. Determination of trace elements in Pre-Hispanic ceramics from Chile's Central Zone using instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Andonie, O; Munoz, L; Kohnnenkamp, I; Falabella, F

    2000-01-01

    The determination of the element composition in archaeological ceramics is an often unexplored potential, that could provide a unique set of data to verify regional economic and socio-political hypotheses. By chemically defining the elements in these materials, their manufacturing and production centers may be identified, as well as the territorial and social organization of the peoples. Appropriate analytical methodologies for this type of research are limited since there are strict requirements with reference to precision, sensitivity and detection limits, all characteristics that the activation analysis technique provides. The Chilean Nuclear Energy Commission, the University of Chile, the Smithsonian Institution and the International Atomic Energy Agency developed together a cooperative interregional project to promote interdisciplinary research, to resolve archaeological problems and to develop a new application for a nuclear analytical technique. Until this work was undertaken, no systematic studies of trace elements in archaeological ceramics had been done in Chile using the technique of Instrumental Neutron Activation Analysis (INAA). This analytical technique was used in this research to chemically characterize archaeological pieces with the sensitivity, precision and accuracy needed to be able to work with mathematical models that can or cannot establish relationships between the different samples. Protocols were defined first for preparing the pottery samples in order to generate representative samples that could be analyzed by INAA. The homogeneity in preparing the samples used was defined using a group of elements that could be determined by INAA with a precision under 2%. A group of 18 elements was selected and an analytical test procedure was planned that included the type of packaging for the irradiation, the irradiation times, decline and count, the standards to be used and the type of monitor for correcting the neutron flow. The methodology used

  12. Studies on the determination of trace amounts of nitrogen along with alkali and alkaline earth elements in uranium based samples by ion-chromatography (IC)

    International Nuclear Information System (INIS)

    Verma, Poonam; Rastogi, R.K.; Ramakumar, K.L.

    2006-12-01

    Present report describes an ion chromatography (IC) method with suppressed conductivity detection for the determination of traces of nitrogen along with alkali and alkaline earth elements in uranium based nuclear fuels. Method was developed to determine nitrogen as NH 4 + along with alkali and alkaline earth cations by IC using a cation exchange column. (author)

  13. Determination of 25 trace impurity elements in U3O8 by horizontal ICP-AES after separation with TBP levextrel resin chromatography

    International Nuclear Information System (INIS)

    Guan Jingsu; Shi Youqing; Gao Binghua; Liu Yingmei

    1988-01-01

    A method for the determination of Al, As, Ba, Be, Bi, Ca, Cd, Cu, Co, Cr, Fe, Mg, Mn, Mo, Ni, P, Pb, Ru, Sb, Sn, Sr, Ti, V, W and Zn 25 trace elements in U 3 O 8 is reported. The sample is dissolved in HNO 3 or HNO 3 -HCLO 4 -HF and the uranium is separated by TBP Levextrel resin chromatogyaphy. The impurity elements containing in the aquaous phase are determined by horizontal ICp-AES method. With a sample of 300 mg, the detection limit for all the 25 elements is in the range of 0.01∼5ppm, the recovery is in the range of 82∼ 121%, the determination precision (RSD) is less than ±13%. 18 trace elements in reference material of U 3 O 8 prepared in China are determined, the values obtained well with the values of overall median of accepted laboratory means

  14. Trace element analysis in soy sauce

    International Nuclear Information System (INIS)

    Haruyama, Yoichi; Saito, Manabu; Tomiya, Michio

    1993-01-01

    Trace elements in soy sauce have been measured by means of in-air PIXE. Six kinds of trace elements were detected, such as Mn, Fe, Ni, Zn, Cu and Br. Concentrations of Mn, Fe, Zn and Br which were observed in all samples, have been determined. Each analyzed sample contained considerable amount of Br about 160 ppm. Comparison of Br content of the imported raw materials with those of the domestic ones suggested that the large amount of Br was the residual fumigation chemicals in the imported raw materials. (author)

  15. Comparative evaluation of trace elements in blood

    International Nuclear Information System (INIS)

    Goeij, J.J.M. de; Tjioe, P.S.; Pries, C.; Zwiers, J.H.L.

    1976-01-01

    The Interuniversitair Reactor Instituut and the Centraal Laboratorium TNO have carried out a common investigation on neutron-activation-analytical procedures for the determination of trace elements in blood. A comparative evaluation of five methods, destructive as well as non-destructive, is given. The sensitivity and reproducibility of the procedures are discussed. By combining some of the methods it is possible, starting with 1 ml blood, to give quantitative information on 14 important trace elements: antimony, arsenic, bromine, cadmium, cobalt, gold, copper, mercury, molybdenum, nickel, rubidium, selenium, iron and zinc. The methods have also been applied to sodium, chromium and potassium

  16. A simple chemical method for the separation of phosphorus interfering the trace element determinations by neutron activation analysis in high doped silicon wafers

    International Nuclear Information System (INIS)

    Wagler, H.; Flachowsky, J.

    1986-01-01

    Neutron activation analysis is one of the most available method for the determination of trace elements, but in the case of P-doped silicon wafers the 32 P-activity interferes the gamma spectrometry. It is not possible to determine the trace elements without chemical manipulations. On the other hand, time consuming chemical separations should be avoided. Therefore, a simple and rapid P-separation method has to be developed, in which the following twelve trace elements should be taken into consideration: Ag, As, Au, Co, Cr, Cu, Fe, Mo, Na, Sb, W, and Zn. After acid oxidative dissolution of the activated sample, P is present as phosphate ion. The phosphate ion is removed by precipitation as BiPO 4 . (author)

  17. Trace elements distribution in environmental compartments

    International Nuclear Information System (INIS)

    Queiroz, Juliana C. de; Peres, Sueli da Silva; Godoy, Maria Luiza D.P.

    2017-01-01

    Trace elements term defines the presence of low concentrations metals at environment. Some of them are considered biologically essential, as Co, Cu and Mn. Others can cause detriment to environment and human health, as Pb, Cd, Hg, As, Ti and U. A large number of them have radioactive isotopes, implying the evaluation of risks for human health should be done considering the precepts of environmental radiological protection. The ecosystem pollution with trace elements generates changes at the geochemistry cycle of these elements and in environmental quality. Soils have single characteristics when compared with another components of biosphere (air, water and biota), cause they introduce themselves not only as a drain towards contaminants, but also as natural buffer that control the transport of chemical elements and other substances for atmosphere, hydrosphere and biota. The main purpose of environmental monitoring program is to evaluate the levels of contaminants in the various compartments of the environment: natural or anthropogenic, and to assess the contribution of a potential contaminant source on the environment. Elemental Composition for the collected samples was determined by inductively coupled plasma mass spectroscopy. The main objective of this work was to evaluate the map baseline of concentration of interest trace elements in environmental samples of water, sediment and soil from Environmental Monitoring Program of Instituto de Radioprotecao e Dosimetria (IRD). The samples were analyzed using an inductively coupled plasma mass spectrometer (ICP-MS) at IRD. >From the knowledge of trace elements concentrations, could be evaluated the environmental quality parameters at the studied ecosystems. The data allowed evaluating some relevant aspects of the study of trace elements in soil and aquatic systems, with emphasis at the distribution, concentration and identification of main anthropic sources of contamination at environment. (author)

  18. Trace elements distribution in environmental compartments

    Energy Technology Data Exchange (ETDEWEB)

    Queiroz, Juliana C. de; Peres, Sueli da Silva; Godoy, Maria Luiza D.P., E-mail: suelip@ird.gov.br [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

    2017-11-01

    Trace elements term defines the presence of low concentrations metals at environment. Some of them are considered biologically essential, as Co, Cu and Mn. Others can cause detriment to environment and human health, as Pb, Cd, Hg, As, Ti and U. A large number of them have radioactive isotopes, implying the evaluation of risks for human health should be done considering the precepts of environmental radiological protection. The ecosystem pollution with trace elements generates changes at the geochemistry cycle of these elements and in environmental quality. Soils have single characteristics when compared with another components of biosphere (air, water and biota), cause they introduce themselves not only as a drain towards contaminants, but also as natural buffer that control the transport of chemical elements and other substances for atmosphere, hydrosphere and biota. The main purpose of environmental monitoring program is to evaluate the levels of contaminants in the various compartments of the environment: natural or anthropogenic, and to assess the contribution of a potential contaminant source on the environment. Elemental Composition for the collected samples was determined by inductively coupled plasma mass spectroscopy. The main objective of this work was to evaluate the map baseline of concentration of interest trace elements in environmental samples of water, sediment and soil from Environmental Monitoring Program of Instituto de Radioprotecao e Dosimetria (IRD). The samples were analyzed using an inductively coupled plasma mass spectrometer (ICP-MS) at IRD. >From the knowledge of trace elements concentrations, could be evaluated the environmental quality parameters at the studied ecosystems. The data allowed evaluating some relevant aspects of the study of trace elements in soil and aquatic systems, with emphasis at the distribution, concentration and identification of main anthropic sources of contamination at environment. (author)

  19. Geochemical cycling and depositional patterns across the northeast region of the Greenland Ice Sheet as determined from trace element chemistry

    Science.gov (United States)

    Wong, G. J.; Osterberg, E. C.; Courville, Z.; Hawley, R. L.; Lutz, E.; Overly, T. B.

    2012-12-01

    The Greenland Ice Sheet is both a repository of climate history and a major driver in Arctic and global climate. Between 1952 and 1955, Carl Benson led a series of traverses of the Greenland Ice Sheet (GIS), and characterized the GIS via mapping of the spatial distribution of annual net accumulation and classifying the diagenetic glacier facies (Benson, 1962). While polar ice sheets represent a unique archive of past atmospheric and climatic conditions, little information exists on large-scale geographical trends in trace element snow chemistry across GIS because of the remote, challenging location. In the spring of 2011, we undertook a 1120 km traverse of the GIS from Thule Air Base to Summit Station. Samples from 11 snow pits and 3 firn cores, dated by stable water isotopes, were analyzed and evaluated in seasonal resolution for their trace element content (23Na, 24Mg, 27Al, 32S, 39K, 44Ca, 47Ti, 51V, 52Cr, 55Mn, 56Fe, 59Co, 63Cu, 66Zn, 75As, 88Sr, 111Cd, 133Cs, 138Ba, 139La, 140Ce, 141Pr, 208Pb, 209Bi, 238U). Here, we present an initial analysis of the spatial gradients of these trace elements and an interpretation of how their depositional patterns characterize the GIS. The seasonal trends coupled with spatial variability of certain trace elements establish the behavior of specific aerosols (e.g. dust, sea salt, pollution), which will be useful in quantifying geochemical cycling across the GIS and comparing characterizations with results from Benson's traverses. Benson, CS. 1962. Stratigraphic studies in the snow and firn of the Greenland Ice Sheet. SIPRE Research Report, 70, 89 pp.

  20. Determination of trace element mineral/liquid partition coefficients in melilite and diopside by ion and electron microprobe techniques

    Science.gov (United States)

    Kuehner, S. M.; Laughlin, J. R.; Grossman, L.; Johnson, M. L.; Burnett, D. S.

    1989-01-01

    The applicability of ion microprobe (IMP) for quantitative analysis of minor elements (Sr, Y, Zr, La, Sm, and Yb) in the major phases present in natural Ca-, Al-rich inclusions (CAIs) was investigated by comparing IMP results with those of an electron microprobe (EMP). Results on three trace-element-doped glasses indicated that it is not possible to obtain precise quantitative analysis by using IMP if there are large differences in SiO2 content between the standards used to derive the ion yields and the unknowns.

  1. Trace Elements in Cardiovascular Diseases

    Energy Technology Data Exchange (ETDEWEB)

    Masironi, R. [Cardiovascular Diseases Unit, World Health Organization, Geneva (Switzerland)

    1970-07-01

    Cardiovascular diseases are the leading cause of death in industrialized countries. Their incidence increases, apparently, as a, function of technological progress so that in the future they may become a major public health problem in developing countries too. Early diagnosis and prevention are the tools best suited to curb such an alarming trend, but our knowledge of these topics is unsatisfactory, Valuable information would be obtained through a systematic investigation of trace elements in relation to cardiovascular function and to various types of cardiovascular diseases. Such studies would provide clues to the following questions: 1. Why does the incidence and type of cardiovascular disease differ from one country to another? May this be related to differences in tissue mineral concentrations among various population groups? 2. Which trace elements if any are beneficial to cardiovascular health, and which are harmful ones that may act as aetiological agents for some cardiovascular diseases? 3. Is it possible to utilize measurements of mineral element concentration for diagnostic purposes in cardiovascular disease? (author)

  2. Use of Instrumental Neutron Activation Analysis for Determination of Some Trace Elements of Biological Importance in Different Jute(Corchorus Capsularis) Seed Samples

    International Nuclear Information System (INIS)

    Metwally, E.; Abd-El-Khalik, H.; El-Sweify, F.H.; El-Sweify, A.H.H.

    2004-01-01

    Instrumental neutron activation analysis technique was used to determine some trace elements in seeds of jute (corchorus capsularis). The seed samples were obtained from Agricultural Research Center (ARC), Giza, (EG). The analyzed seed samples were produced from cultivation of three different strains, namely: St. DC 1105, st. JRC 7447 and St. PADMA. These strains were imported from Bangladesh. The jute plant was cultivated in sandy soil in Ismailaya research station farm at may on two seasons 1999 and 2000. The plant was irrigated with water from Ismailaya canal. The study was carried out to compare the influence of applying different kinds of fertilizers of different rates, i.e. mineral fertilizer and biofertilizer, on the uptake of some biologically important trace elements and to determine their concentration in the analyzed jute seed samples. These elements were; Co,Cr,Fe,Zn and others eight elements were analyzed quantitatively

  3. Determination of trace elements in the human hair reference material, HH-I, by neutron activation analysis and atomic absorption spectrophotometry

    International Nuclear Information System (INIS)

    Coetzee, P.; Pieterse, H.

    1986-01-01

    Analytical procedures are presented and problem areas identified with regard to the determination of trace elements in IAEA powdered human hair reference material, HH-I, of limited sample size (100-200 mg), by NAA and graphite furnace AAS. Results obtained for the twelve elements As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Sb, Se, and Zn studied in human hair and other biological reference material like orchard leaves, seaplant material, and copepod compare satisfactorily with the certified values

  4. Development of a certified reference material (NMIJ CRM 7512-a) for the determination of trace elements in milk powder.

    Science.gov (United States)

    Zhu, Yanbei; Narukawa, Tomohiro; Miyashita, Shin-ichi; Kuroiwa, Takayoshi; Inagaki, Kazumi; Chiba, Koichi; Hioki, Akiharu

    2013-01-01

    A certified reference material (CRM), NMIJ CRM 7512-a, was developed for the determination of trace elements in milk powder. At least three independent analytical methods were applied to characterize the certified value of each element; all of these analytical methods were based on microwave acid digestions and carried out using different analytical instruments. The certified value was given on a dry-mass basis, where the dry-mass correction factor was obtained by drying the sample at 65°C for 15 to 25 h. The certified values in the units of mass fractions for 13 elements were as follows: Ca, 8.65 (0.38) g kg(-1); Fe, 0.104 (0.007) g kg(-1); K, 8.41 (0.33) g kg(-1); Mg, 0.819 (0.024) g kg(-1); Na, 1.87 (0.09) g kg(-1); P, 5.62 (0.23) g kg(-1); Ba, 0.449 (0.013) mg kg(-1); Cu, 4.66 (0.23) mg kg(-1); Mn, 0.931 (0.032) mg kg(-1); Mo, 0.223 (0.012) mg kg(-1); Rb, 8.93 (0.31) mg kg(-1); Sr, 5.88 (0.20) mg kg(-1); and Zn, 41.3 (1.4) mg kg(-1), where the numbers in the parentheses are the expanded uncertainties with a coverage factor of 2. The expanded uncertainties were estimated considering the contribution of the analytical methods, the method-to-method variance, the sample homogeneity, the dry-mass correction factor, and the concentrations of the standard solutions for calibration. The concentrations of As (2.1 μg kg(-1)), Cd (0.2 μg kg(-1)), Cr (1.3 μg kg(-1)), Pb (0.3 μg kg(-1)), and Y (64 μg kg(-1)) were given as information values for the present CRM.

  5. Direct determination of trace elements in boron nitride powders by slurry sampling total reflection X-ray fluorescence spectrometry

    International Nuclear Information System (INIS)

    Amberger, Martin A.; Hoeltig, Michael; Broekaert, Jose A.C.

    2010-01-01

    The use of slurry sampling total reflection X-ray fluorescence spectrometry (SlS-TXRF) for the direct determination of Ca, Cr, Cu, Fe, Mn and Ti in four boron nitride powders has been described. Measurements of the zeta potential showed that slurries with good stabilities can be obtained by the addition of polyethylenimine (PEI) at a concentration of 0.1 wt.% and by adjusting the pH at 4. For the optimization of the concentration of boron nitride in the slurries the net line intensities and the signal to background ratios were determined for the trace elements Ca and Ti as well as for the internal standard element Ga in the case of concentrations of boron nitride ranging from 1 to 30 mg mL -1 . As a compromise with respect to high net line intensities and high signal to background ratios, concentrations of 5 mg mL -1 of boron nitride were found suitable and were used for all further measurements. The limits of detection of SlS-TXRF for the boron nitride powders were found to range from 0.062 to 1.6 μg g -1 for Cu and Ca, respectively. Herewith, they are higher than those obtained in solid sampling and slurry sampling graphite furnace atomic absorption spectrometry (SoS-GFAAS, SlS-GFAAS) as well as those of solid sampling electrothermal evaporation inductively coupled plasma optical emission spectrometry (SoS-ETV-ICP-OES). For Ca and Fe as well as for Cu and Fe, however, they were found to be lower than for GFAAS and for ICP-OES subsequent to wet chemical digestion, respectively. The universal applicability of SlS-TXRF to the analysis of samples with a wide variety of matrices could be demonstrated by the analysis of certified reference materials such as SiC, Al 2 O 3 , powdered bovine liver and borate ore with a single calibration. The correlation coefficients of the plots for the values found for Ca, Fe and Ti by SlS-TXRF in the boron nitride powders as well as in the before mentioned samples versus the reference values for the respective samples over a

  6. Direct determination of trace elements in boron nitride powders by slurry sampling total reflection X-ray fluorescence spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Amberger, Martin A.; Hoeltig, Michael [University of Hamburg, Institute for Inorganic and Applied Chemistry, Martin-Luther-King-Platz 6, D-20146 Hamburg (Germany); Broekaert, Jose A.C., E-mail: jose.broekaert@chemie.uni-hamburg.d [University of Hamburg, Institute for Inorganic and Applied Chemistry, Martin-Luther-King-Platz 6, D-20146 Hamburg (Germany)

    2010-02-15

    The use of slurry sampling total reflection X-ray fluorescence spectrometry (SlS-TXRF) for the direct determination of Ca, Cr, Cu, Fe, Mn and Ti in four boron nitride powders has been described. Measurements of the zeta potential showed that slurries with good stabilities can be obtained by the addition of polyethylenimine (PEI) at a concentration of 0.1 wt.% and by adjusting the pH at 4. For the optimization of the concentration of boron nitride in the slurries the net line intensities and the signal to background ratios were determined for the trace elements Ca and Ti as well as for the internal standard element Ga in the case of concentrations of boron nitride ranging from 1 to 30 mg mL{sup -1}. As a compromise with respect to high net line intensities and high signal to background ratios, concentrations of 5 mg mL{sup -1} of boron nitride were found suitable and were used for all further measurements. The limits of detection of SlS-TXRF for the boron nitride powders were found to range from 0.062 to 1.6 mug g{sup -1} for Cu and Ca, respectively. Herewith, they are higher than those obtained in solid sampling and slurry sampling graphite furnace atomic absorption spectrometry (SoS-GFAAS, SlS-GFAAS) as well as those of solid sampling electrothermal evaporation inductively coupled plasma optical emission spectrometry (SoS-ETV-ICP-OES). For Ca and Fe as well as for Cu and Fe, however, they were found to be lower than for GFAAS and for ICP-OES subsequent to wet chemical digestion, respectively. The universal applicability of SlS-TXRF to the analysis of samples with a wide variety of matrices could be demonstrated by the analysis of certified reference materials such as SiC, Al{sub 2}O{sub 3}, powdered bovine liver and borate ore with a single calibration. The correlation coefficients of the plots for the values found for Ca, Fe and Ti by SlS-TXRF in the boron nitride powders as well as in the before mentioned samples versus the reference values for the respective

  7. Trace elements in wild and orchard honeys

    Energy Technology Data Exchange (ETDEWEB)

    Almeida-Silva, M.; Canha, N.; Galinha, C.; Dung, H.M. [Instituto Tecnologico e Nuclear, URSN, E.N. 10, 2686-953 Sacavem (Portugal); Freitas, M.C., E-mail: cfreitas@itn.pt [Instituto Tecnologico e Nuclear, URSN, E.N. 10, 2686-953 Sacavem (Portugal); Sitoe, T. [Instituto Tecnologico e Nuclear, URSN, E.N. 10, 2686-953 Sacavem (Portugal)

    2011-11-15

    The present study aims the identification and quantification of trace elements in two types of honey samples: Orchard honey and Wild honey from mainland Portugal. Chemical elements content was assessed by Instrumental Neutron Activation Analysis (INAA). Concentrations were determinated for Ag, As, Br, Ca, Cl, Cs, Cu, Fe, K, La, Mg, Mn, Na, Rb, Sb, Sc, U, V and Zn. The nutritional values of both honey types were evaluated since this product contains some elements that are essential dietary nutrients for humans. Physical properties of the honey samples, such as electrical conductivy and pH, were assessed as well.

  8. A new method based on low background instrumental neutron activation analysis for major, trace and ultra-trace element determination in atmospheric mineral dust from polar ice cores

    Energy Technology Data Exchange (ETDEWEB)

    Baccolo, Giovanni, E-mail: giovanni.baccolo@mib.infn.it [Graduate School in Polar Sciences, University of Siena, Via Laterina 8, 53100, Siena (Italy); Department of Environmental Sciences, University of Milano-Bicocca, P.zza della Scienza 1, 20126, Milano (Italy); INFN, Section of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Clemenza, Massimiliano [INFN, Section of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Department of Physics, University of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Delmonte, Barbara [Department of Environmental Sciences, University of Milano-Bicocca, P.zza della Scienza 1, 20126, Milano (Italy); Maffezzoli, Niccolò [Centre for Ice and Climate, Niels Bohr Institute, Juliane Maries Vej, 30, 2100, Copenhagen (Denmark); Nastasi, Massimiliano; Previtali, Ezio [INFN, Section of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Department of Physics, University of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy); Prata, Michele; Salvini, Andrea [LENA, University of Pavia, Pavia (Italy); Maggi, Valter [Department of Environmental Sciences, University of Milano-Bicocca, P.zza della Scienza 1, 20126, Milano (Italy); INFN, Section of Milano-Bicocca, P.zza della Scienza 3, 20126, Milano (Italy)

    2016-05-30

    Dust found in polar ice core samples present extremely low concentrations, in addition the availability of such samples is usually strictly limited. For these reasons the chemical and physical analysis of polar ice cores is an analytical challenge. In this work a new method based on low background instrumental neutron activation analysis (LB-INAA) for the multi-elemental characterization of the insoluble fraction of dust from polar ice cores is presented. Thanks to an accurate selection of the most proper materials and procedures it was possible to reach unprecedented analytical performances, suitable for ice core analyses. The method was applied to Antarctic ice core samples. Five samples of atmospheric dust (μg size) from ice sections of the Antarctic Talos Dome ice core were prepared and analyzed. A set of 37 elements was quantified, spanning from all the major elements (Na, Mg, Al, Si, K, Ca, Ti, Mn and Fe) to trace ones, including 10 (La, Ce, Nd, Sm, Eu, Tb, Ho, Tm, Yb and Lu) of the 14 natural occurring lanthanides. The detection limits are in the range of 10{sup −13}–10{sup −6} g, improving previous results of 1–3 orders of magnitude depending on the element; uncertainties lies between 4% and 60%. - Highlights: • A new method based on neutron activation for the multi-elemental characterization of atmospheric dust entrapped in polar ice cores is proposed. • 37 elements were quantified in μg size dust samples with detection limits ranging from 10{sup −13} to 10{sup −6} g. • A low background approach and a clean analytical protocol improved INAA performances to unprecedented levels for multi-elemental analyses.

  9. Determination of Mineral, Trace Element, and Pesticide Levels in Honey Samples Originating from Different Regions of Malaysia Compared to Manuka Honey

    Science.gov (United States)

    Moniruzzaman, Mohammed; Chowdhury, Muhammed Alamgir Zaman; Rahman, Mohammad Abdur; Sulaiman, Siti Amrah; Gan, Siew Hua

    2014-01-01

    The present study was undertaken to determine the content of six minerals, five trace elements, and ten pesticide residues in honeys originating from different regions of Malaysia. Calcium (Ca), magnesium (Mg), iron (Fe), and zinc (Zn) were analyzed by flame atomic absorption spectrometry (FAAS), while sodium (Na) and potassium (K) were analyzed by flame emission spectrometry (FAES). Trace elements such as arsenic (As), lead (Pb), cadmium (Cd), copper (Cu), and cobalt (Co) were analyzed by graphite furnace atomic absorption spectrometry (GFAAS) following the microwave digestion of honey. High mineral contents were observed in the investigated honeys with K, Na, Ca, and Fe being the most abundant elements (mean concentrations of 1349.34, 236.80, 183.67, and 162.31 mg/kg, resp.). The concentrations of the trace elements were within the recommended limits, indicating that the honeys were of good quality. Principal component analysis reveals good discrimination between the different honey samples. The pesticide analysis for the presence of organophosphorus and carbamates was performed by high performance liquid chromatography (HPLC). No pesticide residues were detected in any of the investigated honey samples, indicating that the honeys were pure. Our study reveals that Malaysian honeys are rich sources of minerals with trace elements present within permissible limits and that they are free from pesticide contamination. PMID:24982869

  10. Determination of Mineral, Trace Element, and Pesticide Levels in Honey Samples Originating from Different Regions of Malaysia Compared to Manuka Honey

    Directory of Open Access Journals (Sweden)

    Mohammed Moniruzzaman

    2014-01-01

    Full Text Available The present study was undertaken to determine the content of six minerals, five trace elements, and ten pesticide residues in honeys originating from different regions of Malaysia. Calcium (Ca, magnesium (Mg, iron (Fe, and zinc (Zn were analyzed by flame atomic absorption spectrometry (FAAS, while sodium (Na and potassium (K were analyzed by flame emission spectrometry (FAES. Trace elements such as arsenic (As, lead (Pb, cadmium (Cd, copper (Cu, and cobalt (Co were analyzed by graphite furnace atomic absorption spectrometry (GFAAS following the microwave digestion of honey. High mineral contents were observed in the investigated honeys with K, Na, Ca, and Fe being the most abundant elements (mean concentrations of 1349.34, 236.80, 183.67, and 162.31 mg/kg, resp.. The concentrations of the trace elements were within the recommended limits, indicating that the honeys were of good quality. Principal component analysis reveals good discrimination between the different honey samples. The pesticide analysis for the presence of organophosphorus and carbamates was performed by high performance liquid chromatography (HPLC. No pesticide residues were detected in any of the investigated honey samples, indicating that the honeys were pure. Our study reveals that Malaysian honeys are rich sources of minerals with trace elements present within permissible limits and that they are free from pesticide contamination.

  11. Determination of mineral, trace element, and pesticide levels in honey samples originating from different regions of Malaysia compared to manuka honey.

    Science.gov (United States)

    Moniruzzaman, Mohammed; Chowdhury, Muhammed Alamgir Zaman; Rahman, Mohammad Abdur; Sulaiman, Siti Amrah; Gan, Siew Hua

    2014-01-01

    The present study was undertaken to determine the content of six minerals, five trace elements, and ten pesticide residues in honeys originating from different regions of Malaysia. Calcium (Ca), magnesium (Mg), iron (Fe), and zinc (Zn) were analyzed by flame atomic absorption spectrometry (FAAS), while sodium (Na) and potassium (K) were analyzed by flame emission spectrometry (FAES). Trace elements such as arsenic (As), lead (Pb), cadmium (Cd), copper (Cu), and cobalt (Co) were analyzed by graphite furnace atomic absorption spectrometry (GFAAS) following the microwave digestion of honey. High mineral contents were observed in the investigated honeys with K, Na, Ca, and Fe being the most abundant elements (mean concentrations of 1349.34, 236.80, 183.67, and 162.31 mg/kg, resp.). The concentrations of the trace elements were within the recommended limits, indicating that the honeys were of good quality. Principal component analysis reveals good discrimination between the different honey samples. The pesticide analysis for the presence of organophosphorus and carbamates was performed by high performance liquid chromatography (HPLC). No pesticide residues were detected in any of the investigated honey samples, indicating that the honeys were pure. Our study reveals that Malaysian honeys are rich sources of minerals with trace elements present within permissible limits and that they are free from pesticide contamination.

  12. Determination of trace elements in dried sea-plant homogenate (SP-M-1) and in dried copepod homogenate (MA-A-1) by means of neutron activation analysis

    International Nuclear Information System (INIS)

    Tjioe, P.S.; Goeij, J.J.M. de; Bruin, M. de.

    1977-07-01

    Two marine environmental reference materials were investigated in an intercalibration study of trace elements. According to the specifications from the International Laboratory of Marine Radioactivity at Monaco two samples, a sea-plant homogenate and a copepod homogenate, were analysed by neutron activation analysis. The results of the trace-element analyses were based on dry weight. The moisture content was measured on separate aliquots. For the intercalibration study the following elements were listed as elements of primary interest: mercury, cadmium, lead, manganese, zinc, copper, chromium, silver, iron and nickel. For the 14 elements normally analysed with the routine destructive method, the element gold could not be measured in the two marine samples. This was due to the high residual bromine-82 activity in fraction 13, which contains gold that distills over. With the nondestructive method, nine elements could be assessed, of which only three coincide with the 14 elements of the destructive method. A survey of all measured (trace) elements is presented. The 20 (trace) elements measured in the sea-plant homogenate and in the copepod homogenate comprise 8 out of the 10 trace elements of primary interest, all 5 trace elements of secondary interest (arsenic, cobalt, antimony, selenium and vanadium), and 5 additional (trace) elements. The trace-element determination in both marine biological materials via the destructive procedure was carried out in twelve-fold. In the nondestructive procedure quadruple measurements were performed. For all trace-element levels analysed an average value was calculated

  13. The validation of a method for determining the migration of trace elements from food packaging materials into food

    International Nuclear Information System (INIS)

    Thompson, D.; Parry, S.J.; Benzing, R.

