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Sample records for 238u funktsii vozbuzhdeniya

  1. Study on the formation of the composite system of 238U+238U

    Institute of Scientific and Technical Information of China (English)

    WU Xi-Zhen; TIAN Jun-Long; ZHAO Kai; ZHANG Ying-Xun; LI Zhu-Xia

    2009-01-01

    Strongly damped reactions of 238U+238U, at Ecm = 680-1880 MeV have been studied based on the improved quantum molecular dynamics model. We find that at a certain energy region the entrance channel potential is weakly repulsive and the dissipation is very strong after touching configuration, these two effects make the time delay of re-separation for colliding system. The single particle potential well of the transiently formed composite system has Coulomb barrier about 15-20 MeV high at the surface, which makes the excited unbound protons being still embedded in the potential well and moving in a common mono-single particle potential for a period of time and thus restrains from quick decay of the composite system.

  2. Electron scattering from the octupole band in /sup 238/U

    Energy Technology Data Exchange (ETDEWEB)

    Hirsch, A.; Creswell, C.; Bertozzi, W.; Heisenberg, J.; Hynes, M.V.; Kowalski, S.; Miska, H.; Norum, B.; Rad, F.N.; Sargent, C.P.; Sasanuma, T.; Turchinetz, W.

    1978-03-06

    A simple model for nuclear surface vibrations in permanently deformed nuclei does well in reproducing electron scattering cross sections of rotational levels built on a K/sup ..pi../= 0/sup -/ intrinsic octupole vibration in /sup 238/U.

  3. Electric and Magnetic Dipole States in ^238U

    Science.gov (United States)

    Hammond, S. L.; Adekola, A.; Angell, C. T.; Karwowski, H. J.; Howell, C. R.; Kwan, E.; Rusev, G.; Tonchev, A. P.; Tornow, W.; Kelley, J. H.

    2010-11-01

    An investigation of dipole states in ^238U is important for the fundamental understanding of its structure. Precise experimental information on the distribution of M1 and E1 transitions in ^238U has been obtained using the nuclear resonance fluorescence technique at the High-Intensity γ-ray Source at the Triangle Universities Nuclear Laboratory. Using 100% linearly-polarized, monoenergetic γ-ray beams between incident energies of 2.0 - 5.5 MeV, the spin, parity, width, and γ-strength of the ground-state deexcitations were determined. These measurements will form a unique data set that can be used for comparison with theoretical models of collective excitations in heavy, deformed nuclei. The data can also provide isotope-specific signatures to search for special nuclear materials.

  4. Phosphate fertilizer influence on {sup 238} U content in vegetables

    Energy Technology Data Exchange (ETDEWEB)

    Lauria D, C.; Rodrigues S, J.I. [Instituto de Radioprotecao e Dosimetria (IRD/CNEN), Av. Salvador Allende s/n, Rio de Janeiro-RJ (Brazil); Ribeiro, F.C.A. [Centro Regional de Ciencias Nucleares (CRCN/CNEN) Av. Prof. Luiz Freire 200 Cidade Universitaria Recife-PE (Brazil)]. e-mail: dejanira@ird.gov.br

    2006-07-01

    Uranium is a naturally radioactive element, which is usually found in soils, superficial and ground water, vegetables and animals. After ingestion by human beings, most is excreted in few days by feces and urine, without reaching the bloodstream. However, a small part circulates through the body, being accumulated in the soft tissues, as kidneys. A minor fraction can remain in bones per some years, being able through the radioactive decay to irradiate adjacent tissues. Phosphate fertilizers used in conventional crop management can present variable amounts of uranium. In accordance with origin and use, the fertilizer can raise the content of this element in vegetables, and consequently to increase the human exposure for radiation due the consumption of vegetables. It is estimated that the use of phosphate fertilizer has at least doubled the prolonged exposure of humans from ingestion of food. This work aims to evaluate the contribution of organic and chemical fertilizer on the concentration of {sup 238} U in vegetable samples. An experiment with black beans (a very important vegetable for Brazilian people) was conducted in a field which soil has never been fertilized with any sort of fertilizer, located near to the Rio de Janeiro city. On the organic management, bovine manure was used, while on conventional management urea, potassium chloride and superphosphate were used. Simultaneously, black bean samples from not fertilized management were collected. In addition, lettuce and carrot samples from organic and conventional managements were collected in Nova Friburgo farms (the most important vegetable supplier of Rio de Janeiro city market). The analyses of {sup 238} U have been carried out by conventional fluorimetric method. The geometric mean of {sup 238} U concentrations in the carrot and lettuce samples from conventional management were similar with those from organic management, while for beans the conventional samples had higher values than those ones found in

  5. Synthesis of superheavy nuclei with 238U target

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The production of superheavy nuclei with Z=108-116 via hot fusion reactions of the neutron-rich projectiles with 238U target is systematically studied.The results show that the production cross sections of superheavy nuclei do not decrease monotonously as the atomic number Z increasing.The cross sections of the superheavy nuclei at Z = 112 and 115 are enhanced as compared with the whole Z-trend in synthesis of the superheavy nuclei,which clearly illustrates that the reactions with large negative Q-value and shell correction are more favorable to synthesize superheavy nuclei.

  6. Synthesis of superheavy nuclei with 238U target

    Institute of Scientific and Technical Information of China (English)

    LIU ZuHua; BAO JingDong

    2009-01-01

    The production of superheavy nuclei with Z=108-116 via hot fusion reactions of the neutron-rich projectiles with 238u target is systematically studied.The results show that the production cross sections of superheavy nuclei do not decrease monotonously as the atomic number Z increasing.The cross sections of the superheavy nuclei at Z=112 and 115 are enhanced as compared with the whole Z-trend in synthesis of the superheavy nuclei,which clearly illustrates that the reactions with large negative Q-value and shell correction are more favorable to synthesize superheavy nuclei.

  7. The production of unknown neutron-rich isotopes in $^{238}$U+$^{238}$U collisions at near-barrier energy

    CERN Document Server

    Zhao, Kai; Zhang, Yingxun; Wang, Ning; Li, Qingfeng; Shen, Caiwan; Wang, Yongjia; Wu, Xizhen

    2016-01-01

    The production cross sections for primary and residual fragments with charge number from $Z$=70 to 120 produced in the collision of $^{238}$U+$^{238}$U at 7.0 MeV/nucleon are calculated by the improved quantum molecular dynamics (ImQMD) model incorporated with the statistical evaporation model (HIVAP code). The calculation results predict that about sixty unknown neutron-rich isotopes from element Ra ($Z$=88) to Db ($Z$=105) can be produced with the production cross sections above the lower bound of $10^{-8}$ mb in this reaction. And almost all of unknown neutron-rich isotopes are emitted at the laboratory angles $\\theta_{lab}\\leq$ 60$^\\circ$. Two cases, i.e. the production of the unknown uranium isotopes with $A\\geq$ 244 and that of rutherfordium with $A\\geq$ 269 are investigated for understanding the production mechanism of unknown neutron-rich isotopes. It is found that for the former case the collision time between two uranium nuclei is shorter and the primary fragments producing the residues have smaller...

  8. Neutron Induced Capture and Fission Processes on 238U

    Directory of Open Access Journals (Sweden)

    Oprea Cristiana

    2016-01-01

    Full Text Available Nuclear data on Uranium isotopes are of crucial interest for new generation of nuclear reactors. Processes of interest are the nuclear reactions induced by neutrons and in this work mainly the capture and the fission process on 238U will be analyzed in a wide energy interval. For slow and resonant neutrons the many levels Breit – Wigner formalism is necessary. In the case of fast and very fast neutrons up to 200 MeV the nuclear reaction mechanism implemented in Talys will be used. The present evaluations are necessary in order to obtain the field of neutrons in the design of nuclear reactors and they are compared with experimental data from literature obtained from capture and (n,xn processes.

  9. Dose effect for South Serbians due to {sup 238}U in natural drinking water

    Energy Technology Data Exchange (ETDEWEB)

    Sahoo, S.K.; Matsumoto, M.; Shiraishi, K.; Fujimoto, K. [Department of Radiation Dosimetry, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan); Cuknic, O.; Zunic, Z.S. [Institute of Nuclear Sciences, VINCA, PO Box 522, 11001 Belgrade (Serbia)

    2007-07-01

    The use of depleted uranium ammunition in South Serbia during the 1999 Kosovo conflict raised a great deal of public concern in the Balkans. Radioactivity levels of {sup 238}U in 20 wells and lake water samples were checked from the viewpoint of internal radiation exposure for South Serbian subjects. We have measured {sup 238}U concentration using inductively coupled plasma mass spectrometry, whereas thermal ionisation mass spectrometry has been used for the measurement of isotope ratios, e.g. {sup 234}U/{sup 238}U and {sup 235}U/{sup 238}U. The concentration of uranium in water samples varies in the range 1.37-63.18 mBq/L. {sup 234}U belongs to the {sup 238}U natural radioactive decay series, and at secular equilibrium, the abundance ratio, {sup 234}U/{sup 238}U, corresponds to the ratio of their half-lives. The {sup 234}U/{sup 238}U activity ratio varies in the range 0.88-2.2 and {sup 235}U/{sup 238}U isotope ratio varies from 0.00698 to 0.00745. These findings indicate that uranium in water was a mixture of natural and anthropogenic origin. The annual effective dose due to {sup 238}U was estimated to be in the range 9.2 x 10{sup -5} - 2.1 x 10{sup -3} mSv. (authors)

  10. Studying Nuclear Level Densities of 238U in the Nuclear Reactions within the Macroscopic Nuclear Models

    Science.gov (United States)

    Razavi, Rohallah; Rahmatinejad, Azam; Kakavand, Tayeb; Taheri, Fariba; Aghajani, Maghsood; Khooy, Asghar

    2016-02-01

    In this work the nuclear level density parameters of 238U have been extracted in the back-shifted Fermi gas model (BSFGM), as well as the constant temperature model (CTM), through fitting with the recent experimental data on nuclear level densities measured by the Oslo group. The excitation functions for 238U(p,2nα)233Pa, and 238U(p,4n)235Np reactions and the fragment yields for the fragments of the 238U(p,f) reaction have been calculated using obtained level density parameters. The results are compared to their corresponding experimental values. It was found that the extracted excitation functions and the fragment yields in the CTM coincide well with the experimental values in the low-energy region. This finding is according to the claim made by the Oslo group that the extracted level densities of 238U show a constant temperature behaviour.

  11. Prospects of heavy and superheavy element production via inelastic nucleus-nucleus collisions - from 238U+238U to18O+254Es

    Science.gov (United States)

    Schädel, Matthias

    2016-12-01

    Multi-nucleon transfer reactions, frequently termed deep-inelastic, between heavy-ion projectiles and actinide targets provide prospects to synthesize unknown isotopes of heavy actinides and superheavy elements with neutron numbers beyond present limits. The 238U on 238U reaction, which revealed essential aspects of those nuclear reactions leading to surviving heavy nuclides, mainly produced in 3n and 4n evaporation channels, is discussed in detail. Positions and widths of isotope distributions are compared. It is shown, as a general rule, that cross sections peak at irradiation energies about 10% above the Coulomb barrier. Heavy target nuclei are essential for maximizing cross sections. Experimental results from the 238U on 248Cm reaction, including empirical extrapolations, are compared with theoretical model calculations predicting relatively high cross sections for neutron-rich nuclei. Experiments to test the validity of such predictions are proposed. Comparisons between rather symmetric heavy-ion reactions like 238U on 248Cm (or heavier targets up to 254Es) with very asymmetric ones like 18O on 254Es reveal that the ones with 238U as a projectile have the highest potential in the superheavy element region while the latter ones can be advantageous for the synthesis of heavy actinide isotopes. Concepts for highly efficient recoil separators designed for transfer products are presented.

  12. Experimental Determination of the Antineutrino Spectrum of the Fission Products of $^{238}$U

    CERN Document Server

    Haag, N; Hofmann, M; Oberauer, L; Potzel, W; Schreckenbach, K; Wagner, F M

    2013-01-01

    An experiment was performed at the scientific neutron source FRM II in Garching to determine the cumulative antineutrino spectrum of the fission products of $^{238}$U. This was achieved by irradiating target foils of natural uranium with a thermal and a fast neutron beam and recording the emitted $\\beta$-spectra with a gamma-suppressing electron-telescope. The obtained $\\beta$-spectrum of the fission products of $^{235}$U was normalized to the data of the magnetic spectrometer BILL of $^{235}$U. This method strongly reduces systematic errors in the $^{238}$U measurement. The $\\beta$-spectrum of $^{238}$U was converted into the corresponding antineutrino spectrum. The final $\\bar\

  13. Neutron and fission yields from high-energy deuterons in infinite /sup 238/U targets

    Energy Technology Data Exchange (ETDEWEB)

    Canfield, E.

    1965-06-28

    Early work on the interaction of high energy deuterons with large /sup 238/U targets is reexamined and current theoretical study is discussed. Results of fission and neutron yield calculations are compared with experiment. (SDF)

  14. Experimental determination of the antineutrino spectrum of the fission products of {sup 238}U

    Energy Technology Data Exchange (ETDEWEB)

    Haag, Nils-Holger

    2013-10-09

    Fission of {sup 238}U contributes about 10 % to the antineutrino emission of a pressurized water reactor. In the present thesis, the beta spectrum of the fission products of {sup 238}U was determined in an experiment at the neutron source FRM II. This beta spectrum was subsequently converted into an antineutrino spectrum. This first measurement of the antineutrino spectrum supports all current and future reactor antineutrino experiments.

  15. (234)U/(238)U signatures associated with uranium ore bodies: part 1 Ranger 3.

    Science.gov (United States)

    Lowson, Richard T; McIntyre, Mark G

    2013-04-01

    The Ranger 3 ore body is an early Proterozoic U ore body in the Alligator Rivers U province, Northern Territory, Australia. It has surface expression with a redox front located between 30 and 50 m below the surface. The ground water U concentration and (234)U/(238)U AR signature in the top 10 m of the weathered zone are reported for 357 samples collected over 4 wet seasons, at 5 depths, along a transect in-line with the hydraulic gradient and along the centre line of the ore body and its associated dispersion halo. The results show that the weathered zone displays a general U isotope feature for this type of ore body with the (234)U/(238)U AR for the ground water and amorphous phase of the solid matrix being less than 1. The ground water (234)U/(238)U AR is independent of the annual monsoonal climate and depth within the range surface to 10 m. In the vicinity of the U ore body the ground water (234)U/(238)U AR is 0.75 and is very similar to the (234)U/(238)U AR of the amorphous phase of the solid (0.76). The (234)U/(238)U ARs of the amorphous phase and ground water rise and separate to values of 0.88 and 1.02 at the end of the transect. The rise and separation in (234)U/(238)U AR are interpreted as evidence that the source of the U in the ground water is from the water-soluble sub-phase of the amorphous phase and that the ground water flow is too fast to allow the processes occurring across the solid-water interface to reach chemical equilibrium. The data set is a robust characterisation of the coarse and fine detail of the (234)U/(238)U AR signature in the weathered zone of U ore bodies.

  16. Study for fusion-fission and quasifission in reactions using {sup 238}U target nucleus

    Energy Technology Data Exchange (ETDEWEB)

    Nishio, Katsuhisa, E-mail: nishio.katsuhisa@jaea.go.jp [Advanced Science Reserch Center, Japan Atomic Energy Agency, Tokai, Ibraki 319-1195 (Japan)

    2011-02-01

    Fragment mass distributions for fission after full momentum transfer (FMT) were measured for the {sup 30}Si,{sup 31}P,{sup 34,36}S,{sup 40}Ar + {sup 238}U reactions at bombarding energies around the Coulomb barrier. The experiment was carried out at the JAEA tandem accelerator facility. We observed strong variation of the mass distribution on beam energy and projectile nucleus. In the reaction of {sup 36}S +{sup 238}U we observed a transition from symmetry to asymmetry mass distributions when the beam energies were decreased from the above-barrier to sub-barrier values. The mass asymmetry was A{sub L} /A{sub H} = 74/200, which corresponds to the fission valley leading to the nuclei close to the doubly closed-shell nuclei {sup 78}Ni /{sup 208}Pb. The fission channel is populated by quasifission, which is the disintegration without forming the compound nucleus. The incident-energy dependence is strongly correlated with the prolate deformation of {sup 238}U and the orientation at the initial impact. The results indicate that the reaction starting at the polar collisions on {sup 238}U has larger quasifission probability. The mass distributions are nicely reproduced by a model calculation using Langevin equation. The {sup 40}Ar + {sup 238}U reaction also has the similar mass asymmetry (A{sub L}/A{sub H} {approx} 78/200) in quasifission. In the reactions of {sup 31}P + {sup 238}U and {sup 30}Si + {sup 238}U, mass asymmetries are A{sub L}/A{sub H} 81/188 and 90/178, respectively. The results suggest that the system produced by the reaction using lighter projectile approaches closer to the shape of the compound nucleus even when quasifission occurs. In the reactions of {sup 30}Si +{sup 238}U and {sup 34}S+ {sup 238}U, we also measured the evaporation residue (ER) cross sections to obtain information on the fusion probability. From the ER cross sections for the {sup 34}S+{sup 238}U reaction it was suggested that the symmetric fission is also dominated by quasifission.

  17. The Application of 238U/235U as a Redox-Proxy for Past Ocean Chemistry

    Science.gov (United States)

    Andersen, M. B.; Westermann, S.; Bahniuk, A.; Vasconcelos, C.; McKenzie, J. A.; Föllmi, K. B.; Vance, D.

    2014-12-01

    The recent discovery of significant variation in 238U/235U caused by redox change at the surface Earth has led to its use to extract information on the oxygenation state of ancient oceans from marine sediments [e.g. 1]. Recent studies have focused on improving the understanding of the 238U/235U signature in modern marine carbonates [2] and black shales [3] to improve the robustness of this tracer. To further advance its use we have focused on improving our understanding of 238U/235U systematics in modern dolomite, another commonly occurring rock-type in the geological record, before turning to 238U/235U signatures in ancient sediments. The measured dolomite samples, precipitated in modern environments of coastal hypersaline lagoons in Brazil, all exhibit 238U/235U values that deviate from the seawater composition [3]. Observed values are both lighter (ca. 130 ppm; as also observed in dolomite from tidal-ponds on Bahamas [2]) and heavier (50-180 ppm). These distinct 238U/235U values for different dolomite-precipitates likely attest to the particular formation style, as well as early diagenetic processes. We use such modern settings to discuss the utility of 238U/235U in ancient sediments, the singularity of any observed 238U/235U signal, its relation to global ocean chemistry and potential diagenetic overprinting. These constraints are then used to evaluate a well-preserved marine carbonate section [4] and published black shale 238U/235U data [1], both deposited during the Oceanic Anoxic Event 2 (93 Ma). We discuss the capabilities of both the carbonate and black shale section for retaining information on the 238U/235U composition in the ocean during OAE 2. [1] Montoya-Pino et al. (2010) Geology, 38, 315-318 [2] Romaniello et al. (2013) 362, 305-316 [3] Andersen et al. (2014) EPSL, 400, 184-194 [4] Westermann et al. (2010) Cret. Res., 31, 500-514

  18. (234)U/(238)U signatures associated with uranium ore bodies: part 3 Koongarra.

    Science.gov (United States)

    Lowson, Richard T

    2013-04-01

    The Koongarra ore body is an early Proterozoic U ore body in the Alligator Rivers U province, Northern Territory, Australia. It has surface expression with a redox front located ∼30 m below the surface. The (234)U/(238)U activity ratios (AR) for the ground water and the amorphous phase of the solid have been analysed for the ore zone and dispersion halo as a function of depth. The results display a (234)U/(238)U AR signature with depth which may be common to all U ore bodies. The (234)U/(238)U AR is depressed below secular equilibrium in the weathered material above the redox front; rises significantly above secular equilibrium in the vicinity of the redox front; and is followed by a gradual decrease with depth below the redox front. The amplitude of the profile is a function of local conditions. A model is proposed for the signature in which oxidising waters preferentially leach the (234)U sites at the redox front due to preconditioning of the (234)U sites by α recoil during the decay of (23)(8)U to (23)(4)U. Mass balance requires the solid material left behind the redox front to have a (234)U/(238)U AR reduced below 1. Local second order effects may be superimposed on the signature. The signature may have application to calibrating scenarios for nuclear waste repositories, assisting in understanding historical climates, economic evaluation of U ore bodies and U exploration.

  19. Transmission Nuclear Resonance Fluorescence Measurements of 238U in Thick Targets

    Energy Technology Data Exchange (ETDEWEB)

    Quiter, Brian J.; Ludewigt, Bernhard A.; Mozin, Vladimir V.; Wilson, Cody; Korbly, Steve

    2010-08-31

    Transmission nuclear resonance fluorescence measurements were made on targets consisting of Pb and depleted U with total areal densities near 86 g/cm2. The 238U content n the targets varied from 0 to 8.5percent (atom fraction). The experiment demonstrates the capability of using transmission measurements as a non-destructive technique to identify and quantify the presence of an isotope in samples with thicknesses comparable to he average thickness of a nuclear fuel assembly. The experimental data also appear to demonstrate the process of notch refilling with a predictable intensity. Comparison of measured spectra to previous backscatter 238U measurements indicates general agreement in observed excited states. Two new 238U excited states and possibly a third state have also been observed.

  20. Recent measurements of 234U/238U isotope ratio in spring waters from the Hadzici area.

    Science.gov (United States)

    Vidic, Alfred; Ilić, Zorana; Benedik, Ljudmila

    2013-06-01

    The Hadzici area has become interesting for investigation since depleted uranium ammunition had been employed in 1995 during the NATO air strike campaign in Bosnia and Herzegovina. The purpose of this study is to determine uranium concentration and (234)U/(238)U activity ratio in the spring waters of this area and to investigate their relationship, as well as spatial variations. The spring water samples were taken at 18 sites in total. For the determination of uranium radioisotopes, radiochemical separation procedure followed by alpha-particle spectrometry was applied. Uranium concentration in analyzed waters range from 0.15 to 1.12 μg/L. Spring waters from carbonate based sediments have a lower uranium concentration of between 0.15 and 0.43 μg/L, in comparison to waters sampled within sandstone-based sediments ranging from 0.53 to 1.12 μg/L. Dissolved uranium shows significant spatial variability and correlation with bedrock type confirmed by Principal Component Analysis and Hierarchical Cluster Analysis. The majority of the analyzed waters have a (234)U/(238)U activity ratio ranging from 1.02 to 1.90, of which half of the results range between 1.02 and 1.16. No apparent depleted uranium (DU) contamination was observed, as (234)U/(238)U activity ratio is dependent on geochemical conditions in the environment. Even though the tested spring waters demonstrate significant variability in uranium concentration, (234)U/(238)U activity ratio and (234)U excess, waters with similar uranium isotopic signatures are observable within the region. The guidelines on the spatial redistribution of dissolved uranium (corresponding to (238)U mass concentration), along with (234)U/(238)U activity ratios were provided by the Inverse Distance Weighting (IDW) method. Waters having similar isotopic signature have been delineated.

  1. Determination of the isotopic ratio {sup 234} U/{sup 238} U and {sup 235} U/{sup 238} U in uranium commercial reagents by alpha spectroscopy; Determinacion de la relacion isotopica {sup 234} U/{sup 238} U y {sup 235} U/{sup 238} U en reactivos comerciales de uranio por espectrometria alfa

    Energy Technology Data Exchange (ETDEWEB)

    Iturbe G, J.L

    1990-02-15

    In this work the determination of the isotope ratio {sup 234} U/{sup 238} U and {sup 235} U/{sup 238} U obtained by means of the alpha spectroscopy technique in uranium reagents of commercial marks is presented. The analyzed uranium reagents were: UO{sub 2} (*) nuclear purity, UO{sub 3} (*) poly-science, metallic uranium, uranyl nitrate and uranyl acetate Merck, uranyl acetate and uranyl nitrate Baker, uranyl nitrate (*) of the Refinement and Conversion Department of the ININ, uranyl acetate (*) Medi-Lab Sigma of Mexico and uranyl nitrate Em Science. The obtained results show that the reagents that are suitable with asterisk (*) are in radioactive balance among the one {sup 234} U/{sup 238} U, since the obtained value went near to the unit. In the case of the isotope ratio {sup 235} U/{sup 238} U the near value was also obtained the one that marks the literature that is to say 0.04347, what indicates that these reagents contain the isotope of {sup 235} U in the percentage found in the nature of 0.71%. The other reagents are in radioactive imbalance among the {sup 234} U/{sup 238} U, the found values fluctuated between 0.4187 and 0.1677, and for the quotient of activities {sup 235} U/{sup 238} U its were of 0.0226, and the lowest of 0.01084. Also in these reagents it was at the {sup 236} U as impurity. The isotope of {sup 236} U is an isotope produced artificially, for what is supposed that the reagents that are in radioactive imbalance were synthesized starting from irradiated fuel. (Author)

  2. Ocean mixing and ice-sheet control of seawater 234U/238U during the last deglaciation

    Science.gov (United States)

    Chen, Tianyu; Robinson, Laura F.; Beasley, Matthew P.; Claxton, Louis M.; Andersen, Morten B.; Gregoire, Lauren J.; Wadham, Jemma; Fornari, Daniel J.; Harpp, Karen S.

    2016-11-01

    Seawater 234U/238U provides global-scale information about continental weathering and is vital for marine uranium-series geochronology. Existing evidence supports an increase in 234U/238U since the last glacial period, but the timing and amplitude of its variability has been poorly constrained. Here we report two seawater 234U/238U records based on well-preserved deep-sea corals from the low-latitude Atlantic and Pacific Oceans. The Atlantic 234U/238U started to increase before major sea-level rise and overshot the modern value by 3 per mil during the early deglaciation. Deglacial 234U/238U in the Pacific converged with that in the Atlantic after the abrupt resumption of Atlantic meridional overturning. We suggest that ocean mixing and early deglacial release of excess 234U from enhanced subglacial melting of the Northern Hemisphere ice sheets have driven the observed 234U/238U evolution.

  3. Energy dependence of 238U fission yields investigated in inverse kinematics

    Directory of Open Access Journals (Sweden)

    Veselsky M.

    2010-03-01

    Full Text Available The production cross sections of neutron-rich fission residues produced in reactions induced by a 238U beam impinging onto Pb and Be targets were investigated at the Fragment Separator (FRS at GSI using the inverse kinematic technique. These data allowed us to discuss the optimum energies in fission for producing the most neutron-rich residues.

  4. (234)U/(238)U signatures associated with uranium ore bodies: part 2 Manyingee.

    Science.gov (United States)

    Lowson, Richard T; McIntyre, Mark G

    2013-04-01

    The Manyingee ore body is a roll-front U ore body located at depth in the Cretaceous sandstone sediments of a Proterozoic palaeo valley. It is located in a confined aquifer. The aquifer is recharged 4 km upstream by the Ashburton River. Groundwater samples were collected at and up to 4.7 km downstream of the ore body. The ground water (234)U/(238)U activity ratios (AR) were elevated to 1.86 in the vicinity of the ore body and then declined to 1.06 over the 4.7 km transect. The elevated (234)U/(238)U ARs are attributed to selective leaching of (234)U sites by oxidising waters, with α recoil as a necessary precursor to produce activated (234)U sites. Direct ejection into another phase following α recoil is considered to be a minor contributor to (234)U -(238)U disequilibrium in this environment. The profile is considered to be typical of the (234)U/(238)U AR profile at and down gradient of the redox front of a U ore body.

  5. Magmatic Processes at Loihi Seamount Inferred From 226Ra-230Th-234U-238U Disequilibria

    Science.gov (United States)

    Pietruszka, A. J.; Hauri, E. H.; Garcia, M. O.

    2001-12-01

    We have conducted a detailed study of the U-series isotope geochemistry of young tholeiitic, transitional and alkalic Loihi basalts to examine the melt generation process during the preshield stage of a Hawaiian volcano. A previous study (Sims et al. 1999; GCA, v. 63) of two dredged lavas from the deep flanks of Loihi found a higher (230Th/238U) activity ratio in an alkalic basalt (1.07) compared to a tholeiitic basalt (1.04). This difference suggests that the tholeiitic basalt may have formed at a higher rate of mantle upwelling than the alkalic basalt. Our samples were collected from surface lava flows at Loihi's summit and along the volcano's south rift zone by submersible. Analyses were preformed using high-precision plasma ionization mass spectrometry. The samples display a relatively large range in the amount of excess 226Ra (0-13%) that extends to much lower values than observed at Kilauea Volcano (11-12%). The low (226Ra/230Th) ratios of Loihi lavas probably result from post-eruptive decay of 226Ra and imply eruption ages of 0-12 kyr. All of the Loihi samples (including the 1996 lava) have small amounts of excess 234U (0.2-0.8%). The most likely source for (234U/238U)>1 at Loihi is seawater, which has (234U/238U)=1.14. Since all of the samples were fresh, hand-picked glasses, these elevated (234U/238U) ratios may have resulted from the assimilation of a seawater-derived component within Loihi's magmatic plumbing system rather than post-eruptive U addition. The range of (230Th/238U) that we measured is 1.01-1.07, which is larger than the previous range known for Loihi. Mass balance calculations using the measured (234U/238U) ratios suggest that 1-6% of the U in the samples that we analyzed is ultimately derived from seawater. Correcting the 230Th-238U disequilibria of the Loihi lavas for this seawater-derived U results in a narrower range in the amount of excess 230Th (6-9%) with no significant differences between tholeiitic, transitional or alkalic basalts

  6. Studying nuclear level densities of {sup 238}U in the nuclear reactions within the macroscopic nuclear models

    Energy Technology Data Exchange (ETDEWEB)

    Razavi, Rohallah; Aghajani, Maghsood; Khooy, Asghar [Imam Hossein Comprehensive Univ., Tehran (Iran, Islamic Republic of). Dept. of Physics; Rahmatinejad, Azam; Taheri, Fariba [Univ. of Zanjan (Iran, Islamic Republic of). Dept. of Physics; Kakavand, Tayeb [Imam Khomeini International Univ., Qazvin (Iran, Islamic Republic of). Dept. of Physics

    2016-05-01

    In this work the nuclear level density parameters of {sup 238}U have been extracted in the back-shifted Fermi gas model (BSFGM), as well as the constant temperature model (CTM), through fitting with the recent experimental data on nuclear level densities measured by the Oslo group. The excitation functions for {sup 238}U(p,2nα){sup 233}Pa, and {sup 238}U(p,4n){sup 235}Np reactions and the fragment yields for the fragments of the {sup 238}U(p,f) reaction have been calculated using obtained level density parameters. The results are compared to their corresponding experimental values. It was found that the extracted excitation functions and the fragment yields in the CTM coincide well with the experimental values in the low-energy region. This finding is according to the claim made by the Oslo group that the extracted level densities of {sup 238}U show a constant temperature behaviour.

  7. 238U, and its decay products, in grasses from an abandoned uranium mine

    Science.gov (United States)

    Childs, Edgar; Maskall, John; Millward, Geoffrey

    2016-04-01

    Bioaccumulation of radioactive contaminants by plants is of concern particularly where the sward is an essential part of the diet of ruminants. The abandoned South Terras uranium mine, south west England, had primary deposits of uraninite (UO2) and pitchblende (U3O8), which contained up to 30% uranium. When the mine was active uranium and radium were extracted but following closure it was abandoned without remediation. Waste rock and gangue, consisting of inefficiently processed minerals, were spread around the site, including a field where ruminants are grazed. Here we report the activity concentrations of 238U, 235U 214,210Pb, and the concentrations of selected metals in the soils, roots and leaves of grasses taken from the contaminated field. Soil samples were collected at the surface, and at 30 cm depth, using an auger along a 10-point transect in the field from the foot of a waste heap. Whole, individual grass plants were removed with a spade, ensuring that their roots were intact. The soils and roots and grass leaves were freeze-dried. Activity concentrations of the radionuclides were determined by gamma spectroscopy, following 30 days incubation for development of secular equilibrium. Dried soils, roots and grasses were also digested in aqua regia and the concentrations of elements determined by ICP techniques. Maximum activity concentrations of 238U, 235U, 214Pb and 210Pb surface soils were 63,300, 4,510, 23,300 and 49,400 Bq kg-1, respectively. The mean 238U:235U ratio was 11.8 ± 1.8, an order of magnitude lower than the natural value of 138, indicating disequilibrium within the decay chain due to mineral processing. Radionuclides in the roots had 5 times lower concentration and only grass leaves in the vicinity of the waste heap had measureable values. The mean soil to root transfer factor for 238U was 36%, the mean root to leaf was 3% and overall only 0.7% of 238U was transferred from the soil to the leaves. The roots contained 0.8% iron, possibly as

  8. Measurement of neutron inelastic scattering cross section of {sup 238}U

    Energy Technology Data Exchange (ETDEWEB)

    Miura, Takako; Baba, Mamoru; Ibaraki, Masanobu; Sanami, Toshiya; Win, Than; Hirasawa, Yoshitaka; Matsuyama, Shigeo; Hirakawa, Naohiro [Tohoku Univ., Sendai (Japan)

    1998-03-01

    Neutron scattering from the 0{sup +}, 2{sup +} (1-st) and 4{sup +} (2nd) levels of {sup 238}U was measured for incident energies between 0.4 and 0.85 MeV at the Tohoku University 4.5 MV Dynamitron facility, using the time-of-flight (TOF) method with monoenergetic pulsed neutrons by the {sup 7}Li(p,n) reaction. The results are presented in comparison with other experimental data and evaluated data. (author)

  9. Determination of 235U/238U Ratio on Urine by ICP-MS

    Energy Technology Data Exchange (ETDEWEB)

    Collins, L; Gobaleza, A; Langston, R; Radev, R; Than, C; Wong, C; Wood-Zika, A

    2011-10-19

    LLNL Internal Dosimetry Program - The new procedure satisfies the requirement to determine {sup 235}U/{sup 238}U ratio in bioassay urine samples. MDA - The L{sub C} and MDA{sub 95} for {sup 235}U are well below the required detection limit of 0.00035 {mu}g/L. Turn around time - Analysis of 10 samples plus 2 QCs can be completed in one work day (8 hours).

  10. Measurement of Prompt Fission Neutron Spectrum of 238U at 2.8 MeV

    Institute of Scientific and Technical Information of China (English)

    HUANG; Han-xiong; RUAN; Xi-chao; REN; Jie; LI; Guang-wu; LUAN; Guang-yuan

    2015-01-01

    The prompt fission neutron spectrum(PFNS,Fig.1)of 238U was measured at 2.8MeV incident neutron energy by using the Cockcroft&Walton accelerator in China Institute of Atomic Energy(CIAE).The effect-to-background ratio was improved by increasing the amount of sample mass and adding an appropriate shielding.The final uncertainty of neutron energy spectrum is less than 20%below 10MeV region at an bin size

  11. An Analysis of 178Pb to 238U Isotopes with the Universal and Yukawa Proximity Potentials

    Science.gov (United States)

    Javadimanesh, E.; Hassanabadi, H.; Zarrinkamar, S.

    2013-07-01

    The alpha particle preformation and the penetration probability by the Yukawa proximity potential in the even-even nuclei from 178Pb to 238U are studied. Using the experimental values of the alpha decay half-lives and the decay energies, we extract the preformation factors and the penetration probabilities. We also calculate the assault frequencies and the decay constants. The obtained results are motivating.

  12. Studies of positron electron pair production in {sup 238}U + {sup 232}Th

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, I.; Back, B.B.; Betts, R.R. [and others

    1995-08-01

    Following the non-observation of sharp sum-energy lines in our earlier {sup 238}U + {sup 181}Ta measurements, it was decided to pursue measurements of the {sup 238}U + {sup 232}Th system which, in the previously published work, showed the most striking evidence for near-equal-energy back-to-back pairs leading to sharp sum-energy lines. Following the refurbishing of the APEX silicon arrays and extensive tests of the rotating target wheel assembly, a major positron run took place in November 1994. Rolled 1-mg/cm{sub 2} {sup 232}Th targets were bombarded with 5.95-MeV/u {sup 238}U. The target rotation allowed up to 2 pnA of beam to be used without serious deterioration of the targets. Over 300,000 pairs were accumulated, representing an order-of-magnitude improvement in statistics over the previously published results. Preliminary analysis shows no evidence for the sharp lines at a cross section level orders of magnitude below those previously reported. The analysis of these data is currently being completed in preparation for publication.

  13. Solubility of 238U radionuclide from various types of soil in synthetic gastrointestinal fluids using "US in vitro" digestion method

    Science.gov (United States)

    Rashid, Nur Shahidah Abdul; Sarmani, Sukiman; Majid, Amran Ab.; Mohamed, Faizal; Siong, Khoo Kok

    2015-04-01

    238U radionuclide is a naturally occuring radioactive material that can be found in soil. In this study, the solubility of 238U radionuclide obtained from various types of soil in synthetic gastrointestinal fluids was analysed by "US P in vitro" digestion method. The synthetic gastrointestinal fluids were added to the samples with well-ordered, mixed throughly and incubated according to the human physiology digestive system. The concentration of 238U radionuclide in the solutions extracted from the soil was measured using Induced Coupling Plasma Mass Spectrometer (ICP-MS). The concentration of 238U radionuclide from the soil samples in synthetic gastrointestinal fluids showed different values due to different homogenity of soil types and chemical reaction of 238U radionuclide. In general, the solubility of 238U radionuclide in gastric fluid was higher (0.050 - 0.209 ppm) than gastrointestinal fluids (0.024 - 0.050 ppm). It could be concluded that the US P in vitro digestion method is practicle for estimating the solubility of 238U radionuclide from soil materials and could be useful for monitoring and risk assessment purposes applying to environmental, health and contaminated soil samples.

  14. The inflow of 234U and 238U from the River Odra drainage basin to the Baltic Sea

    Directory of Open Access Journals (Sweden)

    Bogdan Skwarzec

    2010-12-01

    Full Text Available In this study the activity of uranium isotopes 234U and 238U in Odra river water samples, collected from October 2003 to July2004, was measured using alpha spectrometry. The uranium concentrations were different in each of the seasons analysed; the lowest values were recorded in summer. In all seasons, uranium concentrations were the highest in Bystrzyca river waters (from 27.81 ± 0.29Bq m-3 of 234U and 17.82 ± 0.23 Bq m-3 of 238U in spring to 194.76 ± 3.43 Bq m-3 of 234U and 134.88 ± 2.85 Bq m-3 of 238U in summer. The lowest concentrations were noted in the Mała Panew (from 1.33 ± 0.02 Bq m-3 of 234U and 1.06 ± 0.02 Bq m-3 of 238U in spring to 3.52 ± 0.05 Bq m-3 of 234U and 2.59± 0.04 Bq m-3 of 238U in autumn. The uranium radionuclides 234U and 238U in the water samples were not in radioactive equilibrium. The 234U / 238U activity ratios were the highest in Odra water samples collected at Głogów (1.84 in autumn, and the lowest in water from the Noteć (1.03 in winter and spring. The 234U / 238U activity ratio decreases along the main stream of the Odra, owing to changes in the salinity of the river's waters. Annually, 8.19 tons of uranium (126.29 G Bq of 234U and 100.80 G Bq of 238U flow into the Szczecin Lagoon with Odra river waters.

  15. Monte Carlo and deterministic simulations of activation ratio experiments for 238U(n,f), 238U(n,g) and 238U(n,2n) in the Big Ten benchmark critical assembly

    Energy Technology Data Exchange (ETDEWEB)

    Descalle, M; Clouse, C; Pruet, J

    2009-07-28

    The authors have compared calculations of critical assembly activation ratios using 3 different Monte Carlo codes and one deterministic code. There is excellent agreement. Discrepancies between the different Monte Carlo codes are the 1-2% level. Notably, the deterministic calculations with 87 groups are also in good agreement with the continuous energy Monte Carlo results. The three codes underestimate the {sup 238}U(n,f) reaction, suggesting that there is room for improvement in the evaluation, or in the evaluations of other reactions influencing the spectrum in BigTen. Until statistical uncertainties are implemented in Mercury, they strongly advise long runs to guarantee sufficient convergence of the flux at high energies, and they strongly encourage comparing Mercury results to a well-developed and documented code such as MCNP5 and/or COG. It may be that ENDL2008 will be available for use in COG within a year. Finally, it may be worthwhile to add a 'standard' reaction rate tally similar to those implemented in COG and MCNP5, if the goal is to expand the central fission and activation ratios simulations to include isotopes that are not part of the specifications for the assembly material composition.

  16. Determination of sup 238 U in marine organisms by inductively coupled plasma mass spectrometry. Yudo ketsugo plasma shitsuryo bunsekiho ni yoru kaiyo seibutsuchu no sup 238 U no teiryo

    Energy Technology Data Exchange (ETDEWEB)

    Ishii, T.; Nakahara, M; Matsuda, M.; Ishikawa, M. (National Institute of Radiological Sciences, Ibaraki (Japan))

    1991-05-25

    Since the {sup 238} U concentration in seawater is about 3ng/ml at the element level and the activity concentration is 40 {mu} Bq/ml which are considerably higher that those of other {alpha} radioactive materials, it is necessary to study the concentration levels of many marine organisms. After confirming that the inductively coupled plasma mass spectrometry as a new high sensitive analysis for multi-elements is effective to analyze heavy elements such as rare earth elements or uranium, etc., this method was applied to determine {sup 238} U in 55 species of marine organism. The {sup 238} U concentration in soft tissues of marine animal ranged from 0.076 to 5000ng/g wet weight and large difference of concentration was observed depending on the kind of animal and the tissue. Especially, the branchial heart of cephalopod molluscs showed the specific accumulation of {sup 238} U. The concentration factor of branchial heart of Octopus vulgaris which showed the highest value was calculated to be about 10 {sup 3} by comparing it with the concentration of {sup 238} U in Japanese coastal waterseas. The concentration of {sup 238} U in 20 species of algae ranged from 10 to 3700ng/g dry weight. 11 refs., 2 figs., 9 tabs.

  17. Generation of 238U Covariance Matrices by Using the Integral Data Assimilation Technique of the CONRAD Code

    Directory of Open Access Journals (Sweden)

    Privas E.

    2016-01-01

    Full Text Available A new IAEA Coordinated Research Project (CRP aims to test, validate and improve the IRDF library. Among the isotopes of interest, the modelisation of the 238U capture and fission cross sections represents a challenging task. A new description of the 238U neutrons induced reactions in the fast energy range is within progress in the frame of an IAEA evaluation consortium. The Nuclear Data group of Cadarache participates in this effort utilizing the 238U spectral indices measurements and Post Irradiated Experiments (PIE carried out in the fast reactors MASURCA (CEA Cadarache and PHENIX (CEA Marcoule. Such a collection of experimental results provides reliable integral information on the (n,γ and (n,f cross sections. This paper presents the Integral Data Assimilation (IDA technique of the CONRAD code used to propagate the uncertainties of the integral data on the 238U cross sections of interest for dosimetry applications.

  18. Background reduction in {sup 236}U/{sup 238}U measurements

    Energy Technology Data Exchange (ETDEWEB)

    Buompane, Raffaele [CIRCE, Dipartimento di Matematica e Fisica, Seconda Università degli Studi di Napoli and INNOVA, Caserta (Italy); INFN sezione di Napoli (Italy); De Cesare, Mario [Department of Nuclear Physics, The Australian National University, ACT 2601 (Australia); De Cesare, Nicola [CIRCE, Dipartimento di Matematica e Fisica, Seconda Università degli Studi di Napoli and INNOVA, Caserta (Italy); INFN sezione di Napoli (Italy); Di Leva, Antonino [INFN sezione di Napoli (Italy); Dipartimento di Fisica, Università di Napoli “Federico II” (Italy); D’Onofrio, Antonio [CIRCE, Dipartimento di Matematica e Fisica, Seconda Università degli Studi di Napoli and INNOVA, Caserta (Italy); INFN sezione di Napoli (Italy); Fifield, L. Keith; Fröhlich, Michaela [Department of Nuclear Physics, The Australian National University, ACT 2601 (Australia); Gialanella, Lucio; Marzaioli, Fabio; Sabbarese, Carlo; Terrasi, Filippo [CIRCE, Dipartimento di Matematica e Fisica, Seconda Università degli Studi di Napoli and INNOVA, Caserta (Italy); INFN sezione di Napoli (Italy); Tims, Stephen; Wallner, Anton [Department of Nuclear Physics, The Australian National University, ACT 2601 (Australia)

    2015-10-15

    The measurements of actinide isotopic ratios, in particular {sup 236}U/{sup 238}U, in environmental samples requires high sensitivity. In particular, special effort must be devoted to the suppression of interfering nuclides, such as {sup 235,238}U, when measuring {sup 236}U. At the AMS facility of CIRCE, isotopic ratios down to ∼10{sup −10} are currently measured using a gas E − ΔE detector. In order to push this limit lower towards natural levels, a time-of-flight system is used, featuring a micro-channel plate start detector and a Si stop detector. As the mass resolution of the latter is limited by the layout, an attempt to reduce the abundant isotope interference by other means has been undertaken. In this study, we report preliminary results on the characterization of the presence of molecular interferences when using UO{sup −}, UC{sup −} and UC{sub 2}{sup −} as injected molecular ions. In particular the possibility to stabilize the current yield from carbide cathodes has been investigated: it was found that the best cathode preparation procedure is obtained pressing U salts baked at 800 °C mixed with graphite and Al powder. Moreover, the {sup 238}U background in {sup 236}U measurements is strongly reduced injecting UC{sup −} ions, as verified using a time-of-flight detection system. On the other hand, {sup 235}U interference is larger with respect to UO{sup −} injection, but this increase is smaller than expected on the basis of abundances of {sup 13}C and {sup 17}O in UC and UC{sub 2} molecules on one side and UO, on the other.

  19. Potential Energy Surfaces of the Even-Even 230-238 U Isotopes

    Directory of Open Access Journals (Sweden)

    Diab S. M.

    2008-07-01

    Full Text Available Nuclear structure of 230 - 238 U isotopes have been studied in the frame work of the in- teracting boson approximation model (IBM-I. The contour plot of the potential energy surfaces, V ( ; , shows that all nuclei are deformed and have rotational char- acters, SU (3 . Levels energy spectra belonging to the gsb , , bands, electromagnetic transition rates B ( E 1 and B ( E 2 , quadrupole moment Q 0 , deformation parameterare 2 and the strength of the electric monopole transitions X ( E 0 =E 2 are calculated. The calculated values are compared with the available theoretical and experimental data and show reasonable agreement.

  20. Intermediate structure in the /sup 238/U neutron capture cross section

    Energy Technology Data Exchange (ETDEWEB)

    Perez, R.B.; de Saussure, G.

    1975-10-01

    Recent measurements of the /sup 238/U neutron capture cross section show large fluctuations in the unresolved resonance region. To test whether or not the observed long-range fluctuation of the neutron capture represent departures from the compound nuclear model, the Wald-Wolfowitz runs and correlation tests were applied to the /sup 238/U neutron capture data obtained at ORELA. The Wald-Wolfowitz runs test deals with the statistic, R, which is the number of unbroken sequences of data points above or below a given reference line. This statistic is to be compared with the expected value of runs E(R) +- sigma(R) arising from randomly distributed data. In the correlation test we have computed the first serial correlation coefficient of the data as well as its expected value and variance for a set of random data. In both tests one computes the probability, P, for the given statistical entity to depart from its expected value by more than epsilon standard deviations. Both tests confirm the presence of intermediate structure between 5 and 100 keV. The range of the structure far exceeds the width of the experimental resolution and level widths. 3 tables, 2 figures. (auth)

  1. The dependence of cumulative 238U(n,f) fission yield on incident-neutron energy

    Institute of Scientific and Technical Information of China (English)

    ZHENG Na; ZHONG Chunlai; MA Liyong; CHEN Zhongjing; LI Xiangqing; LIU Tingjin; CHEN Jinxiang; FAN Tieshuan

    2009-01-01

    This work is aim at studying the dependence of fission yields on incident neutron energy,so as to produce evaluated yield sets of the energy dependence.Experimental data at different neutron energies for gas fission products 85m,87,88Kr and 138Xe resulting from the 238U(n,f) reaction are processed using codes AVERAGE for weighed average and ZOTT for simultaneous evaluation.Energy dependence of the cumulative fission product yields on the incident neutron is presented.The evaluated curve of product yield is compared with the results calculated by the TALYS-0.64 code.The present evaluation is consistent with other main libraries in error permission.The fit curve of 87,88Kr can be recommended to predict the unmeasured fission yields.Comparisons of the evaluated energy dependence curves with theoretical calculated results show that the predictions using purely theoretical model for the fission process are not sufficiently accurate and reliable for the calculations of the cumulative fission yields for the 238U(n,f).

  2. The low-energy dipole structure of 232Th , 236U and 238U actinide nuclei

    Science.gov (United States)

    Kuliev, A. A.; Guliyev, E.; Ertugral, F.; Özkan, S.

    2010-03-01

    In this study, ensuremath I^{π} = 1+ and ensuremath I^{π} = 1- dipole mode excitations are systematically investigated within the rotational and translational + Galilean invariant quasiparticle random-phase approximation for 232Th , 236U , and 238U actinide nuclei. It is shown that the investigated nuclei reach a B( M1) strength structure, which corresponds to the scissors mode. The calculated mean excitation energies as well as the summed B( M1) value of the scissors mode excitations are consistent with the available experimental data. The results of calculations indicate large differences to the rare-earth nuclei as is the case for the experiment: a doubling of the observed dipole strengths and a shift of the energy centroid to the lower energies by about 800keV. The calculations indicate the presence of a few prominent negative-parity ensuremath K^{π} = 1- states in the 2.0-4.0MeV energy interval. The occurrence of the negative-parity dipole states with the rather high B( E1) value less than 4MeV shows the necessity of explicit parity measurements for the correct determination of the scissors mode strength in 232Th , 236U , and 238U isotopes.

  3. (238)U and total radioactivity in drinking waters in Van province, Turkey.

    Science.gov (United States)

    Selçuk Zorer, Özlem; Dağ, Beşir

    2014-06-01

    As part of the national survey to evaluate natural radioactivity in the environment, concentration levels of total radioactivity and natural uranium have been analysed in drinking water samples. A survey to study natural radioactivity in drinking waters was carried out in the Van province, East Turkey. Twenty-three samples of drinking water were collected in the Van province and analysed for total α, total β and (238)U activity. The total α and total β activities were counted by using the α/β counter of the multi-detector low background system (PIC MPC-9604), and the (238)U concentrations were determined by inductively coupled plasma-mass spectrometry (Thermo Scientific Element 2). The samples were categorised according to origin: tap, spring or mineral supply. The activity concentrations for total α were found to range from 0.002 to 0.030 Bq L(-1) and for total β from 0.023 to 1.351 Bq L(-1). Uranium concentrations ranging from 0.562 to 14.710 μg L(-1) were observed in drinking waters. Following the World Health Organisation rules, all investigated waters can be used as drinking water.

  4. Natural Activities of 238U, 232Th and 40K in Manganese Ore

    Directory of Open Access Journals (Sweden)

    H. A. Abel-Ghany

    2010-01-01

    Full Text Available Problem statement: Manganese ore is widely used in much industries. Such as ore contain natural radioactive nuclides at various concentrations. If this ore contain high concentrations of natural radioactive nuclides, workers handling them might be exposed to significant levels of radiation. Therefore it is important to determine the radioactive nuclides in this ore. Approach: The natural radionuclides (238U, 232Th and 40K contents of Manganese ore samples collected by Siani Manganese Company in Egypt-Cairo have been determined by low background spectroscopy using hyper-pure germanium (HPGe detector. Results: The mean activities due to the three radionuclides (238U, 232Th and40K were found to be 3543±106, 222±6.6 and 3483±104 Bqkg-1, respectively. The absorbed dose rate due to the natural radioactivity in samples under investigation ranged from 1522±45-1796±53 nGyh-1. The radium equivalent activity varied from 3807±114-4446±133 Bqkg-1. The representative external hazard index values for the corresponding samples are also estimated. Conclusion: The results of this assessment obtained by the gamma-ray spectroscopic analysis, have indicated that the levels of natural radioactivity were higher than the international recommended limits.

  5. Analysis of the {sup 238}U resonance parameters using random-matrix theory

    Energy Technology Data Exchange (ETDEWEB)

    Courcelle, A. [CEA Cadarache, 13 - Saint Paul lez Durance (France); Derrien, H.; Leal, L.C.; Larson, N.M. [Oak Ridge National Laboratory, Oak Ridge, TN (United States)

    2005-07-01

    Random-matrix theories (RMTs) provide valuable statistical tools to analyze neutron-resonance data. The predictive power of the random-matrix theories, which do not contain any adjustable parameters, is striking, and the application is rather simple and fast. A new evaluation of {sup 238}U resonance parameters has recently been performed at the Oak Ridge National Laboratory; the objective of this paper is to illustrate the use of RMT in the field of resonance-parameter evaluation with the newly evaluated {sup 239}U energy levels and widths. Several statistics were computed using the s-wave resonances up to 20 keV and compared to the Gaussian Orthogonal Ensemble predictions. It is shown that a good agreement is observed between RMT and the experimental data up to 2.5 keV. The F-Dyson statistic was especially investigated because of its claimed ability to detect locally missed and spurious levels in the sample (p-resonances contamination or unresolved multiplets). As expected, the entire set of evaluated {sup 238}U s-wave resonances up to 20 keV disagrees significantly with the theory. There are two reasons for this: First, it is difficult to distinguish s- and p-wave resonances in the analysis. Secondly, especially above 10 keV, it is impossible to determine reliable resonance energies from the available experimental data. It is concluded that the use of RMT can help nuclear data specialists to improve their evaluations in the resonance range. (authors)

  6. Photofission product yields of 238U and 239Pu with 22-MeV bremsstrahlung

    Science.gov (United States)

    Wen, Xianfei; Yang, Haori

    2016-06-01

    In homeland security and nuclear safeguards applications, non-destructive techniques to identify and quantify special nuclear materials are in great demand. Although nuclear materials naturally emit characteristic radiation (e.g. neutrons, γ-rays), their intensity and energy are normally low. Furthermore, such radiation could be intentionally shielded with ease or buried in high-level background. Active interrogation techniques based on photofission have been identified as effective assay approaches to address this issue. In designing such assay systems, nuclear data, like photofission product yields, plays a crucial role. Although fission yields for neutron-induced reactions have been well studied and readily available in various nuclear databases, data on photofission product yields is rather scarce. This poses a great challenge to the application of photofission techniques. In this work, short-lived high-energy delayed γ-rays from photofission of 238U were measured in between linac pulses. In addition, a list-mode system was developed to measure relatively long-lived delayed γ-rays from photofission of 238U and 239Pu after the irradiation. Time and energy information of each γ-ray event were simultaneously recorded by this system. Cumulative photofission product yields were then determined using the measured delayed γ-ray spectra.

  7. Symmetric splitting for the system 32S+238U at energies near and below the barrier

    Science.gov (United States)

    Freifelder, R.; Braun-Munzinger, P.; Deyoung, P.; Schicker, R.; Sen, S.; Stachel, J.

    1987-06-01

    The total capture cross section for the system 32S+238U has been measured at energies from 0.93 to 1.08 times the s-wave interaction barrier by detecting coincident fission fragments following full momentum transfer reactions. The subbarrier cross section cannot be reproduced by a one-dimensional barrier penetration model. Using a quantum mechanical coupled channels model, good agreement is obtained. The measured angular distributions of fission fragments were compared to the predictions of saddle and scission point transition state theory. Saddle point transition state model calculations fail to reproduce the data, while scission point transition state calculations are in agreement with their qualitative trend. Evidence for nonequilibrium processes is presented.

  8. Studies of positron electron pair production in {sup 238}U + {sup 181}Ta

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, I.; Back, B.B.; Betts, R.R. [and others

    1995-08-01

    Following the completion of APEX in late 1993, a two-week run on the {sup 238}U + {sup 181}Ta system at 6.1 and 6.3 MeV/u with 1 mg/cm{sup 2} targets provided, for the first time, data in which the expected sharp sum-energy lines should appear. Data from previous experiments show evidence for sharp sum-energy lines at 625, 748 and 805 keV, observed at bombarding energies from 5.9 to 6.3 MeV/u. The 625- and 809-keV lines display the characteristics of equal-energy back-to-back emission whereas the 748-keV line shows a rather different behavior. In our measurements, average beam currents of 2-3 pnA from the ATLAS accelerator were used to bombard 1-mg/cm{sup 2} rolled {sup 181}Ta targets, the energy loss in which corresponds to the ranges of bombarding energies over which the sharp sum-energy lines were previously reported. A run at 5.95 MeV/u for {sup 238}U + {sup 181}Ta followed in May 1994. These data were analyzed extensively. Sum-energy spectra measured in coincidence with scattered ions in the range 20{degrees} < {theta} < 68{degrees}. No evidence is found for the sharp sum-energy lines reported previously and, depending on the scenario assumed for the production mechanism and kinematics of the pairs, upper limits on cross sections at the 90% confidence limit range from 10-100 times smaller than the values that can be deduced from the earlier reports. We are in the process of refining the data analysis and simulations of the apparatus in order to finalize these numbers for publication.

  9. 238 U, 232 Th and 40 K in wheat flour samples of Iraq markets

    Directory of Open Access Journals (Sweden)

    A. A.

    2014-09-01

    Full Text Available Introduction. Wheat flour is a nutritious type of food that is widely consumed by various age groups in Iraq. This study investigates the presence of long-lived gamma emitters in different type of wheat flour in Iraqi market. Materials and methods. Uranium ( 238 U, Thorium ( 232 Th and Potassium ( 40 K specific activity in (Bq/kg were measured in (12 different types of wheat flours that are available in Iraqi markets. The gamma spectrometry method with a NaI(Tl detector has been used for radiometric measurements. Also in this study we have calculated the internal hazard index, radium equivalent and absorbed dose rate in all samples. Results and discussion. It is found that the specific activity in wheat flour samples were varied from (1.086±0.0866 Bq/kg to (12.532±2.026 Bq/kg with an average (6.6025 Bq/kg for 238 U, For 232 Th From (0.126±0.066 Bq/kg to (4.298±0.388 Bq/kg with an average (1.9465Bq/kg and for 40 K from (41.842±5.875 Bq/kg to (264.729±3.843 Bq/kg with an average (133.097 Bq/kg. Also, it is found that the radium equivalent and the internal hazard index in wheat flour samples ranged from (3.4031 Bq/kg to (35.1523 Bq/kg with an average (19.6346 Bq/kg and from (0.0091 to (0.1219 with an average (0.0708 respectively. Conclusion. This study prove that the natural radioactivity and radiation hazard indices were lower than the safe.

  10. 238 U, 232 Th and 40 K in wheat flour samples of Iraq markets

    Directory of Open Access Journals (Sweden)

    Ali Abid Abojassim

    2015-05-01

    Full Text Available Introduction. Wheat flour is a nutritious type of food that is widely consumed by various age groups in Iraq. This study investigates the presence of long-lived gamma emitters in different type of wheat flour in Iraqi market. Materials and methods. Uranium (238 U, Thorium (232 Th and Potassium (40 K specific activity in (Bq/kg were measured in (12 different types of wheat flours that are available in Iraqi markets. The gamma spectrometry method with a NaI(Tl detector has been used for radiometric measurements. Also in this study we have calculated the internal hazard index, radium equivalent and absorbed dose rate in all samples. Results and discussion. It is found that the specific activity in wheat flour samples were varied from (1.086±0.0866 Bq/kg to (12.532±2.026 Bq/kg with an average (6.6025 Bq/kg for 238 U, For 232 Th From (0.126±0.066 Bq/kg to (4.298±0.388 Bq/kg with an average (1.9465Bq/kg and for 40 K from (41.842±5.875 Bq/kg to (264.729±3.843 Bq/kg with an average (133.097 Bq/kg. Also, it is found that the radium equivalent and the internal hazard index in wheat flour samples ranged from (3.4031 Bq/kg to (35.1523 Bq/kg with an average (19.6346 Bq/kg and from (0.0091 to (0.1219 with an average (0.0708 respectively. Conclusion. This study prove that the natural radioactivity and radiation hazard indices were lower than the safe.

  11. Fluxes of 238U decay series radionuclides in a dicalcium phosphate industrial plant.

    Science.gov (United States)

    Casacuberta, N; Masqué, P; Garcia-Orellana, J

    2011-06-15

    The production of dicalcium phosphate (DCP) is part of the phosphate industry, which has been recently included in the positive list of the NORM industries defined in the revised version of the EU-BSS (Euratom 29/96). The objective of the present work is to study specific concentrations and fluxes of (238,234)U, (230)Th, (226)Ra, (210)Pb and (210)Po at the different stages of the DCP production. Results showed highest activities of (238)U and (210)Pb were found in DCP (1500-2000 Bq kg(-1)); (230)Th and (210)Po were released together with the sludges (1600-2000 Bq kg(-1)) and (226)Ra presented particularly high activities in water (48 × 10(3) Bq m(-3)) and in the reactor scales (115 × 10(3) Bq kg(-1)). Fluxes of radionuclides showed that (238)U outflows were equally distributed between sludges (16 × 10(3) kBq h(-1)) and dicalcium phosphate (20 × 10(3) kBq h(-1)); (230)Th and (210)Po were almost entirely released in the sludges (30 × 10(3)kBq h(-1)) and the greatest (210)Pb outflow was the DCP current (25 × 10(3) kBq h(-1)). (226)Ra was mainly discharged through the water effluent (12 × 10(3) kBq h(-1)). This work highlights the importance of studying the industrial processes involving NORM, as minor changes in the production steps lead to different radionuclide distribution in the process.

  12. Fluxes of {sup 238}U decay series radionuclides in a dicalcium phosphate industrial plant

    Energy Technology Data Exchange (ETDEWEB)

    Casacuberta, N., E-mail: Nuria.Casacuberta@uab.es [Institut de Ciencia i Tecnologia Ambientals - Departament de Fisica, Universitat Autonoma de Barcelona, 08193 Bellaterra (Spain); Masque, P.; Garcia-Orellana, J. [Institut de Ciencia i Tecnologia Ambientals - Departament de Fisica, Universitat Autonoma de Barcelona, 08193 Bellaterra (Spain)

    2011-06-15

    The production of dicalcium phosphate (DCP) is part of the phosphate industry, which has been recently included in the positive list of the NORM industries defined in the revised version of the EU-BSS (Euratom 29/96). The objective of the present work is to study specific concentrations and fluxes of {sup 238,234}U, {sup 230}Th, {sup 226}Ra, {sup 210}Pb and {sup 210}Po at the different stages of the DCP production. Results showed highest activities of {sup 238}U and {sup 210}Pb were found in DCP (1500-2000 Bq kg{sup -1}); {sup 230}Th and {sup 210}Po were released together with the sludges (1600-2000 Bq kg{sup -1}) and {sup 226}Ra presented particularly high activities in water (48 x 10{sup 3} Bq m{sup -3}) and in the reactor scales (115 x 10{sup 3} Bq kg{sup -1}). Fluxes of radionuclides showed that {sup 238}U outflows were equally distributed between sludges (16 x 10{sup 3} kBq h{sup -1}) and dicalcium phosphate (20 x 10{sup 3} kBq h{sup -1}); {sup 230}Th and {sup 210}Po were almost entirely released in the sludges (30 x 10{sup 3} kBq h{sup -1}) and the greatest {sup 210}Pb outflow was the DCP current (25 x 10{sup 3} kBq h{sup -1}). {sup 226}Ra was mainly discharged through the water effluent (12 x 10{sup 3} kBq h{sup -1}). This work highlights the importance of studying the industrial processes involving NORM, as minor changes in the production steps lead to different radionuclide distribution in the process.

  13. Influence of soil structure on the "Fv approach" applied to (238)U and (226)Ra.

    Science.gov (United States)

    Blanco Rodríguez, P; Vera Tomé, F; Lozano, J C

    2017-02-01

    The soil-to-plant transfer factors were determined in a granitic area for the two long-lived uranium series radionuclides (238)U and (226)Ra. With the aim to identify a physical fraction of soil whose concentration correlates linearly with the plant concentration, the soil compartment was analyzed in various stages. An initial study identified the soil compartments as being either bulk soil or its labile fraction. The bulk soil was subsequently divided into three granulometric fractions consisting of: coarse sand, fine sand, and silt and clay. The soil-to-plant transfer of radionuclides for each of these three texture fractions was analyzed. Lastly, the labile fraction was extracted from each textural part, and the activity concentration of the radionuclides (238)U and (226)Ra was measured. In order to assess the influence of soil texture on the soil-to-plant transfer process, we sought to identify possible correlations between the activity concentration in the plant compartment and those found in the different fractions within each soil compartment. The results showed that the soil-to-plant transfer process for uranium and radium depends on soil grain size, where the results for uranium showed a linear relationship between the activity concentration of uranium in the plant and the fine soil fraction. In contrast, a linear relation between the activity concentration of radium in the plant and the soil coarse-sand fraction was observed. Additionally, the presence of phosphate and calcium in the soil of all of the compartments studied affected the soil-to-plant transfer of uranium and radium, respectively.

  14. 238U and 235U isotope fractionation upon oxidation of uranium-bearing rocks by fracture waters

    Science.gov (United States)

    Chernyshev, I. V.; Golubev, V. N.; Chugaev, A. V.; Mandzhieva, G. V.

    2016-10-01

    The variations in 238U/235U values accompanying mobilization of U by fracture waters from uranium-bearing rocks, in which U occurs as a fine impregnation of oxides and silicates, were studied by the high-precision (±0.07‰) MC-ICP-MS method. Transition of U into the aqueous phase in the oxidized state U(VI) is accompanied by its isotope fractionation with enrichment of dissolved U(VI) in the heavy isotope 238U up to 0.32‰ in relation to the composition of the solid phases. According to the sign, this effect is consistent with the tendency of the behavior of 238U and 235U upon interaction of river waters with rocks of the catchment areas [11] and with the effect observed during oxidation of uraninite by the oxygen-bearing NaHCO3 solution [12].

  15. Neutron Capture Cross Sections and Gamma Emission Spectra from Neutron Capture on 234,236,238U Measured with DANCE

    Science.gov (United States)

    Ullmann, J. L.; Mosby, S.; Bredeweg, T. A.; Couture, A. J.; Haight, R. C.; Jandel, M.; Kawano, T.; O'Donnell, J. M.; Rundberg, R. S.; Vieira, D. J.; Wilhelmy, J. B.; Wu, C.-Y.; Becker, J. A.; Chyzh, A.; Baramsai, B.; Mitchell, G. E.; Krticka, M.

    2014-05-01

    A new measurement of the 238U(n, γ) cross section using a thin 48 mg/cm2 target was made using the DANCE detector at LANSCE over the energy range from 10 eV to 500 keV. The results confirm earlier measurements. Measurements of the gamma-ray emission spectra were also made for 238U(n, γ) as well as 234,236U(n, γ). These measurements help to constrain the radiative strength function used in the cross-section calculations.

  16. 238U/235U determinations of some commonly used reference materials and U-bearing accessory minerals (Invited)

    Science.gov (United States)

    Condon, D.; Noble, S.; McLean, N.; Bowring, S. A.

    2009-12-01

    We have determined 238U/235U ratios for a suite of commonly used natural (CRM 112a, SRM 950a, HU-1) and synthetic (IRMM 184 and CRM U500) uranium reference materials in addition to several U-bearing accessory phases (zircon and monazite) by thermal ionisation mass-spectrometry (TIMS) using the IRMM 3636 233U-236U double spike to accurately correct for mass fractionation. The 238U/235U values for the natural uranium reference materials differ, by up to 0.1%, from the widely used ‘consensus’ value (137.88) with all having 238U/235U values less than 137.88. Similarly, initial 238U/235U data from zircon and monazite yield 238U/235U values that are lower than the ‘consensus’ value. The data obtained from U-bearing minerals is used to assess how the uncertainty in the 238U/235U ratio contributes to the systematic discordance observed in 238U/206Pb and 235U/207Pb dates (Mattinson, 2000; Schoene et al., 2006) which has traditionally been wholly attributed to error in the U decay constants. The 238U/235U determinations made on the synthetic reference materials yield results that are considerably more precise and accurate than the certified values (0.02% vs. 0.1% for CRM U500). The calibration of isotopic tracers used for U-daughter geochronology that are partially based upon these reference materials, and the resultant age determinations, will benefit from increased accuracy and precision. Mattinson, J.M., 2000. Revising the “gold standard”—the uranium decay constants of Jaffey et al., 1971. Eos Trans. AGU, Spring Meet. Suppl., Abstract V61A-02. Schoene B., Crowley J.L., Condon D.C., Schmitz M.D., Bowring S.A., 2006, Reassessing the uranium decay constants for geochronology using ID-TIMS U-Pb data. Geochimica et Cosmochimica Acta 70: 426-445

  17. Combined 238U/235U and Pb Isotopics of Planetary Core Material: The Absolute Age of the IVA Iron Muonionalusta

    Science.gov (United States)

    Brennecka, G. A.; Amelin, Y.; Kleine, T.

    2016-08-01

    We report a measured 238U/235U for the IVA iron Muonionalusta. This measured value requires an age correction of ~7 Myr to the previously published Pb-Pb age. This has major implications for our understanding of planetary core formation and cooling.

  18. Vertical flux of particulate organic carbon in the central South China Sea estimated from 234Th-238U disequilibria

    Institute of Scientific and Technical Information of China (English)

    MA Hao; ZENG Zhi; HE Jianhua; CHEN Liqi; YIN Mingduan; ZENG Shi; ZENG Wenyi

    2008-01-01

    234Th-238u disequilibria were applied to examine the particle dynamics in the euphotic zone of the central South China Sea during the spring 2002 cruise. The particulate organic carbon (POC), 234Th (including both dissolved and particulate) and 238U in the water column at three stations were determined. The profiles of 234Th/238U activity ratio at the three stations all showed consistent 234Th deficit as compared to 238U in the upper 100 m water column. Based on the profiles of the dissolved and particulate 234Th and a steady state box model, the dissolved 234Th scavenging rates, the particulate 234Th removal rates and their resident times were quantified. It was found that the POC downward export fluxes out of the upper 100 m euphotic zone ranged from 9.40 to 14.78 mmol.m-2.d-1. The results from this study provide new information for our understanding of carbon biogeochemical cycle in the South China Sea.

  19. Uranium stable isotope fractionation in the Black Sea: Modern calibration of the 238U/235U paleo-redox proxy

    Science.gov (United States)

    Rolison, John M.; Stirling, Claudine H.; Middag, Rob; Rijkenberg, Micha J. A.

    2017-04-01

    The isotopic compositions of redox-sensitive metals, including uranium (U), in marine sediments have recently emerged as powerful diagnostic tracers of the redox state of the ancient ocean-atmosphere system. Reliable interpretation of sedimentary isotopic information requires a thorough understanding of the environmental controls on isotopic fractionation in modern anoxic environments before being applied to the paleo-record. In this study, the relationship between ocean anoxia and the isotopic fractionation of U was investigated in the water column and sediments of the Black Sea, the world's largest anoxic basin. Paired measurements of 238U/235U and U concentration, supported by other redox parameters, were obtained for water column and sediment samples collected during the 2013 GA04N GEOTRACES expedition to the Black Sea. Removal of U from the water column occurs during the redox transition of soluble U(VI) to relatively insoluble U(IV), resulting in up to 43% of U being removed from solution in euxinic bottom waters. Uranium reduction and removal is accompanied by a progressive shift in 238U/235U towards isotopically light values in the water column as heavier 238U is preferentially exported to sediments over lighter 235U. This gives rise to apparent isotope enrichment factors of ε = -0.63 ± 0.09‰ and ε = -0.84 ± 0.11‰ when U removal is modelled by Rayleigh and closed system equilibrium isotope fractionation, respectively. These ε values fall within the range determined for bacterial U reduction experiments, and together with a striking correlation between the distributions of U and H2S, implicate microbially-mediated U(VI)-U(IV) reduction as the primary mechanism controlling U isotopic shifts in the Black Sea. The 238U/235U of underlying sediments is related to the the 238U/235U of Black Sea bottom waters through the isotope enrichment factor of the U reduction reaction but the relationship between sedimentary and water column 238U/235U is complicated

  20. Mass yield distributions of fission products from photo-fission of {sup 238}U induced by 11.5-17.3 MeV bremsstrahlung

    Energy Technology Data Exchange (ETDEWEB)

    Naik, H.; Goswami, A. [Bhabha Atomic Research Centre, Radiochemistry Division, Mumbai (India); Carrel, Frederick; Laine, Frederic; Sari, Adrien [SAPHIR Facility, Gif-sur-Yvette (France); Kim, G.N. [Kyungpook National University, Department of Physics, Daegu (Korea, Republic of); Normand, S. [Laboratory of Sensors and Elctronics Architectures CEA, Gif-sur-Yvette (France)

    2013-07-15

    The yields of various fission products in the 11.5, 13.4, 15.0 and 17.3 MeV bremsstrahlung-induced fission of {sup 238}U have been determined by recoil catcher and an off-line {gamma}-ray spectrometric technique using the electron linac, SAPHIR at CEA, Saclay, France. The mass yield distributions were obtained from the fission product yields using charge-distribution corrections. The peak-to-valley (P/V) ratio, average light mass (left angle A{sub L} right angle) and heavy mass (left angle A{sub H} right angle) and average number of neutrons (left angle v right angle) in the bremsstrahlung-induced fission of {sup 238}U at different excitation energies were obtained from the mass yield data. From the present and literature data in the {sup 238}U ({gamma}, f) and {sup 238}U (n, f) reactions at various energies, the following observations were obtained: i) The mass yield distributions in the {sup 238}U ({gamma}, f) reaction at various energies of the present work are double-humped, similar to those of the {sup 238}U (n, f) reaction of comparable excitation energy. ii) The yields of fission products for A = 133-134, A = 138-140, and A = 143-144 and their complementary products in the {sup 238}U ({gamma}, f) reaction are higher than other fission products due to the nuclear structure effect. iii) The yields of fission products for A = 133-134 and their complementary products are slightly higher in the {sup 238}U ({gamma}, f) than in the {sup 238}U (n, f), whereas for A = 138-140 and 143-144 and their complementary products are comparable. iv) With excitation energy, the increase of yields of symmetric products and the decrease of the peak-to-valley (P/V ratio in the {sup 238}U ({gamma}, f) reaction is similar to the {sup 238}U (n, f) reaction. v) The increase of left angle v right angle with excitation energy is also similar between the {sup 238}U ({gamma}, f) and {sup 238}U (n, f) reactions. However, it is surprising to see that the left angle A{sub L} right angle and

  1. Mass yield distributions of fission products from photo-fission of 238U induced by 11.5-17.3 MeV bremsstrahlung

    Science.gov (United States)

    Naik, H.; Carrel, Frédérick; Kim, G. N.; Laine, Frédéric; Sari, Adrien; Normand, S.; Goswami, A.

    2013-07-01

    The yields of various fission products in the 11.5, 13.4, 15.0 and 17.3 MeV bremsstrahlung-induced fission of 238U have been determined by recoil catcher and an off-line γ-ray spectrometric technique using the electron linac, SAPHIR at CEA, Saclay, France. The mass yield distributions were obtained from the fission product yields using charge-distribution corrections. The peak-to-valley ( P/ V ratio, average light mass () and heavy mass () and average number of neutrons () in the bremsstrahlung-induced fission of 238U at different excitation energies were obtained from the mass yield data. From the present and literature data in the 238U ( γ, f ) and 238U ( n, f ) reactions at various energies, the following observations were obtained: i) The mass yield distributions in the 238U ( γ, f ) reaction at various energies of the present work are double-humped, similar to those of the 238U ( n, f ) reaction of comparable excitation energy. ii) The yields of fission products for A = 133-134, A = 138-140, and A = 143-144 and their complementary products in the 238U ( γ, f) reaction are higher than other fission products due to the nuclear structure effect. iii) The yields of fission products for A = 133-134 and their complementary products are slightly higher in the 238U ( γ, f ) than in the 238U ( n, f ) , whereas for A = 138-140 and 143-144 and their complementary products are comparable. iv) With excitation energy, the increase of yields of symmetric products and the decrease of the peak-to-valley ( P/ V ratio in the 238U ( γ, f) reaction is similar to the 238U ( n, f) reaction. v) The increase of with excitation energy is also similar between the 238U ( γ, f ) and 238U ( n, f) reactions. However, it is surprising to see that the and values with excitation energy behave entirely differently from the 238U ( γ, f ) and 238U ( n, f ) reactions.

  2. Observation of new microsecond isomers among fission products of 345 MeV/nucleon 238U

    CERN Document Server

    Kameda, D; Ohnishi, T; Kusaka, K; Yoshida, A; Yoshida, K; Ohtake, M; Fukuda, N; Takeda, H; Tanaka, K; Inabe, N; Yanagisawa, Y; Gono, Y; Watanabe, H; Otsu, H; Baba, H; Ichihara, T; Yamaguchi, Y; Takechi, M; Nishimura, S; Ueno, H; Yoshimi, A; Sakurai, H; Motobayashi, T; Nakao, T; Mizoi, Y; Matsushita, M; Ieki, K; Kobayashi, N; Tanaka, K; Kawada, Y; Tanaka, N; Deguchi, S; Satou, Y; Kondo, Y; Nakamura, T; Yoshinaga, K; Ishii, C; Yoshii, H; Miyashita, Y; Uematsu, N; Shiraki, Y; Sumikama, T; Chiba, J; Ideguchi, E; Saito, A; Yamaguchi, T; Hachiuma, I; Suzuki, T; Moriguchi, T; Ozawa, A; Ohtsubo, T; Famiano, M A; Geissel, H; Nettleton, A S; Tarasov, O B; Bazin, D; Sherrill, B M; Manikonda, S L; Nolen, J A

    2012-01-01

    A search for isomeric gamma-decays among fission fragments from 345 MeV/nucleon 238U has been performed at the RIKEN Nishina Center RI Beam Factory. Fission fragments were selected and identified using the superconducting in-flight separator BigRIPS and were implanted in an aluminum stopper. Delayed gamma-rays were detected using three clover-type high-purity germanium detectors located at the focal plane within a time window of 20 microseconds following the implantation. We identified a total of 54 microsecond isomers with half-lives of ~0.1 - 10 microseconds, including discovery of 18 new isomers in very neutron-rich nuclei: 59Tim, 90Asm, 92Sem, 93Sem, 94Brm, 95Brm, 96Brm, 97Rbm, 108Nbm, 109Mom, 117Rum, 119Rum, 120Rhm, 122Rhm, 121Pdm, 124Pdm, 124Agm and 126Agm, and obtained a wealth of spectroscopic information such as half-lives, gamma-ray energies, gamma-ray relative intensities and gamma-gamma coincidences over a wide range of neutron-rich exotic nuclei. Proposed level schemes are presented for 59Tim, 82...

  3. Evaluation of correlating factors between {sup 238}U concentration measured in fine and course atmospheric particles

    Energy Technology Data Exchange (ETDEWEB)

    Peixoto, Claudia Marques; Jacomino, Vanusa Maria Feliciano; Barreto, Alberto Avelar; Dias, Vagner Silva, E-mail: cmp@cdtn.b, E-mail: vmfj@cdtn.b, E-mail: aab@cdtn.b [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil); Dias, Fabiana Ferrari, E-mail: fdias@cnen.gov.b [Brazilian Nuclear Energy Commission (CNEN-/MG), Pocos de Caldas, MG (Brazil). Lab. de Pocos de Caldas (LAPOC)

    2009-07-01

    Air quality is ever more important in function of the enormous proportion of human actions that have affected the environment over the last two centuries. Particulate material is one among many pollutants that can cause great risk to human health and the environment. It can be classified as: Total Suspended Particles (TSP), defined simply as particles with less than 50 mum aerodynamic diameter (one group of these particles can be inhaled and may cause health problems, while others may unfavorably affect the population's quality of life, interfering in environmental conditions and impairing normal community activities); and Inhalable Particles (PM{sub 10}), defined as those particles with less than 10 mum aerodynamic diameter. These particles penetrate the respiratory system and can reach pulmonary alveoli due to their small size, causing serious health damage. The Nuclear Technology Development Center (CDTN) has monitored air quality around its installations since 2000. CDTN's Environmental Monitoring Program (EMP) includes monitoring radioactivity levels contained in atmospheric TSP. In order to optimize its program, CDTN is carrying out a study to estimate the correlation between concentrations of particulate material measured in TSP and those measured in PM{sub 10}, PI{sub 2.5} and PI{sub 1}, as well as determination of activity concentration for each controlled radionuclide in all parts. The objective of this study is to present preliminary results and report {sup 238}U activity concentration results. (author)

  4. 230Th/238U dating of hydrothermal sulfides from Duanqiao hydrothermal field, Southwest Indian Ridge

    Science.gov (United States)

    Yang, Weifang; Tao, Chunhui; Li, Huaiming; Liang, Jin; Liao, Shili; Long, Jiangping; Ma, Zhibang; Wang, Lisheng

    2016-11-01

    Duanqiao hydrothermal field is located between the Indomed and Gallieni fracture zones at the central volcano, at 50°28'E in the ultraslow-spreading Southwest Indian Ridge (SWIR). Twenty-eight subsamples from a relict chimney and massive sulfides were dated using the 230Th/238U method. Four main episodes of hydrothermal activity were determined according to the restricted results: 68.9-84.3, 43.9-48.4, 25.3-34.8, and 0.7-17.3 kyrs. Hydrothermal activity of Duanqiao probably started about 84.3 (±0.5) kyrs ago and ceased about 0.737 (±0.023) kyrs ago. The periodic character of hydrothermal activity may be related to the heat source provided by the interaction of local magmatism and tectonism. The estimated mean growth rate of the sulfide chimney is Dragon Flag field is much more recent than that of Duanqiao or Mt. Jourdanne fields. The massive sulfides are younger than the sulfides from other hydrothermal fields such as Rainbow, Sonne and Ashadze-2. The preliminarily estimated reserves of sulfide ores of Duanqiao are approximately 0.5-2.9 million tons.

