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Sample records for gamma spectrometric determination

  1. Determination of uranium enrichment by using gamma-spectrometric methods

    International Nuclear Information System (INIS)

    Kutnyj, D.V.; Telegin, Yu.N.; Odejchuk, N.P.; Mikhailov, V.A.; Tovkanets, V.E.

    2009-01-01

    By using commercial analysis programs MGAU (LLNL, USA) and FRAM (LANL, USA) the summary error of gamma-spectrometric uranium enrichment measurements was investigated. Uranium samples with enrichments of 0,71; 4,46 and 20,1 % were measured. The coaxial high purity germanium detector (type GC) and the planar germanium detector (type LEGe) were used as gamma-radiation detectors. It was shown that experimental equipment and mathematical software available in NSC KIPT allow us to measure uranium enrichment by nondestructive method with accuracy of not worse than 2%.

  2. Gamma spectrometric determination of depleted Uranium in Yugoslavia

    International Nuclear Information System (INIS)

    Pantelic, G.; Eremic Savkovic, M.; Javorina, L.; Tanaskovic, I.; Vuletic, V.; Milacic, S.

    2002-01-01

    The radiation protection is very important interdisciplinary research field due to the presence of the radiation in daily life. The systematic examination of radioactive contamination of various environmental samples was established forty years ago in the Institute of Occupational and Radiological Health Dr Dragomir Karajovic for the sake of preventive protection of population and environment from the harmful effect of ionizing radiation. The global sources of radionuclide contamination in our country are the fallout due to previous nuclear testing and the deposition of radionuclides from the region of Chernobyl accident. The contents of radionuclides were determined in aerosol, soil, fallout (wet and dry deposition), rivers, lakes, drinking water, human and animal food. The samples were collected in several locations of the Republic of Serbia and in regular time intervals, according to methods determined by the regulation. The regulations and the monitoring programs were updated after the Chernobyl accident. In the recent time, after the NATO aggression, we analyzed depleted uranium content in the environmental samples. We used high-resolution gamma spectrometry measurements, because of their simplicity and accuracy. Aims of the control were to asses the increase of radioactivity above the natural levels in the immediate and near vicinity of the bomb craters, to asses the corresponding effect of changed natural radioactivity on the health of the population living in these places and finding unexploded depleted uranium bullets

  3. Marine gamma spectrometric survey

    International Nuclear Information System (INIS)

    Kostoglodov, V.V.

    1979-01-01

    Presented are theoretical problems physical and geochemical prerequisites and possibilities of practical application of the method of continuous submarine gamma-spectrometric survey and radiometric survey destined for rapid study of the surface layer of marine sediments. Shown is high efficiency and advantages of this method in comparison with traditional and widely spread in marine geology methods of bottom sediments investigation

  4. Gamma Spectrometric Determination of U, Th, K and Some Geochemical Applications

    International Nuclear Information System (INIS)

    Dodona, A.; Tashko, A.

    2001-01-01

    The application of 'in situ' gamma-spectrometric method (''infinite'' environment), made possible the simultanious determination of U, Th and K. 4 channel gamma-spectrometric analyser with NaI(TI) scintilation counter crystal detector (103 cm 3 φ=50x50mm) was used to determin U, Th(more than 1-2 ppm) and K (more than 1%) in laboratory conditions. The detector was inserted into a lead camera and calibrated for measurement geometry with vessel of ''Marineli'' type of a 17o cm 3 volume. The study of main factors, which influence in the gamma spectrometric measurements, (the technical, physical, geometrical and time parameters) has been carried out. International standards of U, Th, K and internal monitoring standard samples are used for the calibration. External analytical control has been realized by other radiometric and chemical methods. The detection limits ( 1 ppm Th, 2ppm U and 1% K) and the relative errors (17-20% for 1-10 ppm U, Th and 10-15% for more than 10 ppm U, Th and more than 1% K) guarantee a quantitative analysis that may be used successfully in the geochemical studies. Some geochemical applications, based on the content of Th, U and Th/U ratio in rocks samples that we have we have analyzed with this method, are shown in this paper. U, Th and their ratio are used as trace elements to indicate the differences between the acidic magmatic rocks of Albania (Th/U ratio=2-6 and>10). The bimodal character of Th/U scattering in ignimbrides and monzonites (Korabi zone) shows that in addition to the ''normal'' rocks, there are also some ones enriched with Th, So, the differential analysis of Th, U, and K may be used as geochemical exploration criteria for the radioactive and non-radioactive mineralization, such as REE (Rare Earth Elements), phospghorites, bauxites, placers etc. (authors)

  5. Rapid in situ gamma spectrometric determination of fallout radioactivity in the environment. Progress report

    International Nuclear Information System (INIS)

    Zombori, Peter

    1995-01-01

    The main aim of the present CRP is to identify the existing analytical methods and develop new ones, if possible, which provide rapid, reliable, and detailed information on the radioactive contamination of the environment after a major nuclear accident. Gamma spectrometry has long been regarded as one of the most applicable radioanalytical techniques but its use for environmental studies requires some further considerations. There are two possible approaches to measure environmental radioactivity: (a) taking samples of the different environmental media and measuring them in a laboratory or (b) taking the spectrometer to the place of interest and making in situ measurements. In the former case sampling is a crucial factor hindering the rapid analysis while the latter case is not always reliable due to the problems and uncertainties of the measurement interpretation. The application of in situ gamma spectrometry for the determination of environmental radioactivity has become increasingly attractive since the advent of the high resolution semiconductor gamma detectors, especially, more recently, portable high purity Ge diodes (HpGe). The applicability of this technique was very well proved after the Chernobyl reactor accident when in situ spectrometry played an important role in the rapid evaluation of the fall-out situation. Our measurements provided information on the amount and composition of the radioactive contamination of the ground surface already in the first hours. These measurements enabled us to predict the time variation of the environmental radioactivity after the stabilization of the situation. The portability of the system was an important factor in performing a rapid and efficient survey in different parts of the country. A serious disadvantage of this method is, however, that it requires some knowledge about the radionuclide distribution in the soil, which is normally determined by tedious and time consuming sample analysis of the different soil

  6. A computer program for nuclear fuel burnup determination using gamma spectrometric methods

    International Nuclear Information System (INIS)

    Dobrin, Relu; Pavelescu, Margarit

    2010-01-01

    In the end of its service life in the reactor, the fuel needs to be characterized for reasons relating both to safety and economy. The main investigations carried out are oriented towards verifying the fuel cladding integrity and determining the fissile content and the fuel burnup. A computer program for fast burnup evaluation was developed at the Post-Irradiation Examination Laboratory (PIEL) from INR Pitesti, the only laboratory of this kind in Romania. The input data consists, on one hand, of axial and radial gamma-scanning profiles (for the experimental evaluation of the number of nuclei of a given fission product - selected as burnup monitor - in the end of irradiation) and, on the other hand, of the history of irradiation (the time length and relative value of the neutron flux for each step of irradiation). Using the equation for the build-up and decay of the burnup monitor during irradiation the flux value is iteratively adjusted until the calculated number of nucleus is equal to the experimental one. Then the flux value is used in the equations of evolution of the fissile and fertile nuclei to determine the number of fissions and consequently the fuel burnup. The program was successfully used in the analysis of more then one hundred of TRIGA and CANDU-type fuel rods. An experimental result is reported in some details. (authors)

  7. Optimisation of spectrometric gamma-gamma probe configuration using very low radioactivity sources for lead and zinc grade determination in borehole logging

    CERN Document Server

    Asfahani, J

    1999-01-01

    The suitability of spectrometric backscattered gamma-gamma well logging measurements to predict lead and zinc metal equivalent content is demonstrated. A centralised tool employing a gamma-ray source of very low radioactivity (1.8 MBq) is used. The logging tool is tested using sup 1 sup 3 sup 3 Ba and sup 1 sup 3 sup 7 Cs sources with a 37 mm (diameter)x75 mm NaI (TI) scintillation detector. Five source-to-detector configurations were analysed for 18 geophysical models, 13 of which had a borehole diameter of 130 mm and the other 5 had a borehole diameter of 160 mm. Regression analysis on the laboratory logging data for each configuration in order to establish the calibration equation for a lead (Pb) and zinc metal equivalent (ZME) prediction is carried out. The optimum configuration for the logging probe using a sup 1 sup 3 sup 3 Ba source was determined to be 52 mm source-to-detector spacing. This configuration gives the best results for both Pb and ZME grade. The rms deviations for Pb and ZME were 0.33 and ...

  8. Processing of gamma-ray spectrometric logs

    International Nuclear Information System (INIS)

    Umiastowski, K.; Dumesnil, P.

    1984-10-01

    CEA (Commissariat a l'Energie Atomique) has developped a gamma-ray spectrometric tool, containing an analog-to-digital converter. This new tool permits to perform very precise uranium logs (natural gamma-ray spectrometry), neutron activation logs and litho-density logs (gamma-gamma spectrometric logs). Specific processing methods were developped to treate the particular problems of down-hole gamma-ray spectrometry. Extraction of the characteristic gamma-ray peak, even if they are superposed on the background radiation of very high intensity, is possible. This processing methode enables also to obtain geological informations contained in the continuous background of the spectrum. Computer programs are written in high level language for SIRIUS (VICTOR) and APOLLO computers. Exemples of uranium and neutron activation logs treatment are presented [fr

  9. Gamma spectrometric determination of naturally occurring elements in sediment samples of Egypt

    International Nuclear Information System (INIS)

    EL-Sayed, A.A.

    2006-01-01

    Determination of the naturally occurring elements 238 U( 226 Ra), 40 K, 232 Th( 228 Ra) and the fission product 137 Cs in sediments and water in two environmental systems in southern and northern parts of Egypt was made. These ecological systems represent main surface water system, supply drinking water to eastern part of Egypt, and the other is brackish water

  10. Gamma spectrometric analyses of environmental samples at PINSTECH

    International Nuclear Information System (INIS)

    Faruq, M.U.; Parveen, N.; Ahmed, B.; Aziz, A.

    1979-01-01

    Gamma spectrometric analyses of air and other environmental samples from PINSTECH were carried out. Air particulate samples were analyzed by a Ge(Li) detector on a computer-based multichannel analyzer. Other environmental samples were analyzed by a Na(T1) scintillation detector spectrometer and a multichannel analyzer with manual analysis. Concentration of radionuclides in the media was determined and the sources of their production were identified. Age of the fall out was estimated from the ratios of the fission products. (authors)

  11. System for Gamma an X rays fluorescence spectrometric

    International Nuclear Information System (INIS)

    Alonso Abad, D.; Arista Romeu, E.; Bolanos Perez, L. and others

    1997-01-01

    A system for spectrometry of gamma or fluorescence X rays is presented. It sis composed by a Si(Li) semiconductors detector, a charge sensitive preamplifier, a high voltage power supply, a spectrometric amplifier and a monolithic 1024 channels multichannel analyzers or an IBM compatible 4096 channels add - on- card multichannel analyzer. The system can be configured as a 1024 or 4096 channels gamma or fluorescent X rays spectrometer

  12. Gamma spectrometric discrimination of special nuclear materials

    International Nuclear Information System (INIS)

    Dowdall, M.; Mattila, A.; Ramebaeck, H.; Aage, H.K.; Palsson, S.E.

    2012-12-01

    This report presents details pertaining to an exercise conducted as part of the NKS-B programme using synthetic gamma ray spectra to simulate the type of data that may be encountered in the interception of material potentially containing special nuclear materials. A range of scenarios were developed involving sources that may or may not contain special nuclear materials. Gamma spectral data was provided to participants as well as ancillary data and participants were asked, under time constraint, to determine whether or not the data was indicative of circumstances involving special nuclear materials. The situations varied such that different approaches were required in order to obtain the correct result in each context. In the majority of cases participants were able to correctly ascertain whether or not the situations involved special nuclear material. Although fulfilling the primary goal of the exercise, some participants were not in a position to correctly identify with certainty the material involved, Situations in which the smuggled material was being masked by another source proved to be the most challenging for participants. (Author)

  13. Gamma spectrometric discrimination of special nuclear materials

    Energy Technology Data Exchange (ETDEWEB)

    Dowdall, M. [Norwegian Radiation Protection Authority (Norway); Mattila, A. [Radiation and Nuclear Safety Authority, Helsinki (Finland); Ramebaeck, H. [Swedish Defence Research Agency, Stockholm (Sweden); Aage, H.K. [Danish Emergency Management Agency, Birkeroed (Denmark); Palsson, S.E. [Icelandic Radiation Safety Authority, Reykjavik (Iceland)

    2012-12-15

    This report presents details pertaining to an exercise conducted as part of the NKS-B programme using synthetic gamma ray spectra to simulate the type of data that may be encountered in the interception of material potentially containing special nuclear materials. A range of scenarios were developed involving sources that may or may not contain special nuclear materials. Gamma spectral data was provided to participants as well as ancillary data and participants were asked, under time constraint, to determine whether or not the data was indicative of circumstances involving special nuclear materials. The situations varied such that different approaches were required in order to obtain the correct result in each context. In the majority of cases participants were able to correctly ascertain whether or not the situations involved special nuclear material. Although fulfilling the primary goal of the exercise, some participants were not in a position to correctly identify with certainty the material involved, Situations in which the smuggled material was being masked by another source proved to be the most challenging for participants. (Author)

  14. Outdoor spectrometric measurement of gamma source activities

    International Nuclear Information System (INIS)

    Cespirova, I.

    2003-01-01

    Two methods for outdoor activity measurements are described. The one is the in situ measurement method which is based on a proportionality between the flux density of non-dispersed photons of the given energy at the detector site and the specific activity of the relevant radionuclide in soil. The other method, for the monitoring of large areas, uses the spectrometric IRIS system (Integrated Radiation Information System), located on a helicopter for aerial monitoring or in a car for terrestrial measurement. (P.A.)

  15. Gamma spectrometric system based on the personal computer Pravetz-83

    International Nuclear Information System (INIS)

    Yanakiev, K; Grigorov, T.; Vuchkov, M.

    1985-01-01

    A gamma spectrometric system based on a personal microcomputer Pravets-85 is described. The analog modules are NIM standard. ADC data are stored in the memory of the computer via a DMA channel and a real-time data processing is possible. The results from a series of tests indicate that the performance of the system is comparable with that of comercially avalable computerized spectrometers Ortec and Canberra

  16. Gamma spectrometrical examination of irradiated fuel

    International Nuclear Information System (INIS)

    Kristof, Edvard; Pregl, Gvido

    1988-01-01

    Gamma scanning is the only non-destructive technique for quantitative measuring of fission or activation products in spent fuel. The negligence of local variation of the linear attenuation coefficient of gamma rays in the irradiated fuel remains the main source of systematic error. To eliminate it we combine the (single) emission gamma ray scanning technique with a transmission measurement. Mathematical procedure joined with the experiment is particularly convenient for fuel elements of circular cross-section. In such a manner good results are obtainable even for relatively small number of measuring data. Accomplished routines enable to esteem the finite width of the collimation slit. The experiment has been partially automated. Trial measurements were carried out, and the measured data were successfully processed

  17. Actively shielded low level gamma - spectrometric system

    International Nuclear Information System (INIS)

    Mrdja, D.; Bikit, I.; Forkapic, S.; Slivka, J.; Veskovic, M.

    2005-01-01

    The results of the adjusting and testing of the actively shielded low level gamma-spectrometry system are presented. The veto action of the shield reduces the background in the energy region of 50 keV to the 2800 keV for about 3 times. (author) [sr

  18. Gamma-spectrometric examination of hot particles emitted during the Chernobyl accident

    International Nuclear Information System (INIS)

    Balashazy, I.; Szabadine-Szende, G.; Loerinc, M.; Zombori, P.

    1987-05-01

    Ge(Li) gamma-spectrometric examination of hot particles prepared from air filtered dust of Budapest air after the Chernobyl accident is presented. The method of separating hot particles is described and their concentration in the air is determined. The radioactive isotope composition of hot particles is discussed and compared with that of dust samples. Finally, the inhalation probability and radiation burden of hot particles are evaluated. (author)

  19. Malevolent use of radioactive materials: An international exercise in the analysis of gamma-spectrometric data

    DEFF Research Database (Denmark)

    Dowdall, M.; Andersson, Kasper Grann; Palsson, S.E.

    2010-01-01

    with isotopes and activities that present significant challenges with respect to identification and quantification using gamma ray spectrometry. The MALRAD international exercise was designed to provide a practice opportunity for authorities and laboratories to work with synthetic gamma-spectrometric data...

  20. Gamma spectrometric method for measuring natural radioactivity of building materials

    International Nuclear Information System (INIS)

    Toth, A.; Feher, I.

    1976-11-01

    The natural 232 Th, 226 Ra and 40 K concentrations of building materials were determined by gamma spectrometry. Altogether 121 samples from all over Hungary, one from each factory producing building materials, were examined. The presented data had preliminary character. The results were compared to the relating ones from abroad. (Sz.N.Z.)

  1. Characterization of HPGe gamma spectrometric detectors systems for Instrumental Neutron Activation Analysis (INAA) at the Colombian Geological Survey

    Energy Technology Data Exchange (ETDEWEB)

    Sierra, O., E-mail: osierra@sgc.gov.co; Parrado, G., E-mail: gparrado@sgc.gov.co; Cañón, Y.; Porras, A.; Alonso, D.; Herrera, D. C.; Peña, M., E-mail: mlpena@sgc.gov.co; Orozco, J. [Colombian Geological Survey, Nuclear Affairs Technical Division, Neutron Activation Analysis Laboratory, Bogota D. C. (Colombia)

    2016-07-07

    This paper presents the progress made by the Neutron Activation Analysis (NAA) laboratory at the Colombian Geological Survey (SGC in its Spanish acronym), towards the characterization of its gamma spectrometric systems for Instrumental Neutron Activation Analysis (INAA), with the aim of introducing corrections to the measurements by variations in sample geometry. Characterization includes the empirical determination of the interaction point of gamma radiation inside the Germanium crystal, through the application of a linear model and the use of a fast Monte Carlo N-Particle (MCNP) software to estimate correction factors for differences in counting efficiency that arise from variations in sample density between samples and standards.

  2. Ground gamma-ray spectrometric studies of El-Sahu area, southwestern Sinai, Egypt

    Science.gov (United States)

    Abdrabboh, Ahmad M.

    2017-12-01

    Based on the previous airborne gamma-ray spectrometric study carried out in southwestern Sinai area, El Sahu area was selected for detail ground gamma-ray spectrometric survey. This area is considered as a good target for radioactive mineral exploration. The study area is exposed in a Paleozoic basin covered by different rocks (ranging from Precambrian to Quaternary). The ground gamma-ray spectrometric survey has been conducted along the study area through random survey. The resultant gamma-ray spectrometric maps show different levels of radioactivity over the studied area, which reflect contrasting radioelement contents for the exposed various rock types. The studied area possesses total count ranging from 2.6 to 326 Ur, 0.1 to 2.8% K, 1.7 to 316 ppm eU and 0.9 to 47.5 ppm eTh. The highest uranium concentrations are located in the northern and southern parts of El Sahu area. They are mainly associated with Um Bogma Formation occurrences. Uranium ratio maps (eU/K and eU/eTh) as well as ternary maps show sharp increase of eU content over both potassium and thorium contents associated with the ENE and NNW trends in Um Bogma Formation, indicating an increase in the U-potentiality than the surrounding rocks. This indicates that the mineralization in the study area may be structurally-controlled.

  3. Calibration facilities of airborne, surface and borehole gamma ray spectrometric survey systems

    International Nuclear Information System (INIS)

    Sarma, C.V.R.; Raghuwanshi, S.S.; Sreehari, R.; Johri, N.K.

    2009-01-01

    The gamma-ray spectrometric surveys for uranium exploration are based upon the detection of gamma-rays emitted by the primordial radio nuclides of Uranium (Bi-214), Thorium (Tl-208) and K-40. However, the instrumentation with gamma radiation detectors for surface, airborne, borehole surveys requires to be calibrated for processing of field acquired data. Various calibration procedures are being adopted for this purpose in Atomic Minerals Directorate for Exploration and Research in India and elsewhere in the world. The airborne and portable gamma-ray spectrometric survey systems are calibrated on indigenously constructed and suitably spiked concrete calibration pads at the Civil Airport at Nagpur, India over very low activity zone of Deccan traps. Using these pads sensitivities and Compton scattering factors are computed for these systems. For the calibration of gamma-ray borehole logging probes, concretized boreholes have been constructed at premises of AMD Headquarters Hyderabad which are called the primary standards. The concentrations of these standards and results found for the sensitivities of different probes and systems are given in Table 1 thru Table 5. These calibration standards at Hyderabad and Nagpur are now the National facilities and are being constantly used for calibration purposes not only for the gamma ray spectrometers designed by AMD, but also for the imported gamma ray spectrometric systems acquired by various other organizations in India. This paper describes the details of these calibration facilities. There are two more calibration facilities for airborne gamma-ray spectrometric survey systems which are located at Devarakonda, A.P. and Mahalarbadi in Maharashtra, The concentrations of U, Th, K of Devarakonda Test Strip, A.P. are given in Table 2. (author)

  4. Spectrometric determination of ammonium-nitrogen with quinol in ...

    African Journals Online (AJOL)

    Quinol is proposed as a reagent for the spectrometric determination of ammonium-nitrogen (NH4+-N) in aqueous medium. Quinol forms a pink complex with ammonium salt in aqueous medium. Hydrogen peroxide is needed for colour accentuation. The quinol/ammonium charge transfer complex has absorption maximum ...

  5. Partial least squares−near infrared spectrometric determination of ...

    African Journals Online (AJOL)

    Partial least squares−near infrared spectrometric determination of ethanol in distilled alcoholic beverages. ... Derivative, mean centering and subtracting minimum value were used as data treatment techniques for noise reduction and baseline correction. Mean centering has given the best partial least squares model with ...

  6. Gamma spectrometric characterization of refractory products used in Turkey

    International Nuclear Information System (INIS)

    Turhan, Şeref; Gündüz, Yunus; Varinlioğlu, Ahmet

    2014-01-01

    This is the first detailed study related to the radiometric characterization of refractory materials produced for use in the industries of iron–steel, cement and glass manufacturing in Turkey. In this study, the activity concentrations of 226 Ra, 232 Th and 40 K naturally occurring in 52 refractory material samples collected from Turkey's leading refractory factories were measured by using a gamma spectrometer with HPGe detector. Results show that the natural radioactivity of refractory material samples varies depending on raw material. The values of the activity concentrations of 226 Ra, 232 Th and 40 K measured in the refractory brick and concrete samples varied from 1.3 to 384.2 Bq kg −1 (average: 173.5±20.2 Bq kg −1 ), 2.9 to 392.9 Bq kg −1 (average: 176.7±20.8 Bq kg −1 ) and 18.9 to 679.6 Bq kg −1 (average: 130.4±23.9 Bq kg −1 ) and 24.0 to 158.2 Bq kg −1 (average: 73.3±10.5 Bq kg −1 ), 25.0 to 134.4 Bq kg −1 (average: 76.3±10.8 Bq kg −1 ) and 31.0 to 480.0 Bq kg −1 (average: 172.8±40.5 Bq kg −1 ), respectively. The activity concentrations of 226 Ra and 232 Th measured in fireclay brick and high alumina brick samples are significantly higher than the average values of earth's crust. - Highlights: • The study determines the radiometric characterization of refractory products. • The activity concentrations of 226 Ra, 232 Th and 40 K in refractory products are measured by the gamma-ray spectrometer. • Refractory magnesite brick samples contain low levels of 226 Ra 232 Th and 40 K. • Refractory high alumina brick samples contain high levels of 226 Ra and 232 Th depending on the raw materials. • Refractory concrete samples contain high levels of 226 Ra and 232 Th depending on the raw materials

  7. Graphite furnace atomic absorption spectrometric determination of ...

    African Journals Online (AJOL)

    A method for the determination of trace amount of cadmium ion after preconcentration by extracting its dithizone complex into molten naphthalene was developed. Several experimental conditions such as pH of the solution, stirring time, the amounts of naphthalene, standing time and volume of the solution were optimized.

  8. Spectrometric gamma radiation of shale cores applied to sweet spot discrimination in Eastern Pomerania, Poland

    Science.gov (United States)

    Skupio, Rafal; de Alemar Barberes, Gabriel

    2017-12-01

    This paper describes the application and calculation of hydrocarbon anomalies in two different boreholes located in Eastern Pomerania (northern Poland). Spectrometric data from borehole geophysical probe (borehole 1) and portable gamma logger (borehole 2) were used to analyze shale formations. The results from borehole 1 presented a statistically significant, moderate correlation between calculated hydrocarbon anomalies and hydrocarbon saturation data obtained from well log interpretation. Borehole 2 has been analyzed focusing on the gamma radiation of the core samples, and the positive results of borehole 1. Hydrocarbon anomalies calculated from spectral gamma radiation are reliable indicators of sweet spots, based solely on a cursory evaluation of core measurements. These preliminary information acquired from gamma-ray measurements could help increase sampling precision of further geochemical analysis.

  9. Photometric and emission-spectrometric determination of boron in steels

    International Nuclear Information System (INIS)

    Thierig, D.

    1982-01-01

    A method for the photometric determination of boron in unalloyed and alloyed steels is described, in which Curcumine is used as reagent. A separation of boron is not necessary. Limit of detection: 0.0003% B. The decomposition of boron nitride in the steel is achieved by heating the whole sample in fuming sulphuric acid/phosphoric acid. For the emission spectrometric investigation of solid steel samples and for the spectrochemical analysis of solutions with plasma excitation working parameters are given and possibilities of interferences are demonstrated. (orig.) [de

  10. Photometric and emission-spectrometric determination of boron in steels

    Energy Technology Data Exchange (ETDEWEB)

    Thierig, D.

    1982-01-01

    A method for the photometric determination of boron in unalloyed and alloyed steels is described, in which Curcumine is used as reagent. A separation of boron is not necessary. Limit of detection: 0.0003% B. The decomposition of boron nitride in the steel is achieved by heating the whole sample in fuming sulphuric acid/phosphoric acid. For the emission spectrometric investigation of solid steel samples and for the spectrochemical analysis of solutions with plasma excitation working parameters are given and possibilities of interferences are demonstrated.

  11. The application study on the prospecting for gold by car-borne gamma-ray spectrometric method in northern Hebei and other areas

    International Nuclear Information System (INIS)

    Ma Zhongxiang; Liu Tengyao; Zhang Peng; Lu Shili; Zhai Yugui; Ma Yanfang

    1995-01-01

    The prospecting method for gold by car-borne gamma-ray spectrometric survey is a new geophysical and geochemical technique in the search for concealed gold deposits which can be used to effectively predict the regional gold metallogenetic potential area. The method of car-borne gamma-ray spectrometric survey was adopted and 63416 data at gamma-ray spectrometric measuring sites from rock masses (or strata) in northern Hebei and other areas (49100 km 2 ) are obtained. On the basis of the size of geological bodies, the sliding filtering technique was applied to process the gamma-ray spectrometric data from regional geological bodies and maps showing the parameter distribution characteristics were plotted (11 sheets). In accordance with the thorough on the distribution characteristics of gamma-ray spectrometric parameters that reflect the regional geological environment of gold metallogenesis, a set of gamma-ray spectrometric combination parameters in correlation with regional gold metallogenesis has been established and the characteristic information of gamma-ray spectrometric parameters has been extracted. Combined with geological information, the gold metallogenetic geological environment in the working area was studied, and two potential areas were predicted. After verification, gold mineralization was encountered in some areas. The study results show that the car-borne gamma-ray spectrometric method used for regional gold prospecting is a rapid, economical and effective one

  12. A gamma-gamma coincidence spectrometric method for rapid characterization of uranium isotopic fingerprints

    International Nuclear Information System (INIS)

    Weihua Zhang; Jing Yi; Pawel Mekarski; Kurt Ungar; Barry Hauck; Kramer, G.H.

    2011-01-01

    This paper reports on initial efforts for uranium isotopic analysis using gamma-rays and X-ray fluorescence coincidence. In this study, a gamma-gamma coincidence spectrometry was developed. The spectrometry consists of two NaI(Tl) scintillators and XIA LLC Digital Gamma Finder (DGF)/Pixie-4 software and card package. The developed spectrometry was optimized according to the considerations of output count rate and gamma peak energy resolution. It has been demonstrated that the spectrometry provides an effective method of assessing the content of uranium isotopes for nuclear materials. The main advantages of this approach over the conventional gamma spectrometry include the fact that 235 U enrichment can be graphically characterized by its unique coincidence 'fingerprints'. The method could be further developed for fast uranium isotope verification with an established gamma-gamma coincidence spectral imaging library by various nuclear materials. (author)

  13. Determination of Mass Spectrometric Sensitivity of Different Metalloporphyrin Esters Relative to Porphyrin Ester

    DEFF Research Database (Denmark)

    Larsen, Elfinn; Egsgaard, Helge; Møller, J.

    1977-01-01

    Quantitative determination of metalloporphyrin contamination in preparations of biologically important porphyrins was achieved mass spectrometrically by application of the integrated ion current technique. For this purpose, the relative molecular ion sensitivities of the contaminating metal...... of calibration samples, including complex formation and the mass spectrometric methodology, is described and discussed....

  14. Determination of iodine to compliment mass spectrometric measurements

    International Nuclear Information System (INIS)

    Hohorst, F.A.

    1994-11-01

    The dose of iodine-129 to facility personnel and the general public as a result of past, present, and future activities at DOE sites is of continuing interest, WINCO received about 160 samples annually in a variety of natural matrices, including snow, milk, thyroid tissue, and sagebrush, in which iodine-129 is determined in order to evaluate this dose, Currently, total iodine and the isotopic ratio of iodine-127 to iodine-129 are determined by mass spectrometry. These two measurements determine the concentration of iodine-129 in each sample, These measurements require at least 16 h of mass spectrometer operator time for each sample. A variety of methods are available which concentrate and determine small quantities of iodine. Although useful, these approaches would increase both time and cost. The objective of this effort was to determine total iodine by an alternative method in order to decrease the load on mass spectrometry by 25 to 50%. The preparation of each sample for mass spectrometric analysis involves a common step--collection of iodide on an ion exchange bed. This was the focal point of the effort since the results would be applicable to all samples

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

    International Nuclear Information System (INIS)

    Udoh, Anthony P.

    2000-01-01

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

  16. An Attempt to automate the lithological classification of rocks using geological, gamma-spectrometric and satellite image datasets

    International Nuclear Information System (INIS)

    Fouad, M. K.; Mielik, M. L.; Gharieb, A. N.

    2004-01-01

    The present study aims essentially at proving that the application of the integrated airborne gamma spectrometric and satellite image data is capable of refining the mapped surface geology, and identification of anomalous zones of radioelement content that could provide favorable exploration targets for radioactive mineralizations.The application of the appropriate statistical technique to correlate between satellite image data and gamma-spectrometric data is of great significance in this respect. Experience shows that Landsat T M data in 7 spectral bands are successfully used in such studies rather than MSS. Multivariate statistical analysis techniques are applied to airborne spectrometric and different spectral Landsat T M data. Reduction of the data from n-dimensionality, both qualitatively as color composite image, and quantitatively, as principal component analysis, is performed using some statistical control parameters. This technique shows distinct efficiency in defining areas where different lit ho facies occur. An area located at the north of the Eastern Desert of Egypt, north of Hurgada town, was chosen to test the proposed technique of integrated interpretation of data of different physical nature. The reduced data are represented and interpreted both qualitatively and quantitatively. The advantages and limitations of applying such technique to the different airborne spectrometric, and Landsat T M data are identified. (authors)

  17. Study of the spectrometric performances of monolithic CdZnTe / CdTe gamma ray detectors

    International Nuclear Information System (INIS)

    Gros d'Aillon, E.

    2005-11-01

    Pixelated monolithic CdTe/CdZnTe semiconductor gamma ray detectors are brought to replace scintillation detectors for medical applications, notably for single photon emission computed tomography (SPECT). In addition to compactness, they present better spectrometric performances: energy resolution, detection efficiency, and spatial resolution. Moreover, the photons depth of interaction in the crystal can be measured. This work aimed in studying experimentally and by simulation the correlations between anodes pitch, material physic properties (resistivity and electron transport properties), and detectors spectrometric performances. We have compared several methods of measuring the photon interaction depth, and have obtained an energy resolution ranging from 1.7% to 7% at 122 keV, according to material, for 5 mm thick detectors. Charge sharing between adjacent anodes has been studied and a measured data processing is proposed. (author)

  18. Spectrometric methods for the determination of chlorine in crude oil and petroleum derivatives — A review

    International Nuclear Information System (INIS)

    Doyle, Adriana; Saavedra, Alvaro; Tristão, Maria Luiza B.; Mendes, Luiz A.N.; Aucélio, Ricardo Q.

    2013-01-01

    Chlorine determination in crude oil is made in order to guarantee that the oil does not contain levels of this element that might cause damages in the oil processing equipment. In petroleum products, the determination of chlorine is made, for instance, to evaluate if there are proper concentrations of organochloride compounds, which are used as additives. Such determinations are currently performed following official guidelines from the ASTM International and from the United States Environmental Protection Agency as well as protocols indicated by the Universal Oil Products. X-ray fluorescence spectroscopy plays an important role in many of these official methods. In contrast, other spectrometric methods based on optical and mass detection are plagued by limitations related to both the fundamental characteristics of non-metals and to the complex sample matrices, which reflects in the small number of articles devoted to these applications. In this review, the current status of the spectrometric methods, especially the role played by X-ray fluorescence spectrometry, is evaluated in terms of the determination of chlorine in crude oil and petroleum derivatives. Comparison of the performance of the methods, limitations and potential new approaches to ensure proper spectrometric determinations of chlorine is indicated. - Highlights: • Critical evaluation of spectrometric methods for chlorine in petroleum products. • Reviews on element determination in petroleum have not address the case of chlorine. • Peculiarities of the spectrometric determination of Cl in petroleum are discussed. • The spectrometric approaches are detailed and compared to the official methods. • New trends in chlorine determination in petroleum products are indicated

  19. Spectrometric methods for the determination of chlorine in crude oil and petroleum derivatives — A review

    Energy Technology Data Exchange (ETDEWEB)

    Doyle, Adriana [Department of Chemistry, Pontifical Catholic University of Rio de Janeiro, Rua Marquês de São Vicente 225, Gávea, Rio de Janeiro, RJ 22451-900 (Brazil); Saavedra, Alvaro; Tristão, Maria Luiza B.; Mendes, Luiz A.N. [Leopoldo Américo Miguez de Mello Research Center — Petrobras (CENPES), Cidade Universitária, Quadra 7, Ilha do Fundão, Rio de Janeiro 21949-900 (Brazil); Aucélio, Ricardo Q., E-mail: aucelior@puc-rio.br [Department of Chemistry, Pontifical Catholic University of Rio de Janeiro, Rua Marquês de São Vicente 225, Gávea, Rio de Janeiro, RJ 22451-900 (Brazil)

    2013-08-01

    Chlorine determination in crude oil is made in order to guarantee that the oil does not contain levels of this element that might cause damages in the oil processing equipment. In petroleum products, the determination of chlorine is made, for instance, to evaluate if there are proper concentrations of organochloride compounds, which are used as additives. Such determinations are currently performed following official guidelines from the ASTM International and from the United States Environmental Protection Agency as well as protocols indicated by the Universal Oil Products. X-ray fluorescence spectroscopy plays an important role in many of these official methods. In contrast, other spectrometric methods based on optical and mass detection are plagued by limitations related to both the fundamental characteristics of non-metals and to the complex sample matrices, which reflects in the small number of articles devoted to these applications. In this review, the current status of the spectrometric methods, especially the role played by X-ray fluorescence spectrometry, is evaluated in terms of the determination of chlorine in crude oil and petroleum derivatives. Comparison of the performance of the methods, limitations and potential new approaches to ensure proper spectrometric determinations of chlorine is indicated. - Highlights: • Critical evaluation of spectrometric methods for chlorine in petroleum products. • Reviews on element determination in petroleum have not address the case of chlorine. • Peculiarities of the spectrometric determination of Cl in petroleum are discussed. • The spectrometric approaches are detailed and compared to the official methods. • New trends in chlorine determination in petroleum products are indicated.

  20. Measurement of fission yields for 232-Th (n,f) at 14,7 MeV by direct gamma spectrometric method

    International Nuclear Information System (INIS)

    Chouak, K.; Berrada, M.; Embarech, K.

    1994-01-01

    Fission yields for the reaction 232-Th (n,f) were measured at 14,7 MeV using the activation technique with direct gamma spectrometric method. Neutrons were produced via the T(d,n) sup 4 He reaction. The neutron fluences were determined relative to the well-known sup 2 sup 7 Al(n,p) sup 2 sup 7 Mg or sup 2 sup 7 Al(n,alpha) sup 2 sup 4 Na cross section, according to the irradiation time. Yields of fission products were determined by measuring the induced gamma ray activities of the irradiated Th foils, using a calibrated Ge(Li) detector. All necessary corrections were taken into account: self absorption, coincidence losses and natural gamma rays. Fifty six cumulative yields were measured and only twenty one corresponding results were found in the literature (Crouch,1977). A satisfactory agreement is observed between our results and the published data with the exception of the masses:A=134 and A=140. 1 tab., 2 refs. (author)

  1. Gamma spectrometric validation of measurements test of radionuclides in food matrices

    International Nuclear Information System (INIS)

    Rosa, Mychelle M.L.; Custodio, Luis G.; Bonifacio, Rodrigo L.; Taddei, Maria Helena T.

    2013-01-01

    In a testing laboratory the quality system encompasses a set of activities planned and systematic, which ensure the traceability process of an analysis, which is based on the standards NBR ISO/TEC 17025. With the need for analysis of radionuclides in food products to meet the requirements of import and export, accreditation of testing on this standard becomes increasingly necessary. The Gamma Spectrometry is a technique used for direct determination of radionuclides in different matrices, among them the food, being possible the simultaneous determination of different radionuclides in the same sample without the need for a chemical separation. In the process of Accreditation the methodology validation is an important step that includes testing accuracy, traceability, linearity and recovery. This paper describes the procedures used to validate the assay for determining radionuclides using gamma spectrometry in food. These procedures were performed through analysis of a certificated reference material by the International Atomic Energy Agency (IAEA Soil 327), analysis of samples of milk powder prepared from the doping with certified liquid standards also by the results obtained in the participation of tests of proficiency in analysis of environmental samples. (author)

  2. Application of airborne gamma spectrometric survey data to estimating terrestrial gamma-ray dose rates: An example in California

    International Nuclear Information System (INIS)

    Wollenberg, H.A.; Revzan, K.L.; Smith, A.R.

    1992-01-01

    The authors examine the applicability of radioelement data from the National Aerial Radiometric Reconnaissance (NARR) to estimate terrestrial gamma-ray absorbed dose rates, by comparing dose rates calculated from aeroradiometric surveys of U, Th, and K concentrations in 1 x 2 degree quadrangles with dose rates calculated from a radiogeologic data base and the distribution of lithologies in California. Gamma-ray dose rates increase generally from north to south following lithological trends. Low values of 25--30 nG/h occur in the northernmost quadrangles where low-radioactivity basaltic and ultramafic rocks predominate. Dose rates then increase southward due to the preponderance of clastic sediments and basic volcanics of the Franciscan Formation and Sierran metamorphics in north central and central California, and to increasing exposure southward of the Sierra Nevada batholith, Tertiary marine sedimentary rocks, intermediate to acidic volcanics, and granitic rocks of the Coast Ranges. High values, to 100 nGy/h occur in southeastern California, due primarily to the presence of high-radioactivity Precambrian and pre Cenozoic metamorphic rocks. Lithologic-based estimates of mean dose rates in the quadrangles generally match those from aeroradiometric data, with statewide means of 63 and 60 nGy/h, respectively. These are intermediate between a population-weighted global average of 51 nGy/h and a weighted continental average of 70 nGy/h, based on the global distribution of rock types. The concurrence of lithologically- and aeroradiometrically- determined dose rates in California, with its varied geology and topography encompassing settings representative of the continents, indicates that the NARR data are applicable to estimates of terrestrial absorbed dose rates from natural gamma emitters

  3. Decision Threshold and Detection Limit in Spectrometric Measurements. Part 1: Application to Gamma Spectrometry

    International Nuclear Information System (INIS)

    Perez, C.; Gasco, C.; Lopez, M. A.

    2010-01-01

    This report summarised the author's lecture of the advanced gamma spectrometry course organised by CIEMAT. The characteristic limits determination in gamma spectrometry generally is obtained through the programming that the trade marks offers to the client with the objective of the automatic calculation of the activity concentrations existing in a sample. In this report, the examples shown in the ISO 11929 standard are compared to the programming realised by Genie 2k for determining characteristic limits. The main difference of both is located in the uncertainty calculations due to the efficiency calibration that is considered by ISO and not by Genie 2K. Through implementation in the software developed by trade marks will be possible to introduce this uncertainty and to assimilate to the calculation done by ISO 11929. In the second part of this report will be analyzed the more complicated samples of this application as counting in a whole body counter (following ISO-28218 about Performance Criteria for radio bioassay), multiplet, overlapping, addition of several peaks for obtaining the activity concentration, etc. (Author) 19 refs.

  4. A contribution of airborne magnetic, gamma ray spectrometric data in understanding the structure of the Central Jebilet Hercynian massif and implications for mining

    Science.gov (United States)

    Maacha, Lhou; Jaffal, Mohammed; Jarni, Abdelmajid; Kchikach, Azzouz; Mouguina, El Mostafa; Zouhair, Mohamed; Ennaciri, Aomar; Saddiqi, Omar

    2017-10-01

    The Central Jebilet massif, well-known for its mining potential, has been explored for several years by the Managem Group, in collaboration with the National Office of Hydrocarbons and Mines (ONHYM), Morocco. This massif was surveyed by high-resolution magnetic and gamma-ray spectrometric methods in 1997 as part of a broader exploration program. In order to better exploit the results of this survey in understanding the structure of the Central Jebilet massif, we performed a series of processing of the collected data. The qualitative interpretation of this data highlighted the various magnetic domains, structures (e.g., lineaments and faults), and mafic intrusions. Euler deconvolution calculations provided estimates of the spatial location and depth of the magnetic sources, and spectral analysis of the magnetic data allowed further refinement of these depth estimates. Quantitative interpretation of some anomalies associated with exposed gossans allowed the characterization of their causative bodies, inferred to be sulfide deposits. The magnetic character of both the potential massive-sulfide bodies and the basic magmatic rocks (gabbro) were determined by the aeromagnetic data. Gamma ray spectrometric data has helped facilitate lithological discrimination and alteration zones, based on the radio-elemental distribution in the area. For example, the Thorium to Potassium ratio (Th/K) was used to highlight potassic alteration zones associated with massive-sulfide deposits in the Central Jebilet. The combined magnetic and radiometric study reveals the magnetic character of the Central Jebilet gossans, due to the content of pyrrhotite, which along with potassic alterations, has been recognized in all the known deposits of the Marrakech region. The results of this geophysical campaign supplement the existing geological and structural maps of Central Jebilet massif.

  5. [Determination of trace cobalt in human urine by graphite furnace atomic absorption spectrometr].

    Science.gov (United States)

    Zhong, L X; Ding, B M; Jiang, D; Liu, D Y; Yu, B; Zhu, B L; Ding, L

    2016-05-20

    To establish a method to determine cobalt in human urine by graphite furnace atomic absorption spectrometry. Urine with 2% nitric acid diluted two-fold, to quantify the curve, graphite furnace atomic absorption spectrometric detection. Co was linear within 2.5~40.0 ng/ml with r>0.999. Spike experiment showed that Co received good recovery rate, which was 90.8%~94.8%. Intra-assay precisions were 3.2%~5.1% for Co, inter-assay precisions were 4.4%~5.2% for Co. The method by using graphite furnace atomic absorption spectrometr to determine urine Co was fast, accurate and with low matrix effect. It could meet the requirement in GBZ/T 210.5-2008.

  6. Gamma spectrometric measurements of power distribution and burnup on irradiated fuel elements of light water reactors

    International Nuclear Information System (INIS)

    Bouchard, Jacques; Frejaville, Gerard; Robin, Michel.

    1977-08-01

    Based on experience gained from experiments at the COMIR laboratory and with the installation at the Adennes reactor and on the use of these results for evaluation of calculation methods, this report includes a synthesis of the aspects concerning in particular non-destructive measurement of irradiated fuel in water reactors, fuel assemblies or fuel pins. Following a brief summary of gamma emitting radioactive fission products and, measurement conditions, there is a description of the fuel cooling installation at the Ardennes reactor, including the results obtained with this installation as well as from measurements on the fuel pins. In conclusion, the problem concerning burn-up determination, especially the 134 Cs/ 137 Cs method, are discussed [fr

  7. Uranium determination using atomic spectrometric techniques: An overview

    International Nuclear Information System (INIS)

    Santos, Juracir S.; Teixeira, Leonardo S.G.; Santos, Walter N.L. dos; Lemos, Valfredo A.; Godoy, Jose M.; Ferreira, Sergio L.C.

    2010-01-01

    This review focuses on the determination of uranium using spectroanalytical techniques that are aimed at total determination such as flame atomic absorption spectrometry (FAAS), electrothermal atomic absorption spectrometry (ETAAS), inductively coupled plasma optical emission spectrometry (ICP-OES); and inductively coupled plasma mass spectrometry (ICP-MS) that also enables the determination of uranium isotopes. The advantages and shortcomings related to interferences, precision, accuracy, sample type and equipment employed in the analysis are taken into account, as well as the complexity and costs (i.e., acquisition, operation and maintenance) associated with each of the techniques. Strategies to improve their performance that employ separation and/or preconcentration steps are considered, with an emphasis given to solid-phase extraction because of its advantages compared to other preconcentration procedures.

  8. Rapid gamma spectrometric analysis of soil samples after radioactive fallout using a "conjugate view" technique.

    Science.gov (United States)

    Isaksson, M; Fahlström, M; Ossipova, N; Rosén, K

    2017-10-01

    A method for fast determination of the activity in soil samples by measuring a fresh soil core sample from both ends with an HPGe-detector is proposed. The method was tested by simulations, as well as by measurements on spiked soil samples. Both simulations and measurements showed that the geometrical mean of the count rates when the sample is measured twice, with the bottom and the top end, respectively, facing the detector closely resembles the count rate from a measurement on a homogenized sample. Therefore, an efficiency calibration for homogenized samples could be used even if the activity is highly inhomogeneous in the soil core, as is the case with fresh fallout. It was also shown that by studying the ratio between the two measurements, a rough estimation of the extent of penetration of the radionuclide in the soil can be found. This will enhance the possibility to make rapid estimations of the soil inventory by field gamma spectrometry. Copyright © 2017 Elsevier Ltd. All rights reserved.

  9. Analysis of cows' milk in the content of radioactive cs137 gamma-spectrometric method

    International Nuclear Information System (INIS)

    Zagidulin, Z.Z.; Isayev, R.Sh.; Guseynova, I.A.

    2010-01-01

    Full text : The most intense pollution of the environment Cs137 (after the ban of atmospheric nuclear weapons tests), was the result of the Chernobyl accident in 1986. The consequence of this accident was the accumulation of large amounts of Cs-137 in the atmosphere, which was the source of the global fallout of this isotope in the Earth's surface, including the territory of Azerbaijan. When considering livestock as one of the links of contamination by radioactive substances in food chains should be recognized that the main risk associated with the accumulation of radioactive Cs137 in the soil, plants and animal products originating ultimately in the human diet. The aim of this study was to determine the radioactive Cs137 in cow's milk. Subsequent samples of milk were purchased in stores and have been measured in the native form. Pal Sud milk produced in Azerbaijan. On Health - Russia. Savushkin product - Belarus. As a radiometric measurement setup Cs137 in cow's milk was used semiconductor gamma-ray spectrometer with a detection unit based on the detection of high-purity germanium (manufactured by Canberra) in the lead shielding.

  10. Automation of a gamma spectrometric analysis method for naturally occuring radionuclides in different materials (NORM)

    International Nuclear Information System (INIS)

    Marzocchi, Olaf

    2009-06-01

    This work presents an improvement over the standard analysis routine used in the Physikalisches Messlabor to detect gamma peaks in spectra from naturally occurring radioactive materials (NORM). The new routine introduces the use of custom libraries of known gamma peaks, in order to ease the work of the software than can therefore detect more peaks. As final result, the user performing the analysis has less chances of making errors and can also analyse more spectra in the same amount of time. A new software, with an optimised interface able to further enhance the productivity of the user, is developed and validated. (orig.)

  11. Fully Automated Spectrometric Protocols for Determination of Antioxidant Activity: Advantages and Disadvantages

    Directory of Open Access Journals (Sweden)

    Marketa Ryvolova

    2010-11-01

    Full Text Available The aim of this study was to describe behaviour, kinetics, time courses and limitations of the six different fully automated spectrometric methods - DPPH, TEAC, FRAP, DMPD, Free Radicals and Blue CrO5. Absorption curves were measured and absorbance maxima were found. All methods were calibrated using the standard compounds Trolox® and/or gallic acid. Calibration curves were determined (relative standard deviation was within the range from 1.5 to 2.5 %. The obtained characteristics were compared and discussed. Moreover, the data obtained were applied to optimize and to automate all mentioned protocols. Automatic analyzer allowed us to analyse simultaneously larger set of samples, to decrease the measurement time, to eliminate the errors and to provide data of higher quality in comparison to manual analysis. The total time of analysis for one sample was decreased to 10 min for all six methods. In contrary, the total time of manual spectrometric determination was approximately 120 min. The obtained data provided good correlations between studied methods (R = 0.97 – 0.99.

  12. Reduction of beta-interference in gamma-spectrometric measurements of neutron-irradiated geological material

    International Nuclear Information System (INIS)

    Garmann, L.B.

    1986-01-01

    The analytical technique for INAA, when applied to geological materials, is improved by introducing an electromagnetic field between sample and detector. This field lowers the bremsstrahlung background intensity in the gamma-spectrum by reducing the number of beta-particles reaching the detector. Thus precision, accuracy and lower detection limit are improved. The technique was used on alkalisyenite and on meteoritic material, rocks containing high quantities of sodium and iron, respectively. After neutron irradiation, the induced nuclides sup(24)Na and sup(59)Fe are responsible for high bremsstrahlung interference, which under normal analyitical conditions would mask any x-ray or gamma-ray peaks of interest. The technique is easily applied to multielement analysis of geological and biological materials. It can be combined with sophisticated spectrum-treating techniques such as spectrum stripping and spectrum smoothing, or coincidence-anticoincidence circuits. (author)

  13. Determination of plutonium-241 half-life by mass spectrometric measurement

    International Nuclear Information System (INIS)

    Hiyama, Takashi; Wada, Yukio; Onishi, Koichi

    1982-01-01

    Much data for Pu-241 half-life have been reported, but these values range from 13.8 years to 15.1 years depending on investigators. In order to define the half-life of Pu-241, the half-life was calculated by analyzing the mass spectrometry data obtained in the author's laboratory over the past six years on Plutonium Isotopic Standard Reference Materials prepared at the National Bureau of Standards (NBS). The sample used for this work consisted of SRM-947 and SRM-948 prepared at NBS. Before mass spectrometric analysis, the plutonium aliquot was separated from its Am-241 daughter by anion exchange chromatography, since Am-241 is not distinguished from Pu-241 in the mass spectrometer. 241 Pu/ 239 Pu and 241 Pu/ 240 Pu ratios were calculated from the values of mass spectrometric measurement. From the relation of log N to time, the half-life of Pu-241 was determined, based on the slope using a least squares fit. The half-life of Pu-241 was estimated to be 14.29+-0.15 years. (Yoshitake, I.)

  14. Spectrometric gamma investigations concerning zinc-lead ores and the products of their processing

    International Nuclear Information System (INIS)

    Girczys, J.; Skowronek, J.; Zrodlowski, B.

    1983-01-01

    Zinc-lead ore and products of its enrichment were investigated using gamma spectrometry for the content of uranium, thorium and potassium 40. It was stated that the mean content of these elements in a deposit does not diverge from their mean concentration in the lithosphere. They also accompany the surrounding rocks. As a result of mechanical processing of this ore radionuclides pass discards in which they do not form concentrations dangerous for life, either. In the exploitation areas and in the surroundings there is no state of ecological hazard. (author)

  15. Determination of the $e^+ e^- \\to \\gamma \\gamma (\\gamma)$ cross-section at LEP 2

    CERN Document Server

    Abdallah, J; Adam, W; Adzic, P; Albrecht, T; Alderweireld, T; Alemany-Fernandez, R; Allmendinger, T; Allport, P P; Amaldi, Ugo; Amapane, N; Amato, S; Anashkin, E; Andreazza, A; Andringa, S; Anjos, N; Antilogus, P; Apel, W D; Arnoud, Y; Ask, S; Åsman, B; Augustin, J E; Augustinus, A; Baillon, Paul; Ballestrero, A; Bambade, P; Barbier, R; Bardin, Dimitri Yuri; Barker, G J; Baroncelli, A; Battaglia, Marco; Baubillier, M; Becks, K H; Begalli, M; Behrmann, A; Ben-Haim, E; Benekos, N C; Benvenuti, Alberto C; Bérat, C; Berggren, M; Berntzon, L; Bertrand, D; Besançon, M; Besson, N; Bloch, D; Blom, M; Bluj, M; Bonesini, M; Boonekamp, M; Booth, P S L; Borisov, G; Botner, O; Bouquet, B; Bowcock, T J V; Boyko, I; Bracko, M; Brenner, R; Brodet, E; Brückman, P; Brunet, J M; Bugge, L; Buschmann, P; Calvi, M; Camporesi, T; Canale, V; Carena, F; Castro, N; Cavallo, F R; Chapkin, M M; Charpentier, P; Checchia, P; Chierici, R; Shlyapnikov, P; Chudoba, J; Chung, S U; Cieslik, K; Collins, P; Contri, R; Cosme, G; Cossutti, F; Costa, M J; Crennell, D J; Cuevas-Maestro, J; D'Hondt, J; Dalmau, J; Da Silva, T; Da Silva, W; Della Ricca, G; De Angelis, A; de Boer, Wim; De Clercq, C; De Lotto, B; De Maria, N; De Min, A; De Paula, L S; Di Ciaccio, L; Di Simone, A; Doroba, K; Drees, J; Dris, M; Eigen, G; Ekelöf, T J C; Ellert, M; Elsing, M; Espirito-Santo, M C; Fanourakis, G K; Fassouliotis, D; Feindt, M; Fernández, J; Ferrer, A; Ferro, F; Flagmeyer, U; Föth, H; Fokitis, E; Fulda-Quenzer, F; Fuster, J A; Gandelman, M; García, C; Gavillet, P; Gazis, E N; Gokieli, R; Golob, B; Gómez-Ceballos, G; Gonçalves, P; Graziani, E; Grosdidier, G; Grzelak, K; Guy, J; Haag, C; Hallgren, A; Hamacher, K; Hamilton, K; Haug, S; Hauler, F; Hedberg, V; Hennecke, M; Herr, H; Hoffman, J; Holmgren, S O; Holt, P J; Houlden, M A; Hultqvist, K; Jackson, J N; Jarlskog, G; Jarry, P; Jeans, D; Johansson, E K; Johansson, P D; Jonsson, P; Joram, C; Jungermann, L; Kapusta, F; Katsanevas, S; Katsoufis, E C; Kernel, G; Kersevan, B P; Kerzel, U; Kiiskinen, A P; King, B T; Kjaer, N J; Kluit, P; Kokkinias, P; Kourkoumelis, C; Kuznetsov, O; Krumshtein, Z; Kucharczyk, M; Lamsa, J; Leder, G; Ledroit, F; Leinonen, L; Leitner, R; Lemonne, J; Lepeltier, V; Lesiak, T; Liebig, W; Liko, D; Lipniacka, A; Lopes, J H; López, J M; Loukas, D; Lutz, P; Lyons, L; MacNaughton, J; Malek, A; Maltezos, S; Mandl, F; Marco, J; Marco, R; Maréchal, B; Margoni, M; Marin, J C; Mariotti, C; Markou, A; Martínez-Rivero, C; Masik, J; Mastroyiannopoulos, N; Matorras, F; Matteuzzi, C; Mazzucato, F; Mazzucato, M; McNulty, R; Meroni, C; Migliore, E; Mitaroff, W A; Mjörnmark, U; Moa, T; Moch, M; Mönig, K; Monge, R; Montenegro, J; Moraes, D; Moreno, S; Morettini, P; Müller, U; Münich, K; Mulders, M; Mundim, L; Murray, W; Muryn, B; Myatt, G; Myklebust, T; Nassiakou, M; Navarria, Francesco Luigi; Nawrocki, K; Nicolaidou, R; Nikolenko, M; Oblakowska-Mucha, A; Obraztsov, V F; Olshevskii, A G; Onofre, A; Orava, R; Österberg, K; Ouraou, A; Oyanguren, A; Paganoni, M; Paiano, S; Palacios, J P; Palka, H; Papadopoulou, T D; Pape, L; Parkes, C; Parodi, F; Parzefall, U; Passeri, A; Passon, O; Peralta, L; Perepelitsa, V F; Perrotta, A; Petrolini, A; Piedra, J; Pieri, L; Pierre, F; Pimenta, M; Piotto, E; Podobnik, T; Poireau, V; Pol, M E; Polok, G; Pozdnyakov, V; Pukhaeva, N; Pullia, Antonio; Rames, J; Read, A; Rebecchi, P; Rehn, J; Reid, D; Reinhardt, R; Renton, P B; Richard, F; Rídky, J; Rivero, M; Rodríguez, D; Romero, A; Ronchese, P; Roudeau, P; Rovelli, T; Ruhlmann-Kleider, V; Ryabtchikov, D; Sadovskii, A; Salmi, L; Salt, J; Sander, C; Savoy-Navarro, A; Schwickerath, U; Segar, A; Sekulin, R L; Siebel, M; Sissakian, A N; Smadja, G; Smirnova, O G; Sokolov, A; Sopczak, A; Sosnowski, R; Spassoff, Tz; Stanitzki, M; Stocchi, A; Strauss, J; Stugu, B; Szczekowski, M; Szeptycka, M; Szumlak, T; Tabarelli de Fatis, T; Taffard, A C; Tegenfeldt, F; Timmermans, J; Tkatchev, L G; Tobin, M; Todorovova, S; Tomé, B; Tonazzo, A; Tortosa, P; Travnicek, P; Treille, D; Tristram, G; Trochimczuk, M; Troncon, C; Turluer, M L; Tyapkin, I A; Tyapkin, P; Tzamarias, S; Uvarov, V; Valenti, G; van Dam, P; Van Eldik, J; Van Lysebetten, A; Van Remortel, N; Van Vulpen, I; Vegni, G; Veloso, F; Venus, W A; Verdier, P; Verzi, V; Vilanova, D; Vitale, L; Vrba, V; Wahlen, H; Washbrook, A J; Weiser, C; Wicke, D; Wickens, J H; Wilkinson, G; Winter, M; Witek, M; Yushchenko, O P; Zalewska-Bak, A; Zalewski, P; Zavrtanik, D; Zhuravlov, V; Zimin, N I; Zintchenko, A; Zupan, M

    2004-01-01

    A test of the benchmark QED process e+e- -> gamma gamma (gamma) is reported, using the data collected with the DELPHI detector at LEP 2. The data analysed were recorded at centre-of-mass energies ranging from 161 GeV to 208 GeV and correspond to a total integrated luminosity of 656.4 pb^{-1}. The Born cross-section for the process e+e- -> gamma gamma (gamma) was determined, confirming the validity of QED at the highest energies ever attained in electron-positron collisions. Lower limits on the parameters of a number of possible deviations from QED, predicted within theoretical frameworks expressing physics beyond the Standard Model, were derived.

  16. Separation Techniques for Uranium and Plutonium at Trace Levels for the Thermal Ionization Mass Spectrometric Determination

    Energy Technology Data Exchange (ETDEWEB)

    Suh, M. Y.; Han, S. H.; Kim, J. G.; Park, Y. J.; Kim, W. H

    2005-12-15

    This report describes the state of the art and the progress of the chemical separation and purification techniques required for the thermal ionization mass spectrometric determination of uranium and plutonium in environmental samples at trace or ultratrace levels. Various techniques, such as precipitation, solvent extraction, extraction chromatography, and ion exchange chromatography, for separation of uranium and plutonium were evaluated. Sample preparation methods and dissolution techniques for environmental samples were also discussed. Especially, both extraction chromatographic and anion exchange chromatographic procedures for uranium and plutonium in environmental samples, such as soil, sediment, plant, seawater, urine, and bone ash were reviewed in detail in order to propose some suitable methods for the separation and purification of uranium and plutonium from the safeguards environmental or swipe samples. A survey of the IAEA strengthened safeguards system, the clean room facility of IAEA's NWAL(Network of Analytical Laboratories), and the analytical techniques for safeguards environmental samples was also discussed here.

  17. Separation Techniques for Uranium and Plutonium at Trace Levels for the Thermal Ionization Mass Spectrometric Determination

    International Nuclear Information System (INIS)

    Suh, M. Y.; Han, S. H.; Kim, J. G.; Park, Y. J.; Kim, W. H.

    2005-12-01

    This report describes the state of the art and the progress of the chemical separation and purification techniques required for the thermal ionization mass spectrometric determination of uranium and plutonium in environmental samples at trace or ultratrace levels. Various techniques, such as precipitation, solvent extraction, extraction chromatography, and ion exchange chromatography, for separation of uranium and plutonium were evaluated. Sample preparation methods and dissolution techniques for environmental samples were also discussed. Especially, both extraction chromatographic and anion exchange chromatographic procedures for uranium and plutonium in environmental samples, such as soil, sediment, plant, seawater, urine, and bone ash were reviewed in detail in order to propose some suitable methods for the separation and purification of uranium and plutonium from the safeguards environmental or swipe samples. A survey of the IAEA strengthened safeguards system, the clean room facility of IAEA's NWAL(Network of Analytical Laboratories), and the analytical techniques for safeguards environmental samples was also discussed here

  18. Determination of isotope fractionation effect using a double spike (242Pu+240Pu) during the mass spectrometric analysis of plutonium

    International Nuclear Information System (INIS)

    Chitambar, S.A.; Parab, A.R.; Khodade, P.S.; Jain, H.C.

    1986-01-01

    Isotope fractionation effect during the mass spectrometric analysis of plutonium has been investigated using a double spike ( 242 Pu+ 240 Pu) and the determination of concentration of plutonium in dissolver solution of irradiated fuel is reported. (author). 6 refs., 2 tables

  19. Burn-Up Determination by High Resolution Gamma Spectrometry: Axial and Diametral Scanning Experiments

    Energy Technology Data Exchange (ETDEWEB)

    Forsyth, R.S.; Blackadder, W.H.; Ronqvist, N.

    1967-02-15

    In the gamma spectrometric determination of burn-up the use of a single fission product as a monitor of the specimen fission rate is subject to errors caused by activity saturation or, in certain cases, fission product migration. Results are presented of experiments in which all the resolvable gamma peaks in the fission product spectrum have been used to calculate the fission rate; these results form a pattern which reflect errors in the literature values of the gamma branching ratios, fission yields etc., and also represent a series of empirical correction factors. Axial and diametral scanning experiments on a long-irradiated low-enrichment fuel element are also described and demonstrate that it is possible to differentiate between fissions in U-235 and in Pu-239 respectively by means of the ratios of the Ru-106 activity to the activities of the other fission products.

  20. Gamma-spectrometric surveys in differentiated granites. I: a review of the method and of the geochemical behavior of K, Th and U

    International Nuclear Information System (INIS)

    Ulbrich, Horstpeter Herberto Gustavo Jose; Ulbrich, Mabel Norma Costas; Guimaraes, Gilson Burigo

    2009-01-01

    This contribution is part of a research project on the Neo proterozoic Cunhaporanga Granitic Complex (CGC), cropping out in the Ponta Grossa Arch (Parana state, SE Brazil). An initial study used the gamma-spectrometric data of the Serra do Mar Sul Aero geophysical Project, performed during the 70's for CPRM. Later, terrestrial gamma-spectrometric surveys focused on the study of the differentiated Joaquim Murtinho Granite (JMG) in the NW corner of CGC, and the Serra do Carambei Granite, to the SW. In this paper, the results obtained for JMG are presented in two parts. The first deals with methodology and the presentation of several gamma-spectrometric 'color-scale' maps, indicating that results obtained in granites depend strongly on a climatic factor, given the mobility of K during weathering in subtropical climates with strong rainfalls, also favoring a greater mobility of U. Minerals that are U and Th hosts, documented in granites, are reviewed, together with the weathering processes that control the mobility of K, U and Th in soils. Strong K signals in granitic areas submitted to these climates document the presence of fresh rock and/or effects of hydrothermal alteration, while weak or nil signals are evidence of strong leaching of K during weathering. U and Th will be retained in the residual soils, in part leading to their selective enrichment, also coupled with soil migration to lower topographic levels by colluvial transport. The larger solubility of U (as uranyl ion) allows its liberation under oxidizing conditions, and its migration, limited by the possibility of absorption in newly formed mineral and organic soil phases. Th should be retained almost totally in resistant phases and, when liberated in solution, will mostly be fixed in organic and inorganic soil substances. (author)

  1. Review of procedures involving separation and preconcentration for the determination of cadmium using spectrometric techniques

    International Nuclear Information System (INIS)

    Ferreira, Sergio L.C.; Andrade, Jailson B. de; Korn, Maria das Gracas A.; Pereira, Madson de G.; Lemos, Valfredo A.; Santos, Walter N.L. dos; Rodrigues, Frederico de Medeiros; Souza, Anderson S.; Ferreira, Hadla S.; Silva, Erik G.P. da

    2007-01-01

    Spectrometric techniques for the analysis of trace cadmium have developed rapidly due to the increasing need for accurate measurements at extremely low levels of this element in diverse matrices. This review covers separation and preconcentration procedures, such as electrochemical deposition, precipitation, coprecipitation, solid phase extraction, liquid-liquid extraction (LLE) and cloud point extraction (CPE), and consider the features of the their application with several spectrometric techniques

  2. Precise timing of the last interglacial period from mass spectrometric determination of thorium-230 in corals

    Science.gov (United States)

    Chen, J. H.; Wasserburg, G. J.; Ku, T.-L.; Edwards, R. Lawrence

    1987-01-01

    The development of mass spectrometric techniques for determination of Th-230 abundance has made it possible to reduce analytical errors in (U-238)-(U-234)-(Th-230) dating of corals even with very small samples. Samples of 6 x 10 to the 8th atoms of Th-230 can be measured to an accuracy of + or - 3 percent (2sigma), and 3 x 10 to the 10th atoms of Th-230 can be measured to an accuracy of + or - 0.2 percent. The time range over which useful age data on corals can be obtained now ranges from about 50 to about 500,000 years. For young corals, this approach may be preferable to C-14 dating. The precision with which the age of a coral can now be determined should make it possible to critically test the Milankovitch hypothesis concerning Pleistocene climate fluctuations. Analyses of a number of corals that grew during the last interglacial period yield ages of 122,000 to 130,000 years. The ages coincide with, or slightly post-date, the summer solar insolation high at 65 deg N latitude which occurred 128,000 years ago. This supports the idea that changes in Pleistocene climate can be the result of variations in the distribution of solar insolation caused by changes in the geometry of the earth's orbit and rotation axis.

  3. Determination of platinum originated from antitumoral drugs in human urine by atomic absorption spectrometric methods.

    Science.gov (United States)

    da Costa, Anilton Coelho; Vieira, Mariana Antunes; Luna, Aderval Severino; de Campos, Reinaldo Calixto

    2010-10-15

    Cisplatin and carboplatin are the most common platinum-based drugs used in cancer treatment. Pharmacokinetic investigations, the evaluation of the body burden during the treatment, as well as baseline levels of platinum in humans have attracted great interest. Thus, accurate analytical methods for fast and easy Pt monitoring in clinical samples become necessary. In the present study atomic absorption spectrometric methods for the determination of platinum in the forms of cisplatin and carboplatin in human urine were investigated. Platinum, in these different forms, could be determined in urine, after simple sample dilution. Regarding electrothermal atomic absorption spectrometry, the optimum parameters were defined by a central composite design optimization. Multiplicative matrix effects were overcome by using a mixture of HCl and NaCl as modifier. The limit of detection (LOD) was 0.004 mgL(-1) of platinum in the original sample. For the analysis of more concentrated samples, high resolution continuous source flame atomic absorption spectrometry was also investigated. Flame conditions were optimized by a multivariate D-optimal design, using as response the sum of the analyte addition calibration slopes and their standard deviations. Matrix matched external calibration with PtCl(2) calibration solutions, was possible, and the LOD was 0.06 mgL(-1) in the original sample. The results obtained by the proposed procedures were also in good agreement with those obtained by an independent comparative procedure. Copyright © 2010 Elsevier B.V. All rights reserved.

  4. Column preconcentration and electrothermal atomic absorption spectrometric determination of rhodium in some food and standard samples.

    Science.gov (United States)

    Taher, Mohammad Ali; Pourmohammad, Fatemeh; Fazelirad, Hamid

    2015-12-01

    In the present work, an electrothermal atomic absorption spectrometric method has been developed for the determination of ultra-trace amounts of rhodium after adsorption of its 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol/tetraphenylborate ion associated complex at the surface of alumina. Several factors affecting the extraction efficiency such as the pH, type of eluent, sample and eluent flow rates, sorption capacity of alumina and sample volume were investigated and optimized. The relative standard deviation for eight measurements of 0.1 ng/mL of rhodium was ±6.3%. In this method, the detection limit was 0.003 ng/mL in the original solution. The sorption capacity of alumina and the linear range for Rh(III) were evaluated as 0.8 mg/g and 0.015-0.45 ng/mL in the original solution, respectively. The proposed method was successfully applied for the extraction and determination of rhodium content in some food and standard samples with high recovery values. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Determination of ractopamine in pig hair using liquid chromatography with tandem mass spectrometric detection.

    Science.gov (United States)

    Wu, Junlin; Liu, Xiaoyun; Peng, Yunping

    2014-01-01

    A quantitative analytical procedure for the determination of ractopamine in pig hair has been developed and validated. The hair samples were washed and incubated at 75°C with isoxuprine and hair extraction buffer. The drug present was quantified using mixed solid-phase extraction and liquid chromatography with tandem mass spectrometric detection. The limit of quantization (LOQ) was 10pg/mg and the intra-day precision at 25pg/mg and 750pg/mg was 0.49% and 2.8% respectively. Inter-day precision was 0.88% and 3.52% at the same concentrations. The hair extraction percentage recovery at 25pg/mg and 50ng/mL was 99.47% and 103.83% respectively. The extraction percentage recovery at 25pg/mg and 50ng/mg was 93.52% and 100.26% respectively. Our results showed that ractopamine residues persist in hair in 24days of withdrawal and also showed the possibility to test ractopamine from pig hair samples. Copyright © 2014 Elsevier Inc. All rights reserved.

  6. Electrospray ionization mass spectrometric analysis of newly synthesized alpha,beta-unsaturated gamma-lactones fused to sugars.

    Science.gov (United States)

    Madeira, Paulo J Amorim; Rosa, Ana Margarida; Xavier, Nuno M; Rauter, Amélia P; Florêncio, M Helena

    2010-04-15

    Knowledge of the fragmentation mechanisms of lactones and their behaviour under electrospray ionization (ESI) conditions can be extended to larger and more complex natural products that contain an alpha,beta-unsaturated gamma-lactone moiety in their structure. Moreover, little is known about the gas-phase behaviour of alpha,beta-unsaturated gamma-lactones linked or fused to sugars. Therefore, five alpha,beta-unsaturated gamma-lactones (butenolides) fused to a pyranose ring, recently synthesized compounds with potential relevance regarding their biological properties, were investigated using ESI-MS and ESI-MS/MS in both positive and negative ion modes. Their fragmentation mechanisms and product ion structures were compared. It was observed that two isomers could be unambiguously distinguished in the negative ion mode by the fragmentation pathways of their deprotonated molecules as well as in the positive ion mode by the fragmentation pathways of either the protonated or the sodiated molecule. Fragmentation mechanisms are proposed taking into account the MS/MS data and semi-empirical calculations using the PM6 Hamiltonean. The semi-empirical calculations were also very useful in determining the most probable protonation and cationization sites. 2010 John Wiley & Sons, Ltd.

  7. Determination of the hydraulic conductivity in column of undeformed soil by gamma rays transmission

    International Nuclear Information System (INIS)

    Moreira, Anderson C.; Cavalcante, Fabio H.M.; Portezan Filho, Otavio; Coimbra, Melayne M.; Appoloni, Carlos Roberto

    2000-01-01

    The water infiltration process in undeformed soil column and the measurement of redistribution process by gamma rays transmission in different depth allow the determination of Hydraulic Conductivity K(Θ) function, using the Sisson et al. (1980) method. A LRd (dystrophic dark red soil) soil column with 60 cm of height, 10 cm of width and 5 cm of thickness, was analyzed in laboratory, reproducing the field conditions concerning to the water infiltration and redistribution in the soil. The soil moisture content data was obtained with a radioactivity source 241 Am (100 mCi; 59,6 keV), NaI (Tl) 2x2 detector, coupled to an gamma rays spectrometric electronic chain and a measurement table that allowed the vertical displacement of the soil column. The results indicate a growing behavior for K(Θ) in relation to the depth. The collimators had 2 mm and 5 mm diameter for radioactivity source and detector respectively. (author)

  8. Comparison of accelerator mass spectrometric measurement with liquid scintillation counting measurement for the determination of 14C in environmental samples

    International Nuclear Information System (INIS)

    Yasuike, Kaeko; Yamada, Yoshimune; Amano, Hikaru

    2010-01-01

    The concentrations of organically-bound 14 C in tree-ring cellulose of a Japanese Black Pine grown in Shika-machi (37.0 deg. N, 136.8 deg. E) and those of a Japanese Cedar grown in Kanazawa (36.5 deg. N, 136.7 deg. E), Japan, were analyzed for the ring-years from 1989 to 1998 by the accelerator mass spectrometric measurement. The results were compared with those of the same samples analyzed by the liquid scintillation counting measurement to determine the reliability of liquid scintillation counting measurement. An important result of this study is that the sensitivity and reproducibility of accelerator mass spectrometric measurement was almost equal to that of liquid scintillation counting measurement.

