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Sample records for sample neutron activation

  1. Neutron activation analysis of geochemical samples

    International Nuclear Information System (INIS)

    Rosenberg, R.; Zilliacus, R.; Kaistila, M.

    1983-06-01

    The present paper will describe the work done at the Technical Research Centre of Finland in developing methods for the large-scale activation analysis of samples for the geochemical prospecting of metals. The geochemical prospecting for uranium started in Finland in 1974 and consequently a manually operated device for the delayed neutron activation analysis of uranium was taken into use. During 1974 9000 samples were analyzed. The small capacity of the analyzer made it necessary to develop a completely automated analyzer which was taken into use in August 1975. Since then 20000-30000 samples have been analyzed annually the annual capacity being about 60000 samples when running seven hours per day. Multielemental instrumental neutron activation analysis is used for the analysis of more than 40 elements. Using instrumental epithermal neutron activation analysis 25-27 elements can be analyzed using one irradiation and 20 min measurement. During 1982 12000 samples were analyzed for mining companies and Geological Survey of Finland. The capacity is 600 samples per week. Besides these two analytical methods the analysis of lanthanoids is an important part of the work. 11 lanthanoids have been analyzed using instrumental neutron activation analysis. Radiochemical separation methods have been developed for several elements to improve the sensitivity of the analysis

  2. Large Sample Neutron Activation Analysis of Heterogeneous Samples

    International Nuclear Information System (INIS)

    Stamatelatos, I.E.; Vasilopoulou, T.; Tzika, F.

    2018-01-01

    A Large Sample Neutron Activation Analysis (LSNAA) technique was developed for non-destructive analysis of heterogeneous bulk samples. The technique incorporated collimated scanning and combining experimental measurements and Monte Carlo simulations for the identification of inhomogeneities in large volume samples and the correction of their effect on the interpretation of gamma-spectrometry data. Corrections were applied for the effect of neutron self-shielding, gamma-ray attenuation, geometrical factor and heterogeneous activity distribution within the sample. A benchmark experiment was performed to investigate the effect of heterogeneity on the accuracy of LSNAA. Moreover, a ceramic vase was analyzed as a whole demonstrating the feasibility of the technique. The LSNAA results were compared against results obtained by INAA and a satisfactory agreement between the two methods was observed. This study showed that LSNAA is a technique capable to perform accurate non-destructive, multi-elemental compositional analysis of heterogeneous objects. It also revealed the great potential of the technique for the analysis of precious objects and artefacts that need to be preserved intact and cannot be damaged for sampling purposes. (author)

  3. Large sample neutron activation analysis of a reference inhomogeneous sample

    International Nuclear Information System (INIS)

    Vasilopoulou, T.; Athens National Technical University, Athens; Tzika, F.; Stamatelatos, I.E.; Koster-Ammerlaan, M.J.J.

    2011-01-01

    A benchmark experiment was performed for Neutron Activation Analysis (NAA) of a large inhomogeneous sample. The reference sample was developed in-house and consisted of SiO 2 matrix and an Al-Zn alloy 'inhomogeneity' body. Monte Carlo simulations were employed to derive appropriate correction factors for neutron self-shielding during irradiation as well as self-attenuation of gamma rays and sample geometry during counting. The large sample neutron activation analysis (LSNAA) results were compared against reference values and the trueness of the technique was evaluated. An agreement within ±10% was observed between LSNAA and reference elemental mass values, for all matrix and inhomogeneity elements except Samarium, provided that the inhomogeneity body was fully simulated. However, in cases that the inhomogeneity was treated as not known, the results showed a reasonable agreement for most matrix elements, while large discrepancies were observed for the inhomogeneity elements. This study provided a quantification of the uncertainties associated with inhomogeneity in large sample analysis and contributed to the identification of the needs for future development of LSNAA facilities for analysis of inhomogeneous samples. (author)

  4. Neutron activation analysis for antimetabolites. [in food samples

    Science.gov (United States)

    1973-01-01

    Determination of metal ion contaminants in food samples is studied. A weighed quantity of each sample was digested in a concentrated mixture of nitric, hydrochloric and perchloric acids to affect complete solution of the food products. The samples were diluted with water and the pH adjusted according to the specific analysis performed. The samples were analyzed by neutron activation analysis, polarography, and atomic absorption spectrophotometry. The solid food samples were also analyzed by neutron activation analysis for increased sensitivity and lower levels of detectability. The results are presented in tabular form.

  5. Thermal neutron self-shielding correction factors for large sample instrumental neutron activation analysis using the MCNP code

    International Nuclear Information System (INIS)

    Tzika, F.; Stamatelatos, I.E.

    2004-01-01

    Thermal neutron self-shielding within large samples was studied using the Monte Carlo neutron transport code MCNP. The code enabled a three-dimensional modeling of the actual source and geometry configuration including reactor core, graphite pile and sample. Neutron flux self-shielding correction factors derived for a set of materials of interest for large sample neutron activation analysis are presented and evaluated. Simulations were experimentally verified by measurements performed using activation foils. The results of this study can be applied in order to determine neutron self-shielding factors of unknown samples from the thermal neutron fluxes measured at the surface of the sample

  6. Neutron activation analysis for environmental sample in Thailand

    International Nuclear Information System (INIS)

    Busamongkol, Arporn; Nouchpramool, Sunun; Bunprapob, Supamatthree; Sumitra, Tatchai

    2003-01-01

    Neutron Activation Analysis has been applied for the trace elements analysis in environmental samples. Thirty three samples of airborne particulate were collected every week at Ongkharak Nuclear Research Center (ONRC) during the period of June 1998 to March 1999. The Ti, I, Mg, Na, V, K, Cl, Al, Mn, Ca, As, Sm, Sb, Br, La, Ce, Th, Cr, Cs, Sc, Rb, Fe, Zn and Co were analyzed by Neutron Activation Analysis utilizing 2 MW TRIGA MARK III research reactor. The certified reference materials 1632a and 1633a from National Bureau of Standard were select as standard. (author)

  7. Accounting for the thermal neutron flux depression in voluminous samples for instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Overwater, R.M.W.; Hoogenboom, J.E.

    1994-01-01

    At the Delft University of Technology Interfaculty Reactor Institute, a facility has been installed to irradiate cylindrical samples with diameters up to 15 cm and weights up to 50 kg for instrumental neutron activation analysis (INAA) purposes. To be able to do quantitative INAA on voluminous samples, it is necessary to correct for gamma-ray absorption, gamma-ray scattering, neutron absorption, and neutron scattering in the sample. The neutron absorption and the neutron scattering are discussed. An analytical solution is obtained for the diffusion equation in the geometry of the irradiation facility. For samples with known composition, the neutron flux--as a function of position in the sample--can be calculated directly. Those of unknown composition require additional flux measurements on which least-squares fitting must be done to obtain both the thermal neutron diffusion coefficient D s and the diffusion length L s of the sample. Experiments are performed to test the theory

  8. Determination of average activating thermal neutron flux in bulk samples

    International Nuclear Information System (INIS)

    Doczi, R.; Csikai, J.; Doczi, R.; Csikai, J.; Hassan, F. M.; Ali, M.A.

    2004-01-01

    A previous method used for the determination of the average neutron flux within bulky samples has been applied for the measurements of hydrogen contents of different samples. An analytical function is given for the description of the correlation between the activity of Dy foils and the hydrogen concentrations. Results obtained by the activation and the thermal neutron reflection methods are compared

  9. Elemental analysis of brazing alloy samples by neutron activation technique

    International Nuclear Information System (INIS)

    Eissa, E.A.; Rofail, N.B.; Hassan, A.M.; El-Shershaby, A.; Walley El-Dine, N.

    1996-01-01

    Two brazing alloy samples (C P 2 and C P 3 ) have been investigated by Neutron activation analysis (NAA) technique in order to identify and estimate their constituent elements. The pneumatic irradiation rabbit system (PIRS), installed at the first egyptian research reactor (ETRR-1) was used for short-time irradiation (30 s) with a thermal neutron flux of 1.6 x 10 1 1 n/cm 2 /s in the reactor reflector, where the thermal to epithermal neutron flux ratio is 106. Long-time irradiation (48 hours) was performed at reactor core periphery with thermal neutron flux of 3.34 x 10 1 2 n/cm 2 /s, and thermal to epithermal neutron flux ratio of 79. Activation by epithermal neutrons was taken into account for the (1/v) and resonance neutron absorption in both methods. A hyper pure germanium detection system was used for gamma-ray acquisitions. The concentration values of Al, Cr, Fe, Co, Cu, Zn, Se, Ag and Sb were estimated as percentages of the sample weight and compared with reported values. 1 tab

  10. Elemental analysis of brazing alloy samples by neutron activation technique

    Energy Technology Data Exchange (ETDEWEB)

    Eissa, E A; Rofail, N B; Hassan, A M [Reactor and Neutron physics Department, Nuclear Research Centre, Atomic Energy Authority, Cairo (Egypt); El-Shershaby, A; Walley El-Dine, N [Physics Department, Faculty of Girls, Ain Shams Universty, Cairo (Egypt)

    1997-12-31

    Two brazing alloy samples (C P{sup 2} and C P{sup 3}) have been investigated by Neutron activation analysis (NAA) technique in order to identify and estimate their constituent elements. The pneumatic irradiation rabbit system (PIRS), installed at the first egyptian research reactor (ETRR-1) was used for short-time irradiation (30 s) with a thermal neutron flux of 1.6 x 10{sup 1}1 n/cm{sup 2}/s in the reactor reflector, where the thermal to epithermal neutron flux ratio is 106. Long-time irradiation (48 hours) was performed at reactor core periphery with thermal neutron flux of 3.34 x 10{sup 1}2 n/cm{sup 2}/s, and thermal to epithermal neutron flux ratio of 79. Activation by epithermal neutrons was taken into account for the (1/v) and resonance neutron absorption in both methods. A hyper pure germanium detection system was used for gamma-ray acquisitions. The concentration values of Al, Cr, Fe, Co, Cu, Zn, Se, Ag and Sb were estimated as percentages of the sample weight and compared with reported values. 1 tab.

  11. Applicability of neutron activation analysis to geological samples

    Energy Technology Data Exchange (ETDEWEB)

    Ebihara, Mitsuru [Tokyo Metropolitan Univ., Graduate School of Science, Tokyo (Japan)

    2003-03-01

    The applicability of neutron activation analysis (NAA) to geological samples in space is discussed by referring to future space mission programs, by which the extraterrestrial samples are to be delivered to the earth for scientific inspections. It is concluded that both destructive and non-destructive NAA are highly effective in analyzing these samples. (author)

  12. Applicability of neutron activation analysis to geological samples

    International Nuclear Information System (INIS)

    Ebihara, Mitsuru

    2003-01-01

    The applicability of neutron activation analysis (NAA) to geological samples in space is discussed by referring to future space mission programs, by which the extraterrestrial samples are to be delivered to the earth for scientific inspections. It is concluded that both destructive and non-destructive NAA are highly effective in analyzing these samples. (author)

  13. Monte Carlo calculations and neutron spectrometry in quantitative prompt gamma neutron activation analysis (PGNAA) of bulk samples using an isotopic neutron source

    International Nuclear Information System (INIS)

    Spyrou, N.M.; Awotwi-Pratt, J.B.; Williams, A.M.

    2004-01-01

    An activation analysis facility based on an isotopic neutron source (185 GBq 241 Am/Be) which can perform both prompt and cyclic activation analysis on bulk samples, has been used for more than 20 years in many applications including 'in vivo' activation analysis and the determination of the composition of bio-environmental samples, such as, landfill waste and coal. Although the comparator method is often employed, because of the variety in shape, size and elemental composition of these bulk samples, it is often difficult and time consuming to construct appropriate comparator samples for reference. One of the obvious problems is the distribution and energy of the neutron flux in these bulk and comparator samples. In recent years, it was attempted to adopt the absolute method based on a monostandard and to make calculations using a Monte Carlo code (MCNP4C2) to explore this further. In particular, a model of the irradiation facility has been made using the MCNP4C2 code in order to investigate the factors contributing to the quantitative determination of the elemental concentrations through prompt gamma neutron activation analysis (PGNAA) and most importantly, to estimate how the neutron energy spectrum and neutron dose vary with penetration depth into the sample. This simulation is compared against the scattered and transmitted neutron energy spectra that are experimentally and empirically determined using a portable neutron spectrometry system. (author)

  14. Neutron activation analysis of certified samples by the absolute method

    Science.gov (United States)

    Kadem, F.; Belouadah, N.; Idiri, Z.

    2015-07-01

    The nuclear reactions analysis technique is mainly based on the relative method or the use of activation cross sections. In order to validate nuclear data for the calculated cross section evaluated from systematic studies, we used the neutron activation analysis technique (NAA) to determine the various constituent concentrations of certified samples for animal blood, milk and hay. In this analysis, the absolute method is used. The neutron activation technique involves irradiating the sample and subsequently performing a measurement of the activity of the sample. The fundamental equation of the activation connects several physical parameters including the cross section that is essential for the quantitative determination of the different elements composing the sample without resorting to the use of standard sample. Called the absolute method, it allows a measurement as accurate as the relative method. The results obtained by the absolute method showed that the values are as precise as the relative method requiring the use of standard sample for each element to be quantified.

  15. Large Sample Neutron Activation Analysis: A Challenge in Cultural Heritage Studies

    International Nuclear Information System (INIS)

    Stamatelatos, I.E.; Tzika, F.

    2007-01-01

    Large sample neutron activation analysis compliments and significantly extends the analytical tools available for cultural heritage and authentication studies providing unique applications of non-destructive, multi-element analysis of materials that are too precious to damage for sampling purposes, representative sampling of heterogeneous materials or even analysis of whole objects. In this work, correction factors for neutron self-shielding, gamma-ray attenuation and volume distribution of the activity in large volume samples composed of iron and ceramic material were derived. Moreover, the effect of inhomogeneity on the accuracy of the technique was examined

  16. Studies on thermal neutron perturbation factor needed for bulk sample activation analysis

    CERN Document Server

    Csikai, J; Sanami, T; Michikawa, T

    2002-01-01

    The spatial distribution of thermal neutrons produced by an Am-Be source in a graphite pile was measured via the activation foil method. The results obtained agree well with calculated data using the MCNP-4B code. A previous method used for the determination of the average neutron flux within thin absorbing samples has been improved and extended for a graphite moderator. A procedure developed for the determination of the flux perturbation factor renders the thermal neutron activation analysis of bulky samples of unknown composition possible both in hydrogenous and graphite moderators.

  17. Modern Trends in Neutron Activation Analysis. Applications to some African Environmental Samples

    International Nuclear Information System (INIS)

    Hassan, A.M.

    2009-01-01

    This review covers the results of several published articles which deal with the modern trends in neutron activation analysis techniques using some of African research reactors for some environmental samples. The samples used have been collected from different areas in Egypt, South Africa, Ghana, Morocco, Nigeria, and Algeria. The neutron irradiation facilities and the advanced detection systems in each country are outlined. The prompt and delayed gamma-rays emitted due to neutron capture have been applied for investigation of the elemental constituents of such samples. Covered applications include exploration, mining, industrial environment, pollution of air, foodstuffs, soils and irrigation water samples. Some of the developed software programmes as well as the modern methods of data analysis are presented. The thermal and epithermal neutron activation analysis techniques have been applied for estimation of major, minor and trace elements in each material. Some of these data are presented with several comments.

  18. Nondestructive neutron activation analysis of volcanic samples: Hawaii

    International Nuclear Information System (INIS)

    Zoller, W.H.; Finnegan, D.L.; Crowe, B.

    1986-01-01

    Samples of volcanic emissions have been collected between and during eruptions of both Kilauea and Mauna Loa volcanoes during the last three years. Airborne particles have been collected on Teflon filters and acidic gases on base-impregnated cellulose filters. Chemically neutral gas-phase species are collected on charcoal-coated cellulose filters. The primary analytical technique used is nondestructive neutron activation analysis, which has been used to determine the quantities of up to 35 elements on the different filters. The use of neutron activation analysis makes it possible to analyze for a wide range of elements in the different matrices used for the collection and to learn about the distribution between particles and gas phases for each of the elements

  19. Automatic sample changer for neutron activation analysis at CDTN, Brazil

    International Nuclear Information System (INIS)

    Aimore Dutra Neto; Oliveira Pelaes, Ana Clara; Jacimovic, Radojko

    2018-01-01

    An automatic sample changer was recently developed and installed in the Neutron Activation Analysis (NAA) Laboratory. The certified reference material BCR-320R, Channel Sediment, was analysed in order to verify the reliability of the results obtained by NAA, k 0 -standardisation method, using this automatic system during the gamma-ray measurement step. The results were compared to those manually obtained. The values pointed out that the automatic sample changer is working properly. This changer will increase the productiveness of the neutron activation technique applied at Nuclear Technology Development Centre, CDTN/CNEN expanding its competitiveness as an analytical technique in relation to other techniques. (author)

  20. Large sample neutron activation analysis: establishment at CDTN/CNEN, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Menezes, Maria Angela de B.C., E-mail: menezes@cdtn.b [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil); Jacimovic, Radojko, E-mail: radojko.jacimovic@ijs.s [Jozef Stefan Institute, Ljubljana (Slovenia). Dept. of Environmental Sciences. Group for Radiochemistry and Radioecology

    2011-07-01

    In order to improve the application of the neutron activation technique at CDTN/CNEN, the large sample instrumental neutron activation analysis is being established, IAEA BRA 14798 and FAPEMIG APQ-01259-09 projects. This procedure, LS-INAA, usually requires special facilities for the activation as well as for the detection. However, the TRIGA Mark I IPR R1, CDTN/CNEN has not been adapted for the irradiation and the usual gamma spectrometry has being carried out. To start the establishment of the LS-INAA, a 5g sample - IAEA/Soil 7 reference material was analyzed by k{sub 0}-standardized method. This paper is about the detector efficiency over the volume source using KayWin v2.23 and ANGLE V3.0 software. (author)

  1. Calculation of thermal neutron self-shielding correction factors for aqueous bulk sample prompt gamma neutron activation analysis using the MCNP code

    International Nuclear Information System (INIS)

    Nasrabadi, M.N.; Jalali, M.; Mohammadi, A.

    2007-01-01

    In this work thermal neutron self-shielding in aqueous bulk samples containing neutron absorbing materials is studied using bulk sample prompt gamma neutron activation analysis (BSPGNAA) with the MCNP code. The code was used to perform three dimensional simulations of a neutron source, neutron detector and sample of various material compositions. The MCNP model was validated against experimental measurements of the neutron flux performed using a BF 3 detector. Simulations were performed to predict thermal neutron self-shielding in aqueous bulk samples containing neutron absorbing solutes. In practice, the MCNP calculations are combined with experimental measurements of the relative thermal neutron flux over the sample's surface, with respect to a reference water sample, to derive the thermal neutron self-shielding within the sample. The proposed methodology can be used for the determination of the elemental concentration of unknown aqueous samples by BSPGNAA where knowledge of the average thermal neutron flux within the sample volume is required

  2. Estimated neutron-activation data for TFTR. Part II. Biological dose rate from sample-materials activation

    International Nuclear Information System (INIS)

    Ku, L.; Kolibal, J.G.

    1982-06-01

    The neutron induced material activation dose rate data are summarized for the TFTR operation. This report marks the completion of the second phase of the systematic study of the activation problem on the TFTR. The estimations of the neutron induced activation dose rates were made for spherical and slab objects, based on a point kernel method, for a wide range of materials. The dose rates as a function of cooling time for standard samples are presented for a number of typical neutron spectrum expected during TFTR DD and DT operations. The factors which account for the variations of the pulsing history, the characteristic size of the object and the distance of observation relative to the standard samples are also presented

  3. Bulk - Samples gamma-rays activation analysis (PGNAA) with Isotopic Neutron Sources

    International Nuclear Information System (INIS)

    HASSAN, A.M.

    2009-01-01

    An overview is given on research towards the Prompt Gamma-ray Neutron Activation Analysis (PGNAA) of bulk-samples. Some aspects in bulk-sample PGNAA are discussed, where irradiation by isotopic neutron sources is used mostly for in-situ or on-line analysis. The research was carried out in a comparative and/or qualitative way or by using a prior knowledge about the sample material. Sometimes we need to use the assumption that the mass fractions of all determined elements add up to 1. The sensitivity curves are also used for some elements in such complex samples, just to estimate the exact percentage concentration values. The uses of 252 Cf, 241 Arn/Be and 239 Pu/Be isotopic neutron sources for elemental investigation of: hematite, ilmenite, coal, petroleum, edible oils, phosphates and pollutant lake water samples have been mentioned.

  4. Sample design and gamma-ray counting strategy of neutron activation system for triton burnup measurements in KSTAR

    Energy Technology Data Exchange (ETDEWEB)

    Jo, Jungmin [Department of Energy System Engineering, Seoul National University, Seoul (Korea, Republic of); Cheon, Mun Seong [ITER Korea, National Fusion Research Institute, Daejeon (Korea, Republic of); Chung, Kyoung-Jae, E-mail: jkjlsh1@snu.ac.kr [Department of Energy System Engineering, Seoul National University, Seoul (Korea, Republic of); Hwang, Y.S. [Department of Energy System Engineering, Seoul National University, Seoul (Korea, Republic of)

    2016-11-01

    Highlights: • Sample design for triton burnup ratio measurement is carried out. • Samples for 14.1 MeV neutron measurements are selected for KSTAR. • Si and Cu are the most suitable materials for d-t neutron measurements. • Appropriate γ-ray counting strategies for each selected sample are established. - Abstract: On the purpose of triton burnup measurements in Korea Superconducting Tokamak Advanced Research (KSTAR) deuterium plasmas, appropriate neutron activation system (NAS) samples for 14.1 MeV d-t neutron measurements have been designed and gamma-ray counting strategy is established. Neutronics calculations are performed with the MCNP5 neutron transport code for the KSTAR neutral beam heated deuterium plasma discharges. Based on those calculations and the assumed d-t neutron yield, the activities induced by d-t neutrons are estimated with the inventory code FISPACT-2007 for candidate sample materials: Si, Cu, Al, Fe, Nb, Co, Ti, and Ni. It is found that Si, Cu, Al, and Fe are suitable for the KSATR NAS in terms of the minimum detectable activity (MDA) calculated based on the standard deviation of blank measurements. Considering background gamma-rays radiated from surrounding structures activated by thermalized fusion neutrons, appropriate gamma-ray counting strategy for each selected sample is established.

  5. Instrumental neutron activation analysis of soil sample

    International Nuclear Information System (INIS)

    Abdul Khalik Haji Wood.

    1983-01-01

    This paper describes the analysis of soil samples collected from 5 different location around Sungai Lui, Kajang, Selangor, Malaysia. These sample were taken at 22-24 cm from the top of the ground and were analysed using the techniques of Instrumental Neutron Activation Analysis (INAA). The analysis on soil sample taken above 22-24 cm level were done in order to determine if there is any variation in elemental contents at different sampling levels. The results indicate a wide variation in the contents of the samples. About 30 elements have been analysed. The major ones are Na, I, Cl, Mg, Al, K, Ti, Ca and Fe. Trace elements analysed were Ba, Sc, V, Cr, Mn, Ga, As, Zn, Br, Rb, Co, Hf, Zr, Th, U, Sb, Cs, Ce, Sm, Eu, Tb, Dy, Yb, Lu and La. (author)

  6. Radiochemical neutron activation analysis of gold in geochemical samples

    International Nuclear Information System (INIS)

    Zilliacus, R.

    1983-01-01

    A fast method for the radiochemical neutron activation analysis of gold in geochemical samples is described. The method is intended for samples having background concentrations of gold. The method is based on the dissolution of samples with hydrofluoric acid and aqua regia followed by the dissolution of the fluorides with boric acid and hydrochloric acid. Gold is then adsorbed on activated carbon by filtrating the solution through a thin carbon layer. The activity measurements are carried out using a Ge(Li)-detector and a multichannel analyzer. The chemical yields of the separation determined by reirradiation vary between 60 and 90%. The detection limit of the method is 0.2 ng/g gold in rock samples. USGS standard rocks and exploration reference materials are analyzed and the results are presented and compared with literature data. (author)

  7. Activation product analysis in a mixed sample containing both fission and neutron activation products

    Energy Technology Data Exchange (ETDEWEB)

    Morrison, Samuel S.; Clark, Sue B.; Eggemeyer, Tere A.; Finn, Erin C.; Hines, C. Corey; King, Mathew D.; Metz, Lori A.; Morley, Shannon M.; Snow, Mathew S.; Wall, Donald E.; Seiner, Brienne N.

    2017-11-02

    Activation analysis of gold (Au) is used to estimate neutron fluence resulting from a criticality event; however, such analyses are complicated by simultaneous production of other gamma-emitting fission products. Confidence in neutron fluence estimates can be increased by quantifying additional activation products such as platinum (Pt), tantalum (Ta), and tungsten (W). This work describes a radiochemical separation procedure for the determination of these activation products. Anion exchange chromatography is used to separate anionic forms of these metals in a nitric acid matrix; thiourea is used to isolate the Au and Pt fraction, followed by removal of the Ta fraction using hydrogen peroxide. W, which is not retained on the first anion exchange column, is transposed to an HCl/HF matrix to enhance retention on a second anion exchange column and finally eluted using HNO3/HF. Chemical separations result in a reduction in the minimum detectable activity by a factor of 287, 207, 141, and 471 for 182Ta, 187W, 197Pt, and 198Au respectively, with greater than 90% recovery for all elements. These results represent the highest recoveries and lowest minimum detectable activities for 182Ta, 187W, 197Pt, and 198Au from mixed fission-activation product samples to date, enabling considerable refinement in the measurement uncertainties for neutron fluences in highly complex sample matrices.

  8. Multi-element neutron activation analysis of Brazilian coal samples

    International Nuclear Information System (INIS)

    Atalla, L.T.; Requejo, C.S.

    1982-09-01

    The elements U, Th, La, Ce, Nd, Sm, Eu, Dy, Tb, Yb, Lu, Sc, Ta, Hf, Co, Ni, Cr, Mo, Ti, V, W, In, Ga, Mn, Ba, Sr, Mg, Rb, Cs, K, Cl, Br, As, Sb, Au, Ca, Al and Fe were determined in coal samples by instrumental neutron activation analysis, by using both thermal and epithermal neutron irradiations. The irradiation times were 10 minutes and 8 or 16 hours in a position where the thermal neutron flux was about 10 12 n.cm - 2 .s - 1 and 72 non-consecutive hours for epithermal irradiation at a flux of about 10 11 n.Cm - 2 .s - 1 . After the instrumental analysis of the above mentioned elements, Zn and Se were determined with chemical separation. The relative standard deviation of, at least, 4 determinations was about + - 10% for the majority of the results. The coal samples analysed were supplied by: Cia. Estadual da Tecnologia e Saneamento Basico (CETESB-SP), Cia. de Pesquisas e Lavras Minerais (COPELMI-RS), Cia. Carbonifera Urussunga (SC), Cia. Carbonifera Prospera (SC), Cia. Carbonifera Treviso (SC), Cia. Nacional de Mineracao de Carvao do Barro Branco (SC) and Comissao Nacional de Energia Nuclear (CNEN-RJ). (Author) [pt

  9. Feasibility studies on large sample neutron activation analysis using a low power research reactor

    International Nuclear Information System (INIS)

    Gyampo, O.

    2008-06-01

    Instrumental neutron activation analysis (INAA) using Ghana Research Reactor-1 (GHARR-1) can be directly applied to samples with masses in grams. Samples weights were in the range of 0.5g to 5g. Therefore, the representativity of the sample is improved as well as sensitivity. Irradiation of samples was done using a low power research reactor. The correction for the neutron self-shielding within the sample is determined from measurement of the neutron flux depression just outside the sample. Correction for gamma ray self-attenuation in the sample was performed via linear attenuation coefficients derived from transmission measurements. Quantitative and qualitative analysis of data were done using gamma ray spectrometry (HPGe detector). The results of this study on the possibilities of large sample NAA using a miniature neutron source reactor (MNSR) show clearly that the Ghana Research Reactor-1 (GHARR-1) at the National Nuclear Research Institute (NNRI) can be used for sample analyses up to 5 grams (5g) using the pneumatic transfer systems.

  10. Multi-element analysis of crude-oil samples by 14.6 MeV neutron activation

    International Nuclear Information System (INIS)

    Cam, N.F.; Cigeroglu, F.; Erduran, M.N.

    1997-01-01

    The instrumental neutron activation technique, using the SAMEST T-400 neutron generator with 14.6 MeV neutrons produced from 3 H(d,n) 4 He reaction, is demonstrated for multi-element analysis of Saudi-Arabian crude-oil samples. The system parameters for the absolute method (e.g., the counting solid-angle, intrinsic efficiency of the γ-ray detector, effective neutron flux, activation cross sections, etc.)were determined and the results of elemental concentrations were presented with the corrections for all possible interferences having been carefully considered. (author)

  11. Self-shielding coefficient and thermal flux depression factor of voluminous sample in neutron activation analysis

    International Nuclear Information System (INIS)

    Noorddin Ibrahim; Rosnie Akang

    2009-01-01

    Full text: One of the major problems encountered during the irradiation of large inhomogeneous samples in performing activation analysis using neutron is the perturbation of the neutron field due to absorption and scattering of neutron within the sample as well as along the neutron guide in the case of prompt gamma activation analysis. The magnitude of this perturbation shown by self-shielding coefficient and flux depression depend on several factors including the average neutron energy, the size and shape of the sample, as well as the macroscopic absorption cross section of the sample. In this study, we use Monte Carlo N-Particle codes to simulate the variation of neutron self-shielding coefficient and thermal flux depression factor as a function of the macroscopic thermal absorption cross section. The simulation works was carried out using the high performance computing facility available at UTM while the experimental work was performed at the tangential beam port of Reactor TRIGA PUSPATI, Malaysia Nuclear Agency. The neutron flux measured along the beam port is found to be in good agreement with the simulated data. Our simulation results also reveal that total flux perturbation factor decreases as the value of absorption increases. This factor is close to unity for low absorbing sample and tends towards zero for strong absorber. In addition, sample with long mean chord length produces smaller flux perturbation than the shorter mean chord length. When comparing both the graphs of self-shielding factor and total disturbance, we can conclude that the total disturbance of the thermal neutron flux on the large samples is dominated by the self-shielding effect. (Author)

  12. Analysis of atmospheric particulate samples via instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Greenberg, R.R.

    1990-01-01

    Instrumental neutron activation analysis (INAA) is a powerful analytical technique for the elemental characterization of atmospheric particulate samples. It is a true multielement technique with adequate sensitivity to determine 30 to 40 elements in a sample of atmospheric particulate material. Its nondestructive nature allows sample reanalysis by the same or a different analytical technique. In this paper as an example of the applicability of INAA to the study of atmospheric particulate material, a study of the emissions from municipal incinerators is described

  13. Comparison of different methods for activation analysis of geological and pedological samples: Reactor and epithermal neutron activation, relative and monostandard method

    International Nuclear Information System (INIS)

    Alian, A.; Sansoni, B.

    1980-04-01

    Using purely instrumental methods, a comparative study is presented on neutron activation analysis of rock and soil samples by whole reactor neutron spectrum and epithermal neutrons with both relative and monostandard procedures. The latter procedure used with epithermal neutron activation analysis of soil samples necessitated the use of the 'effective resonance integrals' which were determined experimentally. The incorporation of the #betta# factor, representing deviation of reactor epithermal neutron flux from 1/E law, is developed in the present work. The main criteria for the choice of one or more of the procedures studied for a given purpose are also indicated. Analysis of 15 trace elements, Ca and Fe in the standard Japanese granite JG-1 using monostandard epithermal neutron activation gave results in good agreement with the average literature values. (orig./RB) [de

  14. Neutron activation analysis of bulk samples from Chinese ancient porcelain to provenance research

    International Nuclear Information System (INIS)

    Jian Zhu; Wentao Hao; Jianming Zhen; Tongxiu Zhen; Glascock, M.D.

    2013-01-01

    Neutron activation analysis (NAA) is an important technique to determine the provenance of ancient ceramics. The most common technique used for preparing ancient samples for NAA is to grind them into a powder and then encapsulate them before neutron irradiation. Unfortunately, ceramic materials are typically very hard making it a challenge to grind them into a powder. In this study we utilize bulk porcelain samples cut from ancient shards. The bulk samples are irradiated by neutrons alongside samples that have been conventionally ground into a powder. The NAA for both the bulk samples and powders are compared and shown to provide equivalent information regarding their chemical composition. Also, the multivariate statistical have been employed to the analysis data for check the consistency. The findings suggest that NAA results are less dependent on the state of the porcelain sample, and thus bulk samples cut from shards may be used to effectively determine their provenance. (author)

  15. Multielement neutron activation analysis of underground water samples

    International Nuclear Information System (INIS)

    Kusaka, Yuzuru; Tsuji, Haruo; Fujimoto, Yuzo; Ishida, Keiko; Mamuro, Tetsuo.

    1980-01-01

    An instrumental neutron activation analysis by gamma-ray spectrometry with high resolution and large volume Ge (Li) detectors followed by data processing with an electronic computer was applied to the multielemental analysis to elucidate the chemical qualities of the underground water which has been widely used in the sake brewing industries in Mikage, Uozaki and Nishinomiya districts, called as miyamizu. The evaporated residues of the water samples were subjected to the neutron irradiations in reactor for 1 min at a thermal flux of 1.5 x 10 12 n.cm -2 .sec -1 and for 30 hrs at a thermal flux of 9.3 x 10 11 n.cm -2 .sec -1 or for 5 hrs at a thermal flux of 3.9 x 10 12 n.cm -2 .sec -1 . Thus, 11 elements in the former short irradiation and 38 elements in the latter two kinds of long irradiation can be analyzed. Conventional chemical analysis including atomic absorption method and others are also applied on the same samples, and putting the all results together, some considerations concerning the geochemical meaning of the analytical values are made. (author)

  16. Determination of mercury in biologycal samples by radiochemical neutron activation analysis

    International Nuclear Information System (INIS)

    Suc, N.V.

    1989-01-01

    The radiochemical neutron activation analysis was applied to determine contents of mercury in biological samples. Samples were digested in mixing of H 2 SO 4 and HNO 3 acid. After extraction of mercury by Ni-Ditiodietylphosphoric acid in carbontetrachloride, mercury was back extracted by 5% KI solution. Contents of mercury from five samples of fish was determined by this method. The accuracy of the method was checked by comparing it with NBS standard samples and results are good agreement

  17. A comparative study of 232Th and 238U activity estimation in soil samples by gamma spectrometry and neutron activation analysis technique

    International Nuclear Information System (INIS)

    Anilkumar, Rekha; Anilkumar, S.; Narayani, K.; Babu, D.A.R.; Sharma, D.N.

    2012-01-01

    Neutron activation analysis (NAA) is a well-established analytical technique. It has many advantages as compared to the other commonly used techniques. NAA can be performed in a variety of ways depending on the element, its activity level in the sample, interference from the sample matrix and other elements, etc. This technique is used to get high analytical sensitivity and low detection limits (ppm to ppb). The high sensitivity is due to the irradiation at high neutron flux available from the research reactors and the activity measurement is done using high resolution HPGe detectors. In this paper, the activity estimation of soil samples using neutron activation and direct gamma spectrometry methods are compared. Even though the weights of samples considered and samples preparation methods are different for these two methods, the estimated activity values are comparable. (author)

  18. Determination of gold and silver in geological standard samples MGI by instrument neutron activation analysis

    International Nuclear Information System (INIS)

    Lu Huijiuan; Zhou; Yunlu

    1987-01-01

    Gold and silver in geological standard samples MGI were determined by instrument neutron activation analysis. The various interferences of nuclides were considered. Corrected factors of the geometry in different positions have been determined. Using the geological standard sample MGM and radiochemical separation neutron activation method as reference, the reliability of this method is proved. Gold content in samples is 0.4-0.009 g/t, silver content is 9-0.3 g/t. Standard deviation is less than 3.5%, the precision of the measurement is 4.8-11.6%

  19. Neutron activation analysis of core and drill cutting samples from geothermal well drilling

    International Nuclear Information System (INIS)

    Miller, G.E.

    1986-01-01

    Samples of sandstones and shales were analysed by instrumental neutron activation analysis for a total of 30 elements. Three irradiation and five counting periods were employed. Solutions and National Bureau of Standards Reference Materials were used for comparison. The samples were obtained from drill cuttings (with a few core samples) from drillings in the Salton Sea geothermal field of California. These determinations form part of a major study to establish elemental variation as a function of mineral variation as depth and temperature in the well vary. The overall goal is to examine mineral alteration and/or element migration under typical geothermal conditions. The techniques involve typical compromises between maximizing precision for individual element determinations and the amount of time and effort that can be expended, as it is desired to examine large numbers of samples. With the limitations imposed by the reactor flux available at the U.C.Irvine TRIGA reactor, the detectors available, and time factors, most precisions are acceptable for geological comparison purposes. Some additional measurements were made by delayed-neutron counting methods to compare with uranium determinations made by conventional instrumental neutron activation analysis methods. (author)

  20. Rapid uranium analysis by delayed neutron counting of neutron activated samples

    International Nuclear Information System (INIS)

    Papadopoulos, N.N.

    1985-01-01

    The uranium analyzer at the Nuclear Research Center ''Demokritos'' and the delayed neutron method have been used to determine the uranium content in lignite, in chemically enriched samples and in solutions of extractable uranium. The results are compared with data obtained by other methods. In the case of dissolved extractable uranium. The results are in good agreement with X-ray fluorescence data in the range 100 ppm to 2000 ppm while beyond these limits the discrepancies between neutron and spectrophotometric data are observed. The results for lignite samples are in good agreement with gamma spectrometric data. Discrepancies indicate that more extensive intercomparisons are needed to check the reliability of various methods

  1. 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)

  2. Multielemental neutron activation analysis of some egyptian cement samples

    International Nuclear Information System (INIS)

    Eissa, E.A.; Rofail, N.B.; Abdel-Basset, N.; Soroor, A.; Hassan, A.M.

    1996-01-01

    Multielemental analysis of normal, Karnak and sea-water cement samples were performed by neutron activation analysis technique using the (ET-R R-1) reactor for sample irradiation. The Data were collected and analysed by means of the (HPGe) detection system and a Pca computer. A total of 23 elements namely, Na, A1, C 1, K, Ca, Sc, Cr, Mn, Fe, Co, Zn, Sr, Ba, La, Sm, Eu, Yb, Lu, Ta, Au, Th and U were identified and analysed with concentrations ranging from 1 ppm upto 62% a comparison between the elemental concentrations of the three cement types is given. 2 tabs

  3. A neutron activation detector

    International Nuclear Information System (INIS)

    Ambardanishvili, T.S.; Kolomiitsev, M.A.; Zakharina, T.Y.; Dundua, V.J.; Chikhladze, N.V.

    1973-01-01

    The present invention concerns a neutron activation detector made from a moulded and hardened composition. According to the invention, that composition contains an activable substance constituted by at least two chemical elements and/or compounds of at least two chemical elements. Each of these chemical elements is capable of reacting with the neutrons forming radio-active isotopes with vatious levels of energy during desintegration. This neutron detector is mainly suitable for measuring integral thermal neutron and fast neutron fluxes during irradiation of the sample, and also for measuring the intensities of neutron fields [fr

  4. Phosphorus analysis in milk samples by neutron activation analysis method

    International Nuclear Information System (INIS)

    Oliveira, R.M. de; Cunha, I.I.L.

    1991-01-01

    The determination of phosphorus in milk samples by instrumental thermal neutron activation analysis is described. The procedure involves a short irradiation in a nuclear reactor and measurement of the beta radiation emitted by phosphorus - 32 after a suitable decay period. The sources of error were studied and the established method was applied to standard reference materials of known phosphorus content. (author)

  5. The method of Sample Management in Neutron Activation Analysis Laboratory-Serpong

    International Nuclear Information System (INIS)

    Elisabeth-Ratnawati

    2005-01-01

    In the testing laboratory used by neutron activation analysis method, sample preparation is the main factor and it can't be neglect. The error in the sample preparation can give result with lower accuracy. In this article is explained the scheme of sample preparation i.e sample receive administration, the separate of sample, fluid and solid sample preparation, sample grouping, irradiation, sample counting and holding the sample post irradiation. If the management of samples were good application based on Standard Operation Procedure, therefore each samples has good traceability. To optimize the management of samples is needed the trained and skilled personal and good facility. (author)

  6. Determination of iodine 129 in environmental samples from Austria by neutron activation analysis

    International Nuclear Information System (INIS)

    Karg, V.; Schoenfeld, T.

    1986-11-01

    For various types of samples (thyroids from humans, from game and cows; ground water, snow and air filters) the 129 I-contents, expressed as 129 I/ 127 I-ratio (R), were determined by neutron activation analysis. The method utilises the neutron induced reactions 129 I(n, γ) 130 I and 127 I(n, 2n) 126 I. Four main steps are involved: 1. Separation of iodine from the sample and conversion to a form suitable for neutron irradiation. 2. Irradiation in a reactor. 3. Chemical processing of the irradiated material, i.e. separation of radio-iodine with addition of carrier. 4. Measurement of activities of 130 I and 126 I with a gammaspectrometer. The 129 I/ 127 I-ratio (R) is then obtained by comparing with the activities produced in a reference sample (usually with R = 1.0 x 10 -8 ) which is irradiated simultaneously. Details of the method are presented in the report. R-values between 0.6 x 10 -8 and 39 x 10 -8 were found. The highest values were those of snow and game thyroids. Ground water contained very little 129 I. The results confirm the expectation that 129 I enters the biosphere mainly via air and precipitation. (Author)

  7. Neutron-activation analysis of routine mineral-processing samples

    International Nuclear Information System (INIS)

    Watterson, J.; Eddy, B.; Pearton, D.

    1974-01-01

    Instrumental neutron-activation analysis was applied to a suite of typical mineral-processing samples to establish which elements can be rapidly determined in them by this technique. A total of 35 elements can be determined with precisions (from the counting statistics) ranging from better than 1 per cent to approximately 20 per cent. The elements that can be determined have been tabulated together with the experimental conditions, the precision from the counting statistics, and the estimated number of analyses possible per day. With an automated system, this number can be as high as 150 in the most favourable cases [af

  8. Neutron activation analysis in geological samples containing rare earths, uranium and thorium

    International Nuclear Information System (INIS)

    Vasconcellos, M.B.A.; Figueiredo, A.M.G.; Berretta, J.R.; Soares, J.C.A.C.R.; Fratin, L.; Goncales, O.L.; Botelho, S.

    1990-01-01

    The neutron activation analysis method was used for determination of rare earths, uranium, thorium and other tracks in geological samples, under the geological standard JB-1 (Geological Survey of Japan) and S-8 and S-13 (IAEA). (L.C.J.A.)

  9. Determination of sodium in biological samples by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Parwate, D.V.; Garg, A.N.

    1981-01-01

    Sodium is one of the most essential elements needed for metabolic processes amongst human beings. It is consumed in the form of sodium chloride but it is also present in edible plant leaves. Sodium is mostly analyzed by flame photometric method, a destructive and time consuming technique. Sodium has been determined in some green leave vegetables samples-palak, radish, khatta palak (ambat chuka), chaulai leaves, chauli bean covers and its seeds by instrumental neutron activation analysis. The method involves irradiation of samples with thermal neutrons from 241 Am-Be source and counting 24 Na activity (half life 15 hr) from the reaction 23 Na(n,γ) 24 Na. Activity due to 1.37 MeV photopeak was counted with a NaI(Tl) crystal coupled to gamma ray spectrometer. Green leaves of the vegetables were thoroughly washed, dried at constant temperature and powdered. Bowen's Kale powder was used as standard for measuring sodium abundances. About 2g each of samples and the standard were packed in polythene vials. They were irradiated for 24 hrs, delayed by 1 hr and then counted for 20 mts. It is found that radish leaves are most enriched in sodium (14.0 +-0.45%) amongst four leave samples analyzed. For three different parts of chaulai leaves, bean covers and seeds, sodium contents are 1.38%, 1820 and 1010 ppm. Palak contains 2.84 +-0.29% while khatta palak contains only 4210 +- 830 ppm sodium. All values reported here are for dry weight samples and are means of three replicate measurements with standard deviation. (author)

  10. Manually controlled neutron-activation system

    International Nuclear Information System (INIS)

    Johns, R.A.; Carothers, G.A.

    1982-01-01

    A manually controlled neutron activation system, the Manual Reactor Activation System, was designed and built and has been operating at one of the Savannah River Plant's production reactors. With this system, samples can be irradiated for up to 24 hours and pneumatically transferred to a shielded repository for decay until their activity is low enough for them to be handled at a radiobench. The Manual Reactor Activation System was built to provide neutron activation of solid waste forms for the Alternative Waste Forms Leach Testing Program. Neutron activation of the bulk sample prior to leaching permits sensitive multielement radiometric analyses of the leachates

  11. Assessing neutron generator output using neutron activation of silicon

    International Nuclear Information System (INIS)

    Kehayias, Pauli M.; Kehayias, Joseph J.

    2007-01-01

    D-T neutron generators are used for elemental composition analysis and medical applications. Often composition is determined by examining elemental ratios in which the knowledge of the neutron flux is unnecessary. However, the absolute value of the neutron flux is required when the generator is used for neutron activation analysis, to study radiation damage to materials, to monitor the operation of the generator, and to measure radiation exposure. We describe a method for absolute neutron output and flux measurements of low output D-T neutron generators using delayed activation of silicon. We irradiated a series of silicon oxide samples with 14.1 MeV neutrons and counted the resulting gamma rays of the 28 Al nucleus with an efficiency-calibrated detector. To minimize the photon self-absorption effects within the samples, we used a zero-thickness extrapolation technique by repeating the measurement with samples of different thicknesses. The neutron flux measured 26 cm away from the tritium target of a Thermo Electron A-325 D-T generator (Thermo Electron Corporation, Colorado Springs, CO) was 6.2 x 10 3 n/s/cm 2 ± 5%, which is consistent with the manufacturer's specifications

  12. Assessing neutron generator output using neutron activation of silicon

    Energy Technology Data Exchange (ETDEWEB)

    Kehayias, Pauli M. [Body Composition Laboratory, Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111 (United States); Kehayias, Joseph J. [Body Composition Laboratory, Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111 (United States)]. E-mail: joseph.kehayias@tufts.edu

    2007-08-15

    D-T neutron generators are used for elemental composition analysis and medical applications. Often composition is determined by examining elemental ratios in which the knowledge of the neutron flux is unnecessary. However, the absolute value of the neutron flux is required when the generator is used for neutron activation analysis, to study radiation damage to materials, to monitor the operation of the generator, and to measure radiation exposure. We describe a method for absolute neutron output and flux measurements of low output D-T neutron generators using delayed activation of silicon. We irradiated a series of silicon oxide samples with 14.1 MeV neutrons and counted the resulting gamma rays of the {sup 28}Al nucleus with an efficiency-calibrated detector. To minimize the photon self-absorption effects within the samples, we used a zero-thickness extrapolation technique by repeating the measurement with samples of different thicknesses. The neutron flux measured 26 cm away from the tritium target of a Thermo Electron A-325 D-T generator (Thermo Electron Corporation, Colorado Springs, CO) was 6.2 x 10{sup 3} n/s/cm{sup 2} {+-} 5%, which is consistent with the manufacturer's specifications.

  13. Neutron activation determination of iridium, gold, platinum, and silver in geologic samples

    International Nuclear Information System (INIS)

    Millard, H.T.

    1986-01-01

    Low-level methods for the determination of iridium and other noble metals have been important in recent years due to interest in locating abundance anomalies associated with the Cretaceous/Tertiary (K/T) boundary. Typical iridium anomalies are in the range of 1 to 100 ppb. Thus methods with detection limits near 0.1 ppb should be adequate to detect K/T boundary anomalies. Radiochemical neutron activation analysis methods continue to be required although instrumental neutron activation analysis techniques employing elaborate gamma-counters are under development. In the procedure employed in this study samples irradiated in the epithermal neutron facility of the U.S. Geological Survey TRIGA Reactor are treated with a mini-fire assay technique. The iridium, gold, and silver are collected in a 1-gram metallic lead button. Primary contaminants at this stage are arsenic and antimony. These can be removed by heating the button with a mixture of sodium peroxide and sodium hydroxide. The resulting 0.2-gram lead bead is counted in a Compton suppression spectrometer. Carrier yields are determined by reirradiation of the lead beads. This procedure has been applied to the U.S.G.S. Standard Rock PCC-1. and samples from K/T boundary sites in the Western Interior of North America. (author)

  14. Determination of phosphorus in biological samples by thermal neutron activation followed by β--counting

    International Nuclear Information System (INIS)

    Weginwar, R.G.; Samudralwar, D.L.; Garg, A.N.

    1989-01-01

    Phosphorus was determined using the β - emitter 32 P by instrumental neutron activation analysis (INAA) in several NBS and IAEA standards, and in samples of biological origin such as human and animal blood, cancerous tissue, edible plant leaves, diets, milk samples, etc. The method involves thermal neutron irradiation (for 2-10 h in a reactor) followed by β - counting on an end-window gas flow proportional counter using aluminium filter. The results are within ±10% of the certified values in most cases. (author) 29 refs.; 3 tabs

  15. Semiautomatic exchanger of samples for carry out neutron activation analysis

    International Nuclear Information System (INIS)

    Aguilar H, F.; Quintana C, G.; Torres R, C. E.; Mejia J, J. O.

    2015-09-01

    In this paper the design methodology and implementation of a semiautomatic exchanger of samples for the Analysis Laboratory by Neutron Activation of the Reactor department is presented. Taking into account the antecedents, the necessities of improvement are described, as well as the equipment that previously contained the Laboratory. The project of the semiautomatic exchanger of samples was developed at Instituto Nacional de Investigaciones Nucleares, with its own technology to increase independence from commercial equipment. Each element of the semiautomatic exchanger of samples is described both in the design phase as construction. The achieved results are positive and encouraging for the fulfillment of the proposed objective that is to increase the capacity of the Laboratory. (Author)

  16. Elemental investigation of (Al-Cu) alloys and some geological samples using neutron activation and XRF analysis techniques

    International Nuclear Information System (INIS)

    Hammad, E.A.M.

    2012-01-01

    Neutron activation analysis (NAA) using k 0 - standardization (k 0 -NAA) is well known method for multi-elemental analysis. The method is used to analyze different samples belonging to different fields. In addition, X- ray fluorescence (XRF) is also used for multi-elemental analysis. XRF complements NAA methods. Both methods were used for investigation of some iron ores and aluminum- cupper alloy (Al-Cu) samples. Elemental concentration of Iron ores and Al-Cu alloy samples were determined by k 0 - NAA and XRF methods. The iron ore samples were collected from Wadi Kareim and Umm Nar sites (the Eastern desert of Egypt). Six and two samples representing the ores of Wadi Kareim and Umm Nar, respectively altogether with the standard samples consisting of Fe, Au , Zr and W and the certified reference sample IAEA Soil-7 were irradiated in one of the irradiated boxes at the Second Egyptian Research Reactor (ETRR- 2). The induced activities were counted using an efficiency calibrated HPGe detector systems. The neutron spectrum parameters α and f characterizing the neutron irradiation position that are needed in applying k 0 -NAA method were determined using the activation product of Zr , Au, Fe and W and found α≅ - 0.048 ±0.002 and f ≅ 38± k 0 -NAA method was applied to determine the elemental concentrations in the two iron ore samples. The concentrations determined were found to vary erratically form one sample to another. The results were discussed and compared with similar results in literature. The accuracy of the k 0 - NAA method was checked by determining the elemental concentration in the IAEA-Soil 7 reference sample. The obtained results are compared with the recommended values. Good agreements were found within 10 %. Short time neutron activation analysis (STNAA) was carried out to determine concentration of major elements in Al-Cu alloy samples. Three (Al-Cu) alloys samples with different concentrations of Cu (2, 3.5 and 5 %) altogether. Au standard sample

  17. 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

  18. Investigation of an egyptian phosphate ore sample by neutron activation analysis technique

    International Nuclear Information System (INIS)

    Eissa, E.A.; Aly, R.A.; Rofail, N.B.; Hassan, A.M.

    1995-01-01

    A domestic phosphate ore sample has been analysed by means of prompt and delayed gamma-ray spectrometry following the activation by thermal neutron capture technique. The rabbit pneumatic transfer system (RPTS), long irradiation facility and two Pu/Be (2,5 Ci each) neutron sources set-Pu for prompt (n,gamma) were applied. The high purity germanium (HPGe) gamma-ray spectrometer with a personal computer analyzer (PCA) system were used for spectrum measurements. Programmes on the VAX computer were utilized for estimating the elemental concentrations of 22 out of 36 elements identified in this work. 2 tabs

  19. Neutron activation analysis for sulphur in coal samples and moisture content by gamma-ray transmission

    International Nuclear Information System (INIS)

    Selvi, S.

    1993-01-01

    A neutron activation analysis method is described for the determination of sulphur in coal samples by analysing the beta spectrum emitted from 32 P and 33 P following the reactions 32 S(n, p) 32 P and 33 S(n, p) 33 P using 252 Cf as a source of neutrons. The transmission of the combined gamma-rays emitted from three 137 Cs and three 241 Am sources is used to measure the water content of the coal samples. (author)

  20. Application of high resolution x-ray spectrometry preceded by neutron activation for elemental analysis of soil samples

    International Nuclear Information System (INIS)

    Hernandez Rivero, A.; Capote Rodriguez, G.; Padilla Alvarez, R.; Herrera Peraza, E.

    1997-01-01

    Utilization of High Resolution X-Ray Spectrometry preceded by activation of the samples by irradiation with neutron fluxes (NAA-RX) is a relatively modern trend in application of nuclear techniques. This method may complement advantageously the usual Neutron Activation Analysis by means of Gamma Spectrometry (NAA-G). In this work results obtained by the application of NAA-RX for non-destructive analysis of Cuban soil samples are discussed. The samples were irradiated with reactor neutron fluxes and the induced characteristic X-rays were measured by using Si(Li)-detector. Concentrations of Fe, Zn and Eu as determined by NAA-RX are compared with both NAA-G and XRF data. For the elaboration of X-Ray and Gamma Spectra the computer programs AXIL and ACTAN were used respectively. (author) [es

  1. Application of high resolution x-ray spectrometry preceded by neutron activation for elemental analysis of soil samples

    International Nuclear Information System (INIS)

    Hernandez Rivero, A.; Capote Rodriguez, G.; Herrera Peraza, E.

    1996-01-01

    Utilization of High Resolution X-Ray Spectrometry preceded by activation of the samples by irradiation with neutron fluxes (NAA R X) is a relatively modern trend in application of nuclear techniques. This method may complement advantageously the usual Neutron Activation Analysis by means of Gamma Spectrometry (NAA-G) In this work results obtained by the application of NAA-RX for non-destructive analysis of Cuban soil samples are discussed. The samples were irradiated with reactor neutron fluxes and the induced characteristic X-rays were measured by using Si(li)-detector. Concentrations of Fe, Zn and Eu as determined by NAA-RX are compared with both NAA-G and XRF data. For the elaboration of X-ray and Gamma Spectra the computer programs AXIL and ACTAN were used respectively

  2. Analysis by neutronic activation of samples of a geologic formation of Cuba

    International Nuclear Information System (INIS)

    Capote Rodriguez, G.; Pena Fortes, B.; Padilla Alvarez, R.; Llanes Castro, A.I.; Perez Zayas, G.; Hernandez Rivero, A.T.; Lopez Reyes, M. C.; Ribeiro Guevara, S.; Molina Insfran, J.

    1997-01-01

    The analysis by neutronic activation (AAN) is an analytical non destructive technique of high accuracy and sensibility. These advantages are very utilized in the determination of geological multielemental samples. In the job 22 elements are determined in 9 geological samples pertaining to the complex of dams of acid composition that includes the graphitic micaceous schist and the quartzites of the Canada Formation, developed fundamentally in the fasteners of the anticlinal Victoria (Yac. of Wolframio Lela, Island of the Youth, Cuba) The results obtained are of great importance for the evaluation of the potentiality of these rocks as fountains or of uranium adjusting and for the geologic prognostic of the region in study. The irradiation of the samples was carried out during three campaigns, in two occasions (October 1992 and November 1994) in the reactor of investigations of the ININ of Mexico, with a flow of thermic neutrons of 10a the 13 n.s -1 cm -2 and in an occasion in the nuclear reactor of the CAB (september 1994), with a flow of thermic neutrons of 6x 10 to the 12 n.s-1. The results were processed with the program ACTAM in the CEADEN. (S. Grainger) [es

  3. Determination of the neutron activation profile of core drill samples by gamma-ray spectrometry.

    Science.gov (United States)

    Gurau, D; Boden, S; Sima, O; Stanga, D

    2018-04-01

    This paper provides guidance for determining the neutron activation profile of core drill samples taken from the biological shield of nuclear reactors using gamma spectrometry measurements. Thus, it provides guidance for selecting a model of the right form to fit data and using least squares methods for model fitting. The activity profiles of two core samples taken from the biological shield of a nuclear reactor were determined. The effective activation depth and the total activity of core samples along with their uncertainties were computed by Monte Carlo simulation. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Limitations for qualitative and quantitative neutron activation analysis using reactor neutrons

    International Nuclear Information System (INIS)

    El-Abbady, W.H.; El-Tanahy, Z.H.; El-Hagg, A.A.; Hassan, A.M.

    1999-01-01

    In this work, the most important limitations for qualitative and quantitative analysis using reactor neutrons for activation are reviewed. Each limitation is discussed using different examples of activated samples. Photopeak estimation, nuclear reactions interference and neutron flux measurements are taken into consideration. Solutions for high accuracy evaluation in neutron activation analysis applications are given. (author)

  5. Neutron activation analysis at the Californium User Facility for Neutron Science

    International Nuclear Information System (INIS)

    Martin, R.C.; Smith, E.H.; Glasgow, D.C.; Jerde, E.A.; Marsh, D.L.; Zhao, L.

    1997-12-01

    The Californium User Facility (CUF) for Neutron Science has been established to provide 252 Cf-based neutron irradiation services and research capabilities including neutron activation analysis (NAA). A major advantage of the CUF is its accessibility and controlled experimental conditions compared with those of a reactor environment The CUF maintains the world's largest inventory of compact 252 Cf neutron sources. Neutron source intensities of ≤ 10 11 neutrons/s are available for irradiations within a contamination-free hot cell, capable of providing thermal and fast neutron fluxes exceeding 10 8 cm -2 s -1 at the sample. Total flux of ≥10 9 cm -2 s -1 is feasible for large-volume irradiation rabbits within the 252 Cf storage pool. Neutron and gamma transport calculations have been performed using the Monte Carlo transport code MCNP to estimate irradiation fluxes available for sample activation within the hot cell and storage pool and to design and optimize a prompt gamma NAA (PGNAA) configuration for large sample volumes. Confirmatory NAA irradiations have been performed within the pool. Gamma spectroscopy capabilities including PGNAA are being established within the CUF for sample analysis

  6. Enhanced NIF neutron activation diagnostics.

    Science.gov (United States)

    Yeamans, C B; Bleuel, D L; Bernstein, L A

    2012-10-01

    The NIF neutron activation diagnostic suite relies on removable activation samples, leading to operational inefficiencies and a fundamental lower limit on the half-life of the activated product that can be observed. A neutron diagnostic system measuring activation of permanently installed samples could remove these limitations and significantly enhance overall neutron diagnostic capabilities. The physics and engineering aspects of two proposed systems are considered: one measuring the (89)Zr/(89 m)Zr isomer ratio in the existing Zr activation medium and the other using potassium zirconate as the activation medium. Both proposed systems could improve the signal-to-noise ratio of the current system by at least a factor of 5 and would allow independent measurement of fusion core velocity and fuel areal density.

  7. Elemental analysis of soil and hair sample by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Chung, Yong Sam; Quraishi, Shamshad Begum; Moon, Jong Hwa; Kim, Sun Ha; Baek, Sung Yeoil; Kang, Sang Hoon; Lim, Jong Myoung; Cho, Hyun Je; Kim, Young Jin

    2004-03-01

    Myanmar soil sample was analyzed by using the instrumental neutron activation analysis. The elemental concentrations in the sample, altogether 34 elements, Al As, Ba, Ce, Co, Cr, Cs, Eu, Fe, Ga, Gd, Hf, Ir, K, La, Lu, Mn, Na, Nd, Rb, Sb, Sc, Se, Sm, Th, Ti, V, Yb, Zn and Zr were determined. The concentration of 17 elements (Al, Au, Br, Ca, Cl, Cr, Cu, Co, Fe, Hg, K, Na, Mn, Mg, Sb, Se, Zn) in human hair samples were determined by INAA For quality control of analytical method, certified reference material was used

  8. Elemental analysis of soil and hair sample by instrumental neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Chung, Yong Sam; Quraishi, Shamshad Begum; Moon, Jong Hwa; Kim, Sun Ha; Baek, Sung Yeoil; Kang, Sang Hoon; Lim, Jong Myoung; Cho, Hyun Je; Kim, Young Jin

    2004-03-01

    Myanmar soil sample was analyzed by using the instrumental neutron activation analysis. The elemental concentrations in the sample, altogether 34 elements, Al As, Ba, Ce, Co, Cr, Cs, Eu, Fe, Ga, Gd, Hf, Ir, K, La, Lu, Mn, Na, Nd, Rb, Sb, Sc, Se, Sm, Th, Ti, V, Yb, Zn and Zr were determined. The concentration of 17 elements (Al, Au, Br, Ca, Cl, Cr, Cu, Co, Fe, Hg, K, Na, Mn, Mg, Sb, Se, Zn) in human hair samples were determined by INAA For quality control of analytical method, certified reference material was used.

