Correcting the effects of the matrix using capture gamma-ray spectrometry: Application to measurement by Active Neutron Interrogation

International Nuclear Information System (INIS)

Baudry, G.

2003-11-01

In the field of the measurement of low masses of fissile material ( 235 U, 239 Pu, 241 Pu) in radioactive waste drums, the Active Neutron Interrogation is a non-destructive method achieving good results. It does however remain reliant upon uncertainties related to the matrix effects on interrogation and fission neutrons. The aim of this thesis is to develop a correction method able to take into account these matrix effects by quantifying the amount of absorbent materials (chlorine and hydrogen) in a 118- liter homogeneous matrix. The main idea is to use the gamma-ray spectrometry of gamma emitted by neutron captures to identify and quantify the composition of the matrix. An indicator from its chlorine content is then deduced in order to choose the calibration coefficient which best represents the real composition of the matrix. This document firstly presents the needs of control and characterization of radioactive objects, and the means used in the field of nuclear measurement. Emphases is put in particular on the Active Neutron Interrogation method. The matrices of interest are those made of light technological waste (density ≤ 0,4 g/cm 3 ) containing hydrogenated and chlorinated materials. The advantages of gamma-rays emitted by neutron captures for the determination of a chlorine content indicator of the matrices and the principles of the correction method are then explained. Measurements have been firstly realized with an existing Neutron Interrogation device (PROMETHEE 6). Such measurements have proven its inadequacy: no signal from the matrix hydrogen was detected, due to an intense signal from the polyethylene contained in some cell elements. Moreover, the matrix chlorine content appeared difficult to be measured. A new and specific device, named REGAIN and dedicated to active gamma-rays spectrometry, was defined with the Monte-Carlo N-Particle (MCNP) code. The experiments conducted with this new device made it possible to detect the hydrogen from the

Handbook on Mobile Gamma-ray Spectrometry

DEFF Research Database (Denmark)

Aage, Helle Karina; Korsbech, Uffe C C

2003-01-01

Basic physics and mathematics for Airborne and Car-borne Gamma-ray Spectrometry supplemented with practical examples and methods for advanced data processing......Basic physics and mathematics for Airborne and Car-borne Gamma-ray Spectrometry supplemented with practical examples and methods for advanced data processing...

Advances in continuous gamma-ray spectrometry and applications

International Nuclear Information System (INIS)

Gold, R.; McNeece, J.P.; Kaiser, B.J.

1984-07-01

Recent advances and applications in continuous Compton recoil gamma-ray spectrometry are described. Applications of continuous gamma-ray spectrometry are presented for: (1) Characterization of light water reactor (LWR) pressures vessel (PV) environments. (2) Assessment of fuel distributions for Three Mile Island Unit 2 (TMI-2) reactor recovery. (3) Measurement of LWR-PV-neutron exposure. The latest improvements attained with the Janus probe, a special in-situ configuration of Si(Li) detectors, are presented. The status of current efforts to extend the domain of applicability of this method beyond 3 MeV is discussed with emphasis on recent work carried out with Si(Li) detectors of much larger volume

Guidelines for radioelement mapping using gamma ray spectrometry data

International Nuclear Information System (INIS)

2003-07-01

The purpose of the report is to provide an up-to-date review on the use of gamma ray spectrometry for radioelement mapping and, where appropriate, provide guidelines on the correct application of the method. It is a useful training guide for those new to the method. It gives a broad coverage of all aspects of the gamma ray method and provides a comprehensive list of references. The report gives an overview of the theoretical background to radioactivity and the gamma ray spectrometric method followed by a review of the application of the method to mapping the radiation environment. A brief outline is presented of the principles of radioactivity, the interaction of gamma rays with matter, instrumentation applied to the measurement of gamma rays, and the quantities and units in contemporary use in gamma ray spectrometry. This is followed by a review of the fundamentals of gamma ray spectrometry, and its application to ground and airborne mapping. Covered are also all aspects of the calibration and data processing procedures required for estimating the ground concentrations of the radioelements. The procedures required for the recovery of older survey data are also presented as well as an overview of data presentation and integration for mapping applications

Fast-ion energy resolution by one-step reaction gamma-ray spectrometry

DEFF Research Database (Denmark)

Salewski, Mirko; Nocente, M.; Gorini, G.

2016-01-01

The spectral broadening of γ-rays from fusion plasmas can be measured in high-resolution gamma-ray spectrometry (GRS). We derive weight functions that determine the observable velocity space and quantify the velocity-space sensitivity of one-step reaction high-resolution GRS measurements in magne...

Use of X-Ray Fluorescence Spectrometry to Determine Trace ...

African Journals Online (AJOL)

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

Comparison of in-situ gamma ray spectrometry measurements with conventional methods in determination natural and artificial nuclides in soil

International Nuclear Information System (INIS)

Al-Masri, M. S.; Doubal, A. W.

2010-12-01

Two nuclear analytical techniques (In-Situ Gamma ray spectrometry and laboratory gamma ray spectrometry) for determination of natural and artificial radionuclides in soil have been validated. The first technique depends on determination of radioactivity content of representative samples of the studied soil after laboratory preparation, while the second technique is based on direct determination of radioactivity content of soil using in-situ gamma-ray spectrometer. Analytical validation parameter such as detection limits, repeatability, reproducibility in addition to measurement uncertainties were estimated and compared for both techniques. Comparison results have shown that the determination of radioactivity in soil should apply the two techniques together where each of techniques is characterized by its low detection limit and uncertainty suitable for defined application of measurement. Radioactive isotopes in various locations were determined using the two methods by measuring 40 k, 238 U,and 137 Cs. The results showed that there are differences in attenuation factors due to soil moisture content differences; wet weight corrections should be applied when the two techniques are compared. (author)

Detector calibration for in-situ gamma ray spectrometry

CERN Document Server

Balea, G

2002-01-01

The power in the technique of in-situ spectrometry lies in the fact that a detector placed on ground measures gamma radiation from sources situated over an area of several hundred square meters. The 'field of view' for the detector would be larger for high energy radiation sources and for sources closer to the soil surface. In contrast, a soil sample would represent an area of a few tens of hundreds of square centimeters. In practice, an effective characterization of a site would involve in-situ gamma ray spectrometry in conjunction with soil sampling. As part of an overall program, in-situ gamma ray spectrometry provides a means to assess the degree of contamination in areas during the course of operations in the field, thus guiding the investigator on where to collect samples. It can also substantially reduce the number of samples need to be collected and subsequently analyzed. (author)

Improvements on Low Level Activity Gamma Measurements and X-ray Spectrometry at the CEA-MADERE Measurement Platform

Directory of Open Access Journals (Sweden)

Sergeyeva Victoria

2016-01-01

Full Text Available The CEA MADERE platform (Measurement Applied to DosimEtry in REactors is a part of the Instrumentation Sensors and Dosimetry Laboratory (LDCI. This facility is dedicated to the specific activity measurements of solid and radioactive samples using Gamma and X-ray spectrometry. MADERE is a high-performance facility devoted to neutron dosimetry for experimental programs performed in CEA and for the irradiation surveillance programmes of PWR vessels. The MADERE platform is engaged in a continuous improvement process. Recently, two High Efficiency diodes have been integrated to the MADERE platform in order to manage the accurate low level activity measurements (few Bq per sample. This new equipment provides a good level of efficiency over the energy range from 60 keV to 2 MeV. The background continuum is reduced due to the use of a Ultra Low Background (ULB lead shielding. Relative and absolute X-ray measurement techniques have been improved in order to facilitate absolute rhodium activity measurement (Rh103m on solid samples. Additional efforts have been made to increase the accuracy of the relative niobium (Nb93m activity measurement technique. The way of setting up an absolute measurement method for niobium is under investigation. After a presentation of the MADERE's measurement devices, this paper focuses on the technological options taken into account for the design of high efficiency measurement devices. Then, studies performed on X-ray measurement techniques are presented. Some details about the calculation of uncertainties and correction factors are also mentioned. Finally, future research and development axes are exposed.

Prompt gamma-ray spectrometry for measurement of B-10 concentration in brain tissue and blood

International Nuclear Information System (INIS)

Nakagawa, Yoshinobu; Kitamura, Katsuji; Kobayashi, Toru; Matsumoto, Keizo; Hatanaka, Hiroshi.

1993-01-01

Boron-10 (B-10) concentration in the brain tissue and blood was measured continuously for 24 hours after injection of the B-10 compound in live rabbits using prompt gamma-ray spectrometry. Following injection of B-10 compound (Na 2 B 12 H 11 SH, 50mg/kg) dissolved in physiological saline, B-10 concentration was continuously measured in the brain tissue. Intermittently the concentration of B-10 in blood and cerebro-spinal fluid (CSF) was also measured. In 10 minutes after the injection of B-10 compound, the level of B-10 concentration reached the peak of 400-500 ppm in blood and 20-30 ppm in the normal brain tissue. In 60 minutes the level of B-10 concentration rapidly decreased and then a gradual decline was observed. The value was 15-30 ppm at 3 hours after injection, 5-10 ppm at 6 hours and 2-5 ppm at 24 hours in the blood. The concentration in the brain tissue was 3-8 ppm at 3 hours, 2-5 ppm at 6 hours and below 1.5 ppm at 24 hours. B-10 concentration in cerebro-spinal fluid was below 1 ppm. B-10 concentration was also measured in the brain tumor and blood in the human cases at boron neutron capture therapy (BNCT). These data studied by prompt gamma-ray spectrometry are very important and useful to decide the irradiation time. (author)

Measurement of ²²⁶Ra in soil from oil field: advantages of γ-ray spectrometry and application to the IAEA-448 CRM.

Science.gov (United States)

Ceccatelli, A; Katona, R; Kis-Benedek, G; Pitois, A

2014-05-01

The analytical performance of gamma-ray spectrometry for the measurement of (226)Ra in TENORM (Technically Enhanced Naturally Occurring Radioactive Material) soil was investigated by the IAEA. Fast results were obtained for characterization and certification of a new TENORM Certified Reference Material (CRM), identified as IAEA-448 (soil from oil field). The combined standard uncertainty of the gamma-ray spectrometry results is of the order of 2-3% for massic activity measurement values ranging from 16500 Bq kg(-1) to 21500 Bq kg(-1). Methodologies used for the production and certification of the IAEA-448 CRM are presented. Analytical results were confirmed by alpha spectrometry. The "t" test showed agreement between alpha and gamma results at 95% confidence level. © 2013 Published by Elsevier Ltd.

The participation of ATOMKI in the G-2 international intercomparison of high precision gamma-ray spectrometry measurements

International Nuclear Information System (INIS)

Gaspar, A.; Lakatos, T.; Sulik, B.; Toeroek, I.

1981-01-01

International intercomparison had been organized by the IAEA in high precision gamma spectrometry. Five mixed-spectrum sources were prepared and sent to the participants by the IAEA for relative gamma emission rate measurements. This source type enables the whole measuring method and procedure to be tested. Measurements were carried out using two independent methods: a.) simple normalization to an additional radioactive source; b.) using a time variant pulse processor and random pulse generator for correction of dead-time and pile-up losses. The results agreed in most cases within +-1% with the IAEA results. (R.J.)

Decreasing of the detection limit for gamma-ray Spectrometry with the influence of sample treatment

International Nuclear Information System (INIS)

Karami, M.; Sadighzadeh, A.; Asgharizadeh, F.; Sardari, D.; Tavassoli, A.; Arbabi, A.; Hochaghani, O.

2009-01-01

Full text: In this study the ash method has been applied for environmental sample treatment in order to decrease of the detection limit in gamma-ray spectrometry for low level radioactivity measurements. Detection limit in gamma ray spectrometry is the smallest expectation value of the net counting rate that can be detected on given probabilities. The environmental test samples have been changed into ash using a suitable oven. The heating were made under controlled temperature to avoid the escape of some radionuclides such as radiocaesium. The ash samples were measured by high resolution gamma-ray spectrometry system. (author)

Applied gamma-ray spectrometry

CERN Document Server

Dams, R; Crouthamel, Carl E

1970-01-01

Applied Gamma-Ray Spectrometry covers real life application of the gamma-ray and the devices used in their experimental studies. This book is organized into 9 chapters, and starts with discussions of the various decay processes, the possible interaction mechanisms of gamma radiation with matter, and the intrinsic and extrinsic variables, which affect the observed gamma-ray and X-ray spectra. The subsequent chapters deal with the properties and fabrication of scintillation detectors, semiconductor detectors, and proportional gas counters. These chapters present some of the most widely utilized

On response operator in semiconductor gamma ray spectrometry

Energy Technology Data Exchange (ETDEWEB)

Krnac, S [Slovak Technical Univ., Bratislava (Slovakia); Povinec, P [International Atomic Energy Agency, Monaco (Monaco). MEL; Ragan, R [Inst. of Preventive and Clinical Medicine, Bratislava (Slovakia)

1996-12-31

Some results of the scaling confirmation factor analysis (SCFA) application in semiconductor gamma-ray spectrometry presented in this contribution points out to a new ground for evaluation the gamma-ray spectra. This whole-spectrum processing approach considerably increases detection sensitivity, especially, if significant interferences being present in the measured spectrum. Precision of the SCFA method is determined by choice of a sufficient number of suitable calibration gamma-ray sources in the energy region of interest, by setting up an acceptable latent hypothesis and by chosen experimental quantification of spectra. The SCFA method is very advantageous to use, for instance, in ultra low-level gamma-spectrometry where counting rates in full energy peaks are extremely low as compared with background interferences. It enables to increase of the sensitivity by the 5-10 times in comparison with the traditional full energy peak net area method (J.K.). 1 fig., 2 tabs., 6 refs.

On response operator in semiconductor gamma ray spectrometry

International Nuclear Information System (INIS)

Krnac, S.; Povinec, P.

1995-01-01

Some results of the scaling confirmation factor analysis (SCFA) application in semiconductor gamma-ray spectrometry presented in this contribution points out to a new ground for evaluation the gamma-ray spectra. This whole-spectrum processing approach considerably increases detection sensitivity, especially, if significant interferences being present in the measured spectrum. Precision of the SCFA method is determined by choice of a sufficient number of suitable calibration gamma-ray sources in the energy region of interest, by setting up an acceptable latent hypothesis and by chosen experimental quantification of spectra. The SCFA method is very advantageous to use, for instance, in ultra low-level gamma-spectrometry where counting rates in full energy peaks are extremely low as compared with background interferences. It enables to increase of the sensitivity by the 5-10 times in comparison with the traditional full energy peak net area method (J.K.). 1 fig., 2 tabs., 6 refs

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

African Journals Online (AJOL)

NIJOTECH

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

Standard guide for high-resolution gamma-ray spectrometry of soil samples

CERN Document Server

American Society for Testing and Materials. Philadelphia

2004-01-01

1.1 This guide covers the identification and quantitative determination of gamma-ray emitting radionuclides in soil samples by means of gamma-ray spectrometry. It is applicable to nuclides emitting gamma rays with an approximate energy range of 20 to 2000 keV. For typical gamma-ray spectrometry systems and sample types, activity levels of about 5 Bq (135 pCi) are measured easily for most nuclides, and activity levels as low as 0.1 Bq (2.7 pCi) can be measured for many nuclides. It is not applicable to radionuclides that emit no gamma rays such as the pure beta-emitting radionuclides hydrogen-3, carbon-14, strontium-90, and becquerel quantities of most transuranics. This guide does not address the in situ measurement techniques, where soil is analyzed in place without sampling. Guidance for in situ techniques can be found in Ref (1) and (2). This guide also does not discuss methods for determining lower limits of detection. Such discussions can be found in Refs (3), (4), (5), and (6). 1.2 This guide can be us...

Determination of chlorine in coal by X-ray fluorescence spectrometry method

Energy Technology Data Exchange (ETDEWEB)

Marek, S.; Bojarska, K. [Central Mining Institute, Katowice (Poland). Dept. of Environmental Monitoring

1997-12-31

Determination of chlorine contents in coal is essential for both environmental protection and its technological use. The existing method of chlorine determination in coal are titration methods which have considerable errors particularly in the low concentration range. The elaborated method with the use of X-ray fluorescence spectrometry in a comparison to the other methods is much faster and has better precision and accuracy. The principle of the method lies in the measurement of X-ray fluorescence radiation intensity which is emitted by chlorine in a sample and its comparison with standards. The calibration of the elaborated XRF method is based on natural coals having various concentrations of chlorine within the whole range of its occurrence in Polish coals. Concentrations for the calibration purpose were obtained by the determination of chlorine contents in selected coals by atomic absorption spectrometry method. The procedure of sample preparation for direct X-ray measurements, instrumental measuring conditions and the way of calibration curve preparation are described in the paper. All X-ray measurements were done with a Phillips sequential X-ray fluorescence spectrometer. A double anode Cr-Au X-ray tube with maximum power 3000 MW was used as the excitation source. 5 figs., 4 tabs.

Is scanning electron microscopy/energy dispersive X-ray spectrometry (SEM/EDS) quantitative?

Science.gov (United States)

Newbury, Dale E; Ritchie, Nicholas W M

2013-01-01

Scanning electron microscopy/energy dispersive X-ray spectrometry (SEM/EDS) is a widely applied elemental microanalysis method capable of identifying and quantifying all elements in the periodic table except H, He, and Li. By following the "k-ratio" (unknown/standard) measurement protocol development for electron-excited wavelength dispersive spectrometry (WDS), SEM/EDS can achieve accuracy and precision equivalent to WDS and at substantially lower electron dose, even when severe X-ray peak overlaps occur, provided sufficient counts are recorded. Achieving this level of performance is now much more practical with the advent of the high-throughput silicon drift detector energy dispersive X-ray spectrometer (SDD-EDS). However, three measurement issues continue to diminish the impact of SEM/EDS: (1) In the qualitative analysis (i.e., element identification) that must precede quantitative analysis, at least some current and many legacy software systems are vulnerable to occasional misidentification of major constituent peaks, with the frequency of misidentifications rising significantly for minor and trace constituents. (2) The use of standardless analysis, which is subject to much broader systematic errors, leads to quantitative results that, while useful, do not have sufficient accuracy to solve critical problems, e.g. determining the formula of a compound. (3) EDS spectrometers have such a large volume of acceptance that apparently credible spectra can be obtained from specimens with complex topography that introduce uncontrolled geometric factors that modify X-ray generation and propagation, resulting in very large systematic errors, often a factor of ten or more. © Wiley Periodicals, Inc.

X-Ray Spectrometry for Preventive Conservation Research

International Nuclear Information System (INIS)

Grieken, V. R.

2008-01-01

Preventive conservation studies the influence of environmental conditions on the durability of works of art. X-ray spectrometry (XRS), in its many forms, is one of the main physical analysis techniques used in the context of cultural heritage in view of its non-destructive nature; it is also highly indicated for studying the composition of e.g. harmful atmospheric particles in e.g. museums. A short literature overview will be to illustrate the important role of XRS in conservation. Then some of our own applications of XRS (especially automated electron probe X-ray microanalysis for individual atmospheric particles) will be shown. These include studies in the Wawel Castle in Cracow, Poland (where outdoor soot nanoparticles and deicing salts brought in by visitors were most threatening for the wall tapestry collections) and the Metropolitan Museum in New York, USA (where sodium nitrate particles from the reaction of sea spray with car exhaust gases were predominant in some rooms)

Elements in normal and cirrhotic human liver. Potassium, iron, copper, zinc and bromine measured by X-ray fluorescence spectrometry

DEFF Research Database (Denmark)

Laursen, J.; Milman, N.; Leth, Peter Mygind

1990-01-01

Various elements (K, Fe, Cu, Zn, Br) were measured by X-ray flourescence spectrometry in cellular and connective tissue fractions of normal and cirrhotic liver samples obtained at autopsy. Normal livers: 32 subjects (16 males, 16 females) median age 69 years. Cirrhotic livers: 14 subjects (13 mal...

New possibilities in prompt gamma ray spectrometry

Energy Technology Data Exchange (ETDEWEB)

Borderie, B; Barrandon, J N [Centre National de la Recherche Scientifique, 45 - Orleans-la-Source (France). Lab. du cyclotron; Pinault, J L [Bureau de Recherches Geologiques et Minieres (BRGM), 45 - Orleans (France)

1977-01-01

Prompt gamma ray spectrometry has been used as an analytical tool for many years. The high level of background noise does, however, remain a major problem with this technique. From simple theoretical consideration, conditions (particle, energy) were determined to reduce significantly the background noise under irradiation. Alpha particles of 3.5 MeV were chosen. Some fifty elements were studied, of which 24 gave interesting results. The detection limits obtained for a sample of niobium were as follows: approximately 1 ppm (10/sup -6/g/g) for the light elements Li, B, F and Na, and between 50 ppm and 1% for the others. Numerous applications may be envisaged in the geo- and cosmo-sciences.

Further development of IDGS: Isotope dilution gamma-ray spectrometry

International Nuclear Information System (INIS)

Li, T.K.; Parker, J.L.; Kuno, Y.; Sato, S.; Kamata, M.; Akiyama, T.

1991-01-01

The isotope dilution gamma-ray spectrometry (IDGS) technique for determining the plutonium concentration and isotopic composition of highly radioactive spent-fuel dissolver solutions has been further developed. Both the sample preparation and the analysis have been improved. The plutonium isotopic analysis is based on high-resolution, low-energy gamma-ray spectrometry. The plutonium concentration in the dissolver solutions then is calculated from the measured isotopic differences among the spike, the dissolver solution, and the spiked dissolver solution. Plutonium concentrations and isotopic compositions of dissolver solutions analyzed from this study agree well with those obtained by traditional isotope dilution mass spectrometry (IDMS) and are consistent with the first IDGS experimental result. With the current detector efficiency, sample size, and a 100-min count time, the estimated precision is ∼0.5% for 239 Pu and 240 Pu isotopic analyses and ∼1% for the plutonium concentration analysis. 5 refs., 2 figs., 7 tabs

Simple circuit for precise measurement of live dead or clock time in gamma-ray spectrometry

International Nuclear Information System (INIS)

Hammer, W.; Sterlinski, S.

1976-01-01

The basic design features and characteristics of circuit are described in the paper. The circuit coupled to a multichannel analyser (MCA) enables one of times: live(Tsub(iota)), dead (Tsub(d)) or clock(Tsub(c)) to be measured precisely. Second one is measured by a built-in timer of MCA. Having the Tsub(c)/Tsub(iota) ratio and utilizing suitable mathematical formulas one can make the corrections for both main effects (dead-time and pile-up) which yield counting losses in gamma-ray spectrometry at high and/or variable activities. Two examples of the dead-time and pile-up corrections by using the new circuit are presented in this paper. (author)

Demonstration of a collimated in situ method for determining depth distributions using gamma-ray spectrometry

CERN Document Server

Benke, R R

2002-01-01

In situ gamma-ray spectrometry uses a portable detector to quantify radionuclides in materials. The main shortcoming of in situ gamma-ray spectrometry has been its inability to determine radionuclide depth distributions. Novel collimator designs were paired with a commercial in situ gamma-ray spectrometry system to overcome this limitation for large area sources. Positioned with their axes normal to the material surface, the cylindrically symmetric collimators limited the detection of un attenuated gamma-rays from a selected range of polar angles (measured off the detector axis). Although this approach does not alleviate the need for some knowledge of the gamma-ray attenuation characteristics of the materials being measured, the collimation method presented in this paper represents an absolute method that determines the depth distribution as a histogram, while other in situ methods require a priori knowledge of the depth distribution shape. Other advantages over previous in situ methods are that this method d...

Development of a portable system of X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Mantuano, Andrea; Crisostomo, Jose V.V.; Barros, Mariana J.; Oliveira, Luis F.; Barroso, Regina C.

2009-01-01

This paper develops a compact and portable spectrometry system that will be used at the Laboratory of Applied Physics to the Biomedical and Environmental Sciences of the Institute of Physics/UERJ, Rio de Janeiro, Brazil. The laboratory both prepares the samples and develops the X-ray spectrometry techniques. The techniques of X-ray diffraction and fluorescence on various samples (biological, industrial and environmental) are used, attending to pos-graduation and graduation students, with multidisciplinary characteristics. The Mini-X system consists of X-ray mini tube MINI-X from Amptek with tungsten (W) target, and a compact spectrometer X123, also from Amptek that includes a detector, pre-amplifier, digital pulse processor, and multichannel. All the system is controlled by dedicated microprocessor. This work will present both a methodology for alignment and calibration of the system as far the first measurements performed using the X-ray fluorescence technique on standard samples. The multi elementary analysis by X-ray fluorescence (XRF) is based on the measurements of the characteristic X-ray intensity emitted by the chemical elements components of the samples when excited. Therefore, from the development of this compact and versatile system it will be possible to obtain the fluorescent intensities of the analysed samples at the Laboratory, not only at the research area but at the teaching area. Besides, new laboratory practices are being developed for the discipline of medical physics

X-ray fluorescence and gamma-ray spectrometry combined with multivariate analysis for topographic studies in agricultural soil

International Nuclear Information System (INIS)

Castilhos, Natara D.B. de; Melquiades, Fábio L.; Thomaz, Edivaldo L.; Bastos, Rodrigo Oliveira

2015-01-01

Physical and chemical properties of soils play a major role in the evaluation of different geochemical signature, soil quality, discrimination of land use type, soil provenance and soil degradation. The objectives of the present study are the soil elemental characterization and soil differentiation in topographic sequence and depth, using Energy Dispersive X-Ray Fluorescence (EDXRF) as well as gamma-ray spectrometry data combined with Principal Component Analysis (PCA). The study area is an agricultural region of Boa Vista catchment which is located at Guamiranga municipality, Brazil. PCA analysis was performed with four different data sets: spectral data from EDXRF, spectral data from gamma-ray spectrometry, concentration values from EDXRF measurements and concentration values from gamma-ray spectrometry. All PCAs showed similar results, confirmed by hierarchical cluster analysis, allowing the data grouping into top, bottom and riparian zone samples, i.e. the samples were separated due to its landscape position. The two hillslopes present the same behavior independent of the land use history. There are distinctive and characteristic patterns in the analyzed soil. The methodologies presented are promising and could be used to infer significant information about the region to be studied. - Highlights: • Characterization of topographic sequence of two hillslopes from agricultural soil. • Employment of EDXRF and gamma-ray spectrometry data combined with PCA. • The combination of green analytical methodologies with chemometric studies allowed soil differentiation. • The innovative methodology is promising for direct characterization of agricultural catchments

Soft X ray spectrometry at high count rates

International Nuclear Information System (INIS)

Blanc, P.; Brouquet, P.; Uhre, N.

1978-06-01

Two modifications of the classical method of X-ray spectrometry by a semi-conductor diode permit a count rate of 10 5 c/s with an energy resolution of 350 eV. With a specially constructed pulse height analyzer, this detector can measure four spectra of 5 ms each, in the range of 1-30 keV, during a plasma shot

Determination of 239Pu and 240Pu isotope ratio for a nuclear bomb particle using X-ray spectrometry in conjunction with γ-ray spectrometry and non-destructive α-particle spectrometry

International Nuclear Information System (INIS)

Poellaenen, R.; Ruotsalainen, K.; Toivonen, H.

2009-01-01

A nuclear bomb particle from Thule containing Pu and U was analyzed using X-ray spectrometry in combination with γ-ray spectrometry and non-destructive α-spectrometry. The main objective was to investigate the possibility to determine the 239 Pu and 240 Pu isotope ratios. Previously, X-ray spectrometry together with the above-mentioned methods has been successfully applied for radiochemically processed samples, but not for individual particles. In the present paper we demonstrate the power of non-destructive analysis. The 239 Pu/( 239 Pu+ 240 Pu) atom ratio for the Thule particle was determined, using two different approaches, to be 0.93±0.07 and 0.91±0.05. These results are consistent with weapons-grade material and the results obtained by other investigators.

Janus probe, a detection system for high energy reactor gamma-ray spectrometry

International Nuclear Information System (INIS)

Gold, R.; Kaiser, B.J.

1980-03-01

In reactor environments, gamma-ray spectra are continuous and the absolute magnitude as well as the general shape of the gamma continuum are of paramount importance. Consequently, conventional methods of gamma-ray detection are not suitable for in-core gamma-ray spectrometry. To meet these specific needs, a method of continuous gamma-ray spectrometry, namely Compton Recoil Gamma-Ray Spectrometry, was developed for in-situ observations of reactor environments. A new gamma-ray detection system has been developed which extends the applicability of Compton Recoil Gamma-Ray Spectrometry up to roughly 7 MeV. This detection system is comprised of two separate Si(Li) detectors placed face-to-face. Hence this new detection system is called the Janus probe. Also shown is the block diagram of pulse processing instrumentation for the Janus probe. This new gamma probe not only extends the upper energy limit of in-core gamma-ray spectrometry, but in addition possesses other fundamental advantages

X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Vries, J.L. de.

1976-01-01

The seventh edition of Philips' Review of Literature on x-ray fluorescence spectrometry starts with a list of conference proceedings on the subject, organised by the Philips organisation at regular intervals in various European countries. It is followed by a list of bulletins. The bibliography is subdivided according to spectra, equipment, applications and absorption analysis

Development of isotope dilution gamma-ray spectrometry for plutonium analysis

Energy Technology Data Exchange (ETDEWEB)

Li, T.K.; Parker, J.L. (Los Alamos National Lab., NM (United States)); Kuno, Y.; Sato, S.; Kurosawa, A.; Akiyama, T. (Power Reactor and Nuclear Fuel Development Corp., Tokai, Ibaraki (Japan))

1991-01-01

We are studying the feasibility of determining the plutonium concentration and isotopic distribution of highly radioactive, spent-fuel dissolver solutions by employing high-resolution gamma-ray spectrometry. The study involves gamma-ray plutonium isotopic analysis for both dissolver and spiked dissolver solution samples, after plutonium is eluted through an ion-exchange column and absorbed in a small resin bead bag. The spike is well characterized, dry plutonium containing {approximately}98% of {sup 239}Pu. By using measured isotopic information, the concentration of elemental plutonium in the dissolver solution can be determined. Both the plutonium concentration and the isotopic composition of the dissolver solution obtained from this study agree well with values obtained by traditional isotope dilution mass spectrometry (IDMS). Because it is rapid, easy to operate and maintain, and costs less, this new technique could be an alternative method to IDMS for input accountability and verification measurements in reprocessing plants. 7 refs., 4 figs., 4 tabs.

X-ray spectrometry for preventive conservation of cultural heritage

Indian Academy of Sciences (India)

Analytical chemistry does play a key role in the chemical characterization of the environment and it appears that X-ray spectrometry, in its many forms, is one of the most relevant analytical techniques in preventive conservation, as it is in cultural heritage research in general. X-ray spectrometry has indeed been the method ...

The determination of molybdenum and tungsten in resin by x-ray-fluorescence spectrometry

International Nuclear Information System (INIS)

Eddy, B.T.

1985-01-01

This report describes a method using X-ray-fluorescence spectrometry for the determination of molybdenum and tungsten in ion-exchange resins. The dried resin is milled with sand, binder, and an internal-standard mixture before being briquetted. Niobium and zinc are used as the internal standards for molybdenum and tungsten respectively. Intensity measurements are made with the gold anode tube. Corrections are made for the interference of the Mo Kα analytical line on the background intensities used for the Mo Kα and Nb Kα lines. The precision of the analysis for molybdenum ranges from a relative standard deviation 0,02 at 5 mg/g to 0.045 at 55μg/g; for tungsten, the relative standard deviation ranges from 0,04 at 5 mg/g to 0,055 at 55μg/g. The limits of determination in the original resin sample were found to be 40μg/g for molybdenum and 80μg/g for tungsten. The laboratory method is given in an appendix

New portability for in situ gamma-ray spectrometry from commercially available equipment

International Nuclear Information System (INIS)

Stanford, N.; Laurenzo, E.L.; McCurdy, D.E.

1984-01-01

In situ gamma-ray spectrometry has been employed by the staff of the Yankee Atomic Environmental Laboratory on a routine basis for more than five years. The original in situ gamma-ray spectrometry methodology was adopted from the techniques developed at the DOE Environmental Measurements Laboratory (Beck, DeCampo, and Gogolak 1972). The system consisted of a 110 cm 3 Ge(Li) detector in the vertical configuration in conjunction with typical laboratory nuclear instrumentation, as well as a medium-sized desktop computer, printer and disk drive. The equipment was transported in a small van having a shock-mounted cabinet and gasoline generator as an electrical power source. Recent availability of miniaturized spectrometry systems and powerful portable computers has enabled the upgrading of the 1977 vintage equipment to a system which is truly portable, light weight, compact and more reliable. The system to be described utilizes a portable intrinsic germanium detector, a small, 4096 channel pulse height analyzer (MCA) with anscillary components and a 24K, Hewlett Packard HP-75 computer with a small tape drive. When the equipment is used in the field, the system has enough capability to acquire and store a full 4096 channel gamma-ray spectrum and calculate the soil concentrations (pCi/g) and/or external radiation exposure rates for the commonly found naturally occurring, long-lived atmospheric nuclear weapons testing and nuclear power plant radionuclides. Subsequent data transfer to a larger desktop computer via available interfacing at the laboratory enables a full peak search and a more extensive evaluation of the data in order to calculate the soil concentrations and/or external radiation exposure rates for a selected 25 radionuclides. Experiences from the first season of operation are discussed

Research on 3-D terrain correction methods of airborne gamma-ray spectrometry survey

International Nuclear Information System (INIS)

Liu Yanyang; Liu Qingcheng; Zhang Zhiyong

2008-01-01

The general method of height correction is not effectual in complex terrain during the process of explaining airborne gamma-ray spectrometry data, and the 2-D terrain correction method researched in recent years is just available for correction of section measured. A new method of 3-D sector terrain correction is studied. The ground radiator is divided into many small sector radiators by the method, then the irradiation rate is calculated in certain survey distance, and the total value of all small radiate sources is regarded as the irradiation rate of the ground radiator at certain point of aero- survey, and the correction coefficients of every point are calculated which then applied to correct to airborne gamma-ray spectrometry data. The method can achieve the forward calculation, inversion calculation and terrain correction for airborne gamma-ray spectrometry survey in complex topography by dividing the ground radiator into many small sectors. Other factors are considered such as the un- saturated degree of measure scope, uneven-radiator content on ground, and so on. The results of for- ward model and an example analysis show that the 3-D terrain correction method is proper and effectual. (authors)

Spatially-Dependent Measurements of Surface and Near-Surface Radioactive Material Using In situ Gamma Ray Spectrometry (ISGRS) For Final Status Surveys

International Nuclear Information System (INIS)

J. A. Chapman, A. J. Boerner, E. W. Abelquist

2006-01-01

In-situ, high-resolution gamma-ray spectrometry (ISGRS) measurements were conducted at the Oak Ridge Institute for Science and Education ORISE field laboratory in Oak Ridge, Tennessee. The purpose of these tests was to provide analytical data for assessing how 'fit for use' this technology is for detecting discrete particles in soil

Spatially-Dependent Measurements of Surface and Near-Surface Radioactive Material Using In situ Gamma Ray Spectrometry (ISGRS) For Final Status Surveys

Energy Technology Data Exchange (ETDEWEB)

J. A. Chapman, A. J. Boerner, E. W. Abelquist

2006-11-15

In-situ, high-resolution gamma-ray spectrometry (ISGRS) measurements were conducted at the Oak Ridge Institute for Science and Education (ORISE) field laboratory in Oak Ridge, Tennessee. The purpose of these tests was to provide analytical data for assessing how “fit for use” this technology is for detecting discrete particles in soil.

Carborne gamma-ray spectrometry. Calibration and applications

International Nuclear Information System (INIS)

Aage, H.K.; Korsbech, U.; Bargholz, K.; Hovgaard, J.

2006-01-01

Calibration of carborne gamma-ray spectrometry systems for 137 Cs is carried out with a source successively placed at 791 positions within an area of 34 mx62 m. A computer model supplements the measurements. Hereby a sensitivity map for a surface contamination is generated as well as line and area sensitivities. Another model converts surface sensitivity to sensitivity for a deep contamination. Use of the sensitivity map for a non-homogeneous distribution of 137 Cs is demonstrated. Applications of line sensitivities for special tasks are discussed

Conformational analysis of g protein-coupled receptor signaling by hydrogen/deuterium exchange mass spectrometry.

Science.gov (United States)

Li, Sheng; Lee, Su Youn; Chung, Ka Young

2015-01-01

Conformational change and protein-protein interactions are two major mechanisms of membrane protein signal transduction, including G protein-coupled receptors (GPCRs). Upon agonist binding, GPCRs change conformation, resulting in interaction with downstream signaling molecules such as G proteins. To understand the precise signaling mechanism, studies have investigated the structural mechanism of GPCR signaling using X-ray crystallography, nuclear magnetic resonance (NMR), or electron paramagnetic resonance. In addition to these techniques, hydrogen/deuterium exchange mass spectrometry (HDX-MS) has recently been used in GPCR studies. HDX-MS measures the rate at which peptide amide hydrogens exchange with deuterium in the solvent. Exposed or flexible regions have higher exchange rates and excluded or ordered regions have lower exchange rates. Therefore, HDX-MS is a useful tool for studying protein-protein interfaces and conformational changes after protein activation or protein-protein interactions. Although HDX-MS does not give high-resolution structures, it analyzes protein conformations that are difficult to study with X-ray crystallography or NMR. Furthermore, conformational information from HDX-MS can help in the crystallization of X-ray crystallography by suggesting highly flexible regions. Interactions between GPCRs and downstream signaling molecules are not easily analyzed by X-ray crystallography or NMR because of the large size of the GPCR-signaling molecule complexes, hydrophobicity, and flexibility of GPCRs. HDX-MS could be useful for analyzing the conformational mechanism of GPCR signaling. In this chapter, we discuss details of HDX-MS for analyzing GPCRs using the β2AR-G protein complex as a model system. © 2015 Elsevier Inc. All rights reserved.

40 K, 137 Cs and 232 Th activities in Brazilian milk samples measured by gamma ray spectrometry

International Nuclear Information System (INIS)

Melquiades, Fabio L.; Appoloni, Carlos R.

2000-01-01

This work deals with the measurement of radioactive activities in powdered milk, with high resolution gamma-ray spectrometry, using a HPGe detector coupled to a standard electronic nuclear chain and a multichannel card of 8192 channels. Preliminary measurements were accomplished to define the kind of the system shield, the geometry of the sample recipient, the size of the sampling and the self absorption correction. It was possible to measure the radionuclides 40 K, 137 Cs and 208 Tl, whose activities were calculated according to the International Atomic Energy Agency norms. The detector efficiency was measured employing calibrated samples, prepared with IAEA certificate standards mixed with powdered milk. Tukey's average comparison test was used to check the repeatability of the measurements and the absence of significant systematic deviation. (author)

Significance of radioelement concentration measurements made by airborne gamma-ray spectrometry over the Canadian Shield

International Nuclear Information System (INIS)

Charbonneau, B.W.; Killeen, P.G.; Carson, J.M.; Cameron, G.W.; Richardson, K.A.

1976-01-01

Results of airborne gamma-ray spectrometer surveys conducted by the Geological Survey of Canada are presented as maps contoured in units of radioelement and concentration ratios. These contoured values represent the average surface concentrations of the radioelements over areas of the order of several square kilometres. The relationship between this ''average surface concentration'' and the radioelement concentration in bedrock underlying the area depends on: (1) the percentage of outcrop; (2) the relation between overburden and bedrock radioelement concentration; (3) percentage of marshland or surface water in the area; (4) soil moisture; and (5) density of vegetation. More than 2500 portable gamma-ray spectrometer analyses of outcrop and overburden have been made in the Bancroft, Elliot Lake and Fort Smith areas of the Canadian Precambrian Shield. In the areas examined, the radioelement concentrations in glacial drift reflect the concentrations in the underlying bedrock. Rocks with near-crustal average contents of thorium, uranium and potassium are overlain by glacial drift having approximately the same concentrations. As the concentration in bedrock increases, the concentration in the local overburden also increases, but not to the same extent. In addition, in-situ gamma-ray spectrometry measurements were made at almost 1000 stations within the area of airborne surveys near Mont Laurier and Elliot Lake. These ground measurements were compared with the airborne measurements by averaging the values for all those ground stations located in the areas between each contour level on airborne maps. Radioelement concentrations in bedrock are considerably higher than corresponding airborne measurements, and this difference between bedrock and airborne values increases at higher radioelement concentrations. Radioelement concentrations in glacial drift are only slightly higher than airborne contour values for the same area. Airborne contour maps of the radioelement ratios

Radiochemical separation of {sup 231}Pa from siliceous cake prior to its determination by gamma ray spectrometry

Energy Technology Data Exchange (ETDEWEB)

Dalvi, Aditi A. [Bhabha Atomic Research Centre, Mumbai (India). Analytical Chemistry Div.; Homi Bhabha National Institute, Mumbai (India); Verma, Rakesh

2017-07-01

A simple and fast radiochemical method for the separation of protactinium ({sup 231}Pa) from siliceous cake for its determination by gamma ray spectrometry is described. The method involves (a) a novel approach, the fusion of the siliceous cake with sodium peroxide, (b) the dissolution of the fused mass in nitric acid and (c) the co-precipitation of {sup 231}Pa with manganese dioxide formed in-situ by the addition of solid manganous sulfate and potassium permanganate to the solution. The fusion, effected in a single step, is simpler and highly effective in comparison to methods reported hitherto in literature. The radiochemical yield of {sup 231}Pa, determined using 311.9 keV gamma ray of {sup 233}Pa radiotracer is quantitative (∝90%). The decontamination factors calculated using gamma ray spectrometry and energy dispersive X-ray fluorescence measurements show that the separation from the interfering radionuclides is high whereas separation from major and minor elements is good. Separation by ion-exchange method in hydrochloric acid, hydrofluoric acid and oxalic acid media have comparatively much lower yields. The concentration of {sup 231}Pa in the siliceous cake measured using interference-free 283.6 keV gamma ray was found to be (6.4 ± 0.33) μg kg{sup -1}. The measured concentration of {sup 231}Pa was well above the limit of quantitation whereas the coefficient of variation was ∝5%. The improvement in the limit of detection was due to the reduction in spectral background. Systematic evaluation of various uncertainty parameters showed that the major contributors to the combined uncertainty were efficiency of the high purity germanium detector and the counting statistics. The present sample decomposition and separation methods are robust, simple to perform and can be effectively used for the determination and hence source prospecting of protactinium.

Working with Detection Limits in X-Ray and Nuclear Spectrometry

International Nuclear Information System (INIS)

Van Espen, P.

2003-01-01

Full Text: Detection limits are important in many measurement procedures. Especially in analytical work we often need to take a decision about the presence or absence of a compound, or we need to guarantee that or instrument can detect the compound. Especially in regulatory work the concept of detection limits plays a crucial role. Data acquisition in x-ray and gamma-ray spectrometry is done by counting events for a preset time; hence the fluctuations in the observed spectra are governed by Poisson (counting) statistics. This makes the calculation of detection limits in principle very easy. However it is observed that there exists a great deal of confusion concerning the definition(s) and especially concerning the practical calculation and reporting of detection limits. In this contribution a simple but rigorous treatment of the concept of detection limits will be given, emphasizing on aspects such as a-priori and a-posterior i limits and on the effect of sample blank and instrumental blank in the calculation of the true detection limit. The problem of near zero background as observed in e.g. total reflection x-ray fluorescence analysis (T-XRF) and some low level counting applications will also be discussed. In this case Poisson statistics might not be applicable, affecting the decision limits with respect to the presence of absence of a signal. Finally handling data sets that contain detection limit values next to normal measured values, the so called problem of missing data will be discussed. Some suggestions to deal with this frequently occurring situation will be given

Optimization of measure parameters for an X- and gamma-ray spectrometry portable system

International Nuclear Information System (INIS)

Fernandes, Jaquiel S.; Appoloni, Carlos R.

2008-01-01

In order to optimize the use of a system for in situ gamma (γ)- and X-ray spectrometry composed of a 3x3x1 mm 3 Cadmium Telluride (CdTe) detector with respect to the detection of low-activity radioactive sources, a two level factorial planning was accomplished, involving three factors that could modify the system response. This planning was made with a 137 Cs punctual source, analyzing the X-ray energy line of 32 keV from 137m Ba. It was concluded that, for the system optimization, the best configuration for the involved parameters was to work with the detector at temperature of -22 o C, shaping time of 3 μs and rise time discrimination (RTD) with value 3

Compilation of monographs on α-, β-, γ- and X-ray spectrometry

International Nuclear Information System (INIS)

Debertin, K.

1977-11-01

The working group 'α-, β-, γ-Ray Spectrometry' of the International Committee for Radionuclide Metrology (ICRM) compiled about 35 monographs on α-, β-, γ- and X-ray spectrometry which were published in the years 1970 to 1976. Support was obtained by the Zentralstelle fuer Atomkernenergie-Dokumentation (ZAED) in Karlsruhe. (orig.) [de

Correcting the effects of the matrix using capture gamma-ray spectrometry: Application to measurement by Active Neutron Interrogation; Correction des effets de matrice par spectrometrie des rayonnements gamma de capture: Application a la mesure par Interrogation Neutronique Active (I.N.A.)

Energy Technology Data Exchange (ETDEWEB)

Baudry, G.

2003-11-15

In the field of the measurement of low masses of fissile material ({sup 235}U, {sup 239}Pu, {sup 241}Pu) in radioactive waste drums, the Active Neutron Interrogation is a non-destructive method achieving good results. It does however remain reliant upon uncertainties related to the matrix effects on interrogation and fission neutrons. The aim of this thesis is to develop a correction method able to take into account these matrix effects by quantifying the amount of absorbent materials (chlorine and hydrogen) in a 118- liter homogeneous matrix. The main idea is to use the gamma-ray spectrometry of gamma emitted by neutron captures to identify and quantify the composition of the matrix. An indicator from its chlorine content is then deduced in order to choose the calibration coefficient which best represents the real composition of the matrix. This document firstly presents the needs of control and characterization of radioactive objects, and the means used in the field of nuclear measurement. Emphases is put in particular on the Active Neutron Interrogation method. The matrices of interest are those made of light technological waste (density {<=} 0,4 g/cm{sup 3}) containing hydrogenated and chlorinated materials. The advantages of gamma-rays emitted by neutron captures for the determination of a chlorine content indicator of the matrices and the principles of the correction method are then explained. Measurements have been firstly realized with an existing Neutron Interrogation device (PROMETHEE 6). Such measurements have proven its inadequacy: no signal from the matrix hydrogen was detected, due to an intense signal from the polyethylene contained in some cell elements. Moreover, the matrix chlorine content appeared difficult to be measured. A new and specific device, named REGAIN and dedicated to active gamma-rays spectrometry, was defined with the Monte-Carlo N-Particle (MCNP) code. The experiments conducted with this new device made it possible to detect the

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

International Nuclear Information System (INIS)

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

2006-01-01

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

Measurement control for plutonium isotopic measurements using gamma-ray spectrometry

International Nuclear Information System (INIS)

Fleissner, J.G.

1985-01-01

A measurement control (MC) program should be an integral part of every nondestructive assay measurement system used for the assay of special nuclear materials. This report describes an MC program for plutonium isotopic composition measurements using high-resolution gamma-ray spectroscopy. This MC program emphasizes the standardization of data collection procedures along with the implementation of internal and external measurement control checks to provide the requisite measurement quality assurance. This report also describes the implementation of the MC program in the isotopic analysis code GRPAUT. Recommendations are given concerning the importance and frequency of the various MC checks in order to ensure a successful implementation of the MC procedures for the user's application

A new approach for the high-precision determination of the elemental uranium concentration in uranium ore by gamma-ray spectrometry

International Nuclear Information System (INIS)

Nagel, W.; Quik, F.

1993-01-01

A new approach for the determination of elemental uranium in uranium bearing ore, using high resolution gamma-ray spectrometry, was applied. Using a variant of the enrichment meter technique an agreement of better than 1% has been obtained between gamma-ray measurement results and the certified value obtained by other analytical methods. For the calibration of the gamma-ray spectrometer uranium reference samples have been used which are made available jointly in Europe and the USA as Certified Reference Materials for Gamma-ray Spectrometry (EC NRM 171 and NBS SRM 969, respectively). The measured ore has been put in a special designed container which ensured in all directions seen from the radiation window a uniform degree of infinite thickness of about 95%. The measurement results can be taken as an example for the applicability of gamma-ray spectrometry when high accuracy is required and under conditions where homogeneous distributed elemental uranium is embedded in a larger amount of matrix material. (author). 8 refs., 10 figs., 2 tabs., 2 appendices

Spectrum unfolding in X-ray spectrometry using the maximum entropy method

International Nuclear Information System (INIS)

Fernandez, Jorge E.; Scot, Viviana; Di Giulio, Eugenio

2014-01-01

The solution of the unfolding problem is an ever-present issue in X-ray spectrometry. The maximum entropy technique solves this problem by taking advantage of some known a priori physical information and by ensuring an outcome with only positive values. This method is implemented in MAXED (MAXimum Entropy Deconvolution), a software code contained in the package UMG (Unfolding with MAXED and GRAVEL) developed at PTB and distributed by NEA Data Bank. This package contains also the code GRAVEL (used to estimate the precision of the solution). This article introduces the new code UMESTRAT (Unfolding Maximum Entropy STRATegy) which applies a semi-automatic strategy to solve the unfolding problem by using a suitable combination of MAXED and GRAVEL for applications in X-ray spectrometry. Some examples of the use of UMESTRAT are shown, demonstrating its capability to remove detector artifacts from the measured spectrum consistently with the model used for the detector response function (DRF). - Highlights: ► A new strategy to solve the unfolding problem in X-ray spectrometry is presented. ► The presented strategy uses a suitable combination of the codes MAXED and GRAVEL. ► The applied strategy provides additional information on the Detector Response Function. ► The code UMESTRAT is developed to apply this new strategy in a semi-automatic mode

Gamma-ray spectrometry laboratory and in situ: developments and environmental applications

International Nuclear Information System (INIS)

Gasser, Estelle

2014-01-01

Gamma-ray spectrometry enables determining all γ-ray emitters in a sample with a single measurement. Self-absorption of γ-rays in samples is manifest by a loss or a gain of pulses that results in a poor estimation of the counting efficiency. To characterize a new counting geometry improvements of the existing set-up were made with MCNPX simulations. With the new geometry we could specify absorbed and annual effective doses as well as dose conversion factors for the natural radioisotopes of several building materials and soil samples. Simulations show the influence of detection limits of γ-radiation on dose conversion factors and the need for updating these factors. γ-ray measurements of soil in situ require different counting efficiencies simulated by MCNPX for a semi-infinite source. Two in-situ soil analyses were made, one around a nuclear power and the other for a private company. (author)

Computer programs for data reduction and interpretation in plutonium and uranium analysis by gamma ray spectrometry

International Nuclear Information System (INIS)

Singh, R.K.; Moorthy, A.D.; Babbar, R.K.; Udagatti, S.V.

1989-01-01

Non destructive gamma ray have been developed for analysis of isotopic abundances and concentrations of plutonium and uranium in the respective product solutions of a reprocessing plant. The method involves analysis of gamma rays emitted from the sample and uses a multichannel analyser system. Data reduction and interpretation of these techniques are tedious and time consuming. In order to make it possible to use them in routine analysis, computer programs have been developed in HP-BASIC language which can be used in HP-9845B desktop computer. A set of programs, for plutonium estimation by high resolution gamma ray spectrometry and for on-line measurement of uranium by gamma ray spectrometry are described in this report. (author) 4 refs., 3 tabs., 6 figs

Low-resolution gamma-ray measurements of uranium enrichment

International Nuclear Information System (INIS)

Sprinkle, J.K. Jr.; Christiansen, A.; Cole, R.; Collins, M.L.

1996-01-01

Facilities that process special nuclear material perform periodic inventories. In bulk facilities that process low-enriched uranium, these inventories and their audits are based primarily on weight and enrichment measurements. Enrichment measurements determine the 211 U weight fraction of the uranium compound from the passive gamma-ray emissions of the sample. Both international inspectors and facility operators rely on the capability to make in-field gamma-ray measurements of uranium enrichment. These users require rapid, portable measurement capability. Some in-field measurements have been biased, forcing the inspectors to resort to high-resolution measurements or mass spectrometry to accomplish their goals

Determination of plutonium isotopic ratios and total concentration by gamma ray spectrometry

International Nuclear Information System (INIS)

Despres, Michele.

1980-11-01

A non-destructive method of analysis is being investigated for the control in situ of plutonium isotopic composition and total concentration in different matrix without preliminary calibration. The plutonium isotopic composition is determined by gamma-ray spectrometry using germanium detector systems. The same apparatus is used for direct measuring of the total plutonium concentration in solutions or solids by a differential attenuation technique based on two transmitted gamma rays with energies on both sides of the k shell absorption edge of plutonium [fr

Portable gamma-ray spectrometers and spectrometry systems

International Nuclear Information System (INIS)

Shebell, P.

1999-01-01

The current state-of-the-art in portable gamma-ray spectrometers and portable spectrometry systems is discussed. A comparison of detector performance and features of commercially available systems are summarised. Finally, several applications of portable systems are described. (author)

Measurement of natural gamma radiation in building materials from Thellar of Tiruvannamalai Dist, Tamilnadu, India by gamma ray spectrometry

International Nuclear Information System (INIS)

Raghu, Y.; Ravisankar, R.; Chandrasekararn, A.; Vijayagopal, P.; Venkatraman, B.