  9. Continuous flow hydride generation-atomic fluorescence spectrometric determination and speciation of arsenic in wine

    Energy Technology Data Exchange (ETDEWEB)

    Karadjova, Irina B. [Faculty of Chemistry, University of Sofia, 1 James Bourchier Blvd., Sofia 1164 (Bulgaria); Lampugnani, Leonardo [C.N.R. Istituto per i processi chimico-fisici, Area della Ricerca di Pisa, Via Moruzzi 1, 56124 Pisa (Italy)]. E-mail: lampugnani@ipcf.cnr.it; Onor, Massimo [C.N.R. Istituto per i processi chimico-fisici, Area della Ricerca di Pisa, Via Moruzzi 1, 56124 Pisa (Italy); D' Ulivo, Alessandro [C.N.R. Istituto per i processi chimico-fisici, Area della Ricerca di Pisa, Via Moruzzi 1, 56124 Pisa (Italy); Tsalev, Dimiter L. [Faculty of Chemistry, University of Sofia, 1 James Bourchier Blvd., Sofia 1164 (Bulgaria)

    2005-07-15

    Methods for the atomic fluorescence spectrometric (AFS) determination of total arsenic and arsenic species in wines based on continuous flow hydride generation (HG) with atomization in miniature diffusion flame (MDF) are described. For hydride-forming arsenic, L-cysteine is used as reagent for pre-reduction and complexation of arsenite, arsenate, monomethylarsonate and dimethylarsinate. Concentrations of hydrochloric acid and tetrahydroborate are optimized in order to minimize interference by ethanol. Procedure permits determination of the sum of these four species in 5-10-fold diluted samples with limit of detection (LOD) 0.3 and 0.6 {mu}g l{sup -1} As in white and red wines, respectively, with precision between 2% and 8% RSD at As levels within 0.5-10 {mu}g l{sup -1}. Selective arsine generation from different reaction media is used for non-chromatographic determination of arsenic species in wines: citrate buffer at pH 5.1 for As(III); 0.2 mol l{sup -1} acetic acid for arsenite + dimethylarsinate (DMA); 8 mol l{sup -1} HCl for total inorganic arsenic [As(III) + As(V)]; and monomethylarsonate (MMA) calculated by difference. Calibration with aqueous and ethanol-matched standard solutions of As(III) is used for 10- and 5-fold diluted samples, respectively. The LODs are 0.4 {mu}g l{sup -1} for As(III) and 0.3 {mu}g l{sup -1} for the other three As species and precision is within 4-8% RSDs. Arsenic species in wine were also determined by coupling of ion chromatographic separation on an anion exchange column and HG-flame AFS detection. Methods were validated by means of recovery studies and comparative analyses by HG-AFS and electrothermal atomic absorption spectrometry after microwave digestion. The LODs were 0.12, 0.27, 0.15 and 0.13 {mu}g l{sup -1} (as As) and RSDs were 2-6%, 5-9%, 3-7% and 2-5% for As(III), As(V), MMA and DMA arsenic species, respectively. Bottled red and white wines from Bulgaria, Republic of Macedonia and Italy were analyzed by non

  10. Utilization of airborne gamma ray spectrometric data for radioactive mineral exploration of G.Abu Had – G.Umm Qaraf area, South Eastern Desert, Egypt

    Directory of Open Access Journals (Sweden)

    A.A. Elkhadragy

    2017-06-01

    Full Text Available Airborne gamma-ray spectrometry method is a powerful tool for geological mapping, mineral exploration and environmental monitoring. Qualitative and quantitative interpretations were performed on the airborne spectrometric data of G.Abu Had – G.Umm Qaraf area, South Eastern Desert, Egypt. Special attention is focused in this paper to discuss the distribution of k, eTh, eU and TC maps. Also there are statistical analyses for the radioactive content for the rock units of the studied area. Anomalies of high radioactive content were calculated and studied by field ground follow-up. The younger granites, Natach volcanic, gneissose granites and pegmatite rocks are the highly content of uranium in the studied area.

  11. Partial vapor-phase hydrolysis of peptide bonds: A method for mass spectrometric determination of O-glycosylated sites in glycopeptides

    DEFF Research Database (Denmark)

    Mirgorodskaya, E; Hassan, H; Wandall, H H

    1999-01-01

    In this study we present a method for determination of O-glycosylation sites in glycopeptides, based on partial vapor-phase acid hydrolysis in combination with mass spectrometric analysis. Pentafluoropropionic acid and hydrochloric acid were used for the hydrolysis of glycosylated peptides....... The reaction conditions were optimized for efficient polypeptide backbone cleavages with minimal cleavage of glycosidic bonds. The glycosylated residues were identified by mass spectrometric analysis of the hydrolytic cleavage products. Although glycosidic bonds are partially cleaved under acid hydrolysis...

  12. Carbon nanotubes as solid-phase extraction sorbents prior to atomic spectrometric determination of metal species: A review

    Energy Technology Data Exchange (ETDEWEB)

    Herrero Latorre, C., E-mail: carlos.herrero@usc.es [Universidad de Santiago de Compostela, Dpto. Quimica Analitica, Nutricion y Bromatologia, Facultad de Ciencias, Alfonso X el Sabio s/n, 27002 Lugo (Spain); Alvarez Mendez, J.; Barciela Garcia, J.; Garcia Martin, S.; Pena Crecente, R.M. [Universidad de Santiago de Compostela, Dpto. Quimica Analitica, Nutricion y Bromatologia, Facultad de Ciencias, Alfonso X el Sabio s/n, 27002 Lugo (Spain)

    2012-10-24

    Highlights: Black-Right-Pointing-Pointer The use of CNTs as sorbent for metal species in solid phase extraction has been described. Black-Right-Pointing-Pointer Physical and chemical strategies for functionalization of carbon nanotubes have been discussed. Black-Right-Pointing-Pointer Published analytical methods concerning solid phase extraction and atomic spectrometric determination have been reviewed. - Abstract: New materials have significant impact on the development of new methods and instrumentation for chemical analysis. From the discovery of carbon nanotubes in 1991, single and multi-walled carbon nanotubes - due to their high adsorption and desorption capacities - have been employed as sorption substrates in solid-phase extraction for the preconcentration of metal species from diverse matrices. Looking for successive improvements in sensitivity and selectivity, in the past few years, carbon nanotubes have been utilized as sorbents for solid phase extraction in three different ways: like as-grown, oxidized and functionalized nanotubes. In the present paper, an overview of the recent trends in the use of carbon nanotubes for solid phase extraction of metal species in environmental, biological and food samples is presented. The determination procedures involved the adsorption of metals on the nanotube surface, their quantitative desorption and subsequent measurement by means of atomic spectrometric techniques such as flame atomic absorption spectrometry, electrothermal atomic absorption spectrometry or inductively coupled plasma atomic emission spectrometry/mass spectrometry, among others. Synthesis, purification and types of carbon nanotubes, as well as the diverse chemical and physical strategies for their functionalization are described. Based on 140 references, the performance and general properties of the applications of solid phase extraction based on carbon nanotubes for metal species atomic spectrometric determination are discussed.

  13. Measurement of 226Ra, 232Th and 40K radioactivity contents in by-product phosphogypsum from phosphate fertilizer industry using gamma ray spectrometric method

    International Nuclear Information System (INIS)

    Demirel, H.; Parmaksiz, A.; Vural, M.; Cakir, I.T.; Demircioglu, B.; Yucel, H.

    2004-01-01

    Full text: Phosphatic fertilizers are produced from the industrial processing of rock phosphate ores which are known to contain naturally occurring radionuclides such as 238 U and its daughter products. A high volume by-product known as phosphogypsum (PG) from the production of phosphoric acid and phosphate fertilizer causes serious storage and environmental problems in phosphoric acid industries. During the phosphoric acid production process, 226 Ra (t 1/2 =1600 y) ends up in PG which has chemical analogous to calcium element. Since the stockpiles of PG near the phosphatic fertilizer plants are huge amounts, the radioactivity contained in PG has measured in view of environmental radioactivity problem. In this work, the natural radioactivity in eighty PG samples taken from a stock near Samsun phosphoric fertilizer plant was measured by a high resolution gamma ray spectrometer. The mean activity of 226 Ra in PG samples has been found to be 546 Bq.kg -1 . However, the activities of 232 Th and 40 K measured in PG samples are negligibly small. In the presented paper, the gamma spectrometric method employed for this work is discussed and the radiological risk impact of radon gas emanation from 226 Ra mainly contained in PG, has been assessed

  14. Gamma spectrometric characterization of short cooling time nuclear spent fuels using hemispheric CdZnTe detectors

    CERN Document Server

    Lebrun, A; Szabó, J L; Arenas-Carrasco, J; Arlt, R; Dubreuil, A; Esmailpur-Kazerouni, K

    2000-01-01

    After years of cooling, nuclear spent fuel gamma emissions are mainly due to caesium isotopes which are emitters at 605, 662 and 796-801 keV. Extensive work has been done on such fuels using various CdTe or CdZnTe probes. When fuels have to be measured after short cooling time (during NPP outage) the spectrum is much more complex due to the important contributions of niobium and zirconium in the 700 keV range. For the first time in a nuclear power plant, four spent fuels of the Kozloduy VVER reactor no 4 were measured during outage, 37 days after shutdown of the reactor. In such conditions, good resolution is of particular interest, so a 20 mm sup 3 hemispheric crystal was used with a resolution better than 7 keV at 662 keV. This paper presents the experimental device and analyzes the results which show that CdZnTe commercially available detectors enabled us to perform a semi-quantitative determination of the burn-up after a short cooling time. In addition, it is discussed how a burn-up evolution code (CESAR)...

  15. Gas chromatographic-mass spectrometric determination of levodropropizine plasma levels in healthy volunteers.

    Science.gov (United States)

    Zaratin, P; De Angelis, L; Cattabeni, F

    1988-08-01

    A gas chromatographic-mass spectrometric method for the qualitative and quantitative analysis of levodropropizine (S(-)-3-(4-phenyl-piperazin-1-yl)-propane-1,2-diol, DF 526) in plasma is described. The method proved to be highly selective and sensitive. Drug concentrations as low as 5 ng/ml could be measured. Levodropropizine plasma levels were measured in 6 healthy volunteers after administration of an acute 60 mg dose. Peak concentrations were reached between 40 and 60 min and measurable amounts of drug were present till 8 h after administration.

  16. Application of a Gas Chromatography/Mass Spectrometric Method for the Determination of Butyltin Compounds in Sediment

    International Nuclear Information System (INIS)

    Chung, Min Young; Kim, Byung Joo; Yim, Yong Heon; So, Hun Young; Won, Yong Il; Jung, Pyong Gil; Kim, Yong Seong

    2004-01-01

    A gas chromatography/mass spectrometric (GC/MS) method has been developed for the determination of trace mono-n-butyltin (MBT), di-n-butyltin (DBT), and tri-n-butyltin (TBT) compounds in sediments. Samples were extracted by 10% acetic acid in methanol containing 0.03% tropolone and were then derivatized for GC/MS analysis. Ethylation by sodium tetraethylborate and phenylation by sodium tetraphenylborate were evaluated as a derivatization reaction of the organotins in sample extract. n-Hexane was added into reaction media in the beginning of the reaction for the continuous extraction of derivatized organotins. Ethylation requires less than 2 hours to get proper derivatization yields for MBT, DBT, and TBT altogether and produces relatively low amounts of side reaction products. Compared to ethylation, phenylation requires much longer time but provides relatively lower yield and produces considerable amounts of side reaction products. Therefore, the ethylation reaction was applied for the analysis of organotin compounds in sediment. An isotope dilution mass spectrometric (IDMS) method based on GC/MS has been applied to the accurate determination of DBT compounds in the sediments. The IDMS results from the analyses of sediment samples showed a reasonable repeatability and a good agreement with the values obtained by IDMS based on liquid chromatography/induced coupled plasma/mass spectrometry

  17. Calculation of critical level value for radioactivity detection in gamma spectrometric analysis on the base of semiconductor detectors under the Chernobyl' conditions in 1986-1987

    International Nuclear Information System (INIS)

    Glazunov, V.O.; Rusyaev, R.V.

    1989-01-01

    The problem of determination of radioactivity critical level in a sample by means of gamma spectrometer with semiconductor detector is studied theoretically. The formula for critical level, which shows that it is necessary to know the background pulse counting rate in order to determine the minimum gamma photon pulse counting rates, is derived. Calculations of critical level for the Chernobyl' conditions in time period from October 1986 till July 1987 are made. 8 refs.; 7 figs.; 17 tabs

  18. LC-APCI mass spectrometric method development and validation for the determination of atovaquone in human plasma.

    Science.gov (United States)

    Gurule, Sanjay; Goswami, Dipanjan; Khuroo, Arshad H; Monif, Tausif

    2010-05-01

    A newly developed LC-APCI mass spectrometric method is described for human plasma determination of atovaquone using lapachol internal standard. A single-step protein precipitation technique for plasma extraction of atovaquone achieving mean recovery of 94.17% (CV 8%) without compromising sensitivity (limit of quantitation 50.3 ng/mL) or linearity (50.3 ng/mL-23924.6 ng/mL) is delineated in this paper. Heated nebulizer in negative multiple reaction monitoring mode was employed with transitions m/z 365.2 --> m/z 337.1 and m/z 240.9 --> m/z 185.7 for atovaquone and lapachol respectively in this liquid chromatographic-tandem mass spectrometric method. Excellent chromatographic separation on a Synergi 4 micro Polar-RP 80A (150 x 2.0 mm) column, using 100 microL of plasma extraction volume along with 10 microL of injection load, completing analysis run-time within 2.5 min, highlights this simple yet unique bioanalytical method. The developed method can be successfully applied to pharmacokinetic studies on atovaquone suspension administered in healthy volunteers or HIV-infected patients. Moreover full method validation results not published before are presented and discussed in detail for the first time in this article. 2009 John Wiley & Sons, Ltd.

  19. Stabilization of spectra provided by a gamma-ray spectrometer. Application to the construction of a stabilizer; Stabilisation des spectres fournis par un spectrometre a rayons gamma. Application a la realisation d'un stabilisateur

    Energy Technology Data Exchange (ETDEWEB)

    Detourne, G. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1967-06-15

    This research is concerned with the stabilization of spectra provided by a gamma-ray spectrometer. It is required to hold the calibration straight line of the spectrometer in a position which is fixed initially to better than 5x10{sup -5} channel. A prototype numerical stabilizer has been constructed : the SPECTROSTAB; it is made up of two independent control loops; one of these makes the spectrometer gain depend on the derivatives of a reference peak at high energies; the other makes the origin of the energy scale depend on the derivatives of a second reference peak at low energies A theoretical study of the behaviour of a control loop shows that a direct action stabilizer gives the most accurate stabilization; the loss in resolving power on the theoretical peaks of the spectra attains about 1 % with a scintillation detector, and 10 % with a semi-conductor detector. Various tests show that the expected results are obtained and that the displacement of the spectral peaks produced by the derivatives are hidden by errors in the calculation of the peak abscissae. (author) [French] Cette etude a pour objet la stabilisation des spectres fournis par un spectrometre a rayons gamma. On veut maintenir la droite d'etalonnage du spectrometre dans une position fixee initialement a mieux de 6.10{sup -5} canal pres. On realise un prototype de stabilisateur numerique, le SPECTROSTAB; il comprend deux boucles d'asservissement independantes; l'une d'elles asservit le gain du spectrometre aux derives d'un pic de reference aux hautes energies; l'autre asservit l'origine de l'echelle des energies aux derives d'un second pic de reference aux basses energies. Une etude theorique du comportement d'une boucle d'asservissement montre qu'un stabilisateur a action directe permet la stabilisation la plus precise; la perte en resolution sur les pics theoriques des spectres atteint environ 1 % avec un detecteur a scintillateur et 10

  20. Application and evaluation of the mass spectrometric isotope dilution technique in the determination of rare earths in geological materials

    International Nuclear Information System (INIS)

    Moraes, N.M.P. de.

    1988-01-01

    Establishment of the experimental procedures employed in the rare earth element determination of geological samples by mass spectrometric isotope dilution analysis is discussed in the present work. The procedures involve preparation and calibration of the isotope tracers isotope dilution, dissolution in a teflon pressure vessel, chemical separation and isotope analysis using a fully automated Micromass VG ISOTOPES model 354 thermal ionization mass spectrometer. For the initial chemical separation of total rare earths the cationic resin was employed and HC1 and HNO 3 acids as eluents. In the second step rare earths elements were separated into individual (La, Ce and Nd) and subgroups (Sm-Eu-Gd, Yb-Er-Dy) fractions using the same cationic resin and α-HIBA as eluent. Nine elements La, Ce, Nd, Sm, Eu, Gd, Dy, Er and Yb are determined by this method in the ''United States Geological Survey'' (USGS) standard samples GSP-1, AGV-1 and G-2, with an overall precision of +- 1 to 2% and an accuracy of 5%. The concentration of rare earth element determined in the standard sample PCC-1 showed that the total analytical blanks are in submicrogram levels. The concentration of rare earth elements in the same USGS standard samples were also determined by Instrumental neutron activation analysis, neutron activation analysis with chemical separation before irradiation and inductively coupled argon plasma spectroscopy. The chemical procedures employed for these methods are the same as that used for mass spectrometric isotope dilution. Based on the results obtained, each method was evaluated pointing out their merits and defects. The study clearly showed that the chemical procedure employed for all these techniques was satisfactory. (author) [pt

  1. 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

  2. Cosmic gamma ray detection and discovery potential with the AMS-2 spectrometer; Detection de rayons {gamma} cosmiques et potentiel de decouvertes avec le spectrometre AMS-02

    Energy Technology Data Exchange (ETDEWEB)

    Girard, L

    2004-12-15

    Yet designed to measure charged component of the cosmic rays, the foreseen Alpha Magnetic Spectrometer (AMS-02) could also release {gamma}-ray studies, in the energy range from GeV to TeV, using the tracker system, for {gamma}-rays converted in e{sup +}e{sup -} pair, and the electromagnetic calorimeter. In the first part of the thesis are described the calibrations and the performances of the engineering model of the calorimeter, obtained from the analysis of data taken during a test-beam performed at CERN in July 2002. In the second part of the thesis, the AMS-02 discovery potential for {gamma}-astrophysics is presented. While exposure maps of the {gamma}--sky are computed for one year of data taking with the {gamma}--detectors, the acceptance of the calorimeter is obtained from Monte-Carlo simulations. The AMS-02 potential is then estimated for signals from the Vela pulsar and for some supersymmetric signals from the Galactic Center. (author)

  3. Determination of pyrethroid pesticide residues in processed fruits and vegetables by gas chromatography with electron capture and mass spectrometric detection.

    Science.gov (United States)

    Sannino, Anna; Bandini, Mirella; Bolzoni, Luciana

    2003-01-01

    A gas chromatographic method was developed for the simultaneous determination of 12 pyrethroids (tefluthrin, bifenthrin, fenpropathrin, cyhalothrin, permethrin, cyfluthrin, cypermethrin, alpha-cypermethrin, flucythrinate, fenvalerate, fluvalinate, and deltamethrin) in tomato puree, peach nectar, orange juice, and canned peas. A miniaturized extraction-partition procedure requiring small amounts of nonchlorinated solvents is used. Samples are extracted with acetone, partitioned with ethyl acetate-cyclohexane (50 + 50, v/v), and cleaned up on a Florisil cartridge. The final extract is analyzed by gas chromatography with both electron capture and mass spectrometric detection modes. Studies at fortification levels of 0.010-0.100 mg/kg gave mean recoveries ranging from 70.2 to 96.0% and coefficients of variation between 4.0 and 13.9% for all compounds. Quantitation limits were < 0.010 mg/kg for electron capture detection.

  4. Development of an Isotope-Dilution Liquid Chromatography/Mass Spectrometric Method for the Accurate Determination of Acetaminophen in Tablets

    Energy Technology Data Exchange (ETDEWEB)

    Shin, Hyun Ju; Kim, Byung Joo; Lee, Joon Hee; Hwang, Eui Jin [Korea Research Institute of Standards and Science, Daejeon (Korea, Republic of)

    2010-12-15

    Acetaminophen (N-acetyl-p-aminophenol) is one of the most popular analgesic and antipyretic drugs. An isotope dilution mass spectrometric method based on LC/MS was developed as a candidate reference method for the accurate determination of acetaminophen in pharmaceutical product. After spiking an isotope labeled acetaminophen (acetyl-{sup 13}C{sub 2}, {sup 15}Nacetaminophen) as an internal standard, tablet extracts were analyzed by LC/MS in a selected reaction monitoring (SRM) mode to detect ions at m/z 152→110 and m/z 155→111 for acetaminophen and acetyl-{sup 13}C{sub 2}, {sup 15}N-acetaminophen, respectively. The repeatability and reproducibility of the developed ID/LC-MS method were tested for the validation and assessment of metrological quality of the method.

  5. Simultaneous determination of oxygen, nitrogen and hydrogen in metals by pulse heating and time of flight mass spectrometric method.

    Science.gov (United States)

    Shen, Xuejing; Wang, Peng; Hu, Shaocheng; Yang, Zhigang; Ma, Hongquan; Gao, Wei; Zhou, Zhen; Wang, Haizhou

    2011-05-30

    The inert gas fusion and infrared absorption and thermal conductivity methods are widely used for quantitative determination of oxygen(O), nitrogen(N) and hydrogen(H) in metals. However, O, N and H cannot be determined simultaneously with this method in most cases and the sensitivity cannot meet the requirement of some new metal materials. Furthermore, there is no equipment or method reported for determination of Argon(Ar) or Helium(He) in metals till now. In this paper, a new method for simultaneous quantitative determination of O, N, H and Ar(or He) in metals has been described in detail, which combined the pulse heating inert gas fusion with time of flight mass spectrometric detection. The whole analyzing process was introduced, including sample retreatment, inert gas fusion, mass spectral line selection, signal acquisition, data processing and calibration. The detection limit, lower quantitative limit and linear range of each element were determined. The accuracy and precision of the new method have also been verified by measurements of several kinds of samples. The results were consistent with that obtained by the traditional method. It has shown that the new method is more sensitive and efficient than the existing method. Copyright © 2011 Elsevier B.V. All rights reserved.

  6. Problems involved in quantitative gamma, camera scintigraphy. B. Determination of the optimal spectrometric window

    International Nuclear Information System (INIS)

    Soussaline, F.; Ricard, S.; Raynaud, C.

    1976-01-01

    By means of suitable equipment including a delay line camera and an on-line data processing system with energy coding for each photon, a preliminary study of the camera response versus energy in terms of dispersion function can explain the consequences of the choice of window on the resolution and sensitivity. Using the results of other authors on the optimization of low-energy windows based on largely subjective criteria, the kidney 197 HgCl 2 uptake values for a series of 25 patients were calculated in four digital windows of different widths and variable thresholds. From these results it was possible to estimate the relative error in each case and to choose a 25% window with a threshold corresponding to the photopeak maximum [fr

  7. Automatized facility for express gamma-spectrometric studies of full-size core and muds of oil-gas wells

    International Nuclear Information System (INIS)

    Antropov, S.Yu.; Ermilov, A.P.; Ermilov, S.A.; Komarov, N.A.; Krokhin, I.I.

    2005-01-01

    In the automatized facility 'Sputnik-Geo' for automated core feeding of the conveyor belt with 5 m length is using. Activity measurement has being conducted by four scintillation gamma radiation detectors. Symmetrical location of the detectors relatively the core allows to exclude of the geometrical uncertainty of component. The spectrum processing and the control by conveyor engine are carried out by computer, which preserves the results of measurements in the database. For density measurement the scintillation detector with collimated source on the 137 Cs radionuclide base is applied. The facility is provided with the light-diode coefficient stabilization of detector amplification, that permits to operation time increase without spectrometers requalification by energy up to 1 working day

  8. Mass spectrometric determination of magnesium isotopic ratios and its corrections for electron multiplier discrimination and mass fractionation

    International Nuclear Information System (INIS)

    Deng Zhongguo

    1989-01-01

    The mass spectrometric determination of magnesium isotopic ratios by the use of uranyl nitrate added to magnesium samples to act as a binding agent is reported. Prebaking empty filaments and preheating filaments with deposited magnesium samples on its surface in a vacuum are employed to reduce the Na signal from the thenium-ribbon. Methods for correcting magnesium isotopic ratios for electron multiplier discrimination and mass fractionation are described in detail. The results of the determination of natural magnesium isotopic ratios are 25 Mg/ 24 Mg = 0.12660 (1±0.01%) and 26 Mg/ 24 Mg = 0.13938 (1±0.10%). The magnesium isotopic ratios of rich - 26 Mg-2 sample and rich- 25 Mg-1 sample are 24 Mg/ 26 Mg = 0.003463 (1±0.2%), 25 Mg/ 26 Mg = 0.001656 (±0.2%) and 24 Mg/ 25 Mg = 0.006716 (1±0.2%), 26 Mg/ 25 Mg = 0.007264 (1±0.2%) respectively

  9. Atomic-absorption spectrometric determination of cobalt, nickel, and copper in geological materials with matrix masking and chelation-extraction

    Science.gov (United States)

    Sanzolone, R.F.; Chao, T.T.; Crenshaw, G.L.

    1979-01-01

    An atomic-absorption spectrometric method is reported for the determination of cobalt, nickel, and copper in a variety of geological materials including iron- and manganese-rich, and calcareous samples. The sample is decomposed with HP-HNO3 and the residue is dissolved in hydrochloric acid. Ammonium fluoride is added to mask iron and 'aluminum. After adjustment to pH 6, cobalt, nickel, and copper are chelated with sodium diethyl-dithiocarbamate and extracted into methyl isobutyl ketone. The sample is set aside for 24 h before analysis to remove interferences from manganese. For a 0.200-g sample, the limits of determination are 5-1000 ppm for Co, Ni, and Cu. As much as 50% Fe, 25% Mn or Ca, 20% Al and 10% Na, K, or Mg in the sample either individually or in various combinations do not interfere. Results obtained on five U.S. Geological Survey rock standards are in general agreement with values reported in the literature. ?? 1979.

  10. Burnup determination of a high burnup PWR fuel by neodymium and cesium isotope monitor methods based on isotope dilution mass spectrometric measurements

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jung Suk; Jeon, Young Shin; Park, Soon Dal; Han, Sun Ho; Ha, Yeong Keong; Song, Kyu Seok [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2008-11-15

    Destructive methods were used for the burnup determination of a PWR nuclear fuel irradiated to a high burnup in power reactors. The total burnup was determined from a measurement of the Nd and Cs isotope burnup monitors. The methods included U, Pu, {sup 148}Nd, {sup 145}Nd+{sup 146}Nd, total of the Nd isotopes, and {sup 133}Cs and {sup 137}Cs determinations by the isotope dilution mass spectrometric method (IDMS) by using quadrupole spikes ({sup 233}U, {sup 242}Pu, {sup 150}Nd and {sup 133}Cs). The methods involved two sequential anion exchange resin (AG 1X8 and 1X4) separation procedures and a Cs purification with a cation exchange resin (AG 50WX4) separation procedure. The effective fission yield was calculated from the weighted fission yields averaged over the irradiation period. The results obtained by the Nd and Cs isotopes from the mass spectrometric measurement were compared with those by the ORIGEN code.

  11. Microdiffusion-based UV-LED spectrometric setup for determining low levels of ethanol in fruit juice.

    Science.gov (United States)

    Gros, Nataša

    2011-12-15

    A novel setup is described in which we combined the separation of a volatile substance from a sample with a complex matrix on the basis of a microdiffusion process with a kinetic on-line spectrometric monitoring of the reaction in the receptive medium at 365 nm. The fruit juice was selected as a model for testing the performance of the setup in real-life applications. The ethanol content in fruit juice can be considered as an indicator of the fruit-juice quality and should not exceed the regulatory limiting values. After optimising the microdiffusion process, blackcurrant, orange and two varieties of apple juice were analysed. The sample analysis lasted 15 min at 35°C. The ethanol concentrations were found to be between 0.9 and 4.0 mmol/L, and were comparable to the results obtained using the SIST:ISO 2448:1998 standard method, which is time consuming, labour intensive and requires high sample volumes. The setup can easily be adapted for determining other volatile substances in low concentrations in complicated samples of different types by introducing different chemistry and replacing the light source if the light of a different wavelength is required. The measuring characteristics of the setup were critically assessed, the main sources of uncertainty recognised and the possibilities for further improvements of the setup and the procedure considered. Copyright © 2011 Elsevier B.V. All rights reserved.

  12. Gas chromatography-mass spectrometric determination of traces of ether-type icing inhibitors in free-floating fuels

    Energy Technology Data Exchange (ETDEWEB)

    Shin, H.S. [Dept. of Environmental Education, Kongju National Univ., Kongju (Korea); Abuse Drug Research Center, Kongju National Univ., Kongju (Korea); Ahn, H.S. [Dept. of Environmental Science, Kongju National Univ., Kongju (Korea)

    2004-08-01

    A gas chromatographic-mass spectrometric (GC-MS) assay method has been developed for simultaneous determination of ethylene glycol monomethyl ether (EGME) and diethylene glycol monomethly ether (DEGME) in spilled aviation fuels. Ethylene glycol monobutyl ether (EGBE) and ethylene glycol monoethyl ether (EGEE) were used as internal standard and surrogate, respectively. Sample preparation consisted of back-extraction with 7 mL dichloromethane after extraction of 50 mL of fuel with 2 mL of water. The extract was concentrated to dryness, dissolved in 100 {mu}L methanol, and analyzed by GC-MS with selected-ion monitoring (SIM). The peaks had good chromatographic properties on a semi-polar column. EGME and DEGME were extracted from fuel with high recovery of 75 and 85%, with small variations, respectively. Method detection limits were 1.3 and 1.0 ng mL{sup -1} for EGME and DEGME, respectively, in spilled fuel. DEGME was detected at concentrations of 22.6 and 19.7 ng mL{sup -1} in two samples from among five free-floating samples collected in a tunnel of a subway station located in the vicinity of an army base in Korea. The method might be useful for differentiation between the fuel-types kerosene and JP-8, which might originate from a storage tank. (orig.)

  13. Gas Chromatographic-Selected Ion Monitoring-Mass Spectrometric Determination of Cigarette Mainstream Smoke Components with Sensory Attributes

    Directory of Open Access Journals (Sweden)

    Coleman WM

    2014-12-01

    Full Text Available A new method has been developed that detects significant quantitative differences in the amounts of pyrazines, pyridines, furfurals, carboxylic acids, b-damascenone, sclareolide, and megastigmatrienones in the mainstream smoke of a series of five commercial cigarettes. This new quantitative method is based on the gas chromatographic-selected ion monitoring-mass spectrometric (GC-SIM-MS determination of the selected smoke constituents. The accuracy and precision of the approach were well within acceptable parameters with the majority of cases relative standard deviation (RSD values consistently around 5%. Sample preparation was simple requiring only the dissolution of the trapped particulate material in a known volume of methanol followed by injection of this clear dark colored solution into the gas chromatograph. This approach represents an advance in the technology in terms of higher sample throughput and less sample workup. Certain products demonstrated consistent trends in concentration of specific chemical classes. The mainstream smoke from a University of Kentucky reference cigarette, 2R4F, was included for reference purposes. These results are applicable in the overall evaluation of the components responsible for the taste associated with cigarette products.

  14. Determination of nuclear fuel burn-up using mass spectrometric techniques

    International Nuclear Information System (INIS)

    Saha, B.; Bagyalakshmi, R.; Periaswami, G.; Kavimandan, V.D.; Chitambar, S.A.; Jain, H.C.; Mathews, C.K.

    1977-01-01

    Determination of burn-up using a stable fission product monitor such as 148 Nd and heavy elements, determined by isotope dilution mass spectrometry gives the most accurate data. This report describes the work carried out to standardise the conditions for burn-up determination. Some typical results are given. (author)

  15. X-ray spectrometric determination of glass content of melts incorporating radioactive waste: a feasibility study

    International Nuclear Information System (INIS)

    Slates, R.V.

    1978-09-01

    X-ray fluorescence spectrometry was evaluated for the determination of glass content and homogeneity of glass incorporating high-level radioactive waste. Accuracy and precision were determined for analyses of Al 2 O 3 , SiO 2 , CaO, TiO 2 , MnO, Fe 2 O 3 , and NiO in specimens of known composition. These specimens were prepared by fusing powdered glass with nonradioactive synthetic waste. Matrix effects of sodium on these analyses were specifically evaluated. X-ray fluorescence spectrometry was shown to be applicable to the proposed determinations by comparing the known glass contents of 14 glass waste compositions with those calculated from experimentally determined concentrations of SiO or TiO 2

  16. Gas Chromatographic-Mass Spectrometric Determination of British Anti-Lewisite in Plasma

    National Research Council Canada - National Science Library

    Byers, C. E; Holloway, E. R; Korte, W. D; Smith, J. R; Clarkson, E. D; Platoff, G. E; Capacio, B. R

    2004-01-01

    British anti-Lewisite (BAL) (2,3-dimercapto-1-propanol) is a potential therapeutic compound when used against the effects of cutaneous sulfur mustard, and a method for its determination in plasma has been developed...

  17. Self-attenuation corrections calculated by LabSOCS Simulations for gamma-spectrometric measurements with HPGe detectors

    International Nuclear Information System (INIS)

    Tian Zining; Ouyang Xiaoping; Liu Yang; Chen Liang; Liu Jinliang; Zhang Xianpeng; Song Jiwen; Zeng Ming

    2014-01-01

    Simulations from Laboratory Sourceless Object Counting System (LabSOCS) software were used to determine self-attenuation correction factor, which is defined as the efficiency ratio of the sample with the absorbing medium to that of the sample without absorbing medium. The semi-empirical self-attenuation correction formula F(μ) used to correct self-attenuation of a sample was applied. A comparison of the two methods reveals that formula of sample with φ75 mm × 25 mm and φ75 mm × 10 mm can be, respectively, used in the self-attenuation correction for μ in the ranges of 0 to 0.5 cm -1 and 0.5 cm -1 to 2.0 cm -1 , indicating that the semi-empirical formula will not be used when μ has exceeded the interval. The semi-empirical formula value is consistent with the experimental value, within 7.9% accuracy. Therefore, this method is correct and effective. Both of our two methods can accurately produce a relative self-attenuation correction factor when the composition of the sample is known. The self-attenuation correction of a sample with unknown composition can only be carried out using a semi-empirical formula method. (authors)

  18. 134Cs emission probabilities determination by gamma spectrometry

    Science.gov (United States)

    de Almeida, M. C. M.; Poledna, R.; Delgado, J. U.; Silva, R. L.; Araujo, M. T. F.; da Silva, C. J.

    2018-03-01

    The National Laboratory for Ionizing Radiation Metrology (LNMRI/IRD/CNEN) of Rio de Janeiro performed primary and secondary standardization of different radionuclides reaching satisfactory uncertainties. A solution of 134Cs radionuclide was purchased from commercial supplier to emission probabilities determination of some of its energies. 134Cs is a beta gamma emitter with 754 days of half-life. This radionuclide is used as standard in environmental, water and food control. It is also important to germanium detector calibration. The gamma emission probabilities (Pγ) were determined mainly for some energies of the 134Cs by efficiency curve method and the Pγ absolute uncertainties obtained were below 1% (k=1).

  19. Gas Chromatographic Mass Spectrometric Determination of Myo-inositol in Humans Utilizing a Deuterated Internal Standard

    DEFF Research Database (Denmark)

    Andersen, Jan Rud; Larsen, Elfinn; Harbo, Helge

    1982-01-01

    The isotopic dilution technique was used for determining the content of myo-inositol in human urine, plasma and haemolysed erythrocyte samples. A deuterated myo-inositol, synthesized from inosose-2 by base-catalysed exchange of hydrogens by deuterium, followed by reduction of the inosose with 2H2...

  20. Confirmation of the correct application of the gamma spectrometric method carried out in the Cuban Center for Radiation Protection and Hygiene

    International Nuclear Information System (INIS)

    Fernandez Gomez, Isis M.; Carrazana Gonzalez, Jorge A.; Capote Ferrera, Eduardo

    2008-01-01

    One of the technical requirements of the standard ISO/IEC 17025:2006 is that the laboratories that use standard methods shall confirm that they can properly operate these before introducing the tests or calibrations. Among the testing activities that execute the Environmental Radiological Surveillance Laboratory of the Cuban Center for Radiation Protection and Hygiene, is the determination of gamma radionuclides by gamma spectrometry with HPGe detectors. This test has been accredited by the Cuban Accreditation Body, according to the standard ISO/IEC 17025:2005. Fulfilling the requirements of this standard, regarding the selection of methods, the laboratory uses internationally standard method for its gamma spectrometry determinations. For this reason it was necessary to confirm the correct application of the selected method before incorporating it as scientific-technical service that the institution offers. With this purpose the method confirmation using certified reference materials of different matrixes and for the different geometries used in the laboratory were carried out. The obtained results of this study were processed statistically to check the precision and trueness of the same ones. In this sense, the laboratory participates periodically in interlaboratory comparison programs that include the radionuclides analysis by gamma spectrometry, as another form of accuracy confirmation of the results that the laboratory reports. In this paper the design of the realized intralaboratory study, as well as the results of it are presented. From the obtained results in the realized study, as well as from the interlaboratory comparison programs, it is possible to conclude that the method used in the laboratory is executed appropriately and it is under control. (author)

  1. Raman spectrometric determination of Pu(VI) and Pu(V) in nitric acid solutions

    International Nuclear Information System (INIS)

    Gantner, E.; Freudenberger, M.; Steinert, D.; Ache, H.J.

    1987-03-01

    The determination of Pu(VI) in nitric acid solutions by spontaneous Laser Raman Spectrometry (LRS) was investigated and a calibration curve was established using U(VI) as internal standard. In addition, the concentrations of Pu(VI) and Pu(V) as a function of time were measured by this method in Pu(VI) solutions of different acidity containing H 2 O 2 as the reducing agent. In solutions which are intensely coloured by the presence of Ru(NO) complexes Pu(VI) can also be determined by LRS using a Kr + laser as excitation source. In future experiments, the study of the Pu(IV)-interaction with Ru using LRS and spectrophotometry as analytical techniques is therefore intended. (orig.) [de

  2. Fragment Formula Calculator (FFC): Determination of Chemical Formulas for Fragment Ions in Mass Spectrometric Data

    OpenAIRE

    Wegner, André; Weindl, Daniel; Jäger, Christian; Sapcariu, Sean C.; Dong, Xiangyi; Stephanopoulos, Gregory; Hiller, Karsten

    2014-01-01

    The accurate determination of mass isotopomer distributions (MID) is of great significance for stable isotope-labeling experiments. Most commonly, MIDs are derived from gas chromatography/electron ionization mass spectrometry (GC/EI-MS) measurements. The analysis of fragment ions formed during EI, which contain only specific parts of the original molecule can provide valuable information on the positional distribution of the label. The chemical formula of a fragment ion is usually applied to ...

  3. On-line Incorporation of Cloud Point Extraction in Flame Atomic Absorption Spectrometric Determination of Silver

    OpenAIRE

    DALALI, Nasser; JAVADI, Nasrin; AGRAWAL, Yadvendra KUMAR

    2008-01-01

    A cloud point extraction method was incorporated into a flow injection system, coupled with flame atomic absorption spectrometry, for determination of trace amounts of silver. The analyte in the aqueous solution was acidified with 0.2 mol L-1 sulfuric acid and complexed with dithizone. The cloud point extraction was performed using the non-ionic surfactant Triton X-114. After obtaining the cloud point, the surfactant-rich phase containing the dithizonate complex was collected in a m...

  4. Microwave plasma atomic emission spectrometric determination of Ca, K and Mg in various cheese varieties.

    Science.gov (United States)

    Ozbek, Nil; Akman, Suleyman

    2016-02-01

    Microwave plasma-atomic emission spectrometry (MP-AES) was used to determine calcium, magnesium and potassium in various Turkish cheese samples. Cheese samples were dried at 100 °C for 2 days and then digested in a mixture of nitric acid/hydrogen peroxide (3:1). Good linearities (R(2) > 0.999) were obtained up to 10 μg mL(-1) of Ca, Mg and K at 445.478 nm, 285.213 nm and 766.491 nm, respectively. The analytes in a certified reference milk powder sample were determined within the uncertainty limits. Moreover, the analytes added to the cheese samples were recovered quantitatively (>90%). All determinations were performed using aqueous standards for calibration. The LOD values for Ca, Mg and K were 0.036 μg mL(-1), 0.012 μg mL(-1) and 0.190 μg mL(-1), respectively. Concentrations of Ca, K and Mg in various types of cheese samples produced in different regions of Turkey were found between 1.03-3.70, 0.242-0.784 and 0.081-0.303 g kg(-1), respectively. Copyright © 2015 Elsevier Ltd. All rights reserved.

  5. A mass spectrometric method to determine activities of enzymes involved in polyamine catabolism

    International Nuclear Information System (INIS)

    Moriya, Shunsuke; Iwasaki, Kaori; Samejima, Keijiro; Takao, Koichi; Kohda, Kohfuku; Hiramatsu, Kyoko; Kawakita, Masao

    2012-01-01

    Highlights: ► Compounds in polyamine catabolic pathway were determined by a column-free ESI-TOF MS. ► N 1 - and N 8 -acetylspermidine were determined by a column-free ESI-MS/MS. ► The method was applied to determine activities of APAO, SMO, and SSAT in the pathway. ► The assay method contained stable isotope-labeled natural substrates. ► It is applicable to biological samples containing natural substrate and product. - Abstract: An analytical method for the determination of three polyamines (putrescine, spermidine, and spermine) and five acetylpolyamines [N 1 -acetylspermidine (N 1 AcSpd), N 8 -acetylspermidine (N 8 AcSpd), N 1 -acetylspermine, N 1 ,N 8 -diacetylspermidine, and N 1 ,N 12 -diacetylspermine] involved in the polyamine catabolic pathway has been developed using a hybrid tandem mass spectrometer. Heptafluorobutyryl (HFB) derivatives of these compounds and respective internal standards labeled with stable isotopes were analyzed simultaneously by TOF MS, based on peak areas appearing at appropriate m/z values. The isomers, N 1 AcSpd and N 8 AcSpd were determined from their fragment ions, the acetylamidopropyl and acetylamidobutyl groups, respectively, using MS/MS with 13 C 2 -N 1 AcSpd and 13 C 2 -N 8 AcSpd which have the 13 C 2 -acetyl group as an internal standard. The TOF MS method was successfully applied to measure the activity of enzymes involved in polyamine catabolic pathways, namely N 1 -acetylpolyamine oxidase (APAO), spermine oxidase (SMO), and spermidine/spermine N 1 -acetyltransferase (SSAT). The following natural substrates and products labeled with stable isotopes considering the application to biological samples were identified; for APAO, [4,9,12- 15 N 3 ]-N 1 -acetylspermine and [1,4,8- 15 N 3 ]spermidine ( 15 N 3 -Spd), respectively; for SMO, [1,4,8,12- 15 N 4 ]spermine and 15 N 3 -Spd, respectively; and for SSAT, 15 N 3 -Spd and [1,4,8- 15 N 3 ]-N 1 -acetylspermidine, respectively.

  6. A mass spectrometric method to determine activities of enzymes involved in polyamine catabolism

    Energy Technology Data Exchange (ETDEWEB)

    Moriya, Shunsuke; Iwasaki, Kaori [Department of Molecular Medicine, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kami-kitazawa, Setagaya-ku, Tokyo 156-8506 (Japan); Samejima, Keijiro, E-mail: samejima-kj@igakuken.or.jp [Department of Molecular Medicine, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kami-kitazawa, Setagaya-ku, Tokyo 156-8506 (Japan); Takao, Koichi [Faculty of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama 350-0295 (Japan); Kohda, Kohfuku [Research Institute of Pharmaceutical Sciences, Musashino University, 1-1-20 Shinmachi, Nishitokyo, Tokyo 202-8585 (Japan); Hiramatsu, Kyoko; Kawakita, Masao [Department of Molecular Medicine, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kami-kitazawa, Setagaya-ku, Tokyo 156-8506 (Japan)

    2012-10-20

    Highlights: Black-Right-Pointing-Pointer Compounds in polyamine catabolic pathway were determined by a column-free ESI-TOF MS. Black-Right-Pointing-Pointer N{sup 1}- and N{sup 8}-acetylspermidine were determined by a column-free ESI-MS/MS. Black-Right-Pointing-Pointer The method was applied to determine activities of APAO, SMO, and SSAT in the pathway. Black-Right-Pointing-Pointer The assay method contained stable isotope-labeled natural substrates. Black-Right-Pointing-Pointer It is applicable to biological samples containing natural substrate and product. - Abstract: An analytical method for the determination of three polyamines (putrescine, spermidine, and spermine) and five acetylpolyamines [N{sup 1}-acetylspermidine (N{sup 1}AcSpd), N{sup 8}-acetylspermidine (N{sup 8}AcSpd), N{sup 1}-acetylspermine, N{sup 1},N{sup 8}-diacetylspermidine, and N{sup 1},N{sup 12}-diacetylspermine] involved in the polyamine catabolic pathway has been developed using a hybrid tandem mass spectrometer. Heptafluorobutyryl (HFB) derivatives of these compounds and respective internal standards labeled with stable isotopes were analyzed simultaneously by TOF MS, based on peak areas appearing at appropriate m/z values. The isomers, N{sup 1}AcSpd and N{sup 8}AcSpd were determined from their fragment ions, the acetylamidopropyl and acetylamidobutyl groups, respectively, using MS/MS with {sup 13}C{sub 2}-N{sup 1}AcSpd and {sup 13}C{sub 2}-N{sup 8}AcSpd which have the {sup 13}C{sub 2}-acetyl group as an internal standard. The TOF MS method was successfully applied to measure the activity of enzymes involved in polyamine catabolic pathways, namely N{sup 1}-acetylpolyamine oxidase (APAO), spermine oxidase (SMO), and spermidine/spermine N{sup 1}-acetyltransferase (SSAT). The following natural substrates and products labeled with stable isotopes considering the application to biological samples were identified; for APAO, [4,9,12-{sup 15}N{sub 3}]-N{sup 1}-acetylspermine and [1,4,8-{sup 15}N{sub 3

  7. Mass spectrometric determination of the thermodynamic excess properties of ternary Fe-Co-Cr melts

    International Nuclear Information System (INIS)

    Schmidt, Harald; Tomiska, Josef

    2004-01-01

    Computer-aided Knudsen cell mass spectrometry is used for the thermodynamic investigations on ternary Fe-Co-Cr melts over the entire range of composition. The thermodynamic mixing behavior has been determined by means of the 'digital intensity-ratio' (DIR) method. The ternary thermodynamically adapted power (TAP) series concept is used for the algebraic representation of the molar excess properties. The corresponding TAP parameters, and the values of the molar excess quantities Z E (T, x) (Z is the Gibbs energy G, heat of mixing H, entropy S) as well as the thermodynamic activities of all three constituents at 1950 K are presented

  8. Determination of cilnidipine, a new calcium antagonist, in human plasma using high performance liquid chromatography with tandem mass spectrometric detection.

    Science.gov (United States)

    Zhang, Xianhua; Zhai, Suodi; Zhao, Rongsheng; Ouyang, Jin; Li, Xiaoguang; Baeyens, Willy R G

    2007-09-26

    A rapid, sensitive and reliable high performance liquid chromatographic method coupled with tandem mass spectrometry (HPLC-MS/MS) has been developed and validated for the determination of cilnidipine, a relatively new calcium antagonist, in human plasma. The reversed-phase chromatographic system was interfaced with a TurboIonSpray (TIS) source. Nimodipine was employed as the internal standard (IS). Sample extracts following protein precipitation were injected into the HPLC-MS/MS system. The analyte and IS were eluted isocratically on a C18 column, with a mobile phase consisting of CH(3)OH and NH(4)Ac (96:4, v/v). The ions were detected by a triple quadrupole mass spectrometric detector in the negative mode. Quantification was performed using multiple reaction monitoring (MRM) of the transitions m/z 491.2-->122.1 and m/z 417.1-->122.1 for cilnidipine and for the IS, respectively. The analysis time for each run was 3.0 min. The calibration curve fitted well over the concentration range of 0.1-10 ngmL(-1), with the regression equation Y=(0.103+/-0.002)X+(0.014+/-0.003) (n=5), r=0.9994. The intra-day and inter-day R.S.D.% were less than 12.51% at all concentration levels within the calibration range. The recoveries were between 92.71% and 97.64%. The long-term stability and freeze-thaw stability were satisfying at each level. The present method provides a modern, rapid and robust tool for pharmacokinetic studies of cilnidipine.

  9. Mass spectrometric determination of the predominant adrenergic protoalkaloids in bitter orange (Citrus aurantium).

    Science.gov (United States)

    Nelson, Bryant C; Putzbach, Karsten; Sharpless, Katherine E; Sander, Lane C

    2007-11-28

    The predominant adrenergic protoalkaloid found in the peel and fruit of bitter orange, Citrus aurantium, is synephrine. Synephrine is reputed to have thermogenic properties and is used as a dietary supplement to enhance energy and promote weight loss. However, there exists some concern that the consumption of dietary supplements containing synephrine or similar protoalkaloids may contribute to adverse cardiovascular events. This study developed and validated a positive-ion mode liquid chromatography/tandem mass spectrometry (LC/MS/MS) method for the quantitative determination of the major (synephrine) and minor (tyramine, N-methyltyramine, octopamine, and hordenine) adrenergic protoalkaloids in a suite of National Institute of Standards and Technology (NIST) bitter orange Standard Reference Materials (SRMs): SRM 3258 Bitter Orange Fruit, SRM 3259 Bitter Orange Extract, and SRM 3260 Bitter Orange Solid Oral Dosage Form. The limit of quantitation (LOQ) for all protoalkaloids is approximately 1 pg on-column, except for octopamine (20 pg on-column). Additionally, the method has a linear dynamic range of > or =3 orders of magnitude for all of the protoalkaloids. Individual, as well as "total", protoalkaloid levels (milligrams per kilogram) in the NIST SRMs were determined and compared to the levels measured by an independent liquid chromatography/fluorescence detection (LC/FD) method. Satisfactory concordance between the LC/MS/MS and LC/FD protoalkaloid measurements was demonstrated. LC/MS/MS analysis of the protoalkaloids in the SRMs resulted in mean measurement imprecision levels of < or =10% coefficient of variation (% CV).

  10. An indirect atomic absorption spectrometric determination of ciprofloxacin, amoxycillin and diclofenac sodium in pharmaceutical formulations

    Directory of Open Access Journals (Sweden)

    MAHMOUD MOHAMED ISSA

    2008-05-01

    Full Text Available A highly sensitive indirect atomic absorption spectrophotometric (AAS method has been developed for the determination of very low concentrations of ciprofloxacin, amoxycillin and diclofenac sodium. The method is based on the oxidation of these drugs with iron(III. The excess of iron(III was extracted into diethyl ether and then the iron(II in the aqueous layer was aspirated into an air–acetylene flame and determined by AAS. The linear concentration ranges were 25–400, 50–500 and 60–600 ng ml-1 for ciprofloxacin, amoxycillin and diclofenac sodium, respectively. The results were statistically compared with the official method using t- and f-test at p < 0.05. There were insignificant interferences from most of the excipients present. The intra- and inter-day assay coefficients of variation were less than 6.1 % and the recoveries ranged from 95 to 103 %. The method was applied for the analysis of these drug substances in their commercial pharmaceutical formulations.

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

    International Nuclear Information System (INIS)

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

    1988-01-01

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

  12. Determination of sirolimus in rabbit arteries using liquid chromatography separation and tandem mass spectrometric detection.

    Science.gov (United States)

    Zhang, Jun; Rodila, Ramona; Watson, Pamela; Ji, Qin; El-Shourbagy, Tawakol A

    2007-10-01

    Sirolimus, an effective immunosuppressive agent, is used for drug eluting stents. During stent development, an analytical method for the determination of sirolimus in tissue needs to be established. Normally, tissue samples are homogenized and then analyzed against the calibration standards prepared in a tissue homogenate. This approach provides insufficient control of the homogenization process. In this paper, tissue quality control samples were introduced for the optimization of the homogenization process during method development, but also allowance for the performance evaluation of the entire analytical process. In addition, a new approach using rabbit blood as a homogenization medium was developed to stabilize sirolimus in rabbit tissue homogenates. Calibration standards and quality controls were prepared by spiking different sirolimus working solutions into rabbit blood. Homogenization quality control samples were prepared by injecting other sirolimus working solutions into empty test tubes and pre-cut arteries within pre-defined masses. A high-throughput homogenization procedure was optimized based on the specific chemical properties of sirolimus. The linear dynamic range was between 49.9 pg/mL and 31.9 ng/mL to accommodate the expected artery homogenate concentrations. Additionally, quality controls in rabbit blood were also used in the extraction to support the calibration standards. The accuracy and precision of the quality controls in rabbit blood reflect the extraction performance and the accuracy and precision of the homogenization tissue quality controls reflect the overall performance of the method. The mean bias was between -4.5 and 0.2% for all levels of quality controls in the blood and between 4.8 and 14.9% for all levels of the homogenization tissue quality controls. The CVs of all concentration levels were < or =5.3% for the quality controls in blood and < or =9.2% for the homogenization tissue quality controls. The method was successfully

  13. A comparison of reliability of soil Cd determination by standard spectrometric methods

    Science.gov (United States)

    McBride, M.B.

    2015-01-01

    Inductively coupled plasma emission spectrometry (ICP-OES) is the most common method for determination of soil Cd, yet spectral and matrix interferences affect measurements at the available analytical wavelengths for this metal. This study evaluated the severity of the interference over a range of total soil Cd by comparing ICP-OES and ICP-MS measurements of Cd in acid digests. ICP-OES using the emission at 226.5 nm generally unable to quantify soil Cd at low (near-background) levels, and gave unreliable values compared to ICP-MS. Using the line at 228.nm, a marked positive bias in Cd measurement (relative to the 226.5 nm measurement) was attributable to As interference even at soil As concentrations below 10 mg/kg. This spectral interference in ICP-OES was severe in As-contaminated orchard soils, giving a false value for soil total Cd near 2 mg kg−1 when soil As was 100–150 mg kg−1. In attempting to avoid these ICP emission-specific interferences, we evaluated a method to estimate total soil Cd using 1 M HNO3 extraction followed by determination of Cd by flame atomic absorption (FAA), either with or without pre-concentration of Cd using an Aliquat-heptanone extractant. The 1 M HNO3 extracted an average of 82% of total soil Cd. The FAA method had no significant interferences, and estimated the total Cd concentrations in all soils tested with acceptable accuracy. For Cd-contaminated soils, the Aliquat-heptanone pre-concentration step was not necessary, as FAA sensitivity was adequate for quantification of extractable soil Cd and reliable estimation of total soil Cd. PMID:22031569

  14. Dose Rate Determination from Airborne Gamma-ray Spectra

    DEFF Research Database (Denmark)

    Bargholz, Kim

    1996-01-01

    The standard method for determination of ground level dose rates from airborne gamma-ray is the integral count rate which for a constant flying altitude is assumed proportional to the dose rate. The method gives reasonably results for natural radioactivity which almost always has the same energy...

  15. Determination of gaussian peaks in gamma spectra by iterative regression

    International Nuclear Information System (INIS)

    Nordemann, D.J.R.

    1987-05-01

    The parameters of the peaks in gamma-ray spectra are determined by a simple iterative regression method. For each peak, the parameters are associated with a gaussian curve (3 parameters) located above a linear continuum (2 parameters). This method may produces the complete result of the calculation of statistical uncertainties and an accuracy higher than others methods. (author) [pt

  16. Fragment Formula Calculator (FFC): Determination of Chemical Formulas for Fragment Ions in Mass Spectrometric Data

    Science.gov (United States)

    Wegner, André; Weindl, Daniel; Jäger, Christian; Sapcariu, Sean C.; Dong, Xiangyi; Stephanopoulos, Gregory; Hiller, Karsten

    2015-01-01

    The accurate determination of mass isotopomer distributions (MID) is of great significance for stable isotope-labeling experiments. Most commonly, MIDs are derived from gas chromatography/electron ionization mass spectrometry (GC/EI-MS) measurements. The analysis of fragment ions formed during EI, which contain only specific parts of the original molecule can provide valuable information on the positional distribution of the label. The chemical formula of a fragment ion is usually applied to derive the correction matrix for accurate MID calculation. Hence, the correct assignment of chemical formulas to fragment ions is of crucial importance for correct MIDs. Moreover, the positional distribution of stable isotopes within a fragment ion is of high interest for stable isotope-assisted metabolomics techniques. For example, 13C-metabolic flux analyses (13C-MFA) are dependent on the exact knowledge of the number and position of retained carbon atoms of the unfragmented molecule. Fragment ions containing different carbon atoms are of special interest, since they can carry different flux information. However, the process of mass spectral fragmentation is complex, and identifying the substructures and chemical formulas for these fragment ions is nontrivial. For that reason, we developed an algorithm, based on a systematic bond cleavage, to determine chemical formulas and retained atoms for EI derived fragment ions. Here, we present the fragment formula calculator (FFC) algorithm that can calculate chemical formulas for fragment ions where the chemical bonding (e.g., Lewis structures) of the intact molecule is known. The proposed algorithm is able to cope with general molecular rearrangement reactions occurring during EI in GC/MS measurements. The FFC algorithm is able to integrate stable isotope labeling experiments into the analysis and can automatically exclude candidate formulas that do not fit the observed labeling patterns.1 We applied the FFC algorithm to create a

  17. [Flame atomic absorption spectrometric determination of H2O2 using (Au) core (Ag) shell nanoparticles].

    Science.gov (United States)

    Jiang, Zhi-Liang; Tang, Ya-Fang; Liang, Ai-Huiz; Gong, Qi

    2009-07-01

    The 10 nm gold nanoparticles were prepared by Frens procedure. Using tri-sodium citrate as reducer of AgNO3, and 10 nm gold nanoparticles as seed, the (Au)core(Ag)shell nanoparticles the size of about 30 nm were prepared at 90 degrees C for 10 min. Then it was separated by centrifuge at 10000 r x min(-1) for 15 min to obtain pure (Au)core(Ag)shell nanoparticles. In pH 3.8 sodium acetate-acetic acid buffer solution, hydroxyl free radical from Fenton reaction between Fe(II)-H2O2 oxidized (Au)core(Ag)shell nanoparticles to form silver ions. The silver ions in the centrifugal solutions can be measured by flame atomic absorption spectrometry at 328.1 nm. The silver ions in the centrifugal solutions increased with the H2O2 concentration increasing, and the absorption value at 328. 1 nm was enhanced linearly. The influence factors such as pH value, buffer solution volume, concentration of (Au)core(Ag)shell and Fe(II), reaction temperature and time, and centrifuging velocity and time were considered, respectively. Under the conditions of 0.20 mL pH 3.8 sodium acetate-acetic acid buffer solution, 50 microL of 2.0 mmol x L(-1) FeSO4, 60 microL of 2.94 x 10(-4) mol x L(-1) (Au)core(Ag)shell nanoparticle solution, reaction time of 20 min at 60 degrees C, and centrifugalization at 14 000 rpm for 10 min, the increased value deltaA is proportional to the H2O2 concentration (c) from 2. 64 to 42.24 micromol x L(-1), with a detection limit of 0.81 micromol x L(-1). The regress equation was deltaA = 0.014c-0.013 1, with a coefficient of 0.998 4. The effect of foreign substances such as 100-times glucose, Cu2+, Mg2+, Ca2+, 50-times urea, bovine serum albumin, Mn2+, Pb2+, and 30-times Cr3+ on the determination of 13.2 micromol x L(-1) H2O2 was examined respectively, with a relative error of +/- 10%. Results showed that there was no interference. This assay showed high sensitivity and good selectivity for quantitative determination of H2O2 in waste water samples, with satisfactory

  18. Determination of long-lived radionuclides at ultratrace level using advanced mass spectrometric techniques

    International Nuclear Information System (INIS)

    Zoriy, M.

    2005-11-01

    Determination of long-lived radionuclides at sub-fg concentration level is a challenging task in analytical chemistry. Inductively coupled plasma mass spectrometry (ICP-MS) with its ability to provide the sensitive and fast multielemental analysis is one of the most suitable method for the measurements of long lived radionuclides in the trace and ultra trace concentration range. In present the Ph.D. study a variety of procedures have been developed permitting the sub fg ml-1 determination of long-lived radionuclides (e.g. U, Th, Pu) as well as 226 Ra (T 1/2 = 1600 y) and 90 Sr (T 1/2 = 28.1 y) in different samples. In order to avoid isobaric interferences, to increase the sensitivity, precision and accuracy of the methods the application of different techniques: pre-concentration of the sample, off-line separation on the crown resin, measurements under cold plasma conditions, using microconcentric nebulizers (e.g DIHEN, DS-5) or the application of LA-ICP-MS for sample introduction have been studied. The limits of detection for different radionuclides was significantly improved in comparison to the ones reported in the literature, and, depending on the method applied, was varied from 10 -15 to 10 -18 g ml -1 concentration range. In addition to the analysis of long lived radionuclides, some other elements, that can present potential interest to the analyzed sample, were measured within the framework of the present study. Laser ablation inductively coupled plasma mass spectrometry (LAICP- MS) was used to produce images of element distribution in 20μm m thin sections of human brain tissue. The sample surface was scanned (raster area ∝80 mm 2 ) with a focused laser beam (wavelength 213 nm, diameter of laser crater 50μm, and laser power density 3x10 9 W cm -2 ) in a cooled laser ablation chamber developed for these measurements. Cross sections of human brain samples - hippocampus as well as brain tissues infected and non-infected with Glioblastoma Multiforme (tumor

  19. Fragment formula calculator (FFC): determination of chemical formulas for fragment ions in mass spectrometric data.

    Science.gov (United States)

    Wegner, André; Weindl, Daniel; Jäger, Christian; Sapcariu, Sean C; Dong, Xiangyi; Stephanopoulos, Gregory; Hiller, Karsten

    2014-02-18

    The accurate determination of mass isotopomer distributions (MID) is of great significance for stable isotope-labeling experiments. Most commonly, MIDs are derived from gas chromatography/electron ionization mass spectrometry (GC/EI-MS) measurements. The analysis of fragment ions formed during EI, which contain only specific parts of the original molecule can provide valuable information on the positional distribution of the label. The chemical formula of a fragment ion is usually applied to derive the correction matrix for accurate MID calculation. Hence, the correct assignment of chemical formulas to fragment ions is of crucial importance for correct MIDs. Moreover, the positional distribution of stable isotopes within a fragment ion is of high interest for stable isotope-assisted metabolomics techniques. For example, (13)C-metabolic flux analyses ((13)C-MFA) are dependent on the exact knowledge of the number and position of retained carbon atoms of the unfragmented molecule. Fragment ions containing different carbon atoms are of special interest, since they can carry different flux information. However, the process of mass spectral fragmentation is complex, and identifying the substructures and chemical formulas for these fragment ions is nontrivial. For that reason, we developed an algorithm, based on a systematic bond cleavage, to determine chemical formulas and retained atoms for EI derived fragment ions. Here, we present the fragment formula calculator (FFC) algorithm that can calculate chemical formulas for fragment ions where the chemical bonding (e.g., Lewis structures) of the intact molecule is known. The proposed algorithm is able to cope with general molecular rearrangement reactions occurring during EI in GC/MS measurements. The FFC algorithm is able to integrate stable isotope labeling experiments into the analysis and can automatically exclude candidate formulas that do not fit the observed labeling patterns.1 We applied the FFC algorithm to create

  20. Separation methods for radiometric and mass-spectrometric (ICP-MS) determination of technetium

    International Nuclear Information System (INIS)

    Bartosova, A.

    2005-01-01

    Declaration of specific activities of important radionuclides arisen by liquidation low-level nuclear waste represents an actual problem by decommissioning of NPP Jaslovske Bohunice. 99 Tc is an anthropological, long term half life radionuclide and belongs to the significant beta emitter with the influence on the radionuclides composition of the radwastes produced in NPP A-1 Jaslovske Bohunice. 99 Tc was determined in samples of soils, solid and liquid radioactive wastes from NPP Jaslovske Bohunice. 1. Several sorbents for Tc-99 separation were prepared. The prepared extraction materials were based on: Aliquat-336/ Polymer 7K1195, Aliquat-336/Teflon, Aliquat-336/hydrophobized silica gel with different concentrations of anchored quaternary amine (Aliquat-336), TOA/silica gel and TOA/Teflon. Prepared sorbents anchored on Teflon and polymer were not suitable as chromatographic bed material because of their non porously surface. Prepared sorbents based on TOA/Teflon Alq./ Teflon were viscously in the concentration range of amines (30%-60%), in concentration in the range (10%-20%) were amines sorbed with low yields - bounded Aliquat-336 on the prepared sorbent were about 4%-18%. It was found out: - By Tc desorption using prepared sorbents based on Aliquat-336/Polymer 7K1195 and Aliquat-336/Teflon were not reached satisfying recoveries - Organic phase - TOA was eluted with 99 mTcO 4 - by Tc desorption using sorbents TOA/silica gel and TOA/Teflon. 2. The best for effective separation of Tc-99 was found out the chromatographic material based on Aliquat-336 and hydrophobized silica gel. The highest retention of pertechnate was obtained in 0.1 mol.dm -3 HNO 3 media - chemical recovery of the sorption was nearly 100%. The elution of 99 mTcO 4 - was also tested with nitric acid concentration in the range 0.1-8 mol.dm -3 . The highest yields were using 20 ml of 8 mol.dm -3 HNO 3 - R=96.4%. The highest K D value of 99m TcO 4 - 2778 ml.g -1 were obtained in 0.1 mol. dm -3 HNO 3

  1. Honeybee Venom Proteome Profile of Queens and Winter Bees as Determined by a Mass Spectrometric Approach

    Science.gov (United States)

    Danneels, Ellen L.; Van Vaerenbergh, Matthias; Debyser, Griet; Devreese, Bart; de Graaf, Dirk C.

    2015-01-01

    Venoms of invertebrates contain an enormous diversity of proteins, peptides, and other classes of substances. Insect venoms are characterized by a large interspecific variation resulting in extended lists of venom compounds. The venom composition of several hymenopterans also shows different intraspecific variation. For instance, venom from different honeybee castes, more specifically queens and workers, shows quantitative and qualitative variation, while the environment, like seasonal changes, also proves to be an important factor. The present study aimed at an in-depth analysis of the intraspecific variation in the honeybee venom proteome. In summer workers, the recent list of venom proteins resulted from merging combinatorial peptide ligand library sample pretreatment and targeted tandem mass spectrometry realized with a Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS/MS). Now, the same technique was used to determine the venom proteome of queens and winter bees, enabling us to compare it with that of summer bees. In total, 34 putative venom toxins were found, of which two were never described in honeybee venoms before. Venom from winter workers did not contain toxins that were not present in queens or summer workers, while winter worker venom lacked the allergen Api m 12, also known as vitellogenin. Venom from queen bees, on the other hand, was lacking six of the 34 venom toxins compared to worker bees, while it contained two new venom toxins, in particularly serine proteinase stubble and antithrombin-III. Although people are hardly stung by honeybees during winter or by queen bees, these newly identified toxins should be taken into account in the characterization of a putative allergic response against Apis mellifera stings. PMID:26529016

  2. Honeybee venom proteome profile of queens and winter bees as determined by a mass spectrometric approach.

    Science.gov (United States)

    Danneels, Ellen L; Van Vaerenbergh, Matthias; Debyser, Griet; Devreese, Bart; de Graaf, Dirk C

    2015-10-30

    Venoms of invertebrates contain an enormous diversity of proteins, peptides, and other classes of substances. Insect venoms are characterized by a large interspecific variation resulting in extended lists of venom compounds. The venom composition of several hymenopterans also shows different intraspecific variation. For instance, venom from different honeybee castes, more specifically queens and workers, shows quantitative and qualitative variation, while the environment, like seasonal changes, also proves to be an important factor. The present study aimed at an in-depth analysis of the intraspecific variation in the honeybee venom proteome. In summer workers, the recent list of venom proteins resulted from merging combinatorial peptide ligand library sample pretreatment and targeted tandem mass spectrometry realized with a Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS/MS). Now, the same technique was used to determine the venom proteome of queens and winter bees, enabling us to compare it with that of summer bees. In total, 34 putative venom toxins were found, of which two were never described in honeybee venoms before. Venom from winter workers did not contain toxins that were not present in queens or summer workers, while winter worker venom lacked the allergen Api m 12, also known as vitellogenin. Venom from queen bees, on the other hand, was lacking six of the 34 venom toxins compared to worker bees, while it contained two new venom toxins, in particularly serine proteinase stubble and antithrombin-III. Although people are hardly stung by honeybees during winter or by queen bees, these newly identified toxins should be taken into account in the characterization of a putative allergic response against Apis mellifera stings.

  3. Liquid Chromatography-Tandem Mass Spectrometric Assay for Determination of Stavudine in Human Plasma

    Directory of Open Access Journals (Sweden)

    Fengdan Jin

    2014-01-01

    Full Text Available A LC-MS/MS method for determination of stavudine in human plasma was established and validated, and it was applied to the pharmaceutical formulations bioequivalence study. 0.5 mL plasma sample was extracted by liquid-liquid extraction. Stavudine was detected by a LC-MS/MS system. The pharmacokinetic parameters of stavudine in different formulations were calculated by noncompartment model statistics. The method was linear over the concentration ranges 5.00–1000 ng/mL in plasma. The intra- and interassay relative standard deviation (RSD was <10%. The average accuracies for the assay at three concentrations (5.00, 80.0, and 900 ng/mL were from 100.2% to 102.5%. Pharmacokinetic parameters of stavudine reference formulation were obtained as follows: Tmax was 0.6±0.2 h, Cmax was 480.7±150.9 g/L, t1/2 was 1.7±0.4 h, and AUC0-t was 872.8±227.8 g·h/L, and pharmacokinetic parameters of stavudine test formulation were obtained as follows: Tmax was 0.5±0.2 h, Cmax was 537.5±178.5 g/L, t1/2 was 1.7±0.3 h, and AUC0-t was (914.1±284.5 g·h/L. Calculated with AUC0-t, the bioavailability of two formulations was 105.0%.

  4. Determination of Glomerular Filtration Rate by Using Gamma camera

    International Nuclear Information System (INIS)

    Amer, M.; Salim, D.

    2007-01-01

    Glomerular filtration rate (GFR) is a commonly accepted standard measure of renal function. It is routinely measured using tracers that are cleared exclusively by glomerular filtration. The aim of this study was to apply new nuclear medicine technique based on direct determination of clearance of a radioactive tracer provided that all the uptake compartments of the radioactive tracer should be included in the field of the view of the gamma camera. A total of 10 men and 7 women range from 27 to 64 years old were studied using dual head gamma camera. The data for clearance calculation comprises : (1) a transmission scan of part of the body using water phantom with a uniform distribution of the radioisotope , (2) the background corrected activity curves in the anterior and posterior views over all uptake compartments following the injection of radioactive tracer, and (3) the activity of radioactive tracer in two blood samples drawn during the examination. The results for GFR above 30 ml min -1 , the regression line of GFR by using simplified multiple sample method versus GFR in gamma camera method were not significantly different from the line of identity. The reliability of the gamma camera method was about 16%, 12 % and 8% for GFR values of 30, 60 and 100 ml min-1. Therefore, the reliability of the gamma camera and the simplified multiple sample method for prediction of GFR were almost the same.

  5. Determination of the shielding factors for gamma-ray spectrometers

    International Nuclear Information System (INIS)

    Korun, M.; Vodenik, B.; Zorko, B.

    2014-01-01

    A method for determining the shielding factors for gamma-ray spectrometers is described. The shielding factors are expressed by decomposing the peaked background of the spectrometer into contributions of the detector, spectrometer shield and ambient radiation to the spectrometer background. The dimensions of the sample and its mass-attenuation coefficient are taken into account using a simple model. For six spectrometers, with contributions to the background quantified, the shielding factors were determined for the background based on the thorium decay series and the radon daughters. For a water sample with a diameter of 9 cm and a thickness of 4 cm and the nuclides of the thorium decay series that are in the spectrometer shields, the values of the shielding factors lie in the interval 0.95–1.00. For a spectrometer exhibiting the diffusion of radon into the shielding material, the values of the shielding factors for the same sample for gamma-rays from the radon daughters lie in the interval 0.88–1.00. - Highlights: • A model is described to assess shielding factors for gamma-ray spectrometers. • The background due to the detector, shield and ambient radiation must be known. • The sample attenuation, its dimensions and distance from the crystal are considered. • Shielding factors for gamma-rays from the 232 Th and 226 Ra decay chains are assessed. • For a water sample with a mass of 0.25 kg, shielding factors above 0.88 are obtained

  6. Spectrometric mixture analysis: An unexpected wrinkle

    Indian Academy of Sciences (India)

    The spectrometric analysis of a mixture of two chemically and spectroscopically similar compounds is illustrated for the simultaneous spectrometric determination of caffeine and theobromine, the primary stimulants in coffee and tea, based on their ultraviolet absorbances. Their analysis indicates that such measurements ...

  7. Development and application of mass spectrometric techniques for ultra-trace determination of236U in environmental samples-A review.

    Science.gov (United States)

    Bu, Wenting; Zheng, Jian; Ketterer, Michael E; Hu, Sheng; Uchida, Shigeo; Wang, Xiaolin

    2017-12-01

    Measurements of the long-lived radionuclide 236 U are an important endeavor, not only in nuclear safeguards work, but also in terms of using this emerging nuclide as a tracer in chemical oceanography, hydrology, and actinide sourcing. Depending on the properties of a sample and its neutron irradiation history, 236 U/ 238 U ratios from different sources vary significantly. Therefore, this ratio can be treated as an important fingerprint for radioactive source identification, and in particular, affords a definitive means of discriminating between naturally occurring U and specific types of anthropogenic U. The development of mass spectrometric techniques makes it possible to determine ultra-trace levels of 236 U in environmental samples. In this paper, we review the current status of mass spectrometric approaches for determination of 236 U in environmental samples. Various sample preparation methods are summarized and compared. The mass spectrometric techniques emphasized herein are thermal ionization mass spectrometry (TIMS), inductively coupled plasma mass spectrometry (ICP-MS) and accelerator mass spectrometry (AMS). The strategies or principles used by each technique for the analysis of 236 U are described. The performances of these techniques in terms of abundance sensitivity and detection limit are discussed in detail. To date, AMS exhibits the best capability for ultra-trace determinations of 236 U. The levels and behaviors of 236 U in various environmental media are summarized and discussed as well. Results suggest that 236 U has an important, emerging role as a tracer for geochemical studies. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Comparison of the precision and accuracy of digital versus analogue gamma-ray spectrometric systems used in INAA for evaluation of homogeneity and certification of reference materials of the IAEA

    International Nuclear Information System (INIS)

    Makarewicz, M.; Burns, K.