  9. Uncertainty Estimation of Neutron Activation Analysis in Zinc Elemental Determination in Food Samples

    International Nuclear Information System (INIS)

    Endah Damastuti; Muhayatun; Diah Dwiana L

    2009-01-01

    Beside to complished the requirements of international standard of ISO/IEC 17025:2005, uncertainty estimation should be done to increase quality and confidence of analysis results and also to establish traceability of the analysis results to SI unit. Neutron activation analysis is a major technique used by Radiometry technique analysis laboratory and is included as scope of accreditation under ISO/IEC 17025:2005, therefore uncertainty estimation of neutron activation analysis is needed to be carried out. Sample and standard preparation as well as, irradiation and measurement using gamma spectrometry were the main activities which could give contribution to uncertainty. The components of uncertainty sources were specifically explained. The result of expanded uncertainty was 4,0 mg/kg with level of confidence 95% (coverage factor=2) and Zn concentration was 25,1 mg/kg. Counting statistic of cuplikan and standard were the major contribution of combined uncertainty. The uncertainty estimation was expected to increase the quality of the analysis results and could be applied further to other kind of samples. (author)

  10. Neutron activation analysis of wheat samples

    International Nuclear Information System (INIS)

    Galinha, C.; Anawar, H.M.; Freitas, M.C.; Pacheco, A.M.G.; Almeida-Silva, M.; Coutinho, J.; Macas, B.; Almeida, A.S.

    2011-01-01

    The deficiency of essential micronutrients and excess of toxic metals in cereals, an important food items for human nutrition, can cause public health risk. Therefore, before their consumption and adoption of soil supplementation, concentrations of essential micronutrients and metals in cereals should be monitored. This study collected soil and two varieties of wheat samples-Triticum aestivum L. (Jordao/bread wheat), and Triticum durum L. (Marialva/durum wheat) from Elvas area, Portugal and analyzed concentrations of As, Cr, Co, Fe, K, Na, Rb and Zn using Instrumental Neutron Activation Analysis (INAA) to focus on the risk of adverse public health issues. The low variability and moderate concentrations of metals in soils indicated a lower significant effect of environmental input on metal concentrations in agricultural soils. The Cr and Fe concentrations in soils that ranged from 93-117 and 26,400-31,300 mg/kg, respectively, were relatively high, but Zn concentration was very low (below detection limit Fe>Na>Zn>Cr>Rb>As>Co. Concentrations of As, Co and Cr in root, straw and spike of both varieties were higher than the permissible limits with exception of a few samples. The concentrations of Zn in root, straw and spike were relatively low (4-30 mg/kg) indicating the deficiency of an essential micronutrient Zn in wheat cultivated in Portugal. The elemental transfer from soil to plant decreases with increasing growth of the plant. The concentrations of various metals in different parts of wheat followed the order: Root>Straw>Spike. A few root, straw and spike samples showed enrichment of metals, but the majority of the samples showed no enrichment. Potassium is enriched in all samples of root, straw and spike for both varieties of wheat. Relatively to the seed used for cultivation, Jordao presented higher transfer coefficients than Marialva, in particular for Co, Fe, and Na. The Jordao and Marialva cultivars accumulated not statistically significant different

  11. Development of high flux thermal neutron generator for neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Vainionpaa, Jaakko H., E-mail: hannes@adelphitech.com [Adelphi Technology, 2003 E Bayshore Rd, Redwood City, CA 94063 (United States); Chen, Allan X.; Piestrup, Melvin A.; Gary, Charles K. [Adelphi Technology, 2003 E Bayshore Rd, Redwood City, CA 94063 (United States); Jones, Glenn [G& J Jones Enterprice, 7486 Brighton Ct, Dublin, CA 94568 (United States); Pantell, Richard H. [Department of Electrical Engineering, Stanford University, Stanford, CA (United States)

    2015-05-01

    The new model DD110MB neutron generator from Adelphi Technology produces thermal (<0.5 eV) neutron flux that is normally achieved in a nuclear reactor or larger accelerator based systems. Thermal neutron fluxes of 3–5 · 10{sup 7} n/cm{sup 2}/s are measured. This flux is achieved using four ion beams arranged concentrically around a target chamber containing a compact moderator with a central sample cylinder. Fast neutron yield of ∼2 · 10{sup 10} n/s is created at the titanium surface of the target chamber. The thickness and material of the moderator is selected to maximize the thermal neutron flux at the center. The 2.5 MeV neutrons are quickly thermalized to energies below 0.5 eV and concentrated at the sample cylinder. The maximum flux of thermal neutrons at the target is achieved when approximately half of the neutrons at the sample area are thermalized. In this paper we present simulation results used to characterize performance of the neutron generator. The neutron flux can be used for neutron activation analysis (NAA) prompt gamma neutron activation analysis (PGNAA) for determining the concentrations of elements in many materials. Another envisioned use of the generator is production of radioactive isotopes. DD110MB is small enough for modest-sized laboratories and universities. Compared to nuclear reactors the DD110MB produces comparable thermal flux but provides reduced administrative and safety requirements and it can be run in pulsed mode, which is beneficial in many neutron activation techniques.

  12. Determination of uranium and thorium in rock samples from Harargaj Anticline by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Rahman, M.; Molla, N.I.; Sharif, A.K.M.; Basunia, S.; Islam, S.; Miah, R.U.; Hossain, S.M.; Chowdhury, M.I.; Bhuiyan, A.D.; Stegnar, P.

    1993-01-01

    Uranium and thorium were determined in geological materials such as radioactive rock samples collected from the Harargaj Anticline in Moulavi Bazar. The pure instrumental neutron activation analysis (INAA) technique was used in qualitative and quantitative analysis of the rock samples for U and Th. The samples were properly prepared together with their standards and simultaneously irradiated in a neutron flux of the order of 10 12 n*cm -2 *s -1 using the TRIGA MARK II research reactor facility at the AERE, Savar, Dhaka. After activation the samples were subjected to γ-ray spectrometry using a high purity germanium detection system. As a result of the analysis, U and Th could be determined. The data are consistent with the values reported by the ground radiometric survey group for some of the samples. (author) 7 refs.; 1 fig.; 2 tabs

  13. Development of Cold Neutron Activation Station at HANARO Cold Neutron Source

    International Nuclear Information System (INIS)

    Sun, G. M.; Hoang, S. M. T.; Moon, J. H.; Chung, Y. S.; Cho, S. J.; Lee, K. H.; Park, B. G.; Choi, H. D.

    2012-01-01

    A new cold neutron source at the HANARO Research Reactor had been constructed in the framework of a five-year project, and ended in 2009. It has seven neutron guides, among which five guides were already allocated for a number of neutron scattering instruments. A new two-year project to develop a Cold Neutron Activation Station (CONAS) was carried out at the two neutron guides since May 2010, which was supported by the program of the Ministry of Education, Science and Technology, Korea. Fig. 1 shows the location of CONAS. CONAS is a complex facility including several radioanalytical instruments utilizing neutron capture reaction to analyze elements in a sample. It was designed to include three instruments like a CN-PGAA (Cold Neutron - Prompt Gamma Activation Analysis), a CN-NIPS (Cold Neutron - Neutron Induced Pair Spectrometer), and a CN-NDP (Cold Neutron - Neutron-induced prompt charged particle Depth Profiling). Fig. 2 shows the conceptual configuration of the CONAS concrete bioshield and the instruments. CN-PGAA and CN-NIPS measure the gamma-rays promptly emitted from the sample after neutron capture, whereas CN-NDP is a probe to measure the charged particles emitted from the sample surface after neutron capture. For this, we constructed two cold neutron guides called CG1 and CG2B guides from the CNS

  14. Trace aluminium determination and sampling problems of archeological bone employing destructive neutron activation analysis

    International Nuclear Information System (INIS)

    Blotcky, A.J.; Rack, E.P.; Recker, R.R.; Leffler, J.A.; Teitelbaum, S.

    1978-01-01

    A destructive neutron activation analysis procedure was developed for determining trace aluminium content in bone. The method is based on a carefully planned sample preparation, irradiation at a neutron flux for 3.1x10 11 nxcm -2 xs -1 for 5 minutes, and chemical separation based on ion exchange. It was found that bone samples soaked in aluminium containing soil gave highly elevated aluminium values as a result of the aluminium adsorption into the bone matrix. The maximum aluminium content values for prehistoric bones are larger than those of modern bones and comparable to aluminium levels present in bone from renal patients. (T.G.)

  15. Analysis of some Egyptian cosmetic samples by fast neutron activation analysis

    International Nuclear Information System (INIS)

    Medhat, M.E.; Ali, M.A.; Hassan, M.F.

    2001-01-01

    A description of D-T neutron generator (NG) is presented. This generator can be used for fast neutron activation analysis applied to determine some selected elements, especially light elements, in different materials. The concentrations of the elements Na, Mg, Al, Si, K, Cl, Ca and Fe were determined in two domestic brands of face powder by using 14 MeV neutron activation analysis

  16. Instrumental neutron activation analysis of rib bone samples and of bone reference materials

    International Nuclear Information System (INIS)

    Saiki, M.; Takata, M.K.; Kramarski, S.; Borelli, A.

    2000-01-01

    The instrumental neutron activation analysis method was used for the determination of trace elements in rib bone samples taken from autopsies of accident victims. The elements Br, Ca, Cl, Cr, Fe, Mg, Mn, Na, P, Sr, Rb and Zn were determined in cortical tissues by using short and long irradiations with thermal neutron flux of the IEA-R1m nuclear reactor. The reference materials NIST SRM 1400 Bone Ash and NIST SRM 1486 Bone Meal were also analyzed in order to evaluate the precision and the accuracy of the results. It was verified that lyophilization is the most convenient process for drying bone samples since it does not cause any element losses. Comparisons were made between the results obtained for rib samples and the literature values as well as between the results obtained for different ribs from a single individual and for bones from different individuals. (author)

  17. Analysis of Some Egyptian Cosmetic Samples by Fast Neutron Activation Analysis

    CERN Document Server

    Medhat, M E; Fayez-Hassan, M

    2001-01-01

    A description of D-T neutron generator (NG) is presented. This generator can be used for fast neutron activation analysis applied to determine some selected elements, especially light elements, in different materials. In our work, the concentration of the elements Na, Mg, Al, Si, K, Cl, Ca and Fe, were determined in two domestic brands of face powder by using 14 MeV neutron activation analysis.

  18. Determination of selenium in food matrices by replicate sample neutron activation analysis

    International Nuclear Information System (INIS)

    Ventura, M.G.; Freitas, M.C.; Ventura, M.G.; Pacheco, A.M.G.

    2009-01-01

    The replicate sample instrumental neutron activation method was optimized and used for the determination of selenium in foodstuffs. The method was reliable, yielding accurate results. Lower detections limits were obtained after each successive irradiation. Different irradiation conditions were used depending on the type of sample. For samples with higher selenium contents (meat, fish, eggs), the measured selenium in the first replicate is in all cases larger than the detection limit, but a better accuracy was obtained with a larger number of replicates (2-3 replicates). For samples with extremely low selenium contents (vegetable samples), at least seven replicates were necessary to obtain a concentration value two times larger than the detection limit. (author)

  19. Neutron activation determination of impurities in molybdenum

    International Nuclear Information System (INIS)

    Usmanova, M.M.; Mukhamedshina, N.M.; Obraztsova, T.V.; Saidakhmedov, K.Kh.

    1984-01-01

    Instrumental neutron-activation techniques of impurity element determination in molybdenum and MoO 3 (solid and powdered samples) have been developed. When determining impurities of Na, K, Mn, Cu, W, Re molybdenum has been irradiated by thermal neutrons in reactor for 20 min, the sample mass constituted 200-300 mg, sample cooling time after irradiation - 2.5-3.5 h. It is shown that in the process of Cr, Fe, Co, Zn determination the samples should be irradiated with thermal neutrons, and in the process of Sb, Ta and Ni determination - with resonance and fast neutrons. Simultaneous determination of the elements during irradiation with neutrons with reactor spectrum is possible. When determining P and S the samples are irradiated with thermal and epithermal neutrons and β-activity of samples and comparison samples are measured using β-spectrometer with anthracene crystal. The techniques developed permit to determine impurities in Mo with a relative standard deviation 0.07-0.15 and lower boundaries of contents determined - 10 -4 - 10 -7 %

  20. Neutron-induced {sup 63}Ni activity and microscopic observation of copper samples exposed to the Hiroshima atomic bomb

    Energy Technology Data Exchange (ETDEWEB)

    Shizuma, Kiyoshi, E-mail: shizuma@hiroshima-u.ac.jp [Quantum Energy Applications, Department of Mechanical Science and Engineering, Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527 (Japan); Endo, Satoru [Quantum Energy Applications, Department of Mechanical Science and Engineering, Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527 (Japan); Shinozaki, Kenji [Materials Joining Science and Engineering, Department of Mechanical Science and Engineering, Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527 (Japan); Fukushima, Hiroshi [Materials Physics, Department of Mechanical Science and Engineering, Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527 (Japan)

    2013-05-01

    Fast neutron activation data for {sup 63}Ni in copper samples exposed to the Hiroshima atomic bomb are important in evaluating neutron doses to the survivors. Up to until now, accelerator mass spectrometry and liquid scintillation counting methods have been applied in {sup 63}Ni measurements and data were accumulated within 1500 m from the hypocenter. The slope of the activation curve versus distance shows reasonable agreement with the calculation result, however, data near the hypocenter are scarce. In the present work, two copper samples obtained from the Atomic bomb dome (155 m from the hypocenter) and the Bank of Japan building (392 m) were utilized in {sup 63}Ni beta-ray measurement with a Si surface barrier detector. Additionally, microscopic observation of the metal surfaces was performed for the first time. Only upper limit of {sup 63}Ni production was obtained for copper sample of the Atomic bomb dome. The result of the {sup 63}Ni measurement for Bank of Japan building show reasonable agreement with the AMS measurement and to fast neutron activation calculations based on the Dosimetry System 2002 (DS02) neutrons.

  1. Determination of Iron and Nickel in Geological Samples by Activation Analysis with Reactor Fast Neutrons

    International Nuclear Information System (INIS)

    El Abd, A.

    2009-01-01

    Threshold reactions induced by reactor fast neutrons are well recognized. The concentration of Fe and Ni were determined in nine geological samples by activation analysis with reactor fast neutrons using the threshold reactions 5 4F e( n,p) 54 Mn and 58 Ni ( n, p )'5 8 Co respectively. The fast neutron flux was determined using the reactions 92 Mo(n, 2n) 92 mNb and 95 Mo(n,p) 95 Nb. The determined concentration of Fe and Ni in the samples were checked by determining them in the GSJ JB-1 reference material using the same , ( p, n) reactions. There are a good agreement between the measured and recommended values. The concentrations of Fe were also determined by the ) , ( n, γ) capture reactions in the geological samples and the JB-1 reference material using the K θ - NAA method. There are good agreements between the determined concentrations from the ) , ( p, n) and the ( γ, n) reactions.

  2. Determination of uranium in tree bark samples by epithermal neutron activation analysis

    International Nuclear Information System (INIS)

    Lima, Nicole Pereira de; Saiki, Mitiko

    2017-01-01

    In this study uranium (U) concentrations were determined in certified reference materials (CRMs) and in tree bark samples collected in 'Cidade Universitaria Armando de Salles Oliveira' (CUASO) USP, Sao Paulo, SP, Brazil). The barks were collected from different species namely Poincianella pluviosa and Tipuana tipu. These bark samples were cleaned, dried, grated and milled for the analyses by epithermal neutron activation analysis method (ENAA). This method consists on irradiating samples and U standard in IEAR1 nuclear reactor with thermal neutron flux of 1:9 x 10 12 n cm -2 s -1 during 40 to 60 seconds depending on the samples matrices. The samples and standard were measured by gamma ray spectroscopy. U was identified by the peak of 74.66 keV of 239 U with half life of 23.47 minutes. Concentration of U was calculated by comparative method. For analytical quality control of U results, certified reference materials were analysed. Results obtained for CRMs presented good precision and accuracy, with |Z score| <= 0.39. Uranium concentrations in tree barks varied from 83.1 to 627.6 ng g - 1 and the relative standard deviations of these results ranged from 1.8 to 10%. (author)

  3. Determination of uranium in tree bark samples by epithermal neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Lima, Nicole Pereira de; Saiki, Mitiko, E-mail: mitiko@ipen.com [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2017-11-01

    In this study uranium (U) concentrations were determined in certified reference materials (CRMs) and in tree bark samples collected in 'Cidade Universitaria Armando de Salles Oliveira' (CUASO) USP, Sao Paulo, SP, Brazil). The barks were collected from different species namely Poincianella pluviosa and Tipuana tipu. These bark samples were cleaned, dried, grated and milled for the analyses by epithermal neutron activation analysis method (ENAA). This method consists on irradiating samples and U standard in IEAR1 nuclear reactor with thermal neutron flux of 1:9 x 10{sup 12} n cm{sup -2} s{sup -1} during 40 to 60 seconds depending on the samples matrices. The samples and standard were measured by gamma ray spectroscopy. U was identified by the peak of 74.66 keV of {sup 239}U with half life of 23.47 minutes. Concentration of U was calculated by comparative method. For analytical quality control of U results, certified reference materials were analysed. Results obtained for CRMs presented good precision and accuracy, with |Z score| <= 0.39. Uranium concentrations in tree barks varied from 83.1 to 627.6 ng g{sup -} {sup 1} and the relative standard deviations of these results ranged from 1.8 to 10%. (author)

  4. Multielemental determination in Citrus spp bee honey samples by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Favaro, D.I.T.; Vasconcellos, M.B.A.; Pamplona, B.

    1990-07-01

    Recently interest has grown in the determination of the concentration of inorganic chemical elements in honey bee samples, due its utilization as indicator of environmental pollution in several countries of Europe. In the present work, a method was developed to determine some essential and potentially inorganic elements in honey bee samples by intrumental neutrons activation analysis followed by high resolution gamma ray spectrometry. The honey samples were neutron irradiated during differents times at the nuclear research reactor IEA-Rl of the IPEN-CNEN/SP. The elements Na, Cl, K, Mg and Mn were determined using irradiations of 30 minutes under a thermal neutron flux of 10 12 n.cm -2 .s -1 . With 16 hours of irradiation under a flux of 10 13 n.cm -2 .s -1 and different cooling times, the elements Br, Ca, Au, Sb, Cs, Rb, Zn, Sc, Fe, Co and La were determined. The concentration of the analyzed elements ranged from ng/g to mg/g. In the future, different kinds of bee honey will be analyzed and the characteristic chemical composition of each one will be established. Based on these elemental concentration data, the relationship between the mineral composition of bee honey and its geographical origin can be studied. (author) [pt

  5. Determination of iodine in biological samples by neutron activation analysis (NAA)

    International Nuclear Information System (INIS)

    Geetha, P.V.; Karunakara, N.; Prabhu, Ujwal; Yashodhara, I.; Ravi, P.M.; Sudhakar, J.; Ajith, Nicy; Swain, K.K.; Verma, R.; Reddy, A.V.R.; Acharya, R.

    2010-01-01

    During normal operating conditions of a nuclear reactor, the release of radionuclides to the environment will be extremely low and well within the limits. Radioiodine ( 131 I) is one of the radionuclides likely to get released into the atmosphere in case of a reactor accident. During the short initial phase of release of radioactivity, 131 I is rapidly transferred to milk, leading to significant thyroid dose to those consuming milk, especially infant and children. Hence, studies on Iodine transfer through grass-cow-milk is very important. Extensive studies on transfer for 131 I through grass-cow-milk pathway after Chernobyl accident has been reported. But, under normal operational conditions of the power reactor, 131 I is not present in measurable concentration in environmental matrices of a nuclear power generating station. Stable iodine is present in all environmental samples and from the concentration of stable iodine in grass and milk, one can estimate the transfer factor. The measurement of stable iodine in environmental sample is very challenging because of its extremely low concentration. Neutron activation analysis can be used for estimation of stable iodine in the environment after suitably optimizing the condition to minimize interferences. A method has been developed based on thermal neutron activation analysis (NAA) to estimate the iodine concentration present in grass and cow milk

  6. Development of Large Sample Neutron Activation Technique for New Applications in Thailand

    International Nuclear Information System (INIS)

    Laoharojanaphand, S.; Tippayakul, C.; Wonglee, S.; Channuie, J.

    2018-01-01

    The development of the Large Sample Neutron Activation Analysis (LSNAA) in Thailand is presented in this paper. The technique had been firstly developed with rice sample as the test subject. The Thai Research Reactor-1/Modification 1 (TRR-1/M1) was used as the neutron source. The first step was to select and characterize an appropriate irradiation facility for the research. An out-core irradiation facility (A4 position) was first attempted. The results performed with the A4 facility were then used as guides for the subsequent experiments with the thermal column facility. The characterization of the thermal column was performed with Cu-wire to determine spatial distribution without and with rice sample. The flux depression without rice sample was observed to be less than 30% while the flux depression with rice sample increased to within 60%. The flux monitors internal to the rice sample were used to determine average flux over the rice sample. The gamma selfshielding effect during gamma measurement was corrected using the Monte Carlo simulation. The ratio between the efficiencies of the volume source and the point source for each energy point was calculated by the MCNPX code. The research team adopted the k0-NAA methodology to calculate the element concentration in the research. The k0-NAA program which developed by IAEA was set up to simulate the conditions of the irradiation and measurement facilities used in this research. The element concentrations in the bulk rice sample were then calculated taking into account the flux depression and gamma efficiency corrections. At the moment, the results still show large discrepancies with the reference values. However, more research on the validation will be performed to identify sources of errors. Moreover, this LS-NAA technique was introduced for the activation analysis of the IAEA archaeological mock-up. The results are provided in this report. (author)

  7. Epiboron instrumental neutron activation analysis for the determination of iodine in various salt samples

    International Nuclear Information System (INIS)

    Nyarko, B.J.B.; Serfor-Armah, Y.; Osae, S.; Akaho, E.H.K.; Anim-Sampong, S.; Maakuu, B.T.

    2001-01-01

    Epiboron instrumental neutron activation analysis (EINAA) using flexible boron as thermal neutron filter, has been used to analyze several salt samples obtained from various markets in Ghana for iodine. The method involves the irradiation of samples in boron carbide-lined polyethylene vials at the outer irradiation site of the Ghana Research Reactor-1 (GHARR-1). The samples were then counted directly without any pre-treatment on a Canberra N-type HPGe detector. The qualitative and quantitative analyses were done using the 443 keV photopeak of 128 I. The precision and accuracy of the method have been evaluated and the detection limits of the various samples were calculated. The values of iodine determined in the iodized salt range between 10.0 and 210 ppm. For non-iodinated salts, iodine levels were below 500 ppb. The values obtained show great variations among the salt samples, sample collection time and from market to market. This results show that the method can be successfully applied in the determination of trace amount of iodine in salt samples without any chemical separation. (author)

  8. Neutron activation analysis of wheat samples

    Energy Technology Data Exchange (ETDEWEB)

    Galinha, C. [CERENA-IST, Technical University of Lisbon, Av. Rovisco Pais 1, 1049-001 Lisboa (Portugal); Instituto Tecnoclogico e Nuclear, URSN, E.N. 10, 2686-953 Sacavem (Portugal); Anawar, H.M. [Instituto Tecnoclogico e Nuclear, URSN, E.N. 10, 2686-953 Sacavem (Portugal); Freitas, M.C., E-mail: cfreitas@itn.pt [Instituto Tecnoclogico e Nuclear, URSN, E.N. 10, 2686-953 Sacavem (Portugal); Pacheco, A.M.G. [CERENA-IST, Technical University of Lisbon, Av. Rovisco Pais 1, 1049-001 Lisboa (Portugal); Almeida-Silva, M. [Instituto Tecnoclogico e Nuclear, URSN, E.N. 10, 2686-953 Sacavem (Portugal); Coutinho, J.; Macas, B.; Almeida, A.S. [INRB/INIA-Elvas, National Institute of Biological Resources, Est. Gil Vaz, 7350-228 Elvas (Portugal)

    2011-11-15

    The deficiency of essential micronutrients and excess of toxic metals in cereals, an important food items for human nutrition, can cause public health risk. Therefore, before their consumption and adoption of soil supplementation, concentrations of essential micronutrients and metals in cereals should be monitored. This study collected soil and two varieties of wheat samples-Triticum aestivum L. (Jordao/bread wheat), and Triticum durum L. (Marialva/durum wheat) from Elvas area, Portugal and analyzed concentrations of As, Cr, Co, Fe, K, Na, Rb and Zn using Instrumental Neutron Activation Analysis (INAA) to focus on the risk of adverse public health issues. The low variability and moderate concentrations of metals in soils indicated a lower significant effect of environmental input on metal concentrations in agricultural soils. The Cr and Fe concentrations in soils that ranged from 93-117 and 26,400-31,300 mg/kg, respectively, were relatively high, but Zn concentration was very low (below detection limit <22 mg/kg) indicating that soils should be supplemented with Zn during cultivation. The concentrations of metals in roots and straw of both varieties of wheat decreased in the order of K>Fe>Na>Zn>Cr>Rb>As>Co. Concentrations of As, Co and Cr in root, straw and spike of both varieties were higher than the permissible limits with exception of a few samples. The concentrations of Zn in root, straw and spike were relatively low (4-30 mg/kg) indicating the deficiency of an essential micronutrient Zn in wheat cultivated in Portugal. The elemental transfer from soil to plant decreases with increasing growth of the plant. The concentrations of various metals in different parts of wheat followed the order: Root>Straw>Spike. A few root, straw and spike samples showed enrichment of metals, but the majority of the samples showed no enrichment. Potassium is enriched in all samples of root, straw and spike for both varieties of wheat. Relatively to the seed used for cultivation

  9. Non destructive multi elemental analysis using prompt gamma neutron activation analysis techniques: Preliminary results for concrete sample

    Energy Technology Data Exchange (ETDEWEB)

    Dahing, Lahasen Normanshah [School of Applied Physics, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor, Malaysia and Malaysian Nuclear Agency (Nuklear Malaysia), Bangi 43000, Kajang (Malaysia); Yahya, Redzuan [School of Applied Physics, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor (Malaysia); Yahya, Roslan; Hassan, Hearie [Malaysian Nuclear Agency (Nuklear Malaysia), Bangi 43000, Kajang (Malaysia)

    2014-09-03

    In this study, principle of prompt gamma neutron activation analysis has been used as a technique to determine the elements in the sample. The system consists of collimated isotopic neutron source, Cf-252 with HPGe detector and Multichannel Analysis (MCA). Concrete with size of 10×10×10 cm{sup 3} and 15×15×15 cm{sup 3} were analysed as sample. When neutrons enter and interact with elements in the concrete, the neutron capture reaction will occur and produce characteristic prompt gamma ray of the elements. The preliminary result of this study demonstrate the major element in the concrete was determined such as Si, Mg, Ca, Al, Fe and H as well as others element, such as Cl by analysis the gamma ray lines respectively. The results obtained were compared with NAA and XRF techniques as a part of reference and validation. The potential and the capability of neutron induced prompt gamma as tool for multi elemental analysis qualitatively to identify the elements present in the concrete sample discussed.

  10. Miniature Neutron-Alpha Activation Spectrometer

    Science.gov (United States)

    Rhodes, E.; Goldsten, J.

    2001-01-01

    We are developing a miniature neutron-alpha activation spectrometer for in situ analysis of samples including rocks, fines, ices, and drill cores, suitable for a lander or Rover platform, that would meet the severe mass, power, and environmental constraints of missions to the outer planets. In the neutron-activation mode, a gamma-ray spectrometer will first perform a penetrating scan of soil, ice, and loose material underfoot (depths to 10 cm or more) to identify appropriate samples. Chosen samples will be analyzed in bulk in neutron-activation mode, and then the sample surfaces will be analyzed in alpha-activation mode using Rutherford backscatter and x-ray spectrometers. The instrument will provide sample composition over a wide range of elements, including rock-forming elements (such as Na, Mg, Si, Fe, and Ca), rare earths (Sm and Eu for example), radioactive elements (K, Th, and U), and light elements present in water, ices, and biological materials (mainly H, C, O, and N). The instrument is expected to have a mass of about l kg and to require less than 1 W power. Additional information is contained in the original extended abstract.

  11. Neutron activation analysis in Romania

    International Nuclear Information System (INIS)

    Apostolescu, St.

    1985-01-01

    The following basic nuclear facilities are used for neutron activation analysis: a 2000 KW VVR-S Nuclear Reactor, a U-200 Cyclotron, a 30 MeV Betatron, several 14 MeV neutron generators and a king size High Voltage tandem Van de'Graaff accelerator. The main domains of application of the thermal neutron activation analysis are: geology and mining, processing of materials, environment and biology, achaeology. Epithermal neutron activation analysis has been used for determination of uranium and thorium in ores with high Th/U ratios or high rare earth contents. One low energy accelerator, used as 14.1 Mev neutron source, is provided with special equipmen for oxigen and low mass elements determination. An useful alternating way to support fast neutron activation analysis is an accurate theoretical description of the fast neutron induced reactions based on the statistical model (Hauser-Feubach STAPRE code) and the preequilibrium decay geometry dependent model. A gravitational sample changer has been installed at the end of a beam line of the Cyclotron, which enables to perform charged particles activation analysis for protein determination in grains

  12. Miniature neutron-alpha activation spectrometer

    International Nuclear Information System (INIS)

    Rhodes, Edgar; Goldsten, John; Holloway, James Paul; He, Zhong

    2002-01-01

    We are developing a miniature neutron-alpha activation spectrometer for in-situ analysis of chem-bio samples, including rocks, fines, ices, and drill cores, suitable for a lander or Rover platform for Mars or outer-planet missions. In the neutron-activation mode, penetrating analysis will be performed of the whole sample using a γ spectrometer and in the α-activation mode, the sample surface will be analyzed using Rutherford-backscatter and x-ray spectrometers. Novel in our approach is the development of a switchable radioactive neutron source and a small high-resolution γ detector. The detectors and electronics will benefit from remote unattended operation capabilities resulting from our NEAR XGRS heritage and recent development of a Ge γ detector for MESSENGER. Much of the technology used in this instrument can be adapted to portable or unattended terrestrial applications for detection of explosives, chemical toxins, nuclear weapons, and contraband

  13. Determination of uranium and thorium by neutron activation analysis applied to fossil samples dating

    International Nuclear Information System (INIS)

    Ticianelli, Regina B.; Figueiredo, Ana Maria Graciano; Zahn, Guilherme S.; Kinoshita, Angela; Baffa, Oswaldo

    2011-01-01

    Electron Spin Resonance (ESR) dating is based on the fact that ionizing radiation can create stable free radicals in insulating materials, like tooth enamel and bones. The concentration of these radicals - determined by ESR - is a function of the dose deposed in the sample along the years. The accumulated dose of radiation, called Archaeological Dose, is produced by the exposition to environmental radiation provided by U, Th, K and cosmic rays. If the environmental dose rate in the site where the fossil sample is found is known, it is possible to convert this dose into the age of the sample. The annual dose rate coming from the radioactive elements present in the soil and in the sample itself can be calculated by determining the U, Th and K concentration. Therefore, the determination of the dose rate depends on the concentration of these main radioactive elements. Neutron Activation Analysis has the sensitivity and the accuracy necessary to determine U, Th and K with this objective. Depending on the composition of the sample, the determination of U and Th can be improved irradiating the sample inside a Cd capsule, reducing the thermal neutron incidence on the sample and, therefore, diminishing the activation of possible interfering nuclides. In this study the optimal irradiation and counting conditions were established for U and Th determination in fossil teeth and soil. (author)

  14. Neutron Activation analysis of waste water

    International Nuclear Information System (INIS)

    Hernandez H, V.

    1997-01-01

    An instrumental neutron activation analysis for the simultaneous determination of chlorine, bromine, sodium, manganese, cobalt, copper, chromium, zinc, nickel, antimony and iron in waste water is described. They were determined in waste water samples under normal conditions by non-destructive neutron activation simultaneously using a suitable monostandard method. Standardized water samples were used and irradiated in polyethylene ampoules at a neutron flux of 10 13 cm -2 s -1 for periods of 1 minute, 1 and 10 hours. A Ge hyperpure detector was used for your activity determination, with count times of 60, 180, 300 and 600 seconds. The obtained results show than the method can be utilized for the determination of this elements without realize anything previous treatment of the samples. (Author)

  15. Computer-automated neutron activation analysis system

    International Nuclear Information System (INIS)

    Minor, M.M.; Garcia, S.R.

    1983-01-01

    An automated delayed neutron counting and instrumental neutron activation analysis system has been developed at Los Alamos National Laboratory's Omega West Reactor (OWR) to analyze samples for uranium and 31 additional elements with a maximum throughput of 400 samples per day. 5 references

  16. Analysis of coal by neutron activation

    International Nuclear Information System (INIS)

    Burtner, D.R.

    1983-01-01

    The development of a thermal-neutron activation analysis procedure for determining elemental concentrations in whole coal samples, and the goal of combining this technique with other nuclear methods for determining a total mass balance in these and similar complex materials, is described. Problems of applying a fast-neutron activation analysis method for nitrogen are discussed, as well as an efficient procedure for drying and packaging coal samples. A thermal-neutron activation analysis (TNAA) procedure was developed for determining up to 27 elements in coal samples from the US, China, Nigeria, and Brazil. The comparator form of TNAA was applied, using a unique multielement standard, which contained 48 elements. The difference in net photopeak counts between sample and standard, due to γ-ray attenuation, was reduced by preparing this standard in an organic matrix, which simulates the composition and physical structure of the coal material. The simultaneous irradiation of several aliquots of this standard enabled high precision and accuracy to be attained. An accurate value for oxygen, determined by fast-neutron activation analysis, is used to correct for this effect in the nitrogen determination method

  17. Neutron activation analysis of chemical impurities in manipulated samples of omeprazole

    International Nuclear Information System (INIS)

    Sepe, Fernanda Peixoto; Leal, Alexandre Soares; Gomes, Tatiana Cristina Bomfim; Menezes, Maria Angela de Barros Correia; Silva, Maria Aparecida

    2011-01-01

    In this work, samples of Omeprazole (C 17 H 19 N 3 O 3 S), a largely used drug in the treatment of dyspepsia and peptic ulcer, were acquired from five different pharmacies of manipulation - or retail pharmacies which prepare personalized drugs under medical recommendation - in Belo Horizonte/Brazil and investigated using the k 0 - Neutron Activation Analysis (NAA). The preliminary results showed the presence of elements not foreseen in the original formula. It confirms the potential risk offered by medicines without suitable inspection. (author)

  18. Improved mesh based photon sampling techniques for neutron activation analysis

    International Nuclear Information System (INIS)

    Relson, E.; Wilson, P. P. H.; Biondo, E. D.

    2013-01-01

    The design of fusion power systems requires analysis of neutron activation of large, complex volumes, and the resulting particles emitted from these volumes. Structured mesh-based discretization of these problems allows for improved modeling in these activation analysis problems. Finer discretization of these problems results in large computational costs, which drives the investigation of more efficient methods. Within an ad hoc subroutine of the Monte Carlo transport code MCNP, we implement sampling of voxels and photon energies for volumetric sources using the alias method. The alias method enables efficient sampling of a discrete probability distribution, and operates in 0(1) time, whereas the simpler direct discrete method requires 0(log(n)) time. By using the alias method, voxel sampling becomes a viable alternative to sampling space with the 0(1) approach of uniformly sampling the problem volume. Additionally, with voxel sampling it is straightforward to introduce biasing of volumetric sources, and we implement this biasing of voxels as an additional variance reduction technique that can be applied. We verify our implementation and compare the alias method, with and without biasing, to direct discrete sampling of voxels, and to uniform sampling. We study the behavior of source biasing in a second set of tests and find trends between improvements and source shape, material, and material density. Overall, however, the magnitude of improvements from source biasing appears to be limited. Future work will benefit from the implementation of efficient voxel sampling - particularly with conformal unstructured meshes where the uniform sampling approach cannot be applied. (authors)

  19. Neutron activation analysis of geological samples for gold and accessory elements power reactor

    International Nuclear Information System (INIS)

    Burmistrenko, Yu.N.; Medvedev, A.A.; Kovalenko, V.V.; Markov, A.V.

    1986-01-01

    Possibility of using a power reactor for neutron activation analysis to detect gold and accompanying elements in geological samples of a region was investigated. Specimens (gold-containing samples and standards) were irradiated in a spare channel for ionization chambers located outside the core in graphite reflector. Spectrometry was conducted with the help of a semiconducting detector with LP 4900 multichannel analizer. Sensitivity threshold for gold was (1-3)10 -6 % - (1-2)10 -5 %. It is shown that this method can be used not only for gold detection but for high-sensitive multielement analysis of geological samples

  20. Determination of Magnesium in Needle Biopsy Samples of Muscle Tissue by Means of Neutron Activation Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Brune, D; Sjoeberg, H E

    1964-07-15

    Magnesium has been determined by means of neutron-activation analysis in needle biopsy samples of the order of magnitude 1 mg dry weight. The procedure applied was to extract the Mg-27 activity from irradiated muscle tissue with concentrated hydrochloric acid followed by a fast hydroxide precipitation and gamma-spectrometric measurements. The Mg activity was recovered in the muscle tissue samples to (97 {+-} 2) per cent. The sensitivity for the magnesium determination is estimated as 0.3 {mu}g.

  1. Neutron activation analysis of chemical impurities in manipulated samples of omeprazole

    Energy Technology Data Exchange (ETDEWEB)

    Sepe, Fernanda Peixoto; Leal, Alexandre Soares; Gomes, Tatiana Cristina Bomfim; Menezes, Maria Angela de Barros Correia; Silva, Maria Aparecida, E-mail: asleal@cdtn.br [Nuclear Technology Development Centre/Brazilian Commission for Nuclear Energy (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2011-07-01

    In this work, samples of Omeprazole (C{sub 17}H{sub 19}N{sub 3}O{sub 3}S), a largely used drug in the treatment of dyspepsia and peptic ulcer, were acquired from five different pharmacies of manipulation - or retail pharmacies which prepare personalized drugs under medical recommendation - in Belo Horizonte/Brazil and investigated using the k{sub 0} - Neutron Activation Analysis (NAA). The preliminary results showed the presence of elements not foreseen in the original formula. It confirms the potential risk offered by medicines without suitable inspection. (author)

  2. Dynamically Polarized Sample for Neutron Scattering At the Spallation Neutron Source

    International Nuclear Information System (INIS)

    Pierce, Josh; Zhao, J. K.; Crabb, Don

    2009-01-01

    The recently constructed Spallation Neutron Source at the Oak Ridge National Laboratory is quickly becoming the world's leader in neutron scattering sciences. In addition to the world's most intense pulsed neutron source, we are continuously constructing state of the art neutron scattering instruments as well as sample environments to address today and tomorrow's challenges in materials research. The Dynamically Polarized Sample project at the SNS is aimed at taking maximum advantage of polarized neutron scattering from polarized samples, especially biological samples that are abundant in hydrogen. Polarized neutron scattering will allow us drastically increase the signal to noise ratio in experiments such as neutron protein crystallography. The DPS project is near completion and all key components have been tested. Here we report the current status of the project.

  3. Forensic neutron activation analysis

    International Nuclear Information System (INIS)

    Kishi, T.

    1987-01-01

    The progress of forensic neutron activation analysis (FNAA) in Japan is described. FNAA began in 1965 and during the past 20 years many cases have been handled; these include determination of toxic materials, comparison examination of physical evidences (e.g., paints, metal fragments, plastics and inks) and drug sample differentiation. Neutron activation analysis is applied routinely to the scientific criminal investigation as one of multielement analytical techniques. This paper also discusses these routine works. (author) 14 refs

  4. Sample registration software for process automation in the Neutron Activation Analysis (NAA) Facility in Malaysia nuclear agency

    Energy Technology Data Exchange (ETDEWEB)

    Rahman, Nur Aira Abd, E-mail: nur-aira@nuclearmalaysia.gov.my; Yussup, Nolida; Ibrahim, Maslina Bt. Mohd; Mokhtar, Mukhlis B.; Soh Shaari, Syirrazie Bin Che; Azman, Azraf B. [Technical Support Division, Malaysian Nuclear Agency, 43000, Kajang, Selangor (Malaysia); Salim, Nazaratul Ashifa Bt. Abdullah [Division of Waste and Environmental Technology, Malaysian Nuclear Agency, 43000, Kajang, Selangor (Malaysia); Ismail, Nadiah Binti [Fakulti Kejuruteraan Elektrik, UiTM Pulau Pinang, 13500 Permatang Pauh, Pulau Pinang (Malaysia)

    2015-04-29

    Neutron Activation Analysis (NAA) had been established in Nuclear Malaysia since 1980s. Most of the procedures established were done manually including sample registration. The samples were recorded manually in a logbook and given ID number. Then all samples, standards, SRM and blank were recorded on the irradiation vial and several forms prior to irradiation. These manual procedures carried out by the NAA laboratory personnel were time consuming and not efficient. Sample registration software is developed as part of IAEA/CRP project on ‘Development of Process Automation in the Neutron Activation Analysis (NAA) Facility in Malaysia Nuclear Agency (RC17399)’. The objective of the project is to create a pc-based data entry software during sample preparation stage. This is an effective method to replace redundant manual data entries that needs to be completed by laboratory personnel. The software developed will automatically generate sample code for each sample in one batch, create printable registration forms for administration purpose, and store selected parameters that will be passed to sample analysis program. The software is developed by using National Instruments Labview 8.6.

  5. Sample registration software for process automation in the Neutron Activation Analysis (NAA) Facility in Malaysia nuclear agency

    Science.gov (United States)

    Rahman, Nur Aira Abd; Yussup, Nolida; Salim, Nazaratul Ashifa Bt. Abdullah; Ibrahim, Maslina Bt. Mohd; Mokhtar, Mukhlis B.; Soh@Shaari, Syirrazie Bin Che; Azman, Azraf B.; Ismail, Nadiah Binti

    2015-04-01

    Neutron Activation Analysis (NAA) had been established in Nuclear Malaysia since 1980s. Most of the procedures established were done manually including sample registration. The samples were recorded manually in a logbook and given ID number. Then all samples, standards, SRM and blank were recorded on the irradiation vial and several forms prior to irradiation. These manual procedures carried out by the NAA laboratory personnel were time consuming and not efficient. Sample registration software is developed as part of IAEA/CRP project on `Development of Process Automation in the Neutron Activation Analysis (NAA) Facility in Malaysia Nuclear Agency (RC17399)'. The objective of the project is to create a pc-based data entry software during sample preparation stage. This is an effective method to replace redundant manual data entries that needs to be completed by laboratory personnel. The software developed will automatically generate sample code for each sample in one batch, create printable registration forms for administration purpose, and store selected parameters that will be passed to sample analysis program. The software is developed by using National Instruments Labview 8.6.

  6. Activation measurements for thermal neutrons. Part J. Evaluation of thermal neutron transmission factors

    International Nuclear Information System (INIS)

    Egbert, Stephen D.

    2005-01-01

    In order to relate thermal neutron activation measurements in samples to the calculated free-in-air thermal neutron activation levels given in Chapter 3, use is made of sample transmission factors. Transmission factors account for the modification of the fluence and activation at each sample's in situ location. For the purposes of this discussion, the transmission factor (TF) is defined as the ratio of the in situ sample activation divided by the free-in-air (FIA) activation at a height of 1 m above ground at the same ground range. The procedures for calculation of TF's and example results are presented in this section. (author)

  7. Determination of phosphorus in wheat grass samples by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Kulkarni, S.D.; Rajurkar, N.S.; Acharya, R.; Nair, A.G.C.; Reddy, A.V.R.

    2005-01-01

    An instrumental neutron activation analysis (INAA) method using β-counting was used to determine phosphorus in wheat grass; grown in three different conditions. The phosphorus concentration was found to be in the range of 950-23000 mg/g in the samples grown in different conditions. The accuracy of the method was evaluated by determining phosphorus in three reference materials and the % deviations were within 10%. Reliability of the method was checked by following the half-life of the 32 P. (author)

  8. Determination of phosphorus using derivative neutron activation

    International Nuclear Information System (INIS)

    Scindia, Y.M.; Nair, A.G.C.; Reddy, A.V.R.; Manohar, S.B.

    2002-01-01

    For the determination of phosphorus in different matrices, the derivative neutron activation analysis is especially applicable to aqueous samples, since the conventional neutron activation analysis is not useful for the determination of phosphorus. Phosphorus when reacted with ammonium molybdate 4 hydrate and ammonium metavanadate forms molybdo vanado phosphoric acid. This complex is preconcentrated by extracting into methyl isobutyl ketone. The organic phase containing the molybdo vanado phosphoric acid is neutron activated and the phosphorus is determined through the activation product of 52 V. Preparation of this complex, its stoichiometry, application to trace level determination of phosphorus and improved detection limit are discussed. This method was applied for the analysis of industrial effluent samples. (author)

  9. On multielement analysis of biological samples with the aid of neutron activation

    International Nuclear Information System (INIS)

    Iyengar, G.V.

    1980-01-01

    A main objective of this study was elucidation of problems of sampling and sample preparation methods for multielement analysis of environmental and biological specimens. Another was assessment of the potentials of multielement neutron activation analysis (NAA) in environmental and biological research. In an attempt to explain the great differences in the elemental concentration ranges between biopsy and autopsy samples as reported in the literature, it was shown that post mortem changes induce great variations in the apparent elemental composition of autopsy specimens resulting in serious systematic errors. Applications of NAA to analysis of tissues of experimental animals, human tissues in health and disease, and environmental samples are illustrated with several examples. The suitability of NAA for routine analysis of elements such as Cr, Mo and Se, which are difficult to determine by other methods has been specially discussed. (author)

  10. The development of an automatic sample-changer and control instrumentation for isotope-source neutron-activation analysis

    International Nuclear Information System (INIS)

    Andeweg, A.H.; Watterson, J.I.W.

    1983-01-01

    An automatic sample-changer was developed at the Council for Mineral Technology for use in isotope-source neutron-activation analysis. Tests show that the sample-changer can transfer a sample of up to 3 kg in mass over a distance of 3 m within 5 s. In addition, instrumentation in the form of a three-stage sequential timer was developed to control the sequence of irradiation transfer and analysis

  11. Activation analysis by filtered neutrons. Preliminary investigation

    International Nuclear Information System (INIS)

    Skarnemark, G.; Rodinson, T.; Skaalberg, M.; Tokay, R.K.

    1986-01-01

    In order to investigate if measuring sensibility and precision by epithermal neutron activation analysis may be improved, different types of geological and biologic test samples were radiated. The test samples were enclosed in an extra filter of tungsten or sodium in order to reduce the flux of those neutrons that otherwise would induce interfering activity in the sample. The geological test samples consist of granites containing lanthanides which had been crushed in tung- sten carbide grinder. Normally such test samples show a interferins 1 87W-activity. By use of a tungsten filter the activity was reduced by up to 60%, which resulted in a considerable improvement of sensibility and precision of the measurement. The biologic test samples consisted of evaporated urine from patients treated with the cell poison cis-platinol. A reliable method to measure the platinum content has not existed so far. This method, however, enables platinum contents as low as about 0.1 ppm to be determined which is quite adequate. To sum up this preliminary study has demonstrated that activation analysis using filtered neutrons, correctly applied, is a satisfactory method of reducing interferences without complicated and time-consuming chemical separation procedures. (O.S.)

  12. Iron Quadrangle, Brazil. Elemental concentration determined by k0-instrumental neutron activation analysis. Part 1. Soil 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 Iron Quadrangle, Minas Gerais, Brazil, is rich in mineral occurrences and is considered one of the richest mineral-bearing regions in the world. Most investigations in this region have dealt with the determination of arsenic and mercury but so far few studies have been carried out aiming at determining other important elements. Having in mind the potential risk caused by mineral activities, this study was developed in order to assess the potential influence of the soil on foodstuffs. The soil samples were collected from three sites inside and outside the Iron Quadrangle. The samples were analyzed at the Laboratory for Neutron Activation Analysis, CDTN/CNEN by the k 0 -instrumental neutron activation analysis. This paper reports the elemental concentration determined in soil and emphasises the elements cited in the Brazilian environmental legislation for soil. This work also confirms the high elemental concentration of several minerals, however, it is difficult to distinguish the contamination from anthropogenic activities from the natural occurrence. (author)

  13. A study on aluminum determination in environmental samples by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Noyori, Amanda

    2017-01-01

    Aluminum determinations are of great interest since this element is toxic to humans and it is widely distributed in the environment. Besides, the determinations of this element by conventional analytical methods present difficulties due to sample contamination during the analyses. Neutron activation analysis (NAA) for Al determination presents advantages of fast analyses and of high sensitivity. However, NAA of Al does present problems of P and Si nuclear reaction interferences. Aluminum is determined by measuring 28 Al, formed in the reaction 27 Al (n, γ) 28 Al, the same radioisotope formed in reactions 31 P (n, α) 28 Al and 28 Si (n, p) 28 Al. The purpose of this study was to determine Al in environmental samples by NAA correcting these interferences using correction factors, and determining P and Si concentrations in the samples. In this study, certified reference materials and biomonitor samples (tree barks and lichen) were analyzed. Experimental procedure consisted of irradiating an aliquot of the sample at the IEA-R1 nuclear research reactor together with Al standard, followed by gamma ray spectrometry. Phosphorus was determined by measuring beta radiation of 32 P using a Geiger-Müller counter. Silicon was determined by epithermal neutron activation analysis and measuring 29 Al formed in the reaction 29 Si (n, p) 29 Al. Results obtained in the determination of Al, P and Si in the certified reference materials showed good precision and accuracy with |Z-score| ≤ 2. Aluminum results in the biomonitor samples varied from to 253 to 15783 μg g -1 . In the case of P its concentrations varied from 283 to 1946 μg g -1 . Silicon determinations in biomonitors varied from 0.11 to 7.8 %. The interference contribution rates in the analyses of the biomonitor samples were of the order of 2.0 % and this contribution depends on the relation between concentrations of interfering elements and of Al in the sample. Detection limit values of Al in the biomonitor analyses

  14. Development and installation of an automatic sample changer for neutron activation analysis

    International Nuclear Information System (INIS)

    Domienikan, Claudio; Lapolli, Andre L.; Schoueri, Roberto M.; Moreira, Edson G.; Vasconcellos, Marina B.A.

    2013-01-01

    A Programmable and Automatic Sample Changer was built and installed at the Neutron Activation Analysis Laboratory of the Nuclear and Energy Research Institute - IPEN-CNEN/SP, Brazil. This Automatic Sample Changer allows the fully automated measurement of up to 25 samples in one run. Basically it consists of an electronic circuit and C++ program that controls the positioning of a sample holder in two axes of motion (X and Y). Each sample is transported and positioned, one by one, inside the shielding coupled to a high-purity germanium (HPGe) radiation detector. A Canberra DSA-1000 Multichannel Analyzer coupled to the Genie 2000 software performs the data acquisition for analysis of the samples. When the counting is finished the results are saved in a hard disk of a PC computer. The sample is brought back by the sample holder to its initial position, and the next sample is carried to the shielding. The Sample Changer was designed and constructed at IPEN-CNEN/SP by employing national components and expertise. (author)

  15. Prompt gamma neutron activation analysis

    International Nuclear Information System (INIS)

    Goswami, A.

    2003-01-01

    Prompt gamma neutron activation analysis (PGNAA) is a technique for the analysis of elements present in solid, liquid and gaseous samples by measuring the capture gamma rays emitted from the sample during neutron irradiation. The technique is complementary to conventional neutron activation analysis (NAA) as it can be used in number of cases where NAA fails. Though the technique was first used in sixties, the advantage of the technique was first highlighted by Lindstrom and Anderson. PGNAA is increasingly being used as a rapid, instrumental, nondestructive and multielement analysis technique. A monograph and several excellent reviews on this topic have appeared recently. In this review, an attempt has been made to bring out the essential aspects of the technique, experimental arrangement and instrumentation involved, and areas of application. Some of the results will also be presented

  16. SNS Sample Activation Calculator Flux Recommendations and Validation

    Energy Technology Data Exchange (ETDEWEB)

    McClanahan, Tucker C. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Spallation Neutron Source (SNS); Gallmeier, Franz X. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Spallation Neutron Source (SNS); Iverson, Erik B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Spallation Neutron Source (SNS); Lu, Wei [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Spallation Neutron Source (SNS)

    2015-02-01

    The Spallation Neutron Source (SNS) at Oak Ridge National Laboratory (ORNL) uses the Sample Activation Calculator (SAC) to calculate the activation of a sample after the sample has been exposed to the neutron beam in one of the SNS beamlines. The SAC webpage takes user inputs (choice of beamline, the mass, composition and area of the sample, irradiation time, decay time, etc.) and calculates the activation for the sample. In recent years, the SAC has been incorporated into the user proposal and sample handling process, and instrument teams and users have noticed discrepancies in the predicted activation of their samples. The Neutronics Analysis Team validated SAC by performing measurements on select beamlines and confirmed the discrepancies seen by the instrument teams and users. The conclusions were that the discrepancies were a result of a combination of faulty neutron flux spectra for the instruments, improper inputs supplied by SAC (1.12), and a mishandling of cross section data in the Sample Activation Program for Easy Use (SAPEU) (1.1.2). This report focuses on the conclusion that the SAPEU (1.1.2) beamline neutron flux spectra have errors and are a significant contributor to the activation discrepancies. The results of the analysis of the SAPEU (1.1.2) flux spectra for all beamlines will be discussed in detail. The recommendations for the implementation of improved neutron flux spectra in SAPEU (1.1.3) are also discussed.

  17. Sample dependent response of a LaCl{sub 3}:Ce detector in prompt gamma neutron activation analysis of bulk hydrocarbon samples

    Energy Technology Data Exchange (ETDEWEB)

    Naqvi, A.A., E-mail: aanaqvi@kfupm.edu.sa [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran (Saudi Arabia); Al-Matouq, Faris A.; Khiari, F.Z. [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran (Saudi Arabia); Isab, A.A. [Department of Chemistry, King Fahd University of Petroleum and Minerals, Dhahran (Saudi Arabia); Khateeb-ur-Rehman,; Raashid, M. [Department of Physics, King Fahd University of Petroleum and Minerals, Dhahran (Saudi Arabia)

    2013-08-11

    The response of a LaCl{sub 3}:Ce detector has been found to depend upon the hydrogen content of bulk samples in prompt gamma analysis using 14 MeV neutron inelastic scattering. The moderation of 14 MeV neutrons from hydrogen in the bulk sample produces thermal neutrons around the sample which ultimately excite chlorine capture gamma rays in the LaCl{sub 3}:Ce detector material. Interference of 6.11 MeV chlorine gamma rays from the detector itself with 6.13 MeV oxygen gamma rays from the bulk samples makes the intensity of the 6.13 MeV oxygen gamma ray peak relatively insensitive to variations in oxygen concentration. The strong dependence of the 1.95 MeV doublet chlorine gamma ray yield on hydrogen content of the bulk samples confirms fast neutron moderation from hydrogen in the bulk samples as a major source of production of thermal neutrons and chlorine gamma rays in the LaCl{sub 3}:Ce detector material. Despite their poor oxygen detection capabilities, these detectors have nonetheless excellent detection capabilities for hydrogen and carbon in benzene, butyl alcohol, propanol, propanic acid, and formic acid bulk samples using 14 MeV neutron inelastic scattering.

  18. Applications of neutrons for laboratory and industrial activation analysis problems

    International Nuclear Information System (INIS)

    Szabo, Elek; Bakos, Laszlo

    1986-01-01

    This chapter presents some particular applications and case studies of neutrons in activation analysis for research and industrial development purposes. The reactor neutrons have been applied in Hungarian laboratories for semiconductor research, for analysis of geological (lunar) samples, and for a special comparator measurement of samples. Some industrial applications of neutron generator and sealed sources for analytical problems are presented. Finally, prompt neutron activation analysis is outlined briefly. (R.P.)

  19. Determination of phosphorus and calcium in biological samples by activation with 14 MeV neutrons

    International Nuclear Information System (INIS)

    Berretta, Jose Roberto

    1995-01-01

    Analytical methods for phosphorus and calcium in biological samples by means of activation with 14 MeV neutrons, using the Van de Graaff accelerator from the Instituto de Pesquisas Energeticas e Nucleares, SP, Brazil are developed. For phosphorus analysis, powder samples were pressed into pellets, weighed and transferred to polyethylene plastic envelopes. The pellets with cadmium shielding were irradiated under a fast neutron flux for 5 to 10 minutes, and further counted in a HPGe detector for 5 minutes. Calcium analysis was performed by cyclic irradiation. Samples were irradiated for 10 minutes. After a decay time of 2 minutes, gamma counting was performed for 10 minutes. After a decay time of 2 minutes, a new irradiation ws made. The irradiation cycle was repeated 5 times and the counting spectrum obtained in each cycle was accumulated in the multi channel analyser. The variation of the neutron flux was followed by using a BF 3 detector calibrated with and aluminium monitor. By means of the gamma spectrum and the neutron counting of the BF 3 detector it was possible to estimate phosphorus and calcium concentrations in the sample analyzed. The methods were checked in the reference samples from the International Atomic Energy Agency and in commercial samples of powder milk, fertilizer and animal bone. Phosphorus contents in bone (A3/74) and milk (A-11) reference materials were (15.6 +- 1.8%) and (0.9 +- 0.1)%, respectively. These values are in good agreement to the certified values (15.5 +- 0.5)% and (0.910 +- 0.102)%, respectively. Calcium analysis carried out in bone (A3/74) presented a value of (31.8+-4.1)% and the certified value was of (31.3 +- 0.3)%. Detection limits for phosphorus and calcium were determined in different analyzed samples. The agreement of the results obtained with the certified values confirmed the suitability of the methods for phosphorus and calcium analysis. The methods are fast and laborious chemical procedures are not required. (author)

  20. Neutron activation analysis: principle and methods

    International Nuclear Information System (INIS)

    Reddy, A.V.R.; Acharya, R.

    2006-01-01

    Neutron activation analysis (NAA) is a powerful isotope specific nuclear analytical technique for simultaneous determination of elemental composition of major, minor and trace elements in diverse matrices. The technique is capable of yielding high analytical sensitivity and low detection limits (ppm to ppb). Due to high penetration power of neutrons and gamma rays, NAA experiences negligible matrix effects in the samples of different origins. Depending on the sample matrix and element of interest NAA technique is used non-destructively, known as instrumental neutron activation analysis (INAA), or through chemical NAA methods. The present article describes principle of NAA, different methods and gives a overview some applications in the fields like environment, biology, geology, material sciences, nuclear technology and forensic sciences. (author)

  1. Application of the neutron activation analysis method for determing trace elements in Brazilian food sample

    International Nuclear Information System (INIS)

    Maihara, V.A.; Vasconcellos, M.B.A.

    1988-01-01

    Recently there has been an increase of consciousness about the importance of trace elements in human health and disease as well as rising concern about food contamination. The development of sensitive, accurate and price methods is one of the most important of the knowledge of trace elements contents in foods and in biological samples. Neutron activation analysis is one of the most suitable tecniques because a great number of elements can be determined in concentrations in the range of μg/g to ng/g. The present work is a part of an AIEA Co-ordinated Research Programme on the applications of nuclear techniques for toxic elements in foodstuffs. Neutron activation analysis is applied to analysis of bread, milk powder and rice that are considered essential foods in the Brazilian diet. Some aspects of the activation analysis of biological matrices are discussed. (author) [pt

  2. High-capacity neutron activation analysis facility

    International Nuclear Information System (INIS)

    Hochel, R.C.

    1979-01-01

    A high-capacity neutron activation analysis facility, the Reactor Activation Facility, was designed and built and has been in operation for about a year at one of the Savannah River Plant's production reactors. The facility determines uranium and about 19 other trace elements in hydrogeochemical samples collected in the National Uranium Resource Evaluation program. The facility has a demonstrated average analysis rate of over 10,000 samples per month, and a peak rate of over 16,000 samples per month. Uranium is determined by cyclic activation and delayed neutron counting of the U-235 fission products; other elements are determined from gamma-ray spectra recorded in subsequent irradiation, decay, and counting steps. The method relies on the absolute activation technique and is highly automated for round-the-clock unattended operation

  3. Analysis of medicinal plants and soil sample from Haridwar region by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Maharia, R.S.; Dutta, R.K.; Acharya, R.; Reddy, A.V.R.

    2009-01-01

    Samples of leaves and stems of four medicinal plants namely Kalmegh, Amaltas, Moalshri, and Arusa were analysed by Instrumental Neutron Activation Analysis. Soil from same location was analyzed. Though concentrations of many elements were determined in the plant samples, results of selected elements namely Na, K, Mn, Fe, Co, Cr, Zn and As are discussed in this paper. The results show that all medicinal plants analyzed have lower elemental contents except Zn compared to the soil. (author)

  4. Determination of organic fluorine in aqueous samples with neutron activation analysis in comparison with the DIN method

    Energy Technology Data Exchange (ETDEWEB)

    Rollinger, D. [Institut fuer Kernchemie, Universitaet Mainz, Fritz-Strassmann-Weg 2, D-55099 Mainz (Germany); Kratz, K.L. [Institut fuer Kernchemie, Universitaet Mainz, Fritz-Strassmann-Weg 2, D-55099 Mainz (Germany)

    1996-04-01

    Neutron activation analysis (NAA) has been used as detection technique for adsorbable organic fluorine in aqueous samples. The results have been compared with the standardized DIN method which uses a fluoride-ion-selective electrode (ISE). (orig.). With 3 tabs.

