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Sample records for determine present elements

  1. System to determine present elements in oily samples

    International Nuclear Information System (INIS)

    Mendoza G, Y.

    2004-11-01

    In the Chemistry Department of the National Institute of Nuclear Investigations of Mexico, dedicated to analyze samples of oleaginous material and of another origin, to determine the elements of the periodic table present in the samples, through the Neutron activation analysis technique (NAA). This technique has been developed to determine majority elements in any solid, aqueous, industrial and environmental sample, which consists basically on to irradiate a sample with neutrons coming from the TRIGA Mark III reactor and to carry out the analysis to obtain those gamma spectra that it emits, for finally to process the information, the quantification of the analysis it is carried out in a manual way, which requires to carry out a great quantity of calculations. The main objective of this project is the development of a software that allows to carry out the quantitative analysis of the NAA for the multielemental determination of samples in an automatic way. To fulfill the objective of this project it has been divided in four chapters: In the first chapter it is shortly presented the history on radioactivity and basic concepts that will allow us penetrate better to this work. In the second chapter the NAA is explained which is used in the sample analysis, the description of the process to be carried out, its are mentioned the characteristics of the used devices and an example of the process is illustrated. In the third chapter it is described the development of the algorithm and the selection of the programming language. The fourth chapter it is shown the structure of the system, the general form of operation, the execution of processes and the obtention of results. Later on the launched results are presented in the development of the present project. (Author)

  2. System to determine present elements in oily samples; Sistema para determinar elementos presentes en muestras oleosas

    Energy Technology Data Exchange (ETDEWEB)

    Mendoza G, Y

    2004-11-01

    In the Chemistry Department of the National Institute of Nuclear Investigations of Mexico, dedicated to analyze samples of oleaginous material and of another origin, to determine the elements of the periodic table present in the samples, through the Neutron activation analysis technique (NAA). This technique has been developed to determine majority elements in any solid, aqueous, industrial and environmental sample, which consists basically on to irradiate a sample with neutrons coming from the TRIGA Mark III reactor and to carry out the analysis to obtain those gamma spectra that it emits, for finally to process the information, the quantification of the analysis it is carried out in a manual way, which requires to carry out a great quantity of calculations. The main objective of this project is the development of a software that allows to carry out the quantitative analysis of the NAA for the multielemental determination of samples in an automatic way. To fulfill the objective of this project it has been divided in four chapters: In the first chapter it is shortly presented the history on radioactivity and basic concepts that will allow us penetrate better to this work. In the second chapter the NAA is explained which is used in the sample analysis, the description of the process to be carried out, its are mentioned the characteristics of the used devices and an example of the process is illustrated. In the third chapter it is described the development of the algorithm and the selection of the programming language. The fourth chapter it is shown the structure of the system, the general form of operation, the execution of processes and the obtention of results. Later on the launched results are presented in the development of the present project. (Author)

  3. Determination of some elements present in black pepper by thermal neutron activation analysis. [/sup 124/Sb-Be neutron source

    Energy Technology Data Exchange (ETDEWEB)

    Chacharkar, M P; Vaidya, M M; Ray, M N [Nagpur Univ. (India). Dept. of Chemistry

    1981-01-01

    An analysis for the determination of some elements present in black pepper was carried out using low level isotopic neutron source. Gamma-ray spectra of the irradiated samples showed only one peak at 0.85 MeV. The decay curves, on the other hand exhibited the presence of at least two radioactive nuclides of halflives 2.6 h and 15 h which correspond to the halflives of /sup 56/Mn and /sup 24/Na respectively. The amount of Mn present was also determined. The results are confirmed by other physicochemical methods. 6 refs.

  4. Determination of strontium in drinking water and consequences of radioactive elements present in drinking water for human health

    OpenAIRE

    Rajković Miloš B.; Stojanović Mirjana D.; Pantelić Gordana K.; Vuletić Vedrana V.

    2006-01-01

    In this paper the analysis of strontium and uranium content in drinking water has been done, indirectly, according to the scale which originates from drinking water in water-supply system of the city of Belgrade. Gamaspectrometric analysis showed the presence of free natural radionuclide in low activities. The activity of 90Sr in scale which is 0.72±0.11 Bq/kg was determined by radiochemical. Because of the small quantities of fur in the house heater this activity can be considered as irrelev...

  5. Determination of strontium in drinking water and consequences of radioactive elements present in drinking water for human health

    International Nuclear Information System (INIS)

    Rajkovic, M.B.; Stojanovic, M.D.; Pantelic, G.K.; Vuletic, V.V.

    2006-01-01

    In this paper the analysis of strontium and uranium content in drinking water has been done, indirectly, according to the scale which originates from drinking water in water-supply system of the city of Belgrade. Gamaspectrometric analysis showed the presence of free natural radionuclide in low activities. The activity of 90Sr in scale which is 0.72±0.11 Bq/kg was determined by radiochemical. Because of the small quantities of fur in the house heater this activity can be considered as irrelevant, but the accumulation of scale can have intensified influence. In this paper, the analysis of effects of the radioactive isotopes presence (first of all 238U and 235U) in drinking water on human health has been done

  6. The Transuranium Elements - Present Status: Nobel Lecture

    Science.gov (United States)

    Seaborg, G. T.

    1951-12-12

    The discovery of the transuranium elements and the work done on them up to the present time are reviewed. The properties of these elements, their relationship to other elements, their place in the periodic table, and the possibility of production and identification of other transuranium elements are discussed briefly.

  7. Transuranium elements: Past, present, and future

    International Nuclear Information System (INIS)

    Seaborg, G.T.

    1995-01-01

    In this illustrative Account the authors shall concentrate on four of these elements, chosen for their current interest or pivotal role. The story of plutonium is one of the most dramatic in the history of science, and today, plutonium is at the focus of an extraordinary dilemma. Mendelevium (element 101) has played a pivotal role in blazing the trail for the discovery of the heaviest elements on the basis of open-quotes one atom at a timeclose quotes production. Seaborgium (element 106) was recently named in my honor by the discoverers and may be the last element, at least for some time, for which it will be possible to determine many chemical properties. And element 110 represents recent evidence, after a lapse of 10 years, for the discovery of a chemical element. Recent (1994) recommendations of the IUPAC Commission on the Nomenclature of Inorganic Chemistry for the renaming of elements 104-108 have met with widespread rejection. The author is using the names proposed by the acknowledged discoverers (elements 106-109) or, in the case of the disputed elements 104 and 105, the most logical names. 21 refs., 5 figs

  8. 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)

  9. Present art of reactivity determination

    International Nuclear Information System (INIS)

    Kaneko, Yoshihiko; Nakano, Masafumi; Matsuura, Shojiro

    1977-01-01

    Experimental techniques for reactivity determination of a reactor have been one of the long standing subjects in reactor physics. Recently, such a requirement was proposed by the reactor designers and operators that the values of reactivity should be measured more accurately. This is because importance is emphasized for the role of reactivity to the performance of reactor safety, economics and operability. Motivated by the requirement, some remarkable progresses are being made for the improvement of the experimental techniques. Then, the present review summarizes the research activities on this subject, identifies several reactor physics problems to be overcome, and makes mention of the future targets. (auth.)

  10. Tips for better visual elements in posters and podium presentations.

    Science.gov (United States)

    Zerwic, J J; Grandfield, K; Kavanaugh, K; Berger, B; Graham, L; Mershon, M

    2010-08-01

    The ability to effectively communicate through posters and podium presentations using appropriate visual content and style is essential for health care educators. To offer suggestions for more effective visual elements of posters and podium presentations. We present the experiences of our multidisciplinary publishing group, whose combined experiences and collaboration have provided us with an understanding of what works and how to achieve success when working on presentations and posters. Many others would offer similar advice, as these guidelines are consistent with effective presentation. FINDINGS/SUGGESTIONS: Certain visual elements should be attended to in any visual presentation: consistency, alignment, contrast and repetition. Presentations should be consistent in font size and type, line spacing, alignment of graphics and text, and size of graphics. All elements should be aligned with at least one other element. Contrasting light background with dark text (and vice versa) helps an audience read the text more easily. Standardized formatting lets viewers know when they are looking at similar things (tables, headings, etc.). Using a minimal number of colors (four at most) helps the audience more easily read text. For podium presentations, have one slide for each minute allotted for speaking. The speaker is also a visual element; one should not allow the audience's view of either the presentation or presenter to be blocked. Making eye contact with the audience also keeps them visually engaged. Health care educators often share information through posters and podium presentations. These tips should help the visual elements of presentations be more effective.

  11. Serum Trace Element Presentation in Female Wistar Rats ...

    African Journals Online (AJOL)

    Serum Trace Element Presentation in Female Wistar Rats administered with Paracetamol & Paracetamol/Methionine. AA Iyanda, FAA Adeniyi. Abstract. A number of therapeutic agents are known to alter serum trace element levels with dangerous consequences. An earlier study had demonstrated significant alteration in the ...

  12. 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

  13. Separation and spectrophotometric determination of elements

    International Nuclear Information System (INIS)

    Marczenko, Z.

    1986-01-01

    This book is a useful text intended as a reference for the laboratory that is either involved in spectrophotometric analysis or requires separations prior to analysis by any method. It attempts to cover a diverse series of topics in fewer than 700 pages. Part I of the book covers general topics such as separation schemes (solvent extraction, precipitation, volatility, ion exchange), principles and instrumentation used for spectrophotometry, and color reagents in only 119 pages. Entire books have been written on each of those subjects. The author must therefore resort to extensive referencing to cover each subject adequately. Part II, Methods for Separation and Determination of Individual Elements, discusses all elements - both nonmetals and metals and major procedures for the separation and spectrophotometric determination of each element are adequately covered

  14. Determination of mutually interfering elements in activation analysis

    International Nuclear Information System (INIS)

    Figueiredo, A.M.G.

    1979-01-01

    The determination of the elements present in the groups scandium-zinc, mercury-selenium and arsenic-antimony-bromine represents a classical problem in thermal neutron activation analysis because the gamma-ray peaks of the radioisotopes produced from these elements by activation appear very close in the spectrum. A study is made of the possibility of simultaneous instrumental determination of these elements by means of the spectrum stripping technique, using a 400-channel analyser coupled to a Nal(Tl) detector and a 4096-channel analyser coupled to a Ge(Li) detector. Artificial mixtures of the interfering elements in varying proportions are prepared, so as to reproduce possible real samples, where the elements may be present at several concentrations. Radiochemical separation techniques for the cited elements are studied with the use of tracers. For the separation of scadium and zinc, the technique of extraction chromatography is applied. The separation of mercury and selenium is accomplished by means of ion exchange. The technique of coprecipitation is used to separate bromine from arsenic and antimony followed by ion exchange to isolate these two elements from each other. The precision and the accuracy of the results are discussed. (Author) [pt

  15. Determination of toxic elements in Malaysian foodstuffs

    International Nuclear Information System (INIS)

    Hamzah, Z.; Wood, A.K.H.; Mahmood, C.S.; Hamzah, S.

    1988-01-01

    This project is concentrating on the analysis of toxic elements content in seafoods including fishes, mussel, squid and prawn. Samples were collected from various places throughout Malay Peninsular. Samples were prepared according to RCA research protocol - nuclear techniques for toxic element in foodstuffs. Techniques used for elemental analysis were neutron activation analysis (instrumental and radiochemical) and anodic stripping voltametry. (author). 9 refs, 9 tabs

  16. Didactic interpretation of present conception of periodic table of elements

    International Nuclear Information System (INIS)

    Kysel, O; Juhasz, J.

    1999-01-01

    In this paper authors present modern didactic interpretation of periodic table of elements based on the electron structure of valent sphere of atoms which are classified into periods and groups. The accent is puttied on the nature of valent sphere and on the energy of electrons in this sphere (ionization potential) and their space distribution. These values are cardinal for character of chemical bonds in compounds and multiformity of structure of compounds. In this contribution new knowledge about electron structure of heavy atoms (relativistic effects of inner electrons on valent electrons) and properties of chemical compounds with unique using (high temperature superconductors, chemical substances for lasers and optoelectronic fibers and others). Using of uranium and plutonium in energetics is discussed

  17. 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

  18. Determination of isotopomers in pools of molecules with polyisotopic elements

    International Nuclear Information System (INIS)

    Zyakun, A.M.; Brenninkmeijer, C.A.M.

    2002-01-01

    Polyisotopic element atoms that are present in a molecule form a pool of isotopomer molecules. Mono- and polyisotopomers are distinguished depending on the quantity of atoms of polyisotopic elements. Methodical approaches have been considered for the quantitative determination of the isotope composition of an element included in mono- and polyisotopic molecules. A possibility of the equally probable (homogeneous) and non-equally probable (non-homogeneous) distribution of isotopes of a polyisotopic element, the atoms of which have different positions in the molecule of polyisotopomer, has been shown. Factors disturbing the homogeneous distribution of isotopes of the element in the polyisotopomer pool have been revealed. When a polyisotopomer is involved in a mass-dependent process or reaction, the homogeneity of isotope distribution of the element is disturbed both in the residual and newly formed pools of polyisotopomer. By the example of CO 2 (polyisotopomer by oxygen) it has been shown that one can judge of the history of the analyzed pool formation by distribution of oxygen isotopes within this pool. The isotope content in the oxygen sites of polyisotopomer is a diagnostic feature of CO 2 involvement in the efflux from a reservoir or influx to the analyzed reservoir from an external source. (author)

  19. Determination of ash-forming elements in lignite coal

    International Nuclear Information System (INIS)

    Wischnewski, C.; Werner, G.; Vogt, J.; Just, G.

    1990-01-01

    The most important methods are discussed suitable for the determination of ash-forming elements in coal. In this connection questions of the concentrations of elements in lignites, of the sample preparation, and of the selection of methods for the determination of ash-forming elements are addressed. Advantages and disadvantages of different analysis techniques are shown using concrete examples. (author)

  20. Determination of the hydrogen content of fuel elements

    International Nuclear Information System (INIS)

    Soare, M.; Petriu, F.; Toma, V.

    1995-01-01

    A new method and apparatus are reported for determination of the total hydrogen content by measurements on as-manufactured fuel elements, heated at prescribed temperature values between 200 degrees C and 600 degrees C. The method is based on the catalytic oxidation of the organic compounds and transformation of the hydrogen in the equivalent water quantity which is analysed by a special infrared detector. Different types of measurements for determination of the hydrogen content from graphite coating, UO 2 pellets and filling gas are presented. Also, experimental observation regarding water release and graphite thermal decomposition kinetic are discussed. (author)

  1. Process to determine light elements content of steel and alloys

    Energy Technology Data Exchange (ETDEWEB)

    Quintella, Cristina M.A.L.T.M.H.; Castro, Martha T.P.O. [Universidade Federal da Bahia (IQ/UFBA), Salvador, BA (Brazil). Inst. de Quimica. LabLaser; Mac-Culloch, Joao N.L.M. [PETROBRAS, Rio de Janeiro, RJ (Brazil)

    2009-07-01

    The present work reports a process to determine qualitatively and quantitatively elements of molar mass inferior to 23 within materials, by X rays spectra associated with multivariate data analysis, or chemometric analysis. The spectra is acquired between 5 keV and 22 keV when the materials are exposed to X radiation. Here is reported the direct determination of carbon content in steel and metallic alloys. The process is more effective when using spectral regions which are not usually used. From the analysis of these spectral regions which were not considered before, it was possible to detect light elements with molar mass lower than 23, which have low capacity of absorbing and emitting radiation, but have high capacity of scattering radiation. The process here reported has the advantage that X-Ray spectra obtained are calibrated multivariately, showing high potential for development in order to be used in a portable field equipment. (author)

  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. Determining fissile content of nuclear fuel elements

    International Nuclear Information System (INIS)

    Arya, S.P.; Grossman, L.N.; Schoenig, F.C.

    1980-01-01

    This invention relates to the determination of the fissile fuel content of fuel for nuclear reactors. A nondestructive method is described for determining rapidly, accurately and simultaneously the fissile content, enrichment and location of fuel material which may also contain amounts of burnable poison, by detecting the γ-rays emitted from the fuel material due to natural radioactive decay. (U.K.)

  4. Present status and further objectives of SNR fuel element development

    International Nuclear Information System (INIS)

    Karsten, G.

    Within the scope of the fuel element development program for the fast breeder reactor SNR 300, 500 fuel pins have been irradiated since 1964, 250 of them in fast flux. Results indicate that the maximum nominal target burnup of 90.000 MWd/t of the SNR 300 Mk Ia possibly can be reached. The main problems, which arise from clad swelling and internal corrosion, can be met by special pretreatments of the austenitic stainless steel 1.4970 and a fuel stoichiometry of 1.97. Beyond this target burnup either material property improvements have to be made or burnup reductions have to be accepted. The remaining questions can be answered by the use of the SNR 300 as a test reactor. A further target is the development of a carbide fuel element, which should be very effective in a high power breeder reactor because of its low fissile inventory and high breeding gain. This development program will also be finalized in the SNR 300. (U.S.)

  5. Homology among tet determinants in conjugative elements of streptococci

    Energy Technology Data Exchange (ETDEWEB)

    Smith, M.D.; Hazum, S.; Guild, W.R.

    1981-10-01

    A mutation to tetracycline sensitivity in a resistant strain of Streptococcus pneumoniae was shown by several criteria to be due to a point mutation in the conjugative o(cat-tet) element found in the chromosomes of strains derived from BM6001, a clinical strain resistant to tetracycline and chloramphenicol. Strains carrying the mutation were transformed back to tetracycline resistance with the high efficiency of a point marker by donor deoxyribonucleic acids from its ancestral strain and from nine other clinical isolates of pneumococcus and by deoxyribonucleic acids from Group D Streptococcus faecalis and Group B Streptococcus agalactiae strains that also carry conjugative tet elements in their chromosomes. It was not transformed to resistance by tet plasmid deoxyribonucleic acids from either gram-negative or gram-positive species, except for one that carried transposon TN916, the conjugative tet element present in the chromosomes of some S. faecalis strains. The results showed that the tet determinants in conjugative elements of several streptococcal species share a high degree of deoxyribonucleic acid sequence homology and suggested that they differ from other tet genes.

  6. Presentation and qualification of criticality calculation in fuel element storage

    International Nuclear Information System (INIS)

    Ermumcu, G.; Gonnord, J.; Monnier, A.; Nimal, J.C.

    Faced with the growing size of criticality calculation requests a fast and slightly conservative method has been perfected for evaluating the effective multiplication constant of sites containing PWR type elements. This method is based on the use of the DOT 3.5 code which requires a bidimensional modelisation of the geometry of the problem and the placing into groups of the macroscopic cross sections of the various materials. This preliminary work is effected by various APOLLO calculations. This diagram is qualified by comparison with the results obtained by the Monte Carlo TRIPOLI code. Comparing the values obtained by MORET and APOLLO-DOT for the criticality of transport flask end in good agreement. For the parametric studies, a large number of calculations can be necessary, and analytical methods cost little for simple geometries. This diagram can be used for studying small transport flasks but it is particularly advantageous for storages [fr

  7. [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.

  8. Determination of toxic and essential elements in seafood

    International Nuclear Information System (INIS)

    Surtipanti, S.; Suwirma, S.; Yumiarti, S.; Yune Mellawati, T.

    1990-01-01

    Indonesia has only a list of the maximum permissible concentration of toxic elements in water stated in a national legislation. Therefore, it is important to study the toxic elements content in fish and shellfish, because these marine organisms are good biological indicators. The interesting elements to be analyzed are toxic elements, i.e. As, Cd, Cr, Hg, Pb, Sb and Se, and essential elements, i.e., Zn and Cu. As, Cr, Hg, Sb, Se and Zn can be determined by Neutron Activation Analysis (NAA), while Cd, Cu and Pb by Atomic Absorption Spectrometry (AAS). The determination of such elements in foodstuff i.e. rice, corn, green pea, wheat, vegetables, fruits, tea and coffee have been done previously. The major purpose of this work is to know whether the concentration of toxic elements in marine organisms is approaching or exceeding the maximum permissible concentration as stated by International legislation. 7 refs, 5 tabs

  9. Determination of positions of optical elements of the human eye

    International Nuclear Information System (INIS)

    Galetskii, S O; Cherezova, T Yu

    2009-01-01

    An original method for noninvasive determining the positions of elements of intraocular optics is proposed. The analytic dependence of the measurement error on the optical-scheme parameters and the restriction in distance from the element being measured are determined within the framework of the method proposed. It is shown that the method can be efficiently used for determining the position of elements in the classical Gullstrand eye model and personalised eye models. The positions of six optical surfaces of the Gullstrand eye model and four optical surfaces of the personalised eye model can be determined with an error of less than 0.25 mm. (human eye optics)

  10. Multi-element determination of soil solution by INAA

    International Nuclear Information System (INIS)

    Qian Qinfang; Wu Shuiqing; Tian Jibing

    1992-01-01

    One of the factors influencing crop growth is the effective elemental contents, especially trace elements, under the circumstances of the same concentrations of N, P and K in soil. In order to obtain the data of effective elemental contents in soil, a novel method was introduced. In this method, soil solution was extracted by a squeezer. The concentrations of elements in soil solution were determined by INAA. Study on the compositions and the contents of elements in soil solution will provide information on making a suitable soil environment for plant growth and on rational and economical manuring

  11. ECONOMIC EFFICIENCY - DETERMINED ELEMENT IN INVESTMENT DECISION

    Directory of Open Access Journals (Sweden)

    Claudia MUNGIU-PUPAZAN

    2010-03-01

    Full Text Available Economic activity of a country are conducted by industry, under branches and production sectors, each with special characteristics and conditions of work, which, of course, put their imprint on the organization manner of the production process By an analysis of the concept of economic efficiency of investment is found that this is an amount of qualitative factors, which gives the latter a complex character, aimed to improving activity in the area where are taking place to the putting into service of such investment, which can be modernization, bringing new equipments, reconstruction and development. Study the economic efficiency of investment involves, as a base, an analysis of causal factors that determine the decision in the afferent medium of risk. Corresponding to peculiarities of the production process, it requires a proper methodology of assessment the economic efficiency of investment, with specification to maintain the general principles for calculating the economic efficiency indicators and specific indicators come only to complete the picture of indicators of general, basic and supplementary already calculated in order to provide additional clues, afferent to branch, under-branch or sector of activity.

  12. 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.)

  13. Determination of substraces of alpha emitter elements in water

    International Nuclear Information System (INIS)

    Gascon, J.L.

    1990-01-01

    To determine alpha emitter elements in water by alpha spectrometry, it is necessary to use large volumes of samples, concentration techniq-ues and to separate the elements of interest. In this report a study is presented about two concentration techniques and the process of analysis. Firstly, the stages of concentration method by iron hydroxide coprecipitation were studied in order to improve the results. The combination of liquid-liquid extraction and ion exchange techniques was the best way. Secondly, the technique by adsorption on manganese dioxide was studied. To apply this technique it was necessary to develop analysis methods to separate uranium, thorium, plutonium, americium and radium. These methods were designed combining several techniques of separation: liquid-liquid extraction, liquid-solid extraction, ionic exchange and coprecipitation. After the analysis methods were developped the adsorption on manganese dioxide with artificial samples was studied in the laboratory. Finally, the method of adsorption on manganese dioxide was studied to determine uranium, thorium and radium in the drinking water of Madrid. (Author)

  14. Enzymatic determination of rare earth elements using pyrophosphatases

    International Nuclear Information System (INIS)

    Shekhovtsova, T.N.; Pirogova, S.V.; Fedorova, O.M.; Dolmanova, I.F.; Bajkov, A.A.

    1993-01-01

    A highly sensitive(determination limit 8x10 -6 -4x10 -4 μ g/m) and selective enzymatic method for determination of rare earth elements has been developed. The method is based on inhibition action of rare earths on the catalytic activity of pyrophosphates isolated from bakery geast and E.Coli. The mechanism of the rare earth element action, corresponding to competitive inhibition, has been established

  15. Enzymatic determination of rare earth elements by use of pyrophosphotases

    International Nuclear Information System (INIS)

    Shekhovtseva, T.N.; Pirogova, S.V.; Fedorova, O.M.; Dolmanova, I.F.; Bajkov, A.A.

    1993-01-01

    A highly sensitive (determination limit 8 x 10 -6 - 4 x 10 -4 μg/ml) and selective enzymatic method for determination of rare earth elements has been developed. The method is based on inhibition action of rare earths on the catalytic activity of pyrophosphates isolated from bakery geast and E. Coli. The mechanism of the rare earth element action, corresponding to competitive inhibition, has been established

  16. 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

  17. 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)

  18. Determination of essential elements in formulas commercialized at the Sao Paulo state, Brazil

    International Nuclear Information System (INIS)

    Campos, Vinicius Dias; Vallinoto, Priscila; Maihara, Vera Akiko

    2011-01-01

    This paper intends to determine the concentration of elements, presents in the infant formulas, by using the Neutron Activation Analysis for verification if the quantity is not exceeding the toxicity limit, and if the concentration of each element is correct as presented on the label of each packaging

  19. Determination of rare earth elements in biomonitors by neutron activation

    International Nuclear Information System (INIS)

    Figueiredo, Ana M.G.; Saiki, Mitiko; Ticianelli, R.B.; Domingos, M.; Alves, E.S.; Marcelli, M.P.

    2000-01-01

    The rare earth elements (REE) are becoming more and more important from the technological point of view, due to their increasing use in modern industry. Due to this fact, environmental contamination by REE may become significant, and little information are still available about biological effects of REE in plants, animals and human beings. The use of biomonitors to control environmental pollution has been an ecological and economical alternative in Europe and United Sates, to minimize the high costs of conventional equipment s. In the present paper, neutron activation analysis was employed to determine La, Ce, Nd, Sm, Eu, Tb, Yb and Lu in the lichen Canoparmelia texana and in Tillandsia usneoides, species that have been widely used as monitors of atmospheric pollution. The results showed an accumulation of REE in the biomonitors, indicating good possibilities of their utilization in the study of environmental contamination by REE. (author)

  20. 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

  1. Determination of the Light Element Fraction in MSL APXS Spectra

    Science.gov (United States)

    Perrett, G. M.; Pradler, I.; Campbell, J. L.; Gellert, R.; Leshin, L. A.; Schmidt, M. E.; Team, M.

    2013-12-01

    Additional light invisible components (ALICs), measured using the alpha particle X-ray spectrometer (APXS), represent all light elements (e.g. CO3, OH, H2O) present in a sample below Na, excluding bound oxygen. The method for quantifying ALICs was originally developed for the Mars Exploration Rover (MER) APXS (Mallet et al, 2006; Campbell et al, 2008). This method has been applied to data collected by the Mars Science Laboratory (MSL) APXS up to sol 269 using a new terrestrial calibration. ALICs are investigated using the intensity ratio of Pu L-alpha Compton and Rayleigh scatter peaks (C/R). Peak areas of the scattered X-rays are determined by the GUAPX fitting program. This experimental C/R is compared to a Monte Carlo simulated C/R. The ratio of simulated and experimental C/R values is called the K-value. ALIC concentrations are calculated by comparing the K-value to the fraction of all invisibles present; the invisible fraction is produced from the spectrum fit by GUAPX. This method is applied to MSL spectra with long integration duration (greater than 3 hours) and with energy resolution less than 180 eV at 5.9 keV. These overnight spectra encompass a variety of geologic materials examined by the Curiosity Rover, including volcanic and sedimentary lithologies. Transfer of the K-value calibration produced in the lab to the flight APXS has been completed and temperature, geometry and spectrum duration effects have been thoroughly examined. A typical limit of detection of ALICs is around 5 wt% with uncertainties of approximately 5 wt%. Accurate elemental concentrations are required as input to the Monte Carlo program (Mallet et al, 2006; Lee, 2010). Elemental concentrations are obtained from the GUAPX code using the same long duration, good resolution spectra used for determining the experimental C/R ratios (Campbell et al. 2012). Special attention was given to the assessment of Rb, Sr, and Y as these element peaks overlap the scatter peaks. Mineral effects

  2. 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)

  3. Determination of plutoniumn and transplutonium elements in the environment

    International Nuclear Information System (INIS)

    Willemot, J.M.; Verry, M.; Jeanmaire, L.

    1988-01-01

    Environmental samples made of many different stable elements and natural emitting radionuclides must undergo chemical analysis allowing to prepare quality sources. Plutonium and americium sources with a good resolution can be obtained from environmental samples by successive operations of co-precipitation ion-exchange separation and solvent extraction. Spectral analysis is then simple and consequently plutonium and transplutonium elements are determined easily in such samples. 15 refs [fr

  4. Determining reactor fuel elements broken by Cerenkov counting

    International Nuclear Information System (INIS)

    Guo Juhao; Dong Shiyuan; Feng Yuying

    1996-01-01

    The basis and method of determining fuel elements broken in a reactor by Cerenkov counting measured with liquid scintillation spectrometer are introduced. The radioactive characteristic of the radiation nuclides generating Cherenkov radiation in the primary water of 200 MW nuclear district heating reactor is analyzed. The activity of the activation products in the primary water and the fission products in the fuel elements are calculated. A feasibility of Cerenkov counting measure was analyzed. This method is simple and quick

  5. Determination of elemental concentrations in environmental plant samples by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Datta, J.; Chowdhury, D.P.; Verma, R.; Reddy, A.V.R.

    2012-01-01

    The intake of leafy vegetables in daily diet is very important to meet our nutritional needs. Vegetables provide the essential elements which are necessary and recommended for human growth. However, due to rapid industrialization and urbanization our environment becomes polluted and this affects the normal growth of agricultural products and composition of environmental species. The elemental concentrations present in the environmental samples are good indicators to assess the toxicological levels due to pollution affects. In the present work we have analysed several vegetable plant samples by instrumental neutron activation analysis to determine the elemental concentrations at major, minor and trace levels. The leafy vegetables like spinach, red leafy vegetable, pui, gourd leaf, lettuce and katoua were chosen as these are extensively consumed by local people in eastern part of India. We have determined 15 elements in the above mentioned vegetable samples and some of these are essential elements and some are toxic elements. It was found that Na and K were present as major elements, Fe and Zn as minor elements and As, Ce, Cr, Co, La, Mo, Rb, Sc, Sm, Sr as trace elements. The concentration level of Cr was found to be higher than that of recommended value certified by WHO and National environment quality control for human consumption. The validation of our analytical results have been performed by the Z-score tests through the determination of concentrations of the elements of interest in certified reference materials. (author)

  6. 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

  7. 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.

  8. Determining e-Portfolio Elements in Learning Process Using Fuzzy Delphi Analysis

    Science.gov (United States)

    Mohamad, Syamsul Nor Azlan; Embi, Mohamad Amin; Nordin, Norazah

    2015-01-01

    The present article introduces the Fuzzy Delphi method results obtained in the study on determining e-Portfolio elements in learning process for art and design context. This method bases on qualified experts that assure the validity of the collected information. In particular, the confirmation of elements is based on experts' opinion and…

  9. 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

  10. 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.

  11. DETERMINATION OF MULTI ELEMENT LEVELS IN LEAVES AND ...

    African Journals Online (AJOL)

    Preferred Customer

    ICP-OES (Spectro Analytical Instruments, Kleve, Germany) was used for the determination of elements. ... Samples. In this study, 18 different herbal tea samples (leaves and flowers) that are traditionally used for medical ... analysis of CRM were all within the 95% reliability limit. The results ..... reasons for serious health risks.

  12. 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

  13. 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 ...

  14. On electrochemical sensor for determining elemental iodine in gas media

    International Nuclear Information System (INIS)

    Goffman, V.G.; Shajmerdinov, B.U.; Kotelkin, I.M.; Mikhajlova, A.M.; Dobrovol'skij, Yu.A.

    1993-01-01

    The possibility to use solid electrolyte cells of Ag, AgI/AgI/Au as sensors for determining concentration of element iodine in gaseous media was studied. Independent character of sensor parameters on oxygen content and radiation burden at different humidity was ascertained

  15. An electrochemical sensor for determining elemental iodine in gas media

    Energy Technology Data Exchange (ETDEWEB)

    Goffman, V.G.; Shaimerdinov, B.U.; Kotelkin, I.M. [Institute of New Chemical Problems, Moscow (Russian Federation)] [and others

    1993-12-01

    The possibility of using solid-electrolyte Ag, AgI/AgI/Au cells as sensors for determining the concentration of elemental iodine in gas media is investigated. It is established that the sensor parameters are independent of oxygen content and radiation dose at different relative humidities.

  16. Technique for mass-spectrometric determination of moisture content in fuel elements and fuel element claddings

    International Nuclear Information System (INIS)

    Kurillovich, A.N.; Pimonov, Yu.I.; Biryukov, A.S.

    1988-01-01

    A technique for mass-spectroimetric determination of moisture content in fuel elements and fuek claddings in the 2x10 -4 -1.5x10 -2 g range is developed. The relative standard deviation is 0.13. A character of moisture extraction from oxide uranium fuels in the 20-700 deg C temperature range is studied. Approximately 80% of moisture is extracted from the fuels at 300 deg C. The moisture content in fuel elements with granular uranium oxide fuels is measured. Dependence of fuel element moisture content on conditions of hot vacuum drying is shown. The technique permits to optimize the fuel element fabrication process to decrease the moisture content in them. 4 refs.; 3 figs.; 2 tabs

  17. Atomic absorption spectrometric determination of mineral elements in mammalian bones

    International Nuclear Information System (INIS)

    Udoh, Anthony P.

    2000-01-01

    The phosphorus content of the major bones of male and female selected mammals was determined using the yellow vanadomolybdate colorimetric method. For each animal, the bone with the highest phosphorus content was used as pilot sample. Varying concentrations of strontium were added to solutions of the ashed pilot samples to minimize phosphorus interference in the determination of calcium and magnesium using flame atomic absorption spectrophotometry operated on the air-acetylene mode. At least 6,000 ppm (0.6%) of strontium was required to give optimum results for calcium. The amount of magnesium obtained from the analysis was not affected by the addition of strontium. With the incorporation of strontium in the sample solution, all elements of interest can be determined in the same sample solution. Based on this, a procedure is proposed for the determination of calcium and other elements in bones. Average recoveries of spiked calcium and magnesium were 97.85% and 98.16%, respectively at the 95% confidence level. The coefficients of variation obtained for replicate determinations using one of the samples were 0.00% for calcium, lead and sodium, 2.93% for magnesium, 3.27% for iron and 3.92% for zinc at the concentration levels found in that sample. Results from the proposed procedure compared well with those from classical chemical methods at the 95% confidence level. It is evident that calcium phosphorus, magnesium and sodium which are the most abundant elements in the bones are distributed in varying amounts both in the different types of bones and different animal species, although the general trend is Ca > P > Na > Mg for each bone considered. The calcium - phosphorus ratio is generally 3:1. The work set out to propose an atomic absorption spectrometric method for the multi-element analysis of mammalian bones with a single sample preparation and to study the distribution pattern of these elements in the bones. (Author)

  18. Analysis of elements present in beers and brewing waters by neutron activation analysis

    International Nuclear Information System (INIS)

    Krausova, Ivana; Kucera, Jan; Dostalek, Pavel; Potesil, Vaclav

    2011-01-01

    Neutron activation analysis (NAA) was used for determination of Si, Na, K, Ca, Sc, V, Cr, Mn, Fe, Co, Zn, Rb, Cs, and La in Czech beers and brewing waters. The Si concentration in beer determined by the reaction 29 Si(n,p) 29 Al with fast neutrons confirmed that beer is an important Si source in human diet. Determination of other trace elements by NAA with the whole spectrum of reactor neutrons aimed at the feasibility of identification of Gambrinus beers brewed in various breweries. The elements Ca and V appeared to be the best candidates for this purpose. The concentrations of elements determined by NAA were also compared with the recommended daily element intake for humans. The accuracy of the method was proved by analysis of reference materials, specifically NIST SRM 2704 Buffalo River Sediment, NIST SRM 1633b Coal Fly Ash, and NIST SRM 1515 Apple Leaves. (author)

  19. Accurate determination of light elements by charged particle activation analysis

    International Nuclear Information System (INIS)

    Shikano, K.; Shigematsu, T.

    1989-01-01

    To develop accurate determination of light elements by CPAA, accurate and practical standardization methods and uniform chemical etching are studied based on determination of carbon in gallium arsenide using the 12 C(d,n) 13 N reaction and the following results are obtained: (1)Average stopping power method with thick target yield is useful as an accurate and practical standardization method. (2)Front surface of sample has to be etched for accurate estimate of incident energy. (3)CPAA is utilized for calibration of light element analysis by physical method. (4)Calibration factor of carbon analysis in gallium arsenide using the IR method is determined to be (9.2±0.3) x 10 15 cm -1 . (author)

  20. Determination of elements in blood of golden hamster by NAA

    International Nuclear Information System (INIS)

    Aguiar, Rodrigo Oliveira de

    2009-01-01

    In the present study Neutron Activation Analysis technique has been used to determine, simultaneously, some element concentrations of clinical relevance in whole blood samples of golden hamster. The normal range for Br, Ca, Cl K, Mg, Na and S considering 2 σ (Two Standard deviations) was 0.011 0.047 gL -1 (Br); 0.11 0.35 gL -1 (Ca); 2.11 3.75 gL -1 (Cl); 1.35 2.79 gL -1 (K), 0.026 0.090 gL -1 (Mg), 1.03 2.51 gL -1 (Na) e 0.97 2.01 gL -1 (S). The knowledge of these limits became possible to perform clinical investigation in this animal model using whole blood. The comparison with the results from human being whole blood estimation (Hamster and human) became possible to check the similarities or physiologic differences, an important data for animal experimentation. (author)

  1. 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

  2. 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

  3. 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)

  4. 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.

  5. Present status of research activities conducted by research group for heavy elements microbiology in JAERI

    International Nuclear Information System (INIS)

    Ohnuki, Toshihiko; Ozaki, Takuo; Yoshida, Takahiro

    2004-01-01

    It has been recognized that microbial transformations of radionuclides and toxic metals could be significant in the environment, but there is a paucity of information on the mechanisms of biotransformation of radionuclides by the microorganisms. An understanding at the fundamental level the mechanisms of mobilization, immobilization and bioavailability of radioactive elements in particular the actinides is important from the standpoint of mobility of actinides in the environment, disposal of radioactive wastes in deep geological formation, remediation of contaminated soils and materials, and development of strategies for the long-term stewardship of the contaminated sites. The microbiology research group in Japan Atomic Energy Research Institute (JAERI) is conducting basic scientific research on microbial interactions with actinides. Fundamental research on microbial transformations of actinides include elucidation of the mechanisms of dissolution and precipitation of various chemical forms such as ionic, oxides, organic and inorganic complexes of actinides by aerobic or anaerobic microorganisms under relevant microbial process conditions. State-of-the-art analytical techniques are used to determine the interaction of actinides with microorganisms at the molecular level to understand the structure function relationship. These techniques include time-resolved laser fluorescence spectroscopy (TRLFS) to determine the coordination number, oxidation states and the nearest neighbor by X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) at the Synchrotron Light Source, identification of functional groups by nuclear magnetic resonance (NMR), determination of chemical forms by transmission electron microscopy (TEM), and genomic (DNA) manipulation by molecular techniques. We here report the present status of our research activities on accumulation of lanthanides(III) by microorganisms, application of micro-particle induced X

  6. Determination of uranium, plutonium and transplutonium elements in urine

    International Nuclear Information System (INIS)

    Zablotskaya, I.D.; Vorob'ev, G.V.; Golutvina, M.M.