2016-01-01

The knowledge of natural radioactivity in building materials is an important aspect of or determining the amount of public exposure because people spend most of their time (about 80%) indoors. Further, the knowledge of this radioactivity is useful in setting the standards and national guidelines in regard to the international recommendations and in assessing the associated radiation hazard. In the present work, the concentrations of natural radionuclides were measured in four types of building materials from Thellar of Tiruvannamalai district, Tamilnadu, India using gamma-ray spectrometry and associated radiological hazards are calculated

Accurate γ-ray spectrometry measurements of the half-life of 92Sr

International Nuclear Information System (INIS)

Leconte, P.; Hudelot, J.P.; Antony, M.

2008-01-01

Studies of the nuclear fuel cycle require an accurate knowledge of the energy release from the decay of radioactive nuclides produced in a reactor, including precise half-life data for the short-lived radionuclides. Moreover, short-lived fission products are crucial for fission rate distribution measurements performed in low-power facilities, such as EOLE and MINERVE of CEA Cadarache [Fougeras, P., 2005. EOLE, MINERVE and MASURCA facilities and their associated neutron experimental programs. In: 13th International Conference on Nuclear Engineering, Beijing, China, 16-20 May 2005], and their nuclear decay data need to be known to high precision. For these reasons, the half-life of 92 Sr has been measured to solve a recently observed inconsistency identified with the quoted value in the main nuclear applications libraries (including JEFF3.1): T 1/2 =2.71±0.01 h [Parsa, B., Ashari, A., Goolvard, L., Nobar, Y.M., 1971. Decay scheme of 2.71 h 92 Sr. Nucl. Phys. A 175, 629-640]. An overestimation of 4.5% has been identified in this work, based on two independent methods. Specific γ-ray spectrometry measurements on activated fissile foils have been carried out, using two HPGe detectors. Influencing factors such as net area measurements of photopeaks, pulse pile-up accuracy and dead time corrections in the presence of decaying activity are discussed. A new value has been obtained by combining eight series of measurements: T 1/2 =2.594±0.006 h. The uncertainty has been reduced by a factor of two with respect to previous evaluations. This measured value also shows good agreement with the most recent studies of T 1/2 =2.627±0.009 h [Nir-El, Y., 2003. Private Communications. Soreq Research Centre, Yavne, Israel

Determination of radon concentration in soil gas by gamma-ray spectrometry of olive oil

International Nuclear Information System (INIS)

Al-Azmi, Darwish; Karunakara, N.

2007-01-01

Measurements of radon concentration in soil gas have been carried out using a bubbling system in which the soil gas is drawn through an active pumping to bubble a liquid absorber (olive oil) for the deposition of the soil gas in it. After the bubbling process, the absorber is then taken for gamma-ray measurements. Gamma-ray photopeaks from the 214 Pb and the 214 Bi radon progeny are considered for the detection of the 222 Rn gas to study the concentration levels for radon soil gas. Results for some field measurements were obtained and compared with results obtained using AlphaGuard radon gas monitor. The technique provides a possible approach for the measurements of radon soil gas with gamma-ray spectrometry

Natural Radioactivity in Geological Samples from Algeria by SSNTD and γ-Ray Spectrometry

International Nuclear Information System (INIS)

Belafrites, A.

2009-01-01

Results of Solid State Nuclear Track Detector (SSNTD) measurements of natural radioactivity using contact autoradiography for the determination of uranium and non-contact autoradiography for radon emanation are presented. The study is complemented by gamma -ray spectrometric results. The SSNTD method applied to geological samples has given uranium concentrations consistent with those found by gamma -ray spectrometry. The results for uranium concentration and radon emanation show excellent agreement with the few values available in other works

Uranium measurement by airborne gamma-ray spectrometry

International Nuclear Information System (INIS)

Grasty, R.L.

1975-01-01

In the airborne measurement of uranium, window type gamma-ray spectrometers are used and it is necessary to correct for scattered high energy radiation from thallium 208 in the thorium decay series. This radiation can be scattered in the crystal, in the ground, and in the air. A theory, analogous to the theory of radioactive decay, is developed; it can adequately explain the spectrum buildup in the uranium window for a point source of thorium oxide immersed to different depths in water and for a detector above the water. The theory is extended to predict the buildup as a function of altitude for detectors of different sizes and shows that errors in the airborne measurement of uranium can be significant if no allowance is made for radiation scattered in the ground and in the air

Low-energy X-ray and gamma spectrometry using silicon photodiodes

International Nuclear Information System (INIS)

Silva, Iran Jose Oliveira da

2000-08-01

The use of semiconductor detectors for radiation detection has increased in recent years due to advantages they present in comparison to other types of detectors. As the working principle of commercially available photodiodes is similar to the semiconductor detector, this study was carried out to evaluate the use of Si photodiodes for low energy x-ray and gamma spectrometry. The photodiodes investigated were SFH-205, SFH-206, BPW-34 and XRA-50 which have the following characteristics: active area of 0,07 cm 2 and 0,25 cm 2 , thickness of the depletion ranging from 100 to 200 μm and junction capacitance of 72 pF. The photodiode was polarized with a reverse bias and connected to a charge sensitive pre-amplifier, followed by a amplifier and multichannel pulse analyzer. Standard radiation source used in this experiment were 241 Am, 109 Cd, 57 Co and 133 Ba. The X-ray fluorescence of lead and silver were also measured through K- and L-lines. All the measurements were made with the photodiodes at room temperature.The results show that the responses of the photodiodes very linear by the x-ray energy and that the energy resolution in FWHM varied between 1.9 keV and 4.4 keV for peaks corresponding to 11.9 keV to 59 keV. The BPW-34 showed the best energy resolution and the lower dark current. The full-energy peak efficiency was also determined and it was observed that the peak efficiency decreases rapidly above 50 keV. The resolution and efficiency are similar to the values obtained with other semiconductor detectors, evidencing that the photodiodes used in that study can be used as a good performance detector for low energy X-ray and gamma spectrometry. (author)

Airborne gamma-ray spectrometry and computer data processing

International Nuclear Information System (INIS)

Raghuwanshi, S.S.; Bhishma Kumar; Tewari, S.G.

1993-01-01

The physical basis for the measurement of radioelemental concentrations of U, Th, and K on the surface of the earth by airborne gamma-ray spectrometry (AGRS) are described in this paper. The yield of an infinite radioactive plane source for a particular gamma energy helps to know the sampled volume in AGRS, the ground coverage, the ground resolution, the effective planning of the survey, flight line spacing, and sampling time. The infinite source-yield enables the determination of the attenuation coefficients in actual surveys and lays down the criteria for a standard test strip. Scattering of gamma-rays in matter is discussed in order to study its influence in the measurements from air. The theoretical gamma-ray spectrum from terrestrial U, Th, and K are discussed in contrast to its realistic picture which poses problems for their direct use for measurements. The criterion of FWHM (full width at half maximum) and inter-energy distance with their yields is described which finally helps to select the energy windows for (window and MCA) AGRS system. Factors which affect the measurements of radioelemental concentration in AGRS surveys include both correctable and non-correctable ones. Correctable factors are : (a) non-terrestrial sources of gamma-rays aircraft, cosmic, and airborne background (H) (B); (b) interference due to gamma-scattering inter channel effects (l); (c) height variations (H) due to navigation and topography; (d) temperature (T) of ambient air; and (e) pressure (P) of air at flying altitude. For removal of background effects, measurements over test strip and calibration pads are necessary for making the corrections in the order - BIH. These methods are described in the paper. The non-correctable factors include effects, due to terrain moisture, vegetation, and others. The possible ways to eliminate these effects are also briefly described. (author). 17 refs., 13 figs

Recent trends in total reflection X-ray fluorescence spectrometry for biological applications

International Nuclear Information System (INIS)

Szoboszlai, Norbert; Polgari, Zsofia; Mihucz, Victor G.; Zaray, Gyula

2009-01-01

This review is focused on the application of total reflection X-ray fluorescence (TXRF) spectrometry in the field of biological research. In the last decade, most papers were published by authors who applied laboratory-scale TXRF equipments. The application of synchrotron radiation as excitation source (SR-TXRF) shows a slowly increasing tendency. In the cited papers the micro-, trace and multielement capability of these TXRF techniques was demonstrated in the clinical and medical laboratory practice, as well as in various plant physiological studies. For speciation of elements in biological matrices, the TXRF was used as element specific detector following an off-line separation step (e.g., thin layer chromatography, high performance liquid chromatography), however, these off-line methods are not competitive with the on-line coupled HPLC-inductively coupled plasma mass spectrometry

Applicability study of using in-situ gamma-ray spectrometry technique for 137Cs and 210Pbex inventories measurement in grassland environments

International Nuclear Information System (INIS)

Li Junjie; Li Yong; Wang Yanglin; Wu Jiansheng

2010-01-01

In-situ measurement of fallout radionuclides 137 Cs and 210 Pb ex has the potential to assess soil erosion and sedimentation rapidly. In this study, inventories of 137 Cs and 210 Pb ex in the soil of Inner Mongolia grassland were measured using an In-situ Object Counting System (ISOCS). The results from the field study indicate that in-situ gamma-ray spectrometry has the following advantages over traditional laboratory measurements: no extra time is required for sample collection, no reference inventories are required, more economic, prompt availability of the results, the ability to average radionuclide inventory over a large area, and high precision.

Some deficiencies and solutions in gamma ray spectrometry

International Nuclear Information System (INIS)

Westmeier, W.

1998-01-01

A number of problems in high-resolution gamma ray spectrometry as well as some deficiencies of existing computer programs for the quantitative evaluation of spectra are discussed and some practical solutions are proposed. (author)

A simple method for the deconvolution of 134 Cs/137 Cs peaks in gamma-ray scintillation spectrometry

International Nuclear Information System (INIS)

Darko, E.O.; Osae, E.K.; Schandorf, C.

1998-01-01

A simple method for the deconvolution of 134 Cs / 137 Cs peaks in a given mixture of 134 Cs and 137 Cs using Nal(TI) gamma-ray scintillation spectrometry is described. In this method the 795 keV energy of 134 Cs is used as a reference peak to calculate the activity of the 137 Cs directly from the measured peaks. Certified reference materials were measured using the method and compared with a high resolution gamma-ray spectrometry measurements. The results showed good agreement with the certified values. The method is very simple and does not need any complicated mathematics and computer programme to de- convolute the overlapping 604.7 keV and 661.6 keV peaks of 134 Cs and 137 Cs respectively. (author). 14 refs.; 1 tab., 2 figs

X-ray fluorescence spectrometry - an introduction course

International Nuclear Information System (INIS)

Salvador, V.L.R.

1989-01-01

The theoretical and experimental principles of the X-ray fluorescence spectrometry, is presented the text is a synthesis of the most important literature in this area. The authors included are: E.P. Bertin, R. Jenkins, J.L. Devries, R. Muller, R. Tertian, F. Claisse e K.L. Willians. (author)

Certification of reference materials by energy-dispersive x-ray fluorescence spectrometry?

DEFF Research Database (Denmark)

Christensen, Leif Højslet; Heydorn, Kaj

1985-01-01

This paper studies the precision and accuracy that can be achieved using energy-dispersive x-ray fluorescence spectrometry for the determination of total sulphur content in BCR 38 Fly Ash issued by the European Community Bureau of Reference.......This paper studies the precision and accuracy that can be achieved using energy-dispersive x-ray fluorescence spectrometry for the determination of total sulphur content in BCR 38 Fly Ash issued by the European Community Bureau of Reference....

Airborne gamma-ray spectrometry data processing using 1.5D inversion.

Science.gov (United States)

Druker, Eugene

2017-10-01

Standard processing of Airborne Gamma-Ray Spectrometry data generally gives good results when the measurement conditions are almost constant within several footprint area sizes, with the possible exception of flight height variations in a small range. In practice, deviations, such as large or abrupt changes of flight height and/or rugged terrain are not so rare and lead to certain problems. This article proposes a different approach where the solutions of inverse problems are used for data processing. The approach is quite natural in the processing of field data measured along the flight lines: it explicitly takes into account 1.5D survey models and flight parameters - from topography to sources distribution on the surface. Also, it clearly demonstrates that the inverse problem of the Airborne Gamma-Ray Spectrometry does not have a unique solution. This feature can be used in accordance with the underlying geological problem since various formulations of inverse problems can lead to various geological solutions. The use of the approach is illustrated by several examples given for flight lines and survey areas. This approach can be particularly useful in situations where geological, geophysical and/or geographic survey conditions are far from the standard assumptions. Copyright © 2017 Elsevier Ltd. All rights reserved.

The application of X-ray fluorescence spectrometry to prospecting potential gold deposits

International Nuclear Information System (INIS)

Shang Fengjun; Wang Haixia; Zhou Rongsheng

2001-01-01

The fieldwork high-sensitivity X-ray fluorescence analysis (FXFA) adopting miniaturized X-ray tube, Si-PIN detector with peltier cooler and notebook PC spectrometry is presented. Using this system, the authors carried out a preliminary research of its application to some gold mine in Sichuan. According to the close relationship between the high-grade element arsenic and gold in ore-forming components, X-ray fluorescence spectrometry can be used to reveal the existence of potential gold mineralization in fields rapidly. This is of great significance in guiding the field geological collection

Advanced β-ray-induced X-ray spectrometry for non-destructive measurement of tritium retained in fusion related materials

Energy Technology Data Exchange (ETDEWEB)

Matsuyama, Masao, E-mail: matsu3h@ctg.u-toyama.ac.jp; Abe, Shinsuke

2016-11-01

Highlights: • A new measurement system to measure low-Z elements such as C and O atoms has been constructed for evaluation of tritium trapped by these elements. - Abstract: A new β-ray-induced X-ray measurement system equipped with a silicon drift detector, which was named “Advanced-BIXS”, was constructed to study in detail retention behavior of surface tritium by measurements of low energy X-rays below 1 keV such as C(K{sub α}) and O(K{sub α}) as well as high energy X-rays induced by β-rays from tritium. In this study, basic performance of the present system has been examined using various tritium-containing samples. It was seen that energy linearity, energy resolution and sensitivity were quite enough for measurements of low energy X-rays induced by β-rays. Intensity of characteristic X-rays emitted from the surface and/or bulk of a tritium-containing sample was lowered by argon used as a working gas of the Advanced-BIXS. Pressure dependence of transmittance of C(K{sub α}) and Fe(K{sub α}) was examined as examples of low and high energy X-rays, and it was able to represent by using the mass absorption coefficient in argon. It was concluded, therefore, that the present system has high potentiality for nondestructive measurements of tritium retained in surface layers and/or bulk of fusion related materials.

Physical methods for studying minerals and solid materials: X-ray, electron and neutron diffraction; scanning and transmission electron microscopy; X-ray, electron and ion spectrometry

International Nuclear Information System (INIS)

Eberhart, J.-P.

1976-01-01

The following topics are discussed: theoretical aspects of radiation-matter interactions; production and measurement of radiations (X rays, electrons, neutrons); applications of radiation interactions to the study of crystalline materials. The following techniques are presented: X-ray and neutron diffraction, electron microscopy, electron diffraction, X-ray fluorescence analysis, electron probe microanalysis, surface analysis by electron emission spectrometry (ESCA and Auger electrons), scanning electron microscopy, secondary ion emission analysis [fr

Assessment of coal and ash environmental impact with the use of gamma- and X-ray spectrometry

International Nuclear Information System (INIS)

Kierzek, J.; Malozewska-Bucko, B.; Bukowski, P.; Parus, J.L.; Ciurapisnki, A.; Zaras, S.; Kunach, B.; Wiland, K.

1999-01-01

Gamma-ray spectrometry (GS), energy dispersive X-ray fluorescence (EDXRF) analysis methods and wavelength dispersive X-ray fluorescence (WDXRF) were applied for the studies of some coal components, e.g., sulphur, light and heavy metal element concentrations and naturally occurring radioactive isotope contents. Hundred fifty coal samples originating mostly from eight different coal mines from Upper Silesian Coal Basin and 150 samples of ash obtained from these coal samples in laboratory by total combustion at final temperature of 820 deg C, were analyzed. Such comparative analyses can be helpful in selection of most suitable kind of coal for burning in electrical power and heat plants to minimize the environmental pollution. (author)

Determination of rare-earth elements in rocks by isotope-excited X-ray fluorescence spectrometry

DEFF Research Database (Denmark)

Kunzendorf, Helmar; Wollenberg, H.A.

1970-01-01

Isotope-excited X-ray fluorescence spectrometry furnishes a rapid determination of rare-earth elements in unprepared rock samples. The samples are excited by 241Am γ-rays, generating X-ray spectra on a multichannel pulse-height analyser. Gaussian peaks of the Kα and Kβ X-ray energies are treated ......-ray spectrometric scan of a longitudinally sliced drill core showed a close correlation between rare-earth abundances and appropriate minerals.......Isotope-excited X-ray fluorescence spectrometry furnishes a rapid determination of rare-earth elements in unprepared rock samples. The samples are excited by 241Am γ-rays, generating X-ray spectra on a multichannel pulse-height analyser. Gaussian peaks of the Kα and Kβ X-ray energies are treated...

Investigation by gamma-ray spectrometry and INAA of radioactivity impact on phosphate fertilizer plant environment

International Nuclear Information System (INIS)

Pantelica, A.; Companis, I.; Georgescu, I. I.; Pincovshi, E.

2006-01-01

The radioactive polluting effect of a phosphate fertilizer plant on the environment was investigated by gamma-ray spectrometry and neutron activation analysis (INAA). The hazards could arise from industrial plants using raw phosphate materials to prepare fertilizers for agricultural purposes due to the phosphate rock which, depending on the type and geographical zone of provenance may contain rather large amounts of uranium. The fertilizer plant under study is situated about 4 km from the town of Turnu Magurele, on the left bank of the Danube River in Romania. The main by-products of the factory are: nitro phosphate type fertilizers (NP, NPK), Ammonia, Nitric acid, Ammonium nitrate, Urea, Sulfuric acid, Phosphoric acid, Sodium fluorosilicate and Aluminum sulfate. Gamma-ray spectrometry was used to determine activity concentrations of naturally occurring radionuclides ( 2 26Ra, 2 35U, 2 38U, 2 32Th, and 4 0K), as well as 1 37Cs man-made radionuclide in surface soils collected from semicircular areas within radii of 0.5 and 15 km of the plant; in addition, different NPK type fertilizers and phosphate rocks were investigated. The samples (mass of about 100-g each) were kept tightly closed for one month to permit 2 26Ra to establish radioactive equilibrium with its decay products. This method makes it possible to assess U, Th, and K contents in samples by measuring 2 38U and 2 32Th (in equilibrium with their radioactive daughters) and 4 0K radioactivity, taken into account that 1 g of U, Th and K yield 1 2358 Bq 2 38U, 569 Bq 2 35U, 4057.2 Bq 2 32Th and 33.11 Bq 4 0K, respectively. The spectrometrical chain was based on a HPGe (EG and G Ortec) detector of 30 % relative efficiency and 2.1 keV resolution at 1332 keV of 6 0Co. INAA technique (neutron irradiation at TRIGA reactor of SCN Pitesti) was used to determine macro, micro and trace elements in samples collected from both technological shops of the factory (air dust and drinking tap water) and its surroundings

Determination of trace metals in nuclear-grade uranium dioxide by X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Salvador, V.L.R.; Imakuma, K.

1988-04-01

A method is described for the simultaneous determination of low concentrations of Ca, Cr, Cu, Fe, Mn and Ni in nuclear-grade uranium dioxide by X-ray fluorescence spectrometry, without the use of chemical treatment. The lower limits of detection range from 2 μg g -1 for nickel and manganese to 5 μg g -1 for copper. Samples are prepared in the form of double-layer pellets with boric acid as a binding agent. Standards are prepared in a U 3 O 8 matrix, which is more chemically stable than UO 2 and has similar matrix behaviour. The correlation coefficients for calibration curves are better than 0.999. Erros range from 2.4 % for chromium to 6.8 % for nickel. (author) [pt

Energy dispersive x-ray spectrometry by microcalorimetry for the SEM

CERN Document Server

Newbury, D; Sae Woo Nam; Hilton, G; Irwin, K; Small, J; Martinis, J

2002-01-01

Analytical x-ray spectrometry for electron beam instruments has advanced significantly with the development of the microcalorimeter energy dispersive x-ray spectrometer (mu cal EDS). The mu cal EDS operates by measuring the temperature rise when a single photon is absorbed in a metal target. A cryoelectronic circuit with electrothermal feedback and a superconducting transition edge sensor serves as the thermometer. Spectral resolution approaching 4.5 eV for high energy photons (6000 eV) and 2 eV for low energy photons below 2000 eV has been demonstrated in energy dispersive operation across a photon energy range from 250 eV to 8 keV. Spectra of a variety of materials demonstrate the power of the mu cal EDS to solve practical problems while operating on a scanning electron microscope platform. (author)

Combined X-ray CT and mass spectrometry for biomedical imaging applications

Science.gov (United States)

Schioppa, E., Jr.; Ellis, S.; Bruinen, A. L.; Visser, J.; Heeren, R. M. A.; Uher, J.; Koffeman, E.

2014-04-01

Imaging technologies play a key role in many branches of science, especially in biology and medicine. They provide an invaluable insight into both internal structure and processes within a broad range of samples. There are many techniques that allow one to obtain images of an object. Different techniques are based on the analysis of a particular sample property by means of a dedicated imaging system, and as such, each imaging modality provides the researcher with different information. The use of multimodal imaging (imaging with several different techniques) can provide additional and complementary information that is not possible when employing a single imaging technique alone. In this study, we present for the first time a multi-modal imaging technique where X-ray computerized tomography (CT) is combined with mass spectrometry imaging (MSI). While X-ray CT provides 3-dimensional information regarding the internal structure of the sample based on X-ray absorption coefficients, MSI of thin sections acquired from the same sample allows the spatial distribution of many elements/molecules, each distinguished by its unique mass-to-charge ratio (m/z), to be determined within a single measurement and with a spatial resolution as low as 1 μm or even less. The aim of the work is to demonstrate how molecular information from MSI can be spatially correlated with 3D structural information acquired from X-ray CT. In these experiments, frozen samples are imaged in an X-ray CT setup using Medipix based detectors equipped with a CO2 cooled sample holder. Single projections are pre-processed before tomographic reconstruction using a signal-to-thickness calibration. In the second step, the object is sliced into thin sections (circa 20 μm) that are then imaged using both matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) and secondary ion (SIMS) mass spectrometry, where the spatial distribution of specific molecules within the sample is determined. The

Continuous gamma-ray spectrometry in the fast flux test facility (FFTF)

International Nuclear Information System (INIS)

Gold, R.; Kaiser, B.J.; Moore, F.S. Jr.; Bunch, W.L.; McElroy, W.N.; Sheen, E.M.

1980-03-01

In-core Compton-recoil γ-ray spectrometry was carried out in FFTF at very low power in the In-Reactor Thimble (IRT). The lower-energy electron spectrum at the FFTF-IRT midplane and the unfolded γ-ray spectrum are shown. 2 figures

X-ray spectrometry

International Nuclear Information System (INIS)

Markowicz, A.A.; Van Grieken, R.E.

1986-01-01

In the period under review, i.e, through 1984 and 1985, some 600 articles on XRS (X-ray spectrometry) were published; most of these have been scanned and the most fundamental ones are discussed. All references will refer to English-language articles, unless states otherwise. Also general books have appeared on quantitative EPXMA (electron-probe X-ray microanalysis) and analytical electron microscopy (AEM) as well as an extensive review on the application of XRS to trace analysis of environmental samples. In the period under review no radically new developments have been seen in XRS. However, significant improvements have been made. Gain in intensities has been achieved by more efficient excitation, higher reflectivity of dispersing media, and better geometry. Better understanding of the physical process of photon- and electron-specimen interactions led to complex but more accurate equations for correction of various interelement effects. Extensive use of micro- and minicomputers now enables fully automatic operation, including qualitative analysis. However, sample preparation and presentation still put a limit to further progress. Although some authors find XRS in the phase of stabilization or even stagnation, further gradual developments are expected, particularly toward more dedicated equipment, advanced automation, and image analysis systems. Ways are outlined in which XRS has been improved in the 2 last years by excitation, detection, instrumental, methodological, and theoretical advances. 340 references

Installation for β- and X-ray spectrometry

International Nuclear Information System (INIS)

Sokolov, A.D.; Pchelintsev, A.B.; Lupilov, A.V.; Zalinkevich, V.A.; Lapenas, A.

2002-01-01

Paper presents design and parameters of an installation for spectrometry of β- particles and conversion electrons within 15-3000 keV energy range and for X-ray radiation within 2-60 keV range. Si(Li) detector with 500 mm 2 area and 4.5 mm sensitive range thickness is used to record radiation. Energy resolution for 624 keV energy conversion electrons constitutes [ru

Assembly of positioner of automated two-dimensional scan coupled to X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Silva, Leonardo Santiago Melgaço

2011-01-01

This work describes the design and assembling of a prototype automated positioner two-dimensional scanning coupled to X-ray fluorescence spectrometry. The work aims to achieve a portable and easy to use, device of broad utility in the analysis of samples by X-ray fluorescence area of expertise and research. The two-dimensional scanning of the positioner is by means of two stepper motors controlled by a microcontroller PIC 16F877A, encoder and optical sensors. The user interacts with the XY table through an interface program for the Windows operating system, which communicates with the microcontroller through the serial port. The system of Fluorescence Spectroscopy incorporated into the positioner consists of a system commercially available system from the company AMPTEK, where the primary source of excitation of the sample was a source of 241 Am of 59.5 KeV emissions. Resolution and accuracy of tests were performed in the XY scanning process and reproducibility of the same kit with the fluorescence spectrometry X-ray. Qualitative tests by X-ray fluorescence spectrometry in samples were performed to demonstrate the applicability and versatility of the project. It follows that the prototype illustrates a possible adequately to portable device for X-ray spectrometry of two-dimensional. (author)

Analysis of eight argonne premium coal samples by X-ray fluorescence spectrometry

Science.gov (United States)

Evans, J.R.; Sellers, G.A.; Johnson, R.G.; Vivit, D.V.; Kent, J.

1990-01-01

X-ray fluorescence spectrometric methods were used in the analysis of eight Argonne Premium Coal Samples. Trace elements (Cr, Ni, Cu, Zn, Rb, Sr, Y, Zr, Nb, Ba, La, and Ce) in coal ash were determined by energy-dispersive X-ray fluorescence spectrometry; major elements (Na, Mg, Al, Si, P, S, K, Ca, Ti, Mn, and Fe) in coal ash and trace elements (Cl and P) in whole coal were determined by wavelength-dispersive X-ray fluorescence spectrometry. The results of this study will be used in a geochemical database compiled for these materials from various analytical techniques. The experimental XRF methods and procedures used to determine these major and trace elements are described.

Design of a tritium gas cell for beta-ray induced X-ray spectrometry using Monte Carlo simulation

Energy Technology Data Exchange (ETDEWEB)

Hara, Masanori, E-mail: masahara@ctg.u-toyama.ac.jp [Hydrogen Isotope Research Center, Organization for Promotion of Research, University of Toyama, 3190 Gofuku, Toyama City, Toyama 930-8555 (Japan); Abe, Shinsuke; Matsuyama, Masao [Hydrogen Isotope Research Center, Organization for Promotion of Research, University of Toyama, 3190 Gofuku, Toyama City, Toyama 930-8555 (Japan); Aso, Tsukasa [Electronics and Computer Engineering, National Institute of Technology, Toyama College, 1-2 Ebie-neriya, Imizu City, Toyama 933-0293 (Japan); Tatenuma, Katsuyoshi; Kawakami, Tomohiko; Ito, Takeshi [KAKEN Company Limited, 1044 Horimachi, Mito City, Ibaraki 310-0903 (Japan)

2017-06-15

Highlights: • Beta-ray induced X-ray spectrometry (BIXS) is a method for tritium gas analysis. • Gas cell for BIXS was designed by Monte Carlo simulations. • The optimum thickness of the gold layer on a beryllium window was around 150 nm. • This simulation model considered the self-absorption with increasing the cell length. - Abstract: One of the methods used for tritium gas analysis is beta-ray induced X-ray spectrometry (BIXS). Gas cell design is important in this method. The structure of the gas cell for BIXS was optimized by Monte Carlo simulation of beta-ray induced X-ray spectra in various window geometries using the Geant4 tool kit (version 10.01.p02). The simulated spectrum from tritium decay fitted the observed one, and the simulation model was used to obtain the cell parameters for BIXS. The optimum thickness of the gold layer on a beryllium window was around 150 nm. This simulation model also considered the relationship between self-absorption by hydrogen gas and the cell length. Self-absorption increased with increasing cell length and the relationship between the sample pressure and cell length was formulated.

Target characterization by PIXE, alpha spectrometry and X-ray absorption

International Nuclear Information System (INIS)

Kheswa, N.Y.; Papka, P.; Pineda-Vargas, C.A.; Newman, R.T.

2011-01-01

We report on the thickness and homogeneity characterization of thin metallic targets of Zr-96 by means of alpha absorption spectrometry, Particle Induced X-ray Emission (PIXE) and X-ray absorption. The target thicknesses determined by means of the above mentioned methods are critically compared. The thicknesses were determined before and after irradiation with a 70 MeV beam of 14 N ions.

Measurement of radon concentration in ground water at Saijo sake brewery by means of γ-ray spectrometry

International Nuclear Information System (INIS)

Takenaka, Kodai; Takatori, Hiroshi; Kojima, Yasuaki; Shizuma, Kiyoshi

2008-01-01

Recently, natural water such as ground water and/or spring water of various places is popular for the environmental preservation and safety of food. Measurement of the radon concentration in ground water is important for risk estimate of drinking water and whether the water can be authorized as the mineral spring (74 Bq/L). In this work, radon concentration is ground water from eight places which were utilized for Saijo sake breweries was measured by means of γ-ray spectrometry. Radon concentration in each well was measured every month for two years. The variation in the radon concentration was investigated for seasonal variation, difference between the type of well, correlations with pH, water temperature and atmospheric temperature. The results are as follows: An average value of the radon concentration was 160 Bq/L which meant most of ground water satisfies the mineral spring standard. The radon concentration of the drilling well was higher than that of the punched well. The variation in the radon concentration shows no seasonal variations, nor depends on the water temperature, the atmospheric temperature and the pH. (author)

Efficiency curves of NIRR-1 gamma-ray spectrometry system at near ...

African Journals Online (AJOL)

The full-energy peak efficiency curves of the gamma-ray spectrometry for use with the Nigeria Research Reactor-1 (NIRR-1) have been determined by both theoretical and experimental at two source-detector positions for routine neutron activation analysis. Standard gamma ray sources were used to determine the efficiency ...

X-ray fluorescence spectrometry applied to soil analysis

International Nuclear Information System (INIS)

Salvador, Vera Lucia Ribeiro; Sato, Ivone Mulako; Scapin Junior, Wilson Santo; Scapin, Marcos Antonio; Imakima, Kengo

1997-01-01

This paper studies the X-ray fluorescence spectrometry applied to the soil analysis. A comparative study of the WD-XRFS and ED-XRFS techniques was carried out by using the following soil samples: SL-1, SOIL-7 and marine sediment SD-M-2/TM, from IAEA, and clay, JG-1a from Geological Survey of Japan (GSJ)

A simple source preparation method for alpha-ray spectrometry of volcanic rock sample

International Nuclear Information System (INIS)

Takahashi, Masaomi; Kurihara, Yuichi; Sato, Jun

2006-01-01

A simple source preparation method was developed for the alpha-ray spectrometry to determine U and Th in volcanic rockes. Isolation of U and Th from volcanic rocks was made by use of UTEVA-Spec. resin, extraction chromatograph material. U and Th were extracted by TTA-benzene solution and organic phase was evaporated drop by drop on a hot stainless steel planchet to dryness. This method was found to be effective for the preparation of sources for alpha-ray spectrometry. (author)

Natural gamma-ray spectrometry as a tool for radiation dose and radon hazard modelling

International Nuclear Information System (INIS)

Verdoya, M.; Chiozzi, P.; De Felice, P.; Pasquale, V.; Bochiolo, M.; Genovesi, I.

2009-01-01

We reviewed the calibration procedures of gamma-ray spectrometry with particular emphasis to factors that affect accuracy, detection limits and background radiation in field measurements for dosimetric and radon potential mapping. Gamma-ray spectra were acquired in western Liguria (Italy). The energy windows investigated are centred on the photopeaks of 214 Bi (1.76 MeV), 208 Tl (2.62 MeV) and 40 K (1.46 MeV). The inferred absorbed dose rate and the radon flux are estimated to be lower than 60 nGy h -1 and 22 Bq m -2 h -1 , respectively.

Fricke dosimetry: the difference between G(Fe3+) for 60Co gamma-rays and high-energy x-rays.

Science.gov (United States)

Klassen, N V; Shortt, K R; Seuntjens, J; Ross, C K

1999-07-01

A calibration of the Fricke dosimeter is a measurement of epsilon G(Fe3+). Although G(Fe3+) is expected to be approximately energy independent for all low-LET radiation, existing data are not adequate to rule out the possibility of changes of a few per cent with beam quality. When a high-precision Fricke dosimeter, which has been calibrated for one particular low-LET beam quality, is used to measure the absorbed dose for another low-LET beam quality, the accuracy of the absorbed dose measurement is limited by the uncertainty in the value of G(Fe3+). The ratio of G(Fe3+) for high-energy x-rays (20 and 30 MV) to G(Fe3+) for 60Co gamma-rays, G(Fe3+)MV(Co), was measured to be 1.007(+/-0.003) (confidence level of 68%) using two different types of water calorimeter, a stirred-water calorimeter (20 MV) and a sealed-water calorimeter (20, 30 MV). This value is consistent with our calculations based on the LET dependence of G(primary products) and, as well, with published measurements and theoretical treatments of G(Fe3+).

Application of neutron activation techniques and x-ray energy dispersion spectrometry, in analysis of metallic traces adsorbed by chelex-100 resin

International Nuclear Information System (INIS)

Fernandes, Jair C.; Amaral, Angela M.; Magalhaes, Jesus C.; Pereira, Jose S.J.; Silva, Juliana B. da; Auler, Lucia M.L.A.

2000-01-01

In this work, the authors have investigated optimal conditions of adsorption for several ion metallic groups (cations of heavy metals and transition metals, oxyanions metallics and metalloids and cations of rare earths), as traces (ppb), withdrawn and in mixture of groups, by chelex-100 resin. The experiments have been developed by bath techniques in ammonium acetate tamponade solution 40 mM pH 5,52 content 0,5 g of chelex-100 resin. After magnetic agitation for two hours, resins were dried and submitted to X-ray energy dispersion spectrometry, x-ray fluorescence spectrometry and neutron activation analysis. The results have demonstrated that chelex-100 resin adsorb quantitatively transition element groups and rare earth groups in two cases (withdrawn and simultaneously adsorption)

Evaluation of a new optic-enabled portable X-ray fluorescence spectrometry instrument for measuring toxic metals/metalloids in consumer goods and cultural products

Science.gov (United States)

Guimarães, Diana; Praamsma, Meredith L.; Parsons, Patrick J.

2016-08-01

X-ray fluorescence spectrometry (XRF) is a rapid, non-destructive multi-elemental analytical technique used for determining elemental contents ranging from percent down to the μg/g level. Although detection limits are much higher for XRF compared to other laboratory-based methods, such as inductively coupled plasma mass spectrometry (ICP-MS), ICP-optical emission spectrometry (OES) and atomic absorption spectrometry (AAS), its portability and ease of use make it a valuable tool, especially for field-based studies. A growing necessity to monitor human exposure to toxic metals and metalloids in consumer goods, cultural products, foods and other sample types while performing the analysis in situ has led to several important developments in portable XRF technology. In this study, a new portable XRF analyzer based on the use of doubly curved crystal optics (HD Mobile®) was evaluated for detecting toxic elements in foods, medicines, cosmetics and spices used in many Asian communities. Two models of the HD Mobile® (a pre-production and a final production unit) were investigated. Performance parameters including accuracy, precision and detection limits were characterized in a laboratory setting using certified reference materials (CRMs) and standard solutions. Bias estimates for key elements of public health significance such as As, Cd, Hg and Pb ranged from - 10% to 11% for the pre-production, and - 14% to 16% for the final production model. Five archived public health samples including herbal medicine products, ethnic spices and cosmetic products were analyzed using both XRF instruments. There was good agreement between the pre-production and final production models for the four key elements, such that the data were judged to be fit-for-purpose for the majority of samples analyzed. Detection of the four key elements of interest using the HD Mobile® was confirmed using archived samples for which ICP-OES data were available based on digested sample materials. The HD

Comparative and Absolute Measurements of 11 Inorganic Constituents of 38 Human Tooth Samples with Gamma-ray Spectrometry

Energy Technology Data Exchange (ETDEWEB)

Samsahl, K [AB Atomenergi, Stockholm (Sweden); Soeremark, R [The Clinical Laboratory and the Dept. of Prosthetics of the Royal School of Dentistry, Stockholm (Sweden)

1961-12-15

The mean concentrations of the following elements have been simultaneously determined in normal human dentine, enamel and dental calculus with gamma-ray spectrometry; Na, P, Cl, Ca, Mn, Cu, Zn, Br, Sr, W and Au. In a typical run one sample each of dentine, enamel and dental calculus were irradiated together with standards of the elements to be determined in a thermal neutron flux of 2 x 10{sup 12} n/cm/sec for 20 hours. The chemical elements were separated into nine groups with ion exchange technique before the subsequent gamma spectrometric measurements. One man can manage the chemical separations and take the necessary gamma spectra from a run in one day. In a few samples of dentine, enamel and dental calculus which had been irradiated in a thermal neutron flux of 7 x 10{sup 13} n/cm/sec for one week the additional long lived trace elements were qualitatively determined Cr, Fe, Co, Rb, Ag, Sb, Cs and Ba.

Comparative and Absolute Measurements of 11 Inorganic Constituents of 38 Human Tooth Samples with Gamma-ray Spectrometry

International Nuclear Information System (INIS)

Samsahl, K.; Soeremark, R.

1961-12-01

The mean concentrations of the following elements have been simultaneously determined in normal human dentine, enamel and dental calculus with gamma-ray spectrometry; Na, P, Cl, Ca, Mn, Cu, Zn, Br, Sr, W and Au. In a typical run one sample each of dentine, enamel and dental calculus were irradiated together with standards of the elements to be determined in a thermal neutron flux of 2 x 10 12 n/cm/sec for 20 hours. The chemical elements were separated into nine groups with ion exchange technique before the subsequent gamma spectrometric measurements. One man can manage the chemical separations and take the necessary gamma spectra from a run in one day. In a few samples of dentine, enamel and dental calculus which had been irradiated in a thermal neutron flux of 7 x 10 13 n/cm/sec for one week the additional long lived trace elements were qualitatively determined Cr, Fe, Co, Rb, Ag, Sb, Cs and Ba

Survey of natural radioactivity levels in Ilex paraguariensis (St. Hil.) by gamma-ray spectrometry

International Nuclear Information System (INIS)

Scheibel, Viviane; Appoloni, Carlos Roberto

2007-01-01

The mate tea (Ilex paraguariensis - St. Hil.) is a beverage broadly cultivated and consumed in Brazil. The radioactive traces present in three trademarks of toasted mate tea produced at the south of Brazil were analyzed. Measurements were carried out by gamma-ray spectrometry. The average value for the 40 K activity measured for marks A, B and C was 1216 ± 8, 1047 ± 14 and 666 ± 13 Bq.kg -1 , respectively. The 137 Cs activity was lower than the limit of detection. (author)

X-ray spectrometry induced by electron and proton bombardment: Two complementary techniques for the micro-characterization of mineral materials

International Nuclear Information System (INIS)

Remond, G.; Gilles, C.; Isabelle, D.; Choi, C.G.; Rouer, O.; Cesbron, F.; Yang, C.

1994-01-01

Spatially resolved quantitative analysis by means of the Electron Probe Micro Analyser (EPMA) is now well established as a routine analytical method for point chemical analysis of a variety of mineral materials. Modern computer controlled EPMA are most often equipped with wavelength dispersive spectro- meters (WDS). Quantitative analyses are generally carried out according to a standard based approach, i. e, the x-ray intensities measured at the surface of the unknowns are normalized to those measured at the surface of reference specimens. By the use of energy dispersive spectrometry (EDS) a standardless quantitative based method is preferred when the incident beam current is not accurately known as for the case of EDS analysis coupled to Scanning Electron Microscopy (SEM). The accuracy of point analysis by means of electron beam induced x-ray spectrometry is discussed emphasizing the x-ray photon interactions respectively.The continuous x-ray emission is the physical limit of detection. The excitation conditions must be optimised in order to obtain the higher peak to continuous emission intensity ratios for each element within the matrix. Proton Induced X-ray Emission (PIXE) complements this electron induced x-ray emission for the localization of elements present at trace levels. The experimental procedure used for quantitative analysis by means of PIXE is illustrated emphasizing the use of a limited number of reference materials for deriving quantitative data from the raw PIXE spectra. The complementarity of EMPA/SEM and PIXE techniques is illustrated for the case of rare-earth elements (REE) bearing natural and synthetic doped zircon crystals (Si Zr O sub 4). For such compounds x-ray spectra are very complex because of the existence of severe peak overlaps between the L x-ray emission spectra of the REE. It is shown that cathodoluminescence (EPLA:SEM) and ionoluminescence (PIXE) may be an original alternative approach to x-ray spectrometry for studying REE

Application of total reflection X-ray fluorescence spectrometry for ...

Indian Academy of Sciences (India)

Applicability of total reflection X-ray fluorescence (TXRF) spectrometry for trace elemental analysis of rainwater samples was studied. The study was used to develop these samples as rainwater standards by the National University of Singapore (NUS). Our laboratory was one of the participants to use TXRF for this study.

Angle-resolved X-ray fluorescence spectrometry using synchrotron radiation at ELSA

International Nuclear Information System (INIS)

Schmitt, W.; Rothe, J.; Hormes, J.; Gries, W.H.

1994-01-01

Measurements on the centroid depth of ion-implanted phosphorus-in-silicon specimen by the method of angle-resolved, self-ratio X-ray fluorescence spectrometry (AR/SR/XFS) have been carried out using 'white' synchrotron radiation (SR). The measurements were performed using a modified wavelength-dispersive fluorescence spectrometer. Problems due to the use of SR, like carbonaceous specimen contamination and sample heating were overcome by flooding the specimen chamber with helium and by pre-absorbing the non-exciting parts of the incident SR with suitable filters, respectively. The decaying primary intensity was monitored by measuring the compensation current of the photoelectrons emitted from a tungsten wire stretched across the primary beam. Results have been obtained for specimen with dose density levels of 10 16 cm -2 and 3x10 15 cm -2 . (orig.)

The determination, by x-ray-fluorescence spectrometry, of gold, silver, and base metals on activated carbon

International Nuclear Information System (INIS)

Wall, G.; Jacobs, J.J.; Dixon, K.

1980-01-01

The method proposed involves ashing of the sample at a low temperature in a muffle furnace, mixing of the ash with alumina and boric acid in a Siebtechnik mill, and briquetting of the mixture. The elements are measured in the briquette by the use of x-ray fluorescence spectrometry. The detailed laboratory method is given in an appendix [af

Method for detecting binding events using micro-X-ray fluorescence spectrometry

Science.gov (United States)

Warner, Benjamin P.; Havrilla, George J.; Mann, Grace

2010-12-28

Method for detecting binding events using micro-X-ray fluorescence spectrometry. Receptors are exposed to at least one potential binder and arrayed on a substrate support. Each member of the array is exposed to X-ray radiation. The magnitude of a detectable X-ray fluorescence signal for at least one element can be used to determine whether a binding event between a binder and a receptor has occurred, and can provide information related to the extent of binding between the binder and receptor.

Determination of vanadium in titanate-based ferroelectrics by INAA with discriminating gamma-ray spectrometry

Czech Academy of Sciences Publication Activity Database

Kameník, Jan; Dragounová, K.; Kučera, Jan; Bryknar, Z.; Trepakov, Vladimír; Strunga, Vladimír

2017-01-01

Roč. 311, č. 2 (2017), s. 1333-1338 ISSN 0236-5731. [1st International Conference on Radioanalytical and Nuclear chemistry (RANC). Budapest, 10.04.2016-15.04.2016] R&D Projects: GA ČR(CZ) GBP108/12/G108; GA MŠk LM2015056 Institutional support: RVO:68378271 ; RVO:61389005 Keywords : Titanate-based ferroelectrics * Vanadium * INAA * discriminating gamma-ray spectrometry Subject RIV: CB - Analytical Chemistry, Separation; BM - Solid Matter Physics ; Magnetism (FZU-D) OBOR OECD: Analytical chemistry; Condensed matter physics (including formerly solid state physics, supercond.) (FZU-D) Impact factor: 1.282, year: 2016

Gamma-ray measurements for uranium enrichment standards

International Nuclear Information System (INIS)

Reilly, T.D.

1979-01-01

The gamma-ray spectroscopic measurement of uranium enrichment is one of the most widely used nondestructive analysis techniques. A study has been started of the precision and accuracy achievable with this technique and the physical parameters which affect it. The study was prompted by questions raised during the ongoing ESARDA-NBS experiment to produce uranium oxide reference counting materials for the technique. Results reported using a high-quality Ge(Li) spectrometer system show reproducibility comparable to that attainable with mass spectrometry

Cu,Cr and As determination in preserved woods (Eucalyptus ssp.) by X-ray fluorescence spectrometries

International Nuclear Information System (INIS)

Pereira Junior, Sergio Matias

2014-01-01

Brazil produces around 2.2 millions of cubic meters of treated wood to meet the annual demand of railway, electric, rural and construction sectors. The most used wood species are eucalyptus (Eucalyptus ssp.) and pine (Pinus ssp.).The treated woods used for poles, sleepers, fence posts and plywoods should be according to Brazilian norms requirements. The most usual wood preservative products used in Brazil are CCA (chromated copper arsenate) and CCB (copper chromium and boron salt). The analytical methods, such as flame atomic absorption spectrometry (FAAS), plasma inductively coupled optical emission spectrometry (ICPOES) and X-ray fluorescence spectrometry (XRFS) have been used for the analytical control of those treatment processes. In this work, the eucalyptus trees (Eucalyptus ssp) samples was obtained from Minas Gerais State, Brazil, cut plantation areas. Under pressure, eucalyptus wood samples were submitted to different concentration of CCA solution reaching 3.9, 6.7, 9.1, 12.4 and 14.0 kg of CCA by m-³ sapwood retentions. Samples in cylinders and sawdust forms were obtained from treated wood samples. Copper, chromium and arsenic determination was performed using the energy dispersive X-ray fluorescence spectrometry (EDXRFS), portable X-ray fluorescence spectrometry (PXRFS), flame atomic absorption spectrometry (FAAS) and instrumental neutron activation analysis. In this work, the method of analysis, sensitivity, precision and accuracy performances of the related techniques were outlined. (author)

γ-Ray spectrometry of radon in water and the role of radon to representatively sample aquifers

International Nuclear Information System (INIS)

Talha, S.A.; Lindsay, R.; Newman, R.T.; Meijer, R.J. de; Maleka, P.P.; Hlatshwayo, I.N.; Mlwilo, N.A.; Mohanty, A.K.

2008-01-01

Measurement of radon in water by γ-ray spectrometry using a HPGe detector has been investigated to determine aquifer characteristics. The radon activity concentration is determined by taking the weighted average of the concentrations derived from γ-ray lines associated with 214 Pb and 214 Bi decay. The role of accurate radon data to representatively sample aquifers was also investigated by studying a semi-cased borehole. A simplified physical model describing the change of radon concentration with the pumping time, reproduces the data and predicts the time for representative sampling of the aquifer

Experimental determination of nuclear reaction rates (n,γ) by the gamma-rays capture spectrometry technique

International Nuclear Information System (INIS)

Lucatero, M.A.

1976-01-01

The technique of the gamma-rays capture spectrometry was used in the experimental determination of nuclear reaction rates of the type (n,γ). This technique consists in the incidence of a thermal neutrons collimated beam upon a sample, detecting the capture spectrum of gamma rays emitted at a solid fixed angle. In the determination of the efficiency curve intrinsic to the detection electronic system the reactions 199 Hg(n,γ) 200 Hg, 56 Fe(n,γ) 57 Fe and 63 Cu(n,γ) 64 Cu were used with the energy of the gamma rays capture of 5.976, 7.635 and 7.915 Mev respectively, through the irradiation of standard samples of Hg(175.3g), Fe(110.4g) and Cu(108.5g) of cylindrical geometry the two former and parallelepiped the latter. The problem concerning the corrections due to the thermal neutrons flux depression, the gammas auto-attenuation, and the geometric factor due to the cylindrical and parallelepiped geometry are involved in the data process. The experimental determination of the reaction 35 Cl(n,γ) 36 Cl rate was made through the observation of the gamma caputre of 6.111 Mev when a sample of CaCl 2 of cylindrical geometry was irradiated. This rate can be favorably compared with the reaction rate determined theoretically. (author)

In-situ-gamma ray spectrometry for measurements of environmental radioactivity

Energy Technology Data Exchange (ETDEWEB)

Winkelmann, I

1994-12-31

A detailed description of the method is presented. The range of application is shown. The calibration of the in-situ gamma ray spectrometer with a HPGe semiconductor detector and the evaluation of the spectra are described. A measuring time of about 15-30 min is sufficient to determine the specific natural and man-made radioactivity of the soil of some ten Bq/m{sup 2}. The results of soil contamination measurements in Germany after the Chernobyl accident are reported. A total of 22 nuclides are detected. The measured contamination for the first days after the accident was as follows: {sup 132}Te/{sup 132}I - 100 kBq/m{sup 2}, and {sup 131}I - 70 kBq/m{sup 2}. 6 figs., 4 tabs. (orig.).

X-ray dosimetry in mammography for W/Mo and Mo/Mo combinations utilizing Compton spectrometry

International Nuclear Information System (INIS)

Almeida Junior, Jose N.; Terini, Ricardo A.; Herdade, Silvio B.; Furquim, Tania A.C.

2009-01-01

Mean Glandular Dose (MGD) cannot be measured directly in mammography equipment. Therefore, methods based on Compton spectrometry are alternatives to evaluate dose distributions in a standard breast phantom, as well as mean glandular dose. In this work, a CdTe detector was used for the spectrometry measurements of radiation scattered by compton effect, at nearly 90, by a PMMA cylinder. For this, the reconstruction of primary beam spectra from the scattered ones has been made using Klein-Nishina theory and Compton formalism, followed by a determination of incident air kerma, absorbed dose values in the breast phantom and, finally, MGD. Incident and attenuated X-ray spectra and depth-dose distributions in a BR-12 phantom have been determined and are presented for the mammography range (28 to 35kV), showing good agreement with previous literature data, obtained with TLD. (author)

Ferro-metry and X-ray fluorescence to measure wear

International Nuclear Information System (INIS)

Catherin, J.Y.

1997-01-01

The determination of wear of metallic structures is carried out by measuring metallic particles in the lubricating oil. This method is routinely used by SNCF, the French railroad company to control the motors of the high speed trains (TGV). Four methods, plasma emission spectrometry, X-ray fluorescence analysis, ferro-metry and magnetometry are used. The field of application and advantage of each method is described. (C.B.)

Automatic sample changer system for a chain of X-Ray Spectrometry

International Nuclear Information System (INIS)

Kall, B.

2004-01-01

Nowadays, the science evolves and the used techniques become more pointed. At the same time, instruments are more powerful. This rule also applies in the domain of the nuclear science. The object of these works goes in this sense and touch the branch of the X-Ray spectrometry and that brings back himself to the conception and the realization of an automatic sample changer system for the chain of X-Ray Spectrometry. Baptized KEN-001 , it is an instrument of sample changer ordered from certain distance. Indeed, the sample carriers are placed of advance in compartments on its tray and by a control, KEN-001 put one by one those reflectors in the carries reflective for analysis. Once the analysis is finished, the system is in charge of taking and replacing the reflector in its compartment of origin. Of this way, one wins in time and therefore in number of analysis to do in an interval of time given. This instrument of precision contributes to the improvement of the analysis and the evolution of the technique of the X-Ray fluorescence [fr

The Determination of γ and X Rays Variation in Radioactivity Measurement of Eu-152 Using Merlin Gerin Ionization Chamber

International Nuclear Information System (INIS)

Gatot-Wurdiyanto; Tuti-Budiantari, C; Ermi-Juita; Hermawan-Candra; Eni-Suswantini; Holnisar; Wahyudi

2001-01-01

Activity measurement of Eu-152 was carried out by using dose calibrator Merlin Gerin. Four samples having their solution factors was prepared for the measurement. The activities of each sample were determined with four variations of γ-rays and X-rays, namely all of γ-rays, all of γ rays and all of X-rays; 15 greater γ-rays intensities; 15 greater γ-rays intensities and all of X-rays. The reference of the measurement is the measurement result using γ-spectrometry methods. The result of the measurement is fairly good, meanwhile the best measurement of Eu-152 is based on all of γ-rays and X-rays which its difference of under 0.5 %. (author)

Soft X-ray-induced decomposition of amino acids: An XPS, mass spectrometry, and NEXAFS study

International Nuclear Information System (INIS)

Zubavichus, Yan; Fuchs, Oliver; Weinhardt, Lothar; Heske, Clemens; Umbach, Eberhard; Denlinger, Jonathan D.; Grunze, Michael

2003-01-01

Decomposition of five amino acids, alanine, serine, cysteine, aspartic acid, and asparagine, under irradiation with soft X-rays (magnesium Ka X-ray source) in ultra-high vacuum was studied by means of X-ray photoelectron spectrometry (XPS) and mass spectrometry. A comparative analysis of changes in XPS line shapes, stoichiometry and residual gas composition indicates that the molecules decompose by several pathways. Dehydration, decarboxylation, decarbonylation,deamination and desulfurization of pristine molecules accompanied by desorption of H2, H2O, CO2, CO, NH3and H2S are observed with rates depending on the specific amino acid. NEXAFS spectra of cysteine at the carbon, oxygen and nitrogen K-shell and sulfur L2,3 edges complement the XPS and mass spectrometry data and show that the exposure of the sample to an intense soft X-ray synchrotron beam results in the formation of C-C and C-N double and triple bonds. Qualitatively, the amino acids studied can be arranged in the following ascending order of radiation stability:serine< alanine< aspartic acid< cysteine< asparagine

Forensic application of total reflection X-ray fluorescence spectrometry for elemental characterization of ink samples

International Nuclear Information System (INIS)

Dhara, Sangita; Misra, N.L.; Maind, S.D.; Kumar, Sanjukta A.; Chattopadhyay, N.; Aggarwal, S.K.