  5. Activation Measurements for Thermal Neutrons, Part D. U.S. Measurements of 36Cl in Mineral Samples from Hiroshima and Nagasaki

    International Nuclear Information System (INIS)

    Tore Straume; Alfredo A, Marchetti; Stephen D, Egbert; James A, Roberts; Ping Men; Shoichiro Fujita; Kiyoshi Shizuma; Masaharu Hoshi; G, Rugel; W, Ruhm; G, Korschinek; J. E. McAninch; K. L. Carroll; T. Faestermann; K. Knie; R. E. Martinelli; A. Wallner; C. Wallner

    2005-01-01

    The present paper presents the 36 Cl measurement effort in the US. A large number of 36 Cl measurements have been made in both granite and concrete samples obtained from various locations and distances in Hiroshima and Nagasaki. These measurements employed accelerator mass spectrometry (AMS) to quantify the number of atoms of 36 Cl per atom of total Cl in the sample. Results from these measurements are presented here and discussed in the context of the DS02 dosimetry reevaluation effort for Hiroshima and Nagasaki atomic-bomb survivors. The production of 36 Cl by bomb neutrons in mineral samples from Hiroshima and Nagasaki was primarily via the reaction 35 Cl(n,γ) 36 Cl. This reaction has a substantial thermal neutron cross-section (43.6 b at 0.025 eV) and the product has a long half-life (301,000 y). hence, it is well suited for neutron-activation detection in Hiroshima and Nagasaki using AMS more than 50 years after the bombings. A less important reaction for bomb neutrons, 39 K(n,α) 36 Cl, typically produces less than 10% of the 36 Cl in mineral samples such as granite and concrete, which contain ∼ 2% potassium. In 1988, only a year after the publication of the DS86 final report (Roesch 1987), it was demonstrated experimentally that 36 Cl measured using AMS should be able to detect the thermal neutron fluences at the large distances most relevant to the A-bomb survivor dosimetry. Subsequent measurements in mineral samples from both Hiroshima and Nagasaki validated the experimental findings. The potential utility of 36 Cl as a thermal neutron detector in Hiroshima was first presented by Haberstock et al. who employed the Munich AMS facility to measure 36 Cl/Cl ratios in a gravestone from near the hypocenter. That work subsequently resulted in an expanded 36 Cl effort in Germany that paralleled the US work. More recently, there have also been 36 Cl measurements made by a Japanese group. The impetus for the extensive 36 Cl and other neutron activation

  6. Recent applications of neutron activation analysis at Lucas Heights

    International Nuclear Information System (INIS)

    Fardy, J.J.

    1978-01-01

    The use of neutron activation analysis to determine key elemental distribution patterns in samples from both the energy industry and health science field is summarised. Instrumental neutron activation analysis has successfully measured simultaneously more than twenty elements in a sample of brown coal from Victoria, black coal from New South Wales and samples from the product stream of ACIRL's batch autoclave, solvent-refined, coal hydrogenation process. Four gallstones removed from the same gallbladder have been examined instrumentally by neutron activation analysis. A total of sixteen trace elements were detected with concentrations in the range 0.8 ng g -1 for gold to 7,800 μg g -1 for calcium

  7. Neutron moderation in a bulk sample and its effects on PGNAA setup geometry

    International Nuclear Information System (INIS)

    Al-Jarallah, M.I.; Naqvi, A.A.; Fazal-ur-Rehman,; Maselehuddin, M.; Abu-Jarad, F.; Raashid, M.

    2003-01-01

    In a prompt gamma ray neutron activation analysis (PGNAA) setup, the neutron moderation in the bulk sample also plays a key role. This can even dominate the thermalization effects of the external moderator in some cases. In order to study the neutron moderation effect in the bulk sample, moderators with two different sizes of the sample were tested at the King Fahd University of Petroleum and Minerals (KFUPM) PGNAA facility. In these tests, the thermal neutron relative intensity and prompt gamma ray yield from the two moderators were measured using nuclear track detectors (NTDs) and NaI detector, respectively. As predicted by Monte Carlo simulations, the measured intensity of thermal neutron inside the large sample cavity due to the external moderator was smaller than that from the smaller sample cavity. Due to its larger size, additional thermalization of neutrons will take place in the larger sample. In spite of smaller thermal neutron yield from the external moderator at the large sample location, higher yield of the prompt gamma ray was observed as compared to that from the smaller sample. This confirms the significance of neutron moderation effects in the bulk sample and can thereby affect the PGNAA geometry size. This allows larger samples in conjunction with smaller moderators in the PGNAA setup

  8. Neutron moderation in a bulk sample and its effects on PGNAA setup geometry

    Energy Technology Data Exchange (ETDEWEB)

    Al-Jarallah, M.I. E-mail: mibrahim@kfupm.edu.sa; Naqvi, A.A.; Fazal-ur-Rehman,; Maselehuddin, M.; Abu-Jarad, F.; Raashid, M

    2003-06-01

    In a prompt gamma ray neutron activation analysis (PGNAA) setup, the neutron moderation in the bulk sample also plays a key role. This can even dominate the thermalization effects of the external moderator in some cases. In order to study the neutron moderation effect in the bulk sample, moderators with two different sizes of the sample were tested at the King Fahd University of Petroleum and Minerals (KFUPM) PGNAA facility. In these tests, the thermal neutron relative intensity and prompt gamma ray yield from the two moderators were measured using nuclear track detectors (NTDs) and NaI detector, respectively. As predicted by Monte Carlo simulations, the measured intensity of thermal neutron inside the large sample cavity due to the external moderator was smaller than that from the smaller sample cavity. Due to its larger size, additional thermalization of neutrons will take place in the larger sample. In spite of smaller thermal neutron yield from the external moderator at the large sample location, higher yield of the prompt gamma ray was observed as compared to that from the smaller sample. This confirms the significance of neutron moderation effects in the bulk sample and can thereby affect the PGNAA geometry size. This allows larger samples in conjunction with smaller moderators in the PGNAA setup.

  9. Application of the neutron activation analysis method to the multielemental determination of food samples

    International Nuclear Information System (INIS)

    Maihara, V.A.

    1985-01-01

    The thermal neutron activation analysis method was applied to the determination of elements present at low concentrations and trace levels in samples of bread and milk powder using non-destructive analyses were based on gamma ray spectrometric measurements of samples and standards irradiated for periods which varied from some minutes to eight hours in a thermal neutron flux of about 10 12 n cm -2 s -1 . The concentrations obtained for milk powder were compared with the data obtained by other autors from different contries. For the bread, that comparison was not possible, because data about trace analysis in bread samples were not found. Besides, the results obtained for the various brands of bread and milk by means of non destructive and destructive analyses were compared using Student's t criterion. Some basic considerations about 'Detection Limit' were done, mainly in relation to its application in the technique used in the present work. The detection and determination limits of the trace elements analysed by destructive and non destructive techniques in bread and milk powder samples were determined using the Currie and Girardi methods. The precision of the analyses and the results obtained for the detection limits of the analysed trace elements are discussed. (Author) [pt

  10. Determination of silver, gold, zinc and copper in mineral samples by various techniques of instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Rodriguez R, N. I.; Rios M, C.; Pinedo V, J. L.; Yoho, M.; Landsberger, S.

    2015-09-01

    Using the method of instrumental neutron activation analysis, mineral exploration samples were analyzed in order to determine the concentrations of silver, gold, zinc and copper; these minerals being the main products of benefit of Tizapa and Cozamin mines. Samples were subjected to various techniques, where the type of radiation and counting methods were chosen based on the specific isotopic characteristics of each element. For calibration and determination of concentrations the comparator method was used, certified standards were subjected to the same conditions of irradiation and measurement that the prospecting samples. The irradiations were performed at the research reactor TRIGA Mark II of the University of Texas at Austin. The silver concentrations were determined by Cyclical Epithermal Neutron Activation Analysis. This method in combination with the transfer pneumatic system allowed a good analytical precision and accuracy in prospecting for silver, from photo peak measurement 657.7 keV of short half-life radionuclide 110 Ag. For the determination of gold and zinc, Epithermal Neutron Activation Analysis was used, the photo peaks analyzed corresponded to the energies 411.8 keV of radionuclide 199 Au and 438.6 keV of metastable radionuclide 69m Zn. On the other hand, copper quantification was based on the photo peak analysis of 1039.2 keV produced by the short half-life radionuclide 66 Cu, by Thermal Neutron Activation Analysis. The photo peaks measurement corresponding to gold, zinc and copper was performed using a Compton suppression system, which allowed an improvement in the signal to noise relationship, so that better detection limits and low uncertainties associated with the results were obtained. Comparing elemental concentrations the highest values in silver, zinc and copper was for samples of mine Tizapa. Regarding gold values were found in the same range for both mines. To evaluate the precision and accuracy of the methods used, various geological

  11. APPLICATION OF NEUTRON ACTIVATION ANALYSIS IN CHARACTERIZATION OF ENVIRONMENTAL SRM SAMPLES

    Directory of Open Access Journals (Sweden)

    Diah Dwiana Lestiani

    2010-06-01

    Full Text Available Neutron activation analysis (NAA is a nuclear technique that is excellent, multi-elemental, sensitive and has limit detection up to nanogram level. The application of NAA in analysis of Standard Reference Material (SRM National Institute of Standard Technology (NIST 1633b Coal Fly Ash and SRM NIST 1646a Estuarine Sediment was carried out for NAA laboratory inter-comparison program. The samples were distributed by Technology Centre for Nuclear Industry Material, National Nuclear Energy Agency as a coordinator of the inter-comparison program. The samples were irradiated in rabbit facility of G.A. Siwabessy reactor with neutron flux ~ 1013 n.cm-2.s-1, and counted with HPGe spectrometry gamma detector. Several trace elements in these samples were detected. The concentration of Al, Mg, K, Na and Ti in SRM NIST 1633b were 15.11, 7.35, 2.09, 0.192 and 0.756% respectively and the concentration of As, Cr, Mn, Se, V, Sb, Co, Cs, La, Sc and Sm were 137.0, 195.6, 129.4, 9.61, 305.8, 5.45, 56.2, 11.18, 83.73, 41.1 and 19.13 mg/kg respectively. The analysis result in SRM NIST 1646a of the concentration of Al and Na were 2.15 and 0.70% and the concentration of As, Cr, Co, La and Sc were 5.75, 36.3, 4.58, 15.67 and 4.00 mg/kg respectively. These results analysis had relative bias and u-test ranged from 0.4-11.3% and 0.15-2.25. The accuracy and precision evaluation based on International Atomic Energy Agency (IAEA criteria was also applied. The result showed that NAA technique is applicable for the environmental samples analysis, and it also showed that the NAA laboratory in BATAN Bandung has a good performance.   Keywords: NAA, inter-comparison, estuarine sediment, coal fly ash, environmental samples

  12. Vanadium determination in pretoleum by neutron activation analysis

    International Nuclear Information System (INIS)

    Lopez, M.; Espinosa, R.

    1983-01-01

    The vanadium concentration in an Peruvian petroleum sample is determined by neutron activation analysis. The samples were irradiated for 20 minutes with a flux of thermal neutrons of 1.75 x 10 7 n/cm 2 -s in a subcritical assembly. The activity of the created samples decreases to half 15 minutes after the irradiation. The result is 28.3 +- 0.8 p.p.m. with a typical deviation of 2.8%. The detection limit of this method is 4 p.p.m

  13. Investigation of Hg volatile losses from samples and standards during neutron activation analysis

    International Nuclear Information System (INIS)

    Dubinskaya, N.; Dundua, V.; Chikhladze, N.

    1979-01-01

    The losses of Hg from phenol formaldehyde resin - bound standards and hair samples in neutron activation analysis in case of their irradiation in the water filled nuclear reactor channel is studied. The mean losses of Hg during 20-30 hrs irradiation at (2-3)x10 18 n/cm 2 are 15-20% with their stopping at double Al-covers. The mean losses of Hg from standards at 200, 250 and 300 deg C are 30, 61 and 86% respectively and do not occur at 150 deg C after their 5 hour heating. The losses of Hg from hair samples packed in polyethylene tubes through the package walls in experimental conditions are not observed

  14. A new calculation method adapted to the experimental conditions for determining samples γ-activities induced by 14 MeV neutrons

    International Nuclear Information System (INIS)

    Rzama, A.; Erramli, H.; Misdaq, M.A.

    1994-01-01

    Induced gamma-activities of different disk shaped irradiated samples and standards with 14 MeV neutrons have been determined by using a Monte Carlo calculation method adapted to the experimental conditions. The self-absorption of the multienergetic emitted gamma rays has been taken into account in the final samples activities. The influence of the different activation parameters has been studied. Na, K, Cl and P contents in biological (red beet) samples have been determined. ((orig.))

  15. High-capacity neutron activation analysis facility

    International Nuclear Information System (INIS)

    Hochel, R.C.; Bowman, W.W.; Zeh, C.W.

    1980-01-01

    A high-capacity neutron activation analysis facility, the Reactor Activation Facility, was designed and built and has been in operation for about a year at one of the Savannah River Plant's production reactors. The facility determines uranium and about 19 other elements in hydrogeochemical samples collected in the National Uranium Resource Evaluation program, which is sponsored and funded by the United States Department of Energy, Grand Junction Office. The facility has a demonstrated average analysis rate of over 10,000 samples per month, and a peak rate of over 16,000 samples per month. Uranium is determined by cyclic activation and delayed neutron counting of the U-235 fission products; other elements are determined from gamma-ray spectra recorded in subsequent irradiation, decay, and counting steps. The method relies on the absolute activation technique and is highly automated for round-the-clock unattended operation

  16. Methodology for Quantitative Analysis of Large Liquid Samples with Prompt Gamma Neutron Activation Analysis using Am-Be Source

    International Nuclear Information System (INIS)

    Idiri, Z.; Mazrou, H.; Beddek, S.; Amokrane, A.

    2009-01-01

    An optimized set-up for prompt gamma neutron activation analysis (PGNAA) with Am-Be source is described and used for large liquid samples analysis. A methodology for quantitative analysis is proposed: it consists on normalizing the prompt gamma count rates with thermal neutron flux measurements carried out with He-3 detector and gamma attenuation factors calculated using MCNP-5. The relative and absolute methods are considered. This methodology is then applied to the determination of cadmium in industrial phosphoric acid. The same sample is then analyzed by inductively coupled plasma (ICP) method. Our results are in good agreement with those obtained with ICP method.

  17. Advances in 14 MeV neutron activation analysis by means of a new intense neutron source

    International Nuclear Information System (INIS)

    Pepelnik, R.; Fanger, H.-U.; Michaelis, W.; Anders, B.

    1982-01-01

    A new intense 14 MeV neutron generator with cylindrical acceleration structure has been put in operation at the GKSS Research Center Geesthacht. The sealed neutron tube is combined with a fast pneumatic rabbit system with particular capabilities for neutron activation analysis involving short-lived reaction products. The sample transfer time is less than 140 ms. The maximum neutron flux available for activation is 5.2x10 10 n/cm 2 s. Theoretical sensitivity predictions made in a previous study have been verified for some important trace elements. As a first application, samples of freeze-dried suspended matter and fishes of the Elbe river were analyzed. (author)

  18. Utilization of neutrons in nuclear data measurements and bulk sample analysis

    International Nuclear Information System (INIS)

    Jonah, S. A.

    1995-01-01

    Experimental investigations were carried out with neutrons in the fields of neutron data measurements and bulk sample analysis based on the interactions of neutron interactions required in the investigations together with some salient features of the sources employed are enumerated. Excitation cross section curves and isomeric cross section ratio of 58 Ni(n,p) 58 Co m , g reaction over the neutron energy range of between 5 and 15 MeV were determined using the activation analysis technique in combination with high-resolution gamma spectroscopy. Characteristics of the incident neutrons produced via the D-T reaction of a neutron generator and D-D reaction of a cyclotron were determined experimentally to account for the contributing effects of background neutrons especially in the 5-13 MeV neutron energy range where existing data are scanty and rather discrepant. The measured data agree well with calculated data using nuclear models but deviate significantly from the recommended data based on existing literature data. The measured δ act and δ m /δ g data made it possible to determine the cross section curve for 58 Ni(n,p) 58 Co m reaction. Furthermore the flux density distributions of thermal and primary fast neutrons in different configurations of bulk samples consisting of water, graphite and coal together with the attenuation characteristics were determined by the activation analysis and pulse height response spectrometry techniques. From the results obtained, an experimental geometry has been proposed for on-line elemental analysis of coal and other minerals. Similarly the total hydrogen content and 0+C/H atomic ratio in household and motor oils as well as crude oil samples of different origins were measured by an improved experimental arrangement based on the thermal neutron reflection technique. A detection limit of 0.12 w % was obtained for hydrogen indicating the possible adaptation of this technique for quality control of petroleum products

  19. Determination of traces of lithium in biological, environmental and metal samples by neutron activation analysis

    International Nuclear Information System (INIS)

    Yang, J.Y.; Tseng, C.L.; Lo, J.M.; Yang, M.H.

    1985-01-01

    Lithium in environmental, biological and metal samples was determined by neutron activation analysis via the 6 Li(n,α)T and 16 O(T,n) 18 F reactions. The samples were converted to aqueous solutions either by dissolution or by digestion and their aliquots were irradiated in a nuclear reactor for 2 h. The irradiated sample solution, was placed in a ZrO 2 column on which the 18 F nuclide was adsorbed. Most of the coexisting nuclides 24 Na, 82 Br, 38 Cl, 64 Cu, etc. were separated by elution with pH 1proportional3 solution. The column was subjected to a Ge(Li) detector for γ-ray spectrometry. The lithium content in the sample was estimated from the 18 F activity obtained. The matrix effect can be eliminated by either strong dilution of the samples in aqueous medium or by the method of standard addition. Lithium can be determined with high precision and accuracy in sub-ppm samples. (orig.) [de

  20. Analysis of toxical element in the whitening cream cosmetic samples using neutron activation analysis (NAA)

    International Nuclear Information System (INIS)

    Th Rina M; Sunarko

    2007-01-01

    Neutron activation analysis has been done to analyze of toxical elements that is not allowed in the whitening cream cosmetic. These samples have been randomly selected from the cosmetic market. The samples were irradiated at thermal neutron flux of 10"1"33n.cm"-"2s"-"1 in the irradiation facility of rabbit system in the RSG-GAS reactor Serpong. Counting of irradiated samples have been done by a high resolution HPGe detector couple to multichannel analyzer. Data have been analyzed by GENIE 2000. The sample have been qualitatively determined up to 19 elements. These elements are: As, Br, Ce, Co, Cr, Cs, Eu, Fe, Hg, K, La, Na, Rb, Sb, Se, Sc, Rb, Th, IV, and Zn. The result of qualitative analysis showed that the toxical elements present in the samples are Hg, As, Cr and Sb with the following concentration ranges in μg/g 25.2-65.1, 1.0-6.3, 30.5-89.1 and 2.9-5.3, respectively and these element not allowed in the whitening cream cosmetic. Besides that, the others elements have been detected in the samples are Br, Fe, Zn, Sc and Co, with concentration ranges, 13.1-36.4, 65.6-159.3, 0.79-77.1, 0.5-19.5, and 6.8-31.7 μg/g, respectively, in the sample whitening cream cosmetic. (author)

  1. 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)

  2. Neutron activation analysis in minerals prospecting

    International Nuclear Information System (INIS)

    Gomez, H.; Duque O, J.

    1988-01-01

    One method multielemental analysis in geological samples has been developed by neutron activation analysis without using standards and by eliminating many of the error sources of the absolute method. It uses the ratio of the activities induced by mass unit, between the element in the sample and one cobalt monitor. The detection limits are good for more than thirty elements in many prospecting programs, with a standard deviation less than 7%. The neutron flux used is 2x10 11 nxcm -2 .S -1 and the HPGE detector has a relative efficiency of 20% and an energy resolution of 1.9 KeV in 1332 KeV photopeak

  3. Activation measurements for fast neutrons. Part E. Evaluation of fast neutron 63Ni transmission factors

    International Nuclear Information System (INIS)

    Egbert, Stephen D.

    2005-01-01

    The 63 Ni measurements for fast neutrons in copper samples are compared to the calculated free-in-air 63 Ni neutron activation given in Chapter 3 by use of transmission factors. Transmission factors were calculated to account for the modification of the fluence and activation at each sample's in situ location. For the purposes of this discussion, the transmission factor (TF) is defined as the ratio of the in situ sample activation divided by the untilted free-in-air (FIA) activation at a height of 1 m above ground at the same ground range. Examples of the application of TF's will be provided in this section. (author)

  4. A neutron irradiator to perform nuclear activation

    International Nuclear Information System (INIS)

    Zamboni, C. B.; Zahn, G.S.; Figueredo, A. M. G.; Madi, T. F.; Yoriyaz, H.; Lima, R. B.; Shtejer, K.; Dalaqua Jr, L.

    2001-01-01

    The development of appropriate nuclear instrumentation to perform neutron activation analyze (NAA), using thermal and fast neutrons, can be useful to investigate materials outside the reactor premises. Considering this fact, a small size neutron irradiator prototype was developed at IPEN facilities (Instituto de Pesquisas Energeticas e Nucleares - Brazil). Basically, this prototype consists of a cylinder of 1200 mm long and 985 mm diameter (filled with paraffin) with two Am-Be sources (600GBq each) arranged in the longitudinal direction of its geometric center. The material to be irradiated is positioned at a radial direction of the cylinder between the two Am-Be sources. The main advantage of this irradiator is a very stable neutron flux eliminating the use of standard material (measure of the induced activity in the sample by comparative method). This way the process became agile, practical and economic, but quantities at mg levels of samples are necessary to achieve good sensitivity, when the material has a low microscopy neutron cross section. As fast and thermal neutron can be used, the flux distribution, for both, were calculated and the prototype performance is discussed

  5. Sample container for neutron activation analysis

    International Nuclear Information System (INIS)

    Lersmacher, B.; Verheijke, M.L.; Jaspers, H.J.

    1983-01-01

    The sample container avoids contaminating the sample substance by diffusion of foreign matter from the wall of the sample container into the sample. It cannot be activated, so that the results of measurements are not falsified by a radioactive container wall. It consists of solid carbon. (orig./HP) [de

  6. Study on the determination of palladium in biological samples by the method of neutron activation analysis

    International Nuclear Information System (INIS)

    Cavalcante, Cassio Queiroz

    2007-01-01

    Palladium is one of platinum group elements present in the nature at very low concentrations. However with the use of this element in the automobile catalyzers Pd became a new pollutant. Besides, Pd has been studied in the preparation of new antitumour drugs. Consequently, there is a need to determine Pd concentrations in biological and environmental samples. This study presents palladium results obtained in the analysis of biological samples and reference materials using instrumental thermal and epithermal neutron activation analysis (INAA and ENAA). The solvent extraction and solid phase extraction separation methods were also applied before ENAA. The samples analyzed in this study were, reference material BCR 723 - Palladium, Platinum and Rhodium in road dust, CCQM-P63 automotive catalyst material of the Proficiency Test and bovine tissue samples containing palladium prepared in the laboratory. Samples and palladium synthetic standard were irradiated at the IEA-R1 nuclear research reactor under thermal neutron flux of about 4 x 10 12 n cm-2 s-1, during a period of 4 and 16 h for INAA and ENAA, respectively. The induced gamma activity of 109 Pd to the sample and standard was measured using a hyper pure Ge detector coupled to a gamma ray spectrometer. The palladium concentration was calculated by comparative method. The gamma ray energy of 109 Pd radioisotope measured was of 88.0 keV, located in a spectrum region of low energy where occurs the interference of X rays, 'Bremsstrahlung' radiations, as well as Compton effect of 24 Na. The pre-separation of palladium from interfering elements by solvent extraction was performed using dimethylglyoxime complexant and chloroform as diluent. In the case of the pre separation procedure using solid reversed phase column, the palladium was retained using N,N-diethyl-N'-benzoyl thiourea complexant and eluted using ethanol. Aliquots of the resulting solutions from the pre-separations, free of interfering elements, were

  7. Neutron activation analysis of 127I and 129I environmental samples

    International Nuclear Information System (INIS)

    Takeishi, Minoru; Namiki, Atsushi; Ishida, Junichiro; Iwai, Makoto

    1987-01-01

    The analytical method of 127 I and 129 I in environmental samples has been studied and the background levels of these nuclides in soils, seaweeds and milk were measured. The analytical method consists of the combustion technique and neutron activation analysis (N.A.A.). The iodine was separated from samples by ignition at about 1,000 deg C in a quartz combustion apparatus with an oxygen and a nitrogen stream, and was absorbed by small amounts of active charcoal. The iodine was then purified through the carbontetrachloride extraction method and the PdI 2 decomposition method. Irradiation was conducted by JRR-4 (n th : 8 x 10 13 n/cm 2 · sec) for 40 min. After irradiation, the iodine was purified by the solvent extraction method same as pre-irradiation extraction. Each activity of 126 I and 130 I, which was produced by 127 I(n,2n) 126 I and 129 I(n,γ) 130 I reaction respectively, was measured by γ-spectrometry using a Ge-detector. The lower detection limits of 129 I by this method were 4 x 10 -7 Bq/g for dry soil, 7 x 10 -8 Bq/g for fresh seaweeds and 7 x 10 -6 Bq/l for fresh milk, respectively. The relative standard deviation of 129 I measurements in soil and milk were less than 10 %. (author)

  8. Neutron activation analysis

    International Nuclear Information System (INIS)

    Borsaru, M.; Eisler, P.L.

    1981-01-01

    A method of simultaneously analysing the aluminium and silicon content of a sample of material is claimed. The method comprises the following steps: (1) irradiating the sample with fast neutrons; (2) monitoring the thermal neutron flux within the sample; (3) monitoring the gamma radiation from the irradiated sample at energies of 1.78 MeV and 1.015 and/or 0.844 MeV; (4) using the monitored gamma radiation at 1.015 and/or 0.844 MeV to estimate the aluminium content of the sample; and (5) using the monitored gamma radiation at 1.78 MeV, compensated by the gamma radiation at 1.78 MeV due to the thermal neutron reaction with the estimated aluminium in the sample to estimate the silicon content

  9. Collection of size fractionated particulate matter sample for neutron activation analysis in Japan

    International Nuclear Information System (INIS)

    Otoshi, Tsunehiko; Nakamatsu, Hiroaki; Oura, Yasuji; Ebihara, Mitsuru

    2004-01-01

    According to the decision of the 2001 Workshop on Utilization of Research Reactor (Neutron Activation Analysis (NAA) Section), size fractionated particulate matter collection for NAA was started from 2002 at two sites in Japan. The two monitoring sites, ''Tokyo'' and ''Sakata'', were classified into ''urban'' and ''rural''. In each site, two size fractions, namely PM 2-10 '' and PM 2 '' particles (aerodynamic particle size between 2 to 10 micrometer and less than 2 micrometer, respectively) were collected every month on polycarbonate membrane filters. Average concentrations of PM 10 (sum of PM 2-10 and PM 2 samples) during the common sampling period of August to November 2002 in each site were 0.031mg/m 3 in Tokyo, and 0.022mg/m 3 in Sakata. (author)

  10. Different methodologies in neutron activation to approach the full analysis of environmental and nutritional samples

    International Nuclear Information System (INIS)

    Freitas, M.C.; Dionisio, I.; Dung, H.M.

    2008-01-01

    Different methodologies of neutron activation analysis (NAA) are now available at the Technological and Nuclear Institute (Sacavem, Portugal), namely Compton suppression, epithermal activation, replicate and cyclic activation, and low energy photon measurement. Prompt gamma activation analysis (PGAA) will be implemented soon. Results by instrumental NAA and PGAA on environmental and nutritional samples are discussed herein, showing that PGAA - carried out at the Institute of Isotope Research (Budapest, Hungary) - brings about an effective input to assessing relevant elements. Sensitivity enhancement in NAA by Compton suppression is also illustrated. Through a judicious combination of methodologies, practically all elements of interest in pollution and nutrition terms can be determined. (author)

  11. Calibration of neutron yield activation measurements at JET using MCNP and furnace neutron transport codes

    International Nuclear Information System (INIS)

    Pillon, M.; Martone, M.; Verschuur, K.A.; Jarvis, O.N.; Kaellne, J.

    1989-01-01

    Neutron transport calculations have been performed using fluence ray tracing (FURNACE code) and Monte Carlo particle trajectory sampling methods (MCNP code) in order to determine the neutron fluence and energy distributions at different locations in the JET tokamak. These calculations were used to calibrate the activation measurements used in the determination of the absolute fusion neutron yields from the JET plasma. We present here the neutron activation response coefficients calculated for three different materials. Comparison of the MCNP and FURNACE results helps identify the sources of error in these neutron transport calculations. The accuracy of these calculations was tested by comparing the total 2.5 MeV neutron yields derived from the activation measurements with those obtained with calibrated fission chambers; agreement at the ±15% level was demonstrate. (orig.)

  12. Neutron activation analysis for uranium and associated elements

    International Nuclear Information System (INIS)

    Bowman, W.W.

    1977-01-01

    The samples obtained by the Savannah River Laboratory as part of the National Uranium Resource Evaluation program are activated in the intense neutron flux from a Savannah River Plant production reactor. A pilot-scale facility was installed at the reactor site to provide analyses of samples through the initial phase of the program and to develop design data for a full-scale facility. Sediments are analyzed by direct activation of 0.5-g samples. However, to analyze ground or surface water samples, mineral elements from 1-liter samples are concentrated on ion exchange resin and then approximately 5-g samples of resin are activated. Uranium concentration is determined by counting neutrons emitted from specific short-lived products of fission induced in 235 U by the primary neutron flux. Repetitive short cycles of irradiation and counting permit detection and determination of <0.1 μg of uranium. Elements associated with uranium are determined by spectral analysis of the gamma ray activities induced by the cyclic and subsequent longer irradiations. The pilot facility consists of four irradiation positions (plus 2 spare positions), a sample loader and unloader, and counting stations with neutron and gamma ray detectors, all interconnected with a pneumatic sample transport system. A computer controls both the transport system and the data acquisition devices. Gamma ray counting data are stored on magnetic tape for further processing by a large central computer. Facility hardware and software are described. Repetitive analyses of standards have shown an accuracy within +-10% for uranium values and within +-25% for associated elements. A quality assurance program has been developed to maintain these levels of reliability

  13. Sample to moderator volume ratio effects in neutron yield from a PGNAA setup

    Energy Technology Data Exchange (ETDEWEB)

    Naqvi, A.A. [Department of Physics, King Fahd University of Petroleum and Minerals, KFUPM Box 1815, Dhahran-31261 (Saudi Arabia)]. E-mail: aanaqvi@kfupm.edu.sa; Fazal-ur-Rehman [Department of Physics, King Fahd University of Petroleum and Minerals, KFUPM Box 1815, Dhahran-31261 (Saudi Arabia); Nagadi, M.M. [Department of Physics, King Fahd University of Petroleum and Minerals, KFUPM Box 1815, Dhahran-31261 (Saudi Arabia); Khateeb-ur-Rehman [Department of Physics, King Fahd University of Petroleum and Minerals, KFUPM Box 1815, Dhahran-31261 (Saudi Arabia)

    2007-02-15

    Performance of a prompt gamma ray neutron activation analysis (PGNAA) setup depends upon thermal neutron yield at the PGNAA sample location. For a moderator, which encloses a sample, thermal neutron intensity depends upon the effective moderator volume excluding the void volume due to sample volume. A rectangular moderator assembly has been designed for the King Fahd University of Petroleum and Minerals (KFUPM) PGNAA setup. The thermal and fast neutron yield has been measured inside the sample cavity as a function of its front moderator thickness using alpha particle tracks density and recoil proton track density inside the CR-39 nuclear track detectors (NTDs). The thermal/fast neutron yield ratio, obtained from the alpha particle tracks density to proton tracks density ratio in the NTDs, shows an inverse correlation with sample to moderator volume ratio. Comparison of the present results with the previously published results of smaller moderators of the KFUPM PGNAA setup confirms the observation.

  14. Application of neutron activation analysis for the determination of essential elements in egg samples

    International Nuclear Information System (INIS)

    Gomes, Bruna G.; Maihara, Vera A.; Avegliano, Roseane P.

    2013-01-01

    The eggs are among the twenty foods consumed by the population of the five major regions of Brazil. Among the types of eggs, there are differences in nutritional value, which can vary according to the food of the bird. This study evaluating the elements Cl, K, Mg, Mn and Na considered essential micronutrients in food, because they are fundamental in several metabolic processes necessary for the maintenance and training of the human body. We analyzed three types of eggs: egg whites, of the quail, and the colonial in cooked and raw form, using the Instrumental Neutron Activation Analysis method (INAA). The egg samples were lyophilized and pulverized before analysis. To validate the methodology, reference materials NIST RM 8415 Whole Egg Powder and NIST SRM 1567 Wheat Flour were analyzed. The samples, reference materials and standards of the elements were irradiated for 20 seconds under a thermal neutron flux of 6,6x10 12 cm -2 s -1 in the nuclear research reactor IEA-R1 of IPEN-CNEN / SP. The results were consistent with the values of the Brazilian Table of Food Composition (TACO)

  15. Determination of chromium in water samples by neutron activation analysis after preconcentration on activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    van der Sloot, H A [Stichting Reactor Centrum Nederland, Petten

    1977-01-01

    A method is presented for the determination of chromium in sea- and fresh water. Chromium is concentrated on activated carbon from a neutral solution after a previous reduction of chromate with sodium sulfite at pH 1.5. The adsorption conditions, acidity, concentrations, amount of carbon, stirring-time, sample-volume, salinity, the influence of storage on the ratio of tervalent to hexavalent chromium, were investigated. The final determination of the total chromium content is performed by instrumental neutron-activation analysis. By preconcentration on activated carbon, a differentiation between tervalent and hexavalent chromium is possible. A separate determination of both species is not yet feasible due to the high carbon blank and to the necessity of measuring the adsorption percentage on carbon. The lower limit of determination, which depends on the value of the carbon blank, is 0.05 ..mu..g Cr/l with a precision of 20%. The determination is hampered by the considerable blank from the carbon. The use of activated carbon prepared from recrystallized sugar will probably improve the lower limit of determination and possibly allow the determination of chromate.

  16. Activation neutron detector

    International Nuclear Information System (INIS)

    Ambardanishvili, T.S.; Kolomiitsev, M.A.; Zakharina, T.Y.; Dundua, V.J.; Chikhladze, N.V.

    1976-01-01

    An activation neutron detector made as a moulded and cured composition of a material capable of being neutron-activated is described. The material is selected from a group consisting of at least two chemical elements, a compound of at least two chemical elements and their mixture, each of the chemical elements and their mixture, each of the chemical elements being capable of interacting with neutrons to form radioactive isotopes having different radiation energies when disintegrating. The material capable of being neutron-activated is distributed throughout the volume of a polycondensation resin inert with respect to neutrons and capable of curing. 17 Claims, No Drawings

  17. Irradiation test of HAFM and tag gas samples at the standard neutron field of 'YAYOI'

    International Nuclear Information System (INIS)

    Iguchi, Tetsuo

    1997-03-01

    To check the accuracy of helium accumulation neutron fluence monitors (HAFM) as new technique for fast reactor neutron dosimetry and the applicability of tag gas activation analysis to fast reactor failed fuel detection, their samples were irradiated at the standard neutron field of the fast neutron source reactor 'YAYOI' (Nuclear Engineering Research Laboratory, University of Tokyo). Since October in 1996, the HAFM samples such as 93% enriched boron (B) powders of 1 mg and natural B powders of 10 mg contained in vanadium (V) capsule were intermittently irradiated at the reactor core center (Glory hole: Gy) and/or under the leakage neutron field from the reactor core (Fast column: FC). In addition, new V capsules filled with enriched B of 40 mg and Be of 100 mg, respectively, were put into an experimental hole through the blanket surrounding the core. These neutron fields were monitored by the activation foils consisting of Fe, Co, Ni, Au, 235 U, 237 Np etc., mainly to confirm the results obtained from 1995's preliminary works. In particular, neutron flux distributions in the vicinity of irradiated samples were measured in more detail. At the end of March in 1997, the irradiated neutron fluence have reached the goal necessary to produce the detectable number of He atoms more than ∼10 13 in each HAFM sample. Six kinds of tag gas samples, which are the mixed gases of isotopically adjusted Xe and Kr contained in SUS capsules, were separately irradiated three times at Gy under the neutron fluence of ∼10 16 n/cm 2 in average. After irradiation, γ-ray spectra were measured for each sample. Depending on the composition of tag gas mixtures, the different patterns of γ-ray peak spectra from 79 Kr, 125 Xe, etc. produced through tag gas activation were able to be clearly identified. These experimental data will be very useful for the benchmark test of tag gas activation calculation applied to the fast reactor failed fuel detection. (author)

  18. Rare earths analysis of rock samples by instrumental neutron activation analysis, internal standard method

    International Nuclear Information System (INIS)

    Silachyov, I.

    2016-01-01

    The application of instrumental neutron activation analysis for the determination of long-lived rare earth elements (REE) in rock samples is considered in this work. Two different methods are statistically compared: the well established external standard method carried out using standard reference materials, and the internal standard method (ISM), using Fe, determined through X-ray fluorescence analysis, as an element-comparator. The ISM proved to be the more precise method for a wide range of REE contents and can be recommended for routine practice. (author)

  19. Methods for preparing comparative standards and field samples for neutron activation analysis of soil

    International Nuclear Information System (INIS)

    Glasgow, D.C.; Dyer, F.F.; Robinson, L.

    1995-01-01

    One of the more difficult problems associated with comparative neutron activation analysis (CNAA) is the preparation of standards which are tailor-made to the desired irradiation and counting conditions. Frequently, there simply is not a suitable standard available commercially, or the resulting gamma spectrum is convoluted with interferences. In a recent soil analysis project, the need arose for standards which contained about 35 elements. In response, a computer spreadsheet was developed to calculate the appropriate amount of each element so that the resulting gamma spectrum is relatively free of interferences. Incorporated in the program are options for calculating all of the irradiation and counting parameters including activity produced, necessary flux/bombardment time, counting time, and appropriate source-to-detector distance. The result is multi-element standards for CNAA which have optimal concentrations. The program retains ease of use without sacrificing capability. In addition to optimized standard production, a novel soil homogenization technique was developed which is a low cost, highly efficient alternative to commercially available homogenization systems. Comparative neutron activation analysis for large scale projects has been made easier through these advancements. This paper contains details of the design and function of the NAA spreadsheet and innovative sample handling techniques. (author) 7 refs.; 5 tabs

  20. Methods for preparing comparative standards and field samples for neutron activation analysis of soil

    International Nuclear Information System (INIS)

    Glasgow, D.C.; Dyer, F.F.; Robinson, L.

    1994-01-01

    One of the more difficult problems associated with comparative neutron activation analysis (CNAA) is the preparation of standards which are tailor-made to the desired irradiation and counting conditions. Frequently, there simply is not a suitable standard available commercially, or the resulting gamma spectrum is convoluted with interferences. In a recent soil analysis project, the need arose for standards which contained about 35 elements. In response, a computer spreadsheet was developed to calculate the appropriate amount of each element so that the resulting gamma spectrum is relatively free of interferences. Incorporated in the program are options for calculating all of the irradiation and counting parameters including activity produced, necessary flux/bombardment time, counting time, and appropriate source-to-detector distance. The result is multi-element standards for CNAA which have optimal concentrations. The program retains ease of use without sacrificing capability. In addition to optimized standard production, a novel soil homogenization technique was developed which is a low cost, highly efficient alternative to commercially available homogenization systems. Comparative neutron activation analysis for large scale projects has been made easier through these advancements. This paper contains details of the design and function of the NAA spreadsheet and innovative sample handling techniques

  1. Application of the neutron activation analysis method to the multielemental determination of food samples

    International Nuclear Information System (INIS)

    Maihara, V.A.

    1985-01-01

    The application of thermal neutron activation analysis method for determining elements presented at low concentration and level of traces in bread and dried milk samples, using non-destructive and chemical analyses, was studied. The non-destructive analyses were based on measurements of gamma spectrometry of samples and standards irradiated by thermal neutron flux on the order of 10 12 n cm -2 s -1 . The irradiation time varied from some minutes to 8 hours. The Na, Cl, Mn, Br, Fe, Zn, Rb, Sb, Cr and Sc elements in bread samples were determined. The Na, K, Cl, Ca, Mg, Br, Al, Zn, Rb, Sb and Cr elements in dried milk samples were determined. In destructive analysis, the 24 Na radioisotope was separeted by retention on hydrated antimony pentoxide column from 8N HCL after digestion of organic matter. The bread was dissolved in HNO 3 concentrated and 70% of HCLO 4 and the dried milk was dissolved in HNO 3 concentrated and H 2 O 2 . The 64 Cu, 69m Zn and 140 La radioisotopes determined. The concentrations obtained for dried milk were compared with data obtained by other authors from different contries. Basic considerations on detection limit related to its application on the technique used in this work, were done. The detection limits and trace elements using the Currie and Girardi methods were determined. The accuracy of results obtained for trace element detection limits is discussed. (Author) [pt

  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. Activation analysis of rare-earth elements in opium and cannabis samples. [Neutron reactions

    Energy Technology Data Exchange (ETDEWEB)

    Henke, G [Muenster Univ. (Germany, F.R.). Inst. fuer Pharmazeutische Chemie

    1977-01-01

    Rare-earth concentrations in 65 Opium, Cannabis and Cannabis resin samples seized from various parts of the world were determined by destructive NAA. Because of the greater concentrations of Ca, P, K, Fe, Na and Si in plant materials, rare-earth elements were isolated after neutron irradiation and determined by gamma-spectrometry. The main steps of the method are: Preashing of 1 g Cannabis resin, 2.5 g Cannabis, or 7.5 g Opium, respectively, in quartz ampoules (5 h, 500 deg C). Neutron irradiation, 24 h at 5x10/sup 13/n cm/sup -2/sec/sup -1/. Cooling period 2-3 days. After addition of 0.1 ..mu..Ci /sup 139/Ce and rare-earth carriers wet ashing of irradiated samples with H/sub 2/SO/sub 4//HNO/sub 3/, followed by alternate addition of HNO/sub 3/ and H/sub 2/O/sub 2/ (30%). Precipitation and removal of silicates, precipitation of fluorides, precipitation of hydroxides. Dissolution of hydroxides in HCl. Extraction with di-(2-ethylhexyl)phosphate (DEHP)/toluene and twice back-extraction of rare earths, gamma-spectrometry of HCl phase. Due to sample activity and half-life of nuclides, three measurements were made on each sample: 2 days (for La, Sm, Gd, Ho, Er, Yb); 14 days (for Nd, Lu) and 30 days after irradiation (for Ce, Eu, Tb). Great variations in absolute element concentrations, but only small significant differences of rare earth concentration ratios were found, indicating inconsiderable biogeochemical fractionation. The mean values of these ratios correspond to the relative abundances of the rare earths in the upper continental earth's crust.

  4. An Assessment of Elemental Compositions and Concentrations in a Marble Sample from Hatnub Area using Internal Mono Standard Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Soliman, N.F.; EL-Shershaby, A.; EL-Bahi, S.; Walley El-Dine, N.; Abd El-Halim, E.S.; Afifi, S.

    2012-01-01

    A marble sample was taken from Hatnub area near Asyot, where a high pollution is expected. The sample was specially treated and prepared for elemental analysis using the k 0 -based internal mono standard neutron activation analysis . The irradiation facility of the first Egyptian Training Research Reactor (ETRR-1) was used to irradiate the sample together with gold and zirconium monitor samples. The pneumatic irradiation rabbit system (PIRS) built in the vertical thermal column of the second Egyptian Training Research Reactor (ETRR-2) was used to irradiate another weight of the marble sample and a sample from a certificated reference material JB-1 for short time irradiation. A new method was developed to measure the thermal to epithermal neutron flux ratio and the deviation in the real epithermal neutron spectrum ( 1/E 1±a lpha ) from the ideal (1/E ). The elemental analysis was carried out by high-resolution gamma-ray spectrometry. The accuracy of the internal mono standard method has been evaluated by analyzing the JB-1 certified reference material

  5. Forensic neutron activation analysis - the Japanese scene

    International Nuclear Information System (INIS)

    Kishi, Tohru.

    1986-01-01

    The progress of forensic neutron activation analysis/FNAA/ in Japan is described. FNAA began in 1965 and during the past 20 years many cases have been handled; these include determination of toxic materials, comparison examination of physical evidences /e.g.,paints, metal fragments, plastics and inks/ and drug sample differenciation. Neutron activation analysis is applied routinely to the scientific criminal investigation as one of multielement analytical techniques. This paper also discusses these routine works. (author)

  6. Neutron activation system for spectral measurements of pulsed ion diode neutron production

    International Nuclear Information System (INIS)

    Hanson, D.L.; Kruse, L.W.

    1980-02-01

    A neutron energy spectrometer has been developed to study intense ion beam-target interactions in the harsh radiation environment of a relativistic electron beam source. The main component is a neutron threshold activation system employing two multiplexed high efficiency Ge(Li) detectors, an annihilation gamma coincidence system, and a pneumatic sample transport. Additional constraints on the neutron spectrum are provided by total neutron yield and time-of-flight measurements. A practical lower limit on the total neutron yield into 4π required for a spectral measurement with this system is approx. 10 10 n where the neutron yield is predominantly below 4 MeV and approx. 10 8 n when a significant fraction of the yield is above 4 MeV. Applications of this system to pulsed ion diode neutron production experiments on Hermes II are described

  7. Neutron activation analysis of geological material

    International Nuclear Information System (INIS)

    Greef, G.J.

    1977-05-01

    In neutron activation analysis the precision and accuracy of results are often misleading, since only the statistical errors which accompany the measuring of radioactivity are taken into consideration. Several other factors can, however, also influence precision and accuracy. It was found that a geological sample was contaminated with the construction material of the mill in which it had been pulverised. Several geometrical differences which could possibly play a role were also investigated. Impurities in the irradiation containers affect the determination of some elements in the samples; the contamination materials in quarts irradiation tubes were determined. The flux gradients which may effect the relative activities of the samples and standards were measured. Suitable standards are necessary to ensure accurate analyses of geological material. Available natural standards were critically evaluated and several methods were investigated by which synthetic standards may be prepared. In order to accurately determine gallium, lanthanum and samarium by means of neutron activation analysis, sodium first had to be removed. After irradiation the sample was dissolved in a mixture of acids and the soidium absorbed from the solution on a hydrated antimony pentoxide column. Gallium, lanthanum and samarium activities were measured by means of precision gamma-spectrometry

  8. Automated facility for analysis of soil samples by neutron activation, counting, and data control

    International Nuclear Information System (INIS)

    Voegele, A.L.; Jesse, R.H.; Russell, W.L.; Baker, J.

    1978-01-01

    An automated facility remotely and automatically analyzes soil, water, and sediment samples for uranium. The samples travel through pneumatic tubes and switches to be first irradiated by neutrons and then counted for resulting neutron and gamma emission. Samples are loaded into special carriers, or rabbits, which are then automatically loaded into the pneumatic transfer system. The sample carriers have been previously coded with an identification number, which can be automatically read in the system. This number is used for correlating and filing data about the samples. The transfer system, counters, and identification system are controlled by a network of microprocessors. A master microprocessor initiates routines in other microprocessors assigned to specific tasks. The software in the microprocessors is unique for this type of application and lends flexibility to the system

  9. Neutron activation analysis of Etruscan pottery

    International Nuclear Information System (INIS)

    Whitehead, J.; Silverman, A.; Ouellet, C.G.; Clark, D.D.; Hossain, T.Z.

    1992-01-01

    Neutron activation analysis (NAA) has been widely used in archaeology for compositional analysis of pottery samples taken from sites of archaeological importance. Elemental profiles can determine the place of manufacture. At Cornell, samples from an Etruscan site near Siena, Italy, are being studied. The goal of this study is to compile a trace element concentration profile for a large number of samples. These profiles will be matched with an existing data bank in an attempt to understand the place of origin for these samples. The 500 kW TRIGA reactor at the Ward Laboratory is used to collect NAA data for these samples. Experiments were done to set a procedure for the neutron activation analysis with respect to sample preparation, selection of irradiation container, definition of activation and counting parameters and data reduction. Currently, we are able to analyze some 27 elements in samples of mass 500 mg with a single irradiation of 4 hours and two sequences of counting. Our sensitivity for many of the trace elements is better than 1 ppm by weight under the conditions chosen. In this talk, details of our procedure, including quality assurance as measured by NIST standard reference materials, will be discussed. In addition, preliminary results from data treatment using cluster analysis will be presented. (author)

  10. Trace elements detection in whole food samples by Neutron Activation Analysis, k0-method

    International Nuclear Information System (INIS)

    Sathler, Márcia Maia; Menezes, Maria Ângela de Barros Correia; Salles, Paula Maria Borges de

    2017-01-01

    Inorganic elements, from natural and anthropogenic sources are present in foods in different concentrations. With the increase in anthropogenic activities, there was also a considerable increase in the emission of these elements in the environment, leading to the need of monitoring the elemental composition of foods available for consumption. Numerous techniques have been used to detect inorganic elements in biological and environmental matrices, always aiming at reaching lower detection limits in order to evaluate the trace element content in the sample. Neutron activation analysis (INAA), applying the k 0 -method, produces accurate and precise results without the need of chemical preparation of the samples – that could cause their contamination. This study evaluated the presence of inorganic elements in whole foods samples, mainly elements on trace levels. For this purpose, seven samples of different types of whole foods were irradiated in the TRIGA MARK I IPR-R1 research reactor - located at CDTN/CNEN, in Belo Horizonte, MG. It was possible to detect twenty two elements above the limit of detection in, at least, one of the samples analyzed. This study reaffirms the INAA, k 0 - method, as a safe and efficient technique for detecting trace elements in food samples. (author)

  11. Neutron activation analysis for certification of standard reference materials

    International Nuclear Information System (INIS)

    Capote Rodriguez, G.; Perez Zayas, G.; Hernandez Rivero, A.; Ribeiro Guevara, S.

    1996-01-01

    Neutron activation analysis is used extensively as one of the analytical techniques in the certification of standard reference materials. Characteristics of neutron activation analysis which make it valuable in this role are: accuracy multielemental capability to asses homogeneity, high sensitivity for many elements, and essentially non-destructive method. This paper report the concentrations of 30 elements (major, minor and trace elements) in four Cuban samples. The samples were irradiated in a thermal neutron flux of 10 12- 10 13 n.cm 2. s -1. The gamma ray spectra were measured by HPGe detectors and were analyzed using ACTAN program development in Center of Applied Studies for Nuclear Development

  12. Instrumental neutron activation analysis of some fossil samples from Romanian palaeolontologic sites

    International Nuclear Information System (INIS)

    Pantelica, A. I.; Salagean, M. N.; Scarlat, A. G.; Georgescu, I. I.; Murariu-Magureanu, M.D

    2001-01-01

    During the fossilization process, elemental contents of the buried materials are modified by different physical, chemical and biological factors, such as ground water flow and degree of aeration, chemical composition of the soil, bacterial activity, the process being influenced by the climatical conditions. Bone tissue, by the calcium phosphate mineral (hydroxyapatite) in the external part and organic component (fat and collagen) in the inner part, has proved to be a proper substrate for minor elements accumulation. The uniform increasing of certain elemental concentrations during the fossilization process is generally used in palaeoscience for the age dating. Instrumental neutron activation analysis (INAA) method was used by us to determine Al, As, Au, Ba, Br, Ca, Co, Cr, Cs, Fe, Hf, K, Mg, Mn, Na, Ni, Rb, Sb, Sc, Se, Sr, Th, U, V, Zn, and of the rare earth elements Ce, Eu, La, Lu, Nd, Sm, Tb, Yb contents of two different fossil materials discovered in Romania during 1995-1996: Elephas primigenius mammoth mandible bone (1.5-2 million years age) and Pecten solarium shell (20-25 million years age). Mammoth mandible bone samples were taken both from the external and the internal part of the bone. Shell fragments were taken in association with the surrounding rock samples. Irradiations were carried out at the WWR-S reactor in Bucharest (neutron fluence rate 2.3 x 10 12 cm -2 s -1 and at the TRIGA reactor in Pitesti (neutron fluence rate 5 x 10 13 cm -2 s -1 . For the mammoth mandible bone (relative high contents of U and P) corrections were done for the uranium fission and (n,γ)β - contribution to Ce, La, Nd and Sm concentrations, and for the phosphorus interference in Al determination. It was taken into account that 141 Ce, 140 La, 147 Nd, 153 Sm isotopes are originated not only by the neutron activation reactions of these elements, but also from the beta - decay chains of the uranium fission products; for 153 Sm, spectral interference with 103.65 keV X-ray of 239

  13. Minimization of the blank values in the neutron activation analysis of biological samples considering the whole procedure

    International Nuclear Information System (INIS)

    Lux, F.; Bereznai, T.; Haeberlin, T.H.

    1986-01-01

    In our determination of trace element contents of animal tissue by neutron activation analysis in the course of structure-activity relationship studies on platinum containing cancer drugs and wound healing we have tried to minimize the blank values that are caused by different sources of contamination during surgery, sampling and the activation analysis procedure. The following topics have been investigated: the abrasions from scalpels made of stainless steel, titanium or quartz; the type of surgery; the homogenisation of the samples before irradiation by use of a ball milll; the surface contaminations of the quartz ampoules that pass into the digestion solution of the irradiated samples. The appropriate measures taken in order to reduce the blank values are described. The results of analyses performed under these conditions indicate the effectiveness of the given measures, especially shown by the low values obtained for the chromium contents of the analysed muscle samples. (author)

  14. Elemental analysis of two Egyptian iron ores and produced industrial iron samples by neutron activation analysis

    International Nuclear Information System (INIS)

    Sroor, A.; Abdel-Basset, N.; Abdel-Haleem, A.S.; Hassan, A.M.

    2001-01-01

    Elemental analysis of two iron ores and initial industrial iron production prepared by the Egyptian Iron and Steel Company of Helwan near Cairo were performed by the instrumental neutron activation analysis technique. Five samples of each type were irradiated for 48 h in a thermal neutron flux of 4x10 12 n/cm 2 s in the first Egyptian research reactor ET-RR-1. Also, the Pneumatic Irradiation Rabbit System (PIRS), attached to the reactor ET-RR-1 in Inshass, was used to measure short-life elements. The γ-ray spectra were obtained with a hyper pure germanium detection system. The concentration percentage values of major, minor and trace elements are presented. Implications of the elemental concentration values obtained are presented

  15. Multielemental analysis of Brazilian milk powder and bread samples by neutron activation

    International Nuclear Information System (INIS)

    Maihara, V.A.; Vasconcellos, M.B.A.

    1988-01-01

    The concentrations of Na, Cl, Mn, Br, Fe, Zn, Rb, Sb, Sc, Cr, Al and Mg were determined in some types of bread and in some brands of milk powder consumed in the city of Sao Paulo (SP - Brasil), by instrumental neutron activation analysis. Radiochemical separations were carried out by means of retention of 24 Na on hydrated antimony pentoxide (HAP) from a 8N HCl solution, after digestion of the organic matter. Thus the radioisotopes 64 Cu, 69m Zn and 140 La could be determined in the effluent solution. The detection limits of the trace elements analyzed in bread and milk powder samples were determined using the Currie and Girardi criterions. (author) 22 refs.; 2 figs.; 7 tabs

  16. Determination of Mineral Contents in Unpolished Rice and Bean Samples by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Moon, J. H.; Kim, S. H.; Baek, S. Y.; Chung, Y. S.

    2012-01-01

    As scientists have focused their researches on the health impacts caused by mineral nutrient deficiencies and hazardous elements, public concern regarding mineral intake from dietary food is rising. In this reason, the dietary habits of Koreans have been shifted from white rice to more nutrient rice like unpolished rice and rice mixed with beans. It is known that unpolished rice and beans contain more protein, vitamin and mineral contents than white rice and are more beneficial to human health, even though they sometimes cause indigestion or allergy. The objectives of this study were to determine the mineral contents in unpolished rice and bean samples by a neutron activation analysis (NAA) and to compare the level of mineral contents between the samples

  17. Determination of Mineral Contents in Unpolished Rice and Bean Samples by Neutron Activation Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Moon, J. H.; Kim, S. H.; Baek, S. Y.; Chung, Y. S. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2012-05-15

    As scientists have focused their researches on the health impacts caused by mineral nutrient deficiencies and hazardous elements, public concern regarding mineral intake from dietary food is rising. In this reason, the dietary habits of Koreans have been shifted from white rice to more nutrient rice like unpolished rice and rice mixed with beans. It is known that unpolished rice and beans contain more protein, vitamin and mineral contents than white rice and are more beneficial to human health, even though they sometimes cause indigestion or allergy. The objectives of this study were to determine the mineral contents in unpolished rice and bean samples by a neutron activation analysis (NAA) and to compare the level of mineral contents between the samples

  18. The verification of neutron activation analysis support system (cooperative research)

    Energy Technology Data Exchange (ETDEWEB)

    Sasajima, Fumio; Ichimura, Shigeju; Ohtomo, Akitoshi; Takayanagi, Masaji [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Sawahata, Hiroyuki; Ito, Yasuo [Tokyo Univ. (Japan). Research Center for Nuclear Science and Technology; Onizawa, Kouji [Radiation Application Development Association, Tokai, Ibaraki (Japan)

    2000-12-01

    Neutron activation analysis support system is the system in which even the user who has not much experience in the neutron activation analysis can conveniently and accurately carry out the multi-element analysis of the sample. In this verification test, subjects such functions, usability, precision and accuracy of the analysis and etc. of the neutron activation analysis support system were confirmed. As a method of the verification test, it was carried out using irradiation device, measuring device, automatic sample changer and analyzer equipped in the JRR-3M PN-3 facility, and analysis software KAYZERO/SOLCOI based on the k{sub 0} method. With these equipments, calibration of the germanium detector, measurement of the parameter of the irradiation field and analysis of three kinds of environmental standard sample were carried out. The k{sub 0} method adopted in this system is primarily utilized in Europe recently, and it is the analysis method, which can conveniently and accurately carried out the multi-element analysis of the sample without requiring individual comparison standard sample. By this system, total 28 elements were determined quantitatively, and 16 elements with the value guaranteed as analytical data of the NIST (National Institute of Standards and Technology) environment standard sample were analyzed in the accuracy within 15%. This report describes content and verification result of neutron activation support system. (author)

  19. Fast-neutron activation analysis of manganese nodules

    International Nuclear Information System (INIS)

    Michaelis, W.; Fanger, H.U.; Mueller, A.; Pepelnik, R.

    1976-01-01

    The present paper describes the development of a new nuclear method that allows rapid determinations of the most relevant metals Ni and Cu without sample treatment, thus being particularly suited for quasi-continuous elemental analyses in mining and processing. The measurement is based on fast-neutron activation using Cockcroft-Walton generators, sealed neutron tubes or, possibly, (α,n)-type natural sources. Fast-neutron activation of manganese nodules is dominated by the (n,p)-reactions on Si, Al, Fe; the (n,α)-reaction on Mn and the (n,2n)-reaction on Cu. By choosing appropriate irradiation and cooling periods gamma-ray activities with comparatively simple spectral distributions are induced. From these spectra the Mn/Fe ratio in the nodules can be determined without the elaborate procedures usually required in absolute methods for eliminating systematic errors from fluctuations in sample and/or irradiation parameters. It is connected with the absolute Ni and Cu contents via well-known geochemical correlations which according to a lot of statistical data apply to quite different deposits and nodule types in the Pacific. Using these correlations the determination of the most important metals reduces to the evaluation of a peak area ratio. Measurements of the neutron flux distribution and the apparent sample density are unnecessary. The simple structure of the spectra allows the application of detectors with modest energy resolution, e.g. scintillation counters which can be manufactured as ruggedized crystal assemblies with great resistance to thermal and mechanical shock. The method is described in detail and possible interference, in particular from thermal and epithermal neutrons, are discussed. (orig.) [de

  20. Measurement of neutron activation in concrete samples

    International Nuclear Information System (INIS)

    Zagar, T.; Ravnik, M.

    2000-01-01

    The results of activation studies of ordinary and barytes concrete samples relevant for research reactor decommissioning are given. Five important long-lived radioactive isotopes ( 54 Mn, 60 Co, 65 Zn, 133 Ba, and 152 Eu) were identified from the gamma-ray spectra measured in the irradiated concrete samples. Activation of these samples was also calculated using ORIGEN2 code. Comparison of calculated and measured results is given. (author)

  1. 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

  2. Particulate matter and neutron activation analysis

    International Nuclear Information System (INIS)

    Otoshi, Tsunehiko

    2003-01-01

    In these years, economy of East Asian region is rapidly growing, and countries in this region are facing serious environmental problems. Neutron activation analysis is known as one of high-sensitive analytical method for multi elements. And it is a useful tool for environmental research, particularly for the study on atmospheric particulate matter that consists of various constituents. Elemental concentration represents status of air, such as emission of heavy metals from industries and municipal incinerators, transportation of soil derived elements more than thousands of kilometers, and so on. These monitoring data obtained by neutron activation analysis can be a cue to evaluate environment problems. Japanese government launched National Air Surveillance Network (NASN) employing neutron activation analysis in 1974, and the data has been accumulated at about twenty sampling sites. As a result of mitigation measure of air pollution sources, concentrations of elements that have anthropogenic sources decreased particularly at the beginning of the monitoring period. However, even now, concentrations of these anthropogenic elements reflect the characteristics of each sampling site, e.g. industrial/urban, rural, and remote. Soil derived elements have a seasonal variation because of the contribution of continental dust transported by strong westerly winds prevailing in winter and spring season. The health effects associated with trace elements in particulate matter have not been well characterized. However, there is increasing evidence that particulate air pollution, especially fine portion of particles in many different cities is associated with acute mortality. Neutron activation analysis is also expected to provide useful information to this new study field related to human exposures and health risk. (author)

  3. Investigation of Six Geological Samples From Wady Sitra Eastern Desert - Egypt Using K0 Neutron Activation Method

    International Nuclear Information System (INIS)

    Soliman, N.F.; Ashmawy, L.S.; Walley El-Dine, N.; Sroor, A.; Mohamed, T.El.

    2010-01-01

    k 0 - Neutron Activation Analysis (k 0 -NAA) is applied to investigate six geological samples collected from Wady Sitra at Eastern desert of Egypt during the survey of gold presence in this area. The samples together with a group of standard (Mo, Fe, Sb and W) are irradiated for 3 hours in one of the inner irradiation site of the Second Egyptian Training and Research Reactor (ETRR-2) operating at power of 19 MW. Mo, Fe and Sb are used to measure the neutron spectrum parameters α(epithermal non-ideality factor) and f (the thermal to epithermal flux ratio) while W is used to test the obtained results. The α( and f parameters are measured using the so-called bare triple monitor method and the obtained results was found to be f = 17.5 ± 0.35 and α(= 0.03±0.002. A Fortran computer program is designed and used to calculate the values of Q 0 (α)for the analyzed elements . The concentration values of 25 elements in the present rock samples have been presented

  4. Neutron activation analysis for noble metals in matte leach residues

    International Nuclear Information System (INIS)

    Hart, R.J.