    2000-01-01

    Performance of three commercial gamma-ray spectrometric systems was evaluated for precision and accuracy prior to use in characterization of reference materials. Two of the systems were based on fast processing of the analogue signal from the amplifier (EGG Ortec model 672) using a loss free counting module (Canberra model LFC 599) interfaced to one of two analog-to-digital converters (Canberra models 8713 or 8715). The third system was based on a digital signal processor (Canberra model DSP 9660). Performance of the systems was tested over a range of count rates up to a maximum of 70,000 counts per second (dead time up to 90%) using 60 Co and 137 Cs sources. Best resolution was achieved with an analogue system with ADC 8713. The analytical results obtained with the digital system show the lowest and well-quantified uncertainty. (author)

  9. In-situ gamma spectrometry method for determination of environmental gamma dose

    International Nuclear Information System (INIS)

    Conti, Claudio de Carvalho

    1995-07-01

    This work tries to establish a methodology for germanium detectors calibration, normally used for in situ gamma ray spectrometry, for determining the environmental exposure rate in function of the energy of the incident photons. For this purpose a computer code has been developed, based on the stripping method, for the computational spectra analysis to calculate the contribution of the partial absorption of the gamma rays (Compton effect) in the active and nonactive parts of the detector. The resulting total absorption spectrum is then converted to fluence distribution in function of the energy for the photons reaching the detector, which is then used to calculate the exposure rate or kerma in air. The unfolding and fluency convention parameters are determined by detector calibration using point gamma sources. The method is validated by comparison of the results against the calculated exposure rate at a point of interest for the standards. This method is used for the direct measurement of the exposure rate distribution in function of the energy at the site, in situ measurement technic, leading to rapid results during an emergency situation and also used for indoor measurements. (author)

  10. Development and method of use of a mass spectrometric isotope dilution analysis within the use of negative thermoionisation for determination of boron traces

    International Nuclear Information System (INIS)

    Zeininger, H.

    1984-01-01

    A mass spectrometric trace boron determination using negative thermionisation was developed. It is based on the determination of the ratio of BO 2 - isotopes ( 10 B and 11 B). A high stability and a constant intensity at a given temperature of the BO 2 - ion currents allow for a computer controlled measurement with a programmed heating. The reproducibility lies at around 0,004-0,08%. The boron determination using Mels potentiometry with a BF 4 - -ion selective electrode was used as an analytical comparison method. The MS-IDA was first used on metal samples, such as Al, Zr, and steel. Later on the boron in reagents, biological material (milk powder, spinach, water plants) and water were determined. For this material-dependent hydrolysation and separation procedures were worked out. The MS-IDA in comparison to all other analytical methods used by other collaborators offers the greatest accuracy. (RB) [de

  11. A liquid chromatography-mass spectrometric method for the determination of oak moss allergens atranol and chloroatranol in perfumes

    DEFF Research Database (Denmark)

    Bossi, Rossana; Rastogi, Suresh Chandra; Bernard, Guillaume

    2004-01-01

    This paper describes a validated liquid chromatographic-tandem mass spectrometric method for quantitative analysis of the potential oak moss allergens atranol and chloroatranol in perfumes and similar products. The method employs LC-MS-MS with electrospray ionization (ESI) in negative mode...... of detection, 5.0 ng/mL and 2.4 ng/mL, respectively, for atranol and chloroatranol, achieved by this method allowed identification of these compounds at concentrations below those causing allergic skin reactions in oak-moss-sensitive patients. The recovery of chloratranol from spiked perfumes was 96+/-4%. Low...... recoveries (49+/-5%) were observed for atranol in spiked perfumes, indicating ion suppression caused by matrix components. The method has been applied to the analysis of 10 randomly selected perfumes and similar products....

  12. Polyclonal antibody to ovomucoid determination in gamma irradiated laying eggs

    International Nuclear Information System (INIS)

    Harder, Marcia N.C.; Arthur, Valter; Silva, Lucia C.A.S.; Lopes, Tatiana G.G.; Duarte, Keila M.R.; Canniatti-Brazaca, Solange G.; Savino, Vicente J.M.; Coelho, Antonio A.D.

    2009-01-01

    To determine allergenic food proteins, one of the most used tests is the immunoassays such as ELISA (enzyme linked immunosorbent assay), where the antibody recognizes the antigen and this connection is showed by an enzymatic system, in other words, optical density. The aim of this study was to determine the polyclonal antibody efficiency, produced in laboratory, to identify the presence the ovomucoid antigen in treated eggs by gamma irradiation for its inactivation. To evaluate the treatments, polyclonal antibody was produced in female rabbits immunized with bioconjugated ovomucoid. Was used Freund Complete Adjuvant at first immunization and PBS Buffer at four subsequently immunizations every fifteen days, plus a booster 48 hours before the blood retreated. The blood serum was tittered by PTA-ELISA (Plate trapped antigen). All procedures were according to European Norms for ethical and animal welfare. It was used, in nature, commercial laying eggs. So the samples were submitted to the gamma radiation coming from a source of Co 60 , type Multipurpose, under a dose rate of 19.4 and 31.8 Gy/hour, in the doses: 0 (control); 10 KGy; 20 KGy and 30 KGy, in all rates. By the ELISA.s test we can find the egg allergen ovomucoid and the radiation treatment do not showed considerable changes. So we can concluded that the antibody produced is capable of identify the ovomucoid allergenic protein and the gamma irradiation in such rates does not shows changes in that protein, therefore showed some changes in the color and visual viscosity of the egg samples. (author)

  13. Decision Threshold and Detection Limit in Spectrometric Measurements. Part 1: Application to Gamma Spectrometry; Umbral de Decision y Limite de Deteccion en Medidas Espectrometricas. Parte 1: Aplicacion a la Espectrometria Gamma

    Energy Technology Data Exchange (ETDEWEB)

    Perez, C.; Gasco, C.; Lopez, M.A.

    2010-03-03

    This report summarised the author's lecture of the advanced gamma spectrometry course organised by CIEMAT. The characteristic limits determination in gamma spectrometry generally is obtained through the programming that the trade marks offers to the client with the objective of the automatic calculation of the activity concentrations existing in a sample. In this report, the examples shown in the ISO 11929 standard are compared to the programming realised by Genie 2k for determining characteristic limits. The main difference of both is located in the uncertainty calculations due to the efficiency calibration that is considered by ISO and not by Genie 2K. Through implementation in the software developed by trade marks will be possible to introduce this uncertainty and to assimilate to the calculation done by ISO 11929. In the second part of this report will be analyzed the more complicated samples of this application as counting in a whole body counter (following ISO-28218 about Performance Criteria for radio bioassay), multiplet, overlapping, addition of several peaks for obtaining the activity concentration, etc. (Author) 19 refs.

  14. A new method for the determination of radionuclide distribution in the soil by in situ gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Zombori, P.; Andrasi, A.; Nemeth, I.

    1995-01-01

    In case of major nuclear accidents when larger amount of radioactive material is released into the atmosphere vast areas can become contaminated by the nuclear fallout. The deposited radioactivity penetrates the soil in a complex manner: dry and wet deposition lead to different initial distribution patterns which are further modified by the later transport processes in the upper layers of the soil. The distribution is influenced by various factors (physico-chemical characteristics of the radioisotopes, soil type, weather conditions, environment etc.), the resulting soil profile is hardly predictable. An important lesson we learned from the Chernobyl reactor accident is the great variability of the contamination both in the extent of the deposition and in the penetration features. In recent years - following the reactor accident in Chernobyl - an increased interest for rapid methods of monitoring environmental radioactivity was expressed. The International Atomic Energy Agency initiated a research project to co-ordinate the activities carried out in various laboratories aiming at the development of rapid monitoring procedures. The Co-ordinated Research Project (CRP) G6 10 01 under the title Rapid Instrumental and Separation Methods for Monitoring Radionuclides in Food and the Environment has given a frame for 11 research programs. The Health Physics Department of the KFKI Institute for Atomic Energy Research (the former Central Research Institute for Physics) has taken a part in this CRP with a project titled: Rapid In Situ Gamma Spectrometric Determination of Fallout Radioactivity in the Environment. The main objective of our study was to find a method to estimate the penetration characteristics of the fallout radioactivity by using only spectral information obtained by the in situ spectrometric measurement thus avoiding the need for a long and tiresome sampling and sample analysis procedure

  15. Determination of the measurement threshold in gamma-ray spectrometry.

    Science.gov (United States)

    Korun, M; Vodenik, B; Zorko, B

    2017-03-01

    In gamma-ray spectrometry the measurement threshold describes the lover boundary of the interval of peak areas originating in the response of the spectrometer to gamma-rays from the sample measured. In this sense it presents a generalization of the net indication corresponding to the decision threshold, which is the measurement threshold at the quantity value zero for a predetermined probability for making errors of the first kind. Measurement thresholds were determined for peaks appearing in the spectra of radon daughters 214 Pb and 214 Bi by measuring the spectrum 35 times under repeatable conditions. For the calculation of the measurement threshold the probability for detection of the peaks and the mean relative uncertainty of the peak area were used. The relative measurement thresholds, the ratios between the measurement threshold and the mean peak area uncertainty, were determined for 54 peaks where the probability for detection varied between some percent and about 95% and the relative peak area uncertainty between 30% and 80%. The relative measurement thresholds vary considerably from peak to peak, although the nominal value of the sensitivity parameter defining the sensitivity for locating peaks was equal for all peaks. At the value of the sensitivity parameter used, the peak analysis does not locate peaks corresponding to the decision threshold with the probability in excess of 50%. This implies that peaks in the spectrum may not be located, although the true value of the measurand exceeds the decision threshold. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Vis-NIR spectrometric determination of Brix and sucrose in sugar production samples using kernel partial least squares with interval selection based on the successive projections algorithm.

    Science.gov (United States)

    de Almeida, Valber Elias; de Araújo Gomes, Adriano; de Sousa Fernandes, David Douglas; Goicoechea, Héctor Casimiro; Galvão, Roberto Kawakami Harrop; Araújo, Mario Cesar Ugulino

    2018-05-01

    This paper proposes a new variable selection method for nonlinear multivariate calibration, combining the Successive Projections Algorithm for interval selection (iSPA) with the Kernel Partial Least Squares (Kernel-PLS) modelling technique. The proposed iSPA-Kernel-PLS algorithm is employed in a case study involving a Vis-NIR spectrometric dataset with complex nonlinear features. The analytical problem consists of determining Brix and sucrose content in samples from a sugar production system, on the basis of transflectance spectra. As compared to full-spectrum Kernel-PLS, the iSPA-Kernel-PLS models involve a smaller number of variables and display statistically significant superiority in terms of accuracy and/or bias in the predictions. Published by Elsevier B.V.

  17. Gas chromatographic determination of pesticides in vegetable samples by sequential positive and negative chemical ionization and tandem mass spectrometric fragmentation using an ion trap analyser.

    Science.gov (United States)

    Hernando, M D; Agüera, A; Fernández-Alba, A R; Piedra, L; Contreras, M

    2001-01-01

    A selective and sensitive chromatographic method is described for the determination of nine organochlorine and organophosphorus pesticides in vegetable samples by gas chromatography-mass spectrometry. The proposed method combines the use of positive and negative chemical ionisation and tandem mass spectrometric fragmentation, resulting in a significant increase in selectivity and allowing the simultaneous confirmation and quantification of trace levels of pesticides in complex vegetable matrices. Parameters relative to ionisation and fragmentation processes were optimised to obtain maximum sensitivity. Repeatability and reproducibility studies yielded relative standard deviations lower than 25% in all cases. Identification criteria, such as retention time and relative abundance of characteristic product ions, were also evaluated in order to guarantee the correct identification of the target compounds. The method was applied to real vegetable samples to demonstrate its use in routine analysis.

  18. Determination of plutonium isotopes (238Pu, 239Pu, 240Pu, 241Pu) in environmental samples using radiochemical separation combined with radiometric and mass spectrometric measurements

    DEFF Research Database (Denmark)

    Xu, Yihong; Qiao, Jixin; Hou, Xiaolin

    2014-01-01

    This paper reports an analytical method for the determination of plutonium isotopes (238Pu, 239Pu, 240Pu, 241Pu) in environmental samples using anion exchange chromatography in combination with extraction chromatography for chemical separation of Pu. Both radiometric methods (liquid scintillation......, this is critical for the measurement of plutonium isotopes using mass spectrometric technique. Although the chemical yield of Pu in the entire procedure is about 55%, the analytical results of IAEA soil 6 and IAEA-367 in this work are in a good agreement with the values reported in the literature or reference...... counting and alpha spectrometry) and inductively coupled plasma mass spectrometry (ICP-MS) were applied for the measurement of plutonium isotopes. The decontamination factors for uranium were significantly improved up to 7.5×105 for 20 g soil compared to the level reported in the literature...

  19. Analytical laboratories method No. 4001 - automatic determination of U-235 wt% in a uranium matrix by gamma spectrometry

    International Nuclear Information System (INIS)

    1987-01-01

    This method is designed to automatically measure the U-235 concentration of various uranium-containing matrices (e.g., UO 3 , UF 4 , U 3 O 8 , sump samples, UNH, residues, etc.). Analyses are performed using a computer controlled sample changer. The technique is applicable to samples ranging from 0.20 to 20.0 wt% U-235. A complete gamma spectrometric U-235 analysis can be performed in two hours, or less

  20. Gamma-spectrometric surveys in differentiated granites. II: the Joaquim Murtinho Granite in the Cunhaporanga Granitic Complex, Parana, SE Brazil; Levantamentos gamaespectrometricos em granitos diferenciados. II: O exemplo do Granito Joaquim Murtinho, Complexo Granitico Cunhaporanga, Parana

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Francisco Jose Fonseca [Universidade Federal do Parana (UFPR), Curitiba, PR (Brazil). Dept. de Geologia. Lab. de Pesquisas em Geofisica Aplicada; Fruchting, Allan [Votorantim Metais, Sao Paulo, SP (Brazil)], e-mail: allan.fruchting@vmetais.com.br; Guimaraes, Gilson Burigo [Universidade Estadual de Ponta Grossa (UEPG), PR (Brazil). Dept. de Geociencias], e-mail: gburigo@ig.com.br; Alves, Luizemara Soares [PETROBRAS S.A., Rio de Janeiro, RJ (Brazil)], e-mail: luizemara@petrobras.com.br; Martin, Victor Miguel Oliveira; Ulbrich, Horstpeter Herberto Gustavo Jose [Universidade de Sao Paulo (USP), SP (Brazil). Inst. de Geociencias. Dept. de Mineralogia e Geotectonica], e-mail: vicmartin6@ig.com.br, e-mail: hulbrich@usp.br

    2009-07-01

    Detailed mapping at the NW corner of the large Neo proterozoic Cunhaporanga Granitic Complex (CGC), Parana state, SE Brazil, redefined the Joaquim Murtinho Granite (JMG), a late intrusion in CGC with an exposed area of about 10 km{sup 2}, made up mainly by evolved 'alaskites' (alkali-feldspar leuco granites). This unit is in tectonic contact with the Neoproterozoic-Eocambrian volcano-sedimentary Castro Group, to the W, and is intrusive into other less evolved granitic units of the CGC to the E. Petrographically, JMG shows mainly mesoperthite and quartz, with subordinate amounts of altered micas and some accessory phases, mainly zircon. The equi to inequigranular granites are usually deformed with cataclastic textures, are often brecciated, and may have miarolitic structures. Formation of late albite, sericite, carbonate and hematite was caused by deuteric and hydrothermal alteration. A gamma-ray spectrometric survey at 231 stations which measured total counts (TC), Ueq K%, eU ppm and eTh ppm was used to construct several direct and derived maps. Compared to neighboring units the JMG has significant anomalies, especially in the TC, %K, eTh and eU maps, although the differences are less obvious in some derived maps. These evolved granites are enriched in these three elements. Geochemical behavior of K, Th and U is used to analyse the results observed in maps. Enhanced weathering under a subtropical climate with moderate to high average temperatures and heavy rainfall affects mainly feldspars and biotite, and may also destabilize most U and Th-bearing accessory phases. Th is most likely retained in restite minerals in soils, being relatively immobile, while part of U may migrate as uranyl ion in oxidizing media. K is especially affected by feldspar alteration to K-free clays (mainly kaolinite), and may be completely leached. Gamma-ray spectrometric methods are valid tools to study facies in granitic rocks, especially in those that are enriched in K, Th and U

  1. A liquid chromatography-mass spectrometric method for the determination of oak moss allergens atranol and chloroatranol in perfumes.

    Science.gov (United States)

    Bossi, Rossana; Rastogi, Suresh C; Bernard, Guillaume; Gimenez-Arnau, Elena; Johansen, Jeanne D; Lepoittevin, Jean-Pierre; Menné, Torkil

    2004-05-01

    This paper describes a validated liquid chromatographic-tandem mass spectrometric method for quantitative analysis of the potential oak moss allergens atranol and chloroatranol in perfumes and similar products. The method employs LC-MS-MS with electrospray ionization (ESI) in negative mode. The compounds are analysed by selective reaction monitoring (SRM) of 2 or 3 ions for each compound in order to obtain high selectivity and sensitivity. The method has been validated for the following parameters: linearity; repeatability; recovery; limit of detection; and limit of quantification. The limits of detection, 5.0 ng/mL and 2.4 ng/mL, respectively, for atranol and chloroatranol, achieved by this method allowed identification of these compounds at concentrations below those causing allergic skin reactions in oak-moss-sensitive patients. The recovery of chloratranol from spiked perfumes was 96+/-4%. Low recoveries (49+/-5%) were observed for atranol in spiked perfumes, indicating ion suppression caused by matrix components. The method has been applied to the analysis of 10 randomly selected perfumes and similar products.

  2. A mass spectrometric method for diagnosis of gastrointestinal infections by 13 C determination from respiratory CO2

    International Nuclear Information System (INIS)

    Cuna, Stela; Ursu, D.; Cuna, C.; Berdea, P.; Sparchez, Z.

    2000-01-01

    The use of stable carbon isotopes in metabolic research on humans and large animals is expanding rapidly due to the increasing variety of labelled compounds, greater availability of analytical facilities, and absence of health risk from radiation.This study is focused on a new mass spectrometric technique to diagnose Helicobacter pylori (HP) infection of the gastric mucosa which results in ulcers and some forms of gastric cancer. The method is based on measuring 13 C-enrichment in exhaled air by isotope ratios mass spectrometry. In this breath test, 13 C-labelled urea is given orally to the patient. If HP is present, the 13 C-urea is decomposed rapidly by these bacteria to 13 CO 2 which circulates to the lungs and is expelled in the breath where it can be detected. The protocol of the method is described and one example of the use of 13 C-urea is presented. The 13 C-enrichment in CO 2 exhaled is measured by mass spectrometry with double collector and the results are expressed in relative delta (δ) per mil ( o / oo ) units. The instrumental precision was ± 0.12 o / oo . The δ 13 C was measured in both pre and post - dose breath samples collected from infected patient at 20, 40 and 60 min post-dose. The results showed 13 C increases of > 25 o / oo at 40 min, in good agreement with the data of literature. We concluded that these breath tests are ideally suited to diagnose HP infection as a nonradioactive, noninvasive and applicable to subjects of any population method. (authors)

  3. Determination of gamma-ray-induced displacement rates

    International Nuclear Information System (INIS)

    Gold, R.; Doran, D.G.; Roberts, J.H.

    1989-01-01

    To define the gamma-ray component of the radiation field in light water reactor (LWR) pressure vessel (PV) environments, gamma-ray spectrometry experiments were conducted in the low power PV mockup at the poolside critical assembly (PCA) at the Oak Ridge National Laboratory (ORNL). Gamma-ray displacement rates can be calculated directly from absolute electron spectra observed with the Janus probe gamma-ray spectrometry. Gamma-ray displacement results are presented for the 1/4-T, 1/2-T, and 3/4-T locations of the 12/13 and 4/12 simulated surveillance capsule (SSC) configurations. In addition, the gamma-ray displacement rate at the SSC location was inferred using thermoluminescent dosimeter (TLD) gamma-ray dosimetry results obtained in the 4/12 SSC configuration at the PCA. Compared with neutron-induced displacement rates, the calculated gamma-ray-induced displacement rates are small at all these LWR-PV locations. The ratio of gamma-ray-induced to neutron-induced displacement rates never exceeds roughly 5 X 10 -3

  4. NASVD and MNF techniques and your application noise reduction in gamma-ray spectrometric data; As tecnicas NASVD e MNF e sua aplicacao na reducao de ruidos em dados gamaespectrometricos

    Energy Technology Data Exchange (ETDEWEB)

    Cavallaro, Francisco de Assis, E-mail: assisfc@yahoo.com.br, E-mail: assis@agp-la.org [Departamento de Geologia Sedimentar e Ambiental, DGSA, Instituto de Geociencias, IG, Universidade de Sao Paulo, SP (Brazil); AGPLA, AeroGeoPhysica Latinoamerica, Sao Paulo, SP (Brazil); Portugal, Rodrigo S.; Bizuti, Ariathemis M., E-mail: portugal@ige.unicamp.br, E-mail: ambizuti@ige.unicamp.br [Departamento de Geologia e Recursos Naturais, DGRN, Instituto de Geociencias, IG, Universidade Estadual de Campinas, SP (Brazil); Silva, Adalene M., E-mail: adalene@unb.br [Universidade de Brasilia (UnB), DF (Brazil). Inst. de Geociencias. Dept. de Geoquimica e Recursos Minerais (GRM)

    2009-04-15

    The radioactive decay is a random process, and the measurement precision is ruled by statistical laws. The counting ratios of the profiles are always noisy when analyzed for short periods, such as one second per measurement. Corrections made at the end of conventional processing in the airborne gamma-ray spectrometric method data are not enough to remove and minimize, or even reduce considerably, the spectrum's originated noise. Two statistic methods that act locally in collected data, in the spectrum domain, have been suggested by literature to remove such remaining noises, the Noise-Adjusted Singular Value Decomposition - NASVD and Maximum Noise Fraction - MNF. These methods produce a significantly noise reduction. In this work both methods were applied in an area comprehended by two blocks, I and II, of the airborne survey that covers the west area of Mineral Province of Tapajos between Para and Amazon states. The filtered and non-filtered data with the NASVD and MNF techniques were processed with the Lasa's parameters. The comparison of results between maps and profiles shows that both methods are valuable, since there was resolution gain in these products. (author)

  5. Spectrometric techniques 4

    CERN Document Server

    Vanasse, George A

    2013-01-01

    Spectrometric Techniques, Volume IV discusses three widely diversified areas of spectrometric techniques. The book focuses on three spectrometric methods. Chapter 1 discusses the phenomenology and applications of Coherent Anti-Stokes Raman Spectroscopy (CARS), the most commonly used optical technique that exploit the Raman effect. The second chapter is concerned with diffraction gratings and mountings for the Vacuum Ultraviolet Spectral Region. Chapter 3 accounts the uses of mass spectrometry, detectors, types of spectrometers, and ion sources. Physicists and chemists will find the book a go

  6. Determination of gamma ray attenuation coefficients of Al–4% Cu ...

    Indian Academy of Sciences (India)

    Gamma ray attenuation coefficients of metal matrix composites have been investigated. For this purpose, the linear attenuation coefficients of composites containing boron carbide (B4C) at different rates have been measured using a gamma spectrometer that contains a NaI(Tl) detector and MCA at 662, 1173 and 1332 keV, ...

  7. Determination of gamma ray attenuation coefficients of Al–4% Cu ...

    Indian Academy of Sciences (India)

    Administrator

    Abstract. Gamma ray attenuation coefficients of metal matrix composites have been investigated. For this purpose, the linear attenuation coefficients of composites containing boron carbide (B4C) at different rates have been measured using a gamma spectrometer that contains a NaI(Tl) detector and MCA at 662, 1173 and.

  8. Spectrometric assembly for portable installations

    International Nuclear Information System (INIS)

    Kluger, A.; Popescu, C.

    1997-01-01

    The components of the portable spectrometric assembly are: - the detecting probe with Na I(Tl) crystal and air-tight case of industrial type; - a microcomputer; - a unit of analogical processing of the signal from the detecting probe; - a single-channel analyzer with adjustable threshold; - commands and display module; - a source of high voltage; - an electrical supply battery. The device uses the method of gamma photons detection in energetic windows. Through theoretical and experimental studies carried out during the prototype development phase, the superiority of this method has been proved as compared with the installations which make use of the classical principle of photon integral detection. The achieved prototype has a basic program enabling the setting of all working parameters (measuring time, discriminating thresholds, discriminators operating conditions, etc.). Through the included interface RS232 it is possible to transmit the data to a more powerful computer in order to continually process the results. The spectrometric assembly, realized on the basis of micro-computers, can be used in a wide range of applications: measurement of thickness and erosion of walls and tubes, measurement of level in closed containers, of soil density, etc. The adjustment for specific application is performed only through a program modification. (authors)

  9. Performance test of Spectran-F and Spectran-III computer programs for resolving the 137Cs-110Ag double peak in gamma-ray spectrometric analysis

    International Nuclear Information System (INIS)

    Terada, H.; Malinowski, J.; Blick, H.

    1981-09-01

    The performance of the computer programs (Spectran F and Spectran-III) in resolving the 137 Cs-sup(110m)Ag double peak at 661.6-657.7 keV in the gamma-ray spectrum was investigated. In the experiments, the intensity ratios of both lines in the double peak were varied from 0.1 to 60. The results obtained show, that both programs have almost the same performance in resolving the double peak investigated, with slight superiority of Spectran-F. If accuracy better than 5% is desired, the peak intensity ratio in the dublet must be kept below 10. (orig.)

  10. A Critical Look at $\\gamma$ Determinations from $B\\rightarrow \\pi K$ Decays

    CERN Document Server

    Fleischer, Robert

    2000-01-01

    The determination of the angle $\\gamma$ of the unitarity triangle of the CKM matrix is a challenge for the $B$-factories. In this context, $B\\to\\pi K$ decays received a lot of attention, providing various interesting ways to constrain and determine $\\gamma$. These strategies are briefly reviewed, and their virtues and weaknesses are compared with one another.

  11. Identification of boiler tube leak in PHWR by measuring short lived radioisotope Iodine-134 in boiler water using gamma spectrometric techniques

    International Nuclear Information System (INIS)

    Pal, P.K.; Bohra, R.C.

    2015-01-01

    The boiler tube made up of Monel-400 of RAPS-2 has failed on few occasions. Due to the failure of boiler tube, the active heavy water enters into boiler and feed water leading to contamination of radioactivity in secondary water circuit. The identification of boiler tube failure was done by measuring gamma ray activity of Iodine-134 in the boiler water with sample using gamma spectrometry with high purity germanium detector. In order to increase the sensitivity of the method 5 liters of Boiler water sample was passed through a plastic column containing 40 ml of anion resin and 10 ml of activated charcoal to capture the isotopes of Iodine in the anionic form and molecular form. Samples were collected from all 8 Boilers of RAPS-2. The activity of 134 I was shown only by Boiler - 5. No other boilers showed any activity of 134 I. This indicated that Boiler - 5 had leaky tubes. The leaky hairpin of boiler - 5 was identified by measuring Tritium and IP in the riser and down comer of all 10 HXs. On the basis of Tritium and IP result, HX-7 was identified as leaky hairpin. (author)

  12. Ionic liquid-linked dual magnetic microextraction of lead(II) from environmental samples prior to its micro-sampling flame atomic absorption spectrometric determination.

    Science.gov (United States)

    Yilmaz, Erkan; Soylak, Mustafa

    2013-11-15

    A novel and rapid microextraction approach termed as ionic liquid-linked dual magnetic microextraction (IL-DMME), was developed for the atomic absorption spectrometric determination of lead. The developed method based on a combination of dispersive liquid-liquid microextraction (DLLME) and dispersive micro solid-phase extraction (D-μ-SPE). In the first DLLME step, 1-butyl-3-methylimidazolium hexafluorophosphate [C4mim][PF6], was selected to extract the lead-pyrrolidine-dithiocarbamate (Pb-PDC) complex from sample solution by the assistance of vortex agitator. After the first step, fifty milligrams of Fe3O4 magnetic nanoparticles (MNPs) were added to extraction of the ionic liquid and Pb-PDC complex in aqueous solution. The effective factors in proposed IL-DMME procedure, including volume of 1-butyl-3-methylimidazolium hexafluorophosphate, amount of Fe3O4 magnetic nanoparticles, vortex time, amount of ammonium pyrrolidinedithiocarbamate, sample volume and matrix effect were optimized in details. Under the optimal conditions, the method present has low detection limit (0.57 μg L(-1)), high preconcentration factor (160) and good repeatability (analysis of the certified reference materials and addition-recovery tests. The method was successfully applied to the determination of lead in water, plant and hair samples. © 2013 Elsevier B.V. All rights reserved.

  13. Determination of gamma ray shielding parameters of rocks and concrete

    Science.gov (United States)

    Obaid, Shamsan S.; Gaikwad, Dhammajyot K.; Pawar, Pravina P.

    2018-03-01

    Gamma shielding parameters such as mass attenuation coefficient (μ/ρ), effective atomic number (Zeff) and electron density (Neff) have been measured and calculated for rocks and concrete in the energy range 122-1330 keV. The measurements have been carried out at 122, 356, 511, 662, 1170, 1275, 1330 keV gamma ray energies using a gamma spectrometer includes a NaI(Tl) scintillation detector and MCA card. The atomic and electronic cross sections have also been investigated. Experimental and calculated (WinXCom) values were compared, and good agreement has been observed within the experimental error. The obtained results showed that feldspathic basalt, compact basalt, volcanic rock, dolerite and pink granite are more efficient than the sandstone and concrete for gamma ray shielding applications.

  14. Determination of IRT-2M fuel burnup by gamma spectrometry.

    Science.gov (United States)

    Koleška, Michal; Viererbl, Ladislav; Marek, Milan; Ernest, Jaroslav; Šunka, Michal; Vinš, Miroslav

    2016-01-01

    A spectrometric system was developed for evaluating spent fuel in the LVR-15 research reactor, which employs highly enriched (36%) IRT-2M-type fuel. Such system allows the measurement of detailed fission product profiles. Within these measurements, nuclides such as (137)Cs, (134)Cs, (144)Ce, (106)Ru and (154)Eu may be detected in fuel assemblies with different cooling times varying between 1.67 and 7.53 years. Burnup calculations using the MCNPX Monte Carlo code data showed good agreement with measurements, though some discrepancies were observed in certain regions. These discrepancies are attributed to the evaluation of irradiation history, reactor regulation pattern and buildup schemes. Copyright © 2015 Elsevier Ltd. All rights reserved.

  15. Critical comparison of radiometric and mass spectrometric methods for the determination of radionuclides in environmental, biological and nuclear waste samples

    DEFF Research Database (Denmark)

    Hou, Xiaolin; Roos, Per

    2008-01-01

    spectrometry, and glow discharge mass spectrometry are reviewed for the determination of radionuclides. These methods are critically compared for the determination of long-lived radionuclides important for radiation protection, decommissioning of nuclear facilities, repository of nuclear waste, tracer...

  16. Direct injection liquid chromatography/electrospray ionization mass spectrometric horse urine analysis for the quantification and confirmation of threshold substances for doping control. II. Determination of theobromine.

    Science.gov (United States)

    Vonaparti, A; Lyris, E; Panderi, I; Koupparis, M; Georgakopoulos, C

    2009-04-01

    In equine sport, theobromine is prohibited with a threshold level of 2 microg mL(-1) in urine, hence doping control laboratories have to establish quantitative and qualitative methods for its determination. Two simple liquid chromatography/mass spectrometry (LC/MS) methods for the identification and quantification of theobromine were developed and validated using the same sample preparation procedure but different mass spectrometric systems: ion trap mass spectrometry (ITMS) and time-of-flight mass spectrometry (TOFMS). Particle-free diluted urine samples were directly injected into the LC/MS systems, avoiding the time-consuming extraction step. 3-Propylxanthine was used as the internal standard. The tested linear range was 0.75-15 microg mL(-1). Matrix effects were evaluated analyzing calibration curves in water and different fortified horse urine samples. A great variation in the signal of theobromine and the internal standard was observed in different matrices. To overcome matrix effects, a standard additions calibration method was applied. The relative standard deviations of intra- and inter-day analysis were lower than 8.6 and 7.2%, respectively, for the LC/ITMS method and lower than 5.7 and 5.8%, respectively, for the LC/TOFMS method. The bias was less than 8.7% for both methods. The methods were applied to two case samples, demonstrating simplicity, accuracy and selectivity. Copyright (c) 2009 John Wiley & Sons, Ltd.

  17. Methodology for determination of activity of radionuclides by gamma spectrometry

    International Nuclear Information System (INIS)

    Fragoso, Maria da Conceicao de Farias; Oliveira, Victor Rogerio S. de; Oliveira, Mercia L.; Lima, Fernando Roberto de Andrade

    2014-01-01

    Due to the growth in the number of procedures that make use of the positron emission tomography (PET), there is a need for standard solutions for the calibration of the systems used for the measurement of the PET radiopharmaceutical (activimeter) in radiopharmacies and in nuclear medicine services. Among the existing alternatives for the standardization of radioactive sources, the method known as gamma spectrometry is widely used for short-lived radionuclides. The purpose of this study was to implement the methodology for standardization of the 18 F solutions by gamma spectrometry at the Regional Center for Nuclear Sciences of the Northeast (CRCN-NE/CNEN-NE), Brazil. (author)

  18. Correction for sample self-absorption in activity determination by gamma spectrometry

    International Nuclear Information System (INIS)

    Galloway, R.B.

    1991-01-01

    Gamma ray spectrometry is a convenient method of determining the activity of the radioactive components in environmental samples. Commonly samples vary in gamma absorption or differ in absorption from the calibration standards available, so that accurate correction for self-absorption in the sample is essential. A versatile correction procedure is described. (orig.)

  19. Determination of gamma ray attenuation coefficients of Al–4% Cu ...

    Indian Academy of Sciences (India)

    Administrator

    in the present work, the γ-ray attenuation coefficients of. MMCs for different gamma energies (ranging from 662 to 1332 keV) by using different point radioactive sources. (137Cs and 60Co) have been investigated. The measured results have been compared with the calculation. 2. Experimental details. 2.1 Production of ...

  20. Determination of protein content in grains by radioactive thermal neutron capture prompt gamma rays analysis

    International Nuclear Information System (INIS)

    Carbonari, A.W.

    1983-01-01

    The radioactive thermal neutron capture prompt gamma rays technique can be used to determinate the nitrogen content in grains without chemical destruction, with good precision and relative rapidity. This determination is based on the detection of prompt gamma rays emitted by the 14 N(n,γ) 15 N reaction product. The samples has been irradiated the tanGencial tube of the IEA-R1 research reator and a pair spectrometer has been used for the detection of the prompt gamma rays. The nitrogen content is determinated in several samples of soybean, commonbean, peas and rice, and the results is compared with typical nitrogen content for each grain. (Autor) [pt

  1. Gamma-spectrometric surveys in differentiated granites. I: a review of the method and of the geochemical behavior of K, Th and U; Levantamentos gamaespectrometricos em granitos diferenciados. I: revisao da metodologia e do comportamento geoquimico dos elementos K, Th e U

    Energy Technology Data Exchange (ETDEWEB)

    Ulbrich, Horstpeter Herberto Gustavo Jose; Ulbrich, Mabel Norma Costas [Universidade de Sao Paulo (USP), SP (Brazil). Inst. de Geociencias. Dept. de Mineralogia e Geotectonica], e-mail: hulbrich@usp.br, e-mail: mulbrich@usp.br; Ferreira, Francisco Jose Fonseca [Universidade Federal do Parana (UFPR), Curitiba, PR (Brazil). Dept. de Geologia. Lab. de Pesquisas em Geofisica Aplicada; Alves, Luizemara Soares [PETROBRAS S.A., Rio de Janeiro, RJ (Brazil)], e-mail: luizemara@petrobras.com.br; Guimaraes, Gilson Burigo [Universidade Estadual de Ponta Grossa (UEPG), PR (Brazil). Dept. de Geociencias], e-mail: gburigo@ig.com.br; Fruchting, Allan [Votorantim Metais, Sao Paulo, SP (Brazil)], e-mail: allan.fruchting@vmetais.com.br

    2009-07-01

    This contribution is part of a research project on the Neo proterozoic Cunhaporanga Granitic Complex (CGC), cropping out in the Ponta Grossa Arch (Parana state, SE Brazil). An initial study used the gamma-spectrometric data of the Serra do Mar Sul Aero geophysical Project, performed during the 70's for CPRM. Later, terrestrial gamma-spectrometric surveys focused on the study of the differentiated Joaquim Murtinho Granite (JMG) in the NW corner of CGC, and the Serra do Carambei Granite, to the SW. In this paper, the results obtained for JMG are presented in two parts. The first deals with methodology and the presentation of several gamma-spectrometric 'color-scale' maps, indicating that results obtained in granites depend strongly on a climatic factor, given the mobility of K during weathering in subtropical climates with strong rainfalls, also favoring a greater mobility of U. Minerals that are U and Th hosts, documented in granites, are reviewed, together with the weathering processes that control the mobility of K, U and Th in soils. Strong K signals in granitic areas submitted to these climates document the presence of fresh rock and/or effects of hydrothermal alteration, while weak or nil signals are evidence of strong leaching of K during weathering. U and Th will be retained in the residual soils, in part leading to their selective enrichment, also coupled with soil migration to lower topographic levels by colluvial transport. The larger solubility of U (as uranyl ion) allows its liberation under oxidizing conditions, and its migration, limited by the possibility of absorption in newly formed mineral and organic soil phases. Th should be retained almost totally in resistant phases and, when liberated in solution, will mostly be fixed in organic and inorganic soil substances. (author)

  2. Determination of gamma radiation shielding characteristics of some tropical woods

    International Nuclear Information System (INIS)

    Aigbosuria, E. F.

    2011-01-01

    This study compares the shielding characteristics of twenty-two tropical woods by using gamma scintillation detection method. Woods sourced are Anogeisus Leiocarpus(Ayin), Nesogordonia Papverifera(Oro), Entandrophragma Microphyllum(Anunje), Brachystagia Eurycoma(Ako), Cassia Alata(Asunrun), Afzelia Africana(Apa-Igbo), Khaya Grandifoliala(Gedu), Piptadenistrum Africana(Agbonyin), Nanclea Diderrehii(Opepe), Khaya Ivorensis(Oganwo), Chlorophora Excelsa(Iroko), Masonia altissima(Odogi), Entandrophragma Angolense(Ijebo), Altium Sativum(Ayo), Albizia Zygia(Ayunre), Terminalia Superba(Afara), Cordia Millenii(Omo), Melania(Melania), Pycnanthus Angolensis(Akomu), Triplochitons Scleroxylon(Arere), Pine(Pine), Ceiba Pentradra(Araba). The intensities of the emergent radiation were measured, when each of these woods were placed between a scintillation detector and a standard radioactive source. Analysis of result obtained shows an appreciable evidence of radiation attenuation due to the changes in the chemical composition of the woods and the dependence of the attenuation coefficient on energy and densities of these woods. The descending order of attenuation coefficient determined are; Ayin, Oro, Anuje, Ako, Asunrun, Apa-igbo Gedu, Agbonyin, Opepe Oganwo, Iroko Odogi , Ayo, Ayunre, Afara, Omo, Melania, Akomu, Arere, Pine, Araba. For a constant energy of 0.101MeV, the attenuation coefficient are 0.190cm -1 , 0.165cm -1 , 0.163cm -1 , 0.156cm -1 , 0.149cm -1 , 0.143cm -1 , 0.133cm -1 , 0.132cm -1 , 0.127cm -1 , 0.124cm -1 , 0.085cm -1 , 0.123cm -1 , 0.122cm -1 , 0.113cm -1 , 0.101cm -1 , 0.088cm -1 , 0.087cm -1 , 0.086cm -1 , 0.082cm -1 respectively. The wood in descending order of dependence of attenuation coefficient on density are: Ayin,Oro, Anunje,Ako,Asunrun,Apa-Igbo, Gedu, Agbonyin, Opepe, Oganwo, Iroko, Odogi, Ijebo, Ayo, Ayunre, Afara, Omo, Melania, Akomu, Arere, Pine and Araba. The half value layer shows the thickness at various energy regions.

  3. 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...

  4. 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, ...

  5. 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...

  6. Spectrometric techniques 3

    CERN Document Server

    Vanasse, George A

    2013-01-01

    Spectrometric Techniques, Volume III presents the applications of spectrometric techniques to atmospheric and space studies. This book reviews the spectral data processing and analysis techniques that are of broad applicability.Organized into five chapters, this volume begins with an overview of the instrumentation used for obtaining field data. This text then reviews the contribution that space-borne spectroscopy in the thermal IR has made to the understanding of the planets. Other chapters consider the instruments that have recorded the planetary emission spectra. This book discusses as well

  7. Screening Natural Content of Water-Soluble B Vitamins in Fish: Enzymatic Extraction, HILIC Separation, and Tandem Mass Spectrometric Determination.

    Science.gov (United States)

    Chatterjee, Niladri Sekhar; Kumar, K Ashok; Ajeeshkumar, K K; Kumari, K R Remya; Vishnu, K V; Anandan, Rangasamy; Mathew, Suseela; Ravishankar, C N

    2017-05-01

    Despite the potential of LC with tandem MS (MS/MS) in improving sensitivity and selectivity, analytical methods are scarce for the determination of protein-bound and phosphorylated forms of B vitamins in food. This prompted us to develop a method for LC-MS/MS determination of naturally occurring nicotinamide, nicotinic acid, thiamine, pyridoxine, riboflavin, pantothenic acid, biotin, folic acid, and cyanocobalamin in fish. Baseline separation of the vitamins was achieved in a hydrophilic interaction LC condition. An ultrasonication-assisted enzymatic extraction protocol for sample preparation was optimized and validated. The time required for extraction was significantly reduced (to 4 h), while maintaining good extraction efficiency. Acetonitrile content (80%, v/v) in the prepared sample was found to be optimum for excellent peak shape and sensitivity. The dynamic linear range of the vitamins ranged from 2.5 to 500 ng/g, and the regression coefficient values were greater than 0.99. LOQ values ranged from 0.4 to 50 ng/g for the different vitamins. The spike recovery values at 50 and 100 ng/g ranged from 87.5 to 97.5%. The intra- and interday precision values were satisfactory. Accuracy of the developed method was determined by analysis of a Certified Reference Material. The method could also be used for unambiguous determination of the natural content of the target vitamins in fish.

  8. Improved analytical procedure for the determination of 210Pb and 210Po using alpha-spectrometric isotope dilution

    International Nuclear Information System (INIS)

    Urnezis, P.W.; Holtzman, R.B.

    1981-01-01

    An isotope dilution method has been incorporated into the 210 Pb- 210 Po analysis. A known amount of 209 Po is added to the sample before analysis. Then both 209 Po and 210 Po are deposited on a silver planchet which is assayed in an alpha spectrometer to determine the activities of each isotope. The recoveries generally range from 70% to 90%

  9. Determination of Pu-238 Abundance in a Plutonium Standard by an Advanced Thermal Ionization Mass Spectrometric Technique

    Science.gov (United States)

    Mason, P.; Thomas, R.

    2006-12-01

    New developments in thermal ionization mass spectrometers allow for the determination of very small minor isotope ratios. The new hardware and software capabilities require attention to detail and accounting for additional sources of measurement uncertainty. The Pu-238 isotopic composition in New Brunswick Laboratory plutonium metal standard CRM 126-A was determined by thermal ionization mass spectrometry using combined Faraday cup and ion counting detection. A dynamic acquisition scheme was employed which provided for near real-time mass fractionation correction and ion counter/Faraday detector inter-calibration. Steps taken to minimize or eliminate isobaric U-238 interferences will be described, and an evaluation detailing contributions to the uncertainty, including SEM non-linearity, will be presented.

  10. Energy dispersive x-ray fluorescence spectrometric determination of phosphorus, calcium, iron, zinc, and strontium in human bones

    International Nuclear Information System (INIS)

    Ohta, Akishige; Matsubayashi, Takashi; Itoman, Moritoshi

    1981-01-01

    Phosphorus, calcium, iron, zinc and strontium in a human bone extracted by surgery were determined by energy dispersive X-ray fluorescence spectrometry. The bone was decomposed with nitric acid, then diluted with water. A specific quantity of the solution was naturally dried on polyethylene film, and subjected to X-ray analysis. For determining the calibration curves in a mixture of phosphorus, calcium, iron, zinc and strontium, for the analysis of phosphorus and calcium, germanium was used as the secondary target and aluminum as the filter; and for the analysis of iron, zinc and strontium, molybdenum and molybdenum-aluminum were used, respectively. Consequently, the calibration curves were able to be obtained with high precision in the ranges from 5 to 500 μg of phosphorus, from 1 to 50 μg of calcium and from 0.1 to 1.0 μg of iron, zinc and strontium. In this way, in 1 mg of the human bone by wet weight, phosphorus, calcium, iron, zinc and strontium were able to be determined. (J.P.N.)

  11. GammaWorkshops Proceedings

    International Nuclear Information System (INIS)

    Ramebaeck, H.; Straelberg, E.; Klemola, S.; Nielsen, Sven P.; Palsson, S.E.

    2012-01-01

    Due to a sparse interaction during the last years between practioners in gamma ray spectrometry in the Nordic countries, a NKS activity was started in 2009. This GammaSem was focused on seminars relevant to gamma spectrometry. A follow up seminar was held in 2010. As an outcome of these activities it was suggested that the 2011 meeting should be focused on practical issues, e.g. different corrections needed in gamma spectrometric measurements. This three day's meeting, GammaWorkshops, was held in September at Risoe-DTU. Experts on different topics relevant for gamma spectrometric measurements were invited to the GammaWorkshops. The topics included efficiency transfer, true coincidence summing corrections, self-attenuation corrections, measurement of natural radionuclides (natural decay series), combined measurement uncertainty calculations, and detection limits. These topics covered both lectures and practical sessions. The practical sessions included demonstrations of tools for e.g. corrections and calculations of the above meantioned topics. (Author)

  12. Determination of burnup grade of fuel plates by gamma spectrometry

    International Nuclear Information System (INIS)

    Terremoto, Luis A.A.; Zeituni, Carlos A.; Perrotta, Jose A.

    1999-01-01

    This work describes absolute burnup measurements on spent MTR fuel elements by means of non-destructive gamma-ray spectroscopy which correlates activities of radioactive fission products with the fissioned mass of 235 U. Experiments based on such method were performed at the storage pool area of the IEA-R1 research reactor. The obtained results were compared with calculational ones based on neutronics. (author)

  13. Gas chromatographic-mass spectrometric determination of aromatic hydrocarbon metabolites from livers of fish exposed to fuel oil.

    Science.gov (United States)

    Krahn, M M; Malins, D C

    1982-10-15

    Metabolites of several two- and three-ring aromatic hydrocarbons (AHs) have been found in livers of English sole exposed to No. 2 fuel oil. Four metabolites of the C2H5-naphthalenes, six of the C3H7-naphthalenes and one each of fluorene, phenanthrene and anthracene have been partially characterized and their concentrations, which ranged from 50 to 1100 ng/g, were determined. Metabolites were separated from the liver matrix using an automated extractor/concentrator. The resulting extract was then purified by high-performance liquid chromatography, and the metabolites were characterized and quantitated by gas chromatography-mass spectrometry.

  14. Simultaneous determination of major type A and B trichothecenes, zearalenone and certain modified metabolites in Finnish cereal grains with a novel liquid chromatography-tandem mass spectrometric method.

    Science.gov (United States)

    Nathanail, Alexis V; Syvähuoko, Jenna; Malachová, Alexandra; Jestoi, Marika; Varga, Elisabeth; Michlmayr, Herbert; Adam, Gerhard; Sieviläinen, Elina; Berthiller, Franz; Peltonen, Kimmo

    2015-06-01

    A reliable and sensitive liquid chromatography-tandem mass spectrometric method was developed for the simultaneous quantitative determination in cereals of the Fusarium mycotoxins HT-2 toxin, T-2 toxin, deoxynivalenol, nivalenol and zearalenone, as well as the modified metabolites 3-acetyl-deoxynivalenol, α-zearalenol, β-zearalenol, deoxynivalenol-3-glucoside, HT-2-3-glucoside, nivalenol-3-glucoside, zearalenone-14-glucoside, zearalenone-14-sulphate, zearalenone-16-glucoside, α-zearalenol-14-glucoside and β-zearalenol-14-glucoside. The 'dilute and shoot' approach was used for sample preparation after extraction with acetonitrile:water:acetic acid (79:20:1, v/v/v). Separation was carried out using reversed-phase liquid chromatography, and detection was performed using tandem mass spectrometry in the selected reaction monitoring mode. The method was in-house validated according to performance characteristics, established in Commission Regulation EC No 401/2006 and Commission Decision EC No 657/2002, prior to its application in a nationwide survey for the analysis of barley, oat and wheat samples (n = 95) harvested in Finland during 2013. Deoxynivalenol and its glucosylated form were the most abundant of the analytes, being detected in 93 and 81 % of the samples, respectively. Concentrations of deoxynivalenol were unusually high in 2013, especially in oats, with some cases exceeding the maximum legislative limits for unprocessed oats placed on the market for first-stage processing. All modified mycotoxins analysed were detected, and the natural occurrence of some of these compounds (e.g. zearalenone-16-glucoside and nivalenol-3-glucoside) in barley, oats and/or wheat was documented for the first time.

  15. A liquid chromatography-tandem mass spectrometric method for quantitative determination of native 5-methyltetrahydrofolate and its polyglutamyl derivatives in raw vegetables.

    Science.gov (United States)

    Wang, Chao; Riedl, Ken M; Schwartz, Steven J

    2010-11-01

    Folate deficiency is a prevalent phenomenon worldwide especially in underprivileged countries. Polyglutamyl 5-methyltetrahydrofolate (5MTHF) species are the naturally occurring principle folate in store-bought vegetables. Here we report a simple and complete extraction method for the determination of native polyglutamyl 5-methyltetrahydrofolate in vegetables using high performance liquid chromatography with tandem mass spectrometric detection (HPLC-MS/MS). Coarsely chopped samples (18 different vegetables) were steamed to inactivate glutamylase enzymes and liberate folate from binding proteins and extracted in a reducing buffer with (13)C(5) 5MTHF stable isotope added as internal standard. The polyglutamyl 5-methyltetrahydrofolate species were separated in 9 min on a C(18) column using a reversed phase system. HPLC eluate was interfaced with a triple quadrupole mass spectrometer operated in electrospray positive mode. The respective pseudomolecular cation of each polyglutamyl 5-methyltetrahydrofolate species was selected for fragmentation to a common daughter ion for detection. We quantitated polyglutamyl 5-methyltetrahydrofolate in store-bought vegetables from families Brassicaceae, Asteraceae and Amaranthaceae (including mustard greens, romaine lettuce and Swiss chard) of which most have not been quantitated previously. Most vegetables from Asteraceae and those from Amaranthaceae contained similar amounts of monoglutamyl 5MTHF and polyglutamyl 5MTHF while Brassicaceae were dominated by polyglutamyls and endive species (Asteraceae) contained mainly monoglutamyl 5MTHF. The precision of the method for the various polyglutamyl 5-methyltetrahydrofolate forms was 1-9% RSD, recovery 84-91%, limit of detection 64-658 fmol and limit of quantitation 193-1994 fmol. Herein we describe a rapid, sensitive and selective HPLC-MS/MS technique to quantitate polyglutamyl 5-methyltetrahydrofolate species. This method may be suitable for analyzing the polyglutamyl 5

  16. A liquid chromatography–tandem mass spectrometric method for quantitative determination of native 5-methyltetrahydrofolate and its polyglutamyl derivatives in raw vegetables

    Science.gov (United States)

    Wang, Chao; Riedl, Ken M.; Schwartz, Steven J.

    2013-01-01

    Folate deficiency is a prevalent phenomenon worldwide especially in underprivileged countries. Polyglutamyl 5-methyltetrahydrofolate (5MTHF) species are the naturally occurring principle folate in store-bought vegetables. Here we report a simple and complete extraction method for the determination of native polyglutamyl 5-methyltetrahydrofolate in vegetables using high performance liquid chromatography with tandem mass spectrometric detection (HPLC–MS/MS). Coarsely chopped samples (18 different vegetables) were steamed to inactivate glutamylase enzymes and liberate folate from binding proteins and extracted in a reducing buffer with 13C5 5MTHF stable isotope added as internal standard. The polyglutamyl 5-methyltetrahydrofolate species were separated in 9 min on a C18 column using a reversed phase system. HPLC eluate was interfaced with a triple quadrupole mass spectrometer operated in electrospray positive mode. The respective pseudomolecular cation of each polyglutamyl 5-methyltetrahydrofolate species was selected for fragmentation to a common daughter ion for detection. We quantitated polyglutamyl 5-methyltetrahydrofolate in store-bought vegetables from families Brassicaceae, Asteraceae and Amaranthaceae (including mustard greens, romaine lettuce and Swiss chard) of which most have not been quantitated previously. Most vegetables from Asteraceae and those from Amaranthaceae contained similar amounts of monoglutamyl 5MTHF and polyglutamyl 5MTHF while Brassicaceae were dominated by polyglutamyls and endive species (Asteraceae) contained mainly monoglutamyl 5MTHF. The precision of the method for the various polyglutamyl 5-methyltetrahydrofolate forms was 1–9% RSD, recovery 84–91%, limit of detection 64–658 fmol and limit of quantitation 193–1994 fmol. Herein we describe a rapid, sensitive and selective HPLC–MS/MS technique to quantitate polyglutamyl 5-methyltetrahydrofolate species. This method may be suitable for analyzing the polyglutamyl 5

  17. A novel, donor-active solvent-assisted liquid-phase microextraction procedure for spectrometric determination of zinc

    Energy Technology Data Exchange (ETDEWEB)

    Kocurova, Livia; Fatlova, Martina; Bazel, Yaroslav; Serbin, Rastislav; Andruch, Vasil, E-mail: liviamonika.kocurova@gmail.com [Department of Analytical Chemistry, University of P. J. Safarik, Kosice (Slovakia); Balogh, Ioseph S. [Department of Chemistry, College of Nyiregyhaza (Hungary); Simon, Andras [Department of General and Analytical Chemistry, Budapest University of Technology and Economics, Budapest (Hungary); Badida, Miroslav; Rusnak, Radoslav [Department of Environmentalistics, Faculty of Mechanical Engineering, Technical University of Kosice (Slovakia)

    2014-02-15

    Based on the reaction of Zn(II), thiocyanate and 2-[2-(5-dimethylamino-thiophen-2-yl)-vinyl]- 1,3,3-trimethyl-3H-indolium bromide (DTVTI), a donor-active solvent-assisted liquid-phase microextraction procedure followed by spectrophotometric determination of zinc at 570 nm was developed. The optimum experimental conditions were investigated and found to be as follows: concentration of NH{sub 4}SCN 0.02 mol L{sup -1} concentration of DTVTI 4 x 10{sup -5} mol L{sup -1}. Various extraction solvents were studied alone as well as in mixtures with different improvers, and a mixture of toluene as the extraction solvent and tributylphosphate as the donor-active solvent in a 4:1 v/v ratio was selected. The calibration plot was linear up to 2.62 mg L{sup 1} of zinc with limit of detection 0.09 mg L{sup -1}. The developed procedure was applied for zinc determination in dietary supplements. (author)

  18. Standard test method for graphite furnace atomic absorption spectrometric determination of lead and cadmium extracted from ceramic foodware

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2000-01-01

    1.1 This test method covers procedures for using graphite furnace atomic absorption spectroscopy (GFAAS) to quantitatively determine lead and cadmium extracted by acetic acid at room temperature from the food-contact surface of foodware. The method is applicable to food-contact surfaces composed of silicate-based materials (earthenware, glazed ceramicware, decorated ceramicware, decorated glass, and lead crystal glass) and is capable of determining lead concentrations greater than 0.005 to 0.020 g/mL and cadmium concentrations greater than 0.0005 to 0.002 g/mL, depending on instrument design. 1.2 This test method also describes quality control procedures to check for contamination and matrix interference during GFAAS analyses and a specific sequence of analytical measurements that demonstrates proper instrument operation during the time period in which sample solutions are analyzed. 1.3 Cleaning and other contamination control procedures are described in this test method. Users may modify contamination cont...

  19. Study on direct determination of uranium and efficient equilibrium factor by gamma-ray spectrometer

    International Nuclear Information System (INIS)

    Liu Chunkui

    1990-01-01

    The test principle, test set and surveying methods for conducting gamma-ray spectrometry on conveyer are presented. The conversion coefficient of the spectrometer has been found by using duallinear regression analysis of uranium and radon and their higher and lower bands of gamma-ray spectra. The efficient equilibrium factor can be quickly determined, and the direct determination of uranium in the non-equilibrium condition of uranium and radium can be made

  20. Separation and enrichment of gold(III) from environmental samples prior to its flame atomic absorption spectrometric determination

    International Nuclear Information System (INIS)

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

    2007-01-01

    A simple and accurate method was developed for separation and enrichment of trace levels of gold in environmental samples. The method is based on the adsorption of Au(III)-diethyldithiocarbamate complex on Amberlite XAD-2000 resin prior to the analysis of gold by flame atomic absorption spectrometry after elution with 1 mol L -1 HNO 3 in acetone. Some parameters including nitric acid concentration, eluent type, matrix ions, sample volume, sample flow rate and adsorption capacity were investigated on the recovery of gold(III). The recovery values for gold(III) and detection limit of gold were greater than 95% and 16.6 μg L -1 , respectively. The preconcentration factor was 200. The relative standard deviation of the method was -1 . The validation of the presented procedure was checked by the analysis of CRM-SA-C Sandy Soil certified reference material. The presented procedure was applied to the determination of gold in some environmental samples

  1. Development of a portable mass spectrometric system for determination of isotopic composition of solid uranium samples using fluorine volatilization

    Science.gov (United States)

    Loge, G.

    1994-09-01

    Using hardware and materials supplied by LANL, a prototype quadrupole mass spectrometer system designed for portable field analysis of isotopic composition of solid uranium samples was assembled and tested. The system contained the capability for fluorine volatilization of solid uranium samples with gas introduction, which was successfully tested and demonstrated using 100 mg samples of U3O8. Determination of precision and accuracy for measuring isotopic composition was performed using isotopic standards. Use with soil samples containing uranium were also attempted. Silicates in the soil forming SiF4 were found to be a kinetic bottleneck to the formation of UF6. This could be avoided by performing some sort of chemical separation as a pre-treatment step, which was demonstrated using nitric acid.

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

    International Nuclear Information System (INIS)

    Prohaska, C.

    2002-05-01

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

  3. Selective cloud point extraction and graphite furnace atomic absorption spectrometric determination of molybdenum (VI) ion in seawater samples

    Energy Technology Data Exchange (ETDEWEB)

    Filik, Hayati, E-mail: filik@istanbul.edu.tr [Istanbul University, Faculty of Engineering, Department of Chemistry, Avcilar, 34320 Istanbul (Turkey); Cengel, Tayfun; Apak, Resat [Istanbul University, Faculty of Engineering, Department of Chemistry, Avcilar, 34320 Istanbul (Turkey)

    2009-09-30

    A cloud point extraction process using the nonionic surfactant Triton X-114 to extract molybdenum from aqueous solutions was investigated. The method is based on the complexation reaction of Mo(VI) with 1,2,5,8-tetrahydroxyanthracene-9,10-dione (quinalizarine: QA) and micelle-mediated extraction of the complex. The enriched analyte in the surfactant-rich phase was determined by graphite furnace atomic absorption spectrometry (GFAAS). The optimal extraction and reaction conditions (e.g. pH, reagent and surfactant concentrations, temperature, incubation and centrifugation times) were evaluated and optimized. Under the optimized experimental conditions, the limit of detection (LOD) for Mo(VI) was 7.0 ng L{sup -1} with an preconcentration factor of {approx}25 when 10 mL of sample solution was preconcentrated to 0.4 mL. The proposed method (with extraction) showed linear calibration within the range 0.03-0.6 {mu}g L{sup -1}. The relative standard deviation (RSD) was found to be 3.7% (C{sub Mo(VI)} = 0.05 {mu}g L{sup -1}, n = 5) for pure standard solutions, whereas RSD for the recoveries from real samples ranged between 2 and 8% (mean RSD = 3.9%). The method was applied to the determination of Mo(VI) in seawater and tap water samples with a recovery for the spiked samples in the range of 98-103%. The interference effect of some cations and anions was also studied. In the presence of foreign ions, no significant interference was observed. In order to verify the accuracy of the method, a certified reference water sample was analysed and the results obtained were in good agreement with the certified values.

  4. Aerial gamma spectrometric survey as a tool for evaluating the uranium remobilization degree: Case study from Al-Awabed area, Northern Palmyrides, Syria

    International Nuclear Information System (INIS)

    Asfahani, J.; Al-Hent, R.; Aissa, M.

    2009-01-01

    The relationships between equivalent uranium (eU), eTh, K% and their ratios in the 11 lithological units determined by previous research in the Al-Awabed area, Northern Palmyrides, Syria have been analyzed in order to define their trend variations and evaluate the degree of uranium remobilization. Uranium favorability index U I and alteration-F indicators have been used in this research to characterize the different lithological units by following their radioactive element re-distribution and to determine their favorability as regards uranium potentiality. It was shown that uranium remobilization took place in all the lithological units, but to different degrees. This remobilization is qualified as weak, indicating that limited uranium redistribution is expected in the studied region. A plausible geological model is proposed for the uranium distribution, where the Abou Qila location is found to be favorable for uranium accumulation and merits further uranium exploration. (Authors)

  5. Determination of nine high-intensity sweeteners in various foods by high-performance liquid chromatography with mass spectrometric detection.

    Science.gov (United States)

    Zygler, Agata; Wasik, Andrzej; Kot-Wasik, Agata; Namieśnik, Jacek

    2011-06-01

    An analytical procedure involving solid-phase extraction (SPE) and high-performance liquid chromatography-mass spectrometry has been developed for the determination of nine high-intensity sweeteners authorised in the EU; acesulfame-K (ACS-K), aspartame (ASP), alitame (ALI), cyclamate (CYC), dulcin (DUL), neohesperidin dihydrochalcone (NHDC), neotame (NEO), saccharin (SAC) and sucralose (SCL) in a variety of food samples (i.e. beverages, dairy and fish products). After extraction with a buffer composed of formic acid and N,N-diisopropylethylamine at pH 4.5 in ultrasonic bath, extracts were cleaned up using Strata-X 33 μm Polymeric SPE column. The analytes were separated in gradient elution mode on C(18) column and detected by mass spectrometer working with an electrospray source in negative ion mode. To confirm that analytical method is suitable for its intended use, several validation parameters, such as linearity, limits of detection and quantification, trueness and repeatibilty were evaluated. Calibration curves were linear within a studied range of concentrations (r(2) ≥ 0.999) for six investigated sweeteners (CYC, ASP, ALI, DUL, NHDC, NEO). Three compounds (ACS-K, SAC, SCL) gave non-linear response in the investigated concentration range. The method detection limits (corresponding to signal-to-noise (S/N) ratio of 3) were below 0.25 μg mL(-1) (μg g(-1)), whereas the method quantitation limits (corresponding to S/N ratio of 10) were below 2.5 μg mL(-1) (μg g(-1)). The recoveries at the tested concentrations (50%, 100% and 125% of maximum usable dose) for all sweeteners were in the range of 84.2 ÷ 106.7%, with relative standard deviations beverage, yoghurt, fish product) and the spiking level. The proposed method has been successfully applied to the determination of the nine sweeteners in drinks, yoghurts and fish products. The procedure described here is simple, accurate and precise and is suitable for routine quality control analysis of

  6. Ultra-performance liquid chromatography-tandem mass spectrometric method for the determination of strychnine and brucine in mice plasma.

    Science.gov (United States)

    Liu, Yanwen; Zhu, Ronghua; Li, Huande; Yan, Miao; Lei, Yanqing

    2011-09-15

    A selective, simple and efficient method-ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was developed for determination of two toxic alkaloids, namely strychnine and brucine in mice plasma. The UPLC separation was carried out using a 1.7 μm BEH C(18) column (50 mm × 2.1 mm) with a mobile phase consisting of methanol:0.1% formic acid (25:75, v/v), hence providing high efficiency, high resolution and excellent peak shape for the analytes and internal standard. The method was validated over the range of 2.48-496.4 ng/ml for strychnine and 2.64-528 ng/ml for brucine, respectively. Intra- and inter-day accuracy ranged from 95.0% to 107.9% for strychnine, 93.4% to 103.3% for brucine, and the precisions were within 13.8%. The extraction recoveries of both the two alkaloids exceed 81.9%. With a simple and minor sample preparation procedure and short run-time (strychnine and brucine in vivo. Copyright © 2011 Elsevier B.V. All rights reserved.

  7. Separation and enrichment of gold(III) from environmental samples prior to its flame atomic absorption spectrometric determination

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-10-22

    A simple and accurate method was developed for separation and enrichment of trace levels of gold in environmental samples. The method is based on the adsorption of Au(III)-diethyldithiocarbamate complex on Amberlite XAD-2000 resin prior to the analysis of gold by flame atomic absorption spectrometry after elution with 1 mol L{sup -1} HNO{sub 3} in acetone. Some parameters including nitric acid concentration, eluent type, matrix ions, sample volume, sample flow rate and adsorption capacity were investigated on the recovery of gold(III). The recovery values for gold(III) and detection limit of gold were greater than 95% and 16.6 {mu}g L{sup -1}, respectively. The preconcentration factor was 200. The relative standard deviation of the method was <6%. The adsorption capacity of the resin was 12.3 mg g{sup -1}. The validation of the presented procedure was checked by the analysis of CRM-SA-C Sandy Soil certified reference material. The presented procedure was applied to the determination of gold in some environmental samples.

  8. Mass spectrometric determination of enthalpies of dissociation of gaseous complex fluorides into neutral and charged particles. Pt. 3

    International Nuclear Information System (INIS)

    Sidorov, L.N.; Skokan, E.V.; Nikitin, M.I.; Sorokin, I.D.

    1980-01-01

    Mass spectrometry is used to study ion-molecule equilibria in the saturated vapours of the two-component systems MF-UF 4 (where M is Na or K), containing the negative ions F - , UF - 5 and UF - 6 . The electron affinities of UF 5 and UF 6 are determined as 3.3 +- 0.16 eV and 4.89 +- 0.25 eV and the heats of the following reactions are: F - + UF 4 → UF - 5 ΔH 0 1100 = -98,0 +- 0.3 kcal mol -1 (-410.0 +- 1.3 kJ mol -1 ), AlF 3 + UF - 5 → AlF - 4 + UF 4 ΔH 0 1100 = -22.3 +- 0.3 kcal mol -1 (-93.3 +- 1.3 kJ mol -1 ), UF 5 + UF - 5 → UF 4 + UF - 6 ΔH 0 1087 = -3.4 +- 0.2 kcal mol -1 (-14.2 +- 0.8 kJ mol -1 ). These data and literature values are used to calculate the heat of formation of the UF - 5 ion and the heats of dissociation of the alkali metal fluorouranates into neutral and charged particles. (orig.)

  9. A simple method for the absolute determination of uranium enrichment by high-resolution {gamma} spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Korob, R.O. [Unidad de Actividad Radioquimica y Quimica de las Radiaciones, Comision Nacional de Energia Atomica, Centro Atomico Ezeiza, Presbitero Juan Gonzalez y Aragon No. 15 Partido de Ezeiza, Provincia de Buenos Aires (Argentina)]. E-mail: korob@cae.cnea.gov.ar; Blasiyh Nuno, G.A. [Unidad de Actividad Gestion de Residuos Radiactivos, Comision Nacional de Energia Atomica, Centro Atomico Ezeiza, Presbitero Juan Gonzalez y Aragon No. 15 Partido de Ezeiza, Provincia de Buenos Aires (Argentina)

    2006-05-15

    A simple method for the determination of uranium enrichment using high-resolution {gamma} spectrometry is presented in this paper. The method relies solely on the {gamma}-ray emission probabilities of {sup 235}U and {sup 234m}Pa, and an iterative procedure for the least squares fit of a polynomial to a set of experimentally determined data. To ensure the reliability of the {sup 234m}Pa {gamma}-ray emission probabilities employed, a new determination of these probabilities was carried out using a combination of {gamma} spectrometry and Cerenkov counting of a purified {sup 234}Th solution. Using these new data, a maximum difference of {approx}5% has been found between the experimental and declared uranium enrichment in a set of solid and liquid samples containing uranium compounds.

  10. Realisation of a {beta} spectrometer solenoidal and a double {beta} spectrometer at coincidence; Realisation d'un spectrometre {beta} solenoidal et d'un double spectrometre {beta} a coincidence

    Energy Technology Data Exchange (ETDEWEB)

    Moreau, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1955-06-15

    The two spectrometers have been achieved to tackle numerous problems of nuclear spectrometry. They possess different fields of application that complete themselves. The solenoidal spectrometer permits the determination of the energy limits of {beta} spectra and of their shape; it also permits the determination of the coefficients of internal conversion and reports {alpha}{sub K} / {alpha}{sub L} and it is especially efficient for the accurate energy levels of the {gamma} rays by photoelectric effect. The double coincidence spectrometer has been conceived to get a good efficiency in coincidence: indeed, the sum of the solid angles used for the {beta} and {gamma} emission is rather little lower to 4{pi} steradians. To get this efficiency, one should have sacrificed a little the resolution that is lower to the one obtained with the solenoidal spectrometer for a same brightness. Each of the elements of the double spectrometer can also be adapted to the study of angular correlations {beta}{gamma} and e{sup -}{gamma}. In this use, it is superior to the thin magnetic lens used up to here. The double spectrometer also permits the survey of the coincidences e{sup -}e{sup -}, e{sup -}{beta} of a equivalent way to a double lens; it can also be consider some adaptation for the survey of the angular correlations e{sup -}e{sup -}, e{sup -}{beta}. Finally, we applied the methods by simple spectrometry and by coincidence spectrometry, to the study of the radiances of the following radioelements: {sup 76}As (26 h), {sup 122}Sb (2,8 j), {sup 124}Sb (60 j), {sup 125}Sb (2,7 years). (M.B.) [French] Les deux spectrometres qui ont ete realises permettent d'aborder un grand nombre de problemes de spectrometrie nucleaire. Ils possedent des champs d'application tres differents qui se completent. Le spectrometre solenoidal permet la determination des energies limites des spectres {beta} et de leur forme; il permet aussi la determination des coefficients de conversion interne et

  11. Liquid chromatographic-mass spectrometric method for ...

    African Journals Online (AJOL)

    spectrometric (LC-MS/MS) method for the quantitative determination of two dermatological drugs,. Lamisil® (terbinafine) and Proscar® (finasteride), in split tablet dosage form. Methods: Thirty tablets each of the 2 studied medications were randomly selected. Tablets were weighed and divided into 3 groups. Ten tablets of ...

  12. In-situ gamma spectrometry method for determination of environmental gamma dose; Metodo de espectrometria gamma in situ para determinacao de dose gama ambiental

    Energy Technology Data Exchange (ETDEWEB)

    Conti, Claudio de Carvalho

    1995-07-15

    This work tries to establish a methodology for germanium detectors calibration, normally used for in situ gamma ray spectrometry, for determining the environmental exposure rate in function of the energy of the incident photons. For this purpose a computer code has been developed, based on the stripping method, for the computational spectra analysis to calculate the contribution of the partial absorption of the gamma rays (Compton effect) in the active and nonactive parts of the detector. The resulting total absorption spectrum is then converted to fluence distribution in function of the energy for the photons reaching the detector, which is then used to calculate the exposure rate or kerma in air. The unfolding and fluency convention parameters are determined by detector calibration using point gamma sources. The method is validated by comparison of the results against the calculated exposure rate at a point of interest for the standards. This method is used for the direct measurement of the exposure rate distribution in function of the energy at the site, in situ measurement technic, leading to rapid results during an emergency situation and also used for indoor measurements. (author)

  13. A finite element based algorithm for determining interfacial tension (gamma) from pendant drop profiles.

    Science.gov (United States)

    Dingle, Nicole M; Tjiptowidjojo, Kristianto; Basaran, Osman A; Harris, Michael T

    2005-06-15

    This paper introduces a robust algorithm to determine the interfacial tension (gamma) from pendant drop profiles using the Galerkin finite element method (gamma-PD-FEM) to solve the axisymmetric form of the Young-Laplace (YL) equation. In this algorithm, the theoretical profiles are generated by solving the spherical coordinate form of the YL equation. gamma-PD-FEM also solves for the parameter estimates by minimizing the difference between the theoretical and experimental surface functions, f(theta). This technique is compared to the widely used method of converting the YL equation to the three arc length-based (ALB) first-order ODEs developed by Bashforth and Adams (BA) in 1883, or as denoted in this paper, the gamma-PD-BA method. The drop apex is the initial condition for the gamma-PD-BA algorithm and the integration is terminated at a specified location along the drop profile. In contrast to techniques based on the BA approach, computation of the theoretical drop profile in gamma-PD-FEM is obtained from a second-order ordinary differential equation and requires boundary conditions at the drop apex and at the contact line of the drop to the nozzle. By incorporating both boundary conditions into the problem formulation, the algorithm can also determine if the drop shape is at static equilibrium. Results to be presented include an outline of the computer algorithm, and comparison of gamma values obtained from the gamma-PD-FEM and the traditional gamma-PD-BA method using simulated and experimental drop profile data sets.

  14. Determination of Natural Radioactivity in Building Materials with Gamma Spectrometry

    International Nuclear Information System (INIS)

    Turki, Faten

    2010-01-01

    In the setting of this work, the natural radioactivity of building materials used in Tunisia has been measured by gamma spectrometry. These products have been ground and dried at 100 degree for 12 h. Then, they have been homogenized, weighed and finally conditioned during 23 days in order to reach the radioactive equilibrium. The measures' results proved that all building materials studied except bauxite and the ESC clay, possess doses lower than the acceptable limit (1 mSv.an-1). However, the possibility of reinforcement of the natural radioactivity in some industry of building can exist. To insure that the cement, the most used in the world, don't present any radiological risk on the workers' health, a survey has been made in the factory - les Ciments de Bizerte - about its manufacture's process. The results of this survey showed that this product can be considered like a healthy product.

  15. Holmium-166m: multi-gamma standard to determine the activity of radionuclides in semiconductor detectors

    International Nuclear Information System (INIS)

    Bernardes, Estela Maria de Oliveira

    2001-01-01

    The efficiency and calibration curves as function of gamma-ray energy for a germanium detector are usually established by using many standard gamma ray sources of radionuclides decaying with few gamma rays or radionuclides having complex decay scheme, as 152 Eu or 133 Ba. But these radionuclides cannot be used alone, because they have a few gamma lines with high intensity and these lines have a irregular distribution in the energy spectrum. 166m Ho is found to be a convenient single source for such calibration, because it decays by β - with subsequent emission of about 40 strong and well distributed gamma lines between 80 and 1500 keV. Moreover, its long half - life (1200 years) and X-rays characteristics between 40 and 50 keV makes it a good standard for calibration of germanium detectors. However, it is necessary to know with accuracy and precision the gamma ray intensities of their main lines, due to the fact that literature has showed discrepant values. Then, a methodology to determine the emission probability of its main lines is proposed by means of combined use of gamma spectrometry and coincidence 4πβ -γ techniques. The experimental results show consistence to the others authors, with lower or compatible uncertainties. (author)

  16. Liquid chromatographic mass spectrometric (LC/MS/MS) determination of plasma hydroxocobalamin and cyanocobalamin concentrations after hydroxocobalamin antidote treatment for cyanide poisoning.