    1997-01-01

    A new radiotracer method has been developed to measure the migration of trace elements from food contact packaging into four standard food simulants; acetic acid, ethanol, olive oil, deionised water. A sample of material is irradiated in a thermal neutron flux of 10 16 n x m -2 x s -1 to activate the trace elements and produce a range of radionuclides. The samples is then placed in the food simulant and the migration of the radionuclides is monitored by performing γ-ray spectrometry on a sample of the simulant. Any radionuclides measured must be due entirely to the migration of the elements present in the plastic, since the simulant itself is not radioactive. Preliminary studies have shown that detection limits of around 0.2 μg x dm -2 (0.002 mg/kg) can be achieved for antimony in a sample of polyethylene terephthalate. This method can now been extended to measure migration into real foods. This will highlight any differences between the standard simulants currently used and real foods. Since the method only involves irradiation of the packaging material any food matrix can be studied. (author)

  14. Trace elements in Australian opals using neutron activation analysis

    International Nuclear Information System (INIS)

    McOrist, G.D.; Fardy, J.J.

    1994-01-01

    Neutron activation analysis was used to determine the concentration of trace elements in 42 samples of black, grey and white opals taken from a number of recognised Australian field. The results were evaluated to determine if a relationship exited between trace element content and opal colour. (author) 12 refs.; 12 figs.; 3 tabs

  15. Method 200.12 - Determination of Trace Elements in Marine Waters by StabilizedTemperature Graphite Furnace Atomic Absorption

    Science.gov (United States)

    This method provides procedures for the determination of total recoverable elements by graphite furnace atomic absorption (GFAA) in marine waters, including estuarine, ocean and brines with salinities of up to 35 ppt.

  16. Zinc: a multipurpose trace element

    Energy Technology Data Exchange (ETDEWEB)

    Stefanidou, M.; Maravelias, C.; Dona, A.; Spiliopoulou, C. [University of Athens, Department of Forensic Medicine and Toxicology, Athens (Greece)

    2006-01-01

    Zinc (Zn) is one of the most important trace elements in the body and it is essential as a catalytic, structural and regulatory ion. It is involved in homeostasis, in immune responses, in oxidative stress, in apoptosis and in ageing. Zinc-binding proteins (metallothioneins, MTs), are protective in situations of stress and in situations of exposure to toxic metals, infections and low Zn nutrition. Metallothioneins play a key role in Zn-related cell homeostasis due to their high affinity for Zn, which is in turn relevant against oxidative stress and immune responses, including natural killer (NK) cell activity and ageing, since NK activity and Zn ion bioavailability decrease in ageing. Physiological supplementation of Zn in ageing and in age-related degenerative diseases corrects immune defects, reduces infection relapse and prevents ageing. Zinc is not stored in the body and excess intakes result in reduced absorption and increased excretion. Nevertheless, there are cases of acute and chronic Zn poisoning. (orig.)

  17. Evaluation of the impact of general phosphate fertilizers factories company on the surrounding environment by determining natural radionuclides and some trace elements in air particulates

    International Nuclear Information System (INIS)

    Al-Masri, M. S.; Al-Kharfan, K.; Al-Hamwi, A.; Al-Shamali, K.

    2004-01-01

    Natural radionuclides and some trace element levels in air particulates of the areas surrounding the phosphate fertilizers factory in Homs have been determined Mean total air particulates concentration ranged from 31 μg/m3 in Kerba Al-Teen in Autumn period. While trace element concentrations in air particulates were relatively high in air particulates collected from AECS center and other sites situated north east of the factory; about 1.7 ng/m3 in AECS site and 1.7 ng/m3 in Abel for uranium and cadmium, respectively. In addition, radioactivity analysis of air particulates has shown low levels of polonium 210 and lead 210; a value of 2 mBq/m3 in Kerba Al-Teen has not been exceeded. However, air particulate, natural radionuclides and the studied trace elements concentrations in the surrounding areas were within the natural levels. Therefore, air emissions from the factory containing radioactive materials and trace elements are relatively low. This is due to strict control procedures on transport and loading processes of phosphate in addition to the high efficiency of filters used for air emissions from the phosphate fertilizers factory during the study period (2002). (author)

  18. Report on the intercomparison of determination of selected radionuclides and trace elements in water (W-1, W-2 and W-3, 1975-76)

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1976-12-01

    Water is one of the most common materials which are analyzed for the purpose of monitoring of environmental pollution. While being an apparently 'easy' matrix it can in fact pose serious problems even for an experienced analyst. Trace elements and radionuclides may 'disappear' from aqueous solutions due to adsorption on container walls and some of them due to volatilization, bacterial action, etc. Preconcentration techniques such as evaporation and freeze-drying may also lead to considerable losses of some elements. On the other hand, when the vessels employed for storing the water samples have not been adequately cleaned, some trace elements may be 'added' to the solution. The above mentioned difficulties can probably, at least in part, account for the fact that only a small part of the participating laboratories sent in their results before the original deadline. Even after setting the new deadline (30 January 1976) the results were flowing in very sluggishly over a period of a few months what obviously delayed the preparation of this report. Altogether 46 laboratories participated in the W-1 and W-2 runs and 35 in the W-3 run but only a few determined all or most of radionuclides or trace elements, respectively. The present intercomparisons were intended to provide the opportunity of checking up the analytical performance for the laboratories dealing with low level activity measurements in water as well as for those engaged in trace multielement analysis.

  19. Evaluation of the impact of general phosphate fertilizers factories company on the surrounding environment by determining natural radionuclides and some trace elements in air particulates

    International Nuclear Information System (INIS)

    Al-Masri, M. S.; Al-Kharfan, K.; Al-Hamwi, A.; Al-Shmali, K.; Abdul Haleem, M.

    2003-12-01

    Natural radionuclides and some trace element levels in air particulates of the areas surrounding the phosphate fertilizers factory in Homs have been determined mean total air particulates concentration ranged from 31μg/m 3 in Kerba Al-Teen in autumn period. While trace element concentrations in air particulates were relatively high in air particulates collected from AECS center and other sites situated north east of the factory: about 1.7 ng/m 3 in AECS site and 1.7 ng/m 3 in Abel for uranium and cadmium, respectively. In addition, radioactivity analysis of air particulates have shown low levels of polonium 210 and lead 210, a value of 2 mBg/m 3 in Kerba Al-Teen has not been exceeded. However, air particulate, natural radionuclides and the studied trace elements concentrations in the surrounding areas were within the natural levels. Therefore, air emissions from the factory containing radioactive materials and trace elements are relatively low. This is due to strict control procedures on transport and loading processes of phosphate in addition to the high efficiency of filters used for air emissions from the phosphate fertilizers factory during the study period (2002).(author)

  20. Evaluation of NAA laboratory results in inter-comparison on determination of trace elements in food and environmental samples

    International Nuclear Information System (INIS)

    Diah Dwiana Lestiani; Syukria Kurniawati; Natalia Adventini

    2012-01-01

    Inter-comparison program is a good tool for improving quality and to enhance the accuracy and precision of the analytical techniques. By participating in this program, laboratories could demonstrate their capability and ensuring the quality of analysis results generated by analytical laboratories. The Neutron Activation Analysis (NAA) laboratory at National Nuclear Energy Agency of Indonesia (BATAN), Nuclear Technology Center for Materials and Radiometry-PTNBR laboratory participated in inter-comparison tests organized by NAA working group. Inter-comparison BATAN 2009 was the third inter-laboratory analysis test within that project. The participating laboratories were asked to analyze for trace elements using neutron activation analysis as the primary technique. Three materials were distributed to the participants representing foodstuff, and environmental material samples. Samples were irradiated in rabbit facility of G.A. Siwabessy reactor with neutron flux ~ 10 13 n.cm -2 .s -1 , and counted with HPGe detector of gamma spectrometry. Several trace elements in these samples were detected. The accuracy and precision evaluation based on International Atomic Energy Agency (IAEA) criteria was applied. In this paper the PTNBR NAA laboratory results is evaluated. (author)

  1. The determination of the C, N, O and trace element content of Triticum aestivum by activation analysis, X-ray excitation and mass spectrometry

    International Nuclear Information System (INIS)

    Leonhardt, J.W.; Dahn, E.; Dietze, H.J.; Freyer, K.; Geisler, M.; Hartmann, G.; Jung, K.; Schelhorn, H.

    1979-01-01

    The results of determinations of the C, N, O and trace element content of grains, sprouts and leaves of Triticum aestivum by means of various methods of activation analysis, X-ray excitation and mass spectrometry are presented. The C and O contents were determined by X-ray excitation; the O, N, P and Si contents were measured by NAA with 14-MeV neutrons, and the trace elements were determined by NAA with thermal neutrons. A mass-spectrometric survey analysis confirmed the results obtained by NAA. The use of neutron-induced nuclear reactions together with autoradiography enabled a representative picture to be formed of the spatial distribution in two dimensions of 14 N in biological specimens. (author)

  2. Trace element analysis: a diagnostic tool

    International Nuclear Information System (INIS)

    Qureshi, I.H.; Cheema, M.N.

    1976-09-01

    The human mody continuously assimilates a variety of elements from the environment, and the concentration of these elements in the blood is regulated by means of various homeostatic mechanisms. Some of the elements, though present in very small amounts, have highly specialized functions in initiating many biochemical reactions. These elements, known as essential trace elements, are closely related to human diseases since their deficiency or excess induces physiological changes. Many diseases such as hypertension, atherosclerosis, diabetes, etc., are related to an imbalance in trace element. The measurement of trace elements in body fluids and tissues can, therefore, be effectively employed for diagnostic tests

  3. Determination and statistical analysis of trace element and active constituent concentrations in the medicinal plant Eucalyptus camaldulensis Dehnh (E. rostratus Schlecht)

    International Nuclear Information System (INIS)

    Kanias, G.D.; Kilikoglou, V.; Tsitsa, E.; Loukis, A.

    1993-01-01

    In the leaves of the medicinal plant Eucalyptus camaldulensis Dehnh (E. rostratus Schlecht) collected from different sampling areas of Greece the trace elements antimony, cesium, chromium, cobalt, iron, europium, rubidium scandium, strontium, thorium and zinc were determined by Instrumental Neutron Activation Analysis. In the same samples, the essential oil was determined by steam distillation and the percent relative composition of the essential oil in 1,8-cineole, p-cymene, α-pinene by gas liquid chromatography. Also the refractive index of the essential oil was determined by a refractometer. Statistical analysis included the calculation of the correlation coefficient. Multiple correlation and cluster analysis was applied to all analytical data. The results showed that the trace elements iron, chromium, cobalt and zinc are correlated with the variation of the concentration of essential oil in the examined plant. These four elements along with rubidium and essential oil content could be used for the separation of the samples into groups related to the sampling areas. Statistically significant correlation between active constituents and some trace elements and a linear negative correlation between 1,8-cineole and refractive index were found. (author) 13 refs.; 2 figs.; 2 tabs

  4. Modification of working parameters for routine determination of trace elemental impurities in PuO2 samples by direct current arc-AES

    International Nuclear Information System (INIS)

    Pant, D.K.; Phadke, M.P.; Dapolikar, T.T.; Kapur, H.N.; Kumar, Rajendra; Dubey, K.

    2015-01-01

    In the present work we have altered the parameters of routine method to determine the trace elemental impurities in PuO 2 samples using DC arc source optically coupled with CCD based spectrometer system. The method is basically a fractional distillation technique using DC arc source, involving ignition, dilution of the sample with U 3 O 8 containing carrier mixture, arcing of the sample/standard mixture in DC arc and measurement of analyte signals by spectrometer system. In all fifteen elemental impurities including Boron and Cadmium were determined. Detection limits are comparable with ICP-AES method. (author)

  5. Applying of factor analyses for determination of trace elements distribution in water from Vardar and its tributaries, Macedonia/Greece.

    Science.gov (United States)

    Popov, Stanko Ilić; Stafilov, Trajče; Sajn, Robert; Tănăselia, Claudiu; Bačeva, Katerina

    2014-01-01

    A systematic study was carried out to investigate the distribution of fifty-six elements in the water samples from river Vardar (Republic of Macedonia and Greece) and its major tributaries. The samples were collected from 27 sampling sites. Analyses were performed by mass spectrometry with inductively coupled plasma (ICP-MS) and atomic emission spectrometry with inductively coupled plasma (ICP-AES). Cluster and R mode factor analysis (FA) was used to identify and characterise element associations and four associations of elements were determined by the method of multivariate statistics. Three factors represent the associations of elements that occur in the river water naturally while Factor 3 represents an anthropogenic association of the elements (Cd, Ga, In, Pb, Re, Tl, Cu, and Zn) introduced in the river waters from the waste waters from the mining and metallurgical activities in the country.

  6. Trace element distribution in geological crystals

    Energy Technology Data Exchange (ETDEWEB)

    Den Besten, J L; Jamieson, D N; Weiser, P S [Melbourne Univ., Parkville, VIC (Australia). School of Physics

    1997-12-31

    Channelling is a useful microprobe technique for determining the structure of crystals, but until now has not been performed on geological crystals. The composition has been investigated rather than the structure, which can further explain the origin of the crystal and provide useful information on the substitutionality of trace elements. This may then lead to applications of extraction of valuable metals and semiconductor electronics. Natural crystals of pyrite, FeS{sub 2}, which contains a substantial concentration of gold were channeled and examined to identify the channel axis orientation. Rutherford Backscattering (RBS) and Particle Induced X-Ray Emission (PIXE) spectra using MeV ions were obtained in the experiment to provide a comparison of lattice and non-lattice trace elements. 3 figs.

  7. Trace element distribution in geological crystals

    Energy Technology Data Exchange (ETDEWEB)

    Den Besten, J.L.; Jamieson, D.N.; Weiser, P.S. [Melbourne Univ., Parkville, VIC (Australia). School of Physics

    1996-12-31

    Channelling is a useful microprobe technique for determining the structure of crystals, but until now has not been performed on geological crystals. The composition has been investigated rather than the structure, which can further explain the origin of the crystal and provide useful information on the substitutionality of trace elements. This may then lead to applications of extraction of valuable metals and semiconductor electronics. Natural crystals of pyrite, FeS{sub 2}, which contains a substantial concentration of gold were channeled and examined to identify the channel axis orientation. Rutherford Backscattering (RBS) and Particle Induced X-Ray Emission (PIXE) spectra using MeV ions were obtained in the experiment to provide a comparison of lattice and non-lattice trace elements. 3 figs.

  8. Concentration of trace elements in marine organisms

    International Nuclear Information System (INIS)

    Ishii, Takaaki; Suzuki, Hamaji; Iimura, Mitsue; Koyanagi, Taku

    1976-01-01

    Information on the quality and quantity of stable trace elements in marine environments is frequently required to analyze the radioecological behavior of radionuclides released from nuclear facilities into the sea. In the present work, special attention was concentrated in determination of stable Mn, Fe, Co, Zn, Rb and Cs in marine organisms to estimate the concentration factors for these elements and corresponding radionuclides. Marine organisms (fishes, marine invertebrates and seaweeds) were collected at the seashore of Ibaragi prefecture and provided for chemical analysis after dry-ashing and wet-ashing. Atomic absorption spectrophotometry and neutron activation analysis were applied to determine the concentration of elements. The concentration of stable elements in fish muscle was independent on species of the fishes though slightly higher trends were observed in ''Usumebaru'', Sebastes nivosus for Cs, ''Ishimochi'', Nibea mitsukurii for Zn and Fe compared with other species. The concentration of Co, Zn and Fe in muscle of marine invertebrates was one order of magnitude higher than fish muscles especially in shellfishes for Co. Seaweeds showed peculiar species specificity for the concentration of stable trace elements and remarkable differences was observed between the species even among the same genus. (auth.)

  9. IBA and ICP-OES determination of trace elements in indigenous medicinal herbs and their extracts on the infertility in the human male reproductive system

    Energy Technology Data Exchange (ETDEWEB)

    Mars, J.A.; Fisher, D.; Henkel, R. [Department of Medical Bioscience, Universily of the Weslern Cape, Bellville (South Africa); Weilz, F. [Department of Biodiversily and Conservation Biology, University of the Weslern Cape, Bellville (South Africa)

    2013-07-01

    Full text: The abnormality of infertility in humans is biologically defined (Mader, 2004; Wood, 1994; Ellison, 2001) as the inability of a species to reproduce its own kind after period of 12 month of unprotected sexual intercourse/copulation. It is however difficult when one wishes to quantify the occurrence of infertility, since it is seldom expressed explicitly, but mostly in conjunction with population growth dynamics which include socio-economic factors. Various plants (herbs) have been used as treatment for infertility. These plants however have not yet been scientifically analysed. In this paper we determined the major and trace element composition of Typha capensis (rhizome and leaves) Cissampe/os capensis (Ieaves) and Hermannia cilliata, which were sourced from the Cape Flats Nature Reserve, Bellville, Western Cape Province, South Africa. The trace element concentration determination are at time cumbersome, especially when destructive analytical methods such as ICP-OES are used. For our determination, the various samples were freeze-dried. Part of the freeze-dried sample was used for ICP-OES and the other for PIXE analysis. For PIXE the dried sample was pressed into a pellet, then coated with a layer of carbon and irradiated with a 3 MeV proton beam. We report on the trace element content of the various parts of the plant and comment on the applicability of the part in male infertility. (author)

  10. IBA and ICP-OES determination of trace elements in indigenous medicinal herbs and their extracts on the infertility in the human male reproductive system

    International Nuclear Information System (INIS)

    Mars, J.A.; Fisher, D.; Henkel, R.; Weilz, F.

    2013-01-01

    Full text: The abnormality of infertility in humans is biologically defined (Mader, 2004; Wood, 1994; Ellison, 2001) as the inability of a species to reproduce its own kind after period of 12 month of unprotected sexual intercourse/copulation. It is however difficult when one wishes to quantify the occurrence of infertility, since it is seldom expressed explicitly, but mostly in conjunction with population growth dynamics which include socio-economic factors. Various plants (herbs) have been used as treatment for infertility. These plants however have not yet been scientifically analysed. In this paper we determined the major and trace element composition of Typha capensis (rhizome and leaves) Cissampe/os capensis (Ieaves) and Hermannia cilliata, which were sourced from the Cape Flats Nature Reserve, Bellville, Western Cape Province, South Africa. The trace element concentration determination are at time cumbersome, especially when destructive analytical methods such as ICP-OES are used. For our determination, the various samples were freeze-dried. Part of the freeze-dried sample was used for ICP-OES and the other for PIXE analysis. For PIXE the dried sample was pressed into a pellet, then coated with a layer of carbon and irradiated with a 3 MeV proton beam. We report on the trace element content of the various parts of the plant and comment on the applicability of the part in male infertility. (author)

  11. Determination of trace elements in scallop and fish otolith by instrumental neutron activation analysis using anti-coincidence and coincidence counting methods

    International Nuclear Information System (INIS)

    Suzuki, Shogo; Okada, Yukiko; Hirai, Shoji

    2005-01-01

    Trace element concentrations in scallop reference material and fish otolith certified reference materials prepared at the National Institute for Environmental Studies (NIES) of Japan were determined by instrumental neutron activation analysis (INAA). Nine aliquots of scallop sample (ca. 252∼507 mg) and five aliquots of fish otolith sample (ca. 502 ∼ 988 mg) and comparative standards were irradiated for a short time (10 s) at a thermal neutron flux of 1.5 x 10 12 n cm -2 s -1 (pneumatic transfer) and for a long time (6 h) at a thermal neutron flux of 3.7 x 10 12 n cm -2 s -1 (central thimble) in the Rikkyo University Research Reactor (100 kW). The irradiated samples were measured by conventional γ-ray spectrometry using a coaxial Ge detector, and by anti-coincidence and coincidence γ-ray spectrometry with a coaxial Ge detector and a well-type NaI (Tl) detector to determine as many trace elements as possible with high sensitivity. The concentrations of 34 elements of the NIES No.15 scallop reference material and 16 elements of the NIES No.22 fish otolith CRM were determined. Using the coincidence counting method to determine Se, Ba and Hf, the lower limit of the determination was improved by 2 times compared with the conventional counting method. (author)

  12. Trace element determination in presolar SiC grains by synchrotron x-ray fluorescence: Commencement of a coordinated multimethod study

    International Nuclear Information System (INIS)

    Knight, K.B.; Sutton, S.R.; Newville, M.; Davis, A.M.; Dauphas, N.; Lewis, R.S.; Amari, S.; Steele, I.M.; Savina, M.R.; Pellin, M.J.

    2008-01-01

    We determined trace element compositions of individual ∼1-3 ?m presolar SiC grains from 6 KJG grains and 26 additionally cleaned KJG grains from the Murchison CM chondrite using nondestructive synchrotron X-ray fluorescence (SXRF). Presolar SiC grains are robust remnants of stellar matter ejected from stars. They survived processing in the early solar system and retain the nucleosynthetic fingerprints of their stellar progenitors. As such, they represent unique physical probes of the interiors of stars. Presolar SiC grains are commonly analyzed by mass spectrometric techniques that determine isotopic compositions and, to some degree, elemental concentrations. These techniques, however, are destructive, and can be subject to matrix effects. Elemental composition data on presolar grains remain scarce and affected by contamination and analytical artifacts. In addition, contamination has plagued isotopic characterization of some elements such as Mo and Ba. We determined trace element compositions of individual ∼1-3 (micro)m presolar SiC grains from the Murchison CM chondrite using nondestructive synchrotron X-ray fluorescence (SXRF). Samples included the KJG fraction, and a second KJG fraction that underwent additional cleaning. As every cleaning step results in some grain loss, one goal of this study was to justify additional cleaning of grains. Six KJG grains and 26 additionally cleaned KJG grains were analyzed, with location and identities of individual grains noted for future correlated isotopic study.

  13. Development of a certified reference material (NMIJ CRM 7505-a) for the determination of trace elements in tea leaves.

    Science.gov (United States)

    Zhu, Yanbei; Narukawa, Tomohiro; Inagaki, Kazumi; Kuroiwa, Takayoshi; Chiba, Koichi

    2011-01-01

    A certified reference material (CRM) for trace elements in tea leaves has been developed in National Metrology Institute of Japan (NMIJ). The CRM was provided as a dry powder (<90 µm) after frozen pulverization of washed and dried fresh tea leaves from a tea plant farm in Shizuoka Prefecture, Japan. Characterization of the property value for each element was carried out exclusively by NMIJ with at least two independent analytical methods, including inductively coupled plasma mass spectrometry (ICP-MS), high-resolution (HR-) ICP-MS, isotope-dilution (ID-) ICP-MS, inductively coupled plasma optical emission spectrometry (ICP-OES), graphite-furnace atomic-absorption spectrometry (GF-AAS) and flame atomic-absorption spectrometry (FAAS). Property values were provided for 19 elements (Ca, K, Mg, P, Al, B, Ba, Cd, Cu, Fe, Li, Mn, Na, Ni, Pb, Rb, Sr, Zn and Co) and informative values for 18 elements (Ti, V, Cr, Y, and all of the lanthanides, except for Pm whose isotopes are exclusively radioactive). The concentration ranges of property values and informative values were from 1.59% (mass) of K to 0.0139 mg kg(-1) of Cd and from 0.6 mg kg(-1) of Ti to 0.0014 mg kg(-1) of Lu, respectively. Combined relatively standard uncertainties of the property values were estimated by considering the uncertainties of the homogeneity, analytical methods, characterization, calibration standard, and dry-mass correction factor. The range of the relative combined standard uncertainties was from 1.5% of Mg and K to 4.1% of Cd.

  14. Catalytic polarographic currents of platinum metal complexes and their application to determination of trace concentrations of the elements

    International Nuclear Information System (INIS)

    Ezerskaya, N.A.; Kiseleva, I.N.

    1984-01-01

    Several types of catalytic electrode processes with the participation of platinum metal complexes and used for the determination of the element microconcentrations have been considered in the review. It is pointed out that to measure catalytic currents of hydrogen solutions nitroso compounds, which are prepared by heating chloride complexes of Ru(3) and (4) with NaNO 2 are used. The method is applicable for ruthenium determination in commercial nitric acid solutions. Ru determination in solution of ruthenium (4) dimeric chloride complex on graphite electrode, using catalytic currents of hydrogen, surpasses in sensitivity the determination of the element, using the method of inversion voltammetry. Certain other complexes of Ru and determination methods of ruthenium in them are considered. Hydrogen catalytic currents in the complexes solutions with organic ligands are the most perspective for analysis

  15. Relationship between epiphytic lichens, trace elements and gaseous atmospheric pollutants

    NARCIS (Netherlands)

    Dobben, van H.F.; Wamelink, G.W.W.; Braak, ter C.J.F.

    2001-01-01

    A study was conducted to determine the joint effect of gaseous atmospheric pollutants and trace elements on epiphytic lichens. We used our data to test the hypothesis that lichens are generally insensitive to toxic effects of trace elements, and can therefore be used as accumulator organisms to

  16. Comparison of trace element contamination levels (Cu, Zn, Fe, Cd ...

    African Journals Online (AJOL)

    SERVER

    2008-03-18

    Mar 18, 2008 ... Chemical analysis of the trace elements in the soft tissues. The trace elements of interest (Cu, Zn, Fe, Pb, Cd) were then determined in the digested solutions, using Thermoelemental type. M6 brand of an atomic absorption Spectrometer equipped with a flame operated atomisation system and a deuterium ...

  17. Probing Trace-elements in Bitumen by Neutron Activation Analysis

    NARCIS (Netherlands)

    Nahar, S.N.; Schmets, A.J.M.; Scarpas, Athanasios

    Trace elements and their concentrations play an important role in both chemical and physical properties of bitumen. Instrumental Neutron Activation Analysis (INAA) has been applied to determine the concentration of trace elements in bitumen. This method requires irradiation of the material with

  18. Application of K0-NAA in the Determination of Gold and other Trace Elements in Mineralized Rocks from El-Sid Gold District, Eastern Desert, Egypt

    International Nuclear Information System (INIS)

    El Abd, A.; Hamdy, M.; Mostafa, M.; El-Amir, M.

    2009-01-01

    K 0 - neutron activation analysis is an important method for multi-element analysis . The NAA k - 0 was used to determine the concentration of gold and some other trace elements in the mineralized mafic (gabro) and ultramafic (serpentinite) rocks from El-Sid gold district, Central Eastern Desert, Egypt . The samples were properly prepared together with the standards Au, Zr and Ni and simultaneously irradiated in the irradiation position 2, which is characterized with the neutron spectrum parameters a = -0.01 and f =20. After activation, the samples were subjected to gamma-ray spectrometry, using a high-purity germanium detection system and computerized multichannel analyzer. The concentrations of 25 elements, beside gold were determined. The results showed that the concentrations of incompatible elements including rare earth elements, large-ion lithophile elements (Rb, Sr, Th, Ba, Cs and Na) and high field strength elements (Ta, Hf and Zr), and the compatible elements (transition elements Co and Cr) are different from one sample to another. The results were briefly discussed within the text of this research work.

  19. Worldwide Open Proficiency Test for X Ray Fluorescence Laboratories PTXRFIAEA09: Determination of Major, Minor and Trace Elements in a River Clay

    International Nuclear Information System (INIS)

    2014-01-01

    This publication presents the results of the worldwide proficiency test PTXRFIAEA09 on the determination of major, minor and trace elements in river clay. Methodologies, a data evaluation approach, a summary evaluation of each element and individual evaluation reports for each laboratory are also described. The test was carried out within the IAEA project Nuclear Spectrometry for Analytical Applications, under the Nuclear Science Programme. The main objective of the project was to enhance the capability of interest Member States in effective utilization of nuclear spectrometries and analytical services in industry, human health and agriculture, and in monitoring and evaluating environmental pollution

  20. The Role of Trace Elements in Tinnitus.

    Science.gov (United States)

    Yaşar, Mehmet; Şahin, Mehmet İlhan; Karakükçü, Çiğdem; Güneri, Erhan; Doğan, Murat; Sağıt, Mustafa

    2017-03-01

    In this study, we aimed to investigate the role of three trace elements, namely, zinc, copper, and lead, in tinnitus by analyzing the serum level of copper and lead and both the serum and tissue level of zinc. Eighty patients, who applied to outpatient otolaryngology clinic with the complaints of having tinnitus, and 28 healthy volunteers were included. High-frequency audiometry was performed, and participants who had hearing loss according to the pure tone average were excluded; tinnitus frequency and loudness were determined and tinnitus reaction questionnaire scores were obtained from the patients. Of all the participants, serum zinc, copper, and lead values were measured; moreover, zinc levels were examined in hair samples. The levels of trace elements were compared between tinnitus and control groups. The level of copper was found to be significantly lower in the tinnitus group (p = 0.02), but there was no significant difference between the groups in terms of the levels of zinc, neither in serum nor in hair, and lead in serum (p > 0.05). The lack of trace elements, especially that of "zinc," have been doubted for the etiopathogenesis of tinnitus in the literature; however, we only found copper levels to be low in patients having tinnitus.

  1. Remediation using trace element humate surfactant

    Energy Technology Data Exchange (ETDEWEB)

    Riddle, Catherine Lynn; Taylor, Steven Cheney; Bruhn, Debra Fox

    2016-08-30

    A method of remediation at a remediation site having one or more undesirable conditions in which one or more soil characteristics, preferably soil pH and/or elemental concentrations, are measured at a remediation site. A trace element humate surfactant composition is prepared comprising a humate solution, element solution and at least one surfactant. The prepared trace element humate surfactant composition is then dispensed onto the remediation site whereby the trace element humate surfactant composition will reduce the amount of undesirable compounds by promoting growth of native species activity. By promoting native species activity, remediation occurs quickly and environmental impact is minimal.

  2. Trace Element Determination and Cardioprotection of Terminalia pallida Fruit Ethanolic Extract in Isoproterenol Induced Myocardial Infarcted Rats by ICP-MS.