    1978-01-01

    The development of the neutron activation analysis technique as a method for rapid and precise determinations of platinum group metals in matte leach residues depends on obtaining a method for effecting complete and homogeneous sample dilution. A simple method for solid dilution of metal samples is outlined in this study, which provided a basis for the accurate determination of all the noble metals by the Neutron Activation Analysis technique

  5. Active neutron multiplicity analysis and Monte Carlo calculations

    International Nuclear Information System (INIS)

    Krick, M.S.; Ensslin, N.; Langner, D.G.; Miller, M.C.; Siebelist, R.; Stewart, J.E.; Ceo, R.N.; May, P.K.; Collins, L.L. Jr

    1994-01-01

    Active neutron multiplicity measurements of high-enrichment uranium metal and oxide samples have been made at Los Alamos and Y-12. The data from the measurements of standards at Los Alamos were analyzed to obtain values for neutron multiplication and source-sample coupling. These results are compared to equivalent results obtained from Monte Carlo calculations. An approximate relationship between coupling and multiplication is derived and used to correct doubles rates for multiplication and coupling. The utility of singles counting for uranium samples is also examined

  6. The multielement potential of fast neutron cyclic activation analysis

    International Nuclear Information System (INIS)

    Nonie, S.E.; Randle, K.

    1994-01-01

    Cyclic neutron activation analysis (CNAA) has, in recent years been developed as a useful analytical tool for the assay of short-lived isotopes in single element situations. The work described in this paper investigates the potential of the technique for composite samples having a wide range of elements that produce short-lived and long-lived isotopes on neutron irradiation. Accelerator-derived neutrons with average energies of 3 MeV, 6 MeV and 14 MeV were employed in what has been dubbed 'Fast Neutron Cyclic Neutron Activation Analysis' (FNCAA). The approach to multi-element analysis entailed: determination of cycle parameters in single element samples via the reactions 27 Al(n,p) 27 Mg(9.6 min,E γ =840keV), and 137 Ba(n,n 'γ137m Ba(2.3 min,E γ 137m Ba(2.3 min,E γ =662 keV), a test of the method on a composite rock sample, determination of analytical sensitivities using both powdered kale and rock standards and a comparison of analytical results with other techniques. The results obtained in all these measurements are presented and discussed. (author) 10 refs.; 3 figs.; 5 tabs

  7. Active-interrogation measurements of fast neutrons from induced fission in low-enriched uranium

    International Nuclear Information System (INIS)

    Dolan, J.L.; Marcath, M.J.; Flaska, M.; Pozzi, S.A.; Chichester, D.L.; Tomanin, A.; Peerani, P.

    2014-01-01

    A detection system was designed with MCNPX-PoliMi to measure induced-fission neutrons from U-235 and U-238 using active interrogation. Measurements were then performed with this system at the Joint Research Centre in Ispra, Italy on low-enriched uranium samples. Liquid scintillators measured induced fission neutrons to characterize the samples in terms of their uranium mass and enrichment. Results are presented to investigate and support the use of organic liquid scintillators with active interrogation techniques to characterize uranium containing materials. -- Highlights: • We studied low-enriched uranium using active-interrogation experiments including a deuterium–tritium neutron generator and an americium–lithium isotopic neutron source. • Liquid scintillators measured induced-fission neutrons from the active-interrogation methods. • Fast-neutron (DT) and thermal-neutron (Am–Li) interrogation resulted in the measurement of trends in uranium mass and 235 U enrichment respectively. • MCNPX-PoliMi, the Monte Carlo transport code, simulated the measured induced-fission neutron trends in the liquid scintillators

  8. Active-interrogation measurements of fast neutrons from induced fission in low-enriched uranium

    Energy Technology Data Exchange (ETDEWEB)

    Dolan, J.L., E-mail: jldolan@umich.edu [Department of Nuclear Engineering and Radiological Sciences, University of Michigan, Ann Arbor, MI 48109 (United States); Marcath, M.J.; Flaska, M.; Pozzi, S.A. [Department of Nuclear Engineering and Radiological Sciences, University of Michigan, Ann Arbor, MI 48109 (United States); Chichester, D.L. [Idaho National Laboratory, Idaho Falls, ID 83415 (United States); Tomanin, A.; Peerani, P. [European Commission, Joint Research Centre, Institute for Transuranium Elements, Ispra (Italy)

    2014-02-21

    A detection system was designed with MCNPX-PoliMi to measure induced-fission neutrons from U-235 and U-238 using active interrogation. Measurements were then performed with this system at the Joint Research Centre in Ispra, Italy on low-enriched uranium samples. Liquid scintillators measured induced fission neutrons to characterize the samples in terms of their uranium mass and enrichment. Results are presented to investigate and support the use of organic liquid scintillators with active interrogation techniques to characterize uranium containing materials. -- Highlights: • We studied low-enriched uranium using active-interrogation experiments including a deuterium–tritium neutron generator and an americium–lithium isotopic neutron source. • Liquid scintillators measured induced-fission neutrons from the active-interrogation methods. • Fast-neutron (DT) and thermal-neutron (Am–Li) interrogation resulted in the measurement of trends in uranium mass and {sup 235}U enrichment respectively. • MCNPX-PoliMi, the Monte Carlo transport code, simulated the measured induced-fission neutron trends in the liquid scintillators.

  9. Activation Measurements for Thermal Neutrons, U.S. Measurements of 36Cl in Mineral Samples from Hiroshima and Nagasaki; and Measurement of 63 Ni in Copper Samples From Hiroshima by Accelerator Mass Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Tore Straume; Alfredo A. Marchetti; Stephen D. Egbert; James A. Roberts; Ping Men; Shoichiro Fujita; Kiyoshi Shizuma; Masaharu Hoshi; G. Rugel; W. Ruhm; G. Korschinek; J. E. McAninch; K. L. Carroll; T. Faestermann; K. Knie; R. E. Martinelli; A. Wallner; C. Wallner

    2005-01-14

    The present paper presents the {sup 36}Cl measurement effort in the US. A large number of {sup 36}Cl measurements have been made in both granite and concrete samples obtained from various locations and distances in Hiroshima and Nagasaki. These measurements employed accelerator mass spectrometry (AMS) to quantify the number of atoms of {sup 36}Cl per atom of total Cl in the sample. Results from these measurements are presented here and discussed in the context of the DS02 dosimetry reevaluation effort for Hiroshima and Nagasaki atomic-bomb survivors. The production of {sup 36}Cl by bomb neutrons in mineral samples from Hiroshima and Nagasaki was primarily via the reaction {sup 35}Cl(n,{gamma}){sup 36}Cl. This reaction has a substantial thermal neutron cross-section (43.6 b at 0.025 eV) and the product has a long half-life (301,000 y). hence, it is well suited for neutron-activation detection in Hiroshima and Nagasaki using AMS more than 50 years after the bombings. A less important reaction for bomb neutrons, {sup 39}K(n,{alpha}){sup 36}Cl, typically produces less than 10% of the {sup 36}Cl in mineral samples such as granite and concrete, which contain {approx} 2% potassium. In 1988, only a year after the publication of the DS86 final report (Roesch 1987), it was demonstrated experimentally that {sup 36}Cl measured using AMS should be able to detect the thermal neutron fluences at the large distances most relevant to the A-bomb survivor dosimetry. Subsequent measurements in mineral samples from both Hiroshima and Nagasaki validated the experimental findings. The potential utility of {sup 36}Cl as a thermal neutron detector in Hiroshima was first presented by Haberstock et al. who employed the Munich AMS facility to measure {sup 36}Cl/Cl ratios in a gravestone from near the hypocenter. That work subsequently resulted in an expanded {sup 36}Cl effort in Germany that paralleled the US work. More recently, there have also been {sup 36}Cl measurements made by a Japanese

  10. Measurement of arsenic in sectioned hair samples by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Guinn, V.P.; Gavrilas-Guinn, M.; Demiralp, R.

    1994-01-01

    In a recent Texas murder case, bundles of head hair from the female victim (aligned with all root ends together) were washed, cut into 7 mm sections, air-dried and weighed, activated in a nuclear reactor neutron flux, and then counted with a Ge(Li) detector/4096-channel gamma-ray spectrometer. In each of the 15 samples, the 559 keV gamma-ray peak of 26.3 hour 76 As was measured. In the section closest to the scalp, an arsenic concentration of 107 ppm was found (cf. a 'normal' level of about 1 ppm As). Barium ingestion was also possible so Ba was looked for, but not found. The victim's husband was found guilty of murder by chronic arsenic poisoning. (author) 2 refs.; 1 fig.; 1 tab

  11. Analysis of some egyptian cosmetic samples by using fast neutron activation analysis

    International Nuclear Information System (INIS)

    Medhat, M.E.; Hassan, M.F.; Ali, M.A.; Awaad, Z.

    2002-01-01

    A description of our neutron generator (NG) facility for neutron activation analysis is presented. As an example, the concentration of Na, Mg, Al, Si, K, Cl, Ca and Fe elements were determined in two domestic brands of face powder by using a beam of 14 MeV neutrons. An empirical expression for detector efficiency in terms of incident gamma ray energy and the source-detector distance has been obtained for a hyper pure germanium detector (HPGe) using different standard point sources. The comparison of the calculated efficiencies and the measured values in the energy range from 59.5 to 1332.2 keV and for source-to-detector distances of 5-30 cm show the agreement between the calculated values and the measured experimental values

  12. Trace determination of uranium and thorium in biological samples by radiochemical neutron activation analysis

    International Nuclear Information System (INIS)

    Benedik, Ljudmila; Repinc, Urska; Byrne, Anthony R.; Stegnar, Peter

    2002-01-01

    Radiochemical neutron activation analysis (RNAA) is an excellent method for determining uranium and thorium; it offers unique possibilities for their ultratrace analysis using selective radiochemical separations. Regarding the favourably sensitive nuclear characteristics of uranium and of thorium with respect to RNAA, but the different half-lives of their induced nuclides, two different approaches were used. In the first approach uranium and thorium were determined separately via 239 U, 239 Np and 233 Pa. In the second approach these elements were 239 239 233 determined simultaneously in a single sample using U and/or Np and Pa. Isolation of induced nuclides was based on separation by extraction and/or anion exchange chromatography. Chemical yields were measured in each sample aliquot using added 235 U, 238 Np and 231 Pa radioisotopic tracers. (author)

  13. Neutron activation determination of noble metals in samples of terrestrial and cosmic origin using microfire assay concentration

    International Nuclear Information System (INIS)

    Kolesov, G.M.; Sapozhnikov, D.Yu.

    1995-01-01

    The effects of various factors (composition of mixture, relationship between the mass of mixture and sample, value of the Ni:S ratio, fusion time, and temperature) on the conditions of the fire assay concentration of the noble metals with nickel sulfide were investigated, and a method proposed for their quantitative separation from different geological matrices with a neutron activation determination for up to 10 -1 -10 -3 ppb. The proposed method is used to analyse geological samples, i.e. ores, stones, iron meteorites, chromites, soil and lunar rocks. (author)

  14. Use of CITATION code for flux calculation in neutron activation analysis with voluminous sample using an Am-Be source

    International Nuclear Information System (INIS)

    Khelifi, R.; Idiri, Z.; Bode, P.

    2002-01-01

    The CITATION code based on neutron diffusion theory was used for flux calculations inside voluminous samples in prompt gamma activation analysis with an isotopic neutron source (Am-Be). The code uses specific parameters related to the energy spectrum source and irradiation system materials (shielding, reflector). The flux distribution (thermal and fast) was calculated in the three-dimensional geometry for the system: air, polyethylene and water cuboidal sample (50x50x50 cm). Thermal flux was calculated in a series of points inside the sample. The results agreed reasonably well with observed values. The maximum thermal flux was observed at a distance of 3.2 cm while CITATION gave 3.7 cm. Beyond a depth of 7.2 cm, the thermal flux to fast flux ratio increases up to twice and allows us to optimise the detection system position in the scope of in-situ PGAA

  15. Minimization of the blank values in the neutron activation analysis of biological samples considering the whole procedure

    International Nuclear Information System (INIS)

    Lux, F.; Bereznai, T.; Trebert Haeberlin, S.

    1987-01-01

    During the determination of trace element contents of animal tissue by neutron activation analysis in the course of structure-activity relationship studies on platinum containing cancer drugs and wound healing the authors tried to minimize the blank values that are caused by different sources of contamination during surgery, sampling and the activation analysis procedure. The following topics were investigated: abrasions from scalpels made of stainless steel, titanium or quartz, the type of surgery, the surface contaminations of the quartz ampoules, etc. The measures to be taken to reduce tha blank values are described. (author) 19 refs.; 4 tables

  16. Neutron activation diagnostics at the National Ignition Facility (invited)

    Energy Technology Data Exchange (ETDEWEB)

    Bleuel, D. L.; Yeamans, C. B.; Bernstein, L. A.; Bionta, R. M.; Caggiano, J. A.; Drury, O. B.; Hagmann, C. A.; Hatarik, R.; Knittel, K. M.; McNaney, J. M.; Moran, M.; Schneider, D. H. G. [Lawrence Livermore National Laboratory, Livermore, California 94550 (United States); Casey, D. T.; Frenje, J. A.; Johnson, M. Gatu [Massachusetts Institute of Technology Plasma Science and Fusion Center, Cambridge, Massachusetts 02139 (United States); Cooper, G. W. [University of New Mexico, Albuquerque, New Mexico 87131 (United States); Knauer, J. P. [Laboratory for Laser Energetics, University of Rochester, Rochester, New York 14623 (United States); Leeper, R. J.; Ruiz, C. L. [Sandia National Laboratory, Albuquerque, New Mexico 87185 (United States)

    2012-10-15

    Neutron yields are measured at the National Ignition Facility (NIF) by an extensive suite of neutron activation diagnostics. Neutrons interact with materials whose reaction cross sections threshold just below the fusion neutron production energy, providing an accurate measure of primary unscattered neutrons without contribution from lower-energy scattered neutrons. Indium samples are mounted on diagnostic instrument manipulators in the NIF target chamber, 25-50 cm from the source, to measure 2.45 MeV deuterium-deuterium fusion neutrons through the {sup 115}In(n,n'){sup 115m} In reaction. Outside the chamber, zirconium and copper are used to measure 14 MeV deuterium-tritium fusion neutrons via {sup 90}Zr(n,2n), {sup 63}Cu(n,2n), and {sup 65}Cu(n,2n) reactions. An array of 16 zirconium samples are located on port covers around the chamber to measure relative yield anisotropies, providing a global map of fuel areal density variation. Neutron yields are routinely measured with activation to an accuracy of 7% and are in excellent agreement both with each other and with neutron time-of-flight and magnetic recoil spectrometer measurements. Relative areal density anisotropies can be measured to a precision of less than 3%. These measurements reveal apparent bulk fuel velocities as high as 200 km/s in addition to large areal density variations between the pole and equator of the compressed fuel.

  17. Automatic sample changer control software for automation of neutron activation analysis process in Malaysian Nuclear Agency

    Science.gov (United States)

    Yussup, N.; Ibrahim, M. M.; Rahman, N. A. A.; Mokhtar, M.; Salim, N. A. A.; Soh@Shaari, S. C.; Azman, A.; Lombigit, L.; Azman, A.; Omar, S. A.

    2018-01-01

    Most of the procedures in neutron activation analysis (NAA) process that has been established in Malaysian Nuclear Agency (Nuclear Malaysia) since 1980s were performed manually. These manual procedures carried out by the NAA laboratory personnel are time consuming and inefficient especially for sample counting and measurement process. The sample needs to be changed and the measurement software needs to be setup for every one hour counting time. Both of these procedures are performed manually for every sample. Hence, an automatic sample changer system (ASC) that consists of hardware and software is developed to automate sample counting process for up to 30 samples consecutively. This paper describes the ASC control software for NAA process which is designed and developed to control the ASC hardware and call GammaVision software for sample measurement. The software is developed by using National Instrument LabVIEW development package.

  18. Neutron activation analysis of high-purity iron in comparison with chemical analysis

    International Nuclear Information System (INIS)

    Kinomura, Atsushi; Horino, Yuji; Takaki, Seiichi; Abiko, Kenji

    2000-01-01

    Neutron activation analysis of iron samples of three different purity levels has been performed and compared with chemical analysis for 30 metallic and metalloid impurity elements. The concentration of As, Cl, Cu, Sb and V detected by neutron activation analysis was mostly in agreement with that obtained by chemical analysis. The sensitivity limits of neutron activation analysis of three kinds of iron samples were calculated and found to be reasonable compared with measured values or detection limits of chemical analysis; however, most of them were above the detection limits of chemical analysis. Graphite-shielded irradiation to suppress fast neutron reactions was effective for Mn analysis without decreasing sensitivity to the other impurity elements. (author)

  19. Determination of neodymium and gadolinium in geologic samples by neutron activation analysis

    International Nuclear Information System (INIS)

    Souza, M.A. de; Marques, L.S.

    1982-07-01

    The determination of Nd and Gd present in rocks by neutron activation analysis is aimed at. A separation procedure for the rare earth group of elements is presented. The method is based on the retention of 233 Pa, 182 Ta and 46 Sc by hydrated antimony pentoxide (HAP) in a 6M HClO 4 medium. Those radioisotopes are interferences in the gamma-ray spectrum of 153 Gd and 147 Nd. The reliability of the method was tested by means of the geological standards BCR-1 and G-2 from the U.S. Geological Survey. The limitations of the instrumental neutron activation analysis and the advantages of the chemical separation are discussed for the special case of the Nd and Gd determinations. (Author) [pt

  20. Trace elements detection in whole food samples by Neutron Activation Analysis, k{sub 0}-method

    Energy Technology Data Exchange (ETDEWEB)

    Sathler, Márcia Maia; Menezes, Maria Ângela de Barros Correia, E-mail: maia.sathler@gmail.com, E-mail: menezes@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil); Salles, Paula Maria Borges de, E-mail: pauladesalles@yahoo.com.br [Universidade Federal de Minas Gerais (DEN/UFMG), Belo Horizonte, MG (Brazil). Departamento de Engenharia Nuclear

    2017-07-01

    Inorganic elements, from natural and anthropogenic sources are present in foods in different concentrations. With the increase in anthropogenic activities, there was also a considerable increase in the emission of these elements in the environment, leading to the need of monitoring the elemental composition of foods available for consumption. Numerous techniques have been used to detect inorganic elements in biological and environmental matrices, always aiming at reaching lower detection limits in order to evaluate the trace element content in the sample. Neutron activation analysis (INAA), applying the k{sub 0}-method, produces accurate and precise results without the need of chemical preparation of the samples – that could cause their contamination. This study evaluated the presence of inorganic elements in whole foods samples, mainly elements on trace levels. For this purpose, seven samples of different types of whole foods were irradiated in the TRIGA MARK I IPR-R1 research reactor - located at CDTN/CNEN, in Belo Horizonte, MG. It was possible to detect twenty two elements above the limit of detection in, at least, one of the samples analyzed. This study reaffirms the INAA, k{sub 0} - method, as a safe and efficient technique for detecting trace elements in food samples. (author)

  1. Neutron activation determination of gold in technogenic raw materials with different mineral composition

    Directory of Open Access Journals (Sweden)

    Yudakov Aleksandr A.

    2015-01-01

    Full Text Available The methods used to determine the gold content in the technogenic objects of gold mining were analyzed regarding their non-homogeneity and complexity of chemical and mineral compositions. A possible application of the neutron activation analysis with the use of the californium source of neutrons for determining the content of fine-grained and extra-fine-grained gold in the technogenic objects, including the bottom-ash waste of energy providers, is considered. It was demonstrated that the chemical composition of the sample affects the neuron flux distribution in the sample, which can essentially distort the results of the neutron activation analysis. In order to eliminate possible systematic errors investigations of the effect of the sample mineral composition on the results of the gold determination using the neutron activation analysis were carried out. Namely, a large mass of rock (3-5 kg was loaded into an activation zone using four matrix types such as silicate, carbon-containing, iron-containing, and titanium magnetite. It was shown that there wereno significant difference between the dispersal of the fluxes of thermal and resonance neutrons emitted from 252Cf during activation of the gold-containing technogenic samples with different mineral compositions.

  2. A comparative study of 232Th and 238U activity estimation in soil samples by gamma spectrometry and Neutron Activation Analysis (NAA) technique

    International Nuclear Information System (INIS)

    Rekha, A.K.; Anilkumar, S.; Narayani, K.; Babu, D.A.R.

    2012-01-01

    Radioactivity in the environment is mainly due to the naturally occurring radionuclides like uranium, thorium with their daughter products and potassium. Even though Gamma spectrometry is the most commonly used non destructive method for the quantification of these naturally occurring radionuclides, Neutron Activation Analysis (NAA), a well established analytical technique, can also be used. But the NAA technique is a time consuming process and needs proper standards, proper sample preparation etc. In this paper, the 232 Th and 238 U activity estimated using gamma ray spectrometry and NAA technique are compared. In the case of direct gamma spectrometry method, the samples were analysed after sealing in a 250 ml container. Whereas for the NAA, about 300 mg of each sample, after irradiation were subjected to gamma spectrometry. The 238 U and 232 Th activities (in Bq/kg) in samples were estimated after the proper efficiency correction and were compared. The estimated activities by these two methods are in good agreement. The variation in 238 U and 232 Th activity values are within ± 15% which are acceptable for environmental samples

  3. A high pressure sample facility for neutron scattering

    International Nuclear Information System (INIS)

    Carlile, C.J.; Glossop, B.H.

    1981-06-01

    Commissioning tests involving deformation studies and tests to destruction as well as neutron diffraction measurements of a standard sample have been carried out on the SERC high pressure sample facility for neutron scattering studies. A detailed description of the pressurising equipment is given. (author)

  4. Neutron activation analysis-comparative (NAAC)

    International Nuclear Information System (INIS)

    Zimmer, W.H.

    1979-01-01

    A software system for the reduction of comparative neutron activation analysis data is presented. Libraries are constructed to contain the elemental composition and isotopic nuclear data of an unlimited number of standards. Ratios to unknown sample data are performed by standard calibrations. Interfering peak corrections, second-order activation-product corrections, and deconvolution of multiplets are applied automatically. Passive gamma-energy analysis can be performed with the same software. 3 figures

  5. Neutron activation analysis of biological substances

    International Nuclear Information System (INIS)

    Ordogh, M.

    1978-08-01

    A Bowen cabbage sample was used as a reference material for the neutron activation studies, and the method was checked by the analysis of other biological substances (blood or serum etc.). For nondestructive measurements also some non-trace elements were determined in order to decide whether the activation analysis is a useful means for such measurements. The new activation analysis procedure was used for biomedical studies as, e.g., for trace element determination in body fluids, and for the analysis of inorganic components in air samples. (R.P.)

  6. Phosphorus determination in bone samples by activation analysis using fast neutrons

    International Nuclear Information System (INIS)

    Madi Filho, T.; Cunha, I.I.L.

    1992-01-01

    In this report, the phosphorus determination in animal bone samples was made by means of the irradiation of samples using 14 MeV neutron generator (Van de Graaff accelerator). Induced radiation in irradiated material was measured using a NaI(Tl) detector. The method was tested in a IAEA certified standard, being obtained the values of 15,48% and 15,75%. The content of phosphorus was obtained by using two different calculating methods. Based on the experiments performed it was possible to establish a method of phosphorus analysis in bone using the Van de Graaff accelerator. (author)

  7. The development of neutron activation, sample transportation and γ-ray counting routine system for numbers of geological samples

    International Nuclear Information System (INIS)

    Shibata Shin-nosuke; Tanaka, Tsuyoshi; Minami, Masayo

    2001-01-01

    A new gamma-ray counting and data processing system for non-destructive neutron activation analysis has been set up in Radioisotope Center in Nagoya University. The system carry out gamma-ray counting, sample change and data processing automatically, and is able to keep us away from parts of complicated operations in INAA. In this study, we have arranged simple analytical procedure that makes practical works easier than previous. The concrete flow is described from the reparation of powder rock samples to gamma-ray counting and data processing by the new INAA system. Then it is run over that the analyses used two Geological Survey of Japan rock reference samples JB-1a and JG-1a in order to evaluate how the new analytical procedure give any speediness and accuracy for analyses of geological materials. Two United States Geological Survey reference samples BCR-1 and G-2 used as the standard respectively. Twenty two elements for JB-1a and 25 elements for JG-1a were analyzed, the uncertainty are <5% for Na, Sc, Fe, Co, La, Ce, Sm, Eu, Yb, Lu, Hf, Ta and Th, and of <10% for Cr, Zn, Cs, Ba, Nd, Tb and U. This system will enable us to analyze more than 1500 geologic samples per year. (author)

  8. Pneumatic sample-transfer system for use with the Lawrence Livermore National Laboratory rotating target neutron source (RTNS-I)

    International Nuclear Information System (INIS)

    Williams, R.E.

    1981-07-01

    A pneumatic sample-transfer system is needed to be able to rapidly retrieve samples irradiated with 14-MeV neutrons at the Rotating Target Neutron Source (RTNS-I). The rabbit system, already in place for many years, has been refurbished with modern system components controlled by an LSI-11 minicomputer. Samples can now be counted three seconds after an irradiation. There are many uses for this expanded 14-MeV neutron activation capability. Several fission products difficult to isolate from mixed fission fragments can be produced instead through (n,p) or (n,α) reactions with stable isotopes. Mass-separated samples of Nd, Mo, and Se, for example, can be irradiated to produce Pr, Nb, and As radionuclides sufficient for decay scheme studies. The system may also be used for multielement fast-neutron activation analysis because the neutron flux is greater than 2 x 10 11 n/cm 2 -sec. Single element analyses of Si and O are also possible. Finally, measurements of fast-neutron cross sections producing short-lived activation products can be performed with this system. A description of the rabbit system and instructions for its use are presented in this report

  9. The determination of chromium in water samples by neutron activation analysis after preconcentration on activated carbon

    International Nuclear Information System (INIS)

    Sloot, H.A. van der

    1977-01-01

    A method is presented for the determination of chromium in sea- and fresh water. Chromium is concentrated on activated carbon from a neutral solution after a previous reduction of chromate with sodium sulfite at pH 1.5. The adsorption conditions, acidity, concentrations, amount of carbon, stirring-time, sample-volume, salinity, the influence of storage on the ratio of tervalent to hexavalent chromium, were investigated. The final determination of the total chromium content is performed by instrumental neutron-activation analysis. By preconcentration on activated carbon, a differentiation between tervalent and hexavalent chromium is possible. A separate determination of both species is not yet feasible due to the high carbon blank and to the necessity of measuring the adsorption percentage on carbon. The lower limit of determination, which depends on the value of the carbon blank, is 0.05 μg Cr/l with a precision of 20%. The determination is hampered by the considerable blank from the carbon. The use of activated carbon prepared from recrystallized sugar will probably improve the lower limit of determination and possibly allow the determination of chromate. (T.G.)

  10. Practical considerations in instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Ahmad, N.

    2001-01-01

    Activation analysis is a technique of elemental analysis based on the measurement of characteristics radiation from radionuclides formed directly or indirectly by activation. The activation can be induced by bombarding the material with neutrons or charged particles or gamma rays. This is a well-accepted analytical technique for the determination of composition of complex materials. This technique is also sensitive at trace levels and is almost free from analytical interferences of matrix. It is used for multi-elemental determination in rocks, minerals, alloys, biological materials, geological samples, non-destructive analysis of materials and environmental samples such as water, air particulate matter, plants, soil, sediments and diets. This method is also used for production and measurements of radioisotopes in materials of known composition, for example, when radioactivation is used for nuclear reaction studies, for flux and beam intensity measurements for trace experiments and process quality control. In this article the parameters affecting the sensitivity of instrumental neutron activation analysis are briefly discussed. (author)

  11. Neutron cross-section determination in geological samples (U)

    International Nuclear Information System (INIS)

    Harris, J.M.; McDaniel, P.J.

    1982-01-01

    The Prompt Gamma Neutron Activation Analysis (PGAA) technique yields elemental composition data which can be used to calculate the macroscopic cross section for any sample. The Small Sample Reactivity Measurements (SSRM) technique yields the macroscopic thermal absorption directly. Experimentally, PGAA is somewhat more difficult because of the calibration and data handling than is SSRM. However, SSRM requires a mathematical model of the reactor which means a rather complicated analysis. Once the model and calibration are completed, data analysis is routine. The SSRM technique is production oriented. 9 figures

  12. Effects of sample and spectrum characteristics on cold and thermal neutron prompt gamma activation analysis in environmental studies of plants

    International Nuclear Information System (INIS)

    Robinson, L.; Zhao, L.

    2009-01-01

    Previous studies including the development of methods for the determination of carbon, nitrogen, and phosphorus in cattail using cold neutron prompt gamma activation (CNPGAA) and thermal neutron prompt gamma activation analysis (TNPGAA); evaluation of the precision and accuracy of these methods through the analysis of Standard Reference Materials (SRMs); and comparison of the sensitivity of CNPGAA to TNPGAA have been done in the CNPGAA and TNPGAA facilities at the National Institute of Standards and Technology (NIST). This paper integrates the findings from all of these prior studies and presents recommendations for the application of CNPGAA and TNPGAA in environmental studies of plants based on synergistic considerations of the effects of neutron energy, matrix factors such as chlorine content, Compton scattering, hydrogen content, sample thickness, and spectral interferences from Cl on the determination of C, N, and P. This paper also provides a new approach that simulates a sensitivity curve for an element of interest (S), which is a function of hydrogen content (X) and sample thickness (Y) as follows: S = aX + bY + c (where a, b, and c are constants). This approach has provided more accurate results from the analysis of SRMs than traditional methods and an opportunity to use models to optimize experimental conditions. (author)

  13. 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)

  14. Activation measurements for thermal neutrons. Part A. Cobalt (60Co) activation

    International Nuclear Information System (INIS)

    Kerr, George D.; Shizuma, Kiyoshi; Endo, Satoru; Maruyama, Takashi; Cullings, Harry M.; Komura, Kazuhisa; Okumura, Yutaka; Egbert, Stephen D.

    2005-01-01

    The 60 Co measurements at Hiroshima and Nagasaki were reviewed and compared with the results of the new DS02 calculations for the two cities. Some corrections were made to previously published data from the 1965 measurements of JNIRS, ground ranges of all of the 60 Co measurements were reviewed and new ground ranges were determined when possible by transforming sample coordinates to the new city maps for Hiroshima and Nagasaki, and transmission factors were investigated for a number of samples used in the 60 Co measurements. Transmission factors were not calculated for all samples used in the 60 Co measurements but some general rules were given for estimating transmission factors for these samples. Experimental measurements of the background 60 Co activity from environmental neutrons were also reviewed, and it was found that the 60 Co background from environmental neutrons was not an important factor in the 60 Co measurements of bomb-induced activity at either city. (J.P.N.)

  15. Interpretation of active neutron measurements by the heterogeneous theory

    International Nuclear Information System (INIS)

    Birkhoff, G.; Depraz, J.; Descieux, J.P.

    1979-01-01

    In this paper are presented results from a study on the application of the heterogeneous method for the interpretation of active neutron measurements. The considered apparatus consists out of a cylindrical lead pile, which is provided with two axial channels: a central channel incorporates an antimony beryllium photoneutron source and an excentric channel serves for the insertion of the sample to be assayed for fissionable materials contents. The mathematical model of this apparatus is the heterogeneous group diffusion theory. Sample and source channel are described by multigroup monopolar and dipolar sources and sinks. Monopolar sources take account of neutron production within energy group and in-scatter from upper groups. Monopolar sinks represent neutron removal by absorption within energy group and outscatter to lower groups. Dipol sources describe radial streaming of neutrons across the sample channel. Multigroup diffusion theory is applied throughout the lead pile. The strengths of the monopolar and dipolar sources and sinks are determined by linear extrapolation distances of azimuthal mean and first harmonic flux values at the channels' surface. In an experiment we may measure the neutrons leaking out of the lead pile and linear extrapolation distances at the channels' surface. Such informations are utilized for interpretation in terms of fission neutron source strengh and mean neutron flux values in the sample. In this paper we summarized the theoretical work in course

  16. Opportunities for innovation in neutron activation analysis

    International Nuclear Information System (INIS)

    Peter Bode

    2012-01-01

    Neutron activation laboratories worldwide are at a turning point at which new staff has to be found for the retiring pioneers from the 1960s-1970s. A scientific career in a well-understood technique, often characterized as 'mature' may only be attractive to young scientists if still challenges for further improvement and inspiring new applications can be offered. The strengths and weaknesses of neutron activation analysis (NAA) are revisited to identify opportunities for innovation. Position-sensitive detection of elements in large samples, Monte Carlo calculations replacing the use of standards, use of scintillator detectors and new deconvolution techniques for increasing the sensitivity are examples of challenging new roads in NAA. Material science provides challenges for the application of NAA in both bulk samples, ultrathin layers and ultrapure materials. (author)

  17. On the accuracy of protein determination in large biological samples by prompt gamma neutron activation analysis

    International Nuclear Information System (INIS)

    Kasviki, K.; Stamatelatos, I.E.; Yannakopoulou, E.; Papadopoulou, P.; Kalef-Ezra, J.

    2007-01-01

    A prompt gamma neutron activation analysis (PGNAA) facility has been developed for the determination of nitrogen and thus total protein in large volume biological samples or the whole body of small animals. In the present work, the accuracy of nitrogen determination by PGNAA in phantoms of known composition as well as in four raw ground meat samples of about 1 kg mass was examined. Dumas combustion and Kjeldahl techniques were also used for the assessment of nitrogen concentration in the meat samples. No statistically significant differences were found between the concentrations assessed by the three techniques. The results of this work demonstrate the applicability of PGNAA for the assessment of total protein in biological samples of 0.25-1.5 kg mass, such as a meat sample or the body of small animal even in vivo with an equivalent radiation dose of about 40 mSv

  18. On the accuracy of protein determination in large biological samples by prompt gamma neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Kasviki, K. [Institute of Nuclear Technology and Radiation Protection, NCSR ' Demokritos' , Aghia Paraskevi, Attikis 15310 (Greece); Medical Physics Laboratory, Medical School, University of Ioannina, Ioannina 45110 (Greece); Stamatelatos, I.E. [Institute of Nuclear Technology and Radiation Protection, NCSR ' Demokritos' , Aghia Paraskevi, Attikis 15310 (Greece)], E-mail: ion@ipta.demokritos.gr; Yannakopoulou, E. [Institute of Physical Chemistry, NCSR ' Demokritos' , Aghia Paraskevi, Attikis 15310 (Greece); Papadopoulou, P. [Institute of Technology of Agricultural Products, NAGREF, Lycovrissi, Attikis 14123 (Greece); Kalef-Ezra, J. [Medical Physics Laboratory, Medical School, University of Ioannina, Ioannina 45110 (Greece)

    2007-10-15

    A prompt gamma neutron activation analysis (PGNAA) facility has been developed for the determination of nitrogen and thus total protein in large volume biological samples or the whole body of small animals. In the present work, the accuracy of nitrogen determination by PGNAA in phantoms of known composition as well as in four raw ground meat samples of about 1 kg mass was examined. Dumas combustion and Kjeldahl techniques were also used for the assessment of nitrogen concentration in the meat samples. No statistically significant differences were found between the concentrations assessed by the three techniques. The results of this work demonstrate the applicability of PGNAA for the assessment of total protein in biological samples of 0.25-1.5 kg mass, such as a meat sample or the body of small animal even in vivo with an equivalent radiation dose of about 40 mSv.

  19. Determination of selenium in samples of concentrated of nickel plus cobalt using the analysis through activation with epi thermic neutron

    International Nuclear Information System (INIS)

    Capote Rodriguez, G.; Perez Zayas, G.; Hernandez Rivero, A.; Moreno Bermudez, G.; Ribeiro Guevara, S.; Arribere, M.A.; Molina Insfran, J.

    1997-01-01

    In this work, the concentration of selenium and other elements was determined. Seventeen samples of sulfides plus cobalt were used. Among the employed methods for such purpose, the analysis was made through neutronic activation, in its instrumental variants, and by means of the application of radiochemical separation. (author) [es

  20. Active Interrogation of Sensitive Nuclear Material Using Laser Driven Neutron Beams

    International Nuclear Information System (INIS)

    Favalli, Andrea; Roth, Markus

    2015-01-01

    An investigation of the viability of a laser-driven neutron source for active interrogation is reported. The need is for a fast, movable, operationally safe neutron source which is energy tunable and has high-intensity, directional neutron production. Reasons for the choice of neutrons and lasers are set forth. Results from the interrogation of an enriched U sample are shown.

  1. Aspects of Low Temperature Irradiation in Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Brune, D.

    1968-08-01

    Neutron irradiation of the sample while frozen in a cooling device inserted in a reactor channel has been carried out in the analysis of iodine in aqueous samples as well as of mercury in biological tissue and water. For the simultaneous irradiation of a large number of aqueous solutions the samples were arranged in a suitable geometry in order to avoid mutual flux perturbation effects. The influence of the neutron temperature on the activation process has been discussed. Potential applications of the low temperature irradiation technique are outlined

  2. Aspects of Low Temperature Irradiation in Neutron Activation Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Brune, D

    1968-08-15

    Neutron irradiation of the sample while frozen in a cooling device inserted in a reactor channel has been carried out in the analysis of iodine in aqueous samples as well as of mercury in biological tissue and water. For the simultaneous irradiation of a large number of aqueous solutions the samples were arranged in a suitable geometry in order to avoid mutual flux perturbation effects. The influence of the neutron temperature on the activation process has been discussed. Potential applications of the low temperature irradiation technique are outlined.

  3. Neutron activation studies on JET

    International Nuclear Information System (INIS)

    Loughlin, M.J.; Forrest, R.A.; Edwards, J.E.G.

    2001-01-01

    Extensive neutron transport calculations have been performed to determine the neutron spectrum at a number of points throughout the JET torus hall. The model has been bench-marked against a set of foil activation measurements which were activated during an experimental campaign with deuterium/tritium plasmas. The model can predict the neutron activation of the foils on the torus hall walls to within a factor of three for reactions with little sensitivity to thermal neutrons. The use of scandium foils with and without a cadmium thermal neutron absorber was a useful monitor of the thermal neutron flux. Conclusions regarding the usefulness of other foils for benchmarking the calculations are also given

  4. Elemental analysis and plant samples at el-Manzala lake by neutron activation analysis technique

    Energy Technology Data Exchange (ETDEWEB)

    Eissa, E A; Rofail, N B; Abdel-Haleem, A S; El-Abbady, W H; Hassan, A M [Arab Republic of Egypt, Atomic energy Authority, Reactor and Neutron Physiscs Department, Cairo (Egypt)

    1996-12-31

    A soil and a plant samples were taken from two locations, Bahr el-Bakar and Bahr Kados at the Manzala lake, where a high pollution is expected. The samples were especially treated and prepared for investigation by thermal neutron activation analysis (NAA). The irradiation facilities of the first egyptian research reactor (ET-R R-1) and the hyper pure germanium (HPGe) detection system were used for such a type of analysis. Among the 34 identified elements Fe, Co, As, Ru, Cd, Te, La, Sm, Eu, Tb, Hg, Th, and U are of a special significance because of their toxic deleterious impact to organisms. This work is a part of a research project concerning pollution studies on the river nile and some lakes of egypt. The data obtained in the present work stand as a reference basic record for any future follow up of the contamination level. 1 tab.

  5. Elemental analysis and plant samples at el-Manzala lake by neutron activation analysis technique

    International Nuclear Information System (INIS)

    Eissa, E.A.; Rofail, N.B.; Abdel-Haleem, A.S.; El-Abbady, W.H.; Hassan, A.M.

    1995-01-01

    A soil and a plant samples were taken from two locations, Bahr el-Bakar and Bahr Kados at the Manzala lake, where a high pollution is expected. The samples were especially treated and prepared for investigation by thermal neutron activation analysis (NAA). The irradiation facilities of the first egyptian research reactor (ET-R R-1) and the hyper pure germanium (HPGe) detection system were used for such a type of analysis. Among the 34 identified elements Fe, Co, As, Ru, Cd, Te, La, Sm, Eu, Tb, Hg, Th, and U are of a special significance because of their toxic deleterious impact to organisms. This work is a part of a research project concerning pollution studies on the river nile and some lakes of egypt. The data obtained in the present work stand as a reference basic record for any future follow up of the contamination level. 1 tab

  6. Introduction of sample environment equipment for neutron scattering experiments

    International Nuclear Information System (INIS)

    Shimojo, Yutaka; Ihata, Yoshiaki; Kaneko, Koji; Takeda, Masayasu

    2013-02-01

    Neutron scattering experiments have been frequently performed under variety of sample conditions, such as various temperatures, pressures, magnetic fields and stresses, and those complex conditions to fully utilize superior properties of neutron. To this aim, a number of sample environment equipment, refrigerators, furnaces, pressure cells, superconducting magnets are equipped in JRR-3 to be used for experiments. In this document, all available sample environment equipment in both JRR-3 reactor and guide halls are summarized. We hope this document would help neutron scattering users to perform effective and excellent experiments. (author)

  7. 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)

  8. Development of a radiochemical neutron activation analysis procedure for determination of rhenium in biological and environmental samples at ultratrace level

    Czech Academy of Sciences Publication Activity Database

    Kučera, Jan; Byrne, A. R.; Mizera, Jiří; Lučaníková, M.; Řanda, Zdeněk

    2006-01-01

    Roč. 269, č. 2 (2006), s. 251-257 ISSN 0236-5731 R&D Projects: GA ČR(CZ) GA203/04/0943 Institutional research plan: CEZ:AV0Z10480505 Keywords : radiochemical neutron activation analysis * rhenium * biological and environmental samples Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 0.509, year: 2006

  9. The determination of fast neutron fluence in radiation stability tests of steel samples

    International Nuclear Information System (INIS)

    Hogel, J.; Vespalec, R.

    1979-01-01

    The activation method is described of determining fast neutron fluence. Samples of steel designed for WWER type reactor pressure vessels were irradiated in the CHOUCA-rigs in the core of the WWR-S reactor. The neutron spectrum was measured by the multiple activation foil method and the effective cross sections of fluence monitors were calculated. The fluences obtained from the reactions 54 Fe(n,p) 54 Mn and 63 Cu(n,α) 60 Co are presented and the method is discussed. (author)

  10. Determination of selenium in roasted beans coffee samples consumed in Algeria by radiochemical neutron activation analysis method

    International Nuclear Information System (INIS)

    Messaoudi, Mohammed; Begaa, Samir; Hamidatou, Lylia; Salhi, M'hamed

    2018-01-01

    The essential trace element selenium is a focus of attention due to its effects on human health, there being consequences of both its deficiency and excess. Due to the ultra-trace content of selenium, the neutron activation analysis method (NAA) is difficult to apply. We therefore made use of the radiochemical neutron activation analysis (RNAA) to determine Se at low level concentrations in several consumed food items in Algeria. A radiochemical procedure based on liquid-liquid separation was established in our laboratory. In this research we focused on the determination of selenium in two species of coffee: Arabica and Robusta. The accuracy of the method was assessed by analyzing the certified reference material NIST-SRM 1573a (tomato leaves). The results obtained show a selenium variation from 0.025 to 0.052 μg/g in coffee beans and an average yield of the separation of about 85%. The results of this study were compared with those obtained with samples from Brazilian, Caribbean, Indian and Kenyan coffee beans.

  11. Determination of trace gold in rocks and minerals by neutron activation analysis

    International Nuclear Information System (INIS)

    Zhao Yunlong; Zhou Suqing; Liang Yutang

    1988-05-01

    The determination of trace gold in rocks and minerals by neutron activation analysis is described. Two methods are used for pre-separating and concentrating the trace gold in geological samples. one of the methods is that the samples are dissolved in aqua regia solution; activated carbon paper pulp filter is used for pre-separating and concentrating trace gold by dynamic adsorption method; then the activated carbon containing gold was ashed at 650 ∼ 700 deg c. The other method is that the samples are dissolved in aqua regia solution; the polyurethane foam plastic filled with activated carbon is used for pre-separating and concentrating trace gold by dynamic adsorption method; then the foam plastic containing gold was ashed at 650 deg c. The gold in ashes is determinated by neutron activation analysis. The detection limit is 0.004ng/g. The accuracy of the method is examined by gold in reference standard material. The results of this method are in good agreement with the recommended value. For analysis of the trace gold by the methods of instrumental neutron activation analysis and epithermal neutron activation analysis, the interference of 411.8 keV γ-ray from 153 Sm, 152 Eu and fission products of uranium and the correction methods are discussed

  12. A new facility for rapid neutron activation analysis

    International Nuclear Information System (INIS)

    Zeisler, R.; Makarewicz, M.; Grass, F.; Casta, J.

    1996-01-01

    Many research groups have undertaken efforts on the utilization of short-lived nuclides in a broad spectrum of neutron activation analysis (NAA) applications. The advantages of these approaches are obvious because the information on the sample can be extracted more rapidly. In addition to its other advantages, NAA can become extremely competitive in price and analysis time. Nevertheless, NAA with short-lived nuclides has not gained broad popularity, perhaps because of some difficulties in accuracy and the availability of suitable irradiation facilities. This report discusses the ASTRA reactor for neutron activation analysis capabilities

  13. 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

  14. Pretreatment procedures applied to samples to be analysed by neutron activation analysis at CDTN/CNEN

    International Nuclear Information System (INIS)

    Francisco, Dovenir; Menezes, Maria Angela de Barros Correia

    2009-01-01

    The neutron activation technique - using several methods - has been applied in 80% of the analytical demand of Division for Reactor and Analytical Techniques at CDTN/CNEN, Belo Horizonte, Minas Gerais. This scenario emphasizes the responsibility of the Laboratory to provide and assure the quality of the measurements. The first step to assure the results quality is the preparation of the samples. Therefore, this paper describes the experimental procedures adopted at CDTN/CNEN in order to uniform conditions of analysis and to avoid contaminations by elements present everywhere. Some of the procedures are based on methods described in the literature; others are based on many years of experience preparing samples from many kinds of matrices. The procedures described are related to geological material - soil, sediment, rock, gems, clay, archaeological ceramics and ore - biological materials - hair, fish, plants, food - water, etc. Analytical results in sediment samples are shown as n example pointing out the efficiency of the experimental procedure. (author)

  15. Cadmium determination in biological samples using neutron activation analysis with radiochemical separations

    International Nuclear Information System (INIS)

    Munoz A, Luis; Gras R, Nuri

    2005-01-01

    Chile has 7500 km of coastline on the Southern Pacific ocean,with about 4500 km of continental coastline that contains a variety of different geographical zones.This variety means that there is a great diversity of marine resources such as fish, shellfish and seaweeds. The utilization of these resources has been increasing in recent years making this sector an economically important one. The catch as of May 2002 came to 1.9 million tons and exports of the different species amounted to US$611.5 million as of April.But this important economic resource is being threatened by the technical demands imposed by importing countries, mainly the specific requirements for sanitary certification for fishery export products, depending on the markets of destination. The chemical element cadmium is one of the most strictly controlled elements due some shellfish accumulate a large amount of this element and to its high toxicity. The Chilean standard's analytical procedures for cadmium determination in hydro biological products, which must be met by laboratories that certify and control these products for export, are now being evaluated. Through its Chemical Metrology Unit, the Chilean Nuclear Energy Commission is strongly supporting this sector by preparing the secondary reference or control materials, and it has developed and implemented nuclear analytical methods for the certification of these materials, which will be used mostly in collaborative studies. This work describes the methodology developed for the determination of cadmium in biological samples, particularly in shellfish and fish. The method is based on neutron activation analysis with radiochemical separations, using the radioisotopes 115 Cd and 115m In, generated in the samples by bombarding with neutrons in a nuclear reactor. The samples were digested at 110 o C with H 2 SO 4 and H 2 O 2 and then the radioactive cadmium element was separated from the other elements present in the samples using a Bio Rad AG 2-X8

  16. DETERMINATION OF LIMIT DETECTION OF THE ELEMENTS N, P, K, Si, Al, Fe, Cu, Cd, WITH FAST NEUTRON ACTIVATION USING NEUTRON GENERATOR

    OpenAIRE

    Sunardi, Sunardi; Muryono, Muryono

    2010-01-01

    Determination of limit detection of the elements N, P, K, Si, Al, Fe, Cu, Cd, with fast neutron activation using neutron generator has been done.  Samples prepared from SRM 2704, N, P, K elements from MERCK, Cu, Cd, Al from activation foil made in San Carlos, weighted and packed for certain weight then iradiated during 30 minutes with 14 MeV fast neutron using the neutron generator and then counted with gamma spectrometry (accuspec).  At this research condition of neutron generator was set at...

  17. A comparative examination of several techniques for the routine determination of mercury in biological samples by neutron activation analysis

    International Nuclear Information System (INIS)

    Faanhof, A.; Das, H.A.

    1978-01-01

    A comparative examination of the most important techniques for the separation of mercury from irradiated biological material was made. Procedures for routine analysis and results for standard materials are given. Activation was performed at a thermal neutron flux of approximately 5x10 12 nxcm -2 xs -1 during ( 3 ) 2 offers a convenient solution to this problem. The variation of the neutron flux with the irradiation position can be measured by the application of thin iron rings as flux monitors. Losses of mercury due to uptake in the wall of the irradiation containers are negligible. The most powerful destruction technique for large samples is that based on a stainless-steel bomb. (T. I.)

  18. Educational activities for neutron sciences

    International Nuclear Information System (INIS)

    Hiraka, Haruhiro; Ohoyama, Kenji; Iwasa, Kazuaki

    2011-01-01

    Since now we have several world-leading neutron science facilities in Japan, enlightenment activities for introducing neutron sciences, for example, to young people is an indispensable issue. Hereafter, we will report present status of the activities based on collaborations between universities and neutron facilities. A few suggestions for future educational activity of JSNS are also shown. (author)

  19. Triton burnup measurements in KSTAR using a neutron activation system

    Energy Technology Data Exchange (ETDEWEB)

    Jo, Jungmin; Shi, Yue-Jiang; Chung, Kyoung-Jae, E-mail: jkjlsh1@snu.ac.k; Hwang, Y. S. [Department of Nuclear Engineering, Seoul National University, Seoul 151-744 (Korea, Republic of); Cheon, MunSeong; Rhee, T.; Kim, Junghee [National Fusion Research Institute, Daejeon 34133 (Korea, Republic of); Kim, Jun Young [Korea University of Science and Technology, Daejeon 34133 (Korea, Republic of); Isobe, M.; Ogawa, K. [National Institute for Fusion Science, Toki-shi (Japan); SOKENDAI (The Graduate University for Advanced Studies), Toki-shi (Japan)

    2016-11-15

    Measurements of the time-integrated triton burnup for deuterium plasma in Korea Superconducting Tokamak Advanced Research (KSTAR) have been performed following the simultaneous detection of the d-d and d-t neutrons. The d-d neutrons were measured using a {sup 3}He proportional counter, fission chamber, and activated indium sample, whereas the d-t neutrons were detected using activated silicon and copper samples. The triton burnup ratio from KSTAR discharges is found to be in the range 0.01%–0.50% depending on the plasma conditions. The measured burnup ratio is compared with the prompt loss fraction of tritons calculated with the Lorentz orbit code and the classical slowing-down time. The burnup ratio is found to increase as plasma current and classical slowing-down time increase.

  20. Neutron Activation analysis of waste water; Analisis de aguas residuales mediante activacion neutronica

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez H, V

    1997-12-01

    An instrumental neutron activation analysis for the simultaneous determination of chlorine, bromine, sodium, manganese, cobalt, copper, chromium, zinc, nickel, antimony and iron in waste water is described. They were determined in waste water samples under normal conditions by non-destructive neutron activation simultaneously using a suitable monostandard method. Standardized water samples were used and irradiated in polyethylene ampoules at a neutron flux of 10{sup 13} cm{sup -2} s{sup -1} for periods of 1 minute, 1 and 10 hours. A Ge hyperpure detector was used for your activity determination, with count times of 60, 180, 300 and 600 seconds. The obtained results show than the method can be utilized for the determination of this elements without realize anything previous treatment of the samples. (Author).

  1. An investigation of tungsten by neutron activation techniques

    International Nuclear Information System (INIS)

    Svetsreni, R.

    1978-01-01

    This investigation used neutron from Plutonium-Beryllium source (5 curie) to analyse the amount of tungsten in tungsten oxide which was extracted from tungsten ores, slag and tungsten alloy of tungsten iron and carbon. The technique of neutron activation analysis with NaI(Tl) gamma detector 3'' x 3'' and 1024 multichannel analyzer. The dilution technique was used by mixing Fe 2 O 3 or pure sand into the sample before irradiation. In this study self shielding effect in the analysis of tungsten was solved and the detection limit of the tungsten in the sample was about 0.5%

  2. Neutron activation measurements in research reactor concrete shield

    International Nuclear Information System (INIS)

    Zagar, T.; Ravnik, M.; Bozic, M.

    2001-01-01

    The results of activation measurement inside TRIGA research reactor concrete shielding are given. Samples made of ordinary and barytes concrete together with gold and nickel foils were irradiated in the reactor body. Long-lived neutron-induced gamma-ray-emitting radioactive nuclides in the samples were measured with HPGe detector. The most active longlived radioactive nuclides in ordinary concrete samples were found to be 60 Co and 152 Eu and in barytes concrete samples 60 Co, 152 Eu and 133 Ba. Measured activity density of all nuclides was found to decrease almost linearly with depth in logarithmic scale.(author)

  3. Isotope identification of Saudi Arabian rock samples from Umm Al-Birak using neutron activation analysis

    International Nuclear Information System (INIS)

    Kahtani, S.A.

    1984-12-01

    Forty eight geological samples from Umm Al-Birak area in the northwest part of Saudi Arabia are analyzed qualitatively and quantitatively using the instrumental neutron activation analysis technique. Samples are properly prepared and irridiated in the reactor facilities of the National Tsing-Hue University in Taiwan. Gamma spectra from high resolution detector are analyzed using BRUTAL code. Final calculations are made by two independent programs, namely, ELCAL and SMPCL. Twenty trace elements are identified and their concentrations are used in the investigation of the geochemistry of the Umm Al-Birak microgranite site. These elements are: Co, Cr, Eu, Fe, Hf, K, La, Lu, Na, Rb, Sc, Sm, Ta, Tb, Th, U, Yb, Zn and Zr. It is shown that high grade area is a differentiated rock that crystallized in a late stage of Umm Al-Birak microgranite area. 43 Ref

  4. Neutron spin precession in samples of polarised nuclei and neutron spin phase imaging

    Energy Technology Data Exchange (ETDEWEB)

    Piegsa, Florian Michael

    2009-07-09

    The doublet neutron-deuteron (nd) scattering length b{sub 2,d}, which is at present only known with an accuracy of 5%, is particularly well suited to fix three-body forces in novel effective field theories at low energies. The understanding of such few-nucleon systems is essential, e.g. for predictions of element abundances in the big-bang and stellar fusion. b{sub 2,d} can be obtained via a linear combination of the spin-independent nd scattering length b{sub c,d} and the spin-dependent one, b{sub i,d}. The aim of this thesis was to perform a high-accuracy measurement of the latter to improve the relative accuracy of b{sub 2,d} below 1%. The experiment was performed at the fundamental neutron physics beam line FUNSPIN at the Paul Scherrer Institute in Switzerland. It utilises the effect that the spin of a neutron passing through a target with polarised nuclei performs a pseudomagnetic precession proportional to the spin-dependent scattering length of the nuclei. An ideal method to measure this precession angle very accurately is Ramsey's atomic beam technique, adapted to neutrons. The most crucial part of the experimental setup is the so-called frozen spin target, which consists of a specially designed dilution refrigerator and contains a sample with dynamically polarised nuclear spins. The polarisation of the sample is determined by nuclear magnetic resonance (NMR) techniques. It turned out that the relaxation of the nuclear spins during the necessary ''cross-calibration'' of the two employed NMR systems is ultimately limiting the achievable accuracy of b{sub i,d}. During the extensive use of the Ramsey resonance method in the neutron-deuteron experiment, an idea emerged that the applied technique could be exploited in a completely different context, namely polarised neutron radiography. Hence, the second part of the thesis covers the development of a novel neutron radiography technique, based on the spin-dependent interaction of the

  5. Neutron spin precession in samples of polarised nuclei and neutron spin phase imaging

    International Nuclear Information System (INIS)

    Piegsa, Florian Michael

    2009-01-01

    The doublet neutron-deuteron (nd) scattering length b 2,d , which is at present only known with an accuracy of 5%, is particularly well suited to fix three-body forces in novel effective field theories at low energies. The understanding of such few-nucleon systems is essential, e.g. for predictions of element abundances in the big-bang and stellar fusion. b 2,d can be obtained via a linear combination of the spin-independent nd scattering length b c,d and the spin-dependent one, b i,d . The aim of this thesis was to perform a high-accuracy measurement of the latter to improve the relative accuracy of b 2,d below 1%. The experiment was performed at the fundamental neutron physics beam line FUNSPIN at the Paul Scherrer Institute in Switzerland. It utilises the effect that the spin of a neutron passing through a target with polarised nuclei performs a pseudomagnetic precession proportional to the spin-dependent scattering length of the nuclei. An ideal method to measure this precession angle very accurately is Ramsey's atomic beam technique, adapted to neutrons. The most crucial part of the experimental setup is the so-called frozen spin target, which consists of a specially designed dilution refrigerator and contains a sample with dynamically polarised nuclear spins. The polarisation of the sample is determined by nuclear magnetic resonance (NMR) techniques. It turned out that the relaxation of the nuclear spins during the necessary ''cross-calibration'' of the two employed NMR systems is ultimately limiting the achievable accuracy of b i,d . During the extensive use of the Ramsey resonance method in the neutron-deuteron experiment, an idea emerged that the applied technique could be exploited in a completely different context, namely polarised neutron radiography. Hence, the second part of the thesis covers the development of a novel neutron radiography technique, based on the spin-dependent interaction of the neutron with ferromagnetic samples and magnetic fields

  6. Precision of neutron activation analysis for environmental biological materials

    International Nuclear Information System (INIS)

    Hamaguchi, Hiroshi; Iwata, Shiro; Koyama, Mutsuo; Sasajima, Kazuhisa; Numata, Yuichi.

    1977-01-01

    Between 1973 and 1974 a special committee ''Research on the application of neutron activation analysis to the environmental samples'' had been organized at the Research Reactor Institute, Kyoto University. Eleven research groups composed mainly of the committee members cooperated in the intercomparison programme of the reactor neutron activation analysis of NBS standard reference material, 1571 Orchard Leaves and 1577 Bovine Liver. Five different type of reactors were used for the neutron irradiation; i.e. KUR reactor of the Research Reactor Institute, Kyoto University, TRIGA MARK II reactor of the Institute for Atomic Energy, Rikkyo University, and JRR-2, JRR-3, JRR-4 reactor of Japan Atomic Energy Research Institute. Analyses were performed mainly by instrumental method. Precision of the analysis of 23 elements in Orchard Leaves and 13 elements in Bovine Liver presented by the different research groups was shown in table 4 and 5, respectively. The coefficient of variation for these elements was from several to -- 30 percent. Averages given to these elements agreed well with the NBS certified or reference values. Thus, from the practical point of view for the routine multielement analysis of environmental samples, the validity of the instrumental neutron activation technique for this purpose has been proved. (auth.)

  7. Determination of rhenium in biological and environmental samples by radiochemical neutron activation analysis

    International Nuclear Information System (INIS)

    Kucera, J.; Mizera, J.; Randa, Z.; Byrne, A.R.; Lucanikova, M.

    2006-01-01

    Radiochemical neutron activation procedures using liquid-liquid extraction with tetraphenylarsonium chloride in chloroform from 1 M HCl and solid extraction with ALIQUAT 336 incorporated in a polyacrylonitrile binding matrix from 0.1 M HCl were developed for accurate determination of rhenium in biological and environmental samples at the sub-ng.g -1 level. Concentrations of Re in the range of 0.1 to 2.4 ng.g -1 were determined in several botanical reference materials (RM), while in a RM of road dust a value of approx. 10 ng.g -1 was found. Significantly elevated values of Re, up to 90 ng.g -1 , were found in seaweed (brown algae). Results for Re in the brown algae Fucus vesiculosus in which elevated 99 Tc values had previously been determined suggest possible competition between Re and Tc in the accumulation process. (author)

  8. Fast neutron activation analysis by means of low voltage neutron generator

    Directory of Open Access Journals (Sweden)

    M.E. Medhat

    Full Text Available A description of D-T neutron generator (NG is presented. This machine can be used for fast neutron activation analysis applied to determine some selected elements, especially light elements, in different materials. Procedure of neutron flux determination and efficiency calculation is described. Examples of testing some Egyptian natural cosmetics are given. Keywords: Neutron generator, Fast neutron activation analysis, Elemental analysis

  9. Recoil Reactions in Neutron-Activation Analysis. The Szilard-Chalmers Effect Applied in the Analysis of Biological Samples; II. Transfer of Activities from Container Material to Sample

    Energy Technology Data Exchange (ETDEWEB)

    Brune, D

    1965-01-15

    The present investigation consists of two parts. The one part concerns the application of the Szilard-Chalmers effect in the separation of activities from neutron-irradiated biological material. The nuclides As-76, Au-198, Br-82, Ca-47, Cd-115, Cl-38, Co-60, Cr-51, Cs-134, Cu-64, Fe-59, Mg-27, Mo-99, Na-24, P-32, Rb-86, Se-75 and Zn-65 were extracted from either liver tissue, whole blood or muscle tissue. The extractions were made in water, 0.1 N HCl, 1 N HCl or conc. HCl respectively. The nuclides belonging to the alkali metals together with Br and Cl, were found present in the water and hydrochloric extracts to 96 per cent or more. In the conc. HCl extracts, the greater part of the nuclides were recovered to 90 per cent or more. The enrichment of the different nuclides obtained in the Szilard-Chalmers process was investigated as follows. After extraction of the nuclides from the irradiated material the solution obtained was divided into two parts, one of which was reactivated. The specific activities of the nuclides in the two solutions were then compared, thus giving the enrichment factor In one case, the residue of organic material after extraction was reactivated and the activity compared to the initial one. The effect of dilution together with the application of short irradiation periods favouring higher yield was investigated in the separation of Fe-59 from whole blood samples irradiated in frozen conditions. The other part of the investigation concerns an estimation of the amounts of the activities originating from polyethylene and quartz containers transferred to container surface due to the recoil effect in the thermal neutron-capture process, thus causing contamination of the sample. The universal range-energy relationship given by Lindhard and Scharff has been applied in these calculations. As regards containers with impurities in the ppm region, the amounts of activities transferred owing to this effect were found to be quite negligible. However, when

  10. Study on neutron activation analysis

    International Nuclear Information System (INIS)

    Chung, Yong Sam; Cho, Seung Yeon

    1993-01-01

    Environmental samples were analyzed quantitatively by neutron activation analysis using high resolution γ-ray spectrometry. The accuracy and precision of the method were checked by the analysis of reference materials, Urban Particulate Matter (NBS SRM 1648) and Coalfly ash (NBS SRM 1633a). Airborne particulates collected for 6 months with low volume air sampler at the outer area of Seoul were analyzed as the start of full scale airborne particulates research. We analyzed 19 trace elements from the samples and the NAA method was confirmed to be utilized for environmental pollution research. (Author)

  11. Study the Possibility of measuring Heavy Metals Arising from Gold Mining Sample using 252Cf Neutron Source

    International Nuclear Information System (INIS)

    Soliman, N.F.