    Science.gov (United States)

    Schwertner, Harvey A; Valtier, Sandra; Bebarta, Vikhyat S

    2012-09-15

    Cyanide poisoning occurs in individuals after fire smoke inhalation and after oral ingestion of cyanide. Hydroxocobalamin (HOCbl), a hydroxylated form of vitamin B(12), is often used as an antidote to treat cyanide toxicity. It has a high affinity for cyanide and rapidly removes cyanide from tissue by forming cyanocobalamin (CNCbl). Little information is available on the pharmacokinetics of HOCbl and CNCbl largely because of the lack of analytical methods for analyzing HOCbl and CNCbl. In this study, we developed a new liquid chromatographic mass spectrometric (LC/MS/MS) method for the quantitative analysis of plasma HOCbl and CNCbl in the porcine (Sus scrofa) model. The method uses on-column extraction, reversed phase gradient chromatography, and multiple reaction monitoring (MRM) for quantitation. MRM transitions monitored were 664.7→147.3 and 664.7→359.2 for HOCbl and 678.8→147.3, 678.8→359.1 678.8→457.1 for CNCbl. The limit of detection (LOD) and the lower limit of quantitation (LLOQ) were 1.0 and 1.0 μmole/L, respectively, for plasma HOCbl and 0.1 and 0.5 μmole/L for plasma CNCbl. The within-day and between-day CVs were 4.3 and 6.4% for plasma HOCbl at 500.0 μmole/L and 5.5 and 5.7% for CNCbl at 100.0 μmole/L (n=6). The plasma HOCbl and CNCbl calibrations curves were linear from 100.0 to 2000.0 and 50.0 to 500.0 μmole/L, respectively. Based on 6 separate calibration curves the average linear regression coefficient (R(2)) for both HOCbl and CNCbl was 0.992. The LC/M/MS method was found to be accurate and precise and has been validated by determining the plasma HOCbl and CNCbl concentrations in 11 pigs that were treated with HOCbl for cyanide poisoning. Published by Elsevier B.V.

  17. Determining a pre-mining radiological baseline from historic airborne gamma surveys: A case study

    International Nuclear Information System (INIS)

    Bollhöfer, Andreas; Beraldo, Annamarie; Pfitzner, Kirrilly; Esparon, Andrew; Doering, Che

    2014-01-01

    Knowing the baseline level of radioactivity in areas naturally enriched in radionuclides is important in the uranium mining context to assess radiation doses to humans and the environment both during and after mining. This information is particularly useful in rehabilitation planning and developing closure criteria for uranium mines as only radiation doses additional to the natural background are usually considered ‘controllable’ for radiation protection purposes. In this case study we have tested whether the method of contemporary groundtruthing of a historic airborne gamma survey could be used to determine the pre-mining radiological conditions at the Ranger mine in northern Australia. The airborne gamma survey was flown in 1976 before mining started and groundtruthed using ground gamma dose rate measurements made between 2007 and 2009 at an undisturbed area naturally enriched in uranium (Anomaly 2) located nearby the Ranger mine. Measurements of 226 Ra soil activity concentration and 222 Rn exhalation flux density at Anomaly 2 were made concurrent with the ground gamma dose rate measurements. Algorithms were developed to upscale the ground gamma data to the same spatial resolution as the historic airborne gamma survey data using a geographic information system, allowing comparison of the datasets. Linear correlation models were developed to estimate the pre-mining gamma dose rates, 226 Ra soil activity concentrations, and 222 Rn exhalation flux densities at selected areas in the greater Ranger region. The modelled levels agreed with measurements made at the Ranger Orebodies 1 and 3 before mining started, and at environmental sites in the region. The conclusion is that our approach can be used to determine baseline radiation levels, and provide a benchmark for rehabilitation of uranium mines or industrial sites where historical airborne gamma survey data are available and an undisturbed radiological analogue exists to groundtruth the data. - Highlights:

  18. Determination of 210Pb in marine sediment core- A comparison between alpha and gamma techniques

    International Nuclear Information System (INIS)

    Zal Uyun Wan Mahmood; Yii Mei Wo; Zaharudin Ahmad

    2010-01-01

    The most commonly used techniques of alpha and gamma spectrometry were performed to measure 210 Pb activity in marine sediment core as a comparison. Alpha analytical technique measured the activity of 210 Pb from its in-grow grand-daughter 210 Po after a chemical separation, assuming radioactive equilibrium between the two radionuclides. Meanwhile, gamma analysis technique allows direct measurement, non-destructive and no preliminary chemical separation. Through the comparison, it is found that both alpha and gamma analysis techniques were slightly difference. Overall, the results from alpha analytical technique were basically higher than those from the gamma analytical techniques. Some logical argument had been discussed to explain this situation. In routine analysis, the analytical technique used should be chosen carefully based on advantages and disadvantages of the each technique and analysis requirements. Therefore, it is recommended to determine exactly the needs and purpose of analysis and to know the sample history before decide the appropriate analytical technique. (author)

  19. Primary radioactivity standardization and gamma intensities determination of {sup 124}Sb

    Energy Technology Data Exchange (ETDEWEB)

    Iwahara, A. [Laboratorio Nacional de Metrologia das Radiacoes Ionizantes (LNMRI)/Instituto de Radioprotecao e Dosimetria (IRD)/Comissao Nacional de Energia Nuclear - CNEN, Av. Salvador Allende, s/no, Recreio, CEP 22780-160, Rio de Janeiro (Brazil)], E-mail: iwahara@ird.gov.br; Delgado, J.U.; Poledna, R.; Silva, C.J. da; Almeida, M.C.M. de; Silva, R.L. da [Laboratorio Nacional de Metrologia das Radiacoes Ionizantes (LNMRI)/Instituto de Radioprotecao e Dosimetria (IRD)/Comissao Nacional de Energia Nuclear - CNEN, Av. Salvador Allende, s/no, Recreio, CEP 22780-160, Rio de Janeiro (Brazil)

    2009-04-21

    A solution containing {sup 124}Sb was primarily standardized by the 4{pi}{beta}-{gamma} coincidence and anticoincidence extrapolation methods in the frame of the EUROMET 907 international comparison organized by Laboratoire National Henri Bequerel (LNHB)/France, in 2007. The main purposes of this exercise are the improvement in the uncertainties on the gamma-ray emission intensities and they clarify the discrepancies verified among the intensity values for many weak gamma rays reported in the literature. In this work the results of the activity obtained were used to determine the absolute and relative gamma-ray intensities using a planar and coaxial HPGe detectors calibrated by {sup 152}Eu and {sup 116m}Ho multi-gamma standard sources covering the energy range from 20 to 1408 keV. Additionally the half-life of {sup 124}Sb was determined following the decay of a solution of {sup 124}Sb contained in a glass ampoule over a period of three half-lives using two 4{pi}{gamma} ionization chambers.

  20. Determining a pre-mining radiological baseline from historic airborne gamma surveys: a case study.

    Science.gov (United States)

    Bollhöfer, Andreas; Beraldo, Annamarie; Pfitzner, Kirrilly; Esparon, Andrew; Doering, Che

    2014-01-15

    Knowing the baseline level of radioactivity in areas naturally enriched in radionuclides is important in the uranium mining context to assess radiation doses to humans and the environment both during and after mining. This information is particularly useful in rehabilitation planning and developing closure criteria for uranium mines as only radiation doses additional to the natural background are usually considered 'controllable' for radiation protection purposes. In this case study we have tested whether the method of contemporary groundtruthing of a historic airborne gamma survey could be used to determine the pre-mining radiological conditions at the Ranger mine in northern Australia. The airborne gamma survey was flown in 1976 before mining started and groundtruthed using ground gamma dose rate measurements made between 2007 and 2009 at an undisturbed area naturally enriched in uranium (Anomaly 2) located nearby the Ranger mine. Measurements of (226)Ra soil activity concentration and (222)Rn exhalation flux density at Anomaly 2 were made concurrent with the ground gamma dose rate measurements. Algorithms were developed to upscale the ground gamma data to the same spatial resolution as the historic airborne gamma survey data using a geographic information system, allowing comparison of the datasets. Linear correlation models were developed to estimate the pre-mining gamma dose rates, (226)Ra soil activity concentrations, and (222)Rn exhalation flux densities at selected areas in the greater Ranger region. The modelled levels agreed with measurements made at the Ranger Orebodies 1 and 3 before mining started, and at environmental sites in the region. The conclusion is that our approach can be used to determine baseline radiation levels, and provide a benchmark for rehabilitation of uranium mines or industrial sites where historical airborne gamma survey data are available and an undisturbed radiological analogue exists to groundtruth the data. © 2013.

  1. Determination of spins and radioactive widths of tellurium nuclear levels with capturre gamma rays

    International Nuclear Information System (INIS)

    Bianchini, F.G.

    1973-01-01

    Spins and levels widths of the tellurium, mainly 128 Te and 130 Te, were determinated by gamma spectroscopy. Measurements of inelastic and elastic scattering, angular distribution and scattering temperature dependence, were still made. Energy levels of this isotopes, were also determinated [pt

  2. Determination of protein content in seeds by prompt gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Carbonari, A.W.; Pecequilo, B.R.S.

    1984-01-01

    The protein level in seeds can be directly calculated through the determination of the nitrogen content in grains. The authors show here that the radioactive thermal neutron capture prompt gamma-rays technique can be used to determine the nitrogen content in grains without chemical destruction, with good precision and relative rapidity, by detecting the prompt gamma rays emitted by the 14 N(n,γ) 15 N reaction product. The samples were irradiated in the tangential tube of the IEA-R1 research reactor, in Sao Paulo, and a pair spectrometer was used for the detection of the prompt gamma-rays. The nitrogen content was determined in several samples of soybean, common bean, peas and rice and the results compared with typical nitrogen content values for each grain. 33 references, 1 figure, 1 table

  3. 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)

  4. Study concerning the possibility of gamma-spectroscopy method to determining the total potassium in soils

    International Nuclear Information System (INIS)

    Leah, Tamara; Lozovaia, Zoia

    2011-01-01

    The paper presents the results of scientific research related to development the specifically express-method for determining total potassium in podsolic soils from Belarus and chernozem from Moldova, based on the use of gamma-spectrometry. Determining the precise of the total content of potassium in the soils can be made directly in the field or laboratory by gamma-spectroscopy method using radiation detection of natural isotope 40 K. The conversion coefficient for podsolic soils of Belarus is C=0,00395, for chernozem of Moldova - C=0,00337. (authors)

  5. Liquid chromatography/tandem mass spectrometric confirmatory method for determining aflatoxin M1 in cow milk: comparison between electrospray and atmospheric pressure photoionization sources.

    Science.gov (United States)

    Cavaliere, Chiara; Foglia, Patrizia; Pastorini, Elisabetta; Samperi, Roberto; Laganà, Aldo

    2006-01-06

    A liquid chromatography/electrospray (ESI)-tandem mass spectrometric method for the measurement of aflatoxin M1 (AFM1) in milk is described. Milk sample after protein precipitation with acetone was cleaned-up with a Carbograph-4 cartridge. Performances of the ESI source were compared with those of the atmospheric pressure photoionization source (APPI). Although a method quantification limit (MQL) of 6 ng/kg could be achieved operating with APPI source with respect to an MQL of 12 ng/kg with ESI, all the other performances being similar, then ESI was preferred as being more robust and widespread at present.

  6. A universal gamma-gamma method for simultaneous determination of rock and ore properties

    International Nuclear Information System (INIS)

    Charbucinski, J.

    1983-01-01

    A method for the simultaneous determination of heavy element content, density, borehole diameter and grain size is described, which is based on investigation of the changes in spectrum shape. By analysing these changes in a quantitative manner, information regarding the physical parameters of the medium can be obtained. The results of laboratory tests of the method are presented. (author)

  7. Borehole Logging for Uranium by Gamma-Ray Spectrometry

    DEFF Research Database (Denmark)

    Løvborg, Leif; Nyegaard, P.; Christiansen, E. M.

    1980-01-01

    The resources in a large syngenetic deposit of low-grade uranium (U) ore with thorium at Kvanefjeld, South Greenland, were evaluated by spectrometric gamma-ray logging of 23 boreholes, 46 mm in diameter and 200 m deep. The borehole probe's detector contained 22 cm3 of sodium-iodide, and the photo......The resources in a large syngenetic deposit of low-grade uranium (U) ore with thorium at Kvanefjeld, South Greenland, were evaluated by spectrometric gamma-ray logging of 23 boreholes, 46 mm in diameter and 200 m deep. The borehole probe's detector contained 22 cm3 of sodium...... of the spectrometer system were determined by calculating the average number of U and thorium (Th) counts per meter of borehole and comparing these with the U-Th concentrations in 1-m sections of analyzed drill core. The sensitivity and the background count rate in the uranium window varied appreciably from one hole...

  8. Spectrometric techniques 2

    CERN Document Server

    Vanasse, George A

    2013-01-01

    Spectrometric Techniques, Volume II provides information pertinent to vacuum ultraviolet techniques to complete the demonstration of the diversity of methods available to the spectroscopist interested in the ultraviolet visible and infrared spectral regions. This book discusses the specific aspects of the technique of Fourier transform spectroscopy.Organized into five chapters, this volume begins with an overview of the large number of systematic effects in the recording of an interferogram. This text then examines the design approach for a Fourier transform spectrometer with focus on optics.

  9. Determination of effective atomic number of composite materials using backscattered gamma photons - A novel method

    Science.gov (United States)

    Hosamani, M. M.; Badiger, N. M.

    2018-03-01

    The effective atomic number (Zeff) of composite materials has been determined by measuring the backscattered gamma photons at 180°. A 661.6 keV gamma photons from 137Cs radioactive source are allowed to scatter at an angle of 180° from the sample. The backscattered photons at 180° from the sample are detected with "2 × 2″ NaI(Tl) scintillation gamma ray spectrometer coupled to 16 K Multi Channel Analyzer (MCA). It is observed experimentally that the intensity of backscattered photons increases initially with increasing the thickness of the target and then it becomes saturated above a certain thickness. By knowing the saturated thickness values for known atomic number of the elemental targets, the Zeff of composite materials has been determined. The experimentally measured Zeff values have been compared with theoretical values predicted by direct method, power law method and AutoZeff code.

  10. Determination of water diffusion coefficient by gamma radiation and thermal shock

    International Nuclear Information System (INIS)

    Crausse, P.; Lemarchand, D.

    1985-01-01

    Mass transfer coefficient of water in a porous material (baked clay) is determined by gamma ray attenuation (from a Cs135 source) and thermal shock. Water content is found higher by thermal shock, difference obtained between the two methods is discussed. 7 refs [fr

  11. Improved Nearest Neighbor Methods for Gamma Photon Interaction Position Determination in Monolithic Scintillator PET Detectors

    NARCIS (Netherlands)

    van Dam, Herman T.; Seifert, Stefan; Vinke, Ruud; Dendooven, Peter; Lohner, Herbert; Beekman, Freek J.; Schaart, Dennis R.

    2011-01-01

    Monolithic scintillator detectors have been shown to provide good performance and to have various practical advantages for use in PET systems. Excellent results for the gamma photon interaction position determination in these detectors have been obtained by means of the k-nearest neighbor (k-NN)

  12. Determination of Ra-226 by gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Martinez Lobo, A.

    1988-01-01

    This work deals with the method of determination of 226 Ra by low energy photon spectrometry. For this purpose, the interference due to 235 U, that emits a photon with a close energy, has to be considered. The contribution of 235 U to the 186 KeV photopeak is studied through the 63 KeV 234 Th and the 144 KeV 235 U emissions. From the minimum detectable activity of 226 Ra it is discussed the applicability of this method to several kind of samples. (Author)

  13. Estimating $r_{B}^{D\\pi}$ as input to the determination of CKM angle $\\gamma$

    CERN Document Server

    Kenzie, Matthew

    2016-01-01

    The interference between Cabibbo-favoured and Cabibbo-suppressed $B\\to D\\pi$ decay amplitudes provides sensitivity to the CKM angle $\\gamma$. The relative size of the interfering amplitudes is an important ingredient in the determination of $\\gamma$. Using branching fractions from various $B\\to Dh$ decays, and the measured value for $r_{B}^{DK}$, the magnitude of the amplitude ratio of $B^+\\to D^0\\pi^+$ and $B^+\\to \\bar{D}^0\\pi^+$ decays is estimated to be $r_{B}^{D\\pi} = 0.0053 \\pm 0.0007$.

  14. Some energy considerations in gamma ray burst location determinations by an anisotropic array of detectors

    International Nuclear Information System (INIS)

    Young, J.H.

    1986-01-01

    The anisotropic array of detectors to be used in the Burst and Transient Experiment (BATSE) for locating gamma ray burst sources is examined with respect to its ability to locate those sources by means of the relative response of its eight detectors. It was shown that the energy-dependent attenuation effects of the aluminum window covering each detector has a significant effect on source location determinations. Location formulas were derived as a function of detector counts and gamma ray energies in the range 50 to 150 keV. Deviation formulas were derived and serve to indicate the location error that would be cuased by ignoring the influence of the passive absorber

  15. Nomogram for Determining Shield Thickness for Point and Line Sources of Gamma Rays

    Energy Technology Data Exchange (ETDEWEB)

    Joenemalm, C.; Malen, K

    1966-10-15

    A set of nomograms is given for the determination of the required shield thickness against gamma radiation. The sources handled are point and infinite line sources with shields of Pb, Fe, magnetite concrete (p = 3.6), ordinary concrete (p = 2.3) or water. The gamma energy range covered is 0.5 - 10 MeV. The nomograms are directly applicable for source and dose points on the surfaces of the shield. They can easily be extended to source and dose points in other positions by applying a geometrical correction. Also included are data for calculation of the source strength for the most common materials and for fission product sources.

  16. Nomogram for Determining Shield Thickness for Point and Line Sources of Gamma Rays

    International Nuclear Information System (INIS)

    Joenemalm, C.; Malen, K

    1966-10-01

    A set of nomograms is given for the determination of the required shield thickness against gamma radiation. The sources handled are point and infinite line sources with shields of Pb, Fe, magnetite concrete (p = 3.6), ordinary concrete (p = 2.3) or water. The gamma energy range covered is 0.5 - 10 MeV. The nomograms are directly applicable for source and dose points on the surfaces of the shield. They can easily be extended to source and dose points in other positions by applying a geometrical correction. Also included are data for calculation of the source strength for the most common materials and for fission product sources

  17. Determination of plutonium isotopic ratios by using low-energy gamma-ray spectroscopy

    International Nuclear Information System (INIS)

    Li, T.K.

    1983-01-01

    A nondestructive gamma-ray technique has been developed to determine plutonium isotopic ratios. The technique is based on the high-intensity, low-energy gamma rays at 43.48, 45.23, 51.63, 59.54, and 64.83 keV for 238 Pu, 240 Pu, 239 Pu, 241 Am, and 241 Pu, respectively. The results demonstrate that this technique can accurately measure plutonium samples in a timely manner and in a wide range of masses, isotopic contents, chemical forms, and ages from chemical processing

  18. Determination the lethal dose of ascaris lumbricoides ova by gamma irradiation

    CERN Document Server

    Shamma, M A; Sharabi, N

    2002-01-01

    The lethal gamma irradiation dose of ascaris lumbricoides which collected from Damascus Sewage water Plant was determined. Ascaris lumbricoides ova were treated with several gamma irradiation doses with (0.1, 0.2, 0.3, 0.4,...and 1.5 KGy). No morphological changes were observed on the eggs when directly examined microscopically after irradiation. However after two weeks of incubation at 37 degree centigrade the cell contents of the eggs which irradiated with 0.5 KGy and beyond were fragmented and scattered in the whole eggs and no larvae were observed after eight weeks of incubation. It is concluded that the dose 0.5 my be considered as the dose of choice if sewage water is to be treated by gamma rays.

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

    International Nuclear Information System (INIS)

    Diez, B.

    2009-06-01

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

  20. Precise Determination of Silicon in Ceramic Reference Materials by Prompt Gamma Activation Analysis at JRR-3

    Directory of Open Access Journals (Sweden)

    Tsutomu Miura

    2016-04-01

    Full Text Available Prompt gamma activation analysis using a thermal neutron-guided beam at Japan Atomic Energy Agency JRR-3M was applied for the precise determination of Si in silicon nitride ceramic reference materials [Japan Ceramic Reference Material (JCRM R 003]. In this study, the standard addition method coupled with internal standard was used for the nondestructive determination of Si in the sample. Cadmium was used as internal standard to obtain the linear calibration curves and to compensate for the neutron beam variability. The analytical result of determining Si in JCRM R 003 silicon nitride fine powder ceramic reference materials using prompt gamma activation analysis was in good agreement with that obtained by classical gravimetric analysis. The relative expanded measurement uncertainty (k = 2 associated with the determined value was 2.4%.

  1. Determining Some Parameters Of Uranium Material By GAMMA Spectrometry Using Intrinsic Efficiency Calibration

    International Nuclear Information System (INIS)

    Le Tuan Anh; Bui Minh Hue; Bui Van Loat; Nguyen Cong Tam

    2011-01-01

    Abundance and age of uranium material are two significant parameters. Traditionally, they are determined by alpha spectrometry and mass-spectrometry, which are destructive methods. In this report, we exhibit the result of abundance and age, which were determined by gamma-spectrometry using intrinsic efficiency calibration. This is a nondestructive method without using standard source or any reference samples, and applicable to material of any geometrical shape. The result obtained is in good agreement with the results obtained by other authors. (author)

  2. Design and construction of prompt-gamma spectroscopy facility applied to the boron determination

    International Nuclear Information System (INIS)

    Poblete, Victor; Henriquez, Carlos; Klein, Juan; Navarro, Gustavo

    1996-01-01

    A prompt-gamma spectroscopy facility was developed using the south tangential neutron beam of the RECH-1 research reactor for boron determination. The implementation of a thermal neutron beam was performed considering different aspects such as biological protection of working area and the beam collimation for a Ge detector, design and sample holder selection, standards and sample preparation. One ppm of Boron in different samples with counting-rate of 20 minutes and a good accuracy were determined. (author)

  3. A model independent determination of the B{yields}X{sub s}{gamma} decay rate

    Energy Technology Data Exchange (ETDEWEB)

    Bernlochner, Florian U. [Victoria Univ., BC (Canada); Lacker, Heiko [Humboldt-Universitaet, Berlin (Germany); Ligeti, Zoltan [California Univ., Berkeley, CA (United States). Ernest Orlando Lawrence Berkeley National Laboratory; Stewart, Iain W. [Massachusetts Institute of Technology, Cambridge, MA (United States). Center for Theoretical Physics; Tackmann, Frank J.; Tackmann, Kerstin [Deutsches Elektronen-Synchrotron (DESY), Hamburg (Germany)

    2013-03-15

    The goal of the SIMBA collaboration is to provide a global fit to the available measurements of inclusive B{yields}X{sub s}{gamma} and B{yields}X{sub u}l{nu} decays. By performing a global fit one is able to simultaneously determine the relevant normalizations, i.e. the total B{yields}X{sub s}{gamma} rate and the CKM-matrix element vertical stroke Vub vertical stroke, together with the required hadronic parameters, most importantly the b-quark mass and the b-quark distribution function in the B-meson, called the shape function. In this talk, the current status on the model-independent determination of the shape function and vertical stroke C{sub 7}{sup incl}V{sub tb}V{sub ts}{sup *} vertical stroke, which parametrizes the total B{yields}X{sub s}{gamma} rate, from a global fit to the available B{yields}X{sub s}{gamma} measurements from Babar and Belle is presented. In particular, the theoretical uncertainties originating from variations of the different factorization scales are evaluated.

  4. Matrix effects in the determination of phosphorus and sodium by proton-induced prompt gamma spectrometry

    International Nuclear Information System (INIS)

    Olivier, C.; Morland, H.J.

    1990-01-01

    By measuring the yield of prompt gamma rays, induced by accelerated charged particles, the ratio of the ranges in sample and standard can be used in the average cross-section method to determine elemental or isotopic compositions. By spiking the sample with a known amount of a compound containing a non-analyte element (absent in the sample), the appropriate range in the sample can be determined by measuring the prompt gamma rays induced in the non-analyte spike. With lithium compounds as the non-analyte spike, sodium and phosphorus were determined in ivory. The method was tested by analysing the standard reference materials SRM 91, SRM 120c, and SRM 694. 2 figs., 5 tabs., 10 refs

  5. Advanced gamma spectrum processing technique applied to the analysis of scattering spectra for determining material thickness

    International Nuclear Information System (INIS)

    Hoang Duc Tam; VNUHCM-University of Science, Ho Chi Minh City; Huynh Dinh Chuong; Tran Thien Thanh; Vo Hoang Nguyen; Hoang Thi Kieu Trang; Chau Van Tao

    2015-01-01

    In this work, an advanced gamma spectrum processing technique is applied to analyze experimental scattering spectra for determining the thickness of C45 heat-resistant steel plates. The single scattering peak of scattering spectra is taken as an advantage to measure the intensity of single scattering photons. Based on these results, the thickness of steel plates is determined with a maximum deviation of real thickness and measured thickness of about 4 %. Monte Carlo simulation using MCNP5 code is also performed to cross check the results, which yields a maximum deviation of 2 %. These results strongly confirm the capability of this technique in analyzing gamma scattering spectra, which is a simple, effective and convenient method for determining material thickness. (author)

  6. Using gamma distribution to determine half-life of rotenone, applied in freshwater

    International Nuclear Information System (INIS)

    Following the use of rotenone to eradicate invasive pest fish, a dynamic first-order kinetic model is usually used to determine the half-life and rate at which rotenone dissipated from the treated waterbody. In this study, we investigate the use of a stochastic gamma model for determining the half-life and rate at which rotenone dissipates from waterbodies. The first-order kinetic and gamma models produced similar values for the half-life (4.45 days and 5.33 days respectively) and days to complete dissipation (51.2 days and 52.48 days respectively). However, the gamma model fitted the data better and was more flexible than the first-order kinetic model, allowing us to use covariates and to predict a possible range for the half-life of rotenone. These benefits are particularly important when examining the influence that different environmental factors have on rotenone dissipation and when trying to predict the rate at which rotenone will dissipate during future operations. We therefore recommend that in future the gamma distribution model is used when calculating the half-life of rotenone in preference to the dynamic first-order kinetics model. - Highlights: • We investigated the use of the gamma model to calculate the half-life of rotenone. • Physical and environmental variables can be incorporated into the model. • A method for calculating the range around a mean half-life is presented. • The model is more flexible than the traditionally used first-order kinetic model

  7. Comparison of three spectrophotometric methods for the determination of gamma-oryzanol in rice bran oil.

    Science.gov (United States)

    Bucci, Remo; Magrì, Andrea D; Magrì, Antonio L; Marini, Federico

    2003-04-01

    A comparison of the results obtained by applying three spectrophotometric methods (at fixed wavelength, second-derivative and multicomponent analysis) to the determination of gamma-oryzanol in rice bran oil is reported. At fixed wavelength the results are more accurate when using isopropyl alcohol, rather than n-heptane, to dilute the oil samples, because the absorption bands of gamma-oryzanol are red-shifted and the absorbance, measured at lambda(max)=327 nm, is less affected by the interference of the oil "matrix" (lambda(max)=314 nm in n-heptane).However, to obtain accurate results also in oils with a low content of gamma-oryzanol, it is necessary to perform the analysis using second-derivative ((2)D330.365) or multicomponent (lambda=310-360 nm) methods. The first one fully removes the interference of oil matrix whilst the second, which needs a specific computational program to process the spectrophotometric data, furnishes evidence the presence of some unexpected interference in the analysis and/or standards which are not representative of the analysed samples, from the square root of the sum of the squared differences at each point between the linear combination of the standards and the unknown spectra (RMS error).Finally, some aspects of the chemical, spectroscopic (UV, IR) and thermoanalytical (TG, DSC) behaviour of gamma-oryzanol and the values of the parameters which enable "computation" of its UV spectra are reported.

  8. Hydraulic conductivity determination of a dark red latosol by gamma attenuation and tensiometry

    International Nuclear Information System (INIS)

    Oliveira, Julio Cesar Martins de; Reichardt, Klaus; Costa, Antonio Carlos Saraiva da

    1995-01-01

    Results for the hydraulic conductivity of a dark red latosol (Oxisol) under laboratory and field conditions are presented. The laboratory experiments simulated field conditions through the measurement of the soil water content profiles as a function of time in soil columns. The data were obtained by the 241 Am gamma-ray transmission method, using standard gamma ray spectrometry equipment. Tensiometers at the depths of 10 and 25 cm were used to obtain the soil water content profiles as a function of time in the field experiments. The hydraulic conductivity functions were determined through internal soil drainage. The results showed higher values of the hydraulic conductivity measured in the field, compared with the laboratory values. The hydraulic conductivity determination methods presented distinct values for the field experiments as well as for the laboratory ones. (author)

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

    International Nuclear Information System (INIS)

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

    1975-12-01

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

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

    Science.gov (United States)

    Hizem, N; Ben Fredj, A; 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.

  11. STUDY CONCERNING THE POSSIBILITY OF GAMMA-SPECTROSCOPY METHOD TO DETERMINE THE TOTAL POTASSIUM IN SOILS

    Directory of Open Access Journals (Sweden)

    Tamara Leah

    2011-12-01

    Full Text Available It was proved the possibility of determination the total potassium in soils by gamma-spectroscopic method with subsequent calculation of total potassium content in according to value of 40K isotope (expressed in Becquerel, Bq, using the formula: К2О, % = С . А, where: C – conversion coefficient, A – activity of isotope 40K in soil, Bq/kg. Conversion coefficient for chernozems of Moldova – C=0,00337.

  12. Power and combustion rate determination of irradiated nuclear fuels at Osiris by in pile gamma spectrometry

    International Nuclear Information System (INIS)

    Musso, J.F.

    1976-01-01

    The OSIRIS reactor is a particularly well suited tool for the study of the various types of reactors, either in normal operation or under emergency conditions. Among the reference parameters which allow a comparison between irradiation conditions in an experimental and a power reactor, the specific burn-up and the power are of importance. until now, no single method of power and burn up measurement could give simultaneously precise results and fast measurements without destroying the fuel itself. Hence the incentive to make use of in-pile gamma fuel scanning to provide an overall answer to these questions. Chapter 1 reviews the most important experimental methods of determination of the specific burn up and of irradiation power and a summary of the principles of in-pile gamma fuel scanning. Chapter 2 describes the tools, the calculation programs and the experimental apparatus used in this study. Chapter 3 is concerned with the determination of the specific burn up using in-pile gamma fuel scanning. Chapter 4 describes the method of determination of the irradiation power and gives the first experimental results [fr

  13. Quantitative determination of plant phenolics in Urtica dioica extracts by high-performance liquid chromatography coupled with tandem mass spectrometric detection.

    Science.gov (United States)

    Orčić, Dejan; Francišković, Marina; Bekvalac, Kristina; Svirčev, Emilija; Beara, Ivana; Lesjak, Marija; Mimica-Dukić, Neda

    2014-01-15

    A method for quantification of 45 plant phenolics (including benzoic acids, cinnamic acids, flavonoid aglycones, C- and O-glycosides, coumarins, and lignans) in plant extracts was developed, based on reversed phase HPLC separation of extract components, followed by tandem mass spectrometric detection. The phenolic profile of 80% MeOH extracts of the stinging nettle (Urtica dioica L.) herb, root, stem, leaf and inflorescence was obtained by using this method. Twenty-one of the investigated compounds were present at levels above the reliable quantification limit, with 5-O-caffeoylquinic acid, rutin and isoquercitrin as the most abundant. The inflorescence extracts were by far the richest in phenolics, with the investigated compounds amounting 2.5-5.1% by weight. As opposed to this, the root extracts were poor in phenolics, with only several acids and derivatives being present in significant amounts. The results obtained by the developed method represent the most detailed U. dioica chemical profile so far. Copyright © 2013 Elsevier Ltd. All rights reserved.

  14. Determination of gold in lump by the gamma-activation analysis method

    International Nuclear Information System (INIS)

    Yantsen, V.A.; Ermakov, K.S.

    2006-01-01

    Full text: In the report the installation is described used in the Central gamma-activation analysis laboratory (CGAAL) for express quantitative determination of gold concentration in large powdered samples. The method of gold contents determination for non-crushed samples (pieces up to 100 mm). The given gamma-activation analysis method is widely used in mining industry, and at researches related with selection of optimal technological circuits designed for sorting the pieces of ore and rock materials. By developing this method it is now possible to create the technological collection of separated pieces by size, large by the amount of samples, imitating various sorts (by gold concentration in them) and types (by elemental composition) ores, and, based on these collection, to compare the efficiencies of various enrichment methods by knowing in advance the concentrations of gold in these lumps being the final sorting products. The Gamma-activation analysis method of large pieces is mainly used as foundation for the x-ray radiometric (XRR) method of pieces separation of gold-bearing ores from the deposits mined by the Navoi mining combine. It allows significant increase in the rate of research and development works on selection of the most reliable separation characteristics. Based on these one can develop optimal technological circuits for ore enrichment with portion sorting methods. (author)

  15. Determination of nuclear fuel burnup by non-destructive gamma spectroscopy

    International Nuclear Information System (INIS)

    Soares, A.J.

    1979-01-01

    The determination of nuclear fuel burnup by the non-destructive gamma spectroscopy method is studied. A MTR (Materials Testing Reactor) -type fuel element is used in the measurement. The fuel element was removed from the reactor core in 1958 and, because of the long decay time, show only one peak in is gamma spectrum at 661.6 Kev. Corresponding to 137 Cs. Measurements are made at 330 points of the element using a Nal detector and the final result revealed that the quantity of 235 U consumed was 3.3 +- 0,8 milligram in the entire element. The effect of the migration of 137 Cs in the element is neglected in view of the fact that it occurs only when the temperature is above 1000 0 C, which is not the case in IEAR-1. (Author)

  16. Determination of gross gamma and gross beta activities in liquid effluent samples. Phase I

    International Nuclear Information System (INIS)

    Curtis, K.E.; Sood, S.P.

    1985-08-01

    Several inadequacies in the presently used procedures for gross gamma and gross beta measurements in aqueous wastes have been identified. Both the presence of suspended particulate activity and the use of cesium-137 as a calibration standard can cause gross gamma measurements to overestimate the actual activity in the sample. At the same time, sample preparation for the determination of gross beta activities causes large losses of radioiodine before the measurement step and the presence of solid material can cause a serious decrease in the beta counting efficiency. A combination of these errors could result in large discrepancies between the results obtained by the two measurement methods. Improved procedures are required to overcome these problems

  17. Determination of the 4 mm Gamma Knife helmet relative output factor using a variety of detectors

    International Nuclear Information System (INIS)

    Tsai, J.-S.; Rivard, Mark J.; Engler, Mark J.; Mignano, John E.; Wazer, David E.; Shucart, William A.

    2003-01-01

    Though the 4 mm Gamma Knife helmet is used routinely, there is disagreement in the Gamma Knife users community on the value of the 4 mm helmet relative output factor. A range of relative output factors is used, and this variation may impair observations of dose response and optimization of prescribed dose. To study this variation, measurements were performed using the following radiation detectors: silicon diode, diamond detector, radiographic film, radiochromic film, and TLD cubes. To facilitate positioning of the silicon diode and diamond detector, a three-dimensional translation micrometer was used to iteratively determine the position of maximum detector response. Positioning of the films and TLDs was accomplished by manufacturing custom holders for each technique. Results from all five measurement techniques indicate that the 4 mm helmet relative output factor is 0.868±0.014. Within the experimental uncertainties, this value is in good agreement with results obtained by other investigators using diverse techniques

  18. Determination of Th and U by neutron activation for gamma spectrometry calibration in situ

    International Nuclear Information System (INIS)

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

    2012-10-01

    Using the analysis by neutron activation to determine the profile of the thorium and uranium concentration calibration factors were obtained for their use in the gamma spectrometry in situ. Three sites were selected (San Ramon, Villa de Cos y la Zacatecana) and the analysis by activation was development in the Laboratory of Nuclear Engineering Teaching of the Texas University in Austin with the nuclear reactor Ut-TRIGA. Starting from the gamma spectra in situ, the areas of normalized photo-pick of the radioisotopes were: 208 Tl and 228 Ac for the thorium series and 214 Pb and 214 Bi for the uranium series. The averages of the factors found in units of (cpm/Bq/Kg) are of 105.63±8.32 and 75.87±4.61 for the thorium and uranium, respectively. (Author)

  19. Fluorine determination in human and animal bones by particle-induced gamma-ray emission

    International Nuclear Information System (INIS)

    Sastri, Chaturvedula S.; Hoffmann, Peter; Ortner, Hugo M.; Iyengar, Venkatesh; Blondiaux, Gilbert; Tessier, Yves; Petri, Hermann; Aras, Namik K.; Zaichick, Vladimir

    2002-01-01

    Fluorine was determined in the iliac crest bones of patients and in ribs collected from postmortem investigations by particle-induced gamma-ray emission based on the 19 F(p,pγ) 19 F reaction, using 20/2.5 MeV protons. The results indicate that for 68% of the human samples the F concentration is in the range 500-1999 μg g -1 . For comparison purposes fluorine was also determined in some animal bones; in some animal tissues lateral profiles of fluorine were measured. (abstract)

  20. Reimiep 87. An interlaboratory U-235 enrichment determination by gamma measurement on solid UF6 sample

    International Nuclear Information System (INIS)

    Aparo, M.; Cresti, P.

    1988-01-01

    Gamma spectroscopy technique, based on the measurement of U 235 186 KeV flux, is now currently used for the determination of Uranium enrichment in different material of nuclear fuel cycle, namely: Uranium metallic, UO 2 pellets, UF 6 liquid or solid. The present paper describes the use of such a technique and the obtained results in determining the U 235 /U atomic isotopic abundance on a certified UF 6 solid sample. The measurements have been carried out in the frame work of the partecipation to the ''UF 6 Interlaboratory Measurements Evaluation Programme'' organized by CBNM/Geel with the support of the ESARDA (European Safeguards Research and Development Association)

  1. V gamma 9V delta 2 T-cell anergy and complementarity-determining region 3-specific depletion during paroxysm of nonendemic malaria infection.

    Science.gov (United States)

    Martini, Federico; Paglia, Maria Grazia; Montesano, Carla; Enders, Patrick J; Gentile, Marco; Pauza, C David; Gioia, Cristiana; Colizzi, Vittorio; Narciso, Pasquale; Pucillo, Leopoldo Paolo; Poccia, Fabrizio

    2003-05-01

    V gamma 9V delta 2 T lymphocytes strongly respond to phosphoantigens from Plasmodium parasites. Thus, we analyzed the changes in V gamma 9V delta 2 T-cell function and repertoire during the paroxysm phase of nonendemic malaria infection. During malaria paroxysm, V gamma 9V delta 2 T cells were early activated but rapidly became anergic and finally loose J gamma 1.2 V gamma 9 complementarity-determining region 3 transcripts.

  2. Water quality - Determination of the activity concentration of radionuclides - Method by high resolution gamma-ray spectrometry. 2. ed.

    International Nuclear Information System (INIS)

    2007-01-01

    This International Standard allows (after proper sampling, sample handling and, when necessary or desirable, sample preparation) the simultaneous determination of the activity concentration of several gamma-ray emitting radionuclides in water samples by gamma-ray spectrometry using high purity germanium [HPGe] detectors. Gamma-ray emitting radionuclides are widespread both as naturally occurring and as man-made radionuclides. Therefore, environmental samples usually contain a multitude of different gamma-ray emitters and high resolution gamma-ray spectrometry provides a useful analytical tool for environmental measurements. Gamma rays cause electron-hole pairs when interacting with matter. When a voltage is applied across a semiconductor detector, these electron hole-pairs are, after proper amplification, detected as current pulses. The pulse height is related to the energy absorbed from the gamma-photon or photons in the resolving time of the detector and electronics. By discriminating between the height of the pulses, a gamma-ray pulse height spectrum is obtained. After analysis of the spectrum, the various peaks are assigned to the radionuclides which emitted the corresponding gamma rays using the previously obtained energy detector calibration. The concentration of the radionuclides present in the sample is calculated using the previously obtained energy dependent detector efficiency. The paper provides information on scope, normative references, terms and conditions, symbols and units, principle, reference sources, reagents, gamma spectrometry equipment, sampling, procedure, expression of results and test report followed by Annex A (Example of a carrier solution which can be added to the water sample when waste water from a nuclear power plant is investigated), Annex B (Calculation of the activity concentration from a gamma spectrum using a linear background subtraction (undisturbed peak) and a bibliography

  3. sup 2 sup 1 sup 0 Pb determination by gamma spectrometry in voluminal samples (cylindrical geometry)

    CERN Document Server

    San Miguel, E G; Bolivar, J P; Garcia-Tenorio, R; Martin, J E

    2002-01-01

    In this paper a simple method for the direct analysis of sup 2 sup 1 sup 0 Pb (T sub 1 sub / sub 2 =22.3 years) by gamma-ray spectrometry in sediment samples with coaxial Ge detectors is outlined. This method, developed for a cylindrical sample geometry, accounts for variable sample heights and provides a fundamental advantage: individual self-absorption corrections can easily be determined knowing the apparent densities of the samples. The results obtained with the proposed method are in good agreement with those given by other techniques.

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

    International Nuclear Information System (INIS)

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

    1978-01-01

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

  5. Prompt gamma-ray activation analysis for determination of boron in aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Baechler, S. E-mail: sebastien.beachler@unifr.ch; Kudejova, P.; Jolie, J.; Schenker, J.-L.; Stritt, N

    2002-08-01

    Prompt gamma-ray activation analysis (PGAA) is a nuclear analytical technique for the determination of trace and other elements in solid, liquid or gaseous samples. The method consists in observing gamma rays emitted by a sample during neutron irradiation. Of particular importance for PGAA is the measurement of boron. Indeed, this technique gives the opportunity to detect boron concentration down to the ppm or ppb level depending on the sample matrix. Furthermore, boron cannot be easily measured by other methods without risks of contamination. Trace analysis of boron in liquids has been performed and characterized at the PGA facility of the neutron spallation source SINQ (Paul Scherrer Institute, Switzerland). First, a calibration curve was determined with standard boron solutions. Then, the PGAA was applied for the determination of boron in geological water samples. The results were compared with ICP-MS measurements. Finally, the method yielded promising results to measure the concentration of boron taken up by cells in a new treatment for rheumatoid arthritis.

  6. GammaWorkshops Proceedings

    Energy Technology Data Exchange (ETDEWEB)

    Ramebaeck, H. (ed.) (Swedish Defence Research Agency (Sweden)); Straalberg, E. (Institute for Energy Technology, Kjeller (Norway)); Klemola, S. (Radiation and Nuclear Safety Authority, STUK (Finland)); Nielsen, Sven P. (Technical Univ. of Denmark. Risoe National Lab. for Sustainable Energy, Roskilde (Denmark)); Palsson, S.E. (Icelandic Radiation Safety Authority (Iceland))

    2012-01-15

    Due to a sparse interaction during the last years between practioners in gamma ray spectrometry in the Nordic countries, a NKS activity was started in 2009. This GammaSem was focused on seminars relevant to gamma spectrometry. A follow up seminar was held in 2010. As an outcome of these activities it was suggested that the 2011 meeting should be focused on practical issues, e.g. different corrections needed in gamma spectrometric measurements. This three day's meeting, GammaWorkshops, was held in September at Risoe-DTU. Experts on different topics relevant for gamma spectrometric measurements were invited to the GammaWorkshops. The topics included efficiency transfer, true coincidence summing corrections, self-attenuation corrections, measurement of natural radionuclides (natural decay series), combined measurement uncertainty calculations, and detection limits. These topics covered both lectures and practical sessions. The practical sessions included demonstrations of tools for e.g. corrections and calculations of the above meantioned topics. (Author)

  7. Molecular sizes of lichen ice nucleation sites determined by gamma radiation inactivation analysis

    International Nuclear Information System (INIS)

    Kieft, T.L.; Ruscetti, T.

    1992-01-01

    It has previously been shown that some species of lichen fungi contain proteinaceous ice nuclei which are active at temperatures as warm as −2 °C. This experiment was undertaken to determine the molecular sizes of ice nuclei in the lichen fungus Rhizoplaca chrysoleuca and to compare them to bacterial ice nuclei from Pseudomonas syringae. Gamma radiation inactivation analysis was used to determine molecular weights. Radiation inactivation analysis is based on target theory, which states that the likelihood of a molecule being inactivated by gamma rays increases as its size increases. Three different sources of ice nuclei from the lichen R. chrysoleuca were tested: field-collected lichens, extract of lichen fungus, and a pure culture of the fungus R. chrysoleuca. P. syringae strain Cit7 was used as a source of bacterial ice nuclei. Samples were lyophilized, irradiated with gamma doses ranging from 0 to 10.4 Mrads, and then tested for ice nucleation activity using a droplet-freezing assay. Data for all four types of samples were in rough agreement; sizes of nucleation sites increased logarithmically with increasing temperatures of ice nucleation activity. Molecular weights of nucleation sites active between −3 and −4 °C from the bacteria and from the field-collected lichens were approximately 1.0 × 10 6 Da. Nuclei from the lichen fungus and in the lichen extract appeared to be slightly smaller but followed the same log-normal pattern with temperature of ice nucleation activity. The data for both the bacterial and lichen ice nuclei are in agreement with ice nucleation theory which states that the size of ice nucleation sites increases logarithmically as the temperature of nucleation increases linearly. This suggests that although some differences exist between bacterial and lichen ice nucleation sites, their molecular sizes are quite similar

  8. Analytical procedure for the radiometric determination of uranium in ores

    International Nuclear Information System (INIS)

    Bone, S.J.; Porritt, R.E.J.

    1976-06-01

    Two methods are described for the non-destructive determination of uranium in ores: a beta-gamma measuring method and a gamma-spectrometrical one. The first has the advantage that the analysis is not influenced by a radioactive unbalance in the sample (say by loss of radium as a result of chemical decomposition of the ores) and that it can be carried out with comparitively simple apparative expenditure. It is, however, relatively inaccurate (+-25%) and should only be used as a surveying method. The gamma-spectrometrical analysis (accuracy about +-10%) gives information about an unbalance present between U 238 and Ra 226 and thus enables an appropriate correction to be made. A thorium contribution with its decay products can also be corrected. (RB) [de

  9. Conductometry, spectrophotometry and mass spectrometric ...

    African Journals Online (AJOL)

    ... versus the mole ratio of [AZT]/[M2+], Job's method of continuous variation and mole ratio method showed the stoichiometry to be 1:1 (M2+:AZT) for both the cations. The metal ion-AZT complexes formed through the nitrogen of the azide group were further ascertained by liquid chromatography-mass spectrometric analysis.

  10. NZG 201 portable spectrometric unit

    International Nuclear Information System (INIS)

    Jursa, P.; Novakova, O.; Slezak, V.

    The NZG 201 spectrometric unit is a portable single-channel processing unit supplied from the mains or a battery which allows the qualitative and quantitative measurement of different types of ionizing radiation when connected to a suitable detection unit. The circuit layout and the choice of control elements makes the spectrometric unit suitable for use with scintillation detector units. The spectrometric unit consists of a pulse amplifier, an amplitude pulse analyzer, a pulse counter, a pulse rate counter with an output for a recorder, a high voltage source and a low voltage source. The block diagram is given. All circuits are modular and are mounted on PCB's. The apparatus is built in a steel cabinet with a raised edge which protects the control elements. The linear pulse amplifier has a maximum gain of 1024, the pulse counter has a maximum capacity of 10 6 -1 imp and time resolution better than 0.5 μs. The temperature interval at which the apparatus is operational is 0 to 45 degC, its weight is 12.5 kg and dimensions 36x280x310 mm, energy range O.025 to 2.5 MeV, for 137 Cs the energy resolution is 8 to 10%. The spectrometric unit NZG 2O1 may, with regard to its parameters, number and range of control elements, be used as a universal measuring unit. (J.P.)

  11. Determination of aminopolycarboxylic acids in river water by solid-phase extraction on activated charcoal cartridges and gas chromatography with mass spectrometric detection. Method performance characteristics and estimation of the uncertainty.

    Science.gov (United States)

    Jiménez, Juan J

    2013-04-03

    A new sample preparation procedure to determine aminopolycarboxylic acids (ethylenediaminetetraacetic acid, EDTA, nitrilotriacetic acid, NTA, diethylenetriaminepentaacetic acid, DTPA, and cyclohexanediaminetetraacetic acid, CDTA) in river water is described. The procedure consists of the solid-phase extraction of the aminopolycaroxyllic acids on activated charcoal cartridges after increasing the ionic strength and acidifying the sample. The extract was eluted with methanol and the analytes were methylated in presence of BF3/methanol to determine them by GC with mass spectrometric detection. Recoveries were higher than 90% with good repeatabilities and inter-day precision for concentrations close to quantification limits (about 10 μg L(-1)) and higher. It has been verified that the proposed method is robust according to the Youden and Steiner test and free of matrix effects arisen from the presence of organic matter and iron(III) as deduced from statistical tests. A bottom-up approach was followed to estimate the uncertainty of the measured concentration. At concentrations close to 10 μg L(-1) the most relevant step of the method is the calculus of the interpolated concentration which has a high value of relative standard uncertainty. Copyright © 2013 Elsevier B.V. All rights reserved.

  12. Determination of {sup 7}BE in soil sample by gamma spectrometry for erosion researchs

    Energy Technology Data Exchange (ETDEWEB)

    Esquivel, Alexander D., E-mail: alexander.esquivel@utp.ac.pa [Centro de Investigaciones Hidraulicas e Hidrotecnicas (CIHH/UTP-PA), Universidad Tecnologica de Panama (Panama); Kastner, Geraldo F.; Amaral, Angela M.; Monteiro, Roberto Pellacani G.; Moreira, Rubens M., E-mail: gfk@cdtn.br, E-mail: ama@cdtn.br, E-mail: rpgm@cdtn.br, E-mail: rubens@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2015-07-01

    Cosmogenic {sup 7}Be is a natural radiotracer produced in the stratosphere and troposphere and reached to the Earth surface via wet and dry fallout and hence its measurement for research of erosion in soils is very significant. The {sup 7}Be radio analyse based on gamma spectrometry technique has been a routine methodology for decades and although is the reference procedure is not free of analytical interference. {sup 7}Be is a β-γ emitting radionuclide (Eγ = 477.59 keV, T½ = 53.12d) and depending on the chemical profile of the soil its determination is susceptible to {sup 228}Ac (E{sub γ} = 478.40 keV, T½ = 6.15h) interference. The aim of this work was to establish an analytical protocol for the {sup 7}Be determination in soil samples from Juatuba-Mg region in different sampling periods of dry and rainy seasons for erosion studies and to establish some methodologies for evaluating and correcting the interference level of {sup 228}Ac in the {sup 7}Be activity measurements by gamma spectrometry. (author)

  13. Spectrometric properties and radiation damage of BGO crystals

    Science.gov (United States)

    Kim, Gen C.; Gasanov, Eldar M.

    1997-07-01

    Spectrometric properties, such as light output, energy resolution BGO crystals before and after (superscript 60)Co gamma-ray (dose 10(superscript 4) - 10(superscript 6) R) and neutron irradiation (fluence 10(superscript 14) cm(superscript -2)) are investigated. Condition for degradation of spectrometric properties and their recovering after irradiation are studied. The energy spectrum of the photons emitted from BGO crystals irradiated with neutron fluence contains the long living background peak which is caused by self-irradiation with radioactive isotopes produced in the crystals. The defect production was studied in crystals under the high dose gamma-irradiation with (superscript 60)Co isotope. It was found that after doses above 10(superscript 8) R the color center at 365 nm and doses higher than 10(superscript 9) R a wide absorption band in the region of 300 - 350 nm occur. Comparison of these results with those of reactor irradiation has shown that under the high dose gamma-irradiation the structure defect production takes place.

  14. Determination of the LEP centre-of-mass energy from Z$\\gamma$ events

    CERN Document Server

    Barate, R.; Ghez, Philippe; Goy, C.; Jezequel, S.; Lees, J.P.; Martin, F.; Merle, E.; Minard, M.N.; Pietrzyk, B.; Przysiezniak, H.; Alemany, R.; Casado, M.P.; Chmeissani, M.; Crespo, J.M.; Fernandez, E.; Fernandez-Bosman, M.; Garrido, L.; Grauges, E.; Juste, A.; Martinez, M.; Merino, G.; Miquel, R.; Mir, L.M.; Morawitz, P.; Pacheco, A.; Park, I.C.; Riu, I.; Colaleo, A.; Creanza, D.; De Palma, M.; Iaselli, G.; Maggi, G.; Maggi, M.; Nuzzo, S.; Ranieri, A.; Raso, G.; Ruggieri, F.; Selvaggi, G.; Silvestris, L.; Tempesta, P.; Tricomi, A.; Zito, G.; Huang, X.; Lin, J.; Ouyang, Q.; Wang, T.; Xie, Y.; Xu, R.; Xue, S.; Zhang, J.; Zhang, L.; Zhao, W.; Abbaneo, D.; Becker, U.; Boix, G.; Cattaneo, M.; Cerutti, F.; Ciulli, V.; Dissertori, G.; Drevermann, H.; Forty, R.W.; Frank, M.; Gianotti, F.; Greening, T.C.; Halley, A.W.; Hansen, J.B.; Harvey, John; Janot, P.; Jost, B.; Lehraus, I.; Leroy, O.; Loomis, C.; Maley, P.; Mato, P.; Minten, A.; Moutoussi, A.; Ranjard, F.; Rolandi, Gigi; Schlatter, D.; Schmitt, M.; Schneider, O.; Spagnolo, P.; Tejessy, W.; Teubert, F.; Tomalin, I.R.; Tournefier, E.; Wright, A.E.; Ajaltouni, Z.; Badaud, F.; Chazelle, G.; Deschamps, O.; Dessagne, S.; Falvard, A.; Ferdi, C.; Gay, P.; Guicheney, C.; Henrard, P.; Jousset, J.; Michel, B.; Monteil, S.; Montret, J.C.; Pallin, D.; Perret, P.; Podlyski, F.; Hansen, J.D.; Hansen, J.R.; Hansen, P.H.; Nilsson, B.S.; Rensch, B.; Waananen, A.; Daskalakis, G.; Kyriakis, A.; Markou, C.; Simopoulou, E.; Vayaki, A.; Blondel, A.; Brient, J.C.; Machefert, F.; Rouge, A.; Swynghedauw, M.; Tanaka, R.; Valassi, A.; Videau, H.; Focardi, E.; Parrini, G.; Zachariadou, K.; Cavanaugh, R.; Corden, M.; Georgiopoulos, C.; Antonelli, A.; Bencivenni, G.; Bologna, G.; Bossi, F.; Campana, P.; Capon, G.; Chiarella, V.; Laurelli, P.; Mannocchi, G.; Murtas, F.; Murtas, G.P.; Passalacqua, L.; Pepe-Altarelli, M.; Chalmers, M.; Curtis, L.; Lynch, J.G.; Negus, P.; O'Shea, V.; Raeven, B.; Raine, C.; Smith, D.; Teixeira-Dias, P.; Thompson, A.S.; Ward, J.J.; Buchmuller, O.; Dhamotharan, S.; Geweniger, C.; Hanke, P.; Hansper, G.; Hepp, V.; Kluge, E.E.; Putzer, A.; Sommer, J.; Tittel, K.; Werner, S.; Wunsch, M.; Beuselinck, R.; Binnie, D.M.; Cameron, W.; Dornan, P.J.; Girone, M.; Goodsir, S.; Marinelli, N.; Martin, E.B.; Nash, J.; Nowell, J.; Sciaba, A.; Sedgbeer, J.K.; Thomson, Evelyn J.; Williams, M.D.; Ghete, V.M.; Girtler, P.; Kneringer, E.; Kuhn, D.; Rudolph, G.; Bowdery, C.K.; Buck, P.G.; Ellis, G.; Finch, A.J.; Foster, F.; Hughes, G.; Jones, R.W.L.; Robertson, N.A.; Smizanska, M.; Williams, M.I.; Giehl, I.; Holldorfer, F.; Jakobs, K.; Kleinknecht, K.; Krocker, M.; Muller, A.S.; Nurnberger, H.A.; Quast, G.; Renk, B.; Rohne, E.; Sander, H.G.; Schmeling, S.; Wachsmuth, H.; Zeitnitz, C.; Ziegler, T.; Aubert, J.J.; Benchouk, C.; Bonissent, A.; Carr, J.; Coyle, P.; Ealet, A.; Fouchez, D.; Motsch, F.; Payre, P.; Rousseau, D.; Talby, M.; Thulasidas, M.; Tilquin, A.; Aleppo, M.; Antonelli, M.; Gilardoni, Simone S.; Ragusa, F.; Buescher, Volker; Dietl, H.; Ganis, G.; Huttmann, K.; Lutjens, G.; Mannert, C.; Manner, W.; Moser, H.G.; Schael, S.; Settles, R.; Seywerd, H.; Stenzel, H.; Wiedenmann, W.; Wolf, G.; Azzurri, P.; Boucrot, J.; Callot, O.; Chen, S.; Davier, M.; Duflot, L.; Grivaz, J.F.; Heusse, P.; Jacholkowska, A.; Kado, M.; Lefrancois, J.; Serin, L.; Veillet, J.J.; Videau, I.; de Viviede Regie, J.B.; Zerwas, D.; Bagliesi, Giuseppe; Bettarini, S.; Boccali, T.; Bozzi, C.; Calderini, G.; Dell'Orso, R.; Ferrante, I.; Giassi, A.; Gregorio, A.; Ligabue, F.; Lusiani, A.; Marrocchesi, P.S.; Messineo, A.; Palla, F.; Rizzo, G.; Sanguinetti, G.; Sguazzoni, G.; Tenchini, R.; Vannini, C.; Venturi, A.; Verdini, P.G.; Blair, G.A.; Coles, J.; Cowan, G.; Green, M.G.; Hutchcroft, D.E.; Jones, L.T.; Medcalf, T.; Strong, J.A.; von Wimmersperg-Toeller, J.H.; Botterill, D.R.; Clifft, R.W.; Edgecock, T.R.; Norton, P.R.; Thompson, J.C.; Bloch-Devaux, Brigitte; Colas, P.; Fabbro, B.; Faif, G.; Lancon, E.; Lemaire, M.C.; Locci, E.; Perez, P.; Rander, J.; Renardy, J.F.; Rosowsky, A.; Trabelsi, A.; Tuchming, B.; Vallage, B.; Black, S.N.; Dann, J.H.; Kim, H.Y.; Konstantinidis, N.; Litke, A.M.; McNeil, M.A.; Taylor, G.; Booth, C.N.; Cartwright, S.; Combley, F.; Hodgson, P.N.; Kelly, M.S.; Lehto, M.; Thompson, L.F.; Affholderbach, K.; Boehrer, Armin; Brandt, S.; Grupen, C.; Hess, J.; Misiejuk, A.; Prange, G.; Sieler, U.; Giannini, G.; Gobbo, B.; Putz, J.; Rothberg, J.; Wasserbaech, S.; Williams, R.W.; Armstrong, S.R.; Elmer, P.; Ferguson, D.P.S.; Gao, Y.; Gonzalez, S.; Hayes, O.J.; Hu, H.; Jin, S.; McNamara, P.A., III; Nielsen, J.; Orejudos, W.; Pan, Y.B.; Saadi, Y.; Scott, I.J.; Walsh, J.; Wu, Sau Lan; Wu, X.; Zobernig, G.

    1999-01-01

    Radiative returns to the Z resonance (Z\\gamma events) are used to determine the LEP2 centre-of-mass energy from the data collected with the ALEPH detector in 1997. The average centre-of-mass energy is measured to be: E_CM = 182.50 +- 0.19 (stat.) +- 0.08 (syst.) GeV in good agreement with the precise determination by the LEP energy working group of 182.652 +- 0.050 GeV. If applied to the measurement of the W mass, its precision translates into a systematic error on M_W which is smaller than the statistical error achieved from the corresponding dataset.

  15. Single-acquisition method for simultaneous determination of extrinsic gamma-camera sensitivity and spatial resolution

    Energy Technology Data Exchange (ETDEWEB)

    Santos, J.A.M. [Servico de Fisica Medica, Instituto Portugues de Oncologia Francisco Gentil do Porto, E.P.E., Rua Dr. Antonio Bernardino de Almeida, 4200-072 Porto (Portugal)], E-mail: a.miranda@portugalmail.pt; Sarmento, S. [Servico de Fisica Medica, Instituto Portugues de Oncologia Francisco Gentil do Porto, E.P.E., Rua Dr. Antonio Bernardino de Almeida, 4200-072 Porto (Portugal); Alves, P.; Torres, M.C. [Departamento de Fisica da Universidade do Porto, Rua do Campo Alegre 687, 4169-007 Porto (Portugal); Bastos, A.L. [Servico de Medicina Nuclear, Instituto Portugues de Oncologia Francisco Gentil do Porto, E.P.E., Rua Dr. Antonio Bernardino de Almeida, 4200-072 Porto (Portugal); Ponte, F. [Servico de Fisica Medica, Instituto Portugues de Oncologia Francisco Gentil do Porto, E.P.E., Rua Dr. Antonio Bernardino de Almeida, 4200-072 Porto (Portugal)

    2008-01-15

    A new method for measuring simultaneously both the extrinsic sensitivity and spatial resolution of a gamma-camera in a single planar acquisition was implemented. A dual-purpose phantom (SR phantom; sensitivity/resolution) was developed, tested and the results compared with other conventional methods used for separate determination of these two important image quality parameters. The SR phantom yielded reproducible and accurate results, allowing an immediate visual inspection of the spatial resolution as well as the quantitative determination of the contrast for six different spatial frequencies. It also proved to be useful in the estimation of the modulation transfer function (MTF) of the image formation collimator/detector system at six different frequencies and can be used to estimate the spatial resolution as function of the direction relative to the digital matrix of the detector.

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

    International Nuclear Information System (INIS)

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

    2007-01-01

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

  17. Precise position of the Basal Choteč event and evolution of sedimentary environments near the Lower–Middle Devonian boundary: The magnetic susceptibility, gamma-ray spectrometric, lithological, and geochemical record of the Prague Synform (Czech Republic)

    Czech Academy of Sciences Publication Activity Database

    Koptíková, Leona

    2011-01-01

    Roč. 304, 1/2 (2011), s. 96-112 ISSN 0031-0182 R&D Projects: GA AV ČR KJB307020602; GA AV ČR IAAX00130702 Institutional research plan: CEZ:AV0Z30130516 Keywords : magnetic susceptibility * Gamma-ray spectrometry * Prague Synform * Lower–Middle Devonian Subject RIV: DB - Geology ; Mineralogy Impact factor: 2.392, year: 2011

  18. Comparison of three gamma ray isotopic determination codes: FRAM, MGA, and TRIFID

    International Nuclear Information System (INIS)

    Cremers, T.L.; Malcom, J.E.; Bonner, C.A.

    1994-01-01

    The determination of the isotopic distribution of plutonium and the americium concentration is required for the assay of nuclear material by calorimetry or neutron coincidence counting. The isotopic information is used in calorimetric assay to compute the effective specific power from the measured isotopic fractions and the known specific power of each isotope. The effective specific power is combined with the heat measurement to obtain the mass of plutonium in the assayed nuclear material. The response of neutron coincidence counters is determined by the 240 Pu isotopic fraction with contributions from the other even plutonium isotopes. The effect of the 240 Pu isotopic fraction and the other neutron contributing isotopes are combined as 240 Pu effective. This is used to calculate the mass of nuclear material from the neutron counting data in a manner analogous to the effective specific power in calorimeter. Comparisons of the precision and accuracy of calorimetric assay and neutron coincidence counting often focus only on the precision and accuracy of the heat measurement (calorimetry) compared to the precision and accuracy of the neutron coincidence counting statistics. The major source of uncertainty for both calorimetric assay and neutron coincidence counting often lies in the determination of the plutonium isotopic distribution ad determined by gamma ray spectroscopy. Thus, the selection of the appropriate isotopic distribution code is of paramount importance to good calorimetric assay and neutron coincidence counting. Three gamma ray isotopic distribution codes, FRAM, MGA, and TRIFID have been compared at the Los Alamos Plutonium Facility under carefully controlled conditions of similar count rates, count times, and 240 Pu isotopic fraction

  19. Application of Gamma and X-ray Technique (GXW) for Uranium and Plutonium Measurement

    International Nuclear Information System (INIS)

    Basuki Wibowo; Indro Yuwono

    2004-01-01

    The GXW method represents a generalization of the standard isotope measurement by special high resolution detector in that it exploits the full spectroscopic information contained in gamma spectrum from sample to achieve also a determination of sample mass fraction in the assay material. The method makes use of several gamma spectrometric analysis techniques as enrichment type measurements (IAMF), passive differential gamma absorptiometry (PDGA) and passive x-ray fluorescence analysis (PXRF), either individually or in combination, for determination of the element mass fraction from a single gamma spectrum. The approach works in principle for any kind sample, liquid and solid, provided the recommended geometry set up. A calibration or normalization with at least one reference sample is normally required for the mass fraction measurement. The measured sample mass fraction together with the knowledge of the net sample weight obtained from a weighing yield the total amount of sample. (author)

  20. Application of neutron-gamma analysis for determination of C/N ratio in compost

    Science.gov (United States)

    Neutron-gamma analysis is based on the acquisition of gamma rays from neutron irradiated study objects. The intensity and energy of the registered gamma rays gives information on the types and amounts of elements in the studied object. The use of this method for measurements of soil carbon demonstra...

  1. Quantitative determination of α-ionone, β-ionone, and β-damascenone and enantiodifferentiation of α-ionone in wine for authenticity control using multidimensional gas chromatography with tandem mass spectrometric detection.

    Science.gov (United States)

    Langen, Johannes; Wegmann-Herr, Pascal; Schmarr, Hans-Georg

    2016-09-01

    Native concentrations of α-ionone, β-ionone, and β-damascenone were studied in various authentic and commercial wines. In addition, the enantiomeric distribution of α-ionone was determined and its merits as a potential marker for aroma adulteration in wine were discussed. For extraction of volatiles, headspace solid-phase microextraction (HS-SPME) was applied, followed by heart-cut multidimensional gas chromatography coupled to tandem mass spectrometric detection for trace-level analysis. The enantioselective analysis of α-ionone was achieved with octakis(2,3-di-O-pentyl-6-O-methyl)-γ-cyclodextrin as the chiral selector in the separation column for gas chromatography (GC). In all the authentic wines studied, α-ionone showed a high enantiomeric ratio in favor of the (R)-enantiomer. Since an illegal addition of α-ionone in a racemic form changes the enantiomeric ratio, this ratio may serve as an adulteration marker. Concentrations varied between authenticity markers in wine.

  2. Extraction and preconcentration of trace Al and Cr from vegetable samples by vortex-assisted ionic liquid-based dispersive liquid-liquid microextraction prior to atomic absorption spectrometric determination.

    Science.gov (United States)

    Altunay, Nail; Yıldırım, Emre; Gürkan, Ramazan

    2018-04-15

    In the study, a simple, and efficient microextraction approach, which is termed as vortex-assisted ionic liquid-based dispersive liquid-liquid microextraction (VA-IL-DLLME), was developed for flame atomic absorption spectrometric analysis of aluminum (Al) and chromium (Cr) in vegetables. The method is based on the formation of anionic chelate complexes of Al(III) and Cr(VI) with o-hydroxy azo dye, at pH 6.5, and then extraction of the hydrophobic ternary complexes formed in presence of cetyltrimethylammonium bromide (CTAB) into a 125 μL volume of 1-butyl-3-methylimidazolium bis(trifluorosulfonyl)imide [C 4 mim][Tf 2 N]) as extraction solvent. Under optimum conditions, the detection limits were 0.02 µg L -1 in linear working range of 0.07-100 µg L -1 for Al(III), and 0.05 µg L -1 in linear working range of 0.2-80 µg L -1 for Cr(VI). After the validation by analysis of a certified reference material (CRM), the method was successfully applied to the determination of Al and Cr in vegetables using standard addition method. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Determination quercetin content, antioxidant and antimicrobial activity of genotype mutant Samosir shallots irradiated by gamma rays

    Science.gov (United States)

    Sinuraya, M.; Hanafiah, D. S.; Romulo, A.; Barus, A.

    2018-02-01

    The aim of the research was to study the variation in antioxidant and antimicrobial activity as well as the total quercetin content of the fifth generation genotypes mutant Samosir shallot irradiated by gamma rays. The studies conducted included the assessment of quercetin content, antioxidant and antimicrobial activity in shallot bulbs after long-term storage (6 months in the room temperature). Quercetin content of 20 selected genotype mutants of irradiated shallot bulbs along with untreated populations were calculated using quercetin (QU) as a standard. Antioxidant activities of 8 genotype mutant were determined using DPPH. Antimicrobial activity of bulb extracts were tested against six bacteria including Staphylococcus aurous, Enterococcus faecalis, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae and oneyeastCandida albicans. The results showed that population of genotype mutants irradiated with dosage 2Gy, 4 Gy, 5 Gy and 6 Gy have higher quercetin content than control samples. None of the genotype mutants exhibited antibacterial inhibitory against all microorganism tested except for the sample number 2 and 6 (bulbs generated from the plants irradiated by gamma rays with dosage at 2 Gy and 6 Gy). There was also none of the genotypes observed exhibited significant antioxidant efficacy.

  4. Determination of Pu isotopic composition and 241Am by high resolution gamma spectrometry on solid samples

    International Nuclear Information System (INIS)

    Sarkar, Arnab; Paul, Sumana; Aggarwal, Suresh K.; Tomar, Bhupendra S.

    2011-08-01

    The present report gives a detailed account of the development of non-destructive assay technique using high resolution gamma-ray spectrometry (HRGS) for determination of plutonium (Pu) isotopic composition and the 241 Am content in solid Pu samples. Energy range 120-420 keV was used in this study. The methodology involves in situ relative efficiency calibration during the measurement process itself, to reduce the errors and increase the reliability of the method. Twenty solid Pu samples of power reactor and research reactor grade were analyzed by this method and the results were compared with those obtained by thermal ionization mass spectrometry. The accuracy of the final results depends strongly upon the accuracy of the available nuclear data (decay constant, gamma abundance etc.). MATLAB based programme was written to perform the analysis. A counting time of 4 hour was chosen for achieving good statistics on the results for samples having 100-200 mg of Pu. The attainable accuracy is found to be 0.5-1% for the fissile isotopes ( 239 Pu + 241 Pu) and 5-10% for 241 Am content. (author)

  5. Radioimmunological determination of alphafetoprotein and gamma camera scintigraphy in patients with tumours of the testes

    International Nuclear Information System (INIS)

    Milkov, V.; Sultanov, S.

    1989-01-01

    By means of radioimmunological method the blood serum concentrations of alphafetoprotein (AFP) were investigated in 35 patients with histologically confirmed tumours of the testes prior to surgical intervention. Parallely in all patients gamma camera scintigraphy of the testes was performed. Seven of all investigated 15 patients with seminoma of the testes had increased concentrations of AFP in the blood serum. In 7 of the examinated 10 patients with diagnosis teratoma of the testes increased blood serum concentrations of AFP were established, while 6 of the examined patients with embryonic tumour of the testis had increased blood serum concentrations of AFP. In comparison with the results established in the control group of 30 healthy males, this increase of AFP was statistically reliable. All examined patients showed positive scintigraphic findings, which confirmed the diagnosis of tumour of the testes. It is concluded that the parallel determination of blood serum AFP and gamma camera investigation of the testes could be successfully apllied in the diagnosis of these malignant diseases

  6. Determination of Beryllium-7 in Water Hyacinth Using Gamma-Ray Spectrometry

    International Nuclear Information System (INIS)

    Yimchalam, Nopporn; Chankow, Nares; Yangchauy, Udon

    2009-07-01

    Full text: Beryllium-7 (7 B e) is a cosmogenic radionuclide produced in the upper atmosphere and enters the lower atmosphere by atmospheric circulation processes. About 90% of 7 B e decays directly through electron capture to 7 L i at ground state and about 10% to 7 L i at 1 s t excited state followed by 477.6 keV gamma-ray emission with a half-life of 53.3 days. The aim of this research was to measure 7 B e activity in environmental samples including water and aquatic plants. From the preliminary investigation by measurement of the 477.6 keV gamma-ray peak, 7 B e could be found in fresh Water Hyacinth samples. Thus, Water Hyacinth samples were then collected at different times of the year 2007 - 2008 in an area of Bang Khaen campus of Kasetsart University for determination of 7 B e activity using a HPGe detector. It was found that 7 B e specific activity was about 4-7 Bq/kg in the samples collected in rainy season during August-October 2007 and in June 2008 but could not detect in dry seasons i.e. summer and winter. The specific activity of 7 B e in Water Hyacinth sample depended on rainfalls as expected

  7. Log-Determinant Divergences Revisited: Alpha-Beta and Gamma Log-Det Divergences

    Directory of Open Access Journals (Sweden)

    Andrzej Cichocki

    2015-05-01

    Full Text Available This work reviews and extends a family of log-determinant (log-det divergences for symmetric positive definite (SPD matrices and discusses their fundamental properties. We show how to use parameterized Alpha-Beta (AB and Gamma log-det divergences to generate many well-known divergences; in particular, we consider the Stein’s loss, the S-divergence, also called Jensen-Bregman LogDet (JBLD divergence, Logdet Zero (Bhattacharyya divergence, Affine Invariant Riemannian Metric (AIRM, and other divergences. Moreover, we establish links and correspondences between log-det divergences and visualise them on an alpha-beta plane for various sets of parameters. We use this unifying framework to interpret and extend existing similarity measures for semidefinite covariance matrices in finite-dimensional Reproducing Kernel Hilbert Spaces (RKHS. This paper also shows how the Alpha-Beta family of log-det divergences relates to the divergences of multivariate and multilinear normal distributions. Closed form formulas are derived for Gamma divergences of two multivariate Gaussian densities; the special cases of the Kullback-Leibler, Bhattacharyya, Rényi, and Cauchy-Schwartz divergences are discussed. Symmetrized versions of log-det divergences are also considered and briefly reviewed. Finally, a class of divergences is extended to multiway divergences for separable covariance (or precision matrices.

  8. Field preconcentration of cadmium from seawater by using a minicolumn packed with Amberlite XAD-4/4-(2-pyridylazo) resorcinol and its flow-injection-flame atomic absorption spectrometric determination at the ng L{sup -1} Level

    Energy Technology Data Exchange (ETDEWEB)

    Yebra, M.C.; Salgado, J.; Puig, L.; Moreno-Cid, A. [Department of Analytical Chemistry, Nutrition and Bromatology, Faculty of Chemistry, University of Santiago de Compostela, 15782-Santiago de Compostela (Spain)

    2002-10-01

    A flow injection analysis-flame atomic absorption spectrometric method for the determination of cadmium in seawater was developed with the aim of yielding a sensitive assay with a low detection limit. The method employs a field flow preconcentration technique involving a minicolumn containing Amberlite XAD-4 impregnated with the complexing agent 4-(2-pyridylazo) resorcinol. A Plackett-Burman 2{sup 7} x 3/32 design for seven factors (sample pH, sample flow rate, eluent volume, eluent concentration, eluent flow rate, ethanol percentage in the eluent and minicolumn diameter) was carried out in order to find the significant variables affecting the field continuous preconcentration system (FCPS) and the flow injection elution manifold for cadmium determination in seawater samples by flame atomic absorption spectrometry. Cadmium can be preconcentrated with an enrichment factor of 1053 for a sample volume of 200 mL and a preconcentration time of 57 min. In these experimental conditions, the method provides a linear relationship between absorbance and cadmium concentration in the range from 22-1900 ng L{sup -1}, with a detection limit (3SD) of 6 ng L{sup -1}. The precision (expressed as relative standard deviation) for eleven independent determinations reached values of 8.9-0.8% in cadmium solutions of 50-700 ng L{sup -1}. Analysis of certified reference materials (SLEW-3 and NASS-5) showed good agreement with the certified value. This procedure was applied to the determination of cadmium in seawater from Galicia (Spain). (orig.)