    Science.gov (United States)

    Althaf Hussain, Shaik; Kareem, Mohammed Abdul; Rasool, Shaik Nayab; Al Omar, Suliman Yousef; Saleh, Alwasel; Al-Fwuaires, Manal Abdulrahman; Daddam, Jayasimha Rayalu; Devi, Kodidhela Lakshmi

    2018-01-01

    The trace elements and minerals in Terminalia pallida fruit ethanolic extract (TpFE) were determined by the instrument inductively coupled plasma-mass spectrometry (ICP-MS), and the cardioprotection of TpFE against isoproterenol (ISO)-administered rats was studied. Rats were pretreated with TpFE (100, 300, and 500 mg/kg bw) for 30 days, with concurrent administration of ISO (85 mg/kg bw) for two consecutive days. The levels of trace elements and minerals in TpFE were below the permitted limits of World Health Organization standards. ISO administration significantly increased the heart weight and cardiac marker enzymes in serum, xanthine oxidase, sodium, and calcium in the heart, whereas significantly decreased body weight, reduced glutathione, glutathione-S-transferase, superoxide dismutase, and potassium in the heart. Oral pretreatment of TpFE significantly prevented the ISO-induced alterations. This is the first report that revealed the determination of trace elements and mineral nutrients of TpFE by ICP-MS which plays a principal role in the herbal drug discovery for the treatment of cardiovascular diseases.

  3. Direct determination of trace rare earth elements in ancient porcelain samples with slurry sampling electrothermal vaporization inductively coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    Xiang Guoqiang; Jiang Zucheng; He Man; Hu Bin

    2005-01-01

    A method for the direct determination of trace rare earth elements in ancient porcelain samples by slurry sampling fluorinating electrothermal vaporization inductively coupled plasma mass spectrometry was developed with the use of polytetrafluoroethylene as fluorinating reagent. It was found that Si, as a main matrix element in ancient porcelain sample, could be mostly removed at the ashing temperature of 1200 deg. C without considerable losses of the analytes. However, the chemical composition of ancient porcelain sample is very complicated, which makes the influences resulting from other matrix elements not be ignored. Therefore, the matrix effect of ancient porcelain sample was also investigated, and it was found that the matrix effect is obvious when the matrix concentration was larger than 0.8 g l -1 . The study results of particle size effect indicated that when the sample particle size was less than 0.057 mm, the particle size effect is negligible. Under the optimized operation conditions, the detection limits for rare earth elements by fluorinating electrothermal vaporization inductively coupled plasma mass spectrometry were 0.7 ng g -1 (Eu)-33.3 ng g -1 (Nd) with the precisions of 4.1% (Yb)-10% (La) (c = 1 μg l -1 , n = 9). The proposed method was used to directly determine the trace rare earth elements in ancient porcelain samples produced in different dynasty (Sui, Ming and Qing), and the analytical results are satisfactory

  4. Trace element determination in seawater by ICP-SFMS coupled with a microflow nebulization/desolvation system

    International Nuclear Information System (INIS)

    Turetta, Clara; Cozzi, Giulio; Barbante, Carlo; Capodaglio, Gabriele; Cescon, Paolo

    2004-01-01

    Direct and simultaneous determination of Al, Ag, As, Cd, Co, Cr, Cu, Fe, Mn, Mo, Pb, Sb, U, V and Zn in diluted (1:10 v:v) seawater from the Antarctic Ocean and the Venice Lagoon at the ng mL -1 and pg mL -1 level has been performed by using an inductively coupled plasma sector field mass spectrometer (ICP-SFMS). Samples were analysed by using a PFA microflow nebulizer coupled with a desolvation system or a PFA microflow nebulizer coupled with a Teflon spray chamber, respectively. Measurements were carried out at low (LR, m/Δm=300), medium (MR, m/Δm=3,000) and high (HR, m/Δm=7,500) resolutions depending on the studied isotope. To avoid contamination, sample pre-treatment was carried out in a clean laboratory equipped with a Class 100 vertical laminar flow hood. Concentration ranges (minimum-maximum in ng mL -1 ) found in the Antarctic seawater samples (in depth profiles) were: Ag 0.0004-0.0018, As 0.69-1.32, Cd 0.031-0.096, Co 0.018-0.065, Cr 0.18-0.46, Cu 0.04-1.58, Fe 0.13-1.63, Mn 0.02-0.12, Mo 5.97-12.46, Pb 0.007-0.074, Sb 0.033-0.088, U 0.5-1.9, V 0.6-2.5 and Zn 0.16-0.80. Concentration ranges (min-max in ng mL -1 ) found in the Venice Lagoon water samples (temporal profile from a benthic chamber experiment) were: Al 0.24-0.61, Ag 0.007-0.031, As 1.42-2.27, Cd 0.050-0.182, Co 0.440-1.461, Cr 0.15-0.34, Cu 0.81-2.46, Fe 0.25-1.66, Mn 11.6-31.7, Mo 6.50-10.6, Pb 0.047-0.225, Sb 0.240-0.492, U 1.7-3.3, V 1.3-2.8 and Zn 5.20-21.5. The detection limits range between 0.06 pg mL -1 for Ag and U to 15 pg mL -1 for Fe. In order to check the accuracy of the analytical procedure, measurements of the trace elements in a certified reference material (coastal Atlantic seawater, CASS-4-NRCC) were compared with the certified values. In addition, the results from the Antarctic and Venice Lagoon samples were compared with those obtained by using different analytical techniques. (orig.)

  5. Investigation of trace elements in coal

    International Nuclear Information System (INIS)

    Gluskoter, H.J.; Cahil, R.A.; Miller, W.G.; Ruch, R.R.; Shimp, N.F.

    1976-01-01

    A variety of coal samples is currently being extensively analyzed for constituents, including many trace elements, at the Illinois State Geological Survey. The samples include whole coals, washed coals, and bench samples. Among the many determinations made on each sample are analyses for approximately 60 elements, almost twice the number of elements previously determined. The increase is in part the result of the addition of instrumental neutron activation analysis (INAA) equipment to the laboratory. Twenty-five samples of Herrin (No. 6) Coal that had been analyzed previously were subjected to INAA analysis and were found to include Ba, Ce, Cs, Dy, Eu, Au, Hf, I, In, La, Lu, Rb, Sm, Sc, Ag, Sr, Ta, Tb, Th, W, U, and Yb, none of which were reported by previous techniques. These elements generally are present in very small amounts and, with the exception of barium, exhibit no wide range in concentration. The rare earth elements are among those having the narrowest ranges. Wide variations in element content have been observed in bench sets of coals (samples of vertical segments of the coal seam). Many elements, notably germanium, are concentrated at the top and/or bottom of the seam, the high concentrations of Ge being found there in all four bench sets analyzed to date

  6. Trace element metabolism in man and animals

    International Nuclear Information System (INIS)

    Kirchgessner, M.

    1977-01-01

    Uptake, distribution, storage, excretion of different trace elements and resulting disturbances are investigated in blood and organs in animal experiments and in human diagnostics with the aid of radioisotopes. Apart from this, untritional disturbances are mentioned. Finally, future aspects of physiological trace element examinations are listed. (AJ) 891 AJ [de

  7. Trace elements as paradigms of developmental neurotoxicants

    DEFF Research Database (Denmark)

    Grandjean, Philippe; Herz, Katherine T

    2015-01-01

    Trace elements have contributed unique insights into developmental neurotoxicity and serve as paradigms for such adverse effects. Many trace elements are retained in the body for long periods and can be easily measured to assess exposure by inexpensive analytical methods that became available...

  8. Determination of trace element concentrations and stable lead, uranium and thorium isotope ratios by quadrupole-ICP-MS in NORM and NORM-polluted sample leachates

    Energy Technology Data Exchange (ETDEWEB)

    Mas, J.L., E-mail: ppmasb@us.es [Dpto. Fisica Aplicada I, EPS, Universidad de Sevilla, 41012 Sevilla (Spain); Villa, M. [Servicio de Radioisotopos, Centro de Investigacion, Tecnologia e Innovacion (CITIUS), Universidad de Sevilla, Avda. Reina Mercedes 4b, 41012 Sevilla (Spain); Dpto. Fisica Aplicada II, ETS de Arquitectura, Universidad de Sevilla, Avda. Reina Mercedes 2, 41012 Sevilla (Spain); Hurtado, S. [Servicio de Radioisotopos, Centro de Investigacion, Tecnologia e Innovacion (CITIUS), Universidad de Sevilla, Avda. Reina Mercedes 4b, 41012 Sevilla (Spain); Garcia-Tenorio, R. [Dpto. Fisica Aplicada II, ETS de Arquitectura, Universidad de Sevilla, Avda. Reina Mercedes 2, 41012 Sevilla (Spain)

    2012-02-29

    Highlights: Black-Right-Pointing-Pointer Polluted sediment and NORM samples. Black-Right-Pointing-Pointer An efficient yet fast process allowing multi-parametric determinations in <3 days. Black-Right-Pointing-Pointer Trace element concentrations, Pb, Th and U isotope ratios with a single instrument. - Abstract: This work focuses on the monitoring of the potential pollution in scenarios that involve NORM-related industrial activities (environmental or in-door scenarios). The objective was to develop a method to determine extent and origin of the contamination, suitable for monitoring (i.e. simple, fast and economical) and avoiding the use of too many different instruments. It is presented a radiochemical method that allows the determination of trace element concentrations and {sup 206}Pb/{sup 207}Pb/{sup 208}Pb, {sup 238}U/{sup 234}U and {sup 232}Th/{sup 230}Th isotope ratios using a single sample aliquot and a single instrument (ICP-QMS). Eichrom UTEVA{sup Registered-Sign} extraction chromatography minicolumns were used to separate uranium and thorium in sample leachates. Independent ICP-MS determinations of uranium and thorium isotope ratios were carried out afterwards. Previously a small aliquot of the leachate was used for the determination of trace element concentrations and lead isotope ratios. Several radiochemical arrangements were tested to get maximum performances and simplicity of the method. The performances of the method were studied in terms of chemical yields of uranium and thorium and removal of the potentially interfering elements. The established method was applied to samples from a chemical industry and sediments collected in a NORM-polluted scenario. The results obtained from our method allowed us to infer not only the extent, but also the sources of the contamination in the area.

  9. Application of NAA to the determination of mineral and trace elements in Brazilian diets at IPEN/CNEN/SP

    International Nuclear Information System (INIS)

    Favaro, D.I.T.; Maihara, V.A.; Souza, S.A.; Vasconcellos, M.B.A.; Mafra, D.; Cordeiro, M.B.C.; Cozzolino, S.M.F.

    2000-01-01

    Concentration of the 14 elements Br, Ca, Cl, Co, Cs, Fe, K, Mn, Na, Rb, Sc, Se and Zn have been determined by INAA in diets of four different groups: (a) 19 pre-school children, (b) 18 healthy adults, (c) 23 elderly people living in private institutions and (d) 19 patients with chronic renal failure (CRF). The contents of proteins, lipids and carbohydrates were also analysed in the diets. The daily intakes of the elements analysed were compared to the recommended values set by RDA or WHO. (author)

  10. Trace element fingerprinting of emeralds by PIXE/PIGE

    International Nuclear Information System (INIS)

    Ma Xinpei; MacArthur, J.D.; Roeder, P.L.; Mariano, A.N.

    1993-01-01

    Gemologists consider the mineral beryl, beryllium aluminium silicate, to be the gem, emerald, when it contains sufficient chromium, >0.1%, to colour it a strong green. Emeralds usually contain other trace elements. To investigate the feasibility of distinguishing an emerald's country of origin through its trace content, the trace elements in emeralds and a few beryls from sixteen locations have been determined with a single nondestructive measurement using PIXE and PIGE. From the database established with this limited number of samples, distinguishing trace element patterns were found. (orig.)

  11. Neutron activation analysis determination of trace elements in suspended particulate material and in central Thyrrenian sea sediments

    International Nuclear Information System (INIS)

    Madaro, M.; Moauro, R.; Boniforti, R.

    1985-01-01

    Neutron activation analysis and gamma-spectrometry have been applied to the instrumental determination of 26 elements (As, Au, Ca, Ce, Co, Cr, Cs, Eu, Fe, Hf, Hg, La, Lu, Mn, Rb, Sb, Sc, Se, Sm, Ta, Tb, Th, W, Yb, Zn, Zr) in samples of suspended particulate matter and sediments collected in the stretch of Tyrrhenian Sea between the Volturno River mouth and the Cape of Circeo. Some of these elements have particular importance because they can be toxic to the organisms or can be used as tracers in the aquatic environment of radioisotopes generated in activation or fission processes. Results show that some elements, not constituting particular crystal lattices, are more concentrated in particulate matter than in sediments. Such results agree with the hypothesis, supported also by others, that particulate matter acts as a scavenger with respect to most microelements, because of both biological and physico-chemical phenomena

  12. Determination of trace elements in freshwater rotifers and ciliates by total reflection X-ray fluorescence spectrometry

    Science.gov (United States)

    Woelfl, S.; Óvári, M.; Nimptsch, J.; Neu, T. R.; Mages, M.

    2016-02-01

    Element determination in plankton is important for the assessment of metal contamination of aquatic environments. Until recently, it has been difficult to determine elemental content in rotifers or ciliates derived from natural plankton samples because of the difficulty in handling and separation of these fragile organisms. The aim of this study was to evaluate methods for separation of rotifers and large ciliates from natural plankton samples (μg range dry weight) and subsequent analysis of their elemental content using total-reflection X-ray fluorescence spectrometry (TXRF). Plankton samples were collected from different aquatic environments (three lakes, one river) in Chile, Argentina and Hungary. From one to eighty specimens of five rotifer species (Brachionus calyciflorus, Brachionus falcatus, Asplanchna sieboldii, Asplanchna sp., Philodina sp.) and four to twelve specimens of one large ciliate (Stentor amethystinus) were prepared according to the dry method originally developed for microcrustaceans, and analysed by TRXF following in situ microdigestion. Our results demonstrated that it possible to process these small and fragile organisms (individual dry mass: 0.17-9.39 μg ind- 1) via careful washing and preparation procedures. We found species-dependent differences of the element mass fractions for some of the elements studied (Cr, Mn, Fe, Ni, Cu, Zn, As, Pb), especially for Cu, Fe and Mn. One large rotifer species (A. sieboldii) also showed a negative correlation between individual dry weight and the element content for Pb, Ni and Cr. We conclude that our application of the in situ microdigestion-TRXF method is suitable even for rotifers and ciliates, greatly expanding the possibilities for use of plankton in biomonitoring of metal contamination in aquatic environments.

  13. Multielemental determination of trace elements in radiopharmaceuticals produced at the radiopharmacy center using ICP-OES technique

    International Nuclear Information System (INIS)

    Tavares, Angelica T.; Martins, Patricia de A.; Fukumori, Neuza T.O.; Mengatti, Jair; Matsuda, Margareth M.N.

    2013-01-01

    The control of chemical impurities in radiopharmaceuticals is critical to their safety and efficacy. According to the U.S. Pharmacopeia (USP), the elemental impurities with potential toxicity must be quantified. A proposed revision of USP 35 introduces the technique of atomic emission spectrometry for the analysis of elements. The aim of this work was to study the concentration of chemicals elements in FDG-Fluor-18, IPEN-TEC Generator and MIBI-TEC using an ICP-OES technique. One analytical curve composed by 27 elements (Ag, A1, B, Ba, Be, Bi, Ca, Cd, Co, Cr, Cu, Fe, Ga, K, Li, Mg, Mn, Mo, Na, Ni, Pb, Pd, Se, Sr, Te, T1, Zn) was constructed in two analytical ranges. The analyses were carried out simultaneously in an ICP-OES Vista MPX (Agilent). Some parameters for analysis and method validation were evaluated. The cleaning and maintenance of equipment influenced the emission intensity of the elements. 1.2 power and 10s sample uptake resulted in a consumption of 1.6 mL of sample and Mg II/Mg I ratio relation equal to 9.40. Linearity, LOD and LOQ were determined. The analysis were performed using 1:40 dilution with purified water. The main elements studied in this work were A1, Cu and Zn. The % recovery was determined with final concentrations of 0.3, 0.5 and 0.8 μg mL -1 . The analyses were performed in triplicate with three different batches. The % recovery was between 96.65 and 117.61% and the values for precision (CV) were less than 5% indicating good accuracy of the method. (author)

  14. Determination of rare-earths and other trace elements in neo proterozoic-neo paleozoic dykes from Ceara state, Brazil, by neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Anjos, Rafael Martins dos; Figueiredo, Ana M.G., E-mail: rafael.anjos@usp.b, E-mail: anamaria@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro do Reator Nuclear de Pesquisas. Lab. de Analise por Ativacao com Neutrons; Cardoso, Gustavo Luan; Marques, Leila S., E-mail: leila@iag.usp.b [Universidade de Sao Paulo (IAG/USP), SP (Brazil). Inst. de Astronomia, Geofisica e Ciencias Atmosfericas

    2011-07-01

    Trace elements such as rare earths, U, Th, Ta, Ba and Hf can be very useful in petrogenetic studies of igneous and metamorphic rocks, giving information about the origin and evolution of magmas. Instrumental Neutron Activation Analysis (INAA) is an accurate and precise for trace element analysis in geological samples, and provides the information required for this kind of studies. In this study, rare earths and incompatible trace elements were determined by INAA in the geological reference materials GS-N and BE-N, to quality control, and for the investigation of acid dykes of neo proterozoic-neo paleozoic ages, which outcrop in the Medio Coreau and Ceara Central domains from the Borborema Province (Ceara State). The powdered samples (particle sizes less than 100 mesh), crushed by using a mechanical agate mortar grinder, were irradiated at the IEA-R1 nuclear reactor at IPEN-CNEN/SP, and the induced activity was measured by high resolution gamma-ray spectrometry. The accuracy and precision of the method were evaluated and preliminary results of dyke samples are presented. (author)

  15. The use of a chelating resin column for preconcentration of trace elements from sea-water in their determination by neutron-activation analysis

    International Nuclear Information System (INIS)

    Lee, C.; Kim, N.B.; Lee, I.C.; Chung, K.S.

    1977-01-01

    A Chelex-100 resin column has been employed for the preliminary concentration of trace elements in water samples before their determination by neutron-activation analysis. The column filled with a 1 : 1 mixture of the resin (50 to 100 mesh) and Pyrex glass powder of the same mesh size, is shown to maintain a constant flow-rate and give reproducible results. By a combination of preconcentration and neutron-activation analysis it is possible to determine Ba, Ca, Cd, Ce, Co, Cr, Cu, Fe, La, Mg, Mn, Sc, U, V and Zn in sea-water and/or fresh water simultaneously at the parts per milliard level. (author)

  16. Determination of k0-factors of short-lived nuclides and application of k0-NAA to selected trace elements

    International Nuclear Information System (INIS)

    Acharya, R.; Holzbecher, J.; Chatt, A.

    2012-01-01

    As part of the standardization program of k 0 -based NAA (k 0 -NAA) methods at the Dalhousie University SLOWPOKE-2 reactor (DUSR) facility, the k 0 -factors of 15 analytically important short-lived nuclides (half-life 197 Au). The elemental standards used were prepared mostly from their primary standard solutions. The samples were irradiated in both inner and outer pneumatic sites of the DUSR facility and counted using an HPGe-detector coupled to an ORTEC’s digital gamma-ray spectrometer. The k 0 -factors determined using both inner and outer irradiation sites were found to be within ±5% with respect to either recommended or literature values in most cases. The Z-score values at 95% confidence level were found to be in the range of ±0.03–1.6. The k 0 -NAA method was applied to three different NIST standard reference materials (SRMs) and concentrations of six elements, namely Ag, F, Hf, Rb, Sc, and Se were determined using their short-lived nuclides. The concentrations of these elements were also determined by relative NAA method for comparison purposes.

  17. Determination of trace elements in Brazilian rice grains and in biological reference materials by neutron activation analysis

    International Nuclear Information System (INIS)

    Maihara, V.A.; Vasconcellos, M.B.A.

    1989-01-01

    Instrumental neutron activation analysis was applied to the determination of the elements Na, K, Br, As, Rb, Zn, Co, Fe and Sc in Brazilian rice samples and in biological standards. Hg and Se concentrations were determined by using a simple radiochemical separation. The chemical procedure was carried out by means of distillation of Hg and Se in HBr medium and subsequent precipitation of selenium by sodium methabissulfide and mercury by thioacetamide. The accuracy of the instrumental and radiochemical methods was evaluated by means of analysis of the Reference Materials NBS-Bovine Liver, Bowen's Kale and NBS-Rice Flour. (author) [pt

  18. Determination of trace elements in Brazilian rice grains and in biological reference materials by neutron activation analysis

    International Nuclear Information System (INIS)

    Maihara, V.A.; Vasconcellos, M.B.A.

    1989-01-01

    INAA was applied to the determination of the elements Na, K, Br, As, Rb, Zn, Co, Fe and Sc in Brazilian rice samples and in biological standards. Hg and Se concentrations were determined using a simple radiochemical separation. The chemical procedure was carried out by means of distillation of Hg and Se in HBr medium and subsequent precipitation of Se by sodium metabisulfite and Hg by thioacetamide. The accuracy of the instrumental and radiochemical methods was evaluated by means of analysis of the Reference Materials NBS-Bovine Liver, Bowen's Kale and NBS-Rice Flour. (author) 15 refs.; 5 tabs

  19. Network application of PIXE trace element analysis

    International Nuclear Information System (INIS)

    Niizeki, T.; Kawasaki, K.; Hattori, T.

    2003-01-01

    Particle Induced X-ray Emission (PIXE) is a very sensitive analytical technique for determinations of trace elements. But the number of users is limited because there are not so much accelerators which can be used easily. On the other hand, PIXE is a typical machine analysis which can easily analyze automatically and make online data acquisition system. If there is useful online data handling system then PIXE analysis should be more useful for many persons. Therefore we develop to online PIXE facility at Tokyo Institute of Technology VdG laboratory and use it for environmental educations. (author)

  20. Trace element concentrations in higher fungi

    International Nuclear Information System (INIS)

    Byrne, A.R.; Ravnik, V.; Kosta, L.

    1976-01-01

    The concentrations of ten trace elements, As, Br, Cd, Cu, Hg, I, Mn, Se, Zn and V, have been determined in up to 27 species of higher fungi from several sites in Slovenia, Yugoslavia. Analyses were based on destructive neutron activation techniques. Data are presented and compared with the concentrations found in soils. Previously values were non-existent or scanty for these elements, so that the data represent typical levels for basidiomycetes. In addition to confirming high levels of mercury in many species, the survey also found that cadmium is accumulated to a surprising extent by most fungi, the average value being 5 ppm. Among other accumulations found was bromine by the genus Amanita, and selenium by edible Boletus. Correlation analysis between all pairs of trace elements gave values for r of from 0.75 to 0.43 for 7 pairs (Cu and Hg, 0.75; Se and As, 0.69). As well as these features of biochemical interest, the values found and the pattern of accumulation suggest potential uses of fungi in environmental studies

  1. Determination of trace elements in some fruits collected in Vietnam and Korea by neutron activation analysis on Dalat and HANARO research reactors

    International Nuclear Information System (INIS)

    Nguyen Thi Sy; Ho Manh Dung; Ho Van Doanh; Tran Quang Thien; Chung Yong-Sam

    2015-01-01

    The k_0-based neutron activation analysis (k_0-NAA) has been applied for determination of trace multi-element in 5 fruits: orange, tomato, persimmon, pear and apple. The samples were collected in Vietnam and Korea, and dried-frozen in laboratory at a temperature of -65"oC, weighed approximately 50 mg or 100 mg each sample, and put in clean polyethylene bags for short and long time irradiations, respectively. The NIST-1547 (Peach Leaves) and IAEA-V-10 (Hay Powder) were used for the purpose of quality control. Both analytical and standard samples were irradiated in the 500 kW Dalat research reactor (Vietnam) and the 20 MW HANARO research reactor (Korea). Concentration of 16 elements: Al, As, Au, Br, Ca, Cl, Co, Eu, Fe, K, La, Mg, Mn, Na, Rb and Zn were determined. By comparison the concentrations of trace elements in the investigated Vietnam and Korea fruits, revealed that they are mostly similar between two places. However, the Ca concentration in orange from Vietnam was approximately 2.5 times higher than that one from Korea, whereas the Ca concentration in pear from Vietnam was approximately 21 times lower than that one from Korea. The Mn concentrations in all of fruits that collected in Vietnam were mostly higher than those collected in Korea, ranging between 1.4 to 2.2 times. (author)

  2. Determination of radioactive trace elements in ashes and fly-ashes from Brazilian coal-fired power plants

    International Nuclear Information System (INIS)

    Bellido, L.F.; de Castro Arezzo, B.

    1984-01-01

    The aim of this work was to apply a epithermal neutron activation technique to determine the uranium and thorium content in coal ashes and fly ashes from Brazilian coal-fired thermoelectric plants and to evaluate the contribution of these elements and their descendents to the environmental radioactivity. Brazil has adopted as short term policy the use of alcohol and coal as alternative sources of energy. With regard to coal, large deposits of this mineral are found in southern states but the serious problem of its utilization is the risk of environmental contamination which can reach dangerous levels because the industrial plants burn several million tons per year. Uranium and thorium contents, determined experimentally, are extrapolated for annual coal consumption and their amounts and the activity of the radium isotopes descendents released to the atmosphere are calculated. The significance of these values and problems in environmental pollution are discussed

  3. Recent developments in automated determinations of trace level concentrations of elements and on-line fractionations schemes exploiting the micro-sequential injection - lab-on-valve approach

    DEFF Research Database (Denmark)

    Hansen, Elo Harald; Miró, Manuel; Long, Xiangbao

    2006-01-01

    The determination of trace level concentrations of elements, such as metal species, in complex matrices by atomic absorption or emission spectrometric methods often require appropriate pretreatments comprising separation of the analyte from interfering constituents and analyte preconcentration...... are presented as based on the exploitation of micro-sequential injection (μSI-LOV) using hydrophobic as well as hydrophilic bead materials. The examples given comprise the presentation of a universal approach for SPE-assays, front-end speciation of Cr(III) and Cr(VI) in a fully automated and enclosed set...

  4. Trace elements in coloured opals using neutron activation analysis

    International Nuclear Information System (INIS)

    McOrist, G.D.; Smallwood, A.

    1995-01-01

    Neutron activation analysis was used to determine the concentration of trace elements in 50 samples of orange, yellow, honey, green, blue and pink opals as well as 18 samples of colourless opals taken from a number of recognised fields in Australia, Peru, Mexico and USA. The results were evaluated to determine the relationship between trace elements content and opal colour. (author). 10 refs., 10 figs., 3 tabs

  5. Toxic trace elements in Chilean seafoods

    International Nuclear Information System (INIS)

    De Gregori, I.; Delgado, D.; Pinochet, H.; Gras, N.; Thieck, M.; Munoz, L.; Bruhn, C.; Navarrete, G.

    1992-01-01

    Chile is a well known producer and exporter of shell fish. These seafoods, like other specimens of marine origin, are susceptible to environmental and other contaminations like trace elements, including toxicants. Therefore adequate analytical quality assurance is mandatory before accepting analytical results. In this context, use of at least 2 independent methods of determination and validation with certified reference materials (CRM) provides acceptable criteria for judging the reliability of the data. This paper describes sample treatments and analytical procedures for Cd, Cu and Hg determinations in mollusc samples. Three independent analytical techniques, namely differential pulse anodic stripping voltammetry, neutron activation analysis and atomic absorption spectrometry, were used. CRM standards of the IAEA, NIST and BCR were analyzed to evaluate quality assurance. Following the quality control phase, the concentrations of cadmium, copper, and mercury in fresh and canned mollusc samples Tagelus dombeii and Semelle solida (Navajuelas and Almejas chilenas respectively) from different locations were determined. (author). 32 refs.; 4 figs.; 7 tabs

  6. Development of a quantitative method for trace elements determination in ores by XRF: an application to phosphorite from Olinda (PE), Brazil

    International Nuclear Information System (INIS)

    Imakuma, K.; Sato, I.M.; Cretella Neto, J.; Costa, M.I.

    1976-01-01

    A quantitative analytical method by means of X-Ray Fluorescence intended to determine Zn, Cu and Ni trace amounts in a phosphorite ore from Olinda, PE-Brazil was established. The double dilution method with borax as the melting flux was the one choosed because ores diluted in borax in the form of melted samples show matrix effects with respect to the element to be analysed; it was possible to identify the elements already presented in the ore that caused interference in the Zn, Cu and Ni determinations. Such elements were Ca and their quantities were subsequently determined. The addition of appropriate quantities of Fe and Ca to standards allowed us to minimize the matrix effects without the undersired introduction of extraneous elements in the ore, moreover, the urge of knowing the exact amounts of Fe and Cu present in the ore drove us towards a simultaneous development of another analytical method suitable to measure medium to high contents. This method also made use of the technique of dilution with melting. These methods present advantages such as: a quantitative analysis with great reproducibility of results; the extension of the method to routine determination, to all kinds of ores. The main sources of error can be controlled, allowing an accuracy as high as +- 1 ppm for Cu, +- 4 ppm for Ni, +- 6 ppm for Zn and +- 1% for both Fe can Ca under the most unfavorable conditions

  7. Trace element analysis of nail polishes

    International Nuclear Information System (INIS)

    Misra, G.; Mittal, V.K.; Sahota, H.S.

    1999-01-01

    Instrumental neutron activation analysis (INAA) technique was used to measure the concentrations of various trace elements in nail polishes of popular Indian and foreign brands. The aim of the present experiment was to see whether trace elements could distinguish nail polishes of different Indian and foreign brands from forensic point of view. It was found that cesium can act as a marker to differentiate foreign and Indian brands. (author)

  8. The determination of trace elements in commercial human serum albumin solutions by proton-induced X-ray emission spectrometry and neutron activation analysis

    International Nuclear Information System (INIS)

    Maenhaut, W.; De Reu, L.; Tomza, U.; Versieck, J.