    2012-01-01

    Mining activities contribute immensely to trace element pollution .The present work studied the possibility of measuring heavy metals arising from gold mining areas Eastern Desert in Egypt using the isotopic 252 Cf neutron source. 38.5 g of the sample is irradiated in a neutron field of 252 Cf for 36.75 days and 0.3 mg of the sample is irradiated at the Pneumatic Irradiation Rabbit System (PIRS) built in the vertical thermal column of the ET-RR-2 reactor . The induced activities in the samples are measured using two high resolution f ray spectrometry systems (including two calibrated HPGe detectors). The kο standardization neutron activation analysis (kο-NAA) method was used to analyze the sample under investigation. Thermal to epithermal flux ratio fat the two irradiation positions are measured. The obtained results indicated that the values of the suspected heavy metals such as sodium, magnesium, potassium, manganese, arsenic, ruthenium and tantalum were higher than the background values, signifying accumulation of these heavy metals due to gold mining activities .The accuracy and precision of the method has been evaluated

  12. Elemental analysis of fertilizer by fast neutron activation

    International Nuclear Information System (INIS)

    Bodart, F.; Deconninck, G.

    1977-01-01

    A simple and accurate technique has been developed to analyse commercial fertilizers for phosphorus, potassium, chlorine, magnesium and silicon. The method is based on fast-neutron activation using a neutron flux of 2x10 11 neutrons/second. The optimum analytical conditions are tabulated. After irradiation, the sample is measured on a conventional counting system including a Ge(Li) detector (10% efficiency and 2 keV resolution for 60 Co) and a multichannel analyser. Monitor foils radioactivity are measured separately at the same time with a 2''x2''NaI detector coupled with a single channel analyser and a scaler. Fast neutron activation has proved to be a fast, simple, reliable and low cost analytical technique for the determination of phosphorus, silicon, potassium, magnesium and chlorine in fertilizers. Not less than five phosphorus determinations are possible in one hour, while two potassium, magnesium and chlorine determinations are made at the same time. (T.G.)

  13. Major and minor elements analysis in soil samples by neutron activation analysis and X-ray fluorescence

    International Nuclear Information System (INIS)

    Morcelli, Claudia Petronilho Ribeiro; Ana Maria Graciano; Enzweiler, Jacinta

    2002-01-01

    In the present work, Instrumental Neutron Activation Analysis (INAA) and X-Ray Fluorescence were employed to analyze major and minor elements in soil samples collected near Bandeirantes road. Elements of environmental interest, such as Al, Sb, As, Ba, Cd, Pb, Co, Cu, Cr, Fe, Mn, Mo, Ni, Se, V and Zn, which have reference background levels, were determined. The samples were dried in an oven at 40 deg C, were sieved (<2 mm), grinded and were analyzed by INAA and FRX. The aims of this work were: to evaluate the possible variations in the concentration levels in soil due to emission of particulate from vehicles and other anthropogenic sources; to compare the results obtained by using both techniques. This preliminary study showed that the concentration levels of the elements of environmental interest agree with reference values for tropical soils in the sampling sites, except for Ba, which presented higher values. (author)

  14. Study on the application of crown ether for neutron activation analysis of rubidium and rhenium in rock samples

    International Nuclear Information System (INIS)

    Wang Xiaolin; Fu Yibei; Liu Yinong; Xiong Zonghua; Hao Fanhua

    1996-01-01

    The extraction behaviour of rubidium and rhenium with 18-crown-6 (18C6) and benzo-15-crown-5 (B15C5) in nitrobenzene from picric acid or potassium hydroxide solution are studied and methods for separation and determination are developed. The molar ratio of 18C6 to Rb and B15C5 to Re in the extracted species is probably 2:1. Rubidium and rhenium in rock samples are satisfactorily determined by neutron activation method

  15. Procedures for multielement analysis using high-flux fast-neutron activation

    International Nuclear Information System (INIS)

    Williams, R.E.; Hopke, P.K.; Meyer, R.A.

    1981-06-01

    Improvements have been made in the rabbit system used for multi-element fast-neutron activation analysis at the Lawrence Livermore National Laboratory Rotating Target Neutron Source, RTNS-I. Procedures have been developed for the analysis of 20 to 25 elements in samples with an inorganic matrix and 10 to 15 elements in biological samples, without the need for prohibitively expensive, long irradiations. Results are presented for the analysis of fly ash, orchard leaves, and bovine liver

  16. Utilization of boron irradiation filters in reactor neutron activation via epithermal (n,γ) and fast neutron reactions

    International Nuclear Information System (INIS)

    Chisela, F.

    1986-01-01

    The technique of instrumental neutron activation analysis based on irradiation with reactor epithermal and fast neutrons has been described and evaluated. Important characteristics of boron neutron absorbers used to remove thermal neutrons from the reactor neutron spectrum have been examined and compared with those of cadmium. Three boron compound shields, have been designed and constructed at the BER II 5MW reactor for use in epithermal neutron activation analysis of biological materials. The major advantages offered by these filters in this application include the flexibility of varying the filter thickness, the low radioactivity induced in the filters during irradiation, ease of fabrication and the relatively low cost of the filter materials. The radiation heating due to the 10 B(n,α) 7 Li-reaction has been experimentally investigated for the filters used and the results obtained confirm the necessity for efficient cooling of these filters during irradiation. Three irradiation facilities have been characterized with respect to the neutron flux density and the flux spatial distribution. An experiment has been designed and carried out to compensate the flux inhomogeneity in two irradiation positions of the DBV facility caused by the reactor geometry. Several biological samples including well characterized reference materials have been analysed after epithermal activation and the results compared with those obtained with the classical thermal neutron activation method. Improved sensitivity of determination has been found for elements with high resonance integral to thermal neutron cross section ratios (RI/σ 0 ). The range of elements that can be determined instrumentally is extended and the time scale of analysis is considerably reduced. (orig.) [de

  17. Comparison of instrumental neutron activation analysis and instrumental charged-particle activation analysis for determining of Zn-68 abundance

    International Nuclear Information System (INIS)

    Rafii, H.; Mirzaei, M.; Aslani, G.R.; Kamali-Dehghan, M.; Rajamand, A-A.; Rahiminejad, A.; Mirzajani, N.; Sardari, D.; Shahabi, I.; Majidi, F.

    2004-01-01

    Gallium-67 has found important applications in nuclear medicine since last decades. The bombardment of enriched zinc-68 by proton beams in cyclotron is the most suitable method for the carrier-free production of this radionuclide. Any traces and isotopic impurities of the target cause serious radiological hazards because of their associated induced radioactivities. Trace analysis and Zn-68 content determination of the target material before any bombardment and chemical separation provide a valuable assessment of desired product. The elemental abundance evaluation of enriched isotopes is generally carried out by inductively coupled plasma-mass spectrometry method, ICP-Ms Instrumental neutron activation analysis and instrumental charged particle activation analysis. International neutron activation analysis and instrumental charged- particle activation analysis, looks be an alternative nuclear method for determining the abundance evaluation of enriched Zn-68 enrichment in two different samples has been studied by mean of international neutron activation analysis and instrumental charged- particle activation analysis . One sample was purchased from a French company, cortecnet, and the other was separated by an electromagnetic system in the Ions source department of our center, NRCAM. The neutron or proton irradiation was took place respectively in miniature neutron source reactor of Esfahan by flux of (1 to 5) 10 11 n/cm 2 .sec for 30 min and in Cyclon30 by 19 MeV proton beams of 100μA current for 12 min. The produced radioactivity was measured by HpGe detector for determination of trace impurities and evaluation of Zn-68 content in the samples. The result shows a good agreement with the reported ones by their producers and their low derivation of about ± indicates that the international neutron activation analysis and instrumental charged- particle activation analysis are relatively precise and rapid and each one can be used as a supplemental method for analyzing

  18. Neutron activation analysis of high purity substances

    International Nuclear Information System (INIS)

    Gil'bert, Eh.N.

    1987-01-01

    Peculiarities of neutron-activation analysis (NAA) of high purity substances are considered. Simultaneous determination of a wide series of elements, high sensitivity (the lower bound of determined contents 10 -9 -10 -10 %), high selectivity and accuracy (Sr=0.10-0.15, and may be decreased up to 0.001), possibility of analysis of the samples from several micrograms to hundreds of grams, simplicity of calibration may be thought NAA advantages. Questions of accounting of NAA systematic errors associated with the neutron flux screening by the analysed matrix and with production of radionuclides of determined elements from accompanying elements according to concurrent nuclear reactions, as well as accounting of errors due to self-absorption of recorded radiation by compact samples, are considered

  19. Simulation and preliminary experimental results for an active neutron counter using a neutron generator for a fissile material accounting

    International Nuclear Information System (INIS)

    Ahn, Seong-Kyu; Lee, Tae-Hoon; Shin, Hee-Sung; Kim, Ho-Dong

    2009-01-01

    An active neutron coincidence counter using a neutron generator as an interrogation source has been suggested. Because of the high energy of the interrogation neutron source, 2.5 MeV, the induced fission rate is strongly affected by the moderator design. MCNPX simulation has been performed to evaluate the performance achieved with these moderators. The side- and bottom-moderator are significantly important to thermalize neutrons to induce fission. Based on the simulation results, the moderators are designed to be adapted to the experimental system. Their preliminary performance has been tested by using natural uranium oxide powder samples. For a sample of up to 3.5 kg, which contains 21.7 g of 235 U, 2.64 cps/g- 235 U coincidence events have been measured. Mean background error was 9.57 cps and the resultant coincidence error was 13.8 cps. The experimental result shows the current status of an active counting using a neutron generator which still has some challenges to overcome. However, the controllability of an interrogation source makes this system more applicable for a variety of combinations with other non-destructive methods like a passive coincidence counting especially under a harsh environment such as a hot cell. More precise experimental setup and tests with higher enriched samples will be followed to develop a system to apply it to an active measurement for the safeguards of a spent fuel treatment process.

  20. Determination of concentrations of chromium and other elements in soil and plant samples from leather tanning area by Instrumental Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Rohit Kumar; Rai, A.K.; Alamelu, D.; Acharya, R.

    2014-01-01

    Chromium, one of the toxic elements, along with other elements has been determined in samples of soil and plant (leaves and seeds) from Jajmau Area, Kanpur district, India, which is irrigated with effluent waste water from leather tanning industries. Soil and plant samples were collected from these areas and analyzed by Instrumental Neutron Activation Analysis (INAA) using high flux reactor neutrons and high resolution gamma-ray spectrometry. Concentrations of fifteen elements in soil and five elements in plant samples were determined by relative method. Chromium concentrations were found to be in range of 45-3,900 mg kg -1 in soil samples and 14-83 mg kg -1 in plant samples. This study showed that Cr is present in significant amounts, in the soil as well as in the plant samples, near to the leather tanning area. As a part of quality control work, IAEA reference material (RM) SL-3 and NIST standard reference material (SRM) 1645 were analyzed and the quality of the results has been evaluated by calculating % deviations from recommended/literature/certified values. (author)

  1. Investigations on the comparator technique used in epithermal neutron activation analysis

    International Nuclear Information System (INIS)

    Bereznai, T.; Bodizs, D.; Keoemley, G.

    1977-01-01

    The possible extension of the comparator technique of reactor neutron activation analysis into the field of epithermal neutron activation has been investigated. Ruthenium was used for multi-isotopic comparator. Experiments show that conversion of the so-called reference k-factors - determined by irradiation with reactor neutrons - into ksup(epi)-factors usable at activation under cadmium filter, can be evaluated with fair accuracy. Sources and extent of errors and their contribution to the final error of analysis are discussed. For equal irradiation and counting times advantage of ENAA for several elements is obvious: the much lower background activity permitted the sample to be measured closer to the detector, under better geometry conditions, consequently, permitting several elements to be determined quantitatively. The number of elements determined and the sensitivity of the method are much dependent on the experimental conditions, especially on the composition of the sample, on the PHIsub(e) value, the irradiation time and the efficiency of the Ge(Li) detector. (T.G.)

  2. Dynamically polarized samples for neutron protein crystallography at the Spallation Neutron Source

    International Nuclear Information System (INIS)

    Zhao, Jinkui; Pierce, Josh; Robertson, J. L.; Herwig, Kenneth W.; Myles, Dean; Cuneo, Matt; Li, Le; Meilleur, Flora; Standaert, Bob

    2016-01-01

    To prepare for the next generation neutron scattering instruments for the planned second target station at the Spallation Neutron Source (SNS) and to broaden the scientific impact of neutron protein crystallography at the Oak Ridge National Laboratory, we have recently ramped up our efforts to develop a dynamically polarized target for neutron protein crystallography at the SNS. Proteins contain a large amount of hydrogen which contributes to incoherent diffraction background and limits the sensitivity of neutron protein crystallography. This incoherent background can be suppressed by using polarized neutron diffraction, which in the same time also improves the coherent diffraction signal. Our plan is to develop a custom Dynamic Nuclear Polarization (DNP) setup tailored to neutron protein diffraction instruments. Protein crystals will be polarized at a magnetic field of 5 T and temperatures of below 1 K. After the dynamic polarization process, the sample will be brought to a frozen-spin mode in a 0.5 T holding field and at temperatures below 100 mK. In a parallel effort, we are also investigating various ways of incorporating polarization agents needed for DNP, such as site specific spin labels, into protein crystals. (paper)

  3. Epithermal neutron activation analysis of food

    International Nuclear Information System (INIS)

    Zikovsky, L.; Soliman, K.

    1999-01-01

    Food samples were irradiated with thermal and epithermal neutrons. The average ratios of thermal to epithermal activity were determined for 80 Br, 49 Ca, 38 Cl, 60m Co, 42 K, 27 Mg, 56 Mn, 24 Na, and 86m Rb. They were equal to 2.1, 26, 24, 6.6, 19, 16, 11, 23 and 1.9, respectively. Then, 57 food samples were analyzed by epithermal neutron activation analysis for Br and Rb. The concentrations (in ppm) of Br and Rb were in asparagus (2) 2.3, 11.5; beets (3) 0.5, 0.8; beef (3) 1.7, 3.6; cabbage (5) 0.5, 10.8; carrot (3) 0.2, 3.7; chicken (3) 0.6, 4.4; chocolate (7) 11.1, 18.7; egg (3) 0.9, 1.9; french bean (3) 0.3, 1.0; goose (2) 1.3, 9.3; lettuce (2) 0.9, 1.7; pork (1) 1.5, 4.4; potato (7) 1.0, 1.2; sausage (3) 4.8, 3.5; spinach (3) 3.6, 4.0; strawberry jam (3) 0.4, 1.4; tomato (1) 13.5, 14.6; turkey (3) 1.2, 4.9. respectively. The number of samples and analyzed is indicated in parentheses. (author)

  4. Designing on-line analyzer for coal on belt conveyor using neutron activation technique

    International Nuclear Information System (INIS)

    Rony Djokorayono; Agus Cahyono

    2014-01-01

    Basic design of on-line analyzer for coal on belt conveyor using neutron activation technique has been carried out. Compared with sampling technique, this neutron activation technique has some advantages in term of analysis accuracy and time. The design activities performed include the establishment of design requirements, functional requirements, technical requirements, technical specification, detection sub-system design, data acquisition subsystem design, and operator computer console design. This program will use Nal(Tl) scintillation detector to detect gamma-rays emitted by elements in coal due to neutron activation of a neutron source, "2"5"2Cf (Californium-252). This basic design of on-line analyzer for coal on belt conveyor using neutron activation technique should be followed up with the development of detailed design, prototype construction, and field testing. (author)

  5. Gamma-ray-spectroscopy following high-flux 14-MeV neutron activation

    International Nuclear Information System (INIS)

    Williams, R.E.

    1981-01-01

    The Rotating Target Neutron Source (RTNS-I), a high-intensity source of 14-MeV neutrons at the Lawrence Livermore National Laboratory (LLNL), has been used for applications in activation analysis, inertial-confinement-fusion diagnostic development, and fission decay-heat studies. The fast-neutron flux from the RTNS-I is at least 50 times the maximum fluxes available from typical neutron generators, making these applications possible. Facilities and procedures necessary for gamma-ray spectroscopy of samples irradiated at the RTNS-I were developed

  6. Gamma-ray-spectroscopy following high-flux 14-MeV neutron activation

    Energy Technology Data Exchange (ETDEWEB)

    Williams, R.E.

    1981-10-12

    The Rotating Target Neutron Source (RTNS-I), a high-intensity source of 14-MeV neutrons at the Lawrence Livermore National Laboratory (LLNL), has been used for applications in activation analysis, inertial-confinement-fusion diagnostic development, and fission decay-heat studies. The fast-neutron flux from the RTNS-I is at least 50 times the maximum fluxes available from typical neutron generators, making these applications possible. Facilities and procedures necessary for gamma-ray spectroscopy of samples irradiated at the RTNS-I were developed.

  7. Investigation of two slag samples using k0 neutron activation analysis through different standardization methods

    Directory of Open Access Journals (Sweden)

    M. Abd El-Samad

    2010-12-01

    Full Text Available Instrumental neutron activation analysis was used to determine concentrations of several major and trace elements in two slag samples. One slag supplied by one of Steel factory and the other one by an Aluminum factory of Egypt. The aim of the present work is to study the accuracy and precision of Internal Comparator k0 and external comparator k0 methods in industrial application. The two slag samples together with an international reference material Soil-7 and two thin gold foils samples (one bare and the other covered with cadmium were irradiated at the core of the Second Research Egyptian Reactor ET-RR-2 of about 13x10 13n/(cm s. The elemental concentration of 46Sc, 51Cr, 60Co, 65Zn, 74As, 82Br, 85Sr, 86Zr, 110mAg, 122Sb, 134Cs, 131Ba, 140La, 141Ce, 147Nd, 153Sm, 152Eu, 153Gd, 166Ho, 169Yb, 175Hf, 182Ta, 198Au and 233Pa (232Th-series were calculated.

  8. Multielement analysis of archaic Chinese bronze and antique coins by fast neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Tian, Y.H. (Academia Sinica, Lanzhou, Gansu (China). Inst. of Modern Physics); Pepelnik, R.; Fanger, H.U. (GKSS-Forschungszentrum Geesthacht GmbH, Geesthacht-Tesperhude (Germany, F.R.). Inst. fuer Physik)

    1990-01-01

    Samples of archaic bronze have been investigated by fast neutron activation analysis using both the absolute and relative method. The components Cu, Zn, Sn and Pb have been determined quantitatively. For the detection of lead via the short-lived isomeric state {sup 207m}Pb, cyclic activation and measurement technique was used with pneumatic sample transfer between detector and central irradiation position of the neutron tube. For non-destructive analysis of antique Chinese coins the samples had to be irradiated outside the neutron generator KORONA. The activation reactions, the evaluation of the elemental concentrations and the accuracy of the results are discussed. The data were corrected for {gamma}-ray self-absorption in the samples and summing of coincident {gamma}-rays in the detector. According to reported typical compositions of Chinese bronze from different dynasties, the age of the samples has been derived from the results obtained. (orig.).

  9. The effect of albedo neutrons on the neutron multiplication of small plutonium oxide samples in a PNCC chamber

    CERN Document Server

    Bourva, L C A; Weaver, D R

    2002-01-01

    This paper describes how to evaluate the effect of neutrons reflected from parts of a passive neutron coincidence chamber on the neutron leakage self-multiplication, M sub L , of a fissile sample. It is shown that albedo neutrons contribute, in the case of small plutonium bearing samples, to a significant part of M sub L , and that their effect has to be taken into account in the relationship between the measured coincidence count rates and the sup 2 sup 4 sup 0 Pu effective mass of the sample. A simple one-interaction model has been used to write the balance of neutron gains and losses in the material when exposed to the re-entrant neutron flux. The energy and intensity profiles of the re-entrant flux have been parameterised using Monte Carlo MCNP sup T sup M calculations. This technique has been implemented for the On Site Laboratory neutron/gamma counter within the existing MEPL 1.0 code for the determination of the neutron leakage self-multiplication. Benchmark tests of the resulting MEPL 2.0 code with MC...

  10. 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)

  11. Neutron activation analysis technique and X-ray fluorescence in bovine liver sample

    International Nuclear Information System (INIS)

    Maihara, V.A.; Favaro, D.I.T.; Vasconcellos, M.B.A.; Sato, I.M.; Salvador, V.L.

    2002-01-01

    Many analytical techniques have been used in food and diet analysis in order to determine a great number of nutritional elements, ranging from percentage to ng g -1 , with high sensitivity and accuracy. Instrumental Neutron activation Analysis (INAA) has been employed to certificate many trace elements in biological reference materials. More recently, the X-Ray Fluorescence (FRX-WD) has been also used to determine some essential elements in food samples. The INAA has been applied in nutrition studies in our laboratory at IPEN since the 80 s. For the development of analytical methodologies the use of the reference materials with the same characteristics of the sample analyzed is essential. Several Brazilian laboratories do not have conditions to use these materials due their high cost.In this paper preliminary results of commercial bovine liver sample analyses obtained by INAA and WD-XRF methods are presented. This sample was prepared to be a Brazilian candidate of reference material for a group of laboratories participating in a research project sponsored by FAPESP. The concentrations of some elements like Cl, K, Na, P, S and trace elements Br, Ca, Co, Cu, Fe, Mg, Mn, Mo, Rb, Se and Zn were determined by INAA and WD-XFR. For validation methodology of both techniques, NIST SRM 1577b Bovine Liver reference material was analyzed and the detection limits were calculated. The concentrations of elements determined by both analytical techniques were compared by using the Student's t-test and for Cl, Cu, Fe, K, Mg, Na, Rn and Zn the results do show no statistical difference for 95% significance level. (author)

  12. Current status of neutron activation analysis in HANARO Research Reactor

    International Nuclear Information System (INIS)

    Chung, Yong Sam; Moon, Jong Hwa; Sohn, Jae Min

    2003-01-01

    The facilities for neutron activation analysis in the HANARO (Hi-flux Advanced Neutron Application Research Reactor) are described and the main applications of NAA (Neutron Activation Analysis) are reviewed. The sample irradiation tube, automatic and manual pneumatic transfer system were installed at three irradiation holes of HANARO at the end of 1995. The performance of the NAA facility was examined to identify the characteristics of the tube transfer system, irradiation sites and custom-made polyethylene irradiation capsule. The available thermal neutron fluxes at irradiation sites are in the range of 3 x 10 13 - 1 x 10 14 n/cm 2 ·s and cadmium ratios are in 15 - 250. For an automatic sample changer for gamma-ray counting, a domestic product was designed and manufactured. An integrated computer program (Labview) to analyse the content was developed. In 2001, PGNAA (Prompt Gamma Neutron Activation Analysis) facility has been installed using a diffracted neutron beam of ST1. NAA has been applied in the trace component analysis of nuclear, geological, biological, environmental and high purity materials, and various polymers for research and development. The improvement of analytical procedures and establishment of an analytical quality control and assurance system were studied. Applied research and development for the environment, industry and human health by NAA and its standardization were carried out. For the application of the KOLAS (Korea Laboratory Accreditation Scheme), evaluation of measurement uncertainty and proficiency testing of reference materials were performed. Also to verify the reliability and to validate analytical results, intercomparison studies between laboratories were carried out. (author)

  13. Current status of neutron activation analysis in HANARO Research Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Chung, Yong Sam; Moon, Jong Hwa; Sohn, Jae Min [Korea Atomic Energy Research Institute, Daejeon (Korea)

    2003-03-01

    The facilities for neutron activation analysis in the HANARO (Hi-flux Advanced Neutron Application Research Reactor) are described and the main applications of NAA (Neutron Activation Analysis) are reviewed. The sample irradiation tube, automatic and manual pneumatic transfer system were installed at three irradiation holes of HANARO at the end of 1995. The performance of the NAA facility was examined to identify the characteristics of the tube transfer system, irradiation sites and custom-made polyethylene irradiation capsule. The available thermal neutron fluxes at irradiation sites are in the range of 3 x 10{sup 13} - 1 x 10{sup 14} n/cm{sup 2}{center_dot}s and cadmium ratios are in 15 - 250. For an automatic sample changer for gamma-ray counting, a domestic product was designed and manufactured. An integrated computer program (Labview) to analyse the content was developed. In 2001, PGNAA (Prompt Gamma Neutron Activation Analysis) facility has been installed using a diffracted neutron beam of ST1. NAA has been applied in the trace component analysis of nuclear, geological, biological, environmental and high purity materials, and various polymers for research and development. The improvement of analytical procedures and establishment of an analytical quality control and assurance system were studied. Applied research and development for the environment, industry and human health by NAA and its standardization were carried out. For the application of the KOLAS (Korea Laboratory Accreditation Scheme), evaluation of measurement uncertainty and proficiency testing of reference materials were performed. Also to verify the reliability and to validate analytical results, intercomparison studies between laboratories were carried out. (author)

  14. Applications of neutron activation analysis in environmental science, biology and geoscience

    International Nuclear Information System (INIS)

    1992-01-01

    The applications of neutron activation analysis technique with high sensitivity, good accuracy, multielemental analysis and non-destruction of samples in hydrosphere, soil and lithosphere, atmosphere, cosmosphere and biosphere were introduced in this book. A large amount of research activities in this field during the 20 years and more carried out by Neutron Activation Analysis Laboratory, Institute of High Energy Physics, Academia Sinica, was summarized. A number of the data and information with important scientific significance was provided

  15. Neutron Activation Analysis of Archaeological Pottery Samples of Large Size, Including Pieces of Low Symmetry Shape: How to Get Accurate Analytical Results in a Practical Way

    International Nuclear Information System (INIS)

    Bedregal, P.S.; Montoya, E.H.; Mendoza, P.; Ubillús, M.; Baltuano, O.; Hernández, Y.; Gago, J.; Cohen, I.M.

    2018-01-01

    The feasibility of the instrumental neutron activation analysis of entire pieces of archaeological pottery, using low thermal neutron fluxes, is examined and a new approach for the non-destructive analysis of entire pottery objects by INAA, using the conventional relative method, is described. The proposed method relies in the preparation of a comparison standard, which is a nominally identical replicate of the original object to be studied. INAA of small samples taken from that replicate allows determining its composition for the elements to be analyzed. Then the intact sample and intact standard are irradiated together with the neutrons from a nuclear reactor neutron beam, using a suitable turntable facility and monitored by neutron flux monitors. Finally, after proper decay times, the induced activities in sample, standard and flux monitors, are successively measured, by high-resolution gamma spectroscopy, using a high-efficiency germanium detector. In this way, several complicating effects such geometrical efficiency, neutron self-shielding and gamma ray attenuation are avoided and the need of complicated mathematical corrections is not needed. A potential advantage of the method is that it can be fully validated. Quantitative experiments using 7 - 13 hours of irradiation of pairs of 750 grams replicates, at low neutron fluxes of 3.9 x10 6 n cm -2 s -1 , followed by 100000 to 200000 seconds of counting in front of a 70% relative efficiency HPGe detector, led to recoveries between 90% and 110% for Sc and La. Another experiment, using pairs of replicates of small solid mud anthropomorphic objects, (weighing about 100 grams each), irradiated by 8 hours at a neutron flux of 10 9 n cm -2 s -1 , led to recoveries better than 90% and 110% for As, Ba, Ce, Co, Cr, Cs, Eu, Fe, Hf, La, Lu, Rb, Sb, Sc, Sm, Ta, Tb, Th, Yb and U, showing that the proposed method is suitable for LSNAA of entire pottery or mud archaeological objects. (author)

  16. Elemental analysis in bed sediment samples of Karnafuli estuarine zone in the Bay of Bengal by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Molla, N.I.; Hossain, S.M.; Basunia, S.; Miah, R.U.; Rahman, M.; Sikder, D.H.; Chowdhury, M.I.

    1997-01-01

    The concentration of rare earths and other elements have been determined in the bed sediment samples of Karnafuli estuarine zone in the Bay of Bengal by instrumental neutron activation analysis (INAA). The samples and the standards soil-5, soil-7, coal fly ash and pond sediment were prepared and simultaneously irradiated for short and long time at the TRIGA Mark-II research reactor facility of Atomic Energy Research Establishment, Savar, Dhaka. The maximum thermal neutron flux was of the order of 10 13 n x cm -2 x s -1 . After irradiation the radioactivity of the product nuclides was measured by using a high resolution high purity germanium detector system. Analysis of γ-ray spectra and quantitative analysis of the elemental concentration were done via the software GANAAS. It has been possible to determine the concentration level of 27 elements including the rare earths La, Ce, Sm, Eu, Tb, Dy and Yb and uranium and thorium. (author)

  17. Neutron activation spectrometry and neutron activation analysis in analytical geochemistry

    International Nuclear Information System (INIS)

    Dulski, P.; Moeller, P.

    1975-07-01

    The present report is to show the geochemists who are interested in neutron activation spectrometry (NAS) and neutron activation analysis (NAA) which analytical possibilities these methods offer him. As a review of these analytical possibilities, a lieterature compolation is given which is subdivided into two groups: 1) rock (basic, intermediary, acid, sediments, soils and nuds, diverse minerals, tectites, meteorites and lunar material). 2) ore (Al, Au, Be, Cr, Cu, Mn, Mo, Fe, Pb, Pt, Sn, Ti, W, Zn, Zr, U and phosphate ore, polymetallic ores, fluorite, monazite and diverse ores). The applied methods as well as the determinable elements in the given materials can be got from the tables. On the whole, the literature evaluation carried out makes it clear that neutron activation spectrometry is a very useful multi-element method for the analysis of rocks. The analysis of ores, however, is subjected to great limitations. As rock analysis is very frequently of importance in prospecting for ore deposits, the NAS proves to be extremely useful for this very field of application. (orig./LH) [de

  18. Aspects of precision and accuracy in neutron activation analysis

    International Nuclear Information System (INIS)

    Heydorn, K.

    1980-03-01

    Analytical results without systematic errors and with accurately known random errors are normally distributed around their true values. Such results may be produced by means of neutron activation analysis both with and without radiochemical separation. When all sources of random variation are known a priori, their effect may be combined with the Poisson statistics characteristic of the counting process, and the standard deviation of a single analytical result may be estimated. The various steps of a complete neutron activation analytical procedure are therefore studied in detail with respect to determining their contribution to the overall variability of the final result. Verification of the estimated standard deviation is carried out by demonstrating the absence of significant unknown random errors through analysing, in replicate, samples covering the range of concentrations and matrices anticipated in actual use. Agreement between the estimated and the observed variability of replicate results is then tested by a simple statistic T based on the chi-square distribution. It is found that results from neutron activation analysis on biological samples can be brought into statistical control. In routine application of methods in statistical control the same statistical test may be used for quality control when some of the actual samples are analysed in duplicate. This analysis of precision serves to detect unknown or unexpected sources of variation of the analytical results, and both random and systematic errors have been discovered in practical trace element investigations in different areas of research. Particularly, at the ultratrace level of concentration where there are few or no standard reference materials for ascertaining the accuracy of results, the proposed quality control based on the analysis of precision combined with neutron activation analysis with radiochemical separation, with an a priori precision independent of the level of concentration, becomes a

  19. Manual for the Portable Handheld Neutron Counter (PHNC) for Neutron Survey and the Measurement of Plutonium Samples

    International Nuclear Information System (INIS)

    Menlove, H.O.

    2005-01-01

    We have designed a portable neutron detector for passive neutron scanning measurement and coincidence counting of bulk samples of plutonium. The counter will be used for neutron survey applications as well as the measurement of plutonium samples for portable applications. The detector uses advanced design 3 He tubes to increase the efficiency and battery operated shift register electronics. This report describes the hardware, performance, and calibration for the system

  20. Neutron fluence spectrometry using disk activation

    International Nuclear Information System (INIS)

    Loevestam, Goeran; Hult, Mikael; Fessler, Andreas; Gasparro, Joel; Kockerols, Pierre; Okkinga, Klaas; Tagziria, Hamid; Vanhavere, Filip; Wieslander, J.S. Elisabeth

    2009-01-01

    A simple and robust detector for spectrometry of environmental neutrons has been developed. The technique is based on neutron activation of a series of different metal disks followed by low-level gamma-ray spectrometry of the activated disks and subsequent neutron spectrum unfolding. The technique is similar to foil activation but here the applied neutron fluence rates are much lower than usually in the case of foil activation. The detector has been tested in quasi mono-energetic neutron fields with fluence rates in the order of 1000-10000 cm -2 s -1 , where the obtained spectra showed good agreement with spectra measured using a Bonner sphere spectrometer. The detector has also been tested using an AmBe source and at a neutron fluence rate of about 40 cm -2 s -1 , again, a good agreement with the assumed spectrum was achieved

  1. Neutron activation analysis: recent developments and applications

    International Nuclear Information System (INIS)

    Acharya, R.; Reddy, A.V.R.

    2012-01-01

    Neutron activation analysis (NAA) is a powerful isotope specific nuclear analytical technique for simultaneous determination of major to trace elemental concentrations in diverse matrices. NAA is associated with high analytical sensitivities and low detection limits (ppm to ppb) due to utilization of high neutron flux from research reactors and high efficiency high resolution gamma ray spectrometry. Elemental concentrations are determined either by conventional NAA using relative method or by single comparator method of NAA (k 0 -NAA). Since 1994, Radiochemistry Division is actively engaged in developments and applications of k 0 -based NAA and Prompt Gamma ray NAA (PGNAA) methods for compositional characterization of materials, in addition to conventional instrumental NAA (INAA) and chemical NAA (CNAA) methods for total as well as speciation studies. The article briefly summarizes developments of k 0 based method of NAA using an external single comparator (k 0 -NAA) and an internal monostandard (lM-NAA) and PGNAA and their applications to small as well as large size samples. The article also briefly highlights the application of INAA and chemical NAA (CNAA) for speciation studies of arsenic and iodine in environmental and food samples respectively and bioaccesibility of selenium in food samples and trace elements wheatgrass samples

  2. Identification of cadmium in biological samples using neutron activation analysis with radiochemistry separations

    International Nuclear Information System (INIS)

    Munoz A, Luis; Gras R, Nuri

    2002-01-01

    Chile's 7500 km coastline of the Southern Pacific ocean, with about 4500 km of continental coastline that contains a variety of different geographical zones. This variety means that there is a great diversity of marine resources such as fish, shellfish and seaweeds. The utilization of these resources has been increasing in recent years making this sector an economically important one. The catch as of May 2002 came to 1.9 million tons and exports of the different species amounted to US$611.5 million as of April. But this important economic resource is being threatened by the technical demands imposed by importing countries, mainly the specific requirements for sanitary certification for fishery export products, depending on the markets of destination. The chemical element cadmium is one of the most strictly controlled elements due some shellfish accumulate a large amount of this element and to its high toxicity. The Chilean standard's analytical procedures for cadmium determination in hydro biological products, which must be met by laboratories that certify and control these products for export, are now being evaluated. Through its Chemical Metrology Unit, the Chilean Nuclear Energy Commission is strongly supporting this sector by preparing the secondary reference or control materials, and it has developed and implemented nuclear analytical methods for the certification of these materials, which will be used mostly in collaborative studies. This work describes the methodology developed for the determination of cadmium in biological samples, particularly in shellfish and fish. The method is based on neutron activation analysis with radiochemical separations, using the radioisotopes 115 Cd and 115m In, generated in the samples by bombarding with neutrons in a nuclear reactor. The samples were digested at 110 o C with H 2 SO 4 and H 2 O 2 and then the radioactive cadmium element was separated from the other elements present in the samples using a Bio Rad AG 2-X8 resin

  3. Factors affecting neutron measurements and calculations. Part C. Trace element concentrations in granite and their impact on thermal neutron activation

    International Nuclear Information System (INIS)

    Ruehm, Werner; Huber, Thomas; Nolte, Eckehart; Kato, Kazuo; Imanaka, Tetsuji; Egbert, Stephen D.

    2005-01-01

    Trace elements such as Li, B, Sm, and Gd can, despite their low elemental concentration in mineral materials, influence thermal neutron activation in Hiroshima and Nagasaki samples, due to their high thermal neutron absorption cross sections. This was demonstrated for a granite core, where the addition of those trace elements to the elemental composition of granite reduces the production of 152 Eu by some 25% at a depth of 25 cm from the surface. If typical concentrations of those trace elements are added to DS02 reference soil, however, the production of 152 Eu one meter above ground is not changed significantly, because of the high water content of the soil. This indicates that DS02 soil represents a reasonable reference material for the air-over-ground transport calculations. It must be kept in mind, however, that the local environment of any sample investigated for thermal neutron activation might be characterized by other elemental compositions. In particular, trace element and hydrogen concentrations could be considerably different from those used for DS02 reference soil. As an example it was demonstrated that in a granite gravestone thermal neutron activation of 36 Cl close to the surface might be, in the worst case, reduced by some 30%, due to increased local granite concentration in this type of environment. Beside other parameters such as, for example, individual sample geometry, the variability of trace elements in soil might be one reason for the variability that is observed in the individual thermal neutron activation measurements (Gold 1995). It is necessary, therefore, to carefully model the exposure geometry of the exposed material, its chemical composition, and the surrounding interface materials in order to obtain the best possible agreement in comparisons between calculated and measured data for thermal neutrons. (author)

  4. Isotopic neutron sources for neutron activation analysis

    International Nuclear Information System (INIS)

    Hoste, J.

    1988-06-01

    This User's Manual is an attempt to provide for teaching and training purposes, a series of well thought out demonstrative experiments in neutron activation analysis based on the utilization of an isotopic neutron source. In some cases, these ideas can be applied to solve practical analytical problems. 19 refs, figs and tabs

  5. Obsidian sources characterized by neutron-activation analysis.

    Science.gov (United States)

    Gordus, A A; Wright, G A; Griffin, J B

    1968-07-26

    Concentrations of elements such as manganese, scandium, lanthanum, rubidium, samarium, barium, and zirconium in obsidian samples from different flows show ranges of 1000 percent or more, whereas the variation in element content in obsidian samples from a single flow appears to be less than 40 percent. Neutron-activation analysis of these elements, as well as of sodium and iron, provides a means of identifying the geologic source of an archeological artifact of obsidian.

  6. Neutron fluence spectrometry using disk activation

    Energy Technology Data Exchange (ETDEWEB)

    Loevestam, Goeran [EC-JRC-Institute for Reference Materials and Measurements (IRMM), Retieseweg 111, B-2440 Geel (Belgium)], E-mail: goeran.loevestam@ec.europa.eu; Hult, Mikael; Fessler, Andreas; Gasparro, Joel; Kockerols, Pierre; Okkinga, Klaas [EC-JRC-Institute for Reference Materials and Measurements (IRMM), Retieseweg 111, B-2440 Geel (Belgium); Tagziria, Hamid [EC-JRC-Institute for the Protection and the Security of the Citizen (IPSC), Via E. Fermi 1, I-21020 Ispra (Vatican City State, Holy See,) (Italy); Vanhavere, Filip [SCK-CEN, Boeretang, 2400 Mol (Belgium); Wieslander, J.S. Elisabeth [EC-JRC-Institute for Reference Materials and Measurements (IRMM), Retieseweg 111, B-2440 Geel (Belgium); Department of Physics, P.O. Box 35 (YFL), FIN-40014, University of Jyvaeskylae (Finland)

    2009-01-15

    A simple and robust detector for spectrometry of environmental neutrons has been developed. The technique is based on neutron activation of a series of different metal disks followed by low-level gamma-ray spectrometry of the activated disks and subsequent neutron spectrum unfolding. The technique is similar to foil activation but here the applied neutron fluence rates are much lower than usually in the case of foil activation. The detector has been tested in quasi mono-energetic neutron fields with fluence rates in the order of 1000-10000 cm{sup -2} s{sup -1}, where the obtained spectra showed good agreement with spectra measured using a Bonner sphere spectrometer. The detector has also been tested using an AmBe source and at a neutron fluence rate of about 40 cm{sup -2} s{sup -1}, again, a good agreement with the assumed spectrum was achieved.

  7. Neutron activation analysis of automobile exhaust pollutants

    International Nuclear Information System (INIS)

    Oakes, T.W.; Furr, A.K.; Adair, D.J.; Parkinson, T.F.

    1977-01-01

    An approximation of the distribution of lead particulate from vehicular exhausts is given. Soil and grass (Poa trivialis) samples were collected at five-foot intervals from the roadside out to 300 feet, at ten-foot intervals from 300 to 350 feet, and at 25-foot intervals from 350 to 600 feet. All samples were irradiated twice: once for a brief period of from 10 to 120 seconds and later for periods of from 6 to 8 hours. The short irradiations were at a thermal neutron flux of 1.2x10 12 ncm -2 sec -1 (decay time=1 min, counting time=8 min). The long irradiations were at a thermal neutron flux of 1.3x10 12 ncm -2 sec -1 , and the samples counted twice at decay intervals of two days and twelve days. The counting intervals were one hour. The spectra were stored on magnetic tape for processing by an IBM 370/158 computer. This initial neutron-activation analysis study has shown that there is an extremely detailed pattern of the effluent from vehicular highway traffic which is strongly affected by micrometeorological conditions. In order to detect these patterns it is necessary to use a very compact sample grid with every possible precaution taken to ensure sample homogeneity and cleanliness. A possibility of elevated levels of pollution may exist at considerable distances from the highway, perhaps even greater than at the immediate roadside. (T.G.)

  8. Nitrogen determination in wheat by neutron activation analysis using fast neutron flux from a thermal nuclear reactor

    International Nuclear Information System (INIS)

    Ramirez G, T.

    1976-01-01

    This is a study of the technique for the determination of nitrogen and other elements in wheat flour through activation analysis with fast neutrons from a thermal nuclear reactor. The study begins with an introduction about the basis of the analytical methods, the equipment used in activation analysis and a brief description of the neutrons source. In the study are included the experiments carried out in order to determine the flux form in the site of irradiation, the N-13 half life and the interference due to the sample composition. (author)

  9. Data reduction for a high-throughput neutron activation analysis system

    International Nuclear Information System (INIS)

    Bowman, W.W.

    1979-01-01

    To analyze samples collected as part of a geochemical survey for the National Uranium Resource Evaluation program, Savannah River Laboratory has installed a high-throughput neutron activation analysis system. As part of that system, computer programs have been developed to reduce raw data to elemental concentrations in two steps. Program RAGS reduces gamma-ray spectra to lists of photopeak energies, peak areas, and statistical errors. Program RICHES determines the elemental concentrations from photopeak and delayed-neutron data, detector efficiencies, analysis parameters (neutron flux and activation, decay, and counting times), and spectrometric and cross-section data from libraries. Both programs have been streamlined for on-line operation with a minicomputer, each requiring approx. 64 kbytes of core. 3 tables

  10. Activation measurements for thermal neutrons. Part G. Natural 36Cl production in mineral samples

    International Nuclear Information System (INIS)

    Nolte, Eckehart; Huber, Thomas; Lazarev, Vitali; Ruehm, Werner; Kato, Kazuo; Schultz, Ludolf

    2005-01-01

    In the present paper, a method was developed to calculate the contribution of natural in situ production of 36 Cl in mineral samples to the 36 Cl signal induced by the neutrons from the Hiroshima bomb. Parameters used in the calculations include local erosion rates, lithospheric depth, and elemental composition for each investigated sample. It has been shown that the calculations agree within their uncertainties with 36 Cl values measured by means of accelerator mass spectrometry, in granite samples from quarries with known locations. Both calculations and measurements suggest typical 36 Cl/Cl ratios of about 10 -13 in mineral samples. (J.P.N.)

  11. Pulsed neutron generator for use with pulsed neutron activation techniques

    International Nuclear Information System (INIS)

    Rochau, G.E.

    1980-01-01

    A high-output, transportable, pulsed neutron generator has been developed by Sandia National Laboratories for use with Pulsed Neutron Activation (PNA) techniques. The PNA neutron generator generates > 10 10 14 MeV D-T neutrons in a 1.2 millisecond pulse. Each operation of the unit will produce a nominal total neutron output of 1.2 x 10 10 neutrons. The generator has been designed to be easily repaired and modified. The unit requires no additional equipment for operation or measurement of output

  12. Applied research and development of neutron activation analysis - The study on human health and environment by neutron activation analysis of biological samples

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Seung Yeon; Yoo, Jong Ik; Lee, Jae Kwang; Lee, Sung Jun; Lee, Sang Sun; Jeon, Ki Hong; Na, Kyung Won; Kang, Sang Hun [Yonsei University, Seoul (Korea)

    2000-04-01

    With the development of the precise quantitative analytical method for the analysis of trace elements in the various biological samples such as hair and food, evaluation in view of health and environment to the trace elements in various sources which can be introduced inside human body was done. The trace elemental distribution in Korean total diet and representative food stuff was identified first. With the project the elemental distributions in supplemental healthy food and Korean and Chinese origin oriental medicine were identified. The amount of trace elements ingested with the hair analysis of oriental medicine takers were also estimated. The amounts of trace elements inhaled with the analysis of foundry air, blood and hair of foundry workers were also estimated. The basic estimation method in view of health and environment with the neutron activation analysis of biological samples such as foods and hair was established with the result. Nationwide usage system of the NAA facility in Hanaro in many different and important areas of biological area can be initiated with the results. The output of the project can support public heath, environment, and medical research area. The results can be applied for the process of micronutrients enhanced health food production and for the health safety and health status enhancement with the additional necessary data expansion and the development of various evaluation technique. 19 refs., 7 figs., 23 tabs. (Author)

  13. Determination of iodine 129 in vegetables using neutron activation analysis

    International Nuclear Information System (INIS)

    Quintana, Eduardo E.; Thyssen, Sandra M.; Bruno, Hector A.

    1999-01-01

    The developed methodology allows the determination of iodine 129 in vegetables, using neutron activation analysis. The chemical treatment removes the interferences present in these matrixes, as well as the bromine 82 originated in the activation process. The experimental method for the determination of iodine 129 by neutron activation analysis involves five steps: 1- digestion by alkaline fusion; 2- pre-irradiation purification of iodine 129 by distillation followed by solvent extraction, and adsorption on activated charcoal by distillation; 3- neutron irradiation; 4- post-irradiation purification of iodine 130 by distillation followed by solvent extraction; 5- gamma spectrometry. A chemical recovery of 95 % is obtained in the distillations, measured using iodine 131 as tracer. The whole process recovery is within 70 % and 85 %. The detection limit is 2 mBq/kg of sample, but several factors affect this value, such as type of vegetable, natural iodine concentration, irradiation time and neutron flux. The methodology developed is applied at environmental surveillance with safeguards proposes, in the detection of undeclared reprocessing of irradiated fuel. (authors)

  14. Estimation of 129I by low energy spectrometry and neutron activation analysis

    International Nuclear Information System (INIS)

    Ravi, P.M.; Iyer, M.R.; Sahasrabudhe, S.G.; Somasundaram, S.; Subramanian, M.S.

    1986-01-01

    Methods have been developed for the estimation of 129 I by direct passive counting and by neutron activation analysis. The direct counting method using low energy photon spectrometry has been standardised for liquid samples. Interference from different induced radionuclides in the activation method was studied. Limits of detection of 129 I by direct counting method and neutron activation analysis work out to be 0.4 Bq and 1mBq respectively. (author). 6 refs

  15. Neutron activation analysis of atmospheric aerosol

    International Nuclear Information System (INIS)

    Obrusnik, I.

    1986-01-01

    Neutron activation analysis (NAA) is a modern analytical method well suited for the analysis of atmospheric aerosols. Particular steps of the NAA procedure and especially different types of aerosol sampling and sample preparation for analysis are discussed in detail. Several possible NAA techniques are described and the advantages of a purely instrumental technique with short and long irradiation are pointed out. Important performance characteristics of the NAA method such as precision, accuracy, sensitivity and detection limits are also discussed. Different applications of NAA in environmental studies are reviewed. (author)

  16. Analysis of human enamel and dentine by neutron activation analysis

    International Nuclear Information System (INIS)

    Soares, Marco A.B.

    2005-01-01

    Determination of trace elements in dental tissues has been of great interest to study the correlation between element composition and caries as well as food habits of individuals. In the present study dentine and enamel samples from healthy individuals were analysed by neutron activation analysis. The teeth were provided form dental clinics, and they were previously washed using purified water and acetone. Then they were dried at 40 deg C and ground in a agate mortar. The samples and element standards were irradiated with thermal neutrons at the IEA-R1 nuclear reactor. Long irradiations of 8 h under thermal neutron flux of 5x10 12 n cm -2 s -1 were used for Ca, Na, Sr and Zn determinations. In short irradiations of 15 s and under neutron flux of 10 12 n cm -2 s -1 the elements Mg, Mn, Na e Sr were determined. The induced gamma activities of the samples and standards were measured using a hyperpure Ge detector coupled to a gamma ray spectrometer. Elemental concentrations were calculated by comparative method. Results obtained showed that Ca, Mg and Na are present in both tissues at the level of percentages and the elements Mn, Sr and Zn at the μg g -1 levels. For quality control of the results the certified reference materials NIST 1400 Bone Ash and NIST 1486 Bone Meal were analysed. (author)

  17. Determination of phosphorus and calcium in biological samples by activation with 14 MeV neutrons; Determinacao de fosforo e calcio em amostras biologicas por ativacao com neutrons de 14 MeV

    Energy Technology Data Exchange (ETDEWEB)

    Berretta, Jose Roberto

    1995-07-01

    Analytical methods for phosphorus and calcium in biological samples by means of activation with 14 MeV neutrons, using the Van de Graaff accelerator from the Instituto de Pesquisas Energeticas e Nucleares, SP, Brazil are developed. For phosphorus analysis, powder samples were pressed into pellets, weighed and transferred to polyethylene plastic envelopes. The pellets with cadmium shielding were irradiated under a fast neutron flux for 5 to 10 minutes, and further counted in a HPGe detector for 5 minutes. Calcium analysis was performed by cyclic irradiation. Samples were irradiated for 10 minutes. After a decay time of 2 minutes, gamma counting was performed for 10 minutes. After a decay time of 2 minutes, a new irradiation ws made. The irradiation cycle was repeated 5 times and the counting spectrum obtained in each cycle was accumulated in the multi channel analyser. The variation of the neutron flux was followed by using a BF{sub 3} detector calibrated with and aluminium monitor. By means of the gamma spectrum and the neutron counting of the BF{sub 3} detector it was possible to estimate phosphorus and calcium concentrations in the sample analyzed. The methods were checked in the reference samples from the International Atomic Energy Agency and in commercial samples of powder milk, fertilizer and animal bone. Phosphorus contents in bone (A3/74) and milk (A-11) reference materials were (15.6 +- 1.8%) and (0.9 +- 0.1)%, respectively. These values are in good agreement to the certified values (15.5 +- 0.5)% and (0.910 +- 0.102)%, respectively. Calcium analysis carried out in bone (A3/74) presented a value of (31.8+-4.1)% and the certified value was of (31.3 +- 0.3)%. Detection limits for phosphorus and calcium were determined in different analyzed samples. The agreement of the results obtained with the certified values confirmed the suitability of the methods for phosphorus and calcium analysis. The methods are fast and laborious chemical procedures are not required

  18. Microscopic cross-section measurements by thermal neutron activation

    International Nuclear Information System (INIS)

    Avila L, J.

    1987-08-01

    Microscopic cross sections measured by thermal neutron activation using RP-0 reactor at the Peruvian Nuclear Energy Institute. The method consists in measuring microscopic cross section ratios through activated samples, requiring being corrected in thermal and epithermal energetic range by Westcott formalism. Furthermore, the comptage ratios measured for each photopeak to its decay fraction should be normalized from interrelation between both processes above, activation microscopic cross sections are obtained

  19. Neutron activation determination of iridium, gold, platinum, and silver in geologic samples

    International Nuclear Information System (INIS)

    Millard, H.T. Jr.

    1987-01-01

    In the procedure developed in this study, samples irradiated in the epithermal neutron facility of the U.S. Geological Survey TRIGA Reactor (Denver, Colorado) are treated with a mini-free assay technique. The iridium, gold, and silver are collected in a 1-gram metallic lead button. Primary contaminants at this stage are arsenic and antimony. These can be removed by heating the button with a mixture of sodium peroxide and sodium hydroxide. The resulting 0.2-gram lead bead is counted in a Compton suppression spectrometer. Carrier yields are determined by reirradiation of the lead beads. This procedure was applied to the U.S.G.S. Standard Rock PCC-1 and samples from K-T boundary sites in the Western Interior of North America. (author)

  20. Neutron activation analysis of sediment core samples of Lake Erhai in southern China and a Salt Lake in India

    International Nuclear Information System (INIS)

    Toyoda, Kazuhiro; Shinozuka, Yoshitsugu; Miura, Masahiro; Moriyasu, Yuki

    2005-01-01

    The purpose of this research is in the verification of the hypothesis that the long-lived nuclide ratio of Th/Sc in the deposit sample dug up in the lake with the hinterland of the granite quality is the index of a past change of precipitation and of the event such as earthquakes. As a preceding step the relation between an environmental change and a climate change was studied by the measuring result of the ratio of Th/Sc by the neutron activation analysis about the digging core sample of the Nepalese Katmandu basin (For the past 700,000 years) and the core sample (For 40,000 years and 8,000 years of the past) in Lake Biwa. (H. Katsuta)

  1. Texture investigation in aluminium and iron - silicon samples by neutron diffraction technique

    International Nuclear Information System (INIS)

    Pugliese, R.; Yamasaki, J.M.

    1988-09-01

    By means of the neutron diffraction technique the texture of 5% and 98% rolled-aluminium and of iron-silicon steel used in the core of electric transformers, have been determined. The measurements were performed by using a neutron diffractometer installed at the IEA-R1 Nuclear Research Reactor, in the Beam-Hole n 0 . 6. To avoid corrections such as neutron absorption and sample luminosity the geometric form of the samples were approximated to spheric or octagonal prism, and its dimensions do not exceed that of the neutron beam. The texture of the samples were analysed with the help of a computer programme that analyses the intensity of the diffracted neutron beam and plot the pole figures. (author) [pt

  2. Neutron activation analysis of artefacts

    International Nuclear Information System (INIS)

    Mohd Suhaimi Hamzah; Shamsiah Abd Rahman

    2004-01-01

    The paper discussed the utilization of neutron activation analysis in this field. NAA, an analytical technique which analyzing the elements in the sample without any chemical treatment. It is sensitive and accurate. Archaeological objects i.e. ceramics, historical building materials, metals, etc can be analyze with this technique. The analysis results were presented in form of characterization of the artefacts in chemical profiles, which can present the information of the origin of the artefacts as well as it originality. (Author)

  3. Partial neutron capture cross sections of actinides using cold neutron prompt gamma activation analysis

    International Nuclear Information System (INIS)

    Genreith, Christoph

    2015-01-01

    Nuclear waste needs to be characterized for its safe handling and storage. In particular long-lived actinides render the waste characterization challenging. The results described in this thesis demonstrate that Prompt Gamma Neutron Activation Analysis (PGAA) with cold neutrons is a reliable tool for the non-destructive analysis of actinides. Nuclear data required for an accurate identification and quantification of actinides was acquired. Therefore, a sample design suitable for accurate and precise measurements of prompt γ-ray energies and partial cross sections of long-lived actinides at existing PGAA facilities was presented. Using the developed sample design the fundamental prompt γ-ray data on 237 Np, 241 Am and 242 Pu were measured. The data were validated by repetitive analysis of different samples at two individual irradiation and counting facilities - the BRR in Budapest and the FRM II in Garching near Munich. Employing cold neutrons, resonance neutron capture by low energetic resonances was avoided during the experiments. This is an improvement over older neutron activation based works at thermal reactor neutron energies. 152 prompt γ-rays of 237 Np were identified, as well as 19 of 241 Am, and 127 prompt γ-rays of 242 Pu. In all cases, both high and lower energetic prompt γ-rays were identified. The most intense line of 237 Np was observed at an energy of E γ =182.82(10) keV associated with a partial capture cross section of σ γ =22.06(39) b. The most intense prompt γ-ray lines of 241 Am and of 242 Pu were observed at E γ =154.72(7) keV with σ γ =72.80(252) b and E γ =287.69(8) keV with σ γ =7.07(12) b, respectively. The measurements described in this thesis provide the first reported quantifications on partial radiative capture cross sections for 237 Np, 241 Am and 242 Pu measured simultaneously over the large energy range from 45 keV to 12 MeV. Detailed uncertainty assessments were performed and the validity of the given uncertainties was

  4. 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)

  5. Effect of sample moisture and bulk density on performance of the 241Am-Be source based prompt gamma rays neutron activation analysis setup. A Monte Carlo study

    International Nuclear Information System (INIS)

    Almisned, Ghada

    2010-01-01

    Monte Carlo simulations were carried out using the dependence of gamma ray yield on the bulk density and moisture content for five different lengths of Portland cement samples in a thermal neutron capture based Prompt Gamma ray Neutron Activation Analysis (PGNAA) setup for source inside moderator geometry using an 241 Am-Be neutron source. In this study, yields of 1.94 and 6.42 MeV prompt gamma rays from calcium in the five Portland cement samples were calculated as a function of sample bulk density and moisture content. The study showed a strong dependence of the 1.94 and 6.42 MeV gamma ray yield upon the sample bulk density but a weaker dependence upon sample moisture content. For an order of magnitude increase in the sample bulk density, an order of magnitude increase in the gamma rays yield was observed, i.e., a one-to-one correspondence. In case of gamma ray yield dependence upon sample moisture content, an order of magnitude increase in the moisture content of the sample resulted in about 16-17% increase in the yield of 1.94 and 6.42 MeV gamma rays from calcium. (author)

  6. A PC-program for the calculation of neutron flux and element contents using the ki-method of neutron activation analysis

    International Nuclear Information System (INIS)

    Boulyga, E.G.; Boulyga, S.F.

    2000-01-01

    A computer program is described, which calculates the induced activities of isotopes after irradiation in a known neutron field, thermal and epithermal neutron fluxes from the measured induced activities and from nuclear data of 2-4 monitor nuclides as well as the element concentrations in samples irradiated together with the monitors. The program was developed for operation in Windows 3.1 (or higher). The application of the program for neutron activation analysis allows to simplify the experimental procedure and to reduce the time. The program was tested by measuring different types of standard reference materials at the FRJ-2 (Research Centre, Juelich, Germany) and Triga (University Mainz, Germany) reactors. Comparison of neutron flux parameters calculated by this program with those calculated by a VAX program developed at the Research Centre, Juelich was done. The results of testing seem to be satisfactory. (author)

  7. Neutron-Irradiated Samples as Test Materials for MPEX

    International Nuclear Information System (INIS)

    Ellis, Ronald James; Rapp, Juergen

    2015-01-01

    Plasma Material Interaction (PMI) is a major concern in fusion reactor design and analysis. The Material-Plasma Exposure eXperiment (MPEX) will explore PMI under fusion reactor plasma conditions. Samples with accumulated displacements per atom (DPA) damage produced by fast neutron irradiations in the High Flux Isotope Reactor (HFIR) at Oak Ridge National Laboratory (ORNL) will be studied in the MPEX facility. This paper presents assessments of the calculated induced radioactivity and resulting radiation dose rates of a variety of potential fusion reactor plasma-facing materials (such as tungsten). The scientific code packages MCNP and SCALE were used to simulate irradiation of the samples in HFIR including the generation and depletion of nuclides in the material and the subsequent composition, activity levels, gamma radiation fields, and resultant dose rates as a function of cooling time. A challenge of the MPEX project is to minimize the radioactive inventory in the preparation of the samples and the sample dose rates for inclusion in the MPEX facility

  8. Neutron activation analysis of high purity tellurium

    International Nuclear Information System (INIS)

    Gil'bert, Eh.N.; Verevkin, G.V.; Obrazovskij, E.G.; Shatskaya, S.S.

    1980-01-01

    A scheme of neutron activation analysis of high purity tellurium is developed. Weighed amount of Te (0.5 g) is irradiated for 20-40 hr in the flux of 2x10 13 neutron/(cm 2 xs). After decomposition of the sample impurities of gold and palladium are determined by the extraction with organic sulphides. Tellurium separation from the remaining impurities is carried out by the extraction with monothiobenzoic acid from weakly acidic HCl solutions in the presence of iodide-ions, suppressing silver extraction. Remaining impurity elements in the refined product are determined γ-spectrometrically. The method allows to determine 34 impurities with determination limits 10 -6 -10 -11 g

  9. Utilization and facility of neutron activation analysis in HANARO research reactor

    International Nuclear Information System (INIS)

    Chung, Y.S.; Chung, Y.J.; Moon, J.H.