2010-01-01

The possibility of applying Total Reflection X-ray Fluorescence for qualitative and quantitative differentiation of documents printed with rare earth tagged and untagged inks has been explored in this paper. For qualitative differentiation, a very small amount of ink was loosened from the printed documents by smoothly rubbing with a new clean blade without destroying the manuscript. 50 μL of Milli-Q water was put on this loose powder, on the manuscript, and was agitated by sucking and releasing the suspension two to three times with the help of a micropipette. The resultant dispersion was deposited on quartz sample support for Total Reflection X-ray Fluorescence measurements. The Total Reflection X-ray Fluorescence spectrum of tagged and untagged inks could be clearly differentiated. In order to see the applicability of Total Reflection X-ray Fluorescence for quantitative determinations of rare earths and also to countercheck such determinations in ink samples, the amounts of rare earth in painted papers with single rare earth tagged inks were determined by digesting the painted paper in HNO 3 /HClO 4 , mixing this solution with the internal standard and recording their Total Reflection X-ray Fluorescence spectra after calibration of the instrument. The results thus obtained were compared with those obtained by Inductively Coupled Plasma Mass Spectrometry and were found in good agreement. The average precision of the Total Reflection X-ray Fluorescence determinations was 5.5% (1σ) and the average deviation of Total Reflection X-ray Fluorescence determined values with that of Inductively Coupled Plasma Mass Spectrometry was 7.3%. These studies have shown that Total Reflection X-ray Fluorescence offers a promising and potential application in forensic work of this nature.

Forensic application of total reflection X-ray fluorescence spectrometry for elemental characterization of ink samples

Energy Technology Data Exchange (ETDEWEB)

Dhara, Sangita [Fuel Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Misra, N.L., E-mail: nlmisra@barc.gov.i [Fuel Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Maind, S.D. [NAA Unit of Central Forensic Science Laboratory Hyderabad at Analytical Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Kumar, Sanjukta A. [Analytical Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Chattopadhyay, N. [NAA Unit of Central Forensic Science Laboratory Hyderabad at Analytical Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Aggarwal, S.K. [Fuel Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India)

2010-02-15

The possibility of applying Total Reflection X-ray Fluorescence for qualitative and quantitative differentiation of documents printed with rare earth tagged and untagged inks has been explored in this paper. For qualitative differentiation, a very small amount of ink was loosened from the printed documents by smoothly rubbing with a new clean blade without destroying the manuscript. 50 muL of Milli-Q water was put on this loose powder, on the manuscript, and was agitated by sucking and releasing the suspension two to three times with the help of a micropipette. The resultant dispersion was deposited on quartz sample support for Total Reflection X-ray Fluorescence measurements. The Total Reflection X-ray Fluorescence spectrum of tagged and untagged inks could be clearly differentiated. In order to see the applicability of Total Reflection X-ray Fluorescence for quantitative determinations of rare earths and also to countercheck such determinations in ink samples, the amounts of rare earth in painted papers with single rare earth tagged inks were determined by digesting the painted paper in HNO{sub 3}/HClO{sub 4}, mixing this solution with the internal standard and recording their Total Reflection X-ray Fluorescence spectra after calibration of the instrument. The results thus obtained were compared with those obtained by Inductively Coupled Plasma Mass Spectrometry and were found in good agreement. The average precision of the Total Reflection X-ray Fluorescence determinations was 5.5% (1sigma) and the average deviation of Total Reflection X-ray Fluorescence determined values with that of Inductively Coupled Plasma Mass Spectrometry was 7.3%. These studies have shown that Total Reflection X-ray Fluorescence offers a promising and potential application in forensic work of this nature.

Determination of rare-earth elements in rocks by isotope-excited X-ray fluorescence spectrometry

DEFF Research Database (Denmark)

Kunzendorf, Helmar; Wollenberg, H.A.

1970-01-01

Isotope-excited X-ray fluorescence spectrometry furnishes a rapid determination of rare-earth elements in unprepared rock samples. The samples are excited by 241Am γ-rays, generating X-ray spectra on a multichannel pulse-height analyser. Gaussian peaks of the Kα and Kβ X-ray energies are treated......-ray spectrometric scan of a longitudinally sliced drill core showed a close correlation between rare-earth abundances and appropriate minerals....

Remarks on the gamma-ray spectrometry for the determination of natural radioisotopes

International Nuclear Information System (INIS)

Kalita, S.; Niewodniczanski, J.

1987-01-01

Semiconductor low-energy gamma ray spectrometry is compared with the routinely used scintillation method (within higher energy range). Measurements of low-energy natural gamma radiation using a semiconductor detector permit the determination of radioactive equilibrium of the uranium series. In this method 238 U ( 234 Th) content is determined by 63 keV, 226 Ra by 186 keV and 214 Pb by 295 keV gamma rays. Using the same results one can calculate a radioactive equilibrium coefficient R, defined as concentration ratio 226 Ra/ 238 U and a 222 Rn emanation ratio E, defined as 1 - 214 Pb/ 226 Ra (concentrations in uranium equivalent units). The relative standard errors for the method are: 10 - 15% in case of radioisotope content and about 18% for R and E determination. 7 refs., 2 figs., 2 tabs. (author)

Reactor gamma spectrometry: status

International Nuclear Information System (INIS)

Gold, R.; Kaiser, B.J.

1979-01-01

Current work is described for Compton Recoil Gamma-Ray Spectrometry including developments in experimental technique as well as recent reactor spectrometry measurements. The current status of the method is described concerning gamma spectromoetry probe design and response characteristics. Emphasis is given to gamma spectrometry work in US LWR and BR programs. Gamma spectrometry in BR environments are outlined by focussing on start-up plans for the Fast Test Reactor (FTR). Gamma spectrometry results are presented for a LWR pressure vessel mockup in the Poolside Critical Assembly (PCA) at Oak Ridge National Laboratory

X-Ray Fluorescence Spectrometry. II. Determination of Uranium in ores

International Nuclear Information System (INIS)

Bermudez Polonio, J.; Crus Castillo, F. de la; Fernandez Cellini, R.

1961-01-01

A method of analysis of uranium in ores by X-ray spectrometry was developed, using the internal standard technique. Strontium was found to be the most suitable internal standard for general use. A Norelco Philips X-ray fluorescent spectrometer was used in this work, equipped with a lithium fluoride crystal acting as a diffraction grating analyzer. The intensity of the uranium-L α 1 spectral line is calculated and related to corresponding strontium-K α spectral line, both detected with a Scintillation Counter. (Author) 31 refs

Radon gamma-ray spectrometry with YAP:Ce scintillator

CERN Document Server

Plastino, W; De Notaristefani, F

2002-01-01

The detection properties of a YAP:Ce scintillator (YAlO sub 3 :Ce crystal) optically coupled to a Hamamatsu H5784 photomultiplier with standard bialkali photocathode have been analyzed. In particular, the application to radon and radon-daughters gamma-ray spectrometry was investigated. The crystal response has been studied under severe extreme conditions to simulate environments of geophysical interest, particularly those found in geothermal and volcanic areas. Tests in water up to a temperature of 100 deg.C and in acids solutions such as HCl (37%), H sub 2 SO sub 4 (48%) and HNO sub 3 (65%) have been performed. The measurements with standard radon sources provided by the National Institute for Metrology of Ionizing Radiations (ENEA) have emphasized the non-hygroscopic properties of the scintillator and a small dependence of the light yield on temperature and HNO sub 3. The data collected in this first step of our research have pointed out that the YAP:Ce scintillator can allow high response stability for rad...

Development of gas ionization chambers with coplanar electrodes for alpha-ray spectrometry

International Nuclear Information System (INIS)

Iwasaki, Kenta; Tanaka, Naomichi; Murakami, Kohei; Hasebe, Nobuyuki; Kusano, Hiroki; Shibamura, Eido; Miyajima, Mitsuhiro

2016-01-01

A large-area alpha-ray spectrometer is required to measure the low level alpha emitters in environmental samples, which may be distributed in the vicinity of nuclear power plants. A gas ionization chamber with a coplanar electrode has attractive features such as with mechanical ruggedness, easy handling, easy fabrication of large electrode, and relatively well-known performance. We have investigated the performance of a gas ionization chamber with a coplanar electrode for alpha-ray spectrometry, particularly in the energy resolution. The present experiment shows that the energy resolution in the full width at half maximum (FWHM) is 129 keV (= 2.7%) for alpha-rays from Np with an energy of 4.78 MeV, 120 keV (= 2.2%) for those with 5.49 MeV from Am, and 109 keV (= 1.9%) for those with 5.81 MeV from Cm. It is found that the energy resolution obtained at the present experiment is dominated in the electronic noise caused by the large capacitance existed between the collecting anode (CA) and non-collecting anode (NCA) in the coplanar electrode. (author)

Pulser injection with subsequent removal for gamma-ray spectrometry

International Nuclear Information System (INIS)

Hartwell, J.K.; Goodwin, S.G.; Johnson, L.O.; Killian, E.W.

1990-01-01

This patent describes a module for use with a gamma-ray spectroscopy system. The system includes a gamma-ray detector for detecting gamma-ray events and producing a signal representing the gamma-ray events, a converter responsive to the detector and capable of converting the signal to a spectrum, a storage memory responsive to the converter and capable of storing the spectrum at address locations in memory, and a pulser capable of injecting pulses into the signal produced by the detector. The module comprises: means for generating a logic pulse for controlling the pulser, the controlling means adapted for coupling to the pulser; means for generating separation of events logic to isolate the components of a combined gamma-ray---pulse spectrum, the separation of events logic means adapted for coupling to the converter and the storage memory with the capability of storing pulses at address locations in the storage memory separate from the gamma-ray events; means for receiving an imitating signal from the converter to generate a plurality of operations by the module; means for tracking variations in a gamma-ray---pulse spectrum brought on by external parameter changes; and means for interfacing with commercially developed gamma-ray spectrometry equipment

Burn up determination of IEAR-1 fuel elements by non destructive gamma ray spectrometry method

International Nuclear Information System (INIS)

Soares, A.J.

1977-01-01

Measurement of nuclear fuel burn up by non destructive gamma ray spectrometry is discussed, and results of such measurements, made at the Instituto de Energia Atomica (IEA), are given. Specifically, the burn up of an MTR (Material Testing Reactor) fuel element removed from the IEAR-1 swimming pool reactor in 1958 is evaluated from the measured Cs-137 activity, which gives a single 661,6 keV gamma ray. Due to the long decay time of the test element, no other fission decay product activity could be detected. Analysis of measurements, made with a 3'' x 3'' NaI(Tl) detector at 330 distinct points of the element, showed the total burn up to 3.3 +- -+ 0.8 mg. This is in agreement with a calculated value. As the maximum temperature of IEAR-1 fuel elements is of the order of 40 0 C, migration effects of Cs-137 was not considered, this being significant only at fuel temperature in excess of 1000 0 C [pt

Simultaneous determination of actinides by x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Cohen, V.H.

1990-01-01

The x-ray spectrometric simultaneous determination of uranium and plutonium in simulated Purex Process solutions is described. The method is accomplished by intensity measurements of the L α sub(1) lines. The thin film technique for sample preparation and thorium as an internal standard had been used. An evaporation technique had been also tested for low concentration uranium solutions. In the measurement range 0,05 - 130 U g/L, 0,5 - 20 Pu g/L linear calibration curves were effected. The standard deviation in the concentration range 10 to 130 g/L was 3,5%, 4% in the 1 to 10 g/L and 13% in 0,05 to 1 g/L for uranium determination and 4% for plutonium determination in the range of 1 to 20 g/L. The sensitivity of the method was about 3,62 μg to U and 3,95 μg to Pu. Uranium and plutonium do not reciprocally interfere with one another until U/Pu ≅ 90 m/m. The fission product as interfering elements were also verified. Finally, uranium and plutonium were determined in simulated Purex Process solutions within the requested accuracy for control method. (author)

Trace rare earth analysis by neutron activation and γ-ray/x-ray spectrometry

International Nuclear Information System (INIS)

Laul, J.C.; Nielson, K.K.; Wogman, N.A.

1977-01-01

A rare earth group separation scheme followed by photon energy analysis using Ge(Li) and intrinsic Ge detectors enhances significantly the detection of individual rare earth elements (REE) at or below the ppb level. Based on the x-ray and selected γ-ray energies, Ge(Li) γ-ray counting is favorable for 140 La, 141 Ce, 142 Pr, 153 Sm, 171 Er, and 177 Lu, whereas intrinsic Ge γ-ray counting is favorable for 143 Ce, 147 Nd, 160 Tb, and 166 Ho, and intrinsic Ge x-ray counting is favorable for 152 Eu and 175 Yb. Gamma-ray counting of 153 Gd and 170 Tm is equally sensitive with Ge(Li) or intrinsic Ge detectors. Precise measurements of the REE were made in the USGS geological samples BCR-1, W-1, AGV-1, G2, GSP-1 and PCC-1, the IAEA Soil-5, and the NBS orchard leaf and bovine liver standards. Their chondritic normalized REE patterns behave as a smooth function of the REE ionic radii. Interestingly, the REE patterns observed in orchard leaf and other plants are identical to the REE pattern in bovine liver. This comparison leads us to suggest that the plant REE patterns are probably not further fractionated by animals such as bovine during their dietary plant uptake

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

International Nuclear Information System (INIS)

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

2010-01-01

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

Design and characterization for absolute x-ray spectrometry in the 100-10,000 eV region

International Nuclear Information System (INIS)

Henke, B.L.

1986-08-01

Reviewed here are the design and characterization procedures used in our program for developing absolute x-ray spectrometry in the 100 to 10,000 eV region. Described are the selection and experimental calibration of the x-ray filters, mirror momochromators, crystal/multilayer analyzers, and the photographic (time integrating) and photoelectric (time resolving) position-sensitive detectors. Analytical response functions have been derived that characterize the energy dependence of the mirror and crystal/multilayer reflectivities and of the photographic film and photocathode sensitivities. These response functions permit rapid, small-computer reduction of the experimental spectra to absolute spectra (measured in photons per stearadian from the source for radiative transitions at indicated photon energies). Our x-ray spectrographic systems are being applied to the diagnostics of pulsed, high temperature plasma sources in laser fusion and x-ray laser research. 15 refs., 27 figs

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

International Nuclear Information System (INIS)

Dian Anggraini; Rosika Kriswarini; Yusuf N

2007-01-01

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

Fast procedures for coincidence-summing correction in γ-ray spectrometry

International Nuclear Information System (INIS)

De Felice, Pierino; Angelini, Paola; Fazio, Aldo; Biagini, Roberto

2000-01-01

Simplified and fast procedures for coincidence-summing correction in γ-ray spectrometry were investigated. These procedures are based on the usual theoretical expressions of the correction factors, but differ in the determination of the total efficiency curve based on the following approximations: (a) replacement, below the knee efficiency value, of the total efficiency by the full-energy peak efficiency; and (b) use of linear interpolations (in log-log plot) between only two experimental points above the knee efficiency value; or (c) assumption of a peak-to-total efficiency ratio independent on the counting geometry; or (d) assumption of a constant relation between the peak-to-total efficiency ratios and the photoelectric-to-total cross section ratios. The above approximations were separately assumed for determination of the coincidence-summing correction factors for nuclides with complex decay scheme ( 133 Ba, 134 Cs, 152 Eu) and for 60 Co and 88 Y measured on a 15% relative efficiency p-type coaxial HPGe detector, for three source-detector geometries: point source placed on top of and at 10 cm from the detector window, and 1 l Marinelli beaker filled with aqueous solution. The results were compared with those based on more accurate experimental determinations of the total efficiency curve from measurements of standard sources of eight different single-γ-ray emitters. The usefulness of each simplified procedure is evaluated with respect to its accuracy and to the reduction of the number of standard sources and measurement time

Rapid analysis of 226Ra in mine waters by gamma-ray spectrometry. Supervising Scientist report 103

International Nuclear Information System (INIS)

Johnston, A.; Martin, P.

1995-01-01

Techniques for the determination of 226 Ra in uranium mine waters by γ-ray spectrometry are examined with an emphasis on methods capable of completion within 1 to 3 days of receipt of the sample. Methods discussed utilise either: (i) the 186 keV 226 Ra γ-ray, with the contribution from 235 U being subtracted after a separate uranium determination, or (ii) measurement of ingrowing 222 Rn progeny, either by two successive counts or by a single count (together with an assumption that radon was not present at the time of sample preparation). A full analysis of the statistical uncertainties and systematic errors associated with each technique is presented

Single particle transfer for quantitative analysis with total-reflection X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Esaka, Fumitaka; Esaka, Konomi T.; Magara, Masaaki; Sakurai, Satoshi; Usuda, Shigekazu; Watanabe, Kazuo

2006-01-01

The technique of single particle transfer was applied to quantitative analysis with total-reflection X-ray fluorescence (TXRF) spectrometry. The technique was evaluated by performing quantitative analysis of individual Cu particles with diameters between 3.9 and 13.2 μm. The direct quantitative analysis of the Cu particle transferred onto a Si carrier gave a discrepancy between measured and calculated Cu amounts due to the absorption effects of incident and fluorescent X-rays within the particle. By the correction for the absorption effects, the Cu amounts in individual particles could be determined with the deviation within 10.5%. When the Cu particles were dissolved with HNO 3 solution prior to the TXRF analysis, the deviation was improved to be within 3.8%. In this case, no correction for the absorption effects was needed for quantification

In situ measurements in an immerged environment of ambient gamma radiation activity and associated spectrometry

International Nuclear Information System (INIS)

Metivier, J.

1993-01-01

A set of site measurement devices composed of an ictometer, an air ionization chamber and a gamma ray spectrometry chain was modified so that the type of measurements could be carried out in an immerged environment with the equipment lying on the sediments of the prospected area. The different detectors can be controlled-and the data stored in a portable and autonomous 'PC' microcomputer from a light craft

Plutonium isotopic measurements by gamma-ray spectroscopy

International Nuclear Information System (INIS)

Haas, F.X.; Lemming, J.F.

1976-01-01

A nondestructive technique is described for calculating plutonium-238, plutonium-240, plutonium-241 and americium-241 relative to plutonium-239 from measured peak areas in the high resolution gamma-ray spectra of solid plutonium samples. Gamma-ray attenuation effects were minimized by selecting sets of neighboring peaks in the spectrum whose components are due to the different isotopes. Since the detector efficiencies are approximately the same for adjacent peaks, the accuracy of the isotopic ratios is dependent on the half-lives, branching intensities, and measured peak areas. The data presented describe the results obtained by analyzing gamma-ray spectra in the energy region from 120 to 700 keV. Most of the data analyzed were obtained from plutonium material containing 6 percent plutonium-240. Sample weights varied from 0.25 g to approximately 1.2 kg. The methods were also applied to plutonium samples containing up to 23 percent plutonium-240 with weights of 0.25 to 200 g. Results obtained by gamma-ray spectroscopy are compared to chemical analyses of aliquots taken from the bulk samples

Characterization of Roman glass tesserae from the Coriglia excavation site (Italy) via energy-dispersive X-ray fluorescence spectrometry and Raman spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Donais, Mary Kate; Sparks, Andrew; Redente, Monica [Saint Anselm College, Department of Chemistry, Manchester, NH (United States); Pevenage, Jolien van; Moens, Luc; Vincze, Laszlo [Ghent University, Department of Analytical Chemistry, Ghent (Belgium); George, David B. [Saint Anselm College, Department of Classics, Manchester, NH (United States); Vandenabeele, Peter [Ghent University, Department of Archaeology, Ghent (Belgium)

2016-12-15

The combined use of handheld energy-dispersive X-ray fluorescence spectrometry, Raman spectroscopy, and micro-energy-dispersive X-ray fluorescence spectrometry permitted the characterization of Roman glass tesserae excavation from the Coriglia (Italy) archeological site. Analyses of ten different glass colors were conducted as spot analyses on intact samples and as both spot analyses and line scans on select cross-sectioned samples. The elemental and molecular information gained from these spectral measurements allowed for the qualitative chemical characterization of the bulk glass, decolorants, opacifiers, and coloring agents. The use of an antimony opacifier in many of the samples supports the late Imperial phasing as determined through numismatic, fresco, ceramics, and architectural evidence. And dealinization of the exterior glass layers caused by the burial environment was confirmed. (orig.)

Time-resolved and position-resolved X-ray spectrometry with a pixelated detector

Energy Technology Data Exchange (ETDEWEB)

Sievers, Peter

2012-12-07

show a good agreement. Up to now the measurements of impinging spectra with a Timepix detector have been performed in radiation fields with a relatively high fluence. To cope with the requirement of measuring in radiation fields with a low fluence, there had to be changes in the method of analysis compared to those performed formerly. An important improvement in this context was the employment of the Bayesian deconvolution method. The spectra reconstructed with this method were then compared to the results of two different and established detection systems. Firstly, the shape of the deconvolved spectrum was compared to the one measured with a hpGe detector. Secondly, the calculated value of the kerma rate was compared to the one measured with an ionization chamber. This gave an estimate on the correctness of the absolute number of photons. Both comparisons have shown a good agreement and thus I was able to validate that the method delivers precise results. Compared to the formerly used spectrum-stripping method the Bayesian deconvolution turned out to be very stable and reliable. This robustness of the deconvolution method and the development of a pixel-by-pixel energy calibration were the keys towards position-resolved spectrometry. With such a precise energy calibration the energy resolution was enhanced by up to 45%. This improved accuracy in the measurement has been very demanding on the improvements of the simulation of the response matrix needed for deconvolution. Both this enhanced simulation and a pixel-by-pixel calibrated detector opened the possibility of measuring the anode heel effect. Not only the relative angular dependency of the spectrum emitted but also the change in the absolute photon fluence were measured. Furthermore, it is possible to even use small ROIs down to 4x4 pixels to evaluate a spectrum. This was then applied for the spectrometry of small focal spots of a miniature X-ray source used in therapeutics. Furthermore, the robustness and the

Time-resolved and position-resolved X-ray spectrometry with a pixelated detector

International Nuclear Information System (INIS)

Sievers, Peter

2012-01-01

show a good agreement. Up to now the measurements of impinging spectra with a Timepix detector have been performed in radiation fields with a relatively high fluence. To cope with the requirement of measuring in radiation fields with a low fluence, there had to be changes in the method of analysis compared to those performed formerly. An important improvement in this context was the employment of the Bayesian deconvolution method. The spectra reconstructed with this method were then compared to the results of two different and established detection systems. Firstly, the shape of the deconvolved spectrum was compared to the one measured with a hpGe detector. Secondly, the calculated value of the kerma rate was compared to the one measured with an ionization chamber. This gave an estimate on the correctness of the absolute number of photons. Both comparisons have shown a good agreement and thus I was able to validate that the method delivers precise results. Compared to the formerly used spectrum-stripping method the Bayesian deconvolution turned out to be very stable and reliable. This robustness of the deconvolution method and the development of a pixel-by-pixel energy calibration were the keys towards position-resolved spectrometry. With such a precise energy calibration the energy resolution was enhanced by up to 45%. This improved accuracy in the measurement has been very demanding on the improvements of the simulation of the response matrix needed for deconvolution. Both this enhanced simulation and a pixel-by-pixel calibrated detector opened the possibility of measuring the anode heel effect. Not only the relative angular dependency of the spectrum emitted but also the change in the absolute photon fluence were measured. Furthermore, it is possible to even use small ROIs down to 4x4 pixels to evaluate a spectrum. This was then applied for the spectrometry of small focal spots of a miniature X-ray source used in therapeutics. Furthermore, the robustness and the

Nondestructive and quantitative characterization of TRU and LLW mixed-waste using active and passive gamma-ray spectrometry and computed tomography

Energy Technology Data Exchange (ETDEWEB)

Camp, D.C.; Martz, H.E.

1991-11-12

The technology being proposed by LLNL is an Active and Passive Computed Tomography (A P CT) Drum Scanner for contact-handled (CH) wastes. It combines the advantages offered by two well-developed nondestructive assay technologies: gamma-ray spectrometry and computed tomography (CT). Coupled together, these two technologies offer to nondestructively and quantitatively characterize mixed- wastes forms. Gamma-ray spectroscopy uses one or more external radiation detectors to passively and nondestructively measure the energy spectrum emitted from a closed container. From the resulting spectrum one can identify most radioactivities detected, be they transuranic isotopes, mixed-fission products, activation products or environmental radioactivities. Spectral libraries exist at LLNL for all four. Active (A) or transmission CT is a well-developed, nondestructive medical and industrial technique that uses an external-radiation beam to map regions of varying attenuation within a container. Passive (P) or emission CT is a technique mainly developed for medical application, e.g., single-photon emission CT. Nondestructive industrial uses of PCT are under development and just coming into use. This report discuses work on the A P CT Drum Scanner at LLNL.

Porosity measurement of amorphous materials by gamma ray transmission

International Nuclear Information System (INIS)

Poettker, Walmir Eno

2000-01-01

In this work it is presented the measurement of the total porosity of TRe soil, Sandstone Berea rocks and porous ceramics samples. For the determination of the total porosity, the Arquimedes method (conventional) and the gamma ray transmission methodology were employed. The porosity measurement using the gamma methodology has a significant advantage respect to the conventional method due to the fast and non-destructive determination, and also for supplying results with a greater characterization in small scales, in relation to the heterogeneity of the porosity. The conventional methodology presents good results only for homogeneous samples. The experimental set up for the gamma ray transmission technique consisted of a 241 Am source (59,53 keV), a NaI (Tl) scintillation detector, collimators, a XYZ, micrometric table and standard gamma spectrometry electronics connected to a multichannel analyser. (author)

X-ray beam penetration in TXRF measurement of polycrystalline and amorphous surfaces

International Nuclear Information System (INIS)

Ghatak-Roy, A.R.; Hossain, T.Z.

2000-01-01

For TXRF measurement on single crystal silicon surface, it is generally agreed that the x-ray beam penetration is of the order of a few hundred Angstroms from the surface. However, for polycrystalline and amorphous surfaces - frequently used in semiconductor manufacturing there are evidences that x-rays penetrate much deeper revealing underlying layers. The evidences come from various measurements done with films such as silicon dioxide, silicon nitride and metal films such as aluminum, titanium and cobalt. A systematic study was carried out to help understand the issue further. Four sets of samples (on 8 inch wafers) were prepared to create layers buried under various deposited metal and non-metal layers. The metal layers created were aluminum, titanium and cobalt and the non-metal layers were silicon dioxide and silicon nitride. These samples were analyzed by TXRF under various angles and energies and the data were analyzed for signals from various buried layers along with their angular dependence. The results indicated deep penetration of x-ray beams. The samples were further analyzed by SIMS (Secondary Ion Mass Spectrometry) and some of them by ICP-MS (Inductively Coupled Plasma - Mass Spectrometry) to obtain information about their depth profiles. This was done in order to rule out the possibility of intermixing of layers during deposition. (author)

Airborne gamma-ray spectrometry

DEFF Research Database (Denmark)

Hovgaard, Jens

A new method - Noise Adjusted Singular Value Decomposition, NASVD - for processing gamma-ray spectra has been developed as part of a Ph.D. project. By using this technique one is able to decompose a large set of data - for example from airborne gamma-ray surveys - into a few spectral components....... By knowing the spectral components and their amplitudes in each of the measured spectra one is able to extract more information from the data than possible with the methods used otherwise....

Heavy metal determination by X-rays spectrometry in superficial sediments at Havana Bay

International Nuclear Information System (INIS)

Gelen, Alina; Izquierdo, Walter; Lopez, Neivy; Corrales, Yasser; Casanova, Amaya O.; Diaz, Oscar; Manso, Maria V.; D'Alessandro, Katia; Reyes, Enma; Toledo, Carlos; Beltran, Jesus; Perez, Marlen; Ramirez, Marta; Soto, Jesus

2007-01-01

Havana Bay is a typical bag-type located in the Western-North Coast of the Republic of Cuba. Since 1980 it has been the object of a study for sea bottom rehabilitation and improvement of quality of the waters, where the final objective will be the recovery of the coastal and marine ecosystem. Thirteen surface samples of the Havana Bay (Cuba) were collected and analysed by X-Rays spectrometry. Some majority elements (Si, Ca, K, Na, S, Cl, Al, Fe, Mg, C and O) were measured by scanning electron microscopy (SEM) coupled with microanalysis to perform geomorphologic analysis. Nine elements (Ca, Fe, Ti, Mn, Cu, Zn, Sr, Zr and Pb) have been measured using an Energy Dispersive X-Ray Fluorescence (EDXRF) with a Si(Li) detector. Multivariate statistical was used for the analysis. The concentration levels showed this bay as the most polluted in Cuba. The highest contents of Cu, Zn and Pb were obtained in Atares and Marimelena Cove; these elements are indicators of urban as well as industrial pollution. (author)

Heavy metal determination by X-rays spectrometry in superficial sediments at Havana Bay

Energy Technology Data Exchange (ETDEWEB)

Gelen, Alina; Izquierdo, Walter; Lopez, Neivy; Corrales, Yasser; Casanova, Amaya O.; Diaz, Oscar; Manso, Maria V.; D' Alessandro, Katia [Institute for Applied Sciences and Technology, Havana (Cuba)], E-mail: alina@instec.cu; Reyes, Enma; Toledo, Carlos [Central Laboratory Criminology, Havana (Cuba); Beltran, Jesus; Perez, Marlen; Ramirez, Marta [Engineering Centre for Environmental Management of Bays and Coasts, Havana (Cuba)], E-mail: beltran@cimab.transnet.cu; Soto, Jesus [Universidad de Cantabria, Santander (Spain)], E-mail: sotoj@unican.es

2007-07-01

Havana Bay is a typical bag-type located in the Western-North Coast of the Republic of Cuba. Since 1980 it has been the object of a study for sea bottom rehabilitation and improvement of quality of the waters, where the final objective will be the recovery of the coastal and marine ecosystem. Thirteen surface samples of the Havana Bay (Cuba) were collected and analysed by X-Rays spectrometry. Some majority elements (Si, Ca, K, Na, S, Cl, Al, Fe, Mg, C and O) were measured by scanning electron microscopy (SEM) coupled with microanalysis to perform geomorphologic analysis. Nine elements (Ca, Fe, Ti, Mn, Cu, Zn, Sr, Zr and Pb) have been measured using an Energy Dispersive X-Ray Fluorescence (EDXRF) with a Si(Li) detector. Multivariate statistical was used for the analysis. The concentration levels showed this bay as the most polluted in Cuba. The highest contents of Cu, Zn and Pb were obtained in Atares and Marimelena Cove; these elements are indicators of urban as well as industrial pollution. (author)

Spiked environmental matrix for use as a reference material for gamma-ray spectrometry: Production and homogeneity test

International Nuclear Information System (INIS)

Sobiech-Matura, K.; Máté, B.; Altzitzoglou, T.

2016-01-01

The application of a spiking method for reference material production and its utilisation for a food matrix is presented. The raw rice powder was tested by means of γ-ray spectrometry and spiked with a "1"3"7Cs solution. The spiked material was mixed and tested for homogeneity. The future use of the rice powder reference material after the entire characterisation cycle will be for γ-ray spectrometry method validation. - Highlights: • Spiking blank substance with a traceable radioactive solution • Spiked reference material for γ-ray emitting radionuclides in food matrix • Results of the homogeneity tests are presented

Development of multilayer optics for X-ray broadband spectrometry of plasma emission

International Nuclear Information System (INIS)

Emprin, Benoit

2014-01-01

Within the framework of the research on inertial confinement fusion, the 'Commissariat a l'energie atomique et aux energies alternatives' has studied and implemented an absolute calibrated time-Resolved broadband soft x-Ray spectrometer, called 'Diagnostic de Mesure du rayonnement X'. This diagnostic, composed of 20 measurement channels, measures the emitted radiant power from a laser created plasma in the range from 50 eV to 20 keV. We have developed additional measurement channels to obtain redundancy and an improvement in measurement accuracy. The principle of these new channels is based on an original concept to obtain spectral bounded flat-Responses. Two channels have been developed for the 2 - 4 keV and 4 - 6 keV spectral ranges, using aperiodic multilayer mirrors made at the 'Laboratoire Charles Fabry' with Cr/Sc and Ni/W/SiC/W layers respectively. These mirrors were characterized at synchrotron radiation facilities and integrated into the spectrometer. The two new channels were used during laser-Plasma experimental campaigns at the OMEGA laser facility in Rochester (USA). This allowed us to determine directly the radiant power with only one measurement within a certain spectral band, and with a better precision when compared with using standard channels. The results, in good agreement with the standard measurement channels, allowed us to validate the use of aperiodic multilayer mirrors for X-Ray broadband spectrometry. (author) [fr

Evaluation of TASTEX task H: measurement of plutonium isotopic abundances by gamma-ray spectrometry

International Nuclear Information System (INIS)

Gunnink, R.; Prindle, A.L.; Asakura, Y.; Masui, J.; Ishiguro, N.; Kawasaki, A.; Kataoka, S.

1981-10-01

This report describes a computer-based gamma spectrometer system that was developed for measuring isotopic and total plutonium concentrations in nitric acid solutions. The system was installed at the Tokai reprocessing plant where it is undergoing testing and evaluation as part of the Tokai Advanced Safeguards Exercise (TASTEX). Objectives of TASTEX Task H, High-Resolution Gamma Spectrometer for Plutonium Isotopic Analysis, the methods and equipment used, the installation and calibration of the system, and the measurements obtained from several reprocessing campaigns are discussed and described. In general, we find that measurements for gamma spectroscopy agree well with those of mass spectrometry and of other chemical analysis. The system measures both freshly processed plutonium from the product accountability tank and aged plutonium solutions from storage tanks. 14 figures, 15 tables

Proceedings of the International Symposium Advances in alpha, Beta- and Gamma-Ray spectrometry

International Nuclear Information System (INIS)

1997-01-01

The International Committee for Radionuclide Metrology (ICRM) is an association of radionuclide metrology laboratories whose membership is composed of delegates of these laboratories together with other scientists actively engaged in the study and applications of radioactivity. The scientific activities are carried out in the frame of six Working Groups. Two of them, the Alpha-Particle Spectrometry and the Gamma-and Beta-ray Spectrometry Working Groups held a common workshop in Pushkin, St. Petersburg, 18 to 20 September 1996, under the title Advances in Alpha-Beta-and Gamma-Ray Sepectrometry, at the kind invitation of the D.I. Mendeleyev Institute for Metrology. More than 30 people from 14 laboratories attended the meeting, and nineteen oral communications were presented, from which twelve were retained for publication an are included in these proceedings. (Author)

Determination of C and O and other elements by alpha-induced X-ray energy spectrometry

International Nuclear Information System (INIS)

Henningsen, W.P.; Schaetzler, H.P.; Kuehn, W.

1978-01-01

X-ray energy spectrometry combined with alpha-excitation by means of radionuclides, especially Po-210, has been found as a versatile tool for multielement analysis. Down to Z = 6 (carbon) qualitative and quantitative measurements have been carried out with energy resolution good enough to separate adjacent elements. Thereby errors and lowest detectable concentrations were in the region of one percent. By utilizing M- and L-X-radiation the set of detectable elements can be opened to high atomic numbers. As an example with special regard to environmental research cadmium in organic matrix was measured down to 100 ppm without any preconcentration. Much lower detection limits might be reached by appropriate measures. (orig.) [de

Measurement of planetary surface composition by gamma-ray and neutron spectrometry - Preparatory studies for Mars and for the Moon by numerical simulations

International Nuclear Information System (INIS)

Gasnault, O.

1999-01-01

Gamma-ray and neutron spectrometry sets up a powerful tool of geological and geochemical characterization of planetary surfaces. This method allows to tackle some critical planet science questions: crustal and mantle compositions; ices; volcanism; alteration processes... Most of the neutrons and gamma photons result from the interactions of galactic cosmic rays with matter. The first chapter introduces the physics of these nuclear interactions in planetary soils and in detectors. Our work aims at optimizing the observations by specifying instrumental performances, and by highlighting relations between soil composition and neutron fluxes. Numerical simulations using the GEANT code from CERN support our analysis. The second chapter estimates the performances of the Germanium gamma-ray spectrometer for MARS SURVEYOR 2001. The result of simulations is compared to calibration measurements; then performances are calculated in flight configuration. The background at Mars is estimated to about 160 c/s. The instrument offers a fine sensitivity to: Fe, Mg, K, Si, Th, Cl and O. It will also be possible to measure U, Ti, H, C, S, Ca and Al. The emission lobes at the surface are calculated too. These measurements shall permit a better understanding of the Martian surface. The last chapter deals with fast neutrons [500 keV; 10 MeV] emitted by the Moon. The strong influence of oxygen is underlined. As observed by LUNAR PROSPECTOR, the integrated flux shows a pronounced dependence with regolith content in iron and titanium, allowing the mapping. The influence of the other chemical elements is quantified. A simple mathematical formula is suggested to estimate the integrated neutron flux according to soil composition. At last, a study of hydrogen effects on fast neutron flux is carried out; we examine the possibilities to quantify its abundance in the soil by this method. (author)

An intercomparison of Monte Carlo codes used for in-situ gamma-ray spectrometry

International Nuclear Information System (INIS)

Hurtado, S.; Villa, M.

2010-01-01

In-situ gamma-ray spectrometry is widely used for monitoring of natural as well as man-made radionuclides and corresponding gamma fields in the environment or working places. It finds effective application in the operational and accidental monitoring of nuclear facilities and their vicinity, waste depositories, radioactive contamination measurements and environmental mapping or geological prospecting. In order to determine accurate radionuclide concentrations in these research fields, Monte Carlo codes have recently been used to obtain the efficiency calibration of in-situ gamma-ray detectors. This work presents an inter-comparison between two Monte Carlo codes applied to in-situ gamma-ray spectrometry. On the commercial market, Canberra has its LABSOCS/ISOCS software which is relatively inexpensive. The ISOCS mathematical efficiency calibration software uses a combination of Monte Carlo calculations and discrete ordinate attenuation computations. Efficiencies can be generated in a few minutes in the field and can be modified easily if needed. However, it has been reported in the literature that ISOCS computation method is accurate on average only within 5%, and additionally in order to use LABSOCS/ISOCS it is necessary a previous characterization of the detector by Canberra, which is an expensive process. On the other hand, the multipurpose and open source GEANT4 takes significant computer time and presents a non-friendly but powerful toolkit, independent of the manufacturer of the detector. Different experimental measurements of calibrated sources were performed with a Canberra portable HPGe detector and compared to the results obtained using both Monte Carlo codes. Furthermore, a variety of efficiency calibrations for different radioactive source distributions were calculated and tested, like plane shapes or containers filled with different materials such as soil, water, etc. LabSOCS simulated efficiencies for medium and high energies were given within an

Self-absorption corrections of various sample-detector geometries in gamma-ray spectrometry using sample Monte Carlo Simulations

International Nuclear Information System (INIS)

Ahmad Saat; Appleby, P.G.; Nolan, P.J.

1997-01-01

Corrections for self-absorption in gamma-ray spectrometry have been developed using a simple Monte Carlo simulation technique. The simulation enables the calculation of gamma-ray path lengths in the sample which, using available data, can be used to calculate self-absorption correction factors. The simulation was carried out on three sample geometries: disk, Marinelli beaker, and cylinder (for well-type detectors). Mathematical models and experimental measurements are used to evaluate the simulations. A good agreement of within a few percents was observed. The simulation results are also in good agreement with those reported in the literature. The simulation code was carried out in FORTRAN 90,

Chemical analysis of zinc electroplating solutions by x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Jung, Sung-Mo; Cho, Young-Mo; Na, Han-Gil

2007-01-01

A quantitative analysis method used to analyze chlorine, iron and zinc in electroplating solutions, using X-ray spectrometry in atmospheric He mode, is proposed. The present research concerns the replacement of the conventional analyses of electroplating solutions with rapid and reproducible quantification using X-ray fluorescence spectrometer. An in-depth investigation conducted in the present study identifies the species present in the real electroplating solutions. XRD patterns and semi-quantitative results for the electroplating solutions show synthetic standards based on the compositional range of solutions by analyzing the electroplating solutions obtained in real processes. 28 calibration standard solutions are prepared by diluting liquid standard solutions certified by titration and ICP-OES analyses used to construct the XRF calibration curves for Cl, Fe and Zn. The suggested method showed satisfactory precision and accuracy in the analysis of electroplating solutions. The present study provides evidences that the proposed XRF spectrometry could be an alternative analytical method to replace the conventional techniques by comparing the uncertainties estimated for each method. (author)

Self-attenuation correction in the environmental sample gamma spectrometry; Correcao de auto-absorcao na espectrometria gama de amostras ambientais

Energy Technology Data Exchange (ETDEWEB)

Venturini, Luzia; Nisti, Marcelo B. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)

1997-10-01

Self-attenuation corrections were calculated for gamma ray spectrometry of environmental samples with densities from 0.42 g/ml up to 1.59 g/ml, measured in Marinelli beakers and polyethylene flasks. These corrections are to be used when the counting efficiency is calculated for water measured in the same geometry. The model of Debertin for Marinelli beaker, numerical integration and experimental linear attenuation coefficients were used. (author). 3 refs., 4 figs., 6 tabs.

Use of airborne gamma-ray spectrometry for kaolin exploration

Science.gov (United States)

Tourlière, B.; Perrin, J.; Le Berre, P.; Pasquet, J. F.

2003-08-01

Airborne gamma-ray spectrometry was used to define targets with kaolin potential in the Armorican Massif of Brittany, France. This exploration method is based on the principle that kaolinite, an aluminosilicate clay mineral constituting kaolin, is formed by the hydrolysis of potash feldspar with the elimination of potassium. Therefore, potassium contrast between favourable host-rock such as a leucogranite and kaolin occurrence is likely a significant pathfinder. As the relationship between the potassium-40 recorded by an airborne gamma-ray spectrometer and total potassium is constant, such data provide us a direct measurement of the potassium content of the ground flown over. Our study tested this by calculating, for each geological unit, the difference between the measured and average potassium content calculated for a given geological formation. The study was based on (i) a recent (1998) high-definition airborne geophysical survey over the Armorican Massif undertaken on behalf of the French Government, and (ii) new geological compilation maps covering the same region. Depleted zones, where the measured potassium is less than the average potassium content calculated target areas with high potential of containing kaolin, provided that the unit was originally rich in potash feldspar. By applying this method to the entire Armorican Massif, it was possible to identify 150 potassium-depleted zones, including 115 that were subjected to rapid field checks and 36 that contained kaolin (21 new discoveries). This method, which is both safe for the environment and easy to use, is therefore a good tool for rapidly defining targets with kaolin potential at a regional scale. The method may also have possibilities in exploring for other types of deposit characterised by an enrichment or depletion in U, K and/or Th.

Feasibility study of plutonium isotopic analysis of resin beads by nondestructive gamma-ray spectroscopy

International Nuclear Information System (INIS)

Li, T.K.

1985-01-01

We have initiated a feasibility study on the use of nondestructive low-energy gamma-ray spectroscopy for plutonium isotopic analysis on resin beads. Seven resin bead samples were measured, with each sample containing an average of 9 μg of plutonium; the isotopic compositions of the samples varied over a wide range. The gamma-ray spectroscopy results, obtained from 4-h counting-time measurements, were compared with mass spectrometry results. The average ratios of gamma-ray spectroscopy to mass spectrometry were 1.014 +- 0.025 for 238 Pu/ 239 Pu, 0.996 +- 0.018 for 240 Pu/ 239 Pu, and 0.980 +- 0.038 for 241 Pu/ 239 Pu. The rapid, automated, and accurate nondestructive isotopic analysis of resin beads may be very useful to process technicians and International Atomic Energy Agency inspectors. 3 refs., 1 fig., 3 tabs

Gamma-ray spectrometry of granitic suites of the Paranaguá Terrane, Southern Brazil

Science.gov (United States)

Weihermann, Jessica Derkacz; Ferreira, Francisco José Fonseca; Cury, Leonardo Fadel; da Silveira, Claudinei Taborda

2016-09-01

The Paranaguá Terrane, located in the coastal portion of the states of Santa Catarina, Paraná and São Paulo in Southern Brazil is a crustal segment constituted mainly by an igneous complex, with a variety of granitic rocks inserted into the Serra do Mar ridge. The average altitude is approximately 1200 m above sea level, with peaks of up to 1800 m. Due to the difficulty of accessing the area, a shortage of outcrops and the thick weathering mantle, this terrane is understudied. This research aims to evaluate the gamma-ray spectrometry data of the granitic suites of the Paranaguá Terrane, in correspondence with the geological, petrographical, lithogeochemical, relief and mass movement information available in the literature. Aerogeophysical data were acquired along north-south lines spaced at 500 m, with a mean terrain clearance of 100 m. These data cover potassium (K, %), equivalent in thorium (eTh, ppm) and equivalent in uranium (eU, ppm). After performing a critical analysis of the data, basic (K, eU, eTh) and ternary (R-K/G-eTh/B-eU) maps were generated and then superimposed on the digital elevation model (DEM). The investigation of the radionuclide mobility across the relief and weathering mantle consisted of an analysis of the schematic profiles of elevation related with each radionuclide; a comparison of the K, eU and eTh maps with their 3D correspondents; and the study of mass movements registered in the region. A statistical comparison of lithogeochemical (K, U, Th) and geophysical (K, eU, eTh) data showed consistency in all the granitic suites studied (Morro Inglês, Rio do Poço and Canavieiras-Estrela). Through gamma-ray spectrometry, it was possible to establish relationships between scars (from mass movements) and the gamma-ray responses as well as the radionuclide mobility and the relief and to map the granitic bodies.

Multi-spectra Cosmic Ray Flux Measurement

Science.gov (United States)

He, Xiaochun; Dayananda, Mathes

2010-02-01

The Earth's upper atmosphere is constantly bombarded by rain of charged particles known as primary cosmic rays. These primary cosmic rays will collide with the atmospheric molecules and create extensive secondary particles which shower downward to the surface of the Earth. In recent years, a few studies have been done regarding to the applications of the cosmic ray measurements and the correlations between the Earth's climate conditions and the cosmic ray fluxes [1,2,3]. Most of the particles, which reach to the surface of the Earth, are muons together with a small percentage of electrons, gammas, neutrons, etc. At Georgia State University, multiple cosmic ray particle detectors have been constructed to measure the fluxes and energy distributions of the secondary cosmic ray particles. In this presentation, we will briefly describe these prototype detectors and show the preliminary test results. Reference: [1] K.Borozdin, G.Hogan, C.Morris, W.Priedhorsky, A.Saunders, L.Shultz, M.Teasdale, Nature, Vol.422, 277 (2003). [2] L.V. Egorova, V. Ya Vovk, O.A. Troshichev, Journal of Atmospheric and Terrestrial Physics 62, 955-966 (2000). [3] Henrik Svensmark, Phy. Rev. Lett. 81, 5027 (1998). )

Detection limits should be a thing of the past in gamma-ray spectrometry in general as well as in neutron activation analysis

NARCIS (Netherlands)

Blaauw, Menno

2016-01-01

In gamma-ray spectrometry with high-resolution detectors, full-energy peaks are often to be detected by a peak-search algorithm, with a threshold for detection. Detection limits can be derived from this. Detection limits are often computed along with measured activities or concentrations. When an

Cosmic-ray neutron simulations and measurements in Taiwan

International Nuclear Information System (INIS)

Chen, Wei-Lin; Jiang, Shiang-Huei; Sheu, Rong-Jiun

2014-01-01

This study used simulations of galactic cosmic ray in the atmosphere to investigate the neutron background environment in Taiwan, emphasising its altitude dependence and spectrum variation near interfaces. The calculated results were analysed and compared with two measurements. The first measurement was a mobile neutron survey from sea level up to 3275 m in altitude conducted using a car-mounted high-sensitivity neutron detector. The second was a previous measured result focusing on the changes in neutron spectra near air/ground and air/water interfaces. The attenuation length of cosmic-ray neutrons in the lower atmosphere was estimated to be 163 g cm -2 in Taiwan. Cosmic-ray neutron spectra vary with altitude and especially near interfaces. The determined spectra near the air/ground and air/water interfaces agree well with measurements for neutrons below 10 MeV. However, the high-energy portion of spectra was observed to be much higher than our previous estimation. Because high-energy neutrons contribute substantially to a dose evaluation, revising the annual sea-level effective dose from cosmic-ray neutrons at ground level in Taiwan to 35 μSv, which corresponds to a neutron flux of 5.30 x 10 -3 n cm -2 s -1 , was suggested. The cosmic-ray neutron background in Taiwan was studied using the FLUKA simulations and field measurements. A new measurement was performed using a car-mounted high-efficiency neutron detector, re-coding real-time neutron counting rates from sea level up to 3275 m. The attenuation of cosmic-ray neutrons in the lower atmosphere exhibited an effective attenuation length of 163 g cm -2 . The calculated neutron counting rates over predicted the measurements by ∼32 %, which leaded to a correction factor for the FLUKA-calculated cosmic-ray neutrons in the lower atmosphere in Taiwan. In addition, a previous measurement regarding neutron spectrum variation near the air/ground and air/water interfaces was re-evaluated. The results showed that the

LabVIEW interface with Tango control system for a multi-technique X-ray spectrometry IAEA beamline end-station at Elettra Sincrotrone Trieste

Energy Technology Data Exchange (ETDEWEB)

Wrobel, P.M. [Physics Section, Nuclear Science and Instrumentation Laboratory (NSIL), IAEA Laboratories, A-2444 Seibersdorf (Austria); AGH University of Science and Technology, Faculty of Physics and Applied Computer Science, al. A. Mickiewicza 30, 30-059 Krakow (Poland); Bogovac, M. [Physics Section, Nuclear Science and Instrumentation Laboratory (NSIL), IAEA Laboratories, A-2444 Seibersdorf (Austria); Sghaier, H. [Physics Section, Nuclear Science and Instrumentation Laboratory (NSIL), IAEA Laboratories, A-2444 Seibersdorf (Austria); Institut Superieur d’Informatique et de Mathematiques de Monastir (ISIMM), Departement de technologie, 5000 Monastir (Tunisia); Leani, J.J. [Physics Section, Nuclear Science and Instrumentation Laboratory (NSIL), IAEA Laboratories, A-2444 Seibersdorf (Austria); IFEG – CONICET, Facultad de Matematica Astronomia y Fisica, Universidad Nacional de Cordoba, 5000 Cordoba (Argentina); Migliori, A.; Padilla-Alvarez, R. [Physics Section, Nuclear Science and Instrumentation Laboratory (NSIL), IAEA Laboratories, A-2444 Seibersdorf (Austria); Czyzycki, M. [Physics Section, Nuclear Science and Instrumentation Laboratory (NSIL), IAEA Laboratories, A-2444 Seibersdorf (Austria); AGH University of Science and Technology, Faculty of Physics and Applied Computer Science, al. A. Mickiewicza 30, 30-059 Krakow (Poland); Osan, J. [Physics Section, Nuclear Science and Instrumentation Laboratory (NSIL), IAEA Laboratories, A-2444 Seibersdorf (Austria); Environmental Physics Department, Hungarian Academy of Sciences Centre for Energy Research, Konkoly-Thege M. út 29-33., H-1121 Budapest (Hungary); Kaiser, R.B. [Physics Section, Nuclear Science and Instrumentation Laboratory (NSIL), IAEA Laboratories, A-2444 Seibersdorf (Austria); and others

2016-10-11

A new synchrotron beamline end-station for multipurpose X-ray spectrometry applications has been recently commissioned and it is currently accessible by end-users at the XRF beamline of Elettra Sincrotrone Trieste. The end-station consists of an ultra-high vacuum chamber that includes as main instrument a seven-axis motorized manipulator for sample and detectors positioning, different kinds of X-ray detectors and optical cameras. The beamline end-station allows performing measurements in different X-ray spectrometry techniques such as Microscopic X-Ray Fluorescence analysis (µXRF), Total Reflection X-Ray Fluorescence analysis (TXRF), Grazing Incidence/Exit X-Ray Fluorescence analysis (GI-XRF/GE-XRF), X-Ray Reflectometry (XRR), and X-Ray Absorption Spectroscopy (XAS). A LabVIEW Graphical User Interface (GUI) bound with Tango control system consisted of many custom made software modules is utilized as a user-friendly tool for control of the entire end-station hardware components. The present work describes this advanced Tango and LabVIEW software platform that utilizes in an optimal synergistic manner the merits and functionality of these well-established programming and equipment control tools. - Highlights: • A new methodology for control of a synchrotron beamline end-station is shown. • The new control system comprises a novel binding of Tango control system with LabVIEW interface. • The reliability of the control system is demonstrated by examples of analytical applications.