    1982-01-01

    Particle induced X-ray emission (p.i.x.e.) and neutron activation analysis (n.a.a.) are proposed for determining the trace element content of human serum albumin. Application of these methods to some commercial albumin solutions provided concentration data for up to 19 elements, most of which were present at a level below a few μg ml -1 . The precision of the p.i.x.e. technique, as determined by irradiating up to 20 targets from one sample, was about 3% for those elements where counting statistics were good. A comparison between the p.i.x.e. and n.a.a. results showed close agreement, indicating that p.i.x.e. can yield data which are accurate to within 10%. Neutron activation showed very good sensitivity for the elements producing long-lived nuclides (tsub(1/2) >= 3 days), but had rather high detection limits for the other elements, unless radiochemical separations were used. (Auth.)

  9. Heavy metals and related trace elements

    International Nuclear Information System (INIS)

    Leland, H.V.; Luoma, S.N.; Wilkes, D.J.

    1977-01-01

    A review is given of heavy metals and related trace elements in the aquatic environment. Other reviews and bibliographies are cited, dealing with the metabolism and transport of metal ions and with the toxic effects of stable and radioactive trace metals on aquatic organisms. The sources of trace elements in natural waters are discussed. It is suggested that atmospheric inputs of several trace metals comprise sizable fractions of total inputs to the Great Lakes and continental shelf waters. Information on stack emissions of trace elements from a coal-fired steam plant was used to estimate the likely range of air concentrations and inputs to a forested watershed in Tennessee. Some basic concepts of cycling of elements through aquatic communities were examined, such as the Pb, Mn and Zn concentrations in sediment and estuarine plants and animals colonizing dredge-spoil disposal areas. The use of plants as biological indicators of trace element contamination was outlined, as well as bioaccumulation in aquatic fauna. The effects of environmental factors on the kinetics of element exchange were noted, for example the influx rates of Cs 137 in tubificid worms, and Co 60 and Zn 65 in shrimp were shown to be temperature dependent. The toxicity of heavy metals on aquatic fauna was discussed, such as the histopathological lesions in the kidney and liver of fishes caused by heavy metals, and the effects of Hg and Cu on the olfactory response of rainbow trout

  10. Determination of trace elements in human liver biopsy samples by ICP-MS and TXRF: hepatic steatosis and nickel accumulation

    Energy Technology Data Exchange (ETDEWEB)

    Varga, Imre; Szoboszlai, Norbert [L. Eoetvoes University, Department of Inorganic and Analytical Chemistry, P.O. Box 32, Budapest (Hungary); Szebeni, Agnes [MI Central Hospital, Ultrasound Laboratory, Budapest (Hungary); Kovacs, Bela [Debrecen University - Centre of Agricultural Sciences, Department of Food Science and Quality Assurance, P.O. Box 36, Debrecen (Hungary)

    2005-10-01

    Human liver biopsy samples, collected from 52 individuals, were analysed by inductively coupled plasma-mass spectrometry (ICP-MS) and total reflection X-ray fluorescence (TXRF) spectrometry in a retrospective study (i.e. patient selection and liver biopsy were not for the purpose of element analysis). The freeze-dried samples (typically 0.5-2 mg dry weight) were digested in a laboratory microwave digestion system and solutions with a final volume of 1 mL were prepared. The concentrations of Cr, Mn, Fe, Ni, Cu, Zn, Rb, and Pb were determined by use of a Thermo Elemental X7 ICP-MS spectrometer. TXRF measurements were performed with an Atomika Extra IIA spectrometer. Yttrium was employed as an internal standard, prepared by dissolution of 5N-purity yttria (Y{sub 2}O{sub 3}) in our laboratory. The accuracy was tested by analysis of NIST 1577a Bovine Liver certified reference material. The concentrations of Fe, Cu, Zn, and Rb determined in human liver biopsy samples were in good agreement with data published by other authors. The distribution of nickel in the samples was surprisingly uneven - nickel concentrations ranged from 0.7 to 12 {mu}g g{sup -1} (dry weight) in 38 samples and in several samples were extremely high, 36-693 {mu}g g{sup -1}. Analysis of replicate procedural blanks and control measurements were performed to prevent misinterpretation of the data. For patients with steatosis (n=14) Ni concentrations were consistently high except for two who had levels close to those measured for the normal group. As far as we are aware no previous literature data are available on the association of steatosis with high concentration of nickel in human liver biopsies taken from living patients. (orig.)

  11. Determination of trace amounts of rare earth elements in samarium, terbium and disprosium oxides by graphite furnace atomic-absorption spectrometry

    International Nuclear Information System (INIS)

    Dantas, E.S.K.

    1990-01-01

    A graphite furnace atomic-absorption spectrometry method for the determination of neodymium, europium, terbium, dysprosium and yttrium at trace level in samarium oxide; of samarium, europium, dysprosium, holmium, erbium and yttrium in terbium oxide and of europium, terbium, holmium, erbium and yttrium in dysprosium oxide was established. The best pyrolysis and atomization temperatures were determined for each lanthanide considered. Calibration curves were obtained for the pure elements, for binary mixtures formed by the matrix and each of the lanthanides studied and, finally, for the complex mixtures constituted by the matrix and all the other lanthanide of the group under scrutiny. This study has been carried out to examine the interference of the presence of one lanthanide on the behaviour of the other, since a lack of linearity on the calibration curves has been observed in some cases. Detection and determination limits have been determined as well. The detection limits encountered were within the range 0.002 to 0.3% for different elements. The precision of the method expressed as the relative standard deviation was calculated for each element present in each of the matrices studied. The conclusion arrived at is that the method can be applied for determining the above mentioned lanthanides present in the matrices studied with purity up to 99.50%. (author)

  12. World-wide and regional intercomparison for the determination of trace elements in polluted marine sediment IAEA-356. Report no.56

    Energy Technology Data Exchange (ETDEWEB)

    Horvat, M; Mee, L D; Oregioni, B [International Atomic Energy Agency, Marine Environment Laboratory, Monaco (Monaco)

    1994-09-01

    The accurate and precise determination of trace elements in marine sediment samples is an important aspect of geochemical marine pollution studies and for assessing the levels and pathways of marine pollutants. Past intercomparison exercise conducted by the Marine Environment Laboratory of IAEA (formerly the International Laboratory of Marine Radioactivity) has focused upon the near shore sediment (1) and deep sea marine sediment (2) where trace levels of elements was rather low. The present intercomparison exercise on sediment taken from a polluted coastal lagoon was designed in order to fulfill the increased demand for certified reference materials of various origin and the number of parameters that should be studied. Additionally, different instrumental techniques, both nuclear and non-nuclear, were compared, and evaluated. By statistically examining the data from this study, the material can be certified for future use as a reference material. The current exercise was designed not only to test the intercomparability of different instrumental techniques, but also to evaluate the effectiveness of different procedures for sample digestion. Participants were invited to perform 'total' analyses involving, except in the case of neutron activation analysis, a simple partial extraction with 1M hydrochloric acid (2 hours, room temperature). This partial dissolution had a twofold purpose: (i) to differentiate between instrumental (plus contamination during work-up) errors and those resulting from method-specific (matrix) effects; and (ii) to evaluate a simple screening test for the more labile ('easily leached') fraction of trace elements of particular interest to environmental chemists. The present report presents the entire experimental data set and a statistical evaluation of the results for each parameter.

  13. Incorporation of trace elements into hair structure

    International Nuclear Information System (INIS)

    Limic, N.; Valkovic, V.

    1985-01-01

    Examining blood and urine provides an immense insight into human diseases. It is natural to hope that the hair studies will be added routinely to the examinations. Human head hair is a recording filament which can reflect metabolic changes of many elements over a long period of time. The idea of hair analysis is very inviting, because hair is easily samples, shipped and analyzed. In this paper the authors propose a method for the determination of some diffusion parameters from experimental data on the distribution of trace element concentrations in hair and then a method for the determination of the radial diffusion constants of Se, Zn and Pb. The authors' model of hair structure with respect to diffusion is based on the supposition of cross-sectional homogeneity as well as the longitudinal homogeneity of hair. This supposition implies nonisotropic diffusion in hair which is described by two diffusion constants. Diffusion constants can be determined by experiment on wetting hair in solvents or by measurements of natural contamination of hair in air. The first type of experiments can be arranged in various ways to separate radial diffusion from the longitudinal one and, consequently, to determine two diffusion constants from various sets of experiments. The authors' aim is to consider only radial diffusion in hair and to determine the radial diffusion constants of Se, Zn and Pb

  14. Determination of essential and trace elements in milk and measurement of short-lived nuclides using FIMS

    International Nuclear Information System (INIS)

    Demiralp, R.; Kalayoglu, S.; Unseren, E.; Grass, F.; Boeck, H.

    1988-01-01

    In the experiments, Gueluem, Sek and Pinar brand of bottled milks and Pinar milk powder which are commercially available were used. As standards IAEA Milk powder A-11, NBS-Orchard Leaves 1571 and for Cu single standard was used. Samples and standards were irradiated together in the central thimble of I.T.U. TRIGA Mark-II reactor for 1-8 hrs and for 60 sec in the fast pneumatic tube of TRIGA Reactor. Depending on the nuclear characteristics of the isotopes to be analyzed, they are counted at different counting times. The activities were measured with a high-purity Ge detector coupled to Canberra 90 model multichannel analyzer in the ITU. In order to determine short half-life nuclides a very fast irradiation and measuring system (FIMS) has been used. When the average values of the 16 elements are considered, it is observed that the amount of Na, As, Al, Mn, Zn, Rb , Co in the milk powder is greater than that of milk, where as in Pinar milk, which is a durable kind of milk, the amount of Na, K, Br, Al , As, Zn, Co is larger than that in daily milk. When daily products of different brands are compared, it was found that the quantity of Fe, Cr, Mg is higher while Cl, Sb, Zn, Rb, Co is less than that in Gueluem milk. The quantity of Cl is about 10 times as much and Mg 7 times less than in Sek milk. It was not possible to investigate how the seasons and the regions from where the milk was collected affect the quantity of the elements. It will be useful to continue the study in this field

  15. Curve resolution and figures of merit estimation for determination of trace elements in geological materials by inductively coupled plasma atomic emission spectrometry

    International Nuclear Information System (INIS)

    Lorber, A.; Harel, A.; Goldbart, Z.; Brenner, I.B.

    1987-01-01

    In geochemical analysis using inductively coupled plasma atomic emission spectrometry (ICP-AES), spectral interferences and background enhancement in response to sample concomitants are the main cause of deterioration of the limit of detection (LOD) and inaccuracy of the determination at the trace and minor element levels. In this account, the authors describe the chemometric procedure of curve resolution for compensating for these sources of error. A newly developed method for calculating figures of merit is used to evaluate the correction procedure, test the statistical significance of the determined concentration, and determine LODs for each sample. The technique involves scanning the vicinity of the spectral line of the analyte. With prior knowledge of potential spectral interferences, deconvolution of the overlapped response is possible. Analytical data for a wide range of geological standard reference materials demonstrate the effectiveness of the chemometric techniques. Separation of 0.002 nm spectral coincidence, employing a 0.02 nm resolution spectrometer, is demonstrated

  16. Determination of natural radioactive elements in building materials by gamma spectroscopy, trace dosimetry and neutron activation analysis

    International Nuclear Information System (INIS)

    Perez, G.; Desdin, L.F.; Hernandez, A.T.; Gonzalez, D.; Labrada, A.; Tenreiro, J.J.; Capote, G.; Perelyguin, V.P.; Herrera, H.; Tellez, E.

    1993-01-01

    Five types of Cuban concretes and their main components (minerals aggregates and cement) were investigated in order to analyze the content of uranium, thorium, radium, potassium and radon 220,222, using gamma spectroscopy, trace dosimetry and neutron activation analysis. The comparative evaluation of different concretes, aggregates and two types of cements according to natural radioactivity is shown

  17. Trace element determination study in human hair by neutron activation analysis; Estudo da determinacao de elementos traco em cabelos humanos pelo metodo de analise por ativacao com neutrons

    Energy Technology Data Exchange (ETDEWEB)

    Frazao, Selma Violato

    2008-07-01

    Human hair analysis studies have been subject of continuous interest due to the fact that they can be used as an important tool to evaluate trace element levels in the human body. These determinations have been carried out to use hair for environmental and occupational monitoring, to identify intoxication or poisoning by toxic metals, to assess nutritional status, to diagnose and to prevent diseases and in forensic sciences. Although hair analysis presents several advantages over other human tissue or fluid analyses, such as organ tissue, blood, urine and saliva, there are some controversies regarding the use of hair analysis data. These controversies arise from the fact that it is difficult to establish reliable reference values for trace elements in hair. The purpose of this study was to evaluate the factors that affect element concentrations in hair samples from a population considered healthy and residing in the Sao Paulo metropolitan area. The collected human head hair was cut in small pieces, washed, dried and analyzed by neutron activation analysis (NAA). Aliquots of hair samples and synthetic elemental standards were irradiated at the IEA-R1 nuclear research reactor for 16 h under a thermal neutron flux of about 5x10{sup 12} n cm{sup -2} s{sup -1} for As, Br, Ca, Co, Cr, Cs, Cu, Fe, K, La, Na, Sb, Sc, Se and Zn determinations. The induced gamma activities of the standards and samples were measured using a gamma ray spectrometer coupled to an hiperpure Ge detector. For quality control of the results, IAEA- 85 Human Hair and INCT-TL-1 Tea Leaves certified reference materials (CRMs) were analyzed. Results obtained in these CRMs presented for most of elements, good agreement with the values of the certificates (relative errors less than 10%) and good precision (variation coefficients less than 13.6%). Results of replicate hair sample analysis showed good reproducibility indicating homogeneity of the prepared sample. Results obtained in the analyses of dyed and

  18. Development and optimization of a nuclear method to determine the lead concentration as an ultra-trace element in ultra-pure water

    International Nuclear Information System (INIS)

    Amara, A.; Giovagnoli, A.; Barrandon, J.N.

    1994-01-01

    Here we intend to perfect a nuclear analytical technique for the determination of lead concentration as an ultra-trace element in ultra-pure water Inmost cases the analysis of an aqueous solution is made by non-nuclear methods, therefore methods which are sensitive to the chemical form of the element to be determined. To ovoid this problem we developed a nuclear technique using a cyclotron,which allows the determination of the lead concentration in any of its chemical forms. We studied the possibilities of several incident beams, like neutral particles and charged particles. Proton activation showed to be the most sensitive of all the irradiation procedures. Several points have though be studied and developed: - an irradiation cell for liquids irradiation under a strong proton current; - the bismuth chemical separation. This element has two radio-isotopes allowing the determination of lead;-optimize the experimental irradiation and measurements parameters in order to reach the lower detection limit. At last an intercomparison of several techniques has been made for different standards. It clearly showed that, contrary to atomic,potentiometric or mass spectrometry methods,only activation technique give accurate and reproducible results. (author).1 fig., 2 tabs., 4 refs

  19. Determination of minor, trace and toxic elements in chewing tobacco products by instrumental neutron activation analysis and identification of glutamic acid

    International Nuclear Information System (INIS)

    Garg, A.N.; Paul Choudhury, R.; Acharya, R.; Reddy, A.V.R.

    2012-01-01

    Tobacco smoking/chewing has been a cause of concern because of it being related with oral cancer. It causes stimulation and ill physiological effects. Ten different brands of spit tobacco, eight gutkaas and five paan masalas have been analyzed for seven minor (Al, Na, K, Ca, Cl, Mg, and P) and 17 trace (As, Ba, Br, Co, Cr, Cs, Cu, Eu, Fe, Hg, La, Mn, Rb, Sb, Sc, Th, and Zn) elements by instrumental neutron activation analysis. Also Ni and Pb were determined by atomic absorption spectrophotometry. Concentration of Cd was below detection limit ( -1 ) in the tobacco samples. Mg, generally added as MgCO 3 to prevent caking, is present as minor constituent in spit tobacco and gutkaas but is below detection limit ( -1 ) in paan masalas. Most elemental concentrations vary in a wide range depending on the nature of chewing tobacco. Spit tobacco has been found to be more enriched in essential elements (Ca, K, Na, P, Mn, and Rb), whereas gutkaas contain higher concentrations of Fe, Cr, Cu, and Zn. Paan masalas contain lower contents of other elements but higher content of Hg. Gutkaas also contain higher amounts of As and Pb. Further glutamic acid has been separated from tobacco leaves and characterized as it might bind with some elements. (author)

  20. Determination of toxic and essential trace elements in serum of healthy and hypothyroid respondents by ICP-MS: A chemometric approach for discrimination of hypothyroidism.

    Science.gov (United States)

    Stojsavljević, Aleksandar; Trifković, Jelena; Rasić-Milutinović, Zorica; Jovanović, Dragana; Bogdanović, Gradimir; Mutić, Jelena; Manojlović, Dragan

    2018-07-01

    Inductively coupled plasma-mass spectrometry ((ICP-MS)) was used to determine three toxic (Ni, As, Cd) and six essential trace elements (Cr, Mn, Co, Cu, Zn, Se) in blood serum of patients with hypothyroidism (Hy group) and healthy people (control group), in order to set the experimental conditions for accurate determination of a unique profile of these elements in hypothyroidism. Method validation was performed with standard reference material of the serum by varying the sample treatment with both standard and collision mode for analysis of elements isotopes. Quadratic curvilinear functions with good performances of models and the lowest detection limits were obtained for 52 Cr, 66 Zn, 75 As, 112 Cd in collision mode, and 55 Mn, 59 Co, 60 Ni, 65 Cu, 78 Se in standard mode. Treatment of serum samples with aqueous solution containing nitric acid, Triton X-100 and n-butanol gave the best results. Chemometric tools were applied for discrimination of patients with hypothyroidism. All nine elements discriminated Hy group of samples with almost the same discriminating power as indicated by their higher values for this group of patients. Statistically significant correlation (p hypothyroid state. Copyright © 2018 Elsevier GmbH. All rights reserved.

  1. PIXE analysis of trace elements in cetacean teeth

    International Nuclear Information System (INIS)

    Mitani, Yoko; Arai, Nobuaki; Sakamoto, Wataru; Yoshida, Koji

    1997-01-01

    PIXE was adopted for analysis of trace elements in teeth of two species of cetaceans, sperm whale (Physeter microcephalus) and pantropical spotted dolphin (Stenella attenuata). The analyses were performed along with the growth layer of the teeth, which is formed annually, suitable for age determination. Mn, Fe, Cu, Zu and Sr were detected in the teeth of sperm whale and pantropical spotted dolphin. Among these trace elements, gradual increase was observed for Zn/Ca ratio in the sperm whale's teeth. (author)

  2. Trace elements in relation to cardiovascular diseases

    Energy Technology Data Exchange (ETDEWEB)

    Masironi, R [World Health Organization, Cardiovascular Diseases Unit, Geneva (Switzerland); Parr, R M [International Atomic Energy Agency, Medical Applications Section, Vienna (Austria)

    1973-07-01

    For the past four years the World Health Organization and the International Atomic Energy-Agency have been jointly coordinating investigations at an international level on the role possibly played by stable trace elements in the aetiology of cardiovascular diseases, and the use of nuclear techniques in studying these elements. (author)

  3. Trace element analysis in soy sauce. 2

    International Nuclear Information System (INIS)

    Haruyama, Yoichi; Saito, Manabu; Tomita, Michio; Yoshida, Koji.

    1994-01-01

    Trace elements in four kinds of soybean and three kinds of salt have been measured by means of in-air PIXE. In soybeans, which were made in Japan, America, Canada and China, six kinds of trace elements were detected, such as Mn, Fe, Ni, Cu, Zn and Br. The concentration of these elements varied depending on the place they were made. American soybean showed characteristic feature compared with other soybeans. As to the bromine concentration, American soybean contains ten times as much as Japanese one. In salts Br and Sr were detected. (author)

  4. The use of cation exchange matrix separation coupled with ICP-MS to directly determine platinum group element (PGE) and other trace element emissions from passenger cars equipped with diesel particulate filters (DPF)

    Energy Technology Data Exchange (ETDEWEB)

    Cairns, Warren R.L.; Cozzi, Giulio [Institute for the Dynamics of Environmental Processes-CNR, Venice (Italy); De Boni, Antonella; Gabrieli, Jacopo [University of Venice, Department of Environmental Science, Venice (Italy); Asti, Massimo; Merlone Borla, Edoardo; Parussa, Flavio [Centro Ricerche Fiat, Orbassano (Italy); Moretto, Ezio [FIAT Powertrain Technologies S.p.A, Turin (Italy); Cescon, Paolo; Barbante, Carlo [University of Venice, Department of Environmental Science, Venice (Italy); Institute for the Dynamics of Environmental Processes-CNR, Venice (Italy); Boutron, Claude [Laboratoire de Glaciologie et Geophysique de l' Environnement, UMR CNRS 5183, B.P. 96, Saint Martin d' Heres Cedex (France)

    2011-03-15

    Inductively coupled plasma-mass spectrometry coupled with cation exchange matrix separation has been optimised for the direct determination of platinum group element (PGE) and trace element emissions from a diesel engine car. After matrix separation method detection limits of 1.6 ng g{sup -1} for Pd, 0.4 ng g{sup -1} for Rh and 4.3 ng g{sup -1} for Pt were achieved, the method was validated against the certified reference material BCR 723, urban road dust. The test vehicle was fitted with new and aged catalytic converters with and without diesel particulate filters (DPF). Samples were collected after three consecutive New European Driving Cycle (NEDC) of the particulate and ''soluble'' phases using a home-made sampler optimised for trace element analysis. Emission factors for the PGEs ranged from 0.021 ng km{sup -1} for Rh to 70.5 ng km{sup -1} for Pt; when a DPF was fitted, the emission factors for the PGEs actually used in the catalysts dropped by up to 97% (for Pt). Trace element emission factors were found to drop by a maximum of 92% for Ni to a minimum of 18% for Y when a DPF was fitted; a new DPF was also found to cause a reduction of up to 86% in the emission of particulate matter. (orig.)

  5. Determination of elemental concentrations at trace levels in alumina by charged particle activation analysis using proton beam from VEC accelerator

    International Nuclear Information System (INIS)

    Datta, J.; Dasgupta, S.; Chowdhury, D.P.; Verma, R.

    2015-01-01

    The elemental impurities have been determined in high purity alumina material used in nuclear reactors at ppb (μg kg -1 ) to ppm (mg kg -1 ) levels by CPAA using proton beam from VEC machine. Proton beam has the advantage of high cross section for (p, n) reaction to produce suitable nuclide for activation analysis by instrumental approach. The cross sections of higher reaction channels like (p, 2n), (p, pn) are found to be less than 1 mb below 13 MeV proton by theoretical calculation using ALICE 91 computer code. Therefore, 13 MeV proton beam was used to irradiate the alumina samples along with standards, Lake (IAEA-SL -1 ) and Marine (PACS-2) sediments, both in pellet and powder forms. The irradiation was carried out with 50 nA to 1μA beam current for 10 min to 10 h depending on types of samples and standards. The beam current was measured by Faraday cup and also checked by putting Ti monitoring foil before the target. Ni is determined by (p, pn) reaction using 18 MeV proton as there is no suitable product from (p, n) reaction. The counting measurements of irradiated samples were performed with a high resolution γ-spectrometer using HPGe detector (relative efficiency - 40%, resolution - 2.0 keV at 1332 keV) coupled to a PC based 8 k MCA. The validation of the CPAA results has been carried out by INAA with the same alumina samples, carried out in Dhruva reactor with neutron flux 10 14 cm 2 s -1 using standards IAEA-SL-1 and PACS-2

  6. The use of x-ray fluorescence technique (XRF) in the determination of trace elements in environmental study: a case study for sediments and soils

    International Nuclear Information System (INIS)

    Hamzah Mohamad

    1997-01-01

    A specific X-ray fluorescence technique (XRF) was developed to determine the concentrations of nine common and significant trace elements in sediments and soils, i.e. two of the common materials used in environmental studies. The elements are Ba, Cr, Cu, Fe, Mn, Ni, Pb, V and Zn. A total of 22 international reference materials of rocks, soils, minerals, ores and sediments were employed to construct nine calibration curves, all of which depict linear correlation of concentration-intensity, with correlation coefficients of 0.9 or better. The accuracy of determination is implied from the relative differences between the observed and suggested values in four reference materials: USGS SCO-1, shale; CCRMP SO-1, soil; CCRMP CO-2, soil; and SARM 42, soil. The determinations of four elements are considered as accurate, with relative errors of smaller than 10%; they are Fe (5%), Mn (6%), Cr (8%), and Cu (9%). Only a moderate accuracy has been achieved in the determinations of Ba (13%), Zn (18%) and V (21 %). Ni and Ph results are associated with larger errors. The developed technique is considered rapid, whereby nine elements in 30 samples in the form of pressed powder briquettes can be analysed in 8 hours. Without extrapolating the calibration curves, the method is suitable to analyse elements in soils and sediments in the following ranges of concentrations: Ba, 0-1500 ppm; Cr, 0-3000 ppm; Cu, 0-300 ppm; Fe, 0.7%; Mn, 0-1000 ppm; Ni, 0-300 ppm; Pb, 0-70 ppm; V, 0-300 ppm and Zn, 0-270 ppm

  7. Comparison of the effectiveness of various procedures for the rejection of outlying results and assigning consensus values in interlaboratory programs involving determination of trace elements or radionuclides

    International Nuclear Information System (INIS)

    Dybczynski, R.

    1980-01-01

    Rejection of outlying results is usually necessary in the evaluation of interlaboratory comparisons, especially those involving trace elements and low-level activity measurements. The performance of several criteria (Dixon's test, Grubbs' test, coefficient of skewness test, and coefficient of kurtosis test) is described; authentic data sets from intercomparison runs on trace element or radionuclide determinations in spiked samples are used. The existence of 'masking effects' in certain cases is demonstrated. It is shown that concurrent use of all four criteria at small (0.01) or moderate (0.05) significance levels gives better results than the use of any single test. The use of all four criteria at α = 0.05 followed by calculation of overall mean and pertinent confidence limits is suggested as a general method of data handling in interlaboratory comparison. This method normally ensures good selectivity of outlier rejection while avoiding excessive rejections, and results in generally good agreement between the 'true' value and the final overall mean. The use of this approach for the establishment of recommended values in candidate reference materials is demonstrated and its advantages and limitations are discussed. The results are further compared with those obtained by other methods of data evaluation (Student's test, dominant cluster mode and gamma transformation). (Auth.)

  8. Multianalytical determination of trace elements in atmospheric biomonitors by k0-INAA, ICP-MS and AAS

    Science.gov (United States)

    Freitas, M. C.; Pacheco, A. M. G.; Dionísio, I.; Sarmento, S.; Baptista, M. S.; Vasconcelos, M. T. S. D.; Cabral, J. P.

    2006-08-01

    Elemental contents of atmospheric biomonitors—epiphytic lichens and tree bark, exposed in continuous and discontinuous modes—have been assessed through k0-standardised instrumental neutron activation analysis ( k0-INAA) (two different institutions), inductively coupled plasma mass spectrometry (ICP-MS) and atomic absorption spectrometry (AAS). Certified reference materials—ISE-921 (river clay), NIST-1547 (peach leaves), ICHTJ-INCT-TL-1 (tea leaves; TL-1 hereinafter) and IAEA-336 (lichen material), and nonparametric statistics—rank-order correlations (Spearman RS) and enhanced-sign tests (Wilcoxon T)—were used for analytical control and data comparison, respectively. In general, quality of procedures was deemed good, except for k0-INAA in determining Br, Cu and Na, all likely affected by high counting statistics, and/or contamination issues (the latter). Results for Cu, Ni, Pb and Sr (by both ICP-MS and AAS) revealed that, despite an outstanding correlation (asymptotic p=0.000), they could be viewed as statistically equal for Cu only: AAS tended to yield higher values for Pb and Ni, and lower ones for Sr. The comparison between ICP-MS and k0-INAA data from TUDelft, for Al, Ca, Cu, Mg, Mn, Na, Ti and V, showed an excellent correlation (as above) and random (relative) magnitude for Cu, Mg, Mn and Ti only: ICP-MS tended to yield higher values for Al, Na and V, and lower ones for Ca, whereas between k0-INAA data from TUDelft and ITN, for Br, Ca and Na, resulted in systematically higher [Br] and [Ca] variates from TUDelft, even if all corresponding data sets were found to correlate at stringent significance levels. In a few cases, though—Ca, Sr in lichens; Pb in bark—matrix effects did appear to interfere in the outcome of matched-pairs, signed-rank tests, since random hierarchy of variates could be asserted just when lichen and bark data sets were processed separately.

  9. Preconcentration of trace elements by using 1-(2-Pyridylazo-2-naphthol functionalized Amberlite XAD-1180 resin and their determination by FAAS

    Directory of Open Access Journals (Sweden)

    Tokalioglu Serife

    2006-01-01

    Full Text Available In this study, Amberlite XAD-1180 resin functionalized by 1-(2-pyridylazo-2-naphthol (PAN was synthesized and the resulting resin was used for preconcentration of Cr(III, Mn(II, Fe(III, Ni(II, Cu(II, Cd(II and Pb(II elements present at trace levels in different matrices. For this purpose, the copolymer was nitrated, reduced to the corresponding amine, converted to the diazonium salt with nitrite and reacted with PAN to produce the XAD-1180-PAN chelating resin. For the described method, the effect of some analytical parameters, such as pH, sample volume, resin amount, flow rates of uptake and stripping, volume and type of eluent, on the recovery of the trace elements was investigated. The metals retained on the XAD-1180-PAN resin were eluted by 2 mol L-1 HNO3. The influence of matrix ions, i.e., Na(I, K(I, Ca(II and Mg(II, on the recovery of trace elements was also examined by using the developed method when they occurred both individually and together. The repeatability of the method at the optimum conditions determined experimentally was investigated. The recovery values for all the elements, except for Cr(III, were found to be >92% and the relative standard deviation was <8.5%. The 3s/b detection limits for Cr(III, Mn(II, Fe(III, Ni(II, Cu(II, Cd(II and Pb(II were found to be 4.1, 0.13, 2.7, 1.2, 0.19, 0.06 and 0.13 µg L-1, respectively. The developed method was utilized for preconcentration and determination of Mn(II, Fe(III, Ni(II, Cu(II, Cd(II and Pb(II in tap water, rain water, and stream water, and of Ni(II, Cd(II and Pb(II in a certified reference material (RM 8704 Buffalo river sediment by flame atomic absorption spectrometry (FAAS.