  9. 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)

  10. Improved gas chromatography-negative ion chemical ionization tandem mass spectrometric method for determination of 11-nor-Δ9-tetrahydrocannabinol-9-carboxylic acid in hair using mechanical pulverization and bead-assisted liquid-liquid extraction.

    Science.gov (United States)

    Kim, Jin Young; Cheong, Jae Chul; Lee, Jae Il; In, Moon Kyo

    2011-03-20

    A gas chromatography-negative ion chemical ionization tandem mass spectrometric (GC-NCI-MS/MS) method was developed and validated for the determination of 11-nor-Δ(9)-tetrahydrocannabinol-9-carboxylic acid (THC-COOH) in human hair. After decontamination, hair samples were weighed (25mg), mechanically pulverized with a bead mill, and incubated in 0.7 mL of 1.0M sodium hydroxide at 95 °C for 30 min. Bead-assisted liquid-liquid extraction was performed with n-hexane:ethyl acetate (9:1, v/v), a method developed in our laboratory. The extract was evaporated to dryness, derivatized with pentafluoropropanol and pentafluoropropionic anhydride, and analyzed by GC-MS/MS in the negative ion chemical ionization mode using methane as the reagent gas. The linear ranges were 0.05-10.0 pg/mg for THC-COOH with the coefficient of determination (r(2) = 0.9976). The intra-day and inter-day precisions were within 1.7 and 13.8%, respectively. The intra-day and inter-day accuracies were -4.8 to 10.0% and -3.9 to 3.8%, respectively. The limit of detection and quantification were 0.015 and 0.05 pg/mg, respectively. The recoveries were in the range of 79.4-87.1%. The results indicate that the proposed method is simple, rapid, accurate, and precise for determination of THC-COOH in hair. The method identified THC-COOH in hair specimens from suspected marijuana abusers. Copyright © 2011. Published by Elsevier Ireland Ltd.

  11. Improvement of passive shielding to reduce background components to determinate radioactivity at low energy gamma rays

    Energy Technology Data Exchange (ETDEWEB)

    Thanh, Tran Thien [VNUHCM-Univ. of Science, Ho Chi Minh City (Viet Nam). Dept. of Nuclear Engineering Physics; Ton Duc Thang Univ., Ho Chi Minh City (Viet Nam). Div. of Nuclear Physics; Loan, T.T.H.; Nhon, M.V.; Tao, C.V. [VNUHCM-Univ. of Science, Ho Chi Minh City (Viet Nam). Dept. of Nuclear Engineering Physics

    2014-06-15

    This paper describes a new system that has the ability to reduce background components to apply for environmental studies. This system uses gamma spectrometry with semi-empirical self-absorption correction and practical method for routine measurements of the mass activity radionuclides at low energy such as {sup 210}Pb (46.5 keV), {sup 234}Th (63.3 keV) and {sup 226}Ra (186.2 keV). The reliability and precision of proficiency test must pass for final scores all the analytical determinations of received ''acceptable'' for all radionuclides. Our work shows an experiment developed for the calculation of self-absorption correction in that case that the sample's chemical composition is unknown.

  12. Determination of scattered gamma radiation in the calibration of environmental dose rate meters

    DEFF Research Database (Denmark)

    Bøtter-Jensen, L.; Hedemann Jensen, P.

    1992-01-01

    Practical free-field and shadow-shield calibration techniques using a variety of environmental dose rate meters were studied, and experimental and theoretical determinations were made of the contribution of scattered photons to the air kerma rate from certificated Cs-137, Co-60 and Ra-226 gamma...... sources in different calibration geometries. Scattered air kerma rates from surrounding media were calculated with a Monte Carlo code and matched closely the experimental results. Calibration experiments comprised measurements in both open-field and garden environments to see how nearby buildings affected...... the detector responses. Insignificant differences of the order of 1 % between the results for the two geometries were found both experimentally and theoretically. It is thus concluded that the scattered radiation from surrounding buildings farther away than around 15 m from a calibration set-up contributes...

  13. High accuracy/high precision determination of 235U in nondestructive assay standards by gamma-ray spectroscopy

    International Nuclear Information System (INIS)

    Greenberg, R.R.; Carpenter, B.S.

    1984-01-01

    High precision gamma spectrometry measurements have been made on five sets of five uranium isotope abundance reference materials for nondestructive assay (NDA). These sets are intended for international safeguards use as primary reference materials for the determination of the 235 U abundance in homogeneous uranium bulk material by gamma spectrometry. The measurements are to determine the counting rate uniformity of the 235 U 185.7 keV gamma as well as the 235 U isotope abundance for each sample. Since the samples are packaged such that the U 3 O 8 is infinitely thick for the 185.7 keV gamma, the measured counting rate is not dependent on the material density. In addition, the activity observed by the detector is colimated to simulate calibration conditions used to measure bulk material in the field. The results of this study indicate that accuracy of 235 U determination via gamma spectrometry, in the range of few hundredths of a percent (2sigma), is achievable. The main requirement for achieving this level of accuracy is a set of standards whose 235 U isotope abundance are known to within 0.01% (2sigma)

  14. APPLICATION OF THE SPECTROMETRIC METHOD FOR CALCULATING THE DOSE RATE FOR CREATING CALIBRATION HIGHLY SENSITIVE INSTRUMENTS BASED ON SCINTILLATION DETECTION UNITS

    Directory of Open Access Journals (Sweden)

    R. V. Lukashevich

    2017-01-01

    Full Text Available Devices based on scintillation detector are highly sensitive to photon radiation and are widely used to measure the environment dose rate. Modernization of the measuring path to minimize the error in measuring the response of the detector to gamma radiation has already reached its technological ceiling and does not give the proper effect. More promising for this purpose are new methods of processing the obtained spectrometric information. The purpose of this work is the development of highly sensitive instruments based on scintillation detection units using a spectrometric method for calculating dose rate.In this paper we consider the spectrometric method of dosimetry of gamma radiation based on the transformation of the measured instrumental spectrum. Using predetermined or measured functions of the detector response to the action of gamma radiation of a given energy and flux density, a certain function of the energy G(E is determined. Using this function as the core of the integral transformation from the field to dose characteristic, it is possible to obtain the dose value directly from the current instrumentation spectrum. Applying the function G(E to the energy distribution of the fluence of photon radiation in the environment, the total dose rate can be determined without information on the distribution of radioisotopes in the environment.To determine G(E by Monte-Carlo method instrumental response function of the scintillator detector to monoenergetic photon radiation sources as well as other characteristics are calculated. Then the whole full-scale energy range is divided into energy ranges for which the function G(E is calculated using a linear interpolation.Spectrometric method for dose calculation using the function G(E, which allows the use of scintillation detection units for a wide range of dosimetry applications is considered in the article. As well as describes the method of calculating this function by using Monte-Carlo methods

  15. On-line preconcentration of cobalt in drinking water using a minicolumn packed with activated carbon coupled to electrothermal atomic absorption spectrometric determination

    Energy Technology Data Exchange (ETDEWEB)

    Cerutti, Soledad; Moyano, Susana; Gasquez, Jose A.; Stripeikis, Jorge; Olsina, Roberto A.; Martinez, Luis D. E-mail: ldm@unsl.edu.ar

    2003-11-21

    An on-line flow injection preconcentration-electrothermal atomic absorption spectrometry method is developed for trace determination of cobalt in drinking water samples by sorption on a conical minicolumn packed with activated carbon at pH 9.5. The cobalt was eluted from the minicolumn with 10% (v/v) nitric acid. An enrichment factor of 190-fold for a sample volume of 10 ml was obtained. The detection limit (DL) value for the preconcentration method proposed was 5 ng l{sup -1}. The precision for 10 replicate determinations at the 50 ng l{sup -1} Co level was 4.7% relative standard deviation. The calibration graph using the preconcentration system for cobalt was linear with a correlation coefficient of 0.9993 at levels near the DLs up to at least 0.35 {mu}g l{sup -1}. The method was successfully applied to the determination of cobalt in drinking water samples.

  16. [Butanol extraction combined with dilute hydrochloric acid dissolution-atomic fluorescence spectrometric method for indirect determination of molybdenum in Chinese herbal medicine].

    Science.gov (United States)

    Lu, Jian-Ping; Geng, Guo-Xing; Tang, Yan-Kui; Lu, Zhi-Yong

    2012-12-01

    A method for indirectly determining the molybdenum in Chinese herbal medicine by butanol extraction and dilute hydrochloric acid dissolution was established for atomic fluorescence spectrometry. The molybdoarsenate heteropoly acid, formed in the presence of As(V) and ammonium molybdate in 0.3 mol x L(-1) sulphuric acid medium, was separated and enriched in the organic solvent, then the evaporation of organic reagent was implemented and the left residue was dissolved in dilute hydrochloric acid in which the arsenic content was determined on behalf of molybdenum. In the optimum experimental conditions, molybdenum content in 0-15 microg x L(-1) range depicts a good linear relationship, the detection limit and relative standard deviation of 0.44 microg x L(-1) and 1.1% were obtained, respectively. Spiked Chinese herbal medicine samples were determined with the proposed method, and recoveries of 95.6%-101.3% were achieved.

  17. Preconcentration and atomic absorption spectrometric determination of cadmium, cobalt, copper, iron, lead, manganese, nickel and zinc in water samples using 6-methyl-2-pyridinecarboxaldehyde-4-phenyl-3-thiosemicarbazone

    International Nuclear Information System (INIS)

    Khuhawar, M.Y.; Das, P.; Dewani, V.K.

    2005-01-01

    The reagent 6-methyl-2-pyridinecarboxaldehyde-4-phenyl-3-thiosemicarbazone (MPAPT) has been examined for the pre-concentration of metal ions and determination using air acetylene flame atomic absorption spectrometer. The method is based on the complexation and extraction of cadmium (II), cobalt(III), copper(II), lead(II), nickel(II), iron(II), iron(II), manganese(II) and zinc(II) in chloroform. The metal iron are back extracted in nitric acid (1:1) or after evaporation of solvent the residue is digested in nitric acid. After necessary adjustment of volume the metal ions were determined in aqueous solution. Pre-concentration is obtained 10-25 times. Metal ions recovery was 95.4-100.8% with coefficient of variation 0.2-7.5%. The method used for the determination of metals in canal and sewerage waters, within 2-6433 mu g/L with C. V 0.-5.2%. (author)

  18. Calibration of a Gamma Spectrometry System Used for the Determination of Cs-137 in Spanish Soils

    International Nuclear Information System (INIS)

    Barreraa, M.; Romero, M. L.; Valino, F.

    2008-01-01

    The document describes the methodology used at CIEMAT in order to determine, by gamma spectrometry, the background levels of the radionuclide Cs-137 in soils of the Spanish peninsular territory. the work is a part of an extensive research project developed jointly by the University of the Basque Country (UPV-EHU) and the CIEMAT, endellite Content and migration of radiocaesium and radiostrontium in Spanish soils, which is funded by the Plan I+D of the Spanish Nuclear Security Council (CSN). The objective of the project is to establish the reference levels of man-made radionuclides in Spanish soils, with respect to which the evaluation of a possible posterior accidental release of radioactive material could be appraised. The activity concentration of the fission products Cs-137 has been determined in 34 soil cores extracted from representative Spanish soils type zones. This publication describes the experimental system employed, its calibration, the particular conditions applied to perform the measurements, as well as the experimental validation of the methodology. The activity profiles and inventories of the radioactive element so obtained are also presented. The estimation of the background Cs-137 reference levels, will provide a basis for later applications as the study of the spatial distribution in the region, the determination of the correlation between the deposited activity and the meteorological conditions, or the calculation of the specific migration parameters of the radioactive elements in Mediterranean conditions. (Author) 15 refs

  19. Determination of the anthraquinones aloe-emodin and aloin-A by liquid chromatography with mass spectrometric and diode array detection.

    Science.gov (United States)

    Elsohly, Mahmoud A; Gul, Waseem; Avula, Bharathi; Khan, Ikhlas A

    2007-01-01

    Methods using liquid chromatography/mass spectrometry (LC/MS) and LC with diode array detection (DAD) in the UV range (LC/UV) were developed for the determination of low levels of the anthraquinones aloe-emodin and aloin-A (barbaloin) in aloe-based products. The methods were used to analyze several commercial products (liquids, semisolids, and solids) for the 2 anthraquinones. The wavelengths used for quantification of aloin-A, aloe-emodin, and emodin (internal standard) by DAD were 357, 257, and 289 nm, respectively. The on-column sensitivities were 0.25 and 0.05 ng by LC/UV and 0.01 and 0.025 ng by LC/MS for aloin-A and aloe-emodin, respectively. The methods are simple and sensitive and provide reproducible results; therefore, they are suitable for the determination of these anthraquinones in various aloe-based products.

  20. Flame atomic absorption spectrometric determination of heavy metals in aqueous solution and surface water preceded by co-precipitation procedure with copper(II) 8-hydroxyquinoline

    Science.gov (United States)

    Ipeaiyeda, Ayodele Rotimi; Ayoade, Abisayo Ruth

    2017-12-01

    Co-precipitation procedure has widely been employed for preconcentration and separation of metal ions from the matrices of environmental samples. This is simply due to its simplicity, low consumption of separating solvent and short duration for analysis. Various organic ligands have been used for this purpose. However, there is dearth of information on the application of 8-hydroxyquinoline (8-HQ) as ligand and Cu(II) as carrier element. The use of Cu(II) is desirable because there is no contamination and background adsorption interference. Therefore, the objective of this study was to use 8-HQ in the presence of Cu(II) for coprecipitation of Cd(II), Co(II), Cr(III), Ni(II) and Pb(II) from standard solutions and surface water prior to their determinations by flame atomic absorption spectrometry (FAAS). The effects of pH, sample volume, amount of 8-HQ and Cu(II) and interfering ions on the recoveries of metal ions from standard solutions were monitored using FAAS. The water samples were treated with 8-HQ under the optimum experimental conditions and metal concentrations were determined by FAAS. The metal concentrations in water samples not treated with 8-HQ were also determined. The optimum recovery values for metal ions were higher than 85.0%. The concentrations (mg/L) of Co(II), Ni(II), Cr(III), and Pb(II) in water samples treated with 8-HQ were 0.014 ± 0.002, 0.03 ± 0.01, 0.04 ± 0.02 and 0.05 ± 0.02, respectively. These concentrations and those obtained without coprecipitation technique were significantly different. Coprecipitation procedure using 8-HQ as ligand and Cu(II) as carrier element enhanced the preconcentration and separation of metal ions from the matrix of water sample.

  1. Monoisotopic mass determination algorithm for selenocysteine-containing polypeptides from mass spectrometric data based on theoretical modeling of isotopic peak intensity ratios.

    Science.gov (United States)

    Kim, Jin Wook; Lee, Sunho; Park, Kunsoo; Na, Seungjin; Paek, Eunok; Park, Hyung Seo; Park, Heejin; Lee, Kong-Joo; Jeong, Jaeho; Kim, Hwa-Young

    2012-09-07

    Selenoproteins, containing selenocysteine (Sec, U) as the 21st amino acid in the genetic code, are well conserved from bacteria to human, except yeast and higher plants that miss the Sec insertion machinery. Determination of Sec association is important to find substrates and to understand redox action of selenoproteins. While mass spectrometry (MS) has become a common and powerful tool to determine an amino acid sequence of a protein, identification of a protein sequence containing Sec was not easy using MS because of the limited stability of Sec in selenoproteins. Se has six naturally occurring isotopes, ⁷⁴Se, ⁷⁶Se, ⁷⁷Se, ⁷⁸Se, ⁸⁰Se, and ⁸²Se, and ⁸⁰Se is the most abundant isotope. These characteristics provide a good indicator for selenopeptides but make it difficult to detect selenopeptides using software analysis tools developed for common peptides. Thus, previous reports verified MS scans of selenopeptides by manual inspection. None of the fully automated algorithms have taken into account the isotopes of Se, leading to the wrong interpretation for selenopeptides. In this paper, we present an algorithm to determine monoisotopic masses of selenocysteine-containing polypeptides. Our algorithm is based on a theoretical model for an isotopic distribution of a selenopeptide, which regards peak intensities in an isotopic distribution as the natural abundances of C, H, N, O, S, and Se. Our algorithm uses two kinds of isotopic peak intensity ratios: one for two adjacent peaks and another for two distant peaks. It is shown that our algorithm for selenopeptides performs accurately, which was demonstrated with two LC-MS/MS data sets. Using this algorithm, we have successfully identified the Sec-Cys and Sec-Sec cross-linking of glutaredoxin 1 (GRX1) from mass spectra obtained by UPLC-ESI-q-TOF instrument.

  2. [An ultrafast liquid chromatography-tandem mass spectrometric method for simultaneous determination of common artificial synthetic pigments in cooked meat products].

    Science.gov (United States)

    Chen, Xiaohong; Li, Xiaoping; Zhao, Yonggang; Pan, Shengdong; Jin, Micong

    2015-07-01

    A method based on ultrafast liquid chromatography-tandem mass spectrometry (UFLC-MS/MS) has been developed for the simultaneous determination of seven synthetic pigments in cooked meat product. After the cooked meat products were extracted by mixed extraction agent, purified by WAX column, the UFLC separation was performed on a Shim-pack XR-ODS II column (75 mm x 2.0 mm, 2.2 µm) with a linear gradient elution program of acetonitrile and ammonium acetate (AmAc, 5 mmol/L) as the mobile phase. Electrospray ionization was applied and operated in the negative ion mode. The limits of quantitation (LOQs) for the seven synthetic pigments were in the range of 0.7-5.0 µg/kg. The calibration curves showed good linearities for the seven analytes in their detection ranges, and the correlative coefficients (r) were more than 0.999. The recoveries were between 88.2%-106.5% with the RSDs in the range of 1.2%-5.0%. The method is sensitive, reproducible, quick and adapts to the simultaneous determination of the seven synthetic pigments in cooked meat product.

  3. Tween 80 coated alumina: An alternative support for solid phase extraction of copper, nickel, cobalt and cadmium prior to flame atomic absorption spectrometric determination

    Directory of Open Access Journals (Sweden)

    S.Z. Mohammadi

    2016-11-01

    Full Text Available The potential of coated alumina as a sorbent for the simultaneous separation and preconcentration of copper, nickel, cobalt and cadmium ions has been investigated. Copper, nickel, cobalt and cadmium were adsorbed quantitatively on coated alumina in the pH of 6. The main factors such as pH, amount sorbent, sample and eluent flow rate, type and volume of elution solution and interfering ions on the sorption of metal ions have been investigated in detail. Under the optimum experimental conditions, the detection limits (3Sb of this method for Cu(II, Ni(II, Co(II and Cd(II ions were 0.4, 1.0, 1.2 and 0.2 ng mL−1 in the original solution, respectively. Seven replicate determinations of a mixture of 5.0 μg of Cu(II, Ni(II, Co(II and 1.0 μg of Cd(II ions in the original solution gave a mean absorbance of 0.093, 0.071, 0.066 and 0.049 with relative standard deviations 1.9%, 2.3%, 2.6% and 2.1%, respectively. The method has been applied for the determination of trace amounts of Cu(II, Ni(II, Co(II and Cd(II ions in tobacco, brewed tea and water samples with satisfactory results.

  4. A liquid chromatography-atmospheric pressure photoionization tandem mass spectrometric (LC-APPI-MS/MS) method for the determination of triterpenoids in medicinal plant extracts.

    Science.gov (United States)

    Gobo, Luciana Assis; Viana, Carine; Lameira, Osmar Alves; de Carvalho, Leandro Machado

    2016-08-01

    An analytical method using liquid chromatography-atmospheric pressure photoionization tandem mass spectrometry with toluene as a dopant was developed for the determination of triterpenes in medicinal plant extracts. The 12 compounds determined have been shown to exhibit biological activity, such as gastroprotective, hepatoprotective, anti-inflammatory, antiviral and anti-tumor effects. The parameters of the atmospheric pressure photoionization interface were optimized to obtain the highest possible sensitivity for all of the compounds. The limits of detection and quantification ranged from 0.4 to 157.9 µg l -1 and 1.3 to 526.4 µg l -1 , respectively. The method was validated and applied to extracts of five medicinal plants species (Mansoa alliacea (Lam.) A.H.Gentry, Bauhinia variegata var variegata, Bauhinia variegata var alboflava, Cecropia obtuse Trécul and Cecropia palmate Willd) from the Amazonian region. The concentrations of the six triterpenes quantified in the samples ranged from 0.424 mg kg -1 for ursolic acid to 371.96 mg kg -1 for β-amyrin, which were quantified by using the standard addition method (n = 3). Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

  5. Determination of calcium, magnesium, sodium, and potassium in foodstuffs by using a microsampling flame atomic absorption spectrometric method after closed-vessel microwave digestion: method validation.

    Science.gov (United States)

    Chekri, Rachida; Noël, Laurent; Vastel, Christelle; Millour, Sandrine; Kadar, Ali; Guérin, Thierry

    2010-01-01

    This paper describes a validation process in compliance with the NFIEN ISO/IEC 17025 standard for the determination of the macrominerals calcium, magnesium, sodium, and potassium in foodstuffs by microsampling with flame atomic absorption spectrometry after closed-vessel microwave digestion. The French Standards Commission (Agence Francaise de Normalisation) standards NF V03-110, NF EN V03-115, and XP T-90-210 were used to evaluate this method. The method was validated in the context of an analysis of the 1322 food samples of the second French Total Diet Study (TDS). Several performance criteria (linearity, LOQ, specificity, trueness, precision under repeatability conditions, and intermediate precision reproducibility) were evaluated. Furthermore, the method was monitored by several internal quality controls. The LOQ values obtained (25, 5, 8.3, and 8.3 mg/kg for Ca, Mg, Na, and K, respectively) were in compliance with the needs of the TDS. The method provided accurate results as demonstrated by a repeatability CV (CVr) of < 7% and a reproducibility CV (CVR) of < 12% for all the elements. Therefore, the results indicated that this method could be used in the laboratory for the routine determination of these four elements in foodstuffs with acceptable analytical performance.

  6. Multiresidue analysis of pesticides in olive oil by gel permeation chromatography followed by gas chromatography-tandem mass-spectrometric determination

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez, Andres Garcia [Department of Physical and Analytical Chemistry, E.P.S. of Linares, University of Jaen, E-23700 Linares, Jaen (Spain); Martos, Natividad Ramos [Department of Physical and Analytical Chemistry, Faculty of Sciences, University of Jaen, E-23071 Jaen (Spain); Ballesteros, Evaristo [Department of Physical and Analytical Chemistry, E.P.S. of Linares, University of Jaen, E-23700 Linares, Jaen (Spain)]. E-mail: eballes@ujaen.es

    2006-02-03

    A method for the multiresidue analysis of olive oil samples for 26 pesticides is proposed. Residual pesticides are extracted from oil using an n-hexane/acetonitrile mixture, extracts being cleaned-up by gel permeation chromatography (GPC) for analysis by gas chromatography-tandem mass spectrometry (GC-MS/MS). Electron ionization and chemical ionization are employed in a single analysis for the determination of pesticides. Pesticide recoveries from virgin and refined olive oil spiked with 10, 100 and 250 {mu}g/kg concentrations of the pesticides ranged from 83.8 to 110.3%. The proposed method features good sensitivity: its limits of quantification are low enough to allow pesticide residues to be determined at concentrations below the maximum residue levels legally accepted. The precision, expressed as relative standard deviation, ranges from 4.93 to 8.11%. Applicability was tested on 40 olive oil samples. Several pesticides were detected in most of the virgin olive oil samples. By contrast, refined olive samples contained few pesticides, and only endosulfan sulphate was detected in all.

  7. Gastrointestinal behavior of orally administered radiolabeled erythromycin pellets in man as determined by gamma scintigraphy

    Energy Technology Data Exchange (ETDEWEB)

    Digenis, G.A.; Sandefer, E.P.; Parr, A.F.; Beihn, R.; McClain, C.; Scheinthal, B.M.; Ghebre-Sellassie, I.; Iyer, U.; Nesbitt, R.U.; Randinitis, E. (Univ. of Kentucky, Lexington (USA))

    1990-07-01

    The behavior of single 250-mg doses of a multiparticulate form of erythromycin base (ERYC(R)), each including five pellets radiolabeled with neutron-activated samarium-153, was observed by gamma scintigraphy in seven male subjects under fasting and nonfasting conditions. The residence time and locus of radiolabeled pellets within regions of the gastrointestinal tract were determined and were correlated with plasma concentrations of erythromycin at coincident time points. Administration of food 30 minutes postdosing reduced fasting plasma erythromycin Cmax and area under the plasma erythromycin versus time curve (AUC) values by 43% and 54%, respectively. Mean peak plasma concentration of erythromycin (Cmax) in the fasting state was 1.64 micrograms/mL versus 0.94 micrograms/mL in the nonfasting state. Total oral bioavailability, as determined by mean AUC (0-infinity) of the plasma erythromycin concentration versus time curve, was 7.6 hr/micrograms/mL in the fasted state, versus 3.5 hr/micrograms/mL in the nonfasting state. Mean time to peak plasma erythromycin concentration (tmax) in the fasting state was 3.3 hours, versus 2.3 hours in the nonfasting state. Plasma concentrations of erythromycin in both fasting and nonfasting states were within acceptable therapeutic ranges.

  8. Gastrointestinal behavior of orally administered radiolabeled erythromycin pellets in man as determined by gamma scintigraphy

    International Nuclear Information System (INIS)

    Digenis, G.A.; Sandefer, E.P.; Parr, A.F.; Beihn, R.; McClain, C.; Scheinthal, B.M.; Ghebre-Sellassie, I.; Iyer, U.; Nesbitt, R.U.; Randinitis, E.

    1990-01-01

    The behavior of single 250-mg doses of a multiparticulate form of erythromycin base (ERYC(R)), each including five pellets radiolabeled with neutron-activated samarium-153, was observed by gamma scintigraphy in seven male subjects under fasting and nonfasting conditions. The residence time and locus of radiolabeled pellets within regions of the gastrointestinal tract were determined and were correlated with plasma concentrations of erythromycin at coincident time points. Administration of food 30 minutes postdosing reduced fasting plasma erythromycin Cmax and area under the plasma erythromycin versus time curve (AUC) values by 43% and 54%, respectively. Mean peak plasma concentration of erythromycin (Cmax) in the fasting state was 1.64 micrograms/mL versus 0.94 micrograms/mL in the nonfasting state. Total oral bioavailability, as determined by mean AUC (0-infinity) of the plasma erythromycin concentration versus time curve, was 7.6 hr/micrograms/mL in the fasted state, versus 3.5 hr/micrograms/mL in the nonfasting state. Mean time to peak plasma erythromycin concentration (tmax) in the fasting state was 3.3 hours, versus 2.3 hours in the nonfasting state. Plasma concentrations of erythromycin in both fasting and nonfasting states were within acceptable therapeutic ranges

  9. Determination of primary bond scissions by mass spectrometric analysis of ultrasonic degradation products of poly(ethylene oxide-block-propylene oxide) copolymers.

    Science.gov (United States)

    Watanabe, Takehiro; Okabayashi, Masanori; Kurokawa, Daisuke; Nishimoto, Yukari; Ozawa, Tomoyuki; Kawasaki, Hideya; Arakawa, Ryuichi

    2010-07-01

    Ultrasonic degradation of poly(ethylene oxide-block-propylene oxide) copolymers consisting of a hydrophilic and a hydrophobic portion was studied with the aim to determine the location of bonds involved in the initial scission of the copolymers. LC-APCI-IT-MS and LC-APCI-orbitrap-MS were used for the detailed structural analysis of degradation products. The results indicated that initial bond scissions occurred principally at the boundary regions between backbones of polyethylene oxide (PEO) and polypropylene oxide (PPO) chains. Further structural analysis revealed the presence of oxygen adducts in the degradation products. Comparison with a thermal degradation carried out in helium atmosphere, one can conclude that the oxygen adducts are formed by radical reaction with water or dissolving oxygen molecules. The study demonstrated that chemical reactions as well as physical bond stress scissions are involved in the ultrasonic degradation of the copolymers. 2010 John Wiley & Sons, Ltd.

  10. Determination of evaporation coefficients of melt components of B2O3-GeO2 system by mass-spectrometric method

    International Nuclear Information System (INIS)

    Stolyarova, V.L.; Ambrok, A.G.; Nikolaev, E.N.; Semenov, G.A.

    1977-01-01

    Determined are the evaporation coefficients of the components of a glass-like system constituting boron oxide and germanium dioxide. Measurements were performed from the platinum channel and platinum effusion chamber of a low-temperature evaporator. Evaporation from the platinum channel was assumed to take place from an open surface in accord with Lengmuir, and that from the platinum chamber in accord with Knudsen. The evaporation coefficient was calculated on the basis of the Motzfeldt equation. In boron germanate glasses, the evaporation coefficient of germanium dioxide was shown to differ from the evaporation coefficient of pure germanium dioxide. Within the margin of error involved in the calculations, the evaporation coefficient of boron oxide coincides with the evaporation coefficient of pure boron oxide

  11. Novel solid phase extraction procedure for gold(III) on Dowex M 4195 prior to its flame atomic absorption spectrometric determination

    International Nuclear Information System (INIS)

    Tuzen, Mustafa; Saygi, Kadriye O.; Soylak, Mustafa

    2008-01-01

    A method for solid phase extraction (SPE) of gold(III) using Dowex M 4195 chelating resin has been developed. The optimum experimental conditions for the quantitative sorption of gold(III), pH, effect of flow rates, eluent types, sorption capacity and the effect of diverse ions on the sorption of gold(III) have been investigated. The chelating resin can be reused for more than 100 cycles of sorption-desorption without any significant change in sorption of gold(III) ions. The recovery values for gold(III) and detection limit (LOD) of gold were greater than 95% and 1.61 μg L -1 , respectively. The preconcentration factor was 31. The relative standard deviation of the method was -1 . The proposed method has been applied for the determination of gold(III) in some real samples including water, soil and sediment samples

  12. Diaion HP-2MG modified with 2-(2,6-dichlorobenzylideneamino) benzenethiol as new adsorbent for solid phase extraction and flame atomic absorption spectrometric determination of metal ions.

    Science.gov (United States)

    Ghaedi, M; Montazerozohori, M; Haghdoust, S; Zaare, F; Soylak, M

    2013-04-01

    A solid phase extraction method for enrichment-separation and the determination of cobalt (Co(2+)), copper (Cu(2+)), nickel (Ni(2+)), zinc (Zn(2+)) and lead (Pb(2+)) ions in real samples has been proposed. The influences of some analytical parameters like pH, flow rate, eluent type and interference of matrix ions on recoveries of analytes were optimized. The limits of detection were found in the range of 1.6-3.9 µg L(-1), while preconcentration factor for all understudy metal ions were found to be 166 with loading half time (t 1/2) less than 10 min. The procedure was applied for the enrichment-separation of analyte ions in environmental samples with recoveries higher than 94.8% and relative SD <4.9% (N = 5).

  13. Development of a portable mass spectrometric system for determination of isotopic composition of solid uranium samples using fluorine volatilization. Final report

    International Nuclear Information System (INIS)

    Loge, G.

    1994-01-01

    Using hardware and materials supplied by LANL, a prototype quadrupole mass spectrometer system designed for portable field analysis of isotopic composition of solid uranium samples was assembled and tested. The system contained the capability for fluorine volatilization of solid uranium samples with gas introduction, which was successfully tested and demonstrated using 100 mg samples of U 3 O 8 . Determination of precision and accuracy for measuring isotopic composition was performed using isotopic standards. Use with soil samples containing uranium were also attempted. Silicates in the soil forming SiF 4 were found to be a kinetic bottleneck to the formation of UF 6 . This could be avoided by performing some sort of chemical separation as a pre-treatment step, which was demonstrated using nitric acid

  14. Hydride generation atomic fluorescence spectrometric determination of As, Bi, Sb, Se(IV) and Te(IV) in aqua regia extracts from atmospheric particulate matter using multivariate optimization

    Energy Technology Data Exchange (ETDEWEB)

    Moscoso-Perez, Carmen [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain); Moreda-Pineiro, Jorge [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain)]. E-mail: jmoreda@udc.es; Lopez-Mahia, Purificacion [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain); Muniategui-Lorenzo, Soledad [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain); Fernandez-Fernandez, Esther [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain); Prada-Rodriguez, Dario [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira s/n, E-15071 A Coruna (Spain)

    2004-11-22

    A highly sensitive and simple method, based on hydride generation and atomic fluorescence detection, has been developed for the determination of As, Bi, Sb, Se(IV) and Te(IV) in aqua regia extracts from atmospheric particulate matter samples. Atmospheric particulates matter was collected on glass fiber filters using a medium volume sampler (PM1 particulate matter). Two-level factorial designs have been used to optimise the hydride generation atomic fluorescence spectrometry (HG-AFS) procedure. The effects of several parameters affecting the hydride generation efficiency (hydrochloric acid, sodium tetrahydroborate and potassium iodide concentrations and flow rates) have been evaluated using a Plackett-Burman experimental design. In addition, parameters affecting the hydride measurement (delay, analysis and memory times) have been also investigated. The significant parameters obtained (sodium tetrahydroborate concentration, sodium tetrahydroborate flow rate and analysis time for As; hydrochloric acid concentration and sodium tetrahydroborate flow rate for Se(IV); and sodium tetrahydroborate concentration and sodium tetrahydroborate flow rate for Te(IV)) have been optimized by using 2{sup n} + star central composite design. Hydrochloric acid concentration and sodium tetrahydroborate flow rate were the significant parameters obtained for Sb and Bi determination, respectively. Using a univariate approach these parameters were optimized. The accuracy of methods have been verified by using several certified reference materials: SRM 1648 (urban particulate matter) and SRM 1649a (urban dust). Detection limits in the range of 6 x 10{sup -3} to 0.2 ng m{sup -3} have been achieved. The developed methods were applied to several atmospheric particulate matter samples corresponding to A Coruna city (NW Spain)

  15. Development of new efficient method for isolation of phenolics from sea algae prior to their rapid resolution liquid chromatographic-tandem mass spectrometric determination.

    Science.gov (United States)

    Klejdus, Bořivoj; Plaza, Merichel; Šnóblová, Marie; Lojková, Lea

    2017-02-20

    The extraction of phenolic compounds from 4 different sea algae samples, three brown algae (Cystoseira abies-marina, C. abies-marina grinded under cryogenic conditions with liquid nitrogen, Undaria pinnatifida and Sargassum muticum) and one red algae (Chondrus crispus) via solid phase extraction using micro-elution solid-phase extraction (μ-SPE) plate method was studied. Prior to μ-SPE, 50mg of algae with 80% methanol mixture was extracted in hyphenated series by various extraction techniques, such as pressurized liquid extraction and Ika Ultra-Turrax ® Tube Drive, in combination with ultrasound assisted extraction. The μ-SPE plate technique reduced the time of sample pre-treatment thanks to higher sensitivity and pre-concentration effect. Selected groups of benzoic acid derivatives (p-hydroxybenzoic, protocatechuic, gallic, vanillic, and syringic acids), hydroxybenzaldehydes (4-hydroxybenzaldehyde, and 3,4-dihydroxybenzaldehyde), and cinnamic acid derivatives (p-coumaric, caffeic, ferulic, sinapic, and chlorogenic acids) were determined using rapid resolution liquid chromatography coupled to mass spectrometry detection with negative ion electrospray ionization (RRLC-ESI-MS) using multiple reactions monitoring. LOQs of measured samples varied in the range 0.23-1.68ng/mL and LODs in the range 0.07-0.52ng/mL. The applied method allowed a simultaneous determination of phenolics (i.e. free, esters soluble in methanol, glycosides, and esters insoluble in methanol) in less than 5min (including alkaline or acidic hydrolysis of raw extracts) from sea algae extracts. Copyright © 2016 Elsevier B.V. All rights reserved.

  16. Hydride generation atomic fluorescence spectrometric determination of As, Bi, Sb, Se(IV) and Te(IV) in aqua regia extracts from atmospheric particulate matter using multivariate optimization

    International Nuclear Information System (INIS)

    Moscoso-Perez, Carmen; Moreda-Pineiro, Jorge; Lopez-Mahia, Purificacion; Muniategui-Lorenzo, Soledad; Fernandez-Fernandez, Esther; Prada-Rodriguez, Dario

    2004-01-01

    A highly sensitive and simple method, based on hydride generation and atomic fluorescence detection, has been developed for the determination of As, Bi, Sb, Se(IV) and Te(IV) in aqua regia extracts from atmospheric particulate matter samples. Atmospheric particulates matter was collected on glass fiber filters using a medium volume sampler (PM1 particulate matter). Two-level factorial designs have been used to optimise the hydride generation atomic fluorescence spectrometry (HG-AFS) procedure. The effects of several parameters affecting the hydride generation efficiency (hydrochloric acid, sodium tetrahydroborate and potassium iodide concentrations and flow rates) have been evaluated using a Plackett-Burman experimental design. In addition, parameters affecting the hydride measurement (delay, analysis and memory times) have been also investigated. The significant parameters obtained (sodium tetrahydroborate concentration, sodium tetrahydroborate flow rate and analysis time for As; hydrochloric acid concentration and sodium tetrahydroborate flow rate for Se(IV); and sodium tetrahydroborate concentration and sodium tetrahydroborate flow rate for Te(IV)) have been optimized by using 2 n + star central composite design. Hydrochloric acid concentration and sodium tetrahydroborate flow rate were the significant parameters obtained for Sb and Bi determination, respectively. Using a univariate approach these parameters were optimized. The accuracy of methods have been verified by using several certified reference materials: SRM 1648 (urban particulate matter) and SRM 1649a (urban dust). Detection limits in the range of 6 x 10 -3 to 0.2 ng m -3 have been achieved. The developed methods were applied to several atmospheric particulate matter samples corresponding to A Coruna city (NW Spain)

  17. GAS-CHROMATOGRAPHIC DETERMINATION OF N-ACETYLISOPUTREANINE-GAMMA-LACTAM, A UNIQUE CATABOLITE OF N1-ACETYLSPERMIDINE

    NARCIS (Netherlands)

    HESSELS, J; KINGMA, AW; STURKENBOOM, MCJM; ELZINGA, H; VANDENBERG, GA; MUSKIET, FAJ

    1991-01-01

    A capillary gas chromatographic method with nitrogen-phosphorus detection for the determination of N-acetylisoputreanine-gamma-lactam (acisoga) in urine is described. The method was validated by comparing the results with those given by an isotope dilution mass fragmentographic method. Making use of

  18. Molecular determinants of desensitization and assembly of the chimeric GABA(A) receptor subunits (alpha1/gamma2) and (gamma2/alpha1) in combinations with beta2 and gamma2

    DEFF Research Database (Denmark)

    Elster, L; Kristiansen, U; Pickering, D S

    2001-01-01

    , as opposed to the staining of the (gamma2/alpha1)-containing receptors, which was only slightly higher than background. To explain this, the (alpha1/gamma2) and (gamma2/alpha1) chimeras may act like alpha1 and gamma2 subunits, respectively, indicating that the extracellular N-terminal segment is important...... in combination with beta2 or beta2gamma2. Surprisingly, the (alpha1/gamma2)(gamma2/alpha1)beta2 subunit combination did desensitize, indicating that the C-terminal segment of the alpha1 subunit may be important for desensitization. Moreover, desensitization was observed for the (alpha1/gamma2)beta2gamma2...

  19. Determination of difficult-to-measure Niobium-94 in nuclear wastes using extraction chromatography and gamma spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Temba, Eliane S.C.; Kastner, Geraldo F.; Reis Junior, Aluisio S.; Monteiro, Roberto P.G.; Moreira, Rubens M., E-mail: esct@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2015-07-01

    A radiochemical methodology for {sup 94}Nb determination in low-level radioactive wastes from nuclear power plant was proposed. Although it is a strong gamma emitter its concentration in radioactive waste samples are usually several orders of magnitude lower than that of other β-γ emitters, whose emissions affect the emission lines of {sup 94}Nb. The procedure involves extraction chromatography by using TEVA resin to isolate the Nb nuclide and the gamma spectrometry to its measurement. The chemical yield was around 75%. Samples of evaporator concentrate and spent resin were analyzed. (author)

  20. An Ultra-High Performance Liquid Chromatographic-Tandem Mass Spectrometric Method for the Determination of Sinomenine in Human Plasma after Transdermal Delivery of the Zhengqing Fengtongning Injection

    Directory of Open Access Journals (Sweden)

    Tingbo Chen

    2015-04-01

    Full Text Available A sensitive, precise and selective ultra-high performance liquid chromatography method coupled with triple-quadrupole mass spectrometry was developed and validated for the determination of trace amounts of sinomenine (ng/mL in minute volumes of human plasma. Fifty microliter plasma samples were precipitated using methanol to extract sinomenine. Separation was carried out on a C18 column with a water and acetonitrile mobile phase gradient with formic acid as an additive. The mass spectrometry data were obtained in the positive ion mode, and the transition of multiple reactions was monitored at m/z 330.2→181.0 for sinomenine quantification. The working assay range for sinomenine was linear from 0.1173 to 15.02 ng/mL with the lower limit of quantification of 0.1173 ng/mL. The precision and accuracy of the method was less than 15% in intra-day and inter-day experiments with a matrix effect of less than 6.5%. After validation, the quantitative method was applied to analyze sinomenine levels in human plasma after transdermal delivery of the Zhengqing Fengtongning Injection. The results showed that some samples contained sinomenine within the concentration range 0.4131–4.407 ng/mL.

  1. Development of on-line single-drop micro-extraction sequential injection system for electrothermal atomic absorption spectrometric determination of trace metals

    International Nuclear Information System (INIS)

    Anthemidis, Aristidis N.; Adam, Ibrahim S.I.

    2009-01-01

    A novel automatic sequential injection (SI) single-drop micro-extraction (SDME) system is proposed as versatile approach for on-line metal preconcentration and/or separation. Coupled to electrothermal atomic absorption spectrometry (ETAAS) the potentials of this SI scheme are demonstrated for trace cadmium determination in water samples. A non-charged complex of cadmium with ammonium diethyldithiophosphate (DDPA) was produced and extracted on-line into a 60 μL micro-drop of di-isobutyl ketone (DIBK). The extraction procedure was performed into a newly designed flow-through extraction cell coupled on a sequential injection manifold. As the complex Cd(II)-DDPA flowed continuously around the micro-droplet, the analyte was extracting into the solvent micro-drop. All the critical parameters were optimized and offered good performance characteristics and high preconcentration ratios. For 600 s micro-extraction time, the enhancement factor was 10 and the sampling frequency was 6 h -1 . The detection limit was 0.01 μg L -1 and the precision (RSD at 0.1 μg L -1 of cadmium) was 3.9%. The proposed method was evaluated by analyzing certified reference material

  2. Validation of a liquid chromatography-electrospray ionization tandem mass spectrometric method to determine six polyether ionophores in raw, UHT, pasteurized and powdered milk.

    Science.gov (United States)

    Pereira, Mararlene Ulberg; Spisso, Bernardete Ferraz; Jacob, Silvana do Couto; Monteiro, Mychelle Alves; Ferreira, Rosana Gomes; Carlos, Betânia de Souza; da Nóbrega, Armi Wanderley

    2016-04-01

    This study aimed to validate a method developed for the determination of six antibiotics from the polyether ionophore class (lasalocid, maduramicin, monensin, narasin, salinomycin and semduramicin) at residue levels in raw, UHT, pasteurized and powdered milk using QuEChERS extraction and high performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS). The validation was conducted under an in-house laboratory protocol that is primarily based on 2002/657/EC Decision, but takes in account the variability of matrix sources. Overall recoveries between 93% and 113% with relative standard deviations up to 16% were obtained under intermediate precision conditions. CCα calculated values did not exceed 20% the Maximum Residue Limit for monensin and 25% the Maximum Levels for all other substances. The method showed to be simple, fast and suitable for verifying the compliance of raw and processed milk samples regarding the limits recommended by Codex Alimentarius and those adopted in European Community for polyether ionophores. Copyright © 2015 Elsevier Ltd. All rights reserved.

  3. Novel solid phase extraction procedure for gold(III) on Dowex M 4195 prior to its flame atomic absorption spectrometric determination

    Energy Technology Data Exchange (ETDEWEB)

    Tuzen, Mustafa [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey)], E-mail: mtuzen@gop.edu.tr; Saygi, Kadriye O. [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey); Soylak, Mustafa [Erciyes University, Faculty of Science and Arts, Chemistry Department, 38039 Kayseri (Turkey)

    2008-08-15

    A method for solid phase extraction (SPE) of gold(III) using Dowex M 4195 chelating resin has been developed. The optimum experimental conditions for the quantitative sorption of gold(III), pH, effect of flow rates, eluent types, sorption capacity and the effect of diverse ions on the sorption of gold(III) have been investigated. The chelating resin can be reused for more than 100 cycles of sorption-desorption without any significant change in sorption of gold(III) ions. The recovery values for gold(III) and detection limit (LOD) of gold were greater than 95% and 1.61 {mu}g L{sup -1}, respectively. The preconcentration factor was 31. The relative standard deviation of the method was <5%. The adsorption capacity of the resin was 8.1 mg g{sup -1}. The proposed method has been applied for the determination of gold(III) in some real samples including water, soil and sediment samples.

  4. Quantitative determination of organochlorine pesticides in sewage sludges using soxtec, soxhlet and pressurized liquid extractions and ion trap mass-mass spectrometric detection.

    Science.gov (United States)

    Helaleh, M I H; Al-Omair, A; Ahmed, N; Gevao, B

    2005-06-01

    A new analytical method is described for the determination of organochlorine pesticides (OCPs) in sewage sludges using GC-ion trap-MS-MS. In this work, 16 organo-chlorine pesticides (OCPs) listed by the US Environmental Protection Agency (US EPA) as priority pollutants were separated and quantified. Sludge samples from three of Kuwait's wastewater treatment plants (WWTPs) were analyzed for organochlorine pesticides (OCPs). Spiked sludge samples were extracted with a mixture of (1:1 v/v) dichloromethane (DCM)/hexane. The extracts were cleaned on a silica/aluminum oxide column, then transferred to a gel permeation chromatography (GPC) column, before undergoing further silica/aluminum oxide clean-up; the presence of OCPs was then confirmed by GC-ion trap-MS-MS. Three extraction techniques, soxtec, soxhlet, and pressurized liquid extractions were utilized, compared and validated using the spiked sludge samples. The methods were validated in term of accuracy (recovery) and precision (RSD). The method recovery values varied from 76.1 to 92.9% for the three extraction techniques.

  5. Cloud point extraction and flame atomic absorption spectrometric determination of cadmium(II), lead(II), palladium(II) and silver(I) in environmental samples

    International Nuclear Information System (INIS)

    Ghaedi, Mehrorang; Shokrollahi, Ardeshir; Niknam, Khodabakhsh; Niknam, Ebrahim; Najibi, Asma; Soylak, Mustafa

    2009-01-01

    The phase-separation phenomenon of non-ionic surfactants occurring in aqueous solution was used for the extraction of cadmium(II), lead(II), palladium(II) and silver(I). The analytical procedure involved the formation of understudy metals complex with bis((1H-benzo [d] imidazol-2yl)ethyl) sulfane (BIES), and quantitatively extracted to the phase rich in octylphenoxypolyethoxyethanol (Triton X-114) after centrifugation. Methanol acidified with 1 mol L -1 HNO 3 was added to the surfactant-rich phase prior to its analysis by flame atomic absorption spectrometry (FAAS). The concentration of BIES, pH and amount of surfactant (Triton X-114) was optimized. At optimum conditions, the detection limits of (3 sdb/m) of 1.4, 2.8, 1.6 and 1.4 ng mL -1 for Cd 2+ , Pb 2+ , Pd 2+ and Ag + along with preconcentration factors of 30 and enrichment factors of 48, 39, 32 and 42 for Cd 2+ , Pb 2+ , Pd 2+ and Ag + , respectively, were obtained. The proposed cloud point extraction has been successfully applied for the determination of metal ions in real samples with complicated matrix such as radiology waste, vegetable, blood and urine samples.

  6. Rapid determination of acid herbicides in soil by liquid chromatography with tandem mass spectrometric detection based on dispersive solid phase extraction.

    Science.gov (United States)

    Kaczyński, Piotr; Łozowicka, Bożena; Jankowska, Magdalena; Hrynko, Izabela

    2016-05-15

    This study determined twenty six the highly sensitive phenoxy, pyridines, aliphatic and aromatic acid compounds in soil with a liquid chromatography tandem mass spectrometry. The samples were prepared by modified quick, easy, cheap, effective, rugged and safe (QuEChERS) analytical procedure in solid samples. Herbicides extraction effectiveness was evaluated at three different spiking levels (0.01, 0.1 and 1.0 mg kg(-1)). Fourteen different dispersive solid-phase extraction (d-SPE) sorbents in clean-up step were tested. The QuEChERS protocol with acidic alumina provided the highest number of pesticides with recoveries in the 70-120% range. The soil matrix effect was evaluated and for the majority of compounds were not significant, showing suppression or enhancement (±81-123%). The precision calculated as relative standard deviation (RSD) was below 22%. The linear relation was observed in the range 0.01-2.0 mg kg(-1) and the correlation coefficient R>0.999. The expanded measurement uncertainty was estimated as being on average, and was between 9% and 33%. The validated method was employed in the analysis of 309 real soil samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  7. Application of the gamma rays backscattering for determining the quantity of steel

    International Nuclear Information System (INIS)

    Huapaya P, B.F.

    1996-01-01

    This work tries to purpose a methodology based on the nuclear technology available in the country, for measuring the position and diameter of the reinforcing rods placed in reinforced concrete structures. The technique of gamma backscattering that utilizes the changes of density was used for determining the presence of steel (average density of concrete 2,5 g/cm 3 and steel 7,8 g/cm 3 ). The concrete test tubes of different resistances were prepared with diverse concentrations into the aggregates as crushed rock and coarse sand, and also with three steel rods of 0,5 inch separated by 4 inches among themselves. The source Cs-137 of 20 mCi in activity was a monoenergetic radioisotope of the element Cs from 662 KeV. The source was placed in a lead shield with a hole which generates a collimator beam of 2 mm. The detector was one type of scintillation (INa-Tl) 2 x 2 inch; it was sealed with lead and had a hole of 10 mm which worked as collimator. The shield was placed in an angle of 15 degrees over concrete surface in order to pick up the backscattering gamma rays by the concrete. The test tube was displaced over a little car affixed to a endless screw which permitted to reproduce displacements of 0,25 inch. The data recording was realized through a multichannel of 1024 channels where was accounted the number of counts viewed under the backscattering spectrum by the concrete. It is possible to determine the position and diameter of the steel rod into concrete, changing the parameters of detector collimator source, distance source-detector and type of concrete. Furthermore, it was shown that this same equipment can measure the density of the concrete. The applications of this equipment are used in the inspection works where it is necessary to make a non-destructive control of quality about the structure of building. (author). 7 refs., 46 tabs., 24 figs

  8. Mass spectrometric characterization of low-molecular-mass color pI markers and their use for direct determination of pI value of proteins.

    Science.gov (United States)

    Mazanec, Karel; Slais, Karel; Chmelík, Josef

    2006-12-01

    The use of low-molecular-mass color pI markers for the determination of pI values of proteins in gel isoelectric focusing (IEF) in combination with mass spectrometry is described. Different types of substituted phenols of known pI values within the mass range 250-400 were used here as pI markers. The pure, synthesized pI markers were studied by MALDI-TOF/TOF MS. Fragmentation studies of the pI markers were also performed. Only stable and well-characterized pI markers were used in this work. The selected pI markers were mixed with proteins, deposited on a gel and separated in a pH gradient. Color pI markers enable supervision of progress of the focusing process and also estimation of the position of the invisible focused bands. The separated bands of the pI markers (containing separated proteins) were excised, and the pI markers were eluted from each gel piece by water/ethanol and identified by MALDI-TOF/TOF MS. From the washed gel pieces the remaining carrier ampholytes were then washed out and proteins were in-gel digested with trypsin. The obtained peptides were measured by MALDI-TOF/TOF MS and the proteins identified via a protein database search. This procedure allows avoiding time-consuming protein staining and destaining procedures, which shortens the analysis time roughly by half. For comparison, IEF gels were stained with Coomassie Brilliant Blue R 250 and proteins in the gel bands were identified according to the standard proteomic protocol. This work has confirmed that our approach can give information about the correct pI values of particular proteins and shorten significantly the time of analysis.

  9. Chemometric analytical approach for the cloud point extraction and inductively coupled plasma mass spectrometric determination of zinc oxide nanoparticles in water samples.

    Science.gov (United States)

    Majedi, Seyed Mohammad; Lee, Hian Kee; Kelly, Barry C

    2012-08-07

    Cloud point extraction (CPE) with inductively coupled plasma mass spectrometry (ICPMS) was applied to the analysis of zinc oxide nanoparticles (ZnO NPs, mean diameter ~40 nm) in water and wastewater samples. Five CPE factors, surfactant (Triton X-114 (TX-114)) concentration, pH, ionic strength, incubation temperature, and incubation time, were investigated and optimized by orthogonal array design (OAD). A three-level OAD, OA(27) (3(13)) matrix was employed in which the effects of the factors and their contributions to the extraction efficiency were quantitatively assessed by the analysis of variance (ANOVA). Based on the analysis, the best extraction efficiency (87.3%) was obtained at 0.25% (w/v) of TX-114, pH = 10, salt content of 15 mM NaCl, incubation temperature of 45 °C, and incubation time of 30 min. The results showed that surfactant concentration, pH, incubation time, and ionic strength exert significant effects on the extraction efficiency. Preconcentration factors of 62 and 220 were obtained with 0.25 and 0.05% (w/v) TX-114, respectively. The relative recoveries of ZnO NPs from different environmental waters were in the range 64-123% at 0.5-100 μg/L spiked levels. The ZnO NPs extracted into the TX-114-rich phase were characterized by transmission electron microscopy (TEM) combined with energy-dispersive X-ray spectroscopy (EDS) and UV-visible spectrometry. Based on the results, no significant changes in size and shape of NPs were observed compared to those in the water before extraction. The extracted ZnO NPs were determined after microwave digestion by ICPMS. A detection limit of 0.05 μg/L was achieved for ZnO NPs. The optimized conditions were successfully applied to the analysis of ZnO NPs in water samples.

  10. Development and validation of a supercritical fluid chromatography method for the direct determination of enantiomeric purity of provitamin B5 in cosmetic formulations with mass spectrometric detection.

    Science.gov (United States)

    Khater, Syame; West, Caroline

    2015-01-01

    A rapid and efficient chiral supercritical fluid chromatography (SFC) method has been developed for the quantitative determination of panthenol enantiomers in cosmetic formulations (cream, lotion, wipe, and exfoliant). Indeed, the pharmacological effect only depends on the D form (Dexpanthenol) thus accurate measurement of its enantiomeric purity in formulated cosmetic products is of interest. The samples were prepared with liquid-liquid extraction followed by solid-phase extraction on Adsorbex amino cartridges. After testing several enantioselective columns in an attempt at reversing the elution order to have the minor enantiomer eluted first, the best separation of enantiomers and internal standard (N-acetyl-L-alanine) was achieved on a 3 μm-amylose-type immobilized polysaccharide chiral stationary phase (Chiralpak IA) in less than 6 min with a simple mobile phase comprising carbon dioxide and 11% methanol pumped at 2.3 mL/min, 25°C and 150 bar backpressure. Supercritical fluid chromatography coupled to both an optical diode-array detector and a user-friendly single-quadrupole mass spectrometer (Waters QDa) equipped with electrospray ionization source has been used. The on-line coupling ensures the technique to be more informative and improves detection sensitivity, as underivatized panthenol has a poor UV absorption. The limit of quantification (LOQ) achieved with single-ion recording was 0.5 μg/mL. The method was validated in terms of linearity, precision and accuracy and satisfactory results were obtained. Copyright © 2014 Elsevier B.V. All rights reserved.

  11. Method development for the concentration determination of a protein in human plasma utilizing 96-well solid-phase extraction and liquid chromatography/tandem mass spectrometric detection.

    Science.gov (United States)

    Ji, Qin C; Gage, Eric M; Rodila, Ramona; Chang, Min S; El-Shourbagy, Tawakol A

    2003-01-01

    Although liquid chromatography/tandem mass spectrometry (LC/MS/MS) technology has been widely used for quantitative analysis of small organic molecules, it has been a challenging task to quantitatively analyze protein samples utilizing this technology in biological matrices for pre-clinical and clinical studies. Here we present our initial results in method development for the quantitative determination of rK5 protein concentrations in human plasma samples utilizing LC/MS/MS technology. A protein similar in structure to rK5, but with a slightly reduced molecular weight, was used as internal standard. A 96-well solid-phase extraction procedure was developed to effectively extract protein analytes from plasma samples. Quantitative analysis was obtained by a novel approach of protein monitoring that employed selective reaction monitoring (SRM). Even though mass spectrometry of the internal standard protein gave no fragment ions, SRM monitoring greatly reduced background interference. Using samples prepared in human plasma with sodium EDTA as anticoagulant, a correlation coefficient (r(2)) of 0.9940 was obtained by producing a single standard curve with the injection of six rows of standards with a concentration range from 100 ng/mL to 10 microg/mL. The mean analytical recovery for these standards ranged from 91.5 to 103.6%. The CVs for individual standard levels ranged from 3.7 to 20.9%. The experiment was also repeated using samples prepared in human plasma with sodium heparin as anticoagulant, which produced a correlation coefficient (r(2)) of 0.9952 obtained from a single standard curve with the injection of four rows of standards with a concentration range from 50 ng/mL to 10 microg/mL. The mean analytical recovery for the standards ranged from 96.2 to 104.6%. The CVs for individual standard levels ranged from 2.6 to 15.6%. Copyright 2003 John Wiley & Sons, Ltd.

  12. On-line sequential injection dispersive liquid-liquid microextraction system for flame atomic absorption spectrometric determination of copper and lead in water samples.

    Science.gov (United States)

    Anthemidis, Aristidis N; Ioannou, Kallirroy-Ioanna G

    2009-06-30

    A simple, sensitive and powerful on-line sequential injection (SI) dispersive liquid-liquid microextraction (DLLME) system was developed as an alternative approach for on-line metal preconcentration and separation, using extraction solvent at microlitre volume. The potentials of this novel schema, coupled to flame atomic absorption spectrometry (FAAS), were demonstrated for trace copper and lead determination in water samples. The stream of methanol (disperser solvent) containing 2.0% (v/v) xylene (extraction solvent) and 0.3% (m/v) ammonium diethyldithiophosphate (chelating agent) was merged on-line with the stream of sample (aqueous phase), resulting a cloudy mixture, which was consisted of fine droplets of the extraction solvent dispersed entirely into the aqueous phase. By this continuous process, metal chelating complexes were formed and extracted into the fine droplets of the extraction solvent. The hydrophobic droplets of organic phase were retained into a microcolumn packed with PTFE-turnings. A portion of 300 microL isobutylmethylketone was used for quantitative elution of the analytes, which transported directly to the nebulizer of FAAS. All the critical parameters of the system such as type of extraction solvent, flow-rate of disperser and sample, extraction time as well as the chemical parameters were studied. Under the optimum conditions the enhancement factor for copper and lead was 560 and 265, respectively. For copper, the detection limit and the precision (R.S.D.) were 0.04 microg L(-1) and 2.1% at 2.0 microg L(-1) Cu(II), respectively, while for lead were 0.54 microg L(-1) and 1.9% at 30.0 microg L(-1) Pb(II), respectively. The developed method was evaluated by analyzing certified reference material and applied successfully to the analysis of environmental water samples.

  13. Quantitative determination of the enantiomers of methadone in human plasma and saliva by chiral column chromatography coupled with mass spectrometric detection.

    Science.gov (United States)

    George, Rani; Lobb, Michael; Haywood, Alison; Khan, Sohil; Hardy, Janet; Good, Phillip; Hennig, Stefanie; Norris, Ross

    2016-01-01

    Methadone is a potent lipophilic synthetic opioid that is effective in the treatment of cancer pain and perceived benefit in difficult pain control scenarios (especially in cases of neuropathic pain). The use of methadone in clinical practice is challenging however, due to the narrow therapeutic window and large inter- and intra-individual variability in therapeutic response. Quantitation of the enantiomers d- and l-methadone (d- and l-MTD) in plasma and saliva provides a basis for studying its pharmacokinetics in patients with cancer and for monitoring efficacy, toxicity and side-effects. This assay involves quantitation of the enantiomers of methadone using their respective deuterated internal standards, in plasma and saliva matrices with no impact of ion suppression in either matrix. The analytical recoveries of d- and l-MTD from the saliva collection devices (Salivette®) are optimised in this novel method with an accurate and simple extraction method employing dichloromethane. Optimal enantioselective separations were achieved using an α1-acid glycoprotein chiral stationary phase and triple quadrupole tandem mass spectrometer. Linearity was demonstrated over 0.05-1000µg/L for both enantiomers in plasma and in saliva with correlation coefficients greater than 0.998. The lower limit of quantitation (LLOQ) was determined to be 0.1µg/L in plasma and saliva for d- and l-MTD. Accuracy of the method ranges from 100% to 106% even at the LLOQ and total precision, expressed as the coefficient of variation, was between 0.2% and 4.4% for both analytes in both matrices. A simple one step extraction procedure resulted in recoveries greater than 95% for both analytes, at concentrations as low as 0.5µg/L, from the Salivette®. The validated method was applied successfully in 14 paired plasma and saliva samples obtained from adult patients with cancer pain receiving methadone. Copyright © 2015 Elsevier B.V. All rights reserved.

  14. Array-type sensor to determine corrosive conditions in high temperature water under gamma rays irradiation

    International Nuclear Information System (INIS)

    Satoh, T.; Tsukada, T.; Uchida, S.; Katoh, C.

    2010-01-01

    One of the problems to determine electrochemical corrosion potential (ECP) in high temperature water under irradiation is to apply long-lived and reliable reference electrodes. In order to avoid troubles due to the reference electrode, a new concept to determine ECP without the reference electrode has been proposed. Several metal plates are applied as working electrodes and at the same time as the reference electrodes. Potential of the metal plates with stable oxide films on their surfaces show stable values in high temperature water. As a result of the combination of their potential values, ECP of each metal can be determined without any specific reference electrode. Array-type sensors consisting of several metal plates, e.g., Fe, Ni, Cr, Zr, Pt, Pd, Re, Ir, with well developed oxide films on their surface were prepared for ECP measurement in high temperature water under neutron/gamma ray irradiations. In order to confirm the feasibility of this concept, responses of the redox potentials of the pure metals to changes in the simulated BWR reactor water conditions were measured and the ECP was determined by the differences in potentials between a couple of metal plates. Major conclusions of the study are as follows: 1) The redox potentials of the Fe, Pt, Zr, Ir, Pd, and Re electrodes showed the different dependences on the changes in O 2 and H 2 O 2 concentrations. The redox potentials of the electrodes increased as the oxidant concentrations increased except for Zr electrode. The potential of the Zr electrode was kept the very low potential at the wide range of O 2 and H 2 O 2 concentrations differed form the other electrodes. 2) It was estimated that the redox potential of highly soluble metal may be increased, while that of low soluble metal may be decreased by an oxide film. The stable oxide film would cause the stable potential response of the electrode with oxide film. 3) The relationship between the oxidant concentrations and the redox potentials of the

  15. A simple screening method for the determination of 230Th in soil and sediment samples by gamma-spectrometry

    International Nuclear Information System (INIS)

    Lozano, J.C.; Rodriguez, P.B.; Tome, F.V.

    2001-01-01

    A simple and easy to perform method for the determination of 230 Th in soil and sediment samples using gamma-spectrometry is proposed and compared with the more usual procedure using alpha-particle spectrometry. The proposed method involves an efficiency calibration for the specific determination of this radionuclide instead of a complete calibration of the spectra. A single density parameter is introduced to correct the efficiencies obtained from the reference sources. The activities of 230 Th determined by gamma-spectrometry and alpha-particle spectrometry are compared. The minimum detectable activity values obtained are completely adequate for 230 Th determination in soil and sediment samples, in which 230 Th activities are usually fairly high. Thus, this procedure is intended as a very easy way to obtain the activity of this radionuclide in these types of samples, at least as a screening method before carrying out other more laborious procedures. (author)

  16. High performance liquid chromatography determination of theobromine and caffeine in cocoa beans gamma irradiated

    Energy Technology Data Exchange (ETDEWEB)

    Soares, Anderson D.B. [Faculdade de Engenharia de Varginha, MG (Brazil); Mansur Neto, Elias [Minas Gerais Univ., Belo Horizonte, MG (Brazil)

    1997-12-01

    Irradiation is a processing technology that has been shown to be a wholesome process by many scientific studies conducted worldwide during the past 40 years, which has been approved by 37 countries. Irradiated foods have been studied so extensively, that the effects on foods are better understood than any other preservation process, including food freezing and dehydration. Cocoa beans has been commercially irradiated in countries such as Ivory Coast and Argentina. The alkaloids theobromine and caffeine are responsible for the mildly stimulating properties and bitter taste of cocoa and chocolate products. Previously fermented dried and nonfumigated cocoa beans were irradiated at doses of 0, 5.0, 10.0 and 20.0 kGy using Co-60 gamma rays. The samples were analysed for determining theobromine and caffeine contents in the cocoa beans by TIMBIE et al. (1978) high performance liquid chromatography (HPLC) method. Boiling water extracts were cooled, centrifuged and injected into the chromatograph. Theobromine and caffeine were quantitated at 273 nm and showed the tendency of decreasing as the dose of radiation increases. Theobromine and caffeine ranged from 42.3 to 37.1 mg/g and from 7.60 to 6.13 mg/g. respectively from 0 to 20.0 kGy. These results were discussed in relation to the possible acceptance of radiosterization of cocoa beans commercially up to the dose of 20.0 kGy. (author). 10 refs., 1 tab.

  17. Determination of gamma radiation lethal dose (LD50) and resveratrol cytotoxicity level in tumor cells line

    International Nuclear Information System (INIS)

    Magalhaes, Vanessa D.; Rogero, Sizue O.; Rogero, Jose R.; Cruz, Aurea S.

    2011-01-01

    Cancer is a disease with high incidence and it is considered a worldwide public health problem. Resveratrol is a polyphenol occurring naturally in a wide variety of plants according to response of ultraviolet radiation (UV) exposition or according to mechanical stress resulting of pathogens or chemical and physical agents. This polyphenol possesses a pharmacological activity of carcinogenesis inhibition in multiple levels. It also protects cells by scavenging the free radicals which are considered toxic products. These free radicals are formed of natural process of cell aging and also by incidence of ionizing radiation in the organism. Thus, resveratrol is considered as a cell radioprotector. On the other hand, in some elevated concentrations resveratrol may be considered as a radiosensitizing. The aim of this work was the determination of radiation lethal dose (LD 50 ) and also verifies the cytotoxicity level of resveratrol in tumor cells line: muco epidermoid pulmonary carcinoma cells (NCI-H292) and rhabdomyosarcoma cells (RD). The cytotoxicity test was performed by neutral red uptake assay. The results of resveratrol IC 50% in NCI-H292 cells was 192μM and in RD cells was 128μM; and RD cells gamma radiation LD 50 was 435Gy. (author)

  18. High performance liquid chromatography determination of theobromine and caffeine in cocoa beans gamma irradiated

    International Nuclear Information System (INIS)

    Soares, Anderson D.B.; Mansur Neto, Elias

    1997-01-01

    Irradiation is a processing technology that has been shown to be a wholesome process by many scientific studies conducted worldwide during the past 40 years, which has been approved by 37 countries. Irradiated foods have been studied so extensively, that the effects on foods are better understood than any other preservation process, including food freezing and dehydration. Cocoa beans has been commercially irradiated in countries such as Ivory Coast and Argentina. The alkaloids theobromine and caffeine are responsible for the mildly stimulating properties and bitter taste of cocoa and chocolate products. Previously fermented dried and nonfumigated cocoa beans were irradiated at doses of 0, 5.0, 10.0 and 20.0 kGy using Co-60 gamma rays. The samples were analysed for determining theobromine and caffeine contents in the cocoa beans by TIMBIE et al. (1978) high performance liquid chromatography (HPLC) method. Boiling water extracts were cooled, centrifuged and injected into the chromatograph. Theobromine and caffeine were quantitated at 273 nm and showed the tendency of decreasing as the dose of radiation increases. Theobromine and caffeine ranged from 42.3 to 37.1 mg/g and from 7.60 to 6.13 mg/g. respectively from 0 to 20.0 kGy. These results were discussed in relation to the possible acceptance of radiosterization of cocoa beans commercially up to the dose of 20.0 kGy. (author). 10 refs., 1 tab

  19. Gamma ray spectrometry logs as a hydrocarbon indicator for clastic reservoir rocks in Egypt

    International Nuclear Information System (INIS)

    Al-Alfy, I.M.; Nabih, M.A.; Eysa, E.A.

    2013-01-01

    Petroleum oil is an important source for the energy in the world. The Gulf of Suez, Nile Delta and South Valley are important regions for studying hydrocarbon potential in Egypt. A thorium normalization technique was applied on the sandstone reservoirs in the three regions to determine the hydrocarbon potentialities zones using the three spectrometric radioactive gamma ray-logs (eU, eTh and K% logs). The conventional well logs (gamma-ray, deep resistivity, shallow resistivity, neutron, density and sonic logs) are analyzed to determine the net pay zones in these wells. Indices derived from thorium normalized spectral logs indicate the hydrocarbon zones in petroleum reservoirs. The results of this technique in the three regions (Gulf of Suez, Nile Delta and South Valley) are in agreement with the results of the conventional well log analyses by ratios of 82%, 78% and 71% respectively. - Highlights: ► The positive DRAD values indicate the hydrocarbon zones in petroleum reservoirs. ► Thorium normalization was applied to determine the hydrocarbon potentialities. ► The conventional well logs are analyzed to determine the net pay zones in wells. ► Determining hydrocarbon potentialities zones using spectrometric gamma-ray logs

  20. Determination of conversion factors due to the direct and backscattered emission of terrestrial photons gamma

    International Nuclear Information System (INIS)

    Askri, Boubaker

    2008-01-01

    In this thesis we are based on physical criteria to develop a model describing the ground by an optimized geometry in the Monte Carlo simulation of the emission of gamma radiation on earth. This geometry has a unique parameter soil depth. This geometry has been tested successfully. It produced more than 98 pour cent of absorbed dose rate in air at one meter from the ground level and 100 pour cent of the flow line for a uniform distribution of the source and more than 99 pour cent of absorbed dose rate for an exponential distribution source. A considerable gain in computing time compared to classical models was achieved. The backscattered component is more important for low energies than for high-energy emission. By applying the optimized model of soil-air, it reached 100 pour cent of absorbed dose rate in air at a reduced computational time. The conversion factors of dose rate for both filiations natural uranium and thorium were determined by simulation with the optimized geometry. A good agreement was achieved with the values published in the literature. To test this model experimentally, it was necessary to transform the spectrum acquired by a portable germanium detector in a distribution of energy flux of photons to calculate the dose rate experiment. That's why we propose a method for calibration of portable germanium detector by Monte Carlo simulation. In this method, we used a model of diffusion of lithium in germanium to find the thickness of the dead layer of germanium crystal, a parameter not available with precision by the detector. On the basis of the conversion factors calculated using the optimized geometry and the data sampling conducted in the soil of the National Center for Nuclear Science and Technology in Tunis, the value of dose rate was calculated. This value is close to the experimental value of dose rate, which presents the first experimental validation. The optimization made to geometry was used to simulate an aspect related to the spread of

  1. Evaluation of 210Pb air activity concentration by direct gamma-ray spectrometry of air particulate samplings

    International Nuclear Information System (INIS)

    Rizzo, S.; Tomarchio, E.

    2007-01-01

    Main measurement techniques adopted to evaluate 210 PB air activity concentration differ in analysis and sample preparation methods. Some of them involved complex chemical processes or decay product detection (for example 210 Po), with a long decay time period between sampling and experimental measurement. The availability of a low-background gamma-ray spectrometric system, suitable to measure low-energy gamma radiations, allows the evaluation of 210 PB air activity concentration by direct gamma countings of particulate samplings after a short time period from the end of the sampling. The measurement procedure described in this work consists in the following steps: o Sampling of air particulate and recording of sampling data; o Fast reduction of the sample to measurement geometry; o Gamma-ray spectrometric measurement (or a series of measurements) after a minimum decay time period from the end of sampling; o A new gamma-ray spectrometric measurement, with reference to 46.5 keV gamma emission of 210 PB, after a few days from the sampling; o Comparison with a model to evaluate the 210 PB activity percentage produced by decay of short-lived radon daughters on the filter matrix during and after the sampling; o Determination of 210 PB net activity and derived air concentration. Experimental tests have allowed obtaining a range of 2†10 per cent for 210 PB activity percentage on a filter due to decay of short-lived radon daughters, with higher values when 210 PB air activity concentration is very low. All the measurements resulted above detection limit, even in the case of a short sampling time period. A statistical improvement on 210 PB activity can be obtained with a longer sampling time period, without any modification on the procedure and results. (Author)

  2. Committed effective dose determination in cereal flours by gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Scheibel, Viviane

    2006-01-01

    The health impact from radionuclides ingestion of foodstuffs was evaluated by the committed effective doses determined in commercial samples of South-Brazilian cereal flours (soy, wheat, corn, manioc, rye, oat, barley and rice flour). The radioactivity traces of 228 Th, 228 Ra, 226 Ra, 40 K, 7 Be and 137 Cs were measured by gamma-ray spectrometry employing a 66% relative efficiency HPGe detector. The energy resolution for the 1332.46 keV line of 60 Co was 2.03 keV. The committed effective doses were calculated with the activities analyzed in the present flour samples, the foodstuff rates of consumption (Brazilian Institute of Geography and Statistics) and the ingestion dose coefficients (International Commission of Radiological Protection). The reliability median activities were verified with χ 2 tests, assuring the fittings quality. The highest concentration levels of 228 Th and 40 K were 3.5 ± 0.4 and 1469 ± 17 Bq.kg -1 for soy flour, respectively, with 95% of confidence level. The lower limit of detection for 137 Cs ranged from 0.04 to 0.4 Bq.kg -1 . The highest committed effective dose was 0.36 μSv.y -1 for 228 Ra in manioc flour (adults). All committed effective doses determined at the present work were lower than the UNSCEAR limits of 140 μSv.y -1 and much lower than the ICRP (1991) limits of 1 mSv.y -1 , for general public. There are few literature references for natural and artificial radionuclides in foodstuffs and mainly for committed effective doses. This work brings the barley flour data, which is not present at the literature and 7 Be data which is not encountered in foodstuffs at the literature, besides all the other flours data information about activities and committed effective doses. (author)

  3. 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

  4. Environmental levels of gamma emitting radionuclides at PINSTECH

    International Nuclear Information System (INIS)

    Faruq, U.; Parveen, N.; Aziz, A.