  5. 238U(n, γ reaction cross section measurement with C6D6 detectors at the n_TOF CERN facility.

    Directory of Open Access Journals (Sweden)

    Mingrone F.

    2014-03-01

    Full Text Available The radiative capture cross section of 238U is very important for the developing of new reactor technologies and the safety of existing ones. Here the preliminary results of the 238U(n,γ cross section measurement performed at n_TOF with C6D6 scintillation detectors are presented, paying particular attention to data reduction and background subtraction.

  6. Time-dependent Hartree-Fock calculations for multinucleon transfer and quasifission processes in $^{64}$Ni+$^{238}$U reaction

    CERN Document Server

    Sekizawa, Kazuyuki

    2016-01-01

    Background: Multinucleon transfer (MNT) and quasifission (QF) processes are dominant processes in low-energy collisions of two heavy nuclei. They are expected to be useful to produce neutron-rich unstable nuclei. Nuclear dynamics leading to these processes depends sensitively on nuclear properties such as deformation and shell structure. Purpose: We elucidate reaction mechanisms of MNT and QF processes involving heavy deformed nuclei, making detailed comparisons between microscopic TDHF calculations and measurements for $^{64}$Ni+$^{238}$U reaction. Methods: Three-dimensional Skyrme-TDHF calculations are performed. Particle-number projection method is used to evaluate MNT cross sections from the TDHF wave function after collision. Results: Fragment masses, total kinetic energy (TKE), scattering angle, contact time, and MNT cross sections are investigated for $^{64}$Ni+$^{238}$U reaction. They show reasonable agreements with measurements. At small impact parameters, collision dynamics depends sensitively on th...

  7. Measurement and analysis of the 238U(n, 2n) reaction rate in depleted uranium/polyethylene shells

    Institute of Scientific and Technical Information of China (English)

    YAN Xiao-Song; LIU Rong; LU Xin-Xin; JIANG Li; WEN Zhong-Wei; HAN Zi-Jie

    2012-01-01

    In order to check the conceptual design of the subcritical blanket in a fnsion-fission hybrid reactor,a depleted uranium/polyethylene simulation device with alternate shells has been established.The measurement of the 238U(n,2n) reaction rate was carried out using an activation technique,by measuring the 208 keV γ rays emitted from 237 U.The self-absorption of depleted uranium foils with different thicknesses was experimentally corrected.The distribution of the 238U(n,2n) reaction rate at 90° to the incident D+ beam was obtained,with uncertainty between 5.3% and 6.0%.The experiment was analyzed using MCNP5 code with the ENDF/BVI library,and the calculated results are all about 5% higher than the measured results.

  8. Angular distribution of fragments from neutron-induced fission of {sup 238}U in the intermediate energy region

    Energy Technology Data Exchange (ETDEWEB)

    Carlsson, Magnus

    2004-06-01

    Areas ranging from nuclear structure models to accelerator-driven systems benefit from improved neutron-induced fission data in the intermediate energy region. In this Master's degree thesis, the fragment angular distribution from fission of {sup 238}U, induced by 21-MeV neutrons, has been analysed from an experiment performed with the Medley/DIFFICILE setup at the The Svedberg Laboratory in Uppsala. The data have been corrected for low energy neutrons in the beam. The results agree with other experiments, as well as with model calculations. The data should be a starting point for further analysis with a goal to deduce the fission cross-section of {sup 238}U.

  9. Field analyses of (238)U and (226)Ra in two uranium mill tailings piles from Niger using portable HPGe detector.

    Science.gov (United States)

    Déjeant, Adrien; Bourva, Ludovic; Sia, Radia; Galoisy, Laurence; Calas, Georges; Phrommavanh, Vannapha; Descostes, Michael

    2014-11-01

    The radioactivities of (238)U and (226)Ra in mill tailings from the U mines of COMINAK and SOMAÏR in Niger were measured and quantified using a portable High-Purity Germanium (HPGe) detector. The (238)U and (226)Ra activities were measured under field conditions on drilling cores with 600s measurements and without any sample preparation. Field results were compared with those obtained by Inductive Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) and emanometry techniques. This comparison indicates that gamma-ray absorption by such geological samples does not cause significant deviations. This work shows the feasibility of using portable HPGe detector in the field as a preliminary method to observe variations of radionuclides concentration with the aim of identifying samples of interest. The HPGe is particularly useful for samples with strong secular disequilibrium such as mill tailings.

  10. Estimation of uncertainties in resonance parameters of {sup 56}Fe, {sup 239}Pu, {sup 240}Pu and {sup 238}U

    Energy Technology Data Exchange (ETDEWEB)

    Nakagawa, Tsuneo; Shibata, Keiichi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1997-05-01

    Uncertainties have been estimated for the resonance parameters of {sup 56}Fe, {sup 239}Pu, {sup 240}Pu and {sup 238}U contained in JENDL-3.2. Errors of the parameters were determined from the measurements which the evaluation was based on. The estimated errors have been compiled in the MF32 of the ENDF format. The numerical results are given in tables. (author)

  11. Fission Fragment Angular Distribution measurements of 235U and 238U at CERN n_TOF facility

    Directory of Open Access Journals (Sweden)

    Leal-Cidoncha E.

    2016-01-01

    In order to measure the FFAD of neutron-induced reactions, a fission detection setup based on parallel-plate avalanche counters (PPACs has been developed and successfully used at the CERN-n_TOF facility. In this work, we present the preliminary results on the analysis of new 235U(n,f and 238U(n,f data in the extended energy range up to 200 MeV compared to the existing experimental data.

  12. Investigation of fission properties and evaporation residue measurement in the reactions using 238U target nucleus

    Directory of Open Access Journals (Sweden)

    Saro S.

    2011-10-01

    Full Text Available Fragment mass distributions for fission after full momentum transfer were measured in the reactions of 30Si,34,36 S,31P,40Ar + 238U at bombarding energies around the Coulomb barrier. Mass distributions change significantly as a function of incident beam energy. The asymmetric fission probability increases at sub-barrier energy. The phenomenon is interpreted as an enhanced quasifission probability owing to orientation effects on fusion and/or quasifission. The evaporation residue (ER cross sections were measured in the reactions of 30Si + 238U and 34S + 238U to obtain information on fusion. In the latter reaction, significant suppression of fusion was implied. This suggests that fission events different from compound nucleus are included in the masssymmetric fragments. The results are supported by a model calculation based on a dynamical calculation using Langevin equation, in which the mass distribution for fusion-fission and quasifission fragments are separately determined.

  13. Radioactivity of Natural Nuclides (40K, 238U, 232Th, 226Ra in Coals from Eastern Yunnan, China

    Directory of Open Access Journals (Sweden)

    Xin Wang

    2015-09-01

    Full Text Available The naturally occurring primordial radionuclides in coals might exhibit high radioactivity, and can be exported to the surrounding environment during coal combustion. In this study, nine coal samples were collected from eastern Yunnan coal deposits, China, aiming at characterizing the overall radioactivity of some typical nuclides (i.e., 40K, 238U, 232Th, 226Ra and assessing their ecological impact. The mean activity concentrations of 238U, 232Th, 40K and 226Ra are 63.86 (17.70–92.30 Bq· kg-1, 23.76 (11.10–37.10 Bq· kg-1, 96.84 (30.60–229.30 Bq· kg-1 and 28.09 Bq·kg-1 (3.10–61.80 Bq·kg-1, respectively. Both 238U and 232Th have high correlations with ash yield of coals, suggesting their inorganic origins. The overall environmental effect of natural radionuclides in studied coals is considered to be negligible, as assessed by related indexes (i.e., radium equivalent activity, air-adsorbed dose rate, annual effective dose, and external hazard index. However, the absorbed dose rates values are higher than the average value of global primordial radiation and the Chinese natural gamma radiation dose rate.

  14. 238U/235U variations in meteorites: extant 247Cm and implications for Pb-Pb dating.

    Science.gov (United States)

    Brennecka, G A; Weyer, S; Wadhwa, M; Janney, P E; Zipfel, J; Anbar, A D

    2010-01-22

    The 238U/235U isotope ratio has long been considered invariant in meteoritic materials (equal to 137.88). This assumption is a cornerstone of the high-precision lead-lead dates that define the absolute age of the solar system. Calcium-aluminum-rich inclusions (CAIs) of the Allende meteorite display variable 238U/235U ratios, ranging between 137.409 +/- 0.039 and 137.885 +/- 0.009. This range implies substantial uncertainties in the ages that were previously determined by lead-lead dating of CAIs, which may be overestimated by several million years. The correlation of uranium isotope ratios with proxies for curium/uranium (that is, thorium/uranium and neodymium/uranium) provides strong evidence that the observed variations of 238U/235U in CAIs were produced by the decay of extant curium-247 to uranium-235 in the early solar system, with an initial 247Cm/235U ratio of approximately 1.1 x 10(-4) to 2.4 x 10(-4).

  15. Investigation of the 238U(d ,p ) surrogate reaction via the simultaneous measurement of γ -decay and fission probabilities

    Science.gov (United States)

    Ducasse, Q.; Jurado, B.; Aïche, M.; Marini, P.; Mathieu, L.; Görgen, A.; Guttormsen, M.; Larsen, A. C.; Tornyi, T.; Wilson, J. N.; Barreau, G.; Boutoux, G.; Czajkowski, S.; Giacoppo, F.; Gunsing, F.; Hagen, T. W.; Lebois, M.; Lei, J.; Méot, V.; Morillon, B.; Moro, A. M.; Renstrøm, T.; Roig, O.; Rose, S. J.; Sérot, O.; Siem, S.; Tsekhanovich, I.; Tveten, G. M.; Wiedeking, M.

    2016-08-01

    We investigated the 238U(d ,p ) reaction as a surrogate for the n +238U reaction. For this purpose we measured for the first time the γ -decay and fission probabilities of *239U simultaneously and compared them to the corresponding neutron-induced data. We present the details of the procedure to infer the decay probabilities, as well as a thorough uncertainty analysis, including parameter correlations. Calculations based on the continuum-discretized coupled-channels method and the distorted-wave Born approximation (DWBA) were used to correct our data from detected protons originating from elastic and inelastic deuteron breakup. In the region where fission and γ emission compete, the corrected fission probability is in agreement with neutron-induced data, whereas the γ -decay probability is much higher than the neutron-induced data. We have performed calculations of the decay probabilities with the statistical model and of the average angular momentum populated in the 238U(d ,p ) reaction with the DWBA to interpret these results.

  16. Solubility of {sup 238}U radionuclide from various types of soil in synthetic gastrointestinal fluids using “US in vitro” digestion method

    Energy Technology Data Exchange (ETDEWEB)

    Rashid, Nur Shahidah Abdul; Sarmani, Sukiman; Majid, Amran Ab.; Mohamed, Faizal; Siong, Khoo Kok, E-mail: khoo@ukm.edu.my [School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia (UKM), 43600 Bangi, Selangor (Malaysia)

    2015-04-29

    238U radionuclide is a naturally occuring radioactive material that can be found in soil. In this study, the solubility of 238U radionuclide obtained from various types of soil in synthetic gastrointestinal fluids was analysed by “US P in vitro” digestion method. The synthetic gastrointestinal fluids were added to the samples with well-ordered, mixed throughly and incubated according to the human physiology digestive system. The concentration of 238U radionuclide in the solutions extracted from the soil was measured using Induced Coupling Plasma Mass Spectrometer (ICP-MS). The concentration of 238U radionuclide from the soil samples in synthetic gastrointestinal fluids showed different values due to different homogenity of soil types and chemical reaction of 238U radionuclide. In general, the solubility of 238U radionuclide in gastric fluid was higher (0.050 – 0.209 ppm) than gastrointestinal fluids (0.024 – 0.050 ppm). It could be concluded that the US P in vitro digestion method is practicle for estimating the solubility of 238U radionuclide from soil materials and could be useful for monitoring and risk assessment purposes applying to environmental, health and contaminated soil samples.

  17. Annual committed effective dose from olive oil (due to 238U, 232Th, and 222Rn) estimated for members of the Moroccan public from ingestion and skin application.

    Science.gov (United States)

    Misdaq, M A; Touti, R

    2012-03-01

    Olive oil is traditionally refined and widely consumed by Moroccan rural populations. Uranium (238U), thorium (232Th), radon (222Rn), and thoron (220Rn) contents were measured in various locally produced olive oil samples collected in rural areas of Morocco. These radionuclides were also measured inside various bottled virgin olive oils consumed by the Moroccan populations. CR-39 and LR-115 type II solid state nuclear track detectors (SSNTDs) were used. Annual committed effective doses due to 238U, 232Th, and 222Rn from the ingestion of olive oil by the members of the general public were determined. The maximum total committed effective dose due to 238U, 232Th, and 222Rn from the ingestion of olive oil by adult members of Moroccan rural populations was found equal to 5.9 µSv y-1. The influence of pollution due to building material dusts and phosphates on the radiation dose to workers from the ingestion of olive oil was investigated, and it was found that the maximum total committed effective dose due to 238U, 232Th, and 222Rn was on the order of 0.22 mSy y-1. Committed effective doses to skin due to 238U, 232Th, and 222Rn from the application of olive oil masks by rural women were evaluated. The maximum total committed effective dose to skin due to 238U, 232Th, and 222Rn was found equal to 0.07 mSy y-1 cm-2.

  18. 238U-230Th dating of chevkinite in high-silica rhyolites from La Primavera and Yellowstone calderas

    Science.gov (United States)

    Vazquez, Jorge A.; Velasco, Noel O.; Schmitt, Axel K.; Bleick, Heather A.; Stelten, Mark E.

    2014-01-01

    Application of 238U-230Th disequilibrium dating of accessory minerals with contrasting stabilities and compositions can provide a unique perspective on magmatic evolution by placing the thermochemical evolution of magma within the framework of absolute time. Chevkinite, a Th-rich accessory mineral that occurs in peralkaline and metaluminous rhyolites, may be particularly useful as a chronometer of crystallization and differentiation because its composition may reflect the chemical changes of its host melt. Ion microprobe 128U-230Th dating of single chevkinite microphenocrysts from pre- and post-caldera La Primavera, Mexico, rhyolites yields model crystallization ages that are within 10's of k.y. of their corresponding K-Ar ages of ca. 125 ka to 85 ka, while chevkinite microphenocrysts from a post-caldera Yellowstone, USA, rhyolite yield a range of ages from ca. 110 ka to 250 ka, which is indistinguishable from the age distribution of coexisting zircon. Internal chevkinite-zircon isochrons from La Primavera yield Pleistocene ages with ~5% precision due to the nearly two order difference in Th/U between both minerals. Coupling chevkinite 238U-230Th ages and compositional analyses reveals a secular trend of Th/U and rare earth elements recorded in Yellowstone rhyolite, likely reflecting progressive compositional evolution of host magma. The relatively short timescale between chevkinite-zircon crystallization and eruption suggests that crystal-poor rhyolites at La Primavera were erupted shortly after differentiation and/or reheating. These results indicate that 238U-230Th dating of chevkinite via ion microprobe analysis may be used to date crystallization and chemical evolution of silicic magmas.

  19. Probing the role of Skyrme interactions on the fission dynamics of the 6Li + 238U reaction

    Science.gov (United States)

    Sharma, Ishita; Kumar, Raj; Sharma, Manoj K.

    2017-06-01

    The performance of selected five Skyrme forces (out of a set of 240), tested by Dutra et al., is analyzed in view of fusion-fission dynamics. These forces are assumed to perform better for neutron-rich systems, so the choice of the reaction is accordingly made by opting for a neutron-rich target in 6Li + 238U reaction. This reaction is diagnosed further in reference to fusion hindrance within the dynamical approach of the cluster-decay model (DCM). In order to reduce the computational time, three Skyrme forces are figured out with the criteria that these forces cover the barrier characteristics of the remaining two forces as well. The fission cross-sections are successfully addressed at low energies for the 6Li + 238U reaction. However, at relatively higher energies, the excitation functions show theoretical suppression with respect to experimental data, which may be associated with the possible existence of incomplete fusion (ICF). For ICF, we have considered that the 6Li broke into 4He + 2H, as mentioned in the experimental work. The calculations of ICF are carried out for the 4He + 238U reaction with the selected Skyrme forces at E_{c.m.} = 26.20 and 27.51 MeV. These forces address the data nicely for the compound nucleus (CN) as well as ICF processes. Here, the NRAPR force seems to require lesser barrier modification as compared to the other forces, therefore it can be used as an alternate choice for calculating the interaction potential. Additionally, the prediction of cross-sections at lower energies has been done with DCM using the NRAPR force. The ℓ-dependent % barrier modification of the Skyrme forces undertaken is also worked out in reference to fusion hindrance at below barrier energies.

  20. Multi-modal calculations of prompt fission neutrons from 238U(n, f) at low induced energy

    Institute of Scientific and Technical Information of China (English)

    ZHENG Na; ZHONG Chun-Lai; FAN Tie-Shuan

    2011-01-01

    Properties of prompt fission neutrons from 238U(n,f) are calculated for incident neutron energies below 6 MeV using the multi-modal model,including the prompt fission neutron spectrum,the average prompt fission neutron multiplicity,and the prompt fission neutron multiplicity as a function of the fission fragment mass v(A) (usually named “sawtooth” data) The three most dominant fission modes are taken into account.The model parameters are determined on the basis of experimental fission fragment data.The predicted results are in good agreement with the experimental data.

  1. Fragment properties from fission of {sup 234,238}U induced by 6 -10 MeV bremsstrahlung

    Energy Technology Data Exchange (ETDEWEB)

    Goeoek, Alf; Eckardt, Christian; Enders, Joachim; Freudenberger, Martin; Neumann-Cosel, Peter von [Institut fuer Kernphysik, Technische Universitaet Darmstadt (Germany); Hambsch, Franz-Josef; Oberstedt, Stephan [EC-JRC IRMM, Geel (Belgium); Oberstedt, Andreas [Akademi foer Naturvetenskap och Teknik, Oerebro Universitet (Sweden); Fundamental Fysik, Chalmers Tekniska Hoegskola, Goeteborg (Sweden); Richter, Achim [Institut fuer Kernphysik, Technische Universitaet Darmstadt (Germany); ECT, Villazzano (Trento) (Italy)

    2012-07-01

    Experiments to investigate the photon-induced fission of actinide nuclei at excitation energies in the vicinity of the fission barrier are carried out at the super conducting Darmstadt linear electron accelerator S-DALINAC. A twin Frisch grid ionization chamber is used to deduce mass, total kinetic energy, and angular distributions of the fission fragments. In this contribution results on fission fragment mass and total kinetic energy distributions from {sup 234,238}U are presented along with the currently on-going investigation of {sup 234}U and {sup 232}Th fragment angular distributions.

  2. 206Pb-230Th-234U-238U and 207Pb-235U geochronology of Quaternary opal, Yucca Mountain, Nevada

    Science.gov (United States)

    Neymark, Leonid A.; Amelin, Yuri V.; Paces, James B.

    2000-01-01

    U–Th–Pb isotopic systems have been studied in submillimeter-thick outermost layers of Quaternary opal occurring in calcite–silica fracture and cavity coatings within Tertiary tuffs at Yucca Mountain, Nevada, USA. These coatings preserve a record of paleohydrologic conditions at this site, which is being evaluated as a potential high-level nuclear waste repository. The opal precipitated from groundwater is variably enriched in 234U (measured 234U/238U activity ratio 1.124–6.179) and has high U (30–313 ppm), low Th (0.008–3.7 ppm), and low common Pb concentrations (measured 206Pb/204Pb up to 11,370). It has been demonstrated that the laboratory acid treatment used in this study to clean sample surfaces and to remove adherent calcite, did not disturb U–Th–Pb isotopic systems in opal. The opal ages calculated from 206Pb∗/238U and 207Pb∗/235U ratios display strong reverse discordance because of excess radiogenic 206Pb∗ derived from the elevated initial 234U. The data are best interpreted using projections of a new four-dimensional concordia diagram defined by 206Pb∗/238U, 207Pb∗/235U, 234U/238Uactivity, and 230Th/238Uactivity. Ages and initial 234U/238U activity ratios have been calculated using different projections of this diagram and tested for concordance. The data are discordant, that is observed 207Pb∗/235U ages of 170 ± 32 (2σ) to 1772 ± 40 ka are systematically older than 230Th/U ages of 34.1 ± 0.6 to 452 ± 32 ka. The age discordance is not a result of migration of uranium and its decay products under the open system conditions, but a consequence of noninstantaneous growth of opal. Combined U–Pb and 230Th/U ages support the model of slow mineral deposition at the rates of millimeters per million years resulting in layering on a scale too fine for mechanical sampling. In this case, U–Pb ages provide more accurate estimates of the average age for mixed multiage samples than 230Th/U ages, because ages based on shorter

  3. Gamma Emission Spectra from Neutron Resonances in 234,236,238U Measured Using the Dance Detector at Lansce

    Science.gov (United States)

    Ullmann, J. L.; Bredeweg, T. A.; Couture, A. J.; Haight, R. C.; Jandel, M.; Kawano, T.; Keksis, A. L.; O'Donnell, J. M.; Rundberg, R. S.; Vieira, D. J.; Wouters, J. M.; Wilhelmy, J. B.; Wu, C. Y.; Becker, J. A.; Chyzh, A.; Baramsai, B.; Mitchell, G. E.; Krticka, M.

    2013-03-01

    An accurate knowledge of the radiative strength function and level density is needed to calculate of neutron-capture cross sections. An additional constraint on these quantities is provided by measurements of γ-ray emission spectra following capture. We present γ-emission spectra from several neutron resonances in 234,236,238U, measured using the DANCE detector at LANSCE. The measurements are compared to preliminary calculations of the cascade. It is observed that the generalized Lorentzian form of the E1 strength function cannot reproduce the shape of the emission spectra, but a better description is made by adding low-lying M1 Lorentzian strength.

  4. Determination of specific concentrations of {sup 40}K, {sup 238}U and {sup 232}Th in mineral fertilizer samples

    Energy Technology Data Exchange (ETDEWEB)

    Garcez, Ricardo W.D.; Lopes, Jose M.; Silva, Ademir X., E-mail: r.w.o.g@fisica.if.uff.br, E-mail: ademir@nuclear.ufrj.br [Coordenacao dos Programas de Pos-Graduacao em Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Programa de Engenharia Nuclear; Domingues, Alessandro M.; Lima, Marco F. [Universidade Federal Fluminense (UFF), Niteroi, RJ (Brazil)

    2015-07-01

    The use of fertilizer is an established practice worldwide to promote agricultural productivity increased without increasing the planted area, resulting in native forests protection and increase of the food availability. Some kinds of fertilizer have in their chemical composition some radionuclides due the origin of its feedstock, such as {sup 238}U, the {sup 232}Th, and their descendants, beyond {sup 40}K. Knowledge of the radioactivity levels in the environment is great importance to know the gamma radiation dose that the human being is exposed. For identification and quantitation of radionuclides, it was used gamma spectrometry where HPGe detector was used to obtain the spectra, and LabSOCS software for calculating the detection efficiency for each energy. The values of {sup 232}Th specific concentrations ranged from 4.1 to 368.1 Bq.Kg{sup -1}, the values of {sup 238}U specific concentrations ranged from 16.0 to 647.7 Bq.Kg{sup -1} and {sup 40}K specific concentrations ranged from 19.1 to 12713 Bq.Kg{sup -1}. Concentrations of values are consistent with those found in literature. (author)

  5. Uranium concentrations and 234U/238U activity ratios in fault-associated groundwater as possible earthquake precursors

    Science.gov (United States)

    Finkel, R. C.

    In order to assess the utility of uranium isotopes as fluid phase earthquake precursors, uranium concentrations and 234U/238U activity ratios have been monitored on a monthly or bimonthly basis in water from 24 wells and springs associated with Southern California fault zones. Uranium concentrations vary from 0.002 ppb at Indian Canyon Springs on the San Jacinto fault to 8.3 ppb at Lake Hughes well on the San Andreas fault in the Palmdale area. 234U/238U activity ratios vary from 0.88 at Agua Caliente Springs on the Elsinore fault to 5.4 at Niland Slab well on the San Andreas fault in the Imperial Valley. There was one large earthquake in the study area during 1979, the 15 October 1979 M=6.6 Imperial Valley earthquake. Correlated with this event, uranium concentrations varied by a factor of more than 60 and activity ratios by a factor of 3 at the Niland Slab site, about 70 km from the epicenter. At the other sites monitored, uranium concentrations varied in time, but with no apparent pattern, while uranium activity ratios remained essentially constant throughout the monitoring period.

  6. Primordial radioactivity ((238)U, (232)Th and (40)K) measurements for soils of Ludhiana district of Punjab, India.

    Science.gov (United States)

    Badhan, K; Mehra, R

    2012-11-01

    The aim of the present work was to study the activity concentration and absorbed gamma dose rates due to primordial radionuclides ((238)U, (232)Th and (40)K) for the soil of different villages of Ludhiana district of Punjab, India using a high-purity germanium detector based on high resolution gamma-ray spectrometry. The average activity concentrations of (238)U, (232)Th and (40)K in the soil samples have been found to be 28.58, 50.95 and 569.59 Bq kg(-1), respectively, which gives the total gamma dose rate contribution of 68.50 nGy h(-1). To evaluate the radiological hazard of the natural radioactivity, the radium equivalent activity, the external hazard index, the absorbed dose rate and the effective dose rate have been calculated. The calculated radium equivalent activity values are on the lower side of the recommended safe limit value of 370 Bq kg(-1) by Organization of Economic and Control Department. The calculated value of external health hazard index is lower than unity.

  7. Photofission product yields of {sup 238}U and {sup 239}Pu with 22-MeV bremsstrahlung

    Energy Technology Data Exchange (ETDEWEB)

    Wen, Xianfei; Yang, Haori, E-mail: haori.yang@oregonstate.edu

    2016-06-11

    In homeland security and nuclear safeguards applications, non-destructive techniques to identify and quantify special nuclear materials are in great demand. Although nuclear materials naturally emit characteristic radiation (e.g. neutrons, γ-rays), their intensity and energy are normally low. Furthermore, such radiation could be intentionally shielded with ease or buried in high-level background. Active interrogation techniques based on photofission have been identified as effective assay approaches to address this issue. In designing such assay systems, nuclear data, like photofission product yields, plays a crucial role. Although fission yields for neutron-induced reactions have been well studied and readily available in various nuclear databases, data on photofission product yields is rather scarce. This poses a great challenge to the application of photofission techniques. In this work, short-lived high-energy delayed γ-rays from photofission of {sup 238}U were measured in between linac pulses. In addition, a list-mode system was developed to measure relatively long-lived delayed γ-rays from photofission of {sup 238}U and {sup 239}Pu after the irradiation. Time and energy information of each γ-ray event were simultaneously recorded by this system. Cumulative photofission product yields were then determined using the measured delayed γ-ray spectra.

  8. Spectral interference corrections for the measurement of (238)U in materials rich in thorium by a high resolution gamma-ray spectrometry.

    Science.gov (United States)

    Yücel, H; Solmaz, A N; Köse, E; Bor, D

    2009-11-01

    In this study, the spectral interferences are investigated for the analytical peaks at 63.3 keV of (234)Th and 1001.0 keV of (234m)Pa, which are often used in the measurement of (238)U activity by the gamma-ray spectrometry. The correction methods are suggested to estimate the net peak areas of the gamma-rays overlapping the analytical peaks, due to the contribution of (232)Th that may not be negligible in materials rich in natural thorium. The activity results for the certified reference materials (CRMs) containing U and Th were measured with a well type Ge detector. The self-absorption and true coincidence-summing (TCS) effects were also taken into account in the measurements. It is found that ignoring the contributions of the interference gamma-rays of (232)Th and (235)U to the mixed peak at 63.3 keV of (234)Th ((238)U) leads to the remarkably large systematic influence of 0.8-122% in the measured (238)U activity, but in case of ignoring the contribution of (232)Th via the interference gamma-ray at 1000.7 keV of (228)Ac to the mixed peak at 1001 keV of (234m)Pa ((238)U) results in relatively smaller systematic influence of 0.05-3%, depending on thorium contents in the samples. The present results showed that the necessary correction for the spectral interferences besides self-absorption and TCS effects is also very important to obtain more accurate (238)U activity results. Additionally, if one ignores the contribution of (232)Th to both (238)U and (40)K activities in materials, the maximum systematic influence on the effective radiation dose is estimated to be ~6% and ~1% via the analytical peaks at 63.3 and 1001 keV for measurement of the (238)U activity, respectively.

  9. The transport characteristics of {sup 238}U, {sup 232}Th, {sup 226}Ra, and {sup 40}K in the production cycle of phosphate rock

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Yoon Hee; Lim, Jong Myoung; Ji, Young Yong; Chung, Kun Ho; Kang, Mun Ja [Environmental Radioactivity Assessment Team, Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2017-03-15

    Phosphate rock and its by-product are widely used in various industries to produce phosphoric acid, gypsum, gypsum board, and fertilizer. Owing to its high level of natural radioactive nuclides (e.g., 238U and 226Ra), the radiological safety of workers who work with phosphate rock should be systematically managed. In this study, 238U, 232Th, 226Ra, and 40K levels were measured to analyze the transport characteristics of these radionuclides in the production cycle of phosphate rock. Energy dispersive X-ray fluorescence and gamma spectrometry were used to determine the activity of 238U, 232Th, 226Ra, and 40K. To evaluate the extent of secular disequilibrium, the analytical results were compared using statistical methods. Finally, the distribution of radioactivity across different stages of the phosphate rock production cycle was evaluated. The concentration ratios of 226Ra and 238U in phosphate rock were close to 1.0, while those found in gypsum and fertilizer were extremely different, reflecting disequilibrium after the chemical reaction process. The nuclide with the highest activity level in the production cycle of phosphate rock was 40K, and the median 40K activity was 8.972 Bq·g−1 and 1.496 Bq·g−1, respectively. For the 238U series, the activity of 238U and 226Ra was greatest in phosphate rock, and the distribution of activity values clearly showed the transport characteristics of the radionuclides, both for the byproducts of the decay sequences and for their final products. Although the activity of 40K in k-related fertilizer was relatively high, it made a relatively low contribution to the total radiological effect. However, the activity levels of 226Ra and 238U in phosphate rock were found to be relatively high, near the upper end of the acceptable limits. Therefore, it is necessary to systematically manage the radiological safety of workers engaged in phosphate rock processing.

  10. Trace metal cycling and 238U/235U in New Zealand's fjords: Implications for reconstructing global paleoredox conditions in organic-rich sediments

    Science.gov (United States)

    Hinojosa, Jessica L.; Stirling, Claudine H.; Reid, Malcolm R.; Moy, Christopher M.; Wilson, Gary S.

    2016-04-01

    Reconstructing the history of ocean oxygenation provides insight into links between ocean anoxia, biogeochemical cycles, and climate. Certain redox-sensitive elements respond to changes in marine oxygen content through phase shifts and concomitant isotopic fractionation, providing new diagnostic proxies of past ocean hypoxia. Here we explore the behavior and inter-dependence of a suite of commonly utilized redox-sensitive trace metals (U, Mo, Fe, and Mn) and the emerging "stable" isotope system of U (238U/235U, or δ238U) in New Zealand fjords. These semi-restricted basins have chemical conditions spanning the complete redox spectrum from fully oxygenated to suboxic to intermittently anoxic/euxinic. In the anoxic water column, U and Mo concentrations decrease, while Fe and Mn concentrations increase. Similarly, signals of past euxinic conditions can be found by U, Mo, Fe, and Mn enrichment in the underlying sediments. The expected U isotopic shift toward a lower δ238U in the anoxic water column due to U(VI)-U(IV) reduction is not observed; instead, water column δ238U profiles are consistent in fjords of all oxygen content, falling within previously reported ranges for open ocean seawater (δ238U = -0.42 ± 0.07‰). Additionally, surface sediment δ238U results show evidence for competing U isotope fractionation processes. One site indicates increased export of 238U from seawater to the underlying sediments (fractionation between aqueous seawater U and particulate sediment U, or ΔU(aq)-U(solid) = -0.25‰), consistent with redox-driven fractionation. Another site suggests potential U(VI) adsorption-driven fractionation, reflecting increased export of 235U from seawater to sediments (ΔU(aq)-U(solid) = 0.25‰). We discuss several potential factors that could alter δ238U in waters and sediments beyond redox-driven shifts, including adsorption to organic matter in waters of high primary productivity, reaction rates for competing processes of U adsorption and

  11. Study of 236U/238U ratio at CIRCE using a 16-strip silicon detector with a TOF system

    Directory of Open Access Journals (Sweden)

    De Cesare M.

    2015-01-01

    Full Text Available Accelerator Mass Spectrometry (AMS is presently the most sensitive technique for the measurement of long-lived actinides, e.g. 236U and xPu isotopes. A new actinide AMS system, based on a 3-MV pelletron tandem accelerator, is operated at the Center for Isotopic Research on Cultural and Environmental Heritage (CIRCE in Caserta, Italy. In this paper we report on the procedure adopted to increase the 236U abundance sensitivity as low as possible. The energy and position determinations of the 236U ions, using a 16-strip silicon detector have been obtained. A 236U/238U isotopic ratio background level of about 2.9×10−11 was obtained, summing over all the strips, using a Time of Flight-Energy (TOF-E system with a 16-strip silicon detector (4.9×10−12 just with one strip.

  12. Symmetric splitting for the system /sup 32/S+/sup 238/U at energies near and below the barrier

    Energy Technology Data Exchange (ETDEWEB)

    Freifelder, R.; Braun-Munzinger, P.; DeYoung, P.; Schicker, R.; Sen, S.; Stachel, J.

    1987-06-01

    The total capture cross section for the system /sup 32/S+/sup 238/U has been measured at energies from 0.93 to 1.08 times the s-wave interaction barrier by detecting coincident fission fragments following full momentum transfer reactions. The subbarrier cross section cannot be reproduced by a one-dimensional barrier penetration model. Using a quantum mechanical coupled channels model, good agreement is obtained. The measured angular distributions of fission fragments were compared to the predictions of saddle and scission point transition state theory. Saddle point transition state model calculations fail to reproduce the data, while scission point transition state calculations are in agreement with their qualitative trend. Evidence for nonequilibrium processes is presented.

  13. Isotopic Yield Distributions of Transfer- and Fusion-Induced Fission from 238U+12C Reactions in Inverse Kinematics

    CERN Document Server

    Caamaño, M; Farget, F; Derkx, X; Schmidt, K -H; Audouin, L; Bacri, C -O; Barreau, G; Benlliure, J; Casarejos, E; Chbihi, A; Fernandez-Dominguez, B; Gaudefroy, L; Golabek, C; Jurado, B; Lemasson, A; Navin, A; Rejmund, M; Roger, T; Shrivastava, A; Schmitt, C

    2013-01-01

    A novel method to access the complete identification in atomic number Z and mass A of fragments produced in low-energy fission of actinides is presented. This method, based on the use of multi- nucleon transfer and fusion reactions in inverse kinematics, is applied in this work to reactions between a 238U beam and a 12C target to produce and induce fission of moderately excited actinides. The fission fragments are detected and fully identified with the VAMOS spectrometer of GANIL, allowing the measurement of fragment yields of several hundreds of isotopes in a range between A ~ 80 and ~ 160, and from Z ~ 30 to ~ 64. For the first time, complete isotopic yield distributions of fragments from well-defined fissioning systems are available. Together with the precise measurement of the fragment emission angles and velocities, this technique gives further insight into the nuclear-fission process.

  14. Polonium 210Po, uranium (234U, 238U and plutonium (238Pu, 239+240Pu bioaccumulation in marine birds

    Directory of Open Access Journals (Sweden)

    Strumińska-Parulska D. I.

    2013-04-01

    Full Text Available The aim of this work was the determination of 210Po, 234U, 238U, 238Pu and 239+240Pu concentration in marine birds which permanently or temporally live in the southern Baltic Sea coast. We chose 11 species of seabirds: three species permanently residing at southern Baltic Sea, four species of wintering birds and three species of migrating birds. The results show that analyzed radionuclides are non-uniformly distributed in the marine birds. The highest activities of 210Po were observed in feathers, muscles and liver. The highest uranium content was found in liver, rest of viscera and feathers, while plutonium in the digestion organs and feathers. Omnivore seabirds accumulated more polonium, plutonium than species that feed on fish, while herbivore seabirds accumulated more uranium than carnivore.

  15. The estuarine chemistry and isotope systematics of 234,238U in the Amazon and Fly Rivers

    Science.gov (United States)

    Swarzenski, P.; Campbell, P.; Porcelli, D.; McKee, B.

    2004-01-01

    Natural concentrations of 238U and ??234U values were determined in estuarine surface waters and pore waters of the Amazon and Fly (Papua New Guinea) Rivers to investigate U transport phenomena across river-dominated land-sea margins. Discharge from large, tropical rivers is a major source of dissolved and solid materials transported to the oceans, and are important in defining not only oceanic mass budgets, but also terrestrial weathering rates. On the Amazon shelf, salinity-property plots of dissolved organic carbon, pH and total suspended matter revealed two vastly contrasting water masses that were energetically mixed. In this mixing zone, the distribution of uranium was highly non-conservative and exhibited extensive removal from the water column. Uranium removal was most pronounced within a salinity range of 0-16.6, and likely the result of scavenging and flocculation reactions with inorganic (i.e., Fe/Mn oxides) and organic colloids/particles. Removal of uranium may also be closely coupled to exchange and resuspension processes at the sediment/water interface. An inner-shelf pore water profile indicated the following diagenetic processes: extensive (???1 m) zones of Fe(III) - and, to a lesser degree, Mn(IV) - reduction in the absence of significant S(II) concentrations appeared to facilitate the formation of various authigenic minerals (e.g., siderite, rhodocrosite and uraninite). The pore water dissolved 238U profile co-varied closely with Mn(II). Isotopic variations as evidenced in ??234U pore waters values from this site revealed information on the origin and history of particulate uranium. Only after a depth of about 1 m did the ??234U value approach unity (secular equilibrium), denoting a residual lattice bound uranium complex that is likely an upper-drainage basin weathering product. This suggests that the enriched ??234U values represent a riverine surface complexation product that is actively involved in Mn-Fe diagenetic cycles and surface

  16. Coupling groundwater residence time and 234U/238U isotopic ratios in a granitic catchment (Vosges, Eastern France)

    Science.gov (United States)

    Viville, Daniel; Aquilina, Luc; Ackerer, Julien; Chatton, Eliot; Labasque, Thierry; Pierret, Marie-Claire; Granet, Mathieu; Perrone, Thierry; Chabaux, François

    2016-04-01

    Weathering processes are active in surface waters but groundwater also represents no neglectable chemical fluxes. As residence-time in groundwater are high, silicate weathering might take place and control Si, Ca and C fluxes. Weathering processes can be deduced from U isotopic ratios but the kinetics of these processes remain relatively poorly constrained. In order to better characterize these processes, we have coupled residence-times deduced from anthropogenic gases (CFC and SF6) analysis and 234U/238U isotopic ratios determination. Samples were collected in the Strengbach catchment (Hydro-geochemical Observatory OHGE, Vosges, eastern France). Two campaigns were carried out in May and August 2015 during two highly contrasted hydro-climatic periods. Both springs and boreholes down to 80 m depth have been sampled. A very clear geochemical distinction is observed between groundwater from surface springs and deeper groundwater from boreholes. Springs show much lower residence-time (few years) and specific chemical composition. Deeper groundwater have residence-time of several decades and different geochemical composition. A clear SF6 production is observed with increasing SF6 concentrations with residence-time. The campaign of May is characterized by highly groundwater levels and spring fluxes. All groundwater show very low residence time, except in the boreholes at depth greater than 40 m. Conversely, during low groundwater-level period in August, the residence times are much higher and CFC concentrations indicate a large mixing process between surface groundwater and deeper levels. The 234U/238U isotopic ratios confirm this vertical zonation in the boreholes, with much higher activity ratios in the deep ground-waters from borehole than in the surface and spring waters; Such high U activity ratios are indicative of long water-rock interactions, which is consistent with the long residence times deducted from the CFC and SF6 data.

  17. Reactive transport of uranium in a groundwater bioreduction study: Insights from high-temporal resolution 238U/235U data

    Science.gov (United States)

    Shiel, A. E.; Johnson, T. M.; Lundstrom, C. C.; Laubach, P. G.; Long, P. E.; Williams, K. H.

    2016-08-01

    We conducted a detailed investigation of U isotopes in conjunction with a broad geochemical investigation during field-scale biostimulation and desorption experiments. This investigation was carried out in the uranium-contaminated alluvial aquifer of the Rifle field research site. In this well-characterized setting, a more comprehensive understanding of U isotope geochemistry is possible. Our results indicate that U isotope fractionation is consistently observed across multiple experiments at the Rifle site. Microbially-mediated reduction is suggested to account for most or all of the observed fractionation as abiotic reduction has been demonstrated to impart much smaller, often near-zero, isotopic fractionation or isotopic fractionation in the opposite direction. Data from some time intervals are consistent with a simple model for transport and U(VI) reduction, where the fractionation factor (ε = +0.65‰ to +0.85‰) is consistent with experimental studies. However, during other time intervals the observed patterns in our data indicate the importance of other processes in governing U concentrations and 238U/235U ratios. For instance, we demonstrate that departures from Rayleigh behavior in groundwater systems arise from the presence of adsorbed species. We also show that isotope data are sensitive to the onset of oxidation after biostimulation ends, even in the case where reduction continues to remove contaminant uranium downstream. Our study and the described conceptual model support the use of 238U/235U ratios as a tool for evaluating the efficacy of biostimulation and potentially other remedial strategies employed at Rifle and other uranium-contaminated sites.

  18. Fission Product Yield Study of 235U, 238U and 239Pu Using Dual-Fission Ionization Chambers

    Science.gov (United States)

    Bhatia, C.; Fallin, B.; Howell, C.; Tornow, W.; Gooden, M.; Kelley, J.; Arnold, C.; Bond, E.; Bredeweg, T.; Fowler, M.; Moody, W.; Rundberg, R.; Rusev, G.; Vieira, D.; Wilhelmy, J.; Becker, J.; Macri, R.; Ryan, C.; Sheets, S.; Stoyer, M.; Tonchev, A.

    2014-05-01

    To resolve long-standing differences between LANL and LLNL regarding the correct fission basis for analysis of nuclear test data [M.B. Chadwick et al., Nucl. Data Sheets 111, 2891 (2010); H. Selby et al., Nucl. Data Sheets 111, 2891 (2010)], a collaboration between TUNL/LANL/LLNL has been established to perform high-precision measurements of neutron induced fission product yields. The main goal is to make a definitive statement about the energy dependence of the fission yields to an accuracy better than 2-3% between 1 and 15 MeV, where experimental data are very scarce. At TUNL, we have completed the design, fabrication and testing of three dual-fission chambers dedicated to 235U, 238U, and 239Pu. The dual-fission chambers were used to make measurements of the fission product activity relative to the total fission rate, as well as for high-precision absolute fission yield measurements. The activation method was employed, utilizing the mono-energetic neutron beams available at TUNL. Neutrons of 4.6, 9.0, and 14.5 MeV were produced via the 2H(d,n)3He reaction, and for neutrons at 14.8 MeV, the 3H(d,n)4He reaction was used. After activation, the induced γ-ray activity of the fission products was measured for two months using high-resolution HPGe detectors in a low-background environment. Results for the yield of seven fission fragments of 235U, 238U, and 239Pu and a comparison to available data at other energies are reported. For the first time results are available for neutron energies between 2 and 14 MeV.

  19. Determination of {sup 238}U and {sup 232}Th in geological samples by alpha and gamma spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Farias, Emerson E.G. de; Hazin, Clovis A., E-mail: chazin@cnen.gov.br [Universidade Federal de Pernambuco (UFPE), Recife, PE (Brazil). Dept. de Energia Nuclear; Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil); Honorato, Eliane V.; Franca, Elvis J. De, E-mail: valentim@cnen.gov.br, E-mail: ejfranca@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil)

    2011-07-01

    Alpha and gamma spectrometry are analytical techniques of great importance for the determination of natural radionuclides, especially for radioisotopes of the {sup 238}U and {sup 232}Th series. Due to the presence of completely different chemical elements in these series, with different gamma-ray abundances and decay branches, it is quite relevant to define consistent analytical approaches to be adopted in an environmental analysis routine basis. For the establishment of such protocol for the radiometric analysis of geological samples routinely analyzed in the Environmental Monitoring Division of the Northeastern Regional Center for Nuclear Sciences (CRCN-NE), reference materials of different geologic matrices prepared by the International Atomic Energy Agency - IAEA were analyzed through high resolution gamma-ray spectrometry by means of a Hyper Pure Germanium (HPGe) detector and high resolution alpha spectrometry using a surface barrier detector. Test portions of 2.5 g (for alpha analysis) and 50.0 g (for gamma analysis) of the reference materials IAEA-312 (soil), IAEA-314 (stream sediment), IAEA-375 (soil), and IAEA-135 (sea sediment) were analyzed. The concordance between the obtained values and the reference values for the specific activities of {sup 238}U and {sup 232}Th determined in the certified materials was considered quite satisfactory for both analytical techniques, since the relative errors were lower than 20 %, except for the results of gamma spectrometry using the line 93 keV, in which interference from the 93,35 keV gamma line of {sup 228}Ac (from the {sup 232}Th series) was detected. The results indicated a good degree of comparability for the radiometric analysis of geological samples. (author)

  20. The dissolved uranium concentration and (234)U/(238)U activity ratio in groundwaters from spas of southeastern Brazil.

    Science.gov (United States)

    Bonotto, Daniel Marcos

    2017-01-01

    This paper describes the natural radioactivity due to (238)U and (234)U in 75 water sources from spas located in 14 municipalities in São Paulo and Minas Gerais states, Brazil. These waters are extensively utilized for drinking in public places, bottling and bathing purposes, among other uses. The water samples were taken from springs and pumped tubular wells drilled into different aquifer systems in the Paraná and Southeastern Shield hydrogeological provinces. The measurements of alpha-emitting radionuclides were also accompanied by the monitoring of temperature, pH, Eh, electrical conductivity, dissolved gases (O2, CO2, H2S, radon, thoron) and major constituents. The dissolved U concentration data were lognormally distributed. The median and mean values corresponded to 0.02 and 0.09 μg/L, respectively. Significant relationships were found among the (234)U/(238)U activity ratio (AR) of dissolved uranium, the total dissolved solids (TDS) and dissolved bicarbonate contents, and also between the AR and dissolution rate in the monitored sites. The logU versus AR diagram used for the hydrogeochemical prospecting of concealed U deposits indicated that the water sources were mainly from reduced environments. The possibility of using the reciprocal of the dissolved U concentration and AR data to determine mixing volumes of different groundwater masses was demonstrated. The highest dissolved U concentration (4.82 μg/L) was well below the maximum allowed by WHO. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Extreme fractionation of 234U /238U and 230Th /234U in spring waters, sediments, and fossils at the Pomme de Terre Valley, southwestern Missouri

    Science.gov (United States)

    Szabo, Barney J.

    1982-09-01

    Isotopic fractionation as great as 1600% exists between 234U and 238U in spring waters, sediments, and fossils in the Pomme de Terre Valley, southwestern Missouri. The activity ratios of 234U /238U in five springs range from 7.2 to 16 in water which has been discharged for at least the past 30,000 years. The anomalies in 234U /238U ratio in deep water have potential usefulness in hydrologic investigations in southern Missouri. Clayey units overlying the spring bog sediments of Trolinger Spring are enriched in 230Th relative to their parent 234U by as much as 720%. The results indicate that both preferential displacement via alpha recoil ejection and the preferential emplacement via recoiling and physical entrapment are significant processes that are occurring in the geologic environment.

  2. Extreme fractionation of 234U 238U and 230Th 234U in spring waters, sediments, and fossils at the Pomme de Terre Valley, southwestern Missouri

    Science.gov (United States)

    Szabo, B. J.

    1982-01-01

    Isotopic fractionation as great as 1600% exists between 234U and 238U in spring waters, sediments, and fossils in the Pomme de Terre Valley, southwestern Missouri. The activity ratios of 234U 238U in five springs range from 7.2 to 16 in water which has been discharged for at least the past 30,000 years. The anomalies in 234U 238U ratio in deep water have potential usefulness in hydrologic investigations in southern Missouri. Clayey units overlying the spring bog sediments of Trolinger Spring are enriched in 230Th relative to their parent 234U by as much as 720%. The results indicate that both preferential displacement via alpha recoil ejection and the preferential emplacement via recoiling and physical entrapment are significant processes that are occurring in the geologic environment. ?? 1982.

  3. The activity concentrations of 40K, 226Ra, 232Th, 238U and 7Be in moss from spas in eastern Serbia in the period 2000-2012

    Directory of Open Access Journals (Sweden)

    Čučulović Ana

    2014-01-01

    Full Text Available In this work we present the activity concentrations of natural radionuclides 40K, 226Ra, 232Th, 238U and 7Be in mosses. One hundred and sixty-seven moss samples were collected between 2001 and 2012 from the territory of the Sokobanja, Banja Jošanica and Gamzigradska Banja spas. They were classified into 23 species. The activity concentrations (Bq/kg in moss from Sokobanja spa were: 40K 25-427; 226Ra 0.3-36; 232Th 1.0-37; 238U 0.4-28 and 7Be 29-210; from Banja Jošanica spa they were: 40K 90-242; 226Ra 2.4-11.7; 232Th 2.0-12.7; 238U 1.6-11.3 and 7Be 142-212; Gamzigradska Banja spa: 40K 95-351; 226Ra 8.0-21; 232Th 5.1-19; 238U 6.7-18 and 7Be 20-144. The activity concentrations of dominant natural radionuclides (potassium, radium, thorium and uranium in the moss samples were within the usual ranges for the territory of Serbia. [Projekat Ministarstva nauke Republike Srbije, br. III 43009

  4. 234U/238U isotope data from groundwater and solid-phase leachate samples near Tuba City Open Dump, Tuba City, Arizona

    Science.gov (United States)

    Johnson, Raymond H.; Horton, Robert J.; Otton, James K.; Ketterer, Michael K.

    2012-01-01

    This report releases 234U/238U isotope data, expressed as activity ratios, and uranium concentration data from analyses completed at Northern Arizona University for groundwater and solid-phase leachate samples that were collected in and around Tuba City Open Dump, Tuba City, Arizona, in 2008.

  5. Transfer of {sup 40}K, {sup 238}U, {sup 210}Pb, and {sup 210}Po from soil to plant in various locations in south of Syria

    Energy Technology Data Exchange (ETDEWEB)

    Al-Masri, M.S. [Atomic Energy Commission of Syria, Damascus, P.O. Box 6091 (Syrian Arab Republic)], E-mail: scientific1@aec.org.sy; Al-Akel, B.; Nashawani, A.; Amin, Y.; Khalifa, K.H.; Al-Ain, F. [Atomic Energy Commission of Syria, Damascus, P.O. Box 6091 (Syrian Arab Republic)

    2008-02-15

    Transfer factors of {sup 40}K, {sup 238}U, {sup 210}Pb, and {sup 210}Po from soil to some agriculture crops in various locations in south of Syria (Dara'a and Assuwaydaa districts) have been determined. Soil and vegetable crops (green pepper, cucumber, tomato, and eggplant), legumes crops (lentil, chickpea, and broad bean), fruit trees (apple, grape, and olives) and cereals (barley and wheat) were collected and analyzed for {sup 238}U, {sup 210}Pb, and {sup 210}Po. The results have shown that higher transfer factors (calculated as Bq kg{sup -1} dry wt. plant material per Bq kg{sup -1} dry wt. soil) for {sup 210}Po, {sup 210}Pb and {sup 238}U were observed in vegetable leaves than fruits and cereals leaves; the highest values of transfer factor (TF) for {sup 238}U were found to be 0.1 for straw of chickpea. Transfer factors for {sup 210}Po varied between 2.8 x 10{sup -2} and 2 in fruits of eggplant and grain of barley, respectively. In addition, several parameters affecting transfer factors of the radionuclides were evaluated. The results can be considered as base values for TF of natural radionuclides in the region.

  6. Axial symmetry around the recoil axis for the 238U(α, α'f) reaction and the fission probability in the giant resonance region

    NARCIS (Netherlands)

    Leo, R. de; Harakeh, M.N.; Micheletti, S.; Plicht, J. van der; van der Woude, Adriaan; David, P.; Janszen, H.

    1982-01-01

    A measurement of the α-spectrum in the region of the isoscalar giant resonances from 238U at Eα = 120 MeV in coincidence with out-of-plane fission fragments shows the validity of the hypothesis of axial symmetry with respect to the recoil axis. Similar to what was observed in previous in-plane

  7. Investigating Uranium Mobility Using Stable Isotope Partitioning of 238U/235U and a Reactive Transport Model

    Science.gov (United States)

    Bizjack, M.; Johnson, T. M.; Druhan, J. L.; Shiel, A. E.

    2015-12-01

    We report a numerical reactive transport model which explicitly incorporates the effectively stable isotopes of uranium (U) and the factors that influence their partitioning in bioactive systems. The model reproduces trends observed in U isotope ratios and concentration measurements from a field experiment, thereby improving interpretations of U isotope ratios as a tracer for U reactive transport. A major factor contributing to U storage and transport is its redox state, which is commonly influenced by the availability of organic carbon to support metal-reducing microbial communities. Both laboratory and field experiments have demonstrated that biogenic reduction of U(VI) fractionates the stable isotope ratio 238U/235U, producing an isotopically heavy solid U(IV) product. It has also been shown that other common reactive transport processes involving U do not fractionate isotopes to a consistently measurable level, which suggests the capacity to quantify the extent of bioreduction occurring in groundwater containing U using 238U/235U ratios. A recent study of a U bioremediation experiment at the Rifle IFRC site (Colorado, USA) applied Rayleigh distillation models to quantify U stable isotope fractionation observed during acetate amendment. The application of these simplified models were fit to the observations only by invoking a "memory-effect," or a constant source of low-concentration, unfractionated U(VI). In order to more accurately interpret the measured U isotope ratios, we present a multi-component reactive transport model using the CrunchTope software. This approach is capable of quantifying the cycling and partitioning of individual U isotopes through a realistic network of transport and reaction pathways including reduction, oxidation, and microbial growth. The model incorporates physical heterogeneity of the aquifer sediments through zones of decreased permeability, which replicate the observed bromide tracer, major ion chemistry, U concentration, and U

  8. Internal tides and sediment dynamics in the deep sea—Evidence from radioactive 234Th/ 238U disequilibria

    Science.gov (United States)

    Turnewitsch, Robert; Reyss, Jean-Louis; Nycander, Jonas; Waniek, Joanna J.; Lampitt, Richard S.

    2008-12-01

    Residual flow, barotropic tides and internal (baroclinic) tides interact in a number of ways with kilometer-scale seafloor topography such as abyssal hills and seamounts. Because of their likely impact on vertical mixing such interactions are potentially important for ocean circulation and the mechanisms and the geometry of these interactions are a matter of ongoing studies. In addition, very little is known about how these interactions are reflected in the sedimentary record. This multi-year study investigates if flow/topography interactions are reflected in distributional patterns of the natural short-lived (half-life: 24.1 d) particulate-matter tracer 234Th relative to its conservative (non-particle-reactive) and very long-lived parent nuclide 238U. The sampling sites were downstream of, or surrounded by, fields of short seamounts and, therefore, very likely to be influenced by nearby flow/topography interactions. At the sampling sites between about 200 and 1000 m above the seafloor recurrent 'fossil' disequilibria were detected. 'Fossil' disequilibria are defined by clearly detectable 234Th/ 238U disequilibria (total 234Th radioactivity current velocities of the predominating tidal M 2 constituent: on (near-)critical seamount slopes baroclinic tides lead to localized [˜ O(1 km)] increases of the overall tidal current velocity by a factor of ˜ 2, thereby pushing the total current velocity well above the threshold for sediment erosion. The results of this and a previous study [Turnewitsch, R., Reyss, J.-L., Chapman, D.C., Thomson, J., Lampitt, R.S., 2004. Evidence for a sedimentary fingerprint of an asymmetric flow field surrounding a short seamount. Earth and Planetary Science Letters 222(3-4), 1023-1036] show that kilometer-scale flow/topography interactions leave a marine geochemical imprint. This imprint may help develop new sediment proxies for the reconstruction of past changes of fluid dynamics in the deep sea, including residual and tidal flow

  9. Spectral interference corrections for the measurement of {sup 238}U in materials rich in thorium by a high resolution {gamma}-ray spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Yuecel, H. [Turkish Atomic Energy Authority (TAEA), Besevler Yerleskesi, Tandogan, 06100 Ankara (Turkey)], E-mail: alfa.haluky@gmail.com; Solmaz, A.N.; Koese, E.; Bor, D. [Institute of Nuclear Sciences of Ankara University (AU-INS), Tandogan, 06100 Ankara (Turkey)

    2009-11-15

    In this study, the spectral interferences are investigated for the analytical peaks at 63.3 keV of {sup 234}Th and 1001.0 keV of {sup 234m}Pa, which are often used in the measurement of {sup 238}U activity by the {gamma}-ray spectrometry. The correction methods are suggested to estimate the net peak areas of the {gamma}-rays overlapping the analytical peaks, due to the contribution of {sup 232}Th that may not be negligible in materials rich in natural thorium. The activity results for the certified reference materials (CRMs) containing U and Th were measured with a well type Ge detector. The self-absorption and true coincidence-summing (TCS) effects were also taken into account in the measurements. It is found that ignoring the contributions of the interference {gamma}-rays of {sup 232}Th and {sup 235}U to the mixed peak at 63.3 keV of {sup 234}Th ({sup 238}U) leads to the remarkably large systematic influence of 0.8-122% in the measured {sup 238}U activity, but in case of ignoring the contribution of {sup 232}Th via the interference {gamma}-ray at 1000.7 keV of {sup 228}Ac to the mixed peak at 1001 keV of {sup 234m}Pa ({sup 238}U) results in relatively smaller systematic influence of 0.05-3%, depending on thorium contents in the samples. The present results showed that the necessary correction for the spectral interferences besides self-absorption and TCS effects is also very important to obtain more accurate {sup 238}U activity results. Additionally, if one ignores the contribution of {sup 232}Th to both {sup 238}U and {sup 40}K activities in materials, the maximum systematic influence on the effective radiation dose is estimated to be {approx}6% and {approx}1% via the analytical peaks at 63.3 and 1001 keV for measurement of the {sup 238}U activity, respectively.

  10. Determination of extremely low (236)U/(238)U isotope ratios in environmental samples by sector-field inductively coupled plasma mass spectrometry using high-efficiency sample introduction.

    Science.gov (United States)

    Boulyga, Sergei F; Heumann, Klaus G

    2006-01-01

    A method by inductively coupled plasma mass spectrometry (ICP-MS) was developed which allows the measurement of (236)U at concentration ranges down to 3 x 10(-14)g g(-1) and extremely low (236)U/(238)U isotope ratios in soil samples of 10(-7). By using the high-efficiency solution introduction system APEX in connection with a sector-field ICP-MS a sensitivity of more than 5,000 counts fg(-1) uranium was achieved. The use of an aerosol desolvating unit reduced the formation rate of uranium hydride ions UH(+)/U(+) down to a level of 10(-6). An abundance sensitivity of 3 x 10(-7) was observed for (236)U/(238)U isotope ratio measurements at mass resolution 4000. The detection limit for (236)U and the lowest detectable (236)U/(238)U isotope ratio were improved by more than two orders of magnitude compared with corresponding values by alpha spectrometry. Determination of uranium in soil samples collected in the vicinity of Chernobyl nuclear power plant (NPP) resulted in that the (236)U/(238)U isotope ratio is a much more sensitive and accurate marker for environmental contamination by spent uranium in comparison to the (235)U/(238)U isotope ratio. The ICP-MS technique allowed for the first time detection of irradiated uranium in soil samples even at distances more than 200 km to the north of Chernobyl NPP (Mogilev region). The concentration of (236)U in the upper 0-10 cm soil layers varied from 2 x 10(-9)g g(-1) within radioactive spots close to the Chernobyl NPP to 3 x 10(-13)g g(-1) on a sampling site located by >200 km from Chernobyl.

  11. Gamma-Ray Emission Spectra as a Constraint on Calculations of 234 , 236 , 238U Neutron-Capture Cross Sections

    Science.gov (United States)

    Ullmann, J. L.; Krticka, M.; Kawano, T.; Bredeweg, T. A.; Baramsai, B.; Couture, A.; Haight, R. C.; Jandel, M.; Mosby, S.; O'Donnell, J. M.; Rundberg, R. S.; Vieira, D. J.; Wilhelmy, J. B.; Becker, J. A.; Wu, C. Y.; Chyzh, A.

    2015-10-01

    Calculations of the neutron-capture cross section at low neutron energies (10 eV through 100's of keV) are very sensitive to the nuclear level density and radiative strength function. These quantities are often poorly known, especially for radioactive targets, and actual measurements of the capture cross section are usually required. An additional constraint on the calculation of the capture cross section is provided by measurements of the cascade gamma spectrum following neutron capture. Recent measurements of 234 , 236 , 238U(n, γ) emission spectra made using the DANCE 4 π BaF2 array at the Los Alamos Neutron Science Center will be presented. Calculations of gamma-ray spectra made using the DICEBOX code and of the capture cross section made using the CoH3 code will also be presented. These techniques may be also useful for calculations of more unstable nuclides. This work was performed with the support of the U.S. Department of Energy, National Nuclear Security Administration by Los Alamos National Security, LLC (Contract DE-AC52-06NA25396) and Lawrence Livermore National Security, LLC (Contract DE-AC52-07NA2734).

  12. Neutron capture cross section measurements of $^{238}$U, $^{241}$Am and $^{243}$Am at n_TOF

    CERN Multimedia

    Koehler, P E; Plag, R

    The increase of the world energy demand and the need of low carbon energy sources have triggered the renaissance and/or enhancement of nuclear energy in many countries. Fundamental nuclear physics can contribute in a practical way to the sustainability and safety of the nuclear energy production and the management of the nuclear waste. There exists a series of recent studies which address the most relevant isotopes, decay data, nuclear reaction channels and energy ranges which have to be investigated in more detail for improving the design of different advanced nuclear systems [1] and nuclear fuel cycles [2]. In this proposal, we aim at the measurement of the neutron capture cross sections of $^{238}$U, $^{241}$Am and $^{243}$Am. All three isotopes are listed in the NEA High Priority Request List [37], are recommended for measurements [1] and play an important role in the nuclear energy production and fuel cycle scenarios. The measurements will provide as well valuable nuclear structure data necessary for the...

  13. Fission-fragment properties in 238U(n ,f ) between 1 and 30 MeV

    Science.gov (United States)

    Duke, D. L.; Tovesson, F.; Laptev, A. B.; Mosby, S.; Hambsch, F.-J.; Bryś, T.; Vidali, M.

    2016-11-01

    The fragment mass and kinetic energy in neutron-induced fission of 238U has been measured for incident energies from 1 to 30 MeV at the Los Alamos Neutron Science Center. The change in mass distributions over this energy range were studied, and the transition from highly asymmetric to more symmetric mass distributions is observed. A decrease in average total kinetic energy (TKE ¯) with increasing excitation energy is observed, consistent with previous experimental work. Additional structure at multichance fission thresholds is present in the TKE ¯ data. The correlations between fragment masses and total kinetic energy and how that changes with excitation energy of the fissioning compound nucleus were also measured. The fission mass yields and average total kinetic energy are important for fission-based technologies such as nuclear reactors to understand nuclear waste generation and energy output when developing new and advanced concepts. The correlations between fragment mass and kinetic energy are needed both as input for theoretical calculations of the deexcitation process in fission fragments by prompt radiation emission and for validating advanced theoretical fission models describing the formation of the primordial fragments.

  14. Photo-fission Product Yield Measurements at Eγ=13 MeV on 235U, 238U, and 239Pu

    Science.gov (United States)

    Tornow, W.; Bhike, M.; Finch, S. W.; Krishichayan, Fnu; Tonchev, A. P.

    2016-09-01

    We have measured Fission Product Yields (FPYs) in photo-fission of 235U, 238U, and 239Pu at TUNL's High-Intensity Gamma-ray Source (HI γS) using mono-energetic photons of Eγ = 13 MeV. Details of the experimental setup and analysis procedures will be discussed. Yields for approximately 20 fission products were determined. They are compared to neutron-induced FPYs of the same actinides at the equivalent excitation energies of the compound nuclear systems. In the future photo-fission data will be taken at Eγ = 8 . 0 and 10.5 MeV to find out whether photo-fission exhibits the same so far unexplained dependence of certain FPYs on the energy of the incident probe, as recently observed in neutron-induced fission, for example, for the important fission product 147Nd. Work supported by the U. S. Dept. of Energy, under Grant No. DE-FG02-97ER41033, and by the NNSA, Stewardship Science Academic Alliances Program, Grant No. DE-NA0001838 and the Lawrence Livermore, National Security, LLC under Contract No. DE-AC52-07NA27344.

  15. Behaviour of {sup 238}U, {sup 234}U, {sup 228}Ra and {sup 226}Ra in rock alterations: study of Morungaba granitoids, SP-Brazil and ground water in its fractures; Comportamento de {sup 238}U, {sup 234}U, {sup 228}Ra e {sup 226}Ra na alteracao de rochas: estudo dos granitoides de Morungaba (SP) e aguas subterraneas de suas fraturas

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Rosana N. dos [Pontificia Univ. Catolica de Sao Paulo, SP (Brazil). Dept. de Fisica]. E-mail: rosana@pucsp.br; Marques, Leila S. [Sao Paulo Univ., SP (Brazil). Inst. de Astronomia, Geofisica e Ciencias Atmosfericas. Dept. de Geofisica]. E-mail: leila@iag.usp.br

    2005-07-01

    This work presents the first results obtained on the investigation of the behavior of uranium and radium radioisotopes in the processes of weathering and rock-water interaction of Morungaba granitoids belonging to Meridional Pluton (Valinhos Town-SP-Brazil). Specific activities of {sup 238}U, {sup 234}U, {sup 228}Ra and {sup 226}Ra were determined in non altered granitoids (Group A), as well as in those affected by different degrees of weathering (Groups B, C and D). The uranium specific activities were determined by alpha spectrometry method, whereas for the determination of radium isotopes high resolution gamma-ray spectrometry technique was employed. The data indicate that {sup 238}U and {sup 234}U are in radioactive equilibrium in the fresh analyzed granitoids, but show a slight depletion of {sup 234}U in relation to {sup 238}U in the weathered rocks. The ({sup 226}Ra/{sup 238}U) and ({sup 226}Ra/{sup 234}U) activity ratios of all investigated rocks are similar, showing a significant {sup 226}Ra depletion, which is probably caused by its preferential leaching. These results indicate that even samples macroscopically classified as fresh rocks, their systems have been opened for some geochemical changes. The high ({sup 234}U/{sup 238}U) activity ratios of groundwaters which are found in the fractures of these granitoids suggest their prolonged residence times in the aquifer and/or their percolation by other rocks presenting different geochemical properties. (author)

  16. Activity ratios of (234)U/(238)U and (226)Ra/(228)Ra for transport mechanisms of elevated uranium in alluvial aquifers of groundwater in south-western (SW) Punjab, India.

    Science.gov (United States)

    Kumar, A; Karpe, R K; Rout, S; Gautam, Y P; Mishra, M K; Ravi, P M; Tripathi, R M

    2016-01-01

    The concentrations of total dissolved uranium (U), its isotopic composition ((234)U, (235)U, (238)U) and two long lived Ra isotopes ((226)Ra and (228)Ra) in alluvial aquifers of groundwater were determined to investigate the groundwater flow pattern in the south-western (SW) Punjab, India. Particular attention was given to the spatial variability of activity ratios (ARs) of (234)U/(238)U and (226)Ra/(228)Ra to predict the possible sources and supply process of U into the water from the solid phase. The measured groundwater (234)U/(238)U ARs were ∼1 or >1 in the shallow zone (depth  30 m) with relatively low U concentration. The simultaneous elevated U concentration and (234)U/(238)U ARs in waters were possibly due to differences in imprints of rock-water interactions under hydrologic conditions. However, (234)U/(238)U ARs aquifers.

  17. Activity concentrations of {sup 238}U and {sup 226}Ra in scales formed on pipes of industrial boilers in the state of Pernambuco, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Poggi, Claudia M.B.; Farias, Emerson E.G. de, E-mail: claudiapoggi04@gmail.com, E-mail: emersonemiliano@yahoo.com.br [Universidade Federal de Pernambuco (UFPE), Recife, PE (Brazil). Departamento de Energia Nuclear; Franca, Elvis J.; Hazin, Clovis A., E-mail: chazin@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil); Gazineu, Maria H.P., E-mail: helena@unicap.br [Universidade Catolica de Pernambuco (UNICAP), Recife, PE (Brazil). Centro de Ciencias e Tecnologia

    2015-07-01

    The procedures employed in the industry can generate significant amounts of solid, liquid and gaseous wastes that usually contain toxic or materials of difficulty degradation. One of the facts that contribute to the formation of such wastes is the generation of steam used in operating processes and industry segments. Currently, steam supplied by boilers is the most economical and practical mode of heat transfer in industrial processes. Due to the high temperature of water used in these processes, compounds which were previously soluble become insoluble, generating residues called scales. This material, which contains stable ions, can also present naturally occurring radionuclides such as {sup 238}U and {sup 226}Ra, which concentrate over time in piping and equipment surfaces. If not disposed correctly, this material also can contaminate the environment. The main origin of these radionuclides is the use of groundwater in industrial processes. Thus, in regions of naturally enriched in radionuclides such as the Region of Pernambuco, including the municipalities of Paulista and Goiana, there is a greater possibility of radioactive scale formation. Therefore, this study aimed to determine the activity concentrations of {sup 238}U and {sup 226}Ra present in the solid wastes generated by industries situated in Paulista and Goiana, in order to assess radionuclide disequilibrium. For the sake of comparison, scale samples collected from industries located in the municipality of Caruaru, far from the previous municipalities, were also analyzed. The determination of the activity concentrations for {sup 238}U and {sup 226}Ra was performed by High Resolution Gamma-Ray Spectrometry. Samples were collected, prepared, packed in plastic containers and set aside for a minimum time of 21 days, for the secular equilibrium to occur between {sup 226}Ra and its short lived descendants. The counting time was 80,000 seconds. Gamma energies used for determination of activity concentrations

  18. Bioaccumulation of polonium ({sup 210}Po) and uranium ({sup 234}U, {sup 238}U) in plants around phosphogypsum waste heap in Wislinka (northern Poland)

    Energy Technology Data Exchange (ETDEWEB)

    Borylo, A.; Skwarzec, B. [Gdansk Univ. (Poland). Faculty of Chemistry

    2011-07-01

    In the study the activities of polonium {sup 210}Po and uranium {sup 234}U, {sup 238}U in plants, collected near phosphogypsum waste heap in Wis'linka (northern Poland), were determined by using the alpha spectrometry. The obtained results revealed that the concentrations of {sup 210}Po, {sup 234}U, and {sup 238}U in the analyzed plants were differentiated. In the analyzed flora organisms the highest amounts of polonium and uranium were found in ruderal plant samples as well as willow samples (Salix viminalis) from protection zone of phosphogypsum waste heap. The concentrations of {sup 210}Po, {sup 234}U and {sup 238}U in the analyzed plants were higher in roots than in green parts of plants. The higher concentrations of {sup 210}Po and {sup 238}U radionuclides were estimated for hydrophyte (common sedge Carex nigra Reichard), the favourite habitat of which is particularly wet meadow and for plants collected in the vicinity of phosphogypsum waste heap. The major source of polonium and uranium in analyzed plants is root system. The values of {sup 234}U/ {sup 238}U activity ratio in all analyzed plants are closed to one, what indicated that source of uranium in analyzed plants is phosphogypsum. The highest uranium and polonium concentrations were characterized for plants, which are covered with tomentose. The comparability polonium and uranium contents were confirmed in edible plants, but higher accumulation was determined in ripe species than immature species of vegetables. The higher polonium and uranium concentrations were noticed in green parts of plant, the lower in roots. Polonium concentration in cultivated plants samples was not species diverse. Therefore, the significant source of polonium and uranium in analyzed plants is wet and dry atmospheric falls gathering the soil and air dust from phosphogypsum waste dump. The maximum {sup 210}Po and {sup 238}U radionuclides concentrations were found in green parts of red beet (Beta vulgaris esculenta), the

  19. Bioaccumulation of polonium (210Po, uranium (234U, 238U isotopes and trace metals in mosses from Sobieszewo Island, northern Poland

    Directory of Open Access Journals (Sweden)

    Boryło A.

    2013-04-01

    Full Text Available The objective of this study was determination of the polonium (210Po, uranium (234U and 238U radionuclides and trace metals (Pb, Fe, Zn, Cu, Ni, Cd, Hg concentrations in mosses samples from Sobieszewo Island near the phosphogypsum waste dump in Wiślinka (northern Poland. The obtained results revealed that the concentrations of 210Po, 234U, and 238U in the two analyzed kinds of mosses: Pleurozium schreberi and Dicranum scoparium were similar. Among the analyzed trace metals the highest concentration in mosses was recorded for iron, while the lowest for nickel, cadmium and mercury. The obtained studies showed that the sources of polonium and uranium isotopes, as well as trace metals in analyzed mosses are air city contaminations transported from Gdańsk and from existing in the vicinity the phosphogypsum waste heap in Wiślinka (near Gdańsk.

  20. Low-energy fission investigated in reactions of 750 AMeV {sup 238}U-ions with Pb and Be targets. Pt. 1. Nuclear charge distributions

    Energy Technology Data Exchange (ETDEWEB)

    Armbruster, P. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Bernas, M. [IPN Orsay, 91 Orsay (France); Czajkowski, S. [IPN Orsay, 91 Orsay (France); Geissel, H. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Aumann, T. [Mainz Univ. (Germany). Inst. fuer Kernchemie; Dessagne, P. [Strasbourg-1 Univ., 67 (France). Centre de Recherches Nucleaires; Donzaud, C. [IPN Orsay, 91 Orsay (France); Hanelt, E. [Technische Hochschule Darmstadt (Germany). Inst. fuer Kernphysik; Heinz, A. [Technische Hochschule Darmstadt (Germany). Inst. fuer Kernphysik; Hesse, M. [Tuebingen Univ. (Germany). Physikalisches Inst.; Kozhuharov, C. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Miehe, C. [Strasbourg-1 Univ., 67 (France). Centre de Recherches Nucleaires; Muenzenberg, G. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Pfuetzner, M. [Warsaw Univ. (Poland); Schmidt, K.H. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Schwab, W. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Stephan, C. [IPN Orsay, 91 Orsay (France); Suemmerer, K. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Tassan-got, L. [IPN Orsay, 91 Orsay (France); Voss, B. [Technische Hochschule Darmstadt (Germany). Inst. fuer Kernphysik

    1996-07-01

    Charge distributions of fragments from low energy nuclear fission are investigated in reactions of highly fissile {sup 238}U projectiles at relativistic energies (750 A.MeV) with a heavy (Pb) and a light (Be) target. The fully stripped fission fragments are separated by the fragment separator (FRS). Their high kinetic energies in the laboratory system allow the identification of all atomic numbers by using multiple-sampling ionization chambers (MUSIC). The elemental distributions of fragments observed at larger magnetic rigidities than the {sup 238}U projectiles show asymmetric break-up and odd-even effects. They indicate a low energy fission process, induced mainly by dissociation in the electro-magnetic field for the U/Pb-system, or by peripheral nuclear interactions for the U/Be-system. (orig.)

  1. Low energy fission investigated in reactions of 750 AMeV {sup 238}U-ions with Pb and Be targets

    Energy Technology Data Exchange (ETDEWEB)

    Armbruster, P. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Bernas, M. [Paris-11 Univ., 91 - Orsay (France). Inst. de Physique Nucleaire; Czajkowski, S. [Paris-11 Univ., 91 - Orsay (France). Inst. de Physique Nucleaire; Geissel, H. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Aumann, T. [Mainz Univ. (Germany). Inst. fuer Kernchemie; Dessagne, P. [Strasbourg-1 Univ., 67 (France). Centre de Recherches Nucleaires; Donzaud, C. [Paris-11 Univ., 91 - Orsay (France). Inst. de Physique Nucleaire; Hanelt, E. [Technische Hochschule Darmstadt (Germany). Inst. fuer Kernphysik; Heinz, A. [Technische Hochschule Darmstadt (Germany). Inst. fuer Kernphysik; Hesse, M. [Tuebingen Univ. (Germany). Physikalisches Inst.; Kozhuharov, C. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Miehe, C. [Strasbourg-1 Univ., 67 (France). Centre de Recherches Nucleaires; Muenzenberg, G. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Pfuetzner, M. [Warsaw Univ. (Poland); Schmidt, K.H. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Schwab, W. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Stephan, C. [Paris-11 Univ., 91 - Orsay (France). Inst. de Physique Nucleaire; Suemmerer, K. [Gesellschaft fuer Schwerionenforschung mbH, Darmstadt (Germany); Tassan-Got, L. [Paris-11 Univ., 91 - Orsay (France). Inst. de Physique Nucleaire; Voss, B. [Technische Hochschule Darmstadt (Germany). Inst. fuer Kernphysik

    1995-10-01

    Charge distributions of fragments from low energy nuclear fission are investigated in reactions of highly fissile {sup 238}U projectiles at relativistic energies (750 AMeV) with a heavy (Pb) and a light (Be) target. The fully stripped fission fragments are separated by the Fragment Separator (FRS). Their high kinetic energies in the laboratory system allow the identification of all atomic numbers by using Multiple-Sample Ionization Chambers (MUSIC). The elemental distributions of fragments observed at larger magnetic rigidities than the {sup 238}U projectiles show asymmetric break-up and odd-even effects. They indicate a low energy fission process, induced mainly by dissociation in the electromagnetic field for the U/Pb-system, or by peripheral nuclear interactions for the U/Be-system. (orig.)

  2. Low-energy fission investigated in reactions of 750 AMeV238U-ions with Pb and Be targets. I. Nuclear charge distributions

    Science.gov (United States)

    Armbruster, P.; Bernas, M.; Czajkowski, S.; Geissel, H.; Aumann, T.; Dessagne, Ph.; Donzaud, C.; Hanelt, E.; Heinz, A.; Hesse, M.; Kozhuharov, C.; Miehe, Ch.; Münzenberg, G.; Pfützner, M.; Schmidt, K.-H.; Schwab, W.; Stéphan, C.; Sümmerer, K.; Tassan-Got, L.; Voss, B.

    1996-12-01

    Charge distributions of fragments from low energy nuclear fission are investigated in reactions of highly fissile238U projectiles at relativistic energies (750 A·MeV) with a heavy (Pb) and a light (Be) target. The fully stripped fission fragments are separated by the Fragment Separator (FRS). Their high kinetic energies in the laboratory system allow the identification of all atomic numbers by using Multiple-Sampling Ionization Chambers (MUSIC). The elemental distributions of fragments observed at larger magnetic rigidities than the238U projectiles show asymmetric break-up and odd-even effects. They indicate a low energy fission process, induced mainly by dissociation in the electro-magnetic field for the U/Pb-system, or by peripheral nuclear interactions for the U/Be-system.

  3. Towards the high-accuracy determination of the 238U fission cross section at the threshold region at CERN – n_TOF

    Directory of Open Access Journals (Sweden)

    Diakaki M.

    2016-01-01

    Full Text Available The 238U fission cross section is an international standard beyond 2 MeV where the fission plateau starts. However, due to its importance in fission reactors, this cross-section should be very accurately known also in the threshold region below 2 MeV. The 238U fission cross section has been measured relative to the 235U fission cross section at CERN – n_TOF with different detection systems. These datasets have been collected and suitably combined to increase the counting statistics in the threshold region from about 300 keV up to 3 MeV. The results are compared with other experimental data, evaluated libraries, and the IAEA standards.

  4. A beta-alpha coincidence counting system for measurement of trace quantities of 238U and 232Th in aqueous samples at the Sudbury Neutrino Observatory.

    Science.gov (United States)

    Dawson, M.; Doucas, G.; Fergani, H.; Jelley, N. A.; Majerus, S.; O'Keeffe, H. M.; Peeters, S. J. M.; Perry, C.