  10. Nutritional values of trace elements in dried desserts

    International Nuclear Information System (INIS)

    Kyritsis, A.; Kanias, G.D.; Tzia, C.

    1997-01-01

    Desserts are the most aromatic and delicious parts of meals, and also a source of nutrient trace elements for the human body. In this work, instrumental neutron activation analysis has been applied to determine the trace elements antimony, chromium, cobalt, iron, manganese, potassium, rubidium, scandium, sodium and zinc in creme caramel, ice-creams, jellies and mousse dried desserts from the Greek market. According to our results, their classification as nutrient trace element sources for the human body is: mousse>ice-cream> creme caramel> jelly. Among the different studied flavours, chocolate and its derivatives are the richest in nutrient trace elements. Moreover, the consumption of one portion of a chocolate mousse dessert can offer to the human body about 60% of the daily required chromium, 40% of the daily required iron, 10% of the daily required manganese and potassium and 4% of the daily required sodium. (author)

  11. Influence of trace elements on fluoride uptake by teeth

    Energy Technology Data Exchange (ETDEWEB)

    Chaudhri, M A [Austin Hospital, Heidelberg (Australia). Dept. of Medical Physics; Melbourne Univ., Austin (Australia). Dept. of Medicine); Crawford, A [Melbourne Univ., Parkville (Australia). School of Physics

    1981-03-01

    To investigate the effect of various trace elements on fluoride uptake by teeth, the concentrations of F and other trace elements have been simultaneously determined in different regions of the teeth from children of South Australia. Teeth cross sectioned along the median plane have been used in these investigations, and their inside enamel, dentine and amelodentinal junctions investigated separately for the trace elemental composition. Fluoride has been determined by observing the 6-7 MeV gammas for the /sup 19/F(p,..cap alpha gamma..)/sup 16/O reaction, C by activation through the /sup 12/C(/sup 3/He,n)/sup 14/O reaction, while other trace elements have been measured by the thick target PIXE technique. Linear correlation coefficients have been calculated between the F concentrations in teeth and those of other trace elements observed. Fluoride is found to correlate best with C, Cu and Pb, poorly with Fe, Sr, Ni and Ag, while with Br and Zn it has-ve coefficients. Student's t-test has been applied to the data to examine the significance of the variation of Fand other trace elements amongst different dental tissues from healthy and diseased teeth.

  12. Trace elements levels in centenarian 'dodgers'.

    Science.gov (United States)

    Alis, Rafael; Santos-Lozano, Alejandro; Sanchis-Gomar, Fabian; Pareja-Galeano, Helios; Fiuza-Luces, Carmen; Garatachea, Nuria; Lucia, Alejandro; Emanuele, Enzo

    2016-05-01

    Trace element bioavailability can play a role in several metabolic and physiological pathways known to be altered during the aging process. We aimed to explore the association of trace elements with increased lifespan by analyzing the circulating levels of seven trace elements (Cr, Cu, Fe, Mn, Mo, Se and Zn) in a cohort of healthy centenarians or 'dodgers' (≥100 years, free of major age-related diseases) in comparison with sex-matched younger elderly controls. Centenarians showed significant lower Cu (783.7 (76.7, 1608.9) vs 962.5 (676.3, 2064.4)μg/mL, Pdodgers', and, therefore, at least partly, be involved in the healthy aging phenotype shown by these subjects. These results should be confirmed in larger cohorts of other geographic/ethnic origin and the potential cause-effect association tested in mechanistic experimental settings. Copyright © 2016 Elsevier GmbH. All rights reserved.

  13. A study on human hair element content as monitor for trace elements pollution in Eg

    International Nuclear Information System (INIS)

    Tadros, N.; Metwally, E.

    2004-01-01

    Trace element content in human is a suitable indicator of exposure to trace element pollutants. Concentration levels of 12 trace elements in human head hair samples collected from more than 23 individuals have been determined. The collected hair samples were classified into four groups collected from workers at nuclear research center and others far away from the center. Neutron activation analysis technique was used in the preset study. The data reported for trace elements content in different hair samples were discussed. Significant differences were observed for several elements levels. comparative studies demonstrated that the concentration of some elements in hair of exposed workers, are greater than those corresponding to non exposed workers. Also, there was no clear significant correlation between the elements content of different hair samples and the age of the donors

  14. Trace Element Analysis of Selenium

    International Nuclear Information System (INIS)

    Soliman, M.S.A.

    2010-01-01

    The present thesis divided into four chapters as follows:Chapter (1):This chapter contains an introduction on different oxidation states of organic and inorganic species for selenium in environmental and biological samples, the process for separation of selenium from these samples and the importance of selenium as a component for these samples. Also gives notes about the techniques which are used in the elemental analysis for selenium species and the detection limits for selenium in these techniques, selenium species in human body and the importance of these species in protecting the body from the different types of cancer and the sources of selenium in environmental samples (soil and water) and distribution levels of selenium in these samples.Chapter (2):This chapter is divided into two parts :The first part deals with the sample collection process for environmental samples (underground water, soil) and the wet digestion ( microwave digestion ) process of soil samples. It also contains the theory of work of the closed microwave digestion system.The second part contains detailed information concerning the theoretical considerations of the used analytical techniques. These techniques include Hydride generation - Atomic Absorption Spectrometer (HG-AAS), Inductively Coupled Plasma Mass Spectrometer (ICP-MS) and Neutron Activation Analysis (NAA).Chapter (3): This chapter includes the methods of sampling, sample preparation, and sample digesition. The measures of quality assurance are disscused in this chapter. It describes in details the closed microwave digestion technique and the analytical methods used in this study which are present in Central Laboratory for Elemental and Isotopic Analysis (CLEIA) and the Egypt Second Research Reactor (ETRR-2). The described techniques are Atomic Absorption Spectrometer (AAS 6 vario, Analytical Jena GmbH, Germany), JMS-PLASMAX2 Mass Spectrometer (ICP-MS) and the Egypt Second Research Reactor (NAA).

  15. Application of neutron activation analysis to the determination of minor-and trace elements in magnesite ore

    International Nuclear Information System (INIS)

    Sepulveda Munita, C.J.A.; Atalla, L.T.

    1979-01-01

    A method employing analysis with thermal neutrons was developed for analyzing magnesite samples coming from the States do Ceara and Bahia (Brazil). Ten samples were analyzed. Qualitative analysis of the samples indicated the presence of Mn, Fe, Sc, Ca, Cu, Co and some of the lanthanides. Mn was analyzed by non-destructive activation analysis and the other elements were analyzed, individually or in group, after sample dissolution with 8 N HCl solution. A detailed study of the possible interferences in neutron activation analysis of the elements considered was also undertaken. The precision and accuracy of the results obtained and the sensitivity of the method are discussed. (Author) [pt

  16. The laser microprobe mass analyser for determining partitioning of minor and trace elements among intimately associated macerals: an example from the Swallow Wood coal bed, Yorkshire, UK

    Science.gov (United States)

    Lyons, P.C.; Morelli, J.J.; Hercules, D.M.; Lineman, D.; Thompson-Rizer, C. L.; Dulong, F.T.

    1990-01-01

    A study of the elemental composition of intimately associated coal macerals in the English Swallow Wood coal bed was conducted using a laser microprobe mass analyser, and indicated a similar trace and minor elemental chemistry in the vitrinite and cutinite and a different elemental signature in the fusinite. Three to six sites were analysed within each maceral during the study by laser micro mass spectrometry (LAMMS). Al, Ba, Ca, Cl, Cr, Dy, F, Fe, Ga, K, Li, Mg, Na, S, Si, Sr, Ti, V, and Y were detected by LAMMS in all three macerals but not necessarily at each site analysed. The signal intensities of major isotopic peaks were normalized to the signal intensity of the m z 85 peak (C7H) to determine the relative minor- and trace-element concentrations among the three dominant macerals. The vitrinite and the cutinite were depleted in Ba, Ca, Dy, Li, Mg, Sr, and Y relative to their concentrations observed in the fusinite. The cutinite was distinguished over vitrinite by less Ti, V, Cr and Ca, and K Ca $ ??1 (relative signal intensities). The fusinite, relative to the cutinite and vitrinite, was relatively depleted in Cr, Sc, Ti, and V. The fusinite, as compared with both the cutinite and vitrinite, was relatively enriched in Ba, Ca, Dy, Li, Mg, Sr, and Y, and also showed the most intense m z 64, 65, 66 signals (possibly S2+, HS2+, H2S2+, respectively). The LAMMS data indicate a common source for most elements and selective loss from the maceral precursors in the peat or entrapment of certain elements as mineral matter, most likely during the peat stage or during early diagenesis. The relatively high amounts of Ba, Ca, Dy, Li, Mg, Sr, and Y in the fusinite are consistent with micron and submicron mineral-matter inclusions such as carbonates and Ca-Al phosphates (probably crandallite group minerals). Mineralogical data on the whole coal, the LAMMS chemistry of the vitrinite and cutinite, and scanning electron microscopy/energy dispersive X-ray analysis (SEM/EDAX) of

  17. Report on the quality control study NAT-6 for the determination of trace and minor elements in two moss samples

    International Nuclear Information System (INIS)

    Beise, A.; Smodis, A.

    2001-12-01

    A quality control study was organized on two moss materials. The materials were Pleuroziurn Schreberi species, a carpet forming moss which can be found throughout northern Europe. One material was collected from an unpolluted area and the other from a mining area in Scandinavia. 17 laboratories from 16 countries participated in the study, providing 26 sets of results. The following analytical methods were used: neutron activation analysis (NAA), inductive coupled plasma atomic emission spectrometry (ICP - AES), inductively coupled plasma mass spectrometry (ICP-MS), isotope-dilution thermal ionisation mass spectrometry IDTIMS) atomic absorption spectrometry (AAS), atomic fluorescence spectrometry (AFS) voltainetry V) and X-ray fluorescence spectrometry XRF). The results were evaluated following the standard IAEA procedures for (1) an interlaboratory comparison exercise and (2) a proficiency test using target values from the literature. For the moss sample M-1, 409 laboratory mean values for 47 elements were reported. More than 4 mean values were obtained for 28 measurands and these were statistically evaluated. Only 7 % 27 values) of the results were detected as outliers by the statistical data evaluation. There was good agreement for the results obtained by different methods for 21 elements (Al, Ba, Ca, Cd, Co, Cs, Cu, Fe, K, La, Mg, Mn, Na, Ni, Pb, Rb, Sb, Sc, Se, V, and Zn). Results for Br, Ce, Sn and Th were obtained only by NAA. Statistical evaluation of the data revealed satisfactory values for As, Hg and Cr. The results and statistical parameters are listed in the appendices I and II. The results were also evaluated as a proficiency test using target values from the literature. Precision and accuracy criteria were applied to 15 elements. 234 laboratory mean values were reported for these elements, 47 values (20%) did not pass the set proficiency test criteria. The individual laboratory results are listed in appendix IV. For the moss sample M-2, 347 laboratory

  18. Determination of essential trace elements in wine by neutron activation analysis; Determinacao de elementos essenciais em vinhos por analise por ativacao com neutrons

    Energy Technology Data Exchange (ETDEWEB)

    Daniele, Anna Paula

    2016-07-01

    Several studies have been carried out for determining essential elements in foodstuffs, including wine, due to its important nutritional role in human body functions. It was shown that daily consumption of wine in moderation contributes significantly to the needs of essential elements in human body such as Ca, Co, Cr, Fe, K, Mg, Mn, Zn, V, among others, and has health benefits in the prevention of numerous diseases and longer life expectancy, related in particular to the intake of antioxidants such as polyphenolic compounds. Trace elements are good indicators of origin of wines and their concentrations can be used as criteria to ensure authenticity, quality and show that the tolerance limits established by law were respected throughout the production process. However, although Brazilian wine industry is among the 15 largest in the world, analytical studies for organic and inorganic compounds of wine content are still small when compared to other major producers. In this sense, this study aimed to evaluate some procedures of wine sample preparation to determine essential elements by Instrumental Neutron Activation Analysis (INAA) and compare the results with those determined by Inductively Coupled Plasma Atomic Emission Spectrometry (ICP OES). Three sample preparation procedures were studied: freeze-drying, evaporation and dry ashing. The parameters studied were precision, accuracy and detection limit. ANOVA and Tukey-Kramer tests were applied to verify the statistical differences between the mean values obtained by the three wine preparation procedures for INAA with those means obtained by ICP OES. It was noticed that about 60% of results obtained by freeze-drying agreed with those obtained by ICP OES. (author)

  19. Trace elements in glucometabolic disorders: an update

    Directory of Open Access Journals (Sweden)

    Wiernsperger Nicolas

    2010-12-01

    Full Text Available Abstract Many trace elements, among which metals, are indispensable for proper functioning of a myriad of biochemical reactions, more particularly as enzyme cofactors. This is particularly true for the vast set of processes involved in regulation of glucose homeostasis, being it in glucose metabolism itself or in hormonal control, especially insulin. The role and importance of trace elements such as chromium, zinc, selenium, lithium and vanadium are much less evident and subjected to chronic debate. This review updates our actual knowledge concerning these five trace elements. A careful survey of the literature shows that while theoretical postulates from some key roles of these elements had led to real hopes for therapy of insulin resistance and diabetes, the limited experience based on available data indicates that beneficial effects and use of most of them are subjected to caution, given the narrow window between safe and unsafe doses. Clear therapeutic benefit in these pathologies is presently doubtful but some data indicate that these metals may have a clinical interest in patients presenting deficiencies in individual metal levels. The same holds true for an association of some trace elements such as chromium or zinc with oral antidiabetics. However, this area is essentially unexplored in adequate clinical trials, which are worth being performed.

  20. Determination of trace element concentrations and stable lead, uranium and thorium isotope ratios by quadrupole-ICP-MS in NORM and NORM-polluted sample leachates

    International Nuclear Information System (INIS)

    Mas, J.L.; Villa, M.; Hurtado, S.; García-Tenorio, R.

    2012-01-01

    Highlights: ► Polluted sediment and NORM samples. ► An efficient yet fast process allowing multi-parametric determinations in 206 Pb/ 207 Pb/ 208 Pb, 238 U/ 234 U and 232 Th/ 230 Th isotope ratios using a single sample aliquot and a single instrument (ICP-QMS). Eichrom UTEVA ® extraction chromatography minicolumns were used to separate uranium and thorium in sample leachates. Independent ICP-MS determinations of uranium and thorium isotope ratios were carried out afterwards. Previously a small aliquot of the leachate was used for the determination of trace element concentrations and lead isotope ratios. Several radiochemical arrangements were tested to get maximum performances and simplicity of the method. The performances of the method were studied in terms of chemical yields of uranium and thorium and removal of the potentially interfering elements. The established method was applied to samples from a chemical industry and sediments collected in a NORM-polluted scenario. The results obtained from our method allowed us to infer not only the extent, but also the sources of the contamination in the area.

  1. Report on the intercomparison run NAT-5 for the determination of trace and minor elements in two lichen samples

    International Nuclear Information System (INIS)

    Bleise, A.; Smodis, B.

    1999-12-01

    An intercomparison exercise was organized for two lichen materials, one from an unpolluted area in Portugal, the other from a mining area in Austria. 15 laboratories from 15 countries participated in the analysis providing 17 sets of results and using the following analytical methods: neutron activation analysis (NAA), inductive coupled plasma atomic emission spectrometry (ICP-AES), inductively coupled plasma mass spectrometry (ICP-MS), atomic absorption spectrometry (AAS) and particle induced X-ray emission analysis (PIXE). In all results were obtained for 51 elements for the sample lichen L-1, and for 47 elements for the sample lichen L-2. For the sample lichen L-1, more than 4 individual laboratory mean values were reported for 28 elements. Out of these, there was good agreement for the results obtained by different methods for 17 elements (Ba, Br, Ca, Cd, Cl, Co, Cu, Hg, K, La, Mn, Na, Pb, Rb, Sc, V, and Zn). Results for As, Ce, Cs, Sb and Se were available only by NAA. Statistical evaluation of the data revealed satisfactory values for Fe, Mg and Cr. In other cases the wide range of results did not permit a thorough evaluation. The final results for Al, Ni and Ti were unsatisfactory due to excessive dispersion observed in the reported ranges. For Ag, Au, Bi, Dy, Eu, Ga, Hf, I, Lu, Mo, Nd, P, S, Si, Sm, Sr, Ta, Tb, u, W, Yb and Zr only a few mean values were reported, and statistical evaluation was not possible. These results are simply listed in the Appendices I and II without any statistical data. For the sample lichen L-2, which was actually the IAEA reference material IAEA-336, 15 elements out of the 26 evaluated showed good agreement between different methods (Br, Ca, CI, Co, Cu, Fe, Hg, La, Mn, Na, Ni, Pb, Rb, V and Zn). For As, Ce, Cs, Sb, Sc and Se only NAA was used. Acceptable values were revealed for K, Mg and Cr. The results obtained for Al and Ti were unsatisfactory because the values showed excessive dispersion. Less than 5 laboratory means were

  2. High accuracy determination of trace elements in NIST standard reference materials by isotope dilution ICP-MS

    International Nuclear Information System (INIS)

    Paulsen, P.J.; Beary, E.S.

    1996-01-01

    At NIST (National Institute of Standards and Technology), ICP-MS ID (inductively coupled mass spectrometry isotope dilution) has been used to certify a wide range of elements in a variety of materials with high accuracy. Both the chemical preparation and instrumental procedures are simpler than with other ID mass spectrometric techniques. The ICP-MS has picogram/ml detection limits for most elements using fixed operating parameters. Chemical separations are required only to remove an interference (from molecular ions as well as isobaric atoms), or to pre-concentrate the analyte. For example, chemical separations were required for the analysis of SRM 2711, Montana II Soil, but not for boron in peach leaves, SRM 1547.(3 refs., 3 tabs., 2 figs

  3. Determination of natural radionuclides from 238U and 232Th series, trace and major elements in sediment cores from baixada Santista and evaluation of impacted areas

    International Nuclear Information System (INIS)

    Damatto, Sandra Regina

    2010-01-01

    Baixada Santista is the region of higher population of the coast of Sao Paulo State, where it is located the largest port in Latin America, in the city of Santos, and the most important industrial complex of Latin America, in the city of Cubatao. This region has received in recent years a considerable load of industrial and domestic effluents in its water bodies, as a direct result of the industrial and port activities and the large population growth in recent decades, and is considered nowadays highly impacted. In the present study sediment cores were collected in the estuary of Santos-Cubatao, in the estuary of Sao Vicente, in the channel of Bertioga and Santos Bay, in order to determine the concentration of trace and major elements and natural radionuclides from the 238 U and 232 Th series. The techniques used were neutron activation analysis, X-ray fluorescence and gamma spectrometry, respectively. The obtained values for the elements Cr, Sb, Ta and Zn in some cores, are higher than data from literature, and can indicate a possible anthropic contribution. Comparing the obtained values of Cr and Zn elements determined in the sediment cores with the values of TEL and PEL index for sediment quality, it was verified that the studied region presents Cr levels higher than TEL in Santos-Cubatao estuary and Bertioga channel and Zn element presented values higher than TEL for some core slices of Santos-Cubatao estuary, for one core of Sao Vicente estuary, one core in Bertioga channel and Santos Bay. For the other elements, the values obtained in this study can be considered as reference values for the region. Although the element As presented higher values than the TEL in all the studied environments, the concentrations obtained are of the same order of magnitude as literature data and, therefore, can be considered also as reference values for the region. No enrichment was found for the major elements in all the ecosystems studied, with the exception for the element P

  4. Survey of currently available reference materials for use in connection with the determination of trace elements in biological and environmental materials

    International Nuclear Information System (INIS)

    Muramatsu, Y.; Parr, R.M.

    1985-12-01

    This report focuses on analytical reference materials which have been developed for use in connection with the determination of toxic and essential trace elements in biomedical and health-related environmental samples. Data are reported on 60 biological and 40 environmental (non-biological) reference materials from 11 suppliers. Certified concentration values (or their equivalents) and non-certified concentration values (or information values) are presented in various tables which are intended to help the user select a reference material that matches as closely as possible (i.e. with respect to matrix type and concentration of the element of interest) the ''real'' samples that are to be analysed. These tables have been generated from a database characterized by the following parameters: total number of reference materials=100; total number of elements recorded=69; total number of concentration values recorded=1771. Also included in the report is information (where available) on the cost of each material, the unit weight or volume supplied, and the minimum weight of material recommended for analysis. (author)

  5. Study on trace element determination in liver samples of great-white-egret Ardea alba Linnaeus, 1758 (Ardeidae, Aves) for environmental contamination biomionitoring

    International Nuclear Information System (INIS)

    Silva, Rita de Cassia A.; Saiki, Mitiko

    2009-01-01

    Predatory birds such as herons have been used as bioindicators of pollution since they are at the top of their food webs. The tissues of these animals are analyzed for assessing environmental pollution caused by toxic elements. In the present study, adequate experimental conditions were established for determination of trace elements concentrations in the liver samples of Great-white-egret (Ardea alba Linnaeus, 1758) for further application of this specimens as a bioindicator of environmental contamination. Four liver samples were collected from Greatwhite- egrets found in the metropolitan region of Sao Paulo and were they analyzed by the method of neutron activation analysis (NAA). Concentrations of the elements Br, Co, Cs, Fe, Na, Rb, Se and Zn were measured in these liver tissues. The findings of this present study demonstrated that the established procedure for liver sample treatment was appropriate to obtain a homogeneous sample. The method of neutron activation analysis (NAA) was very promising for liver sample analysis for evaluation of environmental contamination. (author)

  6. Study on trace element determination in liver samples of great-white-egret Ardea alba Linnaeus, 1758 (Ardeidae, Aves) for environmental contamination biomionitoring

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Rita de Cassia A.; Saiki, Mitiko, E-mail: rcsilva@ipen.b, E-mail: mitiko@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2009-07-01

    Predatory birds such as herons have been used as bioindicators of pollution since they are at the top of their food webs. The tissues of these animals are analyzed for assessing environmental pollution caused by toxic elements. In the present study, adequate experimental conditions were established for determination of trace elements concentrations in the liver samples of Great-white-egret (Ardea alba Linnaeus, 1758) for further application of this specimens as a bioindicator of environmental contamination. Four liver samples were collected from Greatwhite- egrets found in the metropolitan region of Sao Paulo and were they analyzed by the method of neutron activation analysis (NAA). Concentrations of the elements Br, Co, Cs, Fe, Na, Rb, Se and Zn were measured in these liver tissues. The findings of this present study demonstrated that the established procedure for liver sample treatment was appropriate to obtain a homogeneous sample. The method of neutron activation analysis (NAA) was very promising for liver sample analysis for evaluation of environmental contamination. (author)

  7. 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. Copyright © 2010 Elsevier B.V. All rights reserved.

  8. Macro-Elements and Trace Elements in Cereal Grains Cultivated in Latvia

    Directory of Open Access Journals (Sweden)

    Jākobsone Ida

    2015-09-01

    Full Text Available Cereal-based foods have great importance in the compensation of micro- and trace element deficiency, because 50% of the foods produced worldwide are made up of cereal grains. The aim of the research was to determine the concentration of macro-elements and trace elements in different cereals cultivated in Latvia. Various cereals were used in the research: rye (n = 45, barley (n = 54, spring wheat (n = 27, winter wheat (n = 53, triticale (n = 45 and oats (n = 42. Thirteen macro- and trace elements (Cd, Pb, Ni, Cr, Al, Cu, K, Na, Mn, Fe, Zn, Mg, Ca were determined in cereal grain samples (n = 266. Macro-elements and trace elements varied significantly (p < 0.01 or p < 0.001. The highest concentrations of macro- and trace elements were found in oats and the lowest in rye. The obtained data will expand the opportunity for food and nutrition scientists to evaluate content of the examined elements in grain products, and dietary consumption (bioavailability of the examined macro-elements and trace elements.

  9. Analysis of trace elements in opal using PIXE

    Energy Technology Data Exchange (ETDEWEB)

    Hinrichs, Ruth, E-mail: ruth.hinrichs@ufrgs.br [Instituto de Geociências, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS (Brazil); Programa de Pós-graduação em Física, UFRGS, Porto Alegre, RS (Brazil); Bertol, A.P.L. [Programa de Pós-graduação em Física, UFRGS, Porto Alegre, RS (Brazil); Vasconcellos, M.A.Z. [Programa de Pós-graduação em Física, UFRGS, Porto Alegre, RS (Brazil); Instituto de Física, UFRGS, Porto Alegre, RS (Brazil)

    2015-11-15

    Particle induced X-ray emission (PIXE) analysis is particularly important for the analysis of trace elements of precious samples, being one of the few methods to determine elements with ppm concentration that does not affect sample integrity. A PIXE methodology for trace element analysis in opal was developed. To avoid detector count saturation due to the high number of Si-Kα X-rays generated in the sample, several filters were employed to optimize the reduction of the Si-Kα signal, while maintaining acceptable intensities of the other relevant X-ray lines. Two proton beam energies were tested, to establish the signal to noise ratio in different X-ray energies. Spectra were fitted with the software GUPIX, using a matrix composition determined with electron beam excited energy dispersive X-ray spectrometry. Above the energy of the silicon X-ray, several trace elements were quantified.

  10. Trace element deficiency and its diagnosis by radioisotope injection

    International Nuclear Information System (INIS)

    Kirchgessner, M.; Schwarz, F.J.

    1976-01-01

    The metabolism of trace elements is subject to certain mechanisms of homeostatic regulation. The supply status of the trace elements, iron, copper, zinc and manganese has definite effects on their respective extent of intestinal absorption, retention and intestinal excretion. Experimental studies show that there is an increase in intestinal absorption and retention, and a decrease in turnover rate and endogenous excretion of these trace elements in response to deficient dietary intake. On the basis of these results, three models are discussed for the use of radioisotopes in the diagnosis of situations of trace element deficiency: (1) Determination of the intestinal absorption of an orally administered radioisotope dose by measuring the activity of blood; (2) Determination of the retention of a parenterally administered dose in blood or plasma; and (3) Determination of the endogenous faecal excretion of a parenterally administered dose. The advantages and disadvantages of these models are discussed. Determination of the endogenous secretion of the trace element after intravenous injection of its radioisotope may be considered as the simplest and most informative method. (author)

  11. Determination of trace elements in biological material by neutron activation analysis. [As,Au,Br,Cd,Cl,Co,Cr,Fe,Hg,K,Mn,Na,Ni,Rb,Sb,Sc,Se,Zn

    Energy Technology Data Exchange (ETDEWEB)

    Tran Van, L; Teherani, D K

    1989-04-10

    Eighteen trace elements in biological materials (grass (Imperata cylindrica), mimosa plant (Mimosa pudica), rice) by neutron activation method were determined. In the comparative analysis the content of the same element was different in each material, although they were collected at the same place and the same sampling method was applied. (author) 4 refs.; 1 fig.; 1 tab.

  12. Subcellular trace element distribution in Geosiphon pyriforme

    International Nuclear Information System (INIS)

    Maetz, Mischa; Schuessler, Arthur; Wallianos, Alexandros; Traxel, Kurt

    1999-01-01

    Geosiphon pyriforme is a unique endosymbiotic consortium consisting of a soil dwelling fungus and the cyanobacterium Nostoc punctiforme. At present this symbiosis becomes very interesting because of its phylogenetic relationship to the arbuscular mycorrhizal (AM) fungi. Geosiphon pyriforme could be an important model system for these obligate symbiotic fungi, which supply 80-90% of all land plant species with nutrients, in particular phosphorous and trace elements. Combined PIXE and STIM analyses of the various compartments of Geosiphon give hints for the matter exchange between the symbiotic partners and their environment and the kind of nutrient storage and acquisition, in particular related to nitrogen fixation and metabolism. To determine the quality of our PIXE results we analysed several geological and biological standards over a time period of three years. This led to an overall precision of about 6% and an accuracy of 5-10% for nearly all detectable elements. In combination with the correction model for the occurring mass loss during the analyses this holds true even for biological targets

  13. Subcellular trace element distribution in Geosiphon pyriforme

    Energy Technology Data Exchange (ETDEWEB)

    Maetz, Mischa E-mail: mischa.maetz@mpi-hd.mpg.de; Schuessler, Arthur; Wallianos, Alexandros; Traxel, Kurt

    1999-04-02

    Geosiphon pyriforme is a unique endosymbiotic consortium consisting of a soil dwelling fungus and the cyanobacterium Nostoc punctiforme. At present this symbiosis becomes very interesting because of its phylogenetic relationship to the arbuscular mycorrhizal (AM) fungi. Geosiphon pyriforme could be an important model system for these obligate symbiotic fungi, which supply 80-90% of all land plant species with nutrients, in particular phosphorous and trace elements. Combined PIXE and STIM analyses of the various compartments of Geosiphon give hints for the matter exchange between the symbiotic partners and their environment and the kind of nutrient storage and acquisition, in particular related to nitrogen fixation and metabolism. To determine the quality of our PIXE results we analysed several geological and biological standards over a time period of three years. This led to an overall precision of about 6% and an accuracy of 5-10% for nearly all detectable elements. In combination with the correction model for the occurring mass loss during the analyses this holds true even for biological targets.

  14. Trace elements record complex histories in diogenites

    Science.gov (United States)

    Balta, J. B.; Beck, A. W.; McSween, H. Y.

    2012-12-01

    Diogenite meteorites are cumulate rocks composed mostly of orthopyroxene and chemically linked to eucrites (basaltic) and howardites (brecciated mixtures of diogenites and eucrites). Together, they represent the largest single family of achondrite meteorites delivered to Earth, and have been spectrally linked to the asteroid 4 Vesta, the largest remaining basaltic protoplanet. However, this spectral link is non-unique as many basaltic asteroids likely formed and were destroyed in the early solar system. Recent work suggested that Vesta may be an unlikely parent body for the diogenites based on correlations between trace elements and short-lived isotope decay products, which would be unlikely to survive on a body as large as Vesta due to its long cooling history [1]. Recent analyses of terrestrial and martian olivines have demonstrated that trace element spatial distributions can preserve evidence of their crystallization history even when major elements have been homogenized [2]. We have mapped minor elements including Cr, Al, and Ti in seemingly homogeneous diogenite orthopyroxenes and found a variety of previously unobserved textures. The pyroxenes in one sample (GRA 98108) are seemingly large grains of variable shapes and sizes, but the trace elements reveal internal grain boundaries between roughly-equal sized original subgrains, with equilibrated metamorphic triple junctions between them and trace element depletions at the boundaries. These trends suggest extraction of trace elements by a magma along those relict grain boundaries during a reheating event. Two other samples show evidence of fracturing and annealing, with trace element mobility within grains. One sample appears to have remained a closed system during annealing (MET 01084), while the other has interacted with a fluid or magma to move elements along annealed cracks (LEW 88679). These relict features establish that the history of diogenite pyroxenes is more complex than their homogeneous major

  15. Trace Elements in Human Nutrition and Health

    African Journals Online (AJOL)

    Trace Elements in Human Nutrition and Health, a report of a. World Heatth Organisation Expert Committee, contains material contributed by numerous experts consulted in different specialised fields, together with the conClusions reached and recommendations made by the Expert. Consultation. The nineteen nutritionally ...