    1983-01-01

    An extraction-coprecipitation method is proposed for determining enriched U, Pu and transplutonium elements (Am, Cm, Cf) in urine of people having contact with these substances. The nuclides were extracted from HDEHP sulfuri.c acid solutions with a subsequent reextraction by ammonium carbonate and HCl. The reliability of the developed method is confirmed by semiconductor α-spectrometry. The nuclide yields are shown to equal 70-90%

  7. Application of activation analysis for determination of some elements in cassiterite samples

    International Nuclear Information System (INIS)

    Armelin, Maria Jose Aguirre

    1978-01-01

    This work consists in the development of an analytical method using activation by thermal neutrons for the determination of some minor elements and traces present in cassiterite (tin ore). This method was then applied to determine these elements in samples of cassiterite from different regions of Brazil. An analysis was made of the mineralogy characteristic of cassiterite as well as of the minerals most commonly associated with it. Four main types of interference were found to occur in the analysis by activation of trace elements in samples of cassiterite. The method involves the analysis without chemical separation for the determination of some elements and the analysis with chemical separation for the determination of other elements. The steps involved in both types of analysis are described. In the analysis with chemical separation the matrix element (tin) is separated by distillation in an H 2 SO 4 -HBr medium, after fusion of the ore with Na 2 O 2 . Arsine and antimony are determined in the distilled, whereas some lanthanide elements and uranium are determined in the distillation residue by separating them as a group by precipitation with lanthanum fluoride. A discussion on the precision, accuracy and sensibility of the method is also included. (author)

  8. Technical papers presented at a DOE meeting on criteria for cleanup of transuranium elements in soil

    International Nuclear Information System (INIS)

    1984-09-01

    Transuranium element soil contamination cleanup experience gained from nuclear weapons accidents and cleanup at Eniwetok Atoll was reviewed. Presentations have been individually abstracted for inclusion in the data base

  9. Determining arsenic in elemental antimony containing selenium and tellurium

    International Nuclear Information System (INIS)

    Mogileva, M.G.; Kozlova, E.L.

    1986-01-01

    The authors have developed a method of determining arsenic in metallic antimony containing selenium, tellurium, and mercury, in which they isolated it in elementary form for separation from the antimony and the associated elements (silicon and phosphorus), followed by colorimetric determination of the arsenic from arsenic-molbdenum blue. The reducing agents to reduce the arsenic were sodium hypophosphite and tin(II) chloride, which do not reduce antimony and which do not interfere with the determination. This method of determining arsenic in metallic antimony without preliminary separation of the selenium and tellurium is in no way inferior in accuracy to the method given in All-Union State Standard (GOST) 1367.4-83

  10. Determination of rare earth elements by liquid chromatography/inductively coupled plasma atomic emission spectrometry

    International Nuclear Information System (INIS)

    Yoshida, K.; Haraguchi, H.

    1984-01-01

    Inductively coupled plasma atomic emission spectrometry (ICP-AES) interfaced with high-performance liquid chromatography (HPLC) has been applied to the determination of rare earth elements. ICP-AES was used as an element-selective detector for HPLC. The separation of rare earth elements with HPLC helped to avoid erroneous analytical results due to spectral interferences. Fifteen rare earth elements (Y and 14 lanthanides) were determined selectively with the HPLC/ICP-AES system using a concentration gradient method. The detection limits with the present HPLC/ICP-AES system were about 0.001-0.3 μg/mL with a 100-μL sample injection. The calibration curves obtained by the peak height measurements showed linear relationships in the concentration range below 500 μg/mL for all rare earth elements. A USGS rock standard sample, rare earth ores, and high-purity lanthanide reagents (>99.9%) were successfully analyzed without spectral interferences

  11. English presentation of each data element of articles in serial publications in Japan

    International Nuclear Information System (INIS)

    Narui, Shigeko; Izawa, Michiyo; Naramoto, Miyoko; Kajiro, Tadashi

    1981-01-01

    Texts and several data elements were surveyed by extracting 1,000 articles from inputs to the INIS. Rates of English presentation in journals were as the following: texts 38%, abstracts 72%, keywords 27%, titles 88%, personal authors 90% and affiliations 79%. Also, articles describing all data elements in English were 25% and articles without keywords in English 68%. As a result of the survey, private organizations and publishers give priority of access data elements to body of the works, universities and public agencies priority of the works, and associations both phases, comparing with the rates of English presentation between texts and the access data elements. The English presentation in technical reports were as follows: texts 46%, abstracts 83%, keywords 53%, titles 88%, personal authors 86%, corporate authors 97%, and affiliations 85%. (author)

  12. Determination of the elemental content in cigarettes by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Metwally, E.

    2001-01-01

    Cigarette smoking, a worldwide habit, has a very bad and hazardous effect on the human body. Neutron activation analysis technique is used in the present study. Different kinds of cigarette brands have been collected from local and foreign markets representing ten countries all over the world. All the selected samples are irradiated in first Ins has reactor, ER-1 in Egypt. A comprehensive study of the elemental content in cigarette samples under investigation has been carried out. Concentrations of the polluting elements, tracers' content and more than twenty elements have been determined. The obtained data resulting from the present work are discussed

  13. Determination and evaluation of toxic elements in Chinese foodstuffs

    International Nuclear Information System (INIS)

    Sun Laiyan; Lu Fengying; Zhou Wenping; Zhen Houxi; Su Rongwei; Liao Qingshang; Li Xuezeng; Wang Huaihui

    1988-01-01

    The concentrations of toxic elements As, Br, Cr, Cu, Pb, Se and Zn in various foodstuffs collected in Beijing, Shanghai, Xian and Wuhan were determined using neutron activation analysis (NAA) and atomic absorption spectrometry (AAS) methods were obtained with high or medium precision. According to the average daily intake of various foods, the daily intake of these toxic elements were estimated for each person in the four cities. They (in microgram) were 42.6, 166.3, 1738, 106.8, 7939, 1145 and 67.1 respectively for As, Cr, Cu, Se, Zn, Br and Pb in Beijing, 52.2, 167, 1213, 91.5, 6026, 519 and 89.9 in Shanghai, 46.2, 184, 1782, 119.2, 8729, 1132 and 133.4 in Xian, and 63.2, 142.1, 1556, 76.9, 7882, 528 and 73.7 in Wuhan. (author). 2 refs, 12 tabs

  14. 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)

  15. 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

  16. Determination of some elements in Ageratum conyziodes, a tropical medicinal plant, using instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Dim, L.A.; Funtua, I.I.; Umar, I.M.; Gwozdz, R.

    2004-01-01

    Instrumental neutron activation analysis was utilized for the multielemental determination of elements in the roots of Ageratum conyzoides, a tropical medicinal plant that is used locally for the cure of various diseases in Nigeria. The concentrations of Al, Ba, Br, Ca, Co, Cr, Fe, K, Mg, Mn, Na, Rb, Sc, Sr, V and Zn were analyzed with the 250 kW Triga Reactor at the Atominstitut, Vienna. The essential elements K, Na, Ca, Fe, Mg, Mn and Zn and the non-essential elements Al, Ba, Sr and Rb are present in significant concentrations. Other elements including Co, Cr, Sc and V are present at trace levels. The likely implication of these elements in restoring and maintaining good health is discussed. Quality control on the measurements was carried out by analyzing standard reference materials alongside the samples. (author)

  17. 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.

  18. Neutron physics calculation for WWER-1000 absorber element lifetime determination

    International Nuclear Information System (INIS)

    Kurakin, K.Yu.; Kushmanov, S.A.

    2009-01-01

    Absorber element with compound absorber has been operating in WWER-1000 power units since 1995. AE design meets operating organizations requirements for reliability, service life (to 10 years) and safety functions. Extension of AE service life up to 20 - 30 years by the complex of calculation and experimental work is an important problem of WWER new designs development. The paper deals with the issues related to calculation determination of main factors that influence AE service life limitation - neutron flux and fluence onto absorbing and structural materials during extended service life. (Authors)

  19. Improved determination of hadron matrix elements using the variational method

    International Nuclear Information System (INIS)

    Dragos, J.; Kamleh, W.; Leinweber, D.B.; Zanotti, J.M.; Rakow, P.E.L.; Young, R.D.; Adelaide Univ.

    2015-11-01

    The extraction of hadron form factors in lattice QCD using the standard two- and three-point correlator functions has its limitations. One of the most commonly studied sources of systematic error is excited state contamination, which occurs when correlators are contaminated with results from higher energy excitations. We apply the variational method to calculate the axial vector current g A and compare the results to the more commonly used summation and two-exponential fit methods. The results demonstrate that the variational approach offers a more efficient and robust method for the determination of nucleon matrix elements.

  20. Determination of the elemental composition of copper and bronze objects by neutron activation analysis

    International Nuclear Information System (INIS)

    Hoelttae, P.; Rosenberg, R.J.

    1987-01-01

    A method for the elemental analysis of copper and bronze objects is described. Na, Co, Ni, Cu, Zn, As, Ag, Sn, Sb, W, Ir and Au are determined through instrumental neutron activation analysis. Mg, Al, V, Ti and Mn are determined after chemical separation using anionic exchange. The detection limits for a number of other elements are also given. Results for NBS standard reference materials are presented and the results are compared with the recommended values. The agreement is good. The results of the analysis of five ancient bronze and two copper objects are also presented. (author) 3 refs.; 4 tabs

  1. Determination of the elemental composition of copper and bronze objects by neutron activation analysis

    International Nuclear Information System (INIS)

    Hoelttae, P.; Rosenberg, R.J.

    1986-01-01

    A method for the elemental analysis of copper and bronze objects is described. Na, Co, Ni, Cu, Zn, As, Ag, Sn, Sb, W, Ir and Au are determined through instrumental neutron activation analysis. Mg, Al, V, Ti and Mn are determined after chemical separation using anionic exchange. The detection limits for a number of other elements are also given. Results for NBS standard reference materials are presented and the results compared with the recommended values. The agreement is good. The results of the analysis of five ancient bronze and two copper objects are presented. (author)

  2. A nondestructive testing device for determining 235U enrichment in power reactor fuel elements

    International Nuclear Information System (INIS)

    Liu Lanhua; Liu Nangai

    1990-07-01

    The development and application of a nondestructive testing device are presented, which is used for determining the 235 U enrichment in the mixed fuel of fuel elements with UO 2 pellets. The testing efficiency is improved because the passive gamma ray method and a hole-bored NaI crystal and four channel multichannel analyzer are used. The false discrimination rate is reduced as the average comparing method is taken. This device is simple in structure and easy in operation. It has provided a new testing tool for the fuel elements production in China. This device has successfully been used in Qinshan Nuclear Power Plant in testing its fuel elements

  3. Determination of the Reliability Function of Nonredundant Element of Power Object

    International Nuclear Information System (INIS)

    Namgaladze, D.; Kiziria, T.

    2007-01-01

    At considering the reliability indices of the system element with recovery, the time of operation and recovery is usually accounted for. But, in practice, there often occur the situations when, after the failure of the system (or its element), it takes considerable time to begin repairing (time for revealing the damages, time for organization of repairing work, delivery of spare parts etc.). The total dead time is called the waiting time. In the present work, the reliability indices of the element of power object with account for the waiting time are determined analytically by using Markovian processes. (author)

  4. Distance-based relative orbital elements determination for formation flying system

    Science.gov (United States)

    He, Yanchao; Xu, Ming; Chen, Xi

    2016-01-01

    The present paper deals with determination of relative orbital elements based only on distance between satellites in the formation flying system, which has potential application in engineering, especially suited for rapid orbit determination required missions. A geometric simplification is performed to reduce the formation configuration in three-dimensional space to a plane. Then the equivalent actual configuration deviating from its nominal design is introduced to derive a group of autonomous linear equations on the mapping between the relative orbital elements differences and distance errors. The primary linear equations-based algorithm is initially proposed to conduct the rapid and precise determination of the relative orbital elements without the complex computation, which is further improved by least-squares method with more distance measurements taken into consideration. Numerical simulations and comparisons with traditional approaches are presented to validate the effectiveness of the proposed methods. To assess the performance of the two proposed algorithms, accuracy validation and Monte Carlo simulations are implemented in the presence of noises of distance measurements and the leader's absolute orbital elements. It is demonstrated that the relative orbital elements determination accuracy of two approaches reaches more than 90% and even close to the actual values for the least-squares improved one. The proposed approaches can be alternates for relative orbit determination without assistance of additional facilities in engineering for their fairly high efficiency with accuracy and autonomy.

  5. Element determination of fine particles in environmental aerosols using PIXE

    International Nuclear Information System (INIS)

    Garcia O, B.; Aldape U, F.

    2007-01-01

    The Mexico city is classified as one of the more populated cities of the world which presents a decrease in the air quality and that gives place to a severe problematic in atmospheric pollution. To cooperate in the solution of this problem it is necessary to carry out studies that allow a better knowledge of the atmosphere of the city. This study presents the results of a monitoring campaign of fine particle carried out from September 21 to December 12, 2001 in three sites of the Mexico City center area. The samples were collected every third day with a collector type unit of heaped filters (Gent). The analysis of these samples was carried out in the 2 MV accelerator of the National Institute of Nuclear Research (ININ) applying the PIXE technique and with this analysis its were identified in the samples approximately 15 elements in each one of the 3 sites and was calculated the concentration in that its were present. With these results a database was created and by means of it mathematical treatment the Enrichment factor (FE), the time series of each element and the multiple correlation matrix were evaluated. The obtained results showed that the Civil Registration site (Salto del Agua) it was the more polluted coinciding that to a bigger concentration of activities a bigger increase in the pollution is generated. (Author)

  6. 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)

  7. Age determination of Precambrian rocks from Greenland: past and present

    International Nuclear Information System (INIS)

    Karlsbeek, F.

    1997-01-01

    For Precambrian rocks as well as for younger igneous intrusions, precise ages can only be obtained by isotopic analysis of minerals or rocks. Isotopic (radiometric) age determination of Greenland rocks began in the early 1960s and has continued since with gradually improving methods. In this contribution, the development of geochronological knowledge of the Precambrian of Greenland is described in historical perspective, and an outline of new results is given. The history of geochronology can be roughly divided into three periods: 1) a period of single-sample K-Ar and Rb-Sr mineral or whole-rock age determinations; 2) a time when most ages were determined with the help of Rb-Sr and Pb-Pb whole-rock isochrones and multi-grain zircon U-Pb isotope data; 3) the present, where 'single' zircon U-Pb data are the preferred method to obtain rock ages. These stages in the development of radiometric dating methods partly overlap in time, and each has yielded very significant contributions to the knowledge of Precambiran evolution in Greenland. (EG)

  8. Determination of elements in ayurvedic medicinal plants by AAS

    International Nuclear Information System (INIS)

    Teerthe, Santoshkumar S.; Kerur, B. R.

    2015-01-01

    India has a rich country for the uses of Ayurvedic medicinal plants for treatment and also the north- Karnataka boasts an unparallel diversity of medicinal plants. The present study attempts to estimate and compare the level of trace and heavy metals in some selected leaves and root samples of Ayurvedic medicinal plants such as Mg, Al, K, Cr, Mn, Fe, Cu, Zn, and Cd. The samples are collected from different places of North-Karnataka regions and sample solutions prepared as the ratio of 1:25:25+950ml=1000ppm.the trace and heavy elemental concentration was estimated using Atomic Absorption Spectrometric (AAS) Method. The average concentrations of Mg, Mn, Fe and Zn, are ranging from 2ppm to 5250.2ppm and potassium (K) has more concentration as compare to all other. The other elements likes Al, Cr, Cu, and Cd were also estimed and presented in the table. Therefore, these medicinal plants are rich in some essential minerals, especially K, Mg, Mn, Fe and Zn which are essential for human health

  9. Determination of elements in ayurvedic medicinal plants by AAS

    Energy Technology Data Exchange (ETDEWEB)

    Teerthe, Santoshkumar S.; Kerur, B. R., E-mail: kerurbrk@yahoo.com [Department of Physics, Gulbarga University, Gulbarga, and Karnataka, India – 585106 (India)

    2015-08-28

    India has a rich country for the uses of Ayurvedic medicinal plants for treatment and also the north- Karnataka boasts an unparallel diversity of medicinal plants. The present study attempts to estimate and compare the level of trace and heavy metals in some selected leaves and root samples of Ayurvedic medicinal plants such as Mg, Al, K, Cr, Mn, Fe, Cu, Zn, and Cd. The samples are collected from different places of North-Karnataka regions and sample solutions prepared as the ratio of 1:25:25+950ml=1000ppm.the trace and heavy elemental concentration was estimated using Atomic Absorption Spectrometric (AAS) Method. The average concentrations of Mg, Mn, Fe and Zn, are ranging from 2ppm to 5250.2ppm and potassium (K) has more concentration as compare to all other. The other elements likes Al, Cr, Cu, and Cd were also estimed and presented in the table. Therefore, these medicinal plants are rich in some essential minerals, especially K, Mg, Mn, Fe and Zn which are essential for human health.

  10. 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.)

  11. 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.

  12. Specificity determinants for the abscisic acid response element.

    Science.gov (United States)

    Sarkar, Aditya Kumar; Lahiri, Ansuman

    2013-01-01

    Abscisic acid (ABA) response elements (ABREs) are a group of cis-acting DNA elements that have been identified from promoter analysis of many ABA-regulated genes in plants. We are interested in understanding the mechanism of binding specificity between ABREs and a class of bZIP transcription factors known as ABRE binding factors (ABFs). In this work, we have modeled the homodimeric structure of the bZIP domain of ABRE binding factor 1 from Arabidopsis thaliana (AtABF1) and studied its interaction with ACGT core motif-containing ABRE sequences. We have also examined the variation in the stability of the protein-DNA complex upon mutating ABRE sequences using the protein design algorithm FoldX. The high throughput free energy calculations successfully predicted the ability of ABF1 to bind to alternative core motifs like GCGT or AAGT and also rationalized the role of the flanking sequences in determining the specificity of the protein-DNA interaction.

  13. Simplified Qualitative Discrete Numerical Model to Determine Cracking Pattern in Brittle Materials by Means of Finite Element Method

    OpenAIRE

    Ochoa-Avendaño, J.; Garzon-Alvarado, D. A.; Linero, Dorian L.; Cerrolaza, M.

    2017-01-01

    This paper presents the formulation, implementation, and validation of a simplified qualitative model to determine the crack path of solids considering static loads, infinitesimal strain, and plane stress condition. This model is based on finite element method with a special meshing technique, where nonlinear link elements are included between the faces of the linear triangular elements. The stiffness loss of some link elements represents the crack opening. Three experimental tests of bending...

  14. Determinants of late presentation for induced abortion care.

    Science.gov (United States)

    Waddington, Ashley; Hahn, Philip M; Reid, Robert

    2015-01-01

    To determine whether demographic or patient factors contribute to later presentation (10 to 12 weeks' gestational age) for induced abortion in a Canadian abortion clinic. Women attending a hospital-based abortion clinic between April and September 2012 were asked to complete a survey. The characteristics of women who presented early (EPs; gestational age abortion" (26.45% for EPs, 32.4% for LPs; P = 0.421), LPs were more likely to report that discouragement "caused a delay in making arrangements" (45.5% vs. 16.7%; P = 0.019). Of women who had access to a primary care provider, it was more common for the primary care provider to be aware of the pregnancy among LPs than among EPs (80.6% vs. 63.1%; P = 0.015). Some women delay presenting for abortion because of discouragement from friends and family. It is unclear whether there are educational or policy interventions that can have an impact on this delay, and this warrants further study. There may be ways of addressing the delay in referral by primary care providers. Further study into the causes for delay in referral for abortion is warranted.

  15. 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

  16. Determination os essential elements in diet and light foods using neutron activation analysis

    International Nuclear Information System (INIS)

    Ito, Gerson Hideo; Maihara, Vera Akiko

    2007-01-01

    The object of this study was to determine essential elements on the diet and light foods and their normal similar through the neutron activation analysis (NAA) and to compare their results. Samples of sweetning, cappuccino, gelatine and chocolate collected at the Sao Paulo commerce were irradiated by a period of 8 hours, under a 10 12 n cm -2 s -1 thermal neutron flux at the IEA-R1 research reactor - IPEN/CNEN-SP, Brazil, together with reference materials and elementary standards, for the determination the concentrations of Br, Ca, Cr, Co, K, Na, Fe, Se and Zn. The obtained results shown that the diet gelatine samples presented concentrations higher for determined elements related to the light and normal gelatines samples. Compared with cappucino samples there was not differences among the concentrations of the determined elements, excepted the element Cr for the cappuccino light. For the chocolate light they presents higher values related to the normal type. The sweetening did not present differences among the samples. (author)

  17. Determination of heterogeneous medium parameters by single fuel element method

    International Nuclear Information System (INIS)

    Veloso, M.A.F.

    1985-01-01

    The neutron pulse propagation technique was employed to study an heterogeneous system consisting of a single fuel element placed at the symmetry axis of a large cylindrical D 2 O tank. The response of system for the pulse propagation technique is related to the inverse complex relaxation length of the neutron waves also known as the system dispersion law ρ (ω). Experimental values of ρ (ω) were compared with the ones derived from Fermi age - Diffusion theory. The main purpose of the experiment was to obtain the Feinberg-Galanin thermal constant (γ), which is the logaritmic derivative of the neutron flux at the fuel-moderator interface and a such a main input data for heterogeneous reactor theory calculations. The γ thermal constant was determined as the number giving the best agreement between the theoretical and experimental values of ρ (ω). The simultaneous determination of two among four parameters η,ρ,τ and L s is possible through the intersection of dispersion laws of the pure moderator system and the fuel moderator system. The parameters τ and η were termined by this method. It was shown that the thermal constant γ and the product η ρ can be computed from the real and imaginary parts of the fuel-moderator dispersion law. The results for this evaluation scheme showns a not stable behavior of γ as a function of frequency, a result not foreseen by the theoretical model. (Author) [pt

  18. Determination of essential elements in herbal extracts by neutron activation analysis

    International Nuclear Information System (INIS)

    Francisconi, Lucilaine S.; Goncalves, Rodolfo D.M.R.; Silva, Paulo S.C. da

    2013-01-01

    Different types of therapies have been introduced as an alternative treatment to various types of human disorders, among them,the use of herbal teas have been highlighted due to its low cost, easiness of acquisition and administration. The aim of this study was to evaluate the concentrations of the elements As, Ba, Br, Ca, Co, Cr, Cs, Fe, Hf, K, Na, Rb, Sb, Sc, Se, Ta, Th, U, Zn and Zr by neutron activation analysis in extracts of medicinal plants whose use is regulated by ANVISA. The relevance of this analysis is justified by the need of contributing to the recommendation of these plants as secure sources of mineral elements both for therapeutic and dietary purpose. The technique showed good sensitivity in determining the appropriate concentration of all the determined elements. Elements potentially toxic were found at concentration that do not present threats to the organism and the elements that present important roles in metabolism were determined at concentrations that can assist both therapeutic and nutritional purposes. (author)

  19. Determination of essential elements in herbal extracts by neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Francisconi, Lucilaine S.; Goncalves, Rodolfo D.M.R.; Silva, Paulo S.C. da, E-mail: lfrancisconi@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    Different types of therapies have been introduced as an alternative treatment to various types of human disorders, among them,the use of herbal teas have been highlighted due to its low cost, easiness of acquisition and administration. The aim of this study was to evaluate the concentrations of the elements As, Ba, Br, Ca, Co, Cr, Cs, Fe, Hf, K, Na, Rb, Sb, Sc, Se, Ta, Th, U, Zn and Zr by neutron activation analysis in extracts of medicinal plants whose use is regulated by ANVISA. The relevance of this analysis is justified by the need of contributing to the recommendation of these plants as secure sources of mineral elements both for therapeutic and dietary purpose. The technique showed good sensitivity in determining the appropriate concentration of all the determined elements. Elements potentially toxic were found at concentration that do not present threats to the organism and the elements that present important roles in metabolism were determined at concentrations that can assist both therapeutic and nutritional purposes. (author)

  20. 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.)

  1. TRIGA fuel element burnup determination by measurement and calculation

    International Nuclear Information System (INIS)

    Zagar, T.; Ravnik, M.; Persic, A.; Jeraj, R.

    2000-01-01

    To estimate the accuracy of the fuel element burnup calculation different factors influencing the calculation were studied. To cover different aspects of burnup calculations, two in-house developed computer codes were used in calculations. The first (TRIGAP) is based on a one-dimensional two-group diffusion approximation, and the second (TRIGLAV) is based on a two-dimensional four-group diffusion equation. Both codes use WIMSD program with different libraries forunit-cell cross section data calculation. The burnup accumulated during the operating history of the TRIGA reactor at Josef Stefan Institute was calculated for all fuel elements. Elements used in the core during this period were standard SS 8.5% fuel elements, standard SS 12% fuel elements and highly enriched FLIP fuel elements. During the considerable period of operational history, FLIP and standard fuel elements were used simultaneously in mixed cores. (authors)

  2. 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)

  3. The use of voltammetry for determining uranium and associated elements in compounds of nuclear interest

    International Nuclear Information System (INIS)

    Carvalho, F.M.S. de.

    1988-01-01

    The determination of uranium and some trace elements found as impurities in nuclear materials by the voltammetric technique using the hanging mercury drop electrode is presented. Emphasis is given to the determination of uranium, of major interest. Europium and ytterbium are simultaneously determined in fractions of individual lanthanides. A procedure for the simultaneous determination of copper, cadmium, nickel and zinc in water, industrial effluents and uranium compounds is discussed. The advantage of the procedure is its simplicity and easiness of execution, with excellent precision and accuracy. (author) [pt

  4. A proposal for a determination method of element division on an analytical model for finite element elastic waves propagation analysis

    International Nuclear Information System (INIS)

    Ishida, Hitoshi; Meshii, Toshiyuki

    2010-01-01

    This study proposes an element size selection method named the 'Impact-Meshing (IM) method' for a finite element waves propagation analysis model, which is characterized by (1) determination of element division of the model with strain energy in the whole model, (2) static analysis (dynamic analysis in a single time step) with boundary conditions which gives a maximum change of displacement in the time increment and inertial (impact) force caused by the displacement change. In this paper, an example of application of the IM method to 3D ultrasonic wave propagation problem in an elastic solid is described. These examples showed an analysis result with a model determined by the IM method was convergence and calculation time for determination of element subdivision was reduced to about 1/6 by the IM Method which did not need determination of element subdivision by a dynamic transient analysis with 100 time steps. (author)

  5. 77 FR 1434 - Proposed Confidentiality Determinations for Data Elements Under the Mandatory Reporting of...

    Science.gov (United States)

    2012-01-10

    ... Fluorinated Gas Production....... 325120 Industrial gases manufacturing facilities. Electrical Equipment Use... Proposed Confidentiality Determinations for Data Elements Under the Mandatory Reporting of Greenhouse Gases...-proposes confidentiality determinations for the data elements under the Mandatory Greenhouse Gas Reporting...

  6. Fundamental quantification procedure for total reflection X-ray fluorescence spectra analysis and elements determination

    International Nuclear Information System (INIS)

    Wegrzynek, D.; Holynska, B.

    1997-01-01

    A method for the determination of the concentrations of elements in particulate-like samples measured in total reflection geometry is proposed. In the proposed method the fundamental parameters are utilized for calculating the sensitivities of elements and an internal standard is used to account for the unknown mass per unit area of a sample and geometrical constant of the spectrometer. The modification of the primary excitation spectrum on its way to a sample has been taken into consideration. The concentrations of the elements to be determined are calculated simultaneously with the spectra deconvolution procedure. In the process of quantitative analysis the intensities of all X-ray peaks corresponding to K and L-series lines present in the analyzed spectrum are taken into account. (Author)

  7. Determination of 22 elements in Marine Environmental Samples in special areas at the South of Vietnam

    International Nuclear Information System (INIS)

    Nguyen Ngoc Tuan; Nguyen Giang; Nguyen Thanh Tam; Truong Phuong Mai

    2007-01-01

    In 2007 year, we continued to determine the contents of 22 elements in marine environmental samples such as marine sediment, seawater and marine creature. The methods for the determination of elements in these objects are Neutron Activation Analysis and Atomic Absorption Spectrophotometer. The obtained analytical results are a database to monitor marine environmental pollution and to evaluate the impact of exploitation of rare earth- radioactive ores near by the sea coast; exploitation of crude oil in offshore and technology activities at the south of Vietnam in the future. The analytical results of toxic and trace element contents are also to attend the Forum for Nuclear Cooperation of Asia (FNCA) in which Vietnam is one of nine member counties. The analytical results have been presented in the FNCA 2007 workshop on utilization of the research reactor from 28 September-02 October in Serpong, Indonesia. (author)

  8. Determination of elements in citrus leaves; Dosage des elements dans les feuilles de citrus

    Energy Technology Data Exchange (ETDEWEB)

    Masozera, C.; Compernolle, G. van; Brandstetr, J.; Krivanek, M. [Centre nucléaire TRICO, Kinshasa (Congo, The Democratic Republic of the); Université Lovanium, Kinshasa (Congo, The Democratic Republic of the)

    1970-01-15

    In many agricultural stations and farms most of the problems encountered generally reduce to questions of diminished yield. This may be due to a number of factors, including soil exhaustion and the application of fertilizers of unsuitable formula. The chemical impoverishment of the soil is due to the leaching-out phenomenon, i- e. the washing out of bases, and to the ''exportation'' of fertilizer elements in the form of crops in years when nothing has been returned to the soil. These losses have a particularly adverse effect if the parent rock does not contain sufficient mineral reserves to compensate for them by a slow alteration process. Such impoverishment is revealed by soil and foliar analyses. The authors have attempted to determine the content in citrus plants of the following elements: Mn, P, Cu, Cl and K (the latter on three samples only). After collection, the samples are treated by Bransolten's method (Rapport de Recherche TRICO № 15/1968), dried for at least 12 hours at 105°C, followed by pulverization of the leaves, after which the determination is carried out. The determination of Mn and Cl is very simple, as is that of Cu. The latter is determined by activation with slow neutrons in order to avoid Zn formation. The phosphorus content is determined by measuring the beta-radiation emitted by the radioactive elements. In this case particular precautions must be taken to ensure that the same layer is used for the samples and the standards, since beta-radiation is absorbed by these layers. For the K and Na determinations thermal neutrons are used for activation and a Ge(Li) detector for measurement of the gamma-spectra. Because of the high resolution of the detector, the two elements can be determined without separation. (author) [French] La plupart des problèmes que l’on rencontre dans plusieurs stations ou exploitations agricoles se résument généralement à une diminution de rendement. Cette dernière peut être provoquée par plusieurs

  9. Monitoring of toxic elements present in sludge of industrial waste using CF-LIBS.

    Science.gov (United States)

    Kumar, Rohit; Rai, Awadhesh K; Alamelu, Devanathan; Aggarwal, Suresh K

    2013-01-01

    Industrial waste is one of the main causes of environmental pollution. Laser-induced breakdown spectroscopy (LIBS) was applied to detect the toxic metals in the sludge of industrial waste water. Sludge on filter paper was obtained after filtering the collected waste water samples from different sections of a water treatment plant situated in an industrial area of Kanpur City. The LIBS spectra of the sludge samples were recorded in the spectral range of 200 to 500 nm by focusing the laser light on sludge. Calibration-free laser-induced breakdown spectroscopy (CF-LIBS) technique was used for the quantitative measurement of toxic elements such as Cr and Pb present in the sample. We also used the traditional calibration curve approach to quantify these elements. The results obtained from CF-LIBS are in good agreement with the results from the calibration curve approach. Thus, our results demonstrate that CF-LIBS is an appropriate technique for quantitative analysis where reference/standard samples are not available to make the calibration curve. The results of the present experiment are alarming to the people living nearby areas of industrial activities, as the concentrations of toxic elements are quite high compared to the admissible limits of these substances.

  10. 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

  11. Elemental content in cigarette components and its distribution as determined by neutron activation analysis

    International Nuclear Information System (INIS)

    Metwally, Y.E.

    2003-01-01

    Cigarette smoking, a world-wide habit. Has a very bad and hazardous effects on the human body. In the present study, different kinds of cigarette brands have been collected from local and foreign markets representing ten countries all over the world. All the selected samples were irradiated in first Inshas reactor (IR-1) in Egypt. A comprehensive study of the elemental contents in cigarette samples under investigation has been carried out by using neutron activation analysis technique. Concentrations of the polluting elements and tracer contents of cigarette tobacco have been determined. The elemental distribution of the component (tobacco. ash. filter before and after smoking and wrapping paper) of some kinds of cigarettes has been studied. The obtained data resulting from the present work were discussed

  12. Large number of ultraconserved elements were already present in the jawed vertebrate ancestor.

    KAUST Repository

    Wang, Jianli; Lee, Alison P; Kodzius, Rimantas; Brenner, Sydney; Venkatesh, Byrappa

    2009-01-01

    Stephen (2008) identified 13,736 ultraconserved elements (UCEs) in placental mammals and investigated their evolution in opossum, chicken, frog, and fugu. They found that there was a massive expansion of UCEs during tetrapod evolution and the substitution rate in UCEs showed a significant decline in tetrapods compared with fugu, suggesting they were exapted in tetrapods. They considered it unlikely that these elements are ancient but evolved at a higher rate in teleost fishes. In this study, we investigated the evolution of UCEs in a cartilaginous fish, the elephant shark and show that nearly half the UCEs were present in the jawed vertebrate ancestor. The substitution rate in UCEs is higher in fugu than in elephant shark, and approximately one-third of ancient UCEs have diverged beyond recognition in teleost fishes. These data indicate that UCEs have evolved at a higher rate in teleost fishes, which may have implications for their vast diversity and evolutionary success.

  13. Large number of ultraconserved elements were already present in the jawed vertebrate ancestor.

    KAUST Repository

    Wang, Jianli

    2009-03-01

    Stephen (2008) identified 13,736 ultraconserved elements (UCEs) in placental mammals and investigated their evolution in opossum, chicken, frog, and fugu. They found that there was a massive expansion of UCEs during tetrapod evolution and the substitution rate in UCEs showed a significant decline in tetrapods compared with fugu, suggesting they were exapted in tetrapods. They considered it unlikely that these elements are ancient but evolved at a higher rate in teleost fishes. In this study, we investigated the evolution of UCEs in a cartilaginous fish, the elephant shark and show that nearly half the UCEs were present in the jawed vertebrate ancestor. The substitution rate in UCEs is higher in fugu than in elephant shark, and approximately one-third of ancient UCEs have diverged beyond recognition in teleost fishes. These data indicate that UCEs have evolved at a higher rate in teleost fishes, which may have implications for their vast diversity and evolutionary success.

  14. Determination of certain elements in camel's milk by neutron activation analysis

    International Nuclear Information System (INIS)

    Bejey, M.A.; Markus, W.M.; Etwir, R.H.

    1995-01-01

    Natural milk samples were analysed by instrumental neutron activation analysis (INAA) for (Mn, Fe, Zn, Co, Cr, Rb, Br, I). These samples were collected from different regions of libya co-operation with camel,s research center in tripoli. In our laboratories trace elements in human and milk powder samples have been, also determined using the (INAA) technique. The concentration level of the elements of interest of interest are in agreement to within 10% with obtained values for human and powder milk, except for the concentration of Br, I, and Rb which were found to be higher in camel's milk results of this investigation will be presented. 6 figs

  15. Selective determination of plutonium and transplutonic elements (Am, Cm) in feces ashes

    International Nuclear Information System (INIS)

    Ballada, J.; Verry, M.; Daburon, M.L.; Jeanmaire, L.

    1983-02-01

    A technique has been developed for the selective determination of the main transplutonic elements of the fuel cycle in feces ashes. The natural elements (U, Ra, Th and their isotopes) usually present in the human diet, are eliminated. Plutonium separation is carried out in a classical way by ion exchange resin. After elimination of U and Th, Am-Cm are collected on a millipore filter for α spectrometry or global counting. Yields are 95% (σ = 4) for Pu and 81.7% (σ = 6,2) for Am-Cm [fr

  16. Determination of certain elements in camel`s milk by neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Bejey, M A; Markus, W M; Etwir, R H [Tajoura Nuclear research Center, P.O. Box 30878, Tajoura, (Libyan Arab Jamahiriya)

    1995-10-01

    Natural milk samples were analysed by instrumental neutron activation analysis (INAA) for (Mn, Fe, Zn, Co, Cr, Rb, Br, I). These samples were collected from different regions of libya co-operation with camel,s research center in tripoli. In our laboratories trace elements in human and milk powder samples have been, also determined using the (INAA) technique. The concentration level of the elements of interest of interest are in agreement to within 10% with obtained values for human and powder milk, except for the concentration of Br, I, and Rb which were found to be higher in camel`s milk results of this investigation will be presented. 6 figs.

  17. 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

  18. Spectrofluorimetric determination of rare earth elements using solidmatrix

    International Nuclear Information System (INIS)

    Suh, I.S.; Chi, K.Y.

    1982-01-01

    In this experiment, rare earth elements are separated from uranium by using the alumina column, anion exchange resin column, and 20% TOA in xylene and fluorescence characteristics were found in the solid matrix to analyze these elements without preseparation from each other. It becomes clear that the YVO 4 matrix is more sensitive than the Y 2 O 3 matrix when the red filter is used to minimized the second order peak intensity. And micro quantity of the rare earth elements in the yellow cake are analyzed by the using of the YVO 4 soid matrix. (Author)

  19. A survey of the determination of the platinum group elements.

    Science.gov (United States)

    Kallmann, S

    1987-08-01

    The platinum-group metals (PGMs), Ru, Rh, Pd, Os, Ir and Pt, are widely used as catalysts in petroleum and chemical processes. They find wide applications in automotive exhaust-gas control converters and are of immense importance to the electronics industry. They are found in many items of jewellery and serve to an increasing extent as a form of investment. The PGMs are extracted in minute quantities from a limited number of ores, found mainly in S. Africa and the USSR. They are concentrated and separated from each other by elaborate chemical processes. Because of their great intrinsic value (Pt $650 per oz; Rh $1400 per oz), the recycling of the PGMs from literally hundreds of different forms of scrap is an essential factor in the overall management of the PGM economy. In this survey emphasis is placed on the need to tailor the analytical method according to (a) the environment in which the PGMs occur, (b) the individual PGM concentrations, and (c) the desired sensitivity and precision. The factors which determine the choice of chemical, physicochemical and/or instrumental approaches are discussed. They are further commented on in extensive presentations of dissolution and separation techniques and methods for the final measurement of individual PGMs. Appendices are provided which present the compositions and sources of the products most frequently encountered in PGM analysis, along with information on methods of decomposition, separations required, type of separation, and final determination.

  20. 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)

  1. 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)

  2. 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

  3. Establishing a protocol for element determination in human nail clippings by neutron activation analysis

    International Nuclear Information System (INIS)

    Sanches, Thalita Pinheiro; Saiki, Mitiko

    2011-01-01

    Human nail samples have been analyzed to evaluate occupational exposure, nutritional status and to diagnose certain diseases. However, sampling and washing protocols for nail analyses vary from study to study not allowing comparisons between studies. One of the difficulties in analyzing nail samples is to eliminate only surface contamination without removing elements of interest in this tissue. In the present study, a protocol was defined in order to obtain reliable results of element concentrations in human nail clippings. Nail clippings collected from all 10 fingers or toes were previously pre cleaned using an ethyl alcohol solution to eliminate microbes. Then, the clippings were cut in small pieces and submitted to different reagents for washing by shaking. Neutron activation analysis (NAA) was applied for nail samples analysis which consisted of irradiating aliquots of samples together with synthetic elemental standards in the IEA-R1 nuclear research reactor followed by gamma ray spectrometry. Comparisons made between the results obtained for nails submitted to different reagents for cleaning indicated that the procedure using acetone and Triton X100 solution is more effective than that of nitric acid solution. Analyses in triplicates of a nail sample indicated results with relative standard deviations lower than 15% for most of elements, showing the homogeneity of the prepared sample. Qualitative analyses of different nail polishes showed that the presence of elements determined in the present study is negligible in these products. Quality control of the analytical results indicated that the applied NAA procedure is adequate for human nail analysis. (author)

  4. 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

  5. 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

  6. 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.)