Determination of U, Th and K in bricks by gamma-ray spectrometry, X-ray fluorescence analysis and neutron activation analysis

Science.gov (United States)

Bártová, H.; Kučera, J.; Musílek, L.; Trojek, T.; Gregorová, E.

2017-11-01

Knowledge of the content of natural radionuclides in bricks can be important in some cases in dosimetry and application of ionizing radiation. Dosimetry of naturally occurring radionuclides in matter (NORM) in general is one of them, the other one, related to radiation protection, is radon exposure evaluation, and finally, it is needed for the thermoluminescence (TL) dating method. The internal dose rate inside bricks is caused mostly by contributions of the natural radionuclides 238U, 232Th, radionuclides of their decay chains, and 40K. The decay chain of 235U is usually much less important. The concentrations of 238U, 232Th and 40K were measured by various methods, namely by gamma-ray spectrometry, X-ray fluorescence analysis (XRF), and neutron activation analysis (NAA) which was used as a reference method. These methods were compared from the point of view of accuracy, limit of detection (LOD), amount of sample needed and sample handling, time demands, and instrument availability.

A low-energy set-up for gamma-ray spectrometry of NORM tailored to the needs of a secondary smelting facility.

Science.gov (United States)

Lutter, G; Schreurs, I Vandael; Croymans, T; Schroeyers, W; Schreurs, S; Hult, M; Marissens, G; Stroh, H; Tzika, F

2017-08-01

A measurement station dedicated for quantitative radiological characterisation of naturally occurring radionuclides in a metallurgical company and based on gamma-ray spectrometry was developed. The station is intended for performing quality control of final non-ferrous metal products and for radiological checks of incoming materials. A low-background point-contact HPGe-detector was used and the signal was split in two branches to enable collecting simultaneously spectra with high amplification (for gamma-ray energies below 250keV) and low amplification. Copyright © 2017 The Authors. Published by Elsevier Ltd.. All rights reserved.

Determination of zinc in ammoniacal ore leaching solutions by X-ray fluorescence spectrometry using a radioactive source

International Nuclear Information System (INIS)

Cornejo, N.; Afailal, A.; Garcia, F.; Palacios, M.

1994-01-01

A method was developed for the fast determination of zinc in leaching solutions by radioisotope energy-dispersive X-ray fluorescence (EDXRF) spectrometry. The measured intensities were used to develop regression models for estimating the zinc concentration. The primary radiation was provided by the 244 Cm radioisotope. Several experimental parameters including the saturation thickness and detection limit were determined. The advantages of the utilization of conditioning agents with elements of low atomic number such as nitric acid were established. (orig.)

Classification of soil samples according to their geographic origin using gamma-ray spectrometry and principal component analysis

International Nuclear Information System (INIS)

Dragovic, Snezana; Onjia, Antonije

2006-01-01

A principal component analysis (PCA) was used for classification of soil samples from different locations in Serbia and Montenegro. Based on activities of radionuclides ( 226 Ra, 238 U, 235 U, 4 K, 134 Cs, 137 Cs, 232 Th and 7 Be) detected by gamma-ray spectrometry, the classification of soils according to their geographical origin was performed. Application of PCA to our experimental data resulted in satisfactory classification rate (86.0% correctly classified samples). The obtained results indicate that gamma-ray spectrometry in conjunction with PCA is a viable tool for soil classification

X-ray fluorescence imaging with polycapillary X-ray optics

International Nuclear Information System (INIS)

Yonehara, Tasuku; Yamaguchi, Makoto; Tsuji, Kouichi

2010-01-01

X-ray fluorescence spectrometry imaging is a powerful tool to provide information about the chemical composition and elemental distribution of a specimen. X-ray fluorescence spectrometry images were conventionally obtained by using a μ-X-ray fluorescence spectrometry spectrometer, which requires scanning a sample. Faster X-ray fluorescence spectrometry imaging would be achieved by eliminating the process of sample scanning. Thus, we developed an X-ray fluorescence spectrometry imaging instrument without sample scanning by using polycapillary X-ray optics, which had energy filter characteristics caused by the energy dependence of the total reflection phenomenon. In the present paper, we show that two independent straight polycapillary X-ray optics could be used as an energy filter of X-rays for X-ray fluorescence. Only low energy X-rays were detected when the angle between the two optical axes was increased slightly. Energy-selective X-ray fluorescence spectrometry images with projection mode were taken by using an X-ray CCD camera equipped with two polycapillary optics. It was shown that Fe Kα (6.40 keV) and Cu Kα (8.04 keV) could be discriminated for Fe and Cu foils.

Nondestructive and quantitative characterization of TRU and LLW mixed-waste using active and passive gamma-ray spectrometry and computed tomography

International Nuclear Information System (INIS)

Camp, D.C.; Martz, H.E.

1991-01-01

The technology being proposed by LLNL is an Active and Passive Computed Tomography (A ampersand P CT) Drum Scanner for contact-handled (CH) wastes. It combines the advantages offered by two well-developed nondestructive assay technologies: gamma-ray spectrometry and computed tomography (CT). Coupled together, these two technologies offer to nondestructively and quantitatively characterize mixed- wastes forms. Gamma-ray spectroscopy uses one or more external radiation detectors to passively and nondestructively measure the energy spectrum emitted from a closed container. From the resulting spectrum one can identify most radioactivities detected, be they transuranic isotopes, mixed-fission products, activation products or environmental radioactivities. Spectral libraries exist at LLNL for all four. Active (A) or transmission CT is a well-developed, nondestructive medical and industrial technique that uses an external-radiation beam to map regions of varying attenuation within a container. Passive (P) or emission CT is a technique mainly developed for medical application, e.g., single-photon emission CT. Nondestructive industrial uses of PCT are under development and just coming into use. This report discuses work on the A ampersand P CT Drum Scanner at LLNL

Case Studies on Facility Characterization with X-Ray Fluorescence Spectrometry

International Nuclear Information System (INIS)

Kirk, K.T.; Brooksbank, R.D.; Meszaros, J.M.; Towery, W.E.

2008-01-01

A hand-held x-ray fluorescence (XRF) analyzer is being used to characterize facilities in support of demolition activities at the East Tennessee Technology Park (ETTP) in Oak Ridge, Tennessee. Approximately 500 facilities at the U.S. Department of Energy site are being demolished under the ETTP Decontamination and Decommissioning (D and D) project. Facility characterization is being conducted to provide data for waste profiling and identify hazards to demolition workers. XRF spectrometry is a non-destructive analytical technique used to identify and quantify the elemental composition of a substance based on the intensity of its characteristic X-ray emission wavelength or energy. The Innov-X Systems R Model XT-245S XRF analyzer used at ETTP is equipped with a silver anode x-ray tube and a Si PIN diode detector. X-rays are generated by electrical current, eliminating the need for radioactive isotopes. Electronic components can be powered by either a lithium-ion battery or an A/C adapter, and the instrument is controlled by an iPAQ R pocket personal computer. The unit has two primary operating modes. Alloy analysis mode measures percent levels of elements in metals such as a pipes, valves, equipment, or construction materials. Soil mode provides parts-per-million (ppm) quantities in bulk solids like concrete dust, residue, paint chips, or soil. The hand-held unit can analyze material in place, or it can analyze samples in a test stand by remote operation. This paper present some case studies demonstrating a variety of XRF applications for facility characterization: Metal Materials Characterization, Lead Paint Identification, Hot Spot Delineation, Bulk Solids Testing. XRF has been the analytical technique of choice for identifying metal alloy components and has also been useful in analyzing bulk materials. Limitations of XRF testing include the inability to directly analyze elements with low atomic weights. Light elements such as beryllium and aluminum do not emit

Spectral-ratio radon background correction method in airborne γ-ray spectrometry based on compton scattering deduction

International Nuclear Information System (INIS)

Gu Yi; Xiong Shengqing; Zhou Jianxin; Fan Zhengguo; Ge Liangquan

2014-01-01

γ-ray released by the radon daughter has severe impact on airborne γ-ray spectrometry. The spectral-ratio method is one of the best mathematical methods for radon background deduction in airborne γ-ray spectrometry. In this paper, an advanced spectral-ratio method was proposed which deducts Compton scattering ray by the fast Fourier transform rather than tripping ratios, the relationship between survey height and correction coefficient of the advanced spectral-ratio radon background correction method was studied, the advanced spectral-ratio radon background correction mathematic model was established, and the ground saturation model calibrating technology for correction coefficient was proposed. As for the advanced spectral-ratio radon background correction method, its applicability and correction efficiency are improved, and the application cost is saved. Furthermore, it can prevent the physical meaning lost and avoid the possible errors caused by matrix computation and mathematical fitting based on spectrum shape which is applied in traditional correction coefficient. (authors)

Plutonium isotopic measurements by gamma-ray spectroscopy

International Nuclear Information System (INIS)

Gunnink, R.

1973-11-01

A method is reported for analysis of isotopic and total plutonium by detecting and analyzing gamma rays emitted by the sample. A computerized prototype-system was developed and is now being routinely used at the Savannah River Plant for the nondestructive assay of solution samples. The analyses for 238 Pu, 239 Pu, 240 Pu, 241 Pu, and for 241 Am, when it is present, can be made in counting times as short as 10 to 15 minutes under optimum conditions. Comparison of isotopic ratio values with mass spectrometry generally shows agreement within 0.1 percent for 239 Pu and about 1 percent for 240 Pu and 241 Pu. Some preliminary isotopic measurements on solids are also discussed. (U.S.)

Development of Wavelet Based Tools for Improving the γ-ray Spectrometry

International Nuclear Information System (INIS)

Hamzaoui, E-M.; El Badri, L.; Laraki, K.; Cherkaoui-Elmorsli, R.

2013-06-01

In this article, we propose a wavelet transform based tool to improve the use of gamma ray spectrometry as a nuclear technique. First, we attempt to study the problem of filtering the preamplifier's output signals of HPGe detector used in the measurements chain. Thus, we developed a nonlinear method based on discrete Coiflet transform combined to principal component analysis, which allows a significant improvement of the signal to noise ratio (SNR) at the output of the HPGe preamplifier. In a second step, the continuous wavelet transform, based on the Mexican Hat mother function, is used to achieve an automatic processing of the spectrometric data. This method permits us to get an alternative representation of the gamma energy spectrum. The results of different tests, performed in both the presence and the absence of a gamma radiation source, are illustrated. (authors)

Distribution of heavy metals in Lumbricus terrestris, Aporrectodea longa and A. rosea measured by atomic absorption and X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Andersen, C.; Laursen, J.

1982-01-01

Distribution of Ca, Pb, Cd, Zn, Fe and Mn has been investigated in the earthworm species Lumbricus terrestris, Aporectodea longa and A. rosea by atomic absorption and X-ray fluorescence spectrometry measurements. The material of L. terrestris originated from the garden of the Royal Veterinary and Agricultural University in central Copenhagen. Material of the other two species was sampled in sewage sludge treated plots. It was found that lead and cadmium are accumulated in the gut wall and from here transferred to waste nodules (brown bodies). In L. terrestris more lead was transferred to waste nodules than cadmium. Also large amounts of zinc were accumulated in the gut wall. Analyses of L. terrestris calciferous glands showed that these take part in regulation and excretion of a number of heavy metals. Lead and cadmium content was low in the ventral nerve chord and seminal vesicles. A. longa with poorly developed calciferous glands seems to rely more on waste nodule formation in the ultimate immobilization of lead. (author)

Neutron activation analysis of lipsticks using gamma-ray spectrometry

International Nuclear Information System (INIS)

Mirsa, G.; Mittal, V.K.

2004-01-01

Neutron activation analysis with gamma-ray spectrometry was used to measure the concentrations of various elements in lipsticks of popular Indian and foreign brands. The aim of the present work was to study the possibility of existence of trace elements in samples of lipsticks (the ingredients of which are mostly organic in nature) and to see whether trace elements could distinguish lipsticks of different Indian and foreign brands from the forensic point of view apart from their inter-se differentiation. In the different samples of lipsticks that were analysed the following elements were detected: Au, Ba, Br, Ca, Cs, Fe, Na, Ru, Sb, Sc, Ta, Yb, Zn, Rb and Se. It was found that inter-se differentiation of lipsticks was possible on the basis of concentrations of trace elements and their profile. Concentration of bromine in samples of lipsticks identified lipsticks of different Indian brands. Samples of lipsticks of Indian and foreign brands could be differentiated on the basis of concentrations of cesium, antimony and scandium which were found to be higher in foreign brands as compared to those in Indian brands. (authors)

Standard test methods for chemical analysis of ceramic whiteware materials using wavelength dispersive X-Ray fluorescence spectrometry

CERN Document Server

American Society for Testing and Materials. Philadelphia

2004-01-01

1.1 These test methods cover the determination of ten major elements (SiO2, Al2O3, Fe2O3, MgO, CaO, Na2O, K2O, TiO2, P2O5, MnO, and LOI in ceramic whitewares clays and minerals using wavelength dispersive X-ray fluorescence spectrometry (WDXRF). The sample is first ignited, then fused with lithium tetraborate and the resultant glass disc is introduced into a wavelength dispersive X-ray spectrometer. The disc is irradiated with X-rays from an X-ray tube. X-ray photons emitted by the elements in the samples are counted and concentrations determined using previously prepared calibration standards. (1) In addition to 10 major elements, the method provides a gravimetric loss-on-ignition. Note 1—Much of the text of this test method is derived directly from Major element analysis by wavelength dispersive X-ray fluorescence spectrometry, included in Ref (1). 1.2 Interferences, with analysis by WDXRF, may result from mineralogical or other structural effects, line overlaps, and matrix effects. The structure of the...

TXRF, PIXE and EDXRF: a first step towards normalization of x-ray spectrometry for chemical analysis

International Nuclear Information System (INIS)

Barreiros, M.A.; Costa, M.M.; Palha, M.; Pinheiro, T.; Araujo, M.F.; Silva, R.C. da

2000-01-01

Nowadays, many research studies rely on analytical measurements to which x-ray spectrometry techniques are particularly adequate. Because they are multi-elemental, versatile, fast and can reach low detection limits they are often applied to environmental and biomedical studies. Besides, they are able to provide reliable and accurate results. As also occurs with other analytical procedures, the quality assurance for non-routine analysis in R and D laboratories, is much less well established. when compared with routine analytical work. Thus, it is of foremost importance, to set the major quality parameters that significantly affect the quality of results. In addition, there is a need to apply the new concepts of trace ability and uncertainty to these techniques. This work reports on the reliability of TXRF, PIXE and EDXRF measurements by evaluating the uncertainty and trace ability for elemental analysis. The set of experimental and statistical procedures used to ensure the quality of results relative to the proposed objectives, as well as the methods applied to estimate the uncertainties will be presented and discussed. The sample preparation procedures, analytical calibration and spectral evaluation will be the parameters examined in this inter-laboratory study. The sample preparation procedures comprise pressure acid digestion and pelletizing for solid samples. The internal quality control for analytical calibration and spectral analysis is performed using certified reference materials and standard solutions. The goal of this work is to present a first step towards normalization of x-ray spectrometry techniques for chemical analysis. (author)

Applications of gamma-ray spectrometry in real-time environmental monitoring

International Nuclear Information System (INIS)

Heath, R.L.; Dyer, N.C.

1974-01-01

The operation of large nuclear installations involves significant inventories of radioactive materials. Effective monitoring of effluent streams to permit evaluation of potential hazards which might result from discharge of radioisotopes is a requirement for safe operation of such facilities. The purpose of this paper is to present a summary of a program being conducted at the Idaho National Engineering Laboratory (INEL) to apply gamma-ray spectrometry to real-time isotopic monitoring of nuclear installations. The application of the lithium-drifted Ge spectrometer in the laboratory for isotopic assay is well established. To apply these techniques to routine on-line isotopic measurements requires the solution of a number of significant problems. These may be summarized as follows: the development of a remote pulse-height analyzer system; the development of adequate methods for analysis of pulse-amplitude spectra to permit isotopic assay and interpretation of results; and determination of basic nuclear decay data requirements for nuclides of interest to insure acceptance of isotopic assay results

Smoothing technology of gamma-ray spectrometry data based on matched filtering

International Nuclear Information System (INIS)

Gu Min; Ge Liangquan

2009-01-01

Traditional method of smoothness of gamma-ray spectrometry data gives rise to aberration of spectra curves easily. The article improve convolution sliding transformation using idea of matched filtering. Gauss adding the exponential function instead of Gauss function is used as converting function. The improved method not only suppresses statistical fluctuation mostly but also keeps feature of spectra curves. Instance verified superiority of this new method. (authors)

A new generation of x-ray spectrometry UHV instruments at the SR facilities BESSY II, ELETTRA and SOLEIL

Energy Technology Data Exchange (ETDEWEB)

Lubeck, J., E-mail: janin.lubeck@ptb.de; Fliegauf, R.; Holfelder, I.; Hönicke, P.; Müller, M.; Pollakowski, B.; Ulm, G.; Weser, J.; Beckhoff, B. [Physikalisch-Technische Bundesanstalt (PTB), Abbestr. 2-12, 10587 Berlin (Germany); Bogovac, M.; Kaiser, R. B.; Karydas, A. G.; Leani, J. J.; Migliori, A.; Sghaier, H. [Nuclear Science and Instrumentation Laboratory, IAEA Laboratories, A-2444, Seibersdorf (Austria); Boyer, B.; Lépy, M. C.; Ménesguen, Y. [CEA, LIST, Laboratoire National Henri Becquerel, Bât. 602 PC 111, CEA-Saclay 91191 Gif-sur-Yvette c. (France); Detlefs, B. [CEA-LETI, Minatec Campus, 17 rue des Martyrs, 38054 Grenoble (France); Eichert, D. [Elettra - Sincrotrone Trieste (EST) S.C.p.A., 34149 Basovizza, Trieste (Italy); and others

2016-07-27

A novel type of ultra-high vacuum instrument for X-ray reflectometry and spectrometry-related techniques for nanoanalytics by means of synchrotron radiation (SR) has been constructed and commissioned at BESSY II. This versa-tile instrument was developed by the PTB, Germany’s national metrology institute, and includes a 9-axis manipulator that allows for an independent alignment of the samples with respect to all degrees of freedom. In addition, it integrates a rotational and translational movement of several photodiodes as well as a translational movement of a beam-geometry-defining aperture system. Thus, the new instrument enables various analytical techniques based on energy dispersive X-ray detectors such as reference-free X-Ray Fluorescence (XRF) analysis, total-reflection XRF, grazing-incidence XRF, in addition to optional X-Ray Reflectometry (XRR) measurements or polarization-dependent X-ray absorption fine structure analyses (XAFS). Samples having a size of up to (100 × 100) mm{sup 2}; can be analyzed with respect to their mass deposition, elemental, spatial or species composition. Surface contamination, nanolayer composition and thickness, depth pro-file of matrix elements or implants, nanoparticles or buried interfaces as well as molecular orientation of bonds can be accessed. Three technology transfer projects of adapted instruments have enhanced X-Ray Spectrometry (XRS) research activities within Europe at the synchrotron radiation facilities ELETTRA (IAEA) and SOLEIL (CEA/LNE-LNHB) as well as at the X-ray innovation laboratory BLiX (TU Berlin) where different laboratory sources are used. Here, smaller chamber requirements led PTB in cooperation with TU Berlin to develop a modified instrument equipped with a 7-axis manipulator: reduced freedom in the choice of experimental geometry modifications (absence of out-of-SR-plane and reference-free XRS options) has been compensated by encoder-enhanced angular accuracy for GIXRF and XRR.

Characteristics of prepared gamma-ray calibration sources for radioactivity measurement of environmental and radiation control samples

International Nuclear Information System (INIS)

Samat, S.B.; Oi, Yoshihiro; Taki, Mitsumasa; Manabe, Iwao; Yoshida, Makoto; Minami, Kentaro

1995-03-01

Several types of calibration source having different density were prepared using one or combinations of those materials, namely foam cement, liquid, glass beads, polystyrene foam bead and hard plastic bead for gamma-ray spectrometry of the samples with different densities and shapes(variable height with constant base area). For each type of the source, a few sources were prepared to examine characteristics in such cases as (a) different heights but constant density, and (b) constant height and constant density. For the foam cement source, several sources with different densities and a constant height were prepared. All the sources were measured with a gamma-ray spectrometry system and the results were discussed. This report also presents the results obtained from the experiments for the evaluation of (1) the variation of detector efficiency-energy with gamma-ray energy, and (2) the variation of detector efficiency with density of the sources. (author)

Stress measurement by x-ray diffractometry

Energy Technology Data Exchange (ETDEWEB)

Mitchell, C M

1985-10-22

This invention relates to x-ray diffractometry and more particularly to apparatus and methods for the measurement of residual stress in polycrystalline, e.g. metallic, specimens. The procedure is based on measurement of the lattice strain of crystals by x-ray diffraction, in which change in the interplanar spacing of a set of crystal lattice planes due to strain causes a change in the diffraction angle of the scattered x-ray beam, from which latter change the magnitude of the strain can be determined. In a polycrystalline specimen, from well know relations for elastic behaviour in isotropic materials, the stress on a plane normal to a given direction in the surface has a component in the given direction which can be calculated from measurement of lattice strain in two directions in a plane containing the given direction and the normal to the specimen surface. In general three such stress components in three directions in the surface are required to determine the principal stresses and thus express the state of stress in the surface. (author). 2 tabs., 9 figs.

Developments in gamma-ray spectrometry: systems, software, and methods-II. 3. Low-Energy Gamma-Ray Spectrometry Using a Compton-Suppressed Telescope Detector

International Nuclear Information System (INIS)

Sigg, R.A.; DiPrete, D.P.

2001-01-01

The Savannah River Technology Center (SRTC) utilizes gamma-ray spectrometry in studying numerous areas of applied interest to the Savannah River Site (SRS). For example, analyses of long-lived gamma-ray-emitting fission products and actinides are required to meet waste characterization, process holdup, environmental restoration, and decontamination and decommissioning efforts. A significant portion of the overall effort centers on measurements of gamma rays having energies below several hundred kilo-electron-volts. To assist these efforts, the SRTC recently acquired a spectrometer system that provides lower natural and Compton scattered background levels while achieving relatively high counting efficiencies for low-energy gamma rays. The combination of high efficiency and low background provides factor-of- 2-to-4 improvements in minimum detectable activities and allows meeting programmatic objectives with shorter measurement times. Numerous Compton-suppression spectrometers have been reported since the concept was first advanced. The spectrometer consists of two high-purity germanium detectors in a telescope configuration surrounded by a background /Compton-suppression sodium iodide detector. The front germanium detector is a 20-mm-thick x 60-mm-diam broad energy spectrometer, and the rear detector is a 40% efficient 61- mm-diam x 60-cm-thick closed-end coaxial spectrometer. The cryostat housing the germanium detectors (a) includes a carbon composite window for transmitting low-energy gamma rays, (b) is in a J-type configuration to mask the germanium detectors from natural activities in the cryo-pumping media, and (c) is fabricated from materials selected for low background. The telescope detector is in the 8.6-cm-inside-diameter annulus of a 22.9- x 22.9-cm sodium iodide detector encased in a 10-cm-thick lead shield. The counting system is located in a basement counting room having ∼60-cm-thick concrete walls. Initial tests show that the low-energy segment of

Nondestructive analysis of silver in gold foil using synchrotron radiation X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Kasamatsu, Masaaki; Suzuki, Yasuhiro; Suzuki, Shinichi; Nakanishi, Toshio; Shimoda, Osamu; Nishiwaki, Yoshinori; Miyamoto, Naoki

2005-01-01

Small particles of gold foil detached from an indoor decoration might be important evidence to associate a suspect with a crime scene. We have investigated the application of elemental analysis using synchrotron radiation X-ray fluorescence spectrometry to discriminate small particles of gold foil. Eight kinds of gold foil samples collected in Japan were used in the experiments. As a result of synchrotron radiation X-ray fluorescence spectrometry, only two elements, gold and silver, were detected from all gold foil samples. The intensity ratios of AgK α /AuL α showed good correlation with the content ratios of Ag/Au. The variation of intensity ratio within a same sample was sufficiently small compared with those of different samples. Therefore the comparison of this intensity ratio can be an effective method to discriminate small particles originating from different types of gold foil. (author)

Use of Airborne Gamma-Ray Spectrometry in case of emergency. Example of HELGA exercise - collaboration between France and Germany

International Nuclear Information System (INIS)

Guillot, L.

2004-01-01

Since Chernobyl accident, airborne gamma-ray spectrometry has been recognised as a useful tool to evaluate consequences of an accident over large areas. Nine European countries have capabilities to perform such measurements. Between 1996 and 2003, a collaboration between these teams was supported by European community. In 2002, an exercise involving airborne and ground-based measurements was organised in Scotland. This exercise demonstrated the ability of European countries to provide assistance to one of them in case of emergency. Since this project has been completed, the French and German team decided to continue a collaboration. The CEA team (France) went in Germany in 2003 to participate to a survey with the German team. In September 2004, an exercise including mapping of contaminated areas and orphan sources search is planned in France. Such actions are good opportunities to exchange technical information about the acquisition systems and operating procedures. It is also essential to improve the availability of teams to obtain comparable and compatible results. The AGRS (airborne gamma ray spectrometry) systems involved in this exercise will be described and compared in this paper. The capacity of teams to work in collaboration in various situation (orphan source search, contamination mapping) will be then evaluated. In particular, a European Radiometric and Spectrometry format defined during Eccomags project will be used to create a database of raw and processed data. The aim is to produce quickly composite maps with data recorded by different teams. A choice of results will be presented and an assessment of capability of teams to work in collaboration will be done. (author)

Determination of impurities in magnesium and aluminium by X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Roca, M.; Diaz-Guerra, J.P.

1979-01-01

The determination of traces of Al, Cr, Cu, Fe, Mn, Ni, Pb, Si and of Bi, Cr, Cu, Fe, Ga, Mg, Mn, Ni, Pb, Si, Sn, Ti, V and Zn in samples of magnesium and aluminium, respectively, by means of X-ray fluorescence spectrometry, are studied. An automatic sequential spectrometer with an on-line computer for the treatment of data has been employed. The most suitable measurement parameters have been chosen for each element in order to achieve detection limits to a few p.p.m. For magnesium in the form of drillings the analyses are performed with satisfactory results for most impurities by pressing the samples into briquettes and employing metallic discs as standards. Correction methods for the spectral interferences of Ti on V, and V on Cr have been applied. (author)

The application of gamma-spectrometry to nuclear power plant (NPP) and environment

International Nuclear Information System (INIS)

Asgharizadeh, Farid.

1995-01-01

One of measuring systems is nuclear spectrometry, particularly Gamma-Ray Spectrometry, to measure and determine the radionuclide concentration within plant materials and environmental samples. There are four major applied techniques related to Nuclear Power Plant operation and environmental monitoring aspects. Some details about gamma ray spectrometry technique is discussed in chapter 2. The main emphasis is on the calculation of gamma-ray detector efficiency for different geometries, the minimum detectable activity concepts and dead-time correction. Also,some formula and relations are introduced. In chapter 3, the major applications of gamma-ray spectrometry for analysis of nuclear power plant and environmental samples are discussed. These applications are divided into four topics: Nuclear Fuel survey; based on the activity of fission products concentration in reactor coolant, two other applications are introduced: Fuel Burnup calculation and the calculation of rated activity of natural radionuclides in construction of materials which is the last and most important application: Measurement and determination of radionuclides activity concentr[[[[n in environmental samples is described through section 3.3 Sampling and measuring methods for research and monitoring aspects is evaluated. Some data about sample preparation methods such as pretreatment and solubilization procedures are presented. Quantitative chemical separations of trace constituents from complex sample materials invariably require meticulous work by an analytical chemist. The radiochemical separation deals with this subject. Instrumental aspects, relate to gamma-ray spectrometry, quality assurance, presentation and reporting of results are described. In the experimental part, determination of radionuclides concentration in sediment sample is presented

X ray and EUV spectroscopic measurements of highly charged tungsten ions relevant to fusion plasmas

International Nuclear Information System (INIS)

Radtke, R; Biedermann, C; Mandelbaum, P; Schwob, J L

2007-01-01

Using high-resolution x ray and extreme ultraviolet (EUV) spectrometry, the line emission of W 28+ - W 50+ ions was measured at the Berlin Electron Beam Ion Trap (EBIT). Our study encompasses a wide range of wavelengths (5-800 A) and includes the observation of electric and magnetic dipole lines. The results of our measurements are compared with predicted transition wavelengths from ab initioatomic structure calculations

Application of gamma ray spectrometry for evaluation of transfer factors in environmental matrices

International Nuclear Information System (INIS)

Rao, D.D.

2008-01-01

Gamma Ray Spectrometry (GRS) is performed using a variety of radiation detectors, to identify and determine radioactivity concentration of gamma emitting radionuclides qualitatively, in a wide range of samples. The samples can be of a high inventory power plant origin, NORM category or low level environmental samples, around a power plant. The method is usually applied to non-destructive analysis of environmental samples. However, it can also be applied to destructive analysis i.e. following extraction/separation of the analyte from the sample, if there is a need to pre-concentrate the analyte. The accuracy and precision of the method, depends on the quality of calibration, correction methods employed, stability of the system components, computational algorithms used, analysis of sources of uncertainties etc. The transfer factors among the environmental matrices are simple ratios, but the methodologies used in generating the respective concentrations have to be appropriately documented, including the validity of measurements. Validation mechanisms can include the results of international inter-comparison exercises, the certificates of standards issued by quality-accredited international laboratories. A few parameters involved in the qualitative analysis of gamma spectrometry are discussed here

Determination of U, Th and K in bricks by gamma -ray spectrometry, X-ray fluorescence analysis and neutron activation analysis

Czech Academy of Sciences Publication Activity Database

Bártová, H.; Kučera, Jan; Musílek, L.; Trojek, T.; Gregorová, E.

2017-01-01

Roč. 140, NOV (2017), s. 161-166 ISSN 0969-806X R&D Projects: GA MŠk LM2015056 Institutional support: RVO:61389005 Keywords : Gamma-ray spectrometry * neutron activation analysis * environmental dosimetry Subject RIV: CB - Analytical Chemistry , Separation OBOR OECD: Analytical chemistry Impact factor: 1.315, year: 2016

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

Energy Technology Data Exchange (ETDEWEB)

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

2010-02-15

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

X-ray fluorescence spectrometry and related techniques an introduction

CERN Document Server

Margui, Eva

2013-01-01

X-ray fluorescence spectrometry (XRF) is a well-established analytical technique for qualitative and quantitative elemental analysis of a wide variety of routine quality control and research samples. Among its many desirable features, it delivers true multi-element character analysis, acceptable speed and economy, easy of automation, and the capacity to analyze solid samples. This remarkable contribution to this field provides a comprehensive and up-to-date account of basic principles, recent developments, instrumentation, sample preparation procedures, and applications of XRF analysis. If you are a professional in materials science, analytic chemistry, or physics, you will benefit from not only the review of basics, but also the newly developed technologies with XRF. Those recent technological advances, including the design of low-power micro- focus tubes and novel X-ray optics and detectors, have made it possible to extend XRF to the analysis of low-Z elements and to obtain 2D or 3D information on a microme...

Several experimental applications of gamma ray spectrometry on the analysis of uranium compounds

International Nuclear Information System (INIS)

Korob, Ricardo O.; Blasiyh Nuno, Guillermo A.

2002-01-01

Several experimental applications of gamma ray spectrometry on the analysis of uranium compounds and materials containing it are studied. Special attention is devoted to the correlation between experimental spectra and the decay chains of 235 U and 238 U contained in the analyzed samples. The following applications are discussed: enrichment determination without using calibration standards, determination of uranium concentration, intensities of the gamma rays emitted by the nuclides present in the decay chains of study and the activity of such nuclides. Because of its importance, detailed discussion about the former one is shown. In addition, preliminary results regarding the emission probabilities of the most important gamma rays of 234m Pa are also informed. (author)

A low-energy set-up for gamma-ray spectrometry of NORM tailored to the needs of a secondary smelting facility

OpenAIRE

Lutter, Guilome; Vandael Schreurs, Indy; Croymans, Tom; Schroeyers, Wouter; Schreurs, Sonja; Hult, Mikael; Marissens, Gert; Stroh, Heiko; Tzikaa, Faidra

2017-01-01

A measurement station dedicated for quantitative radiological characterisation of naturally occurring radio-nuclides in a metallurgical company and based on gamma-ray spectrometry was developed. The station is intended for performing quality control of final non-ferrous metal products and for radiological checks of incoming materials. A low-background point-contact HPGe-detector was used and the signal was split in two branches to enable collecting simultaneously spectra with high amplificati...

Particle induced x-ray emission (PIXE) measurement of the Cd content in animal tissues

International Nuclear Information System (INIS)

Le Huong Quynh; Demeter, I.; Hollos-Nagy, K.; Szoekefalvi-Nagy, Z.

1989-12-01

Particle induced x-ray emission (PIXE) measurements were performed on thin samples prepared from different rabbit tissues, using 3 MeV proton beam for inducing x-rays from the animal tissues. This method is very sensitive and very small amounts of trace elements can be detected. Cadmium, one of the most toxic elements which can be concentrated in animal and human tissues due to environmental pollution, was detected with a limit of 0.7 ppm. The trace element concentrations obtained by PIXE were compared to those measured by atomic absorption spectrometry. PIXE method is proposed for routine analysis at the Veterinary and Food Investigating Service, Budapest, Hungary. (D.Gy.) 6 refs.; 3 figs

Thickness determination of thin solid films by angle-resolved X-ray fluorescence spectrometry using monochromatized synchrotron radiation

Science.gov (United States)

Schmitt, W.; Drotbohm, P.; Rothe, J.; Hormes, J.; Ottermann, C. R.; Bange, K.

1995-05-01

Thickness measurements by the method of angle-resolved, self-ratio X-ray fluorescence spectrometry (AR/SR/XFS) have been carried out on thin solid films using monochromatized synchrotron radiation at the Bonn storage ring ELSA. Synchrotron radiation was monochromatized by means of a double-crystal monochromator and fluorescence radiation was detected by a Si(Li) semiconductor detector. The results for sample systems consisting of Au on Si, Cr on SiO2 and TiO2 on alkali-free glass are very satisfactory and agree well with results obtained by other methods.

Porosity measurement of solid pharmaceutical dosage forms by gamma-ray transmission

International Nuclear Information System (INIS)

Martins de Oliveira, Jose; Andreo Filho, Newton; Vinicius Chaud, Marco; Angiolucci, Tatiana; Aranha, Norberto; Germano Martins, Antonio Cesar

2010-01-01

The aim of the present work is the determination of porosity in tablets by using the gamma-ray transmission technique. Tablet dissolution depends on some inherent characteristics of the manufacturing process, such as compression force, tablet volume, density and porosity, nature of excipients, preparation methods and its physical-chemical properties. Porosity is a measure of empty spaces in a material and can be determined by various techniques. In this paper, we propose the use of a gamma-ray transmission technique to obtain the porosity of experimental formulation of tablets. The results of porosity were compared with those obtained by using conventional methodology (density and mercury intrusion). The experimental setup for gamma-ray transmission consists of a gamma-ray source of 241 Am (photons of 59.6 keV and an activity of 3.7x10 9 Bq), an NaI(Tl) scintillation detector, collimators and a standard gamma-ray spectrometry electronics. Our results suggest that the gamma-ray transmission technique is a powerful tool for non-destructive porosity quantification of solid pharmaceutical forms and presents smaller errors than those obtained with conventional methodologies.

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

International Nuclear Information System (INIS)

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

2004-01-01

Two multielement instrumental methods of analysis, micro X-ray fluorescence spectrometry (micro-XRF) and inductively coupled plasma atomic emission spectrometry (ICP-AES) were applied for the analysis of 7th and 5th century B.C. ancient ceramic sherds in order to evaluate the above two methods and to assess the potential to use the current compact and portable micro-XRF instrument for the in situ analysis of ancient ceramics. The distinguishing factor of interest is that micro-XRF spectrometry offers the possibility of a nondestructive analysis, an aspect of primary importance in the compositional analysis of cultural objects. Micro-XRF measurements were performed firstly directly on the ceramic sherds with no special pretreatment apart from surface cleaning (micro-XRF on sherds) and secondly on pressed pellet disks which were prepared for each ceramic sherd (micro-XRF on pellet). For the ICP-AES determination of elements, test solutions were prepared by the application of a microwave-assisted decomposition procedure in closed high-pressure PFA vessels. Also, the standard reference material SARM 69 was used for the efficiency calibration of the micro-XRF instrument and was analysed by both methods. In order to verify the calibration, the standard reference materials NCS DC 73332 and SRM620 as well as the reference materials AWI-1 and PRI-1 were analysed by micro-XRF. Elemental concentrations determined by the three analytical procedures (ICP-AES, micro-XRF on sherds and micro-XRF on pellets) were statistically treated by correlation analysis and Student's t-test (at the 95% confidence level)

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

Energy Technology Data Exchange (ETDEWEB)

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

2004-12-01

Two multielement instrumental methods of analysis, micro X-ray fluorescence spectrometry (micro-XRF) and inductively coupled plasma atomic emission spectrometry (ICP-AES) were applied for the analysis of 7th and 5th century B.C. ancient ceramic sherds in order to evaluate the above two methods and to assess the potential to use the current compact and portable micro-XRF instrument for the in situ analysis of ancient ceramics. The distinguishing factor of interest is that micro-XRF spectrometry offers the possibility of a nondestructive analysis, an aspect of primary importance in the compositional analysis of cultural objects. Micro-XRF measurements were performed firstly directly on the ceramic sherds with no special pretreatment apart from surface cleaning (micro-XRF on sherds) and secondly on pressed pellet disks which were prepared for each ceramic sherd (micro-XRF on pellet). For the ICP-AES determination of elements, test solutions were prepared by the application of a microwave-assisted decomposition procedure in closed high-pressure PFA vessels. Also, the standard reference material SARM 69 was used for the efficiency calibration of the micro-XRF instrument and was analysed by both methods. In order to verify the calibration, the standard reference materials NCS DC 73332 and SRM620 as well as the reference materials AWI-1 and PRI-1 were analysed by micro-XRF. Elemental concentrations determined by the three analytical procedures (ICP-AES, micro-XRF on sherds and micro-XRF on pellets) were statistically treated by correlation analysis and Student's t-test (at the 95% confidence level)

A comparative study for the correction of random gamma ray summing effect in HPGe - detector based gamma ray spectrometry

International Nuclear Information System (INIS)

Rajput, M.U.

2007-01-01

Random coincidence summing of gamma rays is a potential source of errors in gamma ray spectrometry. The effect has a little significance at low counting rates but becomes increasingly important at high counting rates. Careful corrections are required to avoid the introduction of errors in quantitative based measurements. Several correction methods have been proposed. The most common is the pulser method that requires a precision Pulse Generator in the electronic circuitry to provide reference peak. In this work, a comparative study has been carried out both by using pulser method and utilizing radioactive source based method. This study makes the use of 137 Cs radionuclide as a fixed source and the 241 Am as a varied source. The dead time of the system has been varied and the acquisition of the spectra at each position yielded the resulted peak areas with pulsed pile up losses. The linear regression of the data has been carried out. The study has resulted in establishing a consistent factor that can be used as the characteristic of the detector and thereby removes the need of the calibrated or precise Pulse Generator. (author)

Improvement of sample preparation for input plutonium accountability measurement by isotope dilution gammy-ray spectroscopy

International Nuclear Information System (INIS)

Nishida, K.; Kuno, Y.; Sato, S.; Masui, J.; Li, T.K.; Parker, J.L.; Hakkila, E.A.

1992-01-01

The sample preparation method for the isotope dilution gamma-ray spectrometry (IDGS) technique has been further improved for simultaneously determining the plutonium concentration and isotopic composition of highly irradiated spent-fuel dissolver solutions. The improvement includes using ion-exchange filter papers (instead of resin beads, as in two previous experiments) for better separation and recovery of plutonium from fission products. The results of IDGS measurements for five dissolver solutions are in good agreement with those by mass spectrometry with ∼0.4% for plutonium concentration and ∼0.1% for 239 Pu isotopic composition. The precision of the plutonium concentration is ∼1% with a 1-h count time. The technique could be implemented as an alternative method for input accountability and verification measurements in reprocessing plants

OBT measurement of vegetation by mass spectrometry and radiometry

International Nuclear Information System (INIS)

Tamari, T.; Kakiuchi, H.; Momoshima, N.; Sugihara, S.; Baglan, N.; Uda, T.

2011-01-01

We carried out OBT (organically bound tritium) measurement by two different methods those are radiometry and mass spectrometry and compared the applicability of these methods for environmental tritium analysis. The dried grass sample was used for the experiments. To eliminate the exchangeable OBT, the sample was washed with tritium free water before analysis. Three times washing reduced the tritium activity in the labile sites below the detectable level. In radiometry the sample was combusted to convert the OBT as well as other hydrogen isotopes to. water and tritium activity in the water was measured by liquid scintillation counting (LSC). In mass spectrometry, the sample was kept in a glass container and 3 He produced by tritium decay was measured by mass spectrometry. The results were in good agreement suggesting applicability of these methods for environmental tritium analysis. The mass spectrometry is more suitable for environmental tritium research because of a lower detection limit than that of the LSC. (authors)

Assessing sample attenuation parameters for use in low-energy efficiency transfer in gamma-ray spectrometry

International Nuclear Information System (INIS)

Bruggeman, M.; Verheyen, L.; Vidmar, T.; Liu, B.

2016-01-01

We present a numerical fitting method for transmission data that outputs an equivalent sample composition. This output is used as input to a generalised efficiency transfer model based on the EFFTRAN software integrated in a LIMS. The procedural concept allows choosing between efficiency transfer with a predefined sample composition or with an experimentally determined composition based on a transmission measurement. The method can be used for simultaneous quantification of low-energy gamma emitters like "2"1"0Pb, "2"4"1Am, "2"3"4Th in typical environmental samples. - Highlights: • New fitting method for experimentally determined attenuation coefficients. • Generalised efficiency transfer with EFFTRAN based on transmission measurements. • Method of generalized efficiency transfer integrated in LIMS. • Method applicable to gamma-ray spectrometry of environmental samples.

The analysis of anode sludges by x-ray-fluorescence spectrometry

International Nuclear Information System (INIS)

Austen, C.E.; Wall, G.J.

1978-01-01

A method is described for the analysis, by X-ray-fluorescence spectrometry, of anode sludges for the determination of antimony, bismuth, copper, iron, lead, nickel, selenium, silver, tellurium, tin, and zinc. The preparation of the samples involves fusion with a flux of barium peroxide and lithium hydroxide, and with dichromium trioxide as the internal standard, in a zirconium or vitreous-carbon crucible and casting of the melt in an aluminium mould; the fused disc so formed is then pulverized and briquetted to form pellets. Calibration curves, which are straight lines for all the elemets determined because the flux contains a heavy absorber, are established by measurement of pellets prepared from standard anode sludges, pure metals, compounds of the metals, or any combination of these materials. The precision of the results varies between 2 and 15 per cent relative standard deviation, depending on the concentration of the element being determined. The accuracy of the results is comparable with that obtained by wet-chemical methods. The laboratory method is given in an appendix

Using airborne GAMMA-ray spectrometry (uranium, thorium, potassium) to quantify weathering and erosion processes

International Nuclear Information System (INIS)

Carrier, F.

2005-01-01

The airborne gamma-ray spectrometry survey carried out on the Armorican Massif provided soil contents in U, Th and K in ppm. Chemical and mechanical erosion processes within a homogeneous geological unit have been estimated using their variations and those of the 137 Cs. Our new approach, based on a multivariate analysis (hierarchic ascending classification), integrates the airborne gamma-ray spectrometry data, with their broad spatial distribution, together with precisely located station data (major elements, traces and isotopic geochemistry) resulting from a soil and river water erosion products survey. The total export of potassium was estimated in any point of an area catchment (50-m resolution) until 17+2 t/km 2 /a for a 50-m thick weathering profile. Erosion study by river sampling provide important biases, for the perennial river does not integrate the whole range of erosion products: the geochemical signature of the valleys is currently more represented than plateau areas. (author)

Field microcomputerized multichannel γ ray spectrometer based on notebook computer

International Nuclear Information System (INIS)

Jia Wenyi; Wei Biao; Zhou Rongsheng; Li Guodong; Tang Hong

1996-01-01

Currently, field γ ray spectrometry can not rapidly measure γ ray full spectrum, so a field microcomputerized multichannel γ ray spectrometer based on notebook computer is described, and the γ ray full spectrum can be rapidly measured in the field

Rare earth aerosol analysis by x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Citron, I.M.; Mausner, L.F.

1982-01-01

An analytical method for the determination of four lanthanides in air filter samples is described. The method involves simultaneous quantitative determinations of La, Ce, Pr, and Nd at the microgram level by x-ray fluorescence spectrometry without chemical separation of these rare earths and without serious interferences from the dust matrices on the filters. The method has been used successfully to analyze some air filter samples collected at a rare earth processing refinery in Illinois. A description of the development of the method is given as well as the results obtained by using this method on the air filter samples. The reproducibility of the results was generally +-5%

Single-Shot Spectrometry for X-Ray Free-Electron Lasers

International Nuclear Information System (INIS)

Yabashi, Makina; Ishikawa, Tetsuya; Hastings, Jerome B.; Zolotorev, Max S.; Mimura, Hidekazu; Yumoto, Hirokatsu; Matsuyama, Satoshi; Yamauchi, Kazuto

2006-01-01

An experimental scheme to realize single-shot spectrometry for the diagnostics of x-ray free-electron lasers (XFELs) is presented. The combination of an ultraprecisely figured mirror and a perfect crystal form a simple, high-precision spectrometer that can cover an energy range from a few eV to a hundred eV with high resolution. The application of the spectrometer to determine XFEL pulse widths was investigated theoretically and experimentally. It has been shown that the present system can determine pulse widths from sub-fs to ps in a single shot even for spontaneous radiation. The system can be easily extended to even shorter pulses

Measurement of the porosity of amorphous materials by gamma ray transmission methodology

International Nuclear Information System (INIS)

Pottker, Walmir Eno; Appoloni, Carlos Roberto

2000-01-01

In this work it is presented the measurement of the total porosity of TRe soil, Sandstone Berea rocks and porous ceramics samples. For the determination of the total porosity, the Arquimedes method (conventional) and the gamma ray transmission methodology were employed. The porosity measurement using the gamma methodology has a significant advantage respect to the conventional method due to the fast and non-destructive determination, and also for supplying results with a greater characterization in small scales, in relation to the heterogeneity of the porosity. The conventional methodology presents good results only for homogeneous samples. The experimental set up for the gamma ray transmission technique consisted of a 241 Am source (59,53 keV ), a NaI(Tl) scintillation detector, collimators, a XYZ micrometric table and standard gamma spectrometry electronics connected to a multichannel analyser. (author)

Elemental analysis of air particulate samples in Jakarta area by x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Yumiarti; Yusuf, M.; Mellawati, June; Menry, Yulizon; Surtipanti S

1998-01-01

Determination of elements in air particulate samples collected from Jakarta, especially from industrial area Pulo Gadung, also from residence, office, and recreation sites had been carried out. The samples collected periodically from August through December 1996. The elements were analyzed by X-ray fluorescence spectrometry method. Quantitative and qualitative analyses were done using QXAS AXIL (Quantitative X-ray Analysis System of x-ray Spectra by Iterative Least squares fitting) and QAES (Quantitative Analyses of Environmental Samples) package program. Results of the analyses showed that the content of heavy metal elements in air particulate samples from all areas studied were still below the maximum permissible concentration. (authors)

Simultaneous determination of RA-226, natural uranium and natural thorioum by gamma-ray spectrometry INa(Tl) in solid samples

International Nuclear Information System (INIS)

Salvador, S.; Navarro, T.; Alvarez, A.

1990-01-01

A method has been described to determine activities of Ra-226, natural uranium, and natural thorium, by gamma-ray spectrometry. The system was calibrated for efficiency by using synthetic calibrated standards. It is necessary, in the samples, to assume secular equilibrium between Ra-226 and Th-232 and its daughters nuclides, and U-238 and its immediate daughter Th-234, because the photopeaks measured are from these dsaugthers. Our results indicate that a non destructive gamma spectrometric method can ofter replace the radiochemical techniques used in measuring radiactivities in this type of samples. (Author). 9 refs

Humidity measurement using alpha-ray and beta-ray

International Nuclear Information System (INIS)

Matsumoto, Shigeaki; Kobayashi, Hisanobu

1981-01-01

Two new hygrometers using radioisotopes were proposed, and the results of tests are described. The one is a dew-point hygrometer utilizing the backscattering phenomena of beta-ray by dew, and the other is a hygrometer by measuring the variation of ionization current by alpha ray due to humidity. The backscattering of beta-ray depends on the atomic number of scatters and the energy of beta-ray. Therefore, the backscattering from dew on a gold plate is different from that from the gold itself. The temperature dependence of the backscattering intensity was measured with a GM counter. Decrease of the intensity was seen at the dew point. A control circuit was designed to measure the dew point automatically. The error of the measurement was within 1 degree C. An alpha-ray ionization hygrometer was constructed. The dependence of ionization current on humidity was measured with an operational amplifier. The resolution of humidity measurement was within 5 percent. (Kato, T.)

Applications of the Basic programming language in X-ray spectrometry

International Nuclear Information System (INIS)

Diaz-Guerra, J.P.; Roca, M.

1981-01-01

An assembly of programs written in ''Basic'' language and related with the calculation needs at the X-ray spectrometry laboratory of the Spanish J.E.N. has been developed. The principal problems considered, concerning the X-ray fluorescence technique, are the following: selection of the instrumental parameters; correction of the effects due to the dead time, background and spectral interferences; fitting of polynomial functions, which relate the variables intensity-concentration; application of some empirical-mathematical methods (Lucas-Tooth, Beattie and Brissey and Tertian procedures) to the correction of the inter-element effects; addition method, and statistical treatment of the results (correlation coefficient and ''F'' and ''t'' tests). Likewise, programs for the computation of spacings from powder diffraction patterns (Debye-Scherrer and counter diffractometer procedures) have been written. The proposed programs run following conversational patterns, in which different possibilities and incidences have been foreseen. (author)

Determination of carbon in natural freshwater biofilms with total reflection X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Ovari, M.; Streli, C.; Wobrauschek, P.; Zaray, Gy.

2009-01-01

There is a growing interest in determination of low Z elements, i.e., carbon to phosphorus, in biological samples. Total reflection X-ray fluorescence spectrometry (TXRF) has been already established as suitable trace element analytical method with low sample demand and quite good quantification limits. Recently, the determinable element range was extended towards Z = 6 (carbon). Biofilms can be used for biomonioring purposes in the aquatic environment. Besides the trace metals, especially the determination of the carbon content is important for the better understanding of the early stage of biofilm formation. For this, an ATI low Z spectrometer equipped with Cr-anode X-ray tube, multilayer monochromator, vacuum chamber, and a Si(Li) detector with ultra thin window was used. Biofilms were grown on two different artificial supports (granite and plexiglass), freeze dried, suspended in high purity water and analyzed. As an internal standard the natural titanium content of the biofilms was used. The accuracy of the method was checked by total carbon measurement using a combusting carbon analyzer.

Determination of carbon in natural freshwater biofilms with total reflection X-ray fluorescence spectrometry

Energy Technology Data Exchange (ETDEWEB)

Ovari, M. [Department of Analytical Chemistry, Eoetvoes University, Budapest, H-1117, Budapest, Pazmany Peter stny. 1/a. (Hungary)], E-mail: ovari@chem.elte.hu; Streli, C.; Wobrauschek, P. [Atominstitut of the Austrian Universities, TU-Wien, Stadionallee 2, A-1020, Wien (Austria); Zaray, Gy. [Department of Analytical Chemistry, Eoetvoes University, Budapest, H-1117, Budapest, Pazmany Peter stny. 1/a. (Hungary); Cooperative Research Centre of Environmental Chemistry, Eoetvoes University, Budapest, H-1117, Budapest, Pazmany Peter stny. 1/a. (Hungary)

2009-08-15

There is a growing interest in determination of low Z elements, i.e., carbon to phosphorus, in biological samples. Total reflection X-ray fluorescence spectrometry (TXRF) has been already established as suitable trace element analytical method with low sample demand and quite good quantification limits. Recently, the determinable element range was extended towards Z = 6 (carbon). Biofilms can be used for biomonioring purposes in the aquatic environment. Besides the trace metals, especially the determination of the carbon content is important for the better understanding of the early stage of biofilm formation. For this, an ATI low Z spectrometer equipped with Cr-anode X-ray tube, multilayer monochromator, vacuum chamber, and a Si(Li) detector with ultra thin window was used. Biofilms were grown on two different artificial supports (granite and plexiglass), freeze dried, suspended in high purity water and analyzed. As an internal standard the natural titanium content of the biofilms was used. The accuracy of the method was checked by total carbon measurement using a combusting carbon analyzer.

Final results of the PIDIE intercomparison exercise for the plutonium isotopic determination by gamma-ray spectrometry

International Nuclear Information System (INIS)

Morel, J.; Chauvenet, B.; Etcheverry, M.