  16. Trace elements in wine and other beverages

    International Nuclear Information System (INIS)

    Eschnauer, H.

    1974-01-01

    Survey of the mostly physical methods of analysis (e.g. activation analysis) for the dectection of trace elements in wine and in other alcoholic and non-alcoholic beverages as well as for detection of radioactivity (natural and man-made) in these beverages. (HP) [de

  17. Trace and ultratrace level elemental and speciation analysis

    International Nuclear Information System (INIS)

    Arunachalam, J.

    2012-01-01

    Accurate determination of elements present at parts per million and billion levels in various matrices is a growing requirement in different fields. In environmental sciences various trace elements need to be analyzed so as establish the dispersal models of pollutants or the adequacy of effluent treatment prior to discharge into water bodies. The issues of bioaccumulation and magnification are important in aquatic systems. In nutrition and biochemistry one has to establish the bio-availability of essential and toxic elemental species as toxic elements prevent assimilation of essential elements. Fission and fusion technologies use a variety of structural materials requiring many trace elements to be present at levels strictly below the specified levels. Ultra-pure bulk semiconductor materials are required for fabrication devices. In metallurgy and materials sciences too, various trace elements are known to influence the properties. In the emerging fields like nanotechnology, it is necessary to understand the passage and accumulation of nano-particles inside the cells, through trace analysis. Many analytical techniques exist which can provide the concentration information in the bulk materials with good accuracy. They include ICP-AES, FAAS, and ICP-MS, which are solution based techniques. Direct solid state analytical techniques are Glow Discharge Mass Spectrometry (GDMS) and XRF. Accelerator based ion-beam analysis techniques can provide information on concentration and depth profiles of different elements in layered structures. Hyphenated techniques such as HPLC/lC-ICPMS, are helpful in identifying various chemical oxidation states in which a given element might be present in a matrix, which is termed as speciation analysis. This presentation will include the existing analytical competencies and the laboratory requirements for trace and ultra trace element elemental and speciation analyses and their applications. (author)

  18. Simultaneous determination of macro and trace elements in biological reference materials by microwave induced plasma optical emission spectrometry with slurry sample introduction

    International Nuclear Information System (INIS)

    Matusiewicz, Henryk; Golik, Bartosz

    2004-01-01

    A slurry sampling technique (SST) has been utilized for simultaneous multi-element analysis by microwave-induced plasma optical emission spectrometry (MIP-OES). Slurry samples from a spray chamber are fed directly into the microwave cavity-torch assembly (power 300 W) with no desolvation apparatus. The performance of SST-MIP-OES was demonstrated by the determination of macro (Na, K, Ca, Mg, P) and trace (Cd, Cu, Mn, Sr, Zn) elements in three biological certified reference materials using a V-groove, clog-free Babington-type nebulizer. Slurry concentrations up to 1% m/v (particles 3 (pH 1.2) containing 0.01% of Triton X-100, were used with calibration by the standard additions method. The method offers relatively good precision (R.S.D. ranged from 7 to 11%) with measured concentrations being in satisfactory agreement with certified values for NRCC TORT-1 (Lobster hepatopancreas), NRCC LUTS-1 (Lobster hepatopancreas) and IAEA-153 (Milk powder). The concentrations of Na, K, Ca, Mg, P and Cd, Cu, Mn, Sr, Zn were determined in the range 90-22 000 μg/g and 1-420 μg/g, respectively. The method could be useful as a routine procedure

  19. Simultaneous determination of macro and trace elements in biological reference materials by microwave induced plasma optical emission spectrometry with slurry sample introduction

    Energy Technology Data Exchange (ETDEWEB)

    Matusiewicz, Henryk E-mail: Henryk.Matusiewicz@put.poznan.pl; Golik, Bartosz

    2004-05-21

    A slurry sampling technique (SST) has been utilized for simultaneous multi-element analysis by microwave-induced plasma optical emission spectrometry (MIP-OES). Slurry samples from a spray chamber are fed directly into the microwave cavity-torch assembly (power 300 W) with no desolvation apparatus. The performance of SST-MIP-OES was demonstrated by the determination of macro (Na, K, Ca, Mg, P) and trace (Cd, Cu, Mn, Sr, Zn) elements in three biological certified reference materials using a V-groove, clog-free Babington-type nebulizer. Slurry concentrations up to 1% m/v (particles <20 {mu}m), prepared in 10% HNO{sub 3} (pH 1.2) containing 0.01% of Triton X-100, were used with calibration by the standard additions method. The method offers relatively good precision (R.S.D. ranged from 7 to 11%) with measured concentrations being in satisfactory agreement with certified values for NRCC TORT-1 (Lobster hepatopancreas), NRCC LUTS-1 (Lobster hepatopancreas) and IAEA-153 (Milk powder). The concentrations of Na, K, Ca, Mg, P and Cd, Cu, Mn, Sr, Zn were determined in the range 90-22 000 {mu}g/g and 1-420 {mu}g/g, respectively. The method could be useful as a routine procedure.

  20. Studies of trace element determinations in nails by neutron activation analysis method; Estudo de elementos traco em unhas pelo metodo de analise por ativacao com neutrons

    Energy Technology Data Exchange (ETDEWEB)

    Aguiar, Amilton Reinaldo; Saiki, Mitiko [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)

    1996-07-01

    The purpose of this work was to develop the neutron activation analysis for trace element determinations in nails in order to apply this method to the study of the cystic fibrosis disease. It was verified that the elements Al, As, Br, Ca, Cd, Cl, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Se and Zn can be determined by using short and long irradiations with thermal neutron flux from 10{sup 11} to 10{sup 13} n.cm{sup -2}.{sup -1} at the IEA-R1 nuclear research reactor. The washing solutions of triton-X100, NH{sub 4} OH and acetone were tested in order to eliminate external contaminants from the nail samples. The nail analyses of the individual fingers from both of hands showed that the samples must be collected from all the fingers from both of hands to have a representative sample. The precision and the accuracy of the results were also examined by analyzing NIES 10C Rice Flour, IUPAC Bowen's Kale and NIST 1572 Citrus Leaves reference materials. (author)

  1. Application of different methodologies in the preparation of organic matrices for determination of trace elements by differential pulse anodic stripping voltammetry

    International Nuclear Information System (INIS)

    Sisti, Cristina

    2001-01-01

    The determination of trace elements in food samples is of great importance for the human health, considering the factors of essentiality and toxicity. On the other hand, the chemical analysis is largely affected for the steps of sample preparation; laboratory contamination of the sample and the reagents or still volatilization and losses of the elements. If these parameters are not controlled the achieved precision and accuracy could be low. In this work, the content of zinc, cadmium, lead and copper was determined in adults diet samples collected by duplicate portion technique and bovine liver, applying the differential pulse anodic stripping voltametry - (DP-ASV) technique. In the digestion of the matrices in acid medium, conventional methodologies were used, conductive heating in open recipients and equipment with microwaves source in open and closed vessels. The best procedure was the sample digestion by microwaves, in closed vessels and the other treatments made in controlled atmosphere with hood laminar-airflow class 100. The established methodology was validated with the use of a certified sample as reference (NIST - bovine liver 1577b). (author)

  2. Relationship between trace element content in human organs and hair

    International Nuclear Information System (INIS)

    Kinova, L.

    1993-01-01

    Autopsy samples from 22 clinically healthy human males between the ages of 20 to 52 were collected from Bulgaria for the investigation of possible correlations between trace elements in hair and body organs. Samples of heart, spleen, liver, kidney, and hair were analyzed by neutron activation analysis to determine trace element concentrations. Statistical analysis of the data did not indicate any significant correlations between elemental concentrations in hair and internal organs, probably due to the limited number of available samples. However, lower than normal selenium concentrations were found in the organ samples, indicating possible selenium deficiency. (author). 6 refs, 4 tabs

  3. Trace elements in coloured opals using neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    McOrist, G.D.; Smallwood, A. [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia)

    1996-12-31

    Neutron activation analysis (NAA) is a technique particularly suited to analysing opals since it is non-destructive and the silica matrix of opals is not prone to significant activation. It was used to determine the concentration of trace elements in 50 samples of orange, yellow, green, blue and pink opals as well as 18 samples of colourless opals taken from a number of recognised fields in Australia, Peru, Mexico and USA. The results were then evaluated to determine if a relationship existed between trace element content and opal colour. The mean concentration of most of the elements found in orange, yellow and colourless opals were similar with few exceptions. This indicated that, for these samples, colour is not related to the trace elements present. However, the trace element profile of the green, pink and blue opals was found to be significantly different with each colour having a much higher concentration of certain trace elements when compared with all other opals analysed. 7 refs.

  4. Trace elements in coloured opals using neutron activation analysis

    International Nuclear Information System (INIS)

    McOrist, G.D.; Smallwood, A.

    1996-01-01

    Neutron activation analysis (NAA) is a technique particularly suited to analysing opals since it is non-destructive and the silica matrix of opals is not prone to significant activation. It was used to determine the concentration of trace elements in 50 samples of orange, yellow, green, blue and pink opals as well as 18 samples of colourless opals taken from a number of recognised fields in Australia, Peru, Mexico and USA. The results were then evaluated to determine if a relationship existed between trace element content and opal colour. The mean concentration of most of the elements found in orange, yellow and colourless opals were similar with few exceptions. This indicated that, for these samples, colour is not related to the trace elements present. However, the trace element profile of the green, pink and blue opals was found to be significantly different with each colour having a much higher concentration of certain trace elements when compared with all other opals analysed. 7 refs

  5. Trace elements in coloured opals using neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    McOrist, G D; Smallwood, A [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia)

    1997-12-31

    Neutron activation analysis (NAA) is a technique particularly suited to analysing opals since it is non-destructive and the silica matrix of opals is not prone to significant activation. It was used to determine the concentration of trace elements in 50 samples of orange, yellow, green, blue and pink opals as well as 18 samples of colourless opals taken from a number of recognised fields in Australia, Peru, Mexico and USA. The results were then evaluated to determine if a relationship existed between trace element content and opal colour. The mean concentration of most of the elements found in orange, yellow and colourless opals were similar with few exceptions. This indicated that, for these samples, colour is not related to the trace elements present. However, the trace element profile of the green, pink and blue opals was found to be significantly different with each colour having a much higher concentration of certain trace elements when compared with all other opals analysed. 7 refs.

  6. Compton suppression instrumental neutron activation analysis performance in determining trace- and minor-element contents in foodstuff

    International Nuclear Information System (INIS)

    Freitas, M.C.; Dionisio, I.; Pacheco, A.M.G.; Bacchi, M.A.; Fernandes, E.A.N.; Landsberger, S.; Braisted, J.

    2008-01-01

    In 2003-2004, several food items were purchased from large commercial outlets in Coimbra, Portugal. Such items included meats (chicken, pork, beef), eggs, rice, beans and vegetables (tomato, carrot, potato, cabbage, broccoli, lettuce). Elemental analysis was carried out through INAA at the Technological and Nuclear Institute (ITN, Portugal), the Nuclear Energy Centre for Agriculture (CENA, Brazil), and the Nuclear Engineering Teaching Lab of the University of Texas at Austin (NETL, USA). At the latter two, INAA was also associated to Compton suppression. It can be concluded that by applying Compton suppression (1) the detection limits for arsenic, copper and potassium improved; (2) the counting-statistics error for molybdenum diminished; and (3) the long-lived zinc had its 1115-keV photopeak better defined. In general, the improvement sought by introducing Compton suppression in foodstuff analysis was not significant. Lettuce, cabbage and chicken (liver, stomach, heart) are the richest diets in terms of human nutrients. (author)

  7. Trace elements distribution in bottom sediments from Amazon River estuary

    International Nuclear Information System (INIS)

    Lara, L.B.L.S.; Nadai Fernandes, E. de; Oliveira, H. de; Bacchi, M.A.

    1994-01-01

    The Amazon River discharges into a dynamic marine environment where there have been many interactive processes affecting dissolved and particulate solids, either those settling on the shelf or reaching the ocean. Trace elemental concentration, especially of the rare earth elements, have been determined by neutron activation analysis in sixty bottom sediment samples of the Amazon River estuary, providing information for the spatial and temporal variation study of those elements. (author). 16 refs, 6 figs, 3 tabs

  8. The effects of trace element content on pyrite oxidation rates

    Science.gov (United States)

    Gregory, D. D.; Lyons, T.; Cliff, J. B.; Perea, D. E.; Johnson, A.; Romaniello, S. J.; Large, R. R.

    2017-12-01

    Pyrite acts as both an important source and sink for many different metals and metalloids in the environment, including many that are toxic. Oxidation of pyrite can release these elements while at the same time producing significant amounts of sulfuric acid. Such issues are common in the vicinity of abandoned mines and smelters, but, as pyrite is a common accessory mineral in many different lithologies, significant pyrite oxidation can occur whenever pyritic rocks are exposed to oxygenated water or the atmosphere. Accelerated exposure to oxygen can occur during deforestation, fracking for petroleum, and construction projects. Geochemical models for pyrite oxidation can help us develop strategies to mitigate these deleterious effects. An important component of these models is an accurate pyrite oxidation rate; however, current pyrite oxidation rates have been determined using relatively pure pyrite. Natural pyrite is rarely pure and has a wide range of trace element concentrations that may affect the oxidation rate. Furthermore, the position of trace elements within the mineral lattice can also affect the oxidation rate. For example, elements such as Ni and Co, which substitute into the pyrite lattice, are thought to stabilize the lattice and thus prevent pyrite oxidation. Alternatively, trace elements that are held within inclusions of other minerals could form a galvanic cell with the surrounding pyrite, thus enhancing pyrite oxidation rates. In this study, we present preliminary analyses from three different pyrite oxidation experiments each using natural pyrite with different trace element compositions. These results show that the pyrite with the highest trace element concentration has approximately an order of magnitude higher oxidation rate compared to the lowest trace element sample. To further elucidate the mechanisms, we employed microanalytical techniques to investigate how the trace elements are held within the pyrite. LA-ICPMS was used to determine the

  9. Transport of trace elements through the hyphae of an arbuscular mycorrhizal fungus into marigold determined by the multitracer technique

    International Nuclear Information System (INIS)

    Suzuki, H.; Kumagai, H.; Oohashi, K.; Sakamoto, K.; Inubushi, K.; Enomoto, S.

    2001-01-01

    The contribution of the hyphae of an arbuscular mycorrhizal (AM) fungus to the uptake of traceelements by marigold (Tagetes patula L.) was studied using a multitracer consisting of radionuclides of 7 Be, 22 Na, 46 Sc, 51 Cr, 54 Mn, 59 Fe, 56 Co, 65 Zn, 75 Se, 83 Rb, 85 Sr, 88 Y, 88 Zr, and 95m Tc. Marigold plants colonized and not colonized with Glomus etunicatum were grown for 40 and 60 d in pots with a hyphal compartment separated from the rooting medium by a fine nylon mesh. The multitracer was applied to the hyphal compartment. We found that the uptake of 22 Na, 65 Zn , 75 Se, 83 Rb, 85 Sr, and 88 Y by the mycorrhizal plants was higher than that by the non-mycorrhizal ones. In the case of 95m Tc, the uptake by the mycorrhizal plants was similar to that by the control ones. The radioactivity of 7 Be, 46 Sc, 51 Cr, 54 Mn, 59 Fe, 56 Co, and 88 Zr could not be detected in any plants. Our results suggest that the AM fungus can absorb Na, Zn, Se, Rh, Sr, and Y from the soil and transport these elements to the plant through its hyphae. The transport ability of the AM fungal hyphae to plant for Be, Sc, Cr, Mn, Fe, Co, Zr, and Tc is likely to be low. (author)

  10. PIXE trace element analysis of a selection of wines

    International Nuclear Information System (INIS)

    Houdayer, A.; Hinrichsen, P.F.; Martin, J.P.; Belhadfa, A.

    1987-01-01

    The University of Montreal EN Tandem accelerator and a Si (Li) X-ray detector were used for a PIXE (Proton Induced X-ray emission) trace element analysis of a selection of wines. Quantitative measurements of the concentrations of the sixteen trace elements Na, Mg, Al, Si, P, S, Cl, K, Ca, Cr, Mn, Fe, Co, Cu, Zn, and Br were made. To optimize the sensitivity, spectra were recorded at 1.0 MeV proton energy for elements with Z 19. The absolute concentrations of the trace elements were determined by doping the samples of wine with 1000 ppm of vanadium for the 1.0 MeV bombardments, and 1000 ppm of yttrium for the 3.0 MeV irradiations. The targets were prepared by depositing a few microliters of the wine onto a Nuclepore filter

  11. Report on the quality control study NAT-7 for the determination of trace and minor elements in dust artificially loaded on air filters

    International Nuclear Information System (INIS)

    Bleise, A.; Smodis, A.

    2002-02-01

    from the literature. Precision and accuracy criteria were applied to 10 elements. 350 laboratory mean values were reported for these elements, 75 values (21%) did not pass the set proficiency test criteria. The individual laboratory results are listed in appendix IV. In conclusion, the results from this quality control study revealed that the determination of trace elements in dust material loaded on filters is a difficult task for analytical laboratories. The results indicate the urgent need for a real matrix standard reference material for checking and improving the analytical performance in laboratories analysing routinely air filters (author)

  12. Using the ion microprobe mass analyser for trace element analysis

    International Nuclear Information System (INIS)

    Schilling, J.H.

    1978-01-01

    Most techniques for the analysis of trace elements are capable of determining the concentrations in a bulk sample or solution, but without reflecting their distribution. In a bulk analysis therefore elements which occur in high concentration in a few precipitates would still be considered trace elements even though their local concentration greatly exceed the normally accepted trace elements concentration limit. Anomalous distribution is also shown by an oxide layer, a few hundred Angstrom thick, on an aluminium sample. A low oxide concentration would be reported if it were included in the bulk analysis, which contradicts the high surface concentration. The importance of a knowledge of the trace element distribution is therefore demonstrated. Distributional trace element analysis can be carried out using the ion microprobe mass analyser (IMMA). Since the analytical technique used in this instrument, namely secondary ion mass spectrometry (SIMS), is not universally appreciated, the instrument and its features will be described briefly followed by a discussion of quantitative analysis and the related subjects of detection limit and sample consumption. Finally, a few examples of the use of the instrument are given

  13. Determination of minor and trace elements in aromatic spices by micro-wave assisted digestion and inductively coupled plasma-mass spectrometry.

    Science.gov (United States)

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

    2014-09-01

    This study aimed at analyzing the concentrations of 23 minor and trace elements in aromatic spices by inductively coupled plasma-mass spectrometry (ICP-MS), after wet digestion by microwave system. The analytical method was validated by linearity, detection limits, precision, accuracy and recovery experiments, obtaining satisfactory values in all cases. Results indicated the presence of variable amounts of both minor and trace elements in the selected aromatic spices. Manganese was high in cinnamon (879.8 μg/g) followed by cardamom (758.1 μg/g) and clove (649.9 μg/g), strontium and zinc were high in ajwain (489.9 μg/g and 84.95 μg/g, respectively), while copper was high in mango powder (77.68 μg/g). On the whole some of the minor and essential trace elements were found to have good nutritional contribution in accordance to RDA. The levels of toxic trace elements, including As, Cd, and Pb were very low and did not found to pose any threat to consumers. Copyright © 2014 Elsevier Ltd. All rights reserved.

  14. High-pressure liquid chromatography of trace elements: Determination of terbium in terbium doped gadolinium oxide sulphide phosphors

    International Nuclear Information System (INIS)

    Mazzucotelli, A.; Dadone, A.; Frache, R.; Baffi, F.; Genoa Univ.

    1982-01-01

    A detailed study of isocratic and gradient elution separations of lanthanides has been carried out. Analyses of industrially and scientifically interesting products such as luminescent phosphors have been carried out by gradient elution with DL-2-hydroxyisobutyric acid. The determination of small amounts of terbium in gadolinium oxide sulphide phosphors is described in which an HCl solution was eluted through a stainless steel column packed with microparticulate silica, with bonded cation-exchange groups. Complete separation of gadolinium and terbium is achieved. Detection is with a variable wavelength detector following post-column complex formation with 4-(2-pyridylazo)-resorcinol monosodium salt. Results obtained on test solutions show good reproducilbity and sensitivtiy and the method may be considered sufficiently reliable to be used in routine quality control procedures. (orig.)

  15. Trace elements and protein in human milk

    International Nuclear Information System (INIS)

    Abusamra, Y.I.H.

    1995-01-01

    The trace elements Zn, Fe, Cu, Mn, Ni and Pb and some related major elements which are Ca, Cl K and total protein contents of human samples from ninety mothers were examined in this study. Samples were collected from Khartoum, Khartoum North and Omdurman, from the second day of delivery up to the third month where the milk reaches a relatively stable levels. These samples representing different stages of lactation which are colostrum ( 1-3 days ), tranitional ( up to 14 days ) and mature milk. The principle aim of this study is to measure the trace elements and protein contents in relation to stage of lactation and to compare with the literature. Atomic absorption spectroscopy and X-ray fluorescence were used to measure trace elements in the samples. The methods were found to be quite reliable as proved by the analysis of the standard reference material HM-1. Whereas neutron activation analysis was used for measurements of total protein. Colostrum was found to have the highest amounts of trace elements and protein. Fe mean concentration was 273 g/dm 3 at colostrum stage and it decreased to 146 g/dm 3 in mature milk ( 49% ). Zn decreased from 6000 g/dm 3 in colostrum to 1300 g/dm 3 in mature stage ( 78% ). Mn was 12g/dm 3 in colostrum, and it decreased to 2.9 g/dm 3 in mature milk ( 75% ). Cu decreased from 370 g/dm 3 to 117 g/dm 3 ( 68% ). Ni decreased from 24 g/dm 3 to 8.8 g/dm 3 ( 63% ) and Pb from 12 g/dm 3 to 2.6 g/dm 3 ( 76% ). Total protein was 37.3% of the dry milk in colostrum and it was 12.2% in mature milk. (author). 75 refs., 25 tabs., 30 figs

  16. Socio-demographic, lifestyle, and dietary determinants of essential and possibly-essential trace element levels in adipose tissue from an adult cohort.

    Science.gov (United States)

    Rodríguez-Pérez, Celia; Vrhovnik, Petra; González-Alzaga, Beatriz; Fernández, Mariana F; Martin-Olmedo, Piedad; Olea, Nicolás; Fiket, Željka; Kniewald, Goran; Arrebola, Juan P

    2018-05-01

    There is increasing evidence linking levels of trace elements (TEs) in adipose tissue with certain chronic conditions (e.g., diabetes or obesity). The objectives of this study were to assess concentrations of a selection of nine essential and possibly-essential TEs in adipose tissue samples from an adult cohort and to explore their socio-demographic, dietary, and lifestyle determinants. Adipose tissue samples were intraoperatively collected from 226 volunteers recruited in two public hospitals from Granada province. Trace elements (Co, Cr, Cu, Fe, Mn, Mo, Se, V, and Zn) were analyzed in adipose tissue by high-resolution inductively coupled plasma mass spectrometry (HR-ICP-MS). Data were collected on socio-demographic characteristics, lifestyle, diet, and health status by face-to-face interview. Predictors of TE concentrations were assessed by using multivariable linear and logistic regression. All TEs were detected in all samples with the exception of Se (53.50%). Iron, zinc, and copper showed the highest concentrations (42.60 mg/kg, 9.80 mg/kg, and 0.68 mg/kg, respectively). Diet was the main predictor of Cr, Fe, Mo, and Se concentrations. Body mass index was negatively associated with all TEs (β coefficients = -0.018 to -0.593, p = 0.001-0.090) except for Mn and V. Age showed a borderline-significant positive correlation with Cu (β = 0.004, p = 0.089). Residence in a rural or semi-rural area was associated with increased Co, Cr, Fe, Mo, Mn, V and Zn concentrations and with β coefficients ranging from 0.196 to 0.544 (p V concentrations (β coefficients = 0.276-0.368, p = 0.022-0.071). This is the first report on the distribution of these TEs in adipose tissue and on their determinants in a human cohort and might serve as an initial step in the elucidation of their clinical relevance. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Assessment of trace element stabilization in soil

    OpenAIRE

    Kumpiene, Jurate

    2005-01-01

    The thesis deals with the remediation of trace element contaminated soil by the chemical stabilization technique. The objective is to complement the knowledge about possibilities of applying the stabilization either (1) as an alternate soil remediation method to excavation and landfilling or (2) for a pre-treatment of contaminated soil before landfilling. The work is based on two case studies of the stabilization of 1) Cr, Cu, As, and Zn contaminated soil using metallic iron and 2) Pb and Cu ...

  18. Trace-element analysis in environmental sciences

    International Nuclear Information System (INIS)

    Valkovic, V.; Moschini, G.

    1988-01-01

    The use of charged-particle accelerators in trace-element analysis in the field of environmental sciences is described in this article. Nuclear reactions, charged-particle-induced X-ray emission as well as other nuclear and atomic processes can be used individually, or combined, in developing adequate analytical systems. In addition to concentration levels, concentration levels, concentration profiles can be measured, resulting in unique information. Some examples of experiments performed are described together with the suggestions for future measurements [pt

  19. Development of methods for the neutron activation analysis to the determination of essential and toxic trace elements of biological and environmental samples: application of enzyme activity of raw hides

    International Nuclear Information System (INIS)

    Sipos, T.; Nagy, L.G.; Toeroek, G.; Kollar, J.

    1974-01-01

    Investigations on the post mortem enzymatic processes pointed out the fact, that significant deviations can be observed in the extent and in the results of the autolytic transformations occurring during the storage of raw hide. A neutron activation analysis procedure, based on a semiautomated radiochemical separation procedure and scintillation gamma spectrometry, was selected for the determination of some trace elements. Six trace elements, Cu, Mn, Zn, Au, As, and Cr, and one minor component,Br, were detected and/or determined in the concentration region of 0,1-10 3 ppM. According to preliminary investigations evaluated at the time being, concentration differences of some orders of magnitude were obtained for some trace elements: copper, zinc and manganese, whereas the concentration of bromine remained practically constant. These findings seem to correlate with large differences in appearance due to different enzyme activities in the raw hides

  20. Dietary patterns and trace elements intake evaluation

    International Nuclear Information System (INIS)

    Rahman, A.; Waheed, S.; Zaidi, J.H.; Ahmad, S.

    1998-01-01

    The dietary patterns and trace element contents of the integrated diets of middle income population in Gujranwala and of Islamabad have been studied and dietary intake of winter and summer are given. An overview of the elemental concentration in the two sets of integrated diets reveals similar zinc and manganese concentrations; comparatively higher nickel, selenium and potassium concentrations in Gujranwala and higher chromium, cesium, scandium, sodium and chlorine concentrations in Islamabad. These results undoubtedly reflect the difference in food selection and habits of the two populations, the influence of soil content and industrial pollution

  1. Trace Elements in Teeth by ICPMS

    International Nuclear Information System (INIS)

    Zahran, N.F.; Helal, A.I.; Amr, M.A.; Amr, M.A.; Al-saad, K.A.

    2008-01-01

    Teeth are reported to be suitable indicators of trace element exposure from environment and nutritional status. Inductively coupled plasma mass spectrometry (ICP-MS) is used to compare the trace element content of children's primary teeth and adult teeth. Primary teeth are collected from 28 children and 42 adult from non-industrial City. The data are assessed statistically using t-tests. The adult teeth contained significantly greater concentrations of Na, Mg, Al, Fe, Ni, Cu, Sr, Cd, Ba, Pb and U and significantly less Mn, Co, As, Se, Mo and Bi than the children teeth. Additional measurements on adult teeth pulps are performed. Comparison between trace element concentrations in health and caries teeth pulps show that the mean concentrations of Na, Al, K, Cr, Mn, Co, Cu, Zn, Mo, Ag, Bi and U are lower in caries than healthy teeth pulps. On the other hand, the mean concentrations of Mg, Cd and Pb are higher in caries samples than healthy teeth pulps

  2. Trace elements in termites by PIXE analysis

    Energy Technology Data Exchange (ETDEWEB)

    Yoshimura, T. E-mail: tsuyoshi@termite.kuwri.kyoto-u.ac.jp; Kagemori, N.; Kawai, S.; Sera, K.; Futatsugawa, S

    2002-04-01

    Trace elements in a Japanese subterranean xylophagous termite, Coptotermes formosanus Shiraki, were analyzed by the PIXE method. The total amount of the 14 predominant elements out of 27 detected in an intact termite was higher in a soldier termite (23 000 {mu}g/g) than in a worker termite (10 000 {mu}g/g). A block of wood (Pinus densiflora Sieb. et Zucc.) for termite feed had a much lower concentration (3600 {mu}g/g) compared with that in an intact termite. This probably relates the functional bio-condensation and/or bio-recycling of trace elements in C. formosanus. When a termite was separated into three anatomical parts, head, degutted body and gut, the worker gut contained the highest total amount of the 14 predominant measured elements (31 000 {mu}g/g). This might be correlated with the higher activity of food digestion and energy production in the worker gut. Moreover, the mandible of the soldier head, with an exoskeleton that is intensely hardened, showed a preferential distribution of Mn and Fe. These results suggest that the characteristic localization of elements will be closely related to the functional role of the individual anatomical part of C. formosanus.

  3. Neutron activation analysis of trace elements in foodstuffs

    International Nuclear Information System (INIS)

    Schelenz, R.; Fischer, E.