    1998-01-01

    The facilities of neutron activation analysis within a multi-purpose research reactor (HANARO) are described and the main applications of Neutron activation analysis (NAA) in Korea are reviewed. The sample irradiation tube, automatic and manual pneumatic transfer system, are installed at three irradiation holes. One irradiation hole is lined with a cadmium tube for epithermal-nal NAA. The performance of the NAA facility was examined to identify the characteristics of tube transfer system, irradiation sites and polyethylene irradiation capsule. The available thermal neutron flux with each irradiation site are in the range of 3.9x10 13 -1.6x10 14 n/cm 2 ·s and cadmium ratios are 15-250. Neutron activation analysis has been applied in the trace component analysis of nuclear, geological, biological, environmental and high purity materials and various polymers for research and development. Analytical services and the latest analytical results are summarized. (author)

  10. Certification of standard reference materials employing neutron activation analysis

    International Nuclear Information System (INIS)

    Capote Rodriguez, G.; Hernandez Rivero, A.; Molina Insfran, J.; Ribeiro Guevara, S.; Santana Encinosa, C.; Perez Zayas, G.

    1997-01-01

    Neutron activation analysis (Naa) is used extensively as one of the analytical techniques in the certification of standard reference materials (Srm). Characteristics of Naa which make it valuable in this role are: accuracy; multielemental capability; ability to assess homogeneity; high sensitivity for many elements, and essentially non-destructive method. This paper reports the concentrations of thirty elements (major, minor and trace elements) in four Cuban Srm's. The samples were irradiated in a thermal neutron flux of 10 12 -10 13 neutrons.cm -2 .s -1 . The gamma-ray spectra were measured by HPGe detectors and were analysed using ACTAN program, developed in CEADEN. (author) [es

  11. Radioactive waste characterisation by neutron activation

    International Nuclear Information System (INIS)

    Nicol, Tangi

    2016-01-01

    Nuclear activities produce radioactive wastes classified following their radioactive level and decay time. an accurate characterization is necessary for efficient classification and management. Medium and high level wastes containing long lived radioactive isotopes will be stored in deep geological storage for hundreds of thousands years. at the end of this period, it is essential to ensure that the wastes do not represent any risk for humans and environment, not only from radioactive point of view, but also from stable toxic chemicals. This PhD thesis concerns the characterization of toxic chemicals and nuclear material in radioactive waste, by using neutron activation analysis, in the frame of collaboration between the Nuclear Measurement Laboratory of CEA Cadarache, France, and the Institute of Nuclear Waste Management and Reactor Safety of the research center, FZJ (Forschungszentrum Juelich GmbH), Germany. The first study is about the validation of the numerical model of the neutron activation cell MEDINA (FZJ), using MCNP Monte Carlo transport code. Simulations and measurements of prompt capture gamma rays from small samples measured in MEDINA have been compared for a number of elements of interest (beryllium, aluminum, chlorine, copper, selenium, strontium, and tantalum). The comparison was performed using different nuclear databases, resulting in satisfactory agreement and validating simulation in view of following studies. Then, the feasibility of fission delayed gamma-ray measurements of "2"3"9Pu and "2"3"5U in 225 L waste drums has been studied, considering bituminized or concrete matrixes representative of wastes produced in France and Germany. The delayed gamma emission yields were first determined from uranium and plutonium metallic samples measurements in REGAIN, the neutron activation cell of LMN, showing satisfactory consistency with published data. The useful delayed gamma signals of "2"3"9Pu and "2"3"5U, homogeneously distributed in the 225 L

  12. Determination of sodium in pharmaceuticals by neutron activation analysis

    International Nuclear Information System (INIS)

    Kanias, G.D.

    1985-01-01

    A simple, fast and accurate neutron activation analysis method for determination of Na in drugs concerning either active compound or total content was developed. The examined dosage forms consisted of 10 injectable ampoules and 10 bottles of oral solutions. The irradiation of samples and standards was carried out in the rotation system of the Reactor of Nuclear Research Center Democritos with maximal neutron flux of 2,9.10 13 n.cm -2 .sec -1 . Gamma-ray spectrometry of the irradiated samples and standards was accomplished with a coaxial Ge(Li) detector series Win 15 with an efficiency of 15% connected to an Ino-Tech 1024 channel analyser (Model IT 5200). The accuracy and precision of the method are found to be very high and therefore it could be established as an official one for the determination of sodium in parmaceuticals

  13. Effects of (α,n) contaminants and sample multiplication on statistical neutron correlation measurements

    International Nuclear Information System (INIS)

    Dowdy, E.J.; Hansen, G.E.; Robba, A.A.; Pratt, J.C.

    1980-01-01

    The complete formalism for the use of statistical neutron fluctuation measurements for the nondestructive assay of fissionable materials has been developed. This formalism includes the effect of detector deadtime, neutron multiplicity, random neutron pulse contributions from (α,n) contaminants in the sample, and the sample multiplication of both fission-related and background neutrons

  14. Neutronics activities for next generation devices

    International Nuclear Information System (INIS)

    Gohar, Y.

    1985-01-01

    Neutronic activities for the next generation devices are the subject of this paper. The main activities include TFCX and FPD blanket/shield studies, neutronic aspects of ETR/INTOR critical issues, and neutronics computational modules for the tokamak system code and tandem mirror reactor system code. Trade-off analyses, optimization studies, design problem investigations and computational models development for reactor parametric studies carried out for these activities are summarized

  15. A novel method for active fissile mass estimation with a pulsed neutron source

    International Nuclear Information System (INIS)

    Dubi, C.; Ridnik, T.; Israelashvili, I.; Pedersen, B.

    2013-01-01

    Neutron interrogation facilities for mass evaluation of Special Nuclear Materials (SNM) samples are divided into two main categories: passive interrogation, where all neutron detections are due to spontaneous events, and active interrogation, where fissions are induced on the tested material by an external neutron source. While active methods are, in general, faster and more effective, their analysis is much harder to carry out. In the paper, we will introduce a new formalism for analyzing the detection signal generated by a pulsed source active interrogation facility. The analysis is aimed to distinct between fission neutrons from the main neutron source in the system, and the surrounding “neutron noise”. In particular, we derive analytic expressions for the first three central moments of the number of detections in a given time interval, in terms of the different neutron sources. While the method depends on exactly the same physical assumptions as known models, the simplicity of the suggested formalism allows us to take into account the variance of the external neutron source—an effect that was so far neglected

  16. A novel method for active fissile mass estimation with a pulsed neutron source

    Energy Technology Data Exchange (ETDEWEB)

    Dubi, C., E-mail: chendb331@gmail.com [Physics Department, Nuclear Research Center of the Negev, POB 9001, Beer Sheva (Israel); Ridnik, T.; Israelashvili, I. [Physics Department, Nuclear Research Center of the Negev, POB 9001, Beer Sheva (Israel); Pedersen, B. [Nuclear Security Unit, Institute for Transuranium Elements, Via E. Fermi, 2749 JRC, Ispra (Italy)

    2013-07-01

    Neutron interrogation facilities for mass evaluation of Special Nuclear Materials (SNM) samples are divided into two main categories: passive interrogation, where all neutron detections are due to spontaneous events, and active interrogation, where fissions are induced on the tested material by an external neutron source. While active methods are, in general, faster and more effective, their analysis is much harder to carry out. In the paper, we will introduce a new formalism for analyzing the detection signal generated by a pulsed source active interrogation facility. The analysis is aimed to distinct between fission neutrons from the main neutron source in the system, and the surrounding “neutron noise”. In particular, we derive analytic expressions for the first three central moments of the number of detections in a given time interval, in terms of the different neutron sources. While the method depends on exactly the same physical assumptions as known models, the simplicity of the suggested formalism allows us to take into account the variance of the external neutron source—an effect that was so far neglected.

  17. Activation Inventories after Exposure to DD/DT Neutrons in Safety Analysis of Nuclear Fusion Installations.

    Science.gov (United States)

    Stankunas, Gediminas; Cufar, Aljaz; Tidikas, Andrius; Batistoni, Paola

    2017-11-23

    Irradiations with 14 MeV fusion neutrons are planned at Joint European Torus (JET) in DT operations with the objective to validate the calculation of the activation of structural materials in functional materials expected in ITER and fusion plants. This study describes the activation and dose rate calculations performed for materials irradiated throughout the DT plasma operation during which the samples of real fusion materials are exposed to 14 MeV neutrons inside the JET vacuum vessel. Preparatory activities are in progress during the current DD operations with dosimetry foils to measure the local neutron fluence and spectrum at the sample irradiation position. The materials included those used in the manufacturing of the main in-vessel components, such as ITER-grade W, Be, CuCrZr, 316 L(N) and the functional materials used in diagnostics and heating systems. The neutron-induced activities and dose rates at shutdown were calculated by the FISPACT code, using the neutron fluxes and spectra that were provided by the preceding MCNP neutron transport calculations. © The Author 2017. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  18. Semiautomatic exchanger of samples for carry out neutron activation analysis; Intercambiador semiautomatico de muestras para realizar analisis por activacion neutronica

    Energy Technology Data Exchange (ETDEWEB)

    Aguilar H, F.; Quintana C, G. [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico); Torres R, C. E.; Mejia J, J. O., E-mail: fortunato.aguilar@inin.gob.mx [Instituto Tecnologico de Toluca, Av. Tecnologico s/n, Ex-Rancho La Virgen, Metepec, Estado de Mexico (Mexico)

    2015-09-15

    In this paper the design methodology and implementation of a semiautomatic exchanger of samples for the Analysis Laboratory by Neutron Activation of the Reactor department is presented. Taking into account the antecedents, the necessities of improvement are described, as well as the equipment that previously contained the Laboratory. The project of the semiautomatic exchanger of samples was developed at Instituto Nacional de Investigaciones Nucleares, with its own technology to increase independence from commercial equipment. Each element of the semiautomatic exchanger of samples is described both in the design phase as construction. The achieved results are positive and encouraging for the fulfillment of the proposed objective that is to increase the capacity of the Laboratory. (Author)

  19. Effect of granulation of geological samples in neutron transport measurements

    International Nuclear Information System (INIS)

    Woznicka, Urszula; Drozdowicz, Krzysztof; Gabanska, Barbara; Krynicka, Ewa; Igielski, Andrzej

    2001-01-01

    The thermal neutron absorption cross section is one of the parameters describing the transport of thermal neutrons in a medium. Theoretical descriptions and experiments which determine the absorption cross section have a wide literature for homogeneous media. The situation comes true e.g. for fluids or amorphous solids. There are many other media which should be treated as heterogeneous. Among others - geological materials. The material heterogeneity for the thermal neutron transport in a considered volume is understood here as an existence of many small regions which differ significantly in their macroscopic neutron diffusion parameters (defined by the absorption and transport cross sections). The final difference, which influences the neutron transport, comes from a combination of the absolute differences between the parameters and of sizes of regions (related to the neutron mean free paths). A rock can be naturally heterogeneous in the above meaning. Besides, it can happen that a preparation of the rock sample for a neutron measurement can increase its natural heterogeneity. (For example, when the rock material is crushed and the measured sample consists of the obtained grains). The question is which granulation is allowed to treat the sample material as still homogeneous, and from which size of the rock grains we have to consider a two-component medium. It has been experimentally proved that the effective absorption of thermal neutrons in a heterogeneous two-component material can significantly differ from the absorption in a homogeneous one which consists of the same elements. The final effect is dependent on a few factors: the macroscopic absorption cross sections of the components, their total mass contributions, and the size of the grains. The ratio of the effective absorption cross section of the heterogeneous material to the cross section of the equivalent homogeneous, is a measure of the heterogeneity effect on the thermal neutron absorption

  20. Validation and uncertainty estimation of fast neutron activation analysis method for Cu, Fe, Al, Si elements in sediment samples

    International Nuclear Information System (INIS)

    Sunardi; Samin Prihatin

    2010-01-01

    Validation and uncertainty estimation of Fast Neutron Activation Analysis (FNAA) method for Cu, Fe, Al, Si elements in sediment samples has been conduced. The aim of the research is to confirm whether FNAA method is still matches to ISO/lEC 17025-2005 standard. The research covered the verification, performance, validation of FNM and uncertainty estimation. Standard of SRM 8704 and sediments were weighted for certain weight and irradiated with 14 MeV fast neutron and then counted using gamma spectrometry. The result of validation method for Cu, Fe, Al, Si element showed that the accuracy were in the range of 95.89-98.68 %, while the precision were in the range 1.13-2.29 %. The result of uncertainty estimation for Cu, Fe, Al, and Si were 2.67, 1.46, 1.71 and 1.20 % respectively. From this data, it can be concluded that the FNM method is still reliable and valid for element contents analysis in samples, because the accuracy is up to 95 % and the precision is under 5 %, while the uncertainty are relatively small and suitable for the range 95 % level of confidence where the uncertainty maximum is 5 %. (author)

  1. Provenance study of ancient Chinese Yaozhou porcelain by neutron activation analysis

    International Nuclear Information System (INIS)

    Li, R.W.; Zhao, W.J.; Li, G.X.; Xie, J.Z.; Guo, M.; Gao, Z.Y.; Feng, S.L.; Fan, D.Y.; Zhang, Y.; Cai, Z.F.; Zhuo, Z.X.

    2004-01-01

    The glaze samples of ancient Chinese Yaozhou porcelain were analyzed by neutron activation analysis (NAA). The contents of 29 elements for each sample were measured. the scattergram of the coloring elements shows some informations of soueces of raw materials. (authors)

  2. On neutron activation analysis with γγ coincidence spectrometry

    International Nuclear Information System (INIS)

    Zeisler, Rolf; Danyal Turkoglu; Ibere Souza Ribeiro Junior; Shetty, M.G.

    2017-01-01

    A new γγ coincidence system has been set up at NIST. It is operated with a digital data finder supported by new software developed at NIST. The system is used to explore possible enhancements in instrumental neutron activation analysis (INAA) and study applicability to neutron capture prompt gamma activation analysis (PGAA). The performance of the system is tested with certified reference materials for efficiency calibration and quantitative performance. Comparisons of INAA results based on conventional gamma-ray spectrometry data with INAA results based on coincidence data obtained from the same samples show improvements in the counting uncertainties and demonstrates the quantitative accuracy of the new system. (author)

  3. Uses of instrumental neutron activation analysis (INAA) for lichen as bio indicators of environmental contamination

    International Nuclear Information System (INIS)

    Arribere, M.; Guevara, S.R.; Calvelo, S.

    1994-01-01

    Three species of epiphytic lichens were sampled at NW Patagonia, Argentina, from urban and peripherical forest area environments Sixty lichen samples were analysed individually by Instrumental Neutron Activation Analysis (INAA). The elements present in the samples were determined by parametric methods at the Neutron Activation Laboratory at Centro Atomico Bariloche, Argentina. All concentration values were normalized to Al concentration. The average normalized concentrations for each element, discriminated by species and environment, are presented in this work. (author). 11 refs, 6 tabs

  4. Neutron activation analysis of Permian-Triassic boundary layer samples at the Selong Site in China

    International Nuclear Information System (INIS)

    Miyamoto, Y.; Sakamoto, K.; Mingqing, W.

    1997-01-01

    Thirty samples from a limestone stratum across the Permian-Triassic (P-Tr) boundary layer in China were analyzed for 30 elements by instrumental neutron activation analysis, wavelength dispersive X-ray fluorescence and ICP-MS, and also for mineral compositions with a powder X-ray diffractometer. The depth profile was found to indicate a sudden change of elemental and mineral compositions across the P-Tr boundary. Also the profile showed several peaks in elemental concentrations in the lower Permian layered samples as well as in the overlying Triassic strata, which are associated with the change of mineral compositions. Elemental profiles were found to be classified into 4 groups and to give some insights in the geochemical records. Ir is far less abundant (0.1 ppt) compared with that of the K-T boundaries (10 ppb), and the Ir/Co ratio is outside the K-T and Cl chondrite trends. This change of elementary profile is suggestive of the internal causes rather than the external ones such as an asteroid impact for the mass extinction at the P-Tr boundary. (author)

  5. Elemental analysis of soil and plant samples at El-Manzala lake neutron activation analysis technique. Vol. 4

    Energy Technology Data Exchange (ETDEWEB)

    Eissa, E A; Rofail, N B; Hassan, A M [Reactor and Neutron Physics Department, Nuclear Research Center, Atomic Energy Authority, Cairo (Egypt); Abd El-Haleem, A S [Radiactive Environment Pollution Department, Hot Laboratories Center, Nuclear Research Center, Atomic Energy Authority, Cairo (Egypt); El-Abbady, W H [Phsics Department, Faculty of Science , Al-Azhar University, (Egypt)

    1996-03-01

    Soil and plant samples were collected from from two locations, Bahr El-Baker, and Bahr kados at the manzala lake, where, where high pollution is expected. The samples were especially treated and prepared for investigation by thermal neutron activation analysis (NAA). The irradiation facilities of the first egyptian research reactor (ET-R R-1), and the hyper pure germanium (HPGe) detection system were used for analysis. Among the 34 identified Fe, Co, As, Cd, Te, La, Sm, Rb, Hg, Th, and U are of a special significance because of the their toxic deleterious impact on living organisms. This work is part of a research project concerning pollution studies on the river Nile and some lakes of egypt. The data obtained in the present work stands as a reference basic record for any future follow up of contamination level. 1 tab.

  6. Simultaneous multi-element determination in different seed samples of Dodonaea viscosa hopseed using instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    El-Sweify, Fatma H.; El-Amir, Mahmoud A.; Mostafa, Mohamed; Ramadan, Hala E.; Rashad, Ghada M.

    2016-01-01

    Instrumental neutron activation analysis technique (INAA) was applied for nondestructive multi-element analysis of seed samples of the plant Dodonaea viscosa hopseed. This plant is distributed all over Egypt, because of its suitable properties. The samples were collected from some bushes grown at different sites in some governorates, in July of each year during the period from 2004 to 2011. The determined elements are: Co, Cs, Eu, Fe, Hg, Ni, Rb, Sc, Se, Sr and Zn, under the chosen irradiation and cooling times. The content of some elements has been compared with data obtained from previous work on analysis of various kinds of seeds. The influence of some parameters on the determined elemental content is discussed. Standard reference materials IAEA-155 and IAEA-V-10 were used to assure quality control, accuracy and precision of the technique.

  7. Elemental analysis of soil and plant samples at El-Manzala lake neutron activation analysis technique. Vol. 4

    International Nuclear Information System (INIS)

    Eissa, E.A.; Rofail, N.B.; Hassan, A.M.; Abd El-Haleem, A.S.; El-Abbady, W.H.

    1996-01-01

    Soil and plant samples were collected from from two locations, Bahr El-Baker, and Bahr kados at the manzala lake, where, where high pollution is expected. The samples were especially treated and prepared for investigation by thermal neutron activation analysis (NAA). The irradiation facilities of the first egyptian research reactor (ET-R R-1), and the hyper pure germanium (HPGe) detection system were used for analysis. Among the 34 identified Fe, Co, As, Cd, Te, La, Sm, Rb, Hg, Th, and U are of a special significance because of the their toxic deleterious impact on living organisms. This work is part of a research project concerning pollution studies on the river Nile and some lakes of egypt. The data obtained in the present work stands as a reference basic record for any future follow up of contamination level. 1 tab

  8. Simultaneous multi-element determination in different seed samples of Dodonaea viscosa hopseed using instrumental neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    El-Sweify, Fatma H.; El-Amir, Mahmoud A.; Mostafa, Mohamed; Ramadan, Hala E.; Rashad, Ghada M. [Atomic Energy Authority, Cairo (Egypt). Hot Lab. Center

    2016-07-01

    Instrumental neutron activation analysis technique (INAA) was applied for nondestructive multi-element analysis of seed samples of the plant Dodonaea viscosa hopseed. This plant is distributed all over Egypt, because of its suitable properties. The samples were collected from some bushes grown at different sites in some governorates, in July of each year during the period from 2004 to 2011. The determined elements are: Co, Cs, Eu, Fe, Hg, Ni, Rb, Sc, Se, Sr and Zn, under the chosen irradiation and cooling times. The content of some elements has been compared with data obtained from previous work on analysis of various kinds of seeds. The influence of some parameters on the determined elemental content is discussed. Standard reference materials IAEA-155 and IAEA-V-10 were used to assure quality control, accuracy and precision of the technique.

  9. Measurements of fusion neutron yields by neutron activation technique: Uncertainty due to the uncertainty on activation cross-sections

    Energy Technology Data Exchange (ETDEWEB)

    Stankunas, Gediminas, E-mail: gediminas.stankunas@lei.lt [Lithuanian Energy Institute, Laboratory of Nuclear Installation Safety, Breslaujos str. 3, LT-44403 Kaunas (Lithuania); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Batistoni, Paola [ENEA, Via E. Fermi, 45, 00044 Frascati, Rome (Italy); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom); Sjöstrand, Henrik; Conroy, Sean [Department of Physics and Astronomy, Uppsala University, PO Box 516, SE-75120 Uppsala (Sweden); EUROfusion Consortium, JET, Culham Science Centre, Abingdon OX14 3DB (United Kingdom)

    2015-07-11

    The neutron activation technique is routinely used in fusion experiments to measure the neutron yields. This paper investigates the uncertainty on these measurements as due to the uncertainties on dosimetry and activation reactions. For this purpose, activation cross-sections were taken from the International Reactor Dosimetry and Fusion File (IRDFF-v1.05) in 640 groups ENDF-6 format for several reactions of interest for both 2.5 and 14 MeV neutrons. Activation coefficients (reaction rates) have been calculated using the neutron flux spectra at JET vacuum vessel, both for DD and DT plasmas, calculated by MCNP in the required 640-energy group format. The related uncertainties for the JET neutron spectra are evaluated as well using the covariance data available in the library. These uncertainties are in general small, but not negligible when high accuracy is required in the determination of the fusion neutron yields.

  10. Design and building of a homemade sample changer for automation of the irradiation in neutron activation analysis technique

    International Nuclear Information System (INIS)

    Gago, Javier; Hernandez, Yuri; Baltuano, Oscar; Bedregal, Patricia; Lopez, Yon; Urquizo, Rafael

    2014-01-01

    Because the RP-10 research reactor operates during weekends, it was necessary to design and build a sample changer for irradiation as part of the automation process of neutron activation analysis technique. The device is formed by an aluminum turntable disk which can accommodate 19 polyethylene capsules, containing samples to be sent using the pneumatic transfer system from the laboratory to the irradiation position. The system is operate by a control switchboard to send and return capsules in a variable preset time and by two different ways, allowing the determination of short, medium and long lived radionuclides. Also another mechanism is designed called 'exchange valve' for changing travel paths (pipelines) allowing the irradiated samples to be stored for a longer time in the reactor hall. The system design has allowed complete automation of this technique, enabling the irradiation of samples without the presence of an analyst. The design, construction and operation of the device is described and presented in this article. (authors).

  11. Neutron activation analysis of neonate and maternal hair sampled in areas with different levels of pollution

    International Nuclear Information System (INIS)

    Obrusnik, I.; Skrivanek, O.; Umlaufova, M.; Hovorka, V.

    1985-01-01

    Instrumental neutron activation analysis was performed on human head hair of newborns and mothers sampled in two areas with different levels of environmental exposure. The group of neonates from the exposed area (polluted by thermal power plants burning brown coal and by chemical industry) exhibited higher levels of several trace elements in hair, e.g. Se, Zn, Hg and Sb in comparison with the control group. Moreover, the mean concentrations of Se, Hg, Zn and Br in neonate hair were found to be higher than in mothers' hair. Although the study revealed statistically significant differences in the composition of neonate hair samples in areas with different levels of environmental exposure, the differences are relatively small. Only a thorough long-term study both with environmental and medical observations can prove a direct connection of the elevated levels of some trace elements in neonate hair with the higher incidence of mental diseaes of children living in the exposed area. (author)

  12. Neutron activation analysis of archaeological artifacts using the conventional relative method: a realistic approach for analysis of large samples

    International Nuclear Information System (INIS)

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

    2012-01-01

    A new approach for analysis of entire potsherds of archaeological interest by INAA, using the conventional relative method, is described. The analytical method proposed involves, primarily, the preparation of replicates of the original archaeological pottery, with well known chemical composition (standard), destined to be irradiated simultaneously, in a well thermalized external neutron beam of the RP-10 reactor, with the original object (sample). The basic advantage of this proposal is to avoid the need of performing complicated effect corrections when dealing with large samples, due to neutron self shielding, neutron self-thermalization and gamma ray attenuation. In addition, and in contrast with the other methods, the main advantages are the possibility of evaluating the uncertainty of the results and, fundamentally, validating the overall methodology. (author)

  13. Possibilities of using neutron activation analysis to discovery antimony aureoles at near-surface deposits

    International Nuclear Information System (INIS)

    Voin, M.I.; Kuligin, V.M.; Rakovskij, Eh.E.

    1978-01-01

    Described is the technique for determining antimony in rock and ore samples by instrumental neutron activation method with the sensitivity of 0.5 g/t from the 0.3-0.5 g weighed amount. Antimony was determined using the photopeak of antimony-124 isotope with the energy of 1692 keV. For analysis, 0.1 g samples were packed in aluminium foil and irradiated for 22 hours by reactor neutron fluence of 1.2x10 13 neutron/cm 2 xs. After cooling for 7 days induced activity of samples was measured using multichannel analizer with semiconductor detector with sensitive zone volume of 40 cm 3 . Real sensitivity while determining antimony was 1g/t, mean square error in the content range of 1-10 g/t is 14%

  14. Krypton and xenon in Apollo 14 samples - Fission and neutron capture effects in gas-rich samples

    Science.gov (United States)

    Drozd, R.; Hohenberg, C.; Morgan, C.

    1975-01-01

    Gas-rich Apollo 14 breccias and trench soil are examined for fission xenon from the decay of the extinct isotopes Pu-244 and I-129, and some samples have been found to have an excess fission component which apparently was incorporated after decay elsewhere and was not produced by in situ decay. Two samples have excess Xe-129 resulting from the decay of I-129. The excess is correlated at low temperatures with excess Xe-128 resulting from neutron capture on I-127. This neutron capture effect is accompanied by related low-temperature excesses of Kr-80 and Kr-82 from neutron capture on the bromine isotopes. Surface correlated concentrations of iodine and bromine are calculated from the neutron capture excesses.

  15. Utilization and facility of neutron activation analysis in HANARO research reactor

    Energy Technology Data Exchange (ETDEWEB)

    Chung, Y S; Chung, Y J; Moon, J H [Korea Atomic Energy Research Institute, P.O.Box 105 Yusong, 305-600, Taejon (Korea, Republic of)

    1998-07-01

    The facilities of neutron activation analysis within a multi-purpose research reactor (HANARO) are described and the main applications of Neutron activation analysis (NAA) in Korea are reviewed. The sample irradiation tube, automatic and manual pneumatic transfer system, are installed at three irradiation holes. One irradiation hole is lined with a cadmium tube for epithermal-nal NAA. The performance of the NAA facility was examined to identify the characteristics of tube transfer system, irradiation sites and polyethylene irradiation capsule. The available thermal neutron flux with each irradiation site are in the range of 3.9x10{sup 13}-1.6x10{sup 14} n/cm{sup 2}{center_dot}s and cadmium ratios are 15-250. Neutron activation analysis has been applied in the trace component analysis of nuclear, geological, biological, environmental and high purity materials and various polymers for research and development. Analytical services and the latest analytical results are summarized. (author)

  16. Automation of registration of sample weights for high-volume neutron activation analysis at the IBR-2 reactor of FLNP, JINR

    International Nuclear Information System (INIS)

    Dmitriev, A.Yu.; Dmitriev, F.A.

    2015-01-01

    The 'Weight' software tool was created at FLNP JINR to automate the reading of analytical balance readouts and saving these values in the NAA database. The analytical balance connected to the personal computer is used to measure weight values. The 'Weight' software tool controls the reading of weight values and the exchange of information with the NAA database. The weighing process of a large amount of samples is reliably provided during high-volume neutron activation analysis. [ru

  17. Neutron activation analysis at the 'Instituto de Pesquisas Energeticas e Nucleares' (SP, Brazil)

    International Nuclear Information System (INIS)

    Vasconcellos, M.B.A.

    1984-01-01

    A review of the work carried out at IPEN using neutron activation analysis is made. The main characteristics of the technique and general experimental procedures applied for different samples and elements are reported. Geological samples were analysed by using activation with thermal, epithermal and delayed neutrons (for U and Th, specifically). Metallic samples were analysed for several elements in trace amounts (Ta in Nb, Hg in steel, Sn, Sb, As, Cu, Cr and Ag in a tin-lead alloy). Biological materials, such as tomatoes, animal and human viscera, food, hair, nails were also analysed for several components (Hg, Na, K, As, Au and others). (Author) [pt

  18. Imaging of heterogeneous materials by prompt gamma-ray neutron activation analysis

    International Nuclear Information System (INIS)

    Staples, P.; Prettyman, T.; Lestone, J.

    1998-01-01

    The authors have used a tomographic gamma scanner (TGS) to produce tomographic prompt gamma-ray neutron activation analysis imaging (PGNAA) of heterogeneous matrices. The TGS was modified by the addition of graphite reflectors that contain isotopic neutron sources for sample interrogation. The authors are in the process of developing the analysis methodology necessary for a quantitative assay of large containers of heterogeneous material. This nondestructive analysis (NDA) technique can be used for material characterization and the determination of neutron assay correction factors. The most difficult question to be answered is the determination of the source-to-sample coupling term. To assist in the determination of the coupling term, the authors have obtained images for a range of sample that are very well characterized, such as, homogenous pseudo one-dimensional samples to three-dimensional heterogeneous samples. They then compare the measurements to MCNP calculations. For an accurate quantitative measurement, it is also necessary to determine the sample gamma-ray self attenuation at higher gamma-ray energies, namely pair production should be incorporated into the analysis codes

  19. Neutron emission from impacted solid LiD samples

    International Nuclear Information System (INIS)

    Kaushik, T.C.; Shyam, A.; Kulkarni, L.V.; Srinivasan, M.

    1993-01-01

    Nylon projectiles with 0.1 g to 0.3 g mass, accelerated to velocities of 0.2-1 km/s using a 60 cm long electromagnetic accelerator (railgun), have been impacted upon solid lithium deuteride (LiD) samples of 3 proportional counters. The output from the BF 3 set-up is monitored in several ways to characterize the possible neutron emission from the target. This includes a simple technique of counting the single channel analyser (SCA) output through a dead-time unit to identify bursts of < 100 μs duration. Counting is started after a delay of ∼ 1 ms to avoid the initial interference from the capacitor bank discharge. The signal is also recorded in a storage oscilloscope from the start of projectile acceleration along with a time marker just before the impact. From a number of shots taken with and without the samples, a significant evidence of neutron emission from the LiD samples appears to emerge. The experiments suggest that approximately 100 neutrons might be generated during every such impact in a duration of < 4 ms. (author). 7 refs., 3 figs

  20. Elemental Study in Soybean and Products by Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Vorapot, Permnamtip; Arporn Busamongkol; Sirinart, Laoharojanaphand

    2009-07-01

    Full text: Elements were analyzed in soybean and products by Instrumental Neutron Activation Analysis (INAA), Pseudo-Cyclic Instrumental Neutron Activation Analysis (PCINAA) and Epithermal Instrumental Neutron Activation Analysis (EINAA). Elements detected in sample were include Al, Br, Ca, Cl, Cu, Fe, I, K, Mg, Mn Na, Se and Zn. The result showed that the nutritional contents changed after food processing. From experiments (n = 2), it was found that after food processing, the concentration of Cl and Na in soy bean curd increased from 0.0045 and 0.0011% to found 0.91 and 0.39 %, respectively. Other elements did not differ from soybean. Limits of detection for Al, Br, Ca, Cl, Cu, Fe, I, K, Mg, Mn Na, Se and Zn were 0.05, 0.2, 50, 6, 10, 15, 0.05, 30, 40, 5, 5, 0.05 and 1 mg.kg - 1, respectively

  1. Physical basis for prompt-neutron activation analysis

    International Nuclear Information System (INIS)

    Chrien, R.E.

    1982-01-01

    The technique called prompt ν-ray neutron activation analysis has been applied to rapid materials analysis. The radiation following the neutron radiation capture is prompt in the sense that the nuclear decay time is on the order of 10 - 15 second, and thus the technique is not strictly activation, but should be called radiation neutron capture spectroscopy or neutron capture ν-ray spectroscopy. This paper reviews the following: sources and detectors, theory of radiative capture, nonstatistical capture, giant dipole resonance, fast neutron capture, and thermal neutron capture ν-ray spectra. 14 figures

  2. Determination of arsenic and bromine in hot spring waters by neutron activation analysis

    International Nuclear Information System (INIS)

    Kikawada, Y.; Kawai, S.; Oi, T.

    2004-01-01

    Concentrations of arsenic and bromine dissolved in hot spring waters have been determined by neutron activation analysis using 0.5 cm 3 of sample waters without any chemical pretreatment. The samples prepared for neutron irradiation were simply pieces of filter papers which were infiltrated with samples. With the results of satisfactorily high accuracy and precision, this analytical method was found to be very convenient for the determinations of arsenic and bromine dissolved in water at ppm to sub-ppm levels. (author)

  3. Comparison of laser fluorimetry, high resolution gamma-ray spectrometry and neutron activation analysis techniques for determination of uranium content in soil samples

    International Nuclear Information System (INIS)

    Ghods, A.; Asgharizadeh, F.; Salimi, B.; Abbasi, A.

    2004-01-01

    Much more concern is given nowadays for exposure of the world population to natural radiation especially to uranium since 57% of that exposure is due to radon-222, which is a member of uranium decay series. Most of the methods used for uranium determination is low concentration require either tedious separation and preconcentration or the accessibility to special instrumentation for detection of uranium at this low level. this study compares three techniques and methods for uranium analysis among different soil sample with variable uranium contents. Two of these techniques, neutron activation analysis and high resolution gamma-ray spectrometry , are non-destructive while the other, laser fluorimetry is done via chemical extraction of uranium. Analysis of standard materials is done also to control the quality and accuracy of the work. In spite of having quite variable ranges of detection limit, results obtained by high resolution gamma-ray spectrometry based on the assumption of having secular equilibrium between uranium and its daughters, which causes deviation whenever this condition was missed. For samples with reasonable uranium content, neutron activation analysis would be a rapid and reliable technique, while for low uranium content laser fluorimetry would be the most appropriate and accurate technique

  4. Determination of the sodium, aluminium, potassium, manganese, magnesium, bromine, cadmium and chlorine concentration values in the whole blood samples of human cancer using neutron activation analysis facility of the second Egyptian research reactor

    Directory of Open Access Journals (Sweden)

    N. F. Soliman

    2010-06-01

    Full Text Available Neutron activation analysis (NAA using the Second Egyptian Research Reactor (ETRR-2 has been utilized to analyze whole blood samples. The National Cancer Institute of Egypt provided us with 18 blood samples (11 breast, 2 prostate, 2 colon, 1 pancreatic, 1 ovarian and a random sample of normal person to estimate the concentration values of Sodium, Aluminium, Potassium, Manganese, Magnesium, Bromine, Chlorine. The pneumatic irradiation rabbit system (PIRS built in the vertical thermal column of the ETRR-2 reactor is used for short time irradiation at constant power. Elemental concentrations were estimated from measurements of the gamma-ray spectra of the product short lived isotopes in the samples. The calculated thermal to epithermal neutron flux ratio was found to be 196 at irradiation position. The tabulated concentrations were calculated by using k0-neutron activation analysis (k0NAA standardization method.

  5. Determination of oxygen content in steel using activation analysis with 14 MeV neutron

    International Nuclear Information System (INIS)

    Calado, C.E.

    1978-01-01

    In the quantitative analysis of oxygen in steel by fast neutron activation analysis the oxygen content is evaluated from the measured activity of 16 N produced. Steel s mples are irradiated in 14 MeV neutron flux. After irradiation the samples are pneumatically transfered to the counting terminal where activity is measured. Oxygen concentrations, are obtained by comparison with standards of specified oxygen content [pt

  6. A neutron activation analyzer

    International Nuclear Information System (INIS)

    Westphal, G.P.; Lemmel, H.; Grass, F.; De Regge, P.P.; Burns, K.; Markowicz, A.

    2005-01-01

    Dubbed 'Analyzer' because of its simplicity, a neutron activation analysis facility for short-lived isomeric transitions is based on a low-cost rabbit system and an adaptive digital filter which are controlled by a software performing irradiation control, loss-free gamma-spectrometry, spectra evaluation, nuclide identification and calculation of concentrations in a fully automatic flow of operations. Designed for TRIGA reactors and constructed from inexpensive plastic tubing and an aluminum in-core part, the rabbit system features samples of 5 ml and 10 ml with sample separation at 150 ms and 200 ms transport time or 25 ml samples without separation at a transport time of 300 ms. By automatically adapting shaping times to pulse intervals the preloaded digital filter gives best throughput at best resolution up to input counting rates of 10 6 cps. Loss-free counting enables quantitative correction of counting losses of up to 99%. As a test of system reproducibility in sample separation geometry, K, Cl, Mn, Mg, Ca, Sc, and V have been determined in various reference materials at excellent agreement with consensus values. (author)

  7. Measuring neutron yield and ρR anisotropies with activation foils at the National Ignition Facility

    Directory of Open Access Journals (Sweden)

    Bleuel D.L.

    2013-11-01

    Full Text Available Neutron yields at the National Ignition Facility (NIF are measured with a suite of diagnostics, including activation of ∼20–200 g samples of materials undergoing a variety of energy-dependent neutron reactions. Indium samples were mounted on the end of a Diagnostic Instrument Manipulator (DIM, 25–50 cm from the implosion, to measure 2.45 MeV D-D fusion neutron yield. The 336.2 keV gamma rays from the 4.5 hour isomer of 115mIn produced by (n,n′ reactions are counted in high-purity germanium detectors. For capsules producing D-T fusion reactions, zirconium and copper are activated via (n,2n reactions at various locations around the target chamber and bay, measuring the 14 MeV neutron yield to accuracies on order of 7%. By mounting zirconium samples on ports at nine locations around the NIF chamber, anisotropies in the primary neutron emission due to fuel areal density asymmetries can be measured to a relative precision of 3%.

  8. Measurement of mercury isotopic ratio in stone meteorites by neutron activation analysis

    International Nuclear Information System (INIS)

    Thakur, A.N.

    1997-01-01

    196 Hg and 202 Hg isotopes have been measured by neutron activation analysis in samples of twelve stone meteorites. Hg is extracted from an irradiated sample by stepwise heating. The mercury concentrations vary from 0.07 to 33 ppm. While most of the samples give 196 Hg/ 202 Hg ratios similar to terrestrial value within error limits, in some cases large anomalies are observed. A number of control experiments have been devised, that show the absence of experimental artifacts, during sample preparation, neutron irradiation, chemical separation and counting stages. Several anomalous and normal Hg distillate have been re-irradiated as Hg-diethyl-dithio-carbamate complex to eliminate the influence of neutron self shielding and interfering reactions from matrix elements. The isotopic ratio patterns persist in the distillates too proving that any artifacts during meteorite irradiation and measurement are essentially absent. Both positive and negative anomalies are observed: however, the negative anomalies are much more frequent and abundant. In an extreme case of fine grained magnetic particles of Ambapur Nagla the 196 Hg is apparently absent in the Hg released at 100 deg C. A 2σ 196 Hg/ 202 Hg value is only 6% relative to the monitor. This experiment shows the robustness of neutron activation analysis and suggest some constrains on the formation history of stone meteorites. (author)

  9. The determination of some impurities in zirconium metal by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Eddy, B.T.; Pearton, D.C.G.; Watterson, J.J.

    1976-01-01

    This report describes the work done on the development of an instrumental neutron-activation method for the analysis of impurities in reactor-grade zirconium. Nine samples were analysed, and the results were compared with those obtained by other techniques. No statistically significant differences were observed for ten of the twelve elements that could possibly be determined by instrumental neutron-activation analysis. Cadmium cannot be determined at the 0,5 p.p.m. level, and there is doubt about the comparative values recorded for aluminium. The precision of the measurement by direct instrumental neutron-activation analysis ranges from 1,4 per cent for tungsten to 17 per cent for chromium [af

  10. Determination of silver, gold, zinc and copper in mineral samples by various techniques of instrumental neutron activation analysis; Determinacion de plata, oro, zinc y cobre en muestras minerales mediante diversas tecnicas de analisis por activacion de neutrones instrumental

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez R, N. I.; Rios M, C.; Pinedo V, J. L. [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas, Zac. (Mexico); Yoho, M.; Landsberger, S., E-mail: neisla126@hotmail.com [University of Texas at Austin, Nuclear Engineering Teaching Laboratory, Austin 78712, Texas (United States)

    2015-09-15

    Using the method of instrumental neutron activation analysis, mineral exploration samples were analyzed in order to determine the concentrations of silver, gold, zinc and copper; these minerals being the main products of benefit of Tizapa and Cozamin mines. Samples were subjected to various techniques, where the type of radiation and counting methods were chosen based on the specific isotopic characteristics of each element. For calibration and determination of concentrations the comparator method was used, certified standards were subjected to the same conditions of irradiation and measurement that the prospecting samples. The irradiations were performed at the research reactor TRIGA Mark II of the University of Texas at Austin. The silver concentrations were determined by Cyclical Epithermal Neutron Activation Analysis. This method in combination with the transfer pneumatic system allowed a good analytical precision and accuracy in prospecting for silver, from photo peak measurement 657.7 keV of short half-life radionuclide {sup 110}Ag. For the determination of gold and zinc, Epithermal Neutron Activation Analysis was used, the photo peaks analyzed corresponded to the energies 411.8 keV of radionuclide {sup 199}Au and 438.6 keV of metastable radionuclide {sup 69m}Zn. On the other hand, copper quantification was based on the photo peak analysis of 1039.2 keV produced by the short half-life radionuclide {sup 66}Cu, by Thermal Neutron Activation Analysis. The photo peaks measurement corresponding to gold, zinc and copper was performed using a Compton suppression system, which allowed an improvement in the signal to noise relationship, so that better detection limits and low uncertainties associated with the results were obtained. Comparing elemental concentrations the highest values in silver, zinc and copper was for samples of mine Tizapa. Regarding gold values were found in the same range for both mines. To evaluate the precision and accuracy of the methods used

  11. Determination of the hydrogen content of oil samples from Nigeria using an Am-Be neutron source

    International Nuclear Information System (INIS)

    Jonah, S.A.; Elegba, S.B.; Zakari, I.I.

    1998-01-01

    A 5 Ci Am-Be neutron source-based facility, which utilises the principles of thermal neutron reflection technique in combination with foil activation method, has been used to determine the total hydrogen content of commercial oil samples from Nigeria. With an established detection limit of 0.25 H w% for oil matrix of volume 600-ml, the total hydrogen contents of the samples were found to be in the range of 11.11-14.22 H w%. The facility is economical and suitable for the determination of moisture in solid samples. A brief description of the ongoing projects and future plans concerning the CRP are enumerated. (author)

  12. Trace elements in coloured opals using neutron activation analysis

    International Nuclear Information System (INIS)

    McOrist, G.D.; Smallwood, A.

    1995-01-01

    Neutron activation analysis was used to determine the concentration of trace elements in 50 samples of orange, yellow, honey, green, blue and pink opals as well as 18 samples of colourless opals taken from a number of recognised fields in Australia, Peru, Mexico and USA. The results were evaluated to determine the relationship between trace elements content and opal colour. (author). 10 refs., 10 figs., 3 tabs

  13. Workbook on reactor neutron activation analysis (NAA) of airborne particulate matter (APM)

    International Nuclear Information System (INIS)

    Tian Weizhi

    2000-01-01

    This publication presents general aspects of reactor neutron activation analysis (NAA) applied to measurement of elemental composition of airborne particulate matter. It presents an introduction to the NAA, its' basic principles and brief history of the method and discusses its' advantages and disadvantages. This publication also presents experimental procedures of NAA including sampling and sample preparation; preparation of calibration standard samples; reactor neutron irradiation; gamma-spectroscopy of the irradiated samples; quantification and presentation of analytical results. The publication pays attention to the quality assurance and quality control procedures including internal quality control, analysis of certified reference materials, and interlaboratory and multi-method comparison studies, control charts

  14. Multi-group transport methods for high-resolution neutron activation analysis

    International Nuclear Information System (INIS)

    Burns, K. A.; Smith, L. E.; Gesh, C. J.; Shaver, M. W.

    2009-01-01

    The accurate and efficient simulation of coupled neutron-photon problems is necessary for several important radiation detection applications. Examples include the detection of nuclear threats concealed in cargo containers and prompt gamma neutron activation analysis for nondestructive determination of elemental composition of unknown samples. In these applications, high-resolution gamma-ray spectrometers are used to preserve as much information as possible about the emitted photon flux, which consists of both continuum and characteristic gamma rays with discrete energies. Monte Carlo transport is the most commonly used modeling tool for this type of problem, but computational times for many problems can be prohibitive. This work explores the use of multi-group deterministic methods for the simulation of neutron activation problems. Central to this work is the development of a method for generating multi-group neutron-photon cross-sections in a way that separates the discrete and continuum photon emissions so that the key signatures in neutron activation analysis (i.e., the characteristic line energies) are preserved. The mechanics of the cross-section preparation method are described and contrasted with standard neutron-gamma cross-section sets. These custom cross-sections are then applied to several benchmark problems. Multi-group results for neutron and photon flux are compared to MCNP results. Finally, calculated responses of high-resolution spectrometers are compared. Preliminary findings show promising results when compared to MCNP. A detailed discussion of the potential benefits and shortcomings of the multi-group-based approach, in terms of accuracy, and computational efficiency, is provided. (authors)

  15. Bromine and iodine in Chinese medical herbs determined via epithermal neutron activation analysis

    International Nuclear Information System (INIS)

    Chien-Yi Chen; Yuan-Yaw Wei; Sheng-Pin ChangLai; Lung-Kwang Pan

    2003-01-01

    Nineteen natural herbs and two prescriptions prepared from mixed herbs were analyzed via epithermal neutron activation analysis (ENAA) to evaluate their bromine and iodine concentration. Traditional medical doctors prescribed the samples presented in this work to most Taiwanese children for strengthening their immune systems. Empirical results indicated a wide diversity of bromine in the samples. Yet, the iodine concentration was only around one to tenth or twentieth of the bromine. The maximum daily intake (MDI) for various medical herbs was also widely diversified from one to tenfold on the basis of various criteria. The minimum detectable concentration (MDC) of bromine and iodine found was 0.42±0.14 ppm and 0.067±0.016 ppm, respectively. Compared to that from conventional thermal neutron activation analysis (NAA) for a similar evaluation, the extremely low MDC obtained here was attributed to the large amount of thermal neutron absorption during sample irradiation. (author)

  16. Neutron Activation Analysis with k0-standardisation

    International Nuclear Information System (INIS)

    Pomme, S.

    2001-01-01

    SCK-CEN's programme on Neutron Activation Analysis with k 0 -standardisation concentrates on the improvement of the standardisation method and the characterisation of the neutron field as well as on the improvement of the statistical control on neutron activation analysis. Main achievements in 2000 are reported

  17. Preconcentration method using an activatable yield tracer for neutron activation analysis

    International Nuclear Information System (INIS)

    Tsukada, Masamichi; Yamamoto, Daijiro; Endo, Kazutoyo; Nakahara, Hiromichi

    1991-01-01

    Previously, the use of an enriched stable isotope as an activatable yield tracer in preconcentration steps has been tested by use of commercially available enriched 116 Cd and 156 Dy for biological standard reference materials. In the present work, this method has been further applied to the determination of lanthanoid contents in various kinds of samples: one coal fly-ash, three Japanese standard rocks, and eight standard soils. Samples were decomposed by alkali fusion in the preconcentration step. Thirteen elements were determined for coal fly-ash and soil samples, and 14 elements for rocks. The data obtained for coal fly-ash and standard rocks are compared with the data reported in literature. The data for soil samples have been newly determined in the present work. The ordinary instrumental neutron activation analysis and radiochemical neutron activation analysis were also performed to confirm the accuracy and usefulness of the present method. (author) 10 refs.; 4 tabs

  18. The Comparison Study of Neutron Activation Analysis and Fission Track Technique for Uranium Determination

    International Nuclear Information System (INIS)

    Sirinuntavid, Alice; Rodthongkom, Chouvana

    2007-08-01

    Full text: Comparison between Neutron Activation Analysis (NAA) and fission track technique for uranium determination in solid samples was studied by use of standard reference materials, i.e., ore, coal fly ash, soil. For NAA, the epithermal neutron was applied for activated irradiation. Then, the 74.5 keV gamma from U-239 or 277.7 keV gamma from Np-239 was measured. For high Uranium content samples, NAA method with 74.5 keV gamma measurement, gave higher precision result than the 277.7 keV gamma measurement method. NAA method with 277.7 keV gamma measurement, gave higher sensitivity and precision result for low Uranium content samples and the uranium contained less than 10 ppm samples. Nevertheless, the latter procedure needed longer time for neutron irradiation and analysis procedure. In comparison the results of Uranium analysis between NAA and fission track, it was found that no significant difference within 95 % of confidence level

  19. Determination of molybdenum and selenium in bioenvironmental samples using neutron activation analysis

    International Nuclear Information System (INIS)

    Abu-Samra, A.; Morris, J.S.; Koirtyohann, S.R.; Vogt, J.R.

    1974-01-01

    Because of the increasing interest as to their roles in biological systems, a procedure has been developed by which molybdenum and selenium can be determined at nanogram levels in these types of samples. Results from the analysis of orchard leaves and bovine liver are presented. The samples are packaged in pre-cleaned quartz vials prepared from GE-204 tubing. If both selenium and molybdenum are to be determined, the samples are irradiated for 40 or more hours at a thermal neutron flux of 8 x 10 13 n cm -2 sec -1 . After the samples have decayed for approximately 48 hours the vials are unpackaged, cleaned in aqua-regia, and broken. The irradiation period can be reduced to 24 hours if molybdenum is to be determined individually or if the selenium content is known to be 1 microgram or more. The sample is digested with carriers and the selenium is then distilled as a volatile selenium halide. Elemental selenium is precipitated by reduction with SO 2 produced through the protonation of the hydrogen sulfite ion and subsequent decomposition of the resulting sulfurous acid. The 401 keV summation peak of 75 Se is normally used for quantitative determination. The chemical yield is determined by drying and weighing the elemental selenium

  20. Neutron activation analysis of absolutely-dated tree rings

    International Nuclear Information System (INIS)

    Uenlue, K.; Hauck, D.K.; Kuniholm, P.I.; Chiment, J.J.

    2005-01-01

    Gold concentration was determined for dendrochronologically-dated wood samples using neutron activation analysis (NAA) and correlation sought with known environmental changes, e.g., volcanic activities, during historic periods. Uptake of gold is sensitive to soil pH for many plants. Data presented are from a single, cross-dated tree that grew in Greece. Using NAA, gold was measured with parts-per-billion sensitivity in individual tree rings from 1411 to 1988 AD. (author)

  1. The synchronous active neutron detection assay system

    International Nuclear Information System (INIS)

    Pickrell, M.M.; Kendall, P.K.

    1994-01-01

    We have begun to develop a novel technique for active neutron assay of fissile material in spent nuclear fuel. This approach will exploit a 14-MeV neutron generator developed by Schlumberger. The technique, termed synchronous active neutron detection (SAND), follows a method used routinely in other branches of physics to detect very small signals in presence of large backgrounds. Synchronous detection instruments are widely available commercially and are termed ''lock-in'' amplifiers. We have implemented a digital lock-in amplifier in conjunction with the Schlumberger neutron generator to explore the possibility of synchronous detection with active neutrons. The Schlumberger system can operate at up to a 50% duty factor, in effect, a square wave of neutron yield. Results are preliminary but promising. The system is capable of resolving the fissile material contained in a small fraction of the fuel rods in a cold fuel assembly; it also appears resilient to background neutron interference. The interrogating neutrons appear to be non-thermal and penetrating. Work remains to fully explore relevant physics and optimize instrument design

  2. Applied research of environmental monitoring using instrumental neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Chung, Young Sam; Moon, Jong Hwa; Chung, Young Ju

    1997-08-01

    This technical report is written as a guide book for applied research of environmental monitoring using Instrumental Neutron Activation Analysis. The contents are as followings; sampling and sample preparation as a airborne particulate matter, analytical methodologies, data evaluation and interpretation, basic statistical methods of data analysis applied in environmental pollution studies. (author). 23 refs., 7 tabs., 9 figs.

  3. Thermal neutron detection by activation of CaSO4:Dy + KBr thermoluminescent phosphors

    International Nuclear Information System (INIS)

    Gordon, A.M.P.L.; Muccillo, R.

    1979-01-01

    Thermoluminescence (TL) studies to detect thermal neutrons were performed in cold-pressed CaSO 4 :0,1%Dy + KBr samples. The detection is based on the self-irradiation of the CaSO 4 :Dy TL phosphor by the Br isotopes activated by exposure to a mixed neutron-gamma field. (Author) [pt

  4. Application of neutron activation analysis for mercury species determination in scalp hair samples from Malaysia, Libya and Jordan

    International Nuclear Information System (INIS)

    Sarmani, S.B.; Alakili, I.

    2004-01-01

    Neutron activation analysis was used to determine the levels of total mercury and methylmercury in hair samples obtained from 400 Malaysian (Kuala Lumpur), Libyan (Benghazi) and Jordanian (Amman) donors. Results show that the level of total mercury in hair samples of the Malaysian group (3.38 mg x kg -1 ) was significantly higher than those of Libyan (0.81 mg x kg -1 ) and Jordanian groups (0.69 mg x kg -1 ). Likewise, a significant difference was found between the level of methylmercury of the Malaysian group (1.13 mg x kg -1 ) and those of the Libyan (0.04 mg x kg -1 ) and Jordanian groups (0.13 mg x kg -1 ). This difference could be attributed to the variation in life habits especially fish diet and to the local environment of each population. On the other hand, no significant differences were found between the level of total mercury and methylmercury in hair samples of the Libyan and Jordanian residents. (author)

  5. Reactor neutron activation analysis for aluminium in the presence of phosphorus and silicon

    International Nuclear Information System (INIS)

    Mizumoto, Yoshihiko; Iwata, Shiro; Sasajima, Kazuhisa; Yoshimasu, Fumio; Yase, Yoshiro.

    1984-01-01

    Reactor neutron activation analysis for aluminium in samples containing phosphorus and silicon was studied. The experiments were performed by using neumatic tube of the Kyoto University Reactor (KUR). At first, the ratios of the 28 Al activity produced from 27 Al(n, γ) 28 Al reaction by thermal neutrons to that from 31 P(n, α) 28 Al reaction by fast neutrons, and to that from 28 Si(n, p) 28 Al reaction were measured by γ-ray spectrometry. With a ratio of about 5 for the thermal to fast neutron flux of KUR, the ratio of the 28 Al activity from aluminium to that from phosphorus was to be 812 +- 7, and to that from silicon 282 +- 3. Secondly, the contributions of 28 Al activities from phosphorus and silicon and the determination limit of aluminium were calculated for various parameters, such as fast neutron flux, thermal to fast neutron flux ratio, amounts of phosphorus and silicon, etc. Thirdly, on the basis of these results, aluminium contents in spinal cords and brains of amyotrophic lateral sclerosis, Parkinsonism-dementia complex and control cases were determined. (author)

  6. Neutron activation analysis with pulsed 14 MeV neutrons for the characterization of heterogeneous radioactive wastes; Neutronenaktivierungsanalyse mit gepulsten 14 MeV Neutronen zur Charakterisierung heterogener radioaktiver Abfaelle

    Energy Technology Data Exchange (ETDEWEB)

    Mildenberger, Frank

    2017-07-01

    For the transport, interim storage and disposal of radioactive waste, it is assumed to have knowledge of the radioactive and non-radioactive inventory. In order to determine the radioactive inventory destructive (e.g. α-, β-, γ-measurements according to wet chemical sample preparation) and non-destructive (e.g. γ-scanning and neutron measurements) measurement methods are used. For the characterization of non-radioactive substances a prototype for the assay of small-volume (50 L) samples was constructed and parameterized using the neutron activation analysis (NAA) with a pulsed 14 MeV neutron source. Subsequently, the non-destructive analytical method called MEDINA (Multi Element Detection Based on Instrumental Neutron Activation) for 200 l waste drums was developed in a cooperation between RWTH Aachen University and Forschungszentrum Juelich GmbH. The aim of this thesis is to investigate and characterize heterogeneous mixed samples regarding their material composition as well as their inhomogeneous distribution. For this purposes, studies were carried out on 200 l steel drums with heterogeneous matrices using the NAA in the MEDINA facility. The samples are composed out of a mixture of concrete and polyethylene (PE) bodies. Due to its high hydrogen content, the PE can have a strong influence on the neutron moderation and neutron absorption and can thereby occur as a possible disturbance variable in the characterization of the non-radioactive inventory. For these studies a pulsed 14 MeV neutron source is used to record the prompt and delayed γ-rays between the neutron pulses, separately. Thus, the performance of the MEDINA method relating to strongly moderating mixed matrices and their characterization is studied. In order to optimize the measurement of delayed γ-rays without any appreciable interference of prompt γ-rays, the decay of thermal neutrons was studied and the thermal neutron die-away time was determined. It ranges between 2 and 5 ms according to

  7. Uncertainties in measuring trace amounts of cobalt and europium with low-flux neutron activation analysis

    Directory of Open Access Journals (Sweden)

    Burnham Steven

    2017-01-01

    Full Text Available Neutron activation analysis is widely used for identification of elements and their quantities even in trace amounts in the samples of almost any type. The challenges in detecting trace amounts of particular elements are often associated with the neutron flux produced at the research reactors. Low-flux neutron activation analysis usually presents the biggest challenge when analyzing trace quantities of elements with lower magnitude of radiative capture cross-sections. In this paper, we present the methodology and the quantified uncertainties associated with the detection of trace amounts of cobalt and europium, using as an example concrete aggregates. Recent growing interest is in improving structural concrete (increasing its strength but reducing its activation in nuclear power plant environments. Aside from buildings, structural concrete is also used as a biological shield in nuclear power plant that become radioactive after exposure to neutron flux. Due to radiative capture interactions, artificial radionuclides are generated to high enough concentrations that classify concrete as low-level radioactive waste at the time of the plant's decommissioning. Disposal of this concrete adds to the expense of nuclear power plant financing and its construction. Three radionuclides, 60Co, 152Eu, and 154Eu, account for 99 % of total residual radioactivity of nuclear power plant decommissioned concrete. IAEA document RS-G-1.7, Application of the Concepts of Exclusion, Exemption, and Clearance, specifies clearance levels of radionuclides specific activities: a specific activity lower than 0.1 Bqg-1 for 60Co and 152Eu, and 154Eu allows for a concrete to be recycled after decommissioning of the nuclear power plant. Therefore, low-flux neutron activation analysis is used to test the detection limits of trace elements in samples of cement, coarse, and fine concrete aggregates. These samples are irradiated at the University of Utah's 100 kW TRIGA Reactor at

  8. Imaging of heterogeneous materials by prompt gamma-ray neutron activation analysis

    International Nuclear Information System (INIS)

    Staples, Parrish; Prettyman, Tom; Lestone, John

    1999-01-01

    We have used a Tomographic Gamma Scanner (TGS) to produce tomographic Prompt Gamma-Ray Neutron Activation Imaging of heterogeneous matrices [T.H. Prettyman, R.J. Estep, G.A. Sheppard, Trans. Am. Nucl. Soc. 69 (1993) 183-184]. The TGS was modified by the addition of graphite reflectors that contain isotopic neutron sources for sample interrogation. We are in the process of developing the analysis methodology necessary for a quantitative assay of large containers of heterogeneous material. This nondestructive analysis technique can be used for material characterization and the determination of neutron assay correction factors. The most difficult question to be answered is the determination of the source to sample coupling term. To assist in the determination of the coupling term we have obtained images for a range of samples that are very well characterized; such as, homogenous pseudo one-dimensional samples to three-dimensional heterogeneous samples. We then compare the measurements to Monte Carlo N-particle calculations. For an accurate quantitative measurement it is also necessary to determine the sample gamma-ray self attenuation at higher gamma-ray energies, namely pair production should be incorporated into the analysis codes

  9. Use of research reactors for neutron activation analysis. Report of an advisory group meeting

    International Nuclear Information System (INIS)

    2001-04-01

    and to provide assistance through the IAEA in identifying fields of application where neutron activation analysis can be of enhanced value to countries. In view of the above, it is recommended that Member States promote the use of neutron activation analysis using their low and medium flux reactors. The focus should be on: (1) Reduction of the total analysis time by developing neutron activation analysis based on short lived radionuclides; (2) Development of optimised analysis protocols. Use of larger sample quantities to compensate for low neutron fluxes and to reduce counting times; (3) Use of neutron activation analysis for validation of other methods of elemental analysis; (4) Feasibility studies for samples related to industrial production, such as fossil fuels, mining, food, agricultural products, and waste management and recycling; (5) Optimization of neutron beam quality for prompt gamma neutron activation analysis, which provides additional elements and/or may result in reduction of analysis time. Close co-operation between experienced neutron activation analysis laboratories and new or inexperienced facilities associated with research reactors is highly desirable. From the experience accumulated to date on the usage of reactors for neutron activation analysis in Canada, China, Jamaica and elsewhere, it is concluded that low flux research reactors are a good choice for developing countries wishing to embark on neutron activation analysis

  10. DETERMINATION OF LIMIT DETECTION OF THE ELEMENTS N, P, K, Si, Al, Fe, Cu, Cd, WITH FAST NEUTRON ACTIVATION USING NEUTRON GENERATOR

    Directory of Open Access Journals (Sweden)

    Sunardi Sunardi

    2010-06-01

    Full Text Available Determination of limit detection of the elements N, P, K, Si, Al, Fe, Cu, Cd, with fast neutron activation using neutron generator has been done.  Samples prepared from SRM 2704, N, P, K elements from MERCK, Cu, Cd, Al from activation foil made in San Carlos, weighted and packed for certain weight then iradiated during 30 minutes with 14 MeV fast neutron using the neutron generator and then counted with gamma spectrometry (accuspec.  At this research condition of neutron generator was set at current 1 mA that produced neutron flux about 5,47.107 n/cm2.s and  experimental result shown that the limit detection for the elements N, P, K, Si, Al, Fe, Cu, Cd are  2,44 ppm, 1,88 ppm, 2,15 ppm, 1,44 ppm, 1,26 ppm, 1,35 ppm, 1,05 ppm, 2,99 ppm, respectively.  The data  indicate that the limit detection or sensitivity of appliance of neutron generator to analyze the element is very good, which is feasible to get accreditation AANC laboratory using neutron generator.   Keywords: limit detection, AANC, neutron generator

  11. Progress report on neutron activation analysis at Dalat Nuclear Research Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Tuan, Nguyen Ngoc [Nuclear Research Institute, Dalat (Viet Nam)

    2003-03-01

    Neutron Activation Analysis (NAA) is one of most powerful techniques for the simultaneous multi-elements analysis. This technique has been studied and applied to analyze major, minor and trace elements in Geological, Biological and Environmental samples at Dalat Nuclear Research Reactor. At the sixth Workshop, February 8-11, 1999, Yojakarta, Indonesia we had a report on Current Status of Neutron Activation Analysis using Dalat Nuclear Research Reactor. Another report on Neutron Activation Analysis at the Dalat Nuclear Research Reactor also was presented at the seventh Workshop in Taejon, Korea from November 20-24, 2000. So in this report, we would like to present the results obtained of the application of NAA at NRI for one year as follows: (1) Determination of the concentrations of noble, rare earth, uranium, thorium and other elements in Geological samples according to requirement of clients particularly the geologists, who want to find out the mineral resources. (2) The analysis of concentration of radionuclides and nutrient elements in foodstuffs to attend the program on Asian Reference Man. (3) The evaluation of the contents of trace elements in crude oil and basement rock samples to determine original source of the oil. (4) Determination of the elemental composition of airborne particle in the Ho Chi Minh City for studying air pollution. The analytical data of standard reference material, toxic elements and natural radionuclides in seawater are also presented. (author)

  12. Progress report on neutron activation analysis at Dalat Nuclear Research Reactor

    International Nuclear Information System (INIS)

    Tuan, Nguyen Ngoc

    2003-01-01

    Neutron Activation Analysis (NAA) is one of most powerful techniques for the simultaneous multi-elements analysis. This technique has been studied and applied to analyze major, minor and trace elements in Geological, Biological and Environmental samples at Dalat Nuclear Research Reactor. At the sixth Workshop, February 8-11, 1999, Yojakarta, Indonesia we had a report on Current Status of Neutron Activation Analysis using Dalat Nuclear Research Reactor. Another report on Neutron Activation Analysis at the Dalat Nuclear Research Reactor also was presented at the seventh Workshop in Taejon, Korea from November 20-24, 2000. So in this report, we would like to present the results obtained of the application of NAA at NRI for one year as follows: (1) Determination of the concentrations of noble, rare earth, uranium, thorium and other elements in Geological samples according to requirement of clients particularly the geologists, who want to find out the mineral resources. (2) The analysis of concentration of radionuclides and nutrient elements in foodstuffs to attend the program on Asian Reference Man. (3) The evaluation of the contents of trace elements in crude oil and basement rock samples to determine original source of the oil. (4) Determination of the elemental composition of airborne particle in the Ho Chi Minh City for studying air pollution. The analytical data of standard reference material, toxic elements and natural radionuclides in seawater are also presented. (author)

  13. Neutron activation analysis of trace elements in rain water

    International Nuclear Information System (INIS)

    Luten, J.B.

