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

International Nuclear Information System (INIS)

Sepulveda Munita, C.J.A.

1979-01-01

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

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)

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.

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)

Activation analysis of Al2O3 samples at the RB reactor

International Nuclear Information System (INIS)

Sokcic-Kostic, M.; Antic, D.; Pesic, M.

1994-01-01

Low flux activation analysis was successfully performed at the zero power RB reactor on a specific sample giving good results. For analysis of low concentration, isotopes must have cross sections of a few barns and periods of a few days with profitable disintegration schemes. This means irradiation of n x ∼ 10 min and flux n x 10 7 n/cm 2 s. The specific results of this and similar experiments provide information for industrial treatment of trace elements and sample analyses in different fields of research as well as food sample analysis

Development of digital gamma-activation autoradiography for analysis of samples of large area

International Nuclear Information System (INIS)

Kolotov, V.P.; Grozdov, D.S.; Dogadkin, N.N.; Korobkov, V.I.

2011-01-01

Gamma-activation autoradiography is a prospective method for screening detection of inclusions of precious metals in geochemical samples. Its characteristics allow analysis of thin sections of large size (tens of cm2), that favourably distinguishes it among the other methods for local analysis. At the same time, the activating field of the accelerator bremsstrahlung, displays a sharp intensity decrease relative to the distance along the axis. A method for activation dose ''equalization'' during irradiation of the large size thin sections has been developed. The method is based on the usage of a hardware-software system. This includes a device for moving the sample during the irradiation, a program for computer modelling of the acquired activating dose for the chosen kinematics of the sample movement and a program for pixel-by pixel correction of the autoradiographic images. For detection of inclusions of precious metals, a method for analysis of the acquired dose dynamics during sample decay has been developed. The method is based on the software processing pixel by pixel a time-series of coaxial autoradiographic images and generation of the secondary meta-images allowing interpretation regarding the presence of interesting inclusions based on half-lives. The method is tested for analysis of copper-nickel polymetallic ores. The developed solutions considerably expand the possible applications of digital gamma-activation autoradiography. (orig.)

Development of digital gamma-activation autoradiography for analysis of samples of large area

Energy Technology Data Exchange (ETDEWEB)

Kolotov, V.P.; Grozdov, D.S.; Dogadkin, N.N.; Korobkov, V.I. [Russian Academy of Sciences, Moscow (Russian Federation). Vernadsky Inst. of Geochemistry and Analytical Chemistry

2011-07-01

Gamma-activation autoradiography is a prospective method for screening detection of inclusions of precious metals in geochemical samples. Its characteristics allow analysis of thin sections of large size (tens of cm2), that favourably distinguishes it among the other methods for local analysis. At the same time, the activating field of the accelerator bremsstrahlung, displays a sharp intensity decrease relative to the distance along the axis. A method for activation dose ''equalization'' during irradiation of the large size thin sections has been developed. The method is based on the usage of a hardware-software system. This includes a device for moving the sample during the irradiation, a program for computer modelling of the acquired activating dose for the chosen kinematics of the sample movement and a program for pixel-by pixel correction of the autoradiographic images. For detection of inclusions of precious metals, a method for analysis of the acquired dose dynamics during sample decay has been developed. The method is based on the software processing pixel by pixel a time-series of coaxial autoradiographic images and generation of the secondary meta-images allowing interpretation regarding the presence of interesting inclusions based on half-lives. The method is tested for analysis of copper-nickel polymetallic ores. The developed solutions considerably expand the possible applications of digital gamma-activation autoradiography. (orig.)

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)

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)

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

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)

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)

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

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.

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)

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

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)

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)

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

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)

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.

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)

The problem of large samples. An activation analysis study of electronic waste material

International Nuclear Information System (INIS)

Segebade, C.; Goerner, W.; Bode, P.

2007-01-01

Large-volume instrumental photon activation analysis (IPAA) was used for the investigation of shredded electronic waste material. Sample masses from 1 to 150 grams were analyzed to obtain an estimate of the minimum sample size to be taken to achieve a representativeness of the results which is satisfactory for a defined investigation task. Furthermore, the influence of irradiation and measurement parameters upon the quality of the analytical results were studied. Finally, the analytical data obtained from IPAA and instrumental neutron activation analysis (INAA), both carried out in a large-volume mode, were compared. Only parts of the values were found in satisfactory agreement. (author)

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

International Nuclear Information System (INIS)

Armelin, Maria Jose Aguirre

1978-01-01

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

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

Determination of chromium, cobalt and nickel in tissue samples by radiochemical activation analysis

International Nuclear Information System (INIS)

Reisell, A.; Lakomaa, E.L.

1983-03-01

A radiochemical neutron activation analysis method for the determination of chromium, cobalt and nickel in tissue samples. A radiochemical neutron activation analysis method for the determination of chromium, cobalt and nickel has been developed. The destruction device used consisted of a combined wet-ashing-distillation and ion-exchange system. Six samples could be treated at the same time. The samples were wet-ashed with H*L2SO*L4-H*L2O*L2 mixture. Volatile elements were distilled as bromide compounds with HBr*H-. The distillation residue in 8M HCl was passed through hydrated antimony pentoxide (HAP) in order to remove disturbing *H2*H4Na-activity and through a Dowex 2 x 8 column so as to retain *H6*H0Co (formed from *H5*H8Ni). Chromium was elutriated from the column and precipitated as Cr(OH)*L3 for the removal of disturbing *H3*H2P-activity. The standards and samples were treated in a similar manner each so that the yield determination is not necessarily needed. The yields by tracer experiments were (43 +- 5) % for Cr, (93 +- 4) % for Co and (88 +- 14) % for Ni. The precision and accuracy of the method were studied by using reference materials of the National Bureau of Standards (NBS) and the International Atomic Energy Agency (IAEA)

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.)

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)

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)

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

Quantitative portable gamma spectroscopy sample analysis for non-standard sample geometries

International Nuclear Information System (INIS)

Enghauser, M.W.; Ebara, S.B.

1997-01-01

Utilizing a portable spectroscopy system, a quantitative method for analysis of samples containing a mixture of fission and activation products in nonstandard geometries was developed. The method can be used with various sample and shielding configurations where analysis on a laboratory based gamma spectroscopy system is impractical. The portable gamma spectroscopy method involves calibration of the detector and modeling of the sample and shielding to identify and quantify the radionuclides present in the sample. The method utilizes the intrinsic efficiency of the detector and the unattenuated gamma fluence rate at the detector surface per unit activity from the sample to calculate the nuclide activity and Minimum Detectable Activity (MDA). For a complex geometry, a computer code written for shielding applications (MICROSHIELD) is utilized to determine the unattenuated gamma fluence rate per unit activity at the detector surface. Lastly, the method is only applicable to nuclides which emit gamma rays and cannot be used for pure beta emitters. In addition, if sample self absorption and shielding is significant, the attenuation will result in high MDA's for nuclides which solely emit low energy gamma rays. The following presents the analysis technique and presents verification results demonstrating the accuracy of the method

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

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.

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)

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)

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)

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)

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

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.

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.

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

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

Phase 1 sampling and analysis plan for the 304 Concretion Facility closure activities

International Nuclear Information System (INIS)

Adler, J.G.

1994-01-01

This document provides guidance for the initial (Phase 1) sampling and analysis activities associated with the proposed Resource Conservation and Recovery Act of 1976 (RCRA) clean closure of the 304 Concretion Facility. Over its service life, the 304 Concretion Facility housed the pilot plants associated with cladding uranium cores, was used to store engineering equipment and product chemicals, was used to treat low-level radioactive mixed waste, recyclable scrap uranium generated during nuclear fuel fabrication, and uranium-titanium alloy chips, and was used for the repackaging of spent halogenated solvents from the nuclear fuels manufacturing process. The strategy for clean closure of the 304 Concretion Facility is to decontaminate, sample (Phase 1 sampling), and evaluate results. If the evaluation indicates that a limited area requires additional decontamination for clean closure, the limited area will be decontaminated, resampled (Phase 2 sampling), and the result evaluated. If the evaluation indicates that the constituents of concern are below action levels, the facility will be clean closed. Or, if the evaluation indicates that the constituents of concern are present above action levels, the condition of the facility will be evaluated and appropriate action taken. There are a total of 37 sampling locations comprising 12 concrete core, 1 concrete chip, 9 soil, 11 wipe, and 4 asphalt core sampling locations. Analysis for inorganics and volatile organics will be performed on the concrete core and soil samples. Separate concrete core samples will be required for the inorganic and volatile organic analysis (VOA). Analysis for inorganics only will be performed on the concrete chip, wipe, and asphalt samples

Measurements of {sup 55}Fe activity in activated steel samples with GEMPix

Energy Technology Data Exchange (ETDEWEB)

Curioni, A. [CERN, 1211 Geneva 23 (Switzerland); Politecnico di Milano, Piazza Leonardo da Vinci 32, 20133 Milano (Italy); Dinar, N. [CERN, 1211 Geneva 23 (Switzerland); Université de Paris VII, 5 rue Thomas-Mann, 75013 Paris (France); La Torre, F.P. [CERN, 1211 Geneva 23 (Switzerland); Leidner, J., E-mail: johannes.leidner@cern.ch [CERN, 1211 Geneva 23 (Switzerland); RWTH Aachen, Templergraben 55, 52056 Aachen (Germany); Murtas, F. [CERN, 1211 Geneva 23 (Switzerland); INFN-LNF, Via E. Fermi 40, 00044 Frascati (Italy); Puddu, S.; Silari, M. [CERN, 1211 Geneva 23 (Switzerland)

2017-03-21

In this paper we present a novel method, based on the recently developed GEMPix detector, to measure the {sup 55}Fe content in samples of metallic material activated during operation of CERN accelerators and experimental facilities. The GEMPix, a gas detector with highly pixelated read-out, has been obtained by coupling a triple Gas Electron Multiplier (GEM) to a quad Timepix ASIC. Sample preparation, measurements performed on 45 samples and data analysis are described. The calibration factor (counts per second per unit specific activity) has been obtained via measurements of the {sup 55}Fe activity determined by radiochemical analysis of the same samples. Detection limit and sensitivity to the current Swiss exemption limit are calculated. Comparison with radiochemical analysis shows inconsistency for the sensitivity for only two samples, most likely due to underestimated uncertainties of the GEMPix analysis. An operative test phase of this technique is already planned at CERN.

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)

Qualitative Elemental Analyses of a Meteorite Sample Found in Turkey by Photo-activation Analysis Method

International Nuclear Information System (INIS)

Ertugay, C; Boztosun, I; Ozmen, S F; Dapo, H

2015-01-01

In this paper, a meteorite sample provided from TÜBITAK National Observatory found in Turkey has been investigated by using a clinical linear accelerator that has endpoint energy of 18 MeV, and a high purity Germanium detector for qualitative elemental analysis within photo-activation analysis method. 21 nuclei ranging from 24Na to 149Nd have been identified in the meteorite sample. (paper)

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.

SHARDA - a program for sample heat, activity, reactivity and dose analysis

International Nuclear Information System (INIS)

Shukla, V.K.; Bajpai, Anil

1985-01-01

A computer program SHARDA (Sample Heat, Activity, Reactivity and Dose Analysis) has been developed for safety evaluation of Pile Irradiation Request (PIR) for various nonfissile materials in the research reactor CIRUS. The code can also be used, with minor modifications, for PIR safety evaluations for the research reactor DHRUVA, now being commissioned. Most of the data needed for such analysis like isotopic abundances, their various nuclear cross-sections, gamma radiation and shielding data have been built in the code for all nonfissile naturally occuring elements. The PIR safety evaluations can be readily carried out using this code for any sample in elemental, compound or mixture form irradiated in any location of the reactor. This report describes the calculational model and the input/output details of the code. Some earlier irradiations carried out in CIRUS have been analysed using this code and the results have been compared with available operational measurements. (author)

Activation analysis. Chapter 4

International Nuclear Information System (INIS)

1976-01-01

The principle, sample and calibration standard preparation, activation by neutrons, charged particles and gamma radiation, sample transport after activation, activity measurement, and chemical sample processing are described for activation analysis. Possible applications are shown of nondestructive activation analysis. (J.P.)

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

Study of gamma ray analysis software's. Application to activation analysis of geological samples

International Nuclear Information System (INIS)

Silva, Luiz Roberto Nogueira da

1998-01-01

A comparative evaluation of the gamma-ray analysis software VISPECT, in relation to two commercial gamma-ray analysis software packages, OMNIGAM (EG and G Ortec) and SAMPO 90 (Canberra) was performed. For this evaluation, artificial gamma ray spectra were created, presenting peaks of different intensities and located at four different regions of the spectrum. Multiplet peaks with equal and different intensities, but with different channel separations, were also created. The results obtained showed a good performance of VISPECT in detecting and analysing single and multiplet peaks of different intensities in the gamma-ray spectrum. Neutron activation analysis of the geological reference material GS-N (IWG-GIT) and of the granite G-94, used in a Proficiency Testing Trial of Analytical Geochemistry Laboratories, was also performed , in order to evaluate the VISEPCT software in the analysis of real samples. The results obtained by using VISPECT were as good or better than the ones obtained using the other programs. (author)

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

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%

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.

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.

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

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.

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)

Derivative activation analysis of phosphorus at ppb levels in water samples

International Nuclear Information System (INIS)

Arunachalam, J.; John, A.; Gangadharan, S.

1991-01-01

A neutron activation analysis procedure has been developed for the indirect determination of phosphorus as orthophosphate at ppb levels, via the formation of antimonyl phosphomolybdic acid. The complex is adsorbed on Sephadex G-25 resin and the antimony is estimated through NAA, allowing the determination of phosphorus. The procedure provides an easy method to adopt for the routine determination of phosphorus at ≥ 10 ng ml -1 levels with good precision, in water samples. (author) 6 refs.; 5 tabs

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

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.

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.

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

Quantitative portable gamma-spectroscopy sample analysis for non-standard sample geometries

International Nuclear Information System (INIS)

Ebara, S.B.

1998-01-01

Utilizing a portable spectroscopy system, a quantitative method for analysis of samples containing a mixture of fission and activation products in nonstandard geometries was developed. This method was not developed to replace other methods such as Monte Carlo or Discrete Ordinates but rather to offer an alternative rapid solution. The method can be used with various sample and shielding configurations where analysis on a laboratory based gamma-spectroscopy system is impractical. The portable gamma-spectroscopy method involves calibration of the detector and modeling of the sample and shielding to identify and quantify the radionuclides present in the sample. The method utilizes the intrinsic efficiency of the detector and the unattenuated gamma fluence rate at the detector surface per unit activity from the sample to calculate the nuclide activity and Minimum Detectable Activity (MDA). For a complex geometry, a computer code written for shielding applications (MICROSHIELD) is utilized to determine the unattenuated gamma fluence rate per unit activity at the detector surface. Lastly, the method is only applicable to nuclides which emit gamma-rays and cannot be used for pure beta or alpha emitters. In addition, if sample self absorption and shielding is significant, the attenuation will result in high MDA's for nuclides which solely emit low energy gamma-rays. The following presents the analysis technique and presents verification results using actual experimental data, rather than comparisons to other approximations such as Monte Carlo techniques, to demonstrate the accuracy of the method given a known geometry and source term. (author)

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

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)

Prompt Gamma Activation Analysis (PGAA): Technique of choice for nondestructive bulk analysis of returned comet samples

International Nuclear Information System (INIS)

Lindstrom, D.J.; Lindstrom, R.M.

1989-01-01

Prompt gamma activation analysis (PGAA) is a well-developed analytical technique. The technique involves irradiation of samples in an external neutron beam from a nuclear reactor, with simultaneous counting of gamma rays produced in the sample by neutron capture. Capture of neutrons leads to excited nuclei which decay immediately with the emission of energetic gamma rays to the ground state. PGAA has several advantages over other techniques for the analysis of cometary materials: (1) It is nondestructive; (2) It can be used to determine abundances of a wide variety of elements, including most major and minor elements (Na, Mg, Al, Si, P, K, Ca, Ti, Cr, Mn, Fe, Co, Ni), volatiles (H, C, N, F, Cl, S), and some trace elements (those with high neutron capture cross sections, including B, Cd, Nd, Sm, and Gd); and (3) It is a true bulk analysis technique. Recent developments should improve the technique's sensitivity and accuracy considerably

Determination of mercury and copper in water samples by activation analysis using preconcentration on emission spectroscopic carbon powder

International Nuclear Information System (INIS)

Nagatsuka, Sumiko; Tanizaki, Yoshiyuki

1978-01-01

A simple preconcentration procedure for mercury and copper was examined in the activation analysis of water samples. The preconcentration using pure activated carbon has been reported in several papers. The authors found that the carbon powder for emission spectroscopic analysis showed the high purity equivalent to pure activated carbon. The influence of various parameters in adsorption conditions was studied by radioactive tracers 197 Hg and 64 Cu. It was confirmed that 100% of these elements were adsorbed on carbon powders as pyrrolidine dithiocarbonate complexes at an acidity of pH 6 - 8, the temperature of 50 0 C and the stirring time of 30 minutes. This method was applied to the activation analysis of the river water samples taken from the upper stream area of the Arakawa river and the ground water samples taken from the wells of the environs of Tokyo Megalopolis. The carbon powders which adsorbed these elements were filtered, dried and analyzed by instrumental neutron activation analysis. The Hg concentrations of 0.01 - 0.1 ppb in river water and 0.03 - 1.4 ppb in ground water were obtained as well as the Cu concentrations of 0.3 - 3.0 ppb in ground water. The limits of determination of this method are 0.01 ppb Hg and 0.2 ppb Cu in the case of 1.1 sample of fresh water. (auth.)

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)

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)

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)

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)

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

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)

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

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)

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.

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

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)

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.

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)

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

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

Field data analysis of active chlorine-containing stormwater samples.

Science.gov (United States)

Zhang, Qianyi; Gaafar, Mohamed; Yang, Rong-Cai; Ding, Chen; Davies, Evan G R; Bolton, James R; Liu, Yang

2018-01-15

Many municipalities in Canada and all over the world use chloramination for drinking water secondary disinfection to avoid DBPs formation from conventional chlorination. However, the long-lasting monochloramine (NH 2 Cl) disinfectant can pose a significant risk to aquatic life through its introduction into municipal storm sewer systems and thus fresh water sources by residential, commercial, and industrial water uses. To establish general total active chlorine (TAC) concentrations in discharges from storm sewers, the TAC concentration was measured in stormwater samples in Edmonton, Alberta, Canada, during the summers of 2015 and 2016 under both dry and wet weather conditions. The field-sampling results showed TAC concentration variations from 0.02 to 0.77 mg/L in summer 2015, which exceeds the discharge effluent limit of 0.02 mg/L. As compared to 2015, the TAC concentrations were significantly lower during the summer 2016 (0-0.24 mg/L), for which it is believed that the higher precipitation during summer 2016 reduced outdoor tap water uses. Since many other cities also use chloramines as disinfectants for drinking water disinfection, the TAC analysis from Edmonton may prove useful for other regions as well. Other physicochemical and biological characteristics of stormwater and storm sewer biofilm samples were also analyzed, and no significant difference was found during these two years. Higher density of AOB and NOB detected in the storm sewer biofilm of residential areas - as compared with other areas - generally correlated to high concentrations of ammonium and nitrite in this region in both of the two years, and they may have contributed to the TAC decay in the storm sewers. The NH 2 Cl decay laboratory experiments illustrate that dissolved organic carbon (DOC) concentration is the dominant factor in determining the NH 2 Cl decay rate in stormwater samples. The high DOC concentrations detected from a downstream industrial sampling location may contribute to a

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

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.