    1976-05-01

    A neutron activation method for multielement determination in biological material was developed. The individual steps of the method include radiochemical processing as well as nondestructive techniques. In order to develop a high resolution gamma spectrometric method the indispensable assumptions were the application of Ge(Li)-semiconductor detectors, multi-channel pulse height analyzers and the use of electronic data evaluation with mini-computers for the automatic evaluation of complex gamma spectra. After radiochemical separation (RNAA) 33 elements can be determined in biological materials and by application of nondestructive, purely instrumental techniques (INAA) 25 elements. The time required for the analysis of 33 elements can be determined in biological materials and by application of nondestructive, purely instrumental techniques (INAA) 25 elements. The time required for the analysis of 33 elements is 4 days. The neutron activation method is used routinely for the determination of trace elements in foodstuffs and in the field of nutrition research. (orig.) [de

  4. Trace element analysis in rheumatoid arthritis under chrysotherapy

    International Nuclear Information System (INIS)

    Lecomte, R.; Paradis, P.; Monaro, S.; Barrette, M.; Lamoureux, G.; Menard, H.A.

    1981-01-01

    Proton induced X-ray emission (PIXE) analysis is used to measure trace element concentrations in blood serum from patients with rheumatoid arthritis. Initially trace element contaminations in blood-collecting and storing devices are determined. Then mean values and nyctemeral cycles are measured both in normal subjects and patients with rheumatoid arthritis and other similar pathologies. Abnormal concentrations of Cu and Zn and anomalies in the nyctemeral cycle are found in the patients. In the second phase of the project, the special case of chrysotherapeutically treated (gold salt treatment) rheumatoid arthritis patients is studied for extended periods of time (up to 53 weeks). (orig.)

  5. Trace elements distribution in the Amazon floodplain soils

    International Nuclear Information System (INIS)

    Fernandes, E.A.N.; Ferraz, E.S.B.; Oliveira, H.

    1994-01-01

    Neutron activation analysis was performed on aluvial soil samples from several sites on the foodplains of the Amazon River and its major tributaries for trace elements determination. The spatial and temporal variations of chemical composition of floodland sediments in the Amazon basin are discussed. No significant difference was found in trace elemental distribution in the floodland soils along the Amazon main channel, even after the source material has been progressively diluted with that from lowland draining tributaries. It was also seen that the average chemical composition of floodplain soils compares well with that of the suspended sedimets. (author) 12 refs.; 5 figs.; 2 tabs

  6. Identifying sources of groundwater pollution using trace element signatures

    International Nuclear Information System (INIS)

    Olmez, I.; Hayes, M.J.

    1990-01-01

    A simple receptor modeling approach has been applied to groundwater pollution studies and has shown that marker trace elements can be used effectively in source identification and apportionment. Groundwater and source materials from one coal-fired and five oil-fired power plants, and one coal-tar deposit site have been analyzed by instrumental neutron activation analysis for more than 20 minor and trace elements. In one of the oil-fired power plants, trace element patterns indicated a leak from the hazardous waste surface impoundments owing to the failure of a hypolon liner. Also, the extent and spatial distribution of groundwater contamination have been determined in a coal-tar deposit site

  7. Wet deposition flux of trace elements to the Adirondack region

    International Nuclear Information System (INIS)

    Huang, X.; Keskin, S.S.; Gullu, G.; Olmez, I.

    2001-01-01

    Wet deposition samples from two locations in the Adirondack region of New York were analyzed for trace elemental composition by instrumental neutron activation analysis. Annual fluxes of the measured species were determined by precipitation-weighted and linear-regression methods. Despite several episodes of high deposition fluxes, the cumulative areal wet deposition of trace elements increased fairly linearly (r 2 > 0.9) over the two year sampling period at both sites. This implies that short duration sampling programs may be used to estimate long-term fluxes and cumulative wet deposition impacts. Based on the magnitude of their fluxes, the measured species have been divided into four groups: acidic anions, electroneutral balancing cations, and minor and trace elements of anthropogenic origin. (author)

  8. Uptakes of trace elements in Zn-deficient mice

    International Nuclear Information System (INIS)

    Ohyama, T.; Yanaga, M.; Yoshida, T.; Maetsu, H.; Suganuma, H.; Omori, T.

    2002-01-01

    A multitracer technique was used to obtain uptake rates of essential trace elements in various organs and tissues in Zn-deficient mice. A multitracer solution, containing more than 20 radioisotopes, was injected intraperitoneally into Zn-deficient state mice and control ones. Uptake rates of the radioisotopes were compared with concentrations of trace elements determined by instrumental neutron activation analysis (INAA) in order to study a specific metabolism of Zn and other essential trace elements, such as Mn, Co, Se, Rb, and Sr. The result suggests that Zn is supplied from bone to other organs and tissues and an increase in Co concentration in all organs and tissues depends on its chemical form, under the Z-deficient state. (author)

  9. Environmental lichenology: Biomonitoring of trace element air pollution

    International Nuclear Information System (INIS)

    Sukhodub, L.S.; Sulkio-Cleff, B.

    2001-01-01

    The review of application of lichens and mosses as biomonitors of air pollution have been presented. The neutron activation analysis and atomic absorption spectroscopy have been used for trace element content determination in lichens and mosses taken from different regions of Europe

  10. Effect of soil moisture on trace elements concentrations using ...

    African Journals Online (AJOL)

    Portable X-ray fluorescence (PXRF) technology can offer rapid and cost-effective determination of the trace elements concentrations in soils. The aim of this study was to assess the influence of soil moisture content under different condition on PXRF measurement quality. For this purpose, PXRF was used to evaluate the soil ...

  11. Analysis of Trace Elements in South African Clinkers using Latent ...

    African Journals Online (AJOL)

    The trace element content of clinkers (and possibly of cements) can be used to identify the manufacturing factory. The Mg, Sr, Ba, Mn, Ti, Zr, Zn and V content of clinkers give detailed information for the determination of the origin of clinkers produced in different factories. However, for the analysis of such complex data there ...

  12. Accumulation and bioaccessibility of trace elements in wetland ...

    African Journals Online (AJOL)

    Accumulation of trace metals in sediment can cause severe ecological impacts. In this study, determination of elemental concentrations in water and sediment was done. Shadegan wetland is one of the most important wetlands in southwest of Iran and is among the Ramsar-listed wetlands. Wastewaters from industries ...

  13. Minerals and trace elements in domesticated Namibian Ganoderma ...

    African Journals Online (AJOL)

    The minerals and trace elements in domesticated Namibian Ganoderma mushroom species were determined. The results show that fiber content was found highest with 45 g/100 g of dry weight, followed by calcium with 23 g/100 g, carbohydrate with 23 g/100 g, protein with 18.2 g/100 g, iron with 6.41 g/100 g, copper with ...

  14. The status of trace elements in lymphoma and esophageal cancer ...

    African Journals Online (AJOL)

    Cancer is a life threatening disease. Many people die of cancer every year. Epidemiological studies suggest that alteration of trace elements in the body can contribute to the development of cancer. The aim of this study was to determine the concentration of zinc (Zn), copper (Cu), lead (Pb), Nickel (Ni), iron (Fe) and ...

  15. Horizontal variation in trace elements and soil characteristics at ...

    African Journals Online (AJOL)

    2016-10-04

    Oct 4, 2016 ... Soil indicators – pH, soil organic matter (SOM) and soil water retention (SWR) – were also ... The determination of total extractable trace element concen- ..... Tshipise soil. Factor 1. Factor 2. Factor 1. Factor 2. Li. −0.497. 0.176 ..... KABANDA TA (2003) Climate in A first synthesis of the environmental, bio-.

  16. Trace elements in Taiwanese diet in different seasons

    International Nuclear Information System (INIS)

    Sheng-Ming Liu; Chien Chung

    1992-01-01

    The trace element contents of Taiwanese diet were determined using conventional neutron activation analysis. Sample were prepared with duplicate portion technique by collecting food items ate and drank during a 3 day period in winter. Samples were homogenized, freeze-dried, and elemental concentration of trace elements were determined by instrumental neutron activation analysis. The interference from fast neutron induced reactions were corrected. Concentrations and daily dietary intake of the elements were compared with those collected in the summer, resulting less daily intake of K, Ca, Mn, Fe and Zn among Taiwanese than the values recommended by WHO and RDA. Alarming low intake of Fe for females and Zn among Taiwanese were indicated. (author) 6 refs.; 2 figs.; 5 tabs

  17. Preconcentration and Speciation of Trace Elements and Trace-Element Analogues of Radionuclides by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Chatt, A.

    1999-01-01

    We have developed a number of preconcentration neutron activation analysis (PNAA) methods in our laboratory for the determination of trace elements in a variety of complex sample matrices. We developed a number of cocrystallization and coprecipitation methods for the determination of trace elements in water samples. We developed several methods for the determination of I in foods and diets. We have developed a number of PNAA methods in our laboratory We determined As and Sb in geological materials and natural waters by coprecipitation with Se and Au in silicate rocks and ores by coprecipitation with Te followed by NAA. We developed an indirect NAA method for the determination of B in leachates of borosilicate glass. We have been interested in studying the speciation of Am, Tc, and Np in simulated vitrified groundwater leachates of high-level wastes under oxid and anoxic conditions using a number of techniques. We then used PNAA methods to study speciation of trace-element analogues of radionuclides. We have been able to apply biochemical techniques and NAA for the separation, preconcentration, and characterization of metalloprotein and protein-bound trace-element species in subcellular fractions of bovine kidneys. Lately, we have concentrated our efforts to develop chemical and biochemical methods in conjunction with NAA, NMR, and MS for the separation and identification of extractable organohalogens (EOX) in tissues of beluga whales, cod, and northern pink shrimp

  18. Concentration of trace elements on branded cigarette in Malaysia

    International Nuclear Information System (INIS)

    Azman, Muhammad Azfar; Hamzah, Suhaimi; Rahman, Shamsiah Abdul; Elias, Md Suhaimi; Abdullah, Nazaratul Ashifa; Hashim, Azian; Shukor, Shakirah Abd; Yasir, Muhamad Samudi; Rahman, Irman Abdul

    2016-01-01

    Tobacco is a plant that is used as a recreational drug since the beginning of its use by the Native Americans. Now with the development of the tobacco industry, smoking has become a norm for the public in Malaysia. Trace elements in plants are mostly due to the uptake processes from the soils into the roots of the plants. The concentration of the elements may also be influenced by the elements contained in the water and also fertilizers. This paper aim to analyze the concentration of the trace elements contained in the branded cigarettes sold in Malaysia by utilizing the neutron activation analysis. The tobaccos were taken out from the cigarettes. The collected samples were air dried and passed through 2 mm sieve. Instrumental Neutron Activation Analysis (NAA) has been used for the determination of trace elements. Samples were activated in the Nuclear Malaysia Triga Mark II reactor with a neutron flux of 2.0 x 10 12 n cm -2 s -1 . The samples then were analyzed using ORTEC Gamma Spectrometer a co-axial n-type HPGe detector with resolution of 2.0 keV at 1332 keV and relative efficiency of 20%. The data obtained could help in assessing the concentration of the trace elements that complying with the standard limitation dose proposed by World Health Organization (WHO)

  19. Concentration of trace elements on branded cigarette in Malaysia

    Energy Technology Data Exchange (ETDEWEB)

    Azman, Muhammad Azfar, E-mail: m-azfar@nuclearmalaysia.gov.my; Hamzah, Suhaimi; Rahman, Shamsiah Abdul; Elias, Md Suhaimi; Abdullah, Nazaratul Ashifa; Hashim, Azian; Shukor, Shakirah Abd [Blok 18, Makmal Kimia Analisis (ACA/BAS), Agensi Nuklear Malaysia, 43000 Kajang, Selangor (Malaysia); Yasir, Muhamad Samudi; Rahman, Irman Abdul [Bangunan Sains Nuklear, Fakulti Sains & Teknologi, UKM Bangi, 43600 Bangi, Selangor (Malaysia)

    2016-01-22

    Tobacco is a plant that is used as a recreational drug since the beginning of its use by the Native Americans. Now with the development of the tobacco industry, smoking has become a norm for the public in Malaysia. Trace elements in plants are mostly due to the uptake processes from the soils into the roots of the plants. The concentration of the elements may also be influenced by the elements contained in the water and also fertilizers. This paper aim to analyze the concentration of the trace elements contained in the branded cigarettes sold in Malaysia by utilizing the neutron activation analysis. The tobaccos were taken out from the cigarettes. The collected samples were air dried and passed through 2 mm sieve. Instrumental Neutron Activation Analysis (NAA) has been used for the determination of trace elements. Samples were activated in the Nuclear Malaysia Triga Mark II reactor with a neutron flux of 2.0 x 10{sup 12} n cm{sup -2} s{sup -1}. The samples then were analyzed using ORTEC Gamma Spectrometer a co-axial n-type HPGe detector with resolution of 2.0 keV at 1332 keV and relative efficiency of 20%. The data obtained could help in assessing the concentration of the trace elements that complying with the standard limitation dose proposed by World Health Organization (WHO)

  20. Concentration of trace elements on branded cigarette in Malaysia

    Science.gov (United States)

    Azman, Muhammad Azfar; Yasir, Muhamad Samudi; Rahman, Irman Abdul; Hamzah, Suhaimi; Rahman, Shamsiah Abdul; Elias, Md Suhaimi; Abdullah, Nazaratul Ashifa; Hashim, Azian; Shukor, Shakirah Abd

    2016-01-01

    Tobacco is a plant that is used as a recreational drug since the beginning of its use by the Native Americans. Now with the development of the tobacco industry, smoking has become a norm for the public in Malaysia. Trace elements in plants are mostly due to the uptake processes from the soils into the roots of the plants. The concentration of the elements may also be influenced by the elements contained in the water and also fertilizers. This paper aim to analyze the concentration of the trace elements contained in the branded cigarettes sold in Malaysia by utilizing the neutron activation analysis. The tobaccos were taken out from the cigarettes. The collected samples were air dried and passed through 2 mm sieve. Instrumental Neutron Activation Analysis (NAA) has been used for the determination of trace elements. Samples were activated in the Nuclear Malaysia Triga Mark II reactor with a neutron flux of 2.0 x 1012 n cm-2 s-1. The samples then were analyzed using ORTEC Gamma Spectrometer a co-axial n-type HPGe detector with resolution of 2.0 keV at 1332 keV and relative efficiency of 20%. The data obtained could help in assessing the concentration of the trace elements that complying with the standard limitation dose proposed by World Health Organization (WHO).

  1. Trace element studies at University of Pittsburgh

    International Nuclear Information System (INIS)

    Cohen, B.L.; Chan, K.C.; Shabason, L.; Wedberg, G.; Rudolph, H.

    1974-01-01

    Seven areas of research are discussed. A method was developed for analyzing samples for their major constituent elements by irradiating with protons and detecting prompt gamma rays, mostly produced in (p,p'γ) reactions. Among other applications, the method was used to analyze air particulates for C, N, O, Al, Si, S, Co, and Fe. Trace element analysis by proton or alpha particle induced x-ray fluorescence was used on thin samples in a study of the variations of Pb, Br, Fe, and Zn in air particulates as a function of time. Among other applications this method was also used in studying trace elements in rainwater. An x-ray fluorescence method that is effective in the analysis of thick samples was developed. A method based on measuring energies of elastically scattered protons was developed for the analysis of light elements. The use of proton and neutron activation analyses, as well as methods for studying depth profiles for hydrogen and helium in materials are discussed

  2. Minerals and trace elements determination in diets by neutron activation analysis; Determinacao de elementos minerais e tracos em dietas pela tecnica de ativacao neutronica

    Energy Technology Data Exchange (ETDEWEB)

    Eiras, Maria Izabel O.; Favaro, Debora I.T. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil). Lab. de Analise por Ativacao Neutronica; Ribeiro, Marisilda; Cozzolino, Silvia M.F. [Sao Paulo Univ., SP (Brazil). Dept. de Alimentos e Nutricao Experimental. Lab. de Minerais

    2002-07-01

    In the present study 12 diets, each one consisting of a pool of seven day diets, composed by four meals: breakfast, lunch, dinner and snack, adequate in energy and macro nutrients according to the RDA (Recommended Daily Allowance) recommendations, were elaborated and offered to a group of 12 men (19-42 years). The diets were collected by duplicate portion technique and dried by two different processes: freeze drying and 60 deg C ventilated oven drying. In the total, 24 diets were analyzed. The content of some minerals and trace elements (Ca, Fe, Mg, Mn, Na, Se and Zn) were determined by Instrumental Neutron Activation Analysis. The validation of methodology was made by analysis of the reference materials Typical Diet (NIST SRM 1548{sup a}), Orchard Leaves (NIST SRM 1541) and Peach Leaves (NIST SRM 1547). The results observed by two different drying processes used were statistically compared by test T of Student. It was possible to conclude that the concentration means can be considered as statistically equal, within a significance level of 0.05. The daily intake values calculated from the concentration results were: 712 ({+-} 59) mg Ca/day; 10.7 ({+-} 0.8) mg Fe/ day; 3387 ({+-} 16) mg K/ day; 275 ({+-} 6) mg Mg/ day; 3.0 ({+-} 0.5) mg Mn/ day; 3656 ({+-} 699) mg Na/ day; 42 ({+-} 6) {mu}g Se/ day e 11.6 ({+-} 2.4) mg Zn/ day. The calculated intake was compared to the new daily recommended values set by RDA (National Research Council-USA) for the range age of individuals studied. It was possible to conclude that the diets were adequate in Fe and Zn and inadequate for the other elements. Concerning the minerals Na and K we verified high daily intake levels and this was already observed in other Brazilian regional diets. (author)

  3. Trace element inhibition of phytase activity.

    Science.gov (United States)

    Santos, T; Connolly, C; Murphy, R

    2015-02-01

    Nowadays, 70 % of global monogastric feeds contains an exogenous phytase. Phytase supplementation has enabled a more efficient utilisation of phytate phosphorous (P) and reduction of P pollution. Trace minerals, such as iron (Fe), zinc (Zn), copper (Cu) and manganese (Mn) are essential for maintaining health and immunity as well as being involved in animal growth, production and reproduction. Exogenous sources of phytase and trace elements are regularly supplemented to monogastric diets and usually combined in a premix. However, the possibility for negative interaction between individual components within the premix is high and is often overlooked. Therefore, this initial study focused on assessing the potential in vitro interaction between inorganic and organic chelated sources of Fe, Zn, Cu and Mn with three commercially available phytase preparations. Additionally, this study has investigated if the degree of enzyme inhibition was dependent of the type of chelated sources. A highly significant relationship between phytase inhibition, trace mineral type as well as mineral source and concentration, p phytases for Fe and Zn, as well as for Cu with E. coli and Aspergillus niger phytases. Different chelate trace mineral sources demonstrated diversifying abilities to inhibit exogenous phytase activity.

  4. Determination of trace elements and heavy metals in agricultural products cultivated at the Rimac river valley in Lima city using nuclear and related analytical techniques

    OpenAIRE

    Bedregal, Patricia; Torres, Blanca; Olivera, Paula; Mendoza, Pablo; Ubillús, Marco; Creed-Kanashiro, H.; Penny, M.; Junco, J.; Ganoza, L.

    2004-01-01

    There are strong indications that the Rimac river valley is being contaminated with heavy metals and an excess of trace elements that come from some industrial and mining activities developed along the Rimac river valley. The agricultural products cultivated there in could be suffering the same effect. Nuclear and related analytical techniques will play an important role in the study of pollution by providing information concerning the degree of contamination in some agricultural products cul...

  5. Trace element ink spiking for signature authentication

    International Nuclear Information System (INIS)

    Hatzistavros, V.S.; Kallithrakas-Kontos, N.G.

    2008-01-01

    Signature authentication is a critical question in forensic document examination. Last years the evolution of personal computers made signature copying a quite easy task, so the development of new ways for signature authentication is crucial. In the present work a commercial ink was spiked with many trace elements in various concentrations. Inorganic and organometallic ink soluble compounds were used as spiking agents, whilst ink retained its initial properties. The spiked inks were used for paper writing and the documents were analyzed by a non destructive method, the energy dispersive X-ray fluorescence. The thin target model was proved right for quantitative analysis and a very good linear relationship of the intensity (X-ray signal) against concentration was estimated for all used elements. Intensity ratios between different elements in the same ink gave very stable results, independent on the writing alterations. The impact of time both to written document and prepared inks was also investigated. (author)

  6. Sources of trace elements in total diet. A statistical approach

    International Nuclear Information System (INIS)

    Aras, N.K.; Chatt, A.

    2004-01-01

    Sixteen total diet samples have been collected from two socioeconomic groups in Turkey by duplicate portion techniques. Samples were homogenized with titanium-blade homogenizer, freeze dried and analyzed for their minor and trace elements mostly by neutron activation analysis. Bread and flour samples were also collected from the same regions and analyzed similarly by instrumental neutron activation analysis. Concentrations of more than 25 elements in total diets, bread and flour, and fiber and phytate in total diets have been determined. Daily dietary intakes of these population groups, probable source of elements through correlation coefficients, and enrichment factor calculations have been determined. (author)

  7. Determination of uranium isotopes (235U, 238U) and trace elements (Cd, Pb, Cu and As) in bottled drinking water by Icp-SFMS

    International Nuclear Information System (INIS)

    Lara A, N.; Hernandez M, H.; Romero G, E. T.; Kuri de la C, A.; Perez B, M. A.

    2016-09-01

    In the present work we propose an optimized method for the quantification of uranium isotopes ( 235 U, 2 38 U) and the elements Cd, Pb, Cu and As in bottled water for drinking at trace levels of concentration. Based on the multi-element detection capability, the high sensitivity and resolution that the Mass Spectrometry with Magnetic Sector with Inductively Coupled Plasma Source (Icp-SFMS) technique offers; the high, medium and low resolution analysis conditions for the elements under study were established and optimized using and Element 2/Xr equipment and the 23 multi-elemental Certified Reference Material (CRM). The analysis method was validated using the standard reference material Nist 1643d and CRM mono-elemental s as external standards for the quantification of the analytes. Samples, targets and CRM were acidified with 2% of HNO 3 and analyzed without pretreatment under the established analysis conditions. The results obtained show concentrations of 235 U, 238 U, 111 Cd, 208 Pb, 63 Cu and 75 As in the range of μg L -1 , the linearity obtained from the calibration curves for each element has correlation coefficients < 0.99 in all cases, the accuracy of the method in terms of percent relative standard deviation (RSD %) was less than 5%, the mean recovery rate of Nist 1643d ranged from 96.46% to 101.12%. The optimization of the method guarantees the stability and calibration of the equipment throughout the analysis, as well as the ability to resolve interferences. In conclusion, the method proposed using Icp-SFMS offers the advantages of being fast and simple for the multi-elemental analysis in water at trace levels, with low limits of quantification and detection, with good linearity, accuracy, precision and reproducibility to a degree of reliability of 95%. (Author)

  8. Reply to the Comment by A. Wyttenbach and L. Tobler and correction for errata on 'Minor and trace element determination of food spices and pulses of different origins by NAA and PAA'

    International Nuclear Information System (INIS)

    Miyamoto, Y.; Kajikawa, A.; Zaidi, J.H.; Nakanishi, T.; Sakamoto, K.; Kanazawa Univ.

    2001-01-01

    Reply is given to the comment by A. Wyttenbach and L. Tobler in J. Radioanal. Nucl. Chem., 247 (2001) 457 on the article by Y. Miyamoto et. al. published in J. Radioanal. Nucl. Chem. 243 (2000) 747 on 'Minor and trace element determination of food spices and pulses of different origins by NAA and PAA'. (N.T.)

  9. Trace elements in renal disease and hemodialysis

    International Nuclear Information System (INIS)

    Miura, Yoshinori; Nakai, Keiko; Suwabe, Akira; Sera, Koichiro

    2002-01-01

    A number of considerations suggest that trace element disturbances might occur in patients with renal disease and in hemodialysis (HD) patients. Using particle induced X-ray emission, we demonstrated the relations between serum concentration, urinary excretion of the trace elements and creatinine clearance (Ccr) in randomized 50 patients. To estimate the effects of HD, we also observed the changes of these elements in serum and dialysis fluids during HD. Urinary silicon excretion decreased, and serum silicon concentration increased as Ccr decreased, with significant correlation (r=0.702, p<0.001 and r=0.676, p<0.0001, respectively). We also observed the increase of serum silicon, and the decrease of silicon in dialysis fluids during HD. These results suggested that reduced renal function and also dialysis contributed to silicon accumulation. Although serum selenium decreased significantly according to Ccr decrease (r=0.452, p<0.01), we could detect no change in urinary selenium excretion and no transfer during HD. Serum bromine and urinary excretion of bromine did not correlate to Ccr. However we observed a bromine transfer from the serum to the dialysis fluid that contributed to the serum bromine decrease in HD patients

  10. Trace element patterns in lichens following uranium mine closures

    International Nuclear Information System (INIS)

    Fahselt, D.; Wu, T.W.; Mott, B.

    1995-01-01

    Instrumental neutron activation analysis was used to determine trace elements in Cladina mitis (Sandst). Hale ampersand Culb. along transects extending from uranium mines at Elliot Lake and Agnew Lake in central Ontario, Canada. Levels of 11 elements were reported and the presence of uranium (U) was confirmed, although U concentrations were much less than in Cladina rangiferina 10 years earlier. Among the elements identified in lichen thalli was Th, which occurred in higher concentrations than U. All trace elements, including the two radionuclides, were found in deteriorating thallus parts as well as living podetia, and five of these seem to have originated as airborne particulates from minesites. In spite of mine closures, levels of Th and U remained higher near sources of ore dust and there was little relationship between radionuclide concentrations in thallus and substrate. 24 refs., 4 figs., 3 tabs

  11. A back-arc setting for mafic rocks of the Honeysuckle Beds, southeastern N.S.W.: the use of trace and rare earth element abundances determined by INAA

    Energy Technology Data Exchange (ETDEWEB)

    Dadd, K A [University of Technology, Sydney, NSW (Australia)

    1994-12-31

    Major, trace and rare earth elements abundance in mafic rocks of the Honeysuckle Beds was determined by x-ray fluorescence and neutron activation analysis . A comparison with typical mid-ocean ridge basalt compositions reveals an enrichment in light rare earths elements (Ba, Rb, and Th) and depletion in Nb, Ta and Ti, consistent with modifications of the source by subduction-related fluids. 9 refs., 6 figs.

  12. A back-arc setting for mafic rocks of the Honeysuckle Beds, southeastern N.S.W.: the use of trace and rare earth element abundances determined by INAA

    Energy Technology Data Exchange (ETDEWEB)

    Dadd, K.A. [University of Technology, Sydney, NSW (Australia)

    1993-12-31

    Major, trace and rare earth elements abundance in mafic rocks of the Honeysuckle Beds was determined by x-ray fluorescence and neutron activation analysis . A comparison with typical mid-ocean ridge basalt compositions reveals an enrichment in light rare earths elements (Ba, Rb, and Th) and depletion in Nb, Ta and Ti, consistent with modifications of the source by subduction-related fluids. 9 refs., 6 figs.

  13. Multielement determination and speciation of major-to-trace elements in black tea leaves by ICP-AES and ICP-MS with the aid of size exclusion chromatography

    International Nuclear Information System (INIS)

    Matsuura, Hirotaka; Hokura, Akiko; Katsuki, Fumie; Itoh, Akihide; Haraguchi, Hiroki

    2001-01-01

    A multielement determination of major-to-trace elements in black tea leaves and their tea infusions was carried out by ICP-AES (inductively coupled plasma atomic emission spectrometry) and ICP-MS (inductively coupled plasma mass spectrometry). Tea infusions were prepared as usual tea beverage by brewing black tea leaves in boiling water for 5 min. About 40 elements in tea leaves and tea infusions could be determined over the wide concentration range in 8 orders of magnitude. The extraction efficiency of each element was estimated as the ratio of its concentration in tea infusions to that in tea leaves. From the experimental results for the extraction efficiencies, the elements in black tea leaves were classified into three characteristic groups: (i) highly-extractable elements (>55%): Na, K, Co, Ni, Rb, Cs and Tl, (ii) moderately-extractable elements (20-55%): Mg, Al, P, Mn and Zn, and (iii) poorly-extractable elements (<20%): Ca, Fe, Cu, Sr, Y, Zr, Mo, Sn, Ba and lanthanoid elements. Furthermore, speciation of major-to-trace elements in tea infusions was performed by using a combined system of size exclusion chromatography (SEC) and ICP-MS (or ICP-AES). As a result, many diverse elements were found to be present as complexes associated with large organic molecules in tea infusions. (author)

  14. Analytical evaluation of nebulizers for the introduction of acetic acid extracts aiming at the determination of trace elements by inductively coupled plasma mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Gois, Jefferson S. de; Maranhao, Tatiane de A. [Departamento de Quimica, Universidade Federal de Santa Catarina, 88040-970, Florianopolis, SC (Brazil); Oliveira, Fernando J.S. [Petroleo Brasileiro S.A., Gerencia de Meio Ambiente, Rio de Janeiro, RJ (Brazil); Frescura, Vera L.A.; Curtius, Adilson J. [Departamento de Quimica, Universidade Federal de Santa Catarina, 88040-970, Florianopolis, SC (Brazil); Borges, Daniel L.G., E-mail: daniel.borges@ufsc.br [Departamento de Quimica, Universidade Federal de Santa Catarina, 88040-970, Florianopolis, SC (Brazil)

    2012-11-15

    Most of the official procedures aiming at classification of solid waste toxicity take into account metal solubility and bioavailability by means of extraction experiments using acetic acid solutions. Hence, the aim of this work was to investigate and optimize conditions to suppress the effect of acetic acid on the determination of trace elements using inductively coupled plasma mass spectrometry. The performance of four nebulizers (cross-flow (CFN), ultrasonic (USN), Meinhard (MN) and MicroMist (MMN)) were compared as to their efficiency in minimizing spectral and non-spectral effects on the determination of Ag, As, Ba, Cd, Cr, Hg, Pb and Se, with the ultimate goal to analyze acetic acid extracts obtained from solid waste residues. Operating conditions (desolvation temperatures for USN, RF power and nebulizer gas flow rates) were optimized individually for each nebulizer and for all analytes maintained in 0.14 mol L{sup -1} HNO{sub 3} solutions and in solutions prepared with acetic acid and acetic acid + NaOH, adjusted to pH 2.88 and 4.93, respectively. Pronounced non-spectral interferences for {sup 75}As and {sup 82}Se were observed in the presence of acetic acid for CF and MN, although to a less extent also for MMN and USN. Signal increase for blank solutions measured at m/z 208 ({sup 208}Pb) for CFN and MN, 107 ({sup 107}Ag) for USN and MN coupled to a cyclonic chamber and, m/z 82 ({sup 82}Se) for USN was observed, indicating an increased risk of spectral interference upon an increase in the concentration of acetic acid. Signal increase at specific m/z ratios, however, was not significant when the MMN was used, with the exception of m/z 52 ({sup 52}Cr) in acetic acid solutions, arising from the formation of {sup 40}Ar{sup 12}C{sup +}. This same effect was noticed for all nebulizers, although at noticeably different intensities. A signal stability study was performed, demonstrating that variations in the analytical signal were within a 20% range for all analytes

  15. Mathematical considerations regarding the stability of the trace element systems by linear regressions

    International Nuclear Information System (INIS)

    Mihai, Maria; Popescu, I.V.