    2016-08-01

    The Sudbury Neutrino Observatory experiment was built to measure the total flux of 8B solar neutrinos via the neutral current disintegration deuterium nuclei. This process can be mimiced by daughter isotopes of 232Th and 238U which can photodisintegrate the deuterium nucleus. Measurement of the concentration of such radioisotopes in the heavy water was critical to the success of the experiment. A radium assay technique using Hydrous Titanium Oxide coated filters was developed for this purpose and it was used in conjunction with a delayed beta-alpha coincidence counting system. The design, calibration and operation of this counting system are described in this paper. The counting efficiency for 232Th (224Ra) and 238U (226Ra) were measured to be 50 ± 5% and 62 ± 7%

  5. Study of the 238U(d,p) surrogate reaction via the simultaneous measurement of gamma-decay and fission probabilities

    CERN Document Server

    Ducasse, Q; Aïche, M; Marini, P; Mathieu, L; Görgen, A; Guttormsen, M; Larsen, A C; Tornyi, T; Wilson, J N; Barreau, G; Boutoux, G; Czajkowski, S; Giacoppo, F; Gunsing, F; Hagen, T W; Lebois, M; Lei, J; Méot, V; Morillon, B; Moro, A; Renstrøm, T; Roig, O; Rose, S J; Sérot, O; Siem, S; Tsekhanovich, I; Tveten, G M; Wiedeking, M

    2015-01-01

    We investigated the 238U(d,p) reaction as a surrogate for the n + 238U reaction. For this purpose we measured for the first time the gamma-decay and fission probabilities of 239U* simultaneously and compared them to the corresponding neutron-induced data. We present the details of the procedure to infer the decay probabilities, as well as a thorough uncertainty analysis, including parameter correlations. Calculations based on the continuum-discretized coupled-channels and distorted-wave Born approximations were used to correct our data from detected protons originating from elastic and inelastic deuteron breakup. The corrected fission probability is in agreement with neutron-induced data, whereas the gamma-decay probability is much higher than the neutron-induced data. The performed statistical-model calculations are not able to explain these results.

  6. Determination of {sup 234}U/{sup 238}U isotope ratios in environmental waters by quadrupole ICP-MS after U stripping from alpha-spectrometry counting sources

    Energy Technology Data Exchange (ETDEWEB)

    Mas, Jose L.; Gonzalez-Labajo, Jesus [Universidad de Sevilla, Escuela Universitaria Politecnica, Departamento de Fisica Aplicada I, Sevilla (Spain); Ma, Renli [Northumbria University, School of Applied Sciences, Newcastle upon Tyne (United Kingdom); McLeod, Cameron; Cox, Alan [University of Sheffield, Department of Analytical Chemistry, Sheffield (United Kingdom); Watson, Paul [Elemental Scientific, Inc., Omaha, NE 68131 (United States)

    2006-09-15

    The {sup 234}U/{sup 238}U isotope ratio has been widely used as a tracer for geochemical processes in underground aquifers. Quadrupole-based inductively coupled plasma mass spectrometry (ICP-MS) equipped with a high-efficiency nebulizer and a membrane desolvator was employed for the determination of {sup 234}U/{sup 238}U isotope ratios in natural water samples. The instrumental limit of detection for {sup 234}U was at the low pg L{sup -1} level with very low sample consumption. Measurement precision ({sup 234}U/{sup 238}U) was 3-5% for bottled mineral water with elevated uranium concentration (>1 {mu}g L{sup -1}). For the analysis of groundwater samples from the Almonte-Marisma underground aquifer (Huelva, Spain), uranium was stripped from stainless steel planchets that had previously been used as radiometric counting sources for alpha-particle spectrometry. Potential spectral interferences from other metals introduced during the dissolution were investigated. Matrix-matched blank solutions were needed to subtract the background on {sup 234}U due to the formation of platinum argides, and to allow for mass bias correction and background correction. The Pt appears to be an impurity present in the stainless steel, either as a minor component by itself or after extraction from the anode and a subsequent uranium electrodeposition. The {sup 234}U/{sup 238}U isotope ratio data were in very good agreement with those of alpha spectrometry, while precision was improved by a factor of up to 10 and counting time was reduced down to {proportional_to}20 min (10 replicate measurements). (orig.)

  7. Influence of soil texture on the distribution and availability of {sup 238}U, {sup 230}Th, and {sup 226}Ra in soils

    Energy Technology Data Exchange (ETDEWEB)

    Blanco Rodriguez, P. [Departamento de Fisica, Facultad de Ciencias, Universidad de Extremadura, Avd. Elvas s/n, 06071 Badajoz (Spain); Vera Tome, F. [Departamento de Fisica Aplicada, Facultad de Ciencias, Universidad de Extremadura, Avd. Elvas s/n, 06071 Badajoz (Spain)], E-mail: fvt@unex.es; Lozano, J.C. [Laboratorio de Radiactividad Ambiental, Facultad de Ciencias, Universidad de Salamanca, 37008 Salamanca (Spain); Perez-Fernandez, M.A. [Area de Ecologia, Universidad Pablo Olavide, Carretera de Utrera km. 1, 41013 Sevilla (Spain)

    2008-08-15

    The influence of soil texture on the distribution and availability of {sup 238}U, {sup 230}Th, and {sup 226}Ra in soils was studied in soil samples collected at a rehabilitated uranium mine located in the Extremadura region in south-west Spain. The activity concentration (Bq kg{sup -1}) in the soils ranged from 60 to 750 for {sup 238}U, from 60 to 260 for {sup 230}Th, and from 70 to 330 for {sup 226}Ra. The radionuclide distribution was determined in three soil fractions: coarse sand (0.5-2 mm), medium-fine sand (0.067-0.5 mm), and silt and clay (<0.067 mm). The relative mobility of the natural radionuclides in the different fractions was studied by comparison of the activity ratios between radionuclides belonging to the same radioactive series. The lability of these radionuclides in each fraction was also studied through selective extraction from the soils using a one-step sequential extraction scheme. Significant correlations were found for {sup 238}U, {sup 230}Th, and {sup 226}Ra between the activity concentration per fraction and the total activity concentration in the bulk soil. Thus, from the determination of the activity concentration in the bulk soil, one could estimate the activity concentration in each fraction. Correlations were also found for {sup 238}U and {sup 226}Ra between the labile activity concentration in each fraction and the total activity concentration in bulk soil. Assuming that there is some particle-size fraction that predominates in the process of soil-to-plant transfer, the parameters obtained in this study should be used as correction factors for the transfer factors determined from the bulk soil in previous studies.

  8. Non-destructive field measurement of the ratio /sup 235/U//sup 238/U in depleted to moderately enriched uranium

    Energy Technology Data Exchange (ETDEWEB)

    Balagna, J.P.; Cowan, G.A.

    1977-01-01

    The exploration of a natural reactor site is expedited by prompt measurement of /sup 235/U to /sup 238/U ratios near the mining operation. An instrument has been constructed which uses the relative fission rates of /sup 235/U and /sup 238/U in fast and moderated neutron spectra to measure the isotopic ratio. This device can be placed in the field and allows continuous monitoring of ore as a rich deposit of uranium is mined. With rapid return of isotopic information to the operator it is possible to locate a fossil reactor before it has been destroyed. The relative fast neutron and slow neutron fission rates induced in uranium which is depleted to moderately enriched in /sup 235/U may be used to measure the isotopic ratio /sup 235/U//sup 238/U quickly and nondestructively with a relative error of a few percent. When a neutron source such as /sup 252/Cf is used, the measurements may be made in the field.

  9. Charge-state distribution measurements of ^{238}U and ^{136}Xe at 11  MeV/nucleon using gas charge stripper

    Directory of Open Access Journals (Sweden)

    H. Kuboki

    2010-09-01

    Full Text Available The charge-state distributions and equilibrium charge states of uranium (^{238}U and xenon (^{136}Xe ions at 11  MeV/nucleon were determined using a gas charge stripper. A differential pumping system facilitated the increase of the nitrogen gas thickness up to 1.3  mg/cm^{2}, which is sufficient for the most probable charge state to attain equilibrium. The charge states of ^{238}U attain equilibrium at 56.0, 56.6, and 55.7 in N_{2}, Ar, and CO_{2} media with thicknesses of 125, 79, and 126  μg/cm^{2}, respectively, while those of ^{136}Xe attain equilibrium at 40.5, 40.1, and 40.3 in N_{2}, Ar, and CO_{2} media with thicknesses of 163, 95, and 139  μg/cm^{2}, respectively. The equilibrium charge states of ^{136}Xe are acceptable for acceleration by the subsequent cyclotron. The measured data of ^{238}U were used to devise an empirical formula for the prediction of the equilibrium charge state in gaseous media over the energy region of 0.01–60  MeV/nucleon. The equilibrium charge state of ^{136}Xe as predicted by the devised formula is in good agreement with the data.

  10. Uranium ((234)U, (235)U and (238)U) contamination of the environment surrounding phosphogypsum waste heap in Wiślinka (northern Poland).

    Science.gov (United States)

    Olszewski, Grzegorz; Boryło, Alicja; Skwarzec, Bogdan

    2015-08-01

    The aim of this work was to determine the uranium concentration ((234)U, (235)U and (238)U) and values of the activity ratio (234)U/(238)U in soil samples collected near phosphogypsum waste heap in Wiślinka (northern Poland). On the basis of the studies it was found that the values of the (234)U/(238)U activity ratio in the analyzed soils collected in the vicinity of phosphogypsum dump in Wiślinka are in most cases close to one and indicate the phosphogypsum origin of the analyzed nuclides. The obtained results of uranium concentrations are however much lower than in previous years before closing of the phosphogypsum stockpile. After this process and covering the phosphogypsum stockpile in Wiślinka with sewage sludge, phosphogypsum particles are successfully immobilized. In the light of the results the use of phosphate fertilizers seems to be a major problem. Prolonged and heavy rains can cause leaching accumulated uranium isotopes in the phosphogypsum stockpile, which will be washed into the Martwa Wisła and on the fields in the immediate vicinity of this storage.

  11. Equilibrium and Disequilibrium of 230Th-238U in Zircon from the Minoan Eruption, Santorini, Aegean Sea, Greece

    Science.gov (United States)

    Schmitt, A. K.; Stockli, D. F.; Song, E. J.; Storm, S.

    2016-12-01

    The Minoan eruption (ca. 1600 BCE; 40-80 km3 dense rock equivalent) occurred after a ca. 18 ka period of dormancy followed by rapid reinvigoration through arrival of new magma from deep reservoirs colliding with evolved magmas in shallow storage. Although zoned phenocrysts indicate brief timescales ranging between years to decades for final pre-eruptive magma recharge and mixing, it remains unclear how magma accumulation vs. crystallization were balanced in the subvolcanic reservoir during the preceding inter-eruptive cycle. To directly probe magma presence over the repose interval prior to the Minoan eruption and further back in time, we reconnoitered the potential of U-Th zircon geochronology to date the crystallization of individual zircon crystals from pumice from the Minoan eruption. Zircon crystals were extracted from composite pumice samples (several kg each) from basal fall out deposits using gravity and magnetic separation. Etching in cold HF removed adherent glass and revealed the shape of crystals, which were pressed into indium metal to expose unpolished rims to the ion beam of a CAMECA IMS 1270 secondary ionization mass spectrometer. Adherent glass was ubiquitous, indicating that crystals were in contact with melt at the time of eruption. Six of 18 crystals were in 230Th/238U secular equilibrium, two crystals yielded ages of ca. 160 ka, and the remaining rims dated between eruption age and ca. 20 ka. Low Th/U of some secular equilibrium zircon suggests recycling of metamorphic basement zircon, which is also indicated by the presence of rutile in heavy mineral separates. U-Th dates also reveal recycling of zircon from Pleistocene intrusions that likely represent left-over magma from antecedent eruption cycles. We tentatively interpret the dominant zircon population with near-eruption to ca. 20 ka ages to indicate continuous melt presence underneath Santorini during the last repose interval. Distinguishing a hiatus in zircon crystallization between 20 ka

  12. The metrological activity determination of {sup 238} U and {sup 230} Th by gamma spectrometry to industrial fuel-cycle application

    Energy Technology Data Exchange (ETDEWEB)

    Almeida M, M.C. de; Delgado, J.U.; Poledna, R. [Instituto de Radioprotecao e Dosimetria- IRD/SEMRA, CNEN, Av. Salvador Allende s/n, Recreio, CEP 22780-160, Rio de Janeiro (Brazil)]. e-mail: marcandida@yahoo.com.br

    2006-07-01

    This work describes the difficulty for determining the activity of {sup 238} U and {sup 230} Th using gamma spectrometry due to the low gamma-ray emission probabilities of 92 and 67 keV, and, mainly, the associated high uncertainties about 13 and 11%, respectively. {sup 230} Th is a {sup 238} U daughter and it is product from uranium mills and refineries. {sup 230} Th decays to {sup 226} Ra and this decay has to be measured because these radionuclides are not in secular equilibrium with their daughter products, besides the gamma-energies have high uncertainties in the emission probabilities. These radionuclides, mostly {sup 238} U, are important in the nuclear fuel-cycle, since the mining of uranium ore, where the nominal isotopic content of natural uranium is 99.27% of {sup 238} U, until the irradiated fuel reprocessing, where this isotope, a fertile material, is recovered to be used again. The uranium and thorium are considered safeguarded nuclear materials and the metrology tries to calibrate and standardize these materials to improve the activity determination techniques applied in different fuel-cycle scopes. The essential characteristics of the safeguarded materials are low gamma energies (less than 100 keV) and emission probabilities but with high uncertainties. In this way, the metrology can contribute to homeland security defense against illicit nuclear trafficking with the identification and quantification of the safeguarded radionuclides such as uranium and thorium, using specific gamma window energy and high resolution planar or coaxial germanium detector. The efficiency curve is obtained from the reference source spectrum considering the photopeak areas corresponding the standard activities. This curve depends on radiation energy, sample geometry, photon attenuation (sample absorption and material absorption between sample-detector), dead time and sample-detector position. The metrological activity determinations of {sup 238} U solid sources, and of

  13. 238U series isotopes and 232Th in carbonates and black shales from the Lesser Himalaya: implications to dissolved uranium abundances in Ganga-Indus source waters.

    Science.gov (United States)

    Singh, S K; Dalai, Tarun K; Krishnaswami, S

    2003-01-01

    238U and (232)Th concentrations and the extent of (238)U-(234)U-(230)Th radioactive equilibrium have been measured in a suite of Precambrian carbonates and black shales from the Lesser Himalaya. These measurements were made to determine their abundances in these deposits, their contributions to dissolved uranium budget of the headwaters of the Ganga and the Indus in the Himalaya and to assess the impact of weathering on (238)U-(234)U-(230)Th radioactive equilibrium in them. (238)U concentrations in Precambrian carbonates range from 0.06 to 2.07 microg g(-1). The 'mean' U/Ca in these carbonates is 2.9 ng U mg(-1) Ca. This ratio, coupled with the assumption that all Ca in the Ganga-Indus headwaters is of carbonate origin and that U and Ca behave conservatively in rivers after their release from carbonates, provides an upper limit on the U contribution from these carbonates, to be a few percent of dissolved uranium in rivers. There are, however, a few streams with low uranium concentrations, for which the carbonate contribution could be much higher. These results suggest that Precambrian carbonates make only minor contributions to the uranium budget of the Ganga-Indus headwaters in the Himalaya on a basin wide scale, however, they could be important for particular streams. Similar estimates of silicate contribution to uranium budget of these rivers using U/Na in silicates and Na* (Na corrected for cyclic and halite contributions) in river waters show that silicates can contribute significantly (approximately 40% on average) to their U balance. If, however, much of the uranium in these silicates is associated with weathering resistant minerals, then the estimated silicate uranium component would be upper limits. Uranium concentration in black shales averages about 37 microg g(-1). Based on this concentration, supply of U from at least approximately 50 mg of black shales per liter of river water is needed to balance the average river water U concentration, 1.7 microg L

  14. Biological availability of (238)U, (234)U and (226)Ra for wild berries and meadow grasses in natural ecosystems of Belarus.

    Science.gov (United States)

    Sokolik, G A; Ovsiannikova, S V; Voinikava, K V; Ivanova, T G; Papenia, M V

    2014-01-01

    This work is devoted to investigation of behavior of (234)U, (238)U and (226)Ra by determining the soil to plant transfer under different natural conditions such as forest or swamped areas and meadow lands with different soil types. The paper summarizes the data on investigation of uranium and radium uptake by wild berries and natural meadow grasses in the typical conditions of Belarus. Parameters characterizing the biological availability of (234)U, (238)U and (226)Ra for bilberry (Vaccinium myrtillus), lingonberry (Vaccinium viti-idaea), blueberry (Vaccinium iliginosum) and cranberry (Vaccinium oxycoccus palustris) as well as for widely occurring mixed meadow vegetation, which belongs to the sedge-grass or grass-sedge associations and forbs, have been established. In the sites under investigation, the deposition levels of (238+239+240)Pu were less than 0.37 kBq m(-2) and (137)Cs deposition ranged between less than 0.37 and 37 kBq m(-2). It was found that activity concentrations of radionuclides in berries varied in the ranges of 0.037-0.11 for (234)U, 0.036-0.10 for (238)U and 0.11-0.43 Bq kg(-1) for (226)Ra, but in the mixed meadow grasses they were 0.32-4.4, 0.24-3.9 and 0.14-6.9 Bq kg(-1) accordingly. The (234)U/(238)U activity ratios were 1.02 ± 0.01 for wild berries, 1.20 ± 0.09 for underground meadow grasses and 1.02 ± 0.02 for proper soils. The concentration ratios (CRs, dry weight basis) of (234)U and (238)U for mixed meadow grasses were 0.036-0.42 and 0.041-0.46 respectively. The correspondent geometric means (GM) were 0.13 and 0.15 with geometric standard deviations (GSD) of 2.4. The CRs of (226)Ra for meadow grasses were 0.031-1.0 with GM 0.20 and GSD 2.6. The CRs of (234)U, (238)U and (226)Ra for wild berries ranged within 0.0018-0.008 (GM is 0.0034, GSD is 1.8), 0.0018-0.008 (GM is 0.0035, GSD is 1.8) and 0.005-0.033 (GM is 0.016, GSD is 2.1) accordingly. The highest CR values of uranium for mixed meadow grasses were found in the

  15. Determination of {sup 234}U and {sup 238}U activity concentrations in groundwaters from three deep wells drilled in Itu Intrusive Suite (SP); Determinacao das concentracoes de atividade de {sup 234}U e {sup 238}U em aguas subterraneas de tres pocos perfurados em rochas da Suite Intrusiva de Itu (SP)

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Francisca de

    2006-07-01

    Activity concentrations of ({sup 234}U) and ({sup 238}U) were determined in groundwaters drawn from three deep wells drilled in rocks from Itu Intrusive Suite (SP), two located in Salto town (S and SY wells) and the other one in Itu (I well). Sampling was done from September, 2004 to December, 2005, and twelve samples of each well were collected monthly. For those determinations alpha spectrometry technique was used, providing high precision results, as shown by the very good agreement of the data obtained in the analyses of 23 duplicates. The waters from the three wells presented a considerable enrichment of {sup 234}U in relation to {sup 238}U, indicating an important radioactive disequilibrium of these isotopes. In well I, the activity concentrations of ({sup 238}U) varied from (1,06 +- 0,03) to (2,1+- 0,2) mBq/L and those of ({sup 234}U) spanned from (3,1 +- 0,2) to (6,0 +- 0,4) mBq/L, whereas ({sup 234}U/{sup 238}U) activity ratios did not present significant variation, during the sampling time interval, presenting an average of 2,8 +- 0,1. The S waters showed the lowest uranium concentrations and the largest diversity of ({sup 238}U) and ({sup 234}U) activity concentrations, which varied from (0,26 +- 0,02) to (1,07+- 0,08) mBq/L and from (1,8 +- 0,1) to (7,0 +- 0,5) mBq/L, respectively, and also presented variable ({sup 234}U/{sup 238}U) activity ratios, spanning from (2,79 +- 0,07) to (8,1+- 0,3). In SY well, ({sup 238}U) activities varied between (0,8 +- 0,1) and (4,2 +- 0,3) mBq/L and those ones of ({sup 234}U) from (14 +- 1) to (53 +- 4) mBq/L, whereas ({sup 234}U/{sup 238}U) ratios fell in the interval from 12,6 +- 0,3 to 18,3 +- 0,4, with the highest activities of both radioisotopes registered during the dry season and the lowest ones in the rainy time period. The ({sup 234}U/{sup 238}U) activity ratios, which were invariable during sampling period of well I, indicated the contribution of rainfall to recharge the aquifer. The observed correlation

  16. The radiochemical contamination (210Po and 238U of zone around phosphogypsum waste heap in Wiślinka (northern Poland

    Directory of Open Access Journals (Sweden)

    Boryło A.

    2013-04-01

    Full Text Available The aim of this work was the determination of the impact of phosphogypsum waste heap in Wiślinka (northern Poland for radiological protection of zone around waste heap. The activity of 210Po, 234U, and 238U were measured using an alpha spectrometer. The values of uranium and polonium concentration in water with immediate area of waste heap are considerably higher than in the waters of the Martwa Wisła river. The values of activity ratio 234U/238U are approximately about one in the phosphogypsum (0.97±0.05 and in the water of retention reservoir and pumping station (0.92±0.01 and 0.99±0.08, while in the water from the Martwa Wisła river they are slightly higher than one (1.03±0.07 and 1.17±0.06. In the analyzed plants species the highest amounts of polonium and uranium were found in ruderal plants samples as well as hygrophilous plant samples. The more amounts of 210Po and 238U radionuclides were accumulated mainly in the roots of the analyzed plant species. The significant source of polonium and uranium in the natural environment is dry and wet atmospheric fallout in the immediate vicinity of phosphogypsum waste heap and the transfer via root for distant areas. The general conclusion of realized study is higher influence of phosphogypsum on radioactive contamination of environmental zone around heap waste in Wiślinka (northern Poland.

  17. Exploratory study of fission product yields of neutron-induced fission of 235U , 238U , and 239Pu at 8.9 MeV

    Science.gov (United States)

    Bhatia, C.; Fallin, B. F.; Gooden, M. E.; Howell, C. R.; Kelley, J. H.; Tornow, W.; Arnold, C. W.; Bond, E.; Bredeweg, T. A.; Fowler, M. M.; Moody, W.; Rundberg, R. S.; Rusev, G. Y.; Vieira, D. J.; Wilhelmy, J. B.; Becker, J. A.; Macri, R.; Ryan, C.; Sheets, S. A.; Stoyer, M. A.; Tonchev, A. P.

    2015-06-01

    Using dual-fission chambers each loaded with a thick (200 -400 -mg /c m2) actinide target of 235 ,238U or 239Pu and two thin (˜10 -100 -μ g /c m2) reference foils of the same actinide, the cumulative yields of fission products ranging from 92Sr to 147Nd have been measured at En= 8.9 MeV . The 2H(d ,n ) 3He reaction provided the quasimonoenergetic neutron beam. The experimental setup and methods used to determine the fission product yield (FPY) are described, and results for typically eight high-yield fission products are presented. Our FPYs for 235U(n ,f ) , 238U(n ,f ) , and 239Pu(n ,f ) at 8.9 MeV are compared with the existing data below 8 MeV from Glendenin et al. [Phys. Rev. C 24, 2600 (1981), 10.1103/PhysRevC.24.2600], Nagy et al. [Phys. Rev. C 17, 163 (1978), 10.1103/PhysRevC.17.163], Gindler et al. [Phys. Rev. C 27, 2058 (1983), 10.1103/PhysRevC.27.2058], and those of Mac Innes et al. [Nucl. Data Sheets 112, 3135 (2011), 10.1016/j.nds.2011.11.009] and Laurec et al. [Nucl. Data Sheets 111, 2965 (2010), 10.1016/j.nds.2010.11.004] at 14.5 and 14.7 MeV, respectively. This comparison indicates a negative slope for the energy dependence of most fission product yields obtained from 235U and 239Pu , whereas for 238U the slope issue remains unsettled.

  18. Trace element distribution and 235U/238U ratios in Euphrates waters and in soils and tree barks of Dhi Qar province (southern Iraq).

    Science.gov (United States)

    Riccobono, Francesco; Perra, Guido; Pisani, Anastasia; Protano, Giuseppe

    2011-09-01

    To assess the quality of the environment in southern Iraq after the Gulf War II, a geochemical survey was carried out. The survey provided data on the chemistry of Euphrates waters, as well as the trace element contents, U and Pb isotopic composition, and PAH levels in soil and tree bark samples. The trace element concentrations and the (235)U/(238)U ratio values in the Euphrates waters were within the usual natural range, except for the high contents of Sr due to a widespread presence of gypsum in soils of this area. The trace element contents in soils agreed with the common geochemistry of soils from floodplain sediments. Some exceptions were the high contents of Co, Cr and Ni, which had a natural origin related to ophiolitic outcrops in the upper sector of the Euphrates basin. The high concentrations of S and Sr were linked to the abundance of gypsum in soils. A marked geochemical homogeneity of soil samples was suggested by the similar distribution pattern of rare earth elements, while the (235)U/(238)U ratio was also fairly homogeneous and within the natural range. The chemistry of the tree bark samples closely reflected that of the soils, with some notable exceptions. Unlike the soils, some tree bark samples had anomalous values of the (235)U/(238)U ratio due to mixing of depleted uranium (DU) with the natural uranium pool. Moreover, the distribution of some trace elements (such as REEs, Th and Zr) and the isotopic composition of Pb in barks clearly differed from those of the nearby soils. The overall results suggested that significant external inputs occurred implying that once formed the DU-enriched particles could travel over long distances. The polycyclic aromatic hydrocarbon concentrations in tree bark samples showed that phenanthrene, fluoranthene and pyrene were the most abundant components, indicating an important role of automotive traffic.

  19. Evaluation of fission cross sections and covariances for {sup 233}U, {sup 235}U, {sup 238}U, {sup 239}Pu, {sup 240}Pu, and {sup 241}Pu

    Energy Technology Data Exchange (ETDEWEB)

    Kawano, Toshihiko [Kyushu Univ., Fukuoka (Japan); Matsunobu, Hiroyuki [Data Engineering, Inc. (Japan); Murata, Toru [AITEL Corporation, Tokyo (JP)] [and others

    2000-02-01

    A simultaneous evaluation code SOK (Simultaneous evaluation on KALMAN) has been developed, which is a least-squares fitting program to absolute and relative measurements. The SOK code was employed to evaluate the fission cross sections of {sup 233}U, {sup 235}U, {sup 238}U, {sup 239}Pu, {sup 240}Pu, and {sup 241}Pu for the evaluated nuclear data library JENDL-3.3. Procedures of the simultaneous evaluation and the experimental database of the fission cross sections are described. The fission cross sections obtained were compared with evaluated values given in JENDL-3.2 and ENDF/B-VI. (author)

  20. EXCALIBUR-at-CALIBAN: a neutron transmission experiment for {sup 238}U(n,n'{sub continuum}γ) nuclear data validation

    Energy Technology Data Exchange (ETDEWEB)

    Bernard, David; Leconte, Pierre; Destouches, Christophe [CEA, DEN, DER, SPRC et SPEX, Cadarache F-13108 SAINT-PAUL-LEZ-DURANCE (France); Casoli, Pierre; Chambru, Laurent; Chanussot, Didier; Chateauvieux, Herve; Gevrey, Gaetan; Guilbert, Frederique; Lereuil, Hugues; Rousseau, Guillaume; Schaub, Muriel [CEA, DAM, Valduc F-21120 IS-SUR-TILLE (France); Heusch, Murielle; Meplan, Olivier; Ramdhane, Mourad [CNRS/IN2P3, 53 rue des Martyrs, F-38026 Grenoble, Cedex (France)

    2015-07-01

    Two recent papers justified a new experimental program to give a new basis for the validation of {sup 238}U nuclear data, namely neutron induced inelastic scattering and transport codes at neutron fission energies. The general idea is to perform a neutron transmission experiment through natural uranium material. As shown by Hans Bethe, neutron transmissions measured by dosimetric responses are linked to inelastic cross sections. This paper describes the principle and the results of such an experience called EXCALIBUR performed recently (January and October 2014) at the CALIBAN reactor facility. (authors)

  1. Determination of environmental radioactivity (238U, 232Th and 40K) and indoor natural background radiation level in Chennai city (Tamilnadu State), India.

    Science.gov (United States)

    Babai, K S; Poongothai, S; Punniyakotti, J

    2013-01-01

    An extensive study on the determination of the natural radioactivity ((238)U, (232)Th and (40)K) levels in soil samples of Chennai city, India has been undertaken and the results of the same are compared with the levels reported in other Indian cities as well as other parts of the world. The radioactivity content in the soil samples, the absorbed dose rate, annual effective dose equivalent, radium equivalent activity, internal and external hazard indices were calculated and compared with UNSCEAR 2000 recommended values. In addition to the above, mapping of indoor natural background gamma radiation levels has been made using thermo luminescent dosemeters throughout Chennai city and the same are reported.

  2. 238U and 232Th series nuclides in groundwater from the J-13 well at the Nevada Test Site: Implications for ion retardation

    Science.gov (United States)

    Copenhaver, Sally A.; Krishnaswami, S.; Turekian, Karl K.; Shaw, Henry

    1992-07-01

    The activities of members of the 238U and 232Th decay chains have been determined in water from well J-13 at the Nevada Test Site near Yucca Mountain. Using 222Rn as a measure of recoil flux, adsorption (k1) and desorption (k2) rate constants for Ra and Pb have been determined. The ratio (k1/k2), defined as the dimensionless distribution coefficient, K, is 1.3 × 104 for Ra and 2.7 × 104 for Pb and is estimated to be about 104 for Th.

  3. Comparison of the (p,xn) cross sections from /sup 238/U, /sup 235/U, and /sup 232/Th targets irradiated with 200-MeV protons

    Energy Technology Data Exchange (ETDEWEB)

    Chu, Y.Y.; Zhou, M.L.

    1982-01-01

    We have measured absolute cross sections for (p,xn) reactions (x ranges from 0 to 8) from /sup 238/U, /sup 235/U, and /sup 232/Th targets irradiated with 200-MeV protons at the Brookhaven AGS Linac injector. Chemical yields were determined by using /sup 239/Np and /sup 233/Pa as tracers. Yield patterns obtained in this work can be compared to the experimental results and theoretical calculations from earlier work, and they are consistent within the framework of intranuclear cascade followed by neutron evaporation and fission competition.

  4. Accurate measurements of fission-fragment yields in 234,235,236,238U(γ,f with the SOFIA set-up

    Directory of Open Access Journals (Sweden)

    Chatillon A.

    2016-01-01

    Full Text Available SOFIA (Studies On Fission with Aladin is a new experimental set-up dedicated to accurate measurement of fission-fragments isotopic yields. It is located at GSI, the only place to use inverse kinematics at relativistic energies in order to study the (γ,f electromagnetic-induced fission. The SOFIA set-up is a large-acceptance magnetic spectrometer, which allows to fully identify both fission fragments in coincidence on the whole fission-fragment range. This paper will report on fission yields obtained in 234,235,236,238U(γ,f reactions.

  5. Investigations on the activity concentrations of 238U, 226RA, 228RA, 210PB and 40K in Jordan phosphogypsum and fertilizers.

    Science.gov (United States)

    Al-Jundi, J; Al-Ahmad, N; Shehadeh, H; Afaneh, F; Maghrabi, M; Gerstmann, U; Höllriegl, V; Oeh, U

    2008-01-01

    The activity concentrations of naturally occurring radionuclides ((238)U, (226)Ra, (228)Ra, (210)Pb and (40)K) in Jordanian phosphate ore, fertilizer material and phosphogypsum piles were investigated. The results show the partitioning of radionuclides in fertilizer products and phosphogypsum piles. The outcome of this study will enrich the Jordanian radiological map database, and will be useful for an estimation of the radiological impact of this industrial complex on the immediate environment. The activity concentration of (210)Pb was found to vary from 95 +/- 8 to 129 +/- 8 Bq kg(-1) with a mean value of 111 +/- 14 Bq kg(-1) in fertilizer samples, and from 364 +/- 8 to 428 +/- 10 Bq kg(-1) with a mean value of 391 +/- 30 Bq kg(-1) in phosphogypsum samples; while in phosphate wet rock samples, it was found to vary between 621 +/- 9 and 637 +/- 10 Bq kg(-1), with a mean value of 628 +/- 7 Bq kg(-1). The activity concentration of (226)Ra in fertilizer samples (between 31 +/- 4 and 42 +/- 5 Bq kg(-1) with a mean value of 37 +/- 6 Bq kg(-1)) was found to be much smaller than the activity concentration of (226)Ra in phosphogypsum samples (between 302 +/- 8 and 442 +/- 8 Bq kg(-1) with a mean value of 376 +/- 62 Bq kg(-1)). In contrast, the activity concentration of (238)U in fertilizer samples (between 1011 +/- 13 and 1061 +/- 14 Bq kg(-1) with a mean value of 1033 +/- 22 Bq kg(-1)) was found to be much higher than the activity concentration of (238)U in phosphogypsum samples (between 14 +/- 5 and 37 +/- 7 Bq kg(-1) with a mean value of 22 +/- 11 Bq kg(-1)). This indicates that (210)Pb and (226)Ra show similar behaviour, and are concentrated in phosphogypsum piles. In addition, both isotopes enhanced the activity concentration in phosphogypsum piles, while (238)U enhanced the activity concentration in the fertilizer. Due to the radioactivity released from the phosphate rock processing plants into the environment, the highest collective dose commitment for the lungs

  6. A study on possible use of Urtica dioica (common nettle) plants as uranium ((234)U, (238)U) contamination bioindicator near phosphogypsum stockpile.

    Science.gov (United States)

    Olszewski, Grzegorz; Boryło, Alicja; Skwarzec, Bogdan

    The aim of this study was to determine uranium concentrations in common nettle (Urtica dioica) plants and corresponding soils samples which were collected from the area of phosphogypsum stockpile in Wiślinka (northern Poland). The uranium concentrations in roots depended on its concentrations in soils. Calculated BCF and TF values showed that soils characteristics and air deposition affect uranium absorption and that different uranium species have different affinities to U. dioica plants. The values of (234)U/(238)U activity ratio indicate natural origin of these radioisotopes in analyzed plants. Uranium concentration in plants roots is negatively weakly correlated with distance from phosphogypsum stockpile.

  7. Yields of neutron-rich isotopes around Z = 28 produced in 30 MeV proton-induced fission of 238U

    Science.gov (United States)

    Kruglov, K.; Andreyev, A.; Bruyneel, B.; Dean, S.; Franchoo, S.; Górska, M.; Helariutta, K.; Huyse, M.; Kudryavtsev, Yu.; Mueller, W. F.; Prasad, N. V. S. V.; Raabe, R.; Schmidt, K.-H.; Van Duppen, P.; Van Roosbroeck, J.; Van de Vel, K.; Weissman, L.

    Heavy 65-70Co, 68-74Ni, 70-76Cu and 74-81Ga isotopes were produced at the LISOL facility by means of 30 MeV proton-induced fission of 238U. Production rates were deduced and compared to two types of cross-section calculations: the empirical model (V. Rubchenya, private communication) and the PROFI code. Comparison with experimental data favors the latter model. Yields using different beam-target combinations and different energies are calculated and discussed.

  8. Origin of the {sup 238}U-{sup 230}Th disequilibrium in magmas from subduction zones: the Arenal example; Origine du desequilibre {sup 238}U-{sup 230}TH dans les magmas des zones de subduction: exemple de l`Arenal

    Energy Technology Data Exchange (ETDEWEB)

    Villemant, B. [Paris-6 Univ., 75 (France)

    1996-12-31

    The existence in some volcanic products of strong excess of {sup 238}U with respect to {sup 230}Th is one of the characteristics of volcanic arc magmas. These excesses are generally attributed to fluid additions inside mantellic sources before magma segregation, differentiation and eruption. These fluids should be linked to the dehydration of the subducted rocks. These hypotheses are essentially based on correlations between {sup 10}Be, {sup 87}Sr anomalies, Ba/La ratios and on the distribution of volcanic centers with respect to the subduction zone. Recent studies suggest an evolution of the composition of volcanic sources in Central America from a depleted mantle type (MORB) in the North (Nicaragua) to a less transformed enriched type (OIB) in the South (Costa Rica). The Arenal volcano belongs to a transition zone between these two types. The preliminary study of trace elements and {sup 238}U-{sup 230}Th disequilibria in recent volcanic products (1968-1993) indicates a more complex situation. At least two different mantle sources were successively involved characterized by different Th/La and La/Yb ratios and very different to the OIB type. Also most lavas are in equilibrium with {sup 238}U/{sup 232}Th ratios of about 1.2 to 1.3. However, in eruptive cycle, some lavas are characterized by a strong {sup 238}U excess with respect to {sup 230}Th with cannot be linked to the sources, even when modified by fluids in depth. These results are interpreted in terms of heterogeneities of mantle sources and low depths late interactions with hydrothermal fluids during eruptions. Abstract only. (J.S.). 2 refs.

  9. Seasonal variations of total {sup 234}Th and dissolved {sup 238}U concentration activities in surface water of Bransfield Strait, Antarctica, from March to October 2011

    Energy Technology Data Exchange (ETDEWEB)

    Lapa, Flavia V.; Oliveira, Joselene de; Costa, Alice M.R., E-mail: fvlapa@ipen.br, E-mail: jolivei@ipen.br, E-mail: lice_mrc@hotmail.com [Instituto de Pesquisas Energeticas e Nucleares (IPEN-CNEN/SP), Sao Paulo, SP (Brazil). Laboratorio de Radiometria Ambiental; Braga, Elisabete S., E-mail: edsbraga@usp.br [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil). Inst. Oceanografico. Lab. de Nutrientes, Micronutrientes e Tracos nos Oceanos

    2013-07-01

    In this study the naturally occurring radionuclides {sup 234}Th and {sup 238}U were used to investigate the magnitude of upper ocean particulate organic carbon export in Bransfield Strait, Southern Ocean. This region is the largest oceanic high-nitrate low-chlorophyll (HNLC) area in the world and is known to contribute to regulate of the atmospheric CO{sub 2} via the biological pump. Due to its different geochemical behavior in seawater, the resulting U/Th disequilibria can be easily used to constrain the transport rates of particles and reaction processes between solution and particulate phases. Sampling occurred during the summer (March and November) 2011. Total {sup 234}Th activities in surface seawater samples ranged from 1.3 to 3.7 dpm L{sup -1} (station EB 011) during March/11 campaign, while in October/11 total {sup 234}Th activity concentrations varied from 1.4 to 2.9 dpm L{sup -1}. Highest total {sup 234}Th activities were found late in the austral summer season. Activity concentrations of dissolved {sup 238}U in surface seawater varied from 2.1 to 2.4 dpm L{sup -1}. Taking into account all sampling stations established in March and October/11 the relative variability of total {sup 234}Th distribution was 22%. (author)

  10. 238U-234U activity ratio as tracer of waterpathway within the watershed substratum: evidence of U data from the Strengbach and Ringelbach research catchments (Vosges , France)

    Science.gov (United States)

    Chabaux, F.; Schaffhausen, Th.; Pierret, M.-C.; Ambroise, B.

    2012-04-01

    U activity ratios were measured in spring and source waters collected in two small research watersheds developed on granitic bedrocks in Vosges Mountains (Eastern France), i.e., the Strengbach (http://ohge.u-strasbg.fr) and the Ringelbach catchments. The data indicates a clear relationship between the emerging altitude of sources/springs in each slope of the watersheds, and the intensity of 234U-238U activity ratios in the waters. Such a relationship can be readily explained through a scenario assuming that U mobilization in these waters and their 234U enrichment (consequence of the alpha recoil process) are controlled by the duration of the water-pathway within the substratum of the watershed: longer water pathway within the watershed, longer duration of water-rock interaction and hence higher 234U enrichment in the source/spring waters. The immediate consequence of such an interpretation is that (234U/238U) activity ratio in surface waters, at least at the scale of such small and elemental watersheds, might be a geochemical tracer useful to constrain a key hydrological parameter which controls, at least partly, the nature and the intensity of water-rock interactions in the watershed, namely the water pathway within the watershed substratum. The data also suggests that U activity ratios could be also very relevant to constrain the contribution of deep waters within surface waters. Future developments in this domain will certainly confirm the interest of U activity ratio as hydrological tracer of the water-rock interactions.

  11. Initial Design Calculations for a Detection System that will Observe Resonant Excitation of the 680 keV state in 238U

    Energy Technology Data Exchange (ETDEWEB)

    Pruet, J; Hagmann, C

    2007-01-26

    We present calculations and design considerations for a detection system that could be used to observe nuclear resonance fluorescence in {sup 238}U. This is intended as part of an experiment in which a nearly monochromatic beam of light incident on a thin foil of natural uranium resonantly populates the state at 680 keV in {sup 238}U. The beam of light is generated via Compton upscattering of laser light incident on a beam of relativistic electrons. This light source has excellent energy and angular resolution. In the current design study we suppose photons emitted following de-excitation of excited nuclei to be observed by a segmented array of BGO crystals. Monte Carlo calculations are used to inform estimates for the design and performance of this detector system. We find that each detector in this array should be shielded by about 2 cm of lead. The signal to background ratio for each of the BGO crystals is larger than ten. The probability that a single detector observes a resonant photon during a single pulse of the light source is near unity.

  12. Transfer of {sup 238}U, {sup 230}Th, {sup 226}Ra, and {sup 210}Pb from soils to tree and shrub species in a Mediterranean area

    Energy Technology Data Exchange (ETDEWEB)

    Blanco Rodriguez, P. [Natural Radioactivity Group, Facultad de Ciencias, Universidad de Extremadura, Avda. de Elvas s/n, 06071 Badajoz (Spain); Vera Tome, F. [Natural Radioactivity Group, Facultad de Ciencias, Universidad de Extremadura, Avda. de Elvas s/n, 06071 Badajoz (Spain)], E-mail: fvt@unex.es; Lozano, J.C. [Natural Radioactivity Group, Facultad de Ciencias, Universidad de Extremadura, Avda. de Elvas s/n, 06071 Badajoz (Spain); Laboratorio de Radiaciones Ionizantes, Facultad de Ciencias, Universidad de Salamanca, 37008 Salamanca (Spain); Perez Fernandez, M.A. [Natural Radioactivity Group, Facultad de Ciencias, Universidad de Extremadura, Avda. de Elvas s/n, 06071 Badajoz (Spain); Area de Ecologia, Universidad Pablo Olavide, Carretera de Utrera km. 1, 41013 Sevilla (Spain)

    2010-06-15

    The soil-to-plant transfer factors of natural uranium isotopes ({sup 238}U and {sup 234}U), {sup 230}Th, {sup 226}Ra, and {sup 210}Pb were studied in a disused uranium mine located in the Extremadura region in the south-west of Spain. The plant samples included trees (Quercus ilex, Quercus suber, and Eucalyptus cameldulensis) and one shrub (Cytisus multiflorus). All of them are characteristic of Mediterranean environments. The activity concentrations in leaves and fruit were determined for the tree species at different stages of growth. For the shrub, the total above-ground fraction was considered in three seasons. For old leaves and fruit, the highest activity concentrations were found in Eucalyptus cameldulensis for all the radionuclides studied, except in the case of {sup 230}Th that presented similar activity concentrations in all of the tree species studied. In every case, the transfer to fruit was less than the transfer to leaves. In the shrub, the results depended on the season of sampling, with the highest value obtained in spring and the lowest in autumn. Important correlations were obtained for {sup 238}U and {sup 226}Ra between the activity ratio in soils with that in leaves or fruit.

  13. Determination of (238)U, (232)Th and (40)K activity concentrations in riverbank soil along the Chao Phraya river basin in Thailand.

    Science.gov (United States)

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

    2014-12-01

    The activity concentrations of (238)U, (232)Th and (40)K in riverbank soil along the Chao Phraya river basin was determined through gamma-ray spectrometry measurements made using a hyper-pure germanium detector in a low background configuration. The ranges of activity concentrations of (238)U, (232)Th and (40)K were found to be 13.9 ↔ 76.8, 12.9 ↔ 142.9 and 178.4 ↔ 810.7 Bq kg(-1), respectively. The anthropogenic radionuclide, (137)Cs, was not observed in statistically significant amounts above the background level in the current study. The absorbed gamma dose rate in air at 1 m above the ground surface, the outdoor annual effective dose equivalent, the values of the radium equivalent activity and the external hazard index associated with all the soil samples in the present work were evaluated. The results indicate that the radiation hazard from primordial radionuclides in all soil samples from the area studied in this current work is not significant.

  14. Characterization of {sup 238}U, {sup 232}Th, {sup 40}K, and {sup 226}Ra in NORM and Air Particulate Occurring from Phosphate Processing Facility

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Yoon Hee; Lim, Jong Myoung; Ji, Young Yong; Kim, Hyun Cheol; Kim, Chang Jong; Park, Ji Yong; Chung, Kun Ho; Kang, Mun Ja [KAERI, Daejeon (Korea, Republic of)

    2016-05-15

    In this study, radio-activities of {sup 238}U, {sup 232}Th, {sup 40}K, and {sup 226}Ra occurring in raw materials and by-products at phosphate processing facility were complementally determined using ED-XRF, γ-spectrometry and ICP-MS method. Although the degree of immersion in the human body varies depending on the particle size and density, the particle size is especially used as a key factor in assessing dose. Thus, size distribution characteristics of {sup 238}U concentrations in airborne particulates collected at the phosphate processing facility were also evaluated. The naturally occurring radioactive materials (NORM) are widely spread throughout the environment, it occupies the largest part of public radioactivity exposure. According to report of the US National Academy of Sciences, 82% of the human radiation dose received annually comes from the natural radionuclides. Radiation exposure doses from natural radionuclides is not significantly concerned level compared to those from artificial radionuclides which could be released into the environment by nuclear tests and power plant accident. It could make a serious risk problem to unspecific public when exposed to the natural radionuclides during long-term period at high activity concentration levels. Therefore, it is essential to make a professional and systematic approach for the proper handling and diminution.

  15. Measurements of yields of fission products in the reaction of {sup 238}U with high-energy p, d and n beams

    Energy Technology Data Exchange (ETDEWEB)

    Nolen, J.A.; Ahmad, I.; Back, B.B. [and others

    1995-08-01

    An experiment was performed at the Michigan State University cyclotron to determine the yields of neutron-rich fission products in the reaction of {sup 238}U with 100-MeV neutrons, 200-MeV deuterons and 200-MeV protons. Several 1-mm-thick {sup 238}U foils were irradiated for 100-second intervals sequentially for each configuration and the ten spectra were added for higher statistics. The three successive spectra, each for a 40 s period, were accumulated for each sample. Ten foils were irradiated. Successive spectra allowed us to determine approximate half-lives of the gamma peaks. Several arrangements, which were similar to the setup we plan to use in our radioactive beam proposal, were used for the production of fission products. For the high-energy neutron irradiation, U foils were placed after a 5-inch-long, 1-inch-diameter Be cylinder which stopped the 200-MeV deuteron beam generating 100-MeV neutrons. Arrangements for deuteron irradiation included direct irradiation of U foils, placing U foils after different lengths of (0.5 inch, 1.0 inch and 1.5 inch) 2-inch diameter U cylinder. Since the deuteron range in uranium is 17 mm, some of the irradiations were due to the secondary neutrons from the deuteron-induced fission of U. Similar arrangements were also used for the 200-MeV proton irradiation of the {sup 238}U foils. In all cases, several neutron-rich fission products were identified and their yields determined. In particular, we were able to observe Sn in all the runs and determine its yield. The data show that with our proposed radioactive device we will be able to produce more than 10{sup 12} {sup 132}Sn atoms per second in the target. Assuming an overall efficiency of 1 %, we will be able to deliver one particle nanoampere of {sup 132}Sn beam at a target location. Detailed analysis of the {gamma}-ray spectra is in progress.

  16. Identification of 45 New Neutron-Rich Isotopes Produced by In-Flight Fission of a 238U Beam at 345 MeV/nucleon

    OpenAIRE

    Ohnishi, Tetsuya; Kubo*, Toshiyuki; Kusaka, Kensuke; Yoshida, Atsushi; Yoshida, Koichi; Ohtake, Masao; Fukuda, Naoki; Takeda, Hiroyuki; Kameda, Daisuke; Tanaka, Kanenobu; Inabe, Naohito; Yanagisawa, Yoshiyuki; Gono, Yasuyuki; Watanabe, Hiroshi; Otsu, Hideaki

    2010-01-01

    A search for new isotopes using in-flight fission of a 345 MeV/nucleon 238U beam has been carried out at the RI Beam Factory at the RIKEN Nishina Center. Fission fragments were analyzed and identified by using the superconducting in-flight separator BigRIPS. We observed 45 new neutron-rich isotopes: 71Mn, 73,74Fe, 76Co, 79Ni, 81,82Cu, 84,85Zn, 87Ga, 90Ge, 95Se, 98Br, 101Kr, 103Rb, 106,107Sr, 108,109Y, 111,112Zr, 114,115Nb, 115,116,117Mo, 119,120Tc, 121,122,123,124Ru, 123,124,125,126Rh, 127,12...

  17. Experimental Neutron-Induced Fission Fragment Mass Yields of 232Th and 238U at Energies from 10 to 33 MeV

    CERN Document Server

    Simutkin, V D; Blomgren, J; Österlund, M; Bevilacqua, R; Ryzhov, I V; Tutin, G A; Yavshits, S G; Vaishnene, L A; Onegin, M S; Meulders, J P; Prieels, R

    2013-01-01

    Development of nuclear energy applications requires data for neutron-induced reactions for actinides in a wide neutron energy range. Here we describe measurements of pre-neutron emission fission fragment mass yields of 232Th and 238U at incident neutron energies from 10 to 33 MeV. The measurements were done at the quasi-monoenergetic neutron beam of the Louvain-la-Neuve cyclotron facility CYCLONE; a multi-section twin Frisch-gridded ionization chamber was used to detect fission fragments. For the peak neutron energies at 33, 45 and 60 MeV, the details of the data analysis and the experimental results have been published before and in this work we present data analysis in the low-energy tail of the neutron energy spectra. The preliminary measurement results are compared with available experimental data and theoretical predictions.

  18. High accuracy determination of the $^{238}$U/$^{235}$U fission cross section ratio up to $\\sim$1 GeV at n_TOF (CERN)

    CERN Document Server

    Paradela, C; Tarrío, D; Leal-Cidoncha, E; Leong, L S; Tassan-Got, L; Naour, C Le; Duran, I; Colonna, N; Audouin, L; Mastromarco, M; Meo, S Lo; Ventura, A; Altstadt, S; Andrzejewski, J; Barbagallo, M; Bécares, V; Bečvář, F; Belloni, F; Berthoumieux, E; Billowes, J; Boccone, V; Bosnar, D; Brugger, M; Calviño, F; Cano-Ott, D; Carrapiço, C; Cerutti, F; Chiaveri, E; Chin, M; Cortés, G; Cortés-Giraldo, M A; Cosentino, L; Diakaki, M; Domingo-Pardo, C; Dressler, R; Eleftheriadis, C; Ferrari, A; Finocchiaro, P; Fraval, K; Ganesan, S; García, A R; Giubrone, G; Gómez-Hornillos, M B; Gonçalves, I F; González-Romero, E; Griesmayer, E; Guerrero, C; Gunsing, F; Gurusamy, P; Heinitz, S; Jenkins, D G; Jericha, E; Käppeler, F; Karadimos, D; Kivel, N; Kokkoris, M; Krtička, M; Kroll, J; Langer, C; Lederer, C; Leeb, H; Losito, R; Manousos, A; Marganiec, J; Martínez, T; Massimi, C; Mastinu, P; Mendoza, E; Mengoni, A; Milazzo, P M; Mingrone, F; Mirea, M; Mondalaers, W; Musumarra, A; Pavlik, A; Perkowski, J; Plompen, A; Praena, J; Quesada, J; Rauscher, T; Reifarth, R; Riego, A; Roman, F; Rubbia, C; Sarmento, R; Saxena, A; Schillebeeckx, P; Schmidt, S; Schumann, D; Tagliente, G; Tain, J L; Tsinganis, A; Valenta, S; Vannini, G; Variale, V; Vaz, P; Versaci, R; Vermeulen, M J; Vlachoudis, V; Vlastou, R; Wallner, A; Ware, T; Weigand, M; Weiß, C; Wright, T; Žugec, P

    2015-01-01

    The $^{238}$U to $^{235}$U fission cross section ratio has been determined at n_TOF up to $\\sim$1 GeV, with two different detection systems, in different geometrical configurations. A total of four datasets have been collected and compared. They are all consistent to each other within the relative systematic uncertainty of 3-4%. The data collected at n_TOF have been suitably combined to yield a unique fission cross section ratio as a function of the neutron energy. The result confirms current evaluations up to 200 MeV. A good agreement is also observed with theoretical calculations based on the INCL++/Gemini++ combination up to the highest measured energy. The n_TOF results may help solving a long-standing discrepancy between the two most important experimental dataset available so far above 20 MeV, while extending the neutron energy range for the first time up to $\\sim$1 GeV.

  19. Fission Product Yields of 233U, 235U, 238U and 239Pu in Fields of Thermal Neutrons, Fission Neutrons and 14.7-MeV Neutrons

    Science.gov (United States)

    Laurec, J.; Adam, A.; de Bruyne, T.; Bauge, E.; Granier, T.; Aupiais, J.; Bersillon, O.; Le Petit, G.; Authier, N.; Casoli, P.

    2010-12-01

    The yields of more than fifteen fission products have been carefully measured using radiochemical techniques, for 235U(n,f), 239Pu(n,f) in a thermal spectrum, for 233U(n,f), 235U(n,f), and 239Pu(n,f) reactions in a fission neutron spectrum, and for 233U(n,f), 235U(n,f), 238U(n,f), and 239Pu(n,f) for 14.7 MeV monoenergetic neutrons. Irradiations were performed at the EL3 reactor, at the Caliban and Prospero critical assemblies, and at the Lancelot electrostatic accelerator in CEA-Valduc. Fissions were counted in thin deposits using fission ionization chambers. The number of fission products of each species were measured by gamma spectrometry of co-located thick deposits.

  20. Identification of 45 New Neutron-Rich Isotopes Produced by In-Flight Fission of a 238U Beam at 345 MeV/nucleon

    CERN Document Server

    Ohnishi, Tetsuya; Kusaka, Kensuke; Yoshida, Atsushi; Yoshida, Koichi; Ohtake, Masao; Fukuda, Naoki; Takeda, Hiroyuki; Kameda, Daisuke; Tanaka, Kanenobu; Inabe, Naohito; Yanagisawa, Yoshiyuki; Gono, Yasuyuki; Watanabe, Hiroshi; Otsu, Hideaki; Baba, Hidetada; Ichihara, Takashi; Yamaguchi, Yoshitaka; Takechi, Maya; Nishimura, Shunji; Ueno, Hideki; Yoshimi, Akihiro; Sakurai, Hiroyoshi; Motobayashi, Tohru; Nakao, Taro; Mizoi, Yutaka; Matsushita, Masafumi; Ieki, Kazuo; Kobayashi, Nobuyuki; Tanaka, Kana; Kawada, Yosuke; Tanaka, Naoki; Deguchi, Shigeki; Satou, Yoshiteru; Kondo, Yosuke; Nakamura, Takashi; Yoshinaga, Kenta; Ishii, Chihiro; Yoshii, Hideakira; Miyashita, Yuki; Uematsu, Nobuya; Shiraki, Yasutsugu; Sumikama, Toshiyuki; Chiba, Junsei; Ideguchi, Eiji; Saito, Akito; Yamaguchi, Takayuki; Hachiuma, Isao; Suzuki, Takeshi; Moriguchi, Tetsuaki; Ozawa, Akira; Ohtsubo, Takashi; Famiano, Michael A; Geissel, Hans; Nettleton, Anthony S; Tarasov, Oleg B; Bazin, Daniel P; Sherrill, Bradley M; Manikonda, Shashikant L; Nolen, Jerry A

    2010-01-01

    A search for new isotopes using in-flight fission of a 345 MeV/nucleon 238U beam has been carried out at the RI Beam Factory at the RIKEN Nishina Center. Fission fragments were analyzed and identified by using the superconducting in-flight separator BigRIPS. We observed 45 new neutron-rich isotopes: 71Mn, 73,74Fe, 76Co, 79Ni, 81,82Cu, 84,85Zn, 87Ga, 90Ge, 95Se, 98Br, 101Kr, 103Rb, 106,107Sr, 108,109Y, 111,112Zr, 114,115Nb, 115,116,117Mo, 119,120Tc, 121,122,123,124Ru, 123,124,125,126Rh, 127,128Pd, 133Cd, 138Sn, 140Sb, 143Te, 145I, 148Xe, and 152Ba.

  1. Ground water contamination with (238)U, (234)U, (235)U, (226)Ra and (210)Pb from past uranium mining: cove wash, Arizona.

    Science.gov (United States)

    Dias da Cunha, Kenya Moore; Henderson, Helenes; Thomson, Bruce M; Hecht, Adam A

    2014-06-01

    The objectives of the study are to present a critical review of the (238)U, (234)U, (235)U, (226)Ra and (210)Pb levels in water samples from the EPA studies (U.S. EPA in Abandoned uranium mines and the Navajo Nation: Red Valley chapter screening assessment report. Region 9 Superfund Program, San Francisco, 2004, Abandoned uranium mines and the Navajo Nation: Northern aum region screening assessment report. Region 9 Superfund Program, San Francisco, 2006, Health and environmental impacts of uranium contamination, 5-year plan. Region 9 Superfund Program, San Franciso, 2008) and the dose assessment for the population due to ingestion of water containing (238)U and (234)U. The water quality data were taken from Sect. "Data analysis" of the published report, titled Abandoned Uranium Mines Project Arizona, New Mexico, Utah-Navajo Lands 1994-2000, Project Atlas. Total uranium concentration was above the maximum concentration level for drinking water (7.410-1 Bq/L) in 19 % of the water samples, while (238)U and (234)U concentrations were above in 14 and 17 % of the water samples, respectively. (226)Ra and (210)Pb concentrations in water samples were in the range of 3.7 × 10(-1) to 5.55 × 102 Bq/L and 1.11 to 4.33 × 102 Bq/L, respectively. For only two samples, the (226)Ra concentrations exceeded the MCL for total Ra for drinking water (0.185 Bq/L). However, the (210)Pb/(226)Ra ratios varied from 0.11 to 47.00, and ratios above 1.00 were observed in 71 % of the samples. Secular equilibrium of the natural uranium series was not observed in the data record for most of the water samples. Moreover, the (235)U/(total)U mass ratios ranged from 0.06 to 5.9 %, and the natural mass ratio of (235)U to (total)U (0.72 %) was observed in only 16 % of the water samples, ratios above or below the natural ratio could not be explained based on data reported by U.S. EPA. In addition, statistical evaluations showed no correlations among the distribution of the radionuclide concentrations

  2. EFFECTIVE SPECIFIC ACTIVITY OF NATURAL RADIONUCLIDES FOR THE NORM BELONGED TO 238U AND 232TH SERIES BEING IN THE STATE OF DISTURBED RADIOACTIVE EQUILIBRIUM

    Directory of Open Access Journals (Sweden)

    I. P. Stamat

    2008-01-01

    Full Text Available In the Sanitary Rules SR 2.6.1.1292-03 and SR 2.6.6.1169-02 classification of the industrial waste containing naturally occurring radioactive materials is adopted in accordance to the values of their effective specific activity Aeff. In a case of the disturbed equilibrium in 238U and 232Th series it is necessary to take into consideration actual contribution of the separate natural radionuclides of the mentioned series into the value of gamma dose rate of the waste. This will permit to avoid unjustified overestimating or understating of the waste category which prevents as unjustified expenditures on their treating so undertaking of the necessary measures providing radiation safety.

  3. (238)U/(235)U isotope ratios of crustal material, rivers and products of hydrothermal alteration: new insights on the oceanic U isotope mass balance.

    Science.gov (United States)

    Noordmann, Janine; Weyer, Stefan; Georg, R Bastian; Jöns, Svenja; Sharma, Mukul

    2016-01-01

    In this study, the U isotope composition, n((238)U)/n((235)U), of major components of the upper continental crust, including granitic rocks of different age and post-Archaean shales, as well as that of rivers (the major U source to the oceans) was investigated. Furthermore, U isotope fractionation during the removal of U at mid-ocean ridges, an important sink for U from the oceans, was investigated by the analyses of hydrothermal water samples (including low- and high-temperature fluids), low-temperature altered basalts and calcium carbonate veins. All analysed rock samples from the continental crust fall into a limited range of δ(238)U between -0.45 and -0.21 ‰ (relative to NBL CRM 112-A), with an average of -0.30 ± 0.15 ‰ (2 SD, N = 11). Despite differences in catchment lithologies, all major rivers define a relatively narrow range between -0.31 and -0.13 ‰, with a weighted mean isotope composition of -0.27 ‰, which is indistinguishable from the estimate for the upper continental crust (-0.30 ‰). Only some tributary rivers from the Swiss Alps display a slightly larger range in δ(238)U (-0.29 to +0.01 ‰) and lower U concentrations (0.87-3.08 nmol/kg) compared to the investigated major rivers (5.19-11.69 nmol/kg). These findings indicate that only minor net U isotope fractionation occurs during weathering and transport of material from the continental crust to the oceans. Altered basalts display moderately enriched U concentrations (by a factor of 3-18) compared to those typically observed for normal mid-ocean ridge basalts. These, and carbonate veins within altered basalts, show large U isotope fractionation towards both heavy and light U isotope compositions (ranging from -0.63 to +0.27 ‰). Hydrothermal water samples display low U concentrations (0.3-1 nmol/kg) and only limited variations in their U isotope composition (-0.43 ± 0.25 ‰) around the seawater value. Nevertheless, two of the investigated fluids display

  4. Separation and quantification of {sup 238}U, {sup 232}Th and rare earths in monazite samples by ion chromatography coupled with on-line flow scintillation detector

    Energy Technology Data Exchange (ETDEWEB)

    Borai, E.H.; Mady, A.S

    2002-10-01

    An alternative procedure has been described for efficient separation and quantitative determination of uranium (U), thorium (Th) and rare earth elements (REEs) in monazite mineral by high performance ion chromatographic system (IC). Different variables affecting the distribution coefficient, the retention and hence separation efficiency such as eluent flow rate and concentrations of HCl and ammonium sulfate (NH{sub 4}){sub 2}SO{sub 4} containing the mobile phase were studied. The developed separation protocol of U, Th and REEs was optimized using an Ion Pac CS5 separation column followed by post-column derivatization reaction with Arsenaso III and UV-VIS spectrophotometeric detection. Comparative evaluation of U, Th and REEs concentration in monazite mineral was demonstrated using two different on-line detection modes including flow through cell scintillation detector (FSD) and UV-VIS spectrophotometer. Response of the FSD was found to be linear over the full range of activities investigated (4-100 Bq). The lower limits of detection (LLD) for the investigated radionuclides were 3.0{+-}0.1 Bq for {sup 238}U and 6.0{+-}0.1 Bq for {sup 232}Th. The detection of {sup 238}U and {sup 232}Th by FSD shows good agreement with the corresponding determination by UV-VIS spectrophotometer. The content of ThO{sub 2} and U{sub 3}O{sub 8} in monazite sample were found to be 4.7{+-}0.1% and 0.42{+-}0.04% using UV-VIS detector and 4.3{+-}0.1% and 0.45{+-}0.1% using FSD, respectively.

  5. The cumulative effect of three decades of phosphogypsum amendments in reclaimed marsh soils from SW Spain: (226)Ra, (238)U and Cd contents in soils and tomato fruit.

    Science.gov (United States)

    Abril, José-María; García-Tenorio, Rafael; Enamorado, Santiago M; Hurtado, M Dolores; Andreu, Luis; Delgado, Antonio

    2008-09-15

    Phosphogypsum (PG), a by-product of the phosphate fertiliser industries, has been applied as soil amendment to reduce Na saturation in soils, as in the reclaimed marsh area from SW Spain, where available PG has a typical fingerprint of 710+/-40 Bq kg(-1) of (226)Ra, 165+/-15 Bq kg(-1) of (238)U and 2.8+/-0.4 mg kg(-1) of Cd. This work was focussed on the cumulative effects of PG amendments on the enrichment of these pollutants in cultivated soils and plants (Lycopersicum esculentum Mill L.) from the area studied, where PG has been applied since 1978 at recommended rates of 20-25 Mg ha(-1) every 2-3 years. A field experiment was conducted over three years to compare activity concentrations of (226)Ra ((214)Pb) and (238)U ((234)Th) in non-reclaimed soils, reclaimed soils with no additional PG application, and reclaimed soils with two additional PG applications. A non-significant effect of two PG amendments (in three years) was observed when compared with non-amended reclaimed plots. Nevertheless, a significant (p<0.05) enrichment of (226)Ra was observed in the surface horizon (0-30 cm) of reclaimed plots relative to deeper horizons and also when compared with the surface horizon of non-reclaimed soil (p<0.05), thereby revealing the cumulative effect of three decades of PG applications. Furthermore, the effect of a continuous application of PG was studied by analysing soils and tomato fruits from six commercial farms with different cumulative rates of PG applied. Cadmium concentrations in tomatoes, which were one order of magnitude higher than those found in tomatoes from other areas in South Spain, were positively correlated (r = 0.917) with (226)Ra-concentration in soils, which can be considered an accurate index of the cumulative PG rate of each farm.

  6. The influence of the nature of soil and plant and pollution on the 238U, 232Th, 222Rn and 220Rn concentrations in various natural honey samples using nuclear track detectors: Impact on the adult consumers

    Indian Academy of Sciences (India)

    M A Misdaq; A Mortassim

    2009-11-01

    238U and 232Th concentrations as well as 222Rn and 220Rn -activities per unit volume were measured in various natural honey samples collected from different regions in Morocco using CR-39 and LR-115 type II solid state nuclear track detectors (SSNTDs). These radionuclides were also measured in soils, plant flowers and nectar solutions corresponding to the honey samples studied. In addition, these radionuclides were measured in different imported honey samples. The measured 238U, 232Th, 222Rn and 220Rn concentrations ranged from (1.5 ± 0.1) mBq kg-1 to (10.6 ± 0.6) mBq kg-1, (1.1 ± 0.1) mBq kg-1 to (4.2 ± 0.2) mBq kg-1 , (1.5 ± 0.1) Bq kg-1 to (10.6 ± 0.6) Bq kg-1 and (1.1 ± 0.1) Bq kg-1 to (4.2 ± 0.2) Bq kg-1 for the honey samples studied, respectively. Annual 238U, 232Th and 222Rn intakes by Moroccan adults from the consumption of honey were assessed. The influence of the nature of soil and plant on the 238U and 232Th contents of the studied honey samples was investigated. These measurements were completed by an investigation of the 238U and 232 Th transfer between soils and plant flowers and that between plant flowers and honey, and also by the investigation of the influence of pollution due to different material dusts on 238U, 232Th and 222Rn in the honey samples studied. Committed equivalent doses due to the annual intake of 238U, 232Th and 222Rn were evaluated in the organs of adult members of the Moroccan rural population from the ingestion of the honey samples. The maximum total committed effective dose due to 238U, 232Th and 222Rn from the ingestion of natural honey by the Moroccan rural population was found to be equal to 0.64 Sv y-1 .

  7. CREATING THE KULTUK POLYGON FOR EARTHQUAKE PREDICTION: VARIATIONS OF (234U/238U) AND 87SR/86SR IN GROUNDWATER FROM ACTIVE FAULTS AT THE WESTERN SHORE OF LAKE BAIKAL

    OpenAIRE

    S. V. Rasskazov; E. P. Chebykin; A. M. Ilyasova; E. N. Vodneva; I. S. Chuvashova; Bornyakov, S. A.; A. K. Seminsky; S. V. Snopkov; V. V. Chechel'nitsky; N. A. Gileva

    2015-01-01

    Introduction. Determinations of (234U/238U) in groundwater samples are used for monitoring current deformations in active faults (parentheses denote activity ratio units). The cyclic equilibrium of activity ratio 234U/238U≈≈(234U/238U)≈γ≈1 corresponds to the atomic ratio ≈5.47×10–5. This parameter may vary due to higher contents of 234U nuclide in groundwater as a result of rock deformation. This effect discovered by P.I. Chalov and V.V. Cherdyntsev was described in [Cherdyntsev, 1969, 1973; ...

  8. Use of LabSOCS for determination of specific concentrations of {sup 40}K, {sup 238}U and {sup 232}Th in fertilizer samples; Uso de LabSOCS no calculo da eficiencia de detecao para determinacao da concentracao especifica de {sup 40}K, {sup 238}U e {sup 232}Th em amostras de fertilizantes

    Energy Technology Data Exchange (ETDEWEB)

    Garcez, Ricardo Washington Dutra; Lopes, Jose Marques; Silva, Ademir Xavier da, E-mail: rgarcez@con.ufrj.br, E-mail: marqueslopez@yahoo.com.br [Coordenacao dos Programas de Pos-Graduacao em Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Programa de Engenharia Nuclear; Domingues, Alessandro Mariano; Lima, Marco Frota, E-mail: slessandrodomingues@fisica.if.uff.br, E-mail: marcofrotalima@yahoo.com.br [Universidade Federal Fluminense (UFF), Niteroi, RJ (Brazil). Instituto de Biologia

    2015-07-01

    Use of fertilizer is an established practice worldwide to promote agricultural productivity increased without increasing the planted area, resulting in native forests protection and increase of the food availability. Some kinds of fertilizer have in their chemical composition some radionuclides due the origin of its feedstock, such as {sup 238}U, the {sup 232}Th, and their descendants, beyond {sup 40}K. Knowledge of the radioactivity levels in the environment is great importance to know the gamma radiation dose that the human being is exposed. For identification and quantitation of radionuclides, it was used gamma spectrometry where HPGe detector was used to obtain the spectra, and LabSOCS software for calculating the detection efficiency for each energy. The values of {sup 232}Th specific concentrations ranged from 4.1 to 368.1 Bq.Kg{sup -1} , the values of {sup 238}U specific concentrations ranged from 16.0 to 647.7 Bq.Kg{sup -1} and {sup 40}K specific concentrations ranged from 19.1 to 12713 Bq.Kg{sup -1} . Concentrations of values are consistent with those found in literature. (author)

  9. Uranium isotopic ratio measurements ({sup 235}U/{sup 238}U) by laser ablation high resolution inductively coupled plasma mass spectrometry for environmental radioactivity monitoring - {sup 235}U/{sup 238}U isotope ratio analysis by LA-ICP-MS-HR for environmental radioactivity monitoring

    Energy Technology Data Exchange (ETDEWEB)

    David, K.; Mokili, M.B.; Rousseau, G.; Deniau, I.; Landesman, C. [SUBATECH, Ecole des Mines de Nantes, Universite de Nantes, CNRS/IN2P3, 4 rue Alfred Kastler, 44307 Nantes cedex 3 (France)

    2014-07-01

    The protection of the aquatic and terrestrial environments from a broad range of contaminants spread by nuclear activities (nuclear plants, weapon tests or mining) require continuous monitoring of long-lives radionuclides that were released into the environment. The precise determination of uranium isotope ratios in both natural and potential contaminated samples is of primary concern for the nuclear safeguards and the control of environmental contamination. As an example, analysis of environmental samples around nuclear plants are carried out to detect the traces in the environment originating from nuclear technology activities. This study deals with the direct analysis of {sup 235}U/{sup 238}U isotope ratios in real environmental solid samples performed with laser ablation (LA)-HR-ICP-MS. A similar technique has already been reported for the analysis of biological samples or uranium oxide particles [1,2] but to our knowledge, this was never applied on real environmental samples. The high sensitivity, rapid acquisition time and low detection limits are the main advantages of high resolution ICP-MS for accurate and precise isotope ratio measurements of uranium at trace and ultra-trace levels. In addition, the use of laser ablation allows the analysis of solid samples with minimal preparation. A a consequence, this technique is very attractive for conducting rapid direct {sup 235}U/{sup 238}U isotope ratio analysis on a large set of various matrix samples likely to be encountered in environmental monitoring such as corals, soils, sands, sediments, terrestrial and marine bio-indicators. For the present study, LA-ICP-MS-HR analyses are performed using a New Wave UP213 nano-second Nd:YAG laser coupled to a Thermo Element-XR high resolution mass spectrometer. Powdered samples are compacted with an hydraulic press (5 tons) in order to obtain disk-shaped pellet (10-13 mm in diameter and 2 mm in thickness). The NIST612 reference glass is used for LA-ICP-MS-HR tuning and as

  10. Transfer Rates of 238U and 232Th for E. globulus, A. mearnsii, H. filipendula and Hazardous Effects of the Usage of Medicinal Plants From Around Gold Mine Dump Environs

    Directory of Open Access Journals (Sweden)

    Victor M. Tshivhase

    2015-12-01

    Full Text Available Medicinal plant consumption can be a source of human exposure to radioactive elements such as 238U and 232Th, which can lead to internal radiation doses. The uptake of 238U and 232Th from soils to the leaf samples of three different medicinal plant species (Eucalyptus globulus, Acacia mearnsii and Hyparrhenia filipendula from the purlieu of the Princess gold mine dump, an abandoned contaminated tailings storage site (TSS, located at longitude 27°55′00″E and latitude 26°09′30″S in Davidsonville (Roodepoort, west of Johannesburg, South Africa was measured. This was done using ICP-MS spectrometry and substantial differences were observed in the soil-plant transfer factor (TF values between these radionuclides. The plant species E. globulus exhibited the highest uptake of 238U, with an average TF of 3.97, while that of H. filipendula was 0.01 and the lowest TF of 0.15 × 10−2 was measured for A. mearnsii. However, in the case of 232Th, the highest average TF was observed for A. mearnsii (0.29, followed by E. globulus (0.10 and lowest was measured for H. filipendula (0.27 × 10−2. The ratio of TF average value i.e., 238U to 232Th in the soil-plant leaves was 38.05 for E. globulus, 0.01 for A. mearnsii and 4.38 for H. filipendula.

  11. The study of the (α, α'f) reaction at 120 MeV on 232Th and 238U (II) : Fission barrier properties deduced from fission probabilities and angular distributions

    NARCIS (Netherlands)

    Plicht, J. van der; Harakeh, M.N.; van der Woude, Adriaan; David, P.; Debrus, J.; Janszen, H.; Schulze, J.

    1981-01-01

    The fission probabilities and angular distributions of the fission fragments for the (α, α'f) reaction on 232Th and 238U at a bombarding energy of 120 MeV have been measured from about 4 to 14 MeV excitation energy. Evidence for sub-barrier resonances has been found, the negative parity ones occurri

  12. The study of the (α, α’f) reaction at 120 MeV on 232Th and 238U (I) : Fission probabilities and angular distributions in the region of the giant quadrupole resonances

    NARCIS (Netherlands)

    Plicht, J. van der; Harakeh, M.N.; van der Woude, Adriaan; David, P.; Debrus, J.; Janszen, H.; Schulze, J.

    1980-01-01

    The fission decay channel of 232Th and 238U has been investigated, using the (α, α’f) reaction at 120 MeV bombarding energy. The angular distributions of the fission fragments and the fission probabilities up to around 15 MeV excitation have been measured. No evidence for the fission decay of the gi

  13. 234U/238U Disequilibrium along stylolitic discontinuities in deep Mesozoic limestone formations of the Eastern Paris basin: evidence for discrete uranium mobility over the last 1–2 million years

    Directory of Open Access Journals (Sweden)

    P. Deschamps

    2004-01-01

    Full Text Available The (234U/238 equilibrium state of borehole core samples from the deep, low-permeability limestone formations surrounding the target argilite layer of the Meuse/Haute-Marne experimental site of the French agency for nuclear waste management -ANDRA- (Agence nationale pour la gestion des déchets radioactifs was examined to improve understanding of naturally occurring radionuclide behaviour in such geological settings. Highly precise, accurate MC-ICP-MS measurements of the (234U/238U activity ratio show that limestone samples characterised by pressure dissolution structures (stylolites or dissolution seams display systematic (234U/238U disequilibria, while the pristine carbonate samples remain in the secular equilibrium state. The systematic feature is observed throughout the zones marked by pressure dissolution structures: (i the material within the seams shows a deficit of 234U over 238U ((234U/238U down to 0.80 and (ii the surrounding carbonate matrix is characterised by an activity ratio greater than unity (up to 1.05. These results highlight a centimetric-scale uranium remobilisation in the limestone formations along these sub-horizontal seams. Although their nature and modalities are not fully understood, the driving processes responsible for these disequilibria were active during the last 1–2 Ma. Keywords: uranium isotopes, multiple-collector ICP-MS, waste management, remobilisation, migration

  14. 234U/238U Disequilibrium along stylolitic discontinuities in deep Mesozoic limestone formations of the Eastern Paris basin: evidence for discrete uranium mobility over the last 1-2 million years

    Science.gov (United States)

    Deschamps, P.; Hillaire-Marcel, C. E.; Michelot, J.-L.; Doucelance, R.; Ghaleb, B.; Buschaert, S.

    The (234U/238) equilibrium state of borehole core samples from the deep, low-permeability limestone formations surrounding the target argilite layer of the Meuse/Haute-Marne experimental site of the French agency for nuclear waste management -ANDRA- (Agence nationale pour la gestion des déchets radioactifs) was examined to improve understanding of naturally occurring radionuclide behaviour in such geological settings. Highly precise, accurate MC-ICP-MS measurements of the (234U/238U) activity ratio show that limestone samples characterised by pressure dissolution structures (stylolites or dissolution seams) display systematic (234U/238U) disequilibria, while the pristine carbonate samples remain in the secular equilibrium state. The systematic feature is observed throughout the zones marked by pressure dissolution structures: (i) the material within the seams shows a deficit of 234U over 238U ((234U/238U) down to 0.80) and (ii) the surrounding carbonate matrix is characterised by an activity ratio greater than unity (up to 1.05). These results highlight a centimetric-scale uranium remobilisation in the limestone formations along these sub-horizontal seams. Although their nature and modalities are not fully understood, the driving processes responsible for these disequilibria were active during the last 1-2 Ma.

  15. Transfer Rates of 238U and 232Th for E. globulus, A. mearnsii, H. filipendula and Hazardous Effects of the Usage of Medicinal Plants From Around Gold Mine Dump Environs

    Science.gov (United States)

    Tshivhase, Victor M.; Njinga, Raymond L.; Mathuthu, Manny; Dlamini, Thulani C.

    2015-01-01

    Medicinal plant consumption can be a source of human exposure to radioactive elements such as 238U and 232Th, which can lead to internal radiation doses. The uptake of 238U and 232Th from soils to the leaf samples of three different medicinal plant species (Eucalyptus globulus, Acacia mearnsii and Hyparrhenia filipendula) from the purlieu of the Princess gold mine dump, an abandoned contaminated tailings storage site (TSS), located at longitude 27°55′00″E and latitude 26°09′30″S in Davidsonville (Roodepoort, west of Johannesburg, South Africa) was measured. This was done using ICP-MS spectrometry and substantial differences were observed in the soil-plant transfer factor (TF) values between these radionuclides. The plant species E. globulus exhibited the highest uptake of 238U, with an average TF of 3.97, while that of H. filipendula was 0.01 and the lowest TF of 0.15 × 10−2 was measured for A. mearnsii. However, in the case of 232Th, the highest average TF was observed for A. mearnsii (0.29), followed by E. globulus (0.10) and lowest was measured for H. filipendula (0.27 × 10−2). The ratio of TF average value i.e., 238U to 232Th in the soil-plant leaves was 38.05 for E. globulus, 0.01 for A. mearnsii and 4.38 for H. filipendula. PMID:26690462

  16. The study of the (α, α’f) reaction at 120 MeV on 232Th and 238U (I) : Fission probabilities and angular distributions in the region of the giant quadrupole resonances

    NARCIS (Netherlands)

    Plicht, J. van der; Harakeh, M.N.; van der Woude, Adriaan; David, P.; Debrus, J.; Janszen, H.; Schulze, J.

    1980-01-01

    The fission decay channel of 232Th and 238U has been investigated, using the (α, α’f) reaction at 120 MeV bombarding energy. The angular distributions of the fission fragments and the fission probabilities up to around 15 MeV excitation have been measured. No evidence for the fission decay of the

  17. Distinct 238U/235U ratios and REE patterns in plutonic and volcanic angrites: Geochronologic implications and evidence for U isotope fractionation during magmatic processes

    Science.gov (United States)

    Tissot, François L. H.; Dauphas, Nicolas; Grove, Timothy L.