1991-01-01

Final results from the PIDIE intercomparison exercise organised by the ESARDA Working Group on techniques and standards for non-destructive analysis are presented. The aim of this exercise carried out in 1988 was to test the gamma-ray spectroscopy methods used to determine the plutonium isotopic ratios in a large range of isotopic composition, in order to analyse the parameters and the error sources influencing the results. Sets of seven sealed samples of different plutonium isotopic composition were sent to nine participating laboratories. The final results with uncertainty indicators are reported; they are compared with complementary mass-spectrometry determinations. No important bias has been observed from this exercise. Significant improvements in plutonium isotopic determination by gamma-ray spectrometry come from both more elaborate spectrum analysis methods and better equipment

Validation of 226Ra, 228Ra and 210Pb measurements in soil and sediment samples through high resolution gamma ray spectrometry

International Nuclear Information System (INIS)

Dias, Danila Carrijo da Silva; Silva, Nivaldo Carlos da; Bonifacio, Rodrigo Leandro; Guerrero, Eder Tadeu Zenun

2013-01-01

Radionuclides found in ore extraction waste materials are a great source of concern regarding public health and environmental safety. One technique to determine the concentration of substances is high resolution gamma ray spectrometry using HPGe. Validating a measurement technique is essential to warrant high levels of quality to any scientific work. The Laboratory of Pocos de Caldas of the Brazilian Commission for Nuclear Energy partakes into a Quality Management System project, seeking Accreditation under ISO/IEC 17025 through the validation of techniques of chemical and radiometric analysis of environmental samples from water, soil and sediment. The focus of the Radon Laboratory at LAPOC is validation of Ra-226, Ra-228 and Pb-210 concentration determinations in soil and sediment through a gamma spectrometer system. The stages of this validation process included sample reception and preparation, detector calibration and sample analyses. Dried samples were sealed in metallic containers and analyzed after radioactive equilibrium between Ra-226 and daughters Pb-214 and Bi-214. Gamma spectrometry was performed using CANBERRA HPGe detector and gamma spectrum software Genie 2000. The photo peaks used for Ra-226 determination were 609 keV and 1020 keV of Bi-214 and 351 keV of Pb-214. For the Ra-228 determination a photopeak of 911 keV was used from its short half-life daughter Ac-228 (T1/2 = 6.12 h). For Pb-210, the photopeak of 46.5 keV was used, which, due to the low energy, self-absorption correction was needed. Parameters such as precision, bias/accuracy, linearity, detection limit and uncertainty were evaluated for that purpose. The results have pointed to satisfying results. (author)

Diagnostic x-ray spectra measurements using a silicon surface barrier detector

International Nuclear Information System (INIS)

Pani, R.; Laitano, R.F.

1987-01-01

A silicon surface barrier detector having a low efficiency for x-ray is used to analyse diagnostic x-ray spectra. This characteristic is advantageous in overcoming experimental problems caused by high fluence rates typical of diagnostic x-ray beams. The pulse height distribution obtained with silicon surface barrier detectors is very different from the true photon spectra because of the presence of escaped Compton photons and the fact that detection efficiency falls abruptly when photon energy increases. A detailed analysis of the spurious effects involved in detection is made by a Monte Carlo method. A stripping procedure is described for implementation on a personal computer. The validity of this method is tested by comparison with experimental results obtained with a Ge detector. The spectra obtained with the Si detector are in fairly good agreement with the analogous spectra measured with a Ge detector. The advantages of using Si as opposed to Ge detectors in x-ray spectrometry are: its simplicity of use, its greater economy for use in routine diagnostic x-ray spectroscopy and the possibility that the stripping procedure can be implemented on a personal computer. (author)

Analysis of spectra from portable handheld gamma-ray spectrometry for terrain comparative assessment

International Nuclear Information System (INIS)

Dias, Flávio; Lima, Marco; Sanjurjo-Sánchez, Jorge; Alves, Carlos

2016-01-01

Geological characteristics can have impacts on societal development by, e.g., geotechnical issues and radiological hazard levels. Due to urban sprawl, there is an increasing need for detailed geological assessment. In this work are analysed data from portable handheld gamma-ray spectra (K, eU and eTh) obtained in granitic and Silurian metaclastic outcrops as well as in an profile, roughly N–S, on soil covered terrains transecting a mapped contact between these rock types (the profile's northern extremity is at locations mapped as granite). Estimations from gamma-ray spectra were studied by univariate and multivariate analyses. K, eU and eTh values were higher on granite in relation to Silurian metaclastic rocks. The northern extremity of the profile showed clearly higher contents of eTh and this contrast was supported by univariate statistical tools (normality plot and Wilk–Shapiro test; boxplots). A ternary plot with the contribution of the elements to gamma-ray absorbed dose showed the separation of granite from Silurian metaclastic rocks with the former being nearer the eTh vertex. The points in the northern extremity of the profile are nearer the eTh vertex than the other points on the profile. These visual suggestions were supported by hierarchical cluster analysis, which was able to differentiate between granite and metaclastic outcrops and separate portions of the profile located on different terrains. Portable gamma-ray spectrometry showed, hence, the potential to distinguish granite and metaclastic terrains at a scale useful for engineering works. These results can also be useful for a first comparative zoning of radiological hazards (which are higher for granite). - Highlights: • Contents of K, eU and eTh were estimated by portable gamma-ray spectra. • Spectra were acquired on a profile across a soil covered granite/metaclastic contact. • Spectra were also collected on granite and Silurian metaclastic outcrops. • Obtained estimations were

Comparison of different mass spectrometry techniques in the measurement of L-[ring-13C6]phenylalanine incorporation into mixed muscle proteins

Science.gov (United States)

Zabielski, Piotr; Ford, G. Charles; Persson, X. Mai; Jaleel, Abdul; Dewey, Jerry D.; Nair, K Sreekumaran

2013-01-01

Precise measurement of low enrichment of stable isotope labeled amino-acid tracers in tissue samples is a prerequisite in measuring tissue protein synthesis rates. The challenge of this analysis is augmented when small sample size is a critical factor. Muscle samples from human participants following an 8 hour intravenous infusion of L-[ring-13C6]phenylalanine and a bolus dose of L-[ring-13C6]phenylalanine in a mouse were utilized. Liquid Chromatography tandem mass spectrometry (LC/MS/MS), Gas Chromatography tandem mass spectrometry (GC/MS/MS) and Gas Chromatography/Mass spectrometry (GC/MS) were compared to the Gas Chromatography-Combustion-Isotope Ratio mass spectrometry (GC/C/IRMS), to measure mixed muscle protein enrichment of [ring13C6]phenylalanine enrichment. The sample isotope enrichment ranged from 0.0091 to 0.1312 Molar Percent excess (MPE). As compared with GC/C/IRMS, LC/MS/MS, GC/MS/MS and GC/MS showed coefficients of determination of R2 = 0.9962 and R2 = 0.9942, and 0.9217 respectively. However, the precision of measurements (coefficients of variation) for intra-assay are 13.0%, 1.7%, 6.3% and 13.5% and for inter-assay are 9.2%, 3.2%, 10.2% and 25% for GC/C/IRMS, LC/MS/MS, GC/MS/MS and GC/MS respectively. The muscle sample sizes required to obtain these results were 8μg, 0.8μg, 3μg and 3μg for GC/C/IRMS, LC/MS/MS, GC/MS/MS, and GC/MS respectively. We conclude that LC/MS/MS is optimally suited for precise measurements of L-[ring-13C6]phenylalanine tracer enrichment in low abundance and in small quantity samples. PMID:23378099

The combined measurement of uranium by alpha spectrometry and secondary ion mass spectrometry (SIMS)

International Nuclear Information System (INIS)

Harvan, D.

2009-01-01

The aim of thesis was to found the dependence between radiometric method - alpha spectrometry and surface sensitive method - Secondary Ion Mass Spectrometry (SIMS). Uranium or naturally occurring uranium isotopes were studied. Samples (high polished stainless steel discs) with uranium isotopes were prepared by electrodeposition. Samples were measured by alpha spectrometry after electrodeposition and treatment. It gives surface activities. Weights, as well as surface's weights of uranium isotopes were calculated from their activities, After alpha spectrometry samples were analyzed by TOF-SIMS IV instrument in International Laser Centre in Bratislava. By the SIMS analysis intensities of uranium-238 were obtained. The interpretation of SIMS intensities vs. surface activity, or surface's weights of uranium isotopes indicates the possibility to use SIMS in quantitative analysis of surface contamination by uranium isotopes, especially 238 U. (author)

Gamma-ray spectrometry data collection and reduction by simple computing systems

International Nuclear Information System (INIS)

Op de Beeck, J.

1975-01-01

The review summarizes the present state of the involvement of relatively small computing devices in the collection and processing of gamma-ray spectrum data. An economic and utilitarian point of view has been chosen with regard to data collection in order to arrive at practically valuable conclusions in terms of feasibility of possible configurations with respect to their eventual application. A unified point of view has been adopted with regard to data processing by developing an information theoretical approach on a more or less intuitive level in an attempt to remove the largest part of the virtual disparity between the several processing methods described in the literature. A synoptical introduction to the most important mathematical methods has been incorporated, together with a detailed theoretical description of the concept gamma-ray spectrum. In accordance with modern requirements, the discussions are mainly oriented towards high-resolution semiconductor detector-type spectra. The critical evaluation of the processing methods reviewed is done with respect to a set of predefined criteria. Smoothing, peak detection, peak intensity determination, overlapping peak resolving and detection and upper limits are discussed in great detail. A preferred spectrum analysis method combining powerful data reduction properties with extreme simplicity and speed of operation is suggested. The general discussion is heavily oriented towards activation analysis application, but other disciplines making use of gamma-ray spectrometry will find the material presented equally useful. Final conclusions are given pointing to future developments and shifting their centre of gravity towards improving the quality of the measurements rather than expanding the use of tedious and sophisticated mathematical techniques requiring the limits of available computational power. (author)

Airborne radon-222 measurement by active sampling with charcoal adsorption and gamma-ray spectrometry

International Nuclear Information System (INIS)

Shizuma, Kiyoshi; Wen, Xiao-qiong; Fukami, Kenji; Iwatani, Kazuo; Hamanaka, Shun-ichi

1998-01-01

A simple method for measuring radon concentration in air is presented. Airborne radon is adsorbed in a charcoal bed by an active air sampling. In time, the adsorbed radon comes to attain radioactive equilibrium with its short-lived progeny 214 Pb. Utilizing this fact, radon concentration is derived from γ-ray measurement of 214 Pb. This method is estimated to be capable of detecting radon concentration in air down to 0.79 Bq·m -3 . The adsorption coefficient obtained with the method is compared with what is obtainable with passive sampling. Applications of this method to indoor and outdoor radon measurements are described. (author)

High-z semiconductor nuclear radiation detectors for room-temperature gamma-ray spectrometry

International Nuclear Information System (INIS)

Bornand, Bernard; Friant, Alain.

1978-09-01

A bibliographical review (182 articles of periodicals, conferences, reports, thesis and french patents) is presented, as addendum of the report CEA-BIB-210 (1974) on high-Z semiconductor compounds used as materials for the gamma and X-ray detection and spectrometry. This publication reviews issues from 1974 to 1977. References and summaries (in french) are incorporated into 182 bibliograhical notices. Index for authors, corporate authors, documents and periodicals, and subjects is included [fr

INTERACTION OF ALBUMIN AND IMMUNOGLOBULIN G WITH SYNTHETIC HYDROXYAPATITE

Directory of Open Access Journals (Sweden)

E. Pylypchuk

2012-12-01

Full Text Available It was shown by X-ray phase analysis, IR spectra analysis and MALDI-ToF mass spectrometry methods that interaction of synthetic hydroxyapatite with a solution of immunoglobulin G leads to its partial dissolution due to leaching from the surface of calcium triphosphate which, in our opinion, forms complexes with immunoglobulin G.

Velocity-space sensitivity of neutron spectrometry measurements

DEFF Research Database (Denmark)

Jacobsen, Asger Schou; Salewski, Mirko; Eriksson, J.

2015-01-01

Neutron emission spectrometry (NES) measures the energies of neutrons produced in fusion reactions. Here we present velocity-space weight functions for NES and neutron yield measurements. Weight functions show the sensitivity as well as the accessible regions in velocity space for a given range...

Simultaneous determination of Ra-226, natural uranium and natural thorium by gamma-ray spectrometry INa(Ti), in solid samples

International Nuclear Information System (INIS)

Salvador, S.; Navarro, T.; Alvarez, A.

1991-01-01

A method has been developed to determine activities of Ra-226, natural uranium and natural thorium by gamma-ray spectrometry. The measurement system has been calibrated using standards specially prepared at the laboratory. It is necessary to assume secular equilibrium in the samples, between Ra-226 and Th-232 and its daughters nuclides, and between U-238 and its immediate daughter Th-234, as the photo peaks measured are those of the daughters. The results obtained indicate that this method can of ter replace the radiochemical techniques used to measure activities in this type of sample. The method has been successfully used to determine these natural isotopes in samples from uranium mills. (Author) 9 refs

X-ray hot plasma diagnostics

International Nuclear Information System (INIS)

Cojocaru, E.

1984-11-01

X-ray plasma emission study is powerful diagnostic tool of hot plasmas. In this review article the main techniques of X-ray plasma emission measurement are shortly presented: X-ray spectrometry using absorbent filters, crystal and grating spectrometers, imaging techniques using pinhole cameras, X-ray microscopes and Fresnel zone plate cameras, X-ray plasma emission calorimetry. Advances in these techniques with examples for different hot plasma devices are also presentes. (author)

A strategy for vitrification product assurance and control with X-ray fluorescence spectrometry (PACX)

International Nuclear Information System (INIS)

Resce, J.L.

1995-01-01

A product control strategy is proposed for the vitrification of low-level and/or mixed waste. This strategy is called Product Assurance and Control with X-ray fluorescence spectrometry (PACX). The strategy utilizes sequential wavelength dispersive x-ray fluorescence spectrometry and standardless fundamental parameters calculations to analyze both the melter feed and the glassy products. The melter feed is sampled prior to addition to the melt tank and then melted and cast into samples which should closely resemble the product from the vitrification process itself. The resulting sample disks are then analyzed by x-ray fluorescence spectrometry. All elements with atomic numbers down to sodium can be determined directly and then either boron or lithium can be determined by difference from the mass balance. The XRF intensities are converted into oxide compositions with the use of a novel standardless fundamental parameters program. Previous work has shown that there is an excellent correlation between the XRF results and the results from conventional wet chemical analyses, but the XRF results can be obtained within two to three hours of sampling. If compositional control limits for durability are available, the product acceptability can be determined prior to the batch being introduced into the melter. The durability could also be estimated from a model, if available, which predicts product durability from composition. If the predicted durability is estimated to be too low, the model can then be used to determine additives which will raise the durability of the final product to within acceptable limits. The additives can then be incorporated into the batch prior to addition into the melter. A similar XRF analysis can be carried out on the glass product from the melter which can then be used to predict and thus assure product acceptance

Preliminary Determination of Natural Radioactivity Levels of the State of Qatar using High-Resolution Gamma-ray Spectrometry

International Nuclear Information System (INIS)

Al-Sulaiti, H.A.; Regan, P.H.; Bradley, D.A.; Matthews, M.; Santawamaitre, T.; Malain, D.

2009-01-01

The State of Qatar is a peninsula with a total area of 11,437 km 2 which lies over a geological formation comprising a sequence of limestone, chalk, clay and gypsum. Establishing a baseline for the radioactivity concentration in Qatar's soil is the main purpose behind the present study. The project is focused on obtaining measurements of representative soil samples from various areas in Qatar to establish concentrations of the 235 U, 238 U and 232 Th natural decay chains and also the long-lived naturally occurring radionuclide 40 K. The 235 U, 238 U, 232 Th and 40 K concentrations have been measured via high-resolution gamma-ray spectrometry using a hyper-pure germanium detector situated in a low-background environment with a copper inner-plated passive lead shield. A wide range of different gamma-ray energy transitions lines arising from the multiple decay products from the 235 U, 238 U and 232 Th decay chains have been analyzed separately to obtain more statistically significant overall results

Analysis of selected elements in tobacco by wavelength dispersive X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Martin, J.M.

1988-01-01

A rapid method for the determination of 16 elements in tobacco by wavelength dispersive X-ray fluorescence spectrometry has been developed. The method is accurate and precise, and requires only 9 min per sample for quantitation. Sample preparation consists of placing a portion of dried, ground tobacco in a sample cup, and pressing at 25 tons pressure to make a compressed pellet. This pellet is then automatically analyzed by X-ray fluorescence for 16 elements. The results are stored on a computer disk for future recall and report generation. The elements are: Al, Br, Ca, Cl, Cu, Fe, K, Mg, Mn, Na, P, S, Si, Sr, Ti and Zn

Thin coating thickness determination using radioisotope-excited x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Del Castillo, Lorena A.; Calix, Virginia S.

2001-01-01

Three different approaches on thin coating thickness determination using a radioisotope-excited x-ray fluorescence spectrometry were demonstrated and results were compared. A standard of thin layer of gold (Au) on a nickel (Ni) substrate from the US National Bureau of Standards (with a nominal thickness of 0.300505 microns of at least 99.9% Au electrodeposited over 2 nils of Ni) on low carbon steel (1010) was analyzed using a Cd 109-excited XRF system. Au thickness computations were done using the (a) thin standard approach, (b) thick standard approach, and (c) x-ray absorption method (ASTM A754-79 1982). These three methods yielded results within the limit set by the American Society for Testing Materials (ASTM), which is +/-3%. Of the three methods, the thick standard yielded the best result with 0.124% error. (Author)

A double cell for X-ray absorption spectrometry of atomic Zn

CERN Document Server

Mihelic, A; Arcon, I; Padeznik-Gomilsek, J; Borowski, M

2002-01-01

A high-temperature cell with a double wall design has been constructed for X-ray absorption spectrometry of metal vapors. The inner cell, assembled from a corundum tube and thin plates without welding or reshaping, serves as a container of the vapor sample. It is not vacuum tight: instead, the outer tube provides inert atmosphere. Several spectra of K-edge atomic absorption of Zn were obtained in the stationary working regime below the Zn boiling point. The K-edge profile shows an extremely strong resonance and, above the continuum threshold, coexcitations of the outer electrons.

Quantitative analysis of phosphosilicate glass films on silicon wafers for calibration of x-ray fluorescence spectrometry standards

International Nuclear Information System (INIS)

Weissman, S.H.

1983-01-01

The phosphorus and silicon contents of phosphosilicate glass films deposited by chemical vapor deposition (CVD) on silicon wafers were determined. These films were prepared for use as x-ray fluorescence (XRF) spectrometry standards. The thin films were removed from the wafer by etching with dilute hydrofluoric acid, and the P and Si concentrations in solution were determined by inductively coupled plasma atomic emission spectroscopy (ICP). The calculated phosphorus concentration ranged from 2.2 to 12 wt %, with an uncertainty of 2.73 to 10.1 relative percent. Variation between the calculated weight loss (summation of P 2 O 5 and SiO 2 amounts as determined by ICP) and the measured weight loss (determined gravimetrically) averaged 4.9%. Results from the ICP method, Fourier transform-infrared spectroscopy (FT-IR), dispersive infrared spectroscopy, electron microprobe, and x-ray fluorescence spectroscopy for the same samples are compared

Trace-element analysis of uranium ores by x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Coetzee, P.P.; De Villiers, W.v Z.

1985-01-01

The determination of seventeen trace elements (As, Ba, Co, Cr, Cu, Mo, Nb, Ni, Pb, Sr, Th, U, V, Y, Zn, and Zr) in uranium ores by x-ray fluorescence spectrometry was investigated. For the elements with analyte lines in the vicinity of the U-L lines, large overlap corrections were necessary and only a few completely interference-free background positions were available. Consequently, the Feather and Willis method was used for determining the background intensity at the peak positions as well as mass absorption coefficients. As a result of the presence of the U-L absorption edges, both primary and secondary mass absorption coefficients had to be used for matrix corrections. Furthermore, it was observed that the background intensity in the region of the uranium lines increased with increasing uranium content of the sample, instead of the expected decrease due to the increasing mass absorption coefficient. This was attributed to the scattering of uranium lines in the spectrometer chamber. A method was developed to correct the measured intensities for this effect. The contribution from the scattering of uranium lines to the measured intensity at the various 20 positions was determined on samples with different uranium concentrations and for which the mass absorption coefficients and concentrations of the various elements were known

Developments in gamma-ray spectrometry: systems, software, and methods-II. 4. High-Performance Digital Gamma-Ray Spectrometry

International Nuclear Information System (INIS)

Michael Momayezi

2001-01-01

This paper reviews recent advances in the field of digital spectrometry made by researchers at X-Ray Instrumentation Associates. All XIA spectrometers are based on a core architecture, which employs digitizing the input signal without shaping and applying all basic data processing in real time to the digital data stream coming out of the wave form digitizer. The real-time digital data processing includes filtering, triggering, pileup rejection, and even pulse shape analysis. In this paper we will describe some of those methods that go beyond emulating a conventional analog system in a digital environment. Rather we will concentrate mainly on methods that have no real equivalent in the analog world. In conventional spectrometers pulse pileup recognition is hardwired and serves a single purpose, namely to reject signals that occur too close to each other to allow for a precise measurement of their amplitude. For a digital device, which can also record wave forms, that would be an unfortunate limitation. The study of very short-lived radioactive isotopes is a case in point. If such an isotope is implanted into a detector in which it then decays by charged particle emission, the signature for the sought-after isotope is that of an implant pulse followed by one or more decay pulses from the isotope and its daughters. If the decay products can be absorbed in the same detector channel, as is the case for proton and alpha emitters in a Si-strip detector, then the isotope decay will show up as a pulse train coming from that detector channel. The difficulty usually is to find the few isotopes of interest amongst a huge background of long-lived or stable isotopes. With programmable pileup recognition logic it is possible to trigger specifically on pulse trains, rather than single pulses, thereby picking out very selectively the isotopes of interest. Analyzing the pulse shape of the incoming preamplifier signal proves to be very useful in many applications. The most obvious

X-ray measurements on wood - spectra measurements

DEFF Research Database (Denmark)

Jensen, Signe Kamp; Thygesen, Lisbeth Garbrecht; Gerward, Leif

The report concerns simultaneous non-destructive measurements of water content and density of wood. Theoretically, this should be possible using a x-ray equipment newly build at BKM, and this work is an attempt to use the equipment for assessing water content and density of wood samples under...... laboratory conditions. A number of wood samples with different densities are placed at different relative humidities from 0.5 to 97 %RH. When equilibrium is obtained the samples are measured with the x-ray equipment such that 10 points are measured in the sample followed by measurements outside the sample...... (free-scanning). In this way 100 points are measured for each wood sample. This produces information about moisture content and density of the samples as water and wood attenuations of the x-rays are different for the different energy levels contained in the x-rays. The "real" density and moisture...

KRAS G12C Drug Development: Discrimination between Switch II Pocket Configurations Using Hydrogen/Deuterium-Exchange Mass Spectrometry

Energy Technology Data Exchange (ETDEWEB)

Lu, Jia; Harrison, Rane A.; Li, Lianbo; Zeng, Mei; Gondi, Sudershan; Scott, David; Gray, Nathanael S.; Engen, John R.; Westover, Kenneth D. (NEU); (DFCI); (UTSMC); (Harvard-Med)

2017-09-01

KRAS G12C, the most common RAS mutation found in non-small-cell lung cancer, has been the subject of multiple recent covalent small-molecule inhibitor campaigns including efforts directed at the guanine nucleotide pocket and separate work focused on an inducible pocket adjacent to the switch motifs. Multiple conformations of switch II have been observed, suggesting that switch II pocket (SIIP) binders may be capable of engaging a range of KRAS conformations. Here we report the use of hydrogen/deuterium-exchange mass spectrometry (HDX MS) to discriminate between conformations of switch II induced by two chemical classes of SIIP binders. We investigated the structural basis for differences in HDX MS using X-ray crystallography and discovered a new SIIP configuration in response to binding of a quinazoline chemotype. These results have implications for structure-guided drug design targeting the RAS SIIP.

Comparative studies for determining U-235/U-238 relation in solutions of natural and depleted uranium using gamma spectrometry and neutron activation analysis

International Nuclear Information System (INIS)

Cassorla F, V.; Valle M, L.; Pena V, L.

1988-01-01

Two experimental methods were developed for determining U-235/U-238 ratio in uranium solutions. The isotopic was measured by high resolution ratio gamma-ray spectrometry (G.S.) and neutron activation analysis (N.A.A.). The precision obtained was similar for both methods, but better sensitivity was obtained by N.A.A. The accuracy in both cases was stablished by comparison with samples previously analyzed by mass spectrometry, the results were satisfactory for both techniques. Studies involving the influence of the nitric acid concentration on the isotopic ratio measurement, also were done. In addition, computer programs for faster data reduction were developped, in the case of N.A.A. (author)

Dispersive liquid–liquid microextraction using diethyldithiocarbamate as a chelating agent and the dried-spot technique for the determination of Fe, Co, Ni, Cu, Zn, Se and Pb by energy-dispersive X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Kocot, Karina; Zawisza, Beata; Sitko, Rafal

2012-01-01

Dispersive liquid–liquid microextraction (DLLME) using sodium diethyldithiocarbamate (DDTC) as a chelating agent was investigated for the simultaneous determination of iron, cobalt, nickel, copper, zinc, selenium and lead ions in water samples. The procedure was performed using 5 mL of the sample, 100 μL of a 0.5% solution of DDTC, 30 μL of carbon tetrachloride (extraction phase) and 500 μL of methanol (disperser solvent). The experiments showed that Fe, Co, Ni, Cu, Zn and Pb can be simultaneously extracted at a pH of 5 and that Se can be extracted at a pH of 2–3. The results were compared with those obtained using ammonium pyrrolidine dithiocarbamate as a chelating agent. For all analytes, a linear range was observed up to 0.4 μg mL −1 . If Fe and Zn are present in concentrations 10 times higher than those of the other analytes, then the linearity is observed up to 0.2 μg mL −1 . In the present study, the organic phase that contained preconcentrated elements was deposited onto a Millipore filter and measured using energy-dispersive X-ray fluorescence spectrometry. The obtained detection limits were 2.9, 1.5, 2.0, 2.3, 2.5, 2.0 and 3.9 ng mL −1 for Fe, Co, Ni, Cu, Zn, Se and Pb, respectively. This combination of DLLME and the dried-spot technique is promising for multielement analyses using other spectroscopy techniques, such as laser ablation‐inductively coupled plasma‐mass spectrometry, laser-induced breakdown spectroscopy or total-reflection X-ray fluorescence spectrometry. - Highlights: ► Multielement trace analysis using dried-spot technique and dispersive liquid–liquid microextraction. ► Possibility of combination of LPME with EDXRF, LIBS or LA-ICP-MS. ► Comparison of APDC and DDTC as chelating agents.

New technique for determination of long-lived radioisotopes, Iodine-129, using multiparameter coincidence spectrometry

International Nuclear Information System (INIS)

Hatsukawa, Yuichi; Oshima, Masumi; Toh, Yosuke; Shinohara, Nobuo; Kushita, Kosuke; Ueno, Takashi

2003-01-01

Multiparameter coincidence γ-ray spectrometry based on g-g coincidence is widely used in the field of nuclear structure studies, and has produced many successful results. In this study, feasibility of the method for neutron activation analysis of long lived iodine isotope, 129 I, was investigated. (author)

Multivariate statistical approximation of the in situ gamma-ray spectrometry of the State of Zacatecas, Mexico

International Nuclear Information System (INIS)

Lopez I, J. F.; Rios M, C.; Mireles G, F.; Saucedo A, S.; Davila R, I.; Pinedo, J.L.

2017-09-01

The environmental radioactivity evaluation is a key point in the assessment of the environmental quality. Through this, it can be found possible radioactive contamination, locate possible Uranium and Thorium deposits and evaluate the primordial isotopes concentration due to human activities. A radioactive map of the Zacatecas State, Mexico is under construction based on in situ gamma-ray spectrometry. The present work reports the results of the multivariate statistical approximation of the measured activity data. Based on Pearson correlation, the 228 Ac and 208 Tl activities are statistically significant, while the 214 Bi and 214 Pb activities are not statistically significant. These can be due to the existence or not of secular equilibrium in the Thorium and Uranium series. (Author)

Specialized software utilities for gamma ray spectrometry. Final report of a co-ordinated research project 1996-2000

International Nuclear Information System (INIS)

2002-03-01

A Co-ordinated Research Project (CRP) on Software Utilities for Gamma Ray Spectrometry was initiated by the International Atomic Energy Agency in 1996 for a three year period. In the CRP several basic applications of nuclear data handling were assayed which also dealt with the development of PC computer codes for various spectrometric purposes. The CRP produced several software packages: for the analysis of low level NaI spectra; user controlled analysis of gamma ray spectra from HPGe detectors; a set of routines for the definition of the detector resolution function and for the unfolding of experimental annihilation spectra; a program for the generation of gamma ray libraries for specific applications; a program to calculate true coincidence corrections; a program to calculate full-energy peak efficiency calibration curve for homogenous cylindrical sample geometries including self-attenuation correction; and a program for the library driven analysis of gamma ray spectra and for the quantification of radionuclide content in samples. In addition, the CRP addressed problems of the analysis of naturally occurring radioactive soil material gamma ray spectra, questions of quality assurance and quality control in gamma ray spectrometry, and verification of the expert system SHAMAN for the analysis of air filter spectra obtained within the framework of the Comprehensive Nuclear Test Ban Treaty. This TECDOC contains 10 presentations delivered at the meeting with the description of the software developed. Each of the papers has been indexed separately

Study on the Effects of Sample Density on Gamma Spectrometry System Measurement Efficiency at Radiochemistry and Environment Laboratory

International Nuclear Information System (INIS)

Wo, Y.M.; Dainee Nor Fardzila Ahmad Tugi; Khairul Nizam Razali

2015-01-01

The effects of sample density on the measurement efficiency of the gamma spectrometry system were studied by using four sets multi nuclide standard sources of various densities between 0.3 - 1.4 g/ ml. The study was conducted on seven unit 25 % coaxial HPGe detector gamma spectrometry systems in Radiochemistry and Environment Laboratory (RAS). Difference on efficiency against gamma emitting radionuclides energy and measurement systems were compared and discussed. Correction factor for self absorption caused by difference in sample matrix density of the gamma systems were estimated. The correction factors are to be used in quantification of radionuclides concentration in various densities of service and research samples in RAS. (author)

Portable gamma-ray holdup and attributes measurements of high- and variable-burnup plutonium

International Nuclear Information System (INIS)

Wenz, T.R.; Russo, P.A.; Miller, M.C.; Menlove, H.O.; Takahashi, S.; Yamamoto, Y.; Aoki, I.

1991-01-01

High burnup-plutonium holdup has been assayed quantitatively by low resolution gamma-ray spectrometry. The assay was calibrated with four plutonium standards representing a range of fuel burnup and 241 Am content. Selection of a calibration standard based on its qualitative spectral similarity to gamma-ray spectra of the process material is partially responsible for the success of these holdup measurements. The spectral analysis method is based on the determination of net counts in a single spectral region of interest (ROI). However, the low-resolution gamma-ray assay signal for the high-burnup plutonium includes unknown amounts of contamination from 241 Am. For most needs, the range of calibration standards required for this selection procedure is not available. A new low-resolution gamma-ray spectral analysis procedure for assay of 239 Pu has been developed. The procedure uses the calculated isotope activity ratios and the measured net counts in three spectral ROIs to evaluate and remove the 241 Am contamination from the 239 Pu assay signal on a spectrum-by-spectrum basis. The calibration for the new procedure requires only a single plutonium standard. The procedure also provides a measure of the burnup and age attributes of holdup deposits. The new procedure has been demonstrated using portable gamma-ray spectroscopy equipment for a wide range of plutonium standards and has also been applied to the assay of 239 Pu holdup in a mixed oxide fuel fabrication facility. 10 refs., 5 figs., 3 tabs

X-ray fluorescence analysis and optical emission spectrometry of an roman mirror from Tomis, Romania

International Nuclear Information System (INIS)

Belc, M.; Bogoi, M.; Ionescu, D.; Guita, D.; Caiteanu, S.; Caiteanu, D.

2000-01-01

The miscellaneous population of Roman Empire, their diverse cultural tradition, their ability to assimilate the roman civilization spirits, had determined a permanent reassessment superimposed upon the roman contribution. Analysis was undertaken using optical emission spectrometry and non-destructive X-ray fluorescence. X-ray fluorescence analysis is a well-established method and is often used in archaeometry and other work dealing with valuable objects pertaining to the history of art and civilization. Roman mirror analysed has been found not to be made of speculum (a high tin bronze). (authors)

Development of Total Reflection X-ray fluorescence spectrometry quantitative methodologies for elemental characterization of building materials and their degradation products

Science.gov (United States)

García-Florentino, Cristina; Maguregui, Maite; Marguí, Eva; Torrent, Laura; Queralt, Ignasi; Madariaga, Juan Manuel

2018-05-01

In this work, a Total Reflection X-ray fluorescence (TXRF) spectrometry based quantitative methodology for elemental characterization of liquid extracts and solids belonging to old building materials and their degradation products from a building of the beginning of 20th century with a high historic cultural value in Getxo, (Basque Country, North of Spain) is proposed. This quantification strategy can be considered a faster methodology comparing to traditional Energy or Wavelength Dispersive X-ray fluorescence (ED-XRF and WD-XRF) spectrometry based methodologies or other techniques such as Inductively Coupled Plasma Mass Spectrometry (ICP-MS). In particular, two kinds of liquid extracts were analysed: (i) water soluble extracts from different mortars and (ii) acid extracts from mortars, black crusts, and calcium carbonate formations. In order to try to avoid the acid extraction step of the materials and their degradation products, it was also studied the TXRF direct measurement of the powdered solid suspensions in water. With this aim, different parameters such as the deposition volume and the measuring time were studied for each kind of samples. Depending on the quantified element, the limits of detection achieved with the TXRF quantitative methodologies for liquid extracts and solids were set around 0.01-1.2 and 2-200 mg/L respectively. The quantification of K, Ca, Ti, Mn, Fe, Zn, Rb, Sr, Sn and Pb in the liquid extracts was proved to be a faster alternative to other more classic quantification techniques (i.e. ICP-MS), accurate enough to obtain information about the composition of the acidic soluble part of the materials and their degradation products. Regarding the solid samples measured as suspensions, it was quite difficult to obtain stable and repetitive suspensions affecting in this way the accuracy of the results. To cope with this problem, correction factors based on the quantitative results obtained using ED-XRF were calculated to improve the accuracy of

Scanning electron microscopy-energy dispersive X-ray spectrometry (SEM-EDX) and aerosol time-of-flight mass spectrometry (ATOFMS) single particle analysis of metallurgy plant emissions.

Science.gov (United States)

Arndt, J; Deboudt, K; Anderson, A; Blondel, A; Eliet, S; Flament, P; Fourmentin, M; Healy, R M; Savary, V; Setyan, A; Wenger, J C

2016-03-01

The chemical composition of single particles deposited on industrial filters located in three different chimneys of an iron-manganese (Fe-Mn) alloy manufacturing plant have been compared using aerosol time-of-flight mass spectrometry (ATOFMS) and scanning electron microscopy-energy dispersive X-ray spectrometry (SEM-EDX). Very similar types of particles were observed using both analytical techniques. Calcium-containing particles dominated in the firing area of the sintering unit, Mn and/or Al-bearing particles were observed at the cooling area of the sintering unit, while Mn-containing particles were dominant at the smelting unit. SEM-EDX analysis of particles collected downstream of the industrial filters showed that the composition of the particles emitted from the chimneys is very similar to those collected on the filters. ATOFMS analysis of ore samples was also performed to identify particulate emissions that could be generated by wind erosion and manual activities. Specific particle types have been identified for each emission source (chimneys and ore piles) and can be used as tracers for source apportionment of ambient PM measured in the vicinity of the industrial site. Copyright © 2015 Elsevier Ltd. All rights reserved.

Application of simulated standard spectra in natural radioactivity measurements using gamma spectrometry

International Nuclear Information System (INIS)

Narayani, K.; Pant, A.D.; Bhosle, Nitin; Anilkumar, S.; Singh, Rajvir; Pradeepkumar, K.S.

2014-01-01

Gamma ray spectrometry is one of the well known analytical techniques for environmental radioactivity measurements. Gamma spectrometer based on NaI(Tl) scintillation detectors is very popular since it offers high efficiency, low cost and case in handling. The poor energy resolution of the NaI(TI) detector is the major disadvantage making tile analysis of complex gamma ray spectra difficult. Least square method or the full spectrum analysis method is widely used for the analysis of complex spectra from scintillation detectors. The main requirement of this method is that the individual standard spectra of all nuclides expected in the complex spectrum in the same measurement geometry must be available. It is not always possible and feasible to have all the standards of nuclides in the desired geometry. A methodology based on the use of simulated standard spectra generated by Monte Carlo technique was proposed for analysis of complex spectra of nuclides. In the present work, for the analysis of 238 U, 233 Th and 40 K in soil samples, the same methodology was applied by using the simulated standard spectra in soil matrix. The details of the simulation method and results analysis of 238 U, 232 Th and 40 K in environmental samples are discussed in this paper

A differential mobility spectrometry/mass spectrometry platform for the rapid detection and quantitation of DNA adduct dG-ABP.

Science.gov (United States)

Kafle, Amol; Klaene, Joshua; Hall, Adam B; Glick, James; Coy, Stephen L; Vouros, Paul

2013-07-15

There is continued interest in exploring new analytical technologies for the detection and quantitation of DNA adducts, biomarkers which provide direct evidence of exposure and genetic damage in cells. With the goal of reducing clean-up steps and improving sample throughput, a Differential Mobility Spectrometry/Mass Spectrometry (DMS/MS) platform has been introduced for adduct analysis. A DMS/MS platform has been utilized for the analysis of dG-ABP, the deoxyguanosine adduct of the bladder carcinogen 4-aminobiphenyl (4-ABP). After optimization of the DMS parameters, each sample was analyzed in just 30 s following a simple protein precipitation step of the digested DNA. A detection limit of one modification in 10^6 nucleosides has been achieved using only 2 µg of DNA. A brief comparison (quantitative and qualitative) with liquid chromatography/mass spectrometry is also presented highlighting the advantages of using the DMS/MS method as a high-throughput platform. The data presented demonstrate the successful application of a DMS/MS/MS platform for the rapid quantitation of DNA adducts using, as a model analyte, the deoxyguanosine adduct of the bladder carcinogen 4-aminobiphenyl. Copyright © 2013 John Wiley & Sons, Ltd.

Inference of the phase-to-mechanical property link via coupled X-ray spectrometry and indentation analysis: Application to cement-based materials

Energy Technology Data Exchange (ETDEWEB)

Krakowiak, Konrad J.; Wilson, William [Department of Civil and Environmental Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139-4307 (United States); James, Simon [Schlumberger Riboud Product Center, 1 Rue Henri Becquerel, Clamart 92140 (France); Musso, Simone [Schlumberger-Doll Research Center, 1 Hampshire St., Cambridge, MA 02139-1578 (United States); Ulm, Franz-Josef, E-mail: ulm@mit.edu [Department of Civil and Environmental Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139-4307 (United States)

2015-01-15

A novel approach for the chemo-mechanical characterization of cement-based materials is presented, which combines the classical grid indentation technique with elemental mapping by scanning electron microscopy-energy dispersive X-ray spectrometry (SEM-EDS). It is illustrated through application to an oil-well cement system with siliceous filler. The characteristic X-rays of major elements (silicon, calcium and aluminum) are measured over the indentation region and mapped back on the indentation points. Measured intensities together with indentation hardness and modulus are considered in a clustering analysis within the framework of Finite Mixture Models with Gaussian component density function. The method is able to successfully isolate the calcium-silica-hydrate gel at the indentation scale from its mixtures with other products of cement hydration and anhydrous phases; thus providing a convenient means to link mechanical response to the calcium-to-silicon ratio quantified independently via X-ray wavelength dispersive spectroscopy. A discussion of uncertainty quantification of the estimated chemo-mechanical properties and phase volume fractions, as well as the effect of chemical observables on phase assessment is also included.

Deuterium measurement by emission spectrometry

International Nuclear Information System (INIS)

Niemann, E.G.; Heilig, K.; Dumke, I.

1978-01-01

The method makes it possible to determine the relative deuterium content of enriched water samples. For this, the relative intensities of the Hα and Dα lines are measured which are emitted by a high-frequency discharge in water vapour. Although the method is not as exact as mass spectrometry, it has the following advantages: - Easy sample preparation (no reduction necessary); - samples of highly different enrichment can be measured one after the other without the danger of memory effects; - much lower apparatus and cost expenditure. The necessary sample size is about the same in both methods. (orig.) [de

Open-source implementation of an algorithm for photopeaks search and analysis in gamma-ray spectrometry with semiconductor detectors

International Nuclear Information System (INIS)

Maduar, Marcelo F.; Pecequilo, Brigitte R.S.

2009-01-01

Radioactivity quantification of gamma-ray emitter radionuclides in samples measured by HPGe gamma spectrometers relies on the analysis of the photopeaks present in the spectra, especially on the accurate determination of their net areas. This paper presents a methodology and an algorithm description for the peak search and analysis in order to obtain the relevant peaks parameters and their uncertainties. The procedure is performed on a three step approach: a preliminary search is done by using the second-difference method; experimental peaks widths are assessed in order to obtain a width vs. channel relationship and to define regions with single or overlapping peaks; a non-linear fit is applied to each region of the spectrum with candidate peaks. The final target function is in the form G(x) = B(x) + F(x), where B(x) is the baseline composed by a sum of a weighed left-side B L (x) and right-side B R (x) base-line quadratic functions and the photopeaks term F(x) is a sum of Gaussian functions. The computational implementation is released entirely in open-source license. The code was developed in C++ language and the interface was developed with Qt GUI software toolkit. GNU scientific library, GSL, was employed to perform linear and non-linear fitting procedures as needed. Spectra previously generated at our laboratories were analyzed with the presented methodology and with the commercial software package WinnerGamma. Results obtained are consistent with those obtained with the aforementioned package, suggesting that it could be safely used in general-purpose gamma-ray spectrometry. (author)

Determination of sulphur with total reflection x-ray spectrometry

International Nuclear Information System (INIS)

Steinmeyer, S.; Kolbesen, B.O.

2000-01-01

The potential and limitations of total reflection x-ray spectrometry (TXRF) were tested for the quantitative determination of the light element sulphur in inorganic and biological samples. As representatives of inorganic samples alkali, transition metal, magnesium and aluminum sulphates were investigated. As biological samples the sulphur containing amino acid methionine and the pharmaceutical drug insulin were chosen. All measurements were performed on a TXRF-spectrometer EXTRA IIA (Atomika Instruments, Oberschleissheim/Germany) using tungsten L-radiation as the excitation tube. Various concentrations of all samples ranging from 20 mg/l to 0.5 mg/l were determined. In addition the surface topography and thickness of the dry residue of these samples were investigated with SEM and a thickness profilometer (Alpha-Step). The result show that the reliable determination of sulphur in sulphates depends on the cation involved. Alkali sulphates like Na 2 SO 4 , or K 2 SO 4 form bulky residues resulting in significant deviations of the recovery rate of sulphur. In this case the use of smoothing detergents like 1 % HF, 1 % malic acid and 2 % hydrazinhydrat was found to be necessary for accurate determination. The results for the biological samples agree well with the expected values. The investigations lead to the conclusion that TXRF combined with a proper samples preparation is well suited for the determination of sulphur in different samples with various concentrations and matrices. (author)

A method for the complete analysis of NORM building materials by γ-ray spectrometry using HPGe detectors.

Science.gov (United States)

Quintana, B; Pedrosa, M C; Vázquez-Canelas, L; Santamaría, R; Sanjuán, M A; Puertas, F

2018-04-01

A methodology including software tools for analysing NORM building materials and residues by low-level gamma-ray spectrometry has been developed. It comprises deconvolution of gamma-ray spectra using the software GALEA with focus on the natural radionuclides and Monte Carlo simulations for efficiency and true coincidence summing corrections. The methodology has been tested on a range of building materials and validated against reference materials. Copyright © 2017 Elsevier Ltd. All rights reserved.

Investigation of polyelectrolytes by total reflection x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Varga, I.; Nagy, M.

2000-01-01

Water soluble polyelectrolyte samples containing mono-, bi- and trivalent metal ions were investigated without any pretreatment. Acid digestion of linear polymers may lead to a product insoluble in water so the digestion has to be avoided. The aim of this paper was the determination of analytical characteristics and limitations of the total reflection x-ray fluorescence (TXRF) analysis for poly (vinylalcohol-vinylsulphate) salts and poly (acrylic acid, acrylamide) copolymers containing the following cations: K + , Cs + , Ba 2+ , Cu 2+ and La 3+ . On the basis of our results efficiency of ion-exchange during preparation of polyelectrolytes and stoichiometry of the end-product were determined. TXRF results were compared with data gained by inductively coupled plasma atomic emission spectrometry (ICP-AES) measurements except in the case of Cs + which has poor sensitivity in ICP-AES. Good agreement was found between the results of the two techniques and calculations from titrimetric data. Concentration of Li + and Mg 2+ in polymer samples was measured by ICP-AES. In majority of cases film-like dry residues of aqueous solutions of polyelectrolytes can be characterized by homogeneous spatial distribution of metal ions within the organic matrix. This is because the migration of the ions is hindered during drying process. Determination of metals in polyelectrolyte films by TXRF is quite ideal as model for analysis of plant, animal or human tissues which is a frequent task in environmental and inorganic biomedical analytical chemistry. (author)

Application of x-ray fluorescence to the measurement of additives in paper

International Nuclear Information System (INIS)

Buchnea, A.; McNelles, L.A.; Sinclair, A.H.; Hewitt, J.S.

1976-01-01

Titanium dioxide content in paper was measured by x-ray fluorescence analysis using an 55 Fe source and an x-ray proportional counter to determine the feasibility of an on-line instrument. X-ray calibration curves for 60- and 100-g/m 2 paper samples were obtained using neutron activation to measure the titanium dioxide concentration. The predictions of a simple model were in good agreement with the experimental calibration curves. The measurements and calculations were extended to investigate the effects of clay and moisture. The presence of clay has a significant effect on the x-ray fluorescence determination of the titanium dioxide concentration; however, this can be well accounted for by the model. The calculations indicated that the effect of typical moisture levels on the titanium dioxide determination was small and can be ignored. It is not possible to measure the clay content by x-ray fluorescence; however, preliminary results for the determination of calcium carbonate concentration are promising

Pu abundances, concentrations, and isotopics by x- and gamma-ray spectrometry assay techniques

International Nuclear Information System (INIS)

Camp, D.C.; Gunnink, R.; Ruhter, W.D.; Prindle, A.L.; Gomes, R.J.

1986-01-01

Two x- and gamma-ray systems were recently installed at-line in gloveboxes and will measure Pu solution concentrations from 5 to 105 g/L. These NDA technique, developed and refined over the past decade, are now used domestically and internationally for nuclear material process monitoring and accountability needs. In off- and at-line installations, they can measure solution concentrations to 0.2%. The K-XRFA systems use a transmission source to correct for solution density. The gamma-ray systems use peaks from 59- to 208-keV to determine solution concentrations and relative isotopics. A Pu check source monitors system stability. These two NDA techniques can be combined to form a new, NDA measurement methodology. With the instrument located outside of a glovebox, both relative Pu isotopics and absolute Pu abundances of a sample located inside a glovebox can be measured. The new technique works with either single or dual source excitation; the former for a detector 6 to 20 cm away with no geometric corrections needed; the latter requires geometric corrections or source movement if the sample cannot be measured at the calibration distance. 4 refs., 7 figs., 2 tabs

Determination of non-ionic surfactants in technologic liquors and effluents by X-ray fluorescent spectrometry

International Nuclear Information System (INIS)

Dankowski, P.; Majda, J.

1977-01-01

The method has been worked out for determination of non-ionic surfactants in technological liquors and effluents, based on the X-ray fluorescent spectrometry with an initial concentration by means of the phosphomolybdic acid. The method is suitable for a quantitative determination of ethylene oxide adducts in a wide range of applicable concentrations, the trace-ones included. (M.Z.)

Optimization of a neural network model for signal-to-background prediction in gamma-ray spectrometry

International Nuclear Information System (INIS)

Dragovic, S.; Onjia, A. . E-mail address of corresponding author: sdragovic@inep.co.yu; Dragovic, S.)

2005-01-01

The artificial neural network (ANN) model was optimized for the prediction of signal-to-background (SBR) ratio as a function of the measurement time in gamma-ray spectrometry. The network parameters: learning rate (α), momentum (μ), number of epochs (E) and number of nodes in hidden layer (N) were optimized simultaneously employing variable-size simplex method. The most accurate model with the root mean square (RMS) error of 0.073 was obtained using ANN with online backpropagation randomized (OBPR) algorithm with α = 0.27, μ 0.36, E = 14800 and N = 9. Most of the predicted and experimental SBR values for the eight radionuclides ( 226 Ra, 214 Bi, 235 U, 40 K, 232 Th, 134 Cs, 137 Cs and 7 Be), studied in this work, reasonably agreed to within 15 %, which was satisfactory accuracy. (author)

Affinity selection-mass spectrometry and its emerging application to the high throughput screening of G protein-coupled receptors.

Science.gov (United States)

Whitehurst, Charles E; Annis, D Allen

2008-07-01

Advances in combinatorial chemistry and genomics have inspired the development of novel affinity selection-based screening techniques that rely on mass spectrometry to identify compounds that preferentially bind to a protein target. Of the many affinity selection-mass spectrometry techniques so far documented, only a few solution-based implementations that separate target-ligand complexes away from unbound ligands persist today as routine high throughput screening platforms. Because affinity selection-mass spectrometry techniques do not rely on radioactive or fluorescent reporters or enzyme activities, they can complement traditional biochemical and cell-based screening assays and enable scientists to screen targets that may not be easily amenable to other methods. In addition, by employing mass spectrometry for ligand detection, these techniques enable high throughput screening of massive library collections of pooled compound mixtures, vastly increasing the chemical space that a target can encounter during screening. Of all drug targets, G protein coupled receptors yield the highest percentage of therapeutically effective drugs. In this manuscript, we present the emerging application of affinity selection-mass spectrometry to the high throughput screening of G protein coupled receptors. We also review how affinity selection-mass spectrometry can be used as an analytical tool to guide receptor purification, and further used after screening to characterize target-ligand binding interactions, enabling the classification of orthosteric and allosteric binders.

Assessment of the equilibrium of Th-228 and Ra-228 by gamma-ray spectrometry in mangrove soils

International Nuclear Information System (INIS)

Paiva, Jose Daniel S.; Farias, Emerson E.G.; Franca, Elvis J. De

2015-01-01

The mangrove environment consists of soil containing high organic matter, characterized by the influence of continental and oceanic waters, relatively high concentrations of salts and exuberant vegetation. Mangroves also present high dynamics of chemical compound cycling, in which soils become quite relevant due to the influence of continental and oceanic sediments. Taking into account the different sources and transport of radionuclides within the mangrove environment, this study focused at the radioactive equilibrium of Thorium-232 series radionuclides, especially the Ra-228 and Thorium-228. For this, soil samples were collected in the crown projection of tree species from two mangroves located in the municipalities of Olinda/Recife and Rio Formoso, Pernambuco State, Brazil. The material was oven-dried and milled and test portions of 38 g were transferred to cylindrical vials and sealed. After 30 days, the natural radioactivity was measured during 80,000 seconds using High Resolution Gamma-Ray Spectrometry with a germanium detector of 2.2 keV of resolution at the 1,332 keV Co-60 photopeak. For Ra-228 determination, 911 keV gamma-ray line (Ac-228) were employed, while 238 keV (Pb-212) and 727 keV (Bi-212) were considered for estimating activity concentrations of Th-228. As a result, Ra-228 and Th 228 were in equilibrium since the activity concentrations (ranging from 35 Bq/kg to 50 Bq/kg) were not significantly different at the 95% confidence level. The results have confirmed that, even for environments of high dynamics such as mangroves, radioactive equilibrium of Th-228 and Ra-228 was kept, corroborating Th-232 determination in mangrove soils. (author)

Assessment of the equilibrium of Th-228 and Ra-228 by gamma-ray spectrometry in mangrove soils

Energy Technology Data Exchange (ETDEWEB)

Paiva, Jose Daniel S.; Farias, Emerson E.G.; Franca, Elvis J. De, E-mail: paivajds@gmail.com, E-mail: emersonemiliano@yahoo.com.br, E-mail: ejfranca@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil)

2015-07-01

The mangrove environment consists of soil containing high organic matter, characterized by the influence of continental and oceanic waters, relatively high concentrations of salts and exuberant vegetation. Mangroves also present high dynamics of chemical compound cycling, in which soils become quite relevant due to the influence of continental and oceanic sediments. Taking into account the different sources and transport of radionuclides within the mangrove environment, this study focused at the radioactive equilibrium of Thorium-232 series radionuclides, especially the Ra-228 and Thorium-228. For this, soil samples were collected in the crown projection of tree species from two mangroves located in the municipalities of Olinda/Recife and Rio Formoso, Pernambuco State, Brazil. The material was oven-dried and milled and test portions of 38 g were transferred to cylindrical vials and sealed. After 30 days, the natural radioactivity was measured during 80,000 seconds using High Resolution Gamma-Ray Spectrometry with a germanium detector of 2.2 keV of resolution at the 1,332 keV Co-60 photopeak. For Ra-228 determination, 911 keV gamma-ray line (Ac-228) were employed, while 238 keV (Pb-212) and 727 keV (Bi-212) were considered for estimating activity concentrations of Th-228. As a result, Ra-228 and Th 228 were in equilibrium since the activity concentrations (ranging from 35 Bq/kg to 50 Bq/kg) were not significantly different at the 95% confidence level. The results have confirmed that, even for environments of high dynamics such as mangroves, radioactive equilibrium of Th-228 and Ra-228 was kept, corroborating Th-232 determination in mangrove soils. (author)

Radioactivity measurements in soils surrounding four coal-fired power plants in Serbia by gamma-ray spectrometry and estimated dose

Directory of Open Access Journals (Sweden)

Vukašinović Ivana Ž.