    1977-01-01

    In this thesis the principles and practical aspects of activation analysis which are of direct importance in the analysis of rain water, are presented together with recent literature data on other techniques. Problems due to the storage of rain water samples are discussed. A multi-element method for the determination of trace elements in rain water by instrumental neutron activation analysis is described. Gamma ray spectrometry using Ge(Li) detectors offers the possibility to determine Na, Al, Cl, V, Mn, Co, Cu, Br and I in rain water samples of 2.5 ml after a 4-min irradiation in a thermal neutron flux of 5 x 10 13 n cm -2 s -1 . In residues of rain water samples of 100 ml, irradiated during 2 days in a thermal neutron flux of >5 x 10 13 n cm -2 s -1 Cr, Fe, Co, Zn and Sb can be determined after a cooling period of approximately 21 days. The detection limits are lower than those reported in previous investigations except for Cu. The precision is about 10% or better, except for Co, Cu and I. A routine method for the determination of bromine and iodine in rain water by n.a.a. is presented. The elements are isolated by isotope exchange between the irradiated sample and a solution of Br 2 or I 2 in CCl 4 . The method is not sensitive to the chemical species in which the halogen is present. Irradiation of solutions of iodine compounds in a high thermal neutron flux gives rise to the formation of iodate. Results of a further investigation of this phenomenon are given, as well as the determination of iodate in rain water by n.a.a. Iodate is separated by anion exchange. The combination of n.a.a. and solvent extraction is used for the determination of five trace elements (V, Co, Cu, Zn and In) in 10-ml rain water samples. For V, Co and Cu this method is more sensitive and reproducible than instrumental n.a.a. The results of the analysis of eleven sequential 30-ml samples from the beginning of the shower are presented as an illustration of possible applications of the

  14. Sampling and analytical methodologies for instrumental neutron activation analysis of airborne particulate matter

    International Nuclear Information System (INIS)

    1992-01-01

    The IAEA supports a number of projects having to do with the analysis of airborne particulate matter by nuclear techniques. Most of this work involves the use of activation analysis in its various forms, particularly instrumental neutron activation analysis (INAA). This technique has been widely used in many different countries for the analysis of airborne particulate matter, and there are already many publications in scientific journals, books and reports describing such work. The present document represents an attempt to summarize the most important features of INAA as applied to the analysis of airborne particulate matter. It is intended to serve as a set of guidelines for use by participants in the IAEA's own programmes, and other scientists, who are not yet fully experienced in the application of INAA to airborne particulate samples, and who wish either to make a start on using this technique or to improve their existing procedures. The methodologies for sampling described in this document are of rather general applicability, although they are presented here in a way that takes account of the particular requirements arising from the use of INAA as the analytical technique. The analytical part of the document, however, is presented in a form that is applicable only to INAA. (Subsequent publications in this series are expected to deal specifically with other nuclear related techniques such as energy dispersive X ray fluorescence (ED-XRF) and particle induced X ray emission (PIXE) analysis). Although the methods and procedures described here have been found through experience to yield acceptable results, they should not be considered mandatory. Any other procedure used should, however, be chosen to be capable of yielding results at least of equal quality to those described

  15. Sampling and analytical methodologies for instrumental neutron activation analysis of airborne particulate matter

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1992-12-01

    The IAEA supports a number of projects having to do with the analysis of airborne particulate matter by nuclear techniques. Most of this work involves the use of activation analysis in its various forms, particularly instrumental neutron activation analysis (INAA). This technique has been widely used in many different countries for the analysis of airborne particulate matter, and there are already many publications in scientific journals, books and reports describing such work. The present document represents an attempt to summarize the most important features of INAA as applied to the analysis of airborne particulate matter. It is intended to serve as a set of guidelines for use by participants in the IAEA's own programmes, and other scientists, who are not yet fully experienced in the application of INAA to airborne particulate samples, and who wish either to make a start on using this technique or to improve their existing procedures. The methodologies for sampling described in this document are of rather general applicability, although they are presented here in a way that takes account of the particular requirements arising from the use of INAA as the analytical technique. The analytical part of the document, however, is presented in a form that is applicable only to INAA. (Subsequent publications in this series are expected to deal specifically with other nuclear related techniques such as energy dispersive X ray fluorescence (ED-XRF) and particle induced X ray emission (PIXE) analysis). Although the methods and procedures described here have been found through experience to yield acceptable results, they should not be considered mandatory. Any other procedure used should, however, be chosen to be capable of yielding results at least of equal quality to those described.

  16. Neutron activation analysis of alternative waste forms at the Savannah River Laboratory

    International Nuclear Information System (INIS)

    Johns, R.A.

    1981-01-01

    A remotely controlled system for neutron activation of candidate high-level waste (HLW) isolation forms was built by the Savannah River Laboratory at a Savannah River Plant reactor. With this system, samples can be irradiated for up to 24 hours and transferred through pneumatic tubing to a shielded repository unitl their activity is low enough for them to be handled in a radiobench. The principal use of the system is to support the Alternative Waste Forms Leach Testing (AWFLT) Program in which the comparative leachability of the various waste forms will be determined. The experimental method used in this work is based on neutron activation analysis techniques. Neutron irradiation of the solid waste form containing simulated HLW sludge activates elements in the sample. After suitable leaching of the solid matrix in standard solutions, the leachate and solid are assayed for gamma-emitting nuclides. From these measurements, the fraction of a specific element leached can be determined al half-lives with experimental ones, over a range of 24 orders of magnitude was obtained. This is a strong argument that the alpha decay could be considered a fission process with very high mass asymmetry and charge density asymmetry

  17. Self-absorption of neutron capture gamma-rays in gold samples

    International Nuclear Information System (INIS)

    Wisshak, K.; Walter, G.; Kaeppeler, F.

    1983-06-01

    The self absorption of neutron capture gamma rays in gold samples has been determined experimentally for two standard setups used in measurements of neutron capture cross sections. One makes use of an artificially collimated neutron beam and two C 6 D 6 detectors, the other of kinematically collimated neutrons and three Moxon-Rae detectors. Correction factors for an actual measurement of a neutron capture cross section using a gold standard of 1 mm thickness up to 12% were found for the first setup while they are only 4% for the second setup. The present data allow to determine the correction in an actual measurement with an accuracy of 0.5-1%. (orig.) [de

  18. Determination of selenium in BCR single cell protein via destructive neutron activation analysis

    International Nuclear Information System (INIS)

    Goeij, J.J.M. de; Zegers, C.

    1978-10-01

    The amount of selenium 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 1.0 x 10 13 n/cm 2 s for 24 hours. After chemical destruction of the samples the amount of selenium was determined by measuring the γ-peaks of selenium-75

  19. Transmission of 14 MeV neutrons through concrete, soil, sugar, wood and coal samples - a Monte Carlo Study

    International Nuclear Information System (INIS)

    Abdelmonem, M.S.; Naqvi, A.A.

    2006-01-01

    Full text: Fast neutrons transmission measurements are ideal for the elemental analysis of bulk samples. In particular, they can be used to determine the hydrogen concentration in bulk samples. In the present study, Monte Carlo simulations have been carried to calculate the intensity of 14 MeV neutrons transmitted through concrete, soil, sugar, wood and coal samples. The simulated set-up consists of a cylindrical sample, placed at a distance of 9 cm from the neutron source. Fast neutrons transmitted through the sample are collimated through a double truncated neutron collimator to a fast neutron detector. The collimator contains a mixture of paraffin and lithium carbonate. In this study, transmitted intensity of fast neutron through each sample was calculated as a function of moisture contents of the sample for 14 MeV neutrons. The moisture contents of the samples were varied over 0-7 wt. %. The calculated intensity of 14 MeV neutrons transmitted through the samples, shows effects related to fast neutron thermalization in hydrogen of moisture and energy dependence of neutron transmission through the sample materials. This is clearly shown by different gradients of neutron yield vs moisture content curves of these samples. The gradient of the neutron yield curves for the 14 MeV neutrons has a lower value than those reported for a 241 Am-Be neutron source

  20. Activation of cobalt by neutrons from the Hiroshima bomb

    International Nuclear Information System (INIS)

    Kerr, G.D.; Dyer, F.F.; Emery, J.F.; Pace, J.V. III; Brodzinski, R.L.; Marcum, J.

    1990-02-01

    A study has been completed of cobalt activation in samples from two new locations in Hiroshima. The samples consisted of a piece of steel from a bridge located at a distance of about 1300 m from the hypocenter and pieces of both steel and concrete from a building located at approximately 700 m. The concrete was analyzed to obtain information needed to calculate the cobalt activation in the two steel samples. Close agreement was found between calculated and measured values for cobalt activation of the steel sample from the building at 700 m. It was found, however, that the measured values for the bridge sample at 1300 m were approximately twice the calculated values. Thus, the new results confirm the existence of a systematic error in the transport calculations for neutrons from the Hiroshima bomb. 52 refs., 32 figs., 16 tabs

  1. Accurate measurements of neutron activation cross sections

    International Nuclear Information System (INIS)

    Semkova, V.

    1999-01-01

    The applications of some recent achievements of neutron activation method on high intensity neutron sources are considered from the view point of associated errors of cross sections data for neutron induced reaction. The important corrections in -y-spectrometry insuring precise determination of the induced radioactivity, methods for accurate determination of the energy and flux density of neutrons, produced by different sources, and investigations of deuterium beam composition are considered as factors determining the precision of the experimental data. The influence of the ion beam composition on the mean energy of neutrons has been investigated by measurement of the energy of neutrons induced by different magnetically analysed deuterium ion groups. Zr/Nb method for experimental determination of the neutron energy in the 13-15 MeV energy range allows to measure energy of neutrons from D-T reaction with uncertainty of 50 keV. Flux density spectra from D(d,n) E d = 9.53 MeV and Be(d,n) E d = 9.72 MeV are measured by PHRS and foil activation method. Future applications of the activation method on NG-12 are discussed. (author)

  2. High sensitivity neutron activation analysis of environmental and biological standard reference materials

    International Nuclear Information System (INIS)

    Greenberg, R.R.; Fleming, R.F.; Zeisler, R.

    1984-01-01

    Neutron activation analysis is a sensitive method with unique capabilities for the analysis of environmental and biological samples. Since it is based upon the nuclear properties of the elements, it does not suffer from many of the chemical effects that plague other methods of analysis. Analyses can be performed either with no chemical treatment of the sample (instrumentally), or with separations of the elements of interest after neutron irradiation (radiochemically). Typical examples of both types of analysis are discussed, and data obtained for a number of environmental and biological SRMs are presented. (author)

  3. A neutron multiplicity analysis method for uranium samples with liquid scintillators

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Hao, E-mail: zhouhao_ciae@126.com [China Institute of Atomic Energy, P.O.BOX 275-8, Beijing 102413 (China); Lin, Hongtao [Xi' an Reasearch Institute of High-tech, Xi' an, Shaanxi 710025 (China); Liu, Guorong; Li, Jinghuai; Liang, Qinglei; Zhao, Yonggang [China Institute of Atomic Energy, P.O.BOX 275-8, Beijing 102413 (China)

    2015-10-11

    A new neutron multiplicity analysis method for uranium samples with liquid scintillators is introduced. An active well-type fast neutron multiplicity counter has been built, which consists of four BC501A liquid scintillators, a n/γdiscrimination module MPD-4, a multi-stop time to digital convertor MCS6A, and two Am–Li sources. A mathematical model is built to symbolize the detection processes of fission neutrons. Based on this model, equations in the form of R=F*P*Q*T could be achieved, where F indicates the induced fission rate by interrogation sources, P indicates the transfer matrix determined by multiplication process, Q indicates the transfer matrix determined by detection efficiency, T indicates the transfer matrix determined by signal recording process and crosstalk in the counter. Unknown parameters about the item are determined by the solutions of the equations. A {sup 252}Cf source and some low enriched uranium items have been measured. The feasibility of the method is proven by its application to the data analysis of the experiments.

  4. Determination of fluorine in fodder phosphates and phosphorite flour by fast neutron activation method

    International Nuclear Information System (INIS)

    Abashin, E.G.; Lisovskij, I.P.; Smakhtin, L.A.

    1980-01-01

    A neutron-activation method is suggested for determination of fluorine in fodder phosphates and phosphorite flour. Used as the source of fast neutrons was an NG-150M neutron generator with a maximum yield of 10 8 nxcm -2 xs -1 . Samples were irradiated in polyethylene ampoules using a pneumatic shuttle. Fluorine was determined with reference to the fluorine-18 isotope. The accuracy of determining fluorine in fodder phosphates and phosphorite flour is 1 to 4% (rel.) at a rate of not less than 10 samples per hour. The method is suitable for in-process testing of products

  5. Determination of fluorine in fodder phosphates and phosphorite flour by fast neutron activation method

    Energy Technology Data Exchange (ETDEWEB)

    Abashin, E G; Lisovskii, I P; Smakhtin, L A

    1980-01-01

    A neutron-activation method is suggested for determination of fluorine in fodder phosphates and phosphorite flour. Used as the source of fast neutrons was an NG-150M neutron generator with a maximum yield of 10/sup 8/ nxcm/sup -2/xs/sup -1/. Samples were irradiated in polyethylene ampoules using a pneumatic shuttle. Fluorine was determined with reference to the fluorine-18 isotope. The accuracy of determining fluorine in fodder phosphates and phosphorite flour is 1 to 4% (rel.) at a rate of not less than 10 samples per hour. The method is suitable for in-process testing of products.

  6. Neutron activation analysis using Excel files and Canberra Genie-2000

    International Nuclear Information System (INIS)

    Landsberger, S.; Jackman, K.; Welch, L.

    2005-01-01

    A method for analyzing neutron activated sample data by using Microsoft Excel as the analysis engine has been developed. A simple technique for inputting data is based on report files generated by Canberra's Genie-2000 spectroscopy system but could be easily modified to support other vendors having report formats with consistent text placement. A batch program handles operating an automatic sample changer, acquiring the data, and analyzing the spectrum to create a report of the peak locations and net area. The entire report is then transferred to within an Excel spreadsheet as the source data for neutron activation analysis. Unique Excel templates have been designed, for example, to accommodate short-lived and long-lived isotopes. This process provides a largely integrated solution to NAA while providing the results in an industry standard spreadsheet format. This software is ideally suited for teaching and training purposes. (author)

  7. Neutron activation analysis for calibration of phosphorus implantation dose

    International Nuclear Information System (INIS)

    Paul, Rick L.; Simons, David S.

    2001-01-01

    A feasibility study was undertaken to determine if radiochemical neutron activation analysis (RNAA) can be used to certify the retained dose of phosphorus implanted in silicon, with the goal of producing a phosphorus SRM. Six pieces of silicon, implanted with a nominal phosphorus dose of 8.5x10 14 atoms·cm -2 were irradiated at a neutron flux of 1.05x10 14 cm -2 ·s -1 . The samples were mixed with carrier, dissolved in acid, the phosphorus isolated by chemical separation, and 32 P measured using a beta proportional counter. A mean phosphorus concentration of (8.35±0.20)x10 14 atoms·cm -2 (uncertainty=1 standard deviation) was determined for the six samples, in agreement with the nominal implanted dose

  8. Pollution of agricultural crops with lanthanides, thorium and uranium studied by instrumental and radiochemical neutron activation analysis

    International Nuclear Information System (INIS)

    Kucera, J.; Mizera, J.; Randa, Z.; Vavrova, M.

    2007-01-01

    The lanthanide elements, Th and U were measured in soils and agricultural crops collected in an area polluted by emissions from a phosphate fertilizer plant. Concentrations of the above elements in the soil and crop samples were determined by instrumental neutron activation analysis (INAA). Selected crop samples were also analyzed using radiochemical neutron activation analysis (RNAA) based on alkaline-oxidative fusion of the irradiated samples followed by precipitation of REE oxalates. Elevated levels of lanthanides, Th and U were found in some samples, especially in wheat chaff and parsley. (author)

  9. Neutron activation: an invaluable technique for teaching applied radiation

    International Nuclear Information System (INIS)

    Trainer, Matthew

    2002-01-01

    This experiment introduces students to the important method of neutron activation. A sample of aluminium was irradiated with neutrons from an isotropic 241 Am-Be source. Using γ-ray spectroscopy, two radionuclide products were identified as 27 Mg and 28 Al. Applying a cadmium cut-off filter and an optimum irradiation time of 45 min, the half-life of 27 Mg was determined as 9.46±0.50 min. The half-life of the 28 Al radionuclide was determined as 2.28±0.10 min using a polythene moderator and an optimum irradiation time of 10 min. (author)

  10. Absolute instrumental neutron activation analysis at Lawrence Livermore Laboratory

    International Nuclear Information System (INIS)

    Heft, R.E.

    1977-01-01

    The Environmental Science Division at Lawrence Livermore Laboratory has in use a system of absolute Instrumental Neutron Activation Analysis (INAA). Basically, absolute INAA is dependent upon the absolute measurement of the disintegration rates of the nuclides produced by neutron capture. From such disintegration rate data, the amount of the target element present in the irradiated sample is calculated by dividing the observed disintegration rate for each nuclide by the expected value for the disintegration rate per microgram of the target element that produced the nuclide. In absolute INAA, the expected value for disintegration rate per microgram is calculated from nuclear parameters and from measured values of both thermal and epithermal neutron fluxes which were present during irradiation. Absolute INAA does not depend on the concurrent irradiation of elemental standards but does depend on the values for thermal and epithermal neutron capture cross-sections for the target nuclides. A description of the analytical method is presented

  11. Neutron activation analysis in reconnaissance geochemical survey of Northwestern Mindoro

    International Nuclear Information System (INIS)

    Santos, G. Jr.; Fernandez, L.G.

    1987-01-01

    Instrumental neutron activation analysis (NAA) technique was used to analyze stream sediments collected in Northwestern Mindoro. The concentration levels of 18 elements were determined. It was noted that NAA is suitable for the determination of rare earth, gold, arsenic and cobalt among others because of favorable high neutron cross sections. Samples collected in regional reconnaissance geochemical surveys could be analyzed usng NAA technique to complement other non-nuclear techniques, such as atomic absorption and X-ray fluorescence analysis. (Author). 11 figs.; 2 tabs.; 12 refs

  12. Instrumental Neutron Activation Analysis for Human Hair

    International Nuclear Information System (INIS)

    Ratanatongchai, W.; Dharmvanij, W; Chongkum, S.

    1998-01-01

    Hair samples from students aged between 7 to 22 years old were analysed by neutron activation analysis at nuclear research reactor TRR-1.M1. From qualitative analysis of short-lived isotopes, A1, V, Ca, I, Cl, Mn, and Na were found. The quantity of those elements can be classified into three groups. The first group is A1, Ca, Na and Cl with variance less than 10%. The second group is V and I with variance between 10% to 50% and the third group, Mn, two samples have concentration about 12 times higher than the others

  13. Design considerations for neutron activation and neutron source strength monitors for ITER

    International Nuclear Information System (INIS)

    Barnes, C.W.; Jassby, D.L.; LeMunyan, G.; Roquemore, A.L.

    1997-01-01

    The International Thermonuclear Experimental Reactor will require highly accurate measurements of fusion power production in time, space, and energy. Spectrometers in the neutron camera could do it all, but experience has taught us that multiple methods with redundancy and complementary uncertainties are needed. Previously, conceptual designs have been presented for time-integrated neutron activation and time-dependent neutron source strength monitors, both of which will be important parts of the integrated suite of neutron diagnostics for this purpose. The primary goals of the neutron activation system are: to maintain a robust relative measure of fusion energy production with stability and wide dynamic range; to enable an accurate absolute calibration of fusion power using neutronic techniques as successfully demonstrated on JET and TFTR; and to provide a flexible system for materials testing. The greatest difficulty is that the irradiation locations need to be close to plasma with a wide field of view. The routing of the pneumatic system is difficult because of minimum radius of curvature requirements and because of the careful need for containment of the tritium and activated air. The neutron source strength system needs to provide real-time source strength vs. time with ∼1 ms resolution and wide dynamic range in a robust and reliable manner with the capability to be absolutely calibrated by in-situ neutron sources as done on TFTR, JT-60U, and JET. In this paper a more detailed look at the expected neutron flux field around ITER is folded into a more complete design of the fission chamber system

  14. Toroidal deuteron accelerator for Mo-98 neutron activation

    Energy Technology Data Exchange (ETDEWEB)

    Araujo, Wagner L., E-mail: wagner.leite@ifnmg.edu.br, E-mail: tprcampos@pq.cnpq.br [Instituto Federal do Norte de Minas Gerais (IFN-MG), Montes Claros, MG (Brazil); Campos, Tarcisio P.R. Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Departamento de Engenharia Nuclear

    2017-07-01

    The radionuclide Tc-{sup 99m} is the most useful radioisotope in nuclear medicine. It can be produced by the Mo-99 beta minus decay. Mo-99 has often been produced in a high- flux nuclear reactor through radioactive neutron capture reactions on Mo-98. The present paper provides a preliminary design of a toroidal transmutation system (TTS) based on a toroidal compact deuteron accelerator, which can provide the Mo-98 transmutation into Mo-99. This system is essentially composed of a multi-aperture plasma electrode and a target, submitted to 180 kV, where a positive deuteron beam is accelerated toward a titanium-target loaded with deuterium in which nuclear d-d fusion reactions are induced. The Particle Studio package of the Computer Simulation Technology (CST) software was applied to design, simulate and optimize the deuteron beam on the target. MCNP code provided to neutronic analysis. Based on electromagnetic and neutronic simulations, the neutron yield and reaction rates were estimated. The simulated data allowed appraising the Mo-99 activity. A TTS, in a specific configuration, could produce a total deuterium current of 1.6 A at the target and a neutron yield of 10{sup 13} n.s{sup -1}. In a arrangement of 30 column samples, TTS provides 230 mCi s{sup -1} Mo{sup 99} in each column, which represents 80% of Tc-99m in secular equilibrium. As conclusion, the system holds potential for generating Mo-99 and Tc-99m in a suitable activity in secular equilibrium. (author)

  15. Toroidal deuteron accelerator for Mo-98 neutron activation

    International Nuclear Information System (INIS)

    Araujo, Wagner L.; Campos, Tarcisio P.R. Universidade Federal de Minas Gerais

    2017-01-01

    The radionuclide Tc- 99m is the most useful radioisotope in nuclear medicine. It can be produced by the Mo-99 beta minus decay. Mo-99 has often been produced in a high- flux nuclear reactor through radioactive neutron capture reactions on Mo-98. The present paper provides a preliminary design of a toroidal transmutation system (TTS) based on a toroidal compact deuteron accelerator, which can provide the Mo-98 transmutation into Mo-99. This system is essentially composed of a multi-aperture plasma electrode and a target, submitted to 180 kV, where a positive deuteron beam is accelerated toward a titanium-target loaded with deuterium in which nuclear d-d fusion reactions are induced. The Particle Studio package of the Computer Simulation Technology (CST) software was applied to design, simulate and optimize the deuteron beam on the target. MCNP code provided to neutronic analysis. Based on electromagnetic and neutronic simulations, the neutron yield and reaction rates were estimated. The simulated data allowed appraising the Mo-99 activity. A TTS, in a specific configuration, could produce a total deuterium current of 1.6 A at the target and a neutron yield of 10 13 n.s -1 . In a arrangement of 30 column samples, TTS provides 230 mCi s -1 Mo 99 in each column, which represents 80% of Tc-99m in secular equilibrium. As conclusion, the system holds potential for generating Mo-99 and Tc-99m in a suitable activity in secular equilibrium. (author)

  16. Fast neutron activation analysis using short-lived radionuclides

    International Nuclear Information System (INIS)

    Salma, I.; Zemplen-Papp, E.

    1993-01-01

    Fast neutron activation analysis experiments were performed to investigate the analytical possibilities and prospective utilization of short-lived activation products. A rapid pneumatic transfer system for use with neutron generators has been installed and applied for detecting radionuclides with a half-life from ∼300 ms to 20 s. The transport time for samples of total mass of 1-4 g is between 130 and 160 ms for pressurized air of 0.1-0.4 MPa. The reproducibility of transport times is less than 2%. The employed method of correcting time-dependent counting losses is based on the virtual pulse generator principle. The measuring equipment consists of CAMAC modules and a special gating circuit. Typical time distributions of counting losses are presented. The same 14 elements were studied by the conventional activation method (single irradiation and single counting) by both a typical pneumatic transport system (run time 3 s) and the fast pneumatic transport facility. Furthermore, the influence of the cyclic activation technique on the elemental sensitivities was investigated. (author) 15 refs.; 5 figs.; 3 tabs

  17. A Brief overview of neutron activation analyses methodology and applications

    International Nuclear Information System (INIS)

    Ali, M.A.

    2000-01-01

    The primary objective of this talk is to present our new facility for Neutron Activation Analysis to the scientific and industrial societies and show its possibilities. Therefore my talk will handle the following main items: An overview of neutron activation analysis, The special interest of fast mono-energetic neutrons, The NAA method and its sensitivities, The Recent scientific and industrial applications using NAA, and o An illustrating example measured by using our facility is presented What is NAA? It is a sensitive analytical technique useful for performing both qualitative and quantitative multi-element analyses in samples. Worldwide application of NAA is so widespread; it is estimated that approximately several 10,000 samples undergo analysis each year from almost every conceivable field of scientific or technical interest. Why NAA? For many elements and applications, NAA: Offers sensitivities that are sometimes superior to those attainable by other methods, on the order of nano-gram level, It is accurate and reliable, NAA is generally recognized as the r eferee method o f choice when new procedures are being developed or when other methods yield results that do not agree. However, the activation analysis at En=14 MeV is limited by a few factors: Low value of flux, low cross-sections of threshold reactions, o Short irradiation time due to finite target life, Interfering reactions and gamma ray spectral interference

  18. Rapid radiochemical separation of short-lived radionuclides in neutron-activated samples

    International Nuclear Information System (INIS)

    Fardy, J.

    1985-11-01

    Radiochemical separation procedures based on the removal of metal ions by columns of C 18 -bonded silica gel after selective complexation are examined and the simplicity of the method demonstrated by its application to determination of Mn, Cu and Zn in neutron-activated biological material from the following solutions (pH 0-10, sulphate concentration 0,18M and 1,44M SO 4 ): 8-hydroxyquinoline (oxine), ammonium pyrrolidinedithiocarbamate (APDC), cupferron (CUP), 1-(2-pyridylazo)-2-naphthol (PAN), 1-(2'-thiazolylazo)-2-naphthol (TAN), 4-(2-pyridylazo) resorcinol (PAR), diethylammonium diethyldithiocarbamate (DDC), potassium ethyl xanthate (PEX), acetylacetone (AcAc) or thenoyltrifluoracetone (TTA). The method is rapid and reliable and readily adaptable in all radiochemical laboratories

  19. Pulse neutron logging technique

    International Nuclear Information System (INIS)

    Bespalov, D.F.; Dylyuk, A.A.

    1975-01-01

    A new method of neutron-burst logging is proposed, residing in irradiating rocks with fast neutron bursts and registering the integrated flux burst of thermal and/or epithermal neutrons, from the moment of its initiation to that of full absorption. The obtaained value is representative of the rock properties (porosity, hydrogen content). The integrated flux in a burst of thermal and epithermal neutrons can be measured both by way of activation of a reference sample of a known chemical composition during the neutron burst and by recording the radiation of induced activity of the sample within an interval between two bursts. The proposed method features high informative value, accuracy and efficiency

  20. Multielement neutron-activation analysis of plants and fertilizers

    International Nuclear Information System (INIS)

    Srapenyants, R.A.; Saveliev, I.B.

    1977-01-01

    The development of an automated technique for simultaneous multielement activation analysis of plants and fertilizers for the macronutrient elements N, P, K, Ca, Mg, Cl, and Si is presented. The developed universal NAA is based on the installation manufactured and supplied by Sames, France. The components of the automatic installation for neutron activation analysis are: neutron generator; a pneumatic transfer system; a scintillation crystal detector; a spectrometer rack including a basic multichannel analyser; a control panel for the neutron generator and pneumatic transfer system; a computer and teletype. On the basis of analytical procedures, algorithms and software, the first automatic (computer based) installation for multielement analyses of plants and fertilizers has been completed and is in routine use in the agrochemical and plant breeding research program in the Soviet Union. The proposed technique together with the full automatic real-time process of measurement and processing of data by computer, provides a throughput of 250-500 samples (1250-2500 elements determinations) per 8-hour shift, with the accuracy of +-3%; for N and +-5%; for P, K, Mg, Cl and +-15% for Ca. (T.G.)

  1. Thermal neutron absorption cross section of small samples

    International Nuclear Information System (INIS)

    Nghiep, T.D.; Vinh, T.T.; Son, N.N.; Vuong, T.V.; Hung, N.T.

    1989-01-01

    A modified steady method for determining the macroscopic thermal neutron absorption cross section of small samples 500 cm 3 in volume is described. The method uses a moderating block of paraffin, Pu-Be neutron source emitting 1.1x10 6 n.s. -1 , SNM-14 counter and ordinary counting equipment. The interval of cross section from 2.6 to 1.3x10 4 (10 -3 cm 2 g -1 ) was measured. The experimental data are described by calculation formulae. 7 refs.; 4 figs

  2. Trace elements in Australian opals using neutron activation analysis

    International Nuclear Information System (INIS)

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

    1994-01-01

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

  3. Proceedings of national seminar neutron activation analysis

    International Nuclear Information System (INIS)

    Agus Taftazani; Muhayatun Santoso; Budi Haryanto; Khatarina Oginawati

    2010-11-01

    Proceedings of national seminar neutron activation analysis in 2010 with the theme of the Role of Nuclear Analytical Techniques in the Field of Environment, Health and Industry. The seminar was organized by Indonesians Neutron Activation Analysis and BATAN Forum. These proceedings contain the result of environmental research in BATAN, universities and institutions associated with the application on neutron activation analysis technique. The purpose of these proceedings was as a useful source of information to spur research and development of activation analysis applications in various fields for the Indonesian welfare. There are 40 articles. (PPIKSN).

  4. The Prompt Gamma Neutron Activation Analysis Facility at ICN-Pitesti

    International Nuclear Information System (INIS)

    Barbos, D.; Paunoiu, C.; Mladin, M.; Cosma, C.

    2008-01-01

    PGNAA is a very widely applicable technique for determining the presence and amount of many elements simultaneously in samples ranging in size from micrograms to many grams. PGNAA is characterized by its capability for nondestructive multi-elemental analysis and its ability to analyse elements that cannot be determined by INAA. By means of this PGNAA method we are able to increase the performance of INAA method. A facility has been developed at Institute for Nuclear Research-Pitesti so that the unique features of prompt gamma-ray neutron activation analysis can be used to measure trace and major elements in samples. The facility is linked at the radial neutron beam tube at ACPR-TRIGA reactor. During the PGNAA-facility is in use the ACPR reactor will be operated in steady-state mode at 250 KW maximum power. The facility consists of a radial beam-port, external sample position with shielding, and induced prompt gamma-ray counting system.Thermal neutron flux with energy lower than cadmium cut-off at the sample position was measured using thin gold foil is: φ scd = 1.10 6 n/cm 2 /s with a cadmium ratio of:80.The gamma-ray detection system consist of an HpGe detector of 16% efficiency (detector model GC1518) with 1.85 keV resolution capability. The HpGe is mounted with its axis at 90 deg. with respect to the incident neutron beam at distance about 200mm from the sample position. To establish the performance capabilities of the facility, irradiation of pure element or sample compound standards were performed to identify the gama-ray energies from each element and their count rates

  5. Sample handling and chemical procedures for efficacious trace analysis of urine by neutron activation analysis

    International Nuclear Information System (INIS)

    Blotcky, A.J.; Rack, E.P.; Roman, F.R.

    1988-01-01

    Important for the determination of trace elements, ions, or compounds in urine by chemical neutron activation analysis is the optimization of sample handling, preirradiation chemistry, and radioassay procedures necessary for viable analysis. Each element, because of its natural abundance in the earth's crust and, hence, its potential for reagent and environmental contamination, requires specific procedures for storage, handling, and preirradiation chemistry. Radioassay techniques for radionuclides vary depending on their half-lives and decay characteristics. Described in this paper are optimized procedures for aluminum and selenium. While 28 Al (T 1/2 = 2.24 min) and 77m Se(T 1/2 = 17.4s) have short half-lives, their gamma-ray spectra are quite different. Aluminum-28 decays by a 1779-keV gamma and 77m Se by a 162-keV gamma. Unlike selenium, aluminum is a ubiquitous element in the environment requiring special handling to minimize contamination in all phases of its analytical determination

  6. Errors in instumental neutron activation analysis caused by matrix absorption

    International Nuclear Information System (INIS)

    Croudace, I.W.

    1979-01-01

    Instrumental neutron activation analysis of the geochemically important rare earth elements, together with Ta, Hf and U involves energies below 150 keV where absorption of radiation by the sample becomes inceasingly important. Determinations of the total mass absorption coefficients have been made. (C.F.)

  7. International intercomparison of fluence of fast neutrons using 115In(n,γ) activation

    International Nuclear Information System (INIS)

    Lesiecki, H.; Cosack, M.

    1985-07-01

    The Physikalisch-Technische Bundesanstalt (PTB) has participated in an international intercomparison of fluence measurements of fast neutrons. This was organized under the auspices of the ''Comite Consultatif pour les Etalons de Mesure des Rayonnements Ionisants (CCEMRI)'', Sect. 3 (Mesures Neutronique). The National Physical Laboratory (NPL), Teddington, UK volunteered to assume responsibility for the experimental realization and final evaluation. This report deals with the measurements performed at the PTB for the neutron fluence intercomparison at neutron energies of Esub(n) = 144 keV and 570 keV which was based on the 115 In(n,γ) 116 Insup(m) reaction. The count rate of a 4πβ-counter which had to be used to determine the activation of the In sample was to be compared with the neutron fluence by which the sample was irradiated. A description of the neutron production, the fluence determination, the 4πβ-counting, and the evaluation of the results will be given. (orig.) [de

  8. Determination of arsenic, selenium and antimony by neutron activation analysis. Application to hair samples

    International Nuclear Information System (INIS)

    Das, H.A.; Hoede, D.; Nieuwendijk, B.J.T.; Sloot, H.A. van der; Teunissen, G.J.A.; Woittiez, J.R.W.

    1983-04-01

    A fast rabbit system for instrumental activation analysis with reactor neutrons is described. Its use in the determination of selenium in hair is discussed. A survey is given of the correction factors which are inherent to the use of short-lived radionuclides. An alternative to INAA is NAA based on the separation of arsenic, selenium and antimony by hydride evaporation and adsorption to active carbon. Data for some Standard Reference Materials are given. This work was done under research contract 2440/RI/RB with the IAEA

  9. Use of neutron activation and X-ray fluorescence with radioactive sources (Cf-252 and Am-241) for the instrumental qualiquantitative simultaneous analysis of some elements in samples of mineral supplement for animals

    International Nuclear Information System (INIS)

    Simabuco, S.M.

    1984-01-01

    To study the possibility of using two non-destructive (neutron activation and X-ray fluorescence) analyses in simultaneous quali-quantitative evaluations of some elements in mineral supplement for animals, a Cf-252 neutron source (11.3 mCi; 21.1 μgrams) and a Am-241 low energy gamma-ray emitter source (59.5 KeV; 100 mCi) were employed. For these sources, shieldings and sample irradiation systems were built. For the neutron activation analysis a reservoir of 72 cm height and 43 cm diameter was filled with paraffine, and the samples and neutron sources were put inside this reservoir using polypropilene and nylon tubes. To detect the gamma-rays emitted by the radioisotopes a well-type solid NaI(Tl) crystal scintillator (3x3') was used, coupled to a multi-channel analyser. For the X-ray fluorescence analysis a lead cylinder of 9.75 cm height and 5.6 cm diameter (with 0.7 cm thickness) was made and internally lined with a 0.36 mm copper and 0.1 mm aluminium foil. (Author) [pt

  10. Reactor neutron activation for multielemental analysis

    International Nuclear Information System (INIS)

    Reddy, A.V.R.

    1999-01-01

    activation analysis is applied to determine the concentration of REEs in quartzites and other minerals from the Cuddapah basin to understand the REE patterns and mineralogical processes. A comprehensive programme of analysing air, water and soil samples around the mining area is under progress to obtain the correlations between the environmental load with toxic elements and possible health implications vis-a-vis human beings and plant materials. Elemental concentrations of a few varieties of cereals, pulses and leaves were measured. The obtained values were utilised to examine the role of major and minor elements in terms of dietary and curative value of these leaves, cereals and pulses. Trace elements in the leaves could be determined more reliably using radiochemical neutron activation by separating the bulk elements like Na, K and Br, with enhanced sensitivity. A programme to determine nutrient elements and their availability for the plants through soil and water, and nature of species present is initiated. In each set of the experiments, the precision and accuracy were evaluated by determining the concentration of the elements in standard materials. In the studies of minerals USGS standard reference materials AGV-1 and W-1, for nodules and crusts NOD-A-1, for sediments SOIL-7 and for leaves SRM-1571 were analysed along with the samples of interest. CNAA and RNAA were applied for trace element analysis of the SOIL-7 and SRM-1571. (author)

  11. Determination of the total amount of organically bound chlorine, bromine and iodine in environmental samples by instrumental neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Gether, J; Lunde, G [Central Institute for Industrial Research, Oslo (Norway); Steinnes, E [Institutt for Atomenergi, Kjeller (Norway)

    1979-07-01

    The determination of chlorine, bromine and iodine present as non-polar, hydrophobic hydrocarbons in environmental samples is reported. The organohalogen compounds are seprated from water into an organic phase by on-site liquid-liquid extraction, and form biological material by procedures based on lipid phase extraction and codistillation. After removal of inorganic halides by washing with water and concentration of the sample by evaporation of the solvent, the resulting extracts are analyzed for their chlorine, bromine and iodine contents by instrumental neutron activation analysus. Strict attention is paid to the possibility of contamination in every step of the procedure. Background values in routine analysis are approximately 100-200 ng of chlorine, <5 ng of bromine and <3 ng of iodine.

  12. Californium-252 neutron activation analysis of high-level processed nuclear tank waste

    International Nuclear Information System (INIS)

    Troyer, G.L.; Purcell, M.A.

    2000-01-01

    The basis for production assessment of the vitrification of Hanford nuclear fuel reprocessing wastes will be high-precision measurements of the elemental sodium content. However, the chemical analysis of both radioactive and nonradioactive components in nuclear waste can be challenged by high radiation dose rates. The dose rates compromise many analytical techniques as well as pose personnel dosimetry risks. In many cases, reduction of dose rates through dilution compromises the precision and sensitivity for certain key components. The use of neutron activation analysis (NAA) provides a method of analysis that avoids the need for dilutions or extensive sample preparation. These waste materials also contain trace quantities of fissionable isotopes, which, through neutron activation, can be estimated by delayed neutron counting of fissioned fragments

  13. Neutron activation analysis applied to nutritional and foodstuff studies

    International Nuclear Information System (INIS)

    Maihara, Vera A.; Santos, Paola S.; Moura, Patricia L.C.; Castro, Lilian P. de; Avegliano, Roseane P.

    2009-01-01

    Neutron Activation Analysis, NAA, has been successfully used on a regularly basis in several areas of nutrition and foodstuffs. NAA has become an important and useful research tool due to the methodology's advantages. These include high accuracy, small quantities of samples and no chemical treatment. This technique allows the determination of important elements directly related to human health. NAA also provides data concerning essential and toxic concentrations in foodstuffs and specific diets. In this paper some studies in the area of nutrition which have been carried out at the Neutron Activation Laboratory of IPEN/CNEN-SP will be presented: a Brazilian total diet study: nutritional element dietary intakes of Sao Paulo state population; a study of trace element in maternal milk and the determination of essential trace elements in some edible mushrooms. (author)

  14. Activation analysis with neutron generators using short-lived radionuclides

    International Nuclear Information System (INIS)

    Salma, I.

    1993-01-01

    The short half-life involves a number of important differences in production, transportation and measurement of radionuclides, and in counting statistics as compared with those in traditional activation analysis. Experiments were performed to investigate the analytical possibilities and prospective utilization of short-lived radionuclides produced by 14-MeV neutron irradiation. A rapid pneumatic transfer system for use with neutron generators was installed and applied for detecting radionuclides with a half-life from 300 ms to 30 s. The transport time for samples with a total mass of 1-4 g is between 130 and 160 ms for pressurized air of 0.1-0.4 MPa. 11 elements were studied by the conventional activation method using both a typical pneumatic transport system (run time 3 s) and the fast pneumatic transport facility. The effect of the cyclic activation technique on the elemental sensitivities was also investigated. (orig.)

  15. Application of neutron activation analysis to the determination of minor-and trace elements in magnesite ore

    International Nuclear Information System (INIS)

    Sepulveda Munita, C.J.A.; Atalla, L.T.

    1979-01-01

    A method employing analysis with thermal neutrons was developed for analyzing magnesite samples coming from the States do Ceara and Bahia (Brazil). Ten samples were analyzed. Qualitative analysis of the samples indicated the presence of Mn, Fe, Sc, Ca, Cu, Co and some of the lanthanides. Mn was analyzed by non-destructive activation analysis and the other elements were analyzed, individually or in group, after sample dissolution with 8 N HCl solution. A detailed study of the possible interferences in neutron activation analysis of the elements considered was also undertaken. The precision and accuracy of the results obtained and the sensitivity of the method are discussed. (Author) [pt

  16. Fast neutron activation analysis in metallurgy

    International Nuclear Information System (INIS)

    Sterlinski, S.

    1981-01-01

    Article discusses the usage of a 14 MeV neutron generator for producing fast neutrons of different energies and intensities. A complete instrumental set-up for the neutron activation analysis (NAA) is given. In metallurgy the device is mainly used in the determination of oxygen and silicon in steel and non-ferrous metal, including different alloys

  17. Neutron activation analysis and activity in the vessel steel of a BWR reactor for their study without radiological risks in microscopy and spectrometry

    International Nuclear Information System (INIS)

    Moranchel, M.; Garcia B, A.; Longoria G, L. C.

    2012-01-01

    The vessel material of nuclear reactors is subject to irradiation damage induced by the bombardment of neutrons coming from the reactor core. Neutrons are classified as fast and thermal, which produce different effects. Fast neutrons cause damage to the material by dislocation or displacement of atoms in the crystal structure, while the effect of thermal neutrons is a nuclear transmutation that can significantly change the properties of the material. The type and intensity of damage is based on the characteristics of the material, the flow of neutrons and the modes of neutrons interaction with the atomic structures of the material, among others. This work, alluding to nuclear transmutation, makes an analysis of neutron activation of all isotopes in a steel boiling water nuclear reactor (BWR) vessel. An analytical expression is obtained in order to model activity of steel, on the basis of the weight percentage of its atomic components. Its activity is theoretically estimated in a witness sample of the same material as that of the vessel, placed within the nuclear reactor since the beginning of its commercial operation in April 1995, up to August 2010. It was theoretically determined that the witness sample, with a 0.56 g mass (1 x 1 x 0.07 cm 3 dimensions or equivalent) does not present a radiological risks during the stage of preparation, observation and analysis of it in electron microscopy and X-ray diffraction equipment s. The theoretical results were checked experimentally by measuring the activity of the sample by means of gamma spectrometry, measurement of the exposure levels around the sample, as well as the induced level to whole body and limbs, using thermo-luminescent dosimetry (TLD). As a result of the theoretical analysis, new chemical elements are predicted, as a result of the activation phenomena and radioactive decay, whose presence can be a fundamental factor of change in the properties of the vessel. This work is a preamble to the investigation of

  18. Lower detectable limit of sulfur by fast neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Shani, G; Cohen, D [Ben-Gurion Univ. of the Negev, Beersheba (Israel). Dept. of Nuclear Engineering

    1976-07-01

    For the purpose of air pollution research, the possibility of fast neutron activation analysis of sulfur was investigated. The only reaction that can be used for this purpose is S/sup 34/(n, p)P/sup 34/. A rabbit system was installed, synchronized with a 150 kV D-T neutron generator and an electronic analysing system. The whole system was operated so that the sample was irradiated for 10 sec and the 2.13 MeV ..gamma..-ray was counted for 10 sec. 5 samples were prepared containing sulfur from 0.5 to 0.1 g. Each measurement lasted 30 min and the activity was plotted as a function of sulfur weight. The relative error is increased very much when the amount of sulfur is below 0.1 g. This is what sets the lower detectable limit. Collection of more than 0.1 g of sulfur even during a long collection time means a very high SO/sub 2/ concentration in the air.

  19. Manganese determination om minerals by activation analysis, using the californium-252 as a neutron source

    International Nuclear Information System (INIS)

    Cardoso, Antonio

    1976-01-01

    Neutron Activation Analysis, using a Californium-252 neutron source, has been applied for the determination of manganese in ores such as pyrolusite, rodonite (manganese silicate)' and blending used in dry-batteries The favorable nuclear properties of manganese, such as high thermal neutron cross-section for the reaction 55 Mn (n.gamma) 56 Mn, high concentration of manganese in the matrix and short half - life of 56 Mn, are an ideal combination for non-destructive analysis of manganese in ores. Samples and standards of manganese dioxide were irradiated for about 20 minutes, followed by a 4 to 15 minutes decay and counted in a single channel pulse-height discrimination using a NaI(Tl) scintillation detector. Counting time was equal to 10 minutes. The interference of nuclear reactions 56 Fe(n,p) 56 Mn and 59 Co (n, α) 56 were studied, as well as problems in connection with neutron shadowing during irradiation, gamma-rays attenuation during counting and influence of granulometry of samples. One sample,was also analysed by wet-chemical method (sodium bismuthate) in order to compare results. As a whole, i t was shown that the analytical method of neutron activation for manganese in ores and blending, is a method simple, rapid and with good precision and accuracy. (author)

  20. Neutron activation analysis for the optimal sampling and extraction of extractable organohalogens in human hari

    International Nuclear Information System (INIS)

    Zhang, H.; Chai, Z.F.; Sun, H.B.; Xu, H.F.

    2005-01-01

    Many persistent organohalogen compounds such as DDTs and polychlorinated biphenyls have caused seriously environmental pollution problem that now involves all life. It is know that neutron activation analysis (NAA) is a very convenient method for halogen analysis and is also the only method currently available for simultaneously determining organic chlorine, bromine and iodine in one extract. Human hair is a convenient material to evaluate the burden of such compounds in human body and dan be easily collected from people over wide ranges of age, sex, residential areas, eating habits and working environments. To effectively extract organohalogen compounds from human hair, in present work the optimal Soxhelt-extraction time of extractable organohalogen (EOX) and extractable persistent organohalogen (EPOX) from hair of different lengths were studied by NAA. The results indicated that the optimal Soxhelt-extraction time of EOX and EPOX from human hair was 8-11 h, and the highest EOX and EPOX contents were observed in hair powder extract. The concentrations of both EOX and EPOX in different hair sections were in the order of hair powder ≥ 2 mm > 5 mm, which stated that hair samples milled into hair powder or cut into very short sections were not only for homogeneous. hair sample but for the best hair extraction efficiency.

  1. Neutron activation analysis

    International Nuclear Information System (INIS)

    Taure, I.; Riekstina, D.; Veveris, O.

    2004-01-01

    Neutron activation analysis (NAA) in Latvia began to develop after 1961 when nuclear reactor in Salaspils started to work. It provided a powerful neuron source, which is necessary for this analytical method. In 1963 at Institute of Physics of the Latvian Academy of Sciences the Laboratory of Neutron Activation Analysis was formed. At the first stage of development the main tasks were of theoretical and technical aspects of NAA. Later the NAA was used to solve problems in technology, biology, and medicine. In the beginning of the 80-ties more attention was focussed to the use of NAA in the environmental research. Environmental problems stayed the main task till the closing the nuclear reactor in Salaspils in 1998 that ceased the main the existence of the laboratory and of NAA, this significant and powerful analytical method in Latvia and Baltic in general. (authors)

  2. Determination of inorganic component in plastics by neutron activation analysis

    International Nuclear Information System (INIS)

    Mateus, Sandra Fonseca; Saiki, Mitiko

    1995-01-01

    In order to identify possible sources of heavy metals in municipal solid waste incinerator ashes, plastic materials originated mainly from household waste were analyzed by using instrumental neutron activation analysis method. Plastic samples and synthetic standards of elements were irradiated at the IEA-R1 nuclear reactor for 8 h under thermal neutron flux of about 10 13 n cm -2 s -1 . After adequate decay time, counting were carried out using a hyperpure Ge detector and the concentrations of the elements As, Ba, Br, Cd, Co, Cr, Fe, Sb, Sc, Se, Sn, Ti and Zn were determined. For some samples, not all these elements were detected. Besides, the range of concentrations determined in similar type and colored samples varied from a few ppb to percentage. In general, colored and opaque plastic samples presented higher concentrations of the elements than those obtained from transparent and milky plastics. Precision of the results was also evaluated. (author). 3 refs., 2 tabs

  3. Neutron activation determination of impurities in molybdenite and galena

    International Nuclear Information System (INIS)

    Blinov, V.A.; Gavrilov, V.M.; Zherekhov, V.G.; Egorov, Yu.E.; Krivokhatskij, A.S.

    1975-01-01

    A method is described for non-destructive neutron-activation determination of 14 chemical elements (Na, Ag, Zn, Sc, La, Eu, Tb, Yb, Sb, Ta, Gr, Se, Fe and Co) in molybdenite and galenite minerals. The samples and standards of Ag, Se, Co and Np have been wrapped in an aluminium foil and packed in an aluminium container; they have been then irradiated for 10 hr in the vertical channel of a nuclear reactor with flux of thermal neutrons (3.0, 0.45)x10 13 n/cm 2 xsec to record the γ-spectra of the samples and standards 1, 5, 16, 65, 265 and 350 days after irradiation on a γ-spectrometer with a Ge(Li)-detector. The results are found to be in a good agreement with the spectra of Ag, Sb, La and Fe

  4. Neutron activation analysis

    International Nuclear Information System (INIS)

    Okada, Yukiko

    2005-01-01

    Trends and progress in neutron activation analysis (NAA) for the period starting in 1999 to 2003 are presented. Numbers of published reports on NAA are decreasing year by year as investigated from the database JST and NUCLEN. Summary reports on the international conferences held on NAA are followed by classifying according to the fields: various measurement techniques and application fields. Specially focused topics are newly developed techniques for measuring trace elements with high sensitivity and high accuracy such as (1) by diminishing the Compton-background gamma-rays using anti-coincidence technique, (2) by using prompt-gamma rays measurement method (PGAA) and (3) by using a gamma-ray detector array (GEMINI), which has succeeded in a simultaneous quantification of 27 elements from a standard rock sample having a weight of only 10 milligrams, and others. These techniques will be applied in the space and earth sciences and medical fields. (S. Ohno)

  5. Methodology for iodine-129 determination in coniferous plant by neutron activation

    International Nuclear Information System (INIS)

    Quintana, E.E.; Thyssen, S.M.

    1998-01-01

    Full text: The measurement methods of iodine-129 ( 129 I) include liquid scintillation counting, mass spectrometry analysis, X-ray spectrometry and neutron activation analysis. The combination of long half-life and low radiation energy, limit the sensitivity of a direct measurement in environmental matrixes. The neutron activation analysis (NAA) permits the increase in the sensitivity because of the high thermal neutron cross section of 129 I. The reaction produced is 129 I (n,γ) 130 I and the Eγ (536 keV) of iodine-130 (t 1/2 = 12,6 hours) is measured. The developed methodology allows the determination of 129 I in coniferous needles using NAA. The chemical treatment removes the interferences present in the matrix, as well as the Bromine-82 originated in the activation process. The analytical method is divided in six steps: a) digestion by alkaline fusion; b) radiochemical purification of 129 I by distillation followed by solvent extraction; c) distillation and adsorption on activated charcoal; d) neutron irradiation; e) radiochemical purification of 130 I by distillation followed by solvent extraction; f) gamma spectrometry. Iodine-131 tracer is added, and a chemical recovery of 95% in the distillations is obtained. The whole process recovery is within 70% and 85%. The detection limit is 0.48 mBq. Several factors affect this value, such as sample type, variety of coniferous, natural iodine concentration, irradiation time and neutron flux. (author) [es

  6. Determining the amount of Br, Na and K in six wheat samples with neutron activation analysis (NAA) method in Arak, I.R. Iran

    International Nuclear Information System (INIS)

    Reza Pourimani; Khatoon Abasnejad; Khadijeh Ghanbarzadeh; Mohammad Reza Zare; Mahdi Kamali

    2013-01-01

    Accurate knowledge of the trace elemental concentrations in wheat and its products is of great importance from a nutritional point of view. In this study, six wheat samples were prepared from the agriculture research center of Arak named Sardari, Amir, MV-17, Batava, Karaj-2 and Alvand; they were analyzed by neutron activation method (NAA). In this method, Isfahan miniature reactor as a neutron source and relative NAA method has been used as the analysis type. In this design in order to record gamma spectrum the MCA system and high purity germanium detector were used. Finally, the concentration of the trace elements such as Br, K and Na value was determined for the Sardari, Amir, Alvand, MV-17, Batava, Karaj-2 wheat samples. The average concentration of trace elements in all wheat samples in the studied area are 2.41(0.8597-6.1175) mg kg -1 for Br, 13.42(8.7063-24.696) mg kg -1 for Na and 463.30(434.22-505.45) mg kg -1 for K, respectively. These were compared with other reports results. This study has been conducted as the first time for this region. (author)

  7. Applications of short-lived activation products in neutron activation analysis of bio-environmental specimens

    International Nuclear Information System (INIS)

    1987-03-01

    This report discusses the advantages and disadvantages, special techniques, and actual and potential applications of neutron activation analysis (NAA) utilizing short-lived neutron-induced products, with special reference to the analysis of samples of biological and environmental origin. Attention is devoted mainly to products having half-lives in roughly the range of 10 milliseconds to 60 seconds, but with some discussion of the usefulness of even shorter-lived species, and ones with half-lives as long as a few minutes. Important aspects of the analytical methodology include sample preparation, irradiation/transfer systems, activity measurements, data processing and analytical quality assurance. It is concluded that several trace elements can be determined in bio-environmental samples (as well as in samples of industrial, geochemical and other origin). In particular, this method provides analytical possibilities for several elements (e.g. B, F, Li and V) that are difficult to determine in some matrices at trace levels by any other technique. These conclusions are illustrated in an annex by results of calculations in which the applicability of the techniques to the analysis of several biological and environmental reference materials is evaluated by means of an advance computer prediction program. The report concludes with an annotated bibliography of relevant publications (including abstracts, where available) taken from the INIS database. (author)

  8. Determination of rhenium in molybdenite by neutron-activation analysis.

    Science.gov (United States)

    Terada, K; Yoshimura, Y; Osaki, S; Kiba, T

    1967-01-01

    A neutron-activation method is described for the determination of rhenium in molybdenite. Radiochemical separation by a carrier technique was carried out very rapidly by means of successive liquid-liquid extraction processes. The recovery of rhenium, which was determined by a spectrophotometric method, was about 93%. About 10 samples could be analysed within 6 hr in parallel runs.

  9. The instrumental neutron-activation analysis of granites from the Bushveld Complex

    International Nuclear Information System (INIS)

    Watterson, J.I.W.

    1978-01-01

    Three methods of instrumental neutron-activation analysis, 14MeV, reactor thermal, and reactor epithermal, are compared for the analysis of granites form the Bushveld Complex. A total of 34 elements can be determined in the granites by these methods. Samples from the Zaaiplaats area were analysed by thermal neutron activation, and 22 elements were determined in all of them. These elements were used to distinguish between the mineralized Bobbejaankop and Lease granites and the Main granite by the use of multivariate statistics. The Bobbejaankop granite appears as a more-differentaited rock carrying greater amounts of the incompatible elements than does the Main granite [af

  10. Performance of an active well coincidence counter for HEU samples

    International Nuclear Information System (INIS)

    Ferrari, Francesca; Peerani, Paolo

    2010-01-01

    Neutron coincidence counting is the reference NDA technique used in nuclear safeguards to measure the mass of nuclear material in samples. For high-enriched uranium (HEU) samples active neutron interrogation is generally performed and the most common device used by nuclear inspectors is the Active Well Coincidence Counter (AWCC). Within her master thesis at the Polytechnic of Milan, the first author performed an intensive study on the characteristics and performances of the AWCC in order to assess the 235 U mass in HEU oxide samples at the PERLA laboratory of JRC. The work has been summarised in this paper that starts with the optimisation of the use of AWCC for nuclear safeguards, describing the calibration procedure, reporting results of a series of verification measurements, summarising the performances that can be obtained with this instruments during inspections at fuel production plants and concluding with the discussion of uncertainties related to these measurements.

  11. Study of the trace element in organisms by neutron activation analysis, 1. Multielement instrumental neutron activation analysis of cannabis

    Energy Technology Data Exchange (ETDEWEB)

    Shinogi, M; Murai, Y; Mori, I [Kobe Women' s Coll. of Pharmacy (Japan); Takeuchi, T

    1974-12-01

    Examinations were made on optimal experimental conditions for instrumental determination of various elements in cannabis by neutron activation analysis, without any radiochemical separation, and the following conditions were found to be useful. Irradiation samples to be used are about 300 mg of the leaves or stem bark, and about 100 mg of the root. For soil sample, about 50 mg is used for the determination of short half-life nuclides and about 300 mg for long half-life nuclides. For short half-life nuclides, the samples are irradiated for 1 min, activity is measured for 200 sec after a decay of 3 min, and for 400 sec after a decay of 10 min. For long half-life nuclides, the samples are irradiated for 60 min and the activites are measured for 4 K sec after 1 week and for 10 K sec after 1 month. Use of supersonic waves is also convenient for cleansing of the samples. Thirty-five kinds of interesting elements were determined by this method from cannabis cultivated in Maizuru area.