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

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.

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.

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

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)

Standardizing Activation Analysis: New Software for Photon Activation Analysis

Science.gov (United States)

Sun, Z. J.; Wells, D.; Segebade, C.; Green, J.

2011-06-01

Photon Activation Analysis (PAA) of environmental, archaeological and industrial samples requires extensive data analysis that is susceptible to error. For the purpose of saving time, manpower and minimizing error, a computer program was designed, built and implemented using SQL, Access 2007 and asp.net technology to automate this process. Based on the peak information of the spectrum and assisted by its PAA library, the program automatically identifies elements in the samples and calculates their concentrations and respective uncertainties. The software also could be operated in browser/server mode, which gives the possibility to use it anywhere the internet is accessible. By switching the nuclide library and the related formula behind, the new software can be easily expanded to neutron activation analysis (NAA), charged particle activation analysis (CPAA) or proton-induced X-ray emission (PIXE). Implementation of this would standardize the analysis of nuclear activation data. Results from this software were compared to standard PAA analysis with excellent agreement. With minimum input from the user, the software has proven to be fast, user-friendly and reliable.

Standardizing Activation Analysis: New Software for Photon Activation Analysis

International Nuclear Information System (INIS)

Sun, Z. J.; Wells, D.; Green, J.; Segebade, C.

2011-01-01

Photon Activation Analysis (PAA) of environmental, archaeological and industrial samples requires extensive data analysis that is susceptible to error. For the purpose of saving time, manpower and minimizing error, a computer program was designed, built and implemented using SQL, Access 2007 and asp.net technology to automate this process. Based on the peak information of the spectrum and assisted by its PAA library, the program automatically identifies elements in the samples and calculates their concentrations and respective uncertainties. The software also could be operated in browser/server mode, which gives the possibility to use it anywhere the internet is accessible. By switching the nuclide library and the related formula behind, the new software can be easily expanded to neutron activation analysis (NAA), charged particle activation analysis (CPAA) or proton-induced X-ray emission (PIXE). Implementation of this would standardize the analysis of nuclear activation data. Results from this software were compared to standard PAA analysis with excellent agreement. With minimum input from the user, the software has proven to be fast, user-friendly and reliable.

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)

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)

Evaluation of nuclear reactor based activation analysis techniques

International Nuclear Information System (INIS)

Obrusnik, I.; Kucera, J.

1977-09-01

A survey is presented of the basic types of activation analysis applied in environmental control. Reactor neutron activation analysis is described (including the reactor as a neutron source, sample activation in the reactor, methodology of neutron activation analysis, sample transport into the reactor and sample packaging after irradiation, instrumental activation analysis with radiochemical separation, data measurement and evaluation, sampling and sample preparation). Sources of environmental contamination with trace elements, sampling and sample analysis by neutron activation are described. The analysis is described of soils, waters and biological materials. Methods are shown of evaluating neutron activation analysis results and of their interpretation for purposes of environmental control. (J.B.)

Radiochemical analysis of phosphorus in milk samples

International Nuclear Information System (INIS)

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

1991-01-01

The determination of phosphorus in milk samples by thermal neutron activation analysis employing radiochemical separation is described. The radiochemical separation consists of the simultaneous irradiation of samples and standards, dissolution of the milk samples in a perchloric acid and nitric acid mixture, addition of zinc hold-back carrier, precipitation of phosphorus as ammonium phospho molybdate (A.M.P.) and sample counting in a Geiger-Mueller detector. The analysis sources of error were studied and the established method was applied to phosphorus analyses in commercial milk samples. (author)

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

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)

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)

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)

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

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)

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)

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)

BEAMGAA. A chance for high precision analysis of big samples

International Nuclear Information System (INIS)

Goerner, W.; Berger, A.; Haase, O.; Segebade, Chr.; Alber, D.; Monse, G.

2005-01-01

In activation analysis of traces in small samples, the non-equivalence of the activating radiation doses of sample and calibration material gives rise to sometimes tolerable systematic errors. Conversely, analysis of major components usually demands high trueness and precision. To meet this, beam geometry activation analysis (BEAMGAA) procedures have been developed for instrumental photon (IPAA) and neutron activation analysis (INAA) in which the activating neutron/photon beam exhibits broad, flat-topped characteristics. This results in a very low lateral activating flux gradient compared to known radiation facilities, however, at significantly lower flux density. The axial flux gradient can be accounted for by a monitor-sample-monitor assembly. As a first approach, major components were determined in high purity substances as well as selenium in a cattle fodder additive. (author)

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)

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)

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)

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

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)

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

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)

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)

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.)

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

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

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)

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

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)

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.)

Mercury and gold concentrations of highly polluted environmental samples determined using prompt gamma-ray analysis and instrument neutron activation analysis

Science.gov (United States)

Osawa, Takahito; Hatsukawa, Yuichi; Appel, Peter W. U.; Matsue, Hideaki

2011-04-01

The authors have established a method of determining mercury and gold in severely polluted environmental samples using prompt gamma-ray analysis (PGA) and instrumental neutron activation analysis (INAA). Since large amounts of mercury are constantly being released into the environment by small-scale gold mining in many developing countries, the mercury concentration in tailings and water has to be determined to mitigate environmental pollution. Cold-vapor atomic absorption analysis, the most pervasive method of mercury analysis, is not suitable because tailings and water around mining facilities have extremely high mercury concentrations. On the other hand, PGA can determine high mercury concentrations in polluted samples as it has an appropriate level of sensitivity. Moreover, gold concentrations can be determined sequentially by using INAA after PGA. In conclusion, the analytical procedure established in this work using PGA and INAA is the best way to evaluate the degree of pollution and the tailing resource value. This method will significantly contribute to mitigating problems in the global environment.

Mercury and gold concentrations of highly polluted environmental samples determined using prompt gamma-ray analysis and instrument neutron activation analysis

International Nuclear Information System (INIS)

Osawa, Takahito; Hatsukawa, Yuichi; Appel, Peter W.U.; Matsue, Hideaki

2011-01-01

The authors have established a method of determining mercury and gold in severely polluted environmental samples using prompt gamma-ray analysis (PGA) and instrumental neutron activation analysis (INAA). Since large amounts of mercury are constantly being released into the environment by small-scale gold mining in many developing countries, the mercury concentration in tailings and water has to be determined to mitigate environmental pollution. Cold-vapor atomic absorption analysis, the most pervasive method of mercury analysis, is not suitable because tailings and water around mining facilities have extremely high mercury concentrations. On the other hand, PGA can determine high mercury concentrations in polluted samples as it has an appropriate level of sensitivity. Moreover, gold concentrations can be determined sequentially by using INAA after PGA. In conclusion, the analytical procedure established in this work using PGA and INAA is the best way to evaluate the degree of pollution and the tailing resource value. This method will significantly contribute to mitigating problems in the global environment.

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.

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

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

Sampling and Analysis Plan for PUREX canyon vessel flushing

International Nuclear Information System (INIS)

Villalobos, C.N.

1995-01-01

A sampling and analysis plan is necessary to provide direction for the sampling and analytical activities determined by the data quality objectives. This document defines the sampling and analysis necessary to support the deactivation of the Plutonium-Uranium Extraction (PUREX) facility vessels that are regulated pursuant to Washington Administrative Code 173-303

UMTRA water sampling and analysis plan, Tuba City, Arizona

International Nuclear Information System (INIS)

1993-09-01

The purpose of this document is to provide background, guidance, and justification for fiscal year (FY) 1994 water sampling activities for the uranium mil tailings site at Tuba City, Arizona. This sampling and analysis plan will form the basis for groundwater sampling and analysis work orders to be implemented in FY94

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

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

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

Micropore-free surface-activated carbon for the analysis of polychlorinated dibenzo-p-dioxins-dibenzofurans and non-ortho-substituted polychlorinated biphenyls in environmental samples.

Science.gov (United States)

Kemmochi, Yukio; Tsutsumi, Kaori; Arikawa, Akihiro; Nakazawa, Hiroyuki

2002-11-22

2,3,7,8-Substituted polychlorinated dibenzo-p-dioxins/polychlorinated dibenzofurans (PCDD/Fs) and non-ortho-substituted polychlorinated biphenyls (PCBs) account for almost all of the total toxic equivalents (TEQ) in environmental samples. Activated carbon columns are used to fractionate the samples for GC-MS analysis or bioassay. Micropore-free surface-activated carbon is highly selective for PCDD/Fs and non-ortho-PCBs and can improve the conventional activated carbon column clean-up. Along with sulfuric acid-coated diatomaceous earth columns, micropore-free surface-activated carbon provides a rapid, robust, and high-throughput sample preparation method for PCDD/Fs and non-ortho-PCBs analysis.

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

Sampling and Analysis Plan for the 221-U Facility

International Nuclear Information System (INIS)

Rugg, J.E.

1998-02-01

This sampling and analysis plan (SAP) presents the rationale and strategy for the sampling and analysis activities proposed to be conducted to support the evaluation of alternatives for the final disposition of the 221-U Facility. This SAP will describe general sample locations and the minimum number of samples required. It will also identify the specific contaminants of potential concern (COPCs) and the required analysis. This SAP does not define the exact sample locations and equipment to be used in the field due to the nature of unknowns associated with the 221-U Facility

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.

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

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

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)

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

Sampling and sample preparation methods for the analysis of trace elements in biological material

International Nuclear Information System (INIS)

Sansoni, B.; Iyengar, V.

1978-05-01

The authors attempt to give a most systamtic possible treatment of the sample taking and sample preparation of biological material (particularly in human medicine) for trace analysis (e.g. neutron activation analysis, atomic absorption spectrometry). Contamination and loss problems are discussed as well as the manifold problems of the different consistency of solid and liquid biological materials, as well as the stabilization of the sample material. The process of dry and wet ashing is particularly dealt with, where new methods are also described. (RB) [de

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)

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

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

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

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

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.

Analytical laboratory quality assurance guidance in support of EM environmental sampling and analysis activities

International Nuclear Information System (INIS)

1994-05-01

This document introduces QA guidance pertaining to design and implementation of laboratory procedures and processes for collecting DOE Environmental Restoration and Waste Management (EM) ESAA (environmental sampling and analysis activities) data. It addresses several goals: identifying key laboratory issues and program elements to EM HQ and field office managers; providing non-prescriptive guidance; and introducing environmental data collection program elements for EM-263 assessment documents and programs. The guidance describes the implementation of laboratory QA elements within a functional QA program (development of the QA program and data quality objectives are not covered here)

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.

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.

Sampling and analysis plan for the preoperational environmental survey for the immobilized low activity waste (ILAW) project W-465

International Nuclear Information System (INIS)

Mitchell, R.M.

1998-01-01

This document provides a detailed description of the Sampling and Analysis Plan for the Preoperational Survey to be conducted at the Immobilized Low Activity Waste (ILAW) Project Site in the 200 East Area

Analysis of industrial coke samples by activation with cyclotron protons

International Nuclear Information System (INIS)

Chaudhri, M.A.; Lee, M.M.; Spicer, B.M.

1982-01-01

A Melbourne Petrochemical Company was experiencing excessive coke formation in its ''cracking furnaces'', which was causing unnecessary stoppage of production and wastage of energy due to additional insulation. In order to investigate the possible causes of this excessive coke formation, we analyzed various coke samples and other coke-like materials obtained from these furnaces by activation with cyclotron-protons. Our results showed that, out of the two suspected coke promoters As and Sb whose small concentration in feed would produce greatly accelerated coke formation, As could not be detected in any of the eight samples investigated, while Sb was present in only one sample. However, we did observe Ca, Cr and Fe in all the samples, with surprisingly high concentrations in some of them. It has, therefore, been suggested that Ca, and perhaps Cr and Fe, but not As or Sb, could have been responsible for the excessive coke formation in the ''cracking furnaces''

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.)

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)

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)

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

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.

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)

Impact of Cesium decontamination on performances of high activity sample analysis

Energy Technology Data Exchange (ETDEWEB)

Maillard, Christophe; Boyer-Deslys, Valerie; Dautheribes, Jean L.; Esbelin, Eric; Beres, Andre; Jan, Steve; Baghdadi, Sarah; Rivier, Cedric [CEA, Nuclear Energy Division, Bagnols sur Ceze (France). RadioChemistry and Processes Dept.

2017-09-01

Experiments in the ATALANTE facility can lead to high activity samples (for example the dissolution of hulls and spent fuels), essentially coming from the presence of {sup 137}Cs. Usually, these samples are handled in a shielded cell. The removal of this radionuclide from the sample would make it possible to handle it in glove boxes without having to perform an important dilution in the shielded cells beforehand. It would allow to analyze samples using techniques usually implemented in glove boxes (such as ICP, α spectrometry..) and to reach lower detection and quantification limits. To do so, a separation by extraction chromatography using a Triskem AMP-PAN column was developed. A cesium decontamination factor higher than 5 x 10{sup 4} and detection limits improvement up to a factor 100 were obtained.

UMTRA project water sampling and analysis plan, Maybell, Colorado

International Nuclear Information System (INIS)

1994-06-01

This water sampling and analysis plan (WSAP) describes planned water sampling activities and provides the regulatory and technical basis for ground water sampling in 1994 at the US Department of Energy's (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site in Maybell, Colorado. The WSAP identifies and justifies sampling locations, analytical parameters, and sampling frequencies at the site. The ground water data will be used for site characterization and risk assessment. The regulatory basis for the ground water and surface water monitoring activities is derived from the EPA regulations in 40 CFR Part 192 (1993) and the proposed EPA standards of 1987 (52 FR 36000). Sampling procedures are guided by the UMTRA Project standard operating procedures (SOP) (JEG, n.d.), the Technical Approach Document (TAD) (DOE, 1989), and the most effective technical approach for the site. This WSAP also includes a summary and the results of water sampling activities from 1989 through 1992 (no sampling was performed in 1993)

Quality assurance techniques for activation analysis

International Nuclear Information System (INIS)

Becker, D.A.

1984-01-01

The principles and techniques of quality assurance are applied to the measurement method of activation analysis. Quality assurance is defined to include quality control and quality assessment. Plans for quality assurance include consideration of: personnel; facilities; analytical design; sampling and sample preparation; the measurement process; standards; and documentation. Activation analysis concerns include: irradiation; chemical separation; counting/detection; data collection, and analysis; and calibration. Types of standards discussed include calibration materials and quality assessment materials

Classification of Surface and Deep Soil Samples Using Linear Discriminant Analysis

International Nuclear Information System (INIS)

Wasim, M.; Ali, M.; Daud, M.

2015-01-01

A statistical analysis was made of the activity concentrations measured in surface and deep soil samples for natural and anthropogenic gamma-emitting radionuclides. Soil samples were obtained from 48 different locations in Gilgit, Pakistan covering about 50 km/sup 2/ areas at an average altitude of 1550 m above sea level. From each location two samples were collected: one from the top soil (2-6 cm) and another from a depth of 6-10 cm. Four radionuclides including /sup 226/Ra, /sup 232/Th, /sup 40/K and /sup 137/Cs were quantified. The data was analyzed using t-test to find out activity concentration difference between the surface and depth samples. At the surface, the median activity concentrations were 23.7, 29.1, 4.6 and 115 Bq kg/sup -1/ for 226Ra, 232Th, 137Cs and 40K respectively. For the same radionuclides, the activity concentrations were respectively 25.5, 26.2, 2.9 and 191 Bq kg/sup -1/ for the depth samples. Principal component analysis (PCA) was applied to explore patterns within the data. A positive significant correlation was observed between the radionuclides /sup 226/Ra and /sup 232/Th. The data from PCA was further utilized in linear discriminant analysis (LDA) for the classification of surface and depth samples. LDA classified surface and depth samples with good predictability. (author)

Automated activation-analysis system

International Nuclear Information System (INIS)

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

1982-01-01

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

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)

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)

Sampling and Analysis Instruction for the 384 Day Tank

International Nuclear Information System (INIS)

Smith, D. S.

1999-01-01

This instruction defines the sampling and analysis activities to be performed in support of the decommissioning of the 384 Day Tanks. The purpose of the sampling is to determine whether a release from the tanks has occurred and the extent of the contamination, if any

Sampling and Analysis Plan for the 216-A-29 Ditch

International Nuclear Information System (INIS)

Petersen, S.W.

1998-06-01

This sampling and analysis plan defines procedures to be used for collecting and handling samples to be obtained from the 216-A-29 Ditch, and identifies requirements for field and laboratory measurements. The sampling strategy describes here is derived from a Data Quality Objectives workshop conducted in January 1997 to support sampling to assure worker safety during construction and to assess the validity of a 1988 ditch sampling campaign and the effectiveness of subsequent stabilization. The purpose of the proposed sampling and analysis activities is to characterize soil contamination in the vicinity of a proposed road over the 216-A-29 Ditch

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

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

Integrated sampling and analysis plan for samples measuring >10 mrem/hour

International Nuclear Information System (INIS)

Haller, C.S.

1992-03-01

This integrated sampling and analysis plan was prepared to assist in planning and scheduling of Hanford Site sampling and analytical activities for all waste characterization samples that measure greater than 10 mrem/hour. This report also satisfies the requirements of the renegotiated Interim Milestone M-10-05 of the Hanford Federal Facility Agreement and Consent Order (the Tri-Party Agreement). For purposes of comparing the various analytical needs with the Hanford Site laboratory capabilities, the analytical requirements of the various programs were normalized by converting required laboratory effort for each type of sample to a common unit of work, the standard analytical equivalency unit (AEU). The AEU approximates the amount of laboratory resources required to perform an extensive suite of analyses on five core segments individually plus one additional suite of analyses on a composite sample derived from a mixture of the five core segments and prepare a validated RCRA-type data package

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.

Guidance for establishment and implementation of a national sample management program in support of EM environmental sampling and analysis activities

International Nuclear Information System (INIS)

1994-01-01

The role of the National Sample Management Program (NSMP) proposed by the Department of Energy's Office of Environmental Management (EM) is to be a resource for EM programs and for local Field Sample Management Programs (FSMPs). It will be a source of information on sample analysis and data collection within the DOE complex. Therefore the NSMP's primary role is to coordinate and function as a central repository for information collected from the FSMPs. An additional role of the NSMP is to monitor trends in data collected from the FSMPs over time and across sites and laboratories. Tracking these trends will allow identification of potential problems in the sampling and analysis process

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

Activation analysis of air particulate matter

International Nuclear Information System (INIS)

Alian, A.; Sansoni, B.