  7. Determination of 25 elements in biological standard reference materials by neutron activation analysis

    International Nuclear Information System (INIS)

    Guzzi, G.; Pietra, R.; Sabbioni, E.

    1974-12-01

    Standard and Certified Reference Materials programme of the JRC includes the determination of trace elements in complex biological samples delivered by the U.S. National Bureau of Standards: Bovine liver (NBS SRM 1577), Orchard Leaves (NBS SRM 1571) and Tomato Leaves. The study has been performed by the use of neutron activation analysis. Due to the very low concentration of some elements, radiochemical groups or elemental separation procedures were necessary. The paper describes the techniques used to analyse 25 elements. Computer assisted instrumental neutron activation analysis with high resolution Ge(Li) spectrometry was considerably advantageous in the determination of Na, K, Cl, Mn, Fe, Rb and Co and in some cases of Ca, Zn, Cs, Sc, and Cr. For low contents of Ca, Mg, Ni and Si special chemical separation schemes, followed by Cerenkov counting have been developped. Two other separation procedures allowing the determination of As, Cd, Ga, Hg, Mo, Cu, Sr Se, Ba and P have been set up. The first, the simplified one involves the use of high resolution Ge(Li) detectors, the second, the more complete one involves a larger number of shorter measurements performed by simpler and more sensitive techniques, such as NaI(Tl) scintillation spectrometry and Cerenkov counting. The results obtained are presented and discussed

  8. 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).

  9. ALI and DAC for transuranic elements based on the metabolic data presented in ICRP Publication 48

    International Nuclear Information System (INIS)

    Togawa, Orihiko; Yamaguchi, Yukichi; Homma, Toshimitsu

    1987-07-01

    The recently published ICRP report, ICRP Publication 48, presents the new metabolic data of some transuranic elements, compared with those employed in the calculation of ALI and DAC in ICRP Publication 30. Values of ALI and DAC for 72 radionuclides were calculated using the metabolic data presented in the Publication 48. The calculation was performed by a computer code system DOSDAC, which can systematically calculate ALI and DAC by the same method as that described in the Publication 30. The calculated values of ALI and DAC were tabulated in the same format as that of the supplements to the Publication 30. For the convenience of using in the dose assessment, also given are values of committed effective dose equivalent per intake of unit activity. It is expected that these values will be applied to the radiation protection purposes. (author)

  10. Specificity determinants for the abscisic acid response element ?

    OpenAIRE

    Sarkar, Aditya Kumar; Lahiri, Ansuman

    2013-01-01

    Abscisic acid (ABA) response elements (ABREs) are a group of cis-acting DNA elements that have been identified from promoter analysis of many ABA-regulated genes in plants. We are interested in understanding the mechanism of binding specificity between ABREs and a class of bZIP transcription factors known as ABRE binding factors (ABFs). In this work, we have modeled the homodimeric structure of the bZIP domain of ABRE binding factor 1 from Arabidopsis thaliana (AtABF1) and studied its interac...

  11. 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)

  12. Determination of chilling temperature effects on nutrient elements ...

    African Journals Online (AJOL)

    These seedlings were subsequently, cut into root tip, root middle part, root upper part, hypocotyl, epicotyl, petiole and leaf and sampled randomly. Concentrations of inorganic elements (Al, Si, P, S, Cl, K, Ca, Fe, and Mg) in the parts were measured by wavelength-dispersive X-ray fluorescence (WDXRF) spectrometry to test ...

  13. Determination of toxic elements in tobacco products by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Ahmad, S.; Chaudhry, M.S.; Qureshi, I.H.

    1979-01-01

    The concentration of 15 elements in various brands of cigarette tobacco and cigarette wrapping paper were determined using instrumental neutron activation analysis. The paper of some of the brands contains higher concentrations of toxic elements than the tobacco. The cigarette filter and the ash were also analyzed to determine the adsorption of toxic elements on the filter and their transference in smoke. The toxic effects of some of the elements have been briefly discussed. (author)

  14. 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

  15. X-ray microanalysis of elements present in the matrix of cnidarian nematocysts.

    Science.gov (United States)

    Tardent, P; Zierold, K; Klug, M; Weber, J

    1990-01-01

    The composition and concentration of elements, in particular those of metallic cations, present in the intracapsular matrix and the wall of nematocysts of various cnidarian species have been recorded by means of X-ray microanalysis performed on 100nm thick cryosections. The predominant cation detected in the nematocyst matrix of the hydrozoan Podocoryne carnea (medusa), the scyphozoan Aurelia aurita (scyphopolyp) and the anthozoan Calliactis parasitica (tentacles and acontia) is K(+). Mg(2+) prevails in tentacular cysts of Anthopleura elegantissima, Actinia equina and Anemonia viridis, whereas, the acrorhagial cysts of A. elegantissima and A. equina contain Ca(2+) instead of Mg(2+). The acrorhagial cysts of A. viridis contain Mg(2+) like those of the tentacles. In the tentacular nematocysts of Podocoryne carnea polyps (Hydrozoa) on the other hand ambiguous element contents were found indicating that the cysts of this species has no preference for a particular cation. The high values of sulfur recorded in the matrix and particularly the wall of all the cysts are reflecting the presence of numerous protein disulfide bonds within the structural components (wall, shaft, tubule) of the nematocysts.

  16. 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

  17. Determination of toxic and essential elements in foodstuffs from local market in Jakarta

    International Nuclear Information System (INIS)

    Sadjirun, S.

    1994-01-01

    This report presents data on toxic and essential elements such as As, Cd, Cr, Cu, Hg, Pb, Sb, Se, and Zn in rice, corn, bean, wheat, small green pea, vegetables, fruits, tea, coffee, sea foods, meat, chicken, intestines and associated organs, and eggs as consumed in Jakarta. As, Hg, Sb, Cr, Se, and Zn were determined using instrumental neutron activation analysis (INAA) after being irradiated at TRIGA MARK II reactor, while Cd, Cu, and Pb were determined using atomic absorption spectrometry (AAS). The results obtained were lower than the maximum permissible concentrations allowed. (author). 6 refs, 9 tabs

  18. Analytical Determining Of The Steinmetz Equivalent Diagram Elements Of Single-Phase Transformer

    Directory of Open Access Journals (Sweden)

    T. Aly Saandy

    2015-08-01

    Full Text Available This article presents to an analytical calculation methodology of the Steinmetz Equivalent Diagram Elements applied to the prediction of Eddy current loss in a single-phase transformer. Based on the electrical circuit theory the active and reactive powers consumed by the core are expressed analytically in function of the electromagnetic parameters as resistivity permeability and the geometrical dimensions of the core. The proposed modeling approach is established with the duality parallel series. The equivalent diagram elements empirically determined by Steinmetz are analytically expressed using the expressions of the no loaded transformer consumptions. To verify the relevance of the model validations both by simulations with different powers and measurements were carried out to determine the resistance and reactance of the core. The obtained results are in good agreement with the theoretical approach and the practical results.

  19. 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

  20. 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

  1. EDXRF for determination of chemical elements in the beetle Alphitobius diaperinus

    International Nuclear Information System (INIS)

    Cantinha, Rebeca S.; Farias, Emerson E.G. de; Magalhaes, Marcelo L.R. de; Franca, Elvis J. de; Cunha, Franklin M. da; Zacarias, Vyvyane L.

    2015-01-01

    Energy Dispersion X-Ray Fluorescence (EDXRF) spectrometry has been widely employed for chemical element determination of biological matrices, including insects. The beetle Alphitobius diaperinus is a major problem in poultry production, thereby infesting poultry litter and stored grains. Up to now, little is known about the behavior, physiology and environmental interactions of this insect. In this paper, EDXRF was applied to quantify the main chemical elements in A. diaperinus. For the quality of the analytical protocol, certified reference materials produced by National Institute of Standards and Technology - NIST were analyzed together with the samples. The technique was able to quantify Cl, P, S and Zn in this insect, presenting no significant variation at the 95% confidence level among the repetitions (n = 4). A different pattern of chemical element accumulation in this beetle was noticed compared to other Coleoptera species, in which the concentration of the chemical elements were markedly lower in A. diaperinus, probably associated to the restricted availability of chemical elements in food. Since no result has been found in the literature before, A. diaperinus was firstly chemically characterized in this paper. (author)

  2. EDXRF for determination of chemical elements in the beetle Alphitobius diaperinus

    Energy Technology Data Exchange (ETDEWEB)

    Cantinha, Rebeca S.; Farias, Emerson E.G. de; Magalhaes, Marcelo L.R. de; Franca, Elvis J. de, E-mail: rebecanuclear@gmail.com, E-mail: emersonemiliano@yahoo.com.br, E-mail: marcelo_rlm@hotmail.com, E-mail: ejfranca@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil); Cunha, Franklin M. da; Zacarias, Vyvyane L., E-mail: ukento@yahoo.com.br, E-mail: vyvyanebiologicas@gmail.com [Universidade Federal Rural de Pernambuco (UFRPE), Recife, PE (Brazil)

    2015-07-01

    Energy Dispersion X-Ray Fluorescence (EDXRF) spectrometry has been widely employed for chemical element determination of biological matrices, including insects. The beetle Alphitobius diaperinus is a major problem in poultry production, thereby infesting poultry litter and stored grains. Up to now, little is known about the behavior, physiology and environmental interactions of this insect. In this paper, EDXRF was applied to quantify the main chemical elements in A. diaperinus. For the quality of the analytical protocol, certified reference materials produced by National Institute of Standards and Technology - NIST were analyzed together with the samples. The technique was able to quantify Cl, P, S and Zn in this insect, presenting no significant variation at the 95% confidence level among the repetitions (n = 4). A different pattern of chemical element accumulation in this beetle was noticed compared to other Coleoptera species, in which the concentration of the chemical elements were markedly lower in A. diaperinus, probably associated to the restricted availability of chemical elements in food. Since no result has been found in the literature before, A. diaperinus was firstly chemically characterized in this paper. (author)

  3. Determination of toxic elements in foodstuffs in Vietnam

    International Nuclear Information System (INIS)

    Nguyen Van Minh; Le Thi Ngoc Trinh; Nguyen Giang; Le Tat Mua; Nguyen Mong Sinh

    2006-01-01

    The studying samples of this work have been collected from different areas of Vietnam including industrial areas in HCM city, Dongnai, Vungtau and non-industrial area, Dalat city. The concentrations of the toxic elements as: As, Hg, Cr, Co, Fe, Cu, Cd, Se, As, Zn, Pb in many foodstuff samples together with intercomparison sample which have been distributed by National Food Administration (Sweden) were analyzed by Instrumental Neutron Activation Analysis (INAA), Radiochemical Neutron Activation Analysis (RNAA); Atomic Absorption Spectrophotometer (AAS) and Anodic Stripping Voltammeter (ASV). The obtained results shown that the concentration of toxic elements in the collected samples from selected industrial areas of Vietnam are lower than the maximum permissible concentrations. (author)

  4. 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

  5. Edxrf determination of major and minor elements in compound fertilizers

    DEFF Research Database (Denmark)

    Christensen, Leif Højslet; Rasmussen, Leif W.

    1985-01-01

    The combination of the energy-dispersive x-ray fluorescence technique and a backscatter/fundamental parameter-based matrix correction approach provides a new and unique solution to elemental analyses of fertilizers. This is demonstrated by means of results obtained for three reference materials...... and a range of in-house fertilizers. The results further demonstrate problems of sample preparation as well as the precision and accuracy of the method....

  6. 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

  7. 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

  8. 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

  9. EDXRF applied to the chemical element determination of small invertebrate samples

    International Nuclear Information System (INIS)

    Magalhaes, Marcelo L.R.; Santos, Mariana L.O.; Cantinha, Rebeca S.; Souza, Thomas Marques de; Franca, Elvis J. de

    2015-01-01

    Energy Dispersion X-Ray Fluorescence - EDXRF is a fast analytical technique of easy operation, however demanding reliable analytical curves due to the intrinsic matrix dependence and interference during the analysis. By using biological materials of diverse matrices, multielemental analytical protocols can be implemented and a group of chemical elements could be determined in diverse biological matrices depending on the chemical element concentration. Particularly for invertebrates, EDXRF presents some advantages associated to the possibility of the analysis of small size samples, in which a collimator can be used that directing the incidence of X-rays to a small surface of the analyzed samples. In this work, EDXRF was applied to determine Cl, Fe, P, S and Zn in invertebrate samples using the collimator of 3 mm and 10 mm. For the assessment of the analytical protocol, the SRM 2976 Trace Elements in Mollusk produced and SRM 8415 Whole Egg Powder by the National Institute of Standards and Technology - NIST were also analyzed. After sampling by using pitfall traps, invertebrate were lyophilized, milled and transferred to polyethylene vials covered by XRF polyethylene. Analyses were performed at atmosphere lower than 30 Pa, varying voltage and electric current according to the chemical element to be analyzed. For comparison, Zn in the invertebrate material was also quantified by graphite furnace atomic absorption spectrometry after acid treatment (mixture of nitric acid and hydrogen peroxide) of samples have. Compared to the collimator of 10 mm, the SRM 2976 and SRM 8415 results obtained by the 3 mm collimator agreed well at the 95% confidence level since the E n Number were in the range of -1 and 1. Results from GFAAS were in accordance to the EDXRF values for composite samples. Therefore, determination of some chemical elements by EDXRF can be recommended for very small invertebrate samples (lower than 100 mg) with advantage of preserving the samples. (author)

  10. EDXRF applied to the chemical element determination of small invertebrate samples

    Energy Technology Data Exchange (ETDEWEB)

    Magalhaes, Marcelo L.R.; Santos, Mariana L.O.; Cantinha, Rebeca S.; Souza, Thomas Marques de; Franca, Elvis J. de, E-mail: marcelo_rlm@hotmail.com, E-mail: marianasantos_ufpe@hotmail.com, E-mail: rebecanuclear@gmail.com, E-mail: thomasmarques@live.com.pt, E-mail: ejfranca@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil)

    2015-07-01

    Energy Dispersion X-Ray Fluorescence - EDXRF is a fast analytical technique of easy operation, however demanding reliable analytical curves due to the intrinsic matrix dependence and interference during the analysis. By using biological materials of diverse matrices, multielemental analytical protocols can be implemented and a group of chemical elements could be determined in diverse biological matrices depending on the chemical element concentration. Particularly for invertebrates, EDXRF presents some advantages associated to the possibility of the analysis of small size samples, in which a collimator can be used that directing the incidence of X-rays to a small surface of the analyzed samples. In this work, EDXRF was applied to determine Cl, Fe, P, S and Zn in invertebrate samples using the collimator of 3 mm and 10 mm. For the assessment of the analytical protocol, the SRM 2976 Trace Elements in Mollusk produced and SRM 8415 Whole Egg Powder by the National Institute of Standards and Technology - NIST were also analyzed. After sampling by using pitfall traps, invertebrate were lyophilized, milled and transferred to polyethylene vials covered by XRF polyethylene. Analyses were performed at atmosphere lower than 30 Pa, varying voltage and electric current according to the chemical element to be analyzed. For comparison, Zn in the invertebrate material was also quantified by graphite furnace atomic absorption spectrometry after acid treatment (mixture of nitric acid and hydrogen peroxide) of samples have. Compared to the collimator of 10 mm, the SRM 2976 and SRM 8415 results obtained by the 3 mm collimator agreed well at the 95% confidence level since the E{sub n} Number were in the range of -1 and 1. Results from GFAAS were in accordance to the EDXRF values for composite samples. Therefore, determination of some chemical elements by EDXRF can be recommended for very small invertebrate samples (lower than 100 mg) with advantage of preserving the samples. (author)

  11. A study on chemical element determinations in human nails by neutron activation analysis

    International Nuclear Information System (INIS)

    Sanches, Thalita Pinheiro; Saiki, Mitiko

    2013-01-01

    Nail analyses have been the object of study in order to assess the levels of elements accumulated in the human organism and to use this tissue to monitor environmental and occupational exposure, to evaluate the nutritional status, to verify intoxication by toxic metals and to diagnose or to prevent diseases. Nail analyses present advantages due to easy sample collection, storage, transportation and this tissue provides element level accumulation over time. However, there is controversy regarding the application of nail analysis data due to difficulties to establish reliable reference values or element concentration ranges as control values. The objective of this study was to evaluate the factors that can affect nail element concentrations for further sample analyses of a group of individuals by applying neutron activation analysis (NAA). Fingernails and toenails collected from adult individuals of both genders, aged 18 to 71 years, living in the Sao Paulo Metropolitan Region were cut in small fragments, cleaned and dried for analyses. Samples and element standards were irradiated for 16 h under a thermal neutron flux of about 4.5 x 10 12 n cm -2 s -1 at the IEA-R1 nuclear research reactor followed by gamma ray spectrometry. Element concentrations for As, Br, Ca, Co, Cr, Cs, Fe, K, La, Na, Rb, Sb, Sc, Se and Zn were determined. For quality control of the analytical results, certified reference materials were analysed and the results showed good accuracy and precision with relative errors and relative standard deviations lower than 5.1 % and 11.6 %, respectively. Preliminary assays indicated that the contribution due to impurities from plastic involucres used in the irradiation as well as those from nail polishes is very low and could be considered negligible. Results from the nail sample cleaning process using distinct procedures indicated that HNO 3 solution may cause sample dissolution. Sample homogeneity was verified by analysis of a sample in replicate. A

  12. A study on chemical element determinations in human nails by neutron activation analysis

    International Nuclear Information System (INIS)

    Sanches, Thalita Pinheiro

    2012-01-01

    Nail analyses have been the object of study in order to assess the levels of elements accumulated in the human organism and to use this tissue to monitor environmental and occupational exposure, to evaluate the nutritional status, to verify intoxication by toxic metals and to diagnose or to prevent diseases. Nail analyses present advantages due to easy sample collection, storage, transportation and this tissue provides element level accumulation over time. However, there is controversy regarding the application of nail analysis data due to difficulties to establish reliable reference values or element concentration ranges as control values. The objective of this study was to evaluate the factors that can affect nail element concentrations for further sample analyses of a group of individuals by applying neutron activation analysis (NAA). Fingernails and toenails collected from adult individuals of both genders, aged 18 to 71 years, living in the Sao Paulo Metropolitan Region were cut in small fragments, cleaned and dried for analyses. Samples and element standards were irradiated for 16 h under a thermal neutron flux of about 4.5 x 10 12 n cm -2 s -1 at the IEA-R1 nuclear research reactor followed by gamma ray spectrometry. Element concentrations for As, Br, Ca, Co, Cr, Cs, Fe, K, La, Na, Rb, Sb, Sc, Se and Zn were determined. For quality control of the analytical results, certified reference materials were analysed and the results showed good accuracy and precision with relative errors and relative standard deviations lower than 5.1 % and 11.6 %, respectively. Preliminary assays indicated that the contribution due to impurities from plastic involucres used in the irradiation as well as those from nail polishes is very low and could be considered negligible. Results from the nail sample cleaning process using distinct procedures indicated that HNO 3 solution may cause sample dissolution. Sample homogeneity was verified by analysis of a sample in replicate. A

  13. A study on chemical element determinations in human nails by neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Sanches, Thalita Pinheiro; Saiki, Mitiko, E-mail: thalitapsanches@usp.br, E-mail: mitiko@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    Nail analyses have been the object of study in order to assess the levels of elements accumulated in the human organism and to use this tissue to monitor environmental and occupational exposure, to evaluate the nutritional status, to verify intoxication by toxic metals and to diagnose or to prevent diseases. Nail analyses present advantages due to easy sample collection, storage, transportation and this tissue provides element level accumulation over time. However, there is controversy regarding the application of nail analysis data due to difficulties to establish reliable reference values or element concentration ranges as control values. The objective of this study was to evaluate the factors that can affect nail element concentrations for further sample analyses of a group of individuals by applying neutron activation analysis (NAA). Fingernails and toenails collected from adult individuals of both genders, aged 18 to 71 years, living in the Sao Paulo Metropolitan Region were cut in small fragments, cleaned and dried for analyses. Samples and element standards were irradiated for 16 h under a thermal neutron flux of about 4.5 x 10{sup 12} n cm{sup -2} s{sup -1} at the IEA-R1 nuclear research reactor followed by gamma ray spectrometry. Element concentrations for As, Br, Ca, Co, Cr, Cs, Fe, K, La, Na, Rb, Sb, Sc, Se and Zn were determined. For quality control of the analytical results, certified reference materials were analysed and the results showed good accuracy and precision with relative errors and relative standard deviations lower than 5.1 % and 11.6 %, respectively. Preliminary assays indicated that the contribution due to impurities from plastic involucres used in the irradiation as well as those from nail polishes is very low and could be considered negligible. Results from the nail sample cleaning process using distinct procedures indicated that HNO{sub 3} solution may cause sample dissolution. Sample homogeneity was verified by analysis of a sample in

  14. Multielement determination of rare earth elements by liquid chromatography/inductively coupled plasma atomic emission spectrometry

    International Nuclear Information System (INIS)

    Sawatari, Hideyuki; Asano, Takaaki; Hu, Xincheng; Saizuka, Tomoo; Itoh, Akihide; Hirose, Akio; Haraguchi, Hiroki

    1995-01-01

    The rapid determination of rare earth elements (REEs) has been investigated by an on-line system of high performance liquid chromatography/multichannel inductively coupled plasma atomic emission spectrometry. In the present system, all REEs could be detected simultaneously in a single chromatographic measurement without spectral interferences. Utilizing a cation exchange column and 2-hydroxy-2-methylpropanoic acid aqueous solution as the mobile phase, the detection limits of 0.4-30 ng ml -1 for all REEs were obtained. The system was applied to the determination of REEs in geological standard rock samples and rare earth impurities in high purity rare earth oxides. The REEs in standard rocks could be determined by the present HPLC/ICP-AES system without pretreatment after acid digestion, although the detection limits were not sufficient for the analysis of rare earth oxides. (author)

  15. Magnesium analysis. Determination of 5 elements by impulse polarography

    International Nuclear Information System (INIS)

    Anon.

    Determination of cadmium, copper, nickel, lead and zinc in magnesium used in magnesiothermics. The process is as follow: magnesium dissolution in hydrochloric acid, neutralisation by ammonia, addition of ammonium chloride and citric acid, ammonia is added until pH8. Addition of pyridine, polarographic determination of zinc and then of cadmium and copper [fr

  16. The use of magnetic Barkhausen noise analysis for nondestructive determination of stresses in structural elements

    International Nuclear Information System (INIS)

    Silva Junior, Silverio Ferreira da; Mansur, Tanius Rodrigues; Cruz, Julio Ricardo Barreto

    2007-01-01

    The knowledge about the stress state acting in structural elements has significant importance in the structural integrity evaluation of a specific component. The magnetic Barkhausen noise analysis can be used for this purpose. As a nondestructive testing method, it presents the advantage of not promote any changes in the tested component. In this paper, a study about the use of this new nondestructive test method for stress measurements is presented. The test system configuration and the reference standards used for this purpose, as well as the optimum test parameters determination are discussed. The experiments were carried out in ASTM A-36 steel, used for structural components manufacturing. A structure of this material was loaded and the resulting stresses were determined from strain gage measurements and Barkhausen noise analysis. The results obtained have showed a good sensitivity of the magnetic Barkhausen noise to stress changes occurred in the material. The main advantages and limitations of this test method for stress measurements are presented. (author)

  17. Determination of acoustic vibration in watermelon by finite element modeling

    Science.gov (United States)

    Nourain, Jamal; Ying, Yibin B.; Wang, Jianping; Rao, Xiuqin

    2004-11-01

    The analysis of the vibration responses of a fruit is suggested to measure firmness non-destructively. A wooden ball excited the fruits and the response signals were captured using an accelerometer sensor. The method has been well studied and understood on ellipsoidal shaped fruit (watermelon). In this work, using the finite element simulations, the applicability of the method on watermelon was investigated. The firmness index is dependent on the mass, density, and natural frequency of the lowest spherical modes (under free boundary conditions). This developed index extends the firmness estimation for fruits or vegetables from a spherical to an ellipsoidal shape. The mode of Finite element analysis (FEA) of watermelon was generated based on measured geometry, and it can be served as a theoretical reference for predicting the modal characteristics as a function of design parameters such as material, geometrical, and physical properties. It was found that there were four types of mode shapes. The 1st one was first-type longitudinal mode, the 2nd one was the second-type longitudinal mode, the 3rd one was breathing mode or pure compression mode, and the fourth was flexural or torsional mode shape. As suggested in many references, the First-type spherical vibration mode or oblate-Prolate for watermelon is the lowest bending modes, it's most likely related to fruit firmness. Comparisons of finite element and experimental modal parameters show that both results were agreed in mode shape as well as natural frequencies. In order to measure the vibration signal of the mode, excitation and sensors should be placed on the watermelon surface far away from the nodal lines. The excitation and the response sensors should be in accordance with vibration directions. The correlations between the natural frequency and firmness was 0.856, natural frequency and Young's modulus was 0.800, and the natural frequency and stiffness factor (SF) was 0.862. The stiffness factor (SF) is adequate

  18. 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.

  19. Water analysis. Determination of elements by atomic absorption

    International Nuclear Information System (INIS)

    Anon.

    Analysis of homogeneous water solutions (plain water, polluted waters, effluents...) by atomic absorption spectrometry with correction for non specific absorption. The quantity ratio is determined by comparison with standard solutions, correction tables are given [fr

  20. Determining Trajectory of Triboelectrically Charged Particles, Using Discrete Element Modeling

    Science.gov (United States)

    2008-01-01

    The Kennedy Space Center (KSC) Electrostatics and Surface Physics Laboratory is participating in an Innovative Partnership Program (IPP) project with an industry partner to modify a commercial off-the-shelf simulation software product to treat the electrodynamics of particulate systems. Discrete element modeling (DEM) is a numerical technique that can track the dynamics of particle systems. This technique, which was introduced in 1979 for analysis of rock mechanics, was recently refined to include the contact force interaction of particles with arbitrary surfaces and moving machinery. In our work, we endeavor to incorporate electrostatic forces into the DEM calculations to enhance the fidelity of the software and its applicability to (1) particle processes, such as electrophotography, that are greatly affected by electrostatic forces, (2) grain and dust transport, and (3) the study of lunar and Martian regoliths.

  1. HuR binding to AU-rich elements present in the 3' untranslated region of Classical swine fever virus

    Directory of Open Access Journals (Sweden)

    Huang Chin-Cheng

    2011-07-01

    Full Text Available Abstract Background Classical swine fever virus (CSFV is the member of the genus Pestivirus under the family Flaviviridae. The 5' untranslated region (UTR of CSFV contains the IRES, which is a highly structured element that recruits the translation machinery. The 3' UTR is usually the recognition site of the viral replicase to initiate minus-strand RNA synthesis. Adenosine-uridine rich elements (ARE are instability determinants present in the 3' UTR of short-lived mRNAs. However, the presence of AREs in the 3' UTR of CSFV conserved in all known strains has never been reported. This study inspects a possible role of the ARE in the 3' UTR of CSFV. Results Using RNA pull-down and LC/MS/MS assays, this study identified at least 32 possible host factors derived from the cytoplasmic extracts of PK-15 cells that bind to the CSFV 3' UTR, one of which is HuR. HuR is known to bind the AREs and protect the mRNA from degradation. Using recombinant GST-HuR, this study demonstrates that HuR binds to the ARE present in the 3' UTR of CSFV in vitro and that the binding ability is conserved in strains irrespective of virulence. Conclusions This study identified one of the CSFV 3' UTR binding proteins HuR is specifically binding to in the ARE region.

  2. 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

  3. 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.

  4. 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

  5. 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)

  6. 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.

  7. 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

  8. Determination of rare earth elements in red mud by ICP-MS

    International Nuclear Information System (INIS)

    Kumar, Sanjukta A.; Suvarna, S.; Kiran Kumar, G.

    2017-01-01

    Red mud or red sludge is a highly alkaline waste product composed mainly of iron oxide that is generated in the industrial production of aluminum from bauxite. With about 77 million tons of this hazardous material being produced annually, red mud poses a serious disposal problem in the mining industry. Discharge of red mud is hazardous environmentally because of its alkalinity. Many studies have been conducted to develop uses of red mud. An estimated 2 to 3 million tones are used annually in the production of cement, road construction and as a source for iron. Potential applications include the production of low cost concrete, application to sandy soils to improve phosphorus cycling, amelioration of soil acidity, landfill capping and carbon sequestration. Red mud contains a large amount of iron along with appreciable concentrations of many strategic elements such as rare earth elements and therefore can be a source of valuable secondary raw material. This necessitates the elemental characterization of red mud. This paper presents an effective dissolution procedure using a mixture of phosphoric acid and nitric acid for red mud followed by determination of rare earth elements by ICP-MS. The method was validated by spike recovery experiments. The recoveries were found within 98 to 102 %. The relative standard deviation (RSD) of the method was found to be within 5 %

  9. X-ray spectrum determination of elements with low atomic number with use of electron microscope

    International Nuclear Information System (INIS)

    Smirnov, V.N.

    1982-01-01

    Separate assemblies of a commercial analytical electron microscope-microanalyzer EMMA-2 have been modified to study objects, containing elements with the atomic number Z=5-9, in particular: 1) the range of changing the accelerating voltages is expanded to be in the range of 25 down to 10 kV with 5 kV interval. 2) image intensifier using microchannel plate MKP-40-19 is applied; 3) for elements of carbon, oxygen, boron, nitrogen type a unit with flow-type proportional counter is used. The sensitivity of carbon- and oxygen determination in carbides and oxides is 0.15-0.3% at the measurement time of 100 s. Results of microanalysis of the particles of B 2 O 3 , Al 2 O 3 , SiO 2 , Fe 2 O 3 , Fe 3 C, WC for the contents of oxygen and carbon are presented

  10. Determination of reference values of elements in kidney of the wistar rats using NAA

    International Nuclear Information System (INIS)

    Oliveira, Laura C.; Zamboni, Cibele B.

    2013-01-01

    The aim of the present study is to establish Reference Value for elements in kidney of Wistar rats using the Neutron Activation Analysis technique. The quantitative knowledge of these elements in this biological material allows researchers to optimize their studies, both in terms of cost and time, selecting the species that fits to the experimental model as a clinical reference, as well as the realization of biochemical investigation in kidney. In this study, the reference values (mg/kg) for kidney were determined for: Cr (0.0276 - 0.0384), Fe (110.23 - 212.87), Rb (2.8 - 6.8) and Zn (78.40 - 84.56). (author)

  11. Determination of elemental levels in radiopharmaceuticals by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Capote Rodriguez, Gil; Guevara, Sergio Ribeiro; Arribere, Maria; Hernandez Rivero, Tulio

    2001-01-01

    Neutron Activation Analysis (NAA) both Instrumental (INAA) and Radiochemical (RNAA) have been extensively applied to the determination of minor and trace elements in samples of quite different origin and composition. Particularly, the analysis of microquantities of toxic elements in biological samples by INAA and RNAA is extensively reported. NAA has been also applied to the determination of minor and trace constituents in biomedical products. The use of the INAA in pharmaceutical samples has not been reported yet. This could be due in some extent because of the specificity of these types of samples, and also because of the need to irradiate the samples in a nuclear reactor. The objective of the present work was to study the feasibility of applying INAA for the quantification of minor and trace constituents in three radiopharmaceuticals. The formulation of these products was elaborated by the Isotope Center and proposed for registration to the corresponding authorities. The active components of three radiopharmaceuticals were analyzed: Hexamethylene propylene Amino oxine (HMPAO), Dimercaptosuccinic Acid (DMSA) and Diethylenetriamine penta-acetic Acid (DTPA). The samples were dried up to constant weight at room temperature. In order to avoid possible interferences from the irradiated polyethylene vials, the samples were pressed into the form of pills using a die of stainless steel. The weights of the samples ranged from 50 mg to 200 mg. Samples in duplicates were irradiated in the 0.5 k W Bariloche RA-6 Research Nuclear Reactor. To induce more (n,gamma) reactions and therefore increase the number of analytes and also to minimize interferences from activation products, the irradiation was carried out using two regimens. For the measurement, irradiated pills were put into clean polyethylene containers. The measurements were carried out with a 67 cm 3 ORTEC HPGe intrinsic-N coaxial detector with a resolution of 2.0 keV FWHM at 1.33 MeV and with an efficiency of 12

  12. Determination of rare earth elements in tomato plants by inductively coupled plasma mass spectrometry techniques.

    Science.gov (United States)

    Spalla, S; Baffi, C; Barbante, C; Turetta, C; Turretta, C; Cozzi, G; Beone, G M; Bettinelli, M

    2009-10-30

    In recent years identification of the geographical origin of food has grown more important as consumers have become interested in knowing the provenance of the food that they purchase and eat. Certification schemes and labels have thus been developed to protect consumers and genuine producers from the improper use of popular brand names or renowned geographical origins. As the tomato is one of the major components of what is considered to be the healthy Mediterranean diet, it is important to be able to determine the geographical origin of tomatoes and tomato-based products such as tomato sauce. The aim of this work is to develop an analytical method to determine rare earth elements (RRE) for the control of the geographic origin of tomatoes. The content of REE in tomato plant samples collected from an agricultural area in Piacenza, Italy, was determined, using four different digestion procedures with and without HF. Microwave dissolution with HNO3 + H2O2 proved to be the most suitable digestion procedure. Inductively coupled plasma quadrupole mass spectrometry (ICPQMS) and inductively coupled plasma sector field plasma mass spectrometry (ICPSFMS) instruments, both coupled with a desolvation system, were used to determine the REE in tomato plants in two different laboratories. A matched calibration curve method was used for the quantification of the analytes. The detection limits (MDLs) of the method ranged from 0.03 ng g(-1) for Ho, Tm, and Lu to 2 ng g(-1) for La and Ce. The precision, in terms of relative standard deviation on six replicates, was good, with values ranging, on average, from 6.0% for LREE (light rare earth elements) to 16.5% for HREE (heavy rare earth elements). These detection limits allowed the determination of the very low concentrations of REE present in tomato berries. For the concentrations of REE in tomato plants, the following trend was observed: roots > leaves > stems > berries. Copyright 2009 John Wiley & Sons, Ltd.

  13. B lymphocytes as natural antigen-presenting cells (APC) of their own Ig receptor determinants

    International Nuclear Information System (INIS)

    Yurin, V.L.; Rudensky, A.Yu.; Rabinovich, O.R.; Kulakova, O.G.; Bobreneva, R.A.

    1986-01-01

    The authors use Igk-lb allotype-specific rat T cell proliferation(Pr) in vitro as a model of natural Ig determinants B cell presentation in Ig-specific T-B cell interactions. As shown before Igk-lb-specific responsiveness of AUG(RT-l/sup c/, Igk-la) and WAG (RT-l, Igk-la) rats is controlled by dominant Ir gene, linked to RT-l/sup c/. Only IgG(Igk-lb)-pulsed splenic APC of AUG(responder) but not WAG(non-responder) origin induce specific F 1 (WAGxAUG) T cell Pr. The same restriction was observed if purified B cells from Igk-l congeneic AUG-lb and WAG-lb rats were used as APC. B cell presentation was found to be sensitive to high irradiation dose(2000 rad). Anti-RT-l monoclonal antibody inhibition studies suggested RT-lB(I-A) molecule as a main restricting element of Igk-lb T cell recognition. B cell and splenic APC presentation of Igk-lb allotype was not inhibited by poly- and monoclonal anti-Igk-lb antibodies. Allelic exclusion of Igk-lb presentation by B cells from heterozygous F 1 (WAG-lbx AUG) rats was demonstrated by panning with antiallotypic reagents. Important, that irradiated anti-Igk-lb T cells induce specific Pr of normal Igk-lb-positive B cells. The data demonstrate MHC-restricted B cell presentation of their own receptor determinants, distinct from serologically-defined epitopes. T cell recognition of these determinants induce specific Pr of Ig-recognizing T cells and Ig-presenting B lymphocytes

  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. Preliminary study on element mass fraction determination on catfish samples from Paraguay

    International Nuclear Information System (INIS)

    Moreira, Edson G.; Catharino, Marilia G.M.; Vasconcellos, Marina B.A.; Frutos, Sixto A.; Insaurralde, Mario S.

    2013-01-01

    South American catfish (Pseudoplatystoma), commonly known in Spanish as atigrado or surubi and in Portuguese as surubim or pintado is a large fish that typically reaches 1 m long and weighs 60 kg to 80 kg and may be found at the basins of the Amazon, the Sao Francisco and de la Plata rivers, usually in riverbeds and deep wells. Being a much appreciated fish for human consumption, it is quite sought after by fishermen who have been contributing to the reduction of the stocks. This fact attracted the attention of the Paraguayan authorities to the point of imposing restrictions to free fishing and commercialization. This study aims to assist the conservation efforts towards this fish by investigating its exposure to possible pollutants. Preliminary results on element determination on six samples of catfish from Paraguayan rivers are presented. Cs, Co, Fe, Se and Zn were determined by applying an Instrumental Neutron Activation Analysis method. While these element levels were lower than the legislation for human consumption, the elements As, Cr e La were not detected in the samples as they are below the detection limit of the method employed. Atomic Absorption Spectrometry was used to investigate the presence of Cd, Hg and Pb in the samples. Hg was detected in the samples while Cd and Pb were below the detection limit of the method. (author)

  16. 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

  17. Preliminary study on element mass fraction determination on catfish samples from Paraguay

    Energy Technology Data Exchange (ETDEWEB)

    Moreira, Edson G.; Catharino, Marilia G.M.; Vasconcellos, Marina B.A., E-mail: emoreira@ipen.br, E-mail: mbvascon@ipen.br, E-mail: mariliasemmler@uol.com.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Frutos, Sixto A.; Insaurralde, Mario S., E-mail: tony8013@hotmail.com, E-mail: insaurraldemar9@hotmail.com [Universidad Nacional de Asuncion (FCV/UNA), San Lorenzo (Paraguay). Facultad de Ciencias Veterinarias. Departamento de Pesca y Acuicultura

    2013-07-01

    South American catfish (Pseudoplatystoma), commonly known in Spanish as atigrado or surubi and in Portuguese as surubim or pintado is a large fish that typically reaches 1 m long and weighs 60 kg to 80 kg and may be found at the basins of the Amazon, the Sao Francisco and de la Plata rivers, usually in riverbeds and deep wells. Being a much appreciated fish for human consumption, it is quite sought after by fishermen who have been contributing to the reduction of the stocks. This fact attracted the attention of the Paraguayan authorities to the point of imposing restrictions to free fishing and commercialization. This study aims to assist the conservation efforts towards this fish by investigating its exposure to possible pollutants. Preliminary results on element determination on six samples of catfish from Paraguayan rivers are presented. Cs, Co, Fe, Se and Zn were determined by applying an Instrumental Neutron Activation Analysis method. While these element levels were lower than the legislation for human consumption, the elements As, Cr e La were not detected in the samples as they are below the detection limit of the method employed. Atomic Absorption Spectrometry was used to investigate the presence of Cd, Hg and Pb in the samples. Hg was detected in the samples while Cd and Pb were below the detection limit of the method. (author)

  18. Device for determining element contents of lignite mass flows by activation analysis

    International Nuclear Information System (INIS)

    Goeldner, R.; Maul, E.; Rose, W.; Wagner, D.