  12. 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

  13. Instrumental neutron activation analysis of environmental samples from a region with prevalence of population disabilities in the North Gondar, Ethiopia

    International Nuclear Information System (INIS)

    Bitewlign, T.A.; Addis Ababa University, Addis Ababa; Chaubey, A.K.; Beyene, G.A.; Melikegnaw, T.H.; Mizera, Jiri; Czech Academy of Sciences, Prague; Kamenik, Jan; Krausova, Ivana; Kucera, Jan

    2017-01-01

    Instrumental neutron activation analysis (INAA) of soil, coal, water, and crops from the village of Awdarda in the North Gondar, Ethiopia, where the residents suffer from various disabilities, was performed in an attempt to elucidate the existing health problems. More than forty elements were determined in the samples analyzed. Comparison of our results with literature values indicates highly elevated contents of terrigenous elements in Awdarda cereals, possibly due to contamination by excavation and indoor combustion of local coal-bearing sediments. Impact is discussed of the elevated aluminium and the rare earth elements levels in crops on the health problems. (author)

  14. Standard Test Method for Oxygen Content Using a 14-MeV Neutron Activation and Direct-Counting Technique

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2007-01-01

    1.1 This test method covers the measurement of oxygen concentration in almost any matrix by using a 14-MeV neutron activation and direct-counting technique. Essentially, the same system may be used to determine oxygen concentrations ranging from over 50 % to about 10 g/g, or less, depending on the sample size and available 14-MeV neutron fluence rates. Note 1 - The range of analysis may be extended by using higher neutron fluence rates, larger samples, and higher counting efficiency detectors. 1.2 This test method may be used on either solid or liquid samples, provided that they can be made to conform in size, shape, and macroscopic density during irradiation and counting to a standard sample of known oxygen content. Several variants of this method have been described in the technical literature. A monograph is available which provides a comprehensive description of the principles of activation analysis using a neutron generator (1). 1.3 The values stated in either SI or inch-pound units are to be regarded...

  15. Selenium contents of Japanese foodstuffs by neutron activation analysis

    International Nuclear Information System (INIS)

    Noda, Katsuhiko; Hirai, Shoji; Danbara, Hiroshi.

    1980-01-01

    Selenium (Se) contents of Japanese foodstuffs were measured by neutron activation analyses with the TRIGA-II reactor in Atomic Energy Research Laboratory, Musashi Institute of Technology. Freezedried samples (200 - 500 mg) were irradiated in the pneumatic tube (thermal neutron flux, 1 x 10 12 n.cm -2 . sec -1 ) for 10 sec, and sup(77m)Se produced was counted for 30 sec in a gamma -ray spectrometer system equipped with a Ge(Li) detector. Samples containing less than 0.05 ppm Se and the processed foods of high salt contents were analyzed with radioactivities of 75 Se after irradiation in the central symble (thermal neutron flux, 4 x 10 12 n.cm -2 .sec -1 ) for 5 hours, digestion in the HNO 3 -HClO 4 mixture, and then purification by a precipitation process. Foodstuffs of animal origins contained more Se than those of plant origins. Se contents were as follows in the descending order: fish, meats, cereals, vegetables, and fruit. Daily per capital intaked of Se was in the range of 100 - 200 mu g, as calculated for and as found by analysis of composite diets representing ordinary Japanese meals. (author)

  16. Detection of hidden explosives by fast neutron activation analysis

    International Nuclear Information System (INIS)

    Li Xinnian; Guo Junpeng; Luo Wenyun; Wang Chuanshan; Fang Xiaoming; Yu Tailiu

    2008-01-01

    The paper describes the method and principle for detection of hidden explosive by fast neutron activation analysis (FNAA). The method of detection of explosives by FNAA has the specific properties of simple determination equipments, high reliability, and low detecting cost, and would be beneficial to the applicability and popularization in the field of protecting and securing nation. The contents of nitrogen and oxygen in four explosives, more then ten common materials and TNT samples covered with soil, were measured by FNAA. 14 MeV fast neutrons were generated from (d, t) reaction with a 400 kV Cockcroft Walton type accelerator. The two-dimension distributions for nitro- gen and oxygen counting rates per unit mass of determined matters were obtained, and the characteristic area of explosives and non-explosives can be defined. By computer aided pattern recognition, the samples were identified with low false alarm or omission rates. The Monte-Carlo simulation indicates that there is no any radiation at 15 m apart from neutron source and is safe for irradiation after 1 h. It is suggested that FNAA may be potential in remote controlling for detection hidden explosive system with multi-probe large array. (authors)

  17. Trace element analysis of common salt using neutron activation analysis

    International Nuclear Information System (INIS)

    Usman, K.

    1993-01-01

    Instrumental Fast Neutron Activation Analysis (IFNAA) technique has been used in the qualitative and quantitative determination of the impurity elements in common salt. Samples of the different types of common salt processed in Nigeria and some of those imported into the country were used. The type A711 KAMAN neutron generator and a high-purity Germanium (HpGe) gamma spectrometer available at the Centre for Energy Research and Training, Ahmadu Bello University, Zaria has been used. The ORTEC ADCAM 100 Emulation Software (Maestro) was used in the qualitative measurement of the detected elements. The G.R.G Activation Analysis System by G. R. Gilmore, 1987, was used in the quantitative determination of the elements detected by relative method. Aluminium and arsenic were detected and measured

  18. Estimation of iodine in soils by neutron activation analysis

    International Nuclear Information System (INIS)

    Krishnamoorthy, K.R.; Iyer, R.K.

    1982-01-01

    This paper reports the determination of the iodine content of soils by neutron activation analysis. The irradiated sample is fused with alkali in presence of 131 I tracer. From the aqueous extract, iodine activity is extracted into carbon tetrachloride and stripped back to aqueous phase with a high selectivity for iodine. 131 I tracer is used to measure chemical yield. Iodine contents in the range 1 to 20 ppm. have been determined by this technique. (author)

  19. Neutron activation analysis (NAA), radioisotope production via neutron activation (PNA) and fission product gas-jet (GJA)

    Energy Technology Data Exchange (ETDEWEB)

    Gaeggeler, H W [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1996-11-01

    Three different non-diffractive applications of neutrons are outlined, neutron activation analysis, production of radionuclides, mostly for medical applications, and production of short-lived fission nuclides with a so-called gas-jet. It is shown that all three devices may be incorporated into one single insert at SINQ due to their different requests with respect to thermal neutron flux. Some applications of these three facilities are summarized. (author) 3 figs., 1 tab., 8 refs.

  20. Neutron activation analysis (NAA), radioisotope production via neutron activation (PNA) and fission product gas-jet (GJA)

    International Nuclear Information System (INIS)

    Gaeggeler, H.W.

    1996-01-01

    Three different non-diffractive applications of neutrons are outlined, neutron activation analysis, production of radionuclides, mostly for medical applications, and production of short-lived fission nuclides with a so-called gas-jet. It is shown that all three devices may be incorporated into one single insert at SINQ due to their different requests with respect to thermal neutron flux. Some applications of these three facilities are summarized. (author) 3 figs., 1 tab., 8 refs

  1. The investigation of fast neutron Threshold Activation Detectors (TAD)

    International Nuclear Information System (INIS)

    Gozani, T; King, M J; Stevenson, J

    2012-01-01

    The detection of fast neutrons is usually done by liquid hydrogenous organic scintillators, where the separation between the ever present gamma rays and neutrons is achieved by the pulse shape discrimination (PSD). In many practical situation the detection of fast neutrons has to be carried out while the intense source (be it neutrons, gamma rays or x-rays) that creates these neutrons, for example by the fission process, is present. This source, or ''flash'', usually blinds the neutron detectors and temporarily incapacitates them. By the time the detectors recover the prompt neutron signature does not exist. Thus to overcome the blinding background, one needs to search for processes whereby the desired signature, such as fission neutrons could in some way be measured long after the fission occurred and when the neutron detector is fully recovered from the overload. A new approach was proposed and demonstrated a good sensitivity for the detection of fast neutrons in adverse overload situations where normally it could not be done. A temporal separation of the fission event from the prompt neutrons detection is achieved via the activation process. The main idea, called Threshold Activation Detection (or detector)-TAD, is to find appropriate substances that can be selectively activated by the fission neutrons and not by the source radiation, and then measure the radioactively decaying activation products (typically beta and γ-rays) well after the source pulse has ended. The activation material should possess certain properties: a suitable half-life; an energy threshold below which the numerous source neutrons will not activate it (e.g. about 3 MeV); easily detectable activation products and has a usable cross section for the selected reaction. Ideally the substance would be part of the scintillator. There are several good candidates for TAD. The first one we have selected is based on fluorine. One of the major advantages of this element is the fact that it is a major

  2. The investigation of fast neutron Threshold Activation Detectors (TAD)

    Science.gov (United States)

    Gozani, T.; King, M. J.; Stevenson, J.

    2012-02-01

    The detection of fast neutrons is usually done by liquid hydrogenous organic scintillators, where the separation between the ever present gamma rays and neutrons is achieved by the pulse shape discrimination (PSD). In many practical situation the detection of fast neutrons has to be carried out while the intense source (be it neutrons, gamma rays or x-rays) that creates these neutrons, for example by the fission process, is present. This source, or ``flash'', usually blinds the neutron detectors and temporarily incapacitates them. By the time the detectors recover the prompt neutron signature does not exist. Thus to overcome the blinding background, one needs to search for processes whereby the desired signature, such as fission neutrons could in some way be measured long after the fission occurred and when the neutron detector is fully recovered from the overload. A new approach was proposed and demonstrated a good sensitivity for the detection of fast neutrons in adverse overload situations where normally it could not be done. A temporal separation of the fission event from the prompt neutrons detection is achieved via the activation process. The main idea, called Threshold Activation Detection (or detector)-TAD, is to find appropriate substances that can be selectively activated by the fission neutrons and not by the source radiation, and then measure the radioactively decaying activation products (typically beta and γ-rays) well after the source pulse has ended. The activation material should possess certain properties: a suitable half-life; an energy threshold below which the numerous source neutrons will not activate it (e.g. about 3 MeV); easily detectable activation products and has a usable cross section for the selected reaction. Ideally the substance would be part of the scintillator. There are several good candidates for TAD. The first one we have selected is based on fluorine. One of the major advantages of this element is the fact that it is a major

  3. Analysis of marine samples by neutron-induced prompt gamma-ray technique and ICP-MS

    International Nuclear Information System (INIS)

    Yonezawa, C.; Matsue, H.; McKay, K.; Povinec, P.

    2001-01-01

    Multi-element and isotopic analyses of oils and marine environmental samples were carried out to estimate a contamination source using a 'finger printing' method. Elemental analyses were carried out using neutron-induced prompt gamma-ray analysis (PGA), instrumental neutron activation analysis (INAA) at the Japan Atomic Institute, Tokai-mura, Japan (JAERI) and ICP-MS in the IAEA Marine Environment Laboratory, Monaco (MEL). Fifteen elements including light elements, H, B, N, Si and Ca, which cannot be determined by INAA and ICP-MS, were determined by PGA. A total of 47 elements were determined in the present study. The potential of PGA for the determination of isotopic ratios was tested by measuring 34 S/ 32 S ratios in oils. The evaluation of historical records of marine environmental conditions using annual bands in coral samples was also investigated. (author)

  4. Determination of mercury in food by neutron activation

    International Nuclear Information System (INIS)

    Anand, S.J.S.

    1976-01-01

    Determination of mercury in food samples has been carried out by neutron activation followed by chemical separation to remove the interfering activities of copper, zinc etc. Chemical separation was carried out using anion exchange resin (DOWEX 1x8). Mercury was determined by counting 77 keV γ-rays of 197 Hg on a NaI(Tl) crystal in conjunction with a 400-channel pulse-height analyser. Levels of mercury in the following foods are tabulated: rice, wheat, pulses, millets, leafy vegetables, flower, carrot, potato, tomato, onion, chilli powder, sugar, tea leaves, milk. (T.I.)

  5. Determination of mercury in food by neutron activation

    Energy Technology Data Exchange (ETDEWEB)

    Anand, S J.S. [Bhabha Atomic Research Centre, Bombay (India). Air Monitoring Section

    1976-01-01

    Determination of mercury in food samples has been carried out by neutron activation followed by chemical separation to remove the interfering activities of copper, zinc etc. Chemical separation was carried out using anion exchange resin (DOWEX 1x8). Mercury was determined by counting 77 keV ..gamma..-rays of /sup 197/Hg on a NaI(Tl) crystal in conjunction with a 400-channel pulse-height analyser. Levels of mercury in the following foods are tabulated: rice, wheat, pulses, millets, leafy vegetables, flower, carrot, potato, tomato, onion, chilli powder, sugar, tea leaves, milk.

  6. Mercury determination in dentist's hair and nails by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Mazzilli, B.; Munita, C.S.

    1986-01-01

    The mercury in scalp hair and fingernails of a group of dentists who usually handle with this toxic element in their profession is determined. The results were obtained by instrumental neutron activation analysis. The experimental procedure was based on the evaluation of the 197 Hg photopeak area, whose half life is 65h. After at a neutron fluxo of 5x10 12 n.cm -2 .sec -1 , the activity of the samples were measured by using a solid state Ge (Li) detector coupled to a 4.096 channel pulse height analyser. (M.A.C.) [pt

  7. Major and trace elements assessment in sediment samples from Rio Grande Reservoir, by neutron activation analysis

    International Nuclear Information System (INIS)

    Franklin, Robson L.; Ferreira, Francisco J.; Favaro, Deborah I.T.; Bevilacqua, Jose Eduardo

    2009-01-01

    The Rio Grande Reservoir, Southeast of the Sao Paulo Metropolitan Area (SPMA) supplies water for four counties (Sao Bernardo do Campo, Sao Caetano do Sul, Santo Andre and Diadema). It has been seriously affected by urban expansion, due to chaotic urban occupation and improper use of the surrounding areas. In this study bottom sediment samples were collected, by using a Van Veen sampler, during the dry and rainy seasons. Four sampling points were defined by using GPS and are located at the mouth of the Rio Grande and Ribeirao Pires Rivers, in the middle of the reservoir and near the catchment point of the water supply. The sediment samples were submitted to instrumental neutron activation analysis (INAA) and the following elements were determined: As, Ba, Br, Co, Cr, Cs, Rb, Sb, Sc, Se, Ta, Th, U e Zn and the rare earth elements Ce, Eu, La, Lu, Nd, Sm, Tb, Yb. Short irradiation was also performed for total Hg determination by NAA using 197 Hg radioisotope. This was possible due to the high Hg concentration levels in these sediments. The methodology validation was carried out by certified reference material analyses. The results obtained for multielemental concentrations in the sediment samples were compared to NASC (North American Shale Composite) values. The concentration values obtained for As and metals Cr, Hg and Zn in the sediment samples were compared to the Canadian Council of Minister of the Environment (CCME) oriented values (TEL and PEL values) and adopted by CETESB. (author)

  8. Determination of the provenance of obsidian samples collected in the archaeological site of San Miguel Ixtapan, Mexico State, Mexico by means of neutron activation analysis

    International Nuclear Information System (INIS)

    Almazan-Torres, M.G.; Aguirre-Martinez, P.I.

    2004-01-01

    Obsidian samples from San Miguel Ixtapan Mexico State, Mexico were analyzed by means of neutron activation. Statistical treatments such as bivariate, cluster and principal-components analyses were applied to the data set. Obsidians were identified as coming from three important sources: Sierra of Pachuca in the state of Hidalgo, Zinap uaro and Zin aro-Varal in the state of Michoacan. (author)

  9. A theoretical model for predicting neutron fluxes for cyclic Neutron ...

    African Journals Online (AJOL)

    A theoretical model has been developed for prediction of thermal neutron fluxes required for cyclic irradiations of a sample to obtain the same activity previously used for the detection of any radionuclide of interest. The model is suitable for radiotracer production or for long-lived neutron activation products where the ...

  10. Measurement of the loss on ignition of bulk calcined bauxite samples by neutron moderation

    International Nuclear Information System (INIS)

    Aylmer, J.A.; Borsaru, M.

    1985-01-01

    The production of high-grade calcined bauxite is very dependent on the moisture content of the final product. Existing procedures rely on the ignition of small samples to monitor the effectiveness of the calcination process. The results obtained by this gravimetric technique are several hours behind production and do not permit regular adjustment of the furnace to optimize the control of the chemically bound water content (LOI). To provide rapid and more relevant results, a neutron moderation technique has been developed for measuring the LOI of bulk samples of calcined bauxite while they are still hot. The method uses fast neutrons from an 241 Am-Be neutron source to irradiate the samples, and the backscattered thermal neutrons detected are a measure of bound moisture content. The rms deviation between neutron and conventional determinations of LOI, in 15 calcined bauxite samples, was 0.08 per cent LOI over the range 0.1 to 0.9 per cent LOI. When allowance is made for the rms error in the ignition method, the error in the neutron method is found to be 0.07 per cent LOI

  11. Activation of 45-MeV proton irradiation and proton-induced neutron irradiation in polymers

    International Nuclear Information System (INIS)

    Ra, Se-Jin; Kim, Kye-Ryung; Jung, Myung-Hwan; Yang, Tae-Keon

    2010-01-01

    During beam irradiation experiments with more than a few MeV energetic protons, the sample activation problem can be very severe because it causes many kinds of additional problems for the post-processing of the samples, such as time loss, inconvenience of sample handling, personal radiation safety, etc. The most serious problem is that immediate treatment of the sample is impossible in some experiments, such as nano-particle synthesizing. To solve these problems, we studied why the samples are activated and how the level of the activation can be reduced. It is known that the main reasons of activation are nuclear reactions with elements of the target material by primary protons and secondary produced neutrons. Even though the irradiation conditions are same, the level of the activation can be different depending on the target materials. For the nanoparticle synthesizing experiments, the target materials can be defined as the container and the sample itself. The reduction of the activation from the container is easier than the reduction from the sample. Therefore, we tried to reduce the activation level by changing the container materials. In this paper, the results are displayed for some candidate container materials, such as polymethyl methacrylate, polystyrene, Glass, etc., with 45-MeV and 10-nA proton beams. As a result, PS is the most suitable material for the container because of its relatively low level of the activation by protons. Also the contribution of secondary produced neutrons to the activation is negligible.

  12. Nondestructive neutron activation analysis of silicon carbide

    Energy Technology Data Exchange (ETDEWEB)

    Vandergraaf, T. T.; Wikjord, A. G.

    1973-10-15

    Instrumentel neutron activation analysis was used to determine trace constituents in silicon carbide. Four commercial powders of different origin, an NBS reference material, and a single crystal were characterized. A total of 36 activation species were identified nondestructively by high resolution gamma spectrometry; quantitative results are given for 12 of the more predominant elements. The limitations of the method for certain elements are discussed. Consideration is given to the depression of the neutron flux by impurities with large neutron absorption cross sections. Radiation fields from the various specimens were estimated assuming all radionuclides have reached their saturation activities. (auth)

  13. Multielement analysis of rice flour-unpolished reference material by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Suzuki, Shogo; Hirai, Shoji

    1990-01-01

    Trace elements in NIES certified reference material No. 10-a∼10-c Rice Flour-Unpolished, prepared by the National Institute for Environmental Studies of Japan (NIES), were determined by instrumental neutron activation analysis (INAA). A set of three samples with different Cd concentration levels was subjected to analyses. Portions of each sample (ca. 200∼1000 mg) were irradiated, either with thermal neutrons without cadmium filter or with epithermal neutrons with cadmium filter, in the Musashi Institute of Technology Research Reactor (MITRR). The activated samples were analyzed by the three methods; conventional γ-ray spectrometry using a coaxial Ge detector, anticoincidence counting spectrometry, and coincidence counting spectrometry using a coaxial Ge detector and a well type NaI(Tl) detector. Concentrations of 26∼28 elements were determined by these methods. The values obtained for many elements, except for Mg and K, were in good agreement with those of the NIES certified and reference. Concentrations of 10 elements (S, Sc, V, Ag, Sb, Cs, Ba, La, Sm, Th), whose certified or reference values are not available from NIES, were also determined in this work. (author)

  14. Determination of Mercury in Aqueous Samples by Means of Neutron Activation Analysis with an Account of Flux Disturbances

    Energy Technology Data Exchange (ETDEWEB)

    Brune, D; Jirlow, K

    1967-08-15

    The technique of low temperature neutron irradiation combined with isotopic exchange separation technique has been applied in the determination of mercury in aqueous samples. The kinetics of the isotopic exchange reaction has been studied for various sample volumes. The effect of the flux perturbation caused by aqueous samples has been investigated for samples of various size and geometry in a central position in a well moderated heavy water reactor. The effect has been studied both theoretically and experimentally. The 'Thermos' code has been used in the calculations.

  15. Determination of Mercury in Aqueous Samples by Means of Neutron Activation Analysis with an Account of Flux Disturbances

    International Nuclear Information System (INIS)

    Brune, D.; Jirlow, K.

    1967-08-01

    The technique of low temperature neutron irradiation combined with isotopic exchange separation technique has been applied in the determination of mercury in aqueous samples. The kinetics of the isotopic exchange reaction has been studied for various sample volumes. The effect of the flux perturbation caused by aqueous samples has been investigated for samples of various size and geometry in a central position in a well moderated heavy water reactor. The effect has been studied both theoretically and experimentally. The 'Thermos' code has been used in the calculations

  16. Provenience studies of the Ko-Kutani ware by neutron activation analysis

    International Nuclear Information System (INIS)

    Kawashima, Tatsuro.

    1990-01-01

    The instrumental neutron activation analysis has been applied to the multielemental analysis of eight samples of the Ko-Kutani ware including the Aote's that is one of semi-porcelain body. Each sample was compared with concentration of the useful index element, such as Ta, Sc, Ba, Hf, Th and rare earth, to discriminate the Arita group from the Kutani group. Eight samples were judged as products of the Arita, just as in previous paper. (author)

  17. Activation measurements for fast neutrons. Part A. Sulfur (32P) activation

    International Nuclear Information System (INIS)

    Kerr, George D.

    2005-01-01

    The sulfur activation measurements at Hiroshima have been useful in refining and verifying the neutron source-term calculations for the Hiroshima bomb (Kerr and Pace 1988). For example, the Riken measurements of sulfur activation at Hiroshima were used to demonstrate that a two dimensional calculation of the neutron leakage was required for the Hiroshima bomb in order to accurately account for the blind spot in the neutron leakage through the nose of the device (Kerr 1982a,b; Kerr et al. 1983; Pace and Kerr 1984). The sulfur activation measurements at Hiroshima are discussed and compared in this section with the results of DS86 and DS02 calculations for the air-over-ground transport of neutrons at Hiroshima. (J.P.N.)

  18. Protein determination in soya bean by fast neutron activation analysis

    International Nuclear Information System (INIS)

    Szegedi, S.; Mosbah, D.S.; Varadi, M.; Szaloki, I.

    1988-01-01

    For a non-destructive determination of the protein content in soya bean samples, 14-MeV neutron activation analysis was applied. To check the method, the results obtained by X-ray fluorescence analysis and the Kjeldahl procedure were compared. For pressed pellet samples of about 1 g with 15 min irradiation and 10 min measuring times the accuracy of the protein determination was found to be 15%. (author) 7 refs.; 4 figs.; 3 tabs

  19. Elemental analysis of bottom ash from municipal incinerator by neutron activation analysis

    International Nuclear Information System (INIS)

    Kim, S. H.; Jang, S. H.; Moon, J. H.; Jung, Y. S.; Kim, Y. J.

    2003-01-01

    Elemental analysis of bottom ash generated from municipal solid waste incinerator was performed by neutron activation analysis. For this study, ash samples monthly collected from incinerator in D city were sieved with 5 mm mesh size, dried, pulverized by agate mortar and finally re-sieved with 200μ mesh size. Prepared samples were irradiated by neutrons using NAA No.1 irradiation hole in Korea Atomic Energy Research Institute. Activated samples were measured by gamma-ray spectrometer according to the relevant nuclear properties of target nuclides and the concentration of 33 elements were determined from the collected ash samples. Quality control was conducted by comparative analysis with two NIST standard reference materials simultaneously. Mean values and standard deviations of hazardous elements such as As, Cr, Cu, Fe, Mn, Sb and Zn among the determined elements were 3.8±6.9mg/kg, 620±0.12 %, 4.76±0.37 %, 0.26±0.10 %, 115±29 mg/kg and 0.71±0.19 %, respectively

  20. Studies on application of neutron activation analysis -Applied research on air pollution monitoring and development of analytical method of environmental samples

    International Nuclear Information System (INIS)

    Chung, Yong Sam; Moon, Jong Hwa; Chung, Young Ju; Jeong, Eui Sik; Lee, Sang Mi; Kang, Sang Hun; Cho, Seung Yeon; Kwon, Young Sik; Chung, Sang Wuk; Lee, Kyu Sung; Chun, Ki Hong; Kim, Nak Bae; Lee, Kil Yong; Yoon, Yoon Yeol; Chun, Sang Ki.

    1997-09-01

    This research report is written for results of applied research on air pollution monitoring using instrumental neutron activation analysis. For identification and standardization of analytical method, 24 environmental samples are analyzed quantitatively, and accuracy and precision of this method are measured. Using airborne particulate matter and biomonitor chosen as environmental indicators, trace elemental concentrations of sample collected at urban and rural site monthly are determined ant then the calculation of statistics and the factor analysis are carried out for investigation of emission source. Facilities for NAA are installed in a new HANARO reactor, functional test is performed for routine operation. In addition, unified software code for NAA is developed to improve accuracy, precision and abilities of analytical processes. (author). 103 refs., 61 tabs., 19 figs

  1. 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

  2. Application of neutron activation analysis for the determination of essential elements in egg samples; Aplicacao da analise por ativacao com neutrons para a determinacao de elementos essenciais em amostras de ovos

    Energy Technology Data Exchange (ETDEWEB)

    Gomes, Bruna G.; Maihara, Vera A.; Avegliano, Roseane P., E-mail: brunagabrielegomes@gmail.com, E-mail: vmaihara@ipen.br, E-mail: pagliaro@usp.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    The eggs are among the twenty foods consumed by the population of the five major regions of Brazil. Among the types of eggs, there are differences in nutritional value, which can vary according to the food of the bird. This study evaluating the elements Cl, K, Mg, Mn and Na considered essential micronutrients in food, because they are fundamental in several metabolic processes necessary for the maintenance and training of the human body. We analyzed three types of eggs: egg whites, of the quail, and the colonial in cooked and raw form, using the Instrumental Neutron Activation Analysis method (INAA). The egg samples were lyophilized and pulverized before analysis. To validate the methodology, reference materials NIST RM 8415 Whole Egg Powder and NIST SRM 1567 Wheat Flour were analyzed. The samples, reference materials and standards of the elements were irradiated for 20 seconds under a thermal neutron flux of 6,6x10{sup 12} cm -2 s -1 in the nuclear research reactor IEA-R1 of IPEN-CNEN / SP. The results were consistent with the values of the Brazilian Table of Food Composition (TACO)

  3. Determination of x mercury trace amounts in selected foodstuffs by neutron activation analysis

    International Nuclear Information System (INIS)

    Jiranek, V.; Bludovsky, R.

    1976-01-01

    Neutron activation analysis was used for the analysis of dehydrated milk, flour, coffee, tea and rice. The results were compared with those obtained by the photometric determination of mercury by dithizone. Four types of sample distribution by wet ashing were evaluated with regard to mercury volatilization in sample destruction. The samples were irradiated with thermal neutrons, a carrier was added and the samples were dissolved in the mixture of H 2 SO 4 +HClO 4 +HNO 3 . After dilution mercury was extracted using a substoichiometric amount of dithizone dissolved in chloroform. In the extract the radioactivity of 197 Hg was measured by NaI(Tl). At the average 15% accuracy of determination the lower limit of determination is 0.003 μg Hg. (M.K.)

  4. Methodological developments and applications of neutron activation analysis

    International Nuclear Information System (INIS)

    Kucera, J.

    2007-01-01

    The paper reviews the author's experience acquired and achievements made in methodological developments of neutron activation analysis (NAA) of mostly biological materials. These involve epithermal neutron activation analysis, radiochemical neutron activation analysis using both single- and multi-element separation procedures, use of various counting modes, and the development and use of the self-verification principle. The role of NAA in the detection of analytical errors is discussed and examples of applications of the procedures developed are given. (author)

  5. A QUANTITATIVE EVALUATION OF THE WATER DISTRIBUTION IN A SOIL SAMPLE USING NEUTRON IMAGING

    Directory of Open Access Journals (Sweden)

    Jan Šácha

    2016-10-01

    Full Text Available This paper presents an empirical method by Kang et al. recently proposed for correcting two-dimensional neutron radiography for water quantification in soil. The method was tested on data from neutron imaging of the water infiltration in a soil sample. The raw data were affected by neutron scattering and by beam hardening artefacts. Two strategies for identifying the correction parameters are proposed in this paper. The method has been further developed for the case of three-dimensional neutron tomography. In a related experiment, neutron imaging is used to record ponded-infiltration experiments in two artificial soil samples. Radiograms, i.e., two-dimensional projections of the sample, were acquired during infiltration. A calculation was made of the amount of water and its distribution within the radiograms, in the form of two-dimensional water thickness maps. Tomograms were reconstructed from the corrected and uncorrected water thickness maps to obtain the 3D spatial distribution of the water content within the sample. Without the correction, the beam hardening and the scattering effects overestimated the water content values close to the perimeter of the sample, and at the same time underestimated the values close to the centre of the sample. The total water content of the entire sample was the same in both cases. The empirical correction method presented in this study is a relatively accurate, rapid and simple way to obtain the quantitatively determined water content from two-dimensional and three-dimensional neutron images. However, an independent method for measuring the total water volume in the sample is needed in order to identify the correction parameters.

  6. Neutron activation analysis: Modelling studies to improve the neutron flux of Americium-Beryllium source

    Energy Technology Data Exchange (ETDEWEB)

    Didi, Abdessamad; Dadouch, Ahmed; Tajmouati, Jaouad; Bekkouri, Hassane [Advanced Technology and Integration System, Dept. of Physics, Faculty of Science Dhar Mehraz, University Sidi Mohamed Ben Abdellah, Fez (Morocco); Jai, Otman [Laboratory of Radiation and Nuclear Systems, Dept. of Physics, Faculty of Sciences, Tetouan (Morocco)

    2017-06-15

    Americium–beryllium (Am-Be; n, γ) is a neutron emitting source used in various research fields such as chemistry, physics, geology, archaeology, medicine, and environmental monitoring, as well as in the forensic sciences. It is a mobile source of neutron activity (20 Ci), yielding a small thermal neutron flux that is water moderated. The aim of this study is to develop a model to increase the neutron thermal flux of a source such as Am-Be. This study achieved multiple advantageous results: primarily, it will help us perform neutron activation analysis. Next, it will give us the opportunity to produce radio-elements with short half-lives. Am-Be single and multisource (5 sources) experiments were performed within an irradiation facility with a paraffin moderator. The resulting models mainly increase the thermal neutron flux compared to the traditional method with water moderator.

  7. Determination of arsenic in some Myanmar indigenous medicines by neutron activation analysis

    International Nuclear Information System (INIS)

    Myint, U.; Than, W.; Htay, H.; Myint, K.O.

    1994-01-01

    Am(Be) neutron source was used for activation of samples and 76 As radioactivity measured by both β- and γ-counting techniques. The samples analyzed were raw materials traditionally used in formulating Myanmar indigenous medicines. The results were compared with those obtained by volumetric analysis and those reported in the literature. (author) 4 refs.; 5 tabs

  8. Determination of arsenic in some Myanmar indigenous medicines by neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Myint, U; Than, W; Htay, H; Myint, K O [Yangon Univ. (Myanmar). Dept. of Chemistry

    1994-08-01

    Am(Be) neutron source was used for activation of samples and [sup 76]As radioactivity measured by both [beta]- and [gamma]-counting techniques. The samples analyzed were raw materials traditionally used in formulating Myanmar indigenous medicines. The results were compared with those obtained by volumetric analysis and those reported in the literature. (author) 4 refs.; 5 tabs.

  9. Study of irradiation damage by fast neutrons in samples of Portland cement

    International Nuclear Information System (INIS)

    Lucki, G.; Rosa Junior, A.A.

    1984-01-01

    The effect of neutron irradiation in samples of Portland cement was evaluated, using the resonance frequency method and pulse velocity of ultra-sound techniques. The samples were divided in three groups: 1) monitoring samples; 2) samples submitted to gamma heating; 3) Irradiated samples. In the sample preparation, it was used the Portland Santa Rita CP 320 cement, and water-cement rate of 0.40 l/Kg. The irradiation was done in the research reactor IEA-R1, at IPEN - CNEN/SP, with an integrated flux of 7.2 x 10 18 n/cm 2 (E approx. 1 MeV). Some damage were detected, due to the neutron flux, and by the thermal effect of gamma heating. (E.G.) [pt

  10. A review of conventional explosives detection using active neutron interrogation

    International Nuclear Information System (INIS)

    Whetstone, Z.D.; Kearfott, K.J.

    2014-01-01

    Conventional explosives are relatively easy to obtain and may cause massive harm to people and property. There are several tools employed by law enforcement to detect explosives, but these can be subverted. Active neutron interrogation is a viable alternative to those techniques, and includes: fast neutron analysis, thermal neutron analysis, pulsed fast/thermal neutron analysis, neutron elastic scatter, and fast neutron radiography. These methods vary based on neutron energy and radiation detected. A thorough review of the principles behind, advantages, and disadvantages of the different types of active neutron interrogation is presented. (author)

  11. Determination of manganese in blood by neutron activation analysis

    International Nuclear Information System (INIS)

    Kocsis, E.; Kovats, M.; Molnar, M.

    1981-01-01

    A new method has been elaborated: the manganese content of a blood sample was precipitated by H 2 O 2 , and analysed by neutron activation analysis. The mean value was 2.67x10 -8 g/g in men, 3.25x10 -8 g/g in women and 3.57x10 -8 g/g in men working as welders for several years. (L.E.)

  12. Trace elemental characterisation of different Indian tea samples by instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Lagad, Rupali A.; Alamelu, D.; Aggarwal, S.K.; Acharya, R.

    2010-01-01

    Determination of elemental content of different food materials is of importance since excess or deficiency of some of the elements have direct consequence to health of human beings. Tea is a common beverage consumed widely in India. India is one of the major country where good quality tea is produced. The tea plants are grown over a wide region of the country. It was of interest to study the elemental composition in tea samples from different geographical locations and to develop a suitable methodology to identify the geographical origin from the trace element profiles. With this objective, about 40 tea samples (both from plantations as well as from market) from the different locations in India viz. Assam, Munnar, Himachal Pradesh and Darjeeling were analyzed by INAA. About 150 mg of each of the sample packed in aluminium foil was irradiated in the self serve position of CIRUS reactor, BARC, for 3 to 5 hours at a neutron flux of ∼10 13 cm -2 s -1 . Along with the samples, Certified Reference Materials (CRMs) GBS-7(Tea leaves, as reference standard) and SRM-1515 (Apple leaves as control sample) were irradiated. Radioactive assay of the irradiated samples were carried out using a 40% relative efficiency HPGe detector coupled to 8K MCA and gamma-ray spectra were recorded for sufficient time for obtaining good counting statistics. Peak areas were determined using a peak-fit software PHAST. Concentrations of the different elements in tea samples were determined using relative method of INAA

  13. Improvements of neutron activation techniques for the determination of fissile material concentrations

    International Nuclear Information System (INIS)

    Papadopoulos, N.N.

    1987-01-01

    Certain experimental improvements, as variable sample size and irradiation position, automation and flexibility in radiation detection, broaden the measurable concentration range, increase the possible rate and accuracy of analysis and enlarge the application range of home-made nuclear analyzer for fissile material analysis by delayed fission neutron counting and for short-lived multielement analysis by neutron activation gamma-ray spectrometry. Intercomparisons of results by various methods and laboratories show the need for regular checks of techniques to ensure reliable measurements. (author)

  14. Determination of Oxygen in Aluminum by Means of 14 MeV Neutrons with an Account of Flux Attenuation in the Sample

    Energy Technology Data Exchange (ETDEWEB)

    Brune, D; Jirlow, K

    1967-11-15

    This study concerns the determination of oxygen present at low levels in aluminum using the 14 MeV neutron activation technique. The sensitivity obtained amounted to 0.2 mg oxygen. Various nuclear methods for the oxygen determination have been briefly reviewed. The attenuation of fast neutrons inside the aluminum samples has been calculated.

  15. Two specialized delayed-neutron detector designs for assays of fissionable elements in water and sediment samples

    International Nuclear Information System (INIS)

    Balestrini, S.J.; Balagna, J.P.; Menlove, H.O.

    1976-01-01

    Two specialized neutron-sensitive detectors are described which are employed for rapid assays of fissionable elements by sensing for delayed neutrons emitted by samples after they have been irradiated in a nuclear reactor. The more sensitive of the two detectors, designed to assay for uranium in water samples, is 40% efficient; the other, designed for sediment sample assays, is 27% efficient. These detectors are also designed to operate under water as an inexpensive shielding against neutron leakage from the reactor and neutrons from cosmic rays. (Auth.)

  16. Characterisation of South African coals using instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    Hart, R.J.

    1985-01-01

    This report includes the establishment of the major minor and trace element compositions of South African coals with the aim of characterising the different coal seams within a basin, defining regions of similar compositions and obtaining an overall view of the geochemistry of coals in this country. The results of 40 coal samples analysed by neutron activation analysis

  17. Study on bioavailability of zinc for children's diet by using activable isotopic tracer 70Zn and neutron activation analysis techniques

    International Nuclear Information System (INIS)

    Zhang Yangmei; Ni Bangfa; Wang Pingsheng; Tian Weizhi; Cao Lei

    2001-01-01

    Bioavailability of zinc for three groups (low amount of diet zinc, balance amount of diet zinc and high amount of diet zinc) of children's diet is studied by using activable isotopic tracer 70 Zn and neutron activation analysis techniques. The results indicate that the fractional absorption of zinc from balance diet zinc group is the highest, up to 33.9%. A procedure of pre-irradiation concentration zinc for fecal samples using anion exchanger is developed, and the enriched 70 Zn with isotopic abundance of 18.3% is used for tracer. The mass ratios between 70 Zn and 68 Zn or 64 Zn and their contents between natural zinc and enriched zinc are used to calculate the bioavailability of zinc. Instrumental neutron activation analysis of 64 Zn of each original fecal samples and pre-irradiation concentrated zinc samples are used to normalize the chemical yield in order to reduce the uncertainty during the chemical separation procedure

  18. Evaluation of precision and accuracy of neutron activation analysis method of environmental samples analysis

    International Nuclear Information System (INIS)

    Wardani, Sri; Rina M, Th.; L, Dyah

    2000-01-01

    Evaluation of precision and accuracy of Neutron Activation Analysis (NAA) method used by P2TRR performed by analyzed the standard reference samples from the National Institute of Environmental Study of Japan (NIES-CRM No.10 (rice flour) and the National Bureau of USA (NBS-SRM 1573a (tomato leave) by NAA method. In analyze the environmental SRM No.10 by NAA method in qualitatively could identified multi elements of contents, namely: Br, Ca, Co, CI, Cs, Gd, I, K< La, Mg, Mn, Na, Pa, Sb, Sm, Sr, Ta, Th, and Zn (19 elements) for SRM 1573a; As, Br, Cr, CI, Ce, Co, Cs, Fe, Ga, Hg, K, Mn, Mg, Mo, Na, Ni, Pb, Rb, Sr, Se, Sc, Sb, Ti, and Zn, (25 elements) for CRM No.10a; Ag, As, Br, Cr, CI, Ce, Cd, Co, Cs, Eu, Fe, Ga, Hg, K, Mg, Mn, Mo, Na, Nb, Pb, Rb, Sb, Sc, Th, TI, and Zn, (26 elements) for CRM No. 10b; As, Br, Co, CI, Ce, Cd, Ga, Hg, K, Mn, Mg, Mo, Na, Nb, Pb, Rb, Sb, Se, TI, and Zn (20 elementary) for CRM No.10c. In the quantitatively analysis could determined only some element of sample contents, namely: As, Co, Cd, Mo, Mn, and Zn. From the result compared with NIES or NBS values attained with deviation of 3% ∼ 15%. Overall, the result shown that the method and facilities have a good capability, but the irradiation facility and the software of spectrometry gamma ray necessary to developing or seriously research perform

  19. Measurements of DT and DD neutron yields by neutron activation on TFTR

    International Nuclear Information System (INIS)

    Barnes, C.W.; Larson, A.R.; LeMunyan, G.

    1994-01-01

    A variety of elemental foils have been activated by neutron fluence from TFTR under conditions with the DT neutron yield per shot ranging from 10 12 to over 10 18 , and with the DT/(DD+DT) neutron ratio varying from 0.5% (from triton burnup) to unity. Linear response over this large dynamic range is obtained by reducing the mass of the foils and increasing the cooling time, all while accepting greatly improved counting statistics. Effects on background gamma-ray lines from foil-capsule-material contaminants. and the resulting lower limits on activation foil mass, have been determined. DT neutron yields from dosimetry standard reactions on aluminum, chromium, iron, nickel, zirconium, and indium are in agreement within the ±9% (one-sigma,) accuracy of the measurements: also agreeing are yields from silicon foils using the ACTL library cross-section. While the ENDF/B-V library has too low a cross-section. Preliminary results from a variety of other threshold reactions are presented. Use of the 115 In(n,n) 115m In reaction (0.42 times as sensitive to DT neutrons as DD neutrons) in conjunction with pure-DT reactions allows a determination of the DT/(DD+DT) ratio in trace tritium or low-power tritium beam experiments

  20. Measurements of DT and DD neutron yields by neutron activation on TFTR

    International Nuclear Information System (INIS)

    Barnes, C.W.; Larson, A.R.; LeMunyan, G.

    1995-03-01

    A variety of elemental foils have been activated by neutron fluence from TFTR under conditions with the DT neutron yield per shot ranging from 10 12 to over 10 18 , and with the DT/(DD+DT) neutron ratio varying from 0.5% (from triton burnup) to unity. Linear response over this large dynamic range is obtained by reducing the mass of the foils and increasing the cooling time, all while accepting greatly improved counting statistics. Effects on background gamma-ray lines from foil-capsule-material contaminants, and the resulting lower limits on activation foil mass, have been determined. DT neutron yields from dosimetry standard reactions on aluminum, chromium, iron, nickel, zirconium, and indium are in agreement within the ±9% (one-sigma) accuracy of the measurements; also agreeing are yields from silicon foils using the ACTL library cross-section, while the ENDF/B-V library has too low a cross-section. Preliminary results from a variety of other threshold reactions are presented. Use of the 115 In(n.n') 115m In reaction (0.42 times as sensitive to DT neutrons as DD neutrons) in conjunction with pure-DT reactions allows a determination of the DT/(DD+DT) ratio in trace tritium or low-power tritium beam experiments

  1. 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

  2. Virtual sampling in variational processing of Monte Carlo simulation in a deep neutron penetration problem

    International Nuclear Information System (INIS)

    Allagi, Mabruk O.; Lewins, Jeffery D.

    1999-01-01

    In a further study of virtually processed Monte Carlo estimates in neutron transport, a shielding problem has been studied. The use of virtual sampling to estimate the importance function at a certain point in the phase space depends on the presence of neutrons from the real source at that point. But in deep penetration problems, not many neutrons will reach regions far away from the source. In order to overcome this problem, two suggestions are considered: (1) virtual sampling is used as far as the real neutrons can reach, then fictitious sampling is introduced for the remaining regions, distributed in all the regions, or (2) only one fictitious source is placed where the real neutrons almost terminate and then virtual sampling is used in the same way as for the real source. Variational processing is again found to improve the Monte Carlo estimates, being best when using one fictitious source in the far regions with virtual sampling (option 2). When fictitious sources are used to estimate the importances in regions far away from the source, some optimization has to be performed for the proportion of fictitious to real sources, weighted against accuracy and computational costs. It has been found in this study that the optimum number of cells to be treated by fictitious sampling is problem dependent, but as a rule of thumb, fictitious sampling should be employed in regions where the number of neutrons from the real source fall below a specified limit for good statistics

  3. Activation analysis of gold in geological samples (Paper No. RA-24)

    International Nuclear Information System (INIS)

    Das, N.R.; Bhattacharyya, S.N.

    1990-02-01

    The technique of neutron activation analysis (NAA) has been applied to study the distribution of gold in some geological samples. Traces of gold in the samples were preconcentrated in a solid matrix through a chemical procedure involving solvent extraction using MIBK and coprecipitation with PbS. Gold contents in the samples as determined by NAA vary from ppb to ppm levels. (author)

  4. Analysis of human enamel and dentine by neutron activation analysis; Analise de esmalte e dentina de humanos pelo metodo de ativacao com neutrons

    Energy Technology Data Exchange (ETDEWEB)

    Soares, Marco A.B. [Sao Paulo Univ., SP (Brazil). Inst. de Quimica]. E-mail: vankfire@gmail.com; Adachi, Eduardo M.; Saiki, Mitiko [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)

    2005-07-01

    Determination of trace elements in dental tissues has been of great interest to study the correlation between element composition and caries as well as food habits of individuals. In the present study dentine and enamel samples from healthy individuals were analysed by neutron activation analysis. The teeth were provided form dental clinics, and they were previously washed using purified water and acetone. Then they were dried at 40 deg C and ground in a agate mortar. The samples and element standards were irradiated with thermal neutrons at the IEA-R1 nuclear reactor. Long irradiations of 8 h under thermal neutron flux of 5x10{sup 12} n cm{sup -2} s{sup -1} were used for Ca, Na, Sr and Zn determinations. In short irradiations of 15 s and under neutron flux of 10{sup 12} n cm{sup -2} s{sup -1} the elements Mg, Mn, Na e Sr were determined. The induced gamma activities of the samples and standards were measured using a hyperpure Ge detector coupled to a gamma ray spectrometer. Elemental concentrations were calculated by comparative method. Results obtained showed that Ca, Mg and Na are present in both tissues at the level of percentages and the elements Mn, Sr and Zn at the {mu}g g{sup -1} levels. For quality control of the results the certified reference materials NIST 1400 Bone Ash and NIST 1486 Bone Meal were analysed. (author)

  5. Preparation and characterisation of magnetic nanostructured samples for inelastic neutron scattering experiments

    Energy Technology Data Exchange (ETDEWEB)

    Kreuzpaintner, Wolfgang

    2010-06-22

    Recent advances in thin-film structuring techniques have generated significant interest in the dynamics of spin waves in magnetic nanostructures and the possible use of inelastic neutron scattering (INS) for their investigation. This thesis describes the design and implementation, at GKSS Research Centre, of equipment for preparation of large and laterally submicron and nanometre structured magnetic samples for such future INS experiments. After a brief resume on spin waves in nanostructures, the development work on new purpose-designed equipment, including high vacuum (HV) argon ion beam milling and ultra high vacuum (UHV) e-beam evaporation setups, is described. Ni nanodot as well as Ni and novel Gd nanowire samples were prepared using combinations of sputter deposition, laser interference lithography, argon ion beam milling, e-beam evaporation and self organisation techniques. With reference to sample preparation, epitaxial growth studies for Ni on Si(100) substrate were performed, resulting in the development of a new deposition process, which by thermal tuning allows for the direct epitaxial growth of Ni on Si with unprecedented crystalline quality. The results of various characterisation experiments on the prepared nanostructured samples, including Scanning Electron Microscopy (SEM), microprobe analysis, Atomic and Magnetic Force Microscopy (AFM/MFM), Vibrating Sample Magnetometry (VSM), X-ray Diffraction (XRD) and Reflectivity (XRR), unpolarised and Polarised Neutron Scattering (PNR) and off-specular scattering by X-rays and neutrons using rocking scans and Time-Of-Flight Grazing Incidence Small Angle Neutron Scattering (TOF-GISANS), together with various analysis procedures such as Distorted-Wave Born Approximation (DWBA), are reported. The analysis of a Gd nanowire sample by TOF-GISANS led to a novel evaluation technique which in comparison with single wavelength methods allows portions of reciprocal space to be scanned without changing the angle of

  6. Preparation and characterisation of magnetic nanostructured samples for inelastic neutron scattering experiments

    International Nuclear Information System (INIS)

    Kreuzpaintner, Wolfgang

    2010-01-01

    Recent advances in thin-film structuring techniques have generated significant interest in the dynamics of spin waves in magnetic nanostructures and the possible use of inelastic neutron scattering (INS) for their investigation. This thesis describes the design and implementation, at GKSS Research Centre, of equipment for preparation of large and laterally submicron and nanometre structured magnetic samples for such future INS experiments. After a brief resume on spin waves in nanostructures, the development work on new purpose-designed equipment, including high vacuum (HV) argon ion beam milling and ultra high vacuum (UHV) e-beam evaporation setups, is described. Ni nanodot as well as Ni and novel Gd nanowire samples were prepared using combinations of sputter deposition, laser interference lithography, argon ion beam milling, e-beam evaporation and self organisation techniques. With reference to sample preparation, epitaxial growth studies for Ni on Si(100) substrate were performed, resulting in the development of a new deposition process, which by thermal tuning allows for the direct epitaxial growth of Ni on Si with unprecedented crystalline quality. The results of various characterisation experiments on the prepared nanostructured samples, including Scanning Electron Microscopy (SEM), microprobe analysis, Atomic and Magnetic Force Microscopy (AFM/MFM), Vibrating Sample Magnetometry (VSM), X-ray Diffraction (XRD) and Reflectivity (XRR), unpolarised and Polarised Neutron Scattering (PNR) and off-specular scattering by X-rays and neutrons using rocking scans and Time-Of-Flight Grazing Incidence Small Angle Neutron Scattering (TOF-GISANS), together with various analysis procedures such as Distorted-Wave Born Approximation (DWBA), are reported. The analysis of a Gd nanowire sample by TOF-GISANS led to a novel evaluation technique which in comparison with single wavelength methods allows portions of reciprocal space to be scanned without changing the angle of

  7. On-line neutron activation analyzers

    International Nuclear Information System (INIS)

    Flahaut, V.; Colmon, A.

    1999-01-01

    A neutronic analyser has been designed to determine the composition of the flow of raw materials entering a cement factory on the conveyor belt. This new system gives a reliable analysis of the whole cargo that outdates the sampling or the usual surface analysis based on fluorescence spectrometry. The accuracy is about 1%.The neutrons interact with the materials on an average depth of 25 cm and are absorbed by nuclei, these nuclei produce photons whose energy is characteristic of the chemical element itself. The composition can be deduced by measuring the number of photons emitted and their energy. The analysis is made on-line and can concern the search for about 10 compounds. In the case of cement the list of compounds is: SiO 2 , CaO, Al 2 O 3 , Fe 2 O 3 , MgO, Na 2 O, TiO 2 , S, Mn 2 O 3 , K 2 O, and H 2 O. The neutron generator involves a deuterium ion source whose deuterium ions are accelerated by means of an electrical field and impinge on a tritiated target, the nuclear reactions between deuterium and tritium produce 14 MeV neutrons. This neutron analysing technique can be adapted to any need of on-line composition determination. (A.C.)

  8. Determination of Substances Content of Soil Surface Using Fast Neutron Activation Analysis

    International Nuclear Information System (INIS)

    Elin Nuraini; Elisabeth; Sunardi

    2002-01-01

    Determination of substances content of soil surface using neutron activation analysis has been performed. The aim of this research is to determine whether there are any dangerous, hazardous and toxic substances that released from The Research and Development Center for Advanced Technology (RDCAT) as a government institution has possibility in releasing that substances to the environment by surface water, sewage or rain water that give any dangerous the environmental. The fast neutron activation analysis was used to analyze the type and concentration of substances qualitative and quantitatively. The quantitative analysis was performed using relative method. Samples were counted using NaI(TI) detector. The result showed that there are several substances such as Mn-55, Fe-56, P-31, Al-27. Zn,65 and Mg-24. And there are found any hazardous, dangerous and toxic substances in the samples that causing any danger to human and environment. (author)

  9. Pulsed neutron generator for mass flow measurement using the pulsed neutron activation technique

    International Nuclear Information System (INIS)

    Rochau, G.E.; Hornsby, D.R.; Mareda, J.F.; Riggan, W.C.

    1980-01-01

    A high-output, transportable neutron generator has been developed to measure mass flow velocities in reactor safety tests using the Pulsed Neutron Activation (PNA) Technique. The PNA generator produces >10 10 14 MeV D-T neutrons in a 1.2 millisecond pulse. The Millisecond Pulse (MSP) Neutron Tube, developed for this application, has an expected operational life of 1000 pulses, and it limits the generator pulse repetition rate to 12 pulses/minute. A semiconductor neutron detector is included in the generator package to monitor the neutron output. The control unit, which can be operated manually or remotely, also contains a digital display with a BCD output for the neutron monitor information. The digital logic of the unit controls the safety interlocks and rejects transient signals which could accidently fire the generator

  10. Neutron activation analysis of trace elements in foodstuffs

    International Nuclear Information System (INIS)

    Schelenz, R.; Bayat, I.; Fischer, E.

    1976-05-01

    For the determination of trace elements in foodstuffs with the aid of neutron activation analysis the separation of volatile radionuclides after digestion of the sample is of special interest for radiochemical processing. A distillation procedure was developed to give reproducable results, however optimal conditions were not found for all volatile radionuclides studied. The required selective separation of Br-82 from the distillate was best achieved by the application of an ion-exchange column-chromatography technique. The computer programs for the evaluation of complex gamma spectra have been developed further. The automatic peak search and peak area determination is based on a computer program using the correlation technique and carried out with a mini-computer coupled with a multi-channel gamma spectrometer. The results, which are presented in 3 earlier reports relating to this research program, reveal the advantages and disadvantages of the individual steps of the radiochemical separation scheme. Before neutron activation analysis can be introduced on a routine basis, some aspects of the radiochemical process remain to be tested; these studies will be published in a fourth and final report. (orig.) [de

  11. Trace element concentrations in human bone using instrumental neutron activation analysis

    International Nuclear Information System (INIS)

    El-Amri, F.A.; El-Kabroun, M.A.R.

    1997-01-01

    Instrumental neutron activation analysis has been applied to analyze 23 bone samples obtained from Libyan patient aged (3-80) years for the study of the concentration levels of trace elements Ba, Br, Ca, Fe, Sr and Zn and their concentration patterns regarding to the age and sex of the patients. (author)

  12. Multi elementary analysis in medicinal plants through the neutron activation method

    International Nuclear Information System (INIS)

    Vaz, M.S.; Saiki, M.; Vasconcellos, M.B.A.; Sertie, J.A.A.

    1990-01-01

    A instrumental method by neutron activation in multielementary analysis was applied. Samples of Centelha asiatica (Cairucu) and Paulinia cupana (Guarana) were used. The elements Al, Br, Ca, Cl, Fe, K, Mn, Na, Rb, Sc, and Zn were determined. The results like precision and exactitude were analysed. (L.M.J.) [pt

  13. 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)

  14. The application of radiotracer technique for preconcentration neutron activation analysis

    International Nuclear Information System (INIS)

    Wang Xiaolin; Chen Yinliang; Sun Ying; Fu Yibei

    1995-01-01

    The application of radiotracer technique for preconcentration neutron activation analysis (Pre-NAA) are studied and the method for determination of chemical yield of Pre-NAA is developed. This method has been applied to determination of gold, iridium and rhenium in steel and rock samples and the contents of noble metal are in the range of 1-20 ng·g -1 (sample). In addition, the accuracy difference caused by determination of chemical yield between RNAA and Pre-NAA are also discussed

  15. Application of neutron activation analysis method on biomonitors for assessing environment quality

    International Nuclear Information System (INIS)

    Nitescu, E. A.; Valeca, S.; Bucsa, A. F.

    2016-01-01

    The purpose of this paper is to determine the chemical elements concentrations which affect both the population health and environment, such as toxic agents which are contained in air and are retained by precipitation inside the biomonitors vegetal tissues. The Neutron Activation Analysis is an analytic technique based on measuring the numbers and the energy of gamma radiation emitted by the radioactive isotopes produced in the sample matrix by irradiation with thermal neutrons in a nuclear reactor [1]. Usually, the samples are irradiated together with specific neutron flux monitors, duplicates and interest elements standards for a prior selected period of time inside the core of nuclear reactor. After the irradiation experiment and the specific radioactive decaying, can proceed measuring the gamma energies spectrum by using a high resolution detection system (HPGe - High Purity Germanium crystal) for gamma spectrometry and then assess the impact of the traced elements on population and environment. (authors)

  16. Neutron activation analysis of limestone objects

    International Nuclear Information System (INIS)

    Meyers, P.; Van Zelst, L.

    1977-01-01

    The elemental composition of samples from limestone objects were determined by neutron activation analysis to investigate whether this technique can be used to distinguish between objects made of limestone from different sources. Samples weighing between 0.2-2 grams were obtained by drilling from a series of ancient Egyptian and medieval Spanish objects. Analysis was performed on aliquots varying in weight from 40-100 milligrams. The following elements were determined quantitatively: Na, K, Rb, Cs, Ba, Sc, La, Ce, Sm, Eu, Hf, Th, Ta, Cr, Mn, Fe, Co and Zn. The data on Egyptian limestones indicate that, because of the inhomogeneous nature of the stone, 0.2-2 gram samples may not be representative of an entire object. Nevertheless, multivariate statistical methods produced a clear distinction between objects originating from the Luxor area (ancient Thebes) and objects found north of Luxor. The Spanish limestone studied appeared to be more homogeneous. Samples from stylistically related objects have similar elemental compositions while relative large differences were observed between objects having no relationship other than the common provenance of medieval Spain. (orig.) [de

  17. The influence of neutron activated products in BIXS method for tungsten

    International Nuclear Information System (INIS)

    Yang, Yang; Peng, Taiping; Chen, Zhilin; Zhang, Zhe; Song, Honghu

    2016-01-01

    Highlights: • An approach is proposed to assess the influence of neutron activated products in BIXS method for tungsten based on Monte Carlo simulations. • Six principal radioactive neutron activated products (W-181, W-185, W-187, Ta-182, Re-186 and Re-188) with exhaustive decay data were included in the calculation to simulate the real condition. • W-187 strongly affects the tritium measurement shortly after DT experiments and about one month later W-181, W-185 and Ta-182 dominate the effects of neutron activated products. • The intensity of spectrum devoted by NAPs is as much as 10.6 times larger than by tritium in the same region of interest (ROI) directly after reactor shutdown, while it will reduce to 0.83% after 19 months. - Abstract: Tritium β-decay Induced X-ray Spectroscopy (BIXS) is a promising method to obtain tritium retention details both on surface and in bulk of plasma facing materials (PFMs) in magnetic fusion devices. Influence of neutron activated products (NAPs) is one of the primary problems in BIXS, since the energy of Compton scattering photons and characteristic X-rays is close to the range of tritium β-rays. In this paper, Monte Carlo simulation was introduced to evaluate effects of NAPs in BIXS measurements for tungsten. Three steps are included in simulation, neutron flux simulation to reckon the neutron flux in PFMs based on the simplified model of ITER, activated products calculation to compute the distribution of NAPs in PFMs and radiation spectra simulation to calculate the spectra of NAPs in PFMs sample. Six typical nuclides (including W-185, W-181 and Re-188, etc.) produced by neutron irradiation were considered in this study. Finally, influence of NAPs was estimated quantitatively with the assumption that 1% of DT fuel retained in PFMs uniformly. It is found that the intensity of spectrum devoted by NAPs is as much as 10.6 times larger than it by tritium in the same region of interest (ROI) directly after reactor shutdown

  18. The influence of neutron activated products in BIXS method for tungsten

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Yang; Peng, Taiping, E-mail: yangyanginpc@163.com; Chen, Zhilin; Zhang, Zhe; Song, Honghu

    2016-12-15

    Highlights: • An approach is proposed to assess the influence of neutron activated products in BIXS method for tungsten based on Monte Carlo simulations. • Six principal radioactive neutron activated products (W-181, W-185, W-187, Ta-182, Re-186 and Re-188) with exhaustive decay data were included in the calculation to simulate the real condition. • W-187 strongly affects the tritium measurement shortly after DT experiments and about one month later W-181, W-185 and Ta-182 dominate the effects of neutron activated products. • The intensity of spectrum devoted by NAPs is as much as 10.6 times larger than by tritium in the same region of interest (ROI) directly after reactor shutdown, while it will reduce to 0.83% after 19 months. - Abstract: Tritium β-decay Induced X-ray Spectroscopy (BIXS) is a promising method to obtain tritium retention details both on surface and in bulk of plasma facing materials (PFMs) in magnetic fusion devices. Influence of neutron activated products (NAPs) is one of the primary problems in BIXS, since the energy of Compton scattering photons and characteristic X-rays is close to the range of tritium β-rays. In this paper, Monte Carlo simulation was introduced to evaluate effects of NAPs in BIXS measurements for tungsten. Three steps are included in simulation, neutron flux simulation to reckon the neutron flux in PFMs based on the simplified model of ITER, activated products calculation to compute the distribution of NAPs in PFMs and radiation spectra simulation to calculate the spectra of NAPs in PFMs sample. Six typical nuclides (including W-185, W-181 and Re-188, etc.) produced by neutron irradiation were considered in this study. Finally, influence of NAPs was estimated quantitatively with the assumption that 1% of DT fuel retained in PFMs uniformly. It is found that the intensity of spectrum devoted by NAPs is as much as 10.6 times larger than it by tritium in the same region of interest (ROI) directly after reactor shutdown

  19. Measurement of trace cadmium and elements in bone by epithermal neutron activation analysis

    International Nuclear Information System (INIS)

    Dowlati, R.; Jervis, R.E.

    1991-01-01

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

  20. Determinations of elements in pepperbush standard reference material by neutron activation and X-ray fluorescence analyses

    International Nuclear Information System (INIS)

    Mizumoto, Yoshihiko; Okada, Takayuki; Tatsumi, Toshiya; Kusakabe, Toshio; Katsurayama, Kousuke; Iwata, Shiro.

    1988-01-01

    Elemental contents in Pepperbush standard reference material have been determined by neutron activation and X-ray fluorescence analyses. The standard samples of orchard leaves, tomato leaves, pine needles and Kale are used for the experiment. In the neutron activation analysis, gamma-ray spectra of nuclei produced by (n,γ) reaction on Pepperbush and standard samples are measured with Ge detectors. In the X-ray fluorescence analysis, the samples are excited with X-rays from X-ray tube with rhodium anode, and the characteristic X-rays from samples are measured with a proportional counter or NaI(Tl) detector. From the gamma- and X-ray intensities, the elemental contents in Pepperbush are determined. As a result, the contents of seventeen elements, such as sodium, calcium, iron, etc., in Pepperbush are determined. (author)