1988-11-01

This review on activation analysis of air particulate matter is an extended and updated version of a review given by the same authors in 1985. The main part is aimed at the analytical scheme and refers to rules and techniques for sampling, sample and standard preparation, irradiation and counting procedures, as well as data processing, - evaluation, and - presentation. Additional chapters deal with relative and monostandard methods, the use of activation analysis for atmosphere samples in various localities, and level of toxic and other elements in the atmosphere. The review contains 190 references. (RB)

Method Comparison of Neutron Activation Analysis and Atomic Absorption Spectrometry for Determination of Zinc in Food Samples

International Nuclear Information System (INIS)

Endah Damastuti; Syukria Kurniawati; Natalia Adventini

2009-01-01

Zinc as a micro nutrient, has important roles in human metabolism system. It is required by the body in appropriate amount from food intake. Due to the very low concentration of Zinc in food, high selectivity and sensitivity analysis technique is required for the determination, such as Neutron Activation Analysis (NAA) and Atomic Absorption Spectrometry (AAS). In this experiment, both methods were compared in zinc analysis of food samples. The subject of this experiment is to examine of those methods conformity and improving the technique capability in zinc analysis in food sample. Those methods were validated by analyzing zinc in SRM NIST 1548a Typical Diet and were tested its accuracy and precision. The results of Zn concentration were 25.1 ± 2.14 mg/kg by NAA and 24.1 ± 1.40 mg/kg by AAS while the certificate value was 24.6 ± 1.80 mg/kg. Percentage of relative bias, %CV, μ-test score and HORRAT(Horwitz ratio) value given by NAA were 2%, 8.5%, 0.18 and 0.9 respectively, while %relative bias, %CV, μ-test score and HORRAT value given by AAS were 2%, 5.8 %, 0.20 and 0.6 respectively. The result obtained for Zn concentration in various food samples by NAA and AAS were varied from 13.7 – 29.3 mg/kg with mean value 19.8 mg/kg and 11.2 – 26.0 mg/kg with mean value 17.3 mg/kg (author)

Analysis of mercury and selenium in biological samples by neutron activation analysis

International Nuclear Information System (INIS)

Catharino, Marilia Gabriela Miranda

2002-01-01

In the present work, hair samples from populations suspected of contamination by mercury, in the localities of Serra do Navio, Vila Nova and Tartarugalzinho, in the State of Amapa, were analyzed. Hair samples of children under odontopediatric treatment were also analyzed for mercury, in order to study the possibility of transfer of mercury from the dental amalgam and also to obtain data of hair mercury in a control population of children. Another step of the work was the development of a method for the determination of selenium, by using the short-lived radioisotope 77 mSe. After the certification of the method it was applied to the analysis of hair, nails and a vitamin supplement. A comparison was made with the results obtain ed by using the long-lived radioisotope of selenium, 75 Se. The results obtained for mercury in the hair samples of populations living in the State of Amapa have shown that the mercury concentrations in these populations are much higher than in the controls. As for the hair samples of children under treatment with mercury amalgam, no significant differences were found in the concentrations of mercury after the treatment. On the other hand, these data were important to obtain data for a control population of children. The results obtained by using the radioisotope 77 mSe showed that the method developed was suitable for the analyzed matrixes and the results were similar to the ones obtained by employing the usual AANI method, with the radioisotope 75 Se. (author)

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)

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

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)

Analysis of Precision of Activation Analysis Method

DEFF Research Database (Denmark)

Heydorn, Kaj; Nørgaard, K.

1973-01-01

The precision of an activation-analysis method prescribes the estimation of the precision of a single analytical result. The adequacy of these estimates to account for the observed variation between duplicate results from the analysis of different samples and materials, is tested by the statistic T...

Application of WSP method in analysis of environmental samples

International Nuclear Information System (INIS)

Stacho, M.; Slugen, V.; Hinca, R.; Sojak, S.; Krnac, S.

2014-01-01

Detection of activity in natural samples is specific especially because of its low level and high background interferences. Reduction of background interferences could be reached using low background chamber. Measurement geometry in shape of Marinelli beaker is commonly used according to low level of activity in natural samples. The Peak Net Area (PNA) method is the world-wide accepted technique for analysis of gamma-ray spectra. It is based on the net area calculation of the full energy peak, therefore, it takes into account only a fraction of measured gamma-ray spectrum. On the other hand, the Whole Spectrum Processing (WSP) approach to the gamma analysis makes possible to use entire information being in the spectrum. This significantly raises efficiency and improves energy resolution of the analysis. A principal step for the WSP application is building up the suitable response operator. Problems are put in an appearance when suitable standard calibration sources are unavailable. It may be occurred in the case of large volume samples and/or in the analysis of high energy range. Combined experimental and mathematical calibration may be a suitable solution. Many different detectors have been used to register the gamma ray and its energy. HPGe detectors produce the highest resolution commonly available today. Therefore they are they the most often used detectors in natural samples activity analysis. Scintillation detectors analysed using PNA method could be also used in simple cases, but for complicated spectra are practically inapplicable. WSP approach improves resolution of scintillation detectors and expands their applicability. WSP method allowed significant improvement of the energetic resolution and separation of "1"3"7Cs 661 keV peak from "2"1"4Bi 609 keV peak. At the other hand the statistical fluctuations in the lower part of the spectrum highlighted by background subtraction causes that this part is still not reliably analyzable. (authors)

Seasonal Variation, Chemical Composition and Antioxidant Activity of Brazilian Propolis Samples

Directory of Open Access Journals (Sweden)

Érica Weinstein Teixeira

2010-01-01

Full Text Available Total phenolic contents, antioxidant activity and chemical composition of propolis samples from three localities of Minas Gerais state (southeast Brazil were determined. Total phenolic contents were determined by the Folin–Ciocalteau method, antioxidant activity was evaluated by DPPH, using BHT as reference, and chemical composition was analyzed by GC/MS. Propolis from Itapecerica and Paula Cândido municipalities were found to have high phenolic contents and pronounced antioxidant activity. From these extracts, 40 substances were identified, among them were simple phenylpropanoids, prenylated phenylpropanoids, sesqui- and diterpenoids. Quantitatively, the main constituent of both samples was allyl-3-prenylcinnamic acid. A sample from Virginópolis municipality had no detectable phenolic substances and contained mainly triterpenoids, the main constituents being α- and β-amyrins. Methanolic extracts from Itapecerica and Paula Cândido exhibited pronounced scavenging activity towards DPPH, indistinguishable from BHT activity. However, extracts from Virginópolis sample exhibited no antioxidant activity. Total phenolic substances, GC/MS analyses and antioxidant activity of samples from Itapecerica collected monthly over a period of 1 year revealed considerable variation. No correlation was observed between antioxidant activity and either total phenolic contents or contents of artepillin C and other phenolic substances, as assayed by CG/MS analysis.

Sampling and Analysis Plan for the 233-S Plutonium Concentration Facility

International Nuclear Information System (INIS)

Mihalic, M.A.

1998-02-01

This Sampling and Analysis Plan (SAP) provides the information and instructions to be used for sampling and analysis activities in the 233-S Plutonium Concentration Facility. The information and instructions herein are separated into three parts and address the Data Quality Objective (DQO) Summary Report, Quality Assurance Project Plan (QAP), and SAP

PIXE analysis of thin samples

International Nuclear Information System (INIS)

Kiss, Ildiko; Koltay, Ede; Szabo, Gyula; Laszlo, S.; Meszaros, A.

1985-01-01

Particle-induced X-ray emission (PIXE) multielemental analysis of thin film samples are reported. Calibration methods of K and L X-lines are discussed. Application of PIXE analysis to aerosol monitoring, multielement aerosol analysis is described. Results of PIXE analysis of samples from two locations in Hungary are compared with the results of aerosol samples from Scandinavia and the USA. (D.Gy.)

Activation analysis in Greece

International Nuclear Information System (INIS)

Grimanis, A.P.

1985-01-01

A review of research and development on NAA as well as examples of applications of this method are presented, taken from work carried out over the last 21 years at the Radioanalytical Laboratory of the Department of Chemistry in the Greek Nuclear Research Center ''Demokritos''. Improved and faster radiochemical NAA methods have been developed for the determination of Au, Ni, Cl, As, Cu, U, Cr, Eu, Hg and Mo in several materials, for the simultaneous determination of Br and I; Mg, Sr and Ni; As and Cu; As, Sb and Hg; Mn, Sr and Ba; Cd and Zn; Se and As; Mo and Cr in biological materials. Instrumental NAA methods have also been developed for the determination of Ag, Cl and Na in lake waters, Al, Ca, Mg and V in wines, 7 trace elements in biological materials, 17 trace elements in sediments and 20 minor and trace elements in ceramics. A comprehensive computer program for routine activation analysis using Ge(Li) detectors have been worked out. A rather extended charged-particle activation analysis program is carried out for the last 10 years, including particle induced X-ray emission (PIXE) analysis, particle induced prompt gamma-ray emission analysis (PIGE), other nuclear reactions and proton activation analysis. A special neutron activation method, the delayed fission neutron counting method is used for the analysis of fissionable elements, as U, Th, Pu, in samples of the whole nuclear fuel cycle including geological, enriched and nuclear safeguards samples

Sampling and sample processing in pesticide residue analysis.

Science.gov (United States)

Lehotay, Steven J; Cook, Jo Marie

2015-05-13

Proper sampling and sample processing in pesticide residue analysis of food and soil have always been essential to obtain accurate results, but the subject is becoming a greater concern as approximately 100 mg test portions are being analyzed with automated high-throughput analytical methods by agrochemical industry and contract laboratories. As global food trade and the importance of monitoring increase, the food industry and regulatory laboratories are also considering miniaturized high-throughput methods. In conjunction with a summary of the symposium "Residues in Food and Feed - Going from Macro to Micro: The Future of Sample Processing in Residue Analytical Methods" held at the 13th IUPAC International Congress of Pesticide Chemistry, this is an opportune time to review sampling theory and sample processing for pesticide residue analysis. If collected samples and test portions do not adequately represent the actual lot from which they came and provide meaningful results, then all costs, time, and efforts involved in implementing programs using sophisticated analytical instruments and techniques are wasted and can actually yield misleading results. This paper is designed to briefly review the often-neglected but crucial topic of sample collection and processing and put the issue into perspective for the future of pesticide residue analysis. It also emphasizes that analysts should demonstrate the validity of their sample processing approaches for the analytes/matrices of interest and encourages further studies on sampling and sample mass reduction to produce a test portion.

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)

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.

Automated activation-analysis system

International Nuclear Information System (INIS)

Minor, M.M.; Hensley, W.K.; Denton, M.M.; Garcia, S.R.

1981-01-01

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. The system and its mode of operation for a large reconnaissance survey are described

UMTRA Project water sampling and analysis plan, Gunnison, Colorado: Revision 1

International Nuclear Information System (INIS)

1994-11-01

This water sampling and analysis plan summarizes the results of previous water sampling activities and the plan for future water sampling activities, in accordance with the Guidance Document for Preparing Sampling and Analysis Plans for UMTRA Sites. A buffer zone monitoring plan for the Dos Rios Subdivision is included as an appendix. The buffer zone monitoring plan was developed to ensure continued protection to the public from residual contamination. The buffer zone is beyond the area depicted as contaminated ground water due to former milling operations. Surface remedial action at the Gunnison Uranium Mill Tailings Remedial Action Project site began in 1992; completion is expected in 1995. Ground water and surface water will be sampled semiannually at the Gunnison processing site and disposal site. Results of previous water sampling at the Gunnison processing site indicate that ground water in the alluvium is contaminated by the former uranium processing activities. Background ground water conditions have been established in the uppermost aquifer at the Gunnison disposal site. The monitor well locations provide a representative distribution of sampling points to characterize ground water quality and ground water flow conditions in the vicinity of the sites. The list of analytes has been modified with time to reflect constituents that are related to uranium processing activities and the parameters needed for geochemical evaluation

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

Activation analysis in national economy

International Nuclear Information System (INIS)

1974-01-01

The collected papers are based on the materials of the III All-Union Activation Analysis Meeting. The papers selected deal with the theoretical questions of the activation analysis, its hardware, latest developments in the field of automatic analysis and computer methods employment in the treatment of analytical information. Described are the new techniques for determination of a large number of elements in samples of biological and geological origin. Some results of the use of the activation analysis in various fields of science and technology are provided. The volume reflects the present status of activation analysis techniques in the USSR and might be of interest both for specialists, and for those involved in obtaining and using information on the composition of substances. (auth.)

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

UMTRA project water sampling and analysis plan, Gunnison, Colorado

International Nuclear Information System (INIS)

1994-06-01

This water sampling and analysis plan summarizes the results of previous water sampling activities and the plan for water sampling activities for calendar year 1994. A buffer zone monitoring plan is included as an appendix. The buffer zone monitoring plan is designed to protect the public from residual contamination that entered the ground water as a result of former milling operations. Surface remedial action at the Gunnison Uranium Mill Tailings Remedial Action Project site began in 1992; completion is expected in 1995. Ground water and surface water will be sampled semiannually in 1994 at the Gunnison processing site (GUN-01) and disposal site (GUN-08). Results of previous water sampling at the Gunnison processing site indicate that ground water in the alluvium is contaminated by the former uranium processing activities. Background ground water conditions have been established in the uppermost aquifer (Tertiary gravels) at the Gunnison disposal site. The monitor well locations provide a representative distribution of sampling points to characterize ground water quality and ground water flow conditions in the vicinity of the sites. The list of analytes has been modified with time to reflect constituents that are related to uranium processing activities and the parameters needed for geochemical evaluation. Water sampling will be conducted at least semiannually during and one year following the period of construction activities, to comply with the ground water protection strategy discussed in the remedial action plan (DOE, 1992a)

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

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

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

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

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.)

Judgment on the presence of radionuclides in sample analysis: A case study

International Nuclear Information System (INIS)

Muhamat Omar; Zalina Laili; Mohd Suhaimi Hamzah

2012-01-01

Qualitative and quantitative analysis of samples require good judgment from the analysts. These two aspects in gamma spectrometric analysis of Proficiency Test and solid radioactive waste samples for the determination of radionuclides are discussed. It is vital to judge and decide what energy peaks belong to which radionuclides prior to the creation of customized radionuclide library for the analysis of specific samples. Corrections due to radionuclide decay and growth, and the half-life assigned to a particular radionuclide in the uranium and thorium series are also discussed. Discussion on judgment to confirm the presence of thorium in food samples based on gamma spectrometry and neutron activation analysis is also provided. (author)

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

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).

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)

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

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)

Sampling and analysis methods for geothermal fluids and gases

Energy Technology Data Exchange (ETDEWEB)

Watson, J.C.

1978-07-01

The sampling procedures for geothermal fluids and gases include: sampling hot springs, fumaroles, etc.; sampling condensed brine and entrained gases; sampling steam-lines; low pressure separator systems; high pressure separator systems; two-phase sampling; downhole samplers; and miscellaneous methods. The recommended analytical methods compiled here cover physical properties, dissolved solids, and dissolved and entrained gases. The sequences of methods listed for each parameter are: wet chemical, gravimetric, colorimetric, electrode, atomic absorption, flame emission, x-ray fluorescence, inductively coupled plasma-atomic emission spectroscopy, ion exchange chromatography, spark source mass spectrometry, neutron activation analysis, and emission spectrometry. Material on correction of brine component concentrations for steam loss during flashing is presented. (MHR)

Gamma spectroscopy analysis of archived Marshall Island soil samples

International Nuclear Information System (INIS)

Herman, S.; Hoffman, K.; Lavelle, K.; Trauth, A.; Glover, S.E.; Connick, W.; Spitz, H.; LaMont, S.P.; Hamilton, T.

2016-01-01

Four samples of archival Marshall Islands soil were subjected to non-destructive, broad energy (17 keV-2.61 MeV) gamma-ray spectrometry analysis using a series of different high-resolution germanium detectors. These archival samples were collected in 1967 from different locations on Bikini Atoll and were contaminated with a range of fission and activation products, and other nuclear material from multiple weapons tests. Unlike samples collected recently, these samples have been stored in sealed containers and have been unaffected by approximately 50 years of weathering. Initial results show that the samples contained measurable but proportionally different concentrations of plutonium, 241 Am, and 137 Cs, and 60 Co. (author)

Sampling and chemical analysis in environmental samples around Nuclear Power Plants and some environmental samples

Energy Technology Data Exchange (ETDEWEB)

Cho, Yong Woo; Han, Man Jung; Cho, Seong Won; Cho, Hong Jun; Oh, Hyeon Kyun; Lee, Jeong Min; Chang, Jae Sook [KORTIC, Taejon (Korea, Republic of)

2002-12-15

Twelve kinds of environmental samples such as soil, seawater, underground water, etc. around Nuclear Power Plants(NPPs) were collected. Tritium chemical analysis was tried for the samples of rain water, pine-needle, air, seawater, underground water, chinese cabbage, a grain of rice and milk sampled around NPPs, and surface seawater and rain water sampled over the country. Strontium in the soil that sere sampled at 60 point of district in Korea were analyzed. Tritium were sampled at 60 point of district in Korea were analyzed. Tritium were analyzed in 21 samples of surface seawater around the Korea peninsular that were supplied from KFRDI(National Fisheries Research and Development Institute). Sampling and chemical analysis environmental samples around Kori, Woolsung, Youngkwang, Wooljin Npps and Taeduk science town for tritium and strontium analysis was managed according to plans. Succeed to KINS after all samples were tried.

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)

Gamma self-shielding correction factors calculation for aqueous bulk sample analysis by PGNAA technique

International Nuclear Information System (INIS)

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

2009-01-01

In this paper bulk sample prompt gamma neutron activation analysis (BSPGNAA) was applied to aqueous sample analysis using a relative method. For elemental analysis of an unknown bulk sample, gamma self-shielding coefficient was required. Gamma self-shielding coefficient of unknown samples was estimated by an experimental method and also by MCNP code calculation. The proposed methodology can be used for the determination of the elemental concentration of unknown aqueous samples by BSPGNAA where knowledge of the gamma self-shielding within the sample volume is required.

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

Sampling and Analysis Instruction for the 120-F-1 Glass Dump Site

International Nuclear Information System (INIS)

Brown, T.M.

1998-01-01

This sampling and analysis instruction has been prepared to clearly define the sampling and analysis activities to be performed to develop the basis for surveillance and maintenance of the 120-F-1 Glass Dumpsite. The purpose of this investigation is to augment historical information and obtain data to establish a technical basis for surveillance and maintenance at the site

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)

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.

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)

A simple method of correcting for variation of sample thickness in the determination of the activity of environmental samples by gamma spectrometry

International Nuclear Information System (INIS)

Galloway, R.B.