    1981-01-01

    Sampling and gamma spectrometric analysis of air-borne particulates and various items of food were carried out at PINSTECH. Air-particulates were analyzed on a computer-based high resolution Ge(Li) detector gamma spectrometer. Food samples were analyzed by a NaI(TI) scintillation detector gamma spectrometer without computer analysis. Data on the levels of the concentration of gamma emitting radionuclides in environmental media at PINSTECH during 1979-80 is given and discussed. (authors)

  5. 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)

  6. Geochemical interpretation of gamma-ray spectrometry images from the Achala granite (Cordoba, Argentina)

    International Nuclear Information System (INIS)

    Lopez, Luis E.

    1998-01-01

    Data of an old spectrometry gamma-ray survey carried out in the Sierras Pampeanas Range by the National Atomic Energy Commission (Argentina) were reprocessed to obtain a corrected digital archive. The geochemical interpretation of the 250 x 250 meters spectrometric grids from the Achala batholith area was based on the behaviour of the radioelements in a peraluminous magma. Spectrometric maps of potassium, uranium, thorium and their ratios were used. In particular, the Th grid was very useful to define the primary magmatic evolution of the granitoids. K and U correlate roughly with Th distribution. The observed positive correlation between Th and U is thought to be the result of surficial leaching of U from uraninite. Finally, U/Th ratio allows to determine both, the magmatic evolution of the rocks and the mineral phase responsible for U content. (author)

  7. Determination of hydrogen in geochemical samples by neutron-induced prompt gamma-ray analysis

    International Nuclear Information System (INIS)

    Shunsuke Yamazaki; Yasuji Oura; Mitsuru Ebihara

    2005-01-01

    Introduction: Hydrogen plays an important role during the evolution of magma. So, water concentrations in rocks are very interesting. Typical quantitative methods for water in rock samples are gravimetry and infrared (IR) spectrometry. In gravimetry, conditions of drying (time, temperature, pressure and atmosphere) must be carefully specified. In IR method, highly hygroscopic reagent must be used to prepare a sample for IR measurement. Neutron-induced prompt gamma-ray analysis (PGA) is a non-destructive method and has high sensitivity for hydrogen. These are special advantages in analyzing valuable specimens such as archaeological samples and meteorite samples. In this study, we aimed to set up an analytical procedure for the determination of hydrogen in rock samples by PGA. Several factors controlling the background and the blank level of hydrogen were evaluated and experimental conditions were fixed. After setting up whole analytical conditions, the procedure was applied to geochemical reference samples and meteorite samples. Comparing our data with recommended and literature values, we evaluate our procedure from a viewpoint of analytical reliability. Experimental: Background level of hydrogen in the atmosphere in a sample holder box was measured by changing a flow rate of helium gas. In addition, the blank level of hydrogen in use of FEP film was evaluated by changing the number of sheets of FEP film. Following these experiments, calibration curve of hydrogen was drawn by irradiating known amounts of potassium hydrogen phthalate (PHP). Then, the procedure was applied to geochemical reference samples. After a constant weight of each sample was reached by drying in an oven at 110 degree C to remove adsorbing moisture, the sample was immediately sealed in a FEP film bag. Samples were irradiated by thermal neutron for about three hours at JRR-3 of JAERI and prompt gamma-rays were measured. Results and Discussion: The background level of hydrogen was determined by

  8. Radiochemical determination of 210Pb using crown ether

    International Nuclear Information System (INIS)

    Vajda, N.; Bodizs, D.; Vodicska, M.

    1994-01-01

    Gamma spectrometric determination of 210 Pb following chemical separation has been performed very precisely and with high sensitivity, due to the low and constant self-absorption of the chemically pure sample. A simple and quick method for the chemical separation of lead using crown ether has been developed. Its four steps are described in detail. The new method was verified using phosphate ore and gypsum samples that were measured in an interlaboratory comparison and with a standard reference material. This method can also be used for self-absorption correction in direct gamma spectrometry of 210 Pb. (N.T.) 4 refs.; 2 figs.; 2 tabs

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

    Energy Technology Data Exchange (ETDEWEB)

    Al-Azmi, Darwish [Department of Applied Sciences, College of Technological Studies, Public Authority for Applied Education and Training, Shuwaikh, P.O. Box: 42325, Code 70654 (Kuwait)]. E-mail: dalazmi@paaet.edu.kw; Karunakara, N. [University Science Instrumentation Centre, Mangalore University, Mangalagangotri 574 199, Mangalore (India)]. E-mail: karunakara_n@yahoo.com

    2007-03-15

    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 {sup 214}Pb and the {sup 214}Bi radon progeny are considered for the detection of the {sup 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.

  10. 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

  11. 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

  12. Radon fixation for determination of {sup 224}Ra, {sup 226}Ra and {sup 228}Ra via gamma-ray spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Herranz, M. [Departamento Ingenieria Nuclear y Mecanica de Fluidos, E. S. Ingenieros de Bilbao - Universidad del Pais Vasco (UPV/EHU), Alda. Urquijo s/n, 48013 Bilbao (Spain)]. E-mail: inphesom@bi.ehu.es; Idoeta, R. [Departamento Ingenieria Nuclear y Mecanica de Fluidos, E. S. Ingenieros de Bilbao - Universidad del Pais Vasco (UPV/EHU), Alda. Urquijo s/n, 48013 Bilbao (Spain); Abelairas, A. [Departamento Ingenieria Nuclear y Mecanica de Fluidos, E. S. Ingenieros de Bilbao - Universidad del Pais Vasco (UPV/EHU), Alda. Urquijo s/n, 48013 Bilbao (Spain); Legarda, F. [Departamento Ingenieria Nuclear y Mecanica de Fluidos, E. S. Ingenieros de Bilbao - Universidad del Pais Vasco (UPV/EHU), Alda. Urquijo s/n, 48013 Bilbao (Spain)

    2006-04-15

    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.

  13. Determination and quantification of impurities found in samples of 124I using gamma spectrometry

    International Nuclear Information System (INIS)

    Silva, Ronaldo Lins da; Delgado, Jose Ubiratan; Araujo, Miriam Taina Ferreira de; Laranjeira, Adilson da Silva; Poledna, Roberto; Veras, Eduardo de; Almeida, Maria Candida M.; Braghirolli, Ana Maria S.

    2014-01-01

    124 I, positron emitter is produced in the IEN/CNEN-RJ and used in diagnosis image of tumors. In this radioisotope production process impurities appear and health agency requires that the level of these characteristics is quantified. These radionuclides emit gamma and X-radiation, allowing the identification and quantitation by gamma spectrometry. With the use of HPGE detector, coupled with the efficiency curve, was identified 125 I and 126 I. The impurity levels measured in the sample were in the range of 0.5% to 90%, respectively, indicating the feasibility of the method for controlling the quality of the radiopharmaceutical

  14. Physical grounds for application of scattered gamma radiation to determine the diameter of casing columns

    International Nuclear Information System (INIS)

    Gulin, Yu.A.; Bernshtejn, D.A.; Khamatdinov, R.T.; Dyad'kin, I.G.

    1976-01-01

    Physical principles of the design of a gamma flow detector for precise measurement of the inside diameter of casing columns with the use of scattered gamma radiation are considered. The design parameters are estimated of a probe ensuring the preassigned (15-18 mm) depth of investigation, which allows to eliminate the effect of external corrosion of the column and that of the substance in the out-of-tube space. Calculations by the Monte Carlo method were made in order to select the optimum parameters of the probe and the radiation energy. As a result of the analysis, design recommendations are made

  15. Determination of Carbamate and Organophosphorus Pesticides in Vegetable Samples and the Efficiency of Gamma-Radiation in Their Removal

    Directory of Open Access Journals (Sweden)

    Muhammed Alamgir Zaman Chowdhury

    2014-01-01

    Full Text Available In the present study, the residual pesticide levels were determined in eggplants (Solanum melongena (n=16, purchased from four different markets in Dhaka, Bangladesh. The carbamate and organophosphorus pesticide residual levels were determined by high performance liquid chromatography (HPLC, and the efficiency of gamma radiation on pesticide removal in three different types of vegetables was also studied. Many (50% of the samples contained pesticides, and three samples had residual levels above the maximum residue levels determined by the World Health Organisation. Three carbamates (carbaryl, carbofuran, and pirimicarb and six organophosphates (phenthoate, diazinon, parathion, dimethoate, phosphamidon, and pirimiphos-methyl were detected in eggplant samples; the highest carbofuran level detected was 1.86 mg/kg, while phenthoate was detected at 0.311 mg/kg. Gamma radiation decreased pesticide levels proportionately with increasing radiation doses. Diazinon, chlorpyrifos, and phosphamidon were reduced by 40–48%, 35–43%, and 30–45%, respectively, when a radiation strength of 0.5 kGy was utilized. However, when the radiation dose was increased to 1.0 kGy, the levels of the pesticides were reduced to 85–90%, 80–91%, and 90–95%, respectively. In summary, our study revealed that pesticide residues are present at high amounts in vegetable samples and that gamma radiation at 1.0 kGy can remove 80–95% of some pesticides.

  16. 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

  17. 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.

  18. Critical analysis of soil hydraulic conductivity determination using monoenergetic gamma radiation attenuation

    International Nuclear Information System (INIS)

    Portezan Filho, Otavio

    1997-01-01

    Three soil samples of different textures: LVA (red yellow latosol), LVE (dark red latosol) and LRd (dystrophic dark red latosol) were utilized for unsaturated hydraulic conductivity K(θ) measurements. Soil bulk densities and water contents during internal water drainage were measured by monoenergetic gamma radiation attenuation, using homogeneous soil columns assembled in the laboratory. The measurements were made with a collimated gamma beam of 0.003 m in diameter using a Nal(Tl) (3'' x 3 '') detector and a 137 Cs gamma source of 74 X 10 8 Bq and 661.6 KeV. Soil columns were scanned with the gamma beam from 0.01 to 0.20 m depth, in 0.01m steps, for several soil water redistribution times. The results show a great variability of the unsaturated hydraulic conductivity relation K(θ), even though homogeneous soils were used. The variability among methods is significantly smaller in relation to variability in space. The assumption of unit hydraulic gradient during redistribution of soil water utilized in the methods of Hillel, Libardi and Sisson leads to hydraulic conductivity values that increase in depth. The exponential character of the K(θ) relationship, is responsible for the difficulty of estimating soil hydraulic conductivity, which is a consequence of small variations in the porous arrangement, even in samples supposed to be homogeneous. (author)

  19. Determination of Proton dose distal fall-off location by detecting right-angled prompt gamma rays

    International Nuclear Information System (INIS)

    Seo, Kyu Seok

    2006-02-01

    The proton beam has a unique advantage over the electron and photon beams in that it can give very high radiation dose to the tumor volume while effectively sparing the neighboring healthy tissue and organs. The number of proton therapy facility is very rapidly increasing in the world. And now the 230 MeV cyclotron facility for proton therapy is constructing at National Cancer Center, this facility until 2006. The distal fall-off location of proton beam is simply calculated by analytical method, but this method has many uncertain when anatomical structure is very complicated. It is very important to know the exact position of the proton beam distal fall-off, or beam range, in the patient's body for both the safety of the patient and the effectiveness of the treatment itself. In 2003, Stichelbaut and Jongen reported the possibility of using the right-angled prompt gamma rays, which are emitted at 90 .deg. from the incident proton beam direction, to determine the position of the proton beam distal fall-off. They studied the interactions of the protons and other secondary particles in a water phantom and concluded that there is a correlation between the position of the distal fall-off and the distribution of the right-angled prompt gamma rays. We have recently designed a prompt gamma scanning system to measure the proton range in situ by using Monte Carlo technique employing MCNPX, FLUKA, and Sabrina TM . The prompt gamma scanning system was designed to measure only the right-angled prompt gamma rays passing through a narrow collimation hole in order to correlate the position with the dose distribution. The collimation part of the scanning system, which has been constructed to measure the gamma rays at 70 MeV of proton energy, is made of a set of paraffin, boron carbide, and lead layers to shield the high-energy neutrons and secondary photons. After the different proton energies and SOBP beam widths are irradiated at the water phantom. we detected prompt gamma at 5 cm

  20. Application of TIMS in isotope correlations for determining the isotope ratios of plutonium

    International Nuclear Information System (INIS)

    Alamelu, D.; Aggarwal, S.K.

    2003-01-01

    Thermal ionisation mass spectrometry (TIMS) is a well-recognized technique for determining the isotopic composition of Pu in irradiated nuclear fuel samples. Other mass spectrometric methods such as ICPMS, SIMS can also be employed for the isotopic analysis of Pu. In the event of non-availability of a mass spectrometer, other techniques such as gamma spectrometry and alpha spectrometry can also be used. They have a limited applicability since data on all the Pu isotopes cannot be obtained

  1. Determination of soil parameters during the water horizontal infiltration and redistribution by gamma ray attenuation method and tensiometry

    International Nuclear Information System (INIS)

    Oliveira, J.C.M. de.

    1991-04-01

    The present work studies the water diffusivity and hydraulic conductivity in a Latossolo Roxo distrofico soil, during the water infiltration and redistribution processes. Variation water flow equations were utilized for the calculations. The data of wetting front positions and of soil water content profiles were obtained through the gamma ray attenuation from a 241-Am source, with 100 mCi activity detected by a standard electronic equipment of gamma spectrometry, with NaI CTD scintillation detector. From the soil water content data in function of space and time and from analytic models, the properties of soil water diffusivity and soil hydraulic conductivity were determined in the laboratory for the 0-10 cm and 10-25 soil layers. (author)

  2. Determination of the cork bark porosity through the gamma ray transmission technology and electronic scanning microscopy image analysis

    International Nuclear Information System (INIS)

    Moraes, Antonio M.C.; Moreira, Anderson C.; Appoloni, Carlos R.

    2007-01-01

    This work applies the gamma transmission techniques (GTR) and imaging by scanning electron microscopy (SEM) for determination of porosity in the sparkling wine bottle corks. The gamma transmission experimental apparatus consists of a micrometric table (ZX) of sample movement automated, a Am-241 source (59,53 keV, 100 mCi), lead collimators, sample-holder, Na I(Tl) detector and appropriated electronics. For the microscopic images an FEI (Quanta 200), electronic microscope with associated electronics was used, and the image analysis was performed with IMAGO software. The average porosity for 22 samples analysed by GTR was of φ=58 +- 4.6 percent. By the imaging technique the found average porosity was φ=60.0 +- 6.2 percent. (author)

  3. Gamma spectrometry in the Osiris reactor. Determination of the power and burn-up rate of irradiated fuel element

    International Nuclear Information System (INIS)

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

    1976-01-01

    The gamma spectrometry facility, original in design, located in the immediate proximity of the OSIRIS reactor core at Saclay, is described. This device is used to examine nuclear fuel elements irradiated in OSIRIS or in some power reactors. In most cases, it is possible to equip power reactors (in particular water reactors) with installations of this type. With this device, it is also possible to follow the evolution of a large number of fission products in space and time, and to obtain useful information concerning nuclear safety (for example, cladding rupture) and fuel economy (with burn-up rate determination). Details on the performance of this measuring device are given in connection with the study of burn-up rates and linear irradiation power. This OSIRIS reactor gamma spectrometry installation is a nondestructive testing technique, which is easy and rapid to use [fr

  4. Density determination in Pino Radiata (D.Don) samples using 59.5 keV gamma radiation attenuation

    International Nuclear Information System (INIS)

    Dinator, Maria I.; Morales, Jose R.; Aliaga, Nelson; Karsulovic, Jose T.; Sanchez, Jaime; Leon, Adolfo

    1996-01-01

    A non destructive method to determine wood samples density is presented. The photon mass attenuation coefficient in samples of Pino radiata (D.Don) was measured at 59.5 keV with a radioactive source of Am-241. The value of 0.192 ± 0.002 cm 2 /g was obtained with a gamma spectroscopy system and later used on the determination of the mass density in sixteen samples of the same species. Comparison of these results with those of gravimetric method through a linear regression showed a slope of 1.001 and a correlation factor of 0.94. (author)

  5. A novel approach to the determination of iridium via Ge-coincidence/NaI(Tl)-anticoincidence gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Cumming, J.B.

    1988-01-01

    Iridium has proven to be a useful fingerprint of extraterrestrial material, and neutron activation analysis is the method of choice for its determination because of the high thermal cross section (910 b) of 191 Ir (37.3% natural abundance) and the favorable decay characteristics of the product nuclide. However, radiochemical separations are frequently required for the determination of iridium at low concentrations (in the ppb range). The present work describes a precise, nondestructive neutron-activation procedure that is capable of analyzing samples of both high (ppm) and low (ppb) Ir content. Advantage is taken of the fact that the principal gamma lines of 73.8-d 192 Ir are in various coincidences with one another. Instead of conventional gamma-gamma coincidence spectrometry with two Ge detectors, we utilize the 784.6- and 920.9- keV sum peaks which are generated when an iridium containing sample is placed in the well of a highly-efficient HPGe detector. The well-type detector is positioned centrally in a large annular NaI(Tl) detector which is operated in an anticoincidence mode. This improves the quality of the gamma spectra by suppressing the Compton backgrounds due to nuclides such as 60 Co by a factor of 4-6 in the regions of interest without affecting the intensities of the two sum peaks. The sensitivity of this method under our experimental conditions (20-mg sample irradiated at 1.5x10 14 n cm -2 s -1 for 5 min and counted 3-4 weeks after irradiation) is ≅ 5 ppb Ir in a relatively unfavorable matrix such as peridotite. (orig.)

  6. Standard test methods for chemical, mass spectrometric, spectrochemical, nuclear, and radiochemical analysis of nuclear-grade plutonium metal

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2004-01-01

    1.1 These test methods cover procedures for the chemical, mass spectrometric, spectrochemical, nuclear, and radiochemical analysis of nuclear-grade plutonium metal to determine compliance with specifications.

  7. The life and death of massive stars revealed by the observation of nuclear gamma-ray lines with the Integral/SPI spectrometer; La vie et la mort des etoiles massives revelees par l'observation des raies gamma nucleaires grace au spectrometre INTEGRAL/SPI

    Energy Technology Data Exchange (ETDEWEB)

    Martin, P

    2008-11-15

    The aim of this research thesis is to bring up observational constraints on the mechanisms which govern life and death of massive stars, i.e. stars having an initial mass greater than eight times the Sun's mass, and smaller than 120 to 150 solar masses. Thus, it aims at detecting the vestiges of recent and close supernovae in order to find out the traces of the dynamics of their first instants. The author has explored the radiation of three radio-isotopes accessible to the nuclear gamma astronomy ({sup 44}Ti, {sup 60}Fe, {sup 26}Al) using observations performed with high resolution gamma spectrometer (SPI) on the INTEGRAL international observatory. After an overview of the present knowledge on the massive star explosion mechanism, the author presents the specificities and potential of the investigated radio-isotopes. He describes the data treatment methods and a population synthesis programme for the prediction of decay gamma streaks, and then reports its work on the inner dynamics of Cassiopeia A explosion, the stellar activity of the galaxy revealed by the radioisotope observation, the nucleo-synthetic activity of the Swan region.

  8. Feasibility study of photodiodes utilization in the soil-moisture determination by gamma transmission

    International Nuclear Information System (INIS)

    Santos, L.A.P. dos.

    1992-08-01

    This study was done to verify the viability of photodiodes, as gamma radiation detector ( 241 Am - Energy=60 KeV), to measure soil water content. The photodiodes used had different mechanical and electrical characteristics, and were tested on soils of different textures. A good linear correlation between the logarithm of the attenuation factor and soil-moisture demonstrated such viability, and that the low photopeak efficiency of these devices is not a limitation to the measurement of soil water content. Furthermore, the stability, the portability, and low cost of such semiconductor devices, including its electronic system, represent relevant characteristics that may justify the development of a reliable gamma meter system for field studies. (author). 37 refs, 21 figs, 20 tabs

  9. A General Analysis of $\\gamma$ Determinations from $B \\to \\pi K$ Decays

    CERN Document Server

    Buras, Andrzej J; Buras, Andrzej J.; Fleischer, Robert

    1999-01-01

    We present a general parametrization of $B^\\pm\\to\\pi^\\pm K, \\pi^0K^\\pm$ and $B_d\\to\\pi^0 K, \\pi^\\mp K^\\pm$ decays, taking into account both electroweak penguin and rescattering effects. This formalism allows -- among other things -- an improved implementation of the strategies that were recently proposed by Neubert and Rosner to probe the CKM angle $\\gamma$ with the help of $B^\\pm\\to\\pi^\\pm K, \\pi^0K^\\pm$ decays. In particular, it allows us to investigate the sensitivity of the extracted value of $\\gamma$ to the basic assumptions of their approach. We find that certain SU(3)-breaking effects may have an important impact and emphasize that additional hadronic uncertainties are due to rescattering processes. The latter can be controlled by using SU(3) flavour symmetry arguments and additional experimental information provided by $B^\\pm\\to K^\\pm K$ modes. We propose a new strategy to probe the angle $\\gamma$ with the help of the neutral decays $B_d\\to\\pi^0 K, \\pi^\\mp K^\\pm$, which is theoretically cleaner than t...

  10. Gamma-ray spectrometric analyses of some Nigerian rock samples

    International Nuclear Information System (INIS)

    Uwah, E.J.; Ajakaiye, D.E.

    1990-01-01

    Approximate uranium concentrations in rock samples from the Sokoto Basin of Nigeria were predicted from γ-equivalent uranium and thorium (eU and eTh) measurements which made use of similar rock samples, previously analyzed by delayed neutron counting (DNC) and x-ray fluorescence (XRF) techniques, as reference materials. Comparison of the results of the 3 techniques shows that the eU values approximate the DNC results more than the XRF results do, with standard error of estimate of ±6.68 ppm eU and correlation coefficient of 0.984. Corresponding values for XRF analyses are ±32.53 ppm U and 0.730, respectively. (author)

  11. Automation of low energy gamma spectrometric analysis of mineral samples

    International Nuclear Information System (INIS)

    Padilla, R.; Gonzalez, J.

    1996-01-01

    An interface device to perform the automatic operation of a multichannel analyser CANBERRA S30 from a COMODORE 64 microcomputer was developed. The interface also allows the manual control of the MCA and fulfills the requirements of low cost and simplicity

  12. Development of an open source software of quantitative analysis for radionuclide determination by gamma-ray spectrometry using semiconductor detectors

    International Nuclear Information System (INIS)

    Maduar, Marcelo Francis

    2010-01-01

    Radioactivity quantification of gamma-ray emitter radionuclides in samples measured by HPGe gamma-ray spectrometry relies on the analysis of the photopeaks present in the spectra, especially on the accurate determination of their net areas. Such a task is usually performed with the aid of proprietary software tools. This work presents a methodology, algorithm descriptions and an open source application, called OpenGamma, for the peak search and analysis in order to obtain the relevant peaks parameters and radionuclides activities. The computational implementation is released entirely in open-source license for the main code and with the use of open software packages for interface design and mathematical libraries. The procedure for the peak search is performed on a three step approach. Firstly a preliminary search is done by using the second-difference method, consisting in the generation of a derived spectrum in order to find candidate peaks. In the second step, the experimental peaks widths are assessed and well formed and isolated ones are chosen to obtain a FWHM vs. channel relationship, by application of the Levenberg-Marquardt minimization method for non-linear fitting. Lastly, regions of the spectrum with grouped peaks are marked and a non-linear fit is again applied to each region to obtain baseline and photopeaks terms; from these terms, peaks net areas are then assessed. (author)

  13. DETERMINATION OF MICROBE CONTAMINANT IN CENTELLA ASIATICA SIMPLISIA AND EXTRACT BEFORE AND AFTER GAMMA-RAYS PASTEURIZATION

    Directory of Open Access Journals (Sweden)

    Eriawan Rismana

    2015-05-01

    Full Text Available Determination of microbe content in the Centella asiatica simplisia and extractbefore and after pasteurization process by Gamma-rays with variation of dose has been evaluated. The radiation process into the simplisia and extract significantly decreased of microbe content from > 104 to < 10 - 100 colonies. For the various radiation dose at 2.5 – 10.0 kGy, the decreased microbe content in the extract to < 10 colonies. The result showedthat the radiation to extract was more effectively than to simplisia, in the decrease of microbe contaminant. The result of TLC analysis showed that the radiation was not affected to the active compound in extract.

  14. Determination of the dose rate to the center of the irradiation chamber of the Gamma cell 220 AECL

    International Nuclear Information System (INIS)

    Zuazua G, M.P.

    1991-11-01

    To determine the dose rate at the center of the irradiation chamber of the Gamma cell 220 AECL, two different spectrophotometers for to measure the absorbency of the irradiated dosemeters were used. In the first one dosimetry, the absorbency of the irradiated Fricke solution was read in the Varian-UV-visible spectrophotometer Series 634 of the Applied Research Management. For the second dosimetry it was used the Shimadzu UV-visible spectrophotometer belonging to the Special Projects Department. The obtained results in this study are presented. (Author)

  15. Determination of the 121Te gamma emission probabilities associated with the production process of radiopharmaceutical NaI[123I

    International Nuclear Information System (INIS)

    De Araújo, M T F; Poledna, R; Delgado, J U; De Almeida, M C M; Silva, R L; Lopes, R T; Cagido, A C F

    2016-01-01

    The 123 I is widely used in radiodiagnostic procedures in nuclear medicine. According to Pharmacopoeia care should be taken during its production process, since radionuclidic impurities may be generated. The 121 Te is an impurity that arises during the 123 I production and determining their gamma emission probabilities (Pγ) is important in order to obtain more information about its decay. Activities were also obtained by absolute standardization using the sum-peak method and these values were compared to the efficiency curve method. (paper)

  16. 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

  17. Study and validation of a gamma-ray spectrometer for the remote analysis of the chemical composition of planetary surfaces: application to a mission to the planet Mercury; Etude et validation d'un spectrometre gamma pour la mesure de la composition chimique des surfaces planetaires

    Energy Technology Data Exchange (ETDEWEB)

    Pirard, B

    2006-12-15

    This work deals with the design of a gamma-ray spectrometer for the remote analysis of the chemical composition of planetary surfaces and was performed in the frame of a mission scenario to explore the planet Mercury. The research studies consisted first in characterizing the detection performances of a gamma-ray spectrometer using a high-purity germanium crystal cooled actively at cryogenic temperatures. The high energy resolution of the detector allows an accurate measurement of the chemical composition for the main elements from oxygen to uranium. Thereafter the studies dealt with the critical issues addressed for the use of such a detector onboard a mission to the inner solar system. The radiation damage caused by solar protons in germanium crystals was investigated by experimental and numerical means. It has been shown that the detector resolution begins getting damaged for proton fluences over 5*10{sup 8} p/cm{sup 2}. An annealing session where the crystal is heated up to 80 C degrees for a 4-day period allows the detector to get back a sufficient resolution. Annealing over 100 C degrees gives back the detector its initial resolution. Finally, a numerical thermal model of the instrument as well as some tests on a thermal mockup were performed to validate the thermal design of the instrument.

  18. 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

  19. Shielding application of perturbation theory to determine changes in neutron and gamma doses due to changes in shield layers

    Science.gov (United States)

    Fieno, D.

    1972-01-01

    Perturbation theory formulas were derived and applied to determine changes in neutron and gamma-ray doses due to changes in various radiation shield layers for fixed sources. For a given source and detector position, the perturbation method enables dose derivatives with respect to density, or equivalently thickness, for every layer to be determined from one forward and one inhomogeneous adjoint calculation. A direct determination without the perturbation approach would require two forward calculations to evaluate the dose derivative due to a change in a single layer. Hence, the perturbation method for obtaining dose derivatives requires fewer computations for design studies of multilayer shields. For an illustrative problem, a comparison was made of the fractional change in the dose per unit change in the thickness of each shield layer in a two-layer spherical configuration as calculated by perturbation theory and by successive direct calculations; excellent agreement was obtained between the two methods.

  20. Integration of auto analysis program of gamma spectrum and software and determination of element content in sample by k-zero method

    International Nuclear Information System (INIS)

    Trinh Quang Vinh; Truong Thi Hong Loan; Mai Van Nhon; Huynh Truc Phuong

    2014-01-01

    Integrating the gamma spectrum auto-analysis program with elemental analysis software by k-zero method is the objective for many researchers. This work is the first stepin building an auto analysis program of gamma spectrum, which includes modules of reading spectrum, displaying spectrum, calibrating energy of peak, smoothing spectrum, calculating peak area and determining content of elements in sample. Then, the results from the measurements of standard samples by a low level spectrometer using HPGe detector are compared to those of other gamma spectrum auto-analysis programs. (author)

  1. Molecular determinants of desensitization and assembly of the chimeric GABA(A) receptor subunits (alpha1/gamma2) and (gamma2/alpha1) in combinations with beta2 and gamma2

    DEFF Research Database (Denmark)

    Elster, L; Kristiansen, U; Pickering, D S

    2001-01-01

    Two gamma-aminobutyric acid(A) (GABA(A)) receptor chimeras were designed in order to elucidate the structural requirements for GABA(A) receptor desensitization and assembly. The (alpha1/gamma2) and (gamma2/alpha1) chimeric subunits representing the extracellular N-terminal domain of alpha1 or gam...... receptor with respect to the direct activation by pentobarbital. This suggests differences in the mechanism of channel activation for pentobarbital and GABA....

  2. Mercury determination in natural waters using neutron activation analysis

    International Nuclear Information System (INIS)

    Cagnone, M.; Marques, R.O.

    1994-01-01

    Available as short communication only. An analytical method for quantitative determination of Mercury traces in river and sea water is proposed. The neutron activation method and radiochemical separation of Mercury by developing of C L 4 Hg -2 complex, and their chromatographic separation using anionic exchange resin Dowex 1 X 8 of 400 mesh is used. The quantitative determination is done by gamma spectrometric analysis. The selection limits reached with this method showed that this is an amenable procedure in routine mercury determination in the ppb level, specially useful in the environmental contamination analysis. (author). 3 refs, 2 figs, 1 tab

  3. Gamma ray spectrometry logs as a hydrocarbon indicator for clastic reservoir rocks in Egypt.

    Science.gov (United States)

    Al-Alfy, I M; Nabih, M A; Eysa, E A

    2013-03-01

    Petroleum oil is an important source for the energy in the world. The Gulf of Suez, Nile Delta and South Valley are important regions for studying hydrocarbon potential in Egypt. A thorium normalization technique was applied on the sandstone reservoirs in the three regions to determine the hydrocarbon potentialities zones using the three spectrometric radioactive gamma ray-logs (eU, eTh and K% logs). The conventional well logs (gamma-ray, deep resistivity, shallow resistivity, neutron, density and sonic logs) are analyzed to determine the net pay zones in these wells. Indices derived from thorium normalized spectral logs indicate the hydrocarbon zones in petroleum reservoirs. The results of this technique in the three regions (Gulf of Suez, Nile Delta and South Valley) are in agreement with the results of the conventional well log analyses by ratios of 82%, 78% and 71% respectively. Crown Copyright © 2012. Published by Elsevier Ltd. All rights reserved.

  4. Determination of the {eta} mass from the production threshold for the {gamma}p {yields} p{eta} reaction

    Energy Technology Data Exchange (ETDEWEB)

    Nikolaev, Alexander

    2012-09-06

    This thesis is dedicated to a new precise determination of the {eta} meson mass based on a measurement of the threshold for the {gamma}p {yields} p{eta} reaction. This experiment was performed in the years 2004/2005 using the Crystal Ball/TAPS detector setup and the recently developed tagger focal-plane microscope detector at the MAMI-B facility in the Institut fuer Kernphysik of the Johannes Gutenberg-Universitaet Mainz. The real photon beam was produced by Bremsstrahlung of the 883 MeV electrons from MAMI-B on a thin diamond radiator. The {eta} mesons were identified via their two main decay modes, {eta} {yields} 2{gamma} and {eta} {yields} 3{pi}{sup 0}, with the Crystal Ball/TAPS setup, which measured energies and emission angles of particles. The identification of the {eta} {yields} 2{gamma} decay was performed using events with two clusters detected as photons, ignoring all other particles, and the standard invariant mass analysis. Cuts were applied on the invariant and missing mass distributions. The identification of the {eta} {yields} 3{pi}{sup 0} {yields} 6{gamma} decay concentrated on events with six clusters detected as photons. Among fifteen possible combinations of six photons to be arranged in three pairs, the combination with the smallest {chi}{sup 2}-value for the three pion masses was assumed to be correct. Cuts were applied on the {chi}{sup 2}-distribution and on the invariant and missing mass distributions. The normalization of the total cross section was obtained from the target thickness, the intensity of the photon flux, the simulated acceptance of the Crystal Ball, and the branching ratios of the {eta} decays. The determination of the {eta} mass required a very precise measurement of the production threshold. This was obtained by fitting the measured cross section as a function of photon energy and gave the result for the {eta} mass, m{sub {eta}}=(547.851{+-}0.031{sub stat.}{+-}0.062{sub syst.}) MeV.

  5. Determination of changes induced by gamma radiation in nectar of kiwi fruit (Actinidia deliciosa)

    Energy Technology Data Exchange (ETDEWEB)

    Harder, M.N.C.; De Toledo, T.C.F.; Ferreira, A.C.P. [Centro de Energia Nuclear na Agricultura (CENA/USP), Laboratorio de Irradiacao de Alimentos e Radioentomologia, Av. Centenario, 303, Piracicaba CEP 13400-970 Sao Paulo (Brazil); Arthur, V. [Centro de Energia Nuclear na Agricultura (CENA/USP), Laboratorio de Irradiacao de Alimentos e Radioentomologia, Av. Centenario, 303, Piracicaba CEP 13400-970 Sao Paulo (Brazil)], E-mail: arthur@cena.usp.br

    2009-07-15

    The kiwi (Actinidia deliciosa; Actinidaceae) is an exotic fruit to Brazil, introduced from southeastern China. The kiwi fruit presents a high nutritional value, rich mainly in vitamin C and fibers, calcium, iron and phosphorus, which give it an excellent nutritional value. Its quality attributes and flavor has lead to acceptance in consuming markets, mainly among children. The objective of this work was to formulate a non-alcoholic sweetened drink based on kiwi fruits, to submit the drink to gamma radiation using increasing doses: 0 (control), 0.5, 1.0 and 2.0 kGy, and to evaluate changes in physical and chemical quality attributes. We found that no significant difference was observed between treatments relative to the control. So we could conclude that for the doses tested significant alterations in the physiochemical characteristics of the kiwi nectar were introduced.

  6. Determination of changes induced by gamma radiation in nectar of kiwi fruit ( Actinidia deliciosa)

    Science.gov (United States)

    Harder, M. N. C.; De Toledo, T. C. F.; Ferreira, A. C. P.; Arthur, V.

    2009-07-01

    The kiwi ( Actinidia deliciosa; Actinidaceae) is an exotic fruit to Brazil, introduced from southeastern China. The kiwi fruit presents a high nutritional value, rich mainly in vitamin C and fibers, calcium, iron and phosphorus, which give it an excellent nutritional value. Its quality attributes and flavor has lead to acceptance in consuming markets, mainly among children. The objective of this work was to formulate a non-alcoholic sweetened drink based on kiwi fruits, to submit the drink to gamma radiation using increasing doses: 0 (control), 0.5, 1.0 and 2.0 kGy, and to evaluate changes in physical and chemical quality attributes. We found that no significant difference was observed between treatments relative to the control. So we could conclude that for the doses tested significant alterations in the physiochemical characteristics of the kiwi nectar were introduced.

  7. Geographically determined dependencies in the value of the constant natural radiation gamma-background

    International Nuclear Information System (INIS)

    Miloslavov, V.

    2001-01-01

    The problem of the assessment of the influence of natural gamma background changes on the population is discussed. It is considered that the populations in different geographic regions have adapted by evolution mechanisms to the respective unchanged (without human activities) radiation background. The background limits for each area form the 'radiation comfortable zone' which varies very much for the different geographic areas. Leaving the 'comfortable zone' leads to a triggering of adaptive mechanisms in the population including the natural selection in order to reach an equilibrium. Thus, the radiation impact exceeding the 'comfortable zone' is expected to cause harm for a part of the population which is preliminarily burden or uncapable to adapt. From this point of view the increased morbidity due to radiation factor in those cases remains hidden. As a conclusion it is pointed out that the proposed increase of the annual dose for the population might result with harmful consequences for the whole human population

  8. Determination of radiochemical yield of 99mTc radiopharmaceutical preparations using gamma counter and linear radiochromatography scanner

    International Nuclear Information System (INIS)

    Martins, Patricia de A.; Moura, Rebeca G.; Shiki, Andressa M.; Fukumori, Neuza T.O.; Matsuda, Margareth M.N.

    2013-01-01

    The radiochemical purity (RCP) evaluation is a prerequisite for radiopharmaceuticals before the administration in patients. RCP is defined as the proportion of the total radioactivity in the product that is present in the specified chemical form. The most widely used techniques for RCP determination in radiopharmaceutical preparations are thin layer chromatography (TLC-Al), instant thin layer chromatography (ITLC-SG) and paper chromatography (PC). These techniques combined with radioactivity detection are one of the most important tools in the RCP of the radiopharmaceutical compounds. Several methods are used for the determination of the spatial distribution of radioactivity on the strips. The aim of this study was to compare two methods for radioactivity measurement in the determination of RCP in 99m Tc radiopharmaceuticals using gamma counter and linear radiochromatography scanner. Lyophilized radiopharmaceuticals were labeled with 99m Tc. The analysis was carried out using TLC-Al and high performance thin layer chromatography (HPTLC-Cellulose) sheets, ITLC-SG and 3MM Whatman PC. The radioactivity distribution was determined by counting each strip during 1 minute in a radiochromatography TLC scanner. For comparison, the strips were cut into small pieces and each one was separately measured in a gamma-counter during 0.20 minutes in 70-210 KeV 99m Tc window. USP 36 and FDA specify that not less than 90% of the total radioactivity must be in the spot corresponding to 99m Tc labeled compound. In conclusion, the procedure for RCP determination of ALBUMINA-TEC, DEX500-TEC, ECD-TEC, MACRO-TEC and MIBI-TEC can be faster using radiochromatography. (author)

  9. Radio spectrometric survey of un-surveyed areas in Syria

    International Nuclear Information System (INIS)

    Aissa, M.; Al-Hent, R; Jubeli, Y.

    2002-11-01

    The values and distribution of the radioelements e U, e Th, % K and Ur units in the surface geological formations of the west and south sectors of Syrian region, were estimated using carbone gamma ray spectrometric survey. The radiometric maps were prepared, as well as, many geological profiles, cross sections studied in different locations and geochemical samples were analyzed by laboratory gamma ray spectrometry and by x-ray diffractometry, the results of the all sets were compared. In general, the survey shows, low radioelement concentrations in the area, especially on basic rocks (Jabal Al-arab, Hawran) south Syria, and on ultra basic rocks (ophiolitic complex) north-west Syria, but there are some separate anomalous spots were connected with phosphate rocks, detected on cretaceous and Palaeogene age. Some times we noticed high radioelement concentrations haloes associated with fractured zones were already arise from secondary uranium mineralization, as a result of solutions movement through fissures in carbonatic and/or chalk like limestone rocks. finally, the obtained concentrations, represent a background values which has no significant importance for uranium exploration point of view. (author)

  10. Perturbation of pharmacologically relevant polyphenolic compounds in Moringa oleifera against photo-oxidative damages imposed by gamma radiation

    CSIR Research Space (South Africa)

    Ramabulana, T

    2016-03-01

    Full Text Available Moringa oleifera after gamma radiation treatment were investigated with reverse phase liquid chromatography and mass spectrometric techniques in combination with multivariate data models such as principal component analysis and orthogonal projection...

  11. Determination of structural geometric parameters of industrial ceramic foams by gamma rays transmission and X-rays microtomography

    International Nuclear Information System (INIS)

    Rocha, Wilson Roberto Dejato da

    2005-01-01

    In this work, the gamma rays transmission and X-rays microtomography techniques are used for the evaluation of the porosity and the pore size distribution of SiC ceramic foams. It was also accomplished the three-dimensional images after the determination of samples geometric parameters. The geometric parameters were obtained by two-dimensional images analyses, generated by a Microfocus system, with a CCD camera, an images intensifier, a X-rays tube and an automatic system for rotation of the sample. The spatial resolution of the images was about 32 μm. In the gamma rays transmission methodology, a Nal(Tl) scintillation detector, an 241 Am (59.53 keV, 100 mCi) radioactive source and an automatic X-Z micrometric table was used. The analyzed samples had pores density of 30, 45, 60, 80 and 100 ppi (pores per inch). The gamma rays transmission technique was accurate to supply the porosity of the samples, which ranged about 90% and was in agreement with the values supplied by manufacturer of the foams. The 30 and 45 ppi samples analyzed by X-rays microtomography showed porosity results that agree with the average porosity supplied by the manufacturer. In other hand, the 60, 80 and 100 ppi samples systematically showed average porosity about 4%, lower than the average of the manufacturer. The pore size distributions found through the software IMAGO show the presence of smaller pores than those nominated by the manufacturer. The 30 ppi samples had voids inside the solid material of the ceramic foams structure. Gaussian truncated method, used in the three-dimensional reconstruction, was not able to take into the account the voids inside the solid matrix. (author)

  12. Photon Activation Analysis Of Light Elements Using 'Non-Gamma' Radiation Spectroscopy - The Instrumental Determination Of Phosphorus

    International Nuclear Information System (INIS)

    Segebade, Christian; Goerner, Wolf

    2011-01-01

    Unlike metal determinations the analysis of light elements (e.g., carbon, oxygen, phosphorus) is frequently problematic, in particular if analysed instrumentally. In photon activation analysis (PAA) the respective activation products do not emit gamma radiation in the most cases. Usually, annihilation quanta counting and subsequent decay curve analysis have been used for determinations of C, N, O, and F. However, radiochemical separation of the respective radioisotopes mostly is indispensable. For several reasons, some of the light elements cannot be analysed following this procedure, e.g. phosphorus. In this contribution the instrumental PAA of phosphorus in organic matrix by activation with bremsstrahlung of an electron linear accelerator and subsequent beta spectroscopy is described. The accuracy of the results was excellent as obtained by analysis of a BCR Reference Material.

  13. Neutron and gamma-ray transmission technique for the on-line determination of moisture in coal and coke

    International Nuclear Information System (INIS)

    Sowerby, B.D.; Millen, M.J.; Rafter, P.T.

    1985-01-01

    A fast neutron and gamma-ray transmission technique is being developed for the on-line analysis of moisture in coal and coke. The technique utilises 252 Cf and 137 Cs sources and 3 He and NaI(Tl) detectors. Laboratory measurements on single coal samples have shown that moisture can be determined to better than 1 wt% over the range 0 to 16 wt% moisture and 5 to 17cm thickness. Reduced errors were obtained for restricted ranges of moisture and thickness. Preliminary measurements on coke of thickness 30 to 50cm have shown that moisture can be determined to within 0.26 wt% over the range 1 to 16 wt% moisture

  14. Application of the radiochemical - and the direct gamma ray spectrometry method to the burnup determination of irradiated uranium oxide

    International Nuclear Information System (INIS)

    Cunha, I.I.L.

    1979-01-01

    The burn up of natural U 3 O 8 that occurs by the action of thermal neutrons was determined, using the radioisotopes 144 Ce, 137 Cs, 103 Ru, 106 Ru and 95 Zr as monitors. The determination of the burn up was made using both destructive and non-destructive methods. In the non-destructive method, the technique of direct gamma-ray spectrometry was used and the radioisotopes mentioned were simultaneously counted in a Ge-Li detector. In the radiochemical method the same radioisotopes were isolated one from the other and from all other fission products before counting. The solvent extraction technique was used for the radiochemical separation of uranium, cerium, cesium and ruthenium. To separate zirconium and niobium, adsorption in silica-gel was used. The extraction agent employed to isolate cesium was dipycrilamine and for the separation of the other radioisotopes Di-(2-Ethyl Hexyl) Phosphoric acid (HDEHP) was used. (Author) [pt

  15. A semi-empirical approach to determine gamma activities (Bqkg{sup -1}) in environmental cylindrical samples

    Energy Technology Data Exchange (ETDEWEB)

    Palacios, Daniel Francisco [Universidad Simon Bolivar (USB), Apartado 89000, Caracas (Venezuela)], E-mail: palacios@usb.ve; Alfonso, Juan A. [Instituto Venezolano de Investigaciones Cientificas (IVIC), Apartado 21827, Caracas (Venezuela); Barros, Haydn [Universidad Simon Bolivar (USB), Apartado 89000, Caracas (Venezuela); LaBrecque, John J.; Perez, Karla [Instituto Venezolano de Investigaciones Cientificas (IVIC), Apartado 21827, Caracas (Venezuela); Lossada, Marian R. [Direccion de Investigacion y Postgrado, Universidad Maritima del Caribe (UMC), Caracas (Venezuela)

    2008-01-15

    A semi-empirical method to determine radionuclide concentrations in large environmental samples without the use of reference material and avoiding the typical complexity of Monte-Carlo codes is proposed. The calculation of full-energy peak efficiencies was carried out from a relative efficiency curve (obtained from the gamma spectra data), and the geometric (simulated by Monte-Carlo), absorption, sample and intrinsic efficiencies for energies between 130 and 3000 keV. The absorption and sample efficiencies were determined from the mass absorption coefficients, whereas the intrinsic efficiency was approximated by an empirical function. The deviations between calculated and experimental efficiencies for a reference material in most cases are less than 10%. Radionuclide activities in marine sediment samples calculated by the proposed method and by the experimental comparative method were not significantly different. This new method can be used for routine environmental monitoring when uncertainties up to 10% are acceptable.

  16. Assay for uranium and determination of disequilibrium by means of in situ high resolution gamma-ray spectrometry

    Science.gov (United States)

    Tanner, Allan B.; Moxham, Robert M.; Senftle, F.E.

    1977-01-01

    Two sealed sondes, using germanium gamma-ray detectors cooled by melting propane, have been field tested to depths of 79 m in water-filled boreholes at the Pawnee Uranium Mine in Bee Co., Texas. When, used as total-count devices, the sondes are comparable in logging speed and counting rate with conventional scintillation detectors for locating zones of high radioactivity. When used with a multichannel analyzer, the sondes are detectors with such high resolution that individual lines from the complex spectra of the uranium and thorium series can be distinguished. Gamma rays from each group of the uranium series can be measured in ore zones permitting determination of the state of equilibrium at each measurement point. Series of 10-minute spectra taken at 0.3- to 0.5-m intervals in several holes showed zones where maxima from the uranium group and from the 222Rn group were displaced relative to each other. Apparent excesses of 230Th at some locations suggest that uranium-group concentrations at those locations were severalfold greater some tens of kiloyears, ago. At the current state of development a 10-minute count yields a sensitivity of about 80 ppm U308. Data reduction could in practice be accomplished in about 5 minutes. The result is practically unaffected by disequilibrium or radon contamination. In comparison with core assay, high-resolution spectrometry samples a larger volume; avoids problems due to incomplete core recovery, loss of friable material to drilling fluids, and errors in depth and marking; and permits use of less expensive drilling methods. Because gamma rays from the radionuclides are accumulated simultaneously, it also avoids the problems inherent in trying to correlate logs made in separate runs with different equipment. Continuous-motion delayed-gamma activation by a 163-?g 252Cf neutron source attached to the sonde yielded poor sensitivity. A better neutron-activation method, in which the sonde is moved in steps so as to place the detector

  17. Spectrometric mixture analysis: An unexpected wrinkle

    Indian Academy of Sciences (India)

    Administrator

    Dedicated to the memory of the late Professor S K Rangarajan. Spectrometric mixture analysis: An unexpected wrinkle. †. ROBERT DE LEVIE. Chemistry Department ..... For a quick visual check of the mixture spectra, we plotted the absorbances of those solutions that have a constant value of c + t, such as (0, 180), (90,.

  18. Determination of $\\gamma$ and $-2\\beta_s$ from charmless two-body decays of beauty mesons

    CERN Document Server

    Aaij, Roel; Adeva, Bernardo; Adinolfi, Marco; Affolder, Anthony; Ajaltouni, Ziad; Akar, Simon; Albrecht, Johannes; Alessio, Federico; Alexander, Michael; Ali, Suvayu; Alkhazov, Georgy; Alvarez Cartelle, Paula; Alves Jr, Antonio Augusto; Amato, Sandra; Amerio, Silvia; Amhis, Yasmine; An, Liupan; Anderlini, Lucio; Anderson, Jonathan; Andreassen, Rolf; Andreotti, Mirco; Andrews, Jason; Appleby, Robert; Aquines Gutierrez, Osvaldo; Archilli, Flavio; Artamonov, Alexander; Artuso, Marina; Aslanides, Elie; Auriemma, Giulio; Baalouch, Marouen; Bachmann, Sebastian; Back, John; Badalov, Alexey; Baesso, Clarissa; Baldini, Wander; Barlow, Roger; Barschel, Colin; Barsuk, Sergey; Barter, William; Batozskaya, Varvara; Battista, Vincenzo; Bay, Aurelio; Beaucourt, Leo; Beddow, John; Bedeschi, Franco; Bediaga, Ignacio; Belogurov, Sergey; Belous, Konstantin; Belyaev, Ivan; Ben-Haim, Eli; Bencivenni, Giovanni; Benson, Sean; Benton, Jack; Berezhnoy, Alexander; Bernet, Roland; Bettler, Marc-Olivier; van Beuzekom, Martinus; Bien, Alexander; Bifani, Simone; Bird, Thomas; Bizzeti, Andrea; Bjørnstad, Pål Marius; Blake, Thomas; Blanc, Frédéric; Blouw, Johan; Blusk, Steven; Bocci, Valerio; Bondar, Alexander; Bondar, Nikolay; Bonivento, Walter; Borghi, Silvia; Borgia, Alessandra; Borsato, Martino; Bowcock, Themistocles; Bowen, Espen Eie; Bozzi, Concezio; Brambach, Tobias; Bressieux, Joël; Brett, David; Britsch, Markward; Britton, Thomas; Brodzicka, Jolanta; Brook, Nicholas; Brown, Henry; Bursche, Albert; Busetto, Giovanni; Buytaert, Jan; Cadeddu, Sandro; Calabrese, Roberto; Calvi, Marta; Calvo Gomez, Miriam; Campana, Pierluigi; Campora Perez, Daniel; Carbone, Angelo; Carboni, Giovanni; Cardinale, Roberta; Cardini, Alessandro; Carson, Laurence; Carvalho Akiba, Kazuyoshi; Casse, Gianluigi; Cassina, Lorenzo; Castillo Garcia, Lucia; Cattaneo, Marco; Cauet, Christophe; Cenci, Riccardo; Charles, Matthew; Charpentier, Philippe; Chefdeville, Maximilien; Chen, Shanzhen; Cheung, Shu-Faye; Chiapolini, Nicola; Chrzaszcz, Marcin; Ciba, Krzystof; Cid Vidal, Xabier; Ciezarek, Gregory; Clarke, Peter; Clemencic, Marco; Cliff, Harry; Closier, Joel; Coco, Victor; Cogan, Julien; Cogneras, Eric; Cojocariu, Lucian; Collins, Paula; Comerma-Montells, Albert; Contu, Andrea; Cook, Andrew; Coombes, Matthew; Coquereau, Samuel; Corti, Gloria; Corvo, Marco; Counts, Ian; Couturier, Benjamin; Cowan, Greig; Craik, Daniel Charles; Cruz Torres, Melissa Maria; Cunliffe, Samuel; Currie, Robert; D'Ambrosio, Carmelo; Dalseno, Jeremy; David, Pascal; David, Pieter; Davis, Adam; De Bruyn, Kristof; De Capua, Stefano; De Cian, Michel; De Miranda, Jussara; De Paula, Leandro; De Silva, Weeraddana; De Simone, Patrizia; Decamp, Daniel; Deckenhoff, Mirko; Del Buono, Luigi; Déléage, Nicolas; Derkach, Denis; Deschamps, Olivier; Dettori, Francesco; Di Canto, Angelo; Dijkstra, Hans; Donleavy, Stephanie; Dordei, Francesca; Dorigo, Mirco; Dosil Suárez, Alvaro; Dossett, David; Dovbnya, Anatoliy; Dreimanis, Karlis; Dujany, Giulio; Dupertuis, Frederic; Durante, Paolo; Dzhelyadin, Rustem; Dziurda, Agnieszka; Dzyuba, Alexey; Easo, Sajan; Egorychev, Victor; Eidelman, Semen; Eisenhardt, Stephan; Eitschberger, Ulrich; Ekelhof, Robert; Eklund, Lars; El Rifai, Ibrahim; Elsasser, Christian; Ely, Scott; Esen, Sevda; Evans, Hannah Mary; Evans, Timothy; Falabella, Antonio; Färber, Christian; Farinelli, Chiara; Farley, Nathanael; Farry, Stephen; Fay, Robert; Ferguson, Dianne; Fernandez Albor, Victor; Ferreira Rodrigues, Fernando; Ferro-Luzzi, Massimiliano; Filippov, Sergey; Fiore, Marco; Fiorini, Massimiliano; Firlej, Miroslaw; Fitzpatrick, Conor; Fiutowski, Tomasz; Fol, Philip; Fontana, Marianna; Fontanelli, Flavio; Forty, Roger; Francisco, Oscar; Frank, Markus; Frei, Christoph; Frosini, Maddalena; Fu, Jinlin; Furfaro, Emiliano; Gallas Torreira, Abraham; Galli, Domenico; Gallorini, Stefano; Gambetta, Silvia; Gandelman, Miriam; Gandini, Paolo; Gao, Yuanning; García Pardiñas, Julián; Garofoli, Justin; Garra Tico, Jordi; Garrido, Lluis; Gaspar, Clara; Gauld, Rhorry; Gavardi, Laura; Gavrilov, Gennadii; Geraci, Angelo; Gersabeck, Evelina; Gersabeck, Marco; Gershon, Timothy; Ghez, Philippe; Gianelle, Alessio; Gianì, Sebastiana; Gibson, Valerie; Giubega, Lavinia-Helena; Gligorov, Vladimir; Göbel, Carla; Golubkov, Dmitry; Golutvin, Andrey; Gomes, Alvaro; Gotti, Claudio; Grabalosa Gándara, Marc; Graciani Diaz, Ricardo; Granado Cardoso, Luis Alberto; Graugés, Eugeni; Graziani, Giacomo; Grecu, Alexandru; Greening, Edward; Gregson, Sam; Griffith, Peter; Grillo, Lucia; Grünberg, Oliver; Gui, Bin; Gushchin, Evgeny; Guz, Yury; Gys, Thierry; Hadjivasiliou, Christos; Haefeli, Guido; Haen, Christophe; Haines, Susan; Hall, Samuel; Hamilton, Brian; Hampson, Thomas; Han, Xiaoxue; Hansmann-Menzemer, Stephanie; Harnew, Neville; Harnew, Samuel; Harrison, Jonathan; He, Jibo; Head, Timothy; Heijne, Veerle; Hennessy, Karol; Henrard, Pierre; Henry, Louis; Hernando Morata, Jose Angel; van Herwijnen, Eric; Heß, Miriam; Hicheur, Adlène; Hill, Donal; Hoballah, Mostafa; Hombach, Christoph; Hulsbergen, Wouter; Hunt, Philip; Hussain, Nazim; Hutchcroft, David; Hynds, Daniel; Idzik, Marek; Ilten, Philip; Jacobsson, Richard; Jaeger, Andreas; Jalocha, Pawel; Jans, Eddy; Jaton, Pierre; Jawahery, Abolhassan; Jing, Fanfan; John, Malcolm; Johnson, Daniel; Jones, Christopher; Joram, Christian; Jost, Beat; Jurik, Nathan; Kaballo, Michael; Kandybei, Sergii; Kanso, Walaa; Karacson, Matthias; Karbach, Moritz; Karodia, Sarah; Kelsey, Matthew; Kenyon, Ian; Ketel, Tjeerd; Khanji, Basem; Khurewathanakul, Chitsanu; Klaver, Suzanne; Klimaszewski, Konrad; Kochebina, Olga; Kolpin, Michael; Komarov, Ilya; Koopman, Rose; Koppenburg, Patrick; Korolev, Mikhail; Kozlinskiy, Alexandr; Kravchuk, Leonid; Kreplin, Katharina; Kreps, Michal; Krocker, Georg; Krokovny, Pavel; Kruse, Florian; Kucewicz, Wojciech; Kucharczyk, Marcin; Kudryavtsev, Vasily; Kurek, Krzysztof; Kvaratskheliya, Tengiz; La Thi, Viet Nga; Lacarrere, Daniel; Lafferty, George; Lai, Adriano; Lambert, Dean; Lambert, Robert W; Lanfranchi, Gaia; Langenbruch, Christoph; Langhans, Benedikt; Latham, Thomas; Lazzeroni, Cristina; Le Gac, Renaud; van Leerdam, Jeroen; Lees, Jean-Pierre; Lefèvre, Regis; Leflat, Alexander; Lefrançois, Jacques; Leo, Sabato; Leroy, Olivier; Lesiak, Tadeusz; Leverington, Blake; Li, Yiming; Likhomanenko, Tatiana; Liles, Myfanwy; Lindner, Rolf; Linn, Christian; Lionetto, Federica; Liu, Bo; Lohn, Stefan; Longstaff, Iain; Lopes, Jose; Lopez-March, Neus; Lowdon, Peter; Lu, Haiting; Lucchesi, Donatella; Luo, Haofei; Lupato, Anna; Luppi, Eleonora; Lupton, Oliver; Machefert, Frederic; Machikhiliyan, Irina V; Maciuc, Florin; Maev, Oleg; Malde, Sneha; Malinin, Alexander; Manca, Giulia; Mancinelli, Giampiero; Mapelli, Alessandro; Maratas, Jan; Marchand, Jean François; Marconi, Umberto; Marin Benito, Carla; Marino, Pietro; Märki, Raphael; Marks, Jörg; Martellotti, Giuseppe; Martens, Aurelien; Martín Sánchez, Alexandra; Martinelli, Maurizio; Martinez Santos, Diego; Martinez Vidal, Fernando; Martins Tostes, Danielle; Massafferri, André; Matev, Rosen; Mathe, Zoltan; Matteuzzi, Clara; Mazurov, Alexander; McCann, Michael; McCarthy, James; McNab, Andrew; McNulty, Ronan; McSkelly, Ben; Meadows, Brian; Meier, Frank; Meissner, Marco; Merk, Marcel; Milanes, Diego Alejandro; Minard, Marie-Noelle; Moggi, Niccolò; Molina Rodriguez, Josue; Monteil, Stephane; Morandin, Mauro; Morawski, Piotr; Mordà, Alessandro; Morello, Michael Joseph; Moron, Jakub; Morris, Adam Benjamin; Mountain, Raymond; Muheim, Franz; Müller, Katharina; Mussini, Manuel; Muster, Bastien; Naik, Paras; Nakada, Tatsuya; Nandakumar, Raja; Nasteva, Irina; Needham, Matthew; Neri, Nicola; Neubert, Sebastian; Neufeld, Niko; Neuner, Max; Nguyen, Anh Duc; Nguyen, Thi-Dung; Nguyen-Mau, Chung; Nicol, Michelle; Niess, Valentin; Niet, Ramon; Nikitin, Nikolay; Nikodem, Thomas; Novoselov, Alexey; O'Hanlon, Daniel Patrick; Oblakowska-Mucha, Agnieszka; Obraztsov, Vladimir; Oggero, Serena; Ogilvy, Stephen; Okhrimenko, Oleksandr; Oldeman, Rudolf; Onderwater, Gerco; Orlandea, Marius; Otalora Goicochea, Juan Martin; Owen, Patrick; Oyanguren, Maria Arantza; Pal, Bilas Kanti; Palano, Antimo; Palombo, Fernando; Palutan, Matteo; Panman, Jacob; Papanestis, Antonios; Pappagallo, Marco; Pappalardo, Luciano; Parkes, Christopher; Parkinson, Christopher John; Passaleva, Giovanni; Patel, Girish; Patel, Mitesh; Patrignani, Claudia; Pazos Alvarez, Antonio; Pearce, Alex; Pellegrino, Antonio; Pepe Altarelli, Monica; Perazzini, Stefano; Perez Trigo, Eliseo; Perret, Pascal; Perrin-Terrin, Mathieu; Pescatore, Luca; Pesen, Erhan; Petridis, Konstantin; Petrolini, Alessandro; Picatoste Olloqui, Eduardo; Pietrzyk, Boleslaw; Pilař, Tomas; Pinci, Davide; Pistone, Alessandro; Playfer, Stephen; Plo Casasus, Maximo; Polci, Francesco; Poluektov, Anton; Polycarpo, Erica; Popov, Alexander; Popov, Dmitry; Popovici, Bogdan; Potterat, Cédric; Price, Eugenia; Price, Joseph David; Prisciandaro, Jessica; Pritchard, Adrian; Prouve, Claire; Pugatch, Valery; Puig Navarro, Albert; Punzi, Giovanni; Qian, Wenbin; Rachwal, Bartolomiej; Rademacker, Jonas; Rakotomiaramanana, Barinjaka; Rama, Matteo; Rangel, Murilo; Raniuk, Iurii; Rauschmayr, Nathalie; Raven, Gerhard; Redi, Federico; Reichert, Stefanie; Reid, Matthew; dos Reis, Alberto; Ricciardi, Stefania; Richards, Sophie; Rihl, Mariana; Rinnert, Kurt; Rives Molina, Vincente; Robbe, Patrick; Rodrigues, Ana Barbara; Rodrigues, Eduardo; Rodriguez Perez, Pablo; Roiser, Stefan; Romanovsky, Vladimir; Romero Vidal, Antonio; Rotondo, Marcello; Rouvinet, Julien; Ruf, Thomas; Ruiz, Hugo; Ruiz Valls, Pablo; Saborido Silva, Juan Jose; Sagidova, Naylya; Sail, Paul; Saitta, Biagio; Salustino Guimaraes, Valdir; Sanchez Mayordomo, Carlos; Sanmartin Sedes, Brais; Santacesaria, Roberta; Santamarina Rios, Cibran; Santovetti, Emanuele; Sarti, Alessio; Satriano, Celestina; Satta, Alessia; Saunders, Daniel Martin; Savrie, Mauro; Savrina, Darya; Schiller, Manuel; Schindler, Heinrich; Schlupp, Maximilian; Schmelling, Michael; Schmidt, Burkhard; Schneider, Olivier; Schopper, Andreas; Schune, Marie Helene; Schwemmer, Rainer; Sciascia, Barbara; Sciubba, Adalberto; Seco, Marcos; Semennikov, Alexander; Sepp, Indrek; Serra, Nicola; Serrano, Justine; Sestini, Lorenzo; Seyfert, Paul; Shapkin, Mikhail; Shapoval, Illya; Shcheglov, Yury; Shears, Tara; Shekhtman, Lev; Shevchenko, Vladimir; Shires, Alexander; Silva Coutinho, Rafael; Simi, Gabriele; Sirendi, Marek; Skidmore, Nicola; Skwarnicki, Tomasz; Smith, Anthony; Smith, Edmund; Smith, Eluned; Smith, Jackson; Smith, Mark; Snoek, Hella; Sokoloff, Michael; Soler, Paul; Soomro, Fatima; Souza, Daniel; Souza De Paula, Bruno; Spaan, Bernhard; Sparkes, Ailsa; Spradlin, Patrick; Sridharan, Srikanth; Stagni, Federico; Stahl, Marian; Stahl, Sascha; Steinkamp, Olaf; Stenyakin, Oleg; Stevenson, Scott; Stoica, Sabin; Stone, Sheldon; Storaci, Barbara; Stracka, Simone; Straticiuc, Mihai; Straumann, Ulrich; Stroili, Roberto; Subbiah, Vijay Kartik; Sun, Liang; Sutcliffe, William; Swientek, Krzysztof; Swientek, Stefan; Syropoulos, Vasileios; Szczekowski, Marek; Szczypka, Paul; Szilard, Daniela; Szumlak, Tomasz; T'Jampens, Stephane; Teklishyn, Maksym; Tellarini, Giulia; Teubert, Frederic; Thomas, Christopher; Thomas, Eric; van Tilburg, Jeroen; Tisserand, Vincent; Tobin, Mark; Tolk, Siim; Tomassetti, Luca; Topp-Joergensen, Stig; Torr, Nicholas; Tournefier, Edwige; Tourneur, Stephane; Tran, Minh Tâm; Tresch, Marco; Tsaregorodtsev, Andrei; Tsopelas, Panagiotis; Tuning, Niels; Ubeda Garcia, Mario; Ukleja, Artur; Ustyuzhanin, Andrey; Uwer, Ulrich; Vacca, Claudia; Vagnoni, Vincenzo; Valenti, Giovanni; Vallier, Alexis; Vazquez Gomez, Ricardo; Vazquez Regueiro, Pablo; Vázquez Sierra, Carlos; Vecchi, Stefania; Velthuis, Jaap; Veltri, Michele; Veneziano, Giovanni; Vesterinen, Mika; Viaud, Benoit; Vieira, Daniel; Vieites Diaz, Maria; Vilasis-Cardona, Xavier; Vollhardt, Achim; Volyanskyy, Dmytro; Voong, David; Vorobyev, Alexey; Vorobyev, Vitaly; Voß, Christian; Voss, Helge; de Vries, Jacco; Waldi, Roland; Wallace, Charlotte; Wallace, Ronan; Walsh, John; Wandernoth, Sebastian; Wang, Jianchun; Ward, David; Watson, Nigel; Websdale, David; Whitehead, Mark; Wicht, Jean; Wiedner, Dirk; Wilkinson, Guy; Williams, Matthew; Williams, Mike; Wilschut, Hans; Wilson, Fergus; Wimberley, Jack; Wishahi, Julian; Wislicki, Wojciech; Witek, Mariusz; Wormser, Guy; Wotton, Stephen; Wright, Simon; Wyllie, Kenneth; Xie, Yuehong; Xing, Zhou; Xu, Zhirui; Yang, Zhenwei; Yuan, Xuhao; Yushchenko, Oleg; Zangoli, Maria; Zavertyaev, Mikhail; Zhang, Liming; Zhang, Wen Chao; Zhang, Yanxi; Zhelezov, Alexey; Zhokhov, Anatoly; Zhong, Liang; Zvyagin, Alexander

    2015-01-01

    Using the latest LHCb measurements of time-dependent $C\\!P$ violation in the $B^0_s \\to K^+K^-$ decay, a U-spin relation between the decay amplitudes of $B^0_s \\to K^+K^-$ and $B^0\\to \\pi^+\\pi^-$ decay processes allows constraints to be placed on the angle $\\gamma$ of the unitarity triangle and on the $B^0_s$ mixing phase $-2\\beta_s$. Results from an extended approach, which uses additional inputs on $B^0\\to \\pi^0\\pi^0$ and $B^+\\to \\pi^+\\pi^0$ decays from other experiments and exploits isospin symmetry, are also presented. The dependence of the results on the maximum allowed amount of U-spin breaking is studied. At 68% probability, the value $\\gamma = \\left( 63.5^{\\,+\\, 7.2}_{\\,-\\,6.7} \\right)^\\circ~\\mathrm{modulo}~180^\\circ$ is determined. In an alternative analysis, the value $-2\\beta_s = -0.12 ^{\\,+\\,0.14}_{\\,-\\,0.16}\\,\\,\\mathrm{rad}$ is found. In both measurements, the uncertainties due to U-spin breaking effects up to 50% are included.

  19. Three-dimensional density field determination by external stationary detectors and gamma sources using selective scattering

    International Nuclear Information System (INIS)

    Kondic, N.; Jacobs, A.; Ebert, D.

    1983-01-01

    In many fields one needs to know the spatial density distribution; two-phase systems are of particular importance. In particular, gas-liquid mixtures play a role in power generation, chemistry, bio-medicine etc. An intrusion into the measured system is frequently undesired or not permitted. Therefore, external, non-invasive instrumentation has definite advantages. Photon-energy discrimination methods, measuring scattered fluxes, can employ stationary equipment; they need partial collimation or only protective shielding. The results are achieved with a higher information/irradiation ratio than is the case with transmission methods. The utilization a mesh of isogonic lines (each of them being characterised by its particular scattering angle) has several advantages when compared with the mesh of straight lines (''pencil beams'') used in tomography. The ultimate experimental arrangement employing Compton scattering has fan/fan beam geometry, i.e., wide angle emitting and receiving of gammas. The direct result of the measurement is a ''scattergram'', i.e., countrate versus scattered energy spectrum. Besides representing the ''signature'' of a two- or three-dimensional density distribution, it also enables the reconstruction of local density values. The report outlines the necessary analysis and presents experimental proof of principle

  20. Determination of activity by gamma spectrometry of radionuclides present in drums of residues generated in nuclear centrals

    International Nuclear Information System (INIS)

    Aguiar, J.C.; Fernandez, J.

    2006-01-01

    The generation of radioactive residuals in nuclear centrals as CNA I (Atucha I Nuclear Central) and CNE (Embalse Nuclear Central) makes that the measurement of those radionuclides has been a previous stage to the waste management. A method used in those nuclear centrals it is the gamma spectrometry with HPGe detectors, previous to the immobilization of the residual in a cemented matrix, with this the contact with the external agents and its possible dispersion to the atmosphere in the short term is avoided. The ARN (Nuclear Regulatory Authority) of Argentina it carries out periodically intercomparisons and evaluations of the measurement and procedures systems used in the nuclear power stations for the correct measurement and determination of activity of radioactive residuals by gamma spectrometry. In this work an independent method of measurement is exposed to the nuclear power stations. To determine the activity of the residuals by gamma spectrometry deposited in drums, it is required of the precise knowledge of the efficiency curve for such geometry and matrix. Due to the RNA doesn't have a pattern of these characteristics, a mathematical model has been used to obtain this efficiency curve. For it, it is necessary to determine previously: 1) the geometric efficiency or solid angle sustained by the source-detector system (drum-detector) applying a mathematical model described in this work. 2) To estimate the auto-attenuation factor that present the photons in the cemented matrix, these calculations are carried out with a simple equation and its are verified with the Micro Shield 6.10 program. The container commonly used by these nuclear power stations its are drums for 220 liters constructed with SAE 1010 steel and with a thickness of 0.127 cm, with an approximate weight 7.73 Kg., internal diameter of 57.1 cm, and height: 87 cm. The results obtained until the moment register a discrepancy from 5 to 10% with relationship to the measurements carried out by the

  1. Theoretical determination of gamma spectrometry systems efficiency based on probability functions. Application to self-attenuation correction factors

    Energy Technology Data Exchange (ETDEWEB)

    Barrera, Manuel, E-mail: manuel.barrera@uca.es [Escuela Superior de Ingeniería, University of Cadiz, Avda, Universidad de Cadiz 10, 11519 Puerto Real, Cadiz (Spain); Suarez-Llorens, Alfonso [Facultad de Ciencias, University of Cadiz, Avda, Rep. Saharaui s/n, 11510 Puerto Real, Cadiz (Spain); Casas-Ruiz, Melquiades; Alonso, José J.; Vidal, Juan [CEIMAR, University of Cadiz, Avda, Rep. Saharaui s/n, 11510 Puerto Real, Cádiz (Spain)

    2017-05-11

    A generic theoretical methodology for the calculation of the efficiency of gamma spectrometry systems is introduced in this work. The procedure is valid for any type of source and detector and can be applied to determine the full energy peak and the total efficiency of any source-detector system. The methodology is based on the idea of underlying probability of detection, which describes the physical model for the detection of the gamma radiation at the particular studied situation. This probability depends explicitly on the direction of the gamma radiation, allowing the use of this dependence the development of more realistic and complex models than the traditional models based on the point source integration. The probability function that has to be employed in practice must reproduce the relevant characteristics of the detection process occurring at the particular studied situation. Once the probability is defined, the efficiency calculations can be performed in general by using numerical methods. Monte Carlo integration procedure is especially useful to perform the calculations when complex probability functions are used. The methodology can be used for the direct determination of the efficiency and also for the calculation of corrections that require this determination of the efficiency, as it is the case of coincidence summing, geometric or self-attenuation corrections. In particular, we have applied the procedure to obtain some of the classical self-attenuation correction factors usually employed to correct for the sample attenuation of cylindrical geometry sources. The methodology clarifies the theoretical basis and approximations associated to each factor, by making explicit the probability which is generally hidden and implicit to each model. It has been shown that most of these self-attenuation correction factors can be derived by using a common underlying probability, having this probability a growing level of complexity as it reproduces more precisely

  2. Determination of Non-Transferrin Bound Iron, Transferrin Bound Iron, Drug Bound Iron and Total Iron in Serum in a Rats after IV Administration of Sodium Ferric Gluconate Complex by Simple Ultrafiltration Inductively Coupled Plasma Mass Spectrometric Detection

    Directory of Open Access Journals (Sweden)

    Murali K. Matta

    2018-02-01

    Full Text Available A rapid, sensitive and specific ultrafiltration inductively-coupled plasma mass spectrometry method was developed and validated for the quantification of non-transferrin bound iron (NTBI, transferrin bound iron (TBI, drug bound iron (DI and total iron (TI in the same rat serum sample after intravenous (IV administration of iron gluconate nanoparticles in sucrose solution (Ferrlecit®. Ultrafiltration with a 30 kDa molecular cut-off filter was used for sample cleanup. Different elution solvents were used to separate each form of iron from sample serum. Isolated fractions were subjected to inductively-coupled mass spectrometric analysis after microwave digestion in 4% nitric acid. The reproducibility of the method was evaluated by precision and accuracy. The calibration curve demonstrated linearity from 5–500 ng/mL with a regression (r2 of more than 0.998. This method was effectively implemented to quantify rat pharmacokinetic study samples after intravenous administration of Ferrlecit®. The method was successfully applied to a pharmacokinetic (PK study of Ferrlecit in rats. The colloidal iron followed first order kinetics with half-life of 2.2 h and reached background or pre-dose levels after 12 h post-dosing. The drug shown a clearance of 0.31 mL/min/kg and volume of distribution of 0.05 L/kg. 19.4 ± 2.4 mL/h/kg.