    2017-09-01

    Angrites are differentiated meteorites that formed between 4 and 11 Myr after Solar System formation, when several short-lived nuclides (e.g., 26Al-26Mg, 53Mn-53Cr, 182Hf-182W) were still alive. As such, angrites are prime anchors to tie the relative chronology inferred from these short-lived radionuclides to the absolute Pb-Pb clock. The discovery of variable U isotopic composition (at the sub-permil level) calls for a revision of Pb-Pb ages calculated using an ;assumed; constant 238U/235U ratio (i.e., Pb-Pb ages published before 2009-2010). In this paper, we report high-precision U isotope measurement for six angrite samples (NWA 4590, NWA 4801, NWA 6291, Angra dos Reis, D'Orbigny, and Sahara 99555) using multi-collector inductively coupled plasma mass-spectrometry and the IRMM-3636 U double-spike. The age corrections range from -0.17 to -1.20 Myr depending on the samples. After correction, concordance between the revised Pb-Pb and Hf-W and Mn-Cr ages of plutonic and quenched angrites is good, and the initial (53Mn/55Mn)0 ratio in the Early Solar System (ESS) is recalculated as being (7 ± 1) × 10-6 at the formation of the Solar System (the error bar incorporates uncertainty in the absolute age of Calcium, Aluminum-rich inclusions - CAIs). An uncertainty remains as to whether the Al-Mg and Pb-Pb systems agree in large part due to uncertainties in the Pb-Pb age of CAIs. A systematic difference is found in the U isotopic compositions of quenched and plutonic angrites of +0.17‰. A difference is also found between the rare earth element (REE) patterns of these two angrite subgroups. The δ238U values are consistent with fractionation during magmatic evolution of the angrite parent melt. Stable U isotope fractionation due to a change in the coordination environment of U during incorporation into pyroxene could be responsible for such a fractionation. In this context, Pb-Pb ages derived from pyroxenes fraction should be corrected using the U isotope composition

  18. Chemical fertilizers as a source of (238)U, (40)K, (226)Ra, (222)Rn, and trace metal pollutant of the environment in Saudi Arabia.

    Science.gov (United States)

    Alshahri, Fatimh; Alqahtani, Muna

    2015-06-01

    The specific activities of (238)U, (226)Ra, (40)K, and (222)Rn in chemical fertilizers were measured using gamma ray spectrometer and Cr-39 detector. In this study, 21 chemical fertilizers were collected from Eastern Saudi Arabian markets. The specific activities of (238)U ranged from 23 ± 0.5 to 3900 ± 195 Bq kg(-1); (226)Ra ranged from 5.60 ± 2.80 to 392 ± 18 Bq kg(-1); and (40)K ranged from 18.4 ± 3 to 16,476 ± 820 Bq kg(-1). The radon concentrations and the radon exhalation rates were found to vary from 3.20 ± 1.20 to 1532 ± 160 Bq m(-3) and from 1.60 to 774 mBq m(-2) h(-1), respectively. Radium equivalent activities (Raeq) were calculated for the analyzed samples to assess the radiation hazards arising due to the use of these chemical fertilizers in the agriculture soil. The Raeq for six local samples (nitrogen, phosphorous, and potassium (NPK) and single superphosphate (SSP)) and one imported sample (Sulfate of Potash (SOP)) were greater than the acceptable value 370 Bq kg(-1). The total air absorbed doses rates in air 1 m above the ground (D) were calculated for all samples. All samples, except one imported granule sample diammonium phosphate (DAP), were higher than the estimated average global terrestrial radiation of 55 nGy h(-1). The highest annual effective dose was in triple super phosphate (TSP) fertilizers (2.1 mSv y(-1)). The results show that the local TSP, imported SOP, and local NPK (sample 13) fertilizers were unacceptable for use as fertilizers in agricultural soil. Furthermore, the toxic elements and trace metals (Pb, Cd, Cr, Co, Ni, Hg, and As) were determined using atomic absorption spectrometer. The concentrations of chromium in chemical fertilizers were higher than the global values.

  19. 贫化铀球装置内的238U(n,2n)反应率实验研究%Measurement of 238 U(n,2n) Reaction Rate in Depleted Uranium Sphere

    Institute of Scientific and Technical Information of China (English)

    朱传新; 牟云峰; 郑普; 王新华; 郭海萍; 何铁

    2015-01-01

    采用两套不同尺寸的贫化铀球装置开展了装置内部的238 U (n ,2n)反应率实验研究,利用PD‐300加速器D‐T中子源辐照实验装置,源强变化采用伴随粒子法监测,238 U圆片放置在实验装置的45°孔道内,分布在距中子源不同距离处,辐照结束后,采用 HPGe探测器测量238 U圆片活化γ射线。实验结果与蒙特卡罗程序模拟计算结果进行了比较和分析。结果表明,238 U (n ,2n)反应率实验结果与模拟计算值较吻合,238 U (n ,2n)反应率随球体半径 r的增加,近似服从e- ar/r2分布规律。%The 238 U (n ,2n) reaction rates of two depleted uranium spheres were meas‐ured .The depleted uranium spheres were irradiated by D‐T neutron at PD‐300 accelera‐tor .The intensity of neutron source was monitored by the associated‐alpha particles from the T (d ,n)He reaction .After radiation ,the activated gamma rays of uranium foils in the 45° hole of uranium spheres were measured using HPGe detector .The 238 U(n ,2n) reaction rates of two depleted uranium spheres were calculated using Monte‐Carlo simu‐lation .It shows that the 238 U(n ,2n) reaction rates from experiments are agreed with the calculations .The change of 238 U(n ,2n) reaction rate with the radius r of depleted urani‐um sphere is obeyed approximately the distribution of e - ar/r2 .

  20. Determination of extremely low {sup 236}U/{sup 238}U isotope ratios in environmental samples by sector-field inductively coupled plasma mass spectrometry using high-efficiency sample introduction

    Energy Technology Data Exchange (ETDEWEB)

    Boulyga, Sergei F. [Institute of Inorganic Chemistry and Analytical Chemistry, Johannes Gutenberg-University Mainz, Duesbergweg 10-14, 55099 Mainz (Germany)]. E-mail: sergei.boulyga@univie.ac.at; Heumann, Klaus G. [Institute of Inorganic Chemistry and Analytical Chemistry, Johannes Gutenberg-University Mainz, Duesbergweg 10-14, 55099 Mainz (Germany)

    2006-07-01

    A method by inductively coupled plasma mass spectrometry (Icp-Ms) was developed which allows the measurement of {sup 236}U at concentration ranges down to 3 x 10{sup -14} g g{sup -1} and extremely low {sup 236}U/{sup 238}U isotope ratios in soil samples of 10{sup -7}. By using the high-efficiency solution introduction system APEX in connection with a sector-field ICP-MS a sensitivity of more than 5000 counts fg{sup -1} uranium was achieved. The use of an aerosol desolvating unit reduced the formation rate of uranium hydride ions UH{sup +}/U{sup +} down to a level of 10{sup -6}. An abundance sensitivity of 3 x 10{sup -7} was observed for {sup 236}U/{sup 238}U isotope ratio measurements at mass resolution 4000. The detection limit for {sup 236}U and the lowest detectable {sup 236}U/{sup 238}U isotope ratio were improved by more than two orders of magnitude compared with corresponding values by alpha spectrometry. Determination of uranium in soil samples collected in the vicinity of Chernobyl nuclear power plant (NPP) resulted in that the {sup 236}U/{sup 238}U isotope ratio is a much more sensitive and accurate marker for environmental contamination by spent uranium in comparison to the {sup 235}U/{sup 238}U isotope ratio. The ICP-MS technique allowed for the first time detection of irradiated uranium in soil samples even at distances more than 200 km to the north of Chernobyl NPP (Mogilev region). The concentration of {sup 236}U in the upper 0-10 cm soil layers varied from 2 x 10{sup -9} g g{sup -1} within radioactive spots close to the Chernobyl NPP to 3 x 10{sup -13} g g{sup -1} on a sampling site located by >200 km from Chernobyl.

  1. New prompt fission neutron spectra measurements in the 238U(n,f) reaction with a dedicated setup at LANSCE/WNR

    Science.gov (United States)

    Laurent, Benoit; Marini, Paola; Bélier, Gilbert; Bonnet, Thomas; Chatillon, Audrey; Taieb, Julien; Etasse, David; Devlin, Matthew; Haight, Robert

    2017-09-01

    A new prompt fission neutron spectra (PFNS) measurement in the 238U(n,f) reaction was performed at LANSCE/WNR facility. Evaluated data show discrepancies on the low (below 1 MeV) and high (above 5 MeV) energy parts in the PFNS for different major and minor actinides. The goal is to improve these measurements in a wide range of incident energy. The energy of the incoming neutron, inducing the fission, and the prompt neutron energies, are measured by time-of-flight method. A dedicated fission chamber was developed, in order to improve alpha-fission discrimination, timing resolution, actinide mass, and to reduce the amount of neutron scattering. To detect prompt neutrons, the 54 Chi-Nu scintillator cells array were surrounding the fission chamber. High statistics were recorded during this experiment, allowing a precise study of PFNS behavior as a function of incident neutron energy, from 1 MeV to 200 MeV. This experiment also showed that all the new tools developed to improve PFNS measurements are performing. Therefore, measurements of PFNS with others actinides such as 239Pu are planned.

  2. Vertical and horizontal distribution of radionuclides (232Th, 238U and 40K) in sediment from Manjung coastal water area Perak, Malaysia

    Science.gov (United States)

    Abdullah, Anisa; Hamzah, Zaini; Saat, Ahmad; Wood, Ab. Khalik

    2016-01-01

    Distribution of radionuclides from anthropogenic activities has been widely studied in marine coastal area. Due to rapid population growth and socio-economic development in Manjung area such as coal fired power plant, iron foundries, port development, waste discharged from factories and agriculture runoff may contribute to increase in pollution rate. The radioactive materials from anthropogenic activities could deteriorate the quality of the marine ecosystem and thus lead to possible radiological health risk to the population. Radionuclides (232Th, 238U and 40K) content in surface and profile sediment from Manjung coastal area was determined in this study. Radionuclides in sediment from seven locations were collected using sediment core sampling and measurements were carried out using Energy Dispersive X-ray Fluorescence (EDXRF) spectroscopy. The results show that the concentration of radionuclides in surface sediment and distribution trend of depth vertical profile sediment generally varies depending on locations. Enrichment factors (EF), geo-accumulation index (Igeo) and pollution index (PI) were applied to determine level of pollution of this study area. The radiological risks related to human exposure were evaluated based on external hazard index (Hex).

  3. Capture and Fission rate of 232-Th, 238-U, 237-Np and 239-Pu from spallation neutrons in a huge block of lead.

    CERN Document Server

    Vlachoudis, Vasilis

    2000-01-01

    The study is centered on the research of the incineration possibility of nuclear waste, by the association of a particle accelerator with a multiplying medium of neutrons, in the project "Energy Amplifier" of C. Rubbia. It consists of the experimental determination of the rates of capture and fission of certain elements (232-Th, 238-U, 237-Np and 239-Pu) subjected to a fluence of fast spallation neutrons. These neutrons are produced by the interaction of high kinetic energy protons (several GeV) provided by the CERN-PS accelerator, on a large lead solid volume. The measurement techniques used in this work, are based on the activation of elements in the lead volume and the subsequent gamma spectroscopy of the activated elements, and also by the detection of fission fragment traces. The development, of a Monte Carlo code makes it possible, on one hand, to better understand the relevant processes, and on the other hand, to validate the code, by comparison with measurements, for the design and the construction of...

  4. Observation of new neutron-rich micro-second isomers among fission products of ^238U at 345 MeV/u

    Science.gov (United States)

    Kameda, Daisuke; Nakao, Taro; Kubo, Toshiyuki; Ohnishi, Tetsuya; Takeda, Hiroyuki; Fukuda, Naoki; Kusaka, Kensuke; Yoshida, Atsushi; Yoshida, Koichi; Ohtake, Masao; Inabe, Naohito; Yanagisawa, Yoshiyuki; Tanaka, Kanenobu; Gono, Yasuyuki

    2009-10-01

    In the production of the radioactive isotope (RI) beam using projectile fragment separators, γ rays emitted from metastable states, isomers, of the reaction products can be used as a fingerprint of the isotope that is analyzed in the separator. In the operation of the superconducting in-flight RI beam separator BigRIPS [1] at RIKEN RI Beam Factory, the detection of such γ rays plays important roles not only in the identification of the RI beam [2] but also in searching for new isomers, providing valuable spectroscopic information on the isotopes. In the recent new-isotope production experiment with BigRIPS using in-flight fission of 345 MeV/nucleon ^238U at the beam intensity around 0.3 pnA, we have observed a number of short-lived isomeric decays which include unknown decays from more than 10 isotopes, using three clover-type Ge detectors with a beam stopper of aluminum. The primal result of the observations will be reported. [1] T. Kubo: Nucl. Instr. and Meth. B 204 (2003) 97. [2] T. Ohnishi et al.: J. Phys. Soc. Japan, 77 (2008) 083201.

  5. Vertical and horizontal distribution of radionuclides ({sup 232}Th, {sup 238}U and {sup 40}K) in sediment from Manjung coastal water area Perak, Malaysia

    Energy Technology Data Exchange (ETDEWEB)

    Abdullah, Anisa, E-mail: coppering@ymail.com; Hamzah, Zaini; Wood, Ab. Khalik [Faculty of Applied Sciences, Universiti Teknologi MARA, 40450, Shah Alam, Selangor (Malaysia); Saat, Ahmad [Faculty of Applied Sciences, Universiti Teknologi MARA, 40450, Shah Alam, Selangor (Malaysia); Institute of Science, Universiti Teknologi MARA, 40450 Shah Alam, Selangor (Malaysia)

    2016-01-22

    Distribution of radionuclides from anthropogenic activities has been widely studied in marine coastal area. Due to rapid population growth and socio-economic development in Manjung area such as coal fired power plant, iron foundries, port development, waste discharged from factories and agriculture runoff may contribute to increase in pollution rate. The radioactive materials from anthropogenic activities could deteriorate the quality of the marine ecosystem and thus lead to possible radiological health risk to the population. Radionuclides ({sup 232}Th, {sup 238}U and {sup 40}K) content in surface and profile sediment from Manjung coastal area was determined in this study. Radionuclides in sediment from seven locations were collected using sediment core sampling and measurements were carried out using Energy Dispersive X-ray Fluorescence (EDXRF) spectroscopy. The results show that the concentration of radionuclides in surface sediment and distribution trend of depth vertical profile sediment generally varies depending on locations. Enrichment factors (EF), geo-accumulation index (I{sub geo}) and pollution index (PI) were applied to determine level of pollution of this study area. The radiological risks related to human exposure were evaluated based on external hazard index (H{sub ex})

  6. Determination of Fission Product Yields of 235U, 238U and 239Pu for Neutron Energies from 0.5 to 14.8 MeV

    Science.gov (United States)

    Gooden, Matthew; Arnold, Charles; Becker, John; Bhatia, Chitra; Bhike, Megha; Fowler, Malcolm; Howell, Calvin; Kelley, John; Stoyer, Mark; Tonchev, Anton; Tornow, Werner; Vieira, Dave; Wilhelmy, Jerry

    2014-03-01

    A joint TUNL-LANL-LLNL collaboration has been formed to study the issue of possible energy dependences for certain fission product isotopes. Work has been carried out at the TUNL 10 MV Tandem accelerator which produces nearly mono-energetic neutrons via either 2H(d,n)3He,3H(d,n)4He,or3H(p,n)3He reactions. Three dual fission ionization chambers dedicated to 235U, 238U and 239Pu thick target foils and thin monitor foils respectively, were exposed to the neutron beams. After irradiation, thick target foils were gamma counted over a period of 1-2 months and characteristic gamma rays from fission products were recorded using HPGe detectors at TUNL's low background counting area. Using the dual fission chambers, relative fission product yield were determined at a high precision of 2-3 % as well as absolute fission product yields at a lower precision of 5-6 %. Preliminary results will be presented for a number of fission product isotopes over the incident neutron energy range of 0.5 to 14.8 MeV.

  7. Energy Dependence of Neutron-Induced Fission Product Yields of 235U, 238U and 239Pu Between 0.5 and 14.8 MeV

    Science.gov (United States)

    Gooden, Matthew; Tornow, Werner; Tonchev, Anton; Vieira, Dave; Wilhelmy, Jerry; Arnold, Charles; Fowler, Malcolm; Stoyer, Mark

    2014-09-01

    Under a joint collaboration between TUNL-LANL-LLNL, a set of absolute fission product yield measurements have been performed. The energy dependence of a number of cumulative fission products between 0.5 and 14.8 MeV have been measured using quasi-monoenergetic neutron beams for three actinide targets, 235U, 238U and 239Pu, between 0.5 and 14.8 MeV. The FPYs were measured by a combination of activation utilizing specially designed dual-fission chambers and γ-ray counting. The dual-fission chambers are back-to-back ionization chambers encasing a target with thin deposits of the same target isotope in each chamber. This method allows for the direct measurement of the fission rate in the activation target with no reference to the fission cross-section, reducing uncertainties. γ-ray counting was performed on well-shield HPGe detectors over a period of 2 months per activation to properly identify fission products. Reported are absolute cumulative fission product yields for incident neutron energies of 0.5, 1.37, 2.4, 4.6 and 14.8 MeV.

  8. On an Increase of Critical Current in High Temperature Superconductors Doped with $^{238}U$ Due to the Production of Nuclear Photofission Fragment Tracks

    CERN Document Server

    Goncharov, I N

    2001-01-01

    The effect of appreciable increasing J_c(B,T) in HTSC (especially at liquid nitrogen temperatures of 62-78 K and magnetic fields of above 0.5 T) due to the production of fast heavy ion tracks, including those of doped U nuclear fission fragments, is known. The tracks are additional effective pinning-centers. The results described in the literature have been obtained for {235}U doped HTSC after reactor thermal neutron irradiations. Disadvantages of such a method are analyzed in this paper, in particular in case of its use for current-carrying Bi-2223/Ag tape, because a very high radioactivity level slowly decreasing in time arises. The author has suggested to use {238}U nuclear photofission in over a giant resonance energy range (E_gamma ~10-20 MeV). The experimental results obtained after tape irradiation with gamma-quanta (E_gamma \\leq 24 MeV), including a time dependence of radioactivity level, are presented. Possibilities of practical realization of this method are discussed.

  9. {sup 230}Th, {sup 232}Th and {sup 238}U determinations in phosphoric acid fertilizer and process products by ICP-MS

    Energy Technology Data Exchange (ETDEWEB)

    Nascimento, Marcos R.L. do; Guerreiro, Luisa M.R.; Bonifacio, Rodrigo L.; Taddei, Maria H.T., E-mail: pmarcos@cnen.gov.br [Comissao Nacional de Energia Nuclear (LAPOC/CNEN-MG), Pocos de Caldas, MG (Brazil). Laboratorio de Pocos de Caldas

    2015-07-01

    Through processing of Santa Quiteria-CE mine phosphate rock, Brazil has established a project for production of phosphoric acid fertilizer and uranium as a by-product. Under leaching conditions of phosphate rock with sulfuric acid, which is the common route for preparing phosphoric acid fertilizer, a large part of uranium, thorium and their decay products naturally present in the rock are solubilized. In order to assess the contamination potential in phosphoric acid and others process products, this paper describes a previous precipitation and direct methods for routine analysis of thorium and uranium isotopes by ICP-MS. In all samples, {sup 230}Th, {sup 232}Th and {sup 238}U were directly determined after dilution, except {sup 230}Th in phosphoric acid loaded with uranium sample, which to overcome equipment contamination effect, was determined after its separation by oxalate precipitation using lanthanum as a carrier. The results obtained by the proposed method by ICP-MS, were in good agreement when compared to alpha spectrometry for {sup 230}Th, and ICP-OES and spectrophotometry with arsenazo III for elementary uranium and thorium determinations. (author)

  10. Temporal evolution of natural radionuclides distributions {sup 238}U, {sup 234}Th, {sup 226}Ra, {sup 228}Ra, {sup 210}Pb and {sup 210}Po in the Bransfield strait, Antarctica peninsula; Evolucao temporal das distribuicoes dos radionuclideos naturais {sup 238}U, {sup 234}Th, {sup 226}Ra, {sup 228}Ra, {sup 210}Pb and {sup 210}Po no estreito de Bransfiel, peninsula Antartica

    Energy Technology Data Exchange (ETDEWEB)

    Lapa, Flavia Valverde

    2013-07-01

    Research on the distribution of natural radionuclides in Antarctica is rare and thus, there is great interest in to know their occurrence and factors related to its mobilization, transference and accumulation in this extremely fragile environment. Natural radionuclides have been used intensively as tracers in the ocean, helping to better understand processes as sinking and particle resuspension, water masses mixture and oceanic circulation. {sup 234}Th (t½ = 24.1 days) is a particle-reactive radionuclide produced continuously in seawater by the decay of its soluble precursor conservative with salinity {sup 238}U (t½ = 4.5 10{sup 9} years). Since {sup 234}Th presents relatively short half-life, it is used to quantify processes that occur in temporal scale varying from days to weeks. The disequilibrium {sup 234}Th/{sup 238}U in the surface ocean has been applied to estimate carbon fluxes exported via sinking material. The flux of particles biologically productive out of the euphotic zone in the Southern Ocean has special attention due to its importance in the control of CO{sub 2} atmospheric concentrations. The radionuclides {sup 210}Pb (t½ = 22.3 years) and {sup 210}Po (t½ = 138 days) are also particle-reactive. The disequilibrium {sup 210}Po/{sup 210}Pb has been used to estimate fluxes of particles exported in the ocean in the time scale of weeks. The long-lived Ra isotopes, {sup 226}Ra (t½ = 1,600 years) and {sup 228}Ra (t½ = 5.75 years) are soluble in seawater, presenting unique properties that make them excellent tracers of water masses. This research work had the aim to study the distributions of natural radionuclides {sup 238}U, {sup 234}Th, {sup 22}'6Ra, {sup 22}'8Ra, {sup 210}Pb and {sup 210}Po in the Bransfield Strait during 2 samplings carried out in the 2011 Austral Summer (OPERANTAR XXIX and XXX). (author)

  11. Determination of 238 U,226 Ra and the Calculation of Equilibrium Coefficient in Rock of Gangdise Tectonic Belt,Tibet%西藏冈底斯构造带岩(矿)石中238U 、226Ra测定及铀镭平衡系数计算

    Institute of Scientific and Technical Information of China (English)

    齐玲

    2015-01-01

    通过对西藏冈底斯构造带岩矿石中铀、镭测定结果的初步研究发现,铀矿(化)体中铀、镭平衡系数趋于1,而区内铀含量较低的水系沉积物、花岗岩、酸性火山岩等显示较强的偏镭特征。%The Gangdise tectonic belt is an important part of the Tethyan tectonic domain ,preliminary study on the dctermination result of 238 U and 226 Ra in the rocks and ores from the belt found that equilib‐rium coefficient of the uranium‐radium tends to 1 in uranium mineralized bodies , but low uranium content rock of river sediments , granite and acid volcanic is characterized by rich radium .

  12. The Role of Plants in the 238U-234U Disequilibria of Stream Waters: The Example of the Strengbach Watershed (Vosges, France)

    Science.gov (United States)

    Pierret, M.; Chbaaux, F.

    2004-12-01

    Recent TIMS or MC ICPMS analyses of U disequilibria in the dissolved load of stream and river waters have confirmed the potential of the U activity ratio in river waters as a specific tracer of chemical fluxes coming from rocks and soils (e.g., 1). These precise measurements have also outlined that occurrence of U activity ratios lower than one in dissolved load of river waters is not exceptional, especially at the scale of small watersheds. Such U values pose in turn the question of the real mechanisms controlling the supply of 234U-238U isotopes to the freshwaters. In order to address this question U activity ratios, Sr isotope ratios and the concentrations of major and some trace elements were analyzed in the different compartments of a small granitic watershed: the Strengbach environmental observatory (Vosges, France) ( http://ohge.u-strasbg.fr). In addition of the different streamwaters draining this watershed, the main horizons of weathering profiles, the associated soil solutions and the main tree species growing around were analyzed. The data confirm that the Strengbach stream water samples have generally U activity ratios lower than one and point out that soils solutions display a similar range of U and Sr variations. By contrast, tree and plant samples define different trends of variation in a plot of U activity ratios against Sr isotope ratios with, above all, U activity ratios systematically greater than one. These data show that trees and plants collected during this work cannot directly pomp their nutriments from soils and soil solutions sampled here, i.e. gravity solutions. They also suggest that, in this watershed, the plants, especially trees, play a central role in the weathering processes of rocks and minerals, and control a large part of the geochemical signature of the water samples collected on this watershed, including their U activity ratios. 1Riotte J and Chabaux F. (1999) GCA 63, 1263-1275.

  13. Energy dependence of fission product yields from 235U, 238U, and 239Pu with monoenergetic neutrons between thermal and 14.8 MeV

    Science.gov (United States)

    Gooden, Matthew; Arnold, Charles; Bhike, Megha; Bredeweg, Todd; Fowler, Malcolm; Krishichayan; Tonchev, Anton; Tornow, Werner; Stoyer, Mark; Vieira, David; Wilhelmy, Jerry

    2017-09-01

    Under a joint collaboration between TUNL-LANL-LLNL, a set of absolute fission product yield measurements has been performed. The energy dependence of a number of cumulative fission product yields (FPY) have been measured using quasi-monoenergetic neutron beams for three actinide targets, 235U, 238U and 239Pu, between 0.5 and 14.8 MeV. The FPYs were measured by a combination of fission counting using specially designed dual-fission chambers and γ-ray counting. Each dual-fission chamber is a back-to-back ionization chamber encasing an activation target in the center with thin deposits of the same target isotope in each chamber. This method allows for the direct measurement of the total number of fissions in the activation target with no reference to the fission cross-section, thus reducing uncertainties. γ-ray counting of the activation target was performed on well-shielded HPGe detectors over a period of two months post irradiation to properly identify fission products. Reported are absolute cumulative fission product yields for incident neutron energies of 0.5, 1.37, 2.4, 3.6, 4.6, 5.5, 7.5, 8.9 and 14.8 MeV. Preliminary results from thermal irradiations at the MIT research reactor will also be presented and compared to present data and evaluations. This work was performed under the auspices of the U.S. Department of Energy by Los Alamos National Security, LLC under contract DE-AC52-06NA25396, Lawrence Livermore National Laboratory under contract DE-AC52-07NA27344 and by Duke University and Triangle Universities Nuclear Laboratory through NNSA Stewardship Science Academic Alliance grant No. DE-FG52-09NA29465, DE-FG52-09NA29448 and Office of Nuclear Physics Grant No. DE-FG02-97ER41033.

  14. Extensive radioactive characterization of a phosphogypsum stack in SW Spain: {sup 226}Ra, {sup 238}U, {sup 210}Po concentrations and {sup 222}Rn exhalation rate

    Energy Technology Data Exchange (ETDEWEB)

    Abril, Jose-Maria, E-mail: jmabril@us.es [Dpto. Fisica Aplicada I, Universidad de Sevilla, EUITA, Ctra Utrera Km 1, 41013 Seville (Spain); Garcia-Tenorio, Rafael, E-mail: gtenorio@us.es [Dpto. Fisica Aplicada II, Universidad de Sevilla, ETSA, Avda. Reina Mercedes s/n, 41012 Seville (Spain); Manjon, Guillermo, E-mail: manjon@us.es [Dpto. Fisica Aplicada II, Universidad de Sevilla, ETSA, Avda. Reina Mercedes s/n, 41012 Seville (Spain)

    2009-05-30

    Phosphogypsum (PG) is a by-product of the phosphate fertilizer industries that contains relatively high concentrations of uranium series radionuclides. The US-EPA regulates the agriculture use of PG, attending to its {sup 226}Ra content and to the {sup 222}Rn exhalation rate from inactive stacks. Measurements of {sup 222}Rn exhalation rates in PG stacks typically show a large and still poorly understood spatial and temporal variability, and the published data are scarce. This work studies an inactive PG stack in SW Spain of about 0.5 km{sup 2} from where PG can be extracted for agriculture uses, and an agriculture soil 75 km apart, being representative of the farms to be amended with PG. Activity concentrations of {sup 226}Ra, {sup 238}U and {sup 210}Po have been measured in 30 PG samples (0-90 cm horizon) allowing for the construction of maps with spatial distributions in the PG stack and for the characterization of the associated PG inputs to agriculture soils. Averaged {sup 226}Ra concentrations for the stack were 730 {+-} 60 Bq kg{sup -1} (d.w.), over the US-EPA limit of 370 Bq kg{sup -1}. {sup 222}Rn exhalation rate has been measured by the charcoal canister method in 49 sampling points with 3 canisters per sampling point. Values in PG stack were under the US-EPA limit of 2600 Bq m{sup -2} h{sup -1}, but they were one order of magnitude higher than those found in the agriculture soil. Variability in radon emissions has been studied at different spatial scales. Radon exhalation rates were correlated with {sup 226}Ra concentrations and daily potential evapotranspiration (ETo). They increased with ETo in agriculture soils, but showed an opposite behaviour in the PG stack.

  15. Extensive radioactive characterization of a phosphogypsum stack in SW Spain: 226Ra, 238U, 210Po concentrations and 222Rn exhalation rate.

    Science.gov (United States)

    Abril, José-María; García-Tenorio, Rafael; Manjón, Guillermo

    2009-05-30

    Phosphogypsum (PG) is a by-product of the phosphate fertilizer industries that contains relatively high concentrations of uranium series radionuclides. The US-EPA regulates the agriculture use of PG, attending to its (226)Ra content and to the (222)Rn exhalation rate from inactive stacks. Measurements of (222)Rn exhalation rates in PG stacks typically show a large and still poorly understood spatial and temporal variability, and the published data are scarce. This work studies an inactive PG stack in SW Spain of about 0.5 km(2) from where PG can be extracted for agriculture uses, and an agriculture soil 75 km apart, being representative of the farms to be amended with PG. Activity concentrations of (226)Ra, (238)U and (210)Po have been measured in 30 PG samples (0-90 cm horizon) allowing for the construction of maps with spatial distributions in the PG stack and for the characterization of the associated PG inputs to agriculture soils. Averaged (226)Ra concentrations for the stack were 730+/-60 Bq kg(-1) (d.w.), over the US-EPA limit of 370 Bq kg(-1). (222)Rn exhalation rate has been measured by the charcoal canister method in 49 sampling points with 3 canisters per sampling point. Values in PG stack were under the US-EPA limit of 2600 Bq m(-2)h(-1), but they were one order of magnitude higher than those found in the agriculture soil. Variability in radon emissions has been studied at different spatial scales. Radon exhalation rates were correlated with (226)Ra concentrations and daily potential evapotranspiration (ETo). They increased with ETo in agriculture soils, but showed an opposite behaviour in the PG stack.

  16. Standard practice for the determination of 237Np, 232Th, 235U and 238U in urine by inductively coupled plasma-Mass spectrometry (ICP-MS) and gamma ray spectrometry.

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2005-01-01

    1.1 This practice covers the separation and preconcentration of neptunium-237 (237Np), thorium-232 (232Th), uranium-235 (235U) and uranium-238 (238U) from urine followed by quantitation using ICP-MS. 1.2 This practice can be used to support routine bioassay programs. The minimum detectable concentrations (MDC) for this method, taking the preconcentration factor into account, are approximately 1E-2Bq for 237Np (0.38ng), 2E-6Bq for 232Th (0.50ng), 4E-5Bq for 235U (0.50ng) and 6E-6Bq for 238U (0.48ng). 1.3 This standard does not purport to address all of the safety problems, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

  17. Measurement of 238U and 232Th in Petrol, Gas-oil and Lubricant Samples by Using Nuclear Track Detectors and Resulting Radiation Doses to the Skin of Mechanic Workers.

    Science.gov (United States)

    Misdaq, M A; Chaouqi, A; Ouguidi, J; Touti, R; Mortassim, A

    2015-10-01

    Workers in repair shops of vehicles (cars, buses, truck, etc.) clean carburetors, check fuel distribution, and perform oil changes and greasing. To explore the exposure pathway of (238)U and (232)Th and its decay products to the skin of mechanic workers, these radionuclides were measured inside petrol, gas-oil, and lubricant material samples by means of CR-39 and LR-115 type II solid state nuclear track detectors (SSNTDs), and corresponding annual committed equivalent doses to skin were determined. The maximum total equivalent effective dose to skin due to the (238)U and (232)Th series from the application of different petrol, gas-oil, and lubricant samples by mechanic workers was found equal to 1.2 mSv y(-1) cm(-2).

  18. Seasonal and spatial variability of {sup 210}Po, {sup 238}U and {sup 239+240}Pu levels in the river catchment area assessed by application of neural-network based classification

    Energy Technology Data Exchange (ETDEWEB)

    Skwarzec, Bogdan [University of Gdansk, Faculty of Chemistry, Chair of Analytical Chemistry, 18/19 Sobieskiego Street, 80-952 Gdansk (Poland)], E-mail: bosk@chem.univ.gda.pl; Kabat, Krzysztof [University of Gdansk, Faculty of Chemistry, Chair of Analytical Chemistry, 18/19 Sobieskiego Street, 80-952 Gdansk (Poland); Astel, Aleksander [Pomeranian Academy, Biology and Environmental Protection Institute, Environmental Chemistry Research Unit, 22a Arciszewskiego Street, 76-200 Slupsk (Poland)

    2009-02-15

    The present study deals with the application of self-organizing maps (SOM) in order to model, classify and interpret seasonal and spatial variability of {sup 210}Po, {sup 238}U and {sup 239+240}Pu levels in the Vistula river basin. The data set represents concentration values for 3 alpha emitters ({sup 210}Po, {sup 238}U and {sup 239+240}Pu) measured in surface water samples collected at 19 different sampling locations (8 in major Vistula stream while 11 in right or left Vistula tributaries) during four seasons (winter, spring, summer and autumn) in the framework of a one-year quality monitoring study. The advantages of an SOM algorithm, its classification and visualization ability for environmental data sets, are stressed. The neural-network based classification made it possible to reveal specific patterns related to both seasonal and spatial variability. In the middle and upper part of Vistula catchment as well as in the right-shore tributaries, concentrations of {sup 210}Po and {sup 238}U during summer and winter are the lowest. Concentrations of {sup 210}Po and {sup 238}U increase significantly during spring and autumn in the Vistula river catchment, especially in the delta of Vistula river. High concentration of anthropogenic originated {sup 239+240}Pu indicates 'site-specific' character of pollution in two large left-shore tributaries located in the middle part of the Vistula drainage area. Efficient classification of sampling locations could lead to an optimization of river radiochemical sampling networks and to a better tracing of natural and anthropogenic changes along Vistula river stream.

  19. Measurement of activity concentrations of {sup 40}K, 2{sup 32T}h and {sup 238}U in TSP aerosols and the associated inhalation annual effective radiation dose to the public in Gosan site, Jeju

    Energy Technology Data Exchange (ETDEWEB)

    Han, Chung Hun; Park, Youn Hyun; Park, Jae Woo [Jeju National University, Jeju (Korea, Republic of)

    2016-10-15

    Gamma radiation emitted from naturally occurring radioisotopes, such as 40K and the radionuclides from the {sup 232}Th and {sup 238}U series and their decay products, which exist at trace levels in all ground formations, represents the main external source of irradiation to the human body. The objective of the current study is to determine the activity concentrations of 40K, {sup 232}Th and {sup 238}U in airborne TSP and the associated internal radiation dose to the public due to inhalation in Gosan site, Jeju Island, Korea. The atmospheric total suspended particulates (TSP) aerosols were collected at Gosan site of Jeju Island, which is one of the background sites of Korea, during January to April 2013. This study analyzed using ICP-DRC-MS the concentrations of potassium, uranium and thorium, and evaluated the annual effective dose by breathing from the results. The correlations between the studied natural isotopes is a good positive correlation between {sup 232}Th and {sup 238}U, supporting the conclusion that they originated from the same source, mostly the crust. The backward trajectory analysis has confirmed that the 40K, {sup 238}U and {sup 232}Th are delivered as the air masses have moved from the China continent. The inhalation annual effective radiation dose (default mode F) to the public due to natural isotopes of the airborne TSP was in the range 16.195 - 77.051 nSv/y, depending on the age group. Jeju Island with less pollution source and low population density is also one of the best places as a background area in Asia.

  20. Characterization of bauxite residue (red mud) for (235)U, (238)U, (232)Th and (40)K using neutron activation analysis and the radiation dose levels as modeled by MCNP.

    Science.gov (United States)

    Landsberger, S; Sharp, A; Wang, S; Pontikes, Y; Tkaczyk, A H

    2017-07-01

    This study employs thermal and epithermal neutron activation analysis (NAA) to quantitatively and specifically determine absorption dose rates to various body parts from uranium, thorium and potassium. Specifically, a case study of bauxite residue (red mud) from an industrial facility was used to demonstrate the feasibility of the NAA approach for radiological safety assessment, using small sample sizes to ascertain the activities of (235)U, (238)U, (232)Th and (40)K. This proof-of-concept was shown to produce reliable results and a similar approach could be used for quantitative assessment of other samples with possible radiological significance. (238)U and (232)Th were determined by epithermal and thermal neutron activation analysis, respectively. (235)U was determined based on the known isotopic ratio of (238)U/(235)U. (40)K was also determined using epithermal neutron activation analysis to measure total potassium content and then subtracting its isotopic contribution. Furthermore, the work demonstrates the application of Monte Carlo Neutral-Particle (MCNP) simulations to estimate the radiation dose from large quantities of red mud, to assure the safety of humans and the surrounding environment. Phantoms were employed to observe the dose distribution throughout the human body demonstrating radiation effects on each individual organ. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Eruption and magma crystallization ages of Las Tres Vírgenes (Baja California) constrained by combined 230Th/ 238U and (U-Th)/He dating of zircon

    Science.gov (United States)

    Schmitt, Axel K.; Stockli, Daniel F.; Hausback, Brian P.

    2006-11-01

    Las Tres Vírgenes volcano is a calc-alkaline composite cone located near the main Gulf of California escarpment on the E coast of the Baja California peninsula. High-sensitivity ion microprobe U-series ( 230Th/ 238U) ages for zircon from La Vírgen tephra average 121 - 10 + 12 ka (1σ; MSWD = 2.7), with discrete age peaks at ˜ 100 and 160 ka. The noble gas mass spectrometric (U-Th)/He zircon age, corrected for disequilibrium and pre-eruptive storage, is 36 ± 3 ka. This result for the eruption age of La Vírgen tephra is significantly older than previously postulated historic or Holocene ages that were based on an 18th century map reference and 14C dating of accidental charcoal, respectively. The new (U-Th)/He zircon age is consistent with a > 26 ± 4 ka age derived from cosmogenic He exposure dating of an overlying basaltic lava flow [Hausback, B.P. and Abrams, M.J., 1996. Plinian eruption of La Virgen Tephra, Volcán Las Tres Virgenes, Baja California Sur, Mexico. Eos, Transactions, American Geophysical Union, 77(46, Suppl.): 813-814.]. U-Pb zircon analysis of ignimbrites erupted from the adjacent Early Pleistocene La Reforma and El Aguajito calderas yielded ages of 1.38 ± 0.03 Ma ( n = 12; MSWD = 1.0) and 1.17 ± 0.07 Ma ( n = 23; MSWD = 1.3), respectively. No evidence for these ages is found among La Vírgen zircons, whereas pre-Quaternary zircon xenocrysts are common. The La Vírgen magma, therefore, evolved unrelated to Early Pleistocene magmatism in adjacent calderas, but assimilated local basement rocks. A gap between average Th-U and (U-Th)/He zircon ages suggests that zircon crystallization was discontinuous in the La Vírgen magma chamber. In addition, partial resorption of zircon suggests episodic thermal rejuvenation, most likely by basaltic recharge. Based on the zircon record, the > 100 ka lifetime of the thermal anomaly that sustained repeated intrusive pulses significantly exceeds the age of the last eruption. This strengthens the view that Tres

  2. Discriminating assimilants and decoupling deep- vs. shallow-level crystal records at Mount Adams using 238U-230Th disequilibria and Os isotopes

    Science.gov (United States)

    Jicha, B.R.; Johnson, C.M.; Hildreth, W.; Beard, B.L.; Hart, G.L.; Shirey, S.B.; Singer, B.S.

    2009-01-01

    A suite of 23 basaltic to dacitic lavas erupted over the last 350??kyr from the Mount Adams volcanic field has been analyzed for U-Th isotope compositions to evaluate the roles of mantle versus crustal components during magma genesis. All of the lavas have (230Th/238U) > 1 and span a large range in (230Th/232Th) ratios, and most basalts have higher (230Th/232Th) ratios than andesites and dacites. Several of the lavas contain antecrysts (crystals of pre-existing material), yet internal U-Th mineral isochrons from six of seven lavas are indistinguishable from their eruption ages. This indicates a relatively brief period of time between crystal growth and eruption for most of the phenocrysts (olivine, clinopyroxene, plagioclase, magnetite) prior to eruption. One isochron gave a crystallization age that is ~ 20-25??ka older than its corresponding eruptive age, and is interpreted to reflect mixing of older and juvenile crystals or a protracted period of magma storage in the crust. Much of the eruptive volume since 350??ka consists of lavas that have small to moderate 230Th excesses (2-16%), which are likely inherited from melting of a garnet-bearing intraplate ("OIB-like") mantle source. Following melt generation and subsequent migration through the upper mantle, most Mt. Adams magmas interacted with young, mafic lower crust, as indicated by 187Os/188Os ratios that are substantially more radiogenic than the mantle or those expected via mixing of subducted material and the mantle wedge. Moreover, Os-Th isotope variations suggest that unusually large 230Th excesses (25-48%) and high 187Os/188Os ratios in some peripheral lavas reflect assimilation of small degree partial melts of pre-Quaternary basement that had residual garnet or Al-rich clinopyroxene. Despite the isotopic evidence for lower crustal assimilation, these processes are not generally recorded in the erupted phenocrysts, indicating that the crystal record of the deep-level 'cryptic' processes has been

  3. Assessment of natural radionuclides concentration from {sup 238}U and {sup 232}Th series in Virginia and Burley varieties of Nicotiana tabacum L; Avaliacao da concentracao dos radionuclideos naturais das series do {sup 238}U e {sup 232}Th nas variedades Burley e Virginia da Nicotiana tabacum L.

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Carolina Fernanda da

    2015-07-01

    Brazil is the largest exporter and second largest producer of tobacco worldwide, according to the crop production of 2013/2014. The tobacco plant (Nicotiana tabacum L.) is used to manufacture all derivatives and the chemical composition of the resulting tobacco products varies with the type of tobacco leaves, how they are grown, the region where they are cultivated, the characteristics of preparation (compression, filter and paper) and the temperature variations resulting from the incomplete combustion of tobacco. Tobacco products are extensively used throughout the world, and the most consumed are cigarettes, cigars and narghile. The damaging effects that these products cause to human health are discussed globally, and many surveys are performed with the aim of relating the use of these products with various illnesses. There is a lack of information about the radiological characterization of the tobacco plant both in international and Brazilian literature. The objective of this study was to determine the concentration of radionuclides {sup 238}U, {sup 234}U, {sup 230}Th, {sup 22}'6Ra, {sup 210}Pb and {sup 210}Po, members from the {sup 238}U decay series, and the radionuclides {sup 232}Th and {sup 228}Ra members of the {sup 232}Th decay series in the varieties Burley and Virginia, which are the most cultivated in Brazil. Plants from these varieties were cultivated in pots with organic substrate and fertilizer and also acquired from the producers and analyzed by alpha spectrometry for U and Th isotopes and {sup 210}Po determination, and gross alpha and beta counting, {sup 228}Ra, {sup 226}Ra and {sup 210}Pb determination. The whole plant, from both places, was analyzed; root, stem, leaves, as well as the organic substrate, the fertilizers, and the soil. The results for U and Th isotopes presented values below the detection limits of the methods to the leaves and stems of all plants analyzed, with measurable results only in roots, soil, and substrate. The

  4. Nondestructive determination of the 238U content in mental uranium sample by using the activation method%用活化法无损测定金属铀样品中238U的含量

    Institute of Scientific and Technical Information of China (English)

    汪超; 肖军; 王攀; 李映映; 李子越; 罗小兵

    2016-01-01

    238U 作为一种重要的裂变材料,其含量的准确测定在裂变产额数据测量中具有重要意义。在四川大学2.5 MeV质子静电加速器上,利用T(p,n)3He反应产生的483 keV单能中子照射金属铀样品,对照射后生成放射性核素239Np的特征γ射线进行测量,利用已知的238U(n,γ)俘获截面数据实现了对238U含量的准确测量。对影响测量结果准确性的因素做了细致分析,采用蒙特卡罗方法应用软件 MCNPX (Monte Carlo N-Particle eXtended)对中子的多次散射效应和中子注量衰减效应进行了修正,对γ射线在样品中的自吸收也进行了修正,修正后的实验结果是2.8842 g金属铀含5.7128×1021个238U原子,实验结果的不确定度是4.1%。%Background: As a kind of important fission material, the accurate quantification of 238U is of great significance in the measurement of fission yield data. Purpose:The aim is to nondestructively measure the content of 238U by using the activation method. Methods:Neutron of 483-keV produced by the reaction of T(p,n)3He induces 238U occurring radiative capture reaction on the 2.5-MeV electrostatic accelerator of Sichuan University. The atomic number of 238U in uranium samples is measured by using 278-keV gamma ray of 239Np on the detector of high purity germanium (HPGe) and the data of capture cross section. Results: The deflections which were caused by multiple scattering and self-shielding of the target and sample in the experiment were corrected with MCNPX (Monte Carlo N-Particle eXtended). The result of the experiment is that the atomic number of 238U in the 2.884 2-g metal uranium is 5.712 8×1021. Conclusion:The uncertainty of the experimental result is 4.1%. We can reduce the effect of multiple scattering effects and self-shielding by decreasing the thickness of the bottom lining, target tube, water layer and cladding material of the sample.

  5. Correlation of the activity of the {sup 238} U in soil and {sup 222} Rn in domiciles, with the rocks of cities of the Estado de Chihuahua; Correlacion de la actividad del {sup 238} U en suelo y {sup 222} Rn en domicilios, con las rocas de ciudades del Estado de Chihuahua

    Energy Technology Data Exchange (ETDEWEB)

    Colmenero S, L.; Villalba, L.; Montero C, M.E. [Centro de Investigacion en Materiales Avanzados (CIMAV), Av. Miguel de Cervantes 120 C.P. 31109 Chihuahua (Mexico)]. e-mail: luis.colmenero@cimav.edu.mx

    2004-07-01

    The state of Chihuahua has numerous locations of uranium, being Pena Blanca the great and more important location of the country. Diverse rock types with important quantities of uranium are distributed by the whole state. The igneous extrusive acid rocks are those that have bigger quantity of uranium, like they are the rhyolites and dacites and these rocks are located in enough proportion by the whole state. Some of the main cities of the state are near to locations or uraniferous rocks, as Aldama, Nuevo Casas Grandes, Chihuahua, Jimenez and Bocoyna, other important cities are not near important locations. It was determined specific activity by gamma spectroscopy of the series of the {sup 238} U in soils and determination of the radon concentration in domiciles of the main cities of the state. They were found high specific activity values in soil in eight of the thirteen analyzed cities and important radon concentrations in three cities. It was found relationship among the specific activity in soil in near cities to uraniferous locations. (Author)

  6. CREATING THE KULTUK POLYGON FOR EARTHQUAKE PREDICTION: VARIATIONS OF (234U/238U AND 87SR/86SR IN GROUNDWATER FROM ACTIVE FAULTS AT THE WESTERN SHORE OF LAKE BAIKAL

    Directory of Open Access Journals (Sweden)

    S. V. Rasskazov

    2015-12-01

    Full Text Available Introduction. Determinations of (234U/238U in groundwater samples are used for monitoring current deformations in active faults (parentheses denote activity ratio units. The cyclic equilibrium of activity ratio 234U/238U≈≈(234U/238U≈γ≈1 corresponds to the atomic ratio ≈5.47×10–5. This parameter may vary due to higher contents of 234U nuclide in groundwater as a result of rock deformation. This effect discovered by P.I. Chalov and V.V. Cherdyntsev was described in [Cherdyntsev, 1969, 1973; Chalov, 1975; Chalov et al., 1990; Faure, 1989]. In 1970s and 1980s, only quite laborious methods were available for measuring uranium isotopic ratios. Today it is possible to determine concentrations and isotopic ration of uranium by express analytical techniques using inductively coupled plasma mass spectrometry (ICP‐MS [Halicz et al., 2000; Shen et al., 2002; Cizdziel et al., 2005; Chebykin et al., 2007]. Sets of samples canbe efficiently analysed by ICP‐MS, and regularly collected uranium isotope values can be systematized at a new quality level for the purposes of earthquake prediction. In this study of (234U/238U in groundwater at the Kultuk polygon, we selected stations of the highest sensitivity, which can ensure proper monitoring of the tectonic activity of the Obruchev and Main Sayan faults. These two faults that limit the Sharyzhalgai block of the crystalline basement of the Siberian craton in the south are conjugated in the territory of the Kultuk polygon (Fig 1. Forty sets of samples taken from 27 June 2012 to 28 January 2014 were analysed, and data on 170 samples are discussed in this paper.Methods. Isotope compositions of uranium and strontium were determined by methods described in [Chebykin et al., 2007; Pin et al., 1992] with modifications. Analyses of uranium by ISP‐MS technique were performed using an Agilent 7500ce quadrapole mass spectrometer of the Ultramicroanalysis Collective Use Centre; analyses of

  7. Mass measurements of {sup 238}U-projectile fragments for the first time with a multiple-reflection time-of-flight mass spectrometer

    Energy Technology Data Exchange (ETDEWEB)

    Ebert, Jens

    2016-07-01

    Mass measurements of short-lived uranium projectile fragments were performed for the first time with a Multiple-Reflexion-Time-of-Flight Mass Spectrometer (MR-TOF-MS). A major part of this doctoral work was a novel development of a data analysis method for the MR-TOF-MS mass measurements of exotic nuclei at the fragment separator FRS at GSI. The developed method was successfully applied to the data obtained from two pilot experiments with the MR-TOF-MS at the FRS in 2012 and 2014. A substantial upgrade of the experimental setup of the MR-TOF-MS was also performed in the frame work of this doctoral thesis after the first run. In the experiments projectile fragments were created with 1000 MeV/u {sup 238}U ions in a Be/Nb target at the entrance of the in-flight separator FRS. The exotic nuclei were spatially separated, energy bunched and slowed down with the ion-optical system of the FRS combined with monoenergetic and homogeneous degraders. At the final focal plane of the FRS the fragments were completely slowed down and thermalized in a cryogenic stopping cell (CSC) filled with 3-5 mg/cm{sup 2} pure helium gas. The exotic nuclei were fast extracted from the CSC to enable mass measurements of very short-lived fragments with the MR-TOF-MS. The achievement of this goal was successfully demonstrated with the mass measurement of {sup 220}Ra ions with a half-life of 17.9 ms and 11 detected events. The mass measurements of the isobars {sup 211}Fr, {sup 211}Po and {sup 211}Rn have clearly demonstrated the scientific potential of the MR-TOF-MS for the investigation of exotic nuclei and the power of the data analysis system. Difficult measurements with overlapping mass distributions with only a few counts in the measured spectra were the challenge for the new data analysis method based on the maximum likelihood method. The drifts during the measurements were corrected with the developed time-resolved calibration method. After the improvements of the setup as a consequence of

  8. Improved 206Pb/238U microprobe geochronology by the monitoring of a trace-element-related matrix effect; SHRIMP, ID-TIMS, ELA-ICP-MS and oxygen isotope documentation for a series of zircon standards

    Science.gov (United States)

    Black, L.P.; Kamo, S.L.; Allen, C.M.; Davis, D.W.; Aleinikoff, J.N.; Valley, J.W.; Mundil, R.; Campbell, I.H.; Korsch, R.J.; Williams, I.S.; Foudoulis, C.

    2004-01-01

    Precise isotope dilution-thermal ionisation mass spectrometry (ID-TIMS) documentation is given for two new Palaeozoic zircon standards (TEMORA 2 and R33). These data, in combination with results for previously documented standards (AS3, SL13, QGNG and TEMORA 1), provide the basis for a detailed investigation of inconsistencies in 206Pb/238U ages measured by microprobe. Although these ages are normally consistent between any two standards, their relative age offsets are often different from those established by ID-TIMS. This is true for both sensitive high-resolution ion-microprobe (SHRIMP) and excimer laser ablation-inductively coupled plasma-mass spectrometry (ELA-ICP-MS) dating, although the age offsets are in the opposite sense for the two techniques. Various factors have been investigated for possible correlations with age bias, in an attempt to resolve why the accuracy of the method is worse than the indicated precision. Crystallographic orientation, position on the grain-mount and oxygen isotopic composition are unrelated to the bias. There are, however, striking correlations between the 206Pb/238U age offsets and P, Sm and, most particularly, Nd abundances in the zircons. Although these are not believed to be the primary cause of this apparent matrix effect, they indicate that ionisation of 206Pb/238U is influenced, at least in part, by a combination of trace elements. Nd is sufficiently representative of the controlling trace elements that it provides a quantitative means of correcting for the microprobe age bias. This approach has the potential to reduce age biases associated with different techniques, different instrumentation and different standards within and between laboratories. Crown Copyright ?? 2004 Published by Elsevier B.V. All rights reserved.

  9. Neutron capture cross section measurement of 238U at the CERN n_TOF facility in the energy region from 1 eV to 700 keV

    Science.gov (United States)

    Mingrone, F.; Massimi, C.; Vannini, G.; Colonna, N.; Gunsing, F.; Žugec, P.; Altstadt, S.; Andrzejewski, J.; Audouin, L.; Barbagallo, M.; Bécares, V.; Bečvář, F.; Belloni, F.; Berthoumieux, E.; Billowes, J.; Bosnar, D.; Brugger, M.; Calviani, M.; Calviño, F.; Cano-Ott, D.; Carrapiço, C.; Cerutti, F.; Chiaveri, E.; Chin, M.; Cortés, G.; Cortés-Giraldo, M. A.; Diakaki, M.; Domingo-Pardo, C.; Duran, I.; Dressler, R.; Eleftheriadis, C.; Ferrari, A.; Fraval, K.; Ganesan, S.; García, A. R.; Giubrone, G.; Gonçalves, I. F.; González-Romero, E.; Griesmayer, E.; Guerrero, C.; Hernández-Prieto, A.; Jenkins, D. G.; Jericha, E.; Kadi, Y.; Käppeler, F.; Karadimos, D.; Kivel, N.; Koehler, P.; Kokkoris, M.; Krtička, M.; Kroll, J.; Lampoudis, C.; Langer, C.; Leal-Cidoncha, E.; Lederer, C.; Leeb, H.; Leong, L. S.; Lo Meo, S.; Losito, R.; Mallick, A.; Manousos, A.; Marganiec, J.; Martínez, T.; Mastinu, P. F.; Mastromarco, M.; Mendoza, E.; Mengoni, A.; Milazzo, P. M.; Mirea, M.; Mondalaers, W.; Paradela, C.; Pavlik, A.; Perkowski, J.; Plompen, A.; Praena, J.; Quesada, J. M.; Rauscher, T.; Reifarth, R.; Riego, A.; Robles, M. S.; Rubbia, C.; Sabaté-Gilarte, M.; Sarmento, R.; Saxena, A.; Schillebeeckx, P.; Schmidt, S.; Schumann, D.; Tagliente, G.; Tain, J. L.; Tarrío, D.; Tassan-Got, L.; Tsinganis, A.; Valenta, S.; Variale, V.; Vaz, P.; Ventura, A.; Vermeulen, M. J.; Vlachoudis, V.; Vlastou, R.; Wallner, A.; Ware, T.; Weigand, M.; Weiß, C.; Wright, T.; n TOF Collaboration

    2017-03-01

    The aim of this work is to provide a precise and accurate measurement of the 238U(n ,γ ) reaction cross section in the energy region from 1 eV to 700 keV. This reaction is of fundamental importance for the design calculations of nuclear reactors, governing the behavior of the reactor core. In particular, fast reactors, which are experiencing a growing interest for their ability to burn radioactive waste, operate in the high energy region of the neutron spectrum. In this energy region most recent evaluations disagree due to inconsistencies in the existing measurements of up to 15%. In addition, the assessment of nuclear data uncertainty performed for innovative reactor systems shows that the uncertainty in the radiative capture cross section of 238U should be further reduced to 1-3% in the energy region from 20 eV to 25 keV. To this purpose, addressed by the Nuclear Energy Agency as a priority nuclear data need, complementary experiments, one at the GELINA and two at the n_TOF facility, were proposed and carried out within the 7th Framework Project ANDES of the European Commission. The results of one of these 238U(n ,γ ) measurements performed at the n_TOF CERN facility are presented in this work. The γ -ray cascade following the radiative neutron capture has been detected exploiting a setup of two C6D6 liquid scintillators. Resonance parameters obtained from this work are on average in excellent agreement with the ones reported in evaluated libraries. In the unresolved resonance region, this work yields a cross section in agreement with evaluated libraries up to 80 keV, while for higher energies our results are significantly higher.

  10. {sup 90}Sr, {sup 238}U, {sup 234}U, {sup 137}Cs, {sup 40}K and {sup 239/240}Pu in Emmental type cheese produced in different regions of Western Europe

    Energy Technology Data Exchange (ETDEWEB)

    Froidevaux, P. E-mail: pascal.froidevaux@inst.hospvd.ch; Geering, J.-J.; Pillonel, L.; Bosset, J.-O.; Valley, J.-F

    2004-07-01

    A method is presented for the determination of {sup 90}Sr and uranium in Emmental type cheese collected in dairy plants from different European countries. Results display a significant correlation (r=0.708, Student t-test=6.02) between the {sup 90}Sr content of the cheese and the altitude of grazing. The highest {sup 90}Sr activity is 1.13 Bq kg{sup -1} of cheese and the lowest is 0.29 Bq kg{sup -1}. Uranium activity is very low with a highest {sup 238}U value of 27 mBq kg{sup -1}. In addition, {sup 234}U/{sup 238}U ratio shows a large enrichment in {sup 234}U for every location. Without any significant indication of the geographic origin of the cheese, this enrichment is believed to be due to the geological features of the pasture, soil and underground water. These results tend to prove that the contamination of milk by uranium originates principally from the water that the cows drink instead of the forage. This finding may have a great importance in models dealing with dairy food contamination by radionuclides following a nuclear accident. Also, the {sup 90}Sr content and to a lesser extent the {sup 234}U/{sup 238}U ratio could be used to trace the authenticity of the origin of the cheese. {sup 137}Cs activity is lower than the detection limit of 0.1 Bq kg{sup -1} in all the samples collected (n=20). Based on natural {sup 40}K activity in cheese (15-21 Bq kg{sup -1}), the decontamination factor for the alkaline cations from milk to cheese is about 20. Plutonium activity stays below the detection limit of 0.3 mBq kg{sup -1}.

  11. Measurement of neutron-induced fission cross-sections of Th232, U238, U233 and Np237 relative to U235 from 1 MeV to 200 MeV

    Energy Technology Data Exchange (ETDEWEB)

    Shcherbakov, O.A.; Laptev, A.B.; Petrov, G.A. [Petersburg Nuclear Physics Inst., Gatchina, Leningrad district (Russian Federation); Fomichev, A.V.; Donets, A.Y.; Osetrov, O.I.

    1998-11-01

    The measurements of neutron-induced cross-section ratios for Th232, U238, U233 and Np237 relative to U235 have been carried out in the energy range from 1 MeV up to 200 MeV using the neutron time-of-flight spectrometer GNEIS based on 1 GeV proton synchrocyclotron. Below 20 MeV, the results of present measurements are roughly in agreement with evaluated data though there are some discrepances to be resolved. (author)

  12. Measurement of the 238U neutron-capture cross section and gamma-emission spectra from 10 eV to 100 keV using the DANCE detector at LANSCE

    Energy Technology Data Exchange (ETDEWEB)

    Ullmann, John L [Los Alamos National Laboratory; Couture, A J [Los Alamos National Laboratory; Keksis, A L [Los Alamos National Laboratory; Vieira, D J [Los Alamos National Laboratory; O' Donnell, J M [Los Alamos National Laboratory; Jandel, M [Los Alamos National Laboratory; Haight, R C [Los Alamos National Laboratory; Rundberg, R S [Los Alamos National Laboratory; Kawano, T [Los Alamos National Laboratory; Chyzh, A [NORTH CAROLINA STATE UNIV; Baramsai, B [NORTH CAROLINA STATE UNIV; Wu, C Y [LLNL; Mitchell, G E [NORTH CAROLINA STATE UNIV; Becker, J A [LLNL; Krticka, M [CHARLES UNIV

    2010-01-01

    A careful new measurement of the {sup 238}U(n,{gamma}) cross section from 10 eV to 100 keV has been made using the DANCE detector at LANSCE. DANCE is a 4{pi} calorimetric scintillator array consisting of 160 BaF{sub 2} crystals. Measurements were made on a 48 mg/cm{sup 2} depleted uranium target. The cross sections are in general good agreement with previous measurements. The gamma-ray emission spectra, as a function of gamma multiplicity, were also measured and compared to model calculations.

  13. Uncertainty analyses in the resolved resonance region of {sup 235}U, {sup 238}U, and {sup 239}Pu with the Reich-Moore R-matrix theory for JENDL-3.2

    Energy Technology Data Exchange (ETDEWEB)

    Kawano, Toshihiko [Kyushu University, Interdisciplinary Graduate School of Engineering Sciences, Kasuga, Fukuoka (Japan); Shibata, Keiichi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2002-08-01

    A simple method to estimate covariances for resolved resonance parameters was developed. Although a large number of resolved resonances are observed for major actinides, uncertainties in averaged cross sections are more important than those in resonance parameters in reactor calculations. The method developed here derives a covariance matrix for the resolved resonance parameters which gives an appropriate uncertainty of the averaged cross sections. The method was adopted to evaluate the covariance data for {sup 235}U, {sup 238}U, and {sup 239}Pu resonance parameters in JENDL-3.2, with the Reich-Moore R-matrix formula. (author)

  14. Determination of uranium isotopes ({sup 235}U, {sup 238}U) and trace elements (Cd, Pb, Cu and As) in bottled drinking water by Icp-SFMS; Determinacion de isotopos de uranio ({sup 235}U, {sup 238}U) y elementos traza (Cd, Pb, Cu y As) en agua embotellada para beber por ICP-SFMS

    Energy Technology Data Exchange (ETDEWEB)

    Lara A, N.; Hernandez M, H.; Romero G, E. T.; Kuri de la C, A.; Perez B, M. A., E-mail: nancy.lara@inin.gob.mx [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2016-09-15

    In the present work we propose an optimized method for the quantification of uranium isotopes ({sup 235}U, 2{sup 38}U) and the elements Cd, Pb, Cu and As in bottled water for drinking at trace levels of concentration. Based on the multi-element detection capability, the high sensitivity and resolution that the Mass Spectrometry with Magnetic Sector with Inductively Coupled Plasma Source (Icp-SFMS) technique offers; the high, medium and low resolution analysis conditions for the elements under study were established and optimized using and Element 2/Xr equipment and the 23 multi-elemental Certified Reference Material (CRM). The analysis method was validated using the standard reference material Nist 1643d and CRM mono-elemental s as external standards for the quantification of the analytes. Samples, targets and CRM were acidified with 2% of HNO{sub 3} and analyzed without pretreatment under the established analysis conditions. The results obtained show concentrations of {sup 235}U, {sup 238}U, {sup 111}Cd, {sup 208}Pb, {sup 63}Cu and {sup 75}As in the range of μg L{sup -1}, the linearity obtained from the calibration curves for each element has correlation coefficients < 0.99 in all cases, the accuracy of the method in terms of percent relative standard deviation (RSD %) was less than 5%, the mean recovery rate of Nist 1643d ranged from 96.46% to 101.12%. The optimization of the method guarantees the stability and calibration of the equipment throughout the analysis, as well as the ability to resolve interferences. In conclusion, the method proposed using Icp-SFMS offers the advantages of being fast and simple for the multi-elemental analysis in water at trace levels, with low limits of quantification and detection, with good linearity, accuracy, precision and reproducibility to a degree of reliability of 95%. (Author)

  15. 235U, 238U, 232Th, 40K and 137Cs activity concentrations in marine sediments along the northern coast of Oman Sea using high-resolution gamma-ray spectrometry.

    Science.gov (United States)

    Zare, Mohammad Reza; Mostajaboddavati, Mojtaba; Kamali, Mahdi; Abdi, Mohammad Reza; Mortazavi, Mohammad Seddigh

    2012-09-01

    The natural radioactivity levels in sediment samples of the northern coast of Oman Sea, covering the coastal strip from Hormoz canyon to Goatr seaport, as the first time has been determined. The results of measurements will serve as background reference level for Oman Sea coastlines. Sediments from 36 coastal and near shore locations were collected for analysis. Analysis on the collected samples were carried out to determine (235)U, (238)U, (232)Th, (40)K and (137)Cs using two high purity germanium detectors with 38.5% and 55% relative efficiencies. The concentration of (235)U, (238)U, (232)Th, (40)K and (137)Cs in sediment samples ranged between 1.01 and 2.87 Bq/kg, 11.83 and 22.68 Bq/kg, 10.7 and 25.02 Bq/kg, 222.89 and 535.07 Bq/kg and 0.14 and 2.8 Bq/kg, respectively. The radium equivalent activity was well below the defined limit of 370 Bq/kg. The external hazard indices were found to be less than 1, indicating a low dose.

  16. Neutron capture cross section measurement of 238U at the n TOF CERN facility with C6D6 scintillation detectors in the energy region from 1 eV to 700 keV

    CERN Document Server

    Mingrone, F.

    2017-01-01

    The aim of this work is to provide a precise and accurate measurement of the 238U(n,g) reaction cross section in the energy region from 1 eV to 700 keV. This reaction is of fundamental importance for the design calculations of nuclear reactors, governing the behaviour of the reactor core. In particular, fast reactors, which are experiencing a growing interest for their ability to burn radioactive waste, operate in the high energy region of the neutron spectrum. In this energy region most recent evaluations disagree due to inconsistencies in the existing measurements of up to 15%. In addition, the assessment of nuclear data uncertainty performed for innovative reactor systems shows that the uncertainty in the radiative capture cross-section of 238U should be further reduced to 1-3% in the energy region from 20 eV to 25 keV. To this purpose, addressed by the Nuclear Energy Agency as a priority nuclear data need, complementary experiments, one at the GELINA and two at the n_TOF facility, were proposed and carrie...

  17. Neutron capture cross section measurement of $^{238}$U at the n_TOF CERN facility in the energy region from 1 eV to 700 keV

    CERN Document Server

    Mingrone, F; Vannini, G; Colonna, N; Gunsing, F; Zugec, P; Altstadt, S; Andrzejewski, J; Audouin, L; Barbagallo, M; Becares, V; Becvavr, F; Belloni, F; Berthoumieux, E; Billowes, J; Bosnar, D; Brugger, M; Calviani, M; Calvino, F; Cano-Ott, D; Carrapico, C; Cerutti, F; Chiaveri, E; Chin, M; Cortes, G; Cortes-Giraldo, M A; Diakaki, M; Domingo-Pardo, C; Duran, I; Dressler, R; Eleftheriadis, C; Ferrari, A; Fraval, K; Ganesan, S; Garcia, A R; Giubrone, G; Goncalves, I F; Gonzalez-Romero, E; Griesmayer, E; Guerrero, C; Hernandez-Prieto, A; Jenkins, D G; Jericha, E; Kadi, Y; Kappeler, F; Karadimos, D; Kivel, N; Koehler, P; Kokkoris, M; Krticka, M; Kroll, J; Lampoudis, C; Langer, C; Leal-Cidoncha, E; Lederer, C; Leeb, H; Leong, L S; Lo Meo, S; Losito, R; Mallick, A; Manousos, A; Marganiec, J; Martinez, T; Mastinu, P F; Mastromarco, M; Mendoza, E; Mengoni, A; Milazzo, P M; Mirea Horia, M; Mondalaers, W; Paradela, C; Pavlik, A; Perkowski, J; Plompen, A; Praena, J; Quesada, J M; Rauscher, T; Reifarth, R; Riego, A; Robles, M S; Rubbia, C; Sabate-Gilarte, M; Sarmento, R; Saxena, A; Schillebeeckx, P; Schmidt, S; Schumann, D; Tagliente, G; LTain, J; Tarrio, D; Tassan-Got, L; Tsinganis, A; Valenta, S; Variale, V; Vaz, P; Ventura, A; Vermeulen, M J; Vlachoudis, V; Vlastou, R; Wallner, A; Ware, T; Weigand, M; Weiss, C; Wright, T

    2016-01-01

    The aim of this work is to provide a precise and accurate measurement of the $^{238}$U(n,$\\gamma$) reaction cross section in the energy region from 1 eV to 700 keV. This reaction is of fundamental importance for the design calculations of nuclear reactors, governing the behaviour of the reactor core. In particular, fast reactors, which are experiencing a growing interest for their ability to burn radioactive waste, operate in the high energy region of the neutron spectrum. In this energy region most recent evaluations disagree due to inconsistencies in the existing measurements of up to 15%. In addition, the assessment of nuclear data uncertainty performed for innovative reactor systems shows that the uncertainty in the radiative capture cross-section of $^{238}$U should be further reduced to 1-3% in the energy region from 20 eV to 25 keV. To this purpose, addressed by the Nuclear Energy Agency as a priority nuclear data need, complementary experiments, one at the GELINA and two at the n_TOF facility, were pr...

  18. Determination of {sup 234}U and {sup 238}U in seawater samples by alpha spectrometry after concentration of U(VI) onto hydrotalcite and co-precipitation with LaF{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Suc, N.V. [University of Technical Education Ho Chi Minh City (Viet Nam); Bich, T.T. [Center for Nuclear Techniques, Ho Chi Minh City (Viet Nam)

    2013-07-01

    This paper presents a simple and accurate method for determination of uranium isotopes ({sup 234}U and {sup 238}U) in seawater samples using alpha spectrometry. Uranium is pre-concentrated from seawater samples via adsorption on hydrotalcite at pH 6.5. The absorbent is dissolved into 50 ml of 8M HNO{sub 3}; then filtered through a Dowex-1 column. U(VI) in the elution solution is reduced to U(IV) using zinc metal in 4M solution of HCl and then co-precipitated with LaF{sub 3}. The chemical separation efficiency is found to be 97.12 {+-} 2.68%, eliminating the need of using {sup 232}U tracer in other published methods. This method is validated via comparison with results obtained using inductively coupled plasma mass spectrometry (ICP-MS) and neutron activation analysis (NAA) for three seawater samples. (orig.)

  19. Spin-alignment and g-factor measurement of the I{sup {pi}}=12{sup +} isomer in {sup 192}Pb produced in the relativistic-energy fragmentation of a {sup 238}U beam

    Energy Technology Data Exchange (ETDEWEB)

    Kmiecik, M.; Maj, A.; Ciemala, M.; Grebosz, J.; Lach, M.; Maier, K.H.; Mazurek, K.; Meczynski, W.; Myalski, S.; Styczen, J.; Zieblinski, M. [H. Niewodniczanski Inst. of Nuclear Physics PAN, Krakow (Poland); Gerl, J.; Becker, F.; Caceres, L.; Doornenbal, P.; Gorska, M.; Grawe, H.; Kojuharov, I.; Prokopowicz, W.; Saito, N.; Saito, T.R.; Wollersheim, H.J. [GSI, Darmstadt (Germany); Neyens, G.; Mallion, S.; Vermeulen, N. [Inst. voor Kern- en Stralingsfysica, K.U. Leuven (Belgium); Atanasova, L.; Detistov, P. [Univ. of Sofia ' St. Kl. Ohridski' (Bulgaria). Faculty of Physics; Balabanski, D.L. [Univ. degli Studi di Camerino (Italy); INFN sez. Perugia, Dipt. di Fisica, Camerino (Italy); Bulgarian Academy of Sciences, Inst. for Nuclear Research and Nuclear Energy, Sofia (Bulgaria); Bednarczyk, P. [H. Niewodniczanski Inst. of Nuclear Physics PAN, Krakow (Poland); GSI, Darmstadt (Germany); Benzoni, G.; Blasi, N.; Brambilla, S.; Million, B.; Wieland, O. [INFN Sez. di Milano (Italy); Bracco, A.; Camera, F.; Crespi, F.C.L.; Leoni, S.; Montanari, D. [INFN Sez. di Milano (Italy); Univ. degli Studi di Milano (Italy); Chamoli, S.K.; Hass, M.; Lakshmi, S. [Weizman Inst. of Science, Rehovot (Israel); Chmel, S. [Fraunhofer INT, Euskirchen (Germany); Daugas, J.M. [CEA, DAM, DIF, Arpajon Cedex (France); Georgiev, G. [Univ. Paris-Sud 11, CNRS/IN2P3, CSNSM, Orsay-Campus (France); Gladnishki, K. [Univ. of Sofia ' St. Kl. Ohridski' (Bulgaria). Faculty of Physics; Univ. degli Studi di Camerino (Italy); INFN sez. Perugia, Dipt. di Fisica, Camerino (Italy); Hoischen, R.; Rudolph, D. [Lund Univ., Dept. of Physics, Lund (Sweden); Ilie, G. [Univ. zu Koeln, Inst. fuer Kernphysik, Koeln (Germany); National Inst. for Physics and Nuclear Engineering, Bucharest (Romania); Ionescu-Bujor, M. [National Inst. for Physics and Nuclear Engineering, Bucharest (Romania); Jolie, J. [Univ. zu Koeln, Institut fuer Kernphysik, Koeln (Germany)] [and others

    2010-08-15

    The feasibility of measuring g -factors using the TDPAD method applied to high-energy, heavy fragmentation products is explored. The 2623keV I{sup {pi}}=12{sup +} isomer in {sup 192}Pb with {tau}=1.57{mu}s has been produced using the fragmentation of a 1A GeV {sup 238}U beam. The results presented demonstrate for the first time that such heavy nuclei produced in a fragmentation reaction with a relativistic beam are sufficiently well spin-aligned. Moreover, the rather large value of the alignment, 28(10)% of the maximum possible, is preserved during the separation process allowing the determination of magnetic moments. The measured values of the lifetime, {tau}=1.54(9) {mu}s, and the g-factor, g=-0.175(20), agree with the results of previous investigations using fusion-evaporation reactions. (orig.)

  20. Sorption behavior of U(VI), 234U(VI) and 238U(VI) onto fracture-filling clays in Beishan granite, Gansu: Application to selecting the site of high-level radwaste repository in China

    Institute of Scientific and Technical Information of China (English)

    MIN; Maozhong; LUO; Xingzhang; WANG; Ju; JIN; Yuanxin; WAN

    2005-01-01

    The first results of sorption experiments of U(VI), 234U(VI) and 238U(VI) onto original (unpurified) fracture-filling clays from No.1 monzonitic granite intrusion, Beishan area, Gansu Province, China are reported. The monzonitic granite intrusion is a potential location for a high-level radwaste (HLW) repository in China. The present experimental results show that the maximum U(VI) sorption reached 92% at near-neutral Ph and the distribution coefficient (Kd) was 1226 Ml/g. A high sorption capacity of the fracture-filling clays in host rock on radioactive elements is necessary for HLW deep geological disposal repository. No preferential sorption of 234U onto the clays was found. Finally, the sorption of U(VI) onto the clays was also modeled using a surface complexation model.

  1. Potential human health risk by metal(loid)s, 234,238U and 210Po due to consumption of fish from the "Luis L. Leon" Reservoir (Northern México).

    Science.gov (United States)

    Luna-Porres, Mayra Y; Rodríguez-Villa, Marco A; Herrera-Peraza, Eduardo F; Renteria-Villalobos, Marusia; Montero-Cabrera, María E

    2014-06-25

    Concentrations of As, Cu, Fe, Hg, Pb and Zn and activity concentrations from 234,238U and 210Po in water, fillet, liver and gills were determined in three stocked fish species from the Luis L. Leon reservoir, located in Northern Mexico. The considered species were Lepomis cyanellus, Cyprinus carpio and Ictalurus furcatus. 238U and 234U activity concentration (AC) in fillet samples showed values of 0.007-0.014 and 0.01-0.02 Bq∙kg-1 wet weight (ww), respectively. Liver samples for L. cyanellus, C. carpio and I. furcatus present 210Po AC of 1.16-3.26, 0.70-1.13 and 0.93-1.37 Bq∙kg-1 ww. Arsenic, mercury and lead concentration intervals in fillet samples were 0.13-0.39, 0.005-0.126 and 0.009-0.08 mg∙kg-1 ww, respectively, while in gill samples they were 0.11-0.43, 0.002-0.039 and 0.02-0.26 mg∙kg-1 ww. The elemental Bioaccumulation Factor (BAF) for fish tissues with respect to their concentrations in water was determined. L. cyanellus showed the highest BAF values for As and total U, being BAFAs = 37 and 40 L∙kg-1 in fillet and gills, respectively, and BAFU total = 1.5 L∙kg-1 in fillet. I. furcatus showed the highest BAF values for Hg and Pb, being BAFHg = 40 and 13 L∙kg-1 in fillet and gills, and BAFPb = 6.5 and 22 L∙kg-1 in fillet and gills, respectively. Some metal(loid) concentrations are slightly higher than European regulations for fish fillets. The difference in concentrations of metal(loid)s in fillet among the studied species is probably due to their differences in diet and habitat.

  2. Carbon export fluxes and export efficiency in the central Arctic during the record sea-ice minimum in 2012: a joint 234Th/238U and 210Po/210Pb study

    Science.gov (United States)

    Roca-Martí, Montserrat; Puigcorbé, Viena; Rutgers van der Loeff, Michiel M.; Katlein, Christian; Fernández-Méndez, Mar; Peeken, Ilka; Masqué, Pere

    2016-07-01

    The Arctic sea-ice extent reached a record minimum in September 2012. Sea-ice decline increases the absorption of solar energy in the Arctic Ocean, affecting primary production and the plankton community. How this will modulate the sinking of particulate organic carbon (POC) from the ocean surface remains a key question. We use the 234Th/238U and 210Po/210Pb radionuclide pairs to estimate the magnitude of the POC export fluxes in the upper ocean of the central Arctic in summer 2012, covering time scales from weeks to months. The 234Th/238U proxy reveals that POC fluxes at the base of the euphotic zone were very low (2 ± 2 mmol C m-2 d-1) in late summer. Relationships obtained between the 234Th export fluxes and the phytoplankton community suggest that prasinophytes contributed significantly to the downward fluxes, likely via incorporation into sea-ice algal aggregates and zooplankton-derived material. The magnitude of the depletion of 210Po in the upper water column over the entire study area indicates that particle export fluxes were higher before July/August than later in the season. 210Po fluxes and 210Po-derived POC fluxes correlated positively with sea-ice concentration, showing that particle sinking was greater under heavy sea-ice conditions than under partially ice-covered regions. Although the POC fluxes were low, a large fraction of primary production (>30%) was exported at the base of the euphotic zone in most of the study area during summer 2012, indicating a high export efficiency of the biological pump in the central Arctic.

  3. Tracing of natural radionuclides mobility in deep sedimentary environment using radioactive ({sup 234}U/{sup 238}U) disequilibria: application to the Mesozoic formations of the Eastern part of the Paris Basin; Tracage de la mobilite des radionucleides naturels en milieu sedimentaire profond a l'aide des desequilibres radioactifs ({sup 234}U/{sup 238}U): application aux formations mesozoiques de l'est du Bassin de Paris

    Energy Technology Data Exchange (ETDEWEB)

    Deschamps, P

    2003-11-01

    This thesis forms part of the geological investigations undertaken by the French agency for nuclear waste management, ANDRA, around the Meuse/Haute-Marne Underground Research Laboratory (URL) located in the Eastern part of the Paris Basin in order to evaluate the feasibility of high-level radioactive waste repository in deep argilite formations. The aim of the study is to examine the radionuclide migration in the deep Callovo-Oxfordian target argilite layer and its surrounding low- permeability Bathonian and Oxfordian limestone formations in order to assess the long term confining capacities of the sedimentary series. This study is based on measurement of radioactive disequilibria within U-series by Multiple- Collector Inductively Coupled Plasma Mass Spectrometry (MC-ICP-MS). The high precision and accuracy achieved allowed to demonstrate the {sup 234}U/{sup 238}U radioactive equilibrium in the Callovo-Oxfordian argilites. This result shows the uranium immobility in the target formation and provides a strong evidence for the current chemical stability and closure of the system for uranium and most probably for the other actinides. This is a fundamental result with respect to the problematic of disposal of high level radioactive waste in deep geological formation since it provides a in situ indication of the confining capacities of the clayey target formation in the current settings. Conversely, ({sup 234}U/{sup 238}U) disequilibria are systematically observed within zones, located in the surrounding carbonate formations, that are characterized by pressure dissolution structures (stylolites or dissolution seams). These disequilibria provide evidence for a discrete uranium relocation during the last two million years in the vicinity of stylolitic structures. This is a surprising result since it is generally supposed that these deep, low permeability, compact formations behave as closed system at the time scale of the U-series. (author)

  4. 1.4MeV-5MeV中子诱发238U裂变产额测量%Fission Product Yield Measurement of 238 U Induced by 1.4-5 MeV Neutrons

    Institute of Scientific and Technical Information of China (English)

    李映映; 肖军; 王攀; 李子越; 汪超; 罗小兵

    2016-01-01

    238 U fission yield measurement has a significant meaning in nuclear data measurement .This thesis a-dopts1.4 MeV-5 MeV mono -energetic neutrons generated by 2.5 MeV proton electrostatic accelerator to stimulate 238U fission, and then measures the yield of fission product nuclide 135I、133I、105Ru and 91Sr through measuring fission product radioactivity .Neutron flux during irradiation process is determined by activation meth-od .Subsequently , this thesis analyzes multiple components influencing experiment measurement , including cor-rection on neutron′s multiple scattering and self -shielding effect in target head and sample on the basis of MC-NPX program as well as correction on sample′s self-absorption of γ-ray.Typical deviation of yield data is concluded as 3.5%.Finally, this thesis compares measurement consequences with existing fission yield data .%238 U裂变产额测量工作在核数据测量中有着重要意义,本工作利用2.5MeV质子静电加速器产生的1.4MeV-5MeV单能中子诱发238 U裂变,通过对裂变产物放射性的测量对裂变产物核素135 I、133 I、105 Ru和91 Sr的产额进行了测定。照射过程中中子通量用活化法确定。分析了影响实验测量的多个因素,包括用MCNPX程序对中子在靶头及样品中的多次散射和自屏蔽效应进行了修正,对γ射线在样品中的自吸收进行修正等。得到产额数据典型误差为3.5%,最后把测量结果与已有的裂变产额数据进行比对。

  5. Potential Human Health Risk by Metal(loid)s, 234,238U and 210Po due to Consumption of Fish from the “Luis L. Leon” Reservoir (Northern México)

    Science.gov (United States)

    Luna-Porres, Mayra Y.; Rodríguez-Villa, Marco A.; Herrera-Peraza, Eduardo F.; Renteria-Villalobos, Marusia; Montero-Cabrera, María E.