2014-01-01

Full Text Available The study of spatial distribution of activity concentration of 238U, 226Ra, 210Pb, 232Th, 40K, and 137Cs radionuclides in the surface soil samples (n = 42 collected in the vicinity of four coal-fired power plants in Serbia is presented. Radioactivity measurements in soils performed by gamma-ray spectrometry showed values [Bqkg-1] in the range: 15-117 for 238U, 21-115 for 226Ra, 33-65 for 210Pb, 20-69 for 232Th, 324-736 for 40K, and 2-59 for 137Cs. Surface soil radio-activity that could have resulted from deposition of radionuclides from airborne discharges or resuspension of ash from disposal sites showed no enhanced levels. It was found that variation of soil textural properties, pH values, and carbonate content influenced activity levels of natural radionuclides while radiocesium activities were associated with soil organic matter content. Modification of some soil properties was observed in the immediate vicinity (<1 km of power plants where the soil was more alkaline with coarser particles (0.2-0.05 mm and carbonates accumulated. Calculated average values of the absorbed gamma dose rate and annual external effective dose originating from the terrestrial radionuclides were 69.4 nGy/h and 0.085 mSv, respectively. [Projekat Ministarstva nauke Republike Srbije, br. 4007: Studying climate change and its influence on the environment: impacts, adaptation and mitigation

Analysis of total and dissolved heavy metals in surface water of a Mexican polluted river by total reflection X-ray fluorescence spectrometry

Energy Technology Data Exchange (ETDEWEB)

Zarazua, G. [Instituto Nacional de Investigaciones Nucleares, Gerencia de Ciencias Ambientales, Apartado Postal 18-1027, Mexico D.F., C.P. 11801 (Mexico)]. E-mail: gzo@nuclear.inin.mx; Avila-Perez, P. [Instituto Nacional de Investigaciones Nucleares, Gerencia de Ciencias Ambientales, Apartado Postal 18-1027, Mexico D.F., C.P. 11801 (Mexico); Tejeda, S. [Instituto Nacional de Investigaciones Nucleares, Gerencia de Ciencias Ambientales, Apartado Postal 18-1027, Mexico D.F., C.P. 11801 (Mexico); Barcelo-Quintal, I. [Universidad Autonoma Metropolitana, Unidad Azcapotzalco, Mexico, D.F. (Mexico); Martinez, T. [Universidad Nacional Autonoma de Mexico, Facultad de Quimica, Mexico, D.F. (Mexico)

2006-11-15

The present area of study is located in the Upper Course of the Lerma River (UCLR). The Lerma is one of the most important rivers of Mexico, where it drains highly populated and industrialized regions. The aim of the present study is to determine the heavy metal concentration of Cr, Mn, Fe, Cu and Pb in dissolved and total phases of the UCLR by means of Total Reflection X-ray Fluorescence Spectrometry (TXRF). The surface water samples were collected at 8 sites distributed following the stream flow direction of the river. Four sampling campaigns were carried out in each site in a 1-year period. A sample preparation method was applied in order to obtain the total and dissolved fraction and to destroy the organic matter. The total heavy metal average concentration decrease in the following order: Fe (2566 {mu}g/L) > Mn (300 {mu}g/L) > Cu (66 {mu}g/L) > Cr (21 {mu}g/L) > Pb (15 {mu}g/L). In general, the heavy metal concentrations in water of the UCLR are below the maximum permissible limits.

Analysis of total and dissolved heavy metals in surface water of a Mexican polluted river by total reflection X-ray fluorescence spectrometry

Science.gov (United States)

Zarazua, G.; Ávila-Pérez, P.; Tejeda, S.; Barcelo-Quintal, I.; Martínez, T.

2006-11-01

The present area of study is located in the Upper Course of the Lerma River (UCLR). The Lerma is one of the most important rivers of Mexico, where it drains highly populated and industrialized regions. The aim of the present study is to determine the heavy metal concentration of Cr, Mn, Fe, Cu and Pb in dissolved and total phases of the UCLR by means of Total Reflection X-ray Fluorescence Spectrometry (TXRF). The surface water samples were collected at 8 sites distributed following the stream flow direction of the river. Four sampling campaigns were carried out in each site in a 1-year period. A sample preparation method was applied in order to obtain the total and dissolved fraction and to destroy the organic matter. The total heavy metal average concentration decrease in the following order: Fe (2566 μg/L) > Mn (300 μg/L) > Cu (66 μg/L) > Cr (21 μg/L) > Pb (15 μg/L). In general, the heavy metal concentrations in water of the UCLR are below the maximum permissible limits.

Analysis of total and dissolved heavy metals in surface water of a Mexican polluted river by total reflection X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Zarazua, G.; Avila-Perez, P.; Tejeda, S.; Barcelo-Quintal, I.; Martinez, T.

2006-01-01

The present area of study is located in the Upper Course of the Lerma River (UCLR). The Lerma is one of the most important rivers of Mexico, where it drains highly populated and industrialized regions. The aim of the present study is to determine the heavy metal concentration of Cr, Mn, Fe, Cu and Pb in dissolved and total phases of the UCLR by means of Total Reflection X-ray Fluorescence Spectrometry (TXRF). The surface water samples were collected at 8 sites distributed following the stream flow direction of the river. Four sampling campaigns were carried out in each site in a 1-year period. A sample preparation method was applied in order to obtain the total and dissolved fraction and to destroy the organic matter. The total heavy metal average concentration decrease in the following order: Fe (2566 μg/L) > Mn (300 μg/L) > Cu (66 μg/L) > Cr (21 μg/L) > Pb (15 μg/L). In general, the heavy metal concentrations in water of the UCLR are below the maximum permissible limits

Thorium determination by x-ray fluorescence spectrometry in simulated thorex process solutions

International Nuclear Information System (INIS)

Yamaura, M.; Matsuda, H.T.

1991-11-01

The X-ray fluorescence method for thorium determination in aqueous and organic (TBP/n-dodecane) solutions is described. The thin film technique for sample preparation and a suitable internal standard had been used. The best conditions for Thorium determination had been established studying some parameters as analytical line, internal standard, filter paper, paper geometry, sample volume and measurement conditions. With the established conditions, thorium was concentration range of to 200 g Th/L and in organic solutions (2-63g Th/L) with 1,5% of precision. The accuracy of the proposed method was 3% in aqueous and organic phases. The detection limit was 1,2μg thorium for aqueous solutions and 1,4μg for organic solutions. Uranium, fission products, corrosion products and Thorex reagent components were studied as interfering elements in the thorium analysis. The matrix effect was also studied using the Thorex process simulated solutions. Finally, the method was applied to thorium determination in irradiated thorium solutions with satisfactory results. (author)

Measurement of trace elements in KH2PO4 crystals by x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Ryon, R.W.; Duewer, T.I.

1981-02-01

A non-destructive method is described for the quantitative measurement of impurities in KDP (KH 2 PO 4 ) crystals. Part per million concentrations of impurities can be determined with good accuracy in about one hour of instrument time. An energy dispersive x-ray spectrometer is used. Both the crystals and the solutions from which they are grown may be analyzed

Multivariate statistical approximation of the in situ gamma-ray spectrometry of the State of Zacatecas, Mexico

Energy Technology Data Exchange (ETDEWEB)

Lopez I, J. F.; Rios M, C.; Mireles G, F.; Saucedo A, S.; Davila R, I.; Pinedo, J.L., E-mail: fernandolf498@gmail.com [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98060 Zacatecas, Zac. (Mexico)

2017-09-15

The environmental radioactivity evaluation is a key point in the assessment of the environmental quality. Through this, it can be found possible radioactive contamination, locate possible Uranium and Thorium deposits and evaluate the primordial isotopes concentration due to human activities. A radioactive map of the Zacatecas State, Mexico is under construction based on in situ gamma-ray spectrometry. The present work reports the results of the multivariate statistical approximation of the measured activity data. Based on Pearson correlation, the {sup 228}Ac and {sup 208}Tl activities are statistically significant, while the {sup 214}Bi and {sup 214}Pb activities are not statistically significant. These can be due to the existence or not of secular equilibrium in the Thorium and Uranium series. (Author)

The determination, by x-ray-fluorescence spectrometry, of gold in activated charcoal

International Nuclear Information System (INIS)

Austen, C.E.

1977-01-01

A rapid method is described for the determination of gold in activated charcoal by X-ray-fluorescence spectrometry. Compensation for matrix effects is achieved by means of platinum that is added for use as an internal standard. Calibration is achieved by use of a series of synthetic standards that are made by the spiking of barren charcoal with gold and platinum. The limit of determination is about 8 p.p.m. of gold, and the relative standard deviation is 1,2 per cent at a concentration level of 2300 p.p.m

Evaluation on the stability of Hg in ABS disk CRM during measurements by wavelength dispersive X-ray fluorescence spectrometry.

Science.gov (United States)

Ohata, Masaki; Kidokoro, Toshihiro; Hioki, Akiharu

2012-01-01

The stability of Hg in an acrylonitrile-butadiene-styrene disk certified reference material (ABS disk CRM, NMIJ CRM 8116-a) during measurements by wavelength dispersion X-ray fluorescence (WD-XRF) analysis was evaluated in this study. The XRF intensities of Hg (L(α)) and Pb (L(α)) as well as the XRF intensity ratios of Hg (L(α))/Pb (L(α)) observed under different X-ray tube current conditions as well as their irradiation time were examined to evaluate the stability of Hg in the ABS disk CRM. The observed XRF intensities and the XRF intensity ratios for up to 32 h of measurements under 80 mA of X-ray tube current condition were constant, even though the surface of the ABS disk CRM was charred by the X-ray irradiation with high current for a long time. Moreover, the measurements on Hg and Pb in the charred disks by an energy dispersive XRF (ED-XRF) spectrometer showed constant XRF intensity ratios of Hg (L(α))/Pb (L(α)). From these results, Hg in the ABS disk CRM was evaluated to be sufficiently stable for XRF analysis.

Determination of mercury in seawater by total reflection x-ray fluorescence spectrometry after an electrochemical preconcentration method

International Nuclear Information System (INIS)

Ritschel, A.; Chinea Cano, E.; Wobrauschek, P.; Kuntner, C.; Durakbasa, M.N.

2000-01-01

A new combined method of electrodeposition of trace elements on metallic plates with subsequent total-reflection x-ray fluorescence spectrometry (TXRF) is proposed for the determination of trace metals in natural waters. The elements of interest are electroplated on highly polished niobium discs which are used as sample carriers for the TXRF measurement. The electrochemical preconcentration is performed in a flow cell under a controlled working electrode potential. The preconcentration step involves only very little manipulation which minimizes the risk of contamination of the sample. The method was investigated by analyzing inorganic mercury in sea water. A detection limit of 7 ngl -1 could be achieved for mercury in a 40 ml sea water sample. (author)

Mass spectrometry detection of G3m and IGHG3 alleles and follow-up of differential mother and neonate IgG3.

Directory of Open Access Journals (Sweden)

Célia Dechavanne

Full Text Available Mass spectrometry (MS analysis for detection of immunoglobulins (IG of the human IgG3 subclass is described that relies on polymorphic amino acids of the heavy gamma3 chains. IgG3 is the most polymorphic human IgG subclass with thirteen G3m allotypes located on the constant CH2 and CH3 domains of the gamma3 chain, the combination of which leads to six major G3m alleles. Amino acid changes resulting of extensive sequencing previously led to the definition of 19 IGHG3 alleles that have been correlated to the G3m alleles. As a proof of concept, MS proteotypic peptides were defined which encompass discriminatory amino acids for the identification of the G3m and IGHG3 alleles. Plasma samples originating from ten individuals either homozygous or heterozygous for different G3m alleles, and including one mother and her baby (drawn sequentially from birth to 9 months of age, were analyzed. Total IgG3 were purified using affinity chromatography and then digested by a combination of AspN and trypsin proteases, and peptides of interest were detected by mass spectrometry. The sensitivity of the method was assessed by mixing variable amounts of two plasma samples bearing distinct G3m allotypes. A label-free approach using the high-performance liquid chromatography (HPLC retention time of peptides and their MS mass analyzer peak intensity gave semi-quantitative information. Quantification was realized by selected reaction monitoring (SRM using synthetic peptides as internal standards. The possibility offered by this new methodology to detect and quantify neo-synthesized IgG in newborns will improve knowledge on the first acquisition of antibodies in infants and constitutes a promising diagnostic tool for vertically-transmitted diseases.

ICIT contribution to JET gamma-ray diagnostics enhancement

International Nuclear Information System (INIS)

Soare, S.; Curuia, M.; Zoita, V.

2010-01-01

Full text: Gamma-ray emission of tokamak plasmas is the result of the interaction of fast ions (fusion reaction products, including alpha particles, NBI ions, ICRH-accelerated ions) with main plasma impurities (e.g., carbon, beryllium). Gamma-ray diagnostics involve both gamma-ray imaging (cameras) and gamma-ray spectrometry (spectrometers). For the JET tokamak, gamma-ray diagnostics have been used to provide information on the characteristics of the fast ion population in plasmas. Two gamma-ray diagnostics enhancements project have been launched by JET and the MEdC/EURATOM Association has agreed to lead both of them with ICIT as projects leader. (authors)

Measurement of the Cosmic Ray primary spectrum with ARGO-YBJ experiment

International Nuclear Information System (INIS)

Panico, B; Iuppa, R; Di Sciascio, G

2013-01-01

The study of cosmic ray physic of 10 12 – 10 15 primary cosmic energy is one of the main goals of ARGO-YBJ experiment. The detector, located at the Yangbajing Cosmic Ray Laboratory (Tibet, 4300 m a.s.l., 606 g/cm 2 ), is an EAS array consisting of a continuous carpet of RPCs. The low energy threshold of the detector allows to study an energy region characterized by the transition from the direct to the indirect measurements. In this talk we will report on the measurement of the cosmic ray energy spectrum at different zenith angles. The phenomenology of horizontal air shower (θ > 70°) will be described and discussed.

Rigorous quantitative elemental microanalysis by scanning electron microscopy/energy dispersive x-ray spectrometry (SEM/EDS) with spectrum processing by NIST DTSA-II

Science.gov (United States)

Newbury, Dale E.; Ritchie, Nicholas W. M.

2014-09-01

Quantitative electron-excited x-ray microanalysis by scanning electron microscopy/silicon drift detector energy dispersive x-ray spectrometry (SEM/SDD-EDS) is capable of achieving high accuracy and high precision equivalent to that of the high spectral resolution wavelength dispersive x-ray spectrometer even when severe peak interference occurs. The throughput of the SDD-EDS enables high count spectra to be measured that are stable in calibration and resolution (peak shape) across the full deadtime range. With this high spectral stability, multiple linear least squares peak fitting is successful for separating overlapping peaks and spectral background. Careful specimen preparation is necessary to remove topography on unknowns and standards. The standards-based matrix correction procedure embedded in the NIST DTSA-II software engine returns quantitative results supported by a complete error budget, including estimates of the uncertainties from measurement statistics and from the physical basis of the matrix corrections. NIST DTSA-II is available free for Java-platforms at: http://www.cstl.nist.gov/div837/837.02/epq/dtsa2/index.html).

In Vitro assessment of dentin erosion after immersion in acidic beverages: surface profile analysis and energy-dispersive X-ray fluorescence spectrometry study

OpenAIRE

Caneppele, Taciana Marco Ferraz; Jeronymo, Raffaela Di Iorio; Di Nicoló, Rebeca; Araújo, Maria Amélia Máximo de; Soares, Luís Eduardo Silva

2012-01-01

The aim of this study was to investigate the effects of some acidic drinks on dentin erosion, using methods of surface profile (SP) analysis and energy-dispersive X-ray fluorescence spectrometry (EDXRF). One hundred standardized dentin slabs obtained from bovine incisor roots were used. Dentin slabs measuring 5x5 mm were ground flat, polished and half of each specimen surface was protected with nail polish. For 60 min, the dentin surfaces were immersed in 50 mL of 5 different drinks (Gatorade...

Mass spectrometry of long-lived radionuclides

International Nuclear Information System (INIS)

Becker, Johanna Sabine.

2003-01-01

The capability of determining element concentrations at the trace and ultratrace level and isotope ratios is a main feature of inorganic mass spectrometry. The precise and accurate determination of isotope ratios of long-lived natural and artificial radionuclides is required, e.g. for their environmental monitoring and health control, for studying radionuclide migration, for age dating, for determining isotope ratios of radiogenic elements in the nuclear industry, for quality assurance and determination of the burn-up of fuel material in a nuclear power plant, for reprocessing plants, nuclear material accounting and radioactive waste control. Inorganic mass spectrometry, especially inductively coupled plasma mass spectrometry (ICP-MS) as the most important inorganic mass spectrometric technique today, possesses excellent sensitivity, precision and good accuracy for isotope ratio measurements and practically no restriction with respect to the ionization potential of the element investigated--therefore, thermal ionization mass spectrometry (TIMS), which has been used as the dominant analytical technique for precise isotope ratio measurements of long-lived radionuclides for many decades, is being replaced increasingly by ICP-MS. In the last few years instrumental progress in improving figures of merit for the determination of isotope ratio measurements of long-lived radionuclides in ICP-MS has been achieved by the application of a multiple ion collector device (MC-ICP-MS) and the introduction of the collision cell interface in order to dissociate disturbing argon-based molecular ions, to reduce the kinetic energy of ions and neutralize the disturbing noble gas ions (e.g. of 129 Xe + for the determination of 129 I). The review describes the state of the art and the progress of different inorganic mass spectrometric techniques such as ICP-MS, laser ablation ICP-MS vs. TIMS, glow discharge mass spectrometry, secondary ion mass spectrometry, resonance ionization mass

Uranium enrichment measurement by X- and γ-ray spectrometry with the 'URADOS' process

International Nuclear Information System (INIS)

Morel, Jean; Etcheverry, Michel; Riazuelo, Gilles

1998-01-01

The methods used for the uranium enrichment measurement require in general prior instrument calibration with several standards. Thus, it is possible to avoid the constraints involved in calibration by considering the complex spectral region called XK α . This spectral region is sufficiently limited so that the variation of the detector efficiency response is small enough to facilitate a self-calibration. Processing this region is critical and requires taking into account 3 elemental images, one corresponding to 235 U, one to 238 U and one to the X-ray fluorescence induced in the sample by radiation above 100 keV. A process called 'URADOS' based on this principle has been developed. Six uranium oxide standards with different enrichments and infinite thicknesses were counted several times to test this process; other samples, some highly enriched, were also used. The results obtained are compared to the declared values. From these measurements, it has been possible to improve the photon emission probability values

Efficient isotope ratio analysis of uranium particles in swipe samples by total-reflection x-ray fluorescence spectrometry and secondary ion mass spectrometry

International Nuclear Information System (INIS)

Esaka, Fumitaka; Watanabe, Kazuo; Fukuyama, Hiroyasu; Onodera, Takashi; Esaka, Konomi T.; Magara, Masaaki; Sakurai, Satoshi; Usuda, Shigekazu

2004-01-01

A new particle recovery method and a sensitive screening method were developed for subsequent isotope ratio analysis of uranium particles in safeguards swipe samples. The particles in the swipe sample were recovered onto a carrier by means of vacuum suction-impact collection method. When grease coating was applied to the carrier, the recovery efficiency was improved to 48±9%, which is superior to that of conventionally-used ultrasoneration method. Prior to isotope ratio analysis with secondary ion mass spectrometry (SIMS), total reflection X-ray fluorescence spectrometry (TXRF) was applied to screen the sample for the presence of uranium particles. By the use of Si carriers in TXRF analysis, the detection limit of 22 pg was achieved for uranium. By combining these methods with SIMS, the isotope ratios of 235 U/ 238 U for individual uranium particles were efficiently determined. (author)

Low-energy X-ray and gamma spectrometry using silicon photodiodes; Espectrometria de raios X e gama de baixa energia utilizando fotodiodos de silicio

Energy Technology Data Exchange (ETDEWEB)

Silva, Iran Jose Oliveira da

2000-08-01

The use of semiconductor detectors for radiation detection has increased in recent years due to advantages they present in comparison to other types of detectors. As the working principle of commercially available photodiodes is similar to the semiconductor detector, this study was carried out to evaluate the use of Si photodiodes for low energy x-ray and gamma spectrometry. The photodiodes investigated were SFH-205, SFH-206, BPW-34 and XRA-50 which have the following characteristics: active area of 0,07 cm{sup 2} and 0,25 cm{sup 2}, thickness of the depletion ranging from 100 to 200 {mu}m and junction capacitance of 72 pF. The photodiode was polarized with a reverse bias and connected to a charge sensitive pre-amplifier, followed by a amplifier and multichannel pulse analyzer. Standard radiation source used in this experiment were {sup 241} Am, {sup 109} Cd, {sup 57} Co and {sup 133} Ba. The X-ray fluorescence of lead and silver were also measured through K- and L-lines. All the measurements were made with the photodiodes at room temperature.The results show that the responses of the photodiodes very linear by the x-ray energy and that the energy resolution in FWHM varied between 1.9 keV and 4.4 keV for peaks corresponding to 11.9 keV to 59 keV. The BPW-34 showed the best energy resolution and the lower dark current. The full-energy peak efficiency was also determined and it was observed that the peak efficiency decreases rapidly above 50 keV. The resolution and efficiency are similar to the values obtained with other semiconductor detectors, evidencing that the photodiodes used in that study can be used as a good performance detector for low energy X-ray and gamma spectrometry. (author)

High resolution gamma-ray spectrometry of culverts containing transuranic waste at the Savannah River Site

International Nuclear Information System (INIS)

Hofstetter, K.J.; Sigg, R.

1990-01-01

A number of concrete culverts used to retrievably store drummed, dry, radioactive waste at the Savannah River Site (SRS), were suspected of containing ambiguous quantities of transuranic (TRU) nuclides. These culverts were assayed in place for Pu-239 content using thermal and fast neutron counting techniques. High resolution gamma-ray spectroscopy on 17 culverts, having neutron emission rates several times higher than expected, showed characteristic gamma-ray signatures of neutron emitters other than Pu-239 (e.g., Pu-238, Pu/Be, or Am/Be neutron sources). This study confirmed the Pu-239 content of the culverts with anomalous neutron rates and established limits on the Pu-239 mass in each of the 17 suspect culverts by in-field, non-intrusive gamma-ray measurements

A convenient method for X-ray analysis in TEM that measures mass thickness and composition

Science.gov (United States)

Statham, P.; Sagar, J.; Holland, J.; Pinard, P.; Lozano-Perez, S.

2018-01-01

We consider a new approach for quantitative analysis in transmission electron microscopy (TEM) that offers the same convenience as single-standard quantitative analysis in scanning electron microscopy (SEM). Instead of a bulk standard, a thin film with known mass thickness is used as a reference. The procedure involves recording an X-ray spectrum from the reference film for each session of acquisitions on real specimens. There is no need to measure the beam current; the current only needs to be stable for the duration of the session. A new reference standard with a large (1 mm x 1 mm) area of uniform thickness of 100 nm silicon nitride is used to reveal regions of X-ray detector occlusion that would give misleading results for any X-ray method that measures thickness. Unlike previous methods, the new X-ray method does not require an accurate beam current monitor but delivers equivalent accuracy in mass thickness measurement. Quantitative compositional results are also automatically corrected for specimen self-absorption. The new method is tested using a wedge specimen of Inconel 600 that is used to calibrate the high angle angular dark field (HAADF) signal to provide a thickness reference and results are compared with electron energy-loss spectrometry (EELS) measurements. For the new X-ray method, element composition results are consistent with the expected composition for the alloy and the mass thickness measurement is shown to provide an accurate alternative to EELS for thickness determination in TEM without the uncertainty associated with mean free path estimates.

Measurements of atmospheric and gamma rays-balloon experiments at subantartic region

International Nuclear Information System (INIS)

Jayanthi, U.B.; Correa, R.V.; Blanco, F.G.

1986-01-01

The results of two stratospheric balloon experiments conducted to measure the atmospheric X and gamma rays are presented. These experiments, conducted at Comandante Ferraz base in subantarctic region, have provided the spectrum of ground radioactivity in gamma rays (0.2 to 2.9 MeV) and atmospheric X-ray spectra at different altitudes. We specifically chose to discuss the observed ceiling spectrum of X-rays in the 28 to 180KeV region observed at 7.0 g. cm -2 . We have utilized the data of other experiments with different telescope geometries, to evaluate the builup effects due to cosmic ray secondaries in atmosphere. This behaviour, previoulsy studied for atmospheric gamma rays, permitted to compare the up/down flux rations to explain the observed atmospheric X-ray spectrum. (Author) [pt

Specialised software utilities for gamma-ray spectrometry. Computer codes to IAEA-TECDOC-1275

International Nuclear Information System (INIS)

2002-03-01

A Co-ordinated Research Project (CRP) on 'Software Utilities for Gamma-Ray Spectrometry' was initiated by the International Atomic Energy Agency in 1996. In the CRP several basic applications of nuclear data handling were assayed which also dealt with the development of PC computer codes for various spectrometric purposes. This CD-ROM contains the following computer codes, produced under the CRP: ANGES, a program for the user controlled analysis of gamma-ray spectra from HPGe detectors; NUCL M AN, a program for the generation of gamma-ray libraries (using new, evaluated data) for specific applications; TRUE C OINC, a program to calculate true coincidence corrections; VOLUME, a program to calculate the full-energy peak efficiency calibration curve for homogeneous cylindrical sample geometries including self-attenuation correction; WINDIMEN, a program for the library driven analysis of gamma-ray spectra and for the quantification of radionuclide contents in the sample. RESFIT and DPPUNFOL, a set of programs for the definition of the detector resolution function and for unfolding of experimental annihilation spectra; MLMTEST, a program for the analysis of low-level NaI-spectra together with an extensive library of example reference spectra as well as a spectrum synthesizer

Crystallization and preliminary X-ray analysis of Escherichia coli RNase G

International Nuclear Information System (INIS)

Fang, Pengfei; Wang, Jing; Li, Xu; Guo, Min; Xing, Li; Cao, Xu; Zhu, Yi; Gao, Yan; Niu, Liwen; Teng, Maikun

2009-01-01

Full-length E. coli RNase G was overexpressed, purified and crystallized. Diffraction data were collected to a resolution of 3.4 Å. The homologous RNases RNase E and RNase G are widely distributed in bacteria and function in many important physiological processes, including mRNA degradation, rRNA maturation and so on. In this study, the crystallization and preliminary X-ray analysis of RNase G from Escherichia coli is described. Purified recombinant E. coli RNase G, which has 497 amino acids, was crystallized in the cubic space group F432, with unit-cell parameters a = b = c = 219.84 Å. X-ray diffraction data were collected to a resolution of 3.4 Å

The determination of the C, N, O and trace element content of Triticum aestivum by activation analysis, X-ray excitation and mass spectrometry

International Nuclear Information System (INIS)

Leonhardt, J.W.; Dahn, E.; Dietze, H.J.; Freyer, K.; Geisler, M.; Hartmann, G.; Jung, K.; Schelhorn, H.

1979-01-01

The results of determinations of the C, N, O and trace element content of grains, sprouts and leaves of Triticum aestivum by means of various methods of activation analysis, X-ray excitation and mass spectrometry are presented. The C and O contents were determined by X-ray excitation; the O, N, P and Si contents were measured by NAA with 14-MeV neutrons, and the trace elements were determined by NAA with thermal neutrons. A mass-spectrometric survey analysis confirmed the results obtained by NAA. The use of neutron-induced nuclear reactions together with autoradiography enabled a representative picture to be formed of the spatial distribution in two dimensions of 14 N in biological specimens. (author)

Quantification of 2D elemental distribution maps of intermediate-thick biological sections by low energy synchrotron μ-X-ray fluorescence spectrometry

Science.gov (United States)

Kump, P.; Vogel-Mikuš, K.

2018-05-01

Two fundamental-parameter (FP) based models for quantification of 2D elemental distribution maps of intermediate-thick biological samples by synchrotron low energy μ-X-ray fluorescence spectrometry (SR-μ-XRF) are presented and applied to the elemental analysis in experiments with monochromatic focused photon beam excitation at two low energy X-ray fluorescence beamlines—TwinMic, Elettra Sincrotrone Trieste, Italy, and ID21, ESRF, Grenoble, France. The models assume intermediate-thick biological samples composed of measured elements, the sources of the measurable spectral lines, and by the residual matrix, which affects the measured intensities through absorption. In the first model a fixed residual matrix of the sample is assumed, while in the second model the residual matrix is obtained by the iteration refinement of elemental concentrations and an adjusted residual matrix. The absorption of the incident focused beam in the biological sample at each scanned pixel position, determined from the output of a photodiode or a CCD camera, is applied as a control in the iteration procedure of quantification.

Hormesis of specific IgG antibody to rabies virus in serum of mice irradiated with low dose γ-rays

International Nuclear Information System (INIS)

Liu Qingjie; Chen Deqing

1998-01-01

Objective: To explore the effect of low dose ionizing radiation on specific antibody in mouse serum. Methods: Kunming strain male mice, weighing 18-22 g, aged 6-8 weeks, were immunized intraperitoneally with rabies vaccine after exposure to cobalt-60 γ-rays. The specific IgG antibody against rabies virus in mouse serum was measured. Results: (1) The serum levels of specific IgG in mice irradiated with 5-30 cGy γ-rays were significantly elevated in comparison with those in control mice (P<0.01), the optimum stimulating dose being 10 cGy. (2) Exposure to 10 cGy caused significant enhancement and earlier emergence of the peak level of specific IgG in serum. (3) The hormesis of specific IgG to rabies virus induced by 10 cGy γ-rays could last one week at least. Conclusion: Low dose ionizing radiation can enhance the level of specific antibody in mouse serum, and this effect can last for one week at least

Measurement of the vertical infiltration parameters and water redistribution in LRd and LEa soils by gamma-ray transmission technique

International Nuclear Information System (INIS)

Souza, A.D.B. de; Saito, H.; Appoloni, C.R.; Coimbra, M.M.; Parreira, P.S.

1991-01-01

The properties of soil water diffusivity and soil hydraulic conductivity of two horizons (0-20 cm and 20-40 cm) from Latossolo Roxo distrofico (LRd) and Latossolo Vermelho escuro (LEa) soil samples, have been measured in laboratory through the vertical infiltration and redistribution of water in soil columns. The moisture profile as a function of time for each position in the soil column were obtained with the gamma-ray transmission technique, using a sup(241)Am gamma-ray source, a Na (I) T1 scintillation detector and gamma spectrometry standard electronic. (author)

Measurement of radon concentration in water by means of {alpha}, {gamma} spectrometry. Radon concentration in ground and spring water in Hiroshima Prefecture

Energy Technology Data Exchange (ETDEWEB)

Shizuma, Kiyoshi [Hiroshima Univ. (Japan)

1997-02-01

Radon ({sup 222}Rn, T{sub 1/2}=3.8235{+-}0.0003d) is {alpha}-ray releasing nuclide, so that it can not be detected by {gamma}-ray measurement. But, the daughter nuclides {sup 214}Pb (T{sub 1/2}=26.8 min) and {sup 214}Bi (T{sub 1/2}=19.9 min) release {gamma}-ray, accordingly they are measured by Ge detector. Their radioactive equilibrium is kept in the closed vessel, because their half-lives are shorter than that of radon. We developed a measurement method of radon concentration by means of {gamma}-spectrometry. We applied this method to catch radon in the atmosphere by active carbon. The same principle can be applied to radon in water. Radon concentrations in the ground water were measured in 22 points in the Higashi-Hiroshima city and 82 points in the Hiroshima prefecture. The efficiencies of {gamma}-ray were determined. The radon concentration showed between 11 and 459 Bq/l and the average was 123 Bq/l. The high concentration of radon was distributed in the spring of granitic layer and higher concentration of radon were observed in the ground water of fault. (S.Y.)

Validation of {sup 226}Ra, {sup 228}Ra and {sup 210}Pb measurements in soil and sediment samples through high resolution gamma ray spectrometry

Energy Technology Data Exchange (ETDEWEB)

Dias, Danila Carrijo da Silva; Silva, Nivaldo Carlos da; Bonifacio, Rodrigo Leandro; Guerrero, Eder Tadeu Zenun [Comissao Nacional de Energia Nuclear (LAPOC/CNEN-MG), Pocos de Caldas, MG (Brazil). Laboratorio de Pocos de Caldas

2013-07-01

Radionuclides found in ore extraction waste materials are a great source of concern regarding public health and environmental safety. One technique to determine the concentration of substances is high resolution gamma ray spectrometry using HPGe. Validating a measurement technique is essential to warrant high levels of quality to any scientific work. The Laboratory of Pocos de Caldas of the Brazilian Commission for Nuclear Energy partakes into a Quality Management System project, seeking Accreditation under ISO/IEC 17025 through the validation of techniques of chemical and radiometric analysis of environmental samples from water, soil and sediment. The focus of the Radon Laboratory at LAPOC is validation of Ra-226, Ra-228 and Pb-210 concentration determinations in soil and sediment through a gamma spectrometer system. The stages of this validation process included sample reception and preparation, detector calibration and sample analyses. Dried samples were sealed in metallic containers and analyzed after radioactive equilibrium between Ra-226 and daughters Pb-214 and Bi-214. Gamma spectrometry was performed using CANBERRA HPGe detector and gamma spectrum software Genie 2000. The photo peaks used for Ra-226 determination were 609 keV and 1020 keV of Bi-214 and 351 keV of Pb-214. For the Ra-228 determination a photopeak of 911 keV was used from its short half-life daughter Ac-228 (T1/2 = 6.12 h). For Pb-210, the photopeak of 46.5 keV was used, which, due to the low energy, self-absorption correction was needed. Parameters such as precision, bias/accuracy, linearity, detection limit and uncertainty were evaluated for that purpose. The results have pointed to satisfying results. (author)

A study on the determination of Ca/P molar ratio in calcium-hydroxyapatite by alpha excited x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Mizumoto, Yoshihiko; Iwata, Shiro.

1979-01-01

Nondestructive powdery calcium-hydroxyapatite (HAp) target was prepared by electrodeposition method. The powdery HAp was deposited on the copper electrode plate of cathode in the electrodeposition solution such as ethyl alcohol, methyl alcohol, etc. The experiments were carried out as functions of different electrodeposition solution, ethyl alcohol concentration, distance between anode and cathode, electrodeposition time and HAp amount added in bath, and distribution of HAp on the copper electrode plate obtained from each experiment was investigated by alpha excited X-ray fluorescence analysis. Ca/P molar ratio of thin HAp target prepared with this method was determined by alpha excited X-ray fluorescence spectrometry. The nondestructive HAp targets of thickness in the range of 5 mu g/cm 2 to 10 mg/cm 2 were easily prepared with comparatively simple apparatus. The HAp on the copper electrode plate was uniform thickness over 15 x 20 mm copper plate within 5%. The Ca/P molar ratio of HAp was 1.64 +- 0.05, which agreed well with stoichiometric value of 1.67 in HAp within standard deviation. (author)

Efficient high-resolution X-ray emission spectrometry using synchrotron radiation

International Nuclear Information System (INIS)

Unterumsberger, Rainer

2015-01-01

The aim of the present work is to get access to high-resolution X-Ray Emission Spectrometry (XES) at nanoscaled materials, consisting of light elements and transition metals, by the increase of the sensitivity of a Wavelength-Dispersive Spectrometer (WDS) in the soft X-Ray range. The increase of the sensitivity was achieved by a refocusing of the incident radiation. With the increased sensitivity of the WDS, it was possible to determine the chemical species of different, nominal 100 nm thin titanium oxides. The combination of the refocusing optic and calibrated spectrometer enabled the detection and deconvolution of the L-fluorescence radiation of these nanoscaled titanium oxides. Due to the calibration of the spectrometer, a reliable determination of the transition probabilities of the titanium La- and Ll-fluorescence lines as a function of the chemical state is possible. To the best of my knowledge, the determination of the transition probabilities as a function of the chemical state in the soft X-Ray range has not been investigated yet. The quality of the refocusing was characterized using different diagnostic tools. Vertical full width at half maximum (FWHM) values of the focused beam between 10 μm to 20 μm and horizontal FWHM values between 12 μm and 25 μm could be achieved over an energy range of 180 eV to 1310 eV. Using calibrated photodiodes, it was possible to determine the absolute transmission of the used single bounce monocapillary as well as to monitor the absolute photon flux. By means of the refocusing, it was possible to increase the photon flux by a factor of 4.9 experimentally. The increase of the photon flux enables the analysis of nanoscaled materials with the used spectrometer. This could be shown based on the determination of the lower limit of detection of boron Ka and titanium La. In both cases, the lower limit of detection of 0.4 nm equivalent layer thickness was achieved (about 1.10 -7 g/cm 2 to 2.10 -7 g/cm 2 or 3.10 15 atoms/cm 2 to

A self-sufficient and general method for self-absorption correction in gamma-ray spectrometry using GEANT4

International Nuclear Information System (INIS)

Hurtado, S.; Villa, M.; Manjon, G.; Garcia-Tenorio, R.

2007-01-01

This paper presents a self-sufficient and general method for measurement of the activity of low-level gamma-emitters in voluminous samples by gamma-ray spectrometry with a coaxial germanium detector. Due to self-absorption within the sample, the full-energy peak efficiency of low-energy emitters in semiconductor gamma-spectrometers depends strongly on a number of factors including sample composition, density, sample size and gamma-ray energy. As long as those commented factors are well characterized, the influence of self-absorption in the full-energy peak efficiency of low-energy emitters can be calculated using Monte Carlo method based on GEANT4 code for each individual sample. However this task is quite tedious and time consuming. In this paper, we propose an alternative method to determine this influence for voluminous samples of unknown composition. Our method combines both transmission measurements and Monte Carlo simulations, avoiding the application of Monte Carlo full-energy peak efficiency determinations for each individual sample. To test the accuracy and precision of the proposed method, we have calculated 210 Pb activity in sediments samples from an estuary located in the vicinity of several phosphates factories with the proposed method, comparing the obtained results with the ones determined in the same samples using two alternative radiometric techniques

Investigation of prompt gamma-ray yields as a function of mass and charge of 236U fission fragments

International Nuclear Information System (INIS)

Bogdzel', A.A.; Gundorin, N.A.; Duka-Zojomi, A.; Kliman, Ya.; Krishtiak, J.

1987-01-01

New experimental results determining yields of the prompt gamma-rays from the excited states decay of fission fragments are presented. 80 gamma-transitions were observed in 51 fission fragments. The measurements were performed by Ge(Li)-spectrometry in coincidence with fast ionization chamber (10g 235 U). The beam of the resonance neutrons with energy range from 0.7 to 36 eV was used

The X-ray spectrometry Si(Li) system and it's application in quantitative analysis of rare-earth elements

International Nuclear Information System (INIS)

Barbosa, J.B.S.

1985-11-01

The basic principles involved in Si(Li) system used in X-ray spectrometry is described. It also demonstrates its application in the energy range where the resolution is better than that characteristic of conventional spectrometers. The theoretical principles underlying the interaction between the electromagnetic radiation and matter, and a review on semiconductors are presented at first. It emphasizes the fluorescence phenomenon and the process of photon detection by semiconductor crystals whose properties and characteristics allow, in the specific case of Si-crystal, the confection of detectors with large sensitivity volume useful for X-ray spectrometry. In addition, the components of the Si(Li) system are described individually, with special attention to the operating aspects, and to the parameters affecting the quality of pulse height spectrum. Finally, the spectrometer performance is experimentally evaluated though the quantitative analyses of rare-earth element oxides (La, Ce, Pr, Nd). It should be stressed that this research indicates that the X-ray emission-transmission analysis is the most adequate method under the activation conditions provided by the spectrometer, where Am 241 emissor UPSILON of 60KeV is the photon source for the fluorescence. Therefore, the experimental work was extended in order to include all the necessary treatment. (Author) [pt

Cosmic-ray contribution in measurement of environmental gamma-ray dose

International Nuclear Information System (INIS)

Nagaoka, Kazunori; Honda, Kouichirou; Miyano, Keiji

1996-01-01

Nowadays several kinds of dosimeters are being used for environmental gamma-ray monitoring. However the results measured by those instruments are not always in good agreement. It may be caused from the different characteristics of dosimeters. In particular the different responses of the instruments to cosmic-rays give significant influence on the results. Environmental radiation measurements at various altitudes on Mt. Fuji were carried out using a scintillation spectrometer with 3''φ spherical NaI(Tl), a pressurized ionization chamber (PIC), an air-equivalent ionization chamber (IC), thermoluminescence dosimeters (TLD), radiophotoluminescence glass dosimeters (RPLD) and NaI(Tl) scintillation survey meters so that the response characteristics of these instruments to cosmic-rays could be clarified. Cosmic-ray contributions for all instruments were correlated with counting rate over 3 MeV by the spectrometer. Each contribution can be estimated by measurement of the counting rate. Conversion factors (nGy/h/cpm) for IC, PIC, TLD, RPLD and NaI survey meters (TCS166 and TCS121C) were 0.33, 0.32, 0.25, 0.24, 0.06 and -0.01, respectively. Self-doses of these instruments were estimated by measurements at Nokogiriyama facilities of the Institute for Cosmic Ray Research, University of Tokyo. Self-doses for TLD and RPLD were approximately 6 nGy/h. The self dose effect should be taken into consideration in environmental dose measurements. These data are expected to be useful in estimating the cosmic-ray contribution and self-dose in the measurement of environmental gamma-ray dose. (author)

Simple procedure for nutrient analysis of coffee plant with energy dispersive X-ray fluorescence spectrometry (EDXRF)

Energy Technology Data Exchange (ETDEWEB)

Tezotto, Tiago; Favarin, Jose Laercio; Neto, Ana Paula; Azevedo, Ricardo Antunes, E-mail: tiago.tezotto@usp.br [Escola Superior de Agricultura Luiz de Queiroz (ESALQ/USP), Piracicaba, SP (Brazil); Gratao, Priscila Lupino [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP/ FCAV), Jaboticabal, SP (Brazil). Dept. de Biologia Aplicada a Agropecuaria; Mazzafera, Paulo [Universidade Estadual de Campinas (UNICAMP/IB), SP (Brazil). Dept. Biologia Vegetal

2013-07-15

Nutrient analysis is used to estimate nutrient content of crop plants to manage fertilizer application for sustained crop production. Direct solid analysis of agricultural and environmental samples by energy dispersive X-ray fluorescence spectrometry (EDXRF) was chosen as alternative technique to evaluate the simultaneous multielemental quantification of the most important essential elements in coffee (Coffea arabica L.) plants. Inductively coupled plasma atomic emission spectrometry and certified reference materials made from leaves were used to calibrate and check the trueness of EDXRF method for the determination of the concentration of several nutrients in coffee leaves and branches. Fluorescence spectrometry proved to be advantageous and presented low cost as loose powder samples could be used. Samples collected from a field experiment where coffee plants were treated with excess of Ni and Zn were used to verify the practical application of the method. Good relationships were achieved between certified values and data obtained by EDXRF, with recoveries ranging from 82 to 117 %.(author)

Application of the high-spin isomer beams to the secondary fusion reaction and the measurement of g-factor

International Nuclear Information System (INIS)

Watanabe, H.; Asahi, K.; Kishida, T.; Ueno, H.; Sato, W.; Yoshimi, A.; Kobayashi, Y.; Kameda, D.; Miyoshi, H.; Fukuchi, T.; Wakabayashi, Y.; Sasaki, T.; Kibe, M.; Hokoiwa, N.; Odahara, A.; Cederwall, B.; Lagergren, K.; Podolyak, Zs.; Ishihara, M.; Gono, Y.

2004-01-01

A technique for providing high-spin isomers as probes of the fusion reaction and the measurement of g-factor has been worked out at RIKEN. In the study of the fusion reaction 12 C( 145m Sm,xn) 157-x Er, the γ rays emitted from the fusion-evaporation residue 154 Er have been successfully observed. The nuclear g-factor of the T 1/2 = 28 ns high-spin isomer in 149 Dy has been measured with the γ-ray TDPAD method

Application of delayed X-ray spectrometry to the analysis of some rare earth elements

International Nuclear Information System (INIS)

Pillay, A.E.; Mboweni, R.C.M.

1991-01-01

The capabilities of delayed x-ray spectrometry preceded by isotope-source thermal neutron activation for the specific determination of some rare earth elements (Sm, Eu, Dy, Ho) in small powdered samples was evaluated. The feasibility study relied heavily on the low-energy sensitivity of the detector used. Detection of the delayed x-rays was achieved with a 100-mm 2 Ge detector with the ability to produce optimum photopeak-to-noise ratios. The rare earth elements were chosen on the basis of their inherent favourable nuclear properties for producing a practicable x-ray yield and on the demand for their analysis. Analytical results are presented over a range of concentrations for the elements of interest and the potential of the technique for application to their general routine analysis is discussed. Interferences from the sample matrix can be suppressed to an extent that makes the method almost independent of the matrix. This and other features make the technique a strong rival to conventional activation analysis. (author)

Radiation ray measuring device

International Nuclear Information System (INIS)

Maekawa, Tatsuyuki; Ida, Masaki.

1997-01-01

The present invention provides a chained-radiation ray monitoring system which can be applied to an actual monitoring system of a nuclear power plant or the like. Namely, this device comprises a plurality of scintillation detectors. Each of the detectors has two light take-out ports for emitting light corresponding to radiation rays irradiated from the object of the measurement to optical fibers. In addition, incident light from the optical fiber by way of one of the light take-out optical ports is transmitted to the other of the ports and sent from the other optical port to the fibers. Plurality sets of measuring systems are provided in which each of the detectors are disposed corresponding to a plurality of objects to be measured. A signal processing device is (1) connected with optical fibers of plurality sets of measuring systems in conjunction, (2) detects the optical pulses inputted from the optical fibers to identify the detector from which the optical pulses are sent and (3) measures the amount of radiation rays detected by the identified detector. As a result, the device of the present invention can form a measuring system with redundancy. (I.S.)

Conceptual design of the Radial Gamma Ray Spectrometers system for α particle and runaway electron measurements at ITER

DEFF Research Database (Denmark)

Nocente, Massimo; Tardocchi, Marco; Barnsley, Robin

2017-01-01

We here present the principles and main physics capabilities behind the design of the radial gamma ray spectrometers (RGRS) system for alpha particle and runaway electron measurements at ITER. The diagnostic benefits from recent advances in gamma-ray spectrometry for tokamak plasmas and combines...... the measurements sensitive to α particles at characteristic resonant energies and to possible anisotropies of their slowing down distribution function. An independent assessment of the neutron rate by gamma-ray emission is also feasible. In case of runaway electrons born in disruptions with a typical duration...... of 100ms, a time resolution of at least 10ms for runaway electron studies can be achieved depending on the scenario and down to a current of 40 kA by use of external gas injection. We find that the bremsstrahlung spectrum in the MeV range from confined runaways is sensitive to the electron velocity space...

Simulation of single grid-based phase-contrast x-ray imaging (g-PCXI)

Energy Technology Data Exchange (ETDEWEB)

Lim, H.W.; Lee, H.W. [Department of Radiation Convergence Engineering, iTOMO Group, Yonsei University, 1 Yonseidae-gil, Wonju, Gangwon-do 26493 (Korea, Republic of); Cho, H.S., E-mail: hscho1@yonsei.ac.kr [Department of Radiation Convergence Engineering, iTOMO Group, Yonsei University, 1 Yonseidae-gil, Wonju, Gangwon-do 26493 (Korea, Republic of); Je, U.K.; Park, C.K.; Kim, K.S.; Kim, G.A.; Park, S.Y.; Lee, D.Y.; Park, Y.O.; Woo, T.H. [Department of Radiation Convergence Engineering, iTOMO Group, Yonsei University, 1 Yonseidae-gil, Wonju, Gangwon-do 26493 (Korea, Republic of); Lee, S.H.; Chung, W.H.; Kim, J.W.; Kim, J.G. [R& D Center, JPI Healthcare Co., Ltd., Ansan 425-833 (Korea, Republic of)

2017-04-01

Single grid-based phase-contrast x-ray imaging (g-PCXI) technique, which was recently proposed by Wen et al. to retrieve absorption, scattering, and phase-gradient images from the raw image of the examined object, seems a practical method for phase-contrast imaging with great simplicity and minimal requirements on the setup alignment. In this work, we developed a useful simulation platform for g-PCXI and performed a simulation to demonstrate its viability. We also established a table-top setup for g-PCXI which consists of a focused-linear grid (200-lines/in strip density), an x-ray tube (100-μm focal spot size), and a flat-panel detector (48-μm pixel size) and performed a preliminary experiment with some samples to show the performance of the simulation platform. We successfully obtained phase-contrast x-ray images of much enhanced contrast from both the simulation and experiment and the simulated contract seemed similar to the experimental contrast, which shows the performance of the developed simulation platform. We expect that the simulation platform will be useful for designing an optimal g-PCXI system. - Highlights: • It is proposed for the single grid-based phase-contrast x-ray imaging (g-PCXI) technique. • We implemented for a numerical simulation code. • The preliminary experiment with several samples to compare is performed. • It is expected to be useful to design an optimal g-PCXI system.

Determination of As concentration in earthworm coelomic fluid extracts by total-reflection X-ray fluorescence spectrometry

Science.gov (United States)

Allegretta, Ignazio; Porfido, Carlo; Panzarino, Onofrio; Fontanella, Maria Chiara; Beone, Gian Maria; Spagnuolo, Matteo; Terzano, Roberto

2017-04-01

Earthworms are often used as sentinel organisms to study As bioavailability in polluted soils. Arsenic in earthworms is mainly sequestrated in the coelomic fluids whose As content can therefore be used to asses As bioavalability. In this work, a method for determining As concentration in coelomic fluid extracts using total-reflection X-ray fluorescence spectrometry (TXRF) is presented. For this purpose coelomic fluid extracts from earthworms living in three polluted soils and one non-polluted (control) soil have been collected and analysed. A very simple sample preparation was implemented, consisting of a dilution of the extracts with polyvinyl alcohol (PVA) using a 1:8 ratio and dropwise deposition of the sample on the reflector. A detection limit of 0.2 μg/l and quantification limit of 0.6 μg/l was obtained in the diluted samples, corresponding to 2 μg/l and 6 μg/l in the coelomic fluid extracts, respectively. This allowed to quantify As concentration in coelomic fluids extracted from earthworms living in soils polluted with As at concentrations higher than 20 mg/kg (considered as a pollution threshold for agricultural soils). The TXRF method has been validated by comparison with As concentrations in standards and by analysing the same samples by ICP-MS, after acid digestion of the sample. The low limit of detection, the proven reliability of the method and the little sample preparation make TXRF a suitable, cost-efficient and "green" technique for the analysis of As in earthworm coelomic fluid extracts for bioavailability studies.

Shaly sand evaluation using gamma ray spectrometry, applied to the North Sea Jurassic

International Nuclear Information System (INIS)

Marett, G.; Chevalier, P.; Souhaite, P.; Suau, J.

1976-01-01

In formations where radioactive minerals other than clay are present, their effects on log responses result in a reduction of the accuracy of determination of the shale fraction. The gamma ray log, which is one of the primary indicators for shaliness determination, is the most affected; other logs used in shaliness indicators are also influenced, particularly when heavy minerals are present, such as those encountered in the micaceous sandstones of the North Sea Jurassic. For comparison purposes, possible ways to correct for heavy radioactive minerals using a conventional logging suite are described. Computer processed examples illustrate the results obtained. A different approach is through an analysis of the natural gamma ray spectrum of the formation, as determined with the gamma ray spectrometry tool. Natural gamma rays originate from the radioactive isotope of potassium and the radioactive elements of the uranium and thorium series. Each of these three elements contributes its distinctive spectrum to that of the formation in proportion to its abundance. Thus, by analysis of the formation spectrum, the presence of each can be detected and its amount estimated. This makes possible quantitative corrections to the shaliness indicators. A computer program which performs the necessary computations is described, and several log examples using this technique are presented

Determination of natural radioactivity in building materials used in Tunisian dwellings by gamma ray spectrometry

International Nuclear Information System (INIS)

Hizem, N.; Fredj, A. B.; Ghedira, L.

2005-01-01

The radioisotopic content of 17 samples of natural and manufactured building materials collected in Tunisia have been analysed by using gamma spectrometry. From the measured gamma ray spectra, activity concentrations are determined for 232 Th, 226 Ra, 235 U and 40 K. The total effective dose and the activity concentration index are calculated applying the dose criteria recommended by the European Union for building materials. The results of 226 Ra, 232 Th and 40 K found in Tunisian building materials indicate that radium and thorium concentrations do not exceed 40 Bq kg -1 , but potassium concentration varies between 50 and 1215 Bq kg -1 . The total effective dose rates per person indoors are determined to be between 0.07 and 0.86 mSv y -1 . Only two materials exceed the reference level of 0.3 mSv y -1 . The activity concentration index is <1. (authors)

Standard test method for quantitative determination of americium 241 in plutonium by Gamma-Ray spectrometry

CERN Document Server

American Society for Testing and Materials. Philadelphia

1994-01-01

1.1 This test method covers the quantitative determination of americium 241 by gamma-ray spectrometry in plutonium nitrate solution samples that do not contain significant amounts of radioactive fission products or other high specific activity gamma-ray emitters. 1.2 This test method can be used to determine the americium 241 in samples of plutonium metal, oxide and other solid forms, when the solid is appropriately sampled and dissolved. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

Combined analysis of 1,3-benzodioxoles by crystalline sponge X-ray crystallography and laser desorption ionization mass spectrometry.