1991-01-01

Gamma ray spectrometry is a well established method of determining the activity of radioactive components in environmental samples. It is usual to maintain precisely the same counting geometry in measurements on samples under investigation as in the calibration measurements on standard materials of known activity, thus avoiding perceived uncertainties and complications in correcting for changes in counting geometry. However this may not always be convenient if, as on some occasions, only a small quantity of sample material is available for analysis. A procedure which avoids re-calibration for each sample size is described and is shown to be simple to use without significantly reducing the accuracy of measurement of the activity of typical environmental samples. The correction procedure relates to the use of cylindrical samples at a constant distance from the detector, the samples all having the same diameter but various thicknesses being permissible. (author)

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

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

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)

Analysis of monazite samples

International Nuclear Information System (INIS)

Kartiwa Sumadi; Yayah Rohayati

1996-01-01

The 'monazit' analytical program has been set up for routine work of Rare Earth Elements analysis in the monazite and xenotime minerals samples. Total relative error of the analysis is very low, less than 2.50%, and the reproducibility of counting statistic and stability of the instrument were very excellent. The precision and accuracy of the analytical program are very good with the maximum percentage relative are 5.22% and 1.61%, respectively. The mineral compositions of the 30 monazite samples have been also calculated using their chemical constituents, and the results were compared to the grain counting microscopic analysis

Analysis of submicrogram samples by INAA

Energy Technology Data Exchange (ETDEWEB)

Lindstrom, D J [National Aeronautics and Space Administration, Houston, TX (USA). Lyndon B. Johnson Space Center

1990-12-20

Procedure have been developed to increase the sensitivity of instrumental neutron activation analysis (INAA) so that cosmic-dust samples weighing only 10{sup -9}-10{sup -7} g are routinely analyzed for a sizable number of elements. The primary differences from standard techniques are: (1) irradiation of the samples is much more intense, (2) gamma ray assay of the samples is done using long counting times and large Ge detectors that are operated in an excellent low-background facility, (3) specially prepared glass standards are used, (4) samples are too small to be weighed routinely and concentrations must be obtained indirectly, (5) sample handling is much more difficult, and contamination of small samples with normally insignificant amounts of contaminants is difficult to prevent. In spite of the difficulties, INAA analyses have been done on 15 cosmic-dust particles and a large number of other stratospheric particles. Two-sigma detection limits for some elements are in the range of femtograms (10{sup -15} g), e.g. Co=11, Sc=0.9, Sm=0.2 A particle weighing just 0.2 ng was analyzed, obtaining abundances with relative analytical uncertainties of less than 10% for four elements (Fe, Co, Ni and Sc), which were sufficient to allow identification of the particle as chondritic interplanetary dust. Larger samples allow abundances of twenty or more elements to be obtained. (orig.).

Studies on cellular distribution of elements in human hepatocellular carcinoma samples by molecular activation analysis

International Nuclear Information System (INIS)

Deng Guilong; Chen Chunying; Zhang Peiqun; Zhao Jiujiang; Chai Zhifang

2005-01-01

The distribution patterns of 17 elements in the subcellular fractions of nuclei, mitochondria, lysosome, microsome and cytosol of human hepatocellular carcinoma (HCC) and normal liver samples were investigated by using molecular activation analysis (MAA) and differential centrifugation. Their significant difference was checked by the Studient's t-test. These elements exhibit inhomogeneous distributions in each subcellular fraction. Some elements have no significant difference between hepatocellular carcinoma and normal liver samples. However, the concentrations of Br, Ca, Cd and Cs are significantly higher in each component of hepatocarcinoma than in normal liver. The content of Fe in microsome of HCC is significantly lower, almost half of normal liver samples, but higher in other subcellular fractions than in those of normal tissues. The rare earth elements of La and Ce have the patterns similar to Fe. The concentrations of Sb and Zn in nuclei of HCC are obviously lower (P<0.05, P<0.05). The contents of K and Na are higher in cytosol of HCC (P<0.05). The distributions of Ba and Rb show no significant difference between two groups. The relationships of Fe, Cd and K with HCC were also discussed. The levels of some elements in subcellular fractions of tumor were quite different from those of normal liver, which suggested that trace elements might play important roles in the occurrence and development of hepatocellular carcinoma. (authors)

Studies on cellular distribution of elements in human hepatocellular carcinoma samples by molecular activation analysis

Energy Technology Data Exchange (ETDEWEB)

Guilong, Deng [Chinese Academy of Sciences, Beijing (China). Inst. of High Energy Physics, Key Laboratory of Nuclear Analytical Techniques; Department of General Surgery, the Second Affiliated Hospital, School of Medicine, Zhejiang Univ., Hangzhou (China); Chunying, Chen; Peiqun, Zhang; Jiujiang, Zhao; Zhifang, Chai [Chinese Academy of Sciences, Beijing (China). Inst. of High Energy Physics, Key Laboratory of Nuclear Analytical Techniques; Yingbin, Liu; Jianwei, Wang; Bin, Xu; Shuyou, Peng [Department of General Surgery, the Second Affiliated Hospital, School of Medicine, Zhejiang Univ., Hangzhou (China)

2005-07-15

The distribution patterns of 17 elements in the subcellular fractions of nuclei, mitochondria, lysosome, microsome and cytosol of human hepatocellular carcinoma (HCC) and normal liver samples were investigated by using molecular activation analysis (MAA) and differential centrifugation. Their significant difference was checked by the Studient's t-test. These elements exhibit inhomogeneous distributions in each subcellular fraction. Some elements have no significant difference between hepatocellular carcinoma and normal liver samples. However, the concentrations of Br, Ca, Cd and Cs are significantly higher in each component of hepatocarcinoma than in normal liver. The content of Fe in microsome of HCC is significantly lower, almost half of normal liver samples, but higher in other subcellular fractions than in those of normal tissues. The rare earth elements of La and Ce have the patterns similar to Fe. The concentrations of Sb and Zn in nuclei of HCC are obviously lower (P<0.05, P<0.05). The contents of K and Na are higher in cytosol of HCC (P<0.05). The distributions of Ba and Rb show no significant difference between two groups. The relationships of Fe, Cd and K with HCC were also discussed. The levels of some elements in subcellular fractions of tumor were quite different from those of normal liver, which suggested that trace elements might play important roles in the occurrence and development of hepatocellular carcinoma. (authors)

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)

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

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

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

Compatibility Grab Sampling and Analysis Plan for FY 2000

International Nuclear Information System (INIS)

SASAKI, L.M.

1999-01-01

This sampling and analysis plan (SAP) identifies characterization objectives pertaining to sample collection, laboratory analytical evaluation, and reporting requirements for grab samples obtained to address waste compatibility. It is written in accordance with requirements identified in Data Quality Objectives for Tank Farms Waste Compatibility Program (Mulkey et al. 1999) and Tank Farm Waste Transfer Compatibility Program (Fowler 1999). In addition to analyses to support Compatibility, the Waste Feed Delivery program has requested that tank samples obtained for Compatibility also be analyzed to confirm the high-level waste and/or low-activity waste envelope(s) for the tank waste (Baldwin 1999). The analytical requirements to confirm waste envelopes are identified in Data Quality Objectives for TWRS Privatization Phase I: Confirm Tank T is an Appropriate Feed Source for Low-Activity Waste Feed Batch X (Nguyen 1999a) and Data Quality Objectives for RPP Privatization Phase I: Confirm Tank T is an Appropriate Feed Source for High-Level Waste Feed Batch X (Nguyen 1999b)

Sampling and analysis plan for remediation of Operable Unit 100-IU-3 waste site 600-104

International Nuclear Information System (INIS)

1997-08-01

This sampling and analysis plan (SAP) presents the rationale and strategy for the sampling and analysis activities to support remediation of 100-IU-3 Operable Unit waste site 600-104. The purpose of the proposed sampling and analysis activities is to demonstrate that time-critical remediation of the waste site for soil containing 2,4-Dichlorophonoxyacetic acid salts and esters (2,4-D) and dioxin/furan isomers at concentrations that exceed cleanup levels has been effective. This shall be accomplished by sampling various locations of the waste site before and after remediation, analyzing the samples, and comparing the results to action levels set by the Washington State Department of Ecology

Utilization of chemical derivatives in activation analysis

International Nuclear Information System (INIS)

Ehmann, W.D.

1990-01-01

Derivative activation analysis (DAA) is a method to enhance the sensitivity of nuclear activation analysis for the more elusive elements. It may also allow a degree of chemical speciation for the element of interest. DAA uses a preirradiation chemical reaction on the sample to initiate the formation of, or an exchange with, a chemical complex which contains a surrogate element, M. As a result, the amount of the element or the chemical species to be determined, X, is now represented by measurement of the amount of the surrogate element, M, that is made part of, or released by the complex species. The surrogate element is selected for its superior properties for nuclear activation analysis and the absence of interference reaction in its final determination by instrumental neutron activation analysis (INAA) after some preconcentration or separation chemistry. Published DAA studies have been limited to neutron activation analysis. DAA can offer the analyst some important advantages. It can determine elements, functional groups, or chemical species which cannot be determined directly by INAA, fast neutron activation analysis (FNAA), prompt gamma neutron activation analysis (PGNAA), or charged particle activation analysis (CPAA) procedures. When compared with conventional RNAA, there are fewer precautions with respect to handling of intensely radioactive samples, since the chemistry is done before the irradiation. The preirradiation chemistry may also eliminate many interferences that might occur in INAA and, through use of an appropriate surrogate element, can place the analytical gamma-ray line in an interference-free region of the gamma-ray spectrum

The use of physical methods for elemental analysis of ecological samples

International Nuclear Information System (INIS)

Kudryashov, V.I.; Zhuravleva, E.L.; Maslov, O.D.

1996-01-01

The possibility of the application of difference X-ray and instrumental activation methods elemental analysis of rock ice, snow, water, soil and other natural samples was investigated. The content of some elements in ice samples from the glaciers of the Pamirs-Alaj mountain system for period 1973-1984 years has been determined. The recommendations for the choice of analysis methods with the aim of the environmental control have been given. (author). 10 refs., 6 figs., 1 tab

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)

UMTRA Project water sampling and analysis plan, Grand Junction, Colorado. Revision 1, Version 6

International Nuclear Information System (INIS)

1995-09-01

This water sampling and analysis plan describes the planned, routine ground water sampling activities at the Grand Junction US DOE Uranium Mill Tailings Remedial Action (UMTRA) Project site (GRJ-01) in Grand Junction, Colorado, and at the Cheney Disposal Site (GRJ-03) near Grand Junction. The plan identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequencies for the routine monitoring stations at the sites. Regulatory basis is in the US EPA regulations in 40 CFR Part 192 (1994) and EPA ground water quality standards of 1995 (60 FR 2854). This plan summarizes results of past water sampling activities, details water sampling activities planned for the next 2 years, and projects sampling activities for the next 5 years

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

Improving Sampling, Analysis, and Data Management for Site Investigation and Cleanup

Science.gov (United States)

The United States Environmental Protection Agency (EPA) supports the adoption of streamlined approaches to sampling, analysis, and data management activities conducted during site assessment, characterization, and cleanup.

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

The Chemical Characterization of Nigerian Propolis samples and Their Activity Against Trypanosoma brucei.

Science.gov (United States)

Omar, Ruwida; Igoli, John O; Zhang, Tong; Gray, Alexander I; Ebiloma, Godwin U; Clements, Carol J; Fearnley, James; Edrada Ebel, RuAngeli; Paget, Tim; de Koning, Harry P; Watson, David G

2017-04-19

Profiling of extracts from twelve propolis samples collected from eight regions in Nigeria was carried out using high performance liquid chromatography (LC) coupled with evaporative light scattering (ELSD), ultraviolet detection (UV) and mass spectrometry (MS), gas chromatography mass spectrometry (GC-MS) and nuclear magnetic resonance spectroscopy (NMR). Principal component analysis (PCA) of the processed LC-MS data demonstrated the varying chemical composition of the samples. Most of the samples were active against Trypanosoma b. brucei with the highest activity being in the samples from Southern Nigeria. The more active samples were fractionated in order to isolate the component(s) responsible for their activity using medium pressure liquid chromatography (MPLC). Three xanthones, 1,3,7-trihydroxy-2,8-di-(3-methylbut-2-enyl)xanthone, 1,3,7-trihydroxy-4,8-di-(3-methylbut-2-enyl)xanthone a previously undescribed xanthone and three triterpenes: ambonic acid, mangiferonic acid and a mixture of α-amyrin with mangiferonic acid (1:3) were isolated and characterised by NMR and LC-MS. These compounds all displayed strong inhibitory activity against T.b. brucei but none of them had higher activity than the crude extracts. Partial least squares (PLS) modelling of the anti-trypanosomal activity of the sample extracts using the LC-MS data indicated that high activity in the extracts, as judged from LCMS 2 data, could be correlated to denticulatain isomers in the extracts.

Multielement analysis of environmental samples by total-reflection X-ray fluorescence sprectrometry, neutron activation analysis and inductively coupled plasma optical emission spectroscopy

International Nuclear Information System (INIS)

Michaelis, W.

1986-01-01

In environmental research and protection trace elements have to be determined over a wide range of atomic number, down to very low concentrations, and in quite different matrices. This challenge requires the availability of complementary analytical methods characterized by a high detection power and few sources of systematic errors. Besides, the capacity of multielement detection is often desired since it facilitates the talking of many problems in which numerous trace elements are of direct concern. Total-reflection X-ray fluorescence, neutron activation analysis and inductively coupled plasma optical emission spectroscopy, in principle fulfill these requirements quite well. However, each method has its domain, and the application to certain sample species may be less promising. Under this aspect, the paper summarizes some recent developments and investigations, including intercomparisons as far as possible. Various matrices are considered : rainwater and airborne particulates, soil samples, river sediments and suspended particulate matter, river water filtrates, ozean water, and organic matrices. Capabilities and limitations are discussed. Sample preparation techniques are described if they are new or essential for achieving the results given. (orig.) [de

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

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

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)

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)

Instrumental activation analysis of molybdenites

International Nuclear Information System (INIS)

Geisler, M.; Schelhorn, H.

1981-01-01

Na, K, Sc, Cr, Fe, Co, Se, Rb, Ag, Cs, Ba, La, Ce, Eu, Yb, Hf, W, Re, and Th have been determined in 6 molybdenite samples by instrumental activation analysis. The samples were of different origin and showed K, Sc, W, and Re values with differences of more than two orders of magnitude, whereas Sc values were within one order of magnitude

X-ray and nuclear methods for comparative analysis of environmental samples

International Nuclear Information System (INIS)

Kudryashov, V.I.; Gundorina, S.F.; Frontas'eva, M.V.; Saidmuradov, Zh.

1988-01-01

X-ray and instrumental neutron activation methods, and in some cases methods of photon activation (X-ray spectral analysis with proton activation and analysis on the basis of (p, n) reaction) were used to obtain elementary content of different water samples. The possibility of getting space-time dependences of trace elementary concentrations in water (and under certain conditions in atmosphere) is shown. These data are to be used at a complex investigation of sanitary norms of water systems. The advantages of abovementined methods are discussed for obtaining different elementary content in water in different ways

Analysis of Cl, Mn, Na, Zn in Food Samples by a Neutron Activation Analysis

International Nuclear Information System (INIS)

Moon, Jong Hwa; Kim, Sun Ha; Chung, Yong Sam; Lee, Ok Hee

2008-01-01

Due to their westernized dietary habit, Korean children are still threatened by the increasing risks of chronic disease such as obesity, hypertension, low immunity, etc. In addition, they are often exposed to a deficiency of Ca, Mg, Fe and micro-minerals which are necessary for their growth, immunity, and prevention of anemia. Nonetheless, the nutritional adequacy of mineral intakes for children is difficult to assess because of a lack of related studies and a nutritional database with respect to Korean children's foods. In this study, ninety kinds of foods consisting of lunch meals from an elementary and a middle school and children's favorite snacks were collected and prepared for an analysis. INAA which has an advantage of a non-destructive technique was employed to determine the elements like Cl, Mn, Na, Cl in the pretreated food samples. Quality control was carried out by using certified reference materials. From the analytical results, elemental concentration range in the collected samples according to the food groups was summarized

Trace elements and As speciation analysis of fly ash samples from an Indonesian coal power plant by means of neutron activation analysis and synchrotron based techniques

International Nuclear Information System (INIS)

Muhayatun Santoso; Diah Dwiana Lestiani; Endah Damastuti; Syukria Kurniawat; Bennett, J.W.; Juan Jose Leani; Mateusz Czyzycki; Alessandro Migliori; Germanos Karydas, Andreas

2016-01-01

The elemental characterization of coal fly ash samples is required to estimate the coal burning emissions into the environment and to assess the potential impact into the biosphere. Fly ash samples collected from a coal fired power plant in center Java, Indonesia were characterized by instrumental neutron activation analysis at two different facilities (BATAN, ANSTO) and synchrotron based techniques at Elettra Italy. Assessment of thirty (30) elements and an investigation of the potential toxicity of As species in coal fly ash were presented. The results obtained are discussed and compared with those reported from other regions of the world. (author)

Activation analysis of rare-earth elements in opium and cannabis samples

International Nuclear Information System (INIS)

Henke, G.

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 13 n cm -2 sec -1 . Cooling period 2-3 days. After addition of 0.1 μCi 139 Ce and rare-earth carriers wet ashing of irradiated samples with H 2 SO 4 /HNO 3 , followed by alternate addition of HNO 3 and H 2 O 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. (T.G.)

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)

Analysis of Waste Isolation Pilot Plant Samples: Integrated Summary Report

Energy Technology Data Exchange (ETDEWEB)

Britt, Phillip F [ORNL

2015-03-01

Analysis of Waste Isolation Pilot Plant Samples: Integrated Summary Report. Summaries of conclusions, analytical processes, and analytical results. Analysis of samples taken from the Waste Isolation Pilot Plant (WIPP) near Carlsbad, New Mexico in support of the WIPP Technical Assessment Team (TAT) activities to determine to the extent feasible the mechanisms and chemical reactions that may have resulted in the breach of at least one waste drum and release of waste material in WIPP Panel 7 Room 7 on February 14, 2014. This report integrates and summarizes the results contained in three separate reports, described below, and draws conclusions based on those results. Chemical and Radiochemical Analyses of WIPP Samples R-15 C5 SWB and R16 C-4 Lip; PNNL-24003, Pacific Northwest National Laboratory, December 2014 Analysis of Waste Isolation Pilot Plant (WIPP) Underground and MgO Samples by the Savannah River National Laboratory (SRNL); SRNL-STI-2014-00617; Savannah River National Laboratory, December 2014 Report for WIPP UG Sample #3, R15C5 (9/3/14); LLNL-TR-667015; Lawrence Livermore National Laboratory, January 2015 This report is also contained in the Waste Isolation Pilot Plant Technical Assessment Team Report; SRNL-RP-2015-01198; Savannah River National Laboratory, March 17, 2015, as Appendix C: Analysis Integrated Summary Report.

Final Sampling and Analysis Plan for Background Sampling, Fort Sheridan, Illinois

National Research Council Canada - National Science Library

1995-01-01

.... This Background Sampling and Analysis Plan (BSAP) is designed to address this issue through the collection of additional background samples at Fort Sheridan to support the statistical analysis and the Baseline Risk Assessment (BRA...