    1987-01-01

    A simple device is presented, apt for continuous operation, to determine the element contents of bulk goods of flowable materials with a suitable granularity, in particular of lignite mass flows to assess the coal quality. Several kilograms of samples can be reproducibly dosed and homogeneously activated by a device consisting of a shielding container with activation chamber and radiation source, a measuring unit with detectors, and a source container, and characterized by a blade wheel in the activation chamber which causes the dosing and homogeneous activation of the sample

  19. Determination of Rare Earth Elements in plants by neutron activation analysis

    International Nuclear Information System (INIS)

    Figueiredo, Ana M.G.; Maria, Sheila P.; Ceccantini, Gregorio C.T.

    1996-01-01

    In the present work, instrumental neutron activation analysis was employed to the determination of rare earth elements (La, Ce, Nd, Eu, Tb, Yb e Lu) in plants, aiming biogeochemical studies. The precision and accuracy of the method were verified by the analysis of the reference materials Citrus Leaves (NIST 1572) and Pine Needles (NIST 1575). With exception of terbium, the results obtained agreed with reference values, giving relative errors less than 25%. The method was applied to different species of plants growing in the alkaline-ultramafic complex of Salitre, MG and the obtained data were compared to the average content in plants. (author)

  20. Bio indicator organisms available to use for determination of radioactive elements in Turkey's seas

    International Nuclear Information System (INIS)

    Kocbas, F.; Guener, H.

    2006-01-01

    In determination of radioactive concentration and monitoring alive and lifeless environmental samples possess a significant place. Thus, intense study is carried out related to natural and artificial radionuclides sediment. Bio indicator living organisms inhabiting in sea ecosystems; are being evaluated in researches such as determinations of environmental pollution, natural and artificial radioactive elements. Turkey's seas are rich related to diversification of various types. In determining and monitoring radioactivity concentration widespread implementation of some sorts appeal attention and on the other hand inadequate usage of many types is observed. In the present study, providing information about the bio indicator organisms keep living in seas and plays important role in food supply chain and increasing the numbers of the types of organisms used are aimed

  1. 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

  2. Strain-Based Damage Determination Using Finite Element Analysis for Structural Health Management

    Science.gov (United States)

    Hochhalter, Jacob D.; Krishnamurthy, Thiagaraja; Aguilo, Miguel A.

    2016-01-01

    A damage determination method is presented that relies on in-service strain sensor measurements. The method employs a gradient-based optimization procedure combined with the finite element method for solution to the forward problem. It is demonstrated that strains, measured at a limited number of sensors, can be used to accurately determine the location, size, and orientation of damage. Numerical examples are presented to demonstrate the general procedure. This work is motivated by the need to provide structural health management systems with a real-time damage characterization. The damage cases investigated herein are characteristic of point-source damage, which can attain critical size during flight. The procedure described can be used to provide prognosis tools with the current damage configuration.

  3. 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.

  4. 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)

  5. Determination of the rare earth elements in marine pore waters and associated sediments

    International Nuclear Information System (INIS)

    Kennedy, H.; Elderfield, H.

    Accurate and precise determinations of natural levels of rare earth elements (R.E.E.) in sea water and pore water are highly reliant upon the size and variability of the analytical blank, the method for determining the yield, and, to a lesser extent, the inherent precision of the instrument used. Isotope dilution mass spectrometry (IDMS) together with ultra-clean room techniques has been successfully used in the determinations of rare earth elements in pore waters. Simultaneous multi-element analysis by inductively coupled plasma atomic emission spectrometry (ICP) provides an alternative to IDMS for a rapid determination of R.E.E. in sediments. (author)

  6. 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)

  7. 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.

  8. 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

  9. Determination of Hf, Sc and Y in geological samples together with the rare-earth elements

    International Nuclear Information System (INIS)

    Lihareva, N.; Delaloye, M.

    1997-01-01

    A method is described for the determination of Hf, Sc and Y simultaneously with the REE in geological materials. An earlier method for REE separation from major elements was studied with the aim to apply it also to the determination of Hf, Sc and Y. Sample decomposition was carried out by melting with LiBO 2 . The method involves separation and concentration stages, using the cation-exchange resin DOWEX AG 50W-X8. Matrix elements were eluted with 2 mol/l HCl, whereas 6 mol/l HNO 3 with oxalic acid and 8 mol/l HNO 3 were used to elute the elements to be determined. Some of the matrix elements could not be completely removed. This effect as well as the recovery rates of the determined elements were investigated. The measurements were performed by ICP-AES. Spectral interferences were also tested. (orig.). With 1 tab

  10. Trace elements determination in tungsten ores by neutron activation analysis

    International Nuclear Information System (INIS)

    Mireles Garcia, F.

    1991-01-01

    The kinetics approach of the leaching of industrial scheelite (CaWO 4 ) concentrates in hydrochloric acid media investigated under controlled acid concentration in leachates, reaction atmospheres and temperature conditions. Experiments show that the scheelite decomposition rate increases as the acid concentration in the leaching solution and temperature increase. The apparent activation energy for the scheelite acid decomposition process is estimated in the present study to be equal to 10.43 Kcal(mol) -1 . On the basis of the experimental results, it is proposed an equilibria competition mechanism as a function of the acid concentration which explains the peculiar behavior of the experimental systems at low temperatures. (Author)

  11. Presentations

    International Nuclear Information System (INIS)

    2007-01-01

    The presented materials consist of presentations of international workshop which held in Warsaw from 4 to 5 October 2007. Main subject of the meeting was progress in manufacturing as well as research program development for neutron detector which is planned to be placed at GANIL laboratory and will be used in nuclear spectroscopy research

  12. 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.

  13. 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)

  14. Sociogeographical elements and determinants of Croatian Islands classification

    Directory of Open Access Journals (Sweden)

    Veni Marinković

    2016-01-01

    Full Text Available Although Croatian Islands belong to the same macro-region of the Adriatic Croatia, they are characterized by a great heterogeneity of their geospatial reality at regional, micro regional, interinsular and local level, as well as by the complexity of the socio-economic structure and dynamic characteristics, as a result of physical-geographical and historical processes and contemporary development trends on them. The paper deals with sociogeographical classification of Croatian archipelago and provides an overview and systematization of scientific and professional considerations of its geospatial heterogeneity. It also includes an overview of Croatian Islands typification based on multi-criteria indicators. The author concluded the work by presenting a proposal of Croatian Islands clusterization concept as a contribution to the islands developmental policy.

  15. 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)

  16. 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)

  17. Zaba: a novel miniature transposable element present in genomes of legume plants

    Czech Academy of Sciences Publication Activity Database

    Macas, Jiří; Neumann, Pavel; Požárková, Dana

    2003-01-01

    Roč. 269, - (2003), s. 624-631 ISSN 1617-4615 R&D Projects: GA ČR GA521/00/0655 Institutional research plan: CEZ:AV0Z5051902 Keywords : DNA * transposable elements * ZABA Subject RIV: EB - Genetics ; Molecular Biology Impact factor: 2.240, year: 2003

  18. Ufo-element presentation in metamodel structure of triune continuum paradigm

    OpenAIRE

    Ukrayinets, ?.

    2006-01-01

    This paper describes results of UFO-element formal description in metamodel structure of Triune Continuum Paradigm. This can promote the solution of a problem of development of methods of mutual system-object UFO- and UML-models transformation for providing of more effective information systems designing, in particular, for visual modelling CASE-tools Rational Rose and UFO-Toolkit integration.

  19. 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

  20. 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

  1. 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.

  2. 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)

  3. 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

  4. Determination of the burn-up of TRIGA fuel elements by calculation with new TRIGLAV program

    International Nuclear Information System (INIS)

    Zagar, T.; Ravnik, M.

    1996-01-01

    The results of fuel element burn-up calculations with new TRIGLAV program are presented. TRIGLAV program uses two dimensional model. Results of calculation are compared to results calculated with program, which uses one dimensional model. The results of fuel element burn-up measurements with reactivity method are presented and compared with the calculated results. (author)

  5. Determination of Elements in Normal and Leukemic Human Whole Blood by Neutron Activation Analysis

    Energy Technology Data Exchange (ETDEWEB)

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

    1961-11-15

    By means of gamma-spectrometry the following elements were simultaneously determined in normal and leukemic human whole blood: Cu, Mn, Zn, Sr, Na, P, Ca, Rb, Cd, Sb, Au, Cs and Fe. Chemical separations were performed according to a group separation method using ion-exchange technique. No significant difference between the concentrations of the elements in normal- and leukemic blood was observed.

  6. Standard recommended practice for examination of fuel element cladding including the determination of the mechanical properties

    International Nuclear Information System (INIS)

    Anon.

    1975-01-01

    Guidelines are provided for the post-irradiation examination of fuel cladding and to achieve better correlation and interpretation of the data in the field of radiation effects. The recommended practice is applicable to metal cladding of all types of fuel elements. The tests cited are suitable for determining mechanical properties of the fuel elements cladding. Various ASTM standards and test methods are cited

  7. Determination of rare earth elements in aluminum by inductively coupled plasma-atomic emission spectroscopy

    International Nuclear Information System (INIS)

    Mahanti, H.S.; Barnes, R.M.

    1983-01-01

    Inductively coupled plasma-atomic emission spectroscopy is evaluated for the determination of 14 rare earth elements in aluminum. Spectral line interference, limit of detection, and background equivalent concentration values are evaluated, and quantitative recovery is obtained from aluminum samples spiked with rare earth elements. The procedure is simple and suitable for routine process control analysis. 20 references, 5 tables

  8. 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)

  9. Determination of Elements in Normal and Leukemic Human Whole Blood by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Brune, D.; Frykberg, B.; Samsahl, K.; Wester, P.O.

    1961-11-01

    By means of gamma-spectrometry the following elements were simultaneously determined in normal and leukemic human whole blood: Cu, Mn, Zn, Sr, Na, P, Ca, Rb, Cd, Sb, Au, Cs and Fe. Chemical separations were performed according to a group separation method using ion-exchange technique. No significant difference between the concentrations of the elements in normal- and leukemic blood was observed

  10. 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

  11. Geochemical landscapes of the conterminous United States; new map presentations for 22 elements

    Science.gov (United States)

    Gustavsson, N.; Bolviken, B.; Smith, D.B.; Severson, R.C.

    2001-01-01

    Geochemical maps of the conterminous United States have been prepared for seven major elements (Al, Ca, Fe, K, Mg, Na, and Ti) and 15 trace elements (As, Ba, Cr, Cu, Hg, Li, Mn, Ni, Pb, Se, Sr, V, Y, Zn, and Zr). The maps are based on an ultra low-density geochemical survey consisting of 1,323 samples of soils and other surficial materials collected from approximately 1960-1975. The data were published by Boerngen and Shacklette (1981) and black-and-white point-symbol geochemical maps were published by Shacklette and Boerngen (1984). The data have been reprocessed using weighted-median and Bootstrap procedures for interpolation and smoothing.

  12. Elemental composition of the particulate matter present in the atmospheric aerosols of Sete Lagoas, MG

    International Nuclear Information System (INIS)

    Queiroz, Paula Guimaraes Moura; Jacomino, Vanusa Maria Feliciano; Menezes, Maria Angela de Barros Correia

    2007-01-01

    The main objective of this study was the identification of sources generating particulate matter in the atmospheric aerosols of Sete Lagoas, Minas Gerais. The measurement of the mineral composition was accomplished by X-ray diffractometry and the elemental concentration by neutron activation analysis. The results showed that Al, Cl, Cu, Fe, K, Mg and Na are the predominant chemical elements in the total suspended particles (TPS). The presence of Na, Ba, Cl, Cu, Eu, Fe and Sm in those particles with aerodynamic diameter smaller than 10 μm (PM 10 ), indicates that soil dust and ceramic and pig iron industries are the main sources of air quality degradation in the region. (author)

  13. Studies on determination of stable elements in sea water and organisms

    International Nuclear Information System (INIS)

    Anon.

    1974-01-01

    The existing conditions of stable elements including Co, Zn, Cs, Ce and Eu in sea water were determined by adding radioactive tracers, and determination methods were discussed. 60 Co added to sea water revealed to be kept in solution in 93 per cent of non-filtrated sea water, and in 98 per cent of filtrated sea water. 65 Zn also added to sea water showed to be kept in solution in 97 per cent of both non-filtrated and filtrated sea water. Both elements seemed to exist as particle or ion smaller than 0.45 μ, which solved in sea water. On the other hand, in both Ce and Eu of rare earth elements, about 80 per cent of them presented in the residue, but the treatment of sea water by hydrochroric acid solubilized 80 to 90 per cent of them in filtrated sea water. One of the instrumental analysis, irradiation analysis by nuclear reactor, was applied: each of preconcentration procedure by ion exchange method for Co and Zn in sea water and drying up sample marine organisms to ash content combined with irradiation analysis. Chemical recovery of both 60 Co and 65 Zn in sea water by preconcentration procedure reached more than 95 per cent. As to marine organisms, Co, Zn, and Cs could be determined with only 100 to 200 mg. of ash content obtained from sample marine organisms showing 80 per cent of chemical yield of the carrier through whole the procedure of analysis in almost all the samples. The chemical recovery of Ce and Eu in sea water and marine organisms by the preconcentration procedure reached about 85 per cent, and chemical yield through whole the procedure of analysis was more than 60 per cent. Concentration factor of Co and Zn in fishes and shells, especially that of muscles, obtained by stable elements determination method was almost 10 times that by RI tracer method. The difference of chemical forms between RI tracer and stable isotope affected not only to physiological metabolism but also to food chains. (Kanao, K.)

  14. Fast sequential multi-element determination of major and minor elements in environmental samples and drinking waters by high-resolution continuum source flame atomic absorption spectrometry.

    Science.gov (United States)

    Gómez-Nieto, Beatriz; Gismera, Ma Jesús; Sevilla, Ma Teresa; Procopio, Jesús R

    2015-01-07

    The fast sequential multi-element determination of 11 elements present at different concentration levels in environmental samples and drinking waters has been investigated using high-resolution continuum source flame atomic absorption spectrometry. The main lines for Cu (324.754 nm), Zn (213.857 nm), Cd (228.802 nm), Ni (232.003 nm) and Pb (217.001 nm), main and secondary absorption lines for Mn (279.482 and 279.827 nm), Fe (248.327, 248.514 and 302.064 nm) and Ca (422.673 and 239.856 nm), secondary lines with different sensitivities for Na (589.592 and 330.237 nm) and K (769.897 and 404.414 nm) and a secondary line for Mg (202.582 nm) have been chosen to perform the analysis. A flow injection system has been used for sample introduction so sample consumption has been reduced up to less than 1 mL per element, measured in triplicate. Furthermore, the use of multiplets for Fe and the side pixel registration approach for Mg have been studied in order to reduce sensitivity and extend the linear working range. The figures of merit have been calculated and the proposed method was applied to determine these elements in a pine needles reference material (SRM 1575a), drinking and natural waters and soil extracts. Recoveries of analytes added at different concentration levels to water samples and extracts of soils were within 88-115% interval. In this way, the fast sequential multi-element determination of major and minor elements can be carried out, in triplicate, with successful results without requiring additional dilutions of samples or several different strategies for sample preparation using about 8-9 mL of sample. Copyright © 2014 Elsevier B.V. All rights reserved.

  15. Presentations

    International Nuclear Information System (INIS)

    2007-01-01

    The PARIS meeting held in Cracow, Poland from 14 to 15 May 2007. The main subjects discussed during this meeting were the status of international project dedicated to gamma spectroscopy research. The scientific research program includes investigations of giant dipole resonance, probe of hot nuclei induced in heavy reactions, Jacobi shape transitions, isospin mixing and nuclear multifragmentation. The mentioned programme needs Rand D development such as new scintillations materials as lanthanum chlorides and bromides as well as new photo detection sensors as avalanche photodiodes - such subjects are also subjects of discussion. Additionally results of computerized simulations of scintillation detectors properties by means of GEANT- 4 code are presented

  16. 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)

  17. 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.)

  18. Determination of toxic elements in tobacco by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Yaprak, G.; Cam, N.F.

    1998-01-01

    The concentration of toxic elements in the tobacco of six different brands of domestic and two brands of imported cigarettes heavily smoked in Turkey were determined using instrumental neutron activation analysis (INAA)

  19. 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)

  20. Determination of geochemical distribution of platinum elements in chromites and related minerals using neutron activation analysis technique

    International Nuclear Information System (INIS)

    Agiorgitis, G.

    1978-08-01

    Results of Pt, Pd, Ir, Os and Ru determination in various rocks and minerals using radiochemical neutron activation method are presented and geochemical correlations of the platinum elements studied. The method of analysis was described in detail in 4 progress reports

  1. 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)

  2. Determination of the elemental distribution in cigarette components and smoke by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Wu, D.; Landsberger, S.; Larson, S.M.

    1997-01-01

    Cigarette smoking is a major source of particle released in indoor environments. A comprehensive study of the elemental distribution in cigarettes and cigarette smoke has been completed. Specifically, concentrations of thirty elements have been determined for the components of 15 types of cigarettes. Components include tobacco, ash, butts, filters, and cigarette paper. In addition, particulate matter from mainstream smoke (MS) and sidesstream smoke (SS) were analyzed. The technique of elemental determination used in the study is instrumental neutron activation analysis. The results show that certain heavy metals, such as As, Cd, K, Sb and Zn, are released into the MS and SS. These metals may then be part of the health risk of exposure to smoke. Other elements are retained, for the most part, in cigarette ash and butts. The elemental distribution among the cigarette components and smoke changes for different smoking conditions. (author)

  3. 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)

  4. Application of neutron activation analysis for determination of elements in field of public health science

    International Nuclear Information System (INIS)

    Iijima, Ikuyo

    2010-01-01

    Outline of neutron activation analysis (NAA) and application examples of this method to ensure safety of food and environment are explained. It consists of four chapters such as introduction, what is NAA, quality control of NAA, application examples of NAA for determination of the elements in the field of public health science. The quality control of NAA is carried out by using certified reference materials, identification of individual difference of sample, and homogeneity of samples. Some application examples of NAA for determination Cd in rice, Hg and As in fish, U in soil, food and aerosol, 128 I and 129 I in environment, Cs and 133 Cs in mushroom, the essential elements and trace elements in food are reported. Analytical results of elements in certified reference materials, content of elements in ashed samples (carrots and bamboo shoots), average use frequency of ingredients in a sample, and correlation between Cs and 137 Cs in mushroom are illustrated. (S.Y.)

  5. Concentration of 17 Elements in Subcellular Fractions of Beef Heart Tissue Determined by Neutron Activation Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Wester, P O

    1964-12-15

    Subcellular fractions of beef heart tissue are investigated, by means of neutron activation analysis, with respect to their concentration of 17 different elements. A recently developed ion-exchange technique combined with gamma spectrometry is used. The homogeneity of the subcellular fractions is examined electron microscopically. The following elements are determined: As, Ba, Br, Cas Co, Cs, Cu, Fe, Hg, La, Mo, P, Rb, Se, Sm, W and Zn. The determination of Ag, Au, Cd, Ce, Cr, Sb and Sc is omitted, in view of contamination. Reproducible and characteristic patterns of distribution are obtained for all elements studied.

  6. Concentration of 17 Elements in Subcellular Fractions of Beef Heart Tissue Determined by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Wester, P.O.

    1964-12-01

    Subcellular fractions of beef heart tissue are investigated, by means of neutron activation analysis, with respect to their concentration of 17 different elements. A recently developed ion-exchange technique combined with gamma spectrometry is used. The homogeneity of the subcellular fractions is examined electron microscopically. The following elements are determined: As, Ba, Br, Cas Co, Cs, Cu, Fe, Hg, La, Mo, P, Rb, Se, Sm, W and Zn. The determination of Ag, Au, Cd, Ce, Cr, Sb and Sc is omitted, in view of contamination. Reproducible and characteristic patterns of distribution are obtained for all elements studied

  7. Determination of essential elements in edible seaweed by neutron activation analysis

    International Nuclear Information System (INIS)

    Alves, Cassio Bessa Lima; Maihara, Vera Akiko

    2013-01-01

    Comestible marine algae are gaining wider global trade, not only because of the taste but also the nutritional quality they present. They are rich in protein, fiber, vitamins and are excellent sources of essential elements due to their ability to absorb substances storing them in their bodies. its chemical composition varies according to the species, habitat, maturity and environmental conditions which are submitted. The method of Neutron Activation Analysis was used to determine the essential elements Cl, K, Mg, Mn and Na present in marine algae from different countries, which are sold in the city of Sao Paulo. A total of 6 samples of marine algae were analyzed, 4 species of Nori (Porphyra umbilicates) from China, Korea, Japan and USA; 1 of Hijiki (Hijikia fusiforme) species from Japan; and 1 species of Kombu (Laminaria sp.) of South Korea. To validate the methodology used was the reference material NIST SRM 1577b Bovine Liver. The concentrations range from 5265-1175 μg/g to CL; from 14413-90261 μg/g to K; from 3007-7091 μg/g to Mg; from 2,3-33,8 μg/g to Mn and from 5161-24973 μg/g to Na

  8. Presentation

    Directory of Open Access Journals (Sweden)

    Eduardo Vicente

    2013-06-01

    Full Text Available In the present edition of Significação – Scientific Journal for Audiovisual Culture and in the others to follow something new is brought: the presence of thematic dossiers which are to be organized by invited scholars. The appointed subject for the very first one of them was Radio and the invited scholar, Eduardo Vicente, professor at the Graduate Course in Audiovisual and at the Postgraduate Program in Audiovisual Media and Processes of the School of Communication and Arts of the University of São Paulo (ECA-USP. Entitled Radio Beyond Borders the dossier gathers six articles and the intention of reuniting works on the perspectives of usage of such media as much as on the new possibilities of aesthetical experimenting being build up for it, especially considering the new digital technologies and technological convergences. It also intends to present works with original theoretical approach and original reflections able to reset the way we look at what is today already a centennial media. Having broadened the meaning of “beyond borders”, four foreign authors were invited to join the dossier. This is the first time they are being published in this country and so, in all cases, the articles where either written or translated into Portuguese.The dossier begins with “Radio is dead…Long live to the sound”, which is the transcription of a thought provoking lecture given by Armand Balsebre (Autonomous University of Barcelona – one of the most influential authors in the world on the Radio study field. It addresses the challenges such media is to face so that it can become “a new sound media, in the context of a new soundscape or sound-sphere, for the new listeners”. Andrew Dubber (Birmingham City University regarding the challenges posed by a Digital Era argues for a theoretical approach in radio studies which can consider a Media Ecology. The author understands the form and discourse of radio as a negotiation of affordances and

  9. Determination of toxic and essential element concentrations in foodstuffs from local market

    International Nuclear Information System (INIS)

    Surtipanti; Suwirma; Yumiarti; June, M.; Syaifudin, S.

    1989-01-01

    Determination of toxic and essential elements concentrations in foodstuffs from local market in Jakarta. Concentration of toxic essential elements, such as, As, Hg, Cr, Pb, Cu, and Zn, in rice, corn bean, small green peas, wheat, vegetables, fruits, tea and coffee, have been determined. As, Hg, Sb, Cr, Se, and Zn, were determined using neutron activation analysis, after being irradiated at TRIGA-MARK II reactor, while Pb and Cu were determined using atomic absorption spectrophotometer. The results obtained were lower than the maximum permissible concentration allowed. (author). 8 refs

  10. 5 CFR 847.603 - Date of present value and deficiency determinations.

    Science.gov (United States)

    2010-01-01

    ... 5 Administrative Personnel 2 2010-01-01 2010-01-01 false Date of present value and deficiency... of present value and deficiency determinations. (a) For determining the deficiency under § 847.604, OPM will determine, under §§ 847.605 through 847.607, the present values of future retirement benefits...

  11. [Study on the determination of 14 inorganic elements in coffee by inductively coupled plasma mass spectrometry].

    Science.gov (United States)

    Nie, Xi-Du; Fu, Liang

    2013-07-01

    Samples of coffee were digested by microwave digestion, and inorganic elements amounts of Na, Mg, P, Ca, Cr, Mn, Fe, Co, Cu, Zn, As, Se, Mo and Pb in sample solutions were determined by inductively coupled plasma mass spectrometry (ICP-MS). HNO3 + H2O2 was used to achieve the complete decomposition of the organic matrix in a closed-vessel microwave oven. The working parameters of the instrument were optimized. The results showed that the relative standard deviation (RSD) was less than 3.84% for all the elements, and the recovery was found to be 92.00% -106.52% by adding standard recovery experiment. This method was simple, sensitive and precise and can perform simultaneous multi-elements determination of coffee, which could satisfy the sample examination request and provide scientific rationale for determining inorganic elements of coffee.

  12. Determination of 28 elements in American cigarette tobacco by neutron-activation analysis

    International Nuclear Information System (INIS)

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

    1986-01-01

    The concentrations of 28 toxic and other elements in cigarette tobacco of twelve brands commercially manufactured in the USA were determined using instrumental neutron-activation analysis. The elements determined were Al, As, Ba, Br, Ca, Ce, Cl, Co, Cr, Cs, Eu, Fe, Hf, K, La, Mg, Mn, Na, Ni, Rb, Sb, Sc, Se, Sr, Th, Ti, V and Zn. The concentrations of the determined elements in the American cigarettes were compared with the elemental concentrations reported for Iranian, Pakistani and Japanese brands. It was concluded that the concentrations of As, Br, Ca, Eu, K and Zn in the samples under investigation are lower than those reported for the analysis of University of Kentucky reference cigarettes, whereas the concentrations of Mn and Na are higher. The contents of Al, Cl, Co, Cr, Cs, Fe, La, Sb, Sc, and Se are similar to those in the reference cigarettes. (author)

  13. The determination of the rare earth elements in naturally-occurring materials zy flame spectroscopy

    International Nuclear Information System (INIS)

    Watts, J.C.

    1975-01-01

    Because the quantitative collection of the rare-earth elements retains natural abundance ratios, adequate analytical methodology incorporates their individual sensitivities, and tolerates their mutual contamination. To achieve these ends, the sensitivities of 15 rare-earths in flame emission were determined in the unseparated nitrous oxide/acetylene flame, their mutual interference ascertained at practical concentrations, and useful emission lines selected for their determination in natural materials. Sources of atomic emission interference were extraneous in origin. Fe in the determination of Dy and Zr in the determination of Nd. Inter-element interferences of the rare-earth elements were minimal after wavelength selection and reduction of the spectral band width. For comparison, five rare earths were determined by flame AAS. (author)

  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. 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)

  16. Determination of rare earth elements by liquid chromatographic separation using inductively coupled plasma mass spectrometric detection

    International Nuclear Information System (INIS)

    Braverman, D.S.

    1992-01-01

    High-performance liquid chromatography (HPLC) is used to separate the rare earth elements (REEs) prior to detection by inductively coupled plasma mass spectrometry (ICP-MS). The use of HPLC-ICP-MS in series combines the separation power and speed of HPLC with the sensitivity, isotopic selectivity and speed of ICP-MS. The detection limits for the REEs are in the sub-ng ml -1 range and the response is linear over four orders of magnitude. A preliminary comparison of isotope dilution and external standard results for the determination of REEs in National Institute of Standards and Technology (NIST) Standard Reference Material (SRM 1633a) Fly Ash is presented. (author)

  17. 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

  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. (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).

  20. 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

  1. Determination of elements in concrete of a nuclear accelerator to dismantle, by instrumental neutron activation analysis, ICPMS and ICPAES

    International Nuclear Information System (INIS)

    Gaudry, A.; Bertho, X.; Piccot, D.; Fougeron, C.

    1998-01-01

    The distribution of radionuclides and their radioactivity in irradiated waste concrete are modelled using the characteristics of nuclear particle fluxes integrated all during the life-time of the installation, chemical composition of the material, and activation parameters of nuclear reactions produced by particles and secondary neutrons on elements. This paper describes the techniques used for determining the chemical composition of trace elements radioactivated by neutrons and particles, but also the major elements which act upon the neutron penetration into the depth of the concrete. Major elements were determined using mainly, Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES) for Si, Al, Fe, Mn, Mg, Ca, Na, K, Ti, P and Instrumental Neutron Activation Analysis (INAA) for Al, Mn, Fe, Mg, Ca, Ba, Na, K, and other specific methods for C, O, S, and H. Trace elements were also determined using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and INAA. Forty five elements were determined. When present, solid iron was separated by a magnetic bar after previous breaking of the concrete. The concrete was powdered to a granulometry of less than 0.5 mm for INAA and homogenized. Iron was determined separately by INAA. For the determinations by ICP-AES and ICP-MS, powders were previously fused by means of LiBO 2 , then dissolved in dilute HNO 3 before analysis. A comparison between the results obtained, on the one hand, by ICP-AES and INAA, on the second hand, by ICP-MS and INAA revealed generally a very good agreement, making consistent analytical results

  2. The determination of sulfur and some heavy elements in the coke

    International Nuclear Information System (INIS)

    Ma'rouf, M.

    2003-01-01

    The content of free sulfur and some heavy elements in the coke resulting from the residua of oil industry was determined bu using various technical analytical methods. The flame technique of atomic absorption FAAS was used to identify lead, copper, zinc, chromium, VGA-AAS and determine arsenic and selenium, CV-AAS to the determination of mercury. As for sulfur, it was determined by using the total oxidation method at high temperatures (1100 C 0 ). The IR indicator was used for further determination. The relative standard deviation in the determination of sulfur did not exceed the limits of 0.01 and 0.02, compared to the determination of other elements by using the atomic absorption method. (Author)

  3. Determination of planetary surfaces elemental composition by gamma and neutron spectroscopy

    International Nuclear Information System (INIS)

    Diez, B.

    2009-06-01

    Measuring the neutron and gamma ray fluxes produced by the interaction of galactic cosmic rays with planetary surfaces allow constraining the chemical composition of the upper tens of centimeters of material. Two different angles are proposed to study neutron and gamma spectroscopy: data processing and data interpretation. The present work is in line with two experiments, the Mars Odyssey Neutron Spectrometer (MONS) and the Selene Gamma Ray Spectrometer. A review of the processing operations applied to the MONS dataset is proposed. The resulting dataset is used to determine the depth of the hydrogen deposits below the Martian surface. In water depleted regions, neutron data allow constraining the concentration in elements likely to interact with neutrons. The confrontation of these results to those issued from the Gamma Ray Spectrometer onboard Mars Odyssey provides interesting insight on the geologic context of the Central Elysium Planitia region. These martian questions are followed by the study of the Selene gamma ray data. Although only preliminary processing has been done to date, qualitative lunar maps of major elements (Fe, Ca, Si, Ti, Mg, K, Th, U) have already been realized. (author)

  4. Determination of elemental composition in dietary supplements by neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Vitor I.; Saiki, Mitiko, E-mail: vitor.ito@outlook.com, E-mail: mitiko@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2015-07-01

    Dietary supplements intake has grown in the last years because of their potential health benefits. This supplementation is very common among athletes, elderly population and consumers that want to increase the total daily nutrient intake. Consequently, elemental composition evaluation in these supplements is of great interest due to its increasingly high consumption and the brand variety offered in the market. This study aimed to evaluate the elemental composition in three types of dietary supplements acquired in a pharmacy and drugstore in Sao Paulo city. Concentrations of As, Br, Ca, Co, Cr, Cu, Fe, K, La, Na, Sb, Sc, Se and Zn were determined in these supplements by applying neutron activation analysis (NAA) followed by a gamma ray spectrometry. from the concentrations obtained in the dietary supplement analyses, the data obtained were compared to the values presented on the product label. These comparisons indicated in general, a good agreement of the data obtained and the values of the product label depending on the supplement. From the results obtained it can be concluded that NAA is an important tool for the analysis of this type of products due to its reliability of results and its multielemental character. (author)

  5. Determination of elemental composition in dietary supplements by neutron activation analysis

    International Nuclear Information System (INIS)

    Souza, Vitor I.; Saiki, Mitiko

    2015-01-01

    Dietary supplements intake has grown in the last years because of their potential health benefits. This supplementation is very common among athletes, elderly population and consumers that want to increase the total daily nutrient intake. Consequently, elemental composition evaluation in these supplements is of great interest due to its increasingly high consumption and the brand variety offered in the market. This study aimed to evaluate the elemental composition in three types of dietary supplements acquired in a pharmacy and drugstore in Sao Paulo city. Concentrations of As, Br, Ca, Co, Cr, Cu, Fe, K, La, Na, Sb, Sc, Se and Zn were determined in these supplements by applying neutron activation analysis (NAA) followed by a gamma ray spectrometry. from the concentrations obtained in the dietary supplement analyses, the data obtained were compared to the values presented on the product label. These comparisons indicated in general, a good agreement of the data obtained and the values of the product label depending on the supplement. From the results obtained it can be concluded that NAA is an important tool for the analysis of this type of products due to its reliability of results and its multielemental character. (author)

  6. Determination of chemical elements in Eucalyptus grandis, manured with Ballad's, by neutrons activation analysis

    International Nuclear Information System (INIS)

    Mateus, Natalina de Fatima; Madi Filho, Tufic

    2007-01-01

    The biosolid is a mud resulting from the biological treatment of wasted liquids. It is considered as a profitable alternative and important to minimize the environmental impact generated by the sewage thrown in to sanitary lands, in forest cultures like the Eucalyptus grandis. The objective of this work was to detect which chemical elements are present in Eucalyptus grandis samples, fertilized with different quantities of biosolid. The eucalyptuses of Estacao Experimental de Ciencias Florestais of Itatinga were planted in March of 1998 and collected with five years old. The used biosolid was produced by Station of Treatment of Sewer of Barueri - SP, classified as kind B. For the determination of the presence and quantity of chemical elements in the eucalyptus samples, an analysis technique by neutronic activation (NAA) was used followed by gamma rays spectroscopy. The samples were irradiated in the Nuclear Reactor IEA-R1 of IPEN-SP, followed by the measure of induced gamma rays activity, using a Detector HPGe. The presence, mainly of Br, Mn, Na and K, was detected in all analyzed samples. (author)

  7. Molecular analysis of an integrative conjugative element, ICEH, present in the chromosome of different strains of Mycoplasma hyopneumoniae

    Directory of Open Access Journals (Sweden)

    Paulo Marcos Pinto

    2007-01-01

    Full Text Available Diversification of bacterial species and pathotypes is largely caused by lateral gene transfer (LGT of diverse mobile DNA elements such as plasmids, phages, transposons and genomic islands. Thus, acquisition of new phenotypes by LGT is very important for bacterial evolution and relationship with hosts. This paper reports a 23 kb region containing fourteen CDSs with similarity to the previous described Integrative Conjugal Element of Mycoplasma fermentans (ICEF. This element, named ICEH, is present as one copy at distinct integration sites in the chromosome of 7448 and 232 pathogenic strains and is absent in the type strain J (non-pathogenic. Notable differences in the nucleotide composition of the insertion sites were detected, and could be correlated to a lack of specificity of the ICEH integrase. Although present in strains of the same organism, the ICEH elements are more divergent than the typical similarity between other chromosomal locus of Mycoplasma hyopneunomiae, suggesting an accelerated evolution of these constins or an ongoing process of degeneration, while maintaining conservation of the tra genes. An extrachromosomal form of this element had been detected in the 7448 strain, suggesting a possible involvement in its mobilization and transference of CDSs to new hosts.

  8. A review of electro analytical determinations of some important elements (Zn, Se, As) in environmental samples

    International Nuclear Information System (INIS)

    Lichiang; James, B.D.; Magee, R.J.

    1991-01-01

    This review covers electro analytical methods reported in the literature for the determination of zinc, cadmium, selenium and arsenic in environmental and biological samples. A comprehensive survey of electro analytical techniques used for the determination of four important elements, i.e. zinc, cadmium, selenium and arsenic is reported herein with 322 references up to 1990. (Orig./A.B.)

  9. Determination of the stability constants for the complexes of rare-earth elements and tetracycline

    International Nuclear Information System (INIS)

    Saiki, M.; Lima, F.W.

    1977-01-01

    Stability constants for the lanthanide elements complexes with tetracycline were determined by the methods of average number of ligands, the two parameters and by weighted least squares. The technique of solvent extraction was applied to obtain the values of the parameters required for the determination of the constants [pt

  10. 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

  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. 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

  13. 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.)

  14. 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).

  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. Total reflection X-ray Fluorescence determination of interfering elements rubidium and uranium by profile fitting

    Science.gov (United States)

    Dhara, Sangita; Khooha, Ajay; Singh, Ajit Kumar; Tiwari, M. K.; Misra, N. L.

    2018-06-01

    Systematic studies to assess the analytical parameters obtained in the total reflection X-ray fluorescence (TXRF) determinations of interfering elements Rb and U using profile fitting are reported in the present manuscript. The X-ray lines Rb Kα and U Lα having serious spectral interference (ΔE = 218 eV), have been used as analytical lines. The intensities of these X-ray lines have been assessed using profile fitting. In order to compare the analytical results of Rb determinations in presence of U, with and without U excitation, synchrotron radiation was tuned to energy just above and below the U Labs edge. This approach shall excite both Rb Kα and U Lα simultaneously and Rb Kα selectively. Finally, the samples were also analyzed with a laboratory based TXRF spectrometer. The analytical results obtained in all these conditions were comparable. The authenticity of the results was assessed by analyzing U with respect to Rb in Rb2U(SO4)3, a standard reference material for U. The average precision obtained for TXRF determinations was below 3% (RSD, n = 3, 1σ) and the percent deviation of TXRF values from the expected values calculated on the basis of sample preparation was within 3%.

  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. Determination of Inorganic Elements in White Rice by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Moon, J. H.; Kim, S. H.; Lim, J. M.; Lee, Y. N.; Chung, Y. S.

    2011-01-01

    Rice is a staple food and provides an important information of mineral supplement as well as a large portion of calorie for Korean. As scientists have focused their researches on health impacts caused by mineral nutrient deficiency and hazardous elements, public concerns about mineral intake by dietary food is rising. The objectives of this study were to determine inorganic elemental contents in white rice by neutron activation analysis(NAA) and to assist the evaluation of nutritional and harmful status for Korean people

  19. Determination of overall decontamination factors for common impurity elements in PHWR spent fuel reprocessing

    International Nuclear Information System (INIS)

    Pant, D.K.; Bhalerao, B.A.; Gupta, K.K.; Kulkarni, P.G.; Gurba, P.B.; Janardan, P.; Changrani, R.D.; Dey, P.K.

    2009-01-01

    An attempt has been made to determine overall decontamination factors for elemental impurities normally encountered in the U 3 O 8 product obtained by reprocessing of PHWR spent fuel. The solution obtained by dissolution of spent fuel and corresponding U 3 O 8 product were analyzed for 24 elemental impurities by ICP-AES for this purpose. Decontamination factors achieved for major neutron poisons are in the range of 200-400. (author)

  20. 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

  1. 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

  2. Application of paper chromatography to the determination of some elements in minerals and rocks

    International Nuclear Information System (INIS)

    Agrinier, H.

    1964-11-01

    This publication describes our work in applying paper chromatography to the fields of mineralogy and geology. We have studied the separation and determination of the following elements: Nb, Ta, Ti, Co, Cu, Mn, Sn, Ge, As, Sb, Bi, U, Th, Be, Au, Pb, Zn, V and Mo. The development of separation methods for these various elements has led us to solve many interference problems. These methods make it possible to separate and measure mineral components. They also enable us to search for trace elements in ores, rocks soils and carbonaceous materials. Finally let us point out that this technique may equally be used for analysis in very radioactive environment. (author) [fr

  3. Determination of essential and toxic elements in commercially available fruit juices

    International Nuclear Information System (INIS)

    Yawar, W.; Rahman, S.