    2014-01-01

    Concentrations of As, Cu, Fe, Hg, Pb and Zn and activity concentrations from 234,238U and 210Po in water, fillet, liver and gills were determined in three stocked fish species from the Luis L. Leon reservoir, located in Northern Mexico. The considered species were Lepomis cyanellus, Cyprinus carpio and Ictalurus furcatus. 238U and 234U activity concentration (AC) in fillet samples showed values of 0.007–0.014 and 0.01–0.02 Bq∙kg−1 wet weight (ww), respectively. Liver samples for L. cyanellus, C. carpio and I. furcatus present 210Po AC of 1.16–3.26, 0.70–1.13 and 0.93–1.37 Bq∙kg−1 ww. Arsenic, mercury and lead concentration intervals in fillet samples were 0.13–0.39, 0.005–0.126 and 0.009–0.08 mg∙kg−1 ww, respectively, while in gill samples they were 0.11–0.43, 0.002–0.039 and 0.02–0.26 mg∙kg−1 ww. The elemental Bioaccumulation Factor (BAF) for fish tissues with respect to their concentrations in water was determined. L. cyanellus showed the highest BAF values for As and total U, being BAFAs = 37 and 40 L∙kg−1 in fillet and gills, respectively, and BAFU total = 1.5 L∙kg−1 in fillet. I. furcatus showed the highest BAF values for Hg and Pb, being BAFHg = 40 and 13 L∙kg−1 in fillet and gills, and BAFPb = 6.5 and 22 L∙kg−1 in fillet and gills, respectively. Some metal(loid) concentrations are slightly higher than European regulations for fish fillets. The difference in concentrations of metal(loid)s in fillet among the studied species is probably due to their differences in diet and habitat. PMID:24968208

  6. Potential Human Health Risk by Metal(loids, 234,238U and 210Po due to Consumption of Fish from the “Luis L. Leon” Reservoir (Northern México

    Directory of Open Access Journals (Sweden)

    Mayra Y. Luna-Porres

    2014-06-01

    Full Text Available Concentrations of As, Cu, Fe, Hg, Pb and Zn and activity concentrations from 234,238U and 210Po in water, fillet, liver and gills were determined in three stocked fish species from the Luis L. Leon reservoir, located in Northern Mexico. The considered species were Lepomis cyanellus, Cyprinus carpio and Ictalurus furcatus. 238U and 234U activity concentration (AC in fillet samples showed values of 0.007–0.014 and 0.01–0.02 Bq∙kg−1 wet weight (ww, respectively. Liver samples for L. cyanellus, C. carpio and I. furcatus present 210Po AC of 1.16–3.26, 0.70–1.13 and 0.93–1.37 Bq∙kg−1 ww. Arsenic, mercury and lead concentration intervals in fillet samples were 0.13–0.39, 0.005–0.126 and 0.009–0.08 mg∙kg−1 ww, respectively, while in gill samples they were 0.11–0.43, 0.002–0.039 and 0.02–0.26 mg∙kg−1 ww. The elemental Bioaccumulation Factor (BAF for fish tissues with respect to their concentrations in water was determined. L. cyanellus showed the highest BAF values for As and total U, being BAFAs = 37 and 40 L∙kg−1 in fillet and gills, respectively, and BAFU total = 1.5 L∙kg−1 in fillet. I. furcatus showed the highest BAF values for Hg and Pb, being BAFHg = 40 and 13 L∙kg−1 in fillet and gills, and BAFPb = 6.5 and 22 L∙kg−1 in fillet and gills, respectively. Some metal(loid concentrations are slightly higher than European regulations for fish fillets. The difference in concentrations of metal(loids in fillet among the studied species is probably due to their differences in diet and habitat.

  7. Influences of parameter uncertainties within the ICRP-66 respiratory tract model: regional tissue doses for 239PuO2 and 238UO2/238U3O8.

    Science.gov (United States)

    Farfán, Eduardo B; Huston, Thomas E; Bolch, W Emmett; Vernetson, William G; Bolch, Wesley E

    2003-04-01

    This paper extends an examination of the influence of parameter uncertainties on regional doses to respiratory tract tissues for short-ranged alpha particles using the ICRP-66 respiratory tract model. Previous papers examined uncertainties in the deposition and clearance aspects of the model. The critical parameters examined in this study included target tissue depths, thicknesses, and masses, particularly within the thoracic or lung regions of the respiratory tract. Probability density functions were assigned for the parameters based on published data. The probabilistic computer code LUDUC (Lung Dose Uncertainty Code) was used to assess regional and total lung doses from inhaled aerosols of 239PuO2 and 238UO2/238U3O8. Dose uncertainty was noted to depend on the particle aerodynamic diameter. Additionally, dose distributions were found to follow a lognormal distribution pattern. For 239PuO2 and 238UO2/238U3O8, this study showed that the uncertainty in lung dose increases by factors of approximately 50 and approximately 70 for plutonium and uranium oxides, respectively, over the particle size range from 0.1 to 20 microm. For typical exposure scenarios involving both radionuclides, the ratio of the 95% dose fractile to the 5% dose fractile ranged from approximately 8-10 (corresponding to a geometric standard deviation, or GSD, of about 1.7-2) for particle diameters of 0.1 to 1 microm. This ratio increased to about 370 for plutonium oxide (GSD approximately 4.5) and to about 600 for uranium oxide (GSD approximately 5) as the particle diameter approached 20 microm. However, thoracic tissue doses were quite low at larger particle sizes because most of the deposition occurred in the extrathoracic airways. For 239PuO2, median doses from LUDUC were found be in general agreement with those for Reference Man (via deterministic LUDEP 2.0 calculations) in the particle range of 0.1 to 5 microm. However, median doses to the basal cell nuclei of the bronchial airways (BB

  8. The cumulative effect of three decades of phosphogypsum amendments in reclaimed marsh soils from SW Spain: {sup 226}Ra, {sup 238}U and Cd contents in soils and tomato fruit

    Energy Technology Data Exchange (ETDEWEB)

    Abril, Jose-Maria [Dpto. Fisica Aplicada I, Universidad de Sevilla, EUITA, Ctra Utrera Km 1, 41013 Seville (Spain); Garcia-Tenorio, Rafael [Dpto. Fisica Aplicada II, Universidad de Sevilla, ETSA, Avda. Reina Mercedes s/n, 41012 Seville (Spain); Enamorado, Santiago M. [Dpto. Fisica Aplicada I, Universidad de Sevilla, EUITA, Ctra Utrera Km 1, 41013 Seville (Spain); Hurtado, M. Dolores; Andreu, Luis; Delgado, Antonio [Dpto. Ciencias Agroforestales, Universidad de Sevilla, EUITA, Ctra Utrera Km 1, 41013, Seville (Spain)

    2008-09-15

    Phosphogypsum (PG), a by-product of the phosphate fertiliser industries, has been applied as soil amendment to reduce Na saturation in soils, as in the reclaimed marsh area from SW Spain, where available PG has a typical fingerprint of 710 {+-} 40 Bq kg{sup -1} of {sup 226}Ra, 165 {+-} 15 Bq kg{sup -1} of {sup 238}U and 2.8 {+-} 0.4 mg kg{sup -1} of Cd. This work was focussed on the cumulative effects of PG amendments on the enrichment of these pollutants in cultivated soils and plants (Lycopersicum esculentum Mill L.) from the area studied, where PG has been applied since 1978 at recommended rates of 20-25 Mg ha{sup -1} every 2-3 years. A field experiment was conducted over three years to compare activity concentrations of {sup 226}Ra ({sup 214}Pb) and {sup 238}U ({sup 234}Th) in non-reclaimed soils, reclaimed soils with no additional PG application, and reclaimed soils with two additional PG applications. A non-significant effect of two PG amendments (in three years) was observed when compared with non-amended reclaimed plots. Nevertheless, a significant (p < 0.05) enrichment of {sup 226}Ra was observed in the surface horizon (0-30 cm) of reclaimed plots relative to deeper horizons and also when compared with the surface horizon of non-reclaimed soil (p < 0.05), thereby revealing the cumulative effect of three decades of PG applications. Furthermore, the effect of a continuous application of PG was studied by analysing soils and tomato fruits from six commercial farms with different cumulative rates of PG applied. Cadmium concentrations in tomatoes, which were one order of magnitude higher than those found in tomatoes from other areas in South Spain, were positively correlated (r = 0.917*) with {sup 226}Ra-concentration in soils, which can be considered an accurate index of the cumulative PG rate of each farm.

  9. Estimation of covariances of {sup 16}O, {sup 23}Na, Fe, {sup 235}U, {sup 238}U and {sup 239}Pu neutron nuclear data in JENDL-3.2

    Energy Technology Data Exchange (ETDEWEB)

    Shibata, Keiichi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Nakajima, Yutaka; Kawano, Toshihiko; Oh, Soo-Youl; Matsunobu, Hiroyuki; Murata, Toru

    1997-10-01

    Covariances of nuclear data have been estimated for 6 nuclides contained in JENDL-3.2. The nuclides considered are {sup 16}O, {sup 23}Na, Fe, {sup 235}U, {sup 238}U, and {sup 239}Pu, which are regarded as important for the nuclear design study of fast reactors. The physical quantities for which covariances are deduced are cross sections, resolved and unresolved resonance parameters, and the first order Legendre-polynomial coefficient for the angular distribution of elastically scattered neutrons. As for {sup 235}U, covariances were obtained also for the average number of neutrons emitted in fission. The covariances were estimated by using the same methodology that had been used in the JENDL-3.2 evaluation in order to keep a consistency between mean values and their covariances. The least-squares fitting code GMA was used in estimating covariances for reactions of which JENDL-3.2 cross sections had been evaluated by taking account of measurements. In nuclear model calculations, the covariances were calculated by the KALMAN system. The covariance data obtained were compiled in the ENDF-6 format, and will be put into the JENDL-3.2 Covariance File which is one of JENDL special purpose files. (author). 193 refs.

  10. Beta and gamma decay heat measurements between 0.1s-50,000s for neutron fission of {sup 235}U, {sup 238}U and {sup 239}Pu. Progress report, March 1, 1993--January 31, 1994

    Energy Technology Data Exchange (ETDEWEB)

    Schier, W.A.; Couchell, G.P.

    1994-06-01

    Decay heat measurements following the fast fission of {sup 238}U are well underway. The He-jet system and spectrometers were moved to the 1 MW research reactor to gain sufficient fast neutron flux for these measurements. On the Van de Graaff accelerator, the He-jet capillary has been shortened so that beta and gamma measurements following the thermal neutron fission of {sup 235}U could be made down to delay times near 0.1 s. Gamma-ray response functions are now well characterized for gamma energies up to 1.5 MeV for our large Nal spectrometer. Such response functions out to high energies are needed to extract energy distributions of our measured gamma spectra. The response function unfolding program, FERD-PC, has been operated successfully with trial spectra. Comparisons of individual fission products for {sup 235}U(n{sub th}f) with ENDF/B-VI at short delay times suggest several improvements to the data base particularly in production probabilities. The new data acquisition and data analysis systems have arrived and will soon be brought on line extending considerably the capabilities of our research group.

  11. Neutron Resonance Parameters of 238U and the Calculated Cross Sections from the Reich-Moore Analysis of Experimental Data in the Neutron Energy Range from 0 keV to 20 keV

    Energy Technology Data Exchange (ETDEWEB)

    Derrien, H

    2005-12-05

    The neutron resonance parameters of {sup 238}U were obtained from a SAMMY analysis of high-resolution neutron transmission measurements and high-resolution capture cross section measurements performed at the Oak Ridge Electron Linear Accelerator (ORELA) in the years 1970-1990, and from more recent transmission and capture cross section measurements performed at the Geel Linear Accelerator (GELINA). Compared with previous evaluations, the energy range for this resonance analysis was extended from 10 to 20 keV, taking advantage of the high resolution of the most recent ORELA transmission measurements. The experimental database and the method of analysis are described in this report. The neutron transmissions and the capture cross sections calculated with the resonance parameters are compared with the experimental data. A description is given of the statistical properties of the resonance parameters and of the recommended values of the average parameters. The new evaluation results in a slight decrease of the effective capture resonance integral and improves the prediction of integral thermal benchmarks by 70 pcm to 200 pcm.

  12. Estimation of multi-group cross section covariances for {sup 235,238}U, {sup 239}Pu, {sup 241}Am, {sup 56}Fe, {sup 23}Na and {sup 27}Al

    Energy Technology Data Exchange (ETDEWEB)

    De Saint Jean, C.; Archier, P.; Noguere, G.; Litaize, O.; Vaglio-Gaudard, C.; Bernard, D.; Leray, O. [CEA, DEN, DER, Cadarache, F-13108 Saint-Paul-lez-Durance (France)

    2012-07-01

    This paper presents the methodology used to estimate multi-group covariances for some major isotopes used in reactor physics. The starting point of this evaluation is the modelling of the neutron induced reactions based on nuclear reaction models with parameters. These latest are the vectors of uncertainties as they are absorbing uncertainties and correlation arising from the confrontation of nuclear reaction model to microscopic experiment. These uncertainties are then propagated towards multi-group cross sections. As major breakthroughs were then asked by nuclear reactor physicists to assess proper uncertainties to be used in applications, a solution is proposed by the use of integral experiment information at two different stages in the covariance estimation. In this paper, we will explain briefly the treatment of all type of uncertainties, including experimental ones (statistical and systematic) as well as those coming from validation of nuclear data on dedicated integral experiment (nuclear data oriented). We will illustrate the use of this methodology with various isotopes such as {sup 235,238}U, {sup 239}Pu, {sup 241}Am, {sup 56}Fe, {sup 23}Na and {sup 27}Al. (authors)

  13. Accumulation of polonium 210Po, uranium (234U and 238U and plutonium (238Pu and 239+240Pu in tissues and organs of deer Carvidae from northern Poland

    Directory of Open Access Journals (Sweden)

    Strumińska-Parulska D. I.

    2013-04-01

    Full Text Available Livers, kidneys and muscles of large herbivorous animals: roe deer (Capreolus capreolus, red deer (Cervus elaphus and fallow deer (Dama dama, collected in northern Poland, were the subject of the investigation. Polonium, uranium and plutonium activities were measured using alpha spectrometry along with relevant radiochemical procedures. The average concentrations of 210Po ranged between 0.02±0.01 Bq kg−1 ww in muscles and 7.15±0.12 Bq kg−1 ww in kidneys. The concentration of 238U ranged widely between 2.49±0.18 and 69.37±5.45 mBq kg−1 ww. The average concentrations of 239+240Pu ranged between 0.18±0.04 mBq kg−1 ww in muscle and 2.77±0.60 mBq kg−1 ww in kidneys. Statistical analysis showed that the sampling location, sex, age and species did not influence on the radioisotope activities in the analyzed samples.

  14. Cogenetic late Pleistocene rhyolite and cumulate diorites from Augustine Volcano revealed by SIMS 238U-230Th dating of zircon, and implications for silicic magma generation by extraction from mush

    Science.gov (United States)

    Coombs, Michelle L.; Vazquez, Jorge A.

    2014-12-01

    Volcano, a frequently active andesitic island stratocone, erupted a late Pleistocene rhyolite pumice fall that is temporally linked through zircon geochronology to cumulate dioritic blocks brought to the surface in Augustine's 2006 eruption. Zircon from the rhyolite yield a 238U-230Th age of ˜25 ka for their unpolished rims, and their interiors yield a bimodal age populations at ˜26 ka and a minority at ˜41 ka. Zircon from dioritic blocks, ripped from Augustine's shallow magmatic plumbing system and ejected during the 2006 eruption, have interiors defining a ˜26 ka age population that is indistinguishable from that for the rhyolite; unpolished rims on the dioritic zircon are dominantly younger (≤12 ka) indicating subsequent crystallization. Zircon from rhyolite and diorite overlap in U, Hf, Ti, and REE concentrations although diorites also contain a second population of high-U, high temperature grains. Andesites that brought dioritic blocks to the surface in 2006 contain zircon with young (≤9 ka) rims and a scattering of older ages, but few zircon that crystallized during the 26 ka interval. Both the Pleistocene-age rhyolite and the 2006 dioritic inclusions plot along a whole-rock compositional trend distinct from mid-Holocene-present andesites and dacites, and the diorites, rhyolite, and two early Holocene dacites define linear unmixing trends often oblique to the main andesite array and consistent with melt (rhyolite) extraction from a mush (dacites), leaving behind a cumulate amphibole-bearing residue (diorites). Rare zircon antecrysts up to ˜300 ka from all rock types indicate that a Quaternary center has been present longer than preserved surficial deposits.

  15. Energy Dependence of Fission Product Yields from 235U, 238U and 239Pu for Incident Neutron Energies Between 0.5 and 14.8 MeV

    Science.gov (United States)

    Gooden, M. E.; Arnold, C. W.; Becker, J. A.; Bhatia, C.; Bhike, M.; Bond, E. M.; Bredeweg, T. A.; Fallin, B.; Fowler, M. M.; Howell, C. R.; Kelley, J. H.; Krishichayan; Macri, R.; Rusev, G.; Ryan, C.; Sheets, S. A.; Stoyer, M. A.; Tonchev, A. P.; Tornow, W.; Vieira, D. J.; Wilhelmy, J. B.

    2016-01-01

    Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varying degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for 235U, 238U and 239Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed from the dual-fission chamber and gamma

  16. Quantification of {sup 232}Th, {sup 234}U, {sup 235}U and {sup 238}U in river mollusks by magnetic sector mass spectrometry with inductively coupled plasma source (Icp-SFMS); Cuantificacion de {sup 232}Th, {sup 234}U, {sup 235}U y {sup 238}U en moluscos de rios por espectrometria de masas de sector magnetico con fuente de plasma acoplado inductivamente (ICP-SFMS)

    Energy Technology Data Exchange (ETDEWEB)

    Arevalo R, D. L.; Hernandez M, H.; Romero G, E. T.; Lara A, N. [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico); Alfaro de la T, M. C., E-mail: arevalo0591@hotmail.com [Universidad Autonoma de San Luis Potosi, Dr. Salvador Nava s/n, Zona Universitaria, 78290 San Luis Potosi, SLP (Mexico)

    2016-09-15

    The present work deals with the methodology established for the quantification of {sup 232}Th, {sup 234}U, {sup 238}U and {sup 235}U in the shell of gastropod mollusks collected in the rivers Valles, Coy and Axtla of San Luis Potosi, Mexico, which belong to the Panuco River basin; these rivers have as main source of pollution the discharge of municipal sewage, waste from small industries, agricultural and cattle residues and from natural sources. Conventional methods for measuring radio-nuclides are confronted with certain conditions related to the requirement in measurement, basically in the characterization that is related to the concepts of precision and accuracy. The analysis of the gastropod mollusk shell was performed by the Icp-SFMS technique; the main advantages of this technique lie in the isotope quantification capacity, the high precision and the low limits of detection, in this study are very important because these elements are in concentrations between ppb and ppt. This technique allowed the analysis of the samples having a complex matrix by the presence CaCO{sub 3} minimizing the interferences thanks to the ionization efficiency of the Ar plasma. For the species Pachychilus monachus were found concentrations of {sup 232}Th of 0.16-5.37 μg/g and of total U of 0.101-4.081 μg/g being this species where the highest values of total U were found. For Thiara (melanoids) tuberculata the lowest values were found among the different species ({sup 232}Th 0.61-3.61 μg/g and total U 0.006-0.042 μg/g), for Pachychilus suturalis, values of {sup 232}Th of 0.58-6.4 μg/g and for Pachychilus sp. were found between 0.26-7.62 μg/g and for total U values between 0.28-3.33 μg/g. The method offers several advantages: speed, good precision, low values of quantification limits and high sensitivity in the measurement of radio-nuclides and heavy metals. (Author)

  17. Neutrons production in thick targets of Be and {sup 238}U bombarded by 100 MeV/u deuterons and in a thick target of C bombarded by 95 MeV/u {sup 36}Ar. Attenuation in concrete and dose equivalent rate of the activated uranium; Neutrons produits dans des cibles epaisses de Be et {sup 238}U irradiees par des deutons de 100 MeV/u et dans une cible epaisse de C irradiee par des {sup 36}Ar de 95 MeV/u. Longueurs d'attenuation dans du beton et debit d'equivalent de dose resultant de l'activation de l'uranium

    Energy Technology Data Exchange (ETDEWEB)

    Pauwels, N.; Proust, J.; Clapier, F.; Gara, P.; Obert, J. [Paris-11 Univ., 91 - Orsay (France). Inst. de Physique Nucleaire; Mirea, M. [Institute of Physics and Nuclear Engineering, Bucharest (Romania); Belier, G.; Ethvignot, T.; Granier, T. [CEA/DAM-Ile de France, 91 - Bruyeres-Le-Chatel (France). Service de Physique Nucleaire; Liang, C.F. [Paris-11 Univ., 91 - Orsay (France). Centre de Spectrometrie Nucleaire et de Spectrometrie de Masse; Bajard, M.; Leroy, R.; Villari, A.C.C. [Grand Accelerateur National d' Ions Lourds (GANIL), 14 - Caen (France)

    1999-09-01

    Neutrons production in thick targets of Be and {sup 238}U bombarded by 100 MeV/u deuterons and in a thick target of C bombarded by 95 MeV/u {sup 36}Ar. Attenuation in concrete and dose equivalent rate of the activated uranium. The yields of secondary neutrons produced by the interaction of a beam with thick target were determined with activation detectors. Three projectile-target couples have been studied: deuterons (100 MeV/u)+{sup 238}U, deuterons (100 MeV/u)+{sup 9}Be and {sup 36}Ar (95 MeV/u)+{sup 12}C. At 0 deg.. the yields were also measured after a piece of concrete and the corresponding attenuation length evaluated. The dose rate of the uranium target was monitored during several days after the end of the irradiation. (author)

  18. Evaluation of (n,n') scatteriung cross sections from 0. 8 to 2. 5 MeV for higher collective bands of /sup 232/Th and /sup 238/U in ''standard'' (CN + DI) and ''unified'' (Weidenmerller s-matrix) formalisms

    Energy Technology Data Exchange (ETDEWEB)

    Sheldon, E.; Chan, D.W.S.

    1982-01-01

    Angle-integrated cross sections for inelastic scattering of fast neutrons from 0.8 to 2.5 MeV on /sup 232/Th and /sup 238/U, proceeding to higher collective (quadrupole and octupole vibrational) states in the residual nuclei, have been computed in a standard and a unified approach; the resulting excitation functions have been compared with the experimental data of the Lowell group. In all calculations, a consistent set of optical potential and deformation parameters, as derived by Haouat and Lagrange of the Bruyeres group, was used. The standard formalism employed an incoherent sum of compound-nucleus (CN) and coupled-channels direct-interaction (DI) cross section, evaluated with the programs CINDY and KARJUP (Karlsruhe version of JUPITOR) respectively. Provision was made for the effect of level-width fluctuations and for competing neutron exit channels. The results in general compared well with the measured values, but in several instances disagreed significantly with the ENDF/B-V evaluated data. Still better agreement ensued from the use of the unified formalism based upon energy-averaged second moments of transformed S-matrix elements in a statistical approach developed by Weidenmueller at al. and embodied within a new fluctuation program NANCY with coupled channels and competing channels to generate and manipulate the grand ensemble of S-matrix elements. With only the coupling strengths as adjustable parameters, this offers a promising, reliable means of analysis well suited to the interpretation of neutron scattering on deformed actinide nuclei.

  19. Determination of 238u/235u, 236u/238u and uranium concentration in urine using sf-icp-ms and mc-icp-ms: an interlaboratory comparison.

    Science.gov (United States)

    Parrish, Randall R; Thirlwall, Matthew F; Pickford, Chris; Horstwood, Matthew; Gerdes, Axel; Anderson, James; Coggon, David

    2006-02-01

    Accidental exposure to depleted or enriched uranium may occur in a variety of circumstances. There is a need to quantify such exposure, with the possibility that the testing may post-date exposure by months or years. Therefore, it is important to develop a very sensitive test to measure precisely the isotopic composition of uranium in urine at low levels of concentration. The results of an interlaboratory comparison using sector field (SF)-inductively coupled plasma-mass spectrometry (ICP-MS) and multiple collector (MC)-ICP-MS for the measurement of uranium concentration and U/U and U/U isotopic ratios of human urine samples are presented. Three urine samples were verified to contain uranium at 1-5 ng L and shown to have natural uranium isotopic composition. Portions of these urine batches were doped with depleted uranium (DU) containing small quantities of U, and the solutions were split into 100 mL and 400 mL aliquots that were subsequently measured blind by three laboratories. All methods investigated were able to measure accurately U/U with precisions of approximately 0.5% to approximately 4%, but only selected MC-ICP-MS methods were capable of consistently analyzing U/U to reasonable precision at the approximately 20 fg L level of U abundance. Isotope dilution using a U tracer demonstrates the ability to measure concentrations to better than +/-4% with the MC-ICP-MS method, though sample heterogeneity in urine samples was shown to be problematic in some cases. MC-ICP-MS outperformed SF-ICP-MS methods, as was expected. The MC-ICP-MS methodology described is capable of measuring to approximately 1% precision the U/U of any sample of human urine over the entire range of uranium abundance down to <1 ng L, and detecting very small amounts of DU contained therein.

  20. Measurement of 238U muonic x-rays with a germanium detector setup

    Energy Technology Data Exchange (ETDEWEB)

    Esch, Ernst I [Los Alamos National Laboratory; Jason, Andrew [Los Alamos National Laboratory; Miyadera, Haruo [Los Alamos National Laboratory; Hoteling, Nathan J [Los Alamos National Laboratory; Heffner, Robert H [Los Alamos National Laboratory; Adelmann, Andreas [PAUL SCHERRER INSTITUT; Stocki, Trevor [HEALTH CANADA; Mitchell, Lee [NAVAL RESEARCH LAB

    2009-01-01

    In the field of nuclear non-proliferation muon interactions with materials are of great interest. This paper describes an experiment conducted at the Paul Scherrer Institut (PSI) in Switzerland where a muon beam is stopped in a uranium target. The muons produce characteristic muonic x-rays. Muons will penetrate shielding easily and the produced characteristic x-rays can be used for positive isotope identification. Furthermore, the x-rays for uranium isotopes lie in the energy range of 6-7 MeV, which allows them to have an almost optimal mean free path in heavy shielding such as lead or steel. A measurement was conducted at PSI to prove the feasibility of detecting muonic x-rays from a large sample of depleted uranium (several kilograms) with a germanium detector. In this paper, the experimental setup and analysis of the measurement itself is presented.

  1. Measurements of the Prompt Neutron Spectrum of 238U Fission Induced by 5

    Institute of Scientific and Technical Information of China (English)

    1995-01-01

    2.8MeasurementsofthePromptNeutronSpectrumof ̄(238)UFissionInducedby5.4MeVNeutronsLiAnli;BaiXixiang;WangChunrui;GuoHongchaoLiuY...

  2. Semi-empirical Study on Yield Mass Distribution for n+238U Fission

    Institute of Scientific and Technical Information of China (English)

    XU; Yong-mei; LIU; Li-le; SHU; Neng-chuan; CHEN; Yong-jing; LIU; Ting-jin; SUN; Zheng-jun

    2015-01-01

    A semi-empirical model method is developed for calculating the yield mass distributions and energy dependence for neutron-induced 238 fission.The system potential energy is consisting ofthe macro-energy and 2shell corrections,corresponding to the SL,SI and SII fission channels.The yield could be expressed with a five-Gaussianlike formula with 13 parameters,which were

  3. Production of neutron-rich isotopes in {sup 82}Se+{sup 238}U grazing reaction

    Energy Technology Data Exchange (ETDEWEB)

    Marginean, N.; Corradi, L. [INFN, Laboratori Nazionali di Legnaro Padova (Italy); Berghini, S. [National Institute for Physics and Nuclear Engineering, Bucharest (Romania)] (and others)

    2005-07-01

    The reactions at the grazing angle between heavy ions at energies close to the Coulomb barrier are presently considered as a valuable tool for the production of nuclei far from stability, particularly in the neutron-rich area. Recent high mass-resolution experiments demonstrated that one could observe the transfer of up to six proton stripping (-6p) and six neutron pick-up (+6n) channels with cross sections down to {approx}50-100 {mu}b.

  4. Critical dimensions of /sup 235/U aqueous systems containing /sup 238/U or /sup 232/Th (LWBR Development Program)

    Energy Technology Data Exchange (ETDEWEB)

    Jones, L.L. Jr.; Romesburg, H.C.

    1966-09-01

    Criticality data for homogeneous water moderated and reflected systems containing U/sup e/O/sub 2/ and thoria were analyzed to provide data that will be used to establish fuel handling and storage criteria for finely divided mixtures and alloys of U/sup e/O/sub 2/ + ThO/sub 2/. Homogeneous, water reflected and moderated spheres of thoria containing a wide range of U/sup e/O/sub 2/ wt % have been analyzed by four-group diffusion theory utilizing the one-dimensional code WANDA. The fast-group constants were obtained from the MUFT 5 code which weights a 54-group microscopic cross-section set over a spectrum determined by the buckling and material composition and coalesces these into three fast-group constants. The thermal-group constants were obtained with the KATE 1 code using the ''mixed number density'' option. Stearic acid and sugar were compared with water for effectiveness of moderation and reflection. Water proved to be the best moderator thus far, but sugar (at theoretical density) proved to be superior to water as a reflector. (NSA 21: 1543)

  5. 238U, 232Th profiling and U-series isotope analysis of fossil teeth by laser ablation-ICPMS

    Science.gov (United States)

    Eggins, Stephen; Grün, Rainer; Pike, Alistair W. G.; Shelley, Michael; Taylor, Lois

    2003-05-01

    U and Th concentration profiles in fossil hominid and faunal teeth have been measured by laser ablation ICPMS. These profiles record diverse modes of U and Th uptake, particularly within enamel, that can be broadly related to the state of sample preservation. Observed U profiles are in general inconsistent with existing diffusion-adsorption models developed for U-uptake in bone and teeth. Where the models appear applicable, calculated diffusion rates are several orders of magnitude smaller than previous estimates. Laser ablation ICPMS offers a means of rapidly characterizing U and Th distributions in the enamel and dentine components of teeth as a precursor to ESR and U-series dating. In particular, it should allow the identification of teeth (and also bone) samples that have simple U-uptake histories and are amenable to precise dating by time-consuming and expensive Th-U and Pa-U TIMS techniques. We also demonstrated the use of laser ablation ICPMS to measure U-series isotopes in dentine and enamel samples with relatively high U concentrations (>20 ppm). These results, obtained using a quadrupole ICPMS, illustrate significant promise for in situ U-series isotope analysis, particularly when combined with the greater sensitivity and multi-collection capabilities of new sector ICPMS instrumentation. The latter may permit precise isotope ratio measurements on samples containing only a few ppm of U.

  6. Fission Product Yields from 232Th, 238U, and 235U Using 14 MeV Neutrons

    Science.gov (United States)

    Pierson, B. D.; Greenwood, L. R.; Flaska, M.; Pozzi, S. A.

    2017-01-01

    Neutron-induced fission yield studies using deuterium-tritium fusion-produced 14 MeV neutrons have not yet directly measured fission yields from fission products with half-lives on the order of seconds (far from the line of nuclear stability). Fundamental data of this nature are important for improving and validating the current models of the nuclear fission process. Cyclic neutron activation analysis (CNAA) was performed on three actinide targets-thorium-oxide, depleted uranium metal, and highly enriched uranium metal-at the University of Michigan's Neutron Science Laboratory (UM-NSL) using a pneumatic system and Thermo-Scientific D711 accelerator-based fusion neutron generator. This was done to measure the fission yields of short-lived fission products and to examine the differences between the delayed fission product signatures of the three actinides. The measured data were compared against previously published results for 89Kr, -90, and -92 and 138Xe, -139, and -140. The average percent deviation of the measured values from the Evaluated Nuclear Data Files VII.1 (ENDF/B-VII.1) for thorium, depleted-uranium, and highly-enriched uranium were -10.2%, 4.5%, and -12.9%, respectively. In addition to the measurements of the six known fission products, 23 new fission yield measurements from 84As to 146La are presented.

  7. Procedures for determination of 239,240Pu, 241Am, 237Np, 234,238U, 2

    DEFF Research Database (Denmark)

    Chen, Q.J.; Aarkrog, Asker; Nielsen, Sven Poul;

    2001-01-01

    Since 1987, the Department of Nuclear Safety Research, Risø National Laboratory has developed procedures for analysis of low-level amounts of radioactivity in large samples of 200 liters seawater, 10 gram sediment, soil and other environmental materials.These analytical procedures provide high ch...

  8. Determination of relative krypton fission product yields from 14 MeV neutron induced fission of 238U at the National Ignition Facility

    Science.gov (United States)

    Edwards, E. R.; Cassata, W. S.; Velsko, C. A.; Yeamans, C. B.; Shaughnessy, D. A.

    2016-11-01

    Precisely-known fission yield distributions are needed to determine a fissioning isotope and the incident neutron energy in nuclear security applications. 14 MeV neutrons from DT fusion at the National Ignition Facility induce fission in depleted uranium contained in the target assembly hohlraum. The fission yields of Kr isotopes (85m, 87, 88, and 89) are measured relative to the cumulative yield of 88Kr and compared to previously tabulated values. The results from this experiment and England and Rider are in agreement, except for the 85mKr/88Kr ratio, which may be the result of incorrect nuclear data.

  9. Measurement of the 238U Radiative Capture Cross Section with C6D6 at the CERN n_TOF Facility

    CERN Document Server

    Mingrone, F; Altstadt, S; Andrzejewski, J; Audouin, L; Barbagallo, M; Bécares, V; Bečvář, F; Belloni, F; Berthoumieux, E; Billowes, J; Bosnar, D; Brugger, M; Calviani, M; Calviño, F; Cano-Ott, D; Carrapiço, C; Cerutti, F; Chiaveri, E; Chin, M; Colonna, N; Cortés, G; Cortés-Giraldo, M A; Diakaki, M; Domingo-Pardo, C; Duran, I; Dressler, R; Eleftheriadis, C; Ferrari, A; Fraval, K; Ganesan, S; García, A R; Giubrone, G; Gonçalves, I F; González-Romero, E; Griesmayer, E; Guerrero, C; Gunsing, F; Hernández-Prieto, A; Jenkins, D G; Jericha, E; Kadi, Y; Käppeler, F; Karadimos, D; Kivel, N; Koehler, P; Kokkoris, M; Krtička, M; Kroll, J; Lampoudis, C; Langer, C; Leal-Cidoncha, E; Lederer, C; Leeb, H; Leong, L S; Losito, R; Mallick, A; Manousos, A; Marganiec, J; Martínez, T; Mastinu, P F; Mastromarco, M; Mendoza, E; Mengoni, A; Milazzo, P M; Mirea, M; Mondalaers, W; Paradela, C; Pavlik, A; Perkowski, J; Plompen, A; Praena, J; Quesada, J M; Rauscher, T; Reifarth, R; Riego, A; Robles, M S; Rubbia, C; Sabaté-Gilarte, M; Sarmento, R; Saxena, A; Schillebeeckx, P; Schmidt, S; Schumann, D; Tagliente, G; Tain, J L; Tarrío, D; Tassan-Got, L; Tsinganis, A; Valenta, S; Vannini, G; Variale, V; Vaz, P; Ventura, A; Vermeulen, M J; Vlachoudis, V; Vlastou, R; Wallner, A; Ware, T; Weigand, M; Weiß, C; Wright, T; Žugec, P

    2014-01-01

    We present the preliminary results of the U-238(n,gamma) reaction cross section measurement, performed on April 2012 at the CERN n\\_TOF facility using C6D6 scintillation detectors over an energy range from thermal to 1 MeV. The goal of this measurement, which is part of a larger proposal, is to reach an uncertainty of 2\\% in the cross section. The experimental set-up and the methods used to obtain this result are described.

  10. Accurate fast method with high chemical yield for determination of uranium isotopes (234U, 235U, 238U) in granitic samples using alpha spectroscopy

    Science.gov (United States)

    Guirguis, Laila A.; Farag, Nagdy M.; Salim, Adham K.

    2015-03-01

    The present study aims to use the α-spectroscopy at Nuclear Materials Authority (NMA) of Egypt. A radiochemical technique for analysis uranium isotopes was carried out for ten mineralized granitic samples together with the International standards RGU-1 (IAEA) and St4 (NMA). Several steps of sample preparation, radiochemical separation and source preparation were performed before analysis. Uranium was separated from sample matrix with 0.2 M TOPO in cyclohexane as an extracting agent with a chemical yield 98.95% then uranium was purified from lanthanides and actinides present with 0.2 M TOA in xylene as an extracting agent. The pure fraction was electrodeposited on a mirror-polished copper disc from buffer solution (NaHSO4+H2SO4+NH4OH). Rectangle pt-electrode with an anode-cathode distance of 2 cm was used. Current was 900 mA and the electrodeposition time reach up to 120 min. The achieved results show that the chemical yield ranged between 87.9±6.8 and 98±8.6.

  11. Accurate fast method with high chemical yield for determination of uranium isotopes ({sup 234}U, {sup 235}U, {sup 238}U) in granitic samples using alpha spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Guirguis, Laila A., E-mail: lailagurgus@yahoo.com; Farag, Nagdy M.; Salim, Adham K.

    2015-03-21

    The present study aims to use the α-spectroscopy at Nuclear Materials Authority (NMA) of Egypt. A radiochemical technique for analysis uranium isotopes was carried out for ten mineralized granitic samples together with the International standards RGU-1 (IAEA) and St{sub 4} (NMA). Several steps of sample preparation, radiochemical separation and source preparation were performed before analysis. Uranium was separated from sample matrix with 0.2 M TOPO in cyclohexane as an extracting agent with a chemical yield 98.95% then uranium was purified from lanthanides and actinides present with 0.2 M TOA in xylene as an extracting agent. The pure fraction was electrodeposited on a mirror-polished copper disc from buffer solution (NaHSO{sub 4}+H{sub 2}SO{sub 4}+NH{sub 4}OH). Rectangle pt-electrode with an anode-cathode distance of 2 cm was used. Current was 900 mA and the electrodeposition time reach up to 120 min. The achieved results show that the chemical yield ranged between 87.9±6.8 and 98±8.6. - Highlights: • Radiochemical technique for analysis uranium isotopes. • Alpha-particle spectrometry is performed after a radiochemical procedure. • Electrodeposition conditions for preparation of alpha uranium source. • Using {sup 232}U (t{sub 1/2}=70.6a, E{sub α}=5320.24 keV, intensity=69.1%) as an internal tracer makes it a highly reliable technique.

  12. 质子与裂变核238U反应的理论计算%Theoretical Calculations for p+238U Reactions

    Institute of Scientific and Technical Information of China (English)

    于洪伟; 蔡崇海; 赵志祥

    2005-01-01

    利用球型光学模型、耦合道理论、核内级联、激子模型、蒸发模型、带宽度涨落修正的Hauser-Feshbach模型,Bohr-Wheeler裂变理论,对入射能量从阈能到200MeV的p+238U各种反应进行了计算,计算结果和实验符合较好.

  13. High-precision Measurement of the 238U(n,γ) Cross Section with the Total Absorption Calorimeter (TAC) at n_TOF, CERN

    CERN Document Server

    Wright, T; Billowes, J; Ware, T; Cano-Ott, D; Mendoza, E; Massimi, C; Mingrone, F; Gunsing, F; Berthoumieux, E; Lampoudis, C; Altstadt, S; Andrzejewski, J; Audouin, L; Barbagallo, M; Bécares, V; Bečvář, F; Belloni, F; Boccone, V; Bosnar, D; Brugger, M; Calviani, M; Calviño, F; Carrapiço, C; Cerutti, F; Chiaveri, E; Chin, M; Colonna, N; Cortés, G; Cortés-Giraldo, M A; Diakaki, M; Domingo-Pardo, C; Duran, I; Dressler, R; Dzysiuk, N; Eleftheriadis, C; Ferrari, A; Fraval, K; Ganesan, S; García, A R; Gómez-Hornillos, M B; Gonçalves, I F; González-Romero, E; Griesmayer, E; Giubrone, G; Gurusamy, P; Jenkins, D G; Jericha, E; Kadi, Y; Käppeler, F; Karadimos, D; Kivel, N; Koehler, P; Kokkoris, M; Korschinek, G; Krtička, M; Kroll, J; Langer, C; Lederer, C; Leeb, H; Leong, L S; Losito, R; Manousos, A; Marganiec, J; Martínez, T; Mastinu, P F; Mastromarco, M; Meaze, M; Mengoni, A; Milazzo, P M; Mirea, M; Mondelaers, W; Paradela, C; Pavlik, A; Perkowski, J; Pignatari, M; Plompen, A; Praena, J; Quesada, J M; Rauscher, T; Reifarth, R; Riego, A; Roman, F; Rubbia, C; Sarmento, R; Schillebeeckx, P; Schmidt, S; Schumann, D; Tagliente, G; Tain, J L; Tarrío, D; Tassan-Got, L; Tsinganis, A; Valenta, S; Vannini, G; Variale, V; Vaz, P; Ventura, A; Versaci, R; Vermeulen, M J; Vlachoudis, V; Vlastou, R; Wallner, A; Weigand, M; Weiß, C; Žugec, P

    2014-01-01

    The neutron capture cross section of U-238 is fundamental to the design and operation of current reactors and future fast nuclear reactors, and thus must be measured to a high level of accuracy. An experiment has been performed at the CERN n TOF facility using a 4 pi Total Absorption Calorimeter (TAC) to measure the capture cross section in the resolved resonance region between 1 eV and 25 keV. A preliminary analysis of the TAC data is presented with particular emphasis to the experimental background in this energy region of interest.

  14. Influence of soil parameters on the linearity of the soil-to-plant transfer process of {sup 238}U and {sup 226}Ra

    Energy Technology Data Exchange (ETDEWEB)

    Blanco Rodriguez, P.; Vera Tome, F. [Natural Radioactivity Group. Universidad de Extremadura, 06071 Badajoz (Spain); Lozano, J.C. [Laboratorio de Radiactividad Ambiental. Universidad de Salamanca, 37008 Salamanca (Spain)

    2014-07-01

    Transfer from soil to plant is an important input of radionuclides into the food chain. Also, the mobility of radionuclides in soils is enhanced through their passage into the plant compartment. Thus, the soil-to-plant transfer of radionuclides raises the potential human dose. In radiological risk assessment models, this process is usually considered to be an equilibrium process such that the activity concentration in plants is linearly related to the soil concentration through a constant transfer factor (TF). However, the large variability present by measured TF values leads to major uncertainties in the assessment of risks. One possible way to reduce this variability in TF values is to parametrize their determination. This paper presents correlations of TF with the major element concentrations in soils. The findings confirm the major influence of the chemical environment of a soil on the assimilation process. The variability of TF might be greatly reduced if only the labile fraction were considered. Experiments performed with plants (Helianthus annuus L.) growing in a hydroponic medium appear to confirm this suggestion, showing a linear correlation between the plant and the soil solution activity concentrations. Extracting the labile fraction of a real soil is no trivial task, however. A possible operationally definable method is to consider the water-soluble together with the exchangeable fractions of the soil. Studies performed in granitic soils showed that the labile concentration of uranium and radium strongly depended on the soil's textural characteristics. In this sense, a parametrization is proposed of the labile uranium and radium concentration as a function of the soil's granulometric parameters. (authors)

  15. Assessment of (226)Ra, (238)U, (232)Th, (137)Cs and (40)K activities from the northern coastline of Oman Sea (water and sediments).

    Science.gov (United States)

    Darabi-Golestan, F; Hezarkhani, A; Zare, M R

    2017-02-27

    Water and sediment samples were collected from northern coast of Oman Sea covering from Goatr to Hormoz canyon seaport. Water and sediment quality assessment for naturally or anthropogenic radionuclides at Oman Sea as a main strategic golf for trade and transit, is an important issue. Correspondence analysis (CA) by R-mode analysis represents that sigma(T)-temperature-conductivity-O2 parameters are well-correlated with (226)Ra, (232)Th and (40)K. Accordingly Q-mode analysis revealed an indicator samples of ST13W for different radionuclides, ST03W for O2, and simultaneously ST34W-ST21W-ST08W-ST04W for sigma(T) parameters. The CA results overlapped with factor and cluster analysis results that explained 85.8% of total variance of water samples. Descriptive analysis of sediments indicates more significant variation than water samples. The (232)Th and (226)Ra generally showing that ST13D to ST25D sediments that restricted to Pi Bashk coastline are concentrated from (137)Cs and (40)K. By comparison with reference-values from Iran and other parts of the world, they are acceptable with respect to environmental and radioisotope hazards.

  16. Marked disequilibrium between 234Th and 230Th of the 238U natural radioactive decay chain in IAEA reference materials n. 312, 313 and 314.

    Science.gov (United States)

    Colaianni, A; D'Erasmo, G; Pantaleo, A; Schiavulli, L

    2011-02-01

    A new laboratory for the spectroscopy of natural radioactivity with a good energy resolution is presented. It consists of two distinct parts equipped, respectively, the first one with a HpGe γ-ray detector, whose setup has been already completed, and the second one with large area Silicon α-ray detectors and a radiochemical section for thin α-samples preparation, whose setup is yet in progress and will be the argument of a separate work. The γ-ray spectrometer was calibrated by means of IAEA Reference Materials n. 312, 313, 314 and 375. A large difference from the predictions of secular equilibrium emerged between the activities of (234)Th and (230)Th in Materials n. 312, 313 and 314.

  17. Marked disequilibrium between {sup 234}Th and {sup 230}Th of the {sup 238}U natural radioactive decay chain in IAEA reference materials n. 312, 313 and 314

    Energy Technology Data Exchange (ETDEWEB)

    Colaianni, A. [Dipartimento di Geologia e Geofisica dell' Universita di Bari, Via Orabona, 4 - 70125 Bari (Italy); I.N.F.N. Sezione di Bari, Via G. Amendola, 173 - 70126 Bari (Italy); D' Erasmo, G. [Dipartimento Interateneo di Fisica dell' Universita di Bari, Via G. Amendola, 173 - 70126 Bari (Italy); I.N.F.N. Sezione di Bari, Via G. Amendola, 173 - 70126 Bari (Italy); Pantaleo, A., E-mail: pantaleo@ba.infn.i [I.N.F.N. Sezione di Bari, Via G. Amendola, 173 - 70126 Bari (Italy); Schiavulli, L. [Dipartimento Interateneo di Fisica dell' Universita di Bari, Via G. Amendola, 173 - 70126 Bari (Italy); I.N.F.N. Sezione di Bari, Via G. Amendola, 173 - 70126 Bari (Italy)

    2011-02-15

    A new laboratory for the spectroscopy of natural radioactivity with a good energy resolution is presented. It consists of two distinct parts equipped, respectively, the first one with a HpGe {gamma}-ray detector, whose setup has been already completed, and the second one with large area Silicon {alpha}-ray detectors and a radiochemical section for thin {alpha}-samples preparation, whose setup is yet in progress and will be the argument of a separate work. The {gamma}-ray spectrometer was calibrated by means of IAEA Reference Materials n. 312, 313, 314 and 375. A large difference from the predictions of secular equilibrium emerged between the activities of {sup 234}Th and {sup 230}Th in Materials n. 312, 313 and 314.

  18. U-238-U-234-Th-230-Th-232 systematics and the precise measurement of time over the past 500,000 years

    Science.gov (United States)

    Edwards, R. Lawrence; Chen, J. H.; Wasserburg, G. J.

    1987-01-01

    A method is presented for the high-precision measurement of the Th-230 abundance in corals by isotope-dilution mass spectrometry using techniques developed by Chen and Wasserburg (1980, 1981) and Chen et al. (1986). It is shown that 6 x 10 to the 8th atoms of Th-230 can be measured to + or - 30 percent (2 sigma) and 2 x 10 to the 10th atoms of Th-230 to + or - 2 percent. The time over which useful age data on corals can be obtained ranges from a few years to about 500 ky, with the uncertainty in age ranging from 5 y for a 180-y-old coral, to 44 y for a 8294-y-old coral, to 1.1 ky for a 123.1-ky-old coral. Ages were determined with high analytical precision for several corals that grew during high sea-level stands about 120 ky ago, supporting the view that the dominant cause of Pleistocene climate change was Milankovitch forcing.

  19. Reaction mechanisms in 24.3 MeV/nucleon {sup 238}U induced reactions through a comprehensive study of fission

    Energy Technology Data Exchange (ETDEWEB)

    Chbihi, A.; Galin; Guerreau, D.; Lewitowicz, M.; Morjean, M.; Pouthas, J. [Grand Accelerateur National d`Ions Lourds (GANIL), 14 - Caen (France); Piasecki, E.; Kordyasz, A.; Iwanicki, J.; Jastrzebski, J.; Pienkowski, L. [Warsaw Univ. (Poland); Crema, E. [Sao Paulo Univ., SP (Brazil). Inst. de Fisica; Czarnacki, W.; Kisielinski, M.; Tucholski, A. [Soltan Inst. for Nuclear Studies, Otwock-Swierk (Poland); Gatty, B.; Jacquet, D. [Paris-11 Univ., 91 - Orsay (France). Inst. de Physique Nucleaire; Jahnke, U. [Hahn-Meitner-Institut Berlin GmbH (Germany); Muchorowska, M.

    1994-12-31

    Nuclear reaction mechanisms for system characterized by very different asymmetries (U+C, Si, Ni, Au) have been investigated at 24.3 MeV/nucleon, using as observables both the fission products and the neutron multiplicity. It is clearly observed that the fusion process-whatever its completeness- can only occur with rather light target nuclei, indicating the persistence of potential energy effects much above the interaction barrier. (authors). 22 refs., 1 fig.

  20. Comparative study of different analytical methods for the determination of 238U, 234U, 235U, 230Th and 232Th in NORM samples (Southern Catalonia).

    Science.gov (United States)

    Mola, M; Palomo, M; Peñalver, A; Borrull, F; Aguilar, C

    2013-01-01

    Uranium and thorium isotopes from sludge samples taken from an area of influence of a dicalcium phosphate factory, located close to the Ebro River reservoir in Flix, and from mineral raw materials (coal and phosphate) which were deposited in Tarragona Harbour (Catalonia) have been measured. To do that, several procedures to determine these isotopes have been applied and compared in terms of accuracy, precision and total analysis time. In particular, digestion procedures, such as one based on conventional acidic digestion or another based on the use of microwave digestion, have been tested. Moreover, different radiochemical separation procedures have been applied. In this regard, one method based on liquid-liquid extraction using TBP/Xylene and another based on the use of extraction chromatography using UTEVA resins have been compared. Firstly, the different proposed methods were tested by analyzing a phosphogypsum sediment and a moss-soil sample from two different intercomparison exercises. The microwave digestion - UTEVA method provided the best results (recoveries higher than 82% for uranium and thorium isotopes) and was then applied to the NORM samples. The obtained results showed that the higher uranium and thorium activities values were found in phosphate raw material and in the more superficial samples located in sludge sediments next to the dicalcium phosphate factory. Copyright © 2012 Elsevier Ltd. All rights reserved.

  1. Origin and geochemical behavior of uranium in marine sediments. Utilization of the {sup 234}U/{sup 238}U ratio in marine geochemistry; Origine et comportement geochimique de l`uranium dans les sediments marins. Utilisation du rapport ({sup 234}U/{sup 238}U) en geochimie marine

    Energy Technology Data Exchange (ETDEWEB)

    Organo, Catherine [Paris-11 Univ., 91 - Orsay (France)

    1997-01-20

    The first part of this thesis presents the current situation of knowledge of uranium in marine environment. The second part describes the methods of analysis as well as the material support of the study, i.e., the sediments and marine deposits investigated. The third part is dedicated to the study of uranium mobility in marine sediments characterized by detrital terrigenous composition (pelagic clays). This approach allowed quantifying the entering and leaving flux of uranium after the sediment settling and, to discuss, on this basis, the consequences on the uranium oceanic balance. In the third part the origin and behavior of uranium in zones of high surface productivity is studied. The uranium enrichments observed in the hemi-pelagic sediments of the EUMELI (J.G.O.F.S.-France) programme will constitute a material of study adequate for measuring the variations in the {sup 234}U/2{sup 38U} ratio in solid phase, in response to the oxido-reducing characteristics of the sediment. Thus establishing the origin of the trapped uranium has been possible. Also, the nature of the sedimentary phases related to uranium in bio-genetic sediments in the Austral Ocean was determined. Thus a relationship between the variations in the {sup 234}U/{sup 238} and the diagenetic transformations was possible to establish. Finally in the fifth part a study of the behavior of uranium in a polymetallic shell characteristic for deposits of hydrogenized origin 146 refs., 57 figs., 23 tabs.

  2. Distribution of activity concentrations of {sup 238}U and {sup 232}Th in soil samples from Minas Gerais state; Distribuicao das concentracoes de atividade de {sup 238}U e {sup 232}Th em amostras de solo do Estado de Minas Gerais

    Energy Technology Data Exchange (ETDEWEB)

    Peixoto, C.M.; Rodrigues, P.C.H.; Carvalho Filho, C.A.; Feliciano, V.M.D., E-mail: Patricia.fernandes@meioambiente.mg.gov.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil); Fernandes, P.R.M., E-mail: cmp@cdtn.br, E-mail: pchr@cdtn.br, E-mail: cacf@cdtn.br, E-mail: vmfj@cdtn.br [Fundacao Estadual do Meio Ambiente (FEAM), Belo Horizonte, MG (Brazil)

    2016-07-01

    Soil contamination by radionuclides, heavy metal, pesticides, among others, threatens ecosystems and human health. Environmental monitoring bodies and agencies need reference values for these contaminants in order to assess the impacts of anthropogenic activities on soil contamination. Quality Reference Values (QRVs) reflect the natural concentrations of contaminants in soils without anthropic interference and must be regionally established. The aim of this study was the determination of natural concentrations and quality reference values for U and Th in soils from Minas Gerais State, Brazil. A large variation of the natural activity concentration of these radionuclides in soil was observed. The QRV for U was 86.5 Bq kg{sup -1} and 90.81 Bq kg{sup -1} for Th. Statistical analysis showed that the two elements have a positive correlation with the clay and organic matter content in soil, and with the soil orders Ultisol and Inceptisol. Uranium shows a strong correlation with As, Sb, Se and Hg, while Thorium does not show correlation with any of the trace elements. (author)

  3. Influence of neutron halo in the interaction of {sup 6}He nucleus of 35 MeV/nucleon with {sup 197}Au and {sup 238}U; Influence du halo de neutrons dans l`interaction du noyau {sup 6}He de 35 MeV/nucleon avec {sup 197}Au et {sup 238}U

    Energy Technology Data Exchange (ETDEWEB)

    Perier, Yann [Grand Accelerateur National d`Ions Lourds (GANIL), 14 - Caen (France)

    1997-10-27

    In this study, we have attempted to answer some of the questions still open concerning neutron halo nuclei. The interest of the latter lies in their very peculiar structure. The analysis of the kinematical features of the halo nucleus fragments originating from the dissociation following the interaction with a target nucleus is an essential tool for probing this structure. We studied the {sup 6}He + Au, U at 35 A.MeV system with a new method. Simultaneous measurements of the halo nucleus core, the halo neutrons and the excitation energy deposited in the target nucleus assessed with ORION allowed us to obtain information about the formation of the {sup 5}He nucleus and about the partial validity of the sudden approximation at moderate bombarding energy. The study of the core nucleus and neutron angular distributions confirmed that it is difficult to extract information on the internal structure at the halo neutrons from their widths. The halo neutron longitudinal momentum distributions were studied. Their widths were found to increase as the impact parameter decreases. The {sup 4}He - core parallel momentum distributions were also investigated. The widths are weakly dependent on the excitation energy deposited in the target nucleus, but increase with the {sup 4}He emission angle as for the halo neutrons. The ratio between one- and two-neutron stripping cross sections seems to indicate that the two halo neutrons are strongly correlated with a large dineutron component, as ascertained by a calculation in the framework of the Serber model. (author) 84 refs., 98 figs., 17 tabs.

  4. Glomerular filtration rate in patients with gout and factors influencing the rate

    Directory of Open Access Journals (Sweden)

    F M Kudaeva

    2007-09-01

    Zaklyuchenie. Sushchestvuet zavisimost' mezhdu sostoyaniem azotovydelitel'noy funktsii pochek i vozrastom bol'nykh, dlitel'nost'yu i IT podagry. Nalichie AG, IBS, KhSN dostoverno ukhudshaet azotovydelitel'nuyu funktsiyu pochek pri podagre.

  5. Sequential determination of natural ({sup 232}Th, {sup 238}U) and anthropogenic ({sup 137}Cs, {sup 90}Sr, {sup 241}Am, {sup 239+240}Pu) radionuclides in environmental matrix

    Energy Technology Data Exchange (ETDEWEB)

    Michel, H.; Levent, D.; Barci, V.; Barci-Funel, G.; Hurel, C. [Laboratoire de Radiochimie, Sciences Analytiques et Environnement (LRSAE), Universite de Nice Sophia-Antipolis 06108 Nice Cedex (France)

    2008-07-01

    A new sequential method for the determination of both natural (U, Th) and anthropogenic (Sr, Cs, Pu, Am) radionuclides has been developed for application to soil and sediment samples. The procedure was optimised using a reference sediment (IAEA-368) and reference soils (IAEA-375 and IAEA-326). Reference materials were first digested using acids (leaching), 'total' acids on hot plate, and acids in microwave in order to compare the different digestion technique. Then, the separation and purification were made by anion exchange resin and selective extraction chromatography: Transuranic (TRU) and Strontium (SR) resins. Natural and anthropogenic alpha radionuclides were separated by Uranium and Tetravalent Actinide (UTEVA) resin, considering different acid elution medium. Finally, alpha and gamma semiconductor spectrometer and liquid scintillation spectrometer were used to measure radionuclide activities. The results obtained for strontium-90, cesium-137, thorium-232, uranium- 238, plutonium-239+240 and americium-241 isotopes by the proposed method for the reference materials provided excellent agreement with the recommended values and good chemical recoveries. (authors)

  6. Comment on "Radiocarbon Calibration Curve Spanning 0 to 50,000 Years B.P. Based on Paired 230Th/234U/238U and 14C Dates on Pristine Corals" by R.G. Fairbanks, R. A. Mortlock, T.-C. Chiu, L. Cao, A. Kaplan, T. P. Guilderson, T. W. Fairbanks, A. L. Bloom, P

    Energy Technology Data Exchange (ETDEWEB)

    Reimer, P J; Baillie, M L; Bard, E; Beck, J W; Blackwell, P G; Buck, C E; Burr, G S; Edwards, R L; Friedrich, M; Guilderson, T P; Hogg, A G; Hughen, K A; Kromer, B; McCormac, G; Manning, S; Reimer, R W; Southon, J R; Stuiver, M; der Plicht, J v; Weyhenmeyer, C E

    2005-10-02

    Radiocarbon calibration curves are essential for converting radiocarbon dated chronologies to the calendar timescale. Prior to the 1980's numerous differently derived calibration curves based on radiocarbon ages of known age material were in use, resulting in ''apples and oranges'' comparisons between various records (Klein et al., 1982), further complicated by until then unappreciated inter-laboratory variations (International Study Group, 1982). The solution was to produce an internationally-agreed calibration curve based on carefully screened data with updates at 4-6 year intervals (Klein et al., 1982; Stuiver and Reimer, 1986; Stuiver and Reimer, 1993; Stuiver et al., 1998). The IntCal working group has continued this tradition with the active participation of researchers who produced the records that were considered for incorporation into the current, internationally-ratified calibration curves, IntCal04, SHCal04, and Marine04, for Northern Hemisphere terrestrial, Southern Hemisphere terrestrial, and marine samples, respectively (Reimer et al., 2004; Hughen et al., 2004; McCormac et al., 2004). Fairbanks et al. (2005), accompanied by a more technical paper, Chiu et al. (2005), and an introductory comment, Adkins (2005), recently published a ''calibration curve spanning 0-50,000 years''. Fairbanks et al. (2005) and Chiu et al. (2005) have made a significant contribution to the database on which the IntCal04 and Marine04 calibration curves are based. These authors have now taken the further step to derive their own radiocarbon calibration extending to 50,000 cal BP, which they claim is superior to that generated by the IntCal working group. In their papers, these authors are strongly critical of the IntCal calibration efforts for what they claim to be inadequate screening and sample pretreatment methods. While these criticisms may ultimately be helpful in identifying a better set of protocols, we feel that there are also several erroneous and misleading statements made by these authors which require a response by the IntCal working group. Furthermore, we would like to comment on the sample selection criteria, pretreatment methods, and statistical methods utilized by Fairbanks et al. in derivation of their own radiocarbon calibration.

  7. Application of the grey system theory for forecasting the content of238U in soil near a uranium mine exhaust outlet%用灰色系统理论预测某铀矿排风井周边土壤中铀的质量分数

    Institute of Scientific and Technical Information of China (English)

    叶勇军; 丁德馨; 李向阳; 周星火; 刘栋

    2008-01-01

    为预测铀矿排风井周边土壤中铀的质量分数,基于灰色系统的建模、关联度分析和残差辨识理论,建立了常规GM(1,1)预测模型.根据2001-2006年某铀矿排风井周边土壤中铀质量分数的监测数据,证实该模型预测结果与实际监测结果吻合较好,并且预测精度等级较高;同时外推预测了2007年该铀矿排风井周边土壤中铀质量分数,预测结果与实际监测结果的相对误差为4.54%,表明GM(1,1)预测模型具有较高的实用价值,为铀矿排风井周边土壤中铀质量分数的预测提供了一种方便有效的方法.

  8. The Average Lifetime of Giant Composite Systems Formed in Strongly Damped Collisions

    Institute of Scientific and Technical Information of China (English)

    TIAN Jun-Long; WU Xi-Zhen; OU Li; LI Zhu-Xia

    2007-01-01

    The dynamic, adiabatic and diabatic entrance potentials in strongly damped reactions of 238 U+238 U, 232Th+250 Cf are calculated and compared. The feature of the dynamical potential implies that it is possible for the composite systems to stick together for a period of time. By means of the improved quantum molecular dynamics model the time evolution of the density and charge distributions of giant composite systems and their fragments for reactions 238U+238U, 232Th+250Cf are investigated, from which the lifetimes of giant composite systems at different energies are obtained. The longest average lifetime of 238 U+238 U is found when the incident energy is about Ec.m.=1080 Me V, which is about 1200 fm/c.

  9. Lichens and mosses as polonium and uranium biomonitors on Sobieszewo Island.

    Science.gov (United States)

    Boryło, Alicja; Romańczyk, Grzegorz; Skwarzec, Bogdan

    2017-01-01

    In the study the activities of polonium (210)Po and uranium (234)U, (238)U radionuclides in moss and lichen samples were determined using the alpha spectrometry. Different lichens and mosses were collected around the Sobieszewo Island (northern Poland) and investigated for potential use as biomonitors for (210)Po and (238)U deposition. Mosses and lichens have a high efficiency in capturing (210)Po and (238)U from atmospheric fallout. The obtained results showed that (210)Po, (238)U concentrations are changing in analyzed thallophytes samples depending on the type of thallus.

  10. The study of equivalent dose of uranium in long bean (V. U. Sesquipedalis) and the effect on human

    Energy Technology Data Exchange (ETDEWEB)

    Rashid, Nur Shahidah Abdul; Yoshandi, Tengku Mohammad; Majid, Sukiman Sarmania Amran Ab.; Mohamed, Faizal; Siong, Khoo Kok, E-mail: khoo@ukm.edu.my [School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia (UKM), 43600 Bangi, Selangor (Malaysia)

    2016-01-22

    In the case of accidental release of Uranium-238 ({sup 238}U) radionuclides in a nuclear facility or in the environment, internal contamination by either acute or chronic exposure has the potential to induce both radiological and chemical toxic effects. A study was conducted to estimate the {sup 238}U radionuclide concentration in the long beans using Induced Coupled Mass Plasma-Spectrometry (ICP-MS). {sup 238}U radionuclide is a naturally occurring radioactive material that can be found in soil and can be transferred to the long bean (Vigna unguiculata subsp. Sesquapedalis) directly or indirectly via water or air. Kidney and liver are the major sites of deposition of {sup 238}U radionuclide. The obtained dose exposed in the liver and kidney is used to assess the safety level for public intake of {sup 238}U radionuclide from the consumption of long beans. The concentration of {sup 238}U radionuclide measured in long bean samples was 0.0226 ± 0.0009 mg/kg. Total activity of {sup 238}U radionuclide was 0.0044 ± 0.0002 Bq/day with the daily intake of 0.3545 ± 0.0143 µg/day and the annual committed effective dose due to ingestion of {sup 238}U radionuclide in long beans was 0.2230 ± 0.0087 µSv/year. The committed equivalent dose of {sup 238}U radionuclide from the assessment in the liver and kidney are 0.4198 ± 0.0165 nSv and 10.9335 ± 0.4288 nSv. The risk of cancer of {sup 238}U radionuclide was determined to be (86.0466 ± 3.3748) × 10-9. Thus, the results concluded that {sup 238}U radionuclide in local long beans was in the permitted level and safe to consume without posing any significant radiological threat to population.

  11. The study of equivalent dose of uranium in long bean (V. U. Sesquipedalis) and the effect on human

    Science.gov (United States)

    Rashid, Nur Shahidah Abdul; Yoshandi, Tengku Mohammad; Majid, Sukiman Sarmania Amran Ab.; Mohamed, Faizal; Siong, Khoo Kok

    2016-01-01

    In the case of accidental release of Uranium-238 (238U) radionuclides in a nuclear facility or in the environment, internal contamination by either acute or chronic exposure has the potential to induce both radiological and chemical toxic effects. A study was conducted to estimate the 238U radionuclide concentration in the long beans using Induced Coupled Mass Plasma-Spectrometry (ICP-MS). 238U radionuclide is a naturally occurring radioactive material that can be found in soil and can be transferred to the long bean (Vigna unguiculata subsp. Sesquapedalis) directly or indirectly via water or air. Kidney and liver are the major sites of deposition of 238U radionuclide. The obtained dose exposed in the liver and kidney is used to assess the safety level for public intake of 238U radionuclide from the consumption of long beans. The concentration of 238U radionuclide measured in long bean samples was 0.0226 ± 0.0009 mg/kg. Total activity of 238U radionuclide was 0.0044 ± 0.0002 Bq/day with the daily intake of 0.3545 ± 0.0143 µg/day and the annual committed effective dose due to ingestion of 238U radionuclide in long beans was 0.2230 ± 0.0087 µSv/year. The committed equivalent dose of 238U radionuclide from the assessment in the liver and kidney are 0.4198 ± 0.0165 nSv and 10.9335 ± 0.4288 nSv. The risk of cancer of 238U radionuclide was determined to be (86.0466 ± 3.3748) × 10-9. Thus, the results concluded that 238U radionuclide in local long beans was in the permitted level and safe to consume without posing any significant radiological threat to population.

  12. Characterization of elements in marine organisms

    Energy Technology Data Exchange (ETDEWEB)

    Ishii, Toshiaki [National Inst. of Radiological Sciences, Nakaminato, Ibaraki (Japan). Nakaminato Lab. Branch Office

    1994-03-01

    Characterization of elements was carried out to clarify the mechanisms of bioconcentration and the physiological roles of elements in marine organisms. The concentrations of {sup 238}U in fifty-five species of marine organisms were measured by inductively coupled plasma mass spectrometry. The concentrations of {sup 238}U in soft tissues of marine animals ranged from 0.076 to 500ng/g wet wt. Especially, the branchial heart of cephalopod molluscs showed the specific accumulation of {sup 238}U. The concentration factor of the branchial heart of Octopus vulgaris, which indicated the highest value, was calculated to be about 10{sup 3} by comparing it with the concentration of {sup 238}U (3.2 {+-} 0.2ng/ml) in coastal seawater of Japan. The concentrations of {sup 238}U of twenty species of algae ranged from 10 to 3700ng/g dry wt. (author).

  13. Uranium and radium in groundwater and surface water samples in Morocco

    Science.gov (United States)

    Hakam, O. K.; Choukri, A.; Moutia, Z.; Chouak, A.; Cherkaoui, R.; Reyss, J.-L.; Lferde, M.

    2001-06-01

    Activities and activity ratios of uranium and radium isotopes ( 234U, 238U, 226Ra, 228Ra, 234U/ 238U, 226Ra/ 238U, 228Ra/ 226Ra) have been determined for 15 wells, 14 hot springs, 7 cold springs and 11 rivers. Activities of the radium isotopes were measured by ultra gamma spectrometry using a low background and high efficiency well type germanium detector whereas those of uranium were counted in an alpha spectrometer. The minimal, maximal and average values are reported here for each water source. The obtained results show that, unlike well waters, the thermal spring waters present relatively low 238U activities and elevated 226Ra activities and 234U/ 238U activity ratios. Uranium and radium activities are similar to those published for other non polluting regions of the world.

  14. Direct uranium isotope ratio analysis of single micrometer-sized glass particles.

    Science.gov (United States)

    Kappel, Stefanie; Boulyga, Sergei F; Prohaska, Thomas

    2012-11-01

    We present the application of nanosecond laser ablation (LA) coupled to a 'Nu Plasma HR' multi collector inductively coupled plasma mass spectrometer (MC-ICP-MS) for the direct analysis of U isotope ratios in single, 10-20 μm-sized, U-doped glass particles. Method development included studies with respect to (1) external correction of the measured U isotope ratios in glass particles, (2) the applied laser ablation carrier gas (i.e. Ar versus He) and (3) the accurate determination of lower abundant (236)U/(238)U isotope ratios (i.e. 10(-5)). In addition, a data processing procedure was developed for evaluation of transient signals, which is of potential use for routine application of the developed method. We demonstrate that the developed method is reliable and well suited for determining U isotope ratios of individual particles. Analyses of twenty-eight S1 glass particles, measured under optimized conditions, yielded average biases of less than 0.6% from the certified values for (234)U/(238)U and (235)U/(238)U ratios. Experimental results obtained for (236)U/(238)U isotope ratios deviated by less than -2.5% from the certified values. Expanded relative total combined standard uncertainties U(c) (k = 2) of 2.6%, 1.4% and 5.8% were calculated for (234)U/(238)U, (235)U/(238)U and (236)U/(238)U, respectively. Copyright © 2012 Elsevier Ltd. All rights reserved.

  15. Quasifission dynamics and stability of superheavy systems

    CERN Document Server

    Sekizawa, Kazuyuki

    2016-01-01

    Recent experiments revealed intriguing similarities in the $^{64}$Ni+$^{207}$Pb, $^{132}$Xe+$^{208}$Pb, and $^{238}$U+$^{238}$U reactions at energies around the Coulomb barrier. The experimental data indicate that for all systems substantial energy dissipation takes place, in the first stage of the reaction, although the number of transferred nucleons is small. On the other hand, in the second stage, a large number of nucleons are transferred with small friction and small consumption of time. To understand the observed behavior, various reactions were analyzed based on the microscopic time-dependent Hartree-Fock (TDHF) theory. From a systematic analysis for $^{40,48}$Ca+$^{124}$Sn, $^{40}$Ca+$^{208}$Pb, $^{40}$Ar+$^{208}$Pb, $^{58}$Ni+$^{208}$Pb, $^{64}$Ni+$^{238}$U, $^{136}$Xe+ $^{198}$Pt, and $^{238}$U+$^{238}$U reactions, we find that TDHF reproduces well the measured trends. In addition, the Balian-V\\'en\\'eroni variational principle is applied to head-on collisions of $^{238}$U+$^{238}$U, and the variance...

  16. National low-level waste management program radionuclide report series, Volume 15: Uranium-238

    Energy Technology Data Exchange (ETDEWEB)

    Adams, J.P.

    1995-09-01

    This report, Volume 15 of the National Low-Level Waste Management Program Radionuclide Report Series, discusses the radiological and chemical characteristics of uranium-238 ({sup 238}U). The purpose of the National Low-Level Waste Management Program Radionuclide Report Series is to provide information to state representatives and developers of low-level radioactive waste disposal facilities about the radiological, chemical, and physical characteristics of selected radionuclides and their behavior in the waste disposal facility environment. This report also includes discussions about waste types and forms in which {sup 238}U can be found, and {sup 238}U behavior in the environment and in the human body.

  17. Neutron Age Determination in Fast Reactor Materials using the Group Method

    Directory of Open Access Journals (Sweden)

    Kabanova Marina F.

    2016-01-01

    Full Text Available The article deals with the methods of identifying fast neutron age in sodium (Na and uranium-238 (238U; describes the model of advanced and effective fast neutron nuclear reactors (FN, where Na is a coolant while 238U is involved in the fuel cycle in large quantities; justifies the choice of the group method for calculating the neutron age value in the substances mentioned above that can show the accuracy of the used constants for Na and estimate various versions of multilevel description of neutron moderation in 238U – the most powerful resonance absorber of the neutron reactor active zone.

  18. 236U and Its Measurement With Accelerator Mass Spectrometry

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>236U natural occurring isotopic abundance, 236U/238U atom number ratio, is about 10-14. Therefore, 236U is potentially useful as a ‘fingerprint’ for the presence in the environment or nuclear waste of

  19. Neutron-induced cross sections of actinides via the surrogate-reaction method

    Directory of Open Access Journals (Sweden)

    Ducasse Q.

    2013-12-01

    Full Text Available The surrogate-reaction method is an indirect way of determining cross sections for reactions that proceed through a compound nucleus. This technique may enable neutron-induced cross sections to be extracted for short-lived nuclei that otherwise cannot be measured. However, the validity of the surrogate method has to be investigated. In particular, the absence of a compound nucleus formation and the Jπ dependence of the decay probabilities may question the method. In this work we study the reactions 238U(d,p239U, 238U(3He,t238Np, 238U(3He,4He237U as surrogates for neutron-induced reactions on 238U, 237Np and 236U, respectively, for which good quality data exist. The experimental set-up enabled the measurement of fission and gamma-decay probabilities. The first results are hereby presented.

  20. SHRIMP U-Pb dating of detrital zircons in paragneiss from Oki-Dogo Island, western Japan

    National Research Council Canada - National Science Library

    TSUTSUMI, Yukiyasu; YOKOYAMA, Kazumi; HORIE, Kenji; TERADA, Kentaro; HIDAKA, Hiroshi

    2006-01-01

    We obtained the radiometric ages of detrital zircons from two samples of paragneiss from Oki-Dogo Island, Japan, from the 238U/206Pb ratio and isotopic composition of Pb determined using a Sensitive...

  1. SHRIMP U-Pb dating of detrital zircons in paragneiss from Oki-Dogo Island, western Japan

    National Research Council Canada - National Science Library

    TSUTSUMI, Yukiyasu; YOKOYAMA, Kazumi; HORIE, Kenji; TERADA, Kentaro; HIDAKA, Hiroshi

    2006-01-01

      We obtained the radiometric ages of detrital zircons from two samples of paragneiss from Oki-Dogo Island, Japan, from the 238U/206Pb ratio and isotopic composition of Pb determined using a Sensitive...

  2. Study on Removing Micro-neptunium From Milligramme Uranium

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>In the production of radioisotopes and neutron activation analysis, it is very important to know the fast neutron densities, so that the yields of the radioistopes can be estimated. The 238U (n, 2n) 237U reactor

  3. Neutron-induced cross sections of actinides via the surrogate-reaction method

    Directory of Open Access Journals (Sweden)

    Tveten G. M.

    2013-03-01

    Full Text Available The surrogate-reaction method is an indirect way of determining cross sections for reactions that proceed through a compound nucleus. This technique may enable neutron-induced cross sections to be extracted for short-lived nuclei that otherwise cannot be measured. However, the validity of the surrogate method for extracting capture cross sections has to be investigated. In this work we study the reactions 238U(d,p239U, 238U(3He,t238Np, 238U(3He,4He237U as surrogates for neutroninduced reactions on 238U, 237Np and 236U, respectively, for which good quality data exist. The experimental set-up enabled the measurement of fission and gamma-decay probabilities. First results are presented and discussed.

  4. Compilation of multigroup cross-section covariance matrices for several important reactor materials

    Energy Technology Data Exchange (ETDEWEB)

    Drischler, J.D.; Weisbin, C.R.

    1977-10-01

    Multigroup cross-section covariance matrices are presented for fission in /sup 235/U, /sup 238/U, /sup 239/Pu, and /sup 241/Pu; capture in /sup 235/U, /sup 238/U, /sup 239/Pu, /sup 240/Pu, and /sup 241/Pu; fission neutron yield (anti nu) for /sup 235/U, /sup 238/U, /sup 239/Pu, and /sup 240/Pu; elastic scattering for Na and Fe; non-elastic reactions for Na and Fe; first-level inelastic scattering for /sup 238/U; and all reactions provided in the ENDF/B-IV covariance description of N, O, and C. Other data files generated are included for reference but have not yet been tested. The report presents the nultigroup data in six, ten, and fifteen energy group forms corresponding to weighting of the covariance data with fission (GODIVA), LMFBR (ZPR-6/7) and 1/E spectra, respectively.

  5. Isotopic composition of uranium and thorium in crystalline rocks

    Science.gov (United States)

    Rosholt, John N.

    1983-09-01

    The 238U-234U-230Th-232Th system has been investigated in 84 silicic crystalline rocks obtained from drill cores, surface, and near-surface samples in California, Wyoming, Colorado, and Illinois. Results of these analyses displayed on ternary diagrams with apexes for 238U, 234U, and 230Th indicate five predominant geochemical processes that affected uranium in the rock: (1) bulk uranium leaching where 238U and 234U were removed with little or no fractionation; (2) preferential 234U leaching by alpha recoil displacement (234U recoil loss) with lesser 238U loss; (3) 234U recoil loss with little or no 238U loss; (4) uranium assimilation where both 238U and 234U were added with present-day 234U/238U activity ratios varying from 0.8 to 1.2; and (5) addition of 234U and 230Th by daughter emplacement processes (234U + 230Th recoil gain). Evidence for the existence of 234U and 230Th recoil gain in rocks is the most important finding of this investigation. Radioactive disequilibrium occurs in the majority of rocks analyzed where 234U recoil loss is the predominant process associated with incipient weathering; U assimilation and 234U+230Th recoil gain occur under conditions of substantial water penetration along fractures and into weathered zones in the rocks. Relatively unfractured and petrographically fresh rocks from the UPH-3 drill hole in northern Illinois are closest to being in radioactive equilibrium for any suite of rocks included in this study, and they demonstrate that equilibrium during the last 0.5 m.y. can be maintained over a substantial vertical distance where there has been little or no movement of water in the basement rock. The 238U-234U-230Th system can be a sensitive indicator of geologically recent U mobility and rock/water interaction both in petrographically fresh core samples and in `sealed' fracture zones.

  6. Neutron scattering studies in the actinide region

    Energy Technology Data Exchange (ETDEWEB)

    Beghian, L.E.; Kegel, G.H.R.

    1991-08-01

    During the report period we have investigated the following areas: Neutron elastic and inelastic scattering measurements on {sup 14}N, {sup 181}Ta, {sup 232}Th, {sup 238}U and {sup 239}Pu; Prompt fission spectra for {sup 232}Th, {sup 235}U, {sup 238}U and {sup 239}Pu; Theoretical studies of neutron scattering; Neutron filters; New detector systems; and Upgrading of neutron target assembly, data acquisition system, and accelerator/beam-line apparatus.

  7. Neutron scattering studies in the actinide region. Progress report, August 1, 1988--July 31, 1991

    Energy Technology Data Exchange (ETDEWEB)

    Beghian, L.E.; Kegel, G.H.R.