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

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)

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

Sampling and analysis plan for the former Atomic Energy Commission bus lot property

International Nuclear Information System (INIS)

Nielson, R.R.

1998-07-01

This sampling and analysis plan (SAP) presents the rationale and strategy for the sampling and analysis activities proposed in support of an initial investigation of the former Atomic Energy Commission (AEC) bus lot property currently owned by Battelle Memorial Institute. The purpose of the proposed sampling and analysis activity is to investigate the potential for contamination above established action levels. The SAP will provide defensible data of sufficient quality and quantity to support recommendations of whether any further action within the study area is warranted. To assist in preparing sampling plans and reports, the Washington State Department of Ecology (Ecology) has published Guidance on Sampling and Data Analysis Methods. To specifically address sampling plans for petroleum-contaminated sites, Ecology has also published Guidance for Remediation of Petroleum Contaminated Sites. Both documents were used as guidance in preparing this plan. In 1992, a soil sample was taken within the current study area as part of a project to remove two underground storage tanks (USTs) at Battelle's Sixth Street Warehouse Petroleum Dispensing Station (Section 1.3). The results showed that the sample contained elevated levels of total petroleum hydrocarbons (TPH) in the heavy distillate range. This current study was initiated in part as a result of that discovery. The following topics are considered: the historical background of the site, current site conditions, previous investigations performed at the site, an evaluation based on the available data, and the contaminants of potential concern (COPC)

Sampling and analysis plan for the former Atomic Energy Commission bus lot property

Energy Technology Data Exchange (ETDEWEB)

Nielson, R.R.

1998-07-01

This sampling and analysis plan (SAP) presents the rationale and strategy for the sampling and analysis activities proposed in support of an initial investigation of the former Atomic Energy Commission (AEC) bus lot property currently owned by Battelle Memorial Institute. The purpose of the proposed sampling and analysis activity is to investigate the potential for contamination above established action levels. The SAP will provide defensible data of sufficient quality and quantity to support recommendations of whether any further action within the study area is warranted. To assist in preparing sampling plans and reports, the Washington State Department of Ecology (Ecology) has published Guidance on Sampling and Data Analysis Methods. To specifically address sampling plans for petroleum-contaminated sites, Ecology has also published Guidance for Remediation of Petroleum Contaminated Sites. Both documents were used as guidance in preparing this plan. In 1992, a soil sample was taken within the current study area as part of a project to remove two underground storage tanks (USTs) at Battelle`s Sixth Street Warehouse Petroleum Dispensing Station (Section 1.3). The results showed that the sample contained elevated levels of total petroleum hydrocarbons (TPH) in the heavy distillate range. This current study was initiated in part as a result of that discovery. The following topics are considered: the historical background of the site, current site conditions, previous investigations performed at the site, an evaluation based on the available data, and the contaminants of potential concern (COPC).

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

Ground-water sample collection and analysis plan for the ground-water surveillance project

International Nuclear Information System (INIS)

Bryce, R.W.; Evans, J.C.; Olsen, K.B.

1991-12-01

The Pacific Northwest Laboratory performs ground-water sampling activities at the US Department of Energy's (DOE's) Hanford Site in support of DOE's environmental surveillance responsibilities. The purpose of this document is to translate DOE's General Environmental Protection Program (DOE Order 5400.1) into a comprehensive ground-water sample collection and analysis plan for the Hanford Site. This sample collection and analysis plan sets forth the environmental surveillance objectives applicable to ground water, identifies the strategy for selecting sample collection locations, and lists the analyses to be performed to meet those objectives

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)

Elemental composition of platelets. Part I. Sampling and sample preparation of platelets for trace-element analysis

International Nuclear Information System (INIS)

Iyengar, G.V.; Borberg, H.; Kasperek, K.; Kiem, J.; Siegers, M.; Feinendegen, L.E.; Gross, R.

1979-01-01

Sampling of platelets for trace-element analysis poses special problems: obtaining adequate sample materials, achieving a sufficient cell purity, preserving viability (integrity), correcting for trapped plasma, and controlling contamination. We used a blood-cell separator for the primary isolation of platelets from blood, and differential centrifugation in natural plasma to further isolate them. The pyrimidopyrimidine RA233 was used as a stabilizer to maintain viability. 131 I-labeled human serum albumin was used to estimate trapped plasma. Contamination was controlled by using five-times-distilled water to simulate donor's blood in the system and by comparing three fractions: the serum, the first portion of the platelet-rich plasma, and the supernatant plasma after the final centrifugation. Neutron activation analysis was used for the elemental analysis. A single differential centrifugation of the platelet-rich plasma from the blood-cell separator at 400 x g for 8 min was optimum (mean mass fractions: erythrocytes/platelets < 5 mg/g and leukocytes/platelets < 20 mg/g). The trapped plasma in the wet platelet samples amounted to about 0.40 g/g. No appreciable contamination from the sampling system was found for the elements Ag, Cd, Co, Cr, Cs, Cu, Fe, Mo, Rb, Sb, Se, and Zn. 2 figures, 3 tables

Microextraction sample preparation techniques in biomedical analysis.

Science.gov (United States)

Szultka, Malgorzata; Pomastowski, Pawel; Railean-Plugaru, Viorica; Buszewski, Boguslaw

2014-11-01

Biologically active compounds are found in biological samples at relatively low concentration levels. The sample preparation of target compounds from biological, pharmaceutical, environmental, and food matrices is one of the most time-consuming steps in the analytical procedure. The microextraction techniques are dominant. Metabolomic studies also require application of proper analytical technique for the determination of endogenic metabolites present in biological matrix on trace concentration levels. Due to the reproducibility of data, precision, relatively low cost of the appropriate analysis, simplicity of the determination, and the possibility of direct combination of those techniques with other methods (combination types on-line and off-line), they have become the most widespread in routine determinations. Additionally, sample pretreatment procedures have to be more selective, cheap, quick, and environmentally friendly. This review summarizes the current achievements and applications of microextraction techniques. The main aim is to deal with the utilization of different types of sorbents for microextraction and emphasize the use of new synthesized sorbents as well as to bring together studies concerning the systematic approach to method development. This review is dedicated to the description of microextraction techniques and their application in biomedical analysis. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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.)

Analysis of Cl, Mn, Na, Zn in Food Samples by a Neutron Activation Analysis

Energy Technology Data Exchange (ETDEWEB)

Moon, Jong Hwa; Kim, Sun Ha; Chung, Yong Sam [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of); Lee, Ok Hee [YongIn University, Yongin (Korea, Republic of)

2008-10-15

Due to their westernized dietary habit, Korean children are still threatened by the increasing risks of chronic disease such as obesity, hypertension, low immunity, etc. In addition, they are often exposed to a deficiency of Ca, Mg, Fe and micro-minerals which are necessary for their growth, immunity, and prevention of anemia. Nonetheless, the nutritional adequacy of mineral intakes for children is difficult to assess because of a lack of related studies and a nutritional database with respect to Korean children's foods. In this study, ninety kinds of foods consisting of lunch meals from an elementary and a middle school and children's favorite snacks were collected and prepared for an analysis. INAA which has an advantage of a non-destructive technique was employed to determine the elements like Cl, Mn, Na, Cl in the pretreated food samples. Quality control was carried out by using certified reference materials. From the analytical results, elemental concentration range in the collected samples according to the food groups was summarized.

UMTRA Project water sampling and analysis plan, Salt Lake City, Utah. Revision 1

International Nuclear Information System (INIS)

1995-06-01

This water sampling and analysis plan describes planned, routine ground water sampling activities at the US Department of Energy Uranium Mill Tailings Remedial Action Project site in Salt Lake City, Utah. This plan identifies and justifies sampling locations, analytical parameters, detection limits, and sampling frequencies for routine monitoring of ground water, sediments, and surface waters at monitoring stations on the site

passive and active measurements for some ceramic samples

International Nuclear Information System (INIS)

Hassan, M.F.; Said, S.A.; Ali, M.A.; Szegedi, S.

2004-01-01

passive measurements for an imported natural ore (zirconium silicate) used in ceramic industries were carried out to identify its radioactivity . this work was done for ceramic quality control purposes. accurate gamma spectrometers with 30% and 70% detector efficiencies were used in the measurements. the 235 U, 238 U and 232 Th radioactivity were determined . for the sake of comparison already manufactured different ceramic samples were investigated applying fast neutrons activation analysis (FNAA) and X-Ray florescence (XRF) techniques. the obtained results were discussed with the tabulated international radioactivity levels for building materials

14 MeV proton activation analysis

International Nuclear Information System (INIS)

Constantinescu, B.; Ivanov, E.; Plostinaru, D.; Popa-Nemoiu, A.; Pascovichi, G.

1985-01-01

A fast nuclear nondestructive method for protein analysis using the 14 MeV proton activation has been developed. The total nitrogen content was measured through the reaction: 14 N (p,n) 14 O, (Tsub(1/2)=71 s). The 14 O activity was detected by means of its characteristic 2.312 MeV gamma-ray line with a NaI(Tl) detector. For a fast determination of a large number of samples a mechanized sistem reacting a rate of one sample per minute has been developed. The laboratory electronics comprises a multichannel analyser, a PDP computer and an electronic module comtroller. Comparison of the results obtained by the method described and the classical Kjeldal technique for samples of various cereal grains (soya bean seads, wheat, barley and corn) showed good correlation. A problem of the analysis of the whole protein region on corn and soya-bean seads, where this region is thicker (0,2 - 2 mm), is mentioned. In this case flour was proposed to be used to obtain a protein homogeneous sample and the irradiaton dose for a sample was about 33,000 Gy, mainly (99%) from protons (27 s x 100 nA x 14 MeV)

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.).

105-DR Large Sodium Fire Facility decontamination, sampling, and analysis plan

International Nuclear Information System (INIS)

Knaus, Z.C.

1995-01-01

This is the decontamination, sampling, and analysis plan for the closure activities at the 105-DR Large Sodium Fire Facility at Hanford Reservation. This document supports the 105-DR Large Sodium Fire Facility Closure Plan, DOE-RL-90-25. The 105-DR LSFF, which operated from about 1972 to 1986, was a research laboratory that occupied the former ventilation supply room on the southwest side of the 105-DR Reactor facility in the 100-D Area of the Hanford Site. The LSFF was established to investigate fire fighting and safety associated with alkali metal fires in the liquid metal fast breeder reactor facilities. The decontamination, sampling, and analysis plan identifies the decontamination procedures, sampling locations, any special handling requirements, quality control samples, required chemical analysis, and data validation needed to meet the requirements of the 105-DR Large Sodium Fire Facility Closure Plan in compliance with the Resource Conservation and Recovery Act

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)

Tank 241-SY-101 push mode core sampling and analysis plan

International Nuclear Information System (INIS)

CONNER, J.M.

1998-01-01

This sampling and analysis plan (SAP) identifies characterization objectives pertaining to sample collection, laboratory analytical evaluation, and reporting requirements for push mode core samples from tank 241-SY-101 (SY-101). It is written in accordance with Data Quality Objective to Support Resolution of the Flammable Gas Safety Issue (Bauer 1998), Low Activity Waste Feed Data Quality Objectives (Wiemers and Miller 1997 and DOE 1998), Data Quality Objectives for TWRS Privatization Phase I: Confirm Tank T is an Appropriate Feed Source for Low-Activity Waste Feed Batch X (Certa 1998), and the Tank Safety Screening Data Quality Objective (Dukelow et al. 1995). The Tank Characterization Technical Sampling Basis document (Brown et al. 1998) indicates that these issues apply to tank SY-101 for this sampling event. Brown et al. also identifies high-level waste, regulatory, pretreatment and disposal issues as applicable issues for this tank. However, these issues will not be addressed via this sampling event

Determination of concentrations of minor and micro elements in ancient bronze drums artifacts samples by KO-standardization method of neutron activation analysis

International Nuclear Information System (INIS)

Nguyen Tac Anh; Ho Manh Dung; Diep Dinh Hoa; Cao Dong Vu

2000-01-01

The study aims to get a lot information about manufacturers of ancient bronze artifacts and ancient civilization. By KO-standardization method of neutron activation analysis developed in the Nuclear Research Institute, the concentrations of Au, Ag, As, Zn, Sb, Sn elements in ancient bronze alloy samples of 99 bronze artifacts from many excavated archaeological sites at the provinces in Vietnam were determined with uncertainties about ±10%. These elemental concentrations have been utilized in a statistical analysis procedure in order to determine similarities and correlation between the various samples. Th abnormal high of concentrations of noble metals as Au, Ag in ancient bronze indicates that the ancient metallurgists had been interested in role of these metals on sound quality of bronze artifacts. Especially, the concentrations of As in many samples are very high even at about 10%. This gives an evidence that in ancient time the humankind could use bronze As alloy in order to improve quality when they had produced bronze artifacts. (author)

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

Analysis of mercury in environmental samples

International Nuclear Information System (INIS)

Schoester, F.S.

1992-01-01

The possibility to determine mercury in sub-ppm levels in biological samples has been studied through neutron activation analysis , using as standards aliquots of mercury nitrate solution, deposited on treated cellulose with thio acetamide and ammonia. Sample and standards were irradiated simultaneously in quartz ampoules during 8 hours at a flux of 5 x 10 13 n/cm 2 s and were counted in a hyper pure germanium detector after 4 weeks of decay. Corrections were made for the interference of 75 Se in the 279 keV photopeak used in the determination. The results obtained for the reference materials IAEA-H-8(horse kidney), IAEA-M A-A2(fish flesh) and IAEA-M A-A-1(cope pod homogenate) were (0.91±0.07), (0.56±0.02) and (0.17±0.02) ppm, versus certified values of (0.91±0.08), (0.47±0.02) and (0.28±0.01) ppm respectively. (EMR). 54 refs., 8 app

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

Pneumatic transport devices based on the ARS equipment set for activation analysis

International Nuclear Information System (INIS)

Ivanov, I.V.; Ivanets, V.N.; Rogachev, V.M.; Zakharov, E.A.

1978-01-01

The AGIDEL and ARS-28G facilities manufactured on the basis of a set of standardized and aggregated products for activation analysis are described. The AGIDEL is designed for automatic activation analysis of relatively homogeneous samples from oil boreholes. The ARS-28G is designed for transporting the test samples during activation analysis, using a fast-neutron generator. Structurally, the ARS-28 is based on a pneumatic transportation system with two independenhat transport cnnels and a two-channel rotating irradiation unit. The analyzed samples are transported in polyethylene containers, which are moved by compressed air. The facility has been successfully tested and is used in an automated system for multielement activation analysis

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

7th international conference ''Modern trends in activation analysis''

International Nuclear Information System (INIS)

Obrusnik, I.

1987-01-01

The conference was held on 23-27 June, 1986 in Copenhagen (DK) with the participation of specialists from 42 countries. 175 papers were submitted covering the wide field of applications of neutron activation analysis, from novel techniques to sample preparation, information processes and control, activation techniques, light element and rare earth element determination, ultratracer analysis, quality assurance, comparator methods, and reference materials. The poster session was mainly oriented to industrial applications of activation analysis, biological applications, in vivo use of neutron activation analysis, the applications of neutron activation analysis in environmental control, criminology, etc. (E.S.)

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

Sampling frequency affects ActiGraph activity counts

DEFF Research Database (Denmark)

Brønd, Jan Christian; Arvidsson, Daniel

that is normally performed at frequencies higher than 2.5 Hz. With the ActiGraph model GT3X one has the option to select sample frequency from 30 to 100 Hz. This study investigated the effect of the sampling frequency on the ouput of the bandpass filter.Methods: A synthetic frequency sweep of 0-15 Hz was generated...... in Matlab and sampled at frequencies of 30-100 Hz. Also, acceleration signals during indoor walking and running were sampled at 30 Hz using the ActiGraph GT3X and resampled in Matlab to frequencies of 40-100 Hz. All data was processed with the ActiLife software.Results: Acceleration frequencies between 5......-15 Hz escaped the bandpass filter when sampled at 40, 50, 70, 80 and 100 Hz, while this was not the case when sampled at 30, 60 and 90 Hz. During the ambulatory activities this artifact resultet in different activity count output from the ActiLife software with different sampling frequency...

OpenMSI Arrayed Analysis Toolkit: Analyzing Spatially Defined Samples Using Mass Spectrometry Imaging

Energy Technology Data Exchange (ETDEWEB)

de Raad, Markus [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); de Rond, Tristan [Univ. of California, Berkeley, CA (United States); Rübel, Oliver [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Keasling, Jay D. [Univ. of California, Berkeley, CA (United States); Joint BioEnergy Inst. (JBEI), Emeryville, CA (United States); Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Technical Univ. of Denmark, Lyngby (Denmark); Northen, Trent R. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); USDOE Joint Genome Institute (JGI), Walnut Creek, CA (United States); Bowen, Benjamin P. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); USDOE Joint Genome Institute (JGI), Walnut Creek, CA (United States)

2017-05-03

Mass spectrometry imaging (MSI) has primarily been applied in localizing biomolecules within biological matrices. Although well-suited, the application of MSI for comparing thousands of spatially defined spotted samples has been limited. One reason for this is a lack of suitable and accessible data processing tools for the analysis of large arrayed MSI sample sets. In this paper, the OpenMSI Arrayed Analysis Toolkit (OMAAT) is a software package that addresses the challenges of analyzing spatially defined samples in MSI data sets. OMAAT is written in Python and is integrated with OpenMSI (http://openmsi.nersc.gov), a platform for storing, sharing, and analyzing MSI data. By using a web-based python notebook (Jupyter), OMAAT is accessible to anyone without programming experience yet allows experienced users to leverage all features. OMAAT was evaluated by analyzing an MSI data set of a high-throughput glycoside hydrolase activity screen comprising 384 samples arrayed onto a NIMS surface at a 450 μm spacing, decreasing analysis time >100-fold while maintaining robust spot-finding. The utility of OMAAT was demonstrated for screening metabolic activities of different sized soil particles, including hydrolysis of sugars, revealing a pattern of size dependent activities. Finally, these results introduce OMAAT as an effective toolkit for analyzing spatially defined samples in MSI. OMAAT runs on all major operating systems, and the source code can be obtained from the following GitHub repository: https://github.com/biorack/omaat.

Instrumental neutron activation analysis as a routine method for rock analysis

International Nuclear Information System (INIS)

Rosenberg, R.J.