  3. Determination of porosity in supports for ceramic membranes of titanium dioxide by gamma spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Siciliano, Umberto C.C.S.; Oliveira, Elizabeth E.M.; Brandão, Luís E.B.; Carvalho, Paulo V.R., E-mail: ucsiciliano@gmail.com, E-mail: eemo@ien.gov.br, E-mail: brandao@ien.gov.br, E-mail: paulov@ien.gov.br [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

    2017-07-01

    Membrane separation processes (MSP) have been widely used to fractionate, concentrate and purity solutions, such as: food industry, pharmaceutical, water desalination and for treatment of the radioactive liquid waste in the nuclear industry. The MSP are more economical than traditional methods because most of them are athermic. Increased membrane application has led to the expansion of the manufacturing technology knowledge base, resulting in membranes with high permeability, improved selectivity and long-term stability. The demand for high operating temperatures and chemical resistance have stimulated the development of inorganic structures, mainly porous ceramics. The materials most used to obtain ceramic membranes are oxides like Ab0{sub 3}, Si0{sub 2}, Zr0{sub 2} and Ti0{sub 2} or combination of these. Despite the favorable characteristics, ceramic membranes has not been applied extensively, mainly due to the difficulty of obtaining porous structures without cracks and with adequate pore size. The objective of this work is obtain a support of titanium oxide using potato starch as a pore former. The titanium oxide used is commercial, with average particle size of 0.13 μm. Three suspensions were prepared containing 0,5 and 10 % of the potato starch and the drying in spray dryer, obtaining a homogeneous and granulated powder, with flow ability suitable for compaction. The supports were uniaxial pressing with l.5 kgf.cm{sup -2} and sintering at temperatures of 1050, 1100 and 1150 °C for 1h in oven resistance. The results showed that the porosity obtained by gamma ray transmission method was approximately 50%. This value is within range for applications as membrane support. (author)

  4. Determination of gamma radiation dose as a post-harvest treatment in mangos infested with the South American fruit fly

    International Nuclear Information System (INIS)

    Alama, D.

    1999-01-01

    Efforts are being made to determine a gamma radiation dose for mortality of third-instar larvae of Anastrepha fraterculus which infest mangos of the Haden variety of 400 g weight. Four radiation treatments were tested: 0.4 kGy, 0.6 kGy, 0.8 kGy and 1.0 kGy. Using as a criterium for mortality the interruption of the biological cycle between larva and pupa, the following results were achieved: 49.61%, 63.33%, 74.86% and 90.72%. The percentages obtained have been corrected using the Abbot formula. When the criterium was based on no adult emergence, 100% mortality was achieved for the four treatments. (author)

  5. Simultaneous determination of soil density and moisture by gamma ray attenuation from Cs137 and Am241

    International Nuclear Information System (INIS)

    Barros Ferraz, E.S. de.

    1974-09-01

    The method of simultaneous bulk density and soil moisture determination by attenuation of 241 Am and 137 Cs gamma-radiation is introduced and studied with details. Theoretical considerations are made about the attenuation process in the absorbers, the form of solving the problem of two unknowns; the sensitivity of the method; the influences of the resolution time of the electronic counting equipment, and of the compton scattering in the sample. From the methodological point of view studies are made about the influence of the geometry, adjustment of counting system, choice of radiation sources, attenuation coeficients and the manner of obtaining reliable measurements. It is also presented some applications of the method, its use in soil-water movement studies, in soil profile compaction studies, and specially in swelling soils

  6. Optimum method to determine gamma activity in 200 liter drums. In-toto measurement or extracting a sample

    International Nuclear Information System (INIS)

    Bronson, Frazier

    2008-01-01

    In the process of decommissioning contaminated facilities, and in the conduct of normal operations involving radioactive material, it is frequently required to measure radioactivity in large containers such as 200 liter drums. For solid material, it is quite unusual for the radioactivity to be homogeneously distributed throughout the container. One way to derive the concentration of radioactivity within the container is to extract a sample for subsequent measurement in the laboratory. Another way is to use gamma spectroscopy and assay the entire container, or in-toto measurement. This paper examines the process of determining the best way to estimate the activity within the container, and gives quantitative estimates of measurement uncertainty for various conditions of radioactivity contained within 200 liter drums. When the contents of the container are not homogeneous, the sampling uncertainty is likely to be larger than the in-toto measurement uncertainty. (author)

  7. Determination of a Thorium Content in Soil Samples by Means of Gamma-Activation Analysis and X-Ray Spectrometry

    CERN Document Server

    Maslov, O D; Gustova, M V; Dmitriev, S N

    2003-01-01

    A highly sensitive method based on the reaction ^{232}Th(\\gamma, n)^{231}Th (T_{1/2} = 25.5 h) is developed for determining thorium in soil and environmental samples with a thorium content at a level of 3x10^{-7} g/g. Samples were irradiated for 4 hours with a maximum photon energy of 24.5 MeV at a compact electron accelerator - the MT-25 microtron of FLNR, JINR. The average electron current was about 15 {\\mu}A. The irradiated samples were tested using an X-ray spectrometer with a Si(Li) detector and a resolution of 200 eV (Fe_{K\\alpha} - 6.4 keV).

  8. Quantitative MALDI tandem mass spectrometric imaging of cocaine from brain tissue with a deuterated internal standard.

    NARCIS (Netherlands)

    Pirman, D.A.; Reich, R.F.; Kiss, A.; Heeren, R.M.A.; Yost, R.A.

    2013-01-01

    Mass spectrometric imaging (MSI) is an analytical technique used to determine the distribution of individual analytes within a given sample. A wide array of analytes and samples can be investigated by MSI, including drug distribution in rats, lipid analysis from brain tissue, protein differentiation

  9. Comparative determination of uranium in rock phosphates and columbite by ICP-OES, alpha and gamma spectrometry

    International Nuclear Information System (INIS)

    Singhal, R.K.; Sharma, P.K.; Bassan, M.K.T.; Basu, H.; Reddy, A.V.R.

    2011-01-01

    During this work selective separation of uranium from rock phosphate and columbite mineral was done before its quantitative estimation by using Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES). Uranium from the rock phosphate and columbite was extracted by sodium peroxide fusion followed by leaching in 2 M HNO 3 . To avoid spectral interference in the estimation of uranium by ICP-OES, the selective separation of uranium from the leachate was carried out by using two different extractants, 30% Tributyl Phosphates (TBP) in CCl 4 and a equi-volume mixture of Di(2-ethylhexyl) phosphoric acid (D2EHPA) and TBP in petrofin. Uranium was stripped from the organic phase by using 1 M ammonium carbonate solution. Determination of uranium by ICP-OES was done after dissolving the residue left after evaporation of ammonium carbonate solution in 4% HNO 3 . The concentration of the uranium observed in the rock phosphates samples was 40-200 μg g -1 whereas in columbite samples the concentration range was 100-600 μg g -1 . Uranium concentration evaluated by ICP-OES was complimented by gamma and alpha spectrometry. Concentration of uranium evaluated by gamma spectrometry in case of rock phosphate and columbite was in close agreement with the uranium content obtained by ICP-OES. Uranium determination by alpha spectrometry showed only minor deviation (1-2%) from the results obtained by ICP-OES in case of rock phosphates whereas in case of columbites results are off by 20-30%. (author)

  10. Determination of the natural radioactivity levels in north west of Dukhan, Qatar using high-resolution gamma-ray spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Al-Sulaiti, Huda, E-mail: h.al-sulaiti@surrey.ac.uk [Centre for Nuclear and Radiation Physics, Department of Physics, University of Surrey, Guildford GU2 7XH (United Kingdom); Radiation Protection and Chemicals Department, Ministry of Environment, P.O. Box 7634, Doha (Qatar); Nasir, Tabassum [Centre for Nuclear and Radiation Physics, Department of Physics, University of Surrey, Guildford GU2 7XH (United Kingdom); Department of Physics, Gomal University, D.I. Khan (Pakistan); Al Mugren, K.S. [Centre for Nuclear and Radiation Physics, Department of Physics, University of Surrey, Guildford GU2 7XH (United Kingdom); Physics Department, Faculty of Sciences, Princess Nora Bint Abdul Rahman University, Riyadh (Saudi Arabia); Alkhomashi, N. [King Abdulaziz City of Science and Technology (KACST), P.O. Box 6086, Riyadh 11442 (Saudi Arabia); Al-Dahan, N. [Centre for Nuclear and Radiation Physics, Department of Physics, University of Surrey, Guildford GU2 7XH (United Kingdom); Department of Physics, College of Science, University of Kerbala, Kerbala (Iraq); Al-Dosari, M. [Radiation Protection and Chemicals Department, Ministry of Environment, P.O. Box 7634, Doha (Qatar); Bradley, D.A. [Centre for Nuclear and Radiation Physics, Department of Physics, University of Surrey, Guildford GU2 7XH (United Kingdom); Bukhari, S. [Information Systems Management Department, Ministry of Environment, P.O. Box 7634, Doha (Qatar); Matthews, M. [Centre of Environmental Health Engineering, Department of Civil Engineering, University of Surrey, Guildford GU2 7XH (United Kingdom); Regan, P.H. [Centre for Nuclear and Radiation Physics, Department of Physics, University of Surrey, Guildford GU2 7XH (United Kingdom); Santawamaitre, T. [Radiation Protection and Chemicals Department, Ministry of Environment, P.O. Box 7634, Doha (Qatar); Malain, D.; Habib, A. [Centre for Nuclear and Radiation Physics, Department of Physics, University of Surrey, Guildford GU2 7XH (United Kingdom)

    2012-07-15

    This study is aimed at the determination of the activity concentrations of naturally occuring and technologically enhanced levels of radiation in 34 representative soil samples that have been collected from an inshore oil field area which was found to have, in a previous study, the highest observed value of {sup 226}Ra concentration among 129 soil samples. The activity concentrations of {sup 238}U and {sup 226}Ra have been inferred from gamma-ray transitions associated with their decay progenies and measured using a hyper-pure germanium detector. Details of the sample preparation and the gamma-ray spectroscopic analysis techniques are presented, together with the values of the activity concentrations associated with the naturally occuring radionuclide chains for all the samples collected from NW Dukhan. Discrete-line, gamma-ray energy transitions from spectral lines ranging in energy from {approx}100 keV up to 2.6 MeV have been associated with characteristic decays of the various decay products within the {sup 235.8}U and {sup 232}Th radioactive decay chains. These data have been analyzed, under the assumption of secular equilibrium for the U and Th decay chains. Details of the sample preparation and the gamma-ray spectroscopic analysis techniques are presented. The weighted mean value of the activity concentrations of {sup 226}Ra in one of the samples was found to be around a factor of 2 higher than the values obtained in the previous study and approximately a factor of 10 higher than the accepted worldwide average value of 35 Bq/kg. The weighted mean values of the activity concentrations of {sup 232}Th and {sup 40}K were also deduced and found to be within the worldwide average values of 30 and 400 Bq/kg, respectively. Our previous study reported a value of 201.9{+-}1.5{sub Stat.}{+-}13{sub Syst.} Bq/kg for {sup 226}Ra in one sample and further investigation in the current work determined a measured value for {sup 226}Ra of 342.00{+-}1.9{sub Stat.}{+-}25{sub Syst

  11. One procedure for determination of the neutron flux in the nuclear reactor fuel

    International Nuclear Information System (INIS)

    Bulovic, V.; Krtil, J.; Maksimovic, Z.; Martinc, R.

    1979-09-01

    Possibility of determination of the neutron flux in the fuel of a heavy water reactor has been examined. In determination of the flux an iterative procedure was used to compare calculated and measured contents of several fission products. The former contents were determined by calculation of the burning process balance and the latter by non-destructive gamma-spectrometric analysis of fuel. The obtained results prove the possibility of such determination of not only the average value of the flux but also of the change of its intensity during utilization of fuel (author) [sr

  12. Novel atomic absorption spectrometric and rapid spectrophotometric methods for the quantitation of paracetamol in saliva: application to pharmacokinetic studies.

    Science.gov (United States)

    Issa, M M; Nejem, R M; El-Abadla, N S; Al-Kholy, M; Saleh, Akila A

    2008-01-01

    A novel atomic absorption spectrometric method and two highly sensitive spectrophotometric methods were developed for the determination of paracetamol. These techniques based on the oxidation of paracetamol by iron (III) (method I); oxidation of p-aminophenol after the hydrolysis of paracetamol (method II). Iron (II) then reacts with potassium ferricyanide to form Prussian blue color with a maximum absorbance at 700 nm. The atomic absorption method was accomplished by extracting the excess iron (III) in method II and aspirates the aqueous layer into air-acetylene flame to measure the absorbance of iron (II) at 302.1 nm. The reactions have been spectrometrically evaluated to attain optimum experimental conditions. Linear responses were exhibited over the ranges 1.0-10, 0.2-2.0 and 0.1-1.0 mug/ml for method I, method II and atomic absorption spectrometric method, respectively. A high sensitivity is recorded for the proposed methods I and II and atomic absorption spectrometric method value indicate: 0.05, 0.022 and 0.012 mug/ml, respectively. The limit of quantitation of paracetamol by method II and atomic absorption spectrometric method were 0.20 and 0.10 mug/ml. Method II and the atomic absorption spectrometric method were applied to demonstrate a pharmacokinetic study by means of salivary samples in normal volunteers who received 1.0 g paracetamol. Intra and inter-day precision did not exceed 6.9%.

  13. Structure elucidation of metabolite x17299 by interpretation of mass spectrometric data.

    Science.gov (United States)

    Zhang, Qibo; Ford, Lisa A; Evans, Anne M; Toal, Douglas R

    2017-01-01

    A major bottleneck in metabolomic studies is metabolite identification from accurate mass spectrometric data. Metabolite x17299 was identified in plasma as an unknown in a metabolomic study using a compound-centric approach where the associated ion features of the compound were used to determine the true molecular mass. The aim of this work is to elucidate the chemical structure of x17299, a new compound by de novo interpretation of mass spectrometric data. An Orbitrap Elite mass spectrometer was used for acquisition of mass spectra up to MS 4 at high resolution. Synthetic standards of N,N,N -trimethyl-l-alanyl-l-proline betaine (l,l-TMAP), a diastereomer, and an enantiomer were chemically prepared. The planar structure of x17299 was successfully proposed by de novo mechanistic interpretation of mass spectrometric data without any laborious purification and nuclear magnetic resonance spectroscopic analysis. The proposed structure was verified by deuterium exchanged mass spectrometric analysis and confirmed by comparison to a synthetic standard. Relative configuration of x17299 was determined by direct chromatographic comparison to a pair of synthetic diastereomers. Absolute configuration was assigned after derivatization of x17299 with a chiral auxiliary group followed by its chromatographic comparison to a pair of synthetic standards. The chemical structure of metabolite x17299 was determined to be l,l-TMAP.

  14. Spectrometric aerial survey as a new tool for geological survey and mining prospecting

    International Nuclear Information System (INIS)

    Cambon, R.

    1997-01-01

    Airborne survey for radioactive minerals started around 1945. The limited sensitivity of the tools used, the difficulties found for the topographic and training effect corrections, made difficult the evaluation of the results. The technical progresses realized in the recent past years in electronic and computer sciences allowed to overcome these difficulties and gave to the method all its potentialities. With the aerial spectrometric survey, a new step was made, because this method can be used for other topics than radioactive prospection such as geological survey and mining prospection for metallic and industrial minerals. The spectrometric method is based on the possibility to measure photopeak energies (gamma radiation) emitted by radioactive minerals and discriminate between them those emitted by U238, TI 208 and K40 respectively daughter products of uranium, thorium and potassium. For airborne survey, one consider that measuring instruments will allow to pick-up 80% of the radioactive emission concerning the first 15 to 30 centimetres of ground (1 metre maximum). The use of this method for geological and mineral exploration is based on the assumption that different rock types or ore bearing rock types are composed of certain amounts of rock forming minerals which comprise specific quantities of radioactive elements such as potassium, uranium and thorium (cf: Gabelman 77). To be able to evaluate the results of the spectrometric survey it will be necessary to know roughly the behaviour of the different radioactive elements through a complete geological cycle. (author)

  15. Determination of Optimum Planar Imaging Parameters for Small Structures with Diameters Less Than the Resolution of the Gamma Camera

    Directory of Open Access Journals (Sweden)

    Mpumelelo Nyathi

    2017-12-01

    Full Text Available Introduction: The limited spatial resolution of the gamma camera hinders the absolute quantification of planar images of small structures. The imaged structures are affected by partial volume effects (PVEs, which can spread activity and lead to underestimation of the regional distribution.  The use of optimum planar parameters reduces the impact of the limited spatial resolution of the gamma camera and the statistical noise inherent to low photon count, thus improving quantification. In this study, we aimed to determine the optimum planar imaging parameters for small structures. Materials and Methods: A thyroid protocol was used to acquire planar images of the spheres A, B, and C (16 mm, 12 mm, and 11 mm in diameter, respectively whilst filled with a targeted activity concentration of technetium-99m. One sphere was mounted at the centre of the Jaszczak Phantom and the other two adjacent to its walls using capillary stems fitted on the spheres. The phantom was filled with distilled water. The targeted activity concentrations used were 74 kBq/mL, 100 kBq/mL, 150 kBq/mL, and 300 kBq/mL. Images of the same count per pixel were acquired on 64  64, 128  128, 256  256, 512  512, and 1024  1024 pixels using a vertical detector mounted 5 cm above the phantom. All the images were quantified using ImageJ software, version 1.48a, Java 1.70_51 [64-bit]. Results: The optimum planar imaging parameters established were a matrix size of 128 128 pixels and technetium-99m solution of activity concentration of 300 kBq/ml. Conclusion: The use of optimal imaging parameters reduces the impact of PVEs, leading to improved quantitative accuracy.

  16. Comparison of analytical methods used to determine 235U, 238U and 210Pb from sediment samples by alpha, beta and gamma spectrometry

    International Nuclear Information System (INIS)

    Vesterbacka, P.; Klemola, S.; Salahel-Din, K.

    2009-01-01

    An intercomparison of the methodology (alpha, beta and gamma spectrometry) used for 238 U, 235 U and 210 Pb determination was carried out based on 38 sediment samples. The activity range of the samples varied from 10-700 Bq/kg for 210 Pb, 1-35 Bq/kg for 235 U and 10-800 Bq/ kg for 238 U. Results obtained using the three methods were not statistically different at high activity levels, but agreement between the results decreased at lower sample activity levels. For 210 Pb, the smallest difference was found between alpha and gamma spectrometry. A good correlation between results from alpha and gamma spectrometry was observed over the whole activity range. In beta spectrometry, the results were slightly higher than those obtained by alpha or gamma spectrometry due to the impurity of 228 Ra. In 238 U analysis, good correspondence was observed between 238 U determined by gamma and alpha spectrometry, particularly at higher 238 U activity concentrations over 100 Bq/kg. In 235 U analysis, attention needs to be paid to interference from 226 Ra and its reduction. (author)

  17. Assessment of measurement result uncertainty in determination of 210Pb with the focus on matrix composition effect in gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Iurian, A.R.; Pitois, A.; Kis-Benedek, G.; Migliori, A.; Padilla-Alvarez, R.; Ceccatelli, A.

    2016-01-01

    Reference materials were used to assess measurement result uncertainty in determination of 210 Pb by gamma-ray spectrometry, liquid scintillation counting, or indirectly by alpha-particle spectrometry, using its daughter 210 Po in radioactive equilibrium. Combined standard uncertainties of 210 Pb massic activities obtained by liquid scintillation counting are in the range 2–12%, depending on matrices and massic activity values. They are in the range 1–3% for the measurement of its daughter 210 Po using alpha-particle spectrometry. Three approaches (direct computation of counting efficiency and efficiency transfer approaches based on the computation and, respectively, experimental determination of the efficiency transfer factors) were applied for the evaluation of 210 Pb using gamma-ray spectrometry. Combined standard uncertainties of gamma-ray spectrometry results were found in the range 2–17%. The effect of matrix composition on self-attenuation was investigated and a detailed assessment of uncertainty components was performed. - Highlights: • Confirmed 210 Pb certified values by LSC and alpha-particle spectrometry ( 210 Po). • Assessed 210 Po measurement result uncertainty by alpha-particle spectrometry. • Matrix composition effect on gamma-ray spectrometry measurement result uncertainty. • Assessment of 210 Pb measurement result uncertainty by gamma-ray spectrometry. • Comparison of techniques and approaches: ‘fit-for-purpose’ considerations.

  18. Determination of gamma radiation dose for destruction of Salmonella spp. in chicken flesh

    International Nuclear Information System (INIS)

    Santos, Andreia Ferreira dos

    1997-01-01

    The aim of this study was to determinate: 1) the radio sensibility of Salmonella typhimurium ATCC 14028 in soy trypticase broth; 2) the radio sensibility of Salmonella typhimurium ATCC 14028 in chicken thigh and; 3) to recommend a radiation dose which can be non hazardous for human consumption

  19. Spectrometric characteristics of polystyrene scintillation films

    CERN Document Server

    Astvatsaturov, A R; Gavalyan, V B; Gavalyan, V G

    1999-01-01

    The spectrometric characteristics of five types of polystyrene scintillation films with thicknesses of 10, 30, 50 and 80 mu m and of analogous 250 mu m thick plates irradiated with sup 2 sup 3 sup 9 Pu, sup 2 sup 3 sup 8 Pu and sup 2 sup 2 sup 6 Ra sources of alpha-particles have been studied. The prospects of utilization of scintillation films as radiators for detection of heavy charged particles and measurement of their energy was experimentally shown.

  20. Quantifying the passive gamma signal from spent nuclear fuel in support of determining the plutonium content in spent nuclear fuel with nondestructive assay

    Energy Technology Data Exchange (ETDEWEB)

    Fensin, Michael L [Los Alamos National Laboratory; Tobin, Steven J [Los Alamos National Laboratory; Menlove, Howard O [Los Alamos National Laboratory; Swinhoe, Martyn T [Los Alamos National Laboratory

    2009-01-01

    The objective of safeguarding nuclear material is to deter diversions of significant quantities of nuclear materials by timely monitoring and detection. There are a variety of motivations for quantifying plutonium in spent fuel (SF), by means of nondestructive assay (NDA), in order to meet this goal. These motivations include the following: strengthening the capabilities of the International Atomic Energy Agencies ability to safeguard nuclear facilities, shipper/receiver difference, input accountability at reprocessing facilities and burnup credit at repositories. Many NDA techniques exist for measuring signatures from SF; however, no single NDA technique can, in isolation, quantify elemental plutonium in SF. A study has been undertaken to determine the best integrated combination of 13 NDA techniques for characterizing Pu mass in spent fuel. This paper focuses on the development of a passive gamma measurement system in support the spent fuel assay system. Gamma ray detection for fresh nuclear fuel focuses on gamma ray emissions that directly coincide with the actinides of interest to the assay. For example, the 186-keV gamma ray is generally used for {sup 235}U assay and the 384-keV complex is generally used for assaying plutonium. In spent nuclear fuel, these signatures cannot be detected as the Compton continuum created from the fission products dominates the signal in this energy range. For SF, the measured gamma signatures from key fission products ({sup 134}Cs, {sup 137}Cs, {sup 154}Eu) are used to ascertain burnup, cooling time, and fissile content information. In this paper the Monte Carlo modeling set-up for a passive gamma spent fuel assay system will be described. The set-up of the system includes a germanium detector and an ion chamber and will be used to gain passive gamma information that will be integrated into a system for determining Pu in SF. The passive gamma signal will be determined from a library of {approx} 100 assemblies that have been

  1. Gamma gamma technology group

    Indian Academy of Sciences (India)

    The gamma gamma community are concerned that in the rush to prepare for the e+e− machine, allowance is not being made for a future upgrade of the photon linear collider. References. [1] ECFA/DESY Photon Collider Working Group: B Badelek et al, TESLA Technical. Design Report, Part VI, Chapter 1: Photon collider at ...

  2. High-precision (p,t) reaction to determine Al-25(p,gamma)Si-26 reaction rates

    NARCIS (Netherlands)

    Matic, A.; van den Berg, A. M.; Harakeh, M. N.; Wörtche, H. J.; Berg, G. P. A.; Couder, M.; Goerres, J.; LeBlanc, P.; O'Brien, S.; Wiescher, M.; Fujita, K.; Hatanaka, K.; Sakemi, Y.; Shimizu, Y.; Tameshige, Y.; Tamii, A.; Yosoi, M.; Adachi, T.; Fujita, Y.; Shimbara, Y.; Fujita, H.; Wakasa, T.; Brown, B. A.; Schatz, H.

    2010-01-01

    Since the identification of ongoing Al-26 production in the universe, the reaction sequence Mg-24(p,gamma)Al-25(beta(+)nu)Mg-25(p,gamma)Al-26 has been studied intensively. At temperatures where the radiative capture on Al-25 (t(1/2) = 7.2 s) becomes faster than the beta(+) decay, the production of

  3. Zirconium and Yttrium (p, d) Surrogate Nuclear Reactions: Measurement and determination of gamma-ray probabilities: Experimental Physics Report

    Energy Technology Data Exchange (ETDEWEB)

    Burke, J. T. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Hughes, R. O. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Escher, J. E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Scielzo, N. D. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Casperson, R. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Ressler, J. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Saastamoinen, A. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Ota, S. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Park, H. I. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Ross, T. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); McCleskey, M. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); McCleskey, E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Austin, R. E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Rapisarda, G. G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2017-09-21

    This technical report documents the surrogate reaction method and experimental results used to determine the desired neutron induced cross sections of 87Y(n,g) and the known 90Zr(n,g) cross section. This experiment was performed at the STARLiTeR apparatus located at Texas A&M Cyclotron Institute using the K150 Cyclotron which produced a 28.56 MeV proton beam. The proton beam impinged on Y and Zr targets to produce the nuclear reactions 89Y(p,d)88Y and 92Zr(p,d)91Zr. Both particle singles data and particle-gamma ray coincident data were measured during the experiment. This data was used to determine the γ-ray probability as a function of energy for these reactions. The results for the γ-ray probabilities as a function of energy for both these nuclei are documented here. For completeness, extensive tabulated and graphical results are provided in the appendices.

  4. CERPI and CEREL, two computer codes for the automatic identification and determination of gamma emitters in thermal-neutron-activated samples

    International Nuclear Information System (INIS)

    Giannini, M.; Oliva, P.R.; Ramorino, M.C.

    1979-01-01

    A computer code that automatically analyzes gamma-ray spectra obtained with Ge(Li) detectors is described. The program contains such features as automatic peak location and fitting, determination of peak energies and intensities, nuclide identification, and calculation of masses and errors. Finally, the results obtained with this computer code for a lunar sample are reported and briefly discussed

  5. Determination of Radium 226 in mexican phosphate fertilizers and gypsum by gamma spectrometry

    International Nuclear Information System (INIS)

    Godinez A, M.C.

    1995-01-01

    The 226 Ra isotope was determined in 17, 20 and 46% m/m phosphate fertilizers and gypsum. The samples of the fertilizers were dissolved in 10% v/v nitric acid solutions. The barium sulphate method was used for the precipitation of 226 Ra. On the other hand, alkaline fusion method was used to separate the 226 Ra from gypsum. The results indicated that 226 Ra was present in the phosphate fertilizers and gypsum. The 226 Ra concentrations present in these materials were between 10 -4 - 10 -5 μg g -1 . (Author)

  6. Study of natural diamond detector spectrometric properties under neutron irradiation

    CERN Document Server

    Alekseyev, A B; Kaschuck, Y; Krasilnikov, A; Portnov, D; Tugarinov, S

    2002-01-01

    Natural diamond detector (NDD) performance was studied up to a neutron fluence of 10 sup 1 sup 5 neutron/cm sup 2. The variations of the NDD spectrometric response to incident alpha-particles from sup 2 sup 4 sup 1 Am source after exposure to fast neutron fluences up to 3x10 sup 1 sup 6 n/cm sup 2 were examined. No significant variations up to the level of 10 sup 1 sup 4 n/cm sup 2 were observed. Degradation of charge collection efficiency at higher fluences is reported. No remarkable increase of the NDD leakage current and count rate change had been observed up to a neutron fluence of 3x10 sup 1 sup 6 n/cm sup 2. The charge collection efficiency variations of neutron irradiated diamond spectrometer were studied ex situ under gamma-rays, beta-radiation and visible light excitation. Charge collection efficiency restoration up to 75% level and the NDD performance stabilization by extrinsic low-intensity visible light (550 nm

  7. Determination of plutonium isotopic abundances by gamma-ray spectrometry. Interim report on the status of methods and techniques developed by the Lawrence Livermore Laboratory

    International Nuclear Information System (INIS)

    Gunnink, R.

    1980-03-01

    This report presents an overview of methods and techniques developed by the Lawrence Livermore Laboratory for determining plutonium isotopic abundances from gamma-ray spectra that have been measured with germanium detectors. The methodology of fitting the spectral features includes discussions of algorithms for gamma-ray and x-ray peak shape fitting and generation of response spectra profiles characteristic of specific isotopes. Applications of the techniques developed at government, commercial, and Japanese reprocessing plants are described. Current development of the methodology for the nondestructive analysis of samples containing nondescript solid materials is also presented

  8. A 170Tm gamma scattering technique for the determination of absolute bone density.

    Science.gov (United States)

    Olkkonen, H; Karjalainen, P

    1975-07-01

    A new technique for the determination of absolute bone density is described. The procedure is based on the measurement of both transmitted and scattered photons emitted from a 650 mCi radioisotope source of 170Tm in a narrow beam geometry. The method takes into consideration the change in the effective Z/A as a function of bone density which is due to the changing of the elementary composition of bone when bone material is resorbed. The experimental results show that the density of homogeneous materials can be measured with a reproducibility of 2 per cent. The bone density values for the 24 bone specimens measured by the new method show a good correlation (r=0 with 94) with results obtained by application of Archimedes' principle.

  9. Standardization of radionuclides multi-gamma emitters 166mHo and 72Ga and determination of its gamma intensities by decay

    International Nuclear Information System (INIS)

    Moreira, Denise Simoes

    2005-01-01

    In the present work, the multi-gamma emitters 166m Ho and 72 Ga have been measured by 4πβ-γ coincidence technique. The calibration system is composed of a 4π gas-flow proportional counter coupled to a pair of NaI(Tl) crystals. Both radionuclides were measured by using two gamma discrimination windows, namely (629.9 + 834.2) keV and (2201.6 + 2507.7) keV for 72 Ga and 184.4 keV and (711.7 + 830.5) keV for 166m Ho. The methodology recently developed by LMN (Laboratorio de Metrologia Nuclear) for simulating all detection processes in a 4π(β,X)-γ coincidence system by means of the Monte Carlo technique was applied to the measurements of both radionuclides, and the predict behavior extrapolation curve was compared with the experimental data. The results obtained were in good agreement within the experimental uncertainty. The emission probabilities per decay of the most intense y-ray in the decay of 166m Ho and 72 Ga were measured by means HPGe spectrometer system, which was previously calibrated with standard sources of 57 Co, 60 Co, 54 Mn, 133 Ba, 24 Na, 152E u and 241 Am previously standardized in the 4πβ-γ system. All the uncertainties evolved were treated rigorously, by means of covariance analysis. (author)

  10. Improvement of gamma-ray Sn transport calculations including coherent and incoherent scatterings and secondary sources of bremsstrahlung and fluorescence: Determination of gamma-ray buildup factors

    International Nuclear Information System (INIS)

    Kitsos, S.; Diop, C.M.; Assad, A.; Nimal, J.C.; Ridoux, P.

    1996-01-01

    Improvements of gamma-ray transport calculations in S n codes aim at taking into account the bound-electron effect of Compton scattering (incoherent), coherent scattering (Rayleigh), and secondary sources of bremsstrahlung and fluorescence. A computation scheme was developed to take into account these phenomena by modifying the angular and energy transfer matrices, and no modification in the transport code has been made. The incoherent and coherent scatterings as well as the fluorescence sources can be strictly treated by the transfer matrix change. For bremsstrahlung sources, this is possible if one can neglect the charged particles path as they pass through the matter (electrons and positrons) and is applicable for the energy range of interest for us (below 10 MeV). These improvements have been reported on the kernel attenuation codes by the calculation of new buildup factors. The gamma-ray buildup factors have been carried out for 25 natural elements up to 30 mean free paths in the energy range between 15 keV and 10 MeV

  11. Inactivation of Enterobacter sakazakii in infant milk formula by gamma irradiation: determination of D10-value.

    Science.gov (United States)

    Osaili, T M; Shaker, R R; Abu Al-Hasan, A S; Ayyash, M M; Martin, E M

    2007-04-01

    Enterobacter sakazakii is an emerging foodborne pathogen that has caused several cases of meningitis and necrotizing enterocolitis in infants and has been associated with infant formulas. Five strains of E. sakazakii were inoculated individually into brain heart infusion broth and rehydrated or dehydrated infant milk formula and exposed to ionizing radiation. E. sakazakii strains in brain heart infusion broth and rehydrated infant milk formula (RIMF) were exposed to irradiation dose of up to 1 kGy while strains in dehydrated infant milk formula (DIMF) were exposed to irradiation dose of up to 9 kGy. The D(10)-values were determined by using a linear regression model. Average calculated D(10)-values ranged from 0.21 to 0.29 kGy, 0.24 to 0.37 kGy, and 1.06 to 1.71 kGy in brain heart infusion broth, RIMF, and DIMF, respectively. The results obtained from this study will be useful for powdered infant milk formula industries to reduce the risk associated with E. sakazakii.

  12. Gamma camera

    International Nuclear Information System (INIS)

    Reiss, K.H.; Kotschak, O.; Conrad, B.

    1976-01-01

    A gamma camera with a simplified setup as compared with the state of engineering is described permitting, apart from good localization, also energy discrimination. Behind the usual vacuum image amplifier a multiwire proportional chamber filled with trifluorine bromium methane is connected in series. Localizing of the signals is achieved by a delay line, energy determination by means of a pulse height discriminator. With the aid of drawings and circuit diagrams, the setup and mode of operation are explained. (ORU) [de

  13. Determination of the Interaction Position of Gamma Photons in Monolithic Scintillators Using Neural Network Fitting

    Science.gov (United States)

    Conde, P.; Iborra, A.; González, A. J.; Hernández, L.; Bellido, P.; Moliner, L.; Rigla, J. P.; Rodríguez-Álvarez, M. J.; Sánchez, F.; Seimetz, M.; Soriano, A.; Vidal, L. F.; Benlloch, J. M.

    2016-02-01

    In Positron Emission Tomography (PET) detectors based on monolithic scintillators, the photon interaction position needs to be estimated from the light distribution (LD) on the photodetector pixels. Due to the finite size of the scintillator volume, the symmetry of the LD is truncated everywhere except for the crystal center. This effect produces a poor estimation of the interaction positions towards the edges, an especially critical situation when linear algorithms, such as Center of Gravity (CoG), are used. When all the crystal faces are painted black, except the one in contact with the photodetector, the LD can be assumed to behave as the inverse square law, providing a simple theoretical model. Using this LD model, the interaction coordinates can be determined by means of fitting each event to a theoretical distribution. In that sense, the use of neural networks (NNs) has been shown to be an effective alternative to more traditional fitting techniques as nonlinear least squares (LS). The multilayer perceptron is one type of NN which can model non-linear functions well and can be trained to accurately generalize when presented with new data. In this work we have shown the capability of NNs to approximate the LD and provide the interaction coordinates of γ-photons with two different photodetector setups. One experimental setup was based on analog Silicon Photomultipliers (SiPMs) and a charge division diode network, whereas the second setup was based on digital SiPMs (dSiPMs). In both experiments NNs minimized border effects. Average spatial resolutions of 1.9 ±0.2 mm and 1.7 ±0.2 mm for the entire crystal surface were obtained for the analog and dSiPMs approaches, respectively.

  14. Determination of the gamma-ray flux of the stopped WWR-SM reactor by color center production in LiF

    International Nuclear Information System (INIS)

    Mussaeva, M.A.; Kalannov, M.U.; Ibragimova, E.M.; Karabaev, Kh.Kh.

    2004-01-01

    Full text: Gamma-radiation with a wide energy spectrum, accompanying neutron flux in the nuclear reactor, is known to result in radiation heating of materials. It is usually detected either by calorimetry or by an ionizing chamber maintained in the active zone while the reactor works and high-energy neutrons also contribute into ionization. The aim of this research was to separate the gamma-component from the neutron flux upon stopping the WWR-SM reactor and to determine the gamma-intensity both with the ionization chamber and the well-known dosimeter LiF crystal, and also by comparing with the effect of monochromatic 60 Co gamma-radiation of the known flux and dose. For LiF with small Z the photoelectric effect is weak, and Compton scattering prevails. Both the optical absorption and photo-luminescence techniques together with micro-hardness and X-ray diffraction analysis were used for measuring the structure defect generation rate in the irradiated crystals, which is proportional to the gamma-intensity. Fluorine vacancy trapping electron is the well-known stable F-center responsible for the isolated absorption band at 250 nm and induced by radiolysis mechanism. The sequential irradiations and measurements were done within 150 hours after the moment of the reactor quenching. The dose dependence of the absorption band was found to be linear up to the dose of 10 6 R. The F-center concentration as a measure of an accumulated dose was calculated by the Smakula formula. At higher doses another band at 440 nm appears like that for 60 Co irradiation, which is responsible for unstable F 2 and F 3 centers formed due to coagulation of F-centers. X-diffraction analysis revealed twin structure in (111) plane. Yet the micro-hardness of the gamma-irradiated samples did not change noticeably. For higher doses the photo-luminescence band at 650 nm was also used as a dosimetric item. The luminescence kinetics has a fast nanosecond scale component and a weak tail in a microsecond

  15. Determination of conversion factors between body doses and relevant radiation quantities for external X-ray and gamma irradiation

    International Nuclear Information System (INIS)

    Kramer, R.

    1979-02-01

    With particular consideration of ICRP-26 conversion factors between body doses and relevant radiation quantities for external X- and gamma radiation were assessed. Determination of these conversion factors included all areas of professional, medical, and environmental exposures. There was used a mathematical exposure model being essentially defined by application of a Monte Carlo photon transport calculation in a mathematical human phantom. Body doses were estimated for a reference man in relation to the relevant raditon quantities for different angles of incidence as a function of photon energy. The effective whole body dose defining the risk assessment of stochastic radiation effects was evaluated for the first time. There was also calculated the equivalent dose index which, with respect to radiation protection, is of special importance among the quantities characterizing radiation. The calculations indicated that for different irradiation directions in the energy range between 0.025 and 10 MeV the equivalent dose index gives a conservative estimation for the effective whole body dose. For X-ray diagnostic examinations in the body area the tissue surface dose may be regarded as an upper limit for body doses in the useful beam. The standard energy dose and the equivalent dose index are a conservative measure for important body doses in case of terrestrial radiation and fresh fall-out radiation from the ground. (orig./HP) [de

  16. Gaseous radionuclide activity in the building 6010 exhaust determined by gamma-ray assay of cryogenic liquified samples

    International Nuclear Information System (INIS)

    Dickens, J.K.

    1991-01-01

    Samples of gaseous components in the exhaust stack of Building 6010 at the Oak Ridge National Laboratory were obtained for two conditions, (a) the Oak Ridge Electron Accelerator in a normal operating mode, and (b) the accelerator shut down. The decay of one radionuclide, 222 Rn, was observed equally in both measurements. The decay of three radionuclides, namely 11 C, 13 N and 41 Ar, was observed during accelerator operation but not during shutdown. Gamma-ray assay measurements were obtained using a calibrated, high-resolution, Ge detector system. Background data were obtained to ascertain quantitatively the sample-independent contributions to the measurements. Data reduction utilized a combination of computer and manual methods. A complete analysis was carried out to determine the actual measured isotope radioactivity density (in pCi/ell) for the particular conditions existing at the time the samples were collected. Corrections were applied to these results to account for non-constant sample collection rates and for sample transfer losses. A complete report of all facets of the experiment is given. 20 refs., 9 figs., 5 tabs

  17. Determination of gamma radiation lethal dose (LD{sub 50}) and resveratrol cytotoxicity level in tumor cells line

    Energy Technology Data Exchange (ETDEWEB)

    Magalhaes, Vanessa D.; Rogero, Sizue O.; Rogero, Jose R. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Cruz, Aurea S. [Instituto Adolfo Lutz (IAL-SP) Secao de Culturas Celulares, SP (Brazil)

    2011-07-01

    Cancer is a disease with high incidence and it is considered a worldwide public health problem. Resveratrol is a polyphenol occurring naturally in a wide variety of plants according to response of ultraviolet radiation (UV) exposition or according to mechanical stress resulting of pathogens or chemical and physical agents. This polyphenol possesses a pharmacological activity of carcinogenesis inhibition in multiple levels. It also protects cells by scavenging the free radicals which are considered toxic products. These free radicals are formed of natural process of cell aging and also by incidence of ionizing radiation in the organism. Thus, resveratrol is considered as a cell radioprotector. On the other hand, in some elevated concentrations resveratrol may be considered as a radiosensitizing. The aim of this work was the determination of radiation lethal dose (LD{sub 50}) and also verifies the cytotoxicity level of resveratrol in tumor cells line: muco epidermoid pulmonary carcinoma cells (NCI-H292) and rhabdomyosarcoma cells (RD). The cytotoxicity test was performed by neutral red uptake assay. The results of resveratrol IC{sub 50%} in NCI-H292 cells was 192{mu}M and in RD cells was 128{mu}M; and RD cells gamma radiation LD{sub 50} was 435Gy. (author)

  18. Determination of a cross-sectional void fraction in a tube bundle using a single beam gamma densitometer

    International Nuclear Information System (INIS)

    Guichard, J.; Mezoul, B.; Peturaud, P.; Thomas, B.

    1991-06-01

    In order to qualify 3-dimensional two-phase flow computer codes modelling average flows in tube bundles, cross-section average void fractions must be measured over sub-channels. On the VATICAN mockup, such void fractions(integrated on the mockup thickness) are determined using a single (narrow) beam gamma densitometer. But to avoid a refined exploration of each measurement mesh, for each test, empirical calibration curves have been developed in a regular mesh of the mockup, in axial flow conditions. These calibration curves, which evaluate the sought cross-sectional value as a function of a chordal void fraction (right in the inter-rod gap) depend only on heat flux density and pressure. The data are consistent with the ARMAND-MASSENA and LELLOUCHE-ZOLOTAR slip correlations, and they are fitted by 3rd degree polynomials, for each heat flux density investigated, with a good accuracy. Unfortunately, preliminary testing and analysis indicate that the use of these calibration curves in subcooled boiling and transverse mixing zones might result in significant uncertainties and errors

  19. Determination of Th and U by neutron activation for gamma spectrometry calibration in situ; Determinacion de Th y U por activacion neutronica para calibracion de espectrometria gamma in situ

    Energy Technology Data Exchange (ETDEWEB)

    Nava M, F.; Rios M, C.; Mireles G, F.; Saucedo A, S.; Davila R, I.; Pinedo, J. L. [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98060 Zacatecas (Mexico); Landsberger, S., E-mail: iqnava@hotmail.com [University of Texas at Austin, Nuclear Engineering Teaching Laboratory, Pickle Research Campus, R9000 Austin, Texas 78712 (United States)

    2012-10-15

    Using the analysis by neutron activation to determine the profile of the thorium and uranium concentration calibration factors were obtained for their use in the gamma spectrometry in situ. Three sites were selected (San Ramon, Villa de Cos y la Zacatecana) and the analysis by activation was development in the Laboratory of Nuclear Engineering Teaching of the Texas University in Austin with the nuclear reactor Ut-TRIGA. Starting from the gamma spectra in situ, the areas of normalized photo-pick of the radioisotopes were: {sup 208}Tl and {sup 228}Ac for the thorium series and {sup 214}Pb and {sup 214}Bi for the uranium series. The averages of the factors found in units of (cpm/Bq/Kg) are of 105.63{+-}8.32 and 75.87{+-}4.61 for the thorium and uranium, respectively. (Author)

  20. Precision measurement of $\\sigma(e^+e^-\\rightarrow\\pi^+\\pi^-\\gamma)/\\sigma(e^+e^-\\rightarrow \\mu^+\\mu^-\\gamma)$ and determination of the $\\pi^+\\pi^-$ contribution to the muon anomaly with the KLOE detector

    CERN Document Server

    Babusci, D.; Balwierz-Pytko, I.; Bencivenni, G.; Bini, C.; Bloise, C.; Bossi, F.; Branchini, P.; Budano, A.; Caldeira Balkestahl, L.; Capon, G.; Ceradini, F.; Ciambrone, P.; Curciarello, F.; Czerwinski, E.; Dane, E.; De Leo, V.; De Lucia, E.; De Robertis, G.; De Santis, A.; De Simone, P.; Di Domenico, A.; Di Donato, C.; Domenici, D.; Erriquez, O.; Fanizzi, G.; Felici, G.; Fiore, S.; Franzini, P.; Gauzzi, P.; Giardina, G.; Giovannella, S.; Gonnella, F.; Graziani, E.; Happacher, F.; Heijkenskjold, L.; Hoistad, B.; Iafolla, L.; Iarocci, E.; Jacewicz, M.; Johansson, T.; Kluge, W.; Kupsc, A.; Lee-Franzini, J.; Loddo, F.; Lukin, P.; Mandaglio, G.; Martemianov, M.; Martini, M.; Mascolo, M.; Messi, R.; Miscetti, S.; Morello, G.; Moricciani, D.; Moskal, P.; Muller, S.; Nguyen, F.; Passeri, A.; Patera, V.; Prado Longhi, I.; Ranieri, A.; Redmer, C.F.; Santangelo, P.; Sarra, I.; Schioppa, M.; Sciascia, B.; Silarski, M.; Taccini, C.; Tortora, L.; Venanzoni, G.; Versaci, R.; Wislicki, W.; Wolke, M.; Zdebik, J.

    2013-01-01

    We have measured the ratio $\\sigma(e^+e^-\\rightarrow\\pi^+\\pi^-\\gamma)/\\sigma(e^+e^-\\rightarrow \\mu^+\\mu^-\\gamma)$, with the KLOE detector at DA$\\Phi$NE for a total integrated luminosity of $\\sim$ 240 pb$^{-1}$. From this ratio we obtain the cross section $\\sigma(e^+e^-\\rightarrow\\pi^+\\pi^-)$. From the cross section we determine the pion form factor $|F_\\pi|^2$ and the two-pion contribution to the muon anomaly $a_\\mu$ for $0.592

  1. ALMERA Proficiency Test: Determination of Gamma Emitting Radionuclides in Simulated Air Filters

    International Nuclear Information System (INIS)

    2010-01-01

    The activity concentration of radionuclides in air is a critical factor in assessing the air quality and the potential impact of possible pollutants. Air is in fact one of the main pathways for human exposure to radioactivity. Radioactivity may be present in the atmosphere due to natural processes; intentional (low level) anthropogenic release; or as a consequence of nuclear or radiological incident. The resulting environmental impact should be considered carefully to ensure safety and compliance with environmental regulations. A reliable determination of radionuclides in air is necessary for regular monitoring of air quality to comply with radiation protection and environmental regulations. This proficiency test (PT) is one of the series of the ALMERA network proficiency tests organised on regular basis by the Terrestrial Environment Laboratory in Seibersdorf, designed to assess the technical capacity of ALMERA Members in analysing radionuclides to identify any analytical problems and to support ALMERA laboratories to maintain their preparedness to provide rapid and reliable analytical results. The range of simulated air filters used in this PT for analysis has been mainly at environmental level. The PT set consisted of four filters. The participating laboratories were requested to analyze Mn-54, Co-57, Fe-59, Co-60, Zn-65, Cd-109, Ba-133, Cs-134, Cs-137, Eu-152 and Am-241 in filters 01, 02 and 03. The participants were informed that only some of the listed radionuclides were present in the filters and the levels of the radionuclides were such that they could be measured within a 6-hour measurement period using a conventional HPGe gammaspectrometer of 35% relative efficiency. Filter 04, was containing only Co-60 and Ba-133 with known activities to the participants, had to be used as a control for the efficiency calibration. The tasks of IAEA were to prepare and distribute the simulated air filters to the participating laboratories, to collect and interpret

  2. Determination iodine in biological materials using instrumental neutron activation and anti-coincidence gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Zhang, W.H.; Chatt, A.

    1997-01-01

    Iodine is an element of interest in nutritional research. Its lower limit of safe and adequate daily dietary intake for adults varies between 150 and 200 micrograms per day. In the present study, an epithermal instrumental neutron activation analysis (EINAA) method in conjunction with anti-coincidence counting has been developed for the determination of ppb levels of iodine in individual food items. Typically 200-300 mg of a sample are irradiated for 10 or 20 minutes at the Dalhousie University SLOWPOKE-2 reactor in an epithermal flux of 1x10 11 n cm -2 s -1 , followed by 1 min decay and then counting for 30 min. The 443-keV gamma-ray of 128 I is used for measuring iodine content by anti-coincidence counting. The anti-coincidence spectrometer consists of a 25% HPGe detector surrounded by a 10''x10'' NaI(TI) annulus and a 3''x3'' NaI(TI) plug. This system has a peak-to-Compton ratio of about 650 to 1 for the 661.6-keV photopeak of 137 Cs. The Compton background resulting from the scattering of many gamma-rays of energies higher than 443 keV can be reduced by a factor of about 4 using anti-coincidence counting compared to conventional counting. The detection limit for iodine can be improved by a factor of 2 to 5 depending on the sample matrix, dead time, position of the annulus and counting geometry among several other factors.The lowest detection limit of 5 ppb can be achieved for low-salt foods. This limit is comparable to that obtained by a preconcentration NAA (PNAA) method. However, a detection limit of 20 ppb is more realistic for samples containing high amounts of Na, Cl and Al. The results obtained for many reference materials are in good agreement with the certified values and those reported by the PNAA method. Details of the methods and results will be reported

  3. Determination iodine in biological materials using instrumental neutron activation and anti-coincidence gamma-ray spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, W.H.; Chatt, A. [Dalhousie University, Halifax, Nova Scotia (Canada). Radiochemistry Research Laboratory

    1997-10-01

    Iodine is an element of interest in nutritional research. Its lower limit of safe and adequate daily dietary intake for adults varies between 150 and 200 micrograms per day. In the present study, an epithermal instrumental neutron activation analysis (EINAA) method in conjunction with anti-coincidence counting has been developed for the determination of ppb levels of iodine in individual food items. Typically 200-300 mg of a sample are irradiated for 10 or 20 minutes at the Dalhousie University SLOWPOKE-2 reactor in an epithermal flux of 1x10{sup 11} n cm{sup -2} s{sup -1}, followed by 1 min decay and then counting for 30 min. The 443-keV gamma-ray of {sup 128}I is used for measuring iodine content by anti-coincidence counting. The anti-coincidence spectrometer consists of a 25% HPGe detector surrounded by a 10``x10`` NaI(TI) annulus and a 3``x3`` NaI(TI) plug. This system has a peak-to-Compton ratio of about 650 to 1 for the 661.6-keV photopeak of {sup 137}Cs. The Compton background resulting from the scattering of many gamma-rays of energies higher than 443 keV can be reduced by a factor of about 4 using anti-coincidence counting compared to conventional counting. The detection limit for iodine can be improved by a factor of 2 to 5 depending on the sample matrix, dead time, position of the annulus and counting geometry among several other factors.The lowest detection limit of 5 ppb can be achieved for low-salt foods. This limit is comparable to that obtained by a preconcentration NAA (PNAA) method. However, a detection limit of 20 ppb is more realistic for samples containing high amounts of Na, Cl and Al. The results obtained for many reference materials are in good agreement with the certified values and those reported by the PNAA method. Details of the methods and results will be reported 6 refs., 2 tabs.

  4. Natural gamma radioactivity and of {sup 137} Cs in soil of the Chimaltitan municipality, Jalisco, Mexico; Radiactividad gamma natural y del {sup 137} Cs en suelo del Municipio de Chimaltitan, Jalisco, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Garay, A.; Mireles, F.; Quirino, L.L.; Davila, J.I.; Rios, C.; Lugo, J.F.; Soriano, J.M.; Angoli, A. [UAEN-Universidad Autonoma de Zacatecas, Cipres 10, Frac. La Penuela, 98000 Zacatecas (Mexico)]. e-mail: albinogaray@hotmail.com.mx

    2003-07-01

    With the purpose of determining the activity due to the natural presence of the {sup 226} Ra, {sup 232} Th, {sup 40} K and {sup 137} Cs in soil samples, of the municipality of Chimaltitan Jalisco. A set of these samples was measured in a gamma ray spectrometric system based on a High-purity Germanium detector. It is well-known that approximately 87% of the dose of the received radiation by the population is due to sources of natural radiation and 13% of the anthropogenic radiation. The gamma radiation comes mainly from the {sup 40} K and of those radionuclides of the series of radioactive decay of {sup 238} U and {sup 232} Th that its find dispersed thoroughly in the terrestrial crust. In this work its were analyzed twenty-two soil samples. It is enlarged the activity characterization for the radioisotopes of {sup 226} Ra {sup 232} Th, {sup 40} K and {sup 137} Cs. (Author)

  5. [Value of the determination of gamma glutamyl transpeptidase in the detection of hepatic metastases of bronch-pulmonary cancers].

    Science.gov (United States)

    Leguay, G; Lafargue, P; Marbot, P; Rassouly, C; Droniou, J; Kermarec, J; Pernod, J

    1975-01-01

    The authors have dosed gamma glutamyl transpeptidase in 42 patients with primary bronchopulmonary cancer, of whom 14 had liver metastases. In these 14 patients the level of gamma glutamyl transpeptidase was always high, except in 1 case; while in the remaining lot, a moderate and mostly belated increase was noticed in only 32 percent of cases. The dosing of gamma glutamyl transpeptidase present some interest in the detection of liver metastases in primary bronchopulmonary cancers, specially when coupled with the dosing of alcaline phosphatase. Interpretation of results should take into account the existence of an associated liver-gall bladder involvement and of a recent surgical operation; both factors being capable of raising the level of gamma glutamyl transpeptidase.

  6. Determination of the optimum-size californium-252 neutron source for borehole capture gamma-ray analysis

    Science.gov (United States)

    Senftle, F.E.; Macy, R.J.; Mikesell, J.L.

    1979-01-01

    The fast- and thermal-neutron fluence rates from a 3.7 ??g 252Cf neutron source in a simulated borehole have been measured as a function of the source-to-detector distance using air, water, coal, iron ore-concrete mix, and dry sand as borehole media. Gamma-ray intensity measurements were made for specific spectral lines at low and high energies for the same range of source-to-detector distances in the iron ore-concrete mix and in coal. Integral gamma-ray counts across the entire spectrum were also made at each source-to-detector distance. From these data, the specific neutron-damage rate, and the critical count-rate criteria, we show that in an iron ore-concrete mix (low hydrogen concentration), 252Cf neutron sources of 2-40 ??g are suitable. The source size required for optimum gamma-ray sensitivity depends on the energy of the gamma ray being measured. In a hydrogeneous medium such as coal, similar measurements were made. The results show that sources from 2 to 20 ??g are suitable to obtain the highest gamma-ray sensitivity, again depending on the energy of the gamma ray being measured. In a hydrogeneous medium, significant improvement in sensitivity can be achieved by using faster electronics; in iron ore, it cannot. ?? 1979 North-Holland Publishing Co.

  7. Computer application in a nondestructive testing device for determining 235U enrichment

    International Nuclear Information System (INIS)

    Liu Yun

    1997-01-01

    The hardware multichannel is replaced by a computer multichannel analyzer in the second generation of nondestructive testing device for determining 235 U enrichment of fuel element in nuclear power plant. The spectrometric analyzer system consists of the spectrometric analysis board and the multichannel emulator software (PHA). The multichannel scaling system is composed of eight-channel multichannel scaling board and the multichannel scaling software (MCS). The digital discrimination, self-tracing and self-adjusting of threshold energy, and two-peak and two-window techniques are used to increase the measuring accuracy and testing speed. The automatic loading and unloading and classification of fuel rods are realized by using computer, therefore, the level of automation is upgraded. The method of on-line inspection of rods enrichment with passive gamma-ray can play its role fully due to the application of computer in the second generation of nondestructive testing device. (4 figs., 1 tab.)

  8. Mass spectrometric examinations of Hungarian triassic dolomites

    International Nuclear Information System (INIS)

    Vitalis, Gy.; Kada I-ne

    1982-01-01

    A limited number of mass spectrometric investigations (viz.:57) of representative rock types were applied both in the research work of geology and the mining for the industry of building materials of Hungary. Tabulated results covering all rock types and all stratigraphic levels of the Hungarian Triassic are given. Sr, Mn, Ti and Cr trace elements had the highest occurrence and Zn, Y or Pb, Ba, V or Cu, depending on the genetical type of the rock studied, has relatively higher concentrations as well. The results of the examinations of Hungarian Triassic dolomites were discussed according to genetical types, all represented by a small level of trace elements. (Sz.J.)

  9. Evaluation of mass spectrometric techniques for characterization of engineered proteins

    DEFF Research Database (Denmark)

    Roepstorff, P; Schram, K H; Andersen, Jens S.

    1995-01-01

    Mass spectrometric characterization of engineered proteins has been examined using bovine recombinant Acyl-CoA-Binding Protein (rACBP), [15N]-labeled rACBP, and a number of sequence variants of ACBP produced by site-directed mutagenesis. The mass spectrometric techniques include ESIMS and MALDIMS...

  10. Mass Spectrometric Studies of Oxides

    Science.gov (United States)

    Jacobson, Nathan S.

    2012-01-01

    Current studies at NASA Glenn on oxide thermodynamics are discussed. Previous studies on the vaporization of B2O3 in reducing atmospheres led to inconsistent studies when B was used as a reductant. It is shown that liquid B2O3 does not wet B and a clear phase separation was noted in the Knudsen cell. This problem was solved by using FeB and Fe2B to supply a different and constant activity of B. The thermodynamic data thus derived are compared to quantum chemical composite calculations. A major problem in high temperature mass spectrometry is the determination of accurate ionization cross sections, particularly for molecules. The method of Deutsch and Mark shows promise and some sample calculations are discussed. Finally current studies on the thermodynamics of rare earth silicates are discussed. Here the problems are obtaining a measurable signal from SiO2 vaporization and non-equilibrium vaporization. The use of a Ta reducing agent provides a stronger signal, which is related to silica activity. The Whitman-Motzfeld relation adapted to KEMS measurements is applied to obtain equilibrium pressures.

  11. Determination of the $e^+ e^- \\to \\gamma \\gamma(\\gamma)$ cross-section at centre-of-mass energies ranging from 189 GeV to 202 GeV

    CERN Document Server

    Abreu, P.; Adye, T.; Adzic, P.; Albrecht, Z.; Alderweireld, T.; Alekseev, G.D.; Alemany, R.; Allmendinger, T.; Allport, P.P.; Almehed, S.; Amaldi, U.; Amapane, N.; Amato, S.; Anassontzis, E.G.; Andersson, P.; Andreazza, A.; Andringa, S.; Antilogus, P.; Apel, W.D.; Arnoud, Y.; Asman, B.; Augustin, J.E.; Augustinus, A.; Baillon, P.; Ballestrero, A.; Bambade, P.; Barao, F.; Barbiellini, G.; Barbier, R.; Bardin, D.Yu.; Barker, G.J.; Baroncelli, A.; Battaglia, M.; Baubillier, M.; Becks, K.H.; Begalli, M.; Behrmann, A.; Beilliere, P.; Belokopytov, Yu.; Belous, K.; Benekos, N.C.; Benvenuti, A.C.; Berat, C.; Berggren, M.; Berntzon, L.; Bertrand, D.; Besancon, M.; Bilenky, Mikhail S.; Bizouard, M.A.; Bloch, D.; Blom, H.M.; Bonesini, M.; Boonekamp, M.; Booth, P.S.L.; Borisov, G.; Bosio, C.; Botner, O.; Boudinov, E.; Bouquet, B.; Bourdarios, C.; Bowcock, T.J.V.; Boyko, I.; Bozovic, I.; Bozzo, M.; Bracko, M.; Branchini, P.; Brenner, R.A.; Bruckman, P.; Brunet, J.M.; Bugge, L.; Buran, T.; Buschbeck, B.; Buschmann, P.; Cabrera, S.; Caccia, M.; Calvi, M.; Camporesi, T.; Canale, V.; Carena, F.; Carroll, L.; Castillo Gimenez, M.V.; Cattai, A.; Cavallo, F.R.; Chapkin, M.; Charpentier, P.; Checchia, P.; Chelkov, G.A.; Chierici, R.; Shlyapnikov, P.; Chochula, P.; Chorowicz, V.; Chudoba, J.; Cieslik, K.; Collins, P.; Contri, R.; Cortina, E.; Cosme, G.; Cossutti, F.; Costa, M.; Crawley, H.B.; Crennell, D.; Crosetti, G.; Cuevas Maestro, J.; Czellar, S.; D'Hondt, J.; Dalmau, J.; Davenport, M.; Da Silva, W.; Della Ricca, G.; Delpierre, P.; Demaria, N.; De Angelis, A.; De Boer, W.; De Clercq, C.; De Lotto, B.; De Min, A.; De Paula, L.; Dijkstra, H.; Di Ciaccio, L.; Dolbeau, J.; Doroba, K.; Dracos, M.; Drees, J.; Dris, M.; Eigen, G.; Ekelof, T.; Ellert, M.; Elsing, M.; Engel, J.P.; Espirito Santo, M.C.; Fanourakis, G.; Fassouliotis, D.; Feindt, M.; Fernandez, J.; Ferrer, A.; Ferrer-Ribas, E.; Ferro, F.; Firestone, A.; Flagmeyer, U.; Foeth, H.; Fokitis, E.; Fontanelli, F.; Franek, B.; Frodesen, A.G.; Fruhwirth, R.; Fulda-Quenzer, F.; Fuster, J.; Galloni, A.; Gamba, D.; Gamblin, S.; Gandelman, M.; Garcia, C.; Gaspar, C.; Gaspar, M.; Gasparini, U.; Gavillet, P.; Gazis, Evangelos; Gele, D.; Geralis, T.; Ghodbane, N.; Gil Botella, Ines; Glege, F.; Gokieli, R.; Golob, B.; Gomez-Ceballos, G.; Goncalves, P.; Gonzalez Caballero, I.; Gopal, G.; Gorn, L.; Guz, Yu.; Gracco, V.; Grahl, J.; Graziani, E.; Gris, P.; Grosdidier, G.; Grzelak, K.; Guy, J.; Haag, C.; Hahn, F.; Hahn, S.; Haider, S.; Hajduk, Z.; Hallgren, A.; Hamacher, K.; Hansen, J.; Harris, F.J.; Hauler, F.; Hedberg, V.; Heising, S.; Hernandez, J.J.; Herquet, P.; Herr, H.; Higon, E.; Holmgren, S.O.; Holt, P.J.; Hoorelbeke, S.; Houlden, M.; Hrubec, J.; Huber, M.; Hughes, G.J.; Hultqvist, K.; Jackson, John Neil; Jacobsson, R.; Jalocha, P.; Janik, R.; Jarlskog, C.; Jarlskog, G.; Jarry, P.; Jean-Marie, B.; Jeans, D.; Johansson, Erik Karl; Jonsson, P.; Joram, C.; Juillot, P.; Jungermann, L.; Kapusta, Frederic; Karafasoulis, K.; Katsanevas, S.; Katsoufis, E.C.; Keranen, R.; Kernel, G.; Kersevan, B.P.; Khokhlov, Yu.A.; Khomenko, B.A.; Khovansky, N.N.; Kiiskinen, A.; King, B.; Kinvig, A.; Kjaer, N.J.; Klapp, O.; Kluit, P.; Kokkinias, P.; Kostyukhin, V.; Kourkoumelis, C.; Kuznetsov, O.; Krammer, M.; Kriznic, E.; Krumshtein, Z.; Kubinec, P.; Kucewicz, W.; Kurowska, J.; Kurvinen, K.; Lamsa, J.W.; Lane, D.W.; Lapin, V.; Laugier, J.P.; Lauhakangas, R.; Leder, G.; Ledroit, Fabienne; Leinonen, L.; Leisos, A.; Leitner, R.; Lemonne, J.; Lenzen, G.; Lepeltier, V.; Lethuillier, M.; Libby, J.; Liebig, W.; Liko, D.; Lipniacka, A.; Lippi, I.; Lorstad, B.; Loken, J.G.; Lopes, J.H.; Lopez, J.M.; Lopez-Fernandez, R.; Loukas, D.; Lutz, P.; Lyons, L.; MacNaughton, J.; Mahon, J.R.; Maio, A.; Malek, A.; Maltezos, S.; Malychev, V.; Mandl, F.; Marco, J.; Marco, R.; Marechal, B.; Margoni, M.; Marin, J.C.; Mariotti, C.; Markou, A.; Martinez-Rivero, C.; Marti i Garcia, S.; Masik, J.; Mastroyiannopoulos, N.; Matorras, F.; Matteuzzi, C.; Matthiae, G.; Mazzucato, F.; Mazzucato, M.; McCubbin, M.; McKay, R.; McNulty, R.; McPherson, G.; Merle, E.; Meroni, C.; Meyer, W.T.; Myagkov, A.; Migliore, E.; Mirabito, L.; Mitaroff, W.A.; Mjornmark, U.; Moa, T.; Moch, M.; Moller, Rasmus; Monig, Klaus; Monge, M.R.; Moraes, D.; Morettini, P.; Morton, G.; Muller, U.; Munich, K.; Mulders, M.; Mulet-Marquis, C.; Mundim, L.M.; Muresan, R.; Murray, W.J.; Muryn, B.; Myatt, G.; Myklebust, T.; Naraghi, F.; Nassiakou, M.; Navarria, F.L.; Nawrocki, K.; Negri, P.; Neufeld, N.; Nicolaidou, R.; Nielsen, B.S.; Niezurawski, P.; Nikolenko, M.; Nomokonov, V.; Nygren, A.; Oblakowska Mucha, A.; Obraztsov, V.; Olshevsky, A.G.; Onofre, A.; Orava, R.; Orazi, G.; Osterberg, K.; Ouraou, A.; Oyanguren, A.; Paganoni, M.; Paiano, S.; Pain, R.; Paiva, R.; Palacios, J.; Papadopoulou, T.D.; Pape, L.; Parkes, C.; Parodi, F.; Parzefall, U.; Passeri, A.; Passon, O.; Pavel, T.; Pegoraro, M.; Peralta, L.; Pernicka, M.; Perrotta, A.; Petridou, C.; Petrolini, A.; Phillips, H.T.; Pierre, F.; Pimenta, M.; Piotto, E.; Podobnik, T.; Poireau, V.; Pol, M.E.; Polok, G.; Poropat, P.; Pozdnyakov, V.; Privitera, P.; Pukhaeva, N.; Pullia, A.; Radojicic, D.; Ragazzi, S.; Rahmani, H.; Rames, J.; Ratoff, P.N.; Read, Alexander L.; Rebecchi, P.; Redaelli, Nicola Giuseppe; Regler, M.; Rehn, J.; Reid, D.; Reinertsen, P.; Reinhardt, R.; Renton, P.B.; Resvanis, L.K.; Richard, F.; Ridky, J.; Rinaudo, G.; Ripp-Baudot, Isabelle; Romero, A.; Ronchese, P.; Rosenberg, E.I.; Rosinsky, P.; Roudeau, P.; Rovelli, T.; Ruhlmann-Kleider, V.; Ruiz, A.; Saarikko, H.; Sacquin, Y.; Sadovsky, A.; Sajot, G.; Salt, J.; Sampsonidis, D.; Sannino, M.; Savoy-Navarro, A.; Schwemling, P.; Schwering, B.; Schwickerath, U.; Scuri, Fabrizio; Seager, P.; Sedykh, Yu.; Segar, A.M.; Seibert, N.; Sekulin, R.; Sette, G.; Shellard, R.C.; Siebel, M.; Simard, L.; Simonetto, F.; Sisakian, A.N.; Smadja, G.; Smirnova, O.; Smith, G.R.; Solovianov, O.; Sopczak, A.; Sosnowski, R.; Spassoff, T.; Spiriti, E.; Squarcia, S.; Stanescu, C.; Stanitzki, M.; Stevenson, K.; Stocchi, A.; Strauss, J.; Strub, R.; Stugu, B.; Szczekowski, M.; Szeptycka, M.; Tabarelli, T.; Taffard, A.; Tegenfeldt, F.; Terranova, F.; Timmermans, Jan; Tinti, N.; Tkachev, L.G.; Tobin, M.; Todorova, S.; Tome, B.; Tonazzo, A.; Tortora, L.; Tortosa, P.; Transtromer, G.; Treille, D.; Tristram, G.; Trochimczuk, M.; Troncon, C.; Turluer, M.L.; Tyapkin, I.A.; Tyapkin, P.; Tzamarias, S.; Ullaland, O.; Uvarov, V.; Valenti, G.; Vallazza, E.; Van Dam, Piet; Van Den Boeck, W.; Van Eldik, J.; Van Lysebetten, A.; Van Remortel, N.; Van Vulpen, I.; Vegni, G.; Ventura, L.; Venus, W.; Verbeure, F.; Verdier, P.; Verlato, M.; Vertogradov, L.S.; Verzi, V.; Vilanova, D.; Vitale, L.; Vlasov, E.; Vodopianov, A.S.; Voulgaris, G.; Vrba, V.; Wahlen, H.; Washbrook, A.J.; Weiser, C.; Wicke, D.; Wickens, J.H.; Wilkinson, G.R.; Winter, M.; Wolf, G.; Yi, J.; Yushchenko, O.; Zalewska, A.; Zalewski, P.; Zavrtanik, D.; Zevgolatakos, E.; Zimine, N.I.; Zinchenko, A.; Zoller, P.; Zumerle, G.; Zupan, M.

    2000-01-01

    A test of the QED process \\eeintogg(\\fot) is reported. The data analysed were collected with the DELPHI detector in 1998 and 1999 at the highest ener\\-gies achieved at LEP, reaching 202 GeV in the centre-of-mass. The total integrated luminosity amounts to 375.7 pb$^{-1}$. The differential and total cross-sections for the process $e^+e^- \\to \\gamma \\gamma$ were measured, and found to be in agreement with the QED prediction. 95\\% Confidence Level (C.L.) lower limits on the QED cut-off parameters of $\\rm \\Lambda_+ >$ 330 GeV and $\\rm \\Lambda_{-}>$ 320 GeV were derived. A 95\\% C.L. lower bound on the mass of an excited electron of 311 $\\rm GeV/c^2$ (for $\\lambda_{\\gamma}$ =1) was obtained. s-channel virtual graviton exchange was searched for, resulting in 95\\% C.L. lower limits on the string mass scale, $\\rm M_S$: $\\rm M_S > 713 \\, GeV/c^2$ ( $\\lambda=1$) and $\\rm M_S > 691 \\,GeV/c^2$ ($\\lambda = -1$).

  12. Social and neural determinants of aggressive behavior: pharmacotherapeutic targets at serotonin, dopamine and gamma-aminobutyric acid systems.

    Science.gov (United States)

    Miczek, Klaus A; Fish, Eric W; De Bold, Joseph F; De Almeida, Rosa M M

    2002-10-01

    Aggressive outbursts that result in harm and injury present a major problem for the public health and criminal justice systems, but there are no adequate treatment options. Obstacles at the level of social policy, institutional regulation, and scientific strategy in developing animal models continue to impede the development of specific anti-aggressive agents for emergency and long-term treatments. To be more relevant to the clinical situation, preclinical aggression research has begun to focus on the neurobiological determinants of escalated aggressive behavior that exceeds species-typical patterns. It is the goal of this review to examine novel pharmacological and molecular tools that target the neural mechanisms for different kinds of aggressive behavior more selectively than previously possible and to outline potential pharmacotherapeutic options. (1) The preclinical focus on the behavioral characteristics and determinants of intense aggression promises to be most relevant to the clinical distinction between the proposed impulsive-reactive-hostile-affective subtypes of human aggression and the controlled-proactive-instrumental-predatory subtypes of aggression. The neural circuits for many types of human and animal aggression critically involve serotonin, dopamine and gamma-aminobutyric acid (GABA) and specific receptor subtypes. (2) The dynamic changes in frontal cortical serotonin that are triggered by engaging in aggressive behavior imply that serotonergic drug effects are largely determined by the functional state of the receptors at the time of drug treatment. Of the numerous 5-HT receptors currently identified, the 5-HT(1B) receptors offer a promising target for reducing impulsive aggressive behavior, particularly if the action can be limited to sites in the central nervous system. (3) Aggressive confrontations are salient stressors, both for the aggressor as well as the victim of aggression, that are accompanied by activation of the mesocorticolimbic but

  13. ESR identification of {gamma}-irradiated redoxon and determination of ESR parameters of radicals produced in irradiated ascorbic acid

    Energy Technology Data Exchange (ETDEWEB)

    Polat, Mustafa [Physics Engineering Department, Hacettepe University, Beytepe, 06800 Ankara (Turkey)]. E-mail: polat@hacettepe.edu.tr; Korkmaz, Mustafa [Physics Engineering Department, Hacettepe University, Beytepe, 06800 Ankara (Turkey)

    2005-04-11

    In the present work, electron spin resonance (ESR) identification of irradiated redoxon and its potential use as a normal and/or accidental dosimetric material were investigated in details. The ground redoxon samples exhibited a single weak resonance line of peak-to-peak width {delta}H{sub pp} = 0.9 mT appearing at g = 2.0057. {gamma}-Radiation produced many resonance lines beside four different intense lines (denoted as I{sub 1}, I{sub 2}, I{sub 3} and I{sub 4}) of different spectral features in the studied dose range of 2.5-25 kGy. Experimental dose-response curves associated with I{sub 1}, I{sub 2}, I{sub 3} and I{sub 4} resonance lines were found to follow an exponential function. From stability and kinetic studies at room and above room temperatures it was concluded that radicals contributing to I{sub 3} and I{sub 4} resonance lines were more stable than the radical species contributing to I{sub 1} and I{sub 2} resonance lines. Simulation calculations based on the room temperature ESR intensity data of an ascorbic acid (active ingredient of redoxon) sample irradiated at 10 kGy was performed to determine the structure and spectral parameters of the radiation-induced radical species involved in the formation of experimental ESR spectrum of ascorbic acid. The contributions of these species to the ESR spectrum of irradiated redoxon were discussed.

  14. Study of the gamma spectrum of 16N with a BGO detector, for the purpose of calibration and of determining the fluorine grade of mineral samples

    International Nuclear Information System (INIS)

    Castro-Garcia, M.P.; Alonso-Sanchez, T.; Rey-Ronco, M.A.

    2013-01-01

    The study of 16 N's gamma spectrum has two main uses: calibrating gamma detectors in a high energy range, and determining the fluorine grade of mineral samples of fluorite. This article examines and compares the gamma ray spectrum of 16 N as recorded by a Bi 4 GeO 12 detector, as well as the resolution of this detector at high energy levels, and the signal-background relationship of an experimental laboratory cyclic activation unit. 16 N is the product of the reaction 9-F-19(n,α)7-N-16, which takes place during the neutron activation of mineral samples of fluorspar, and its production depends, among other factors, upon the grade of fluorite. The technique used in this study is cyclic-type neutron activation for recording delayed gamma rays, carried out with an americium-beryllium neutron source with an activity of 1 Ci. Lastly, a correlation is established between the area below the peak amount of 16 N emitted by the sample, and the sample's fluorite grade. (author)

  15. Suitable gamma ray dose determination in order to induce genetic variation in kaboli chickpea (Cicer Arietinum L)

    International Nuclear Information System (INIS)

    Naserian Khiabani, B.; Ahari Mostafavi, H.; Fathollahi, H.; Vedadi, S.; Mosavi Shalmani, M. A.