    1991-08-01

    During the report period we have investigated the following areas: Neutron elastic and inelastic scattering measurements on {sup 14}N, {sup 181}Ta, {sup 232}Th, {sup 238}U and {sup 239}Pu; Prompt fission spectra for {sup 232}Th, {sup 235}U, {sup 238}U and {sup 239}Pu; Theoretical studies of neutron scattering; Neutron filters; New detector systems; and Upgrading of neutron target assembly, data acquisition system, and accelerator/beam-line apparatus.

  8. Calorimetric low temperature detectors for low-energetic heavy ions and their application in accelerator mass spectrometry.

    Science.gov (United States)

    Kraft-Bermuth, S; Andrianov, V A; Bleile, A; Echler, A; Egelhof, P; Kiseleva, A; Kiselev, O; Meier, H J; Meier, J P; Shrivastava, A; Weber, M; Golser, R; Kutschera, W; Priller, A; Steier, P; Vockenhuber, C

    2009-10-01

    The energy-sensitive detection of heavy ions with calorimetric low temperature detectors was investigated in the energy range of E=0.1-1 MeV/amu, commonly used for accelerator mass spectrometry (AMS). The detectors used consist of sapphire absorbers and superconducting aluminum transition edge thermometers operated at T approximately 1.5 K. They were irradiated with various ion beams (13C, 197Au, 238U) provided by the VERA tandem accelerator in Vienna, Austria. The relative energy resolution obtained was DeltaE/E=(5-9) x 10(-3), even for the heaviest ions such as 238U. In addition, no evidence for a pulse height defect was observed. This performance allowed for the first time to apply a calorimetric low temperature detector in an AMS experiment. The aim was to precisely determine the isotope ratio of 236U/238U for several samples of natural uranium, 236U being known as a sensitive monitor for neutron fluxes. Replacing a conventionally used detection system at VERA by the calorimetric detector enabled to substantially reduce background from neighboring isotopes and to increase the detection efficiency. Due to the high sensitivity achieved, a value of 236U/238U=6.1 x 10(-12) could be obtained, representing the smallest 236U/238U ratio measured at the time. In addition, we contributed to establishing an improved material standard of 236U/238U, which can be used as a reference for future AMS measurements.

  9. Variations in the uranium isotopic compositions of uranium ores from different types of uranium deposits

    Science.gov (United States)

    Uvarova, Yulia A.; Kyser, T. Kurt; Geagea, Majdi Lahd; Chipley, Don

    2014-12-01

    Variations in 238U/235U and 234U/238U ratios were measured in uranium minerals from a spectrum of uranium deposit types, as well as diagenetic phosphates in uranium-rich basins and peraluminous rhyolites and associated autunite mineralisation from Macusani Meseta, Peru. Mean δ238U values of uranium minerals relative to NBL CRM 112-A are 0.02‰ for metasomatic deposits, 0.16‰ for intrusive, 0.18‰ for calcrete, 0.18‰ for volcanic, 0.29‰ for quartz-pebble conglomerate, 0.29‰ for sandstone-hosted, 0.44‰ for unconformity-type, and 0.56‰ for vein, with a total range in δ238U values from -0.30‰ to 1.52‰. Uranium mineralisation associated with igneous systems, including low-temperature calcretes that are sourced from U-rich minerals in igneous systems, have low δ238U values of ca. 0.1‰, near those of their igneous sources, whereas uranium minerals in basin-hosted deposits have higher and more variable values. High-grade unconformity-related deposits have δ238U values around 0.2‰, whereas lower grade unconformity-type deposits in the Athabasca, Kombolgie and Otish basins have higher δ238U values. The δ234U values for most samples are around 0‰, in secular equilibrium, but some samples have δ234U values much lower or higher than 0‰ associated with addition or removal of 234U during the past 2.5 Ma. These δ238U and δ234U values suggest that there are at least two different mechanisms responsible for 238U/235U and 234U/238U variations. The 234U/238U disequilibria ratios indicate recent fluid interaction with the uranium minerals and preferential migration of 234U. Fractionation between 235U and 238U is a result of nuclear-field effects with enrichment of 238U in the reduced insoluble species (mostly UO2) and 235U in oxidised mobile species as uranyl ion, UO22+, and its complexes. Therefore, isotopic fractionation effects should be reflected in 238U/235U ratios in uranium ore minerals formed either by reduction of uranium to UO2 or chemical

  10. Light-particle emission from the fissioning nuclei sup 1 sup 2 sup 6 Ba, sup 1 sup 8 sup 8 Pt and sup 2 sup 6 sup 6 sup , sup 2 sup 7 sup 2 sup , sup 2 sup 7 sup 8 110: theoretical predictions and experimental results 24.75.+i; 25.85.-w; 25.60.Pj; 25.70.-z; Nuclear reactions 98Mo(28Si ,X) , E=166,187,204 MeV; 107Ag(19F ,X) , E=128,148 MeV; 154Sm(34S ,X) , E=160,203 MeV; 172Yb(16O ,X) , E=138 MeV; 208Pb(58Ni ,X) , (64Ni ,X) , 232Th(40Ca ,X) , 238U(40Ar ,X) , E=66 -186 MeV; Calculated fusion, fission sigma(L) , prefission particle multiplicities; Deduced entrance channel effects; Comparisons with data

    CERN Document Server

    Pomorski, K; Surowiec, A; Kowal, M; Bartel, J; Dietrich, K G; Richert, J; Schmitt, C; Benoit, B; De Goes-Brennard, E; Donadille, L; Badimon, C

    2000-01-01

    We present a comparison of our model treating fission dynamics in conjunction with light-particle ( n,p,alpha ) evaporation with the available experimental data for the nuclei sup 1 sup 2 sup 6 Ba, sup 1 sup 8 sup 8 Pt and three isotopes of the element Z=110 . The dynamics of the symmetric fission process is described through the solution of a classical Langevin equation for a single collective variable characterizing the nuclear deformation along the fission path. A microscopic approach is used to evaluate the emission rates for prefission light particles. Entrance-channel effects are taken into account by generating an initial spin distribution of the compound nucleus formed by the fusion of two deformed nuclei with different relative orientations.

  11. Evaluation of the Homogeneity of the Uranium Isotope Composition of NIST SRM 610/611 by MC-ICP-MS, MC-TIMS, and SIMS

    Directory of Open Access Journals (Sweden)

    Mindy M. Zimmer

    2014-06-01

    Full Text Available As analytical and microanalytical applications employing uranium isotope ratios increase, so does the need for reliable reference materials, particularly in the fields of geochemistry, geochronology, and nuclear forensics. We present working values for uranium isotopic data of NIST 610/611 glass, collected by multicollector inductively-coupled plasma mass spectrometry (MC-ICP-MS, multicollector thermal ionization mass spectrometry (MC-TIMS, and secondary ion mass spectrometry (SIMS. The presence of depleted U, and, in this case, measureable 236U, makes NIST 610/611 an ideal candidate for a uranium isotopic reference material for nuclear materials. We analyzed multiple chips of three different NIST 611 wafers and found no heterogeneity in 234U/238U, 235U/238U, and 236U/238U within or between the wafers, within analytical uncertainty. We determined working values and uncertainties (using a coverage factor of two using data from this study and the literature for the following U isotope ratios: 234U/238U = 9.45 × 10−6 ± 5.0 × 10−8; 235U/238U = 2.38555 × 10−3 ± 4.7 × 10−7; and 236U/238U = 4.314 × 10−5 ± 4.0 × 10−8. SIMS data show 235U/238U is reproducible to within 1% (within analytical uncertainty in a single wafer, at a scale of 25 μm. Multiple studies have demonstrated homogeneity between wafers of NIST 610 and NIST 611, thus the data reported here can be considered representative of NIST 610 as well.

  12. Uranium isotope evidence for temporary ocean oxygenation in the aftermath of the Sturtian Snowball Earth

    Science.gov (United States)

    Lau, Kimberly V.; Macdonald, Francis A.; Maher, Kate; Payne, Jonathan L.

    2017-01-01

    The appearance and radiation of animals are commonly attributed to Neoproterozoic oceanic oxygenation, yet independent geochemical evidence for such an event remains equivocal. Strata deposited between the Sturtian and Marinoan Snowball Earth glaciations (660 to 640 Ma) contain the earliest animal biomarkers and possible body fossils. To quantify the extent of seafloor oxygenation during this critical interval, we present uranium isotope ratios (238U/235U denoted as δ238 U) from limestone of the Taishir Formation in Mongolia through two stratigraphic sections that are separated by ∼75 km within the same depositional basin. Above the Sturtian glacial deposits, through ∼150 m of stratigraphy, δ238 U compositions have a mean value of -0.47‰. This interval is followed by a ∼0.3‰ decrease in δ238 U, coincident with the Taishir negative carbon isotope excursion. Thereafter, δ238 U values remain relatively low until the erosional unconformity at the base of the Marinoan glacial deposits. Using a box model, we show that the best explanation for the higher δ238 U values of the post-Sturtian limestones is extensive-but temporary-oxygenation of the seafloor, and is inconsistent with a scenario involving only increased delivery of uranium to the oceans due to post-Snowball weathering. The decline in δ238 U in overlying strata, coincident with the Taishir negative δ13 C excursion, indicates a subsequent decrease in seafloor oxygenation. The U isotopic data, combined with modeling results, challenge the notion of a simple, unidirectional oxygenation of Neoproterozoic oceans.

  13. A new series of uranium isotope reference materials for investigating the linearity of secondary electron multipliers in isotope mass spectrometry

    Science.gov (United States)

    Richter, S.; Alonso, A.; Aregbe, Y.; Eykens, R.; Kehoe, F.; Kühn, He; Kivel, N.; Verbruggen, A.; Wellum, R.; Taylor, P. D. P.

    2009-04-01

    A new series of gravimetrically prepared uranium isotope reference materials, the so-called IRMM-074 series, with the n(235U)/n(238U) isotope ratio held constant at unity and the n(233U)/n(238U) isotope ratios varying from 1.0 to 10-6 has been prepared and certified. This series is suited for calibration of secondary electron multipliers used widely in isotope mass spectrometry, in particular for techniques such as thermal ionization mass spectrometry (TIMS), inductively coupled plasma mass spectrometry (ICPMS), accelerator mass spectrometry (AMS) and resonance ionization mass spectrometry (RIMS). The new IRMM-074 was prepared as a replacement for the already exhausted IRMM-072 predecessor series. Uranium materials with high isotopic enrichments of 233U, 235U and 238U were purified using identical methods involving separation on anion and cation column followed by a precipitation as peroxide. The oxides were calcined to convert them to U3O8 simultaneously, in an oven installed in a glove-box that provided a controlled low-humidity environment. The oxides of 235U and 238U were weighed and mixed with a mole ratio n(235U)/n(238U) = 1.0 and then dissolved. The 233U oxide was dissolved to form a separate solution with the same concentration and 6rom this primary solution three dilutions were made by weighing. A weighed amount of the n(235U)/n(238U) solution and weighed amounts of the 233U solutions were mixed in various proportions in order to achieve n(233U)/n(238U) isotope ratios varying from 1.0 to 10-6. The methods for the preparation, the mixing and the mixing calculations are described. The expanded uncertainties (coverage factor k = 2) of the certified isotope ratios for the IRMM-074 series are 0.015% for the n(235U)/n(238U) ratio and 0.025% for the n(233U)/n(238U) ratios, which constitutes an improvement compared to those of the predecessor IRMM-072 series. In addition, recent observations regarding the linearity response of secondary electron multipliers (SEMs

  14. Determination of uranium concentration in ground water samples of Northern Greece

    Directory of Open Access Journals (Sweden)

    Pashalidis I.

    2012-04-01

    Full Text Available The activity concentration of 238U and 234U has been determined in groundwater samples of hot springs and deep wells from the region of Northern Greece. The analysis was performed by alpha spectroscopy after pre-concentration and separation of uranium by cation exchange (Chelex 100 resin and finally its electro-deposition on stainless steel discs. The uranium concentration in deep wells and springs varies strongly between 0.15 and 7.66 μg l−1. Generally the springs present higher uranium concentration than the deep wells, except of the Apol-lonia spring, which has shown the lowest value of 0.15 mg l−1. 238U and 234U activity concentration ranged between 1.8–95.3 mBq l−1 and 1.7–160.1 mBq l−1, respectively. The obtained isotopic ratio 234U/238U varies between 0.95 and 1.74 which means that the two isotopes are not in radioactive equilibrium. The highest 234U/238U activity ratio values correspond to the Langada springs, indicating most probably old-type waters. On the other hand, ground waters from wells with relatively low uranium activity concentration and low 234U/238U isotopic ratios, point to the presence of younger waters with a stronger contribution of a local recharge component to the groundwater.

  15. Analogue studies in the alligator rivers region. In-situ measurement of uranium series nuclides with SHRIMP

    Energy Technology Data Exchange (ETDEWEB)

    Nagano, Tetsushi; Yanase, Nobuyuki; Ohnuki, Toshihiko [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Sato, Tsutomu; Isobe, Hiroshi; Williams, I.S.; Zaw, M.; Payne, T.E.; Airey, P.L.

    1999-03-01

    The SHRIMP analyses have been conducted for rock samples from the Koongarra secondary ore deposit to obtain activity ratios of {sup 234}U/{sup 238}U and isotopic ratios of {sup 207}Pb/{sup 206}Pb and {sup 204}Pb/{sup 206}Pb. Target minerals for the analyses were iron minerals and kaolinite, which are the main weathering products in this area. The activity ratios of {sup 234}U/{sup 238}U were obtained based on counts at masses of uranium metal. The {sup 234}U/{sup 238}U activity ratios based on counts of uranium oxides were not appropriate, because count rates of {sup 234}U{sup 16}O were interfered by those of {sup 238}U{sup 12}C molecule. The activity ratios of {sup 234}U/{sup 238}U were approximately unity for crystalline iron nodules. This fact suggested that the mean residence time of uranium within the iron nodules was at least 1 million years. On the other hand, slightly higher values than unity were obtained for kaolinite. Lead isotopes were investigated and a positive relationship was recognized between {sup 207}Pb/{sup 206}Pb and {sup 204}Pb/{sup 206}Pb isotope ratios. (author)

  16. Variation of uranium isotopic composition in soil within the JCO grounds from the 30 September 1999 criticality accident at JCO, Tokai-mura, Japan.

    Science.gov (United States)

    Yamamoto, Masayoshi; Kawabata, Yoshiko; Murata, Yoshimasa; Komura, Kazuhisa

    2002-08-01

    Following the 30 September 1999 criticality accident at JCO, 29 surface and 3 core soil samples were collected inside and outside the JCO grounds to evaluate possible contamination by 235U-enriched uranium (18.8%) being handled at the time of the accident. Uranium (234U, 235U, and 238U) and thorium (228Th, 230Th, and 232Th) isotopes were determined by alpha-spectrometry and ICP-MS after radiochemical separation. Concentrations of 238U and 234U ranged from 11.3 to 63.5 and 11.6 to 360 mBq g(-1), respectively. Higher amounts of 238U and/or 234U were found in the vicinity of the uranium conversion building. The calculated 234U/235U activity ratios ranged from a 1.0 radioactive equilibrium value to an unusually high 5.7 value. Several of the soil samples showed considerably higher 235U/238U atomic ratios (1.06-4.37%) than 0.725% for natural uranium. Based on the assumption that measured U-series nuclides in soil samples taken from the JCO grounds were almost at radioactive equilibrium up to 230Th, excess uranium could be calculated for each sample. The results suggest that the excess uranium in the soils have lower 235U/238U atomic ratios (a few %) than the 18.8% enrichment of the precipitation tank uranium.

  17. Isotope ratio measurement of uranium in safeguards environmental samples by inductively-coupled plasma mass spectrometry (ICP-MS)

    Energy Technology Data Exchange (ETDEWEB)

    Magara, Masaaki; Sakakibara, Takaaki; Kurosawa, Setsumi; Takahashi, Masato; Sakurai, Satoshi; Hanzawa, Yukiko; Esaka, Fumitaka; Watanabe, Kazuo; Usuda, Shigekazu [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2002-04-01

    In order to measure isotope ratio of uranium in safeguards environmental samples with ICP-MS precisely, production of polyatomic ions of IrAr, PtAr and AuAr was measured and mass bias of ICP-MS is investigated by using isotopic standards of uranium and lead. The intensities of IrAr, PtAr and AuAr relative to the atomic ions were found to be 1.8 x 10{sup -6}, 1.6 x 10{sup -5} and 4.1 x 10{sup -5}, respectively. The production of {sup 193}Ir{sup 40}Ar is too small to interfere with the measurement of {sup 233}U, if the concentration of Ir is the same level as that of {sup 233}U. However, there is possibility that the presence of Pt and Au interferes with the measurement of minor isotopes of uranium and {sup 237}Np. On the other hand, the mass biases of {sup 235}U/{sup 238}U and {sup 208}Pb/{sup 206}Pb were measured with the parameter of {sup 238}U{sup 16}O/{sup 238}U. Since unexpected change of the mass bias during measurements causes frequently erroneous results, the monitoring of {sup 238}U{sup 16}O/{sup 238}U is effective for the precise isotope ratio measurement. (author)

  18. Radionuclide concentrations in mussels collected from the southern coast of Bangladesh

    Energy Technology Data Exchange (ETDEWEB)

    Alam, M.N.; Chowdhury, M.I.; Kamal, M.; Ghose, S. E-mail: rtl@globalctg.net; Matin, A.K.M.A.; Ferdousi, G.S.M

    2000-01-01

    Concentrations of {sup 226}Ra, {sup 232}Th, {sup 238}U, {sup 40}K and {sup 137}Cs were determined in whole soft tissues (WST) and shells of groups of different size of marine mussel Perna viridis L. and estuarine mussel Modiolus striatulus H. and water samples which were collected from the southern coast of Bangladesh. Correlation analysis showed that the concentrations of radionuclides vary with mussel size. A positive correlation existed for {sup 238}U and {sup 40}K and a negative one for {sup 232}Th between the radionuclide concentration and mussel size; {sup 232}Th concentrations in WST and shells of the mussels showed an inverse relationship with those of {sup 238}U and {sup 40}K, while {sup 238}U showed positive correlation with {sup 40}K. The concentration factors (CF) for {sup 226}Ra, {sup 232}Th and {sup 238}U in both P. viridis and M. striatulus were higher than those for {sup 40}K. The contents of {sup 137}Cs in both mussels were below the detection limit.

  19. Natural radioactivity measurements in the granite rock of quarry sites, Johor, Malaysia

    Science.gov (United States)

    Alnour, I. A.; Wagiran, H.; Ibrahim, N.; Laili, Z.; Omar, M.; Hamzah, S.; Idi, Bello. Y.

    2012-12-01

    This study was conducted to determine the concentration of natural radionuclides in the granite rocks of selected quarry sites in Johor state, Malaysia and their possible radiological effects. The activity concentrations of 238U, 232Th and 40K in the areas of study indicated varying values of 238U, 232Th and 40K. The highest values of 238U and 232Th concentrations (67±1 and 85±2 Bq kg-1, respectively) were observed at Kamad Quarry (IJM), whereas the highest value of 40K concentration (722±18 Bq kg-1) was detected in Kim Seng Quarry, while the values of activity concentration are lower in Hanson Quarry Products (Kulai) (25±0.5 for 238U, 24±0.5 for 232Th and 429±11 for 40K). Overall, 40K has the highest concentration in the granite rocks of the quarry sites, followed by 232Th and the least for 238U. The radium equivalent activity concentration was found in the range between 94 and 239 Bq kg-1, the absorbed dose rate was found to be in the range between 47 and 112 nGy h-1, and effective dose ranged from 58 to 137 μSv h-1. Moreover, the internal and external hazard index values were given in results lower than unity.

  20. The uranium behaviour during rock-water interaction in the granites from the Itu complex (Sao Paulo, Brazil): a laboratory study

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Helen S.B. da; Marques, Leila S.; Kawauchi, Roberto K., E-mail: leila@iag.usp.br, E-mail: keiji@iag.usp.br [Instituto de Astronomia, Geofisica e Ciencias Atmosfericas. Universidade de Sao Paulo (USP), SP (Brazil)

    2011-07-01

    In order to elucidate the mechanisms involved in the process of uranium leaching due to the rock-water interaction in the granitic rocks from Itu Complex (Sao Paulo, Brazil), an experimental arrangement was developed and built. About 2.5kg of crushed rock fragments from Cabreuva and Indaiatuba Intrusions were maintained at room temperature within a glass flask filled with circulating water. The percolating water was removed periodically (from 10 to 30 days) for uranium analysis and then replaced by an equal volume of fresh water. Alpha spectrometry was used to determine the activity concentrations of {sup 234}U and {sup 238}U, and {sup 234}U/{sup 238}U activity ratios, of the waters as well as of the granites. The results for both samples showed that most of the uranium is leached in the first days after the contact between rock and water. The {sup 234}U/{sup 238}U activity ratios were significantly greater than unity, indicating radioactive disequilibrium between those isotopes, probably due to alpha recoil. Although the uranium activity concentrations in the water samples diminished with the increasing of time, it was not observed considerable variations of the {sup 234}U/{sup 238}U activity ratios. It was also noticed that, the amount of leached uranium as well as the {sup 234}U/{sup 238}U activity ratios are characteristics of each sample submitted to leaching, reflecting the differences of the granite facies mineralogy.(author)

  1. Non-destructive determination of uranium, thorium and 40K in tobacco and their implication on radiation dose levels to the human body.

    Science.gov (United States)

    Landsberger, S; Lara, R; Landsberger, S G

    2015-11-01

    The naturally occurring radionuclides of (235)U, (238)U and (232)Th and their daughter products are a potential major source of anthropogenic radiation to tobacco smokers. Often overlooked is the presence of (40)K in tobacco and its implication to radiation dose accumulation in the human body. In this study, these three radiation sources have been determined in four typical US cigarettes using neutron activation analysis (NAA). The NAA reactions of (238)U(n,γ)(239)U, (232)Th(n,γ)(233)Th and (41)K(n,γ)(42)K were used to determine (235)U, (238)U and (232)Th and (40)K, respectively. The activity of (238)U can easily be determined by epithermal NAA of the (238)U(n,γ)(239)U reaction, and the activity of (235, 234)U can easily be deduced. Using isotopic ratios, the activity due to (40)K was found by the determined concentrations of (41)K (also by epithermal neutrons) in the bulk material. Each gram of total potassium yields 30 Bq of (40)K. The annual effective dose for smokers using 20 cigarettes per day was calculate to be 14.6, 137 and 9 μSv y(-1) for (238,235,) (234)U, (232)Th and (40)K, respectively. These values are significantly lower that the dose received from (210)Po except for (232)Th. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  2. Compendium of energy-dependent sensitivity profiles for the TRX-2 thermal lattice

    Energy Technology Data Exchange (ETDEWEB)

    Tomlinson, E.T.; Lucius, J.L.; Drischler, J.D.

    1978-03-01

    Energy-dependent sensitivity profiles for five responses calculated for the TRX-2 thermal lattice with the ORNL sensitivity code system FORSS are presented here both in graphical form and in SENPRO format. The responses are the multiplication factor, k/sub eff/; the ratio of epithermal-to-thermal captures in /sup 238/U, /sup 28/rho; the ratio of epithermal-to-thermal fissions in /sup 235/U, /sup 25/delta; the ratio of fissions in /sup 238/U to fissions in /sup 235/U, /sup 28/delta; and the ratio of captures in /sup 238/U to fissions in /sup 235/U, CR. A summary table of the total sensitivities is also presented.

  3. Gamma-Ray Measurements of Naturally Occurring Radioactive Materials in Sludge, Scale and Well Cores of the Oil Industry in Southern Iraq

    Directory of Open Access Journals (Sweden)

    Abdul Ridha Hussain SUBBER

    2013-12-01

    Full Text Available Radioactivity of nuclides 238U, 226Ra, 232Th and 40K was measured in soil by γ-ray spectrometry using a NaI (Li detector. A criterion was set in order to analyze sludge samples from oil fields and oil well-cores in southern Basrah, in the Iraq oil fields. More than 3 γ-ray energy peaks were used for the determination of 226Ra and 232Th activity concentrations to obtain results that are more accurate. Relationships between the measured radionuclides were discussed. Radionuclides 238U and 226Ra were found in disequilibrium with ratio of specific activities (238 U/226 Ra less than unity for most of the sludge and core samples. The content of radioactive elements in the sludge, scale and well core is found within the range of other petroleum countries in the region.doi:10.14456/WJST.2014.93

  4. Systematic study of anomalous fragment anisotropies in subbarrier complete fusion—fission reactions

    Institute of Scientific and Technical Information of China (English)

    ZhangHuan-Qiao; LiuZu-Hua; 等

    1997-01-01

    The complete fusion-fission is separated from the transter-induced-fission with the fragment folding angle technique.The cross sections and fragment angular distributions for the complete fusion-fission reactions of 11B+ 238U(237Np),237NP,16O+232Th(238U) and 19F+232Th at near-and sub-barrier energies have been measured.The present fusion and fission standard models can reproduces both the excitation functions and the fragment anisotropies for the systems of 11B+238U(237Np)and 12C+237Np;but fail to explain both the experimental data for the other 3 systems simultaneously,The evidence of the entrance-channel dependence of fission-fragment anisotropies is revealsed by comparison of the 11B+237NP and 16O+232Th data.Based on the observations a new version model of preequilibrium fission is put forward to explain the anomaly.

  5. Natural activity concentrations in bottled drinking water and consequent doses.

    Science.gov (United States)

    Kabadayi, Önder; Gümüs, Hasan

    2012-07-01

    The radioactivity concentrations of nuclides (238)U, (232)Th and (40)K in bottled drinking water from six different manufacturers from Turkey were measured using high-resolution gamma-ray spectrometry. The measurement was done using a coaxial high-purity germanium detector system coupled to Ortec-Dspect jr digital MCA system. The average measured activity concentrations of the nuclides (238)U, (232)Th and (40)K are found to be 0.781, 1.05 and 2.19 Bq l(-1), respectively. The measured activity concentrations have been compared with similar studies from different locations. The annual effective doses for ingestion of radionuclides in the water are found to be 0.0246 mSv for (238)U and 0.169 mSv for (232)Th.

  6. Nuclear energy release from fragmentation

    CERN Document Server

    Li, Cheng; Tsang, M B; Zhang, Feng-Shou

    2015-01-01

    Nuclear energy released by splitting Uranium and Thorium isotopes into two, three, four, up to eight fragments with nearly equal size are studied. We found that the energy released come from equally splitting the $^{235,238}$U and $^{230,232}$Th nuclei into to three fragments is largest. The statistical multifragmentation model is employed to calculate the probability of different breakup channels for the excited nuclei. Weighing the the probability distributions of fragments multiplicity at different excitation energies for the $^{238}$U nucleus, we found that an excitation energy between 1.2 and 2 MeV/u is optimal for the $^{235}$U, $^{238}$U, $^{230}$Th and $^{232}$Th nuclei to release nuclear energy of about 0.7-0.75 MeV/u.

  7. Direct gamma-ray measurement of different radionuclides in the surface water of Suez Canal; Mesure directe du rayonnement gamma emis par divers radionucleides dans les eaux de surface du canal de Suez

    Energy Technology Data Exchange (ETDEWEB)

    Lasheen, Y.F.; El-Zakla, T.; Seliman, A.F.; Abdel-Rassoul, A.A. [Hot Labs. Center, Atomic Energy Authority, Cairo (Egypt)

    2008-04-15

    The radioactivity levels of naturally-occurring {sup 238}U, {sup 232}Th, {sup 226}Ra and {sup 40}K and anthropogenic {sup 137}Cs in surface water from eight locations in the Suez Canal have been assessed by gamma-ray spectrometry. The samples were further characterized by determination of the common cations and anions using ion chromatography. A comparison of {sup 137}Cs radioactivity levels in surface water from the Suez Canal with those of other sea waters is presented. The radioactivity levels of {sup 238}U, {sup 232}Th, {sup 226}Ra and {sup 40}K from sea water are also reported. The effect of total dissolved solids (T.D.S.), chloride, sulphate ion concentrations on the radioactivity levels of {sup 238}U, {sup 232}Th and {sup 226}Ra is discussed. (authors)

  8. Uranium isotopes in carbonate aquifers of arid region setting

    DEFF Research Database (Denmark)

    Alshamsi, Dalal M.; Murad, Ahmed A.; Aldahan, Ala

    2013-01-01

    Groundwater in arid and semiarid regions is vital resource for many uses and therefore information about concentrations of uranium isotopes among other chemical parameters are necessary. In the study presented here, distribution of 238U and 235U in groundwater of four selected locations in the so......Groundwater in arid and semiarid regions is vital resource for many uses and therefore information about concentrations of uranium isotopes among other chemical parameters are necessary. In the study presented here, distribution of 238U and 235U in groundwater of four selected locations...... in the southern Arabian peninsula, namely at two locations within the United Arab Emirates (UAE) and two locations in Oman are discussed. The analyses of the uranium isotopes were performed using ICP-MS and the results indicated a range of concentrations for 235U and 238 U at 3–39 ng L-1 (average: 18 ng L-1...

  9. Monte Carlo simulation of indoor external exposure due to gamma-emitting radionuclides in building materials

    Science.gov (United States)

    Deng, Jun; Cao, Lei; Su, Xu

    2014-10-01

    The use of building materials containing naturally occurring radionuclides, such as 40K, 238U, 232Th and their progeny, could lead to external exposures to the residents of such buildings. In this paper, a set of models are constructed to calculate the specific effective dose rates (the effective dose rate per Bq/kg of 40K, the 238U series, and the 232Th series) imposed on residents by building materials with the MCNPX code. The effect of chemical composition, position concerned in the room and thickness as well as density of material is analyzed. In order to facilitate more precise assessment of indoor external dose due to gamma-emitting radionuclides in building materials, three regressive expressions are proposed and validated by measured data to calculate specific effective rates for 40K. the 238U series and the 232Th series, respectively.

  10. A Lane consistent optical model potential for nucleon scattering on actinide nuclei with extended coupling

    Science.gov (United States)

    Quesada, José Manuel; Capote, Roberto; Soukhovitski, Efrem S.; Chiba, Satoshi

    2016-03-01

    An extension for odd-A actinides of a previously derived dispersive coupledchannel optical model potential (OMP) for 238U and 232Th nuclei is presented. It is used to fit simultaneously all the available experimental databases including neutron strength functions for nucleon scattering on 232Th, 233,235,238U and 239Pu nuclei. Quasi-elastic (p,n) scattering data on 232Th and 238U to the isobaric analogue states of the target nucleus are also used to constrain the isovector part of the optical potential. For even-even (odd) actinides almost all low-lying collective levels below 1 MeV (0.5 MeV) of excitation energy are coupled. OMP parameters show a smooth energy dependence and energy independent geometry.

  11. Dating of weathering profiles by radioactive disequilibria: contribution of the study of authigenic mineral fractions; Datation de profils d`alteration par les desequilibres radioactifs: interet de l`etude des fractions minerales authigenes

    Energy Technology Data Exchange (ETDEWEB)

    Dequincey, O.; Chabaux, F.; Clauer, N.; Liewig, N. [Centre de Geochimie de la Surface (ULP/CNRS), 67 - Strasbourg (France); Muller, J.P. [IRD, Unite de Recherche, Geosciences de l`Environnement tropical, 93 - Bondy (France)

    1999-05-01

    Soil isotopic dating is important for understanding mass transfers related to rick weathering. Here we evaluate a method including TIMS analyses of ({sup 234}U/{sup 238}U) activity ratios on > 0.2 {mu}m fraction of Cameroon laterite. Variations of the ({sup 234}U/{sup 238}U) ratios with depth show significant ({sup 234}U/{sup 238}U) disequilibrium at the bottom of the pedological units, and progressive returns towards secular equilibrium above. These results suggest that U fractionation occurs at the base of the units and that the analysed fractions probably evolve as closed/restricted systems within each unit. From these data, an overall age of 1.5 Ma may be proposed for the development of this laterite. (authors) 24 refs.

  12. Standard practice for alternate actinide calibration for inductively coupled plasma-mass spectrometry

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2004-01-01

    1.1 This practice provides guidance for an alternate linear calibration for the determination of selected actinide isotopes in appropriately prepared aqueous solutions by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS). This alternate calibration is mass bias adjusted using thorium-232 (232Th) and uranium-238 (238U) standards. One of the benefits of this standard practice is the ability to calibrate for the analysis of highly radioactive actinides using calibration standards at much lower specific activities. Environmental laboratories may find this standard practice useful if facilities are not available to handle the highly radioactive standards of the individual actinides of interest. 1.2 The instrument response for a series of determinations of known concentration of 232Th and 238U defines the mass versus response relationship. For each standard concentration, the slope of the line defined by 232Th and 238U is used to derive linear calibration curves for each mass of interest using interference equ...

  13. Anthropogenic 236U in Danish Seawater: Global Fallout versus Reprocessing Discharge

    DEFF Research Database (Denmark)

    Qiao, Jixin; Steier, Peter; Nielsen, Sven Poul

    2017-01-01

    concentrations in Danish seawater are distributed within a relatively narrow range of (3.6-8.2) × 107 atom/L and, to a certain extent, independent of salinity. 236U/238U atomic ratios in Danish seawater are more than 4 times higher than the estimated global fallout value of 1× 10-9. The levels of 236U/238U...... seawater. However, unexpectedly high 236U/238U ratios as well as high 236U concentrations were observed at low-salinity locations of the Baltic Sea. While this feature might be interpreted as a clue for another significant 236U input in the Baltic Sea, it may also be caused by the complexity of water...

  14. Energy Dependence of exotic nuclei production cross sections by photofission reaction in GDR range

    CERN Document Server

    Bhowmick, Debasis; Atta, Debasis; Basu, D N; Chakrabarti, Alok

    2015-01-01

    Photofission of actinides is studied in the region of nuclear excitation energies that covers the entire giant dipole resonance (GDR) region. The mass distributions of $^{238}$U photofission fragments have been explored theoretically for eight different endpoint bremsstrahlung energies from 11.5 MeV to 67.7 MeV which correspond to average photon energy of 9.09 MeV to 15.90 MeV. Among these energies, the 29.1 MeV corresponds to the average photon energy of 13.7$\\pm$0.3 MeV which coincides with GDR peak for $^{238}$U photofission. The integrated yield of $^{238}$U photofission as well as charge distribution of photofission products are calculated and its role in producing nuclei and their neutron-richness is investigated.

  15. Determination of concentrations and isotopic ratio of uranium in groundwaters drawn from two deep wells drilled in granitic rocks belonging to Itu intrusive suite; Determinacao das concentracoes e razoes isotopicas de uranio em aguas subterraneas extraidas de pocos perfurados em rochas da suite intrusiva de Itu (SP)

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Francisca de; Reyes, Erika; Marques, Leila Soares [Sao Paulo Univ., SP (Brazil). Inst. de Astronomia, Geofisica e Ciencias Atmosfericas. Dept. de Geofisica]. E-mail: francisca@iag.usp.br; erika@iag.usp.br; leila@iag.usp.br

    2005-07-01

    This paper presents the first results obtained in the determination of dissolved uranium concentrations and ({sup 234}U/{sup 238}U) activity ratios of groundwaters drawn from two deep wells drilled in granitic rocks belonging to Itu Intrusive Suite, which is located at eastern Sao Paulo State. One of the wells, whose groundwaters have been analyzed, is located in Salto Town, while the other one is located in Itu Town. The groundwater sampling is monthly and begun on September, 2004, in order to investigate possible sazonal variations. The alpha spectrometry technique, associated with isotopic dilution method, has been used for these determinations. The data obtained up to now show that the groundwaters from Salto present uranium concentrations significantly lower ((0.098 {+-} 0.007) - (0.17 {+-} 0.01) ng/g) than those from Itu ((0.22 {+-} 0.02) - (0.31 {+-} 0.02) ng/g). The {sup 234}U and {sup 238}U isotopes of the investigated groundwaters from both wells are in radioactive disequilibrium, with ({sup 234}U/{sup 238}U) activity ratios systematically higher than unity. Although the groundwaters from Salto well are characterized by low {sup 234}U and {sup 238}U specific activities they present higher ({sup 234}U/{sup 238}U) activity ratios than those from Itu. The observed differences on the behavior of uranium concentrations and ({sup 234}U/{sup 238}U) activity ratios in the groundwaters from the two wells are very probably due to the large variety of granitic rocks from Itu Intrusive Suite, which are characterized by distinct uranium abundances. (author)

  16. Simultaneous in-situ determination of U-Pb age and trace elements in zircon by LA-ICP-MS in 20 μm spot size

    Institute of Scientific and Technical Information of China (English)

    LIU XiaoMing; GAO Shan; DIWU ChunRong; YUAN HongLin; HU ZhaoChu

    2007-01-01

    Simultaneous in-situ determination of U-Pb agea and 20 trace elements of three international zircon standards (91500, GJ1 and TEMORA 1) and one laboratory zircon standard (SK10-2) separated from Cenozoic fine-grained gabbro was carried out on quadrupole ICP-MS equipped with 193 nm excimer laser in 20 μm spot size. The weighted mean 208Pb/238U ages of g1500, GJ1 and TEMORA 1 are 1064.4±4.8 Ma (2σ), 603.2±2.4 Ma (2σ) and 418.2±2.4 Ma (2σ), respectively. The relative standard deviations (RSDs) of 206Pb/238U ages (2σ) are less than 2.2% for single measurements and 0.6% for weighted means. The obtained weighted mean 206Pb/238U ages of three atandard zircons agree with the recommended values within 2σσerror. The weighted mean 206Pb/238U age of SK10-2 is 31.42±0.25 Ma (2σ)and the RSDs of 206Pb/238U ages (2σ) are between 2.4% and 5.7% for single measurements and less than 0.8% for weighted mean. The obtained weighted mean 206Pb/238U age is in good agreement with the age obtained by Yuan (2004). Trace element concentrations of NIST612 and NIST614 obtained under the same LA-ICP-MS operating conditions agree with the recommended values within analytical error. The results indicate that it is possible to measure U-Pb age and trace elements aimultaneously by LA-ICP-MS in a small spot size of 20 μm.

  17. Solubility of uranium and thorium from a healing earth in synthetic gut fluids: a case study for use in dose assessments.

    Science.gov (United States)

    Höllriegl, Vera; Li, Wei Bo; Leopold, Karsten; Gerstmann, Udo; Oeh, Uwe

    2010-11-01

    The aim of this case study was to estimate the bioaccessibility of uranium ((238)U) and thorium ((232)Th) from a healing earth by analysing the solubility of these radionuclides in synthetic gastric and intestinal fluids. An easy applicable in vitro test system was used to investigate the fractional mobilization of the soil contaminants being potentially available for absorption under human in vivo conditions. These findings provided the basis for a prospective dose assessment. The solubility experiments were performed using two different in vitro digestion methods. The concentrations of (238)U and (232)Th in the solutions extracted from the soil were measured by inductively coupled plasma mass spectrometry (ICP-MS). The dissolved fractions in the synthetic gastrointestinal fluid ranged in average from 10.3% to 13.8% for (238)U and from 0.3% to 1.6% for (232)Th, respectively, depending on the digestion method. Subsequently, the committed effective doses from intake of (238)U and (232)Th after ingestion of the healing earth during 1 year were evaluated for adult persons. Thereby ingestion dose coefficients calculated as a function of bioaccessibility were used. The dose assessments ranged between 4.3 × 10(-7)-1.9 × 10(-6) Sv y(-1) for (238)U and 5.6 × 10(-7)-3.3 × 10(-6) Sv y(-1) for (232)Th, respectively. On the basis of the assumptions and estimations made, the present work indicates a relatively low radiation risk due to (238)U and (232)Th after internal exposure of the healing earth. Copyright © 2010 Elsevier B.V. All rights reserved.

  18. Uranium series isotopes concentration in sediments at San Marcos and Luis L. Leon reservoirs, Chihuahua, Mexico

    Science.gov (United States)

    Méndez-García, C.; Renteria-Villalobos, M.; García-Tenorio, R.; Montero-Cabrera, M. E.

    2014-07-01

    Spatial and temporal distribution of the radioisotopes concentrations were determined in sediments near the surface and core samples extracted from two reservoirs located in an arid region close to Chihuahua City, Mexico. At San Marcos reservoir one core was studied, while from Luis L. Leon reservoir one core from the entrance and another one close to the wall were investigated. 232Th-series, 238U-series, 40K and 137Cs activity concentrations (AC, Bq kg-1) were determined by gamma spectrometry with a high purity Ge detector. 238U and 234U ACs were obtained by liquid scintillation and alpha spectrometry with a surface barrier detector. Dating of core sediments was performed applying CRS method to 210Pb activities. Results were verified by 137Cs AC. Resulting activity concentrations were compared among corresponding surface and core sediments. High 238U-series AC values were found in sediments from San Marcos reservoir, because this site is located close to the Victorino uranium deposit. Low AC values found in Luis L. Leon reservoir suggest that the uranium present in the source of the Sacramento - Chuviscar Rivers is not transported up to the Conchos River. Activity ratios (AR) 234U/overflow="scroll">238U and 238U/overflow="scroll">226Ra in sediments have values between 0.9-1.2, showing a behavior close to radioactive equilibrium in the entire basin. 232Th/overflow="scroll">238U, 228Ra/overflow="scroll">226Ra ARs are witnesses of the different geological origin of sediments from San Marcos and Luis L. Leon reservoirs.

  19. Determination of 210Pb, 210Po, 226Ra, 228Ra and uranium isotopes in drinking water in order to comply with the requirements of the EU ‘Drinking Water Directive.

    Science.gov (United States)

    Vasile, M; Loots, H; Jacobs, K; Verheyen, L; Sneyers, L; Verrezen, F; Bruggeman, M

    2016-03-01

    The European Union published in 2013 a new Drinking Water Directive with stricter requirements for measuring natural radioactivity. In order to adhere to this, a method for sequential separation of 210Pb, 210Po, 238U and 234U in drinking water was applied using UTEVA® and Sr resins. Polonium-210, 238U and 234U were quantified using alpha-particle spectrometry and 210Pb using liquid scintillation counting. Radium-226 and 228Ra were determined using 3M Empore Radium RAD Disks, and their quantification was done using a Quantulus™ 1220 liquid scintillation counter.

  20. Radioactivity level of the ambient environment of Anren bone-coal power station

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The radioactivity level of the ambient environment of Anren Bonc-coalPower Station (BCPS) was investigated systematically. The γ radiation dose ratelevel in the environment, the content of 238U and 226Ra in the ambient soil and thefarmland in the direction of downwind, the concentrations of 238U, 232Th, 226Ra, 40Kand 222Rn, as well as α potential energy in air, and the concentrations of natural Uand Th in effluent are all higher than the corresponding values of the reference site.The additional annual effective dose equivalent to the residents living in the housesmade of bone-coal cinder brick is 2.7mSv.

  1. Measurement of natural and 137Cs radioactivity concentrations at Izmit Bay (Marmara Sea), Turkey

    Science.gov (United States)

    Öksüz, I.; Güray, R. T.; Özkan, N.; Yalçin, C.; Ergül, H. A.; Aksan, S.

    2016-03-01

    In order to determine the radioactivity level at Izmit Bay Marmara Sea, marine sediment samples were collected from five different locations. The radioactivity concentrations of naturally occurring 238U, 232Th and 40K isotopes and also that of an artificial isotope 137Cs were measured by using gamma-ray spectroscopy. Preliminary results show that the radioactivity concentrations of 238U and 232Th isotopes are lower than the average worldwide values while the radioactivity concentrations of the 40K are higher than the average worldwide value. A small amount of 137Cs contamination, which might be caused by the Chernobyl accident, was also detected.

  2. Analysis of dynamical process with mass distribution of fission fragmentin heavy ion reactions

    Directory of Open Access Journals (Sweden)

    Aritomo Y.

    2010-03-01

    Full Text Available We analyzed experimental data obtained for the mass distribution of fission fragments in the reactions 36S+238U and 30Si+238U at several incident energies, which were performed by the JAEA group. Using the dynamical model with the Langevin equation, we precisely investigate the incident energy dependence of the mass distribution of fission fragments. We also consider the fine structures in the mass distribution of fission fragments caused by the nuclear structure at a low incident energy. It is explained why the mass distribution of fission fragments has different features in the two reactions. The fusion cross sections are also estimated.

  3. In situ Th and U isotope determinations of low-U geological samples using laser ablation single-collector sector-field ICPMS

    Science.gov (United States)

    Mertz-Kraus, R.; Jochum, K. P.; Sharp, W. D.; Stoll, B.; Weis, U.; Andreae, M. O.

    2009-12-01

    In situ spatially resolved U-series dating of geological and biological silicates, phosphates and carbonates (e.g., bone, speleothem, coral, and pedogenic silica and carbonate), facilitates measurement of the rates of natural processes (e.g., precipitation, crystallization) during the past 500,000 years. We present a LA-ICPMS technique for precise and accurate determination of Th and U isotopic ratios applicable to samples with U concentrations as low as 0.4 µg/g. Previously, in situ U-series determinations have been done using multi-collector ICPMS. We use a single-collector sector-field ICPMS connected to a 213 Nd:YAG laser ablation system. Precision and accuracy were determined for different matrices, such as synthetic NIST SRM 612, diverse silicate MPI-DING and USGS reference glasses, 91500 zircon, and a travertine previously analyzed by TIMS.230Th and 234U (~0.00001 to 0.0001 µg/g), required laser tracks up to 1800 µm long, rastering over a 400 x 400 µm square and measurement times of 5 to 25 minutes. We applied corrections for background (tails of 232Th, 235U and 238U peaks on 230Th and 234U (0.1 to 6 cps corresponding to a proportion of 0.3 to 30 % of the measured peak for 232Th and 238U concentrations of 0.003 to 10 µg/g), instrumental mass fractionation (~1 % per atomic mass unit), and differences in element sensitivity of Th and U using the certified values of the reference glasses.230Th/238U and 234U/238U determinations varies between 1.6 and 5 % depending on the extent of peak tailing corrections. We obtained 230Th/238U = 1.65 x 10-5 and 234U/238U = 5.29 x 10-5 for BCR-2G (1.7 µg/g U, 5.9 µg/g Th) which agree within 2 % and 4 %, respectively, with TIMS values (Matthews et al., 2008). For the travertine (2.5 µg/g U, 0.003 µg/g Th) the mean values for four scans (~0.14 mg sample each) are 230Th/238U = 2.47 x 10-5 and 234U/238U = 7.49 x 10-5, within 2 % of TIMS values. Matthews K. et al. (2008), Evaluation of Solid Geologic Reference Materials for

  4. U-series Disequilibria in Continental Arcs: NE Japan Case

    Science.gov (United States)

    Tepley, F. J.; Gill, J. B.; Williams, R. W.

    2005-12-01

    Basalts and andesites from continental arcs typically are close to equilibrium between (238U) and (230Th), and have subdued excesses of 226Ra compared to oceanic arcs (Turner et al., 2003). There is ambiguity whether these and other geochemical features derive from subducted sediment, subcontinental lithosphere, or the crust. We report new 238U-234U-230Th-226Ra data for 20 historical to Holocene samples from Asama in the south of NE Japan to Tarumai in the north. Most straddle the equiline with 4.

  5. Determination of radionuclides in Mytilus galloprovicialis by Alpha And Gamma-Spectroscopy

    Directory of Open Access Journals (Sweden)

    H. FLOROU

    2012-12-01

    Full Text Available The natural radionuclides 238U ,234Th, 40K and the main man-made 137Cs, have been studied in Mytilus galloprovincialis (Lamarck, 1819 sampled in the Thermaikos gulf – North Aegean Sea, considered as a bioindicator for radiological assessment in the Mediterranean. The ratio 234U/238U has also been determined. In terms of 137Cs, the activity concentrations in seawater from the studied area have been measured as well, and the concentration factors of 137Cs in Mytilus galloprovincialis are given as a parameter of the organism response to radioactive pollution.

  6. Hope and Inquietudes in Nucleo-cosmochronology

    CERN Document Server

    Arnould, M

    2001-01-01

    Critical views are presented on some nucleo-cosmochronological questions. Progress has been made recently in the development of the 187Re-187Os cosmochronometry. From this, there is good hope for this clock to become of the highest quality for the nuclear dating of the Universe. The simultaneous observation of Th and U in ultra-metal-poor stars would also be a most interesting prospect. In contrast, a serious inquietude is expressed about the reliability of the chronometric attempts based on the classical 232Th-238U and 235U-238U pairs, as well as on the Th (without U) abundance determinations in ultra-metal poor stars.

  7. Hope and Inquietudes in Nucleocosmochronology

    Science.gov (United States)

    Arnould, M.; Goriely, S.

    Critical views are presented on some nucleo-cosmochronological questions. Progress has been made recently in the development of the 187Re-187Os cosmochronometry. From this, there is good hope for this clock to become of the highest quality for the nuclear dating of the Universe. The simultaneous observation of Th and U in ultra-metal-poor stars would also be a most interesting prospect. In contrast, a serious inquietude is expressed about the reliability of the chronometric attempts based on the classical 232Th-238U and 235U-238U pairs, as well as on the Th (without U) abundance determinations in ultra-metal poor stars.

  8. The ultra-pure Ti for the low background experiments

    Science.gov (United States)

    Chepurnov, Alexander; Nisi, Stefano; di Vacri, Maria Laura; Suvorov, Yury

    2013-08-01

    The constant increase in mass of the cryostats, containment tanks, passive shielding and other mechanical elements of the modern low background detectors put more stringent requirements on their radiopurity levels. In general they have to be ˜1 mBq/kg of 238U/232Th or lower, which means that mass concentration should be manufactory line.

  9. Determination of committed effective doses to skin due to ²³⁸U, ²³²Th and ²²²Rn from the application of various Moroccan black soap (Saboun Beldi) samples by members of the general public.

    Science.gov (United States)

    Misdaq, M A; Outeqablit, K

    2010-12-01

    (238)U, (232)Th, (222)Rn and (220)Rn concentrations were measured inside various Moroccan black soap samples widely used by the Moroccan population in traditional baths (Hammans) by using both CR-39 and LR-115 type II solid state nuclear track detectors. The measured (238)U, (232)Th, (222)Rn and (220)Rn concentrations, respectively, ranged from (3.7 ± 0.2) to (11.7 ± 0.7) mBq kg(-1), (0.11 ± 0.01) to (0.32 ± 0.02) mBq kg(-1), (3.8 ± 0.2) to (11.6 ± 0.6) Bq kg(-1) and (0.10 ± 0.01) to (0.31 ± 0.02) Bq kg(-1) for the Moroccan black soap samples studied. The influence of pollution on the concentrations of these radionuclides inside the considered Moroccan black soap was investigated. A new dosimetric model for evaluating annual committed effective doses due to (238)U, (232)Th and (222)Rn to the skin of different age groups of the Moroccan populations from the application of the black soap samples studied was developed. The maximum total committed effective dose to the skin due to (238)U, (232)Th and (222)Rn from the application of unpolluted black soap samples 20 min per week by the Moroccan populations was found to be equal to (0.88 ± 0.05) μ Sv y(-1) cm(-2).

  10. Estimation of Groundwater Radon in North Carolina Using Land Use Regression and Bayesian Maximum Entropy.

    Science.gov (United States)

    Messier, Kyle P; Campbell, Ted; Bradley, Philip J; Serre, Marc L

    2015-08-18

    Radon ((222)Rn) is a naturally occurring chemically inert, colorless, and odorless radioactive gas produced from the decay of uranium ((238)U), which is ubiquitous in rocks and soils worldwide. Exposure to (222)Rn is likely the second leading cause of lung cancer after cigarette smoking via inhalation; however, exposure through untreated groundwater is also a contributing factor to both inhalation and ingestion routes. A land use regression (LUR) model for groundwater (222)Rn with anisotropic geological and (238)U based explanatory variables is developed, which helps elucidate the factors contributing to elevated (222)Rn across North Carolina. The LUR is also integrated into the Bayesian Maximum Entropy (BME) geostatistical framework to increase accuracy and produce a point-level LUR-BME model of groundwater (222)Rn across North Carolina including prediction uncertainty. The LUR-BME model of groundwater (222)Rn results in a leave-one out cross-validation r(2) of 0.46 (Pearson correlation coefficient = 0.68), effectively predicting within the spatial covariance range. Modeled results of (222)Rn concentrations show variability among intrusive felsic geological formations likely due to average bedrock (238)U defined on the basis of overlying stream-sediment (238)U concentrations that is a widely distributed consistently analyzed point-source data.

  11. Uranium-series constraints on radionuclide transport and groundwater flow at the Nopal I uranium deposit, Sierra Pena Blanca, Mexico.

    Science.gov (United States)

    Goldstein, Steven J; Abdel-Fattah, Amr I; Murrell, Michael T; Dobson, Patrick F; Norman, Deborah E; Amato, Ronald S; Nunn, Andrew J

    2010-03-01

    Uranium-series data for groundwater samples from the Nopal I uranium ore deposit were obtained to place constraints on radionuclide transport and hydrologic processes for a nuclear waste repository located in fractured, unsaturated volcanic tuff. Decreasing uranium concentrations for wells drilled in 2003 are consistent with a simple physical mixing model that indicates that groundwater velocities are low ( approximately 10 m/y). Uranium isotopic constraints, well productivities, and radon systematics also suggest limited groundwater mixing and slow flow in the saturated zone. Uranium isotopic systematics for seepage water collected in the mine adit show a spatial dependence which is consistent with longer water-rock interaction times and higher uranium dissolution inputs at the front adit where the deposit is located. Uranium-series disequilibria measurements for mostly unsaturated zone samples indicate that (230)Th/(238)U activity ratios range from 0.005 to 0.48 and (226)Ra/(238)U activity ratios range from 0.006 to 113. (239)Pu/(238)U mass ratios for the saturated zone are 1000 times lower than the U mobility. Saturated zone mobility decreases in the order (238)U approximately (226)Ra > (230)Th approximately (239)Pu. Radium and thorium appear to have higher mobility in the unsaturated zone based on U-series data from fractures and seepage water near the deposit.

  12. Uranium-series constraints on radionuclide transport and groundwater flow at the Nopal I uranium deposit, Sierra Pena Blanca, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Goldstein, S.J.; Abdel-Fattah, A.I.; Murrell, M.T.; Dobson, P.F.; Norman, D.E.; Amato, R.S.; Nunn, A. J.

    2009-10-01

    Uranium-series data for groundwater samples from the Nopal I uranium ore deposit were obtained to place constraints on radionuclide transport and hydrologic processes for a nuclear waste repository located in fractured, unsaturated volcanic tuff. Decreasing uranium concentrations for wells drilled in 2003 are consistent with a simple physical mixing model that indicates that groundwater velocities are low ({approx}10 m/y). Uranium isotopic constraints, well productivities, and radon systematics also suggest limited groundwater mixing and slow flow in the saturated zone. Uranium isotopic systematics for seepage water collected in the mine adit show a spatial dependence which is consistent with longer water-rock interaction times and higher uranium dissolution inputs at the front adit where the deposit is located. Uranium-series disequilibria measurements for mostly unsaturated zone samples indicate that {sup 230}Th/{sup 238}U activity ratios range from 0.005-0.48 and {sup 226}Ra/{sup 238}U activity ratios range from 0.006-113. {sup 239}Pu/{sup 238}U mass ratios for the saturated zone are <2 x 10{sup -14}, and Pu mobility in the saturated zone is >1000 times lower than the U mobility. Saturated zone mobility decreases in the order {sup 238}U{approx}{sup 226}Ra > {sup 230}Th{approx}{sup 239}Pu. Radium and thorium appear to have higher mobility in the unsaturated zone based on U-series data from fractures and seepage water near the deposit.

  13. Comparison Between Theory Calculation and Experiment Measurement of 238U(n, xnγ)

    Institute of Scientific and Technical Information of China (English)

    WANG; Zhao-hui; LI; Xia; HOU; Long; ZHANG; Jing-shang; CHEN; Guo-chang; SU; Xiao-bin; WANG; Qi; ZHANG; Kai

    2013-01-01

    We have improved the experiment condition,simulated the performance of the new detector system and researched the Angular distribution of secondary gamma ray.The experiment result of 238U(n,xnγ)cross section have been analyzed.Its revised factor has been figured out by simulating and analyzing.A

  14. New ideas in calorimetry

    CERN Document Server

    Botner, O

    1981-01-01

    The hadron calorimeter for the CERN ISR experiment R807 is of the fission compensating type, using /sup 238/U as absorber. The possibility of replacing part of the uranium by more easily accessible material without destroying the good properties of a pure uranium- scintillator calorimeter has been investigated. (0 refs).

  15. Determination of traces of uranium and thorium in titanium and copper used for the construction of the Russian Emission Detector 100 by inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Poteshin, Sergey S; Sysoev, Alexey A; Lagunov, Sergey S; Sereda, Andrei; Sosnovtsev, Valery V; Bolozdynya, Alexander I; Efremenko, Yuriy B

    2015-01-01

    The Russian Emission Detector 100 (RED-100) under construction at the National Research Nuclear University MEPhI (Moscow Engineering Physics Institute) is designed to detect the presently undiscovered effect of coherent neutrino scattering. One of the factors limiting the sensitivity of the detector is the spontaneous decay of uranium and thorium in the detector materials. Radioactive impurities in detector materials at levels of parts per billion can significantly affect the sensitivity. Five random samples of titanium and one of copper from materials used in the construction of the detector were selected for assay. The concentration of (232)Th and (238)U were measured by inductively coupled plasma mass spectrometry (ICP- MS) in solid titanium using both: solutions in acids and direct sampling by laser ablation (LA-ICP-MS). The LA- ICP-MS method allowed us to determine (238)U and (232)Th at subnanogram per gram levels. This method is much faster than ICP-MS with liquid injection. The titanium samples studied have impurities in the range between 1 ng g(-1) and 21 ng g(-1) for (238)U and 3 ng g(-1) and 31 ng g(-1) for (232)Th. In copper we set upper limits of 0.4 ng g(-1) for (238)U and 1 ng g(-1)for (232)Th. The total activity of the cryostat constructed from materials studied was estimated to be 43 Bq.

  16. Progress of China Experimental Fast Reactor in 2011

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    1 Background Fast reactor is the reactor which realized the chain fission with fast neutron.As an optional type of generation Ⅳ reactor,fast reactor has three characters:1) It can change 238U to 239Pu and raise the uranium resource utilization

  17. Radiometric fingerprinting of fluvial sediments in the Rhine-Meuse delta, the Netherlands – a feasibility test

    NARCIS (Netherlands)

    Hebinck, K.; Middelkoop, H.; van Diepen, N.M; van der Graaf, E.R.; de Meijer, R.J.

    2007-01-01

    The deposits of the Rhine and the Meuse in the Netherlands alternate in their delta in a complex way. This paper discusses a method to distinguish the deposits of the Rhine and the Meuse based on the differences in natural radioactivity of (40)K, (238)U and (232)Th, and the effect of the age of the

  18. The effect of pH and time on the extractability and speciation of uranium(VI) sorbed to SiO2.

    Science.gov (United States)

    Ilton, Eugene S; Wang, Zheming; Boily, Jean-François; Qafoku, Odeta; Rosso, Kevin M; Smith, Steven C

    2012-06-19

    The effect of pH and contact time on uranium extractability from quartz surfaces was investigated using either acidic or carbonate (CARB) extraction solutions, time-delayed spikes of different U isotopes ((238)U and (233)U), and liquid helium temperature time-resolved laser-induced fluorescence spectroscopy (TRLFS). Quartz powders were reacted with (238)U(VI) bearing solutions equilibrated with atmospheric CO(2) at pH 6, 7, and 8. After 42 days, the suspensions were spiked with (233)U(VI) and reacted for an additional 7 days. Sorbed U was then extracted with either dilute nitric acid or CARB. For the CARB, but not the acid, extraction there was a systematic decrease in extraction efficiency for both isotopes from pH 6 to 8, which was mimicked by less desorption of (238)U, after the (233)U spike, from pH 6 to 8. The efficiency of (233)U extraction was consistently greater than that of (238)U, indicating a strong temporal component to the strength of U association with the surface that was accentuated with increasing pH. TRLFS revealed a strong correlation between CARB extraction efficiency and sorbed U speciation as a function of pH and time. Collectively, the observations show that aging and pH are critical factors in determining the form and strength of uranium-silica interactions.

  19. Experimental Study Of Terrestrial Electron Anti-neutrinos With Kamland

    CERN Document Server

    Tolich, N R

    2005-01-01

    The analysis presented here uses Kamioka Liquid scintillator Anti-Neutrino Detector (KamLAND) to measure the rate of electron anti-neutrinos, ne&d1;' s , produced from terrestrial 238U and 212Th. 238U and 212Th are thought to be the main heat source driving mantle convection in the Earth, which in turn is responsible for plate tectonics. The total terrestrial 238U and 212Th content has been estimated from Earth models and rock samples from a very small fraction of the Earth. Until now there have been no direct measurements. Since ne&d1;' s have an exceedingly small cross section, they propagate undisturbed in the Earth interior, and their measurement near the Earth surface can be used to gain information on their sources. Based on a total of (2.63 ± 0.19) × 1031 target proton-years (0.506 kton- years), the 90% confidence interval for the total number of terrestrial 238U and 212Th ne&d1;' s detected is 4 to 40. This is consistent with the best models of terrestrial 23...

  20. Uranium Isotope Fractionation during Adsorption, (Co)precipitation, and Biotic Reduction.

    Science.gov (United States)

    Dang, Duc Huy; Novotnik, Breda; Wang, Wei; Georg, R Bastian; Evans, R Douglas

    2016-12-06

    Uranium contamination of surface environments is a problem associated with both U-ore extraction/processing and situations in which groundwater comes into contact with geological formations high in uranium. Apart from the environmental concerns about U contamination, its accumulation and isotope composition have been used in marine sediments as a paleoproxy of the Earth's oxygenation history. Understanding U isotope geochemistry is then essential either to develop sustainable remediation procedures as well as for use in paleotracer applications. We report on parameters controlling U immobilization and U isotope fractionation by adsorption onto Mn/Fe oxides, precipitation with phosphate, and biotic reduction. The light U isotope ((235)U) is preferentially adsorbed on Mn/Fe oxides in an oxic system. When adsorbed onto Mn/Fe oxides, dissolved organic carbon and carbonate are the most efficient ligands limiting U binding resulting in slight differences in U isotope composition (δ(238)U = 0.22 ± 0.06‰) compared to the DOC/DIC-free configuration (δ(238)U = 0.39 ± 0.04‰). Uranium precipitation with phosphate does not induce isotope fractionation. In contrast, during U biotic reduction, the heavy U isotope ((238)U) is accumulated in reduced species (δ(238)U up to -1‰). The different trends of U isotope fractionation in oxic and anoxic environments makes its isotope composition a useful tracer for both environmental and paleogeochemical applications.

  1. Determination of uranium concentration and burn-up of irradiated reactor fuel in contaminated areas in Belarus using uranium isotopic ratios in soil samples

    Energy Technology Data Exchange (ETDEWEB)

    Mironov, V.P.; Matusevich, J.L.; Kudrjashov, V.P.; Ananich, P.I.; Zhuravkov, V.V. [Inst. of Radiobiology, Minsk Univ. (Belarus); Boulyga, S.F. [Inst. of Inorganic Chemistry and Analytical Chemistry, Johannes Gutenberg-Univ. Mainz, Mainz (Germany); Becker, J.S. [Central Div. of Analytical Chemistry, Research Centre Juelich, Juelich (Germany)

    2005-07-01

    An analytical method is described for the estimation of uranium concentrations, of {sup 235}U/{sup 238}U and {sup 236}U/{sup 238}U isotope ratios and burn-up of irradiated reactor uranium in contaminated soil samples by inductively coupled plasma mass spectrometry. Experimental results obtained at 12 sampling sites situated on northern and western radioactive fallout tails 4 to 53 km distant from Chernobyl nuclear power plant (NPP) are presented. Concentrations of irradiated uranium in the upper 0-10 cm soil layers at the investigated sampling sites varied from 2.1 x 10{sup -9}g/g to 2.0 x 10{sup -6}g/g depending mainly on the distance from Chernobyl NPP. A slight variation of the degree of burn-up of spent reactor uranium was revealed by analyzing {sup 235}U/{sup 238}U and {sup 236}U/{sup 238}U isotope ratios and the average value amounted to 9.4{+-}0.3 MWd/(kg U). (orig.)

  2. Dissolved uranium, radium and radon evolution in the Continental Intercalaire aquifer, Algeria and Tunisia.

    Science.gov (United States)

    Elliot, Trevor; Bonotto, Daniel Marcos; Andrews, John Napier

    2014-11-01

    Natural, dissolved (238)U-series radionuclides (U, (226)Ra, (222)Rn) and activity ratios (A.R.s: (234)U/(238)U; (228)Ra/(226)Ra) in Continental Intercalaire (CI) groundwaters and limited samples from the overlying Complexe Terminal (CT) aquifers of Algeria and Tunisia are discussed alongside core measurements for U/Th (and K) in the contexts of radiological water quality, geochemical controls in the aquifer, and water residence times. A redox barrier is characterised downgradient in the Algerian CI for which a trend of increasing (234)U/(238)U A.R.s with decreasing U-contents due to recoil-dominated (234)U solution under reducing conditions allows residence time modelling ∼500 ka for the highest enhanced A.R. = 3.17. Geochemical modelling therefore identifies waters towards the centre of the Grand Erg Oriental basin as palaeowaters in line with reported (14)C and (36)Cl ages. A similar (234)U/(238)U trend is evidenced in a few of the Tunisian CI waters. The paleoage status of these waters is affirmed by both noble gas recharge temperatures and simple modelling of dissolved, radiogenic (4)He-contents both for sampled Algerian and Tunisian CI and CT waters. For the regions studied these waters therefore should be regarded as "fossil" waters and treated effectively as a non-renewable resource.

  3. A certified reference material for radionuclides in the water sample from Irish Sea (IAEA-443)

    DEFF Research Database (Denmark)

    Pham, M.K.; Betti, M.; Povinec, P.P.

    2011-01-01

    A new certified reference material (CRM) for radionuclides in sea water from the Irish sea (IAEA-443) is described and the results of the certification process are presented. Ten radionuclides (3H, 40K, 90Sr, 137Cs, 234U, 235U, 238U, 238Pu, 239+240Pu and 241Am) have been certified, and information...

  4. Radiometric fingerprinting of fluvial sediments in the Rhine-Meuse delta, the Netherlands – a feasibility test

    NARCIS (Netherlands)

    Hebinck, K.; Middelkoop, H.; Diepen, N. van; Graaf, E.R. van der; Meijer, R.J. de

    2007-01-01

    The deposits of the Rhine and the Meuse in the Netherlands alternate in their delta in a complex way. This paper discusses a method todistinguish the deposits of the Rhine and the Meuse based on the differences in natural radioactivity of 40K, 238U and 232Th, and the effect ofthe age of the deposits

  5. Measurement of nuclides of uranium and thorium series of disequilibrium using γ-spectroscopy

    Institute of Scientific and Technical Information of China (English)

    刘广山; 黄奕普; 李静; 叶林

    2002-01-01

    The decay dynamic equations of two daughters were resolved as initial activities of daughters are not zero, and gave calculation formula of activities for measuring uranium and thorium series of disequilibrium using γ-spectroscopy. 238U, 234Th, 226Ra, 222Rn, 228Ra, 228Th, 224Ra, 212pb, 210pb and 40K in two sediment samples were determined as application.

  6. Uptake~of U-and Th-series radionuclides by cerral crops in Upper Egypt

    Institute of Scientific and Technical Information of China (English)

    SHABAN Harb; ROLF Michel

    2009-01-01

    The main aim of this study is to determine the activity concentrations of uranium series and thorium series radionuclide in crops cultivated in Upper Egypt. Fifteen types of cereal crops were collected from local markets and analyzed by γ-ray spectrometry. The mean activity concentrations of the natural radionuclides 238U, 226Ra and 232Thdifferent age groups.

  7. Uranium isotopic fractionation factors during U(VI) reduction by bacterial isolates

    Science.gov (United States)

    Basu, Anirban; Sanford, Robert A.; Johnson, Thomas M.; Lundstrom, Craig C.; Löffler, Frank E.

    2014-07-01

    We experimentally determined the magnitude of uranium isotopic fractionation induced by U(VI) reduction by metal reducing bacterial isolates. Our results indicate that microbial U(VI) reduction induces isotopic fractionation; heavier isotopes (i.e., 238U) partition into the solid U(IV) products. The magnitudes of isotopic fractionation (expressed as ε = 1000‰ * (α-1)) for 238U/235U were 0.68‰ ± 0.05‰ and 0.99‰ ± 0.12‰ for Geobacter sulfurreducens strain PCA and strain IFRC-N, respectively. The ε values for Anaeromyxobacter dehalogenans strain FRC-W, strain FRC-R5, a novel Shewanella isolate, and Desulfitobacterium sp. strain Viet1 were 0.72‰ ± 0.15‰, 0.99‰ ± 0.12‰, 0.96‰ ± 0.16‰ and 0.86‰ ± 0.06‰, respectively. Our results show that the maximum ε values of ∼1.0‰ were obtained with low biomass (∼107 cells/mL) and low electron donor concentrations (∼500 μM). These results provide an initial assessment of 238U/235U shifts induced by microbially-mediated U(VI) reduction, which is needed as 238U/235U data are increasingly applied as redox indicators in various geochemical settings.

  8. Fast-neutron capture cross sections of importance in technological applications. [Review

    Energy Technology Data Exchange (ETDEWEB)

    Poenitz, W. P.

    1979-01-01

    The importance of the capture cross section of the major fertile nuclei, /sup 238/U and /sup 232/Th, leads to the consideration of these data. The /sup 238/U (n,..gamma..) cross section is considered of priority as it is part of the /sup 238/U-/sup 239/Pu cycle. Experimental techniques used in the measurements of these data are considered. Data measured more recently are compared with provisions made for the possible explanations of differing results. It is concluded that the /sup 238/U (n,..gamma..) cross section is known with approx. 5% above 10 keV and fulfills the uncertainty limit for this cross section set to achieve design accuracy for k/sub eff/ and the breeding ratio above 500 keV. Below 500 keV, the present uncertainty falls short of the required 1.5 to 3.0% uncertainty. Specific recommendations are made to resolve existing discrepancies and data uncertainties. 84 references.

  9. SOME ASPECTS OF THE INFLUENCE OF URANIUM EXPLOITATION ON THE ENVIRONMENT

    Directory of Open Access Journals (Sweden)

    Stefan DIMOVSKI

    2012-11-01

    Full Text Available Gamma-ray spectrometric measurements of samples of riverbed sediments and soil samples taken along the valley of a river, which runs very close to a uranium mine retaining dam are performed. The content of 238U, 226Ra, 210 Pb, 232Th, and 40K is analyzed. Up to a distance of about 6 km away from the retaining dam, 238U, 226Ra and 210Pb have high concentrations and the content in the sediments samples is consistently higher than the content in the soil samples. In the same interval are observed considerable fluctuations in the contents related to the swamping of the river. Receding at a greater distance from the retaining dam, the concentration of 238U, 226Ra and 210Pb decreases and has values close to the average ones. A very close correlation is established between the contents of the three radioactive nuclides. Regarding 232Th and 40K, the distribution characteristics along the profile are different in comparison with those of the 238U family members. The performed research contributes to the estimate of the radioactive contamination in a specific area situated in the vicinity of a uranium deposit exploited through underground mining.

  10. Worldwide lead-isotope ratio in bivalves and sediments

    DEFF Research Database (Denmark)

    Larsen, Martin Mørk; Jacobsen, Gitte; Strand, Jakob

    The lead-isotope ratio have been used to assess and identify impact of leaded gasoline, coal combustion and  mineral activities[ref 1] due to the difference in 206Pb (~52%), 207Pb (~24%) and 208Pb (~23%) isotope ratios. The source of these differences is the decaying of the parent isotopes of 238U...

  11. Uranium-Series Disequilibria in the Groundwater of the Shihongtan Sandstone-Hosted Uranium Deposit, NW China

    Directory of Open Access Journals (Sweden)

    Xinjian Peng

    2015-12-01

    Full Text Available Uranium (U concentration and the activities of 238U, 234U, and 230Th were determined for groundwaters, spring waters, and lake water collected from the Shihongtan sandstone-hosted U ore district and in the surrounding area, NW China. The results show that the groundwaters from the oxidizing aquifer with high dissolved oxygen concentration (O2 and oxidation-reduction potential (Eh are enriched in U. The high U concentration of groundwaters may be due to the interaction between these oxidizing groundwaters and U ore bodies, which would result in U that is not in secular equilibrium. Uranium is re-precipitated as uraninite on weathered surfaces and organic material, forming localized ore bodies in the sandstone-hosted aquifer. The 234U/238U, 230Th/234U, and 230Th/238U activity ratios (ARs for most water samples show obvious deviations from secular equilibrium (0.27–2.86, indicating the presence of water-rock/ore interactions during the last 1.7 Ma and probably longer. The 234U/238U AR generally increases with decreasing U concentrations in the groundwaters, suggesting that mixing of two water sources may occur in the aquifer. This is consistent with the fact that most of the U ore bodies in the deposit have a tabular shape originati from mixing between a relatively saline fluid and a more rapidly flowing U-bearing meteoric water.

  12. @u234@@Th scavenging and particle export fluxes from the upper 100 m of the Arabian Sea

    Digital Repository Service at National Institute of Oceanography (India)

    Sarin, M.M.; Rengarajan, R.; Ramaswamy, V.

    for the upper 100 m yields a mean scavenging residence time of ~k30 days and a removal rate of ~k 3400 dpm m@u-2@@ d@u-1@@ for @u234@@Th, from dissolved to particulate phases. The deficiency of total @u234@@Th (dissolved + particulate) relative to @u238@@U...

  13. Measurement of Flow Resistance Coefficient of Sodium Valve in Traveling Wave Reactor

    Institute of Scientific and Technical Information of China (English)

    LV; Ming-yu; WANG; Chong; YU; Hua-jin

    2015-01-01

    Traveling wave reactor(TWR)whose fundamental philosophy is achieving breeding and incineration of 238 U which is in the majority in natural uranium at original location through deepened burnup is a new concept fast reactor.It can effectively enhance utilization rate of uranium resources.TWR has much characteristics,such as

  14. Assessment of the vertical distribution of natural radionuclides in a mineralized uranium area in south-west Spain.

    Science.gov (United States)

    Blanco Rodríguez, P; Vera Tomé, F; Lozano, J C

    2014-01-01

    Low-level alpha spectrometry techniques using semiconductor detectors (PIPS) and liquid scintillation (LKB Quantulus 1220™) were used to determine the activity concentration of (238)U, (234)U, (230)Th, (226)Ra, (232)Th, and (210)Pb in soil samples. The soils were collected from an old disused uranium mine located in southwest Spain. The soils were sampled from areas with different levels of influence from the installation and hence had different levels of contamination. The vertical profiles of the soils (down to 40 cm depth) were studied in order to evaluate the vertical distribution of the natural radionuclides. To determine the origin of these natural radionuclides the Enrichment Factor was used. Also, study of the activity ratios between radionuclides belonging to the same radioactive series allowed us to assess the different types of behaviors of the radionuclides involved. The vertical profiles for the radionuclide members of the (238)U series were different at each sampling point, depending on the level of influence of the installation. However, the profiles of each point were similar for the long-lived radionuclides of the (238)U series ((238)U, (234)U, (230)Th, and (226)Ra). Moreover, a major imbalance was observed between (210)Pb and (226)Ra in the surface layer, due to (222)Rn exhalation and the subsequent surface deposition of (210)Pb. Copyright © 2013 Elsevier Ltd. All rights reserved.

  15. Determination of radionuclide concentration of landfill at Eliozu, Port ...

    African Journals Online (AJOL)

    A survey of the radionuclide concentration from landfill around Eliozu in Port- Harcourt ... 232Th, 238U and 40K. 10 soil and 10 water samples collected from the respective ... This value is lesser than the world-averaged of 55 nGy.h−1for soil.

  16. Radioactiviteit van fosfaaterts en fosforslakken van Hoechst te Vlissingen

    NARCIS (Netherlands)

    Mattern; F.C.M.

    1984-01-01

    Uit de onderzoeksresultaten blijkt dat de activiteitsconcentraties aan 238-U en 226-Ra zowel in fosfaaterts als in de daaruit bereide pellets en in de fosforslak vrijwel gelijk zijn en liggen tussen de 1,1 en 1,5 kBq/kg. In het erts zijn 210-Pb en 210-Po vrijwel in evenwicht met het 226-Ra. In

  17. THERMOLUMINESCENT DOSIMETRY

    African Journals Online (AJOL)

    2005-10-20

    Oct 20, 2005 ... abo area of the city has the least radiation dose rate while Obantoku area has the upper limit. aking this as ... 'n Abeokuta. eywords: Environmental radiation, thermoluminescent dosimetry, Abeokuta, outdoor ... Both 238U and 232Th have long decay series with ... effects of radiation exposure (Hanson and.

  18. THERMOLUMINESCENT DOSIMETRY

    African Journals Online (AJOL)

    2005-10-20

    Oct 20, 2005 ... abo area of the city has the least radiation dose rate while Obantoku area has the upper limit. aking this as ... “n Abeokuta. eywords: Environmental radiation, thermoluminescent dosimetry, Abeokuta, outdoor ... Both 238U and 232Th have long decay series with ... effects of radiation exposure (Hanson and.

  19. Implications for soil environment from uranium isotopes of stalagmites

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    By analyzing U and Th isotopic compositions of 41 samples in two stalagmites from Hulu Cave, Nanjing, we first discovered that variations of 238U and d 234U0 along the stalagmite growth-sequence (covering a period from 75 to 18 kaBP) are in high similarity to summer insolation curve at 33°N and d 18O-based climate record of the studied stalagmites. The concentration of 238U is mainly controlled by content of organic matter in the soil above the cave. This mechanism can be used to explain our result that 238U curve of stalagmites is in phase with fluctuation of the d 18O record of the same stalagmites and summer insolation at cave locality. However, 238U concentration curve vs. age is, in amplitude, inconsistent with the climatic curves, possibly due to complex processes of soil-water-rock interaction. d 234U0 indicates pedogenic intensity of soil profile above the cave and sensitively reflects alternations of pedogenesis and aeolian accumulation processes of Xiashu loess in Nanjing. Consequently, uranium concentration and its isotope ratio in stalagmites may provide a new proxy for climate change.

  20. Natural Radiation in byproducts of the production of phosphoric acid; Radiacao natural em residuos gerados no processo de producao de acido fosforico

    Energy Technology Data Exchange (ETDEWEB)

    Silveira, Marcilei A. Guazzelli da; Cardoso, L.L., E-mail: marcilei@fei.edu.br [Centro Universitario da FEI, Sao Bernardo do Campo, SP (Brazil); Medina, N.H. [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil). Institutlo de Fisica

    2014-07-01

    Natural radiation is the largest source of radiation exposure to which man is subject. It is formed basically by cosmic radiation and the radionuclides present in the Earth crust, as {sup 40}K and the elements of the decay series of {sup 232}Th and {sup 238}U. Phosphate ores, which constitutes the raw material for the production of phosphoric acid, have a high rate of natural radiation from the decay series of {sup 232}Th and {sup 238}U. Phosphogypsum, which is naturally radioactivity, is a by-product of the production of phosphoric acid by the wet method. For each ton of phosphoric acid it is produced about 4.5 tons of phosphogypsum. This work presents the analysis of samples collected in all stages of the manufacturing process of phosphoric acid, which generates the phosphogypsum. Gamma-ray spectrometry was used to measure the concentration of the elements of the decay series of {sup 232}Th and {sup 238}U. All analyzed samples showed a high concentration of radionuclides, promoting the need for further steps in the process in order to reduce the presence of such radionuclides in the phosphogypsum. The results indicate the radionuclide {sup 238}U has higher contribution in some samples of the intermediate stages of the process. All samples exceeded the international average range of human exposure to terrestrial gamma radiation, which is 0.3 to 1.0 mSv/year. (author)

  1. Isotope tracer studies of diffusion in silicates and of geological transport processes using actinide elements. Progress report

    Energy Technology Data Exchange (ETDEWEB)

    Wasserburg, G.J.

    1992-12-31

    The following are reported: high abundance sensitivity mass spectrometer for U-Th studies; {sup 238}U-{sup 230}Th disequilibrium in recent lavas from Iceland; water-rock interaction from U-Th studies; resonance ionization mass spectrometry of Os and Ti isotopes; and self-diffusion of Mg.

  2. Determination of the isotopic composition of natural and slightly enriched uranium by alpha-spectrometry

    DEFF Research Database (Denmark)

    Kunzendorf, Helmar

    1968-01-01

    Determinations of the isotope contents of 238U, 235U and 234U in five uranium samples containing 0–5 at% 235U were carried out on the basis of a least-squares fit of the α-spectra from the samples, measured with a semiconductor detector, to the theoretically expected α-spectra. With a simple source...

  3. A simple functional form for proton-nucleus total reaction cross sections

    CERN Document Server

    Amos, K A

    2002-01-01

    A simple functional form has been found that gives a good representation of the total reaction cross sections for the scattering of protons from (15) nuclei spanning the mass range ${}^{9}$Be to ${}^{238}$U and for proton energies ranging from 20 to 300 MeV.