1977-06-01

Instrumental neutron activation methods for the analysis of geological samples have been developed. Special emphasis has been laid on the improvement of sensitivity and accuracy in order to maximize tha quality of the analyses. Furthermore, the procedures have been automated as far as possible in order to minimize the cost of the analysis. A short review of the basic literature is given followed by a description of the principles of the method. All aspects concerning the sensitivity are discussed thoroughly in view of the analyst's possibility of influencing them. Experimentally determined detection limits for Na, Al, K, Ca, Sc, Cr, Ti, V, Mn, Fe, Ni, Co, Rb, Zr, Sb, Cs, Ba, La, Ce, Nd, Sm, Eu, Gd, Tb, Dy, Yb, Lu, Hf, Ta, Th and U are given. The errors of the method are discussed followed by actions taken to avoid them. The most significant error was caused by flux deviation, but this was avoided by building a rotating sample holder for rotating the samples during irradiation. A scheme for the INAA of 32 elements is proposed. The method has been automated as far as possible and an automatic γ-spectrometer and a computer program for the automatic calculation of the results are described. Furthermore, a completely automated uranium analyzer based on delayed neutron counting is described. The methods are discussed in view of their applicability to rock analysis. It is stated that the sensitivity varies considerably from element to element and instrumental activation analysis is an excellent method for the analysis of some specific elements like lanthanides, thorium and uranium but less so for many other elements. The accuracy is good varying from 2% to 10% for most elements. Instrumental activation analysis for most elements is rather an expensive method there being, however, a few exceptions. The most important of these is uranium. The analysis of uranium by delayed neutron counting is an inexpensive means for the analysis of large numbers of samples needed for

105-N Basin sediment disposition phase-one sampling and analysis plan

International Nuclear Information System (INIS)

1997-01-01

The sampling and analysis plan (SAP) for Phase 1 of the 105-N Basin sediment disposition project defines the sampling and analytical activities that will be performed for the engineering assessment phase (phase 1) of the project. A separate SAP defines the sampling and analytical activities that will be performed for the characterization phase (Phase 2) of the 105-N sediment disposition project. The Phase-1 SAP is presented in the introduction (Section 1.0), in the field sampling plan (FSP) (Section 2.0), and in the quality assurance project plan (QAPjP) (Section 3.0). The FSP defines the sampling and analytical methodologies to be performed. The QAPjP provides information on the quality assurance/quality control (QA/QC) parameters related to the sampling and analytical methodologies. This SAP defines the strategy and the methods that will be used to sample and analyze the sediment on the floor of the 105-N Basin. The resulting data will be used to develop and evaluate engineering designs for collecting and removing sediment from the basin

Sampling and analysis plan for remediation of Operable Unit 100-IU-3 waste site 600-104. Revision 1

International Nuclear Information System (INIS)

1997-08-01

This sampling and analysis plan presents the rationale and strategy for the sampling and analysis activities to support remediation of 100-IU-3 Operable Unit waste site 600-104. The purpose of the proposed sampling and analysis activities is to demonstrate that time-critical remediation of the waste site for soil containing 2,4-Dichlorophenoxyacetic acid salts and esters (2,4-D) and dioxin/furan isomers at concentrations that exceed cleanup levels has been effective. This shall be accomplished by sampling various locations of the waste site before and after remediation, analyzing the samples, and comparing the results to action levels set by the Washington State Department of Ecology

A description of the BNL active surface analysis facility

International Nuclear Information System (INIS)

Tyler, J.W.

1989-11-01

Berkeley Nuclear Laboratories has a responsibility for the assessment of radioactive specimens arising both from post irradiation examination of power reactor components and structures and experimental programmes concerned with fission and activation product transport. Existing analytical facilities have been extended with the commissioning of an active surface analysis instrument (XSAM 800pci, Kratos Analytical). Surface analysis involves the characterisation of the outer few atomic layers of a solid surface/interface whose chemical composition and electronic structure will probably be different from the bulk. The new instrument consists three interconnected chambers positioned in series; comprising of a high vacuum sample introduction chamber, an ultra-high vacuum sample treatment/fracture chamber and an ultra-high vacuum sample analysis chamber. The sample analysis chamber contains the electron, X-ray and ion-guns and the electron and ion detectors necessary for performing X-ray photoelectron spectroscopy, scanning Auger microscopy and secondary-ion mass spectroscopy. The chamber also contains a high stability manipulator to enable sub-micron imaging of specimens to be achieved and provide sample heating and cooling between - 180 and 600 0 C. (author)

Activation analysis and classification to source of samples from the Kimberley Reef Conglomerates

International Nuclear Information System (INIS)

Rasmussen, S.E.

1977-01-01

Three boreholes were drilled in the west, central, and eastern sections of the Durban Roodepoort Deep Mine, and twelve distinct strata were intersected. Twenty-two samples from the three borehole cores were analysed in triplicate for twenty-six elements, and, including standards, a total of 2000 determinations were made. Statistical analysis of the results obtained for twenty-four elements shows a successful back-classification of 98 per cent, whereas, if the conglomerates or quartzites are treated separately, 100 per cent success is obtained. When the present data are used for classification of the samples from the three cores analysed during the first phase of this project, 100 per cent accuracy of classification is achieved by use of only ten selected elements. The objects of this investigation have therefore been met successfully, and extension to further strata and to sampling beyond the confines of the mine is justified [af

Charged-particle activation analysis

International Nuclear Information System (INIS)

Schweikert, E.A.

1978-01-01

The paper discusses the methodology and application of nuclear activation with ion beams (1 9 via 16 O( 3 He,p) 18 F, 12 C( 3 He,α) 11 C and 14 N(p,α) 11 C respectively. Recently, triton activation has been shown to be inherently still superior to 3 He activation for the determination of oxygen [ 16 O( 3 H,n) 18 F]. Lithium, boron, carbon and sulphur can be detected rapidly, nondestructively and with high sensitivity (approximately 0.25ppm for Li and B) via ''quasi-prompt'' activation based on the detection of short-lived, high-energy beta emitters (10ms 1 H( 7 Li,n) 7 Be for example. Nondestructive multielement analysis: Proton activation has the inherent potential for meeting requirements of broad elemental coverage, sensitivity (ppm and sub-ppm range) and selectivity. Up to 30 elements have been determined in Al, Co, Ag, Nb, Rh, Ta and biological samples, using 12-MeV proton activation followed by gamma-ray spectrometry. These capabilities are further enhanced with the counting of X-ray emitters, 28 elements (26 9 ) and accuracy using proton activation. 204 Pb/ 206 Pb ratios can also be determined with a relative precision of a few per cent. Although charged-particle activation analysis is a well-established trace analysis technique, broad potential capabilities remain to be explored, e.g. those arising from ultrashort-lived nuclides, heavy ion interactions and the combination of delayed and prompt methods. (author)

Is activation analysis still active?

International Nuclear Information System (INIS)

Chai Zhifang

2001-01-01

This paper reviews some aspects of neutron activation analysis (NAA), covering instrumental neutron activation analysis (INAA), k 0 method, prompt gamma-ray neutron activation analysis (PGNAA), radiochemical neutron activation analysis (RNAA) and molecular activation analysis (MAA). The comparison of neutron activation analysis with other analytical techniques are also made. (author)

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.

Specific activity of 129I in environmental samples

International Nuclear Information System (INIS)

Ravi, P.M.; Iyer, M.R.; Bhat, I.S.; Somasundaram, S.; Subramanian, M.S.

1988-01-01

129 I finds its way into the environment as a result of man-made nuclear operations. It is also formed by the interaction of cosmic rays with xenon isotopes and spontaneous fission of naturally occurring uranium. 129 I and stable 127 I contents of thyroid, milk, seaweed and aplysia cell samples collected from around a fuel reprocessing plant were estimated by neutron activation analysis method. The annual 129 I intake of an individual works out to be about 0.3 Bq as compared to the natural radioactivity content in human body of about 5000 Bq. (author). 3 tabs

Sensitivity Range Analysis of Infrared (IR) Transmitter and Receiver Sensor to Detect Sample Position in Automatic Sample Changer

International Nuclear Information System (INIS)

Syirrazie Che Soh; Nolida Yussup; Nur Aira Abdul Rahman; Maslina Ibrahim

2016-01-01

Sensitivity range of IR Transmitter and Receiver Sensor influences the effectiveness of the sensor to detect position of a sample. Then the purpose of this analysis is to determine the suitable design and specification the electronic driver of the sensor to gain appropriate sensitivity range for required operation. The related activities to this analysis cover electronic design concept and specification, calibration of design specification and evaluation on design specification for required application. (author)

NID Copper Sample Analysis

Energy Technology Data Exchange (ETDEWEB)

Kouzes, Richard T.; Zhu, Zihua

2011-09-12

The current focal point of the nuclear physics program at PNNL is the MAJORANA DEMONSTRATOR, and the follow-on Tonne-Scale experiment, a large array of ultra-low background high-purity germanium detectors, enriched in 76Ge, designed to search for zero-neutrino double-beta decay (0νββ). This experiment requires the use of germanium isotopically enriched in 76Ge. The MAJORANA DEMONSTRATOR is a DOE and NSF funded project with a major science impact. The DEMONSTRATOR will utilize 76Ge from Russia, but for the Tonne-Scale experiment it is hoped that an alternate technology, possibly one under development at Nonlinear Ion Dynamics (NID), will be a viable, US-based, lower-cost source of separated material. Samples of separated material from NID require analysis to determine the isotopic distribution and impurities. DOE is funding NID through an SBIR grant for development of their separation technology for application to the Tonne-Scale experiment. The Environmental Molecular Sciences facility (EMSL), a DOE user facility at PNNL, has the required mass spectroscopy instruments for making isotopic measurements that are essential to the quality assurance for the MAJORANA DEMONSTRATOR and for the development of the future separation technology required for the Tonne-Scale experiment. A sample of isotopically separated copper was provided by NID to PNNL in January 2011 for isotopic analysis as a test of the NID technology. The results of that analysis are reported here. A second sample of isotopically separated copper was provided by NID to PNNL in August 2011 for isotopic analysis as a test of the NID technology. The results of that analysis are also reported here.

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

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)

Activation analysis with small mobile reactors

International Nuclear Information System (INIS)

Chung, C.

1990-01-01

A small nuclear reactor (a low-power reactor without heat removal devices) usually has thermal power output under 100 W and an average in-core thermal neutron flux below 10 9 n/cm 2 s. Conventional activation analysis is restricted to determination of specific elements with large neutron capture cross sections in sizable samples. In-vivo prompt gamma activation analysis (IVPGAA) can be used for diagnosis of elemental composition of the human body, particularly the essential elements Ca, Cl, N, and P in the whole body, and toxic Cd and Hg in contaminated organs. In this chapter, activation analysis using an external neutron beam from the Tsing Hua Mobile Educational Reactor (THMER) for in vivo activation is described. Characteristics of the mobile reactor, in-vivo medical diagnosis, and radiation safety are emphasized. 17 refs, 12 figs, 3 tabs

Analysis of 137Cs radionuclides activities in Cs-zeolite using gamma spectrometry

International Nuclear Information System (INIS)

Noviarty; Ginting, Aslina Br; Anggraini, Dian; Rosika K

2013-01-01

137 Cs Radionuclide activity analysis has been carried out. The objective is to determine the activity of the 137 Cs radionuclide in Cs-zeolite are packaged in the form of point source. Analysis of 137 Cs Radionuclide activities in Cs zeolite samples was determined by measuring intensity of the isotope 137 Cs gamma energy at 661.7 keV use-y spectrometer. Before measurement the sample, was first carried out measurements of 137 Cs radionuclide in certified point standards from Amersham, to determine the efficiency value. Result the standard sample measurement obtained the efficiency value of 43.98%. Efficiency values obtained are used in the calculation of sample activity. On the measurement of the intensity of the sample obtained results dose rate 196.4537 cps with a standard deviation of 0.5274. By using standard measurement efficiency values obtained by the calculation of the average activity of the radionuclide 137 Cs in Cs-zeolite 524.9082 Bq. Deviation measurements were below 5% (0.27% ) so that the analysis of the activity of radionuclide 137 Cs in Cs-zeolite samples using gamma spectrometer can be accepted with a 95% confidence level. (author)

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

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)

Nonradioactive Dangerous Waste Landfill sampling and analysis plan and data quality objectives process summary report

International Nuclear Information System (INIS)

Smith, R.C.

1997-08-01

This sampling and analysis plan defines the sampling and analytical activities and associated procedures that will be used to support the Nonradioactive Dangerous Waste Landfill soil-gas investigation. This SAP consists of three sections: this introduction, the field sampling plan, and the quality assurance project plan. The field sampling plan defines the sampling and analytical methodologies to be performed

Uranium-233 analysis of biological samples

International Nuclear Information System (INIS)

Gies, R.A.; Ballou, J.E.; Case, A.C.

1979-01-01

Two liquid scintillation techniques were compared for 233 U analysis: a two-phase extraction system (D2EHPA) developed by Keough and Powers, 1970, for Pu analysis; and a single-phase emulsion system (TT21) that holds the total sample in suspension with the scintillator. The first system (D2EHPA) was superior in reducing background (two- to threefold) and in accommodating a larger sample volume (fivefold). Samples containing > 50 mg/ml of slats were not extracted quantitatively by D2EHPA

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)

A study on antimony determination in environmental samples by neutron activation analysis: validation of the methodology and determination of the uncertainty of the measurement

International Nuclear Information System (INIS)

Matsubara, Tassiane Cristina Martins

2011-01-01

Antimony is an element found in low concentrations in the environment. However, its determination has attracted great interest due to the knowledge of its toxicity and increasing application in industry. The determination of antimony has been a challenge for researchers since this element is found in low concentrations which make its analysis a difficult task. Therefore, although neutron activation analysis (NAA) is an appropriate method for the determination of various elements in different types of matrix, in the case of Sb its analysis presents some difficulties, mainly due to spectral interferences. The objective of this research was to validate the NAA method for Sb determination in environmental samples. To establish appropriate conditions for Sb determinations, preliminary assays were carried out for further analysis of certified reference materials (CRM). The experimental procedure was to irradiate samples with a synthetic Sb standard for a period of 8 or 16 hours in the IEA-R1 nuclear research reactor, followed by gamma ray spectrometry. The quantification of Sb was performed by measuring the radioactive isotopes of 122 Sb and '1 24 Sb. The results of preliminary assays indicated the presence of Sb in Whatman no 40 filter paper used in the preparation of the synthetic standard, but at very low concentrations, which could be considered negligible. In the case of the plastic material used in bags for the sample irradiation, it should be chosen carefully, because depending on the thickness, they may contain Sb. The analyses of the stability of the diluted Sb standard solution showed no change in the Sb concentration within eight months after its preparation. Results obtained in the analysis of certified reference materials indicated the interference of 76 As and also of 134 Cs and 152 Eu in the Sb determinations by measuring '1 22 Sb, due to the proximity of the gamma ray energies. The high activity of '2 4 Na can also mask the peak of 122 Sb hindering its

Activation analysis of ground water of Chandigarh

International Nuclear Information System (INIS)

Mittal, V.K.

1997-01-01

Ground water samples from Chandigarh were analysed for 22 trace elements using neutron activation analysis (NAA) technique. These samples were drawn from shallow aquifers using hand pumps. It was found that for most of the elements the concentrations were well within the ISI/WHO recommended values. However, samples collected from the industrial belt of the city showed higher concentrations of trace elements, particularly some toxic ones. (author). 6 refs., 1 tab

Sampling and Analysis Instruction for the Demolition of the Masonry Block for the 108-F Biological Laboratory

International Nuclear Information System (INIS)

Byrnes, M. E.

1999-01-01

This sampling and analysis instruction (SAI) has been prepared to clearly define the sampling and analysis activities to be performed in support of the demolition and disposition (or disposal) of the 108-F Biological Laboratory masonry block walls

Influence of sampling depth and post-sampling analysis time on the ...

African Journals Online (AJOL)

Bacteriological analysis was carried out for samples taken at water depth and at 1, 6, 12 and 24 hours post-sampling. It was observed that the total and faecal coliform bacteria were significantly higher in the 3 m water depth samples than in the surface water samples (ANOVA, F = 59.41, 26.751, 9.82 (T.C); 46.41, 26.81, ...

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

Enhanced AFCI Sampling, Analysis, and Safeguards Technology Review

Energy Technology Data Exchange (ETDEWEB)

John Svoboda

2009-09-01

The focus of this study includes the investigation of sampling technologies used in industry and their potential application to nuclear fuel processing. The goal is to identify innovative sampling methods using state of the art techniques that could evolve into the next generation sampling and analysis system for metallic elements. Sampling and analysis of nuclear fuel recycling plant processes is required both to monitor the operations and ensure Safeguards and Security goals are met. In addition, environmental regulations lead to additional samples and analysis to meet licensing requirements. The volume of samples taken by conventional means, can restrain productivity while results samples are analyzed, require process holding tanks that are sized to meet analytical issues rather than process issues (and that create a larger facility footprint), or, in some cases, simply overwhelm analytical laboratory capabilities. These issues only grow when process flowsheets propose new separations systems and new byproduct material for transmutation purposes. Novel means of streamlining both sampling and analysis are being evaluated to increase the efficiency while meeting all requirements for information. This report addresses just a part of the effort to develop and study novel methods by focusing on the sampling and analysis of aqueous samples for metallic elements. It presents an overview of the sampling requirements, including frequency, sensitivity, accuracy, and programmatic drivers, to demonstrate the magnitude of the task. The sampling and analysis system needed for metallic element measurements is then discussed, and novel options being applied to other industrial analytical needs are presented. Inductively coupled mass spectrometry instruments are the most versatile for metallic element analyses and are thus chosen as the focus for the study. Candidate novel means of process sampling, as well as modifications that are necessary to couple such instruments to

Materials and Methods for Streamlined Laboratory Analysis of Environmental Samples, FY 2016 Report

Energy Technology Data Exchange (ETDEWEB)

Addleman, Raymond S. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Naes, Benjamin E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); McNamara, Bruce K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Olsen, Khris B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Chouyyok, Wilaiwan [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Willingham, David G. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Spigner, Angel C. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2016-11-30

The International Atomic Energy Agency (IAEA) relies upon laboratory analysis of environmental samples (typically referred to as “swipes”) collected during on-site inspections of safeguarded facilities to support the detection and deterrence of undeclared activities. Unfortunately, chemical processing and assay of the samples is slow and expensive. A rapid, effective, and simple extraction process and analysis method is needed to provide certified results with improved timeliness at reduced costs (principally in the form of reduced labor), while maintaining or improving sensitivity and efficacy. To address these safeguard needs the Pacific Northwest National Laboratory (PNNL) explored and demonstrated improved methods for environmental sample (ES) analysis. Improvements for both bulk and particle analysis were explored. To facilitate continuity and adoption, the new sampling materials and processing methods will be compatible with existing IAEA protocols for ES analysis. PNNL collaborated with Oak Ridge National Laboratory (ORNL), which performed independent validation of the new bulk analysis methods and compared performance to traditional IAEA’s Network of Analytical Laboratories (NWAL) protocol. ORNL efforts are reported separately. This report describes PNNL’s FY 2016 progress, which was focused on analytical application supporting environmental monitoring of uranium enrichment plants and nuclear fuel processing. In the future the technology could be applied to other safeguard applications and analytes related to fuel manufacturing, reprocessing, etc. PNNL’s FY 2016 efforts were broken into two tasks and a summary of progress, accomplishments and highlights are provided below. Principal progress and accomplishments on Task 1, Optimize Materials and Methods for ICP-MS Environmental Sample Analysis, are listed below. • Completed initial procedure for rapid uranium extraction from ES swipes based upon carbonate-peroxide chemistry (delivered to ORNL for

UMTRA project water sampling and analysis plan, Tuba City, Arizona

International Nuclear Information System (INIS)

1996-02-01

Planned, routine ground water sampling activities at the U.S. Department of Energy (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site in Tuba City, Arizona, are described in the following sections of this water sampling and analysis plan (WSAP). This plan identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequency for the stations routinely monitored at the site. The ground water data are used for site characterization and risk assessment. The regulatory basis for routine ground water monitoring at UMTRA Project sites is derived from the U.S. Environmental Protection Agency (EPA) regulations in 40 CFR Part 192 (1994) and the final EPA standards of 1995 (60 FR 2854). Sampling procedures are guided by the UMTRA Project standard operating procedures (SOP) (JEG, n.d.), and the most effective technical approach for the site

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)

Sampling and Analysis Plan for K Basins Debris

International Nuclear Information System (INIS)

WESTCOTT, J.L.