    1997-01-01

    A study has been carried out for the determination of Cr, Pb, Fe in different varieties of commercially available packed fruit juices like apple, mango orange and mixed flavour by using flame and electrothermal atomic absorption spectrophotometric technique. These juices are available at a reasonable price and are commonly used by public. Like many other articles the baseline levels of essential and toxic elements in Pakistani fruit juices are generally not available. It was, therefore, considered to monitor the levels of essential as well toxic elements in the juices. Hence a variety of juices was collected from local market and measurements of the above mentioned elements were made. (author)

  4. The k0 and relative INAA methods to determine elements in entire archaeological pottery objects

    International Nuclear Information System (INIS)

    Bedregal, P.S.; Mendoza, P.A.; Ubillus, M.S.; Montoya, E.H.; Cohen, I.M.; Universidad Tecnologica Nacional, Buenos Aires

    2014-01-01

    The advantages of instrumental neutron activation analysis applied to archaeological ceramics have been enhanced through the analysis of entire objects, using both the k 0 method and the relative method, respectively, to determine the concentrations of chemical elements in aliquots of replicate objects used as comparators and in the sample object. Twenty-two chemical elements of archaeological importance were measured in mud figurines from Caral civilization (5000 year BC), irradiated inside a well-characterized radial channel facility of the nuclear research reactor at IPEN, Peru. The results showed less than 10 % of bias for most of the elements. (author)

  5. 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)

  6. 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.

  7. Simplified Qualitative Discrete Numerical Model to Determine Cracking Pattern in Brittle Materials by Means of Finite Element Method

    Directory of Open Access Journals (Sweden)

    J. Ochoa-Avendaño

    2017-01-01

    Full Text Available This paper presents the formulation, implementation, and validation of a simplified qualitative model to determine the crack path of solids considering static loads, infinitesimal strain, and plane stress condition. This model is based on finite element method with a special meshing technique, where nonlinear link elements are included between the faces of the linear triangular elements. The stiffness loss of some link elements represents the crack opening. Three experimental tests of bending beams are simulated, where the cracking pattern calculated with the proposed numerical model is similar to experimental result. The advantages of the proposed model compared to discrete crack approaches with interface elements can be the implementation simplicity, the numerical stability, and the very low computational cost. The simulation with greater values of the initial stiffness of the link elements does not affect the discontinuity path and the stability of the numerical solution. The exploded mesh procedure presented in this model avoids a complex nonlinear analysis and regenerative or adaptive meshes.

  8. Element determination of fine particles in environmental aerosols using PIXE; Determinacion elemental de paticulas finas en aerosoles ambientales usando PIXE

    Energy Technology Data Exchange (ETDEWEB)

    Garcia O, B. [ITT, 50000 Toluca (Mexico); Aldape U, F. [ININ, 52750 La Marquesa, Estado de Mexico (Mexico)]. e-mail: gaolivab@gmail.com

    2007-07-01

    The Mexico city is classified as one of the more populated cities of the world which presents a decrease in the air quality and that gives place to a severe problematic in atmospheric pollution. To cooperate in the solution of this problem it is necessary to carry out studies that allow a better knowledge of the atmosphere of the city. This study presents the results of a monitoring campaign of fine particle carried out from September 21 to December 12, 2001 in three sites of the Mexico City center area. The samples were collected every third day with a collector type unit of heaped filters (Gent). The analysis of these samples was carried out in the 2 MV accelerator of the National Institute of Nuclear Research (ININ) applying the PIXE technique and with this analysis its were identified in the samples approximately 15 elements in each one of the 3 sites and was calculated the concentration in that its were present. With these results a database was created and by means of it mathematical treatment the Enrichment factor (FE), the time series of each element and the multiple correlation matrix were evaluated. The obtained results showed that the Civil Registration site (Salto del Agua) it was the more polluted coinciding that to a bigger concentration of activities a bigger increase in the pollution is generated. (Author)

  9. Determining the elemental composition of fuels by bomb calorimetry and the inverse correlation of HHV with elemental composition

    Energy Technology Data Exchange (ETDEWEB)

    Bech, Niels; Jensen, Peter Arendt; Dam-Johansen, Kim [Department of Chemical and Biochemical Engineering, CHEC Research Centre, Technical University of Denmark, Soeltofts Plads, Building 229, DK-2800 Kongens Lyngby (Denmark)

    2009-03-15

    This article presents a method to obtain a simplified elemental analysis of an organic sample in which oxygen, nitrogen, and sulphur are lumped. The method uses a bomb calorimeter, water, and ash measurements combined with a numerical procedure based on a generalised equation for predicting higher heating value. By analysing pure organic substances, literature data, and fuels it is demonstrated that the method can provide hydrogen estimates within {+-}0.7% daf. and carbon and sum of oxygen, nitrogen, and sulphur estimates within {+-}2% daf. for fuels containing less than 90% ash db., 2% nitrogen daf., and 1% daf. sulphur. (author)

  10. 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

  11. 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.

  12. 5 CFR 847.605 - Methodology for determining the present value of annuity with service credit.

    Science.gov (United States)

    2010-01-01

    ... Retroactive Provisions § 847.605 Methodology for determining the present value of annuity with service credit. (a) OPM will determine the present value of the annuity including service credit for NAFI service..., the present value under paragraph (a) of this section equals the monthly annuity rate including credit...

  13. Burnup determination of power reactor fuel elements by gamma spectrometry; Determination par spectrometrie {gamma} du taux d'irradiation des elements combustibles des reacteurs de puissance

    Energy Technology Data Exchange (ETDEWEB)

    Robin, M; Jastrzeb, M; Boisliveau, S; Boyer, R; Vidal, R [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1969-07-01

    This report describes a method for determining by {gamma} spectrometry the burn up and the specific power of fuel elements irradiated in power reactors. The energy spectrum of {gamma} rays emitted by fission products is measured by means of a simple equipment using a sodium iodide detector and a multichannel analyzer. In order to extract from the spectrum a quantity proportional to the burn up, it is necessary to: - isolate an activity specific of one emitter,- give the same importance to fissions in uranium and plutonium - take into account the radioactive decay during and after irradiation. One hundred fuel elements were studied and burn up values obtained by {gamma} spectrometry are compared to results given by chemical analyses. Preliminary measurements show that the accuracy of the results is greatly increased by the use of a germanium detector, due to its good resolution. (authors) [French] Ce rapport expose une methode de determination par spectrometrie {gamma} du taux d'irradiation et de la puissance specifique des elements combustibles irradies dans les reacteurs de puissance. Une installation simple utilisant un detecteur d'iodure de sodium et un selecteur multicanaux mesure le spectre en energie du rayonnement {gamma} emis par les produits de fission. Afin d'extraire du spectre une quantite proportionnelle au taux de combustion, il faut: - isoler une activite specifique a un emetteur, - donner la meme importance aux fissions survenues dans l'uranium et le plutonium, - prendre en compte la decroissance radioactive pendant et apres l'irradiation. Les mesures ont porte sur une centaine d'elements combustibles et les taux de combustion obtenus par spectrometrie {gamma} sont compares aux resultats des analyses chimiques. Des mesures preliminaires montrent que l'utilisation d'un detecteur de germanium augmente considerablement la precision des resultats, en raison de son excellente resolution. (auteurs)

  14. 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)

  15. 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.

  16. 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)

  17. Fuel element burnup determination in HEU-LEU mixed TRIGA research reactor core

    International Nuclear Information System (INIS)

    Zagar, Tomaz; Ravnik, Matjaz

    2000-01-01

    This paper presents the results of a burnup calculations and burnup measurements for TRIGA FLIP HEU fuel elements and standard TRIGA LEU fuel elements used simultaneously in small TRIGA Mark II research reactor in Ljubljana, Slovenija. The fuel element burnup for approximately 15 years of operation was calculated with two different in house computer codes TRIGAP and TRIGLAV (both codes are available at OECD NEA Data Bank). The calculation is performed in one-dimensional radial geometry in TRIGAP and in two-dimensional (r,φ) geometry in TRIGLAV. Inter-comparison of results shows important influence of in-core water gaps, irradiation channels and mixed rings on burnup calculation accuracy. Burnup of 5 HEU and 27 LEU fuel elements was also measured with reactivity method. Measured and calculated burnup values are inter-compared for these elements (author)

  18. 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)

  19. Environmental pollution studies. Quantitative determination of elements in the air particulate matter by NAA

    International Nuclear Information System (INIS)

    Sutisna; Hidayat, Achmad; Muhayatun; Supriatna, Dadang

    2006-01-01

    Regarding to the 2002 PNCA Program for the Utilization of INAA in the Environmental Study, the elemental determination of air particulate matter have been done. Two sampling site were chosen to collect a PMs samples, i.e. Lembang and Bandung that represent the rural and the urban region respectively. The period of sampling was January 2002 to November 2002. Air sample was collect by GANT Stacked air sampler using 47 mm diameter cellulose filter which have a pore size of 0.45 μm and 8 μm for fine and coarse particle respectively. Quantitative elemental determination has been done using Instrumental Neutron Activation Analysis based on a comparative method. The elemental distributions on fine and coarse fraction of air particulate matter have been analyzed for both sampling sites as well as the enrichment factor (EF) for all elements interest. The result shows that the average annual concentrations of fine and coarse PMs in the Lembang sampling site were 7.8 μg.m -3 and 1.6 μg.m -3 respectively. Meanwhile at Bandung sampling site, the PMs are higher than that a Lembang sampling site, i.e. 14.4 μg.m -3 and 22.5 μg.m -3 for fine and coarse PMs respectively. The fine fraction was higher than the coarse fraction at Lembang sampling site, but at Bandung sampling site the fine fraction was lower than the coarse fraction. Fifteen elements of Na, Al, V, Mn, Br, I, Cl, Sc, Co, Fe, Cr, Zn, La, Sb and Sm were analyzed for both sampling site. Among those elements concerned, Na, Al, Br, Cl and Fe were major constituent elements in all fractions that have a concentration more than 40 ng.cm -3 . Generally, the concentration of elements determined in the urban sampling site was higher than that in the rural site. Al, V, Mn, Sc, Co and Fe are relatively higher in concentration in coarse fraction of urban site. Br element concentration was not significantly different for both sampling site. The EF values of most elements concerned are generally also higher for the fine fraction

  20. Determination of aluminium, scandium and rare earth elements by emission flame spectrometry

    International Nuclear Information System (INIS)

    Otruba, V.; Sommer, L.

    1989-01-01

    Emission spectrometry in nitrous oxide-acetylene flames in combination with a highly resolving double monochromator and sensitive detecting system enables simple, sensitive and selective determinations of aluminium, scandium and all rare earth elements with exception of cerium in complicated matrices. Calibration plots are linear for a large concentration interval (≤ 100 μgxml -1 ), detection limits are in ngxml -1 level and RSD does not exceed 3% on the optimal concentration level of the particular element. The determination of Al, Sc, Eu and Yb showed particular advantages as to methods using ICP-spectrometry. (orig.)

  1. Determination of some elements in bottom sediments from Varna Bay, Bulgaria, and Saronikos Gluf, Greece

    International Nuclear Information System (INIS)

    Apostolov, D.; Jovchev, M.; Kinova, L.; Nikolov, P.; Penev, I.; Taskaev, E.; Grigorov, T.; Stoyanov, A.

    1985-01-01

    The concentrations of 16 trace elements (Ce, Co, Cr, Eu, Cs, Fe, Hf, La, Mg, Mn, Rb, Sb, Sc, Sm and V) in bottom sediments and in flesh and liver of Gobius niger were determined by means of instrumental neutron activation analysis. The samples were collected from the upper 5 cm layer of of the bottom sedimements together with fish from 5 points of Varna Bay and from 2 points of Saronicos Gulf in the summer of 1980. The results obtained proved to be important in investigating the ecological role of elements determined in connection with human activity in the studied area

  2. The microwave induced plasma with optical emission spectrometry (MIP-OES) in 23 elements determination in geological samples.

    Science.gov (United States)

    Niedzielski, P; Kozak, L; Wachelka, M; Jakubowski, K; Wybieralska, J

    2015-01-01

    The article presents the optimisation, validation and application of the microwave induced plasma optical emission spectrometry (MIP-OES) dedicated for a routine determination of Ag, Al, B, Ba, Bi, Ca, Cd, Cr, Cu, Fe, Ga, In, K, Li, Mg, Mn, Mo, Na, Ni, Pb, Sr, Tl, Zn, in the geological samples. The three procedures of sample preparation has been proposed: sample digestion with the use of hydrofluoric acid for determination of total concentration of elements, extraction by aqua regia for determination of the quasi-total element concentration and extraction by hydrochloric acid solution to determine contents of the elements in acid leachable fraction. The detection limits were on the level 0.001-0.121 mg L(-1) (from 0.010-0.10 to 1.2-12 mg kg(-1) depend on the samples preparation procedure); the precision: 0.20-1.37%; accuracy 85-115% (for recovery for certified standards materials analysis and parallel analysis by independent analytical techniques: X-ray fluorescence (XRF) and flame absorption spectrometry (FAAS)). The conformity of the results obtained by MIP-OES analytical procedures with the results obtained by XRF and FAAS analysis allows to propose the procedures for studies of elemental composition of the fraction of the geological samples. Additionally, the MIP-OES technique is much less expensive than ICP techniques and much less time-consuming than AAS techniques. Copyright © 2014 Elsevier B.V. All rights reserved.

  3. Crystalline Ultrastructures, Inflammatory Elements, and Neoangiogenesis Are Present in Inconspicuous Aortic Valve Tissue

    Directory of Open Access Journals (Sweden)

    P. Dorfmüller

    2010-01-01

    Full Text Available Morbidity from calcific aortic valve disease (CAVD is increasing. Recent studies suggest early reversible changes involving inflammation and neoangiogenesis. We hypothesized that microcalcifications, chemokines, and growth factors are present in unaffected regions of calcific aortic valves. We studied aortic valves from 4 patients with CAVD and from 1 control, using immunohistochemistry, scanning electron microscopy, and infrared spectrography. We revealed clusters of capillary neovessels in calcified (ECC, to a lesser extent in noncalcified (ECN areas. Endothelial cells proved constant expression of SDF-1 in ECC, ECN, and endothelial cells from valvular surface (ECS. Its receptor CXCR4 was expressed in ECC. IL-6 expression correlated with CXCR4 staining and presence of lymphocytes. VEGF was expressed by ECS, its receptor by ECC and ECN. Crystalline ultrastructures were found on the surface of histologically noncalcified areas (HNCAs, spectrography revealed calcium hydroxylapatite. Our results demonstrate that crystalline ultrastructures are present in HNCAs, undergoing neoangiogenesis in an inflammatory context. These alterations could be an early witness of disease and an opening to therapy.

  4. 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

  5. [Determination of 27 elements in Maca nationality's medicine by microwave digestion ICP-MS].

    Science.gov (United States)

    Yu, Gui-fang; Zhong, Hai-jie; Hu, Jun-hua; Wang, Jing; Huang, Wen-zhe; Wang, Zhen-zhong; Xiao, Wei

    2015-12-01

    An analysis method has been established to test 27 elements (Li, Be, B, Mg, Al, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Sr, Mo, Cd, Sn, Sb, Ba, La, Hg, Pb, Bi) in Maca nationality's medicine with microwave digestion-ICP-MS. Sample solutions were analyzed by ICP-MS after microwave digestion, and the contents of elements were calculated according to their calibration curves, and internal standard method was adopted to reduce matrix effect and other interference effects. The experimental results showed that the linear relations of all the elements were very good; the correlation coefficient (r) was 0.9994-1.0000 (Hg was 0.9982) ; the limits of detection were 0.003-2.662 microg x L(-1); the relative standard deviations for all elements of reproducibility were lower than 5% (except the individual elements); the recovery rate were 78.5%-123.7% with RSD lower than 5% ( except the individual elements). The analytical results of standard material showed acceptable agreement with the certified values. This method was applicable to determinate the contents of multi-elements in Maca which had a high sensitivity, good specificity and good repeatability, and provide basis for the quality control of Maca.

  6. 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)

  7. Determination of elemental composition of some aphrodisiac herbs by Nuclear Analytical Technique (INAA)

    International Nuclear Information System (INIS)

    Mohammed, L.; Okunade, I.O.; Balogun, G.I.

    2011-01-01

    Fresh medicinal plants that are popularly believed to have aphrodisiac properties were collected in the form of leaves, stem bark, nuts, fruits, seeds, and roots, between 25th September 2009 and 15 October 2009. Instrumental Neutron Activation Analysis (INAA) has been applied to multielemental determination of thirteen aphrodisiac herbs used to treat the problem of Sexual dysfunction. Concentrations of twenty two elements AI, As, Ba, Br, Ca, Co, Cr, Cs, Dy, Eu, Fe, Hf, K, La, Lu, Mg, Mn, Na, Rb, Sb, Sc, Sm, Ta, Th, Ti, U, V, Yb, and Zn have been determined by short and long irradiation times with a thermal neutron flux of 5* 1011ncm-2s-1. Quality control and quality assurance of the method was tested by analyzing IAEA-359 and SRM-1573 together with the samples. The INAA spectra were analyzed using WINSPAN 2004 software package. Our result shows that Euphobia hirta recorded high Zn (669±34 g g-1) which is more than the amount (95.0 g g-1) in Jaipal sex tonic. The level of Fe in Cassytha filiformis, and Indigofera hirsute, is 599 g g-1 and 702 g g-1 respectively. These values are in good agreement with the Fe concentration in the popular aphrodisiac Panax gingseng and Radix codonopsis. For all the species of the same family the correlation coefficients are highly distinctive for each species. The present study can be use to some extent to assess the safety intake of aphrodisiac herbs in the final formulation.

  8. Determination of elements in cisadane river sediments by neutron activation analysis

    International Nuclear Information System (INIS)

    Kamarz, H.

    1997-01-01

    Determination of elements in Cisadane river sediments by neutron activation analysis has been conducted. Samples of sediments were obtained from some location along Cisadane river, i.e. Leuranji, Karanggan, Cibigo, Cisauk, Warung Mangga Pintu Air and Estuary Teluk Naga. the elements analysed were Al, Mn, Mg, V, K, Na, Fe, Cr, Co, U and Zn, and the results were compared to the SRM of sediment sample from IAEA. Generally, the results showed that the mean concentration of elements were found in Cibogo, Cisauk, Pintu Air and Muara Teluk Naga which were higher than others. Concentration factor of elements in sediments were in between of 0,02 - 3,45, this factor indicated that Cisadane river sediments have not been contaminated. CRM sediments 2704 from IAEA used as NAA Quality Control (author)

  9. 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.

  10. 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

  11. Comparison and determination of elemental composition in Korean space foods using instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Yong-Sam Chung; Sun-Ha Kim; Gwang-Min Sun; Jong-Hwa Moon; Jong-Il Choi; Beom-Seok Song; Jae-Hun Kim

    2013-01-01

    A quantitative analysis of mineral contents in several kinds of foods is needed to obtain information on a comprehensive elemental composition as well as an investigation on the effects of human health and nutrition based on the dietary intake of mineral elements. In 2012, six kinds of new Korean space foods (KSF) such as sweet pumpkin porridge, dakgalbi (spicy grilled chicken), Manila clam porridge, ox leg bone-cabbage soup, ginseng-chicken porridge, and chicken curry rice were developed by KAERI, and the contents of more than 15 elements in the samples were determined using an instrumental neutron activation analysis. A certified reference material associated with a biological food sample was used for analytical quality control. The analytical results were evaluated according to the elemental concentrations with KSF samples and compared with the reported values. These results will be applied toward the identification of gamma-irradiated foods. (author)

  12. Determination of 17 impurity elements in nuclear quality uranium compounds by atomic absorption spectroscopy

    International Nuclear Information System (INIS)

    Andonie, O.; Smith, L.A.; Cornejo, S.

    1985-01-01

    A method is described for the determination of 17 elements (Al, Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Mo, Na, Ni, Pb, V and Zn) in the ppm level, in nuclearly pure uranium compounds by flame atomic absorption spectroscopy. The analysis is performed by first dissolving the uranium sample in nitric acid and then extracting the uranium with tributyl phosphate solution. The aqueous phase, free of uranium, which contains the elements to analyze is inspirated into the flame of an atomic absorption spectrophotometer using air-acetylene or nitrous oxide-acetylene flame according to the element in study. This method allows to extract the uranium selectively in more than 99.0% and the recovery of the elements sudied was larger 90% (for K) to 100% (for Cr). The sensitivity of the method vary from 0.096 μg/g U (for Cd) to 5.5 μg/g U (for Na). (Author)

  13. 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

  14. 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)

  15. Determination of natural radioactivity and the concentration of elements in soil and plants at Krau Wildlife Reserve, Temerloh, Pahang

    International Nuclear Information System (INIS)

    Hafiz Hadzori

    2012-01-01

    This study was conducted to determine the natural radioactivity and the concentration of elements in soil and plants at Krau Wildlife Reserve, Pahang. Soil and plant samples collected were air dried and heated in the oven at temperature of 100 degree Celsius. Inductively Coupled Plasma Mass-Spectrometer (ICP-MS) was used to determine the natural radioactivity and elemental contents of each sample. Results showed that the concentration of U-238 and Th-232 varied from each sampling site. The concentration of Th-232 is higher than of U-238. For soil and plants samples, the natural radioactivity for both radionuclides were below 72 Bq/ kg. 15 elements present in both soil and plant samples, among other are Al, Fe, K, Mg, Mn, Ca, Zn, Co, Cd and As. The concentration of each elements differs for every sampling site. The elements with higher concentration are Al, Ca, Fe, K, Mg and Mn. This study showed that monocotyledon taking up more Mg than dicotyledons whereas dicotyledon plants taking up more Al. (author)

  16. Nonlinear modeling of ferroelectric-ferromagnetic composites based on condensed and finite element approaches (Presentation Video)

    Science.gov (United States)

    Ricoeur, Andreas; Lange, Stephan; Avakian, Artjom

    2015-04-01

    Magnetoelectric (ME) coupling is an inherent property of only a few crystals exhibiting very low coupling coefficients at low temperatures. On the other hand, these materials are desirable due to many promising applications, e.g. as efficient data storage devices or medical or geophysical sensors. Efficient coupling of magnetic and electric fields in materials can only be achieved in composite structures. Here, ferromagnetic (FM) and ferroelectric (FE) phases are combined e.g. including FM particles in a FE matrix or embedding fibers of the one phase into a matrix of the other. The ME coupling is then accomplished indirectly via strain fields exploiting magnetostrictive and piezoelectric effects. This requires a poling of the composite, where the structure is exposed to both large magnetic and electric fields. The efficiency of ME coupling will strongly depend on the poling process. Besides the alignment of local polarization and magnetization, it is going along with cracking, also being decisive for the coupling properties. Nonlinear ferroelectric and ferromagnetic constitutive equations have been developed and implemented within the framework of a multifield, two-scale FE approach. The models are microphysically motivated, accounting for domain and Bloch wall motions. A second, so called condensed approach is presented which doesn't require the implementation of a spatial discretisation scheme, however still considering grain interactions and residual stresses. A micromechanically motivated continuum damage model is established to simulate degradation processes. The goal of the simulation tools is to predict the different constitutive behaviors, ME coupling properties and lifetime of smart magnetoelectric devices.

  17. Choice of excitation source for determination of rare earth elements with radioisotope excited X ray fluorescence

    International Nuclear Information System (INIS)

    Zhang Quanshi; Chang Yongfu

    2000-01-01

    The comparisons of two radioisotope source ( 241 Am and 238 Pu) which are the most available in the radioisotope excited X Ray Fluorescence (XRF) analysis technique and two characteristic X ray series (KX and LX) analyzed for the determination of the rare-earth (RE) elements were investigated in detail. According to the principle of emission and detection of X ray , the relative excitation efficiencies were calculated by the some fundamental physical parameters including the photoelectric mass attenuation coefficient, the fluorescent yield, the absorption jump factor, the emission probability of the detected fluorescent line with reference to other liens of the same series etc., The advantages and disadvantages of the two conditions are discussed. These results may determine the optimal excitation and detection conditions for different rare-earth elements. The experimental results with nine rare-earth elements (Ce, Nd, Sm, Tb, Tm, Ho, Er, Yb and Lu) are in agreement with the results of theoretical calculations

  18. Gamma spectrometry at OSIRIS. Determination of the power and combustion rate of irradiated fuel elements

    International Nuclear Information System (INIS)

    Destot, M.; Musso, J.F.; Cerles, J.M.

    1975-12-01

    An original gamma spectrometer is available at Saclay near the core of the Osiris reactor. With such a device, it is possible to investigate nuclear fuel elements irradiated at Osiris or originating from power reactors. It is quite possible to build devices based on this principle in nuclear power reactors, more particularly in water reactors. With such a device, it is possible to follow the evolution in space and with time of a large number of fission products, and from there to draw precious conclusions relative to reactor safety (e.g. failed element detection) and to fuel economy (i.e. determination of combustion rate). The general characteristics of the device are given as well as its applications: determination of the mass combustion and of the linear power of an irradiated element. A non-destructive, versatile and fast means of investigation is therefore given by the installation of gamma spectroscopy inside a reactor [fr

  19. 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

  20. 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

  1. [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.

  2. Determination of essential elements in dietetic sample by neutron activation analysis

    International Nuclear Information System (INIS)

    Siquelli, Murilo V.; Maihara, Vera A. Maihara

    2005-01-01

    In the last years there has been an increase of the dietetic product consumption by people who suffer from diabetes, heart disease and by people concerned about having a healthy life as well. Despite the increase of dietetic product presents in the diet of the Brazilian population, the use of these products is still controversial. The analysis of the nutritional composition of these products is becoming important because a great number of people is changing their traditional food by dietetic products. In the literature, there is no information about the inorganic composition, mainly related to the essential elements, in the dietetic products: diet and light . In this study are presented preliminary results of the concentrations of Br, Ca, Cr, Fe, Na and Zn determined by Instrumental Neutron Activation Analysis in aspartame, saccharin and cyclamate sodium , and stevia based sweetener samples. Gelatin samples, diet and light, were also analyzed. Methodology validation was done analyzing NIST reference materials Tea Leaves (INCT-TL-1) and Mixed Polish Herbs (INCT-MPH-2). (author)

  3. What Level Design Elements Determine Flow? : How Light and Objects Guide the Player in Overwatch and Doom

    OpenAIRE

    Eliasson, David

    2017-01-01

    This thesis presents a comparative study between Overwatch (2016) and Doom (2016) to determine how these fast-paced games facilitate flow in their gameplay. The second chapter looks at formal definitions of flow and level design to establish a vocabulary for following chapters. Through formal analysis the level designs of both games are then examined to establish what elements in them guide players and keep the flow in gameplay. The thesis also examines how the initial gameplay design princip...

  4. 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

  5. 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.

  6. Characterization of airborne particulate matter in Santiago, Chile. Part 6: elemental determination by neutron activation analysis

    International Nuclear Information System (INIS)

    Cassorla, V.; Rojas, X.; Andonie, O.; Gras, N.

    1995-01-01

    Instrumental neutron activation analysis was used for the chemical characterization of airborne particulate matter from some locations in the city of Santiago, Chile. The following elements were determined: Al, As, Br, Ca, Cl, Co, Cu, Cr, Fe, Mn, Na, Sb, Sc, V y Zn. The accuracy of the experimental procedure was evaluated using a standard reference material. (author). 3 refs, 3 figs, 4 tabs

  7. 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)

  8. 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

  9. 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)

  10. 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 ...

  11. 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)

  12. Development of an approach for qualitative and quantitative analysis of trace elements present in canine breast tumors by energy dispersive X-ray fluorescence

    International Nuclear Information System (INIS)

    Cozer, Thamara C.; Conceicao, Andre L.C.; Paschuk, Sergei A.; Rocha, Anna S.S. da; Fagundes, Alana C.F.; Maciel, Karla F.R.; Pimentel, Gustavo R.O.; Badelli, Juliana C.

    2015-01-01

    Studies performed with canines indicate that one of the main neoplasia which affect these animals are the breast tumors, representing from 25% to 50% of all kinds of tumors. Moreover, half of them are classified as malignant. In this sense, recent researches on humans have been associated the presence of certain trace elements with the development of breast neoplasia in those individuals. Then, as the breast tissue composition in canines is very similar to the humans, it is expected the same behavior. In this direction, a very effective technique to identify and to determinate trace elements concentration is the EDXRF. However, studies on this area are scarce in the literature. Therefore, in this work it was developed an approach to quantify the main trace elements present into these tumors with high sensitivity. For this purpose, it was determined calibration curves of standards samples diluted in water, with concentrations of Ca, Fe, Cu and Zn, ranging from 400mg/kg to 35mg/kg, from 20mg/kg to 2mg/kg, from 10mg/kg to 1mg/kg and from 100mg/kg to 10mg/kg, respectively. All calibration curves were linearly fitted and on basis in this behavior it was determined the sensitivity of our approach to quantify the concentration of the trace elements mentioned above. In addition, it is important to mention that studies in this area are of great potential, because EDXRF represents a quickly practical and non-destructive alternative to quantify trace elements. (author)

  13. Development of an approach for qualitative and quantitative analysis of trace elements present in canine breast tumors by energy dispersive X-ray fluorescence

    Energy Technology Data Exchange (ETDEWEB)

    Cozer, Thamara C.; Conceicao, Andre L.C.; Paschuk, Sergei A.; Rocha, Anna S.S. da; Fagundes, Alana C.F.; Maciel, Karla F.R.; Pimentel, Gustavo R.O.; Badelli, Juliana C., E-mail: thamara.cozer@gmail.com, E-mail: alconceicao@utfpr.edu.br, E-mail: sergei@utfpr.edu.br, E-mail: anna@utfpr.edu.br, E-mail: alanacarolinef@gmail.com, E-mail: karla_rimanski@hotmail.com, E-mail: g_rop@hotmail.com, E-mail: jubadellin@gmail.com [Universidade Tecnologica Federal do Parana (UTFPR), Curitiba, PR (Brazil). Lab. de Espectroscopia de Raio-X

    2015-07-01

    Studies performed with canines indicate that one of the main neoplasia which affect these animals are the breast tumors, representing from 25% to 50% of all kinds of tumors. Moreover, half of them are classified as malignant. In this sense, recent researches on humans have been associated the presence of certain trace elements with the development of breast neoplasia in those individuals. Then, as the breast tissue composition in canines is very similar to the humans, it is expected the same behavior. In this direction, a very effective technique to identify and to determinate trace elements concentration is the EDXRF. However, studies on this area are scarce in the literature. Therefore, in this work it was developed an approach to quantify the main trace elements present into these tumors with high sensitivity. For this purpose, it was determined calibration curves of standards samples diluted in water, with concentrations of Ca, Fe, Cu and Zn, ranging from 400mg/kg to 35mg/kg, from 20mg/kg to 2mg/kg, from 10mg/kg to 1mg/kg and from 100mg/kg to 10mg/kg, respectively. All calibration curves were linearly fitted and on basis in this behavior it was determined the sensitivity of our approach to quantify the concentration of the trace elements mentioned above. In addition, it is important to mention that studies in this area are of great potential, because EDXRF represents a quickly practical and non-destructive alternative to quantify trace elements. (author)

  14. 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.)

  15. ICP OES Determination of Contaminant Elements Leached from Food Packaging Films

    Directory of Open Access Journals (Sweden)

    Éder José dos Santos

    2017-08-01

    Full Text Available ABSTRACT Determination of potential contaminants elements in food packing films arising from contact with acidic aqueous foods was undertaken by inductively coupled plasma optical emission spectrometry (ICP OES in accordance with DIN EN 1186-1. Test sections from plastic films were totally immersed in 3% w/v CH3COOH used as the food simulant. Testing was conducted under three conditions: (1 10 days at 40 ºC; (2 30 min at 70 ºC and 10 days at 40 ºC; and (3 30 min at 100 ºC and 10 days at 40 ºC. These time and temperature conditions were considered to be the most severe situations likely to be encountered in practice. Several different containers were investigated, including a borosilicate glass beaker, a glass bottle used for food canning, as well as one of polystyrene. The glass bottle was selected for testing treatments according to procedure (3 and a polystyrene one was chosen for use with procedures (1 and (2. Limits of quantitation were adequate for the determination of Ag, B, Ba, Cd, Cr, Cu, Pb, Sb, Sn and Zn by solution nebulization ICP OES and As by chemical vapor generation (CVG-ICP OES. Results for the analysis of AccuStandard certified reference materials as well as spike recoveries show good agreement with expected concentrations, demonstrating the accuracy and precision of the determinations. Eleven samples of food packing material were analyzed. The lead was present in the range 4.8 - 85.3 µg L-1 in 10 of 11 evaluated packing material, showing the importance of quality control measures.

  16. Levels of Essential Elements in Different Medicinal Plants Determined by Using Inductively Coupled Plasma Mass Spectrometry

    Directory of Open Access Journals (Sweden)

    Eid I. Brima

    2018-01-01

    Full Text Available The objective of this study was to investigate the content of essential elements in medicinal plants in the Kingdom of Saudi Arabia (KSA. Five different medical plants (mahareeb (Cymbopogon schoenanthus, sheeh (Artemisia vulgaris, harjal (Cynanchum argel delile, nabipoot (Equisetum arvense, and cafmariam (Vitex agnus-castus were collected from Madina city in the KSA. Five elements Fe, Mn, Zn, Cu, and Se were determined by using inductively coupled plasma mass spectrometry (ICP-MS. Fe levels were the highest and Se levels were the lowest in all plants. The range levels of all elements in all plants were as follows: Fe 193.4–1757.9, Mn 23.6–143.7, Zn 15.4–32.7, Se 0.13–0.92, and Cu 11.3–21.8 µg/g. Intakes of essential elements from the medical plants in infusion were calculated: Fe 4.6–13.4, Mn 6.7–123.2, Zn 7.0–42.7, Se 0.14–1.5, and Cu 1.5–5.0 µg/dose. The calculated intakes of essential elements for all plants did not exceed the daily intake set by the World Health Organization (WHO and European Food Safety Authority (EFSA. These medicinal plants may be useful sources of essential elements, which are vital for health.

  17. 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)

  18. 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

  19. k{sub 0}-INAA for determining chemical elements in bird feathers

    Energy Technology Data Exchange (ETDEWEB)

    Franca, Elvis J., E-mail: ejfranca@usp.b [CENA/USP, Centro de Energia Nuclear na Agricultura, Universidade of Sao Paulo, P.O. Box 97, 13400-970, Piracicaba, SP (Brazil); Fernandes, Elisabete A.N.; Fonseca, Felipe Y. [CENA/USP, Centro de Energia Nuclear na Agricultura, Universidade of Sao Paulo, P.O. Box 97, 13400-970, Piracicaba, SP (Brazil); Antunes, Alexsander Z. [IF, Instituto Florestal do Estado de Sao Paulo, Rua do Horto 931, Horto Florestal 02377-000, Sao Paulo, SP (Brazil); Bardini Junior, Claudiney; Bacchi, Marcio A.; Rodrigues, Vanessa S.; Cavalca, Isabel P.O. [CENA/USP, Centro de Energia Nuclear na Agricultura, Universidade of Sao Paulo, P.O. Box 97, 13400-970, Piracicaba, SP (Brazil)

    2010-10-11

    The k{sub 0}-method instrumental neutron activation analysis (k{sub 0}-INAA) was employed for determining chemical elements in bird feathers. A collection was obtained taking into account several bird species from wet ecosystems in diverse regions of Brazil. For comparison reason, feathers were actively sampled in a riparian forest from the Marins Stream, Piracicaba, Sao Paulo State, using mist nets specific for capturing birds. Biological certified reference materials were used for assessing the quality of analytical procedure. Quantification of chemical elements was performed using the k{sub 0}-INAA Quantu Software. Sixteen chemical elements, including macro and micronutrients, and trace elements, have been quantified in feathers, in which analytical uncertainties varied from 2% to 40% depending on the chemical element mass fraction. Results indicated high mass fractions of Br (max=7.9 mg kg{sup -1}), Co (max=0.47 mg kg{sup -1}), Cr (max=68 mg kg{sup -1}), Hg (max=2.79 mg kg{sup -1}), Sb (max=0.20 mg kg{sup -1}), Se (max=1.3 mg kg{sup -1}) and Zn (max=192 mg kg{sup -1}) in bird feathers, probably associated with the degree of pollution of the areas evaluated. In order to corroborate the use of k{sub 0}-INAA results in biomonitoring studies using avian community, different factor analysis methods were used to check chemical element source apportionment and locality clustering based on feather chemical composition.

  20. 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)

  1. Determination of element distributions between symplasm and apoplasm of cucumber plant parts

    International Nuclear Information System (INIS)

    Varga, A.; Zaray, G.; Fodor, F.

    2000-01-01

    Total reflection x-ray fluorescence analysis (TXRF) is a suitable method for determination of trace elements in biological samples due to its low detection limits, small sample demand, simple quantification and the absence of memory effects. In the present work the concentration of Pb, Cd, Ni, Mn and Fe was determined inside the cells (symplasm) and in the space among the cells (apoplasm) of cucumber plants. The cucumber seeds were grown in different nutrient solutions containing iron as Fe(III)-EDTA or Fe(III)-citrate, as well as Pb, Cd or Ni as contaminants in concentration of 10 -5 M. After growing period and the appropriate pretreatment (infiltration, leaching, washing and drying) the roots and the leaves were prepared for the analysis using a microwave assisted digestion system. The solutions obtained were spiked with Ni (in the case of the experiments with Pb) or Ga as internal standard. It was established that in the root the relative amount of lead in the symplasm related to the total absorbed amount (symplasm + apoplasm) is 2.5 % in presence of EDTA and 24% in presence of citrate. Studying its transport to the shoots, the amount of lead shows a decreasing tendency towards the young leaves and the symplasm/apoplasm ratio also changes: the ratio increased up to 66 % and 50 % in case of EDTA and citrate, respectively. Investigating of iron content similar phenomenon could be observed, however the presence of lead and complex forming agents did not result in any significant changes of the manganese distribution between symplasm and apoplasm. The results of experiments with Ni and Cd contaminants will be presented and discussed in the lecture. (author)

  2. 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)

  3. Multi-element determination in cancellous bone of human femoral head by PIXE

    International Nuclear Information System (INIS)

    Yuanxun Zhang; Yongping Zhang; Yongpeng Tong; Shijing Qiu; Xiaotao Wu; Kerong Dai

    1996-01-01

    Proton Induced X-ray Emission (PIXE) method is used for the determination of elemental concentrations in cancellous bone of human femoral head from five autopsies and seven patients with femoral neck broken. The specimen preparation and experimental procedure are described in detail. Using the t test, the results show that the concentrations of P, Ca, Fe, Cu, Sr in control group are higher than those in patient group, but the concentrations of S, K, Zn, Mn are not significantly different. The physiological functions of metallic elements in human bone are also discussed. (author). 19 refs., 1 fig., 4 tabs

  4. In situ quantitative determination of transuranic elements in areas of high-level gamma radiation

    International Nuclear Information System (INIS)

    Brodzinski, R.L.; Wogman, N.A.