    2002-01-01

    In this paper we present a mathematical model that would describe the stability and instability conditions, respectively of the organs of human body assumed as a living cybernetic system with feedback. We tested the theoretical model on the following trace elements: Mn, Zn and As. The trace elements were determined from the nose-pharyngeal carcinoma. We utilise the linear approximation to describe the dependencies between the trace elements determined in the hair of the patient. We present the results graphically. (authors)

  16. Trace elements in ancient ceramics: Pt.4

    International Nuclear Information System (INIS)

    Li Huhou; Sun Yongjun; Zhang Xiangdong

    1987-01-01

    In the last period of Tong Dynasty, Jingdezhen began its production of ceramics. During the Song Dynasty, the ceramic industry greatly developed and produced fine white ware at Hutian. In the Yuan Dynastry, Hutian became the centre of production making the world famous blue and white wares. Here are reported results of analyses of ancient porcelians of Hutian in Jiangdezhen by reactor neutron activation analysis. The results show that the patterns of eight rare earth elements are apparently different for products in different periods, indicating that methods for producing ceramics or kinds of clay used were different. The contents of some other trace elements such as hafnium, tantalum, thorium and uranium show the same regularity in difference of composition also

  17. Report on the IAEA-CU-2006-06 proficiency test on the determination of major, minor and trace elements in ancient Chinese ceramic

    International Nuclear Information System (INIS)

    Shakhashiro, A.; Trinkl, A.; Toervenyi, A.; Zeiller, E.; Benesch, T.; Sansone, U.

    2006-10-01

    The report summarises the results of a proficiency test conducted under the IAEA co-ordinated research project (CRP) F.2.30.23, ''Applications of nuclear analytical techniques to investigate the authenticity of art objects''. The proficiency test was organized and conducted by the Reference Materials Group of the Chemistry Unit (Physics, Chemistry and Instrumentation Laboratory) of the IAEA's analytical laboratories located in Seibersdorf (Austria). The objective of the CRP is to explore new fields of application for nuclear analytical techniques in art and archaeology. It will help to foster collaboration between museum conservators and analytical researchers. The dissemination of information on applications of advanced analytical techniques to art objects will stimulate the use of these techniques in developing Member States and help in conservation and recovery of national heritage. Historical artefacts and art objects are traded world wide and represent a potential source for forgery and false labelling. The market is huge and a large part of the trade is going from developing countries to the developed world where strict regulations can only be applied if convenient methods for checking the authenticity were available. Portable XRF (X-ray fluorescence) instruments for rapid screening analysis and PGNAA (Prompt Gamma Neutron Activation Analysis) portable systems based on neutron sources for field work, as well as laboratory based techniques such as PIXE (Proton Induced X-ray Emission) and INAA (Instrumental Neutron Activation Analysis) have been applied non-destructively to investigate the provenience of archaeological objects and to determine different layers of precious paintings. The results of the CRP will be provided to member states for preservation of national heritage and secure legal enforcement. In the frame of the co-ordinated research project it was foreseen to conduct a proficiency test on the determination of major, minor and trace elements in an

  18. Trace element distribution in the rat cerebellum

    International Nuclear Information System (INIS)

    Kwiatek, W.M.; Long, G.J.; Pounds, J.G.; Reuhl, K.R.; Hanson, A.L.; Jones, K.W.

    1989-10-01

    Spatial distributions and concentrations of trace elements (TE) in the brain are important because TE perform catalytic structural functions in enzymes which regulate brain function and development. We have investigated the distributions of TE in rat cerebellum. Structures were sectioned and analyzed by the Synchrotron Radiation Induced X-ray Emission (SRIXE) method using the NSLS X-26 white-light microprobe facility. Advantages important for TE analysis of biological specimens with x-ray microscopy include short time of measurement, high brightness and flux, good spatial resolution, multielemental detection, good sensitivity, and non-destructive irradiation. Trace elements were measured in thin rat brain sections of 20-micrometers thickness. The analyses were performed on sample volumes as small as 0.2 nl with Minimum Detectable Limits (MDL) of 50 ppb wet weight for Fe, 100 ppb wet weight for Cu, and Zn, and 1 ppM wet weight for Pb. The distribution of TE in the molecular cell layer, granule cell layer and fiber tract of rat cerebella was investigated. Both point analyses and two-dimensional semi-quantitative mapping of the TE distribution in a section were used

  19. Trace elements in oil shale. Progress report, 1976--1979

    Energy Technology Data Exchange (ETDEWEB)

    Chappell, W.R.

    1979-01-01

    The overall objective of the program is to evaluate the environmental and health consequences of the release of toxic trace elements (As, B, F, Mo, Se) by shale oil production and use. Some of the particularly significant results are: The baseline geochemical survey shows that stable trace elements maps can be constructed for numerous elements and that the trends observed are related to geologic and climatic factors. Shale retorted by above-ground processes tends to be very homogeneous (both in space and in time) in trace element content. This implies that the number of analytical determinations required of processed shales is not large. Leachate studies show that significant amounts of B, F, And Mo are released from retorted shales and while B and Mo are rapidly flushed out, F is not. On the other hand, As, Se, and most other trace elements ae not present in significant quantities. Significant amounts of F and B are also found in leachates of raw shales. Very large concentrations of reduced sulfur species are found in leachates of processed shale. Upon oxidation a drastic lowering in pH is observed. Preliminary data indicates that this oxidation is catalyzed by bacteria. Very high levels of B and Mo are taken up in some plants growing on processed shale with and without soil cover. These amounts depend upon the process and various site specific characteristics. In general, the amounts taken up decrease with increasing soil cover. On the other hand, we have not observed significant uptake of As, Se, and F into plants. There is a tendency for some trace elements to associate with specific organic fractions, indicating that organic chelation or complexation may play an important role. In particular, most of the Cd, Se, and Cr in shale oil is associated with the organic fraction containing most of the nitrogen-containing compounds.

  20. Trace elements in the atmosphere over South Africa

    International Nuclear Information System (INIS)

    Wells, R.B.; Van As, D.

    1976-01-01

    Natural sources of trace elements in the atmosphere are suspended soil particles, the evaporation of sea spray and smoke from veld fires. In urban and industrialised areas the main sources are fossil-fuel power plants, metallurgical smelters, blast furnaces, incinerators, automobiles, fossil-fueled locomotives and open fires in the Black townships. Often a source can be recognised by the relative concentrations of particular trace elements. A monitoring programme was established in 1974 by the Air Pollution Research Group of the CSIR and the Isotope and Radiation Division of the Atomic Energy Board in order to study the levels of trace elements in urban areas such as Johannesburg, Cape Town, and Durban, to measure the effects of industrialisation on trace elements levels in developing areas such as Richards Bay and Saldanha Bay and also to determine baseline values in rural areas. Extremely sensitive analytical techniques, e.g. neutron activation and atomic absorption were used for the analyses of filter samples. Methods of sampling and analysis are discussed and the preliminary results of this programme are presented

  1. Bioaccumulation of trace elements by Avicennia marina

    Directory of Open Access Journals (Sweden)

    Kandasamy Kathiresan

    2014-11-01

    Full Text Available Objective: To analyze the concentrations of 12 micro-nutrients (Al, B, Cd, Co, Cr, Cu, Fe, Mg, Mn, Ni, Pb, and Zn in different plant parts of Avicennia marina and its rhizosphere soil of the south east coast of India. Methods: The samples were acid digested, then analyzed by using inductively coupled plasma system (ICP-Optical Emission Spectrophotometer. Results: Levels of metals were found in the decreasing order: Cd>Co>Ni>Pb>B >Cr>Zn>Mg>Mn>Cu>Fe>Al. The soil held more levels of metals than plant parts, but within the permissible limits of concentration. Bark and root accumulated higher levels of trace elements in a magnitude of 10-80 folds than other plant parts. The overall bioaccumulation factor in the sampling sites of Vellar, Pichavaram and Cuddalore was 2.88, 1.42 0.47 respectively. Essential elements accumulate high in mature mangroves forest while non-essential elements accumulate high in the industrially polluted mangroves. Conclusions: The ratio between essential and non-essential elements was found higher in young mangrove forest than that in mature mangrove forest and polluted mangrove areas. Thus, the ratio of accumulation can be used as an index of the growth and pollution status of mangroves.

  2. The potential of mid- and near-infrared diffuse reflectance spectroscopy for determining major- and trace-element concentrations in soils from a geochemical survey of North America

    Science.gov (United States)

    Reeves, J. B.; Smith, D.B.

    2009-01-01

    In 2004, soils were collected at 220 sites along two transects across the USA and Canada as a pilot study for a planned soil geochemical survey of North America (North American Soil Geochemical Landscapes Project). The objective of the current study was to examine the potential of diffuse reflectance (DR) Fourier Transform (FT) mid-infrared (mid-IR) and near-infrared (NIRS) spectroscopy to reduce the need for conventional analysis for the determination of major and trace elements in such continental-scale surveys. Soil samples (n = 720) were collected from two transects (east-west across the USA, and north-south from Manitoba, Canada to El Paso, Texas (USA), n = 453 and 267, respectively). The samples came from 19 USA states and the province of Manitoba in Canada. They represented 31 types of land use (e.g., national forest, rangeland, etc.), and 123 different land covers (e.g., soybeans, oak forest, etc.). The samples represented a combination of depth-based sampling (0-5 cm) and horizon-based sampling (O, A and C horizons) with 123 different depths identified. The set was very diverse with few samples similar in land use, land cover, etc. All samples were analyzed by conventional means for the near-total concentration of 49 analytes (Ctotal, Ccarbonate and Corganic, and 46 major and trace elements). Spectra were obtained using dried, ground samples using a Digilab FTS-7000 FT spectrometer in the mid- (4000-400 cm-1) and near-infrared (10,000-4000 cm-1) at 4 cm-1 resolution (64 co-added scans per spectrum) using a Pike AutoDIFF DR autosampler. Partial least squares calibrations were develop using: (1) all samples as a calibration set; (2) samples evenly divided into calibration and validation sets based on spectral diversity; and (3) samples divided to have matching analyte concentrations in calibration and validation sets. In general, results supported the conclusion that neither mid-IR nor NIRS would be particularly useful in reducing the need for conventional

  3. The use of INAA for the determination of trace elements, in particular cadmium, in plastics in relation to the enforcement of pollution standards

    International Nuclear Information System (INIS)

    Bode, P.

    1993-01-01

    Many plastic products have relatively short life cycles. Upon final destruction, inorganic additives used for pigmentation, as polymer stabilizer or as flame retarding agent are being released to the environment. In a rapidly increasing way governmental authorities are setting limits to the use of inorganic additives, in particular cadmium, in plastics. INAA has attractive characteristics which may make authorities decide to select it for the control programs in relation to the enforcement of pollution standards. An evaluation is made of the use of INAA for such analysis; analysis protocols, sensitivities, and observed levels of other trace elements are being discussed. (author) 2 refs.; 2 tabs

  4. The content of minerals and trace elements in meals

    International Nuclear Information System (INIS)

    Bognar, A.; Schelenz, R.; Gruenewald, T.; Frahm, H.; Heine, K.; Wiechen, A.; Bundesanstalt fuer Milchforschung, Kiel

    1981-07-01

    Within the frame work of the research programme 'School Feeding', 68 menu items of different producers were investigated for the content of the minerals calcium, chlorine, iron, potassium, magnesium, sodium and phosphorus, and for the trace elements antimony, barium, bromine, cesium, chromium, hafnium, iridium,cobalt, copper, manganese, mercury, rubidium, scandium, selenium, silver, strontium, tin and zinc. For the analytical determination of the elements, instrumental neutron activation analysis and X-ray fluorometry were applied. The studies showed that a calculation of the content of minerals and trace elements in meals on the basis of recipes and nutritive tables for raw foods is not justified, expect for sodium and phosphorus, because incorrect results can be obtained for the majority of meals. (orig./MG) [de

  5. Trace element load in cancer and normal lung tissue

    International Nuclear Information System (INIS)

    Kubala-Kukus, A.; Braziewicz, J.; Banas, D.; Majewska, U.; Gozdz, S.; Urbaniak, A.

    1999-01-01

    Samples of malignant and benign human lung tissues were analysed by two complementary methods, i.e., particle induced X-ray emission (PIXE) and total reflection X-ray fluorescence (TRXRF). The concentration of trace elements of P, S, K, Ca, Ti, Cr, Mn, Fe, Cu, Zn, Se, Sr, Hg and Pb was determined in squamous cancer of lung tissue from 65 people and in the benign lung tumour tissue from 5 people. Several elements shows enhancement in cancerous lung tissue of women in comparison to men, i.e., titanium show maximum enhancement by 48% followed by Cr (20%) and Mn (36%). At the same time trace element concentration of Sr and Pb are declaimed by 30% and 20% in women population. Physical basis of used analytical methods, experimental set-up and the procedure of sample preparation are described

  6. Nuclear analytical methods for trace element studies in calcified tissues

    International Nuclear Information System (INIS)

    Chaudhry, M.A.; Chaudhry, M.N.

    2001-01-01

    Full text: Various nuclear analytical methods have been developed and applied to determine the elemental composition of calcified tissues (teeth and bones). Fluorine was determined by prompt gamma activation analysis through the 19 F(p,ag) 16 O reaction. Carbon was measured by activation analysis with He-3 ions, and the technique of Proton-Induced X-ray Emission (PIXE) was applied to simultaneously determine Ca, P, and trace elements in well-documented teeth. Dental hard tissues, enamel, dentine, cement, and their junctions, as well as different parts of the same tissue, were examined separately. Furthermore, using a Proton Microprobe, we measured the surface distribution of F and other elements on and around carious lesions on the enamel. The depth profiles of F, and other elements, were also measured right up to the amelodentin junction

  7. Trace elements in groundwater used for water supply in Latvia

    Science.gov (United States)

    Retike, Inga; Kalvans, Andis; Babre, Alise; Kalvane, Gunta; Popovs, Konrads

    2014-05-01

    Latvia is rich with groundwater resources of various chemical composition and groundwater is the main drinking source. Groundwater quality can be easily affected by pollution or overexploitation, therefore drinking water quality is an issue of high importance. Here the first attempt is made to evaluate the vast data base of trace element concentrations in groundwater collected by Latvian Environment, Geology and Meteorology Centre. Data sources here range from National monitoring programs to groundwater resources prospecting and research projects. First available historical records are from early 1960, whose quality is impossible to test. More recent systematic research has been focused on the agricultural impact on groundwater quality (Levins and Gosk, 2007). This research was mainly limited to Quaternary aquifer. Monitoring of trace elements arsenic, cadmium and lead was included in National groundwater monitoring program of Latvia in 2008 and 2009, but due to lack of funding the monitoring was suspended until 2013. As a result there are no comprehensive baseline studies regarding the trace elements concentration in groundwater. The aim of this study is to determine natural major and trace element concentration in aquifers mainly used for water supply in Latvia and to compare the results with EU potable water standards. A new overview of artesian groundwater quality will be useful for national and regional planning documents. Initial few characteristic traits of trace element concentration have been identified. For example, elevated fluorine, strontium and lithium content can be mainly associated with gypsum dissolution, but the highest barium concentrations are found in groundwaters with low sulphate content. The groundwater composition data including trace element concentrations originating from heterogeneous sources will be processed and analyzed as a part of a newly developed geologic and hydrogeological data management and modeling system with working name

  8. Environmental aspects of coal trace elements

    International Nuclear Information System (INIS)

    Swaine, D.J.

    1992-01-01

    The increasing use of coal, especially for power production, means that more attention is being given to environmental aspects. Some matters, for example, acid mine drainage, acid deposition and the relevance of coal-derived carbon and nitrogen oxides to the greenhouse effect are still being investigated in order to find methods of mitigation. However, much less attention has been given to possible untoward effects from trace elements in coal during mining, preparation and use. Occasional emotional outbursts, based on insufficient evidence, focus attention on arsenic, lead, cadmium, mercury and uranium. The best way to counter such claims is to provide proper information as a basis for more informed judgments. The comments contained in this article are mostly based on work done at the Commonwealth Science and Industrial Research Organization (CSIRO)

  9. Preparation of hair and nail samples for trace element analysis

    International Nuclear Information System (INIS)

    Scoble, H.A.; Litman, R.

    1978-01-01

    The method of washing of human hair and nail samples is examined by neutron activation and γ-ray analysis. The amounts of Na, K, Br, Au, Zn, and La that are removed by successive washings determine the optimum number of washing for removing these trace elements as surface contaminants. A total solution contact time with the nails is 5 minutes, and leaching effcts are observed after 6 washings

  10. Development of analytical methods for the determination of trace elements in sediment with Neutron ActivAtion method (NAA) and Inductively Coupled Plasma Mass Spectrometry (ICP-MS)

    International Nuclear Information System (INIS)

    Nam, Sang Ho; Kim, Jae Jin; Chung, Yong Sam; Kim, Sun Ha

    2005-01-01

    The analytical methods for the determination of major elements (Al, Ca, K, Fe, Mg) in sediment have been investigated with ICP-MS. The analytical results of major elements with Cool ICP-MS were much better than those with normal ICP-MS. The analytical results were compared with those of NAA. NAA were a little superior to ICP-MS for the determination of major elements in sediment, and NAA is a non-destructive analytical method. The analytical methods for the determination of minor elements (Cr, Ce, U, Co, Pb, As, Se) in sediment have been also studied with ICP-MS. The analytical results by standard calibration with ICP-MS were not accurate due to matrix interferences. Thus, internal standard method was applied, then the analytical results for minor element with ICP-MS were greatly improved. The analytical results obtained by ICP-MS were compared with those obtained by NAA. It showed that the two analytical methods have great capabilities for the determination of minor elements in sediments

  11. Applying of Factor Analyses for Determination of Trace Elements Distribution in Water from River Vardar and Its Tributaries, Macedonia/Greece

    Science.gov (United States)

    Popov, Stanko Ilić; Stafilov, Trajče; Šajn, Robert; Tănăselia, Claudiu; Bačeva, Katerina

    2014-01-01

    A systematic study was carried out to investigate the distribution of fifty-six elements in the water samples from river Vardar (Republic of Macedonia and Greece) and its major tributaries. The samples were collected from 27 sampling sites. Analyses were performed by mass spectrometry with inductively coupled plasma (ICP-MS) and atomic emission spectrometry with inductively coupled plasma (ICP-AES). Cluster and R mode factor analysis (FA) was used to identify and characterise element associations and four associations of elements were determined by the method of multivariate statistics. Three factors represent the associations of elements that occur in the river water naturally while Factor 3 represents an anthropogenic association of the elements (Cd, Ga, In, Pb, Re, Tl, Cu, and Zn) introduced in the river waters from the waste waters from the mining and metallurgical activities in the country. PMID:24587756

  12. Applying of Factor Analyses for Determination of Trace Elements Distribution in Water from River Vardar and Its Tributaries, Macedonia/Greece

    Directory of Open Access Journals (Sweden)

    Stanko Ilić Popov

    2014-01-01

    Full Text Available A systematic study was carried out to investigate the distribution of fifty-six elements in the water samples from river Vardar (Republic of Macedonia and Greece and its major tributaries. The samples were collected from 27 sampling sites. Analyses were performed by mass spectrometry with inductively coupled plasma (ICP-MS and atomic emission spectrometry with inductively coupled plasma (ICP-AES. Cluster and R mode factor analysis (FA was used to identify and characterise element associations and four associations of elements were determined by the method of multivariate statistics. Three factors represent the associations of elements that occur in the river water naturally while Factor 3 represents an anthropogenic association of the elements (Cd, Ga, In, Pb, Re, Tl, Cu, and Zn introduced in the river waters from the waste waters from the mining and metallurgical activities in the country.

  13. Methodology for determination of trace elements in mineral phases of iron banded formation by LA-ICP-MS; Metodologia de determinacao de elementos-traco em fases minerais de formacoes ferriferas bandadas por LA-ICP-MS

    Energy Technology Data Exchange (ETDEWEB)

    Sousa, Denise V.M. de; Nalini Junior, Herminio A.; Sampaio, Geraldo M.S.; Abreu, Adriana T. de; Lana, Cristiano de C., E-mail: deniseversiane2@yahoo.com.br, E-mail: nalini@degeo.ufop.br, E-mail: geraldomssampaio@gmail.com, E-mail: adrianatropia@gmail.com, E-mail: cristianodeclana@gmail.com [Universidade Federal de Ouro Preto (DEGEO/UFOP), Ouro Preto, MG (Brazil). Departamento de Geologia

    2015-07-01

    The study of the chemical composition of mineral phases of iron formation (FF), especially of trace elements, is an important tool in the understanding of the genesis of these rocks and the contribution of the phases in the composition of whole rock. Low mass fraction of such elements in the mineral phases present in this rock type requires a suitable analytical procedure. The laser ablation technique coupled with ICP-MS (LA-ICP-MS) has been widely used for determination of trace elements in geological samples. Thus, the aim of this study is to develop calibration curves for determination of trace elements (Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) in mineral phases of banded iron formations by LA-ICP-MS. Several certified reference materials (CRM) were used for calibrate the equipment. The analytical conditions were checked by CRM NIST SRM 614. The results were satisfactory, since the curves showed good linearity coefficients, good accuracy and precision of results. (author)

  14. Trace elements levels in centenarian ‘dodgers’

    OpenAIRE

    Alis, Rafael; Santos-Lozano, Alejandro; Sanchís-Gomar, Fabián; Pareja Galeano, Helios; Fiuza Luces, María del Carmen; Garatachea, Nuria; Lucía Mulas, Alejandro; Emanuele, Enzo

    2016-01-01

    Trace element bioavailability can play a role in several metabolic and physiological pathways known to be altered during the aging process. We aimed to explore the association of trace elements with increased lifespan by analyzing the circulating levels of seven trace elements (Cr, Cu, Fe, Mn, Mo, Se and Zn) in a cohort of healthy centenarians or ‘dodgers’ (≥100 years, free of major age-related diseases) in comparison with sex-matched younger elderly controls. Centenarians showed significant ...

  15. Development of a certified reference material (NMIJ CRM 7531-a) for the determination of trace cadmium and other elements in brown rice flour.

    Science.gov (United States)

    Miyashita, Shin-ichi; Inagaki, Kazumi; Narukawa, Tomohiro; Zhu, Yanbei; Kuroiwa, Takayoshi; Hioki, Akiharu; Chiba, Koichi

    2012-01-01

    A certified reference material (CRM) for trace cadmium and other elements in brown rice flour was developed at the National Metrology Institute of Japan (NMIJ). The CRM was provided as a dry powder after drying and frozen pulverization of fresh brown rice obtained from a Japanese domestic market. Characterization of the property value for each element was carried out exclusively by NMIJ with at least two independent analytical methods, including inductively coupled plasma mass spectrometry (ICP-MS), ICP high-resolution mass spectrometry, isotope-dilution ICP-MS, ICP optical emission spectrometry, and graphite-furnace atomic-absorption spectrometry. Property values were provided for six elements (Mn, Fe, Cu, Zn, As, and Cd). The concentration range of the property values was from 0.280 mg kg(-1) of As to 31.8 mg kg(-1) of Zn. The combined relative standard uncertainties of the property values were estimated by considering the uncertainties of the homogeneity, characterization, difference among analytical methods, dry-mass correction factor, and calibration standard. The range of the relative combined standard uncertainties was from 1.1% of Zn to 1.6% of As.

  16. Determination of trace elements in coffee beans by XRF spectrometer equipped with polarization optics and its application to identification of their production area

    International Nuclear Information System (INIS)

    Akamine, Takao; Otaka, Akiko; Nakai, Izumi; Hokura, Akiko; Ito, Yuji

    2010-01-01

    The production area of coffee beans becomes a brand name, which gives reputations for the products, which is related to the price. This leads to room for mislabeling the products by unscrupulous market dealers. A rapid and easy method for the analysis of trace-element composition of coffee beans, which could be a good indicator of their production area, was studied in the present work. Coffee beans of 6 different regions (Brazil, Colombia, Vietnam, Indonesia, Tanzania, Guatemala) were analyzed by using a highly sensitive X-ray fluorescence spectrometer with three dimensional polarization optics. The experimental conditions were optimized so as to analyze 6 elements (Mn, Fe, Ni, Rb, Sr, Ba) in coffee beans, and linear calibration curves were obtained for the quantitative analysis of those elements. The analytical results were used in principal-component analysis to classify the coffee beans according to the geographical origin, which results in a successful characterization of the 6 production areas. It is found that roasted beans can be used with the same criterion as their green beans. Consequently, a rapid and easy way for the characterization of the geographic origin of coffee beans has been established in this study. (author)

  17. Trace elements in sera from patients with visceral leishmaniasis

    Energy Technology Data Exchange (ETDEWEB)

    Mukhopadhyay, R.; Bhattacharya, A. [Department of Zoology, Calcutta University, Calcutta (India); Chakraborty, A.; Sudarshan, M.; Jal, P.K.; Chintalapudi, S.N. [Inter University Consortium for DAE Facilities, Calcutta Centre 3/LB-8, Bidhan Nagar, Calcutta (India); Dutta, R.K. [Schonland Research Centre for Nuclear Sciences, University of Witwatersrand, Johannesburg (South Africa)

    2000-07-01

    Trace elements are known to have pivotal role in human health and disease. Present investigation employed PIXE analysis to probe into the elemental profile of patients suffering from visceral Leishmaniasis. Remarkable alternations were observed in concentration of elements like Cl, K, Ca, Mn, Fe, Cu, Zn. The pattern of enhancement of elemental concentration corresponds to the progression of the disease. Additionally, our present data reflect probable correlation between alteration in trace elemental status and other pathological syndromes associated with Leishmaniasis. The possibility of considering trace elements as a diagnostic marker for a better understanding of the disease is discussed. (author)

  18. Trace elements in sera from patients with visceral leishmaniasis

    International Nuclear Information System (INIS)

    Mukhopadhyay, R.; Bhattacharya, A.; Chakraborty, A.; Sudarshan, M.; Jal, P.K.; Chintalapudi, S.N.; Dutta, R.K.

    2000-01-01

    Trace elements are known to have pivotal role in human health and disease. Present investigation employed PIXE analysis to probe into the elemental profile of patients suffering from visceral Leishmaniasis. Remarkable alternations were observed in concentration of elements like Cl, K, Ca, Mn, Fe, Cu, Zn. The pattern of enhancement of elemental concentration corresponds to the progression of the disease. Additionally, our present data reflect probable correlation between alteration in trace elemental status and other pathological syndromes associated with Leishmaniasis. The possibility of considering trace elements as a diagnostic marker for a better understanding of the disease is discussed. (author)

  19. Determination of macro, essential trace elements, toxic heavy metal concentrations, crude oil extracts and ash composition from Saudi Arabian fruits and vegetables having medicinal values

    Directory of Open Access Journals (Sweden)

    Hana R. Alzahrani

    2017-11-01

    Full Text Available The concentrations of essential elements (Mg, Ca, Na, K, Fe, Zn, Se, Al, Ni, and Cu and toxic heavy metals (Pb, As, Cr, Cd, and Cr from Saudi Arabian fruits and vegetables were determined by inductively coupled plasma optical emission spectrophotometry (ICP/OES. Two types of butters, Caralluma munbayana and Caralluma hesperidum, Vigna (Vigna unguiculata, common fig (Ficus carica, Annona seeds (Annonaceae seeds, Annona fruits (Annonaceae fruits, Fennel (Foeniculum vulgare, and Fennel flowers (Nigella sativa were investigated, because they are used by indigenous groups as traditional medicines with Soxhlet-extraction and dry-ashing protocol. The estimated daily dietary element intake in food samples was further calculated in order to evaluate the element dietary intake and fruit and vegetable consumption pattern of the indigenes of Saudi Arabia. The crude oil and ash compositions varied widely, but suggested that most of the foods were good sources of oils and minerals. The figures-of-merit of the ICP-OES calibration curves were excellent with good linearity (R2 > 0.9921. The use of ICP-OES in this study allowed the accurate analysis and the detection of the elements at low levels. Essential elements (K, Ca, Na, and Mg had the highest concentrations while toxic heavy metals (As, Pb, and Cd had the lowest in the foods. Essential element pairs (Mg-Na, Mg-Ca, Fe-Al were highly correlated, suggesting that these foods are sources of multiple nutrients. Toxic element pairs (Pb-Cd, Pb-As, and Cd-As, however, were poorly correlated in the foods, suggesting that these elements do not have a common source in these foods. Average consumption of these foods should provide the recommended daily allowances of essential elements, but will not expose consumers to toxic heavy metals. The ICP-OES method was validated by determining method detection limits and percent recoveries of laboratory-fortified blanks, which were generally 90–100%.

  20. Baring the teeth. [Dental caries and the analysis of trace elements in dental tissues

    Energy Technology Data Exchange (ETDEWEB)

    Cleaton-Jones, P [University of the Witwatersrand, Johannesburg (South Africa). Dental Research Unit; Retief, H [Alabama Univ., Birmingham (USA); Turkstra, J [Fort Hare Univ. (South Africa). Dept. of Chemistry

    1979-07-01

    To determine whether trace elements other than fluorine play a role in the varying prevalences of dental caries in different South African population groups, neutron activation techniques have been devised to establish the concentrations of trace elements in tooth enamel and dentine.