2000-01-01

This Sampling and Analysis Plan presents the rationale and strategy for sampling and analysis activities to support removal of debris from the K-East and K-West Basins located in the 100K Area at the Hanford Site. This project is focused on characterization to support waste designation for disposal of waste at the Environmental Restoration Disposal Facility (ERDF). This material has previously been dispositioned at the Hanford Low-Level Burial Grounds or Central Waste Complex. The structures that house the basins are classified as radioactive material areas. Therefore, all materials removed from the buildings are presumed to be radioactively contaminated. Because most of the materials that will be addressed under this plan will be removed from the basins, and because of the cost associated with screening materials for release, it is anticipated that all debris will be managed as low-level waste. Materials will be surveyed, however, to estimate radionuclide content for disposal and to determine that the debris is not contaminated with levels of transuranic radionuclides that would designate the debris as transuranic waste

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.

Multielemental analysis of milk samples

International Nuclear Information System (INIS)

Omar Al-Dayel; Jameel Al-Hefne; Didarul A Chowdhury; Turki Al-Ajyan

2002-01-01

Milk is a basic food since it provides essential nutrients (proteins, lipids, carbohydrates) and micronutrients (minerals, Vitamins, enzymes). In fact, in formula milk essential elements have been usually added in order to satisfy nutritional requirements. However, too high additions of these elements can produce detrimental effects on human health. More important, milk can also constitute a source of exposure to toxic elements, especially dangerous for infants. Method is presented for the multielemental analysis of a wide range of elements in milk samples. The aim of this work is the development of a multielemental method for the analysis of major, minor and trace essential and toxic elements in milk. Several milk samples with different origins were collected from the Saudi Arabia markets and analyzed by Inductively Coupled Plasma Mass Spectrometer (ICP-MS). For preparation of the samples for analysis, they were digested by closed vessel microwave digestion system with H 2 O 2 /HNO 3 . About 40 elements were determined. A reference material was analysed for the validation of the proposed method. (Author)

The integrated performance evaluation program quality assurance guidance in support of EM environmental sampling and analysis activities

International Nuclear Information System (INIS)

1994-05-01

EM's (DOE's Environmental Restoration and Waste Management) Integrated Performance Evaluation Program (IPEP) has the purpose of integrating information from existing PE programs with expanded QA activities to develop information about the quality of radiological, mixed waste, and hazardous environmental sample analyses provided by all laboratories supporting EM programs. The guidance addresses the goals of identifying specific PE sample programs and contacts, identifying specific requirements for participation in DOE's internal and external (regulatory) programs, identifying key issues relating to application and interpretation of PE materials for EM headquarters and field office managers, and providing technical guidance covering PE materials for site-specific activities. (PE) Performance Evaluation materials or samples are necessary for the quality assurance/control programs covering environmental data collection

Ergonomic analysis of radiopharmaceuticals samples preparation process

International Nuclear Information System (INIS)

Gomes, Luciene Betzler C.; Santos, Isaac Luquetti dos; Fonseca, Antonio Carlos C. da; Pellini, Marcos Pinto; Rebelo, Ana Maria

2005-01-01

The doses of radioisotopes to be administrated in patients for diagnostic effect or therapy are prepared in the radiopharmacological sector. The preparation process adopts techniques that are aimed to reduce the exposition time of the professionals and the absorption of excessive doses for patients. The ergonomic analysis of this process contributes in the prevention of occupational illnesses and to prevent risks of accidents during the routines, providing welfare and security to the involved users and conferring to the process an adequate working standard. In this context it is perceived relevance of studies that deal with the analysis of factors that point with respect to the solution of problems and for establishing proposals that minimize risks in the exercise of the activities. Through a methodology that considers the application of the concepts of Ergonomics, it is searched the improvement of the effectiveness or the quality and reduction of the difficulties lived for the workers. The work prescribed, established through norms and procedures codified will be faced with the work effectively carried through, the real work, shaped to break the correct appreciation, with focus in the activities. This work has as objective to argue an ergonomic analysis of samples preparation process of radioisotopes in the Setor de Radiofarmacia do Hospital Universitario Clementino Fraga Filho da Universidade Federal do Rio de Janeiro (UFRJ). (author)

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)

Thin film analysis by instrumental heavy ion activation analysis using distributed recoil ranges of isotopic products

International Nuclear Information System (INIS)

Chowdhury, D.P.; Guin, R.; Saha, S.K.; Sudersanan, M.

2006-01-01

Thin foils (0.1 to 10 μm), metallic or polymeric, are frequently used in nuclear physics and chemistry experiments using ion beams from an accelerator. Very often it is important to know the major, minor and trace element composition of the foil. Several nuclear analytical techniques, namely RBS, ERDA, etc. are available for the near surface analysis. We have applied heavy ion activation analysis (HIAA) to explore the bulk composition of thin films. One of the difficulties in this method of thin film analysis is that the product nuclides from nuclear reaction come out of the sample surface due to high recoil energy. In thick sample, the recoiled nuclides are absorbed in the sample itself. This effect has been used to employ heavy ion activation for the analysis of thin films

Determination of Na, Cl, Ca, Mg, Mn and K in milk samples by activation analysis

International Nuclear Information System (INIS)

Kira, Carmen S.; Maihara, Vera A.

2000-01-01

In the present work cow milk samples distributed for Sao Paulo government institutions, by means of the 'Viva leite' programme, have been monitored. The concentrations of Ca, Cl, K, Mg, Mn and Na were determined in five milk samples and in three different kinds of commercial powder milk, by instrumental neutron activation. For quality control, the reference materials NIST whole milk powder and non fat milk powder were analysed. The results obtained are in the range of the concentrations mentioned in the literature for these elements. (author)

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)

A study of environmental analysis of urban river sediments using activation analysis

International Nuclear Information System (INIS)

Tanaka, Y.; Kuno, A.; Matsuo, M.

2003-01-01

Sediments of the Kitajukkengawa River (Sumida-ku, Tokyo, Japan) were analyzed by activation analyses. Concentrations of 36 elements for each sample were determined by instrumental neutron activation analysis (INAA) and neutron induced prompt gamma-ray analysis (PGA). Based on the correlation matrix between the elements in vertical distribution, principal component analysis (PCA) was performed. The degree of chemical weathering of silicate minerals was highest in the middle layer of the Kitajukkengawa River sediment and that adsorbed amount of trace metals such as Cd and Cr was increased along with chemical weathering. (author)

Transuranic waste characterization sampling and analysis plan

International Nuclear Information System (INIS)

1994-01-01

Los Alamos National Laboratory (the Laboratory) is located approximately 25 miles northwest of Santa Fe, New Mexico, situated on the Pajarito Plateau. Technical Area 54 (TA-54), one of the Laboratory's many technical areas, is a radioactive and hazardous waste management and disposal area located within the Laboratory's boundaries. The purpose of this transuranic waste characterization, sampling, and analysis plan (CSAP) is to provide a methodology for identifying, characterizing, and sampling approximately 25,000 containers of transuranic waste stored at Pads 1, 2, and 4, Dome 48, and the Fiberglass Reinforced Plywood Box Dome at TA-54, Area G, of the Laboratory. Transuranic waste currently stored at Area G was generated primarily from research and development activities, processing and recovery operations, and decontamination and decommissioning projects. This document was created to facilitate compliance with several regulatory requirements and program drivers that are relevant to waste management at the Laboratory, including concerns of the New Mexico Environment Department

Environmental sampling for trace analysis

International Nuclear Information System (INIS)

Markert, B.

1994-01-01

Often too little attention is given to the sampling before and after actual instrumental measurement. This leads to errors, despite increasingly sensitive analytical systems. This is one of the first books to pay proper attention to representative sampling. It offers an overview of the most common techniques used today for taking environmental samples. The techniques are clearly presented, yield accurate and reproducible results and can be used to sample -air - water - soil and sediments - plants and animals. A comprehensive handbook, this volume provides an excellent starting point for researchers in the rapidly expanding field of environmental analysis. (orig.)

Use of activation analysis of hair in environmental protection

International Nuclear Information System (INIS)

Obrusnik, I.

1982-01-01

Human hair is very suitable for use in environmental control monitoring because trace elements concentrate in it at higher levels than in most other organs. Unlike in other biological materials, the trace element contents in hair can be determined by instrumental neutron activation analysis (INAA), as the interference by 24 Na can be eliminated by appropriate washing of hair, e.g., using the procedure recommended by IAEA. The methods of sampling, washing and sample analysis using INAA and neutron activation analysis with radiochemical separation are described including the recommended way of the presentation of results. The results are presented of analyses for trace elements in hair from both little and highly polluted areas. (Ha)

Automated absolute activation analysis with californium-252 sources

International Nuclear Information System (INIS)

MacMurdo, K.W.; Bowman, W.W.

1978-09-01

A 100-mg 252 Cf neutron activation analysis facility is used routinely at the Savannah River Laboratory for multielement analysis of many solid and liquid samples. An absolute analysis technique converts counting data directly to elemental concentration without the use of classical comparative standards and flux monitors. With the totally automated pneumatic sample transfer system, cyclic irradiation-decay-count regimes can be pre-selected for up to 40 samples, and samples can be analyzed with the facility unattended. An automatic data control system starts and stops a high-resolution gamma-ray spectrometer and/or a delayed-neutron detector; the system also stores data and controls output modes. Gamma ray data are reduced by three main programs in the IBM 360/195 computer: the 4096-channel spectrum and pertinent experimental timing, counting, and sample data are stored on magnetic tape; the spectrum is then reduced to a list of significant photopeak energies, integrated areas, and their associated statistical errors; and the third program assigns gamma ray photopeaks to the appropriate neutron activation product(s) by comparing photopeak energies to tabulated gamma ray energies. Photopeak areas are then converted to elemental concentration by using experimental timing and sample data, calculated elemental neutron capture rates, absolute detector efficiencies, and absolute spectroscopic decay data. Calculational procedures have been developed so that fissile material can be analyzed by cyclic neutron activation and delayed-neutron counting procedures. These calculations are based on a 6 half-life group model of delayed neutron emission; calculations include corrections for delayed neutron interference from 17 O. Detection sensitivities of 239 Pu were demonstrated with 15-g samples at a throughput of up to 140 per day. Over 40 elements can be detected at the sub-ppM level

High priority tank sampling and analysis report

International Nuclear Information System (INIS)

Brown, T.M.

1998-01-01

In July 1993, the Defense Nuclear Facilities Board issued Recommendation 93-5 (Conway 1993) which noted that there was insufficient tank waste technical information and the pace to obtain it was too slow to ensure that Hanford Site wastes could be safely stored, that associated operations could be conducted safely, and that future disposal data requirements could be met. In response, the US Department of Energy, in May 1996, issued Revision 1 of the Recommendation 93-5 Implementation Plan (DOE-RL 1996). The Implementation Plan presented a modified approach to achieve the original plan's objectives, concentrating on actions necessary to ensure that wastes can be safely stored, that operations can be safely conducted, and that timely characterization information for the tank waste Disposal Program could be obtained. The Implementation Plan proposed 28 High Priority tanks for near term core sampling and analysis, which along with sampling and analysis of other non-High Priority tanks, could provide the scientific and technical data to confirm assumptions, calibrate models, and.measure safety related phenomenology of the waste. When the analysis results of the High Priority and other-tank sampling were reviewed, it was expected that a series of 12 questions, 9 related to safety issues and 3 related to planning for the disposal process, should be answered allowing key decisions to be made. This report discusses the execution of the Implementation Plan and the results achieved in addressing the questions. Through sampling and analysis, all nine safety related questions have been answered and extensive data for the three disposal planning related questions have been collected, allowing for key decision making. Many more tanks than the original 28 High Priority tanks identified in the Implementation Plan were sampled and analyzed. Twenty-one High Priority tanks and 85 other tanks were core sampled and used to address the questions. Thirty-eight additional tanks were auger

Novel Sample-handling Approach for XRD Analysis with Minimal Sample Preparation

Science.gov (United States)

Sarrazin, P.; Chipera, S.; Bish, D.; Blake, D.; Feldman, S.; Vaniman, D.; Bryson, C.

2004-01-01

Sample preparation and sample handling are among the most critical operations associated with X-ray diffraction (XRD) analysis. These operations require attention in a laboratory environment, but they become a major constraint in the deployment of XRD instruments for robotic planetary exploration. We are developing a novel sample handling system that dramatically relaxes the constraints on sample preparation by allowing characterization of coarse-grained material that would normally be impossible to analyze with conventional powder-XRD techniques.

GET electronics samples data analysis

International Nuclear Information System (INIS)

Giovinazzo, J.; Goigoux, T.; Anvar, S.; Baron, P.; Blank, B.; Delagnes, E.; Grinyer, G.F.; Pancin, J.; Pedroza, J.L.; Pibernat, J.; Pollacco, E.; Rebii, A.

2016-01-01

The General Electronics for TPCs (GET) has been developed to equip a generation of time projection chamber detectors for nuclear physics, and may also be used for a wider range of detector types. The goal of this paper is to propose first analysis procedures to be applied on raw data samples from the GET system, in order to correct for systematic effects observed on test measurements. We also present a method to estimate the response function of the GET system channels. The response function is required in analysis where the input signal needs to be reconstructed, in terms of time distribution, from the registered output samples.

Quartz analysis in gravimetric sampling

International Nuclear Information System (INIS)

Rex, D.A.

1990-01-01

An overview of the methods employed in the assessment of quartz exposure is provided. The principles and some of the problems associated with each method is discussed. The methods reviewed include wet chemical methods, X-ray diffraction and infrared absorption of which the latter two methods are deemed appropriate for analysing quartz on personal gravimetric collected samples. The implications of combining area samples collected over a six month period, and performing only a single quartz analysis rather than separate analyses, are considered. Finally, various options open to mines with regard to their involvement with quartz analysis are also briefly discussed. 35 refs., 6 figs., 1 tab

Urine sample preparation for proteomic analysis.

Science.gov (United States)

Olszowy, Pawel; Buszewski, Boguslaw

2014-10-01

Sample preparation for both environmental and more importantly biological matrices is a bottleneck of all kinds of analytical processes. In the case of proteomic analysis this element is even more important due to the amount of cross-reactions that should be taken into consideration. The incorporation of new post-translational modifications, protein hydrolysis, or even its degradation is possible as side effects of proteins sample processing. If protocols are evaluated appropriately, then identification of such proteins does not bring difficulties. However, if structural changes are provided without sufficient attention then protein sequence coverage will be reduced or even identification of such proteins could be impossible. This review summarizes obstacles and achievements in protein sample preparation of urine for proteome analysis using different tools for mass spectrometry analysis. The main aim is to present comprehensively the idea of urine application as a valuable matrix. This article is dedicated to sample preparation and application of urine mainly in novel cancer biomarkers discovery. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Quantitative analysis of untreated bio-samples

International Nuclear Information System (INIS)

Sera, K.; Futatsugawa, S.; Matsuda, K.

1999-01-01

A standard-free method of quantitative analysis for untreated samples has been developed. For hair samples, measurements were performed by irradiating with a proton beam a few hairs as they are, and quantitative analysis was carried out by means of a standard-free method developed by ourselves. First, quantitative values of concentration of zinc were derived, then concentration of other elements was obtained by regarding zinc as an internal standard. As the result, values of concentration of sulphur for 40 samples agree well with the average value for a typical Japanese and also with each other within 20%, and validity of the present method could be confirmed. Accuracy was confirmed by comparing the results with those obtained by the usual internal standard method, too. For the purpose of a surface analysis of a bone sample, a very small incidence angle of the proton beam was used, so that both energy loss of the projectile and self-absorption of X-rays become negligible. As the result, consistent values of concentration for many elements were obtained by the standard-free method

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

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)

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

Energy Technology Data Exchange (ETDEWEB)

Armelin, Maria Jose Aguirre

1978-07-01

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

Determination of toxic and trace elements in human hair and sediment samples by reactor neutron activation analysis technique based-on the k-zero method

International Nuclear Information System (INIS)

Ho Manh Dung; Nguyen Mong Sinh; Nguyen Thanh Binh; Cao Dong Vu; Nguyen Thi Si

2004-01-01

The analysis of human hair can evaluate the degree of environmental pollutants exposure to human body, intakes of food and metabolism. Also, the analysis of sediment can aid in reconstructing the history of changes, understanding human impact on the ecosystem, and suggesting possible remedial strategies. The k o -standardization method of neutron activation analysis (k o -NAA) on research reactor is capable to play an important role as a main analytical technique with the advantages of sensitivity, precision, accuracy, multielement and routine for the sample object. Therefore, the project's aim is to build the k o -NAA procedures on the Dalat research reactor for the analysis of human hair and sediment samples. The K o -NAA procedure on the Dalat research reactor is able to determine of multielement: Ag, Al, As, Br, Ca, Cl, Co, Cr, Cu, Fe, Hg, I, K Mg, Mn, Na, S, Sb, Se, Sr, Ti, V and Zn in The human hair; and of multielement: As, Co, Cr, Cs, Fe, Hf, K, La, Mn, Na Rb, Sb, Sc, Yb and Zn in the sediment. (author)

An approach to the selection of recommended cooling intervals for the activation analysis of unknown samples with Ge(Li) gamma-ray spectrometry

International Nuclear Information System (INIS)

Hirose, Akio; Ishii, Daido

1975-01-01

Estimation of the optimum cooling interval by the mathematic or graphic method for Ge(Li) γ-ray spectrometry performed in the presence of some Compton interferences, and the recommended cooling intervals available for activation analysis of unknown samples have been proposed, and applied to the non-destructive activation analysis of gold in pure copper. In the presence of Compton interferences, two kinds of optimum cooling intervals were discussed. One maximizes the S/N ratio of a desired photo-peak. This interval had been originated by Isenhour, et al. Using the computer technique, this work is abbreviated as tsub( s/ n). The other, which minimizes the relative standard deviation (delta s/S) of a net photo-peak counting rate of interest (S) was originated by Tomov, et al. and Quittner, et al., this work is abbreviated as tsub(opt) or t'sub(opt). All equations derived by the above authors, however, have the practical disadvantage of including a term relating to the intensity of the desired photo-peak, thus making it difficult to predict the optimum cooling interval before irradiation. Since in chemical analysis, the concentration of the desired element, or the intensity of the photo-peak of interest, should be considered as ''unknown''. In the present work, an approach to the selection of recommended cooling interval applicable to the unknown sample has been discussed, and the interval, tsub(opt), which minimizes the lower limit of detection of a desired element under given irradiation and counting conditions has been proposed. (Evans, J.)