    1978-01-01

    A technique is described for passive neutron monitoring of transuranic elements. The method provides quantitative determinations of transuranic element concentrations in a variety of field situations where no other measurement method is possible. The technique can measure concentrations of transuranic oxides as low as 8 nCi/cmsup 3 and is capable of operating in gamma radiation fields up to megarads per hour. Information on chemical and isotopic composition can also be obtained from the data. Several successful applications of the technique are discussed. 1 ref

  5. Finite Element Model of the Strain Gauge For Determining Uniaxial Tension

    Directory of Open Access Journals (Sweden)

    Vladimír GOGA

    2013-12-01

    Full Text Available Strain gauge is device used to measure the mechanical strains of solid bodies. Deformation of the strain gauge element causes changes its electrical resistance. This resistance change, usually measured using a Wheatstone bridge, is related to the strain by the quantity known as the gauge factor. When the stains are known, it is possible to determined state of stress at a point of measured body using generalized Hooke`s law and Mohr`s circle. Finite element analysis of strain gauge measurement using ANSYS software is subject of this article.

  6. Determination of elements in industrial waste sample and TENORM using XRF Technique in Nuclear Malaysia

    International Nuclear Information System (INIS)

    Paulus, W.; Sarimah Mahat; Meor Yusoff Meor Sulaiman

    2011-01-01

    Industrial waste such as aluminium dross and TENORM waste, oil sludge has been used as sample in this research. Determination of main elements by using X-Ray Fluorescence (XRF) in Material Technology Group, Malaysian Nuclear Agency. Results shows that main elements in these samples, aluminium and silicon, respectively. Thereby, this research shows that XRF can be considered as one of the techniques that can be used in waste characterization and furthermore, it can help researchers and engineer in the research related to waste treatment especially radioactive waste. (author)

  7. In situ quantitative determination of transuranic elements in areas of high-level gamma radiation

    International Nuclear Information System (INIS)

    Brodzinski, R.L.; Wogman, N.A.

    1978-01-01

    A technique is described for passive neutron monitoring of transuranic elements. The method provides quantitative determinations of transuranic element concentrations in a variety of field situations where no other measurement method is possible. The technique can measure concentrations of transuranic oxides as low as 8 nCi/cm 3 and is capable of operating in gamma radiation fields up to megarads per hour. Information on chemical and isotopic composition can also be obtained from the data. Several successful applications of the technique are discussed

  8. 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)

  9. Determination of two dimensional axisymmetric finite element model for reactor coolant piping nozzles

    International Nuclear Information System (INIS)

    Choi, S. N.; Kim, H. N.; Jang, K. S.; Kim, H. J.

    2000-01-01

    The purpose of this paper is to determine a two dimensional axisymmetric model through a comparative study between a three dimensional and an axisymmetric finite element analysis of the reactor coolant piping nozzle subject to internal pressure. The finite element analysis results show that the stress adopting the axisymmetric model with the radius of equivalent spherical vessel are well agree with that adopting the three dimensional model. The radii of equivalent spherical vessel are 3.5 times and 7.3 times of the radius of the reactor coolant piping for the safety injection nozzle and for the residual heat removal nozzle, respectively

  10. Determination of the element-specific complex permittivity using a soft x-ray phase modulator

    Science.gov (United States)

    Kubota, Y.; Hirata, Y.; Miyawaki, J.; Yamamoto, S.; Akai, H.; Hobara, R.; Yamamoto, Sh.; Yamamoto, K.; Someya, T.; Takubo, K.; Yokoyama, Y.; Araki, M.; Taguchi, M.; Harada, Y.; Wadati, H.; Tsunoda, M.; Kinjo, R.; Kagamihata, A.; Seike, T.; Takeuchi, M.; Tanaka, T.; Shin, S.; Matsuda, I.

    2017-12-01

    We report on directly determining the complex permittivity tensor using a method combining a developed light source from a segmented cross undulator of synchrotron radiation and the magneto-optical Kerr effect. The empirical permittivity, which carries the electronic and magnetic information of a material, has element specificity and has perfect confirmation using the quantum-mechanical calculation for itinerant electrons systems. These results help in understanding the interaction of light and matter, and they provide an interesting approach to seek the best materials as optical elements, for example, in extended-ultraviolet lithographic technologies or in state-of-the-art laser technologies.

  11. 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)

  12. Determination of toxic elements in foodstuffs from local market in Jakarta

    International Nuclear Information System (INIS)

    Surtipanti Sadjirun; Suwirma Safri; Endang Rosadi; Yumiarti; Yune Mellawati; Saifudin Simon; Minarni Ak

    1988-01-01

    The main foodstuffs of Indonesian people are, rice, bean, corn, wheat, vegetables, fruits, meat, fish, milk, tea, and coffee. The problem of the control of toxic elements in foodstuffs have not been carried out such as many countries, so there is no established maximum permissible concentration in the Indonesian national legislation, and that is why Indonesia participates in the Co-ordinated Research Program organized by the International Atomic Energy Agency. This program will allow exchange of experience among the participants, especially in the determination of low level toxic elements in foodstuffs using nuclear techniques. 6 refs, 9 tabs

  13. Investigations for chromatographic separation and determination of the rare earths and auxiliary group elements

    International Nuclear Information System (INIS)

    Post, K.

    1981-01-01

    Different method have been developed to quantitatively determine rare earth elements after their column chromatographic separation. The influence of the active solvents in the running systems diethyl ether/tetra hydrofuran (THF)/nitric acid (HNO 3 ) and diethyl ether/bis-(2-ethyl hexyl) phosphate (HDEHP)/HNO 3 was investigated on the column chromatographic separation of all rare earth elements is possible by the synergistic combination of the active running components THF and HDEHP. Further from product isotopes could also be separated using the running agents described here in investigations to separate fission product mixtures of irradiated uranium. (orig./HBR) [de

  14. Determination of impurity elements in steel by spark source mass spectrometry using powdered salts

    International Nuclear Information System (INIS)

    Saito, Morimasa; Sudo, Emiko

    1975-01-01

    Determination of impurity elements in steel by speak source mass spectrometry using powdered salts sample electrode was studied. The instrument used in this study was an AEI MS-7 mass spectrograph and the ion detector was Ilford Q2 photograph. Sample, (0.5--1) gram, was dissolved in hydrochloric acid (1 : 1) or nitric acid (1 : 1) together with yttrium of 1 microgram as the internal standard and then the solution was evaporated to dryness without baking. The salt residues were dried at 70 0 C for 30 minutes under vacuum. They were mixed with an equal amount of graphite powder for 5 minutes in a mixer mill, and then pressed into electrodes. When the relative sensitivity coefficient (Fe=1) was determined by using NBS 460 series standard samples, the results obtained by the proposed method for elements of Mo, Sn, Cu, Cr, Co, Ni, Mn, V, P, Si, and B were in good agreement with those obtained by the conventional method using solid sample electrodes (the solid method) and the precision of this method for 11 elements mentioned above was about 10% better than those of the solid method. However, both the accuracy and precision for elements of Nb, Ti, S and W were not good. This method was applied to the determination of impurities in NBS stainless steel and others. The relative standard deviations were within 20%. (auth.)

  15. 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

  16. 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)

  17. The complex variable boundary element method: Applications in determining approximative boundaries

    Science.gov (United States)

    Hromadka, T.V.

    1984-01-01

    The complex variable boundary element method (CVBEM) is used to determine approximation functions for boundary value problems of the Laplace equation such as occurs in potential theory. By determining an approximative boundary upon which the CVBEM approximator matches the desired constant (level curves) boundary conditions, the CVBEM is found to provide the exact solution throughout the interior of the transformed problem domain. Thus, the acceptability of the CVBEM approximation is determined by the closeness-of-fit of the approximative boundary to the study problem boundary. ?? 1984.

  18. Determination of burnup for IEAR-1 fuel elements by non destructive method of gamma spectrometry

    International Nuclear Information System (INIS)

    Madi Filho, T.; Holland, L.

    1982-01-01

    Burnup determination, by non-destructive gamma spectrometry of spent fuel with high and low activity of IEAR-1 reactor, using Cs-137 as burnup monitor, were done. To measure the Cs-137 distribution in these elements a Ge(Li) detector, with volume equal to 73,7 cm 3 , in two measurement systems with defined geometry and good colimation, was used. The IEA-14 taken from the core about 20 years ago, presents a gamma spectra due to Cs-137. The IEA-80, with cooling time approximately to 5 years, shows a more complex gamma spectrum due to other fission products still found in significant quantities. The IEA-14 measures were done in a measurement system used outside the reactor pool (S.I.), being the global efficiency of this system obtained by using a plane, calibrated and extense Ag-110 m source. Detailed measures of gamma transmission, using Cs-137 as a calibrated and punctiforme source, showed the high homogenity of the fuel plates. (E.G.) [pt

  19. 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

  20. 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

  1. [Determination of inorganic elements in different parts of Sonchus oleraceus L by flame atomic absorption spectrometry].

    Science.gov (United States)

    Wang, Nai-Xing; Cui, Xue-Gui; Du, Ai-Qin; Mao, Hong-Zhi

    2007-06-01

    Flame atomic absorption spectrometry with air-acetylene flame was used for the determination of inorganic metal elements in different parts ( flower, leaf, stem and root) of Sonchus oleraceus L. The contents of Ca, Mg, K, Na, Fe, Mn, Cu, Zn, Cr, Co, Ni, Pb and Cd in the flower, leaf, stem and root of Sonchus oleraceus L were compared. The order from high to low of the additive weight (microg x g(-1)) for the 13 kinds of metal elements is as follows: leaf (77 213.72) > flower (47 927.15) > stem(42 280.99) > root (28 131.18). From the experimental results it was found that there were considerable differences in the contents of the metal elements in different parts, and there were richer contents of Fe, Zn, Mn and Cu in root and flower, which are necessary to human health, than in other parts.

  2. Determination of rare earth elements in rice by INAA and ICP-MS

    International Nuclear Information System (INIS)

    Pham Thi Huynh, M.; Chu Pham Ngoc, S.; Carrot, F.; Revel, G.; Dang Vu, M.

    1997-01-01

    Irrigation of rice plants with a solution of rare earth elements increases both the production capacity and the resistance to disease. Assuming that the treated plants remain expendable, the different parts of plants, root stalk and grain, were analyzed by instrumental neutron activation analysis (INAA) and by mass spectrometry after plasma excitation (ICP-MS). About 40 elements were determined. The results showed that the contamination remained in the roots and was absent in rice grains. The analytical distribution of different elements in different parts of both treated and non-treated plants has given some information concerning the possible effect of the rare earth treatment. The performances of the two analytical methods have been compared. (author)

  3. Determination of the minimum number of fuel elements of the RP-10 research reactor

    International Nuclear Information System (INIS)

    Languasco, J.

    1989-01-01

    The peruvian research reactor RP-10 is composed of a compound nucleus of boxes containing fuel plates which are cooled with light water in order to remove heat produced by fission of uranium atoms. However from a certainty viewpoint, it exists certain restrictions to design the cooling system. The most admissible caloric flux of 90.3 watts/cm 2 is deflux of 90.3 watts/cm 2 is determined on the basis of these thermic restrictions when cooling speed is 409 cm/sec permitting at least 24 fuel elements(boxes) within the nucleus. On the basis of restrictions of load loss in the nucleus, it would be permitted at least 18 fuel elements, but this quantity breaks thermic restrictions for this reason, 24 boxes in the nucleus will be the minimum number of elements

  4. The determination of lanthanum and lanthanide elements by means of X-ray fluorescence analysis

    International Nuclear Information System (INIS)

    Kuelcue, N.

    1982-01-01

    The quantitative analysis of all lanthanide elements (except Pm) was carried out concurrently using X-ray fluorescence analysis. By choice of suitable preparative methods (thin layer samples prepared by pipetting solutions onto filter paper) and use of an internal standard (Sr) it was possible to obtain linear calibration curves up to high concentrations in the solution (85 g/l) and to suppress disturbances caused by absorption and secondary fluorescence. A correction procedure was developed for reflection superimpositions in the L-spectra of the lanthanide elements which, through selection of the most favourable reflections for analysis, permitted concurrent determination of all 14 elements. Main and secondary constitutents can be analysed whereas enrichment is required for trace analysis. Under routine usage the actual limits of detection range from 3 to 17 μg/cm 2 or alternatively 0.3 to 1.7 mg/ml. (orig.) [de

  5. 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)

  6. 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.

  7. Determination of radionuclides and elemental composition of clay soils by gamma and X-ray spectrometry

    International Nuclear Information System (INIS)

    Isinkaye, O. M.; Shitta, O. M. B.; Oderinde, O. M.

    2011-01-01

    Radiochemical and elemental analysis of clay soils collected from different locations within Ekiti State have been performed in this study using gamma and XRF spectrometric measurements. The results of this study show that the mean concentration of 238 U ranged from 2.2±1.0ppm to 3.2±1.1ppm, 232 Th ranged from 4.0±0.5ppm to 5.7±1.7ppm, while 40 K presented in percent by weight ranged from 0.4±0.2 to 1.3±0.3. The XRF analysis revealed 4 major elements and 11 minor or trace elements present in the clay samples. The distribution of the various major and trace elements in all the sampling sites do not follow any systematic trend but vary from point to point. To assess the level of contamination and the possible anthropogenic impact in the clay soils, the enrichment factor (EF) and the geoaccumulation index (Igeo) were estimated for some potential hazardous elements. The results indicate that Cu, Zn, Ni and Mn have EF<2 indicating minimal or no enrichment while Pb is moderately enriched in all the locations.

  8. Experimental parameters optimization of instrumental neutron activation analysis in order to determine selected elements in some industrial soils in Turkey

    International Nuclear Information System (INIS)

    Haciyakupoglu, Sevilay; Nur Esen, Ayse; Erenturk, Sema

    2014-01-01

    The purpose of this study is optimization of the experimental parameters for analysis of soil matrix by instrumental neutron activation analysis and quantitative determination of barium, cerium, lanthanum, rubidium, scandium and thorium in soil samples collected from industrialized urban areas near Istanbul. Samples were irradiated in TRIGA MARK II Research Reactor of Istanbul Technical University. Two types of reference materials were used to check the accuracy of the applied method. The achieved results were found to be in compliance with certified values of the reference materials. The calculated E n numbers for mentioned elements were found to be less than 1. The presented data of element concentrations in soil samples will help to trace the pollution as an impact of urbanization and industrialization, as well as providing database for future studies. - Highlights: • Optimization of experimental parameters is important for high sensitivity results by INAA. • Assessment of uncertainty sources is necessary to increase reliability of results. • The aim of this study is to determine a number of elements in industrial soil samples. • The higher concentrations of studied elements are due to rapid industrialization. • This baseline data can be used in future studies for other industrial areas

  9. 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)

  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. 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.)

  12. 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)

  13. Determination of essential and toxic elements in clay soil commonly consumed by pregnant women in Tanzania

    Science.gov (United States)

    Mwalongo, D.; Mohammed, N. K.

    2013-10-01

    A habit of eating clay soil especially among pregnant women is a common practice in Tanzania. This practice known as geophagy might introduce toxic elements in the consumer's body to endanger the health of the mother and her child. Therefore it is very important to have information on the elemental composition of the eaten soil so as to assess the safety nature of the habit. In this study 100 samples of clay soil, which were reported to be originating from five regions in Tanzania and are consumed by pregnant women were analyzed to determine their levels of essential and toxic elements. The analysis was carried out using energy dispersive X-ray fluorescent technique (EDXRF) of Tanzania Atomic Energy Commission, Arusha. Essential elements Fe, Zn, Cu, Se and Mn and toxic elements As, Pb, Co, Ni, U and Th were detected in concentrations above WHO permissible limits in some of the samples. The results from this study show that the habit of eating soil is exposing the pregnant mothers and their children to metal toxicity which is detrimental to their health. Hence, further actions should be taken to discourage the habit of eating soil at all levels.

  14. Determination of elemental in soil samples from Gebeng area using NAA technique

    International Nuclear Information System (INIS)

    Md Suhaimi Elias; Wo, Y.M.; Mohd Suhaimi Hamzah

    2016-01-01

    Rapid development and urbanization will increase number of residence and industrial area. Without proper management and control of pollution, these will give an adverse effect to environment and human life. The objective of this study to identify and quantify key contaminants into the environment of the Gebeng area as a result of industrial and human activities. Gebeng area was gazetted as one of the industrial estate in Pahang state. Assessment of elemental pollution in soil of Gebeng area base on level of concentration, enrichment factor and geo-accumulation index. The enrichment factors (EFs) were determined by the elemental rationing method, whilst the geo-accumulation index (I_g_e_o) by comparing of current to continental crustal average concentration of element. Twenty-seven of soil samples were collected from Gebeng area. Soil samples were analysed by using Neutron Activation Analyses (NAA) technique. The obtained data showed higher concentration of iron (Fe) due to abundance in soil compared to other elements. The results of enrichment factor showed that Gebeng area have enrich with elements of As, Br, Hf, Sb, Th and U. Base on the geo-accumulation index (I_g_e_o) classification, the soil quality of Gebeng area can be classified as class 0, (uncontaminated) to Class 3, (moderately to heavily contaminated). (author)

  15. Determination of major elements in annual tree rings by acid extraction

    International Nuclear Information System (INIS)

    Belacy, N.; Abou EL-Nour, F.; Simpson, H.J.

    1991-01-01

    A method utilizing acid extraction of Na, K, Ca and Mg from the wood of annual growth rings of egyptian trees was executed. The method was applied on a Morus Alba tree located at Nile delta, northern of egypt. The acid extraction method includes the use of dilute nitric acid to extract the elements of the wood. The wood was soaked for one hour with continuous stirring at room temperature. Element contents of both leachant and ash of the extracted wood dissolved in 2N HNO 3 , were then estimated using an atomic absorption spectrophotometer. The method was optimized and led to an accurate determination of the elements in the wood of the examined tree rings. The results showed a difference in the level of these elements along the annual rings of the examined tree. The data obtained in this work can help in understanding the correlation between the concentration of these elements in the annual growth rings of the egyptian trees and the expected changes in the salinity of water of irrigation before and after the high dam project

  16. Determination of Major and Minor Elements in the Code River Sediments

    International Nuclear Information System (INIS)

    Sri Murniasih; Sukirno; Bambang Irianto

    2007-01-01

    Analyze major and minor elements in the Code river sediments has been done. The aim of this research is to determine the concentration of major and minor elements in the Code river sediments from upstream to downstream. The instrument used were X-ray Fluorescence using Si(Li) detector. The results show that major elements were Fe (1.66 ± 0.1% - 4.20 ± 0.7%) and Ca (4.43 ± 0.6% - 9.08 ± 1.3%); while minor elements were Ba (178.791 ± 21.1 ppm - 616.56 ± 59.4 ppm); Sr (148.22 ± 21.9 ppm - 410.25 ± 30.5 ppm); and Zr (9.71 ± 1.1 ppm - 22.11 ± 3.4 ppm). ANAVA method (confidence level of α 0.05 ) for statistic test was used. It was showed that there were significant influence of the sampling location difference on the concentration of major and minor elements in the sediment samples. (author)

  17. Determination of the stability limit of a thermoacoustic engine by means of finite elements

    NARCIS (Netherlands)

    de Jong, Anne; Wijnant, Ysbrand H.; de Boer, Andries

    2013-01-01

    A finite element model is presented to obtain the stability limit of, as an example, 2D standing wave thermoacoustic engine. The stability limit is the required heating to obtain self-sustained (thermo)acoustic oscillations. The method used to obtain the stability limit is not restricted to the

  18. Determination of sixteen elements and arsenic species in brown, polished and milled rice.

    Science.gov (United States)

    Narukawa, Tomohiro; Matsumoto, Eri; Nishimura, Tsutomu; Hioki, Akiharu

    2014-01-01

    The concentrations of 16 elements in 10 rice flour samples and the distribution of the elements in the rice grains from which the flour were made were determined by ICP-MS and ICP-OES after microwave-assisted digestion of the samples. Arsenic speciation analysis was carried out by HPLC-ICP-MS following heat-assisted extraction of the sample. The concentrations of inorganic As (As(III) and As(V)), monomethylarsonic acid (MMAA) and dimethylarsinic acid (DMAA) and their distribution in the rice grains were determined. Portions of the brown rice were polished/milled to different degrees to yield milled off samples and polished rice samples. All samples were powdered and analyzed for 16 elements and for As species. The recoveries and mass balances for all elements in all samples showed good agreements with the starting materials. As(III), As(V), MMAA and DMAA were detected, and the sums of the concentrations of all species in the extract were 86-105% of the total As concentration in each case.

  19. Determination of 21 elements by INAA for certification of SRM 1570a, Spinach

    International Nuclear Information System (INIS)

    Becker, D.A.

    1995-01-01

    Analyses for certification have been made by instrumental neutron activation analysis (INAA) for the determination of 21 elements in the National Institute of Standards and technology (NIST) Spinach renewal reference material, SRM 1570a. Elements determined included ones with short halflife products (Al, V, Ca, Mg) intermediate halflife products (Mn, Na, K, La), and long halflife products (Ba, Co, Cr, Cs, Eu, Fe, Rb, Sb, Sc, Se, Sr, Th, and Zn). For the first time a new robotic sample changer was used in the counting of long halflife indicator isotopes for certification of an SRM. Uncertainties obtained averaged ± 1.80% for the four major and minor constituents (Ca, K, Mg, Na); ± 3.14% for elements with concentrations form 1 to 400 mg/kg (Al, Ba, Cr, Fe, Mn, Rb, Sr, and Zn); and ± 8.31% for the ultra trace elements (<1 mg/kg) (Co, Cs, Eu, La, Sb, Sc, Se, Th, and V). (author) 3 refs.; 3 tabs

  20. 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

  1. Determination of urine metabolites containing radioactivatable elements by molecular neutron activation analysis

    International Nuclear Information System (INIS)

    Blotcky, A.J.; Rack, E.P.

    1986-01-01

    As urine is a final stage for the metabolic pathways of essential trace elements or chemical toxins, it is becoming increasingly important to not only report levels of trace elements but to determine the molecular or ionic identity of these trace elements. For a biological system such as urine, a molecular neutron activation analysis (MONAA) approach must involve a deproteinization step, where necessary, to ensure that metabolites such as amino acids, bases, r nucleosides are not protein bound prior to chemical separation. This can involve the simple application of ammonia or acid hydrolysis. All separations for the metabolites containing the radioactivatable element must be performed prior to neutron irradiation and subsequent radioassay for the metabolite. Separation procedures can include high-pressure liquid chromotography (HPLC), ion-exchange chromatography, size exclusion chromatography, solvent extraction, and/or gas chromatography. After separation, the separated metabolite is neutron irradiated and and radioassayed for the radioactivity in the metabolite. A review of previous work involving the determination of hormonal iodine, iodoamino acids, chlorinated pesticides, trimethyl-selenonium, and selenoamino acids in urine is discussed

  2. 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)

  3. 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.

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

    International Nuclear Information System (INIS)

    Prohaska, K.

    2003-02-01

    Sequential and simultaneous atomic spectrometric detection was applied for the determination of metals in human whole blood, blood fractions and joint tissues. For this purpose ICP-OES (inductively coupled plasma - optical emission spectrometry) and GFAAS (graphite furnace - atomic absorption spectrometry) were optimized. The nebulizing technique of the ICP-OES causes a high consumption of the sample (2.4 mL /min uptake rate). Using the simultaneous modus of measurement it is possible to determine up to 20 elements in the samples of interest. Using GFAAS the elements can be detected sequentially only, the method is more time consuming in comparison. For the direct sample injection into the graphite tube only 20 aeL are needed. Since 1 mL sample has to be filled in the sample vessel of the autosampler, up to six elements can be determined in this volume. The most important advantage of the simultaneous multi-element detection is the low sample consumption, which is essential for analysis of biological samples. Normally only small amounts of human blood or tissues can be collected, and the concentrations of analytes are usually very low. Therefore in many cases a sample preparation is of advantage, which enables a pre-concentration of the analyte. The sample digestion was optimized with respect to the possible pre-concentration of the analytes. Ashing of the freeze-dried blood enabled a six fold higher concentration in the measuring solution compared with wet digestion of blood. For the ICP-OES sample introduction system two different nebulizers were tested in the complex matrix of the digested blood samples. A Meinhard and the microconcentric nebulizer were compared according to their analytical performance. The matrix of the samples caused LODs three to five times higher than in the aqueous standards. The application of the Meinhard nebulizer enabled sufficiently low LODs in the matrix for some elements of interest (Ca, Cu, Fe, Mg, P, S, Zn in freeze-dried blood

  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. 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)

  7. 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.)

  8. 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)

  9. 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)

  10. 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

  11. 12 CFR 997.4 - Calculation of the quarterly present-value determination.

    Science.gov (United States)

    2010-01-01

    ... 12 Banks and Banking 7 2010-01-01 2010-01-01 false Calculation of the quarterly present-value determination. 997.4 Section 997.4 Banks and Banking FEDERAL HOUSING FINANCE BOARD NON-BANK SYSTEM ENTITIES RESOLUTION FUNDING CORPORATION OBLIGATIONS OF THE BANKS § 997.4 Calculation of the quarterly present-value...

  12. 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

  13. 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)

  14. Role of NAA in determination and characterisation of sampling behaviours of multiple elements in CRMs

    International Nuclear Information System (INIS)

    Tian Weizhi; Ni Bangfa; Wang Pingsheng; Nie Huiling

    2002-01-01

    Taking the advantage of high precision and accuracy of neutron activation analysis (NAA), sampling constants have been determined for multielements in several international and Chinese reference materials. The suggested technique may be used for finding elements in existing CRMs qualified for quality control (QC) of small size samples (several mg or less), and characterizing sampling behaviors of multielements in new CRMs specifically made for QC of microanalysis. (author)

  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. 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...

  17. 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.)

  18. 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

  19. 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

  20. Distribution of copper and other elements in ryegrass roots, determined with a scanning proton microprobe

    International Nuclear Information System (INIS)

    Mazzolini, A.P.; Legge, G.J.F.

    1982-01-01

    A scanning proton microprobe has been used to determine the distribution of Cu and other elements in Wimmera ryegrass roots grown in solution cultures. Cu was found to be localized on or near the surface of the roots in randomly distributed discrete zones. The distribution of Cu was partially correlated with those of Fe, P and Ca and possibly indicates some form of association; co-precipitation in a precipitate of ferric phosphate or hydroxy-oxide is favoured

  1. 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

  2. Application of activation analysis for determination of some elements in cassiterite samples; Aplicacao da analise por ativacao para a determinacao de alguns elementos em amostras de cassiterita

    Energy Technology Data Exchange (ETDEWEB)

    Armelin, Maria Jose Aguirre

    1978-07-01

    This work consists in the development of an analytical method using activation by thermal neutrons for the determination of some minor elements and traces present in cassiterite (tin ore). This method was then applied to determine these elements in samples of cassiterite from different regions of Brazil. An analysis was made of the mineralogy characteristic of cassiterite as well as of the minerals most commonly associated with it. Four main types of interference were found to occur in the analysis by activation of trace elements in samples of cassiterite. The method involves the analysis without chemical separation for the determination of some elements and the analysis with chemical separation for the determination of other elements. The steps involved in both types of analysis are described. In the analysis with chemical separation the matrix element (tin) is separated by distillation in an H{sub 2}SO{sub 4}-HBr medium, after fusion of the ore with Na{sub 2}O{sub 2}. Arsine and antimony are determined in the distilled, whereas some lanthanide elements and uranium are determined in the distillation residue by separating them as a group by precipitation with lanthanum fluoride. A discussion on the precision, accuracy and sensibility of the method is also included. (author)

  3. Elemental identification of blue paintings traces present in historic cemeteries in the São Martinho region, southern Brazil

    Science.gov (United States)

    Costa, Thiago G.; Richter, Fábio Andreas; Castro, Elisiana Trilha; Gonçalves, Samantha; Spudeit, Daniel A.; Micke, Gustavo A.

    2018-03-01

    Cemeteries are of great significance in many communities, often being considered of invaluable historical, artistic, architectural and cultural significance and thus they need to be preserved. In this regard, understanding the historical aspects and the construction techniques used is essential for their protection. The purpose of this paper is to describe historical aspects of the funerary heritage present in the region of São Martinho in southern Brazil, along with an analysis of the blue paint found in cemeteries of German colonies in the region studied. FTIR analysis suggests that the binder is composed mostly of a protein resin and a small amount of lipid. The morphology of the pigment was investigated by SEM and EDS and the spectra revealed that the major elements present in the blue pigment are Na, Al, Si and S, with an overlap in the elemental mapping, indicative of ultramarine pigments. The GC-MS results are consistent with the type of binder identified by FTIR and indicate a mixture of oils, probably from vegetal sources, and proteins.

  4. Improvement in the determination of elemental concentrations in PIXE analyses using artificial neural system

    International Nuclear Information System (INIS)

    Correa, R.; Dinator, M.I.; Morales, J.R.; Miranda, P.A.; Cancino, S.A.; Vila, I.; Requena, I.

    2008-01-01

    An Artificial Neural System, ANS, has been designed to operate in the analysis of spectra obtained from a PIXE (Proton Induced X-ray Emissions) application. The special designed ANS was used in the calculation of the concentrations of the major elements in the samples. Neural systems using several feed-forward ANN of similar topology working in parallel were trained with error back propagation algorithm using sets of spectra of known elemental concentrations. Following the training phase of the neural networks, other PIXE spectra were analyzed with this methodology providing unknown elemental concentrations. ANS results were compared with results obtained by traditional computer codes like AXIL and GUPIX, obtaining correlations factors close to one. The rather short time required to process each spectrum, of the order of microseconds, allows fast analysis of a large number of samples. Here we present applications of ANS in the PIXE analyses of samples of organic nature like liver, gills and muscle from fishes. ANS results were compared with elemental concentrations obtained in a previous application where a single ANN was used for each analyzed element. PIXE analyses were performed at the Nuclear Physics Laboratory of the University of Chile, using 2.2 MeV proton beams provided by a Van de Graaff accelerator. (author)

  5. 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.)

  6. Determination of essential and toxic elements in clay soil commonly consumed by pregnant women in Tanzania

    International Nuclear Information System (INIS)

    Mwalongo, D.; Mohammed, N.K.

    2013-01-01

    A habit of eating clay soil especially among pregnant women is a common practice in Tanzania. This practice known as geophagy might introduce toxic elements in the consumer's body to endanger the health of the mother and her child. Therefore it is very important to have information on the elemental composition of the eaten soil so as to assess the safety nature of the habit. In this study 100 samples of clay soil, which were reported to be originating from five regions in Tanzania and are consumed by pregnant women were analyzed to determine their levels of essential and toxic elements. The analysis was carried out using energy dispersive X-ray fluorescent technique (EDXRF) of Tanzania Atomic Energy Commission, Arusha. Essential elements Fe, Zn, Cu, Se and Mn and toxic elements As, Pb, Co, Ni, U and Th were detected in concentrations above WHO permissible limits in some of the samples. The results from this study show that the habit of eating soil is exposing the pregnant mothers and their children to metal toxicity which is detrimental to their health. Hence, further actions should be taken to discourage the habit of eating soil at all levels. - Highlights: • We assessed exposure of heavy metals to pregnant mothers who consume geophagic soil. • We analyzed 100 samples of soil originated in Tanzania. • The technique used was energy dispersive X-ray fluorescent. • Essential and toxic elements were detected in concentrations above WHO limits. • Hence, geophagy is exposing pregnant mothers and their children to metal toxicity

  7. Exploring the uncertainty in attributing sediment contributions in fingerprinting studies due to uncertainty in determining element concentrations in source areas.

    Science.gov (United States)

    Gomez, Jose Alfonso; Owens, Phillip N.; Koiter, Alex J.; Lobb, David

    2016-04-01

    One of the major sources of uncertainty in attributing sediment sources in fingerprinting studies is the uncertainty in determining the concentrations of the elements used in the mixing model due to the variability of the concentrations of these elements in the source materials (e.g., Kraushaar et al., 2015). The uncertainty in determining the "true" concentration of a given element in each one of the source areas depends on several factors, among them the spatial variability of that element, the sampling procedure and sampling density. Researchers have limited control over these factors, and usually sampling density tends to be sparse, limited by time and the resources available. Monte Carlo analysis has been used regularly in fingerprinting studies to explore the probable solutions within the measured variability of the elements in the source areas, providing an appraisal of the probability of the different solutions (e.g., Collins et al., 2012). This problem can be considered analogous to the propagation of uncertainty in hydrologic models due to uncertainty in the determination of the values of the model parameters, and there are many examples of Monte Carlo analysis of this uncertainty (e.g., Freeze, 1980; Gómez et al., 2001). Some of these model analyses rely on the simulation of "virtual" situations that were calibrated from parameter values found in the literature, with the purpose of providing insight about the response of the model to different configurations of input parameters. This approach - evaluating the answer for a "virtual" problem whose solution could be known in advance - might be useful in evaluating the propagation of uncertainty in mixing models in sediment fingerprinting studies. In this communication, we present the preliminary results of an on-going study evaluating the effect of variability of element concentrations in source materials, sampling density, and the number of elements included in the mixing models. For this study a virtual

  8. Determination of chemical elements in africanized Apis mellifera (Hymenoptera: Apidae honey samples from the State of Piauí, Brazil

    Directory of Open Access Journals (Sweden)

    Geni da Silva Sodré

    2007-08-01

    Full Text Available Honey is a food used since the most remote times, appreciated for its characteristic flavor, considerable nutritional value and medicinal properties; however, little information exists about the presence of chemical elements in it. The objectives of this work were to determine the chemical elements present in 38 honey samples, collected directly from beekeepers from the State of Piauí, Brazil and to verify whether they presented any contamination. The chemical elements were determined by means of Total Reflection X-ray Fluorescence. The means of three replicates were: K (109.671 ± 17.487, Ca (14.471 ± 3.8797, Ti (0.112 ± 0.07, Cr (0.196 ± 0.11, Mn (0.493 ± 0.103, Fe (1.722 ± 0.446, Co (0.038, Ni (0.728 ± 0.706, Cu (0.179 ± 0.0471, Zn (0.967 ± 0.653, Se (not detected, Br (not detected, Rb (0.371 ± 0.097, Sr (0.145 ± 0.45, Ba (11.681, Hg (not detected, and Pb (0.863 µg g-1.

  9. X-Ray fluorescence determination of the mobile forms of toxic elements in meadow chernozems

    International Nuclear Information System (INIS)

    Belikov, K.N.; Blank, A.B.; Shevtsov, N.I.

    1997-01-01

    An X-ray fluorescence method for determining mobile forms of Mn, V, Cr, Co, Ni, Zn, and Pb in meadow chernozems was developed. It is based on the extraction of analytes with an acetate-ammonia buffer solution and the evaporation of the obtained filtrate with carbon powder followed by the X-ray fluorescence analysis of the dry residue. The effect of concomitants on the analytical signals of elements under determination was examined. It was suggested to spike samples with barium in order to decrease analytical errors. (author)

  10. Determining the degree of grafting for poly (vinylidene fluoride) graft-copolymers using fluorine elemental analysis

    International Nuclear Information System (INIS)

    Yu Yang; Zhang Bowu; Yang Xuanxuan; Deng Bo; Li Linfan; Yu Ming; Li Jingye

    2011-01-01

    Acrylic acid (AAc) and styrene (St) were grafted onto poly (vinylidene fluoride) (PVDF) powder or membrane samples by pre-irradiation graft copolymerization. The grafted chains were proved by FT-IR spectroscopy analysis. The degree of grafting (DG) of the grafted PVDF was determined by fluorine elemental analysis (FEA) method, and was compared with the DGs determined by weighing method, acid-base back titration method and quantitative FT-IR method. The results show that the FEA method is accurate, convenient and universal, especially for the grafted polymer powders. (authors)

  11. [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.

  12. Determination of rare earth elements in rocks by neutron activation analysis with pre-irradiation separation

    International Nuclear Information System (INIS)

    Alcala, A.L.

    1991-01-01

    Rare earth elements were determined by neutron activation analysis in rocks, a group separation before irradiation was developed. The international reference standards AGV-1, BE-N and JB-1, as well the Brazilian geological standards BB-1 and GB-1, provided by the Instituto de Geociencias da Universidade Federal da Bahia, were analysed. The method was based on acid digestion of the samples, cation exchange separation, and coprecipitation of the REE with calcium oxalate. Interferents like U, Th, Ta and Fe were eliminated. The concentration values of eleven REE's (La, Co, Pr, Nd, Sm, Eu, Gd, Tb, Ho, Yb and Lu) were determined. (author)

  13. Complexometric determination of rare earth elements in quartz glasses with indicator xylenol orange-cetylpyridinium chloride

    International Nuclear Information System (INIS)

    Svistunova, G.P.; Amelin, V.G.

    1988-01-01

    A study was made on possibility of using the system xylenol orange (XO)-cetypyridinium determination of REE. XO forms with REE in the presence of CP intensively coloured complexes with absorbtion maximums at 610-615 nm. Colour transformation from blue to yellow is observed during complexometric titration in CP presence in the final point of titration by EDTA solution. The method was applied for Eu and Ce determination in alloyed quartz glasses. Titanium doesn't prevent REE determination at its content in titrated solution up to 1 mg. Other elements affect slightly the results. The method is recommended to use for 0.1-0.7% REE determination in quartz glasses of 0.5-1.5 g samples

  14. Complexometric determination of rare earth elements in quartz glasses with indicator xylenol orange-cetylpyridinium chloride

    Energy Technology Data Exchange (ETDEWEB)

    Svistunova, G P; Amelin, V G

    1988-11-01

    A study was made on possibility of using the system xylenol orange (XO)-cetypyridinium determination of REE. XO forms with REE in the presence of CP intensively coloured complexes with absorbtion maximums at 610-615 nm. Colour transformation from blue to yellow is observed during complexometric titration in CP presence in the final point of titration by EDTA solution. The method was applied for Eu and Ce determination in alloyed quartz glasses. Titanium doesn't prevent REE determination at its content in titrated solution up to 1 mg. Other elements affect slightly the results. The method is recommended to use for 0.1-0.7% REE determination in quartz glasses of 0.5-1.5 g samples.

  15. Determinant representations of spin-operator matrix elements in the XX spin chain and their applications

    Science.gov (United States)

    Wu, Ning

    2018-01-01

    For the one-dimensional spin-1/2 XX model with either periodic or open boundary conditions, it is shown by using a fermionic approach that the matrix element of the spin operator Sj- (Sj-Sj'+ ) between two eigenstates with numbers of excitations n and n +1 (n and n ) can be expressed as the determinant of an appropriate (n +1 )×(n +1 ) matrix whose entries involve the coefficients of the canonical transformations diagonalizing the model. In the special case of a homogeneous periodic XX chain, the matrix element of Sj- reduces to a variant of the Cauchy determinant that can be evaluated analytically to yield a factorized expression. The obtained compact representations of these matrix elements are then applied to two physical scenarios: (i) Nonlinear optical response of molecular aggregates, for which the determinant representation of the transition dipole matrix elements between eigenstates provides a convenient way to calculate the third-order nonlinear responses for aggregates from small to large sizes compared with the optical wavelength; and (ii) real-time dynamics of an interacting Dicke model consisting of a single bosonic mode coupled to a one-dimensional XX spin bath. In this setup, full quantum calculation up to N ≤16 spins for vanishing intrabath coupling shows that the decay of the reduced bosonic occupation number approaches a finite plateau value (in the long-time limit) that depends on the ratio between the number of excitations and the total number of spins. Our results can find useful applications in various "system-bath" systems, with the system part inhomogeneously coupled to an interacting XX chain.