Science.gov (United States)

Hayashi, Yukako; Ohara, Kazuaki; Taki, Rika; Saeki, Tomomi; Yamaguchi, Kentaro

2018-03-12

The crystalline sponge (CS) method, which employs single-crystal X-ray diffraction to determine the structure of an analyte present as a liquid or an oil and having a low melting point, was used in combination with laser desorption ionization mass spectrometry (LDI-MS). 1,3-Benzodioxole derivatives were encapsulated in CS and their structures were determined by combining X-ray crystallography and MS. After the X-ray analysis, the CS was subjected to imaging mass spectrometry (IMS) with an LDI spiral-time-of-flight mass spectrometer (TOF-MS). The ion detection area matched the microscopic image of the encapsulated CS. In addition, the accumulated 1D mass spectra showed that fragmentation of the guest molecule (hereafter, guest) can be easily visualized without any interference from the fragment ions of CS except for two strong ion peaks derived from the tridentate ligand TPT (2,4,6-tris(4-pyridyl)-1,3,5-triazine) of the CS and its fragment. X-ray analysis clearly showed the presence of the guest as well as the π-π, CH-halogen, and CH-O interactions between the guest and the CS framework. However, some guests remained randomly diffused in the nanopores of CS. In addition, the detection limit was less than sub-pmol order based on the weight and density of CS determined by X-ray analysis. Spectroscopic data, such as UV-vis and NMR, also supported the encapsulation of the guest through the interaction between the guest and CS components. The results denote that the CS-LDI-MS method, which combines CS, X-ray analysis and LDI-MS, is effective for structure determination.

The measurement test of uranium in a uranium-contaminated waste by passive gamma-rays measurement method

CERN Document Server

Sukegawa, Y; Ohki, K; Suzuki, S; Yoshida, M

2002-01-01

This report is completed about the measurement test and the proofreading of passive gamma - rays measurement method for Non - destructive assay of uranium in a uranium-contaminated waste. The following are the results of the test. 1) The estimation of the amount of uranium by ionization survey meter is difficult for low intensity of gamma-rays emitted from uranium under about 50g. 2) The estimation of the amount of uranium in the waste by NaI detector is possible in case of only uranium, but the estimation from mixed spectrums with transmission source (60-cobalt) is difficult to confirm target peaks. 3) If daughter nuclides of uranium and thorium chain of uranium ore exist, measurement by NaI detector is affected by gamma-rays from the daughter nuclides seriously-As a result, the estimation of the amount of uranium is difficult. 4) The measurement of uranium in a uranium-contaminated waste by germanium detector is possible to estimate of uranium and other nuclides. 5) As to estimation of the amount of uranium...

Gamma-ray spectrometry combined with acceptable knowledge (GSAK). A technique for characterization of certain remote-handled transuranic (RH-TRU) wastes. Part 1. Methodology and techniques

International Nuclear Information System (INIS)

Hartwell, J.K.; McIlwain, M.E.

2005-01-01

Gamma-ray spectrometry combined with acceptable knowledge (GSAK) is a technique for the characterization of certain remote-handled transuranic (RH-TRU) wastes. GSAK uses gamma-ray spectrometry to quantify a portion of the fission product inventory of RH-TRU wastes. These fission product results are then coupled with calculated inventories derived from acceptable process knowledge to characterize the radionuclide content of the assayed wastes. GSAK has been evaluated and tested through several test exercises. GSAK approach is described, while test results are presented in Part II. (author)

Measurement of natural radioactivity in building materials of Namakkal, Tamil Nadu, India using gamma-ray spectrometry.

Science.gov (United States)

Ravisankar, R; Vanasundari, K; Chandrasekaran, A; Rajalakshmi, A; Suganya, M; Vijayagopal, P; Meenakshisundaram, V

2012-04-01

The natural level of radioactivity in building materials is one of the major causes of external exposure to γ-rays. The primordial radionuclides in building materials are one of the sources of radiation hazard in dwellings made of these materials. By the determination of the radioactivity level in building materials, the indoor radiological hazard to human health can be assessed. This is an important precautionary measure whenever the dose rate is found to be above the recommended limits. The aim of this work was to measure the specific activity concentration of (226)Ra, (232)Th and (40)K in commonly used building materials from Namakkal, Tamil Nadu, India, using gamma-ray spectrometer. The radiation hazard due to the total natural radioactivity in the studied building materials was estimated by different approaches. The concentrations of the natural radionuclides and the radium equivalent activity in studied samples were compared with the corresponding results of different countries. From the analysis, it is found that these materials may be safely used as construction materials and do not pose significant radiation hazards. Copyright © 2011 Elsevier Ltd. All rights reserved.

Precision measurement of radioactivity in gamma-rays spectrometry using two HPGe detectors (BEGe-6530 and GC0818-7600SL models comparison techniques: Application to the soil measurement

Directory of Open Access Journals (Sweden)

Guembou Shouop Cebastien Joel

2017-01-01

• Proved that the activity concentration determination in gamma spectrometry depended on the energy range emitted by a radionuclide. This study showed that the standard deviation measurement was less important to the result realized with BEGe-6530 HPGe model. Our findings were demonstrated that the results of the Broad Energy Germanium detector were more reliable.

Gamma-ray spectrometry combined with acceptable knowledge (GSAK). A technique for characterization of certain remote-handled transuranic (RH-TRU) wastes. Part 2. Testing and results

International Nuclear Information System (INIS)

Hartwell, J.K.; McIlwain, M.E.

2005-01-01

Gamma-ray spectrometry combined with acceptable knowledge (GSAK) is a technique for the characterization of certain remote-handled transuranic (RH-TRU) wastes. GSAK uses gamma-ray spectrometry to quantify a portion of the fission product inventory of RH-TRU wastes. These fission product results are then coupled with calculated inventories derived from acceptable process knowledge to characterize the radionuclide content of the assayed wastes. GSAK has been evaluated and tested through several test exercises. These tests and their results are described; while the former paper in this issue presents the methodology, equipment and techniques. (author)

Isotopic abundance measurements on solid nuclear-type samples by glow discharge mass spectrometry

International Nuclear Information System (INIS)

Betti, M.; Rasmussen, G.; Koch, L.

1996-01-01

A double-focusing glow discharge mass spectrometer (GDMS) installed in a glovebox for nuclear sample screening has been employed for isotopic measurements. Isotopic compositions of zirconium, silicon, lithium, boron, uranium and plutonium which are elements of nuclear concern have been determined. Interferences arising from the matrix sample and the discharge gas (Ar) for each of these elements are discussed. The GDMS results are compared with those from thermal ionization mass spectrometry (TIMS). For boron and lithium at μg/g-ng/g levels, the two methods gave results in good agreement. In samples containing uranium the isotopic composition obtained by GDMS was in agreement with those from TIMS independently of the enrichment. Attempts for the determination of plutonium isotopic composition were also made. In this case, due to the interferences of uranium at mass 238 and americium at mass 241, the GDMS raw data are complementary with those values obtained from physical non-destructive techniques. (orig.). With 2 figs., 4 tabs

Measurement of natural radioactivity in building materials of Namakkal, Tamil Nadu, India using gamma-ray spectrometry

International Nuclear Information System (INIS)

Ravisankar, R.; Vanasundari, K.; Chandrasekaran, A.; Rajalakshmi, A.; Suganya, M.; Vijayagopal, P.; Meenakshisundaram, V.

2012-01-01

The natural level of radioactivity in building materials is one of the major causes of external exposure to γ-rays. The primordial radionuclides in building materials are one of the sources of radiation hazard in dwellings made of these materials. By the determination of the radioactivity level in building materials, the indoor radiological hazard to human health can be assessed. This is an important precautionary measure whenever the dose rate is found to be above the recommended limits. The aim of this work was to measure the specific activity concentration of 226 Ra, 232 Th and 40 K in commonly used building materials from Namakkal, Tamil Nadu, India, using gamma-ray spectrometer. The radiation hazard due to the total natural radioactivity in the studied building materials was estimated by different approaches. The concentrations of the natural radionuclides and the radium equivalent activity in studied samples were compared with the corresponding results of different countries. From the analysis, it is found that these materials may be safely used as construction materials and do not pose significant radiation hazards. - Highlights: ► Most of the building materials contain natural radionuclides. ► The radioactivity level in building materials is used to assess the radiological hazards to human. ► We present the results for the measured activities and radiation hazards of building materials. ► We report that the studied building materials do not pose any significant radiation hazard.

Analysis of metal-laden water via portable X-ray fluorescence spectrometry

Science.gov (United States)

Pearson, Delaina; Weindorf, David C.; Chakraborty, Somsubhra; Li, Bin; Koch, Jaco; Van Deventer, Piet; de Wet, Jandre; Kusi, Nana Yaw

2018-06-01

A rapid method for in-situ elemental composition analysis of metal-laden water would be indispensable for studying polluted water. Current analytical lab methods to determine water quality include flame atomic absorption spectrometry (FAAS), atomic absorption spectrophotometry (AAS), electrothermal atomic absorption spectrometry (EAAS), and inductively coupled plasma (ICP) spectroscopy. However only two field methods, colorimetry and absorptiometry, exist for elemental analysis of water. Portable X-ray fluorescence (PXRF) spectrometry is an effective method for elemental analysis of soil, sediment, and other matrices. However, the accuracy of PXRF is known to be affected while scanning moisture-laden soil samples. This study sought to statistically establish PXRF's predictive ability for various elements in water at different concentrations relative to inductively coupled plasma atomic emission spectroscopy (ICP-AES). A total of 390 metal-laden water samples collected from leaching columns of mine tailings in South Africa were analyzed via PXRF and ICP-AES. The PXRF showed differential effectiveness in elemental quantification. For the collected water samples, the best relationships between ICP and PXRF elemental data were obtained for K and Cu (R2 = 0.92). However, when scanning ICP calibration solutions with elements in isolation, PXRF results indicated near perfect agreement; Ca, K, Fe, Cu and Pb produced an R2 of 0.99 while Zn and Mn produced an R2 of 1.00. The utilization of multiple PXRF (stacked) beams produced stronger correlation to ICP relative to the use of a single beam in isolation. The results of this study demonstrated the PXRF's ability to satisfactorily predict the composition of metal-laden water as reported by ICP for several elements. Additionally this study indicated the need for a "Water Mode" calibration for the PXRF and demonstrates the potential of PXRF for future study of polluted or contaminated waters.

Mapping of radiation anomalies using UAV mini-airborne gamma-ray spectrometry.

Science.gov (United States)

Šálek, Ondřej; Matolín, Milan; Gryc, Lubomír

2018-02-01

Localization of size-limited gamma-ray anomalies plays a fundamental role in uranium prospecting and environmental studies. Possibilities of a newly developed mini-airborne gamma-ray spectrometric equipment were tested on a uranium anomaly near the village of Třebsko, Czech Republic. The measurement equipment was based on a scintillation gamma-ray spectrometer specially developed for unmanned aerial vehicles (UAV) mounted on powerful hexacopter. The gamma-ray spectrometer has two 103 cm 3 BGO scintillation detectors of relatively high sensitivity. The tested anomaly, which is 80 m by 40 m in size, was investigated by ground gamma-ray spectrometric measurement in a detail rectangular measurement grid. Average uranium concentration is 25 mg/kg eU attaining 700 mg/kg eU locally. The mini-airborne measurement across the anomaly was carried out on three 100 m long parallel profiles at eight flight altitudes from 5 to 40 m above the ground. The resulting 1 s 1024 channel gamma-ray spectra, recorded in counts per second (cps), were processed to concentration units of K, U and Th, while total count (TC) was reported in cps. Increased gamma ray intensity of the anomaly was indicated by mini-airborne measurement at all profiles and altitudes, including the highest altitude of 40 m, at which the recorded intensity is close to the natural radiation background. The reported instrument is able to record data with comparable quality as standard airborne survey, due to relative sensitive detector, lower flight altitude and relatively low flight speed of 1 m/s. The presented experiment brings new experience with using unmanned semi-autonomous aerial vehicles and the latest mini-airborne radiometric instrument. The experiment has demonstrated the instrument's ability to localize size-limited uranium anomalies. Copyright © 2017 Elsevier Ltd. All rights reserved.

Assembly of positioner of automated two-dimensional scan coupled to X-ray fluorescence spectrometry; Montagem de posicionador de varredura bidimensional automatizada acoplado a espectrometria de fluorescência de raios-X

Energy Technology Data Exchange (ETDEWEB)

Silva, Leonardo Santiago Melgaço

2011-07-01

This work describes the design and assembling of a prototype automated positioner two-dimensional scanning coupled to X-ray fluorescence spectrometry. The work aims to achieve a portable and easy to use, device of broad utility in the analysis of samples by X-ray fluorescence area of expertise and research. The two-dimensional scanning of the positioner is by means of two stepper motors controlled by a microcontroller PIC 16F877A, encoder and optical sensors. The user interacts with the XY table through an interface program for the Windows operating system, which communicates with the microcontroller through the serial port. The system of Fluorescence Spectroscopy incorporated into the positioner consists of a system commercially available system from the company AMPTEK, where the primary source of excitation of the sample was a source of {sup 241}Am of 59.5 KeV emissions. Resolution and accuracy of tests were performed in the XY scanning process and reproducibility of the same kit with the fluorescence spectrometry X-ray. Qualitative tests by X-ray fluorescence spectrometry in samples were performed to demonstrate the applicability and versatility of the project. It follows that the prototype illustrates a possible adequately to portable device for X-ray spectrometry of two-dimensional. (author)

Determination of nickel in chloralkali electrolysis brines by X-ray fluorescence spectrometry on a membrane filter

International Nuclear Information System (INIS)

Andrade, L.L.; Minzl, E.

1984-01-01

X-ray fluorescence spectrometry after ammonium pyrrolidinedithiocarbamate (APDC) preconcentration is proposed for the determination of nickel in chloralkali electrolysis brines. The optimum conditions for the precipitation target tube, peak intensity, background, analysing crystal, counters and exposure time were investigated. The method was applied to chloralkali brines of evaporite salts (halite, sylvinite, carnallite and tachhydrite), sodium, potassium and magnesium salts, explored in Sergipe (Brazil), by Petrobras-Mineracao S.A.(Author) [pt

On-line interrogation of pebble bed reactor fuel using passive gamma-ray spectrometry

Science.gov (United States)

Chen, Jianwei

The Pebble Bed Reactor (PBR) is a helium-cooled, graphite-moderated high temperature nuclear power reactor. In addition to its inherently safe design, a unique feature of this reactor is its multipass fuel cycle in which graphite fuel pebbles (of varying enrichment) are randomly loaded and continuously circulated through the core until they reach their prescribed end-of-life burnup limit (˜80,000--100,000 MWD/MTU). Unlike the situation with conventional light water reactors (LWRs), depending solely on computational methods to perform in-core fuel management will be highly inaccurate. As a result, an on-line measurement approach becomes the only accurate method to assess whether a particular pebble has reached its end-of-life burnup limit. In this work, an investigation was performed to assess the feasibility of passive gamma-ray spectrometry assay as an approach for on-line interrogation of PBR fuel for the simultaneous determination of burnup and enrichment on a pebble-by-pebble basis. Due to the unavailability of irradiated or fresh pebbles, Monte Carlo simulations were used to study the gamma-ray spectra of the PBR fuel at various levels of burnup. A pebble depletion calculation was performed using the ORIGEN code, which yielded the gamma-ray source term that was introduced into the input of an MCNP simulation. The MCNP simulation assumed the use of a high-purity coaxial germanium detector. Due to the lack of one-group high temperature reactor cross sections for ORIGEN, a heterogeneous MCNP model was developed to describe a typical PBR core. Subsequently, the code MONTEBURNS was used to couple the MCNP model and ORIGEN. This approach allowed the development of the burnup-dependent, one-group spectral-averaged PBR cross sections to be used in the ORIGEN pebble depletion calculation. Based on the above studies, a relative approach for performing the measurements was established. The approach is based on using the relative activities of Np-239/I-132 in combination

Measurement of the fission yields of selected prompt and decay fission product gamma-rays of spontaneously fissioning 252Cf and 244Cm

International Nuclear Information System (INIS)

Reber, E.L.; Gehrke, R.J.; Aryaeinejad, R.; Hartwell, J.K.

2005-01-01

Gamma-ray spectrometry measurements have been made of the fission yields of selected γ -rays emitted by the spontaneously fissioning isotopes 252 Cf and 244 Cm. The measured γ-rays were selected based on their relative abundance in the spectrum and their freedom from interference or, in a few instances, ease of interference correction. From these data and the cumulative and independent yield data of England and Rider, those γ-rays that are primarily produced by radioactive decay, as opposed to direct yield, were converted into the decays per spontaneous fission expressed in percent and compared to cumulative yield values of England and Rider. For those γ-rays whose production is dominated by direct (independent) yield, the ratio of γ-rays per spontaneous fission is reported. The γ-ray yield can be compared to the independent yield values of England and Rider when 100% of the direct feeding passes through the γ-ray. In those cases where both cumulative and independent yields contribute to the observed γ-ray emission rate, a direct comparison is not possible but a method to quantify the contribution from each is proposed. (author)

Accelerator mass spectrometry for measurement of long-lived radioisotopes.

Science.gov (United States)

Elmore, D; Phillips, F M

1987-05-01

Particle accelerators, such as those built for research in nuclear physics, can also be used together with magnetic and electrostatic mass analyzers to measure rare isotopes at very low abundance ratios. All molecular ions can be eliminated when accelerated to energies of millions of electron volts. Some atomic isobars can be eliminated with the use of negative ions; others can be separated at high energies by measuring their rate of energy loss in a detector. The long-lived radioisotopes (10)Be, (14)C,(26)A1, 36Cl, and (129)1 can now be measured in small natural samples having isotopic abundances in the range 10(-12) to 10(- 5) and as few as 10(5) atoms. In the past few years, research applications of accelerator mass spectrometry have been concentrated in the earth sciences (climatology, cosmochemistry, environmental chemistry, geochronology, glaciology, hydrology, igneous petrogenesis, minerals exploration, sedimentology, and volcanology), in anthropology and archeology (radiocarbon dating), and in physics (searches for exotic particles and measurement of halflives). In addition, accelerator mass spectrometry may become an important tool for the materials and biological sciences.

Gamma-ray spectrometry applied to agricultural soil in the northwest of the State of Rio de Janeiro; Gamaespectrometria aplicada em solo agricola no noroeste do Estado do Rio de Janeiro

Energy Technology Data Exchange (ETDEWEB)

Santos, Andrea Cristina Lima dos; Nascimento, Carlos Tadeu Carvalho do [Instituto de Geociencias, Universidade de Brasilia, DF (Brazil); Menezes, Paulo de Tarso Luiz, E-mail: andrealima@unb.br, E-mail: carlostadeu@unb.br, E-mail: ptarsomenezes@pq.cnpq.br [Faculdade de Geologia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ (Brazil)

2008-04-15

The present work presents the use of gamma-ray spectrometry applied to precision agriculture in a sub-tropical area. Our dataset comprises measurements both in rock and residual soil. The soil dataset shows a reduction of 20% on U and Th and 10% on K, when compared to rock samples. This difference could be related to K supplementation associated to chemical fertilization. (author)

Research on digital airborne gamma-ray spectrometry

International Nuclear Information System (INIS)

Ge Liangquan; Lai Wanchang; Zeng Guoqiang; Fan Zhenguo; Xiong Shengqing; Ni Weizhong

2010-01-01

Airborne Gamma-ray Spectrometry (AGS) is a main supporting technique for looking for uranium deposits and other non-radioactive mineral deposit, as well as for investigating environmental radiation pollution and monitoring nuclear equipment. This paper describes the newest achievements about the AGS instrument developed by Chengdu university of Technology. Those are: 1) the probe of AGS is composed of 5 NaI(Tl) + PMT scintillation counters with 10 x 10 x 40 mm size, and a special temperature sensor, preamplifier with circuit negative feedback and high voltage with lower electronic noise have been designed. 2)A Y/U double channel digital controlled gain amplifier for adjusting the spectrum drift finely and high speed ADC and CPLD are designed to perform digitalized spectroscopy and to improve the energy resolution and pulse through output rate (more than 100k/s). 3) Two self-stabilization spectrum loops have been designed for spectrum stability: The first loop is roughly adjusted by temperature and the second loop is finely by Kalman filter. 4) The significant characters of new AGS system are: the detective gamma energy range is 0.02∼10.0 MeV, the spectrum drift is ±1 channel, the collecting period is 0.5-1 s, and 20 NaI(Tl)+PMT scintillation counters can be operated at the same time. (authors)

Gamma spectrometry of infinite 4Π geometry

International Nuclear Information System (INIS)

Nordemann, D.J.R.

1987-07-01

Owing to the weak absorption og gamma radiation by matter, gamma-ray spectrometry may be applied to samples of great volume. A very interesting case is that of the gamma-ray spectrometry applied with 4Π geometry around the detector on a sample assumed to be of infinite extension. The determination of suitable efficiencies allows this method to be quantitative. (author) [pt

International comparison of methods to test the validity of dead-time and pile-up corrections for high-precision. gamma. -ray spectrometry

Energy Technology Data Exchange (ETDEWEB)

Houtermans, H.; Schaerf, K.; Reichel, F. (International Atomic Energy Agency, Vienna (Austria)); Debertin, K. (Physikalisch-Technische Bundesanstalt, Braunschweig (Germany, F.R.))

1983-02-01

The International Atomic Energy Agency organized an international comparison of methods applied in high-precision ..gamma..-ray spectrometry for the correction of dead-time and pile-up losses. Results of this comparison are reported and discussed.

Concentration of Radon Progeny in Air by Alpha Spectrometry Measurement

International Nuclear Information System (INIS)

Acena, M. L.; Crespo, M. T.

1989-01-01

The concentration of radon progeny in air has been determined by alpha spectrometry measurement of 214 Po and 318 Po. A known volume of air was passed through a filter, then the alpha activity was directly measured on this filter. (Author) 15 refs

Measurements of total lead concentrations and of lead isotope ratios in whole blood by use of inductively coupled plasma source mass spectrometry

International Nuclear Information System (INIS)

Delves, H.T.; Campbell, M.J.

1988-01-01

Methods are described for the accurate and precise determination of total lead and its isotopic composition in whole blood using inductively coupled plasma source mass spectrometry (ICP-MS). Sensitivities of up to 3 x 10 6 counts s -1 for 208 Pb at a total lead concentration of 5 μmol l -1 (1 μg ml -1 ) enabled total blood lead levels to be measured in 4 min per sample, with a detection limit of 0.072 μmol l -1 (15 μg l -1 ). The agreement between ICP-MS and atomic absorption spectrometry (AAS) for this analysis was excellent: ICP-MS 0.996 x AAS -0.0165 μmol l -1 ; r 0.994. Isotope ratio measurements required 15 min to achieve the required accuracy and precision both of which were generally better than 0.5% for 206 Pb: 207 Pb and 208 Pb: 206 Pb isotopic lead ratios. The ICP-MS data for these ratios in ten quality control blood specimens has a mean bias relative to isotope dilution mass spectrometry of -0.412% for 206 Pb: 207 Pb ratios and of +0.055% for the 208 Pb: 206 Pb ratios. This level of accuracy and that of the total blood lead measurements is sufficient to permit application of these ICP-MS methods to environmental studies. (author)

Effects of X-ray tube parameters on thickness measure precision in X-ray profile gauge

International Nuclear Information System (INIS)

Miao Jichen; Wu Zhifang; Xing Guilai

2011-01-01

Instantaneous profile gauge technology has been widely used in metallurgy industry because it can on-line get the profile of steel strip. It has characters of high measure precision and wide measure range, but the X-ray tube parameters only can be set few different values during measurement. The relations of thickness measure precision and X-ray tube current, X-ray tube voltage were analyzed. The results show that the X-ray tube current affects the thickness measure precision and the X-ray tube voltage determines the thickness measure range. The method of estimating the X-ray current by thickness measure precision was provided in the end. This method is the base of X-ray source selection and X-ray source parameter's setting in the instantaneous profile gauge. (authors)

Measurement of structured purple soil porosity by using gamma ray transmission technique

International Nuclear Information System (INIS)

Costa, Elizabeth Cristina S. da; Rocha, Wilson Roberto Dejato da; Oliveira, Ricardo M. de; Silva, Luzeli Moreira da; Moreira, Anderson Camargo; Portezan, Otaio Portezan; Appoloni, Carlos Roberto; Coimbra, Melayne Martins

2002-01-01

The soil structure defines the particle arrangement which in turn largely determines the pore size distribution. In this work, we present the measurements of total, macro and microporosity for TRe soil with clayey texture. Soil samples were collected from a trench located at University of Londrina. The deformed and undeformed soil samples were collected from soil surface down to the depth of 0,50 m in 0,10 m intervals and separated into six aggregate size classes: 0.053; 0.125; 0.30; 0.71; 2 e 4 mm. We also prepared samples mixing different size classes, like as: (4+0.125), (2+0.125), (4+2+0.71), (4+2+0.30) e (4+0.30+0.125)mm. Measurements of particle density and aggregate bulk density using conventional method were performed to all depths. The linear soil attenuation coefficients and aggregate soil attenuation coefficients were measured with gamma-ray transmission system using an 241 Am (59,53 keV and 100 mCi) radiation source, a (2 x 2) in NaI scintillation detector, cylindric collimators (2 mm diameter to the source and 5 mm diameter to the detector) and gamma spectrometry standard electronics, connected to a multichannel. The obtained results for total, macro and microporosity are in a good agreement with the ones using the convention method, showing the applicability of the gamma-ray transmission method. (author)

Determination of fluorine concentrations using wavelength dispersive X-ray fluorescence (WDXRF) spectrometry to analyze fluoride precipitates.

Science.gov (United States)

Lee, H. A.; Lee, J.; Kwon, E.; Kim, D.; Yoon, H. O.

2015-12-01

In recent times, fluorine has been receiving increasing attention due to the possibility for chemical (HF) leakage accidents and its high toxicity to human and environment. In this respect, a novel approach for the determination of fluorine concentrations in water samples using wavelength dispersive X-ray fluorescence (WDXRF) spectrometry was investigated in this study. The main disadvantage of WDXRF technique for fluorine analysis is low analytical sensitivity for light elements with atomic number (Z) less than 15. To overcome this problem, we employed the precipitation reaction which fluoride is reacted with cation such as Al3+ and/or Ca2+ prior to WDXRF analysis because of their high analytical sensitivity. The cation was added in fluoride solutions to form precipitate (AlF3 and/or CaF2) and then the solution was filtered through Whatman filter. After drying at 60 °C for 5 min, the filter was coated with X-ray film and directly analyzed using WDXRF spectrometry. Consequently, we analyzed the cation on filter and subsequently fluorine concentration was calculated inversely based on chemical form of precipitate. This method can improve the analytical sensitivity of WDXRF technique for fluorine analysis and be applicable to various elements that can make precipitate.

Resonance ionization mass spectrometry system for measurement of environmental samples

International Nuclear Information System (INIS)

Pibida, L.; McMahon, C.A.; Noertershaeuser, W.; Bushaw, B.A.

2002-01-01

A resonance ionization mass spectrometry (RIMS) system has been developed at the National Institute of Standards and Technology (NIST) for sensitive and selective determination of radio-cesium in the environment. The overall efficiency was determined to be 4x10-7 with a combined (laser and mass spectrometer) selectivity of 108 for both 135Cs and 137Cs with respect to 133Cs. RIMS isotopic ratio measurements of 135Cs/ 137Cs were performed on a nuclear fuel burn-up sample and compared to measurements on a similar system at Pacific Northwest National Laboratory (PNNL) and to conventional thermal ionization mass spectrometry (TIMS). Results of preliminary RIMS investigations on a freshwater lake sediment sample are also discussed

Natural radioactivity in extreme south of Bahia, Brazil, using gamma-ray spectrometry

International Nuclear Information System (INIS)

Vasconcelos, Danilo C.; Oliveira, Arno H.; Silva, Mario R.S.; Penna, Rodrigo; Santos, Talita O.; Pereira, Claubia; Rocha, Zildete; Menezes, Maria Angela B.C.

2009-01-01

The concentrations activity of natural radionuclides in beach sand in extreme south of Bahia-Brazil was measured using gamma-ray spectrometry. The activity concentrations of 226 Ra, 232 Th and 40 K in beach sand ranged from 14.5 to 8,318.4, 20.5 to 18,450.0, 15.4 to 3,109.0 Bq/kg, with a mean value of 1,078.2, 2,429.6, and 417.0 Bq/kg respectively. The values of radiation hazard indexes in sands of Alcobaca, Caraiva and Cumuruxatiba are higher than the limits preconized by Beretka and Mathew. The use of these sands may be not safe in building constructions. The results show that the absorbed dose rates range from 20.4-15,116.6 nGy/h with mean value of 1762.7. The highest value of gamma dose rates among the studied beaches was found in Cumuruxatiba (15,116.6 nGy/h). The annual effective dose varied between 0.028 and 18.539 mSv/year, with a mean of 2.162 mSv/year. Values of Alcobaca, Trancoso, Caraiva and Cumuruxatiba are higher than the worldwide average for outdoor annual effective dose, 0.07 mSv/year. (author)

Radon potential mapping of the Tralee-Castleisland and Cavan areas (Ireland) based on airborne gamma-ray spectrometry and geology.

Science.gov (United States)

Appleton, J D; Doyle, E; Fenton, D; Organo, C

2011-06-01

The probability of homes in Ireland having high indoor radon concentrations is estimated on the basis of known in-house radon measurements averaged over 10 km × 10 km grid squares. The scope for using airborne gamma-ray spectrometer data for the Tralee-Castleisland area of county Kerry and county Cavan to predict the radon potential (RP) in two distinct areas of Ireland is evaluated in this study. Airborne data are compared statistically with in-house radon measurements in conjunction with geological and ground permeability data to establish linear regression models and produce radon potential maps. The best agreement between the percentage of dwellings exceeding the reference level (RL) for radon concentrations in Ireland (% > RL), estimated from indoor radon data, and modelled RP in the Tralee-Castleisland area is produced using models based on airborne gamma-ray spectrometry equivalent uranium (eU) and ground permeability data. Good agreement was obtained between the % > RL from indoor radon data and RP estimated from eU data in the Cavan area using terrain specific models. In both areas, RP maps derived from eU data are spatially more detailed than the published 10 km grid map. The results show the potential for using airborne radiometric data for producing RP maps.

Assessment of the suitability of different random number generators for Monte Carlo simulations in gamma-ray spectrometry

International Nuclear Information System (INIS)

Cornejo Diaz, N.; Vergara Gil, A.; Jurado Vargas, M.

2010-01-01

The Monte Carlo method has become a valuable numerical laboratory framework in which to simulate complex physical systems. It is based on the generation of pseudo-random number sequences by numerical algorithms called random generators. In this work we assessed the suitability of different well-known random number generators for the simulation of gamma-ray spectrometry systems during efficiency calibrations. The assessment was carried out in two stages. The generators considered (Delphi's linear congruential, mersenne twister, XorShift, multiplier with carry, universal virtual array, and non-periodic logistic map based generator) were first evaluated with different statistical empirical tests, including moments, correlations, uniformity, independence of terms and the DIEHARD battery of tests. In a second step, an application-specific test was conducted by implementing the generators in our Monte Carlo program DETEFF and comparing the results obtained with them. The calculations were performed with two different CPUs, for a typical HpGe detector and a water sample in Marinelli geometry, with gamma-rays between 59 and 1800 keV. For the Non-periodic Logistic Map based generator, dependence of the most significant bits was evident. This explains the bias, in excess of 5%, of the efficiency values obtained with this generator. The results of the application-specific assessment and the statistical performance of the other algorithms studied indicate their suitability for the Monte Carlo simulation of gamma-ray spectrometry systems for efficiency calculations.

Assessment of the suitability of different random number generators for Monte Carlo simulations in gamma-ray spectrometry.

Science.gov (United States)

Díaz, N Cornejo; Gil, A Vergara; Vargas, M Jurado

2010-03-01

The Monte Carlo method has become a valuable numerical laboratory framework in which to simulate complex physical systems. It is based on the generation of pseudo-random number sequences by numerical algorithms called random generators. In this work we assessed the suitability of different well-known random number generators for the simulation of gamma-ray spectrometry systems during efficiency calibrations. The assessment was carried out in two stages. The generators considered (Delphi's linear congruential, mersenne twister, XorShift, multiplier with carry, universal virtual array, and non-periodic logistic map based generator) were first evaluated with different statistical empirical tests, including moments, correlations, uniformity, independence of terms and the DIEHARD battery of tests. In a second step, an application-specific test was conducted by implementing the generators in our Monte Carlo program DETEFF and comparing the results obtained with them. The calculations were performed with two different CPUs, for a typical HpGe detector and a water sample in Marinelli geometry, with gamma-rays between 59 and 1800 keV. For the Non-periodic Logistic Map based generator, dependence of the most significant bits was evident. This explains the bias, in excess of 5%, of the efficiency values obtained with this generator. The results of the application-specific assessment and the statistical performance of the other algorithms studied indicate their suitability for the Monte Carlo simulation of gamma-ray spectrometry systems for efficiency calculations. Copyright 2009 Elsevier Ltd. All rights reserved.

Application of the alanine detector to gamma-ray, X-ray and fast neutron dosimetry

International Nuclear Information System (INIS)

Waligorski, M.P.R.; Hansen, J.W.; Byrski, E.

1987-01-01

A dosimeter based on alanine has been developed at the INP in Krakow and at Risoe National Laboratory. Due to its near tissue-equivalence and stability of signal, measured using ESR spectrometry at room temperature, this free-radical amino-acid dosimetric system is particularly suitable for measuring X-ray, gamma-ray and fast neutron doses in the range 10-10 5 Gy. The relative effectiveness (with respect to 60 Co γ-rays) of the alanine dosimeter to 250 kVp X-rays and to cyclotron-produced fast neutrons (mean neutron energy 5.6 MeV) is measured to be 0.76± 0.06 and 0.60±0.05, respectively. The suitability of the alanine dosimeter for intercomparison gamma-ray dosimetry is also shown. The estimated absolute difference between 60 Co dosimetry at Risoe National Laboratory and at the Centre of Oncology in Krakow is about 5%, somewhat more than the experimental uncertainty. These results are based on ESR measurements performed in Krakow on about 25% of the exposed detectors. 28 refs., 2 figs., 3 tabs. (author)

Direct dating of Tantavel man by non-destructive gamma-ray spectrometry of fossil human skull Arago XXI

International Nuclear Information System (INIS)

Yokoyama, Yuji; Nguyen, Huu-Van

1981-01-01

A new method to date prehistoric samples is proposed. Non-destructive gamma-ray spectrometry with semi-conductor detector was used in the direct determination of the activities of 238 U, 234 U, 231 Pa, 230 Th and 228 Th. An age of (400sub(-96)sup(+infinite))x10 3 years was obtained from the 230 Th/ 238 U ratio of 0.975+-0.030 [fr

Airborne Gamma-Ray Survey in Latvia 1995/96

DEFF Research Database (Denmark)

Bargholz, Kim

1998-01-01

Based on Airborne Gamma-Ray Spectrometry measurements performed with the Danish AGS equipment in 1995 and 1996 maps of the natural radioactivity have been produdced for selected areas in Latvia. The calibration of the quipment have been improved by comparisons with soil sample measurements....

Determination of lead associated with airborne particulate matter by flame atomic absorption and wave-length dispersive x-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Talebi, S.M.

1997-01-01

The lead content of airborne particulate matter was determined by flame atomic absorption spectrometry (FAAS) following digestion with a mixture of nitric acid and hydrogen peroxide and also by wave-length dispersive x-ray fluorescence (WDXRF). The extraction procedure was checked by analyzing a standard reference material of airborne particulate matter (NIST, SRM -1648). It was concluded that lead can quantitatively (98%) be extracted from airborne particulate matter by the leaching process. A five-stage sequential extraction was performed to assess the potential mobility of lead associated with airborne particulate matter. Comparison of the airborne particulate lead measured by WDXRF to that measured by FAAS showed good agreement. The WDXRF method requires no time-consuming sample preparation or use of environmentally unfriendly solvents. The technique is suggested for direct determination of lead in airborne particulate matter in air pollution studies. (author)

ESTIMATION OF MEASUREMENT UNCERTAINTY IN THE DETERMINATION OF Fe CONTENT IN POWDERED TONIC FOOD DRINK USING GRAPHITE FURNACE ATOMIC ABSORPTION SPECTROMETRY

Directory of Open Access Journals (Sweden)

Harry Budiman

2010-06-01

Full Text Available The evaluation of uncertainty measurement in the determination of Fe content in powdered tonic food drink using graphite furnace atomic absorption spectrometry was carried out. The specification of measurand, source of uncertainty, standard uncertainty, combined uncertainty and expanded uncertainty from this measurement were evaluated and accounted. The measurement result showed that the Fe content in powdered tonic food drink sample was 569.32 µg/5g, with the expanded uncertainty measurement ± 178.20 µg/5g (coverage factor, k = 2, at confidende level 95%. The calibration curve gave the major contribution to the uncertainty of the final results.   Keywords: uncertainty, powdered tonic food drink, iron (Fe, graphite furnace AAS

Interfering line in trace analysis by X-ray spectrometry: Radiative auger satellites

International Nuclear Information System (INIS)

Maeda, Kuniko; Kawai, Jun.

1994-01-01

Strong characteristic X-ray lines (e.g. Kα and Kβ) are accompanied by broad low-energy satellites caused by the radiative Auger effect (RAE). In order to prove how the RAE satellites interfere the analysis of minor elements, low-energy side spectra of Ca and Ti Kβ, and Ca-Fe Kα were measured. The obtained RAE intensities are summarized together with published experimental and theoretical data. The integrated intensities of satellites due to K → MM, K → LM and K → LL RAE relative to that of Kα are determined to be of the order of 0.01-0.1%. This warns that the neglecting of the RAE satellites will introduce a serious error in trace analysis. (author)

A broadband gamma-ray spectrometry using novel unfolding algorithms for characterization of laser wakefield-generated betatron radiation

Energy Technology Data Exchange (ETDEWEB)

Jeon, Jong Ho, E-mail: jhjeon07@ibs.re.kr; Nakajima, Kazuhisa, E-mail: naka115@dia-net.ne.jp; Pathak, Vishwa Bandhu; Cho, Myung Hoon; Yoo, Byung Ju; Shin, Kang Woo [Center for Relativistic Laser Science, Institute for Basic Science (IBS), Gwangju 500-712 (Korea, Republic of); Kim, Hyung Taek; Sung, Jae Hee; Lee, Seung Ku; Choi, Il Woo [Center for Relativistic Laser Science, Institute for Basic Science (IBS), Gwangju 500-712 (Korea, Republic of); Advanced Photonics Research Institute, GIST, Gwangju 500-712 (Korea, Republic of); Rhee, Yong Joo [Nuclear Data Center, Korea Atomic Energy Research Institute, Daejeon 305-353 (Korea, Republic of); Shin, Jung Hun; Jo, Sung Ha [Advanced Photonics Research Institute, GIST, Gwangju 500-712 (Korea, Republic of); Hojbota, Calin; Cho, Byeoung Ick; Nam, Chang Hee [Center for Relativistic Laser Science, Institute for Basic Science (IBS), Gwangju 500-712 (Korea, Republic of); Department of Physics and Photon Science, GIST, Gwangju 500-712 (Korea, Republic of)

2015-12-15

We present a high-flux, broadband gamma-ray spectrometry capable of characterizing the betatron radiation spectrum over the photon energy range from 10 keV to 20 MeV with respect to the peak photon energy, spectral bandwidth, and unique discrimination from background radiations, using a differential filtering spectrometer and the unfolding procedure based on the Monte Carlo code GEANT4. These properties are experimentally verified by measuring betatron radiation from a cm-scale laser wakefield accelerator (LWFA) driven by a 1-PW laser, using a differential filtering spectrometer consisting of a 15-filter and image plate stack. The gamma-ray spectra were derived by unfolding the photostimulated luminescence (PSL) values recorded on the image plates, using the spectrometer response matrix modeled with the Monte Carlo code GEANT4. The accuracy of unfolded betatron radiation spectra was assessed by unfolding the test PSL data simulated with GEANT4, showing an ambiguity of less than 20% and clear discrimination from the background radiation with less than 10%. The spectral analysis of betatron radiation from laser wakefield-accelerated electron beams with energies up to 3 GeV revealed radiation spectra characterized by synchrotron radiation with the critical photon energy up to 7 MeV. The gamma-ray spectrometer and unfolding method presented here facilitate an in-depth understanding of betatron radiation from LWFA process and a novel radiation source of high-quality photon beams in the MeV regime.

Energy spectrum measurement of high power and high energy(6 and 9 MeV) pulsed x-ray source for industrial use

Energy Technology Data Exchange (ETDEWEB)

Takagi, Hiroyuki [Hitachi, Ltd. Power Systems Company, Ibaraki (Japan); Murata, Isao [Graduate School of Engineering, Osaka University, Osaka (Japan)

2016-06-15

Industrial X-ray CT system is normally applied to non-destructive testing (NDT) for industrial product made from metal. Furthermore there are some special CT systems, which have an ability to inspect nuclear fuel assemblies or rocket motors, using high power and high energy (more than 6 MeV) pulsed X-ray source. In these case, pulsed X-ray are produced by the electron linear accelerator, and a huge number of photons with a wide energy spectrum are produced within a very short period. Consequently, it is difficult to measure the X-ray energy spectrum for such accelerator-based X-ray sources using simple spectrometry. Due to this difficulty, unexpected images and artifacts which lead to incorrect density information and dimensions of specimens cannot be avoided in CT images. For getting highly precise CT images, it is important to know the precise energy spectrum of emitted X-rays. In order to realize it we investigated a new approach utilizing the Bayesian estimation method combined with an attenuation curve measurement using step shaped attenuation material. This method was validated by precise measurement of energy spectrum from a 1 MeV electron accelerator. In this study, to extend the applicable X-ray energy range we tried to measure energy spectra of X-ray sources from 6 and 9 MeV linear accelerators by using the recently developed method. In this study, an attenuation curves are measured by using a step-shaped attenuation materials of aluminum and steel individually, and the each X-ray spectrum is reconstructed from the measured attenuation curve by the spectrum type Bayesian estimation method. The obtained result shows good agreement with simulated spectra, and the presently developed technique is adaptable for high energy X-ray source more than 6 MeV.

Application of gamma ray spectrometry and atomic absorption spectrometry for monitoring some radionuclides and heavy metals in sediments from the sudanese red sea coast

International Nuclear Information System (INIS)

Idris, A. M.; Eltayeb, M. A.

2004-01-01

A total of 31 surface sediment samples were collected from port-sudan harbour, sawakin harbour and the fringing reefs area that are located along the Sudanese coast of the red sea. The sampling was performed to provide good spatial coverage taking into account man's activity in port-sudan harbour and the fringing reefs area. the bulk samples were analyzed for some natural and anthropogenic radionuclides ( 226 Ra, 228 Ra, 40 K, 137 Cs) using direct gamma-ray spectrometry. Concentration of some heavy metals were determined in five fractions with grain-size of 1.000-0.500 m lm, 0.500-0.250 m lm, 0.250-0.125 m lm, 0.125-0.063 m lm and less than 0.063 m lm. The fractionation process was performed using dry sieving method. A total of 155 sub-samples (fractions) were digested by wet digestion method and analyzed for Mn, Fe, Ni, Cu, Zn, and Pb using flame atomic absorption spectrometry. Quality assurance of the obtained data was achieved through the analysis of certified reference materials. the radioactivity concentration ranges of ( 226 Ra, 228 Ra, and 40 K,) are 2.5-25.1b/kg, 2.1-13.1b q/kg,21.6- 429 Bq/kg, respectively. For ( 137 Cs)measurements, the highest value is 8.3 Bq/kg while most of samples were below the detection limits of the system. The concentration ranges of Mn, Fe, Cu, Zn, and Pb are 53.3-819 mg/kg, 1.4-51 mg/g, 8-131 mg/kg 9.5-113 mg/kg, 18.4-142 mg/kg, and 4.0-26.6 mg/kg, respectively. The granulometric normalization shows that some samples were subjected to anthropogenic activities. This finding was reinforced by results that were obtained from enrichment factor calculations and statistical multivariate analysis that is principal component analysis (Pca), also the Pca indicates that silt/clay fraction (>0.063 m lm ) is the dominant source for the emission of anthropogenic activities. From viewpoint of mineralogical composition the cluster analysis has distributed the samples into tow clusters. Dominant elements in sediments (Mn and Fe ) recorded

Experimental observation of G banding verifying X-ray workers' chromosome translocation detected by FISH

International Nuclear Information System (INIS)

Sun Yuanming; Li Jin; Wang Qin; Tang Weisheng; Wang Zhiquan

2002-01-01

Objective: FISH is the most effective way of detecting chromosome aberration and many factors affect its accuracy. G-banding is used to verify the results of early X-ray workers' chromosome translocation examined by FISH. Methods: The chromosome translocations of early X-ray workers have been analysed by FISH (fluorescence in situ hybridization) and G-banding, yields of translocation treated with statistics. Results: The chromosome aberrations frequencies by tow methods are closely related. Conclusion: FISH is a feasible way to analyse chromosome aberrations of X-ray workers and reconstruct dose

SEARCHING FOR OVERIONIZED PLASMA IN THE GAMMA-RAY-EMITTING SUPERNOVA REMNANT G349.7+0.2

Energy Technology Data Exchange (ETDEWEB)

Ergin, T.; Sezer, A. [TUBITAK Space Technologies Research Institute, ODTU Campus, 06531, Ankara (Turkey); Saha, L.; Majumdar, P. [Saha Institute of Nuclear Physics, Kolkata, West Bengal 700064 (India); Gök, F. [Akdeniz University, Faculty of Education, Department of Secondary Science and Mathematics Education, Antalya, 07058 (Turkey); Ercan, E. N., E-mail: tulun.ergin@tubitak.gov.tr [Bogazici University, Physics Department, Bebek, 34342, Istanbul (Turkey)

2015-05-10

G349.7+0.2 is a supernova remnant (SNR) expanding in a dense medium of molecular clouds and interacting with clumps of molecular material emitting gamma-rays. We analyzed the gamma-ray data of the Large Area Telescope on board the Fermi Gamma-Ray Space Telescope and detected G349.7+0.2 in the energy range of 0.2–300 GeV with a significance of ∼13σ, showing no extended morphology. Modeling of the gamma-ray spectrum revealed that the GeV gamma-ray emission dominantly originates from the decay of neutral pions, where the protons follow a broken power-law distribution with a spectral break at ∼12 GeV. To search for features of radiative recombination continua in the eastern and western regions of the remnant, we analyzed the Suzaku data of G349.7+0.2 and found no evidence for overionized plasma. In this paper, we discuss possible scenarios to explain the hadronic gamma-ray emission in G349.7+0.2 and the mixed morphology nature of this SNR.

An improved in situ method for determining depth distributions of gamma-ray emitting radionuclides

International Nuclear Information System (INIS)

Benke, R.R.; Kearfott, K.J.

2001-01-01

In situ gamma-ray spectrometry determines the quantities of radionuclides in some medium with a portable detector. The main limitation of in situ gamma-ray spectrometry lies in determining the depth distribution of radionuclides. This limitation is addressed by developing an improved in situ method for determining the depth distributions of gamma-ray emitting radionuclides in large area sources. This paper implements a unique collimator design with conventional radiation detection equipment. Cylindrically symmetric collimators were fabricated to allow only those gamma-rays emitted from a selected range of polar angles (measured off the detector axis) to be detected. Positioned with its axis normal to surface of the media, each collimator enables the detection of gamma-rays emitted from a different range of polar angles and preferential depths. Previous in situ methods require a priori knowledge of the depth distribution shape. However, the absolute method presented in this paper determines the depth distribution as a histogram and does not rely on such assumptions. Other advantages over previous in situ methods are that this method only requires a single gamma-ray emission, provides more detailed depth information, and offers a superior ability for characterizing complex depth distributions. Collimated spectrometer measurements of buried area sources demonstrated the ability of the method to yield accurate depth information. Based on the results of actual measurements, this method increases the potential of in situ gamma-ray spectrometry as an independent characterization tool in situations with unknown radionuclide depth distributions

Analysis for iodide in groundwater by x-ray fluorescence spectrometry after collection as silver iodide on activated charcoal

International Nuclear Information System (INIS)

Howe, P.T.

1980-01-01

The report describes the determination of microgram quantities of iodide in water by X-ray fluorescence spectrometry. The iodide is concentrated by precipitation as silver iodide on activated charcoal. If a 60-mL sample is available, a concentration of 0.12 mg/L can be detected. Precision (2σ) at the 1-mg/L level is +- 0.08 mg/L. (auth)

Spectrometry of X-ray beams using Cadmium and Zinc Teluride detector

International Nuclear Information System (INIS)

Becker, Paulo Henriques Bastos

1997-06-01

Determination of X-ray spectra to be utilized for medical diagnostics is a complementary process to the development of procedures to be applied to the quality control of radiodiagnostics X-ray equipment. Until some years ago, that was only possible using Germanium or Silicon detectors. Both have an excellent resolution in this energy range, but present also some restrictions as there are high costs and the necessity of operating them at temperature of liquid Nitrogen, which is not always available at the measurement's place. Room temperature detectors like Cadmium Telluride and Mercury Iodine don't have these restrictions. They, however, have a lower resolution and incomplete collection of the charges produced by their interaction with radiation. With technological advance of crystal growth in general and new techniques like cooling the crystal with a Peltier cell and rise time discrimination circuits, today Cadmium Telluride detectors show a resolution very close to that from Germanium detectors. This work relates to the routine use of Cadmium and Zinc Telluride detectors for measuring X-ray spectra in loco of diagnostic X-ray units. It characterizes the properties of a commercially available detector and offers a model for stripping the measured pulse height distribution. It was also developed a collimator to allow the direct measurement of the beam. The model developed and the constructed set-up were applied to two X-ray tubes and the achieved spectra compared with some spectra available from the literature. (author)

Factors affecting in vivo measurement precision and accuracy of 109Cd K x-ray fluorescence measurements

International Nuclear Information System (INIS)

McNeill, F.E.; Stokes, L.; Kaye, W.E.

1999-01-01

109 Cd K x-ray fluorescence (XRF) measurement systems from two research centres were used to measure tibia lead content in a population (n=530) of young adults. The group mean bone lead contents (±SEM) determined by McMaster University (n=214) and the University of Maryland (n=316) were 2.80±0.51 and 2.33±0.50 μg Pb/(g bone mineral) respectively. The mean difference of 0.47±0.71 μg Pb/(g bone mineral) was not significant. There was no evidence of a systematic difference between measurements from the two systems. Measurement uncertainties for the young adults were poorer overall than uncertainties for a population of occupationally exposed men. This was because obese subjects and women were included in the study. Regressions of precision against body mass index (BMI, defined as weight/height 2 ) determined that uncertainties increased with BMI and were poorer for women than men. Measurement uncertainties (1σ) were >8 μg Pb/(g bone mineral) for women with a BMI > 0.004 kg cm -2 . Poor-precision data affected population estimates of bone lead content; an inverse correlation was found between precision and bone lead content. A small number (0.4%) of individual measurements with poor uncertainties were inaccurate to within the precision. It is suggested that obese subjects, whose BMI > 0.004 kg cm -2 , should be excluded from 109 Cd K XRF studies, as the measurement provides limited information and may be inaccurate. (author)

Ferrous Sulphate G-Values for X Rays Generated at 20 Kv and Below

Energy Technology Data Exchange (ETDEWEB)

Redpath, A. T.; Law, J.; Greening, J. R.; Randle, K. J. [Department of Medical Physics, Royal Infirmary, University of Edinburgh, Edinburgh, Scotland (United Kingdom)

1967-03-15

Ferrous sulphate G-values for X-ray beams, generated at peak energies of 20 kV and below, are reported. The X-ray unit has a Machlett fine-focus beryllium window tube and a constant potential generator. The inherent filtration of the beam is 1 mm beryllium, 0.04 mm aluminized 'Melinex' and 10 cm of air between the tube focus and the measuring systems. The energy flux in the beam passing through a defining aperture is measured calorimetically by total absorption of the X rays in gold sheet. The calorimeter is semi-adiabatic in operation and also includes an unirradiated absorber. Measurements are taken of the temperature difference between the two absorbers. As the absorbers have approximately the same thermal characteristics, external temperature variations appear the same for each, and hence are effectively reduced. X rays enter through an 0.025-mm aluminized 'Melinex' window. Thermal insulation of the absorbers from the window, and from each other, is obtained by aluminized 'Melinex' radiation shields and polytetrafluoroethylene (PTFE) rods. Fine nylon thread is used to suspend the absorbers from the PTFE rods. The assembly is enclosed in a vacuum flask, which is itself evacuated to a pressure of 10{sup -6} mm Hg. Thermal damping is improved by placing this vacuum flask in a larger vacuum flask filled with granular vermiculite. Temperature changes are detected by thermistors which constitute two arms of an A-C Wheatstone bridge. The out-of-balance voltage is amplified and displayed on a recorder. An electrical heating coil is used for calibration. Background drift rates less than 10{sup -5} degC/min are obtainable. FeSO{sub 4} irradiations are performed in polythene vessels with 0.04-mm aluminized 'Melinex' windows. The size of vessel which, when filled with FeSO{sub 4} will totally absorb the incident radiation, is obtained by direct experiment, with a calculated correction for back-scatter from the incident surface. The production of Fe{sup 3+} is measured by

DETERMINATION OF MINERAL COMPOSITION OF ORGANIC AND CONVENTIONAL BEVERAGES BY DISPERSIVE ENERGY X-RAY FLUORESCENCE SPECTROMETRY

Directory of Open Access Journals (Sweden)

L. CONSOLI

2012-11-01

Full Text Available Fruits are natural sources of minerals whose ingestion is recommended in a balanced diet. The increasing consumption of fruit-based beverages demands the development of rapid methods to evaluate their quality parameters. X-ray fluorescence spectrometry is an analytical-nuclear technique that is gaining space in the environmental and geological fields, and has been explored modestly in the food field. The main objective of this work was to develop a methodology to determine the mineral content of fruit-based beverages by applying this technique. Beverages manufactured from organic and conventional fruit varieties were evaluated, aiming to compare their nutritional value. The research was divided into three steps: in the first step, a direct measurement of the samples was made, that is, without prior preparation; in the second, standard curves were prepared with the elements of calcium and potassium, based on the category of ‘fine samples’. Lastly, these curves were used to determine concentrations of calcium and potassium in the samples of juices and pulps prepared as ‘fine samples’. The fine sample measurements showed results more exact compared to that obtained from the direct measurements. From the data evaluated, it was not possible to attribute better nutritional quality to either the organic or conventional samples.