  4. Evaluation of naturally occurring radioactivity across the State of Kuwait using high-resolution gamma-ray spectrometry

    Science.gov (United States)

    Bajoga, A. D.; Alazemi, N.; Shams, H.; Regan, P. H.; Bradley, D. A.

    2017-08-01

    A study of natural radioactivity from 90 different soil samples from the state of Kuwait has been carried out to ascertain the NORM concentration values across the country. The calculated activity concentrations were determined from: (i) the decays of the 226Ra, 214Pb and 214Bi members of the 4n+2 decay chain headed by 238U and; (ii) the 228Ac, 212Pb and 208Tl members of the 4n chain headed by 232Th. The study also included evaluations for the 235U decay chain with the 186 keV doublet transition used together with the measured 4n+2 activity concentration values to determine the 235U/238U isotopic ratios for each sample. The values for the arithmetic mean activity concentrations for 90 separate locations across Kuwait as determined in the current work were 17.2, 14.1, and 368 Bq/kg, with standard deviations of 5.2, 3.7 and 90 Bq/kg for the 238U, 232Th and 40K activity concentrations respectively. Measured isotope ratios for 235U/238U give an arithmetic mean value for all of the samples of 0.045±0.003, consistent with that expected for natural uranium. These results indicate no evidence for a radiologically significant dispersion of additional depleted uranium across the entire State of Kuwait from the 1991 Gulf War.

  5. Uranium series disequilibrium in the coastal surface sediments and sea water of the Arabian sea

    Digital Repository Service at National Institute of Oceanography (India)

    Joshi, L.U.; Zingde, M.D.

    isotopes without attacking the mineral core of the sediment particle. The activity ratios of sup(234) U/ sup(238) U are in the range of 1.11 to 1.14 and the activity ratios of sup (235) U/ sup(235) U are in the range of 0.045 to 0.047. The respective...

  6. Transfer Rates of ²³⁸U and ²³²Th for E. globulus, A. mearnsii, H. filipendula and Hazardous Effects of the Usage of Medicinal Plants From Around Gold Mine Dump Environs.

    Science.gov (United States)

    Tshivhase, Victor M; Njinga, Raymond L; Mathuthu, Manny; Dlamini, Thulani C

    2015-12-10

    Medicinal plant consumption can be a source of human exposure to radioactive elements such as (238)U and (232)Th, which can lead to internal radiation doses. The uptake of (238)U and (232)Th from soils to the leaf samples of three different medicinal plant species (Eucalyptus globulus, Acacia mearnsii and Hyparrhenia filipendula) from the purlieu of the Princess gold mine dump, an abandoned contaminated tailings storage site (TSS), located at longitude 27°55'00″E and latitude 26°09'30″S in Davidsonville (Roodepoort, west of Johannesburg, South Africa) was measured. This was done using ICP-MS spectrometry and substantial differences were observed in the soil-plant transfer factor (TF) values between these radionuclides. The plant species E. globulus exhibited the highest uptake of (238)U, with an average TF of 3.97, while that of H. filipendula was 0.01 and the lowest TF of 0.15 × 10(-2) was measured for A. mearnsii. However, in the case of (232)Th, the highest average TF was observed for A. mearnsii (0.29), followed by E. globulus (0.10) and lowest was measured for H. filipendula (0.27 × 10(-2)). The ratio of TF average value i.e., (238)U to (232)Th in the soil-plant leaves was 38.05 for E. globulus, 0.01 for A. mearnsii and 4.38 for H. filipendula.

  7. Geochemistry of uranium and thorium and natural radioactivity levels of the western Anatolian plutons, Turkey

    Science.gov (United States)

    Papadopoulos, Argyrios; Altunkaynak, Şafak; Koroneos, Antonios; Ünal, Alp; Kamaci, Ömer

    2017-01-01

    Seventy samples from major plutons (mainly granitic) of Western Anatolia (Turkey) have been analyzed by γ-ray spectrometry to determine the specific activities of 238U, 226Ra, 232Th and 40K (Bq/kg). Τhe natural radioactivity ranged up to 264 Bq/kg for 238U, 229.62 Bq/kg for 226Ra, up to 207.32 Bq/kg for 232Th and up to 2541.95 Bq/kg for 40K. Any possible relationship between the specific activities of 226Ra, 238U, 232Th and 40K and some characteristics of the studied samples (age, rock-type, colour, grain size, occurrence, chemical and mineralogical composition) was investigated. Age, major and trace element geochemistry, color, pluton location and mineralogical composition are likely to affect the concentrations of the measured radionuclides. The range of the Th/U ratio was large (0.003-11.374). The latter, along with 226Ra/238U radioactive secular disequilibrium, is also discussed and explained by magmatic processes during differentiation.

  8. ASSESSMENT OF AGE-DEPENDENT RADIATION DOSE DUE TO INTAKE OF URANIUM AND THORIUM IN DRINKING WATER FROM SIKAR DISTRICT, RAJASTHAN, INDIA.

    Science.gov (United States)

    Duggal, Vikas; Rani, Asha; Balaram, V

    2016-10-01

    The concentrations of (238)U and (232)Th have been determined in drinking water samples collected from the Sikar district of Rajasthan State, India. The samples have been analysed by using high-resolution inductively coupled plasma mass spectrometry. (238)U content in water samples ranged from 8.20 to 202.63 µg l(-1) and (232)Th content ranged from 0.57 to 1.46 µg l(-1) The measured (238)U content in 25 % of the analysed samples exceeded the World Health Organization (WHO) and United States Environmental Protection Agency drinking water guidelines of 30 µg l(-1) and 12.5 % of the samples exceeded the 60 µg l(-1) Indian maximum acceptable concentration recommended by the Atomic Energy Regulatory Board, India. The annual effective doses (µSv y(-1)) due to ingestion of (238)U and (232)Th for different age groups were also calculated. The results compared with the recommended value reported by the WHO. © The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  9. The radiological impact of phosphogypsum stockpile in Wiślinka (northern Poland) on the Martwa Wisła river water.

    Science.gov (United States)

    Olszewski, Grzegorz; Boryło, Alicja; Skwarzec, Bogdan

    The aim of this work was to determine the concentrations of uranium ((234)U, (235)U, (238)U), polonium ((210)Po) and lead ((210)Pb) radioisotopes in water samples and to explore the impact of the phosphogypsum stack on the Martwa Wisła waters. The (238)U, (210)Po and (210)Pb concentrations in analyzed water samples reached maximum values of 11.7 ± 0.3, 2.0 ± 0.1 and 3.2 ± 0.1 mBq L(-1) and activity ratios were maximally 1.18 ± 0.01 for (234)U/(238)U, 0.041 ± 0.018 for (235)U/(238)U and 0.69 ± 0.10 for (210)Po/(210)Pb. The obtained results suggest that this impact is rather insignificant and does not affect significantly the Martwa Wisła river.

  10. Anomalous behaviour of uranium isotopes in backwater sediments of Zuari river

    Digital Repository Service at National Institute of Oceanography (India)

    Joshi, L.U; Zingde, M.D.; Abidi, S

    The surface leaching of the labile component of uranium has been carried out in estuarine sediments of Zuari River in Goa, India The measurements of alpha activities of sup(238) U, sup(235) U and sup(234) U in the leachates indicated a remarkable...

  11. The absorption and scavenging ability of a bacillus on the of heavy ...

    African Journals Online (AJOL)

    微软用户

    2014-09-05

    Sep 5, 2014 ... radioactive materials (NORMs) from 238U and 232Th and their respective ... radionuclides in the end products and wastes of the phosphate industry. .... MATERIALS AND METHODS ... (Jamok, 2014), and stored at room temperature for a period of 5 .... phosphate rock samples is above the proposed safety.

  12. Determination of uranium from nuclear fuel in environmental samples using inductively coupled plasma mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Boulyga, S.F. [Forschungszentrum Juelich GmbH (Germany). Zentralabteilung fuer Chemische Analysen]|[Radiation Physics and Chemistry Problems Inst., Minsk (Belarus); Becker, J.S. [Forschungszentrum Juelich GmbH (Germany). Zentralabteilung fuer Chemische Analysen

    2000-11-01

    As a result of the accident at the Chernobyl nuclear power plant (NPP) the environment was contaminated with spent nuclear fuel. The {sup 236}U isotope was used in this study to monitor the spent uranium from nuclear fallout in soil samples collected in the vicinity of the Chernobyl NPP. A rapid and sensitive analytical procedure was developed for uranium isotopic ratio measurement in environmental samples based on inductively coupled plasma quadrupole mass spectrometry with a hexapole collision cell (HEX-ICP-QMS). The figures of merit of the HEX-ICP-QMS were studied with a plasma-shielded torch using different nebulizers (such as an ultrasonic nebulizer (USN) and Meinhard nebulizer) for solution introduction. A {sup 238}U{sup +} ion intensity of up to 27000 MHz/ppm in HEX-ICP-QMS with USN was observed by introducing helium into the hexapole collision cell as the collision gas at a flow rate of 10 ml min{sup -1}. The formation rate of uranium hydride ions UH{sup +}/U{sup +} of 2 x 10{sup -6} was obtained by using USN with a membrane desolvator. The limit of {sup 236}U/{sup 238}U ratio determination in 10 {mu}g 1{sup -1} uranium solution was 3 x 10{sup -7} corresponding to the detection limit for {sup 236}U of 3 pg 1{sup -1}. The precision of uranium isotopic ratio measurements in 10 {mu}g 1{sup -1} laboratory uranium isotopic standard solution was 0.13% ({sup 235}U/{sup 238}U) and 0.33% ({sup 236}U/{sup 238}U) using a Meinhard nebulizer and 0.45% ({sup 235}U/{sup 238}U) and 0.88% ({sup 236}U/{sup 238}U) using a USN. The isotopic composition of all investigated Chernobyl soil samples differed from those of natural uranium; i.e. in these samples the {sup 236}U/{sup 238}U ratio ranged from 10{sup -5} to 10{sup -3}. (orig.)

  13. Determining the isotopic compositions of uranium and fission products in radioactive environmental microsamples using laser ablation ICP-MS with multiple ion counters.

    Science.gov (United States)

    Boulyga, Sergei F; Prohaska, Thomas

    2008-01-01

    This paper presents the application of a multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS)--a Nu Plasma HR--equipped with three ion-counting multipliers and coupled to a laser ablation system (LA) for the rapid and sensitive determination of the 235U/238U, 236U/238U, 145Nd/143Nd, 146Nd/143Nd, 101Ru/(99Ru+99Tc) and 102Ru/(99Ru+99Tc) isotope ratios in microsamples collected in the vicinity of Chernobyl. Microsamples with dimensions ranging from a hundred mum to about 1 mm and with surface alpha activities of 3-38 mBq were first identified using nuclear track radiography. U, Nd and Ru isotope systems were then measured sequentially for the same microsample by LA-MC-ICP-MS. The application of a zoom ion optic for aligning the ion beams into the ion counters allows fast switching between different isotope systems, which enables all of the abovementioned isotope ratios to be measured for the same microsample within a total analysis time of 15-20 min (excluding MC-ICP-MS optimization and calibration). The 101Ru/(99Ru+99Tc) and 102Ru/(99Ru+99Tc) isotope ratios were measured for four microsamples and were found to be significantly lower than the natural ratios, indicating that the microsamples were contaminated with the corresponding fission products (Ru and Tc). A slight depletion in 146Nd of about 3-5% was observed in the contaminated samples, but the Nd isotopic ratios measured in the contaminated samples coincided with natural isotopic composition within the measurement uncertainty, as most of the Nd in the analyzed samples originates from the natural soil load of this element. The 235U/238U and 236U/238U isotope ratios were the most sensitive indicators of irradiated uranium. The present work yielded a significant variation in uranium isotope ratios in microsamples, in contrast with previously published results from the bulk analysis of contaminated samples originating from the vicinity of Chernobyl. Thus, the 235U/238U ratios measured in ten

  14. Radioactivity in three species of eastern Mediterranean jellyfish.

    Science.gov (United States)

    Mamish, S; Al-Masri, M S; Durgham, H

    2015-11-01

    Activity concentrations of (137)Cs, (40)K, (210)Po, (210)Pb, (234)U and (238)U were determined in umbrella and oral arms of three widely distributed jellyfish species; namely Rhopilema nomadica Galil, 1990, Aurelia aurita Linne, 1758 and Aequorea forskalea Péron & Lesueur, 1810 collected from February 2011 to January 2012 in four sampling locations along the Syrian coast (Eastern Mediterranean Sea). The results have shown significant variations in radionuclides activity concentrations amongst the species. The average activity concentrations of (40)K, (210)Po, (210)Pb, (234)U and (238)U in the umbrella of R. nomadica species were higher than the average activity concentrations in the umbrella of A. aurita species by about 3.2, 1.4, 1.8, 3.2 and 3.2 folds, and A. forskalea species by about 45.5, 15.4, 19, 7.4 and 7.6 folds, respectively. The average activity concentrations of (40)K, (210)Po, (210)Pb, (234)U and (238)U in oral arms of R. nomadica species were higher than the average activity concentrations in oral arms of A. aurita species by about 3.8, 1.7, 1.9, 2.8 and 2.9 folds, respectively. (137)Cs activity concentrations were below the detection limit in all measured samples. In addition, activity concentrations of (137)Cs, (40)K, (210)Po, (210)Pb, (234)U and (238)U were also determined in 44 surface seawater samples and the activity concentrations ranged between 10.6 and 11.9 Bq l(-1) for (40)K, 1.1 and 1.4 mBq l(-1) for (210)Po, 0.5 and 0.7 mBq l(-1) for (210)Pb, 40.8 and 44.5 mBq l(-1) for (234)U, and 36.9 and 38.4 mBq l(-1) for (238)U, while (137)Cs activity concentrations were below the detection limit in all measured samples. Moreover, the umbrella and oral arms readily accumulated (40)K, (210)Po, (210)Pb, (234)U and (238)U above ambient seawater levels in the sequence of (210)Po > (210)Pb > (4) K > (234)U and (238)U. Concentration ratio (CR) values were relatively high for (210)Po and (210)Pb and reached 10(3) and 10(2), respectively for the jellyfish R

  15. Geoquímica de radionuclídeos naturais em solos de áreas circunvizinhas a uma Unidade de Mineração e Atividade de Urânio Geochemistry of natural radionuclide in soils surrounding a Mining and Plant Uranium Concentration

    Directory of Open Access Journals (Sweden)

    Gildevan Viana Cardoso

    2009-12-01

    Full Text Available Os impactos ambientais advindos da exploração e do beneficiamento de U são, em grande parte, idênticos àqueles causados por atividades minero-extrativistas em geral. Este trabalho teve o objetivo de determinar a partição geoquímica dos radionuclídeos naturais 238U, 226Ra e 210Pb em áreas circunvizinhas à Unidade de Mineração e Atividade de Urânio (URA das Indústrias Nucleares do Brasil S.A., localizada na Província Uranífera de Lagoa Real, no município de Caetité, na região sudoeste do Estado da Bahia. Foram coletadas amostras de solo em cinco áreas circunvizinhas à URA, representando as principais classes de solos da região, na profundidade de 0-20 cm. Nas cinco áreas, foram determinados o teor de atividade total e o fracionamento geoquímico nas frações: F1 - levemente ácida, F2 - reduzível, F3 - oxidável, F4 - alcalina e F5 - residual. As atividades totais médias foram, em Bq kg-1 de solo, de 50 para 238U, 51 para 226Ra e 159 para 210Pb. Os extraídos na fase potencialmente biodisponível (F1 foram: 11 % para 238U, 13 % para 226Ra e 3 % para 210Pb. O 238U apresentou maior biodisponibilidade nos solos mais ácidos e maior afinidade pelos óxidos de Fe, o que não ocorreu para o 226Ra, tendo este apresentado a maior biodisponibilidade. O 210Pb apresentouse predominantemente associado a F5. As percentagens elevadas de 238U, 226Ra e 210Pb na fração geoquímica F5 indicam que as atividades observadas nos cinco solos estão, predominantemente, associadas ao material que deu origem a esses solos, e não a um processo de contaminação artificial em função da atividade da URA.The environmental impacts resulting from uranium exploration and processing are to a great extent identical to those caused by extractive mining activities in general. This study aimed to determine the geochemical partitioning of the natural radionuclides 238U, 226Ra and 210Pb in areas surrounding the Uranium Mining and Concentration Plant (URA

  16. Geochemistry of natural radionuclide in soils surrounding a mining and plant uranium concentration;Geoquimica de radionuclindeos naturais em solos de areas circunvizinhas a uma unidade de mineracao e atividade de uranio

    Energy Technology Data Exchange (ETDEWEB)

    Cardoso, Gildevan Viana, E-mail: gildevan.cardoso@vta.incra.gov.b [Instituto Nacional de Colonizacao e Reforma Agraria (INCRA), Rio de Janeiro, RJ (Brazil); Amaral Sobrinho, Nelson Moura Brasil do; Mazur, Nelson, E-mail: nelmoura@ufrrj.b, E-mail: nelmazur@ufrrj.b [Universidade Federal Rural do Rio de Janeiro (UFRRJ), Seropedica, RJ (Brazil). Inst. de Agronomia. Dept. de Solos; Wasserman, Maria Angelica Vergara, E-mail: angelica@ird.gov.b [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

    2009-11-15

    The environmental impacts resulting from uranium exploration and processing are to a great extent identical to those caused by extractive mining activities in general. This study aimed to determine the geochemical partitioning of the natural radionuclides {sup 238}U, {sup 226}Ra and {sup 210}Pb in areas surrounding the Uranium Mining and Concentration Plant (URA) of the Brazilian Nuclear Industries S.A., in the uranium deposit region of Lagoa Real, in Caetite, southwestern Bahia state. Representative soil samples of the main regional soil classes were collected from the layer 0-20 cm, in five areas around the URA. The level of total activity and geochemical fractionation (F1 slightly acidic, F2 reducible, F3 oxidisable, F4 alkaline, and F5 residual) were determined for the five areas. The average total radioactivity levels were, in Bq kg{sup -1} soil: 50 for {sup 238}U, 51 for {sup 226}Ra, and 159 for {sup 210}Pb. During the potentially bioavailable phase (F1) 11 % were extracted for {sup 238}U, 13 % for {sup 226}Ra and 3 % for {sup 210}Pb. The bioavailability of {sup 238}U was higher in more acidic soils and the affinity for iron oxides was greater, unlike in the case of {sup 226}Ra, with the greatest bioavailability. {sup 210}Pb was predominantly associated with F5. The high percentage of {sup 238}U, {sup 226}Ra and {sup 210}Pb in the geochemical fraction F5 indicates that the concentrations observed in the five soils are predominantly associated to the parent material of these soils, rather than to an artificial contamination caused by the URA activity. (author)

  17. Development of methodologies used in the areas of safeguards and nuclear forensics based on LA-HR-ICP-MS technique; Desenvolvimento de metodologias utilizadas nas areas de salvaguardas e forense nuclear baseadas na tecnica LA-HR-ICP-MS

    Energy Technology Data Exchange (ETDEWEB)

    Marin, Rafael Coelho

    2013-07-01

    Environmental sampling performed by means of swipe samples is a methodology frequently employed by International Atomic Energy Agency (IAEA) to verify if the signatory States of the Safeguards Agreements are conducing unauthorized activities. Swipe samples analysis is complementary to the Safeguards ordinary procedures used to verify the information given by the States. In this work it was described a methodology intending to strengthen the nuclear safeguards and nuclear forensics procedures. The proposal is to study and evaluate the laser ablation high resolution inductively coupled plasma mass spectrometry (LA-HR-ICP-MS) technique as an alternative to analyze the real-life swipe samples. The precision achieved through the standard (CRM - 125A) measurements, represented by the relative standard deviation (RSD), was respectively 1.3 %, 0.2 % e 7.6 % for the {sup 234}U/{sup 238}U, {sup 235}U/{sup 238}U e {sup 236}U/{sup 238}U isotopes ratios. The percent uncertainties (u %), which covers the RSD, ranged from 3.5 % to 29.8 % to the {sup 235}U/{sup 238}U measurements and from 16.6 % to 42.9 % to the {sup 234}U/{sup 238}U isotope ratio. These results were compatible with former studies performed by the LA-HR-ICP-MS that analyzed real-life swipe samples collected at a nuclear facility. Swipe samples collected from several points of the nuclear facility presented enrichment level ranging from (2.3 ± 0.7) % (sample 3) to (17.3 ± 2.8) % (sample 18). They also allowed detecting different enrichment levels within the facility. (author)

  18. A study on the impact of phosphate fertilizers on the radioactivity profile of cultivated soils in Srirangam (Tamil Nadu, India

    Directory of Open Access Journals (Sweden)

    P. Shahul Hameed

    2014-10-01

    Full Text Available Phosphate fertilizers are enriched with 238U during its production from phosphate rocks. Since, application of phosphate fertilizers in modern agriculture is ever on the increase, the present study investigated the impact of phosphate fertilizers on the radioactivity profile of cultivated (fertilized soils as against virgin soils. Thirty soil samples each from cultivated fields and virgin fields were collected from Srirangam taluk and analyzed for the activity concentrations of 238U, 232Th and 40K employing gamma ray spectrometry. Similar analysis was also undertaken in commonly used phosphate fertilizers. Among the phosphate fertilizers analyzed single super phosphate (396.3 Bq/kg and triple super phosphate (284.2 Bq/kg registered higher level of 238U. The mean activity level of 238U in cultivated soil (8.4 Bq/kg was 25% higher than that of virgin soil (6.8 Bq/kg, while the mean 232Th and 40K activities in cultivated soil (98.4 Bq/kg & 436 Bq/kg were elevated by 12.4% and 4% respectively as compared to virgin soil (87.5 Bq/kg & 419 Bq/kg. The mean radium equivalent (Raeq value for virgin and cultivated soil samples was found to be 164.5 Bq/kg and 181.7 Bq/kg respectively. It is evident that the application of phosphate fertilizers elevated 238U level of the soil. However, the mean Raeq value for soil samples is well below the permissible limit of 370 Bq/kg and hence cultivated soils do not pose any radiological risk.

  19. Dependency of renal thorium and uranium excretion from age and gender in non-exposed persons; Abhaengigkeit der renalen Thorium- und Uranausscheidung von Geschlecht und Alter bei nicht-exponierten Personen

    Energy Technology Data Exchange (ETDEWEB)

    Werner, E.; Roth, P.; Wendler, I.; Schramel, P. [GSF - Forschungszentrum fuer Umwelt und Gesundheit GmbH, Neuherberg (Germany)

    1998-12-31

    For the assessment of an occupational incorporation of thorium or uranium it is essential to know which portion of the measured activity is caused by natural sources. In the present study the daily urinary excretion of {sup 232}Th and {sup 238}U was measured in 76 healthy volunteers. None of them had a previous history of occupational exposure to thorium or uranium. The data show no difference in the excretion between male and female subjects. Whereas in adolescents only little excretion of {sup 232}Th and {sup 238}U is found, a significantly increasing variation of thorium and uranium in urine is observed with progressing age. From the data obtained an age-related upper limit of {sup 232}Th and {sup 238}U urinary excretion can be derived, which may be useful for the interpretation of a measured value due to the occupational exposure. (orig.) [Deutsch] Fuer die Beurteilung einer beruflich bedingten Inkorporation von Thorium oder Uran ist es wichtig zu wissen, welcher Artikel am gemessenen Wert auf natuerliche Quellen zurueckzufuehren ist. In der vorliegenden Studie wurde die taegliche Ausscheidung von{sup 232}Th und {sup 238}U im Urin bei 76 gesunden Personen im Alter von 7 bis 84 Jahren mit der ICP-MS gemessen. Keine dieser Personen hatte vorher beruflichen Umgang mit Thorium oder Uran gehabt. Die Daten zeigen keinen Unterschied zwischen Frauen und Maennern. Waehrend bei Jugendlichen nur geringe Ausscheidungswerte beobachtet werden, tritt mit zunehmendem Lebensalter eine erhebliche Vergroesserung des Variationsbereichs ein. Aus den erhobenen Daten ergibt sich eine altersbezogene Obergrenze fuer die {sup 232}Th- und {sup 238}U-Ausscheidung im Urin, die fuer die Interpretation eines Messwertes bei beruflicher Exposition herangezogen werden kann. (orig.)

  20. 贫铀/聚乙烯交替球壳中裂变反应率的测量与分析%Measurement and Analysis of Fission Rate in Alternate Depleted Uranium/Polyethylene Shells

    Institute of Scientific and Technical Information of China (English)

    严小松; 羊奕伟; 朱通华; 刘荣; 鹿心鑫; 蒋励

    2013-01-01

    In order to check the conceptual design of the subcritical blanket in fusion-fission hybrid reactor, an integral experiment was carried out in alternate depleted uranium/polyethylene shells with 14 MeV neutron using activation technique. The 238U(n,f) and 235U(n,f) reaction rates at 90?direction to the incident D beam were determined by measuring the 293. 3 keV y ray emitted from I43Ce which is generated by 238U(n,f) and 235U(n,f) reactions. The experiment was simulated using MCNP5 code with ENDF/B-Ⅵ library, and the calculated 238U(n,f) and 235U(n,f) reaction rates are generally 5% higher than experimental results.%为校验次临界能源堆的概念设计,采用活化法在贫铀/聚乙烯球壳交替装置上开展14 MeV中子学积分实验.用HPGe探测器测量238U(n,f)及235U(n,f)反应的裂变碎片143Ce衰变产生的293.3 keV特征γ射线,得到装置中与入射D粒子束成90°方向上的238U(n,f)及235U(n,f)反应率分布,相对不确定度为5.1%~6.9%.采用MCNP5程序在ENDF/B-Ⅵ库下进行模拟计算,计算结果较实验结果高约5%.

  1. Determination of uranium isotopic composition and 236U content of soil samples and hot particles using inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Boulyga, S F; Becker, J S

    2001-07-01

    As a result of the accident at the Chernobyl nuclear power plant (NPP) the environment was contaminated with spent nuclear fuel. The 236U isotope was used in this study to monitor the spent uranium from nuclear fallout in soil samples collected in the vicinity of the Chernobyl NPP. Nuclear track radiography was applied for the identification and extraction of hot radioactive particles from soil samples. A rapid and sensitive analytical procedure was developed for uranium isotopic ratio measurement in environmental samples based on double-focusing inductively coupled plasma mass spectrometry (DF-ICP-MS) with a MicroMist nebulizer and a direct injection high-efficiency nebulizer (DIHEN). The performance of the DF-ICP-MS with a quartz DIHEN and plasma shielded torch was studied. Overall detection efficiencies of 4 x 10(-4) and 10(-3) counts per atom were achieved for 238U in DF-ICP-QMS with the MicroMist nebulizer and DIHEN, respectively. The rate of formation of uranium hydride ions UH+/U+ was 1.2 x 10(-4) and 1.4 x 10(-4), respectively. The precision of short-term measurements of uranium isotopic ratios (n = 5) in 1 microg L(-1) NBS U-020 standard solution was 0.11% (238U/235U) and 1.4% (236U/238U) using a MicroMist nebulizer and 0.25% (235U/238U) and 1.9% (236U/P38U) using a DIHEN. The isotopic composition of all investigated Chernobyl soil samples differed from those of natural uranium; i.e. in these samples the 236U/238U ratio ranged from 10(-5) to 10(-3). Results obtained with ICP-MS, alpha- and gamma-spectrometry showed differences in the migration properties of spent uranium, plutonium, and americium. The isotopic ratio of uranium was also measured in hot particles extracted from soil samples.

  2. Determination of (236)U in environmental samples by single extraction chromatography coupled to triple-quadrupole inductively coupled plasma-mass spectrometry.

    Science.gov (United States)

    Yang, Guosheng; Tazoe, Hirofumi; Yamada, Masatoshi

    2016-11-09

    In order to measure trace (236)U and (236)U/(238)U in environmental samples with a high matrix effect, a novel and simple method was developed that makes the digestion and purification procedures compatible with advanced triple-quadrupole inductively coupled plasma-mass spectrometry. A total dissolution of sample with HF + HNO3 + HClO4 was followed by chromatographic separation with a single resin column containing normal type DGA resin (N,N,N',N'-tetra-n-octyldiglycolamide) as the extractant system. The analytical accuracy and precision of (236)U/(238)U ratios, measured as (236)U(16)O(+)/(238)U(16)O(+), were examined by using the reference materials IAEA-135, IAEA-385, IAEA-447, and JSAC 0471. The low method detection limit (3.50 × 10(-6) Bq kg(-1)) makes it possible to perform routine monitoring of environmental (236)U due to global fallout combined with the Fukushima Daiichi Nuclear Power Plant accident fallout (>10(-5) Bq kg(-1)). Finally, the developed method was successfully applied to measure (236)U/(238)U ratios and (236)U activities in soil samples contaminated by the accident. The low (236)U/(238)U atom ratios ((1.50-13.5) × 10(-8)) and (236)U activities ((2.25-14.1) × 10(-2) mBq kg(-1)) indicate (236)U contamination was mainly derived from global fallout in the examined samples.

  3. Natural radioactivity of some spring and bottled mineral waters from several central Balkan sites, as a way of their characterization

    Directory of Open Access Journals (Sweden)

    SCEPAN S. MILJANIC

    2007-06-01

    Full Text Available In this work, a study of the radioactive content of some spring and bottled mineral waters originating frommetamorphic rock areas was carried out.Ahigh content of radium isotopes (226Ra, 228Ra, was found by radiometric analysis in the spring waters: Studenica (226Ra: 289 mBq/L, ^ibutkovica (226Ra: 92, 4 mBq/L, 228Ra: 610 mBq/L, and Crni Guber (226Ra: 120 mBq/L, 228Ra: 1170 mBq/L. On the other hand, the radiochemical results showed a higher concentration of 238U in the bottled mineral water samples (dissolved uranium concentrations were from 0.21 mBq/L, for "Kopaonik" to 71.5mBq/L fo "Skadarska" than in the spring water samples (dissolved uranium concentrations were very low » 10 mBq/L. The concentrations of all the present naturally occuring radionuclides: 238U, 234U, 232Th, 230Th, 228Th, 228Ra and 226Ra were determined by alpha/gamma spectrometric analysis. The activity ratios 234U/238U, 226Ra/230Th and 228Th/232Th, 228Ra/228Th were calculated and are discussed as an indication of the radioactive disequilibrium in bothe the 238U and 232Th radioactive series. The high contents of radium isotopes with respect to the equilibrium values expected from the respective parents 232Th/(232Th series and 230Th (238U series found in the spring water samples is the main evidence for the existence of significant radioactive disequilibrium in both the radioactive series.

  4. Synchronizing terrestrial and marine records of environmental change across the Eocene-Oligocene transition

    Science.gov (United States)

    Sahy, Diana; Condon, Daniel J.; Terry, Dennis O.; Fischer, Anne U.; Kuiper, Klaudia F.

    2015-10-01

    Records of terrestrial environmental change indicate that continental cooling and/or aridification may have predated the greenhouse-icehouse climate shift at the Eocene-Oligocene transition (EOT) by ca. 600 kyr. In North America, marine-terrestrial environmental change asynchronicity is inferred from a direct comparison between the astronomically tuned marine EOT record and published 40Ar/39Ar geochronology of volcanic tuffs from the White River Group (WRG) sampled at Flagstaff Rim (Wyoming) and Toadstool Geologic Park (Nebraska), which are type sections for the Chadronian and Orellan North American Land Mammal Ages. We present a new age-model for the WRG, underpinned by high-precision 206Pb/238U zircon dates from 15 volcanic tuffs, including six tuffs previously dated using the 40Ar/39Ar technique. Weighted mean zircon 206Pb/238U dates from this study are up to 1.0 Myr younger than published anorthoclase and biotite 40Ar/39Ar data (calibrated relative to Fish Canyon sanidine at 28.201 Ma). Giving consideration to the complexities, strengths, and limitations associated with both the 40Ar/39Ar and 206Pb/238U datasets, our interpretation is that the recalculated 40Ar/39Ar dates are anomalously old, and the 206Pb/238U (zircon) dates more accurately constrain deposition. 206Pb/238U calibrated age-depth models were developed in order to facilitate a robust intercomparison between marine and terrestrial archives of environmental change, and indicate that: (i) early Orellan (terrestrial) cooling recorded at Toadstool Geologic Park was synchronous with the onset of early Oligocene Antarctic glaciation and (ii) the last appearance datums of key Chadronian mammal taxa are diachronous by ca. 0.7 Myr between central Wyoming and NW Nebraska.

  5. Rapid screening of natually occurring radioactive nuclides({sup 2}'3{sup 8}U, {sup 232}Th) in raw materials and by-products samples using XRF

    Energy Technology Data Exchange (ETDEWEB)

    Park, Ji Young; Lim, Chung Sup [Radiation Biotechnology and Applied Radioiostope Science, University of Science and Technology, Daejeon (Korea, Republic of); Lim, Jong Myoung; Ji, Young Yong; Chung, Kun Ho; Lee, Wan No; Kang, Mun Ja [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of); Jang, Byung Uck [Korea Institute of Nuclear Safety, Daejeon (Korea, Republic of)

    2016-12-15

    As new legislation has come into force implementing radiation safety management for the use of naturally occurring radioactive materials (NORM), it is necessary to establish a rapid and accurate measurement technique. Measurement of {sup 238}U and {sup 232}Th using conventional methods encounter the most significant difficulties for pretreatment (e.g., purification, speciation, and dilution/enrichment) or require time-consuming processes. Therefore, in this study, the applicability of ED-XRF as a non-destructive and rapid screening method was validated for raw materials and by-product samples. A series of experiments was conducted to test the applicability for rapid screening of XRF measurement to determine activity of {sup 238}U and {sup 23{sup 2}}Th based on certified reference materials (e.g., soil, rock, phosphorus rock, bauxite, zircon, and coal ash) and NORM samples commercially used in Korea. Statistical methods were used to compare the analytical results of ED-XRF to those of certified values of certified reference materials (CRM) and inductively coupled plasma mass spectrometry (ICP-MS). Results of the XRF measurement for {sup 238}U and {sup 232}Th showed under 20% relative error and standard deviation. The results of the U-test were statistically significant except for the case of U in coal fly ash samples. In addition, analytical results of {sup 238}U and {sup 232}Th in the raw material and by-product samples using XRF and the analytical results of those using ICP-MS (R{sup 2}≥0.95) were consistent with each other. Thus, the analytical results rapidly derived using ED-XRF were fairly reliable. Based on the validation results, it can be concluded that the ED-XRF analysis may be applied to rapid screening of radioactivities ({sup 238}U and {sup 232}Th) in NORM samples.

  6. Polonium, uranium and plutonium radionuclides in aquatic and land ecosystem of Poland.

    Science.gov (United States)

    Skwarzec, Bogdan; Strumińska-Parulska, Dagmara I; Boryło, Alicja; Kabat, Krzysztof

    2012-01-01

    This article presents the results of study about distribution, inflow and accumulation of polonium, uranium and plutonium in aquatic and land environment of Poland and the southern Baltic Sea. Radionuclides of (210)Po, (234)U and (238)U as well as (239+240)Pu and (241)Pu are strongly accumulated in Baltic organisms and plants and transferred through the trophic chain. The values of bioconcentration factor (BCF) in Baltic plants and animals are higher for polonium and plutonium in comparison with uranium. The principal source of radionuclides in the southern Baltic Sea is their inflow with rivers. Total annual runoff of polonium, uranium and plutonium from the Vistula and the Odra as well as the Pomeranian rivers were calculated at 95 GBq of (210)Po, 750 GBq of (234+238)U and 160 MBq of (238+239+240)Pu. Seasonal and spatial variability of (210)Po, (238)U and (239+240)Pu levels in the Vistula and the Odra drainage basins were assessed by application of neural-network based classification, especially cluster analysis (CA), principal component analysis (PCA) and self-organizing maps (SOM). The result for the Vistula river indicated correlation between polonium and plutonium as well as polonium and uranium. In the Odra drainage basin, the biggest differences were observed in the case of (238)U. To assess if there are statistically significant differences in mean concentration values of (210)Po, (238)U and (239+240)Pu for the Vistula and the Odra rivers drainage basins were obtained by used of the non-parametric tests. Comparing to the Vistula catchment area, statistically differences concentration of (210)Po and (239+240)Pu in all year was observed for river samples collected on the Odra drainage basin.

  7. The radiochemical contamination (²¹⁰Po and ²³⁸U) of zone around phosphogypsum waste heap in Wiślinka (northern Poland).

    Science.gov (United States)

    Boryło, Alicja; Skwarzec, Bogdan; Olszewski, Grzegorz

    2012-01-01

    The aim of this work was the determination of the impact of phosphogypsum waste heap in Wiślinka (northern Poland) for radiological protection of zone around waste heap. These studies are very important for the estimation of natural alpha radionuclides contents in the vicinity of phosphogypsum waste heap and for environmental pollution assessment of this area. The process of bioaccumulation of radionuclides in interior plants parts prove to examine their origin sources, too. The activity of (210)Po, (234)U, and (238)U were measured using an alpha spectrometer. The values of uranium and polonium concentration in water with immediate area of waste heap are considerably higher than in the waters of the Martwa Wisła river. The values of activity ratio (234)U/(238)U are approximately about one in the phosphogypsum (0.97 ± 0.05) and in the water of retention reservoir and pumping station (0.92 ± 0.01 and 0.99 ± 0.08), while in the water from the Martwa Wisła river they are slightly higher than one (1.03 ± 0.07 and 1.17 ± 0.06). In the analyzed plants species the highest amounts of polonium and uranium were found in ruderal plants samples (between 51 ± 1 and 89 ± 1 for (210)Po; between 36 ± 3 and 68 ± 3 for (238)U) as well as hygrophilous plant samples (18 ± 1 and 84 ± 3; 42 ± 2 and 130 ± 4, respectively for (210)Po and (238)U). The more amounts of (210)Po and (238)U radionuclides were accumulated mainly in the roots of plant species in comparison to green parts. The general conclusion of realized study is higher influence of phosphogypsum on radioactive contamination of environmental zone around heap waste in Wiślinka (northern Poland).

  8. Precise and accurate measurement of U and Th isotopes via ICP-MS using a single solution

    Science.gov (United States)

    Mertz-Kraus, R.; Sharp, W. D.; Ludwig, K. R.

    2012-04-01

    U-series isotope measurements by ICP-MS commonly utilize separate runs for U and Th and standard-sample bracketing to determine correction factors for mass fractionation and ion counter yields. Here we present an approach where all information necessary to calculate an age (aside from background/baseline levels) is determined while analyzing a single solution containing both U and Th. This internally calibrated procedure should reduce any bias caused by distinct behavior of sample versus standard solutions during analysis and offers advantages including simplicity of operation, calculation of preliminary ages in real time, and simplified analysis of errors and their sources. Hellstrom (2003) developed a single-solution, internally-calibrated technique for an ICP-MS with multiple ion counters, but to our knowledge no such technique is available for an ICP-MS with a single ion counter. We use a Thermo Neptune Plus multi-collector ICP-MS with eight movable Faraday cups and a fixed center cup/ion counter equipped with a high abundance-sensitivity filter (RPQ). We use Faraday cups to measure all masses except 230 and 234, which are measured on the ion counter with the RPQ detuned (i.e., Suppressor voltage = 9950 V). 238U is maintained in a cup throughout the analysis to avoid reflections and is used to normalize signal instabilities related to sample introduction. Each analysis has a three-part structure, i.e. 1) background/baseline levels, 2) sample composition, and 3) peak-tails are sequentially determined. In step 1, multiplier dark noise/Faraday baselines plus background intensities at each mass are determined while aspirating running solution. During sample measurement in step 2, ion counter yields for Th and U are determined using signals of 300-400 kcps for 229Th and 233U by measuring 229Th/238U and 233U/238U ratios first with the minor masses on the ion counter and then with both masses in cups. Mass bias can be determined using the 233U/236U ratio of the spike

  9. U-Sr isotopic speedometer: Fluid flow and chemical weatheringrates inaquifers

    Energy Technology Data Exchange (ETDEWEB)

    Maher, Kate; DePaolo, Donald J.; Christensen, John N.

    2005-12-27

    Both chemical weathering rates and fluid flow are difficultto measure in natural systems. However, these parameters are critical forunderstanding the hydrochemical evolution of aquifers, predicting thefate and transport of contaminants, and for water resources/water qualityconsiderations. 87Sr/86Sr and (234U/238U) activity ratios are sensitiveindicators of water-rock interaction, and thus provide a means ofquantifying both flow and reactivity. The 87Sr/86Sr values in groundwaters are controlled by the ratio of the dissolution rate to the flowrate. Similarly, the (234U/238U) ratio of natural ground waters is abalance between the flow rate and the dissolution of solids, andalpha-recoil loss of 234U from the solids. By coupling these two isotopesystems it is possible to constrain both the long-term (ca. 100's to1000's of years) flow rate and bulk dissolution rate along the flow path.Previous estimates of the ratio of the dissolution rate to theinfiltration flux from Sr isotopes (87Sr/86Sr) are combined with a modelfor (234U/238U) to constrain the infiltration flux and dissolution ratefor a 70-m deep vadose zone core from Hanford, Washington. The coupledmodel for both (234U/238U) ratios and the 87Sr/86Sr data suggests aninfiltration flux of 5+-2 mm/yr, and bulk silicate dissolution ratesbetween 10-15.7 and 10-16.5 mol/m2/s. The process of alpha-recoilenrichment, while primarily responsible for the observed variation in(234U/238U) of natural systems, is difficult to quantify. However, therate of this process in natural systems affects the interpretation ofmost U-series data. Models for quantifying the alpha-recoil loss fractionbased on geometric predictions, surface area constraints, and chemicalmethods are also presented. The agreement between the chemical andtheoretical methods, such as direct measurement of (234U/238U) of thesmall grain size fraction and geometric calculations for that sizefraction, is quite good.

  10. Uranium Isotope Evidence for Temporary Ocean Oxygenation Following the Sturtian Glaciation

    Science.gov (United States)

    Lau, K. V.; Maher, K.; Macdonald, F. A.; Payne, J.

    2015-12-01

    The link between widespread ocean oxygenation in the Neoproterozoic and the rise of animals has long been debated, largely because the timing and nature of oxygenation of the oceans remain poorly constrained. Strata deposited during the Cryogenian non-glacial interlude (660 to 635 Ma), between the Sturtian and Marinoan Snowball Earth glaciations, contain the earliest fossil evidence of animals. To quantitatively estimate patterns of seafloor oxygenation during this critical interval, we present uranium isotope (δ238U) data from limestone of the Taishir Formation (Fm) in Mongolia in two stratigraphic sections that are separated by ~75 km across the basin. The Taishir Fm hosts two large δ13C excursions that co-vary in total organic and inorganic (carbonate) carbon: a basal carbonate δ13C excursion to -4‰ in the Sturtian cap carbonate, followed by a rise to enriched values of +8‰, a second negative δ13C excursion to -7‰ referred to as the Taishir excursion, followed by a second rise to +10‰. Above the Sturtian glacial deposits, in the stratigraphic interval below the Taishir excursion, δ238U compositions have a mean value that is similar to that of modern seawater. After the Taishir excursion, the δ238U record exhibits a step decrease of ~0.3‰, and δ238U remains approximately constant until the erosional unconformity at the base of the Marinoan glacial deposits. We use a box model to constrain the uranium cycle behavior that best explains our observations. In the model, the best explanation for the less negative post-Sturtian values of δ238U is extensive oxygenation of the seafloor. Moreover, the model demonstrates that the higher δ238U values of the post-Sturtian limestones are inconsistent with an increased flux of uranium to the oceans due to post-Snowball weathering as the primary driver of the excursion. Thus, we favor a scenario in which there was a rise in oxygen levels following the Sturtian glaciation followed by a decrease in seafloor

  11. Determination of uranium isotopic composition and {sup 236}U content of soil samples and hot particles using inductively coupled plasma mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Boulyga, S.F. [Radiation Physics and Chemistry Problems Inst., Minsk (Belarus); Becker, J.S. [Central Department for Analytical Chemistry, Research Centre Juelich (Germany)

    2001-07-01

    As a result of the accident at the Chernobyl nuclear power plant (NPP) the environment was contaminated with spent nuclear fuel. The {sup 236}U isotope was used in this study to monitor the spent uranium from nuclear fallout in soil samples collected in the vicinity of the Chernobyl NPP. Nuclear track radiography was applied for the identification and extraction of hot radioactive particles from soil samples. A rapid and sensitive analytical procedure was developed for uranium isotopic ratio measurement in environmental samples based on double-focusing inductively coupled plasma mass spectrometry (DF-ICP-MS) with a MicroMist nebulizer and a direct injection high-efficiency nebulizer (DIHEN). The performance of the DF-ICP-MS with a quartz DIHEN and plasma shielded torch was studied. Overall detection efficiencies of 4 x 10{sup -4} and 10{sup -3} counts per atom were achieved for {sup 238}U in DF-ICP-QMS with the MicroMist nebulizer and DIHEN, respectively. The rate of formation of uranium hydride ions UH{sup +}/U{sup +} was 1.2 x 10{sup -4} and 1.4 x 10{sup -4}, respectively. The precision of short-term measurements of uranium isotopic ratios (n = 5) in 1 {mu}g L{sup -1} NBS U-020 standard solution was 0.11% ({sup 238}U/{sup 235}U) and 1.4% ({sup 236}U/{sup 238}U) using a MicroMist nebulizer and 0.25% ({sup 235}U/{sup 238}U) and 1.9% ({sup 236}U/{sup 238}U) using a DIHEN. The isotopic composition of all investigated Chernobyl soil samples differed from those of natural uranium; i.e. in these samples the {sup 236}U/{sup 238}U ratio ranged from 10{sup -5} to 10{sup -3}. Results obtained with ICP-MS, {alpha}- and {gamma}-spectrometry showed differences in the migration properties of spent uranium, plutonium, and americium. The isotopic ratio of uranium was also measured in hot particles extracted from soil samples. (orig.)

  12. Natural radioactivity measurements in agricultural soil, fertilizer and crops in some specific areas of Kingdom of Saudi Arabia

    Energy Technology Data Exchange (ETDEWEB)

    Latif, Shaikh Abdul; Kinsara, Abdulraheem Abdulrahman; Molla, Nurul Islam; Nassef, Mohamed Hamed [King Abdulaziz Univ., Jeddah (Saudi Arabia). Faculty of Engineering

    2014-09-01

    High Purity Germanium (HPGe) detector gamma-ray spectrometry with 500 cc Marinelli beaker geometry was used for radioactivity measurement in some specific areas of Kingdom of Saudi Arabia (KSA). The detection limits of {sup 210}Pb, {sup 238}U, {sup 226}Ra, {sup 232}Th and {sup 40}K in soil, fertilizers, and vegetables lie mostly below 1 Bq/kg. The activity concentrations of {sup 238}U and {sup 226}Ra in local phosphate fertilizers were measured in the range of 236.8-879.0 Bq/kg and 101.5-297.0 Bq/kg, respectively. The respective activity concentrations of {sup 238}U and {sup 226}Ra measured in one charge of German phosphate fertilizer are in the range of 552.7-790.0 Bq/kg and 280.6-317.0 Bq/kg. The activity concentrations of {sup 232}Th are assessed to have maximum values up to 2.24 Bq/kg in locally manufactured phosphate fertilizers. Local urea exhibited concentration level (Bq/kg) of {sup 210}Pb, {sup 238}U, {sup 226}Ra, {sup 232}Th and {sup 40}K below the detection limit. Mean values of activity concentrations of {sup 238}U in agricultural soil of Wadi Fatima, Taif, Hada Al-Sham, Madina City and Abyar Al-MashiMadina are 21.7 ± 3.24, 38.2 ± 4.1, 17.6 ± 2.1, 34.3 ± 3.5 and 32.7 ± 2.4 Bq/kg, respectively. The respective mean of {sup 226}Ra activity concentrations in those areas are 12.16 ± 1.16, 20.2 ± 1.33, 11.21 ± 0.4, 21.4 ± 1.7 and 21.0 ± 1.22 Bq/kg. The specific activity of {sup 232}Th in the respective areas has been measured as 12.6 ± 1.3, 25.3 ± 0.8, 11.5 ± 0.9, 20.4 ± 2.4 and 20.0 ± 1.2 Bq/kg. Activity concentrations of {sup 210}Pb, {sup 238}U, {sup 226}Ra and {sup 232}Th in the vegetable samples are mostly found in the range of 0.37 Bq/kg to 37.8 Bq/kg. The {sup 40}K specific activity lies in the range of 44.4-196 Bq/kg. The calculated absorbed dose rates in the representative locations are 24.07-53.28 nGy/h. (orig.)

  13. Modern Measurements of Uranium Decay Rates

    Science.gov (United States)

    Parsons-Moss, T.; Faye, S. A.; Williams, R. W.; Wang, T. F.; Renne, P. R.; Mundil, R.; Harrison, M.; Bandong, B. B.; Moody, K.; Knight, K. B.

    2015-12-01

    It has been widely recognized that accurate and precise decay constants (λ) are critical to geochronology as highlighted by the EARTHTIME initiative, particularly the calibration benchmarks λ235U and λ238U. [1] Alpha counting experiments in 1971[2] measured λ235U and λ238U with ~0.1% precision, but have never been independently validated. We are embarking on new direct measurements of λ235U, λ238U, λ234Th, and λ234U using independent approaches for each nuclide. For the measurement of λ235U, highly enriched 235U samples will be chemically purified and analyzed for U concentration and isotopic composition by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). Thin films will be electrodeposited from these solutions and the α activity will be measured in an α-γ coincidence counting apparatus, which allows reduced uncertainty in counting efficiency while achieving adequate counting statistics. For λ238U measurement we will measure ingrowth of 234Th in chemically purified, isotopically enriched 238U solutions, by quantitatively separating the Th and allowing complete decay to 234U. All of the measurements will be done using MC-ICP-MS aiming at 0.05% precision. This approach is expected to result in values of λ238U with less than 0.1% uncertainty, if combined with improved λ234Th measements. These will be achieved using direct decay measurements with an E-∆E charged particle telescope in coincidence with a gamma detector. This system allows measurement of 234Th β-decay and simultaneous detection and identification of α particles emitted by the 234U daughter, thus observing λ234U at the same time. The high-precision λ234U obtained by the direct activity measurements can independently verify the commonly used values obtained by indirect methods.[3] An overarching goal of the project is to ensure the quality of results including metrological traceability in order to facilitate implementation across diverse disciplines. [1] T

  14. U-Th-Ra variations in Himalayan river sediments (Gandak river, India): Weathering fractionation and/or grain-size sorting?

    Science.gov (United States)

    Bosia, Clio; Chabaux, François; Pelt, Eric; France-Lanord, Christian; Morin, Guillaume; Lavé, Jérôme; Stille, Peter

    2016-11-01

    Understanding the origin of U-Th-Ra variations in the Ganga river sediments is a prerequisite for correctly using U-series nuclides to constrain the sediment transport times in Himalayan rivers. For this purpose, U, Th, and Ra concentrations, along with 238U-234U-230Th-226Ra radioactive disequilibria, were analyzed in bank, bedload and suspended sediments from the Gandak river, one of the main tributaries of the Ganga river. The data confirm that U and Th budgets of the Himalayan sediments are significantly influenced by minor resistant minerals, such as zircon, garnet and Ti-bearing minerals, the dissolution of which required the use of a high-pressure acid digestion process. Most importantly, the results indicate that the variations in (238U/232Th) and (230Th/232Th) activity ratios and 238U-234U-230Th-226Ra disequilibria in sediments along the river alluvial plain mainly reflect modifications in the mineralogical and grain-size compositions rather than the degree of weathering during transport. The (238U/232Th) and (230Th/232Th) activity ratios in the bank and bed sediments are related to variations in the minor primary minerals strongly enriched in U and Th (i.e., zircon, REE-bearing minerals and Ti-bearing minerals), whereas the activity ratios in the suspended load are related to variations in the proportions of clay, Fe-oxyhydroxides and the silt-sand fraction, which contains U- and Th-bearing minor minerals. The data also indicate that 238U-234U-230Th-226Ra disequilibria are strongly influenced by secondary mineral phases: the 230Th budget is likely mainly controlled by Fe-oxyhydroxides, and the 226Ra budget is likely mainly controlled by clay minerals. Therefore, the variations in the 238U-234U-230Th-232Th system in the sediments of the Gandak river cannot simply be interpreted as the result of fractionation due to chemical transformation of the bulk sediment during its transport within the alluvial plain and/or the result of radioactive decay. Consequently

  15. Natural fractionation of uranium isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Noordmann, Janine

    2015-01-24

    The topic of this thesis was the investigation of U (n({sup 238}U) / n({sup 235}U)) isotope variations in nature with a focus on samples (1) that represent the continental crust and its weathering products (i.e. granites, shales and river water) (2) that represent products of hydrothermal alteration on mid-ocean ridges (i.e. altered basalts, carbonate veins and hydrothermal water) and (3) from restricted euxinic basins (i.e. from the water column and respective sediments). The overall goal was to explore the environmental conditions and unravel the mechanisms that fractionate the two most abundant U isotopes, n({sup 238}U) and n({sup 235}U), on Earth.

  16. Thresholds on star formation and the chemical evolution of galactic discs cosmochronology and the age of the galaxy

    CERN Document Server

    Chamcham, K

    1995-01-01

    In this paper we analyse different chronometers based on the models of chemical evolution developed in Chamcham, Pitts \\& Tayler (1993; hereafter CPT) and Chamcham \\& Tayler (1994; hereafter CT). In those papers we discussed the ability of our models to reproduce the observed G-dwarf distribution in the solar neighbourhood, age-metallicity relation and radial chemical abundance gradients. We now examine their response to the predictions of cosmochronology. We use the recent production ratios of the actinide pairs ^{235}U/^{238}U and ^{232}Th/^{238}U provided by Cowan, Thielemann \\& Truran (1991) and the observed abundance ratios from Anders \\& Grevesse (1989) to determine the duration of nucleosynthesis in the solar neighbourhood, and thus to determine maximum likelihood estimates and confidence intervals for the infall parameter, \\beta, which controls the growth rate of the disc in our models. We compare our predictions for the age of the disc with the age of the galaxy estimated from models ...

  17. Evaluation of effective dose in consequence of Para chestnut ingestion; Avaliacao da dose efetiva em consequencia da ingestao de castanha do Para

    Energy Technology Data Exchange (ETDEWEB)

    Bellintani, Sandra A.; Oliveira, Joselens de; Carvalho, Jurandyr S. de; Hiromoto, Goro [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)

    1995-12-31

    Commercial samples of Brazil nut tree seed (Bertholletia excelsa) were analysed for the presence or uranium and thorium series of natural radionuclides. The samples were analysed for the content of {sup 238} U, {sup 226} Ra, {sup 210} Pb, {sup 232} Th, {sup 228} Th. Mean values 1.4 {+-} 0.4 Bq/kg for {sup 238} U, 26.3{+-}4.1 Bq/kG for {sup 226} Ra, 4.7{sup {+-}}1.8 Bq/kg for {sup 210} Pb, 16.5{+-}4.3 Bq/kg for {sup 232} Th, 31.3{+-}6.4 Bq/Kg for {sup 228} Ra and 12.3{+-}5.1 Bq/kg for {sup 228} Th. The effective dose due to the ingestion of natural radionuclides contained in the Brazil nuts, is 2.6 x 10{sup -2} mSv/kg ingested per year. (author). 9 refs., 1 tab.

  18. Multigroup covariance matrices for fast-reactor studies

    Energy Technology Data Exchange (ETDEWEB)

    Smith, J.D. III; Broadhead, B.L.

    1981-04-01

    This report presents the multigroup covariance matrices based on the ENDF/B-V nuclear data evaluations. The materials and reactions have been chosen according to the specifications of ORNL-5517. Several cross section covariances, other than those specified by that report, are included due to the derived nature of the uncertainty files in ENDF/B-V. The materials represented are Ni, Cr, /sup 16/O, /sup 12/C, Fe, Na, /sup 235/U, /sup 238/U, /sup 239/Pu, /sup 240/Pu, /sup 241/Pu, and /sup 10/B (present due to its correlation to /sup 238/U). The data have been originally processed into a 52-group energy structure by PUFF-II and subsequently collapsed to smaller subgroup strutures. The results are illustrated in 52-group correlation matrix plots and tabulated into thirteen groups for convenience.

  19. Certified reference materials for radionuclides in Bikini Atoll sediment (IAEA-410) and Pacific Ocean sediment (IAEA-412).

    Science.gov (United States)

    Pham, M K; van Beek, P; Carvalho, F P; Chamizo, E; Degering, D; Engeler, C; Gascó, C; Gurriaran, R; Hanley, O; Harms, A V; Herrmann, J; Hult, M; Ikeuchi, Y; Ilchmann, C; Kanisch, G; Kis-Benedek, G; Kloster, M; Laubenstein, M; Llaurado, M; Mas, J L; Nakano, M; Nielsen, S P; Osvath, I; Povinec, P P; Rieth, U; Schikowski, J; Smedley, P A; Suplinska, M; Sýkora, I; Tarjan, S; Varga, B; Vasileva, E; Zalewska, T; Zhou, W

    2016-03-01

    The preparation and characterization of certified reference materials (CRMs) for radionuclide content in sediments collected offshore of Bikini Atoll (IAEA-410) and in the open northwest Pacific Ocean (IAEA-412) are described and the results of the certification process are presented. The certified radionuclides include: (40)K, (210)Pb ((210)Po), (226)Ra, (228)Ra, (228)Th, (232)Th, (234)U, (238)U, (239)Pu, (239+240)Pu and (241)Am for IAEA-410 and (40)K, (137)Cs, (210)Pb ((210)Po), (226)Ra, (228)Ra, (228)Th, (232)Th, (235)U, (238)U, (239)Pu, (240)Pu and (239+240)Pu for IAEA-412. The CRMs can be used for quality assurance and quality control purposes in the analysis of radionuclides in sediments, for development and validation of analytical methods and for staff training. Copyright © 2015 Elsevier Ltd. All rights reserved.

  20. Theoretical predictions on production of neutron-deficient nuclei with Z ≥ 93 in multinucleon transfer reactions

    Science.gov (United States)

    Zhu, Long; Su, Jun; Zhang, Feng-Shou

    2017-08-01

    Within the framework of dinuclear system model, the transfer reactions 58Ni + 233U, 58Ni + 238U, and 64Ni + 238U are investigated. The influences of projectile and target neutron numbers on cross sections of producing neutron-deficient actinide nuclei in transfer reactions are studied. It is found that the system 58Ni + 233U with smaller neutron excess is favorable to produce neutron-deficient nuclei. We predict the production cross sections of neutron-deficient nuclei with Z = 93- 98 in transfer reactions 58Ni + 233U and 40Ca + 245Cm with different incident energies. We find the transfer reactions 58Ni + 233U and 40Ca + 245Cm are feasible for producing neutron-deficient actinide nuclei in future experiments.

  1. Monte Carlo simulation of γ and fission transfer-induced probabilities using extended ?-matrix theory: Application to the 237U∗ system

    Science.gov (United States)

    Bouland, Olivier; Jurado, Beatriz

    2017-09-01

    This paper deals with simultaneous neutron-induced average partial cross sections and surrogate-like probability simulations over several excitation and de-excitation channels of the compound nucleus. Present calculations, based on one-dimensional fission barrier extended ?-matrix theory using Monte Carlo samplings of both first and second well resonance parameters, avoid the surrogate-reaction method historically taken for surrogate data analyses that proved to be very poor in terms of extrapolated neutron-induced capture cross sections. Present theoretical approach is portrayed and subsequent results can be compared for the first time with experimental γ-decay probabilities; thanks to brand new simultaneous 238U(3He,4Heγ) and 238U(3He,4He f) surrogate measurements. Future integration of our strategy in standard neutron cross section data evaluation remains tied to the developments made in terms of direct reaction population probability calculations.

  2. Evaluation of radioactive emissions of lignite-fired power plants in Turkey using the Analytic Hierarchy Process

    Energy Technology Data Exchange (ETDEWEB)

    Bueke, Tayfun [Mugla Sitki Kocman Univ., Mugla (Turkey). Dept. of Energy Systems Engineering

    2013-11-15

    Radioactive emissions of 13 lignite-fired power plants in Turkey are of great concern to the public and to scientists alike. The purpose of this study is to evaluate these power plants, according to their radioactive emissions by using the Analytic Hierarchy Process. Control criteria are in particular {sup 226}Ra, {sup 232}Th, {sup 40}K and {sup 238}U emissions from the power plants. These control criteria are weighted according to the objective assessment. The calculations are repeated for three different objective assessments of control criteria namely the mortality risk coefficients for inhalation, ingestion, external exposure of {sup 226}Ra, {sup 232}Th, {sup 40}K and {sup 238}U. It has been calculated that the Can lignite-fired power plant is ranking first while the Soma-B plant is ranking last according to the radioactive emissions of the power plants when the average of three different objective control criteria are used in the calculations. (orig.)

  3. Sequential Injection Method for Rapid and Simultaneous Determination of 236U, 237Np, and Pu Isotopes in Seawater

    DEFF Research Database (Denmark)

    Qiao, Jixin; Hou, Xiaolin; Steier, Peter;

    2013-01-01

    An automated analytical method implemented in a novel dual-column tandem sequential injection (SI) system was developed for simultaneous determination of 236U, 237Np, 239Pu, and 240Pu in seawater samples. A combination of TEVA and UTEVA extraction chromatography was exploited to separate and purify...... target analytes, whereupon plutonium and neptunium were simultaneously isolated and purified on TEVA, while uranium was collected on UTEVA. The separation behavior of U, Np, and Pu on TEVA–UTEVA columns was investigated in detail in order to achieve high chemical yields and complete purification...... for the radionuclides of interest. 242Pu was used as a chemical yield tracer for both plutonium and neptunium. 238U was quantified in the sample before the separation for deducing the 236U concentration from the measured 236U/238U atomic ratio in the separated uranium target using accelerator mass spectrometry...

  4. Sensitivity of computed uranium-238 self-shielding factors to the choice of the unresolved average resonance parameters

    Energy Technology Data Exchange (ETDEWEB)

    Munoz-Cobos, J.L.; de Saussure, G.; Perez, R.B.

    1982-05-01

    The influence of different representations of the unresolved resonances of /sup 238/U on the computed self-shielding factors is examined. It is shown that the evaluated infinitely diluted average capture cross section does not provide sufficient information to determine a unique set of unresolved resonance parameters; different sets of unresolved resonance parameters equally consistent with the evaluated average capture cross section yield significantly different computed self-shielding factors. In the conclusion it is recommended that the resolved resonance description of the evaluated /sup 238/U cross sections be extended to higher energies and that thick sample transmission data and self-indication data be used to improve the evaluation of the unresolved resonance region.

  5. Isotopic characterization of uranium in soils of the Ipanema National Forest (FLONA-Ipanema); Caracterizacao isotopica de uranio em solos da Floresta Nacional de Ipanema (FLONA-Ipanema)

    Energy Technology Data Exchange (ETDEWEB)

    Silva, F.B.; Marques, F.H., E-mail: fernandobaliani@yahoo.com.br, E-mail: fernando_henrique06@hotmail.com [Laboratorio de Pocos de Caldas (LAPOC/CNEN-MG), Pocos de Caldas, MG (Brazil); Enzweiler, J.; Ladeira, F.S.B., E-mail: Jacinta@ige.unicamp.br, E-mail: fsbladeira@ige.unicamp.br [Universidade Estadual de Campinas (UNICAMP), Campinas, SP (Brazil). Instituto de Geociencias

    2015-07-01

    The National Forest of Ipanema (FLONA) is situated on a geological anomaly, known as 'Domo de Aracoiaba'. The soils of the area include Oxisols, Inceptsols and Alfisols. The amount of uranium and respective isotope activities in a soil depend on the parental rock and on the pedologic processes. The aim of this study was to investigate the activities for uranium isotopes ({sup 238}U, {sup 234}U, {sup 235}U) and the activity ratio (AR) {sup 234}U/ {sup 238}U or secular equilibrium for different soil types of the area collected at horizons A and B. The amount of uranium showed no significant differences for soils generated from alkaline intrusive rocks and sandstone, however, secular equilibrium was observed for Oxisol (RA = 1), while Inceptsol presented RA> 1 and the other soils, Alfisols, presented RA values <1. (author)

  6. The simultaneous neutron and photon interrogation method for fissile and non-fissile element separation in radioactive waste drums

    Energy Technology Data Exchange (ETDEWEB)

    Jallu, F. E-mail: fanny.jallu@cea.fr; Lyoussi, A.; Passard, C.; Payan, E.; Recroix, H.; Nurdin, G.; Buisson, A.; Allano, J

    2000-10-01

    Measuring {alpha}-emitters such as ({sup 234,235,236,238}U, {sup 238,239,240,242,244}Pu, {sup 237}Np, {sup 241,243}Am, ...), in solid radioactive waste allows us to quantify the {alpha}-activity in a drum and then to classify it. The simultaneous photon and neutron interrogation experiment (SIMPHONIE) method dealt with in this paper, combines both active neutron interrogation and induced photofission interrogation techniques simultaneously. Its purpose is to quantify fissile ({sup 235}U, {sup 239,241}Pu, ...) and non-fissile ({sup 236,238}U, {sup 238,240}Pu, ...) elements separately in only one measurement. This paper presents the principle of the method, the experimental setup, and the first experimental results obtained using the DGA/ETCA Linac and MiniLinatron pulsed linear electron accelerators located at Arcueil, France. First studies were carried out with U and Pu bare samples.

  7. Uranium isotopic data in uraninite spent fuel from the Bangombe natural nuclear reactor (Gabon) and its surroundings

    Science.gov (United States)

    Fernandez-Diaz; Quejido; Crespo; Perez del Villar L; Martin-Sanchez; Lozano

    2000-07-01

    In the framework of the "Oklo-Natural Analogue Phase II" Project, uraninite from the Bangombe natural reactor and samples from its host rock were analyzed to determine their uranium isotopic composition by thermal ionisation mass spectrometry, inductively coupled plasma mass spectrometry and alpha spectrometry. There were several objectives for this work: (i) to validate the 235U/238U isotopic ratios obtained by these techniques; (ii) to test the use of the 235U/238U ratio of uraninite as a tracer of migration/retention processes of uranium from the source term to the far field; (iii) to evaluate the most recent migration/retention processes of uranium in the system by U-series disequilibrium.

  8. Uranium isotopic data in uraninite spent fuel from the Bangombe natural nuclear reactor (Gabon) and its surroundings

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez-Diaz, M.; Quejido, A.J.; Crespo, M.T.; Villar, L.P. del; Martin-Sanchez, A. E-mail: ams@unex.es; Lozano, J.C

    2000-07-15

    In the framework of the 'Oklo-Natural Analogue Phase II' Project, uraninite from the Bangombe natural reactor and samples from its host rock were analyzed to determine their uranium isotopic composition by thermal ionisation mass spectrometry, inductively coupled plasma mass spectrometry and alpha spectrometry. There were several objectives for this work: (i) to validate the {sup 235}U/{sup 238}U isotopic ratios obtained by these techniques; (ii) to test the use of the {sup 235}U/{sup 238}U ratio of uraninite as a tracer of migration/retention processes of uranium from the source term to the far field; (iii) to evaluate the most recent migration/retention processes of uranium in the system by U-series disequilibrium.

  9. Application of FORSS sensitivity and uncertainty methodology to fast reactor benchmark analysis

    Energy Technology Data Exchange (ETDEWEB)

    Weisbin, C.R.; Marable, J.H.; Lucius, J.L.; Oblow, E.M.; Mynatt, F.R.; Peelle, R.W.; Perey, F.G.

    1976-12-01

    FORSS is a code system used to study relationships between nuclear reaction cross sections, integral experiments, reactor performance parameter predictions, and associated uncertainties. This paper presents the theory and code description as well as the first results of applying FORSS to fast reactor benchmarks. Specifically, for various assemblies and reactor performance parameters, the nuclear data sensitivities were computed by nuclide, reaction type, and energy. Comprehensive libraries of energy-dependent coefficients have been developed in a computer retrievable format and released for distribution by RSIC and NNCSC. Uncertainties induced by nuclear data were quantified using preliminary, energy-dependent relative covariance matrices evaluated with ENDF/B-IV expectation values and processed for /sup 238/U(n,f), /sup 238/U(n,..gamma..), /sup 239/Pu(n,f), and /sup 239/Pu(..nu..). Nuclear data accuracy requirements to meet specified performance criteria at minimum experimental cost were determined.

  10. On the search for a (n,f cross-section reference at intermediate energies

    Directory of Open Access Journals (Sweden)

    Duran I.

    2017-01-01

    Full Text Available The (n,f cross-sections proposed as references by the IAEA for 235U, 238U and 209Bi are compared with a new analysis that combines the measurements performed at CERN-n_TOF of their cross-section ratios with new calculations done using Monte Carlo codes based on phenomenological models INCL+ +, GEMINI+ +, and ABLA07. The calculations are cross-checked with those for the (p,f reactions, where experimental values are available. We have evaluated in this way the (n,f cross sections for 238U, 235U and 209Bi, in the intermediate energy region going from 190 MeV to 2 GeV. Our results definitively discard the JENDL/HE-2007 evaluations above 300 MeV, falling inside the confidence corridor proposed by IAEA but for the points around 300–400 MeV where a discrepancy is to be noticed.

  11. Limits on uranium and thorium bulk content in GERDA Phase I detectors

    CERN Document Server

    Agostini, M; Bakalyarov, A M; Balata, M; Barabanov, I; Baudis, L; Bauer, C; Becerici-Schmidt, N; Bellotti, E; Belogurov, S; Belyaev, S T; Benato, G; Bettini, A; Bezrukov, L; Bode, T; Borowicz, D; Brudanin, V; Brugnera, R; Caldwell, A; Cattadori, C; Chernogorov, A; D'Andrea, V; Demidova, E V; di Vacri, A; Domula, A; Doroshkevich, E; Egorov, V; Falkenstein, R; Fedorova, O; Freund, K; Frodyma, N; Gangapshev, A; Garfagnini, A; Grabmayr, P; Gurentsov, V; Gusev, K; Hakemüller, J; Hegai, A; Heisel, M; Hemmer, S; Hofmann, W; Hult, M; Inzhechik, L V; Csathy, J Janicsko; Jochum, J; Junker, M; Kazalov, V; Kihm, T; Kirpichnikov, I V; Kirsch, A; Kish, A; Klimenko, A; Kneißl, R; Knöpfle, K T; Kochetov, O; Kornoukhov, V N; Kuzminov, V V; Laubenstein, M; Lazzaro, A; Lebedev, V I; Lehnert, B; Liao, H Y; Lindner, M; Lippi, I; Lubashevskiy, A; Lubsandorzhiev, B; Lutter, G; Macolino, C; Majorovits, B; Maneschg, W; Medinaceli, E; Mingazheva, R; Misiaszek, M; Moseev, P; Nemchenok, I; Palioselitis, D; Panas, K; Pandola, L; Pelczar, K; Pullia, A; Riboldi, S; Rumyantseva, N; Sada, C; Salamida, F; Salathe, M; Schmitt, C; Schneider, B; Schönert, S; Schreiner, J; Schütz, A -K; Schulz, O; Schwingenheuer, B; Selivanenko, O; Shevchik, E; Shirchenko, M; Simgen, H; Smolnikov, A; Stanco, L; Stepaniuk, M; Vanhoefer, L; Vasenko, A A; Veresnikova, A; von Sturm, K; Wagner, V; Walter, M; Wegmann, A; Wester, T; Wiesinger, C; Wojcik, M; Yanovich, E; Zhitnikov, I; Zhukov, S V; Zinatulina, D; Zuber, K; Zuzel, G

    2016-01-01

    Internal contaminations of $^{238}$U, $^{235}$U and $^{232}$Th in the bulk of high purity germanium detectors are potential backgrounds for experiments searching for neutrinoless double beta decay of $^{76}$Ge. The data from GERDA Phase~I have been analyzed for alpha events from the decay chain of these contaminations by looking for full decay chains and for time correlations between successive decays in the same detector. No candidate events for a full chain have been found. Upper limits on the activities in the range of a few nBq/kg for $^{226}$Ra, $^{227}$Ac and $^{228}$Th, the long-lived daughter nuclides of $^{238}$U, $^{235}$U and $^{232}$Th, respectively, have been derived. With these upper limits a background index in the energy region of interest from $^{226}$Ra and $^{228}$Th contamination is estimated which satisfies the prerequisites of a future ton scale germanium double beta decay experiment.

  12. Uranium and molybdenum isotope evidence for an episode of widespread ocean oxygenation during the late Ediacaran Period

    Science.gov (United States)

    Kendall, Brian; Komiya, Tsuyoshi; Lyons, Timothy W.; Bates, Steve M.; Gordon, Gwyneth W.; Romaniello, Stephen J.; Jiang, Ganqing; Creaser, Robert A.; Xiao, Shuhai; McFadden, Kathleen; Sawaki, Yusuke; Tahata, Miyuki; Shu, Degan; Han, Jian; Li, Yong; Chu, Xuelei; Anbar, Ariel D.

    2015-05-01

    To improve estimates of the extent of ocean oxygenation during the late Ediacaran Period, we measured the U and Mo isotope compositions of euxinic (anoxic and sulfidic) organic-rich mudrocks (ORM) of Member IV, upper Doushantuo Formation, South China. The average δ238U of most samples is 0.24 ± 0.16‰ (2SD; relative to standard CRM145), which is slightly higher than the average δ238U of 0.02 ± 0.12‰ for restricted Black Sea (deep-water Unit I) euxinic sediments and is similar to a modeled δ238U value of 0.2‰ for open ocean euxinic sediments in the modern well-oxygenated oceans. Because 238U is preferentially removed to euxinic sediments compared to 235U, expanded ocean anoxia will deplete seawater of 238U relative to 235U, ultimately leading to deposition of ORM with low δ238U. Hence, the high δ238U of Member IV ORM points to a common occurrence of extensive ocean oxygenation ca. 560 to 551 Myr ago. The Mo isotope composition of sediments deposited from strongly euxinic bottom waters ([H2S]aq >11 μM) either directly records the global seawater Mo isotope composition (if Mo removal from deep waters is quantitative) or represents a minimum value for seawater (if Mo removal is not quantitative). Near the top of Member IV, δ98Mo approaches the modern seawater value of 2.34 ± 0.10‰. High δ98Mo points to widespread ocean oxygenation because the preferential removal of isotopically light Mo to sediments occurs to a greater extent in O2-rich compared to O2-deficient marine environments. However, the δ98Mo value for most Member IV ORM is near 0‰ (relative to standard NIST SRM 3134 = 0.25‰), suggesting extensive anoxia. The low δ98Mo is at odds with the high Mo concentrations of Member IV ORM, which suggest a large seawater Mo inventory in well-oxygenated oceans, and the high δ238U. Hence, we propose that the low δ98Mo of most Member IV ORM was fractionated from contemporaneous seawater. Possible mechanisms driving this isotope fractionation include

  13. Fission fragment mass distributions via prompt -ray spectroscopy

    Indian Academy of Sciences (India)

    L S Danu; D C Biswas; B K Nayak; R K Choudhury

    2015-09-01

    The distribution of fragment masses formed in nuclear fission is one of the most striking features of the process. Such measurements are very important to understand the shape evolution of the nucleus from ground state to scission through intermediate saddle points. The fission fragment mass distributions, generally obtained via conventional methods (i.e., by measuring the energy and/or the velocity of the correlated fission fragments) are limited to a mass resolution of 4–5 units. On the other hand, by employing the -ray spectroscopy, it is possible to estimate the yield of individual fission fragments. In this work, determination of the fission fragment mass distribution by employing prompt -ray spectroscopy is described along with the recent results on 238U(18O, f) and 238U(32S, f) systems.

  14. Determination of {sup 233}U by inductively coupled argon plasma - atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Patwardhan, A.B.; Kulkarni, V.T.; Radhakrishnan, K.; Ramanujam, A.; Page, A.G. [Bhabha Atomic Research Centre, Bombay (India)

    1994-09-01

    The paper describes studies carried out for the determination of {sup 233}U at various stages during the recovery and purification of {sup 233}U from {sup 233}U-Al alloy scraps generated during the fabrication of {sup 233}U-Al alloy fuel. Employing a high resolution sequential spectrometer and Inductively Coupled argon Plasma (ICP) as the spectral excitation source, isotope shift for {sup 233}U with respect to {sup 238}U has been resolved and recorded. The shift for the 424.437 nm emission line of {sup 238}U is found to be of the order of 0.040 nm on the lower wavelength side for {sup 233}U and this isotopic effect has been utilised for the quantitative determination of {sup 233}U. The overall precision of the method is 5% RSD with the detection limit of 0.01 {mu}g/ml.

  15. Method for radioactivity monitoring

    Science.gov (United States)

    Umbarger, C. John; Cowder, Leo R.

    1976-10-26

    The disclosure relates to a method for analyzing uranium and/or thorium contents of liquid effluents preferably utilizing a sample containing counting chamber. Basically, 185.7-keV gamma rays following .sup.235 U alpha decay to .sup.231 Th which indicate .sup.235 U content and a 63-keV gamma ray doublet found in the nucleus of .sup.234 Pa, a granddaughter of .sup.238 U, are monitored and the ratio thereof taken to derive uranium content and isotopic enrichment .sup.235 U/.sup.235 U + .sup.238 U) in the liquid effluent. Thorium content is determined by monitoring the intensity of 238-keV gamma rays from the nucleus of .sup.212 Bi in the decay chain of .sup.232 Th.

  16. Statistical modelling of neural networks in {gamma}-spectrometry applications

    Energy Technology Data Exchange (ETDEWEB)

    Vigneron, V.; Martinez, J.M. [CEA Centre d`Etudes de Saclay, 91 - Gif-sur-Yvette (France). Dept. de Mecanique et de Technologie; Morel, J.; Lepy, M.C. [CEA Centre d`Etudes de Saclay, 91 - Gif-sur-Yvette (France). Dept. des Applications et de la Metrologie des Rayonnements Ionisants

    1995-12-31

    Layered Neural Networks, which are a class of models based on neural computation, are applied to the measurement of uranium enrichment, i.e. the isotope ratio {sup 235} U/({sup 235} U + {sup 236} U + {sup 238} U). The usual method consider a limited number of {Gamma}-ray and X-ray peaks, and require previously calibrated instrumentation for each sample. But, in practice, the source-detector ensemble geometry conditions are critically different, thus a means of improving the above convention methods is to reduce the region of interest: this is possible by focusing on the K{sub {alpha}} X region where the three elementary components are present. Real data are used to study the performance of neural networks. Training is done with a Maximum Likelihood method to measure uranium {sup 235} U and {sup 238} U quantities in infinitely thick samples. (authors). 18 refs., 6 figs., 3 tabs.

  17. Radiochemical dates obtained by alpha spectrometry on fossil mollusk shell from the 5e Atlantic shoreline of the High Atlas, Morocco.

    Science.gov (United States)

    Choukri, A; Hakam, O-K; Reyss, J-L; Plaziat, J-C

    2007-08-01

    The reported radiochemical results obtained on 77 samples collected from Moroccan fossil beaches assumed to be deposited during the above present sea-level high stands corresponding to 5e climatic stage, and on 12 present and Holocene samples, are discussed in order to judge the age validity. Contrary to the Holocene shells where (238)U contents are low and (234)U/(238)U are in agreement with sea-water ratio, the 5e results vary considerably irrespective of species and calcite content of samples. Because of the open-system possibility, the (230)Th/(234)U ages based on shell samples should be interpreted as minima for any studied shoreline discussed in the light of geological data and several shells analyses.

  18. Mussels (Mytilus galloprovincialis) as a bio-indicator species in radioactivity monitoring of Eastern Adriatic coastal waters.

    Science.gov (United States)

    Krmpotić, Matea; Rožmarić, Martina; Barišić, Delko

    2015-06-01

    Croatian Adriatic coastal waters are systematically monitored within the Mediterranean Mussel Watch Project using mussels (Mytilus galloprovincialis) as a bio-indicator species. The study includes determination of naturally occurring ((7)Be, (40)K, (232)Th, (226)Ra and (238)U), as well as anthropogenic (137)Cs radionuclides. Activity concentrations in dry weight of mussels' soft tissue along the Croatian Adriatic coast are presented, with spatial and seasonal variations given and discussed. Samples were collected in spring and autumn for the period between 2009 and 2013. Radionuclides were determined by gamma-ray spectrometry. Activity concentrations of (7)Be were the highest in spring periods, especially in the areas with significant fresh water discharges. Activity concentrations of (40)K did not vary significantly with season or location. (137)Cs activities were low, while (232)Th, (226)Ra and (238)U activities were mostly below the detection limit of performed gamma-spectrometric measurement.

  19. Plutonium, (137)Cs and uranium isotopes in Mongolian surface soils.

    Science.gov (United States)

    Hirose, K; Kikawada, Y; Igarashi, Y; Fujiwara, H; Jugder, D; Matsumoto, Y; Oi, T; Nomura, M

    2017-01-01

    Plutonium ((238)Pu and (239,240)Pu), (137)Cs and plutonium activity ratios ((238)Pu/(239,240)Pu) as did uranium isotope ratio ((235)U/(238)U) were measured in surface soil samples collected in southeast Mongolia. The (239,240)Pu and (137)Cs concentrations in Mongolian surface soils (surface soils (0.013-0.06) coincided with that of global fallout. The (235)U/(238)U atom ratios in the surface soil show the natural one. There was a good correlation between the (239,240)Pu and (137)Cs concentrations in the surface soils. We introduce the migration depth to have better understanding of migration behaviors of anthropogenic radionuclides in surface soil. We found a difference of the migration behavior between (239,240)Pu and (137)Cs from (137)Cs/(239,240)Pu - (137)Cs plots for the Mongolian and Tsukuba surface soils; plutonium in surface soil is migrated easier than (137)Cs.