UMTRA project water sampling and analysis plan -- Shiprock, New Mexico

International Nuclear Information System (INIS)

1994-02-01

Water sampling and analysis plan (WSAP) is required for each U.S. Department of Energy (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site to provide a basis for ground water and surface water sampling at disposal and former processing sites. This WSAP identifies and justifies the sampling locations, analytical parameters, detection limits, and sampling frequency for the monitoring stations at the Navaho Reservation in Shiprock, New Mexico, UMTRA Project site. The purposes of the water sampling at Shiprock for fiscal year (FY) 1994 are to (1) collect water quality data at new monitoring locations in order to build a defensible statistical data base, (2) monitor plume movement on the terrace and floodplain, and (3) monitor the impact of alluvial ground water discharge into the San Juan River. The third activity is important because the community of Shiprock withdraws water from the San Juan River directly across from the contaminated alluvial floodplain below the abandoned uranium mill tailings processing site

Limits of detection in instrumental neutron activation analysis

International Nuclear Information System (INIS)

Guinn, V.P.

1990-01-01

Lower limits of detection (LLODs), frequently referred to simply as limits of detection and abbreviated as LODs, often appear in the literature of analytical chemistry - for numerous different methods of elemental and/or molecular analysis. In this chapter, one particular method of quantitative elemental analysis, that of instrumental neutron activation analysis (INAA), is the subject discussed, with reference to LODs. Particularly in the literature of neutron activation analysis (NAA), many tables of 'interference-free' NAA LODs are available. Not all of these are of much use, because (1) for many the definition used for LOD is not clear, or reasonable, (2) for many, the analysis conditions used are not clearly specified, and (3) for many, the analysis conditions used are specified, but not very practicable for most laboratories. For NAA work, such tables of interference-free LODs are, in any case, only applicable to samples in which, at the time of counting, only one radionuclide is present to any significant extent in the activated sample. It is important to note that tables of INAA LODs, per se, do not exist - since the LOD for a given element, under stated analysis conditions, can vary by orders of magnitude, depending on the elemental composition of the matrix in which it is present. For any given element, its INAA LOD will always be as large as, and usually much larger than, its tabulated 'interference-free' NAA LOD - how much larger depending upon the elemental composition of the matrix in which it is present. As discussed in this chapter, however, an INAA computer program exists that can calculate realistic INAA LODs for any elements of interest, in any kind of specified sample matrix, under any given set of analysis conditions

Elemental and isotopic characterization of Japanese and Philippine polished rice samples using instrumental neutron activation analysis and isotope ratio mass spectrometry

International Nuclear Information System (INIS)

Pabroa, Preciosa Corazon B.; Sucgang, Raymond J.; Mendoza, Norman dS.; Ebihara, Mitsuru

2011-01-01

Rice is a staple food for most Asian countries such as the Philippines and Japan and as such its elemental and isotopic content are of interest to the consumers. Its elemental content may reflect the macro nutrient reduction during milling or probable toxic elements uptake. Three Japanese and four Philippine polished rice samples in his study mostly came from rice bought from supermarkets.These rice samples were washed, dried and ground to fine powder. Instrumental neutron activation analysis (INAA), a very sensitive non-destructive multi-element analytical technique, was used for the elemental analysis of the samples and isotope-ratio mass spectrometry (IRMS) was used to obtain the isotopic signatures of the samples. Results show that compared with the unpolished rice standard NIES CRM10b, the polished Japanese and Philippine rice sampled show reduced concentrations of elements by as much as 1/3 to 1/10 of Mg, Mn, K and Na. Levels of Ca and Zn are not greatly affected. Arsenic is found in all the Japanese rice tested at an average concentration of 0.103 μg/g and three out of four of the Philippine rice at an average concentration of 0.070 μg/g. Arsenic contamination may have been introduced from the fertilizer used in rice fields. Higher levels of Br are seen in two of the Philippine rice at 14 and 34 μg/g with the most probable source being the pesticide methyl bromide. Isotopic ratio of ae 13 C show signature of a C3 plant with possible narrow distinguishable signature of Japanese rice within -27.5 to -28.5 while Philippine rice within -29 to -30. More rice samples will be analyzed to gain better understanding of isotopic signatures to distinguish inter-varietal and/or geographical differences. Elemental composition of soil samples of rice samples sources will be determined for better understanding of uptake mechanisms. (author)

Non-destructive alpha-particle activation analysis of P, Cl, K and Ca in marine macro-alga samples using synthetic multielement reference material as comparative standard

International Nuclear Information System (INIS)

Iwata, Y.; Naitoh, H.; Suzuki, N.

1992-01-01

A Synthetic Reference Material (SyRM) composed with accurately known amounts of 12 elements has been prepared. The elemental composition of the SyRM is closely similar to that of marine macro-algae sample. The elemental composition of the SyRM was regulated by the starting materials used for the synthesis. The SyRM was used as a comparative standard for non-destructive alpha-particle activation analysis of marine macro-alga samples. P, Cl, K and Ca were determined simultaneously without correction for alpha range due to difference in the elemental composition between the analytical samples and the comparative standard. (author) 19 refs.; 4 tabs

Depth Distribution Studies of Carbon in Steel Surfaces by Means of Charged Particle Activation Analysis with an Account of Heat and Diffusion Effects in the Sample

Energy Technology Data Exchange (ETDEWEB)

Brune, D; Lorenzen, J [AB Atomenergi, Nykoeping (Sweden); Witalis, E [Swedish National Defence Research Inst., Stockholm (Sweden)

1972-05-15

Depth distribution studies of carbon in steel and iron were carried out in the concentration range 0.05-1 %, using proton activation analysis. Surface content studies were performed in the concentration range 0.01-1 % using deuteron activation analysis. The following reactions were utilized: {sup 12}C(p,{gamma}){sup 13}N and {sup 12}C(d,n){sup 13}N Evaluations of depth distribution were based on resonances in the excitation function. The carbon content was determined with the aid of the positron emitter, {sup 13}N, using either single-peak or coincidence measurements. The heat dissipation in the irradiated region of the samples was calculated, and the temperature rise was measured using thermocouples. The temperature distribution within the hot zone subjected to irradiation by charged particles, together with the temperature distribution around this zone, was studied in order to estimate any effect this might have on the carbon diffusion. A device for automatic sample exchange which is remotely controlled is described.

Depth Distribution Studies of Carbon in Steel Surfaces by Means of Charged Particle Activation Analysis with an Account of Heat and Diffusion Effects in the Sample

International Nuclear Information System (INIS)

Brune, D.; Lorenzen, J.; Witalis, E.

1972-05-01

Depth distribution studies of carbon in steel and iron were carried out in the concentration range 0.05-1 %, using proton activation analysis. Surface content studies were performed in the concentration range 0.01-1 % using deuteron activation analysis. The following reactions were utilized: 12 C(p,γ) 13 N and 12 C(d,n) 13 N Evaluations of depth distribution were based on resonances in the excitation function. The carbon content was determined with the aid of the positron emitter, 13 N, using either single-peak or coincidence measurements. The heat dissipation in the irradiated region of the samples was calculated, and the temperature rise was measured using thermocouples. The temperature distribution within the hot zone subjected to irradiation by charged particles, together with the temperature distribution around this zone, was studied in order to estimate any effect this might have on the carbon diffusion. A device for automatic sample exchange which is remotely controlled is described

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

Determination of short half-life elements in biological, foodstuff, and environmental samples qualitatively by neutron activation analysis

International Nuclear Information System (INIS)

Syukria Kurniawati; Muhayatun Santoso; Diah Dwiana Lestiani

2010-01-01

NAA applications at routine operation power of 15 MW at Multipurpose Reactor GA Siwabessy (MPR-GAS) for sample matrices analysis have been widely applied. However, the results are not optimum for some matrices especially for short half-live elements. Preliminary study of short half-life elements determination in biological, foodstuff, and environmental samples using 1 MW power have been conducted to solve this problem. The samples were irradiated in rabbit system of MPR-GAS for 5 minutes, counted for 200 seconds by HPGe detector, and the spectrum were analyzed further using software Genie 2000 and Bandung NAA Utility. Analysis under 1 MW power on biological and foodstuff samples were capable to detect eight elements: Al, Br, CI, Ca, I, K, Mg, Ti, and Na for biological samples; Al, Br, CI, Ca, I, K, Mg, Mn, and Na for foodstuff samples, while at 15 MW power only three elements (CI, K, Na) were detected. At 1 MW power the counting process is more optimum due to smaller radiation exposure and dead time. For the environmental samples, the number of elements detected by 1 MW and 15 MW powers did not differ significantly. Generally, the results on the three types of samples showed that the elements of short half-life are better detected at 1 MW than that of 15 MW power. Further research needs to be done to obtain the optimum analytical conditions for irradiation and counting time determination. (author)

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.)

Activation analysis of some seaweeds of Myanmar

Energy Technology Data Exchange (ETDEWEB)

Myint, U; Myint, Aye Myint [Yangon Univ. (Myanmar). Dept. of Chemistry

1994-11-01

Activation analysis of some seaweed samples occurring off the coastline areas of Myanmar is described. Na, K and I were determined using Am(Be) radionuclide neutron source and low level [beta]-counting. (author) 3 refs.; 1 fig.; 2 tabs.

Sampling quality assurance guidance in support of EM environmental sampling and analysis activities

International Nuclear Information System (INIS)

1994-05-01

This document introduces quality assurance guidance pertaining to the design and implementation of sampling procedures and processes for collecting environmental data for DOE's Office of EM (Environmental Restoration and Waste Management)

Soil sampling and analysis plan for the 3718-F Alkali Metal Treatment and Storage Facility closure activities

Energy Technology Data Exchange (ETDEWEB)

Sonnichsen, J.C.

1997-05-01

Amendment V.13.B.b to the approved closure plan (DOE-RL 1995a) requires that a soil sampling and analysis plan be prepared and submitted to the Washington State Department of Ecology (Ecology) for review and approval. Amendment V.13.B.c requires that a diagram of the 3718-F Alkali Metal Treatment and Storage Facility unit (the treatment, storage, and disposal [TSD] unit) boundary that is to be closed, including the maximum extent of operation, be prepared and submitted as part is of the soil sampling and analysis plan. This document describes the sampling and analysis that is to be performed in response to these requirements and amends the closure plan. Specifically, this document supersedes Section 6.2, lines 43--46, and Section 7.3.6 of the closure plan. Results from the analysis will be compared to cleanup levels identified in the closure plan. These cleanup levels will be established using residential exposure assumptions in accordance with the Model Toxics Control Act (MTCA) Cleanup Regulation (Washington Administrative Code [WAC] 173-340) as required in Amendment V.13.B.I. Results of all sampling, including the raw analytical data, a summary of analytical results, a data validation package, and a narrative summary with conclusions will be provided to Ecology as specified in Amendment V.13.B.e. The results and process used to collect and analyze the soil samples will be certified by a licensed professional engineer. These results and a certificate of closure for the balance of the TSD unit, as outlined in Chapter 7.0 of the approved closure plan (storage shed, concrete pad, burn building, scrubber, and reaction tanks), will provide the basis for a closure determination.

Soil sampling and analysis plan for the 3718-F Alkali Metal Treatment and Storage Facility closure activities

International Nuclear Information System (INIS)

Sonnichsen, J.C.

1997-01-01

Amendment V.13.B.b to the approved closure plan (DOE-RL 1995a) requires that a soil sampling and analysis plan be prepared and submitted to the Washington State Department of Ecology (Ecology) for review and approval. Amendment V.13.B.c requires that a diagram of the 3718-F Alkali Metal Treatment and Storage Facility unit (the treatment, storage, and disposal [TSD] unit) boundary that is to be closed, including the maximum extent of operation, be prepared and submitted as part is of the soil sampling and analysis plan. This document describes the sampling and analysis that is to be performed in response to these requirements and amends the closure plan. Specifically, this document supersedes Section 6.2, lines 43--46, and Section 7.3.6 of the closure plan. Results from the analysis will be compared to cleanup levels identified in the closure plan. These cleanup levels will be established using residential exposure assumptions in accordance with the Model Toxics Control Act (MTCA) Cleanup Regulation (Washington Administrative Code [WAC] 173-340) as required in Amendment V.13.B.I. Results of all sampling, including the raw analytical data, a summary of analytical results, a data validation package, and a narrative summary with conclusions will be provided to Ecology as specified in Amendment V.13.B.e. The results and process used to collect and analyze the soil samples will be certified by a licensed professional engineer. These results and a certificate of closure for the balance of the TSD unit, as outlined in Chapter 7.0 of the approved closure plan (storage shed, concrete pad, burn building, scrubber, and reaction tanks), will provide the basis for a closure determination

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

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

International Nuclear Information System (INIS)

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

2004-01-01

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

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.

Epithermal neutron activation analysis for studying the environment

International Nuclear Information System (INIS)

Frontas'eva, M.V.; Steinnes, E.

1997-01-01

Epithermal neutron activation analysis (ENAA) has certain advantages over the conventional instrumental analysis (INAA) in terms of improvement in precision and lowering of detection limits, reduction of high matrix activity and fission interferences if any. The current status and the applications of ENAA to environmental samples are reviewed. Experience in the use of ENAA in the monitoring of atmospheric depositions by means of moss-biomonitors at pulsed fast reactor IBR-2 in Dubna is summarized. INAA has shown to be useful for a number of sample types of interest in environmental studies, and should find more extensive use in this area. Analysis of airborne particulate matter is a case where ENAA should be particularly useful. A similar case where ENAA has shown strong performance is in the analysis of mosses used as biomonitors of atmospheric deposition, where 45 elements were determined. In this and other cases, however, induction-coupled plasma mass spectrometry is a very strong competitor, offering data for even more elements. A comparison of ENAA and ICP-MS for moss analysis is presented, and cases where ENAA is unique are discussed

Preparation of hair and nail samples for trace element analysis

International Nuclear Information System (INIS)

Scoble, H.A.; Litman, R.

1978-01-01

The method of washing of human hair and nail samples is examined by neutron activation and γ-ray analysis. The amounts of Na, K, Br, Au, Zn, and La that are removed by successive washings determine the optimum number of washing for removing these trace elements as surface contaminants. A total solution contact time with the nails is 5 minutes, and leaching effcts are observed after 6 washings

Methods of charged-particle activation analysis

International Nuclear Information System (INIS)

Chaudhri, M. Anwar; Chaudhri, M. Nasir; Jabbar, Q.; Nadeem, Q.

2006-01-01

The accuracy of Chaudhri's method for charged-particle activation analysis published in J. Radioanal. Chem. (1977) v. 37 p. 243 has been further demonstrated by extensive calculations. The nuclear reactions 12 C(d,n) 13 N, 63 Cu( 3 He,p) 65 Zn, 107 Ag(α,n) 110 In and 208 Pb(d,p) 209 Pb, the cross sections of which were easily available, have been examined for the detection of 12 C, 63 Cu, 107 Ag and 208 Pb, respectively, in matrices of Cu, Zr and Pb, at the bombarding energies of 4 - 22 MeV. The 'standard' is assumed to be in a carbon matrix. It has been clearly demonstrated that Chaudhri's method, which makes the charged particle activation analysis as simple as neutron activation analysis, provides results which are almost identical to, or only about 1-2 % different, from the results obtained using the full 'Activity Equation' involving solving complex integrals. It is valid even when the difference in the average atomic weights of matrices of the standard and the sample is large. (author)

Microbiological Analysis of an Active Pilot-Scale Mobile Bioreactor Treating Organic Contaminants

International Nuclear Information System (INIS)

Brigmon, R.L.

1997-01-01

Samples were obtained for microbiological analysis from a granular activated carbon fluidized bed bioreactor (GAC-FBR). This GAC-FBR was in operation at a former manufactured gas plant (MGP) Site in Augusta Georgia for in situ groundwater bioremediation of organics. The samples included contaminated site groundwater, GAC-FBR effluent, and biofilm coated granular activated carbon at 5, 9, and 13 feet within the GAC-FBR column. The objective of this analysis was to correlate contaminant removal with microbiological activity within the GAC-FBR

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

Modern trends in activation analysis. Vols. 1 and 2

Energy Technology Data Exchange (ETDEWEB)

Henkelmann, R; Kim, J I; Lux, F; Staerk, H; Zeisler, R [eds.

1976-01-01

Two volumes contain 164 special papers presented at the international conference on activation analysis, including five plenary lectures which give a general survey of modern trends and possibilities of applications in fields where activation analysis is capable of solving problems which are hitherto unsolved. The emphasis during this meeting is put on applications, though other subjects (e.g. sampling, homogeneity of samples, instrumental development, computer evaluation of gamma spectra, comparisons with other analytical methods) are also dealt with. The proceedings contain lectures on applications in the fields of biology, biomedicine, archaeology, the arts, forensic sciences, environmental research, ecology, materials research, geo- and cosmo-sciences, and other individual applications.

Activity Concentration for Surface Soil Samples Collected from Arrant, Qena, Egypt

International Nuclear Information System (INIS)

Harb, S.; Salahel Din, K.; Abbady, A.; Moustafa, M.

2010-01-01

Soil samples were collected from four regions from Armant area. Qena, Upper Egypt for measure their natural radioactivity concentrations due to Ra-226, Th-232 and K-40 radionuclides. Thirty-Four surface soil samples were analyzed by using low-level gamma-spectrometric analysis. The average activity concentration for Ra-226 in (Bq/kg) in the collected soil samples were found to be 27.3 ±3.2, 11.4±1.09, 10.6±1.2, and 11.4±1.02 while the average value for Th-232 were 15.1±1.4, 11.1±0.77, 10.8 ± 0.72 and 11.1 ± 0.8 (Bq/kg) for soil samples from North, South, West and East. The corresponding average values for K-40 were 521.4±16.8, 463±14.8, 488.9±15.6 and 344.5±10.7 (Bq/kg), respectively. Based on radionuclides concentration in surface soil samples the radiological effects can be assessed

Large scale sample management and data analysis via MIRACLE

DEFF Research Database (Denmark)

Block, Ines; List, Markus; Pedersen, Marlene Lemvig

Reverse-phase protein arrays (RPPAs) allow sensitive quantification of relative protein abundance in thousands of samples in parallel. In the past years the technology advanced based on improved methods and protocols concerning sample preparation and printing, antibody selection, optimization...... of staining conditions and mode of signal analysis. However, the sample management and data analysis still poses challenges because of the high number of samples, sample dilutions, customized array patterns, and various programs necessary for array construction and data processing. We developed...... a comprehensive and user-friendly web application called MIRACLE (MIcroarray R-based Analysis of Complex Lysate Experiments), which bridges the gap between sample management and array analysis by conveniently keeping track of the sample information from lysate preparation, through array construction and signal...