  16. 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)

  17. 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

  18. Experimental determination of chosen document elements parameters from raster graphics sources

    Directory of Open Access Journals (Sweden)

    Jiří Rybička

    2010-01-01

    Full Text Available Visual appearance of documents and their formal quality is considered to be as important as the content quality. Formal and typographical quality of documents can be evaluated by an automated system that processes raster images of documents. A document is described by a formal model that treats a page as an object and also as a set of elements, whereas page elements include text and graphic object. All elements are described by their parameters depending on elements’ type. For future evaluation, mainly text objects are important. This paper describes the experimental determination of chosen document elements parameters from raster images. Techniques for image processing are used, where an image is represented as a matrix of dots and parameter values are extracted. Algorithms for parameter extraction from raster images were designed and were aimed mainly at typographical parameters like indentation, alignment, font size or spacing. Algorithms were tested on a set of 100 images of paragraphs or pages and provide very good results. Extracted parameters can be directly used for typographical quality evaluation.

  19. 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

  20. 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. 

  1. 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)

  2. [Determination of 10 elements in the feather of brown-eared pheasant by ICP and AAS].

    Science.gov (United States)

    Wu, Yu-Zhen; Zhang, Feng; Wang, Meng-Ben; Zhao, Gen-Gui

    2008-03-01

    Crossoptilon mantchuricum (brown-eared pheasant) is an endemic to northern China and one of the state first-protection animals, which is now confined to scattered localities in Guandi Mountains, Guancen Mountains, Luliang Ranges of western Shanxi, and the mountains of north-western Hebei, western Beijing and central Shaanxi. Its range is fragmented by habitat loss because of human activity and other intervention, and isolated populations are resulting in facing the extinction risk from further forest destroyed and other pressures. The trace elements are very important to the growth and development of brown-eared pheasant, and these elements in the feather are closely correlated to the contents in the organs of the bird. By research on the elements contents in the feather, the authors are able to get more information about the growth, development, reproduction, immunity and metabolism function for this bird. The aim of this study is to try providing scientific basis for further enhancing the protection and the artificial breeding. Ten elements including Mo, Zn, Ni, Fe, Mn, Cr, Cu, K, Pb and Cd were determined in the feather of brown-eared pheasant by ICP and AAS, respectively. For the analysis two samples were from Luya Mountain Natural Reserve and Pangquangou Natural Reserve, and one was from Taiyuan Zoo, Shanxi. The contents of the elements in the feather of wild and captive brown-eared pheasants were compared each other. The results showed that the contents of the eight elements the feather from the Zoo were lower than those from Luya Mountain Natural Reserve and Pangquangou Natural Reserve. Moreover, Fe is the highest among those ten elements, Cd was not found, and Mo and Cr were much lower than the others. It is suggested that varying habitats have obvious effects on the elements contents of wild bird body, and wild habitant is more beneficial to the bird growth and development. Applying the results to wild animal management would be favorable to the protection

  3. 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

    Neutron Activation analysis (NAA) is a multi element analysis technique, often non-destructive in nature where approximately 75 elements can be measured with the detection limits ranging from 10 -6 to 10 -12 g of element in a sample. Typical sample sizes range from 1 mg to 1 g, however in principle much larger samples can be activated and the size is only limited by the capacity of the neutron irradiation facility. In NAA, a sample (solid or liquid or gas) is exposed to neutrons and radiations emitted by the radioactive products, formed during the nuclear reaction, are measured using a suitable detector. The energy of the emitted radiation is a characteristic of a radioisotope whereas the intensity of the emitted radiation is proportional to the mass of the analyte. NAA can be carried out by measurement of (i) prompt gamma rays emitted by compound nucleus, called prompt gamma ray NAA (PGNAA) and (ii) β rays emitted from radioactive product or delayed gamma rays emitted subsequent to β decay, called conventional NAA or simply NAA. PGNAA is an online measurement method. PGNAA is complementary to conventional NAA in terms of analyzing low Z elements. Conventional NAA is an offline method and is easy to perform. Depending upon the nature of matrix and analyte to be determined, three approaches are possible in NAA namely, (i) instrumental neutron activation analysis (INAA), (ii) radiochemical neutron activation analysis (RNAA), and (iii) chemical neutron activation analysis (CNAA). Quantification is accomplished by any of the three standardisation methodologies namely (i) absolute method (ii) relative method and (iii) single comparator method. The relative method is most precise and simple to perform. Natural processes responsible for the formation of bottom sediments can be altered by anthropogenic activities. Bottom sediments are a sink as well as a source of contaminants in the aquatic environment. Analysis of-sediments provides environmentally significant

  4. Methods for determining the carrying capacity of eccentrically compressed concrete elements

    Directory of Open Access Journals (Sweden)

    Starishko Ivan Nikolaevich

    2014-04-01

    Full Text Available The author presents the results of calculations of eccentrically compressed elements in the ultimate limit state of bearing capacity, taking into account all possiblestresses in the longitudinal reinforcement from the R to the R , caused by different values of eccentricity longitudinal force. The method of calculation is based on the simultaneous solution of the equilibrium equations of the longitudinal forces and internal forces with the equilibrium equations of bending moments in the ultimate limit state of the normal sections. Simultaneous solution of these equations, as well as additional equations, reflecting the stress-strain limit state elements, leads to the solution of a cubic equation with respect to height of uncracked concrete, or with respect to the carrying capacity. According to the author it is a significant advantage over the existing methods, in which the equilibrium equations using longitudinal forces obtained one value of the height, and the equilibrium equations of bending moments - another. Theoretical studies of the author, in this article and the reasons to calculate specific examples showed that a decrease in the eccentricity of the longitudinal force in the limiting state of eccentrically compressed concrete elements height uncracked concrete height increases, the tension in the longitudinal reinforcement area gradually (not abruptly goes from a state of tension compression, and load-bearing capacity of elements it increases, which is also confirmed by the experimental results. Designed journalist calculations of eccentrically compressed elements for 4 cases of eccentric compression, instead of 2 - as set out in the regulations, fully cover the entire spectrum of possible cases of the stress-strain limit state elements that comply with the European standards for reinforced concrete, in particular Eurocode 2 (2003.

  5. Essential and toxic element determination in edible mushrooms by neutron activation analysis

    International Nuclear Information System (INIS)

    Moura, Patricia Landim da Costa

    2008-01-01

    In this study concentrations of As, Br, Co, Cr, Cs, Fe, K, Na, Rb, Se and Zn were determined in edible mushrooms acquired from commercial establishments in the city of Sao Paulo and directly from Mogi das Cruzes, Suzano, Juquitiba and Mirandopolis producers. The analytical technique used for determining these elements in edible mushrooms was Instrumental Neutron Activation Analysis (INAA). Species of the Agaricus, Lentinus and Pleurotus genera were acquired during the period from November, 2006 to March, 2007. About 150 to 200 mg of freeze-dried mushrooms were irradiated in a neutron flux of 1012 cm -2 s -1 for 8 hours in the IEA-R1 nuclear research reactor at IPEN-CNEN-SP. In order to evaluate the precision and accuracy of the methodology, four reference materials: INCT-MPH-2 Mixed Polish Herbs and INCT-TL-1 Tea Leaves, NIST SRM 1577b Bovine Liver, and the material Mushroom from IAEA were analyzed. Results showed some variation in the element concentrations among the different genera. In some samples, arsenic was found but in low concentrations. Arsenic is probably derived from the contamination from pesticides used in the cultivation, in their the substrates where mushrooms uptake their nutrients. Although there are element concentration variations, mushrooms can still be considered a very rich nutritional source, mainly because of their low concentrations of Na, and due to the good source of K, Fe and Zn. (author)

  6. Determination of essential elements in commercial infant foods by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Vallinoto, Priscila; Maihara, Vera A.

    2013-01-01

    Eating habits are important determinants of health conditions during childhood. Commercial infant food is an important part of the diet for many babies. As such it is necessary that such food contain sufficient amounts of essential elements. Inadequate complementary feeding is a major cause of high rates of malnutrition throughout the world. Commercial infant food is classified into four different stages: Stages 1 and 2 are adequate for babies older than 6 months, but new flavors and food are introduced in stage 2; Stage 3 is offered to 8 month old babies; Junior Stage is recommended to children over 1 year old. In this study, essential elements: Ca, Cl, Co, Cr, Fe K, Mg, Mn, Na, Se and Zn were determined in commercial infant food samples by Instrumental Neutron Activation Analysis (INAA). Twenty-seven infant food samples were bought in stores around Sao Paulo city during 2011. These samples were freeze-dried and homogenized before analysis. The powdered samples were irradiated in the IEA-R1 nuclear research reactor of IPEN-CNEN/SP. For validation of the methodology, INCT MPH-2 Mixed Polish Herbs and NIST-SRM 1577b Bovine Liver reference materials were analyzed. Most of the concentration results were below the World Health Organization's recommended daily intake for infants from 6 to 12 months old. These low essential element concentration results in commercial infant foods obtained in our study indicate that infants should not only be fed with commercial baby foods. (author)

  7. Determination of essential elements in commercial infant foods by instrumental neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Vallinoto, Priscila; Maihara, Vera A., E-mail: pvallinoto@ipen.br, E-mail: vmaihara@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    Eating habits are important determinants of health conditions during childhood. Commercial infant food is an important part of the diet for many babies. As such it is necessary that such food contain sufficient amounts of essential elements. Inadequate complementary feeding is a major cause of high rates of malnutrition throughout the world. Commercial infant food is classified into four different stages: Stages 1 and 2 are adequate for babies older than 6 months, but new flavors and food are introduced in stage 2; Stage 3 is offered to 8 month old babies; Junior Stage is recommended to children over 1 year old. In this study, essential elements: Ca, Cl, Co, Cr, Fe K, Mg, Mn, Na, Se and Zn were determined in commercial infant food samples by Instrumental Neutron Activation Analysis (INAA). Twenty-seven infant food samples were bought in stores around Sao Paulo city during 2011. These samples were freeze-dried and homogenized before analysis. The powdered samples were irradiated in the IEA-R1 nuclear research reactor of IPEN-CNEN/SP. For validation of the methodology, INCT MPH-2 Mixed Polish Herbs and NIST-SRM 1577b Bovine Liver reference materials were analyzed. Most of the concentration results were below the World Health Organization's recommended daily intake for infants from 6 to 12 months old. These low essential element concentration results in commercial infant foods obtained in our study indicate that infants should not only be fed with commercial baby foods. (author)

  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. Iron Quadrangle, Brazil. Elemental concentration determined by k0-instrumental neutron activation analysis. Part 2. Kale samples

    International Nuclear Information System (INIS)

    Menezes, M.A.B.C.; Palmieri, H.E.L.; Leonel, L.V.; Nalini, H.A.Jr.; Jacimovic, R.

    2006-01-01

    The objective of this study was to evaluate the influence of mining activity on elemental concentrations in kale grown around a mining area. Two sites studied are in the Iron Quadrangle, Minas Gerais, Brazil, considered one of the richest mineral-bearing regions in the world. One site is near mineral exploration activity and the other is an ecological area. A comparator site outside the Iron Quadrangle was also analyzed. This work focused on the determination of the elemental concentrations in kale applying the k 0 -instrumental neutron activation analysis. As the Brazilian legislation specifies values for soil only, the results for kale were compared to the literature values and it was found that the vegetable does not present any health risks. (author)

  10. Determination of element composition by means of neutron activation analysis in vitro

    International Nuclear Information System (INIS)

    Zedgenidze, G.A.; Brovtsyn, V.K.; Spryshkova, R.A.; Porokhov, S.N.; Borisov, G.I.; Leonov, V.F.

    1979-01-01

    A method of neutron activation analysis of bones in vitro for calcium, phosphorus, sodium, chlorine and magnesium with the use of reactor neutrons was proposed. The normal osseous tissue was the object of studies. Samples obtained from diaphyses of the femur, tibia, fibula and also from distal epiphysis of the femur, proximal epiphysis of the tibia and fibula were analysed. Osseous tissue samples were taken from 17 male cadavers aged 20-52. The mean indices of the concentration of the elements in the diaphyses and epiphyses of bones in various age groups, averaged values of concentrations for the entire age range and also the weighted mean content of these elements according to age groups were determined

  11. 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

  12. 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)

  13. 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)

  14. Spectroscopic determination of essential elements in unpolished rice (oryza sativa l.), grown at rri, Dokri

    International Nuclear Information System (INIS)

    Shar, G.Q.; Arain, S.A.; Shar, L.A.; Kazi, T.G.; Sahito, S.

    2005-01-01

    seven rice varieties collected from, Rice Research institute (RRI) Dokri, Sindh in Pakistan. Agricultural soil samples was also collected to evaluate the bioavailability of eight essential elements to seven varieties of rice grown in the same agricultural plot. The agricultural soil and rice varieties were digested by wet acid digestion method. Homogeneity of the prepared materials was evaluated through the determination of eight essential elements i.e., Na, K, Mg, Ca, Fe, Mn, Zn, using flame atomic absorption spectrophotometer. The unpolished rice varieties contained high amount of essential micro nutrients such as Na, K, Mg, Ca, Fe, Mn, Zn, and Cu (616.01, 4097.15, 626.20, 73.90, 1829.88, 50.34, 42.72 and 7.21 mg/kg) in seven different varieties of rice i.e. DR-82, DR83, DR92, Kanwal-95, Lateefi, Sadahayat and Sarshar respectively. (author)

  15. Rare earth elements determination in medicinal plants by Neutron Activation Analisys

    International Nuclear Information System (INIS)

    Goncalves, Rodolfo D.M.R.; Francisconi, Lucilaine S.; Silva, Paulo S.C. da

    2013-01-01

    Rare Earth Elements (REEs) have been considered nontoxic for human health and for the environment; however, the use of REEs in the development of recent technologies has increased the interest un their biological effects. Some studies related to their concentration in foodstuffs were published but REEs levels in medicinal plants are still unknown. The objective of this study was to determine the Rees concentration in the set of 59 medicinal herbs commonly used by Brazilian folk. Results showed that plants can concentrate REEs in their aerial parts, but the amount transferred to the extract of these plants is relatively low, resulting in little ingestion of these elements by the population during the extract consumption. (author)

  16. Determination of Rare Earth Elements in Thai Monazite by Inductively Coupled Plasma and Nuclear Analytical techniques

    International Nuclear Information System (INIS)

    Busamongkol, Arporn; Ratanapra, Dusadee; Sukharn, Sumalee; Laoharojanaphand, Sirinart

    2003-10-01

    The inductively coupled plasma atomic emission spectroscopy (ICP-AES) for the determination of individual rare-earth elements (REE) was evaluated by comparison with instrumental neutron activation analysis (INAA) and x-ray fluorescence spectrometry (XRF). The accuracy and precision of INAA and ICP-AES were evaluated by using standard reference material IGS-36, a monazite concentrate. For INAA, the results were close to the certified value while ICP-AES were in good agreement except for some low concentration rare earth. The techniques were applied for the analysis of some rare earth elements in two Thai monazite samples preparing as the in-house reference material for the Rare Earth Research and Development Center, Chemistry Division, Office of Atoms for Peace. The analytical results obtained by these techniques were in good agreement with each other

  17. Rare earth elements determination in medicinal plants by Neutron Activation Analisys

    Energy Technology Data Exchange (ETDEWEB)

    Goncalves, Rodolfo D.M.R.; Francisconi, Lucilaine S.; Silva, Paulo S.C. da, E-mail: rdmrg89@usp.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    Rare Earth Elements (REEs) have been considered nontoxic for human health and for the environment; however, the use of REEs in the development of recent technologies has increased the interest un their biological effects. Some studies related to their concentration in foodstuffs were published but REEs levels in medicinal plants are still unknown. The objective of this study was to determine the Rees concentration in the set of 59 medicinal herbs commonly used by Brazilian folk. Results showed that plants can concentrate REEs in their aerial parts, but the amount transferred to the extract of these plants is relatively low, resulting in little ingestion of these elements by the population during the extract consumption. (author)

  18. Determination of individual rare earth elements in Vietnamese monazite by radiochemical neutron activation analysis

    International Nuclear Information System (INIS)

    Nguyen Van Suc; Nguyen Mong Sinh

    1993-01-01

    Radiochemical neutron activation analysis (RNAA) has been applied for determination of rare earth elements (REE) in Vietnamese monazite. The chemical separation procedure used is based on the chromatographic elution of rare earth groups, after the separation of 233 Pa(Th) in irradiated monazite samples by coprecipitation with MnO 2 , the rare earth elements were retained by Biorad AG1 x 8 resin column in 10% 15.4M HNO 3 -90% methanol solution. The elution of heavy rare earth (HREE) and middle rare earth (MREE) groups was carried out with 10% 1M HNO 3 - 90% methanol and 10% 0.05M HNO 3 -90% methanol solution, respectively; while the light rare earths (LREE) were eluted from the column by 0.1M HNO 3 solution. The accuracy of the method was checked by the analysis of granodiorite GSP-I and the rare earth values were in good agreement. (author) 7 refs.; 3 tabs

  19. Migration of components from cork stoppers to food: challenges in determining inorganic elements in food simulants.

    Science.gov (United States)

    Corona, T; Iglesias, M; Anticó, E

    2014-06-18

    The inorganic elements potentially migrating from cork to a food simulant [a hydroalcoholic solution containing 12 and 20% (v/v) ethanol] have been determined by means of inductively coupled plasma (ICP) with atomic emission and mass spectrometric detection. The experimental instrumental conditions were evaluated in depth, taking into account spectroscopic and nonspectroscopic interference caused by the presence of ethanol and other components in the sample. We report concentrations ranging from 4 μg kg(-1) for Cd to 28000 μg kg(-1) for Al in the food simulant (concentrations given in kilograms of cork). The values found for Ba, Mn, Fe, Cu, and Zn have been compared with the guideline values stated in EU Regulation 10/2011. In all cases, cork met the general safety criteria applicable to food contact material. Finally, we have proposed water as an alternative to the hydroalcoholic solution to simplify quantification of the tested elements using ICP techniques.

  20. Substoichiometric IDA in determination of zinc present in some spices (Paper No. RA-14)

    Energy Technology Data Exchange (ETDEWEB)

    Vaidya, M M; Ray, M N

    1982-01-01

    Results of separation and determination of zinc present in four spices, viz. Coriander, King's cumin, Fennel and Fenugreek seeds by IDA are presented. It is observed that zinc could be estimated by substoichiometric extraction as dithiozonate followed by IDA, in spices. The substoichiometric extraction results at lower concentrations of zinc also, but better results are obtained by increasing the concentration of zinc. The substoichiometric IDA agrees fairly with the conventional chemical analysis.

  1. 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

  2. Determination of pollutant elements and heavy metals in petroleum sludge and scale at Heglig field Sudan

    International Nuclear Information System (INIS)

    Amir, N. T.

    2012-02-01

    The release of pollutant metals from petroleum industry in to ecosystems represents a serious hazard for the biosphere, because of their toxicity. The objective of this study was to determine the levels of some elements in petroleum sludge and scales collected from petroleum production area in Heglig oil field located in South Kordofan State. The concentration of Ca, Fe, V, Mn,Ni, Cu, Zn, Cs, Sr, Zr, Y and Pb in sludge and scale samples have been determined using energy dispersive x-ray fluorescence (EDXRF) equipped with a point source of 1 09C d. The concentration of Ca and Fe in scale samples were found to fall in range of 15,49-23.28% and 0.98-5.13%, respectively. The a verge elemental concentrations of Ti, Mn, Ni, Cu, Zn, Sr,Y, and Pb in scale samples were 2917.8, 567.74, 23.21, 23.05, 101.67, 31.38, 177.06 and 24.12 (mg/kg), respectively. The concentrations of Ca and Fe in sludge samples ranged from 1.98-8.82% and 0.71-5.19%, respectively and the a verge elemental concentrations of Cs, V, Mn,Cu, Zn, Pb, Sr, Y and Zr were 7.44, 92,59, 557.36, 7.67, 162.72,28.67, 65.02, 45.64 and 52.15 (mg/kg), respectively. Correlation analysis revealed lock of any significant correlation between elemental concentrations in sludge and scales. (Author)

  3. Determination of selected toxic elements in leaves of White Hawthorn grown in a remote area

    Directory of Open Access Journals (Sweden)

    Zeiner M.

    2013-04-01

    Full Text Available One important plant of the Rosaceae family which is commonly used as phytopharmaceutical in Europe and North America is Hawthorn (Crataegus monogyna. The fruits, the leaves together with their extracts are applied in patients suffering mild cardiac disorders or nervosity. Since the leaves as well as the berries act as diuretics a sufficient micronutrient supply has to be guaranteed. On the other the quantities of toxic elements present in the plant parts should be at levels without harmful effects on human health. For this purpose Hawthorn leaves and flowers were collected in a remote area in 2011 and 2012 and analysed for their elemental composition. The metals uptaken from the soil were supposed to be in a similar range, thus the impact of airborne contamination by heavy metal translocation could be studied. The elements investigated were Ba, Cd, Co, Cr, Cu, Mn, Ni, Pb, Sr, and Zn. After harvesting the samples were dried, homogenized, digested and then analysed by ICP-AES. The contents of all elements are in the μg/g range. In the samples of 2012 higher concentrations were found for Co, Cu, Mn, Ni, and Zn, lower concentrations were registered for Ba, Pb, and Sr. The amounts of Cd and Cr were statistically insignificantly lower in 2012 than 2011.

  4. Multi-element determinations of N,N-dimethylformamide (DMF) coal slurries using ICP-OES

    Energy Technology Data Exchange (ETDEWEB)

    M. Mujuru; R.I. McCrindle; B.M. Botha; P.P. Ndibewu [Tshwane University of Technology, Pretoria (South Africa). Department of Chemistry

    2009-04-15

    A slurry nebulisation technique was applied for elemental analysis of bituminous coals SARM 18, SARM 19 and four coals from three different seams in Witbank, South Africa, by inductively coupled plasma optical emission spectroscopy (ICP-OES). Major elements (Al, Ca, Fe, Mg, S, Si and Ti) and trace elements (Ba, Cr, Mn, Ni, Sr, V, Zn and Zr) in coal were determined. Various slurry preparations were evaluated using two dispersants (glycerol and Triton X-100) and by varying the concentration of dispersants, between 0.1% and 1.0% (v/v). The effect of initially solubilising the ground coal in N,N-dimethylformamide (DMF) was investigated by varying the volume of DMF added. The effect of wet grinding with DMF was investigated. Wet grinding with DMF was shown to drastically reduce particle sizes (50.0% < 0.28 m and 90.0% < 6.17 {mu}m) as compared to dry grinding (50.0% < 5.25 {mu}m and 90.0% < 11.1 {mu}m). The reduced particle sizes and increased transport efficiency of the coal slurries led to improved analytical recoveries of elements in the reference coal, SARM 18. The best analytical recoveries for all elements were achieved using 0.1% Triton X-100 with 10.0% DMF. Results obtained by ICP-OES after wet grinding of the coal with DMF, using 0.1% Triton X-100, also gave excellent recoveries (Al, 100%; Ca, 103%; Cr, 106%; Fe, 102%; Mg, 100%; Mn, 104%; Ni, 109%; Si, 102%; Ti, 95.0%; and V, 108%). The results obtained with 10.0% DMF and 0.1% Triton X-100 were in agreement with certified values for all selected elements according to paired t-test at the 95.0% confidence level. Selected elements (Al, Ca, Fe, Mg, Mn, Si, Ti and V) were also analysed with X-ray fluorescence for comparison with results obtained from ICP-OES. Analysis by ICP-OES of microwave digested coal was also carried out. It is suggested that the DMF slurry technique could be used for routine analysis of bituminous coals. 27 refs., 4 figs., 4 tabs.

  5. Multielement determination and speciation of major-to-ultratrace elements in green tea leaves by ICP-AES and ICP-MS

    International Nuclear Information System (INIS)

    Matsuura, Hirotaka; Hokura, Akiko; Haraguchi, Hiroki

    2000-01-01

    In order to investigate the multi-elemental composition of green tea leaves as well as chemical species in tea infusions, inductively coupled plasma atomic emission spectrometry (ICP-AES) and inductively coupled plasma mass spectrometry (ICP-MS) were used for elemental analysis and elemental speciation with the aid of size exclusion chromatography (SEC). As a result, the multielement determination of major-to-ultratrace elements in green tea leaves and green tea infusions was carried out by ICP-AES and ICP-MS. About 40 elements in these tea samples could be determined in a wide concentration range of over 8 orders of magnitude. The extraction efficiency of each element was estimated as the ratio of its concentration in tea infusion to that in tea leaves. It was found from the experimental results that the elements in tea leaves could be classified into three characteristic groups, depending on their extraction efficiencies. Furthermore, tea infusions were analyzed by a combined system of SEC, UV absorption detector, and ICP-AES (or ICP-MS) for the speciation of major-to-ultratrace elements. Most of the elements in tea infusions were found to be present as associated complexes with large organic molecules. (author)

  6. Determination of Fluorine and other light elements in Syrian teeth by PIGE and PIXE techniques

    International Nuclear Information System (INIS)

    Bakraji, E.; Ahmad, M.; Doueer, M.

    2013-01-01

    The aim of this study is to determine the concentration of Fluorine in Syrian teeth collected from Southern and Coastal regions where both populations have almost similar dietary habits and similar occupational activities. The conventional PIGE method is used to determine Fluorine concentration in human teeth since its play an important role in bony and dental tissues, the low levels of Fluorine can play positive role against teeth cariosity and an inhibitor against certain enzyme systems, where high levels can cause dental Fluorosis and bone abnormalities for the bone structure. Several cations and anions have been studied in the drinking water of studied areas in order to investigate the role played by these elements and whether fluoridation within the normal levels of worldwide standard grading. Na, Mg, P and Ca concentrations have been determined in studied samples in order to compare with earlier works. (author)

  7. Utilization of atomic emission spectroscopy methods for determination of rare earth elements

    International Nuclear Information System (INIS)

    Kubova, J.; Polakovicova, J.; Medved, J.; Stresko, V.

    1997-01-01

    The authors elaborated and applied procedures for rare earth elements (REE) determination using optical emission spectrograph with D.C arc excitation and ICP atomic emission spectrometry.Some of these analytical method are described. The proposed procedure was applied for the analysis of different types of geological materials from several Slovak localities. The results the REE determination were used for e.g. investigation of REE distribution in volcanic rocks, rhyolite tuffs with uranium-molybdenum mineralization, sandstones with heavy minerals accumulations, phosphatic sandstones, granites, quartz-carbonate veins and in the meteorite found in the locality Rumanova. The REE contents were determined in 19 mineral water sources and the results obtained by the both mentioned methods compared. The total REE contents in the analysed mineral water samples were between 2 · 10 -7 and 3 · 10 -5 g dm -3

  8. 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.

  9. 26 CFR 1.430(h)(2)-1 - Interest rates used to determine present value.

    Science.gov (United States)

    2010-04-01

    ... 26 Internal Revenue 5 2010-04-01 2010-04-01 false Interest rates used to determine present value... to the interest rates to be applied for a plan year under section 430(h)(2). Section 430(h)(2) and... defined in section 414(f)). Paragraph (b) of this section describes how the segment interest rates are...

  10. 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

  11. 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

  12. Determination of multi-element profiles of soil using energy dispersive X-ray fluorescence (EDXRF)

    International Nuclear Information System (INIS)

    Yu, K.N.; Yeung, Z.L.L.; Lee, L.Y.L.; Stokes, M.J.; Kwok, R.C.W.

    2002-01-01

    The source profile for soil in Hong Kong is important both for determination of the main air pollutant source in Hong Kong and for assessment of the impact of Asian dust storms on Hong Kong. Soil associated with different rock types have been sampled, and the concentrations of 19 chemical elements, Na, Al, Si, Ti, V, Cr, Mn, Fe, Co, K, Ca, Ni, Cu, Zn, Pb, Rb, Sr, Y and Zr, have been determined using energy dispersive X-ray fluorescence. A profile for the average soil for Hong Kong has been determined by taking average values for the different soil categories. The values for the Hong Kong soil are commensurate with values for rural soil derived by other workers, except that Hong Kong soil has much lower Fe and Ca concentrations. The abundance of Al, Ca and Fe in the average Hong Kong soil are 9.23%, 0.11% and 0.85%. We conclude that Ca provides a good marker element for identifying dust episodes in Hong Kong while Al does not

  13. Determination of elemental tissue composition following proton treatment using positron emission tomography

    International Nuclear Information System (INIS)

    Cho, Jongmin; Ibbott, Geoffrey; Gillin, Michael; Gonzalez-Lepera, Carlos; Min, Chul Hee; Zhu, Xuping; El Fakhri, Georges; Paganetti, Harald; Mawlawi, Osama

    2013-01-01

    Positron emission tomography (PET) has been suggested as an imaging technique for in vivo proton dose and range verification after proton induced-tissue activation. During proton treatment, irradiated tissue is activated and decays while emitting positrons. In this paper, we assessed the feasibility of using PET imaging after proton treatment to determine tissue elemental composition by evaluating the resultant composite decay curve of activated tissue. A phantom consisting of sections composed of different combinations of 1 H, 12 C, 14 N, and 16 O was irradiated using a pristine Bragg peak and a 6 cm spread-out Bragg-peak (SOBP) proton beam. The beam ranges defined at 90% distal dose were 10 cm; the delivered dose was 1.6 Gy for the near monoenergetic beam and 2 Gy for the SOBP beam. After irradiation, activated phantom decay was measured using an in-room PET scanner for 30 min in list mode. Decay curves from the activated 12 C and 16 O sections were first decomposed into multiple simple exponential decay curves, each curve corresponding to a constituent radioisotope, using a least-squares method. The relative radioisotope fractions from each section were determined. These fractions were used to guide the decay curve decomposition from the section consisting mainly of 12 C + 16 O and calculate the relative elemental composition of 12 C and 16 O. A Monte Carlo simulation was also used to determine the elemental composition of the 12 C + 16 O section. The calculated compositions of the 12 C + 16 O section using both approaches (PET and Monte Carlo) were compared with the true known phantom composition. Finally, two patients were imaged using an in-room PET scanner after proton therapy of the head. Their PET data and the technique described above were used to construct elemental composition ( 12 C and 16 O) maps that corresponded to the proton-activated regions. We compared the 12 C and 16 O compositions of seven ROIs that corresponded to the vitreous humor, adipose

  14. 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)

  15. 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)

  16. 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)

  17. 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

  18. 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.

  19. Low-level determination of transuranic elements in marine environment samples

    International Nuclear Information System (INIS)

    Ballestra, S.; Holm, E.; Fukai, R.

    1978-01-01

    The procedures developed and currently employed in the Monaco Laboratory for determining transuranic elements in seawater, marine sediments and organisms are described and discussed. While the standard anion-exchange procedure from the hydrochloric acid medium is used for the separation of plutonium isotopes from americium, purification of americium and curium is achieved by an ion-exchange sorption from the methanol-nitric acid medium, followed by an elution with the methanol-hydrochloric acid mixture. Satisfactory clean-up of plutonium as well as americium and curium can be achieved by applying the described procedures. (author)

  20. 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)

  1. Determination of the concentration profile of chemical elements in superheater pipes

    International Nuclear Information System (INIS)

    Aldape U, F.; Aspiazu F, J.

    1986-05-01

    This work has for object to determine the profile of concentration of chemical elements at trace level in a superheater pipe of Thermoelectric Plants using the X-ray emission spectroscopy technique induced by protons coming from the Accelerator of the Nuclear Center. In the X-ray detection, a Si Li detector was used. The technique was chosen because it allows a multielemental analysis, of high sensitivity and precision. The results can help to understand the problems that are had in the change of flexibility or of corrosion. This will be from utility to the Federal Electricity Commission (CFE). (Author)

  2. 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

  3. 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

  4. Determination of elemental composition of metals using ambient organic mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Shiea, Christopher [Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, 100 Shih-Chuan 1st Rd, Kaohsiung 807, Taiwan (China); Huang, Yeou-Lih [Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, 100 Shih-Chuan 1st Rd, Kaohsiung 807, Taiwan (China); Department of Chemistry, National Sun Yat-Sen University, 70 Lien-Hai Rd, Kaohsiung 804, Taiwan (China); Cheng, Sy-Chyi; Chen, Yi-Lun [Department of Chemistry, National Sun Yat-Sen University, 70 Lien-Hai Rd, Kaohsiung 804, Taiwan (China); Shiea, Jentaie, E-mail: jetea@mail.nsysu.edu.tw [Department of Chemistry, National Sun Yat-Sen University, 70 Lien-Hai Rd, Kaohsiung 804, Taiwan (China); Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, 100 Shih-Chuan 1st Rd, Kaohsiung 807, Taiwan (China)

    2017-05-22

    Conventional inorganic mass spectrometric (MS) analysis of metals can require time-consuming and tedious sample preparation. We thus report the novel and direct characterization of metals in solid samples using an organic MS technique known as electrospray laser desorption ionization mass spectrometry (ELDI/MS). No sample pretreatment was needed, and results were rapidly obtained due to the ambient and laser-based nature of ELDI/MS. Metals from samples were desorbed and ionized by laser irradiation, after which they reacted with EDTA and then post-ionized and detected as metal-EDTA complexes. Aluminum, copper, iron, lead, nickel, and zinc from plates, foils, and coins were characterized in seconds. This study demonstrates that an ESI/MS system can be easily modified to analyze metal elements in solids by involving a chelating agent, indicating a potentially promising development in MS towards the analysis of metals using organic MS. - Highlights: • “Organic MS” was utilized as “inorganic MS” to detect metal ions in solid samples. • Element ions desorbed by laser irradiation rapidly reacted with a chelating reagent before they were detected by MS. • Elemental composition of metals was determined by this “Organic MS” method.

  5. Determination of elemental composition of metals using ambient organic mass spectrometry

    International Nuclear Information System (INIS)

    Shiea, Christopher; Huang, Yeou-Lih; Cheng, Sy-Chyi; Chen, Yi-Lun; Shiea, Jentaie

    2017-01-01

    Conventional inorganic mass spectrometric (MS) analysis of metals can require time-consuming and tedious sample preparation. We thus report the novel and direct characterization of metals in solid samples using an organic MS technique known as electrospray laser desorption ionization mass spectrometry (ELDI/MS). No sample pretreatment was needed, and results were rapidly obtained due to the ambient and laser-based nature of ELDI/MS. Metals from samples were desorbed and ionized by laser irradiation, after which they reacted with EDTA and then post-ionized and detected as metal-EDTA complexes. Aluminum, copper, iron, lead, nickel, and zinc from plates, foils, and coins were characterized in seconds. This study demonstrates that an ESI/MS system can be easily modified to analyze metal elements in solids by involving a chelating agent, indicating a potentially promising development in MS towards the analysis of metals using organic MS. - Highlights: • “Organic MS” was utilized as “inorganic MS” to detect metal ions in solid samples. • Element ions desorbed by laser irradiation rapidly reacted with a chelating reagent before they were detected by MS. • Elemental composition of metals was determined by this “Organic MS” method.

  6. Use of Hg-Electroplated-Pt Ultramicroelectrode for Determining Elemental Sulphur in Naphtha Samples

    Directory of Open Access Journals (Sweden)

    Carlos Eduardo de Andrade

    2012-01-01

    Full Text Available This paper describes the applicability of a Hg-electroplated-Pt ultramicroelectrode in the quantification of elemental sulphur in naphtha samples by square-wave voltammetry. A reproducible deposition methodology was studied and is reported in this paper. This methodology is innovative and relies on the quality of the mercury stock solution to obtain reproducible surfaces required for the analytical methodology. All analyses were performed using a Hg-electroplated-Pt ultramicroelectrode (Hg-Pt UME due to the low sensibility of such devices to ohmic drops in resistive solutions. The responses of the peak areas in voltammetric experiments were linear in all of the range studied. The method developed here is accurate and reproducible, with a detection limit of 0.010 mg L−1 and a good recovery range for both standard solutions of elemental sulphur (85 to 99% and real naphtha sample (79%. These results attest to the potential for the application of this electroanalytical methodology in determining elemental sulphur in naphtha samples containing mercaptans and disulphides.

  7. Rapid method of element determination in rye crispbread by ICP OES

    Directory of Open Access Journals (Sweden)

    Anna Szymczycha-Madeja

    2017-05-01

    Full Text Available In this work, various sample preparation procedures, i.e., microwave-assisted acid digestion in a mixture of HNO3 and H2O2 solutions, solubilisation in aqua regia or tetramethyl ammonium hydroxide and extraction in diluted HNO3 or in HCl, for the determination of the total content of Ba, Ca, Cd, Cr, Cu, Fe, Mg, Mn, Ni, P, Pb, Sr and Zn in rye crispbread using inductively coupled plasma optical emission spectrometry were compared. Analytical characteristic was evaluated by comparing the accuracy and precision of the results and limits of detection of elements. Among these five procedures solubilisation in aqua regia provides the best results, i.e., limits of detection of elements within 0.12–31.4 ng mL−1, precision of 0.4–5% and accuracy better than 5%. Additionally, a good agreement between the measured and certified values of the NIST 1567a was found for all elements. The proposed procedure is simple, reduces sample handling and minimises time and reagent consumption. Thus, it can be alternatively used instead of microwave-assisted acid digestion for routine analysis. Six different rye crispbreads were analysed with this procedure.

  8. 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

  9. Determination of the distribution coefficient of 46 elements on tin dioxide in 0.1N HNO3-acetone media

    International Nuclear Information System (INIS)

    Jaffrezic-Renault, N.

    1977-01-01

    The use of radioactive indicators for the determination of the distribution coefficients of 46 elements on SnO 2 in 0.1N HNO 3 -acetone media is described. The determination has been carried out in static conditions: labelled element solution has been agitated with SnO 2 for two hours; the elements have been labelled with radioisotopes generally obtained by (n, γ) reaction, by irradiating a part of the used salt in EL 3 or OSIRIS reactor in the C.E.N. Saclay (France). Results show that the elements may be classified into several groups, according to their oxidation state. (T.I.)

  10. Determination of rare earth elements in uranium bearing samples using Inductively Coupled Plasma Mass Spectrometry (ICPMS)

    International Nuclear Information System (INIS)

    Mishra, S.; Chaudhury, P.; Pradeepkumar, K.S.; Sahoo, S.K.

    2017-01-01

    In the present study a methodology has been described for determination of REEs without involving separation and the method is successfully applied for determination of REE concentration in uranium ore as well as in soil samples from a uranium mining site

  11. Development of radiochemical separation method for determination of toxic elements in biological samples

    International Nuclear Information System (INIS)

    Maihara, V.A.; Vasconcellos, M.B.A.; Favaro, D.I.T.; Armelin, M.J.A.

    1990-01-01

    In order to determine Hg, Sb, As and Se in biological materials by neutron activation analysis, a radiochemical separation was developed. The chemical separation procedure used was based on the digestion of the irradiated sample in a mixture of H NO 3 and H 2 SO 4 in a teflon bomb, at 130 0 C for 1 to 4 hours. After the dissolution of organic matter, Hg and Sb were retained by a Dowex 2-X8 resin column in 6 M HCl. The effluent was passed through a TDO, tin dioxide column which retains As and Se in 3 M HCl medium. Radioactive tracers of these elements were used to determine the yields of the separation process. Certified reference materials were analyzed to check the precision and accuracy of the method. (author)

  12. Development of a radiochemical separation method for toxic elements determination from biologic samples

    International Nuclear Information System (INIS)

    Malhara, V.A.; Vasconcellos, M.B.A.; Favaro, D.I.T.; Armelin, M.J.A.