  20. Design optimization of the APF DTL in the SSC-linac

    Science.gov (United States)

    Wang, Zhi-Jun; He, Yuan; Wu, Wei; Yang, Ya-Qing; Xiao, Chen

    2010-10-01

    A linear accelerator as a new injector for the SSC (Separated Sector Cyclotron) of the HIRFL (Heavy Ion Research Facility Lanzhou) is being designed. The DTL (Drift-Tube-Linac) has been designed to accelerate 238U34+ from 0.140 MeV/u to 0.97 MeV/u. To the first accelerating tank which accelerates 238U34+ to 0.54 MeV/u, the approach of Alternating-Phase-Focusing (APF) is applied. The phase array is obtained by coupling optimization software Dakota and beam optics code LINREV. With the hybrid of Multi-objective Genetic Algorithm (MOGA) and a pattern search method, an optimum array of asynchronous phases is determined. The final growth, both transversely and longitudinally, can meet the design requirements. In this paper, the deign optimization of the APF DTL is presented.

  1. Angular anisotropy of the fusion-fission and quasifission fragments

    CERN Document Server

    Nasirov, A K; Utamuratov, R K; Fazio, G; Giardina, G; Hanappe, F; Mandaglio, G; Manganaro, M; Scheid, W

    2007-01-01

    The anisotropy in the angular distribution of the fusion-fission and quasifission fragments for the $^{16}$O+$^{238}$U, $^{19}$F+$^{208}$Pb and $^{32}$S+$^{208}$Pb reactions is studied by analyzing the angular momentum distributions of the dinuclear system and compound nucleus which are formed after capture and complete fusion, respectively. The orientation angles of axial symmetry axes of colliding nuclei to the beam direction are taken into account for the calculation of the variance of the projection of the total spin onto the fission axis. It is shown that the deviation of the experimental angular anisotropy from the statistical model picture is connected with the contribution of the quasifission fragments which is dominant in the $^{32}$S+$^{208}$Pb reaction. Enhancement of anisotropy at low energies in the $^{16}$O+$^{238}$U reaction is connected with quasifission of the dinuclear system having low temperature and effective moment of inertia.

  2. Measurement of the total activity concentrations of Libyan oil scale

    Science.gov (United States)

    Da Silva, F. C. A.; Bradley, D. A.; Regan, P. H.; Rozaila, Z. Siti

    2017-08-01

    Twenty-three oil scale samples obtained from the Libyan oil and gas industry production facilities onshore have been measured using high-resolution gamma-ray spectrometry with a shielded HPGe detector, the work being carried out within the Environmental Radioactivity Laboratory at the University of Surrey. The main objectives of this work were to determine the extent to which the predominant radionuclides associated with the uranium and thorium natural decay chains were in secular equilibrium with their decay progeny, also to compare differences between the total activity concentrations (TAC) in secular equilibrium and disequilibrium and to evaluate the measured activities for the predominant gamma-ray emitting decay radionuclides within the 232Th and 238U chains. The oil scale NORM samples did not exhibit radioactive equilibrium between the decay progeny and longer-lived parent radionuclides of the 238U and 232Th series.

  3. Multi-Nucleon Exchange in Quasi-Fission Reactions

    CERN Document Server

    Ayik, S; Yilmaz, O

    2015-01-01

    Nucleon exchange mechanism is investigated in the central collisions of ${}^{40}$Ca + ${}^{238}$U and ${}^{48}$Ca + ${}^{238}$U systems near the quasi-fission regime in the framework of the Stochastic Mean-Field (SMF) approach. Sufficiently below the fusion barrier, di-nuclear structure in the collisions is maintained to a large extend. Consequently, it is possible to describe nucleon exchange as a diffusion process familiar from deep-inelastic collisions. Diffusion coefficients for proton and neutron exchange are determined from the microscopic basis of the SMF approach in the semi-classical framework. Calculations show that after a fast charge equilibration the system drifts toward symmetry over a very long interaction time. Large dispersions of proton and neutron distributions of the produced fragments indicate that diffusion mechanism may help to populate heavy trans-uranium elements near the quasi-fission regime in these collisions.

  4. Using U-series Isotopes To Determine Sources Of Pedogenic Carbonates: Comparison Of Natural And Agricultural Soils In The Semi-arid Southern New Mexico And Western Texas

    Science.gov (United States)

    Nyachoti, S. K.; Ma, L.; Borrok, D. M.; Jin, L.; Tweedie, C. E.

    2012-12-01

    Pedogenic carbonates commonly precipitate from infiltrating soil water in arid and semi-arid lands and are observed in soils of southern New Mexico and western Texas. These carbonates could form an impermeable layer in the soil horizons impairing water infiltration, thus affecting crop growth and yield. It is important to determine the source of C and Ca in these carbonates and to understand conditions favoring their formation, kinetics and precipitation rates. In this study, major elements and U-series isotopes in bulk calcic soils, and weak acid leachates and residues were measured from one irrigated alfalfa site in the Hueco basin near El Paso, TX and one natural shrubland site on the USDA Jornada experimental range in southern NM. The combined geochemical and isotopic results allow us to determine the formation ages of the carbonates; investigate the mobility of U, Th, and major elements in these soils; and infer for the effects of irrigation on carbonate formation in agricultural soils. Our results show distinctive U and Th isotope systems in the two soil profiles analyzed. For example, (234U/238U) ratios in the Jornada bulk soils decrease from ~1.01 to 0.96 towards the surface, consistent with a preferential loss of 234U over 238U during chemical weathering. At the Jornada site, (238U/232Th) ratios decrease while (230Th/238U) increase towards the surface, consistent with a general depletion of U and the immobility of Th in the natural soils. By contrast at the Alfalfa site, (234U/238U) ratios of bulk soils increase from ~ 0.97 to 1.02 towards the surface, suggesting an additional source of external uranium, most likely the irrigation water from Rio Grande which has a (234U/238U) ratio of ~ 1.5 near El Paso. The (238U/232Th) and (230Th/238U) ratios also imply leaching of U from shallower soils but precipitation in greater depths at Alfalfa site; suggests that partial dissolution and re-precipitation of younger carbonates occur. Calculated carbonate ages from U

  5. Radiological Impact of Phosphogypsum Application in Agriculture

    Science.gov (United States)

    Dias, Nivea M. P.; Caires, Eduardo F.; Pires, Luiz F.; Bacchi, Marcio A.; Fernandes, Elisabete A. N.

    2010-08-01

    Phosphogypsum (PG) contains radionuclides from 238U and 232Th decay series. Due to the presence of these radionuclides, many countries restricted the use of PG in agriculture, however there is not such restriction in Brazil. The main objective of this work was to evaluate the impact of PG application on 226Ra (238U) and 228Ra (232Th) concentrations in soil. Gamma-spectrometry was carried out using HPGe detector. No increment of 226Ra and 228Ra was observed for increasing PG doses. Average values found for 226Ra and 228Ra were respectively 37 Bq kg-1 and 57 Bq kg-1. The results showed that the increasing PG doses in the specific conditions of the experiment did not cause a significant increment of radionuclides.

  6. Plutonium-244 fission xenon in the most primitive meteorites

    Energy Technology Data Exchange (ETDEWEB)

    Kuroda, P.K.; Myers, W.A. (Dept. of Chemical Engineering, Univ. Arkansas, Fayetteville, AR (United States))

    1994-01-01

    The plutonium-244/xenon-136 ages of the Murchison, Murray and Orgueil meteorites have been calculated from the existing xenon isotope data and the uranium contents. The CI carbonaceous chondrite Orgueil, which is considered to be among the most primitive - in the sense of the least altered - sample of the solar system known to man, appears to have started to retain its xenon more than 5,000 million years ago, when the ratio of [sup 244]Pu to [sup 238]U in the solar system was as high as (0.5 [+-] 0.1) (atom/atom) and the CM carbonaceous chondrites Murchison and Murray started to retain their xenon about 4,940 million years ago, when the [sup 244]Pu to [sup 238]U ratio was about 0.17 (atom/atom). (orig.)

  7. Radiological survey of the Shpack Landfill, Norton, Massachusetts

    Energy Technology Data Exchange (ETDEWEB)

    Cottrell, W.D.; Haywood, F.F.; Witt, D.A.; Myrick, T.E.; Goldsmith, W.A.; Shinpaugh, W.H.; Loy, E.T.

    1981-12-01

    The results of a radiological survey of the Shpack Landfill, Norton, Massachusetts, are given in this report. The survey was conducted over approximately eight acres which had received radioactive wastes from 1946 to 1965. The survey included measurement of the following: external gamma radiation at the surface and at 1 m (3 ft) above the surface throughout the site; beta-gamma exposure rates at 1 cm (0.4 in.) from the surface throughout the site; concentrations of /sup 226/Ra, /sup 238/U, and /sup 235/U in surface and subsurface soil on the site; and concentrations of /sup 226/Ra, /sup 238/U, /sup 235/U, /sup 230/Th, and /sup 210/Pb in groundwater on the site and in surface water on and near the site. Results indicate that the radioactive contamination is confined to the site and to the swamp immediately adjacent to the site.

  8. Photon and proton induced fission on heavy nuclei at intermediate energies

    Directory of Open Access Journals (Sweden)

    Andrade-II E.

    2014-04-01

    Full Text Available We present an analysis of fission induced by intermediate energy protons or photons on actinides. The 660 MeV proton induced reactions are on 241Am, 238U, and 237Np targets and the Bremmstrahlung-photons with end-point energies at 50 MeV and 3500 MeV are on 232Th and 238U targets. The study was performed by means of the Monte Carlo simulation code CRISP. A multimodal fission extension was added to the code within an approach which accounts for the contribution of symmetric and asymmetric fission. This procedure allowed the investigation of fission cross sections, fissility, number of evaporated nucleons and fission-fragment charge distributions. The comparison with experimental data show a good agreement between calculations and experiments.

  9. Revisiting the U-238 thermal capture cross section and gamma-raymission probabilities from Np-239 decay

    Energy Technology Data Exchange (ETDEWEB)

    Trkov, A.; Molnar, G.L.; Revay, Zs.; Mughabghab, S.F.; Firestone,R.B.; Pronyaev, V.G.; Nichols, A.L.; Moxon, M.C.

    2005-03-03

    The precise value of the thermal capture cross section of238U is uncertain, and evaluated cross sections from various sourcesdiffer by more than their assigned uncertainties. A number of theoriginal publications have been reviewed to assess the discrepant data,corrections were made for more recent standard cross sections andotherconstants, and one new measurement was analyzed. Due to the strongcorrelations in activation measurements, the gamma-ray emissionprobabilities from the beta decay of 239Np were also analyzed. As aresult of the analysis, a value of 2.683 +- 0.012 barns was derived forthe thermal capture cross section of 238U. A new evaluation of thegamma-ray emission probabilities from 239Np decay was alsoundertaken.

  10. Average resonance parameters evaluation for actinides

    Energy Technology Data Exchange (ETDEWEB)

    Porodzinskij, Yu.V.; Sukhovitskij, E.Sh. [Radiation Physics and Chemistry Problems Inst., Minsk-Sosny (Belarus)

    1997-03-01

    New evaluated <{Gamma}{sub n}{sup 0}> and values for {sup 238}U, {sup 237}Np, {sup 243}Cm, {sup 245}Cm, {sup 246}Cm and {sup 241}Am nuclei in the resolved resonance region are presented. The applied method based on the idea that experimental resonance missing results in correlated changes of reduced neutron widths and level spacings distributions is discussed. (author)

  11. Natural radionuclides in urine- and faeces samples; Natuerliche Radionuklide in Urin- und Stuhlproben

    Energy Technology Data Exchange (ETDEWEB)

    Froning, M.; Burow, M.; Ennen, R.; Hoelters, A.; Laumen-Sentis, S.; Zoriy, M. [Forschungszentrum Juelich GmbH (Germany). Geschaeftsbereich Sicherheit und Strahlenschutz

    2016-07-01

    In interpreting of measurement data for incorporation monitoring by excretion samples a clear distinction between the natural intake and the fraction subjected due to occupational exposure should be performed. At the present only a few data about an excretion of primordial elements such as {sup 238}U, {sup 232}Th are available in the literature. In the following study actual data measured in urine and faeces will be presented and discussed.

  12. Radon determination in ground water

    Energy Technology Data Exchange (ETDEWEB)

    Segovia A, N.; Bulbulian G, S

    1991-08-15

    Studies on natural radioactivity in ground water were started in Mexico in San Luis Potosi state followed by samplings from deep wells and springs in the states of Mexico and Michoacan. The samples were analyzed for solubilized and {sup 226} Ra- supported {sup 222} Rn. Some of them were also studied for {sup 234} U/ {sup 238} U activity ratio. In this paper we discuss the activities obtained and their relationship with the geologic characteristics of the studied zones. (Author)

  13. Preliminary survey of outdoor gamma dose rates in Lesvos Island (Greece).

    Science.gov (United States)

    Petalas, Anastasios B; Vogiannis, Efstratios; Nikolopoulos, Dimitrios; Halvadakis, Constantinos P

    2005-01-01

    This study reports the first attempt to record the radioactive background due to gamma radiation in Lesvos Island (Greece). The study reports the results from 335 outdoor total gamma effective dose rate measurements conducted using GPS navigation and a Geiger-Muller detector (Bicron, Micro Sievert) on the whole surface of the island together with a digital map produced by appropriate mapping GIS programme. The study also reports the measurements of outdoor gamma dose rates due to the 238U, 232Th and 40K radionuclides as estimated via in situ gamma-ray spectrometry measurements performed at 26 sites using a 3 x 3 inch NaI (thallium activated) portable detector. The results from the outdoor total gamma effective dose rates range between 0.0023 and 0.28 microSv h(-1). The highest outdoor total gamma effective dose rates (0.013-0.28 microSv h(-1)) were detected in the northeastern part of the island and the intermediate rates (0.066-0.13 microSv h(-1)) in the central region. The outdoor gamma dose rates due to 238U, 232Th and 40K radionuclides range between 1.7 +/- 0.8 and 154 +/- 7 nGy h(-1) with an average of 86 +/- 6 nGy h(-1). The average contribution of each of the examined radionuclides (238U, 232Th and 40K) to the total gamma dose rate was found to be equal to 12 +/- 4% for 238U, 58 +/- 6% for 232Th and 29 +/- 7% for 40K, respectively.

  14. Modelling of reaction cross sections and prompt neutron emission

    Science.gov (United States)

    Hambsch, F.-J.; Tudora, A.; Oberstedt, S.

    2010-10-01

    Accurate nuclear data concerning reaction cross sections and the emission of prompt fission neutrons (i.e. multiplicity and spectra) as well as other fission fragment data are of great importance for reactor physics design, especially for the new Generation IV nuclear energy systems. During the past years for several actinides (238U(n, f) and 237Np(n, f)) both the reaction cross sections and prompt neutron multiplicities and spectra have been calculated within the frame of the EFNUDAT project.

  15. Transportation of the Fission Fragments by the Gas Flow with Aerosol

    CERN Document Server

    Gangrsky, Yu P; Zhemenik, V I; Myshinskii, G V; Penionzhkevich, Yu E; Selesh, O

    2001-01-01

    The experimental set-up for the transportation of the fission fragments by the gaseous flow with aerosols is described. The results of the set-up testing using the {238}U photofission fragments are presented. The obtained parameters (transport efficiency up to 60 % and transport time down to 0.1 s at 1 m distance) allow one to use this set-up in the experiments on the heavy nuclei fission and fragment properties investigation.

  16. Overview of Uranium Isotopic Reference Materials at IRMM

    Science.gov (United States)

    Alonso-Munoz, A.; Richter, S.; Eykens, R.; Aregbe, Y.; Kuehn, H.; Verbruggen, A.

    2007-12-01

    For many applications in the geological sciences, in particular in geochemistry research, isotope ratio measurements play a significant role. For instance, in geochronology isotope abundances of uranium and its daughter products thorium and lead have been used since more than five decades to determine the age of various samples of geological interest. However, in order to validate mass spectrometric measurement procedures and to calibrate detector systems, suitable isotope reference materials are needed. IRMM is a well recognized provider for nuclear isotope reference materials to the nuclear industry and nuclear safeguards authorities, which can also be used for geological applications. This paper gives an overview of isotope reference materials for uranium prepared and certified at IRMM. These materials are synthetic isotope reference materials prepared based on proven methods of purifying and mixing highly enriched oxides. Firstly, a set of 10 mixtures of 233U, 235U and 238U was made in which the 235U/238U ratios were kept at 1:1 and the 233U/235U ratios varied from 1.0 to 10-6 (IRMM-072). This set is ideal for checking the linearity response of detectors used in isotope mass spectrometry. Recently, after the IRMM-072 series was exhausted, it has been replaced by the IRMM-073 and IRMM-074 series. Secondly the double spike IRMM-3636 with a 233U/236U ratio of 1:1 was prepared which allows internal mass fractionation correction for high precision 235U/238U ratio measurements. The 234U abundance of this double spike material is low enough to allow an accurate and precise correction of 234U/238U ratios, even for measurements of close to equilibrium uranium samples.

  17. Assessments of radioactivity concentration of natural radionuclides and radiological hazard indices in sediment samples from the East coast of Tamilnadu, India with statistical approach.

    Science.gov (United States)

    Ravisankar, R; Chandramohan, J; Chandrasekaran, A; Prince Prakash Jebakumar, J; Vijayalakshmi, I; Vijayagopal, P; Venkatraman, B

    2015-08-15

    This paper reports on the distribution of three natural radionuclides (238)U, (232)Th and (40)K in coastal sediments from Pattipulam to Devanampattinam along the East coast of Tamilnadu to establish baseline data for future environmental monitoring. Sediment samples were collected by a Peterson grab samples from 10m water depth parallel to the shore line. Concentration of natural radionuclides were determined using a NaI(Tl) detector based γ-spectrometry. The mean activity concentration is ⩽2.21, 14.29 and 360.23Bqkg(-1) for (238)U, (232)Th and (40)K, respectively. The average activity of (232)Th, (238)U and (40)K is lower when compared to the world average value. Radiological hazard parameters were estimated based on the activity concentrations of (238)U, (232)Th and (40)K to find out any radiation hazard associated with the sediments. The radiological hazard parameters such as radium equivalent activity (Raeq), absorbed gamma dose rates in air (DR), the annual gonadal dose equivalent (AGDE), annual effective dose equivalent (AEDE), external hazard index (Hex) internal hazard index (Hin), activity utilization index (AUI) and excess lifetime cancer (ELCR) associated with the radionuclides were calculated and compared with internationally approved values and the recommended safety limits. Pearson correlation, principal component analysis (PCA) and hierarchical cluster analysis (HCA) have been applied in order to recognize and classify radiological parameters in sediments collected at 22 sites on East coast of Tamilnadu. The values of radiation hazard parameters were comparable to the world averages and below the recommended values. Therefore, coastal sediments do not to pose any significant radiological health risk to the people living in nearby areas along East coast of Tamilnadu. The data obtained in this study will serve as a baseline data in natural radionuclide concentration in sediments along the coastal East coast of Tamilnadu. Copyright © 2015 Elsevier

  18. Activity of Changbaishan Tianchi Volcano Since Late Pleistocene--The Constrain From Geochronology of High Precision U- Series Tims Method

    Institute of Scientific and Technical Information of China (English)

    Wang Fei; Chen Wenji; Zhang Zhonglu; Hu Yutai; Peng Zicheng

    2000-01-01

    11 samples of lava and pumice from the cone of Changbaishan Tianchi Volcano, Jiling, China, were dated by using high precision U - series TIMS method. We conclude that the bottom of the cone formed before 350 ka, the middle part in 70~80 ka, the upper during 20~ 1ka, and the top less than 1ka, and the age based periods of the volcano eruption since Late Pleistocene is given as follows: > 350ka, 70ka, 18 ~ 25ka, 10ka, 4C5ka, 1~0.75ka, which may offer the basis for the study of volcanic disaster in future. In addition, the principle of dating young volcanic rocks by using U - series TIMS method is introduced briefly. Differentiation characteristics of U and Th in different minerals of the volcanic rocks are discussed, and the ability producing isochrons, based on U and Th differentiation, are discussed. In the last part of the paper,the closure of samples to the elements U and Th, which is important for age results, is discussed by using (234U/238U)radioactivity ratio which can be used to monitor if the samples have been weathered or eroded or leached since the time they formed. In this study, all samples have (234U/238U) activity ratios within 1% of secular equilibrium ((234U/238U) radioactivity ratios are unity), indicating no disturbance of the 234U- 238U system. All of these discussions show that the TIMS method is good to date Tianchi volcanics and the results are reliable.

  19. Dating by fission track method: study of neutron dosimetry with natural uranium thin films; Datacao com o metodo dos tracos de fissao: estudo da dosimetria de neutrons com filmes finos de uranio natural

    Energy Technology Data Exchange (ETDEWEB)

    Iunes, P.J.

    1990-06-01

    Fission track dating is described, focalizing the problem of the decay constant for spontaneous fission of {sup 238} U and the use of neutron dosimetry in fission track analysis. Experimental procedures using thin films of natural uranium as neutron dosimeters and its results are presented. The author shows a intercomparison between different thin films and between the dosimetry with thin film and other dosimetries. (M.V.M.). 52 refs, 12 figs, 9 tabs.

  20. Investigation of uranium geochemistry along groundwater flow path in the Continental Intercalaire aquifer (Southern Tunisia).

    Science.gov (United States)

    Dhaoui, Z; Chkir, N; Zouari, K; Ammar, F Hadj; Agoune, A

    2016-06-01

    Environmental tracers ((2)H, (18)O, isotopes of Uranium) and geochemical processes occurring within groundwaters from the Continental Intercalaire (CI) in Southern Tunisia were used to understand the hydrodynamics and the recharge conditions of this aquifer. This study investigates the chemical and isotopic compositions of the CI groundwater. The water types are dominated by Na(+), SO4(2-), Cl(-) throughout most of the basin with a general increase in total dissolved solids from the Saharan Platform margins towards the Chotts region. Large scale groundwater flow paths are toward the Chotts region. The stable isotopes composition of the analyzed groundwater ranges from -8.8 to -6‰ vs V-SMOW for δ(18)O and from -67 to -40‰ vs V-SMOW for δ(2)H. The relatively enriched stable isotopes contents suggest the contribution of the Dahar sandstones outcrops in the current recharge of the CI aquifer in an arid context. However, the most depleted values in heavy isotopes indicate a paleorecharge of the aquifer under wetter conditions revealing a long residence time of groundwaters. The results from water samples using alpha spectrometry method indicate a range in (238)U concentrations and (234)U/(238)U activity ratios (AR) of 0.044-1.285 μg kg(-1) and 1.2 to 8.84 respectively. The geochemistry of uranium isotopes in groundwater is controlled by many factors, essentially, the influence of water rock interactions, the preferential dissolution of (234)U relative to (238)U due to alpha recoil and the mixing processes between different waters with distinct AR as well as (238)U concentrations.

  1. High-/sup 240/Pu sector experiments in ZPPR assembly 4

    Energy Technology Data Exchange (ETDEWEB)

    McFarlane, H F; Beck, C L

    1976-12-01

    The complete high-/sup 240/Pu fuel experiment in ZPPR assembly 4 is reviewed. Results of criticality, enrichment, small-sample perturbation, sodium void, /sup 238/U Doppler, control rod substitution and reaction rate measurements are presented. Comparison of these measured values with calculated results are included where possible. The relationship between the ZPPR high-/sup 240/Pu fuel experiments and the results obtained in previous critical experience is considered.

  2. Evaluation strategies for isotope ratio measurements of single particles by LA-MC-ICPMS.

    Science.gov (United States)

    Kappel, S; Boulyga, S F; Dorta, L; Günther, D; Hattendorf, B; Koffler, D; Laaha, G; Leisch, F; Prohaska, T

    2013-03-01

    Data evaluation is a crucial step when it comes to the determination of accurate and precise isotope ratios computed from transient signals measured by multi-collector-inductively coupled plasma mass spectrometry (MC-ICPMS) coupled to, for example, laser ablation (LA). In the present study, the applicability of different data evaluation strategies (i.e. 'point-by-point', 'integration' and 'linear regression slope' method) for the computation of (235)U/(238)U isotope ratios measured in single particles by LA-MC-ICPMS was investigated. The analyzed uranium oxide particles (i.e. 9073-01-B, CRM U010 and NUSIMEP-7 test samples), having sizes down to the sub-micrometre range, are certified with respect to their (235)U/(238)U isotopic signature, which enabled evaluation of the applied strategies with respect to precision and accuracy. The different strategies were also compared with respect to their expanded uncertainties. Even though the 'point-by-point' method proved to be superior, the other methods are advantageous, as they take weighted signal intensities into account. For the first time, the use of a 'finite mixture model' is presented for the determination of an unknown number of different U isotopic compositions of single particles present on the same planchet. The model uses an algorithm that determines the number of isotopic signatures by attributing individual data points to computed clusters. The (235)U/(238)U isotope ratios are then determined by means of the slopes of linear regressions estimated for each cluster. The model was successfully applied for the accurate determination of different (235)U/(238)U isotope ratios of particles deposited on the NUSIMEP-7 test samples.

  3. Report on scientist exchange program -analysis of uranium series nuclides in rocks and minerals-

    OpenAIRE

    1992-01-01

    This report mainly described the analysis of uranium series nuclidesin samples of rocks and minerials, giving detailed procedures about them. The related analytical methods and techniques included alpha spectrometry for U-238,U-234,Th-232 and Th-230, which employedanion exchange and TBP-tetrachloromethane extraction methods separating uranium and thorium from matrix and electrode position method preparing source disks, gamma spectrometry for Pb-210, Pb-214, Bi-214, Th-234 and Ra-226, oxine-ch...

  4. Assessment of radionuclide and metal contamination in a thorium rich area in Norway.

    Science.gov (United States)

    Popic, Jelena Mrdakovic; Salbu, Brit; Strand, Terje; Skipperud, Lindis

    2011-06-01

    The Fen Central Complex in southern Norway, a geologically well investigated area of magmatic carbonatite rocks, is assumed to be among the world largest natural reservoirs of thorium ((232)Th). These rocks, also rich in iron (Fe), niobium (Nb), uranium ((238)U) and rare earth elements (REE), were mined in several past centuries. Waste locations, giving rise to enhanced levels of both radionuclides and metals, are now situated in the area. Estimation of radionuclide and metal contamination of the environment and radiological risk assessment were done in this study. The average outdoor gamma dose rate measured in Fen, 2.71 μGy h(-1), was significantly higher than the world average dose rate of 0.059 μGy h(-1). The annual exposure dose from terrestrial gamma radiation, related to outdoor occupancy, was in the range 0.18-9.82 mSv. The total activity concentrations of (232)Th and (238)U in soil ranged from 69 to 6581 and from 49 to 130 Bq kg(-1), respectively. Enhanced concentrations were also identified for metals, arsenic (As), lead (Pb), chromium (Cr) and zinc (Zn), in the vicinity of former mining sites. Both radionuclide and heavy metal concentrations suggested leaching, mobilization and distribution from rocks into the soil. Correlation analysis indicated different origins for (232)Th and (238)U, but same or similar for (232)Th and metals As, Cr, Zn, nickel (Ni) and cadmium (Cd). The results from in situ size fractionation of water demonstrated radionuclides predominately present as colloids and low molecular mass (LMM) species, being potentially mobile and available for uptake in aquatic organisms of Norsjø Lake. Transfer factors, calculated for different plant species, showed the highest radionuclide accumulation in mosses and lichens. Uptake in trees was, as expected, lower. Relationship analysis of (232)Th and (238)U concentrations in moss and soil samples showed a significant positive linear correlation.

  5. Single-particle isomeric states in 121Pd and 117Ru

    CERN Document Server

    Lalkovski, S; Bacelar, A M Denis; Gorska, M; Pietri, S; Podolyak, Zs; Bednarczyk, P; Caceres, L; Casarejos, E; Cullen, I J; Doornenbal, P; Farrelly, G F; Garnsworthy, A B; Geissel, H; Gelletly, W; Gerl, J; Grcebosz, J; Hinke, C; Ilie, G; Jaworski, G; Kisyov, S; Kojouharov, I; Kurz, N; Myalski, S; Palacz, M; Prokopowicz, W; Regan, P H; Schaffner, H; Steer, S; Tashenov, S; Walker, P M; Wollersheim, H J; Zhekova, M

    2011-01-01

    Neutron-rich nuclei were populated in a relativistic fission of 238U. Gamma-rays with energies of 135 keV and 184 keV were associated with two isomeric states in 121Pd and 117Ru. Half-lives of 0.63(5) microseconds and 2.0(3) micrisecondss were deduced and the isomeric states were interpreted in terms of deformed single-particle states.

  6. Fukushima plutonium effect and blow-up regimes in neutron-multiplying media

    CERN Document Server

    Rusov, V D; Vaschenko, V M; Linnik, E P; Zelentsova, T N; Beglaryan, M E; Chernegenko, S A; Kosenko, S I; Molchinikolov, P A; Smolyar, V P; Grechan, E V

    2012-01-01

    It is shown that the capture and fission cross-sections of 238U and 239Pu increase with temperature within 1000-3000K range, in contrast to those of 235U, that under certain conditions may lead to the so-called blow-up modes, stimulating the anomalous neutron flux and nuclear fuel temperature growth. Some features of the blow-up regimes in neutron-multiplying media are discussed.

  7. Excess /sup 129/Xe in terrestrial samples: A non-primordial hypothesis

    Energy Technology Data Exchange (ETDEWEB)

    Caffee, M.W.; Hudson, G.B.

    1987-03-01

    Excesses of /sup 129/Xe relative to the isotopic composition in air are observed in some terrestrial samples. Traditionally these /sup 129/Xe excesses have been thought to be related to /sup 129/I that was present in abundance in the early solar system. We propose an alternative hypothesis to explain terrestrial /sup 129/Xe excesses based on the production of /sup 129/I from the spontaneous fission of /sup 238/U.

  8. Natural radioactivity and radiological hazard assessment of Egyptian oil ashes.

    Science.gov (United States)

    Mohammed, Hesham; Sadeek, Sadeek; Mahmoud, Abu Rehab; Diab, Hanan; Zaky, Doaa

    2016-08-01

    Oil fly and boiler ash samples were collected from the four major Egyptian power plants in order to determine their natural radioactivity. Secular equilibrium between (238)U and (232)Th and their decay products is significantly disturbed in oil ash samples. The (226)Ra/(238)U ratios were between 440 and 1993 with an average value of 801, indicating that the concentrations of daughters (226)Ra were very high compared to the parent (238)U in the oil ash samples. While, the average ratios for (210)Pb/(226)Ra in most samples were 1.19 ± 0.05, indicating a secular equilibrium in the (226)Ra-(210)Pb sub series. The natural radioactivity due to (238)U and (232)Th was found to be negligible. While the activity concentrations of (226)Ra ranged from 3205 to 12,320 Bq kg(-1) with an average value of 9284 Bq kg(-1), (210)Pb ranged from 5960 to 13,930 Bq kg(-1) with an average value of 11,513 Bq kg(-1). The results are compared with the reported data from other countries. The average value of radium equivalent activity was 9308 ± 2729 Bq kg(-1), while the external and internal hazard indexes were found to be 25 ± 7 and 50 ± 15, respectively. All the studied radiological parameters were higher than the recommended limit by the IAEA in all ash samples.

  9. Estimates of micro-, nano-, and picoplankton contributions to particle export in the northeast Pacific

    OpenAIRE

    Mackinson, B. L.; S. B. Moran; M. W. Lomas; Stewart, G M; R. P. Kelly

    2014-01-01

    The contributions of micro-, nano-, and picoplankton to particle export were estimated from measurements of size-fractionated particulate 234Th, organic carbon, and phytoplankton indicator pigments obtained during five cruises between 2010 and 2012 along Line P in the subarctic northeast Pacific Ocean. Sinking fluxes of particulate organic carbon (POC) and indicator pigments were calculated from 234Th–238U disequilibria and, during two cruises, measured by s...

  10. Estimates of micro-, nano-, and picoplankton contributions to particle export in the northeast Pacific

    OpenAIRE

    Mackinson, B. L.; S. B. Moran; M. W. Lomas; Stewart, G M; R. P. Kelly

    2015-01-01

    The contributions of micro-, nano-, and picoplankton to particle export were estimated from measurements of size-fractionated particulate 234Th, organic carbon, and phytoplankton indicator pigments obtained during five cruises between 2010 and 2012 along Line P in the subarctic northeast Pacific Ocean. Sinking fluxes of particulate organic carbon (POC) and indicator pigments were calculated from 234Th–238U disequilibria and, during two cruises, measured by a sediment trap at...

  11. Assessment of natural radioactivity levels in rocks and their relationships with the geological structure of Johor state, Malaysia.

    Science.gov (United States)

    Alnour, I A; Wagiran, H; Ibrahim, N; Hamzah, S; Elias, M S; Laili, Z; Omar, M

    2014-01-01

    The distribution of natural radionuclides ((238)U, (232)Th and (40)K) and their radiological hazard effect in rocks collected from the state of Johor, Malaysia were determined by gamma spectroscopy using a high-purity germanium detector. The highest values of (238)U, (232)Th and (40)K activity concentrations (67±6, 85±7 and 722±18 Bg kg(-1), respectively) were observed in the granite rock. The lowest concentrations of (238)U and (232)Th (2±0.1 Bq kg(-1) for (238)U and 2±0.1 Bq kg(-1) for (232)Th) were observed in gabbro rock. The lowest concentration of (40)K (45±2 Bq kg(-1)) was detected in sandstone. The radium equivalent activity concentrations for all rock samples investigated were lower than the internationally accepted value of 370 Bq kg(-1). The highest value of radium equivalent in the present study (239±17 Bq kg(-1)) was recorded in the area of granite belonging to an acid intrusive rock geological structure. The absorbed dose rate was found to range from 4 to 112 nGy h(-1). The effective dose ranged from 5 to 138 μSv h(-1). The internal and external hazard index values were given in results lower than unity. The purpose of this study is to provide information related to radioactivity background levels and the effects of radiation on residents in the study area under investigation. Moreover, the relationships between the radioactivity levels in the rocks within the geological structure of the studied area are discussed.

  12. Measurement of the Ratio of High Energy Neutron in the Pulse Nuclear Reactor

    Institute of Scientific and Technical Information of China (English)

    MAO; Guo-shu; DING; You-qian; YANG; Lei; MA; Peng; YU; Zhen-hua

    2012-01-01

    <正>In the production of radioisotopes and neutron activation analysis, the fast neutron densities are very important to estimate the yields of the radioisotopes. In order to determine the fast neutron flux ratio, different foils are used to measure the thermal neutron flux and the fast neutron flux. In this paper 238U was used as only a monitor to measure the ratio of high energy neutron (>6 MeV). By measuring the

  13. Zircon U-Pb Age Determination of Volcanic Eruptions in Lutao and Lanyu in the Northern Luzon Magmatic Arc

    Directory of Open Access Journals (Sweden)

    Wen-Yu Shao

    2014-01-01

    Full Text Available This paper reports for the first time zircon U-Pb ages of volcanic rocks and sands from Lutao and Lanyu, two islets off SE Taiwan in the north Luzon arc. The samples include (1 seven andesites from four volcanic units and three river/beach sands from Lutao and (2 five basaltic andesites from four volcanic units and two river/beach sands from Lanyu. The Lutao andesites contain abundant magmatic zircons, aging from ~1.54 to ~1.24 Ma for individual sample, which yielded an overall mean 206Pb/238U age of 1.31 ±± 0.03 Ma (n = 190, MSWD = 2.6. This is slightly older than, or broadly coincident with, a mean 206Pb/238U age of 1.23 ±± 0.03 Ma (n = 103, MSWD = 1.9 given by detrital zircons from the three sands. The Lanyu volcanics appear to have less abundant magmatic zircons, aging from ~2.72 to ~2.35 Ma for individual sample, which yielded an overall mean 206Pb/238U age of 2.61 ±± 0.13 Ma (n = 11, MSWD = 1.8. This accords with a mean 206Pb/238U age of 2.69 ±± 0.11 Ma (n = 34, MSWD = 4.7 obtained by detrital zircons from the two sands. The age data suggest that in Lutao and Lanyu the major volcanic eruptions occurred at ~1.3 and ~2.6 Ma, respectively. Moreover, volcanic samples from both islets contain various amounts of older inherited zircons, ~11% in Lutao and up to ~82% in Lanyu, which together with detrital zircons from the sands show main age peaks at ~150 Ma and ~1.9 and ~2.5 Ga, consistent with the notion for a _ continental crust involved in the genesis of the northern Luzon magmatic arc.

  14. Natural radionuclides in mineral fertilizers and farmland

    Directory of Open Access Journals (Sweden)

    Mitrović Branislava M.

    2013-01-01

    Full Text Available Contemporary agriculture production is based on use of mineral fertilizers, which however can have high activity of natural radionuclides and so cause the appearance of technologically elevated radioactivity. In order to determine the influence of mineral fertilizers application in arable land, there was used gamma spectrometric method for defining the activity of natural radionuclides (40 K, 238U, 226Ra in imported mineral fertilizers as well as in arable and fallow land in the area of suburban municipalities of Belgrade. The obtained results have shown that in the tested mineral fertilizers the measured activity of 40K ranged from 70 to 4590 Bq/kg, 238U from 18 to 1400 Bq/kg and 226Ra from 15 to 999Bq/kg. Average activities of natural radionuclides in arable land are: 626 Bq/kg for 40K, 54 Bq/kg for 238U, 55 Bq/kg for 226Ra and 55Bq/kg for 232Th, and in fallow land 596 Bq/kg for 40K, 54 Bq/kg for 238U, 54 Bq/kg for 226Ra and 53 Bq/kg for 232Th. Average values of radium radioactivity equivalent (175 Bq/kg and index of radiation risk (0,48, point out that in the tested areas there is no significant radiation risk for inhabitants due to terrestrial exposure. This investigation has also shown that current use of mineral fertilizers has not caused the increase of natural radioactivity in the tested arable land. [Projekat Ministarstva nauke Republike Srbije, br. TR 31003

  15. Episodic Holocene eruption of the Salton Buttes rhyolites, California, from paleomagnetic, U-Th, and Ar/Ar dating

    Science.gov (United States)

    Wright, Heather M.; Vazquez, Jorge A.; Champion, Duane E.; Calvert, Andrew T.; Mangan, Margaret T.; Stelten, Mark; Cooper, Kari M.; Herzig, Charles; Schriener, Alexander

    2015-04-01

    In the Salton Trough, CA, five rhyolite domes form the Salton Buttes: Mullet Island, Obsidian Butte, Rock Hill, North and South Red Hill, from oldest to youngest. Results presented here include 40Ar/39Ar anorthoclase ages, 238U-230Th zircon crystallization ages, and comparison of remanent paleomagnetic directions with the secular variation curve, which indicate that all domes are Holocene. 238U-230Th zircon crystallization ages are more precise than but within uncertainty of 40Ar/39Ar anorthoclase ages, suggesting that zircon crystallization proceeded until shortly before eruption in all cases except one. Remanent paleomagnetic directions require three eruption periods: (1) Mullet Island, (2) Obsidian Butte, and (3) Rock Hill, North Red Hill, and South Red Hill. Borehole cuttings logs document up to two shallow tephra layers. North and South Red Hills likely erupted within 100 years of each other, with a combined 238U-230Th zircon isochron age of: 2.83 ± 0.60 ka (2 sigma); paleomagnetic evidence suggests this age predates eruption by hundreds of years (1800 cal BP). Rock Hill erupted closely in time to these eruptions. The Obsidian Butte 238U-230Th isochron age (2.86 ± 0.96 ka) is nearly identical to the combined Red Hill age, but its Virtual Geomagnetic Pole position suggests a slightly older age. The age of aphyric Mullet Island dome is the least well constrained: zircon crystals are resorbed and the paleomagnetic direction is most distinct; possible Mullet Island ages include ca. 2300, 5900, 6900, and 7700 cal BP. Our results constrain the duration of Salton Buttes volcanism to between ca. 5900 and 500 years.

  16. Evaluation of Differences in Response of DOD Portable Instruments and Solid-State Detectors used by MEXT for Measurement of External Radiations with Attention to the Cosmic Radiation Component

    Science.gov (United States)

    2014-03-01

    reporting burden for this collection of information is estimated to average 1 hour per response, including the time for reviewing instructions, searching...in reported results that is operator-induced. Third, an under-response of MEXT solid- state scintillators , such as thallium-activated sodium iodide...naturally-occurring radioactive materials in the environment are 232Th (and radioactive decay products), 238U (and radioactive decay products), and 40K

  17. Evaluation of metal and radionuclide data from neutron activation and acid-digestion-based spectrometry analyses of background soils: Significance in environmental restoration

    Energy Technology Data Exchange (ETDEWEB)

    Lee, S.Y.; Watkins, D.R.; Jackson, B.L.; Schmoyer, R.L. [Oak Ridge National Lab., TN (United States); Lietzke, D.A.; Burgoa, B.B.; Branson, J.T.; Ammons, J.T. [Univ. of Tennessee, Knoxville, TN (United States)

    1995-12-31

    A faster, more cost-effective, and higher-quality data acquisition procedure for natural background-level metals and radionuclides in soils is needed for remedial investigations of contaminated sites. In this project, a total of 120 soil samples were collected from uncontaminated areas on and near the Oak Ridge Reservation. The samples were taken at three different depths and from three different geologic groups to establish background concentrations of metals and radionuclides. The objective of this presentation is to discuss the advantages and disadvantages of neutron activation analysis (NAA) compared with those of acid-digestion-based spectrometry (ADS) methods; the advantages and disadvantages were evaluated from Al, Sb, As, Cr, Co, Fe, Mg, Mn, Hg, K, Ag, {sup 232}Th, {sup 235}U, {sup 238}U, V, and Zn data. The ADS methods used for this project were inductively coupled plasma (ICP), ICP-mass spectrometry (ICP-MS), and alpha spectrometry. The scatter plots showed that the NAA results for As, Co, Fe, Mn, {sup 232}Th, and {sup 238}U are reasonably correlated with the results from the other analytical methods. Compared to NAA, however, the ADS methods underestimated Al, Cr, Mg, K, V, and Zn. The skew distributions were caused by incomplete dissolution of the analytes during acid digestion of the soil samples. Because of the high detection limits of the spectrometric methods, the NAA results and the ADS results for some elements, including Sb, Hg, and Ag, did not show a definite relationship. The NAA results were highly correlated with the alpha spectrometry results for {sup 232}Th and {sup 238}U but poorly correlated for {sup 235}U, probably because of a larger counting error associated with the lower activity of the isotope. The NAA methods, including the delayed neutron counting method, were far superior techniques for quantifying background levels of radionuclides ({sup 232}Th, {sup 235}U, and {sup 238}U) and metals (Al, Cr, Mg, K, V, and Zn) in soils.

  18. Uranium and plutonium in anoxic marine sediments of the Santiago River mouth (Eastern Pacific, Mexico).

    Science.gov (United States)

    Almazán-Torres, María Guadalupe; Ordóñez-Regil, Eduardo; Ruiz-Fernández, Ana Carolina

    2016-11-01

    The uranium (U) and plutonium (Pu) content with depth in a sediment core collected in the continental shelf off the mouth of the Santiago River in the Mexican Pacific was studied to evaluate the contamination effects of the effluent of the Santiago-Lerma River as it moves into the sea. The large mass of terrestrial detritus delivered by the river influences the physicochemical and geochemical processes in the seafloor. Abnormal concentrations of U and Pu in sediments were examined as indicative of the effects of anoxic conditions. One of the indicators of pollution of seawater is the bacterial activity of the shallow seabed layer; and among the prevailing bacteria, the magnetotactic ones induce the formation of euhedral and framboidal shapes (pyrite). These pyrite entities are by-products of anoxic environments loaded with decomposing detrital material and are very abundant in the surface layers of the sediment core analyzed. The pyrite formation is the result of a biochemical reaction between iron and organic sulphur reduced by bacteria, and the pyrite entities precipitate to the seafloor. In the same upper zone of the profile, (238)U is readily immobilized, while (234)U is oxidized and dissolved in seawater by the effect of hot atom chemistry. This may cause the activity ratio (AR) (234)U/(238)U disequilibrium (near 0.41). Furthermore, in the shallow layer of the sediment core, an abnormally high concentration of (239+240)Pu was detected. In this upper layer, the activity concentrations found were 3.19 Bq kg(-1) for (238)U, 1.32 kg(-1) for (234)U and 2.78 Bq kg(-1) for (239+240)Pu. In the lower fractions of the sediment core, normal values of AR (234)U/(238)U (≈1) were found, with traces of (239+240)Pu.

  19. Estimates of micro-, nano-, and picoplankton contributions to particle export in the northeast Pacific

    OpenAIRE

    B. L. Mackinson; Moran, S. B.; M. W. Lomas; Stewart, G. M.; Kelly, R.P.

    2014-01-01

    The contributions of micro-, nano-, and picoplankton to particle export were estimated from measurements of size-fractionated particulate 234Th, organic carbon, and phytoplankton indicator pigments obtained during five cruises between 2010 and 2012 along Line P in the subarctic northeast Pacific Ocean. Sinking fluxes of particulate organic carbon (POC) and indicator pigments were calculated from 234Th–238U disequilibria and, during two cruises, measured by s...

  20. Estimates of micro-, nano-, and picoplankton contributions to particle export in the northeast Pacific

    OpenAIRE

    B. L. Mackinson; Moran, S. B.; M. W. Lomas; Stewart, G. M.; Kelly, R.P.

    2015-01-01

    The contributions of micro-, nano-, and picoplankton to particle export were estimated from measurements of size-fractionated particulate 234Th, organic carbon, and phytoplankton indicator pigments obtained during five cruises between 2010 and 2012 along Line P in the subarctic northeast Pacific Ocean. Sinking fluxes of particulate organic carbon (POC) and indicator pigments were calculated from 234Th–238U disequilibria and, during two cruises, measured by a sediment trap at...

  1. Average resonance parameters evaluation for actinides

    Energy Technology Data Exchange (ETDEWEB)

    Porodzinskij, Yu.V.; Sukhovitskij, E.Sh. [Radiation Physics and Chemistry Problems Inst., Minsk-Sosny (Belarus)

    1997-03-01

    New evaluated <{Gamma}{sub n}{sup 0}> and values for {sup 238}U, {sup 237}Np, {sup 243}Cm, {sup 245}Cm, {sup 246}Cm and {sup 241}Am nuclei in the resolved resonance region are presented. The applied method based on the idea that experimental resonance missing results in correlated changes of reduced neutron widths and level spacings distributions is discussed. (author)

  2. Preliminary concepts: coordinated safeguards for materials management in a thorium--uranium fuel reprocessing plant

    Energy Technology Data Exchange (ETDEWEB)

    Hakkila, E.A.; Barnes, J.W.; Dayem, H.A.; Dietz, R.J.; Shipley, J.P.

    1978-10-01

    This report addresses preliminary concepts for coordinated safeguards materials management in a typical generic thorium--uranium-fueled light-water reactor (LWR) fuels reprocessing plant. The reference facility is designed to recover thorium and uranium from first-generation (denatured /sup 235/U) startup fuels, first-recycle and equilibrium (denatured /sup 233/U) thorium--uranium LWR fuels, and to recover the plutonium generated in the /sup 238/U denaturant as well. 12 figures, 3 tables.

  3. Study of pollution in the El Jadida-Safi Atlantic coastal zone (Morocco) by using PIXE and SSNTD methods

    OpenAIRE

    2008-01-01

    International audience; In this work PIXE experiments were performed for measuring heavy and light elements (ranging from aluminium to lead) concentrations inside various polluted and unpolluted soils as well as liquid samples collected from different phosphate factory sewers in the El Jadida-Safi Atlantic coastal region (Morocco). In addition, uranium (238U) and thorium (232Th) contents were evaluated in the same samples studied by using CR-39 and LR-115 type II solid state nuclear track det...

  4. Compensation effects in hadron calorimeters

    Energy Technology Data Exchange (ETDEWEB)

    Gabriel, T.A.; Bishop, B.L.; Brau, J.; Di Ciaccio, A.; Goodman, M.; Wilson, R.

    1984-01-01

    The pros and cons of utilizing a fissionable material such as /sup 238/U to compensate for the nuclear binding energy losses in a hadron calorimeter are discussed. Fissionable material can return some lost energy to the particle cascade in terms of low-energy neutrons and gamma rays, but electromagnetic sampling inefficiencies (often called transition effects) and the detection medium which tries to convert this energy to a useable signal are just as important. 12 references.

  5. Opening of the Tethys in southwest China and its significance to the breakup of East Gondwanaland in late Paleozoic: Evidence from SHRIMP U-Pb zircon analyses for the Garzê ophiolite block

    Institute of Scientific and Technical Information of China (English)

    YAN Quanren; WANG Jianguo; ZHANG Dehui; ZHAO Jian; WANG Zongqi; LIU Shuwen; LI Qiugen; ZHANG Hongyuan; WANG Tao; LIU Dunyi; SHI Yuruo; JIAN Ping

    2005-01-01

    SHRIMP U-Pb zircon analyses for a gabbro sample from the Garzê ophiolite block yielded a mean 206Pb/238U age of 292±4 Ma, which indicated that the spreading time of the Garzê-Litang Tethys was most likely at the earliest Permian. Combined with previous studies, we suggest that the opening of the Tethys in southwest China was derived from breakup of the East Gondwanaland in the late Paleozoic.

  6. Evaluation of new geological reference materials for uranium-series measurements: Chinese Geological Standard Glasses (CGSG) and macusanite obsidian.

    Science.gov (United States)

    Denton, J S; Murrell, M T; Goldstein, S J; Nunn, A J; Amato, R S; Hinrichs, K A

    2013-10-15

    Recent advances in high-resolution, rapid, in situ microanalytical techniques present numerous opportunities for the analytical community, provided accurately characterized reference materials are available. Here, we present multicollector thermal ionization mass spectrometry (MC-TIMS) and multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) uranium and thorium concentration and isotopic data obtained by isotope dilution for a suite of newly available Chinese Geological Standard Glasses (CGSG) designed for microanalysis. These glasses exhibit a range of compositions including basalt, syenite, andesite, and a soil. Uranium concentrations for these glasses range from ∼2 to 14 μg g(-1), Th/U weight ratios range from ∼4 to 6, (234)U/(238)U activity ratios range from 0.93 to 1.02, and (230)Th/(238)U activity ratios range from 0.98 to 1.12. Uranium and thorium concentration and isotopic data are also presented for a rhyolitic obsidian from Macusani, SE Peru (macusanite). This glass can also be used as a rhyolitic reference material, has a very low Th/U weight ratio (around 0.077), and is approximately in (238)U-(234)U-(230)Th secular equilibrium. The U-Th concentration data agree with but are significantly more precise than those previously measured. U-Th concentration and isotopic data agree within estimated errors for the two measurement techniques, providing validation of the two methods. The large (238)U-(234)U-(230)Th disequilibria for some of the glasses, along with the wide range in their chemical compositions and Th/U ratios should provide useful reference points for the U-series analytical community.

  7. Study on transfers of uranium, thorium and decay products from grain, water and soil to chicken meat and egg contents.

    Science.gov (United States)

    Jeambrun, M; Pourcelot, L; Mercat, C; Boulet, B; Loyen, J; Cagnat, X; Gauthier-Lafaye, F

    2012-08-01

    Activity concentrations of the uranium and thorium series radionuclides were determined in chicken meat and eggs as well as in soil, water and other dietary intakes of poultry at five sites of the French territory. These data allow the calculation of transfer coefficients which enrich the database given by the technical report series no. 472 of the IAEA. In egg contents, the highest activity concentrations (in mBq kg(-1) fresh weight) are for (226)Ra, ranging between 136 and 190 and are much lower for uranium (between 0.51 and 1.30 for (238)U). In chicken meat, (238)U activity concentration is higher than in egg contents and ranges between 1.7 and 9.7. Concerning (232)Th, its activity concentration is lower than uranium and ranges between 0.5 and 4.9. Daily ingested activity concentration by the animals was assessed taking into account the activity concentrations measured in the grains, in the soil and in the drinking water. The activity concentration in grains and the daily intakes allow the calculation of concentration ratios and transfer coefficients for chicken meat and egg contents. In chicken meat the transfer coefficients (d kg(-1)) range between 0.0018 and 0.0073 for (238)U and between 0.0008 and 0.0028 for (232)Th. In egg contents they range from 0.00018 to 0.0018 for (238)U and are much higher for radium isotopes (0.10-0.23 for (226)Ra and 0.07-0.11 for (228)Ra).

  8. Results of the radiological survey at the former Chapman Valve Manufacturing Company, Indian Orchard, Massachusetts (CIO001)

    Energy Technology Data Exchange (ETDEWEB)

    Foley, R.D.; Uziel, M.S.

    1992-07-01

    Radiological survey was conducted at Building 23 (Department No. 40) at the former Chapman Valve Manufacturing Company, Indian Orchard, Massachusetts. The survey was performed in August 1991. The purpose of the survey was to determine whether the property was contaminated with radioactive residues, principally {sup 238}U, as a result of work done for the Atomic Energy Commission (AEC) during the 1940s. The survey included a gamma scan, a beta-gamma scan, and measurement of alpha activity; measurement of direct and removable alpha and beta-gamma levels; and the collection of soil, dust, debris, and smear samples for radionuclide analyses. Survey emphasis was on interior floors, walls, and overhead beams. Radionuclide analysis of soil, dust, and debris, and analysis of smear samples indicate that residual {sup 238}U attributable to former AEC-supported operations is present at this site. Elevated levels of radioactivity were particularly evident on the floors and walls in the western part of the central area of the building (grid blocks Al through A6). Concentrations of {sup 238}U in dust samples collected from overhead beams exceeded DOE guidelines in grid blocks Al through A14 and remained elevated in grid blocks A15 through A19. Dust on a movable overhead crane in grid block A23 was well above the guideline, probably because the crane had at some time been located further west. Some contamination was evident in grid blocks B1 through B5, but clutter and debris in this area prevented a thorough survey.

  9. Method for (236)U Determination in Seawater Using Flow Injection Extraction Chromatography and Accelerator Mass Spectrometry.

    Science.gov (United States)

    Qiao, Jixin; Hou, Xiaolin; Steier, Peter; Nielsen, Sven; Golser, Robin

    2015-07-21

    An automated analytical method implemented in a flow injection (FI) system was developed for rapid determination of (236)U in 10 L seawater samples. (238)U was used as a chemical yield tracer for the whole procedure, in which extraction chromatography (UTEVA) was exploited to purify uranium, after an effective iron hydroxide coprecipitation. Accelerator mass spectrometry (AMS) was applied for quantifying the (236)U/(238)U ratio, and inductively coupled plasma mass spectrometry (ICPMS) was used to determine the absolute concentration of (238)U; thus, the concentration of (236)U can be calculated. The key experimental parameters affecting the analytical effectiveness were investigated and optimized in order to achieve high chemical yields and simple and rapid analysis as well as low procedure background. Besides, the operational conditions for the target preparation prior to the AMS measurement were optimized, on the basis of studying the coprecipitation behavior of uranium with iron hydroxide. The analytical results indicate that the developed method is simple and robust, providing satisfactory chemical yields (80-100%) and high analysis speed (4 h/sample), which could be an appealing alternative to conventional manual methods for (236)U determination in its tracer application.

  10. U-Pb dating of zircon from the Central Zone of the East Kunlun Orogen and its implications for tectonic evolution

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    LA-ICP-MS and SHRIMP U-Pb dating of zircons from orthogneisses and amphibolite from the Central Zone of the Kunlun Orogen is reported in this paper. One orthogneiss sample has metamorphic zircons yielding weighted average 206Pb/238U age of 517.0 +5.0/-6.0 Ma, and the other orthogneiss sample con- tains zircons with inherited magmatic cores giving three population 207Pb/206Pb ages of 955 Ma, 895 Ma and 657 Ma for the magmatic protolith, and metamorphic recrystallized rims with peak 206Pb/238U ages of 559 +12/?17 Ma and 516 ± 13 Ma. The amphibolite yielded three populations of weighted average 206Pb/238U age of 482.0 +10/?8.0 Ma, 516.2 ± 5.8 Ma and 549 ± 10 Ma for the metamorphic zircons. These dating results recorded the tectonothermal events that occurred in the early Paleozoic and the Pre- cambrian time. The records of the Cambrian magmatic-metamorphic event in the Qinling Orogen, the Altyn Tagh belt, north margin of the Qaidam Block and the Kunlun Orogen suggest that continental assembly probably occurred in the early evolutionary history of the Proto-Tethys.

  11. Uranium isotopes in groundwater from the continental intercalaire aquifer in Algerian Tunisian Sahara (Northern Africa).

    Science.gov (United States)

    Chkir, N; Guendouz, A; Zouari, K; Hadj Ammar, F; Moulla, A S

    2009-08-01

    The disequilibrium between (234)U and (238)U is commonly used as a tracer of groundwater flow. This paper aims to identify uranium contents and uranium isotopic disequilibria variation in groundwater sampled from deep Continental Intercalaire aquifer (southern Algeria and Tunisia). Large variations in both U contents (0.006-3.39ppb) and (234)U/(238)U activity ratios (0.4-15.38) are observed. We conduct a first assessment in order to verify whether the results of our investigation support and complete previous hydrogeological and isotopic studies. The dissolved U content and (234)U/(238)U activity ratio data were plotted on a two-dimensional diagram that was successfully utilized on sharing the CI aquifer into different compartments submitted to different oxidising/reducing conditions and leads also to distinguished two preferential flow paths in the Nefzaoua/Chott Fejej discharge area. Uranium isotopes disequilibrium indicate that ranium chemistry is mainly controlled by water-rock interaction enhanced by long residence time recognised for this aquifer.

  12. Radon in soil gas in Kosovo.

    Science.gov (United States)

    Kikaj, Dafina; Jeran, Zvonka; Bahtijari, Meleq; Stegnar, Peter

    2016-11-01

    An assessment of the radiological situation due to exposure to radon and gamma emitting radionuclides was conducted in southern Kosovo. This study deals with sources of radon in soil gas. A long-term study of radon concentrations in the soil gas was carried out using the SSNTDs (CR-39) at 21 different locations in the Sharr-Korabi zone. The detectors were exposed for an extended period of time, including at least three seasonal periods in a year and the sampling locations were chosen with respect to lithology. In order to determine the concentration of the natural radioactive elements (238)U and (226)Ra, as a precursor of (222)Rn, soil samples were collected from each measuring point from a depth of 0.8 m, and measured by gamma spectrometry. The levels (Bq kg(-1)) of naturally occurring radionuclides and levels (kBq m(-3)) of radon in soil gas obtained at a depth 0.8 m of soil were: 21-53 for (226)Ra, 22-160 for (238)U and 0.295-32 for (222)Rn. With respect to lithology, the highest value for (238)U and (226)Ra were found in limestone and the highest value for (222)Rn was found in metamorphic rocks. In addition, the results showed seasonal variations of the measured soil gas radon concentrations with maximum concentration in the spring months. Copyright © 2016 Elsevier Ltd. All rights reserved.

  13. An Ultra-Low Background PMT for Liquid Xenon Detectors

    CERN Document Server

    Akerib, D S; Bernard, E; Bernstein, A; Bradley, A; Byram, D; Cahn, S B; Carmona-Benitez, M C; Carr, D; Chapman, J J; Chan, Y-D; Clark, K; Coffey, T; deViveiros, L; Dragowsky, M; Druszkiewicz, E; Edwards, B; Faham, C H; Fiorucci, S; Gaitskell, R J; Gibson, K R; Hall, C; Hanhardt, M; Holbrook, B; Ihm, M; Jacobsen, R G; Kastens, L; Kazkaz, K; Larsen, N; Lee, C; Lesko, K; Lindote, A; Lopes, M I; Lyashenko, A; Malling, D C; Mannino, R; McKinsey, D; Mei, D; Mock, J; Morii, M; Nelson, H; Neves, F; Nikkel, J A; Pangilinan, M; Pech, K; Phelps, P; Shutt, T; Silva, C; Skulski, W; Solovov, V N; Sorensen, P; Spaans, J; Stiegler, T; Sweany, M; Szydagis, M; Taylor, D; Thomson, J; Tripathi, M; Uvarov, S; Verbus, J R; Walsh, N; Webb, R; White, J T; Wlasenko, M; Wolfs, F L H; Woods, M; Zhang, C

    2012-01-01

    Results are presented from radioactivity screening of two models of photomultiplier tubes designed for use in current and future liquid xenon experiments. The Hamamatsu 5.6 cm diameter R8778 PMT, used in the LUX dark matter experiment, has yielded a positive detection of four common radioactive isotopes: 238U, 232Th, 40K, and 60Co. Screening of LUX materials has rendered backgrounds from other detector materials subdominant to the R8778 contribution. A prototype Hamamatsu 7.6 cm diameter R11410 MOD PMT has also been screened, with benchmark isotope counts measured at <0.4 238 U / <0.3 232 Th / <8.3 40 K / 2.0+-0.2 60 Co mBq/PMT. This represents a large reduction, equal to a change of \\times 1/24 238U / \\times 1/9 232Th / \\times 1/8 40K per PMT, between R8778 and R11410 MOD, concurrent with a doubling of the photocathode surface area (4.5 cm to 6.4 cm diameter). 60Co measurements are comparable between the PMTs, but can be significantly reduced in future R11410 MOD units through further material selec...

  14. Alpha and gamma spectrometry for natural radioactive nuclides around uranium mines and nuclear power plants

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez, A.M.; Tome, F.V.; Bejarano, J.D.; Aparicio, A.G. (Universidad de Extremadura, Badajoz (Spain). Dept. de Fisica)

    1992-01-01

    Concentration of uranium and [sup 234]U/[sup 238]U and [sup 235]U/[sup 238]U activity ratios were studied in water samples taken in the neighbourhood of two uranium mines ('El Lobo' and 'El Pedregal', Badajoz, Spain), and around two nuclear power plants and their cooling reservoirs (the Central Nuclear de Almaraz, which is working today, and the Central Nuclear de Valdecaballeros, which is in the construction phase), using alpha spectrometry with semiconductor detectors. The Valdecaballeros data were taken to check for comparison with those of the Central Nuclear de Almaraz and with future values after the start of operation. Measurements were also made of all soluble gamma emitting nuclides using a shielded coaxial high purity germanium detector. The data suggest that the mechanisms responsible for the changes in the concentrations and in the [sup 234]U/[sup 238]U activity ratios in surface waters are principally dilution and leaching. (author).

  15. The Surrogate Method: Past, Present and Future

    Energy Technology Data Exchange (ETDEWEB)

    Lesher, S R; Bernstein, L A; Burke, J T; Lyles, B F; Clark, R M; Fallon, P; Phair, L

    2008-01-09

    The STARS/LiBerACE collaboration has been exploring the surrogate technique with success in the actinide region. This method uses a direct reaction to measure the decay probability of the same compound nucleus produced via a neutron-induced channel. This paper serves as an overview of these activities. Using the STARS array at 88-inch Cyclotron at Lawrence Berkeley National Laboratory we have explored the following surrogate reactions: {sup 234}U({alpha}, {alpha}{prime}f), {sup 235}U({sup 3}He, {alpha}f), {sup 236}U({alpha}, {alpha}{prime}f), {sup 238}U ({alpha},{alpha}{prime}f), {sup 238}U({sup 3}He,{alpha}f), {sup 238}U({sup 3}He, tf) surrogates for {sup 233}U(n,f), {sup 233}U(n,f), {sup 235}U(n,f), {sup 237}U(n,f), {sup 236}U(n,f), and {sup 237}Np(n,f), respectively.

  16. Estimation of (n,f) Cross-Sections by Measuring Reaction Probability Ratios

    Energy Technology Data Exchange (ETDEWEB)

    Plettner, C; Ai, H; Beausang, C W; Bernstein, L A; Ahle, L; Amro, H; Babilon, M; Burke, J T; Caggiano, J A; Casten, R F; Church, J A; Cooper, J R; Crider, B; Gurdal, G; Heinz, A; McCutchan, E A; Moody, K; Punyon, J A; Qian, J; Ressler, J J; Schiller, A; Williams, E; Younes, W

    2005-04-21

    Neutron-induced reaction cross-sections on unstable nuclei are inherently difficult to measure due to target activity and the low intensity of neutron beams. In an alternative approach, named the 'surrogate' technique, one measures the decay probability of the same compound nucleus produced using a stable beam on a stable target to estimate the neutron-induced reaction cross-section. As an extension of the surrogate method, in this paper they introduce a new technique of measuring the fission probabilities of two different compound nuclei as a ratio, which has the advantage of removing most of the systematic uncertainties. This method was benchmarked in this report by measuring the probability of deuteron-induced fission events in coincidence with protons, and forming the ratio P({sup 236}U(d,pf))/P({sup 238}U(d,pf)), which serves as a surrogate for the known cross-section ratio of {sup 236}U(n,f)/{sup 238}U(n,f). IN addition, the P({sup 238}U(d,d{prime}f))/P({sup 236}U(d,d{prime}f)) ratio as a surrogate for the {sup 237}U(n,f)/{sup 235}U(n,f) cross-section ratio was measured for the first time in an unprecedented range of excitation energies.

  17. Flow-injection technique for determination of uranium and thorium isotopes in urine by inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Benkhedda, Karima; Epov, Vladimir N; Evans, R Douglas

    2005-04-01

    A sensitive and efficient flow-injection (FI) preconcentration and matrix-separation technique coupled to sector field ICP-mass spectrometry (SF-ICP-MS) has been developed and validated for simultaneous determination of ultra-low levels of uranium (U) and thorium (Th) in human urine. The method is based on selective retention of U and Th from a urine matrix, after microwave digestion, on an extraction chromatographic TRU resin, as an alternative to U/TEVA resin, and their subsequent elution with ammonium oxalate. Using a 10 mL sample, the limits of detection achieved for 238U and 232Th were 0.02 and 0.03 ng L(-1), respectively. The accuracy of the method was checked by spike-recovery measurements. Levels of U and Th in human urine were found to be in the ranges 1.86-5.50 and 0.176-2.35 ng L(-1), respectively, well in agreement with levels considered normal for non-occupationally exposed persons. The precision obtained for five replicate measurements of a urine sample was 2 and 3% for U and Th, respectively. The method also enables on-line measurements of the 235U/238U isotope ratios in urine. Precision of 0.82-1.04% (RSD) was obtained for 235U/238U at low ng L(-1) levels, using the FI transient signal approach.

  18. U-Th-Ra disequilibria in sediments of the Dora Baltea river (Italia)

    Science.gov (United States)

    Chabaux, F.; Deloche, A.; Pelt, E.; Granet, M.; Perrone, Th.; Boutin, R.; Viville, D.; Rihs, S.; Stille, P.

    2012-04-01

    In order to constrain the transfer time of sediments in Alpine rivers, we propose to use the U-series nuclides approach recently developed for Himalayan rivers (e.g., Chabaux et al., 2008; Granet et al., 2010). Therefore, a series of bank sediments has beeen collected along the Dora Baltea river (Italia), one of the Po's tributaries draining the southern slope of the Mont Blanc Massif. In addition to U series nuclides, major and trace element concentrations and Sr and Nd isotope ratios have been analyzed for each sample. The study indicates that the (234U/238U)-, (230Th/234U)- and the (226Ra/230Th)- activity ratios are very similar for all the samples, whereas the 230Th/232Th ratios can differ from one sample to another. Such a variation, consistent with the Sr and Nd isotope data, is certainly the consequence of mineralogical heterogeneities in the samples. This suggests that the use of 238U-230Th-232Th systematics alone is probably insufficient for constraining the transfer time of sediments in the Po rivers alluvial plain, whereas the combination of 238U-230Th disequilibrium with the 230Th-226Ra disequilibrium can help to constrain such time information.

  19. Radionuclide Determination In Surface Water Samples By Inductively Coupled Plasma With Sector Field Mass Spectrometry (ICP-SFMS

    Directory of Open Access Journals (Sweden)

    E. T. Romero-Guzmán

    2016-08-01

    Full Text Available The determination of naturally occurring radionuclides in the environment by inductively coupled plasma mass spectrometry of high resolution (ICP-SFMS has gained recognition over the last fifteen years, relative to the radiometric techniques, as the result of improvement in instrumental performance, sample introduction equipment and sample preparation. With the increase in instrumental sensitivity, it is now possible to measure ultratrace levels of many radioisotopes. The aim of this work was to determined the natural radionuclides (232Th, 234U, 235U and 238U in surface water using Inductively Coupled PlasmaSector Field Mass Spectrometry (ICP-SFMS. The samples were sampling from Lerma river, State of Mexico at february to april 2015. The process of treatment of sample consisted in perform an acid digestion according to the 3015A USEPA method followed of the direct measurement in ICP-SFMS. Results obtained were: a identify the presence of 232Th, 234U, 235U and 238U isotopes in water, b isotopic ratios were for 234U/238U=1.133 ± 0.016. ICPSFMS has gained popularity in the field of radiochemistry, particularly as a method of detection for long lived-actinides.

  20. Measurements of reaction rate ratios as indexes of breeding performance in mock-up cores of FCA simulating metallic-fueled LMFBR and MOX-fueled LMFBR

    Energy Technology Data Exchange (ETDEWEB)

    Sakurai, Takeshi; Nemoto, Tatsuo [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Kobayashi, Keiji; Unesaki, Hironobu

    1999-08-01

    Measurements and analysis for reaction rate ratio of {sup 238}U capture to {sup 239}Pu fission (C8/F9) and that of {sup 238}U capture to {sup 235}U fission (C8/F5), which are important as indexes of breeding behavior of a fast breeder reactor, were made at Fast Critical Assembly (FCA) of Japan Atomic Energy Research Institute. The measurements were made by a foil activation technique at two assemblies simulating metallic-fueled liquid metal fast breeder reactor and an assembly simulating a MOX-fueled one. The analysis was made based on JENDL3.2 nuclear data file. Calculation to experiment ratios of C8/F9 and C8/F5 were 0.99-1.02 and 1.0-1.03 respectively. Furthermore, the {sup 238}U capture rate and the {sup 235}U fission rate were measured in a thermal neutron standard field in Heavy Water Facility of Kyoto University Research Reactor to verify accuracy of the present foil activation technique itself and to confirm these C/E values. (author)

  1. Marine anoxia and delayed Earth system recovery after the end-Permian extinction.

    Science.gov (United States)

    Lau, Kimberly V; Maher, Kate; Altiner, Demir; Kelley, Brian M; Kump, Lee R; Lehrmann, Daniel J; Silva-Tamayo, Juan Carlos; Weaver, Karrie L; Yu, Meiyi; Payne, Jonathan L

    2016-03-01

    Delayed Earth system recovery following the end-Permian mass extinction is often attributed to severe ocean anoxia. However, the extent and duration of Early Triassic anoxia remains poorly constrained. Here we use paired records of uranium concentrations ([U]) and (238)U/(235)U isotopic compositions (δ(238)U) of Upper Permian-Upper Triassic marine limestones from China and Turkey to quantify variations in global seafloor redox conditions. We observe abrupt decreases in [U] and δ(238)U across the end-Permian extinction horizon, from ∼3 ppm and -0.15‰ to ∼0.3 ppm and -0.77‰, followed by a gradual return to preextinction values over the subsequent 5 million years. These trends imply a factor of 100 increase in the extent of seafloor anoxia and suggest the presence of a shallow oxygen minimum zone (OMZ) that inhibited the recovery of benthic animal diversity and marine ecosystem function. We hypothesize that in the Early Triassic oceans-characterized by prolonged shallow anoxia that may have impinged onto continental shelves-global biogeochemical cycles and marine ecosystem structure became more sensitive to variation in the position of the OMZ. Under this hypothesis, the Middle Triassic decline in bottom water anoxia, stabilization of biogeochemical cycles, and diversification of marine animals together reflect the development of a deeper and less extensive OMZ, which regulated Earth system recovery following the end-Permian catastrophe.

  2. Rapid expansion of oceanic anoxia immediately before the end-Permian mass extinction.

    Science.gov (United States)

    Brennecka, Gregory A; Herrmann, Achim D; Algeo, Thomas J; Anbar, Ariel D

    2011-10-25

    Periods of oceanic anoxia have had a major influence on the evolutionary history of Earth and are often contemporaneous with mass extinction events. Changes in global (as opposed to local) redox conditions can be potentially evaluated using U system proxies. The intensity and timing of oceanic redox changes associated with the end-Permian extinction horizon (EH) were assessed from variations in (238)U/(235)U (δ(238)U) and Th/U ratios in a carbonate section at Dawen in southern China. The EH is characterized by shifts toward lower δ(238)U values (from -0.37‰ to -0.65‰), indicative of an expansion of oceanic anoxia, and higher Th/U ratios (from 0.06 to 0.42), indicative of drawdown of U concentrations in seawater. Using a mass balance model, we estimate that this isotopic shift represents a sixfold increase in the flux of U to anoxic facies, implying a corresponding increase in the extent of oceanic anoxia. The intensification of oceanic anoxia coincided with, or slightly preceded, the EH and persisted for an interval of at least 40,000 to 50,000 y following the EH. These findings challenge previous hypotheses of an extended period of whole-ocean anoxia prior to the end-Permian extinction.

  3. Assay methods for U-238, Th-232, and Pb-210 in lead and calibration of Bi-210 bremsstrahlung emission from lead

    CERN Document Server

    Orrell, John L; Arnquist, Isaac J; Eggemeyer, Tere A; Glasgow, Brian D; Hoppe, Eric W; Keillor, Martin E; Morley, Shannon M; Myers, Allan W; Overman, Cory T; Shaff, Sarah M; Thommasson, Kimbrelle S

    2015-01-01

    Assay methods for measuring 238U, 232Th, and 210Pb concentrations in refined lead are presented. The 238U and 232Th concentrations are determined using isotope dilution inductively coupled plasma mass spectrometry (ID-ICP-MS) after anion exchange column separation of dissolved lead samples. The 210Pb concentration is inferred through {\\alpha}-spectroscopy of a daughter isotope, 210Po, after chemical precipitation separation on dissolved lead samples. Subsequent to the 210Po {\\alpha}-spectroscopy assay, a method for evaluating 210Pb concentrations in solid lead samples was developed via measurement of bremsstrahlung radiation from \\b{eta}-decay of a daughter isotope, 210Bi, by employing a 14-crystal array of high purity germanium (HPGe) detectors. Ten sources of refined lead were assayed. The 238U concentrations were <34 microBq/kg and the 232Th concentrations ranged <0.6-15 microBq/kg, as determined by the ICP-MS assay method. The 210Pb concentrations ranged from ~0.1-75 Bq/kg, as inferred by the 210Po ...

  4. Uranium Isotope Ratios in Modern and Precambrian Soils

    Science.gov (United States)

    DeCorte, B.; Planavsky, N.; Wang, X.; Auerbach, D. J.; Knudsen, A. C.

    2015-12-01

    Uranium isotopes (δ238U values) are an emerging paleoredox proxy that can help to better understand the redox evolution of Earth's surface environment. Recently, uranium isotopes have been used to reconstruct ocean and atmospheric redox conditions (Montoya-Pino et al., 2010; Brennecka et al., 2011; Kendall et al., 2013; Dahl et al., 2014). However, to date, there have not been studies on paleosols, despite that paleosols are, arguably better suited to directly tracking the redox conditions of the atmosphere. Sedimentary δ238U variability requires the formation of the soluble, oxidized form of U, U(VI). The formation of U(VI) is generally thought to require oxygen levels orders of magnitude higher than prebiotic levels. Without significant U mobility, it would have been impossible to develop isotopically distinct pools of uranium in ancient Earth environments. Conversely, an active U redox cycle leads to significant variability in δ238U values. Here we present a temporally and geographically expansive uranium isotope record from paleosols and modern soils to better constrain atmospheric oxygen levels during the Precambrian. Preliminary U isotope measurements of paleosols are unfractionated (relative to igneous rocks), possibly because of limited fractionation during oxidation (e.g., {Wang, 2015 #478}) or insufficient atmospheric oxygen levels to oxidize U(IV)-bearing minerals in the bedrock. Further U isotope measurements of paleosols with comparison to modern soils will resolve this issue.

  5. Radium and uranium levels in vegetables grown using different farming management systems

    Energy Technology Data Exchange (ETDEWEB)

    Lauria, D.C. [Instituto de Radioprotecao e Dosimetria (IRD/CNEN), Av. Salvador Allende s/n, Recreio dos Bandeirantes, Rio de Janeiro, RJ, CEP 22780-160 (Brazil)], E-mail: dejanira@ird.gov.br; Ribeiro, F.C.A. [Centro Regional de Ciencias Nucleares (CRCN/CNEN), Av. Prof. Luiz Freire 200, Cidade Universitaria Recife, PE, CEP 50740-540 (Brazil); Conti, C.C. [Instituto de Radioprotecao e Dosimetria (IRD/CNEN), Av. Salvador Allende s/n, Recreio dos Bandeirantes, Rio de Janeiro, RJ, CEP 22780-160 (Brazil); Loureiro, F.A. [Estacao Experimental de Nova Friburgo, Empresa de Pesquisa Agropecuaria do Estado do Rio de Janeiro, Pesagro (Brazil)

    2009-02-15

    Vegetables grown with phosphate fertilizer (conventional management), with bovine manure fertilization (organic management) and in a mineral nutrient solution (hydroponic) were analyzed and the concentrations of {sup 238}U, {sup 226}Ra and {sup 228}Ra in lettuce, carrots, and beans were compared. Lettuce from hydroponic farming system showed the lowest concentration of radionuclides 0.51 for {sup 226}Ra, 0.55 for {sup 228}Ra and 0.24 for {sup 238}U (Bq kg{sup -1} dry). Vegetables from organically and conventionally grown farming systems showed no differences in the concentration of radium and uranium. Relationships between uranium content in plants and exchangeable Ca and Mg in soil were found, whereas Ra in vegetables was inversely correlated to the cation exchange capacity of soil, leading to the assumption that by supplying carbonate and cations to soil, liming may cause an increase of U and a decrease of radium uptake by plants. The soil to plant transfer varied from 10{sup -4} to 10{sup -2} for {sup 238}U and from 10{sup -2} to 10{sup -1} for {sup 228}Ra.

  6. Clay Mineral: Radiological Characterization

    Science.gov (United States)

    Cotomácio, J. G.; Silva, P. S. C.; Mazzilli, B. P.

    2008-08-01

    Since the early days, clays have been used for therapeutic purposes. Nowadays, most minerals applied as anti-inflammatory, pharmaceutics and cosmetic are the clay minerals that are used as the active ingredient or, as the excipient, in formulations. Although their large use, few information is available in literature on the content of the radionuclide concentrations of uranium and thorium natural series and 40K in these clay minerals. The objective of this work is to determine the concentrations of 238U, 232Th, 226Ra, 228Ra, 210Pb and 40K in commercial samples of clay minerals used for pharmaceutical or cosmetic purposes. Two kinds of clays samples were obtained in pharmacies, named green clay and white clay. Measurement for the determination of 238U and 232Th activity concentration was made by alpha spectrometry and gamma spectrometry was used for 226Ra, 228Ra, 210Pb and 40K determination. Some physical-chemical parameters were also determined as organic carbon and pH. The average activity concentration obtained was 906±340 Bq kg-1 for 40K, 40±9 Bq kg-1 for 226Ra, 75±9 Bq kg-1 for 228Ra, 197±38 Bq kg-1 for 210Pb, 51±26 Bq kg-1 for 238U and 55±24 Bq kg-1 for 232Th, considering both kinds of clay.

  7. Preliminary Study of Natural Radioactivity in the Lake Bosumtwi Basin

    Directory of Open Access Journals (Sweden)

    Simon Adu

    2011-08-01

    Full Text Available The concentrations of 238U, 232Th, and 40K in water from Lake Bosumtwi and bore-holes in selected towns around the Bosumtwi basin of the Ashanti region of Ghana have been determined. The concentrations were determined for water samples from 24 boreholes and 12 points across the lake using a High-Purity Germanium (HPGe (γ-ray spectrometry. The water samples from the lake were found to contain acceptable levels of radionuclides with mean activity concentrations of 7.9, 89.7 and 0.6 mBq/L for 238U, 40K, and 232Th, respectively. The water samples from the boreholes recorded mean activity concentrations of 7.7, 85.5, and 3.3 mBq/L for 238U, 40K and 232Th, respectively. The annual effective dose calculated for the lake varied from 0.244 to 1.121 μSv with an average of 0.763 μSv and that calculated for the boreholes varied from 0.296 to 2.173 μSv with an average of 1.166 μSv. The radionuclides concentrations in water from the bore-holes and that of the lake, which serve as sources of water supply to the surrounding communit