Cortisol production rates measured by liquid chromatography/mass spectrometry

International Nuclear Information System (INIS)

Esteban, N.V.; Yergey, A.L.

1990-01-01

Cortisol production rates (FPRs) in physiologic and pathologic states in humans have been investigated over the past 30 years. However, there has been conflicting evidence concerning the validity of the currently accepted value of FPRs in humans (12 to 15 mg/m2/d) as determined by radiotracer methodology. The present study reviews previous methods proposed for the measurement of FPRs in humans and discusses the applications of the first method for the direct determination of 24-hour plasma FPRs during continuous administration of a stable isotope, using a thermospray high-pressure liquid chromatography-mass spectrometry technique. The technique is fast, sensitive, and, unlike gas chromatography-mass spectrometry methods, does not require derivatization, allowing on-line detection and quantification of plasma cortisol after a simple extraction procedure. The results of determination of plasma FPRs by stable tracer/mass spectrometry are directly in units of mass/time and, unlike radiotracer methods, are independent of any determination of volume of distribution or cortisol concentration. Our methodology offers distinct advantages over radiotracer techniques in simplicity and reliability since only single measurements of isotope ratios are required. The technique was validated in adrenalectomized patients. Circadian variations in daily FRPs were observed in normal volunteers, and, to date, results suggest a lower FRP in normal children and adults than previously believed. 88 references

Major constituent quantitative determination in uranium alloys by coupled plasma atomic emission spectrometry and X ray fluorescence wavelength dispersive spectrometry

International Nuclear Information System (INIS)

Oliveira, Luis Claudio de; Silva, Adriana Mascarenhas Martins da; Gomide, Ricardo Goncalves; Silva, Ieda de Souza

2013-01-01

A wavelength-dispersive X-ray fluorescence (WD-XRF) spectrometric method for determination of major constituents elements (Zr, Nb, Mo) in Uranium/Zirconium/Niobium and Uranium/Molybdenum alloy samples were developed. The methods use samples taken in the form of chips that were dissolved in hot nitric acid and precipitate particles melted with lithium tetraborate and dissolved in hot nitric acid and finally analyzed as a solution. Studies on the determination by inductively coupled plasma optic emission spectrometry (ICP OES) using matched matrix in calibration curve were developed. The same samples solution were analyzed in both methods. The limits of detection (LOD), linearity of the calibrations curves, recovery study, accuracy and precision of the both techniques were carried out. The results were compared. (author)

European coordination of environmental airborne gamma ray spectrometry. Final report 1999

International Nuclear Information System (INIS)

Sanderson, D.C.; McLeod, J.J.

1999-04-01

This Concerted Action was funded under the EURATOM Nuclear Fission Safety Programme of the Fourth Framework Programme, and was initiated to address transnational issues relating to environmental airborne gamma ray spectrometry (AGS). Significant development of AGS systems and teams has taken place within Europe during the period following the Chernobyl accident. The technique is increasingly recognised as particularly relevant to emergency response. It is also uniquely capable of acquiring data on anthropogenic and natural radionuclides on regional, national and international scales, for reference purposes, ecological studies and epidemiological research. Prior to this EU programme the methodologies and systems used by European AGS teams had undergone rapid and largely uncoordinated development. This raised questions about comparability of systems, applications, and data between teams, duplication of research, the scope for transnational cooperation and standardisation, and future research and development needs in the field. This project, which brought together ten AGS teams from across Europe, was formed to address these issues. The work was conducted in three stages and has largely succeeded in its objectives. An active communication network was developed for collaboration and exchange of information, and to start the process of harmonisation of the different methodologies used by individual AGS teams. Two formal partners' meetings were organised, the first aimed at defining the EU capability in AGS, the second, in the form of an international symposium (RADMAGS), was aimed at reviewing developments on future research needs and the scope for standardisation. This report gives full details of the project and its deliverables together with discussion of the further needs in support of transnational harmonisation of this topic. The European Capability for AGS was defined at an early stage of the project, and monitored throughout. An EU Bibliography on AGS

Performance of gamma spectrometry counting system

International Nuclear Information System (INIS)

Yii Mei Wo; Maziah Mahmud

2007-01-01

Gamma spectrometry counting system widely used as tool to measure qualitative and quantitative gamma-ray emitters in a sample. Container size, sample to detector distance, sample volume are well known factors that affecting the quality of measurement. However, factor such as the age of the system was not been reported. Therefore, the objective of this study is to find out how the age factor affecting the quality of the measurement. From this study, it is found that when the age of the system increased, the system tends to have higher lower limit of detection and poorer linearity showing that age factor do affecting the quality of measurement. (Author)

Simulation of the isotopic ratio determination of plutonium by Ge(Li) gamma-ray spectrometry

International Nuclear Information System (INIS)

Baba, Hiroshi; Yagi, Hideyuki

1979-09-01

A simulation program ''SIMPUG'' was developed for assessing feasibility of the isotopic ratio determination of plutonium by Ge(Li) γ-ray spectrometry. The program consists of (1) construction of the spectrum profiles for eight peak groupings of interest with a given set of isotopic compositions and by the use of the known nuclear data for emitting γ rays and (2) determination of the intensity of each participating nuclide following a presently developed algorithm of spectrum unfolding. Effects of various factors on the reliability of the results were examined with the simulation program. Accuracy of the results was found to be little affected by the change of the detector resolution if the spectrum was taken with sufficient expansion. Counting statistics was concluded to be the most essential factor for the precision of the results, while the aging effect was not found significant. Contamination of fission products beyond a certain level brought about fatal errors in the determined values, particularly in the case of minor components. (author)

Clinical review: improving the measurement of serum thyroglobulin with mass spectrometry.

Science.gov (United States)

Hoofnagle, Andrew N; Roth, Mara Y

2013-04-01

Serum thyroglobulin (Tg) measurements are central to the management of patients treated for differentiated thyroid carcinoma. For decades, Tg measurements have relied on methods that are subject to interference by commonly found substances in human serum and plasma, such as Tg autoantibodies. As a result, many patients need additional imaging studies to rule out cancer persistence or recurrence that could be avoided with more sensitive and specific testing methods. The aims of this review are to: 1) briefly review the interferences common to Tg immunoassays; 2) introduce readers to liquid chromatography-tandem mass spectrometry as a method for quantifying proteins in human serum/plasma; and 3) discuss the potential benefits and limitations of the method in the quantification of serum Tg. Mass spectrometric methods have traditionally lacked the sensitivity, robustness, and throughput to be useful clinical assays. These methods failed to meet the necessary clinical benchmarks due to the nature of the mass spectrometry workflow and instrumentation. Over the past few years, there have been major advances in reagents, automation, and instrumentation for the quantification of proteins using mass spectrometry. More recently, methods using mass spectrometry to detect and quantify Tg have been developed and are of sufficient quality to be used in the management of patients. Novel serum Tg assays that use mass spectrometry may avoid the issue of autoantibody interference and other problems with currently available immunoassays for Tg. Prospective studies are needed to fully understand the potential benefits of novel Tg assays to patients and care providers.

Neutron activation analysis of ultrabasis rock by Ge(Li) γ-ray spectrometry and group separation

International Nuclear Information System (INIS)

Chen Baoguan; Yuan Ling; Fang Chanmeng

1986-01-01

The analytical procedure for determination of 21 elements in two ultrabasis rock samples with Ge(Li) gamma-ray spectrometry and group separation was described. 8 elements including Cr, Fe, Co, Sc, Mn, Na, Cl and Br have been directly determined by INAA. 13 elements including La, Ce, Nd, Sm, Gd, Eu, Tb, Ho, Tm, Yb, Lu, Zn and Cs have been determined by radiochemical separation. The samples of international standard AGV-1 (Andesite) have also been analyzed. The agreement of the results with the values proposed by F.J.Flanagan is satisfactory

A New Method for Processing Airborne Gamma Ray Spectrometry Data for Mapping Low Level Contaminations

DEFF Research Database (Denmark)

Aage, Helle Karina; Korsbech, Uffe C C; Bargholz, Kim

1999-01-01

A new technique for processing airborne gamma ray spectrometry data has been developed. It is based on the noise adjusted singular value decomposition method introduced by Hovgaard in 1997. The new technique opens for mapping of very low contamination levels. It is tested with data from Latvia...... where the remaining contamination from the 1986 Chernobyl accident together with fallout from the atmospheric nuclear weapon tests includes Cs-137 at levels often well below 1 kBq/m(2) equivalent surface contamination. The limiting factors for obtaining reliable results are radon in the air, spectrum...

The analysis, by a fusion procedure and X-ray-fluorescence spectrometry, of silicates and slags

International Nuclear Information System (INIS)

Jacobs, J.J.; Balaes, A.M.E.

1980-01-01

A glass-disc fusion method is described for the analysis, by X-ray-fluorescence spectrometry, of slags and silicate materials. The data are corrected for detector dead time and short-term instrumental drift. Corrections are made for matrix variations by use of the Lachange-Traill mathematical model, and the results are processed on a mini-computer, an iterative procedure being used in the solving of the simultaneous equations. As the alpha-correction coefficients of the Lachange-Traill model are not truly constant, a modified version of the model is proposed [af

Study of the matrix specific mass discrimination effects during inductively coupled plasma mass spectrometry isotope ratio measurements

International Nuclear Information System (INIS)

Vassileva, E.; Quetel, Ch.R.

2004-01-01

Sample matrix related effects on mass discrimination during inductively coupled plasma mass spectrometry (ICP-MS) isotope ratio measurements have only been rarely reported. However, they can lead to errors larger than the uncertainty claimed on the ratio results when not properly taken into account or corrected for. These matrix specific affects were experienced during an Isotope Dilution Mass Spectrometry (IDMS) campaign we carried out for the certification of the Cd amount content in some food digest samples (7% acidity and salts content around 450μg g -1 ). Dilution was not possible for Cd only present at the low ng g -1 level. Up to 1% difference was observed on Cd isotope ratio results between measurements performed directly or after matrix separation. This was a significant difference considering that less than 1.5% relative combined uncertainty was eventually estimated for these IDMS measurements. Similar results could be obtained either way after the implementation of necessary corrections. The direct measurement approach associated to a correction for mass discrimination effects using the food digest sample itself (and the IUPAC table values as reference for the natural Cd isotopic composition) was preferred as it was the easiest. Consequently, the impact of matrix effects on mass discrimination during isotope ratio measurements with two types of ICP- MS (quadrupole and magnetic sector instruments) was studied for 4 elements (Li, Cu, Cd and Tl). Samples of varying salinity (up to 0.25%) and acidity (up to 7%) characteristics were prepared using isotopic certified reference materials of these elements. The long term and short-term stability, respectively reproducibility and repeatability, of the results, as well as the evolution of the difference to certified ratio values were monitored. As expected the 13 investigated isotopic ratios were all sensitive to variations in salt and acid concentrations. Our experiments also showed that simultaneous variation

Application of neutron activation techniques and x-ray energy dispersion spectrometry, in analysis of metallic traces adsorbed by chelex-100 resin; Ativacao das tecnicas de ativacao neutronica e espectrometria por dispersao de onda e de energia de raios X, na analise de tracos metalicos adsorvidos pela resina chelex-100

Energy Technology Data Exchange (ETDEWEB)

Fernandes, Jair C.; Amaral, Angela M.; Magalhaes, Jesus C.; Pereira, Jose S.J.; Silva, Juliana B. da; Auler, Lucia M.L.A. [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Belo Horizonte, MG (Brazil)]. E-mail: jcf@urano.cdtn.br

2000-07-01

In this work, the authors have investigated optimal conditions of adsorption for several ion metallic groups (cations of heavy metals and transition metals, oxyanions metallics and metalloids and cations of rare earths), as traces (ppb), withdrawn and in mixture of groups, by chelex-100 resin. The experiments have been developed by bath techniques in ammonium acetate tamponade solution 40 mM pH 5,52 content 0,5 g of chelex-100 resin. After magnetic agitation for two hours, resins were dried and submitted to X-ray energy dispersion spectrometry, x-ray fluorescence spectrometry and neutron activation analysis. The results have demonstrated that chelex-100 resin adsorb quantitatively transition element groups and rare earth groups in two cases (withdrawn and simultaneously adsorption)

Measurement of non-invasive X-ray measuring instruments

International Nuclear Information System (INIS)

Abe, Shinji

2013-01-01

Described are the history, measuring system, characteristics and present state of the instruments in the title (NXMI). NXMI, non-invasive to the inner circuit of X-ray generator, is now essential for the quality control of generator with reference to definitions by International Electrotechnical Commission (IEC) and Japan Industrial Standards (JIS). Non-invasive measurement of the generator's tube voltage in 1944 is the first report where the absorption difference of Cu plates with different thickness is used. At present, NXMI, being compact, can measure multiple properties of X-ray generated, such as the tube voltage (TV), current (TC), imaging time, dose/dose rate, total filtration, half value layer, and TV/output waveform. TV is measurable by the penetration difference of X-rays through Cu filters of different thickness, which is a linear function of TV; TC, with the clamp-type ammeter placed at the generator high voltage cable; and the dose, with the semiconductor detector. Characteristics can be evaluable within the upper trigger level of the detector (radiation time, dose measured here), in which measured are the irradiation (imaging) time, delay time, and TV (within the window width). Authors' practical quality control of the generator is conducted through calibration for which data are obtained by invasive (direct) precise measurement of TV, TC, imaging time and dose with reference to JIS. Periodical calibration and consequent quality control of NXMI are essential for the maintenance of precision of the generator. (T.T.)

Radon fixation for determination of 224Ra, 226Ra and 228Ra via gamma-ray spectrometry

International Nuclear Information System (INIS)

Herranz, M.; Idoeta, R.; Abelairas, A.; Legarda, F.

2006-01-01

The aim of this work is the improvement of the procedure for the determination of radium isotopes activities in water, which is done through radiochemical separation and subsequent gamma-ray spectrometry. In addition, radon gas retention is studied using different activated carbon materials. The results of the IAEA Proficiency test: 'Determination of radium and uranium radionuclides in water' of December 2002 [IAEA, 2003. Analytical quality control services: determination of radium and uranium radionuclides in water. Preliminary Report, Seibersdorf] are considered for this work

Characterization of some modern scintillators recommended for use on large fusion facilities in γ-ray spectroscopy and tomographic measurements of γ-emission profiles

Directory of Open Access Journals (Sweden)

Sibczynski Pawel

2017-09-01

Full Text Available LaBr3:Ce,CeBr3 and GAGG:Ce scintillators were investigated and the determined characteristics were compared with those obtained for the well-known and widely used CsI:Tl and NaI:Tl crystals. All the detectors were of the same size of 10 × 10 × 5 mm3. The aim of this test study was to single out scintillation detectors most suitable for γ-ray spectrometry and γ-ray emission radial profile measurements in high-temperature plasma experiments. Decay time, energy resolution, non-proportionality and full energy peak detection efficiency ere measured for γ-ray energies up to 1770 keV. Due to their good energy resolution, short decay time and high detection efficiency for MeV gamma rays, LaBr3:Ce and CeBr3 scintillators are proposed as the best candidates for use especially under conditions of high count rates, which are expected in the forthcoming DT experiments.

Scanning electron microscopy-energy dispersive X-ray spectrometry (SEM-EDX) and aerosol time-of-flight mass spectrometry (ATOFMS) single particle analysis of metallurgy plant emissions

International Nuclear Information System (INIS)

Arndt, J.; Deboudt, K.; Anderson, A.; Blondel, A.; Eliet, S.; Flament, P.; Fourmentin, M.; Healy, R.M.; Savary, V.; Setyan, A.; Wenger, J.C.

2016-01-01

The chemical composition of single particles deposited on industrial filters located in three different chimneys of an iron-manganese (Fe–Mn) alloy manufacturing plant have been compared using aerosol time-of-flight mass spectrometry (ATOFMS) and scanning electron microscopy–energy dispersive X-ray spectrometry (SEM-EDX). Very similar types of particles were observed using both analytical techniques. Calcium-containing particles dominated in the firing area of the sintering unit, Mn and/or Al-bearing particles were observed at the cooling area of the sintering unit, while Mn-containing particles were dominant at the smelting unit. SEM-EDX analysis of particles collected downstream of the industrial filters showed that the composition of the particles emitted from the chimneys is very similar to those collected on the filters. ATOFMS analysis of ore samples was also performed to identify particulate emissions that could be generated by wind erosion and manual activities. Specific particle types have been identified for each emission source (chimneys and ore piles) and can be used as tracers for source apportionment of ambient PM measured in the vicinity of the industrial site. - Highlights: • Similar composition for emitted particles as those collected on the chimney filters. • Emitted particles dominated by Ca-, Mn and/or Al-containing particles. • Identification of specific particle types emitted by the different process units. - The particles emitted by metallurgy activities are fully described by ATOFMS and SEM-EDX, enabling the identification of specific particle types from the different units of the process.

A rapid analysis of {sup 226}Ra in raw materials and by-products using gamma-ray spectrometry

Energy Technology Data Exchange (ETDEWEB)

Lim, Chung Sup; Chung, Kun Ho; Kim, Chang Jong; Ji, Young Yong [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2017-03-15

A gamma-ray peak of {sup 226}Ra (186.2 keV) overlaps with one of {sup 235}U (185.7 keV) in a gamma-ray spectrometry system. Though reference peaks of {sup 235}U can be used to correct the peak interference of {sup 235}U in the analysis of {sup 226}Ra, this requires a complicated calculation process and a high limit of quantitation. On the other hand, evaluating {sup 226}Ra using the correction constant in the overlapped peak can make a rapid measurement of {sup 226}Ra without the complicated calculation process as well as overcome the disadvantage in the indirect measurement of {sup 214}Bi, which means the confinement of {sup 222}Rn gas in a sample container and a time period to recover the secular equilibrium. About 93 samples with 6 species for raw-materials and by-products were prepared to evaluate the activity of {sup 226}Ra using the correction constant. The results were compared with the activity of {sup 214}Bi, which means the indirect measurement of {sup 226}Ra, to validate the method of the direct measurement of {sup 226}Ra using the correction constant. The difference between the direct and indirect measurement of {sup 226}Ra was generally below about ± 20%. However, in the case of the phospho gypsum, a large error of about 50% was found in the comparison results, which indicates the disequilibrium between {sup 238}U and {sup 226}Ra in the materials. Application results of the contribution ratio of {sup 226}Ra were below about ± 10% . The direct measurement of {sup 226}Ra using the correction constant can be an effective method for its rapid measurement of raw materials and by-products because the activity of {sup 226}Ra can be produced with a simple calculation without the consideration of the integrity of a sample container and the time period to recover the secular equilibrium.

Laboratory calibrations of airborne gamma-ray spectrometers. Measurements and discussions of important parameters

International Nuclear Information System (INIS)

Korsbech, U.

1994-02-01

This report is the fourth of reports from The Department of Electrophysics covering measurement and interpretation of airborne gamma-spectrometry measurements. It describes different topics concerning the construction of a suitable calibration setup in the laboratory. The goal is to build a simple and cheap laboratory setup that can produce most of the gamma-ray data needed for an interpretation of spectra measured 50 to 120 m above ground level. A simple calibration setup has been build and tested. It may produce gamma-ray spectra similar to those measured in the air - from surface contamination with artificial nuclides and from 'bulk' natural radioactivity. It is possible to investigate the influence of the air above an aircraft carrying the detector (skyshine: scattering of gamma photons in the air above the detector). In order to reduce the influence of non-detected pile-up the count rates are kept low without reaching levels where the background spectra (to be subtracted) would cause unacceptable counting statistical fluctuations. Sources selected for the calibrations are heavy minerals sand (with thorium and uranium), potassium nitrate (with 40 K). These sources are 'bulk sources' of natural radioactivity. Cesium-137 has been selected as the basic artifical surface contamination nuclide. The report also discusses methods for comparing two spectra a priori assumed equal. Finally the properties of some materials that could be used as 'air-substitutes' in the calibration setup have been tested with respect to stability against moisture sorption. (au)

Gamma-ray scanning of neutron activated geological sediments for studying elemental profile distributions

International Nuclear Information System (INIS)

Ellinger, M.; Janghorbani, M.; Starke, K.

1976-01-01

Gamma-ray scanning for application to elemental profile studies of geological samples was studied with a neutron activated Baltic Shield sediment. Profile distribution of seven elements were measured. The capabilities and limitations of gamma-ray scanning are discussed by comparing the results with profiles obtained after the mechanical subdivision of the sample and the activation of the appropriately sized separates. With respect to the merits and limitations of scanning gamma-ray spectrometry applied to activated complex matrices the following conclusions were drawn. Qualitatively, the scanning method yields the same information as the much more laborious method of mechanical sudbisubdivision. Quantitatively, it is significantly less accurate. The scanning method has the significant advantage of allowing preservation of the sample. This could be important for such speciments as lunar and archeological materials. The method reduces sample preparation time and the possibility of sample contamination. (T.G.)

Design and construction of the gamma ray transmission tomographer g-TAC-02

International Nuclear Information System (INIS)

Pavon Hernandez, Noriel; Ravelo Sanchez, Alberto; Idel, Pedro; Macias Perez, Rafael; Garcia Trapaga, Cesar; Campos Montenegro, Augusto

2000-01-01

An equipment for gamma ray transmission tomographer was designed and constructed in the Higher Institute of Nuclear Sciences and Technology. It was the g-TAC-01, based on a nuclear instrumentation, a mechanic instrumentation, and the control of the system from a personal computer. This first version permitted to obtain the know how of the technology of construction of equipment for tomography. The present work describes the second version of the gamma ray transmission tomographer: the g-TAC-02, with very important upgrading in the control session. Now the control system is a microcontroller based, electronic control system, designed to work in multiples forms: manual, automatic and with the computer

X-ray imaging and spectroscopic measurements of implosions

International Nuclear Information System (INIS)

Hammel, B.A.; Ress, D.R.; Keane, C.J.; Kilkenny, J.D.; Landen, O.L.; Bell, P.; Pasha, R.; Wallace, R.J.; Bradley, D.K.

1992-01-01

Time-resolved x-ray measurements are essential in the investigation of laser-driven inertial confinement fusion, where neutron and x-ray emission are the only observable signatures of the compressed core conditions. High-speed detectors, available for x-ray measurement, provide a means of measuring the rapidly evolving conditions in imploding capsules on picosecond time scales. We address a wide range of issues in our indirectly driven implosion experiments on Nova, with a large variety of x-ray measurement techniques. Critical issues include symmetry of the compressed core, fuel density and temperature and hydrodynamic mix at the pusher/fuel interface

Response Time Measurements of the NIF DANTE XRD-31 X-Ray Diodes (Pre-print)

International Nuclear Information System (INIS)

Pellinen, Don; Griffin, Michael

2009-01-01

The XRD-31 is a fast, windowless X-ray vacuum photodiode developed by EG and G. It is currently the primary fast X-ray detector used to diagnose the X-rays on NIF and OMEGA on the multichannel DANTE spectrometer. The XRD-31 has a dynamic range of less than 1e-12 amps to more than 10 amps. A technique is described to measure the impulse response of the diodes to a 150 fs pulse of 200 nm laser light and a method to calculate the 'risetime' for a square pulse and compare it with the computed electron transit time from the photocathode to the anode. Measured response time for 5 XRD-31s assembled in early 2004 was 149.7 ps +-2.75 ps

Crystallization and preliminary X-ray analysis of Chandipura virus glycoprotein G

International Nuclear Information System (INIS)

Baquero, Eduard; Buonocore, Linda; Rose, John K.; Bressanelli, Stéphane; Gaudin, Yves; Albertini, Aurélie A.

2012-01-01

Chandipura virus glycoprotein ectodomain (Gth) was purified and crystallized at pH 7.5. X-ray diffraction data set was collected to a resolution of 3.1 Å. Fusion in members of the Rhabdoviridae virus family is mediated by the G glycoprotein. At low pH, the G glycoprotein catalyzes fusion between viral and endosomal membranes by undergoing a major conformational change from a pre-fusion trimer to a post-fusion trimer. The structure of the G glycoprotein from vesicular stomatitis virus (VSV G), the prototype of Vesiculovirus, has recently been solved in its trimeric pre-fusion and post-fusion conformations; however, little is known about the structural details of the transition. In this work, a soluble form of the ectodomain of Chandipura virus G glycoprotein (CHAV G th ) was purified using limited proteolysis of purified virus; this soluble ectodomain was also crystallized. This protein shares 41% amino-acid identity with VSV G and thus its structure could provide further clues about the structural transition of rhabdoviral glycoproteins induced by low pH. Crystals of CHAV G th obtained at pH 7.5 diffracted X-rays to 3.1 Å resolution. These crystals belonged to the orthorhombic space group P2 1 2 1 2, with unit-cell parameters a = 150.3, b = 228.2, c = 78.8 Å. Preliminary analysis of the data based on the space group and the self-rotation function indicated that there was no trimeric association of the protomers. This unusual oligomeric status could result from the presence of fusion intermediates in the crystal

Radioactive characterization of samples in various geometry by gamma ray spectrometry

International Nuclear Information System (INIS)

Dulama, Cristian; Dobrin, Relu; Toma, Alexandru

2001-01-01

There are certain limitations concerning the usage of standard source method for efficiency calibration of gamma - ray spectrometers measuring in extended geometry. These limitations arise from the great diversity of forms, dimensions and densities of the objects which are to be measured. One of the steps in fuel fabrication cycle is the radioactive waste conditioning. At Institute for Nuclear Research INR a radioactive waste management facility operates both for its own purposes and for providing external services. This facility is able to perform conditioning of liquid and solid wastes for interim storage. During the waste conditioning operations there are certain stages when the radioactive measurement of the storage drums is demanded. In order to be able to establish the radioactive content within storage drums during the various procedures that are performed on them at our waste treatment facility we designed and manufactured a mobile equipment for 'in situ' spectrometry. A portable high purity germanium detector was used together with a compact workstation Canberra INSPECTOR incorporating a multi-channel analyzer, a spectroscopic amplifier and a high voltage power supply. Spectral data are processed on-line with a SubNote IBM 486 compatible PC using GeniePC, an OS/2 based spectroscopy software from Canberra. A compact, modular lead housing for the detector was designed and manufactured at INR, using uncontaminated Pb and an inner layer of copper. In front of the detector a lead collimator with cylindrical hole was used to reduce the range of variation for incidence angle. Hence several collimators were manufactured with 10, 20, 40 and 60 mm diameter holes to be able to ensure a proper counting rate in a large range of drum's specific activities by simply changing the collimator. For the efficiency calibration of the spectrometric chain a computer program was written, based on a Monte Carlo algorithm, using a semiempirical method to determinate the effective

Radioactive implant induced x-ray emission technique for noninvasive determination of iodine content in thyroid: experimental study

Energy Technology Data Exchange (ETDEWEB)

Amano, R; Ando, A; Hiraki, T [Kanazawa Univ. (Japan). School of Allied Medical Professions; Tonami, N; Hisada, K [Kanazawa Univ. (Japan). School of Medicine

1984-02-01

A new technique, radioactive implant x-ray emission spectrometry to determine the in vivo iodine content of the human thyroid is proposed. The variations of counting rate and effective excitation efficiencies of I Ksub(..cap alpha..) (28.6 keV) with iodine content, thyroid volume and skin-thyroid distance were studied for the /sup 201/Tl source to examine the properties of excitation and photon attenuation. As a result, the gland depth and volume could be estimated from the peak ratios of 30.7 keV/167.6 keV and 28.6 keV/167.6 keV. Using a 1 MBq /sup 201/Tl implant source, the detectable minimum iodine concentration found was approximately 70 ..mu..g/g for 2000 s measuring time in the phantom experiment. The effectiveness of the RIXE technique is discussed. It was concluded that the /sup 201/Tl RIXE spectrometry might serve to determine the in vivo iodine content of the human thyroid.

Burn-up measurements coupling gamma spectrometry and neutron measurement

Energy Technology Data Exchange (ETDEWEB)

Toubon, H.; Pin, P. [AREVA/CANBERRA, 1 rue des Herons, 78182 St Quentin-en-Yvelines Cedex (France); Lebrun, A. [IAEA, Wagramer Strasse 5, PO Box 100, Vienna (Austria); Oriol, L.; Saurel, N. [CEA Cadarache, 13108 Saint Paul Lez Durance Cedex (France); Gain, T. [AREVA/COGEMA Reprocessing Business Unit, La Hague, 50444 Beaumont Hague Cedex (France)

2006-07-01

The need to apply for burn-up credit arises with the increase of the initial enrichment of nuclear fuel. When burn-up credit is used in criticality safety studies, it is often necessary to confirm it by measurement. For the last 10 years, CANBERRA has manufactured the PYTHON system for such measurements. However, the method used in the PYTHON itself uses certain reactor data to arrive at burn-up estimates. Based on R and D led by CEA and COGEMA in the framework of burn-up measurement for burn-up credit and safeguards applications, CANBERRA is developing the next generation of burn-up measurement device. This new product, named SMOPY, is able to measure burn-up of any kind of irradiated fuel assembly with a combination of gamma spectrometry and passive neutron measurements. The measurement data is used as input to the CESAR depletion code, which has been developed and qualified by CEA and COGEMA for burn-up credit determinations. In this paper, we explain the complementary nature of the gamma and neutron measurements. In addition, we draw on our previous experience from PYTHON system and from COGEMA La Hague to show what types of evaluations are required to qualify the SMOPY system, to estimate its uncertainties, and to detect discrepancies in the fuel data given by the reactor plant to characterize the irradiated fuel assembly. (authors)

Burn-up measurements coupling gamma spectrometry and neutron measurement

International Nuclear Information System (INIS)

Toubon, H.; Pin, P.; Lebrun, A.; Oriol, L.; Saurel, N.; Gain, T.

2006-01-01

The need to apply for burn-up credit arises with the increase of the initial enrichment of nuclear fuel. When burn-up credit is used in criticality safety studies, it is often necessary to confirm it by measurement. For the last 10 years, CANBERRA has manufactured the PYTHON system for such measurements. However, the method used in the PYTHON itself uses certain reactor data to arrive at burn-up estimates. Based on R and D led by CEA and COGEMA in the framework of burn-up measurement for burn-up credit and safeguards applications, CANBERRA is developing the next generation of burn-up measurement device. This new product, named SMOPY, is able to measure burn-up of any kind of irradiated fuel assembly with a combination of gamma spectrometry and passive neutron measurements. The measurement data is used as input to the CESAR depletion code, which has been developed and qualified by CEA and COGEMA for burn-up credit determinations. In this paper, we explain the complementary nature of the gamma and neutron measurements. In addition, we draw on our previous experience from PYTHON system and from COGEMA La Hague to show what types of evaluations are required to qualify the SMOPY system, to estimate its uncertainties, and to detect discrepancies in the fuel data given by the reactor plant to characterize the irradiated fuel assembly. (authors)

Deep underground measurements of 60Co in steel exposed to the Hiroshima atomic bomb explosion.

Science.gov (United States)

Hult, Mikael; Gasparro, Joël; Vasselli, Roberto; Shizuma, Kiyoshi; Hoshi, Masaharu; Arnold, Dirk; Neumaier, Stefan

2004-01-01

When using gamma-ray spectrometry performed deep underground, it is possible to measure 60Co activities down to 0.1 mBq in steel samples of some 100 g without any pre-concentration. It is thus still possible to measure 60Co induced by neutrons from the atomic bomb explosion in Hiroshima in pieces of steel collected at distances up to about 1200 m slant range. The results of non-destructive measurements of eight steel samples are compared with the 1986 Dose Re-Evaluation (DS86) model calculations.

Deep underground measurements of 60Co in steel exposed to the Hiroshima atomic bomb explosion

International Nuclear Information System (INIS)

Hult, Mikael; Gasparro, J.Joeel; Vasselli, Roberto; Shizuma, Kiyoshi; Hoshi, Masaharu; Arnold, Dirk; Neumaier, Stefan

2004-01-01

When using gamma-ray spectrometry performed deep underground, it is possible to measure 60 Co activities down to 0.1 mBq in steel samples of some 100 g without any pre-concentration. It is thus still possible to measure 60 Co induced by neutrons from the atomic bomb explosion in Hiroshima in pieces of steel collected at distances up to about 1200 m slant range. The results of non-destructive measurements of eight steel samples are compared with the 1986 Dose Re-Evaluation (DS86) model calculations

Excess free volume in metallic glasses measured by X-ray diffraction

International Nuclear Information System (INIS)

Yavari, Alain Reza; Moulec, Alain Le; Inoue, Akihisa; Nishiyama, Nobuyuki; Lupu, Nicoleta; Matsubara, Eiichiro; Botta, Walter Jose; Vaughan, Gavin; Di Michiel, Marco; Kvick, Ake

2005-01-01

In crystalline materials, lattice expansion as measured by diffraction methods differs from the expansion of the sample dimensions as measured by dilatometry, due to the contribution of thermal vacancies to the latter. We have found that in glassy materials and metallic glasses in particular, this is not the case for the contribution of free volume. These findings are the first direct experimental confirmation of simulation results indicating that atomic size holes are unstable in glasses such that free volume is dispersed randomly. This allows direct measurement of excess free volume in glasses using diffraction methods in place of dilatometry, which is difficult to use once the sample softens at the glass transition temperature T g and above. Quenched-in and deformation-induced free-volume ΔV f were measured by X-ray diffraction in transmission during heating using synchrotron light. The measured thermal expansion coefficients α th were the same as in dilatometry. The glass transition T g appeared as a break in the value of α th at T g . The 'change-of-slope method' was applied to the kinetics of relaxation to derive the activation energy for the free-volume annihilation process

Surface analysis of WC--Co composite materials (2) Quantitative Auger electron spectrometry

International Nuclear Information System (INIS)

Tongson, L.L.; Biggers, J.V.; Dayton, G.O.; Bind, J.M.; Knox, B.E.

1978-01-01

The unique sensitivity of Auger electron spectrometry (AES) to combined carbon has been exploited in measuring the surface compositions of hot-pressed, conventionally sintered and mixed powders of WC--Co composite materials. AES sensitivity factors for tungsten and carbon (in WC) relative to cobalt were determined. The concentrations of the major elements in hot-pressed samples measured with AES using the relative sensitivity method were compared to those obtained independently by electron microprobe (EMP) and x-ray fluorescence (XRF) techniques. Corollary studies using ion scattering spectrometry (ISS) showed the absence of (1) matrix effects in the AES measurements, (2) preferential sputtering during ion bombardment, and (3) deposition of the easier-to-sputter component (cobalt) onto WC

Porosity measurement of amorphous materials by gamma ray transmission; Medida de porosidade de materiais amorfos por transmissao de raios gama

Energy Technology Data Exchange (ETDEWEB)

Poettker, Walmir Eno

2000-07-01

In this work it is presented the measurement of the total porosity of TRe soil, Sandstone Berea rocks and porous ceramics samples. For the determination of the total porosity, the Arquimedes method (conventional) and the gamma ray transmission methodology were employed. The porosity measurement using the gamma methodology has a significant advantage respect to the conventional method due to the fast and non-destructive determination, and also for supplying results with a greater characterization in small scales, in relation to the heterogeneity of the porosity. The conventional methodology presents good results only for homogeneous samples. The experimental set up for the gamma ray transmission technique consisted of a {sup 241} Am source (59,53 keV), a NaI (Tl) scintillation detector, collimators, a XYZ, micrometric table and standard gamma spectrometry electronics connected to a multichannel analyser. (author)

Improvements in Applied Gamma-Ray Spectrometry with Germanium Semiconductor Detector

Energy Technology Data Exchange (ETDEWEB)

Brune, D; Hellstroem, S [AB Atomenergi, Nykoeping (Sweden); Dubois, J [Chalmers University of Technology, Goeteborg (Sweden)

1965-01-15

A germanium semi-conductor detector has in the present investigation been used in four cases of applied gamma-ray spectrometry. In one case the weak-activity contribution of Cs{sup 134} in Cs{sup 137} standard sources has been determined. The second case concerns the determination of K{sup 42} in samples of biological origin containing strong Na{sup 24} activities. In the third case the Nb{sup 94} and Nb{sup 95} activities from neutron-irradiated niobium foils used in the dosimetry of high neutron fluxes with long exposure times have been completely resolved and it has been possible to determine the ratio of the two activities with a high degree of accuracy. Finally, a Zr{sup 95} - Nb{sup 95} source has been analysed in a similar way with respect to its radiochemical composition. The resolution obtained also made possible a determination of the branching ratio of the two gamma-transitions in Zr{sup 95} and of the energies of the gamma-transitions of both nuclides.

KD901G X-ray system to reject contaminants

International Nuclear Information System (INIS)

Shinohara, Hachiro

1995-01-01

Among the complaints to the foods that consumers bought, the proportion of the mixing of alien substances is more than 20%. The number of the cases classified by the kinds of alien substances, and that of minerals and animal substances are shown. The causes of the mixing of alien substances are classified into those due to the mixing in raw materials, production places, processing machines and workers. In case of using primary products as raw materials, the alien substances closely related to those raw materials are difficult to detect, such as bones and hairs in animal meat, fish bones, egg shells and fruit seeds. There are problems and limitation in the inspection of alien substance mixing by visual or touching inspection, metal detectors and the visual inspection of X-ray radiographs. The judgement of the presence of alien substances by automatically processing X-ray radiograph information has been tried one or two-dimensionally. The X-ray alien substance detector KD901G adopted the one-dimensional line sensor type, and its features are shown. The effective introduction of the X-ray alien substance detector, its comparison with metal detectors, and the safety of workers against radiation exposure and the safety of inspected foods are discussed. (K.I.)

Some considerations on the use of gamma spectrometry for Kr-85 determination at gaseous effluents in the nuclear industry and environmental samples

International Nuclear Information System (INIS)

Heras Iniquez, M.C.; Perez Garcia, M.M.; Travesi, A.

1983-01-01

The possibilities of using high resolution gamma ray spectrometry with GeLi semiconductor detector for measured the 0.514 KeV gamma radiation of Kr-B5 la explored, The detection limit of Kr-85 for a measuring time is 4.10 - 4 μCi with a counting time of 1000 minutes in a GeLi detector with a 20% efficiency relative to the INa (Tl). It is concluded that the use of gamma ray spectrometry for measuring the Kr-85 is not useful for environmental samples, but it can be used for the Kr-85 effluents control in Nuclear Stations. (Author) 26 refs

Drill-Core Scanning for Radioelements by Gamma-Ray Spectrometry

DEFF Research Database (Denmark)

Løvborg, Leif; Wollenberg, H.; Rose-Hansen, J.

1972-01-01

A system has been developed for the continuous and stepwise scanning of rock drill cores for gamma-ray spectrometric determinations of uranium, thorium, and potassium. The apparatus accomodates 3- to 4-cm-diameter core as it passes two opposing 2-inch diameter by 3-inch- thick NaI(Tl) detectors, ......, disclosing detailed variations of U and Th. Contents of U and Th determined by scanning of drill core were consistent with the gross gamma-ray counting rates measured in the boreholes. ©1972 Society of Exploration Geophysicists......A system has been developed for the continuous and stepwise scanning of rock drill cores for gamma-ray spectrometric determinations of uranium, thorium, and potassium. The apparatus accomodates 3- to 4-cm-diameter core as it passes two opposing 2-inch diameter by 3-inch- thick NaI(Tl) detectors...

Chemical analysis of refractories by plasma spectrometry

International Nuclear Information System (INIS)

Coutinho, C.A.

1990-01-01

X-ray spectrometry has been, since the last two or three decades, the traditional procedure for the chemical analysis of refractories, due to its high degree of accuracy and speed to produce analytical results. An interesting alternative to X-ray fluorescence is provided by the Inductively Coupled Plasma Spectrometry technique, for those laboratories where wet chemistry facilities are already available or process control is not required at high speed, or investiment costs have to be low. This paper presents results obtained by plasma spectroscopy for the analysis of silico - aluminous refractories, showing calibration curves, precion and detection limits. Considerations and comparisons with X-ray fluorescence are also made. (author) [pt

The determination, by x-ray-fluorescence spectrometry, of gold and uranium on resin

International Nuclear Information System (INIS)

Jacobs, J.J.; Balaes, A.M.E.

1983-01-01

The problems encountered in the determination of gold and uranium that are present simultaneously in a sample of resin were considered, and new background positions, as well as correction factors for background lift and partial spectral overlap, were determined for use in the X-ray-fluorescence measurement of these elements. The agreement between the results obtained by the use of the X-ray-fluorescence method and those obtained by atomic-absorption spectrophotometry were found to be satisfactory. The relative standard deviation in the former measurements is 0,005 at a concentration of 1000 p.p.m., and the working range of the calibrations is 15 to 1000 p.p.m. These limits can be extended by further dilution of the sample. The limits of determination are 6 p.p.m. in the briquette prepared from a sample of resin and 18 p.p.m. in the sample when the maximum mass of the sample is 3 g. The procedure is intended primarily for use in the rapid determination of gold and uranium when no analyses for other elements are required. The time taken for the analysis is 2 hours for 10 samples when 6 standards are used. A computer programme that was developed for the processing of the data is appended as part of a laboratory method

Calculation of “LS-curves” for coincidence summing corrections in gamma ray spectrometry

Science.gov (United States)

Vidmar, Tim; Korun, Matjaž

2006-01-01

When coincidence summing correction factors for extended samples are calculated in gamma-ray spectrometry from full-energy-peak and total efficiencies, their variation over the sample volume needs to be considered. In other words, the correction factors cannot be computed as if the sample were a point source. A method developed by Blaauw and Gelsema takes the variation of the efficiencies over the sample volume into account. It introduces the so-called LS-curve in the calibration procedure and only requires the preparation of a single standard for each sample geometry. We propose to replace the standard preparation by calculation and we show that the LS-curves resulting from our method yield coincidence summing correction factors that are consistent with the LS values obtained from experimental data.

Determination of rubidium and strontium in geological materials by X-Ray fluorescence spectrometry

International Nuclear Information System (INIS)

Roca, M.

1979-01-01

In order to determine whole-rock ages by the Rb/Sr procedure, an X-ray fluorescence spectrometry method for the determination of both elements has been developed. The samples are pressed into boric acid backed and ringed pellets with this material as a binding agent. Matrix corrections are made following the determination od the mass absorption coefficients, based on the intensity of the Compton-scattered peak of MoKα. or MoKβ 1 .3. The U. S. Geological Survey granodiorite GSP-1 is used as a reference standard. Spectral-line interferences have been carefully studied and the empirical correction factors determined. A BASIC language program for calculating the Rb and Sr concentrations and the Rb/Sr ratios has been written. (Author) 7 refs

X-ray scattering measurements from thin-foil x-ray mirrors

DEFF Research Database (Denmark)

Christensen, Finn Erland; BYRNAK, BP; Hornstrup, Allan

1992-01-01

Thin foil X-ray mirrors are to be used as the reflecting elements in the telescopes of the X-ray satellites Spectrum-X-Gamma (SRG) and ASTRO-D. High resolution X-ray scattering measurements from the Au coated and dip-lacquered Al foils are presented. These were obtained from SRG mirrors positioned...... in a test quadrant of the telescope structure and from ASTRO-D foils held in a simple fixture. The X-ray data is compared with laser data and other surface structure data such as STM, atomic force microscopy (AFM), TEM, and electron micrography. The data obtained at Cu K-alpha(1), (8.05 keV) from all...

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

Energy Technology Data Exchange (ETDEWEB)

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

1963-10-15

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

Gamma-ray measurements in uppermost soil profile of a grazing area around Londrina city, Parana State, Brazil

International Nuclear Information System (INIS)

Bastos, Rodrigo O.; Andrello, Avacir C.; Appoloni, Carlos R.

2005-01-01

Using high-resolution .-ray spectrometry, soil profiles were measured to assess the depth distribution of 232 Th, 238 U, 226 Ra, 40 K and 137 Cs. The surveyed soil is the Latossolo Vermelho Distroferrico, clayey texture, in a soft wave relief area used for grazing, near Londrina city, Parana, Brazil. Knowledge of radioelement depth distributions is important to understand their behavior along soil history, and in the same time, give clues about it, from pedogenesis to more recent events, such as weathering, erosion or interaction with biosphere. Five points were sampled, three of them in increment depths of 0 to 5 cm, 5 to 10 cm, 10 to 15 cm, 15 to 20 cm, 20 to 35 cm, and for two of them the increment 35-50 cm was collected either. These totalized 27 samples, each of them dried in open air during 48 hours, sieved through 2 mm mesh, sealed in 1-litre plastic Marinelli beakers, and measured in the laboratory. It was employed a standard gamma ray spectrometry electronic chain, with a 66% relative efficiency HPGe detector. Measurement of the efficiency in the range from 60 to 1800 keV was carried out with certified IAEA 375 soil sample. From the measured γ-ray spectra, activity concentrations were determined for 232 Th (from 15.4 to 25.1 Bq kg -1 ), 238 U (from 11.0 to 18.9 Bq kg -1 ), 226 Ra (from 4.0 to 10.9 Bq kg -1 ), 40 K (from 36.0 to 133.9 Bq kg -1 ) and 137 Cs (from 0.0 to 2.2 Bq kg -1 ). Average values and respective deviations are 21.0 ± 2.6 Bq kg -1 for 232 Th, 13.8 ± 1.7 Bq kg -1 for 238 U, 7.8 ± 1.9 Bq kg -1 for 226 Ra, 72.8 ± 30.5 Bq kg -1 for 40 K, and 0.8 ± 0.8 Bq kg -1 for 137 Cs. Depth distributions of each radioelement are presented and possible relations among activities are analyzed (author)

Hitomi X-ray Observation of the Pulsar Wind Nebula G21.5$-$0.9

OpenAIRE

Hitomi Collaboration; Aharonian, Felix; Akamatsu, Hiroki; Akimoto, Fumie; Allen, Steven W.; Angelini, Lorella; Audard, Marc; Awaki, Hisamitsu; Axelsson, Magnus; Bamba, Aya; Bautz, Marshall W.; Blandford, Roger; Brenneman, Laura W.; Brown, Gregory V.; Bulbul, Esra

2018-01-01

We present results from the Hitomi X-ray observation of a young composite-type supernova remnant (SNR) G21.5$-$0.9, whose emission is dominated by the pulsar wind nebula (PWN) contribution. The X-ray spectra in the 0.8-80 keV range obtained with the Soft X-ray Spectrometer (SXS), Soft X-ray Imager (SXI) and Hard X-ray Imager (HXI) show a significant break in the continuum as previously found with the NuSTAR observation. After taking into account all known emissions from the SNR other than the...

Determination of the Concentration of Radioactive Nuclides of Surface Soils of some Hadhramout's Valleys in Yemen Using Gamma-Ray Spectrometry

International Nuclear Information System (INIS)

Bazohair, A. O.; Bayashoot, A. K.; AL-Shamy, A. A.

2004-01-01

In this research five surface soil samples have been taken from some Hadhramout's valleys in Yemen (Khrid , Arf , Huwayrah , Buwaish, Khirba ) in the years from (1999) to (2002) and analyzed using gamma-ray spectrometry. The spectra of samples were measured using multichannel analyzer (MCA) that was connected with measurement system for this purpose.A high purity germanium(Hp Ge) detector with resolution of (2.11 keV) at gamma-line(1332 keV) of radioactive source(Co-60) used for detecting ( U 238 , Th 232 , K 40 , Cs 137 ) in the samples. The results showed that the average concentration of radioactive nuclides in the samples of uranium ranged from(37.56 Bq/Kg) to(46.58 Bq/Kg) and for thorium ranged from(37.93 Bq/Kg) to(47.28 Bq/Kg) and for potassium ranged from(347.57 Bq/Kg) to(850.10 Bq/Kg) and for cesium ranged from(6.94 Bq/Kg) to(15.86 Bq/Kg) and the measured precision of samples ranged from(4.71%) to (9.23%). (authors)

Deep underground measurements of {sup 60}Co in steel exposed to the Hiroshima atomic bomb explosion

Energy Technology Data Exchange (ETDEWEB)

Hult, Mikael E-mail: mikael.hult@cec.eu.int; Gasparro, J.Joeel; Vasselli, Roberto; Shizuma, Kiyoshi; Hoshi, Masaharu; Arnold, Dirk; Neumaier, Stefan

2004-09-01

When using gamma-ray spectrometry performed deep underground, it is possible to measure {sup 60}Co activities down to 0.1 mBq in steel samples of some 100 g without any pre-concentration. It is thus still possible to measure {sup 60}Co induced by neutrons from the atomic bomb explosion in Hiroshima in pieces of steel collected at distances up to about 1200 m slant range. The results of non-destructive measurements of eight steel samples are compared with the 1986 Dose Re-Evaluation (DS86) model calculations.

Cu,Cr and As determination in preserved woods (Eucalyptus ssp.) by X-ray fluorescence spectrometries; Determinacao de cobre, cromo e arsenio em madeira preservada (Eucalyptus sp.) pelas espectrometrias de fluorescencia de raios X

Energy Technology Data Exchange (ETDEWEB)

Pereira Junior, Sergio Matias

2014-07-01

Brazil produces around 2.2 millions of cubic meters of treated wood to meet the annual demand of railway, electric, rural and construction sectors. The most used wood species are eucalyptus (Eucalyptus ssp.) and pine (Pinus ssp.).The treated woods used for poles, sleepers, fence posts and plywoods should be according to Brazilian norms requirements. The most usual wood preservative products used in Brazil are CCA (chromated copper arsenate) and CCB (copper chromium and boron salt). The analytical methods, such as flame atomic absorption spectrometry (FAAS), plasma inductively coupled optical emission spectrometry (ICPOES) and X-ray fluorescence spectrometry (XRFS) have been used for the analytical control of those treatment processes. In this work, the eucalyptus trees (Eucalyptus ssp) samples was obtained from Minas Gerais State, Brazil, cut plantation areas. Under pressure, eucalyptus wood samples were submitted to different concentration of CCA solution reaching 3.9, 6.7, 9.1, 12.4 and 14.0 kg of CCA by m-³ sapwood retentions. Samples in cylinders and sawdust forms were obtained from treated wood samples. Copper, chromium and arsenic determination was performed using the energy dispersive X-ray fluorescence spectrometry (EDXRFS), portable X-ray fluorescence spectrometry (PXRFS), flame atomic absorption spectrometry (FAAS) and instrumental neutron activation analysis. In this work, the method of analysis, sensitivity, precision and accuracy performances of the related techniques were outlined. (author)

Chlorine determination in (U, Pu)C fuel by total reflection X-ray fluorescence spectrometry

International Nuclear Information System (INIS)

Misra, Nand Lal; Dhara, Sangita; Mudher, Khush Dev Singh; Aggarwal, Suresh K.; Thakur, Uday Kumar; Shah, Dipti; Sawant, R.M.; Ramakumar, K.L.

2007-01-01

A Total Reflection X-ray Fluorescence (TXRF) method for the determination of chlorine in (U,Pu)C has been developed. The method involves calibration of the instrument with standard solutions and validation of TXRF determination of chlorine using synthetic standard solutions. Cl K α line excited with W L α source was used for TXRF determinations of chlorine. Chlorine present in trace amounts in (U,Pu)C samples was first separated by pyro hydrolysis. The evolved chlorine, in form of HCl, was collected in 5 mM NaOH solution. This solution was analyzed for chlorine by Total Reflection X-ray Fluorescence Spectrometry using cobalt as an internal standard. The TXRF detection limit of chlorine was found to be 3.6 pg with sample size of 30 μL. In order to assess the applicability of TXRF method for chlorine determinations in other nuclear materials, one U 3 O 8 trace element standard was also analyzed for chlorine in similar way. The precision of the method was found to be 25% (1 σ) at ng level in most of the cases. (author)

The study of electric erosion treatments of Ni-superalloys by ion-scattering spectrometry and X-ray analysis

International Nuclear Information System (INIS)

Betsofen, S.Ya.; Borisov, A.M.; Sarychev, S.M.; Romanovskij, E.A.; Bakui Ali; Bespalova, O.V.; Kulikauskas, V.S.; Serkov, M.V.; Grigorovich, K.V.

2004-01-01

The study results are reported for a surface layer of a nickel base heat resistant alloy of the following composition, mas.%: Ni-8.2 Cr-10.5 W-15.5 Co-2.4 Mo-1.4 Nb-4.8 Al-0.2 C, after electroerosion. With the use of Rutherford and nuclear backscattering spectrometry and X-ray diffraction analysis it is revealed that melting under electroerosion results in redistribution of alloying elements, enrichment with carbon and occurrence of residual tensile stresses [ru