    1990-01-01

    In order to determine Hg, Sb, As and Se in biological materials by neutron activation analysis, a radiochemical separation was developed. The chemical separation procedure used was based on the digestion of the irradiated sample in a mixture of HNO 3 and H 2 SO 4 in a teflon bomb, at 130 0 C for 1 to 4 hours. After the dissolution of organic matter, Hg and Sb were retained by a Dowex 2-XB resin column in 6M HCI. The efluent was passed through a TDO, tin dioxide column which retains As and Se in 3M HCI medium. Radioactive tracers of these elements were used to determine the yields of the separation process. Certified reference materials were analyzed to check the precision and accuracy of the method. (author)

  13. Finite element analysis of cylindrical indentation for determining plastic properties of materials in small volumes

    International Nuclear Information System (INIS)

    Lu, Y Charles; Kurapati, Siva N V R K; Yang Fuqian

    2008-01-01

    The cylindrical indentation is analysed, using the finite element method, for determining the plastic properties of elastic-plastic materials and the effect of strain hardening. The results are compared with those obtained from spherical indentation, the commonly used technique for measuring plastic properties of materials in small volumes. The analysis shows that the deformation under a cylindrical indenter quickly reaches a fully plastic state and that the size (diameter) of the plastic zone remains constant during further indentation. The indentation load is proportional to the indentation depth at large indentation depth, from which the indentation pressure P m at the onset of yielding can be readily extrapolated. The analysis of cylindrical indentation suggests that it does not need parameters such as impression radius (a) and contact stiffness (S) for determining the plastic behaviour of materials. Thus, the cylindrical indentation can suppress the uncertainties in measuring material properties

  14. 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.)

  15. [Simultaneous determination of multiple elements in airborne particulate samples by X-ray fluorescence spectrometry].

    Science.gov (United States)

    Takada, T; Hitosugi, M; Kadowaki, T; Kudo, M

    1983-07-01

    An energy dispersive X-ray fluorescence spectrometer (EDX) has been applied to determine multielements in the workplace air. The standards for X-ray fluorescence analysis were prepared by the chelate precipitation method on polyvinyl chloride (PVC) membrane filter. And, the specimens were prepared to deposit various metal compounds of different chemical forms by the suspension method on PVC membrane filter, and they were determined with EDX and atomic absorption spectrometer (AAS). The results obtained were as follows. Though there is a difference by each element, an amount less than 3 microgram/cm2 per unit area makes it possible to undergo multielement analysis, that is, is has no influence on fine particle effect (particle size; under 5 microns). Then, effects of the X-ray intensity by different chemical forms are negligible. At the presence the neighboring element and other elements this technique showed greater precision by carrying out on corrective treatment, etc. The coefficient of variation of this technique was in the range of 2.5-6.5% at DDTC-Cu of 0.5-5.0 micrograms/cm2, with the limit of detection for As : 0.002 microgram/cm2, Zn : 0.003 microgram/cm2, Pb : 0.003 microgram/cm2, Cu : 0.004 microgram/cm2, Ni : 0.003 microgram/cm2, Fe : 0.005 microgram/cm2, Mn : 0.008 microgram/cm2, Cr : 0.013 microgram/cm2, respectively. Aerosols collected at the workplace were analyzed with EDX and AAS, and the obtained results showed good agreement with such regression line as y = 1.04 chi + 0.04, the coefficient of correlation being r = 0.995. From these results, this technique was found to be a very excellent method for monitoring of multielements in the workplace air.

  16. Determination of the Mineral Composition and Toxic Element Contents of Propolis by Near Infrared Spectroscopy

    Directory of Open Access Journals (Sweden)

    M. Inmaculada González-Martín

    2015-11-01

    Full Text Available The potential of near infrared spectroscopy (NIR with remote reflectance fiber-optic probes for determining the mineral composition of propolis was evaluated. This technology allows direct measurements without prior sample treatment. Ninety one samples of propolis were collected in Chile (Bio-Bio region and Spain (Castilla-León and Galicia regions. The minerals measured were aluminum, calcium, iron, potassium, magnesium, phosphorus, and some potentially toxic trace elements such as zinc, chromium, nickel, copper and lead. The modified partial least squares (MPLS regression method was used to develop the NIR calibration model. The determination coefficient (R2 and root mean square error of prediction (RMSEP obtained for aluminum (0.79, 53, calcium (0.83, 94, iron (0.69, 134 potassium (0.95, 117, magnesium (0.70, 99, phosphorus (0.94, 24 zinc (0.87, 10 chromium (0.48, 0.6 nickel (0.52, 0.7 copper (0.64, 0.9 and lead (0.70, 2 in ppm. The results demonstrated that the capacity for prediction can be considered good for wide ranges of potassium, phosphorus and zinc concentrations, and acceptable for aluminum, calcium, magnesium, iron and lead. This indicated that the NIR method is comparable to chemical methods. The method is of interest in the rapid prediction of potentially toxic elements in propolis before consumption.

  17. Determination of essential elements in commercial baby foods by INAA (Instrumental Neutron Activation Analysis)

    Energy Technology Data Exchange (ETDEWEB)

    Vallinoto, Priscila; Maihara, Vera A., E-mail: pvallinoto@ipen.br, E-mail: vmaihara@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    The World Health Organization recommends that infants be breast feed exclusively at least six months after birth. After this period, it is recommended to introduce complementary foods, in order to meet nutritional amounts, minerals and energy needs of children. Commercial food products intended for infants form an important part of the diet for many babies, so it is very important that such food contains sufficient amounts of minerals. Inadequate complementary feeding is a major cause of high rates of malnutrition in developing countries. In this study, essential elements: Ca, Co, Cr, Cs, Fe, K, Na and Zn levels were determined in seven different commercial food products samples by Instrumental Neutron Activation Analysis. The seven baby food samples were acquired in the markets of Sao Paulo city. After 8-hour irradiations in the IEA-R1 nuclear research reactor under a thermal neutron flux of 10{sup 12} n cm{sup -2} s{sup -1}, the essential elements were determined and the concentrations obtained were lower than the WHO requirements. For validation of the methodology, INCT MPH-2 Mixed Polish Herbs and NIST SRM 1577{sup b} Bovine Liver were analysed. (author)

  18. Determination of essential elements in commercial baby foods by INAA (Instrumental Neutron Activation Analysis)

    International Nuclear Information System (INIS)

    Vallinoto, Priscila; Maihara, Vera A.

    2011-01-01

    The World Health Organization recommends that infants be breast feed exclusively at least six months after birth. After this period, it is recommended to introduce complementary foods, in order to meet nutritional amounts, minerals and energy needs of children. Commercial food products intended for infants form an important part of the diet for many babies, so it is very important that such food contains sufficient amounts of minerals. Inadequate complementary feeding is a major cause of high rates of malnutrition in developing countries. In this study, essential elements: Ca, Co, Cr, Cs, Fe, K, Na and Zn levels were determined in seven different commercial food products samples by Instrumental Neutron Activation Analysis. The seven baby food samples were acquired in the markets of Sao Paulo city. After 8-hour irradiations in the IEA-R1 nuclear research reactor under a thermal neutron flux of 10 12 n cm -2 s -1 , the essential elements were determined and the concentrations obtained were lower than the WHO requirements. For validation of the methodology, INCT MPH-2 Mixed Polish Herbs and NIST SRM 1577 b Bovine Liver were analysed. (author)

  19. Comparative study for essential elements determination in milk products samples by INAA and ICP-AES

    International Nuclear Information System (INIS)

    Kira, Carmen S.; Maihara, Vera A.

    2002-01-01

    The mineral elements Ca, Fe, K, Mg, Na and Zn were analyzed in milk products by using instrumental neutron activation analysis (INAA) and inductively coupled plasma atomic emission spectrometry (ICP-AES). The study included four types of cheese (mozzarella, minas, prato, parmesan), chocolate milk and yogurt. The samples were purchased from the local markets. Average concentrations ranged from 3668 (chocolate milk) to 16558 (parmesan cheese) mg/kg for Ca; from 2.61 (parmesan cheese) to 28.9 (chocolate milk) mg/kg for Fe; from 673 (mozzarella cheese) to 10492 (chocolate milk) mg/kg for K; from 398 (yogurt) to 2280 (minas cheese) mg/kg for Mg; from 1681 (yogurt) to 15248 (parmesan cheese) mg/kg for Na; from 12.1 (chocolate milk) to 71.8 (parmesan cheese) mg/kg for Zn. Two National Institute of Standards and Technology (NIST) standard reference materials (SRM 8435 Whole Milk Powder and SRM 1549 Non Fat Milk Powder) were analyzed to verify method accuracy. The statistic test used to determine the significance of the difference between the techniques was based on Unpaired t-Student test. Statistical test revealed no significance differences (P< 0,05) between the average values provided by the two methods for the most of determined elements. (author)

  20. Application of AmBe source neutron irradiator for determination of inorganic elements in commercial fertilizers

    International Nuclear Information System (INIS)

    Madi Filho, Tufic; Armelim, Maria Jose Aguirre; Fulas, Paulo Marcelo Marangon; Trevizam, Anderson Ricardo; Figueira, Rubens Cesar Lopes

    2005-01-01

    The rational use of fertilizers , for the soil fertility correction, contributes to the increase of agricultural production, using the same areas previously available. The quality of products could ne improved with reduced costs. Therefore, knowledge of the chemical characteristics of the correctives used is required to streamline the application and avoid excesses or deficiencies. The studied characteristics are generally limited to the essential nutrients for the nutrition of plants and animals, e.g.: Mn, Zn, P, K, Cu and those known toxic, such as: As, Cd, Hg and Pb. Neutron activation analysis (NAA) is a highly sensitive non destructive technique, for the determination of the elemental composition in samples. It has been particularly useful in the simultaneous determination of inorganic elements in complex samples of several kinds. Several analysis methods for activation are used, such as: comparative and absolute. Commercial fertilizers were analyzed applying the absolute and comparative methods. Using the absolute method, samples were submitted to neutron flux generated by an irradiator with two Am Be sources. The obtained results were compared with those obtained by the comparative method using neutrons generated in the IEA-R1 Reactor. (author)

  1. Determination of Heavy Metals and Radioactive Elements in Alluvial Soil using Atomic Absorption and Gamma Spectroscopy

    International Nuclear Information System (INIS)

    Hamed, S.S.; Walley EI Dine, N.; Soliman, S.I.; Moussa, W.M.

    2008-01-01

    The paper describes some methods dealing with measurements of some heavy and radioactive elements (U, Th and K) in Egyptian cultivated soil samples. Samples were collected from Toshka area. Also, soil and plant samples were collected from Kalube and EI - Gabal EI - Asfar to compare the obtained results from both region. Flame atomic absorption spectrometry (FAAS),Neutron activation analysis (INAA) and Natural radioactivity techniques were followed. FAAS and INAA techniques agreed fairly well for the compared elements Co,Zn and Fe which determined by the two techniques. Also for K which was determined by FAAS and natural radioactivity. It was found that the concentration range in soil samples for Co, Fe, K and Zn lies between 4.18 and 29.2 μg/g, 3.0 and 3.8 mg/g, 3.49 and 13.28 mg/g and 120 and 663 μg/g respectively while in plant samples the concentration of Co was from 3.02 to 4.02 μg/g, Fe from 1.18 to 1.35 mg/g and Zn from 29.63 to 73.02 μg/g

  2. 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)

  3. 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

  4. [Determination of Heavy Metal Elements in Diatomite Filter Aid by Inductively Coupled Plasma Mass Spectrometry].

    Science.gov (United States)

    Nie, Xi-du; Fu, Liang

    2015-11-01

    This study established a method for determining Be, Cr, Ni, As, Cd, Sb, Sn, Tl, Hg and Pb, total 10 heavy metals in diatomite filter aid. The diatomite filter aid was digested by using the mixture acid of HNO₃ + HF+ H₃PO₄ in microwave system, 10 heavy metals elements were determined by inductively coupled plasma mass spectrometry (ICP-MS). The interferences of mass spectrometry caused by the high silicon substrate were optimized, first the equipment parameters and isotopes of test metals were selected to eliminate these interferences, the methane was selected as reactant gas, and the mass spectral interferences were eliminated by dynamic reaction cell (DRC). Li, Sc, Y, In and Bi were selected as the internal standard elements to correct the interferences caused by matrix and the drift of sensitivity. The results show that the detection limits for analyte is in the range of 3.29-15.68 ng · L⁻¹, relative standard deviations (RSD) is less than 4.62%, and the recovery is in the range of 90.71%-107.22%. The current method has some advantages such as, high sensitivity, accurate, and precision, which can be used in diatomite filter aid quality control and safety estimations.

  5. Homology of polytene elements between Drosophila and Zaprionus determined by in situ hybridization in Zaprionus indianus.

    Science.gov (United States)

    Campos, S R C; Rieger, T T; Santos, J F

    2007-05-09

    The drosophilid Zaprionus indianus due to its economical importance as an insect pest in Brazil deserves more investigation into its genetics. Its mitotic karyotype and a line-drawing map of its polytene chromosomes are already available. This paper presents a photomap of Z. indianus polytene chromosomes, which was used as the reference map for identification of sections marked by in situ hybridization with gene probes. Hybridization signals for Hsp70 and Hsr-omega were detected, respectively, in sections 34B and 32C of chromosome V of Z. indianus, which indicates its homology to the chromosomal arm 3R of Drosophila melanogaster and, therefore, to Muller's element E. The main signal for Hsp83 gene probe hybridization was in section 17C of Z. indianus chromosome III, suggesting its homology to arm 3L of D. melanogaster and to element D of Muller. The Ubi probe hybridized in sections 10C of chromosome II and 17A of chromosome III. Probably the 17A is the polyubiquitin locus, with homology to arm 3L of D. melanogaster and to the mullerian D element, as suggested also by Hsp83 gene location. The Br-C gene was mapped in section 1D, near the tip of the X chromosome, indicating its homology to the X chromosome of D. melanogaster and to mullerian element A. The Dpp gene probe hybridized mainly in the section 32A of chromosome V and, at lower frequencies to other sections, although no signal was observed as expected in the correspondent mullerian B element. This result led to the suggestion of a rearrangement including the Dpp locus in Z. indianus, the secondary signals possibly pointing to related genes of the TGF-beta family. In conclusion, the results indicate that chromosomes X, III, V of Z. indianus are respectively correspondents to elements A, D, and E of Muller. At least chromosome V of Z. indianus seems to share synteny with the 3R arm of D. melanogaster, as indicated by the relative positions of Hsp70 and Hsr-omega, although the Dpp gene indicates a disruption of

  6. Isotope Methods in Determining The Water Budget Elements; Su Buetcesi Elemanlarinin Bulunmasinda Izotop Yoentemi

    Energy Technology Data Exchange (ETDEWEB)

    Oezaydin, V [DSI, Technical Research and Quality Control Department, Ankara (Turkey)

    2002-07-01

    One of the main aims of the water engineers is the determination of the inflows to and outflows from a natural or artificial lake. According to the classical water balance equation inflows (precipitation on the lake surface, surface and subsurface inflows) mines the outflows (evaporation from lake surface, surface and subsurface outflows) should be equal to the volume change in a specified time interval. With the classical water budget equation it is possible to determine the total absolute subsurface inflow mines outflow but it is not possible to determine them separately. The two unknowns could be determined with one more equation. The isotopes, oxygen-18, deuterium or tritium, which are naturally present in water, could provide the extra equation by writing the isotopic mass balance equation. In this study, the theoretical background of isotope technique and application to Mogan Lake, will be presented which is used in determining the water budget of lakes.

  7. Multielement determination of major-to-ultratrace elements in vegetable samples by ICP-MS and ICP-AES after acid digestion

    International Nuclear Information System (INIS)

    Hokura, Akiko; Oguri, Sachiko; Matsuura, Hirotaka; Haraguchi, Hiroki

    2000-01-01

    A multielement determination of major-to-ultratrace elements in vegetable samples was carried out by inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma atomic emission spectrometry (ICP-AES). Spinach samples (0.5 g) were digested with nitric acid and hydrofluoric acid in a Teflon beaker on a hot plate. The decomposed samples were dissolved in a 1 M ( = mol dm -3 ) HNO 3 solution containing internal standard elements (Ge, In, and Re, 10 ppb each), and were subjected to multielement analyses by ICP-AES and ICP-MS. As a result, about 40 elements were successfully determined over a wide concentration range from % to ppb level. Spinach samples grown in different production areas were also analyzed in order to understand the influences of the environmental conditions on growth. Among the major and minor elements, the values of the coefficient of variance (CV) for B, Mg, P, and K were < 20%, and those for Ca, Na, Al, and Mn were higher than 50%. On the other hand, the values of CV for trace and ultratrace elements were significantly high. Furthermore, the present analytical method was also applied to the determination of major-to-ultratrace elements in various vegetable samples (23 species in 11 families); the similarities and differences of the elemental distributions in vegetables were found in the experimental results. (author)

  8. Multielement determination of major-to-ultratrace elements in vegetable samples by ICP-MS and ICP-AES after acid digestion

    Energy Technology Data Exchange (ETDEWEB)

    Hokura, Akiko; Oguri, Sachiko; Matsuura, Hirotaka; Haraguchi, Hiroki [Dept. of Applied Chemistry, Graduate School of Engineering, Nagoya Univ. (Japan)

    2000-06-01

    A multielement determination of major-to-ultratrace elements in vegetable samples was carried out by inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma atomic emission spectrometry (ICP-AES). Spinach samples (0.5 g) were digested with nitric acid and hydrofluoric acid in a Teflon beaker on a hot plate. The decomposed samples were dissolved in a 1 M ( = mol dm{sup -3}) HNO{sub 3} solution containing internal standard elements (Ge, In, and Re, 10 ppb each), and were subjected to multielement analyses by ICP-AES and ICP-MS. As a result, about 40 elements were successfully determined over a wide concentration range from % to ppb level. Spinach samples grown in different production areas were also analyzed in order to understand the influences of the environmental conditions on growth. Among the major and minor elements, the values of the coefficient of variance (CV) for B, Mg, P, and K were < 20%, and those for Ca, Na, Al, and Mn were higher than 50%. On the other hand, the values of CV for trace and ultratrace elements were significantly high. Furthermore, the present analytical method was also applied to the determination of major-to-ultratrace elements in various vegetable samples (23 species in 11 families); the similarities and differences of the elemental distributions in vegetables were found in the experimental results. (author)

  9. 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)

  10. Detection, in real time, of metallic pollutants present in the industrial atmospheric effluents by inductively coupled plasma torch; Detection, en temps reel, d'elements metalliques presents dans les rejets atmospheriques industriels par torche a plasma a couplage inductif

    Energy Technology Data Exchange (ETDEWEB)

    Vacher, D.

    2001-12-15

    This work is devoted to the development of a process of detection in real time of metallic pollutants present in industrial atmospheric effluents. The method of measurement is the atomic spectrometry of emission coupled to an ICP torch (Inductively coupled Plasma). The technology of the fluidized beds is used as system of introduction of the metallic particles into the ICP torch, the interest of the principle of detection resting on the stamping from the usual procedure of calibration of the analytical system. The results are presented in two parts. The first relates to the diagnosis of plasmas formed with various mixtures of N{sub 2}/O{sub 2} which one corresponds to pure air, the second presents the setting process of detection in real time starting from the intensities ratios of the spectral lines of the metallic element with those of the plasma-producing element (argon or pure air) The study of the diagnosis of plasmas made up of mixtures N{sub 2}/O{sub 2} relates to the determination of the atomic excitation temperature from the spectral lines of the copper element and the evaluation of the thermal disequilibrium q Te/Th. This last is obtained by considering the mass enthalpy of various mixtures N{sub 2}/O{sub 2}. The existence of a small thermal disequilibrium is highlighted. The study of detection in real time by ICP torch, without calibration of the system, is based on three points: - spectroscopic data processing to determine the values of the intensities ratios of spectral lines; - the insertion of the intensities ratios and the characteristics of plasma (argon or pure air) into a calculation code of plasma composition; - the comparison of the mass flux values of the metallic pollutants, in real time, obtained by experiments with those resulting from the elutriation calculation, term which defines the phenomenon of entrainment of the particles out of the fluidized bed. The results made it possible to show the similarity of the analytical system response

  11. Determination of multi-element profiles of soil at Visakhapatnam using EDXRF technique

    International Nuclear Information System (INIS)

    Sandeep, P.; Kothai, P.; Dusane, C.B.; Sahu, S.K.; Pandit, G.G.

    2014-01-01

    In the present study attempt has been made to generate elemental profile database for major sources of soil pollution, specific to Visakhapatnam. Representative road dust and soil samples from major industrial locations were collected and analyzed for various metals distribution using EDXRF. Analysis results indicate that V and Ni were predominant at PR and Zn was found to be dominating in road dust samples. Higher concentration of Arsenic was observed at TPP as compared to all other sites. Cr was found to be dominating at TPP and SP. I geo calculations suggest that soil is highly contaminated with heavy metal pollutants. (author)

  12. 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.

  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. FLOW INJECTION ANALYSIS SYSTEM COUPLED WITH ICP-EOS FOR DETERMINATION OF SOME METALLIC ELEMENTS IN DRINKING WATER

    Directory of Open Access Journals (Sweden)

    Cristina Dinu

    2009-06-01

    Full Text Available The European Drinking Water Directive (98/83/EC, transposed in Romanian Legislation as Low 458/2002, amended by Low 311/2004, imposes the limit of concentration for metallic elements in water intended for human consumption. The toxic metals arsenic and selenium are among these elements and the limit value is 10 μg/L. In the paper there are presented the working conditions for determination of As and Se from drinking water using modern techniques based on the fl ow injection-hydride generation with the inductively coupled plasma atomic emission spectrometry (FIAS-ICP-EOS. The analyses were performed on Optima 5300 DV Perkin Elmer equipment with FIAS 400 Flow Injection System, Perkin Elmer type. For the hydride generation two types of solution were used: 10% (v/v HCl as a carrier solution and 0.2 % NaBH4 in 0.05%NaOH solution as a reducing agent [1]. The treatment step of the samples and standard solutions consisted in reducing with mixed solutions of KI and ascorbic acid in acidic condition (HCl for As and only with HCl and high temperature for Se [2,3]. The paper contains the characteristic parameters of the methods, such as: low detection limit, quantifi cation limit, repeatability, precision, recovery, which were evaluated using Certifi ed Reference Materials for each element.

  15. Radioactivation and X-ray fluorescence methods of determination of some elements in atmospheric air and waters

    International Nuclear Information System (INIS)

    Kulmatov, R.A.; Kist, A.A.; Karimov, I.I.; Pulatov, D.D.; Kamil'dzhanov, A.Kh.

    1981-01-01

    Possibilities of instrumental radioactivation and X-ray fluorescence method of determining certain elements in aerosols and waters in the region of metallurgic production location and around it are considered. For conducting instrumental radioactivation analysis the samples have been irradiated on filter during 20h in the thermal neutron flux f=10 13 neutr/cm 2 xs of nuclear reactor-WWR-SM INP ASUzSSR. Measurement of induced activity has been conducted after 7 and 15-day cooling by means of Ge(Li) detectors. Averaged results of instrumental radioactivation and X-ray fluorescence analysis of element (Cu, Zn, Fe, Pb) composifion of some samples are presented. Content of such elements as copper, zinc, lead in the industrial region several times exceeds usual background content that is caused by industrial releases. Toxic effect, rate of aerosol release from atmosphere and radius of harmful effect of industrial enterprises on environment much depends on dispersion. A set of filter materials differing from one another by pore diameter have been used for conducting dispersion analysis of aerosals [ru

  16. The determination of minor amounts of rare earth elements in high purity earth oxides by HPLC/IDMS

    International Nuclear Information System (INIS)

    Stijfhoorn, D.E.; Stray, H.; Hjelmseth, H.

    1991-05-01

    Since the early seventies isotopic dilution mass spectrometry (IDMS) has been used at Institutt for energiteknikk, Kjeller, Norway for determination and certification of rare earth elements in high purity Y 2 O 3 . These lanthanides have, during the last few decades, become more widely used in highly specialized technology. High purity, quality 4 N (99.99%) or even 5 N materials are needed for phosphors, lasers, optical fibers, X-ray films, and in contrast fluids for magnetic resonance imaging (MRI). However, in a matrix constisting primarily of a single lanthanide, IDMS alone will not be effective due to isobaric interferences from the main elements or the mono-oxides formed in the ion source. On the other hand, high performance liquid chromatography (HPLC) may be used, but the detection limit will be in the order of 5 to 10 ppm/W. In this work a combination of HPLC and IDMS has been used to lower the detection limit to 1 ppm/W, where the sample is spiked before separation by HPLC, followed by IDMS analysis of the HPLC- fractions. In some cases the HPLC-process has to be repeated to remove the main element completly. Results are presented for Dy 2 O 3 and Nd 2 O 3 , but similar separating procedures can be applied for other rare earth oxides. 3 refs., 2 figs. 2 tabs

  17. Element determination in natural biofilms of mine drainage water by total reflection X-ray fluorescence spectrometry

    International Nuclear Information System (INIS)

    Mages, Margarete; Tuempling, Wolf von Jr.; Veen, Andrea van der; Baborowski, Martina

    2006-01-01

    Human impacts like mining activities lead to higher element concentration in surface waters. For different pollution levels, the consequences for aquatic organisms are not yet investigated in detail. Therefore, the aim of this investigation is to determine the influence of mining affected surface waters on biofilms. Elements like heavy metals can be absorbed on cell walls and on polymeric substances or enter the cytoplasm of the cells. Thus, they are important for the optimization of industrial biotechnological processes and the environmental biotechnology. Beyond this, biofilms can also play an important role in wastewater treatment processes and serve as bioindicators in the aquatic environment. The presented total reflection X-ray fluorescence spectroscopic investigation was performed to compare the element accumulation behavior of biofilms grown on natural or on artificial materials of drainage water affected by former copper mining activities. A high salt and heavy metal pollution is characteristic for the drainage water. For an assessment of these results, samples from stream Schlenze upstream the confluence with the drainage water, a small tributary of the Saale River in central Germany, were analyzed, too

  18. 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)

  19. 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)

  20. The Determination of Composite Elements in Zircaloy-2 by X-Ray Fluorescence and Emission Spectrometry Method

    International Nuclear Information System (INIS)

    Dian Anggraini; Rosika Kriswarini; Yusuf N

    2007-01-01

    Analysis of composing elements in zircaloy-2 has been done by Emission Spectrometry method and X-Ray Fluorescence (XRF). The aim of the analysis is to verify conformity between composing elements in zircaloy-2 and the material certificate. Spectrometry Emission method has higher sensitivity in element determination of a material than that of XRF method, so can be estimated that emission spectrometry method has higher accuracy than that of XRF method. The result of qualitative analysis by Emission Spectrometry indicate that the composing elements in zircaloy-2 were Sn, Cr and Ni. However, the qualitative analysis result by XRF method indicated that the composing elements in zircaloy 2 were Sn, Cr, Ni and Fe. Fe element can not be analysed by Emission Spectrometry method because Emission Spectrometer did not equipped with Fe detector. The quantitative analysis result of the composing elements in the material with both methods showed that Sn, Cr and Ni concentration of zircaloy 2 existed in concentration ranges of the material certificate. Result of statistical test (F and t-test) of analysis result of both methods can be used for analyzing composing elements in zircaloy 2. Emission Spectrometry method was more sensitive and accurate for determining Cr and Ni element in zircaloy 2 than that of emission Spectrometry method but both methods had same accuracy. The precision of measurement of Sn, Cr and Ni element using XRF method was better than that of Emission spectrometry method. (author)

  1. 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.

  2. 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)

  3. Application of neutron activation analysis technique in elemental determination of lichen samples

    International Nuclear Information System (INIS)

    Djoko Prakoso Dwi Atmodjo; Syukria Kurniawati; Woro Yatu Niken Syahfitri; Nana Suherman; Dadang Supriatna

    2010-01-01

    Lichen is one of the biological materials as pollution monitor that can give information about level, direction, and history of various pollutants in environment. Small sample weights and elemental content of lichens is on the order of ppm, so that its characterization requires advanced analytical techniques that has high sensitivity and capable of analyzing samples with weight of - 25 mg, such as neutron activation analysis. In this research, determination of elements was done in lichen samples obtained from Kiaracondong and Holis areas in Bandung city, to understanding the difference of industrial exposure level on surrounding environment. Samples were irradiated in RSG GA Siwabessy, Serpong, at 15 MW for 1-2 and 60 minutes for short irradiation and long irradiation, respectively. The samples were then counted using HPGe detector with GENIE 2000 software. The level of element in lichen for Kiaracondong area were Co, Cr, Cs, Fe, Mg, Mn, Sb, Sc, and V in the range of 0.55-0.86, 1.47-2.57, 0.87-1.19, 540-1005, 949-1674, 34.91-45.94, 0.08-0.14, 0.16-0.31, and ≤ 2.33 mg/kg, respectively, while for Holis area were 1.04-2.37, 4.41-10.36, 0.41-0.89, 3166-709, 1131-1422, 40.97-72.51, 0.33-0.50, 0.98-2.18, and 5.30-13.05 mg/kg respectively. From these results, it is known that pollution exposure from the semi industrial area Holis provide greater influence than in the semi industrial area Kiaracondong. (author)

  4. 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)

  5. The fuel element of the first charge for EL 4; presentation, main problems arising in the research, production problems; L'element combustible du 1. jeu de EL 4; presentation, problemes essentiels poses par l'etude, problemes de fabrication

    Energy Technology Data Exchange (ETDEWEB)

    Ringot, C; Bailly, H; Bujas, R [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    The fuel element making up the first charge for EL-4 is made of slightly enriched uranium oxide canned in stainless steel. This fuel element makes it possible to operate the reactor in the safest conditions awaiting the development of the fuel which will be finally adopted; this will have a low absorption can: beryllium, or a zirconium copper alloy. The 500 mm assembly is made up of 19 small rods placed on 3 rings, inside a graphite jacket. The solution adopted was a solution using completely independent small rods. This report deals with possible problems resulting from their study and production. (authors) [French] L'element combustible du 1er jeu EL-4 est un element combustible a oxyde d'uranium legerement enrichi gaine d'acier inoxydable. C'est un element combustible permettant de faire fonctionner le reacteur EL 4 dans des conditions aussi sures que possible avant de mettre au point le combustible definitif qui sera a gaine peu absorbante: beryllium, ou alliage zirconium-cuivre. L'assemblage de longueur 500 mm est constitue de 19 crayons places sur 3 couronnes, a l'interieur d'une chemise de graphite. La solution adoptee a ete une solution a crayons independants les uns des autres. Ce rapport traite des problemes eventuels poses par leur etude et leur fabrication. (auteurs)

  6. Correlating laser-induced breakdown spectroscopy with neutron activation analysis to determine the elemental concentration in the ionome of the Populus trichocarpa leaf

    Science.gov (United States)

    Martin, Madhavi Z.; Glasgow, David C.; Tschaplinski, Timothy J.; Tuskan, Gerald A.; Gunter, Lee E.; Engle, Nancy L.; Wymore, Ann M.; Weston, David J.

    2017-12-01

    The black cottonwood poplar (Populus trichocarpa) leaf ionome (inorganic trace elements and mineral nutrients) is an important aspect for determining the physiological and developmental processes contributing to biomass production. A number of techniques are used to measure the ionome, yet characterizing the leaf spatial heterogeneity remains a challenge, especially in solid samples. Laser-induced breakdown spectroscopy (LIBS) has been used to determine the elemental composition of leaves and is able to raster across solid matrixes at 10 μm resolution. Here, we evaluate the use of LIBS for solid sample leaf elemental characterization in relation to neutron activation. In fact, neutron activation analysis is a laboratory-based technique which is used by the National Institute of Standards and Technology (NIST) to certify trace elements in candidate reference materials including plant leaf matrices. Introduction to the techniques used in this research has been presented in this manuscript. Neutron activation analysis (NAA) data has been correlated to the LIBS spectra to achieve quantification of the elements or ions present within poplar leaves. The regression coefficients of calibration and validation using multivariate analysis (MVA) methodology for six out of seven elements have been determined and vary between 0.810 and 0.998. LIBS and NAA data has been presented for the elements such as, calcium, magnesium, manganese, aluminum, copper, and potassium. Chlorine was also detected but it did not show good correlation between the LIBS and NAA techniques. This research shows that LIBS can be used as a fast, high-spatial resolution technique to quantify elements as part of large-scale field phenotyping projects.

  7. A NOR-associated repetitive element present in the genome of two Salmo species (Salmo salar and S. trutta)

    Digital Repository Service at National Institute of Oceanography (India)

    Abuin, M.; Clabby, C.; Martinez, P.; Goswami, U.; Flavin, F.; Wilkins, N.P.; Houghton, J.A.; Powell, R.; Sanchez, L.

    , internal repetition, and long direct repeats with deletions and insertions between individual units. The repetitive element was shown to have a tandem unit arrangement and was estimated to occupy between two and three percent of the Atlantic salmon genome...

  8. Determination of rare earth elements by photometric microtitration using xylenol orange

    International Nuclear Information System (INIS)

    Kuban, V.; Jancarova, I.; Sommer, L.

    1989-01-01

    Stock solutions were prepared of rare earth elements in approx 0.1M nitric acid, xylenol orange and EDTA. All measurements were made using a double-beam digital recording spectrophotometer (Superscan 3) with a titration measuring cell with a volume of approx. 30 ml and optical length of 20 mm. Titration agents were pipetted using an automatic piston microburette. Measured were absorbance pH curves of solutions of several lanthanides with xylenol orange, the absorption spectra of solutions of xylenol orange with lanthanides with increasing addition of titration agents EDTA, and the titration curves of the dependence of absorbance of lanthanide solutions with xylenol orange during titration with the EDTA solution. It was found that photometric microtitration allowed accurate and correct determination of all rare earth elements within the concentration range 0.04 - 0.5 mmol/l by titration with standard EDTA solution of a concentration of xylenol orange of 20 μmol/l. (E.S.). 4 figs., 3 tabs., 7 refs

  9. INAA in the determination of the elemental constituents of a natural fluorite

    International Nuclear Information System (INIS)

    Balogun, F.A.; Tubosun, I.A.; Adesanmi, C.A.; Ajao, J.A.; Akanle, A.O.; Spyrou, N.M.; Ojo, J.O.

    1997-01-01

    A complementary use of the comparative and the semi-absolute variations of instrumental neutron activation analysis (INAA) has enabled us to determine 22 different elements in a sample of natural fluorite originating from the younger granite province of Nigeria. The mineral has a brownish purple appearance with some veinlets having a deep purple coloration. Of all the 22 elements measured, Fe (851.36 ppm), Sb (7.69 ppm), Ag (87.4 ppm), Hg (2.71 ppm) and Se (1.97 ppm) are found to be exclusive to the veinlets while Au (109.15 ppm), Co (2.15 ppm) and W (173.20 ppm) are concentrated in the main matrix of the fluorite. With the aid of the semi-absolute method, it was possible to measure the Au concentration in the IAEA Soil-7 reference material to be 56.83±5.87% ppm. A qualitative electron microprobe analysis (EMA) showed that the bulk of the matrix is composed mainly of Ca and F, as expected. (author)

  10. Determination of essential elements in food and feed materials by atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Yawar, W.; Rahman, S.

    1993-01-01

    Determination of baseline levels of essential elements like iron, copper, manganese and zinc was carried out in different varieties of animal feeds and in wheat grains by atomic absorption spectrophotometry. Various food articles contain different amount of essential elements. The precision and accuracy have been calculated. The range of values of iron, copper, manganese and zinc in animal feeds in form 389+-12 to 7465+-222 micro g/g; 1.1 to 3.1 +- 0.5 micro g/g; 27 +- to 267 micro g/g and 46 +- 5 to 245 + 12 micro g/g, respectively whereas the range in wheat grains for iron, copper, manganese and zinc is 40 +- 2 to 55 +- micro g/g; 6 +- 0.5 to 16 +- 2 micro g/g; 35 +- 3 to 67 +- 4.3 micro g/g and 38 +- 2.7 to 64 +- 3.34 micro g/g, respectively. In order to check the accuracy, NBs reference materials, SRM-1567 (wheat flour) and SRM-1571 (orchard leaves) were analysed. The values so obtained were found to be in fairly good agreement with the standard values. The results were also compared with other reported values. (author)

  11. Determination of rare earth elements in seawater by inductively coupled plasma-mass spectrometry

    International Nuclear Information System (INIS)

    Moeller, P.; Dulski, P.; Luck, J.

    1992-01-01

    Shortly after sampling, rare earth elements (REEs) from 11.5 l of seawater were concentrated in 35 ml solutions by ion exchange chromatography on board the German research vessel ''Sonne'' using Chelex 100 chelating resin for preconcentration. Two millilitres of a 0.2 μg g -1 Lu spike was added to the seawater samples (i) for monitoring the chemical yield which was always found to vary between 85 and 112% (mean: 100±6) and (ii) as an internal standard. Rare earth elements have been determined by ICP-MS, with REE concentrations ranging from 100 (La) to 1 (Eu) pmol kg -1 . La in blanks can be as high as 30 pmol kg -1 , but blank concentrations for other REEs range between 0.5 and 0.01 pmol kg -1 . The trend of the precision of relative response factors varies between 12% (La) and 4% (Yb). The accuracy is estimated to be about 10% with the exception of La and Ce. Methodology improvements are suggested. (author)

  12. Determination of rare-earth elements content in granitic rocks by argon plasma emission spectrometry

    International Nuclear Information System (INIS)

    Merodio, J.C.; Martinez, J.M.

    1990-01-01

    A method has been developed that enables the rare-earth elements in granitic rocks to be measured sequentially, using an inductively coupled plasma (ICP) source spectrometer with medium spectral resolution (0,02nm). The rocks were dissolved in an open system with a mixture of nitric-hydrofluoric-perchloric acids. Any residues remaining at this stage were removed by filtration and digested using a mini-fusion method with lithium tetraborate. Prior to the excitation in the spectrometer the rare-earth group was separated from other constituents using cation-exchange chromatography. A detailed study of spectral interferences and the evaluation of the detection limits have been performed. Five geochemical reference sample (granitic rocks) were analyzed and the obtained results agree favourably with recommended values and with reported determinations, using high spectral resolution ICP spectrometry. (Author) [es

  13. 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

  14. Finite Element Analysis of Simple Rectangular Microstrip Sensor for Determination Moisture Content of Hevea Rubber Latex

    Science.gov (United States)

    Yahaya, NZ; Ramli, MR; Razak, NNANA; Abbas, Z.

    2018-04-01

    The Finite Element Method, FEM has been successfully used to model a simple rectangular microstrip sensor to determine the moisture content of Hevea rubber latex. The FEM simulation of sensor and samples was implemented by using COMSOL Multiphysics software. The simulation includes the calculation of magnitude and phase of reflection coefficient and was compared to analytical method. The results show a good agreement in finding the magnitude and phase of reflection coefficient when compared with analytical results. Field distributions of both the unloaded sensor as well as the sensor loaded with different percentages of moisture content were visualized using FEM in conjunction with COMSOL software. The higher the amount of moisture content in the sample the more the electric loops were observed.

  15. Multielement determination of rare earth elements in rock sample by liquid chromatography / inductively coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    Hamanaka, Tadashi; Itoh, Akihide; Itoh, Shinya; Sawatari, Hideyuki; Haraguchi, Hiroki.

    1995-01-01

    Rare earth elements in geological standard rock sample JG-1 (granodiolite)issued from the Geological Survey of Japan have been determined by a combined system of liquid chromatography and inductively coupled plasma mass spectrometry. (author)

  16. 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.

  17. 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

  18. 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

  19. 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

  20. 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.)