    2008-01-01

    In spite of chickpea's use in Iran and its ability of being replaced to adjust the shortage of protein in dietary habits, yield production is very low. One of the main reasons for chickpea's low yield production is its sensitiveness to some diseases, pest and environmental stresses. Genetic variation in chickpea is very low, because of its self pollination. In breeding programs, genetic variation plays an essential role so that the induction of genetic variation in plant population is very important for the plant breeders. The induced mutation through different kinds of mutagens is one of the important ways of genetic variation. In this research, first the sensitiveness of four cultivars (ILC.486, Philip86, Bivinich, Jam) were assessed to different gamma ray doses (100, 200, 300, 400 Gy). The results showed that with an increase in gamma ray dose, the growth rate of chickpea's genotypes decreases. In this respect, the decrease of growth rate has a linear relationship with the gamma ray dose and it is independent from the genotypes. The root length is more sensitive to gamma ray doses than its shoot, and it was observed that at the low doses the root growth decreases, comparing to the shoot growth. On the other hand, in high doses of gamma ray growth abrasion (Ageotropism, Albinism and etc.) were observed. Some traits variation (such as leaf shape, leaf size, leaf color, Albinism, etc.) were seen in M 2 generation, and finally to continue the project, three doses of gamma ray (150,200,250) were selected for the next year

  16. Dose Determination using alanine detectors in a Mixed Neutron and Gamma Field for Boron Neutron Capture Therapy of Liver Malignancies

    DEFF Research Database (Denmark)

    Schmitz, T.; Blaickner, M.; Ziegner, M.

    2011-01-01

    be suitable for measurements in mixed neutron and gamma fields. Materials and Methods Two experiments have been carried out in the thermal column of the TRIGA Mark II reactor at the University of Mainz. Alanine dosimeters have been irradiated in a phantom and in liver tissue. Results For the interpretation......, in combination with flux measurements and Monte Carlo calculations with FLUKA, suggest that it is possible to establish a system for monitoring the dose in a mixed neutron and gamma field for BNCT and other applications in radiotherapy....

  17. $\\beta$3$p$-spectroscopy and proton-$\\gamma$ width determination in the decay of $^{31}$Ar

    CERN Multimedia

    We propose to perform a detailed study of the $\\beta$-decay of the dripline nucleus $^{31}$Ar. This will allow a detailed study of the $\\beta$-delayed 3$p$-decay as well as provide important information on the resonances of $^{30}$S and $^{29}$P, in particular the ratio between the $p$- and $\\gamma$- partial widths relevant for astrophysics.

  18. Determination of natural radioactive elements in building materials by gamma spectroscopy, trace dosimetry and neutron activation analysis

    International Nuclear Information System (INIS)

    Perez, G.; Desdin, L.F.; Hernandez, A.T.; Gonzalez, D.; Labrada, A.; Tenreiro, J.J.; Capote, G.; Perelyguin, V.P.; Herrera, H.; Tellez, E.

    1993-01-01

    Five types of Cuban concretes and their main components (minerals aggregates and cement) were investigated in order to analyze the content of uranium, thorium, radium, potassium and radon 220,222, using gamma spectroscopy, trace dosimetry and neutron activation analysis. The comparative evaluation of different concretes, aggregates and two types of cements according to natural radioactivity is shown

  19. System for gamma-gamma formation density logging while drilling

    International Nuclear Information System (INIS)

    Paske, W.C.

    1991-01-01

    The patent relates to a system for logging subterranean formations for the determination of formation density by using gamma radiation. Gamma ray source and detection means are disposed within a housing adapted for positioning within a borehole for the emission and detection of gamma rays propagating through earth formations and borehole drilling fluid. The gamma ray detection means comprises first and second gamma radiation sensors geometrically disposed within the housing, the same longitudinal distance from the gamma ray source and diametrically opposed in a common plane. A formation matrix density output signal is produced in proportion to the output signal from each of the gamma ray sensors and in conjunction with certain constants established by the geometrical configuration of the sensors relative to the gamma ray source and the borehole diameter. Formation density is determined without regard to the radial position of the logging probe within the borehole in a measuring while drilling mode. 6 figs

  20. Production of 16N and obtaining of its gamma spectrum in order to calibrate detectors or determination of fluorine in geological specimens

    International Nuclear Information System (INIS)

    Rey-Ronco, M.A.; Alonso-Sanchez, T.; Castro-Garcia, M.P.

    2010-01-01

    In this paper, we show a procedure for producing 16 N and a method to obtain its gamma spectrum with a NaI(Tl) detector. We also demonstrate the interest of this radioactive element for the purpose of NaI(Tl) detector calibration and for the determination of fluorine in geological specimens using an Alpha Beryllium neutron source. This work consists of a theoretical study which analyzes the characteristics of 16 N and nuclear reactions that originate from an Americium Beryllium source of 1Ci activity. We justify our choice of reaction 19 F(n,α) 16 N and the use of fluorspar as a source of fluorine. The mathematical procedure followed to obtain the gamma rays spectrum produced by 16 N in a NaI(Tl) detector is shown.

  1. Production of {sup 16}N and obtaining of its gamma spectrum in order to calibrate detectors or determination of fluorine in geological specimens

    Energy Technology Data Exchange (ETDEWEB)

    Rey-Ronco, M.A., E-mail: rey@uniovi.e [Departamento de Energia, Universidad de Oviedo, 33004 Oviedo (Spain); Alonso-Sanchez, T., E-mail: tjalonso@uniovi.e [Departamento de Explotacion y Prospeccion de Minas, Universidad de Oviedo, 33004 Oviedo (Spain); Castro-Garcia, M.P., E-mail: UO21947@uniovi.e [Departamento de Explotacion y Prospeccion de Minas, Universidad de Oviedo, 33004 Oviedo (Spain)

    2010-09-15

    In this paper, we show a procedure for producing {sup 16}N and a method to obtain its gamma spectrum with a NaI(Tl) detector. We also demonstrate the interest of this radioactive element for the purpose of NaI(Tl) detector calibration and for the determination of fluorine in geological specimens using an Alpha Beryllium neutron source. This work consists of a theoretical study which analyzes the characteristics of {sup 16}N and nuclear reactions that originate from an Americium Beryllium source of 1Ci activity. We justify our choice of reaction {sup 19}F(n,{alpha}){sup 16}N and the use of fluorspar as a source of fluorine. The mathematical procedure followed to obtain the gamma rays spectrum produced by {sup 16}N in a NaI(Tl) detector is shown.

  2. A Determination of the Intergalactic Redshift Dependent UV-Optical-NIR Photon Density Using Deep Galaxy Survey Data and the Gamma-ray Opacity of the Universe

    Science.gov (United States)

    Stecker, Floyd W.; Malkan, Matthew A.; Scully, Sean T.

    2012-01-01

    We calculate the intensity and photon spectrum of the intergalactic background light (IBL) as a function of redshift using an approach based on observational data obtained in many different wavelength bands from local to deep galaxy surveys. This allows us to obtain an empirical determination of the IBL and to quantify its observationally based uncertainties. Using our results on the IBL, we then place 68% confidence upper and lower limits on the opacity of the universe to gamma-rays, free of the theoretical assumptions that were needed for past calculations. We compare our results with measurements of the extragalactic background light and upper limits obtained from observations made by the Fermi Gamma-ray Space Telescope.

  3. Gamma spectrometry for chronology of recent sediments

    Energy Technology Data Exchange (ETDEWEB)

    Pittauerova, Daniela

    2013-12-17

    This thesis deals with several aspects of gamma spectrometric analysis of natural and artificial isotopes in sediments and their use as tracers for qualification and quantification of accumulation and mixing processes in different aquatic environments. Sediment cores from three distinct areas including terrigenous sediments deposited on the continental slope off NW Africa, deep sea sediments off Sumba Island and five stations from the Gulf of Eilat in the Red Sea area were measured and interpreted within this dissertation. The main concern in gamma spectrometry of voluminous environmental samples is a reliable efficiency calibration. This is specially relevant for the analysis of low energy gamma emitters (<100 keV). {sup 210}Pb, an important isotopic tracer to cover the period of the last century, is one of them. Within this work mathematical efficiency calibration was applied using a commercial software package. A series of validation tests was performed and evaluated for point and voluminous samples. When using {sup 210}Pb as a tracer it is necessary to determine its excess portion, which is not supported by ingrowth from the parent nuclide {sup 226}Ra. Its analysis is mostly performed via short lived daughter isotopes that follow after the intermediate gaseous member {sup 222}Rn. Preventing the escape of radon from the sample is a critical step before analysis due to a negative effect of supported {sup 210}Pb underestimation on the chronology, which was also documented in this thesis. Time series registering ingrowth of {sup 214}Pb and {sup 214}Bi towards radioactive equilibrium with {sup 226}Ra in different containers were evaluated for analyses of {sup 226}Ra. Direct analyses of {sup 226}Ra was compared to its detection via daughter products. A method for aligning parallel radionuclide depth profiles was described and applied successfully in two case studies from the continental slope off NW Africa and off Sumba Island, Indonesia. This is primarily important

  4. Gamma spectrometry for chronology of recent sediments

    International Nuclear Information System (INIS)

    Pittauerova, Daniela

    2013-01-01

    This thesis deals with several aspects of gamma spectrometric analysis of natural and artificial isotopes in sediments and their use as tracers for qualification and quantification of accumulation and mixing processes in different aquatic environments. Sediment cores from three distinct areas including terrigenous sediments deposited on the continental slope off NW Africa, deep sea sediments off Sumba Island and five stations from the Gulf of Eilat in the Red Sea area were measured and interpreted within this dissertation. The main concern in gamma spectrometry of voluminous environmental samples is a reliable efficiency calibration. This is specially relevant for the analysis of low energy gamma emitters (<100 keV). 210 Pb, an important isotopic tracer to cover the period of the last century, is one of them. Within this work mathematical efficiency calibration was applied using a commercial software package. A series of validation tests was performed and evaluated for point and voluminous samples. When using 210 Pb as a tracer it is necessary to determine its excess portion, which is not supported by ingrowth from the parent nuclide 226 Ra. Its analysis is mostly performed via short lived daughter isotopes that follow after the intermediate gaseous member 222 Rn. Preventing the escape of radon from the sample is a critical step before analysis due to a negative effect of supported 210 Pb underestimation on the chronology, which was also documented in this thesis. Time series registering ingrowth of 214 Pb and 214 Bi towards radioactive equilibrium with 226 Ra in different containers were evaluated for analyses of 226 Ra. Direct analyses of 226 Ra was compared to its detection via daughter products. A method for aligning parallel radionuclide depth profiles was described and applied successfully in two case studies from the continental slope off NW Africa and off Sumba Island, Indonesia. This is primarily important when combined profiles obtained from short

  5. Liquid chromatography-tandem mass spectrometric assay for the nucleoside reverse transcriptase inhibitor emtricitabine in human plasma

    NARCIS (Netherlands)

    Sparidans, Rolf W.; Prins, Jan M.; Schellens, Jan H. M.; Beijnen, Jos H.

    2007-01-01

    A liquid chromatography-tandem mass spectrometric assay for the determination of the antiretroviral nucleoside emtricitabine in human plasma was developed and validated using a simple sample pre-treatment procedure. After addition of 5'-deoxy-5-fluorocytidine as the internal standard and protein

  6. A new technique for the determination of impurities in uranium-and thorium compounds, by the analysis of capture gamma rays

    International Nuclear Information System (INIS)

    Pecequilo, B.R.S.

    1978-01-01

    A new technique is presented for the determination of impurities in uranium-and thorium compounds, based on the analysis of capture gamma rays emitted by the impurities and by the matrix element, without previous matrix isolation. The experimental system utilized is described and calibration curves are given. Several measurements are made for uranium oxide and thorium oxide samples to which known impurities were added in a controlled way: Through the analysis of spectra, the possibility is shown of utilizing the new technique for the determination of impurities found in uranium-and thorium compounds used as nuclear fuel materials. (Author) [pt

  7. Standard test methods for chemical, mass spectrometric, and spectrochemical analysis of nuclear-grade boron carbide

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2004-01-01

    1.1 These test methods cover procedures for the chemical, mass spectrometric, and spectrochemical analysis of nuclear-grade boron carbide powder and pellets to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Sections Total Carbon by Combustion and Gravimetry 7-17 Total Boron by Titrimetry 18-28 Isotopic Composition by Mass Spectrometry 29-38 Chloride and Fluoride Separation by Pyrohydrolysis 39-45 Chloride by Constant-Current Coulometry 46-54 Fluoride by Ion-Selective Electrode 55-63 Water by Constant-Voltage Coulometry 64-72 Impurities by Spectrochemical Analysis 73-81 Soluble Boron by Titrimetry 82-95 Soluble Carbon by a Manometric Measurement 96-105 Metallic Impurities by a Direct Reader Spectrometric Method 106-114

  8. Determination of trace metal ions via on-line separation and preconcentration by means of chelating Sepharose beads in a sequential injection lab-on-valve (SI-LOV) system coupled to electrothermal atomic absorption spectrometric detection

    DEFF Research Database (Denmark)

    Long, Xiangbao; Hansen, Elo Harald; Miró, Manuel

    2005-01-01

    The analytical performance of an on-line sequential injection lab-on-valve (SI-LOV) system using chelating Sepharose beads as sorbent material for the determination of ultra trace levels of Cd(II), Pb(II) and Ni(II) by electrothermal atomic absorption spectrometry (ETAAS) is described and discussed...

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

    International Nuclear Information System (INIS)

    Samsahl, K.

    1964-12-01

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

  10. Determination of the changes of antifungal properties of Satureja hortensis, Thymus vulgaris and Thymbra spicata exposed to gamma irradiation

    Science.gov (United States)

    Gumus, Tuncay

    2010-01-01

    In this research, changes in the antifungal activity of the extract of Satureja hortensis, Thymus vulgaris and Thymbra spicata exposed to gamma irradiation against two aflatoxigenic moulds Aspergillus parasiticus NRRL 2999 and 465 were investigated. The samples of dry plant leaf powder were irradiated with doses of 1.2, 3.0, 5.1 kGy. While the antifungal activity of S. hortensis with 0 and 1.2 kGy dose irradiation against A. parasiticus NRRL 2999 was found to be similar, it decreased with 3.0 and 5.1 kGy irradiation doses ( Pvulgaris, an increase of irradiation dose resulted in a decrease of antifungal activity against aflatoxigenic moulds. This research shows that antifungal properties of some spices can be changed by gamma irradiation.

  11. Dosimetric studies, spectrometric, radiographic, metallographic of a new argentinean seed of 125 I used in brachytherapy

    International Nuclear Information System (INIS)

    Pirchio, R.; Saravi, M.; Banchik, D.; Munoz, C.

    2006-01-01

    A new source of 125 I model Braquibac TM has been developed in Argentina for applications in interstitial brachytherapy. The AAPM Task Group 43 (TG-43) recommends that dosimetric characteristics of new sources of brachytherapy of Iodine-125 have been theoretically and experimentally determined before its clinical use. The objectives outlined in this work were the study of the design of the new seed, the calculation of dosimetric parameters and the photons spectra analysis. Its were carried out radiographic and metallographic studies to determine the physical characteristics of the source. For the realization of the dosimetric calculations it was used the Monte Carlo code MCNP5. Values of the radial dose function, g(r), of the constant of dose rate, Λ, of the function of anisotropy of two dimensions, F(r, θ), of the factor and constant of anisotropy its were obtained simulating the source in water according to the recommended methodology in TG-43. The constant of dose rate is similar to 0,880 ± 0,080 c Gy h -1 U -1 . The kerma in air rate of reference, S K , was calculated as 1,036 c Gy cm 2 h -1 mCi -1 simulating the seed in dry air. Its were carried out spectrometric studies using a semiconductor planar detector of HPGe (high purity germanium). Photons spectra showed characteristic x-rays of 125 I with energies of 27,20 keV, 27,47 keV, 31 keV and 31,70 keV gamma photons of 35,5 keV, and x-ray fluorescent coming from the silver nucleus of 22,10 keV, 24,94 keV and 25,45 keV. The angular dependence of the intensity of photons around the seed and in air it was analyzed with the planar detector. This was carried out to study the anisotropy in the photons flow due to variation in the thickness of the titanium wall and of the welding, movements of the silver tube inside the source and deposition of the radioactive material on the silver tube. (Author)

  12. Gas chromatographic-mass spectrometric separation, identification and determination of C6-C12 cyclic imides in thermally treated epoxy and alkyd resins to locate hot spots inside large electricity generators.

    Science.gov (United States)

    Husain, S; Alvi, S N; Rao, R N

    1999-11-05

    A simple and rapid GC-MS method for separation, identification and quantitative determination of long-chain cyclic imides in the 300 degrees C thermally treated epoxy and alkyd resins has been developed. The method provides a positive means of identifying C6-C12 cyclic imide derivatives by GC-MS and enables the specific area of overheating to be identified, thereby averting catastrophic failures of power generators in service.

  13. Development of particle induced gamma-ray emission methods for nondestructive determination of isotopic composition of boron and its total concentration in natural and enriched samples.

    Science.gov (United States)

    Chhillar, Sumit; Acharya, Raghunath; Sodaye, Suparna; Pujari, Pradeep K

    2014-11-18

    We report simple particle induced gamma-ray emission (PIGE) methods using a 4 MeV proton beam for simultaneous and nondestructive determination of the isotopic composition of boron ((10)B/(11)B atom ratio) and total boron concentrations in various solid samples with natural isotopic composition and enriched with (10)B. It involves measurement of prompt gamma-rays at 429, 718, and 2125 keV from (10)B(p,αγ)(7)Be, (10)B(p, p'γ)(10)B, and (11)B(p, p'γ)(11)B reactions, respectively. The isotopic composition of boron in natural and enriched samples was determined by comparing peak area ratios corresponding to (10)B and (11)B of samples to natural boric acid standard. An in situ current normalized PIGE method, using F or Al, was standardized for total B concentration determination. The methods were validated by analyzing stoichiometric boron compounds and applied to samples such as boron carbide, boric acid, carborane, and borosilicate glass. Isotopic compositions of boron in the range of 0.247-2.0 corresponding to (10)B in the range of 19.8-67.0 atom % and total B concentrations in the range of 5-78 wt % were determined. It has been demonstrated that PIGE offers a simple and alternate method for total boron as well as isotopic composition determination in boron based solid samples, including neutron absorbers that are important in nuclear technology.

  14. On-line complexation of zinc with 5-Br-PADAP and preconcentration using a knotted reactor for inductively coupled plasma atomic emission spectrometric determination in river water samples

    Energy Technology Data Exchange (ETDEWEB)

    Salonia, J.A.; Wuilloud, R.G.; Gasquez, J.A.; Olsina, R.A.; Martinez, L.D. [Area de Quimica Analitica, Facultad de Quimica, Bioquimica y Farmacia, Universidad Nacional de San Luis, Chacabuco y Pedernera, 5700 San Luis (Argentina)

    2000-08-01

    An on-line zinc preconcentration and determination system implemented with inductively coupled plasma atomic emission spectrometry (ICP-AES) associated with flow injection (FI) was studied. The zinc was retained as zinc-2-(5-bromo-2-pyridylazo)-5-diethylaminophenol (Zn-(5-Br-PADAP)) complex at pH 9.2. The zinc complex was removed from the knotted reactor (KR) with 30% v/v nitric acid. An enrichment factor of 42 was obtained for the KR system with respect to ICP-AES using pneumatic nebulization. The detection limit for the preconcentration of 10 mL of aqueous solution was 0.09 {mu}g/L. The precision for 10 replicate determinations at the 5 {mu}g/L Zn level was 2.3% relative standard deviation (RSD), calculated with the peak heights obtained. The calibration graph using the preconcentration system for zinc was linear with a correlation coefficient of 0.9997 at levels near the detection limits up to at least 100 {mu}g/L. The method was succesfully applied to the determination of zinc in river water samples. (orig.)

  15. Experimental determination of gamma radiation effect from cobalt 60 on the viscosity of SSBR-B polymer

    International Nuclear Information System (INIS)

    Santos, L.G. dos; Silva Filho, E.

    1989-01-01

    Samples of the polymer known as SSBR-B (Solution Styrenne Butadiene Rubber-Blockade) were irradiated with gamma rays from a 60 Co source. Viscosity analysis performed by using the method of Ostwald Showed that the viscosity remains about constant for doses in the range of zero to 11560 Gray (Gy). For doses greater than 11560 Gy the viscosity increases. This result characterizes an irradiation induced hardening of the polymer. (author) [pt

  16. Simultaneous determination of exponential background and Gaussian peak functions in gamma ray scintillation spectrometers by maximum likelihood technique

    International Nuclear Information System (INIS)

    Eisler, P.; Youl, S.; Lwin, T.; Nelson, G.

    1983-01-01

    Simultaneous fitting of peaks and background functions from gamma-ray spectrometry using multichannel pulse height analysis is considered. The specific case of Gaussian peak and exponential background is treated in detail with respect to simultaneous estimation of both functions by using a technique which incorporates maximum likelihood method as well as a graphical method. Theoretical expressions for the standard errors of the estimates are also obtained. The technique is demonstrated for two experimental data sets. (orig.)

  17. Quantitative Determination of Radionuclides by Double-Headed Gamma Camera:A Phantom Study with Potential Clinical Applications

    International Nuclear Information System (INIS)

    Golan, H.; Melloul, M.; Presler, O.; Alfassi, Z.B.

    2002-01-01

    The position and activity of an organ can be found using single photon emission computed Tomography (SPECT).However,SPECT imaging is longer and more complicated due to the large number of counting steps and the reconstruction process.Since many gamma cameras nowadays are double-headed,it is important to see if such systems can allow this measurement without the need for SPECT. In measurement of a radioactive source by a non-collimated radiation detector,the distance between the source and the detector is affecting the count rate due to two factors (1)Increasing the distance,decreases the solid angle in which the detector sees the source,therefore decreases the count rate.(2)The absorption of the gamma rays in the medium between the source and the detector depends on the medium length.The larger the absorption length,less photons are reaching the detectors. In the case of gamma camera with collimators only parallel rays to the collimator holes should reach the detector,and hence it is expected that there will be no effect due to change in the solid angle and the only effect of varying the distance between the detectors would be due to absorption in the medium. This study was taken in order to check if this is true for the 140 keV gamma ray of 99m Tc, the main radionuclide used in nuclear medicine,and if this can be used for finding the location and activity of a radioactive source

  18. Determination of the rod-wise fission gas release fraction in a complete fuel assembly using non-destructive gamma emission tomography

    Science.gov (United States)

    Holcombe, Scott; Andersson, Peter; Svärd, Staffan Jacobsson; Hallstadius, Lars

    2016-11-01

    A gamma tomography instrument has been developed at the Halden Boiling Water Reactor (HBWR) in cooperation between the Institute for Energy Technology, Westinghouse (Sweden) and Uppsala University. The instrument is used to record the gamma radiation field surrounding complete fuel assemblies and consists of a shielded enclosure with fixtures to accurately position the fuel and detector relative to each other. A High Purity Germanium detector is used for acquiring high-resolution spectroscopic data, allowing for analysis of multiple gamma-ray peaks. Using the data extracted from the selected peaks, tomographic reconstruction algorithms are used to reproduce the corresponding spatial gamma-ray source distributions within the fuel assembly. With this method, rod-wise data can be can be deduced without the need to dismantle the fuel. In this work, the tomographic device has been experimentally benchmarked for non-destructive rod-wise determination of the Fission Gas Release (FGR) fraction. Measurements were performed on the fuel-stack and gas-plenum regions of a complete fuel assembly, and quantitative tomographic reconstructions of the measurement data were performed in order to determine the rod-wise ratio of 85Kr in the gas plenum to 137Cs in the fuel stack. The rod-wise ratio of 85Kr/137Cs was, in turn, used to calculate the rod-wise FGR fraction. In connection to the tomographic measurements, the fuel rods were also measured individually using gamma scanning in order to provide an experimental benchmark for the tomographic method. Fuel rods from two donor driver fuel assemblies were placed into a nine-rod HBWR driver fuel assembly configuration. In order to provide a challenging measurement object and thus an appropriate benchmark for the tomographic method, five rods were taken from an assembly with a burnup of 51 MWd/kgUO2, and four rods were from an assembly with a burnup of 26 MWd/kgUO2. At the time of the measurements, the nine rods had cooled for

  19. Energy dispersive X-Ray fluorescence spectrometric study of ...

    African Journals Online (AJOL)

    Energy dispersive X-Ray fluorescence spectrometric study of compositional differences in trace elements in dried Moringa oleifera leaves grown in two different agro-ecological locations in Ebonyi State, Nigeria.

  20. The use of emulsions for the determination of methylmercury and inorganic mercury in fish-eggs oil by cold vapor generation in a flow injection system with atomic absorption spectrometric detection.

    Science.gov (United States)

    Burguera, J L; Quintana, I A; Salager, J L; Burguera, M; Rondón, C; Carrero, P; Anton de Salager, R; Petit de Peña, Y

    1999-04-01

    An on-line time based injection system used in conjunction with cold vapor generation atomic absorption spectrometry and microwave-aided oxidation with potassium persulfate has been developed for the determination of the different mercury species in fish-eggs oil samples. A three-phase surfactant-oil-water emulsion produced an advantageous flow when a peristaltic pump was used to introduce the highly viscous sample into the system. The optimum proportion of the oil-water mixture ratio was 2:3 v/v with a Tween 20 surfactant concentration in the emulsion of 0.008% v/v. Inorganic mercury was determined after reduction with sodium borohydride while total mercury was determined after an oxidation step with persulfate prior to the reduction step to elemental mercury with the same reducing agent. The difference between total and inorganic mercury determined the organomercury content in samples. A linear calibration graph was obtained in the range 0.1-20 micrograms l-1 of Hg2+ by injecting 0.7 ml of samples. The detection limits based on 3 sigma of the blank signals were 0.11 and 0.12 microgram l-1 for total and inorganic mercury, respectively. The relative standard deviation of ten independent measurements were 2.8 and 2.2% for 10 micrograms l-1 and 8.8 and 9.0% for 0.1 microgram l-1 amounts of total and inorganic mercury, respectively. The recoveries of 0.3, 0.6 and 8 micrograms l-1 of inorganic and organic mercury added to fish-eggs oil samples ranged from 93.0 to 94.8% and from 100 to 106%, respectively. Good agreement with those values obtained for total mercury content in real samples by electrothermal atomic absorption spectrometry was also obtained, differences between mean values were catfish-eggs oil samples from the northwestern coast of Venezuela were measured; while the organic mercury lay in the range 2.0 and 3.3 micrograms l-1, inorganic mercury was not detected.

  1. Heteronuclear relayed E.COSY revisited: determination of 3J(H(alpha),C(gamma)) couplings in Asx and aromatic residues in proteins.

    Science.gov (United States)

    Löhr, F; Pérez, C; Köhler, R; Rüterjans, H; Schmidt, J M

    2000-09-01

    Constant-time 3D heteronuclear relayed E.COSY [Schmidt et al. (1996) J. Biomol. NMR, 7, 142-152], as based on generic 2D small-flip-angle HMQC-COSY [Schmidt et al. (1995) J. Biomol. NMR, 6, 95-105], has been modified to allow for quantitative determination of heteronuclear three-bond 3J(H(alpha),C(gamma)) couplings. The method is applicable to amino acid spin topologies with carbons in the gamma position which lack attached protons, i.e. to asparagine, aspartate, and aromatic residues in uniformly 13C-enriched proteins. The pulse sequence critically exploits heteronuclear triple-quantum coherence (HTQC) of CH2 moieties involving geminal H(beta) proton pairs, taking advantage of improved multiple-quantum relaxation properties, at the same time avoiding scalar couplings between those spins involved in multiple-quantum coherence, thus yielding E.COSY-type multiplets with a splitting structure that is simpler than with the original scheme. Numerical least-squares 2D line-shape simulation is used to extract 3J(H(alpha),C(gamma)) coupling constants which are of relevance to side-chain chi1 dihedral-angle conformations in polypeptides. Methods are demonstrated with recombinant 15N,13C-enriched ribonuclease T1 and Desulfovibrio vulgaris flavodoxin with bound oxidized FMN.

  2. Terrestrial gamma radiation dose study to determine the baseline for environmental radiological health practices in Melaka state, Malaysia

    International Nuclear Information System (INIS)

    Ramli, Ahmad Termizi; Sahrone, Sallehudin; Wagiran, Husin

    2005-01-01

    Environmental terrestrial gamma radiation dose rates were measured throughout Melaka, Malaysia, over a period of two years, with the objective of establishing baseline data on the background radiation level. Results obtained are shown in tabular, graphic and cartographic form. The values of terrestrial gamma radiation dose rate vary significantly over different soil types and for different underlying geological characteristics present in the study area. The values ranged from 54 ± 5 to 378 ± 38 nGy h -1 . The highest terrestrial gamma dose rates were measured over soil types of granitic origin and in areas with underlying geological characteristics of an acid intrusive (undifferentiated) type. An isodose map of terrestrial gamma dose rate in Melaka was drawn by using the GIS application 'Arc View'. This was based on data collected using a NaI(Tl) scintillation detector survey meter. The measurements were taken at 542 locations. Three small 'hot spots' were found where the dose rates were more than 350 nGy h -1 . The mean dose rates in the main population areas in the mukims (parishes) of Bukit Katil, Sungai Udang, Batu Berendam, Bukit Baru and Bandar Melaka were 154 ± 15, 161 ± 16, 160 ± 16, 175 ± 18 and 176 ± 18 nGy h -1 , respectively. The population-weighted mean dose rate throughout Melaka state is 172 ± 17 nGy h -1 . This is lower than the geographical mean dose rate of 183 ± 54 nGy h -1 . The lower value arises from the fact that most of the population lives in the central area of the state where the lithology is dominated by sedimentary rocks consisting of shale, mudstone, phyllite, slate, hornfels, sandstone and schist of Devonian origin which have lower associated dose rates. The mean annual effective dose to the population from outdoor terrestrial gamma radiation was estimated to be 0.21 mSv. This value is higher than the world average of 0.07 mSv

  3. Solid Phase Extraction of Trace Al(III), Fe(II), Co(II), Cu(II), Cd(II) and Pb(II) Ions in Beverages on Functionalized Polymer Microspheres Prior to Flame Atomic Absorption Spectrometric Determinations.

    Science.gov (United States)

    Berber, Hale; Alpdogan, Güzin

    2017-01-01

    In this study, poly(glycidyl methacrylate-methyl methacrylate-divinylbenzene) was synthesized in the form of microspheres, and then functionalized by 2-aminobenzothiazole ligand. The sorption properties of these functionalized microspheres were investigated for separation, preconcentration and determination of Al(III), Fe(II), Co(II), Cu(II), Cd(II) and Pb(II) ions using flame atomic absorption spectrometry. The optimum pH values for quantitative sorption were 2 - 4, 5 - 8, 6 - 8, 4 - 6, 2 - 6 and 2 - 3 for Al(III), Fe(II), Co(II), Cu(II), Cd(II) and Pb(II), respectively, and also the highest sorption capacity of the functionalized microspheres was found to be for Cu(II) with the value of 1.87 mmol g -1 . The detection limits (3σ; N = 6) obtained for the studied metals in the optimal conditions were observed in the range of 0.26 - 2.20 μg L -1 . The proposed method was successfully applied to different beverage samples for the determination of Al(III), Fe(II), Co(II), Cu(II), Cd(II) and Pb(II) ions, with the relative standard deviation of <3.7%.

  4. Determination of activity by gamma spectrometry of radionuclides present in drums of residues generated in nuclear centrals; Determinacion de actividad por espectrometria gamma de radionucleidos presentes en tambores de residuos generados en centrales nucleares

    Energy Technology Data Exchange (ETDEWEB)

    Aguiar, J.C.; Fernandez, J. [Autoridad Regulatoria Nuclear, Av. Del Libertador 8250, Ciudad Autonoma de Buenos Aires (Argentina)]. e-mail: jaguiar@cae.arn.gov.ar

    2006-07-01

    The generation of radioactive residuals in nuclear centrals as CNA I (Atucha I Nuclear Central) and CNE (Embalse Nuclear Central) makes that the measurement of those radionuclides has been a previous stage to the waste management. A method used in those nuclear centrals it is the gamma spectrometry with HPGe detectors, previous to the immobilization of the residual in a cemented matrix, with this the contact with the external agents and its possible dispersion to the atmosphere in the short term is avoided. The ARN (Nuclear Regulatory Authority) of Argentina it carries out periodically intercomparisons and evaluations of the measurement and procedures systems used in the nuclear power stations for the correct measurement and determination of activity of radioactive residuals by gamma spectrometry. In this work an independent method of measurement is exposed to the nuclear power stations. To determine the activity of the residuals by gamma spectrometry deposited in drums, it is required of the precise knowledge of the efficiency curve for such geometry and matrix. Due to the RNA doesn't have a pattern of these characteristics, a mathematical model has been used to obtain this efficiency curve. For it, it is necessary to determine previously: 1) the geometric efficiency or solid angle sustained by the source-detector system (drum-detector) applying a mathematical model described in this work. 2) To estimate the auto-attenuation factor that present the photons in the cemented matrix, these calculations are carried out with a simple equation and its are verified with the Micro Shield 6.10 program. The container commonly used by these nuclear power stations its are drums for 220 liters constructed with SAE 1010 steel and with a thickness of 0.127 cm, with an approximate weight 7.73 Kg., internal diameter of 57.1 cm, and height: 87 cm. The results obtained until the moment register a discrepancy from 5 to 10% with relationship to the measurements carried out by the

  5. Comparison of serum copper determination by colorimetric and atomic absorption spectrometric methods in seven different laboratories. The S.F.B.C. (Société Française de Biologie Clinique) Trace Element Group.

    Science.gov (United States)

    Arnaud, J; Chappuis, P; Zawislak, R; Houot, O; Jaudon, M C; Bienvenu, F; Bureau, F

    1993-02-01

    An interlaboratory collaborative trial was conducted on the determination of serum copper using two different methods, based on colorimetry (test combination Copper, Boehringer Mannheim, Mannheim, Germany) and flame atomic absorption spectrometry (FAAS). The general performance of the colorimetric method was below that of FAAS, except for sensitivity and linear range, as assessed by detection limit (0.44 versus 1.32 mumol/L) and upper limit of linearity (150 versus 50 mumol/L). The range of the between-run CVs and the recovery of standard additions were, respectively, 2.3-11.9% and 92-127% for the colorimetric method and 1.1-6.0% and 93-101% for the FAAS method. Interferences were minimal with both methods. The two techniques correlated satisfactorily (the correlation coefficients ranged from 0.945-0.970 among laboratories) but the colorimetric assay exhibited slightly higher results than the FAAS method. Each method was transferable among laboratories.

  6. Diffractive Photon Production in $\\gamma p$ and $\\gamma \\gamma$ Interactions

    CERN Document Server

    Evanson, N G

    1999-01-01

    We study the diffractive production of photons in gamma-p and gamma-gamma collisions. We specifically compute the rates for gamma*-p -> gamma-X and for gamma*-gamma* -> gamma-gamma, where X denotes the proton dissociation. We focus on the rates at large momentum transfers, -t >> Lambda^2, where we are most confident in the use of QCD perturbation theory. However, our calculations do allow us to study the -t -> 0 behaviour of the gamma*-gamma*-> gamma-gamma process in the region where the incoming photons are sufficiently virtual.

  7. Liquid chromatography tandem mass spectrometric determination of triterpenes in human fluids: Evaluation of markers of dietary intake of olive oil and metabolic disposition of oleanolic acid and maslinic acid in humans.

    Science.gov (United States)

    Pozo, Oscar J; Pujadas, Mitona; Gleeson, Sarah Biel; Mesa-García, Maria Dolores; Pastor, Antoni; Kotronoulas, Aristotelis; Fitó, Montserrat; Covas, Maria-Isabel; Navarro, José Ramón Fernández; Espejo, Juan Antonio; Sanchez-Rodriguez, Estefania; Marchal, Rosa; Calleja, Miguel Angel; de la Torre, Rafael

    2017-10-16

    Olive oil is rich in several minor components like maslinic (MA) and oleanolic (OA) acids which have cardioprotective, antitumor, and anti-inflammatory properties. In order to assess the health benefits in humans provided by the olive oil triterpenes (MA and OA), suitable analytical methods able to quantify the low concentrations expected in human fluids are required. In this study, the LC-MS/MS quantification of both OA and MA in plasma and urine has been evaluated. The plasmatic method is based on the direct determination of the analytes. The urinary detection requires more sensitivity which was reached by derivatization with 2-picolylamine. Additionally, the urinary species present after MA and OA ingestion were evaluated by the direct detection of several phase II metabolites previously synthesized. Our results showed that OA is metabolized as both sulfate and glucuronide conjugates whereas MA is mainly excreted as glucuronide. Based on this information, the method for the urinary detection of MA and OA involved an enzymatic hydrolysis. Both plasmatic and urinary methods were validated with suitable precision and accuracy at all tested levels. Required sensitivity was achieved in both matrices. Up to our knowledge, this is the first method able to quantify the low concentration levels of triterpenes present in urine. Samples from two healthy volunteers who received virgin olive oils with different triterpenes content were analyzed. Some preliminary clues on the metabolic disposition of OA and MA after olive oil intake are provided. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Spectrometric estimation of sample amount in aliquot for a direct solid sampling system and its application to the determination of trace impurities in silver nanoparticles by ETV-ICP-OES.

    Science.gov (United States)

    Nakata, Kenichi; Okamoto, Yasuaki; Ishizaka, Syoji; Fujiwara, Terufumi

    2016-04-01

    A method based on a tungsten boat furnace vaporiser, tungsten sample cuvettes, and an inductively coupled plasma (ICP) optical emission spectrometer has been developed for the direct determination of silicon, phosphorus, and sulphur in silver nanoparticles. The important point in the proposed method is that the entire sample in each batch is vaporised, which enables simultaneous measurement of the emission of not only the analyte but also the silver matrix. Furthermore, since the silver nanoparticles are sufficiently pure, the contribution of impurities to the sample amounts will be negligible. Therefore, this estimation is suitable for measuring the sample amount in each aliquot instead of the conventional weighing procedure using a microbalance; therefore, no tedious weighing procedures for estimating the sample amount introduced into the ETV device are needed. An additional advantage is that pretreatment and/or predigestion are unnecessary. The sample throughput is approximately 35 batches per hour. The detection limits of silicon, phosphorus, and sulphur in the silver nanoparticles (dry powder) are 15, 4.2, and 62 µg g(-1), respectively. Analytical results for various silver nanoparticles as both dry particles and in suspended solutions are described, and these values are compared to those obtained by conventional weighing with a microbalance. This methodology is useful for rapid screening and accurate analysis of silver nanoparticles, especially for industrial applications. Copyright © 2015 Elsevier B.V. All rights reserved.

  9. Solid phase extraction of cadmium on 2-mercaptobenzothiazole loaded on sulfur powder in the medium of ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate and cold vapor generation-atomic absorption spectrometric determination

    International Nuclear Information System (INIS)

    Pourreza, N.; Ghanemi, K.

    2010-01-01

    A novel solid phase extractor for preconcentration of cadmium at ng L -1 levels has been developed. Cadmium ions were retained on a column packed with sulfur powder modified with 2-mercaptobenzothiazole (2-MBT) in the medium of 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim] + PF 6 - ) ionic liquid. The presence of ionic liquid during modification of sulfur enhanced the retention of cadmium ions on the column. The retained cadmium ions were eluted with 2 mol L -1 solution of HCl and measured by cold vapor generation-atomic absorption spectrometry (CVG-AAS). By using reaction cell-gas liquid separator (RC-GLS), gaseous cadmium vapors were produced and reached the atomic absorption spectrometer, instantaneously. The influence of different variables on both processes of solid phase extraction and CVG-AAS determination of cadmium ions was investigated. The calibration curve was linear in the range of 10-200 ng L -1 of cadmium in the initial solution with r = 0.9992 (n = 8) under optimum conditions. The limit of detection based on three times the standard deviation of the blank (3S b , n = 10) was 4.6 ng L -1 . The relative standard deviation (R.S.D.) of 25 and 150 ng L -1 of cadmium was 4.1 and 2.2% (n = 8), respectively. The procedure was validated by the analysis of a certified reference material (DORM-3), water and fish samples.

  10. Mass fragmentographic determination of gamma-aminobutyric acid and glutamic acid in discrete amygdaloid nuclei of rat brain.

    Science.gov (United States)

    Nakamura, K; Matsumoto, T; Hirano, M; Kagoshima, H; Kuroki, T; Yao, H; Uchimura, H; Nakahara, T

    1987-06-01

    A mass fragmentographic method for the simultaneous quantification of gamma-aminobutyric acid (GABA) and glutamic acid is described. In a convenient one-step reaction, the two amino acids were derivatized with pentafluoropropionic anhydride and pentafluoropropanol. The derivatization products were stable for several days. The technique has been applied to the assay of GABA and Glu in five amygdaloid nuclei of the rat brain. The GABA level was high in the central and medial nuclei, whereas the Glu level was high in the lateral and basal nuclei. The regional distribution of GABA was different from that of Glu within the amygdaloid nuclei.

  11. Determination of the Integral/SPI instrumental response and his application to the observation of gamma ray lines in the Vela region; Determination de la reponse instrumentale du spectrometre INTEGRAL/SPI et application a l'observation des raies gamma de la region des Voiles

    Energy Technology Data Exchange (ETDEWEB)

    Attie, D

    2005-01-15

    The INTEGRAL/SPI spectrometer was designed to observe the sky in the energy band of 20 keV to 8 MeV. The specificity of instrument SPI rests on the excellent spectral resolution (2.3 keV with 1 MeV) of its detecting plan, composed of 19 cooled germanium crystals; covering an effective area of 508 cm{sup 2}. The use of a coded mask, located at 1.7 m above the detection plan ensures to it a resolving power of 2.5 degrees. The aim of this thesis, begun before the INTEGRAL launch, is made up of two parts. The first part relates to the analysis of the spectrometer calibration data. The objective was to measure and check the performances of the telescope, in particular to validate simulations of the INTEGRAL/SPI instrument response. This objective was successfully achieved. This analysis also highlights the presence of a significant instrumental background noise. Whereas, the second part concentrates on the data analysis of the Vela region observations. I have approached two astrophysical topics dealing with: - the search for radioactive decays lines of titanium-44, which is produced by explosive nucleosynthesis, in the supernova remnant of Vela Junior and, - the search of cyclotron resonance scattering features expected towards 25 keV and 52 keV in the accreting pulsar spectrum of the x-ray binary star Vela X-1. Putting forward the hypothesis that the result obtained previously by COMPTEL is correct and considering the no-detection of the titanium-44 lines by SPI, we give a lower limit at 4500 km s{sup -1} for the ejecta velocity from Vela Junior. The analysis on the research of the cyclotron lines have shown that the results are very sensitive to the instrumental background. Thorough studies will be necessary to guarantee an unambiguous detection of these lines. (author)

  12. Methodology of the 137 Cs for the soil erosion and deposition determination in a micro basin from the north of Parana State

    International Nuclear Information System (INIS)

    Andrello, Avacir Casanova

    1997-01-01

    The measurement of 137 Cs redistribution in the field allows the determination of soil erosion/accumulation. The 137 Cs activity of soil samples, taken from a small basin at the North of Parana, were measured employing a HPGe gamma ray detector and a standard spectrometric nuclear electronic chain. Standard oil samples with known concentrations of 137 Cs were prepared for the detection efficiency determination. Soil loss or gain was measured at the top, midslope and low slope regions, for six different transects at the investigated small basin. (author)

  13. Determination of the changes of antifungal properties of Satureja hortensis, Thymus vulgaris and Thymbra spicata exposed to gamma irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Gumus, Tuncay, E-mail: tgumus@nku.edu.t [Department of Food Engineering, Faculty of Agriculture, Namik Kemal University, Degirmenalti, 59030 Tekirdag (Turkey)

    2010-01-15

    In this research, changes in the antifungal activity of the extract of Satureja hortensis, Thymus vulgaris and Thymbra spicata exposed to gamma irradiation against two aflatoxigenic moulds Aspergillus parasiticus NRRL 2999 and 465 were investigated. The samples of dry plant leaf powder were irradiated with doses of 1.2, 3.0, 5.1 kGy. While the antifungal activity of S. hortensis with 0 and 1.2 kGy dose irradiation against A. parasiticus NRRL 2999 was found to be similar, it decreased with 3.0 and 5.1 kGy irradiation doses (P<0.05). On the contrary, antifungal activity of T. spicata increased until 3.0 kGy and then it decreased with 5.1 kGy irradiation dose (P<0.05). For T. vulgaris, an increase of irradiation dose resulted in a decrease of antifungal activity against aflatoxigenic moulds. This research shows that antifungal properties of some spices can be changed by gamma irradiation.

  14. Numerical bias estimation for mass spectrometric mass isotopomer analysis.

    Science.gov (United States)

    Yang, Tae Hoon; Bolten, Christoph J; Coppi, Maddalena V; Sun, Jun; Heinzle, Elmar

    2009-05-15

    Mass spectrometric (MS) isotopomer analysis has become a standard tool for investigating biological systems using stable isotopes. In particular, metabolic flux analysis uses mass isotopomers of metabolic products typically formed from (13)C-labeled substrates to quantitate intracellular pathway fluxes. In the current work, we describe a model-driven method of numerical bias estimation regarding MS isotopomer analysis. Correct bias estimation is crucial for measuring statistical qualities of measurements and obtaining reliable fluxes. The model we developed for bias estimation corrects a priori unknown systematic errors unique for each individual mass isotopomer peak. For validation, we carried out both computational simulations and experimental measurements. From stochastic simulations, it was observed that carbon mass isotopomer distributions and measurement noise can be determined much more precisely only if signals are corrected for possible systematic errors. By removing the estimated background signals, the residuals resulting from experimental measurement and model expectation became consistent with normality, experimental variability was reduced, and data consistency was improved. The method is useful for obtaining systematic error-free data from (13)C tracer experiments and can also be extended to other stable isotopes. As a result, the reliability of metabolic fluxes that are typically computed from mass isotopomer measurements is increased.

  15. Calibration of a Gamma Spectrometry System Used for the Determination of Cs-137 in Spanish Soils; Puesta a Punto de un sistema de Expectrometria Gamma para la Determinacion de Cs-137 en Suelos Espanoles

    Energy Technology Data Exchange (ETDEWEB)

    Barreraa, M.; Romero, M. L.; Valino, F.

    2008-07-01

    The document describes the methodology used at CIEMAT in order to determine, by gamma spectrometry, the background levels of the radionuclide Cs-137 in soils of the Spanish peninsular territory. the work is a part of an extensive research project developed jointly by the University of the Basque Country (UPV-EHU) and the CIEMAT, endellite Content and migration of radiocaesium and radiostrontium in Spanish soils, which is funded by the Plan I+D of the Spanish Nuclear Security Council (CSN). The objective of the project is to establish the reference levels of man-made radionuclides in Spanish soils, with respect to which the evaluation of a possible posterior accidental release of radioactive material could be appraised. The activity concentration of the fission products Cs-137 has been determined in 34 soil cores extracted from representative Spanish soils type zones. This publication describes the experimental system employed, its calibration, the particular conditions applied to perform the measurements, as well as the experimental validation of the methodology. The activity profiles and inventories of the radioactive element so obtained are also presented. The estimation of the background Cs-137 reference levels, will provide a basis for later applications as the study of the spatial distribution in the region, the determination of the correlation between the deposited activity and the meteorological conditions, or the calculation of the specific migration parameters of the radioactive elements in Mediterranean conditions. (Author) 15 refs.

  16. Plant trial of an under-belt capacitance and gamma-ray backscatter gauge for on-belt determination of moisture in coal

    International Nuclear Information System (INIS)

    Cutmore, N.G.; Rafter, P.T.; Abernethy, D.A.; Millen, M.J.

    1989-01-01

    A non-contacting under-belt capacitance and gamma-ray backscatter technique has been developed for the on-line measurement of moisture in coal. In this technique, moisture was correlated with radio frequency susceptance and conductance, determined using an under-belt capacitance sensor in which a fringing electric field interrogates a layer of coal on the conveyor belt directly about the sensor. To compensate for variations in the density and thickness of the coal layer, an under-belt gamma-ray backscatter gauge was used to measure an equivalent volume of coal. A plant trial of the technique was conducted at Stockton Borehole Colliery, NSW Australia, where the gauges were installed on the coking coal product conveyor. Product moistures, in the range 7-14%, were determined with r.m.s errors of 0.50 and 0.25 wt% using on-belt and static off-belt gauges, respectively. The difference in the on-belt and off-belt gauge measurement accuracy was attributed to sampling errors in the calibration of the on-belt gauge. 6 refs., 6 figs., 3 tabs

  17. {sup 129}I determination by direct Ge gamma-X spectrometry and its application to the concentration variation in two seaweed species

    Energy Technology Data Exchange (ETDEWEB)

    Barker, E.; Bouisset, P. [Institut de Radioprotection et de Surete Nucleaire (IRSN), Environmental Radioactivity Measurement Lab., 91 - Orsay (France); Masson, M.; Germain, P. [Institut de Radioprotection et de Surete Nucleaire (IRSN), Octeville-Cherbourg Radioecology Lab., 50 - Octeville -Cherbourg (France); Siclet, F. [Electricite de France (EDF), 78 - Chatou (France)

    2004-07-01

    The quantification of radionuclides by direct Ge gamma-X spectrometry with energy below 100 keV requires the elementary composition knowledge of the sample or the development of a device for determining the mass attenuation coefficients. This is especially true for {sup 129}I which is characterised by a 29.7 keV X-ray and 39.6 keV gamma ray. An experimental equipment has been developed in order to obtain this mass attenuation coefficient as a function of the energy. The elementary composition of a sample could change according to the biological phase of the organism and the sample preparation. {sup 129}I concentrations have been measured in samples of seaweed (Fucus serratus and Laminaria digitata) collected monthly during one year nearby La Hague reprocessing plant. Its quantification in different parts of these seaweeds was also performed in order to study the activity distribution. This paper will present measurement methodology used for {sup 129}I determination and its concentration variations during one-year period and the organo-tropism of {sup 129}I in the two seaweeds. (author)

  18. Rey: a computer code for the determination of the radionuclides activities from the gamma-ray spectrum data

    International Nuclear Information System (INIS)

    Palomares, J.; Perez, A.; Travesi, A.

    1978-01-01

    The Fortran IV computer Code, REY (REsolution and Identification), has been developed for the automatic resolution of the gamma-ray spectra from high resolution Ge-Li detectors. The Code searches the full energy peaks in the spectra background as the base line under the peak and calculates the energy of the statistically significant peaks. Also the Code assigns each peak to the most probable isotope and makes a selection of all the possible radioisotopes of the spectra, according the relative intensities of all the peaks in the whole spectra. Finally, it obtains the activities, in microcuries of each isotope, according the geometry used in the measurement. Although the Code is a general purpose one, their actual library of nuclear data is adapted for the analysis of liquid effluents from nuclear power plants. A computer with a 16 core memory and a hard disk are sufficient for this code.(author)

  19. Interaction of gamma radiation and temperature on the determination of the sterilizing dose of some stored products pests

    International Nuclear Information System (INIS)

    Barbosa, A.P.

    1976-08-01

    The influence of temperature on sterilizing dosages of gamma radiation was studied for Sitophilus zeamais Mots. in corn, Sitophilus oryzae (L.) in rice, Araecerus fasciculatus (DeGeer) in coffee, and Zabrotes subfasciatus (Boh.) in beans. It was found that temperature has a significant influence on the amount of radiation required to sterilize these species. The highest radiation dosages were required at those temperature most nearly optimum for insect development. The minimum radiation doses required for complete sterility of each species at the indicated temperatures were as follows: Sitophilus zeamais Mots. in corn, 8 krad at 24 0 C; Sitophilus oryzae (L.) in rice, 9 krad at 24 0 C; Araecerus fasciculatus (DeGeer) in coffee, 6 krad at 30 0 C; Zabrotes subfasciatus (Boh.) in beans, 9 krad at 24 - 27 0 C. At either higher or lower temperature smaller radiation dosages were required. (author) [pt

  20. Uncertainties in low {gamma}-dose determinations by means of ESR using the biomaterial modern coral reef

    Energy Technology Data Exchange (ETDEWEB)

    Hassan, Gamal M. [Department of Ionizing Radiation Metrology, National Institute for Standards (NIS), Tersa Street El-Haram El-Giza, P.O. Box 136 Giza, El-Giza (Egypt)]. E-mail: gamalhassan65@hotmail.com; Sharaf, M.A. [Department of Ionizing Radiation Metrology, National Institute for Standards (NIS), Tersa Street El-Haram El-Giza, P.O. Box 136 Giza, El-Giza (Egypt)

    2006-01-15

    The ESR spectrum of unirradiated modern aragonite coral (CaCO{sub 3}) material from the Red Sea (Hurgada area) is characterized by four signals with spectroscopic splitting factors of g=2.0056, 2.0030, 2.0006 and 1.997. The most intensive and stable line in this spectrum is attributed to CO{sub 2}{sup -} radicals at g=2.0006+/-0.0005. The dose response from 50mGy to 20Gy, energy dependence and effective atomic number are calculated so as to investigate coral as a dosimeter material in the clinical dose range. The lower experimental {gamma}-dose limit was found to be 50mGy with signal-to-noise (S/N) ratio of 15. The combined and expanded uncertainties accompanying these measurements are 1.72% and 3.44%, respectively.

  1. Determination of primordial and cosmogenic radioactivity in achondritic meteorites by low-level, gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Muntean, R.A.

    1979-08-01

    A high-sensitivity, low-background gamma-ray spectrometer containing two 23 cm by 13 cm thallium-activated, sodium iodide detectors was used to measure long-lived primordial and cosmogenic radioactivity in a suite of achondritic meteorites. Potassium, thorium, uranium, and 26 Al abundances were established for sixteen brecciated eucrites, two unbrecciated eucrites, a nakhlite, a chassignite, and a unique meteorite from Antarctica by nondestructive counting techniques. In several cases, multiple samples of the same meteorite fall were examined. Concentrations ranged from 79.8 ppM to 1150 ppM for potassium, 55.6 ppb to 663 ppb for thorium, 18.1 ppb to 190 ppb for uranium, and 45.0 dpm/kg to 99.0 dpm/kg for 26 Al. In addition, a 137 Cs concentration of 264 dpm/kg was observed in the Allan Hills 77005,9 specimen

  2. Application of gamma radiation backscattering in determining density and Zsub(eff) of scattering material Monte Carlo optimization of configuration

    International Nuclear Information System (INIS)

    Cechak, T.

    1982-01-01

    Applying Gardner's method of double evaluation one detector should be positioned such that its response should be independent of the material density and the second detector should be positioned so as to maximize changes in response due to density changes. The experimental scanning for optimal energy is extremely time demanding. A program was written based on the Monte Carlo method which solves the problem of error magnitude in case the computation of gamma radiation backscattering neglects multiply scattered photons, the problem of how this error depends on the atomic number of the scattering material as well as the problem of whether the representation of individual scatterings in the spectrum of backscattered photons depends on the positioning of the detector. 42 detectors, 8 types of material and 10 different density values were considered. The computed dependences are given graphically. (M.D.)

  3. Combining Internet monitoring processes, packaging and isotopic analyses to determine the market structure: example of Gamma Butyrolactone.

    Science.gov (United States)

    Pazos, Diego; Giannasi, Pauline; Rossy, Quentin; Esseiva, Pierre

    2013-07-10

    The Internet is becoming more and more popular among drug users. The use of websites and forums to obtain illicit drugs and relevant information about the means of consumption is a growing phenomenon mainly for new synthetic drugs. Gamma Butyrolactone (GBL), a chemical precursor of Gamma Hydroxy Butyric acid (GHB), is used as a "club drug" and also in drug facilitated sexual assaults. Its market takes place mainly on the Internet through online websites but the structure of the market remains unknown. This research aims to combine digital, physical and chemical information to help understand the distribution routes and the structure of the GBL market. Based on an Internet monitoring process, thirty-nine websites selling GBL, mainly in the Netherlands, were detected between January 2010 and December 2011. Seventeen websites were categorized into six groups based on digital traces (e.g. IP addresses and contact information). In parallel, twenty-five bulk GBL specimens were purchased from sixteen websites for packaging comparisons and carbon isotopic measurements. Packaging information showed a high correlation with digital data confirming the links previously established whereas chemical information revealed undetected links and provided complementary information. Indeed, while digital and packaging data give relevant information about the retailers, the supply routes and the distribution close to the consumer, the carbon isotopic data provides upstream information about the production level and in particular the synthesis pathways and the chemical precursors. A three-level structured market has been thereby identified with a production level mainly located in China and in Germany, an online distribution level mainly hosted in the Netherlands and the customers who order on the Internet. Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

  4. Spectrometric devices of itinerant radiometric laboratory

    International Nuclear Information System (INIS)

    Dolgirev, E.I.; Moroz, G.L.; Shchedrin, D.A.

    1978-01-01

    Scintillation gamma-spectrometer is described designed for mobile radiometric laboratory for individual monitoring of internal γ-radiation of members of the general population and service personnel as well as for analysis of the isotopic composition of radiocontaminants in the environment. Description and technical features of device are given. The detection unit consists of detectors made on the basis of NaI(Tl) monocrystals 63 x 63 mm in size. The unit permits measurement of various levels of gamma-emitting nuclides throughout the body and in the thyroid and lungs of man. Provision is made for measuring samples with high specific activities (more than 10 -5 Cu/g) and for examining individuals having high levels of incorporated radionuclides

  5. Determination of the neutron mass

    International Nuclear Information System (INIS)

    Amador V, P.; Chacon R, A.; Arcos P, A.; Rodriguez N, S.; Pinedo S, A.; Vega C, H.R.

    2005-01-01

    The binding energy of the deuteron was measured and it was determined the neutron mass starting from the nuclear reaction, 1 0 n + 1 1 H → 2 1 D + γ. The produced photon is soon a gamma ray that is emitted when the hydrogen captures a thermal neutron. The photon energy was measured using two spectrometric systems for gamma rays. A system with a detector of NaI(TI) of 3'' x 3'' and the other one with a High-purity Germanium detector. The first detector has a bigger efficiency and a smaller resolution in comparison with the second detector. The energy of the measured photon is the binding energy of the deuteron. With the measurement of the photon energy and the masses of the proton and of the deuterium it was determined the neutron mass. The value of the mass obtained with both systems it was compared with the value reported in the literature. The nuclear reaction was induced in a volume of paraffin that it was bombing with a source 239 PuBe whose activity is of 3.7 x 10 10 Bq. (Author)

  6. 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

  7. Identifying spectrometric signatures of phosphate deposits and enclosing sediments in Al-Awabed area, Northern Palmyrides, Central Syria, by the use of statistical factor analysis

    International Nuclear Information System (INIS)

    Asfahani, J.; Al-Hent, R.; Aissa, M.

    2007-01-01

    In previous published research, a factor analysis approach has been applied to airborne spectrometric data of Al-Awabed area, Northern Palmyrides, Syria. A model of four factors (F1, F2, F3 and F4) has proven to be sufficient to represent the acquired data, where 94% of the total data variance is explained. A powerful tool for direct differentiation of various rocks units is obtained through the mapping of these four factors, where a scored lithological map including 11 radiometric units is established. Ninety nine rock samples have been taken according to the four factors to be analyzed by the gamma spectrometry technique in order to determine their content of e U, e Th and K%. The analysis of 65 samples according to F1 indicates that uranium concentration varies between 2.74 and 123.3 ppm with an average of 58.85 ppm and a standard deviation of 32.53 ppm. The analysis of 18 samples taken according to F2 indicates that K% concentration varies between 0.001 and 0.324 with an average of 0.145 and a standard deviation of 0.122. The analysis of 16 samples taken according to F3 indicates that K% concentration varies between 0.024 and 0.558 with an average of 0.227 and a standard deviation of 0.133. These gamma-results are expected and fit very well with the results obtained by the factor analysis approach. Therefore, the validity and efficacy of the factor analysis approach, to be widely used as a guide in exploration and smart sampling for mining programs, are well demonstrated. The established phosphate maps show a width extension and distribution, and clearly indicate the potential of the research area, and it merits to be followed by economic exploration

  8. Mass Spectrometric Immunoassays in Characterization of Clinically Significant Proteoforms

    Directory of Open Access Journals (Sweden)

    Olgica Trenchevska

    2016-03-01

    Full Text Available Proteins can exist as multiple proteoforms in vivo, as a result of alternative splicing and single-nucleotide polymorphisms (SNPs, as well as posttranslational processing. To address their clinical significance in a context of diagnostic information, proteoforms require a more in-depth analysis. Mass spectrometric immunoassays (MSIA have been devised for studying structural diversity in human proteins. MSIA enables protein profiling in a simple and high-throughput manner, by combining the selectivity of targeted immunoassays, with the specificity of mass spectrometric detection. MSIA has been used for qualitative and quantitative analysis of single and multiple proteoforms, distinguishing between normal fluctuations and changes related to clinical conditions. This mini review offers an overview of the development and application of mass spectrometric immunoassays for clinical and population proteomics studies. Provided are examples of some recent developments, and also discussed are the trends and challenges in mass spectrometry-based immunoassays for the next-phase of clinical applications.

  9. Spectrometric electronic equipment for a 90-channel cherenkov mass spectrometer

    International Nuclear Information System (INIS)

    Astvatsaturov, R.G.; Basiladze, S.G.; Ivanov, V.I.

    1978-01-01

    Detecting spectrometric electronic equipment of a 90-channel cherenkov γ-spectrometer operating on-line with HP2116B type computer is described. The equipment contains linear amplifiers, analog memory blocks, a linear summator, discriminators, and a coincidence circuit. Three computer-controlled systems are used for checking the characteristics of the spectrometric electronic equipment, photomultipliers, and also for energy calibrations of the detectors. The long-term stability of the equipment has been measured with the aid of the checkup systems. It is established that the average instability of the pedestal magnitudes for all the channels is less than 10%, while the instability of the transmission coefficients is not worse than 0.5% for 5 days. The average nonlinearity over all the channels is 0.6%. The resolution time of the spectrometric equipment is 180 nsec

  10. Standard test methods for chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide (Gd2O3) powder

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2006-01-01

    1.1 These test methods cover procedures for the chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide powders to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Sections Carbon by Direct CombustionThermal Conductivity C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Total Chlorine and Fluorine by Pyrohydrolysis Ion Selective Electrode C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Loss of Weight on Ignition 7-13 Sulfur by CombustionIodometric Titration Impurity Elements by a Spark-Source Mass Spectrographic C761 Test Methods for Chemical, Mass Spectrometric, Spectrochemical,Nuclear, and Radiochemical Analysis of Uranium Hexafluoride C1287 Test Method for Determination of Impurities In Uranium Dioxide By Inductively Coupled Plasma Mass Spectrometry Gadolinium Content in Gadolinium Oxid...

  11. sup(99m)Tc-DTPA gamma-camera renography: Normal values and rapid determination of single-kidney glomerular filtration rate

    International Nuclear Information System (INIS)

    Rehling, M.; Moller, M.L.; Lund, J.O.; Trap-Jensen, J.; Jensen, K.B.; Thamdrup, B.

    1985-01-01

    A method for sup(99m)Tc-diethylenetriaminepentaacetate (DTPA) gamma-camera renography is presented. From each renogram an uptake index (UI) proportional to the single-kidney glomerular filtration rate (SKGFR) is defined. If the proportionality factor between UI and SKGFR is the same in all patients, UI can be used as an accurate measure of SKGFR. In order to test this, sup(99m)Tc-DTPA renography was performed in 101 patients with glomerular filtration rates (GFR) varying between 4 and 172 ml/min. The sum of the right- and left-kidney UIs correlated well with the total GFR calculated from the simultaneously measured plasma clearance of sup(99m)Tc-DTPA after a single injection. The correlation coefficient was 0.97. The method was tested in a prospective study of 57 patients. The total GFR estimated from the renograms was not significantly different from the GFR calculated from the plasma clearance of sup(99m)Tc-DTPA. The coefficient of variation -a combination of inaccuracy and imprecision in the estimates as well as in the reference values - was 11.8% at a GFR of 100 ml/min. It is concluded that, in adults, the SKGFR can be calculated as part of the clinical routine from sup(99m)Tc-DTPA gamma-camera renography without determining the injected dose or collecting urine or blood samples. Normal values for some parameters of the renogram obtained in 25 normal subjects are given. (orig.)

  12. Determination of 210Pb by direct gamma-ray spectrometry, beta counting via 210Bi and alpha-particle spectrometry via 210Po in coal, slag and ash samples from thermal power plant

    International Nuclear Information System (INIS)

    Seslak, Bojan; Vukanac, Ivana; Kandic, Aleksandar; Durasevic, Mirjana; Eric, Milic; Jevremovic, Aleksandar

    2017-01-01

    In order to compare three different techniques and estimate radiological impact, activity concentration of 210 Pb in coal, slag and ash samples from thermal power plant 'Nikola Tesla', Serbia, were measured, and results are presented in this study. Determination of 210 Pb was carried out in three ways: using HPGe gamma spectrometer and via in-growth of 210 Po and 210 Bi by alpha-particle spectrometry and proportional counting, respectively. The results obtained for three different techniques were compared. Statistical analysis and comparison of methods were carried out by combination of Z score and χ 2 statistical tests. Tests results, as well as values of measured activities concentrations obtained by alpha and gamma spectrometry, showed that gamma spectrometry is a valid alternative to time-consuming alpha spectrometry for low level activity measurements of 210 Pb. This remark is also valid even for gamma spectrometers with poor efficiency in low energy region. (author)

  13. Reliability of a 99sp(m)Tc-DTPA gamma camera technique for determination of single kidney glomerular filtration rate

    International Nuclear Information System (INIS)

    Rehling, M.; Moeller, M.L.; Thamdrup, B.; Lund, J.O.; Trap-Jensen, J.

    1986-01-01

    In a recent paper we described a method for calculation of single kidney glomerular filtration rate (SKGFR) from the 99 sp(m)Tc-DTPA renogram obtained by gamma camera. In this paper the reliability of the method was compared to other methods for estimation of GFR in 20 unilaterally nephrectomized patients. The values for SKGFR obtained from the renograms and from the estimated endogenous creatinine clearances according to serum creatinine concentration and a nomogram were both accurate. The reliability of the renography method was significantly better judged by less variance in the estimates. SKGFR calculated from the plasma clearance of 51 Cr-EDTA overestimated the renal clearance of inulin on an average by 11.3%. No difference was found in the variance of the values obtained from the renograms and from the plasma clearances of 51 Cr-EDTA compared to the renal clearance of inulin. Apart from the inaccuracy in the GFR values calculated from the plasma clearance of 51 Cr-EDTA, the reliability of these two methods was equal. (author)

  14. Determination of radio nuclides for some local foodstuffs in Republic of Yemen by using gamma rays spectral analysis technique

    International Nuclear Information System (INIS)

    Al-Maqtary, K.; Murshid, M.; Bazohair, A.; Al-Zuhairy, M.

    2008-01-01

    This study is considered as the first research study on locally produced consumed food in the Republic of Yemen. The objective of this study is to measure concentration of radio nuclides 137 Cs and 40 K In food samples produced in Yemen. Twenty two local foodstuffs samples were collected from provinces. The mar IBB, Hudiadah and Lahj, due to the massive crops production. Gamma spectroscopy consist of high purity germanium (HPGe) detector with resolution of 2.11 KeV at 1332 ke v energy which related to 6 0Co isotope. The detector is interfaced to two amplifiers and multichannel analyzer (mca). the maximum concentration of 13C s was found in garden pea samples brought from Lahj province 13± 1.5 Bq/kg. The minimum concentration was found in wheat samples brought from Them ar province 2.5± 0.2 Bq/Kg. The maximum concentration of 4 0K was found in garden pea samples brought from Lahj. 1000±15 Bq/kg. The minimum concentration was in forage sorghum samples brought from Hudaidah 40±1.5 Bq/kg. The studies samples are radiological safe and okay for human consumption. (author)

  15. Determination of gamma radiation dose to the destruction of Escherichia coli O157: H7 in hamburger

    International Nuclear Information System (INIS)

    Orejuela Chirinos, Rodolfo Raul

    1999-01-01

    Escherichia coli O157:H7 has been incriminated in several foodborne outbreaks due to the consumption of different kinds of foods. Among these, hamburgers are the most common. Irradiation process is an effective method for food preservation because it causes no significant change in organoleptic and nutritional food characteristics and destroys pathogens and spoilage microorganisms. Hamburgers and nutrient broth inoculated with Escherichia coli O157:H7 were submitted to gamma irradiation ( 60 Co) treatment, with doses ranging from 0,0 to 0,7 kGy in order to calculate the D 10 for this bacteria in these substrate. The D 10 for the pathogen nutrient broth ranged from 0.08 kGy to 0.10 kGy and in hamburger from 0.11 kGy to 0.21 kGy. Considering the highest D 10 value in hamburger, a dose of 0,8 kGy would not change the sensorial characteristics of the product, and would reduce the population of E. coli O157:H7 in 4 cycles logarithmic. (author)

  16. Determination dimension and technical specification of the cylindrical pneumatics for the tote movement on multipurpose the gamma irradiator BATAN

    International Nuclear Information System (INIS)

    Muhammad Subhan; Ari Satmoko

    2016-01-01

    BATAN develops irradiator gamma category IV in cooperation with IZOTOP (Hungary). Transportation technology products that will be developed uses rail system to pool. Products that will be irradiated are put into tote then placed on the transportation rail, when tote has been in irradiated room tote enters into irradiated rack. The movement of the tote during on irradiated rack will be driven by the pneumatic system. Based on data from Isotop there are 14 cylindrical pneumatics that are in the irradiated room. Through the results analysis then used double acting cylinder type from the Festo pneumatics catalog. Through the results calculation that the force used on all types of cylinders for movement tote still much smaller than of force bent permitted. Beside that there are 4 group a pneumatic have common specifications they are group one cylindrical C1, C3, C12 and C14 they are group two cylindrical C2, C4, C11, and C13 they are group three cylindrical C7, C9, C15 and C17 they are group four cylindrical C10 and C17. (author)

  17. Determination of curie content and 134/137cesium ratios by gamma spectroscopy of high burnup plutonium-aluminum fuel assemblies

    International Nuclear Information System (INIS)

    Haggard, D.L.; Tanner, J.E.

    1997-06-01

    Nondestructive assay (NDA) gamma spectroscopy techniques were used to measure 134/137 Cs ratios on nine PuAl Mark 42 fuel assemblies. The purpose of the ratio measurement was to confirm theoretical burnup calculations. 134/137 Cs ratios were determined from the measured activity based on corrected net peak area counts for the 605 keV peak from 134 Cs and the 662 keV peak from 137 Cs/ 137m Ba. Assembly No. 2 134/137 Cs ratio measured on 4-15-92 was 0.19. The measured 134/137 Cs ratio was decay corrected to be 2.11 on 8-1-84 based on the half lives of 134 Cs and 137 Cs. The measured 134/137 Cs ratio range was 1.90--2.14 for all nine assemblies. These measured values compare to a theoretical ratio of 1.7 on 8-1-84 determined by burnup calculations. Total cesium curie content was also requested and determined using the NDA direct measurements. Gamma spectral data were measured on the nine sectioned Mark 42 fuel assemblies. Measured cesium curie content, decay corrected to 8-1-84, ranged from 18170--24480 curies of 134 Cs and 8620--11646 curies of 137 Cs. Theoretical cesium curie content of 8-1-84 was 15200 curies 134 Cs and 8973 curies 137 Cs. Direct assay cesium ratio is 12% to 26% higher than the predicted ratio of 1.7. The measured 134 Cs data indicate between 20%--61% more activity than that predicted by the burnup code, whereas the measured 137 Cs activity is between 4% less to 30% more than the predicted activity. This information may be used to address issues concerning criticality safety, storage, and shipping of this type of material

  18. Determination of curie content and {sup 134/137}cesium ratios by gamma spectroscopy of high burnup plutonium-aluminum fuel assemblies

    Energy Technology Data Exchange (ETDEWEB)

    Haggard, D.L.; Tanner, J.E.

    1997-06-01

    Nondestructive assay (NDA) gamma spectroscopy techniques were used to measure {sup 134/137}Cs ratios on nine PuAl Mark 42 fuel assemblies. The purpose of the ratio measurement was to confirm theoretical burnup calculations. {sup 134/137}Cs ratios were determined from the measured activity based on corrected net peak area counts for the 605 keV peak from {sup 134}Cs and the 662 keV peak from {sup 137}Cs/{sup 137m}Ba. Assembly No. 2 {sup 134/137}Cs ratio measured on 4-15-92 was 0.19. The measured {sup 134/137}Cs ratio was decay corrected to be 2.11 on 8-1-84 based on the half lives of {sup 134}Cs and {sup 137}Cs. The measured {sup 134/137}Cs ratio range was 1.90--2.14 for all nine assemblies. These measured values compare to a theoretical ratio of 1.7 on 8-1-84 determined by burnup calculations. Total cesium curie content was also requested and determined using the NDA direct measurements. Gamma spectral data were measured on the nine sectioned Mark 42 fuel assemblies. Measured cesium curie content, decay corrected to 8-1-84, ranged from 18170--24480 curies of {sup 134}Cs and 8620--11646 curies of {sup 137}Cs. Theoretical cesium curie content of 8-1-84 was 15200 curies {sup 134}Cs and 8973 curies {sup 137}Cs. Direct assay cesium ratio is 12% to 26% higher than the predicted ratio of 1.7. The measured {sup 134}Cs data indicate between 20%--61% more activity than that predicted by the burnup code, whereas the measured {sup 137}Cs activity is between 4% less to 30% more than the predicted activity. This information may be used to address issues concerning criticality safety, storage, and shipping of this type of material.

  19. International comparison of interpolation procedures for the efficiency of germanium gamma-ray spectrometers (GAM83 exercise)

    International Nuclear Information System (INIS)

    Zijp, W.L.; Polle, A.N.; Nolthenius, H.J.

    1986-01-01

    Results are presented for the outcome of an international intercomparison of a particular gamma-ray spectrometric procedure. Laboratories were asked to determine full energy peak efficiencies and activities by means of their own procedures, starting from supplied peak-efficiency data. Four data sets for four different conditions of germanium detectors were distributed. The sets comprised: a high accuracy- (uncertainty > 1%) data set with a relatively large number of measured data (SET 1); a low accuracy- (uncertainty 3-5%) data set with a relatively small number of measured data (SET 2); a low energy-data set (SET 3); a high accuracy-data set with a relatively small number of measured data (SET 4). The intercomparison (coded GAM83) was organized and analyzed under auspices of the International Committee for Radionuclide Metrology (ICRM). The results comprise the analysis of the contributions of 41 participants

  20. 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)